http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2007014309-A3
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_04bfe084ec43447bb282b2730641d1ab http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_ff3f9ec831c7ba90ea2ae344975e5faa http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_1a691474573861b8f94a2726e16b8239 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G73-16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G69-44 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G63-685 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D209-48 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G63-16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G69-26 |
| filingDate | 2006-07-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ad515a6276074fa8fcfab32e0a4e4de8 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6c0c19eda70cddfbe2a9b8bf503f32e3 |
| publicationDate | 2007-08-16-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | WO-2007014309-A3 |
| titleOfInvention | N-hydroxyalkyltrimellitimide esters and bis-(trimellitimide) esters and method of making |
| abstract | The present invention relates to trimellitic anhydride imide ester, a method of making it, and polyesters or polyamides that can be modified with trimellitic anhydride (TMA) to provide better heat resistance and mechanical properties. With the present invention, there are two processes for making TMA-ester. The first process is by charging into a reactor equimolar amounts of trimellitic anhydride and primary hydroxyalkylamine, primary carboxylalkylamine or primary carboxylarylamine, with an excess of alcohol or diol. The second process for producing the imide ester is to react two moles of TMA with one mole of a diamine of the formula H2N-X-NH2 with an excess of alcohol or diol; where X is an aliphatic, alicyclic, or aromatic group. Generally the reactor contains water as a dispersant for the reactants. The reaction time is from about 1 - 8 hours. The reaction temperature is from about 160° C to about 220° C. After the cessation of water/alcohol production, the reaction is finished and the contents of the reactor can be cooled to cause the desired solid product to precipitate our. The solid is then separated by filtration or centrifugation. |
| priorityDate | 2005-07-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 36.