Professional Documents
Culture Documents
Hydrochloric acid
Flinn Chemicals 6M solution
Are Always Corrosive to all body tissue,
especially skin and eyes.
Properly Labeled! Avoid all body contact.
2001
The NFPA code is a numerical code © 2002 Flinn Scientific, Inc . All Rights Reserved . PAGE 1 Of 2
established by the National Fire
Protection Associate. It rates the
substance under fire conditions in four
categories. Health, Flammability,
Reactivity, and unusual reactivity: 4 is a How can I prevent hazardous situations from occurring?
severe hazard, 0 is no hazard.
Sections 7-11.
How to clean up a spill. Always Use the Flinn Suggested Chemical Wear personal protection equipment
remove unprotected personnel from area Storage Pattern to prevent accidents and such as goggles, gloves, and an apron.
and make sure all students are safe. improve safety. Special storage and See page 928 for an explanation on TWA
Contain the spill with sand or absorbent usage tips are also included. and STEL.
materials.
Each Flinn MSDS follows the same format and the data is always found in the same location making it a valuable resource in the
event of an emergency. Flinn sends an MSDS with every chemical you order. Flinn MSDS are continually updated, guaranteeing the
most up-to-date safety information possible. Flinn sells a complete MSDS library in two versions, a hard copy version in two binders
or an electronic version on a CD-ROM. For a more detailed description of our MSDS Library, please refer to pages 908-909. For ou r
customers' convenience, Flinn has placed a complete set of MSDS on our website. Simply go to www.flinnsci.com and click on the
safety icon-individual MSDS are easy to find and very easy to print out on your printer.
N.A. :::: Not avai lable, not all health aspects of thi s substance have been fully in vestigated. Oral (ORL), inhalation (IHL), and skin
absorption (SKN) toxicity data on test
animals is included. For more information
Data not yet available.
on LDso and LC so , see page 930.
Chemical Exposure
When Are Vapors Harmful
To You and Your Students?
Threshold Limit Values (TLV) and Permissible Exposure The best practice is
Limits (PEL) refer to the level of a chemical above which to maintain concentra-
a person should avoid repeated and prolonged expo- tions of all atmospheric
sure. TLVs and PELs were originally structured to provide contaminants to the
guidelines for workers in industry who are repeatedly lowest practical levels.
exposed to the same chemicals day after day. Science There are three primary steps
teachers can use these values to provide guidance on that will help reduce your expo-
which chemicals to use and when to take precautions. sure to volatile or other airborne
TLVs and PELs are very general standards since every chemical substances.
individual responds differently to exposure. The amount of 1. Ventilation. Ventilation of the school science labora-
exposure and the time period of exposure are the critical tory should be of paramount importance to the science
issues. teacher. Two types of ventilation should be incorpo-
The difference between TLVs and PELs is the agen- rated in the science laboratory. A purge ventilation
cies from which they come. TLVs are developed by the system (see page 919) should be available to provide
American Conference of Governmental Industrial a quick air exchange in the laboratory whenever
Hygienists (ACGIH). PELs are developed by the the level of hazardous chemical vapors or dust
Occupational Safety and Health Administration (OSHA). approaches the TLV. Also, fume hoods should be
They both serve the same purpose and their values are available and used whenever volatile and hazardous
very similar or even identical in many cases. For the materials are used. A reaction that is performed in a
remainder of this article, we will refer only to TLVs. properly operating fume hood will not release any
TLVs for vapor or gas are reported as parts per million vapors into the laboratory.
(ppm) or milligrams per cubic meter (mg/m3) of air. A 2. Substitution. Use the TLV table on the following page
cubic meter is approximately the size of a small tele- to substitute a less hazardous chemical for the exper-
phone booth. Dust , Rarticulate matter, or mist are iment or activity. For example, if an alcohol is required
reported only as milligrams per cubic meter of air. for an experiment and methyl, ethyl, or isopropyl alco-
Many substances have effects which are acute and hol can be used, the smart choice is to use ethyl
fast-acting. A ceiling limit has been established for these alcohol because it has the highest TLV. Another exam-
items. This ceiling suggests that the limit not be exceeded ple is melting point determinations. Many teachers
even for an instant. For example, the ceiling TLV for iodine have used naphthalene or para-dichlorobenzene, both
is 0.1 ppm or 1 mg/m 3. of which have a TLV of 10 ppm. Why not substitute a
less hazardous material such as cetyl alcohol, stearic
For those chemicals that are acute or fast-acting
acid, or t-octyl phenol?
through skin absorption, gloves must be worn; the
substances must also be handled in either an operating 3. Microscale. Scaling down the quantity of material
fume hood or a well-ventilated room. used will reduce the amount that can volatilize into
the atmosphere. If a typical class (15 lab groups, 280
The threshold of smell of many chemicals is usually
m3 room) performs a lab where sulfur is burned to
below that of the TLV. Strong smell may act as a warning
form sulfur dioxide and the lab is microscaled to use
that the TLV is being approached. Since human smelling
only 0.05 g of sulfur, the average level of sulfur dioxide
ability can be impaired by some odors, one should not
in the room would not exceed 3 mg/m 3, below the TLV
depend on smell as a reliable indicator of a hazard.
of 5.2 mg/m 3. However, if 0.2 g or more are used by
Chlorine gas, as an example, has a TLV of 0.5 ppm or 1.5
each group, the TLV would quickly be exceeded.
mg/m3. Your odor threshold for chlorine is likely to be 0.3
ppm. If you can smell it, you are probably at or near the TLVs are not well-defined limits between what is safe or
level of concern. unsafe. Rather, they should be used as guidelines to the
teacher. Most students are in the laboratory for only short
Biology teachers particularly should note the very low periods each week. The teacher's exposure is, of course,
TLV for formaldehyde (0.3 ppm) and either plan to eliminate much greater. Following the above steps will greatly
formaldehyde from their program, use it only under reduce your exposure to hazardous chemicals.
a hood, or be sure the room air in their laboratory is The following is a list of common school laboratory
being changed (not recirculated) a minimum of 10-12 times chemicals and their TLV values. This is not a comprehen-
per hour. Fortunately, many preserved materials now sive listing. TLV values are subject to change as new
contain only very small amounts of free formaldehyde. information is developed.
Acetic Anhydride' 5 21 Chromates and Dichromates - 0.05 Methyl Chloroform 350 1910
Acetone 750 1188 Chromium (III) Compounds - 0.5 Methyl-t-Butyl Ether 40 144
Alu mina' - 10 Chromium Metal and - 0.5 Methyl Ethyl Ketone 200 590
Insoluble Salts
Aluminum Metal' - 10 Methyl Isobutyl Ketone 50 205
Cobalt - 0.02
Am monia 25 17 Methyl Methacrylate 100 410
Copper' - 1
Am monium Chloride' - 10 Naphthalene 10 52
Cyclohexane 300 1030
Am monium Dichromate' - 0.5 Nicotine' - 0.5
Cyclohexanol' 50 206
n-Amyl Acetate 100 532 Nitric Acid 2 5.2
Cyclohexanone' 25 100
Ani line and Homologs' 2 7.6 Oxalic Acid - 1
Cyclohexene 300 1010
Antimony and Compounds - 0.5 Pentane 600 1770
p-Dichlorobenzene 10 60
Arsenic and Soluble Compounds - 0.01 Phenol' 5 19
Dioxane' 25 90
Barium and Barium Compounds - 0.5 Phosphorus 0.02 0.1
Ether, Ethyl 400 1210
Barium Sulfate - 10 Phthalic Anhydride' 1 6.1
Ethyl Acetate 400 1440
Benzene 0.5 1.6 Potassium Hydroxide' - 2
Ethyl Alcohol 1000 1880
Benzoyl Peroxide - 5 Propane 2500 4508
Ethylenediamine' 10 25
Bromine and Bromine Water 0.1 0.66 n-Propyl Alcohol' 200 492
Ethylene Dichloride' 10 40
Bromoform 0.5 5.2 Pyridine 5 16
Ethylene Glycol' - 100
Butane 800 1900 Silver Nitrate - 0.01
Formaldehyde 0.3 0.37 (as silver)
2-Butanone 200 590
Formic Acid 5 9.4 Sodium Bisulfite - 5
n-Butyl Alcohol '" 50 152
n-Heptane 400 1640 Sodium Hydroxide' - 2
sec-Butyl Alcohol 100 300
n-Hexane 50 176 Styrene' 50 213
tert-Butyl Alcohol 100 303
Hydrochloric Acid' 5 7.5 Sulfur Dioxide (gas) 2 5.2
Cadmium and Cadmium - 0.01
Compounds' Hydrogen Fluoride' 3 2.3 Sulfur Hexafluoride 1000 5970
Carbon Dioxide 5000 9000 Isopropyl Alcohol 400 983 Trichloroethylene 50 269
Carbon Disulfide' 10 31 Lead , Metal and Compounds' - 0.05 Turpentine 100 556
Substance LD50 Oral-rat per kilogram Substance LD50 Oral-rat per kilogram Substance LD50 Oral-rat per kilogram
Acetaldehyde ............. .......... .... ... .. ...... 661 mg n-Butyl Alcohol .................. ................. 790 mg Cuprous Chloride .. .... .. ...... .. .. .. ...... .. .. . 140 mg
Acetamide ............................... ... .. ..... 7000 mg sec-Butyl Alcohol .. ........................... 6480 mg Cuprous Oxide ............... .. ............ ...... 470 mg
Acetanilide .......... ............... .. ... .. .... .. .. .. 800 mg tert-Butyl Alcohol .. .. ................. ...... .. .3500 mg Cyclohexane .. .. .. ..... .. .. .... .. ... .. .. .. ..... 12705 mg
Acetic Acid .......................... ......... ..... 3310 mg Butyl Phthalate .. ............................... 8000 mg Cyclohexanol .................... .. .... .... ...... 2060 mg
Acetic Anhydride .... .. ... ... .. ................ 1780 mg Butyric Acid ......................... ............. 2000 mg Cyclohexene ... ................. .. ...... .. ....... 2300 mg
Acetone ...... .. .............................. ...... 5800 mg Cadmium ............... .. ........................... 225 mg 2,6-Di-t-Butyl-4-Methyl Phenol .. ...... .. 890 mg
Acetyl Salicylic Acid ........ ... ... .. ...........200 mg Cadmium Chloride ...... .........................88 mg p-Dichlorobenzene ............................. 500 mg
Adenine ............................ ................... 745 mg Cadmium Nitrate .... ............... .... ..... .... 305 mg 2,4-Dichlorophenoxy Acetic Acid ...... 375 mg
Aluminum Chloride .. .. .. .. .. ................. 3310 mg Caffeine ... ................. ... ....... .. ............... 192 mg Diisopropanolamine .. .. .......... ... .. ..... ..6720 mg
Aluminum Nitrate .. .. .. ...... ................ .. 3671 mg Calcium Chloride ..............................1000 mg 1,4 Dioxane .. .. .. ................. .. .. .. .......... 5700 mg
Ammonium Chloride ............. ............ 1650 mg Calcium Fluoride .... .. .. .. .. .. .. .. ............ .4250 mg Diphenylamine ............ .. .. ...... .. ......... ... 300 mg
Ammonium Hydroxi de .... .................... 350 mg Calcium Hydroxide .... ............. .. ...... .. 7340 mg Dodecyl Alcohol .. .................... ....... 12800 mg
Ammonium Molybdate .......................333 mg Calcium Hypochlorite .............. ........... 850 mg Ethyl Acetate ...... .. .. ..... .. .. ... .............. 6100 mg
-
Ammonium Nitrate .... ................ .. .... .2217 mg Calcium Nitrate .................... .. .. ......... 3900 mg Ethyl Alcohol .. .. .... .. .. ......................... 7060 mg
Ammonium Persulfate .... .................... 689 mg Carbon Disulfide ...............................3188 mg Ethyl Ether ............ ............................ 1215 mg
Ammonium Sulfate ........................... 2840 mg Carbon Tetrachloride ...... .. ................ 2800 mg Ethylene Diamine .............. ... ..... .......... 500 mg
Ammonium Thiocyanate ...... .. .. .. .... .. .. 750 mg Cesium Chloride .. .. .... .. ... ...... .. .. .... .... 2600 mg Ethylene Dichloride ........ .. ..... .... .... .... .. 670 mg
Amyl Acetate .. .. .... .......... .. ................ 6500 mg Cetyl Alcohol ........................ .. .. ..... ... 5000 mg Ethylene Glycol .. .............. .. .. .. .. ........ .4700 mg
n-Amyl Alcohol ...................... .......... .2200 mg Chloroform .. .. .. ..... ............ .. .. .. .... ..... .. ..908 mg Ferric Chloride .. ................ .. .............. 1278 mg
Ani line ................................................. 250 mg Ferric Nitrate ...... .... .......... ................. 3250 mg
Aniline Hydrochloride .... ....... .. ............ 840 mg Never ingest any laboratory Ferrous Sulfate .. ................... ............ 1520 mg
Antimony ... ..... .... .. ............ ................ .7000 mg chemical, no matter the LDso. Formaldehyde ........ .... ...... ...... .. ........... 100 mg
Antimony Trichloride .. .... ..................... 525 mg Formic Acid ............... .. .. .......... .........1100 mg
Arsenic Trioxide ............................... .. 15.1 mg Chromium(ic) Chloride ...................... 1790 mg Fumaric Acid ......... .... .. .. .. ......... .. .... 10700 mg
Barium Acetate .... .. ................. .. .......... 921 mg Chromium(ic) Nitrate .... .. .. ... .. .. .... .. .... 3250 mg Glutaraldehyde .................. ................ .134 mg
Barium Carbonate ................ ...... .. ..... .418 mg Chromium Trioxide .... .... ............ .. ......... 80 mg Glycerin ........................... .. ........ ..... .12600 mg
Barium Chloride ...... .. .. .................... .. .. 118 mg Cinnamaldehyde ... ... ... .... .. ................ 2220 mg Hexamethylenediamine ...... .... .... .... .... 750 mg
Bari um Nitrate ... ............ .. .. .... .. ...... .. .. .. 355 mg Citric Acid ......................... ... .......... .11700 mg Hexanes .......... ........... ....... .. .. .......... 28710 mg
Benzaldehyde .. .......................... ....... 1300 mg Cobalt Carbonate ............ ... .. .............. 640 mg Hexyl Alcohol .. ....... .... .. .................... .. .720 mg
Benzene ....................... .. .................. .4894 mg Cobalt(ous) Chloride ........................... 766 mg Hydroquinone .......... .................. ......... 320 mg
Benzoic Acid .............. ....................... 1700 mg Cobalt(ous) Nitrate .. ................ .. ...... .. .. 691 mg Hydroxylamine Hydrochloride .. .... .. .... 408 mg
Benzoin .. .. .... .. .... .. .... ............ .. ...... ... 10000 mg Cobalt Oxide .... ............. .. .. .. .. .. ... ....... 5000 mg Indigo Carmine ............ ....... .. ............ 2000 mg
Benzoyl Peroxide .. .. .................. .. ...... 771 0 mg Cobalt(ous) Sulfate ............... .. .... .... .. .. 768 mg 3-lndole Butyric Acid ......... .. .. ...... .... .. .100 mg
Benzyl Alcohol ........ .... .. .. .. ...... .. ........ 1230 mg Colchicine .............. ........ .. ... ...... .. ....... ..... 6 mg Iodine ...... ... ................ .... ......... ... ..... ..4000 mg
Benzyl Benzoate .............. .. .. .. .. .. .... .. .. 500 mg Crystal Violet.. ..................... .... .. .... ...... 420 mg Isobutyl Alcohol .... ...... .. .. .. ...... .. ........ 2460 mg
Bismuth ................... ... ...... .. ........... .. ..5000 mg Cupric Acetate ..... .. ..... .. .. .. .. .. ......... ..... 710 mg Isopropyl Alcohol .............. .. .... .. ........ 5045 mg
Bismuth Nitrate ....... .. ....... .. ............ ... 4042 mg Cupric Carbonate ....... .. .. ...... ............ 1350 mg Isopentyl Alcohol .... .... .. ...... .. .. .. ........ 1300 mg
Boric Acid ......................................... 2660 mg Cupric Chloride .. .. .. ..... .. .. .. .. .. .. .... ........ 140 mg Lactic Acid .............. .. ...... .. .. .. .. .. ........ 3730 mg
Bromobenzene .................. ............... 2699 mg Cupric Nitrate .. ..................... ...... ........ 940 mg Lauric Acid .................. .. .. .. .............. 12000 mg
Bromoform ..................................... ... 1147 mg Cupric Sulfate ... ...... .. .. .. .. .. .. .. ... .... ....... 300 mg Lithium Carbonate .......... .... .. .. .. .......... 525 mg
Substance LD50 Oral-rat per kilogram Substance LD50 Oral-rat per kilogram Substance LD50 Oral-rat per kilogram
Lithium Chloride ...................... ...... .. ... 526 mg Potassium Iodate ............... .. ... ... ... ..... 53 1 mg Sodium Silicate, meta ... ..... .. .. .......... 1153 mg
Lithium Sulfate ......... ....... .... .... ... .... .. .1190 mg Potassium Nitrate ... .... ... .... .. .. .......... 3750 mg Sodium Sulfite .......................... ..... .. ... 820 mg
Magnesium Chloride ...... ............. .....2800 mg Potassium Nitrite ............................... 200 mg Sodium Thiocyanate ......... .... .... .......... 764 mg
Magnesium Nitrate .. .. ....... ....... ... ......5440 mg Potassium Permanganate ......... ....... 1090 mg Stannous Chloride ............ .. .. ........ ... ... 700 mg
Malachite Green Oxalate .................... 275 mg Potassium Persulfate .............. ... ......... 802 mg Strontium Nitrate ... ............ ............... 2750 mg
Maleic Acid ......................................... 708 mg Potassium Phosphate, Tribasic ....... .1450 mg Styrene ...... .. ............. ....... .................. 5000 mg
Maleic Hydrazide ............ ........ ......... .3800 mg Potassium Thiocyanate ................... ... 854 mg Succinic Acid .............. .... ... ........ ...... .2260 mg
Malonic Acid .................................... 1310 mg Propionic Acid ........... ............ ........... 2600 mg Sulfamic Acid ....................................3160 mg
Manganous Chloride .. .... ... ... .. .. ....... .1984 mg n-Propyl Alcohol ............................... 1870 mg Sulfanilamide .............. ... .... ............... 3900 mg
Mentho!. ....... ....... .. ........ .. ....... ... .......3180 mg Pyridine .. .......... .. .. ............................... 891 mg 5-Sulfosalicylic Acid ... .. ....... ............. 2450 mg
Mercuric Chloride .. ..... ..... .. ..... .. 1 mg Pyrogallol ...... ..... ...... ... ... ....... .. .. .... 300 mg
Mercuric lodide ... ............ .... ...... ........... .40 mg Resorcinol ........ ........ ... ........................ 301 mg To put toxicity into perspective,
Mercuric Nitrate .................................... 26 mg Rhodamine B ........ ............................. .887 mg compare the LD50 to that of
Mercuric Oxide ..... .. .............................. 18 mg Salicylic Acid ............................. ......... 891 mg sodium chloride (3000 my).
