Verfahren zur Herstellung von Mischpolymerisaten fuer die Herstellung elastischer Faeden und Fasern
A substantially linear polyester-urethaneurea is prepared by (a) heating a difunctional hydroxy-terminated polyester with a molar insufficiency of an aromatic diisocyanate, (b) heating the product hydroxy-terminated polyester-urethane with an aliphatic diisocyanate, and (c) mixing the isocyanate-ter...
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description | A substantially linear polyester-urethaneurea is prepared by (a) heating a difunctional hydroxy-terminated polyester with a molar insufficiency of an aromatic diisocyanate, (b) heating the product hydroxy-terminated polyester-urethane with an aliphatic diisocyanate, and (c) mixing the isocyanate-terminated product with p-menthane-1:8-diamine. Suitable polyesters may have M.W. between 1500 and 2500, and may be derived from e.g. malonic, succinic, terephthalic, adipic, methyladipic, maleic, sebacic and suberic acids and ethylene, propylene, trimethylene, 1:3-butylene, tetramethylene, hexamethylene, diethylene, neopentyl and decamethylene glycols. Suitable diisocyanates are 4:41-diphenylmethane-, 4:41-bis(3-methylphenyl)methane-, toluylene and m-phenylene diisocyanates and tetramethylene-, hexamethylene-, 4:41-bis(cyclohexylene)methane-, 1:4-cyclohexylene- and 1:4-dimethylene-cyclohexane - diisocyanates. Reaction (b) is preferably conducted i.p.o. an organo-tin catalyst, and reaction (c) preferably in an inert solvent, e.g. dimethylformamide, dimethylacetamide, dimethylpropionamide, dimethylsulphoxide and tetramethylurea. In examples a polyethylene adipate or polyethylene-propylene adipate diol is reacted with 4:41-methylene-bis(phenylisocyanate) and then with 4:41 - methylene - bis(cyclohexane isocyanate) and finally with p-menthane-1:8-diamine in dimethylformamide, the products being extruded into hot water to give elastic fibres. |
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Suitable polyesters may have M.W. between 1500 and 2500, and may be derived from e.g. malonic, succinic, terephthalic, adipic, methyladipic, maleic, sebacic and suberic acids and ethylene, propylene, trimethylene, 1:3-butylene, tetramethylene, hexamethylene, diethylene, neopentyl and decamethylene glycols. Suitable diisocyanates are 4:41-diphenylmethane-, 4:41-bis(3-methylphenyl)methane-, toluylene and m-phenylene diisocyanates and tetramethylene-, hexamethylene-, 4:41-bis(cyclohexylene)methane-, 1:4-cyclohexylene- and 1:4-dimethylene-cyclohexane - diisocyanates. Reaction (b) is preferably conducted i.p.o. an organo-tin catalyst, and reaction (c) preferably in an inert solvent, e.g. dimethylformamide, dimethylacetamide, dimethylpropionamide, dimethylsulphoxide and tetramethylurea. In examples a polyethylene adipate or polyethylene-propylene adipate diol is reacted with 4:41-methylene-bis(phenylisocyanate) and then with 4:41 - methylene - bis(cyclohexane isocyanate) and finally with p-menthane-1:8-diamine in dimethylformamide, the products being extruded into hot water to give elastic fibres.</description><language>ger</language><subject>CHEMISTRY ; COMPOSITIONS BASED THEREON ; MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONSONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS ; METALLURGY ; ORGANIC MACROMOLECULAR COMPOUNDS ; THEIR PREPARATION OR CHEMICAL WORKING-UP</subject><creationdate>1969</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19690828&DB=EPODOC&CC=DE&NR=1570227A1$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,777,882,25545,76296</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19690828&DB=EPODOC&CC=DE&NR=1570227A1$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>TAUB,BERNARD</creatorcontrib><title>Verfahren zur Herstellung von Mischpolymerisaten fuer die Herstellung elastischer Faeden und Fasern</title><description>A substantially linear polyester-urethaneurea is prepared by (a) heating a difunctional hydroxy-terminated polyester with a molar insufficiency of an aromatic diisocyanate, (b) heating the product hydroxy-terminated polyester-urethane with an aliphatic diisocyanate, and (c) mixing the isocyanate-terminated product with p-menthane-1:8-diamine. Suitable polyesters may have M.W. between 1500 and 2500, and may be derived from e.g. malonic, succinic, terephthalic, adipic, methyladipic, maleic, sebacic and suberic acids and ethylene, propylene, trimethylene, 1:3-butylene, tetramethylene, hexamethylene, diethylene, neopentyl and decamethylene glycols. Suitable