JP6515715B2 - A erosion-treated woven or knitted fabric containing a modified polyester fiber and a method for producing the same - Google Patents
A erosion-treated woven or knitted fabric containing a modified polyester fiber and a method for producing the same Download PDFInfo
- Publication number
- JP6515715B2 JP6515715B2 JP2015141163A JP2015141163A JP6515715B2 JP 6515715 B2 JP6515715 B2 JP 6515715B2 JP 2015141163 A JP2015141163 A JP 2015141163A JP 2015141163 A JP2015141163 A JP 2015141163A JP 6515715 B2 JP6515715 B2 JP 6515715B2
- Authority
- JP
- Japan
- Prior art keywords
- fiber
- knitted fabric
- woven
- polyester fiber
- modified polyester
- 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.)
- Active
Links
- 239000000835 fiber Substances 0.000 title claims description 159
- 239000004744 fabric Substances 0.000 title claims description 118
- 229920000728 polyester Polymers 0.000 title claims description 110
- 238000004519 manufacturing process Methods 0.000 title claims description 8
- 230000003628 erosive effect Effects 0.000 title description 10
- -1 polytrimethylene terephthalate Polymers 0.000 claims description 50
- 238000000034 method Methods 0.000 claims description 49
- 239000003795 chemical substances by application Substances 0.000 claims description 48
- 230000004580 weight loss Effects 0.000 claims description 33
- 238000007790 scraping Methods 0.000 claims description 24
- 238000012545 processing Methods 0.000 claims description 22
- 238000010438 heat treatment Methods 0.000 claims description 16
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 12
- 210000004177 elastic tissue Anatomy 0.000 claims description 10
- 229920002994 synthetic fiber Polymers 0.000 claims description 9
- 239000012209 synthetic fiber Substances 0.000 claims description 9
- 229920006306 polyurethane fiber Polymers 0.000 claims description 8
- LLLVZDVNHNWSDS-UHFFFAOYSA-N 4-methylidene-3,5-dioxabicyclo[5.2.2]undeca-1(9),7,10-triene-2,6-dione Chemical compound C1(C2=CC=C(C(=O)OC(=C)O1)C=C2)=O LLLVZDVNHNWSDS-UHFFFAOYSA-N 0.000 claims description 7
- 125000001931 aliphatic group Chemical group 0.000 claims description 7
- 125000004432 carbon atom Chemical group C* 0.000 claims description 7
- 230000014759 maintenance of location Effects 0.000 claims description 7
- 239000000470 constituent Substances 0.000 claims description 6
- 125000003118 aryl group Chemical group 0.000 claims description 5
- 229910052751 metal Inorganic materials 0.000 claims description 5
- 239000002184 metal Substances 0.000 claims description 5
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 claims description 5
- 239000004952 Polyamide Substances 0.000 claims description 4
- 229920002647 polyamide Polymers 0.000 claims description 4
- 229920002215 polytrimethylene terephthalate Polymers 0.000 claims description 4
- 229920002972 Acrylic fiber Polymers 0.000 claims description 3
- 229920000098 polyolefin Polymers 0.000 claims description 3
- 229920001748 polybutylene Polymers 0.000 claims 1
- 239000002759 woven fabric Substances 0.000 claims 1
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 42
- 208000016261 weight loss Diseases 0.000 description 33
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 27
- 230000000052 comparative effect Effects 0.000 description 24
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 21
- 239000003513 alkali Substances 0.000 description 21
- 238000007639 printing Methods 0.000 description 18
- 229910000029 sodium carbonate Inorganic materials 0.000 description 14
- 235000011121 sodium hydroxide Nutrition 0.000 description 14
- 239000007864 aqueous solution Substances 0.000 description 13
- 235000017550 sodium carbonate Nutrition 0.000 description 13
- 238000005406 washing Methods 0.000 description 13
- 238000004043 dyeing Methods 0.000 description 12
- 125000002947 alkylene group Chemical group 0.000 description 11
- 235000014113 dietary fatty acids Nutrition 0.000 description 11
- 239000000194 fatty acid Substances 0.000 description 11
- 229930195729 fatty acid Natural products 0.000 description 11
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 10
- 239000004094 surface-active agent Substances 0.000 description 10
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 9
- 125000002091 cationic group Chemical group 0.000 description 7
- 239000002736 nonionic surfactant Substances 0.000 description 7
- 235000011118 potassium hydroxide Nutrition 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- STIAPHVBRDNOAJ-UHFFFAOYSA-N carbamimidoylazanium;carbonate Chemical compound NC(N)=N.NC(N)=N.OC(O)=O STIAPHVBRDNOAJ-UHFFFAOYSA-N 0.000 description 6
- 230000007423 decrease Effects 0.000 description 6
- 208000002925 dental caries Diseases 0.000 description 6
- 238000011156 evaluation Methods 0.000 description 6
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- KWIUHFFTVRNATP-UHFFFAOYSA-N Betaine Natural products C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 5
- 239000002253 acid Substances 0.000 description 5
- 239000003945 anionic surfactant Substances 0.000 description 5
- 238000001035 drying Methods 0.000 description 5
- 229910000027 potassium carbonate Inorganic materials 0.000 description 5
- 235000011181 potassium carbonates Nutrition 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 4
- 238000004140 cleaning Methods 0.000 description 4
- 238000005260 corrosion Methods 0.000 description 4
- 230000007797 corrosion Effects 0.000 description 4
- 230000018044 dehydration Effects 0.000 description 4
- 238000006297 dehydration reaction Methods 0.000 description 4
- 150000004665 fatty acids Chemical class 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 150000005846 sugar alcohols Polymers 0.000 description 4
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 229910019142 PO4 Inorganic materials 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 229960003237 betaine Drugs 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 229920001971 elastomer Polymers 0.000 description 3
- 239000010452 phosphate Substances 0.000 description 3
- 229920001707 polybutylene terephthalate Polymers 0.000 description 3
- 229920000139 polyethylene terephthalate Polymers 0.000 description 3
- 239000005020 polyethylene terephthalate Substances 0.000 description 3
- 238000004513 sizing Methods 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 150000003871 sulfonates Chemical class 0.000 description 3
- VVJKKWFAADXIJK-UHFFFAOYSA-N Allylamine Chemical compound NCC=C VVJKKWFAADXIJK-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 101100002917 Caenorhabditis elegans ash-2 gene Proteins 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
- SUZRRICLUFMAQD-UHFFFAOYSA-N N-Methyltaurine Chemical compound CNCCS(O)(=O)=O SUZRRICLUFMAQD-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 239000001361 adipic acid Substances 0.000 description 2
- 235000011037 adipic acid Nutrition 0.000 description 2
- 239000002280 amphoteric surfactant Substances 0.000 description 2
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 2
- 239000003093 cationic surfactant Substances 0.000 description 2
- 238000007334 copolymerization reaction Methods 0.000 description 2
- JQVDAXLFBXTEQA-UHFFFAOYSA-N dibutylamine Chemical compound CCCCNCCCC JQVDAXLFBXTEQA-UHFFFAOYSA-N 0.000 description 2
- 239000003925 fat Substances 0.000 description 2
- 238000007641 inkjet printing Methods 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 229920001225 polyester resin Polymers 0.000 description 2
- 239000004645 polyester resin Substances 0.000 description 2
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 2
- 239000013585 weight reducing agent Substances 0.000 description 2
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
- RYYXDZDBXNUPOG-UHFFFAOYSA-N 4,5,6,7-tetrahydro-1,3-benzothiazole-2,6-diamine;dihydrochloride Chemical compound Cl.Cl.C1C(N)CCC2=C1SC(N)=N2 RYYXDZDBXNUPOG-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 241000416162 Astragalus gummifer Species 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- 229920001353 Dextrin Polymers 0.000 description 1
- 239000004375 Dextrin Substances 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- 229920000161 Locust bean gum Polymers 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 238000005903 acid hydrolysis reaction Methods 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 238000005904 alkaline hydrolysis reaction Methods 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 150000001483 arginine derivatives Chemical class 0.000 description 1
- 229940077388 benzenesulfonate Drugs 0.000 description 1
- 238000003763 carbonization Methods 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 150000001734 carboxylic acid salts Chemical class 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000012790 confirmation Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 235000019425 dextrin Nutrition 0.000 description 1
- 125000005266 diarylamine group Chemical group 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- WEHWNAOGRSTTBQ-UHFFFAOYSA-N dipropylamine Chemical compound CCCNCCC WEHWNAOGRSTTBQ-UHFFFAOYSA-N 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- GRWZHXKQBITJKP-UHFFFAOYSA-L dithionite(2-) Chemical compound [O-]S(=O)S([O-])=O GRWZHXKQBITJKP-UHFFFAOYSA-L 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000009415 formwork Methods 0.000 description 1
- MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical compound C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 238000009940 knitting Methods 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 239000000711 locust bean gum Substances 0.000 description 1
- 235000010420 locust bean gum Nutrition 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- 229940049964 oleate Drugs 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 239000011022 opal Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 229920001495 poly(sodium acrylate) polymer Polymers 0.000 description 1
- 229920001515 polyalkylene glycol Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 230000001603 reducing effect Effects 0.000 description 1
- XWGJFPHUCFXLBL-UHFFFAOYSA-M rongalite Chemical compound [Na+].OCS([O-])=O XWGJFPHUCFXLBL-UHFFFAOYSA-M 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 1
- IZWPGJFSBABFGL-GMFCBQQYSA-M sodium;2-[methyl-[(z)-octadec-9-enoyl]amino]ethanesulfonate Chemical compound [Na+].CCCCCCCC\C=C/CCCCCCCC(=O)N(C)CCS([O-])(=O)=O IZWPGJFSBABFGL-GMFCBQQYSA-M 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
- D01F6/78—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from copolycondensation products
- D01F6/84—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from copolycondensation products from copolyesters
-
- D—TEXTILES; PAPER
- D03—WEAVING
- D03D—WOVEN FABRICS; METHODS OF WEAVING; LOOMS
- D03D15/00—Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used
- D03D15/50—Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used characterised by the properties of the yarns or threads
- D03D15/56—Woven fabrics characterised by the material, structure or properties of the fibres, filaments, yarns, threads or other warp or weft elements used characterised by the properties of the yarns or threads elastic
-
- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04B—KNITTING
- D04B21/00—Warp knitting processes for the production of fabrics or articles not dependent on the use of particular machines; Fabrics or articles defined by such processes
- D04B21/14—Fabrics characterised by the incorporation by knitting, in one or more thread, fleece, or fabric layers, of reinforcing, binding, or decorative threads; Fabrics incorporating small auxiliary elements, e.g. for decorative purposes
- D04B21/18—Fabrics characterised by the incorporation by knitting, in one or more thread, fleece, or fabric layers, of reinforcing, binding, or decorative threads; Fabrics incorporating small auxiliary elements, e.g. for decorative purposes incorporating elastic threads
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06Q—DECORATING TEXTILES
- D06Q1/00—Decorating textiles
- D06Q1/02—Producing patterns by locally destroying or modifying the fibres of a web by chemical actions, e.g. making translucent
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P5/00—Other features in dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form
- D06P5/001—Special chemical aspects of printing textile materials
-
- D—TEXTILES; PAPER
- D10—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B2331/00—Fibres made from polymers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polycondensation products
- D10B2331/04—Fibres made from polymers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polycondensation products polyesters, e.g. polyethylene terephthalate [PET]
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
- Woven Fabrics (AREA)
- Artificial Filaments (AREA)
- Decoration Of Textiles (AREA)
- Knitting Of Fabric (AREA)
Description
本発明は、抜蝕性の高い改質ポリエステル繊維を含む抜蝕加工織編物とその製造方法に関する。 The present invention relates to a erosion-treated woven or knitted fabric comprising a highly removable polyester fiber and a method for producing the same.
