JPS6099074A - Oil agent for knitted cloth - Google Patents
Oil agent for knitted clothInfo
- Publication number
- JPS6099074A JPS6099074A JP58205575A JP20557583A JPS6099074A JP S6099074 A JPS6099074 A JP S6099074A JP 58205575 A JP58205575 A JP 58205575A JP 20557583 A JP20557583 A JP 20557583A JP S6099074 A JPS6099074 A JP S6099074A
- Authority
- JP
- Japan
- Prior art keywords
- parts
- oil agent
- acid
- textile
- alkylene oxide
- 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
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/285—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acid amides or imides
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
- D06M13/402—Amides imides, sulfamic acids
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
本発明は編織用油剤に関するものであシ、更に詳しくは
繊維製品の加工工程である編織工程を円滑化し、編織物
の品質を向上させるために用いられるポリオキシアルキ
レン脂肪酸アミド型非イオン性界面活性剤を含有する編
織用油剤に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a textile oil, and more specifically to a polyoxyalkylene fatty acid used to smooth the textile process, which is a textile processing process, and to improve the quality of textiles. The present invention relates to a textile oil containing an amide type nonionic surfactant.
編織用油剤は繊維(紡績糸など)に優れた平滑性、防電
性、柔軟性を付与し、編織工程中に繊維に加えられる外
方が繊維を損傷することを防止している。この編織用油
剤は繊維表面に層をなして吸着し、その効果を発現して
いる。又m@用油剤は、繊維表面に付着させる工程にお
いては水溶液又は乳化分散状態で用いられる。Textile oils provide fibers (spun yarn, etc.) with excellent smoothness, electrical resistance, and flexibility, and prevent damage to the fibers from external substances added to the fibers during the textile process. This textile oil is adsorbed in a layer on the fiber surface and exerts its effect. In addition, the m@ oil agent is used in the form of an aqueous solution or an emulsified dispersion state in the process of adhering it to the fiber surface.
従来、かかる編織用油剤として、炭化水素ワックスまた
は天然或いは合成ワックスなどを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ポリオキシプロビレング
リコール、グリセリン脂肪酸エステル、ソルビタン脂肪
酸エステル、ポリオキシエチレンソルビタン脂肪酸エス
テルなどの非イオン性界面活性剤などで乳化分散させた
ものを用いうることは公知であるが、編織用油剤として
利用可能な程度に安定な乳化分散液を得るためには、該
乳化分散液中のワックスの含有量を充分に多くすること
ができず、そのために、充分な性能(平滑性など)を付
与し得なかった。Conventionally, hydrocarbon waxes, natural or synthetic waxes, etc. have been used as oils for textiles, polyoxyethylene alkyl ethers, polyoxyethylene alkyl phenyl ethers, polyoxyethylene polyoxyprobylene glycol, glycerin fatty acid esters, sorbitan fatty acid esters, polyoxy It is well known that it is possible to use emulsified dispersions with nonionic surfactants such as ethylene sorbitan fatty acid esters, but in order to obtain emulsified dispersions that are stable enough to be used as textile oils, it is necessary to The content of wax in the emulsified dispersion could not be increased sufficiently, and therefore sufficient performance (smoothness, etc.) could not be imparted.
また、平滑性を満足しても、防電性や柔軟性が、劣って
いたルして実用性に問題があった。In addition, even if the smoothness was satisfied, the electrical resistance and flexibility were poor and there were problems with practicality.
更に、平滑性、防電性、柔軟性を満足しても、乳化安定
性が劣シ、繊維表面に付着させる工程において、乳化安
定性(ポンプによる処理浴の強制循環などで、機械的衝
撃により乳化分散粒子が破壊されること)に問題があっ
たシして、総合的に上記諸性能を満足するものはなかっ
た。Furthermore, even if smoothness, electrical resistance, and flexibility are satisfied, the emulsion stability is poor, and in the process of attaching it to the fiber surface, the emulsion stability (forced circulation of the treatment bath with a pump, etc.) However, there was a problem with the destruction of the emulsified dispersed particles, and there was no product that comprehensively satisfied the above performance.
これらの事情から、本発明者らは、鋭意研究の結果、特
定の非イオン性界面活性剤を用いると極めて安定な乳化
分散液が得られ、なおかつ上記諸性能を繊維に対し伺与
できることを見い出し本発明に到達した。In light of these circumstances, the present inventors have conducted extensive research and discovered that an extremely stable emulsified dispersion can be obtained by using a specific nonionic surfactant, and that the above-mentioned properties can also be imparted to fibers. We have arrived at the present invention.
