CA2392233C - Procedes permettant d'eviter la generation d'halogenures d'hydrogene dans un systeme de recuperation de produits d'oligomerisation - Google Patents

Procedes permettant d'eviter la generation d'halogenures d'hydrogene dans un systeme de recuperation de produits d'oligomerisation Download PDF

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Publication number
CA2392233C
CA2392233C CA002392233A CA2392233A CA2392233C CA 2392233 C CA2392233 C CA 2392233C CA 002392233 A CA002392233 A CA 002392233A CA 2392233 A CA2392233 A CA 2392233A CA 2392233 C CA2392233 C CA 2392233C
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CA
Canada
Prior art keywords
process according
amine
catalyst system
catalyst
stabilizing material
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Expired - Fee Related
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CA002392233A
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English (en)
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CA2392233A1 (fr
Inventor
Jeffrey W. Freeman
Bruce E. Kreischer
Warren M. Ewert
Ronald D. Knudsen
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Phillips Petroleum Co
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Phillips Petroleum Co
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Publication date
Application filed by Phillips Petroleum Co filed Critical Phillips Petroleum Co
Publication of CA2392233A1 publication Critical patent/CA2392233A1/fr
Application granted granted Critical
Publication of CA2392233C publication Critical patent/CA2392233C/fr
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2/00Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
    • C07C2/02Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons
    • C07C2/04Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons by oligomerisation of well-defined unsaturated hydrocarbons without ring formation
    • C07C2/06Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons by oligomerisation of well-defined unsaturated hydrocarbons without ring formation of alkenes, i.e. acyclic hydrocarbons having only one carbon-to-carbon double bond
    • C07C2/08Catalytic processes
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/582Recycling of unreacted starting or intermediate materials

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  • 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)

Abstract

La présente invention concerne un procédé d'oligomérisation. Un catalyseur, une oléfine inférieure et un milieu de traitement sont décrits. L'oléfine inférieure réagit en présence du catalyseur pour produire une vapeur de produit comprenant un produit oléfine supérieure et un reste de catalyseur dispersé dans le milieu de traitement. La vapeur de produit résultante est traitée avec un matériau d'extinction. Ce matériau d'extinction peut être une amine primaire aliphatique, une amine secondaire aliphatique, un alcool ou une combinaison de ces derniers. On a remarqué que les matériaux d'extinction amine génèrent peu ou aucun halogénure d'hydrogène lorsqu'ils sont utilisés pour épuiser des catalyseurs d'oligomérisation. Les matériaux d'extinction alcool peuvent générer des halogénures d'hydrogène en utilisation. Ce problème peut être atténué, il faut alors traiter la vapeur de produit avec une matière de stabilisation qui forme un sel halogénure d'hydrogène stable. Des exemples de matières de stabilisation peuvent comprendre les amines aliphatiques, les amines aromatiques et les sels métalliques d'amides, de butoxydes ou d'acides carboxyliques.
CA002392233A 1999-12-29 2000-12-27 Procedes permettant d'eviter la generation d'halogenures d'hydrogene dans un systeme de recuperation de produits d'oligomerisation Expired - Fee Related CA2392233C (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US47368899A 1999-12-29 1999-12-29
US09/473,688 1999-12-29
PCT/US2000/035366 WO2001047839A1 (fr) 1999-12-29 2000-12-27 Procedes permettant d'eviter la generation d'halogenures d'hydrogene dans un systeme de recuperation de produits d'oligomerisation

Publications (2)

Publication Number Publication Date
CA2392233A1 CA2392233A1 (fr) 2001-07-05
CA2392233C true CA2392233C (fr) 2006-10-24

Family

ID=23880592

Family Applications (1)

Application Number Title Priority Date Filing Date
CA002392233A Expired - Fee Related CA2392233C (fr) 1999-12-29 2000-12-27 Procedes permettant d'eviter la generation d'halogenures d'hydrogene dans un systeme de recuperation de produits d'oligomerisation

Country Status (9)

Country Link
EP (1) EP1242341A4 (fr)
CN (1) CN1399620A (fr)
AU (1) AU773364B2 (fr)
CA (1) CA2392233C (fr)
GC (1) GC0000217A (fr)
MX (1) MXPA02005399A (fr)
RU (1) RU2249585C2 (fr)
WO (1) WO2001047839A1 (fr)
ZA (1) ZA200203457B (fr)