Mercuric Sulfate ...... ...... ...... ... ..... ......... 57 mg Silver Nitrate ....... .. .... .... .. .. .. .. ................ 50 mg
Mercurous Chloride .. .......................... 166 mg Silver Oxide .................. .. ..... ... .......... 2820 mg Tannic Acid .. .................................... .2260 mg
Mercurous Nitrate .. ......... .... ................ 170 mg Soda Lime ............................ ...... ......3530 mg Tetrahydrofuran ...... .. ... ..................... 2500 mg
Mercurous Sulfate .............................. 152 mg Sodium Arsenite .............. ... ................. .41 mg Thioacetamide ...... ................ .............. 301 mg
Methyl Alcohol .................................. 5628 mg Sodium Azide ...................................... .27 mg Thiourea ............ ........ ..... ... ... .. .. ... .. .. .... 125 mg
Methyl-t-Butyl Ether ... ... ... ................ 3865 mg Sodium Bisulfite .................... ... ........ 2000 mg Thymol ......... .... .... ............ .... ... ............ 980 mg
Methyl Ethyl Ketone ................. ........ 2737 mg Sodium Borate ............... .... .. .. ..... .. .... 2660 mg Toluene ............................................. 636 mg
Methyl Isobutyl Ketone ....... .... .......... 2080 mg Sodium Bromate .... ... .. .. .... ................ .300 mg Trichloroacetic Acid ... .. .400 mg
Methyl Methacrylate ......................... 7872 mg Sodium Bromide ........................... .. 3500 mg 1,1,1 Trichloroethane ....... 10300 mg
Methyl Orange ........................... ... .. ..... .60 mg Sodium Carbonate .................. .. .... ..4090 mg Trichloroethylene .................... .. ....... 2402 mg
Methyl Salicylate ..... ... ... ... ............ ....... 887 mg Sodium Chlorate .......... .. ............. .. .... 1200 mg 1,1,2 Trichloro Trifluoroethane ... .... .43000 mg
Methyl Violet .............. .... .... ................ .413 mg Sodium Chloride ................ .............. 3000 mg Triethanolamine ......... ........ ......... ... .. .8680 mg
Methylene Blue ....................... .......... 1180 mg Sodium Chromate ........................ ........ 52 mg Tris-(Hydroxymethyl)
Methylene Chloride ............. .... 1600 mg Sodium Cyanide ............ ..... .... .. .. .. ..... 6.4 mg Aminomethane ........... ................ ..... 5900 mg
Napthalene .... ............................. ....... .490 mg Sodium Dichromate ............. ... ... ..... ..... 52 mg Uranyl Nitrate ......... ....... ... ... ................ 12 mg
1-Napthol .. ........................................ 1870 mg Sodium Fluoride .................................. 52 mg Urethane ............................. ........... 1800 mg
Nickel(ous) Chloride ............ ......... 105 mg Sodium Iodide ........ .. ....................... 4340 mg Xylenes ........... ... ......... ..... ................ .4300 mg
Sodium Nitrate ... .. .... ................ ....... .. 3236 mg Zinc Acetate .. ... .... .. ........ ... ... .............. .794 mg
III
Nickel(ous) Nitrate ... ..... .................... 1620 mg
Nickel(ous) Sulfate ......... .................... .275 mg Sodium Nitrite ... ............ ............. ........... 85 mg Zinc Chloride ..... ............. ................ 350 mg
Nicotine ....................... .......... ... ..... .. ... .. 50 mg Sodium Perborate ... .......... ............... 1200 mg Zinc Nitrate ............... ... .... .. ... ............ 1190 mg
para-Nitrophenol ............... ................. 250 mg Sodium Phosphate, Tribasic ............ 6500 mg Zinc Oxide ............... ......... .................. 630 mg
1-0ctadecanol ................................20000 mg Sodium Salicylate .. ........................... 1200 mg Zinc Sulfate ... ................ .... .. ........... .. .2150 mg
1-0ctanol .... ... .. .. .. .... ..... .... ... .... .. .. ..... 1790 mg
4-(t-Octyl) Phenol ...... ...... .. .. ...... ... .... 3210 mg
Orcinol ....................... .... ........ ............. 844 mg
Oxalic Acid ..................................... .... 375 mg
Perchloroethylene ... ..... .... ................. 1100 mg
1,1O-Phenanthroline ... ........................ 132 mg Safer Storage
Phenol ........... .. ......................... ....... .... 384 mg
Provide an extra safety edge for the
1 A -Phenylenediamine ......... ................. 80 mg storage of severe poisons. Chemicals
Phenyl Salicylate ......................... .. ... 3000 mg that have an LDse of less than 250 mg
Phenyl Thiocarbamide ............. ............... 3 mg should be stored in a separate and
Phosphoric Acid .. ... .. .. .. .. .... ....... ....... 1530 mg secure storage cabinet to protect
Phosphorous, yellow ..... .................. ... .1.4 mg against theft, vandalism, or fire.
Phosphorous Pentoxide ................. .... 660 mg The Flinn/SciMatCo Poison Cabinet is
Phthalic Anhydride ................ .......... .4020 mg compact; it fits into an existing storage
Potassium Bisulfate .......................... 2340 mg cabinet or shelf.
Potassium Bromate ............................ 321 mg
Severe poisons must be locked up. The
Potassium Carbonate ....................... 1870 mg
Flinn/SciMatCo Poison Cabinet is a
Potassium Chloride .......... .. ... .. ... .... .. 2430 mg "must" safety aid for any high school
Potassium Chromate ....................... ... 180 mg chemical storage area.
Potassium Cyanide ....................... ....... 10 mg
Potassium Dichromate ...... .............. ..190 mg Catalog No. Description Price/Each
Potassium Ferricyanide .......... .. .. ..... .1600 mg
SE6080 Flinn/SciMatCo Wooden Poison Cabinet $324.00
Potassium Ferrocyanide ........... .. .... .. 3613 mg
Potassium Fluoride .... ........ ................ .245 mg See page 876 for more information.
Potassium Hydroxide ............... ...... .... 273 mg
FLI"" ,SCIE"TIFIC I"C. ________"Yc_o_ur_S_a"_er_S_O_Uf_Ce_ "_Or_S_CI_·en_C_e _Su_p...p'_ie_s"
-----------------------------
• Instruct students to remove only the
solvents, the major hazards are flam-
mability and inhalation. If there is a spill
or accident , immediately remove any
kept separate from aqueous wastes to
prevent any accidental reactions. For
organic waste containers, it is best to
amount of flammable liquid needed for flames, heat, or electrical equipment separate halogenated organic solvents
the experiment from the reagent bottle. from the area and begin to ventilate (e.g. , methylene chloride) from other
Never add chemicals back to reagent the area. organic solvents (e.g., ethyl alcohol) for
bottles. • If an organic liquid is splashed in the disposal reasons. Sometimes, volatile
eyes, use an eyewash to irrigate the organic solvents can be evaporated in a
• Have spill c leanup materials readi ly
eyes with fresh , potable water for at fume hood from the organiC waste
available whenever flammable liquids
least 15 minutes. Make sure the eyelids container. Be sure to label all waste
are used. If a spill occurs, immediately
are held open to properly irrigate them. containers with their approximate
restrict unprotected personnel from the
Ask the victim to look up, down, and contents. Dispose of all waste solutions
area, remove all ignition sources, and
sideways to better reach all parts of the as soon as possible.
ventilate the area. If the spill is too large
FLI"" ,SCIE"TIFIC I"C. ________'_'yo_u_r _Sa_fe_r_S_ou_rc_e_fo_r_S_ci_en_c_e _Su....p...pl_ie_s"
Acid Safety
Safety Tips for Using Acids in School Laboratories
Introduction years of safe and durable acid storage.
The use of acids is an important The cabinet should be located in a
component of most chemical laborato- locked chemical storeroom. If not, the
ries. Understanding the properties and cabinet must be secured with a lock.
hazards of acids are important initial • Storing acids and bases together in
steps to safe purchase, storage, use, one corrosive cabinet is acceptable.
and disposal of acids. However, the bottles may become
covered with ammonium chloride from
Safety Precautions the hydrochloric acid and ammonia
Concentrated acids are strongly corro- fumes . The cabinet and bottles should
sive to all body tissue, especially eyes be washed with TSP or other strong
and skin. Concentrated acids are highly cleaners to remove the white film .
toxic due to their extreme corrosiveness.
.If an acid cabinet in not available , hydrochloric acid in a wood acid cabi-
Hydrochloric and acetic acids are also
toxic by inhalation . Other hazards are store concentrated acid in Flinn net is a must. Hydrochloric acid fumes
Saf-Cubes®. A Saf-Cube will provide will quickly corrode metal cabinets.
presented in this review. Always wear
chemical splash goggles , chemical- good secondary containment and
• Nitric acid is a strong oxidizing agent.
resistant gloves , and a chemical- protection.
Concentrated nitric acid must b e
resistant apron whenever using con- • Label all prepared acid solutions before stored in a separate liquid-tigh t
centrated acids or acid solutions. storing them with at least the name of compartment within an acid cabinet. If
the acid , concentration , hazard warn- nitric acid is mixed with a flammable
Purchase ing or how the acid can hurt you , and organic compound , such as aceti c
• Purchase dilute acids whenever possi- date prepared on the label. acid , the heat from the oxidation and
ble. Dilute acid solutions are safer, and neutralization reactions is enough to
• Always keep the appropriate color-
easier to handle, use, and store than coded acid bottle cap on the ignite the flammable material. Nitric
concentrated acids. They will also save concentrated acid bottle. Never use acid also slowly destroys its red plastic
valuable prep time. these caps on other bottles. Color- bottle cap. Always replace with a new
• Purchase small quantities of acids to coded bottle caps provide an extra red cap. Nitric acid may also tu rn
help keep your acid fresh and to make safety measure to identify concen - yellow over time because of the release
storage and handling safer and easier. trated acids if the label is removed or of nitrogen dioxide on exposure to
It is easier to clean up a 1OO-mL than a destroyed . If an acid bottle cap light. The yellow color does not affect
2.5-L acid spill. becomes cracked or discolored , the product's usefulness in the school
• Always purchase concentrated acids in always replace the cap with the proper laboratory.
PVC-coated glass bottles. PVC-coated color-coded cap. The following colors • Glacial acetic ac id is a flammab le
bottles will not shatter and spill acid are used on all concentrated acid liquid. It should be stored in an acid
when dropped. The PVC creates a plas- bottles sold in the United States. cabinet, but in a location isolated from
tic envelope around the bottle that • Acetic Acid - Brown possible contact with nitric ac id .
greatly reduces spills and breakage. The Glacial acetic acid freezes at 16.6 °C;
• Phosphoric Acid - White
PVC coating may discolor over time, the material may crystallize in a cool
especially when exposed to hydrochlo- • Hydrochloric Acid - Blue storeroom . If this occurs , allow the
ric acid fumes. This discoloration does • Sulfuric Acid - Yellow bottle to warm up to ambient (25 °C)
not affect the PVC coating or the qual- • Nitric Acid - Red temperature.
ity of the acid inside the bottle. • Concentrated sulfuric acid is a strong
• Ammonium Hydroxide - Green
Storage dehydrating agent. Because of its
• Concentrated hydrochloric acid fumes
strong ability to remove water, it reacts
• Store all acids in a dedicated corrosives continuously and cannot be stored
violently with many organic materials
or acid cabinet. The best acid cabinets without releasing hydrochloric acid
such as sugar, wood , and paper. If
are built with wood because metal fumes. These fumes are responsible
sulfuric acid has turned brown , it has
cabinets will quickly corrode from acid for most of the corrosion damage in
fumes. Wood cabinets will provide your chemical storeroom. Storing ACID SAFETY continued on next page.
Properties
Concentrated Acid
F.W. Specific
Acid Formula g/mol Gravity wt% Acid Molarity
Acetic HC 2 H3 0 2 60.05 1.05 99.8 17.4
Hydrochloric HCI 36.46 1.19 37.2 12.1
Nitric HN03 63.02 1.42 69.5 15.8
Phosphoric H3 P0 4 98.00 1.70 86 14.8
Sulfuric H2SO 4 98.08 1.84 96 18.0
1-800-452-1261 Acid Safety
ACID SAFETY, continued 6. Use a volumetric flask for extra preciSion. are used. Safety glasses are not
7. When diluting sulfuric acid , place the adequate protection.
probably been contaminated with an borosilicate beaker or flask in an ice • Good ventilation should be available
organic material and its purity should bath. The heat of dilution of sulfuric whenever hydrochloric, nitric, or acetic
be in question. acid is very high and may melt plastic acids are used.
• Concentrated phosphoric acid has a containers or crack non-borosilicate • Spill control materials (sand, absorbent,
melting point close to ambient temper- glassware. and neutralizer) must be available when-
ature and may also crystallize in a cool ever acids or acid solutions are used .
storeroom . Phosphoric acid is hygro-
scopic and will absorb water over time. Always add acid to water ... First Aid
Keep tightly sealed. • Always seek professional medical
attention upon exposure to an y
Transporting USing and DispenSing Acids hazardous chemical , especially
• Secondary containment is critical to • Always review the Material Safety Data concentrated acids.
prevent major spills or accidents when Sheet (MSDS) before using an y
transporting acids. Use PVC-coated • The best first aid for any chemical
hazardous material in the laboratory. exposure to body tissue or eyes is
acid bottles or unbreakable bottle
• Students should dispense acids from immediate dilution with water.
carriers .
smaller bottles to limit spills and fumes. • If an acid is splashed in the eyes, use
• A good habit is to check the acid bottle
• Use lab mats and or plastic trays when an eyewash to irrigate the eyes for at
for cracks before touching or picking it
dispensing acids to contain acid spills least 15-20 minutes. Make sure the
up. Also check for spilled acid on the
and drips. eyelids are held open to properly irri-
handle or bottle.
gate them . Ask the victim to look up,
• Always carry 2.5-L acid bottles with • Dispense acids, especially hydrochlo-
down , and sideways to better reach all
one hand underneath the bottle and ric, nitric , and acetic acids in an
parts of the eye.
the other hand around the neck or operating fume hood .
• If an acid is splashed onto bare skin,
finger hole. This keeps the bottle closer • During lab, set the acid bottle in a central
rinse with water for at least 15-20
to your body and decreases the risk of dispensing location and have students
minutes.
hitting a sharp object , like a desk bring a graduated cylinder or test tube to
corner, and breaking the bottle. the dispensing area. This will help to • If an acid is splashed onto clothing ,
minimize spills and accidents as well as consider removing the clothing imme-
• Plastic or rubber safety bottle carriers
limiting the amount of acid being trans- diately before the acid soaks through
should be used whenever acids are
ported back to the lab bench. the clothing and reacts with the skin. If
transported from one laboratory to
an acid splashes onto your skin and
another or from the storeroom to a • Instruct students to only remove the
clothing, immediately begin rinSing the
laboratory. amount of acid needed for the experi-
affected skin with water (safety shower
• If a cart is used to transport hazardous ment from the reagent bottle.
is ideal) and then begin to remove
chemicals , such as acids , place Chemicals are never added back to the
affected clothing . Modesty must take a
compatible chemicals inside an reagent bottle.
back seat to the potential chemical ~
unbreakable secondary containment • Have acid spill clean-up materials read- burns that can occur. ...
vessel, such as a plastic tote. The cart ily available whenever acids are used .
• If acid is ingested, the primary goal is
should be equipped with guardrails to • Attach a test tube to the reagent bottle to dilute the acid in the stomach and
prevent plastic totes or bottles from to store the pipets while dispensing prevent further injury caused by
sliding off the cart. acids. vomiting. If the victim is conscious ,
• If hazardous chemicals are moved • Acids are corrosive and will eat through immediately have the victim rinse their
from one floor to another, use an eleva- most fabrics , resulting in small holes in
tor if possible. Only the teacher clothing. Th is process does not occur
transporting the chemicals should be instantly but rather over several hours Always dilute and neutralize
on the elevator. Although elevator acci- and may not become apparent until the acids before disposal.
dents are rare , should a dangerous clothes are washed . Al ways wear a
material be released in an elevator chemical-resistant apron or laboratory
whi le passengers are trapped inside, coat when working with acids. mouth out with water. Have the victim
the results could be catastrophic. drink one or two cups of water or milk.
Personal Protection Gastric antacids such as milk of
Preparation of Acid Solutions Equipment and Safety Aids magnesia or aluminum hydroxide can
See Chemical Solution section , p 953. • Nitrile rubber gloves are acid-resistant also be given . Do not induce vomiting,
To Prepare a Solution and are the best choice to use when do not try to neutralize the acid with a
1. Add the appropriate amount of acid to handling concentrated acids. However, strong base, and do not give the victim
about % of the required amount of any plastic or vinyl glove will provide any sodium bicarbonate or any
distilled or deionized water. some protection against the occasional carbonated drinks. Call a poison
splash, small spill , and splatter that control center or hospital emergency
2. Always add acid to water! Never add occur when using or dispensing acids. room and follow their directions.
water to concentrated acids. The acid
may splatter and generate acidic steam. • Operating eyewashes must be avail - Disposal
able in any classroom or laboratory
3. Always use borosilicate (e.g. , Pyrex®) • Always dilute and neutralize all acids
where acids or acid solutions are used.
glassware. before disposal.
An approved eyewash must treat both
4. Stir to mix the solution . eyes and provide clean potable water • See Flinn suggested laboratory chemi-
for at least 15-20 minutes. cal disposal procedures #24a and #24b
5. Once the solution has cooled to ambi-
in a current Flinn Scientific Catalog/
ent temperature, dilute the solution to • Chemical splash goggles must be
Reference Manual for detailed disposal
the proper volume with water. worn anytime acids or acid solutions
procedures and warninas.
FLI"" ,SCIE"TIFIC I"C. ________"Yc_O_u'_S_a_fe'_S_O_Ufi_Ce_ fl_o'_S_c/_·en_c_e _Su...p...p'_ie_s"
Goggle Safety
equipment so that the protection is
greater than the estimated hazards".
Occupational Safety and Health
What Do the ANSI Standards Really Mean? Administration OSHA 1910.1450
(Laboratory Standard) Section 0(6)
An important obligation of a responsible • There are important factors that are School laboratories should include
science teacher is to provide students difficult to measure and are not "protective apparel compatible with the
with safe, appropriate eye protection. As covered in Z87.1 that must be consid - required degree of protection for
you compare the wide array of goggles ered when choosing eyewear. Among substances being handled".
and safety glasses, you often see the these are durability, comfort, anti-fog
phrase "Meets ANSI Z87.1 Standards" . performance and chemical splash
In the Flinn Scientific CataloglReference protection.
