GB998936A - Improvements in or relating to the production of conjugated diolefines - Google Patents
Improvements in or relating to the production of conjugated diolefinesInfo
- Publication number
- GB998936A GB998936A GB2010163A GB2010163A GB998936A GB 998936 A GB998936 A GB 998936A GB 2010163 A GB2010163 A GB 2010163A GB 2010163 A GB2010163 A GB 2010163A GB 998936 A GB998936 A GB 998936A
- Authority
- GB
- United Kingdom
- Prior art keywords
- oxide composition
- iron
- methylbutene
- butene
- mono
- 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
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
- 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
- B01J23/84—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 arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- B01J23/843—Arsenic, antimony or bismuth
- B01J23/8435—Antimony
-
- 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
- B01J23/005—Spinels
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C5/00—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
- C07C5/42—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with a hydrogen acceptor
- C07C5/48—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with a hydrogen acceptor with oxygen as an acceptor
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)
- Catalysts (AREA)
Abstract
Conjugated diolefines are prepared by reacting a mono-olefin containing not less than 4 carbon atoms in the vapour phase with molecular oxygen over an oxide composition containing antimony and iron as oxidation catalyst. The oxide composition may be a mixture of the metal oxides or a compound containing both metals, i.e. iron antimonate. The compositions are prepared (1) by mixing the metal oxides or compounds, e.g. hydroxides, nitrates and basic nitrate which on heating give the oxides, (2) by mixing antimony and iron salts, neutralizing the mixture with ammonia and recovering the precipitate. Catalyst activity is increased by preheating the oxide composition to 500 DEG to 1100 DEG C. and the oxide composition may be on a support, e.g. silica. Mono-olefine used are butene-1, butene-2, 3-methylbutene-1 and 2-methylbutene-2 and these may be present in amounts of 1% to 25% by volume of the feed gas which may also contain 1 to 21% by volume of oxygen and a diluent, e.g. nitrogen or steam. The reaction takes place at below 550 DEG C. with a contact time of 1 to 30 seconds. Sub, normal and superatmospheric pressure are used and fixed and fluid bed reactors are employed. The products, e.g. butadiene or isoprene may be recovered by solvent extraction or condensation followed by fractionation. Specification 902,952 is referred to.
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2010163A GB998936A (en) | 1963-05-21 | 1963-05-21 | Improvements in or relating to the production of conjugated diolefines |
DE19641443733 DE1443733A1 (en) | 1963-05-21 | 1964-05-12 | Process for making conjugated diolefins |
FR975100A FR1394625A (en) | 1963-05-21 | 1964-05-20 | Process for the production of conjugated diolefins |
NL6405673A NL6405673A (en) | 1963-05-21 | 1964-05-21 | |
BE648238A BE648238A (en) | 1963-05-21 | 1964-05-21 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2010163A GB998936A (en) | 1963-05-21 | 1963-05-21 | Improvements in or relating to the production of conjugated diolefines |
Publications (1)
Publication Number | Publication Date |
---|---|
GB998936A true GB998936A (en) | 1965-07-21 |
Family
ID=10140404
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2010163A Expired GB998936A (en) | 1963-05-21 | 1963-05-21 | Improvements in or relating to the production of conjugated diolefines |
Country Status (4)
Country | Link |
---|---|
BE (1) | BE648238A (en) |
DE (1) | DE1443733A1 (en) |
GB (1) | GB998936A (en) |
NL (1) | NL6405673A (en) |
-
1963
- 1963-05-21 GB GB2010163A patent/GB998936A/en not_active Expired
-
1964
- 1964-05-12 DE DE19641443733 patent/DE1443733A1/en active Pending
- 1964-05-21 BE BE648238A patent/BE648238A/xx unknown
- 1964-05-21 NL NL6405673A patent/NL6405673A/xx unknown
Also Published As
Publication number | Publication date |
---|---|
NL6405673A (en) | 1964-11-23 |
BE648238A (en) | 1964-11-23 |
DE1443733A1 (en) | 1968-11-21 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US3825502A (en) | Olefin oxidation catalyst | |
US3450788A (en) | Dehydrogenation process | |
US3328478A (en) | Production of conjugated diolefines by oxidative dehydrogenation | |
US2260409A (en) | Preparation of maleic acid | |
GB903034A (en) | The production of acrylic and methacrylic acids | |
US2326258A (en) | Production of butadiene | |
US3966823A (en) | Process for preparing 1,3-butadiene and methacrolein simultaneously | |
BR0113310B1 (en) | catalyst composition for the manufacture of acrylonitrile, and process for converting an olefin. | |
GB973338A (en) | An improved catalytic process for the preparation of methacrylonitrile | |
US3542842A (en) | Ammoxidation of propylene or isobutylene to acrylonitrile or methacrylonitrile | |
US3917682A (en) | Production of acetic acid by oxidation of butenes | |
US3218368A (en) | Process for the preparation of unsaturated hydrocarbons | |
US3544616A (en) | Ammoxidation of propylene or isobutylene to acrylonitrile or methacrylonitrile | |
GB998936A (en) | Improvements in or relating to the production of conjugated diolefines | |
US3666822A (en) | Uranium-molybdenum oxidation catalysts | |
US1895516A (en) | Catalytic process of producing ketones | |
US3424781A (en) | Production of unsaturated aliphatic nitriles | |
US3346659A (en) | Production of conjugated diolefines | |
US3251899A (en) | Process for the dehydrogenation of olefins | |
GB1065552A (en) | Process for the production of acrylonitrile | |
US3067272A (en) | Catalytic dehydrogenation process | |
US4075122A (en) | Catalyst and method of oxydehydrogenation of alkyl aromatic compounds | |
US3960925A (en) | Production of acrylonitrile by ammoxidation of propylene | |
US3259652A (en) | Oxidation of acrolein or methacrolein to the corresponding acid in the presence of an sn-sb-mo catalyst | |
US3398199A (en) | Process and catalyst for the oxidation of olefins |