CN1311357A - 聚酯织物 - Google Patents
聚酯织物 Download PDFInfo
- Publication number
- CN1311357A CN1311357A CN01103700A CN01103700A CN1311357A CN 1311357 A CN1311357 A CN 1311357A CN 01103700 A CN01103700 A CN 01103700A CN 01103700 A CN01103700 A CN 01103700A CN 1311357 A CN1311357 A CN 1311357A
- Authority
- CN
- China
- Prior art keywords
- acid
- emulsion
- organopolysiloxane
- alkyl
- preferred
- 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
- 229920000728 polyester Polymers 0.000 title claims abstract description 28
- 239000004744 fabric Substances 0.000 title claims abstract description 17
- 229920001296 polysiloxane Polymers 0.000 claims abstract description 41
- -1 polysiloxane Polymers 0.000 claims description 48
- 125000000217 alkyl group Chemical group 0.000 claims description 31
- 239000000839 emulsion Substances 0.000 claims description 30
- 238000000034 method Methods 0.000 claims description 12
- 239000000986 disperse dye Substances 0.000 claims description 2
- 239000000049 pigment Substances 0.000 claims description 2
- 238000007639 printing Methods 0.000 claims description 2
- 239000004753 textile Substances 0.000 abstract description 11
- 239000004902 Softening Agent Substances 0.000 description 28
- 239000002585 base Substances 0.000 description 27
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- 239000000203 mixture Substances 0.000 description 12
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 10
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 9
- 239000000975 dye Substances 0.000 description 9
- 229920000742 Cotton Polymers 0.000 description 8
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 7
- 239000003795 chemical substances by application Substances 0.000 description 7
- 235000009508 confectionery Nutrition 0.000 description 7
- 239000003995 emulsifying agent Substances 0.000 description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 7
- 239000004530 micro-emulsion Substances 0.000 description 7
- 239000000377 silicon dioxide Substances 0.000 description 7
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 150000001412 amines Chemical class 0.000 description 6
- 238000009980 pad dyeing Methods 0.000 description 6
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 5
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 5
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 5
- 229920002292 Nylon 6 Polymers 0.000 description 5
- 229920000297 Rayon Polymers 0.000 description 5
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 4
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 4
- 238000004043 dyeing Methods 0.000 description 4
- 150000002148 esters Chemical class 0.000 description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
- 239000000835 fiber Substances 0.000 description 4
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 150000007522 mineralic acids Chemical class 0.000 description 4
- XNLICIUVMPYHGG-UHFFFAOYSA-N pentan-2-one Chemical compound CCCC(C)=O XNLICIUVMPYHGG-UHFFFAOYSA-N 0.000 description 4
- CPRMKOQKXYSDML-UHFFFAOYSA-M rubidium hydroxide Chemical compound [OH-].[Rb+] CPRMKOQKXYSDML-UHFFFAOYSA-M 0.000 description 4
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical group N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 3
- 239000004593 Epoxy Substances 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- QOSMNYMQXIVWKY-UHFFFAOYSA-N Propyl levulinate Chemical compound CCCOC(=O)CCC(C)=O QOSMNYMQXIVWKY-UHFFFAOYSA-N 0.000 description 3