Families Citing this family (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TW200502038A (en) * 2003-03-14 2005-01-16 Chevron Phillips Chemical Co Process to decrease or eliminate corrosion from the decomposition of halide containing olefin catalysts
US20050187418A1 (en) 2004-02-19 2005-08-25 Small Brooke L. Olefin oligomerization
US7384886B2 (en) 2004-02-20 2008-06-10 Chevron Phillips Chemical Company Lp Methods of preparation of an olefin oligomerization catalyst
US20050187098A1 (en) 2004-02-20 2005-08-25 Knudsen Ronald D. Methods of preparation of an olefin oligomerization catalyst
US20070043181A1 (en) 2005-08-19 2007-02-22 Knudsen Ronald D Methods of preparation of an olefin oligomerization catalyst
US9550841B2 (en) 2004-02-20 2017-01-24 Chevron Phillips Chemical Company Lp Methods of preparation of an olefin oligomerization catalyst
US7902415B2 (en) 2007-12-21 2011-03-08 Chevron Phillips Chemical Company Lp Processes for dimerizing or isomerizing olefins
CN105753622B (zh) * 2008-01-30 2019-01-29 林德股份公司 制备线性α-烯烃的方法
CN102186587B (zh) 2008-10-31 2014-09-03 切弗朗菲利浦化学公司 去活化和猝灭低聚催化剂的系统和方法
ES2439261T3 (es) 2009-07-24 2014-01-22 Linde Ag Procedimiento de preparación de alfa-olefinas lineales
RU2471762C1 (ru) 2011-06-22 2013-01-10 Открытое акционерное общество "СИБУР Холдинг" (ОАО "СИБУР Холдинг") Способ выделения продуктов олигомеризации олефинов и разложения остатков катализатора олигомеризации
US9586872B2 (en) 2011-12-30 2017-03-07 Chevron Phillips Chemical Company Lp Olefin oligomerization methods
KR102113798B1 (ko) 2014-12-23 2020-05-21 퍼블릭 조인트 스톡 컴퍼니 “시부르 홀딩” 올레핀 올리고머화 반응에서 폴리머 및 불활성화된 유기금속 촉매의 침전 방법
WO2017010998A1 (fr) 2015-07-14 2017-01-19 Chevron Phillips Chemical Company Lp Compositions d'oléfines
CN108025996A (zh) * 2015-09-16 2018-05-11 沙特基础工业全球技术有限公司 用于烯烃低聚催化剂的失活的方法
US9512248B1 (en) 2015-12-28 2016-12-06 Chevron Phillips Chemical Company Lp Mixed decyl mercaptans compositions and use thereof as chain transfer agents
US9512071B1 (en) 2015-12-28 2016-12-06 Chevron Phillips Chemical Company Lp Mixed decyl mercaptans compositions and methods of making same
US10011564B2 (en) 2015-12-28 2018-07-03 Chevron Phillips Chemical Company Lp Mixed decyl mercaptans compositions and methods of making same
US10040758B2 (en) 2015-12-28 2018-08-07 Chevron Phillips Chemical Company Lp Mixed decyl mercaptans compositions and methods of making same
US10294200B2 (en) 2015-12-28 2019-05-21 Chevron Phillips Chemical Company, Lp Mixed branched eicosyl polysulfide compositions and methods of making same
US9505011B1 (en) 2015-12-28 2016-11-29 Chevron Phillips Chemical Company Lp Mixed decyl mercaptans compositions and use thereof as mining chemical collectors
EP3554664A1 (fr) * 2016-12-19 2019-10-23 SABIC Global Technologies B.V. Procédé de séparation d'alpha-oléfines linéaires
FR3103486A1 (fr) * 2019-11-26 2021-05-28 IFP Energies Nouvelles Procede de neutralisation d’une composition catalytique contenu dans un effluent issu d’une etape d’oligomerisation
FR3103485B1 (fr) * 2019-11-26 2023-03-24 Ifp Energies Now Procédé de séparation d’un effluent issu d’une étape d’oligomérisation

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4486615A (en) * 1960-09-14 1984-12-04 Exxon Research & Engineering Co. Preparation of linear olefin products
FR2581381B1 (fr) * 1985-05-02 1987-07-10 Inst Francais Du Petrole Procede de production de butene-1 de purete amelioree a partir du produit brut de dimersion de l'ethylene
EP0241596B1 (fr) * 1986-04-17 1990-10-31 Idemitsu Petrochemical Co. Ltd. Procédé pour la préparation d'alpha-oléfines linéaires
SU1662996A1 (ru) * 1987-07-13 1991-07-15 Отделение Института химической физики АН СССР Способ получени бутена-1
FR2715154B1 (fr) * 1994-01-14 1996-04-05 Inst Francais Du Petrole Procédé de production d'oléfines alpha légères de pureté améliorée par oligomérisation, de l'éthylène.
CA2134503C (fr) * 1994-02-18 2001-04-10 Mark E. Lashier Procede pour l'obtention d'olefines
FR2759922B1 (fr) * 1997-02-25 1999-05-07 Inst Francais Du Petrole Composition catalytique amelioree pour la conversion de l'ethylene en olefines alpha legeres

Also Published As

Publication number Publication date
CA2392233A1 (fr) 2001-07-05
MXPA02005399A (es) 2002-12-05
RU2249585C2 (ru) 2005-04-10
EP1242341A1 (fr) 2002-09-25
AU2600601A (en) 2001-07-09
AU773364B2 (en) 2004-05-20
ZA200203457B (en) 2003-10-29
CN1399620A (zh) 2003-02-26
WO2001047839A1 (fr) 2001-07-05
EP1242341A4 (fr) 2004-11-03
GC0000217A (en) 2006-03-29
RU2002120493A (ru) 2004-01-10

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Effective date: 20171227

MKLA Lapsed

Effective date: 20171227