JPH0778314B2 - Method for dyeing polyamide fiber structure - Google Patents

Method for dyeing polyamide fiber structure

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Publication number
JPH0778314B2
JPH0778314B2 JP3025664A JP2566491A JPH0778314B2 JP H0778314 B2 JPH0778314 B2 JP H0778314B2 JP 3025664 A JP3025664 A JP 3025664A JP 2566491 A JP2566491 A JP 2566491A JP H0778314 B2 JPH0778314 B2 JP H0778314B2
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JP
Japan
Prior art keywords
polyamide
dyeing
fiber structure
water
treatment
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Japanese (ja)
Other versions
JPH04214484A (en
Inventor
豊宏 田中
俊英 武田
浩 柴岡
光晴 本田
昇 各務
賢治 折山
Original Assignee
鐘紡株式会社
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Expired - Fee Related legal-status Critical Current

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Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明はポリアミド膨潤剤による
処理を行なったポリアミド系繊維の染色方法に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for dyeing polyamide fibers treated with a polyamide swelling agent.

【0002】[0002]

【従来の技術】ポリアミド系繊維はベンジルアルコール
等のポリアミド膨潤剤を付与することにより、膨潤した
り、これと加熱処理とを組合せることにより、収縮を生
じたりするため、これら作用を用いて、フィブリル化
(極細化)布帛や、高密度化布帛等を製造することが種
々提案されている(例えば特公昭53−35633号公
報や特公昭61−37383号公報)。
2. Description of the Related Art Polyamide fibers are swollen by applying a polyamide swelling agent such as benzyl alcohol, or contracted by combining this with heat treatment. Various proposals have been made for producing fibrillated (ultrafine) fabrics, densified fabrics and the like (for example, Japanese Patent Publication No. 53-35633 and Japanese Patent Publication No. 61-37383).

【0003】かかるポリアミド膨潤剤使用布帛は、ポリ
アミド膨潤剤が布帛中に残存したまま染色を行なうと堅
牢度の低下が著しい点が問題であって、従来は、水洗
(ソーピング)を充分に行ないポリアミド膨潤剤を除去
する方法や、染色後オキシスルホン酸塩縮合物等を用い
てフィックス処理を行なう方法等が知られていた。
A problem with such a fabric containing a polyamide swelling agent is that if dyeing is carried out with the polyamide swelling agent remaining in the fabric, the fastness is markedly deteriorated. Conventionally, a polyamide which has been sufficiently washed with water (soaping) is used. A method of removing the swelling agent, a method of performing a fixing treatment using an oxysulfonate condensate after dyeing, and the like have been known.

【0004】[0004]

【発明が解決しようとする課題】しかしながら、ソーピ
ングやフィックス処理では充分な染色堅牢度を維持する
ことは困難である。特に、本発明者らが特願平1−31
6924号として提案した、ポリアミド系繊維を用いた
繊維構造物をポリアミド膨潤剤の溶液流中で循環移動せ
しめて高密度化させた布帛の場合、染色堅牢度の低下が
著しくソーピングやフィックス処理のみでは実用に耐え
得る染色品を得ることが困難であった。
However, it is difficult to maintain a sufficient dyeing fastness by soaping or fixing treatment. In particular, the present inventors
In the case of a fabric proposed as No. 6924, which is densified by circulating and moving a fiber structure using a polyamide-based fiber in a solution flow of a polyamide swelling agent, the dyeing fastness is remarkably lowered and only by soaping or fixing treatment. It has been difficult to obtain a dyed product that can be used practically.

【0005】本発明はかかる問題点を解決するものであ
って、前記の如きポリアミド系布帛の染色堅牢度を向上
せしめ、実用に耐え得るこれら染色品を提供することを
目的とする。
The present invention has been made to solve the above problems, and an object of the present invention is to improve the dyeing fastness of the polyamide cloth as described above and to provide these dyed articles which can be used practically.

