WO2003066214A2 - Katalysatorzusammensetzung zur oxichlorierung - Google Patents

Katalysatorzusammensetzung zur oxichlorierung Download PDF

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Publication number
WO2003066214A2
WO2003066214A2 PCT/EP2003/001093 EP0301093W WO03066214A2 WO 2003066214 A2 WO2003066214 A2 WO 2003066214A2 EP 0301093 W EP0301093 W EP 0301093W WO 03066214 A2 WO03066214 A2 WO 03066214A2
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WIPO (PCT)
Prior art keywords
metal
catalyst
catalyst composition
composition according
salt
Prior art date
Legal status (The legal status 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 status listed.)
Ceased
Application number
PCT/EP2003/001093
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German (de)
English (en)
French (fr)
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WO2003066214A3 (de
Inventor
Christian Kuhrs
Ruprecht Meissner
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BASF SE
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BASF SE
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
Priority claimed from DE2002104608 external-priority patent/DE10204608A1/de
Priority claimed from DE2002136254 external-priority patent/DE10236254A1/de
Priority to US10/502,056 priority Critical patent/US7126035B2/en
Application filed by BASF SE filed Critical BASF SE
Priority to EP03704531A priority patent/EP1474233A2/de
Priority to JP2003565632A priority patent/JP4121459B2/ja
Priority to AU2003206831A priority patent/AU2003206831A1/en
Priority to KR1020047012024A priority patent/KR100976897B1/ko
Publication of WO2003066214A2 publication Critical patent/WO2003066214A2/de
Publication of WO2003066214A3 publication Critical patent/WO2003066214A3/de
Anticipated expiration legal-status Critical
Priority to US11/499,666 priority patent/US7902411B2/en
Ceased legal-status Critical Current

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    • 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
    • B01J23/89—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with noble metals
    • 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
    • B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/02—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the alkali- or alkaline earth metals or beryllium
    • 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
    • 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C17/00—Preparation of halogenated hydrocarbons
    • C07C17/013—Preparation of halogenated hydrocarbons by addition of halogens
    • C07C17/02—Preparation of halogenated hydrocarbons by addition of halogens to unsaturated 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
    • B01J21/00—Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
    • B01J21/02—Boron or aluminium; Oxides or hydroxides thereof
    • B01J21/04—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
    • B01J23/89—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with noble metals
    • B01J23/8933—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with noble metals also combined with metals, or metal oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
    • B01J23/8946—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with noble metals also combined with metals, or metal oxides or hydroxides provided for in groups B01J23/02 - B01J23/36 with alkali or alkaline earth metals
    • 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
    • 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
    • B01J35/63—Pore volume
    • B01J35/633—Pore volume less than 0.5 ml/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
    • B01J35/63—Pore volume
    • B01J35/635—0.5-1.0 ml/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
    • B01J37/00—Processes, in general, for preparing catalysts; Processes, in general, for activation of catalysts
    • B01J37/02—Impregnation, coating or precipitation
    • B01J37/0201—Impregnation

