JP4443856B2 - Polyester fabric for pitting process - Google Patents

Polyester fabric for pitting process Download PDF

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Publication number
JP4443856B2
JP4443856B2 JP2003143120A JP2003143120A JP4443856B2 JP 4443856 B2 JP4443856 B2 JP 4443856B2 JP 2003143120 A JP2003143120 A JP 2003143120A JP 2003143120 A JP2003143120 A JP 2003143120A JP 4443856 B2 JP4443856 B2 JP 4443856B2
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JP
Japan
Prior art keywords
ethylene oxide
paste
fabric
polyester
polyhydric alcohol
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 - Lifetime
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JP2003143120A
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Japanese (ja)
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JP2004346444A (en
Inventor
洋和 西澤
秀康 寺尾
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
Mitsubishi Rayon Co Ltd
Mitsubishi Rayon Textile Co Ltd
Original Assignee
Mitsubishi Chemical Corp
Mitsubishi Rayon Co Ltd
Mitsubishi Rayon Textile Co Ltd
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Priority to JP2003143120A priority Critical patent/JP4443856B2/en
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Publication of JP4443856B2 publication Critical patent/JP4443856B2/en
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  • Chemical Or Physical Treatment Of Fibers (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Description

【0001】
【発明の属する技術分野】
本発明は、抜蝕加工用のポリエステル布帛に関する。
【0002】
【従来の技術】
従来より、溶解性の異なるポリエステル繊維からなる繊維構造物に減量促進剤を含有する糊剤を印捺した後、片方のポリエステル繊維を部分的に溶解して透かし模様を得る,いわゆる抜蝕加工が行われている。
【0003】
抜蝕加工における減量促進剤についても種々検討されているが、変性ポリエステルポリマーからなる繊維と未変性ポリエステルポリマーからなる繊維を含んだ繊維構造物や、変性ポリエステルポリマーと未変性ポリエステルポリマーの複合紡糸繊維からなる繊維構造物等の場合、公知の減量促進剤である第四級アンモニウム塩を用いると、染斑の発生、発泡による作業性低下、アルカリ減量で未変性ポリエステル繊維或いは複合繊維の未変性ポリエステル成分まで減量が促進され、繊維構造物としての強力低下を生ずる等の問題点がある。
【0004】
このため、特許文献1では、多価アルコールにエチレンオキシドを2モル以上付加して生成された多価アルコールエチレンオキシド付加物を含む糊剤を印捺した布帛が記載されている。
【0005】
【特許文献1】
特開平7−189117号公報
【0006】
【発明が解決しようとする課題】
しかしこの方法では、アルカリ減量時間が短い、あるいはアルカリ濃度が低い場合には、アルカリ減量による抜蝕が不十分になりやすかった。また、抜蝕を充分に行いシャープな透かし模様を得るため、アルカリ濃度を高く、あるいは減量時間を長くした場合は、糊剤を印捺していない部分もアルカリ減量により溶解し、糊剤を印捺した目的の部分が溶解したシャープな透かし模様が得られにくかった。
【0007】
本発明は、上記問題点を解決することを目的とするもので、糊剤を印捺してない部分のポリエステル繊維部分のアルカリ減量速度に対して、糊剤を印捺した部分のポリエステル繊維のアルカリ減量速度を著しく速くすることで、シャープな透かし模様が得られる抜蝕加工用ポリエステル布帛を提供するものである。
