CZ162093A3 - Process for preparing alcohols - Google Patents
Process for preparing alcohols Download PDFInfo
- Publication number
- CZ162093A3 CZ162093A3 CS931620A CS162093A CZ162093A3 CZ 162093 A3 CZ162093 A3 CZ 162093A3 CS 931620 A CS931620 A CS 931620A CS 162093 A CS162093 A CS 162093A CZ 162093 A3 CZ162093 A3 CZ 162093A3
- Authority
- CZ
- Czechia
- Prior art keywords
- butene
- process according
- catalyst
- olefin
- fraction
- Prior art date
Links
- 150000001298 alcohols Chemical class 0.000 title description 6
- 238000004519 manufacturing process Methods 0.000 title description 6
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 claims abstract description 48
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 claims abstract description 44
- 238000006243 chemical reaction Methods 0.000 claims abstract description 38
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 claims abstract description 13
- 230000003197 catalytic effect Effects 0.000 claims abstract description 5
- 239000003054 catalyst Substances 0.000 claims description 31
- 238000000034 method Methods 0.000 claims description 31
- 150000001336 alkenes Chemical class 0.000 claims description 30
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 28
- QQONPFPTGQHPMA-UHFFFAOYSA-N Propene Chemical compound CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 27
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical compound CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 claims description 24
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 18
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 14
- 239000000203 mixture Substances 0.000 claims description 13
- 239000007787 solid Substances 0.000 claims description 13
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 12
- 230000000694 effects Effects 0.000 claims description 9
- 238000005984 hydrogenation reaction Methods 0.000 claims description 7
- 238000002360 preparation method Methods 0.000 claims description 7
- 150000002148 esters Chemical class 0.000 claims description 6
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 claims description 6
- 229920000642 polymer Polymers 0.000 claims description 6
- 238000006384 oligomerization reaction Methods 0.000 claims description 5
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical group CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 claims description 4
- 239000003085 diluting agent Substances 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 3
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 2
- 229920001519 homopolymer Polymers 0.000 claims description 2
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 claims description 2
- 239000001294 propane Substances 0.000 claims description 2
- 229930195734 saturated hydrocarbon Natural products 0.000 claims description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 claims 2
- 239000001273 butane Substances 0.000 claims 1
- 230000000447 dimerizing effect Effects 0.000 claims 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 claims 1
- 238000006471 dimerization reaction Methods 0.000 abstract description 6
- ZWRUINPWMLAQRD-UHFFFAOYSA-N nonan-1-ol Chemical compound CCCCCCCCCO ZWRUINPWMLAQRD-UHFFFAOYSA-N 0.000 abstract description 6
- 239000000047 product Substances 0.000 description 25
- 239000004014 plasticizer Substances 0.000 description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- XNMQEEKYCVKGBD-UHFFFAOYSA-N dimethylacetylene Natural products CC#CC XNMQEEKYCVKGBD-UHFFFAOYSA-N 0.000 description 5
- -1 nonyl alcohols Chemical class 0.000 description 5
- 238000006116 polymerization reaction Methods 0.000 description 5
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 5
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 230000007423 decrease Effects 0.000 description 4
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 239000005909 Kieselgur Substances 0.000 description 3
