JPS6254910B2 - - Google Patents
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- Publication number
- JPS6254910B2 JPS6254910B2 JP18392783A JP18392783A JPS6254910B2 JP S6254910 B2 JPS6254910 B2 JP S6254910B2 JP 18392783 A JP18392783 A JP 18392783A JP 18392783 A JP18392783 A JP 18392783A JP S6254910 B2 JPS6254910 B2 JP S6254910B2
- Authority
- JP
- Japan
- Prior art keywords
- yarn
- false
- weight
- heater
- twisting
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 150000001875 compounds Chemical class 0.000 claims description 15
- 125000004432 carbon atom Chemical group C* 0.000 claims description 10
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 9
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims description 9
- 229920001296 polysiloxane Polymers 0.000 claims description 7
- 150000003839 salts Chemical class 0.000 claims description 5
- 150000005846 sugar alcohols Polymers 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 3
- 229920001400 block copolymer Polymers 0.000 claims description 2
- 229920005604 random copolymer Polymers 0.000 claims description 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 1
- 239000003921 oil Substances 0.000 description 29
- 239000003795 chemical substances by application Substances 0.000 description 20
- 239000004744 fabric Substances 0.000 description 12
- 239000004721 Polyphenylene oxide Substances 0.000 description 10
- 229920000570 polyether Polymers 0.000 description 10
- 238000000034 method Methods 0.000 description 6
- 239000002759 woven fabric Substances 0.000 description 6
- 238000002156 mixing Methods 0.000 description 5
- 238000012986 modification Methods 0.000 description 5
- 230000004048 modification Effects 0.000 description 5
- 238000012545 processing Methods 0.000 description 5
- -1 and in extreme cases Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000000835 fiber Substances 0.000 description 4
- 229920000728 polyester Polymers 0.000 description 4
- 238000009987 spinning Methods 0.000 description 4
- 230000005856 abnormality Effects 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 150000008052 alkyl sulfonates Chemical class 0.000 description 2
- 150000001734 carboxylic acid salts Chemical class 0.000 description 2
- 150000001735 carboxylic acids Chemical class 0.000 description 2
- 238000011109 contamination Methods 0.000 description 2
- 238000002788 crimping Methods 0.000 description 2
- 238000004043 dyeing Methods 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 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
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 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