【0008】
【課題を解決するための手段】
本発明の要旨は、多価アルコールにエチレンオキシドを2モル以上付加した多価アルコールエチレンオキシド付加物と第四級アンモニウム塩を含有する糊剤であって、多価アルコールエチレンオキシド付加物を糊剤100g当たり1〜50g、第四級アンモニウム塩を糊剤100g当たり0.5〜10g含有する糊剤が付着した抜蝕加工用ポリエステル布帛にある。
【0009】
【発明の実施の形態】
本発明の抜蝕加工用ポリエステル布帛は、多価アルコールにエチレンオキシドを2モル以上付加した多価アルコールエチレンオキシド付加物と第四級アンモニウム塩を含有する糊剤が付着していることが必要である。
【0010】
本発明では、多価アルコールエチレンオキシド付加物と第四級アンモニウム塩を併用する糊剤を用いることにより、該糊剤が付着した部分の減量を促進し、シャープな透かし模様を得ることが可能となる。
【0011】
本発明の多価アルコールエチレンオキシド付加物としては、エチレングリコール、プロピレングリコール、ヒドロベンゾイン、ベンゾピナコール、シクロペンタンー1,2−ジオール、シクロヘキサンー1,4−ジオール等の二価アルコール、グリセリン等の三価アルコールに、エチレンオキシドを2モル以上付加した生成物が用いられる。
【0012】
本発明において好ましく用いられる多価アルコールエチレンオキシド付加物としては、エチレングリコールのエチレンオキシド5〜30モル付加物、グリセリンのエチレンオキシド3〜28モル付加物が挙げられる。
【0013】
第4級アンモニウム塩としては、ポリエステル繊維に対してアルカリ減量促進効果のあるものなら特に限定はないが、特に[RN(CH)(CHCHO)mH)(CHCHO)nH)]Cl(Rは炭素数12〜18のアルキル基、m+nは2〜30の間に含まれる数)の構造式を有する第四級アンモニウム塩の一種または二種以上が好ましい。また、式中m+nの値が30を超えると減量促進効果が弱くなりやすい。
【0014】
また本発明では、多価アルコールエチレンオキシド付加物が、糊剤100g当たり1〜50g好ましくは5〜20g、第四級アンモニウム塩が糊剤100g当たり0.5〜10g好ましくは1〜3g含有された糊剤が付着していることが好ましい。
【0015】
多価アルコールエチレンオキシド付加物が、糊剤100g当たり1g未満では印捺部の減量促進効果が不十分であり、抜蝕部と非抜蝕部の減量差が小さくシャープな模様がえられ難く、糊剤100g当たり50gを超えると多価アルコールエチレンオキシド付加物が非印捺部に滲み出し印捺の型際が不鮮明になる。
【0016】
第四級アンモニウム塩の量が糊剤100g当たり0.5g未満では、多価アルコールエチレンオキシド付加物との併用による効果が不十分で、目的とするシャープな模様が得られにくい。
【0017】
また、糊剤100g当たり10gを超えると、発泡を生じ作業性が悪くなりやすく、抜蝕加工後の布帛の強度も低下しやすい。
【0018】
なお本発明の糊剤の主成分としては、小麦粉、トラガントガム、ローカストビーンガム、カルボキシメチルセルロース、ポリビニルアルコール、ポリアクリル酸ソーダ等が挙げられ、これらを単独または2種以上混合して用いてもよい。
【0019】
さらに本発明の抜蝕加工用ポリエステル布帛は、ポリエステル繊維を含む布帛であればよいが、第三成分を1〜15モル%共重合した変性ポリエステル繊維と、第三成分が0.5モル%以下の未変性ポリエステル繊維を含むことが、抜蝕加工によりシャープな透かし模様を得るために好ましい。
【0020】
変性ポリエステル繊維としては、アルカリ金属スルホン酸基を有する第三成分により変性されたポリエステル繊維が好ましく、5−ナトリウムスルホイソフタル酸と、アジピン酸、セバシン酸等の脂肪族ジカルボン酸を共重合させたポリエチレンテレフタレート、特に好ましくは5−ナトリウムスルホソフタル酸1.5〜4モル%とアジピン酸3〜13モルを共重合させたポリエチレンテレフタレートからなポリエステル繊維が挙げられる。
【0021】
なお本発明の抜蝕加工用ポリエステル布帛は、ポリエステル系繊維を含む布帛に、任意の方法で糊剤を付着することにより得られるが、印捺による方法が好ましい。印捺は公知の任意の方法で、模様等の部分印捺、あるいは全面の印捺等、任意に行うことができる。
【0022】
印捺方法は、フラットスクリーン捺染、ロータリスクリーン−捺染、ローラー捺染、ビゴロ捺染、インクジェット捺染等が挙げられる。
【0023】
本発明の抜蝕加工用ポリエステル布帛は、熱処理後にアルカリ水溶液で処理することにより、糊剤が付着した部分を優先的にアルカリ減量し、シャープな透かし模様を得ることが可能となる。
【0024】
熱処理の温度は100〜200℃が必要である。熱処理温度が100℃未満では減量促進剤が変性ポリエステル中に含侵されず減量促進効果が不充分となりシャープな模様が得られず、200℃を超えるとポリエステルの風合が硬化する。
【0025】
熱処理は乾熱または湿熱で行い、乾熱の場合は30秒〜5分、湿熱の場合は30秒〜30分が好ましい。
【0026】
アルカリ水溶液としては水酸化ナトリウム、水酸化カリウム等のアルカリ金属水酸化物、水酸化マグネシウム、水酸化カルシウム等のアルカリ土類金属水酸化物等の水溶液を用い、必要によりトリエタノールアミン、ジエタノールアミン、モノエタノールアミン等のアミンを併用しても良い。
【0027】
