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JPS5933709B2 - Textile glue composition - Google Patents
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JPS5933709B2 - Textile glue composition - Google Patents

Textile glue composition

Info

Publication number
JPS5933709B2
JPS5933709B2 JP8388276A JP8388276A JPS5933709B2 JP S5933709 B2 JPS5933709 B2 JP S5933709B2 JP 8388276 A JP8388276 A JP 8388276A JP 8388276 A JP8388276 A JP 8388276A JP S5933709 B2 JPS5933709 B2 JP S5933709B2
Authority
JP
Japan
Prior art keywords
resin
vinyl acetate
viscosity
mol
sizing
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
Application number
JP8388276A
Other languages
Japanese (ja)
Other versions
JPS5310792A (en
Inventor
浩 床並
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.)
Mitsubishi Chemical Corp
Original Assignee
Nippon Synthetic Chemical Industry 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 Nippon Synthetic Chemical Industry Co Ltd filed Critical Nippon Synthetic Chemical Industry Co Ltd
Priority to JP8388276A priority Critical patent/JPS5933709B2/en
Publication of JPS5310792A publication Critical patent/JPS5310792A/en
Publication of JPS5933709B2 publication Critical patent/JPS5933709B2/en
Expired legal-status Critical Current

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Description

【発明の詳細な説明】 本発明はすぐれた糊剤性能を有する繊維糊剤組成物に関
するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a fiber sizing composition having excellent sizing properties.

従来経糸糊剤としては澱粉、ポリビニルアルコール、ア
クリル系ポリマー、酢酸ビニル−無水マレイン酸共重合
物、スチレン−無水マンイン酸共重合物などが知られて
いるが、ポリエステル、ナイロン、ポリプロピレン、ポ
リアクリロニトリル等の疎水性合成繊維に対する接着性
が不足して抱合力が不足したり、接着性を改善した組成
物では製織時の開口性が劣るという難点があった。
Conventional warp sizing agents include starch, polyvinyl alcohol, acrylic polymers, vinyl acetate-maleic anhydride copolymers, styrene-mannic anhydride copolymers, etc., but polyester, nylon, polypropylene, polyacrylonitrile, etc. However, compositions with improved adhesion properties have disadvantages in that they lack adhesion to hydrophobic synthetic fibers, resulting in insufficient binding power, and compositions with improved adhesion properties have poor opening properties during weaving.

しかして本出願人においては長年にわたる研究により、
マレイン酸モノアルキルエステル含量が01〜10モル
係で酢酸ビニル単位の60〜80モル係がケン化された
マレイン酸モノアルキルエステル−酢酸ビニル共重合体
部分ケン化物が疎水性合成繊維に対しても良好な接着力
を有し、吸湿性、粘着性が増大しないので抱合力がすぐ
れており、さらには製織時の開口性、糸切れの減少、糊
抜きの完全性などの点でも極めてすぐれていることを見
出していたが、現場試1験を長く続けた結果、大部分の
場合は伺らのトラブルも生じないものの、特にポリエス
テル加工糸について時折落糊量が無視できないケースが
あった。
However, through many years of research, the present applicant has found that
A partially saponified maleic acid monoalkyl ester-vinyl acetate copolymer with a maleic acid monoalkyl ester content of 01 to 10 moles and a saponified vinyl acetate unit of 60 to 80 moles is also suitable for hydrophobic synthetic fibers. It has good adhesive strength and does not increase hygroscopicity or stickiness, so it has excellent binding strength, and is also extremely excellent in terms of openness during weaving, reduced thread breakage, and complete desizing. However, as a result of a long series of on-site tests, we found that although in most cases the problems we encountered did not occur, there were occasional cases in which the amount of size removed could not be ignored, especially with processed polyester yarns.

落動通はポリエステル加工糸(J)加工条件、原糸油の
種類と付着量など諸条件の特殊な組合せにおいて発生す
るものと思われるが、いずれにせよどんな経歴の経糸を
用いてもトラブルの起きない繊維糊剤を開発することが
望ましいことは言うまでもない。
Dropping seems to occur due to a special combination of various conditions such as the polyester processed yarn (J) processing conditions, the type and amount of yarn oil attached, but in any case, no matter what history of warp yarn is used, the problem will not occur. It goes without saying that it is desirable to develop a fiber sizing agent that does not cause this phenomenon.

