JPH02229272A - Production of polyester yarn for non-sized weaving - Google Patents
Production of polyester yarn for non-sized weavingInfo
- Publication number
- JPH02229272A JPH02229272A JP5045989A JP5045989A JPH02229272A JP H02229272 A JPH02229272 A JP H02229272A JP 5045989 A JP5045989 A JP 5045989A JP 5045989 A JP5045989 A JP 5045989A JP H02229272 A JPH02229272 A JP H02229272A
- Authority
- JP
- Japan
- Prior art keywords
- yarn
- weight
- oil
- alkyl
- weaving
- 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
- 238000009941 weaving Methods 0.000 title claims abstract description 20
- 229920000728 polyester Polymers 0.000 title claims abstract description 15
- 238000004519 manufacturing process Methods 0.000 title claims description 6
- 125000003342 alkenyl group Chemical group 0.000 claims abstract description 9
- 239000004721 Polyphenylene oxide Substances 0.000 claims abstract description 8
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 8
- 150000001875 compounds Chemical class 0.000 claims abstract description 8
- 229920000570 polyether Polymers 0.000 claims abstract description 8
- 239000002216 antistatic agent Substances 0.000 claims abstract description 6
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims abstract description 5
- 239000002736 nonionic surfactant Substances 0.000 claims abstract description 5
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims abstract description 4
- 239000000203 mixture Substances 0.000 claims abstract description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 8
- 239000003795 chemical substances by application Substances 0.000 claims description 8
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 7
- 239000000194 fatty acid Substances 0.000 claims description 7
- 229930195729 fatty acid Natural products 0.000 claims description 7
- 150000002148 esters Chemical class 0.000 claims 1
- 150000004665 fatty acids Chemical class 0.000 claims 1
- 238000004513 sizing Methods 0.000 abstract description 7
- 238000006116 polymerization reaction Methods 0.000 abstract description 2
- RPACBEVZENYWOL-XFULWGLBSA-M sodium;(2r)-2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate Chemical compound [Na+].C=1C=C(Cl)C=CC=1OCCCCCC[C@]1(C(=O)[O-])CO1 RPACBEVZENYWOL-XFULWGLBSA-M 0.000 abstract description 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 abstract description 2
- 238000002074 melt spinning Methods 0.000 abstract 2
- 150000002194 fatty esters Chemical class 0.000 abstract 1
- 239000003921 oil Substances 0.000 description 24
- 238000000034 method Methods 0.000 description 11
- -1 polyethylene terephthalate Polymers 0.000 description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 8
- 230000007423 decrease Effects 0.000 description 8
- 230000000694 effects Effects 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 6
- 239000002184 metal Substances 0.000 description 6
- 235000014676 Phragmites communis Nutrition 0.000 description 5
- 238000009987 spinning Methods 0.000 description 5
- 229920001577 copolymer Polymers 0.000 description 4
- 239000000839 emulsion Substances 0.000 description 4
- 229920000139 polyethylene terephthalate Polymers 0.000 description 4
- 239000005020 polyethylene terephthalate Substances 0.000 description 4
- 244000273256 Phragmites communis Species 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 238000007796 conventional method Methods 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 238000009940 knitting Methods 0.000 description 3
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- 238000005299 abrasion Methods 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000009499 grossing Methods 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
- 229920005604 random copolymer Polymers 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000004753 textile Substances 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 229920001634 Copolyester Polymers 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 229920002565 Polyethylene Glycol 400 Polymers 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 241001655798 Taku Species 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- BXKDSDJJOVIHMX-UHFFFAOYSA-N edrophonium chloride Chemical compound [Cl-].CC[N+](C)(C)C1=CC=CC(O)=C1 BXKDSDJJOVIHMX-UHFFFAOYSA-N 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 229940049964 oleate Drugs 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
Landscapes
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Yarns And Mechanical Finishing Of Yarns Or Ropes (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
本発明は.糊付することなく8高速ウォータージL7ト
ルーム(WJL)で製織可能な経糸用ポリエステル糸の
製造法に関するものである。[Detailed Description of the Invention] (Industrial Application Field) The present invention... The present invention relates to a method for producing polyester yarn for warp yarns that can be woven using an 8-speed water jet L7 troom (WJL) without sizing.
