JPS6249391B2 - - Google Patents
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- JPS6249391B2 JPS6249391B2 JP8985682A JP8985682A JPS6249391B2 JP S6249391 B2 JPS6249391 B2 JP S6249391B2 JP 8985682 A JP8985682 A JP 8985682A JP 8985682 A JP8985682 A JP 8985682A JP S6249391 B2 JPS6249391 B2 JP S6249391B2
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- carbon atoms
- sewing
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Description
本発明はポリエステルマルチフイラメント糸を
用いた畳へり用縫着糸(以下、縫着糸という)に
対する処理剤に関するものである。
従来は畳床に畳べりを縫い付ける場合に畳職人
が手で縫い付けていたが、近年は自動的に縫い付
けが出来るミシンに似た縫着機が開発されて殆ど
この機械を使用する様になつた。
縫着機を使用する事によりスピードアツプ及び
縫目の均一化等は実現したが、反面縫着機で部厚
い畳床を締め付けながら縫い付けるとき間歇的で
はあるが非常に強い衝撃力が加わるため縫着糸の
切断という致命的障害をひき起す問題が発生し
た。
この衝撃力に耐え得る様、縫着糸を太くすると
ともに縫着糸表面に鉱物油、パラフイン、シリコ
ーンオイル等の平滑剤を処理して縫着糸と縫針及
び縫着糸と畳床材との摩擦力を低下させて衝撃力
を緩和する方法がとられているが、糸を太くする
ことは経済的に限度が有り又平滑剤量が多いと高
湿時等では平滑性を阻害する結果となり未だ満足
すべき方法にまで到つていない。
一方、畳床は非常に部厚く弾性に富んではいる
が、瞬間的な反撥弾性はもつていない。従つて縫
着糸で締め付けながら縫い付けた後徐々に締め付
けが弛み框を波打たせる結果となり、畳の商品価
値を著しく低下させる。これは畳床のもつ本質的
な瞬間圧縮復元力の弱さにも起因するが、縫着糸
の伸度の大きさにも影響される。そこで縫着糸の
伸度を低くする目的で熱可塑性樹脂を縫着糸に含
浸させて繊維−繊維間を接着させて目的を達する
技術が提案され実行されている。しかしながら熱
可塑性樹脂によつて繊維−繊維間の接着を強固に
するほど縫着機による衝撃力に対する接着糸の抵
抗力(応力緩和性)が低下する。この相反する性
能に適度にバランスをとつて縫着糸を処理してい
るのが現状であるが、糸切れ、目落ち、糸のほつ
れ等の問題はいぜんとして残つており、益々合理
化され高速化する縫製技術に対応していくには必
ずしも満足すべきものではなく、より一層優れた
平滑性を付与し得る処理剤の開発が要請されてい
る。
本発明者等はポリエステル繊維縫着糸の性能
を、仕上工程で付与せしめる処理剤によつて大幅
に向上せしめるべく処理剤について鋭意研究した
結果、
(1) 縫着糸の縫着能を大幅に向上せしめるには、
金属に対する高接圧時の摩擦力を低下せしめる
のみでなく、低接圧(低速)時の摩擦力も低下
させる必要があり、速度依存性を小さくするこ
と、
(2) 縫着機による間歇的な強い衝撃力を緩和する
には、熱可塑性樹脂によつて繊維−繊維間を接
着させる従来公知の方法は効果がなく、繊維−
繊維間の摩擦力を低下させ、且つ静摩擦係数と
動摩擦係数を近似させるほど有効であること。
(3) 高接圧で擦過された後の縫着糸の剛性が擦過
前より高くなるほど縫着時のループ形成性が良
好となり目落ち等の欠陥が発生し難く又縫着糸
の伸度低減にも有効であることおよび
(4) 結晶パラフイン及び/又は天然ワツクス或は
合成ワツクス、ポリオキシアルキレンアルキル
アミン、脂肪酸とポリアルキレンポリアミンと
のアマイド化合物の第4級アンモニウム塩、非
イオン系界面活性剤を併用すると対金属高接圧
摩擦力、対金属低接圧摩擦力とも大幅に低下
し、繊維−繊維間の静摩擦係数、動摩擦係数が
近似した低下性を示し且つ縫着糸擦過後の剛性
を高めることが出来る
との知見を得、本発明を完成するに到つた。
即ち、本発明は結晶パラフイン及び/又は天然
ワツクス或は合成ワツクス、ポリオキシアルキレ
ンアルキルアミン、脂肪酸とポリアルキレンポリ
アミンとのアマイド化合物の第4級アンモニウム
塩、非イオン系界面活性剤を配合して乳化分散す
ることを特徴とするポリエステル繊維製畳へり縫
着糸用処理剤である。
本発明で使用する結晶パラフイン及び/又は天
然あるいは合成ワツクスは変性ワツクス或は合成
エステル型ワツクスを含む。高接圧時結晶パラフ
イン及び各種ワツクス類は融点が50〜90℃のもの
が好ましい。融点が50℃以下になると高接圧時の
油膜強度が不足し油膜切れが発生する。特に衝撃
力が加わつた場合は縫着糸の融断を引き起す。
融点が90℃以上になると溶融時の粘度が高くな
り粘着力の発生により摩擦力は逆に高くなる傾向
を示す。
具体例としては直鎖結晶性パラフイン、酸化パ
ラフインミクロクリスタルワツクス、酸化ミクロ
クリスタルワツクス、カルナバワツクス、合成エ
ステル型ワツクス等を挙げることができる。
本発明で使用するポリオキシアルキレンアルキ
ルアミンは一般式
〔式中R1は炭素数12〜22の直鎖アルキル基を
示し、R2,R3は炭素数2〜3のアルキレン基を
示し、2≦m+n≦10である。〕で表わされる化
合物である。
式〔1〕のR1は炭素数12〜22の範囲のものが
使用出来るが特に18〜22の範囲のものが好まし
い。炭素数が12より小さいと潤滑剤の平滑特性を
阻害するとともに高温時における潤滑剤溶媒の蒸
発が減しくなる。一方炭素数が22より大きくなる
と高温溶融時の粘度が高くなり粘着力により摩擦
力を高くする。
式〔1〕中のR2,R3は炭素数2〜3のアルキ
レン基であるが同一であつても異なつていても良
い。
オキシアルキレン鎖m+nが11以上になると潤
滑性能を低下させるとともに潤滑剤との相溶性が
悪くなり油膜強度向上効果が著しく低下する。
本発明で使用する脂肪酸とポリアルキレンポリ
アミンとのアマイド化合物の第4級アンモニウム
塩において使用する脂肪酸は炭素数11〜21のもの
が好ましいが特に炭素数17〜21の脂肪酸が好まし
い。炭素数が11より小さい場合は摩擦力低下能力
が劣り、炭素数が21よりも大きくなつた場合は溶
融時の粘着力が増加し摩擦力を高くする欠点が出
る。
ポリアルキレンポリアミンとして使用されるも
の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、ペンタエチレ
ンヘキサミン等が挙げられる。
