JPS6144976B2 - - Google Patents
Info
- Publication number
- JPS6144976B2 JPS6144976B2 JP4469582A JP4469582A JPS6144976B2 JP S6144976 B2 JPS6144976 B2 JP S6144976B2 JP 4469582 A JP4469582 A JP 4469582A JP 4469582 A JP4469582 A JP 4469582A JP S6144976 B2 JPS6144976 B2 JP S6144976B2
- Authority
- JP
- Japan
- Prior art keywords
- yarn
- acid
- processed
- multifilament yarn
- undrawn multifilament
- 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.)
- Expired
Links
- 229920000728 polyester Polymers 0.000 claims description 21
- 239000003795 chemical substances by application Substances 0.000 claims description 17
- 238000000034 method Methods 0.000 claims description 17
- 230000001070 adhesive effect Effects 0.000 claims description 15
- 239000000853 adhesive Substances 0.000 claims description 14
- 239000012209 synthetic fiber Substances 0.000 claims description 7
- 229920002994 synthetic fiber Polymers 0.000 claims description 7
- 229920001169 thermoplastic Polymers 0.000 claims description 6
- 239000004416 thermosoftening plastic Substances 0.000 claims description 6
- 238000013019 agitation Methods 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 2
- -1 alkylene glycols Chemical class 0.000 description 13
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 13
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 8
- 238000012546 transfer Methods 0.000 description 7
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 6
- 239000000835 fiber Substances 0.000 description 6
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 6
- 239000002253 acid Substances 0.000 description 5
- 239000001257 hydrogen Substances 0.000 description 5
- 229910052739 hydrogen Inorganic materials 0.000 description 5
- 238000012545 processing Methods 0.000 description 5
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 4
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- 239000002202 Polyethylene glycol Substances 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- VEIOBOXBGYWJIT-UHFFFAOYSA-N cyclohexane;methanol Chemical compound OC.OC.C1CCCCC1 VEIOBOXBGYWJIT-UHFFFAOYSA-N 0.000 description 3
- 239000003292 glue Substances 0.000 description 3
- 238000003754 machining Methods 0.000 description 3
- 229920001515 polyalkylene glycol Polymers 0.000 description 3
- 229920001223 polyethylene glycol Polymers 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-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
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- FQORROGUIFBEFC-UHFFFAOYSA-N OC(=O)C1=CC([Na])=CC(C(O)=O)=C1S(O)(=O)=O Chemical compound OC(=O)C1=CC([Na])=CC(C(O)=O)=C1S(O)(=O)=O FQORROGUIFBEFC-UHFFFAOYSA-N 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 125000002029 aromatic hydrocarbon group Chemical group 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- QYQADNCHXSEGJT-UHFFFAOYSA-N cyclohexane-1,1-dicarboxylate;hydron Chemical compound OC(=O)C1(C(O)=O)CCCCC1 QYQADNCHXSEGJT-UHFFFAOYSA-N 0.000 description 2
- YZFOGXKZTWZVFN-UHFFFAOYSA-N cyclopentane-1,1-dicarboxylic acid Chemical compound OC(=O)C1(C(O)=O)CCCC1 YZFOGXKZTWZVFN-UHFFFAOYSA-N 0.000 description 2
- WOZVHXUHUFLZGK-UHFFFAOYSA-N dimethyl terephthalate Chemical compound COC(=O)C1=CC=C(C(=O)OC)C=C1 WOZVHXUHUFLZGK-UHFFFAOYSA-N 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000004043 dyeing Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 150000002431 hydrogen Chemical group 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229910021645 metal ion Inorganic materials 0.000 description 2