しかるに本発明者らはかかる課題を解決すべく鋭意研究
を重ねた結果、上記のマレイン酸モノアルキルエステル
−酢酸ビニル共重合体部分ケン化物の中から粘度の異な
るものを2種ブレンドするときは、経糸の種類、履歴を
問わす落動を有効ζこ防止しかつ接着性、抱合力、製織
性の点ですぐれた結果が得られることを見出し、本発明
を完成するに至った。
However, as a result of intensive research by the present inventors to solve this problem, we found that when blending two types of partially saponified maleic acid monoalkyl ester-vinyl acetate copolymer with different viscosities, The present invention was completed based on the discovery that it is possible to effectively prevent warp yarns from falling regardless of their warp type and history, and to obtain excellent results in terms of adhesion, binding force, and weavability.

即ち本発明の繊維糊剤組成物は、樹脂a及び樹脂すが共
ζこ マンイン酸モノアルキルエステル含量が0.1〜lOモ
ル係で酢酸ビニル単位の60〜80モル係がケン化され
たマレイン酸モノアルキルエステル−酢酸ビニル共重合
体ケン化物 であって、樹脂a及び樹脂すの温度50°Cにおける8
%水溶液の粘度(cps)ηa、ηb及びその比ηa/
ηbが ηa≧45 ηb≦30 ηa/ηb二15〜20 の関係を満たすような樹脂a及び樹脂すを重量で10〜
90:90〜10の比率で含有してなるものである。
That is, the fiber glue composition of the present invention has resin a and resin co-containing maleic acid monoalkyl ester content of 0.1 to 10 mol and 60 to 80 mol of vinyl acetate units saponified. A saponified acid monoalkyl ester-vinyl acetate copolymer, 8 at a temperature of 50°C of resin a and resin
% aqueous solution viscosity (cps) ηa, ηb and their ratio ηa/
Resin a and resin so that ηb satisfies the relationship ηa≧45 ηb≦30 ηa/ηb215-20 are 10 to 10% by weight
They are contained in a ratio of 90:90 to 10.

かかる樹脂a及び樹脂すの混合物を用いることにより樹
脂a単独或いは樹脂す単独の場合より一段とすぐれた落
動防止性が奏されるのである。
By using such a mixture of resin a and resin sinter, a much better anti-slip property can be achieved than when using resin a alone or resin sinter alone.

本発明におけるマレイン酸モノアルキルエステル−酢酸
ビニル共重合体部分ケン化物のマレイン酸モノアルキル
エステル成分としては、マレイン酸モノメチル、マレイ
ン酸モノエチル、マレイン酸モノプロピル、マレイン酸
モノブチルなどがあげられる。
Examples of the monoalkyl maleate component of the partially saponified monoalkyl maleate-vinyl acetate copolymer in the present invention include monomethyl maleate, monoethyl maleate, monopropyl maleate, and monobutyl maleate.

そして重合体中のマレイン酸モノアルキルエステルの含
量は0.1〜10モル係の範囲にあることが必要であり
、その含量が0.1モル係未満のときは疎水性合成繊維
に対する接着性や抱合性が不足し、一方その含量が1.
0モル係を越えるときは吸湿性、粘着性が増大し、抱合
性が低下する。
The content of maleic acid monoalkyl ester in the polymer needs to be in the range of 0.1 to 10 mol, and when the content is less than 0.1 mol, the adhesion to hydrophobic synthetic fibers The conjugation property is insufficient, while the content is 1.
When the molar ratio exceeds 0, hygroscopicity and stickiness increase, and conjugation property decreases.

マレイン酸モノアルキルエステル以外の他の不B′1和
カルボン酸、たとえばアクリル酸、メタクリル酸、クロ
トン酸など或いはこれらのアルキルエステルと酢酸ビニ
ルとの共重合体の部分ケン化物は糊付としての性質がマ
レイン酸モノアルキルエステルを共重合成分とした場合
に到底及ばない。
Other non-B' monoalkyl carboxylic acids other than maleic acid monoalkyl esters, such as acrylic acid, methacrylic acid, crotonic acid, etc., or partially saponified products of copolymers of these alkyl esters and vinyl acetate have properties as adhesives. is far below that obtained when maleic acid monoalkyl ester is used as a copolymerization component.

