JPS6247989B2 - - Google Patents
Info
- Publication number
- JPS6247989B2 JPS6247989B2 JP6090682A JP6090682A JPS6247989B2 JP S6247989 B2 JPS6247989 B2 JP S6247989B2 JP 6090682 A JP6090682 A JP 6090682A JP 6090682 A JP6090682 A JP 6090682A JP S6247989 B2 JPS6247989 B2 JP S6247989B2
- Authority
- JP
- Japan
- Prior art keywords
- component
- weight
- yarn
- spinning
- metal
- 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
- 229910052751 metal Inorganic materials 0.000 claims description 37
- 239000002184 metal Substances 0.000 claims description 37
- 238000009987 spinning Methods 0.000 claims description 34
- -1 alkyl phosphates Chemical class 0.000 claims description 18
- 229920001296 polysiloxane Polymers 0.000 claims description 15
- 239000012209 synthetic fiber Substances 0.000 claims description 14
- 229920002994 synthetic fiber Polymers 0.000 claims description 14
- 239000003795 chemical substances by application Substances 0.000 claims description 12
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 11
- 239000001993 wax Substances 0.000 claims description 10
- 239000000203 mixture Substances 0.000 claims description 9
- 229920005604 random copolymer Polymers 0.000 claims description 8
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims description 7
- 229910019142 PO4 Inorganic materials 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 6
- 235000021317 phosphate Nutrition 0.000 claims description 6
- 238000009499 grossing Methods 0.000 claims description 5
- 238000007334 copolymerization reaction Methods 0.000 claims description 4
- 229910052783 alkali metal Inorganic materials 0.000 claims description 3
- 150000008052 alkyl sulfonates Chemical class 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 3
- 229920002164 Polyalkylene glycol copolymer Polymers 0.000 claims description 2
- 239000004480 active ingredient Substances 0.000 claims 1
- 239000003513 alkali Substances 0.000 claims 1
- 238000009941 weaving Methods 0.000 description 29
- 238000000034 method Methods 0.000 description 28
- 239000003921 oil Substances 0.000 description 27
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 24
- 238000005299 abrasion Methods 0.000 description 15
- 230000000694 effects Effects 0.000 description 12
- 239000000835 fiber Substances 0.000 description 10
- 229920000570 polyether Polymers 0.000 description 10
- 235000014676 Phragmites communis Nutrition 0.000 description 7
- 244000273256 Phragmites communis Species 0.000 description 6
- 239000003995 emulsifying agent Substances 0.000 description 5
- 150000002148 esters Chemical class 0.000 description 5
- 239000003292 glue Substances 0.000 description 5
- 238000004513 sizing Methods 0.000 description 5
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical group CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
- 239000000839 emulsion Substances 0.000 description 4
- 125000000217 alkyl group Polymers 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000012188 paraffin wax Substances 0.000 description 3
- 235000019809 paraffin wax Nutrition 0.000 description 3
- 235000019271 petrolatum Nutrition 0.000 description 3
- 229920001515 polyalkylene glycol Polymers 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 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 2
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N Propene Chemical group CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 230000002209 hydrophobic effect Effects 0.000 description 2
- 229910052744 lithium Inorganic materials 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 239000002480 mineral oil Substances 0.000 description 2
- 235000010446 mineral oil Nutrition 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- OQILCOQZDHPEAZ-UHFFFAOYSA-N octyl palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OCCCCCCCC OQILCOQZDHPEAZ-UHFFFAOYSA-N 0.000 description 2
- 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 2
- 239000010452 phosphate Substances 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
- 239000005020 polyethylene terephthalate Substances 0.000 description 2
- 230000002265 prevention Effects 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 159000000000 sodium salts Chemical class 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000004018 waxing Methods 0.000 description 2
- YTPNTTUPPCGZPJ-UHFFFAOYSA-N 11-methyldodecyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCCCCCCCCCCC(C)C YTPNTTUPPCGZPJ-UHFFFAOYSA-N 0.000 description 1