従来、抜蝕性の高い繊維と抜蝕し難い繊維の2種以上の繊維からなる織編物に抜蝕糊を柄状に印捺し、抜蝕性の高い繊維を脆化除去する抜蝕加工はオパール加工ともいわれ、広く知られている。抜蝕加工における化学反応は、繊維の種類によって様々である。例えば、ポリエステル繊維を除去する方法はアルカリ減量とも称されており、水酸化ナトリウムや水酸化カリウムなどを用いるアルカリ加水分解である。一方、綿やアセテート等などのセルロース系繊維の除去には、酸加水分解及び炭化や熱有機溶媒による溶解などが利用される。 In the past, in a woven and knitted fabric consisting of two or more fibers of highly removable fibers and fibers that are difficult to be ejected, an erosion paste is printed in the form of a handle, and removal processing is performed to embrittle the highly removable fibers. Also known as opal processing, it is widely known. The chemical reaction in the erosion process varies depending on the type of fiber. For example, a method of removing polyester fibers is also called alkali reduction, and is alkaline hydrolysis using sodium hydroxide or potassium hydroxide. On the other hand, acid hydrolysis and carbonization, dissolution with a thermal organic solvent, and the like are used to remove cellulosic fibers such as cotton and acetate.
[従来の技術]
抜蝕加工として、抜蝕性の高い変性ポリエステル繊維と抜蝕性の低い未変性ポリエステル繊維からなる織編物に対して抜蝕糊を柄状に印捺し、抜蝕性の高い変性ポリエステル繊維を除去することは公知であり、抜蝕加工剤としては水酸化ナトリウムや水酸化カリウムを含む糊液を印捺し熱処理する方法が知られている。
[Prior art]
As a removal process, a removal paste is printed as a pattern on a woven or knitted fabric composed of a highly removable polyester fiber and a low removable polyester fiber, and the highly modified polyester fiber is removed It is well-known that a method of printing and heat-treating a paste solution containing sodium hydroxide or potassium hydroxide as a scraping agent is known.
しかし、抜蝕性の高い変性ポリエステル繊維と抜蝕性の低い未変性ポリエステル繊維の加水分解性の差を利用して抜蝕加工する際に用いる、水酸化ナトリウムや水酸化カリウムによる方法は、未変性ポリエステル繊維まで脆化させかねず、強度低下や抜蝕不良を起こす問題がある。また、水酸化ナトリウムや水酸化カリウムは強アルカリ性物質であるため、人への毒性や刺激性が高く、水性環境への影響も高いという問題点があった。 However, the method using sodium hydroxide or potassium hydroxide, which is used in the extraction process utilizing the difference between the hydrolyzability of the highly removable polyester fiber and the lowly extracted unmodified polyester fiber, has not been used. Even a modified polyester fiber may be embrittled, and there is a problem that the strength is lowered and the poor corrosion is caused. In addition, sodium hydroxide and potassium hydroxide are strongly alkaline substances, so they are highly toxic and irritating to humans, and have a high impact on the aqueous environment.
特許文献1(特開2000−096439号公報)によれば、布帛が変性ポリエステル繊維と未変性ポリエステル繊維とからなる織編物に対する変性ポリエステル繊維の抜蝕加工において、炭酸グアニジンを含む抜蝕加工剤を使った抜蝕加工が提案されている。しかしながら、炭酸グアニジンによる抜蝕加工では変性ポリエステルの抜蝕性は良好だが、未変性ポリエステルが脆化し、強度低下を起こす問題がある。 According to Patent Document 1 (Japanese Patent Application Laid-Open No. 2000-096439), in a process of removing a modified polyester fiber from a woven or knitted fabric in which the fabric comprises a modified polyester fiber and an unmodified polyester fiber, It has been proposed to use a carious process. However, although the removal property of the modified polyester is good in the removal processing with guanidine carbonate, there is a problem that the non-modified polyester is embrittled and strength is reduced.
特許文献2(特開2000−282377号公報)には、布帛が常圧カチオン可染型ポリエステル繊維を必須成分とする織編物に対する変性ポリエステル繊維の抜蝕加工にあって、第4級アンモニウム塩を含む糊液を印捺し、熱処理後にアルカリ減量を行い、変性ポリエステル繊維を除去する方法が提案されている。しかしながら、水酸化ナトリウムを使用したアルカリ減量加工であるため、変性ポリエステル繊維及び未変性ポリエステル繊維の強度が保てないといった問題がある。 Patent Document 2 (Japanese Patent Application Laid-Open No. 2000-282377) discloses a quaternary ammonium salt for removing a modified polyester fiber from a woven or knitted fabric having a normal pressure cationic dyeable polyester fiber as an essential component. A method has been proposed in which the paste solution containing the ink is printed and heat treatment is followed by alkali reduction to remove the modified polyester fiber. However, there is a problem that the strength of the modified polyester fiber and the non-modified polyester fiber can not be maintained since alkali reduction processing using sodium hydroxide is performed.
特許文献3(特開2008−038332号公報)には、布帛が変性ポリエステル繊維と未変性ポリエステル繊維からなる織編物に対する変性ポリエステル繊維の抜蝕加工に当たって、インクジェット捺染により炭酸グアニジン、苛性ソーダ、苛性カリの少なくとも1つを含む抜蝕加工剤を付着させて抜蝕加工を行うことが提案されている。インクジェット捺染によって抜蝕加工剤の付着量をコントロールして抜蝕加工が行われているが、未変性ポリエステル繊維の強度を保持するため、未変性ポリエステル繊維の繊度を太くするか、または、芯部が未変性ポリエステル繊維、鞘部が変性ポリエステル繊維の複合糸を使用して、変性ポリエステル繊維のみに抜蝕加工剤を付着させるなどしているが、いずれにしても未変性ポリエステル繊維に対する脆化は防止できないとの問題がある。 Patent Document 3 (Japanese Patent Laid-Open No. 2008-038332) discloses at least guanidine carbonate, caustic soda and caustic potash by ink jet printing in the process of removing modified polyester fibers from a woven or knitted fabric in which the fabric comprises modified polyester fibers and unmodified polyester fibers. It has been proposed to carry out the erosion process by depositing one of the scraping agents. Although the removal processing is performed by controlling the adhesion amount of the removal processing agent by ink jet printing, in order to maintain the strength of the unmodified polyester fiber, the fineness of the unmodified polyester fiber is increased or the core portion Although a composite yarn of unmodified polyester fiber and modified polyester fiber in the sheath part is used to attach the erosion-finishing agent only to the modified polyester fiber, in any case, the embrittlement of the unmodified polyester fiber is There is a problem that it can not prevent.
特許文献4(国際公開第2007/086593号パンフレット)には、抜蝕加工を施す布帛は非弾性繊維と弾性繊維とから構成され、非弾性繊維には抜蝕性繊維であるカチオン可染ポリエステル繊維と非抜蝕性繊維であるナイロン繊維とが使われ、弾性繊維にエーテル系ポリウレタン繊維が使われており、抜蝕加工剤には水酸化ナトリウムが使用されているため、抜蝕の対象外であるカチオン可染ポリエステル繊維やポリウレタン繊維が抜蝕されてしまい、強度低下を起こす問題がある。 According to Patent Document 4 (WO 2007/086593), a fabric to be subjected to a removal process is composed of an inelastic fiber and an elastic fiber, and a non-elastic fiber is a cationic dyeable polyester fiber which is an extractable fiber. And nylon fiber, which is non-erodible fiber, and ether polyurethane fiber is used as elastic fiber, and sodium hydroxide is used as a decoloring agent. Some cationic dyed polyester fibers and polyurethane fibers are removed and there is a problem that the strength is reduced.
