JPH0291273A - Lubricant suitable for high-speed frictional false-twisting - Google Patents
Lubricant suitable for high-speed frictional false-twistingInfo
- Publication number
- JPH0291273A JPH0291273A JP14388688A JP14388688A JPH0291273A JP H0291273 A JPH0291273 A JP H0291273A JP 14388688 A JP14388688 A JP 14388688A JP 14388688 A JP14388688 A JP 14388688A JP H0291273 A JPH0291273 A JP H0291273A
- Authority
- JP
- Japan
- Prior art keywords
- compound
- yarn
- molecular weight
- twisting
- false
- 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
- 239000000314 lubricant Substances 0.000 title abstract description 5
- 150000001875 compounds Chemical class 0.000 claims abstract description 36
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims abstract description 20
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims abstract description 20
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims abstract description 10
- 150000005846 sugar alcohols Polymers 0.000 claims abstract description 9
- -1 polytetramethylene Polymers 0.000 claims abstract description 7
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims abstract description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims abstract description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 24
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 239000000470 constituent Substances 0.000 claims description 3
- 229920005604 random copolymer Polymers 0.000 abstract description 6
- 229920001400 block copolymer Polymers 0.000 abstract description 5
- 238000002156 mixing Methods 0.000 abstract description 3
- 238000013329 compounding Methods 0.000 abstract description 2
- 239000003921 oil Substances 0.000 description 31
- 239000004744 fabric Substances 0.000 description 9
- 239000000835 fiber Substances 0.000 description 8
- 229920000728 polyester Polymers 0.000 description 8
- 230000000694 effects Effects 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- 239000004721 Polyphenylene oxide Substances 0.000 description 5
- 229920000570 polyether Polymers 0.000 description 5
- 230000002159 abnormal effect Effects 0.000 description 3
- 238000011109 contamination Methods 0.000 description 3
- 238000002788 crimping Methods 0.000 description 3
- 238000009987 spinning Methods 0.000 description 3
- 239000002759 woven fabric Substances 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 238000009825 accumulation Methods 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 239000010802 sludge Substances 0.000 description 2
- 230000003068 static effect Effects 0.000 description 2
- 238000005728 strengthening Methods 0.000 description 2
- 241001589086 Bellapiscis medius Species 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- 229920006311 Urethane elastomer Polymers 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 239000002075 main ingredient Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000002522 swelling effect Effects 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
Abstract
Description
【発明の詳細な説明】
〈産業上の利用分野〉
本発明は、主としてポリエステル繊維の高速延伸摩擦仮
撚に適した油剤に関するものであり、より詳しくは高速
摩擦仮撚に際してヒータ汚れが殆んど観察されず、均斉
性の優れたニット編地や熾物布地を提供し得る加工糸製
造用油剤、特に晶速延伸仮撚用油剤に関するものである
。[Detailed Description of the Invention] <Industrial Application Field> The present invention mainly relates to an oil agent suitable for high-speed drawing friction false-twisting of polyester fibers, and more specifically, it relates to an oil agent suitable for high-speed friction false-twisting of polyester fibers. The present invention relates to a lubricant for producing processed yarn, in particular a lubricant for crystal speed stretching and false twisting, which can produce knitted fabrics and knitted fabrics with excellent uniformity without being observed.
〈従来の技術〉
従来、ポリエステル繊維の加工糸を得る方法として、紡
糸後の未延伸糸ヲー吐延伸糸とし2てから仮撚する方法
と紡糸原糸から延伸と仮撚とを同時または連続的に行な
う方法があり、峻近の技術の進歩により後者の延伸同時
仮撚が主体となっているうそしてかかる延伸仮撚付与方
法として、スピンドル仮撚方法およびA1.−JX仮撚
方法が採用されており、特に摩擦仮撚方式の採用によっ
て加工速度は400〜1000m/分のように飛躍的に
向上しつつある0
〈発明が解決しようとする課題〉
しかし100工速朋の上昇に伴って、糸と各種接触体(
例えばガイド、ローラー ヒータ)との摩擦の増大によ
り繊維の損傷による毛羽の発生および断糸の発生などが
増大するという欠点が現われる。<Prior art> Conventionally, methods for obtaining processed yarns of polyester fibers include a method in which an undrawn yarn after spinning is discharged as a drawn yarn and then false-twisted, and a method in which drawing and false-twisting are performed simultaneously or continuously from a spun raw yarn. However, due to recent advances in technology, the latter, simultaneous stretching and false twisting, has become the main method. -The JX false-twisting method has been adopted, and the processing speed is increasing dramatically to 400 to 1000 m/min, especially by adopting the frictional false-twisting method. As speed increases, the thread and various contact objects (
For example, the disadvantage is that increased friction with guides, roller heaters) increases the occurrence of fuzz and yarn breakage due to damage to the fibers.
