http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-1313072-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G69-48
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G59-58
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/D06M15-37
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/D06M15-55
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G59-58
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/D06M15-37
filingDate 1971-06-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_41a43f0d6c10a34ba14e117208180aed
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_11c444a3529d08c2cc96fa727f34bf5b
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publicationDate 1973-04-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-1313072-A
titleOfInvention Preparations of reactions products of epoxides fatty amines and dicarboxylic acids processes for their manufacture and their use
abstract 1313072 Antifelting treatment for wool; sizing paper CIBA-GEIGY AG 8 June 1971 [9 June 1970 22 Jan 1971] 19450/71 Headings D1P and D2B [Also in Division C3] Wool is rendered non felting and paper may be sized by treatment with a composition comprising a polyepoxide (I) containing at least two epoxy groups per molecule, a C 12-24 fattyamine (II) and an aliphatic saturated dicarboxylic acid (III) containing at least 7 carbon atoms reacted together to form a stable preparation which by adding (if necessary) ammonia or water soluble organic base has a pH value of 7.5-12 on dilution with water. The following optional ingredients may also be present in the reaction mixture: an anhydride of an aromatic dicarboxylic acid (at least C 8 ) or of an aliphatic mono- or di-carboxylic acid (at least C 4 ), an aminoplast precondensate containing alkylether groups, a C 2-22 aliphatic diol, another polyfunctional compound containing labile halogen, vinyl or ester groups together with at most one acid, nitrile OH or epoxy group. The starting materials are reacted together, e.g. at 80-120‹C in an organic solvent, e.g. ethylene glycol monobutyl ether. I may be a diglycidyl ether of bisphenol A. II may have the formula Me(CH 2 ) x NH 2 in which x = 11-23. III may have the formula HOOC(CH 2 ) v COOH in which y = 5-12. The wool may be pretreated with dichloroisocyanuric acid or a salt thereof. In an example wool yarn is first dyed with a reactive dye in a circulation bath and rinsed. It was then placed in a water containing 41. water and warmed to 40‹C, then 1 Kg. oxalic acid and 0.2 Kg. of a condensate of 1 mol of a C 16-20 fatty amine and 70 mol ethylene oxide was introduced followed by 10 Kg of a product according to the invention. An emulsion formed which was uniformly absorbed on the wool in 20-30 minutes and thereafter the condensation product of tristearoyl ethylene triamine and ethylene oxide was added as softener. The product may be steamed. The treating bath may optionally contain anonyl phenol ethylene oxide condensate, diammonium phosphate and monoethanolamine sulphite.
priorityDate 1970-06-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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