- 239000003595 mist Substances 0.000 description 2
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 2
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 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
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- 238000009987 spinning Methods 0.000 description 2
- 238000010186 staining Methods 0.000 description 2
- 238000012360 testing method Methods 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
- RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 description 1
- MQCPOLNSJCWPGT-UHFFFAOYSA-N 2,2'-Bisphenol F Chemical compound OC1=CC=CC=C1CC1=CC=CC=C1O MQCPOLNSJCWPGT-UHFFFAOYSA-N 0.000 description 1
- GBURUDXSBYGPBL-UHFFFAOYSA-N 2,2,3-trimethylhexanedioic acid Chemical compound OC(=O)C(C)(C)C(C)CCC(O)=O GBURUDXSBYGPBL-UHFFFAOYSA-N 0.000 description 1
- FQXGHZNSUOHCLO-UHFFFAOYSA-N 2,2,4,4-tetramethyl-1,3-cyclobutanediol Chemical compound CC1(C)C(O)C(C)(C)C1O FQXGHZNSUOHCLO-UHFFFAOYSA-N 0.000 description 1
- MQXNNWDXHFBFEB-UHFFFAOYSA-N 2,2-bis(2-hydroxyphenyl)propane Chemical compound C=1C=CC=C(O)C=1C(C)(C)C1=CC=CC=C1O MQXNNWDXHFBFEB-UHFFFAOYSA-N 0.000 description 1
- BTUDGPVTCYNYLK-UHFFFAOYSA-N 2,2-dimethylglutaric acid Chemical compound OC(=O)C(C)(C)CCC(O)=O BTUDGPVTCYNYLK-UHFFFAOYSA-N 0.000 description 1
- DTDASAMIKDAZJX-UHFFFAOYSA-N 2,6-dichloro-3-[2-(2,4-dichloro-3-hydroxyphenyl)propan-2-yl]phenol Chemical compound C=1C=C(Cl)C(O)=C(Cl)C=1C(C)(C)C1=CC=C(Cl)C(O)=C1Cl DTDASAMIKDAZJX-UHFFFAOYSA-N 0.000 description 1
- AOFRNZNXMCOXHP-UHFFFAOYSA-N 2-(2-carboxyphenyl)sulfonylbenzoic acid Chemical compound OC(=O)C1=CC=CC=C1S(=O)(=O)C1=CC=CC=C1C(O)=O AOFRNZNXMCOXHP-UHFFFAOYSA-N 0.000 description 1
- BLDLRWQLBOJPEB-UHFFFAOYSA-N 2-(2-hydroxyphenyl)sulfanylphenol Chemical compound OC1=CC=CC=C1SC1=CC=CC=C1O BLDLRWQLBOJPEB-UHFFFAOYSA-N 0.000 description 1
- WRFLIILFPBSTQD-UHFFFAOYSA-N 2-(2-methylpropyl)pentane-1,3-diol Chemical compound CCC(O)C(CO)CC(C)C WRFLIILFPBSTQD-UHFFFAOYSA-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
- PYPNUHUCANJSEP-UHFFFAOYSA-N 2-[3-(2-hydroxyphenyl)-3-bicyclo[2.2.1]heptanyl]phenol Chemical compound OC1=CC=CC=C1C1(C=2C(=CC=CC=2)O)C(C2)CCC2C1 PYPNUHUCANJSEP-UHFFFAOYSA-N 0.000 description 1
- BGJPCIFNQHHMFU-UHFFFAOYSA-N 2-butylpentane-1,3-diol Chemical compound CCCCC(CO)C(O)CC BGJPCIFNQHHMFU-UHFFFAOYSA-N 0.000 description 1
- YZTJKOLMWJNVFH-UHFFFAOYSA-N 2-sulfobenzene-1,3-dicarboxylic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1S(O)(=O)=O YZTJKOLMWJNVFH-UHFFFAOYSA-N 0.000 description 1
- RAADBCJYJHQQBI-UHFFFAOYSA-N 2-sulfoterephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C(S(O)(=O)=O)=C1 RAADBCJYJHQQBI-UHFFFAOYSA-N 0.000 description 1
- ODJQKYXPKWQWNK-UHFFFAOYSA-N 3,3'-Thiobispropanoic acid Chemical compound OC(=O)CCSCCC(O)=O ODJQKYXPKWQWNK-UHFFFAOYSA-N 0.000 description 1
- RGUZWBOJHNWZOK-UHFFFAOYSA-N 3,6-dimethylbenzene-1,2-diol Chemical compound CC1=CC=C(C)C(O)=C1O RGUZWBOJHNWZOK-UHFFFAOYSA-N 0.000 description 1
- BQZOAXZLOCOWMI-UHFFFAOYSA-N 3-(2-hydroxyphenyl)benzene-1,2,4-triol Chemical compound OC1=CC=C(O)C(C=2C(=CC=CC=2)O)=C1O BQZOAXZLOCOWMI-UHFFFAOYSA-N 0.000 description 1
- KYSWVYKOENHLIQ-UHFFFAOYSA-N 3-ethyl-2-methylheptane-2,4-diol Chemical compound CCCC(O)C(CC)C(C)(C)O KYSWVYKOENHLIQ-UHFFFAOYSA-N 0.000 description 1
