SU1082309A3 - Способ получени палладиевого катализатора - Google Patents
Способ получени палладиевого катализатора Download PDFInfo
- Publication number
- SU1082309A3 SU1082309A3 SU762325903A SU2325903A SU1082309A3 SU 1082309 A3 SU1082309 A3 SU 1082309A3 SU 762325903 A SU762325903 A SU 762325903A SU 2325903 A SU2325903 A SU 2325903A SU 1082309 A3 SU1082309 A3 SU 1082309A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- catalyst
- palladium
- acetate
- nitrogen
- carrier
- Prior art date
Links
- 239000003054 catalyst Substances 0.000 title claims abstract description 81
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 title claims abstract description 48
- 229910052763 palladium Inorganic materials 0.000 title claims abstract description 26
- 238000000034 method Methods 0.000 title description 7
- 239000000203 mixture Substances 0.000 claims abstract description 20
- 239000003638 chemical reducing agent Substances 0.000 claims abstract description 12
- 239000011261 inert gas Substances 0.000 claims abstract description 12
- 238000001035 drying Methods 0.000 claims abstract description 11
- 239000007789 gas Substances 0.000 claims abstract description 8
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 27
- 239000001257 hydrogen Substances 0.000 claims description 10
- 229910052739 hydrogen Inorganic materials 0.000 claims description 10
- 150000001336 alkenes Chemical class 0.000 claims description 8
- -1 PALLADIUM CARBOXYLATE Chemical class 0.000 claims description 7
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 6
- 239000012190 activator Substances 0.000 claims description 3
- 230000000694 effects Effects 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 150000001735 carboxylic acids Chemical class 0.000 claims 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract description 67
- 229910052700 potassium Inorganic materials 0.000 abstract description 11
- 229910052748 manganese Inorganic materials 0.000 abstract description 8
- 229910052793 cadmium Inorganic materials 0.000 abstract description 7
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 abstract description 7
- 235000012239 silicon dioxide Nutrition 0.000 abstract description 7
- 229910052797 bismuth Inorganic materials 0.000 abstract description 4
- 239000013557 residual solvent Substances 0.000 abstract description 3
- 229910052720 vanadium Inorganic materials 0.000 abstract description 3
- 150000002941 palladium compounds Chemical class 0.000 abstract description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 abstract 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 125000001931 aliphatic group Chemical group 0.000 abstract 1
- 239000003610 charcoal Substances 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 235000019253 formic acid Nutrition 0.000 abstract 1
- 239000007792 gaseous phase Substances 0.000 abstract 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 48
- 229910052757 nitrogen Inorganic materials 0.000 description 23
- SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 description 20
- YJVFFLUZDVXJQI-UHFFFAOYSA-L palladium(ii) acetate Chemical compound [Pd+2].CC([O-])=O.CC([O-])=O YJVFFLUZDVXJQI-UHFFFAOYSA-L 0.000 description 13
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 12
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 10
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 10
- 239000011591 potassium Substances 0.000 description 10
- 235000011056 potassium acetate Nutrition 0.000 description 10
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 8