Manual we li st several eyewear styles Keep in mind that not all eyewear is
which all meet th e ANSI stand ard. created equally. There are a lot of
Obviously, there must be more to choos- cheaply-made goggles on the market
ing safe eyewear than merely picking any that will not survive even one semester.
style which meet s this sta ndard. How safe is a goggle if it meets ANSI
To choose the most su itable eyewear standards, but it is left in a desk
for yourself and your students it is help- drawer, unworn, because it is broken or Flinn's most popular
ful to understand ANSI and it s uncomfortable? chemical splash goggle offers
relationship to regulations concerning comfort and coverage.
school laboratories. • Eyewear should fit comfortably and
securely. Try different styles and sizes
What Is ANSI Z87.1? to find the right fit. Basic Recommendations
The American National Standards • Chemical splash goggles should have As you ponder which type of protective
Institute (ANSI) is a non-profit associa- a soft, pliable flange which seals eyewear to purchase , or whether eye
tion which publishes standards covering around the eyes. The hard plastic edge protection is needed at all , keep th e
a broad range of equipment and indus- on models lacking a flange becomes following suggestions in mind:
tries. The complete title of the current extremely uncomfortable. • Will you be using heat, glassware or
ANSI document pertaining to eyewear • The availability of replacement parts chem icals in the lab? If so, it is a good
is American National Standard Pra ctice (headbands, lenses, vent covers) is a basic policy to use protective eyewear.
for Occupational and Face Protection , real cost-saving advantage. • Chemical splash gogg les designed to
ANSI Z87.1-1989. Thi s document provide full coverage around the eyes
• Anti-fog performance is affected
includes standards for several different by temperature and humidity . should be worn whenever hazardous
styles of safety eyewear ranging from
eyeglass-type spectacles to heavy-duty
welding helmets. Each style has its own
standards.
Experiment w ith different eyewear
styles and features (vents and fog-free
lenses) to find the best eye wear for
chemicals are used.
• The educational laboratory is a unique
environment where each student is
III
',
your application. often surrounded by other students
ANSI 's objective is to provide basic conducting experiments. Hazards
performance requirements for eye and Chemical Splash Protection could come from any direction.
face protection. Ju st because eyewear meets Z87.1 Protective eyewear shou ld provide
For example, th e tests listed below are standards does not necessarily mean it sufficient angular coverage .
two of the standards for remova ble provides adequate protection from th e
• Face shields which provide added
goggle lenses: dangers of splashed chemicals. Eye-
splash protection coverage should not
wear that does not provide a complete,
• Lenses shall resist impact from a 25.4 be worn alone. Always wear the appro-
snug seal around the eyes may be fine
mm diameter steel ball dropped from priate goggle or safety glasses
for some activities but not when using
127 cm. underneath a face shield.
hazardous chemicals. When vent open-
• Lenses shall resist penetration from a ings are provided on splash goggles the
projectile weighing 44.2 g dropped Conclusion
vents should be indirect, with covers
from 127 cm. While ANSI has established many stan-
and/or baffles preventing straight-line
dards for a variety of protective eyewear,
For clarification of the relevance of passage of liquids into the goggle.
it does not provide specific standard s
these standards to your choice of labo-
for several factors important to the
ratory eyewear it is helpful to understand The Choice Is Up To You
science teacher. Among those factors
more about ANSI and Z87.1 . As a responsible science teacher, you are durability, comfort , and chemical
• ANSI is not a federal agency. As an must select eyewear which provides you splash protection. It is the teacher's
independent association it is not and your students the most suitable responsibility to keep these factors in
involved in establishing or enforcing protection from the hazards involved in mind when selecting eyewear. As clearly
the OSHA Laboratory Standard. your laboratory activities. The following stated in the Flinn Scientific Catalog/
• ANSI does not test , inspect or approve regulations address the role of the Reference Manual, "You , the instructor,
eyewear. The eye protection manufac- teacher's judgment in selecting suitable should decide what type of eyewear your
turer can choose to contract an eye protection: students must wear in every case. " The
independent testing facility to conduct ANSI ZB7.1 Section 7.3(3) page 15 information and high quality eye and face
tests to determine if their products The teacher must "make a judgement protection Flinn provides will help you
meet ANSI standard s. in selection of the appropriate protective make an informed, responsible choice.
FLlrtrt lCIErtTIFIC IrtC. ________'_'yo_u_r _Sa_fe_r_S_ou_rc_e_fo_r_S_cie_n_ce_ S_u...p-.pl_ie_s"
Overcrowding in the
Science Laboratory
the science classes had enrollments were never designed for the teaching of
teachers considered to be "potentially science. Other teachers have had to
unsafe" for lab work. The average class discontinue the number of hands-on labs
size in these "unsafe" classrooms was they do each year because they now
31 students. Of the 45% of the science have less preparation and set-up time.
classrooms teachers considered to be Overcrowding also increases disci-
"safe," the average class size was 23 pline problems. In a lab situation,
students. One high school teacher discipline problems will result in
surveyed had two classes where the "unsafe" conditions.
number of students was within the
designed enrollment capacity, and three
What is the maximum number of stu- classes where enrollments exceeded the Overcrowding increases
dents you should have in your science room capacity. He said "Contrasting the discipline problems.
laboratory? How much lab space number of accidents between the first
should be available for each science two periods and the last three ... class
student? size does make a significant difference Class sizes in some sc hools have
These are two of the most frequently in traffic flow, individual monitoring, and grown so large that teachers no longer
asked questions we receive each year. understanding of the students!" The run hands-on labs because of unsafe
The frequency of these questions points facts are clear, increasing the number of conditions caused by overcrowding.
out the safety consciousness of today's students in a science laboratory Apparently some teachers have
science teacher. This article is intended increases the likelihood of accidents. A concluded that the risks involved in
to provide you with guidelines on how high pupil/ teacher ratio constitutes a conducting labs in overcrowded labora-
to help solve the problem of overcrowd- threat to laboratory safety. tories are greater than the benefits the
ing in the science laboratory. We hope While we are concerned about the lab experiences provide. How many
you and your administration will evaluate safety of the students, let's not forget science laboratories are considered
and adopt these guidelines in an effort to that overcrowded conditions in the "safe" because the lab work has been
provide a safer working and improved science laboratory also pres ent an removed from the curriculum? Is this the
learning environment for teachers and unsafe working environment for the sci- direction we want science education to
students. ence teacher as an employee of the go? We think not!
Many school districts are experiencing school district. Most science laborato-
budget problems. Any and all solutions ries are designed to accommodate 24 The Professional Standard
to reduce school spending are being students, an accepted professional stan- When discussing the issue of over-
considered. One of the many solutions dard. When class sizes are larger than 24 crowding , teachers and administrators
school administrators are considering to students, it becomes very difficult for the should evaluate not only class size, but
help "ease" budget problems is to science teacher to safely handle, trans- also the amount of space provided each
increase the number of students in each port and use laboratory chemicals and student in the science laboratory.
class . Increasing class size not only equipment. Increased class size puts "at The National Fire Protecti on
delays the need to hire additional teach- risk" the health and safety of the science Association (NFPA) has stated that "50
ing staff, but also postpones the need teacher. sq. ft. net area occupant load factor is
to provide additional classroom space. appropriate for use in science laborato-
For the science laboratory this solution Academic Concerns ries in middle and high schools." For a
creates major problems. Though student safety in the science class size of 24, this would be a 1200 sq .
laboratory is a major reason for limiting ft. laboratory.
class size, another consideration is the The Californ ia Administrative Cod e
Overcrowding increases ability to provide quality laboratory [Title 2 Subchapter 4, Section 1811 (g)]
safety problems. instruction. Many laboratory experiences requires that school design provide 1300
require a high degree of student-teacher square feet for 24 students. This figu re
interaction. The fewer students there are includes preparation areas as well as
Health and Safety Concerns in a laboratory, the greater the opportu- apparatus and chemical storage space.
Sc ience teachers sense that over- nity for students to ask questions and The state of Vermont's revised stan-
crowded conditions in their science for teachers to clarify procedures and dards for approving Vermont 's public
laboratories contribute to lab accidents. encourage the development of reasoning schools (Section 2 160 .4, Page 15 ;
Their safety sense has not failed them! skills. adopted January 2, 1991) states "No
Overcrowding in the science laboratory The amount of personal instruction science laboratory class enrollment shall
is a major contributing factor to the provided each student must be consid- exceed the capacity of the available lab
safety problems school science depart- ered. As one teacher who was teaching stations." This revised standard further
ments face today. in an overcrowded science laboratory states (Section 2191, Page 36, adopted
In 1988, a report published in the put it, "There is simply not enough January 2, 1991) that "classrooms are
Florida Science Teachers Magazine , teacher to go around and give sufficient free of overcrowding and suited to the
Spring Edition, 1988, by Phillip Horton time to each student. " teaching strategies employed ."
entitled "Class Size and Lab Safety in Science teachers report that their
Florida" documented that over 55% of classes are being held in rooms that OVERCROWDING continued on next page.
1-800-452-1261 Class Size
..
as sand, absorbent, neutralizer, and a are ideal for cleaning up mercury spills. and onto the spill. The neutralizer needs to
mercury spill control kit. Small droplets of mercury can also be be mi x ed well with the sand an d
cleaned up by sprinkling zinc dust on the absorbent to come in contact with all of
A 100% wool fire blanket is an excellent the spilled chemical-use a plastic broom
spill control device because it will contain spill area. Zinc dust reacts with mercury to
form a very stable and safe amalgam that to mix well.
and control a spill and its vapors. If a spill
occurs and no spill control materials are is easy to handle, and safe to dispose of in After the spill is controlled , students are
available, simply throw the fire blanket the trash . evacuated and injuries are addressed,
over the spill. The blanket will begin to then the cleanup begins. If the material is
absorb the liquid, contain the vapors, and
Spill Control Procedures warm or still giving off vapors, ventilate
will enable a person to walk over the spill and Training the room and wait before cleaning up. Use
without slipping. Remember, acid spilled A written contingency plan on how to a plastic dustpan and plastic broom to
on a tile floor will become very slippery handle chemical spills should be part of sweep up the now solid mess and place it
and the potential for slipping and falling every school's Chemical Hygiene Plan . into large, heavy-duty garbage or leaf
into the acid spill is a real concern. The following procedure is an example of bags for disposal. If at any time during
a contingency plan. the chemical spill containment or cleanup
Every lab should have spill control step you don 't feel comfortable, leave the
materials that contain at least three 1. Quickly assess the spill , its hazards,
area and get help.
components; sand, an absorbing agent, and the danger to yourself and your
and a neutralizer. Spill control materials students and take appropriate action. If Make spill control containment an d
should be capable of handling a spill from the spilled chemicals are unknown , cleanup part of your annual safety trai n-
the largest bottle used in your laboratory, assume the worst and evacuate. ing. Simulate a chemical spill with water
which is usually a 2 .5-L acid bottle and use sand as the control material. Note
2. Notify other laboratory personnel of the
(remember, Murphy's Law states that the how quickly the "spill" spreads. Practice
accident, and if necessary, evacuate
largest bottle is the one that will break). applying the spill control material around
the area. The safety of you and your
Sand is used to contain a spill, provide and then onto the spill. Determine the
students is always the top priority.
traction , and prevent the spill from rapidly most convenient location for storing your
3. Tend to any injured or contaminated spill control materials. Training is one of
spreading across the tile floor. The
person and if necessary request help. If the most important components of an
absorbent contains and absorbs the liquid
the chemical is splashed into an eye effective safety program .
spill so it is easier to clean up, transport,
or onto skin , immediately irrigate using
and dispose. Neutralizer is usually a base Chemical spills will occur in yo ur
an eyewash or shower. If the chemical
such as sodium carbonate or calcium laboratory. With proper equipment, proce-
is splashed on your clothes, you may
hydroxide and is used to neutralize inor- dures, and training , many spills can be
have time to first contain the spill with
ganic acid spills. If strong bases are used prevented and the spills that do occur can
a fire blanket or spill control materials
in your laboratory, it is wise to keep a be handled safely and effectively.
1-800-452-1261 Laboratory Solution Preparation
Many of the reagents used in science are in the form of solutions ulous procedures are followed . Many of the solutions described
which need to be purchased or prepared . For many purposes, in this section are available ready-made from Flinn Scientific to
the exact value of concentration is not critical; in other cases, save valuable laboratory prep time.
the concentration of the solution and its method of preparation The section is divided into several parts for your convenience.
must be as accurate as possible. The Flinn Laboratory Solution
Preparation reference section is designed for both the novice ~ Basic concepts of preparing solutions
and experienced solution maker. It provides valuable information ~ Preparation of simple inorganic salt solutions
on the basic concepts of preparing solutions and instructions for
~ Preparations of acid and base solutions
preparing most solutions required in the high school science
laboratory. Professional quality solutions are possible when high ~ Recipes for Biological, Histological, and Chemical solutions
quality and fresh chemicals and solvents are used, and metic-
Dissolve 94.16 g of NaCI in about 400 mL of distilled Mass-volume percent solutions are also very common.
water, then add more water until final volume is 800 mL. These solutions are indicated by w/v% and are determined
by the grams of solute per 100 milliliters of solution.
If starting with a solution or liquid reagent:
Example: 1 g of phenolphthalein in 100 mL of 95% ethyl
• When diluting more concentrated solutions, decide what alcohol is a 1 w/v% solution .
volume (VJ and molarity (MJ the final solution should be.
Volume can be expressed in liters or milliliters.
Name I Formula I F.W. Concentration gil Name I Formula I F.W. Concentration gil
Ammonium acetate
Calcium hydroxide saturated 2 gt
1.0 M 77 .1 9
Ca(OH)2
NH 4C2Ha0 2 0.1 M 7.7 9
74.10
77.08
Calcium nitrate 0.5 M 118.1 9
Ammonium sulfate 0.1 M 13.2 9
Ca(NO a)2 • 4Hp 0.1 M 23.6 9
(NH 4)2S04 236.16
132.1
Chromium (III) chloride 0.1 M 26.6 9
Barium chloride 0.1 M 24.4 9
CrCl a • 6HP
BaCI 2 • 2Hp 266.48
244.28
Chromium (III) nitrate 0.1 M 40.0 9
Barium hydroxide 0.1 M 31.5 9 Cr(NOa)a • 9H 20
Ba(OH)2 • 8Hp 400.18
315.50
Cobalt (II) chloride 0.1 M 23.8 9
Barium nitrate 0.5 M 130.7 9 CoCI 2 • 6Hp
Ba(NOal2 0.1 M 26 .1 9 237.95
261 .35
Cobalt (II) nitrate 0.1 M 29. 1 9
Bismuth nitrate 0.1 M 48.5 gin Co(NOala • 6H 20
Bi(NOala • 5H 2O 500 mL6M 291 .05
485.1 HNOa'
Cupric chloride 0.1 M 17.0 9
Bismuth trichloride 0.2 M 63.1 gin CuCI 2 • 2HP 0.5 M 85 .2 9
BiCla 500 mL3M 170.49
315.34 HCI'
Cupric nitrate 0.1 M 24.2 9
CU(NOal2 • 3HP 0.5 M 120.8 9
241 .6
Cupric sulfate 1M 249.7 9
CuS0 4 • 5HP
249.69
Normality: A concentration unit (N); defined as the number
of equivalents of solute per liter of solution . (e.g. , 1 M H2S04 Ferric chloride 0.1 M 27.0 9
= 2 N H2 S0 4) FeCl a • 6H 20
270.32
Saturated Solution: A solution that contains the maxi -
Ferric nitrate 0.1 M 40.4 9
mum amou nt of a particu lar solute that wi ll dissolve at that
temperature. Fe(NOa)a • 9H 20
404.00
Solute: The substance which is dissolved , or has gone into
Ferrous sulfate 0.01 M 2.8 9 and
solution (typically a solid) . 1 mL conc.
FeS0 4 • 7Hp
Solution: A uniform homogeneous mixture of two or more 278.03 H2 SO/
substances. The individual substances may be present in Lead acetate 0.1 M 38 .0 9
varying amounts.
Pb(C2HaO~2 • 3Hp
Solvent: The substance which does the dissolving (typically 379.34
a liquid , such as water or alcohol) . Must be greater than • Add solid to acid solution, stir, then add to water. Dilute to 1 L.
50% of the solution . Remember, always add acid to water.
t Approximate amount for 1 L of saturated solution. Keep adding
Standard Solution: A very precise solution , usually to 3-4 solute until it no longer dissolves; stir for 1 hour, then filter.
Significant figures , used in quantitative analysis or an analyt-
ical procedure.
Supersaturated Solution: A solution that contains more
solute than equilibrium conditions allow; it is unstable and the
solute may precipitate upon slight agitation or addition of a
single crystal. PREPARATION OF SIMPLE INORGANIC SALT SOLUTIONS
continued on next page.
FLI"" .sCIE"TIFIC I"C. ________"Yc_o_u'_S_a_fe'_S_o_u"_ce_"_o'_S_cl_'en_c_e _Su....p...p'_ie_s"
Preparation of Simple Inorganic Salt Solutions, continued
Name I Fonnula I F.W. Concentration giL Name I Fonnula I F.W. Concentration giL
-
t Approximate amount for 1 L of saturated solution. Keep adding
MnCI2 • 4H 2O so/ute until it no longer dissolves; stir for 1 hour, then filter.
197.91
§ Use 7.5 mL cone. HN0 3 to help dissolv.e.
4. Stir until
dissolved.
Add more
water if
2. Fill volu- 3. Transfer necessary.
metric flask SOlid, 5. Add
%-1Jz wash out deionized
full with weighing or distilled
deionized dish. water up
or distilled to mark,
1. Weigh solid.
1-800-452-1261 Preparation of Simple Inorganic Salt Solutions
ID
dibasic Remember, always add acid to water.
K2HP0 4 t Approximate am ount for 1 L of saturated solution. Keep adding
174. 18 solute until it no longer d issolves; stir for 1 hour, then filter.
Name I Rlrmula I F.W. Concentration giL Name I Formula I F.W. Concentration giL
0.1 M 5.6
• Always add acid to water. The addition of acid to water is an
exothermic reaction. Use high temperature (e.g., Pyre ) glassware.
t Extremely exothermic, submerge mixing vessel in an ice bath. See Ice and Water
adjacent box.
*The amount of solute required to prepare one liter of solution.
'tf "\. 171 Concentrated acids are packaged in Flinn Sat-Cubes-" for safe
/ t.iJI shipping and storage.
r:'1 Innovative packaging like the H,O, accordion bottle and the
1.,;.1 E-Z Drop " bottle allow for safe storage and easy dispensing.
1";1 Flinn Chern-Sat " bags, and desiccant packets are standard
a.:.. on many Flinn chemicals.
r:I
Specifically designed MSDS for science teachers included with
~ every chemical.
of Acids Entirely
constructed
of 1" thick,
Flinn/SciMatCo Wooden high denSity,
Acid Cabinets are Ideal 9·ply plywood
and fini shed
for School Storerooms with Super
III
Chem·Tuff"
Corrosive chemicals, such as strong acids Paint.
and bases , must be isolated from other
chemicals to prevent accidental contact and
One fixed·
hazardous reaction conditions. The best way position shelf
to isolate your corrosive chemicals is to store included.
t hem in an approved corrosive storage cabi -
net like the Flinn wooden acid c abinet .
Locked storage cabinets also provide secu-
rity against theft and vandalism.
Interlocking
Flinn wood acid cabinets are designed wooden door
specifically for high school chemical store- assembly.
rooms . Made from nine-ply, high-density
plywood, Flinn acid cabinets are guaranteed
never to rust or corrode.
Flinn acid cabinets will provide long life and a 2" high liquid·tight trough to contain
safe, secure storage for all your corrosives. spillage and provide secondary containment.
See pages 865-868 for more information.
Flinn Acid Cabinets SE8041 Flinn Acid Cabinet; Wood; interior PARTIALLY $591.95"
lined with polypropylene (floor, shelf and
• Wooden acid cabinets are safer and more durable top tray)
than metal cabinets.