- 230000002159 abnormal effect Effects 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000009940 knitting Methods 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000005461 lubrication Methods 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
- 150000002763 monocarboxylic acids Chemical class 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
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 238000005728 strengthening Methods 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
Description
本発明は主としてポリエステル繊維の高速延伸
摩擦仮撚用油剤に関するものであり、より詳しく
は高速延伸摩擦仮撚に際してヒーター汚れがほと
んど観察されず均一な捲縮加工糸として得られ、
均一性の優れたニツト編地や織物布地を提供しう
る加工糸製造用油剤とくに高速延伸仮撚用油剤に
関するものである。
ポリエステル繊維の加工糸を得る方法として
は、紡糸後の未延伸糸をいつたん延伸糸としてか
ら仮撚する方法および最近DTY技術の進歩によ
り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、後者の例が多い。そして、
かかる延伸仮撚付与方法としてはスピンドル仮撚
方法および摩擦仮撚方法が採用されており、とく
に摩擦仮撚方式の採用によつて加工速度は400〜
1000m/分のように飛躍的に向上しつつある。し
かし、加工速度の上昇に伴なつて糸と各種接触体
(たとえばガイド、ローラ、ヒーター)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欠点が現われる。ま
た、一方で仮撚速度の増大により従来よく知られ
ている処理剤ではヒーターが著しく汚染され、極
端な場合にはヒーター上でタール化物、スラツジ
の残査(以後スカムと略称)により加工糸の毛羽
の発生や断糸の発生が増大する。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
ツト編地の緯段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ひんぱ
んに実施しなければならず操業性に乏しい。
最近、耐熱性の油剤が検討されており、その一
つとして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。そして、かかるポリエーテ
ルを主成分とする処理剤を付与したポリエステル
マルチフイラメント糸を高速摩擦仮撚を行なうと
ヒーター汚れに対しては良好な結果が得られる
が、処理時間の経過とともに毛羽の発生や断糸の
発生が多くなつてくる。このことは、捲縮異常の
発生および染色斑の発生の原因となり、ニツト編
地の緯段や織物布地に筋などが発生する。
本発明はこれらの問題点を解決せんとして鋭意
研究の結果、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、また捲縮性の均一な緯段の
ない加工糸が得られることを見出したものであ
る。
すなわち、本発明は複屈折率(Δn)が0.02〜
0.08程度のポリエステル未延伸マルチフイラメン
トを加工速度が数100〜1000m/分のような高速
で摩擦仮撚するに際して、前述のような種々の弊
害を持たらさないところの高速摩擦仮撚用油剤に
関するものである。
本発明の端緒は、高速摩擦仮撚用油剤として用
いられているポリエーテル化合物の有する前述の
ような欠点を防止せんとしたことにあり、この問
題点を解決するために下記の(イ)〜(ハ)成分を配合す
ることで著しい効果を見出した。
(イ) 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)のブロ
ツクまたはランダム共重合物を付加したPO/
EO(モル比)が40/60〜90/10にして、すべ
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た分子量1000〜7000の化
合物1種以上で構成されたものを20〜99重量%
(ロ) 30℃における粘度が100センチポイズ以上の
変性シリコンを0.2〜5重量%
(ハ) 炭素数1〜5のカルボン酸の塩を0.1〜5重
量%
以下に本発明の必須成分(イ)〜(ハ)の役割とそれを
選定した根拠について説明する。
(イ)は、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が減少し、捲縮異常が少なく
なり、ニツト編地の緯段や織物布地の筋の少ない
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。本発明における化合物(イ)の多価
アルコールとしてはソルビタン系またはソルビト
ール系の多価アルコール、ペンタエリスリトール
あるいはトリメチロールプロパン等であつて、化
合物(イ)は当該多価アルコールにエチレンオキサイ
ド(EO)およびプロピレンオキサイド(PO)を
付加したものであり、かかる化合物(イ)の結合状態
はブロツク重合でもランダム重合でもよいが、共
重合体のすべての末端は摩擦を小さくするために
アルキル基とくに炭素数1〜12のアルキル基によ
つてエーテル結合封鎖されたものである必要があ
る。ここで、末端が封鎖されていないと摩擦が大
きいという欠点があるので不適である。そして、
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ためであり、また
