Lummus Technology Inc.

Catalytic Distillation Technologies

Martinus Johannes Almering

Willibrord A Groten

Rosette Barias

Montri Vichailak

Purvis K Ho

Lawrence A Smith, Jr

Gary G Podrebarac

Mitchell E Loescher

Michael Jon Scott

Romain Lemoine

Yongqiang Xu

Arvids Judzis, Jr

Manoj Som

Kerman Dukandar

Christopher Robbins

Todd Vogt

Oliver Chen

A process and system for converting bio ethanol to high purity isobutene is provided. The system includes a dehydration unit configured to receive a bio ethanol containing stream, convert the bio ethanol to bio ethylene, and produce a bio ethylene containing stream, a dimerization unit configured to receive the bio ethylene stream, dimerize ethylene, and produce an n-butenes containing stream, a skeletal isomerization unit configured to receive the n-butenes containing stream, convert n-butenes to produce a skeletal isomerization stream comprising an isobutene, isobutane, n-butenes, and n-butane, and a catalytic separation unit configured to receive the skeletal isomerization stream, convert olefins and/or isoolefins contained therein to produce a converted skeletal isomerization reaction product, and to fractionate the skeletal isomerization reaction product and produce bio isobutene.

Process for the efficient production of bio high purity isobutene from renewables

A process for converting isobutane to propylene. The process including dehydrogenating isobutane to produce a mixed product stream comprising isobutane and isobutene, skeletal isomerizing the mixed product stream comprising isobutane and isobutene to convert isobutene to n-butenes including 1-butene and 2-butenes and to recover a skeletal isomerization reaction product comprising isobutane, isobutene, butadiene, 1-butene, and 2-butenes. The process further including fractionating the skeletal isomerization reaction product, isomerizing the 1-butene contained therein to 2-butenes, recovering an overhead fraction comprising isobutane, a side draw fraction comprising isobutane and isobutene, and a bottoms fraction comprising 2-butenes, and combining the bottoms fraction with ethylene and converting the ethylene and 2-butenes to produce a reaction effluent comprising propylene.

Converting isobutane and refinery C4S to propylene

Systems and processes disclosed may be used to produce a high purity isobutane stream and a high purity 1-butene stream from mixed C4 streams having disparate starting compositions.

Co-production of high purity isobutane and butene-1 from mixed C4s

Processes for the production of high purity isobutylene are disclosed. The processes may include supplying a mixed C4 feed stream to a catalytic distillation column, which may contain a butene isomerization catalyst. 1-butene is isomerized to 2-butene and concurrently in the catalytic distillation column the 2-butene is separated from the isobutane and isobutylene. The overheads fraction comprising the isobutane and isobutylene is then condensed in an overheads system and fed to a splitter, where the isobutane is separated from the isobutylene. The process further includes operating the catalytic distillation column at an overheads temperature greater than a bottoms temperature of the splitter, and heating a portion of the splitter bottoms stream via indirect heat exchange with at least a portion of the catalytic distillation column overheads fraction, thereby producing a heated bottoms stream (reboil vapor) fed to the splitter and a cooled overheads fraction.

Process for the production of high purity isobutylene

A process for reducing the concentration of benzene in a hydrocarbon stream, the process including: fractionating a reformate to form a benzene concentrate fraction comprising benzene and other Chydrocarbons, and a heavies fraction comprising Chydrocarbons; and hydrogenating the benzene concentrate fraction to form a hydrocarbon fraction having a reduced benzene concentration.

Process for ultra low benzene reformate using catalytic distillation

A process for recovering benzene, the process including: feeding hydrogen and a hydrocarbon fraction comprising benzene, components lighter than benzene, components heavier than benzene, and diolefins to a catalytic distillation reactor system comprising at least one reaction zone comprising a hydrogenation catalyst; concurrently in the catalytic distillation reactor system: contacting the diolefins and hydrogen in the presence of the hydrogenation catalyst to selectively hydrogenate at least a portion of the diolefins; and fractionating the hydrocarbon fraction to form a fraction comprising benzene and other Chydrocarbons, and a heavies fraction comprising Chydrocarbons; recovering the heavies fraction from the first catalytic distillation reactor system as a bottoms fraction; and withdrawing the fraction comprising benzene and other Chydrocarbons from the catalytic distillation reactor system as a benzene concentrate fraction.

Use of catalytic distillation for benzene separation and purification

A process for fractionating isobutene from normal butenes, including: introducing hydrogen and a feed stream comprising isobutene, 1-butene, and 2-butene into a first column including a reaction zone containing a hydroisomerization catalyst operating at a first pressure and concurrently: (i) converting at least a portion of the 1-butene to 2-butene, and (ii) separating isobutene from the 2-butene; recovering a first overheads fraction comprising isobutene from the first column; recovering a first bottoms fraction comprising isobutene, 2-butene, and unreacted 1-butene from the first column; introducing the first bottoms fraction into a top portion of a second column comprising a fractionation column operating at a second pressure lower than the first pressure; separating the first bottoms into a second overheads fraction comprising isobutene and 1-butene and a second bottoms fraction comprising 2-butene; compressing the second overheads fraction; and introducing the compressed second overheads fraction to a lower portion of the first column.

Deisobutenizer

A light cracked naphtha is treated to convert mercaptans to sulfides and saturate dienes and then subjected to destructive hydrodesulfurization (HDS) to convert the organic sulfur compounds to hydrogen sulfide. The recombinant mercaptans formed by reaction of hydrogen sulfide and olefins at the outlet of the HDS are generally heavier than the light cracked naphtha is fractionated in admixture with a heavy cracked naphtha. A low sulfur content light cracked naphtha is produced as an overheads and the major portion of the mercaptans leave with heavy cracked naphtha as bottoms. It also advantageous to pass the heavy cracked naphtha through the HDS in admixture with the light cracked naphtha, since the recombinant mercaptans formed with the heavy cracked naphtha olefins (which displace some of the lower mercaptans which would form the light cracked naphtha olefins) will be even higher boiling and easier to separate by fractionation.

Growing community of inventors

Houston, TX, United States of America

Martinus Johannes Almering