- UPLMIMVLCPRUND-UHFFFAOYSA-N 11-methyldodecyl hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCCCCCCCCCCC(C)C UPLMIMVLCPRUND-UHFFFAOYSA-N 0.000 description 1
- SRBSSROHORQGBO-UHFFFAOYSA-N 11-methyldodecyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCCCCCCCCCC(C)C SRBSSROHORQGBO-UHFFFAOYSA-N 0.000 description 1
- 241001589086 Bellapiscis medius Species 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 238000005349 anion exchange Methods 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 235000013871 bee wax Nutrition 0.000 description 1
- 239000012166 beeswax Substances 0.000 description 1
- 150000001555 benzenes Chemical class 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 239000004203 carnauba wax Substances 0.000 description 1
- 235000013869 carnauba wax Nutrition 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- TVACALAUIQMRDF-UHFFFAOYSA-N dodecyl dihydrogen phosphate Chemical compound CCCCCCCCCCCCOP(O)(O)=O TVACALAUIQMRDF-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
- 239000004744 fabric Substances 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 159000000011 group IA salts Chemical class 0.000 description 1
- 238000009998 heat setting Methods 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- 238000002074 melt spinning Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000004200 microcrystalline wax Substances 0.000 description 1
- 235000019808 microcrystalline wax Nutrition 0.000 description 1
- 125000001421 myristyl 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])[H] 0.000 description 1
- BARWIPMJPCRCTP-UHFFFAOYSA-N oleic acid oleyl ester Natural products CCCCCCCCC=CCCCCCCCCOC(=O)CCCCCCCC=CCCCCCCCC BARWIPMJPCRCTP-UHFFFAOYSA-N 0.000 description 1
- 125000001117 oleyl 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])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- BARWIPMJPCRCTP-CLFAGFIQSA-N oleyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCCOC(=O)CCCCCCC\C=C/CCCCCCCC BARWIPMJPCRCTP-CLFAGFIQSA-N 0.000 description 1
- 239000004209 oxidized polyethylene wax Substances 0.000 description 1
- 235000013873 oxidized polyethylene wax Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920006149 polyester-amide block copolymer Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical group [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 239000011253 protective coating Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 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
- 238000003756 stirring Methods 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 125000004417 unsaturated alkyl group Chemical group 0.000 description 1
Landscapes
- Yarns And Mechanical Finishing Of Yarns Or Ropes (AREA)
- Chemical Treatment Of Fibers During Manufacturing Processes (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Description
本発明は合成繊維マルチフイラメントヤーンの
製造法に関する。本発明の目的は、とくに合成繊
維マルチフイラメントを経糸として無糊でウオー
タージエツトルームによつて製織するのに適した
繊維糸条を提供するにある。
従来より合成繊維マルチフイラメントをウオー
タージエツトルームで製織するにさいして、経糸
に用いられる糸条には高度の集束性と適度の平滑
性を付与するため古くは製織工程に先立つて、そ
の準備の工程でいわゆるサイジング剤としての糊
材を付与し、その後アフターワキシングなどを施
し、高度の集束性と適度の平滑性を付与して行な
われていた。この方法は製織安定性が得られるこ
とから現在も尚採用されているが、これと平行し
て昨今はサイジングによる糊付、乾燥、ワキシン
グ工程を省略してウオータージエツトルームによ
つて直接製織しようという一つの試みとして高度
の集束性と適度の平滑性を付与するために紡糸油
剤中にサイジング工程で用いられるような糊材を
配合して行なう方法が数多く提案されている。し
かし、これらの方法では製糸工程における各種ロ
ーラーやガイド類の糸導に相当する部位にスカム
様のものが析出し、そのために毛羽あるいは断糸
の原因になりとくに織物用の細デニール例えば50
デニール/24フイラメントのようなものでは製織
性がきわめて低くなることが知られている。その
ためさらに検討が加えられ、その後ウオータージ
エツトルームによつて製織される経糸に必要な特
性解析から糸/糸間の摩擦による毛羽の発生をで
きるだけおさえるために糸/糸間の摩擦強度を上
げ、かつ集束性を向上させて繊維糸条を構成する
単糸(単繊維)のバラケをできるだけ押える方法
と共に湿時における金属と糸との摩擦を下げて湿
時の潤滑性を向上させることにより毛羽や断糸を
低下させ製織稼働率を向上させるといつた試みが
特開50〜101694号や特開51−47198号公報などで
提案されている。そしてなおその上に高度の集束
性を得るために特公昭36−12230号や特公昭37−
1175号によつて古くから知られているように流体
噴射処理によるマルチフイラメントを構成する単
糸間同志を交絡させるいわばインターレース処理
を紡糸後の製糸工程で施すこともよく知られてい
る。このようにウオータージエツトルームによる
無糊糸の製織性を向上させるという技術の主眼は
製糸工程から製織工程にかけての糸の損傷をでき
るだけ防止して製織効率を高めるための油剤成分
と糸の集束性の技術が組合わされている。確かに
これまで知られているようにウオータージエツト
ルームによる製織稼働率を向上させるために高度
の集束性と適度の平滑性が必要であることは云う
までもないが、ウオータージエツトルームによる
製織性を上げるためにはとくに湿潤時の耐金属摩
耗性が非常に重要である。そこで本発明者らは湿
潤時の単糸毛羽を防止するためというよりは、む
しろもつと積極的に筬や綜絖などの表面をより積
極的に保護し、筬や綜絖の金属表面に保護被膜を
形成させるという考え方からとくに湿時における
油膜強度の強化ということについて検討を重ね
た。その結果繊維糸条の表面保護という面からは
確かに糸と金属の間の動摩擦が低い比較的分子量
の低いエステル類などを多量に含有する組成物で
は一般的には古くからその効果が認められ、ワツ
クス類やシリコン類も夫々同じような効果が認め
られる。しかし、実際の使用に当つてはワツクス
類を多量に使用すれば、延伸ローラー上あるいは
ガイド類にスカム様のものが堆積して糸導を非常
に汚染するばかりでなく、なおその上にウオータ
ージエツトルームによる製織時にも筬、綜絖など
にスカムが固着して製織稼働率を大巾に低下させ
てしまうことが多い。また水不溶性のシリコン類
などを多量に配合すると得られた糸条の染色性を
非常に阻害したり、染色工程で布上にシリコン類
が再付着して実用上問題になる場合が多い。また
一塩基性酸のエステルのように比較的分子量の低
いものを主成分とした場合には繊維と金属の間の
摩擦を低下させて湿時における単糸切れによる毛
羽や糸もつれを改良する面からは好ましい方向で
あるが、これのみでは防止効果にやはり限界があ
ることがわかつた。すなわち金属表面をもつと強