すなわち、本発明は炭素数8〜24の高級脂肪酸と一般
式(11
%式%(
C式中、nは1〜3の整数、mは2〜9の整数・ を表
わす。)
で表わされるポリアルキレンポリアミンを脱水縮合して
得られるアミド化合物にアルキレンオキサイドを付加反
応して得られる非イオン性界面活性剤を含有することを
特徴とする編織用油剤を提供するものである。That is, the present invention is based on a higher fatty acid having 8 to 24 carbon atoms and a polyester represented by the general formula (11% formula % (in formula C, n is an integer of 1 to 3, and m is an integer of 2 to 9). The present invention provides a textile oil containing a nonionic surfactant obtained by adding an alkylene oxide to an amide compound obtained by dehydration condensation of an alkylene polyamine.
本発明に係る炭素数8〜24の高級脂肪酸としては、飽
和又は不飽和のいずれでも使用でき、各種脂肪酸の混合
物であってもよい。これらの脂肪酸としては例えばカプ
リル酸、カプリン酸、ラウリン酸、パルミチン酸、ステ
アリン酸、ベヘニン酸等の飽和脂肪酸、オレイン酸等の
不飽和脂肪酸、ヤシ油脂肪酸、パーム油脂肪酸、牛脂脂
肪酸等の混合脂肪酸を挙げることができる・なかでもス
テアリン酸、ベヘニン酸が好ましい。The higher fatty acid having 8 to 24 carbon atoms according to the present invention may be either saturated or unsaturated, and may be a mixture of various fatty acids. Examples of these fatty acids include saturated fatty acids such as caprylic acid, capric acid, lauric acid, palmitic acid, stearic acid, and behenic acid, unsaturated fatty acids such as oleic acid, and mixed fatty acids such as coconut oil fatty acid, palm oil fatty acid, and beef tallow fatty acid. Among them, stearic acid and behenic acid are preferred.
一般式(Ilで表わされるポリアルキレンポリアミンと
しては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などを挙げることができる
。Examples of the polyalkylene polyamine represented by the general formula (Il) include diethylenetriamine, triethylenetetramine, and tetraethylenepentamine.
高級脂肪酸とポリアルキレンポリアミンのモル比は3/
1〜1/1が好ましい。The molar ratio of higher fatty acid and polyalkylene polyamine is 3/
1 to 1/1 is preferable.
縮合反応は、120〜200Cで脱水しながら行なう。The condensation reaction is carried out at 120 to 200C while being dehydrated.
必要に応じベンゼン、トルエン等の溶媒が用いられる。A solvent such as benzene or toluene is used if necessary.
脱水は共沸、減圧、精留によシなされる。Dehydration is accomplished by azeotropy, reduced pressure, or rectification.
アルキレンオキサイドとしてはエチレンオキサイドのほ
か、エチレンオキサイドとプロピレンオキサイドまたは
ブチレンオキサイドとの混合アルキレンオキサイド(ラ
ンダム、ブロックを問わない)であってもよい。但し、
混合アルキレンオキサイドにあってはエチレンオキサイ
ドが50重分%以上であることが必要である。In addition to ethylene oxide, the alkylene oxide may be a mixed alkylene oxide (regardless of random or block) of ethylene oxide and propylene oxide or butylene oxide. however,
In the mixed alkylene oxide, it is necessary that the ethylene oxide content is 50% by weight or more.
乳化安定性の点からエチレンオキサイド単独が特に好ま
しい。From the viewpoint of emulsion stability, ethylene oxide alone is particularly preferred.
アルキレンオキサイドの付加モル数は、出発ポリアルキ
レンポリアミン1モルに対し1〜50モル、好ましくは
3〜30モルである。The number of moles of alkylene oxide added is 1 to 50 moles, preferably 3 to 30 moles, per mole of the starting polyalkylene polyamine.
付加反応は公知の方法で行なわれる。例えばアルカリ触
媒の存在下に縮合アミド化合物に130〜170Cでア
ルキレンオキサイドを吹込むことによシ行なわれる。The addition reaction is carried out by a known method. For example, this is carried out by blowing alkylene oxide into the condensed amide compound at 130 to 170 C in the presence of an alkali catalyst.
