JPS6227193B2 - - Google Patents
Info
- Publication number
- JPS6227193B2 JPS6227193B2 JP55051461A JP5146180A JPS6227193B2 JP S6227193 B2 JPS6227193 B2 JP S6227193B2 JP 55051461 A JP55051461 A JP 55051461A JP 5146180 A JP5146180 A JP 5146180A JP S6227193 B2 JPS6227193 B2 JP S6227193B2
- Authority
- JP
- Japan
- Prior art keywords
- oil
- weight
- weaving
- present
- wjl
- 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
- 238000009941 weaving Methods 0.000 claims description 18
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 5
- 239000003085 diluting agent Substances 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 150000001875 compounds Chemical class 0.000 claims description 4
- 239000004205 dimethyl polysiloxane Substances 0.000 claims description 3
- 235000013870 dimethyl polysiloxane Nutrition 0.000 claims description 3
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 3
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 229920000642 polymer Polymers 0.000 claims description 2
- 238000006116 polymerization reaction Methods 0.000 claims description 2
- 239000003921 oil Substances 0.000 description 22
- 239000003795 chemical substances by application Substances 0.000 description 10
- -1 acrylic ester Chemical class 0.000 description 8
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 7
- 150000001298 alcohols Chemical class 0.000 description 6
- 239000003292 glue Substances 0.000 description 6
- 235000014676 Phragmites communis Nutrition 0.000 description 5
- 239000000835 fiber Substances 0.000 description 5
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 4
- 238000004513 sizing Methods 0.000 description 4
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 3
- 125000002947 alkylene group Chemical group 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 2
- GJYCVCVHRSWLNY-UHFFFAOYSA-N 2-butylphenol Chemical compound CCCCC1=CC=CC=C1O GJYCVCVHRSWLNY-UHFFFAOYSA-N 0.000 description 2
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 150000001346 alkyl aryl ethers Chemical class 0.000 description 2
- 229960000541 cetyl alcohol Drugs 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
- 229940055577 oleyl alcohol Drugs 0.000 description 2
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 238000009991 scouring Methods 0.000 description 2
- NMRPBPVERJPACX-UHFFFAOYSA-N (3S)-octan-3-ol Natural products CCCCCC(O)CC NMRPBPVERJPACX-UHFFFAOYSA-N 0.000 description 1
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 1
- CYEJMVLDXAUOPN-UHFFFAOYSA-N 2-dodecylphenol Chemical compound CCCCCCCCCCCCC1=CC=CC=C1O CYEJMVLDXAUOPN-UHFFFAOYSA-N 0.000 description 1
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 244000089486 Phragmites australis subsp australis Species 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 238000006266 etherification reaction Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 125000003827 glycol group Chemical group 0.000 description 1
- 238000009499 grossing Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229940057995 liquid paraffin Drugs 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- SJWFXCIHNDVPSH-UHFFFAOYSA-N octan-2-ol Chemical compound CCCCCCC(C)O SJWFXCIHNDVPSH-UHFFFAOYSA-N 0.000 description 1
- 125000006353 oxyethylene group Chemical group 0.000 description 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 150000003333 secondary alcohols Chemical class 0.000 description 1
