Patent classifications
C07C41/05
PROCESS FOR PRODUCING DIMETHYL ETHER (DME) FROM SYNTHESIS GAS
The invention relates to a process for producing dimethyl ether (DME). The invention provides that a first and a second reaction zone in which catalyst fills are arranged between two adjacent pillow plates and are traversable by the respective input gas are arranged in a common synthesis reactor. The pillow plates are traversable by a fluid cooling medium. The DME-containing product gas stream exiting the synthesis reactor is resolved into a DME end product stream, a gas byproduct stream containing unconverted carbon oxides and hydrogen, a methanol byproduct stream and a wastewater stream. The gas byproduct stream is at least partially returned to the reactor inflow to increase the altogether achieved DME yield.
Dimerization and trimerization of C5 olefins via catalytic distillation
A process for the selective dimerization and etherification of isoolefins. The process including feeding a mixed C5 stream to a selective hydrogenation unit to convert dienes to olefins and isoolefins, producing a hydrogenated effluent stream. The hydrogenated effluent stream is fed to a first fixed bed reactor, producing a first reactor effluent. The first reactor effluent is fed to a catalytic distillation reactor system, producing a first overheads including unreacted olefins, isoolefins, oxygenate, and one or more C5 ethers and a first bottoms including dimers of the isoolefins, any produced trimers of the isoolefins, and heavy oxygenates. The first overheads is fed to a second fixed bed reactor, producing a second reactor effluent including dimers of the isoolefins, unreacted C5s, and unreacted oxygenates. The first bottoms stream and the second reactor effluent are combined and fed to a product splitter, producing a second overheads stream including unreacted C5 olefins, isoolefins, and oxygenates and a second bottoms stream including C10+ hydrocarbons.
Dimerization and trimerization of C5 olefins via catalytic distillation
A process for the selective dimerization and etherification of isoolefins. The process including feeding a mixed C5 stream to a selective hydrogenation unit to convert dienes to olefins and isoolefins, producing a hydrogenated effluent stream. The hydrogenated effluent stream is fed to a first fixed bed reactor, producing a first reactor effluent. The first reactor effluent is fed to a catalytic distillation reactor system, producing a first overheads including unreacted olefins, isoolefins, oxygenate, and one or more C5 ethers and a first bottoms including dimers of the isoolefins, any produced trimers of the isoolefins, and heavy oxygenates. The first overheads is fed to a second fixed bed reactor, producing a second reactor effluent including dimers of the isoolefins, unreacted C5s, and unreacted oxygenates. The first bottoms stream and the second reactor effluent are combined and fed to a product splitter, producing a second overheads stream including unreacted C5 olefins, isoolefins, and oxygenates and a second bottoms stream including C10+ hydrocarbons.
Etherification of high concentration C5 ISO-olefins via catalytic distillation
Systems and processes for the efficient conversion of high concentration isoolefin streams to tertiary alkyl ethers are disclosed. The systems and processes may include a feed system to advantageously divide the high concentration isoolefin feed to multiple fixed bed reactors and a catalytic distillation reactor to control the reaction exotherm and achieve a high isoolefin conversion.
Etherification of high concentration C5 ISO-olefins via catalytic distillation
Systems and processes for the efficient conversion of high concentration isoolefin streams to tertiary alkyl ethers are disclosed. The systems and processes may include a feed system to advantageously divide the high concentration isoolefin feed to multiple fixed bed reactors and a catalytic distillation reactor to control the reaction exotherm and achieve a high isoolefin conversion.
ETHERIFICATION OF HIGH CONCENTRATION C5 ISO-OLEFINS VIA CATALYTIC DISTILLATION
Systems and processes for the efficient conversion of high concentration isoolefin streams to tertiary alkyl ethers are disclosed. The systems and processes may include a feed system to advantageously divide the high concentration isoolefin feed to multiple fixed bed reactors and a catalytic distillation reactor to control the reaction exotherm and achieve a high isoolefin conversion.
Process for the preparation of N-iodoamides
The present invention provides new stable crystalline N-iodoamides-1-iodo-3,5,5-trimethylhydantoin (1-ITMH) and 3-iodo-4,4-dimethyl-2-oxazolidinone (IDMO). The present invention further provides a process for the preparation of organic iodides using N-iodoamides of this invention and recovery of the amide co-products from waste water.
Process for the preparation of N-iodoamides
The present invention provides new stable crystalline N-iodoamides-1-iodo-3,5,5-trimethylhydantoin (1-ITMH) and 3-iodo-4,4-dimethyl-2-oxazolidinone (IDMO). The present invention further provides a process for the preparation of organic iodides using N-iodoamides of this invention and recovery of the amide co-products from waste water.
Process for the preparation of N-iodoamides
The present invention provides new stable crystalline N-iodoamides-1-iodo-3,5,5-trimethylhydantoin (1-ITMH) and 3-iodo-4,4-dimethyl-2-oxazolidinone (IDMO). The present invention further provides a process for the preparation of organic iodides using N-iodoamides of this invention and recovery of the amide co-products from waste water.
Olefin conversion process
A process for the production of C.sub.4 olefins, which may include: contacting a hydrocarbon mixture comprising alpha-pentenes with an isomerization catalyst to form an isomerization product comprising beta-pentenes; contacting ethylene and the beta-pentenes with a first metathesis catalyst to form a first metathesis product comprising butenes and propylene, as well as any unreacted ethylene and C.sub.5 olefins; and fractionating the first metathesis product to for an ethylene fraction, a propylene fraction, a butene fraction, and a C.sub.5 fraction.