The present invention relates to an intensification of the synthetic process for the preparation of dialkyl ether from alcohol by using a conical fixed bed reactor integrated with distillation coupled conical polishing reactor.

The present invention relates to an intensification of the synthetic process for the preparation of dialkyl ether from alcohol by using a conical fixed bed reactor integrated with distillation coupled conical polishing reactor.

A process for the selective dimerization and etherification of isoolefins, including feeding a mixed C4 stream and an oxygenate stream to a first fixed bed reactor containing a first catalyst, producing a first reactor effluent comprising dimers of the isoolefin, unreacted C4s, and unreacted oxygenates. Feeding the first reactor effluent directly to a second fixed bed reactor containing a second catalyst, producing a second reactor effluent containing dimers of the isoolefin, unreacted C4s, and unreacted oxygenates. Feeding the second reactor effluent to a catalytic distillation reactor system containing a third catalyst. Concurrently in the catalyst distillation reactor system reacting unreacted C4s in the presence of the third catalyst to form additional dimers of the isoolefin and/or ethers, and separating the dimers of the isoolefins from unreacted oxygenates and unreacted C4s.

A process for the selective dimerization and etherification of isoolefins, including feeding a mixed C4 stream and an oxygenate stream to a first fixed bed reactor containing a first catalyst, producing a first reactor effluent comprising dimers of the isoolefin, unreacted C4s, and unreacted oxygenates. Feeding the first reactor effluent directly to a second fixed bed reactor containing a second catalyst, producing a second reactor effluent containing dimers of the isoolefin, unreacted C4s, and unreacted oxygenates. Feeding the second reactor effluent to a catalytic distillation reactor system containing a third catalyst. Concurrently in the catalyst distillation reactor system reacting unreacted C4s in the presence of the third catalyst to form additional dimers of the isoolefin and/or ethers, and separating the dimers of the isoolefins from unreacted oxygenates and unreacted C4s.

The invention relates to a new industrial process for manufacturing of perfluoro(methylvinylether) (PFMVE), and of 2-fluoro-1,2-dichloro-trifluoro-methoxyethylene (FCTFE), involving reactions in liquid phase and performing reactions in a microreactor. The invention also relates to a new industrial process for manufacturing of perfluoro(methyl vinyl ether) (PFMVE) by fluorination, i.e., perfluorination, of 2-fluoro-1,2-dichloro-trifluoromethoxy-ethylene (FCTFE) with HF (hydrogen fluoride) in the presence of a Lewis acid catalyst, again performing the reaction in liquid phase, and preferably in a microreactor.

The invention relates to a new industrial process for manufacturing of perfluoro(methylvinylether) (PFMVE), and of 2-fluoro-1,2-dichloro-trifluoro-methoxyethylene (FCTFE), involving reactions in liquid phase and performing reactions in a microreactor. The invention also relates to a new industrial process for manufacturing of perfluoro(methyl vinyl ether) (PFMVE) by fluorination, i.e., perfluorination, of 2-fluoro-1,2-dichloro-trifluoromethoxy-ethylene (FCTFE) with HF (hydrogen fluoride) in the presence of a Lewis acid catalyst, again performing the reaction in liquid phase, and preferably in a microreactor.

Systems and methods for producing MTBE without using a catalytic distillation column or a super fractionator have been disclosed. An optimum volume of methanol stream required to maximize MTBE production and reduce slippage of isobutylene to minimum acceptable values together with a crude C4 stream are flowed into a primary reaction unit that comprises a first reactor and a second reactor in parallel configured to produce maximum values of final MTBE volumes under higher or equal established purity commercial quality specifications levels. The combined effluent from the first reactor and the second reactor is split to form a first portion, a second portion and a third portion. The first portion is flowed to a third reactor configured to produce additional MTBE. The second portion is combined with an effluent from the third reactor for further separation. The third portion is recycled to the first reactor and/or second reactor.

Systems and methods for producing MTBE without using a catalytic distillation column or a super fractionator have been disclosed. An optimum volume of methanol stream required to maximize MTBE production and reduce slippage of isobutylene to minimum acceptable values together with a crude C4 stream are flowed into a primary reaction unit that comprises a first reactor and a second reactor in parallel configured to produce maximum values of final MTBE volumes under higher or equal established purity commercial quality specifications levels. The combined effluent from the first reactor and the second reactor is split to form a first portion, a second portion and a third portion. The first portion is flowed to a third reactor configured to produce additional MTBE. The second portion is combined with an effluent from the third reactor for further separation. The third portion is recycled to the first reactor and/or second reactor.

The present invention relates to a process for separating 1-methoxypropan-2-ol in a stream S3 from an aqueous stream comprising 1-methoxypropan-2-ol and 2-methoxypropan-1-ol, wherein the process comprises providing a stream S0 comprising 1-methoxypropan-2-ol, 2-methoxypro-pan-1-ol and water, and having a molar ratio of 1-methoxypropan-2-ol:2-methoxypropan-1-ol in the range of from 1:5 to 5:1. A further aspect of the invention also relates to 1-methoxypropan-2-ol obtained or obtainable from said process, as well as to a mixture of 1-methoxypropan-2-ol and 2-methoxypropan-1-ol, preferably obtained or obtainable from said process, which preferably comprises in the range of from 95 to 100 weight-% 1-methoxypropan-2-ol and ≤0.5 weight-% of 2-methoxypropan-1-ol, each based on the total weight of the mixture.

The present invention relates to a process for separating 1-methoxypropan-2-ol in a stream S3 from an aqueous stream comprising 1-methoxypropan-2-ol and 2-methoxypropan-1-ol, wherein the process comprises providing a stream S0 comprising 1-methoxypropan-2-ol, 2-methoxypro-pan-1-ol and water, and having a molar ratio of 1-methoxypropan-2-ol:2-methoxypropan-1-ol in the range of from 1:5 to 5:1. A further aspect of the invention also relates to 1-methoxypropan-2-ol obtained or obtainable from said process, as well as to a mixture of 1-methoxypropan-2-ol and 2-methoxypropan-1-ol, preferably obtained or obtainable from said process, which preferably comprises in the range of from 95 to 100 weight-% 1-methoxypropan-2-ol and ≤0.5 weight-% of 2-methoxypropan-1-ol, each based on the total weight of the mixture.