SU413656A3 - - Google Patents
Info
- Publication number
- SU413656A3 SU413656A3 SU1697505A SU1697505A SU413656A3 SU 413656 A3 SU413656 A3 SU 413656A3 SU 1697505 A SU1697505 A SU 1697505A SU 1697505 A SU1697505 A SU 1697505A SU 413656 A3 SU413656 A3 SU 413656A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- catalyst
- palladium
- carrier
- impregnated
- alumina
- Prior art date
Links
- 239000003054 catalyst Substances 0.000 description 24
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 18
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 10
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 10
- 229910052763 palladium Inorganic materials 0.000 description 9
- 239000000243 solution Substances 0.000 description 9
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 7
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 6
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- PIBWKRNGBLPSSY-UHFFFAOYSA-L palladium(II) chloride Chemical compound Cl[Pd]Cl PIBWKRNGBLPSSY-UHFFFAOYSA-L 0.000 description 4
- 229910052596 spinel Inorganic materials 0.000 description 4
- 239000011029 spinel Substances 0.000 description 4
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 3
- 238000002441 X-ray diffraction Methods 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000005984 hydrogenation reaction Methods 0.000 description 3
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
- 229910002651 NO3 Inorganic materials 0.000 description 2
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 239000010941 cobalt Substances 0.000 description 2
- 229910017052 cobalt Inorganic materials 0.000 description 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- DKAGJZJALZXOOV-UHFFFAOYSA-N hydrate;hydrochloride Chemical compound O.Cl DKAGJZJALZXOOV-UHFFFAOYSA-N 0.000 description 2
- 229910052744 lithium Inorganic materials 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- ONDPHDOFVYQSGI-UHFFFAOYSA-N zinc nitrate Chemical compound [Zn+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O ONDPHDOFVYQSGI-UHFFFAOYSA-N 0.000 description 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 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 241001137251 Corvidae Species 0.000 description 1
- 229910000611 Zinc aluminium Inorganic materials 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- HXFVOUUOTHJFPX-UHFFFAOYSA-N alumane;zinc Chemical compound [AlH3].[Zn] HXFVOUUOTHJFPX-UHFFFAOYSA-N 0.000 description 1
- HIGRAKVNKLCVCA-UHFFFAOYSA-N alumine Chemical compound C1=CC=[Al]C=C1 HIGRAKVNKLCVCA-UHFFFAOYSA-N 0.000 description 1
- 239000011260 aqueous acid Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- UFMZWBIQTDUYBN-UHFFFAOYSA-N cobalt dinitrate Chemical compound [Co+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O UFMZWBIQTDUYBN-UHFFFAOYSA-N 0.000 description 1
- 229910001981 cobalt nitrate Inorganic materials 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000012047 saturated solution Substances 0.000 description 1
- 238000002791 soaking 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
- 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
- B01J21/00—Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
- B01J21/005—Spinels
-
- 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
- B01J23/005—Spinels
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/006—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by hydrogenation of aromatic hydroxy 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 |
|---|---|---|---|
| DE19702045882 DE2045882C3 (de) | 1970-09-17 | Verfahren zur Herstellung von Cyclohexanon durch selektive Hydrierung von Phenol In der Gasphase |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU413656A3 true SU413656A3 (OSRAM) | 1974-01-30 |
Family
ID=5782627
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU1697505A SU413656A3 (OSRAM) | 1970-09-17 | 1971-09-15 |
Country Status (15)
| Country | Link |
|---|---|
| JP (1) | JPS528824B1 (OSRAM) |
| BE (1) | BE772764A (OSRAM) |
| BG (1) | BG21013A3 (OSRAM) |
| CA (1) | CA996953A (OSRAM) |
| CH (1) | CH558675A (OSRAM) |
| CS (1) | CS170103B2 (OSRAM) |