もつともマレイン酸ジアルキルエステル、無水マレイン
酸、フリーのマレフィン酸を共重合モノマーとして用い
たときは、酢酸ビニルとの共重合やケン化をアルコール
中で行なうことにより最終的にモノアルキルエステルの
形に変換していれば本発明の範囲に含まれる。
Of course, when maleic acid dialkyl ester, maleic anhydride, or free malefinic acid is used as a copolymerization monomer, it is finally converted into a monoalkyl ester form by copolymerization with vinyl acetate or saponification in alcohol. If so, it is within the scope of the present invention.

重合体中の酢酸ビニル単位のTン化度は60〜80モル
係の範囲に調節すべきであり、ケン化度がこの範囲より
小さいときは糊抜性が劣り、この範囲より太きいときは
繊維に対する接着性が劣る。
The degree of T-tonation of vinyl acetate units in the polymer should be adjusted to a range of 60 to 80 moles; if the degree of saponification is smaller than this range, desizing properties will be poor; if it is thicker than this range, Poor adhesion to fibers.

なおケン化は通常アルカリ触媒で行なうので、重合体中
のマレイン酸モノアルキルエステル単位は(ただしRは
アルキル基、Mはナトリウム、カリウムなどのアルカリ
金属又はNH4)の如<(1)かう(2)の形へ変換し
ているのが普通であるが、本発明においては(1)又は
(2)のいずれの態様であってもよい。
Since saponification is usually carried out using an alkali catalyst, the maleic acid monoalkyl ester unit in the polymer has the following formula (where R is an alkyl group and M is an alkali metal such as sodium or potassium or NH4) < (1) such (2 ), but in the present invention, either embodiment (1) or (2) may be used.

上記の如き組成を有するマレイン酸モノアルキルエステ
ル−酢酸ビニル共重合体部分ケン化物であってもその重
合度、分枝の程度によってはその水溶液粘度の異なるも
のが得られる。
Even if a partially saponified maleic acid monoalkyl ester-vinyl acetate copolymer having the above-mentioned composition can be obtained, the aqueous solution viscosity will differ depending on the degree of polymerization and degree of branching.

本発明においては上記組成の樹脂中から選ばれた樹脂a
及び樹脂すであって、その温度50℃における8%水溶
液の粘度(cps)ηa、ηb及びその比ηa/ηbが ηa≧45 ηb≦30 ηa/ηb=1゜5〜20 の関係を満たすような樹脂が用いられる。
In the present invention, a resin a selected from resins having the above composition is used.
and resin, such that the viscosity (cps) ηa, ηb and the ratio ηa/ηb of an 8% aqueous solution at a temperature of 50°C satisfy the following relationships: ηa≧45 ηb≦30 ηa/ηb=1°5-20 resin is used.

樹脂aは高粘度のものであり、その温度50℃における
8%水溶液の粘度ηaが45cps以上であることが必
要であって、45cps未溝のものでは低粘度サイドの
樹脂すと混ぜても相乗効果は期待しえない。
Resin a has a high viscosity, and the viscosity ηa of its 8% aqueous solution at a temperature of 50°C must be 45 cps or more, and if it is ungrooved at 45 cps, it will not synergize even when mixed with a lower viscosity resin. The effect cannot be expected.

なお特に好ましい範囲は50〜300cps であり、
余りに高粘度のものは糊付の円滑性の面で制約を受ける
Note that a particularly preferable range is 50 to 300 cps,
If the viscosity is too high, there will be restrictions on the smoothness of gluing.

一方樹脂すは低粘度のものであり、その温度50℃にお
ける8%水溶液の粘度ηbが30cps以下であること
が必要であって、30cpsを越えるときは高粘度サイ
ドの樹脂aと混合しても相乗効果は期待しえない。
On the other hand, the resin has a low viscosity, and the viscosity ηb of an 8% aqueous solution at a temperature of 50°C must be 30 cps or less, and if it exceeds 30 cps, it can be mixed with the higher viscosity resin Synergistic effects cannot be expected.

なお特に好ましい範囲は5〜25cpsであり、余りに
低粘度のものは抱合性や落動量の面で制約を受ける。
Note that a particularly preferable range is 5 to 25 cps, and if the viscosity is too low, there will be restrictions in terms of conjugation ability and amount of falling motion.