アルカリ水溶液による減量条件は、ポリエステル繊維のポリマー組成、品種等によっても異なるが、水酸化ナトリウム水溶液の場合、濃度は0.3〜3質量%、好ましくは1.5質量%以下。温度は80〜130℃、好ましくは90〜105℃、浴比1:5以上好ましくは1:30以上で実施する。
【0028】
【実施例】
以下に本発明を実施例により具体的に説明する。
【0029】
(実施例1)
変性ポリエステル繊維として、5−Naスルホイソフタル酸2.25モル%およびアジピン酸5モル%を共重合したポリマーからなる84dtex/48fの三角断面糸を仮撚温度160℃で通常の仮撚加工を施したものを、未変性ポリエステル繊維として、ポリエチレンテレフタレートのみからなる22dtex/1fの丸断面糸を準備した。
【0030】
経糸に該未変性ポリエステル繊維を単独で用い、緯糸に該変性ポリエステル繊維と該未変性ポリエステル繊維とを撚数120T/Mで合撚したものを用い、経糸密度120本/吋、緯糸密度115本/吋の平織物を作成した。
【0031】
得られた平織物に下記の、多価アルコールにエチレンオキシドを2モル以上付加した多価アルコールエチレンオキシド付加物と第四級アンモニウム塩を含有する下記の糊剤を柄状に印捺し抜蝕加工用ポリエステル布帛を得た。
【0032】
得られた抜蝕加工用ポリエステル布帛を、110℃で2分間乾燥後、温度190℃の乾熱雰囲気下にて2分間熱処理した後、水酸化ナトリウム1%水溶液で浴比1:50、100℃で45分間アルカリ処理し、常法により洗浄、中和、乾燥した。
【0033】
得られた平織物の糊剤の印捺部は、変性ポリエステル繊維がアルカリ処理により完全に溶解除去されており、型際の極めてシャープな透かし模様を有する抜蝕加工布帛が得られた。
【0034】
糊剤
グリセリンエチレンオキシド10モル付加物・・・10重量部
[C1225N(CH)(CHCHO)mH)(CHCHO)nH)]Cl(m+n=2〜8の混合品)・・・2.5重量部
ファインガムG17(第一工業製薬(株)社製 糊剤)・・・6重量部
水・・・81.5重量部
(比較例1)
下記の第四級アンモニウム塩を含有しない糊剤を用いた以外は、実施例1と同様にして、抜蝕加工用ポリエステル布帛を得て抜蝕加工を行った。
【0035】
得られた平織物は、糊剤の印捺部の変性ポリエステル繊維が完全に除去されておらず、シャープな透かし模様が得られなかった。
【0036】
糊剤
グリセリンエチレンオキシド10モル付加物・・・10重量部
ファインガムG17(第一工業製薬(株)社製 糊剤)・・・6重量部
水・・・84重量部
【0037】
【発明の効果】
本発明の抜蝕加工用ポリエステル布帛はアルカリ減量による抜蝕加工により、シャープな透かし模様が得られる。
[0001]
BACKGROUND OF THE INVENTION
The present invention relates to a polyester fabric for pitting processing.
[0002]
[Prior art]
Conventionally, so-called discharge processing is performed, in which after a paste containing a weight loss accelerator is printed on a fiber structure composed of polyester fibers having different solubility properties, one polyester fiber is partially dissolved to obtain a watermark pattern. Has been done.
[0003]
Although various investigations have been made on weight loss accelerators in pitting processing, fiber structures including fibers made of modified polyester polymers and fibers made of unmodified polyester polymers, and composite spun fibers of modified polyester polymers and unmodified polyester polymers When using a quaternary ammonium salt, which is a known weight loss accelerator, in the case of a fiber structure composed of, unmodified polyester fiber or unmodified polyester of composite fiber due to occurrence of dyeing spots, reduced workability due to foaming, alkali weight loss There is a problem that weight loss is promoted to the components and the strength of the fiber structure is reduced.
