JPH04163336A - Preparation of warp - Google Patents
Preparation of warpInfo
- Publication number
- JPH04163336A JPH04163336A JP28580590A JP28580590A JPH04163336A JP H04163336 A JPH04163336 A JP H04163336A JP 28580590 A JP28580590 A JP 28580590A JP 28580590 A JP28580590 A JP 28580590A JP H04163336 A JPH04163336 A JP H04163336A
- Authority
- JP
- Japan
- Prior art keywords
- yarn
- acid
- warp
- water
- direct
- 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
- 238000002360 preparation method Methods 0.000 title claims abstract description 6
- 238000009941 weaving Methods 0.000 claims abstract description 16
- 239000000203 mixture Substances 0.000 claims abstract description 12
- 238000001035 drying Methods 0.000 claims abstract description 7
- 239000012209 synthetic fiber Substances 0.000 claims abstract description 7
- 229920002994 synthetic fiber Polymers 0.000 claims abstract description 7
- 229920001169 thermoplastic Polymers 0.000 claims abstract description 6
- 239000004416 thermosoftening plastic Substances 0.000 claims abstract description 6
- 238000004804 winding Methods 0.000 claims abstract 2
- 238000000034 method Methods 0.000 claims description 27
- 239000003292 glue Substances 0.000 claims description 16
- -1 acrylic ester Chemical class 0.000 claims description 15
- 239000000839 emulsion Substances 0.000 claims description 4
- 238000004513 sizing Methods 0.000 abstract description 16
- 235000014676 Phragmites communis Nutrition 0.000 abstract description 3
- 238000005422 blasting Methods 0.000 abstract 1
- 239000001993 wax Substances 0.000 description 12
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 11
- 239000002253 acid Substances 0.000 description 11
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 7
- 239000003795 chemical substances by application Substances 0.000 description 6
- 239000002759 woven fabric Substances 0.000 description 6
- 125000004432 carbon atom Chemical group C* 0.000 description 5
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 4
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 4
- 125000001931 aliphatic group Chemical group 0.000 description 4
- 239000004744 fabric Substances 0.000 description 4
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- 150000002009 diols Chemical class 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 229920001225 polyester resin Polymers 0.000 description 3
- 239000004645 polyester resin Substances 0.000 description 3
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 2
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 239000012190 activator Substances 0.000 description 2
- 238000004026 adhesive bonding Methods 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 125000002723 alicyclic group Chemical group 0.000 description 2
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 235000013869 carnauba wax Nutrition 0.000 description 2
- 239000004203 carnauba wax Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 150000001991 dicarboxylic acids Chemical class 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- WLJVNTCWHIRURA-UHFFFAOYSA-N pimelic acid Chemical compound OC(=O)CCCCCC(O)=O WLJVNTCWHIRURA-UHFFFAOYSA-N 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 229920001451 polypropylene glycol Polymers 0.000 description 2
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
- 238000009991 scouring Methods 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 description 2
- 239000004753 textile Substances 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 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
- JHPBZFOKBAGZBL-UHFFFAOYSA-N (3-hydroxy-2,2,4-trimethylpentyl) 2-methylprop-2-enoate Chemical compound CC(C)C(O)C(C)(C)COC(=O)C(C)=C JHPBZFOKBAGZBL-UHFFFAOYSA-N 0.000 description 1
- FFJCNSLCJOQHKM-CLFAGFIQSA-N (z)-1-[(z)-octadec-9-enoxy]octadec-9-ene Chemical compound CCCCCCCC\C=C/CCCCCCCCOCCCCCCCC\C=C/CCCCCCCC FFJCNSLCJOQHKM-CLFAGFIQSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- BCBHDSLDGBIFIX-UHFFFAOYSA-N 4-[(2-hydroxyethoxy)carbonyl]benzoic acid Chemical compound OCCOC(=O)C1=CC=C(C(O)=O)C=C1 BCBHDSLDGBIFIX-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- KMTRUDSVKNLOMY-UHFFFAOYSA-N Ethylene carbonate Chemical compound O=C1OCCO1 KMTRUDSVKNLOMY-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000003522 acrylic cement Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 235000013871 bee wax Nutrition 0.000 description 1
