ZA200104830B - Isomerization process. - Google Patents

Isomerization process. Download PDF

Info

Publication number: ZA200104830B
Authority: ZA; South Africa
Prior art keywords: weight percent; internal olefins; olefins; product; double bond
Prior art date: 1999-11-04

Application number

ZA200104830A

Other languages

English (en)

Inventor

Fred Chun-Chien Twu

William L Cox

Original Assignee

Bp Corp North America Inc

Priority date (The priority date 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 date listed.)

1999-11-04

Filing date

2001-06-13

Publication date

2002-09-13

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=23721056&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=ZA200104830(B) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

2001-06-13 Application filed by Bp Corp North America Inc filed Critical Bp Corp North America Inc

2002-09-13 Publication of ZA200104830B publication Critical patent/ZA200104830B/en

Links

238000000034 method Methods 0.000 title claims description 41
238000006317 isomerization reaction Methods 0.000 title claims description 20
239000000203 mixture Substances 0.000 claims description 64
GGQQNYXPYWCUHG-RMTFUQJTSA-N (3e,6e)-deca-3,6-diene Chemical class CCC\C=C\C\C=C\CC GGQQNYXPYWCUHG-RMTFUQJTSA-N 0.000 claims description 45
150000001336 alkenes Chemical class 0.000 claims description 35
239000012530 fluid Substances 0.000 claims description 25
238000005553 drilling Methods 0.000 claims description 24
125000004432 carbon atom Chemical group C* 0.000 claims description 23
229910052799 carbon Inorganic materials 0.000 claims description 21
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 21
239000003054 catalyst Substances 0.000 claims description 19
PNEYBMLMFCGWSK-UHFFFAOYSA-N Alumina Chemical compound [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 16
229920002554 vinyl polymer Polymers 0.000 claims description 14
239000002199 base oil Substances 0.000 claims description 13
238000006243 chemical reaction Methods 0.000 claims description 12
239000002245 particle Substances 0.000 claims description 12
239000004711 α-olefin Substances 0.000 claims description 9
239000011148 porous material Substances 0.000 claims description 8
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 7
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 6
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 claims description 4
229910021529 ammonia Inorganic materials 0.000 claims description 3
239000007791 liquid phase Substances 0.000 claims description 3
239000011734 sodium Substances 0.000 claims description 3
229910052708 sodium Inorganic materials 0.000 claims description 3
239000011973 solid acid Substances 0.000 claims description 2
239000011949 solid catalyst Substances 0.000 claims 3
-1 vinylidene olefins Chemical class 0.000 description 20
150000001721 carbon Chemical group 0.000 description 12
239000003795 chemical substances by application Substances 0.000 description 8
GQEZCXVZFLOKMC-UHFFFAOYSA-N 1-hexadecene Chemical compound CCCCCCCCCCCCCCC=C GQEZCXVZFLOKMC-UHFFFAOYSA-N 0.000 description 7
239000000654 additive Substances 0.000 description 6
239000003995 emulsifying agent Substances 0.000 description 6
CCCMONHAUSKTEQ-UHFFFAOYSA-N octadec-1-ene Chemical compound CCCCCCCCCCCCCCCCC=C CCCMONHAUSKTEQ-UHFFFAOYSA-N 0.000 description 6
239000000080 wetting agent Substances 0.000 description 6
239000003921 oil Substances 0.000 description 4
239000000344 soap Substances 0.000 description 4
235000008733 Citrus aurantifolia Nutrition 0.000 description 3
235000011941 Tilia x europaea Nutrition 0.000 description 3
235000014113 dietary fatty acids Nutrition 0.000 description 3
239000000194 fatty acid Substances 0.000 description 3
229930195729 fatty acid Natural products 0.000 description 3
150000004665 fatty acids Chemical class 0.000 description 3
239000004571 lime Substances 0.000 description 3
AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical compound CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 2
CRSBERNSMYQZNG-UHFFFAOYSA-N 1-dodecene Chemical compound CCCCCCCCCCC=C CRSBERNSMYQZNG-UHFFFAOYSA-N 0.000 description 2
HFDVRLIODXPAHB-UHFFFAOYSA-N 1-tetradecene Chemical compound CCCCCCCCCCCCC=C HFDVRLIODXPAHB-UHFFFAOYSA-N 0.000 description 2
PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
230000000996 additive effect Effects 0.000 description 2
125000001931 aliphatic group Chemical group 0.000 description 2
239000000440 bentonite Substances 0.000 description 2
229910000278 bentonite Inorganic materials 0.000 description 2
SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
239000011575 calcium Substances 0.000 description 2
229910052791 calcium Inorganic materials 0.000 description 2
239000001110 calcium chloride Substances 0.000 description 2
229910001628 calcium chloride Inorganic materials 0.000 description 2
239000004927 clay Substances 0.000 description 2
238000006471 dimerization reaction Methods 0.000 description 2
238000006073 displacement reaction Methods 0.000 description 2
238000001914 filtration Methods 0.000 description 2
238000005755 formation reaction Methods 0.000 description 2
239000007789 gas Substances 0.000 description 2
239000003349 gelling agent Substances 0.000 description 2
DCAYPVUWAIABOU-UHFFFAOYSA-N hexadecane Chemical compound CCCCCCCCCCCCCCCC DCAYPVUWAIABOU-UHFFFAOYSA-N 0.000 description 2
239000007788 liquid Substances 0.000 description 2
VAMFXQBUQXONLZ-UHFFFAOYSA-N n-alpha-eicosene Natural products CCCCCCCCCCCCCCCCCCC=C VAMFXQBUQXONLZ-UHFFFAOYSA-N 0.000 description 2
RZJRJXONCZWCBN-UHFFFAOYSA-N octadecane Chemical compound CCCCCCCCCCCCCCCCCC RZJRJXONCZWCBN-UHFFFAOYSA-N 0.000 description 2
239000004033 plastic Substances 0.000 description 2
229920003023 plastic Polymers 0.000 description 2
239000007787 solid Substances 0.000 description 2
239000000725 suspension Substances 0.000 description 2
238000005303 weighing Methods 0.000 description 2
229940106006 1-eicosene Drugs 0.000 description 1
FIKTURVKRGQNQD-UHFFFAOYSA-N 1-eicosene Natural products CCCCCCCCCCCCCCCCCC=CC(O)=O FIKTURVKRGQNQD-UHFFFAOYSA-N 0.000 description 1
IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 1
QJZYHAIUNVAGQP-UHFFFAOYSA-N 3-nitrobicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic acid Chemical compound C1C2C=CC1C(C(=O)O)C2(C(O)=O)[N+]([O-])=O QJZYHAIUNVAGQP-UHFFFAOYSA-N 0.000 description 1
241000143060 Americamysis bahia Species 0.000 description 1
241000238557 Decapoda Species 0.000 description 1
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical group C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
239000005977 Ethylene Substances 0.000 description 1
239000004952 Polyamide Substances 0.000 description 1
229920002472 Starch Polymers 0.000 description 1
FHKPLLOSJHHKNU-INIZCTEOSA-N [(3S)-3-[8-(1-ethyl-5-methylpyrazol-4-yl)-9-methylpurin-6-yl]oxypyrrolidin-1-yl]-(oxan-4-yl)methanone Chemical compound C(C)N1N=CC(=C1C)C=1N(C2=NC=NC(=C2N=1)O[C@@H]1CN(CC1)C(=O)C1CCOCC1)C FHKPLLOSJHHKNU-INIZCTEOSA-N 0.000 description 1
239000002253 acid Substances 0.000 description 1
239000003377 acid catalyst Substances 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
231100000215 acute (single dose) toxicity testing Toxicity 0.000 description 1
238000011047 acute toxicity test Methods 0.000 description 1
230000032683 aging Effects 0.000 description 1
229910052782 aluminium Inorganic materials 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 1
239000010428 baryte Substances 0.000 description 1
229910052601 baryte Inorganic materials 0.000 description 1
GUBGYTABKSRVRQ-QRZGKKJRSA-N beta-cellobiose Chemical class OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O GUBGYTABKSRVRQ-QRZGKKJRSA-N 0.000 description 1
239000012267 brine Substances 0.000 description 1
239000011203 carbon fibre reinforced carbon Substances 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
238000005336 cracking Methods 0.000 description 1
