MX336180B - Catalizador de hidrogenacion selectiva y metodos para elaborar y usar el mismo. - Google Patents

Catalizador de hidrogenacion selectiva y metodos para elaborar y usar el mismo.

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Publication number
MX336180B
MX336180B MX2014010761A MX2014010761A MX336180B MX 336180 B MX336180 B MX 336180B MX 2014010761 A MX2014010761 A MX 2014010761A MX 2014010761 A MX2014010761 A MX 2014010761A MX 336180 B MX336180 B MX 336180B
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MX
Mexico
Prior art keywords
palladium
catalyst
hydrogenation catalyst
supported
composition
Prior art date
Application number
MX2014010761A
Other languages
English (en)
Inventor
Tin-Tack Peter Cheung
Zongxuan Hong
Original Assignee
Chevron Phillips Chemical Co
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 Chevron Phillips Chemical Co filed Critical Chevron Phillips Chemical Co
Publication of MX336180B publication Critical patent/MX336180B/es

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    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/26Catalysts comprising hydrides, coordination complexes or organic compounds containing in addition, inorganic metal compounds not provided for in groups B01J31/02 - B01J31/24
    • B01J31/28Catalysts comprising hydrides, coordination complexes or organic compounds containing in addition, inorganic metal compounds not provided for in groups B01J31/02 - B01J31/24 of the platinum group metals, iron group metals or copper
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    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C5/00Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
    • C07C5/02Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by hydrogenation
    • C07C5/08Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by hydrogenation of carbon-to-carbon triple bonds
    • C07C5/09Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by hydrogenation of carbon-to-carbon triple bonds to carbon-to-carbon double bonds
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    • B01J23/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/38Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
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    • B01J23/66Silver or gold
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    • B01J27/13Platinum group metals
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    • B01J31/02Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/0234Nitrogen-, phosphorus-, arsenic- or antimony-containing compounds
    • B01J31/0271Nitrogen-, phosphorus-, arsenic- or antimony-containing compounds also containing elements or functional groups covered by B01J31/0201 - B01J31/0231
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    • B01J31/16Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/1616Coordination complexes, e.g. organometallic complexes, immobilised on an inorganic support, e.g. ship-in-a-bottle type catalysts
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    • B01J31/18Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms
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    • B01J31/16Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/18Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms
    • B01J31/1845Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms the ligands containing phosphorus
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    • B01J31/18Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms
    • B01J31/1845Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms the ligands containing phosphorus
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    • B01J31/18Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms
    • B01J31/1845Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms the ligands containing phosphorus
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    • B01J31/18Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms
    • B01J31/1845Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms the ligands containing phosphorus
    • B01J31/1875Phosphinites (R2P(OR), their isomeric phosphine oxides (R3P=O) and RO-substitution derivatives thereof)
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    • B01J31/16Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/24Phosphines, i.e. phosphorus bonded to only carbon atoms, or to both carbon and hydrogen atoms, including e.g. sp2-hybridised phosphorus compounds such as phosphabenzene, phosphole or anionic phospholide ligands
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    • B01J31/24Phosphines, i.e. phosphorus bonded to only carbon atoms, or to both carbon and hydrogen atoms, including e.g. sp2-hybridised phosphorus compounds such as phosphabenzene, phosphole or anionic phospholide ligands
    • B01J31/2404Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring
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    • B01J37/00Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
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    • B01J37/0201Impregnation
    • B01J37/0203Impregnation the impregnation liquid containing organic compounds
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    • C07C5/03Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by hydrogenation of non-aromatic carbon-to-carbon double bonds
    • C07C5/05Partial hydrogenation
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    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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    • C10G45/00Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds
    • C10G45/32Selective hydrogenation of the diolefin or acetylene compounds
    • C10G45/34Selective hydrogenation of the diolefin or acetylene compounds characterised by the catalyst used
    • C10G45/40Selective hydrogenation of the diolefin or acetylene compounds characterised by the catalyst used containing platinum group metals or compounds thereof
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    • B01J2231/641Hydrogenation of organic substrates, i.e. H2 or H-transfer hydrogenations, e.g. Fischer-Tropsch processes
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Abstract