また一方で、仮撚速度の増大により従来よく知られてい
る仮撚油剤ではヒーターが著しく汚染されて、極端な場
合にはヒーター上にタール化物やスラッジ残査(以後ス
カムと称する)が堆積し、これが原因で加工糸の毛羽の
発生や断糸の発生が増大することとなる。さらにまた、
捲縮異常品の発生や染色斑の色土の原因となり、ニット
編地の線膜や織物布池に篩などが発生する。そのため生
産を停止してヒーターの掃除を頻繁に実施しなければな
らず、操業性を大きく損うこととなる。On the other hand, due to the increased false-twisting speed, conventionally well-known false-twisting oils can cause significant contamination of the heater, and in extreme cases can lead to the accumulation of tar and sludge residue (hereinafter referred to as scum) on the heater. This increases the occurrence of fuzz and yarn breakage in the processed yarn. Furthermore,
It causes abnormal crimping and uneven dyeing, and causes lines in knitted fabrics and sieves in woven fabrics. Therefore, production must be stopped and heaters must be cleaned frequently, which greatly impairs operability.
最近耐熱性の油剤が検討されており、その一つにポリエ
ーテル化合物を主体とした油剤が種々提案されている。Recently, heat-resistant oils have been studied, and various oils based on polyether compounds have been proposed.
そしてかかるポリエーテルを主成分とする油剤を付与し
友ポリエステルマルチフィラメント糸を延伸同時仮[−
行なうと、ヒーター汚fLに対しては良好な結果が得ら
nl、断糸および毛羽の防止に効果が得られている。し
かしながら、近年の延伸同時仮撚加工の加工速度の高速
化に伴ない、ヒーター温度も200℃以上の高温となり
、しかも捲縮加工糸の細デニール化の要求が高捷りつつ
ある。このような、+iF1デニール加工糸を高速摩擦
仮撚下で得る際に、前記のポリエーテルを主成分とする
油剤を使用すると、ヒーター汚れが悪化し、操業時間と
共に断糸が多くなり、また得らオした加工糸の毛羽も多
くなる。Then, an oil agent containing such polyether as a main component is applied, and the polyester multifilament yarn is stretched simultaneously [-
When carried out, good results were obtained for heater stains fL, and effects were obtained for preventing yarn breakage and fuzz. However, in recent years, as the processing speed of simultaneous drawing and false twisting has increased, the heater temperature has also increased to a high temperature of 200° C. or more, and there is a growing demand for finer denier crimped yarns. When obtaining such +iF1 denier textured yarn under high-speed friction false twisting, if the above-mentioned oil agent mainly composed of polyether is used, heater contamination will worsen, yarn breakage will increase over time, and yarn breakage will increase over time. The fluff of the processed yarn that has been twisted also increases.
このために、単1JI1.維デニールが1.2デニール
Ll。For this purpose, single JI1. The fiber denier is 1.2 denier Ll.
下である細デニール糸を加工速度soom、、’分以上
の高速摩擦仮撚で仮撚加工して生産することは極めて鼎
しく不可能に近い状態であった。It has been extremely difficult and nearly impossible to produce the fine denier yarn shown below by false twisting at high speed friction false twisting at a processing speed of 1,000 minutes or more.
