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US4497969A Expired / Lapsed US ⏱️ 0.0 years remaining

Process for the production of catalysts based on crystalline aluminosilicates and the use of catalyst so produced

Assignee: BP PLC
•
Filing: 1984-03-27
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Granted: 1985-02-05
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Expires: 2004-03-27
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Abstract

Abstract A process for the production of a catalyst based on a crystalline aluminosilicate having a silica to alumina molar ratio greater than 12:1 which is obtained by mixing a source of silica, a source of alumina, a source of alkali metal, water and a source of ammonium ions in defined proportions, crystallizing the mixture, recovering the crystalline aluminosilicate so-formed, cation-exchanging and/or impregnating the recovered crystalline aluminosilicate and finally calcining, wherein either the recovered crystalline aluminosilicate or the cation-exchanged aluminosilicate or the impregnated aluminosilicate is washed with a solution containing either an organic base, a carboxylic acid, an alcohol, a glycol, a phenol or an ester. The washing treatment results in a reduction in the rate of decline in catalytic activity in reactions such as the conversion of aliphatic to aromatic hydrocarbons.

Inventors

  • 👤 William J. Ball
  • 👤 David G. Stewart

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-02 23:25
CPC Classifications
B; B01; B01J; B01J29/00; B01J29/87; B01J29/04; B01J29/06; B01J29/40; C; C07; C07C; C07C2/00; C07C2529/00; C07C2529/04; C07C2529/06

Claims Analysis

Total Claims: 2
Claim 1
Independent Claim 281 words
In a process for the production of aromatic hydrocarbons at elevated temperature and in the vapor phase by contacting a C 2 to C 12 aliphatic hydrocarbon feedstock with a catalyst, the improvement which comprises employing as the catalyst a crystalline aluminosilicate having a silica to alumina molar ratio greater than 12:1 which crystalline aluminosilicate is obtained by mixing a source of silica, a source of alumina, a source of alkali metal, water and a source of ammonium ions in the absence of an alcohol or an alkylene oxide in the molar proportions expressed in the case of the silica and alumina sources in terms of the equivalent moles of the oxide, in the case of the alkali metal source in terms of the equivalent moles of the hydroxide, MOH, and in the case of the source of ammonium ions in terms of free ammonia: SiO 2 :Al 2 O 3 greater than 12:1 MOH:Al 2 O 3 in the range from 1:1 to 20:1 SiO 2 :NH 3 in the range from 1:1 to 200:1, and H 2 O:MOH in the range from 30:1 to 300:1, maintaining the mixture at elevated temperature for a period such that crystallisation occurs, recovering the crystalline aluminosilicate so-formed, cation-exchanging the recovered crystalline aluminosilicate with either gallium or aluminum cations and/or impregnating the recovered crystalline aluminosilicate with a solution of a gallium or aluminum compound and finally calcining the exchanged and/or impregnated crystalline aluminosilicate characterised in that either the recovered crystalline aluminosilicate or the cation-exchanged crystalline aluminosilicate or the metal impregnated crystalline aluminosilicate is washed with a solution containing either an organic base, a carboxylic acid, an alcohol, a glycol, a phenol or an ester.
Claim 2
Dependent Claim 281 words
In a process for the production of aromatic hydrocarbons at elevated temperature and in the vapor phase by contacting a C 2 to C 12 aliphatic hydrocarbon feedstock with a catalyst, the improvement which comprises employing as the catalyst a crystalline aluminosilicate having a silica to alumina molar ratio greater than 12:1 which crystalline aluminosilicate is obtained by mixing a source of silica, a source of alumina, a source of alkali metal, water and a source of ammonium ions in the absence of an alcohol or an alkylene oxide in the molar proportions expressed in the case of the silica and alumina sources in terms of the equivalent moles of the oxide, in the case of the alkali metal source in terms of the equivalent moles of the hydroxide, MOH, and in the case of the source of ammonium ions in terms of free ammonia: SiO 2 :Al 2 O 3 greater than 12:1 MOH:Al 2 O 3 in the range from 1:1 to 20:1 SiO 2 :NH 3 in the range from 1:1 to 200:1, and H 2 O:MOH in the range from 30:1 to 300:1, maintaining the mixture at elevated temperature for a period such that crystallisation occurs, recovering the crystalline aluminosilicate so-formed, cation-exchanging the recovered crystalline aluminosilicate with either gallium or aluminum cations and/or impregnating the recovered crystalline aluminosilicate with a solution of a gallium or aluminum compound and finally calcining the exchanged and/or impregnated crystalline aluminosilicate characterised in that either the recovered crystalline aluminosilicate or the cation-exchanged crystalline aluminosilicate or the metal impregnated crystalline aluminosilicate is washed with a solution containing either an organic base, a carboxylic acid, an alcohol, a glycol, a phenol or an ester.

References Cited (Backward Citations)

US3509042A Cited
US3213013A Cited
US3264208A Cited
US3360484A Cited
US4341748A Cited
US4452907A Cited
US4452908A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1988-02-05 1988-08-06 1989-02-05 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1992-02-05 1992-08-06 1993-02-05 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1996-02-05 1996-08-06 1997-02-05 $7700.00 Window Closed / Lapsed

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