力にかつ積極的に摩耗から保護されることが必要
である。また一般に低分子量のエステル類は耐熱
性が不良で昨今使用し難い場合が多い。逆に耐熱
性を向上させて且つ繊維と金属の摩耗を下げるた
めにエステル系化合物の分子量を上げていく方法
では思つた程繊維と金属間の摩擦の低下は少な
く、なおその上に湿時の耐金属の摩耗性は逆に不
良化した方向にある。
一方、最近繊維の製造においてより生産能率の
向上ということで、より高速化及び高温側での製
糸条件が採用される一方、工程の合理化という面
からは合成繊維糸条を無糊でウオータージエツト
を用い製織することが行なわれてきており、製糸
工程でスカムの発生がきわめて少なく、なおその
上に湿潤時における金属と糸の間の摩耗性を低下
させて単糸毛羽を防ぐといつたことよりも積極的
に湿時の金属表面に保護膜を形成させるといつた
機作の耐金属摩耗性(筬の摩耗防止)のすぐれた
糸条が望まれ、そしてそれに適した紡糸油剤が望
まれている。
本発明者らはかゝる現状に鑑み紡糸及び延伸工
程でのトラブルが少なく、かつウオータージエツ
トルームによる製織時においても耐金属摩耗性に
すぐれた合成繊維糸条を得るべく鋭意検討の結果
紡糸工程において特殊な紡糸油剤配合物を付与
し、かつインターレースを適度にかけることによ
り所期の目的を達成する本発明に到達した。
即ち本発明は公知の平滑剤、乳化剤、集束剤な
どからたる通常の紡糸油剤に対して従来のような
水不溶性の限定された鉱物油がエステル系平滑剤
あるいはワツクス類やシリコン類を用いる方法と
は全く異なつた方法からなるもので、特に、合成
繊維よりなる糸条を未延伸糸の段階で平滑剤及
び/又はポリアルキレングリコールを含む紡糸油
剤を付するにさいし、紡糸油剤の有効成分に対し
てプロピレンオキシドとエチレンオキシドの共重
合比が75/25〜95/5(重量比)で分子量2000〜
15000の水不溶性のランダム共重合体が50%(重
量)を越えて配合され、更に炭素数12〜18のアル
キルホスフエート類のアルカリ金属塩(A成
分)、炭素数12〜18のアルキルスルホネート及
び/又はアルキルサルフエート化合物のアルカリ
塩(B成分)、変性シリコン類(C成分)及びワ
ツクス類(D成分)の4者が必須成分としてA+
B+C+Dの和が4%以上10%以下(重量)でA
+B>C+DでC+Dが少なくとも4%(重量)
以下で配合された組成物を含有する紡糸油剤で表
面処理し、かつ1m当り30ケ以上のランダムに交
絡するようにインターレース処理を施すことを特
徴とする合成繊維マルチフイラメントの製造法か
らなる。該マルチフイラメントヤーンは経糸とし
てウオータージエツトルームで無糊製織性にすぐ
れとくに湿時の金属摩耗を積極的に低下させて製
織稼働率を大巾に向上させることができる。
とくに本発明においてウオータージエツトルー
ムにより無糊での製織性を安定化しかつ稼働率を
向上させるためにはA成分、B成分、C成分そし
てD成分の4者を組合せることが不可欠であり、
これらのいずれが欠けても所期の効果が得られな
いといつた驚くべきシネルギー効果が見出される
ことであり、このシネルギー効果はプロピレンオ
キシドとエチレンオキシドの共合体が75/25〜
95/5(重量比)で分子量が2000〜15000の水不
溶性のランダム共重合体を50%を越えて配合した
紡糸油剤との系でさらに助長するものでかかる事
実はこれまで全く知られていない。すなわちこれ
までに知られてきたような湿時の耐金属摩耗性を
向上させるというエステル系の平滑剤あるいは水
不溶性のワツクス類やシリコン類などとは全く異
なつた機作によるもので糸の表面保護といつたよ
りは、本発明は積極的に金属表面に強力な摩耗防
止膜を形成させようとするものである。もう一つ
重要なことは本発明ではシネルギー効果から各成
分の配合率を夫々最底の範囲におさえながら湿時
の耐金属の摩耗性を向上させるといつたもので、
当然のことながら製糸工程は云うに及ばず製織工
程で無糊でウオータージエツトルームを用いて製
織してもスカム付着などはきわめて少ない。さら
に大きな特徴は平滑剤や乳化剤あるいはポリアル
キレングリコールなどからなる通常公知の紡糸油
剤のいずれでも適用でき、本発明で限定されたプ
ロピレンオキシドとエチレンオキシドの共合比が
75/25〜95/5(重量比)で分子量2000〜15000
の水不溶性のランダム共重合体が全有効成分中で
50%を越える油剤にA、B、C及びDを併用する
ことにより本発明の効果をいちじるしく発現させ
ることができる。さらに本発明者らは特定の紡糸
油剤を付すと共にウオータージエツトルームによ
る製織性を更に向上させるべく検討した所、前記
特定の油剤処理を施した合成繊維マルチフイラメ
ントに特公昭36−12230号、特公昭37−1175号公
報によつて知られているような流体噴射処理によ
つて構成する単糸同志をランダムに交絡させると
いつたインターレース処理を施して合成繊維マル
チフイラメントを製造することにより湿時におけ
る耐金属摩耗防止効果もいちじるしく向上し、製
織時の稼働率も向上しすぐれた製織性を与えるこ
とが判つた。
本発明で用いられる限定されたポリエーテル類
としてはプロピレンオキシドとエチレンオキシド
の共重合比が75/25〜95/5(重量比)の分子量
としては2000〜15000の水不溶性のランダム共重
合体からなり、好ましくは80/20〜90/10のラン
ダム共重合体が望ましい。これらのポリエーテル
は1価あるいは2価さらには多価の活性水素をも
つ化合物(例えば−OH、−COOH、−NH2、−SH
をもつ化合物)に通常公知の方法でエチレンオキ
シド及びプロピレンオキシドをランダム状に付加
して得られるものであり、本発明では疎水性のも
の(水不溶性)が好ましい。水溶性のポリエーテ
ルとして公知のエチレンオキシドの付加モル数の
大きい例えば50/50〜20/80ポリエーテル類で
は、本発明の卓越した効果は極減する。また分子
量が2000未満では優れた耐金属摩耗性を維持する
ことはむずかしいし、15000を越えると耐金属摩
耗性そのものは良好であるが粘度が増大し乾燥時
における繊維の金属に対する摩擦性が大きくなり
すぎ、インターレースノズルに粘着物が付着した
りして製糸安定性が不良になる傾向がある。
次に、A、B、C及びD成分について詳述す
る。A成分は炭素数が12〜18の直鎖あるいは側鎖
の飽和あるいは不飽和のアルキル基を有する通常
公知のアルキルホスフエートのアルカリ金属塩、
例えばナトリウム、カリウム、リチウムなどから
なる。通常マルチフイラメントの制電剤として用
いられるポリオキシエチレン変性のアルキルホス
フエート類は、たとえそのモル数が少ないもの例
えば1モル付加体や2モル付加体でも湿時の耐金
属摩耗という面からは本発明から全く除外され
る。例えばエチレンオキシド1モルが付加した
POE(1)ラウリルホスフエート系のものでも50%
以上含有するものは本発明からは除外されるとい
うきびしい制限がある。本発明で用いられるアル
キルホスフエートの金属塩の中でも好ましくは分
岐のない直鎖のアルキル基がよく、ラウリル、セ
チル、パルミチル、ミリスチル、ステアリル、オ
レイルなどが好ましい。一方A成分に併用される
成分Bは通常公知の炭素数が12〜18からなるアル
キルスルホネートが好ましいが分子内にベンゼン
核のあるスルホネート化合物であつてもよい。そ
の他B成分としてはアルキルサルフエート化合物
あるいは該アルキル基に1〜3モル程度のエチレ
ンオキシドが付加した公知のエチレンオキシド変
性アルキルサルフエート化合物が用いられ、その
塩としてはリチウム、ナトリウムあるいはカリウ
ム塩などがあるが、就中ナトリウム塩が好適に用
いられる。さらにA成分、B成分に併用されるC
成分は変性シリコン類が用いられる。この例とし
ては、フエニル変性シリコン、エポキシ変性シリ
コン、ポリオキシアルキレン変性シリコン、脂肪
酸変性シリコンなどが挙げられるが、これらの変
性シリコン類は通常非イオン活性剤で乳化された
ものが市販で入手可能である。さらにA、B、C
に併用されるD成分としては水不溶性の各種の公
知のワツクス類が用いられるが、例えばパラフイ
ンワツクス、酸化ミクロクリスタリンワツクス、
カルナウバロウ、密ロウ、酸化ポリエチレンワツ
クスなどの天然及び合成ワツクスが挙げられ、な
かでも融点30℃以上〜140℃以下のパラフインワ
ツクスなどが好ましい。これらのワツクス類も通
常非イオン活性剤系の乳化剤によつて水中に分散
したものが入手できるので水性エマルジヨンとし
て適用される。
これらの成分を夫々組合せることによつて本発
明の所期の効果を得るためにはA、B、C及びD
の各成分が常に必須であり、その中の一成分が欠
けても十分その効果を発現できないし、各成分比
のバランスがくずれても最小の添加量で湿時の耐
金属摩耗効果を著しく向上せしめることができな
くなる。もちろん本発明の範囲を越えてA+B+
C+Dの和が10%を越えても湿時の耐金属摩耗の
効果は十分に維持されるが、添加量が多くなると
製糸工程さらにはウオータージエツトルームでの
製織工程でロールやガイドさらには筬や綜絖への
スカムの付着といつたトラブルが増大するので好
ましくない。さらに重要なことはアルキルホスフ
エート類は一般にアニオン交換性があり、とくに
ウオータージエツトルームで製織する場合には水
の硬度が大きくなるとイオン交換性によつて得ら
れる水不溶性のスカムが筬や綜絖に付着して稼働
率低下の直接的な原因となるとも云われている。
したがつて本発明に用いられる配合組成物が筬や
綜絖などの湿時の摩耗に防止効果があるとしても
必要量以上の配合は当然さけるべきで最小量にお
さえることが好ましいことは云うまでもない。し
たがつて本発明においては通常A+B+C+Dの
和に4%以上10%(重量)以下におさえられる。
しかし、A+B>C+Dでアニオン成分は常にワ
ツクス類とシリコン類の和よりも多く、C+Dは
好ましくは4%以下で用いられる。CあるいはD
は通常水不溶成分であるが、適当な乳化剤を用い
て分散することにより通常公知の紡糸油剤中に
4.0%以上でももちろん混合することができる
が、製糸工程や製織工程でのスカムの堆積という
面から好ましくは3.0%以下用いるのがよい。か
くして製糸、製織工程にスカムトラブルなしに湿
潤状態において非常にすぐれた耐金属摩耗防止効
果を発揮することができる。
かかる、湿時における耐金属摩耗防止の組成物
は通常公知の紡糸油剤に配合して用いられ公知の