又樹脂aの粘度ηaと樹脂すの粘度ηbは前記の如き範
囲にあるだけでなく、その比ηa/ηbが1.5〜20
の範囲にあることが要求される。
In addition, the viscosity ηa of resin a and the viscosity ηb of resin a are not only within the above range, but also have a ratio ηa/ηb of 1.5 to 20.
is required to be within the range of

ηa/ηbが15未満のとき、即ちηaとηbとが接近
しすぎているときは樹脂a単独使用又は樹脂す単独使用
の場合と大差のない効果が得られるにすぎず、一方ηa
/ηbが20を越えるとき、即ち粘度Oこ極端に差があ
るときは糊付の円滑性が損なわれる傾向が見られる。
When ηa/ηb is less than 15, that is, when ηa and ηb are too close to each other, the same effect as when using resin a alone or resin s alone can be obtained; on the other hand, when ηa
When /ηb exceeds 20, that is, when there is an extreme difference in viscosity O, the smoothness of gluing tends to be impaired.

次に樹脂aと樹脂すとは重量で10〜90:90〜10
の比率で使用され、この範囲以外のときにはそれぞれ単
独使用の場合と余り変わらない糊剤性能しか得られない
Next, resin a and resin soot are 10 to 90:90 to 10 by weight.
When the ratio is outside this range, the performance of the glue is not much different from that when each is used alone.

以上述べた樹脂a及び樹脂すは水に溶解して糊液が調製
される。
A paste solution is prepared by dissolving the resin a and the resin solution described above in water.

糊液中の樹脂分濃度は約3.5〜11重量係の範囲に設
定するのが通常である。
The resin content concentration in the size liquid is usually set in a range of about 3.5 to 11 parts by weight.

なお糊液中には消泡剤、各種油剤など公知の添加剤が必
要に応じ添加される。
Note that known additives such as antifoaming agents and various oils may be added to the size liquid as necessary.

本発明の糊剤組成物はフイラメン[・糸、ウーリー加工
糸、紡績糸などの経糸の糊付に供されるが、経糸の種類
、原糸油の付着状況を問わす落動が有効に防止されるの
で本業界に貢献するところが大きい。
The sizing composition of the present invention is used for sizing the warp yarns of filament yarn, woolly processed yarn, spun yarn, etc., but it effectively prevents falling, regardless of the type of warp yarn or the adhesion status of raw yarn oil. This will greatly contribute to the industry.

次に例をあげて本発明の組成物をさらに説明する。Next, the composition of the present invention will be further explained by giving examples.

以下1%」とあるのは特にことわりのない限り重量係を
示すものとする。
1% or less" indicates the weight ratio unless otherwise specified.

例1 次の組成の糊剤組成物を用いて各社のポリエステル加工
糸8品種の糊付、製織、糊抜を行なった。
Example 1 Sizing, weaving, and desizing of eight types of polyester processed yarns from various companies were carried out using a sizing composition having the following composition.

結果を第1表に示す。The results are shown in Table 1.

樹脂a マレイン酸モノメチル含量が0.7モル係で酢酸ビニル
単位の70.3モル係がケン化されたマレイン酸モノメ
チル−酢酸ビニル共重合体部分ケン化物 50℃における8%水溶液の粘 ()3o。
Resin a Partially saponified monomethyl maleate-vinyl acetate copolymer with a monomethyl maleate content of 0.7 mol and vinyl acetate units of 70.3 mol. Viscosity of an 8% aqueous solution at 50°C () 3o .

度ηa二60cpsのもの 樹脂b マレイン酸モノメチル含量が0.4モル係で酢酸ビニル
単位の69,5モル係がケン化されたマレイン酸モノメ
チル−酢酸ビニル共重合体部分ケン化物 0℃における8%水溶液の粘 (” ) 5.5% 度ηb=9.8cpsのもの 油剤 0.3% 平滑剤 0.2係水
残り (ηa/ηb=6.1となる。
Partially saponified monomethyl maleate-vinyl acetate copolymer with a monomethyl maleate content of 0.4 mol and a vinyl acetate unit of 69.5 mol. 8% at 0°C Viscosity of aqueous solution ('') 5.5% Degree ηb = 9.8 cps Oil agent 0.3% Smoothing agent 0.2 Water retention
The remainder (ηa/ηb=6.1).