(従来の技術)
ポリエチレンテフタレートで代表されるポリエステルか
らなるマルチフィラメント糸は織物として広《使用され
ている。そして,近年,省力,省エネルギーを目的とし
て製織前の糊付(サイジング)を省略してWJLにより
製織する方法が広く実施されるようになってきた。(Prior Art) Multifilament yarns made of polyester, typified by polyethylene terephthalate, are widely used as textiles. In recent years, for the purpose of saving labor and energy, a method of weaving by WJL, omitting sizing before weaving, has become widely practiced.
このような無糊製織に供される糸は,糊付工程がないの
で,原糸段階で集束性が与えられていなければならない
。無糊製織可能な集束性の良い糸条を得る方法として,
集束性の良い紡糸油剤を付与したり,交絡処理を施した
りすることが行われている(特公昭53 − 4695
7号,同63 − 9080号.特開昭63 − 21
980号等)。Yarn used for such sizeless weaving does not require a sizing process, so it must be given cohesiveness at the raw yarn stage. As a method to obtain yarn with good cohesiveness that can be woven without glue,
Adding a spinning oil with good convergence and performing an entangling treatment are practiced (Japanese Patent Publication No. 53-4695).
No. 7, No. 63-9080. Japanese Patent Publication No. 1983-21
980 etc.).
しかしながら,従来の方法では,通常のWJLの製織速
度(およそ500rpm程度)においては良好な製織性
を示すが,これ以上の高速となると毛羽や糸切れが多発
し,製織性が悪《なるという問題があった。However, the conventional method shows good weaving performance at the normal WJL weaving speed (approximately 500 rpm), but when the speed is higher than this, fuzz and thread breakage occur frequently, resulting in poor weaving performance. was there.
(発明が解決しようとする課題)
本発明は,無糊状態で高速WJLで製織しても毛羽や糸
切れを発生しないポリエステル糸を製造する方法を提供
しようとするものである。(Problems to be Solved by the Invention) The present invention aims to provide a method for producing polyester yarn that does not generate fuzz or yarn breakage even when weaving at high speed WJL in a non-sizing state.
(課題を解決するための手段)
本発明は,上記課題を解決するものであり,その要旨は
次のとおりである。(Means for Solving the Problems) The present invention solves the above problems, and the gist thereof is as follows.
ポリエステルマルチフィラメント糸を製造するに際し,
溶融紡出糸条に下記の組成を有する油剤を0.5〜1.
3重量%付着させ,延伸1交絡処理を施すことを特徴と
する無糊製織用ポリエステル糸の製造法。When manufacturing polyester multifilament yarn,
An oil agent having the following composition is added to the melt-spun yarn by 0.5 to 1.
A method for producing a polyester yarn for glueless weaving, characterized by adhering 3% by weight and subjecting it to one stretching and one entangling treatment.
(alプロピレンオキシドとエチレンオキシドとが重量
比60 : 40〜20 ; 80でランダムに共重合
され.平均分子量が4000〜iooooのポリエーテ
ル化合物20〜50重量%
(bl次式で表される脂肪酸エステル20〜40重量%
R’COOR’
(Rl は炭素原子数7〜20のアルキル基又はアルケ
ニル基 Btは炭素原子数5〜18のアルキル基又はア
ルケニル基。)
(c)式(イ)〜(ニ)で表される非イオン界面活性剤
10〜30重景%
O R 3C O O ( C H z C H 2
0 ) n H@ R’COO(CHzCHzO)n
OcR’Cl R110(CHzCHzO)nHO
R’O(CH!CH.O)nR’
(Rff〜R8は炭素原子数8〜1日のアルキル基又は
アルケニル基,nは4〜20の整数。)+d) 制電
剤 3〜13重量%以下,本発明
につい”C詳細に説明する。(propylene oxide and ethylene oxide are randomly copolymerized at a weight ratio of 60: 40 to 20; ~40% by weight
R'COOR' (Rl is an alkyl group or alkenyl group having 7 to 20 carbon atoms; Bt is an alkyl group or alkenyl group having 5 to 18 carbon atoms.) (c) Represented by formulas (a) to (d) Nonionic surfactant 10-30% O R 3C O O (C Hz C H 2
0 ) n H@R'COO(CHzCHzO)n
OcR'Cl R110(CHzCHzO)nHO
R'O(CH!CH.O)nR' (Rff to R8 are alkyl or alkenyl groups having 8 to 1 carbon atoms, n is an integer of 4 to 20.) + d) Antistatic agent 3 to 13% by weight The present invention will be explained in detail below.