紡糸油剤を何等限定するものではない。例えば公
知の紡糸油剤として知られている平滑剤及び/又
はポリアルキレングリコール共重合からなる公知
の紡糸油剤さらにくわしくは鉱物油、オクチル−
パルミテート、イソトリデシルラウレート、オレ
イルオレート、イソトリデシル−パルミテート、
イソトリデシルステアレートなどの一塩基性酸の
エステル系化合物を主成分として通常公知の乳化
剤でエマルジヨン化された紡糸油剤及び/又は特
公昭41−13564号公報や英国特許833450号又は米
国特許3338830号明細書に開示されているような
仮撚加工用の油剤としてよく知られているポリア
ルキレングリコール類がエチレンオキシドとプロ
ピレンオキシドが共重合して得られる通常公知の
ポリエーテル類を主体とする紡糸油剤であつても
本発明の組成物を配合することによつて非常にす
ぐれた湿時の耐金属摩耗性を発揮することができ
る。
本発明の対称となる合成繊維としてはポリエス
テル、ポリアミド等の熱可塑性合成繊維よりなり
常法によつて溶融紡糸して得られる合成繊維マル
チフイラメントからなり、特にポリエチレンテレ
フタレート系のポリエステル繊維に好適である。
かゝる合成繊維マルチフイラメントへの本発明
の紡糸油剤の付与方法は溶融紡糸された未延伸糸
に通徐公知のローラーオイリング、スプレーオイ
リングなどによつて付与することができ付着量と
しては0.5〜2.0%(重量)好ましくは0.8〜1.5%
(重量)程度付与させればよい。
以上のようにして本発明は合成繊維マルチフイ
ラメントの製糸工程において紡糸延伸性を何等阻
害することなく、さらに無糊のウオータージエツ
トルームによる製織においても特にすぐれた製織
性を与える経糸用糸条を提供するものである。
次に、本発明の実施例を示すが本発明は何等こ
れに限定されるものではない。又、実施例中の
「部」は重量%を示し、実施例中の湿時の耐金属
摩耗及びインターレースによる絡み度、さらには
製織性については次の方法で測定評価した。
湿潤時の耐金属摩耗性の測定評価
初期張力を10g(標準)として20g、30gと変
化し、糸速10m/分で走行し、金属より摩擦体に
接触する前に走行糸を0.6秒間水に浸漬しあと摩
擦体に接触させた。そして金属摩擦体は種々の材
質で検討した。
摩擦体(1) 直径5cmのクロムメツキの梨地ピン
粗度 S
摩擦体(2) ステンレス棒
なお金属摩擦体は糸の走行方向の前後に毎分50
〜300回に変速・摺動できるようにしてある。糸
は30分から数時間走行させ、あと金属表面に出現
する摩耗痕を級判定して評価した。
5級(良)→1級(不良)でランク付けした。
単糸間の交絡度の測定
長さ100cmの糸条の下端にデニールの1/10の荷
重(単位(g))をかけ、上端から1cmのところ
で総単糸を2分割し、そこに細い針をさしこみそ
の針の両端にそれぞれマルチフイラメントの平均
単糸デニールに相当する(単位g)を吊し該荷重
を2cm/秒の速度で落下させ、その落下が止る回
数を読み取る。同じ操作を20回繰返して平均して
交絡度を測定した。
ウオータージエツトルームによる製織性の評価
ポリエチレンテレフタレートの糸条(50デニー
ル/24フイラメント)を経糸として整経し、通常
の紡糸油剤を用いかつインターレース処理を施す
ことなく製造したいわゆる通常の75デニール/36
フイラメントを緯糸として平組織タフタ織、経糸
総本数5000本、経密度100本/in、緯密度80/
in、織機回転数400r.p.m、ウオータージエツト、
織機(ニツサン)を用いて製織性について比較検
討し、製織20日間の稼働率の平均値をもつて比較
検討した。なお標準としてはこれまでによく行な
われている糊付したものを用い同規格で製織した
ものと比較した。
実施例1〜4、比較例1′〜4′
第1表に示す各油剤を40〜50℃に昇温均一化
し、40〜50℃の温水中に撹拌しながら注加し、濃
度10%の夫々のエマルジヨンを作成し、ローラー
式の給油法によつて1000m/分の速さで巻きとら
れつゝあるポリエチレンテレフタレート未延伸糸
(149デニール/24フイラメント)に油剤として有
効成分としての付着率が1.0%になるように夫々
付着させた。
該未延伸糸をドローツイスターを使用し、予熱
ピン温度90℃、熱セツト180℃で3.1倍に延伸しな
がらあと特公昭36−12230号公報第3図記載のも
のと同じようなインターレース機を用い圧縮空気
を噴射し単糸間同志をランダムに1m当り35ケに
交絡させた後巻取り、延伸糸を得た。各延伸糸に
ついては湿時の耐金属摩耗性及びウオータージエ
ツトルームによる製織性を評価した。
The present invention relates to a method for producing synthetic multifilament yarns. An object of the present invention is to provide a fiber yarn suitable for weaving in a water jet loom without glue using synthetic fiber multifilament as warp. Conventionally, when weaving synthetic fiber multifilament in a water jet loom, in order to impart a high degree of cohesiveness and appropriate smoothness to the threads used for the warp, preparation was traditionally carried out prior to the weaving process. In the process, a so-called sizing agent was applied, followed by after-waxing, etc., to give a high degree of cohesiveness and appropriate smoothness. This method is still used today because it provides weaving stability, but in parallel to this, it has recently become possible to weave directly using a water jet loom, omitting the sizing, drying, and waxing steps. As an attempt to achieve this, a number of methods have been proposed in which a sizing agent, such as that used in the sizing process, is blended into the spinning oil in order to impart a high degree of cohesiveness and appropriate smoothness. However, in these methods, scum-like substances are deposited in the parts corresponding to the thread guidance of various rollers and guides in the spinning process, which causes fuzz or thread breakage, especially when the fine denier for textiles, such as 50
It is known that weaving properties of filaments such as denier/24 filament are extremely low. For this reason, further study was carried out, and from the analysis of the characteristics necessary for the warp threads woven by the water jet loom, the friction strength between the threads was increased in order to suppress the generation of fuzz due to friction between the threads as much as possible. In addition, by improving the cohesiveness and suppressing the looseness of the single yarns (single fibers) that make up the fiber threads, we also reduce the friction between the metal and the yarn when wet and improve the lubricity when wet. Attempts to reduce yarn breakage and improve weaving efficiency have been proposed in JP-A-50-101694 and JP-A-51-47198. Moreover, in order to obtain a high degree of convergence, the
