JPH0457965A - Spinning oil for synthetic fiber - Google Patents

Spinning oil for synthetic fiber

Info

Publication number
JPH0457965A
JPH0457965A JP2171053A JP17105390A JPH0457965A JP H0457965 A JPH0457965 A JP H0457965A JP 2171053 A JP2171053 A JP 2171053A JP 17105390 A JP17105390 A JP 17105390A JP H0457965 A JPH0457965 A JP H0457965A
Authority
JP
Japan
Prior art keywords
weight
spinning
fatty acid
phosphate ester
synthetic fibers
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.)
Granted
Application number
JP2171053A
Other languages
Japanese (ja)
Other versions
JP2948874B2 (en
Inventor
Hidehiko Arai
英彦 荒井
Hiroshi Ogawara
浩 大河原
Masafumi Moriya
雅文 守屋
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Miyoshi Yushi KK
Miyoshi Oil and Fat Co Ltd
Original Assignee
Miyoshi Yushi KK
Miyoshi Oil and Fat Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Miyoshi Yushi KK, Miyoshi Oil and Fat Co Ltd filed Critical Miyoshi Yushi KK
Priority to JP2171053A priority Critical patent/JP2948874B2/en
Publication of JPH0457965A publication Critical patent/JPH0457965A/en
Application granted granted Critical
Publication of JP2948874B2 publication Critical patent/JP2948874B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Abstract

PURPOSE:To provide a synthetic fiber-spinning oil containing an alkyl phosphate ester, an aliphatic acid amide having a specific amine value, a nonionic surfactant and, if necessary, a lower alkanolamine salt in a specific ratio and giving good spinnability and excellent product touch to the synthetic fibers. CONSTITUTION:An oil for spinning synthetic fibers contains (A) 5-80wt.% of an alkyl phosphate ester, (B) 5-80wt.% of a higher fatty acid amide obtained from a polyalkylenepolyamine or alkanolamine and a 10-26C saturated fatty acid and having an all amine value of <=30, (C) 5-80wt.% of a nonionic surfactant and, if necessary, (D) 3-20wt.% of the quaternary ammonium salt of a lower alkanolamine. The component A includes compounds of formulas I and II (R is 4-18C alkyl, 4-18C alkenyl; A is oxyethylene, oxypropylene; (n) is 0-10; (l), (m)are 0-3; X is alkali metal, organic amine).

Description

【発明の詳細な説明】 [産業上の利用分野コ 本発明は合成繊維用紡績油剤に間する。さらに詳しくは
、合成繊維の紡糸工程あるいは紡績工程に用いて良好な
紡糸性、紡績性を発揮し、かつ染色後の繊維製品に優れ
た風合を付与せしめることのできる合成繊維用紡績油剤
に間するものである。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a spinning oil for synthetic fibers. More specifically, it is a spinning oil agent for synthetic fibers that can be used in the spinning or spinning process of synthetic fibers to exhibit good spinnability and spinnability, as well as to impart excellent texture to textile products after dyeing. It is something to do.

[従来の技術] 一般に合成繊維の紡績を良好に行うためには、合成繊維
に帯電防止性、集束性、平滑性、防錆性等の種々の性能
を付与する必要がある。
[Prior Art] Generally, in order to spin synthetic fibers well, it is necessary to impart various properties to the synthetic fibers, such as antistatic properties, cohesion properties, smoothness, and rust prevention properties.

これらの性能を向上させるために、各性能を付与せしめ
る成分を組み合わせた種々の紡績油剤が用いられている
In order to improve these performances, various spinning oils are used that combine components that provide each performance.

例えば帯電防止性を付与する成分としては、アルキルリ
ン酸エステル塩、アルキル硫酸エステル塩、第四級アン
モニウム化合物、ベタイン化合物等が用いられ、集束性
を付与する成分としては、ポリオキシアルキレンフェニ
ルエーテル、ポリオキシアルキレンアルキルエーテル、
ポリオキシアルキレンアルキルエステル等が用いられて
いる。
For example, as a component that imparts antistatic properties, alkyl phosphate salts, alkyl sulfate salts, quaternary ammonium compounds, betaine compounds, etc. are used, and as components that impart focusing properties, polyoxyalkylene phenyl ether, polyoxyalkylene alkyl ether,
Polyoxyalkylene alkyl esters and the like are used.

また平滑性を付与する成分としては、アルキルアルキレ
ート、多価アルコールエステル、ポリアルキレンゲリコ
ールアルキルエステル、パラフィン、α−オレフィン等
が用いられている。
In addition, as components for imparting smoothness, alkyl alkylates, polyhydric alcohol esters, polyalkylene gelicol alkyl esters, paraffins, α-olefins, and the like are used.

[従来技術の問題点] しかしながら、従来から知られているこれらの紡績油剤
は応用範囲の狭いものであった。
[Problems with the Prior Art] However, these conventionally known spinning oils have a narrow range of application.

例えば紡績工程の後で行う編立工程では、繊維に平滑性
、柔軟性等の性能を付与する必要があり、紡績工程とは
異なった性能が要求される。従来の紡績油剤は紡績工程
に用いられて良好な紡績性能を発揮しても、膳立工程迄
効果の持続するものが少なく、又持続しても同工程で要
求される性能を満たすことができない。その為編立工程
では別途に膳立油剤を用いる必要がある。
For example, in the knitting process performed after the spinning process, it is necessary to impart properties such as smoothness and flexibility to the fibers, and different performance is required from that in the spinning process. Even if conventional spinning oils are used in the spinning process and exhibit good spinning performance, their effects rarely last until the setting process, and even if they last, they cannot meet the performance required in the same process. . Therefore, it is necessary to use a separate cooking oil in the knitting process.