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 3
- DROMNWUQASBTFM-UHFFFAOYSA-N dinonyl benzene-1,2-dicarboxylate Chemical compound CCCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCCC DROMNWUQASBTFM-UHFFFAOYSA-N 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 230000029936 alkylation Effects 0.000 description 2
- 238000005804 alkylation reaction Methods 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 229910017052 cobalt Inorganic materials 0.000 description 2
- 239000010941 cobalt Substances 0.000 description 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 150000001993 dienes Chemical class 0.000 description 2
- HBGGXOJOCNVPFY-UHFFFAOYSA-N diisononyl phthalate Chemical compound CC(C)CCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCC(C)C HBGGXOJOCNVPFY-UHFFFAOYSA-N 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 238000006385 ozonation reaction Methods 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- MRMOZBOQVYRSEM-UHFFFAOYSA-N tetraethyllead Chemical compound CC[Pb](CC)(CC)CC MRMOZBOQVYRSEM-UHFFFAOYSA-N 0.000 description 2
- ZGEGCLOFRBLKSE-UHFFFAOYSA-N 1-Heptene Chemical class CCCCCC=C ZGEGCLOFRBLKSE-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Chemical class CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
- NHTMVDHEPJAVLT-UHFFFAOYSA-N Isooctane Chemical compound CC(C)CC(C)(C)C NHTMVDHEPJAVLT-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 1
- 229920012485 Plasticized Polyvinyl chloride Polymers 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 229910021536 Zeolite Inorganic materials 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 125000003158 alcohol group Chemical group 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 235000013844 butane Nutrition 0.000 description 1
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 239000007810 chemical reaction solvent Substances 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 125000005442 diisocyanate group Chemical group 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 235000011180 diphosphates Nutrition 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 238000007037 hydroformylation reaction Methods 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- DUUPDCPVCHSTFF-UHFFFAOYSA-N nonane Chemical compound [CH2]CCCCCCCC DUUPDCPVCHSTFF-UHFFFAOYSA-N 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000002574 poison Substances 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920000137 polyphosphoric acid Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 235000015320 potassium carbonate Nutrition 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000008149 soap solution Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- ZCUFMDLYAMJYST-UHFFFAOYSA-N thorium dioxide Chemical compound O=[Th]=O ZCUFMDLYAMJYST-UHFFFAOYSA-N 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Classifications
-
- 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
- C07C29/16—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by oxo-reaction combined with reduction
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB919102513A GB9102513D0 (en) | 1991-02-06 | 1991-02-06 | Hydrocarbon production |
| PCT/EP1992/000245 WO1992013818A1 (en) | 1991-02-06 | 1992-02-04 | Alcohol production |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CZ162093A3 true CZ162093A3 (en) | 1994-02-16 |
Family
ID=10689613
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CS931620A CZ162093A3 (en) | 1991-02-06 | 1992-02-04 | Process for preparing alcohols |
Country Status (17)
| Country | Link |
|---|---|
| EP (1) | EP0570411B1 (OSRAM) |
| JP (1) | JPH06504994A (OSRAM) |
| KR (1) | KR930703225A (OSRAM) |
| AT (1) | ATE142190T1 (OSRAM) |
| AU (1) | AU661987B2 (OSRAM) |
| BR (1) | BR9205595A (OSRAM) |
| CA (1) | CA2103587C (OSRAM) |
| CZ (1) | CZ162093A3 (OSRAM) |
| DE (1) | DE69213435T2 (OSRAM) |
| GB (1) | GB9102513D0 (OSRAM) |
