APPENDIX 4
PEROXIDIZABLE COMPOUNDS
Some ethers and conjugated olefins may form explosive
peroxides during storage especially after opening of the container. This can pose a danger when these solvents
are distilled. Compounds listed below
are readily peroxidizable under normal storage
conditions.
Aldehydes and amides, although easily peroxidized, are
NOT known to accumulate peroxides to dangerous levels. Peroxidation hazards fall into three
categories: A) those compounds which form explosive compounds without
concentration, B) those compounds forming dangerous peroxides only upon
concentration, C) monomers in which peroxides may initiate explosive
polymerization. A few representative
examples are listed below:
A B C
Isopropyl ether Diethyl
ether Methyl
methacrylate
Divinyl acetylene Tetrahydrofuran Styrene
Vinylidene chloride Dioxane Acrylic acid
Potassium metal Dicyclopentadiene Acrylonitrile
Sodium amide Decalin
Butadiene
Tetralin
Tetrafluoroethylene
Cyclohexene Chloroprene
Diglyme
Vinyl
compounds
All
peroxidizable compounds should be stored away from heat and light. A nitrogen atmosphere is preferred except in
the case of some inhibited vinyl monomers.
Peroxidizable solvents should always be treated as though they contain
peroxides. Compounds in category A
should be evaluated for peroxides at least every three months. A small portion of the compound should be
tested with moist starch‑iodide paper:
the slightest blue coloration indicates the presence of peroxides. Compounds in category B should not be stored
for more than 12 months after opening unless shown by testing to be free of
peroxides. If these materials are to be
retained after a positive test, they must be treated to remove peroxides,
rebottled and the label redated.
Uninhibited vinyl monomers (category C) should not be stored for more
than 24 hours. Small quantities
(<10g) containing a suitable inhibitor may be stored for longer than 24
hours only with discretion. Inhibited
vinyl monomers should be stored under air rather than nitrogen.
All peroxidizable compounds should bear a proper warning
label containing the date of receipt and
the date on which the container was first opened. The inventory should be reviewed every three months and proper
testing and disposal carried out.
Before distilling peroxidizable compounds, they should be checked for
peroxides and at least 10% of the volume should be left undistilled.
The following are possible methods for removing peroxides
from solvents (J. Chem. Ed. 47,
A175, 1970). Method 2 has the
disadvantage of wetting the solvent and may leave traces of decomposition
products in the solvent. Method 1. A convenient method is to pass the solvent through a short column
of alumina. This may in some cases
leave some peroxides unchanged on the column.
The alumina should therefore be added to a dilute acidic solution of
potassium iodide or ferrous sulfate before disposal. Method 2. Water insoluble solvents may be shaken with
a concentrated solution of ferrous salt (60g of ferrous sulfate and 6mL of
conc. sulfuric acid in 110 mL of water).
Traces of aldehydes may be produced and the solvent will be left
wet. For greater purity, the solvent
should be shaken with 0.5% potassium permanganate followed by 5% NaOH and
water.