diisocyanates are 4:41-diphenylmethane-, 4:41-bis(3-methylphenyl)methane-, toluylene and m-phenylene diisocyanates and tetramethylene-, hexamethylene-, 4:41-bis(cyclohexylene)methane-, 1:4-cyclohexylene- and 1:4-dimethylene-cyclohexane - diisocyanates. Reaction (b) is preferably conducted i.p.o. an organo-tin catalyst, and reaction (c) preferably in an inert solvent, e.g. dimethylformamide, dimethylacetamide, dimethylpropionamide, dimethylsulphoxide and tetramethylurea. In examples a polyethylene adipate or polyethylene-propylene adipate diol is reacted with 4:41-methylene-bis(phenylisocyanate) and then with 4:41 - methylene - bis(cyclohexane isocyanate) and finally with p-menthane-1:8-diamine in dimethylformamide, the products being extruded into hot water to give elastic fibres.</description><subject>CHEMISTRY</subject><subject>COMPOSITIONS BASED THEREON</subject><subject>MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONSONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS</subject><subject>METALLURGY</subject><subject>ORGANIC MACROMOLECULAR COMPOUNDS</subject><subject>THEIR PREPARATION OR CHEMICAL WORKING-UP</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1969</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNqNyrEKwjAUheEuDqK-Q15AsBXpLLWli5u4lpCc2EBMwr2JoE9vBBc3p_PD-ZaVuoKMnAlevDKJEcQJzmV_E4_gxdmymmNwzzvIskyFmQwS2uLHwklOH1u-QUIXl70uySC_rhZGOsbmu6tKDP2lG7eIYQJHqeCRplNfH9pd07THev8HeQN7Uj59</recordid><startdate>19690828</startdate><enddate>19690828</enddate><creator>TAUB,BERNARD</creator><scope>EVB</scope></search><sort><creationdate>19690828</creationdate><title>Verfahren zur Herstellung von Mischpolymerisaten fuer die Herstellung elastischer Faeden und Fasern</title><author>TAUB,BERNARD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_DE1570227A13</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>ger</language><creationdate>1969</creationdate><topic>CHEMISTRY</topic><topic>COMPOSITIONS BASED THEREON</topic><topic>MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONSONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS</topic><topic>METALLURGY</topic><topic>ORGANIC MACROMOLECULAR COMPOUNDS</topic><topic>THEIR PREPARATION OR CHEMICAL WORKING-UP</topic><toplevel>online_resources</toplevel><creatorcontrib>TAUB,BERNARD</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>TAUB,BERNARD</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Verfahren zur Herstellung von Mischpolymerisaten fuer die Herstellung elastischer Faeden und Fasern</title><date>1969-08-28</date><risdate>1969</risdate><abstract>A substantially linear polyester-urethaneurea is prepared by (a) heating a difunctional hydroxy-terminated polyester with a molar insufficiency of an aromatic diisocyanate, (b) heating the product hydroxy-terminated polyester-urethane with an aliphatic diisocyanate, and (c) mixing the isocyanate-terminated product with p-menthane-1:8-diamine. Suitable polyesters may have M.W. between 1500 and 2500, and may be derived from e.g. malonic, succinic, terephthalic, adipic, methyladipic, maleic, sebacic and suberic acids and ethylene, propylene, trimethylene, 1:3-butylene, tetramethylene, hexamethylene, diethylene, neopentyl and decamethylene glycols. Suitable diisocyanates are 4:41-diphenylmethane-, 4:41-bis(3-methylphenyl)methane-, toluylene and m-phenylene diisocyanates and tetramethylene-, hexamethylene-, 4:41-bis(cyclohexylene)methane-, 1:4-cyclohexylene- and 1:4-dimethylene-cyclohexane - diisocyanates. Reaction (b) is preferably conducted i.p.o. an organo-tin catalyst, and reaction (c) preferably in an inert solvent, e.g. dimethylformamide, dimethylacetamide, dimethylpropionamide, dimethylsulphoxide and tetramethylurea. In examples a polyethylene adipate or polyethylene-propylene adipate diol is reacted with 4:41-methylene-bis(phenylisocyanate) and then with 4:41 - methylene - bis(cyclohexane isocyanate) and finally with p-menthane-1:8-diamine in dimethylformamide, the products being extruded into hot water to give elastic fibres.</abstract><oa>free_for_read</oa></addata></record> |
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subjects | CHEMISTRY COMPOSITIONS BASED THEREON MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONSONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS METALLURGY ORGANIC MACROMOLECULAR COMPOUNDS THEIR PREPARATION OR CHEMICAL WORKING-UP |
title | Verfahren zur Herstellung von Mischpolymerisaten fuer die Herstellung elastischer Faeden und Fasern |
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