- 239000012166 beeswax Substances 0.000 description 1
- 229940092738 beeswax Drugs 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-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
- 235000013868 candelilla wax Nutrition 0.000 description 1
- 239000004204 candelilla wax Substances 0.000 description 1
- 229940073532 candelilla wax Drugs 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 229940082483 carnauba wax Drugs 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- OIWOHHBRDFKZNC-UHFFFAOYSA-N cyclohexyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC1CCCCC1 OIWOHHBRDFKZNC-UHFFFAOYSA-N 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- GMSCBRSQMRDRCD-UHFFFAOYSA-N dodecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCOC(=O)C(C)=C GMSCBRSQMRDRCD-UHFFFAOYSA-N 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
- 238000004043 dyeing Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- IUJAMGNYPWYUPM-UHFFFAOYSA-N hentriacontane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC IUJAMGNYPWYUPM-UHFFFAOYSA-N 0.000 description 1
- 150000004677 hydrates Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- 230000007794 irritation Effects 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([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
- QANMHLXAZMSUEX-UHFFFAOYSA-N kinetin Chemical compound N=1C=NC=2N=CNC=2C=1NCC1=CC=CO1 QANMHLXAZMSUEX-UHFFFAOYSA-N 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 239000012170 montan wax Substances 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
- 239000008041 oiling agent Substances 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 235000013873 oxidized polyethylene wax Nutrition 0.000 description 1
- 239000004209 oxidized polyethylene wax Substances 0.000 description 1
- 125000000913 palmityl 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])[H] 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 229920000259 polyoxyethylene lauryl ether Polymers 0.000 description 1
- 229920000137 polyphosphoric acid Polymers 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 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 1
- 239000000126 substance Substances 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 229940045860 white wax Drugs 0.000 description 1
Landscapes
- Treatment Of Fiber Materials (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Yarns And Mechanical Finishing Of Yarns Or Ropes (AREA)
- Warping, Beaming, Or Leasing (AREA)
Abstract
Description
【発明の詳細な説明】
[産業上の利用分野1
本発明は、経糸の準備方法に関するもであり、さらに詳
しくは、整経工程において経糸を直接製織用のビームに
巻き取る経糸の準備方法に関するものである。DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field 1] The present invention relates to a method for preparing warp threads, and more particularly, to a method for preparing warp threads in which warp threads are directly wound around a beam for weaving in a warping process. It is something.
[従来技術]
従来、有杼織機や無杼m機に使用する経糸が無撚糸の場
合には通常整経工程、糊(=J工程、ビーミンク工程を
経て製織用のビームに巻き取りこれにより製織作業を行
っていた。かがる工程の中では、糊付工程の生産性が最
も悪い。すなわち、糊付工程においては、糊(=1され
た糸の乾燥のために糸の移送速度を低下させる必要があ
り、乾燥のための多量の熱エネルギーを消費することも
ニス1ヘアツブの要因になり問題であった。このため整
経工程において糊付工程を省略できれば著しい時間短縮
ができ、エネルギーの節減が可能となる。その様な試み
として、経糸に有撚糸又はインターレース加工系を用い
て無糊で整経を行う方法が提案された。しかし、近年の
ように製織]二程の高速化、又は、織物の高密度化、用
いる原糸の多様化により有撚、又はインターレース系を
便用しても無糊では製織工程の効率が低下する場合がで
てきた。[Prior art] Conventionally, when the warp yarns used in shuttled looms and shuttleless looms are non-twisted yarns, they are usually passed through a warping process, a gluing process, a beam minking process, and then wound onto a beam for weaving. Among the darning processes, the sizing process has the lowest productivity.In other words, in the sizing process, the thread transport speed is reduced to dry the sizing thread. It was a problem that a large amount of thermal energy was consumed for drying, which caused hair lumps in the varnish.For this reason, if the gluing process could be omitted in the warping process, it would be possible to significantly shorten the time and save energy. As such, a method of warping without glue using twisted or interlaced warp threads has been proposed. Furthermore, due to the increased density of textiles and the diversification of the yarns used, even if twisted or interlaced textiles are conveniently used, there are cases where the efficiency of the weaving process is lowered if the weaving process is performed without glue.