〈課題を解決する之めの手段〉
本発明者は、これら問題点を解決することを目的に鋭意
研究を行なった結果、ヒーター汚れが少なく毛羽の発生
や断糸の発生が少なく、さらに捲縮性の均一な線膜の発
生がない加工糸が得られる本発明油剤に到達したもので
ある。すなわち本発明は、細デニール加工糸、特に単繊
維繊度1.2デニール以下の加工糸を加工速度400m
/分〜1000m/分のような高速摩擦仮撚を行なうに
際して、前述したような種々の弊害をもたらさないとこ
ろの高速摩擦仮撚用油剤を提供するものである。<Means for Solving the Problems> As a result of intensive research aimed at solving these problems, the inventor of the present invention has found that there is less heater dirt, less fuzzing, less occurrence of yarn breakage, and even less crimping. The oil agent of the present invention has been achieved which allows processed yarns with uniform properties and no streaks to be produced. That is, the present invention processes fine denier processed yarn, particularly processed yarn with a single fiber fineness of 1.2 denier or less, at a processing speed of 400 m.
The present invention provides an oil agent for high-speed friction false-twisting that does not cause the various disadvantages mentioned above when performing high-speed friction false-twisting at speeds of 1000 m/min to 1000 m/min.
本発明は、高速摩擦仮撚を行なうに際して前述したよう
な欠点を防止するために、下記■〜のの成分を配合した
油剤を用いるものである。In the present invention, in order to prevent the above-mentioned drawbacks when performing high-speed friction false twisting, an oil agent containing the following components (1) to (1) is used.
■多価アルコールにエチレンオキサイド(aO)とプロ
ピレンオキサイド(PO)がプロツク共重合状に!九は
ランダム共重合状に付加されており、PO/EO(モル
比)が40/60〜90/10であって、実質的に全て
の末端が炭素数1〜12のアルキル基によってエーテル
結合封鎖されており、かつ分子量が1000〜5000
である化合物を30〜70重tチ、
Oポリテトラメチレングリコールにエチレンオキサイ)
”(EO)トブロピレ/オキサイド(PO )がランダ
ム共重合状に付加されており、PO/EO(モル比)が
20/80〜80/20であって、かつ分子量が250
0〜10000である化合物を20〜60重fitチ、
ノ多価アルコールにエチレンオキサイド(EO)とプロ
ピレンオキサイド(PO)がランダム共重合状に付加さ
れており、PO/EO(モル比)が20/80〜80/
20であって、実質的に末端が封鎖されておらず、かつ
分子量が1sooo〜28000である化合物t−2〜
10重1チ、以下に本発明の構成成分■〜のについて、
そしてその役割とそnを特定した根拠について説明する
0
まず成分のは、全末端基をアルキル基により封鎖されて
おり、これにより糸の平滑性をより向上させ、高速摩擦
仮撚における毛羽や断糸を減少させ、さらに捲縮異常品
を少なくシ、ニット編地の線膜や織物布地の筋の発生の
少ない加工糸が得られる。またヒーター汚れも非常に少
なく良好である。ここでPO/EO(モル比)を40/
60〜90/10とした理由は、ヒーター汚れを少なく
する之めである。また化合物■の分子量が1000未満
の場合には、対金属摩擦など流体潤滑性の点では好まし
いが、熱安定性に乏しく、それと共にゴム膨潤性が悪化
するので好ましくない。逆に分子量が5ooot越える
と摩擦が大きくなるので不適である。かかる化合物Q)
におけるEO単位とPO単位の配列状態はブロック共重
合状でもランダム共重合状でもよい。そして共重合物の
全末端は摩擦を小さくするためにアルキル基、特に炭素
数1〜12のアルキル基によってエーテル結合され念も
のである必要がある。これが一部分の末端封鎖や未封鎖
である場合には、摩擦が大きいという欠点があるので不
適である。封鎖しているアルキル基の好ましい具体例と
しては、メチル基、エチル基、プロピル基、ブチル基な
どが挙げられる。また化合物■の一原料となる多価アル
コールの具体例としては、グリセリン、テトラメチレン
グリコール、ペンタエリスリトール、ソルビトールなど
が挙げらnる。−価のアルコールは平滑性の点で不適で
ある。そして化合物■の配合量は、ヒーター汚れの点で
30〜70重tチが好ましい。もちろん、化合物■とし
て、1種の化合物を単独で用いても、また2種以上の化
合物を併用してもよい。■Ethylene oxide (aO) and propylene oxide (PO) are copolymerized into polyhydric alcohol! 9 is added in a random copolymerized manner, the PO/EO (molar ratio) is 40/60 to 90/10, and substantially all terminals are blocked by ether bonds with alkyl groups having 1 to 12 carbon atoms. and has a molecular weight of 1000 to 5000
30 to 70 weights of a compound (polytetramethylene glycol to ethylene oxy)
"(EO) Tobropyre/oxide (PO) is added in a random copolymerized manner, the PO/EO (mole ratio) is 20/80 to 80/20, and the molecular weight is 250.