上記のとおり、変性ポリエステル繊維を抜蝕する抜蝕加工において、強アルカリでないと十分な抜蝕がなされず、強アルカリを使うと抜蝕加工した布帛の強度が低下する問題がある。この状況に鑑みて本発明は、十分な抜蝕性能を有する改質ポリエステル繊維を用い、弱アルカリでも抜蝕ができ易くし、未改質ポリエステル繊維を含む抜蝕部以外の繊維の強度低下が避けられる抜蝕性の高い抜蝕加工織編物を提供することを課題としている。 As described above, in the removal process for removing modified polyester fibers, sufficient removal is not performed unless it is a strong alkali, and when a strong alkali is used, there is a problem that the strength of the removed fabric decreases. In view of this situation, the present invention uses a modified polyester fiber having sufficient removal performance, makes it easy to perform removal even with weak alkali, and reduces the strength of fibers other than the removed part including unmodified polyester fiber. It is an object of the present invention to provide a highly removable dental erosion-processed woven or knitted fabric which can be avoided.
従来技術では、変性ポリエステル繊維と未変性ポリエステル繊維の織編物の抜蝕加工において、未変性ポリエステル繊維の脆化を防止するために、抜蝕糊に水酸化ナトリウムや水酸化カリウムなどの強アルカリ性物質を使用せず、アルカリ減量促進剤を印捺熱処理し、印捺熱処理後のアルカリ減量時に印捺部のアルカリ減量を促進させることが検討されていた。しかしながら発明者らは、変性ポリエステル繊維の更なる改質に着目し、改質されたポリエステル繊維が水酸化ナトリウムや水酸化カリウムなどの強アルカリ性物質を使用せず、未改質ポリエステル繊維やポリウレタン繊維に強度低下の影響を与えずに、改質ポリエステル繊維のみを特定のpH領域でアルカリ減量が行えることを見出した。 In the prior art, in order to prevent the embrittlement of unmodified polyester fibers in the process of removing the woven or knitted fabric of modified polyester fibers and unmodified polyester fibers, strongly alkaline substances such as sodium hydroxide and potassium hydroxide are used as the paste to be removed. It has been studied to heat-treat the alkali weight loss promoter without using it and to promote alkali weight loss in the printing area at the time of alkali weight reduction after the heat treatment. However, the inventors focused on further modification of the modified polyester fiber, and the modified polyester fiber does not use a strongly alkaline substance such as sodium hydroxide or potassium hydroxide, and unmodified polyester fiber or polyurethane fiber It has been found that alkali reduction can be performed only at a specific pH range of the modified polyester fiber without the influence of strength reduction.
本発明の織編物は、pH8以上13以下の条件下において減量する改質ポリエステル繊維と非減量繊維とを含有する織編物であって、前記改質ポリエステル繊維が減量された抜蝕部分を有する織編物である。 The woven or knitted fabric according to the present invention is a woven or knitted fabric containing modified polyester fiber and non-weight-loss fiber which loses weight under the condition of pH 8 to 13, and which has a removed portion from which the modified polyester fiber is lost. It is a knitted fabric.
本発明の織編物は、抜蝕部分の織編物の破裂強度が250kPa以上900kPa以下であることが好ましい。
本発明の織編物は、織編物の非抜蝕部分の破裂強度に対する織編物の抜蝕部分の破裂強度の強度保持率の50%以上であることが好ましい。
In the woven or knitted fabric of the present invention, the burst strength of the woven or knitted fabric at the removed portion is preferably 250 kPa or more and 900 kPa or less.
The woven or knitted fabric of the present invention preferably has a strength retention of 50% or more of the burst strength of the ejected portion of the woven or knitted fabric relative to the burst strength of the non-extracted portion of the woven or knitted fabric.
本発明の織編物は、前記改質ポリエステル繊維が、エチレンテレフタレートを主たる構成単位とし、炭素数4以上8以下の脂肪族ジカルボン酸16モル%以上25モル%以下、及び金属スルホネート基含有芳香族ジカルボン酸2モル%以上5モル%以下が共重合された改質ポリエステルであることが好ましい。 In the woven or knitted fabric according to the present invention, the modified polyester fiber contains ethylene terephthalate as a main constituent unit, 16 mol% to 25 mol% of aliphatic dicarboxylic acid having 4 to 8 carbon atoms, and metal sulfonate group-containing aromatic dicarboxylic acid It is preferable that it is a modified polyester in which 2 to 5 mol% of acid is copolymerized.
本発明の織編物は、前記非減量繊維が、合成繊維を50質量%以上95質量%以下含有することが好ましい。
本発明の織編物は、前記合成繊維が、レギュラーポリエステル繊維、ポリアミド繊維、弾性繊維、ポリオレフィン繊維、アクリル繊維のいずれかであることが好ましい。
In the woven or knitted fabric of the present invention, the non-weight loss fiber preferably contains 50% by mass or more and 95% by mass or less of the synthetic fiber.
In the woven or knitted fabric of the present invention, the synthetic fiber is preferably any one of regular polyester fiber, polyamide fiber, elastic fiber, polyolefin fiber and acrylic fiber.
本発明の織編物は、前記改質ポリエステル繊維の単繊維繊度が0.6dtex以上3.5dtex以下であることが好ましい。
本発明の織編物は、前記弾性繊維が、ポリウレタン繊維、ポリトリメチレンテレフタレート繊維、ポリブチレンテレフタレート繊維のいずれかからなることが好ましい。
In the woven or knitted fabric of the present invention, the single fiber fineness of the modified polyester fiber is preferably 0.6 dtex or more and 3.5 dtex or less.
In the woven or knitted fabric according to the present invention, the elastic fiber is preferably made of any of polyurethane fiber, polytrimethylene terephthalate fiber, and polybutylene terephthalate fiber.
本発明の織編物の製造方法は、pH8以上13以下の条件下において減量する改質ポリエステル繊維と非減量繊維とを含有する生地に、抜蝕加工剤を印捺し、抜蝕加工剤を印捺した部分に過熱蒸気を付与して減量加工する織編物の製造方法であって、前記抜蝕加工剤のpHが8以上13以下であり、加熱方法は、150℃以上200℃以下の過熱蒸気であり、加熱時間が5分以上15分以下である織編物の製造方法である。 In the method for producing a woven or knitted fabric according to the present invention, a fabric having a modified polyester fiber and a non-weight-reduced fiber whose weight is reduced under the condition of pH 8 to 13 is printed with a discoloring agent and printed with a discoloring agent. The method of producing a woven or knitted fabric in which the superheated steam is applied to the portion to reduce the weight and the pH of the scraping agent is 8 or more and 13 or less, and the heating method is a superheated steam of 150 ° C. or more and 200 ° C. or less It is a method of manufacturing a woven or knitted fabric which has a heating time of 5 minutes to 15 minutes.
本発明によれば、改質ポリエステル繊維を含む織編物の抜蝕加工において、改質ポリエステル繊維の抜蝕部以外の強度低下が起こらず、かつ、改質ポリエステル繊維以外の繊維を含む織編物の抜蝕部の強度低下を起こさないことが可能であり、同時に良好な抜蝕作用を得ることができる。本発明によれば、改質ポリエステル繊維が良好に抜蝕され強度低下の無い抜蝕加工品を得ることができる。 According to the present invention, in the process of removing the woven or knitted fabric containing the modified polyester fiber, the strength of the modified polyester fiber other than the removed portion does not decrease, and the woven or knitted fabric containing the fiber other than the modified polyester fiber It is possible not to cause the strength reduction of the removed portion, and at the same time, it is possible to obtain a good removal effect. According to the present invention, it is possible to obtain a scraped product having good strength without corrosion of the modified polyester fiber.
本発明の織編物は、pH8以上13以下の条件下において減量する改質ポリエステル繊維と非減量繊維とを含有する織編物であって、前記改質ポリエステル繊維が、エチレンテレフタレートを主たる構成単位とし、炭素数4以上8以下の脂肪族ジカルボン酸16モル%以上25モル%以下、及び金属スルホネート基含有芳香族ジカルボン酸2モル%以上5モル%以下が共重合された改質ポリエステル繊維であり、前記改質ポリエステル繊維が減量された抜蝕部分を有する織編物である。 The woven or knitted fabric according to the present invention is a woven or knitted fabric containing a modified polyester fiber which loses weight under conditions of pH 8 to 13 and a non-weight loss fiber, and the modified polyester fiber has ethylene terephthalate as a main constituent unit, A modified polyester fiber in which 16 to 25 mol% of aliphatic dicarboxylic acid having 4 to 8 carbon atoms and 2 to 5 mol% of metal sulfonate group-containing aromatic dicarboxylic acid are copolymerized, It is a woven or knitted fabric having a removed portion from which a modified polyester fiber is reduced.
本発明の織編物は、pHが8以上であれば、前記改質ポリエステルが減量でき易くなり、pHが13以下であれば、非減量繊維の脆化を低減することができる。前記pHは、前記抜触性の観点からpH9以上12.5以下がより好ましく、pH10以上12以下がさらに好ましい。 In the woven or knitted fabric of the present invention, if the pH is 8 or more, the amount of the modified polyester can be easily decreased, and if the pH is 13 or less, the embrittlement of non-weight loss fibers can be reduced. The pH is more preferably 9 or more and 12.5 or less, and still more preferably 10 or more and 12 or less from the viewpoint of the removal property.
本発明の織編物は、抜蝕部分の織編物の破裂強度が250kPa以上900kPa以下であることが好ましい。
前記破裂強度が250kPa以上であれば、製品としての使用上問題ない強度である。また、900kPaあれば使用上十分な強度である。
前記観点から、前記破裂強度は、400kPa以上が好ましく、600kPa以上がさらに好ましい。
In the woven or knitted fabric of the present invention, the burst strength of the woven or knitted fabric at the removed portion is preferably 250 kPa or more and 900 kPa or less.
If the said burst strength is 250 kPa or more, it is a strength which does not have a problem in use as a product. In addition, 900 kPa is sufficient strength for use.
From the above viewpoint, the rupture strength is preferably 400 kPa or more, and more preferably 600 kPa or more.