Definitions

  • the invention further relates to a process for the preparation of 1,2 dichloroethane by oxychlorination of ethylene, characterized by the reaction of a mixture of ethylene, oxygen or oxygen-containing gas and hydrogen chloride to 1,2-dichloroethane by means of a catalyst of the above composition.
  • Oxychlorination of ethylene to 1,2-dichloroethane is a well known process in which ethylene is reacted with hydrogen chloride and oxygen or with an oxygen-containing gas (e.g. air) in the gas phase and usually in the presence of a catalyst.
  • Suitable catalysts generally contain as a catalytically active component a copper compound which has been deposited on a carrier substance, preferably copper chloride on a carrier substance.
  • the supported catalysts used therefore usually contain what are known as promoters, by means of which the effectiveness of catalytically active copper chloride on supported substances is improved.
  • promoters include alkali metal chlorides, in particular potassium chloride and cesium chloride, alkaline earth metal chlorides, in particular magnesium chloride, or else chlorides of rare earth metals, in particular cerium chloride.
  • alkali metal chlorides in particular potassium chloride and cesium chloride
  • alkaline earth metal chlorides in particular magnesium chloride
  • chlorides of rare earth metals in particular cerium chloride.
  • EP-A 0 582 165 describes a catalyst composition comprising a support which has an active metal composition which contains 2 to 8% by weight of copper as copper chloride, 0.2 to 2% by weight of an alkali metal, 0.1 to 9 wt .-% of a rare earth metal and 0.05 to 4 wt .-% of a metal from group ILA of the periodic table (alkaline earth metals).
  • EP-A 0 375 202 discloses a catalyst composition for oxychlorination, comprising a mixture of metal chlorides on a support, which essentially contains a mixture of copper chloride, magnesium chloride and potassium chloride in such proportions that the catalyst composition 3 to 9% by weight of copper, 0.2 to 3% by weight of magnesium and 0.2 to 3% by weight of potassium.
  • the selectivity with which ethylene is converted in the oxychlorination reaction into the desired end product 1,2-dichloroethane - and not into the by-products customary in oxychlorination - is strongly dependent on the catalyst composition used. Especially in reactions with high ethylene conversion, too many by-products are still obtained when using the catalyst compositions which have been customary to date.
  • Fluidized bed catalysts for the oxychlorination of ethylene to 1,2-dichloroethane must therefore not only be optimized in terms of activity and selectivity, but also have a "sticking" -free swirl behavior. It can be observed that copper-rich catalysts have a greater tendency to stick together than low-copper catalysts.
  • a catalyst composition for the oxychlorination of ethylene comprising a mixture of metal salts on a support, said metal salts being applied to the support in such proportions that the catalyst composition
  • % preferably 0.005 to 0.05% by weight, of at least one metal selected from the group consisting of ruthenium, rhodium, palladium, osmium, iridium and platinum and / or 0.0001 to 0.1% by weight, preferably 0.001 to 0.05% by weight of gold, as a corresponding metal salt or tetrachlorogoldic acid, comprises, wherein all weight percentages are based on the total weight of the catalyst including support material.
  • the presence of small amounts of a salt of the platinum metals, which include ruthenium, rhodium, palladium, osmium, iridium and platinum, or the presence of small amounts of corresponding gold compounds in the catalyst composition used increase the conversion of the starting materials ethylene and hydrogen chloride significantly, but without to reduce the selectivity for the formation of 1,2 dichloroethane. This ultimately results in a higher yield of 1,2 dichloroethane.
  • the fluidization behavior is not influenced by the addition of small amounts of the metal salts mentioned above.
  • the corresponding oxyhalides, the oxides or the halides of the platinum metals or gold, in particular the chlorides of the platinum metals or gold are preferably used as the metal salts of the platinum metals or gold.
  • ruthenium salt in particular the presence of ruthenium chloride, in the quantitative ratio defined above in the catalyst composition is further preferred.
  • a gold salt in particular of gold chloride or tetrachlorogoldic acid, in the quantitative ratio defined above in the catalyst composition is particularly preferred.
  • CO and CO 2 are in a ratio of approximately 1: 1 to each other.
  • Circulation reactor processes are these by-products of oxychlorination
  • Aluminum oxide, silica gel, pumice stone and clay can be used as the carrier substance for the catalyst composition according to the invention.
  • the use of aluminum oxide as the carrier substance is preferred.
  • the specific surface area of the carrier substance before the metal salt deposition is preferably in the range from 20 to 400 m 2 / g, more preferably 75 to 200 m Ig.
  • Common carrier substances for oxychlorination catalysts preferably have pore volumes in the range from 0.15 to 0.75 cm 3 / g, and the average particle sizes are preferably in the range from 30 to 500 ⁇ m.
