C - Chemistry – Metallurgy – 07 – D
Patent
C - Chemistry, Metallurgy
07
D
C07D 303/04 (2006.01) C07C 29/132 (2006.01) C07C 29/48 (2006.01) C07C 31/02 (2006.01) C07D 301/19 (2006.01)
Patent
CA 2101006
EPOXIDATION PROCESS FOR MANUFACTURE OF OLEFIN OXIDE AND ALCOHOL ABSTRACT An epoxidation reaction wherein: an olefin and an organic hydroperoxide, preferably, propylene and tertiary butyl hydroperoxide are reacted in a primary reaction zone in a liquid phase with an organic solvent, preferably tertiary butyl alcohol, in the presence of a soluble molybdenum catalyst at a ratio of propylene to tertiary butyl hydroperoxide of from about 0.9:1 to about 3:1, at a reaction temperature from about 100°C to about 140°C and a residence time sufficient to convert about 85 to 95% of the tertiary butyl hydroperoxide and form a primary epoxidation zone reaction product; fractionating, in a primary fractionation zone, the primary zone reaction product into a primary distillate fraction comprising unreacted propylene and propylene oxide and into a primary heavy liquid fraction, comprising molybdenum catalyst, unreacted tertiary butyl hydroperoxide, tertiary butyl alcohol and side reaction products; reactin, in a secondary epoxidation reaction zone, the primary heavy liquid fraction with propylene in the liquid phase, with substantially no back mixing, at a molar ratio of propylene to unreacted tertiary butyl hydroperoxide of about 5:1 to about 10:1, a reaction temperature of about 110°C to about 140°C and a residence time sufficient for conversion of substantially all the tertiary butyl hydroperoxide and production of a secondary reaction zone product; fractionating the secondary reaction zone product, in a secondary distillation zone, into a secondary distillate fraction comprising unreacted propylene, and propylene oxide, and into a secondary heavy liquid fraction comprising molybdenum catalyst, tertiary butyl alcohol, and side reaction products; recovering the secondary heavy liquid product for recovery and/or disposal of molybdenum; and fractional distillation of the first distillate fraction and the second distillate fraction for recovery of propylene, and propylene oxide product.
Keating Kenneth Patrick
Marquis Edward Thomas
Mueller Mark Allan
Huntsman Specialty Chemicals Corporation
Smart & Biggar
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