一方、繊維製品は天然繊維製品の持つ風合が好まれ、合
成繊維製品にも天然繊維製品の同様の柔軟性、平滑性に
富んだ風合が望まれるが、従来の紡績油剤では、この様
な風合を付与することができず、さらに柔軟剤、平滑剤
等の仕上剤を用いる必要がある。
On the other hand, textile products are preferred to have the feel of natural fiber products, and synthetic fiber products are also desired to have the same softness and smoothness as natural fiber products, but conventional spinning oils do not have the same softness and smoothness as natural fiber products. It is not possible to impart a unique texture to the product, and it is necessary to use finishing agents such as softeners and smoothing agents.

この様に、従来の紡績油剤は、紡績工程でのみ性能を発
揮するもので適用範囲が狭く、合成繊維製品を製造する
為には、他に種々の油剤を必要とし、経済性の劣るもの
であった。
In this way, conventional spinning oils exhibit their performance only in the spinning process and have a narrow scope of application.In order to manufacture synthetic fiber products, various other oils are required, making them less economical. there were.

本発明は上記問題点に着目し行ったもので、紡糸あるい
は紡績工程で用いると、編立工程を経て染色後の製品に
至るまでの各工程で必要とされる性能を満足し、良好な
風合を有する合成繊維製品を製造することのできる、合
成繊維用紡績油剤を提供することを目的とする。
The present invention was developed by focusing on the above problems, and when used in the spinning or spinning process, it satisfies the performance required in each process from the knitting process to the dyed product, and has good wind resistance. It is an object of the present invention to provide a spinning oil agent for synthetic fibers, which can produce synthetic fiber products having the same properties as the synthetic fibers.

[問題点を解決するための手段] 本発明者らは上記!!!題を解決するために鋭意研究を
行った結果、アルキルリン酸エステル塩、高級脂肪酸ア
ミド化合物、非イオン界面活性剤もしくはこれに低級ア
ルカノールアミンの四級アンモニウム塩を特定比で含有
してなる組成物が、合成繊維の紡績工程に用いて、紡績
工程からその後の各工程で必要とされる各性能を発揮し
、さらに良好な風合を有する合成!!維製品を製造する
ことのできる油剤であることを見出し本発明に至った。
[Means for solving the problem] The inventors have solved the problem above! ! ! As a result of extensive research to solve this problem, we have discovered a composition containing an alkyl phosphate ester salt, a higher fatty acid amide compound, a nonionic surfactant, or a quaternary ammonium salt of a lower alkanolamine in a specific ratio. However, when used in the spinning process of synthetic fibers, it exhibits the performance required from the spinning process to each subsequent process, and also has a good texture! ! The present invention was based on the discovery that it is an oil agent that can be used to manufacture textile products.

即ち、本発明の要旨の一つは、(A)アルキルリン酸エ
ステル塩6〜80重量%、(B)全アミン価が30以下
の高級脂肪酸アミド化合物5〜80重量%、(C)非イ
オン界面活性剤5〜80重量%を含有する合成繊維用紡
績油剤である。
That is, one of the gist of the present invention is that (A) 6-80% by weight of an alkyl phosphate ester salt, (B) 5-80% by weight of a higher fatty acid amide compound having a total amine value of 30 or less, (C) nonionic This is a spinning oil for synthetic fibers containing 5 to 80% by weight of a surfactant.

また本発明のいま一つの要旨は(A)アルキルリン酸エ
ステル塩5〜80重量%、(B)全アミン価が30以下
の高級脂肪酸アミド化合物5〜80重量%、(C)非イ
オン界面活性剤5〜80重量%、(D)低級アルカノー
ルアミンの四級アンモニウム塩3〜20重量%を含有す
る合成繊維用紡績油剤である。
Another gist of the present invention is (A) 5-80% by weight of an alkyl phosphate ester salt, (B) 5-80% by weight of a higher fatty acid amide compound having a total amine value of 30 or less, (C) nonionic surface activity. This is a spinning oil agent for synthetic fibers containing 5 to 80% by weight of the agent and 3 to 20% by weight of (D) the quaternary ammonium salt of lower alkanolamine.

本発明に用いる(A)のアルキルリン酸エステル塩は、
下記一般式(1)及び又は(2)RO−(A) n−P
−0−(A) I、X・・(1)0− (A) mX で示されるアルキルリン酸エステル塩が挙げられる。(
1)式及び(2)式中、Rは炭素数4〜18のアルキル
基又はアルケニル基が好ましく、又Aはオキシエチレン
基及び又はオキシプロピレン基、nは0〜10.1及び
mはO〜3、Xはアルカリ金属又は有機アミンが好まし
い。
The alkyl phosphate ester salt (A) used in the present invention is:
The following general formula (1) and or (2) RO-(A) n-P
Examples include alkyl phosphate ester salts represented by -0-(A)I,X...(1)0-(A)mX. (
In formulas 1) and (2), R is preferably an alkyl group or alkenyl group having 4 to 18 carbon atoms, A is an oxyethylene group and/or an oxypropylene group, n is 0 to 10.1, and m is O to 3. X is preferably an alkali metal or an organic amine.

