CN103958448B - 用于使丙烯生产最大化的丁烯易位方法的混合相操作 - Google Patents

用于使丙烯生产最大化的丁烯易位方法的混合相操作 Download PDF

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CN103958448B
CN103958448B CN201280059882.8A CN201280059882A CN103958448B CN 103958448 B CN103958448 B CN 103958448B CN 201280059882 A CN201280059882 A CN 201280059882A CN 103958448 B CN103958448 B CN 103958448B
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olefin
metathesis
reaction
pressure
butene
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Chinese (zh)
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CN103958448A (zh
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特拉维斯·科南特
斯科特·A·史蒂文森
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Saudi Basic Industries Corp
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Saudi Basic Industries Corp
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C6/00Preparation of hydrocarbons from hydrocarbons containing a different number of carbon atoms by redistribution reactions
    • C07C6/02Metathesis reactions at an unsaturated carbon-to-carbon bond
    • C07C6/04Metathesis reactions at an unsaturated carbon-to-carbon bond at a carbon-to-carbon double bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C5/00Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
    • C07C5/32Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with formation of free hydrogen
    • C07C5/373Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with formation of free hydrogen with simultaneous isomerisation
    • C07C5/393Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with formation of free hydrogen with simultaneous isomerisation with cyclisation to an aromatic six-membered ring, e.g. dehydrogenation of n-hexane to benzene
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2521/00Catalysts comprising the elements, oxides or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium or hafnium
    • C07C2521/02Boron or aluminium; Oxides or hydroxides thereof
    • C07C2521/04Alumina
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2521/00Catalysts comprising the elements, oxides or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium or hafnium
    • C07C2521/10Magnesium; Oxides or hydroxides thereof
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2523/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
    • C07C2523/16Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
    • C07C2523/20Vanadium, niobium or tantalum
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2523/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
    • C07C2523/16Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
    • C07C2523/24Chromium, molybdenum or tungsten
    • C07C2523/28Molybdenum
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2523/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
    • C07C2523/16Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
    • C07C2523/24Chromium, molybdenum or tungsten
    • C07C2523/30Tungsten
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2523/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
    • C07C2523/16Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
    • C07C2523/32Manganese, technetium or rhenium
    • C07C2523/36Rhenium
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2523/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
    • C07C2523/38Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of noble metals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2527/00Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
    • C07C2527/02Sulfur, selenium or tellurium; Compounds thereof
    • C07C2527/04Sulfides
    • C07C2527/047Sulfides with chromium, molybdenum, tungsten or polonium
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2529/00Catalysts comprising molecular sieves
    • C07C2529/04Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites, pillared clays
    • C07C2529/06Crystalline aluminosilicate zeolites; Isomorphous compounds thereof
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2531/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • C07C2531/16Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • C07C2531/20Carbonyls

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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)
CN201280059882.8A 2011-12-08 2012-12-04 用于使丙烯生产最大化的丁烯易位方法的混合相操作 Expired - Fee Related CN103958448B (zh)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US13/315,058 2011-12-08
US13/315,058 US20130150643A1 (en) 2011-12-08 2011-12-08 Mixed-phase operation of butenes metathesis process for maximizing propylene production
PCT/US2012/067667 WO2013085860A1 (en) 2011-12-08 2012-12-04 Mixed-phase operation of butenes metathesis process for maximizing propylene production

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CN103958448A CN103958448A (zh) 2014-07-30
CN103958448B true CN103958448B (zh) 2015-11-25

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US (1) US20130150643A1 (enExample)
EP (1) EP2788305A1 (enExample)
JP (1) JP5916882B2 (enExample)
KR (1) KR20140107314A (enExample)
CN (1) CN103958448B (enExample)
SG (1) SG11201402499WA (enExample)
WO (1) WO2013085860A1 (enExample)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PL3071538T3 (pl) * 2013-11-20 2021-09-06 Lummus Technology Llc Katalizator izomeryzacji podwójnego wiązania olefiny o wysokiej odporności na zatrucie
US10633306B2 (en) * 2017-06-06 2020-04-28 Liquidpower Specialty Products Inc. Method of increasing alpha-olefin content
WO2025157807A1 (en) * 2024-01-24 2025-07-31 Sabic Global Technologies B.V. Systems and methods of producing hex-1-ene, ethene, and propene using low-temperature metathesis

