http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-859639-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_9e5302e08e56037ff7bc5c9b6fcc29f9 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G63-823 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G63-82 |
| filingDate | 1957-04-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 1961-01-25-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | GB-859639-A |
| titleOfInvention | Process for preparing polyesters from lactones |
| abstract | In the manufacture of a polyester by reacting a lactone having at least six carbon atoms in the ring with an organic compound containing at least one alcholic hydroxyl or a primary or secondary amino group attached directly to carbon, the reaction is effected in presence of 0,001- 1% of a catalyst which is an organo tin compound or a lead or manganese salt of an organic carboxylic acid. The lactones and the initiators (which may be monomeric or polymeric) are as specified in Specification 859,642. The organo tin compound preferably has the formula: <FORM:0859639/IV(a)/1> and <FORM:0859639/IV(a)/2> where X is an alkyl, aryl, aralkyl or aryloxy radical and X1 is in alkyl aryl, aralkyl, acyloxy, halogen or hydroxyl radical. For example tetraphenyl tin, tetraoctyl tin, diphenyl tin dilaurate, tri-n-butyltin hydroxide, tri-n-butyltin acetate, dimethyltin oxide, di-n-butyltin dichloride and diocytltin dichloride. Specified lead and manganese salts are lead acetate, manganese acetate, lead 2-ethylhexoate and lead benzoate. Polymerization of the lactone is preferably effected at 50 DEG -300 DEG C. in the absence of oxygen until the refractive index of the polyester becomes constant and at the end of the reaction unreacted monomer may be removed by applying a vacuum. The polyesters generally have a molecular weight of 500-12,000. They may be used as plasticizers, e.g. for vinyl chloride-vinyl acetate resins, especially if the terminal hydroxyl groups are acylated or may be reacted with isocyanates to form polyurethanes. Examples describe the polymerization of epsilon-caprolactone, alkyl, dialkyl and trialkyl caprolactones, zeta-enantholactone and various mixtures thereof. Specifications 859,640, 859,641, 859,643, 859,644 and 859,645 also are referred to. |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5225129-A |
| priorityDate | 1956-04-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 49.