http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-280990-A
Outgoing Links
Predicate | Object |
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assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_6108c9a7f7a472c2db8923daca0ec8d6 http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_e2a4d0883f4b8a98add27915d433eda4 |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/D06M13-07 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/D06M13-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/D06M13-144 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/D06M13-188 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/D06M13-07 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/D06M13-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/D06M13-144 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/D06M13-188 |
filingDate | 1926-07-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationDate | 1927-11-28-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | GB-280990-A |
titleOfInvention | Improvements in or relating to the treatment of fabrics |
abstract | 280,990. British Gelanese, Ltd., and Ellis, G. H. July 27, 1926. Yarns and threads, treating with liquids.-Fabrics made of or containing cellulose ethers or esters are treated without loading to increase the friction between the fibres, e.g. to reduce laddering with one or more organic substances having a solvent or solute action upon the fibres or with solutions or dispersions of such substances of at least 5 per cent. concentration by weight. Examples of such organic solvents or solutes are as follows :- (a) Hydrocarbons such as those, of the paraffin, aromatic, naphthene or terpene series, and their hydrogenated and halogenated derivatives for examples; hexane, decane, dodecane, or higher paraffin hydrocarbons or mixtures of such as may occur in various commercial liquid paraffins like gasoline. and the like. benzene, toluene, xylenes, naphthalenes, dekanaphthene, undekanaphthene, dodekanaphthene, pinene, sylvestrene, hexahydrobenzene, tetrahydronaphthalene, trichlorethylene, tetrachlorethane, chlor or polychlor benzenes, chlor or polychlor toluenes, chlor or polychlor xylenes, alphachlornaphthalene, betachlornaphthalene, poly chlornaphthalenes; (b) alcoholic and phenolic bodies of the various chemical series, and their halogenated or hydrogenated derivatives, for instance, ethyl alcohol, propylalcohol, glycerol, phenol cresols, xylenols, hexahydrophenol, alphanaphthol, betanaphthol, resorcin, catechol, guaiacol, anisol, tetrahydro naphthol, chlorhydrin, chlorphenol, chlornaphthols; (c) Amino compounds, or their hydroxy or halogenated derivatives, for instance, aniline, alkyl- or diatkylanilines, alkyl or dialkyl toluidines, alkyl or dialkyl xylidines, benzylaniline, diphenylamine, naphthylamines, alkyl and aryl naphthylamines such as phenyl- and ethylalphanaphthylamines, chloranilines, chlornaphthylamines, aminophenols, aminonaphthols, alkylaminophenols, alkylaminonaphthols; (d) Ketonic, aldehydic substances such as acetone, diacetonealcohol, formaldehyde, benzaldehyde, and miscellaneous organic substances for example nitro derivatives such as nitrobenzene, nitrotoluene, and the like; (3 Carbocyclic sulphonic or carboxylic acids, such as those of the benzene, naphthalene or anthracene series, or derivatives thereof such as phenolsulphonic acids, or sodium, ammonium or other alkali salts of such acids. These reagents may be applied as such, in solution in ordinary solvents, or in colloidal dispersion in aqueous media. These colloidal dispersions may be formed by the methods described in Specifications 219,349, 224,925, 242,393, 273,819, or 273,820, [all in Class 15 (ii), Dyeing, Processes &c. for]. Specifications 165,164 and 206,818, [both in Class 15 (ii), Dyeing, Processes &c. for], also are referred to. |
isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-3016280-A |
priorityDate | 1926-07-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 114.