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 8
- 239000005977 Ethylene Substances 0.000 description 8
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 8
- 239000001301 oxygen Substances 0.000 description 8
- 229910052760 oxygen Inorganic materials 0.000 description 8
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 7
- 229910052788 barium Inorganic materials 0.000 description 7
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 7
- LHQLJMJLROMYRN-UHFFFAOYSA-L cadmium acetate Chemical compound [Cd+2].CC([O-])=O.CC([O-])=O LHQLJMJLROMYRN-UHFFFAOYSA-L 0.000 description 7
- 239000011572 manganese Substances 0.000 description 7
- 229940071125 manganese acetate Drugs 0.000 description 7
- UOGMEBQRZBEZQT-UHFFFAOYSA-L manganese(2+);diacetate Chemical compound [Mn+2].CC([O-])=O.CC([O-])=O UOGMEBQRZBEZQT-UHFFFAOYSA-L 0.000 description 7
- 239000011148 porous material Substances 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 6
- 241000269808 Sparus Species 0.000 description 6
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 5
- 229910002092 carbon dioxide Inorganic materials 0.000 description 5
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 4
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 4
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 4
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 239000001569 carbon dioxide Substances 0.000 description 4
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 4
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 3
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 3
- 229910052737 gold Inorganic materials 0.000 description 3
- 239000010931 gold Substances 0.000 description 3
- 150000002431 hydrogen Chemical class 0.000 description 3
- 229910052756 noble gas Inorganic materials 0.000 description 3
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 3
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- QYIGOGBGVKONDY-UHFFFAOYSA-N 1-(2-bromo-5-chlorophenyl)-3-methylpyrazole Chemical compound N1=C(C)C=CN1C1=CC(Cl)=CC=C1Br QYIGOGBGVKONDY-UHFFFAOYSA-N 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- FERIUCNNQQJTOY-UHFFFAOYSA-M Butyrate Chemical compound CCCC([O-])=O FERIUCNNQQJTOY-UHFFFAOYSA-M 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 239000001273 butane Substances 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 238000006555 catalytic reaction Methods 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003245 coal Substances 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- 239000012299 nitrogen atmosphere Substances 0.000 description 2
- JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Inorganic materials O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 description 2
- 150000002940 palladium Chemical class 0.000 description 2
- ZVSLRJWQDNRUDU-UHFFFAOYSA-L palladium(2+);propanoate Chemical compound [Pd+2].CCC([O-])=O.CCC([O-])=O ZVSLRJWQDNRUDU-UHFFFAOYSA-L 0.000 description 2
- JKDRQYIYVJVOPF-FDGPNNRMSA-L palladium(ii) acetylacetonate Chemical compound [Pd+2].C\C([O-])=C\C(C)=O.C\C([O-])=C\C(C)=O JKDRQYIYVJVOPF-FDGPNNRMSA-L 0.000 description 2
- PMJHHCWVYXUKFD-UHFFFAOYSA-N piperylene Natural products CC=CC=C PMJHHCWVYXUKFD-UHFFFAOYSA-N 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000001294 propane Substances 0.000 description 2
- 235000019260 propionic acid Nutrition 0.000 description 2
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000000741 silica gel Substances 0.000 description 2
- 229910002027 silica gel Inorganic materials 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 description 2
