JPS6112979A - Transfer inhibiting agent - Google Patents

Transfer inhibiting agent

Info

Publication number
JPS6112979A
JPS6112979A JP59133533A JP13353384A JPS6112979A JP S6112979 A JPS6112979 A JP S6112979A JP 59133533 A JP59133533 A JP 59133533A JP 13353384 A JP13353384 A JP 13353384A JP S6112979 A JPS6112979 A JP S6112979A
Authority
JP
Japan
Prior art keywords
emulsion
resin
present
compound
parts
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
Application number
JP59133533A
Other languages
Japanese (ja)
Inventor
大石 博
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.)
Sanyo Chemical Industries Ltd
Original Assignee
Sanyo Chemical Industries 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 Sanyo Chemical Industries Ltd filed Critical Sanyo Chemical Industries Ltd
Priority to JP59133533A priority Critical patent/JPS6112979A/en
Publication of JPS6112979A publication Critical patent/JPS6112979A/en
Pending legal-status Critical Current

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  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Nonwoven Fabrics (AREA)

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】 本発明は樹脂エマルション移行防止剤に関するものであ
る。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a resin emulsion migration inhibitor.

現在樹脂エマルションは織布、不織布等の繊維製品に処
理され樹脂加工、レザー、バインダー等の用途に数多く
使用されて゛いる。樹脂エマルションの使用方法として
は浸漬、スプレー、′コニティング等ある。本発明の移
行防止剤は、繊維製品が樹脂エマルションによってぬら
され乾燥jる加工方法において、乾燥時に生ずる樹脂エ
マルション粒子が繊維製品の極部(例えば表面など乾燥
の早い部分)に移行するのを防止するものである計通か
繊維に゛樹脂エマルションを含浸させ乾燥させる方法で
は、特に厚手の繊維製品の場合に樹脂の移行が顕著に表
われ、繊維製品の表面付近に樹脂が集中した状態とな゛
す、風合は硬く、ドレープ性が無くなる等の欠点が  
  “あった。
Currently, resin emulsions are processed into textile products such as woven fabrics and non-woven fabrics, and are used in many applications such as resin processing, leather, and binders. Methods for using resin emulsions include dipping, spraying, and conniting. The migration inhibitor of the present invention prevents the resin emulsion particles generated during drying from migrating to the extreme parts of the textile product (for example, areas that dry quickly such as the surface) in a processing method in which the textile product is wetted with a resin emulsion and then dried. In the method of impregnating fibers with a resin emulsion and drying them, the migration of the resin is particularly noticeable in the case of thick textile products, and the resin is concentrated near the surface of the textile product. However, there are disadvantages such as the texture is hard and the drapability is lost.
"there were.

本発明者等はそういった欠点を無くする為に種々検討し
た結果 一般式 ; XO±A O+Tr−Y 〔ただしA;エチレン基、またはこれを主体とする炭素
数2〜4個のアルキレン基、n′ ;50〜700、X
、YlまたはR−Co、R;炭素数7〜22の炭化水素
基〕 を有する化合物を樹脂エマルションに加えて繊維製品を
樹脂エマルション加工する場合に、繊維製品の内部にま
で均一に樹脂が付着し且つ、風合、ドレープ性も良好と
なることを見い出し本発明に到った。一般式で表わされ
る水溶性の化合物は従来染料および顔料捺染の捺染糊お
よび捺染糊用増粘剤としては既に公知であるが、その使
用量は増粘が必要であるため、糊液中3〜10%程度で
染料、顔料等に対しては30〜800%と非常に多い。
The inventors of the present invention conducted various studies in order to eliminate such drawbacks, and as a result, the general formula: ;50-700,X
, Yl or R-Co, R; hydrocarbon group having 7 to 22 carbon atoms] When processing a textile product with a resin emulsion by adding a compound having the following, the resin adheres uniformly to the inside of the textile product. In addition, it was discovered that the hand and drape properties were also improved, leading to the present invention. The water-soluble compound represented by the general formula is already known as a printing paste for conventional dye and pigment printing and as a thickener for printing paste. It is about 10%, but for dyes, pigments, etc., it is very high at 30-800%.