[0004]
For this reason, Patent Document 1 describes a fabric printed with a paste containing a polyhydric alcohol ethylene oxide adduct produced by adding 2 mol or more of ethylene oxide to polyhydric alcohol.
[0005]
[Patent Document 1]
JP-A-7-189117 [0006]
[Problems to be solved by the invention]
However, in this method, when the alkali weight loss time is short or the alkali concentration is low, the discharge due to the alkali weight loss tends to be insufficient. In addition, if the alkali concentration is high or the weight reduction time is lengthened in order to obtain a sharp watermark pattern after sufficient removal, the part that is not printed with the paste will also dissolve due to the alkali weight loss and the paste will be printed. It was difficult to obtain a sharp watermark pattern in which the target portion was dissolved.
[0007]
An object of the present invention is to solve the above-mentioned problems. The alkali of the polyester fiber in the portion where the paste is printed is compared with the alkali weight loss rate in the portion of the polyester fiber where the paste is not printed. An object of the present invention is to provide a polyester fabric for discharge processing that can obtain a sharp watermark pattern by significantly increasing the weight loss rate.
[0008]
[Means for Solving the Problems]
The gist of the present invention is a paste containing a polyhydric alcohol ethylene oxide adduct obtained by adding 2 mol or more of ethylene oxide to a polyhydric alcohol and a quaternary ammonium salt , wherein the polyhydric alcohol ethylene oxide adduct is 1 per 100 g of the paste. It is in the polyester fabric for the discharge process to which the glue which contains -50g and 0.5-10g of quaternary ammonium salt per 100g of glue adhered.
[0009]
DETAILED DESCRIPTION OF THE INVENTION
It is necessary that the paste fabric containing the polyhydric alcohol ethylene oxide adduct in which 2 mol or more of ethylene oxide is added to the polyhydric alcohol and the quaternary ammonium salt are attached to the polyester fabric for discharge processing of the present invention.
[0010]
In the present invention, by using a paste that uses a polyhydric alcohol ethylene oxide adduct and a quaternary ammonium salt in combination, it is possible to promote weight reduction of the portion to which the paste is attached, and to obtain a sharp watermark pattern. .
[0011]
Examples of the polyhydric alcohol ethylene oxide adduct of the present invention include ethylene glycol, propylene glycol, hydrobenzoin, benzopinacol, dihydric alcohols such as cyclopentane-1,2-diol and cyclohexane-1,4-diol, and three such as glycerin. A product obtained by adding 2 mol or more of ethylene oxide to a monohydric alcohol is used.
[0012]
Examples of the polyhydric alcohol ethylene oxide adduct preferably used in the present invention include an ethylene oxide 5-30 mol adduct of ethylene glycol and an ethylene oxide 3-28 mol adduct of glycerin.
[0013]
The quaternary ammonium salt is not particularly limited as long as it has an effect of promoting alkali weight loss on the polyester fiber, but in particular, [RN (CH 2 C 6 H 5 ) (CH 2 CH 2 O) mH) (CH 2 CH 2 O) nH)] + Cl (wherein R is an alkyl group having 12 to 18 carbon atoms, m + n is a number contained between 2 and 30), one or more quaternary ammonium salts having a structural formula Is preferred. Moreover, when the value of m + n in the formula exceeds 30, the weight loss promoting effect tends to be weakened.
[0014]
In the present invention, the polyhydric alcohol ethylene oxide adduct contains 1 to 50 g, preferably 5 to 20 g, and quaternary ammonium salt is contained in an amount of 0.5 to 10 g, preferably 1 to 3 g, per 100 g of the paste. It is preferable that the agent adheres.
[0015]
If the polyhydric alcohol ethylene oxide adduct is less than 1 g per 100 g of glue, the weight loss promoting effect of the printed part is insufficient, the difference in weight loss between the unexposed part and the unexposed part is small, and it is difficult to obtain a sharp pattern. When the amount exceeds 50 g per 100 g of the agent, the polyhydric alcohol ethylene oxide adduct oozes out to the non-printing portion and the printing pattern becomes unclear.
