AR057572A1 - Composiciones de catalizador y proceso para oxicloracion - Google Patents
Composiciones de catalizador y proceso para oxicloracionInfo
- Publication number
- AR057572A1 AR057572A1 ARP060104971A ARP060104971A AR057572A1 AR 057572 A1 AR057572 A1 AR 057572A1 AR P060104971 A ARP060104971 A AR P060104971A AR P060104971 A ARP060104971 A AR P060104971A AR 057572 A1 AR057572 A1 AR 057572A1
- Authority
- AR
- Argentina
- Prior art keywords
- oxychlorination
- catalyst
- diluent
- effective amount
- catalytically effective
- Prior art date
Links
- 239000003054 catalyst Substances 0.000 title abstract 10
- 239000000203 mixture Substances 0.000 title abstract 5
- 239000003085 diluting agent Substances 0.000 abstract 4
- 239000004215 Carbon black (E152) Substances 0.000 abstract 2
- 239000003153 chemical reaction reagent Substances 0.000 abstract 2
- 229930195733 hydrocarbon Natural products 0.000 abstract 2
- 150000002430 hydrocarbons Chemical class 0.000 abstract 2
- 239000003701 inert diluent Substances 0.000 abstract 2
- 239000000463 material Substances 0.000 abstract 2
- 239000002245 particle Substances 0.000 abstract 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 abstract 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 abstract 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/093—Preparation of halogenated hydrocarbons by replacement by halogens
- C07C17/15—Preparation of halogenated hydrocarbons by replacement by halogens with oxygen as auxiliary reagent, e.g. oxychlorination
- C07C17/152—Preparation of halogenated hydrocarbons by replacement by halogens with oxygen as auxiliary reagent, e.g. oxychlorination of hydrocarbons
-
- 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
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
- B01J23/72—Copper
-
- 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
- B01J21/12—Silica and alumina
-
- 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
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
- B01J23/76—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
- B01J23/83—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36 with rare earths or actinides
-
- 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
- B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- B01J27/06—Halogens; Compounds thereof
- B01J27/08—Halides
- B01J27/122—Halides of copper
-
- 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
- B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
- B01J27/06—Halogens; Compounds thereof
- B01J27/138—Halogens; Compounds thereof with alkaline earth metals, magnesium, beryllium, zinc, cadmium or mercury
-
- 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
- B01J35/00—Catalysts, in general, characterised by their form or physical properties
- B01J35/19—Catalysts containing parts with different compositions
-
- 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
- B01J35/00—Catalysts, in general, characterised by their form or physical properties
- B01J35/30—Catalysts, in general, characterised by their form or physical properties characterised by their physical properties
-
- 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
- B01J35/00—Catalysts, in general, characterised by their form or physical properties
- B01J35/30—Catalysts, in general, characterised by their form or physical properties characterised by their physical properties