 本発明では樹脂エマルションを均一に繊維製品に付着
せしめる必要があるため、処理液を捺染糊のように粘度
を高くさせてはならず、粘度は低く保たしめる使用量の
範囲で使用する。一般式の化合物を具体的に説明すると
、エチレンオキシド単独またはエチレンオキシドを主体
としたプロピレンオキシド、およびブチレンオキシドの
共重合物からなるポリアルキレングリコールと炭素数7
〜22の高級アルコール、高級脂肪酸およびアルキルフ
ェノールトノエーテル、エステル、エーテルエステル化
合物であり、これらの具体例は特公昭45−38826
号、特公昭46−1592号、および特公昭51−1’
1272号明細書に増粘剤として開示される化合物力t
よい。
In the present invention, since it is necessary to uniformly adhere the resin emulsion to the textile product, the viscosity of the treatment liquid must not be made high like that of printing paste, and the viscosity is used within a range that keeps the viscosity low. To specifically explain the compound of the general formula, it is a polyalkylene glycol consisting of ethylene oxide alone, propylene oxide mainly composed of ethylene oxide, and a copolymer of butylene oxide, and a carbon number 7.
~22 higher alcohols, higher fatty acids, and alkylphenol tonoether, ester, and ether ester compounds, specific examples of which are disclosed in Japanese Patent Publication No. 38826-1983.
No. 46-1592, and Special Publication No. 51-1'
Compounds disclosed as thickeners in US Pat. No. 1,272
good.

た、とえはポリエチレングリコール(MW6.0OO)
のジステアリルエーテル、ポリエチレングリコール(M
WaOOO)のジセチルエーテル、ポリエチレングリコ
ールの(MWIQOOO)ジステアリルエーテル、ポリ
エチレングリコール(MWi800)のセチルステアリ
ールエーテル、ポリエチレングリコール(MW5,00
0)のセチルノニルフェニルエーテル、ポリエチレング
リコール(MWaOoo)のステアリン酸ジエステル、
ポリエチレングリコール(MWaOoo)のバルミチン
酸ジエステル、ポリエチレングリコール(MWIQOO
O)のノニルフェノールステアリルエーテルエステル等
の化合物が挙げられる。
Toe is polyethylene glycol (MW6.0OO)
distearyl ether, polyethylene glycol (M
WaOOO) dicetyl ether, polyethylene glycol (MWIQOOO) distearyl ether, polyethylene glycol (MWi800) cetyl stearyl ether, polyethylene glycol (MW5,00)
0) cetyl nonylphenyl ether, stearic acid diester of polyethylene glycol (MWaOoo),
Valmitic acid diester of polyethylene glycol (MWaOoo), polyethylene glycol (MWIQOO)
Examples include compounds such as nonylphenol stearyl ether ester of O).

樹脂エマルションとしてはアクリル酸(エステル)、メ
タクリル酸(エステル)、酢酸ビニル等の重合した樹脂
エマルションや、活性水素化合物とポリイソシアネート
から得られるウレタンエマルション等が使用される。
As the resin emulsion, a polymerized resin emulsion of acrylic acid (ester), methacrylic acid (ester), vinyl acetate, etc., or a urethane emulsion obtained from an active hydrogen compound and polyisocyanate, etc. are used.

ウレタンエマルションの例としては、サンブレンUX−
2000(f、リエーテル型ウレタンエマルシコン、固
形分35%、三洋化成工業■製)、サンブレンUX−2
700(ポリエステlし型ウレタンエマルション、固形
分50%、三洋化成工業■製ン、サンブレンUX−35
00(ポリエーテル型ウレタンエマルション、固形分4
0%、三洋化成工業■製)等が挙げられる。
An example of a urethane emulsion is Sunbren UX-
2000 (f, riether type urethane emulsion, solid content 35%, manufactured by Sanyo Chemical Industries, Ltd.), Sunburen UX-2
700 (polyester type urethane emulsion, solid content 50%, manufactured by Sanyo Chemical Industries, Ltd., Sunbren UX-35
00 (polyether type urethane emulsion, solid content 4
0%, manufactured by Sanyo Chemical Industries, Ltd.).