SE8051 Flinn Acid Cabinet; Wood; interior COMPLETELY 799.95*
• Acid attacks ALL metal cabinets. lined with polypropylene (floor, interior walls,
interior top and top tray)
• No metal is used anywhere in the interior
construction of Flinn/SciMatCo acid cabinets. * I•• _.~ Cabinet must be shipped by motor truck freight.
1-800-452-1261 Recipes for Laboratory Solutions
Aceto-Carmine (Schneider) See page 79 for a complete Aniline Blue Aqueous Stain
Place 0.5 g of carmine and 55 mL of 01 listing of culture media. 0.5% aqueous: Dissolve 0.5 g aniline
water in a 200-mL flask, bring to a boil, blue in 50 mL 01 water, then dilute to
and add 45 mL of glacial acetic acid. 100 mL. Filter if necessary. (stain for
Alizarin
Plug flask with cotton wool , boil again, algae and fungi)
cool and filter. (stain and fixative, good 0.1 % methanol solution : Dissolve
for protozoa and nuclei) 0.1 g of alizarin in 50 mL of methyl Aniline Blue Indicator
alcohol, then dilute to 100 mL with 0.1 % aqueous: Dissolve 0.1 g aniline
Aceto-Orcein Staining Solution methyl alcohol. (pH indicator) blue in 50 mL 01 water, then dilute to
Heat 31 .5 mL of glacial acetic acid and 100 mL. (pH indicator)
13.5 mL of 01 water almost to boiling . Alizarin Red S
When acid is hot, add 2 g of synthetic 1% aqueous: Dissolve 1 9 of alizarin Baker's Softening Fluid
orcein and allow to cool. Dilute by red S in 50 mL of 01 water, then dilute Mix 10 mL of glycerol, 54 mL of 95 %
adding 55 mL of 01 water; stir and filter. to 100 mL. (pH indicator) ethanol and 35 mL 01 water. (softening
(connective tissue stain) of animal structures)
Alizarin Yellow R
Acetylcholine Bromide Barfoed's Reagent
0.1 % aqueous: Dissolve 0.1 g of
1/ 10,000 solution: Dissolve 0.01 9 of alizarin yellow R in 50 mL of 01 water, Add 10 mL of glacial acetic acid to
acetylcholine bromide in 50 mL of 01 then dilute to 100 mL. (pH indicator) 1 L of 01 water and stir. Add 66.5 g of
water, dilute to 100 mL with 01 water. cupric acetate monohydrate. Heat and
Alum Carmine stir until solid is completely dissolved.
Acridine Orange (test for glucose)
Mix 10 g carmine, 25 g ammoniacal
1% aqueous: dissolve 1 g of acridine alum and 500 mL 01 water. Bring to
orange in 50 mL 01 water, dilute to 100 Benedict's Qualitative Solution
boil , cool , filter and make up to 500 Dissolve 173 g of sodium citrate dihy-
mL, stir and filter if necessary. (biolog- mL with 01 water. (nuclear stain)
ical stain) drate and 100 9 sodium carbonate
anhydrous in 800 mL 01 water. Warm
Aluminon
Adrenaline Hydrochloride and stir to aid dissolution . Filter if
Dissolve 0.1 g of aluminon in 100 mL necessary. In a separate container,
Dissolve 0.1 g of adrenaline hydro-
chloride in 100 mL of Ringer's solution. of 01 water. (qualitative reagent for dissolve 17.3 g copper (II) sulfate
aluminum) pentahydrate in 100 mL 01 water.
Agar (Non-nutrient) Slowly, while stirring constantly, add
Amylase
Suspend 15 g of agar in 1 L of 01 the copper sulfate solution to the first
water. Heat to a boil and stir until 0.5% aqueous: Dissolve 0.5 g of solution. Let cool and dilute to 1 L with
completely dissolved. Let cool to amylase in 50 mL of 01 water, then 01 water. (test for the presence of
50-55 °C and then dispense into dilute to 100 mL. Prepare fresh . (starch simple sugars)
desired containers. Agar will firm as it digestion)
cools. Benedict's Quantitative Solution
Aniline Blue Alcohol Stain Dissolve 18.0 9 of copper (II) sulfate
Agarose Gel 1% alcohol: Dissolve 1 g of aniline blue pentahydrate in 100 mL of 01 water
See page 583 for complete instruc- in 100 mL 85% ethyl alcohol. (stain for and set aside. Dissolve 100.0 g of
tions. cellulose) sodium carbonate anhydrous, 200.0 9
Note: 01 water denotes either distilled or deionized water. RECIPES continued on next page.
of sodium citrate dihydrate, and 125 9 hydroxide in 770 mL of DI water (very commercial formalin (10% formalde-
of potassium thiocyanate in 800 mL DI exothermic; cool vessel in an ice water hyde solution), and 5 mL of glacial
water. Heat, if necessary to aid disso- bath) and cool to room temperature. acetic acid. (plant and animal tissue
lution of the solids. Allow the solution Add all the copper sulfate solution to fixative)
to cool, then transfer to a 1-L volumet- the sodium hydroxide solution.
ric flask. Slowly, while stirring Solution should be blue. (test for Brilliant Blue R-250
constantly, add the copper sulfate proteins) Dissolve 0.25 9 of Comassie brilliant
solution to the 1-L flask. Prepare a 0.1 blue R-250 in 40 mL methyl alcohol.
M potassium ferrocyanide solution by Blood Agar Base Infusion Add 40 mL DI water, then 7 mL
dissolving 0.25 9 of potassium ferro- Suspend 40 9 of blood agar base infu- concentrated acetic acid. Dilute to 100
cyanide trihydrate in 5 mL of DI water. sion in 1 L of DI water. Heat to a boil mL with DI water. (staining proteins in
Add to the 1-L volumetric flask, stir, while stirring vigorously. Boil for one polyacrylamide and agarose gels for
then dilute to 1 L with DI water. Filter if minute. Sterilize for 15 min at electrophoresis)
necessary. (25 mL of this solution is 121 °C (15 Ibs. of pressure) in an auto-
reduced by 50 mg of glucose) clave or pressure cooker. Cool to Brilliant Blue G-250
50-55 °C and pour into sterilized Dissolve 0.1 9 of Comassie brilliant
Bial's Reagent (Sumner) culture dishes. (culture medium) blue G-250 in 25 mL methyl alcohol.
Add 20 drops of 10% iron (III) chloride Add 40 mL DI water, then 5 mL acetic
solution to 100 mL of 95% ethyl alco- Borax Carmine acid. Dilute to 100 mL with DI water.
hol. Add 3 9 of resorcinol and stir. (test Dissolve 2 9 of borax in 50 mL of DI (staining proteins in polyacrylamide
for pentoses and glycuronic acids) water, add 1.5 9 of carmine and boil for and agarose gels for electrophoresis)
30 minutes. Let cool , make up to 50
Bile Salts mL with DI water, then add 50 mL of Brilliant Cresyl Blue
5% aqueous: Dissolve 5 9 of bile salts 70% ethyl alcohol. Let stand for a few Dissolve 0.85 9 sodium chloride in 75
in 50 mL of DI water, dilute to 100 mL. days, then filter. (good general stain for mL of DI water. Add 1 9 brilliant cresyl
Mix gently to avoid foam. plant and animal tissue) blue and stir to dissolve. Dilute to 100
mL with DI water. (vital stain, general
Bismark Brown Y Borax Methylene Blue stain for protozoa and plant cells)
0.5% aqueous : Dissolve 0.5 9 of Heat 100 mL of DI water to 60 °C and
bismark brown Y in 50 mL of DI water, stir in 2 9 methylene blue and 5 9 Brilliant Green
dilute to 100 mL, stir, and filter if neces- borax. Allow to cool slowly. Solution 1% aqueous: Dissolve 1 9 of brilliant
sary. (stain for protozoa) improves with age. (connective tissue green in 50 mL of DI water, dilute to
stain, Negri bodies) 100 mL, stir, and filter if necessary.
Biuret Solution (stain for plant cytoplasm , and pH
Dissolve 2.3 9 of copper (II) sulfate Bouin's Fixative indicator)
pentahydrate in 230 mL of DI water. Mix together 75 mL of saturated aque-
Set aside. Dissolve 308 9 sodium ous picric acid solution , 25 mL of Bristol's Solution
Dissolve 1 9 of potassium dihydrogen
phosphate, 1 g sodium nitrate, 0.3 9 of
magnesium sulfate , 0.1 9 calcium
chloride, 0.1 9 sodium chloride and a
trace of ferric chloride in 1 L of DI
water. (culture of algae)
Prepare Buffer Solutions
See page 101 for a complete list-
Buffer solutions are available from Flinn as premade solutions and ing of indicators and pH ranges.
ready-to-mix capsules and envelopes. Buffers are typically mixtures
of a weak acid and the salt of the acid or a weak base and its salt. Bromcresol Green
This combination is called a conjugate acid-base pair and it will resist 0.1 % alcoholic : Dissolve 0.1 g of
changes in pH upon addition of small amounts of acid or base. bromcresol green in 75 mL of ethyl
Recipes for three common buffer solutions are provided. alcohol , then dilute to 100 mL. (pH
pH 4: Dissolve 5.10 g of potassium hydrogen phthalate in 250 mL indicator)
of DI water, add 0.50 mL of 0.10 M hydrochloric acid, then
dilute to 500 mL. Bromcresol Green
0.04% aqueous: Dissolve 0.04 9 of
pH 7: Prepare 0.10 M potassium phosphate monobasic solution by bromcresol green in 50 mL of DI water,
dissolving 3.40 g in 250 mL DI water. Prepare 0.20 M sodium then dilute to 100 mL. (pH indicator)
hydroxide solution by dissolving 0.8 g in 100 mL DI water. Mix
250 mL of the 0.10 M potassium phosphate solution and 73 Bromcresol Purple
mL of 0.2 M sodium hydroxide solution, then dilute to 500 mL. 0.04% aqueous: Dissolve 0.04 9 of
pH 10: Prepare 0.025 M sodium borate solution by dissolving 2.38 g bromcresol purple in 50 mL of DI
in 250 mL of DI water. Prepare 0.20 M sodium hydroxide water, then dilute to 100 mL. (pH
solution by dissolving 0.8 g in 100 mL DI water. Mix 250 mL indicator)
of the 0.25 M sodium borate solution and 27 mL of the 0.2 M
sodium hydroxide solution, then dilute to 500 mL. Note: 01 water denotes either distilled or
deionized water.
dilute to 100 mL. (pH indicator and Dissolve 0.1 g of neutral red in 60 mL
stain) of 95% ethyl alcohol , then dilute to 100
mL with DI water. Stir and filter if
Methylene Blue, Loeffler's necessary. (pH indicator and vital stain
Dissolve 0.3 g of methylene blue in 30 stock solution)
mL of 95% ethyl alcohol ; add 0.01 g of
potassium hydroxide and 100 mL of Nigrosin
DI water; stir, and filter. (bacterial stain) Saturated: Dissolve 3 g of nigrosin
(water soluble) in 100 mL of DI water.
Methyl Green Stir and filter if necessary. (biological '""""""'....~Slow
1% alcoholic: Dissolve 1 g of methyl stain for protozoa)
green in 75 mL of 95 % ethyl alcohol ,
Microorganisms
then dilute to 100 mL with 95% ethyl Ninhydrin Solutions of methyl cellulose
alcohol. Stir, filter if necessary. Use are commonly used in micros-
Add 2.5 g of ninhydrin to 50 mL of n-
70 % ethyl alcohol if stain is for plant copy to slow the movements
butyl alcohol in a 600-mL beaker.
tissue . (stain for plant tissue and of microorganisms-making
Gently heat and stir the solution using
supravital stain for small organisms) them more readily observable.
a magnetic stirrer/hot plate in a fume
Generally offered as a 2-3%
hood until all the solid is dissolved .
Methyl Orange solution in water, its high vis-
Dilute to 500 mL with n-butyl alcohol.
0.1 % aqueous : Dissolve 0.1 g of cosity physically inhibits the
Use extreme caution when heating n-
methyl orange in 75 mL of DI water, organism. In use, the result-
butyl alcohol, extreme fire risk. (test for
then dilute to 100 mL. (pH indicator) ing dilution will depend on the
proteins)
amount of water present on
Methyl Red the slide when the slowing
4-(p-Nitrophenylazo) Resorcinol
0.1 % alcoholic: Dissolve 0.1 g of agent is added. Some experi-
methyl red in 75 mL 95% ethyl alcohol, Dissolve 0.01 g of 4-(p-nitrophenylazo)
mentation may be required to
then dilute to 100 mL. (pH indicator) resorcinol in 100 mL of 1 M sodium
find the optimal dilution for a
hydroxide solution, stir. (indicator solu-
particular organism. One
Methyl Red tion for magnesium and molybdenum)
technique involves dropping
0.04% aqueous : Dissolve 0.1 g of the methyl cellulose onto a
methyl red in 11 .8 mL of 0.02 M Nutrient Agar
clean slide in the form of a
sodium hydroxide solution; dilute to Mix together 23 g of nutrient agar with ring. A drop of the culture
250 mL with DI water. If using Na salt, 1 L of DI water. Sterilize for 15 minutes being studied is then placed
omit NaOH. (pH indicator) at 121 °C (15 Ibs of pressure) in an into the center of the ring and
autoclave or pressure cooker. Nutrient a cover glass applied. As an
Methyl Violet 2B, Indicator agar should be sterilized if it is being alternative, see the listing for
0.04 % aqueous: Dissolve 0.1 g of used as culture media. Cool to 50- polyvinyl alcohol solution.
methyl violet 28 in 200 mL of DI water, 55 °C and pour into sterilized culture
then dilute to 250 mL. (pH indicator) dishes. (culture medium)
FLI"" lCIE"TIFIC I"C. ________"Yc_o_ur_S_a_fer_S_O_Ufi_Ce_ "_or_S_c/_·en_c_e _Su...p...p'_ie_s"
Recipes for Biological, Histological, and Chemical Solutions, continued
Laboratory
Solutions for Recipes cover biology (culture media and biological
the Science stains), chemistry and physical science solutions used
Classroom in high schools. If you happen to come across a solu-
tion for which a recipe is not included , then the
The Teacher's Handbook explanation section of the book will guide you through
to Solution Preparation the steps of determining the correct procedure for
making the solution.
Need a more complete guide on
solution preparation? Laboratory This reference book is a must for all science teachers!
Solutions for the Science Class- Illustrated, Append ices, Glossary, Index. 1991 , 189
room has been the science teacher's #1 handbook for pages, 5%" x 8%", hard cover.
years. Includes explanat ions of basic concepts and
Catalog No. Description Price/Each
vocabulary terms , detailed recipes of over 300
commonly used solutions, and practical solution- AP8858 Laboratory Solutions for $34.60
making techniques. the Science Classroom
1-800-452-1261 Recipes for Laboratory Solutions
We are sure that responsible science teachers and school When every science teacher or multiple science teachers are in
administrators agree that it is necessary to know exactly what charge of th is matter-then, in fact, no one is in charge.
chemical substances are present on school premises and in Multiple school building districts should also give very serious
what quantities. Such an inventory would serve many valuable consideration to establishing a central "filter committee." This
purposes such as (but not limited to): committee could routinely see every chemical requisition . Their
• To comply with regulatory requirements review would be aimed at completely eliminating or reducing the
• To make the school safer quantity of so me substances purchased . No, we are not
suggesting that science teachers be denied access to needed
• To efficiently use (and perhaps share) the existing inventory
reagents. We are, however, suggesting that the matter be well
• To rid the premises of excess/unused chemical substances managed. Who better to manage the problem than the knowl-
• To implement the storage of all remain ing substances in edgeable users; i.e., the sc ience teachers meeting as a
compatible chem ical famil ies comm ittee.
• To isolate and safely store particularly hazardous substances It is not uncommon to find, among mu ltiple school bui ldings,
an excess of a chemical in Building A while the science teacher
• To create and maintain a perpetual inventory of all chemical
in Building B just placed an order for the very same chemical.
substances
Why can 't inventories be shared with the goal in mind of better
• To identify substances (severe toxins, carcinogens, etc.) that
should not be found on school premises and rid the premises
of these materials
• To identify substances as a function of their specific hazardous
character (flammables , acids, oxidizers, etc .) and provide
dedicated and approved storage for them .
In our opinion , just plain old-fashioned "good sense" suggests
that it is time for action! Action demands that you know what
you have and how much of it you have. Once this inventory is
accomplished a great many benefits will follow.
It is very important to point out that laboratory chemicals
should no longer be purchased like other routine school
supplies! The normal routine of most schools is to acquire a
year's supply of needed chemicals at one time, along with other
routine science supply needs. The result of this process is that
dozens of chemical items, many in very large quantities, arrive
at the school and are then stored in science storerooms never
designed to handle such quantities and rarely equipped to meet
even minimum standards of safe storage. We are sure your
conventional wisdom says that the smaller the quantities of
these materials found in schools at any given time, the smaller
the problem .
We cannot emphasize strongly enough the need for science systemwide substance management? If the impediment to
teachers, science department heads and , most particularly, better, safer and more efficient substance management is the
school administrators and business managers to recognize the "establ ished system" or the "established bureaucracy" then
problems created by lumping hazardous chemicals into the the "system" or the "bureaucracy" must be educated and their
buying routine. To continue to apply the same buying routine to methods changed. Would you not agree that an efficient method
hazards simply aggravates and perpetuates the problem. Those of substance management in a multiple science department
in the school with science backgrounds must educate the non- building or in multiple buildings is to provide inventory level
science-trained administrators about the severe probl ems information to all users and allow all users access to excess
created by continuing to buy hazardous chemicals in the same inventories? No, one school should not be allowed to rob
manner as they buy routine school suppl ies. another school 's inventory. However, can 't excesses be identi-
It can also accurately be stated that when a large school fied and shared? The science teacher who is a good substance
with many science teachers has no one in charge of managing or inventory manager shou ld not be penalized to serve the poor
the chemical storeroom , the problem is made more severe. Continued on next page.
1-800-452-1261 Chemical Inventory
manager in another departm ent or buil ding . Conventional a microphone that wou ld hang around your neck or be attached
wisdom suggests, however, that excess su bstances can be to your co llar. This would free both hands so you can have
better managed by sharing knowledge of their existence. maximu m flexibility in moving about the storeroom.
You have now decided it is time to take an inventory. Plan for It is an absolute that you never undertake an inven tory
the event using the Inventory Planning Checklist below. alone. You must always have a teammate. The teammate is
A very effective means of takin g and temporarily recording there to help you, to hold a ladder, to go for help or just to be
your inventory is by means of portable dictation equipment. there but, in any case, you should never work alone. We urge
Perhaps you can fin d, at the schoo l or at home , a battery- against recruiting students. It is also an absolute that the right
operated recording device. It would be ideal if the device could kind and type of fire extinguishers be in the room with you and
be placed in your pocket or attached to your person along with immediately avai lable for use.
Continued on next page.
• Who will be the team members to perform the • Have you undertaken and completed as much
inventory? storeroom housekeeping as possible prior to the
inventory so you are not faced with obstacles that
• How much time shall you allow to perform this task? would lead to an accident?
• As materials are taken from the shelf (if you elect • Have school authorities and maintenance people
to do this at this time) where and how will they then been alerted to this inventory undertaking?
be housed?
• If you elect to do some disposal during the inventory
• Do you have the requisite safety items to protect process (we urge against this) are the reacting
yourselves during the process? chemicals available?