- SDGNNLQZAPXALR-UHFFFAOYSA-N 3-sulfophthalic acid Chemical compound OC(=O)C1=CC=CC(S(O)(=O)=O)=C1C(O)=O SDGNNLQZAPXALR-UHFFFAOYSA-N 0.000 description 1
- HBLRZDACQHNPJT-UHFFFAOYSA-N 4-sulfonaphthalene-2,7-dicarboxylic acid Chemical compound OS(=O)(=O)C1=CC(C(O)=O)=CC2=CC(C(=O)O)=CC=C21 HBLRZDACQHNPJT-UHFFFAOYSA-N 0.000 description 1
- BGQNNKZAJXZSPQ-UHFFFAOYSA-N 5,6-dimethylheptane-1,6-diol Chemical compound CC(O)(C)C(C)CCCCO BGQNNKZAJXZSPQ-UHFFFAOYSA-N 0.000 description 1
- QEVGZEDELICMKH-UHFFFAOYSA-N Diglycolic acid Chemical compound OC(=O)COCC(O)=O QEVGZEDELICMKH-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 206010067482 No adverse event Diseases 0.000 description 1
- ALQSHHUCVQOPAS-UHFFFAOYSA-N Pentane-1,5-diol Chemical compound OCCCCCO ALQSHHUCVQOPAS-UHFFFAOYSA-N 0.000 description 1
- CXOFVDLJLONNDW-UHFFFAOYSA-N Phenytoin Chemical group N1C(=O)NC(=O)C1(C=1C=CC=CC=1)C1=CC=CC=C1 CXOFVDLJLONNDW-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- 239000003490 Thiodipropionic acid Substances 0.000 description 1
- 230000002159 abnormal effect Effects 0.000 description 1
- 230000005856 abnormality Effects 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- KYQRDNYMKKJUTH-UHFFFAOYSA-N bicyclo[2.2.1]heptane-3,4-dicarboxylic acid Chemical compound C1CC2(C(O)=O)C(C(=O)O)CC1C2 KYQRDNYMKKJUTH-UHFFFAOYSA-N 0.000 description 1
- 230000001588 bifunctional effect Effects 0.000 description 1
- 239000001273 butane Substances 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
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- OREAFAJWWJHCOT-UHFFFAOYSA-N dimethylmalonic acid Chemical compound OC(=O)C(C)(C)C(O)=O OREAFAJWWJHCOT-UHFFFAOYSA-N 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- GWZCCUDJHOGOSO-UHFFFAOYSA-N diphenic acid Chemical compound OC(=O)C1=CC=CC=C1C1=CC=CC=C1C(O)=O GWZCCUDJHOGOSO-UHFFFAOYSA-N 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 238000007730 finishing process Methods 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 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
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- KYTZHLUVELPASH-UHFFFAOYSA-N naphthalene-1,2-dicarboxylic acid Chemical compound C1=CC=CC2=C(C(O)=O)C(C(=O)O)=CC=C21 KYTZHLUVELPASH-UHFFFAOYSA-N 0.000 description 1
- NXPPAOGUKPJVDI-UHFFFAOYSA-N naphthalene-1,2-diol Chemical compound C1=CC=CC2=C(O)C(O)=CC=C21 NXPPAOGUKPJVDI-UHFFFAOYSA-N 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 235000019303 thiodipropionic acid Nutrition 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Landscapes
- Yarns And Mechanical Finishing Of Yarns Or Ropes (AREA)
Description
本発明は、熱可塑性合成繊維未延伸マルチフイ
ラメント糸を延伸すると同時に、仮撚加工して捲
縮加工糸を製造するに際し、先に加工する未延伸
マルチフイラメント糸の後端部と次に加工する未
延伸マルチフイラメント糸の先端部とを接続する
ことにより、連続的に延伸同時仮撚加工を実施
し、効果的に捲縮加工糸を製造する方法に関す
る。
ポリエステル未延伸糸を延伸と同時に仮撚加工
して捲縮加工糸を製造するに際し、加工中(仕掛
中)のパツケージにおける未延伸マルチフイラメ
ント糸の後端部と次に加工すべきパツケージにお
ける未延伸マルチフイラメント糸の先端部とを結
び合わせる所謂テール・トランスフアーによつて
パツケージ交換時の糸掛け操作を省略して連続的
に延伸同時仮撚加工を行なうことはよく知られて
おり、糸接続の方法としては、種々の糸結び方
法、あるいは空気撹乱流を施して互いに交絡せし
める方法が知られている。
しかしながら、このような方法では、以下の欠
点を有し、加工速度700m/分以上の高速加工に
は、採用が不可能である。
すなわち、糸結びの方法では、結び部分の強度
は、十分に期待し得る結果を得られるが、糸の結
び目が、外装式摩擦仮撚加工装置を通過するとき
に、延伸張力が変化し、その結果延伸点の変動を
まねき、染斑の発生および捲縮異常をもたらすと
いう欠点が生じ、採用は不可能である。
一方、空気撹乱流処理を施して、先に加工する
未延伸マルチフイラメント糸の後端部と次に加工
する未延伸マルチフイラメント糸の先端部を互い
に交絡せしめることで、両マルチフイラメントを
接続する方法によれば、染斑、捲縮異常の発生は
なく、品質面は良好であるものの、接続部の強度
が小さく、また、強度にばらつきが多いため、高
速加工に耐え得るには不十分で、テール・トラン
スフアー時に接続部の抜けが発生し、断糸に到る
問題が顕在化している。
本発明者らは、従来の糸結び方法および空気撹
