SG11201402499WA - Mixed-phase operation of butenes metathesis process for maximizing propylene production - Google Patents

Mixed-phase operation of butenes metathesis process for maximizing propylene production

Info

Publication number
SG11201402499WA
SG11201402499WA SG11201402499WA SG11201402499WA SG11201402499WA SG 11201402499W A SG11201402499W A SG 11201402499WA SG 11201402499W A SG11201402499W A SG 11201402499WA SG 11201402499W A SG11201402499W A SG 11201402499WA SG 11201402499W A SG11201402499W A SG 11201402499WA
Authority
SG
Singapore
Prior art keywords
mixed
phase operation
propylene production
metathesis process
butenes
Prior art date
Application number
SG11201402499WA
Inventor
Scott A Stevenson
Travis Conant
Original Assignee
Saudi Basic Ind Corp
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.)
Filing date
Publication date
Application filed by Saudi Basic Ind Corp filed Critical Saudi Basic Ind Corp
Publication of SG11201402499WA publication Critical patent/SG11201402499WA/en

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C6/00—Preparation of hydrocarbons from hydrocarbons containing a different number of carbon atoms by redistribution reactions
    • C07C6/02—Metathesis reactions at an unsaturated carbon-to-carbon bond
    • C07C6/04—Metathesis reactions at an unsaturated carbon-to-carbon bond at a carbon-to-carbon double bond
    • 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
    • C07C5/32—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with formation of free hydrogen
    • C07C5/373—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with formation of free hydrogen with simultaneous isomerisation
    • C07C5/393—Preparation 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2521/00—Catalysts comprising the elements, oxides or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium or hafnium
    • C07C2521/02—Boron or aluminium; Oxides or hydroxides thereof
    • C07C2521/04—Alumina
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2521/00—Catalysts comprising the elements, oxides or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium or hafnium
    • C07C2521/10—Magnesium; Oxides or hydroxides thereof
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2523/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
    • C07C2523/16—Catalysts 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
    • C07C2523/20—Vanadium, niobium or tantalum
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2523/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
    • C07C2523/16—Catalysts 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
    • C07C2523/24—Chromium, molybdenum or tungsten
    • C07C2523/28—Molybdenum
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2523/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
    • C07C2523/16—Catalysts 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
    • C07C2523/24—Chromium, molybdenum or tungsten
    • C07C2523/30—Tungsten
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2523/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
    • C07C2523/16—Catalysts 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
    • C07C2523/32—Manganese, technetium or rhenium
    • C07C2523/36—Rhenium
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2523/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
    • C07C2523/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of noble metals
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2527/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
    • C07C2527/02—Sulfur, selenium or tellurium; Compounds thereof
    • C07C2527/04—Sulfides
    • C07C2527/047—Sulfides with chromium, molybdenum, tungsten or polonium
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2529/00—Catalysts comprising molecular sieves
    • C07C2529/04—Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites, pillared clays
    • C07C2529/06—Crystalline aluminosilicate zeolites; Isomorphous compounds thereof
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2531/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • C07C2531/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • C07C2531/20—Carbonyls

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)
SG11201402499WA 2011-12-08 2012-12-04 Mixed-phase operation of butenes metathesis process for maximizing propylene production SG11201402499WA (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
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

Publications (1)

Publication Number Publication Date
SG11201402499WA true SG11201402499WA (en) 2014-09-26

Family

ID=47352044

Family Applications (1)

Application Number Title Priority Date Filing Date
SG11201402499WA SG11201402499WA (en) 2011-12-08 2012-12-04 Mixed-phase operation of butenes metathesis process for maximizing propylene production

Country Status (7)

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

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111362771A (en) * 2013-11-20 2020-07-03 鲁姆斯科技公司 Olefin double bond isomerization catalyst with high toxicity resistance

Family Cites Families (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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 (en) * 1991-10-17 1993-04-27 Maruzen Petrochem Co Ltd Catalyst for disproportionating olefin and olefin disproportionation method using the same
FR2726487B1 (en) * 1994-11-04 1996-12-13 Inst Francais Du Petrole CATALYTIC COMPOSITIONS BASED ON RHENIUM AND ALUMINUM COMPOUNDS, THEIR PREPARATION AND THEIR USE FOR OLEFIN METATHESIS
FR2733986B1 (en) * 1995-05-11 1997-06-13 Inst Francais Du Petrole PROCESS AND INSTALLATION FOR THE CONVERSION OF OLEFINIC C4 CUTS INTO POLYISOBUTENES AND PROPYLENE
DE19746040A1 (en) * 1997-10-17 1999-04-22 Basf Ag Propene production giving high yield and selectivity by disproportionation of but-1-ene, but-2-ene and isobutene using a metathesis catalyst based on a transistion metal
US6583329B1 (en) * 1998-03-04 2003-06-24 Catalytic Distillation Technologies Olefin metathesis in a distillation column reactor
AU4925799A (en) * 1998-09-04 2000-03-27 Sasol Technology (Proprietary) Limited Production of propylene
FR2789072B1 (en) * 1999-01-29 2001-04-13 Inst Francais Du Petrole PROCESS FOR THE METATHESIS OF OLEFINS IN THE PRESENCE OF A CATALYST STABILIZING AGENT
DE19932060A1 (en) * 1999-07-12 2001-01-18 Basf Ag Process for the production of C¶5¶ / C¶6¶ olefins
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
AR074890A1 (en) * 2008-08-12 2011-02-23 Lummus Technology Inc INTEGRATED PROPYLENE PRODUCTION
JP2011098923A (en) * 2009-11-06 2011-05-19 Nippon Zeon Co Ltd Method for producing propylene
JP5463860B2 (en) * 2009-11-06 2014-04-09 日本ゼオン株式会社 Propylene production method
BR112012023261B1 (en) * 2010-03-15 2018-09-18 Total Res & Technology Feluy propylene production by dehydration and simultaneous isomerization of the isobutanol backbone over acid catalysts followed by metathesis
US8722950B2 (en) * 2010-04-26 2014-05-13 Saudi Basic Industries Corporation Process for producing propylene and aromatics from butenes by metathesis and aromatization

Also Published As

Publication number Publication date
CN103958448B (en) 2015-11-25
KR20140107314A (en) 2014-09-04
EP2788305A1 (en) 2014-10-15
WO2013085860A1 (en) 2013-06-13
US20130150643A1 (en) 2013-06-13
JP5916882B2 (en) 2016-05-11
JP2015500284A (en) 2015-01-05
CN103958448A (en) 2014-07-30

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