238000005520 cutting process Methods 0.000 description 1
239000000539 dimer Substances 0.000 description 1
229940069096 dodecene Drugs 0.000 description 1
230000000694 effects Effects 0.000 description 1
IOZUKJFUMPAUNC-UHFFFAOYSA-N ethene triethylalumane Chemical group C=C.CC[Al](CC)CC IOZUKJFUMPAUNC-UHFFFAOYSA-N 0.000 description 1
125000000816 ethylene group Chemical class [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
229910052949 galena Inorganic materials 0.000 description 1
239000004021 humic acid Substances 0.000 description 1
238000011065 in-situ storage Methods 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 1
235000013980 iron oxide Nutrition 0.000 description 1
VBMVTYDPPZVILR-UHFFFAOYSA-N iron(2+);oxygen(2-) Chemical class [O-2].[Fe+2] VBMVTYDPPZVILR-UHFFFAOYSA-N 0.000 description 1
XCAUINMIESBTBL-UHFFFAOYSA-N lead(ii) sulfide Chemical compound [Pb]=S XCAUINMIESBTBL-UHFFFAOYSA-N 0.000 description 1
239000000787 lecithin Substances 0.000 description 1
229940067606 lecithin Drugs 0.000 description 1
235000010445 lecithin Nutrition 0.000 description 1
230000005012 migration Effects 0.000 description 1
238000013508 migration Methods 0.000 description 1
150000005673 monoalkenes Chemical group 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
150000002895 organic esters Chemical class 0.000 description 1
239000012071 phase Substances 0.000 description 1
230000000704 physical effect Effects 0.000 description 1
229920000058 polyacrylate Polymers 0.000 description 1
229920001281 polyalkylene Polymers 0.000 description 1
229920002647 polyamide Polymers 0.000 description 1
229920000768 polyamine Polymers 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
238000010926 purge Methods 0.000 description 1
150000003242 quaternary ammonium salts Chemical class 0.000 description 1
238000007086 side reaction Methods 0.000 description 1
229910021646 siderite Inorganic materials 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
FAPWRFPIFSIZLT-UHFFFAOYSA-M sodium chloride Inorganic materials [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
239000000243 solution Substances 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
235000019698 starch Nutrition 0.000 description 1
239000000126 substance Substances 0.000 description 1
150000005846 sugar alcohols Polymers 0.000 description 1
150000003871 sulfonates Chemical class 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
231100000419 toxicity Toxicity 0.000 description 1
230000001988 toxicity Effects 0.000 description 1
150000003626 triacylglycerols Chemical class 0.000 description 1
230000007306 turnover Effects 0.000 description 1
239000007762 w/o emulsion Substances 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
238000009736 wetting Methods 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
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K8/00—Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
- C09K8/02—Well-drilling compositions
- C09K8/32—Non-aqueous well-drilling compositions, e.g. oil-based
- C09K8/34—Organic liquids
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C11/00—Aliphatic unsaturated hydrocarbons
- C07C11/02—Alkenes
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C5/00—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
- C07C5/22—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by isomerisation
- C07C5/23—Rearrangement of carbon-to-carbon unsaturated bonds
- C07C5/25—Migration of carbon-to-carbon double bonds
- C07C5/2506—Catalytic processes
- C07C5/2512—Catalytic processes with metal oxides
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C5/00—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
- C07C5/22—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by isomerisation
- C07C5/27—Rearrangement of carbon atoms in the hydrocarbon skeleton
- C07C5/2767—Changing the number of side-chains
- C07C5/277—Catalytic processes
- C07C5/2772—Catalytic processes with metal oxides