Ethylene oxide (EO) and propylene oxide (PO) are added to the polyhydric alcohol in a random copolymerized manner, and the PO/EO (molar ratio) is 20 to 60 times the compound with a molecular weight of 0 to 10,000. /80~80/
Compounds t-2 to 20, which are not substantially end-blocked and have a molecular weight of 1sooo to 28,000
10 times 1 inch, the following are the constituent components of the present invention:
I will explain its role and the basis for specifying it. First, all terminal groups of the component are blocked by alkyl groups, which improves the smoothness of the yarn and prevents fuzz and breakage during high-speed friction false twisting. It is possible to reduce the number of yarns, reduce the number of abnormal crimps, and obtain a processed yarn with fewer lines in knitted fabrics and lines in woven fabrics. Also, there is very little dirt on the heater, which is good. Here, PO/EO (molar ratio) is 40/
The reason for setting the ratio to 60 to 90/10 is to reduce contamination of the heater. If the molecular weight of the compound (1) is less than 1,000, it is preferable in terms of fluid lubricity such as friction against metals, but it is not preferable because it has poor thermal stability and deteriorates rubber swelling properties. On the other hand, if the molecular weight exceeds 5000, friction will increase, which is unsuitable. Such compounds Q)
The arrangement state of the EO units and PO units in may be a block copolymer or a random copolymer. All terminals of the copolymer must be ether bonded by alkyl groups, particularly alkyl groups having 1 to 12 carbon atoms, in order to reduce friction. It is not suitable if the ends are partially closed or unblocked, as they have the drawback of high friction. Preferred specific examples of the blocking alkyl group include methyl group, ethyl group, propyl group, butyl group, and the like. Further, specific examples of the polyhydric alcohol which is a raw material for compound (1) include glycerin, tetramethylene glycol, pentaerythritol, and sorbitol. -hydric alcohols are unsuitable in terms of smoothness. The amount of compound (1) to be blended is preferably 30 to 70 weights in terms of heater stains. Of course, as compound (2), one type of compound may be used alone, or two or more types of compounds may be used in combination.
次に成分(→は、油膜全強化して糸表面を保護する働き
があり、高速摩擦仮撚の際の毛羽を防止する上で著しい
効果を示す。その配合量は20〜600〜60重量%ば
ならず、60重量%を越える場合には、ポリエステル未
延伸フィラメントヲ紡糸倦取る際に繊維間の静摩擦係数
が極端に低くなり棒形状が不良となり、高速摩擦仮撚時
の断糸の原因となる。より好壕しくは、上記■の化合物
の添加量より少量である場合である。(→の化合物にお
いて、エチレンオキサイド(EO)単位とプロピレンオ
キサイド(PO )単位はランダム共重合状で結合さn
ている必要があり、ブロック共重合状で付加されている
場合には、平滑性が不良となる。またPO/go (モ
ル比)は、20/80〜80/20であらねばならず、
この範囲を外れると加工糸毛羽の発生が多くなり好まし
くない。この化合物@の一原叫となるポリテトラメチレ
ングリコールは、分子量500〜300Qの範囲内であ
るのがP O/E Oとのバランスおよび平滑性などの
点で好ましい。Next, the component (→ has the function of completely strengthening the oil film and protecting the yarn surface, and shows a remarkable effect in preventing fuzz during high-speed friction false twisting. Its blending amount is 20 to 600 to 60% by weight. However, if it exceeds 60% by weight, the coefficient of static friction between the fibers becomes extremely low when undrawn polyester filaments are spun, resulting in poor rod shape and causing yarn breakage during high-speed friction false twisting. More preferably, the amount added is smaller than the amount of the compound (①) added. n
If it is added as a block copolymer, the smoothness will be poor. Also, PO/go (molar ratio) must be between 20/80 and 80/20,
If it is out of this range, it is not preferable because processed yarn fuzz will increase. Polytetramethylene glycol, which is the main ingredient of this compound, preferably has a molecular weight in the range of 500 to 300Q from the viewpoint of balance with P O/E O and smoothness.