- B01J35/31—Density
-
- 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
- B01J35/00—Catalysts, in general, characterised by their form or physical properties
- B01J35/60—Catalysts, in general, characterised by their form or physical properties characterised by their surface properties or porosity
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/093—Preparation of halogenated hydrocarbons by replacement by halogens
- C07C17/15—Preparation of halogenated hydrocarbons by replacement by halogens with oxygen as auxiliary reagent, e.g. oxychlorination
- C07C17/152—Preparation of halogenated hydrocarbons by replacement by halogens with oxygen as auxiliary reagent, e.g. oxychlorination of hydrocarbons
- C07C17/154—Preparation of halogenated hydrocarbons by replacement by halogens with oxygen as auxiliary reagent, e.g. oxychlorination of hydrocarbons of saturated hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/093—Preparation of halogenated hydrocarbons by replacement by halogens
- C07C17/15—Preparation of halogenated hydrocarbons by replacement by halogens with oxygen as auxiliary reagent, e.g. oxychlorination
- C07C17/152—Preparation of halogenated hydrocarbons by replacement by halogens with oxygen as auxiliary reagent, e.g. oxychlorination of hydrocarbons
- C07C17/156—Preparation of halogenated hydrocarbons by replacement by halogens with oxygen as auxiliary reagent, e.g. oxychlorination of hydrocarbons of unsaturated hydrocarbons
-
- 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
- B01J35/00—Catalysts, in general, characterised by their form or physical properties
- B01J35/40—Catalysts, in general, characterised by their form or physical properties characterised by dimensions, e.g. grain size
-
- 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
- B01J35/00—Catalysts, in general, characterised by their form or physical properties
- B01J35/60—Catalysts, in general, characterised by their form or physical properties characterised by their surface properties or porosity
- B01J35/61—Surface area
- B01J35/613—10-100 m2/g
-
- 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
- B01J35/00—Catalysts, in general, characterised by their form or physical properties
- B01J35/60—Catalysts, in general, characterised by their form or physical properties characterised by their surface properties or porosity
- B01J35/61—Surface area
- B01J35/615—100-500 m2/g
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Catalysts (AREA)
Abstract
Reivindicacion 1: Una composicion de catalizador para oxicloracion caracterizada porque comprende una cantidad catalíticamente eficaz de un catalizador para oxicloracion y un diluyente que comprende partículas de un silicato de alumina. Reivindicacion 3: Una composicion de catalizador para oxicloracion caracterizada porque comprende: a) una cantidad catalíticamente eficaz de un catalizador para oxicloracion presentando un área superficial mayor que 25 m2/g, en donde el catalizador para oxicloracion comprende un material de soporte teniendo distribuido en él una composicion de sal activa; y b) un diluyente presentando un área superficial entre cerca de 0,1 m2/g a cerca de 25 m2/g, en donde el material de soporte y el diluyente son diferentes químicamente y el tamano promedio de partículas del catalizador y el diluyente se encuentra entre cerca