DE1024049B - Verfahren zum Knitterfest- und Schrumpffestmachen von Textilien - Google Patents
Verfahren zum Knitterfest- und Schrumpffestmachen von TextilienInfo
- Publication number
- DE1024049B DE1024049B DEN6423A DEN0006423A DE1024049B DE 1024049 B DE1024049 B DE 1024049B DE N6423 A DEN6423 A DE N6423A DE N0006423 A DEN0006423 A DE N0006423A DE 1024049 B DE1024049 B DE 1024049B
- Authority
- DE
- Germany
- Prior art keywords
- proof
- ethoxylin
- parts
- epoxy
- condensate
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000004753 textile Substances 0.000 title claims description 31
- 238000000034 method Methods 0.000 title claims description 12
- 150000001875 compounds Chemical class 0.000 claims description 29
- 239000004593 Epoxy Substances 0.000 claims description 18
- 125000003700 epoxy group Chemical group 0.000 claims description 18
- 239000003795 chemical substances by application Substances 0.000 claims description 14
- 229920005989 resin Polymers 0.000 claims description 11
- 239000011347 resin Substances 0.000 claims description 11
- 239000000463 material Substances 0.000 claims description 9
- STMDPCBYJCIZOD-UHFFFAOYSA-N 2-(2,4-dinitroanilino)-4-methylpentanoic acid Chemical compound CC(C)CC(C(O)=O)NC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O STMDPCBYJCIZOD-UHFFFAOYSA-N 0.000 claims description 6
- -1 epoxy groups Compound Chemical class 0.000 claims description 6
- IWDCLRJOBJJRNH-UHFFFAOYSA-N p-cresol Chemical compound CC1=CC=C(O)C=C1 IWDCLRJOBJJRNH-UHFFFAOYSA-N 0.000 claims description 6
- 239000000835 fiber Substances 0.000 claims description 5
- 229920000642 polymer Polymers 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 150000005846 sugar alcohols Polymers 0.000 claims description 4
- 230000002378 acidificating effect Effects 0.000 claims description 3
- 150000001735 carboxylic acids Chemical class 0.000 claims description 3
- 150000002989 phenols Chemical class 0.000 claims description 3
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 2
- 229910052796 boron Inorganic materials 0.000 claims description 2
- 238000000576 coating method Methods 0.000 claims description 2
- 150000008065 acid anhydrides Chemical class 0.000 claims 1
- 239000011248 coating agent Substances 0.000 claims 1
- 239000004033 plastic Substances 0.000 claims 1
- 229920003023 plastic Polymers 0.000 claims 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 30
- 239000004744 fabric Substances 0.000 description 20
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 18
- 239000000243 solution Substances 0.000 description 17
- 239000007788 liquid Substances 0.000 description 15
- 239000000203 mixture Substances 0.000 description 14
- 238000011084 recovery Methods 0.000 description 8
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 7
- 239000000460 chlorine Substances 0.000 description 7
- 229910052801 chlorine Inorganic materials 0.000 description 7
- 229920000742 Cotton Polymers 0.000 description 6
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 6
- 229920001807 Urea-formaldehyde Polymers 0.000 description 6
- 238000005470 impregnation Methods 0.000 description 6
- GZCGUPFRVQAUEE-SLPGGIOYSA-N aldehydo-D-glucose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O GZCGUPFRVQAUEE-SLPGGIOYSA-N 0.000 description 5
- 239000003995 emulsifying agent Substances 0.000 description 5
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 4
- 239000000839 emulsion Substances 0.000 description 4
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 229920000877 Melamine resin Polymers 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical class FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 3
- 229910052742 iron Inorganic materials 0.000 description 3
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 3
- 239000004014 plasticizer Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 229920000297 Rayon Polymers 0.000 description 2
- 150000008064 anhydrides Chemical class 0.000 description 2