• Will this be simply an inventory of what substances • Have you arranged for the process to be free of
you have or will it be a major reorganization of the interruptions that might distract you at a critical
chemical stores facility? moment?
• Are flashlights, ladders and other such devices • Will the team members performing the inventory be
available? wearing appropriate clothing?
• Will the room be properly ventilated during the • Will all sources of ignition be eliminated?
process?
• Is it your plan to add some form of label or other
• Will a means of communicating with the outside kind of identification to each chemical container and,
be available in case of a serious problem like spill , if so, have you decided how this is to be done and
breakage or fire. are the means to do it available?
• How will you record the chemicals on a substance- • Will you have a supply of replacement caps available
by-substance basis? for containers with bad closures? If you expect to
transfer some substances to alternate containers-
• How will you handle unknowns or "mystery"
are such available?
substances as these are encountered?
• What will be done with the many bottles of solutions
• Will spill materials, such as sand, neutralizers, etc.,
that have been prepared and stored for lab use over
be available and, if yes, which have you chosen?
the past years? Will you include these in your inven-
• Will alternate containers (empty bottles, cans, bags, tory? How?
etc.) be available when a broken container is
• If you expect to rearrange your chemical shelves
encountered? during the process are shelf labels available?
• Is there a plastic broom, plastic dust pan and plastic • Do you expect to identify substances by their
receptacle available for cleanup? hazardous character during the process? If yes, will
• Have you made arrangements for the removal of you then house them (like flammables, acids, etc.) in
unwanted substances or, if you want to isolate these dedicated and approved cabinets? Are the cabinets
materials, have you planned for temporary and safe now available? Is there sufficient space in the exist-
storage methods while you examine your disposal ing cabinets?
options? • Will the method you select t o record this inventory
• Will a fume hood be available to very temporarily allow you, if you elect to do so, to perpetually main-
store a substance which, upon discovery, needs tain the inventory?
your immediate attention? • Will you have tape or an adhesive of some kind
available to affix loose labels? Will you have blank
labels available to place on currently unlabeled
materials which you can identify with accuracy?
FLI"" lCIE"TIFIC I"C. ________"Yc_O_u'_S_afl_e'_S_o_u"_ce_ fl_o '_S_cl_·en_c_e _Su..,;"p...p'_ie_s"
CHEMICAL INVENTORY continued Your next step is to transcribe this information into hard copy.
Another absolute is that you are appropriately dressed and That copy may take the form of 3" x 5" cards, sheets of paper,
spill materials are present. In general, we assume you have done etc. You may even w ish to consider acquiring the Flin n
all the preplanning and all the plans have been implemented. computer chem ical inventory system (see page 904).
With your recording equipment operable you now start across Next assign compatible chemical family designations and
your shelves. You recite into the recording equipment the full hazard data to each listing. Our computer chemical inventory
name of each substance, the approximate size of the container system has established 15 alpha designations to identify
and the amount of the contents. A typical recording might sound hazards. You may wish to use this same system to code your
like, "One 5-lb. bottle, glass container, of acacia, about one-half list. The designations are shown below.
fu ll. " If you wish , you might want to spell the name of each
substance. Some schools turn this tape over to their business
training department for typing . If a non-technical person would,
at some later time, be called upon to transcribe this data you
Flinn Hazard Caution Codes
must be articulate and spell the name of each substance. Such A Flammable
detail only takes a matter of seconds on your dictating tape. B Volatile
C Toxic
D Strong oxidizer or reducer
One kilogram E Carcinogenic
plastic bottle of
F Produces Peroxides
sodium carbonate
monohydrate .. . G Skin and/or eye irritant
about half full. H Contains harmful impurities
Unpredictable explosive
J Harmful dust or vapors
K- Avoid contact with water
l- Avoid contact with air
M- Corrosive
N Allergen
0- Avoid contact with organic material
-
or transfer as possible. shelf first. No, do not simply acquire some cartons and pile
It is unlikely that you will want to reorganize your shelves at this bottle upon bottle into cartons and create a new problem.
time since your primary goal is to determine what you have Rather, use your conventional wisdom and ask yourself if the
and how much of it you have. Once the inventory is complete item is hazardous and then investigate its hazardous character.
and has been converted to hard copy then you can begin to
think about the reorganization process. At this point focus on
just discovering and recording what and how much you have. Be able to call for help in the
You really should not consider major reorganization until you event help is needed.
know the "what and how much" since these facts may cause
you to elect not to set shelf space aside for substances you wish
to eliminate from your inventory. It is our experience that in an Should it be physically isolated? An example please. Let's
average school (if there is such a thing as an average school) assume you find a 500-gram bottle of aluminum chloride, anhy-
four out of ten bottles on the shelves have not been used in the drous, and you wish to rid yourself of this substance. You do not
last five years and will not be used in the next five years. There know how to achieve this but you want it off the shelf and yet
is no need to dedicate shelf space to such excess substances. protected and safe for later disposition. Place the bottle in three
If your shelves and cabinets are just loaded and a lot of move- thicknesses of Baggies®. You can get Baggies at you r local
ment of substances is required to inventory all the materials, grocery store. Flinn has heavy duty plastic bags called Chem-
then the task will require several hours. If however, most Saf® Bags for this purpose. You will find Chem-Saf® Bags listed
substances can be viewed and recorded with little bottle shift- on page 887 in this Catalog/ Reference Manual. Next, acquire
ing or relocation then even a very large high school chemical some clean , never-used, one-quart and one-gallon paint cans.
stores facility will not require much more than about 2-2112 hours Flinn has such containers called Saf-Stor® Cans. These are also
to record all of these substances on your tape. The use of a listed on page 887 in this Catalog/ Reference Manual. You can
portable, battery-operated, necklace microphone recording acquire similar cans (less heavy duty) at a local paint store or
instrument is a very efficient means of rapidly concluding this store that might sell and mix paints to order.
part of the process. Continued on next page.
1-800-452-1261 Chemical Inventory
Now, line the bottom of the can with just enough vermiculite The cans will serve to protect against breakage and even act
or cat litter (cat litter is bentonite) to cushion the plastic bag- as a miniature fire cabinet to prevent these hazards from being
enclosed bottle. Place the plastic bag-enclosed bottle in the directly involved in a conflagration.
center of the can. Fill the remaining empty void of the can with Those substances which remain on your shelves can now be
vermiculite or cat litter. Place the fri ction lid on the can and reorganized into their compatible chemical families. We urge that
label the outside of the can with the chemical formula of the you review all the details of appropriate and safe storage in the
substance contained therein. By using the chemical formula section of this Catalog/Reference Manual dedicated to that
rather than the full name you can th wart the potential vandal subject.
intent upon securing or using a hazardous chemical. The vandal
simply will not be able to read the formula. Avoid distractions.
You have now provided a secure container for this unwanted
substance. You may now assign an area in the storeroom where For the first time you know exactly the substances and their
such hazards will be safe until you investigate and ultimately quantities in your chemical stores area. It is from this base of
exercise your disposal or removal options. You will find that knowledge that you can begin to manage this matter of chem-
plastic bags and cans can be among your best friends for isolat- icals on school premises. You needed to take this first, important
ing and containing hazards during your investigation. step. You may need further help and advice. If you do, call Flinn.
Reorganize the remaining products into their compatible chemical families (see our Suggested Chemical Storage
Pattern on page 967). The actual sequence of compatible families on your shelves is not critical. What is important is to
keep the compatible families separate and to keep the organic and inorganic families as far apart as possible. The
Suggested Shelf Storage Pattern shown on pages 968-969 is only one suggested sequence you can use. If shelf space
is a problem , you are permitted to place more than one compatible family on a shelf. Make sure you either have a phys-
ical divider or leave a 3" space between each family.
Hundreds of teachers who have reorganized their shelves, using these patterns, tell us products are easier to find versus
the alphabetical system previously used. When you reorganize, you may need some estimate of the percentage of shelf
space each family might occupy. If yours is a "typical " high school, the following profile may be a helpful guide:
Inorganic Families
Families Percentage of Shelf Space Occupied Families Percentage of Shelf Space Occupied
Acids Store away from all other items. Store Sulfides, etc. Less than 1 %
(I norganic 9) in a dedicated acid cabinet. Store nitric (Inorganic 5)
acid away from all other materials.
Chlorates, 5+%
Metals, etc. Less than 5% Perchlorates, etc.
(Inorganic 1) (Inorganic 6)
Halides, Sulfates, Could be 35-40% of available space.
Arsenates, etc. Less than 1 %
Phosphates, This is usually the largest family.
(Inorganic 7)
Acetates, etc.
(Inorganic 2) Borates, Less than 1 %
Nitrates, etc. Approximately 8-10 % Chromates, etc.
(Inorganic 3) (Inorganic 8)
Congratulations! You have now reorganized your chemical stores facility to:
• store compatible products together • lock up all poisons
• separate acids into dedicated storage • record all inventory
• separate flammables into dedicated storage • rid yourselves of excess materials
Inorganic Organic
1. Metals, Hydrides 1. Acids, Amino Acids, Anhydrides, Peracids
2. Acetates, Halides, Iodides, Sulfates, Sulfites, 2. Alcohols, Glycols, Sugars, Amines, Amides, Imines,
Thiosulfates, Phosphates, Halogens Imides
3. Amides, Nitrates (except Ammonium Nitrate), Nitrites, 3. Hydrocarbons, Esters, Aldehydes, Oils
Azides
4. Ethers, Ketones, Ketenes, Halogenated Hydrocarbons,
4. Hydroxides, Oxides, Silicates, Carbonates, Carbon Ethylene Oxide
5. Sulfides, Selenides, Phosphides, Carbides, Nitrides 5. Epoxy Compounds, Isocyanates
6. Chlorates, Bromates, Iodates, Chlorites, Hypochlorites, 6. Peroxides, Hydroperoxides, Azides
Perchlorates, Perchloric Acid, Peroxides, Hydrogen
7. Sulfides, Polysulfides, Sulfoxides, Nitriles
Peroxide
8. Phenols, Cresols
7. Arsenates, Cyanides, Cyanates
9. Dyes, Stains, Indicators
8. Borates, Chromates, Manganates, Permanganates
10. Organic miscellaneous
9. Acids (except Nitric) (Nitric Acid is isolated and stored
by itself.)
10. Sulfur, Phosphorus, Arsenic, Phosphorus Pentoxide
11. Inorganic miscellaneous
NOTE: If you store volatile materials (ether, hydrocarbons, etc.) in a refrigerator, the
refrigerator must be explosion-proof. The thermostat switch or light switch
in a standard refrigerator may spark and set off the volatile fumes inside
and thus cause an explosion.
Surely this list is not complete and is intended only to cover the materials possibly found in an average school
situation. This is not the only method of arranging these materials and is only offered as a suggestion.
See the next three pages for detailed inventory and storage steps you might follow to
vastly improve the safety profile of your chemical storage.
FLlrtrt SCIErtTIFIC IrtC. ________"Yi_o_ur_S_afl_er_S_o_u"_ce_ fl_or_S_cl_oen_c_e _Su_p...p'_ie_s"
SUGGESTED SHELF STORAGE PATTERN-INORGANIC
INORGANIC #2 INORGANIC #5
Halides, Sulfates, Su lfites, Thiosulfates , Sulfides, Selen ides, Phosphid es,
Phosphates, Halogens, Acetates Carbides , Nitrides
INORGANIC #3
Amides , Nitrates (not Ammonium Nitrate) , INORGANIC #8
Nitrites, Azides Borates, Chromates, Manganates,
(Store Ammonium Nitrate away from Permanganates
all other substances-ISOLATE IT!)
INORGANIC #1 INORGANIC #6
Metals & Hydrides Chlorates, Bromates, Iodates, Chlorites,
Hypochlorites, Perchlorates,
(Store away from any water.)
Perchloric Acid , Peroxides,
(Store flammable solids in flammables cabinet.)
Hydrogen Peroxide
INORGANIC #4
Hydroxides, Oxides, Silicates, MISCELLANEOUS
Carbonates, Carbon
If possible
avoid
using the
J l floor.
J
....
~ Storage Suggestions
1. Avoid floor chemical storage (even temporary).
2. No top shelf chemical storage.
3. No chemicals stored above eye level. INORGANIC #9
4. Shelf assemblies are fi rmly secured to walls. Avoid island
shelf assemblies. Acids, except Nitric
5. Provide anti-roll-off lips on all shelves.
(Acids are best stored in
6. Ideally, shelving assemblies would be of wood construction. dedicated cabinets.)
ORGANIC #2
Alcohols , Glycols, Sugars, Amines , ORGANIC #8
Amides , Imines, Imides Phenols, Cresols
(Store flammables in a dedicated cabinet.)
;,
ORGANIC #3
ORGANIC #6
Hyd rocarbons , Oil s, Esters , Aldehydes
Peroxides, Azides, Hydroperoxi des
(Store flammables in a dedicated cabinet.)
<-
ORGANIC #4 ORGANIC #1
Ethers, Ketones, Ketenes,
Acids, Amino Acids ,
Halogenated Hydrocarbons,
Anhydrides, Peracid s
Ethylene Oxide
(Store certain organic acids in acid cabinet.)
(Store flammables in a dedicated cabinet.)
, ,
ORGANIC #9
ORGANIC #5
Dyes, Stains, Indicators
Epoxy Compounds, Isocyanates
(Store alcohol-based solutions in flammables cabinet.)
ORGANIC #7
MISCELLANEOUS
Sulfides, Polysulfides, etc.
If possible
avoid
.. using the
J L floor.
J l
ORGANIC #2
Alcohol s, Glycols, etc.
Maximize
ORGANIC #3 Storage Space
Hydrocarbons, etc. Store
If shelf space is a problem,
severe you are permitted to place
ORGANIC #4 more than one compatible
Ethers, Ketones, etc. poisons in chemical family on a shelf.
locked Make sure you either have
ORGANIC #9 a physical divider or leave a
Alcoho l-based Indicators, etc. Poisons 3" space between each
family. Th is will maximize
Cabinet.
your tight shelf space while
keeping each compatible
chemical family separate
from one another.
See page 966 for complete instructions on organizing your chemical stores area.
FLI"" lCI E"TIFIC I"C. ________"Yc_o_ur_ S...a _fer_ S;.;,o..;;.,u"..;;.,ce,;",,;f.Ior
;,;..,;;S;.;.,
cl;·en
.;,;.;,;;c.;.,
e .;,;
Su;;;,:;;
p;,:;;
pl;;.;;;
ie,;..s"
I:]
All chemical products arranged Posted school safety policy
on shelves in chemically- (student contract).
compatible families. Some
categories of products
~
(flammables, corrosives, etc.) Eyewash/face drench station
isolated from all other products in plumbed into potable water
their own dedicated cabinets. supply. Portable or squeeze
bottle eyewashes not
Shelves equipped with "anti- - -+--+-- - ----e considered satisfactory!
roll-off lips" to prevent tipped
containers from cascading to Chemical First Aid Kit.
the floor. Telephone available for emergency use - - -... 1
with emergency numbers posted alongside.
25-pound pail of dry sand for Wall-mounted, woolen fire
Interior walls should be of
spill containment/absorption. - -- - -•• blanket
continuous floor to ceiling
masonry construction . A false 25-pound pail of neutralizer chemical _ _ _ _
for hazardous liquid spills. e Secure door lock (dead bolt
ceiling may enable fire or toxic variety). Student access not
fumes to easily flow to other allowed .
portions of the building . Inexpensive, automatic, Door(s) to stores area (as well
ceiling-suspended fire as individual cabinet doors)
extinguisher(s). should be placarded (labeled)
Solid core door
Insist that your chemicals - - -+-+-. to identify hazardous contents.
This is done to alert and
(preferably no glass
(wherever possible) be windows). Ideally,
supplied in plastic or metal protect firefighters.
the room should
containers rather than less have two doors.
safe glass. Store no chemicals on the floor. Floor covering
should be of least reactive materials.
Self-closing door return to
Compressed gas cylinders -------1I-+- - - - - - - h
ensure containment of fire
firmly chained to wall in an
upright position. or fumes.
At least two (2) Type ABC,
Ventilation system isolated ---l'--+----~ 15-pound, portable , wall-mounted
fire extinguishers. One located at
from rest of building; room
the far interior of the stores area;
temperature well below 25 °C;
the second located near the door.
room air changed four times
per hour.
Supply of spill containment/
absorbent materials available for
Outside Wall emergency. Spill treatment kits
not considered satisfactory.
..
If all of these options prove fruitless, you are left with two options: Y'"J";:~;;;;;~~ HAZARDOUS
,.......~-...r-J\
Disposal Procedures
FLINN METHOD o
# 1a ORGANIC ACID HALIDES AND
Place the saturated solution of sodium carbon-
ate in the large glass or plastic container.
ACID ANHYDRIDES
Products in this class readily react with water, amines, and alcohols.
They should never be allowed to come into contact with wastes that Acid
contain such substances. They are also generally corrosive and Halide
their vapors are lachrymators. Most organic acid halides can be
decomposed to water-soluble products of low toxicity that can be
flushed down the drain. Heat may be liberated during this process.
The heat can be controlled by immersing the reaction vessel in a
larger container of ice water.
EXAMPLES:
Acetyl chloride, adipoyl chloride, and acetic anhydride
MATERIALS REQUIRED:
Chemical-resistant gloves
Chemical-resistant apron
o
Slowly add a few milliliters or grams of the acid halide or anhydride
Chemical splash goggles or full-face shield to the container while constantly stirring. You can tell that the
Fume hood or excellent ventilation decomposition reaction is beginning if the material dissolves. The
Large glass or polyethylene container evolution of gaseous carbon dioxide should also be evident.
Saturated solution of sodium carbonate (200 g NaCO:lL),
enough for twofold molar excess
Stirring rod
3 M hydrochloric acid
pH indicator paper
Ice-water bath (optional)
o
If a noticeable temperature rise is
observed in the solution, place the con-
CHEMICAL CONCEPT: tainer in the optional ice-water bath .
Organic acid halides are derived from organic acids by replacing the This may occur with acetic anhydride.
ionizable hydrogen atom of the acid with a halogen atom, usually I lb ::::ill \
~
chlorine. These substances react with water to form the original
organic acid and hydrogen chloride, both of which will usually Ice and Water
dissolve in excess water and form an acidic solution. This is the
reason these compounds are corrosive and are lachrymators: their
vapors react with the tears (mostly water) that bathe your eye and
make them acidic. The disposal method involves two simultaneous
steps . The saturated sodium carbonate solution contains both
water and a base, sodium carbonate. The organic acid anhydride or
halide reacts with the water, and the products of that reaction,
which are acidic , immediately react with the sodium carbonate to
form salts of the acids. These salts are innocuous and may be
flushed down the drain. Gaseous carbon dioxide also forms, which
o
Continue slow addition of
will produce a fizzing as the reaction proceeds. the acid halide while stirring
In the case of acetyl chloride, the reactions are as follows : until all the compound has
been consumed .
CH 3 COCI + H2 0 -7 CH 3 COOH + HCI
CH 3COOH + %Na2C0 3 -7 NaCH 300 + %C0 2 + %H20
HCI + %Na2C03 -7 NaCI + %C0 2 + %H2 0 FLINN METHOD #1a continued on next page.
o
When a clear solution has been obtained, cool it to room tempera- 0
ture and neutralize it to pH 7 with the 3 M hydrochloric acid.