de 5 a cerca de 300 micrones. Reivindicacion 31: Un proceso de oxicloracion de un hidrocarburo caracterizado porque comprende la etapa de hacer entrar en contacto reactivos incluyendo el hidrocarburo, una fuente de cloruro y una fuente de oxígeno con una composicion de catalizador para oxicloracion comprendiendo una cantidad catalíticamente eficaz de un catalizador para oxicloracion y un diluyente inerte bajo condiciones de proceso para preparar un hidrocarburo clorado, en donde el proceso se desarrolla a una Topt(2), la temperatura de operacion optima del proceso, la cual es al menos cerca de 1sC superior que Topt(1), la temperatura de operacion optima de un proceso usando el mismo reactor, reactivos, cantidad de carga en el reactor, índices de produccion y catalizador para oxicloracion aunque son el diluyente inerte.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US73652405P | 2005-11-14 | 2005-11-14 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR057572A1 true AR057572A1 (es) | 2007-12-05 |
Family
ID=37769396
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP060104971A AR057572A1 (es) | 2005-11-14 | 2006-11-14 | Composiciones de catalizador y proceso para oxicloracion |
Country Status (18)
Country | Link |
---|---|
US (2) | US7585806B2 (es) |
EP (1) | EP1948358B1 (es) |
JP (1) | JP2009515684A (es) |
KR (2) | KR100995947B1 (es) |
CN (1) | CN101351266B (es) |
AR (1) | AR057572A1 (es) |
AT (1) | ATE540755T1 (es) |
BR (1) | BRPI0618386B1 (es) |
EG (1) | EG25821A (es) |
ES (1) | ES2378084T3 (es) |
MY (1) | MY155020A (es) |
NO (1) | NO338431B1 (es) |
PL (1) | PL1948358T3 (es) |
RU (1) | RU2387479C2 (es) |
TW (1) | TWI341218B (es) |
UA (1) | UA95620C2 (es) |
WO (1) | WO2007059424A1 (es) |
ZA (1) | ZA200804040B (es) |
Families Citing this family (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5084135B2 (ja) * | 2005-11-24 | 2012-11-28 | 日揮触媒化成株式会社 | オキシクロリネーション用触媒およびその製造方法 |
US7595276B2 (en) * | 2007-07-30 | 2009-09-29 | Jgc Catalysts And Chemicals Ltd. | Catalytic composition for oxychlorination |
US8030530B2 (en) * | 2008-06-17 | 2011-10-04 | Stauffer John E | Swing reactor and process for oxychlorination |
US20090312592A1 (en) * | 2008-06-17 | 2009-12-17 | Stauffer John E | Swing Reactor and Process for Oxychlorination |
CN102049314B (zh) * | 2009-10-30 | 2013-12-04 | 北京三聚环保新材料股份有限公司 | 一种微球形乙烯氧氯化催化剂制备方法 |
CN102049260B (zh) * | 2009-10-30 | 2013-12-11 | 北京三聚环保新材料股份有限公司 | 一种微球形乙烯氧氯化催化剂及其制备方法 |
RU2664799C2 (ru) * | 2012-11-05 | 2018-08-22 | Басф Корпорейшн | Катализатор для оксихлорирования этилена до 1,2-дихлорэтана |
US9248434B2 (en) * | 2012-11-06 | 2016-02-02 | Basf Corporation | Catalyst for the oxychlorination of ethylene to 1, 2-dichloroethane |
JP6509807B2 (ja) | 2013-03-15 | 2019-05-08 | オキシ ヴィニールズ,エルピー | ジクロロエタンへのエチレンのオキシ塩素化のための触媒及びプロセス |
JP2015147163A (ja) * | 2014-02-05 | 2015-08-20 | 東ソー株式会社 | 1,2−ジクロロエタン製造用触媒システムおよびそれを用いた1,2−ジクロロエタンの製造方法 |
MY195083A (en) * | 2014-06-23 | 2023-01-09 | Oxy Vinyls Lp | Catalyst and Process for Oxychlorination of Ethylene to Dichloroethane |
RU2639151C1 (ru) * | 2016-10-17 | 2017-12-20 | Общество с ограниченной ответственностью "Компания "Новые технологии"" | Способ получения микросферического катализатора окислительного хлорирования этилена |
JP7064216B2 (ja) * | 2019-02-27 | 2022-05-10 | 国立大学法人 東京大学 | アルコキシビニリデン化合物の製造方法、ピラゾール化合物の製造方法 |