上記アルキルリン酸エステル塩は、炭素数4〜18の脂
肪族アルコール、該脂肪族アルコールにエチレンオキサ
イド又はプロピレンオキサイドを1〜10モル付加した
付加化合物を、常法に従いリン酸エステル化し、次いて
必要に応じエチしンオキサイド又はプロピレンオキサイ
ドを3モル以下反応させた後、アルカリ金属の水酸化物
、又は有機アミン化合物で中和して得られる。
The above alkyl phosphate ester salt is obtained by phosphoric acid esterification of an aliphatic alcohol having 4 to 18 carbon atoms, an addition compound obtained by adding 1 to 10 moles of ethylene oxide or propylene oxide to the aliphatic alcohol, according to a conventional method, and then It is obtained by reacting 3 moles or less of ethyne oxide or propylene oxide depending on the situation, and then neutralizing it with an alkali metal hydroxide or an organic amine compound.

ここに用いる脂肪族アルコールとしては、ブチルアルコ
ール、オクチルアルコール、ラウリルアアルコール、七
チルアルコール、ステアリルアルコール、オレイルアル
コール、イソブチルアルコール、イソオクチルアルコー
ル、イソステアリルアルコール等の炭素数4〜18の脂
肪族アルコール、及びα−オレフィン、n−オレフィン
、n−パラフィンなどを原料にして得られる合成高級ア
ルコールが挙げられ、リン酸エステル化反応に用いられ
るリン化合物としては五酸化リンが挙げられる。リン酸
エステル化反応において、モノアルキルリン酸エステル
、ジアルキルリン酸エステル及びこれらの混合物が得ら
れ、これらはいずれも用いることができる。アルカリ金
属の水酸化物としては、水酸化ナトリウム、水酸化カリ
ウム等が挙げられ、有機アミン化合物としてはアンモニ
ア、モノエタノールアミン、ジェタノールアミン、トリ
エタノールアミン等が挙げられる。
The aliphatic alcohol used here includes aliphatic alcohols having 4 to 18 carbon atoms such as butyl alcohol, octyl alcohol, lauryl alcohol, heptyl alcohol, stearyl alcohol, oleyl alcohol, isobutyl alcohol, isooctyl alcohol, isostearyl alcohol, etc. , and synthetic higher alcohols obtained using α-olefins, n-olefins, n-paraffins, etc. as raw materials, and phosphorus compounds used in the phosphoric acid esterification reaction include phosphorus pentoxide. In the phosphoric acid esterification reaction, monoalkyl phosphates, dialkyl phosphates, and mixtures thereof are obtained, and any of these can be used. Examples of alkali metal hydroxides include sodium hydroxide and potassium hydroxide, and examples of organic amine compounds include ammonia, monoethanolamine, jetanolamine, triethanolamine, and the like.

本発明の合成繊維用紡績油剤における上記アルキルリン
酸エステル塩の含量は5〜80重量%が好ましく、5〜
40重量%がより好ましい。アルキルリン酸エステル塩
の含量が5重量%未満であると、帯電防止性、防錆性が
不足し、紡績時に繊維がフロントローラーに巻き付く、
あるいはローラニが錆びる等の現象を防ぐことができな
い。又80重量%を越えると帯電防止性、防錆性は良く
なるが、繊維−金属間の平滑性が低下し、また得られる
縦!!!!品の風合が低下する。
The content of the alkyl phosphate ester salt in the spinning oil for synthetic fibers of the present invention is preferably 5 to 80% by weight, and 5 to 80% by weight.
40% by weight is more preferred. If the content of the alkyl phosphate ester salt is less than 5% by weight, antistatic properties and rust prevention properties will be insufficient, and fibers may wind around the front roller during spinning.
Or, it is not possible to prevent phenomena such as rusting of the rollers. If it exceeds 80% by weight, the antistatic properties and rust prevention properties will improve, but the smoothness between the fiber and the metal will decrease, and the resulting warp! ! ! ! The texture of the product deteriorates.

本発明に用いる(B)の高級脂肪酸アミド化合物には、
ポリアルキレンポリアミン又はアルカノールアミンと炭
素数10〜26の飽和脂肪酸とを用い、常法に従いアミ
F化反応を行って得られ、全アミン価が30以下の高級
脂肪酸アミド化合物、及び全アミン価が30以上の化合
物にあっては、それに尿素、エビへロヒドリン等を反応
せしめ全アミン価を30以下にした高級脂肪酸アミド化
合物が挙げられる。またこれらのアミド化合物のうち、
アミン価を有するものは酸で中和して用いることもてき
る。上記ポリアルキレンポリアミンとしては、エチレン
ジアミン、ジエチレントリアミン、トリエチレンテトラ
ミン、テトラエチレンペンタミン、ペンタエチレンへキ
サミン等が挙げられ、アルカノールアミンとしては、モ
ノエタノールアミン、ジェタノールアミン、トリエタノ
ールアミン、N−(2−アミノエチル)−エタノールア
ミン等が挙げられる。また炭素数10〜26の飽和脂肪
酸としては、ラウリン酸、ミリスチン酸、バルミチン酸
、ステアリン酸、アラキン酸、ベヘン酸等が挙げられ、
これらの高級脂肪酸は単独でも、また2種以上混合した
ものであっても良い。
The higher fatty acid amide compound (B) used in the present invention includes:
A higher fatty acid amide compound having a total amine value of 30 or less and a higher fatty acid amide compound having a total amine value of 30 or less, which is obtained by carrying out an amine-F reaction using a polyalkylene polyamine or an alkanolamine and a saturated fatty acid having 10 to 26 carbon atoms according to a conventional method. Examples of the above-mentioned compounds include higher fatty acid amide compounds which have a total amine value of 30 or less by reacting them with urea, shrimp herohydrin, etc. Also, among these amide compounds,
Those having an amine value can also be used after being neutralized with an acid. Examples of the polyalkylene polyamines include ethylenediamine, diethylenetriamine, triethylenetetramine, tetraethylenepentamine, pentaethylenehexamine, etc., and examples of the alkanolamines include monoethanolamine, jetanolamine, triethanolamine, N-(2 -aminoethyl)-ethanolamine, and the like. Examples of saturated fatty acids having 10 to 26 carbon atoms include lauric acid, myristic acid, valmitic acid, stearic acid, arachidic acid, and behenic acid.
These higher fatty acids may be used alone or in combination of two or more.