Prepare an ice/water slush in a large glass or polyethylene container.
Slowly add the water-reactive metal halide directly to the ice/water
slush with constant stirring. Aluminum chloride reacts vigorously
with water. Be cautious to avoid localized overheating.
o
Flush the neutral mixture down the drain with a 20-fold excess
of water.
.,
When all the compound has been added to the water, allow the
mixture to come to room temperature and neutralize to pH 7 with
FLINN METHOD sodium hydroxide or sodium carbonate solution. If you use sodium
carbonate solution, expect some evolution of carbon dioxide gas
# 1b WATER-REACTIVE METAL HALIDES during neutralization. A thick white precipitate of aluminum or stan-
nic oxide will form.
Products in this class are quite reactive with water and evolve heat
during the reaction. Such reaction products are strongly acidic.
Water reactive metal halides must not be allowed to come into
contact with wastes containing water. They can generally be
decomposed to products suitable for flushing down the drain by
reacting them with a large excess of cold water and neutralizing the
resulting acidic solution.
EXAMPLES:
Aluminum chloride (anhydrous) and stannic chloride
MATERIALS REQUIRED:
Chemical-resistant gloves
Chemical-resistant apron
Chemical splash goggles or full-face shield
Fume hood or excellent ventilation
Large glass or polyethylene container, % filled with ice/ water slush
Stirring rod
3 M sodium hydroxide solution or Let the mixture settle overnight and then decant the liquid to the
saturated sodium carbonate solution drain with a 20-fold excess of water. The solid residue can be
pH indicator paper disposed of in the trash .
CHEMICAL CONCEPT:
As described above, these substances react with water, and the
products are acidic. For example:
SnCI 4 + 2H 20 --7 4HCI + Sn02
The HCI formed will dissolve in the excess water. It is neutralized
with either sodium hydroxide (to form sodium chloride and water) or
with sodium carbonate (to form sodium chloride, gaseous carbon
dioxide and water).
1-800-452-1261 Chemical Disposal Procedures
PROCEDURE B:
FLINN METHOD
#2 ALDEHYDES
Products in th is class may be solids, liquids, gases or aqueous
solutions. We recommend simple evaporation for small amounts of
low- boiling liquids and th eir aq ueous solutions. Higher- boiling
liquids and solids are flammable and incinerati on is a good option .
Many jurisdictions will permit formaldehyde and acetaldehyde to be
drain-d isposed . Check with local authorities before proceeding to
dispose of formaldehyde, formal in and acetaldehyde down the
drain .
EXAMPLES:
Acetaldehyde and benzaldehyde
MATERIALS REQUIRED:
Th is procedure must be performed in a fume
Chemical-resistant gloves
hood. A mixture of 100 mL of water and 0.2
Chemical-res istant apron
moles of aldehyde is stirred in a 1-L beaker.
Chemical splash goggles or full -face shield
Fume hood or outdoor site for evaporati on
Large metal pan (for evaporation only)
1-L beaker
Th ermometer
pH indicator paper
Magnetic stirrer/ hot plate and stir bar
8:00 O'Clock
0.3 M potassium permanganate, KMn04, 500 mL
0.1 M sodium sulfite, Na2S03
3 M sulfuric acid
CHEMICAL CONCEPT:
Aldehydes are organic compounds that contain a carbonyl group
bonded to at least one hydrogen . Their carbonyl group is easily
oxidized to a carboxylic acid , which is usual ly less toxic , less
volatile, and more water soluble than the starting aldehydes.
The oxidation is performed using aqueous potassium perman-
ganate. Potassium permanganate is a stro ng oxidizing agent and
the reaction can be followed by monitoring the color change. As the
oxidation occurs, the purple permanganate (M n0 4-) is reduced to Add about 30 mL of 0.3 M potassium permanganate solution over
a brown manganate dioxide resulting in a loss of purp le color. a period of 10 minutes. If this addition is not accompanied by a rise
For example: in temperature and loss of purple permanganate color, then heat the
3C 6 H5CHO + 2KMn04 ---7 mi xture using a hot plat e until a temperature is reac hed that
2C6 H5C02K + C6 H5C02H + 2Mn0 2 + H20 changes the color.
The reaction can be performed in a 1-liter beaker in a hood . The
reaction also needs to be heated after th e potassiu m perman-
ganate has been added. Lastly, any excess permanganate must be
red uced by sodium sulfite before final disposal of the soluti on . For
glutaraldehyde which contains two aldehyde groups, twice as much
permanganate is requ ired.
9:00 O'Clock
PROCEDURE A:
~£
,-
Sodium ........
~
FLINN METHOD
#3 ALKALI METALS AND ALKALINE
Place several pieces (10-20 g) of freshly cut
EARTH METALS metal in a 500-mL beaker. Make sure the metal
is covered with a little mineral oil. Use a mag-
Materials in this class may be reactive with air and with liquids
netic stirrer or stir rod to stir the mixture.
such as water, alcohol, and halogenated hydrocarbons. They should
not be allowed to come into contact with wastes containing these
liquids. The alkali metals are usually stored in a liquid hydrocarbon
to keep them from air. The alkaline earth metals are usually covered
with a thin coat of metal oxide which protects them from further
oxidation. The best way to dispose of alkali metals is reaction with Slowly add ethyl
an alcohol (procedure A) while alkaline metals can be reacted with alcohol (at least 13
water or dilute acid (procedure B). All the metals are also destroyed mL per g sodium ,
by incineration (see Flinn Disposal Method #26c) . 30 mL per g lithium)
to the metal at a
EXAMPLES: rate to cause a rea-
Alkali metals include lithium, sodium and potassium. Alkaline earth sonable hydrogen
metals include magnesium and calcium. evolution. Do not
MATERIALS REQUIRED: add the ethyl alcohol too
Chemical-resistant gloves fast (causing excessive heat
Chemical-resistant apron generation). Stir the reaction
Chemical splash goggles or full-face shield mixture until all the pieces of
Fume hood metal have dissolved.
Class 0 fire extinguisher or a large bucket of clean , dry sand
Large glass beaker
Magnetic stirrer and stir bar; or stir rod
Knife to cut large pieces of metal (optional)
pH indicator paper Only after all pieces
Ethyl alcohol, anhydrous (for sodium and lithium) of metal are gone,
tert-Butyl alcohol (for potassium) slowly add an equal
1 M hydrochloric acid volume of water to
the reaction mi x-
CHEMICAL CONCEPT:
ture. Neutralize with 1M
Alkali metals are very reactive with water to produce a base (e.g., 1 M hydrochloric
NaOH), hydrogen gas, and heat. They also react with alcohols in a Hel
acid .
more controlled manner to give similar products. The reaction is
slower in alcohol due to the lower acid dissociation constant of No metals left ,n
alcohol relative to water.
Na + CH 3CH 20H --'» CH 3 CH 20 Na + 'l2H2 FLINN METHOD #3 continued on next page.
1-800-452-1261 Chemical Disposal Procedures
PROCEDURE:
oro n o
Immerse the plastic-capped container upside-down in the beaker
of water. Allow it to stand for four hours to permit water to work its
way up the threads between the cap and the bottle.
4:00 O'Clock
o
Without touching your container of picric acid, determine if it has a
metal cap. If it does, do not touch the container at all.
Remove the bottle from the beaker. Uncap it. Fill the bottle with
water and replace the cap.
Picric
o
A metal-capped container of picric acid should be handled only by o
4:05 O'Clock Acid
a trained expert such as a member of a bomb squad . Call such an Re-invert the bottle. Allow it to stand
expert to remove the material from school premises as soon as for several days to thoroughly wet all
possible. (Picric acid can form salts with the metal in the cap and the material inside.
these salts are more explosive than picric acid itself. The friction
caused in attempting to remove the metal cap from a container of
picric acid has been reported to cause detonation of minute
amounts of metal picrate trapped in the threads of the cap.) FLINN METHOD #4a continued on next page.
1-800-452-1261 Chemical Disposal Procedures
-=
o
Call a commercial waste disposal service, the local bomb squad , or
PROCEDURE:
fire department and have them remove the material from school
premises .
8:00 O'Clock
Amine
FLINN METHOD
#4b HALOGENATED HYDROCARBONS
Halogenated hydrocarbons where the halogen is attached directly
to an aromatic ring (e .g., benzene) or carbon-carbon double bond
are difficult to destroy by chemical means. Halogenated hydrocar-
bons that contain no carbon-carbon double bonds or have low
o
This procedure should be performed in a fume
boiling points can be destroyed using Flinn Disposal Method #27j . hood. Dissolve 5 mL of the aromatic amine in
The best route for disposal of nonvolatile halogenated hydrocarbons 250 mL of 3 M sulfuric acid in a 1-L beaker.
is through incineration. Use either a commercial waste disposal
service or Flinn Disposal Method #26c.
Potassium
EXAMPLES:
Permanganate
Bromobenzene, dichlorobenzene, and perchloroethylene ;
10:00 O'Clock
FLINN METHOD
#4c ORGANIC ACIDS, SUBSTITUTED oSlowly add 50 g of potassium
Substituted organic acids include amino acids and halogenated permanganate to the acid/amine
carboxylic acid (e.g. , chloroacetic acid). Amino acids are water mixture over 2 hours. Stir the
soluble and usually have nutritive value. Amino acids are easily mixture at room temperature for
disposed of using Flinn Disposal Method #26a or #26b . Most water two days (48 hours).
soluble substituted carboxylic acids and their sodium , potassium,
calcium or magnesium salts can be washed down the drain if local
regulations permit. See Flinn Disposal Method #26b. pHlndicator ~
EXAMPLES: paper", _ Th\
Glycine, methionine ~ ' =-..
FLINN METHOD oo 0
#5 AMINES, AROMATIC
Aromatic amines are rel atively toxic and flammable materi als.
Depending on the material , there are several disposal routes. Small
ED
quantities of aromatic amines «500 g) can be disposed of by incin-
eration (see Flinn Disposal Method #26c). Many common dyes and Neutralize the mixture by adding solid sodium carbonate or 1 M
pigments contain aromatic amine groups and do not present any sodium hydroxide solution .
unusual problems for incinerat ion or burial in a landfill. Please
consult your local authorities and Flinn Disposal Method #26a. FLINN METHOD #5 continued on next page.
Three common aromat ic ami ne s, p yrid in e, anilin e, and
diphenylamine , can be destroyed by oxidation with potassium
permanganate. Please ... Read the Narratives
EXAMPLES:
Aniline, pyridine, and diphenylamine Important narratives precede these specific chemical
disposal methods! Please read each narrative carefully!
MATERIALS REQUIRED: Do not use these procedures if you are not comfortable
Chemical-resistant gloves with the chemistry. Do not use these procedures without
Chemical-resistant apron
first consulting with your local government regulatory
Chemical splash goggles
officials. These procedures may not be used in some
Fume hood
Magnetic stir plate and stir bar jurisdictions. These procedures may be dangerous.
1-L beaker Once again ... read the narratives that precede these
pH indicator paper specific chemical disposal methods.
3 M sulfuric acid
FLI"" ,SCIE"TIFIC I"C. ________"Yc_o_ur_S_afl_er_S_o_ur_ce_ fl_or_S_c/_'en_c_e _Su...p...p'_ie_s"
FLINN METHOD #5 continued "supernatant liquid," and merely means the liquid above a solid
sitting on the bottom of a container. You really don 't have a super-
natant liquid until the solid has settled , but rather a suspension of
the solid . Thus a supernatant liquid will be clear, not cloudy, and
rather than filtering, can be carefully poured off or decanted.
b. The other substances in this class all form insoluble calcium
Sodium Sulfite ~ •
compounds, either calcium fluoride, calcium tungstate or calcium
molybdate, with the reaction of the target compound and calcium
chloride. These insoluble compounds are judged to be innocuous,
and may be sent to a landfill.
o
~---
~ PROCEDURE A:
Add solid sodium bisulfite or
sodium sulfite until the purple For Hydrogen Fluoride (Hydrofluoric Acid) Disposal
. --- ~Adduntil
color disappears.
~ .- -
... -.-; ~
; solution clears
~
Filtration apparatus /'
i
Dilute
CHEMICAL CONCEPTS: HCI
a. For hydrogen fluoride (hydrofluoric acid): By reacting the hydro- '.
fluoric acid with calcium hydroxide, two purposes are accomplished "
simultaneously. The acid is neutralized and the fluoride is converted
to the very insoluble calcium salt, which precipitates as a white When the addition is complete, c heck the pH of the resulti ng
solid. mixture with pH indicator paper. Neutralize the mixture to pH 7
2HF + Ca(OHh -7 2H 20 + CaF2 with dilute hydrochloric acid. This will dissolve most of the excess
After neutralizing the excess calcium hydroxide with hydrochloric calcium hydroxide. Do not make th e solution acidic, as this will
acid , the calcium fluoride is allowed to settle to the bottom of the increase the solubility of the calcium fluoride just precipitated .
reaction container. The liquid above contains calcium ion and chlo-
ride ion, which are both innocuous. This liquid is referred to as the FLINN METHOD #6 continued on next page.
1-800-452-1261 Chemical Disposal Procedures
Filter or decant off the supernatant liquid. Flush the liquid down the
drain with excess water.
PROCEDURE B:
pH Indicator ~
Paper
~ - ~\ " ' - --
Please ... Read the Narratives
~ III1I1U
Important narratives precede these specific chemical
{' ~ disposal methods! Please read each narrative carefully!
r---w Do not use these procedures if you are not comfortable
~ with the chemistry. Do not use these procedures without
3M first consulting with your local government regulatory
L
~
or HCI officials. These procedures may not be used in some
jurisdictions. These procedures may be dangerous.
Once again ... read the narratives that precede these
Adjust the pH to 7 using pH indicator paper by adding 3 M sodium specific chemical disposal methods.
hydroxide or hydrochloric acid as necessary.
FLinn SCIEnTIFIC Inc. ________"Yc_o_ur_S_afl_er_S_o_u"_ce_ fl_or_S_cl_·en_c_e _su_p...p'_ie_s"
FLINN METHOD
#8 AZIDES AND AZO- COMPOUNDS
Azides should NOT be drain-disposed. Drain disposal not only
contaminates sewer water, but azides can also react with lead and
copper in drain lines, solder joints and brass fittings. These metal
azides remain resident in the sewer system , and are unstable and
explosive. Drain systems have been destroyed by such explosions.
In addition, azides are not biodegradable and kill the necessary
bacteria present in the digestion system of wastewater treatment
plants. Stocks of these materials should be kept low. Note that the
order of addition, nitrite before acid, is important; if the order is
reversed , acidifying before adding the nitrite, the result will be the
evolution of extremely poisonous HN 3 , hydrazoic acid.
e
Slowly, and with continuous stirring, acidify the solution with 3 M
EXAMPLES: sulfuric acid , checking with indicator paper as you add . The pH
Sodium azide, triphenyl tetrazolium chloride should not go below 5.
MATERIALS REQUIRED:
Chemical-resistant gloves
Chemical-resistant apron
Chemical splash goggles or full-face shield
Efficient hood
Magnetic stirrer and stir bar or glass stirring rod
3 M sodium nitrite solution, in a 50% molar excess
3 M sulfuric acid
Large glass beaker
pH indicator paper
Potassium iodide-starch test paper
CHEMICAL CONCEPT:
The azide ion reacts with the nitrite ion in the presence of acid to
form nitrous oxide, nitrogen and water:
4N 3- + 2N02- + 6W -7 6N 2 + N20 + 3H 20 o
Allow the mixture to stand, periodically checking with potassium
Nitrous oxide is poisonous in large quantities. (Nitrous oxide is
iodide-starch paper. The decomposition is complete when the
also known as laughing gas, and in small quantities is a general
potassium iodide-starch paper turns blue.
anesthetic.) The reaction proceeds best in a weakly acidic solution,
but is still slow. The azide ion is a strong reducing agent, and will
preferentially react with the nitrite ion. Only when azide is consumed
will iodide ion from the potassium iodide-starch test paper be
oxidized by the nitrite ion to iodine. The iodine produced will form
the familiar blue complex with starch . Thus, the presence of blue
color on the potassium iodide-starch test paper indicates that all the
azide has been consumed.
PROCEDURE:
o
This procedure is intended only for small
quantities. Good ventilation is required for this No Disposal Required!
procedure since toxic nitrogen oxides are
evolved. Dissolve the inorganic azide in Flinn sodium is packaged
enough water to make the azide concentration 5% or less. ready-to-use and ready-
to-store. Five small pieces
of sodium (0.3-0.5 g each),
perfect for demonstrations,
are packaged under mineral
oil in a PVC-coated glass
bottle, in a plastic bag
and then a metal can for
safer storage.
Count on Flinn for smaller
Slowly add 3 M sodium nitrite package sizes to eliminate
solution , while stirring , until disposal problems.
there is a 50% molar excess
over the amount of azide.
1-800-452-1261 Chemical Disposal Procedures
PROCEDURE B:
FLINN METHOD
#9 CARBON DISULFIDE
Carbon disulfide is a highly volatile, highly toxic , and flammable
solvent. Extreme care should be taken when handling and dispos-
ing of this material. Large quantities should be incinerated (see
Flinn Disposal Method #26c). Smaller quantities may be evapo- Work in a hood. Add 7 L of
rated or reacted with bleach to form sulfuric acid . laundry bleach or a calcium
MATERIALS REQUIRED: hypochlorite solution [550 g
Chemical-resistant gloves Ca(OClh in 2.5 L of water) to a
Chemical-resistant apron large bucket or container.
Chemical splash goggles or full -face shield
Efficient hood or outdoor site
Dry chemical (ABC) fire extinguisher
Iron or glass pan (procedure A)
For Procedure B
Large bucket or similar container
Laundry bleach or calcium hypochlorite
Thermom eter
Magnetic stirrer and stir bar or stirring rod 8:00 O'Clock
CHEMICAL CONCEPT:
Bleach (sodium hypochlorite) is a strong oxidizing agent and will
oxidize carbon disulfide to carbon dioxide and sulfuric acid.
CS 2 + BOCI- + H2 0 ~ CO 2 + 2H2 S0 4 + BCI-
For each 0.5 mole (3B g, 30 mL) of carbon disulfide, 5 moles
(25 % excess) hypochlorite is required. Laundry bleach (7 L) or
calcium hypochlorite (550 g Ca(OClh in 2.5L of water) solution
are suitable sources of hypochlorite. Th e reaction temperature
must be maintained between 20-30 °C to avoid evaporation of th e
carbon disulfide.
10:00 O'Clock
o metals present (in addition to silver) will also precipitate, e.g., lead
-
as lead chloride. If your silver is still relatively pure and you wish to
Prepare a dilute solution of (1 M or <10%) base by diluting the prepare AgCI , you want to stop after this step (step 2a).
solution or dissolving the solid into water. Considerable heat may be Ag+(aq) + CI-(aq) ~ AgCI(s)
involved when dissolving a solid base. It is wise to experiment with To produce silver metal, the silver chloride is dissolved in a strong
a small quantity to determine the heat generated , and if an ice/water base (NaOH) and heated. Sucrose is then added to this mixture. The
slush is required . disaccharide sucrose will hydrolyze in a strong base to the mono-
saccharides fructose and glucose. Fructose is an alpha-hydroxy
pH Indicator ketose; glucose is an aldose. Both of these substances, i.e., fruc-
tose and glucose will reduce silver ion to silver metal. Silver will be
Paper ~
formed as a heavy gray precipitate.
