GB1066579A - Catalyst - Google Patents
CatalystInfo
- Publication number
- GB1066579A GB1066579A GB4585064A GB4585064A GB1066579A GB 1066579 A GB1066579 A GB 1066579A GB 4585064 A GB4585064 A GB 4585064A GB 4585064 A GB4585064 A GB 4585064A GB 1066579 A GB1066579 A GB 1066579A
- Authority
- GB
- United Kingdom
- Prior art keywords
- carbon
- alkylation
- rh2s3
- catalyst
- hydrogen
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 239000003054 catalyst Substances 0.000 title abstract 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 3
- 229910052799 carbon Inorganic materials 0.000 abstract 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- 230000029936 alkylation Effects 0.000 abstract 2
- 238000005804 alkylation reaction Methods 0.000 abstract 2
- 238000006243 chemical reaction Methods 0.000 abstract 2
- 230000000694 effects Effects 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 abstract 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 abstract 1
- 229910021604 Rhodium(III) chloride Inorganic materials 0.000 abstract 1
- 239000007864 aqueous solution Substances 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 239000012452 mother liquor Substances 0.000 abstract 1
- ATGUVEKSASEFFO-UHFFFAOYSA-N p-aminodiphenylamine Chemical compound C1=CC(N)=CC=C1NC1=CC=CC=C1 ATGUVEKSASEFFO-UHFFFAOYSA-N 0.000 abstract 1
- 239000002245 particle Substances 0.000 abstract 1
- 238000005932 reductive alkylation reaction Methods 0.000 abstract 1
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 abstract 1
- 150000003284 rhodium compounds Chemical class 0.000 abstract 1
- SONJTKJMTWTJCT-UHFFFAOYSA-K rhodium(iii) chloride Chemical compound [Cl-].[Cl-].[Cl-].[Rh+3] SONJTKJMTWTJCT-UHFFFAOYSA-K 0.000 abstract 1
- 229910052979 sodium sulfide Inorganic materials 0.000 abstract 1
- GRVFOGOEDUUMBP-UHFFFAOYSA-N sodium sulfide (anhydrous) Chemical compound [Na+].[Na+].[S-2] GRVFOGOEDUUMBP-UHFFFAOYSA-N 0.000 abstract 1
- 238000001179 sorption measurement Methods 0.000 abstract 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- B01J27/02—Sulfur, selenium or tellurium; Compounds thereof
- B01J27/04—Sulfides
- B01J27/043—Sulfides with iron group metals or platinum group metals
- B01J27/045—Platinum group metals
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
- B01J23/40—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals of the platinum group metals
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
- B01J23/40—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals of the platinum group metals
- B01J23/46—Ruthenium, rhodium, osmium or iridium
- B01J23/464—Rhodium
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J21/00—Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
- B01J21/18—Carbon
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/20—Sulfiding
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Specially prepared catalysts consisting of Rh2S3 on carbon are used to effect reductive alkylation of p-amino diphenylamine with methyl isobutyl ketone in the presence of hydrogen. Reaction temperature of 180-185 DEG C. and pressure of 400-600 p.s.i.g. was recorded in the autoclave used to effect alkylation. Adsorption of hydrogen stopped when desired reaction was completed and yields were theoretical.ALSO:An alkylation catalyst consists of Rh2S3 on carbon and is made by reacting an alkaline sulphiding agent (e.g. Na2S, K2S or (NH4)2S) with an aqueous solution of a trivalent rhodium compound (e.g. RhCl3) in the presence of a particulate carbon support, and thereafter separating the sulphided rhodium on carbon from mother liquor. Physical data e.g. particle size and surface area of the catalyst are disclosed.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US32305763A | 1963-11-12 | 1963-11-12 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1066579A true GB1066579A (en) | 1967-04-26 |
Family
ID=23257585
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB4585064A Expired GB1066579A (en) | 1963-11-12 | 1964-11-10 | Catalyst |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB1066579A (en) |
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0014998A1 (en) * | 1979-02-21 | 1980-09-03 | Uniroyal, Inc. | Preparation of tertiary aromatic amines by reductive alkylation of diaryl secondary amines with ketones |
| WO2000073538A1 (en) * | 1999-05-27 | 2000-12-07 | De Nora Elettrodi S.P.A. | Rhodium electrocatalyst and method of preparation |