【0006】[0006]

【課題を解決するための手段】本発明は、ポリアミド系
繊維を用いた繊維構造物にポリアミド膨潤剤を付与して
処理し、水洗,乾燥後、更に水の共存下で100〜19
0℃の加熱処理を行ない、次いで染色することを特徴と
するものである。
According to the present invention, a fiber swelling agent using a polyamide fiber is treated with a polyamide swelling agent, washed with water and dried, and then in a coexistence with water of 100 to 19.
It is characterized in that it is subjected to heat treatment at 0 ° C. and then dyed.

【0007】本発明で用いるポリアミドとしては、例え
ば、ナイロン4,ナイロン6,ナイロン7,ナイロン1
1,ナイロン12,ナイロン66,ナイロン610,ポ
リメタキシレンアジパミド,ポリパラキシリレンデカン
アミド,ポリビスシクロヘキシルメタンデカンアミド及
びそれらを成分とするコポリアミドが挙げられるが、ナ
イロン6,ナイロン66が好ましい。
As the polyamide used in the present invention, for example, nylon 4, nylon 6, nylon 7, nylon 1
1, Nylon 12, Nylon 66, Nylon 610, Polymethaxylene adipamide, Polyparaxylylene decanamide, Polybiscyclohexylmethane decanamide and copolyamides containing them are examples of nylon 6, nylon 66. preferable.

【0008】これらポリアミドは、単独で紡糸して単糸
繊度0.5〜8デニール程度の糸条となしても、ポリエ
チレンテレフタレートやアルカリ易溶解の共重合ポリエ
ステル等と複合紡糸してもよい。又、本発明に云う繊維
構造物とは、織物,編物,不織布等であり、その主要構
成素材が前記ポリアミドであれば、ポリエステル,綿,
絹,羊毛等の他繊維を混用してもよい。ただ、前記の如
くポリアミド成分の比率が大きい程染色堅牢度低下の問
題が大きいことからみて、繊維構造物に対してポリアミ
ド成分が70重量%以上のものの場合効果が大きい。
These polyamides may be spun singly to form a single yarn fineness of about 0.5 to 8 denier, or may be composite spun with polyethylene terephthalate or a copolymer polyester easily soluble in alkali. The fiber structure referred to in the present invention is a woven fabric, a knitted fabric, a non-woven fabric or the like, and if the main constituent material thereof is the above-mentioned polyamide, polyester, cotton,
Other fibers such as silk and wool may be mixed. However, as described above, the higher the ratio of the polyamide component is, the greater the problem of deterioration in dyeing fastness is. Therefore, when the polyamide component is 70% by weight or more with respect to the fiber structure, the effect is large.

【0009】次に本発明で用いるポリアミド膨潤剤とし
ては、ベンジルアルコール,フェノール,ギ酸,酢酸,
ジメチルホルムアミド,キシレン等のエマルジョンが挙
げられ、特にベンジルアルコールのエマルジョンが好ま
しい。かかるポリアミド膨潤剤のエマルジョン化に際し
ては、ノニオン系,カチオン系,アニオン系又はこれら
の混合型の界面活性剤を添加して乳化分散させればよ
い。ポリアミド膨潤剤は、ポリアミド繊維構造物をポリ
アミド膨潤剤溶液流中で処理して高密度化する場合は、
1〜10重量%程度の低濃度溶液として、これを若干高
めの温度即ち、60〜100℃程度で用いるとよく、そ
の際アニオン成分を増強する等して高温域の乳化力を向
上せしめた乳化剤を用いることが好ましい。
Next, the polyamide swelling agent used in the present invention includes benzyl alcohol, phenol, formic acid, acetic acid,
Examples thereof include emulsions of dimethylformamide, xylene and the like, and an emulsion of benzyl alcohol is particularly preferable. When emulsifying such a polyamide swelling agent, a nonionic, cationic, anionic or mixed surfactant thereof may be added and emulsified and dispersed. When the polyamide swelling agent is treated to densify the polyamide fiber structure in the polyamide swelling agent solution flow,
As a low-concentration solution of about 1 to 10% by weight, this solution may be used at a slightly higher temperature, that is, about 60 to 100 ° C., and at that time, an anionic component is enhanced to improve the emulsifying power in a high temperature range. Is preferably used.

