JPH0284573A - Oiling agent suitable for high-speed friction false twisting - Google Patents
Oiling agent suitable for high-speed friction false twistingInfo
- Publication number
- JPH0284573A JPH0284573A JP14388788A JP14388788A JPH0284573A JP H0284573 A JPH0284573 A JP H0284573A JP 14388788 A JP14388788 A JP 14388788A JP 14388788 A JP14388788 A JP 14388788A JP H0284573 A JPH0284573 A JP H0284573A
- Authority
- JP
- Japan
- Prior art keywords
- molecular weight
- yarn
- molar ratio
- compound
- weight
- 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
- 239000008041 oiling agent Substances 0.000 title abstract 3
- 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 24
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims abstract description 21
- -1 fatty acid ester Chemical class 0.000 claims abstract description 12
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 6
- 229930195729 fatty acid Natural products 0.000 claims abstract description 6
- 239000000194 fatty acid Substances 0.000 claims abstract description 6
- 150000005846 sugar alcohols Polymers 0.000 claims abstract description 6
- 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
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 8
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 4
- 239000000470 constituent Substances 0.000 claims description 3
- 238000007334 copolymerization reaction Methods 0.000 claims description 3
- 238000012661 block copolymerization Methods 0.000 claims description 2
- 239000004721 Polyphenylene oxide Substances 0.000 abstract description 8
- 229920000570 polyether Polymers 0.000 abstract description 8
- 238000002156 mixing Methods 0.000 abstract description 2
- 229920005604 random copolymer Polymers 0.000 abstract 3
- 229920001400 block copolymer Polymers 0.000 abstract 1
- 238000009941 weaving Methods 0.000 abstract 1
- 239000003921 oil Substances 0.000 description 30
- 238000000034 method Methods 0.000 description 11
- 239000004744 fabric Substances 0.000 description 8
- 230000000694 effects Effects 0.000 description 7
- 239000000835 fiber Substances 0.000 description 6
- 229920000728 polyester Polymers 0.000 description 6
- 238000009987 spinning Methods 0.000 description 5
- 238000004804 winding Methods 0.000 description 5
- 239000002759 woven fabric Substances 0.000 description 5
- 230000002159 abnormal effect Effects 0.000 description 4
- 238000011109 contamination Methods 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 3
- 238000002788 crimping Methods 0.000 description 3
- 239000000314 lubricant Substances 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- 230000003068 static effect Effects 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
- 230000007547 defect Effects 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 2
- 239000010931 gold Substances 0.000 description 2
- 229910052737 gold Inorganic materials 0.000 description 2
- 239000010802 sludge Substances 0.000 description 2
- 238000005728 strengthening Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 230000002522 swelling effect Effects 0.000 description 2
- GFVYDNHWTCHDSN-UHFFFAOYSA-N 14-methylpentadecyl octanoate Chemical compound CCCCCCCC(=O)OCCCCCCCCCCCCCC(C)C GFVYDNHWTCHDSN-UHFFFAOYSA-N 0.000 description 1
- MLMNMIJAOFTZNN-UHFFFAOYSA-N 16-methylheptadecyl hexanoate Chemical compound CCCCCC(=O)OCCCCCCCCCCCCCCCC(C)C MLMNMIJAOFTZNN-UHFFFAOYSA-N 0.000 description 1
- MVUWRLHKGKEGSS-UHFFFAOYSA-N 16-methylheptadecyl octanoate Chemical compound CCCCCCCC(=O)OCCCCCCCCCCCCCCCC(C)C MVUWRLHKGKEGSS-UHFFFAOYSA-N 0.000 description 1
- 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
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- 229920006311 Urethane elastomer Polymers 0.000 description 1
- WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 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
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 230000005611 electricity Effects 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
- 238000009730 filament winding Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 238000009940 knitting Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000002480 mineral oil Substances 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
- 230000002265 prevention Effects 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
- 238000010186 staining Methods 0.000 description 1
- 125000005480 straight-chain fatty acid group Chemical group 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
Landscapes
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
Description
【発明の詳細な説明】
〈産業上の利用分野〉
本沼明は、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11次ニット編地や織物布地を提供し得る加工糸
製造用油剤、特に高速延伸仮撚用油剤に関するものであ
る。[Detailed Description of the Invention] <Industrial Field of Application> Akira Motonuma 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. The present invention relates to a lubricant for producing textured yarn, which can provide excellent uniformity of 11th order knitted fabrics and woven fabrics without any observed defects, and in particular to a lubricant for high-speed stretching and false twisting.
