IN246332B - - Google Patents

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Publication number
IN246332B
IN246332B IN4524DE2005A IN246332B IN 246332 B IN246332 B IN 246332B IN 4524DE2005 A IN4524DE2005 A IN 4524DE2005A IN 246332 B IN246332 B IN 246332B
Authority
IN
India
Application number
Other languages
English (en)
Inventor
Marek Matusz
Wayne Errol Evans
Original Assignee
Shell Int Research
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=33299733&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=IN246332(B) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Shell Int Research filed Critical Shell Int Research
Publication of IN2005DE04524A publication Critical patent/IN2005DE04524A/en
Publication of IN246332B publication Critical patent/IN246332B/en

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/09—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by hydrolysis
    • C07C29/10—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by hydrolysis of ethers, including cyclic ethers, e.g. oxiranes
    • C07C29/103—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by hydrolysis of ethers, including cyclic ethers, e.g. oxiranes of cyclic ethers
    • C07C29/106—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by hydrolysis of ethers, including cyclic ethers, e.g. oxiranes of cyclic ethers of oxiranes
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D301/00—Preparation of oxiranes
    • C07D301/02—Synthesis of the oxirane ring
    • C07D301/03—Synthesis of the oxirane ring by oxidation of unsaturated compounds, or of mixtures of unsaturated and saturated compounds
    • C07D301/04—Synthesis of the oxirane ring by oxidation of unsaturated compounds, or of mixtures of unsaturated and saturated compounds with air or molecular oxygen
    • C07D301/08—Synthesis of the oxirane ring by oxidation of unsaturated compounds, or of mixtures of unsaturated and saturated compounds with air or molecular oxygen in the gaseous phase
    • C07D301/10—Synthesis of the oxirane ring by oxidation of unsaturated compounds, or of mixtures of unsaturated and saturated compounds with air or molecular oxygen in the gaseous phase with catalysts containing silver or gold
    • Y—GENERAL 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
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00—Technologies relating to chemical industry
    • Y02P20/50—Improvements relating to the production of bulk chemicals
    • Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Epoxy Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Catalysts (AREA)
IN4524DE2005 2003-04-07 2004-04-05 IN246332B (enExample)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US46090103P 2003-04-07 2003-04-07

Publications (2)

Publication Number Publication Date
IN2005DE04524A IN2005DE04524A (enExample) 2009-10-02
IN246332B true IN246332B (enExample) 2011-03-04

Family

ID=33299733

Family Applications (1)

Application Number Title Priority Date Filing Date
IN4524DE2005 IN246332B (enExample) 2003-04-07 2004-04-05

Country Status (12)

Country Link
US (1) US7348444B2 (enExample)
EP (1) EP1620414B2 (enExample)
JP (1) JP5227513B2 (enExample)
KR (1) KR101107477B1 (enExample)
CN (1) CN100482652C (enExample)
CA (1) CA2525520C (enExample)
DE (1) DE602004029247D1 (enExample)
IN (1) IN246332B (enExample)
MX (1) MX261656B (enExample)
RU (1) RU2345073C2 (enExample)
TW (1) TWI374773B (enExample)
WO (1) WO2004092148A2 (enExample)

