GB1579159A - Manufacture of alkanols - Google Patents
Manufacture of alkanols Download PDFInfo
- Publication number
- GB1579159A GB1579159A GB26800/77A GB2680077A GB1579159A GB 1579159 A GB1579159 A GB 1579159A GB 26800/77 A GB26800/77 A GB 26800/77A GB 2680077 A GB2680077 A GB 2680077A GB 1579159 A GB1579159 A GB 1579159A
- Authority
- GB
- United Kingdom
- Prior art keywords
- weight
- alkanal
- alkanol
- carbon atoms
- catalyst
- 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
- 238000004519 manufacturing process Methods 0.000 title claims description 7
- 239000003054 catalyst Substances 0.000 claims description 27
- 238000000034 method Methods 0.000 claims description 23
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 19
- 125000004432 carbon atom Chemical group C* 0.000 claims description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
- 229910052759 nickel Inorganic materials 0.000 claims description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
- 239000006227 byproduct Substances 0.000 claims description 6
- 239000010949 copper Substances 0.000 claims description 6
- 238000007037 hydroformylation reaction Methods 0.000 claims description 6
- 229910052739 hydrogen Inorganic materials 0.000 claims description 6
- 239000001257 hydrogen Substances 0.000 claims description 6
- 239000011572 manganese Substances 0.000 claims description 6
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 claims description 5
- 239000002253 acid Substances 0.000 claims description 5
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 5
- 239000007791 liquid phase Substances 0.000 claims description 5
- 239000007858 starting material Substances 0.000 claims description 5
- 230000015572 biosynthetic process Effects 0.000 claims description 4
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 claims description 4
- 235000012239 silicon dioxide Nutrition 0.000 claims description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 3
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 claims description 3
- 150000001336 alkenes Chemical class 0.000 claims description 3
- 229910052802 copper Inorganic materials 0.000 claims description 3
- 229910052748 manganese Inorganic materials 0.000 claims description 3
- 239000000047 product Substances 0.000 claims description 3
- 238000000746 purification Methods 0.000 claims description 3
- QIDYONASNONTLI-UHFFFAOYSA-N 1,1-dipropoxypropane Chemical compound CCCOC(CC)OCCC QIDYONASNONTLI-UHFFFAOYSA-N 0.000 claims description 2
- PFNHSEQQEPMLNI-UHFFFAOYSA-N 2-methyl-1-pentanol Chemical compound CCCC(C)CO PFNHSEQQEPMLNI-UHFFFAOYSA-N 0.000 claims description 2
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 claims description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 2
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 2
- 238000003786 synthesis reaction Methods 0.000 claims description 2
- 238000005984 hydrogenation reaction Methods 0.000 description 13
- 229910052751 metal Inorganic materials 0.000 description 7
- 239000002184 metal Substances 0.000 description 7
- 229910002651 NO3 Inorganic materials 0.000 description 6
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 6
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 6
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N Butyraldehyde Chemical compound CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 description 5
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 5
- AMIMRNSIRUDHCM-UHFFFAOYSA-N Isopropylaldehyde Chemical compound CC(C)C=O AMIMRNSIRUDHCM-UHFFFAOYSA-N 0.000 description 4
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 150000001299 aldehydes Chemical class 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 238000004821 distillation Methods 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- NBBJYMSMWIIQGU-UHFFFAOYSA-N Propionic aldehyde Chemical compound CCC=O NBBJYMSMWIIQGU-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 238000010533 azeotropic distillation Methods 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 238000005470 impregnation Methods 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 1