乱流処理による糸接続方法で糸を接続し、未延伸
マルチフイラメント糸をテール・トランスフアー
する場合の上述の如き欠点を解消すべく研究の結
果、先に加工する未延伸マルチフイラメント糸の
後端部と次に加工する未延伸マルチフイラメント
糸の先端部を、空気撹乱流処理を施して接続した
後、該接続部分に接着処理剤を付与することで、
高速加工においても、品質面における問題もな
く、接続部の強度を格段に改善できるばかりか、
該接続部前後の集束性を向上できることを見い出
し本発明に到達した。
すなわち、本発明は、熱可塑性合成繊維未延伸
マルチフイラメント糸を延伸と同時に仮撚加工し
て、捲縮加工糸を製造するにあたり、先に加工す
る未延伸マルチフイラメント糸の後端部と次に加
工する未延伸マルチフイラメント糸の先端部とを
空気撹乱流処理により互いに交絡せしめた後、そ
の交絡部に接着処理剤を付与し、該両端部を接続
することにより、連続的に延伸同時仮撚加工を行
なうことを特徴とするポリエステル捲縮加工糸の
製造法である。
本発明方法が適用される熱可塑性合成繊維とし
ては、ポリエステル繊維、ポリアミド繊維等延伸
同時仮撚加工が可能なすべての熱可塑性合成繊維
をあげることができる。
また、本発明方法において使用する接着処理剤
としては、通常、繊維用糊剤として知られている
処理剤を、広く用いることができるが、中でも水
溶性ポリエステルが特に好適である。水溶性ポリ
エステルは、簡単な水洗処理によつて極めて容易
に除去することができ、しかも合成繊維としてポ
リエステル繊維を用いた場合は特に強固な接着力
が得られる。
水溶性ポリエステルは、ジカルボン酸、アルキ
レングリコール並びにSO3M基(Mは水素又は金
属イオン)を有する二官能性化合物及び/又はポ
リアルキレングリコールからなつている。
ジカルボン酸成分は、芳香族、脂肪族、脂環族
ジカルボン酸であり、蓚酸、マロン酸、ジメチル
マロン酸、コハク酸、グルタール酸、アジピン
酸、トリメチルアジピン酸、ピメリン酸、2.2ジ
メチルグルタール酸、アゼライン酸、セバシン
酸、フマール酸、マレイン酸、イタコン酸、1.3
シクロペンタンジカルボン酸、1.2シクロヘキサ
ンジカルボン酸、1.3シクロペンタンジカルボン
酸、1.4シクロヘキサンジカルボン酸、フタール
酸、テレフタール酸、イソフタール酸、2.5ノル
ボルナンジカルボン酸、1.4ナフタール酸ジフエ
ニン酸、4.4′オキシ安息香酸、ジグリコール酸、
チオジプロピオン酸、4.4′スルホニルジ安息香酸
及び2.5ナフタレンジカルボン酸があり、この中
でもテレフタール酸、イソフタール酸が望まし
い。
アルキレングリコール成分としては、エチレン
グリコール、プロピレングリコール、ジエチレン
グリコール、2.4ジメチル2エチルヘキサン1.3ジ
オール、2エチル2ブチル1.3プロパンジオー
ル、2.2ジメチル1.3プロパンジオール、2エチル
2イソブチル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、1.5ペンタンジオー
ル、1.6ヘキサンジオール、2.2.4トリメチル1.6ヘ
キサンジオール、1.2シクロヘキサンジメタノー
ル、1.3シクロヘキサンジメタノール、1.4シクロ
ヘキサンジメタノール、2.2.4.4テトラメチル1.3
シクロブタンジオール、4.4′チオジフエノール、
4.4′メチレンジフエノール、4.4′(2・ノルボル
ニリデン)ジフエノール、4.4′ジヒドロキシビフ
エノール、o−,m−及びp−ジヒドロキシベン
ゼン、4.4′イソプロピリデンジフエノール、4.4イ
ソプロピリデンビス(2.6ジクロロフエノール)、
2.5ナフタレンジオール及びp−キシレンジオー
ル等があげられ、この中でもエチレングリコー
ル、ジエチレングリコールが好ましい。
ポリアルキレングリコール成分としては、ポリ
エチレングリコール、ポリプロピレングリコール
等があげられる。
ポリアルキレングリコールの役割は繊維と水溶
性ポリエステルとの結合を強固ならしめると共
に、水溶性ポリエステルに柔かさを与えるもので
ある。
−SO3M基(Mは水素又は金属イオン)を有す
る二官能性化合物成分としては、−SO3M基含有
ジカルボン酸ジオール、オキシ酸がある。
MとしてはLi+,Na+,K+,Mg++,Ca++,
Cu++,Fe++又はFe+++等があり、Na+,Li+が好
ましい。
化合物としては、−SO3M基が芳香族核に直結
したもので、一般式
(Xは3価の芳香族炭化水素基、
Yは2価の芳香族炭化水素基、
Rは水素、又は炭素1〜4のアルキル基、
Mは水素、Li+,Na+,K+,Mg++,Ca++,
Cu++,Fe++又はFe+++、
aは1,2又は3である。)
(Rは水素、炭素数1〜8のアルキル基又はフエ
ニル基,
MはNa+,Li+,K+,Mg++,Ca++,Cu++,
Fe++又はFe+++、
aは1,2又は3である。)
で示される化合物があげられ、具体的にはスルホ
イソフタール酸、スルホテレフタール酸、スルホ
フタール酸又は4−スルホナフタレン2.7ジカル
ボン酸等の金属塩、4−ソジオスルホフエニル−
3−5−ジカルボメトキシベンゼンスルホネー
ト、4−リチオスルホフエニール3.5−ジカルボ
メトキシベンゼンスルホネート及び6−ソジオス
ルホ−2−ナフチル3.5ジカルボメトキシベンゼ
ンスルホネート、5−〔4−(ソジオスルホ)−フ
エノキシ〕イソフタール酸ジメチル、5.〔(ソジ
オスルホ)・フエノキシ〕テレフタール酸ジメチ
ル及び5.〔4.(ソジオスルホ)・フエノキシ〕イ
ソフタール酸等がある。
このうち、Na金属が結合しているソジオスル
ホイソフタール酸が特に好ましい。これらの組成
及び割合は、得られたポリエステルが水溶性にな
れば特に限定しないが、ソジオスルホイソフター
ル酸20〜40モル%共重合ポリエステルが望まし
い。
得られたポリエステルは極限粘度(IV)が0.15
〜0.5程度で常温では固体で安定なポリマーであ
り、水又は熱水に溶解した場合、透明若しくは懸
濁状態となる。
かかる接着処理剤を先に加工する未延伸マルチ
フイラメント糸の後端部と次に加工する未延伸マ
ルチフイラメント糸の先端部とに空気撹乱流を施
して互いに交絡せしめたテール接続部分に付与す
るわけであるが、その付与方法は接着処理剤の水
溶液を刷毛で塗布しても良いし、またスプレー方
式あるいはウエス等に含浸して塗布してもその効
果は変らない。
更に、空気撹乱流中に接着処理剤をミスト状に
分散させておいて空気撹乱流処理とミスト状の接
着処理剤付与を同時に行なつてもよい。
本発明においては、接着処理剤の付与量は特に
限定されるものでなく、処理剤濃度が1〜2重量
%以上であれば、十分にその目的を達成すること
ができる。
又、該処理部分の乾操についても、特に注意を
払う必要はなく通常行なわれているテール・トラ
ンスフアー接続部通過の3〜5時間前に交絡処理
及び接着処理剤処理を完了していれば良い。
以上説明した如く、本発明によれば、マルチフ
イラメント糸の接続部において、繊維間に強固な
接着効果が生じ、接続部の破断強度が非接続部の
それと同等の値を示すと共に、該接続部前後の集
束性を向上できるので700m/分以上の高速で延
伸同時仮撚加工する場合でも、接続部付近に素抜
け、糸切れ、毛羽の発生はなく、テール・トラン
スフアー時の断糸を大幅に減少することが可能と
なり、断糸による機台の稼動率を低下させること
なく連続加工でき、生産性を飛躍的に向上させる
ことが可能となる。更には接着処理剤に特殊な水
溶性ポリエステルを使用した場合は、処理剤の除
去が極めて容易であり、処理剤が残存して仮撚加
工糸の染色仕上げ工程において染斑等のトラブル
が発生するようなことはまつたくない。
以下、実施例により本発明を更に詳述する。
実施例 1
紡糸速度3500m/分にて紡糸した115デニル/