- 239000003513 alkali Substances 0.000 description 3
- 229920013822 aminosilicone Polymers 0.000 description 3
- HUCVOHYBFXVBRW-UHFFFAOYSA-M caesium hydroxide Inorganic materials [OH-].[Cs+] HUCVOHYBFXVBRW-UHFFFAOYSA-M 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 3
- QQZOPKMRPOGIEB-UHFFFAOYSA-N n-butyl methyl ketone Natural products CCCCC(C)=O QQZOPKMRPOGIEB-UHFFFAOYSA-N 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 150000002924 oxiranes Chemical class 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- DCKVNWZUADLDEH-UHFFFAOYSA-N sec-butyl acetate Chemical compound CCC(C)OC(C)=O DCKVNWZUADLDEH-UHFFFAOYSA-N 0.000 description 3
- 229920001187 thermosetting polymer Polymers 0.000 description 3
- RHLVCLIPMVJYKS-UHFFFAOYSA-N 3-octanone Chemical compound CCCCCC(=O)CC RHLVCLIPMVJYKS-UHFFFAOYSA-N 0.000 description 2
- HCFAJYNVAYBARA-UHFFFAOYSA-N 4-heptanone Chemical compound CCCC(=O)CCC HCFAJYNVAYBARA-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 2
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 2
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 2
- 241001062009 Indigofera Species 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- 239000004677 Nylon Substances 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 2
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 2
- 150000001721 carbon Chemical group 0.000 description 2
- 238000005352 clarification Methods 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- MLIREBYILWEBDM-UHFFFAOYSA-N cyanoacetic acid Chemical compound OC(=O)CC#N MLIREBYILWEBDM-UHFFFAOYSA-N 0.000 description 2
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- JXTHNDFMNIQAHM-UHFFFAOYSA-N dichloroacetic acid Chemical compound OC(=O)C(Cl)Cl JXTHNDFMNIQAHM-UHFFFAOYSA-N 0.000 description 2
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 150000002168 ethanoic acid esters Chemical class 0.000 description 2
- 125000004494 ethyl ester group Chemical group 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 239000011737 fluorine Substances 0.000 description 2
- CATSNJVOTSVZJV-UHFFFAOYSA-N heptan-2-one Chemical compound CCCCCC(C)=O CATSNJVOTSVZJV-UHFFFAOYSA-N 0.000 description 2
- NGAZZOYFWWSOGK-UHFFFAOYSA-N heptan-3-one Chemical compound CCCCC(=O)CC NGAZZOYFWWSOGK-UHFFFAOYSA-N 0.000 description 2
- QNVRIHYSUZMSGM-UHFFFAOYSA-N hexan-2-ol Chemical compound CCCCC(C)O QNVRIHYSUZMSGM-UHFFFAOYSA-N 0.000 description 2
- ZOCHHNOQQHDWHG-UHFFFAOYSA-N hexan-3-ol Chemical compound CCCC(O)CC ZOCHHNOQQHDWHG-UHFFFAOYSA-N 0.000 description 2
- 150000002430 hydrocarbons Chemical group 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- VIKNJXKGJWUCNN-XGXHKTLJSA-N norethisterone Chemical compound O=C1CC[C@@H]2[C@H]3CC[C@](C)([C@](CC4)(O)C#C)[C@@H]4[C@@H]3CCC2=C1 VIKNJXKGJWUCNN-XGXHKTLJSA-N 0.000 description 2
- 229920001778 nylon Polymers 0.000 description 2
- NMRPBPVERJPACX-UHFFFAOYSA-N octan-3-ol Chemical compound CCCCCC(O)CC NMRPBPVERJPACX-UHFFFAOYSA-N 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 238000010008 shearing Methods 0.000 description 2
- 229920005573 silicon-containing polymer Polymers 0.000 description 2
- 238000007592 spray painting technique Methods 0.000 description 2
- 238000010186 staining Methods 0.000 description 2
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- ULPMRIXXHGUZFA-UHFFFAOYSA-N (R)-4-Methyl-3-hexanone Natural products CCC(C)C(=O)CC ULPMRIXXHGUZFA-UHFFFAOYSA-N 0.000 description 1