)糊付条件 対象糸 ポリエステルウーリー加工糸 (75デニール/36フライメント、 無撚) 糊付機 津田駒社製KS−J型ワーピングスラツシャ
ー 糊付条件 枠立数 1050本 絞り全荷重 180〜260ゆ 糊液温度 50℃ 乾燥温度 チャンバー 120’CX 2シリンダー
100℃×2 巻取速度 95m/min サイジングトラフト 1.2% 糊付量 9〜lo係 製織条件 織物は5枚朱子で、総経糸本数8400本、織上中37
5吋、緯糸密度107本/吋。
) Yarn subject to sizing conditions Polyester woolly processed yarn (75 denier/36 flyment, non-twisted) Sizing machine Tsudakoma KS-J type warping slatsher Sizing conditions Number of frames 1050 drawings Full load 180-260 Sizing liquid temperature: 50℃ Drying temperature: Chamber: 120'C Book, Orijo Junior High School 37
5 inches, weft density 107 threads/inch.

織機は自動織機i6orpmで、50mを1疋として4
0疋を製織した。
The loom is an automatic loom i6orpm, with 50m as one thread.
Weaved 0 stitches.

糊抜条件 2 g/lの炭酸ソーダ及び2g/lの洗剤(第一工業
製薬社製モノゲン)を含有する精練液中で浴比1/30
〜1150、温度90〜95℃で30〜60分間処理し
た後水洗。
Descaling conditions 2 Bath ratio 1/30 in a scouring solution containing g/l of soda carbonate and 2 g/l of detergent (Monogen, manufactured by Daiichi Kogyo Seiyaku Co., Ltd.)
~1150℃, treated at a temperature of 90-95°C for 30-60 minutes, and then washed with water.

対照例 1 樹脂aを5,7%用い、樹脂すの使用を省略したほかは
例1と同様にして糊液を調製し、以下糊付、製織を行な
った場合。
Comparative Example 1 A size solution was prepared in the same manner as in Example 1 except that 5.7% of resin a was used and the use of resin was omitted, and the following sizing and weaving were performed.

対照例 2 樹脂すを10.5%用い、樹脂aの使用を省略したほか
は例1と同様にして糊液を調製し、以下糊付、製織を行
なった場合。
Comparative Example 2 A size solution was prepared in the same manner as in Example 1 except that 10.5% of resin A was used and resin a was omitted, and the following sizing and weaving were performed.

対照例 3 従来公知のテトロン用糊剤(重合度500、ケン化度8
8モル係のポリビニルアルコールとアクリル酸エチル−
メタクリル酸メチル−メタクリル酸(50:35:15
重量比)共重合体のソーダ塩とを重量で5:5の割合に
混合し、さらに油剤を含む糊液)を使用したほかは例1
と同様にして糊付、製織を行なった場合。
Comparative Example 3 Conventionally known sizing agent for Tetron (polymerization degree 500, saponification degree 8)
8 molar polyvinyl alcohol and ethyl acrylate
Methyl methacrylate-methacrylic acid (50:35:15
Example 1 except that the copolymer soda salt (weight ratio) was mixed at a ratio of 5:5 by weight, and a glue containing an oil agent was used.
When pasting and weaving are carried out in the same manner as above.

第1表からも明らかなように本発明の糊剤組成物を使用
した場合にはポリエステル加工糸の種類の如何を問わず
極めて良好な結果が得られる。
As is clear from Table 1, when the size composition of the present invention is used, extremely good results can be obtained regardless of the type of polyester processed yarn.

このことは経糸の品種に合わせてその都度糊液組成を変
更する必要がないことを意味し、実用性が極めて犬であ
ることを示す。
This means that there is no need to change the size liquid composition each time depending on the type of warp, and shows that it is extremely practical.

例2 樹脂aとしてマレイン酸モノメチル含量が05モル係で
酢酸ビニル単位の69.5モル係がケン化されたマレイ
ン酸モノメチル−酢酸ビニル共重合体部分ケン化物(5
0°Cにおける8%水溶液の粘度ηaニア 0 cps
のもの)を4.2%、樹脂すとしてマンイン酸モノメチ
ル含量が0.5 モル%テ酢eビニル単位の71.4モ
ル係がケン化されたマレイン酸モノメチル−酢酸ビニル
共重合体部分ケン化物(50℃における8係水溶液の粘
度ηb = 10.3cpsのもの)を4.2%用いた
ほかは例1と同様にして糊液を調製し、以下糊付、製織
を行なった。
Example 2 Resin a is a partially saponified monomethyl maleate-vinyl acetate copolymer with a monomethyl maleate content of 0.5 mol and a vinyl acetate unit of 69.5 mol.
Viscosity of 8% aqueous solution at 0°C ηa Near 0 cps
Partially saponified product of monomethyl maleate-vinyl acetate copolymer in which 4.2% of monomethyl manate (based on resin) and 71.4 moles of vinyl units are saponified. A size solution was prepared in the same manner as in Example 1 except that 4.2% of 8% aqueous solution (viscosity ηb = 10.3 cps at 50° C.) was used, and then sizing and weaving were performed.