CN114433099B (zh) * | 2020-10-16 | 2024-02-20 | 中国石油化工股份有限公司 | 一种适用于乙烯氧氯化反应的催化剂及其制备方法和应用 |
WO2023141486A1 (en) | 2022-01-19 | 2023-07-27 | Oxy Vinyls, Lp | Oxychlorination process |
Family Cites Families (83)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1618693B1 (de) | 1966-06-08 | 1971-11-11 | Marathon Oil Co | Verfahren zur Herstellung von Vinylchlorid und/oder Dichloräthan |
US3992463A (en) | 1967-05-19 | 1976-11-16 | Produits Chimiques Pechiney-Saint Gobain | Oxychlorination of ethylene with a fixed bed catalyst |
FR2242143B1 (es) * | 1973-09-04 | 1978-03-24 | Rhone Progil | |
JPS5411358B2 (es) | 1974-02-01 | 1979-05-14 | ||
US4172052A (en) | 1977-11-25 | 1979-10-23 | Ppg Industries, Inc. | Catalyst for production of ethylene dichloride |
US4226798A (en) | 1978-10-06 | 1980-10-07 | The B. F. Goodrich Company | Method of selecting operation of a fluid-bed reactor and apparatus for doing so |
US4246039A (en) | 1979-01-08 | 1981-01-20 | Engelhard Minerals & Chemicals Corporation | Kaolin clay processing |
US4228798A (en) * | 1979-05-01 | 1980-10-21 | Deaton David W | Suction receptacle with hygroscopic filter |
DE2922375A1 (de) | 1979-06-01 | 1980-12-11 | Hoechst Ag | Verfahren zur herstellung von 1,2-dichlorethan |
DE2925625C2 (de) | 1979-06-26 | 1981-10-01 | Chemische Werke Hüls AG, 4370 Marl | Verfahren zur Steigerung der Aktivität und zur Verlängerung der Standzeit bei hoher Selektivität von Silber-Träger-Katalysatoren für den Einsatz zur Ethylenoxid-Synthese |
US4446249A (en) | 1979-11-05 | 1984-05-01 | The B. F. Goodrich Company | Copper catalyst compositions for fluid-bed oxyhydrochlorination of ethylene |
US4339620A (en) | 1979-11-05 | 1982-07-13 | The B. F. Goodrich Company | Copper-catalyzed fluid-bed ethylene oxhydrochlorination process |
JPS5689058A (en) | 1979-12-21 | 1981-07-20 | Toyo Soda Mfg Co Ltd | Method for analyzing hydrocarbon compound |
JPS572224A (en) * | 1980-06-06 | 1982-01-07 | Tokuyama Soda Co Ltd | Oxyhalogenation |
US4427450A (en) | 1980-08-04 | 1984-01-24 | Engelhard Corporation | Chalking-resistant, calcined kaolin clay pigment and method of making |
DE3043442A1 (de) | 1980-11-18 | 1982-06-24 | Wacker-Chemie GmbH, 8000 München | Verfahren zur reinigung von durch thermische 1,2-dichlorethanspaltung gewonnenem chlorwasserstoff |
JPS6055177B2 (ja) | 1981-02-18 | 1985-12-04 | 鐘淵化学工業株式会社 | 触媒希釈剤 |
US4525518A (en) | 1981-12-02 | 1985-06-25 | Engelhard Corporation | Chalking-resistant, calcined kaolin clay pigment and method of making |
US4493902A (en) | 1983-02-25 | 1985-01-15 | Engelhard Corporation | Fluid catalytic cracking catalyst comprising microspheres containing more than about 40 percent by weight Y-faujasite and methods for making |
JPS6049004A (ja) | 1983-08-30 | 1985-03-18 | Toa Nenryo Kogyo Kk | α―オレフイン重合用触媒成分 |
US4578118A (en) | 1985-02-13 | 1986-03-25 | Engelhard Corporation | Kaolin clay-based pigment |
DE3608043A1 (de) | 1986-03-11 | 1987-09-17 | Wacker Chemie Gmbh | Verbessertes verfahren zur herstellung von 1,2-dichlorethan durch gasphasenchlorierung von ethylenhaltigen gasen |
US4678517A (en) | 1986-07-25 | 1987-07-07 | E.C.C. America Inc. | Method for calcining kaolin |
US4740642A (en) | 1986-08-21 | 1988-04-26 | The Bf Goodrich Company | Catalyst and process for the fluid-bed oxychlorination of ethylene to EDC |