〈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
糸後の未延伸糸を一旦延伸糸とし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次は連続的に行なう
方法がアリ、最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。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憲靜仮撚方法が採用
されており、特に4擦仮撚方式の採用によってJJロエ
速度は400〜1000m/分のように飛躍的に向上し
つつある。<Conventional technology> Conventionally, methods for obtaining processed yarns of polyester fibers include a method in which undrawn yarn after spinning is first turned into a drawn yarn and then false-twisted, and a method in which drawing and false-twisting are simultaneously or continuously performed from the spun raw yarn. However, due to recent advances in technology, the latter method of simultaneous stretching and false twisting has become the main method. The spindle false-twisting method and the Kensei false-twisting method have been adopted as methods for applying such stretch false-twisting, and in particular, by adopting the 4-flip false-twisting method, the JJ loe speed has been dramatically improved to 400 to 1000 m/min. It is being done.
〈発明が解決しようとする課題〉
しかし加工速度のト昇eこ伴って、糸と各樵接触体(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几る。<Problem to be solved by the invention> However, as the processing speed increases, the friction between the yarn and each woodcutter contact body (e.g. guide, roller heater) increases, causing damage to the fibers, causing fuzz and yarn breakage. The disadvantage is that the number of occurrences increases.
ま之一方で、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n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発生の原因となり、ニット
編地の線膜や織物布地に筋などが発生する。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。However, due to the increased false-twisting speed, conventional false-twisting oils can significantly contaminate the heater and, in extreme cases, cause tar build-up and sludge residue (hereinafter referred to as scum) to build up on the heater. However, this causes an increase in the occurrence of fuzz and yarn breakage in the processed yarn. Furthermore,
This causes abnormal crimping and dyeing spots, and streaks appear on knitted fabrics and 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じ九油剤が種々提案されている。Recently, heat-resistant oils have been studied, and various oils have been proposed, one of which is mainly composed of polyether compounds.
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
たポリエステルマルチフィラメント糸を延伸同時仮撚を
行なうと、ヒーター汚れに対しては良好な結果が得られ
、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まりつつある
。このような細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、ま念得られ念加工糸の毛羽も多くなる。When polyester multifilament yarns coated with an oil agent containing polyether as a main component are drawn and false-twisted at the same time, good results are obtained against heater stains and effective in preventing yarn breakage and fluffing. ing. 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 an increasing demand for finer denier crimped yarns. When obtaining such fine denier textured yarn under high-speed frictional false twisting, if the above-mentioned polyether-based oil agent is used, heater fouling will worsen and yarn breakage will increase over time, making it difficult to obtain There will also be more fluff in the yarn that has been processed.
このために、単繊維デニールが1.2デニール以下であ
る細デニール糸を加工速度500m/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難しく不可能
に近い状態であった。For this reason, it is extremely difficult and nearly impossible to produce fine denier yarn with a single fiber denier of 1.2 denier or less using high-speed friction false twisting at a processing speed of 500 m/min or higher. .
〈課題を解決する友めの手段〉
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九る本発明油剤に到達し次もので
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1行なう
に際して、前述しtような種々の弊害をも之らさないと
ころの高速摩擦仮撚用油剤を提供するものである。<Friendly Means to Solve 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 contamination, less fuzzing, less occurrence of yarn breakage, and even less crimping. As a result of the present invention, it is possible to obtain a processed yarn with uniform properties and without the formation of a line film. 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 suffer from the various disadvantages mentioned above when performing high-speed friction false-twisting at a speed 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tよう
な欠点を防止する念めに、下記■〜■の成分を配合し念
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, the following components (1) to (4) are blended and a lubricant is used.
■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 )がブロック共重合状にま九
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1000〜500
0である化合物を30〜70重量tチ、
■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/a。■ Ethylene oxide (EO) and propylene oxide (PO) are added to polyhydric alcohol in a block copolymerized manner, and Maku is added in a random copolymerized manner, with a PO/EO (mole ratio) of 40/60 to 90/10. , substantially all of the terminals are blocked by ether bonds with alkyl groups having 1 to 12 carbon atoms, and the molecular weight is 1000 to 500.
30 to 70 weight tons of a compound with a polytetramethylene glycol (po/a), which is a polytetramethylene glycol in which ethylene oxide (EO) and propylene oxide (PO) are randomly copolymerized.
