An isomerization method consists of a deisobutanizer column receives feed comprising n-butane. The deisobutanizer column delivers its bottoms a portion to a reboiler and another portion along with hydrogen is routed to a isomerization reactor and the reactor effluent is returned to the column. A stabilizer which is integrated with the column, an overhead stream used as a reflux and bottoms containing an iso-butane-rich stream that is the iso-butane product stream.

The column overhead effluent is routed to separator, which splits the hydrocarbons and effluent, where the hydrocarbons are routed to deisobutanizer column and effluent recycled to stabilizer, where the stabilizer separates the reactor effluent into product streams contains an iso-butane product stream, a n-butane product stream, and a lighter hydrocarbon product stream.

The present disclosure relates generally to processes and apparatuses for separating an effluent in an acetic acid production unit. Accordingly, one aspect of the disclosure provides a process including introducing a feed stream comprising acetic acid and water into a distillation column through a feed inlet, separating the feed stream to form a water-rich first fraction and an acetic acid-rich second fraction, measuring an internal temperature and an internal pressure of the column at positions between a first outlet and a second outlet of the column, determining a corrected temperature of the column based on the measured internal pressure and internal temperature of the column, adjusting a heating rate of a heat source in thermal communication with a bottom section of the column if the corrected temperature differs from a target value, and then withdrawing at least a portion of the separated acetic acid-rich second fraction, the fraction comprising 500-1,500 ppm water by weight (ppmw).

The present disclosure relates generally to processes and apparatuses for separating an effluent in an acetic acid production unit. Accordingly, one aspect of the disclosure provides a process including introducing a feed stream comprising acetic acid and water into a distillation column through a feed inlet, separating the feed stream to form a water-rich first fraction and an acetic acid-rich second fraction, measuring an internal temperature and an internal pressure of the column at positions between a first outlet and a second outlet of the column, determining a corrected temperature of the column based on the measured internal pressure and internal temperature of the column, adjusting a heating rate of a heat source in thermal communication with a bottom section of the column if the corrected temperature differs from a target value, and then withdrawing at least a portion of the separated acetic acid-rich second fraction, the fraction comprising 500-1,500 ppm water by weight (ppmw).

Producing C5 olefins from steam cracker C5 feeds may include reacting a mixed hydrocarbon stream comprising cyclopentadiene, C5 olefins, and C6+ hydrocarbons in a dimerization reactor where cyclopentadiene is dimerized to dicyclopentadiene. The dimerization reactor effluent may be separated into a fraction comprising the C6+ hydrocarbons and dicyclopentadiene and a second fraction comprising C5 olefins and C5 dienes. The second fraction, a saturated hydrocarbon diluent stream, and hydrogen may be fed to a catalytic distillation reactor system for concurrently separating linear C5 olefins from saturated hydrocarbon diluent, cyclic C5 olefins, and C5 dienes contained in the second fraction and selectively hydrogenating C5 dienes. An overhead distillate including the linear C5 olefins and a bottoms product including cyclic C5 olefins are recovered from the catalytic distillation reactor system. Other aspects of the C5 olefin systems and processes, including catalyst configurations and control schemes, are also described.

Producing C5 olefins from steam cracker C5 feeds may include reacting a mixed hydrocarbon stream comprising cyclopentadiene, C5 olefins, and C6+ hydrocarbons in a dimerization reactor where cyclopentadiene is dimerized to dicyclopentadiene. The dimerization reactor effluent may be separated into a fraction comprising the C6+ hydrocarbons and dicyclopentadiene and a second fraction comprising C5 olefins and C5 dienes. The second fraction, a saturated hydrocarbon diluent stream, and hydrogen may be fed to a catalytic distillation reactor system for concurrently separating linear C5 olefins from saturated hydrocarbon diluent, cyclic C5 olefins, and C5 dienes contained in the second fraction and selectively hydrogenating C5 dienes. An overhead distillate including the linear C5 olefins and a bottoms product including cyclic C5 olefins are recovered from the catalytic distillation reactor system. Other aspects of the C5 olefin systems and processes, including catalyst configurations and control schemes, are also described.