2種以上混合した高級脂肪酸としては、動植物油脂、あ
るいはこれらの動植物油脂を水素添加した水添硬化油脂
等の油脂類を、常法に従って高圧分解あるいは油脂分解
酵素を用いて分解して得られる脂肪酸が挙げられる。上
記高級脂肪酸アミド化合物は、全アミン価30以下のも
のがアルキルリン酸エステル塩との相溶性に優れ、繊維
製品に良好な風合を付与することができる。全アミン価
が30を越えるものはアルキルリン酸エステル塩との相
溶性が低く好ましくなく、安定な製品及び水溶液が得ら
れ難い。
The higher fatty acids that are a mixture of two or more types include fatty acids obtained by decomposing animal and vegetable oils or fats such as hydrogenated hydrogenated oils and fats obtained by hydrogenating these animal and vegetable oils using conventional methods such as high-pressure decomposition or using fat-degrading enzymes. can be mentioned. The above-mentioned higher fatty acid amide compound having a total amine value of 30 or less has excellent compatibility with the alkyl phosphate ester salt and can impart a good feel to textile products. Those having a total amine value of more than 30 are undesirable because of their low compatibility with alkyl phosphate ester salts, and it is difficult to obtain stable products and aqueous solutions.

本発明の合成繊維紡績油剤における上記高級脂肪酸アミ
ド化合物の含量は、5〜80重量%が好ましく、5〜4
0重量%がより好ましい。高級脂肪酸アミド化合物の含
量が5重量%未満では、繊維製品に風合を付与する効果
が少なく、また80重量%を越えると繊維の帯電を防止
することが難しく、さらに繊維間の集束性も十分でなく
抱合力が不足し好ましくない。
The content of the higher fatty acid amide compound in the synthetic fiber spinning oil of the present invention is preferably 5 to 80% by weight, and 5 to 4% by weight.
0% by weight is more preferred. If the content of the higher fatty acid amide compound is less than 5% by weight, it will have little effect in imparting texture to textile products, and if it exceeds 80% by weight, it will be difficult to prevent the fibers from being electrostatically charged, and the cohesiveness between the fibers will also be insufficient. However, the conjugation power is insufficient, which is undesirable.

本発明に用いる(C)の非イオン界面活性剤としては、
ポリオキシエチレンアルキルエーテル、ポリオキシエチ
レンアルキルフェニルエーテル、ポリオキシエチレンス
チリルエーテル、ポリオキシエチレンヒマシ油エーテル
、ポリオキシエチレン・ポリオキシブCピレンブロック
共重合体等のエーテル型非イオン界面活性剤、ソルビタ
ン脂肪酸部分エステル、グリセリン脂肪酸部分エステル
、ポリグリセリン(重合度2〜10)脂肪酸部分エステ
ル、ペンタエリスリトール脂肪酸部分エステル、ポリエ
チレングリコール脂肪酸モノエステルあるいはジエステ
ル、ポリプロピレングリコール脂肪酸モノエステルある
いはジエステル、ショ糖脂肪酸部分エステル等の脂肪酸
エステル型非イオン界面活性剤、及びこれらのうちの部
分エステルにエチレンオキサイドを付加した非イオン界
面活性剤が挙げられる。ポリオキシエチレン・ポリオキ
シプロピレンブロック共重合体を除くエーテル型非イオ
ン界面活性剤のポリオキシエチレン基はエチレンオキサ
イドを付加して得られ、その付加モル数は5〜50モル
が好ましく、またアルキル基の鎖長は炭素数12〜18
が好ましい。ポリオキシエチレン・ポリオキシプロピレ
ンブロック共重合体は、分子量が500〜20000が
好ましく、同範囲の分子量を有するものはエチレンオキ
サイドとプロピレンオキサイドの付加モル数の比及び付
加順序がいずれであっても用いることができる。またエ
ステル型非イオン界面活性剤の脂肪酸基は炭素数12〜
18が好ましく、部分エステルに付加するエチレンオキ
サイドの付加モル数は3〜20モルが好ましい。
As the nonionic surfactant (C) used in the present invention,
Ether type nonionic surfactants such as polyoxyethylene alkyl ether, polyoxyethylene alkyl phenyl ether, polyoxyethylene styryl ether, polyoxyethylene castor oil ether, polyoxyethylene/polyoxybuC pyrene block copolymer, sorbitan fatty acid moiety Fatty acids such as esters, glycerin fatty acid partial esters, polyglycerin (degree of polymerization 2 to 10) fatty acid partial esters, pentaerythritol fatty acid partial esters, polyethylene glycol fatty acid monoesters or diesters, polypropylene glycol fatty acid monoesters or diesters, sucrose fatty acid partial esters, etc. Examples include ester type nonionic surfactants and nonionic surfactants obtained by adding ethylene oxide to partial esters of these. The polyoxyethylene group of the ether type nonionic surfactant other than the polyoxyethylene/polyoxypropylene block copolymer is obtained by adding ethylene oxide, and the number of moles added is preferably 5 to 50 moles, and the number of moles added is preferably 5 to 50 moles. chain length is 12 to 18 carbon atoms
is preferred. The polyoxyethylene/polyoxypropylene block copolymer preferably has a molecular weight of 500 to 20,000, and those having a molecular weight in the same range are used regardless of the molar ratio of ethylene oxide and propylene oxide added and the order of addition. be able to. In addition, the fatty acid group of the ester type nonionic surfactant has 12 or more carbon atoms.
The number of moles of ethylene oxide added to the partial ester is preferably 3 to 20 moles.