- 239000004202 carbamide Substances 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 239000003431 cross linking reagent Substances 0.000 description 2
- 238000002845 discoloration Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- WQYVRQLZKVEZGA-UHFFFAOYSA-N hypochlorite Chemical compound Cl[O-] WQYVRQLZKVEZGA-UHFFFAOYSA-N 0.000 description 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- 239000004848 polyfunctional curative Substances 0.000 description 2
- 239000001294 propane Substances 0.000 description 2
- 239000002964 rayon Substances 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 2
- 230000004580 weight loss Effects 0.000 description 2
- 210000002268 wool Anatomy 0.000 description 2
- 230000037303 wrinkles Effects 0.000 description 2
- 239000001124 (E)-prop-1-ene-1,2,3-tricarboxylic acid Substances 0.000 description 1
- ZORQXIQZAOLNGE-UHFFFAOYSA-N 1,1-difluorocyclohexane Chemical compound FC1(F)CCCCC1 ZORQXIQZAOLNGE-UHFFFAOYSA-N 0.000 description 1
- IPDWABJNXLNLRA-UHFFFAOYSA-N 2,3-dihydroxybutanedioic acid;2-hydroxypropane-1,2,3-tricarboxylic acid Chemical compound OC(=O)C(O)C(O)C(O)=O.OC(=O)CC(O)(C(O)=O)CC(O)=O IPDWABJNXLNLRA-UHFFFAOYSA-N 0.000 description 1
- WISUILQECWFZCN-UHFFFAOYSA-N 2-(oxiran-2-ylmethylsulfanylmethyl)oxirane Chemical compound C1OC1CSCC1CO1 WISUILQECWFZCN-UHFFFAOYSA-N 0.000 description 1
- HOSGXJWQVBHGLT-UHFFFAOYSA-N 6-hydroxy-3,4-dihydro-1h-quinolin-2-one Chemical group N1C(=O)CCC2=CC(O)=CC=C21 HOSGXJWQVBHGLT-UHFFFAOYSA-N 0.000 description 1
- 229920002955 Art silk Polymers 0.000 description 1
- 229910015900 BF3 Inorganic materials 0.000 description 1
- 241000792859 Enema Species 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- 241000322338 Loeseliastrum Species 0.000 description 1
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 150000001241 acetals Chemical class 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 229940091181 aconitic acid Drugs 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 230000001153 anti-wrinkle effect Effects 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 238000004061 bleaching Methods 0.000 description 1
- 239000007844 bleaching agent Substances 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- GTZCVFVGUGFEME-IWQZZHSRSA-N cis-aconitic acid Chemical compound OC(=O)C\C(C(O)=O)=C\C(O)=O GTZCVFVGUGFEME-IWQZZHSRSA-N 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- LSXWFXONGKSEMY-UHFFFAOYSA-N di-tert-butyl peroxide Chemical compound CC(C)(C)OOC(C)(C)C LSXWFXONGKSEMY-UHFFFAOYSA-N 0.000 description 1
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical class C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000007920 enema Substances 0.000 description 1
- 229940095399 enema Drugs 0.000 description 1
- LJCCYDSSNYGHJH-UHFFFAOYSA-N ethane-1,2-diol;propane Chemical compound CCC.OCCO LJCCYDSSNYGHJH-UHFFFAOYSA-N 0.000 description 1
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 238000010409 ironing Methods 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- RCHKEJKUUXXBSM-UHFFFAOYSA-N n-benzyl-2-(3-formylindol-1-yl)acetamide Chemical compound C12=CC=CC=C2C(C=O)=CN1CC(=O)NCC1=CC=CC=C1 RCHKEJKUUXXBSM-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 150000004968 peroxymonosulfuric acids Chemical class 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- ODGAOXROABLFNM-UHFFFAOYSA-N polynoxylin Chemical compound O=C.NC(N)=O ODGAOXROABLFNM-UHFFFAOYSA-N 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 235000011069 sorbitan monooleate Nutrition 0.000 description 1
- 239000001593 sorbitan monooleate Substances 0.000 description 1
- 229940035049 sorbitan monooleate Drugs 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- GTZCVFVGUGFEME-UHFFFAOYSA-N trans-aconitic acid Natural products OC(=O)CC(C(O)=O)=CC(O)=O GTZCVFVGUGFEME-UHFFFAOYSA-N 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
- C08G59/62—Alcohols or phenols
- C08G59/625—Hydroxyacids
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/55—Epoxy resins
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S8/00—Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