  • the proportion of particles with a diameter smaller than 45 ⁇ m is 30% or 5%, the BET surfaces being 170 m 2 / g or 150 m 2 / g.
  • the invention further relates to a process for the preparation of 1,2 dichloroethane for the oxychlorination of ethylene with catalysis of a catalyst composition according to the invention.
  • Ethylene, hydrogen chloride and molecular oxygen are brought into contact with a catalyst composition according to the invention at temperatures from 80 to 300 ° C., preferably at 210 to 260 ° C. in the gas phase.
  • the molecular oxygen can be used as such or in the form of an oxygen-containing gas mixture, e.g. Air to be discharged.
  • an oxygen-containing gas mixture e.g. Air to be discharged.
  • the molar ratios of the starting materials used in the process according to the invention are generally 5: 1 to 3: 1 for hydrogen chloride: oxygen, preferably approximately 4: 1 and generally approximately 1: 2 for ethylene: hydrogen chloride.
  • Hydrogen chloride based on the reaction 2 C 2 H 4 + 4 HC1 + O 2 a 2 C 2 H 4 CI 2 + 2 H 2 O, in slightly sub-stoichiometric amount, so that it is ensured that hydrogen chloride is converted almost completely in one reactor run.
  • ethylene is run in an even greater excess.
  • the ratio of ethylene: HCl: O 2 is preferably chosen so that ethylene is also converted as far as possible in one reactor pass.
  • the reaction pressure is in the range from 1 to 20 bar, preferably from 1 to 8 bar.
  • the reactor material used is usually based on iron (stainless steel) or based on a nickel alloy.
  • glass can also be used as the reactor material.
  • the catalyst can be used in the process according to the invention both as a fixed bed and as a fluidized bed. If the catalyst is used as a fluidized bed in the process according to the invention, it is preferably in the fluid state. This generally occurs at speeds in the range of 1 to 100 cm / s. If the catalyst is used as a fixed bed in the process according to the invention, it is preferably used in the form of hollow cylinders or ring tablets, the end faces of which are rounded off both towards the outer edge and towards the edge of the inner bores.
  • This preferably used fixed bed catalyst form is either hollow cylinders or ring tablets made up of catalytically active material, preferably a carrier material shaped into hollow cylinders or ring tablets, to which a catalytically active composition is applied.
  • the outside diameter of the hollow catalyst cylinder or ring tablets is 3 to 20 mm, preferably 3 to 10 mm, particularly preferably 3 to 7 mm, in particular 3.5 to 6.5 mm, and the inside diameter is 0.1 to 0 , 7 times the outer diameter.
  • the length of the hollow catalyst cylinder or ring tablets is 0.2 to 2 times, preferably 0.3 to 1.8 times, particularly preferably 0.4 to 1.6 times the outer diameter.
  • the radius of curvature of the end faces is 0.01 to 0.5 times, preferably 0.05 to 0.4 times, particularly preferably 0.1 to 0.2 times the outer diameter.
  • EP 1 127 618 AI Fixed bed catalysts of a form as described in EP 1 127 618 AI are thus an integral part of the present invention and are incorporated by reference.
  • the invention further relates to a process for the preparation of 1,2 dichloroethane by oxychlorination of ethylene with catalysis of a fixed bed catalyst with a composition according to the invention and optionally a form according to EP 1 127 618 AI.
  • aqueous solution for impregnating the carrier substance To prepare an aqueous solution for impregnating the carrier substance, the required amounts of the suitable metal compounds, preferably in the form of their hydrates, are dissolved in water. The aqueous solution is then applied to the carrier substance. The carrier substance impregnated in this way is then, if appropriate, filtered off from the remaining aqueous phase and finally dried. Filtration is not necessary if the carrier substance is brought into contact with a volume fraction of the aqueous solution which is not greater than is sufficient to saturate the carrier substance.
  • a catalyst composition according to the invention was prepared by impregnating the carrier substance with an aqueous solution, which was obtained as follows:
  • a catalyst composition was prepared in the same way with the same proportions by weight of copper chloride, magnesium chloride and potassium chloride, but without ruthenium chloride (catalyst B). Both oxychlorination catalysts (catalysts A and B) were used in a fluidized bed reactor made of glass, to which the starting materials ethylene, air and hydrogen chloride were fed and which was kept at 232 ° C., 243 ° C. and 254 ° C. bed temperature. The reactor was operated at a pressure of 4 bar with an amount of 500 g of the catalyst of the corresponding composition.
  • a further catalyst composition according to the invention was produced in accordance with Example 1, but instead of ruthenium chloride, palladium chloride was used as a promoter to produce catalyst C with 4.5% by weight Cu, 1.5% by weight Mg, 0.4% by weight K and To obtain 0.01 wt .-% Pd.
  • a further catalyst composition according to the invention was prepared in accordance with Example 1, but instead of ruthenium chloride, gold chloride was used as a promoter to produce catalyst D with 4.5% by weight Cu, 1.5% by weight Mg, 0.4% by weight K and To obtain 0.005% by weight of Au.