La presente invención se relaciona con una composición que comprende un catalizador de hidrogenación soportado que comprende paladio y un compuesto de organofósforo, siendo el catalizador de hidrogenación soportado capaz de hidrogenar selectivamente hidrocarburos altamente insaturados a hidrocarburos insaturados. También se describe un método para elaborar un catalizador de hidrogenación selectiva que comprende poner en contacto un soporte con un compuesto que contiene paladio para formar una composición soportada de paladio, poner en contacto la composición soportada de paladio con un compuesto de organofósforo, para formar un precursor catalizador, y reducir el precursor catalizador para formar el catalizador. También se describe un método para hidrogenar selectivamente hidrocarburos altamente insaturados a una composición enriquecida en hidrocarburos insaturados, que comprende: poner en contacto un catalizador soportado que comprende paladio y un compuesto de organofósforo con una alimentación que comprende un hidrocarburo altamente insaturado, bajo condiciones apropiadas para hidrogenar por lo menos una porción de la alimentación de hidrocarburos altamente insaturados para formar la composición enriquecida en hidrocarburos insaturados.
MX2014010761A 2009-03-04 2010-02-23 Catalizador de hidrogenacion selectiva y metodos para elaborar y usar el mismo. MX336180B (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US15749109P 2009-03-04 2009-03-04
PCT/US2010/025038 WO2010101736A2 (en) 2009-03-04 2010-02-23 Selective hydrogenation catalyst and methods of making and using same

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MX336180B true MX336180B (es) 2016-01-11

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MX2011009006A MX2011009006A (es) 2009-03-04 2010-02-23 Catalizador de hidrogenacion selectiva y metodos para elaborar y usar el mismo.

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US (3) US8633127B2 (es)
EP (2) EP3144064B1 (es)
JP (1) JP5511853B2 (es)
KR (1) KR101697799B1 (es)
AR (2) AR075638A1 (es)
AU (1) AU2010221662B2 (es)
BR (1) BRPI1009225A2 (es)
CA (2) CA2753442C (es)
ES (1) ES2645100T3 (es)
IL (1) IL214927A0 (es)
MX (2) MX336180B (es)
PH (1) PH12015500779B1 (es)
SG (3) SG10201505698TA (es)
WO (1) WO2010101736A2 (es)

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MX336180B (es) 2009-03-04 2016-01-11 Chevron Phillips Chemical Co Catalizador de hidrogenacion selectiva y metodos para elaborar y usar el mismo.
US8969598B2 (en) 2011-06-24 2015-03-03 Eastman Chemical Company Production of cyclic acetals or ketals using liquid-phase acid catalysts
US9056313B2 (en) 2011-06-24 2015-06-16 Eastman Chemical Company Catalysts for the production of hydroxy ether hydrocarbons by vapor phase hydrogenolysis of cyclic acetals and ketals
US9000229B2 (en) 2011-06-24 2015-04-07 Eastman Chemical Company Production of hydroxy ether hydrocarbons by vapor phase hydrogenolysis of cyclic acetals and ketals
US9388105B2 (en) 2011-06-24 2016-07-12 Eastman Chemical Company Production of hydroxy ether hydrocarbons by liquid phase hydrogenolysis of cyclic acetals or cyclic ketals
US8829206B2 (en) 2011-06-24 2014-09-09 Eastman Chemical Company Production of cyclic acetals or ketals using solid acid catalysts
US8829207B2 (en) 2011-06-24 2014-09-09 Eastman Chemical Company Production of cyclic acetals by reactive distillation
US8785697B2 (en) 2011-06-24 2014-07-22 Eastman Chemical Company Nickel modified catalyst for the production of hydroxy ether hydrocarbons by vapor phase hydrogenolysis of cyclic acetals and ketals
US9108188B2 (en) 2012-03-07 2015-08-18 Chevoron Phillip Chemical Company, LP Selective hydrogenation catalyst and methods of making and using same
KR20160052588A (ko) * 2013-09-06 2016-05-12 셰브론 필립스 케미컬 컴퍼니 엘피 쌍봉 지지체를 포함하는 선택적 수소화 촉매 및 이의 제조 및 사용 방법
JP6075506B2 (ja) * 2014-04-22 2017-02-08 宇部興産株式会社 水素化触媒及びその製造方法、並びにそれを用いたシクロヘキサノン又はその誘導体の製造方法
US9511359B2 (en) * 2014-11-14 2016-12-06 Chevron Phillips Chemical Company Lp Selective hydrogenation catalyst and methods of making and using same
US9758446B2 (en) 2015-11-16 2017-09-12 Chevron Phillips Chemical Company Lp Selective hydrogenation using a flow index
US10232360B1 (en) * 2017-09-12 2019-03-19 Chevron Phillips Chemical Company, Lp Use of organic dopants to enhance acetylene hydrogenation catalysts
US10245583B1 (en) * 2017-09-12 2019-04-02 Chevron Phillips Chemical Company, Lp Use of charge-containing molecules linked with covalent bonds to enhance acetylene hydrogenation catalysts

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