GB686572A - Improvements in production of hydrogen peroxide - Google Patents
Improvements in production of hydrogen peroxideInfo
- Publication number
- GB686572A GB686572A GB26141/50A GB2614150A GB686572A GB 686572 A GB686572 A GB 686572A GB 26141/50 A GB26141/50 A GB 26141/50A GB 2614150 A GB2614150 A GB 2614150A GB 686572 A GB686572 A GB 686572A
- Authority
- GB
- United Kingdom
- Prior art keywords
- anthraquinone
- intermediary
- hydrogen peroxide
- production
- disclosed
- 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
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B15/00—Peroxides; Peroxyhydrates; Peroxyacids or salts thereof; Superoxides; Ozonides
- C01B15/01—Hydrogen peroxide
- C01B15/022—Preparation from organic compounds
- C01B15/023—Preparation from organic compounds by the alkyl-anthraquinone process
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
In the production of hydrogen peroxide wherein an alkylated anthraquinone intermediary is hydrogenated in solution in the presence of a catalyst to produce the corresponding anthrahydroquinone and the latter is oxidized to produce hydrogen peroxide and to regenerate the alkylated anthraquinone which is recycled, the anthraquinone intermediary is 2 tertiarybutyl anthraquinone, preferably in admixture with tetrahydro-2-tertiary-butylanthraquinone, for example 10-40 per cent thereof. A suitable solvent medium for the quinone and hydroquinone form of the intermediary is 25-75 per cent mixture by volume of primary or secondary nonyl alcohols such as di-isobutylcarbinol or 3.5.5 trimethylthexanol-1, and a mono or dimethyl naphthalene, particularly a methyl naphthalene, such solvents being disclosed in Specification 686,567. The reduction of the anthraquinone is preferably effected in the presence of activated alumina-supported palladium catalyst as disclosed in Specification 686,574. Hydrogenation temperature of 20 to 40 DEG C and oxidation temperatures of 30-60 DEG C may be employed. Specification 465,070 also is referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US686572XA | 1949-11-05 | 1949-11-05 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB686572A true GB686572A (en) | 1953-01-28 |
Family
ID=22083917
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB26141/50A Expired GB686572A (en) | 1949-11-05 | 1950-10-26 | Improvements in production of hydrogen peroxide |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB686572A (en) |
-
1950
- 1950-10-26 GB GB26141/50A patent/GB686572A/en not_active Expired
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