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  • 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)
  • Catalysts (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
PCT/EP2003/001093 2002-02-05 2003-02-04 Katalysatorzusammensetzung zur oxichlorierung Ceased WO2003066214A2 (de)

Priority Applications (6)

Application Number Priority Date Filing Date Title
KR1020047012024A KR100976897B1 (ko) 2002-02-05 2003-02-04 옥시염화를 위한 촉매 조성물
AU2003206831A AU2003206831A1 (en) 2002-02-05 2003-02-04 Catalyst composition for oxychlorination
US10/502,056 US7126035B2 (en) 2002-02-05 2003-02-04 Catalyst composition for oxychlorination
EP03704531A EP1474233A2 (de) 2002-02-05 2003-02-04 Katalysatorzusammensetzung zur oxichlorierung
JP2003565632A JP4121459B2 (ja) 2002-02-05 2003-02-04 １，２−ジクロロエタンの製造方法
US11/499,666 US7902411B2 (en) 2002-02-05 2006-08-07 Catalyst composition for oxychlorination

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
DE10204608.5 2002-02-05
DE2002104608 DE10204608A1 (de) 2002-02-05 2002-02-05 Katalysatorzusammensetzung zur Oxychlorierung
DE10236254.8 2002-08-07
DE2002136254 DE10236254A1 (de) 2002-08-07 2002-08-07 Katalysatorzusammensetzung zur Oxychlorierung

Related Child Applications (2)

Application Number Title Priority Date Filing Date
US10502056 A-371-Of-International 2003-02-04
US11/499,666 Continuation US7902411B2 (en) 2002-02-05 2006-08-07 Catalyst composition for oxychlorination

Publications (2)

Publication Number Publication Date
WO2003066214A2 true WO2003066214A2 (de) 2003-08-14
WO2003066214A3 WO2003066214A3 (de) 2004-02-05

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PCT/EP2003/001093 Ceased WO2003066214A2 (de) 2002-02-05 2003-02-04 Katalysatorzusammensetzung zur oxichlorierung

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US (2) US7126035B2 (https=)
EP (2) EP1474233A2 (https=)
JP (2) JP4121459B2 (https=)
KR (1) KR100976897B1 (https=)
CN (1) CN1627989A (https=)
AU (1) AU2003206831A1 (https=)
RU (1) RU2004126865A (https=)
TW (1) TWI255736B (https=)
WO (1) WO2003066214A2 (https=)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2198958A1 (en) * 2008-12-17 2010-06-23 Süd Chemie - Catalysts Italia S.R.L. Catalysts for oxychlorination of ethylene to 1.2-dichloroethane
EP2208528A1 (en) * 2008-12-23 2010-07-21 Süd Chemie - Catalysts Italia S.R.L. Catalysts for fixed bed oxychlorination of ethylene to 1.2-dichloroethane

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2006119804A1 (en) * 2005-05-12 2006-11-16 Solvay (Societe Anonyme) Oxychlorination catalyst and process using such a catalyst
TWI341218B (en) * 2005-11-14 2011-05-01 Oxy Vinyls Lp Catalyst compositions and process for oxychlorination
US20100310441A1 (en) * 2009-06-05 2010-12-09 Basf Corporation Catalytic Article for Removal of Volatile Organic Compounds in Low Temperature Applications
CN102188975B (zh) * 2011-03-09 2013-01-23 浙江工业大学 一种负载型镍基双组分催化剂及其应用
RU2664799C2 (ru) * 2012-11-05 2018-08-22 Басф Корпорейшн Катализатор для оксихлорирования этилена до 1,2-дихлорэтана
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
CA2987508A1 (en) * 2015-05-28 2016-12-01 Evolva Sa Biosynthesis of phenylpropanoids and phenylpropanoid derivatives
CN105126879B (zh) * 2015-07-15 2018-01-02 内蒙古大学 一种负载型钙钛矿乙烷氧氯化制氯乙烯催化剂的制备方法
CN108144632B (zh) * 2018-01-22 2020-11-03 西安元创化工科技股份有限公司 一种甲烷氧氯化的二氧化钌催化剂及其制备方法
KR102287846B1 (ko) * 2018-12-21 2021-08-06 한화솔루션 주식회사 염소 제조를 위한 염화수소 산화반응용 촉매 및 이의 제조방법
WO2022013751A1 (en) * 2020-07-14 2022-01-20 Sabic Global Technologies B.V. Catalysts for hydrogenation of aromatic containing polymers and uses thereof