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 1
- BMVXCPBXGZKUPN-UHFFFAOYSA-N 1-hexanamine Chemical compound CCCCCCN BMVXCPBXGZKUPN-UHFFFAOYSA-N 0.000 description 1
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 1
- QNVRIHYSUZMSGM-LURJTMIESA-N 2-Hexanol Natural products CCCC[C@H](C)O QNVRIHYSUZMSGM-LURJTMIESA-N 0.000 description 1
- MFGOFGRYDNHJTA-UHFFFAOYSA-N 2-amino-1-(2-fluorophenyl)ethanol Chemical compound NCC(O)C1=CC=CC=C1F MFGOFGRYDNHJTA-UHFFFAOYSA-N 0.000 description 1
- ZPVFWPFBNIEHGJ-UHFFFAOYSA-N 2-octanone Chemical compound CCCCCCC(C)=O ZPVFWPFBNIEHGJ-UHFFFAOYSA-N 0.000 description 1
- WLJVXDMOQOGPHL-PPJXEINESA-N 2-phenylacetic acid Chemical compound O[14C](=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-PPJXEINESA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- NMRPBPVERJPACX-QMMMGPOBSA-N 3-Octanol Natural products CCCCC[C@@H](O)CC NMRPBPVERJPACX-QMMMGPOBSA-N 0.000 description 1
- PFCHFHIRKBAQGU-UHFFFAOYSA-N 3-hexanone Chemical compound CCCC(=O)CC PFCHFHIRKBAQGU-UHFFFAOYSA-N 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- KBIWNQVZKHSHTI-UHFFFAOYSA-N 4-n,4-n-dimethylbenzene-1,4-diamine;oxalic acid Chemical compound OC(=O)C(O)=O.CN(C)C1=CC=C(N)C=C1 KBIWNQVZKHSHTI-UHFFFAOYSA-N 0.000 description 1
- PSBKJPTZCVYXSD-UHFFFAOYSA-N 5-methylheptan-3-one Chemical compound CCC(C)CC(=O)CC PSBKJPTZCVYXSD-UHFFFAOYSA-N 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 239000004258 Ethoxyquin Substances 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- WJYIASZWHGOTOU-UHFFFAOYSA-N Heptylamine Chemical compound CCCCCCCN WJYIASZWHGOTOU-UHFFFAOYSA-N 0.000 description 1
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 1
- JGFBQFKZKSSODQ-UHFFFAOYSA-N Isothiocyanatocyclopropane Chemical compound S=C=NC1CC1 JGFBQFKZKSSODQ-UHFFFAOYSA-N 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- RJUFJBKOKNCXHH-UHFFFAOYSA-N Methyl propionate Chemical compound CCC(=O)OC RJUFJBKOKNCXHH-UHFFFAOYSA-N 0.000 description 1
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical class CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 1
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- IOVCWXUNBOPUCH-UHFFFAOYSA-N Nitrous acid Chemical compound ON=O IOVCWXUNBOPUCH-UHFFFAOYSA-N 0.000 description 1
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Natural products OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical class [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000005864 Sulphur Substances 0.000 description 1
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 1
- TUMHNKUORWLQBE-UHFFFAOYSA-N [C].[Ar] Chemical compound [C].[Ar] TUMHNKUORWLQBE-UHFFFAOYSA-N 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 239000003619 algicide Substances 0.000 description 1
- 125000004450 alkenylene group Chemical group 0.000 description 1
- 125000004183 alkoxy alkyl group Chemical group 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 125000002521 alkyl halide group Chemical group 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 150000005840 aryl radicals Chemical class 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- RQPZNWPYLFFXCP-UHFFFAOYSA-L barium dihydroxide Chemical compound [OH-].[OH-].[Ba+2] RQPZNWPYLFFXCP-UHFFFAOYSA-L 0.000 description 1