このなめ、特開昭60−28583号公報に記載されて
ぃるように合成繊維フィラメント糸のサイジングを施し
た後乾娯することなく巻き取り製織する方法が撞案され
ているが、経糸に付与した糊を乾燥しないで用いると糸
が通過するガイド等に糊スカムが滞積し、通過する糸質
を損ね、糸に毛羽を発生させるなどの問題か生じるよう
になる。また、インターレースされた糸を使用した場合
には、糊付けにより該交絡部が製織中でも解除されず繊
物中にインターレースにより交絡部分の大部分が残留し
、経糸、緯糸にフィラメント糸を使用した織物では経糸
方向の微少な光沢斑や、イラツキの原因となり好ましく
ない。To solve this problem, a method has been proposed in which the synthetic fiber filament yarn is sized and then wound and woven without drying, as described in Japanese Patent Application Laid-open No. 60-28583. If the glue is used without drying, glue scum will accumulate on the guides through which the threads pass, damaging the quality of the threads passing through and causing problems such as fluffing of the threads. In addition, when interlaced yarns are used, the entangled portions are not released during weaving due to sizing, and most of the interlaced portions remain in the fabric, and in fabrics using filament yarns for the warp and weft, This is undesirable as it causes minute gloss spots in the warp direction and irritation.
[発明の目的]
本発明の目的は、インターレース糸を用いてダイレクト
ワーパーで整経する際に水溶性糊組成物を付着させて直
接製織用のビームに巻き取る経糸準備方法を製造する方
法を提供することにある。[Object of the Invention] An object of the present invention is to provide a method for manufacturing warp yarns, in which a water-soluble glue composition is attached during warping with a direct warper using interlaced yarns, and the warp yarns are directly wound onto a beam for weaving. It's about doing.
「発明の構成」
本発明は、交絡数が10〜60ゲ/mの範囲にインター
レース処理された熱可塑性合成繊維マルチフィラメント
糸をダイレクI−ワーパーに供給して水溶性糊組成物を
付着させ、該糊付糸を常温にて送風乾燥しながら直接製
織用ビームに巻き取ることを特徴とする経糸準備方法に
あり、該水溶性糊組成物としては、アクリルエステル系
糊剤が好ましく使用され、該アクリルエステル系糊剤に
ワックスエマルジョンを混合させたものが好ましく例示
される。"Structure of the Invention" The present invention provides a thermoplastic synthetic fiber multifilament yarn interlaced with a number of entanglements in the range of 10 to 60 g/m to a Directrec I-warper to adhere a water-soluble glue composition, The warp preparation method is characterized in that the sized yarn is directly wound around a weaving beam while being blown and dried at room temperature, and the water-soluble sizing composition is preferably an acrylic ester sizing agent. A preferred example is one in which an acrylic ester adhesive is mixed with a wax emulsion.
第1図は、本発明の方法において行われるダイレクトワ
ーパーにて水溶性糊組成物を付着させる工程の例を示す
工程図である。FIG. 1 is a process diagram showing an example of the step of applying a water-soluble glue composition using a direct warper, which is performed in the method of the present invention.
第1図において、多数の原糸ボビン1から供給される糸
はティクアップローラー2を経てシート状に並べられ、
糊イ」ローラー4に接触して移送される際に糊付けされ
る。該糊付けされたシート状糸は、ガイド筬5に至るま
でに送風機(図示せず)に連結されている送風パイプ9
から噴き出される空気により乾燥される。該送風パイプ
9はシート状糸の幅方向に亘って設置されており、該送
風パイプ9には該シート状糸に対向してスリットが形成
され、該スリットより送風できるものを使用する。次い
で、該ガイド筬5をでたシート状糸は副長ローラー6を
経て製織ビーム8に巻き取られる。In FIG. 1, yarns supplied from a large number of yarn bobbins 1 are arranged in a sheet shape after passing through a pick-up roller 2.