本発明の編織用油剤組成物中の非イオン性界面活性剤(
アミド化合物のアルキレンオキサイド付加物)の含有量
は1〜50重量%が好ましく、更に好ましくは5〜30
重量%である。又、本発明の編織用油剤組成物中には上
記非イオン性界面活性剤の他に鉱物油、合成エステル等
の平滑成分が配合される。この平滑成分の組成物中の含
有量は5〜50重量%が好ましく、更に好ましくは10
〜40重量%である。The nonionic surfactant (
The content of alkylene oxide adducts of amide compounds is preferably 1 to 50% by weight, more preferably 5 to 30% by weight.
Weight%. In addition to the above nonionic surfactant, the textile oil composition of the present invention contains smoothing components such as mineral oil and synthetic ester. The content of this smooth component in the composition is preferably 5 to 50% by weight, more preferably 10% by weight.
~40% by weight.
本発明の編織用油剤を繊維に処理する際には、上記非イ
オン性界面活性剤0.5〜2011/13、平滑成分1
〜too#/4の濃度の乳化水溶液として処理するのが
好ましい。When treating fibers with the textile oil of the present invention, the above-mentioned nonionic surfactant 0.5 to 2011/13, smoothing component 1
It is preferable to process as an emulsified aqueous solution with a concentration of ~too#/4.
本発明に係る非イオン性界面活性剤はそれのみで乳化性
、帯電防止性、風合い(柔軟性)を与えるが、必要に応
じ他の乳化剤、帯電防止剤の配合を何らさまたげるもの
ではない。The nonionic surfactant according to the present invention provides emulsifying properties, antistatic properties, and texture (softness) by itself, but this does not preclude the addition of other emulsifiers and antistatic agents as necessary.
本発明の編織用油剤によシ処理される繊維は天然、合成
のいずれの繊維であってもよく、ウール、アクリル、ポ
リエステル、ポリアミド、綿、あるいはそれらの混合繊
維などが例示される。The fibers treated with the textile oil of the present invention may be either natural or synthetic fibers, and include wool, acrylic, polyester, polyamide, cotton, and mixed fibers thereof.
以下、本発明を具体的に明らかにすべく、実施例をあげ
て説明するが、本発明は、これらの実施例に限定される
ものではない。実施例中の部は重量部を示す。EXAMPLES Hereinafter, in order to specifically clarify the present invention, the present invention will be described with reference to Examples, but the present invention is not limited to these Examples. Parts in Examples indicate parts by weight.
合成例
温度計、攪拌機、ガス吹込管及び脱水冷却管を付した2
J−四ツロフラスコにベヘニン酸857.5 、P C
1,8モル)を入れ、窒素置換後、90Cに昇温し、ジ
エチレントリアミン150II(1,0モル)を20分
間で滴下し、135〜145Cに保ちながら6時間脱水
縮合を行った。Synthesis Example 2 with thermometer, stirrer, gas blowing pipe and dehydration cooling pipe
Behenic acid 857.5 in J-Yoturo flask, P C
After purging with nitrogen, the temperature was raised to 90C, diethylenetriamine 150II (1.0 mol) was added dropwise over 20 minutes, and dehydration condensation was carried out for 6 hours while maintaining the temperature at 135 to 145C.
次に、温度155tl’に保ち、水酸化カリウム1.5
9を加え、エチレンオキサイドを1時間力)け5B6.
019(10モル)吹き込み反応を終了した。Next, the temperature was maintained at 155 tl', and potassium hydroxide was 1.5
Add 9 and apply ethylene oxide for 1 hour) 5B6.
019 (10 mol) was added to complete the reaction.
次に、90 C/ 100 tlla Hg abs
以下にて30分間脱気を行い窒素で常圧にもどし、酢酸
1.61を用いて中和し、反応生成物を得た。反応生成
物の分析値は下記の通シであった。Next, 90 C/ 100 tlla Hg abs
The reaction mixture was degassed for 30 minutes, returned to normal pressure with nitrogen, and neutralized with 1.61% acetic acid to obtain a reaction product. The analytical values of the reaction products were as follows.