また化合物(→の分子量は、2500〜10000の範
囲にあるものが効果の点で好虜しく、2500未満のも
のは加工糸毛羽の発生の点で、また10000を4える
ものはポリエステル未延伸フィラメントの棒形状不良の
点で、共に本発明には適さない。In addition, compounds (→) with a molecular weight in the range of 2,500 to 10,000 are preferable in terms of effectiveness, those with a molecular weight of less than 2,500 are preferable in terms of the generation of processed yarn fuzz, and those with a molecular weight of 4 over 10,000 are preferable for undrawn polyester filaments. Both of them are not suitable for the present invention because of their poor rod shape.
次に化合物0は、高速摩擦仮撚における油膜強化によっ
て−1110毛羽防止効果を得る念めに用いるものであ
って、その配合量を2〜10重量%と(7たのは、こn
pt−ヒ配合するとポリエステル未延伸フィラメント
を紡糸・捲取る際に静摩擦係数が極端に低くなり棒形状
が不良となる次めであり、また高速摩擦仮撚時の断糸の
原因にもなるためである。EO単位とPO単位の結合状
態をランダム共重合状に限定し次理由は、前記@の化合
物の場合と同様である。PO/EO(モル比)の限定理
由も前記(Φの場合と同様である。末端は実質的に未封
鎖の状態であることが必須であるが、末端が多く封鎖さ
れている場合には、毛羽防止効果が十分得られない。化
合物■の分子量は18000〜28000の範囲にある
ものが効果の点で好ましく、18000未満のものは加
工糸毛羽発生の点で、また28000を越えるものはポ
リエステルフィラメント棒形状不良の点で、共に本発明
の目的を達成し得ない。Next, Compound 0 is used to ensure that -1110 fluff is prevented by strengthening the oil film during high-speed friction false twisting, and its blending amount is 2 to 10% by weight (7).
This is because when pt-hi is blended, the static friction coefficient becomes extremely low when spinning and winding polyester undrawn filaments, resulting in poor rod shape, and also causes yarn breakage during high-speed friction false twisting. . The bonding state of the EO unit and PO unit is limited to random copolymerization for the same reasons as in the case of the @ compound. The reason for limiting the PO/EO (molar ratio) is the same as in the case of (Φ) above. It is essential that the terminals are substantially unblocked, but if a large number of terminals are blocked, A sufficient anti-fuzz effect cannot be obtained. The molecular weight of compound (1) is preferably in the range of 18,000 to 28,000 from the viewpoint of effectiveness. If it is less than 18,000, it may cause fuzz in the processed yarn, and if it exceeds 28,000, it may be used for polyester filament. In both cases, the object of the present invention cannot be achieved due to the poor shape of the rod.
この化合物■の一原料となる多価アルコールの具体例と
しては、前記■の場合と同様のものが挙げられる。Specific examples of the polyhydric alcohol that is a raw material for compound (1) include the same ones as in the case of (2) above.
本発明は、かかる化合物■〜Oからなる油剤を未延伸糸
に0.3〜0.8俤程度寸与することによって高速摩擦
仮撚で毛羽の発生セト折糸の発生が少なく、捲縮異常が
なく、ニット編地の4没や織物布地の筋発生のない均斉
な加工糸が得られる。In the present invention, by applying approximately 0.3 to 0.8 degrees of an oil agent consisting of such compounds (1 to 0) to undrawn yarn, high-speed frictional false twisting reduces the occurrence of fuzz and set folded yarn, resulting in abnormal crimping. It is possible to obtain a uniformly processed yarn without any creases in knitted fabrics or streaks in woven fabrics.
