BRPI1005294A2 - processo para contar um oxido de alquileno - Google Patents

processo para contar um oxido de alquileno

Info

Publication number
BRPI1005294A2
BRPI1005294A2 BRPI1005294A BRPI1005294A BRPI1005294A2 BR PI1005294 A2 BRPI1005294 A2 BR PI1005294A2 BR PI1005294 A BRPI1005294 A BR PI1005294A BR PI1005294 A BRPI1005294 A BR PI1005294A BR PI1005294 A2 BRPI1005294 A2 BR PI1005294A2
Authority
BR
Brazil
Prior art keywords
counting
alkylene oxide
alkylene
oxide
Prior art date
Application number
BRPI1005294A
Other languages
English (en)
Inventor
Verral Daniel
W Flick Derrick
Macdonald Jason
Degroot Marty
Elowe Paul
Nickias Peter
Arrowood Tina
Original Assignee
Dow Global Technologies Inc
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 Dow Global Technologies Inc filed Critical Dow Global Technologies Inc
Publication of BRPI1005294A2 publication Critical patent/BRPI1005294A2/pt
Publication of BRPI1005294B1 publication Critical patent/BRPI1005294B1/pt

Links

Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/22—Organic complexes
    • B01J31/2204—Organic complexes the ligands containing oxygen or sulfur as complexing atoms
    • B01J31/2208—Oxygen, e.g. acetylacetonates
    • B01J31/2226—Anionic ligands, i.e. the overall ligand carries at least one formal negative charge
    • B01J31/2243—At least one oxygen and one nitrogen atom present as complexing atoms in an at least bidentate or bridging ligand
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/1616—Coordination complexes, e.g. organometallic complexes, immobilised on an inorganic support, e.g. ship-in-a-bottle type catalysts
    • B01J31/1625—Coordination complexes, e.g. organometallic complexes, immobilised on an inorganic support, e.g. ship-in-a-bottle type catalysts immobilised by covalent linkages, i.e. pendant complexes with optional linking groups
    • B01J31/1633—Coordination complexes, e.g. organometallic complexes, immobilised on an inorganic support, e.g. ship-in-a-bottle type catalysts immobilised by covalent linkages, i.e. pendant complexes with optional linking groups covalent linkages via silicon containing groups
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/22—Organic complexes
    • B01J31/2204—Organic complexes the ligands containing oxygen or sulfur as complexing atoms
    • B01J31/2208—Oxygen, e.g. acetylacetonates
    • B01J31/2226—Anionic ligands, i.e. the overall ligand carries at least one formal negative charge
    • B01J31/2252—Sulfonate ligands
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C41/00—Preparation of ethers; Preparation of compounds having groups, groups or groups
    • C07C41/01—Preparation of ethers
    • C07C41/02—Preparation of ethers from oxiranes
    • C07C41/03—Preparation of ethers from oxiranes by reaction of oxirane rings with hydroxy groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C41/00—Preparation of ethers; Preparation of compounds having groups, groups or groups
    • C07C41/01—Preparation of ethers
    • C07C41/34—Separation; Purification; Stabilisation; Use of additives
    • C07C41/44—Separation; Purification; Stabilisation; Use of additives by treatments giving rise to a chemical modification
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J21/00—Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
    • B01J21/06—Silicon, titanium, zirconium or hafnium; Oxides or hydroxides thereof
    • B01J21/08—Silica
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
    • B01J2231/30—Addition reactions at carbon centres, i.e. to either C-C or C-X multiple bonds
    • B01J2231/34—Other additions, e.g. Monsanto-type carbonylations, addition to 1,2-C=X or 1,2-C-X triplebonds, additions to 1,4-C=C-C=X or 1,4-C=-C-X triple bonds with X, e.g. O, S, NH/N
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
    • B01J2231/30—Addition reactions at carbon centres, i.e. to either C-C or C-X multiple bonds
    • B01J2231/34—Other additions, e.g. Monsanto-type carbonylations, addition to 1,2-C=X or 1,2-C-X triplebonds, additions to 1,4-C=C-C=X or 1,4-C=-C-X triple bonds with X, e.g. O, S, NH/N
    • B01J2231/349—1,2- or 1,4-additions in combination with further or prior reactions by the same catalyst, i.e. tandem or domino reactions, e.g. hydrogenation or further addition reactions
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/02—Compositional aspects of complexes used, e.g. polynuclearity
    • B01J2531/0213—Complexes without C-metal linkages
    • B01J2531/0216—Bi- or polynuclear complexes, i.e. comprising two or more metal coordination centres, without metal-metal bonds, e.g. Cp(Lx)Zr-imidazole-Zr(Lx)Cp
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/02—Compositional aspects of complexes used, e.g. polynuclearity
    • B01J2531/0238—Complexes comprising multidentate ligands, i.e. more than 2 ionic or coordinative bonds from the central metal to the ligand, the latter having at least two donor atoms, e.g. N, O, S, P
    • B01J2531/0241—Rigid ligands, e.g. extended sp2-carbon frameworks or geminal di- or trisubstitution
    • B01J2531/0252—Salen ligands or analogues, e.g. derived from ethylenediamine and salicylaldehyde
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/80—Complexes comprising metals of Group VIII as the central metal
    • B01J2531/84—Metals of the iron group
    • B01J2531/845—Cobalt
BRPI1005294-1A 2009-02-26 2010-02-25 “processo para contatar um óxido de alquileno" BRPI1005294B1 (pt)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US15578609P 2009-02-26 2009-02-26
US61/155,786 2009-02-26
PCT/US2010/025389 WO2010099303A1 (en) 2009-02-26 2010-02-25 Alkoxylation processes and catalysts therefor