[0016]
When the amount of the quaternary ammonium salt is less than 0.5 g per 100 g of the paste, the effect of the combined use with the polyhydric alcohol ethylene oxide adduct is insufficient, and it is difficult to obtain the intended sharp pattern.
[0017]
On the other hand, when the amount exceeds 10 g per 100 g of the sizing agent, foaming is likely to occur and workability is likely to deteriorate, and the strength of the fabric after the discharge processing is likely to be reduced.
[0018]
In addition, as a main component of the paste of this invention, wheat flour, tragacanth gum, locust bean gum, carboxymethylcellulose, polyvinyl alcohol, sodium polyacrylate, etc. are mentioned, You may use these individually or in mixture of 2 or more types.
[0019]
Furthermore, the polyester fabric for discharge processing according to the present invention may be a fabric containing polyester fibers, but the modified polyester fibers copolymerized with 1 to 15 mol% of the third component and the third component of 0.5 mol% or less. It is preferable to contain the unmodified polyester fiber in order to obtain a sharp watermark pattern by means of the discharging process.
[0020]
The modified polyester fiber is preferably a polyester fiber modified with a third component having an alkali metal sulfonic acid group, and polyethylene obtained by copolymerizing 5-sodiumsulfoisophthalic acid and an aliphatic dicarboxylic acid such as adipic acid or sebacic acid. Polyester fibers made of terephthalate, particularly preferably polyethylene terephthalate copolymerized with 1.5 to 4 mol% of 5-sodium sulfosophthalic acid and 3 to 13 mol of adipic acid can be mentioned.
[0021]
In addition, although the polyester fabric for a discharge process of this invention is obtained by adhering a paste agent by the arbitrary methods to the fabric containing a polyester-type fiber, the method by a printing is preferable. The printing can be arbitrarily performed by any known method, such as partial printing of a pattern or the like, or printing of the entire surface.
[0022]
Examples of the printing method include flat screen printing, rotary screen printing, roller printing, bigo printing, and ink jet printing.
[0023]
The polyester fabric for removal processing according to the present invention can be treated with an aqueous alkali solution after heat treatment to preferentially reduce the amount of alkali on the portion to which the paste has adhered, thereby obtaining a sharp watermark pattern.
[0024]
The heat treatment temperature needs to be 100 to 200 ° C. If the heat treatment temperature is less than 100 ° C., the weight loss accelerator is not impregnated in the modified polyester, and the weight loss promoting effect is insufficient and a sharp pattern cannot be obtained, and if it exceeds 200 ° C., the texture of the polyester is cured.
[0025]
The heat treatment is performed by dry heat or wet heat, and preferably 30 seconds to 5 minutes for dry heat and 30 seconds to 30 minutes for wet heat.
[0026]
As the alkaline aqueous solution, an aqueous solution of an alkali metal hydroxide such as sodium hydroxide or potassium hydroxide, or an alkaline earth metal hydroxide such as magnesium hydroxide or calcium hydroxide is used. If necessary, triethanolamine, diethanolamine, mono An amine such as ethanolamine may be used in combination.
[0027]
The weight loss conditions with the aqueous alkali solution vary depending on the polymer composition and variety of the polyester fiber, but in the case of the aqueous sodium hydroxide solution, the concentration is 0.3 to 3% by mass, preferably 1.5% by mass or less. The temperature is 80 to 130 ° C., preferably 90 to 105 ° C., and the bath ratio is 1: 5 or more, preferably 1:30 or more.
[0028]
【Example】
Hereinafter, the present invention will be described specifically by way of examples.
[0029]
Example 1
As a modified polyester fiber, an 84 dtex / 48 f triangular section yarn made of a copolymer of 2.25 mol% 5-Na sulfoisophthalic acid and 5 mol% adipic acid was subjected to normal false twisting at a false twist temperature of 160 ° C. As a non-modified polyester fiber, a 22 dtex / 1f round cross-section yarn made only of polyethylene terephthalate was prepared.
[0030]
The unmodified polyester fiber is used alone for the warp, and the weft yarn is obtained by twisting the modified polyester fiber and the unmodified polyester fiber at a twist number of 120 T / M, and the warp density is 120 yarns / 吋 and the weft density is 115 yarns. / A plain weave fabric was created.