Glue is applied when it comes into contact with the glue roller 4 and is transferred. The glued sheet-like yarn passes through a blower pipe 9 connected to a blower (not shown) before reaching the guide reed 5.
It is dried by the air blown out. The blower pipe 9 is installed across the width direction of the sheet-like yarn, and the blower pipe 9 has a slit formed opposite to the sheet-like yarn, and is capable of blowing air through the slit. Next, the sheet-like yarn leaving the guide reed 5 passes through a sub-length roller 6 and is wound around a weaving beam 8.
7はプレスロールである。該送風機から送り出される空
気は、加熱したものを使用する必要はなく室温の温度の
ものか使用される。7 is a press roll. The air sent out from the blower does not need to be heated; instead, air at room temperature is used.
本発明に使用される糸はインターレース処理された熱可
塑性合成繊維マルチフィラメント糸であって、公知の手
段によりインターレース処理が施されており該インター
レースの交絡数は10〜60ゲの範囲にあるものが使用
される。該交絡数が10ゲ/m未満では、糸の集束性が
不足し製織することができず、また、交絡数が60ゲ/
m超える場合には製織した織物の中にインターレース糸
による交絡が残りいずれの場合にも問題となり好ましく
ない。また、該熱可塑性合成繊維マルチフィラメント糸
を構成するフィラメントの単糸デニールは1デニ一ル以
上のものを使用することが好ましい。The yarn used in the present invention is an interlaced thermoplastic synthetic fiber multifilament yarn, which has been interlaced by a known method, and the number of interlaces is in the range of 10 to 60 yarns. used. If the number of entanglements is less than 10 ge/m, the threads will not have sufficient convergence and cannot be woven;
If it exceeds m, entanglement due to interlace yarns will remain in the woven fabric, which is not preferable. Further, it is preferable to use a single filament denier of 1 denier or more of the filaments constituting the thermoplastic synthetic fiber multifilament yarn.
該単糸デニールが1デニ一ル未満の場合には、マルチフ
ィラメント糸の構成単糸本数が増加し、乾−、−5−
無効率が十分でない恐れがあり好ましくない。If the single yarn denier is less than 1 denier, the number of single yarns constituting the multifilament yarn increases and the dry efficiency may not be sufficient, which is not preferable.
本発明に使用する水溶性a +tJl成物は、炭素数が
1〜24の脂肪族アルコールのアクリル酸エステルおよ
び/又はメタクリル酸エステル75〜92重量%とアク
リル酸および゛メタクリル酸の混合!l!125〜8重
景%からなる単量体80〜99,9重量%に対してジカ
ルボン酸、又はジカルボン酸に水酸基およびカルボキシ
ル基を各1個有するオキシ酸併用のものとポリエチレン
グリコールを必須成分とするジオール又はそれらのエス
テル形成誘導体をリン酸、ピロール酸、ポリリン酸、亜
リン酸、メタンスホン酸の少なくとも1種を添加して反
応させ、次いで水酸化アルカリ金属、アンモニア水、ア
ルカノールアミンの少なくとも1種で中和してなる水溶
性ポリエステル樹脂20〜0.1重量%を添加して、炭
素数1〜3の脂肪族アルコール又は炭素数1〜3の脂肪
族アルコールと水の温媒にて溶液重合しく分子量5〜1
0万のものが好ましく使用される)、次いで水酸化アル
カリ金属、アンモニア水、アルカノールアミンの少なく
とも1種で中和してなる− 6 =
変性水溶性アクリル系糊剤が例示される。The water-soluble a+tJl composition used in the present invention is a mixture of acrylic ester and/or methacrylic ester of an aliphatic alcohol having 1 to 24 carbon atoms in an amount of 75 to 92% by weight, and acrylic acid and methacrylic acid. l! The essential components are dicarboxylic acid, dicarboxylic acid combined with oxyacid having one hydroxyl group and one carboxyl group, and polyethylene glycol for 80 to 99.9% by weight of monomer consisting of 125 to 8 weight percent. Diols or their ester-forming derivatives are reacted by adding at least one of phosphoric acid, pyrolic acid, polyphosphoric acid, phosphorous acid, and methanesphonic acid, and then reacted with at least one of alkali metal hydroxide, aqueous ammonia, and alkanolamine. Add 20 to 0.1% by weight of a neutralized water-soluble polyester resin and carry out solution polymerization in a hot medium of an aliphatic alcohol having 1 to 3 carbon atoms or an aliphatic alcohol having 1 to 3 carbon atoms and water. Molecular weight 5-1
00,000 is preferably used), and then neutralized with at least one of alkali metal hydroxide, aqueous ammonia, and alkanolamine.