(モル比)が20/80〜80/20であって、かつ分
子量が2500〜10000である化合物を20〜60
重量%、
■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nておらず、かつ
分子量が18000〜28000である化合物を2〜1
0重量%、075℃における粘度が2〜5セ/チボイズ
である分岐脂肪酸エステルを4〜15重量%、以下に本
発明の構成成分■〜■について、そしてその役割とそれ
全特定した根拠について説明する0
まず成分■は、全末端基をアルキル基により封鎖されて
おり、こnにより糸の平滑性金より向上させ、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nる。ま九ヒーター汚れも非常に少
なく良好である。ここでP(J/EO(モル比)金40
/60〜90/10とした理由は、ヒーター汚れを少な
くするためである。ま之化合物■の分子量が1000未
溝の場合には、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5000を越え
ると摩擦が大きくなるので不適である。かかる化合物■
におけるEO単位とPO年単位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念めにアルキル基、特に炭素
数1〜12のアルキル基によってエーテル結合さntも
のである必要がある。こn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。ま九化合物■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、ペンタエリスリ
トール、ソルビトール、トリメチロールプロパンなどが
挙げら≠
れる。−価のアルコールは・滑性不良の点で不適である
。そして化合物■の配合量は、ヒーター汚れおよび平滑
性の点で30〜70重量%が好ましい。(molar ratio) of 20/80 to 80/20 and a molecular weight of 2,500 to 10,000.
Weight%, ■ Ethylene oxide (EO) and propylene oxide (PO) are added to polyhydric alcohol in a random copolymerized manner, and the PO/EO (molar ratio) is 20/80 to 80/
20, which is not substantially end-blocked, and has a molecular weight of 18,000 to 28,000.
0% by weight, 4 to 15% by weight of branched fatty acid ester with a viscosity of 2 to 5 centimeters/cm at 075°C. Below, the constituent components of the present invention (■ to ■), their roles, and the basis for specifying them will be explained. 0 First, component (2) has all terminal groups blocked by alkyl groups, which improves the smoothness of the yarn compared to gold, reduces fuzz and yarn breakage during high-speed friction false twisting, and also prevents abnormal crimping. It is possible to obtain a processed yarn with less generation of lines in knitted fabrics and lines in woven fabrics. The heater is in good condition with very little dirt. Here, P (J/EO (mole ratio)) gold 40
The reason for setting the ratio to be /60 to 90/10 is to reduce heater contamination. If the molecular weight of the compound (2) is less than 1000, it is preferable in terms of fluid lubricity such as friction against metal, 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 5,000, friction will increase, which is unsuitable. Such compounds■
The arrangement state of the EO units and PO units in may be block copolymerized or random copolymerized. All terminal ends 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 unsuitable if the terminal is partially blocked or unblocked, as this has 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. Specific examples of polyhydric alcohols that can be used as raw materials for compound (1) include glycerin, pentaerythritol, sorbitol, trimethylolpropane, and the like. -hydric alcohols are unsuitable due to poor lubricity. The amount of compound (1) to be blended is preferably 30 to 70% by weight in terms of preventing heater stains and smoothness.
もちろん、化合物のとじて、1種の化合物を単種で用い
ても、ま念2種以上の化合物を併用してもよい。Of course, in terms of compounds, one type of compound may be used alone, or two or more types of compounds may be used in combination.
次に成分Oは、油嘆を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20〜60重t%であらねばな
らず、60重を憾を越える場合には、ポリエステル未埋
伸フィラメント?紡糸捲取る際に繊維間の静摩擦係数が
極端に低くなり、捲形状が不良となり、高速摩擦仮撚時
の断糸の原因となる。より好ましくは、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)単位とブaピレンオキ
サイド(PO)単位はランダム共重合状で結合されてい
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/EO(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Dロエ糸毛羽の発生が多くなり好ましくな
い。この化合物@の一原料となるポリテトラメチレング
リコールは、分子量500〜3000の範囲内であるの
がPO/EOとのバランスおよび平滑性などの点で好ま
しい。Next, component O has the function of strengthening the oil tension and protecting the yarn surface, and exhibits a remarkable effect in preventing fuzzing during high-speed friction false twisting. The blending amount must be 20 to 60% by weight, and if it exceeds 60% by weight, it should be polyester unfilled filament. During spinning and winding, the coefficient of static friction between fibers becomes extremely low, resulting in poor winding 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) above. In the compound (2), the ethylene oxide (EO) units and the butyrene oxide (PO) units must be combined in a random copolymerization manner, and if they are added in a block copolymerization manner, the smoothness will be affected. It becomes defective. Also PO/EO (molar ratio)
must be in the range of 20/80 to 80/20, and if it is outside this range, the occurrence of D loe yarn fuzz will increase, which is not preferable. Polytetramethylene glycol, which is a raw material for this compound @, preferably has a molecular weight within the range of 500 to 3000 from the viewpoint of balance with PO/EO and smoothness.