[0031]
The following plain fabric is printed with the following paste containing a polyhydric alcohol ethylene oxide adduct obtained by adding 2 mol or more of ethylene oxide to a polyhydric alcohol and a quaternary ammonium salt. A fabric was obtained.
[0032]
The resulting polyester fabric for removal processing was dried at 110 ° C. for 2 minutes and then heat-treated in a dry heat atmosphere at a temperature of 190 ° C. for 2 minutes, and then a 1% aqueous solution of sodium hydroxide with a bath ratio of 1:50, 100 ° C. For 45 minutes, washed, neutralized and dried by a conventional method.
[0033]
In the obtained printed portion of the paste of the plain woven fabric, the modified polyester fiber was completely dissolved and removed by alkali treatment, and a discharge-treated fabric having an extremely sharp watermark pattern at the time of molding was obtained.
[0034]
10 mole adduct ... 10 parts by weight of sizing agent glycerin ethylene oxide [C 12 H 25 N (CH 2 C 6 H 5) (CH 2 CH 2 O) mH) (CH 2 CH 2 O) nH)] + Cl - (Mixed product of m + n = 2-8) ... 2.5 parts by weight Fine Gum G17 (Dye made by Daiichi Kogyo Seiyaku Co., Ltd.) ... 6 parts by weight Water ... 81.5 parts by weight ( Comparative Example 1)
Except for using the paste containing no quaternary ammonium salt as described below, a polyester fabric for removal processing was obtained and subjected to removal processing in the same manner as in Example 1.
[0035]
In the obtained plain woven fabric, the modified polyester fiber in the printing part of the paste was not completely removed, and a sharp watermark pattern was not obtained.
[0036]
Adhesive paste glycerin ethylene oxide 10 mol adduct: 10 parts by weight Fine Gum G17 (paste agent manufactured by Daiichi Kogyo Seiyaku Co., Ltd.): 6 parts by weight Water: 84 parts by weight
【The invention's effect】
A sharp watermark pattern can be obtained from the polyester fabric for removal processing of the present invention by the removal processing by alkali weight loss.

Claims (2)

多価アルコールにエチレンオキシドを2モル以上付加した多価アルコールエチレンオキシド付加物と第四級アンモニウム塩を含有する糊剤であって、多価アルコールエチレンオキシド付加物を糊剤100g当たり1〜50g、第四級アンモニウム塩を糊剤100g当たり0.5〜10g含有する糊剤が付着した抜蝕加工用ポリエステル布帛。A paste containing a polyhydric alcohol ethylene oxide adduct obtained by adding 2 moles or more of ethylene oxide to a polyhydric alcohol and a quaternary ammonium salt , wherein the polyhydric alcohol ethylene oxide adduct is added in an amount of 1 to 50 g per 100 g of the paste. A polyester fabric for discharge processing to which a paste containing 0.5 to 10 g of ammonium salt per 100 g of paste is attached. ポリエステル布帛が、アルカリ金属スルホン酸基を有する第三成分により変性されたポリエステル繊維と未変性ポリエステル繊維を含む布帛である請求項1に記載の抜蝕加工用ポリエステル布帛。 The polyester fabric for discharging according to claim 1, wherein the polyester fabric is a fabric comprising polyester fibers modified with a third component having an alkali metal sulfonic acid group and unmodified polyester fibers.
JP2003143120A 2003-05-21 2003-05-21 Polyester fabric for pitting process Expired - Lifetime JP4443856B2 (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102051806A (en) * 2010-11-19 2011-05-11 志向(中国)集团有限公司 Alkali deweighting treatment method for fabrics

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4906342B2 (en) * 2005-01-14 2012-03-28 セーレン株式会社 Manufacturing method of three-dimensional pattern forming fabric
JP2007146319A (en) * 2005-11-25 2007-06-14 Mitsubishi Rayon Textile Co Ltd Fabric for opal finish and method for producing opal finished fabric
JP6379643B2 (en) * 2014-05-07 2018-08-29 三菱ケミカル株式会社 Modified polyester fiber and its mixed goods

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102051806A (en) * 2010-11-19 2011-05-11 志向(中国)集团有限公司 Alkali deweighting treatment method for fabrics
CN102051806B (en) * 2010-11-19 2012-03-21 志向(中国)集团有限公司 Alkali deweighting treatment method for fabrics

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