36フイラメントのポリエチレンテレフタレート未
延伸マルチフイラメント糸同志を空気撹乱流処理
にて交絡接続し、該接続部分に各種濃度の水溶性
ポリエステル、又はアクリル酸エステル糊剤水溶
性を刷毛で塗布し、8時間放置して乾燥、固化さ
せた後、インストロン型引張試験機で試料長5cm
(接続部分を試料の中央に位置させる)、ストレツ
チスピード1000%分の条件にて荷伸曲線を測定
し、該荷伸曲線から切断強力を求めた。水溶性ポ
リエステルとしては、5ソジオスルホイソフター
ル酸20重量部、テレフタル酸80重量部、エチレン
グリコール76重量部、ポリエチレングリコール
(分子量600)5重量部を反応させて得られた極限
粘度0.35のものを、またアクリル酸エステル糊剤
としては互応化学社のサイテツクスJ−6を使用
した。結果を第1表に示す。
また、比較のために、接着処理剤を糸条接続部
に塗布しない試料、及び糸条接続部の存在しない
通常の糸条についても切断強力を測定し、第1表
にあわせて示した。
第1表からも明らかなように水溶性ポリエステ
ルあるいはアクリル酸エステル糊剤を糸条接続部
に塗布した糸の強力は非接続部分と同等の強力を
保持し、該方法が糸条接続部分の強力増に顕著な
効果を発揮することがわかる。
In the present invention, when a thermoplastic synthetic fiber undrawn multifilament yarn is drawn and simultaneously subjected to false twisting to produce a crimped yarn, the trailing end of the undrawn multifilament yarn is processed first and then processed. The present invention relates to a method for effectively producing crimped yarn by continuously performing stretching and simultaneous false twisting by connecting the ends of undrawn multifilament yarns. When polyester undrawn yarn is stretched and simultaneously false twisted to produce crimped yarn, the rear end of the undrawn multifilament yarn in the package cage during processing (in progress) and the unstretched yarn in the package cage to be processed next. It is well known that the so-called tail transfer method, which connects the ends of multifilament yarns, allows continuous drawing and simultaneous false twisting, omitting the yarn threading operation when changing the package cage. As methods, various methods of tying the threads or a method of applying air turbulence to intertwine the threads are known. However, such a method has the following drawbacks and cannot be used for high-speed machining at a machining speed of 700 m/min or more. In other words, with the yarn knotting method, the strength of the knotted part can be expected to be sufficiently high, but when the yarn knot passes through the external friction false twisting device, the stretching tension changes and the As a result, it has the drawbacks of causing fluctuations in the drawing point, causing staining spots and abnormal crimp, and cannot be adopted. On the other hand, a method of connecting both multifilaments by applying air turbulence treatment to intertwine the rear end of the undrawn multifilament yarn to be processed first and the tip of the undrawn multifilament yarn to be processed next. According to the company, although the quality is good with no staining spots or crimp abnormalities, the strength of the joints is low and there are many variations in strength, so it is insufficient to withstand high-speed processing. Problems such as disconnection of the connection part during tail transfer and thread breakage have become apparent. The present inventors have conducted research to solve the above-mentioned drawbacks when tail transferring undrawn multifilament yarn by connecting yarns using the conventional yarn tying method and the yarn connecting method using air turbulence treatment. After connecting the rear end of the undrawn multifilament yarn to be processed first and the tip of the undrawn multifilament yarn to be processed next by applying air turbulence treatment, an adhesive treatment agent is applied to the connection part. By that,
Even in high-speed machining, there are no quality problems, and the strength of the connection part can be significantly improved.