- 229940012831 stearyl alcohol Drugs 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
Landscapes
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Description
本発明はウオーター・ジエツト・ルーム(以下
WJLと云う)、特に合成繊維を対称とするWJL用
製織油剤に関する。
近年、製織速度の高速化に伴ない、製織油剤に
もそれに対応する性能の向上ならびに多様化が要
請されるに至つている。特に近年開発された
WJLによる製織はその製織速度が従来の方法に
比べ約3倍にもなるため、従来の製織油剤をその
まゝ使用することはできない。
以上の問題を解決するため油剤を用いて繊維―
繊維間の摩擦や繊維―織機間の摩擦を軽減させる
方法、経糸に糊付けして糸の毛羽立ちを防止する
方法等が試みられているが、今だ満足すべき方法
はない。特に油剤を用いる方法では毛羽立ちの防
止には殆んど有効でなく、むしろ糊剤を用いる場
合に比べて筬摩耗が大きくなる傾向があるため、
一般には用いられていない。
一方、糊剤を用いる方法としては例えばアクリ
ル酸エステルを成分として有する糊剤等が実用に
供されているが、糊剤は経糸に粘着性を付与する
上、温湿度の影響を受け易く製織性を阻害する傾
向がある。さらに糊剤は一般に多量に用いなけれ
ば効果がなく、しかも糸への付着は水溶液で行な
うため、製織前に乾燥する必要があり、作業効率
やエネルギー効率の点で損失が大きい。
本発明者らは糊剤を用いないで、毛羽立ちや糸
切れがなく、しかも筬摩耗の小さいWJL用製織
油剤を得るべく研究を重ねた結果、特殊な成分を
配合した非水系の油剤を用いることにより、極め
て好ましい成果の得られることを究明し、本発明
を完成した。即ち本発明は稀釈油中にジメチルポ
リシロキサン約1.5〜7.0重量%および一般式:
RO―(A―)CH2―(A′―)OR′ 〔〕
〔式中、RおよびR′は同一または異なる炭素
数4〜18のアルキル基またはアルキルアリール
基、AおよびA′は同一または異なる重合度約10
〜40のエチレンオキシドとプロピレンオキシドの
ブロツクまたはランダム重合体の残基を表わす〕
で表わされる化合物を約3〜30重量%含有するウ
オーター・ジエツト・ルーム用製織油剤に関す
る。
本発明において用いられるジメチルポリシロキ
サンは20℃における粘度が10〜30cstのものが好
ましく、油剤中の含有量は約1.5〜7.0重量%、好
ましくは2.5〜5.0重量%、特に好ましくは3.0〜
4.0重量%である。含有量が1.5重量%以下または
粘度が10cst以下の場合は筬摩耗が大きくなり、
含有量が7.0重量%以上の場合は製織後の精練性
が悪くなる傾向がある。
一般式:
RO―(A―)CH2―(A′―)OR′ 〔〕
で表わされる化合物は二塩化メチレンとアルキレ
ングリコールのモノアルキルエーテルまたはモノ
アルキルアリールエーテルとをアルカリ金属等の
存在下に反応させることにより得ることができ
る。アルキレングリコールのモノアルキルエーテ
ルまたはモノアルキルアリールエーテルはアルコ
ールやアルキルフエノール類に酸化アルキレンを
反応させることにより得られる。本発明において
好ましいエーテル化合物は炭素数4〜18のアルコ
ール類またはアルキルフエノール類に酸化エチレ
ンおよび酸化プロピレンをブロツクまたはランダ
ム共重合したものである。酸化エチレンと酸化プ
ロピレンの反応比は重量比で2:8〜6:4が好
ましく、特に3:7〜6:4が好ましい。酸化エ
チレンの比がこれより大きくなると稀釈油への溶
解性が低下し、かつこの比のバランスが崩れると
経糸の毛羽立ちが生じ易くなる。酸化アルキレン
の付加モル数の総和はA,A′それぞれ20〜80が
好ましく、特に25〜70が好ましい。酸化アルキレ
ンを付加するアルコールまたはアルキルフエノー
ル類の具体例はブチルアルコール、オクチルアル
コール、ラウリルアルコール、セチルアルコー
ル、ステアリルアルコール、オレイルアルコール
等の直鎖の飽和または不飽和アルコールの他、2
―エチルヘキサノール等の側鎖を有する合成アル
コール、sec―オクタノールのごとき第二級アル
コール、シクロヘキサノール、等の脂環式アルコ
ール、ベンジルアルコール等の含芳香核アルコー
ル、ブチルフエール、ノニルフエノール、ドデシ
ルフエノール等のアルキルフエノール類が例示さ
れる。特に好ましくは炭素数12〜18の高級アルコ
ール、ラウリルアルコール、オレイルアルコー
ル、セチルアルコール等であり、エーテル化率は
95%以上にするのが好ましい。
式〔〕で表わされるエーテル化合物におい
て、RとR′は同一でも異なつていてもよく、ま
たAとA′も同一であつても異なつていてもよ
い。該化合物は稀釈油中に約3〜30重量%、特に
好ましくは約5.0〜25.0重量%配合する。
本発明に用いる稀釈剤としては低粘度鉱物油、
例えばスピンドル油、流動パラフイン等が好適で
あるが、これに限定されるものではない。
本発明WJL用製織油剤は所要により潤滑剤、
帯電防止剤、平滑剤、乳化剤等適宜の添加剤を配
合してもよい。
本発明は従来の糊を用いた場合に比べても筬摩
耗が少く、また単に油剤をローラーに載せて糸を
走らすだけで油を付着させることができ、糊剤に
おけるごとく乾燥工程を要しない。さらに、付着
量も対繊維重量当り約1.0〜2.0重量%で十分であ
る。
本発明WJL用製織油剤は有撚糸やインターレ
ースに用いることができ、特にインターレースの
製織時に生じ易い溶融現象が抑制されるため染め
むらが生じない。また糊剤と異なり、製織途中で
油の補給(アフター・オイル)が可能である。
以下、実施例をあげて本発明を説明する。
実施例1および比較例1および2
表―1に示すWJL用製織用油剤を整経機上で
ローラータツチによりポリエステルフイラメント
(50d,24f,500回撚り)に約2.0重量%(対繊維
重量)付着させる。これを経糸として巾144cmの
WJLに7000本掛け、400rpmの速度でタフタ平織
(糸太さ;経75d、緯75d:密度:経112本/イン
チ、緯:100本/インチ)を織つた。織機の稼動
率、筬摩耗、生機品位、精練性を評価しその結果
を表―1に示した。
同様にして本発明のエーテル化合物を用いない
で得られた結果を表―1に示す。
The present invention is a water jet room (hereinafter referred to as
This product relates to weaving oils for WJL (referred to as WJL), especially for synthetic fibers. In recent years, as weaving speeds have increased, weaving oils have been required to have correspondingly improved performance and diversification. especially developed in recent years
Since the weaving speed of WJL weaving is approximately three times that of conventional methods, conventional weaving oils cannot be used as they are. In order to solve the above problems, fibers are made using an oil agent.