ま念化合物@の分子量は、2500〜10000の範囲
にあるものが効果の点で好ましく、2500未満のもの
は加工糸毛羽の発生の点で、また10000を越えるも
のはポリエステル未延伸フィラメントの捲形状不良の点
で、共に本発明には適さない。The molecular weight of the Manen compound @ is preferably in the range of 2,500 to 10,000 from the viewpoint of effectiveness. If it is less than 2,500, it may cause fuzz in the processed yarn, and if it exceeds 10,000, it may affect the winding shape of the undrawn polyester filament. Both are unsuitable for the present invention due to their defects.
次に化合物■は、高速摩擦仮撚における油膜強化によっ
て一層の毛羽防止効果を得る几めに用いるものであって
、その配合f’r2〜10重量%としたのけ、これ以上
配合するとポリエステル未延伸フィラメントヲ紡糸・捲
取る際に静摩擦係数が極端に低くなり捲形状が不良とな
るためであり、ま念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年単位結合状態をランダ
ム共重合状に限定した理由は、前記O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@
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。化合物のの分子
f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、ま念28000を越えるものはポリエステルフ
ィラメント捲形状不良の点で、共に本発明の目的を達成
し得ない。Next, compound (1) is used to further prevent fuzzing by strengthening the oil film during high-speed friction false twisting. This is because when spinning and winding the drawn filament, the coefficient of static friction becomes extremely low, resulting in a poor winding shape, and also causes yarn breakage during high-speed friction false twisting. The reason why the bonding state of the EO unit and the PO unit is limited to a random copolymerization state is the same as in the case of the O compound. The reason for limiting PO/EO (molar ratio) is also mentioned above.
The same is true for . It is essential that the ends are substantially unblocked, but if the ends are blocked too much, a sufficient fuzz-preventing effect cannot be obtained. It is preferable that the molecule f of the compound is in the range of 18,000 to 28,000 from the viewpoint of effectiveness.If it is less than 18,000, it will cause fuzz in the processed yarn, and if it exceeds 28,000, it will cause poor polyester filament winding shape. In both cases, the purpose of the present invention cannot be achieved.
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.
化合物■は、上記■〜■のポリエーテル系化合物のみで
は糸に対する平滑性が充分でなく、高速摩擦仮撚での毛
羽防止および捲縮異常によるニット編地の線膜や織物布
地の筋発生などを完全に防止することが不可能であるこ
とより用いるものである。この分岐脂肪酸エステルを添
加することによるヒーター汚れ防止効果は、前記■〜○
のポリエーテル系化合物と同程度で非常に良好である。Compound (■) does not provide sufficient smoothness to the yarn when using only the polyether compounds (■ to ■) above, and prevents fuzzing during high-speed friction false twisting and causes lines in knitted fabrics and streaks in woven fabrics due to abnormal crimp. It is used because it is impossible to completely prevent this. The heater stain prevention effect by adding this branched fatty acid ester is as follows
It is very good, being on the same level as polyether compounds.
従来一般に使用されている鉱物油や直鎖型脂肪酸エステ
ルではヒーター汚nが激しい。化合物■の75℃におけ
る粘度が2センチポイズ未満である場合には、平滑性は
良好であるが、高温での集束性が不良となる。その一方
、粘度が5センチポイズを越える場合には、ヒーター汚
れをきたし、好ましくない。この分岐脂防酸エステルは
、一般にオキソ法によって得らnた炭素数12〜18の
分岐鎖アルコールと炭素数1〜8の低級カルボン酸より
なる合成エステルを代表とする。本発明の分岐脂肪酸エ
ステルの好ましい例としては、インステアリルアジペー
ト、イソステアリルヘキサネート、イソステアリルオク
タネート、イソヘキサデシルオクタネート等が挙げられ
る。化合物■の配合量は、平滑性およびヒーター汚れの
点で5〜30重量%が好ましい。Mineral oils and straight chain fatty acid esters that have been commonly used in the past cause severe heater contamination. When the viscosity of compound (1) at 75° C. is less than 2 centipoise, the smoothness is good, but the cohesiveness at high temperatures is poor. On the other hand, if the viscosity exceeds 5 centipoise, the heater will become contaminated, which is not preferable. The branched fatty acid-protecting ester is typically a synthetic ester consisting of a branched alcohol having 12 to 18 carbon atoms and a lower carboxylic acid having 1 to 8 carbon atoms, which is generally obtained by the oxo method. Preferred examples of the branched fatty acid ester of the present invention include instearyl adipate, isostearyl hexanate, isostearyl octanate, isohexadecyloctanate, and the like. The amount of compound (1) to be blended is preferably 5 to 30% by weight in terms of smoothness and heater staining.