- Y10S8/08—Oxirane
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US259504A US2752269A (en) | 1951-12-01 | 1951-12-01 | Treatment of textile materials |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1024049B true DE1024049B (de) | 1958-02-13 |
Family
ID=22985230
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DEN6423A Pending DE1024049B (de) | 1951-12-01 | 1952-11-29 | Verfahren zum Knitterfest- und Schrumpffestmachen von Textilien |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US2752269A (enrdf_load_stackoverflow) |
| BE (1) | BE515900A (enrdf_load_stackoverflow) |
| DE (1) | DE1024049B (enrdf_load_stackoverflow) |
| FR (1) | FR1071905A (enrdf_load_stackoverflow) |
| GB (1) | GB732573A (enrdf_load_stackoverflow) |
| NL (1) | NL174182B (enrdf_load_stackoverflow) |
Families Citing this family (52)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3073662A (en) * | 1963-01-15 | Process for the production of fast dye- | ||
| US2903381A (en) * | 1954-09-03 | 1959-09-08 | Shell Dev | Treatment of synthetic textiles with a polyepoxide having a plurality of 1,2 epoxy groups |
| US2829071A (en) * | 1954-04-26 | 1958-04-01 | Shell Dev | Treatment of wool containing textiles |
| US2829072A (en) * | 1954-05-19 | 1958-04-01 | Bates Mfg Co | Process for the treatment of textile materials with epoxy resins and for curing the same |
| BE541693A (enrdf_load_stackoverflow) * | 1954-10-04 | 1900-01-01 | ||
| US2841595A (en) * | 1955-01-31 | 1958-07-01 | Shell Dev | Process for manufacture of glycidyl ethers of polyhydric phenols |
| GB796815A (en) * | 1955-02-22 | 1958-06-18 | Courtaulds Inc | Improvements in and relating to the production of an aminoplast precondensate for the treatment of cellulosic textile materials |
| BE546441A (enrdf_load_stackoverflow) * | 1955-03-28 | |||
| NL109055C (enrdf_load_stackoverflow) * | 1955-06-28 | |||
| US2826514A (en) * | 1955-11-17 | 1958-03-11 | Shell Dev | Treatment of textile materials and composition therefor |
| GB853619A (en) * | 1956-02-06 | 1960-11-09 | Rohm & Haas | New unsaturated glycidyl ethers, polymers thereof and methods for producing them |
| US2886472A (en) * | 1956-04-27 | 1959-05-12 | Shell Dev | Treatment of textile materials |
| US2794754A (en) * | 1956-04-30 | 1957-06-04 | Shell Dev | Treatment of textile materials |
| NL221263A (enrdf_load_stackoverflow) * | 1956-10-05 | |||
| US2928794A (en) * | 1956-12-05 | 1960-03-15 | Devoe & Raynolds Co Inc | Curing of polyepoxides |
| US2928808A (en) * | 1956-12-10 | 1960-03-15 | Devoe & Raynolds Co Inc | Curing of polyepoxides |
| US2869970A (en) * | 1957-04-11 | 1959-01-20 | Edward M Filachione | Tanning with epoxy resins |
| US3024080A (en) * | 1957-10-14 | 1962-03-06 | Rohm & Haas | 2, 6-dioxaspiro (3, 3)heptane treated cellulose fabric and the production thereof |
| DE1155666B (de) * | 1957-11-02 | 1963-10-10 | Schickedanz Ver Papierwerk | Verfahren zur Herstellung von saugfaehigen und wasserbestaendigen Flaechengebilden aus Cellulosefasern |
| US2928810A (en) * | 1957-11-15 | 1960-03-15 | Devoe & Raynolds Co | Aliphatic alcohol-epoxide resin compositions |
| US2928811A (en) * | 1957-11-18 | 1960-03-15 | Devoe & Raynolds Co | Epoxide resin-amide compositions |
| US3036041A (en) * | 1957-12-23 | 1962-05-22 | Richardson Co | Reaction products of epoxylated compositions and process |
| US3073799A (en) * | 1958-01-20 | 1963-01-15 | Gen Electric | Resin compositions and their preparation |
| NL240376A (enrdf_load_stackoverflow) * | 1958-06-19 | |||
| US3019076A (en) * | 1958-07-22 | 1962-01-30 | Jr Clay E Pardo | Treatment of textiles with polyepoxides and polyamides |
| US3043813A (en) * | 1958-10-03 | 1962-07-10 | Union Carbide Corp | Polymer of alkenyl epoxycyclopentyl ethers |
| US3026216A (en) * | 1959-10-05 | 1962-03-20 | Union Carbide Corp | Treatment of textile fabrics with methylglycidyl ethers |
| US3128147A (en) * | 1959-09-30 | 1964-04-07 | Courtaulds Ltd | Process for treating polynosic fibers and products obtained thereby |