As has been known for a long time from No. 1175, it is also well known that a so-called interlacing process, in which single yarns constituting a multifilament are entangled with each other by fluid injection process, is performed in the silk reeling process after spinning. In this way, the main focus of the technology of improving the weavability of sizeless yarn using a water jet loom is to prevent damage to the yarn from the spinning process to the weaving process as much as possible and increase weaving efficiency by using an oil component and yarn cohesiveness. technologies are combined. It goes without saying that, as has been known up until now, a high degree of convergence and appropriate smoothness are necessary to improve the weaving efficiency of water jet looms, but weaving by water jet looms Metal abrasion resistance, especially when wet, is very important in order to improve the properties. Therefore, the present inventors did not aim to prevent single filament fuzz when wet, but rather actively protect the surfaces of reeds and heddles, and applied a protective coating to the metal surfaces of reeds and heddles. Based on the idea of forming oil, we have repeatedly considered strengthening the strength of the oil film, especially in wet conditions. As a result, from the perspective of protecting the surface of fiber yarns, compositions containing large amounts of relatively low molecular weight esters, which have low dynamic friction between the yarn and metal, have generally been effective for a long time. , waxes and silicones have similar effects. However, in actual use, if a large amount of wax is used, not only will scum build up on the drawing rollers or guides, greatly contaminating the thread guide, but also cause water to form on top of it. Even during weaving using etloom, scum often sticks to the reeds, heddles, etc., greatly reducing the weaving efficiency. Furthermore, if a large amount of water-insoluble silicones are added, the dyeability of the resulting yarn will be severely inhibited, and the silicones will re-deposit on the fabric during the dyeing process, which often causes practical problems. In addition, when the main ingredient is something with a relatively low molecular weight, such as an ester of a monobasic acid, it reduces the friction between the fiber and the metal and improves fuzz and yarn tangles caused by single yarn breakage in wet conditions. Although this is a favorable direction, it was found that there is still a limit to the preventive effect with this alone. That is, metal surfaces need to be strongly and actively protected from wear. Furthermore, in general, low molecular weight esters have poor heat resistance and are often difficult to use these days. On the other hand, with the method of increasing the molecular weight of the ester compound in order to improve heat resistance and reduce wear between the fiber and metal, the decrease in friction between the fiber and metal was smaller than expected, and what was more, On the contrary, the wear resistance of metals is on the decline. On the other hand, in recent years, in order to improve production efficiency in fiber manufacturing, higher speed and higher temperature spinning conditions have been adopted.However, from the perspective of process rationalization, synthetic fiber threads are being water jetted without glue. It has been used for weaving using thread weaving, which produces very little scum during the spinning process, and also reduces the abrasion between the metal and the thread when wet, thereby preventing single thread fuzz. A yarn with excellent metal abrasion resistance (prevention of reed abrasion) is desired, which forms a protective film more actively on the metal surface when wet, and a spinning oil agent suitable for this purpose is desired. ing. In view of the current situation, the inventors of the present invention have conducted intensive studies to obtain a synthetic fiber yarn that causes fewer troubles during the spinning and drawing processes and has excellent metal abrasion resistance even during weaving using a water jet loom. The present invention has been achieved in which the desired objective is achieved by applying a special spinning oil formulation in the process and applying interlace appropriately. That is, the present invention provides a method in which water-insoluble, limited mineral oil, ester leveling agents, waxes, and silicones are used as opposed to conventional spinning oils consisting of known leveling agents, emulsifiers, sizing agents, etc. These are completely different methods. In particular, when applying a spinning oil containing a smoothing agent and/or polyalkylene glycol to a yarn made of synthetic fibers at the stage of undrawn yarn, The copolymerization ratio of propylene oxide and ethylene oxide is 75/25 to 95/5 (weight ratio) and the molecular weight is 2000 to 2000.