上記において、炭素数1〜24の脂肪族アルコールのア
クリル酸エステル、メタクリル酸ニスデルとしては、例
えは、メチル、エチル、プロピル、イソプロピル、ブチ
ル、イソブチル、ターシャリブチル、オクチル、2−エ
チルヘキシル、ラウリル、ミスチル、セチル、ステアリ
ル、アラキニル、テトラコザノールなどのアクリル酸エ
ステル、メタクリル酸エステルがある。なお、上記のよ
うな単量体に共重合可能な重量体、例えば、酢酸ビニル
、ピロピオン酸ビニル、スヂレン、アクリルアマイド、
メタクリルアマイド、タイアセトンアクリルアマイド、
アクリルニ1〜リル、メタアクリルニトリル、シクロへ
キシルメタクリレ−1〜などの共重合を制限するもので
はない。また、前記における水溶性ポリエステル樹脂を
1!1造するためのジカルボン酸は脂肪族、脂環族、又
は芳香族であってもよい。そのようなジカルボン酸の例
は、シュウ酸、マロン酸、ジカルボン酸、コハク酸、ク
ルタール酸、アジピン酸、ピメリン酸、マゼライン酸、
セバシン酸、フマール酸、マレイン酸、イタコン酸、フ
タール酸、テレフタール酸、イソフタール酸などがある
。口し、ジカルボン酸には」1記の酸に対する酸勲水物
、エステル、および酸クロライドが含まれる。また、オ
キシ酸は脂肪族、又は、芳香族てあってもよく、そのよ
うなオキシ酸の例はm、p−オキシ安息香酸、クリコー
ル酸、乳酸、ヒト17キシアクリル酸、ザルチル酸、マ
デン酸、l−ロッパ酸、β−ヒドロキシエチルテレフタ
レー1〜などがある。また、ジオールとしては、ポリエ
チレングリコールを必須成分として含み、これを脂肪族
、脂環族、芳香族ジオールを江意に併用することができ
る。そのようなジオールの例は、ポリプロピレングリコ
ール、エチレンクリコール、プV7ピレンクリコール、
1.3−プロパンジオール、1,3−ブタンジオール、
1.4−ブタンジオール、L5−ベンタンジオール、1
.6−ヘキサジオール、4,4−メチレンシフ〕−二−
ル、2.5−ナフタレンジオール、エチレンカーポネー
1〜などを含む。In the above, examples of the acrylic ester of an aliphatic alcohol having 1 to 24 carbon atoms and Nisdel methacrylate include methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tert-butyl, octyl, 2-ethylhexyl, lauryl, There are acrylic esters and methacrylic esters such as mystyl, cetyl, stearyl, araquinyl, and tetracozanol. In addition, heavy substances copolymerizable with the above monomers, such as vinyl acetate, vinyl propionate, styrene, acrylamide,
methacrylamide, tiacetone acrylamide,
It does not limit the copolymerization of acrylonitrile, methacrylonitrile, cyclohexylmethacrylate, and the like. Further, the dicarboxylic acid for producing the water-soluble polyester resin 1:1 in the above may be aliphatic, alicyclic, or aromatic. Examples of such dicarboxylic acids are oxalic acid, malonic acid, dicarboxylic acid, succinic acid, cultaric acid, adipic acid, pimelic acid, mazelaic acid,
These include sebacic acid, fumaric acid, maleic acid, itaconic acid, phthalic acid, terephthalic acid, and isophthalic acid. In general, dicarboxylic acids include acid hydrates, esters, and acid chlorides of the acids listed in item 1 above. The oxyacid may also be aliphatic or aromatic; examples of such oxyacids include m, p-oxybenzoic acid, glycolic acid, lactic acid, human 17-oxyacrylic acid, salicylic acid, madenic acid. , l-loppaic acid, β-hydroxyethyl terephthalate 1-, and the like. Further, the diol includes polyethylene glycol as an essential component, and this can be used in combination with aliphatic, alicyclic, and aromatic diols. Examples of such diols are polypropylene glycol, ethylene glycol, polypropylene glycol,
1.3-propanediol, 1,3-butanediol,
1.4-butanediol, L5-bentanediol, 1
.. 6-hexadiol, 4,4-methylene Schiff]-2-
2,5-naphthalene diol, ethylene carbonate, etc.
