DD216447A5 - Verfahren zur herstellung von methanol - Google Patents
Verfahren zur herstellung von methanol Download PDFInfo
- Publication number
- DD216447A5 DD216447A5 DD83253921A DD25392183A DD216447A5 DD 216447 A5 DD216447 A5 DD 216447A5 DD 83253921 A DD83253921 A DD 83253921A DD 25392183 A DD25392183 A DD 25392183A DD 216447 A5 DD216447 A5 DD 216447A5
- Authority
- DD
- German Democratic Republic
- Prior art keywords
- surface area
- carbon
- effective
- catalyst
- methanol
- Prior art date
Links
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 title claims abstract description 114
- 238000002360 preparation method Methods 0.000 title description 6
- 239000003054 catalyst Substances 0.000 claims abstract description 93
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 64
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 60
- 238000004519 manufacturing process Methods 0.000 claims abstract description 21
- 238000000034 method Methods 0.000 claims abstract description 16
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 15
- 229910002091 carbon monoxide Inorganic materials 0.000 claims abstract description 10
- 230000008569 process Effects 0.000 claims abstract description 10
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims description 67
- 229910052763 palladium Inorganic materials 0.000 claims description 26
- 239000001257 hydrogen Substances 0.000 claims description 11
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 9
- 239000007864 aqueous solution Substances 0.000 claims description 7
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims description 6
- 150000004820 halides Chemical class 0.000 claims description 5
- -1 palladium halide Chemical class 0.000 claims description 3
- 230000000737 periodic effect Effects 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 3
- 229910052746 lanthanum Inorganic materials 0.000 claims description 2
- FZLIPJUXYLNCLC-UHFFFAOYSA-N lanthanum atom Chemical compound [La] FZLIPJUXYLNCLC-UHFFFAOYSA-N 0.000 claims 1
- 239000002585 base Substances 0.000 abstract description 16
- 229910052783 alkali metal Inorganic materials 0.000 abstract description 11
- 150000001340 alkali metals Chemical class 0.000 abstract description 11
- 229910052784 alkaline earth metal Inorganic materials 0.000 abstract description 4
- 150000001342 alkaline earth metals Chemical class 0.000 abstract description 4
- 229910052747 lanthanoid Inorganic materials 0.000 abstract description 4
- 150000002602 lanthanoids Chemical class 0.000 abstract description 4
- 230000000694 effects Effects 0.000 description 22
- 239000007789 gas Substances 0.000 description 20
- 238000006243 chemical reaction Methods 0.000 description 17
- 230000015572 biosynthetic process Effects 0.000 description 16
- 230000009467 reduction Effects 0.000 description 12
- 238000003786 synthesis reaction Methods 0.000 description 11
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 9
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- 150000001875 compounds Chemical class 0.000 description 7
- 229930195733 hydrocarbon Natural products 0.000 description 7
- 150000002430 hydrocarbons Chemical class 0.000 description 7
- 229910052751 metal Inorganic materials 0.000 description 7
- 239000002184 metal Substances 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 6
- 238000005470 impregnation Methods 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 239000008188 pellet Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 239000012298 atmosphere Substances 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 230000003647 oxidation Effects 0.000 description 5
- 238000007254 oxidation reaction Methods 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 229910004298 SiO 2 Inorganic materials 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 229910052700 potassium Inorganic materials 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 3
- 239000000969 carrier Substances 0.000 description 3
- 238000006555 catalytic reaction Methods 0.000 description 3
- 239000003245 coal Substances 0.000 description 3
- 238000001704 evaporation Methods 0.000 description 3
- 229910002804 graphite Inorganic materials 0.000 description 3
- 239000010439 graphite Substances 0.000 description 3
- 150000002941 palladium compounds Chemical class 0.000 description 3