- 229910001863 barium hydroxide Inorganic materials 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 239000011449 brick Substances 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical class CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- PWLNAUNEAKQYLH-UHFFFAOYSA-N butyric acid octyl ester Natural products CCCCCCCCOC(=O)CCC PWLNAUNEAKQYLH-UHFFFAOYSA-N 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 125000003262 carboxylic acid ester group Chemical group [H]C([H])([*:2])OC(=O)C([H])([H])[*:1] 0.000 description 1
- XTEGARKTQYYJKE-UHFFFAOYSA-N chloric acid Chemical compound OCl(=O)=O XTEGARKTQYYJKE-UHFFFAOYSA-N 0.000 description 1
- 229940005991 chloric acid Drugs 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000004567 concrete Substances 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 125000000392 cycloalkenyl group Chemical group 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 229960005215 dichloroacetic acid Drugs 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 239000004205 dimethyl polysiloxane Substances 0.000 description 1
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 1
- XQRLCLUYWUNEEH-UHFFFAOYSA-N diphosphonic acid Chemical compound OP(=O)OP(O)=O XQRLCLUYWUNEEH-UHFFFAOYSA-N 0.000 description 1
- 230000008034 disappearance Effects 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000003344 environmental pollutant Substances 0.000 description 1
- 229940093500 ethoxyquin Drugs 0.000 description 1
- DECIPOUIJURFOJ-UHFFFAOYSA-N ethoxyquin Chemical compound N1C(C)(C)C=C(C)C2=CC(OCC)=CC=C21 DECIPOUIJURFOJ-UHFFFAOYSA-N 0.000 description 1
- 235000019285 ethoxyquin Nutrition 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000006025 fining agent Substances 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000013355 food flavoring agent Nutrition 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 229930182478 glucoside Natural products 0.000 description 1
- 150000008131 glucosides Chemical class 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 210000004209 hair Anatomy 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 239000001307 helium Substances 0.000 description 1
- 229910052734 helium Inorganic materials 0.000 description 1
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 125000006038 hexenyl group Chemical group 0.000 description 1
- 150000002402 hexoses Chemical class 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- JISVIRFOSOKJIU-UHFFFAOYSA-N hexylidene Chemical group [CH2+]CCCC[CH-] JISVIRFOSOKJIU-UHFFFAOYSA-N 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 125000003253 isopropoxy group Chemical group [H]C([H])([H])C([H])(O*)C([H])([H])[H] 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 1
- 239000000347 magnesium hydroxide Substances 0.000 description 1
- 229910001862 magnesium hydroxide Inorganic materials 0.000 description 1
- 159000000003 magnesium salts Chemical class 0.000 description 1
- 229940017219 methyl propionate Drugs 0.000 description 1
- 230000003641 microbiacidal effect Effects 0.000 description 1
- 229940124561 microbicide Drugs 0.000 description 1
- 239000002855 microbicide agent Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 235000019799 monosodium phosphate Nutrition 0.000 description 1
- UUIQMZJEGPQKFD-UHFFFAOYSA-N n-butyric acid methyl ester Natural products CCCC(=O)OC UUIQMZJEGPQKFD-UHFFFAOYSA-N 0.000 description 1
- 125000003136 n-heptyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- IOQPZZOEVPZRBK-UHFFFAOYSA-N octan-1-amine Chemical compound CCCCCCCCN IOQPZZOEVPZRBK-UHFFFAOYSA-N 0.000 description 1
