KR970704516A - Shape selective hydrocarbon conversion (Shape selective hydrocarbon conversion) - Google Patents

Shape selective hydrocarbon conversion (Shape selective hydrocarbon conversion) Download PDF

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Publication number
KR970704516A
KR970704516A KR1019970700315A KR19970700315A KR970704516A KR 970704516 A KR970704516 A KR 970704516A KR 1019970700315 A KR1019970700315 A KR 1019970700315A KR 19970700315 A KR19970700315 A KR 19970700315A KR 970704516 A KR970704516 A KR 970704516A
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South Korea
Prior art keywords
molecular sieve
rti
organosilicon compound
catalyst
crystalline molecular
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KR1019970700315A
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Korean (ko)
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KR100248667B1 (en
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데이톤 창 클라렌스
팅-와 추 신티아
프란시스 데그난 주니어 토마스
게하르드 로데왈드 주니어 폴
세이드 시하비 데이비드
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데니스 피. 산티니
모빌 오일 코퍼레이션
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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J29/00Catalysts comprising molecular sieves
    • B01J29/04Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites
    • B01J29/06Crystalline aluminosilicate zeolites; Isomorphous compounds thereof
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J29/00Catalysts comprising molecular sieves
    • B01J29/04Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites
    • B01J29/06Crystalline aluminosilicate zeolites; Isomorphous compounds thereof
    • B01J29/40Crystalline aluminosilicate zeolites; Isomorphous compounds thereof of the pentasil type, e.g. types ZSM-5, ZSM-8 or ZSM-11, as exemplified by patent documents US3702886, GB1334243 and US3709979, respectively
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/02Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/0272Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing elements other than those covered by B01J31/0201 - B01J31/0255
    • B01J31/0274Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing elements other than those covered by B01J31/0201 - B01J31/0255 containing silicon
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/02Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/12Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides
    • B01J31/123Organometallic polymers, e.g. comprising C-Si bonds in the main chain or in subunits grafted to the main chain
    • B01J31/124Silicones or siloxanes or comprising such units
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C6/00Preparation of hydrocarbons from hydrocarbons containing a different number of carbon atoms by redistribution reactions
    • C07C6/08Preparation of hydrocarbons from hydrocarbons containing a different number of carbon atoms by redistribution reactions by conversion at a saturated carbon-to-carbon bond
    • C07C6/12Preparation of hydrocarbons from hydrocarbons containing a different number of carbon atoms by redistribution reactions by conversion at a saturated carbon-to-carbon bond of exclusively hydrocarbons containing a six-membered aromatic ring
    • C07C6/123Preparation of hydrocarbons from hydrocarbons containing a different number of carbon atoms by redistribution reactions by conversion at a saturated carbon-to-carbon bond of exclusively hydrocarbons containing a six-membered aromatic ring of only one hydrocarbon
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2229/00Aspects of molecular sieve catalysts not covered by B01J29/00
    • B01J2229/10After treatment, characterised by the effect to be obtained
    • B01J2229/12After treatment, characterised by the effect to be obtained to alter the outside of the crystallites, e.g. selectivation
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2229/00Aspects of molecular sieve catalysts not covered by B01J29/00
    • B01J2229/30After treatment, characterised by the means used
    • B01J2229/32Reaction with silicon compounds, e.g. TEOS, siliconfluoride
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2229/00Aspects of molecular sieve catalysts not covered by B01J29/00
    • B01J2229/30After treatment, characterised by the means used
    • B01J2229/42Addition of matrix or binder particles
    • 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
    • Y02P20/52Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Catalysts (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Soft Magnetic Materials (AREA)
  • Diaphragms For Electromechanical Transducers (AREA)
  • Analysing Materials By The Use Of Radiation (AREA)

Abstract

본 발명은 반응 스트림을 전환 조건하에서 유기 실리콘 화합물과 응집화시킴으로서 예비 선택화된 촉매성 분자체와 접촉시키는 방법을 포함하는, 톨루엔의 불균등화 반응과 같은 형상 선택적 탄화수소 전환 방법에 관한 것이다.The present invention is directed to a method for the selective oxidation of hydrocarbons, such as a disproportionation reaction of toluene, comprising contacting the reaction stream with the preselected catalytic molecular sieve by agglomeration with an organosilicon compound under conversion conditions.

Description

형상 선택적인 탄화수소의 전환 방법(Shape selective hydrocarbon conversion)Shape selective hydrocarbon conversion (Shape selective hydrocarbon conversion)

본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음Since this is a trivial issue, I did not include the contents of the text.

Claims (8)