~~ The last step has the precipitate being redissolved in nitric acid.
Silver oxide is precipitated upon addition of sodium hydroxide. The
1IIIIIn substance should be quite pure since other cations and anions
7 ~ would have stayed in solution during the prior processes.
Ir -----ijl
~
(Disposal method)
~~;;~______~
i 6M I
Hel
The silver is precipitated as silver chloride, using cheap sodium
chloride. Although silver chloride is not as insoluble as silver sulfide,
o "
When solution is complete, slowly add 3 M hydrochloric acid until
it is insoluble enough so that any silver ion that may leach from silver
chloride in a landfill will be of such small concentration as to
produce no hazard, and would probably react to form silver oxide
in any case.
the mixture is neutralized. Check with pH paper. More heat may be
evolved in the neutralization process. FLINN METHOD # 11 continued on next page.
1-800-452-1261 Chemical Disposal Procedures
PROCEDURE A:
A Silver Recovery Process Presented as a " Recipe"
.etJ
reclamation procedure , you may dispose of so luble silver
compou nds by the next procedure.
FLINN METHOD #11 continued on next page.
{-II substance that is inexpensive and will destroy the oxidizing power
before disposal. Such a SUbstance is sodium thiosulfate. This reac-
tion proceeds best in weakly acidic solutions. (Too much acid wi ll
----.-:- react with the sodium thiosulfate directly, precipitating elemental
sulfur from the mixture.) In the example below, the thiosulfate ion
reacts with the bromate ion to produce innocuous sulfate ion and
....
~
7
lUlU
~
III
~:
Allow the precipitate to
dry and dispose of it in a
bromide ion. Any excess acid is neutralized with base before flush-
ing down the drain.
PROCEDURE:
3H 2 0 + 3S 20 3-2 + 4Br03- ~ 6S0 4- 2 + 4Br- + 6W
o
This method is
for small quanti- 50% Na,5,03
Flush the supernatant
ties of laboratory
liquid down the drain
oxidizing agents
with a 20-fold excess
only. It is best to experiment with a small por-
of water.
tion of the amount you wish to destroy before
undertaking the entire amount. See note on
next page for iodine (solid). Add the material to
a twofold excess of a 50% aqueous solution of
sodium thiosulfate (hypo) with continuous stirring .
FLINN METHOD #12a continued on next page.
1-800-452-1261 Chemical Disposal Procedures
pH Indicator Paper
C9
12:00 O'Clock
o
Add 3 molar sulfuric
acid while stirring to
bring the pH in the
Strong reducing agents will react vigorously with oxidizing agents to
produce heat and possibly fire . Some reducing agents may cause
a fire when in contact with moist combustible materials. A simple
oxidation reaction will render reducing agents safe for disposal.
~.
range of 2-3. Check EXAMPLES:
with indicator paper. A Potassium nitrite, sodium sulfite, sodium thiosulfate
temperature rise indi-
cates the reaction is MATERIALS REQUIRED:
proceeding. Add more Chemical-resistant gloves
~
3 molar sulfuric acid as Chemical-resistant apron
necessary to produce Chemical splash goggles or full-face shield
such a rise. Allow the Sodium carbonate, Na2C0 3
mixture to stand for Sodium hypochlorite solution (bleach)
about one hour. Ammonium hydroxide, NH 40H (proc. 8)
>-------
3 M hydrochloric acid, HCI (proc. 8)
Large glass beaker
Glass stirring rod 1 M sodium hydroxide solution
pH indicator paper 1 M hydrochloric acid
CHEMICAL CONCEPT:
Reducing agents by definition reduce other substances; that is,
they readily change the oxidation state of a substance from a high
value to a lower value. They are the opposite of oxidizing agents.
e
Again check with pH
(See the discussion on oxidizing agents under Chemical Concept in
Flinn Disposal Method #12a Oxidizing Agents.) In the example
involving carbon reacting with oxygen, the oxygen was the oxidiz-
paper. Neutralize the ing agent because it oxidized the carbon. On the other hand , in this
solution with either so- same reaction, carbon is the reducing agent, because it changed
lillllil 11111111 dium hydroxide solution the oxidation state of oxygen from zero to negative 2 (-2). In the
( ~ ( ~ or sodium carbonate process considerable heat is produced.
rr---tiI Ir - - - i jl
solution. We recommend that reducing agents be safely reacted with a
I ~OHHN~
substance that will destroy the reducing power before they are
disposed of. One such substance is bleach or sodium hypochlorite.
This works best in a weakly basic solution , and a cheap base is
sodium carbonate. So first , dissolve the reducing agent in water,
'" then make it basic with sodium carbonate, and finally react it with
the hypochlorite ion. After the material is oxidized, the pH is
o
The residues from the above
adjusted to neutral and the resulting mixture which contains innocu-
ous ions is flushed down the drain. In the example below, sulfite ion
reacts with hypochlorite ion to produce sulfate and chloride ions, all
procedure must undergo further in aqueous solution .
treatment if they contain
S03-2 + CIO- -7 S04-2 + CI-
chromium or manganese. The
products from the reduction of Nitrites are a unique class of compounds in that the nitrogen is in
chromates, dichromates , and an intermediate oxidation state (+3). It can be either oxidized to the
permanganates are insoluble +5 state (N0 3-) or reduced to a lower state (NO or N2). Nitrites are
manganese dioxide or chrom- easily destroyed by adding 50% excess ammonia and acidifying to
ium hydroxide. These materials pH 1. The resulting product is nitrogen gas.
can be removed by filtration and HN02 + NH/ -7 N2 + 2H 20 + W
must be treated by Flinn Disposal Note: The astute teacher may realize from the above discussions
Method #27f before final disposal. Do
not dump chromium salts down the drain.
of oxidizing and reducing agents that the way to dispose of these
substances is to react a substance from one class with a substance
from another class. Think through the chemistry, and if you feel
iii
• : •
comfortable with it, try this "shortcut" of two processes compressed
into one. You will also save costs of the other chemicals required.
Always use small quantities when trying a new reaction, and be sure
Flush other solutions down you know what products you will get and any potential hazards
the drain with large quantities associated with them.
of water.
FLINN METHOD #12b continued on next page.
Dissolvewate
distilled the in organic
. nitrite salt in
CD r.
disti~e~um re~uequal
In the
of s d'large b eaker, dissolve
carbonate and
water. amount
clng agent in
NaOCI
8:00 O'Clock ~
C9 pHl,d;~", "'"
C9
12:00 O'Clock
12 00 O"Clod< \~
EI$
Che
ck the mixture with
sary. Useif sodium
solution
~ .
pH Indicator
basic . hydroxide
"
laci~·nd
solutionpa er IC, or
" "
neutralize as neces-
hydrochloric acid
Q)
Using pH i d'
with 3 M hydrochloric
n Icator paper
acidto mea
. SfIr f or
sure,
"
.
two aCidify
hours.
..
the soluf Ion to pH 1
2:00 O'Clock
~"j\\
solution down the dr~i~~~:~o~,xcess
Check the pH of th
neutralize
water. if necessary. Wash the
1-800-452-1261 Chemical Disposal Procedures
Thermometer PROCEDURE:
o
Add th e mercaptan or sulfide slowly whi le stirring . The reaction
usually starts quickly, as evidenced by a temperature rise and
disappearance of the mercaptan. Maintain the temperature at about
50 °C by varying the addition rate as necessary. When the addition
is complete (it may take an hour), allow the mixture to come to room
o
Thi s procedure must be done in a fum e hood.
temperature and stand overnight. Fill a large beaker '/2 full of water, and using pH
indicator paper, make it basic (at least pH 12)
with 3 M sodium hydroxide solution .
o
Flush the neutral material down the drain with a 20-fold excess
jurisdictions. These procedures may be dangerous.
Once again ... read the narratives that precede these
specific chemical disposal methods.
of water.
FLI"" lCIE"TIFIC I"C. ________"Yc_o_ur_S_a_fer_ S_O_UIi_Ce_ "_or_S_cl_·en_c_e _Su...p...p'_ie_s"
FLINN METHOD #14 continued PROCEDURE:
3O%Ca(OClh
o
While stirring , slowly add the sodium hypochlorite solution (about
100 mL per g CN) or 30% calcium hypochlorite solution (20 mL per
g CN). Heat may be evolved; maintain the temperature below 50 DC
by using an ice bath if necessary. Once the addition of hypochlorite
is completed (use a twofold molar excess), allow the mixture to
stand for several hours.
o FLINN METHOD
..
Flush the mixture down the drain with a 20-fold excess of water.
# 16 HYDRAZINES AND THEIR SALTS
Hydrazines contain a nitrogen-nitrogen single bond and as a result
are very reactive. Many hydrazines are also toxic and/or carcino-
genic. Phenyl hydrazine is the only chemical in this class that is
FLINN METHOD routinely found in high school science laboratories and is less reac-
tive and less toxic than many lower molecular weight hydrazines. It
#15 ETHERS does need to be neutralized by chemical means before disposal.
Bottles of ethers that have been opened and are more than a year EXAMPLE:
old may contain hazardous quantities of explosive peroxides. These Phenyl hydrazine
bottles should not be opened and should be disposed of by the MATERIALS REQUIRED:
appropriate authorities. Chemical-resistant gloves
EXAMPLES: Chemical-resistant apron
Diethyl ether, dioxane, tetrahydrofuran Chemical splash goggles or full-face shield
Fume hood
MATERIALS REQUIRED: Large glass beaker
Chemical-resistant gloves Magnetic stir plate
Chemical-resistant apron Calcium hypochlorite, Ca(OClh, tenfold molar excess
Chemical splash goggles or full-face shield
Efficient hood or outdoor site CHEMICAL CONCEPT:
Dry chemical (ABC) fire extinguisher This procedure is similar to #14. The phenylhydrazine is oxidized by
Iron or glass pan hypochlorite to benzene, nitrogen, and salt.
CHEMICAL CONCEPT: C6HsNHNH2 + OCI- ~ C6Hs + N2 + NaCI + H2 0
No concept statement judged necessary for this procedure. FLINN METHOD #16 continued on next page.
1-800-452-1261 Chemical Disposal Procedures
PROCEDURE:
o
This procedure must be done in a fume hood .
Dissolve the substance to be disposed of in a
20-fold excess of water in the beaker.
o
Slowly add solid calcium hypochlorite (1 g per g hydrazine) while
natural air movement in the hood to
evaporate the material. If you do not have a hood , the evaporation
may be done outdoors, but it is required t hat the process be
sti rrin g; monitor the temperature of the solution. It should rise, but attended at all times.
if the solution becomes very hot, reduce the rate of addition of If neither of the above options is appropriate, the materials can be
calcium hypochlorite. burned (see Flinn Disposal Method #26c).
FLINN METHOD
e
Abou t t wo hours after com pl etion of the add it ion of calc iu m
EXAMPLES:
Naphthalene, benzophenone, butyl stearate
hypochlorite, flush the mixture down the drain with a 20-fold excess
of water.
FLINN METHOD
# 22a PEROXIDES, INORGANIC
If you are dealing with sodium perox-
Inorganic peroxides are strong oxidizing agents. When in contact or ide, first break up any lumps with a
mixed with organic or combustible materials, fires or explosions are dry glass stirring rod or a plastic
possible. Do not throw these materials in the trash. spoon .
EXAMPLES:
Hydrogen peroxide, sodium peroxide
MATERIALS REQUIRED:
Chemical-resistant gloves
Chemical-resistant apron
Chemical splash goggles or full-face shield
Large beaker, % full of water
Plastic spoon (optional)
Glass stirring rod
Pour the material slowly with
pH indicator paper
continuous stirring into a large H20
1 M sodium metabisulfite, Na2S20 S
beaker of water. Oxygen gas will
3 M hydrochloric acid , HCI
evolve and the solution will
CHEMICAL CONCEPT: become strongly basic. The final amount of sodium peroxide in
Hydrogen peroxide is destroyed by reducing with sodium meta- the water should be no more than 5%. (If you have more sodium
bisulfite or diluting it with water to less than 3% and flushing it peroxide than will fit into this concentration in your beaker, do the
down the drain. procedure again until all the material is disposed of.)
Sodium peroxide reacts violently with water to form oxygen gas
and sodium hydroxide. Because of this reaction, sodium peroxide
is stored in sealed containers to avoid reaction with moisture in the
air. With fresh sodium peroxide the reaction with water is quite
exothermic, but if used from a previously opened container, it may
be less vigorous. Old sodium peroxide may have already slowly
converted itself to sodium hydroxide. Test the materials for reactiv-
ity by adding a small amount (0.1 g) to water. Evolution of oxygen
indicates an active peroxide which should be reduced prior to
disposal.
Na20 2 + H20 --? 2NaOH + %0 2
Na20 2 + Na2S20 S+ H20 --? 2NaOH + NaHS04
3M Using pH indicator paper as a
PROCEDURE A: Water Dilution Hel monitor, neutralize the solution
with 3 M hydrochloric acid.
PROCEDURE:
Using pH indicator
paper as a monitor,
neutralize the solution
with 3 M hydrochloric
acid. o
Pour the material into the 3 M sodium hydroxide solution . Allow to
stand at least 24 hours, stirring frequently. Benzoyl peroxide has low
water solubility, so frequent agitation is important to bring the
decomposition reaction to completion.
o
Using pH indicator
paper as a monitor,
neutralize the solution
with 6 M hydrochloric
acid.
FLINN METHOD
o
Slowly add sodium hypochlorite solution (bleach) to the inorganic
sulfide. Add 200 mL bleach for each 10 mL of ammonium sulfide or
5 g of sodium sulfide.
o
Flush the neutral solution down the drain with excess water.
FLINN METHOD
# 23 SULFIDES, INORGANIC
Inorganic sulfides release highly toxic hydrogen sulfide gas on treat-
ment with acid . These materials should not be disposed of in the
trash or drain.
e
Allow the solution to sit overnight in the fume hood. Flush the entire
solution down the drain with a 20-fold excess of water.
EXAMPLES:
Sodium sulfide, ammonium sulfide Note: This procedure is not intended for use with hydrogen sulfide
MATERIALS REQUIRED: gas. Gas cylinders are best if used completely, vented in an oper-
Chemical-resistant gloves ating fume hood for several hours, then disposed of in the trash.
Chemical-resistant apron Small lecture bottles cannot be reused.
Chemical splash goggles or full-face shield
Efficient hood or excellent ventilation
Large glass beaker
Glass stirring rod FLINN METHOD
Sodium hypochlorite solution, NaOCI, (laundry bleach)
0.5 M sodium hydroxide solution, NaOH #24a ACIDS, ORGANIC
CHEMICAL CONCEPT: Organic carboxylic acids can be disposed of by neutralization, solid
Inorganic sulfides are easily oxidized to sulfate using hypochlorites waste disposal, and incineration. Water-soluble organic acids are
as an oxidizing agent. best disposed of by reacting with a base to form water soluble
Na2S + 40CI- -7 Na2S04 + 4CI- sodium salts. Long alkyl chain carboxylic acids (e.g ., lauric ,
A small amount of base is added to keep the solution basic. A decanoic) and their salts are insoluble in water, but small quantities
basic solution is needed because inorganic sulfides react with acid pose little risk to the environment. These can be disposed of using
to produce highly toxic hydrogen sulfide gas and the hypochlorite Flinn Disposal Method #26a. All other organic acids are best
is more stable at a higher pH . disposed of by incineration (Flinn Disposal Method #26c).
The products from the reaction are sulfate salts which are Use neutralization method for:
nonvolatile, odorless and have low toxicity. These materials can be Acetic acid
flushed down the drain. Acetic anhydride
(Use NaOH only; the decomposition may be slow)
_ PROCEDURE: Aceto-orcein solution
Barfoed 's reagent
(Copper carbonate may be formed. Filter and landfill.)
Formic acid
Fumaric acid
Lactic acid
Malonic acid
Oxalic acid
Propionic acid
Succinic acid
Tartaric acid
Trichloroacetic acid
MATERIALS REQUIRED
Chemical-resistant gloves
Chemical-resistant apron
Chemical splash goggles or full -face shield
Fume hood or excellent ventilation
o
This procedure must be performed in a fume hood. Dissolve the
Large glass beaker
Glass stirring rod
Sodium carbonate or 3 M sodium hydroxide solution
inorganic sulfide in 0.5 M NaOH solution. For ammonium sulfide, pH indicator paper
use 100 mL of NaOH solution for every 10 mL of sulfide solution. FLINN METHOD #24a continued on next page.
1-800-452-1261 Chemical Disposal Procedures
PROCEDURE:
o
... neutralizing the resu lting solution w ith sodium carbonate or
sodium hydroxide solution , checking the pH with pH paper. Stir the
solution until all solid organic acids have dissolved.
o
Dilute the acid by pouring it into a large beaker containing water. The
final concentration of the acid should be 1 M or less.
e
Rinse the solution down the drain with an excess of water.
Do not use these procedures if you are not comfortable
with the chemistry. Do not use these procedures without
first consulting with your local government regulatory
officials. These procedures may not be used in some
jurisdictions. These procedures may be dangerous.
Once again .. . read t he narratives that precede these
specific chemical disposal methods.
FLI"" ,SCIE"TIFIC I"C. ________'_'yo_u_r _Sa_fe_r_S_ou_rc_e_fo_r_S_cie_n_ce_ S_u...p...p'_ies_"
FLINN METHOD #24b continued PROCEDURE:
8:00 O'Clock
12:00 O'Clock
o
Flush the neutral mixture down the drain with a 20-fold excess
Using pH indicator
paper, neutralize the
of water. solution with 3 M
hydrochloric acid.
FLINN METHOD
#25 CARBIDES
Calcium carbide reacts with small quantities of water to generate
acetylene, a highly flammable gas. Decomposition under controlled
conditions will produce acetylene which can be vented to a fume
hood for safe disposal.
EXAMPLE:
Calcium carbide o
Decant the neutral solution off, and flush it down the drain with a 20-
MATERIALS REQUIRED: fold excess of water.
Chemical-resistant gloves
Chemical-resistant apron
Chemical splash goggles or full-face shield
Fume hood or outdoor site
Large glass beaker % full of water
Glass stirring rod
Dry chemical (ABC) fire extinguisher
3 M hydrochloric acid
o
Dry any remaining precipitate, and
pH indicator paper
package it for disposal in a landfill
CHEMICAL CONCEPT: suitable for chemical wastes.
Calcium carbide reacts with water to form acetylene gas and
calcium hydroxide, which is not very soluble in water. The addition
of hydrochloric acid to the suspension of calcium hydroxide will
dissolve it, forming water and calcium chloride. This solution may be
flushed down the drain.
CaC 2 + 2H 20 -7 C2H2 + Ca(OHh
Ca(OH)2 + 2HCI -7 CaCI 2 + 2H 20
1-800-452-1261 Chemical Disposal Procedures
FLINN METHOD
#27b MERCURY METAL
PROCEDURE:
Mercury metal must not be disposed of by any means except to
return it to a supplier for recycling. Mercury Waste Solutions, Inc.
o
Absorb high-boiling liquids onto vermiculite or
(1-800-741-3343) is a major mercury recycler and may be a disposal
option. Under no circumstances should any other method of
disposal be attempted . Metallic mercury is never buried , burned ,
paper towels and place in a cardboard box. placed down a drain or otherwise put into the environment. For
Dissolve solids in a suitable flammable solvent disposal of mercury compounds, please see Flinn Disposal
(such as ethyl alcohol , acetone, or kerosene) . Methods #27d or #27f, depending on the compound.