まず,本発明は,溶融紡出糸条に,特定のプロピレンオ
キシドとエチレンオキシドとのランダム共重合体(PO
/EO共重合体という)系ポリエーテル化合物.脂肪酸
エステル,非イオン界面活性剤及び制電剤を特定の割合
で配合した紡糸油剤を付与することを特徴とするもので
ある。First, the present invention uses a specific random copolymer of propylene oxide and ethylene oxide (PO
/EO copolymer) type polyether compound. It is characterized by applying a spinning oil containing a fatty acid ester, a nonionic surfactant, and an antistatic agent in a specific ratio.
一般に織物に供されるポリエステル糸用の紡糸油剤とし
ては,平滑性.集束性.制電性等を向上させるため鉱物
油や各種の脂肪酸エステル等を組み合わせたものが多く
使用されており,WJLで無糊で製織するためのポリエ
ステル糸用としてはポリエーテル化合物も用いられてい
る。Generally, the spinning oil for polyester yarn used in textiles has a smoothness. Convergence. Combinations of mineral oil and various fatty acid esters are often used to improve antistatic properties, and polyether compounds are also used for polyester yarns for glueless weaving in WJL.
本発明者らは,高速WJLによる無糊製織を円滑に行う
ためには,平滑性,集束性,制電性のほかに,次のよう
な要件が必要であることに注目して鋭意検討した。The inventors of the present invention have conducted intensive studies, noting that in addition to smoothness, convergence, and antistatic properties, the following requirements are necessary in order to smoothly perform glueless weaving using high-speed WJL. .
■ 緯糸を水噴射によって打ち込むとき,経糸の油剤が
脱落しにクク,筬の擦過による強度低下を防ぐこと。■ When driving the weft yarns by water jet, prevent the oil from falling off from the warp yarns and reduce strength due to scratches on the reed.
■ 経糸が綜絖によって,屈曲や擦過を受けたときの糸
の強度低下を小さくすること。■ Minimize the decrease in strength of the warp threads when they are bent or abraded by the heddles.
■ 整経工程において.ガイドやテンサーで糸が擦過さ
れた時の糸の強度低下を小さくすること。■ In the warping process. To reduce the decrease in the strength of a thread when it is rubbed by a guide or tensor.
■ 製織時において,糸と糸のこすれによる強度低下を
小さくすること。■ Minimize the decrease in strength due to thread rubbing during weaving.
その結果,上記特定の油剤を付与することにより.これ
らの要件が満足され1糸切れや毛羽の発生が防止され,
製織性が向上することを見出し本発明に到達したのであ
る。As a result, by applying the specific oil agent mentioned above. These requirements are met and thread breakage and fuzz are prevented.
They discovered that the weavability was improved and arrived at the present invention.
