GB733947A - Manufacture of bis-(ª‰-hydroxyalkyl-) polysulphides - Google Patents
Manufacture of bis-(ª‰-hydroxyalkyl-) polysulphidesInfo
- Publication number
- GB733947A GB733947A GB7686/53A GB768653A GB733947A GB 733947 A GB733947 A GB 733947A GB 7686/53 A GB7686/53 A GB 7686/53A GB 768653 A GB768653 A GB 768653A GB 733947 A GB733947 A GB 733947A
- Authority
- GB
- United Kingdom
- Prior art keywords
- polysulphide
- sulphur
- bis
- alkali
- sodium
- 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
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Polyethers (AREA)
Abstract
Bis - (b - hydroxyalkyl) polysulphides are prepared by reacting a 1,2-alkylene oxide with an alkali-metal polysulphide or alkaline-earth metal polysulphide in an aqueous medium and neutralizing the base liberated in the reaction as it is formed in such a manner that the reaction mixture does not become acid. Thus stoichiometric amounts of 1,2-alkylene oxide and of an alkali-binding substance may be introduced simultaneously into an aqueous solution of the alkali metal or alkaline earth metal polysulphide. Specified alkali-binding agents are sodium bicarbonate, buffer solutions containing acetates, borates, phosphates and the like, mineral acids and, preferably, carbon dioxide. The preferred reaction temperatures are from about 30 DEG to 90 DEG C. The alkylene oxide, which include ethylene, propylene and 3-hydroxy-propylene 1 : 2 oxides, may be used in gaseous or liquid form. It is preferred to employ a mixture of sodium monosulphide and sulphur, rather than sodium polysulphide, the latter then forming in situ. In examples: (1) a mixture of carbon dioxide and ethylene oxide is passed into an aqueous solution of sodium sulphide and sulphur yielding bis-(hydroxyethyl) polysulphide of a sulphur content of 33 or 42.8 per cent depending on the sulphur content of the initial reaction mixture; (2) ethylene oxide is passed into an aqueous solution of sodium sulphide and sulphur while sulphuric acid is added dropwise with agitation; a bis-(hydroxyethyl) polysulphide is obtained and this product and the second product of (1) are catalytically hydrogenated to thioglycol.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE733947X | 1952-03-22 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB733947A true GB733947A (en) | 1955-07-20 |
Family
ID=6641196
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB7686/53A Expired GB733947A (en) | 1952-03-22 | 1953-03-19 | Manufacture of bis-(ª‰-hydroxyalkyl-) polysulphides |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB733947A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN112358497A (en) * | 2020-11-19 | 2021-02-12 | 南京曙光精细化工有限公司 | Preparation method of polysulfide silane coupling agent with lighter color |
-
1953
- 1953-03-19 GB GB7686/53A patent/GB733947A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN112358497A (en) * | 2020-11-19 | 2021-02-12 | 南京曙光精细化工有限公司 | Preparation method of polysulfide silane coupling agent with lighter color |
CN112358497B (en) * | 2020-11-19 | 2023-08-25 | 南京曙光新材料有限公司 | Preparation method of polysulfide silane coupling agent with lighter color |
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