- WOFPPJOZXUTRAU-UHFFFAOYSA-N octan-4-ol Chemical compound CCCCC(O)CCC WOFPPJOZXUTRAU-UHFFFAOYSA-N 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- DPBLXKKOBLCELK-UHFFFAOYSA-N pentan-1-amine Chemical compound CCCCCN DPBLXKKOBLCELK-UHFFFAOYSA-N 0.000 description 1
- IGEIPFLJVCPEKU-UHFFFAOYSA-N pentan-2-amine Chemical compound CCCC(C)N IGEIPFLJVCPEKU-UHFFFAOYSA-N 0.000 description 1
- FDPIMTJIUBPUKL-UHFFFAOYSA-N pentan-3-one Chemical compound CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 description 1
- 150000002972 pentoses Chemical group 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
- 231100000719 pollutant Toxicity 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 229920000137 polyphosphoric acid Polymers 0.000 description 1
- 238000012805 post-processing Methods 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- BHRZNVHARXXAHW-UHFFFAOYSA-N sec-butylamine Chemical compound CCC(C)N BHRZNVHARXXAHW-UHFFFAOYSA-N 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- FDRCDNZGSXJAFP-UHFFFAOYSA-M sodium chloroacetate Chemical compound [Na+].[O-]C(=O)CCl FDRCDNZGSXJAFP-UHFFFAOYSA-M 0.000 description 1
- AJPJDKMHJJGVTQ-UHFFFAOYSA-M sodium dihydrogen phosphate Chemical class [Na+].OP(O)([O-])=O AJPJDKMHJJGVTQ-UHFFFAOYSA-M 0.000 description 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000009955 starching Methods 0.000 description 1
- UUCCCPNEFXQJEL-UHFFFAOYSA-L strontium dihydroxide Chemical compound [OH-].[OH-].[Sr+2] UUCCCPNEFXQJEL-UHFFFAOYSA-L 0.000 description 1
- 229910001866 strontium hydroxide Inorganic materials 0.000 description 1
- YBRBMKDOPFTVDT-UHFFFAOYSA-N tert-butylamine Chemical compound CC(C)(C)N YBRBMKDOPFTVDT-UHFFFAOYSA-N 0.000 description 1
- 125000002769 thiazolinyl group Chemical group 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 125000005023 xylyl group Chemical group 0.000 description 1
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- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
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- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
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- D06M15/03—Polysaccharides or derivatives thereof
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Abstract
一种包括至少一种有机聚硅氧烷及至少一种烷基多苷的聚酯织物。
Description
本发明涉及含有聚酯的织物。
众所周知者,用聚硅氧软化剂整理机织布、针织品或无纺(非织造)布等纺织品可产生一舒适、柔软手感。
氨基官能聚硅氧烷具有最佳的柔软手感。该等官能聚硅氧烷绝大多数可以微-或粗-乳化液的形式自市场上购得。
用作整理聚酯织物时,该等氨基官能聚硅氧烷具有严重缺点。其特别重大的缺失是对染色及印花耐洗性的破坏。
本发明的目的在克服既有技术的缺点。
本发明可实现此目的。
本发明提供的聚酯织物,其特征为包括至少一种有机聚硅氧烷及至少一种烷基多苷。
经发现,若所用软化剂是乳化液,该等乳化液的聚硅氧烷部分包括习知的氨基聚硅氧烷,而且依照本发明,该等氨基聚硅氧包含烷基多苷作为乳化剂时,则该上述缺点完全消失。
聚酯织物可能包括聚酯与棉、毛或其他材料的混合物(混纺织物)或仅包括聚酯,所制成的机织布、针织品或无纺布是用作衣服、桌布、覆盖物、帐蓬、运输器具,例如:布袋、帆布背包等。
通常聚酯织物是染以或印以分散染料且在高压及130℃温度下施以染色固色处理。
该等有机聚硅氧烷优选是有机聚硅氧烷(a),该等有机聚硅氧烷(a)在硅-碳相连的烃基上具有极性基,例如:氨基、铵基、环氧基、羟基、酰胺基、巯基、羧基及/或磺酸基、其盐类或酯类。
该等有机聚硅氧烷(a)优选具有化学通式(Ⅰ)
RnR'mSiO(4-n-m)/2 (Ⅰ)
其中
R优选是相同或不同、经取代或未经取代的烃基或在每种情况下均是具有1至18个碳原子烃氧基、氢原子或羟基,
R'优选是相同或不同硅-碳相连、经取代及含有极性基的烃基,
n是0、1、2或3的整数,
m是0、1、2或3的整数,
及n+m总和的平均值为1.8至2.2且m具有合适的值以使该聚有机硅氧烷具有至少一个R'基。
n+m总和的平均值优选为1.9至2.1。
烃基R的实例以烷基为佳,例如:甲基、乙基、正-丙基、异丙基、正-丁基、异-丁基、叔-丁基、正-戊基、异-戊基、新戊基、叔-戊基;己基,例如:正-己基;庚基,例如:正庚基;辛基,例如:正辛基及异辛基,例如:2,2,4-三甲基戊基;壬基,例如:正壬基;癸基,例如:正-癸基;十二基,例如:正-十二基;十八基,例如:正-十八基;烯基,例如:乙烯基,烯丙基及5-己烯-1-基;环烷基,例如:邻-、间-、对-甲苯基,二甲苯基及乙苯基;芳烷基,例如:苯甲基,α-苯乙基及β-苯乙基。
经取代或未经取代烃氧基R的实例优选是:经由一氧原子直接与一硅原子相连、依照前述实例经取代或未经取代的R基,尤其具有1至18个碳原子的烷氧基,特别是:甲氧基、乙氧基、正-丙氧基、异丙氧基及苯氧基。属于经取代或未经取代烃氧基的R基以不超过5%为佳。
优选的氨-官能R'基的实例是具有化学通式(Ⅱ)的基
-R1-[NR2(CH2)a]bNHR2 (Ⅱ)
且与无机酸或羧酸反应可制得其铵盐,其中
R1优选是一两价C1-至C18-烃基,
R2优选是一氢原子或经氟取代、氯取代或溴取代的C1-至C18-烃基,
a是2、3、4、5或6及
b是0、1、2、3或4。