Publications (2)

Publication Number Publication Date
BRPI1005294A2 true BRPI1005294A2 (pt) 2017-06-06
BRPI1005294B1 BRPI1005294B1 (pt) 2018-06-26

Family

ID=42123068

Family Applications (4)

Application Number Title Priority Date Filing Date
BRPI1005370A BRPI1005370A2 (pt) 2009-02-26 2010-02-25 processo para contatar um óxido de alquileno
BRPI1005318A BRPI1005318A2 (pt) 2009-02-26 2010-02-25 composição
BRPI1005294-1A BRPI1005294B1 (pt) 2009-02-26 2010-02-25 “processo para contatar um óxido de alquileno"
BRPI1005290A BRPI1005290A2 (pt) 2009-02-26 2010-02-25 composição

Family Applications Before (2)

Application Number Title Priority Date Filing Date
BRPI1005370A BRPI1005370A2 (pt) 2009-02-26 2010-02-25 processo para contatar um óxido de alquileno
BRPI1005318A BRPI1005318A2 (pt) 2009-02-26 2010-02-25 composição

Family Applications After (1)

Application Number Title Priority Date Filing Date
BRPI1005290A BRPI1005290A2 (pt) 2009-02-26 2010-02-25 composição

Country Status (6)

Country Link
US (4) US20110297877A1 (pt)
EP (4) EP2401075A1 (pt)
CN (4) CN102325595B (pt)
BR (4) BRPI1005370A2 (pt)
TW (4) TWI469987B (pt)
WO (4) WO2010099307A1 (pt)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2013106290A (ru) 2010-07-14 2014-08-20 ДАУ ГЛОБАЛ ТЕКНОЛОДЖИЗ, ЭлЭлСи Способ и комплекс оборудования для производства алкиленоксидов и гликолевых простых эфиров
CN102964223A (zh) * 2012-11-13 2013-03-13 宁波杭州湾新区珠峰企业管理服务有限公司 丙二醇单甲醚的制备方法
CN103554483B (zh) * 2013-11-07 2015-12-30 南昌航空大学 一种手性聚席夫碱配合物材料
MY179337A (en) * 2014-06-17 2020-11-04 Sasol Usa Corp Catalyst compositions, methods of preparation thereof, and processes for alkoxylating alcohols using such catalysts
WO2016035805A1 (ja) * 2014-09-03 2016-03-10 丸善石油化学株式会社 触媒、その製造方法、及び前記触媒を用いるポリアルキレンカーボネートの製造方法
CN106732780A (zh) * 2015-11-20 2017-05-31 长春工业大学 一种有机硅负载Salen(Mn)的杂化材料、制备及用其制苯基环氧乙烷的方法
CN109054011B (zh) * 2018-07-16 2021-01-08 中国科学院长春应用化学研究所 一种席夫碱钴化合物、其制备方法及聚碳酸酯的制备方法
CN109225339B (zh) * 2018-09-28 2021-05-25 合肥工业大学 一种高活性协同mof催化剂的分级组装方法及应用
WO2023017794A1 (ja) 2021-08-10 2023-02-16 株式会社日本触媒 ポリアルキレンオキシド含有化合物