本発明で使用される非イオン系界面活性剤は非
イオン系であればよく特に限定する必要はない
が、通常油性物質を乳化するのに用いられるエス
テル型非イオン系界面活性剤、エーテル型非イオ
ン系界面活性剤の1種又は2種以上の使用する。
本発明の処理剤の組成比は例えば固型分100重
量部に対し各種ワツクス70〜90重量部、ポリオキ
シアルキレンアルキルアミン2〜10重量部、脂肪
酸とポリアルキレンポリアミンとのアマイド化合
物の第4級アンモニウム塩2〜10重量部、非イオ
ン系界面活性剤10〜25重量部などの範囲を用いる
ことができる。
各種ワツクスが70重量部未満のときは平滑性が
不足して糸切れの原因となる。又90重量部を越え
ると水中での乳化が困難となり乳化安定性が著し
く悪化し使用に耐えなくなる。
ポリオキシアルキレンアルキルアミンが2重量
部未満になると高接圧時に潤滑剤の油膜切れが発
生し糸切れの原因となる。又10重量部を越えると
平滑性が低下し正常な縫着が不能となる。
第4級アンモニウム塩が2重量部未満では平滑
性の糸速度依存性が高くなりステイツクスリツプ
等の異状張力が加わつた時糸切れを誘発させる。
又繊維−繊維間の摩擦力が高くなり衝撃力に抗し
得なくなる。10重量部を越えると高接圧時の摩擦
力が著しく高くなり糸切れの原因となる。
乳化剤として使用する非イオン系界面活性剤は
吸湿すると平滑性が低下するので可能な限り少量
にする事が望ましいが、乳化安定性の面から縫着
糸加工工程上支障を来たさないだけの量は使用す
る必要がある。
本発明の処理剤は通常エマルジヨンの状態で用
いられ、2〜10重量%エマルジヨン濃度で用いる
のが最適である。
本発明の処理剤は優れた縫着性能を得るため縫
着糸に対して1.0〜10.0重量%、好ましくは2.0〜
5.0重量%付着させるとワツクス、ポリオキシア
ルキレンアルキルアミン、第4級アンモニウム塩
3者の相剰効果で縫着機に適合した優れた縫着性
を有する縫着糸を得る事が出来る。
本発明の処理剤はエマルジヨンにして縫着糸に
付着させるが、縫着糸は通常トータルデニール
3000de以上と非常に太いものが多く、又処理剤
付与後高緊張下で160〜200℃の熱セツトを行なう
必要があるので処理剤付与方法は浸漬法が好まし
い。
以下実施例によつて具体的に例示する。
なお、平滑性、剛性、擦過後の剛性保持率は以
下の方法により測定した。
また実施例、比較例における処理剤の組成比の
単位は特に断らない限り重量部であり、%は重量
%を表わす。
〔平滑性〕
インストロン型引張強度試験機を用いロードセ
ル側に畳針1本を固定させ、針穴を通して5Kgの
荷重を掛けた縫着糸を180゜接触させて20mm/
minの速度で引張つた時の張力で表わす。
〔剛性〕
上野山機工製フーアイメーターを使用し10mm間
隙への挿入荷重を剛性として表わす。
〔擦過後の剛性保持率〕
300gの張力を掛けた縫着糸をS字型コンペン
セーター2個及びテンシヨンコントローラー(7
本バー)1個を糸速30m/minで通過させた後剛
性を測定し下記式により剛性保持率を算出する。
擦過後の剛性(g)/擦過前の剛性(g)×100=剛
性保持率(%)
実施例 1〜6
1000デニールのポリエチレンテレフタレートフ
イラメント高強力糸250フイラメントを3本合糸
して撚糸を行なつた。
縫着糸に第1表に示す処理剤をエマルジヨンで
浸漬法により付与せしめ100℃で10分間、熱風乾
燥を行なつた後高張力での緊張のもとに200℃で
30秒間熱セツトを行なつた。
かくして得られた縫着糸の平滑性、剛性、擦過
後の剛性保持率を測定した。又縫着機による実機
テストも実施して第1表に示した効果が得られ
た。
比較例 1〜6
第1表に示すように本発明の処理剤の構成成分
のいずれかを含まない処理剤あるいは処理剤組成
の重量比が本発明の範囲外である場合などについ
て実施例1〜6と同様に実験し評価結果を第1表
に示した。
縫着機によるテスト結果における糸切れ数、目
落ち数は以下のごとく肉眼観察により数えた。
(1) 平縫、返し縫の場合
畳10枚に平縫および返し縫を施したときの縫
着機の水切れ回数が糸切れ数であり平縫の両側
面、それら両側面の返し縫があるので(畳)10
(枚)×(平縫)2(回)×(返し縫)2(回)=
(計)40回の縫着機による縫着を行なつたとき
の糸切れ数(ケ)である。またそのときの上糸
と下糸のからみが円滑にいかず目落ちを生じた
ときの目落ちの数を肉眼検査で数えたのが目落
ち数(ケ)である。
(2) 框縫の場合
この場合も畳10枚についての評価結果である
が、返しがないのでこの場合は10×2=20回縫
着を行なつたときの結果となる。
The present invention relates to a treatment agent for sewing thread for tatami edges (hereinafter referred to as sewing thread) using polyester multifilament thread. Traditionally, tatami craftsmen used to sew tatami edges on tatami floors by hand, but in recent years, sewing machines similar to sewing machines that can sew automatically have been developed, and most people now use these machines. It became. By using a sewing machine, we were able to increase speed and make the stitches more uniform, but on the other hand, when sewing a thick tatami floor while tightening it, a very strong impact force is applied intermittently. A fatal problem occurred in which the suture thread broke. In order to withstand this impact force, the sewing thread is made thicker and the surface of the sewing thread is treated with a smoothing agent such as mineral oil, paraffin, silicone oil, etc., so that the sewing thread and the sewing needle and the sewing thread and the