US4038208A
Expired / Lapsed
US
⏱️ 0.0 years remaining
Processes for regenerating dispersions of ligand-stabilized, palladium(ii) halide complexes used in carbonylation catalysts
Assignee: Texaco Inc
•
Filing: 1975-11-28
•
Granted: 1977-07-26
•
Expires: 1995-11-28
Abstract
Abstract This invention concerns processes for regeneration of carbonylation catalysts consisting of dispersions of ligand-stabilized palladium(II) halide complexes in quaternary ammonium, phosphonium and arsonium salts of trihalostannate(II) and trihalogermanate(II) using hydrogen peroxide as the regenerating agent.
Inventors
- 👤 John F. Knifton
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-11-03 23:10
CPC Classifications
B; B01; B01J; B01J31/00; B01J31/16; B01J31/24; B01J31/2404; B01J31/02; B01J31/0234; B01J31/0235; B01J31/0239; B01J31/0255; B01J31/0267; B01J31/0268; B01J31/18; B01J31/1895; B01J31/26; B01J31/40; B01J31/4015; B01J31/4023; B01J31/4038; B01J31/4053; B01J2231/00; B01J2231/30; B01J2231/32; B01J2231/321; B01J2531/00; B01J2531/80; B01J2531/82; B01J2531/824; B01J27/00; B01J27/06; B01J27/08; B01J27/10
Claims Analysis
Total Claims: 4
Claim 1
Independent Claim
288 words
A process for regenerating spent palladium carbonylation catalysts consisting of dispersions of ligand-stabilized palladium(II) halide catalyst complexes in quaternary ammonium, phosphonium, and arsonium salts of trihalostannate(II) and trihalogermanate(II), the spent catalyst being obtained from the carbonylation of olefins, said ligand-stabilixed catalysts being selected from the group consisting of: [(C 2 H 5 ) 4 N][SnCl 3 ]-PdCl 2 [P(C 6 H 5 ) 3 ] 2 [(c 2 h 5 ) 4 n][snCl 3 ]-PdCl 2 [P(p-CH 3 .C 6 H 4 ) 3 ] 2 [clCH 2 ( 6 H 5 ) 3 P][SnCl 3 ]-PdCl 2 [P(C 6 H 5 ) 3 ] 2 [(n-C 4 H 9 ) 4 N][SnCl 3 ]-PdCl 2 [P(C 6 H 5 ) 3 ] 2 (c 6 h 5 ) 4 as][SnCl 3 ]-PdCl 2 [P(C 6 H 5 ) 3 ] 2 [(c 2 h 5 ) 4 n][geCl 3 ]-PdCl 2 [P(C 6 H 5 ) 3 ] 2 [(c 2 h 5 ) 4 n][snCl 3 ]-PdCl 2 [P(p-CH 3 O.C 6 H 4 ) 3 ] 2 , and [(C 7 H 15 ) 4 N][GeCl 3 ]-PdCl 2 [As(C 6 H 5 ) 3 ] 2 , by the steps of: (a) Contacting said spent catalyst with an aqueous solution of hydrogen peroxide at 20° to 150° C in the mole ratio of 1-10 4 mole of peroxide per gram atom of palladium present in said catalyst. (b) Adding additional stabilizing ligand to the solid catalyst in the mole ratio of 1-10 mole of ligand per gram atom of palladium present, said stabilizing ligand being selected from the group consisting of triphenylphosphine, triphenylarsine, tri-p-tolylphosphine and tri-p-methoxyphenylphosphine, until the spent palladium carbonylation catalyst is regenerated.
Claim 2
Dependent Claim
288 words
A process for regenerating spent palladium carbonylation catalysts consisting of dispersions of ligand-stabilized palladium(II) halide catalyst complexes in quaternary ammonium, phosphonium, and arsonium salts of trihalostannate(II) and trihalogermanate(II), the spent catalyst being obtained from the carbonylation of olefins, said ligand-stabilixed catalysts being selected from the group consisting of: [(C 2 H 5 ) 4 N][SnCl 3 ]-PdCl 2 [P(C 6 H 5 ) 3 ] 2 [(c 2 h 5 ) 4 n][snCl 3 ]-PdCl 2 [P(p-CH 3 .C 6 H 4 ) 3 ] 2 [clCH 2 ( 6 H 5 ) 3 P][SnCl 3 ]-PdCl 2 [P(C 6 H 5 ) 3 ] 2 [(n-C 4 H 9 ) 4 N][SnCl 3 ]-PdCl 2 [P(C 6 H 5 ) 3 ] 2 (c 6 h 5 ) 4 as][SnCl 3 ]-PdCl 2 [P(C 6 H 5 ) 3 ] 2 [(c 2 h 5 ) 4 n][geCl 3 ]-PdCl 2 [P(C 6 H 5 ) 3 ] 2 [(c 2 h 5 ) 4 n][snCl 3 ]-PdCl 2 [P(p-CH 3 O.C 6 H 4 ) 3 ] 2 , and [(C 7 H 15 ) 4 N][GeCl 3 ]-PdCl 2 [As(C 6 H 5 ) 3 ] 2 , by the steps of: (a) Contacting said spent catalyst with an aqueous solution of hydrogen peroxide at 20° to 150° C in the mole ratio of 1-10 4 mole of peroxide per gram atom of palladium present in said catalyst. (b) Adding additional stabilizing ligand to the solid catalyst in the mole ratio of 1-10 mole of ligand per gram atom of palladium present, said stabilizing ligand being selected from the group consisting of triphenylphosphine, triphenylarsine, tri-p-tolylphosphine and tri-p-methoxyphenylphosphine, until the spent palladium carbonylation catalyst is regenerated.
Claim 3
Dependent Claim
24 words
The process of claim 1 wherein the added hydrogen peroxide reagent is dissolved in an aqueous media in 1 to 90% concentration by volume.
Claim 4
Dependent Claim
25 words
The process of claim 1 wherein the amount of aqueous solution of hydrogen peroxide is reduced by distillation prior to the addition of stabilizing ligand.
References Cited (Backward Citations)
US3455989A
Cited
US3420873A
Cited
US3832391A
Cited
US3700706A
Cited
US3641076A
Cited
US3968133A
Cited
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1980-07-25 | 1981-01-24 | 1981-07-26 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1984-07-25 | 1985-01-24 | 1985-07-26 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1988-07-25 | 1989-01-24 | 1989-07-26 | $7700.00 | Window Closed / Lapsed |