【0010】ポリアミド膨潤剤を付与して処理した後
は、従来と同様水洗,乾燥工程によりポリアミド膨潤剤
を一応除去する。本発明で重要なことは、これら処理に
引続き、水の共存下で100℃以上の加熱処理を行うこ
とである。かかる処理を具体的に説明すると、乾燥を経
た繊維構造物に水分を付与する。水分はアルコール,フ
ェノール,有機酸,ジメチルホルムアミド,キシレン等
を実質的に含有しないものが好ましく、付与量は繊維構
造物に対して、20〜100重量%程度が適当である。
After the polyamide swelling agent is applied and treated, the polyamide swelling agent is temporarily removed by washing and drying steps as in the conventional case. What is important in the present invention is that following these treatments, heat treatment at 100 ° C. or higher is performed in the coexistence of water. Explaining this treatment in detail, moisture is applied to the dried fiber structure. The water content is preferably substantially free of alcohol, phenol, organic acid, dimethylformamide, xylene and the like, and the amount of water added is appropriately about 20 to 100% by weight based on the fiber structure.

【0011】又、付与方法は、水分が充分繊維構造物中
に浸透するようマングルによるパッディング法等を用い
るのがよい。水分を付与した後は、水分を保持したまま
直ちにこれを100℃以上に加熱する。190℃を超え
るとポリアミド成分のゼイ化が激しいので、100〜1
90℃の範囲に留める。
Further, as the applying method, it is preferable to use a padding method using a mangle so that the water sufficiently penetrates into the fiber structure. After the water is applied, it is immediately heated to 100 ° C. or higher while keeping the water. When the temperature exceeds 190 ° C, the polyamide component is severely zeated, so 100 to 1
Keep in the 90 ° C range.

【0012】又、加熱方法も、熱ヒータ,テンター,シ
ュリンクサーファー等を用いた乾熱法の他、高温高圧ス
チーマを用いて加熱水蒸気中で処理する湿熱法等が挙げ
られるが、乾熱法が好ましい。加熱処理は、乾熱法で
0.5〜5分間、湿熱法で1〜10分間程度行なうとよ
い。
The heating method includes a dry heat method using a heat heater, a tenter, a shrink surfer, etc., and a wet heat method of treating in heated steam using a high temperature and high pressure steamer. preferable. The heat treatment may be performed by a dry heat method for 0.5 to 5 minutes and a wet heat method for about 1 to 10 minutes.

【0013】加熱処理後は、常法に従い酸性染料,反応
性染料,金属醋塩染料等で繊維構造物を染色する。
After the heat treatment, the fiber structure is dyed with an acid dye, a reactive dye, a metal acetate dye or the like according to a conventional method.

【0014】以上の処理により、堅牢度に優れた染色品
が得られるが、更に染色堅牢度を向上させるためには、
以下の処理を引続いて行うとよい。即ち、染着せるポリ
アミド繊維に対し第一浴としてタンニン酸水溶液、第二
浴としてアルミン酸ソーダ水溶液を使用して染料の固着
を行う処理である。かかる処理に関しては、特公昭43
−20968号公報にも記載があるが、同公報に記載さ
れた条件よりもタンニン酸の濃度を高くすることが好ま
しく、繊維重量に対して0.5〜12重量%、より好ま
しくは1.0〜7.0重量%付与するとよい。又、使用
するタンニン酸は、通常のタンニン酸並びに合成タンニ
ン剤であって、同様に適用することができる。
By the above treatment, a dyed product having excellent fastness can be obtained. To further improve the fastness of dyeing,
The following processing may be continuously performed. That is, this is a treatment in which the dye is fixed to the polyamide fiber to be dyed using the tannic acid aqueous solution as the first bath and the sodium aluminate aqueous solution as the second bath. Regarding such processing, Japanese Patent Publication No. 43
As described in JP-A-20968, it is preferable to increase the concentration of tannic acid as compared with the conditions described in JP-A-20968, and it is preferably 0.5 to 12% by weight, more preferably 1.0. It is recommended to add about 7.0% by weight. The tannic acid to be used is a usual tannic acid or a synthetic tannin agent and can be applied in the same manner.

