Propylene oxide

Propylene oxide is similar in its structure to ethylene oxide, but due to the presence of an additional methyl group, it has different physical and chemical properties. It is a liquid that boils at 33.9°C, and it is only slightly soluble in water. (Ethylene oxide, a gas, is very soluble in water).

The main method to obtain propylene oxide is chlorohydrination followed by epoxidation. This older method still holds a dominant role in propylene oxide production. Chlorohydrination is the reaction between an olefin and hypochlorous acid. When propylene is the reactant, propylene chlorohydrin is produced. The reaction occurs at approximately 35°C and normal pressure without any catalyst:

Approximately 87–90% yield could be achieved. The main by-product is propylene dichloride (6–9%). The next step is the dehydrochlorination of the chlorohydrin with a 5% Ca(OH)₂ solution:

Propylene oxide is purified by steam stripping and then distillation. Byproduct propylene dichloride may be purified for use as a solvent or as a feed to the perchloroethylene process. The main disadvantage of the chlorohydrination process is the waste disposal of CaCl₂. Figure 1.1 is a flow diagram of a typical chlorohydrin process.  The second important process for propylene oxide is epoxidation with peroxides. Many hydroperoxides have been used as oxygen carriers for this reaction. Examples are t-butylhydroperoxide, ethylbenzene hydroperoxide, and peracetic acid. An important advantage of the process is that the coproducts from epoxidation have appreciable economic values. Epoxidation of propylene with ethylbenzene hydroperoxide is carried out at approximately 130°C and 35 atmospheres in presence of molybdenum catalyst. A conversion of 98% on the hydroperoxide has been reported:

The coproduct α-phenylethyl alcohol could be dehydrated to styrene. Ethylbenzene hydroperoxide is produced by the uncatalyzed reaction of ethylbenzene with oxygen:

Figure 1.1. A flow diagram of a typical chlorohydrin process for producing propylene oxide.

Table 1.1 shows those peroxides normally used for epoxidation of propylene and the coproducts with economic value.

Epoxidation with hydrogen peroxide has also been tried. The epoxidation reaction is catalyzed with compounds of As, Mo, and B, which are claimed to produce propylene oxide in high yield:

Table 1.1: Peroxides actually or potentially used to epoxidize propylene

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