1-800-452-1261 Chemical Disposal Procedures
FLINN METHOD
#2 7C PHOSPHORUS, RED AND WHITE (YELLOW)
Phosphorous is a highly reactive and very flammable material.
Yellow (also called white) phosphorous is pyrophoric, a poison, and
ignites spontaneously in air. Red phosphorous is not pyrophoric but
is very flammable and can react explosively with strong oxidizing
agents. Both chemicals must be handled and disposed of with
utmost care.
EXAMPLES:
Yellow and red phosphorous
MATERIALS:
Chemical-resistant gloves
Chemical-resistant apron This procedure must be performed in a fume
Chemical splash goggles or full-face shield hood. Add 1 g of red phosphorous to a 1-L
Spatula or wedge glass beaker containing SOD mL of O.S M
Heavy plastic bag sulfuric acid . Stir the solution .
Procedure A
Fume hood
1-L glass beaker
Magnetic stirrer and stir bar
O.S M sulfuric acid
Add 12 g of potassium bro-
Potassium bromate, KBr03
Sodium metabisulfite, Na2S20 S mate while stirring . Stir the
mixture until all the phospho-
Procedure B rous has dissolved. This step
Heavy iron pan may take as long as 24 hours.
Sodium carbonate, (soda ash), Na2C03 If all the phosphorous is not
Dry sand or a Class D fire extinguisher dissolved in 24 hours, add
Outdoor site for burning more potassium bromate.
Scrap wood
Shredded paper
Matches
CHEMICAL CONCEPT:
Phosphorous is oxidized under controlled conditions to phosphoric
acid. Red phosphorous requires a twofold molar excess of aqueous
potassium bromate for the oxidation reaction.
The reaction time for the oxidation of red phosphorous depends
on the physical characteristics of the phosphorous. Large lumps of
phosphorous may take up to 24 hours to completely dissolve and When all the phosphorous
react. Smaller pieces will take less time. has dissolved, add 16 g of
6P + SKBr03 + 9H 20 --7 6H 3P0 4 + SKBr sodium metabisulfite.
The excess borate should be reduced by sodium bisulfite before
final disposal down the drain.
The oxidation of yellow phosphorous is extremely time consum-
ing (requires over a week for complete oxidation) and may generate
toxic by-products. We do not recommend the oxidation of yellow
phosphorous as a disposal method in high school laboratories.
Yellow phosphorous ignites spontaneously in air and is converted
to phosphorous pentoxide. Allowing small quantities of yellow phos-
phorus to ignite in air may be the best disposal route for schools.
This procedure should only be used for small «2S g) quantities of
yellow phosphorous. Flush the solution down
the drain with a 20-fold
PROCEDURE A: Red Phosphorus excess of water.
~
Reid PhodsPhorus. is, inII f~ct, red in
~
~ _ "'-
Please ... Read the Narratives
co or an was onglna y In power d . Important narratives precede these specific chemical
or lump form . Most frequently, it is ~ disposal methods! Please read each narrative carefully!
packaged in a metal can . If the can - ~
has been stored a long time, it is likely
that the contents have taken on mois-
1, Do not use these procedures if you are not comfortable
with the chemistry. Do not use these procedures without
first consulting with your local government regulatory
ture, forming phosphoric acid and are
attacking the can. Your first task is to get this "mess" under control.
officials. These procedures may not be used in some
The can may be stuck to the shelf. Using the spatula or wedge, pry jurisdictions. These procedures may be dangerous.
the can loose and place it in a heavy plastic bag. You have now Once again ... read the narratives that precede these
provided it with a safer home while you examine the options to get specific chemical disposal methods.
the material off the premises.
FLI"" ,SCIE"TIFIC I"C. ________'_'yo_u_r _Sa_fe_r_S_ou_rc_e_fo_r_S_ci_en_c_e _Su....p...pl_ie_s"
FLINN METHOD #27c continued
FLI NN METHOD
PROCEDURE B: White or Yellow Phosphorus #2 7d ANTIMONY, ARSENIC, VANADIUM AND
THEIR COMPOUNDS: CADMIUM AND
OTHER HEAVY METALS AS ELEMENTS
White phosphorus and yel- This procedure has been combined with Flinn Disposal Method
low phosphor us are two #27f. Please refer to the following procedure.
names for the same sub-
stance. The yellow form has
some co lored impurities.
This material is a waxy solid ,
usually in the form of a stick.
It is stored under water at all
times, as it is extremely reac-
VISIT OUR
tive with air. It may be in a WW.". ,,,. WEBSITE
glass jar inside a metal can, • .nnSCi.COIJJ
or just in a metal can. You
have two disposal options:
removal by professionals or
burning at a remote site. If you choose professional removal , make
sure the phosphorus is completely submerged in water, in a glass
container with a plastic cap. Place this glass container inside a
metal container packed with vermiculite or bentonite. Label the can FLINN METHOD
clearly. Give it to the professional. Call us if we can help you further. # 2 7f HEAVY METALS AND THEIR SALTS
AND COMPOUNDS
The heavy metal elements have limited reactivity and low solubility
in water. These materials, while in metallic form are less hazardous.
Examples include lead, antimony, cadmium, chromium, cobalt, and
White or Yellow nickel metals.
Phosphorus Heavy metal salts are very soluble in water, extremely toxic, and
accumulate in body tissues. The soluble salts must be converted
\
I
into a stable, insoluble salt that can be buried in a landfill approved
Class 0
for disposal of hazardous wastes. Heavy metal cations that are
~e ~~';~'
suitable for this procedure include antimony, arsenic, cadm ium,
chromium, cobalt, lead , mercury, and nickel. This proced ure
converts them into their most insoluble form , and we believe it is
appropriate to bury the resulting solids in a landfill approved for the
disposal of hazardous waste. As always, check with your local
You may choose burning if landfill operator about proper disposal procedures.
your quantity is less than 25 grams
or so. It is unlikely that atmospheric EXAMPLES:
contamination from this amount of material should cause concern. Lead nitrate, arsenic trioxide, mercuric chloride
Transport the material in its original container, along with a heavy MATERIALS REQUIRED:
iron pan and a Class 0 fire extinguisher or dry sand to a remote site. Chemical-resistant gloves
Chemical-resistant apron
Chem ical splash goggles or full-face shield
Efficient hood
Large beaker
Glass stirring rod
3 M hydrochloric acid
3 M sodium sulfide solution
0.5 M sodium silicate solution
(prepare by diluting 1 part Water Glass solution (S0102) with
7 parts water)
pH indicator paper
1 M sulfuric acid
3 M sodium hydroxide solution
Filtration apparatus
Plastic container with screw-top, size dependent on
Class 0 amount of material
Fire Extinguisher CHEMICAL CONCEPT:
Heavy metal ions react with sulfide ion to precipitate extremely
Pour off the water coveri ng the phosphorus, and place the phos- insoluble sulfide solids. The sulfides are somewhat more soluble in
phorus in the iron pan . Set the pan on the ground. As the water acidic solution, so it is wise to make sure the pH is ~7 after the
evaporates from the surface of the phosphorus, it will start to react precipitation of the sulfide is complete. If the supernatant liquid
with oxygen in the air. The phosphorus will slowly heat up, due to tests basic, do not bother adjusting the pH.
the spontaneous reaction, and begin emitting enormous volumes of Hg+2 + S-2 ~ HgS (solid)
white smoke. This smoke is phosphorus pentoxide and is very A second procedure is also available that converts soluble metal
acidic. Do not breathe this smoke. Stay upwind until the smoke salts to insoluble metal silicates. This procedure is recommended
subsides. for cadmium , antimony, and lead salts. Metal silicates are less reac-
tive than metal sulfides and equally insoluble.
Do not burn any substance without first checking with local
authorities to be sure that burning is permitted. Do not burn in an Cd+2 + Si0 3- 2 ~ CdSi0 3 (solid)
urban setting, or if burning will affect the school's neighbors. FLINN METHOD #27f continued on next page.
1-800-452-1261 Chemical Disposal Procedures
PROCEDURE B:
8:00 O'Clock
..
precipitation of the
metal sulfide.
Adjust the pH to
around 10 with a few
drops 1 M sulfuric acid.
Stir for 1 hour.
o
Dissolve the solid barium salt in a
minimum amount of water. (Barium
Collect the precipitate by filtration .
carbonate and barium peroxide
Allow the filtrate to dry.
are not soluble in water, so just
suspend them in a tenfold excess
of their weight in water.)
FLINN METHOD
#27 h BARIUM COMPOUNDS
Soluble barium salts are extremely toxic and should not be flushed
down the drain or buried in a landfill. Conversion to an insoluble
barium sulfate is the best disposal route.
EXAMPLES:
All barium salts, i.e., barium nitrate, barium hydroxide,
barium chloride
MATERIALS REQUIRED:
Chemical-resistant gloves
Chemical-resistant apron
o
-
Chemical splash goggles or full-face shield
Large beaker The liquid will be
Glass stirring rod acidic; using pH indi-
3 M sulfuric acid cator paper, neutralize
Filtration apparatus (optional) it with sodium carbon-
Wide-mouth plastic container with screw top ate and flush it down
pH indicator paper the drain with excess
Sodium carbonate, Na2C03 water.
CHEMICAL CONCEPT:
In contrast to the metal ions mentioned in #27f above, barium
sulfide is rather soluble. However, barium sulfate is highly insoluble.
This procedure produces barium sulfate in an acidic solution. Note
that the only acid which will work in this procedure is sulfuric acid.
The acid serves a double purpose in the case of barium hydroxide
and barium peroxide, in that it neutralizes the hydroxide ion in addi-
tion to its primary purpose of furnishing sulfate ion to react with the
barium ion. Once the precipitation is complete, the precipitate is
o
Allow the precipitate to dry, place it in a plastic bag
separated from the supernatant liquid and any excess acid is
and then in a plastic container, and bury the
neutralized with sodium carbonate. The solid barium sulfate is put
container in a landfill suitable for such waste.
in a landfill, and the neutralized supernatant liquid is flushed down
the drain.
Ba+2 + SO.-2 ~ BaSO. (solid)
2W + C0 3- 2 ~ CO 2 (gas) + H20
1-800-452-1261 Chemical Disposal Procedures
FLINN METHOD
o
This method is recommended for small quantities only. Pour a shal-
returning chemicals to their containers.
12. Never store chemicals or solutions in "home-
low layer of the substance into the pan , and place it under an
made" bottles.
efficient hood or in an appropriate outdoor site. 13. Purchase chemical demonstration kits or
chemistry student kits that contain exact quan-
tities of chemicals.
14. Prepare only enough solution for immediate
use.
o
Allow the material to simply evaporate. The pan must
be attended at all times, since vapors of some of
these materials may be somewhat toxic, and no one REFERENCES
should "play" with the material being disposed of.
Continue the evaporation of shallow layers until the The disposal procedures listed in this section are obtained from the
material is gone. following reliable and highly regarded sources:
Lunn , G.; Sansone, E. B. Destruction of Hazardous Chemicals in the
Laboratory, 2nd ed.; John Wiley & Sons: New York, 1984.
Laboratory Waste Disposal Manual; Manufacturing Chemists
Association: Washington, D.C. , 1975.
Armour, M. A., Hazardous Laboratory Chemical Disposal Guide,
Mystery Substances 2nd ed.; Lewis: New York, 1996.
Identify chemical unknowns using Flinn's Hazardous Chemicals, A Manual for Schools and Colleges; Oliver &
Mystery Substance Identification Procedure. Boyd: Edinburgh, 1980.
For a free copy of this valuable procedure, Prudent Practices in the Laboratory; National Academy :
send your request to: Washington, D.C. , 1995.
Flinn Scientific, Inc. Pitt, M. J.; Pitt, E. Handbook of Laboratory Waste Disposal; Ellis
Horwood: Chichester, 1985.
P.O. Box 219 • Batavia, IL 60510
Prudent Practices for Disposal of Chemicals from Laboratories;
National Academy: Washington, D.C., 1983.
FLI"" lCIE"TIFIC I"C. ________"Y4_o_ur_s_a~_er_S_O_UIi_Ce_~_Or_S_CI_·en_C_e_Su_p...pl_ie_s"
BIOLOGICAL WASTE DISPOSAL
Ecological studies have repeatedly demonstrated the intertwined to foster the growth of microorganisms. These organisms will
nature of all elements of the ecosystem. A basic ecological princi- continue to grow even after disposal unless they are destroyed.
ple simply states-"You can't do just one thing ." So when we Contaminating microorganisms may be growing along with known
dispose of materials we are likely to do more than just dispose of the organisms. These organisms must be assumed to be harmful.
materials. When considering the disposal of any material (school or Recent concerns about blood-borne pathogens and body fluid
elsewhere) our goal must be to minimize the environmental impact transmissions have heightened awareness for utilizing sterile tech -
of the disposal, i.e., come as close to doing "one thing " as possi- niques when doing any human physiology experiments or blood
ble. Common sense, a knowledge of the material, and a familiarity typing . For these reasons, all of these laboratory materials must be
with local disposal regulations, procedures and policies must sterilized after use and before disposal.
prevail. The general guidelines provided here are only intended to DISPOSAL PROCEDURES:
stimulate clear thinking about how to minimize our effects on the
Materials that are potentially contaminated with microorganisms
environment as we recycle earth's materials.
must first be sterilized before disposal. After sterilization, they can
One important first step is to formulate a biological waste disposal
usually be disposed of by normal trash removal methods. Check
policy. General guidelines and parameters should be written prior to
with local authorities for rules and regulations that apply to your
conducting actual disposal procedures. Some suggestions that
community. There are two methods for sterilizing wastes: Method
might help in formulating a general biology disposal policy:
IA-autoclaving and Method IB-chemical sterilization.
• Contact your state department of education . Many states have a
science supervisor who might be able to make suggestions on Method IA: Autoclaving
disposal of biohazards or advise you about existing programs Materials can be autoclaved in an autoclave. If an autoclave is not
already in operation . available, a pressure cooker may be used. Biohazard bags should
be used wherever possible and will make the sterilization of some
• If you are located near a large university, biological research facil- biohazard materials easier, while also providing a convenient
ity, hospital, or other biological institution, check with officials for disposal container. Biohazard bags are made of a very durable
possible cooperative activities. You may be able to piggyback plastic that can withstand the high temperature and pressure of
your biohazard materials with their disposal procedures. autoclaving. An indicator patch on the bag turns dark when it has
• You might form a cooperative with other schools in your area been autoclaved/steam processed . The dark patch provides quick
and have a unified disposal plan. There are often savings in bulk external proof that the bag and its contents have been sterilized and
disposal. that it should not be opened .
• Your state equivalent of the Environmental Protection Agency Objects to be autoclaved should be placed into a biohazard bag
(EPA) may have useful resources. carefully without opening the containers (Petri dishes, test tubes,
etc.). Highly dangerous materials should be handled only when
• Your state or national biology teacher associations have resources wearing gloves, masks, and safety eyewear, and practicing other
and guidelines that are very helpful.
sterile precautions. Do not put any sharp objects (blood lancets,
When conducting any disposal procedures, be sure to provide broken glass, dissecting instruments, etc.) into biohazard bags.
personal protection for yourself and others around you . Always The bag should then be tightly sealed by doubling over its end and
wear proper personal protection equipment (goggles, aprons, sealing it shut with a twist tie. Do not overload or "stuff" the bag .
gloves, etc.). Conduct disposal procedures in proper areas for the The bagged biohazard materials should now be autoclaved . The
materials (hoods, ventilated areas, appropriate sinks, etc.). Where bagged biohazard materials should be autoclaved at 15 Ibs. per
appropriate, follow sterile procedures and cautions relative to poten- square inch of pressure for 30 minutes at 121 °C. Follow directions
tial pathogens. for specific autoclaves or pressure cookers very carefully. Use insu-
We have arbitrarily divided waste materials into six categories lated gloves when removing the bags from the autoclaving device.
for the sake of discussion and clarity. Some situations might involve Bags containing glass or other breakable materials should be sepa-
a combination of several of the categories. Specific federal , state, rated from other bags prior to disposal in the trash depending on
and local regulations may apply to the disposal of biohazards from your local practices.
your lab. You must review your obligations and options with regu-
Method IB: Chemical Sterilization
latory and school officials before developing a disposal procedure
at your school. To sterilize, place culture or material in a 10% bleach solution for 24
hours. To prepare 10% bleach solution , dilute one part household
Type I: Potentially harmful due to microorganism -type bleach with nine parts water. Rinse the sterilized materials with
contamination water, and then dispose of them following appropriate procedures.
Type II: Potentially harmful due to dangerous chemical hazards
Type III: Preserved materials
Type IV: Living materials lYpe II POTENTIALLY HARMFUL WASTES DUE
Type V: Sharps and glass items TO DANGEROUS CHEMICAL HAZARDS
Type VI: Common garbage items
EXAMPLES:
Solutions from electrophoresis or staining procedures, formalde-
hyde solutions, or other chemical solutions or solids.
lYpe I POTENTIALLY HARMFUL WASTES
* HAZARDS:
DUE TO MICROORGANISM-TYPE
Chemical wastes may be corrosive, toxic, or flammable and should
CONTAMINATION be handled accordingly. If the waste material is of unknown compo-
sition, assume the material is toxic, corrosive, and flammable and
EXAMPLES: take all precautions when handling the material. Contact Flinn
Bacterial cultures, culture tubes, disposable loops, Petri dishes, Scientific technical staff for advice on how to identify and dispose
blood typing materials, any body fluids, any unknown "growing " of unknown chemical wastes.
items, contaminated media products, disposable gloves used in
DISPOSAL PROCEDURE:
dissections or when handling living materials, electrophoresis mate-
rials, any items which might harbor microorganisms. If the identity of the chemical waste is known, then consult the
chemical waste disposal section of the Flinn Scientific Catalog/
* HAZARDS: Reference Manual. To find the proper disposal procedure, look up
All laboratory wastes that may harbor any microorganisms must be the chemical in the chemical section of the Flinn Scientific Catalog/
assumed to be pathogenic and need to be treated before they are
thrown in the trash. Biological culture media is specifically designed Continued on next page.
1-800-452-1261 Biological Waste Disposal
BIOLOGICAL WASTE DISPOSAL continued state natural resources department. A general disposal procedure
is to wrap the deceased animal in newspaper, place it in a non-
Referen ce Manual , and find the Flinn Suggested Disposal transparent plastic bag, and then throw it in the school's main trash
Procedure (e.g., Disposal : #26a) in the chemical listing. Then find the container if this is allowed. Do not leave the animal where it may be
Flinn Suggested Disposal Procedure in the Chemical Disposal discovered by students.
Procedures section of the reference manual. The disposal of chem- Microorganism cultures, such as protozoans, should be steril-
ical wastes is regulated by federal , state, and local ordinances; do ized by Method IA or 18 as outlined earlier and then flushed down
not perform any disposal procedure without first consulting with the drain.
your local government regulatory officials. Very small dead fish can be simply flushed down the drain if the
school is hooked up to a municipal water treatment facility.