【0015】またタンニン酸で処理する場合、処理浴中
に添加する酸類として酢酸,ギ酸などの有機酸や塩酸な
どの従来公知の酸類が適用される。
When treating with tannic acid, conventionally known acids such as organic acids such as acetic acid and formic acid and hydrochloric acid are applied as the acids to be added to the treatment bath.

【0016】アルミン酸ソーダ処理に於けるアミン酸ソ
ーダ濃度は対繊維重量で0.1〜6.0%が適し、最適
濃度は0.5〜4.0%の範囲である。
The concentration of sodium amine acid in the treatment with sodium aluminate is preferably 0.1 to 6.0% based on the weight of fiber, and the optimum concentration is in the range of 0.5 to 4.0%.

【0017】またその場合浴比は1:20〜1:100
の範囲が適し、処理温度は20〜90℃が適当である。
アルミン酸ソーダ濃度は前記の範囲外では固着効果は少
く、また過剰では処理中及び処理後に於ける染料の脱落
量は増大するので好ましくない。
In that case, the bath ratio is 1:20 to 1: 100.
Is suitable, and the treatment temperature is suitably 20 to 90 ° C.
When the concentration of sodium aluminate is outside the above range, the fixing effect is small, and when the concentration is excessive, the amount of dye lost during and after the treatment increases, which is not preferable.

【0018】[0018]

【実施例】堅牢度は以下の方法により測定した。 (1) 耐光堅牢度 JIS−L−0842 4級試験 (1) 洗濯堅牢度 JIS−L−0844 A−2号 (3) ドライクリーニング堅牢度 JIS−L−0860 尚%は特に明記しない限り重量%を示す。[Example] Fastness was measured by the following method. (1) Lightfastness JIS-L-0842 Class 4 test (1) Washing fastness JIS-L-0844 A-2 (3) Dry cleaning fastness JIS-L-0860 Unless otherwise specified,% is% by weight. Indicates.

【0019】実施例1 115D/72Fの6ナイロンマルチフィラメント糸を
経緯糸に用いて経119本/インチ,緯86本/インチ
の平織生機を得た。
Example 1 A plain weaving loom having a warp of 119 yarns / inch and a weft of 86 yarns / inch was obtained by using 115D / 72F 6 nylon multifilament yarn as the warp yarn.

【0020】得られた生機を液流染色機(日阪製作所タ
テ型サーキュラ)に仕掛け、ベンジルアルコール5.0
%,乳化剤(竹本油脂製KM−240)0.5%からな
るエマルジョン溶液で処理した。即ち、染色機を作動さ
せて生機を循環移動せしめつつ、エマルジョン溶液を3
0分間で80℃まで昇温し、このまま更に30分間処理
を続けた後、エマルジョン溶液を排出回収して水洗,乾
燥し、経方向に21%、緯方向に17%収縮せしめた高
密度織物を得た。
The resulting greige was set on a jet dyeing machine (Vertical Circular, manufactured by Hisaka Seisakusho), and benzyl alcohol 5.0
%, And an emulsifier solution (KM-240 manufactured by Takemoto Yushi Co., Ltd.) 0.5%. That is, while operating the dyeing machine to circulate the raw fabric, the emulsion solution is
After raising the temperature to 80 ° C. in 0 minutes and continuing the treatment for 30 minutes as it is, the emulsion solution is discharged and collected, washed with water and dried to obtain a high-density fabric shrinking 21% in the warp direction and 17% in the weft direction. Obtained.