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AU2003243757A1 (en) 2002-06-28 2004-01-19 Shell Oil Company A method for improving the selectivity of a catalyst and a process for the epoxidation of an olefin
US8357812B2 (en) * 2005-12-22 2013-01-22 Shell Oil Company Process for preparing a rejuvenated epoxidation catalyst
CN101384572A (zh) * 2005-12-22 2009-03-11 国际壳牌研究有限公司 制备可由环氧烷衍生的化学品的方法和适用于这一方法的反应器
US7932408B2 (en) * 2006-09-29 2011-04-26 Scientific Design Company, Inc. Catalyst with bimodal pore size distribution and the use thereof
US7977274B2 (en) 2006-09-29 2011-07-12 Sd Lizenzverwertungsgesellschaft Mbh & Co. Kg Catalyst with bimodal pore size distribution and the use thereof
KR101505216B1 (ko) * 2007-05-09 2015-03-23 셀 인터나쵸나아레 레사아치 마아츠샤피 비이부이 산화올레핀, 1,2-디올, 1,2-디올 에테르, 1,2-카보네이트 또는 알칸올아민의 생산 방법
KR20100017689A (ko) * 2007-05-09 2010-02-16 셀 인터나쵸나아레 레사아치 마아츠샤피 비이부이 에폭시화 촉매, 이 촉매의 제조방법, 및 산화올레핀, 1,2-디올, 1,2-디올 에테르, 1,2-카보네이트 또는 알칸올아민의 생산 방법
CA2687234C (en) 2007-05-11 2016-04-19 Sd Lizenzverwertungsgesellschaft Mbh & Co. Kg Start-up of high selectivity catalysts in olefin oxide plants
US9144765B2 (en) 2007-05-18 2015-09-29 Shell Oil Company Reactor system, an absorbent and a process for reacting a feed
TW200904524A (en) * 2007-05-18 2009-02-01 Shell Int Research A reactor system and process for reacting a feed
AR066574A1 (es) * 2007-05-18 2009-08-26 Shell Int Research Un sistema reactor, un proceso de produccion de oxido de olefina 1,2-diol 1,2-diol eter , 1,2-carbonato o alcanolamina
CN101687159B (zh) * 2007-05-18 2013-04-03 国际壳牌研究有限公司 反应器系统、吸收剂和用于使原料反应的方法
US8290626B2 (en) * 2007-09-10 2012-10-16 SD Lizenzverwertungsgesellschadt mbH & Co KG Chemical process optimization method that considers chemical process plant safety
KR101629037B1 (ko) 2008-05-07 2016-06-09 셀 인터나쵸나아레 레사아치 마아츠샤피 비이부이 에폭시화 방법의 스타트업 방법, 산화에틸렌, 1,2-디올, 1,2-디올 에테르, 1,2-카보네이트 또는 알칸올아민의 생산방법
EP2297125B1 (en) 2008-05-07 2013-07-03 Shell Internationale Research Maatschappij B.V. A process for the production of an olefin oxide, a 1,2-diol, a 1,2-diol ether, a 1,2-carbonate, or an alkanolamine
BRPI0912718B1 (pt) * 2008-05-15 2017-12-26 Shell Internationale Research Maataschappij B.V Method for producing an alkylene carbonate and / or an alkylene glycol
CN102066352B (zh) 2008-05-15 2014-03-19 国际壳牌研究有限公司 制备亚烷基碳酸酯和亚烷基二醇的方法
US20110152546A1 (en) 2009-12-17 2011-06-23 Sumitomo Chemical Company, Limited Process for producing olefin oxide
CA2749938C (en) * 2009-12-28 2018-10-16 Dow Technology Investments Llc Method of controlling the production of silver chloride on a silver catalyst in the production of alkylene oxides
US8546592B2 (en) 2010-09-29 2013-10-01 Shell Oil Company Olefin epoxidation process
US8742147B2 (en) 2010-12-08 2014-06-03 Shell Oil Company Process for improving the selectivity of an EO catalyst
US8742146B2 (en) 2010-12-08 2014-06-03 Shell Oil Company Process for improving the selectivity of an EO catalyst
WO2012082389A1 (en) 2010-12-15 2012-06-21 Dow Technology Investments Llc Method of starting-up a process of producing an alkylene oxide using a high-efficiency catalyst
WO2012149098A1 (en) * 2011-04-29 2012-11-01 Shell Oil Company Process for improving the selectivity of an eo catalyst
WO2013062791A1 (en) * 2011-10-24 2013-05-02 Sumitomo Chemical Company, Limited Process for producing olefin oxide
CA2858551C (en) 2011-12-09 2021-10-26 Dow Technology Investments Llc Method of maintaining the value of an alkylene oxide production parameter in a process of making an alkylene oxide using a high efficiency catalyst
WO2018102377A1 (en) 2016-12-02 2018-06-07 Shell Oil Company Methods for conditioning an ethylene epoxidation catalyst and associated methods for the production of ethylene oxide

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Also Published As

Publication number Publication date
US20040236124A1 (en) 2004-11-25
MX261656B (es) 2008-10-24
JP5227513B2 (ja) 2013-07-03
TWI374773B (en) 2012-10-21
KR20060028672A (ko) 2006-03-31
WO2004092148A2 (en) 2004-10-28
CN1791586A (zh) 2006-06-21
WO2004092148A3 (en) 2005-03-24
EP1620414B1 (en) 2010-09-22
RU2005134228A (ru) 2006-06-10
RU2345073C2 (ru) 2009-01-27
DE602004029247D1 (de) 2010-11-04
JP2006522155A (ja) 2006-09-28
EP1620414A2 (en) 2006-02-01
CA2525520A1 (en) 2004-10-28
EP1620414B2 (en) 2013-08-14
US7348444B2 (en) 2008-03-25
CN100482652C (zh) 2009-04-29
MXPA05010735A (es) 2006-05-25
TW200427508A (en) 2004-12-16
IN2005DE04524A (enExample) 2009-10-02
KR101107477B1 (ko) 2012-01-19
CA2525520C (en) 2012-03-13

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