分子量1000未満の化合物(イ)は対金属など流体潤滑
的に好ましいが熱安定性に乏しく、また一方では
ゴム膨潤性が悪化するので好ましくない。分子量
が7000を越えると摩擦が大きくなるので不適であ
り、また一方では繊維―繊維間の静摩擦係数が極
端に低くなるため捲形状が不良となり、高速摩擦
仮撚の断糸の原因となり不利である。しかし、
7000以上のものを2〜3重量%以下併用すること
は差支えない。また、とくに分子量2000〜7000の
ものは油膜強化により糸表面を保護するとともに
前述した如くすべての末端封鎖化による平滑性も
良好で高速摩擦仮撚において毛羽防止に著しく効
果を示す。この際、末端封鎖の炭素数が12を越え
るようになるとヒーター汚れの原因となり易いの
で1〜12が望ましい。そして、化合物(イ)の油剤全
体に占める配合比は化合物(イ)の1種以上の合計量
として20〜99重量%が好ましい。
(ロ)は、上記(イ)のポリエーテル化合物のみではヒ
ーター汚れ防止が十分でなく、高速摩擦仮撚でヒ
ーター汚れ防止を格段に良くするために30℃にお
ける粘度が100センチポイズ以上の変性シリコン
を併用するものである。そして、その粘度が100
センチポイズ未満であるとヒーター上で飛散が大
きく、ヒーター汚れ防止の効果が十分でない。こ
の変性シリコンとは、ポリグリコール変性、高級
アルコール変性、脂肪酸変性、ポリオキシエチレ
ン変性、ポリエーテル変性等による変性シリコン
を挙げることができる。そして、化合物(ロ)の油剤
全体に占める配合比は0.2〜5重量%が好まし
い。
(ハ)は、ヒーター上のスカムの堆積を防止する効
果がある。こ炭素数1〜5のカルボン酸の塩とし
ては、たとえば炭素数1〜5のモノカルボン酸の
塩、一般式R―COOM(M=アルカリ金属、ア
ンモニウム、アミン)や炭素数1〜5のジカルボ
ン酸の塩、一般式MOOC―R―COOMを挙げる
ことができる。そして、化合物(ハ)の油剤全体に占
める配合比は0.1〜5重量%であることが好まし
い。
そして、本発明においてはこれら3成分の所定
の配合比(全体で100重量%)で配合した油剤組
成物は75℃の粘度が20〜60センチポイズで用いら
れる。
本発明にかかる油剤は、それを未延伸糸に0.2
〜0.7重量%程度付与することによつて、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、ニツト編地の緯段や織物布地の筋発
生のない均斉な加工糸が得られる。なお、本発明
の油剤に帯電防止のた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
塩を数%配合しても差支えない。
本発明の上述の油剤は、本発明以外の目的たと
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。
以下に実施例と比較例によつて本発明について
説明する。
実施例1〜5および比較例1〜4
常法によりポリエチレンテレフタレートを
3300m/分の紡糸速度で紡糸し、油剤組成物A〜
Iを別々に当該マルチフイラメントに対して油剤
付着量を0.5重量%目標に付与した(第1表)。得
られた120デニール/36フイラメント未延伸糸を
ウレタンゴム円板を備えた摩擦仮撚機を用いて延
伸倍率1.6倍、ヒーター温度220℃、摩擦円板回転
数8500rpm、加工速度700m/分で延伸しながら
摩擦仮撚を行なつた。各30日間づつ連続運転を行
ない、延伸仮撚性(毛羽、断糸、ヒータースカム
の発生、捲縮性)および得られた仮撚加工糸を編
物として染色仕上げして緯段発生状況を調査した
(第2表)。
これらの油剤のうちで実施例1〜5の油剤A〜
Eが種々検討したうちで代表的な本発明油剤であ
り、比較例1〜4の油剤F〜Iはなんらかの点で
劣つていた。以下にこれら実験例の結果について
考察する。
(1) 油剤A、B、C、D、Eは本発明油剤であつ
て、仮撚糸毛羽の発生および仮撚断糸の発生は
少なく、ヒーター汚れはほとんどなく、捲縮性
および編物の緯段もなく良好な結果が得られ
た。
(2) 油剤Fは全末端封鎖化したポリエーテルを主
体としたが、本発明の変性シリコンとカルボン
酸の塩を使用せずに一般的に知られているアル
キルスルホネートを使用した。その結果、仮撚
当初は毛羽、断糸なく緯段も観察されずに良好
であつたが、仮撚日数が増すにつれてヒーター
スカムやオイルドロツプが増し、捲縮性もバラ
ツキが多くなり、編地や織物に筋が発生した。
(3) 油剤Gは全末端封鎖化したポリエーテルを主
体とし、本発明の変性シリコンおよびカルボン
酸の塩を使用してはいるが、油剤の粘度が高く
なつたため平滑性不足による仮撚糸毛羽の発生
および仮撚断糸の発生が多くなり、また一方で
は捲縮不良と編地緯段が発生した。
(4) 油剤Hは末端封鎖化したポリエーテルではあ
るが、低分子量ポリエーテル(MW500)を多
量に配合した結果、ヒーター汚れが短時間で悪
化し、仮撚糸毛羽および仮撚断糸がヒーター汚
れとともに急激に増加した。仮撚当初、捲縮性
および編地の緯段は良好であつたが、ヒーター
汚れの悪化とともに捲縮性のバラツキが多くな
り、編地や織物に筋が発生した。
(5) 油剤Iは一般に知られているポリエーテル化
合物主体の配合油剤とした結果、平滑性不足に
よる仮撚糸毛羽の発生および仮撚断糸の発生が
多くなり、また一方では捲縮不良と編地緯段が
発生した。
The present invention mainly relates to a lubricant for high-speed drawing friction false twisting of polyester fibers, and more specifically, it is obtained as a uniform crimped yarn with hardly any heater stains observed during high-speed drawing friction false twisting.