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
General Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Life Sciences & Earth Sciences (AREA)
Oil, Petroleum & Natural Gas (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Lubricants (AREA)
Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Saccharide Compounds (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

ZA200104830A 1999-11-04 2001-06-13 Isomerization process. ZA200104830B (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US43366299A	1999-11-04	1999-11-04

Publications (1)

Publication Number	Publication Date
ZA200104830B true ZA200104830B (en)	2002-09-13

Family

ID=23721056

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
ZA200104830A ZA200104830B (en)	1999-11-04	2001-06-13	Isomerization process.

Country Status (13)

Country	Link
US (1)	US6407302B1 (fr)
EP (1)	EP1144349B2 (fr)
JP (1)	JP3771842B2 (fr)
AT (1)	ATE331700T1 (fr)
AU (1)	AU776570B2 (fr)
CA (1)	CA2358924C (fr)
CZ (1)	CZ303406B6 (fr)
DE (1)	DE60029086T3 (fr)
NO (1)	NO330309B1 (fr)
RU (1)	RU2241695C2 (fr)
TW (1)	TWI237013B (fr)
WO (1)	WO2001032590A2 (fr)
ZA (1)	ZA200104830B (fr)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR2811326B1 (fr) *	2000-07-05	2003-09-05	Inst Francais Du Petrole	Methode et fluide pour controler la saturation d'une formation aux abords d'un puits
US7078579B2 (en) *	2001-06-21	2006-07-18	Shell Oil Company	Process for the isomerization of a vinylidene olefin
US7041865B2 (en) *	2001-06-21	2006-05-09	Shell Oil Company	Process for the isomerization of an olefin
US7081437B2 (en) *	2003-08-25	2006-07-25	M-I L.L.C.	Environmentally compatible hydrocarbon blend drilling fluid
JP5173189B2 (ja) *	2003-09-26	2013-03-27	シエル・インターナシヨナル・リサーチ・マートスハツペイ・ベー・ヴエー	アルファオレフィンの異性化方法およびこれから得られる組成物
JP4764013B2 (ja) *	2005-01-12	2011-08-31	出光興産株式会社	内部オレフィンの製造方法、内部オレフィン混合物及び内部オレフィン混合物を含む石油掘削基油
US8748361B2 (en) *	2005-07-19	2014-06-10	Exxonmobil Chemical Patents Inc.	Polyalpha-olefin compositions and processes to produce the same
US20080261836A1 (en) *	2007-04-20	2008-10-23	Filler Paul A	Compositions for use in well servicing fluids
US8030248B2 (en) *	2009-06-15	2011-10-04	Ineos Usa Llc	Drilling fluid and process of making the same
US8356678B2 (en)	2010-10-29	2013-01-22	Racional Energy & Environment Company	Oil recovery method and apparatus
US9334436B2 (en) *	2010-10-29	2016-05-10	Racional Energy And Environment Company	Oil recovery method and product
US9234151B2 (en)	2011-10-10	2016-01-12	Exxonmobil Research And Engineering Company	Lubricating compositions
US9266793B2 (en)	2012-12-26	2016-02-23	Chevron Phillips Chemical Company Lp	Acid-catalyzed olefin oligomerizations
US20140275664A1 (en)	2013-03-13	2014-09-18	Chevron Phillips Chemical Company Lp	Processes for Preparing Low Viscosity Lubricants
HUE054256T2 (hu)	2013-11-20	2021-08-30	Lummus Technology Inc	Katalizátormérgeknek jól ellenálló, kettõs kötésû olefin-izomerizációs katalizátor
US9708549B2 (en)	2013-12-18	2017-07-18	Chevron Phillips Chemical Company Lp	Method for making polyalphaolefins using aluminum halide catalyzed oligomerization of olefins
US12054443B2 (en)	2022-08-11	2024-08-06	Chevron Phillips Chemical Company Lp	Methods for making linear internal olefins from mixtures of linear and branched olefins

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3876720A (en) *	1972-07-24	1975-04-08	Gulf Research Development Co	Internal olefin
US4229610A (en) *	1978-11-03	1980-10-21	Phillips Petroleum Company	Olefin double bond isomerization
CA1215963A (fr) *	1982-11-12	1986-12-30	Tenneco Oil Company	Isomerisation d'alcenes a l'aide d'un catalyseur a base de a1.sub.20.sub.3
US4587374A (en) *	1984-03-26	1986-05-06	Ethyl Corporation	Olefin isomerization process
EP0169250B1 (fr) †	1984-07-16	1989-04-19	Nippon Petrochemicals Company, Limited	Agent d'encollage pour papier
US4895997A (en) †	1988-08-31	1990-01-23	Shell Oil Company	Olefin isomerization process
US4902849A (en) *	1989-02-06	1990-02-20	Phillips Petroleum Company	Dehydrogenation process
US5189012A (en) *	1990-03-30	1993-02-23	M-I Drilling Fluids Company	Oil based synthetic hydrocarbon drilling fluid
DZ1577A1 (fr) *	1991-05-08	2002-02-17	Hoechst Ag	Emploi d'acetals.
FR2708597B1 (fr) *	1993-07-30	1995-09-29	Inst Francais Du Petrole	Procédé d'isomérisation d'oléfines sur des catalyseurs métalliques imprégnés de composés organiques soufrés avant chargement dans le réacteur.
DE4344064C1 (de) †	1993-12-23	1995-06-01	Hoechst Ag	Verfahren zur Herstellung von in alpha-Stellung durch einen Alkylrest substituierten Aldehyden
US5741759A (en) †	1994-02-02	1998-04-21	Chevron Chemical Company	Skeletally isomerized linear olefins
US5965783A (en) *	1994-02-02	1999-10-12	Chevron Chemical Company	Process for isomerizing olefins
DE69511941T2 (de) *	1994-02-02	2000-04-20	Chevron Chemical Co. Llc	Verfahren zur herstellung von skelettisomerisierten linearen olefinen
DE69611028T2 (de) *	1996-01-30	2001-07-19	Bp Amoco Corp., Chicago	Verfahren zur Isomerisierung von Olefinen
ATE208413T1 (de) *	1997-08-08	2001-11-15	Bp Amoco Corp	Basisöl für bohrspülmittel mit niedrigem stockpunkt