| US3084073A (en) * | 1959-12-10 | 1963-04-02 | Rohm & Haas | Copolymers of alkyl acrylate, methoxymethyl vinyl sulfide, comonomer containing functional groups, and coating compositions thereof |
| US3097050A (en) * | 1959-12-28 | 1963-07-09 | Rohm & Haas | Process of creaseproofing cellulose fabrics with 2, 6-dioxaspiro (3, 3) heaptane and ormaldehyde and fabrics produced thereby |
| US3150190A (en) * | 1960-02-18 | 1964-09-22 | Quaker Chem Corp | Acetal condensation products and their preparation |
| NL261845A (enrdf_load_stackoverflow) * | 1960-03-01 | 1900-01-01 | ||
| US3131083A (en) * | 1960-03-25 | 1964-04-28 | Standard Packaging Corp | Method of impregnating card stock |
| US3228920A (en) * | 1960-05-12 | 1966-01-11 | Metal Recovery Systems | Chelating resins and method of preparation |
| US3069311A (en) * | 1962-03-28 | 1962-12-18 | Hercules Powder Co Ltd | Paper manufacture |
| US3321099A (en) * | 1963-02-04 | 1967-05-23 | Dow Chemical Co | Composition for the lamination of glass by means of epoxy resinous materials |
| US3382030A (en) * | 1963-11-08 | 1968-05-07 | Agriculture Usa | Modification of cellulose with butadiene diepoxide using a dioxane-water solvent system |
| US3377406A (en) * | 1963-12-16 | 1968-04-09 | Shell Oil Co | Process of esterification of polyepoxides with ethylenically unsaturated monocarboxylic acids in the presence of onium salts of inorganic acids |
| DE1300695B (de) * | 1963-12-21 | 1969-08-07 | Henkel & Cie Gmbh | Verfahren zur Herstellung von Formkoerpern, UEberzuegen und Verklebungen auf der Basis von Epoxydpolyaddukten |
| US3293073A (en) * | 1964-02-12 | 1966-12-20 | Union Carbide Corp | Process for imparting wash and wear properties to cellulose-containing textile fabric and resulting product |
| US3293071A (en) * | 1964-02-14 | 1966-12-20 | Union Carbide Corp | Process for treating cellulosic textile material |
| US3313796A (en) * | 1964-02-24 | 1967-04-11 | Monsanto Co | Process for improving the antistatic properties of synthetic articles |
| NL131186C (enrdf_load_stackoverflow) * | 1964-12-24 | 1900-01-01 | ||
| CH1795665D (enrdf_load_stackoverflow) * | 1964-12-30 | |||
| US3408184A (en) * | 1965-01-18 | 1968-10-29 | Xerox Corp | Electrophotographic materials and methods employing photoconductive resinous charge transfers complexes |
| US3408182A (en) * | 1965-01-18 | 1968-10-29 | Xerox Corp | Electrophotographic materials and methods employing photoconductive resinous charge transfer complexes |
| US3402988A (en) * | 1965-04-02 | 1968-09-24 | Agriculture Usa | Chemical deactivation of catalyst at both faces of a cellulosic fabric impregnated with a resin-catalyst system to improve abrasion resistance of fabric after curing |
| GB1174344A (en) * | 1967-02-13 | 1969-12-17 | Ciba Ltd | Epoxide-Containing Compositions |
| US4240971A (en) * | 1969-07-18 | 1980-12-23 | Hercules Incorporated | Epoxy-sulfonylazide compounds |
| US4049851A (en) * | 1975-03-21 | 1977-09-20 | Basf Aktiengesellschaft | Manufacture of bonded textile sheet materials |
| EP1138819B1 (en) * | 2000-03-31 | 2007-09-12 | Kao Corporation | Fiber product treating agents |
| JP5646572B2 (ja) * | 2012-10-16 | 2014-12-24 | 日本蚕毛染色株式会社 | 改質繊維およびその製造方法 |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2455083A (en) * | 1945-05-08 | 1948-11-30 | Pacific Mills | Cellulose ethers of 3, 4 epoxy 1-butene and their oxidation products |
| US2464753A (en) * | 1947-03-25 | 1949-03-15 | Shell Dev | Allyl glycidyl mixed diether of bis-(4-hydroxyphenyl)-2,2-propane and polymers thereof |
| US2516960A (en) * | 1948-08-19 | 1950-08-01 | Du Pont | Ethylene-alkylene oxide copolymers |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2511913A (en) * | 1950-06-20 | Compositions of resinous epoxides | ||
| NL59974C (enrdf_load_stackoverflow) * | 1943-06-16 | |||
| US2589245A (en) * | 1945-12-03 | 1952-03-18 | Devoe & Raynolds Co | Amide-epoxide compositions, etc. |
| US2494295A (en) * | 1946-09-13 | 1950-01-10 | Devoe & Raynolds Co | Compositions of resinous epoxides and aromatic sulfonamide-aldehyde condensates |