本発明の織編物は、織編物の非抜蝕部分の破裂強度に対する織編物の抜蝕部分の破裂強度の強度保持率が50%以上であることが好ましい。
前記破裂強度の強度保持率が50%以上であれば、抜蝕部分に応力が集中し過ぎて織編物が破断することが低減される。
前記観点から前記強度保持率は、70%以上がより好ましく、85%以上がさらに好ましい。
The woven or knitted fabric of the present invention preferably has a strength retention rate of 50% or more of the burst strength of the ejected portion of the woven or knitted fabric relative to the burst strength of the non-extracted portion of the woven or knitted fabric.
When the strength retention rate of the burst strength is 50% or more, it is possible to reduce the breakage of the woven or knitted fabric due to excessive concentration of stress on the portion to be removed.
From the viewpoint, the strength retention rate is more preferably 70% or more, and still more preferably 85% or more.
前記改質ポリエステル繊維は、炭素数4以上8以下の脂肪族ジカルボン酸の共重合量が16モル%以上であれば、pH8以上13以下の範囲でも減量され易くなり、25モル%以下であれば、該繊維の紡糸時の糸切れが低減でき、生産性が良好となる。
前記観点から、前記炭素数4以上8以下の脂肪族ジカルボン酸の共重合量は、20モル%以下であることがより好ましい。
The modified polyester fiber, if copolymerization amount of the aliphatic dicarboxylic acid having 4 to 8 carbon atoms is 16 mol% or more, likely to be reduced in the range of pH 8 to 13, there in 25 mol% or less For example, yarn breakage during spinning of the fiber can be reduced, and the productivity is improved.
From the above viewpoint, the copolymerization amount of the aliphatic dicarboxylic acid having 4 to 8 carbon atoms is more preferably 20 mol% or less.
本発明の織編物は、非減量繊維が、合成繊維を50質量%以上95質量%以下含有することが好ましい。
織編物に対する前記合成繊維の含有量が50質量%以上であれば、抜蝕部分の破裂強度の低下が少なくできる。また、前記合成繊維の含有量が95質量%以下であれば、抜蝕繊維を含むことができ、抜蝕加工の効果を出しやすくできる。前記観点から、前記合成繊維の含有量は、60質量%以上80質量%以下がより好ましい。
In the woven or knitted fabric of the present invention, the non-weight loss fibers preferably contain 50% by mass or more and 95% by mass or less of synthetic fibers.
When the content of the synthetic fiber with respect to the woven or knitted fabric is 50% by mass or more, the decrease in the burst strength of the scraped portion can be reduced. Moreover, if content of the said synthetic fiber is 95 mass% or less, it can contain a caries fiber, and it can be easy to take out the effect of caries processing. From the viewpoint, the content of the synthetic fiber is more preferably 60% by mass to 80% by mass.
本発明の織編物は、前記合成繊維が、レギュラーポリエステル繊維、ポリアミド繊維、弾性繊維、ポリオレフィン繊維、アクリル繊維のいずれかの繊維であることが好ましい。
中でも、強度の点でレギュラーポリエステル繊維が好ましく、ストレッチ性を出す観点からは弾性繊維であることが好ましい。
In the woven or knitted fabric of the present invention, the synthetic fiber is preferably any one of regular polyester fiber, polyamide fiber, elastic fiber, polyolefin fiber and acrylic fiber.
Among them, regular polyester fibers are preferable in terms of strength, and elastic fibers are preferable in terms of achieving stretchability.
本発明の織編物は、前記改質ポリエステル繊維の単繊維繊度が0.6dtex以上3.5dtex以下であることが好ましい。
前記単繊維繊度が0.6dtex以上であれば、織編物の強度を高めることができ、3.5dtex以下であれば、抜蝕性が良好となり、織編物の風合いもソフトにでき易くなる。
前記観点から、前記単繊維繊度が0.9dtex以上2.5dtex以下であることがより好ましい。
In the woven or knitted fabric of the present invention, the single fiber fineness of the modified polyester fiber is preferably 0.6 dtex or more and 3.5 dtex or less.
If the single fiber fineness is 0.6 dtex or more, the strength of the woven or knitted fabric can be enhanced, and if it is 3.5 dtex or smaller, the peelability becomes good and the texture of the woven or knitted fabric can be softened easily.
From the above viewpoint, the single fiber fineness is more preferably 0.9 dtex or more and 2.5 dtex or less.
本発明の織編物は、前記弾性繊維が、既述したとおりポリウレタン繊維、ポリトリメチレンテレフタレート繊維、ポリブチレンテレフタレート繊維のいずれかであることが好ましい。 In the woven or knitted fabric according to the present invention, it is preferable that the elastic fiber is any one of polyurethane fiber, polytrimethylene terephthalate fiber and polybutylene terephthalate fiber as described above.
本発明の織編物は、改質ポリエステル繊維、レギュラーポリエステル繊維及びポリウレタン繊維からなることが好ましい。前記構成であれば、ストレッチ性を有し、強度が高く、ソフトな風合いの織編物を得ることができる。 The woven or knitted fabric of the present invention preferably comprises modified polyester fibers, regular polyester fibers and polyurethane fibers. With the above configuration, it is possible to obtain a woven or knitted fabric having stretchability, high strength and soft texture.
本発明の織編物の製造方法は、pH8以上13以下の条件下において減量する、エチレンテレフタレートを主たる構成単位とし、炭素数4以上8以下の脂肪族ジカルボン酸16モル%以上25モル%以下、及び金属スルホネート基含有芳香族ジカルボン酸2モル%以上5モル%以下が共重合された改質ポリエステル繊維と非減量繊維とを含有する生地に、抜蝕加工剤を印捺し、抜蝕加工剤を印捺した部分に過熱蒸気を与えて減量加工する織編物の製造方法であって、前記抜蝕加工剤のpHが8以上13以下であり、加熱方法は、150℃以上200℃以下の過熱蒸気であり、加熱時間が5分以上15分以下である。 The method for producing a woven or knitted fabric according to the present invention comprises ethylene terephthalate as a main constituent unit and reduces 16 to 25 mol% of an aliphatic dicarboxylic acid having 4 to 8 carbon atoms , which decreases in weight under pH 8 to 13 conditions. A scraping agent is printed on a fabric containing a modified polyester fiber copolymerized with 2 mol% to 5 mol% of a metal sulfonate group-containing aromatic dicarboxylic acid and a non-weight loss fiber, and the scraping agent is printed A method for producing a woven or knitted fabric in which overheated steam is given to a roasted portion to reduce weight, wherein the pH of the scraping agent is 8 or more and 13 or less, and the heating method is overheated steam of 150 ° C. or more and 200 ° C. or less The heating time is 5 minutes or more and 15 minutes or less.
前記加熱方法は、抜蝕加工剤を印捺した部分に150℃以上200℃以下の過熱蒸気を与える。前記過熱蒸気の温度が150℃以上になると、抜蝕性が良好となり、200℃以下であれば、ポリエステル系繊維の風合いが硬くなることを低減できる。 The said heating method gives the superheated steam of 150 degreeC or more and 200 degrees C or less to the part which printed the erosion processing agent. When the temperature of the superheated steam is 150 ° C. or more, the removal property is good, and when the temperature is 200 ° C. or less, the texture of the polyester fiber can be reduced to be hard.
前記加熱時間は、5分以上15分以下であることが好ましい。
前記加熱時間が、5分以上であれば、抜蝕性が良好となり、15分以下であれば、非抜蝕部分の強度低下が少なくできる。
The heating time is preferably 5 minutes or more and 15 minutes or less.
If the heating time is 5 minutes or more, the carriability will be good, and if it is 15 minutes or less, the strength reduction of the non-eroded portion can be reduced.
抜蝕加工剤は、糊剤と、炭酸グアニジンを除く特定のpH領域(pH9以上13以下) で抜蝕作用を有する成分とを含むことを特徴とする。抜蝕作用を有する前記成分としては、炭酸ナトリウムまたは炭酸カリウムの1種または2種が好ましく、炭酸ナトリウムの1種がより好ましい。炭酸ナトリウムまたは炭酸カリウムの使用量は抜蝕する改質ポリエステル繊維の質量に応じて調整すれはよいが、一般的には抜蝕加工剤に対して5質量%以上15質量%以下の範囲で用いることが好ましい。抜蝕加工剤には、必要に応じて抜蝕促進剤を含んでいても良い。抜蝕促進剤は、特に限定されるものではなく、市販されているものを使用することができる。例えば、明成化学工業株式会社製、メイプリンターOP−2が好ましい。 The scraping agent is characterized by containing a sizing agent and a component having a scraping action at a specific pH range (pH 9 or more and 13 or less) excluding guanidine carbonate. As said component which has a removing effect, 1 type or 2 types of sodium carbonate or potassium carbonate are preferable, and 1 type of sodium carbonate is more preferable. The use amount of sodium carbonate or potassium carbonate may be adjusted according to the mass of the modified polyester fiber to be removed, but generally, it is used in the range of 5% by mass to 15% by mass with respect to the removal processing agent Is preferred. The disintegration processing agent may contain a disintegration promoter as needed. There is no particular limitation on the dental caries accelerator, and commercially available ones can be used. For example, Meisei Chemical Co., Ltd. make, May printer OP-2 is preferable.
抜蝕加工剤に含まれる糊剤としては、ローカストビーンガム系、デンプン系、デキストリン系、クリスタルガム系、トラガントガム系、セルロース系、カルボキシメチルセルロース、ポリビニルアルコール、ポリアクリル酸ソーダなどの、天然、加工、半合成、合成の糊剤を単独でまたは2種以上を用いることができる。糊剤の割合は、抜蝕加工剤を印捺し、熱処理を行うために適切な粘度を保持できる限り特に制限されないが、例えば抜蝕加工剤に対して1質量%以上10質量%以下含有されることが好ましい。
抜蝕加工剤には、さらに、染料など他の化合物を配合することもできる。
As the sizing agent contained in the caries finishing agent, natural, processed, such as locust bean gum type, starch type, dextrin type, crystal gum type, tragant gum type, cellulose type, carboxymethyl cellulose, polyvinyl alcohol, sodium polyacrylate, etc. Semi-synthetic and synthetic pastes may be used alone or in combination of two or more. The proportion of the sizing agent is not particularly limited as long as an appropriate viscosity can be maintained to print the scraping agent and carry out heat treatment, but it is contained, for example, at 1% by mass to 10% by mass with respect to the scraping agent Is preferred.