本発明における(a+成分のPO/EO共重合体系ポリ
エーテル化合物は,糸とガイド,糸と金属,糸と糸の摩
擦による強度低下を防ぐ作用をするものであって,ブロ
ビレンオキシドとエチレンオキシドとの重量比が60
j 40〜20 : 80のランダム共重合体で,平均
分子量が4000〜10000のものであることが必要
であり,これを油剤中に20〜50重量%配合すること
が必要である。プロピレンオキシドの比率が60重景%
を超えると粘性が高くなって,平滑性が乏しくなり,強
度低下を引き起こし,逆にこの比率が20重量%より小
さくなると粘性が低くなり,クッシヲン的効果がなくな
ってしまい.同様に強度低下を引き起こす。また,ポリ
エーテル化合物の分子量が4000未満であったり,配
合量が20重量%未満であると油剤全体としての粘性が
下がり.前述したクッション的効果がなくなり,逆に分
子量がiooooを超えたり,配合量が50重量%を超
えると油剤全体としての粘性が高くなり,糸とガイド及
び金属.糸と糸のFJ擦によって強度低下を引き起こす
。さらに,水による糸条表面油剤の脱落性もポリエーテ
ルの分子量によって大きく左右され.分子量が4000
未満になると水によって油剤がほとんど脱落してしまう
。逆に分子量が高くなれば脱落しに《くなるが.前述し
たように平滑性や強度低下の面からあまり高くすること
は好ましくな< ,10000以下にするのが適当であ
る。In the present invention, the PO/EO copolymer-based polyether compound (a+ component) has the function of preventing strength reduction due to friction between thread and guide, thread and metal, and thread and thread, and has the function of preventing strength reduction due to friction between thread and guide, thread and metal, and thread and thread, and is a compound that prevents strength reduction due to friction between thread and guide, thread and metal, and thread and thread. The weight ratio of
j 40-20: It is necessary to be a random copolymer of 80 and have an average molecular weight of 4000-10000, and it is necessary to mix 20-50% by weight of this in the oil agent. Propylene oxide ratio is 60%
When this ratio exceeds 20% by weight, the viscosity becomes high, resulting in poor smoothness and a decrease in strength.On the other hand, when this ratio is less than 20% by weight, the viscosity becomes low and the cushion-like effect is lost. Similarly, it causes a decrease in strength. Furthermore, if the molecular weight of the polyether compound is less than 4,000 or the blending amount is less than 20% by weight, the viscosity of the oil agent as a whole decreases. The above-mentioned cushioning effect disappears, and conversely, if the molecular weight exceeds ioooo or the blending amount exceeds 50% by weight, the viscosity of the oil as a whole becomes high, and the thread, guide, and metal. FJ friction between threads causes a decrease in strength. Furthermore, the ability of the yarn surface oil to be removed by water is greatly influenced by the molecular weight of the polyether. Molecular weight is 4000
If it is less than that, most of the oil will fall off due to water. On the other hand, as the molecular weight increases, it becomes more likely to fall off. As mentioned above, it is preferable to set the value to less than 10,000, since it is not preferable to make the value too high in terms of smoothness and strength deterioration.
次に.(b)成分の脂肪酸エステルは平滑剤として作用
するものであって,前記の式で表される脂肪酸エステル
を20〜40重量%配合することが必要である。脂肪酸
エステルの炭素原子数が多くなると粘性が増し,平滑性
が劣ったり,水によるエマルジョン化が難しくなる。ま
た,炭素原子数が少ない(分子量が小さい)と延伸,熱
処理時に分解したり,糸に付着後,長時間経時すると分
解が生じ低分子量になった油剤が糸に膨濶等の悪影響を
与え,強度低下を引き起こすので好ましくない。また,
脂肪酸エステルの配合量が20重量%未満であると平滑
性が不十分となり.40重量%を超えるとポリエーテル
化合物の特徴が発揮できなくなるので好ましくない。next. The fatty acid ester of component (b) acts as a smoothing agent, and it is necessary to blend 20 to 40% by weight of the fatty acid ester represented by the above formula. When the number of carbon atoms in a fatty acid ester increases, its viscosity increases, resulting in poor smoothness and difficulty in forming an emulsion with water. In addition, if the number of carbon atoms is small (low molecular weight), it may decompose during drawing or heat treatment, or after being attached to the thread, it may decompose over a long period of time, resulting in low molecular weight oils that may have adverse effects on the thread, such as swelling. This is not preferable because it causes a decrease in strength. Also,
If the amount of fatty acid ester blended is less than 20% by weight, the smoothness will be insufficient. If it exceeds 40% by weight, it is not preferable because the characteristics of the polyether compound cannot be exhibited.