本発明の合成繊維用紡績油剤における上記非イオン界面
活性剤の含量は5〜80重量%が好ましく、5〜40重
量%がより好ましい。その含量が5重量%未満では油剤
としての乳化力が弱く、水に乳化して用いることが難し
く、また80重量%を越えると高級脂肪酸アミド化合物
による繊維製品へ風合を付与する効果が低下し、帯電防
止性も低下する。
The content of the nonionic surfactant in the spinning oil for synthetic fibers of the present invention is preferably 5 to 80% by weight, more preferably 5 to 40% by weight. If the content is less than 5% by weight, the emulsifying power as an oil agent is weak and it is difficult to use it by emulsifying it in water, and if it exceeds 80% by weight, the effect of the higher fatty acid amide compound in imparting texture to textile products decreases. , the antistatic property also decreases.

本発明の合成繊維用紡績油剤は、上記(A)アルキルリ
ン酸エステル塩、(、B)高級脂肪酸アミド化合物及び
(C)非イオン界面活性剤を所定量含有することにより
、良好な紡績性を発揮し、繊維製品に優れた風合を付与
することができるが、これに(D)低級アルカノールア
ミンの四級アンモニウム塩を含有せしめると、これらの
性能を向上させると共に、特に(A)のアルキルリン酸
エステル塩と相剰的に作用して、帯電防止性をさらに高
めることができる。
The spinning oil for synthetic fibers of the present invention has good spinning properties by containing the above (A) alkyl phosphate ester salt, (B) higher fatty acid amide compound, and (C) nonionic surfactant in predetermined amounts. However, when it contains (D) a quaternary ammonium salt of lower alkanolamine, these properties can be improved, and especially the alkyl of (A) can be improved. The antistatic property can be further enhanced by acting additively with the phosphate ester salt.

本発明に用いる(D)低級アルカノールアミンの四級ア
ンモニウム塩としては、モノエタノールアミン、ジェタ
ノールアミン、トリエタノールアミン、N−(2−アミ
ノエチル)−エタノールアミン等の低級アルカノールア
ミンをジメチル硫酸、ジエチル硫酸で四級化して得られ
る四級アンモニウム塩が挙げられる。
As the quaternary ammonium salt of lower alkanolamine (D) used in the present invention, lower alkanolamines such as monoethanolamine, jetanolamine, triethanolamine, N-(2-aminoethyl)-ethanolamine, dimethyl sulfate, Examples include quaternary ammonium salts obtained by quaternization with diethyl sulfate.

上記四級アンモニウム塩の含量は20重量%以下が好ま
しく、3〜20重量%がより好ましい。
The content of the quaternary ammonium salt is preferably 20% by weight or less, more preferably 3 to 20% by weight.

その含量が20重量%を越えると、帯電防止性が高くな
るものの防錆性が低下する。
When the content exceeds 20% by weight, the antistatic property becomes high but the rust preventive property decreases.

本発明の合成am用紡績油剤は、前記(A)アルキルリ
ン酸エステル塩、(B)高級脂肪酸アミド化合物、(C
)非イオン界面活性剤、(D)低級アルカノールアミン
の四級アンモニウム塩を主成分とするが、これに必要に
応じて高級脂肪酸アルコールエステル、動植物油脂、鉱
物油;ワックス類、シリコン系化合物等の、従来知られ
ている柔軟剤、平滑剤を配合することもできる。その配
合量は20重量%以下が好ましい。
The synthetic AM spinning oil of the present invention comprises the above-mentioned (A) alkyl phosphate ester salt, (B) a higher fatty acid amide compound, (C
) Nonionic surfactant, (D) Quaternary ammonium salt of lower alkanolamine as the main component, but if necessary, higher fatty acid alcohol ester, animal or vegetable oil, mineral oil; waxes, silicone compounds, etc. , conventionally known softeners and smoothing agents can also be blended. The blending amount is preferably 20% by weight or less.

本発明の合成繊維用紡績油剤は、前記各成分を所定量混
合し、均一に溶解して調製することができる。
The spinning oil for synthetic fibers of the present invention can be prepared by mixing predetermined amounts of each of the above components and uniformly dissolving the mixture.

本発明の合成繊維用紡績油剤は合成繊維の紡績工程にお
いて用いられ、合成繊維の原糸を該油剤で処理した後紡
績を行う方法、紡績中の繊維に給油処理する方法等、い
ずれの方法も採用できる。
The spinning oil agent for synthetic fibers of the present invention is used in the spinning process of synthetic fibers, and can be used in any of the following methods, including a method in which the raw yarn of synthetic fibers is treated with the oil agent and then spun, a method in which the fibers are oiled during spinning, etc. Can be adopted.

原糸を処理する方法としては、浸漬給油法、ローラータ
ッチ給油法、スプレー給油法等が挙げられる。また給油
に際し、油剤を水で希釈して0.01〜2重量%程度の
濃度にて用いることが好ましい。
Examples of methods for treating the raw yarn include a dipping oiling method, a roller touch oiling method, a spray oiling method, and the like. Further, when refueling, it is preferable to dilute the oil agent with water and use it at a concentration of about 0.01 to 2% by weight.