Attempts have been made to reduce the friction between fibers and between fibers and the loom, and to apply glue to the warp threads to prevent them from fuzzing, but no method has yet been satisfactory. In particular, methods using oil agents are hardly effective in preventing fuzzing, and in fact tend to cause greater wear on the reeds than when using glue agents.
Not commonly used. On the other hand, as a method of using a sizing agent, for example, a sizing agent containing acrylic ester as a component has been put into practical use, but the sizing agent imparts tackiness to the warp threads, is easily affected by temperature and humidity, and has poor weaving properties. tends to inhibit Furthermore, sizing agents are generally ineffective unless used in large quantities, and since they are attached to threads using an aqueous solution, they must be dried before weaving, resulting in a large loss in terms of work efficiency and energy efficiency. The present inventors have conducted extensive research to obtain a weaving oil for WJL that does not use glue, does not cause fuzzing or yarn breakage, and has less reed wear. As a result, we have found that we can use a non-aqueous oil that contains special ingredients. As a result, they discovered that very favorable results could be obtained, and completed the present invention. That is, the present invention uses about 1.5 to 7.0% by weight of dimethylpolysiloxane in diluent oil and the general formula: RO-(A-) CH2- (A'-)OR' [] [wherein R and R' are the same or Different alkyl groups or alkylaryl groups having 4 to 18 carbon atoms, A and A' are the same or different, with a degree of polymerization of about 10
~40 represents the residue of a block or random polymer of ethylene oxide and propylene oxide]
The present invention relates to a textile oil for water jet rooms containing about 3 to 30% by weight of the compound represented by: The dimethylpolysiloxane used in the present invention preferably has a viscosity of 10 to 30 cst at 20°C, and the content in the oil agent is approximately 1.5 to 7.0% by weight, preferably 2.5 to 5.0% by weight, particularly preferably 3.0 to 30% by weight.
It is 4.0% by weight. If the content is less than 1.5% by weight or the viscosity is less than 10cst, reed wear will increase.
When the content is 7.0% by weight or more, the scouring properties after weaving tend to deteriorate. The compound represented by the general formula: RO—(A—)CH 2 —(A′—)OR′ [ ] is produced by combining methylene dichloride and monoalkyl ether or monoalkylaryl ether of alkylene glycol in the presence of an alkali metal, etc. It can be obtained by reaction. Monoalkyl ether or monoalkylaryl ether of alkylene glycol can be obtained by reacting alcohol or alkylphenols with alkylene oxide. Preferred ether compounds in the present invention are those obtained by block or random copolymerization of alcohols or alkylphenols having 4 to 18 carbon atoms with ethylene oxide and propylene oxide. The reaction ratio of ethylene oxide and propylene oxide is preferably 2:8 to 6:4, particularly preferably 3:7 to 6:4, by weight. If the ratio of ethylene oxide is larger than this, the solubility in diluent oil will decrease, and if the balance of this ratio is lost, the warp threads will tend to become fluffy. The total number of moles of alkylene oxide added is preferably 20 to 80 for each of A and A', particularly preferably 25 to 70. Specific examples of alcohols or alkylphenols to which alkylene oxide is added include straight chain saturated or unsaturated alcohols such as butyl alcohol, octyl alcohol, lauryl alcohol, cetyl alcohol, stearyl alcohol, oleyl alcohol, etc.
-Synthetic alcohols with side chains such as ethylhexanol, secondary alcohols such as sec-octanol, alicyclic alcohols such as cyclohexanol, aromatic nuclear alcohols such as benzyl alcohol, butyl phenol, nonylphenol, dodecylphenol, etc. Examples include alkylphenols. Particularly preferred are higher alcohols having 12 to 18 carbon atoms, lauryl alcohol, oleyl alcohol, cetyl alcohol, etc., and the etherification rate is
It is preferable to set it to 95% or more. In the ether compound represented by the formula [], R and R' may be the same or different, and A and A' may also be the same or different. The compound is incorporated in the diluent oil in an amount of about 3 to 30% by weight, particularly preferably about 5.0 to 25.0% by weight. Diluents used in the present invention include low viscosity mineral oil;
For example, spindle oil, liquid paraffin, etc. are suitable, but are not limited thereto. The weaving oil for WJL of the present invention can be used as a lubricant if necessary.