| NL68092C (enrdf_load_stackoverflow) * | 1947-06-11 | |||
| US2541027A (en) * | 1948-05-11 | 1951-02-13 | Shell Dev | Compositions of matter containing epoxy ethers and phosphorus-containing compounds |
| US2606810A (en) * | 1949-09-28 | 1952-08-12 | American Cyanamid Co | Treatment of wool-containing textile materials and products thereof |
-
0
- NL NLAANVRAGE7411923,A patent/NL174182B/xx unknown
- BE BE515900D patent/BE515900A/xx unknown
-
1951
- 1951-12-01 US US259504A patent/US2752269A/en not_active Expired - Lifetime
-
1952
- 1952-11-28 GB GB30258/52A patent/GB732573A/en not_active Expired
- 1952-11-29 DE DEN6423A patent/DE1024049B/de active Pending
- 1952-12-01 FR FR1071905D patent/FR1071905A/fr not_active Expired
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2455083A (en) * | 1945-05-08 | 1948-11-30 | Pacific Mills | Cellulose ethers of 3, 4 epoxy 1-butene and their oxidation products |
| US2464753A (en) * | 1947-03-25 | 1949-03-15 | Shell Dev | Allyl glycidyl mixed diether of bis-(4-hydroxyphenyl)-2,2-propane and polymers thereof |
| US2516960A (en) * | 1948-08-19 | 1950-08-01 | Du Pont | Ethylene-alkylene oxide copolymers |
Also Published As
| Publication number | Publication date |
|---|---|
| US2752269A (en) | 1956-06-26 |
| FR1071905A (fr) | 1954-09-07 |
| NL174182B (nl) | |
| GB732573A (en) | 1955-06-29 |
| BE515900A (enrdf_load_stackoverflow) |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE1024049B (de) | Verfahren zum Knitterfest- und Schrumpffestmachen von Textilien | |
| DE865589C (de) | Verfahren zur Veredlung von Cellulosefasern | |
| DE69712175T2 (de) | Verfahren zur Behandlung von Textilien aus Cellulosefasern mit Harzen | |
| DE2234751A1 (de) | Verfahren zur flammfestausruestung und steigerung der farbstoffaufnahmefaehgikeit von fasern | |
| DE2036610A1 (de) | Verfahren zur Herstellung von maßhalti gen und formbeständigen Kleidungsstücken mit Dauerbugelf alten | |
| DE971108C (de) | Verfahren zur Herstellung von Ausruestungseffekten auf cellulosehaltigen Geweben od. dgl. | |
| DE1105376B (de) | Verfahren zum Knitter- und Schrumpffestmachen von Textilien | |
| DE1469473A1 (de) | Verfahren zur Verbesserung der Aufnahmefaehigkeit bei Cellulosefasern | |
| DE2519136A1 (de) | Verfahren zum farbdrucken einer unterlage | |
| DE2715862C2 (de) | Verfahren zum Veredeln von Textilgut und stabiles Schaumprodukt zur Durchführung des Verfahrens | |
| DE1006828B (de) | Verfahren zur Erhoehung der Anfaerbbarkeit von Textilien aus synthetischen Fasern und Geweben | |
| CH318780A (de) | Beständige Imprägnierflüssigkeit zur Behandlung von Textilien | |
| DE954502C (de) | Verfahren zum Veredeln von Textilien | |
| DE1469293A1 (de) | Verfahren zur Erhoehung der Schrumpffestigkeit von Wolle | |
| DE707321C (de) | Verfahren zur Herstellung mehrlagiger Steifgewebe | |
| DE1184729B (de) | Verfahren zur Verbesserung der Wasch- und Abriebfestigkeit von faserigen cellulosehaltigen Textilien | |
| DE930746C (de) | Verfahren zur Behandlung von Textilstoffen, insbesondere aus regenerierter Cellulose | |
| DE3417239A1 (de) | Verfahren zur herstellung von filzfest ausgeruesteter, gegebenenfalls gefaerbter wolle | |
| DE903206C (de) | Verfahren zum Veredeln von Textilgut | |
| DE1469276C3 (de) | Verfahren zum Trocknen- und NaBknilterfestmachen von Textilien, die ganz oder überwiegend Regeneratcellulosefasern enthalten | |
| DE902367C (de) | Verfahren zur Verbesserung der Eigenschaften von Textilien | |
| DE948237C (de) | Verfahren zur Herstellung von waschfesten Praegungen auf Textilien | |
| AT270576B (de) | Mindestens teilweise aus Cellulosefasern bestehendes Textilgut mit verbesserten mechanischen Eigenschaften und Verfahren zur Herstellung desselben | |
| CH501097A (de) | Verfahren zur Verbesserung der Schmutzablösbarkeit von textilem Gut | |
| AT211784B (de) | Verfahren zur Erzielung von Knitter- und Schrumpffestigkeit bei Textilien aus Cellulosefasern, wie Baumwolle oder Zellwolle, durch Behandlung mit Aminoplasten |