- 239000000741 silica gel Substances 0.000 description 3
- 229910002027 silica gel Inorganic materials 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 238000001179 sorption measurement Methods 0.000 description 3
- 239000007858 starting material Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- 235000019241 carbon black Nutrition 0.000 description 2
- 238000006356 dehydrogenation reaction Methods 0.000 description 2
- QHMGJGNTMQDRQA-UHFFFAOYSA-N dotriacontane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC QHMGJGNTMQDRQA-UHFFFAOYSA-N 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 239000010419 fine particle Substances 0.000 description 2
- 150000002431 hydrogen Chemical class 0.000 description 2
- 238000010348 incorporation Methods 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 239000002574 poison Substances 0.000 description 2
- 231100000614 poison Toxicity 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- VEUMANXWQDHAJV-UHFFFAOYSA-N 2-[2-[(2-hydroxyphenyl)methylideneamino]ethyliminomethyl]phenol Chemical compound OC1=CC=CC=C1C=NCCN=CC1=CC=CC=C1O VEUMANXWQDHAJV-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 229910052684 Cerium Inorganic materials 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 1
- 241001474977 Palla Species 0.000 description 1
- 108010013381 Porins Proteins 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 241000282887 Suidae Species 0.000 description 1
- 238000002441 X-ray diffraction Methods 0.000 description 1
- 229910052769 Ytterbium Inorganic materials 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000003929 acidic solution Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 150000001540 azides Chemical class 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 229910052790 beryllium Inorganic materials 0.000 description 1
- ATBAMAFKBVZNFJ-UHFFFAOYSA-N beryllium atom Chemical compound [Be] ATBAMAFKBVZNFJ-UHFFFAOYSA-N 0.000 description 1
- 238000003339 best practice Methods 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 229910052792 caesium Inorganic materials 0.000 description 1
- 239000003990 capacitor Substances 0.000 description 1
- 150000001721 carbon Chemical class 0.000 description 1
- 239000011203 carbon fibre reinforced carbon Substances 0.000 description 1
- 239000012876 carrier material Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 150000003841 chloride salts Chemical class 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- MCWXGJITAZMZEV-UHFFFAOYSA-N dimethoate Chemical compound CNC(=O)CSP(=S)(OC)OC MCWXGJITAZMZEV-UHFFFAOYSA-N 0.000 description 1
- 229910001882 dioxygen Inorganic materials 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000003344 environmental pollutant Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical class [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 210000004072 lung Anatomy 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000003415 peat Substances 0.000 description 1
- 150000003018 phosphorus compounds Chemical class 0.000 description 1
- 231100000719 pollutant Toxicity 0.000 description 1
- 102000007739 porin activity proteins Human genes 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 229910052702 rhenium Inorganic materials 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- 239000010948 rhodium Substances 0.000 description 1
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 230000004580 weight loss Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C31/00—Saturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
- C07C31/02—Monohydroxylic acyclic alcohols
- C07C31/04—Methanol
-
- 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
- B01J23/63—Platinum group metals with rare earths or actinides
-
- 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
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/15—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of oxides of carbon exclusively
- C07C29/151—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of oxides of carbon exclusively with hydrogen or hydrogen-containing gases
- C07C29/153—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of oxides of carbon exclusively with hydrogen or hydrogen-containing gases characterised by the catalyst used