- PMJHHCWVYXUKFD-SNAWJCMRSA-N (E)-1,3-pentadiene Chemical group C\C=C\C=C PMJHHCWVYXUKFD-SNAWJCMRSA-N 0.000 description 1
- POILWHVDKZOXJZ-ARJAWSKDSA-M (z)-4-oxopent-2-en-2-olate Chemical compound C\C([O-])=C\C(C)=O POILWHVDKZOXJZ-ARJAWSKDSA-M 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- AUIZLSZEDUYGDE-UHFFFAOYSA-L cadmium(2+);diacetate;dihydrate Chemical compound O.O.[Cd+2].CC([O-])=O.CC([O-])=O AUIZLSZEDUYGDE-UHFFFAOYSA-L 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 239000001282 iso-butane Substances 0.000 description 1
- JMMWKPVZQRWMSS-UHFFFAOYSA-N isopropyl acetate Chemical compound CC(C)OC(C)=O JMMWKPVZQRWMSS-UHFFFAOYSA-N 0.000 description 1
- 229940046892 lead acetate Drugs 0.000 description 1
- 229940082328 manganese acetate tetrahydrate Drugs 0.000 description 1
- CESXSDZNZGSWSP-UHFFFAOYSA-L manganese(2+);diacetate;tetrahydrate Chemical compound O.O.O.O.[Mn+2].CC([O-])=O.CC([O-])=O CESXSDZNZGSWSP-UHFFFAOYSA-L 0.000 description 1
- 150000002835 noble gases Chemical class 0.000 description 1
- HVAMZGADVCBITI-UHFFFAOYSA-M pent-4-enoate Chemical compound [O-]C(=O)CCC=C HVAMZGADVCBITI-UHFFFAOYSA-M 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 150000004672 propanoic acids Chemical class 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000005406 washing Methods 0.000 description 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
- B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
- B01J37/02—Impregnation, coating or precipitation
- B01J37/0201—Impregnation
- B01J37/0203—Impregnation the impregnation liquid containing organic compounds
-
- 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
- B01J23/44—Palladium
-
- 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
- B01J23/54—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
- B01J23/56—Platinum group metals
- B01J23/58—Platinum group metals with alkali- or alkaline earth metals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/04—Preparation of carboxylic acid esters by reacting carboxylic acids or symmetrical anhydrides onto unsaturated carbon-to-carbon bonds
- C07C67/05—Preparation of carboxylic acid esters by reacting carboxylic acids or symmetrical anhydrides onto unsaturated carbon-to-carbon bonds with oxidation
- C07C67/055—Preparation of carboxylic acid esters by reacting carboxylic acids or symmetrical anhydrides onto unsaturated carbon-to-carbon bonds with oxidation in the presence of platinum group metals or their compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2509251A DE2509251C3 (de) | 1975-03-04 | 1975-03-04 | Verfahren zur Herstellung eines Palladiumkatalysators |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU1082309A3 true SU1082309A3 (ru) | 1984-03-23 |
Family
ID=5940367
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU762325903A SU1082309A3 (ru) | 1975-03-04 | 1976-02-23 | Способ получени палладиевого катализатора |
Country Status (27)
| Country | Link |
|---|---|
| US (1) | US4093559A (enExample) |
| JP (1) | JPS5911342B2 (enExample) |
| AR (1) | AR209347A1 (enExample) |
| AU (1) | AU502067B2 (enExample) |
| BE (1) | BE839191A (enExample) |
| BG (1) | BG25200A3 (enExample) |
| BR (1) | BR7601290A (enExample) |
| CA (1) | CA1070659A (enExample) |
| CS (1) | CS195723B2 (enExample) |
| DD (1) | DD123573A5 (enExample) |
| DE (1) | DE2509251C3 (enExample) |
| DK (1) | DK153370C (enExample) |
| ES (1) | ES445603A1 (enExample) |
| FR (1) | FR2302781A1 (enExample) |
| GB (1) | GB1535584A (enExample) |
| HU (1) | HU179197B (enExample) |
| IE (1) | IE42499B1 (enExample) |