The present invention relates to an oil agent for producing processed yarn, which can provide knitted fabrics and woven fabrics with excellent uniformity, and in particular to an oil agent for high-speed stretching and false twisting. Methods for obtaining processed polyester fiber yarns include a method in which undrawn yarn after spinning is temporarily turned into a drawn yarn and then false-twisted; and, with recent advances in DTY technology, drawing and false-twisting can be carried out simultaneously or continuously from a spun yarn. There are many ways to do this, and the latter is the most common. and,
The spindle false-twisting method and the friction false-twisting method have been adopted as methods for applying such stretch false-twisting, and in particular, by adopting the friction false-twisting method, the processing speed can be increased from 400 to 400.
Speeds are rapidly increasing to 1000m/min. However, as the processing speed increases, the friction between the yarn and various contacting bodies (for example, guides, rollers, heaters) increases, resulting in an increase in the occurrence of fuzz and yarn breakage due to damage to the fibers. On the other hand, due to the increase in the false twisting speed, the heater is significantly contaminated with conventionally well-known processing agents, and in extreme cases, tar and sludge residue (hereinafter abbreviated as scum) can be formed on the heater. The occurrence of fuzz and thread breakage increases. Furthermore, it causes the occurrence of abnormal crimping and dyeing spots, and the generation of streaks on the weft rows of knitted fabrics and woven fabrics.
Therefore, production must be stopped and the heaters must be cleaned frequently, resulting in poor operability. Recently, heat-resistant oils have been studied, and various oils based on polyether compounds have been proposed. When polyester multifilament yarns coated with a treatment agent containing polyether as a main component are subjected to high-speed friction false twisting, good results can be obtained against heater stains, but as the treatment time progresses, fluffing may occur. The occurrence of suture breakage is increasing. This causes crimp abnormalities and dyeing spots, and causes streaks in the weft rows of knitted fabrics and woven fabrics. In order to solve these problems, the present invention has been made through extensive research, and it has been discovered that it is possible to obtain a textured yarn with less heater stains, less fluff and yarn breakage, and a uniform crimpability without weft steps. It is something that That is, the present invention has a birefringence index (Δn) of 0.02 to
This invention relates to an oil agent for high-speed friction false-twisting that does not have the various disadvantages mentioned above when friction-false-twisting polyester undrawn multifilaments of about 0.08 in diameter at high processing speeds of several hundred to 1000 m/min. It is something. The origin of the present invention lies in an attempt to prevent the above-mentioned drawbacks of polyether compounds used as oil agents for high-speed friction false twisting. A remarkable effect was found by blending component (c). (b) PO/polyhydric alcohol added with block or random copolymer of ethylene oxide (EO) and propylene oxide (PO)
Comprised of one or more compounds with a molecular weight of 1000 to 7000 with an EO (molar ratio) of 40/60 to 90/10 and all terminals blocked by ether bonds with alkyl groups having 1 to 12 carbon atoms. 20 to 99% by weight (b) 0.2 to 5% by weight of modified silicone with a viscosity of 100 centipoise or more at 30°C (c) 0.1 to 5% by weight of a salt of a carboxylic acid having 1 to 5 carbon atoms. The roles of essential components (a) to (c) and the basis for selecting them will be explained. (A) improves the smoothness of the yarn, reduces fuzz and yarn breakage during high-speed friction false twisting, reduces crimp abnormalities, and provides processed yarn with fewer weft rows in knitted fabrics and fewer streaks in woven fabrics. It will be done. Also, there is very little dirt on the heater, which is good. The polyhydric alcohol of compound (a) in the present invention is a sorbitan-based or sorbitol-based polyhydric alcohol, pentaerythritol, trimethylolpropane, etc. Compound (a) is a polyhydric alcohol containing ethylene oxide (EO) and Propylene oxide (PO) is added, and the bonding state of the compound (a) may be block polymerization or random polymerization, but all the terminals of the copolymer are alkyl groups, especially carbon atoms 1 to reduce friction. The ether bond must be blocked by ~12 alkyl groups. Here, if the end is not sealed, it is unsuitable because it has the disadvantage of high friction. and,