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TW224108B (pt) 1992-05-06 1994-05-21 Ciba Geigy
US6262278B1 (en) 1995-03-14 2001-07-17 President And Fellows Of Harvard College Stereoselective ring opening reactions
DE19525067A1 (de) 1995-07-10 1997-01-16 Buna Sow Leuna Olefinverb Gmbh Verfahren zur gleichzeitigen Herstellung von isomerenreinem Propylenglycol-mono-methylether und Dipropylenglycol-mono-methylether
US6492565B2 (en) 1998-10-07 2002-12-10 Bayer Aktiengesellschaft Process for the preparation of polyether polyols
WO2001000552A1 (en) 1999-06-30 2001-01-04 Union Carbide Chemicals & Plastics Technology Corporation Selective alkanol alkoxylations process
US6376721B1 (en) 2001-01-19 2002-04-23 Rhodia, Inc. Process for alkoxylation in the presence of rare earth triflimides
US6998497B2 (en) 2001-03-12 2006-02-14 The Queen's University Of Belfast Metal bis-triflimide compounds and methods for synthesis of metal bis-triflimide compounds
ES2327718T3 (es) 2001-04-18 2009-11-03 Sumitomo Chemical Company, Limited Catalizador complejo; su procedimiento de produccion y procedimiento de produccion de un derivado alcoholico realizado con este catalizador complejo.
CA2457211A1 (en) 2001-08-22 2003-03-06 Rhodia Pharma Solutions Inc. Improved hydrolytic kinetic resolution of epoxides
DE10164348A1 (de) * 2001-12-28 2003-07-17 Basf Ag Verfahren zur Herstellung von 1-Methoypropanol-2
JP2005305280A (ja) 2004-04-20 2005-11-04 Sanyo Chem Ind Ltd アルコキシ化反応触媒
US8207365B2 (en) * 2005-03-14 2012-06-26 Georgia Tech Research Corporation Polymeric salen compounds and methods thereof
CN100372972C (zh) * 2005-11-03 2008-03-05 复旦大学 在固体表面生长金属有机配合物的方法
US7482495B2 (en) * 2005-12-22 2009-01-27 Lyondell Chemical Technology, L.P. Process for making alkylene glycol ether compositions useful for metal recovery
KR20080019391A (ko) 2006-08-28 2008-03-04 주식회사 알에스텍 신규 이핵체 키랄 살렌 촉매 및 이를 이용한 키랄 화합물의제조방법
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KR100910067B1 (ko) * 2007-07-25 2009-09-10 주식회사 알에스텍 신규 바이메탈 살렌 촉매 및 이를 이용한 키랄 화합물의제조방법
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Also Published As

Publication number Publication date
TWI548613B (zh) 2016-09-11
CN102316982A (zh) 2012-01-11
TW201038521A (en) 2010-11-01
BRPI1005290A2 (pt) 2016-03-22
US20120029246A1 (en) 2012-02-02
CN102325594A (zh) 2012-01-18
US20110297877A1 (en) 2011-12-08
TWI469987B (zh) 2015-01-21
EP2401074A1 (en) 2012-01-04
TWI475024B (zh) 2015-03-01
US8835348B2 (en) 2014-09-16
EP2401076A1 (en) 2012-01-04
WO2010099307A1 (en) 2010-09-02
WO2010099309A1 (en) 2010-09-02
BRPI1005370A2 (pt) 2016-02-10
CN102316981B (zh) 2015-07-01
BRPI1005318A2 (pt) 2016-02-10
TW201036984A (en) 2010-10-16
TW201038582A (en) 2010-11-01
WO2010099303A1 (en) 2010-09-02
CN102325595A (zh) 2012-01-18
TWI483928B (zh) 2015-05-11
US8975446B2 (en) 2015-03-10
EP2401077A1 (en) 2012-01-04
US8748336B2 (en) 2014-06-10
CN102316981A (zh) 2012-01-11
BRPI1005294B1 (pt) 2018-06-26
US20120035383A1 (en) 2012-02-09
EP2401075A1 (en) 2012-01-04
TW201035004A (en) 2010-10-01
CN102325595B (zh) 2015-01-07
CN102325594B (zh) 2015-11-25
WO2010099300A1 (en) 2010-09-02
US20110301323A1 (en) 2011-12-08

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Legal Events

Date Code Title Description
B07A Application suspended after technical examination (opinion) [chapter 7.1 patent gazette]
B06A Patent application procedure suspended [chapter 6.1 patent gazette]
B09A Decision: intention to grant [chapter 9.1 patent gazette]
B16A Patent or certificate of addition of invention granted [chapter 16.1 patent gazette]
B21F Lapse acc. art. 78, item iv - on non-payment of the annual fees in time

Free format text: REFERENTE A 11A ANUIDADE.

B24J Lapse because of non-payment of annual fees (definitively: art 78 iv lpi, resolution 113/2013 art. 12)

Free format text: EM VIRTUDE DA EXTINCAO PUBLICADA NA RPI 2619 DE 16-03-2021 E CONSIDERANDO AUSENCIA DE MANIFESTACAO DENTRO DOS PRAZOS LEGAIS, INFORMO QUE CABE SER MANTIDA A EXTINCAO DA PATENTE E SEUS CERTIFICADOS, CONFORME O DISPOSTO NO ARTIGO 12, DA RESOLUCAO 113/2013.