In addition, other compounds such as a dye can also be added to the scraping agent.
上記の抜蝕加工剤を用いる抜蝕加工方法について説明する。
上記抜蝕加工剤は、改質ポリエステル繊維を含む織編物に対して好ましく適用される。
改質ポリエステル繊維と組み合わせて用いる繊維は、改質ポリエステル繊維と異なる非減量性を有する繊維であれば特に制限されないが、例えば未変性ポリエステル繊維(未改質のポリエチレンテレフタレートからなり、レギュラーポリエステル繊維ともいわれる。)、ポリアミド繊維、ポリトリメチレンテレフタレート繊維、ポリブチレンテレフタレート繊維、ポリプロピレン繊維、ポリエチレン繊維、ポリウレタン繊維などを用いることができる。改質ポリエステル繊維とこれらの繊維とを、混紡、混繊、交撚等の任意の方法で組み合わせた糸条、ステープル糸条などからなる織編物について、抜蝕加工を行う。上記織編物は、必要に応じて染色を行った布帛を使用してもよい。染色としては公知の任意の方法にて布帛の全部または一部を無地染めまたは捺染により行う。
Description will be made of a method of removing by using the above-described removing agent.
The above-mentioned scraping agent is preferably applied to a woven or knitted fabric containing a modified polyester fiber.
The fiber used in combination with the modified polyester fiber is not particularly limited as long as it is a fiber having a non-weight reducing property different from that of the modified polyester fiber, for example, unmodified polyester fiber (consisting of unmodified polyethylene terephthalate, regular polyester fiber Polyamide fiber, polytrimethylene terephthalate fiber, polybutylene terephthalate fiber, polypropylene fiber, polyethylene fiber, polyurethane fiber and the like can be used. A discharge process is performed on a woven or knitted fabric composed of yarns, staple yarns and the like in which the modified polyester fibers and these fibers are combined by any method such as blending, mixing, and twisting. The woven and knitted fabric may use a dyed fabric as required. For dyeing, all or part of the fabric is dyed or printed by any known method.
抜蝕加工は既述した抜蝕加工剤を用いて、概略的には印捺、熱処理、洗浄という公知の工程に従って行うことができる。印捺工程において、改質ポリエステル繊維を含む織編物に、抜蝕加工剤を所望の模様に応じた形状で印捺する。抜蝕加工剤の印捺には、捺染法、スプレイ法などが用いられる。捺染法としては特に限定されず、型枠捺染法、フラットスクリーン法、ロータリースクリーン法、ローラー法などが用いられる。織編物への抜蝕加工剤の付着量は、印捺の方法、布帛の織編組織、所望の模様により任意に決定することができる。 The removal process can be carried out using the above-described removal process agent in accordance with generally known steps of printing, heat treatment and cleaning. In the printing step, the scraping agent is printed in a shape according to the desired pattern on the woven or knitted fabric containing the modified polyester fiber. A printing method, a spray method, etc. are used for the printing of the scraping agent. The printing method is not particularly limited, and a mold printing method, a flat screen method, a rotary screen method, a roller method and the like are used. The adhesion amount of the removing agent to the woven or knitted fabric can be optionally determined according to the method of printing, the woven / knitted structure of the fabric, and the desired pattern.
例えば、フラットスクリーン法の場合、印捺を行う織編組織、所望の模様を印捺する型枠のメッシュなどにより、抜蝕加工剤の粘度、ゴムスキージの硬度、抜蝕加工剤の印捺を行うゴムスキージ圧力、スキージの印捺スピードを決定し、布帛へ抜蝕加工剤を所望の模様で均一に付与する。布帛へ均一に付着しているかの確認としては、目視で印捺部のカスレがないか、ゴムスキージ左右での模様に差がないか、印捺部の裏面へ抜蝕加工剤が均一に浸透しているかなどを確認することにより行う。また、抜蝕加工剤の付着部以外の部分に抜蝕加工剤を含まない染色糊により所望の模様に応じた形状を印捺してもよい。染色糊の捺染法は特に限定されず、抜蝕加工剤と同様に印捺を行う。抜蝕加工剤や染色糊を織編物に印捺した後、適宜乾燥し、続いて熱処理を行う。 For example, in the case of the flat screen method, the viscosity of a scraping agent, the hardness of a rubber squeegee, and printing of a scraping agent is performed by a woven or knitted structure to be imprinted, or a mesh of a formwork to print a desired pattern. The rubber squeegee pressure, the squeegee printing speed are determined, and the fabric is uniformly applied with a scraping agent in a desired pattern. As confirmation of whether it adheres uniformly to the fabric, there is no blurring of the printing part visually, there is no difference in the pattern on the left and right of the rubber squeegee, or the scraping agent uniformly penetrates the back of the printing part. It does by confirming whether it is. Moreover, you may print the shape according to a desired pattern with the dyeing paste which does not contain a erosion processing agent in parts other than the adhesion part of a erosion processing agent. The printing method of the dyeing paste is not particularly limited, and printing is performed in the same manner as the removal processing agent. After printing a scraping agent and a dyeing paste on a woven or knitted fabric, it is suitably dried and then heat-treated.
熱処理方法としては、ベーキング法、スチーム法、HTスチーム法などが挙げられ、HTスチーム法がより好ましい。 As the heat treatment method, a baking method, a steam method, an HT steam method and the like can be mentioned, and the HT steam method is more preferable.
熱処理工程の後、印捺部の脆化した改質ポリエステル繊維の除去、抜蝕加工剤に併用した染料の繊維への未固着染料の除去、抜蝕加工剤の付着部以外に使用した染色糊の糊剤、繊維への未固着染料などの洗浄を行う。洗浄方法としては特に限定されず公知の工程により洗浄を行う。例えば、界面活性剤2g/Lでの洗浄、界面活性剤2g/L,ソーダ灰2g/Lでのアルカリ洗浄、界面活性剤2g/L,酢酸(90%)2g/Lでの酸性洗浄、界面活性剤2g/L,ソーダ灰2g/L,ハイドロサルファイトまたは二酸化チオ尿素2g/Lでのアルカリ還元洗浄、界面活性剤2g/L,酢酸(90%)2g/L,ロンガリット4g/Lでの酸性還元洗浄がある。洗浄温度は60℃以上100℃以下が好ましく、洗浄時間は5分間以上30分間以下が好ましい。その後、水洗、脱水、乾燥を行う。 After the heat treatment step, removal of the embrittled modified polyester fiber in the printing part, removal of non-fixed dye to the fiber of dye used in combination with the discoloring agent, dyeing paste used other than the adhering part of the discoloring agent And washing of unpasted dye, etc. on fibers. It does not specifically limit as a washing | cleaning method, It wash | cleans by a well-known process. For example, washing with surfactant 2 g / L, alkaline washing with surfactant 2 g / L, soda ash 2 g / L, acidic washing with surfactant 2 g / L, acetic acid (90%) 2 g / L, interface Alkali reduction washing with activator 2 g / L, soda ash 2 g / L, hydrosulfite or thiourea dioxide 2 g / L, surfactant 2 g / L, acetic acid (90%) 2 g / L, Rongalite 4 g / L There is an acid reduction wash. The washing temperature is preferably 60 ° C. or more and 100 ° C. or less, and the washing time is preferably 5 minutes or more and 30 minutes or less. Thereafter, washing with water, dehydration and drying are performed.
洗浄に用いる界面活性剤としては、非イオン界面活性剤、アニオン界面活性剤、カチオン界面活性剤、両性界面活性剤が挙げられ、これらを単独で又は2種以上を混合して用いることができる。 As surfactant used for washing | cleaning, nonionic surfactant, anionic surfactant, cationic surfactant, and amphoteric surfactant are mentioned, These can be used individually or in mixture of 2 or more types.
非イオン界面活性剤としては、高級アルコールアルキレンオキサイド付加物、アルキルフェノールアルキレンオキサイド付加物、スチレン化アルキルフェノールアルキレンオキサイド付加物、スチレン化フェノールアルキレンオキサイド付加物、高級アルキルアミンアルキレンオキサイド付加物などのエーテル型の非イオン界面活性剤;脂肪酸アルキレンオキサイド付加物、多価アルコール脂肪酸エステルアルキレンオキサイド付加物、脂肪酸アミドアルキレンオキサイド付加物、油脂のアルキレンオキサイド付加物などのエーテルエステル型の非イオン界面活性剤;ポリプロピレングリコールエチレンオキサイド付加物などのポリアルキレングリコール型の非イオン界面活性剤;グリセロールの脂肪酸エステル、ペンタエリスリトールの脂肪酸エステル、ソルビトールの脂肪酸エステル、ソルビタンの脂肪酸エステル、ショ糖の脂肪酸エステルなどのエステル型の非イオン界面活性剤;多価アルコールのアルキルエーテル、アルカノールアミン類の脂肪酸アミドなどのその他の非イオン界面活性剤を挙げることができる。アルキレンオキサイドとしては、エチレンオキサイド、プロピレンオキサイド、ブチレンオキサイドを挙げることができ、アルキレンオキサイドの付加形態は、2種以上のランダム付加でも、ブロック付加でもよい。 Nonionic surfactants include non-ether type non-ether surfactants such as higher alcohol alkylene oxide adducts, alkyl phenol alkylene oxide adducts, styrenated alkyl phenol alkylene oxide adducts, styrenated phenol alkylene oxide adducts, higher alkyl amine alkylene oxide adducts and the like Ion surfactants; Ether ester type nonionic surfactants such as fatty acid alkylene oxide adducts, polyhydric alcohol fatty acid ester alkylene oxide adducts, fatty acid amide alkylene oxide adducts, alkylene oxide adducts of fats and oils, etc .; polypropylene glycol ethylene oxide Polyalkylene glycol type nonionic surfactants such as adducts; fatty acid esters of glycerol, fats of pentaerythritol Ester type nonionic surfactants such as acid esters, fatty acid esters of sorbitol, fatty acid esters of sorbitan, fatty acid esters of sucrose; other nonionic surfactants such as alkyl ethers of polyhydric alcohols and fatty acid amides of alkanolamines Agents can be mentioned. Examples of the alkylene oxide include ethylene oxide, propylene oxide and butylene oxide. The addition form of the alkylene oxide may be two or more kinds of random addition or block addition.