The reason for setting the PO/EO (mole ratio) to 40/60 to 90/10 is to reduce heater contamination, and compounds (a) with a molecular weight of less than 1000 are preferable for fluid lubrication, such as with metals, but are thermally stable. It is not preferable because it has poor properties and, on the other hand, the rubber swelling property deteriorates. If the molecular weight exceeds 7000, friction will increase, making it unsuitable.On the other hand, the coefficient of static friction between fibers becomes extremely low, resulting in poor winding shape, which is disadvantageous as it causes yarn breakage during high-speed friction false twisting. . but,
7000 or more may be used in combination in an amount of 2 to 3% by weight or less. In addition, those having a molecular weight of 2,000 to 7,000 in particular protect the yarn surface by strengthening the oil film, and as mentioned above, have good smoothness due to all end-blocking, and are extremely effective in preventing fluffing during high-speed friction false twisting. At this time, if the number of carbon atoms in the terminal block exceeds 12, it is likely to cause contamination of the heater, so it is preferably 1 to 12 carbon atoms. The blending ratio of compound (a) in the entire oil agent is preferably 20 to 99% by weight as the total amount of one or more compounds (i). In (b), the polyether compound in (a) above is not sufficient to prevent heater stains, and in order to significantly improve heater stain prevention with high-speed friction false twisting, modified silicone with a viscosity of 100 centipoise or more at 30°C is used. They are used together. And its viscosity is 100
If it is less than centipoise, there will be a large amount of scattering on the heater, and the effect of preventing heater stains will not be sufficient. Examples of the modified silicone include silicone modified with polyglycol modification, higher alcohol modification, fatty acid modification, polyoxyethylene modification, polyether modification, and the like. The blending ratio of compound (b) to the entire oil agent is preferably 0.2 to 5% by weight. (C) has the effect of preventing the accumulation of scum on the heater. Examples of the salts of carboxylic acids having 1 to 5 carbon atoms include salts of monocarboxylic acids having 1 to 5 carbon atoms, general formula R-COOM (M=alkali metal, ammonium, amine), and dicarboxylic acids having 1 to 5 carbon atoms. Mention may be made of salts of acids with the general formula MOOC-R-COOM. The blending ratio of compound (c) to the entire oil agent is preferably 0.1 to 5% by weight. In the present invention, an oil composition containing these three components in a predetermined ratio (100% by weight in total) is used with a viscosity of 20 to 60 centipoise at 75°C. The oil agent according to the present invention is applied to undrawn yarn by 0.2
By adding approximately 0.7% by weight, high-speed friction false twisting results in less fuzz and yarn breakage, no crimp abnormalities, and uniform knitted fabrics with no weft rows or streaks on woven fabrics. Processed yarn is obtained. It should be noted that several percent of alkyl sulfonate salts and alkyl phosphate salts, which are generally known for antistatic purposes, may be blended into the oil agent of the present invention. The above-mentioned oil agent of the present invention can be used for purposes other than the present invention, for example, as a treatment agent for spindle-type false-twisting yarn, a yarn treatment agent for spinning and drawing synthetic fibers, and still have some effects. The present invention will be explained below using Examples and Comparative Examples. Examples 1 to 5 and Comparative Examples 1 to 4 Polyethylene terephthalate was prepared by a conventional method.