| HU (1) | HUT64936A (OSRAM) |
| MY (1) | MY110784A (OSRAM) |
| RU (1) | RU2094420C1 (OSRAM) |
| SG (1) | SG43211A1 (OSRAM) |
| SK (1) | SK84293A3 (OSRAM) |
| TW (1) | TW213446B (OSRAM) |
| WO (1) | WO1992013818A1 (OSRAM) |
Families Citing this family (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE4221472A1 (de) * | 1992-06-30 | 1994-01-05 | Hoechst Ag | Gemische isomerer Decylalkohole, daraus erhältliche Phthalsäureester und ihre Verwendung als Weichmacher |
| DE19906518A1 (de) | 1999-02-17 | 2000-08-31 | Oxeno Olefinchemie Gmbh | Verfahren zur Fraktionierung von Dibuten |
| DE19908320A1 (de) * | 1999-02-26 | 2000-08-31 | Oxeno Olefinchemie Gmbh | Verfahren zur Herstellung von Vinylestern aus Butenoligomeren |
| AU778207B2 (en) * | 1999-04-21 | 2004-11-25 | Basf Aktiengesellschaft | Mixture of adipic or phthalic acid diesters and isomeric nonanols |
| EP1113034B1 (de) * | 1999-12-23 | 2001-09-12 | Basf Aktiengesellschaft | Mit isomeren Nonanolen abgeschlossene Polyester, Verfahren zu ihrer Herstellung und ihre Verwendung als Weichmacher |
| DE10003482A1 (de) * | 2000-01-27 | 2001-08-02 | Basf Ag | Verfahren zur Herstellung von C9-Alkoholen und Verfahren zur integrierten Herstellung von C9-Alkoholen und C10-Alkoholen |
| DE10135906A1 (de) | 2001-07-24 | 2003-02-06 | Oxeno Olefinchemie Gmbh | Verfahren zur Hydroformylierung von höheren Olefinen mit Kobaltverbindungen als Katalysator |
| EP1680388A1 (en) * | 2003-10-15 | 2006-07-19 | Shell International Research Maatschappij B.V. | Preparation of branched aliphatic alcohols using combined process streams from a hydrogenation unit and a dehydrogenation-isomerization unit |
| DE102004033410A1 (de) * | 2004-02-14 | 2005-09-01 | Oxeno Olefinchemie Gmbh | Verfahren zur Herstellung von Olefinen mit 8 bis 12 Kohlenstoffatomen |
| DE102004029732A1 (de) | 2004-06-21 | 2006-01-19 | Basf Ag | Hilfsmittel enthaltend Cyclohexanpolycarbonsäurederivate |
| DE602005008985D1 (de) | 2004-08-04 | 2008-09-25 | Exxonmobil Chem Patents Inc | Mischungen von c8-c10-alkoholen und davon abgeleitete weichmacher |
| DE102004059293A1 (de) | 2004-12-09 | 2006-06-14 | Oxeno Olefinchemie Gmbh | Verfahren zur Hydroformylierung von Olefinen |
| DE102004059292A1 (de) | 2004-12-09 | 2006-06-14 | Oxeno Olefinchemie Gmbh | Verfahren zur Herstellung von Alkoholen aus Olefinen durch Hydroformylierung und Hydrierung |
| TWI260798B (en) | 2005-05-02 | 2006-08-21 | Ind Tech Res Inst | Highly heat-dissipating light-emitting diode |
| DE102005021075A1 (de) | 2005-05-06 | 2006-11-09 | Oxeno Olefinchemie Gmbh | Verfahren zur Herstellung von Carbonsäureestern |
| DE102008007080A1 (de) | 2008-01-31 | 2009-08-06 | Evonik Oxeno Gmbh | Verfahren zur Herstellung von C9-Alkohol aus C8-Olefinen |
| PL2373716T3 (pl) | 2008-12-05 | 2014-01-31 | Basf Se | Pochodne kwasów cykloheksanopolikarboksylowych jako plastyfikatory do klejów i szczeliw |
| US8901344B2 (en) | 2008-12-16 | 2014-12-02 | Basf Se | Production of carboxylic acid esters by stripping with alcohol vapor |
| CN102256923B (zh) | 2008-12-16 | 2013-12-04 | 巴斯夫欧洲公司 | 制备羧酸酯的方法 |
| DE102009029284A1 (de) | 2009-09-08 | 2011-03-10 | Evonik Oxeno Gmbh | Verfahren zur Oligomerisierung von Olefinen |
| WO2011054781A1 (de) | 2009-11-03 | 2011-05-12 | Basf Se | THERMOPLASTISCHE ZUSAMMENSETZUNGEN MIT VERBESSERTER FLIEßFÄHIGKEIT |
| BR112012030589A2 (pt) | 2010-06-01 | 2016-08-16 | Basf Se | composição, processo para produzir composições poliméricas de estireno expansível, e um material de espuma, material de espuma, método para usar um material de espuma e um éster ciclo-hexanocarboxílico |
| WO2012078218A1 (en) | 2010-12-07 | 2012-06-14 | Exxonmobil Chemical Patents Inc. | Processes utilizing solvent extraction |
| WO2013013886A2 (en) | 2011-07-25 | 2013-01-31 | Exxonmobil Chemical Patents Inc. | Olefin oligomerization process |
| CN103796748B (zh) | 2011-07-25 | 2016-08-17 | 埃克森美孚化学专利公司 | 集成的腈毒物吸附及解吸系统 |