- C07C29/156—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of oxides of carbon exclusively with hydrogen or hydrogen-containing gases characterised by the catalyst used containing iron group metals, platinum group metals or compounds thereof
- C07C29/157—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of oxides of carbon exclusively with hydrogen or hydrogen-containing gases characterised by the catalyst used containing iron group metals, platinum group metals or compounds thereof containing platinum group metals or compounds thereof
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
- Hydrogen, Water And Hydrids (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB8223453 | 1982-08-14 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DD216447A5 true DD216447A5 (de) | 1984-12-12 |
Family
ID=10532315
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD83253921A DD216447A5 (de) | 1982-08-14 | 1983-08-12 | Verfahren zur herstellung von methanol |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US4476250A (fr) |
| EP (1) | EP0101645B1 (fr) |
| JP (1) | JPS5948426A (fr) |
| KR (1) | KR840005999A (fr) |
| AU (1) | AU554395B2 (fr) |
| BR (1) | BR8307482A (fr) |
| CA (1) | CA1200561A (fr) |
| DD (1) | DD216447A5 (fr) |
| DE (1) | DE3361071D1 (fr) |
| DK (1) | DK369583A (fr) |
| ES (1) | ES524926A0 (fr) |
| GB (1) | GB2125400B (fr) |
| NO (1) | NO832891L (fr) |
| PL (1) | PL243411A1 (fr) |
| WO (1) | WO1984000749A1 (fr) |
| ZA (1) | ZA835809B (fr) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB8321255D0 (en) * | 1983-08-06 | 1983-09-07 | British Petroleum Co Plc | Methanol conversion process |
| JPS60195079A (ja) * | 1984-03-14 | 1985-10-03 | 日立化成工業株式会社 | パワ−モジユ−ル基板及びその製造方法 |
| FR2565126A1 (fr) * | 1984-05-30 | 1985-12-06 | Applic Catalytiques Ste Ly | Nouvelle composition catalytique pour la combustion d'hydrocarbures et plus particulierement du methane |
| JPS61143332A (ja) * | 1984-12-18 | 1986-07-01 | Agency Of Ind Science & Technol | 含酸素化合物の合成法 |
| US5427762A (en) * | 1987-05-27 | 1995-06-27 | Hydrocarb Corporation | Process for the conversion of carbonaceous feedstocks to particulate carbon and methanol |
| ZA908290B (en) * | 1989-10-20 | 1991-09-25 | Hydrocarb Corp | Process for the conversion of carbonaceous feedstocks to particulate carbon and methanol |
| US7456327B2 (en) | 2004-07-29 | 2008-11-25 | Gas Technologies, Llc | Method for direct-oxygenation of alkane gases |
| US8202916B2 (en) * | 2004-07-29 | 2012-06-19 | Gas Technologies Llc | Method of and apparatus for producing methanol |
| US7642293B2 (en) * | 2004-07-29 | 2010-01-05 | Gas Technologies Llc | Method and apparatus for producing methanol with hydrocarbon recycling |
| US8293186B2 (en) * | 2004-07-29 | 2012-10-23 | Gas Technologies Llc | Method and apparatus for producing methanol |
| US9180426B2 (en) * | 2004-07-29 | 2015-11-10 | Gas Technologies, Llc | Scrubber for methanol production system |
| US7910787B2 (en) | 2004-07-29 | 2011-03-22 | Gas Technologies Llc | Method and system for methanol production |
| US7578981B2 (en) * | 2004-07-29 | 2009-08-25 | Gas Technologies Llc | System for direct-oxygenation of alkane gases |
| US7879296B2 (en) * | 2005-12-27 | 2011-02-01 | Gas Technologies Llc | Tandem reactor system having an injectively-mixed backmixing reaction chamber, tubular-reactor, and axially movable interface |
| US7687669B2 (en) | 2005-12-27 | 2010-03-30 | Gas Technologies Llc | Method for direct-oxygenation of alkane gases |
| US20080260631A1 (en) | 2007-04-18 | 2008-10-23 | H2Gen Innovations, Inc. | Hydrogen production process |
| JP5662044B2 (ja) * | 2010-03-31 | 2015-01-28 | 大阪瓦斯株式会社 | 触媒の活性化の程度を判定する方法 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1397293A (en) * | 1972-09-01 | 1975-06-11 | British Petroleum Co | Platinum group metal catalysts and their use |
| FR2282940A1 (fr) * | 1974-09-02 | 1976-03-26 | British Petroleum Co | Catalyseur d'un metal du groupe du platine et son support |
| JPS5271406A (en) * | 1975-12-08 | 1977-06-14 | Union Carbide Corp | Method of producing hydroxylated compound from synthesis gas by paladium catalyst |
| IT1085879B (it) * | 1976-04-08 | 1985-05-28 | Basf Ag | Processo per la preparazione di chetoni superiori |
| US4289710A (en) * | 1979-12-19 | 1981-09-15 | Union Carbide Corporation | Process for producing methanol from synthesis gas with palladium-calcium catalysts |