15,000 water-insoluble random copolymer is blended in an amount exceeding 50% (by weight), and further contains an alkali metal salt of an alkyl phosphate having 12 to 18 carbon atoms (component A), an alkyl sulfonate having 12 to 18 carbon atoms, and /or Alkaline salt of alkyl sulfate compound (component B), modified silicones (component C), and waxes (component D) are A+ as essential components.
A if the sum of B+C+D is 4% or more and 10% or less (weight)
+B>C+D and C+D is at least 4% (by weight)
The method for producing a synthetic fiber multifilament is characterized in that the surface is treated with a spinning oil containing the composition formulated below, and an interlace treatment is performed so that 30 or more filaments per meter are randomly interlaced. The multifilament yarn has excellent glue-free weaving properties in the water jet loom as a warp, and in particular can actively reduce metal abrasion in wet conditions, greatly improving weaving efficiency. In particular, in the present invention, in order to stabilize the weaving properties without glue using the water jet loom and improve the operating rate, it is essential to combine the four components A, B, C, and D.
A surprising synergistic effect has been discovered in which the desired effect cannot be obtained even if any of these is lacking.
This fact is completely unknown until now because it is further promoted in a system with a spinning oil containing more than 50% of a water-insoluble random copolymer with a molecular weight of 2,000 to 15,000 at a ratio of 95/5 (weight ratio). . In other words, it has a completely different mechanism than the previously known ester-based smoothing agents, water-insoluble waxes, and silicones that improve metal abrasion resistance when wet, and protects the thread surface. More specifically, the present invention is intended to actively form a strong anti-wear film on the metal surface. Another important point is that the present invention improves the wear resistance of metal in wet conditions while keeping the blending ratio of each component within the lowest range due to the synergy effect.
Naturally, scum adhesion is extremely rare even in the weaving process, not to mention the silk spinning process, even when weaving without glue and using a water jet loom. Another major feature is that any of the commonly known spinning oils made of smoothing agents, emulsifiers, or polyalkylene glycols can be applied, and the copolymerization ratio of propylene oxide and ethylene oxide limited in the present invention can be applied.
Molecular weight 2000-15000 at 75/25-95/5 (weight ratio)
A water-insoluble random copolymer of
By using A, B, C and D together in more than 50% of the oil, the effects of the present invention can be brought out to the greatest extent. Furthermore, the present inventors applied a specific spinning oil and studied to further improve the weavability using a water jet loom. By manufacturing a synthetic fiber multifilament by performing an interlacing process in which single yarns are randomly interlaced using a fluid jet process as known from Publication No. 37-1175, it is possible to It was found that the effect of preventing metal abrasion in the weaving process was significantly improved, the operating rate during weaving was also improved, and excellent weavability was provided. The limited polyethers used in the present invention are water-insoluble random copolymers with a copolymerization ratio of propylene oxide and ethylene oxide of 75/25 to 95/5 (weight ratio) and a molecular weight of 2,000 to 15,000. , preferably a random copolymer of 80/20 to 90/10. These polyethers are compounds with monovalent, divalent or even polyvalent active hydrogen (e.g. -OH, -COOH, -NH 2 , -SH
It is obtained by adding ethylene oxide and propylene oxide in a random manner to a compound having the following properties using a commonly known method, and hydrophobic ones (water-insoluble) are preferred in the present invention. For example, 50/50 to 20/80 polyethers, which are known as water-soluble polyethers and have a large number of added moles of ethylene oxide, the excellent effects of the present invention are greatly reduced. Also, if the molecular weight is less than 2,000, it is difficult to maintain excellent metal wear resistance, and if it exceeds 15,000, the metal wear resistance itself is good, but the viscosity increases and the friction of the fiber against the metal during drying increases. Otherwise, sticky substances may adhere to the interlacing nozzle, resulting in poor yarn spinning stability. Next, the A, B, C and D components will be explained in detail. Component A is an alkali metal salt of a commonly known alkyl phosphate having a linear or side chain saturated or unsaturated alkyl group having 12 to 18 carbon atoms;
For example, it consists of sodium, potassium, lithium, etc. Polyoxyethylene-modified alkyl phosphates, which are usually used as anti-static agents for multifilaments, have a small number of moles, such as 1-mole adducts or 2-mole adducts, which are not effective in terms of metal wear resistance in wet conditions. completely excluded from the invention. For example, if 1 mole of ethylene oxide is added
POE(1) lauryl phosphate type is also 50%
There is a strict restriction that those containing the above are excluded from the present invention. Among the metal salts of alkyl phosphates used in the present invention, unbranched straight-chain alkyl groups are preferred, and lauryl, cetyl, palmityl, myristyl, stearyl, oleyl and the like are preferred. On the other hand, component B used in combination with component A is preferably a commonly known alkyl sulfonate having 12 to 18 carbon atoms, but may also be a sulfonate compound having a benzene nucleus in the molecule. In addition, as component B, an alkyl sulfate compound or a known ethylene oxide-modified alkyl sulfate compound in which about 1 to 3 moles of ethylene oxide is added to the alkyl group is used, and its salts include lithium, sodium, or potassium salts. Among these, sodium salts are preferably used. Furthermore, C used in combination with A component and B component
The ingredients used are modified silicones. Examples include phenyl-modified silicones, epoxy-modified silicones, polyoxyalkylene-modified silicones, fatty acid-modified silicones, etc. These modified silicones are usually commercially available emulsified with nonionic activators. be. Furthermore, A, B, C
Various known water-insoluble waxes can be used as component D to be used in combination, such as paraffin wax, oxidized microcrystalline wax,
Examples include natural and synthetic waxes such as carnauba wax, beeswax, and oxidized polyethylene wax, and paraffin waxes with a melting point of 30° C. or higher and 140° C. or lower are particularly preferred. These waxes are also generally available as dispersed in water using an emulsifier based on a nonionic active agent, and are therefore applied as an aqueous emulsion. In order to obtain the desired effect of the present invention by combining these components, A, B, C and D must be used.