결정성 분자체 및 유기 실리콘 화합물을 함유한 혼합물을 응집시킨 후 그 응집체를 하소(calcining)시킴으로서 예비 선택화된 1 내지 12의 속박지수(Constraint Index)를 갖는 결정성 분자체(molecular sieve)를 함유한 촉매.Crystalline molecular sieve having a Constraint Index of 1 to 12 preselected by aggregating the mixture containing the crystalline molecular sieve and the organosilicon compound and then calcining the aggregate, One catalyst. 제1항에 있어서, 유기 실리콘 화합물이 실리콘, 실란, 알콕시실란, 실록산 및 폴리실록산 중에서 선택된 것인 촉매.The catalyst according to claim 1, wherein the organosilicon compound is selected from silicon, silane, alkoxysilane, siloxane and polysiloxane. 제1항 또는 제2항에 있어서, 추가로 수소화/탈수소화 금속을 함유한 촉매.3. The catalyst according to claim 1 or 2, further comprising a hydrogenation / dehydrogenation metal. 1 내지 12의 속박지수를 가진 결정성 분자체 물질과 유기 실리콘 화합물을 분자체/유기 실리콘 화합물 중량비가 1/10내지 100/1이 되도록 함유하는 혼합물을 제조하고, 이 혼합물을 응집시킴을 특징으로 하여 촉매성 분자체를 예비 선택화시키는 방법.Characterized in that a mixture is prepared which comprises a crystalline molecular sieve material with a binding index of 1 to 12 and an organosilicon compound so that the molecular sieve / organosilicon compound weight ratio is 1/10 to 100/1 and the mixture is agglomerated Lt; RTI ID = 0.0 > molecular sieves. ≪ / RTI > 제30항에 있어서, 예비 선택화된 촉매성 분자체를 톨루엔 및 파라-크실렌의 선택화제인 2차 실리콘 공급원을 함유하는 혼합물과 적어도 1시간 동안 톨루엔을 크실렌으로 전환시키는 반응 조건하에서 접촉시켜 두번 개질된 촉매를 수득하는 단계를 추가로 포함하는 방법.31. The method of claim 30, wherein the pre-selected catalytic molecular sieve is contacted with a mixture containing a second silicon source which is a selective agent of toluene and para-xylene for at least 1 hour under reaction conditions to convert toluene to xylene, Lt; RTI ID = 0.0 > (I) < / RTI > catalyst. 탄화수소를 결정성 분자체 및 유기 실리콘 화합물을 함유한 혼합물을 응집시키고, 생성된 응집체를 하소시킴으로서 예비 선택화된 1-12의 속박지수를 가지며 결정성 분자체를 함유한 촉매와 접촉시킴을 특징으로 하는 형상 선택적 탄화수소 전환 방법.Characterized in that the hydrocarbon is contacted with a catalyst containing crystalline molecular sieves and having a binding constant of 1-12 preliminarily selected by agglomerating the mixture containing the crystalline molecular sieve and the organosilicon compound and calcining the resulting agglomerates / RTI > hydrocarbons. 제5항에 있어서, 형상 선택적 탄화수소 전환 방법이 톨루엔을 파라-크실렌으로 선택적으로 불균등화시키는 것인 방법.6. The process of claim 5, wherein the shape-selective hydrocarbon conversion process selectively disproportionates the toluene to para-xylene. 제6항에 있어서, 불균등화 반응이 350℃내지 540℃의 온도, 100내지 34500KPa(대기압 내지 5000psig) 의 압력, 0.1 내지 20의 WHSV, 및 0.1 내지 20의 수소 대 탄화수소 몰비의 조건하에서 수행되는 방법.The process according to claim 6, wherein the disproportionation reaction is carried out under conditions of a temperature of from 350 DEG C to 540 DEG C, a pressure of from 100 to 34500 KPa (atmospheric pressure to 5000 psig), a WHSV of from 0.1 to 20, and a hydrogen to hydrocarbon molar ratio of from 0.1 to 20 . ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.※ Note: It is disclosed by the contents of the first application.
KR1019970700315A 1994-07-21 1994-07-21 Shape selective hydrocarbon conversion KR100248667B1 (en)

Applications Claiming Priority (1)

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PCT/US1994/008239 WO1996003360A1 (en) 1993-02-25 1994-07-21 Shape selective hydrocarbon conversion

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KR970704516A true KR970704516A (en) 1997-09-06
KR100248667B1 KR100248667B1 (en) 2000-03-15

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AU (1) AU692177B2 (en)
CA (1) CA2195306A1 (en)
WO (1) WO1996003360A1 (en)

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US20140100401A1 (en) * 2011-05-09 2014-04-10 Saudi Basic Industries Corporation Catalyst for the alkylation of aromatic hydrocarbons
WO2017213668A1 (en) 2016-06-10 2017-12-14 Exxonmobil Research And Engineering Company Organosilica polymer catalysts and methods of making the same

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US4465886A (en) * 1983-06-09 1984-08-14 Mobil Oil Corporation Silica-modified catalyst and use for selective production of para-dialkyl substituted benzenes
US4594332A (en) * 1983-10-20 1986-06-10 Basf Aktiengesellschaft Preparation of hard, fracture-resistant catalysts from zeolite powder
US4582815A (en) * 1984-07-06 1986-04-15 Mobil Oil Corporation Extrusion of silica-rich solids
US4950835A (en) * 1989-10-24 1990-08-21 Taiwan Styrene Monomer Corporation Novel silicon-modified catalyst Si/HZSM-5, it's preparation, and a process for synthesizing high purity p-dialkyl benzene from monoalkyl benzene by using said catalyst
US5321183A (en) * 1992-03-12 1994-06-14 Mobil Oil Corp. Process for the regioselective conversion of aromatics to para-disubstituted benzenes

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KR100248667B1 (en) 2000-03-15
JPH10503419A (en) 1998-03-31
AU7668794A (en) 1996-02-22
CA2195306A1 (en) 1996-02-08
WO1996003360A1 (en) 1996-02-08
EP0804393A1 (en) 1997-11-05
AU692177B2 (en) 1998-06-04
EP0804393A4 (en) 1998-05-20

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