The present invention was achieved by discovering that the convergence before and after the connecting portion can be improved. That is, in the present invention, when a thermoplastic synthetic fiber undrawn multifilament yarn is stretched and simultaneously false twisted to produce a crimped yarn, the trailing end of the undrawn multifilament yarn to be processed first and the rear end of the undrawn multifilament yarn processed first and then After the tips of the undrawn multifilament yarn to be processed are entangled with each other by air turbulence treatment, an adhesive treatment agent is applied to the entangled portion and both ends are connected, thereby allowing continuous drawing and simultaneous false twisting. This is a method for producing crimped polyester yarn, which is characterized by carrying out processing. Thermoplastic synthetic fibers to which the method of the present invention can be applied include all thermoplastic synthetic fibers that can be simultaneously stretched and false-twisted, such as polyester fibers and polyamide fibers. Furthermore, as the adhesive treatment agent used in the method of the present invention, a wide variety of treatment agents that are generally known as fiber sizing agents can be used, but water-soluble polyester is particularly suitable. Water-soluble polyester can be removed very easily by a simple water washing treatment, and particularly strong adhesive strength can be obtained when polyester fiber is used as the synthetic fiber. Water-soluble polyesters consist of dicarboxylic acids, alkylene glycols and difunctional compounds having SO 3 M groups (M being hydrogen or a metal ion) and/or polyalkylene glycols. Dicarboxylic acid components are aromatic, aliphatic, and alicyclic dicarboxylic acids, including oxalic acid, malonic acid, dimethylmalonic acid, succinic acid, glutaric acid, adipic acid, trimethyladipic acid, pimelic acid, 2.2 dimethylglutaric acid, Azelaic acid, sebacic acid, fumaric acid, maleic acid, itaconic acid, 1.3
Cyclopentanedicarboxylic acid, 1.2 cyclohexanedicarboxylic acid, 1.3 cyclopentanedicarboxylic acid, 1.4 cyclohexanedicarboxylic acid, phthalic acid, terephthalic acid, isophthalic acid, 2.5 norbornanedicarboxylic acid, 1.4naphthalic acid, diphenic acid, 4.4′ oxybenzoic acid, diglycolic acid ,
Examples include thiodipropionic acid, 4.4'sulfonyl dibenzoic acid and 2.5 naphthalenedicarboxylic acid, and among these, terephthalic acid and isophthalic acid are preferred. The alkylene glycol components include ethylene glycol, propylene glycol, diethylene glycol, 2.4 dimethyl 2 ethylhexane 1.3 diol, 2 ethyl 2 butyl 1.3 propane diol, 2.2 dimethyl 1.3 propane diol, 2 ethyl 2 isobutyl 1.3 propane diol, 1.3 butane diol, 1.4 butane. Diol, 1.5 Pentanediol, 1.6 Hexanediol, 2.2.4 Trimethyl 1.6 Hexanediol, 1.2 Cyclohexane dimethanol, 1.3 Cyclohexane dimethanol, 1.4 Cyclohexane dimethanol, 2.2.4.4 Tetramethyl 1.3
Cyclobutanediol, 4.4′thiodiphenol,
4.4′ methylene diphenol, 4.4′ (2-norbornylidene) diphenol, 4.4′ dihydroxybiphenol, o-, m- and p-dihydroxybenzene, 4.4′ isopropylidene diphenol, 4.4 isopropylidene bis(2.6 dichlorophenol),
Examples include 2.5 naphthalene diol and p-xylene diol, among which ethylene glycol and diethylene glycol are preferred. Examples of the polyalkylene glycol component include polyethylene glycol, polypropylene glycol, and the like. The role of polyalkylene glycol is to strengthen the bond between the fibers and the water-soluble polyester, and also to provide flexibility to the water-soluble polyester. Examples of the bifunctional compound component having a -SO3M group (M is hydrogen or a metal ion) include -SO3M group-containing dicarboxylic acid diols and oxyacids. M is Li + , Na + , K + , Mg ++ , Ca ++ ,
Examples include Cu ++ , Fe ++ and Fe +++ , with Na + and Li + being preferred. As a compound, the −SO 3 M group is directly connected to an aromatic nucleus, and the general formula is (X is a trivalent aromatic hydrocarbon group, Y is a divalent aromatic hydrocarbon group, R is hydrogen or an alkyl group having 1 to 4 carbon atoms, M is hydrogen, Li + , Na + , K + , Mg ++ , Ca ++ ,
Cu ++ , Fe ++ or Fe +++ , a is 1, 2 or 3. ) (R is hydrogen, an alkyl group having 1 to 8 carbon atoms or a phenyl group, M is Na + , Li + , K + , Mg ++ , Ca ++ , Cu ++ ,
Fe ++ or Fe +++ , a is 1, 2 or 3. ), specifically metal salts such as sulfoisophthalic acid, sulfoterephthalic acid, sulfophthalic acid or 4-sulfonaphthalene 2.7 dicarboxylic acid, 4-sodiosulfophenyl-