| IT (1) | IT1056816B (enExample) |
| LU (1) | LU74458A1 (enExample) |
| NL (1) | NL7602049A (enExample) |
| NO (1) | NO146845C (enExample) |
| PL (1) | PL99997B1 (enExample) |
| RO (1) | RO70540A (enExample) |
| SE (1) | SE415450B (enExample) |
| SU (1) | SU1082309A3 (enExample) |
| YU (1) | YU39203B (enExample) |
| ZA (1) | ZA761267B (enExample) |
Families Citing this family (44)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5379785A (en) * | 1976-12-24 | 1978-07-14 | Kurashiki Boseki Kk | Catalyst carrying method |
| FR2442658A1 (fr) * | 1978-11-30 | 1980-06-27 | Chinoin Gyogyszer Es Vegyeszet | Procede pour la preparation de catalyseurs au palladium non-pyrophores |
| US4379778A (en) * | 1980-10-10 | 1983-04-12 | Air Products And Chemicals, Inc. | Hydrogen peroxide synthesis |
| FR2505205B1 (fr) * | 1981-05-05 | 1986-05-23 | Inst Francais Du Petrole | Nouveaux catalyseurs de metaux nobles du groupe viii supportes a haute dispersion et grande activite leur fabrication et leur utilisation notamment dans les reactions d'hydrogenation |
| US4476242A (en) * | 1981-10-29 | 1984-10-09 | Standard Oil Company (Indiana) | Process for preparing palladium on carbon catalysts for purification of crude terephthalic acid |
| US4415479A (en) * | 1981-10-29 | 1983-11-15 | Standard Oil Company (Indiana) | Palladium on carbon catalyst for purification of crude terephthalic acid |
| US4656153A (en) * | 1983-02-28 | 1987-04-07 | Standard Oil Company (Indiana) | Active carbon containing a dispersion of a metal component and method for making same |
| CA1234797A (en) * | 1983-12-07 | 1988-04-05 | Sun Refining And Marketing Company | CATALYTIC OXIDATION OF OLEFINS TO .alpha.,.beta.-UNSATURATED CARBOXYLIC ACIDS |
| CA1237146A (en) * | 1983-12-07 | 1988-05-24 | James E. Lyons | Catalytic oxidation of propylene to allyl acetate |
| CA1238052A (en) * | 1983-12-07 | 1988-06-14 | Sun Refining And Marketing Company | INCREASED SELECTIVITIES IN THE OXIDATION OF OLEFINS TO .alpha.,.beta.-UNSATURATED CARBOXYLIC ACIDS |
| US4732883A (en) * | 1983-12-07 | 1988-03-22 | Sun Refining And Marketing Company | Catalytic oxidation of propylene to allyl acetate |
| CA1236849A (en) * | 1983-12-07 | 1988-05-17 | James E. Lyons | Process for the oxidation of butenes to linear acetates |
| CA1238053A (en) * | 1983-12-07 | 1988-06-14 | Sun Refining And Marketing Company | INCREASED SELECTIVITIES IN THE OXIDATION OF OLEFINS TO .alpha.,.beta.-UNSATURATED CARBOXYLIC ACIDS |
| US4713363A (en) * | 1984-12-27 | 1987-12-15 | The Dow Chemical Company | High surface area supported noble metal catalysts and process for their preparation |
| US4714695A (en) * | 1985-04-18 | 1987-12-22 | The Standard Oil Company | Method for the preparation of high activity palladium based catalysts |
| US4623635A (en) | 1985-04-18 | 1986-11-18 | The Standard Oil Company | Method for the preparation of high activity palladium based catalysts |
| JPS6434443A (en) * | 1987-07-14 | 1989-02-03 | Lonza Ag | Catalyst for oxidizing carbon compound |
| US4916108A (en) * | 1988-08-25 | 1990-04-10 | Westinghouse Electric Corp. | Catalyst preparation using supercritical solvent |
| US5225388A (en) * | 1989-12-05 | 1993-07-06 | Hoechst Aktiengesellschaft | Method for making a catalyst |
| US5149854A (en) * | 1990-12-10 | 1992-09-22 | Mooney Chemicals, Inc. | Preparation of platinum group metal and rhenium carboxylates |
| US5194417A (en) * | 1991-12-05 | 1993-03-16 | Quantum Chemical Corporation | Pretreatment of palladium-gold catalysts useful in vinyl acetate synthesis |
