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US4062903A Expired / Lapsed US ⏱️ 0.0 years remaining

Process for isomerizing alkylaromatics

Assignee: Chevron USA Inc
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Filing: 1976-09-24
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Granted: 1977-12-13
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Expires: 1996-09-24
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Abstract

Abstract A process is disclosed for producing a selected C 8 alkylaromatic isomer from a feedstock containing a less than equilibrium concentration of the selected isomer and a low C 8 naphthenes concentration, in which the feedstock is first contacted with a platinum-halogen catalyst at low temperature isomerization conditions to form an intermediate reaction mixture containing a substantial amount of C 8 naphthenes and a partially isomerized mixture of C 8 alkylaromatics; the intermediate mixture is then contacted with another platinum-halogen catalyst at higher temperature dehydrogenation conditions to form a final product mixture with a very low naphthenes content and a substantially equilibrium concentration of the selected isomer; and the selected xylene isomer is recovered from the final product mixture.

Inventors

  • 👤 Robert L. Jacobson

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-08 10:17
CPC Classifications
C; C07; C07C; C07C15/00; C07C15/02; C07C15/067; C07C15/08; C07C5/00; C07C5/02; C07C5/13; C07C5/32; C07C5/367; C07C2521/00; C07C2521/02; C07C2521/04; C07C2523/00; C07C2523/16; C07C2523/32; C07C2523/36; C07C2523/38; C07C2523/40; C07C2523/42; C07C2523/54; C07C2523/56; C07C2523/64; C07C2523/656; Y; Y02; Y02P; Y02P20/00; Y02P20/50; Y02P20/52

Claims Analysis

Total Claims: 4
Claim 1
Independent Claim 249 words
A process for producing a first selected xylene isomer from a feedstock including a substantially greater than equilibrium concentration of ethylbenzene, a substantially less than equilibrium concentration of said selected isomer, and a weight ratio of C 8 naphthenes to C 8 alkylaromatics of less than 1:50, comprising the steps of: a. forming an intermediate reaction mixture having a weight ratio of C 8 naphthenes to C 8 alkylaromatics of greater than 1:50 and less than 1:10 by contacting said feedstock and hydrogen with a first catalyst comprising 0.1-3 weight percent platinum, 0.1-3 weight percent rhenium and 1.25-2.0 weight percent chloride on an alumina carrier at isomerization conditions including an isomerization temperature between about 750° F and 900° F and an isomerization hydrogen pressure of about 100 psia to 250 psia; b. forming a final hydrocarbon product mixture including a substantially equilibrium concentration of said first isomer and having a weight ratio of C 8 naphthenes to C 8 alkylaromatics of less than 1:50 by contacting said intermediate reaction mixture with a second catalyst having essentially the same composition as said first catalyst and comprising 0.1-3 weight percent platinum, 0.1-3 weight percent rhenium, and 1.25-2.0 weight percent chloride on an alumina carrier at dehydrogenation conditions including a temperature at least 25° F above said isomerization hydrogen temperature and in the range from about 775° F to 950° F and a pressure not higher than said isomerization hydrogen pressure; and c. recovering said first isomer from said final product mixture.
Claim 2
Dependent Claim 249 words
A process for producing a first selected xylene isomer from a feedstock including a substantially greater than equilibrium concentration of ethylbenzene, a substantially less than equilibrium concentration of said selected isomer, and a weight ratio of C 8 naphthenes to C 8 alkylaromatics of less than 1:50, comprising the steps of: a. forming an intermediate reaction mixture having a weight ratio of C 8 naphthenes to C 8 alkylaromatics of greater than 1:50 and less than 1:10 by contacting said feedstock and hydrogen with a first catalyst comprising 0.1-3 weight percent platinum, 0.1-3 weight percent rhenium and 1.25-2.0 weight percent chloride on an alumina carrier at isomerization conditions including an isomerization temperature between about 750° F and 900° F and an isomerization hydrogen pressure of about 100 psia to 250 psia; b. forming a final hydrocarbon product mixture including a substantially equilibrium concentration of said first isomer and having a weight ratio of C 8 naphthenes to C 8 alkylaromatics of less than 1:50 by contacting said intermediate reaction mixture with a second catalyst having essentially the same composition as said first catalyst and comprising 0.1-3 weight percent platinum, 0.1-3 weight percent rhenium, and 1.25-2.0 weight percent chloride on an alumina carrier at dehydrogenation conditions including a temperature at least 25° F above said isomerization hydrogen temperature and in the range from about 775° F to 950° F and a pressure not higher than said isomerization hydrogen pressure; and c. recovering said first isomer from said final product mixture.
Claim 3
Dependent Claim 13 words
A process according to claim 1 wherein said selected xylene isomer is paraxylene.
Claim 4
Dependent Claim 28 words
A process according to claim 1 wherein the weight ratio of C 8 naphthenes to C 8 alkylaromatics in said intermediate reaction mixture is between 1:33 and 1:20.

References Cited (Backward Citations)

USRE25753E Cited
US3078318A Cited
US3642925A Cited
US3766287A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1980-12-12 1981-06-13 1981-12-13 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1984-12-12 1985-06-13 1985-12-13 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1988-12-12 1989-06-13 1989-12-13 $7700.00 Window Closed / Lapsed

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