GB781765A - Process for the manufacture of alkylene oxide condensation products - Google Patents
Process for the manufacture of alkylene oxide condensation productsInfo
- Publication number
- GB781765A GB781765A GB13620/54A GB1362054A GB781765A GB 781765 A GB781765 A GB 781765A GB 13620/54 A GB13620/54 A GB 13620/54A GB 1362054 A GB1362054 A GB 1362054A GB 781765 A GB781765 A GB 781765A
- Authority
- GB
- United Kingdom
- Prior art keywords
- reaction
- ethylene oxide
- reactor
- liquid
- oxide
- 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
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B61/00—Other general methods
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
Alkylene oxide condensation products are prepared by reaction of alkylene oxides in the vaporized state with organic or inorganic compounds containing at least one reactive hydrogen atom and in the form of a finely-divided liquid or solution in a circulatory apparatus in which the liquid reaction mixture is continuously withdrawn and recycled to the reactor, the alkylene oxide being evaporated outside the reaction zone and then introduced into the reaction zone in the form of vapour under substantially atmospheric pressure for reaction with the finely-divided second reagent. Specified reagents are carboxylic acids, amides, amines, mercaptans, hydroxy-compounds and sodium bisulphite, and ethylene, propylene and butylene oxides, preferably used without a diluent. Temperatures of 50-200 DEG C. are suitable and catalysts may be present. Suitable apparatus is described. Examples illustrate the reaction of octyl phenol with about 8 mols. of ethylene oxide, castor oil with about 15 mols. of ethylene oxide and aqueous sodium bisulphite with about one mol. of ethylene oxide. Specification 683,884 is referred to.ALSO:Alkylene oxide condensation products are prepared by reaction of alkylene oxides in a vaporized state with organic or inorganic compounds containing at least one active hydrogen atom and in the form of a finely divided liquid or of a finely divided solution in a circulatory apparatus in which the liquid reaction mixture is continuously withdrawn and recycled to the reactor, the alkylene oxide being evaporated outside the reaction zone and then continuously introduced into the reaction zone in the form of vapour under substantially atmospheric pressure for reaction with the finely divided droplets of the second reagent. Specified reagents are ethylene, propylene and butylene oxides, which are preferably used without a diluent, and carboxylic acids, amides, amines, mercaptans, hydroxy-compounds including alkyl-phenols and sodium bisulphite. Reaction temperatures of 50-200 DEG C. are suitable. Catalysts may be present. According to examples using illustrated apparatus (not shown) : (1) octyl-phenol containing added sodium as catalyst is heated in a vented cylindrical reactor to 150 DEG C. and the liquid phenol is continuously cycled by a pump from the base of the reactor to a centrifugal nozzle at the top; liquid ethylene oxide is fed to an evaporator and the vaporized oxide is then passed continuously into the top of the reactor at atmospheric pressure at a rate such that substantially no ethylene oxide gas escapes from the reactor vent; about 8 mols. of ethylene oxide are combined with 1 mol. of phenol; in like manner (2) castor oil is reacted with about 15 molar proportions of ethylene oxide; and (3) sodium bisulphite in aqueous solution with about one molar proportion of ethylene oxide. Specification 683,884 is referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH781765X | 1953-05-13 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB781765A true GB781765A (en) | 1957-08-28 |
Family
ID=4536286
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB13620/54A Expired GB781765A (en) | 1953-05-13 | 1954-05-10 | Process for the manufacture of alkylene oxide condensation products |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB781765A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3102893A (en) * | 1959-09-30 | 1963-09-03 | Monsanto Chemicals | Polyether-substituted glycidyl ethers |
US4385173A (en) | 1980-04-21 | 1983-05-24 | Shell Oil Company | Polyol polyether preparation process |
-
1954
- 1954-05-10 GB GB13620/54A patent/GB781765A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3102893A (en) * | 1959-09-30 | 1963-09-03 | Monsanto Chemicals | Polyether-substituted glycidyl ethers |
US4385173A (en) | 1980-04-21 | 1983-05-24 | Shell Oil Company | Polyol polyether preparation process |
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