酸価(AV) = 0.54、水酸基価(OHV) =
150.8、トータルアミン価(ToAmV) =
67.0こうして得られた非イオン性界面活性剤を用い
て実施例1を行った。以下、このようにして得られた非
イオン性界面活性剤を次のように表示する。Acid value (AV) = 0.54, hydroxyl value (OHV) =
150.8, total amine value (ToAmV) =
67.0 Example 1 was carried out using the nonionic surfactant thus obtained. Hereinafter, the nonionic surfactant thus obtained will be expressed as follows.
ジエチレントリアミン/ベヘニン酸(1: 1.8)・
10EO付加物
実施例1
イ) パラフィンワツク、c(m、p57p) 50.
0部0) ジエチレントリアミン/ベヘニン酸(1:1
.8)・10EO付加物 15.0部
ノ9 水 55.0部
上記イ)、噂を乳化槽に投入し、90〜100C0で溶
解し均一にする。次いで槽内を80〜90Cに保ち約8
0Cの湯を徐々に連続的に投入し乳化分散せしめ完全均
一とする。全ての湯を投入後、徐々に冷却し乳化分散液
(固型分45%)を得た。Diethylenetriamine/behenic acid (1: 1.8)・
10EO adduct Example 1 a) Paraffin wax, c(m, p57p) 50.
0 parts 0) diethylenetriamine/behenic acid (1:1
.. 8)・10 EO adduct 15.0 parts No. 9 Water 55.0 parts Add the above (a) and the ingredients into an emulsification tank, and dissolve at 90 to 100 C0 to make it homogeneous. Next, keep the inside of the tank at 80 to 90C for about 8
0C hot water is gradually and continuously added to emulsify and disperse the emulsion to make it completely uniform. After all of the hot water was added, the mixture was gradually cooled to obtain an emulsified dispersion (solid content: 45%).
以下実施例2.3、比較例1〜5も実施例1と同様の方
法で乳化分散を行い乳化分散液を得た。In Examples 2.3 and Comparative Examples 1 to 5, emulsification and dispersion were carried out in the same manner as in Example 1 to obtain emulsified dispersions.
実施例2
イ) パラフィンワックス(m、p57C) 40.0
部1:I))!Jエチレンテトラミン/ベヘニン酸(1
:1.8)・5PO・15EO付加物 5.0部
ノ9 水 55.0部
(ωPOはプロピレンオキサイドを示す。Example 2 a) Paraffin wax (m, p57C) 40.0
Part 1: I))! J ethylenetetramine/behenic acid (1
:1.8)・5PO・15EO adduct 5.0 parts-9 Water 55.0 parts (ωPO indicates propylene oxide.
実施例3
イ) パラフィンワックス(a+、p57t) 20.
0部司 ソルビタンモノステアレー) to、ofmノ
1) ジエチレントリアミン/ベヘニン酸(1:1.8
)・151EO付加物 15.0部
に)水 55.0部
比較例1
イ) パラフィンワックス(m、p57c) so、o
部す オレイルアルコール・6EO付加物 15.0部
/″)水 55.0部
比較例2
イ) パラフィンワックスCrtr、p57C) 30
.0部す ノニルフェノール・6KO付加物 15.0
部ノ9 水 55.0部
比較例3
イ) パラフィンワツクx(+a、p57C) 20.
0部す ソルビタンモノステアレー) to、ofJノ
)) オレイルアルコール・15ICo付加物 15.
0部品)水 55.0部
比較例4
イ) パラフィンワックス(m、I)57tll’)
20.0部口) ソルビタンモノステアレー) 10−
0部ノ9 ソルビタンモノオレエート・zogo付加物
15.0部品)水 55.0部
比較例5
イ) パラフィンワックス(m、p57c) 7.0部
1:I) ソルビタンモノステアレート to、’og
ノ9 ソルビタンモノオレエート・20EO付加物 1
5.0部→ 水 68.o部
実施例4
実施例1〜5及び比較例1〜5で得た乳化分散液の特性
を調べ表1に示した。Example 3 a) Paraffin wax (a+, p57t) 20.
Sorbitan monostearate) to, ofm 1) diethylenetriamine/behenic acid (1:1.8
)・151EO adduct 15.0 parts) water 55.0 parts Comparative Example 1 a) Paraffin wax (m, p57c) so, o
Oleyl alcohol/6EO adduct 15.0 parts/'') Water 55.0 parts Comparative Example 2 a) Paraffin wax Crtr, p57C) 30
.. 0 parts Nonylphenol/6KO adduct 15.0
Part 9 Water 55.0 parts Comparative Example 3 a) Paraffin wash x (+a, p57C) 20.