本発明での一般式で示される化合物の添加量は樹脂エマ
ルシコンの処理浴中1〜o、oot%であり、好ましく
は0.8〜o、oos%、さらに好ましくは0.95〜
0.Olである。樹脂分に対しては0.01〜20%で
あり、好ましくは0.05〜15%、さらに好ましくは
01〜10%である。処理浴中1%以上添加すると処理
浴の粘度が高くなり、繊維製品に樹脂エマルションが含
浸しない欠点を生ずる処理浴の粘度は通常LOOOcp
s以下、好ましくは500cps以下、さらに好ましく
は100cps以下である。
The amount of the compound represented by the general formula in the present invention is 1 to 0.000%, preferably 0.8 to 0.00000%, more preferably 0.95 to 0.00000.000% in the resin emulsion treatment bath.
0. It is Ol. It is 0.01 to 20% with respect to the resin content, preferably 0.05 to 15%, and more preferably 01 to 10%. If it is added in excess of 1% to the treatment bath, the viscosity of the treatment bath increases, resulting in the disadvantage that the resin emulsion does not impregnate the textile product.The viscosity of the treatment bath is usually LOOOcp.
s or less, preferably 500 cps or less, more preferably 100 cps or less.

また本発明の化合物の添加方法は、先ず樹脂エマルショ
ンに加え水に希釈する方法、水に本発明の化合物を希釈
してから樹脂エマルションング、浸漬などで付与する方
法でもよく、特に限定されない。
The method of adding the compound of the present invention is not particularly limited, and may be a method in which the compound of the present invention is first added to a resin emulsion and diluted with water, or a method in which the compound of the present invention is diluted in water and then applied by resin emulsion, dipping, etc.

本発明の化合物のほかにさらに処理浴は柔軟剤、帯電防
止剤、撥水剤等の仕上剤や界面活性剤および染料、顔料
、またポバール、カルボキシメチルセルロース、メチル
セルロース、エチルセルロース、アルギン酸ソーダ等の
水溶性高分子を処理浴に加えることも出来る。
In addition to the compounds of the present invention, the treatment bath may also contain finishing agents such as softeners, antistatic agents, water repellents, surfactants, dyes, pigments, and water-soluble substances such as poval, carboxymethylcellulose, methylcellulose, ethylcellulose, and sodium alginate. Polymers can also be added to the treatment bath.

繊維製品には綿、レーヨン、ビニロン、ナイロン、アク
リル、ポリエステル等の天然繊維、化学繊維、合成繊維
の織布、編布、不織布等が使用出来る。
Textile products can include woven, knitted, and nonwoven fabrics made of natural fibers, chemical fibers, and synthetic fibers such as cotton, rayon, vinylon, nylon, acrylic, and polyester.

樹脂エマルションの処理条件は特に限定されないが、浸
漬処理の場合通常繊維製品(さマングルにて絞り率40
〜300%で絞られ乾燥機中60〜150℃の温度で乾
燥される。コート、スプレ一方法などで処理される場合
も、はぼ同程度の条件となるよう処理すればよい。
The treatment conditions for resin emulsion are not particularly limited, but in the case of dipping treatment, usually textile products (squeezing ratio 40 with a mangle) are used.
It is squeezed to ~300% and dried in a dryer at a temperature of 60-150°C. When processing by coating, spraying, etc., the processing may be performed under approximately the same conditions.

以下に実施例を挙げて説明するが、本発明は以下の実施
例に制約されるものではない。なお実施例中「部」とあ
るのは重量部を示す。
Examples will be described below, but the present invention is not limited to the following examples. In the examples, "parts" indicate parts by weight.

実施例1 サンブレンUX−3500(三洋化成工業■製ウレタン
エマルション)C40%固形分〕20部にポリエチレン
グリコール(MWaOOO)ジセチルエーテルの5%水
溶液を5部、水75部を加え均一に攪拌混合してエマル
ショ、ツ処理液を作成した。この処理液の中にポリエス
テル不織布を浸漬し、マングルにて絞った後(絞り率1
20%)、・100℃で10分間乾燥した。
Example 1 5 parts of a 5% aqueous solution of polyethylene glycol (MWaOOO) dicetyl ether and 75 parts of water were added to 20 parts of Sunbren UX-3500 (urethane emulsion manufactured by Sanyo Chemical Industries Ltd., C40% solids) and mixed by stirring uniformly. An emulsion and a treatment solution were prepared. After immersing a polyester nonwoven fabric in this treatment solution and squeezing it with a mangle (squeezing rate 1
20%), and dried at 100°C for 10 minutes.