两价C1-至C18-烃基R1的优选实例是饱和的直链或分枝链或环烯基,例如:亚甲基、亚乙基以及亚丙基、亚丁基、亚戊基、亚己基、2-甲基亚丙基、环型亚己基及亚十八基、或不饱和的亚烯基或亚芳基,例如:亚己烯基及亚苯基,其中亚正-丙基及2-甲基亚丙基最为优选。
烃基R2的优选实例是R的实例。经卤素-取代的烃基R3的实例是卤烷基,例如:3,3,3-三氟-正-丙基,2,2,2,2’2’,2’-六氟异丙基、七氟异丙基及卤芳基,例如:邻-、间-、及对-氯苯基。
在前述化学通式(Ⅱ)中,优选
R1是一两价C2-至C6-烃基,
R2 是一氢原子、一甲基或环己基,
a 是2或3及
b 是0或1。
最优选的是直线型聚二甲基硅氧烷,其可包含的R基不超过5%C1-至C3-烷氧基或终端羟基以及甲基。在该等聚二甲基硅氧烷中R1基优选是
H2N(CH2)2NH(CH2)3-,H2N(CH2)2NHCH2CH(CH3)CH2-,
可与前述氨-官能烃基反应生成对应铵官能基的优选无机酸是:盐酸、过氯酸、硫酸、亚硫酸、硝酸、亚硝酸、氢氟酸、磷酸、二磷酸及多磷酸。优选的合适羧酸实例是:甲酸、乙酸、丙酸、丁酸、柠檬酸、三氯乙酸、二氯乙酸及氯乙酸、三氟乙酸、氰乙酸、苯乙酸、苯甲酸、间-及对-硝基苯甲酸、乙二酸、丙二酸及乳酸。其中以由乙酸制得的铵官能烃基最为优选。
优选的氨官能基实例是:γ-乙酰基酰胺基丙基、部分或全部乙酰化的β-氨基乙基-γ-氨基丙基。
其中A是一烷基、烷氧基烷基、芳香基或烷芳基。
环氧-官能有机聚硅氧烷(a)的优选环氧化物数为0.5至0.001(当量/100克),尤以0.2至0.01(当量/100克)更为优选。环氧-官能有机聚硅氧烷的环氧化物数是指100克有机聚硅氧烷(a)内所含环氧化物的当量数(例如:环氧化物基的摩尔数)。
优选羧基-官能R2基的实例是具有化学通式(Ⅴ)的基
-X-(COOH)p (Ⅴ)
及其与碱反应所制得的盐类,其中
X是一直线型、分枝型脂族、芳香或混合脂族及芳香烃基,该等基的碳结构可能由两价的硫、氧或羧酸酯基间断及
p是1或2
特别优选的羧基官能R′基是下列诸基
-(CH2)4-10-COOH,
-CH2CH(CH3)COOH,
-(苯基)-COOH,
-CH2CHR3-S-CH2-COOH,
其中R3优选是一氢原子、一甲基或乙基,
特别优选的羧基-官能R′基是下列诸基
-(CH2)10-COOH,
-CH2CH(CH3)COOH,及
-(CH2)2-S-CH2-COOH。
与包括R′基的羧基官能有机聚硅氧烷反应的优选碱实例是:氨、胺、碱金属及碱土金属的氢氧化物,例如:氢氧化锂(LiOH)、氢氧化钠(NaOH)、氢氧化钾(KOH)、氢氧化铷(RbOH)、氢氧化铯(CsOH)、氢氧化镁(Mg(OH)2)、氢氧化钙(Ca(OH)2)、氢氧化锶(Sr(OH)2)及氢氧化钡(Ba(OH)2)。
羧基-官能有机聚硅氧烷(a)的优选酸值为1至100(毫克KOH/克),尤以5至50更优选及10至30量优选。羧基-官能有机聚硅氧烷(a)的酸值是指中和1克羧基-官能有机聚硅氧烷(a)内所含游离酸需要氢气化钾的毫克数。
R以甲基、乙基、苯基、甲氧基及/或乙烯基较为优选。由于获得较为容易,R基的50%为甲基较佳,尤以R基的至少80%为甲基最佳。
在工业上,可能用一种有机众硅氧烷(a),尤以具有化学通式(Ⅰ)的有机采硅氧烷(a);亦可能使用许多种有机聚硅氧烷。
乳化液内所用的有机聚硅氧烷(混合物)优选是液体。尤其本发明方法中断用的有机聚硅氧烷,在25℃温度下的粘度各为100毫帕斯卡·秒至1,000,000毫帕斯卡·秒。
制造本发明乳化液内优选使用的铵-官能有机聚硅氧烷(a)所用的氨基,官能有机聚硅氧烷,其胺值以0.1至3.0为佳,尤以0.2至0.9更佳。一氨基官能物质的胜值是由滴定1克氨基-官能物质所耗1含量浓度盐酸的立方厘米数而测得。
举例言之,有用的烷基多苷包含具有化学通式(Ⅵ)的欧洲专利EP-A418479烷基多苷
R″-O-Zo (Ⅵ)
其中
R″是一直线型或分枝型、饱和或不饱和的烷基,平均以具有8至24个碳原子者为佳,尤以8至16个碳原子更佳,及
Zo是一低聚糖苷基,平均o=1至10个(尤以1至5个更佳)己糖或戊糖单元或其混合物。
特别优选的烷基多苷具有一平均8至14个碳原子的饱和烷基且平均糖苷化程度n为1.1至3。
本发明更提供一处理聚酯织物的方法,其中包括应用至少一种有机聚硅氧烷及至少一种烷基多苷。
聚酯织物的处理以采用一种水性乳化液为佳,该水性乳化液的主要成分为
a)100份重量比的有机聚硅氧烷(该等有机聚硅氧烷的硅-碳连接的氩碳基上优选有一极性基)及
b)优选高达150份重量比的烷基多苷。
该等有机聚硅氧烷及烷基多苷具有以上所示的意义。
与聚二甲基硅氧烷油类、聚二苯基硅氧炕油类及烷基多苷类的水性乳化液不同的是:本发明所用的乳化液对异质电解质(例如:镁盐及钛盐)的稳定性高于用烷基聚乙二醇醚作为乳化剂的对应乳化液者。
本发明所用乳化液含有较少量的乳化剂,尤其每100份重量比含有极性基的有机聚硅氧烷(a)为5至100份重量比烷基多苷(b)。
本发明所用乳化液具有一不连续油相(其中含有极性基的有机聚硅氧烷(a))及一连续水相。
有机聚硅氧烷(a)及连续水相的比例变化范围甚广,视乳化液内的预期固体含量及本发明所用微乳化液而定。有机聚硅氧烷(a)占乳化液总重量的比例以20至70%重量比为佳,尤以40至60%重量比更佳。
本发明所用乳化液的平均粒径以不超过1微米为佳,尤以不超过300毫微米更佳。本发明所用微乳化液的平均粒径以不超过150毫微米为佳,尤以不超过20毫微米更佳。在本申请全文中“乳化液”一词亦包含微乳化液。“微乳化液”一词仅涉及平均粒径不超过150毫微米的透明或光清澈的乳化液。以往来曾述及用烷基多苷作为乳化剂的有机聚硅氧烷微乳化液。
举例言之,本发明所用乳化液(尤其微乳化液)亦可能包含辅助界面活性剂(使用量以0至30份重量比为佳,尤以不起过20份重量比更佳,均是以100份重量比有机聚硅氧烷(a)为准)以减小粒径及减少烷基多苷(b)的需求量。
辅助界面活性剂是中等摩尔质量的极性化合物,例如:具有4至8个碳原子的优选醇类,合适的乙二醇醚类、胺类、酯类或酮类。
特别合适的辅助界面活性剂优选实例是:1-丁醇、2-丁醇、2-甲基-2-丙醇、1-戊醇、2-戊醇、3-戊醇、1-己醇、2-己醇、3-己醇、1-庚醇、2-庚酵、3-庚醇、4-庚醇、1-辛醇、2-辛醇、3-辛醇及4-辛醇;甘二醇一甲基、一乙基及一丁基醚;1-氨基丁烷、2-氨基丁烷、2-氨基-2-甲基丙烷、1-氨基戊烷、2-氨基戊烷、1-氨基己烷、1-氨基庚烷及1-氨基辛烷;乙酸乙酯、丙酯、异丙酯、丁酯、异丁酯、戊酯、异戊酯及己酯;丙酸甲酯、乙酯及叔丁酯;丁酸甲酯、乙酯、丙酯及丁酯;2-丁酮、2-戊酮、3-戊酮、4-甲基-2-戊酮、2-己酮、3-己酮、2-庚酮、3-庚酮、4-庚酮、5-甲基-3-庚酮、2-辛酮及3-辛酮。
更优选辅助界面活性剂的实例是:上述具有C5-至C8-链实例中的1-烷醇类、甘二醇-丁基醚、甘二醇二甲基醚及甘二醇二乙基醚、乙醚丙酯、丁酯及戊酯以及2-戊酮。
最优选辅助界面活性剂的实例是:1-戊醇、1-己醇及1-辛醇、甘二醇-丁基醚、甘二醇二甲基醚及乙酸丁酯。
本发明所用乳化液除含有有机众硅氧烷(a)、烷基多苷(b)、水及选择性界面活性剂之外,亦可能包含若干添加剂。该等特别优选添加剂的实例是:杀细菌剂、杀真菌剂、除藻剂、杀微生物剂、香味剂、腐蚀抑制剂、染料、颜料、稠化剂及填料。本发明所用乳化液内添加剂的含量以0至1%重量为佳,尤以0至0.2%重量比更佳(均是以制妥乳化液的总重量为基准)。
本发明所用乳化液全部成分的混合作用,可利用乳化器或连同低剪力搅拌、依照任何顺序实施。但优选的程序是:首先将有机跟硅氧烷(a)、烷基多苷(b)及水制成一均匀混合物,随后在不施加高剪力的情况下,将辅界面活性剂及添加剂(假若使用)搅入该混合物内。
施于各成分或混合物的压力优选是(大气)压力,该压力可能因诸成分的混合作用面升高;对应的环境温度优选是(室)温,该温度可能因诸成分的混合作用而升高。
本发明所用乳化液内优选包含的铵基-官能有机聚硅氧烷(a)可藉添加无机酸或羧酸于对应氨基-官能有机众硅氧烷内制得。将酸添加于有机采硅氧烷(a)内的工作可在使用有机泵硅氧烷(a)之前实施。