アニオン界面活性剤としては、脂肪酸セッケンなどのカルボン酸塩のアニオン界面活性剤;高級アルコール硫酸エステル塩、高級アルコールアルキレンオキサイド付加物硫酸エステル塩、ポリオキシアルキレンエーテル硫酸エステル塩、フェノールアルキレンオキサイド付加物硫酸エステル塩、アルキルフェノールアルキレンオキサイド付加物硫酸エステル塩、スチレン化アルキルフェノールアルキレンオキサイド付加物硫酸エステル塩、スチレン化フェノールアルキレンオキサイド付加物硫酸エステル塩、多価アルコールアルキレンオキサイド付加物硫酸エステル塩、硫酸化油、硫酸化脂肪酸エステル、硫酸化脂肪酸、硫酸化オレフィン等の硫酸エステル塩;アルキルベンゼンスルホン酸塩、アルキルナフタレンスルホン酸塩、ナフタレンスルホン酸等のホルマリン縮合物、α−オレフィンスルホン酸塩、パラフィンスルホン酸塩、スルホコハク酸ジエステル塩などのスルホン酸塩などのスルホン酸エステル塩のアニオン界面活性剤;オレオイルメチルタウリンナトリウム塩、高級アルコールリン酸エステル塩、ポリオキシアルキレンエーテルリン酸エステル塩、フェノールアルキレンオキサイド付加物リン酸エステル塩、アルキルフェノールアルキレンオキサイド付加物リン酸エステル塩、スチレン化アルキルフェノールアルキレンオキサイド付加物リン酸エステル塩、スチレン化フェノールアルキレンオキサイド付加物リン酸エステル塩、多価アルコールアルキレンオキサイド付加物リン酸エステル塩などのリン酸エステル塩;N−メチルタウリンオレイン酸塩、N−メチルタウリンステアリン酸塩などのその他のアニオン界面活性剤が挙げられる。アルキレンオキサイドとしては、エチレンオキサイド、プロピレンオキサイド、ブチレンオキサイドを挙げることができ、アルキレンオキサイドの付加形態は、2種以上のランダム付加でも、ブロック付加でもよい。塩としては、リチウム、ナトリウム、カリウム等のアルカリ金属塩;アンモニア、メチルアミン、エチルアミン、プロピルアミン、ブチルアミン、アリルアミンなどの1級アミン;ジメチルアミン、ジエチルアミン、ジプロピルアミン、ジブチルアミン、ジアリルアミン等の2級アミン;トリメチルアミン、トリエチルアミン、トリプロピルアミン、トリブチルアミン等の3級アミン;モノエタノールアミン、ジエタノールアミン、トリエタノールアミン等のアルカノールアミンなどのアミン塩を挙げることができる。 As anionic surfactant, anionic surfactant of carboxylic acid salt such as fatty acid soap; higher alcohol sulfuric acid ester salt, higher alcohol alkylene oxide adduct sulfuric acid ester salt, polyoxyalkylene ether sulfuric acid ester salt, phenol alkylene oxide adduct sulfuric acid Ester salt, alkylphenol alkylene oxide adduct sulfate ester salt, styrenated alkylphenol alkylene oxide adduct sulfate ester salt, styrenated phenol alkylene oxide adduct sulfate ester salt, polyhydric alcohol alkylene oxide adduct sulfate ester salt, sulfated oil, sulfuric acid Sulfated fatty acid ester, sulfated fatty acid, sulfated ester salt such as sulfated olefin; alkyl benzene sulfonate, alkyl naphthalene sulfonate, naphthalene Anionic surfactants of sulfonic acid ester salts such as formalin condensates such as rufonic acid, α-olefin sulfonates, paraffin sulfonates and sulfonates such as sulfosuccinic acid diester salts; oleoyl methyl taurine sodium salt, higher alcohol Phosphoric acid ester salt, polyoxyalkylene ether phosphoric acid ester salt, phenol alkylene oxide adduct phosphoric acid ester salt, alkylphenol alkylene oxide adduct phosphoric acid ester salt, styrenated alkyl phenol alkylene oxide adduct phosphoric acid ester salt, styrenated phenol alkylene Oxide adduct phosphate ester salt, polyhydric alcohol alkylene oxide adduct phosphate ester salt and other phosphate ester salts; N-methyl taurine oleate, N-methyl ta Other anionic surfactants such as urin stearate are included. Examples of the alkylene oxide include ethylene oxide, propylene oxide and butylene oxide. The addition form of the alkylene oxide may be two or more kinds of random addition or block addition. As salts, alkali metal salts such as lithium, sodium and potassium; primary amines such as ammonia, methylamine, ethylamine, propylamine, butylamine and allylamine; dimethylamine, diethylamine, dipropylamine, dibutylamine and diarylamine 2 Examples include secondary amines; tertiary amines such as trimethylamine, triethylamine, tripropylamine and tributylamine; and amine salts such as alkanolamines such as monoethanolamine, diethanolamine and triethanolamine.
カチオン界面活性剤としては、アルキルエーテル4級アンモニウム塩、アルキルアミド4級アンモニウム塩、ジアルキルエステル4級アンモニウム塩、ジアルキルイミダゾリン4級アンモニウム塩、アルキルアミドアミン、アルキルエーテルアミン、アルキルアミドグアニジン、アルギニン誘導体を挙げることができる。 Examples of cationic surfactants include alkyl ether quaternary ammonium salts, alkyl amide quaternary ammonium salts, dialkyl ester quaternary ammonium salts, dialkyl imidazoline quaternary ammonium salts, alkylamidoamines, alkylether amines, alkylamidoguanidines, and arginine derivatives. be able to.
両性界面活性剤としては、アルキルベタイン型界面活性剤、アミドプロピルベタイン型界面活性剤、イミダゾリニウムベタイン型界面活性剤などを挙げることができる。 Examples of amphoteric surfactants include alkyl betaine surfactants, amidopropyl betaine surfactants, imidazolinium betaine surfactants and the like.
上記加工方法によって、抜蝕加工剤を印捺した部分の改質ポリエステル繊維が脱落した抜蝕加工品を得ることができる。得られた抜蝕加工品は必要に応じて、染色、仕上げなどの公知の処理を行う。 According to the above processing method, it is possible to obtain a scraped product in which the modified polyester fiber of the portion printed with the scraping agent has fallen off. The resulting scraped product is subjected to known processing such as dyeing and finishing as required.
以下、実施例を挙げて本発明についてより具体的に説明するが、本発明はこれらの実施例に制限されるものではない。
(アルカリ減量率)
アルカリ減量を行った処理布の減量率を処理前後の布の質量から、次式により減量率(%)を求めた。
減量率(%)=〔(原布の質量−処理布の質量)/原布の質量〕×100
(破裂強度)
JIS L 1018のミューレン法に準じて測定した。
(破裂強度保持率)
破裂強度保持率=織編物の抜蝕加工後の抜蝕部分の破裂強度/織編物の抜蝕加工後の非抜蝕部分の破裂強度×100(%)
EXAMPLES Hereinafter, the present invention will be more specifically described by way of examples, but the present invention is not limited to these examples.
(Alkali weight loss rate)
From the weight of the cloth before and after the treatment, the weight loss rate (%) was determined by the following equation.
Weight loss rate (%) = [(mass of original fabric-mass of treated fabric) / mass of original fabric] × 100
(Burst strength)
It measured according to the Murren method of JIS L 1018.
(Burst strength retention rate)
Burst strength retention rate = Burst strength of the removed part after removal of the woven or knitted fabric / Burst strength of non-removed part after removal of the woven or woven material × 100 (%)
[実施例1]
被処理布帛:
エチレンテレフタレートを主たる構成単位とし、アジピン酸が16モル%及び5−ナトリウムイソフタル酸2.5モル%が共重合されたポリエステル樹脂からなる、繊度84dtex、48フィラメントの改質ポリエステル繊維を編成し、天竺組織の横編地を作製した。
前記横編地をミニカラー染色機((株)テクサム技研製、多色回転ポット染色試験機)を用いて、炭酸ナトリウム40g/L、前記横編地の質量と炭酸ナトリウム水溶液の質量の比を1:20、前記水溶液温度を100℃×30分間のアルカリ減量加工を行い、水洗、脱水、乾燥し、加工編地を得た。
前記水溶液のpHは11.8であった。
減量率を、表1に示す。
Example 1
Treated cloth:
Knitted with 48 filaments of a modified polyester fiber consisting mainly of ethylene terephthalate and consisting of a polyester resin copolymerized with 16 mol% of adipic acid and 2.5 mol% of 5-sodium isophthalic acid A weft knit of tissue was made.
Using a mini color dyeing machine (multicolor rotary pot dyeing tester manufactured by Texam Giken Co., Ltd.), the weft knitted fabric is made of sodium carbonate 40 g / L, the ratio of the mass of the weft knitted fabric to the mass of the sodium carbonate aqueous solution The aqueous solution was subjected to alkali weight reduction processing at 100 ° C. for 30 minutes, washed with water, dehydrated and dried to obtain a processed knitted fabric.
The pH of the aqueous solution was 11.8.
The weight loss rates are shown in Table 1.