Each component is always essential, and even if one component is missing, the effect cannot be fully expressed, and even if the ratio of each component is unbalanced, the metal wear resistance effect in wet conditions can be significantly improved with the minimum amount added. I can't force myself to do anything. Of course, A+B+ is beyond the scope of the present invention.
Even if the sum of C+D exceeds 10%, the effect of resisting metal wear in wet conditions is sufficiently maintained, but when the amount added increases, rolls, guides, and even reeds may be damaged during the spinning process and the weaving process in the water jet room. This is undesirable because it increases problems such as scum adhesion to the healds and healds. What is more important is that alkyl phosphates generally have anion exchange properties, and especially when weaving in a water jet loom, when the water hardness increases, water-insoluble scum obtained by ion exchange properties can be used for reeds and healds. It is also said that it is a direct cause of a decrease in operating efficiency.
Therefore, even if the blended composition used in the present invention has the effect of preventing wear of reeds and healds in wet conditions, it goes without saying that blending in more than the necessary amount should be avoided, and it is preferable to keep the amount to a minimum. do not have. Therefore, in the present invention, the sum of A+B+C+D is usually kept at 4% or more and 10% or less (by weight).
However, when A+B>C+D, the anion component is always greater than the sum of waxes and silicones, and C+D is preferably used at 4% or less. C or D
is normally a water-insoluble component, but it can be dispersed in commonly known spinning oils by dispersing it using an appropriate emulsifier.
Although 4.0% or more can of course be mixed, it is preferable to use 3.0% or less from the viewpoint of scum accumulation during the spinning and weaving processes. In this way, it is possible to exhibit excellent metal abrasion prevention effects in wet conditions without causing scum trouble during yarn spinning and weaving processes. Such a composition for preventing metal abrasion in wet conditions is usually used by being mixed with a known spinning oil, and the known spinning oil is not limited in any way. For example, known spinning oils such as smoothing agents and/or known spinning oils made of polyalkylene glycol copolymer, more specifically mineral oil, octyl-
palmitate, isotridecyl laurate, oleyl oleate, isotridecyl palmitate,
A spinning oil containing an ester compound of a monobasic acid such as isotridecyl stearate as a main component and emulsionized with a commonly known emulsifier and/or Japanese Patent Publication No. 13564/1983, British Patent No. 833450, or US Patent No. 3338830 Polyalkylene glycols, which are well known as oils for false twisting as disclosed in the specification, are spinning oils mainly composed of commonly known polyethers obtained by copolymerizing ethylene oxide and propylene oxide. However, by incorporating the composition of the present invention, it is possible to exhibit excellent wet metal wear resistance. The synthetic fibers to which the present invention is applied are synthetic fiber multifilaments made of thermoplastic synthetic fibers such as polyester and polyamide, which are obtained by melt-spinning by conventional methods, and are particularly suitable for polyethylene terephthalate-based polyester fibers. . The method for applying the spinning oil of the present invention to such synthetic fiber multifilament can be applied to the melt-spun undrawn yarn by commonly known roller oiling, spray oiling, etc., and the amount of oil applied is 0.5~ 2.0% (by weight) preferably 0.8-1.5%
(weight). As described above, the present invention provides warp threads that do not impede spinning drawability in the spinning process of synthetic fiber multifilament and also provide particularly excellent weavability even in weaving using a water jet loom without glue. This is what we provide. Next, examples of the present invention will be shown, but the present invention is not limited thereto. Further, "part" in the examples indicates weight %, and the metal abrasion resistance in wet conditions, the degree of entanglement due to interlacing, and the weavability in the examples were measured and evaluated by the following method. Measurement and evaluation of metal abrasion resistance in wet conditions The initial tension was 10g (standard), the tension was changed to 20g and 30g, the yarn was run at a speed of 10m/min, and the running yarn was soaked in water for 0.6 seconds before it came into contact with the friction body than the metal. After soaking, it was brought into contact with a friction body. We also investigated various materials for the metal friction body. Friction body (1) 5cm diameter chrome plated satin pin
Roughness S Frictional body (2) Stainless steel rod Note that the metal frictional body rotates at 50% per minute in the direction of thread travel.
It is designed to be able to shift and slide up to 300 times. The thread was run for 30 minutes to several hours, and then the wear marks that appeared on the metal surface were graded and evaluated. Ranked from grade 5 (good) to grade 1 (bad). Measurement of the degree of entanglement between single yarns Apply a load (unit: g) of 1/10 of the denier to the lower end of a 100 cm long yarn, divide the total single yarn into two at 1 cm from the upper end, and insert a thin needle into it. A load corresponding to the average single yarn denier of the multifilament (unit: g) is hung from each end of the needle, the load is dropped at a speed of 2 cm/sec, and the number of times the drop stops is read. The same operation was repeated 20 times and the average degree of confounding was measured. Evaluation of weavability using water jet loom A so-called normal 75 denier/36 yarn produced by warping polyethylene terephthalate yarn (50 denier/24 filaments) as a warp, using a normal spinning oil, and without interlacing.