【0021】次いで、かかる織物をパッダーに掛け、ピ
ックアップ率50%で水を付与した後、直ちにテンター
に供給して180℃で2分間乾熱処理を行ない、次いで
酸性染料を用いてベージュに染色した。結果を表1に示
す。
Then, the woven fabric was put on a padder, water was applied at a pick-up rate of 50%, immediately supplied to a tenter and subjected to dry heat treatment at 180 ° C. for 2 minutes, and then dyed in beige with an acid dye. The results are shown in Table 1.

【0022】実施例2 実施例1で得られた高密度織物を、パッダーに掛けてピ
ックアップ率60%で水を付与し、直ちに高温高圧スチ
ーマ(山東鉄工製)に供給して120℃で2分間湿熱処
理(加熱水蒸気)を行ない、実施例1と同様ベージュに
染色した。結果を表1に示す。
Example 2 The high-density fabric obtained in Example 1 was hung on a padder, water was applied at a pick-up rate of 60%, and immediately supplied to a high-temperature high-pressure steamer (manufactured by Shanto Tekko Co., Ltd.) at 120 ° C. for 2 minutes. Wet heat treatment (heated steam) was performed, and dyeing was performed in the same manner as in Example 1 to beige. The results are shown in Table 1.

【0023】比較例1,2 実施例1においてパッダーによる水付与処理,乾熱処理
を行なわず染色を行なったもの(比較例1)、パッダー
による水付与処理を行なわず、乾熱処理,染色を行なっ
たもの(比較例2)について結果を表1に示す。
Comparative Examples 1 and 2 What was dyed without water-adding treatment with a padder and dry heat treatment in Example 1 (Comparative Example 1), and dry-heat treatment and dyeing without water-feeding treatment with a padder The results are shown in Table 1 for the product (Comparative Example 2).

【表1】 [Table 1]

【0024】実施例3〜8 実施例1において染料を表2の如く用いて染色した後、
タンニン酸6%,酢酸3%の水溶液で浴比1:50で、
60℃×20分間処理した後、更にアルミン酸ソーダ浴
(アルミン酸ソーダ3.5%owf,浴比1:50)で
20分間処理を行なったもの(実施例3〜5)及び、タ
ンニン酸6%水溶液60℃で20分間処理した後、吐酒
石3%水溶液60℃で20分間処理を行なったもの(実
施例6〜8)について結果を表2に示す。
Examples 3 to 8 After dyeing using the dyes shown in Table 2 in Example 1,
An aqueous solution of 6% tannic acid and 3% acetic acid in a bath ratio of 1:50,
After being treated at 60 ° C. for 20 minutes, it was further treated in a sodium aluminate bath (sodium aluminate 3.5% owf, bath ratio 1:50) for 20 minutes (Examples 3 to 5) and tannic acid 6 % Aqueous solution at 60 ° C. for 20 minutes and then 3% tartarite aqueous solution at 60 ° C. for 20 minutes (Examples 6 to 8).

【0025】[0025]

【表2】 [Table 2]

【0026】実施例9,10,比較例3 経糸に60番手単糸の羊毛と30デニールの6ナイロン
フィラメント糸の交撚糸を、緯糸に80番手双糸の羊毛
を用いて、経96本/インチ,緯61本/インチ,目付
167g/m2 の平織生機を得た(実施例9)。
Examples 9 and 10, Comparative Example 3 96 warps / inch using warp yarns of 60-count single yarn wool and 30-denier 6 nylon filament yarn intertwisted yarn and weft yarns of 80-count twin yarn. A plain weave machine having a weft of 61 yarns / inch and a basis weight of 167 g / m 2 was obtained (Example 9).

