GB911246A - Improvements in and relating to hydration and dehydration processes and to catalyststherefor - Google Patents
Improvements in and relating to hydration and dehydration processes and to catalyststhereforInfo
- Publication number
- GB911246A GB911246A GB15718/60A GB1571860A GB911246A GB 911246 A GB911246 A GB 911246A GB 15718/60 A GB15718/60 A GB 15718/60A GB 1571860 A GB1571860 A GB 1571860A GB 911246 A GB911246 A GB 911246A
- Authority
- GB
- United Kingdom
- Prior art keywords
- alumina
- thoria
- hydration
- catalysts
- phenol
- 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
- B01J23/12—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of actinides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C37/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring
- C07C37/01—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by replacing functional groups bound to a six-membered aromatic ring by hydroxy groups, e.g. by hydrolysis
- C07C37/055—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by replacing functional groups bound to a six-membered aromatic ring by hydroxy groups, e.g. by hydrolysis the substituted group being bound to oxygen, e.g. ether group
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Hydration-dehydration catalysts comprising thoria supported on a -alumina. are prepared by treating a -alumina in the solid phase to produce a deposit of thoria in its pores. They are suitable for catalysing the hydration of diphenyl oxides to the corresponding phenol or phenols as well as the reverse dehydration. They may be prepared by impregnating a -alumina which may be pelleted, with a solution of a thorium salt, e.g. the nitrate, and converting the salt to thoria; alternatively the alumina may be impregnated by teating it in aqueous suspension with a solution of a thorium salt. In this case it is preferably treated with ammonia to precipitate thorium hydroxide which is then converted by heating to thoria. Catalysts are preferred which contain about 25% thoria by weight of the alumina and which are in the form of pellets. The a -alumina may be obtained by firing alumina for 6 hours at 1000-1500 DEG C. The catalysts are regenerated by heating in a stream of air at 500 DEG C. The example describes the preparation and use of the catalysts.ALSO:The hydration of diphenyl oxides to a phenol or phenols and the corresponding dehydration is effected in the presence of a catalyst comprising thoria supported on a -alumina (see Group III). The reactions are preferably performed in the vapour phase at atmospheric pressure and elevated temperature, e.g. for diphenyl oxide itself 475 DEG C. The process may be carried out in successive cycles of reaction and regeneration, being accomplished by heating the catalyst in a stream of air at 500 DEG C. Specified reactants are diphenyl oxide, bis(p - methylphenyl)oxide, phenol p and p-cresol. In the example diphenyl oxide is converted to phenol.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB15718/60A GB911246A (en) | 1960-05-04 | 1960-05-04 | Improvements in and relating to hydration and dehydration processes and to catalyststherefor |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB15718/60A GB911246A (en) | 1960-05-04 | 1960-05-04 | Improvements in and relating to hydration and dehydration processes and to catalyststherefor |
Publications (1)
Publication Number | Publication Date |
---|---|
GB911246A true GB911246A (en) | 1962-11-21 |
Family
ID=10064236
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB15718/60A Expired GB911246A (en) | 1960-05-04 | 1960-05-04 | Improvements in and relating to hydration and dehydration processes and to catalyststherefor |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB911246A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0083140A1 (en) * | 1981-12-24 | 1983-07-06 | Stamicarbon B.V. | Process for the decarboxylative oxidation of a benzene monocarboxylic acid |
EP0317208A2 (en) * | 1987-11-16 | 1989-05-24 | Amoco Corporation | Preparation of Diaryl Ethers and Diaryl Sulfides |
US4978811A (en) * | 1988-04-01 | 1990-12-18 | The Dow Chemical Company | Process for hydrolysis of ortho-aromatic di-aryl ethers |
US5925798A (en) * | 1995-03-08 | 1999-07-20 | Solutia Inc. | Thoria catalyst |
-
1960
- 1960-05-04 GB GB15718/60A patent/GB911246A/en not_active Expired
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0083140A1 (en) * | 1981-12-24 | 1983-07-06 | Stamicarbon B.V. | Process for the decarboxylative oxidation of a benzene monocarboxylic acid |
EP0317208A2 (en) * | 1987-11-16 | 1989-05-24 | Amoco Corporation | Preparation of Diaryl Ethers and Diaryl Sulfides |
US4898982A (en) * | 1987-11-16 | 1990-02-06 | Amoco Corporation | Preparation of diaryl ethers and diaryl sulfides |
EP0317208A3 (en) * | 1987-11-16 | 1990-11-28 | Amoco Corporation | Preparation of diaryl ethers and diaryl sulfides |
US4978811A (en) * | 1988-04-01 | 1990-12-18 | The Dow Chemical Company | Process for hydrolysis of ortho-aromatic di-aryl ethers |
US5925798A (en) * | 1995-03-08 | 1999-07-20 | Solutia Inc. | Thoria catalyst |
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