さらに、本発明においては該変性水溶性アクリル系糊剤
25〜75重量%に、融点50’C以十、ゲン化価10
〜200を有する天然ワックスおよび/又は、合成ワッ
クスからなるワックスエマルジョン75〜25重景%が
混合されていてもよい。天然ワックス、としてはカルナ
バワックス、カンデリラワックス、蜜ロウ、白ロウ、モ
ンタンワックス、ぬか冒つなどを、また、合成ワックス
としては、酸化ポリエチレンワックス、酸化ワックス、
ソウビタン、ペンタエリストール、グリセリン、エチレ
ングリコールと炭素数14〜24の脂肪族とのエステル
によって得られるワックスなどが例示される。なお、該
エマルジョン化には通常の非イオン活性剤、およびアニ
オン活性剤を使用ずれはよい。Furthermore, in the present invention, 25 to 75% by weight of the modified water-soluble acrylic adhesive has a melting point of 50'C or higher and a genification value of 10.
A wax emulsion consisting of natural waxes and/or synthetic waxes having a weight of 75 to 25% may be mixed. Natural waxes include carnauba wax, candelilla wax, beeswax, white wax, montan wax, bran wax, etc. Synthetic waxes include oxidized polyethylene wax, oxidized wax,
Examples include sourbitane, pentaerythritol, glycerin, and waxes obtained by esters of ethylene glycol and aliphatics having 14 to 24 carbon atoms. Note that for the emulsification, ordinary nonionic activators and anionic activators may be used.
また、該水溶性糊剤は全経糸量に対して、0.1〜5重
某%が付与されるように調節される。Further, the water-soluble sizing agent is adjusted to be applied in an amount of 0.1 to 5% by weight based on the total amount of warp yarns.
[発明の効果]
本発明方法は以」−のような構成を有するため従来の製
織準備工程における乾燥王稈が省略でき生産効率が向上
する。すなわち、本発明では前記のように水溶性糊組成
物を使用するなめ、従来の乾燥−[程で発生していた問
題点、特に、整経機ての糊スカムの発生、フィラメン1
〜のビーム内固着、製経時の開]]性不良の発生などの
問題点が解決される。また、経糸として交絡部を有する
インターレース糸を(重用し、これに糊付を施した場合
に発生ずる経方向の微小欠点やイラン虞などの問題は発
生しないものである。本発明の方法により得られる織物
では、#A物を構成する糸の残留インターレース交絡数
は5ケ/m以下であり、これによる欠点は大幅に改良さ
れる。[Effects of the Invention] Since the method of the present invention has the following configuration, the drying process in the conventional weaving preparation process can be omitted, improving production efficiency. That is, in the present invention, since the water-soluble glue composition is used as described above, the problems that have occurred in the conventional drying process, especially the generation of glue scum in the warping machine and the filament 1.
Problems such as fixation in the beam of ~, opening during manufacture] and occurrence of defects are solved. In addition, problems such as minute defects in the warp direction and the risk of cracking that occur when an interlaced yarn having entangled portions is used as the warp yarn and sizing is applied to the warp yarn do not occur. In the woven fabric, the number of residual interlace entanglements of the threads constituting the #A material is 5 or less per meter, and the drawbacks caused by this are greatly improved.