| US5600692A (en) * | 1993-10-29 | 1997-02-04 | General Electric Company | Method for improving tenacity and loading of palladium on palladium-doped metal surfaces |
| US5600691A (en) * | 1993-10-29 | 1997-02-04 | General Electric Company | Noble metal doping or coating of crack interior for stress corrosion cracking protection of metals |
| US5773096A (en) * | 1993-10-29 | 1998-06-30 | General Electric Company | Method of catalyst preparation by high-temperature hydrothermal incorporation of noble metals onto surfaces and matrices |
| US5818893A (en) * | 1993-10-29 | 1998-10-06 | General Electric Company | In-situ palladium doping or coating of stainless steel surfaces |
| US5448605A (en) * | 1993-10-29 | 1995-09-05 | General Electric Company | Palladium acetylacetonate solution and related method of manufacture |
| US5608766A (en) * | 1993-10-29 | 1997-03-04 | General Electric Company | Co-deposition of palladium during oxide film growth in high-temperature water to mitigate stress corrosion cracking |
| US5602888A (en) * | 1993-10-29 | 1997-02-11 | General Electric Company | Radiation-induced palladium doping of metals to protect against stress corrosion cracking |
| CA2135021A1 (en) * | 1993-11-19 | 1995-05-20 | David J. Gulliver | Process for the preparation of catalysts for use in the production of vinyl acetate |
| US5643849A (en) * | 1994-07-25 | 1997-07-01 | Lever Brothers Company, Division Of Conopco, Inc. | Catalysts and improved process for preparing salts of aldonic acid |
| US5688993A (en) * | 1995-12-22 | 1997-11-18 | E. I. Du Pont De Nemours And Company | Method for modifying catalyst performance during the gas phase synthesis of vinyl acetate |
| ITMI971161A1 (it) * | 1997-05-19 | 1998-11-19 | Montecatini Tecnologie Srl | Catalizzatori di idrogenazione |
| EP1015109A1 (de) * | 1997-09-12 | 2000-07-05 | Institut für Umwelttechnologie und Umweltanalytik e.V. (IUTA) | Verfahren und vorrichtung zur katalytischen abgasreinigung |
| US5948724A (en) * | 1997-10-28 | 1999-09-07 | Celanese International Corporation | Vinyl acetate catalyst comprising metallic palladium and gold and cupric acetate |
| US6072078A (en) * | 1997-12-12 | 2000-06-06 | Celanese International Corporation | Vinyl acetate production using a catalyst comprising palladium, gold, copper and any of certain fourth metals |
| GB9810928D0 (en) * | 1998-05-22 | 1998-07-22 | Bp Chem Int Ltd | Catalyst and process |
| ID26891A (id) * | 1998-06-02 | 2001-02-15 | Celanese Internasional Corp | Katalis vinil asetat yang terdiri dari palladium logam dan emas yang dibuat dengan potasium aurat |
| US6017847A (en) * | 1998-06-02 | 2000-01-25 | Celanese International Corporation | Vinyl acetate catalyst prepared with potassium aurate and comprising metallic palladium and gold on a carrier precoated with copper |
| TW471982B (en) | 1998-06-02 | 2002-01-11 | Dairen Chemical Corp | Catalyst manufacture method and its use for preparing vinyl acetate |
| DE19920390C2 (de) * | 1999-05-04 | 2002-08-01 | Celanese Chem Europe Gmbh | Katalysator und Verfahren zur Herstellung von Vinylacetat |
| US7605106B2 (en) * | 2005-11-15 | 2009-10-20 | Nova Chemicals (International) S.A. | Telomerization of dienes |
| DE102006058800A1 (de) * | 2006-12-13 | 2008-06-19 | Wacker Chemie Ag | Verfahren zur Herstellung von Katalysatoren und deren Verwendung für die Gasphasenoxidation von Olefinen |
| DE102014223759A1 (de) | 2014-11-20 | 2016-05-25 | Wacker Chemie Ag | Entfernung von Sauerstoff aus Kohlenwasserstoff-haltigen Gasgemischen |