なお本発明の油剤に、帯電防Iヒの次めに一般的に知ら
れているアルキルスルホネー ト塩やアルキルホスフエ
ート塩を配合しても差支えない。また、さらにIfrた
な効果を得るために、他の油剤単位や改質剤などを上記
本発明油剤に配合してもよい。In addition, the oil agent of the present invention may be blended with an alkyl sulfonate salt or an alkyl phosphate salt, which are generally known next to antistatic agents. Further, in order to obtain further effects such as Ifr, other oil units, modifiers, etc. may be added to the oil agent of the present invention.
本発明は前述した化合物■〜0を用いるものであり、こ
nにより前述したような効果が得られることとなる。従
来より延伸時または仮撚時にヒーター上にタール状物や
スラッジ残渣(スカムと称す)が堆積し、これが原因で
毛羽や断糸が発生しこf′L′t−防ぐ目的で各種化合
物を油剤に添00することが提案されて吟るが、本発明
の■〜(0からなる油剤の場合には、それだけでタール
状物やスカムの堆fjtを防上することができ、あえて
そのような化合物を添hgする必要がない。しかし、必
要によっては、より−1の効果あるいは新たな効果を得
ることを目的として、そのような化合物を添加してもよ
い。The present invention uses the above-mentioned compounds 1 to 0, and the above-mentioned effects can be obtained by using the compounds 1 to 0. Conventionally, various compounds have been used to prevent tar-like substances and sludge residue (called scum) from accumulating on the heater during stretching or false twisting, which causes fluff and yarn breakage. However, in the case of the oil agent of the present invention consisting of It is not necessary to add a compound.However, if necessary, such a compound may be added for the purpose of obtaining a more -1 effect or a new effect.
本発明の上述の油剤は本発明以外の目的、念とえはスピ
ンドル式仮撚)10工原糸処理剤や合成繊維の紡糸、延
伸用原糸処理剤として使用しても一応の効果はある。The above-mentioned oil agent of the present invention can be used for purposes other than the present invention, for example, as a yarn treatment agent for spindle-type false twisting) or a yarn treatment agent for spinning and drawing of synthetic fibers. .
以下に実施例と比較例により本発明全説明する。The present invention will be fully explained below with reference to Examples and Comparative Examples.
実施例1〜4および比較例1〜6
常法によりポリエチレンテレフタレート13200m/
分の紡糸速度で紡糸し、その際に第1表に示す10種の
油剤組成物A、Jをそれぞれ該紡糸原糸に対して油剤付
着量が0.45重盾係となるように付与した。得られた
それぞれの紡糸;工に糸(116デニール/72フイラ
メント)ヲウレタンゴムディスク金備えた牽擦仮撚機を
用いて延伸倍率1.6倍、ヒーター温度210℃、加工
速度6001Tl/分で延伸しながら摩擦仮撚を行なっ
た。そ几ぞ11の紡糸原糸に対して20日間ずつ連続運
転を行ない延伸仮撚性(毛羽、断糸、ヒーター汚れ、捲
縮性等)を調べると共に、得られた仮撚加工糸を編物と
して染色仕上し、4段発生状況を調べた。その晴果を第
1表に示す。第1表に示すA〜、Iの油剤のうちでA、
Dが代表的な本発明油剤であす、E(1) 油剤A、
B、 C,Dは本発明油剤であって、仮撚糸毛羽の発
生及び仮撚断糸の発生が少なく、ヒーター汚れは殆んど
なく、捲縮性及び編物にした際の線膜もなく良好な結果
が得ら′i″Lfc0(2) 油剤Eは全末端封鎖し
友ポリエーテルを主体にし友ものであるが、本発明の@
およびOに対応する化合物を使用していないため加工糸
毛羽が隠めて多く発生している。Examples 1 to 4 and Comparative Examples 1 to 6 Polyethylene terephthalate 13200m/
At this time, 10 types of oil compositions A and J shown in Table 1 were applied to the spun yarn so that the amount of oil applied was 0.45 times. . Each of the obtained fibers was spun: yarn (116 denier/72 filaments) was drawn using a drag false twister equipped with a urethane rubber disc at a stretching ratio of 1.6 times, a heater temperature of 210°C, and a processing speed of 6001 Tl/min. Friction false twisting was performed while stretching. The spun yarn of Step 11 was continuously operated for 20 days each to examine the drawing false twisting properties (fuzz, yarn breakage, heater stains, crimpability, etc.), and the resulting false twisted yarn was used as a knitted fabric. It was dyed and finished, and the occurrence of four stages was examined. The results are shown in Table 1. Among the oils A to I shown in Table 1, A,