但在利用特别优选氨基-及/或铵基官能有机采硅氧烷(a)以制备本发明所用乳化液的特别优选具体实施例内,藉添加上述无机酸及/或羧酸(尤其乙酸),于混合有机聚硅氧烷(a)、烷基多苷(b)及水的过程中即就地产生铵-官能基。
原则上本发明所用乳化液可用前此制备乳化液所用的任何紊流混合器制得。可用的混合器实例是:搅拌器,例如:叶片、条棒、锚状、栅状、螺杆、旋浆、碟状、叶轮、涡轮、行星式等搅拌器。单-及双-螺杆混合器、混合涡轮器、胶体研磨器、超音波混合器、直排混合器、泵、均化器,例如:高压、涡轮及环圈均化器。
不同式样的聚酯(PES)是用习知灵敏的不同染料,在温度130℃及无载体的情况下施以印花或喷染,历时30至45分钟。染色后,藉轧染法或浸染法散以不同聚硅氧软化剂。继之,在185℃温度下加以烘干及热固,历时60秒钟。随后在60℃温度下,将所制试样连同一多灵纤维条带(乙酸酯、棉花、尼龙6.6;聚酯、聚丙烯腈及羊毛)施以CA4马克仕及史宾塞耐洗试验。
评估的标准均是依照灰标(德国工业标准DIN 54002)测定各种不同织物的着色度及染色织物的色调变化。评定的结果共分为1至5等,其中5等最佳及1等最差。在此评估作业中,将乙酸酯及尼龙的着色度加以测定,盖因该等底布(被染物)最具表现力。
以下所有百分率皆是重量比。
所用软化剂(WM)为:
WM1:乳状乳化液,含有33%氦基聚硅氧(胺值为0.3,粘度为1000,具有结构单元Si-C33H6-NH-C2H4-NH2)及6%脂族醇乙氧基化物(C13含氧醇,具有6至8个环氧乙烷单元),平均粒径约为130毫微米。
WM2:微乳化液,含有33%氨基聚硅氧(如同WM1),13%脂族醇乙氧基化物(C13脂族醇,具有6至8个环氧乙烷单元)及5%辅乳化剂(丁基甘二醇),平均粒径约为30毫微米。
WM3:粗乳化液,含有35%氨基聚硅氧(胺值为0.15,粘度为5000,结构请参阅WM1),4%脂族醇乙氧基化物(C13脂族醇,具有10个环氧乙烷单元),平均粒径约为180毫微米。
WM4:浓缩乳化液,含有40%氨基聚硅氧烷(如同WM1),6%脂族醇乙氧基化物(C13脂族醇,具有3个环氧乙烷单元),18%AEPO(壬基酚,具有10个环氧乙烷单元)及6%辅乳化刮(丁基乙二醇),平均粒径为25毫微米(经以1∶5稀释后)。
WM5:所发明的乳化液,包括17%氨基聚硅氧烷(胺值为0.6,粘度为1000,结构单元请参阅WM1),6%烷基多苷,每个分子附有1.8个糖单元的C8至C10烷基,粒径约为250毫微米。
实施例1:
将具有下列配方的印花浆均匀地印在聚酯织物(PES长丝或丝状纤维)上:
500克分散储备液+卡尔康
20克染料:大爱尼克斯红EFB(代斯塔尔)
2克磷酸一钠
15克伊加纳耳PS(克拉菌特澄清剂)
463克其他成分
1公斤
藉施以热溶胶将该印花加以固色(210℃,60秒钟),之后在60℃温度下加以清洗。继之用5克/升的碱及3克/升的亚硫酸氢盐予以还原澄清,随后在80℃温度下加以清洗。于一轧染机上,用软化剂将该试样加以整理(上浆)至纤维吸液率达到65%:
A)15克/升软化剂1
B)15克/升软化剂2
C)15克/升软化剂4
D)15克/升软化剂5
E)15克/升软化剂5
F)水
G)未经处理者
在185℃温度下,依序将A至G的试样加以烘干及热固着,历时60秒钟。
依照上述C4A的方法,将该等试样连同该多重纤维条带加以洗涤。
CA=粘胶(液)纤维
CO=棉花
PA6.6=尼龙-6.6
PES=聚酯
结果:
A | B | C | D | E | F | G | |
色调变化 | 4-5 | 4-5 | 4-5 | 4-5 | 4-5 | 4-5 | 4-5 |
粘胶纤维 | 2-3 | 2 | 1-2 | 3 | 3 | 3 | 3-4 |
棉花 | 4-5 | 4 | 3-4 | 5 | 5 | 5 | 5 |
尼龙-6.6 | 2-3 | 2 | 1-2 | 3 | 3 | 3 | 3-4 |
聚酯 | 4-5 | 4 | 3-4 | 5 | 5 | 5 | 5 |
实施例2:
利用由代斯塔尔大爱尼克斯系列形成的下列染料组合物(习知该等组合物固化极为快速)将聚酯织物[由卷曲变形纱(加工纱)制成,染色前未固化]加以喷染;
红色:大爱尼克斯黄4G 0.23%+大爱尼克斯红SE 3B 051%+大爱尼克斯红K2B 0.54%
黑色:大爱尼克斯橙K3G 0.12%+大爱尼克斯红S2G 0.2%+大爱尼克斯黑RXNFS 200%其中的3.5%
该染色工作是在有1克/升分散剂PN及2克/升乙酸纳存在、温度130℃及氢标值4.5(用乙酸设定)的情况下实施,历时45分钟。
还原澄清工作(后处理)是用5克/升NaOH38℃波美度及3克/升亚硫酸氢钠、在80℃温度下实施,历时15分钟。
在程序1内,于一轧染机上,在氢标值为6.0的情况下,用下列液体整理该等试样至纤维吸液率达到65%:
A)15克/升软化剂1
B)15克/升软化剂2
C)15克/升软化剂4
D)15克/升软化剂5
E)15克/升软化剂5
F)水
G)未经处理者
程序2是在60℃温度下以浸染法实施,历时20分钟。
A)1.5%软化剂1
B)1.5%软化剂2
C)1.5%软化剂4
D)1.5%软化剂5
E)3.0%软化剂5
F)水
G)未经处理者
依照惯例,在185℃温度下,将其烘干及热固,历时1分钟。连同DW多重纤维条带,依照所述方式,施以马克仕及史宾塞洗涤测得下列诸值:
染红 轧染/浸染法
A | B | C | D | E | F | G | |
粘胶纤维 | 2-3/2-3 | 2/2 | 1-2/1-2 | 3/3 | 3/3 | 3/3 | 3/3 |
棉花 | 5/5 | 4-5/4-5 | 4/4 | 5/5 | 5/5 | 5/5 | 5/5 |
尼龙-6.6 | 3/3-4 | 2-3/2-3 | 2/2 | 4/4 | 4/4 | 4/4 | 4/4 |
聚酯 | 4-5/4-5 | 4/4 | 3-4/3-4 | 5/5 | 5/5 | 5/5 | 5/5 |
染黑 轧染/浸染法
A | B | C | D | E | F | G | |
粘胶纤维 | 2-3/3 | 2/2 | 1-2/2 | 3-4/3-4 | 3-4/3-4 | 3-4/3-4 | 3-4/3-4 |
棉花 | 4-5/4-5 | 4/4 | 3-4/3-4 | 4-5/4-5 | 4-5/4-5 | 4-5/4-5 | 5/5 |
尼龙-6.6 | 3/4 | 2-3/3 | 2/2 | 4/4-5 | 4/4-5 | 4/4-5 | 4-5/4-5 |
聚酯 | 4-5/4-5 | 3-4/3-4 | 3/3 | 4-5/4-5 | 4-5/4-5 | 4-5/4-5 | 5/5 |
实施例3:
将实施例2的程序重复一遍,用0.98%的大爱尼克斯深蓝KR+大爱尼克斯黑KB0.31%将聚酯织物染蓝。该等试样在程序Ⅰ中施以轧染及在程序Ⅱ中施以浸染。所用软化剂为:
A)15克/升或1.5%软化剂1
B)15克/升或1.5%软化剂2
C)15克/升或1.5%软化剂3
D)15克/升或1.0%软化剂4
E)15克/升或3.0%软化剂5
F)水
G)未经处理者
轧染工作是经实施至纤维吸液率达到65%。浸染工作是在温度60℃及氢标值为6的情况下实施,历时20分钟。热固工作是依照惯例在185℃温度下实施,历时1分钟。
结果(蓝)轧染/浸染法
A | B | C | D | E | F | G | |
粘胶纤维 | 3/3 | 2-3/3 | 3/3 | 2/2 | 4/4 | 4/4 | 4/4 |
棉花 | 4/4 | 4/4 | 4/4 | 3-4/3-4 | 4-5/4-5 | 4-5/4-5 | 4-5/4-5 |
尼龙-6.6 | 2-3/3 | 2-3/3 | 3/2-3 | 2/2 | 3-4/3-4 | 3-4/3-4 | 4/4 |
聚酯 | 4/4 | 3/3 | 4/4 | 3/3 | 4-5/4-5 | 4-5/4-5 | 4-5/4-5 |
由该等实验系列所得的明显结果及结论是:
与经水处理的织物相较,经本发明软化剂处理的试样的耐洗度实质上并未恶化。
相反地,传统式软化剂产生的劣化作用高达2个等级,并且发现等级劣化作用与乙氧化乳化剂具体含量间的相互关系。