- SZNYYWIUQFZLLT-UHFFFAOYSA-N 2-methyl-1-(2-methylpropoxy)propane Chemical compound CC(C)COCC(C)C SZNYYWIUQFZLLT-UHFFFAOYSA-N 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J177/00—Adhesives based on polyamides obtained by reactions forming a carboxylic amide link in the main chain; Adhesives based on derivatives of such polymers
-
- 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
- B01J23/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
- B01J23/76—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
- B01J23/84—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36 with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- B01J23/889—Manganese, technetium or rhenium
- B01J23/8892—Manganese
-
- 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
- C07C29/132—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 an oxygen containing functional group
- C07C29/136—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 an oxygen containing functional group of >C=O containing groups, e.g. —COOH
- C07C29/14—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 an oxygen containing functional group of >C=O containing groups, e.g. —COOH of a —CHO group
- C07C29/141—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 an oxygen containing functional group of >C=O containing groups, e.g. —COOH of a —CHO group with hydrogen or hydrogen-containing gases
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J123/00—Adhesives based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Adhesives based on derivatives of such polymers
- C09J123/02—Adhesives based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Adhesives based on derivatives of such polymers not modified by chemical after-treatment
- C09J123/04—Homopolymers or copolymers of ethene
- C09J123/08—Copolymers of ethene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
- C08L2666/02—Organic macromolecular compounds, natural resins, waxes or and bituminous materials
- C08L2666/04—Macromolecular compounds according to groups C08L7/00 - C08L49/00, or C08L55/00 - C08L57/00; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
- C08L2666/02—Organic macromolecular compounds, natural resins, waxes or and bituminous materials
- C08L2666/14—Macromolecular compounds according to C08L59/00 - C08L87/00; Derivatives thereof
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)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2628987A DE2628987C3 (de) | 1976-06-28 | 1976-06-28 | Verfahren zur Herstellung von C↓3↓-C↓5↓-Alkanolen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1579159A true GB1579159A (en) | 1980-11-12 |
Family
ID=5981652
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB26800/77A Expired GB1579159A (en) | 1976-06-28 | 1977-06-27 | Manufacture of alkanols |
Country Status (7)
| Country | Link |
|---|---|
| JP (1) | JPS532408A (enExample) |
| AT (1) | AT351005B (enExample) |
| CA (1) | CA1072123A (enExample) |
| DE (1) | DE2628987C3 (enExample) |
| ES (1) | ES460134A1 (enExample) |
| FR (1) | FR2356618A1 (enExample) |
| GB (1) | GB1579159A (enExample) |
Cited By (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1999029643A1 (en) * | 1997-12-11 | 1999-06-17 | Celanese International Corporation | Process for the production of n-propanol |
| US7321068B2 (en) | 2003-12-09 | 2008-01-22 | Basf Aktiengesellschaft | Method for producing tricyclodecandialdehyde |
| US7790937B2 (en) | 2006-03-03 | 2010-09-07 | Basf Se | Process for the preparation of 1,2-propanediol |
| US8252962B2 (en) | 2007-08-31 | 2012-08-28 | Basf Se | Method for producing 1,2-propandiol by hydrogenating glycerine in a two-step reactor cascade |
| US8273924B2 (en) | 2007-08-31 | 2012-09-25 | Basf Se | Method for producing 1,2-propandiol by low-pressure hydrogenation of glycerine |
| US8293951B2 (en) | 2007-08-31 | 2012-10-23 | Basf Se | Method for producing 1,2-propandiol by hydrogenation in at least three successive reactors |