0 parts Sorbitan monostearate) to, ofJノ)) Oleyl alcohol/15ICo adduct 15.
0 parts) Water 55.0 parts Comparative Example 4 a) Paraffin wax (m, I) 57tll')
20.0 parts) Sorbitan monostear) 10-
0 parts no 9 Sorbitan monooleate/zogo adduct 15.0 parts) Water 55.0 parts Comparative example 5 a) Paraffin wax (m, p57c) 7.0 parts 1:I) Sorbitan monostearate to,'og
No. 9 Sorbitan monooleate/20EO adduct 1
5.0 parts → water 68. Part o Example 4 The characteristics of the emulsified dispersions obtained in Examples 1 to 5 and Comparative Examples 1 to 5 were investigated and shown in Table 1.
表 1
1 判定基準
O:液状
Δ:軟ペースト状
×:硬固林状
蒼2 乳化分散液の101/Jiの溶液を調整し、その
溶液を電気ミキサー(松下を器産業株式会社製、MX−
(S4OG形)にて5分間攪拌して評価
O:分散粒子の凝集がない
Δ: I がやや凝集する
×: l が凝集する
実施例5
実施例1〜3及び比較例1〜5で得た乳化分散液の編織
用油剤としての特性を訴べ表2に示した。Table 1 1 Judgment criteria O: Liquid Δ: Soft paste x: Hard forest blue 2 A 101/Ji solution of the emulsified dispersion was prepared, and the solution was mixed with an electric mixer (manufactured by Matsushita Oki Sangyo Co., Ltd., MX-
(S4OG type) for 5 minutes and evaluated: O: No aggregation of dispersed particles Δ: Slight aggregation of I ×: Aggregation of l Example 5 Obtained in Examples 1 to 3 and Comparative Examples 1 to 5 Table 2 shows the characteristics of the emulsified dispersion as an oil for textiles.
表 2
利 各側で得られた乳化分散液をチーズ染色機(日本染
色機誠株式会社)を用い、ポリエステル/木綿混紡糸に
5I/2水溶液で付着i0.5%(対繊維)になるよう
に処1し、80Cで1時間乾燥した後20tl:’45
%相対湿度(R,H)で24時間調湿した後、μメータ
ー(エイコー測器株式会社)の摩擦部分に編針を3本セ
ットし、糸とフック部分のJi!擦を糸速50.100
.150.200 m / lll1nに変速した時の
各糸速での摩擦抵抗の合計値を示す。抵抗値が低い方が
平滑性は良好。Table 2: The emulsified dispersion obtained on each side was attached to the polyester/cotton blend yarn using a 5I/2 aqueous solution using a cheese dyeing machine (Nihon Senki Makoto Co., Ltd.) to give an i of 0.5% (based on the fiber). After drying at 80C for 1 hour, 20tl:'45
After conditioning the humidity at % relative humidity (R, H) for 24 hours, set three knitting needles on the friction part of a μ meter (Eiko Sokki Co., Ltd.) and check the Ji! Thread speed 50.100
.. The total value of frictional resistance at each yarn speed when changing speed to 150.200 m/lll1n is shown. The lower the resistance value, the better the smoothness.
斧2 斧1と同じ方法で20 Om / winでの糸
とフック部分の摩擦直後に糸の表面に発生した静電気を
集電式電位測定器(春日電機株式会社)にて測定した値
を示す。電圧が0に近い方が防電性は良好。Ax 2 The static electricity generated on the thread surface immediately after friction between the thread and the hook part at 20 Om/win was measured using a current collector potential measuring device (Kasuga Denki Co., Ltd.) using the same method as Ax 1. The closer the voltage is to 0, the better the electrical protection.
黄5 養1で処理した糸を10絵糸九編機〔株式会社小
池機械製作所〕を用いて編地を作成し官能評価した。A knitted fabric was prepared using a 10-picture thread 9 knitting machine (Koike Kikai Seisakusho Co., Ltd.) using the yarn treated with Yellow 5 and Nutrition 1, and was subjected to sensory evaluation.