tatami flooring material are separated. Methods have been taken to reduce the frictional force and alleviate the impact force, but there is an economic limit to making the thread thicker, and if the amount of smoothing agent is too large, the smoothness will be impaired in times of high humidity. I have not yet arrived at a method that satisfies me. On the other hand, although tatami flooring is extremely thick and highly elastic, it does not have instantaneous rebound properties. Therefore, after sewing while tightening with sewing thread, the tightening gradually loosens, causing the stile to wave, which significantly reduces the commercial value of the tatami. This is due to the inherent weakness of the instantaneous compression recovery force of the tatami floor, but it is also affected by the degree of elongation of the sewing thread. Therefore, in order to reduce the elongation of the sewing thread, a technique has been proposed and implemented in which the sewing thread is impregnated with a thermoplastic resin to bond the fibers together. However, as the bond between fibers is strengthened by the thermoplastic resin, the resistance (stress relaxation property) of the adhesive thread to the impact force exerted by the sewing machine decreases. Currently, sewing threads are processed by appropriately balancing these conflicting performances, but problems such as thread breakage, dropped stitches, and frayed threads still remain, so it is becoming more and more streamlined and faster. This is not necessarily satisfactory in keeping with the sewing technology, and there is a need for the development of a processing agent that can impart even better smoothness. The inventors of the present invention have conducted intensive research on processing agents in order to significantly improve the performance of polyester fiber sewing threads by applying them during the finishing process. To improve,
It is necessary not only to reduce the frictional force when the contact pressure is high against metal, but also to reduce the frictional force when the contact pressure is low (low speed), and to reduce the speed dependence. To alleviate strong impact forces, the conventional method of bonding fibers together using thermoplastic resin is ineffective;
It should be effective enough to reduce the frictional force between fibers and approximate the coefficient of static friction and the coefficient of kinetic friction. (3) The higher the stiffness of the sewing thread after rubbing with high contact pressure than before rubbing, the better the loop formation properties during sewing, the less defects such as dropped stitches will occur, and the elongation of the sewing thread will be reduced. and (4) crystalline paraffin and/or natural wax or synthetic wax, polyoxyalkylene alkylamine, quaternary ammonium salt of amide compound of fatty acid and polyalkylene polyamine, nonionic surfactant. When used in combination, both the high contact pressure friction force