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Diisopropyl sulfite

Apart from the conversion of peroxides to useful products, it is sometimes necessary to reduce peroxides, and especially hydroperoxides formed by auto-oxidation. Such compounds are formed especially in hydrocarbons containing branched chains, double bonds or aromatic rings, and in ethers such as diethyl ether, diisopropyl ether, tetrahydrofuran, dioxane, etc. Since most peroxidic compounds decompose violently at higher temperatures and could cause explosion and fire it is necessary to remove them from liquids they contaminate. Water-immiscible liquids can be stripped of peroxides by shaking with an aqueous solution of sodium sulfite or ferrous sulfate. A simple and efficient way of removing peroxides is treatment of the contaminated compounds with 0.4 nm molecular sieves [669]. [Pg.85]


See other pages where Diisopropyl sulfite is mentioned: [Pg.319]    [Pg.184]    [Pg.615]    [Pg.319]    [Pg.184]    [Pg.615]    [Pg.1106]    [Pg.508]    [Pg.378]    [Pg.513]    [Pg.135]    [Pg.37]   
See also in sourсe #XX -- [ Pg.147 ]




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