判定基準 ○:柔らかい Δ:やや硬い X:硬い 出願人代理人 古 谷 馨Judgment criteria ○:Soft Δ: Slightly hard X: hard Applicant's agent Kaoru Furutani
Claims (1)
fCOH2)n−11H9,H(1)(式中、nは1〜
3の整数、mは2〜9の整数を表わす。) で表わされるポリアルキレンポリアミンを脱水縮合して
得られるアミド化合物にアルキレンオキサイドを付加反
応して得られる非イオン性界面活性剤を含有することを
特徴とする編織用油剤。 2 アルキレンオキサイドの付加モル数がポリアルキレ
ンポリアミン1モルに対し3〜30モルである特許請求
の範囲第1項記載の編織用油剤。[Claims] 1. Higher fatty acid having 8 to 24 carbon atoms and general formula (!) H2H
fCOH2)n-11H9,H(1) (where n is 1 to
An integer of 3 and m represent an integer of 2 to 9. ) A textile oil agent characterized by containing a nonionic surfactant obtained by addition-reacting an alkylene oxide to an amide compound obtained by dehydration condensation of a polyalkylene polyamine represented by: 2. The textile oil agent according to claim 1, wherein the number of moles of alkylene oxide added is 3 to 30 moles per mole of polyalkylene polyamine.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58205575A JPS6099074A (en) | 1983-10-31 | 1983-10-31 | Oil agent for knitted cloth |
KR1019840006325A KR910000525B1 (en) | 1983-10-31 | 1984-10-12 | Finishing agent of fiber or it's goods |
ES537188A ES537188A0 (en) | 1983-10-31 | 1984-10-29 | A PROCEDURE FOR THE PREPARATION OF SURFACTANTS DERIVED FROM POLYALKYLENE POLYAMIDES. |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP58205575A JPS6099074A (en) | 1983-10-31 | 1983-10-31 | Oil agent for knitted cloth |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS6099074A true JPS6099074A (en) | 1985-06-01 |
Family
ID=16509153
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP58205575A Pending JPS6099074A (en) | 1983-10-31 | 1983-10-31 | Oil agent for knitted cloth |
Country Status (2)
Country | Link |
---|---|
JP (1) | JPS6099074A (en) |
KR (1) | KR910000525B1 (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63274449A (en) * | 1987-05-01 | 1988-11-11 | Kao Corp | Wax emulsion |
US5011630A (en) * | 1985-06-07 | 1991-04-30 | National Starch And Chemical Investment Holding Corporation | Emulsifiable triglyceride compositions |
US5030388A (en) * | 1985-06-07 | 1991-07-09 | National Starch And Chemical Investment Holding Corporation | Emulsifiable triglyceride compositions |
JPH0949166A (en) * | 1995-08-01 | 1997-02-18 | Chisso Corp | Durable hydrophilic fiber, cloth-like body and formed body |
JPH0978340A (en) * | 1995-09-11 | 1997-03-25 | Mitsubishi Rayon Co Ltd | Acrylic fiber of carbon fiber precursor |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5567068A (en) * | 1978-11-09 | 1980-05-20 | Takemoto Oil & Fat Co Ltd | Oil agent for spun yarn |
-
1983
- 1983-10-31 JP JP58205575A patent/JPS6099074A/en active Pending
-
1984
- 1984-10-12 KR KR1019840006325A patent/KR910000525B1/en not_active IP Right Cessation
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5567068A (en) * | 1978-11-09 | 1980-05-20 | Takemoto Oil & Fat Co Ltd | Oil agent for spun yarn |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5011630A (en) * | 1985-06-07 | 1991-04-30 | National Starch And Chemical Investment Holding Corporation | Emulsifiable triglyceride compositions |
US5030388A (en) * | 1985-06-07 | 1991-07-09 | National Starch And Chemical Investment Holding Corporation | Emulsifiable triglyceride compositions |
JPS63274449A (en) * | 1987-05-01 | 1988-11-11 | Kao Corp | Wax emulsion |
JPH0949166A (en) * | 1995-08-01 | 1997-02-18 | Chisso Corp | Durable hydrophilic fiber, cloth-like body and formed body |
JPH0978340A (en) * | 1995-09-11 | 1997-03-25 | Mitsubishi Rayon Co Ltd | Acrylic fiber of carbon fiber precursor |
Also Published As
Publication number | Publication date |
---|---|
KR910000525B1 (en) | 1991-01-26 |
KR850003448A (en) | 1985-06-17 |
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