US4849393A (en) * | 1986-08-21 | 1989-07-18 | The B.F. Goodrich Company | Catalyst and process for the fluid-bed oxychlorination of ethylene to EDC |
JPS6398483A (ja) | 1986-10-16 | 1988-04-28 | Kureha Chem Ind Co Ltd | 感圧記録用顕色剤シ−トの製造方法 |
JPH07117746B2 (ja) | 1987-04-16 | 1995-12-18 | 富士写真フイルム株式会社 | 感光性平版印刷版の製造方法 |
US5023220A (en) | 1988-11-16 | 1991-06-11 | Engelhard Corporation | Ultra high zeolite content FCC catalysts and method for making same from microspheres composed of a mixture of calcined kaolin clays |
FR2641779B1 (fr) * | 1988-12-26 | 1991-04-19 | Atochem | Procede et catalyseur d'oxychloration, leur application a la production du 1-2 dichloroethane |
US5006574A (en) | 1989-02-10 | 1991-04-09 | Engelhard Corporation | Cationcally dispersed slurries of calcined kaolin clay |
CA2013619C (en) | 1989-05-04 | 1996-06-18 | Steven A. Brown | Cationic processing of kaolin ores |
US5112782A (en) | 1989-05-04 | 1992-05-12 | Engelhard Corporation | Cationically processed calcined kaolin clay |
US5202511A (en) * | 1989-08-16 | 1993-04-13 | The Dow Chemical Company | Catalyst diluent for oxychlorination process |
US5039821A (en) | 1989-08-23 | 1991-08-13 | Appleton Papers Inc. | Process for producing di[bis-(indolyl)ethylenyl]tetrahalophthalides |
US5733572A (en) | 1989-12-22 | 1998-03-31 | Imarx Pharmaceutical Corp. | Gas and gaseous precursor filled microspheres as topical and subcutaneous delivery vehicles |
US5011534A (en) | 1990-02-14 | 1991-04-30 | Engelhard Corporation | Calcined kaolin clay filler pigment for enhancing opacity and printing properties of newsprint and mechanical papers |
US5074475A (en) | 1990-03-26 | 1991-12-24 | E.C.C. America Inc. | Method for improving bulk density and flowability of calcined kaolin clay products |
US5028268A (en) | 1990-03-26 | 1991-07-02 | E.C.C. America Inc. | Method for improving the rheology of calcined kaolin clay products |
US5129953A (en) | 1990-03-26 | 1992-07-14 | E.C.C. America, Inc. | Method for improving bulk density and flowability of calcined kaolin clay products |
FR2663629B1 (fr) * | 1990-06-25 | 1992-12-18 | Atochem | Procede et catalyseur d'oxychloration, leur application a la production du 1-2 dichloroethane. |
US5243111A (en) | 1990-06-25 | 1993-09-07 | Atochem | Catalytic oxychlorination of hydrocarbons to produce chlorocarbons |
US5261956A (en) | 1990-07-03 | 1993-11-16 | Ecc International Inc. | Method for improving the rheology of calcined kaolin clay products |
US5292703A (en) * | 1992-07-28 | 1994-03-08 | The Geon Company | Catalyst and process for oxychlorination of ethylene to EDC |
BR9303410A (pt) | 1992-08-26 | 1994-03-22 | Engelhard Corp | Pigmentos de caulim calcinados,e processo para produzir os mesmos |
FI96848C (fi) * | 1993-02-22 | 1996-09-10 | Pentti Valoranta | Hienojakoista alkalisilikaattia sisältävä jauhemainen tuote ja sen valmistusmenetelmä |
JPH07138015A (ja) * | 1993-06-15 | 1995-05-30 | Catalysts & Chem Ind Co Ltd | シリカ微小球状粒子およびその製造方法 |
US5478867A (en) | 1993-07-07 | 1995-12-26 | The Dow Chemical Company | Microporous isocyanate-based polymer compositions and method of preparation |
US5468819A (en) | 1993-11-16 | 1995-11-21 | The B.F. Goodrich Company | Process for making polymers containing a norbornene repeating unit by addition polymerization using an organo (nickel or palladium) complex |
JPH07176103A (ja) | 1993-12-20 | 1995-07-14 | Canon Inc | 光磁気記録再生システムならびにこれに用いる磁気ヘッド及び光磁気記録媒体 |
