GB802100A - Selective hydrogenation of acetylene in ethylene - Google Patents

Selective hydrogenation of acetylene in ethylene

Info

Publication number
GB802100A
GB802100A GB62657A GB62657A GB802100A GB 802100 A GB802100 A GB 802100A GB 62657 A GB62657 A GB 62657A GB 62657 A GB62657 A GB 62657A GB 802100 A GB802100 A GB 802100A
Authority
GB
United Kingdom
Prior art keywords
acetylene
palladium
ethylene
hydrogen
silver
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.)
Expired
Application number
GB62657A
Inventor
Ludo Karl Frevel
Leonard Joseph Kressley
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Dow Chemical Co
Original Assignee
Dow Chemical Co
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 Chemical Co filed Critical Dow Chemical Co
Priority to GB62657A priority Critical patent/GB802100A/en
Publication of GB802100A publication Critical patent/GB802100A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C7/00Purification; Separation; Use of additives
    • C07C7/148Purification; Separation; Use of additives by treatment giving rise to a chemical modification of at least one compound
    • C07C7/163Purification; Separation; Use of additives by treatment giving rise to a chemical modification of at least one compound by hydrogenation
    • C07C7/167Purification; Separation; Use of additives by treatment giving rise to a chemical modification of at least one compound by hydrogenation for removal of compounds containing a triple carbon-to-carbon bond
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/38Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
    • B01J23/48Silver or gold
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/70Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
    • B01J23/89Catalysts 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
    • B01J23/8926Copper and noble metals

Abstract

A catalyst containing not more than 5 per cent by weight of a metallic mixture of 60 to 99 parts by weight of palladium and 40 to 1 part of copper, silver, or gold disposed on a catalytically inactive carrier such as pumice, inactive alumina, diatomaceous earth, asbestos, coke or charcoal, is used in the selective hydrogenation of acetylene in the presence of ethylene (see Group IV (b)). The catalysts are prepared by treating the support with aqueous solutions of soluble salts of the metals which salts can be decomposed at temperatures below 500 DEG C., drying the mixture, roasting in air at 325-500 DEG C. to convert the metal salts to the oxides and reducing to the metal in hydrogen at 25-450 DEG C. Specified salts are palladium nitrate, cupric nitrate, silver nitrate and chlorocuric acid. The catalysts are gradually inactivated by the deposition of carbonaceous matter and are readily reactivated by burning off the deposits by oxidation at, e.g., 400 DEG C., followed by reduction of the catalyst in hydrogen.ALSO:Acetylene is selectively hydrogenated in the presence of ethylene by contacting the mixture together with more than one mol. of hydrogen per mol. of acetylene with a catalyst containing a metallic mixture containing 60 to 99 parts by weight of palladium and 40 to 1 part of copper, silver or gold (see Group III). The feed is preferably desulphurized, e.g. by passing through basic lead acetate. Temperatures of room temperature to 250 DEG C. are used at above, below or at atmospheric pressure. A typical example illustrates the hydrogenation of acetylene in a gas stream produced from a commercial gas cracking plant consisting mostly of ethylene with small amounts of acetylene (3-4 volume per cent) methane, carbon dioxide and air. Hydrogen is added and the gas passed over a catalyst containing 0.2 per cent palladium and 0.01 per cent silver on diatomaceous earth at 100 DEG C. and 50 p.s.i.g.; the product stream is free of acetylene.
GB62657A 1957-01-07 1957-01-07 Selective hydrogenation of acetylene in ethylene Expired GB802100A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB62657A GB802100A (en) 1957-01-07 1957-01-07 Selective hydrogenation of acetylene in ethylene

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB62657A GB802100A (en) 1957-01-07 1957-01-07 Selective hydrogenation of acetylene in ethylene

Publications (1)

Publication Number Publication Date
GB802100A true GB802100A (en) 1958-10-01

Family

ID=9707651

Family Applications (1)

Application Number Title Priority Date Filing Date
GB62657A Expired GB802100A (en) 1957-01-07 1957-01-07 Selective hydrogenation of acetylene in ethylene