| ES (1) | ES395133A1 (OSRAM) |
| FR (1) | FR2108255A5 (OSRAM) |
| GB (1) | GB1368449A (OSRAM) |
| HU (1) | HU163988B (OSRAM) |
| IT (1) | IT954133B (OSRAM) |
| NL (1) | NL170726C (OSRAM) |
| PL (1) | PL77961B1 (OSRAM) |
| RO (1) | RO59280A (OSRAM) |
| SU (1) | SU413656A3 (OSRAM) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4272326A (en) * | 1980-01-24 | 1981-06-09 | Allied Chemical Corporation | Enhanced distillation of cyclohexanol from phenol with additional cyclohexanone feed |
| GB9306334D0 (en) * | 1993-03-26 | 1993-05-19 | Univ Dundee | Catalyst |
| WO2010005859A2 (en) * | 2008-07-07 | 2010-01-14 | Albemarle Corporation | Processes for hydrogenating aromatic amines |
-
1971
- 1971-09-09 HU HUBA2644A patent/HU163988B/hu unknown
- 1971-09-12 BG BG018534A patent/BG21013A3/xx unknown
- 1971-09-13 CS CS6518A patent/CS170103B2/cs unknown
- 1971-09-14 CA CA122,757A patent/CA996953A/en not_active Expired
- 1971-09-15 SU SU1697505A patent/SU413656A3/ru active
- 1971-09-15 IT IT28688/71A patent/IT954133B/it active
- 1971-09-16 CH CH1361071A patent/CH558675A/xx not_active IP Right Cessation
- 1971-09-16 PL PL1971150526A patent/PL77961B1/pl unknown
- 1971-09-16 GB GB4325171A patent/GB1368449A/en not_active Expired
- 1971-09-16 ES ES395133A patent/ES395133A1/es not_active Expired
- 1971-09-16 JP JP46071305A patent/JPS528824B1/ja active Pending
- 1971-09-16 NL NLAANVRAGE7112756,A patent/NL170726C/xx not_active IP Right Cessation
- 1971-09-17 BE BE772764A patent/BE772764A/xx not_active IP Right Cessation
- 1971-09-17 FR FR7133606A patent/FR2108255A5/fr not_active Expired
- 1971-09-17 RO RO68226A patent/RO59280A/ro unknown
Also Published As
| Publication number | Publication date |
|---|---|
| GB1368449A (en) | 1974-09-25 |
| ES395133A1 (es) | 1974-11-16 |
| HU163988B (OSRAM) | 1973-12-28 |
| CA996953A (en) | 1976-09-14 |
| FR2108255A5 (OSRAM) | 1972-05-19 |
| IT954133B (it) | 1973-08-30 |
| BG21013A3 (bg) | 1976-01-20 |
| CS170103B2 (OSRAM) | 1976-08-27 |
| CH558675A (de) | 1975-02-14 |
| NL170726B (nl) | 1982-07-16 |
| NL170726C (nl) | 1982-12-16 |
| PL77961B1 (OSRAM) | 1975-04-30 |
| DE2045882B2 (de) | 1976-01-15 |
| BE772764A (OSRAM) | 1972-03-17 |
| DE2045882A1 (de) | 1972-03-23 |
| JPS528824B1 (OSRAM) | 1977-03-11 |
| NL7112756A (OSRAM) | 1972-03-21 |
| RO59280A (OSRAM) | 1976-02-15 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE69615514T2 (de) | Selektive Hydrierungskatalysator und Verfahren unter Verwendung derselben | |
| US3932514A (en) | Catalyst for the preparation of cyclohexanone from phenol and process therefor | |
| KR0160308B1 (ko) | 시클로 올레핀의 제조법 | |
| US3534110A (en) | Production of phenol by the catalytic dehydrogenation of cyclohexanol and/or cyclohexanone | |
| EP0234745A1 (en) | Catalysts | |
| US4691070A (en) | Catalyst, its method of preparation and process for its use in the hydrogenation of diolefins | |
| KR100258903B1 (ko) | 은 함유 산화알루미늄 촉매 및 질소산화물의 분해방법 | |
| US3514492A (en) | Dehydrogenation catalyst and a process for dehydrogenating cyclic alcohols and ketones | |
| CN100387521C (zh) | 氨合成用催化剂 | |
| JPH0376789A (ja) | 液状炭化水素中の砒素および燐除去用の捕集物質、その製造方法およびその使用法 | |
| US4360504A (en) | Simultaneous destruction of trace components in the reaction off-gas from the synthesis of melamine | |
| SU413656A3 (OSRAM) | ||
| DE19937105A1 (de) | Oxidkatalysatoren | |
| DE68902022T2 (de) | Verfahren zur hydrogenierung von 1,1,2-trichloro-1,2,2-trifluoroethan. | |
| TW200848160A (en) | A dehydrogenation catalyst, process for preparation, and a method of use thereof | |
| JPS6123175B2 (OSRAM) | ||
| KR920007593B1 (ko) | 메탄올의 분해방법 | |
| CZ291458B6 (cs) | Způsob dehydrogenace sekundárních cyklických alkoholů, dehydrogenační katalyzátor, způsob jeho výroby a použití | |
| JPS59204145A (ja) | カルボニル化合物の製造方法 | |
| JPS6256788B2 (OSRAM) | ||
| JPH0247972B2 (OSRAM) | ||
| KR0131932B1 (ko) | 시클로헥사놀의 탈수소화반응에 의한 시클로헥사논 제조용 촉매 및 이의 제조방법 | |
| DE4132944A1 (de) | Verfahren zur herstellung von hydroxydiphenylen | |
| JPH02202855A (ja) | 第2級アミンの製造方法 | |
| US3875080A (en) | Process for preparing supported silver catalysts for the production of ethylene oxide |