比較−として同時にポリエチレン1グリコール(MW6
,000)ジセチルエーテルの無添加のものも同様に処
理した。結果は無添加のものは非常に硬く弾性が少なく
ペーパーライクの風合を有していたが、添加したものは
弾性およびボリュ゛ゞ  ・  。
As a comparison, polyethylene 1 glycol (MW6
, 000) without the addition of dicetyl ether was treated in the same manner. The results showed that the product without additives was very hard and had little elasticity and had a paper-like texture, but the product with additives was more elastic and voluminous.

一ム感の゛ある良好な風合を有していた。この風合の差
は、本発明の化合物を添加したものはエマルション粒子
の移行が生じておらず、均一に樹脂が付着しているが、
無添加のものは樹脂が移行しているためと考えられる。
It had a good texture with a uniform feel. This difference in texture is due to the fact that the emulsion particles do not migrate when the compound of the present invention is added, and the resin adheres uniformly.
This is thought to be due to the resin migrating in the case of additive-free products.

実施例2゜ サンブレンUX−2700(三洋化成工業■製ウレタン
エマルション)〔50%固形分〕10部に本発明の化合
物(表−CI)参照)の5%水溶液を5部、水を85部
加えて均一に攪拌混合してエマルション処理液を作成し
た。
Example 2 To 10 parts of Sunbren UX-2700 (urethane emulsion manufactured by Sanyo Chemical Industries, Ltd.) [50% solid content], 5 parts of a 5% aqueous solution of the compound of the present invention (see Table-CI)) and 85 parts of water were added. The emulsion treatment liquid was prepared by uniformly stirring and mixing.

この処理液の中にポリエステル不織布を浸漬しマングル
にて絞った後(絞り率100%入100℃で10分間乾
燥した。結果は表−(1)に記載のとおり。本発明の化
合物を添加したものはいづれも柔軟で弾性のある風合を
有しているが、無添加のものは風合が硬くペーパーライ
クのものであった。これは実施例1と同様にエマルショ
ン粒子が移行しているか否かの差と考えられる。
A polyester nonwoven fabric was immersed in this treatment solution and squeezed with a mangle (with a squeezing rate of 100% and dried at 100°C for 10 minutes.The results are shown in Table 1).The compound of the present invention was added. All of the samples had a soft and elastic texture, but the sample with no additives had a hard, paper-like texture.This may be due to migration of emulsion particles as in Example 1. It can be considered that the difference is whether or not.

表−0目 実施例3゜ 実施例2と同じ処理浴にポリエステルメリヤスを浸漬し
マングルにて絞った後(絞り率100%)、100℃で
10分間乾燥した。結果は実施例1.と同様に無添加の
ものは風合が硬くペーパーライクであったが、本発明の
化合物を添加したものはいづれもボリューム感のある柔
軟な風合を有していた。
Table - Item 0 Example 3 A polyester knitted fabric was immersed in the same treatment bath as in Example 2, squeezed with a mangle (squeezing ratio 100%), and then dried at 100°C for 10 minutes. The results are shown in Example 1. Similarly, those without additives had a hard and paper-like texture, but those containing the compound of the present invention all had a soft texture with a voluminous feel.