| US4289709A (en) * | 1979-12-19 | 1981-09-15 | Union Carbide Corporation | Preparation of methanol from synthesis gas with promoted palladium catalysts |
-
1983
- 1983-08-08 ZA ZA835809A patent/ZA835809B/xx unknown
- 1983-08-08 AU AU17670/83A patent/AU554395B2/en not_active Ceased
- 1983-08-10 CA CA000434266A patent/CA1200561A/fr not_active Expired
- 1983-08-11 BR BR8307482A patent/BR8307482A/pt unknown
- 1983-08-11 EP EP83304646A patent/EP0101645B1/fr not_active Expired
- 1983-08-11 GB GB08321678A patent/GB2125400B/en not_active Expired
- 1983-08-11 DE DE8383304646T patent/DE3361071D1/de not_active Expired
- 1983-08-11 NO NO832891A patent/NO832891L/no unknown
- 1983-08-11 WO PCT/GB1983/000201 patent/WO1984000749A1/fr unknown
- 1983-08-12 US US06/522,740 patent/US4476250A/en not_active Expired - Fee Related
- 1983-08-12 DD DD83253921A patent/DD216447A5/de unknown
- 1983-08-12 ES ES524926A patent/ES524926A0/es active Granted
- 1983-08-12 PL PL24341183A patent/PL243411A1/xx unknown
- 1983-08-12 JP JP58146738A patent/JPS5948426A/ja active Pending
- 1983-08-12 DK DK369583A patent/DK369583A/da unknown
- 1983-08-13 KR KR1019830003799A patent/KR840005999A/ko not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| KR840005999A (ko) | 1984-11-21 |
| GB8321678D0 (en) | 1983-09-14 |
| PL243411A1 (en) | 1984-07-30 |
| ES8600185A1 (es) | 1985-10-01 |
| AU554395B2 (en) | 1986-08-21 |
| US4476250A (en) | 1984-10-09 |
| DE3361071D1 (en) | 1985-11-28 |
| EP0101645A1 (fr) | 1984-02-29 |
| CA1200561A (fr) | 1986-02-11 |
| ES524926A0 (es) | 1985-10-01 |
| DK369583D0 (da) | 1983-08-12 |
| AU1767083A (en) | 1984-02-16 |
| DK369583A (da) | 1984-02-15 |
| EP0101645B1 (fr) | 1985-10-23 |
| NO832891L (no) | 1984-02-15 |
| JPS5948426A (ja) | 1984-03-19 |
| GB2125400B (en) | 1986-03-19 |
| WO1984000749A1 (fr) | 1984-03-01 |
| BR8307482A (pt) | 1984-08-14 |
| GB2125400A (en) | 1984-03-07 |
| ZA835809B (en) | 1985-03-27 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DD216447A5 (de) | Verfahren zur herstellung von methanol | |
| DE2748097C3 (de) | Verfahren zur herstellung von primaeren, gesaettigten und geradkettigen alkoholen | |
| DE69920379T2 (de) | Palladium-Ceroxid-Trägerkatalysator und Verfahren zur Herstellung von Methanol | |
| DE1470700B2 (de) | Verfahren zur Herstellung von Kraftgasen mit hohem Methangehalt | |
| DD218281A5 (de) | Verfahren zur herstellung eines fuer die ammoniakerzeugung geeigneten katalysators | |
| DE10393935T5 (de) | Fischer-Tropsch-Katalysatoren auf Eisen-Basis und Herstellungs- und Anwendungsverfahren | |
| DE3837308A1 (de) | Kupferhaltiger katalysator zur tieftemperaturkonvertierung | |
| DE4301470A1 (de) | Verfahren zur katalytischen Zersetzung von reinem oder in Gasgemischen enthaltenem Distickstoffmonoxid | |
| DE4310053A1 (de) | Hydrierkatalysator, ein Verfahren zur Herstellung und Verwendung | |
| DE2606755A1 (de) | Methanisierungs-traegerkatalysator | |
| DE3021878A1 (de) | Verfahren zur herstellung von aethylenglycol durch katalytische hydrierung | |
| DE19757297A1 (de) | Verfahren zur Herstellung oxidischer Katalysatoren, die Kupfer in einer Oxidationsstufe > 0 enthalten | |
| EP2070898B1 (fr) | Catalyseur d'oxychloration | |
| EP0761630B1 (fr) | Procédé de préparation d'alkylphénols | |
| DE2624396C2 (fr) | ||
| DE2538533C2 (de) | Verfahren zur Herstellung von Monoolefinen aus Paraffinen mit Kettenlängen von etwa 8 bis 24 Kohlenstoffatomen | |
| DE4292694C2 (de) | Katalysator, dessen Herstellung und dessen Verwendung zur Hydrierung von gasförmigem CO¶2¶ | |
| DE3315149A1 (de) | Selektive olefinsynthese mit hilfe von rutheniumkatalysatoren auf ceroxidhaltigen traegern | |
| DE2915395C2 (de) | Verfahren zur Herstellung eines Salzes der Brenztraubensäure | |
| DE3717111C2 (de) | Kupferoxid, Zinkoxid und Aluminiumoxid enthaltender Katalysator zur Tieftemperaturkonvertierung | |
| DE2362955A1 (de) | Verbessertes verfahren zur herstellung von kohlenwasserstoff-umwandlungskatalysatoren und deren verwendung | |
| DE3037047C2 (fr) | ||
| DE69926151T2 (de) | Kobalt-alumina-katalysatoren mit verbesserter aktivität für fischer-tropsch-synthese | |
| AT522823B1 (de) | Verfahren zur Herstellung von Kohlenstoffmonoxid | |
| DE102007029201A1 (de) | Kolloidaler Nanokatalysator und Verfahren zu dessen Herstellung |