2000
- 2000-01-07 US US09/479,175 patent/US6407302B1/en not_active Expired - Lifetime
- 2000-10-23 CA CA002358924A patent/CA2358924C/fr not_active Expired - Lifetime
- 2000-10-23 RU RU2001121946/04A patent/RU2241695C2/ru active
- 2000-10-23 EP EP00992945A patent/EP1144349B2/fr not_active Expired - Lifetime
- 2000-10-23 CZ CZ20012796A patent/CZ303406B6/cs not_active IP Right Cessation
- 2000-10-23 AT AT00992945T patent/ATE331700T1/de not_active IP Right Cessation
- 2000-10-23 WO PCT/US2000/041437 patent/WO2001032590A2/fr not_active Ceased
- 2000-10-23 JP JP2001534746A patent/JP3771842B2/ja not_active Expired - Lifetime
- 2000-10-23 AU AU29168/01A patent/AU776570B2/en not_active Expired
- 2000-10-23 DE DE60029086T patent/DE60029086T3/de not_active Expired - Lifetime
- 2000-11-03 TW TW089123217A patent/TWI237013B/zh not_active IP Right Cessation
2001
- 2001-06-13 ZA ZA200104830A patent/ZA200104830B/en unknown
- 2001-07-02 NO NO20013296A patent/NO330309B1/no not_active IP Right Cessation

Also Published As

Publication number	Publication date
US6407302B1 (en)	2002-06-18
EP1144349A2 (fr)	2001-10-17
EP1144349B1 (fr)	2006-06-28
CA2358924C (fr)	2010-01-12
NO330309B1 (no)	2011-03-28
CZ20012796A3 (cs)	2001-11-14
DE60029086T3 (de)	2012-06-14
CZ303406B6 (cs)	2012-09-05
AU776570B2 (en)	2004-09-16
CA2358924A1 (fr)	2001-05-10
NO20013296D0 (no)	2001-07-02
NO20013296L (no)	2001-07-02
RU2241695C2 (ru)	2004-12-10
DE60029086D1 (de)	2006-08-10
EP1144349B2 (fr)	2011-10-05
ATE331700T1 (de)	2006-07-15
JP2003513057A (ja)	2003-04-08
JP3771842B2 (ja)	2006-04-26
DE60029086T2 (de)	2007-05-24
AU2916801A (en)	2001-05-14
WO2001032590A3 (fr)	2002-01-03
TWI237013B (en)	2005-08-01
WO2001032590A2 (fr)	2001-05-10

Publication	Publication Date	Title
AU776570B2 (en)	2004-09-16	Isomerization process
US5569642A (en)	1996-10-29	Synthetic paraffinic hydrocarbon drilling fluid
US5432152A (en)	1995-07-11	Invert drilling fluid
US6057272A (en)	2000-05-02	Drilling fluids comprising mostly linear olefins
US6054415A (en)	2000-04-25	Skeletally isomerized linear olefins
US5627143A (en)	1997-05-06	Wellbore fluid
CZ226296A3 (cs)	1998-06-17	Lineární olefiny isomerované ve skeletu jako složka vrtné kapaliny
IE63532B1 (en)	1995-05-03	Esters of carboxylic acids of medium chain-length as a component of the oil phase in invert drillingmuds
WO1997034963A1 (fr)	1997-09-25	Fluides de forage respectueux de l'environnement et performants
US20050236300A1 (en)	2005-10-27	Process for well fluids base oil via metathesis of alpha-olefins
AU1720099A (en)	1999-07-19	Invert emulsion drilling fluid containing mixtures of secondary esters obtained by conversion of olefins, and preparation thereof
US5776865A (en)	1998-07-07	Emulsifiable oil
US9580636B2 (en)	2017-02-28	Secondary esters, methods of making, and uses thereof
CA2554115C (fr)	2007-04-03	Fluide de puits de forage comportant une phase huileuse
EP1007601A1 (fr)	2000-06-14	Huile de base pour fluide de puits caracterisee par un point d'ecoulement basse temperature