| US8871985B2 (en) | 2010-03-15 | 2014-10-28 | Exxonmobil Chemical Patents Inc. | Processes for the production of alcohols |
| US9365715B2 (en) | 2010-12-23 | 2016-06-14 | Styrolution Europe Gmbh | Thermoplastic elastomer composition and method for the production thereof |
| US9567276B2 (en) | 2014-12-23 | 2017-02-14 | Evonik Degussa Gmbh | Chromium-free hydrogenation of hydroformylation mixtures |
| US10030120B2 (en) | 2013-12-06 | 2018-07-24 | Basf Se | Softener composition which contains tetrahydrofuran derivatives and 1,2-cyclohexane dicarboxylic acid esters |
| US10072133B2 (en) | 2014-01-09 | 2018-09-11 | Basf Se | Plasticizer composition containing furan derivatives and 1,2-cyclohexanedicarboxylic ester |
| US10266672B2 (en) | 2014-08-19 | 2019-04-23 | Basf Se | Plasticizer composition comprising polymeric dicarboxylic esters |
| US10273345B2 (en) | 2014-09-04 | 2019-04-30 | Basf Se | Plasticizer composition which contains a polymer dicarboxylic acid ester |
| US10287417B2 (en) | 2015-01-30 | 2019-05-14 | Basf Se | Plasticizer composition containing polymeric dicarboxylic acid esters and terephthalic acid dialkyl esters |
| US10287415B2 (en) | 2014-10-09 | 2019-05-14 | Basf Se | Plasticizer composition which comprises cycloalkyl esters of saturated dicarboxylic acids and terephthalic esters |
| US10329402B2 (en) | 2014-10-09 | 2019-06-25 | Basf Se | Plasticizer composition which comprises cycloalkyl esters of saturated dicarboxylic acids and 1,2-cyclohexanedicarboxylic esters |
| US10550242B2 (en) | 2016-01-20 | 2020-02-04 | Basf Se | Plasticiser composition containing aliphatic dicarboxylic acid esters and diesters selected from 1,2-cyclohexane dicarboxylic acid esters and terephthalic acid esters |
| US10787565B2 (en) | 2016-03-23 | 2020-09-29 | Basf Se | Polymer composition containing a cycloalkyl alkyl dicarboxylic acid diester as a plasticizer |
| US11014863B2 (en) | 2017-05-16 | 2021-05-25 | Basf Se | Hydroformylation method for the large-scale production of aldehydes and/or alcohols |
| US11591543B2 (en) | 2017-10-05 | 2023-02-28 | Basf Se | Aroma chemical compositions containing 3,5-diethyl-2-propyl-tetrahydropyran and/or unsaturated derivatives thereof |
Families Citing this family (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3228881C2 (de) * | 1982-08-03 | 1985-06-13 | Basf Ag, 6700 Ludwigshafen | Verfahren zur Herstellung von C↓3↓-C↓5↓-Alkoholen |
| CA1303412C (en) | 1985-05-31 | 1992-06-16 | Shigeharu Koboshi | Method for forming direct positive color image |
| DE10024542A1 (de) | 2000-05-18 | 2001-11-22 | Basf Ag | Verfahren zur Herstellung von gesättigten C3-C20-Alkoholen |
| WO2011009936A2 (en) | 2009-07-24 | 2011-01-27 | Basf Se | Process for the preparation of 1,2-propanediol from glycerol |
| MY185096A (en) | 2012-03-07 | 2021-04-30 | Basf Se | Method for thermal integration in the hydrogenation and distillation of c3-c20 aldehydes |
| US9035110B2 (en) | 2012-03-07 | 2015-05-19 | Basf Se | Process for heat integration in the hydrogenation and distillation of C3—C20-aldehydes |
| TWI654177B (zh) | 2013-10-31 | 2019-03-21 | 德商巴斯夫歐洲公司 | 製備羧酸酯的方法及其作爲塑化劑的用途 |
| CN106232571B (zh) | 2014-04-22 | 2019-05-28 | 巴斯夫欧洲公司 | 在离子液体和酸性酯化催化剂的存在下制备羧酸酯的方法及其作为塑化剂的用途 |
| DE102015207291A1 (de) | 2014-04-24 | 2016-03-10 | Basf Se | Weichmacher-Zusammensetzung, die Furanderivate und 1,2-Cyclohexandicarbonsäureester enthält |
| TW201605945A (zh) | 2014-07-08 | 2016-02-16 | 巴斯夫歐洲公司 | 包含二羧酸的酯及１，２－環己烷二羧酸的酯之模製化合物 |
| TW201609628A (zh) | 2014-07-08 | 2016-03-16 | 巴斯夫歐洲公司 | 包含脂族二羧酸二酯及對苯二甲酸二烷基酯之塑化劑組成物 |
| CA2999933A1 (en) | 2015-09-30 | 2017-04-06 | Basf Se | Plasticizer composition containing polymeric dicarboxylic acid esters and terephthalic acid dialkyl esters |
| WO2017055429A1 (de) | 2015-09-30 | 2017-04-06 | Basf Se | Weichmacher-zusammensetzung, die polymere dicarbonsäureester und 1,2-cyclohexandicarbonsäureester enthält |
| WO2017055431A1 (de) | 2015-09-30 | 2017-04-06 | Basf Se | Weichmacher-zusammensetzung, die polymere dicarbonsäureester und dicarbonsäurediester enthält |