Plain taffeta weave with filaments as wefts, total number of warps 5000, warp density 100/in, weft density 80/in.
in, loom rotation speed 400r.pm, water jet,
Weaving performance was compared using a loom (Nitsun), and the average operating rate for 20 days of weaving was used. As a standard, we used a pasted material, which has been commonly used up until now, and compared it with a material woven according to the same standard. Examples 1 to 4, Comparative Examples 1' to 4' Each oil agent shown in Table 1 was heated to a uniform temperature of 40 to 50°C, poured into warm water at 40 to 50°C with stirring, and diluted with a concentration of 10%. Each emulsion was created and wound at a speed of 1000 m/min using a roller-type oiling method. Each was deposited at a concentration of 1.0%. The undrawn yarn was stretched to 3.1 times using a draw twister at a preheating pin temperature of 90°C and a heat setting of 180°C, and then using an interlacing machine similar to the one described in Figure 3 of Japanese Patent Publication No. 12230/1983. Compressed air was injected to randomly entangle the single yarns with each other at a rate of 35 yarns per meter, and the yarn was then wound to obtain a drawn yarn. Each drawn yarn was evaluated for metal abrasion resistance in wet conditions and weavability in a water jet loom.
【表】
表−1に示すように本発明に用いられる疎水性
のポリエーテルと各A成分、B成分、C成分そし
てD成分の組成物は優れた耐金属摩耗性及び製織
性を示すのがわかる。それに比較して親水性のポ
リエーテル類例えば比較例1、比較例2ではその
性能が本発明に比較してやゝ低い。
実施例5〜7、比較例5′〜8′
実施例1と同じような方法で表−2の油剤組成
を付し、実施例1と同じような方法で評価を行な
つた。その結果を表−2に示した。なお用いた油
剤コンポーネントは夫々下記のものを使用した。
表−2の中のポリエーテル及びその他の成分に
ついては
*1 プロピレンオキシド/エチレンオキシドラ
ンダム共重合体90/10(末端ブタノール)
MW=4000
*2 プロピレンオキシド/エチレンオキシドラ
ンダム共重合体20/80(末端ブタノール)
MW=4000
*3 Kはカリウム塩、
*4 Naはナトリウム塩を示す。
*5 市販のパラフインワツクス(融点127〓)
エマルジヨンを使用
*6 有機酸変性シリコンエマルジヨンを使用[Table] As shown in Table 1, the composition of the hydrophobic polyether and each component A, B, C, and D used in the present invention exhibits excellent metal abrasion resistance and weavability. Recognize. In comparison, the performance of hydrophilic polyethers such as Comparative Examples 1 and 2 is much lower than that of the present invention. Examples 5 to 7, Comparative Examples 5' to 8' The oil compositions shown in Table 2 were applied in the same manner as in Example 1, and evaluation was performed in the same manner as in Example 1. The results are shown in Table-2. The oil components used were as follows. Regarding polyether and other components in Table-2 *1 Propylene oxide/ethylene oxide random copolymer 90/10 (terminal butanol)
MW=4000 *2 Propylene oxide/ethylene oxide random copolymer 20/80 (terminal butanol)
MW=4000 *3 K represents potassium salt, *4 Na represents sodium salt. *5 Commercially available paraffin wax (melting point 127〓)
Uses emulsion *6 Uses organic acid-modified silicone emulsion
【表】
表−2の結果をみてもわかるように本発明で限
定されたポリエーテル類へのA、B、C及びDの
併用は、一般公知のポリエーテルに比して優れた
摩耗性を示し、安定した製織性が得られるのがわ
かる。[Table] As can be seen from the results in Table 2, the combined use of A, B, C, and D in the polyethers specified in the present invention has superior abrasion properties compared to generally known polyethers. It can be seen that stable weavability can be obtained.
Claims (1)
滑剤及び/又はポリアルキレングリコール共重合
体を含む紡糸油剤を付与するにさいして、紡糸油
剤の有効成分に対しプロピレンオキシドとエチレ
ンオキシドの共重合比が75/25〜95/5(重量
比)で分子量2000〜15000の水不溶性ランダム共
重合体が50%(重量)を越えて配合され、更に炭
素数12〜18のアルキルホスフエート類のアルカリ
金属塩(A成分)、炭素数12〜18のアルキルスル
ホネート及び/又はアルキルサルフエート化合物
のアルカリ金属塩(B成分)、変性シリコン類
(C成分)及びワツクス類(D成分)の4者が必
須成分としてA+B+C+Dの和が4%以上10%
以下(重量)でA+B>C+D、C+Dが少なく
とも4%(重量)以下で配合された組成物を含有
する紡糸油剤で表面処理し、かつ、1m当り30ケ
以上のランダムに交絡するようにインターレース
処理を施すことを特徴とする合成繊維マルチフイ
ラメントの製造法。1. When applying a spinning oil containing a smoothing agent and/or a polyalkylene glycol copolymer to a yarn made of synthetic fibers at the undrawn yarn stage, copolymerization of propylene oxide and ethylene oxide to the active ingredients of the spinning oil. More than 50% (by weight) of a water-insoluble random copolymer with a molecular weight of 2,000 to 15,000 with a ratio of 75/25 to 95/5 (weight ratio) is blended, and an alkali of alkyl phosphates having 12 to 18 carbon atoms is added. Four components are essential: a metal salt (component A), an alkali metal salt of an alkyl sulfonate and/or alkyl sulfate compound having 12 to 18 carbon atoms (component B), modified silicones (component C), and waxes (component D). The sum of A+B+C+D as a component is 4% or more and 10%
The surface is treated with a spinning oil containing a composition containing at least 4% (by weight) of A+B>C+D, C+D as follows (by weight), and interlaced so that 30 or more entanglements per meter are randomly interlaced. A method for producing a synthetic fiber multifilament characterized by subjecting it to.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6090682A JPS58180674A (en) | 1982-04-14 | 1982-04-14 | Production of synthetic fiber multifilament yarn |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6090682A JPS58180674A (en) | 1982-04-14 | 1982-04-14 | Production of synthetic fiber multifilament yarn |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS58180674A JPS58180674A (en) | 1983-10-22 |
| JPS6247989B2 true JPS6247989B2 (en) | 1987-10-12 |
Family
ID=13155867
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP6090682A Granted JPS58180674A (en) | 1982-04-14 | 1982-04-14 | Production of synthetic fiber multifilament yarn |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS58180674A (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS61258075A (en) * | 1985-05-09 | 1986-11-15 | 東レ株式会社 | Production of relaxation heat-treated yarn |
| US9963804B2 (en) | 2014-09-30 | 2018-05-08 | Toray Industries, Inc. | Polyamide monofilament and fiber package thereof |
-
1982
- 1982-04-14 JP JP6090682A patent/JPS58180674A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS58180674A (en) | 1983-10-22 |
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