また,(C)成分の非イオン界面活性剤は,平滑剤を水
性エマルジョン化するための乳化剤として作用するとと
もに糸と糸との摩擦による強度低下を防ぐ効果を発揮す
るもので,前記式(イ)〜(ニ)で表されるものを10
〜30重量%配合することが必要である。In addition, the nonionic surfactant as component (C) acts as an emulsifier to turn the smoothing agent into an aqueous emulsion, and also has the effect of preventing strength reduction due to friction between threads. ) to (d) are expressed as 10
It is necessary to mix up to 30% by weight.
最後に,(d)成分の制電剤は,糸条の静電気の帯電を
防止し1糸条の取扱を容易にするものであり,スルホネ
ートNa塩やホスフェートK塩等が使用され,配合量は
(a)〜(C)の成分の作用を損なわない3〜13重量
%が適当である。Finally, component (d) is an antistatic agent that prevents static electricity from charging the yarn and makes it easier to handle each yarn. Sulfonate Na salt, phosphate K salt, etc. are used, and the amount of the antistatic agent is determined by the amount. A suitable amount is 3 to 13% by weight, which does not impair the effects of components (a) to (C).
なお,本発明における紡糸油剤には,(a)〜(d)の
成分のほかに,各成分の相溶性を高めたり,pHを調整
したりするための調整剤,例えば,エチレングリコール
,プロピレングリコール等の低級アルコール,オレイン
酸等の弱酸性物質及びオレイン酸Na等の弱塩基性物質
等を少量配合してもよい。In addition to the components (a) to (d), the spinning oil in the present invention may also contain adjusting agents for increasing the compatibility of each component and adjusting the pH, such as ethylene glycol and propylene glycol. A small amount of a lower alcohol such as, a weakly acidic substance such as oleic acid, a weakly basic substance such as Na oleate, etc. may be blended.
本発明における油剤の付与方法としては,通常水性エマ
ルジョンとしてローラ給油法又はスリット給油法が採用
される。As a method for applying the oil in the present invention, a roller oiling method or a slit oiling method is usually adopted as an aqueous emulsion.
また,油剤付与量は0.5〜1.3重量%とすることが
必要であり,この付与量があまり少ないと延伸時.整経
時及び製織時に糸切れや毛羽を多発し,逆に多すぎると
延伸後の交絡付与時に交絡がかかりにくくなったり,W
JLによる製織時に過剰の油剤が飛散し,筬等を汚染し
たりする原因となるので好ましくない。In addition, the amount of oil applied needs to be 0.5 to 1.3% by weight, and if this amount is too small, problems will occur during stretching. Yarn breakage and fuzz occur frequently during warping and weaving, and conversely, if there is too much yarn, it becomes difficult to entangle when applying entanglement after drawing, and W
This is not preferable since excessive oil is scattered during weaving by JL and may contaminate the reeds and the like.
また,交絡処理は,通常,延伸後に行われ,交絡度が3
0個/m以上になるように処理される。In addition, the entanglement process is usually performed after stretching, and the degree of entanglement is 3.
It is processed so that it becomes 0 pieces/m or more.
なお.本発明におけるポリエステルとしてはポリエチレ
ンテレフタレート及びこれを主体とする各種共重合ポリ
エステルが使用される。共重合成分の具体例としては,
イソフタル酸,5−ナトリウムスルホイソフタル酸,ア
ジピン酸,セバシン酸,ジエチレングリコール,ネオベ
ンチルグルコール等が挙げられる。In addition. As the polyester in the present invention, polyethylene terephthalate and various copolyesters mainly composed of polyethylene terephthalate are used. Specific examples of copolymer components include:
Examples include isophthalic acid, 5-sodium sulfoisophthalic acid, adipic acid, sebacic acid, diethylene glycol, neobentyl glycol, and the like.
(実施例) 次に,本発明を実施例によって具体的に説明する。(Example) Next, the present invention will be specifically explained using examples.
なお,実施例中の特性値は次の方法で測定したものであ
る。Note that the characteristic values in the examples were measured by the following method.
冫 ・ (OPU)
n−へブタンによって,糸に付着した油剤を抽出し,n
−ヘプタンを蒸発乾固させ,油剤の重量を測定して算出
した。・(OPU) Extract the oil adhering to the thread with n-hebutane, and
- Calculated by evaporating heptane to dryness and measuring the weight of the oil.