| JP2004507621A (en) * | 2000-09-01 | 2004-03-11 | デ・ノラ・エレートローディ・ソチエタ・ペル・アツィオーニ | Method for electrolysis of industrial grade hydrochloric acid contaminated with organic substances using oxygen consuming cathode |
| WO2003040435A3 (en) * | 2001-11-07 | 2004-05-06 | De Nora Elettrodi Spa | Rhodium electrocatalyst and method of preparation |
| WO2005075071A1 (en) * | 2004-01-28 | 2005-08-18 | De Nora Elettrodi S.P.A. | Synthesis of noble metal sulphilde catalysts in a sulphide ion-free aqueous environment |
| CN100428988C (en) * | 2004-01-28 | 2008-10-29 | 德·诺拉电极股份公司 | Synthesis of noble metal sulfide catalysts in an aqueous environment free of divalent sulfide ions |
| CN104402068A (en) * | 2014-11-07 | 2015-03-11 | 中国海洋石油总公司 | Method for preparing high-purity rhodium trichloride from carbonyl-synthetic-reaction waste rhodium catalyst degradation solution |
| CN104478009A (en) * | 2014-11-07 | 2015-04-01 | 中国海洋石油总公司 | Method for recovering rhodium from rhodium-containing cationic resin exchange waste liquid |
| CN104478008A (en) * | 2014-11-07 | 2015-04-01 | 中国海洋石油总公司 | Method for preparing rhodium trichloride hydrate by using silica gel-polyamine resin |
| WO2025120164A1 (en) | 2023-12-08 | 2025-06-12 | Basf Se | Rhodium sulfides as hydroformylation catalysts |
-
1964
- 1964-11-10 GB GB4585064A patent/GB1066579A/en not_active Expired
Cited By (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0014998A1 (en) * | 1979-02-21 | 1980-09-03 | Uniroyal, Inc. | Preparation of tertiary aromatic amines by reductive alkylation of diaryl secondary amines with ketones |
| WO2000073538A1 (en) * | 1999-05-27 | 2000-12-07 | De Nora Elettrodi S.P.A. | Rhodium electrocatalyst and method of preparation |
| AU758776B2 (en) * | 1999-05-27 | 2003-03-27 | Industrie De Nora S.P.A. | Rhodium electrocatalyst and method of preparation |
| RU2230136C2 (en) * | 1999-05-27 | 2004-06-10 | Де Нора Элеттроди С.П.А. | Rhodium electrocatalitic agent and a method of its preparation |
| CN1303256C (en) * | 1999-05-27 | 2007-03-07 | 德·诺拉电极股份公司 | Rhodium electrocatalyst and method of preparation |
| JP2004507621A (en) * | 2000-09-01 | 2004-03-11 | デ・ノラ・エレートローディ・ソチエタ・ペル・アツィオーニ | Method for electrolysis of industrial grade hydrochloric acid contaminated with organic substances using oxygen consuming cathode |
| RU2311496C2 (en) * | 2001-11-07 | 2007-11-27 | Де Нора Элеттроди С.П.А. | Upgraded rhodium electrocatalyst and the method of its production |
| WO2003040435A3 (en) * | 2001-11-07 | 2004-05-06 | De Nora Elettrodi Spa | Rhodium electrocatalyst and method of preparation |
| CZ307526B6 (en) * | 2001-11-07 | 2018-11-14 | De Nora Elettrodi S.P.A. | An improved rhodium sulphide electrocatalyst and a process of its preparation |
| JP2007519514A (en) * | 2004-01-28 | 2007-07-19 | デ・ノラ・エレートローディ・ソチエタ・ペル・アツィオーニ | Synthesis of noble metal sulfide catalysts in aqueous environment free of sulfide ions |
| CN100428988C (en) * | 2004-01-28 | 2008-10-29 | 德·诺拉电极股份公司 | Synthesis of noble metal sulfide catalysts in an aqueous environment free of divalent sulfide ions |
| AU2005210090B2 (en) * | 2004-01-28 | 2009-06-11 | Industrie De Nora S.P.A. | Synthesis of noble metal sulphilde catalysts in a sulphide ion-free aqueous environment |
| RU2358802C2 (en) * | 2004-01-28 | 2009-06-20 | Де Нора Элеттроди С.П.А. | Catalyst synthesis on base of noble metals sulphides in sulphide ions-free water media |
| WO2005075071A1 (en) * | 2004-01-28 | 2005-08-18 | De Nora Elettrodi S.P.A. | Synthesis of noble metal sulphilde catalysts in a sulphide ion-free aqueous environment |
| CN104402068A (en) * | 2014-11-07 | 2015-03-11 | 中国海洋石油总公司 | Method for preparing high-purity rhodium trichloride from carbonyl-synthetic-reaction waste rhodium catalyst degradation solution |
| CN104478009A (en) * | 2014-11-07 | 2015-04-01 | 中国海洋石油总公司 | Method for recovering rhodium from rhodium-containing cationic resin exchange waste liquid |
| CN104478008A (en) * | 2014-11-07 | 2015-04-01 | 中国海洋石油总公司 | Method for preparing rhodium trichloride hydrate by using silica gel-polyamine resin |
| CN104402068B (en) * | 2014-11-07 | 2016-07-13 | 中国海洋石油总公司 | The method that carbongl group synthesis reaction spent rhodium catalyst digestion solution prepares high-purity rhodium chloride |
| WO2025120164A1 (en) | 2023-12-08 | 2025-06-12 | Basf Se | Rhodium sulfides as hydroformylation catalysts |
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