http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-1059159-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_5c24684033fba97d1ad845ce453a57e3 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08K5-3475 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08K5-13 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08K5-372 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08K5-13 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08K5-372 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08K5-3475 |
| filingDate | 1965-04-14-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 1967-02-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | GB-1059159-A |
| titleOfInvention | Stabilized polyalkylene oxides and process for preparing them |
| abstract | Polyalkylene oxides are stabilized by a mixture of the following compounds:-(I) a compound of formula <FORM:1059159/C3/1> and (II) a compound of formula <FORM:1059159/C3/2> and (III) a compound of formula R4-Sn-R5, wherein R is a hydrogen or halogen atom or an alkyl or alkoxy group, R1 is hydrogen or an alkyl radical, A is S or CH2, R2 and R3 are each an alkyl radical of 1 to 4 carbon atoms, n is 1 to 4, R4 and R5 are each an alkyl radical or a (CH2)m.COOR8 group, wherein R6 is an alkyl radical and m is 1 to 4. Suitable polyalkylene oxides are those obtained by polymerizing saturated alkylene oxides, halo-substituted opoxides, including epichlorohydrin, cycloalphatic epoxides, or epoxy ethers, including glycidyl ethers, or by copolymerizing saturated epoxides with unsaturated epoxides, e.g. glycidyl acrylate. Typical examples of compound (I) are 2(21-hydroxy-phenyl-) benzotriazole, 2(21 - hydroxy - 31 - methyl - 51 - t. - butyl phenyl-) benzotriazole, 2(21-hydroxy-31,51-di methylphenyl) - 5 - methoxybenzotriazole, and 2(21 - hydroxy - 31,51 - di - t. - butyl - phenyl-)5-chloro-benzotriazole. Typical examples of compound (II) are bis(4-hydroxy-2-propyl-5-t.-butyl)methane and bis(4 - hydroxy - 2,5 - di-t.-butylphenyl)sulphide. Examples of compound (III) are di(dodecyl) sulphide, di(octadecyl)-trisulphide, thiodipropionic acid octadecyl ester, and tetrasulphide (diacetic acid octadecyl ester). The stabilizer may be added as a solid or in solution. The stabilized polymers may be cross-linked, and may also be caused to swell or dissolved by, e.g., dimethyl formamide, tetramethylene sulphone, dioxane, methanol, benzene, and chlorinated hydrocarbons. Soots, fillers, dyes or pigments, extender oils or lubricants may also be added. The example describes the stabilization of a methanolic solution of a propylene oxide-allyl glycidyl ether copolymer, thiourea, silicic acid, zinc oxide, dipentamethylene thiuram tetrasulphide, 2-mercaptobenzothiazole and titanium dioxide composition with a mixture of 0.5% by weight of bis(4 - hydroxy - 5 - t. - butyl - 2 - methylphenyl) sulphide, 0.5% by weight of di(octadecyl) disulphide, 2% by weight of, in one case, 2[21 - hydroxy - 31,51 - di(t. - butyl)phenyl]-5-chlorobenzotriazole, and, in a second run, 2[21 - hydroxy - 51 - methyl - phenyl]benzotriazole, the percentage being based on the weight of copolymer composition. The resulting polymer was spun and the filaments cross-linked. |
| priorityDate | 1964-04-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
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Total number of triples: 62.