| US9573861B2 (en) | 2011-07-25 | 2017-02-21 | Exxonmobil Chemical Patents Inc. | Olefin oligomerization process |
| US9428427B2 (en) | 2011-07-25 | 2016-08-30 | Exxonmobil Chemical Patents Inc. | Process for nitrile removal from hydrocarbon feeds |
| WO2013013888A2 (en) | 2011-07-25 | 2013-01-31 | Exxonmobil Chemical Patents Inc. | Olefin oligomerization process |
| EP2716623A1 (de) | 2012-10-05 | 2014-04-09 | Basf Se | Verfahren zur Herstellung von Cyclohexanpolycarbonsäure-Derivaten mit geringem Nebenproduktanteil |
| DE102014200072A1 (de) | 2014-01-08 | 2015-07-09 | Evonik Industries Ag | Dimerisierung von Olefinen |
| JP2017526660A (ja) | 2014-08-01 | 2017-09-14 | ビーエーエスエフ ソシエタス・ヨーロピアＢａｓｆ Ｓｅ | エステル化触媒加水分解生成物を懸濁粒子形態で含む粗製エステルを後処理するための方法 |
| ZA201801183B (en) | 2017-02-27 | 2019-01-30 | Evonik Degussa Gmbh | Selective oligomerization of olefins |
| EP3931175B1 (de) | 2019-02-25 | 2024-04-10 | Basf Se | Verfahren zur aufarbeitung von benzolpolycarbonsäureestern und deren verwendung zur herstellung von cyclohexanpolycarbonsäureestern |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB477128A (en) * | 1936-10-16 | 1937-12-22 | Universal Oil Prod Co | Process for the manufacture of hydrocarbons suitable for use in motor fuel blends |
| IT1074653B (it) * | 1977-01-11 | 1985-04-20 | Euteco Spa | Procedimento per la produzione di olefine |
| US4123471A (en) * | 1977-07-26 | 1978-10-31 | Natale Bertolini | Olefin production process |
| JPS5847410B2 (ja) * | 1977-12-23 | 1983-10-22 | 日産化学工業株式会社 | 可塑剤組成物 |
| US4229586A (en) * | 1979-06-07 | 1980-10-21 | Uop Inc. | Process for production of motor fuel and phthalate esters or acyclic alcohols |
| US4675463A (en) * | 1986-02-05 | 1987-06-23 | Exxon Chemical Patents Inc. | Process for reducing fouling in higher olefin plants |
| DE3889936T2 (de) * | 1987-02-09 | 1995-01-26 | Mitsubishi Chem Ind | Alkoholgemisch für Plastifiziermittel. |
-
1991
- 1991-02-06 GB GB919102513A patent/GB9102513D0/en active Pending
-
1992
- 1992-01-31 MY MYPI92000169A patent/MY110784A/en unknown
- 1992-02-01 TW TW081100797A patent/TW213446B/zh active
- 1992-02-04 CA CA002103587A patent/CA2103587C/en not_active Expired - Fee Related
- 1992-02-04 EP EP92903627A patent/EP0570411B1/en not_active Expired - Lifetime
- 1992-02-04 CZ CS931620A patent/CZ162093A3/cs unknown
- 1992-02-04 WO PCT/EP1992/000245 patent/WO1992013818A1/en not_active Ceased
- 1992-02-04 AU AU11842/92A patent/AU661987B2/en not_active Ceased
- 1992-02-04 JP JP4503521A patent/JPH06504994A/ja active Pending
- 1992-02-04 AT AT92903627T patent/ATE142190T1/de not_active IP Right Cessation
- 1992-02-04 DE DE69213435T patent/DE69213435T2/de not_active Expired - Fee Related
- 1992-02-04 HU HU9302272A patent/HUT64936A/hu unknown
- 1992-02-04 KR KR1019930702326A patent/KR930703225A/ko not_active Ceased
- 1992-02-04 SK SK842-93A patent/SK84293A3/sk unknown
- 1992-02-04 SG SG1996005601A patent/SG43211A1/en unknown
- 1992-02-04 BR BR9205595A patent/BR9205595A/pt not_active Application Discontinuation
- 1992-02-04 RU RU9293051536A patent/RU2094420C1/ru active
Also Published As
| Publication number | Publication date |
|---|---|
| CA2103587C (en) | 2003-09-16 |
| AU1184292A (en) | 1992-09-07 |
| CA2103587A1 (en) | 1992-08-07 |
| GB9102513D0 (en) | 1991-03-27 |
| DE69213435T2 (de) | 1997-02-13 |
| HU9302272D0 (en) | 1993-11-29 |
| EP0570411A1 (en) | 1993-11-24 |
| SG43211A1 (en) | 1997-10-17 |
| BR9205595A (pt) | 1994-05-03 |
| JPH06504994A (ja) | 1994-06-09 |
| ATE142190T1 (de) | 1996-09-15 |
| WO1992013818A1 (en) | 1992-08-20 |
| KR930703225A (ko) | 1993-11-29 |
| DE69213435D1 (de) | 1996-10-10 |
| EP0570411B1 (en) | 1996-09-04 |
| HUT64936A (en) | 1994-03-28 |
| SK84293A3 (en) | 1994-04-06 |
| AU661987B2 (en) | 1995-08-17 |
| MY110784A (en) | 1999-04-30 |
| RU2094420C1 (ru) | 1997-10-27 |
| TW213446B (OSRAM) | 1993-09-21 |
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