[比較例1]
横編地に使用した糸を、エチレンテレフタレートを主たる構成単位とし、アジピン酸が5モル%及び5−ナトリウムイソフタル酸2.3モル%が共重合されたポリエステル樹脂からなる、繊度84dtex、48フィラメントのカチオン可染ポリエステル繊維を使用した以外は、実施例1と同様にして加工編地を得た。
表1に、減量率を示す。実施例1と比較して、1/3の減量率であった。
Comparative Example 1
The yarn used for the weft knitted fabric is composed of a polyester resin comprising ethylene terephthalate as the main constituent unit, and containing 5 mol% of adipic acid and 2.3 mol% of 5-sodiumisophthalic acid, having a fineness of 84 dtex and 48 filaments A processed knitted fabric was obtained in the same manner as in Example 1 except that cationic dyed polyester fibers were used.
Table 1 shows the weight loss rate. Compared to Example 1, the weight loss rate was 1/3.
[比較例2]
横編地に使用した糸を、ポリエチレンテレフタレート繊維(未改質のポリエチレンテレフタレートからなるもの。以下、「レギュラーポリエステル繊維」ともいう。)(帝人(株)社製)で構成し、繊度84dtex、36フィラメントを使用した以外は、実施例1と同様にして加工編地を得た。
表1に、減量率を示す。比較例2の編地の減量率は0%であった。
Comparative Example 2
The yarn used for the weft knitted fabric is composed of polyethylene terephthalate fiber (consisting of unmodified polyethylene terephthalate, hereinafter also referred to as "regular polyester fiber") (manufactured by Teijin Ltd.), denier 84 dtex, 36 A processed knitted fabric was obtained in the same manner as in Example 1 except that a filament was used.
Table 1 shows the weight loss rate. The weight loss rate of the knitted fabric of Comparative Example 2 was 0%.
[実施例2]
被処理布帛:
実施例1で作成した横編地を使用し、ミニカラー染色機((株)テクサム技研製、多色回転ポット染色試験機)を用いて、炭酸カリウム40g/L、前記横編地の質量と炭酸ナトリウム水溶液の質量との比を1:20、前記水溶液温度100℃で30分間のアルカリ減量を行ったのち、水洗、脱水、乾燥する減量加工を行った。
前記水溶液のpHは11.8であった。
減量率を、表1に示す。
Example 2
Treated cloth:
Using the weft knitted fabric prepared in Example 1 and using a mini color dyeing machine (multicolor rotary pot dyeing tester manufactured by Texam Giken Co., Ltd.), 40 g / L of potassium carbonate, the mass of the weft knitted fabric and After the alkali reduction was performed at a ratio of 1:20 to the mass of the aqueous solution of sodium carbonate and the aqueous solution temperature of 100 ° C. for 30 minutes, the reduction in weight was carried out by washing with water, dehydration and drying.
The pH of the aqueous solution was 11.8.
The weight loss rates are shown in Table 1.
[比較例3]
比較例1で使用した横編地を使用した以外は、実施例2と同様にして加工編地を得た。
前記水溶液のpHは11.8であった。
減量率を、表1に示す。実施例2と比較して、1/4の減量率であった。
Comparative Example 3
A processed knitted fabric was obtained in the same manner as in Example 2 except that the weft knitted fabric used in Comparative Example 1 was used.
The pH of the aqueous solution was 11.8.
The weight loss rates are shown in Table 1. Compared to Example 2, the weight loss rate was 1/4.
[比較例4]
比較例2で使用した横編地を使用した以外は、実施例2と同様にして加工編地を得た。
前記水溶液のpHは11.8であった。
減量率を、表1に示す。比較例4の編地の減量率は0%であった。
Comparative Example 4
A processed knitted fabric was obtained in the same manner as in Example 2 except that the flat knitted fabric used in Comparative Example 2 was used.
The pH of the aqueous solution was 11.8.
The weight loss rates are shown in Table 1. The weight loss rate of the knitted fabric of Comparative Example 4 was 0%.
[実施例3]
実施例1で作成した横編地を使用し、ミニカラー染色機((株)テクサム技研製、多色回転ポット染色試験機)を用いて、苛性ソーダ(50%)20g/L、前記横編地の質量と前記苛性ソーダの質量との比を1:20、前記水溶液温度100℃で30分間のアルカリ減量を行ったのち、水洗、脱水、乾燥する減量加工を行った。
前記水溶液のpHは13.8であった。
減量率を、表1に示す。
[Example 3]
Caustic soda (50%) 20 g / L, using the weft knitted fabric prepared in Example 1 and using a mini color dyeing machine (multicolor rotary pot dyeing tester manufactured by Texam Giken Co., Ltd.), said weft knitted fabric The alkali weight loss was carried out at a ratio of the weight of sodium hydroxide to the weight of caustic soda at 1:20 and the aqueous solution temperature at 100 ° C. for 30 minutes, followed by weight loss processing such as washing with water, dehydration and drying.
The pH of the aqueous solution was 13.8.
The weight loss rates are shown in Table 1.
[比較例5]
比較例1で使用した横編地を使用した以外は、実施例3と同様にして加工編地を得た。
前記水溶液のpHは13.8であった。
減量率を、表1に示す。実施例3と比較して、1/2の減量率であった。
Comparative Example 5
A processed knitted fabric was obtained in the same manner as in Example 3 except that the weft knitted fabric used in Comparative Example 1 was used.
The pH of the aqueous solution was 13.8.
The weight loss rates are shown in Table 1. The weight loss rate was 1/2 compared to Example 3.
[比較例6]
比較例2で使用した横編地を使用した以外は、実施例3と同様にして加工編地を得た。
前記水溶液のpHは13.8であった。
減量率を、表1に示す。実施例3と比較して、1/39の減量率であった。
Comparative Example 6
A processed knitted fabric was obtained in the same manner as in Example 3 except that the weft knitted fabric used in Comparative Example 2 was used.
The pH of the aqueous solution was 13.8.
The weight loss rates are shown in Table 1. As compared to Example 3, the weight loss rate was 1/39.
表1に示されるように、炭酸ナトリウムでアルカリ減量を行った場合、実施例1の改質ポリエステル繊維は比較例1の一般的なカチオン可染ポリエステル繊維に比べ減量率が高い結果となり、比較例2のレギュラーポリエステル繊維は炭酸ナトリウムではアルカリ減量が行えなかった。また、炭酸カリウムでアルカリ減量を行った場合、実施例2の改質ポリエステル繊維は比較例3の一般的なカチオン可染ポリエステル繊維に比べ減量率が高い結果となり、比較例4のレギュラーポリエステル繊維は炭酸カリウムではアルカリ減量が行えなかった。苛性ソーダでアルカリ減量を行った場合、実施例3の改質ポリエステル繊維は比較例5の一般的なカチオン可染ポリエステル繊維、比較例6のレギュラーポリエステル繊維に比べて高い減量率となった。 As shown in Table 1, when alkali reduction is performed with sodium carbonate, the modified polyester fiber of Example 1 has a higher weight loss rate than the general cationic dyeable polyester fiber of Comparative Example 1, and the comparative example The regular polyester fiber of No. 2 could not be reduced by alkali with sodium carbonate. In addition, when alkali reduction is performed with potassium carbonate, the modified polyester fiber of Example 2 has a higher weight loss rate than the general cationic dyed polyester fiber of Comparative Example 3, and the regular polyester fiber of Comparative Example 4 has With potassium carbonate, alkali reduction could not be performed. When alkali reduction was performed with caustic soda, the modified polyester fiber of Example 3 had a higher weight loss rate than the general cationic dyed polyester fiber of Comparative Example 5 and the regular polyester fiber of Comparative Example 6.
[実施例4]
被処理布帛:
実施例1で使用した改質ポリエステル繊維と比較例2で使用したレギュラーポリエステル繊維とを使用した経編地(改質ポリエステル繊維=16.7%、レギュラーポリエステル繊維=83.4%)を用い、抜蝕加工剤は以下の組成の抜蝕加工剤を用いた。
・ソルビトーゼC−5(10%水溶液)(Avebe社製) 50質量%
・炭酸ナトリウム((株)トクヤマ社製、商品名:ソーダ灰) 10質量%
・水 40質量%
上記の抜蝕加工剤で、被処理布帛に四角の柄を印捺し、110℃×2分間乾燥を行った。次いで、HTスチーマーを使用して180℃×8分の過熱蒸気処理を行った。その後、ラッコールISF(明成化学工業社製、ノニオン界面活性剤)2g/Lのソーピング浴で80℃×20分間洗浄したのち、水洗、脱水、乾燥させ、抜蝕加工された布帛を得た。
Example 4
Treated cloth:
A warp knitted fabric (modified polyester fiber = 16.7%, regular polyester fiber = 83.4%) using the modified polyester fiber used in Example 1 and the regular polyester fiber used in Comparative Example 2 As the removal processing agent, a removal processing agent having the following composition was used.
・ Sorbitose C-5 (10% aqueous solution) (Avebe) 50% by mass
-Sodium carbonate (manufactured by Tokuyama Corp., trade name: soda ash) 10% by mass
-Water 40% by mass
A square pattern was printed on the treated fabric with the above-mentioned scraping agent, and drying was performed at 110 ° C. for 2 minutes. Next, superheated steam treatment was performed at 180 ° C. for 8 minutes using an HT steamer. Then, after wash | cleaning by 80 degreeC * 20 minutes with the soaping bath of 2 g / L of Laccor ISF (Aeisei Chemical Industry Co., Ltd. make, nonionic surfactant), water washing, dehydration, drying was carried out, and the fabric which carried out the caries processing was obtained.
評価:抜蝕性を目視にて評価した。評価基準として、抜蝕性については印捺部に抜蝕を行った繊維が目視で確認できないものを◎とし、目視で残渣の確認はできるが抜蝕が行えており、商品として使用可能なものと判断できるものを○とし、目視で残渣の確認ができ抜蝕が行えておらず、商品として使用不可と判断できるものを×とした。また、抜蝕部分の破裂強度をJIS L 1018 ミューレン法に準じ測定した。その結果を表2に示す。非抜蝕部分の経編地の破裂強度は804kPaであった。 Evaluation: The peelability was visually evaluated. As the evaluation criteria, for the removal property, fibers which can not be visually checked in the imprinted part are regarded as ◎, and the residue can be checked visually but the removal is possible, and it can be used as a product Those which could be judged as ○, those which could be visually checked for residues, not being able to be removed, and those which could be judged to be unusable as goods were regarded as x. Further, the burst strength of the removed portion was measured according to JIS L 1018 Murren method. The results are shown in Table 2. The burst strength of the warp knitted fabric of the non-prevented portion was 804 kPa.