又流度
米国特許2985955号記載された方法に準じて測定
した。The flow rate was also measured according to the method described in US Pat. No. 2,985,955.
3jLlll支
オリエンティック社製テンシロンUTM−4−100型
を用い,試料長500mm,引張速度500mm /分
で測定した。The measurement was performed using Tensilon UTM-4-100 manufactured by Orientic Co., Ltd., with a sample length of 500 mm and a tensile speed of 500 mm/min.
儲1r鐸81東変
第1図の装置を用い,供給テンション20g,糸速20
0m /分で糸を擦過させた後,強伸度を測定した。Using the equipment shown in Fig. 1 of Tsuru 1r Taku 81 Tohen, the supply tension was 20 g, and the yarn speed was 20.
After rubbing the yarn at 0 m/min, the strength and elongation was measured.
対途j律ロ1張敗
渡辺測器社製μ−メーターを用い,糸速度200m/分
,摩擦体16mmφクロl、梨地ビン,接触角90度,
T+=20gで測定した。Using a μ-meter manufactured by Watanabe Sokki Co., Ltd., thread speed 200 m/min, friction body 16 mmφ black l, satin finish bottle, contact angle 90 degrees,
Measured with T+=20g.
氷拉よA皿落度
第2図に示した装置を用い,糸速200m/分で,30
゜Cの水中を通過させた後のOPUを測定した。Using the apparatus shown in Figure 2, the yarn speed is 200 m/min, 30 m/min.
The OPU was measured after passing through water at °C.
/ ラビング (F/Fラビング )
第3図に示した装置を用い,荷重ioo g ,捻り回
数3回,100ストローク/分の速度で糸と糸をこすり
,切断するまでの回数を測定した。/ Rubbing (F/F Rubbing) Using the apparatus shown in Fig. 3, the threads were rubbed at a load of ioo g, three twists, and a speed of 100 strokes/min, and the number of times until the threads were cut was measured.
筬1111度
第4図に示したモデル装置を用い,糸速100m/分,
供給テンション20gで編針を糸で60分間擦過させた
後,編針の摩耗状況を観察して,次の3段階で判定した
。Using the model device shown in Figure 4 with a reed of 1111 degrees and a yarn speed of 100 m/min,
After rubbing the knitting needles with the yarn for 60 minutes at a supply tension of 20 g, the wear status of the knitting needles was observed and evaluated in the following three stages.
○:殆ど摩耗なし,△:やや摩耗あり,×:摩耗が著し
い。○: Almost no wear, △: Slight wear, ×: Significant wear.
なお.第1〜4図において.Yは測定糸条,1は延伸糸
バーン,2は張力調整器.3は梨地ビン,4は引取りロ
ーラ,5は巻取機,6は水浴,7は荷重、8.9はフリ
ーローラ,10は糸条固定具,12は編針を示す。In addition. In Figures 1-4. Y is the measuring yarn, 1 is the drawing yarn burn, and 2 is the tension adjuster. 3 is a satin finish bin, 4 is a take-up roller, 5 is a winder, 6 is a water bath, 7 is a load, 8.9 is a free roller, 10 is a yarn fixing device, and 12 is a knitting needle.
実施例1〜4,比較例1〜3
ポリエチレンテレフタレートを常法によって溶融紡糸し
,紡出糸条に,第1表に示した組成の油剤の12%水性
エマルジ目ン液をローラ給油法により油剤付着量が0.
9〜1.1重量%になるように,ローラ凹転数を変えて
付与して.未延伸糸を得た。Examples 1 to 4, Comparative Examples 1 to 3 Polyethylene terephthalate was melt-spun by a conventional method, and a 12% aqueous emulsion liquid having the composition shown in Table 1 was applied to the spun yarn using a roller lubrication method. Adhesion amount is 0.
The concave rotation speed of the roller was changed so that the amount was 9 to 1.1% by weight. An undrawn yarn was obtained.