Claims (6)
1、一种含有聚酯的织物,其特征为包括至少一种有机聚硅氧烷及至少一种烷基多苷。
2、根据权利要求1的含有聚酯的织物,其中包括一分散性染料或印花颜料。
3、根据权利要求1或2的含有聚酯的织物,其中该有机聚硅氧烷是一氨基-官能有机聚硅氧烷。
4、根据权利要求1至3中之一项或多项的含有聚酯的织物,其中有机聚硅氧烷与该烷基多苷的重量比为10∶1至0.5∶1。
5、一种用以处理如权利要求1至4中之一的含有聚酯的织物的方法,其中包括应用至少一种有机聚硅氧烷及至少一种烷基多苷。
6、根据权利要求5的方法,其中所用的至少一种有机聚硅氧烷及至少一种烷基多苷是呈乳化液的形式。
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DE10005855.8 | 2000-02-10 | ||
DE10005855A DE10005855A1 (de) | 2000-02-10 | 2000-02-10 | Flächengebilde aus Polyester |
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CN1311357A true CN1311357A (zh) | 2001-09-05 |
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CN01103700A Pending CN1311357A (zh) | 2000-02-10 | 2001-02-09 | 聚酯织物 |
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US (1) | US20010018305A1 (zh) |
EP (1) | EP1127975A1 (zh) |
KR (1) | KR20010082092A (zh) |
CN (1) | CN1311357A (zh) |
BR (1) | BR0100459A (zh) |
DE (1) | DE10005855A1 (zh) |
HK (1) | HK1040268A1 (zh) |
ID (1) | ID29216A (zh) |
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JP7323053B2 (ja) * | 2020-03-10 | 2023-08-08 | 京セラドキュメントソリューションズ株式会社 | インクジェット用処理液、インクジェット捺染装置、及びインクジェット捺染方法 |
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EP0094118B2 (en) * | 1982-05-10 | 1993-04-21 | THE PROCTER & GAMBLE COMPANY | Low phosphate laundry detergent compositions |
DE3925846A1 (de) * | 1989-08-04 | 1991-02-14 | Huels Chemische Werke Ag | Emulgatoren zur herstellung von lagerstabilen, waessrigen polysiloxan- bzw. polysiloxan-paraffinoel-emulsionen |
DE4131551A1 (de) * | 1991-09-21 | 1993-03-25 | Pfersee Chem Fab | Waessrige dispersionen von stickstoffhaltigen polysiloxanen |
DE4133551A1 (de) * | 1991-10-10 | 1993-04-15 | Kloeckner Humboldt Deutz Ag | Verfahren und vorrichtung zur direktsaat waehrend eines erntevorgangs |
DE4306796A1 (de) * | 1993-03-04 | 1994-09-08 | Wacker Chemie Gmbh | Emulsionen polare Gruppen enthaltender Organopolysiloxane mit Alkylpolyglykosiden als Emulgatoren |
DE4328917A1 (de) * | 1993-08-27 | 1995-03-02 | Wacker Chemie Gmbh | Herstellung von Organopolysiloxan-Microemulsionen |
DE19538751A1 (de) * | 1995-10-18 | 1997-04-24 | Huels Chemische Werke Ag | Entschäumerdispersionen für wäßrige Tensidsysteme |
DE19721699A1 (de) * | 1997-05-23 | 1998-11-26 | Huels Silicone Gmbh | Aminosiliconöl-Microemulsionen |
DE19722680A1 (de) * | 1997-05-30 | 1998-12-03 | Wacker Chemie Gmbh | Siliconweichmacher für Jeans |
-
2000
- 2000-02-10 DE DE10005855A patent/DE10005855A1/de not_active Ceased
- 2000-12-21 EP EP20000127958 patent/EP1127975A1/de not_active Withdrawn
-
2001
- 2001-02-05 ID ID20010112D patent/ID29216A/id unknown
- 2001-02-06 US US09/778,196 patent/US20010018305A1/en not_active Abandoned
- 2001-02-08 BR BR0100459A patent/BR0100459A/pt not_active IP Right Cessation
- 2001-02-09 CN CN01103700A patent/CN1311357A/zh active Pending
- 2001-02-09 KR KR1020010006365A patent/KR20010082092A/ko not_active Application Discontinuation
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2002
- 2002-03-01 HK HK02101597.3A patent/HK1040268A1/zh unknown
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Publication number | Publication date |
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BR0100459A (pt) | 2001-09-11 |
EP1127975A1 (de) | 2001-08-29 |
ID29216A (id) | 2001-08-16 |
HK1040268A1 (zh) | 2002-05-31 |
US20010018305A1 (en) | 2001-08-30 |
KR20010082092A (ko) | 2001-08-29 |
DE10005855A1 (de) | 2001-08-23 |
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