GB2294262B (en) | 1994-10-20 | 1998-07-08 | Evc Tech Ag | Single stage fixed bed oxychlorination of ethylene |
US6030698A (en) * | 1994-12-19 | 2000-02-29 | Lockheed Martin Energy Research Corporation | Activated carbon fiber composite material and method of making |
US5522924A (en) | 1995-03-17 | 1996-06-04 | Ecc International Inc. | Method for producing high brightness low abrasion calcined kaolin pigment |
US5600043A (en) | 1995-03-27 | 1997-02-04 | The Geon Company | Oxychlorination process |
US5648508A (en) | 1995-11-22 | 1997-07-15 | Nalco Chemical Company | Crystalline metal-organic microporous materials |
US5856397A (en) | 1996-11-12 | 1999-01-05 | Ecc International Inc. | Dry grinding aid for dry milling a calcined kaolin clay and a related method |
US6495487B1 (en) * | 1996-12-09 | 2002-12-17 | Uop Llc | Selective bifunctional multimetallic reforming catalyst |
US6740373B1 (en) | 1997-02-26 | 2004-05-25 | Fort James Corporation | Coated paperboards and paperboard containers having improved tactile and bulk insulation properties |
DE19718871A1 (de) | 1997-05-03 | 1998-11-12 | Krupp Uhde Gmbh | Verfahren zur Oxichlorierung von Ethylen in einem Wirbelschicht-Katalysatorbett |
US5968250A (en) | 1997-06-06 | 1999-10-19 | Engelhard Corporation | Kaolin composition for use electrodeposition paints |
US6103005A (en) | 1997-06-20 | 2000-08-15 | Imerys Kaolin, Inc. | Compositions of large particle calcined kaolin clay and methods of making the same |
EP0931587A1 (en) | 1998-01-08 | 1999-07-28 | Evc Technology Ag | Catalyst, process for its preparation, and its use in the synthesis of 1,2-dichloroethane |
DE19812468A1 (de) | 1998-03-23 | 1999-09-30 | Basf Ag | Verfahren zur Herstellung von 1,2-Dichlorethan |
JPH11292805A (ja) | 1998-04-06 | 1999-10-26 | Mitsui Chem Inc | 炭化水素のオキシクロリネーション反応方法 |
JPH11292803A (ja) | 1998-04-06 | 1999-10-26 | Mitsui Chem Inc | エチレンのオキシクロリネーション方法 |
JPH11292804A (ja) | 1998-04-06 | 1999-10-26 | Mitsui Chem Inc | エチレンのオキシクロリネーション反応方法 |
US5997626A (en) | 1998-05-01 | 1999-12-07 | Engelhard Corporation | Low abrasion calcined kaolin pigments and enhanced filtration method |
DK1002576T3 (da) | 1998-11-10 | 2004-04-13 | Sued Chemie Mt Srl | Kobberbaseret katalysator til oxychlorering af ethylen til 1,2-dichlorethan |
US6136086A (en) | 1998-11-19 | 2000-10-24 | Englehard Corporation | Low sheen opacifying pigments and manufacture thereof by calcination of kaolin clay |
IT1306194B1 (it) * | 1999-01-08 | 2001-05-30 | Sued Chemie Mt Srl | Catalizzatori per reazioni esotermiche su letto fisso. |
US6680415B1 (en) * | 1999-11-22 | 2004-01-20 | Dow Global Technologies Inc. | Oxyhalogenation process using catalyst having porous rare earth halide support |
US6797845B1 (en) | 1999-11-22 | 2004-09-28 | Dow Global Technologies Inc. | Process for vinyl chloride manufacture from ethane and ethylene with immediate HCl recovery from reactor effluent |
JP2001226172A (ja) * | 2000-02-18 | 2001-08-21 | Mizusawa Ind Chem Ltd | アルミナ系成形体 |
US6379452B1 (en) | 2000-03-23 | 2002-04-30 | Thiele Kaolin Company | Calcined kaolin clay pigments having improved color and process for the manufacture thereof |
AU9297101A (en) | 2000-09-22 | 2002-04-02 | Engelhard Corp | Structurally enhanced cracking catalysts |
US6942784B2 (en) | 2000-09-22 | 2005-09-13 | Engelhard Corporation | Structurally enhanced cracking catalysts |