Country Status (1)

Country Link
GB (1) GB802100A (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2523149A1 (en) * 1982-03-15 1983-09-16 Catalyse Soc Prod Francais NEW CATALYST SUPPORTING PALLADIUM-OR, ITS PREPARATION AND USE IN SELECTIVE HYDROGENATION REACTIONS OF DIOLEFINIC AND / OR ACETYLENE HYDROCARBONS
EP1151790A1 (en) * 2000-04-30 2001-11-07 China Petro-Chemical Corporation Catalyst for selective hydrogenation, process for preparation of the same, its use in selectiv hydrogenation
US7521393B2 (en) 2004-07-27 2009-04-21 Süd-Chemie Inc Selective hydrogenation catalyst designed for raw gas feed streams
CN112191244A (en) * 2020-08-31 2021-01-08 浙江工业大学 Activated carbon-supported gold-based catalyst, preparation method thereof and application thereof in acetylene hydrogenation
CN113573808A (en) * 2019-09-30 2021-10-29 株式会社Lg化学 Catalyst for hydrogenation reaction and method for producing the same
CN113751010A (en) * 2020-06-05 2021-12-07 台州学院 Titanium dioxide loaded copper-gallium-indium liquid alloy catalyst and preparation method and application thereof
CN115739152A (en) * 2022-11-08 2023-03-07 中国科学院金属研究所 Non-noble metal catalyst Ni for selective hydrogenation of acetylene 3 CuN and preparation method and application thereof

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0089252A1 (en) * 1982-03-15 1983-09-21 Pro-Catalyse Supported palladium-gold catalyst, its preparation and its use in the selective hydrogenation of diolefinic and/or acetylenic hydrocarbons
US4490481A (en) * 1982-03-15 1984-12-25 Ste Francaise Des Produits Pour Catalyse Chez Institut Francais Du Petrole Supported palladium-gold catalyst, and its manufacture
FR2523149A1 (en) * 1982-03-15 1983-09-16 Catalyse Soc Prod Francais NEW CATALYST SUPPORTING PALLADIUM-OR, ITS PREPARATION AND USE IN SELECTIVE HYDROGENATION REACTIONS OF DIOLEFINIC AND / OR ACETYLENE HYDROCARBONS
EP1151790A1 (en) * 2000-04-30 2001-11-07 China Petro-Chemical Corporation Catalyst for selective hydrogenation, process for preparation of the same, its use in selectiv hydrogenation
US6627578B2 (en) 2000-04-30 2003-09-30 China Petro-Chemical Corporation Catalyst for selective hydrogenation
US7521393B2 (en) 2004-07-27 2009-04-21 Süd-Chemie Inc Selective hydrogenation catalyst designed for raw gas feed streams
US11872546B2 (en) 2019-09-30 2024-01-16 Lg Chem, Ltd. Catalyst for hydrogenation reaction and method for producing same
CN113573808A (en) * 2019-09-30 2021-10-29 株式会社Lg化学 Catalyst for hydrogenation reaction and method for producing the same
CN113573808B (en) * 2019-09-30 2024-04-16 株式会社Lg化学 Catalyst for hydrogenation reaction and method for producing same
CN113751010A (en) * 2020-06-05 2021-12-07 台州学院 Titanium dioxide loaded copper-gallium-indium liquid alloy catalyst and preparation method and application thereof
CN112191244A (en) * 2020-08-31 2021-01-08 浙江工业大学 Activated carbon-supported gold-based catalyst, preparation method thereof and application thereof in acetylene hydrogenation
CN112191244B (en) * 2020-08-31 2023-03-31 浙江工业大学 Activated carbon-supported gold-based catalyst, preparation method thereof and application thereof in acetylene hydrogenation
CN115739152A (en) * 2022-11-08 2023-03-07 中国科学院金属研究所 Non-noble metal catalyst Ni for selective hydrogenation of acetylene 3 CuN and preparation method and application thereof

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