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2011113836A1 (en) * 2010-03-15 2011-09-22 Total Petrochemicals Research Feluy Production of propylene via simultaneous dehydration and skeletal isomerisation of isobutanol on acid catalysts followed by metathesis

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US3676520A (en) * 1964-12-31 1972-07-11 Phillips Petroleum Co Conversion of olefins
US4151071A (en) * 1977-07-26 1979-04-24 Phillips Petroleum Company Dehydrocyclization process
US4709115A (en) * 1986-05-15 1987-11-24 The Dow Chemical Company Disproportionation of alkenes
US5026936A (en) * 1989-10-02 1991-06-25 Arco Chemical Technology, Inc. Enhanced production of propylene from higher hydrocarbons
JPH05103995A (ja) * 1991-10-17 1993-04-27 Maruzen Petrochem Co Ltd オレフインの不均化触媒およびその触媒を用いたオレフインの不均化方法
FR2726487B1 (fr) * 1994-11-04 1996-12-13 Inst Francais Du Petrole Compositions catalytiques a base de composes du rhenium et de l'aluminium leur preparation et leur utilisation pour la metathese des olefines
FR2733986B1 (fr) * 1995-05-11 1997-06-13 Inst Francais Du Petrole Procede et installation pour la conversion de coupes c4 olefiniques en polyisobutenes et en propylene
DE19746040A1 (de) * 1997-10-17 1999-04-22 Basf Ag Verfahren zur Herstellung von Propen
US6583329B1 (en) * 1998-03-04 2003-06-24 Catalytic Distillation Technologies Olefin metathesis in a distillation column reactor
US6586649B1 (en) * 1998-09-04 2003-07-01 Sasol Technology (Proprietary) Limited Production of propylene
FR2789072B1 (fr) * 1999-01-29 2001-04-13 Inst Francais Du Petrole Procede de metathese des olefines en presence d'un agent stabilisant du catalyseur
DE19932060A1 (de) * 1999-07-12 2001-01-18 Basf Ag Verfahren zur Herstellung von C¶5¶-/C¶6¶-Olefinen
US6743958B2 (en) * 1999-12-24 2004-06-01 Institut Francais Du Petrole Process for selective production of propylene from hydrocarbon fractions with four carbon atoms
US6777582B2 (en) 2002-03-07 2004-08-17 Abb Lummus Global Inc. Process for producing propylene and hexene from C4 olefin streams
EP1932820A1 (en) * 2006-12-14 2008-06-18 Bp Oil International Limited Process for manufacturing neohexene
US20080146856A1 (en) * 2006-12-19 2008-06-19 Leyshon David W Propylene production
CA2733890C (en) * 2008-08-12 2013-10-01 Lummus Technology Inc. Integrated propylene production
JP2011098923A (ja) * 2009-11-06 2011-05-19 Nippon Zeon Co Ltd プロピレンの製造方法
JP5463860B2 (ja) * 2009-11-06 2014-04-09 日本ゼオン株式会社 プロピレンの製造方法
US8722950B2 (en) * 2010-04-26 2014-05-13 Saudi Basic Industries Corporation Process for producing propylene and aromatics from butenes by metathesis and aromatization

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2011113836A1 (en) * 2010-03-15 2011-09-22 Total Petrochemicals Research Feluy Production of propylene via simultaneous dehydration and skeletal isomerisation of isobutanol on acid catalysts followed by metathesis

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Publication number Publication date
US20130150643A1 (en) 2013-06-13
JP5916882B2 (ja) 2016-05-11
CN103958448A (zh) 2014-07-30
EP2788305A1 (en) 2014-10-15
KR20140107314A (ko) 2014-09-04
JP2015500284A (ja) 2015-01-05
WO2013085860A1 (en) 2013-06-13
SG11201402499WA (en) 2014-09-26

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