Appropriate additives such as antistatic agents, smoothing agents, emulsifiers, etc. may be blended. The present invention has less reed wear compared to the case of using conventional glue, and the oil can be attached by simply placing the oil on a roller and running the thread, and does not require a drying process unlike the case of glue. Furthermore, a coating amount of approximately 1.0 to 2.0% by weight based on the weight of the fibers is sufficient. The weaving oil for WJL of the present invention can be used for twisted yarns and interlace, and in particular, it suppresses the melting phenomenon that tends to occur when weaving interlace, so uneven dyeing does not occur. Also, unlike glue, it is possible to replenish oil during weaving (after-oil). The present invention will be explained below with reference to Examples. Example 1 and Comparative Examples 1 and 2 Approximately 2.0% by weight (based on fiber weight) of the WJL weaving oil shown in Table 1 was applied to polyester filaments (50d, 24f, 500 twists) by roller touch on a warping machine. let Use this as the warp to create a width of 144cm.
A plain taffeta weave (thread thickness: warp 75d, weft 75d; density: warp 112 threads/inch, weft: 100 threads/inch) was woven using 7,000 threads on WJL at a speed of 400 rpm. The operating rate of the loom, reed wear, gray fabric quality, and scouring properties were evaluated and the results are shown in Table 1. Table 1 shows the results obtained in the same manner without using the ether compound of the present invention.
【表】【table】
【表】
実施例2および比較例3
表―2に示すWJL用製織用油剤を整経機上で
ローラータツチによりナイロンフイラメント
(70d,17f,インターレース糸)に約1.5重量%付
着させた後、これを経糸として巾144cmのWJLに
8500本掛け400rpmの速度で製織した。得られた
結果を表―2に示す。なお本発明のエーテル化合
物を含有しない油剤を用いて同様に製織した結果
を比較例3として示す。[Table] Example 2 and Comparative Example 3 Approximately 1.5% by weight of the WJL weaving oil shown in Table 2 was applied to nylon filament (70d, 17f, interlaced yarn) using a roller touch on a warping machine. into a WJL with a width of 144 cm as the warp.
It was woven at a speed of 400 rpm with 8,500 threads. The results obtained are shown in Table 2. Comparative Example 3 shows the results of similar weaving using an oil agent that does not contain the ether compound of the present invention.
【表】
なお実施例中、EOはオキシエチレン基、POは
ポリオキシエチレン残基およびPEGはポリエチ
レングリコール残基を示す。[Table] In the examples, EO represents an oxyethylene group, PO represents a polyoxyethylene residue, and PEG represents a polyethylene glycol residue.
Claims (1)
7.0重量%および一般式: RO―(A―)CH2―(A′―)OR′ 〔〕 〔式中、RおよびR′は同一または異なる炭素
数4〜18のアルキル基またはアルキルアリール
基、AおよびA′は同一または異なる、重合度約
10〜40のエチレンオキシドとプロピオンオキシド
のブロツクまたはランダム重合体の残基を表わ
す〕で表わされる化合物を約3〜30重量%含有す
るウオーター・ジエツト・ルーム用製織油剤。[Claims] 1. Dimethylpolysiloxane in diluent oil from about 1.5 to
7.0% by weight and general formula: RO-(A-) CH2- (A'-)OR' [] [In the formula, R and R' are the same or different alkyl groups or alkylaryl groups having 4 to 18 carbon atoms, A and A′ are the same or different, the degree of polymerization is approximately
A weaving oil for water jet looms containing about 3 to 30% by weight of a compound represented by 10 to 40 residues of a block or random polymer of ethylene oxide and propion oxide.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5146180A JPS56148973A (en) | 1980-04-17 | 1980-04-17 | Oil agent for making fabric |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5146180A JPS56148973A (en) | 1980-04-17 | 1980-04-17 | Oil agent for making fabric |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS56148973A JPS56148973A (en) | 1981-11-18 |
JPS6227193B2 true JPS6227193B2 (en) | 1987-06-12 |
Family
ID=12887569
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP5146180A Granted JPS56148973A (en) | 1980-04-17 | 1980-04-17 | Oil agent for making fabric |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS56148973A (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS59144682A (en) * | 1983-01-28 | 1984-08-18 | 日華化学工業株式会社 | Oil agent composition |
JPH0765271B2 (en) * | 1986-05-22 | 1995-07-12 | ユニチカ株式会社 | Method for producing antifouling curing sheet |
-
1980
- 1980-04-17 JP JP5146180A patent/JPS56148973A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS56148973A (en) | 1981-11-18 |
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