against metal and the low contact pressure friction force against metal are significantly reduced, and the static friction coefficient and dynamic friction coefficient between fibers show similar decreases, and the stiffness after rubbing of the sewing thread decreases. The present invention was completed based on the knowledge that it is possible to improve the performance. That is, the present invention emulsifies crystalline paraffin and/or natural wax or synthetic wax, polyoxyalkylene alkylamine, a quaternary ammonium salt of an amide compound of fatty acid and polyalkylene polyamine, and a nonionic surfactant. This is a treatment agent for polyester fiber tatami hem sewing thread, which is characterized by its dispersibility. The crystalline paraffin and/or natural or synthetic waxes used in the present invention include modified waxes or synthetic ester type waxes. Crystalline paraffin and various waxes at high contact pressure preferably have a melting point of 50 to 90°C. If the melting point is below 50°C, the oil film strength will be insufficient under high contact pressure and the oil film will break. Particularly when impact force is applied, the suture thread may melt and break. When the melting point is 90°C or higher, the viscosity during melting increases and frictional force tends to increase due to the generation of adhesive force. Specific examples include linear crystalline paraffin, oxidized paraffin microcrystalline wax, oxidized microcrystalline wax, carnauba wax, and synthetic ester type wax. The polyoxyalkylenealkylamine used in the present invention has the general formula [In the formula, R 1 represents a linear alkyl group having 12 to 22 carbon atoms, R 2 and R 3 represent an alkylene group having 2 to 3 carbon atoms, and 2≦m+n≦10. ] is a compound represented by R 1 in formula [1] can have carbon atoms in the range of 12 to 22, but is particularly preferably in the range of 18 to 22 carbon atoms. When the number of carbon atoms is less than 12, the smoothing properties of the lubricant are inhibited and evaporation of the lubricant solvent at high temperatures is reduced. On the other hand, when the number of carbon atoms is greater than 22, the viscosity at high temperature melting increases and the frictional force increases due to adhesive force. R 2 and R 3 in formula [1] are alkylene groups having 2 to 3 carbon atoms, and may be the same or different. When the oxyalkylene chain m+n is 11 or more, the lubricating performance is decreased and the compatibility with the lubricant is deteriorated, resulting in a significant decrease in the oil film strength improvement effect. The fatty acid used in the quaternary ammonium salt of the amide compound of fatty acid and polyalkylene polyamine used in the present invention preferably has 11 to 21 carbon atoms, and particularly preferably has 17 to 21 carbon atoms. When the number of carbon atoms is less than 11, the ability to reduce frictional force is inferior, and