Spinning at a spinning speed of 3300 m/min, oil composition A~
I was separately applied to the multifilament with an oil adhesion target of 0.5% by weight (Table 1). The obtained 120 denier/36 filament undrawn yarn was stretched using a friction false twisting machine equipped with a urethane rubber disc at a stretching ratio of 1.6 times, a heater temperature of 220°C, a friction disc rotation speed of 8500 rpm, and a processing speed of 700 m/min. At the same time, frictional false twisting was performed. Continuous operation was carried out for 30 days each, and the drawing false twist properties (fuzz, yarn breakage, occurrence of heater scum, crimp properties) and the resulting false twisted yarns were dyed and finished as knitted fabrics to investigate the occurrence of weft steps. (Table 2). Among these oils, oils A to Examples 1 to 5
E is a representative oil agent of the present invention among various studies, and oil agents F to I of Comparative Examples 1 to 4 were inferior in some respects. The results of these experimental examples will be discussed below. (1) Oils A, B, C, D, and E are the oils of the present invention, which cause less occurrence of false twist yarn fluff and false twist breakage, almost no heater stain, and improved crimpability and weft row of knitted fabrics. Good results were obtained. (2) Oil agent F was mainly composed of polyether with all ends capped, but instead of using the modified silicone and carboxylic acid salt of the present invention, a commonly known alkyl sulfonate was used. The results showed that the results were good at the beginning of false twisting, with no fuzz, no yarn breakage, and no weft steps observed. However, as the number of days of false twisting increased, heater scum and oil drops increased, and crimpability also increased, resulting in poor knitted fabrics. Streaks appeared in the fabric. (3) Oil agent G is mainly made of polyether with all ends blocked, and uses the modified silicone and carboxylic acid salt of the present invention, but due to the increased viscosity of the oil agent, the false-twisted yarn is fluffy due to lack of smoothness. The number of occurrences of breakage and false-twisted yarns increased, and on the other hand, poor crimp and weft rows of knitted fabrics occurred. (4) Oil agent H is an end-capped polyether, but as a result of blending a large amount of low molecular weight polyether (MW500), heater stains worsen in a short period of time, and the false-twisted yarn fuzz and false-twisted broken yarn become heater stains. It increased rapidly. At the beginning of false twisting, the crimpability and the weft row of the knitted fabric were good, but as the heater stain worsened, the crimpability became more uneven, and streaks appeared in the knitted fabric or woven fabric. (5) As a result of using Oil I as a compounded oil mainly composed of a generally known polyether compound, the occurrence of false twist yarn fuzz and false twist breakage due to lack of smoothness increased, and on the other hand, it caused poor crimping and knitting. A geolatitudinal step occurred.
【表】【table】
Claims (1)
75℃における粘度が20〜60センチポイズであるこ
とを特徴とする摩擦仮撚用油剤。 (イ) 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)のブロ
ツクまたはランダム共重合物を付加したPO/
EO(モル比)が40/60〜90/10にして、すべ
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た分子量1000〜7000の化
合物1種以上で構成されたものを20〜99重量% (ロ) 30℃における粘度が100センチポイズ以上の
変性シリコンを0.2〜5重量% (ハ) 炭素数1〜5のカルボン酸の塩を0.1〜5重
量%[Scope of Claims] 1 Consists of a mixed composition of the following compounds (a) to (c),
An oil for friction false twisting characterized by a viscosity of 20 to 60 centipoise at 75°C. (b) PO/polyhydric alcohol added with block or random copolymer of ethylene oxide (EO) and propylene oxide (PO)
Comprised of one or more compounds with a molecular weight of 1000 to 7000 with an EO (molar ratio) of 40/60 to 90/10 and all terminals blocked by ether bonds with alkyl groups having 1 to 12 carbon atoms. 20 to 99% by weight of (b) 0.2 to 5% by weight of modified silicone with a viscosity of 100 centipoise or more at 30°C (c) 0.1 to 5% by weight of a salt of a carboxylic acid having 1 to 5 carbon atoms
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18392783A JPS6075676A (en) | 1983-09-30 | 1983-09-30 | Oil agent for friction false twisting |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP18392783A JPS6075676A (en) | 1983-09-30 | 1983-09-30 | Oil agent for friction false twisting |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6075676A JPS6075676A (en) | 1985-04-30 |
JPS6254910B2 true JPS6254910B2 (en) | 1987-11-17 |
Family
ID=16144240
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP18392783A Granted JPS6075676A (en) | 1983-09-30 | 1983-09-30 | Oil agent for friction false twisting |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6075676A (en) |
-
1983
- 1983-09-30 JP JP18392783A patent/JPS6075676A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS6075676A (en) | 1985-04-30 |
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