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多種度付与することによって高速摩擦
仮撚で毛羽の発生や断糸の発生が少なく、捲縮異常がな
く、ニット編地の線膜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 an oil agent consisting of such compounds (1) to (0) to undrawn yarn in a degree of variation of 0.3 to 0.8, the occurrence of fuzz and yarn breakage is reduced during high-speed friction false twisting, and abnormal crimp is prevented. It is possible to obtain a uniformly processed yarn without lines in knitted fabrics or streaks in woven fabrics.
なお本発明の油剤に、帯電防止の念めに一般的ニ知うれ
ているアルキルスルホネート塩やアルキルホスフェート
塩を配合しても差支えない。またさらに新たな効果を得
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。It should be noted that the oil agent of the present invention may be blended with a commonly known alkyl sulfonate salt or alkyl phosphate salt in order to prevent static electricity. Furthermore, in order to obtain new effects, other oil units, modifiers, etc. may be added to the oil agent of the present invention.
本発明は前述し九化合物■〜■を用いるものであり、こ
れにより前述しtような効果が得らnることとなる。従
来より延伸時ま次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、これを防ぐ目的で各種化合物を油
剤に添加することが提案されているが、本発明の■〜■
からなる油剤の場合には、それだけで十分にタール状物
やスカムの堆積を防止することができ、あえてそのよう
な化合物を添加する必要がない。しかし、必要によって
は、より一層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 nine compounds (1) to (2) described above, and thereby the effects as described above can be obtained. Traditionally, tar-like substances and sludge residue (called scum) accumulate on the heater during stretching and false twisting, which causes fluff and yarn breakage, and various compounds are added to the oil agent to prevent this. Although it is proposed to do so, ■~■ of the present invention
In the case of an oil agent consisting of, it is sufficient to prevent the accumulation of tar-like substances and scum, and there is no need to add such compounds. However, if necessary, such compounds may be added for the purpose of obtaining further effects or new effects.
本発明の上述の油剤は本発明以外の目的、九とえばスピ
ンドル式仮撚加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, such as as a yarn treatment agent for spindle type false twist processing, spinning of synthetic fibers, and yarn treatment agent for drawing.
以下に実施例と比較例により本発明を説明する。The present invention will be 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e3200m/
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tSとなるように付与しto得られ九
それぞれの紡糸原糸(116デニー/L//72フイラ
メント)ヲウレタンゴムディスクを備え念摩擦仮撚機を
用いて延伸倍率1.6倍、ヒーター温度210℃、加工
速度600m/分で延伸しながら摩擦仮撚を行なつto
それぞれ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f’L7を仮撚加工糸を編物
として染色仕上し、線膜発生状況を調べた。その結果を
第1表に示す。第1表に示すA、Jの油剤のうちでA〜
Dが代表的な本発明油剤であり、E〜Jは比較例の油剤
である。Examples 1-4 and Comparative Examples 1-6 Polyethylene terephthalate e3200m/
At this time, ten types of oil compositions A and J shown in Table 1 were applied to the spun yarn so that the amount of oil adhesion was 0.45 weight tS. The nine obtained spinning yarns (116 dennies/L//72 filaments) were drawn using a friction false twister equipped with a urethane rubber disk at a stretching ratio of 1.6 times, a heater temperature of 210°C, and a processing speed of 600 m/min. Perform friction false twisting while stretching.
Continuous operation was carried out for each spun yarn for 20 days each, and the drawing and false twisting properties (fuzz, yarn breakage, heater stains, crimpability, etc.) were examined, and the resulting f'L7 was knitted with the false twisted yarn. The specimen was dyed and finished, and the development of line membranes was examined. The results are shown in Table 1. Among the oils A and J shown in Table 1, A~
D is a typical oil agent of the present invention, and E to J are oil agents of comparative examples.
以下にこれら実験例の結果について考案する。The results of these experimental examples will be discussed below.