when the number of carbon atoms is greater than 21, the adhesive force increases when melted, resulting in a disadvantage of increasing the frictional force. Examples of polyalkylene polyamines used include diethylenetriamine, triethylenetetramine, tetraethylenepentamine, and pentaethylenehexamine. The nonionic surfactant used in the present invention is not particularly limited as long as it is nonionic; One or more types of ionic surfactants are used. The composition ratio of the treatment agent of the present invention is, for example, 70 to 90 parts by weight of various waxes, 2 to 10 parts by weight of polyoxyalkylene alkylamine, and a quaternary amide compound of fatty acid and polyalkylene polyamine to 100 parts by weight of the solid content. A range such as 2 to 10 parts by weight of ammonium salt and 10 to 25 parts by weight of nonionic surfactant can be used. When the amount of various waxes is less than 70 parts by weight, smoothness is insufficient and thread breakage may occur. If the amount exceeds 90 parts by weight, emulsification in water becomes difficult and emulsion stability deteriorates significantly, making it unusable. If the amount of polyoxyalkylene alkylamine is less than 2 parts by weight, the oil film of the lubricant will break during high contact pressure, causing thread breakage. If the amount exceeds 10 parts by weight, the smoothness decreases and normal sewing becomes impossible. If the amount of quaternary ammonium salt is less than 2 parts by weight, the dependence of smoothness on yarn speed becomes high and yarn breakage is induced when abnormal tension such as staple slip is applied.
In addition, the frictional force between fibers becomes high, making it impossible to withstand impact force. If it exceeds 10 parts by weight, the frictional force at high contact pressure will increase significantly and cause thread breakage. When nonionic surfactants are used as emulsifiers, their smoothness decreases when they absorb moisture, so it is desirable to keep the amount as small as possible, but from the standpoint of emulsion stability, it is preferable to use a nonionic surfactant that does not interfere with the sewing thread processing process. quantity needs to be used. The processing agent of the present invention is usually used in the form of an emulsion, and is optimally used at an emulsion concentration of 2 to 10% by weight. The treatment agent of the present invention is used in an amount of 1.0 to 10.0% by weight, preferably 2.0 to 10.0% by weight, based on the sewing thread in order to obtain excellent sewing performance.
When 5.0% by weight is attached, a sewing thread having excellent sewing properties suitable for sewing machines can be obtained due to the mutual effect of the wax, polyoxyalkylene alkylamine, and quaternary ammonium salt. The treatment agent of the present invention is applied to the sewing thread in the form of an emulsion, but the sewing thread usually has a total denier.