3-5-dicarbomethoxybenzenesulfonate, 4-lithiosulfophenyl 3.5-dicarbomethoxybenzenesulfonate and 6-sodiosulfo-2-naphthyl 3.5-dicarbomethoxybenzenesulfonate, 5-[4-(sodiosulfo)-phenoxy]isophthal dimethyl acid, 5. [(sodiosulfo) phenoxy] dimethyl terephthalate, and 5. [4. (sodiosulfo) phenoxy] isophthalic acid. Among these, sodiosulfoisophthalic acid to which Na metal is bonded is particularly preferred. The composition and ratio of these are not particularly limited as long as the obtained polyester is water-soluble, but a copolymerized polyester of 20 to 40 mol% of sodiosulfoisophthalic acid is desirable. The resulting polyester has an intrinsic viscosity (IV) of 0.15
~0.5, it is a solid and stable polymer at room temperature, and when dissolved in water or hot water, it becomes transparent or in a suspended state. The adhesive treatment agent is applied to the tail connecting portion where the trailing end of the undrawn multifilament yarn to be processed first and the tip of the undrawn multifilament yarn to be processed next are intertwined with each other by applying air turbulence to the rear end. However, the application method may be by applying an aqueous solution of the adhesive treatment agent with a brush, or by a spray method or by impregnating a cloth or the like with the application, the effect remains the same. Furthermore, the adhesive treatment agent may be dispersed in the form of a mist in the air turbulent flow, and the air turbulence treatment and the application of the adhesive treatment agent in the form of a mist may be performed simultaneously. In the present invention, the amount of adhesive treatment agent applied is not particularly limited, and as long as the concentration of the treatment agent is 1 to 2% by weight or more, the purpose can be sufficiently achieved. Also, there is no need to pay special attention to the drying of the treated area, as long as the entanglement treatment and adhesive treatment are completed 3 to 5 hours before passing through the tail transfer connection area, which is normally done. good. As explained above, according to the present invention, a strong adhesive effect occurs between the fibers at the joints of multifilament yarns, the breaking strength of the joints shows a value equivalent to that of the unconnected parts, and the joints Because the front and back convergence can be improved, even when drawing and simultaneously false-twisting is performed at high speeds of 700 m/min or higher, there is no looseness, yarn breakage, or fluffing near the joint, and yarn breakage during tail transfer is greatly reduced. This makes it possible to perform continuous processing without reducing the operating rate of the machine due to yarn breakage, and it becomes possible to dramatically improve productivity. Furthermore, when special water-soluble polyester is used as an adhesive treatment agent, it is extremely easy to remove the treatment agent, and the treatment agent remains, causing problems such as dyeing spots during the dyeing and finishing process of false twisted yarn. I don't want something like that to happen. Hereinafter, the present invention will be explained in further detail with reference to Examples. Example 1 115 denyl/spun at a spinning speed of 3500 m/min
36-filament polyethylene terephthalate undrawn multifilament yarns were interlaced and connected together using air agitation and turbulence treatment, and various concentrations of water-soluble polyester or water-soluble acrylic ester glue were applied to the connected parts with a brush and left for 8 hours. After drying and solidifying, test the specimen with a length of 5 cm using an Instron tensile tester.
The stretching curve was measured under the conditions of 1000% stretching speed (with the connecting portion located at the center of the sample), and the cutting strength was determined from the stretching curve. The water-soluble polyester has an intrinsic viscosity of 0.35 and is obtained by reacting 20 parts by weight of 5-sodiosulfoisophthalic acid, 80 parts by weight of terephthalic acid, 76 parts by weight of ethylene glycol, and 5 parts by weight of polyethylene glycol (molecular weight 600). and, as the acrylic ester glue, Cytecs J-6 manufactured by Gooh Kagaku Co., Ltd. was used. The results are shown in Table 1. For comparison, the cutting strength was also measured for samples in which no adhesive treatment agent was applied to the yarn joints, and for ordinary yarns without yarn joints, and the results are also shown in Table 1. As is clear from Table 1, the strength of the yarn coated with water-soluble polyester or acrylic ester glue at the yarn joints remains the same as that of the non-connected parts, and this method is effective in increasing the strength of the yarn joints. It can be seen that it has a remarkable effect on increase.