Family Cites Families (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE206265C (https=)
NL134186C (https=) * 1963-10-07 1900-01-01
NL130969C (https=) * 1964-06-01 1900-01-01
IT958619B (it) * 1971-06-30 1973-10-30 Sumitomo Chemical Co Procedimento per preparare idrocarburi clorurati
JPS5312485B2 (https=) 1973-03-22 1978-05-01
ZA784827B (en) * 1977-09-06 1979-08-29 Ici Ltd Oxyhalogenation process
US4300005A (en) * 1977-12-02 1981-11-10 Monsanto Co. Preparation of vinyl chloride
US4446249A (en) * 1979-11-05 1984-05-01 The B. F. Goodrich Company Copper catalyst compositions for fluid-bed oxyhydrochlorination of ethylene
DE2949530A1 (de) * 1979-12-08 1981-06-11 Hoechst Ag, 6000 Frankfurt Verfahren zur herstellung von 1,2-dichlorethan
DE3522473A1 (de) * 1985-06-22 1987-01-02 Basf Ag Geformter katalysator, verfahren zu seiner herstellung und dessen verwendung bei der oxichlorierung von ethylen zu 1,2-dichlorethan
FR2600643B1 (fr) * 1986-06-27 1988-09-23 Solvay Procede d'oxychloration de l'ethylene et compositions catalytiques pour l'oxychloration
GB8829706D0 (en) 1988-12-20 1989-02-15 Ici Plc Oxychlorination catalyst composition
JP3092330B2 (ja) * 1992-06-30 2000-09-25 住友化学工業株式会社 オキシ塩素化触媒、その製造方法およびそれを用いるオキシ塩素化方法
US5292703A (en) 1992-07-28 1994-03-08 The Geon Company Catalyst and process for oxychlorination of ethylene to EDC
US5347046A (en) * 1993-05-25 1994-09-13 Engelhard Corporation Catalyst and process for using same for the preparation of unsaturated carboxylic acid esters
US6803342B1 (en) * 1993-12-08 2004-10-12 Solvay (Societe Anonyme) Catalytic composition and process for the oxychlorination of ethylene using such a composition
BE1007818A3 (fr) 1993-12-08 1995-10-31 Solvay Composition catalytique et procede d'oxychloration de l'ethylene utilisant une telle composition.
DE19645047A1 (de) * 1996-10-31 1998-05-07 Basf Ag Katalysatoren für die Aminierung von Alkylenoxiden, Alkoholen, Aldehyden und Ketonen
JPH11130702A (ja) * 1997-10-27 1999-05-18 Mitsui Chem Inc エチレンのオキシクロル化方法及びその反応装置
US6072078A (en) * 1997-12-12 2000-06-06 Celanese International Corporation Vinyl acetate production using a catalyst comprising palladium, gold, copper and any of certain fourth metals
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
DE10009017A1 (de) * 2000-02-25 2001-09-06 Basf Ag Geformte Katalysatoren
DE10024928A1 (de) * 2000-05-19 2001-11-22 Basf Ag Katalysatoren für heterogen katalysierte Reaktionen

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2198958A1 (en) * 2008-12-17 2010-06-23 Süd Chemie - Catalysts Italia S.R.L. Catalysts for oxychlorination of ethylene to 1.2-dichloroethane
EP2208528A1 (en) * 2008-12-23 2010-07-21 Süd Chemie - Catalysts Italia S.R.L. Catalysts for fixed bed oxychlorination of ethylene to 1.2-dichloroethane
US8216960B2 (en) 2008-12-23 2012-07-10 Sued-Chemie Catalysts Italia S.R.L. Catalysts for fixed bed oxychlorination of ethylene to 1.2-dichloroethane

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RU2004126865A (ru) 2006-02-10
TWI255736B (en) 2006-06-01
US7126035B2 (en) 2006-10-24
KR20040073610A (ko) 2004-08-19
KR100976897B1 (ko) 2010-08-18
US20050020864A1 (en) 2005-01-27
CN1627989A (zh) 2005-06-15
AU2003206831A8 (en) 2003-09-02
AU2003206831A1 (en) 2003-09-02
JP4741623B2 (ja) 2011-08-03
EP1474233A2 (de) 2004-11-10
WO2003066214A3 (de) 2004-02-05
TW200302752A (en) 2003-08-16
EP2314374A1 (de) 2011-04-27
JP2008194691A (ja) 2008-08-28
JP4121459B2 (ja) 2008-07-23
US7902411B2 (en) 2011-03-08
US20060270879A1 (en) 2006-11-30

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