Many of them are extremely thick, measuring 3000 DE or more, and it is necessary to heat set at 160 to 200° C. under high tension after applying the treatment agent, so the immersion method is preferred as the method of applying the treatment agent. Examples will be specifically illustrated below. Note that the smoothness, stiffness, and stiffness retention after abrasion were measured by the following methods. Further, the units of composition ratios of processing agents in Examples and Comparative Examples are parts by weight unless otherwise specified, and % represents % by weight. [Smoothness] Using an Instron type tensile strength tester, fix one tatami needle to the load cell side, pass the sewing thread through the needle hole, apply a load of 5 kg, and touch it at 180° to measure 20 mm/
It is expressed as the tension when pulled at a speed of min. [Rigidity] The insertion load into a 10mm gap is expressed as rigidity using a Hou-eye meter made by Uenoyama Kiko. [Rigidity retention after abrasion] Sewing thread with 300 g of tension was applied to two S-shaped compensators and a tension controller (7
After one bar) is passed through the yarn at a yarn speed of 30 m/min, the stiffness is measured and the stiffness retention rate is calculated using the following formula. Stiffness after rubbing (g) / Stiffness before rubbing (g) x 100 = Stiffness retention rate (%) Examples 1 to 6 Three 1000 denier polyethylene terephthalate filament high tenacity yarn 250 filaments were combined and twisted. Summer. The treatment agent shown in Table 1 was applied to the sewing thread using an emulsion dipping method, and after drying with hot air at 100℃ for 10 minutes, it was heated at 200℃ under high tension.
A heat set was performed for 30 seconds. The smoothness, stiffness, and stiffness retention rate after abrasion of the thus obtained sewing thread were measured. In addition, an actual machine test was conducted using a sewing machine, and the effects shown in Table 1 were obtained. Comparative Examples 1 to 6 As shown in Table 1, Examples 1 to 6 were carried out in cases where the treatment agent does not contain any of the constituent components of the treatment agent of the present invention or the weight ratio of the treatment agent composition is outside the range of the present invention. The experiment was conducted in the same manner as in 6, and the evaluation results are shown in Table 1. The number of broken threads and number of dropped stitches in the test results using the sewing machine were counted by visual observation as follows. (1) In the case of plain stitching and backstitching The number of times the sewing machine runs out of water when flat stitching and backstitching are applied to 10 tatami mats is the number of thread breaks, and there are both sides of the plain stitching and backstitching on both sides. So (tatami) 10
(sheets) x (plain stitch) 2 (times) x (reverse stitch) 2 (times) =
This is the number of thread breakages (in total) when sewing was performed 40 times using a sewing machine. In addition, the number of dropped stitches (k) is the number of dropped stitches that are counted by visual inspection when the upper thread and lower thread do not intertwine smoothly and cause dropped stitches. (2) In the case of frame stitching In this case as well, the evaluation results are for 10 tatami mats, but since there is no turning, in this case the results are obtained when stitching is performed 10 x 2 = 20 times.
【表】【table】
【表】
実施例1〜6に示すようにワツクス、ポリオキ
シアルキレンアルキルアミン、脂肪酸とポリアル
キレンポリアミンのアマイド化合物の第4級アン
モニウム塩、非イオン系界面活性剤を配合せしめ
た本発明の処理剤を付着した縫着糸は優れた縫着
性能を示すが、比較例1〜5に示すように本発明
の処理剤からどれか1つの成分を除くなど特許請
求の範囲を外れるときは縫着性能は低下する。[Table] Treatment agent of the present invention containing wax, a polyoxyalkylene alkylamine, a quaternary ammonium salt of an amide compound of a fatty acid and a polyalkylene polyamine, and a nonionic surfactant as shown in Examples 1 to 6. The sewing thread to which is attached exhibits excellent sewing performance. However, as shown in Comparative Examples 1 to 5, when one component is removed from the treatment agent of the present invention, the sewing thread has poor sewing performance. decreases.