D is a typical oil agent of the present invention, E (1) oil agent A,
B, C, and D are oil agents of the present invention, which have little occurrence of false twist yarn fluff and false twist breakage, almost no heater stains, and good crimpability and no line film when knitted. A good result was obtained.'i''Lfc0(2) Oil agent E has all terminals blocked and is mainly composed of polyether, but the @ of the present invention
Since a compound corresponding to O is not used, a large amount of processed yarn fluff is hidden.
(8)油剤Fは本発明で言う■に対応する化合物が用い
られておらず、末端未封鎖ポリエーテルを主体としたも
のであり、(→に対応する化合物も用いられていない。(8) The oil agent F does not contain the compound corresponding to (1) in the present invention, is mainly composed of terminal-unblocked polyether, and also does not contain the compound corresponding to (→).
この1合には、加工糸毛羽は上記Eの油剤よりは減少し
たものの、まだ多く発生し、断糸の発生、スカムの堆積
も非常に多かった。In this first case, although the amount of fuzz on the processed yarn was reduced compared to the oil agent E, a large amount was still generated, and there were also a large number of yarn breaks and scum accumulation.
(4)油剤Gは■に対応する化合物を配合していない場
合であるが、この場合には、平滑性不足のために仮撚毛
羽の発生訃よび仮撚断糸がやや多くγつた0
5) 油剤Hは本発明の0の化合物に対応する化合物を
使用していない場合である。この場合には加工糸毛羽及
び仮撚断糸がやや多く発生している0
(6)油剤工はのの化合物を使用しなかった場合であり
、リロエ糸毛羽が多く発生している。(4) Oil agent G does not contain the compound corresponding to (■), but in this case, due to insufficient smoothness, false twist fuzzing and false twist breakage were slightly more likely to occur. ) Oil agent H does not contain a compound corresponding to compound 0 of the present invention. In this case, a rather large amount of processed yarn fuzz and false-twisted broken yarn occurred. (6) This is the case where the oil processing compound was not used, and a large amount of reloye yarn fuzz occurred.
(γ)油剤Jは■の化合物の配合量が少なすぎる場合で
あり、ヒーター汚れが短時間で発生し、仮撚断糸及び加
工糸毛羽がヒーター汚れと共に急激に増加し念。仮撚開
始当初は加工糸毛羽及び仮撚断糸並びに捲縮性及び編地
の4段ば良好であったが、ヒーター汚れの増加と共に捲
縮性が悪化し、編地の4段や織物の筋が発生した。また
ゴム1彫潤性が劣った。(γ) Oil agent J is a case where the compounding amount of the compound (■) is too small, and heater stains occur in a short period of time, and false-twisted yarn and processed yarn fuzz rapidly increase along with heater stains. At the beginning of false twisting, the processed yarn fuzz, the false twisted broken yarn, the crimpability, and the 4th row of the knitted fabric were good, but as the heater dirt increased, the crimpability deteriorated, and the 4th row of the knitted fabric and the 4th row of the knitted fabric were good. Streaks occurred. Furthermore, the engraving properties of Rubber 1 were poor.