さらに、従来の糊付的においては糊剤としては分子量が
15〜30万のものか使用され、精練工程が必要であっ
たが、本発明で「重用する糊剤は該分子量が10万未満
であるので特別な精練工程は不要であり、経糸無糊織物
と同様に染色加工の工程の中で行うことが出来る。Furthermore, in conventional sizing processes, sizing agents with a molecular weight of 150,000 to 300,000 are used, and a scouring process is required. Therefore, there is no need for a special scouring process, and it can be carried out during the dyeing process in the same way as warp-less woven fabric.
[一実施例]
経糸にポリエステルマルチフィラメントda/20f
i l )であって、交絡数50ゲ/1ηのインターレ
ースを施したものを使用し、緯糸にポリエステルマルチ
フィラメンl〜糸(75de/36f i l )を使
用してウォータージェッI−ルームにてMliするに際
して、第1図に示す工程において該経糸に下記に示す成
分を有する糊剤を糸に対して1.0重量%付着せしめた
。[One example] Polyester multifilament da/20f for warp
Mli) with interlacing with a number of entanglements of 50ge/1η was used, and the weft was polyester multifilament yarn (75de/36fil) in a waterjet I-room. In doing so, in the step shown in FIG. 1, 1.0% by weight of a sizing agent having the components shown below was applied to the warp threads.
[糊剤内容]
A、水溶性ポリエステル樹脂
テレフタール酸 5部部イソフタ
ール酸 25部ポリオキシエチレ
ングリコール 50部エチレングリコール
55部亜リン酸
8部B、アクリル酸エステル系糊剤
アクリル酸エチル 20部メタクリ
ル酸ブチル 3部部メタクリル酸メチ
ル 25部メタクリル酸ラウリル
13部アクリル酸
7部メタクリル酸 5部−
11〜
C,ワックスエマルジョン
カルナバワックス 40部力ルデリ
ラワックス 30部モタンワックス
5部ポリオキシエチレンラウリル
エーテル 10部ポリオキシエチレンオレイルエーテル
10部ソルビタンモノオレユー1へ5部
かかる経糸と緯糸を用いて経糸密度:144本/3、7
9cn+、緯糸密度=115本/379CI11により
つ詞−タージェットルームとして津田駒工業(株)製の
のZIll−300タイプを使用して回転数: 700
r、pn+の速度で製織した。製織効率として停台回数
を調べたが従来の糊付した経糸を使用したものと遜色無
い効率か得られた。得られた織物を構成する糸の交絡数
はOゲ/mであり、織物の表面にはイラツキは全く見ら
れず品位の高い織物が得られた。[Sticker content] A, water-soluble polyester resin Terephthalic acid 5 parts Isophthalic acid 25 parts Polyoxyethylene glycol 50 parts Ethylene glycol
55 parts phosphorous acid
8 parts B, acrylic ester type sizing agent Ethyl acrylate 20 parts Butyl methacrylate 3 parts Methyl methacrylate 25 parts Lauryl methacrylate
13 parts acrylic acid
7 parts methacrylic acid 5 parts
11~C, Wax emulsion carnauba wax 40 parts Ruderilla wax 30 parts Motan wax
5 parts polyoxyethylene lauryl ether 10 parts polyoxyethylene oleyl ether 10 parts sorbitan monooleyu 1 to 5 parts Warp density: 144/3, 7
9cn+, weft density = 115 threads/379CI11 - ZIll-300 type manufactured by Tsudakoma Industries Co., Ltd. was used as the target loom; rotation speed: 700
Weaving was carried out at a speed of r, pn+. The number of times the weaving machine stopped was investigated as weaving efficiency, and the efficiency was comparable to that of conventional weaving using glued warp threads. The number of entanglements of the threads constituting the obtained woven fabric was Oge/m, and a high quality woven fabric was obtained with no irregularities observed on the surface of the woven fabric.
比較例1として、従来の糊剤であるプラサイズJ −5
(互応化学]−業(株)製)を使用して実施例と同様の
経糸、緯糸を使用して、同様の織機により製繊した。得
られた織物はイランAがあり織物の品位は満足するもの
がえられなかった。As Comparative Example 1, plasticize J-5, which is a conventional glue, was used.