[実施例5]
糊液組成を表2に示す通り、抜蝕促進剤(明成化学工業社製、メイプリンターOP−2)を使用した以外は実施例4と同様にして抜蝕加工布帛を得た。その抜蝕性評価を表2に示す。
前記抜蝕促進剤を使用することで、抜蝕性は、強アルカリを使用したときと同様の抜蝕性が得られた。一方、破裂強度の低下は少なかった。
[Example 5]
As shown in Table 2, the paste solution composition was subjected to the same procedure as in Example 4 except that a corrosion promoter (made by Meisei Chemical Industry Co., Ltd., May Printer OP-2) was used, to obtain a fabric subjected to a dental erosion process. Table 2 shows the evaluation of its dismovability.
With the use of the above-mentioned removal accelerator, the same removal performance as when using a strong alkali was obtained. On the other hand, the decrease in burst strength was small.
[比較例7、8]
抜蝕加工剤を表2に示す各組成及び条件とした他は実施例2と同様にして抜蝕加工を行い、得られた抜蝕加工布帛を評価した。その結果を表2に示す。
アルカリ性が強いため、抜蝕性は良好であったが、破裂強度の低下が大きかった。
[Comparative Examples 7 and 8]
In the same manner as in Example 2 except that each composition and conditions shown in Table 2 were used as the scraping agent, the scraping process was performed, and the resulting scraped fabric was evaluated. The results are shown in Table 2.
Since the alkalinity was strong, the carriability was good, but the reduction in burst strength was large.
表2に示される通り、炭酸ナトリウムのみを含有した実施例4では抜蝕加工を行うことができ、抜蝕部の強度低下も少なかった。一方、炭酸グアニジンを用いた比較例7、水酸化ナトリウムを用いた比較例8は抜蝕部の抜蝕性は良好だが抜蝕部の極端な強度低下が見られた。
炭酸グアニジンを使用した加工剤はpH11.8であるが、炭酸グアニジンは加熱すると強アルカリになることが知られており、そのため破裂強度の低下が大きくなった。
また、抜蝕促進剤であるメイプリンターOP−2と炭酸ナトリウムとを含有した実施例5では良好な抜蝕性が得られ、抜蝕部の強度低下も少なかった。
As shown in Table 2, in Example 4 in which only sodium carbonate was contained, it was possible to carry out the erosion process, and there was little reduction in the strength of the ejected portion. On the other hand, in Comparative Example 7 using guanidine carbonate and Comparative Example 8 using sodium hydroxide, the removal property of the removed portion was good, but an extreme decrease in strength of the removed portion was observed.
Although the processing agent using guanidine carbonate has a pH of 11.8, it is known that guanidine carbonate becomes strongly alkaline upon heating, so that the reduction in burst strength is increased.
In addition, in Example 5 containing Mayprinter OP-2 which is a caries removal accelerator and sodium carbonate, good cariesability was obtained, and the reduction in strength of the carious part was small.
[実施例6]
被処理布帛を実施例1と同じ改質ポリエステル繊維と、比較例2と同じレギュラーポリエステル繊維(帝人(株)社製、84dtex)とを使用した編物(改質ポリエステル繊維50%/レギュラーポリエステル繊維50%)を用いた以外は実施例5と同様にして抜蝕加工を行い、抜蝕加工布帛を得た。その抜蝕性評価を表3に示す。評価基準として、抜蝕性については印捺部に抜蝕を行った繊維が目視で確認できないものを◎とし、目視で残渣の確認はできるが抜蝕が行えており、商品として使用可能なものと判断できるものを○とし、目視で残渣の確認ができ抜蝕が行えておらず、商品として使用不可と判断できるものを×とした。
[Example 6]
A knitted fabric (modified polyester fiber 50% / regular polyester fiber 50) in which the treated fabric is the same modified polyester fiber as in Example 1 and the same regular polyester fiber as in Comparative Example 2 (84 dtex manufactured by Teijin Limited) In the same manner as in Example 5 except that%) was used, a removal process was performed to obtain a removed fabric. Table 3 shows the evaluation of its dismovability. As the evaluation criteria, for the removal property, fibers which can not be visually checked in the imprinted part are regarded as ◎, and the residue can be checked visually but the removal is possible, and it can be used as a product Those which could be judged as ○, those which could be visually checked for residues, not being able to be removed, and those which could be judged to be unusable as goods were regarded as x.
[比較例9〜12]
実施例4の改質ポリエステル繊維を、表3に記載されたポリエステル繊維に変えた以外は、実施例4と同様にして抜蝕加工布帛を得た。その抜蝕性評価を表3に示す。
[Comparative Examples 9 to 12]
In the same manner as in Example 4 except that the modified polyester fiber of Example 4 was changed to the polyester fiber described in Table 3, a removal-processed fabric was obtained. Table 3 shows the evaluation of its dismovability.
本発明によれば、変性ポリエステル繊維に改質ポリエステル繊維を使用することで、改質ポリエステル繊維と未変性ポリエステル繊維とからなる織編物にアルカリ減量を行わずに印捺部の改質ポリエステル繊維のみを除去し、未変性ポリエステル繊維の脆化を起こさない、改質ポリエステル繊維の抜蝕性が良好な抜蝕加工布を得ることが可能であり、人に対して有害性の高い強アルカリ性物質を用いていないため、作業上安全性の高い抜蝕加工が可能となる。 According to the present invention, by using the modified polyester fiber as the modified polyester fiber, only the modified polyester fiber of the printing section is subjected to the alkali-knitting without being reduced in the woven and knitted fabric made of the modified polyester fiber and the unmodified polyester fiber. It is possible to obtain a scraped treated cloth which is excellent in corrosion resistance of the modified polyester fiber by eliminating the embrittlement of the unmodified polyester fiber, and which is highly harmful to humans. Since it is not used, it is possible to perform high-safety corrosion-removing work.
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TW104136397A TWI612190B (en) | 2015-07-15 | 2015-11-05 | Modified polyester fiber, burnt-processed knitted fabric containing same fiber, and manufacturing method thereof |
US15/743,429 US20180209074A1 (en) | 2015-07-15 | 2015-11-06 | Modified polyester fiber, etching finished woven and knitted fabric containing the fiber, and method for producing same |
PCT/JP2015/081399 WO2017010024A1 (en) | 2015-07-15 | 2015-11-06 | Modified polyester fiber, opal finished woven and knitted fabric containing the fiber, and method for producing same |
EP15898335.3A EP3323913A4 (en) | 2015-07-15 | 2015-11-06 | Modified polyester fiber, opal finished woven and knitted fabric containing the fiber, and method for producing same |
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JP2020076182A (en) * | 2018-11-05 | 2020-05-21 | 三菱ケミカル株式会社 | Knitted fabric having partial opal finish part |
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Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS58115181A (en) * | 1981-12-24 | 1983-07-08 | 三菱レイヨン株式会社 | Production of continuous yarn dyed processed yarn |
EP0177014B1 (en) * | 1984-10-03 | 1991-01-02 | Teijin Limited | Modified polyester fiber and process for preparation thereof |
US5059482A (en) * | 1988-09-13 | 1991-10-22 | Kuraray Company, Ltd. | Composite fiber and process for producing the same |
US4990594A (en) * | 1990-03-07 | 1991-02-05 | Hoechst Celanese Corporation | Producing a copolyester from a lower dialkyl ester of terephthalic acid, a glycol and a dicarboxylic acid |
TW211030B (en) * | 1991-10-01 | 1993-08-11 | Du Pont | |
JP2004225192A (en) * | 2003-01-23 | 2004-08-12 | Mitsubishi Rayon Co Ltd | Polyester fiber for etching, etched polyester fabric and method for producing etched polyester fabric |
JP5367261B2 (en) * | 2005-12-26 | 2013-12-11 | 三菱レイヨン株式会社 | Fabric having partially different stretch properties and method for producing the same |
US20130232937A1 (en) * | 2007-01-23 | 2013-09-12 | Reliance Industries Limited | Easily alkali soluble polyester and method for producing the same |
TW200905029A (en) * | 2007-07-30 | 2009-02-01 | Men Chuen Fibre Industry Co Ltd | A manufacturing method of burn-out for tricot |
JP5726002B2 (en) * | 2011-07-07 | 2015-05-27 | 三菱レイヨン・テキスタイル株式会社 | POLYESTER RESIN COMPOSITION, PROCESS FOR PRODUCING THE RESIN COMPOSITION, POLYESTER FIBER COMPRISING THE RESIN COMPOSITION, AND FIBER PRODUCT |
JP6379643B2 (en) * | 2014-05-07 | 2018-08-29 | 三菱ケミカル株式会社 | Modified polyester fiber and its mixed goods |
-
2015
- 2015-07-15 JP JP2015141163A patent/JP6515715B2/en active Active
- 2015-11-05 TW TW104136397A patent/TWI612190B/en active
- 2015-11-06 WO PCT/JP2015/081399 patent/WO2017010024A1/en active Application Filing
- 2015-11-06 EP EP15898335.3A patent/EP3323913A4/en not_active Withdrawn
- 2015-11-06 US US15/743,429 patent/US20180209074A1/en not_active Abandoned
Also Published As
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EP3323913A1 (en) | 2018-05-23 |
US20180209074A1 (en) | 2018-07-26 |
WO2017010024A1 (en) | 2017-01-19 |
JP2017020147A (en) | 2017-01-26 |
EP3323913A4 (en) | 2018-07-11 |
TW201702444A (en) | 2017-01-16 |
TWI612190B (en) | 2018-01-21 |
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