EP1199338A3 (en) | 2000-10-17 | 2004-01-21 | Imerys Kaolin, Inc. | Calcined kaolin pigments having improved combination of physical and applied properties, their production and use |
US6585822B2 (en) | 2001-01-05 | 2003-07-01 | Engelhard Corporation | Kaolin clay glossing pigment and preparation thereof |
ITMI20012241A1 (it) | 2001-10-25 | 2003-04-25 | Sued Chemie Mt Srl | Catalizzatori per l'ossiclorurazione dell'etilene a 1,2-dicloroetano |
TWI255736B (en) * | 2002-02-05 | 2006-06-01 | Basf Ag | A catalyst composition for the oxychlorination of ethylene and its use |
US7101473B2 (en) * | 2002-05-31 | 2006-09-05 | Engelhard Corporation | Method of enhancing the activity of FCC catalysts |
ITMI20030630A1 (it) | 2003-03-31 | 2004-10-01 | Sued Chemie Mt Srl | Catalizzatori per ossiclorurazione dell'etilene a 1,2-dicloroetano. |
US8298986B2 (en) * | 2005-12-12 | 2012-10-30 | Georgia Tech Research Corporation | Structures for capturing CO2, methods of making the structures, and methods of capturing CO2 |
US7795175B2 (en) * | 2006-08-10 | 2010-09-14 | University Of Southern California | Nano-structure supported solid regenerative polyamine and polyamine polyol absorbents for the separation of carbon dioxide from gas mixtures including the air |
-
2006
- 2006-11-09 TW TW095141560A patent/TWI341218B/zh active
- 2006-11-10 WO PCT/US2006/060758 patent/WO2007059424A1/en active Application Filing
- 2006-11-10 US US11/558,449 patent/US7585806B2/en active Active
- 2006-11-10 KR KR1020087013128A patent/KR100995947B1/ko active IP Right Grant
- 2006-11-10 AT AT06839813T patent/ATE540755T1/de active
- 2006-11-10 ES ES06839813T patent/ES2378084T3/es active Active
- 2006-11-10 JP JP2008540355A patent/JP2009515684A/ja active Pending
- 2006-11-10 MY MYPI20081608A patent/MY155020A/en unknown
- 2006-11-10 EP EP06839813A patent/EP1948358B1/en active Active
- 2006-11-10 BR BRPI0618386A patent/BRPI0618386B1/pt active IP Right Grant
- 2006-11-10 ZA ZA200804040A patent/ZA200804040B/xx unknown
- 2006-11-10 PL PL06839813T patent/PL1948358T3/pl unknown
- 2006-11-10 CN CN2006800501348A patent/CN101351266B/zh active Active
- 2006-11-10 UA UAA200808031A patent/UA95620C2/ru unknown
- 2006-11-10 KR KR1020107016928A patent/KR101164542B1/ko active IP Right Grant
- 2006-11-10 RU RU2008123602/04A patent/RU2387479C2/ru active
- 2006-11-14 AR ARP060104971A patent/AR057572A1/es active IP Right Grant
-
2008
- 2008-04-14 EG EG2008040608A patent/EG25821A/xx active
- 2008-04-14 NO NO20081814A patent/NO338431B1/no unknown
-
2009
- 2009-08-10 US US12/538,163 patent/US8956993B2/en active Active
Also Published As
Publication number | Publication date |
---|---|
KR20080075510A (ko) | 2008-08-18 |
US20090298682A1 (en) | 2009-12-03 |
KR100995947B1 (ko) | 2010-11-22 |
PL1948358T3 (pl) | 2012-06-29 |
BRPI0618386A2 (pt) | 2012-05-08 |
US20070112235A1 (en) | 2007-05-17 |
US8956993B2 (en) | 2015-02-17 |
ES2378084T3 (es) | 2012-04-04 |
KR20100092065A (ko) | 2010-08-19 |
WO2007059424B1 (en) | 2007-07-19 |
JP2009515684A (ja) | 2009-04-16 |
CN101351266B (zh) | 2012-12-26 |
MY155020A (en) | 2015-08-28 |
TW200735961A (en) | 2007-10-01 |
CN101351266A (zh) | 2009-01-21 |
RU2008123602A (ru) | 2009-12-27 |
US7585806B2 (en) | 2009-09-08 |
EP1948358A1 (en) | 2008-07-30 |
KR101164542B1 (ko) | 2012-07-11 |
UA95620C2 (ru) | 2011-08-25 |
TWI341218B (en) | 2011-05-01 |
ATE540755T1 (de) | 2012-01-15 |