本発明の合成繊維用紡績油剤はポリアクリロニトリル繊
維、ポリアミド繊維、ポリエステル繊維、ポリプロピレ
ン繊維等の合成繊維に適用でき、特にポリアクリロニト
リル繊維、ポリアミド繊維に用いて良好な紡績性を発揮
する。
The spinning oil agent for synthetic fibers of the present invention can be applied to synthetic fibers such as polyacrylonitrile fibers, polyamide fibers, polyester fibers, and polypropylene fibers, and exhibits good spinnability especially when used with polyacrylonitrile fibers and polyamide fibers.

以下、実施例により本発明をさらに詳細に説明するが、
本発明はその要旨を越えない限り、以下の実施例に限定
されるものではない。
Hereinafter, the present invention will be explained in more detail with reference to Examples.
The present invention is not limited to the following examples unless it exceeds the gist thereof.

[実施例] 実施例、参考例及び比較例に用いた各化合物を次に示す
。()内は略号を表す。
[Example] Compounds used in Examples, Reference Examples, and Comparative Examples are shown below. The numbers in parentheses represent abbreviations.

A・アルキルリン酸エステル塩 (A−1)ヒドロキシエチルオクチルアルコールエーテ
ルリン酸エステルモノエタノールアミン塩(A−2)オ
クチルアルコールリン酸エステルカリウム塩 (A−3)ラウリルアルコールリン酸エステルジェタノ
ールアミン塩 (A−4)ポリオキシエチレン(n=7)ラウリルアル
コールエーテルリン酸エステルナトリウム塩(A−5)
オクチルアルコールリン酸エステルモノエタノールアミ
ン塩 (A−6)セチルアルコールリン酸エステルカリウム塩 B・高級脂肪酸アミド化合物 高級脂肪酸アミド化合物は以下に示す様に合成したもの
を用いた。
A. Alkyl phosphate ester salt (A-1) Hydroxyethyl octyl alcohol ether phosphate ester monoethanolamine salt (A-2) Octyl alcohol phosphate ester potassium salt (A-3) Lauryl alcohol phosphate ester jetanolamine salt (A-4) Polyoxyethylene (n=7) lauryl alcohol ether phosphate ester sodium salt (A-5)
Octyl alcohol phosphate ester monoethanolamine salt (A-6) Cetyl alcohol phosphate ester potassium salt B/Higher fatty acid amide compound The higher fatty acid amide compound was synthesized as shown below.

撹拌機付の反応容器に、表1に示す高級脂肪酸及びポリ
アルキレンポリアミン又はアルカノールアミンを所定の
比で仕込み、窒素ガス気流下に170〜200℃で6時
間脱水反応を行い、高級脂肪酸アミド化合物(B−1,
3,7)を得た。さらに同様なアミド反応を行った後、
所定量の尿素、エピクロルヒドリンを加え、90〜13
0℃で1〜2時間反応を行い、高級脂肪酸アミド化合物
B−2,4〜6を得た。各化合物の合成条件、全アミン
価及び略号を表1に示す。
A reaction vessel equipped with a stirrer was charged with higher fatty acids and polyalkylene polyamines or alkanolamines shown in Table 1 in a predetermined ratio, and a dehydration reaction was carried out at 170 to 200°C for 6 hours under a nitrogen gas flow to obtain a higher fatty acid amide compound ( B-1,
3,7) were obtained. After further performing a similar amide reaction,
Add predetermined amounts of urea and epichlorohydrin to 90-13
The reaction was carried out at 0°C for 1 to 2 hours to obtain higher fatty acid amide compounds B-2, 4 to 6. Table 1 shows the synthesis conditions, total amine value, and abbreviations of each compound.

C・非イオン界面活性剤 (C−1)ポリオキシエチレン(n=7)ラウリルエー
テル (C−2)ポリオキシエチレン(n=25)セチルエー
テル 表1 本:酢酸塩 (C−3)ポリオキシエチレン(n=25)ヒマシ油エ
ーテル (C−4)ポリオキシエチレン(n=20)ノニルフェ
ニルエーテル (C−5)ポリオキシエチレン(n=20)ソルビタン
モノラウリルエステル (C−6)ポリエチレングライコール(MW400)ジ
ラウレート D・低級アルカノールアミンの四級アンモニウム塩(D
−1)N−(2−アミノエチル)エタノールジエチル硫
酸塩 (D−2)モノエタノールアミンジメチル硫酸塩(D−
3)ジェタノールアミンジエチル硫酸塩(Q−4)ジェ
タノールアミンジメチル硫酸塩(D−5))ジェタノー
ルアミンジメチル硫酸塩E・その他添加物 (E−1)ステアリン酸ブチルエステル(E−2)パラ
フィンワックス(融点60℃)(E−3)オクチルステ
アレート 実施例1〜7、比較例1〜5 表2に示す原料A−Eを所定量調合釜に仕込み、80〜
90℃に加熱し、同温度の温水を徐々に加えて乳化し、
25重量%濃度の乳化液を調製し試験に供した。各合成
繊維用紡績油剤の調製に用いた原料の種類、配合比及び
乳化液の安定性を表2に示す。表中、6例の「紡績性の
組成」のA−D成分の二段書きは、2種を混合している
もので、例えば実施例1てA−1を20%と、A−2を
10%とを併用することを示している。
C. Nonionic surfactant (C-1) Polyoxyethylene (n=7) Lauryl ether (C-2) Polyoxyethylene (n=25) Cetyl ether Table 1 Book: Acetate (C-3) Polyoxy Ethylene (n=25) Castor oil ether (C-4) Polyoxyethylene (n=20) Nonylphenyl ether (C-5) Polyoxyethylene (n=20) Sorbitan monolauryl ester (C-6) Polyethylene glycol (MW400) Dilaurate D/lower alkanolamine quaternary ammonium salt (D
-1) N-(2-aminoethyl)ethanol diethyl sulfate (D-2) Monoethanolamine dimethyl sulfate (D-
3) Jetanolamine diethyl sulfate (Q-4) Jetanolamine dimethyl sulfate (D-5)) Jetanolamine dimethyl sulfate E/Other additives (E-1) Butyl stearate (E-2) Paraffin wax (melting point 60°C) (E-3) Octyl stearate Examples 1 to 7, Comparative Examples 1 to 5 A predetermined amount of raw materials A to E shown in Table 2 was charged into a mixing pot, and 80 to
Heat to 90℃ and gradually add warm water at the same temperature to emulsify.
An emulsion with a concentration of 25% by weight was prepared and tested. Table 2 shows the types of raw materials, blending ratios, and stability of the emulsions used to prepare each synthetic fiber spinning oil. In the table, the two columns of components A-D in the 6 examples of "spinnable composition" indicate a mixture of two types. For example, in Example 1, 20% of A-1 and 20% of A-2 were used. 10%.

