GB396712A - Improvements in or relating to catalytic and like contact masses containing platinum - Google Patents

Improvements in or relating to catalytic and like contact masses containing platinum

Info

Publication number
GB396712A
GB396712A GB3601/32A GB360132A GB396712A GB 396712 A GB396712 A GB 396712A GB 3601/32 A GB3601/32 A GB 3601/32A GB 360132 A GB360132 A GB 360132A GB 396712 A GB396712 A GB 396712A
Authority
GB
United Kingdom
Prior art keywords
treated
platinum
carrier
mass
gel
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
GB3601/32A
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.)
Silica Gel Corp
Original Assignee
Silica Gel Corp
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 Silica Gel Corp filed Critical Silica Gel Corp
Publication of GB396712A publication Critical patent/GB396712A/en
Expired legal-status Critical Current

Links

Classifications

    • 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
    • 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
    • B01J23/40Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals of the platinum group metals
    • B01J23/42Platinum
    • 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
    • B01J23/54Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
    • B01J23/56Platinum group metals

Abstract

Catalysts for the oxidation of sulphur dioxide to sulphur trioxide comprise a carrier consisting of a dried hydrous oxide gel, such as silica gel, or a base-exchange compound, platinum introduced by impregnation and a promoter consisting of a compound of one or more of the metals iron, nickel, aluminium, copper, bismuth, molybdenum, beryllium, vanadium, tin, chromium or preferably manganese, in an amount up to 5 per cent by weight of the mass. The carrier may consist of one or more hydrous oxide gels, which includes both hydrogels and gelatinous precipitates or mixtures thereof. Suitable oxides are those of silicon, germanium, chromium, tungsten, titanium, aluminium or tin. The catalyst may be prepared in a variety of ways, for example, a carrier may be treated simultaneously or successively with a solution of a promoter substance and of a platinum compound and then treated to convert the platinum into metal; a carrier may be charged with a reacting gas such as hydrogen, hydrogen sulphide, carbon monoxide, arsine, phosphine, stibine, water gas, formaldehyde, or sulphur dioxide, then treated simultaneously or successively with a solution of a platinum compound and of a promoter substance and finally treated to obtain metallic platinum. The carrier may be first treated with the solutions and then with the reacting gas. The promoter substance may be incorporated in the carrier gel at any stage of its manufacture and the mass then treated with a platinum solution, either before or after drying, and then treated to form metallic platinum in the mass. This method is applicable when the promoter is a metal oxide such as alumina or stannia and can be incorporated in the form of a non-dehydrated hydrous oxide gel. A carrier including a non-dehydrated gel may be charged with a solution of a promoter substance, dried, and then treated with a platinum solution. The non-dehydrated gel may be one which when dried has a low apparent density and may be obtained by immersing any non-dehydrated gel in water at a temperature of 175-200 DEG F. for several hours. The carrier may also be treated with a platinum solution which is converted to metallic platinum and the mass is then treated with a solution of a promoter substance. If the platinum compound used is ammonium chloroplatinate, the mass is heated to about 360 DEG C., and if the platinum is present in the carrier as the sulphide after impregnation, the mass is heated in a stream of air at 500 DEG C. for about 4 hours. To obtain a rigid catalyst which will withstand rough usage, a reinforcing material may be incorporated at any stage in the preparation of the catalyst. The reinforcing substance may be any material which becomes plastic under suitable treatment and which when baked is changed into a non-plastic rigid solid. Suitable substances are clays containing a large percentage of aluminium silicate or aluminium and silica, e.g. Japanese clay, ball or fire clay, or mixtures thereof. The mass is preferably baked at temperatures from 800 DEG C. but not exceeding 900 DEG C. According to examples, the following catalytic masses are obtained by the methods described above. (1) A carrier of silica gel is mixed with a small amount of alumina gel, acting as a promoter, and the mass impregnated with platinum. (2) A carrier of silica gel impregnated with chromium oxide is treated with ammonium chloroplatinate. (3) and (4) In a similar catalyst, the promoter is manganese sulphate. (5) Silica gel is impregnated with aluminium sulphate and ammonium chloroplatinate and mixed with Japanese clay. The mass is ground, extruded, dried and baked. (6) Silica gel is impregnated with manganese sulphate and dried. The hard porous mass is then treated with ammonium chloroplatinate, which is converted to platinum sulphide and the mass heated to convert the sulphide to metallic platinum. (7) A gel of tungsten oxide is treated as in example (3). (8) A mixed gel of tungsten and tin oxides is dried and the hard porous mass treated with ammonium chloroplatinate and heated to obtain metallic platinum. The mass is treated with a solution of vanadyl sulphate and heated to obtain vanadium oxide. (9) A carrier consisting of dried titanium oxide gel of low apparent density is treated with a solution of aluminium chloride and ammonium chloroplatinate and heated. (10) Silica gel is charged with hydrogen sulphide and treated with a solution of platinic chloride and copper sulphate. The mass is dried and heated in air at 500 DEG C. to convert the sulphide into platinum and copper oxide. (11) A carrier including silica gel fines is treated with beryllium sulphate and ammonium chloroplatinate solutions and then heated. (12) A carrier containing a newly dehydrated base-exchange compound such as glauconite is treated as in example (11). Specifications 280,939, 286,708, and 314,858, [all in Class 1 (i), Chemical processes &c.], are referred to. The Specification as open to inspection under Sect. 91 comprises the use of a porous carrier generally and is not limited to the oxidation of sulphur dioxide to sulphur trioxide. This subject-matter does not appear in the Specification as accepted.
GB3601/32A 1931-02-07 1932-02-06 Improvements in or relating to catalytic and like contact masses containing platinum Expired GB396712A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US396712XA 1931-02-07 1931-02-07

Publications (1)

Publication Number Publication Date
GB396712A true GB396712A (en) 1933-08-08

Family

ID=21906746

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3601/32A Expired GB396712A (en) 1931-02-07 1932-02-06 Improvements in or relating to catalytic and like contact masses containing platinum

Country Status (1)

Country Link
GB (1) GB396712A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2496265A (en) * 1944-07-25 1950-02-07 Standard Oil Dev Co Hydrocarbon synthesis process
US2746937A (en) * 1951-05-01 1956-05-22 Exxon Research Engineering Co Process of preparing platinum-alumina hydroforming catalysts
US9375707B2 (en) 2007-08-30 2016-06-28 Solvay Sa Catalyst support and process for the preparation thereof

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2496265A (en) * 1944-07-25 1950-02-07 Standard Oil Dev Co Hydrocarbon synthesis process
US2746937A (en) * 1951-05-01 1956-05-22 Exxon Research Engineering Co Process of preparing platinum-alumina hydroforming catalysts
US9375707B2 (en) 2007-08-30 2016-06-28 Solvay Sa Catalyst support and process for the preparation thereof

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