なおηa/ηb二6.8となる。Note that ηa/ηb2 is 6.8.

例3 樹脂aとしてマレイン酸モノイソブチル含量が0.7モ
ル係で酢酸ビニル単位の72.0モル係がケア化された
マレイン酸モノイソブチル−酢酸ビニル共重合体部分ケ
ン化物(50℃における8%水溶液の粘度ηa二62
cpsのもの)を4.2%、樹脂すとしてマレイン酸モ
ノメチル含量が0.5モル係で酢酸ビニル単位の71.
4モル係がケン化されたマレイン酸モノメチル−酢酸ビ
ニル共重合体部分ケン化物(50°Cにおける8%水溶
液の粘度ηb= 10.3 cpsのもの)を4.2係
用いたほかは例1と同様にして糊液を調製し、以下糊付
、製織を行なった。
Example 3 Partially saponified monoisobutyl maleate-vinyl acetate copolymer with a monoisobutyl maleate content of 0.7 mol and 72.0 mol of vinyl acetate units as resin a (8% at 50°C) Viscosity of aqueous solution ηa262
cps) is 4.2%, the monomethyl maleate content is 0.5 mol, and the vinyl acetate unit is 71.
Example 1 except that a partially saponified monomethyl maleate-vinyl acetate copolymer (viscosity of an 8% aqueous solution at 50°C, ηb = 10.3 cps) was used in Example 1. A size solution was prepared in the same manner as above, and the following steps were performed: pasting and weaving.

なおηa/ηb = 6.0となる。結果を第2表に示
す。
Note that ηa/ηb = 6.0. The results are shown in Table 2.

Claims (1)

【特許請求の範囲】 1 樹脂a及び樹脂すが共ζこ マレイン酸モノアルキルエステル含量が01〜1.0モ
ル係で酢酸ビニル単位の60〜80モル係がケン化され
たマレイン酸モノアルキルエステル−酢酸ビニル共重合
体部分ケン化物であって、樹脂a及び樹脂すの温度50
°Cにおける8係水溶液の粘度(eps)ηa、ηb及
びその比ηa/ηbが ηa≧45 ηb≦30 ηa/ηb=15〜20 の関係を満たすような樹脂a及び樹脂すを重量で10〜
90:90:10の比率で含有してなる繊維糊剤組成物
。 2 マレイン酸モノアルキルエステルがマレイン酸モノ
メチルである特許請求の範囲1記載の組成物。
[Scope of Claims] 1. Resin a and resin sugamo ζ Maleic acid monoalkyl ester having a content of 01 to 1.0 mol and in which 60 to 80 mol of vinyl acetate units have been saponified. - Partially saponified vinyl acetate copolymer, the temperature of resin a and resin 50
Resin a and resin so that the viscosity (eps) ηa, ηb and the ratio ηa/ηb of an aqueous solution at °C satisfy the following relationships: ηa≧45 ηb≦30 ηa/ηb=15-20 by weight 10~
A fiber glue composition containing the fiber paste composition in a ratio of 90:90:10. 2. The composition according to claim 1, wherein the maleic acid monoalkyl ester is monomethyl maleate.
JP8388276A 1976-07-13 1976-07-13 Textile glue composition Expired JPS5933709B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP8388276A JPS5933709B2 (en) 1976-07-13 1976-07-13 Textile glue composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP8388276A JPS5933709B2 (en) 1976-07-13 1976-07-13 Textile glue composition

Publications (2)

Publication Number Publication Date
JPS5310792A JPS5310792A (en) 1978-01-31
JPS5933709B2 true JPS5933709B2 (en) 1984-08-17

Family

ID=13815017

Family Applications (1)

Application Number Title Priority Date Filing Date
JP8388276A Expired JPS5933709B2 (en) 1976-07-13 1976-07-13 Textile glue composition

Country Status (1)

Country Link
JP (1) JPS5933709B2 (en)

Also Published As

Publication number Publication date
JPS5310792A (en) 1978-01-31

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