第1表
なお,第1表において,油剤成分の量は重量部を示し.
PO/EOO後の( )内の数値は5共重合重量比,
Mwは分子量, PEG(400)は分子量400の
ポリエチレングリコール. POE(5)は重合度5の
ポリオキシエチレン, EGはエチレングリコールを意
味する。Table 1 In Table 1, the amounts of oil components are in parts by weight.
The numbers in parentheses after PO/EOO are 5 copolymer weight ratios,
Mw is the molecular weight, and PEG (400) is polyethylene glycol with a molecular weight of 400. POE (5) means polyoxyethylene with a degree of polymerization of 5, and EG means ethylene glycol.
この未延伸糸を常法によって延伸し,延伸直後において
交絡処理を施し,交絡度40〜50個/mで50d/1
8fの延伸糸を得た。This undrawn yarn was stretched by a conventional method, and immediately after stretching, it was subjected to an intertwining treatment, and the degree of entanglement was 40 to 50 pieces/m, and 50 d/1
A drawn yarn of 8 f was obtained.
この延伸糸の特性を第2表に示す。The properties of this drawn yarn are shown in Table 2.
第2表から明らかなように本発明の実施例で得られた糸
条は平滑性(対金属摩擦係数),糸と金属のこすれによ
る強度低下の度合,糸と糸のこすれによる糸の切断度合
(F/Fラビング性),水による油剤の脱落度.筬の摩
耗度の全ての面ですぐれていることがわかる。As is clear from Table 2, the yarns obtained in the examples of the present invention have smoothness (coefficient of friction against metal), degree of strength reduction due to thread-to-metal rubbing, and degree of yarn breakage due to thread-to-thread rubbing. (F/F rubbing property), degree of shedding of oil by water. It can be seen that the reeds are excellent in all aspects of wear.
第2表
これに対し,比較例の糸条では,回転数700rpmO
製織速度になると極端に製織性が悪くなるのがわかる。Table 2: On the other hand, with the yarn of the comparative example, the rotation speed was 700 rpm.
It can be seen that the weaving performance becomes extremely poor as the weaving speed increases.
次に.この糸条を経糸として用い,加撚,糊付けを行わ
ずに同一条件で.津田駒社製WJI,:ZW−303を
用い,回転数50Orpm及び700rpn+の速度で
製織した結果を第3表に示す。next. This yarn was used as the warp yarn under the same conditions without twisting or sizing. Table 3 shows the results of weaving using WJI:ZW-303 manufactured by Tsudakoma Co., Ltd. at a rotation speed of 50 rpm and 700 rpm+.
第3表から明らかなように本発明の紡糸油剤を用いた糸
条は回転数500rPm及び700rpmの製織速度の
いずれでも製織性に優れていることがわかる。As is clear from Table 3, the yarn using the spinning oil of the present invention has excellent weavability at both the weaving speeds of 500 rPm and 700 rpm.
(発明の効果)
本発明によれば,特定油剤の付与と交絡との相乗効果に
より,無糊状態で高速WJLで製織しても毛羽や糸切れ
を発生しないポリエステル糸を製造することが可能とな
る。(Effects of the Invention) According to the present invention, due to the synergistic effect of application of a specific oil and entanglement, it is possible to produce polyester yarn that does not generate fuzz or yarn breakage even when woven at high speed WJL in a non-sizing state. Become.
第1〜4図は実施例における糸条の特性値を測定するた
めの装置の説明図であり.第1図は擦過後の強伸度を測
定するための擦過装置.第2図は油剤の水による脱落度
を測定するための油剤脱落装置.第3図はF’ / F
ラビング性を測定する装置第4図は筬の摩耗度を測定す
る装置を示す。
特許出願人 日本エステル株式会社Figures 1 to 4 are explanatory diagrams of an apparatus for measuring the characteristic values of yarn in Examples. Figure 1 shows the abrasion device used to measure strength and elongation after abrasion. Figure 2 shows an oil removal device for measuring the degree of removal of oil from water. Figure 3 shows F'/F
Apparatus for Measuring Rubbing Properties FIG. 4 shows an apparatus for measuring the degree of wear of reeds. Patent applicant Nippon Ester Co., Ltd.