【0027】一方、経糸に80番手双糸の羊毛、緯糸に
100デニールの6ナイロンフィラメント糸を用いて、
経107本/インチ,緯72本/インチ,目付200g
/m2 の綾織生機を得た(実施例10)。
On the other hand, using 80-count double-ply wool as the warp and 100 denier 6 nylon filament yarn as the weft,
Warp 107 lines / inch, weft 72 lines / inch, basis weight 200g
A twill weaving machine of / m 2 was obtained (Example 10).

【0028】得られた生機を液流染色機(日阪製作所タ
テ型サーシュラ)に仕掛け、ベンジルアルコール10.
0%,乳化剤(竹本油脂製 KM−240)1.0%か
らなるエマルジョン溶液で処理した。即ち、染色機を作
動させて生機を循環移動せしめつつ、エマルジョン溶液
を30分間で80℃まで昇温し、このまま更に30分間
処理を続けた後、エマルジョン溶液を排出回収して水
洗,乾燥し、実施例9では経方向に27%,緯方向に2
%、又、実施例10では経方向1%,緯方向21%収縮
せしめた高密度織物を得た。
The resulting greige fabric was set on a jet dyeing machine (Versa Saura by Hizaka Seisakusho), and benzyl alcohol was added.
It was treated with an emulsion solution consisting of 0% and 1.0% of an emulsifier (KM-240 manufactured by Takemoto Yushi Co., Ltd.). That is, while operating the dyeing machine and circulatingly moving the raw fabric, the emulsion solution was heated to 80 ° C. for 30 minutes, and after the treatment was continued for another 30 minutes, the emulsion solution was discharged and recovered, washed with water, and dried. In Example 9, 27% in the warp direction and 2 in the weft direction.
%, And in Example 10, a high-density woven fabric was obtained which was shrunk by 1% in the warp direction and 21% in the weft direction.

【0029】次いで、かかる織物をパッダーに掛け、ピ
ックアップ率50%で水を付与した後、直ちにテンター
に供給して180℃で2分間乾熱処理を行ない、次いで
酸性染料(Everacid milling Red RS 2%owf)で染
色した。かかる織物の染色堅牢度を表3に示す。
Next, such a woven fabric is put on a padder, water is applied at a pick-up rate of 50%, and then immediately fed to a tenter to perform a dry heat treatment at 180 ° C. for 2 minutes, and then an acid dye (Everacid milling Red RS 2% owf ). The dyeing fastness of such a fabric is shown in Table 3.

【0030】[0030]

【表3】 [Table 3]

【0031】又、実施例9の織物についてベンジルアル
コールによる処理を行なわない織物を得た(比較例
3)。 これら織物について羊毛及びナイロンの染着濃度を測定
し、次の式でK/Sを算出した。 K/S:見掛け濃度 R:最大吸収波長の反射率 結果を表4に示す。
A woven fabric obtained by not treating the woven fabric of Example 9 with benzyl alcohol was obtained (Comparative Example 3). The wool and nylon dyeing densities of these fabrics were measured, and K / S was calculated by the following formula. K / S: apparent density R: reflectance at maximum absorption wavelength The results are shown in Table 4.

【0032】[0032]

【表4】 [Table 4]

【0033】表4に示す如く、ベンジルアルコール処理
を行なったものは染着濃度差が少なく同色性が高い。
As shown in Table 4, those treated with benzyl alcohol have a small difference in dyeing density and high color uniformity.

【0034】又、実施例9においてベンジルアルコール
濃度を変化せしめた際の、羊毛及びナイロンのK/Sの
変化を図1に示す。更に同例において、染料をNeutrich
romeRed S-GN 2%owfに変え同様に処理を行った際
のK/Sの変化を図2に示す。
FIG. 1 shows the changes in K / S of wool and nylon when the concentration of benzyl alcohol was changed in Example 9. Further in the same example, the dye was Neutrich
Fig. 2 shows the change in K / S when the same treatment was performed by changing to romeRed S-GN 2% owf.