Claims (1)
ワツクス、ポリオキシアルキレンアルキルアミ
ン、脂肪族とポリアルキレンポリアミンとのアマ
イド化合物の第4級アンモニウム塩、非イオン系
界面活性剤を配合して乳化分散してなることを特
徴とするポリエステル繊維製畳へり縫着糸用処理
剤。 2 融点が50〜90℃の範囲にある結晶パラフイン
及び/又は天然ワツクス、変性ワツクス、合成エ
ステル型ワツクスの1種または2種以上を固型物
100重量部に対し、70〜90重量部配合せしめてな
る第1項記載の処理剤。 3 ポリオキシアルキレンアルキルアミンが一般
式 〔式中、R1は炭素数12〜22の直鎖アルキル基
を示し、R2,R3は炭素数2〜3のアルキレン基
を示し、0≦n+m≦10である。R2とR3,nと
mは同一であつても異なつていてもよい。〕で表
わされる化合物を固型物100重量部に対し2〜10
重量部配合せしめてなる第1項または第2項記載
の処理剤。 4 炭素数11〜21の脂肪酸とアミノ基3〜6個を
有するポリエチレンポリアミンとのビスアマイド
化合物をエピクロルヒドリンで縮合せしめた第4
級アンモニウム塩を固型物100重量部に対し2〜
10重量部配合せしめてなる第1項乃至第3項のい
ずれかに記載の処理剤。 5 エステル型非イオン系界面活性剤、エーテル
型非イオン系界面活性剤の1種または2種以上を
固型物100重量部に対し6〜25重量部配合せしめ
てなる第1項記載の処理剤。[Claims] 1. Crystalline paraffin and/or natural or synthetic wax, polyoxyalkylene alkylamine, quaternary ammonium salt of an amide compound of aliphatic and polyalkylene polyamine, and nonionic surfactant are blended. A treatment agent for polyester fiber tatami hem sewing thread characterized by being emulsified and dispersed. 2. One or more types of crystalline paraffin and/or natural waxes, modified waxes, and synthetic ester waxes with a melting point in the range of 50 to 90°C are solidified.
1. The processing agent according to item 1, which is blended in an amount of 70 to 90 parts by weight per 100 parts by weight. 3 Polyoxyalkylenealkylamine has the general formula [In the formula, R 1 represents a linear alkyl group having 12 to 22 carbon atoms, R 2 and R 3 represent an alkylene group having 2 to 3 carbon atoms, and 0≦n+m≦10. R 2 and R 3 and n and m may be the same or different. ] 2 to 10 parts by weight of the compound represented by
The processing agent according to item 1 or 2, wherein the treatment agent is blended in parts by weight. 4 A fourth compound prepared by condensing a bisamide compound of a fatty acid having 11 to 21 carbon atoms and a polyethylene polyamine having 3 to 6 amino groups with epichlorohydrin.
2 to 100 parts by weight of solid ammonium salt
3. The processing agent according to any one of items 1 to 3, which contains 10 parts by weight. 5. The treatment agent according to item 1, which contains 6 to 25 parts by weight of one or more of an ester type nonionic surfactant and an ether type nonionic surfactant based on 100 parts by weight of the solid material. .
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP8985682A JPS58208464A (en) | 1982-05-28 | 1982-05-28 | Treating agent for yarn stitching hem of tatami |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP8985682A JPS58208464A (en) | 1982-05-28 | 1982-05-28 | Treating agent for yarn stitching hem of tatami |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS58208464A JPS58208464A (en) | 1983-12-05 |
| JPS6249391B2 true JPS6249391B2 (en) | 1987-10-19 |
Family
ID=13982426
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP8985682A Granted JPS58208464A (en) | 1982-05-28 | 1982-05-28 | Treating agent for yarn stitching hem of tatami |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS58208464A (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH675044B5 (en) * | 1984-06-08 | 1991-02-28 | Sandoz Ag | |
| US4767646A (en) * | 1985-10-24 | 1988-08-30 | Allied Corporation | Wet abrasion resistant yarn and cordage |
| JP2664372B2 (en) * | 1987-04-08 | 1997-10-15 | 旭化成工業株式会社 | Oil agent for polyamide synthetic fiber |
-
1982
- 1982-05-28 JP JP8985682A patent/JPS58208464A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS58208464A (en) | 1983-12-05 |
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