| US10358398B2 (en) * | 2016-05-17 | 2019-07-23 | Iowa State University Research Foundation, Inc. | Dehydrogenation of propane using a metal-containing catalyst on a support |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1618589A1 (de) * | 1967-04-01 | 1971-02-25 | Knapsack Ag | Verfahren zur Herstellung von Carbonsaeuren |
| DE1667053C3 (de) * | 1967-12-02 | 1975-10-09 | Hoechst Ag, 6000 Frankfurt | Verfahren zur Herstellung eines Palladiumkatalysators |
| GB1236989A (en) * | 1967-12-02 | 1971-06-23 | Hoechst Ag | Improvements in and relating to catalysts |
| DE1901289C3 (de) * | 1969-01-11 | 1981-05-27 | Bayer Ag, 5090 Leverkusen | Verfahren zur Herstellung vo Allylacetat |
| DE1911178A1 (de) * | 1969-03-05 | 1970-09-24 | Bayer Ag | Verfahren zur Herstellung von Allylacetat |
| GB1333449A (en) * | 1970-11-20 | 1973-10-10 | Hoechst Ag | Process for the oxacylation of olefins in the gaseous phase |
| DE2107913C3 (de) * | 1971-02-19 | 1979-10-04 | Bayer Ag, 5090 Leverkusen | Verfahren zur Herstellung von Benzylacetat |
| DE2238837A1 (de) * | 1972-08-07 | 1974-02-14 | Roehm Gmbh | Verfahren zur herstellung alpha,betaungesaettigter carbonsaeuren |
| US3862252A (en) * | 1972-12-28 | 1975-01-21 | Kanegafuchi Chemical Ind | Method of selective hydrogenation of cyclopentadiene |
| US3849343A (en) * | 1973-02-05 | 1974-11-19 | Universal Oil Prod Co | Method of catalyst manufacture |
| US3931054A (en) * | 1974-04-19 | 1976-01-06 | Universal Oil Products Company | Method of catalyst manufacture |
| US3998759A (en) * | 1975-01-29 | 1976-12-21 | Universal Oil Products Company | Method of catalyst manufacture |
-
1975
- 1975-03-04 DE DE2509251A patent/DE2509251C3/de not_active Expired
-
1976
- 1976-02-14 RO RO7684817A patent/RO70540A/ro unknown
- 1976-02-23 SU SU762325903A patent/SU1082309A3/ru active
- 1976-02-25 SE SE7602343A patent/SE415450B/xx not_active IP Right Cessation
- 1976-02-27 DD DD191622A patent/DD123573A5/xx unknown
- 1976-02-27 BR BR7601290A patent/BR7601290A/pt unknown
- 1976-02-27 BG BG032477A patent/BG25200A3/xx unknown
- 1976-02-27 ES ES445603A patent/ES445603A1/es not_active Expired
- 1976-02-27 NL NL7602049A patent/NL7602049A/xx not_active Application Discontinuation
- 1976-03-02 CA CA246,930A patent/CA1070659A/en not_active Expired
- 1976-03-02 IT IT20778/76A patent/IT1056816B/it active
- 1976-03-02 US US05/663,117 patent/US4093559A/en not_active Expired - Lifetime
- 1976-03-02 LU LU74458A patent/LU74458A1/xx unknown
- 1976-03-03 AU AU11620/76A patent/AU502067B2/en not_active Expired
- 1976-03-03 JP JP51022297A patent/JPS5911342B2/ja not_active Expired
- 1976-03-03 PL PL1976187679A patent/PL99997B1/pl unknown
- 1976-03-03 NO NO760718A patent/NO146845C/no unknown
- 1976-03-03 AR AR262428A patent/AR209347A1/es active
- 1976-03-03 HU HU76HO1885A patent/HU179197B/hu not_active IP Right Cessation
- 1976-03-03 IE IE428/76A patent/IE42499B1/en unknown
- 1976-03-03 ZA ZA761267A patent/ZA761267B/xx unknown
- 1976-03-03 CS CS761394A patent/CS195723B2/cs unknown
- 1976-03-03 DK DK090876A patent/DK153370C/da not_active IP Right Cessation
- 1976-03-04 FR FR7606097A patent/FR2302781A1/fr active Granted
- 1976-03-04 BE BE164858A patent/BE839191A/xx not_active IP Right Cessation
- 1976-03-04 GB GB8687/76A patent/GB1535584A/en not_active Expired
- 1976-03-04 YU YU546/76A patent/YU39203B/xx unknown
Non-Patent Citations (1)
| Title |
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| 1. Патент СССР № 291407, кл. В О J 37/02, опублик. 1971. 2. Патент DE № 1668088, кл. 120, 19/03, -опублик. 1974 (прототип) . * |
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