| WO2018024597A1 (de) | 2016-08-01 | 2018-02-08 | Basf Se | Weichmacher-zusammensetzung |
| CN109563306A (zh) | 2016-08-01 | 2019-04-02 | 巴斯夫欧洲公司 | 增塑剂组合物 |
| WO2018024591A1 (de) | 2016-08-01 | 2018-02-08 | Basf Se | Weichmacher-zusammensetzung |
| WO2019185409A1 (de) | 2018-03-29 | 2019-10-03 | Basf Se | Pvc-zusammensetzung, enthaltend wenigstens einen weichmacher der wenigstens eine carbonsäureestergruppe aufweist und wenigstens eine carbodiimidverbindung |
| EP3747860B1 (de) | 2019-06-04 | 2023-07-26 | Basf Se | Neue weichmacher auf cyclohexanon-basis |
| EP3878831A1 (en) | 2020-03-10 | 2021-09-15 | Basf Se | Improved nickel-copper-manganese-catalyst for the preparation of alcohols by hydrogenation of the corresponding aldehydes and ketones |
| EP4249114A1 (en) | 2022-03-21 | 2023-09-27 | Basf Se | Nickel-copper-manganese hydrogenation catalyst comprising a silica support |
| WO2024133358A1 (de) | 2022-12-21 | 2024-06-27 | Basf Se | Weichmacher-verbindung |
| WO2024153687A1 (de) | 2023-01-19 | 2024-07-25 | Basf Se | Verfahren zur herstellung von 1,2-cyclohexandicarbonsäuredialkylestern |
| WO2024256670A1 (de) | 2023-06-15 | 2024-12-19 | Basf Se | Weichmacher-zusammensetzung |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1199194A (fr) * | 1957-07-16 | 1959-12-11 | Basf Ag | Procédé pour l'hydrogénation catalytique de composés carbocycliques à doubles liaisons oléfiniques |
| DE1276620B (de) * | 1965-11-26 | 1968-09-05 | Huels Chemische Werke Ag | Verfahren zur Herstellung von gesaettigten aliphatischen Alkoholen |
| FR1528522A (fr) * | 1966-06-25 | 1968-06-07 | Basf Ag | Procédé de préparation d'alcools saturés par hydrogénation d'aldéhydes ou de cétones |
| DE1269605B (de) * | 1966-06-25 | 1968-06-06 | Basf Ag | Verfahren zur Herstellung gesaettigter Alkohole durch Hydrieren von Aldehyden oder Ketonen |
| DE1277232B (de) * | 1967-03-18 | 1968-09-12 | Basf Ag | Verfahren zur Herstellung von gesaettigten aliphatischen Alkoholen |
| BE756877A (fr) * | 1969-09-30 | 1971-03-30 | Basf Ag | Procede de preparation du 2-ethylhexanol |
| US3950441A (en) * | 1970-09-16 | 1976-04-13 | Gaf Corporation | Process and catalyst for preparing 1,4-butanediol |
-
1976
- 1976-06-28 DE DE2628987A patent/DE2628987C3/de not_active Expired
-
1977
- 1977-05-25 CA CA279,113A patent/CA1072123A/en not_active Expired
- 1977-06-24 FR FR7719491A patent/FR2356618A1/fr active Granted
- 1977-06-27 GB GB26800/77A patent/GB1579159A/en not_active Expired
- 1977-06-27 ES ES460134A patent/ES460134A1/es not_active Expired
- 1977-06-27 AT AT452777A patent/AT351005B/de not_active IP Right Cessation
- 1977-06-28 JP JP7624277A patent/JPS532408A/ja active Pending
Cited By (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1999029643A1 (en) * | 1997-12-11 | 1999-06-17 | Celanese International Corporation | Process for the production of n-propanol |
| US7321068B2 (en) | 2003-12-09 | 2008-01-22 | Basf Aktiengesellschaft | Method for producing tricyclodecandialdehyde |
| US7790937B2 (en) | 2006-03-03 | 2010-09-07 | Basf Se | Process for the preparation of 1,2-propanediol |
| US8252962B2 (en) | 2007-08-31 | 2012-08-28 | Basf Se | Method for producing 1,2-propandiol by hydrogenating glycerine in a two-step reactor cascade |
| US8273924B2 (en) | 2007-08-31 | 2012-09-25 | Basf Se | Method for producing 1,2-propandiol by low-pressure hydrogenation of glycerine |
| US8293951B2 (en) | 2007-08-31 | 2012-10-23 | Basf Se | Method for producing 1,2-propandiol by hydrogenation in at least three successive reactors |
| US8871985B2 (en) | 2010-03-15 | 2014-10-28 | Exxonmobil Chemical Patents Inc. | Processes for the production of alcohols |
| US9365715B2 (en) | 2010-12-23 | 2016-06-14 | Styrolution Europe Gmbh | Thermoplastic elastomer composition and method for the production thereof |
| US10030120B2 (en) | 2013-12-06 | 2018-07-24 | Basf Se | Softener composition which contains tetrahydrofuran derivatives and 1,2-cyclohexane dicarboxylic acid esters |
| US10072133B2 (en) | 2014-01-09 | 2018-09-11 | Basf Se | Plasticizer composition containing furan derivatives and 1,2-cyclohexanedicarboxylic ester |