(manufactured by Gōhō Kagaku Co., Ltd.), using the same warp and weft as in the example, and the same loom. The fabric obtained was Iran A, and the quality of the fabric was not satisfactory.
また、比較例2として、糊剤の代わりにストレートオイ
リング剤:サイテックスS−571(互応化学工業(株
)製)を使用して実施例と同様の経糸、緯糸を使用して
、同様の織機により製織した。得られたm′$Aの品位
は一応満足なものが得られなが、製織稼動率が不良で工
業生産には採用できないものであった。In addition, as Comparative Example 2, a straight oiling agent: Cytex S-571 (manufactured by Gooh Kagaku Kogyo Co., Ltd.) was used instead of the sizing agent, the same warp and weft as in the example were used, and the same loom was used. Woven by. Although the quality of the obtained m'$A was somewhat satisfactory, the weaving operation rate was poor and it could not be adopted for industrial production.
第1表
4、図m16))尚早な説明
第1図は、本発明の方法において行われるタイレクトワ
ーバーにて水溶性a組成物を付着させる工程の例を示す
工程図である。Table 1 4, Figure m16)) Premature Explanation FIG. 1 is a process diagram showing an example of the step of depositing the water-soluble a composition with a direct weaver, which is carried out in the method of the present invention.
Claims (2)
ス処理された熱可塑性合成繊維マルチフィラメント糸を
ダイレクトワーパーに供給して水溶性糊組成物を付着さ
せ、該糊付糸を室温にて送風乾燥しながら直接製織用ビ
ームに巻き取ることを特徴とする経糸準備方法。(1) Thermoplastic synthetic fiber multifilament yarn interlaced with a number of entanglements in the range of 10 to 60 yarns/m is fed to a direct warper, a water-soluble glue composition is applied, and the sized yarn is kept at room temperature. A warp preparation method characterized by winding directly onto a weaving beam while drying with air.
、該アクリルエステル系糊剤にワックスエマルジョンを
混合させたものである請求項(1)の方法。(2) The method according to claim 1, wherein the water-soluble glue composition is an acrylic ester glue, and the acrylic ester glue is mixed with a wax emulsion.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP28580590A JPH04163336A (en) | 1990-10-25 | 1990-10-25 | Preparation of warp |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP28580590A JPH04163336A (en) | 1990-10-25 | 1990-10-25 | Preparation of warp |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH04163336A true JPH04163336A (en) | 1992-06-08 |
Family
ID=17696313
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP28580590A Pending JPH04163336A (en) | 1990-10-25 | 1990-10-25 | Preparation of warp |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH04163336A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2720413A1 (en) * | 1994-05-27 | 1995-12-01 | Rhone Poulenc Fibres | Multifilament polyester thread for weaving without torsion or adhesive |
US5896634A (en) * | 1996-01-13 | 1999-04-27 | Akzo Nobel Nv | Sizing agent-free tangled multifilament yarn and process for its manufacture |
JP2002194658A (en) * | 2000-12-25 | 2002-07-10 | Toray Ind Inc | Method for sizing aliphatic polyester yarn and method for producing woven fabric |
KR100431253B1 (en) * | 2001-09-17 | 2004-05-12 | 김진한 | Method for manufacturing textile using residue yarn |
-
1990
- 1990-10-25 JP JP28580590A patent/JPH04163336A/en active Pending
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2720413A1 (en) * | 1994-05-27 | 1995-12-01 | Rhone Poulenc Fibres | Multifilament polyester thread for weaving without torsion or adhesive |
WO1995033089A1 (en) * | 1994-05-27 | 1995-12-07 | Rhone-Poulenc Setila | Interwoven polyester yarn for weaving without sizing |
US5896634A (en) * | 1996-01-13 | 1999-04-27 | Akzo Nobel Nv | Sizing agent-free tangled multifilament yarn and process for its manufacture |
JP2002194658A (en) * | 2000-12-25 | 2002-07-10 | Toray Ind Inc | Method for sizing aliphatic polyester yarn and method for producing woven fabric |
KR100431253B1 (en) * | 2001-09-17 | 2004-05-12 | 김진한 | Method for manufacturing textile using residue yarn |
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