(1) 油剤A、 B、 C,Di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t際の線
膜もなく良好な結果が得られた。(1) Oil agents A, B, C, and Di are oil agents of the present invention, which cause less occurrence of false twist yarn fluff and false twist breakage, almost no heater stains, and improved crimpability and knitting properties. Good results were obtained with no streaks.
(2)油剤Eは全末端封鎖し次ポリエーテルを主体にし
たものであるが、本発明の@および○に対応する化合物
を使用していない九め加工糸毛羽が多く発生している。(2) Oil agent E is all terminal-blocked and is mainly composed of polyether, but many fluffs are generated in the finished yarn, which does not use the compounds corresponding to @ and ○ of the present invention.
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tもの
であり、■および@に対応する化合物も用いらnていな
い。この場合には、加工糸毛羽は上記Eの油剤よりは減
少し比ものの、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。8) Oil agent F does not contain any compound corresponding to (2) in the present invention, is mainly composed of terminal-unblocked polyether, and does not contain any compound corresponding to (2) or @. In this case, although the amount of processed yarn fuzz was reduced compared to that of oil agent E, a large amount still occurred, and occurrence of yarn breakage and accumulation of scum were also very large.
(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、平滑性不足の几めに仮撚毛
羽の発生および仮撚断糸がやや多くなつ之。(4) Oil agent G does not contain the compound corresponding to (2), but in this case, due to the lack of smoothness, the occurrence of false twist fluff and false twist breakage is slightly increased.
(5)油剤Hは本発明の@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Oの化合物を使用しなかつ次場合であり
、加工糸毛羽が多く発生している。(5) Oil agent H does not contain a compound corresponding to the @ compound of the present invention. In this case, slightly more fuzz and false-twisted broken yarn are generated.
(γ) 油剤Jは本発明のOに対応する化合物を使用し
ていないことおよび■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nと共に急激に増加し念。(γ) Oil agent J does not use the compound corresponding to O of the present invention, and the amount of compound (■) is too small, and heater stains occur in a short period of time, causing false twisting (thread breakage and processing). Please note that thread fuzz increases rapidly with heater contamination.
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
び編地の線膜は良好であつ九が、ヒーター汚れの増加と
共に捲縮性が悪化し、絹地の線膜や織物の筋が発生し友
。またゴム膨潤性が劣った。At the beginning of false-twisting, the processed yarn fuzz, the false-twisted broken yarn, the crimpability, and the line film of the knitted fabric were good, but as the heater dirt increased, the crimp property deteriorated, and the line film of the silk fabric and the line film of the fabric were good. A friend that happens. Furthermore, the rubber swelling property was poor.
以下余白Margin below
Claims (1)
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1000〜5000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2500〜10000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%、[ニ]75℃における粘度が2〜5セン
チポイズである分岐脂肪酸エステルを4〜15重量%、
からなることを特徴とする高速摩擦仮撚に適した油剤。[Scope of Claims] Constituent components and constituent ratios of the following [a] to [d] "a" polyhydric alcohol containing ethylene oxide (EO) and propylene oxide (PO) in a block copolymerization form or a random copolymerization form. 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 5000. % by weight, ethylene oxide (EO) and propylene oxide (PO) are added to polytetramethylene glycol in a random copolymerized manner, and the PO/EO (molar ratio) is 20/80 to 80/20.
and 20 to 60% by weight of a compound having a molecular weight of 2,500 to 10,000; /EO (molar ratio) is 20/80 to 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, [d] 4 to 15% by weight of a branched fatty acid ester having a viscosity of 2 to 5 centipoise at 75°C;
An oil agent suitable for high-speed friction false twisting, characterized by the following:
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14388788A JPH0284573A (en) | 1988-06-10 | 1988-06-10 | Oiling agent suitable for high-speed friction false twisting |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP14388788A JPH0284573A (en) | 1988-06-10 | 1988-06-10 | Oiling agent suitable for high-speed friction false twisting |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0284573A true JPH0284573A (en) | 1990-03-26 |
Family
ID=15349340
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP14388788A Pending JPH0284573A (en) | 1988-06-10 | 1988-06-10 | Oiling agent suitable for high-speed friction false twisting |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0284573A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2010516839A (en) * | 2007-01-17 | 2010-05-20 | ダウ グローバル テクノロジーズ インコーポレイティド | Lubricant composition and method for producing the same |
-
1988
- 1988-06-10 JP JP14388788A patent/JPH0284573A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2010516839A (en) * | 2007-01-17 | 2010-05-20 | ダウ グローバル テクノロジーズ インコーポレイティド | Lubricant composition and method for producing the same |
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