| US10266672B2 (en) | 2014-08-19 | 2019-04-23 | Basf Se | Plasticizer composition comprising polymeric dicarboxylic esters |
| US10273345B2 (en) | 2014-09-04 | 2019-04-30 | Basf Se | Plasticizer composition which contains a polymer dicarboxylic acid ester |
| US10287415B2 (en) | 2014-10-09 | 2019-05-14 | Basf Se | Plasticizer composition which comprises cycloalkyl esters of saturated dicarboxylic acids and terephthalic esters |
| US10329402B2 (en) | 2014-10-09 | 2019-06-25 | Basf Se | Plasticizer composition which comprises cycloalkyl esters of saturated dicarboxylic acids and 1,2-cyclohexanedicarboxylic esters |
| US9567276B2 (en) | 2014-12-23 | 2017-02-14 | Evonik Degussa Gmbh | Chromium-free hydrogenation of hydroformylation mixtures |
| US10287417B2 (en) | 2015-01-30 | 2019-05-14 | Basf Se | Plasticizer composition containing polymeric dicarboxylic acid esters and terephthalic acid dialkyl esters |
| US10550242B2 (en) | 2016-01-20 | 2020-02-04 | Basf Se | Plasticiser composition containing aliphatic dicarboxylic acid esters and diesters selected from 1,2-cyclohexane dicarboxylic acid esters and terephthalic acid esters |
| US10787565B2 (en) | 2016-03-23 | 2020-09-29 | Basf Se | Polymer composition containing a cycloalkyl alkyl dicarboxylic acid diester as a plasticizer |
| US11014863B2 (en) | 2017-05-16 | 2021-05-25 | Basf Se | Hydroformylation method for the large-scale production of aldehydes and/or alcohols |
| US11591543B2 (en) | 2017-10-05 | 2023-02-28 | Basf Se | Aroma chemical compositions containing 3,5-diethyl-2-propyl-tetrahydropyran and/or unsaturated derivatives thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| CA1072123A (en) | 1980-02-19 |
| ATA452777A (de) | 1978-12-15 |
| ES460134A1 (es) | 1978-10-01 |
| FR2356618A1 (fr) | 1978-01-27 |
| DE2628987B2 (de) | 1981-01-08 |
| DE2628987A1 (de) | 1978-01-12 |
| AT351005B (de) | 1979-07-10 |
| FR2356618B1 (enExample) | 1981-07-17 |
| JPS532408A (en) | 1978-01-11 |
| DE2628987C3 (de) | 1981-10-22 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| GB1579159A (en) | Manufacture of alkanols | |
| US6239318B1 (en) | Process for the selective hydrogenation of hydroformylation mixtures | |
| US2437600A (en) | Synthesis of aldehydes | |
| EP0269888B1 (en) | Aldehyde hydrogenation catalyst and process | |
| US2137407A (en) | Catalytic hydrogenation process | |
| US4876402A (en) | Improved aldehyde hydrogenation process | |
| EP0008767B1 (en) | A heterogeneous vapor phase process for the catalytic hydrogenation of aldehydes to alcohols | |
| US4749808A (en) | Proton-catalysed reactions in which water is not a stoichiometric reactant catalysed by metal cation exchanged layered clays | |
| US20110060169A1 (en) | Hydrogenation catalyst and process for preparing alcohols by hydrogenation of carbonyl compounds | |
| KR20000069794A (ko) | 다가 알콜의 제조 방법 | |
| CN104640829B (zh) | 新戊二醇的生产方法 | |
| DE2426108A1 (de) | Verfahren zur herstellung von methanol | |
| US2767221A (en) | Production of unsaturated alcohols | |
| US3248428A (en) | Aldolization process | |
| US3880940A (en) | Manufacture of aliphatic alcohols | |
| US2793236A (en) | Hydrogenation of oxo aldehyde bottoms | |
| US3991127A (en) | Production of saturated aliphatic alcohols | |
| US3361828A (en) | Preparation of higher molecular weight ketones | |
| US3501537A (en) | Process for separating high-boilers of the oxo process | |
| US2040913A (en) | Process for producing a tolyl carbinol | |
| EP0263462B1 (de) | Verfahren zur Herstellung von Aminen | |
| GB1570890A (en) | Process for producing tetrahydrofuran | |
| DE69204818T2 (de) | Verfahren zur Herstellung von Isobuten. | |
| US3272873A (en) | Hydrogenation of alpha, betaunsaturated aldehydes | |
| US5099073A (en) | Catalytic process for the production of diketone derivatives of polyoxypropylene glycols |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed | ||
| PE20 | Patent expired after termination of 20 years |
Effective date: 19970626 |