Producing C5 olefins from steam cracker C5 feeds may include reacting a mixed hydrocarbon stream comprising cyclopentadiene, C5 olefins, and C6+ hydrocarbons in a dimerization reactor where cyclopentadiene is dimerized to dicyclopentadiene. The dimerization reactor effluent may be separated into a fraction comprising the C6+ hydrocarbons and dicyclopentadiene and a second fraction comprising C5 olefins and C5 dienes. The second fraction, a saturated hydrocarbon diluent stream, and hydrogen may be fed to a catalytic distillation reactor system for concurrently separating linear C5 olefins from saturated hydrocarbon diluent, cyclic C5 olefins, and C5 dienes contained in the second fraction and selectively hydrogenating C5 dienes. An overhead distillate including the linear C5 olefins and a bottoms product including cyclic C5 olefins are recovered from the catalytic distillation reactor system. Other aspects of the C5 olefin systems and processes, including catalyst configurations and control schemes, are also described.

The invention relates to a process for the preparation of styrene or substituted styrenes comprising the steps of: (a) subjecting a feed containing 1-phenyl ethanol or substituted 1-phenyl ethanol to a dehydration treatment in the presence of a suitable dehydration catalyst; (b) subjecting the resulting product mixture to a separation treatment, thus obtaining a stream containing water and styrene or substituted styrene and a residual fraction containing heavy ends; (c) treating the stream containing water and styrene or substituted styrene with a base; (d) separating the treated stream of step (c) into a styrene or substituted styrene-rich product stream and a styrene or substituted styrene-lean waste water stream; (e) treating the styrene or substituted styrene-lean waste water stream with steam in a stripping column, thus obtaining a treated waste water stream and a treated stream comprising steam and styrene or substituted styrene.

The invention relates to a process for the preparation of styrene or substituted styrenes comprising the steps of: (a) subjecting a feed containing 1-phenyl ethanol or substituted 1-phenyl ethanol to a dehydration treatment in the presence of a suitable dehydration catalyst; (b) subjecting the resulting product mixture to a separation treatment, thus obtaining a stream containing water and styrene or substituted styrene and a residual fraction containing heavy ends; (c) treating the stream containing water and styrene or substituted styrene with a base; (d) separating the treated stream of step (c) into a styrene or substituted styrene-rich product stream and a styrene or substituted styrene-lean waste water stream; (e) treating the styrene or substituted styrene-lean waste water stream with steam in a stripping column, thus obtaining a treated waste water stream and a treated stream comprising steam and styrene or substituted styrene.

The invention relates to a process for the preparation of styrene or substituted styrenes comprising the steps of: (a) subjecting a feed containing 1-phenyl ethanol or substituted 1-phenyl ethanol to a dehydration treatment in the presence of a suitable dehydration catalyst; (b) subjecting the resulting product mixture to a separation treatment, thus obtaining a stream containing water and styrene or substituted styrene and a residual fraction containing heavy ends; (c) treating the stream containing water and styrene or substituted styrene with a base; (d) separating the treated stream of step (c) into a styrene or substituted styrene-rich product stream and a styrene or substituted styrene-lean waste water stream; (e) treating the styrene or substituted styrene-lean waste water stream with steam in a stripping column, thus obtaining a treated waste water stream and a treated stream comprising steam and styrene or substituted styrene.

Producing C5 olefins from steam cracker C5 reeds may include reacting a mixed hydrocarbon stream comprising cyclopentadiene, C5 olefins, and C6+ hydrocarbons in a dimerization reactor where cyclopentadiene is dimerized to dicyclopentadiene. The dimerization reactor effluent may be separated into a traction comprising the C6+ hydrocarbons and dicyclopentadiene and a second fraction comprising C5 olefins and C5 dienes. The second fraction, a saturated hydrocarbon diluent stream, and hydrogen may be fed to a catalytic distillation reactor system for concurrently separating linear C5 olefins from saturated hydrocarbon diluent, cyclic C5 olefins, and C5 dienes contained in the second fraction and selectively hydrogenating C5 dienes. An overhead distillate including the linear C5 olefins and a bottoms product including cyclic C5 olefins are recovered from the catalytic distillation reactor system. Other aspects of the C5 olefin systems and processes, including catalyst configurations and control schemes, are also described.