【0035】[0035]

【発明の効果】本発明によれば、ポリアミド繊維をポリ
アミド膨潤剤で処理した付加価値の高い繊維構造物の染
色堅牢度を、容易に実用レベルまで高めることができ、
その有用性は明らかである。
According to the present invention, the dyeing fastness of a high-value-added fiber structure obtained by treating a polyamide fiber with a polyamide swelling agent can be easily increased to a practical level.
Its usefulness is clear.

【0036】更に、羊毛と混用した繊維構造物に適用す
れば、ポリアミドとの間で均一な染色が行ない得、堅牢
度の向上と相俟って極めて品位の高い染色物を得ること
ができる。
Further, when it is applied to a fiber structure mixed with wool, uniform dyeing can be carried out with polyamide, and an extremely high quality dyeing can be obtained in combination with the improvement of fastness.

【図面の簡単な説明】[Brief description of drawings]

【図1】ベンジルアルコール濃度を変化せしめた際の羊
毛及びナイロンのK/S変化を示すグラフ。
FIG. 1 is a graph showing the K / S change of wool and nylon when the benzyl alcohol concentration is changed.

【図2】図1において染料を変えた際の同グラフ。FIG. 2 is the same graph when the dye is changed in FIG.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 D06P 5/00 103 // D06M 11/05 13/144 D06M 101:34 (56)参考文献 特開 昭48−28785(JP,A) 特開 昭58−36285(JP,A) 特公 昭38−23293(JP,B1) 特公 昭50−30755(JP,B1)─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 6 Identification number Internal reference number FI Technical display location D06P 5/00 103 // D06M 11/05 13/144 D06M 101: 34 (56) References 48-28785 (JP, A) JP 58-36285 (JP, A) JP 38-23293 (JP, B1) JP 50-30755 (JP, B1)

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 ポリアミド系繊維を用いた繊維構造物に
ポリアミド膨潤剤を付与して処理し、水洗,乾燥後、更
に水の共存下で100〜190℃の加熱処理を行ない、
次いで染色することを特徴とするポリアミド繊維構造物
の染色方法。
1. A fiber structure using a polyamide fiber is treated with a polyamide swelling agent, washed with water, dried, and then subjected to heat treatment at 100 to 190 ° C. in the coexistence of water.
A method for dyeing a polyamide fiber structure, which comprises dyeing subsequently.
JP3025664A 1990-07-25 1991-01-24 Method for dyeing polyamide fiber structure Expired - Fee Related JPH0778314B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3025664A JPH0778314B2 (en) 1990-07-25 1991-01-24 Method for dyeing polyamide fiber structure

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP2-196567 1990-07-25
JP19656790 1990-07-25
JP3025664A JPH0778314B2 (en) 1990-07-25 1991-01-24 Method for dyeing polyamide fiber structure

Publications (2)

Publication Number Publication Date
JPH04214484A JPH04214484A (en) 1992-08-05
JPH0778314B2 true JPH0778314B2 (en) 1995-08-23

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Country Status (1)

Country Link
JP (1) JPH0778314B2 (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5671277B2 (en) * 2010-08-09 2015-02-18 岐セン株式会社 Aramid fiber dyeing method
JP5844537B2 (en) * 2011-03-30 2016-01-20 帝人株式会社 Aramid fiber dyeing method
JP5730110B2 (en) * 2011-04-13 2015-06-03 小松精練株式会社 Fabric manufacturing method and fiber fabric

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4828785A (en) * 1971-08-19 1973-04-16
JPS5030755A (en) * 1973-07-23 1975-03-27
JPS5836285A (en) * 1981-08-26 1983-03-03 小松精練株式会社 Dyeing of polyamide fiber fabric

Also Published As

Publication number Publication date
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