爬施例4゜ サンブレンUX−350020部、 5%ポリエチレン
クリコー・ル(MW6,000)ジセチルエーテル水溶
液5部、水75部からなるエマルション処理液に縦22
cm、横5国のポリエステル不織布を浸漬しマングルに
て絞り(絞り率120%)ただちに縦、横10(!I1
1の2枚のガラス板で中央部を挟み1−00℃で10分
乾燥させ、さらに2枚のガラス板を取り去り100℃で
10分乾燥させた不織布をウレタン樹脂に染色され易く
、ポリエステルには染色され難い合金染料(Kayak
alan Red BL日本化薬社製)の1%水溶液中
に10分間浸漬した後水洗して余分の染料を取り去った
。図−1は本発明の化合物を添加して処理した不織布で
、図−2は本発明の化合物を加えずに処理した不織布で
ある。図−1は均一に染色されているためウレタン樹脂
が均一に付着していることを示し、図−2の白い部分は
染色されていないのでウレタン樹脂が付着していないこ
とを示す。これはガラス板で挾んだ部分のエマルション
粒子が本発明の移行防止剤を用いない場合は水の蒸発と
ともに移行し、用いた場合はまったく移行しないことを
示して図面のi?I書(内容に変更なL) 昭和59年10月〉1日 1、事件の表示 昭和59年特許願第133533号 2、発明の名称 移行防止剤 3、補正をする者 事件との関係  特許出願人 1) 明細書第11員9〜12行の[4、図面の簡単な
説明」の欄を次のものに置換える。
Example 4 20 parts of Sunblen UX-3500, 5% polyethylene glycol (MW 6,000) dicetyl ether aqueous solution, 5 parts, and 75 parts of water were added vertically to an emulsion treatment solution for 22 hours.
cm, width 5mm polyester non-woven fabric is dipped and squeezed with a mangle (squeezing ratio 120%) immediately lengthwise and widthwise 10mm (!I1
The nonwoven fabric was sandwiched between two glass plates in step 1 and dried at 1-00℃ for 10 minutes, then the two glass plates were removed and dried at 100℃ for 10 minutes.The nonwoven fabric was easily dyed by urethane resin, and polyester Alloy dye that is difficult to dye (Kayak)
The sample was immersed in a 1% aqueous solution of Alan Red BL (manufactured by Nippon Kayaku Co., Ltd.) for 10 minutes, and then washed with water to remove excess dye. Figure 1 shows a nonwoven fabric treated with the addition of the compound of the present invention, and Figure 2 shows a nonwoven fabric treated without the addition of the compound of the invention. Figure 1 shows that the urethane resin is evenly adhered because it is uniformly dyed, and the white part of Figure 2 is not dyed, indicating that the urethane resin is not attached. This shows that the emulsion particles in the area sandwiched between the glass plates migrate with the evaporation of water when the migration inhibitor of the present invention is not used, but do not migrate at all when it is used. Book I (L with changes in content) October 1, 1980 1, Indication of the case 1982 Patent Application No. 133533 2, Invention title migration prevention agent 3, Relationship with the person making the amendment Patent application Person 1) Replace the column [4. Brief explanation of the drawings] in lines 9 to 12 of Part 11 of the specification with the following.

【図面の簡単な説明】[Brief explanation of the drawing]

図−1は本発明の防止剤を用いたエマルジョンで処理し
乾燥した繊維の形状を示す写真であり、図−2は防止剤
を用いないで処理した比較のための織縁の形状を示す写
真である。」 2) 明m書に添付した図面を次のものと置換える。
Figure 1 is a photograph showing the shape of a fiber treated with an emulsion using the inhibitor of the present invention and dried, and Figure 2 is a photograph showing the shape of a comparative weave edge treated without using an inhibitor. It is. 2) Replace the drawing attached to the statement of intent with the following.

Claims (1)

【特許請求の範囲】 1、下記一般式で示される化合物よりなる樹脂エマルシ
ョン移行防止剤。 一般式;XO−〔AO〕−_nY 〔ただしA;エチレン基またはこれを主体とする炭素数
2〜4個のアルキレン基、n; 50〜700、X、Y;RまたはR−CO、R;炭素数
7〜22の炭化水素基〕 2、樹脂エマルションがウレタンエマルションである特
許請求の範囲第1項記載の移行防止剤。
[Claims] 1. A resin emulsion migration inhibitor comprising a compound represented by the following general formula. General formula; Hydrocarbon group having 7 to 22 carbon atoms] 2. The migration inhibitor according to claim 1, wherein the resin emulsion is a urethane emulsion.
JP59133533A 1984-06-27 1984-06-27 Transfer inhibiting agent Pending JPS6112979A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP59133533A JPS6112979A (en) 1984-06-27 1984-06-27 Transfer inhibiting agent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP59133533A JPS6112979A (en) 1984-06-27 1984-06-27 Transfer inhibiting agent

Publications (1)

Publication Number Publication Date
JPS6112979A true JPS6112979A (en) 1986-01-21

Family

ID=15107027

Family Applications (1)

Application Number Title Priority Date Filing Date
JP59133533A Pending JPS6112979A (en) 1984-06-27 1984-06-27 Transfer inhibiting agent

Country Status (1)

Country Link
JP (1) JPS6112979A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0369651A (en) * 1989-08-10 1991-03-26 Nhk Spring Co Ltd Cushion body and production thereof
JPH0376854A (en) * 1989-08-10 1991-04-02 Nhk Spring Co Ltd Cushion material and its production

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0369651A (en) * 1989-08-10 1991-03-26 Nhk Spring Co Ltd Cushion body and production thereof
JPH0376854A (en) * 1989-08-10 1991-04-02 Nhk Spring Co Ltd Cushion material and its production

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