Claims (1)
際し、溶融紡出糸条に下記の組成を有する油剤を0.5
〜1.3重量%付着させ、延伸、交絡処理を施すことを
特徴とする無糊製織用ポリエステル糸の製造法。 (a)プロピレンオキシドとエチレンオキシドとが重量
比60:40〜20:80でランダムに共重合され、平
均分子量が4000〜10000のポリエーテル化合物
20〜50重量% (b)次式で表される脂肪酸エステル 20〜40重量
% R^1COOR^2 (R^1は炭素原子数7〜20のアルキル基又はアルケ
ニル基、R^2は炭素原子数5〜18のアルキル基又は
アルケニル基。) (c)式(イ)〜(ニ)で表される非イオン界面活性剤
10〜30重量% (イ)R^3COO(CH_2CH_2O)_nH (ロ)R^4COO(CH_2CH_2O)_nOCR
^5 (ハ)R^6O(CH_2CH_2O)_nH (ニ)R^7O(CH_2CH_2O)_nR^6 (R^3〜R^6は炭素原子数8〜18のアルキル基又
はアルケニル基、nは4〜20の整数。) (d)制電剤 3〜13重量%(1) When producing polyester multifilament yarn, add 0.5 of an oil agent having the following composition to the melt-spun yarn.
A method for producing a polyester yarn for glueless weaving, characterized by adhering ~1.3% by weight, and subjecting it to stretching and entangling treatment. (a) A polyether compound in which propylene oxide and ethylene oxide are randomly copolymerized at a weight ratio of 60:40 to 20:80 and whose average molecular weight is 4,000 to 10,000 20 to 50% by weight (b) Fatty acid represented by the following formula Ester 20-40% by weight R^1COOR^2 (R^1 is an alkyl group or alkenyl group having 7 to 20 carbon atoms, R^2 is an alkyl group or alkenyl group having 5 to 18 carbon atoms.) (c) 10 to 30% by weight of nonionic surfactants represented by formulas (a) to (d) (a) R^3COO(CH_2CH_2O)_nH (b) R^4COO(CH_2CH_2O)_nOCR
^5 (c) R^6O(CH_2CH_2O)_nH (d) R^7O(CH_2CH_2O)_nR^6 (R^3 to R^6 are alkyl or alkenyl groups having 8 to 18 carbon atoms, n is 4 to An integer of 20.) (d) Antistatic agent 3 to 13% by weight
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5045989A JPH02229272A (en) | 1989-03-02 | 1989-03-02 | Production of polyester yarn for non-sized weaving |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5045989A JPH02229272A (en) | 1989-03-02 | 1989-03-02 | Production of polyester yarn for non-sized weaving |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH02229272A true JPH02229272A (en) | 1990-09-12 |
Family
ID=12859458
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP5045989A Pending JPH02229272A (en) | 1989-03-02 | 1989-03-02 | Production of polyester yarn for non-sized weaving |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH02229272A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1999039041A1 (en) * | 1998-01-29 | 1999-08-05 | Asahi Kasei Kogyo Kabushiki Kaisha | Smooth polyester fiber |
CN102912633A (en) * | 2012-09-29 | 2013-02-06 | 南通恒淼纺织科技有限公司 | Water-soluble polyester sizing agent and preparation thereof |
-
1989
- 1989-03-02 JP JP5045989A patent/JPH02229272A/en active Pending
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1999039041A1 (en) * | 1998-01-29 | 1999-08-05 | Asahi Kasei Kogyo Kabushiki Kaisha | Smooth polyester fiber |
US6468655B1 (en) | 1998-01-29 | 2002-10-22 | Asahi Kasei Kabushiki Kaisha | Smooth polyester fiber |
KR100378857B1 (en) * | 1998-01-29 | 2003-04-07 | 아사히 가세이 가부시키가이샤 | Smooth polyester fiber |
CN102912633A (en) * | 2012-09-29 | 2013-02-06 | 南通恒淼纺织科技有限公司 | Water-soluble polyester sizing agent and preparation thereof |
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