以下余日Remaining days below
Claims (1)
プロピレンオキサイド(PO)がブロック共重合状にま
たはランダム共重合状に付加されており、PO/EO(
モル比)が40/60〜90/10であつて、実質的に
全ての末端が炭素数1〜12のアルキル基によつてエー
テル結合封鎖されており、かつ分子量が1000〜50
00である化合物を30〜70重量%、 [ロ]ポリテトラメチレングリコールにエチレンオキサ
イド(EO)とプロピレンオキサイド(PO)がランダ
ム共重合状に付加されており、PO/EO(モル比)が
20/80〜80/20であつて、かつ分子量が250
0〜10000である化合物を20〜60重量%、 [ハ]多価アルコールにエチレンオキサイド(EO)と
プロピレンオキサイド(PO)がランダム共重合状に付
加されており、PO/EO(モル比)が20/80〜8
0/20であつて、実質的に末端が封鎖されておらず、
かつ分子量が18000〜28000である化合物を2
〜10重量%、からなることを特徴とする高速摩擦仮撚
に好適な油剤。[Scope of Claims] Constituent components and constituent ratios of the following [a] to [c] [a] Ethylene oxide (EO) and propylene oxide (PO) are block copolymerized or random copolymerized in a polyhydric alcohol It is added and PO/EO (
molar ratio) is 40/60 to 90/10, substantially all terminals are blocked by ether bonds with alkyl groups having 1 to 12 carbon atoms, and the molecular weight is 1000 to 50.
Ethylene oxide (EO) and propylene oxide (PO) are added to polytetramethylene glycol in a random copolymerized manner, and the PO/EO (molar ratio) is 20 to 70% by weight. /80 to 80/20 and has a molecular weight of 250
20 to 60% by weight of a compound having a molecular weight of 0 to 10,000; 20/80-8
0/20, the end is not substantially blocked,
and a compound having a molecular weight of 18,000 to 28,000.
~10% by weight, an oil agent suitable for high-speed friction false twisting.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14388688A JPH0291273A (en) | 1988-06-10 | 1988-06-10 | Lubricant suitable for high-speed frictional false-twisting |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14388688A JPH0291273A (en) | 1988-06-10 | 1988-06-10 | Lubricant suitable for high-speed frictional false-twisting |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0291273A true JPH0291273A (en) | 1990-03-30 |
Family
ID=15349314
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP14388688A Pending JPH0291273A (en) | 1988-06-10 | 1988-06-10 | Lubricant suitable for high-speed frictional false-twisting |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0291273A (en) |
-
1988
- 1988-06-10 JP JP14388688A patent/JPH0291273A/en active Pending
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP3188687B2 (en) | Smooth polyester fiber | |
JP3856617B2 (en) | False twisting polyester fiber | |
JPH11229276A (en) | Polyester fiber having excellent processability | |
JP2703620B2 (en) | Manufacturing method of polyester false twisted yarn | |
JPH01306684A (en) | Oiling agent suitable for high-speed friction false twisting | |
JPH0291273A (en) | Lubricant suitable for high-speed frictional false-twisting | |
JPS6225789B2 (en) | ||
JPH0284573A (en) | Oiling agent suitable for high-speed friction false twisting | |
JPS6247992B2 (en) | ||
JPH0434088A (en) | Finishing oil composition | |
JPS6075676A (en) | Oil agent for friction false twisting | |
JP2005029936A (en) | Polyester-based conjugate fiber | |
JPH0127195B2 (en) | ||
JP3909265B2 (en) | Method for drawing false twist of synthetic fiber | |
JPH04126875A (en) | Treating agent for synthetic fiber | |
JP3420086B2 (en) | Synthetic fiber drawing false twist method | |
JPH04281071A (en) | Production of polyester fiber | |
JPS61167081A (en) | Oil agent for friction false twisting | |
JP2003306869A (en) | Oil for friction false twisting of synthetic fiber | |
JPS6359483A (en) | Raw yarn for high speed stretching friction false twisting processing and method for false twisting of said raw yarn | |
JPH0346586B2 (en) | ||
JP3720162B2 (en) | Treatment agent for synthetic fibers | |
JP2000345473A (en) | Synthetic yarn for false twisting | |
JP2007262588A (en) | Multifilament yarn for microfiber | |
JPH03871A (en) | Textile-treating agent |