【表】
実施例 2
紡糸速度3500m/分により溶融紡糸した115デ
ニール/36フイラメント10Kg捲のポリエチレンテ
レフタレート未延伸マルチフイラメント糸パツケ
ージを外接式摩擦仮撚加工装置を備えた延伸同時
仮撚加工機に供給し、延伸と同時に仮撚加工を実
施した。
仮撚機はスクラツグ社のスーパードローセツト
8型を用いて、仮撚速度700m/分、延伸倍率
1.52倍、第1ヒーター温度220℃にて5Kg捲パツ
ケージに加工した。この際、先に加工する未延伸
糸パツケージの糸条後端部と次に加工する未延伸
糸パツケージの糸条先端部とを引揃えて圧空圧力
5Kg/cm2の空気撹乱流処理を施し、両糸条の構成
フイラメントを互いに交絡せしめて接続した後、
該接続部分に各種濃度の水溶性ポリエステルを刷
毛にて塗布した。
水溶性ポリエステルとしては5ソジオスルホイ
ソフタール酸20重量部、テレフタル酸80重量部、
エチレングリコール76重量部、ポリエチレングリ
コール(分子量600)5重量部を反応させて得ら
れた極限粘度0.35のものを用いた。一方、比較の
ために、接続部に水溶性ポリエステルを塗布しな
いものについても同様のテストを行なつた。該糸
条のテール・トランスフアー通過性及び捲縮加工
糸の品質を第2表に示す。尚、各実験における加
工総量はそれぞれ10.8トンであつた。[Table] Example 2 A polyethylene terephthalate undrawn multifilament yarn package of 10 kg of 115 denier/36 filaments melt-spun at a spinning speed of 3500 m/min was fed to a drawing and simultaneous false-twisting machine equipped with a circumscribed friction false-twisting device. Then, a false twisting process was carried out simultaneously with the stretching. The false twisting machine used was a Super Draw Set 8 model manufactured by Scruggs Co., Ltd., with a false twisting speed of 700 m/min and a stretching ratio of 700 m/min.
It was processed into a 5 kg package at a temperature of 1.52 times and the first heater temperature of 220°C. At this time, the rear end of the yarn of the undrawn yarn package to be processed first and the tip of the yarn of the undrawn yarn package to be processed next are aligned and subjected to air agitation turbulence treatment at a compressed air pressure of 5 kg/cm 2 , After intertwining and connecting the constituent filaments of both yarns,
Various concentrations of water-soluble polyester were applied to the connection portion using a brush. As the water-soluble polyester, 20 parts by weight of 5-sodiosulfoisophthalic acid, 80 parts by weight of terephthalic acid,
A product with an intrinsic viscosity of 0.35 obtained by reacting 76 parts by weight of ethylene glycol and 5 parts by weight of polyethylene glycol (molecular weight 600) was used. On the other hand, for comparison, a similar test was conducted on a product in which water-soluble polyester was not applied to the connection portion. Table 2 shows the tail transfer permeability of the yarn and the quality of the crimped yarn. The total amount processed in each experiment was 10.8 tons.
【表】
上記から明らかな如く、水溶性ポリエステルを
塗布した糸条のテール・トランスフアー通過性は
極めて良好であり、接続部分の品質にも何らの悪
影響は認められないことがわかる。
尚、テール・トランスフアー通過率とは、先に
加工する未延伸マルチフイラメント糸の後端部と
次に加工する未延伸マルチフイラメント糸の先端
部とを接続した部分が延伸同時仮撚加工装置を通
過する際に切断することなく、無事、通過した割
合を百分率で示したものである。[Table] As is clear from the above, the tail transfer performance of the yarn coated with water-soluble polyester is extremely good, and no adverse effects are observed on the quality of the connected portion. The tail transfer passage rate is defined as the point where the trailing end of the undrawn multifilament yarn to be processed first and the tip of the undrawn multifilament yarn to be processed next pass through the drawing and simultaneous false twisting processing device. This is the percentage of items that successfully passed without being cut during the passage.
Claims (1)
糸を延伸と同時に仮撚加工して、捲縮加工糸を製
造するにあたり、先に加工する未延伸マルチフイ
ラメント糸の後端部と次に加工する未延伸マルチ
フイラメント糸の先端部とを空気撹乱流処理によ
り、互いに交絡せしめた後、その交絡部に接着処
理剤を付与し、該両端部を接続することにより、
連続的に延伸同時仮撚加工を行なうことを特徴と
する熱可塑性合成繊維捲縮加工糸の製造方法。 2 交絡処理部に付与する接着処理剤が水溶性ポ
リエステルである特許請求の範囲第1項記載の方
法。[Claims] 1. When a thermoplastic synthetic fiber undrawn multifilament yarn is stretched and simultaneously false twisted to produce a crimped yarn, the trailing end of the undrawn multifilament yarn processed first and the second By intertwining the tip of the undrawn multifilament yarn to be processed with each other by air agitation turbulence treatment, applying an adhesive treatment agent to the intertwined part and connecting the two ends,
1. A method for producing a crimped thermoplastic synthetic fiber yarn, which comprises continuous stretching and simultaneous false twisting. 2. The method according to claim 1, wherein the adhesive treatment agent applied to the entangled portion is water-soluble polyester.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4469582A JPS58163737A (en) | 1982-03-23 | 1982-03-23 | Production of thermoplastic synthetic fiber crimp processed yarn |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4469582A JPS58163737A (en) | 1982-03-23 | 1982-03-23 | Production of thermoplastic synthetic fiber crimp processed yarn |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS58163737A JPS58163737A (en) | 1983-09-28 |
| JPS6144976B2 true JPS6144976B2 (en) | 1986-10-06 |
Family
ID=12698550
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP4469582A Granted JPS58163737A (en) | 1982-03-23 | 1982-03-23 | Production of thermoplastic synthetic fiber crimp processed yarn |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS58163737A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6438073U (en) * | 1987-09-02 | 1989-03-07 |
-
1982
- 1982-03-23 JP JP4469582A patent/JPS58163737A/en active Granted
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6438073U (en) * | 1987-09-02 | 1989-03-07 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS58163737A (en) | 1983-09-28 |
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