次にアクリルスフ(2dX51mm)5kgを上記油剤
の1%水溶液に浸漬(液温60℃、1分)した後、遠心
脱水機を用いて油剤水溶液の含浸量が1.5kgになる
様調製し、80℃で1時間乾燥して給油処理(乾燥後の
給油率0.3重量%)を行った。給油処理を行ったアク
リルスフを、常法に従い紡績(開綿工程−梳綿工程−粗
紡工程−精紡工程)し、1/40番手の紡績糸を得、同
時に紡績性を評価した。さらに得られた紡績糸を用いて
、その風合、染色後の風合、編成性を評価した。各性能
の評価結果を表2に示す。
Next, 5 kg of acrylic cloth (2 d x 51 mm) was immersed in a 1% aqueous solution of the above oil agent (liquid temperature 60°C, 1 minute), and then adjusted using a centrifugal dehydrator so that the amount of oil agent aqueous solution impregnated was 1.5 kg. It was dried at ℃ for 1 hour and oiled (oiling rate after drying: 0.3% by weight). The oiled acrylic fabric was spun according to a conventional method (spinning process - carding process - roving process - spinning process) to obtain a spun yarn with a count of 1/40, and the spinnability was evaluated at the same time. Furthermore, using the obtained spun yarn, its texture, texture after dyeing, and knitting properties were evaluated. Table 2 shows the evaluation results for each performance.

・紡績性の評価試験 紡績工程における静電気発生量、連条ローラーへの巻き
付き、精紡時の糸切れを測定し、紡績性を評価した。
・Evaluation test for spinnability The amount of static electricity generated during the spinning process, winding around continuous rollers, and yarn breakage during spinning were measured to evaluate spinnability.

静電気発生jl二春日電気■製集電式電位測定機を用い
、梳綿工程におけるカードウェッブの静電気発生量を測
定した。
Static electricity generation jl 2 The amount of static electricity generated in the carded web during the carding process was measured using a current collecting potential measuring device manufactured by Kasuga Denki ■.

連条ローラーへの巻き付き二連条工程における紡出スラ
イバーのフロントローラーの状態を目視にて観察し、評
価した。
The condition of the front roller of the spun sliver in the double-roll process of winding around the continuous roller was visually observed and evaluated.

精紡性:精紡工程における糸切れの回数を測定し次の基
準に従い評価した。
Spinning property: The number of yarn breaks during the spinning process was measured and evaluated according to the following criteria.

◎:精紡工程において糸切れ無し O:M紡工程において糸切れ殆ど無し △:精紡工程において糸切れが若干有り×:精紡工程に
おいて糸切れが多い ・風合評価試験 パネラ−10人のハンドリングにより、紡績糸及び染色
糸の風合を次の基準に従い評価した。
◎: No yarn breakage in the spinning process O: Almost no yarn breakage in the M spinning process △: Some yarn breakage in the spinning process ×: Many yarn breakages in the spinning process - Texture evaluation test panel - 10 people The texture of the spun yarn and dyed yarn was evaluated by handling according to the following criteria.

◎:糸の柔軟性が極めて良い Q:糸の柔軟性が良い △:糸が若干硬く、柔軟性がやや劣る ×:糸が硬く、キシミ惑が有り、柔軟性が劣る尚、紡績
糸の染色は次の条件に従った。
◎: The yarn has very good flexibility Q: The yarn has good flexibility △: The yarn is a little hard and the flexibility is a little poor ×: The yarn is hard, there is some squeamishness, and the flexibility is poor In addition, dyeing of spun yarn was subject to the following conditions:

染   料:保止ケ谷化学H製CATHILONRED
  GCLH1,0%owf 緩 染 剤ニオスピンAN    1.0%o w f
pH調製剤:酢*        0.5%o w f
酢酸ソーダ    0.5%o w f・編成性評価試
験 紡績糸を次の条件にて編成し、評価した。
Dye: CATHILONRED manufactured by Hodogaya Chemical H
GCLH1.0%owf Relaxing dye Niospin AN 1.0%owf
pH adjuster: Vinegar* 0.5% o w f
Sodium acetate 0.5%ow f Knitting property evaluation test The spun yarn was knitted under the following conditions and evaluated.