NO338431B1 (no) | 2016-08-15 |
NO20081814L (no) | 2008-08-14 |
EP1948358B1 (en) | 2012-01-11 |
RU2387479C2 (ru) | 2010-04-27 |
ZA200804040B (en) | 2009-10-28 |
WO2007059424A1 (en) | 2007-05-24 |
EG25821A (en) | 2012-08-23 |
BRPI0618386B1 (pt) | 2016-05-17 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
AR057572A1 (es) | Composiciones de catalizador y proceso para oxicloracion | |
Iqbal et al. | Chemical design of palladium‐based nanoarchitectures for catalytic applications | |
Fu et al. | Active sites of Pd-doped flat and stepped Cu (111) surfaces for H2 dissociation in heterogeneous catalytic hydrogenation | |
Xu et al. | Recent advances in solar‐driven CO2 reduction over g‐C3N4‐based photocatalysts | |
Kang et al. | Synthesis of porous palladium superlattice nanoballs and nanowires | |
Wang et al. | Ionic liquid-employed synthesis of Bi2E3 (E= S, Se, and Te) hierarchitectures: The case of Bi2S3 with superior visible-light-driven Cr (VI) photoreduction capacity | |
Ali et al. | Enhanced hydrogen generation via overall water splitting using novel MoS2-BN nanoflowers assembled TiO2 ternary heterostructures | |
FR2826646B1 (fr) | Procede de fabrication selective de nanotubes de carbone ordonne en lit fluidise | |
TW200743667A (en) | Reforming nanocatalysts and methods of making and using such catalysts | |
BRPI0519002A2 (pt) | reforma de nanocatalisadores e mÉtodo de produÇço e utilizaÇço de tais catalisadores | |
Pennington et al. | Photocatalytic CO oxidation over nanoparticulate Au-modified TiO2 aerogels: the importance of size and intimacy | |
Qiu et al. | Bismuth nano-flowers as a highly selective catalyst for electrochemical reduction of CO2 to formate | |
Allaedini et al. | Synthesis of Fe–Ni–Ce trimetallic catalyst nanoparticles via impregnation and co-precipitation and their application to dye degradation | |
JP2009526659A5 (es) | ||
RU2001129280A (ru) | Катализатор для гидродехлорирования четыреххлористого углерода в хлороформ, способ получения катализатора и способ гидродехлорирования водородом четыреххлористого углерода в хлороформ | |
Jabbari et al. | Enhanced charge carrier efficiency and solar light-induced photocatalytic activity of TiO2 nanoparticles through doping of silver nanoclusters and C–N–S nonmetals | |
Li et al. | Fabrication, physicochemical properties and photocatalytic activity of Ag0. 68V2O5 hierarchical architecture assembled by ultrathin nanosheets | |
EP2864253B1 (en) | Method for obtaining oxide catalysts on the base of exfoliated layered aluminosilicates | |
Feng et al. | A DFT Study on the Catalytic CO Oxidative Coupling to Dimethyl Oxalate on Al-Doped Core–Shell Pd Clusters | |
Aronovitch et al. | Stability of seeded rod photocatalysts: atomic scale view | |
García-Dalí et al. | Molecular functionalization of 2H-Phase MoS2 nanosheets via an electrolytic route for enhanced catalytic performance | |
Werdinius et al. | Nanofabrication of planar model catalysts by colloidal lithography: Pt/ceria and Pt/alumina | |
Zámbó et al. | One‐Step Formation of Hybrid Nanocrystal Gels: Deposition of Metal Domains on CdSe/CdS Nanorod and Nanoplatelet Networks | |
JP6192042B2 (ja) | カーボンナノチューブ集合体及びその製造方法 | |
Dıaz-Ballote et al. | Activity of SiC particles in Al-based metal matrix composites revealed by SECM |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FG | Grant, registration |