測定機:材厚計器製編成性試験機 条  件 雰囲気:25℃、40%RH 糸 速 度 :50cm/分、100m/分糸−金属摩
擦:18ゲージ編針3本、3ケ所糸−系 摩擦:2回ひ
ねり2ケ所 1回ひねり1ケ所 [発明の効果] 以上説明したように、本発明の合成繊維用紡績油剤は、
アルキルリン酸エステル塩、高級脂肪酸アミド化合物、
非イオン界面活性剤もしくはこれに低級アルカノールア
ミンの四級アンモニウム塩を特定比で含有してなるもの
で、合成繊維の紡糸工程あるいは紡績工程に用いて良好
な紡糸性、紡績性を発揮し、かつ染色後の繊維製品に優
れた風合を付与することができ、従来何種類もの工程油
剤を用いる方法に比較して、工程を簡略化することがで
きる等の効果を特徴する 特許出願人 ミヨシ油脂株式会社
Measuring device: Knitting tester manufactured by Material Thickness Gauge Conditions Atmosphere: 25°C, 40% RH Yarn speed: 50 cm/min, 100 m/min Yarn-to-metal friction: 3 18 gauge knitting needles, 3 locations Yarn-system friction: Two twists, two twists once, one twist [Effects of the invention] As explained above, the spinning oil for synthetic fibers of the present invention has the following properties:
Alkyl phosphate ester salt, higher fatty acid amide compound,
A product containing a nonionic surfactant or a quaternary ammonium salt of a lower alkanolamine in a specific ratio, and exhibits good spinnability and spinnability when used in the spinning process of synthetic fibers or the spinning process. Patent applicant Miyoshi Oil and Fat is capable of imparting an excellent texture to textile products after dyeing, and can simplify the process compared to conventional methods that use several types of process oils. Co., Ltd.

Claims (1)

【特許請求の範囲】 1、(A)アルキルリン酸エステル塩5〜80重量%、
(B)全アミン価が30以下の高級脂肪酸アミド化合物
5〜80重量%、(C)非イオン界面活性剤5〜80重
量%を含有することを特徴とする合成繊維用紡績油剤。 2、(A)アルキルリン酸エステル塩5〜80重量%、
(B)全アミン価が30以下の高級脂肪酸アミド化合物
5〜80重量%、(C)非イオン界面活性剤5〜80重
量%、(D)低級アルカノールアミンの四級アンモニウ
ム塩3〜20重量%を含有することを特徴とする合成繊
維用紡績油剤。
[Claims] 1. (A) 5 to 80% by weight of alkyl phosphate ester salt;
A spinning oil for synthetic fibers, comprising (B) 5 to 80% by weight of a higher fatty acid amide compound having a total amine value of 30 or less, and (C) 5 to 80% by weight of a nonionic surfactant. 2, (A) alkyl phosphate ester salt 5 to 80% by weight,
(B) 5-80% by weight of a higher fatty acid amide compound with a total amine value of 30 or less, (C) 5-80% by weight of a nonionic surfactant, (D) 3-20% by weight of a quaternary ammonium salt of a lower alkanolamine. A spinning oil agent for synthetic fibers, characterized by containing the following.
JP2171053A 1990-06-28 1990-06-28 Spinning oil for synthetic fibers Expired - Fee Related JP2948874B2 (en)

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JP2171053A JP2948874B2 (en) 1990-06-28 1990-06-28 Spinning oil for synthetic fibers

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JPH0457965A true JPH0457965A (en) 1992-02-25
JP2948874B2 JP2948874B2 (en) 1999-09-13

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Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH06158540A (en) * 1992-11-16 1994-06-07 Toray Ind Inc Acrylic fiber
JP2001081673A (en) * 1999-09-13 2001-03-27 Takemoto Oil & Fat Co Ltd Synthetic fiber treatment agent and synthetic fiber treatment method
JP2001207380A (en) * 2000-01-24 2001-08-03 Takemoto Oil & Fat Co Ltd Synthetic fiber treating agent for carbon fiber production and method of treating synthetic fiber for carbon fiber production
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Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH06158540A (en) * 1992-11-16 1994-06-07 Toray Ind Inc Acrylic fiber
JP2001081673A (en) * 1999-09-13 2001-03-27 Takemoto Oil & Fat Co Ltd Synthetic fiber treatment agent and synthetic fiber treatment method
JP2001207380A (en) * 2000-01-24 2001-08-03 Takemoto Oil & Fat Co Ltd Synthetic fiber treating agent for carbon fiber production and method of treating synthetic fiber for carbon fiber production
JP2008063713A (en) * 2006-08-09 2008-03-21 Matsumoto Yushi Seiyaku Co Ltd Fiber treatment agent and method for producing synthetic fiber using the same
WO2008047474A1 (en) * 2006-10-20 2008-04-24 Matsumoto Yushi-Seiyaku Co., Ltd. Fabric-treating agent, process for producing fabric, and fabric for interior material for vehicle
US8216952B2 (en) 2006-10-20 2012-07-10 Matsumoto Yushi-Seiyaku Co., Ltd. Fabric treating agent, process for producing fabric, and fabric for vehicle interior materials
JP2023136173A (en) * 2022-03-16 2023-09-29 竹本油脂株式会社 Composition containing acrylic synthetic fiber treatment agent, preparation method of diluted solution of acrylic synthetic fiber treatment agent, treatment method of acrylic synthetic fiber, and acrylic synthetic fiber
JP2025175765A (en) * 2024-05-20 2025-12-03 竹本油脂株式会社 Treatment agent for staple fibers, staple fibers, and method for producing nonwoven fabric
WO2026048965A1 (en) * 2024-08-29 2026-03-05 竹本油脂株式会社 Synthetic fiber treatment agent and synthetic fiber

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