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JP6028240B2 - Method of manufacturing form-stabilized apparel product and apparel product manufactured using the same - Google Patents

Method of manufacturing form-stabilized apparel product and apparel product manufactured using the same Download PDF

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JP6028240B2
JP6028240B2 JP2012002675A JP2012002675A JP6028240B2 JP 6028240 B2 JP6028240 B2 JP 6028240B2 JP 2012002675 A JP2012002675 A JP 2012002675A JP 2012002675 A JP2012002675 A JP 2012002675A JP 6028240 B2 JP6028240 B2 JP 6028240B2
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小川 一文
小川  一文
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Description

本発明は、形態安定化されたアパレル製品の製造方法とそれを用いて製造された形態安定化されたアパレル製品に関するものである。さらに詳しくは、アパレル製品の繊維間の接触部が、化学結合を介して互いに結合固定されていることにより形態が安定化されていることを特徴とするアパレル製品とその製造方法に関するものである。 The present invention relates to a method for producing a form-stabilized apparel product and a form-stabilized apparel product produced using the method. More specifically, the present invention relates to an apparel product and a method for producing the apparel product characterized in that the form is stabilized by connecting and fixing contact portions between fibers of the apparel product through chemical bonds.

なお、ここでいうアパレル製品とは、綿、麻、絹、羊毛、アルパカ、アンゴラ、カシミヤ、モヘア等の天然繊維製品、レーヨン・キュプラ・ポリノジック等の再生繊維製品、アセテート・トリアセテート・プロミックス等の半合成繊維製品、ナイロン・ポリエステル・アクリル・ポリ塩化ビニル・ポリウレタン等の合成繊維製品、ガラス・金属等の無機繊維製品や紙製品も含む。 The apparel products mentioned here are natural fiber products such as cotton, hemp, silk, wool, alpaca, Angola, cashmere, mohair, recycled fiber products such as rayon, cupra, polynosic, acetate, triacetate, promix, etc. Semi-synthetic fiber products, synthetic fiber products such as nylon, polyester, acrylic, polyvinyl chloride and polyurethane, inorganic fiber products such as glass and metal, and paper products are also included.

従来技術として、綿の防縮加工には、縮みの原因である綿繊維の不安定な部分を物理的な方法で安定させ、縮みを縦、横ともに1%に留めるサンフォライズ加工がある。また、綿繊維の不安定な部分に樹脂を浸透させて固定し、水を吸収しても繊維が動きにくくして縮みを防ぐ樹脂加工がある。さらに、マイナス33.4度で液化したアンモニア液で、綿繊維を化学的に改質する液体アンモニア加工がある。 As a conventional technique, there is a sun folize processing in which the unstable part of the cotton fiber which is the cause of shrinkage is stabilized by a physical method and the shrinkage is limited to 1% in both length and width. Further, there is a resin processing in which a resin is infiltrated and fixed to an unstable part of cotton fiber, and the fiber hardly moves even if water is absorbed to prevent shrinkage. Furthermore, there is a liquid ammonia process that chemically modifies cotton fibers with an ammonia liquid liquefied at minus 33.4 degrees.

中でも、液体アンモニアを用いた形態安定加工は、ワイシャツや作業服などを洗濯した後、製品に縮みやしわがなく、ノーアイロンで着用できる加工であり、液体アンモニア加工と樹脂加工を施した生地で縫製した後、高温のプレスでセットして形態を安定させる方法(SSP加工)である(特許文献1)。また、縫製した後、製品にホルマリンガスを噴きつけガスを繊維内に浸透させて形態を安定させる方法(VP加工)もある(特許文献2)。 In particular, the form-stabilization process using liquid ammonia is a process that can be worn with no ironing, without shrinking or wrinkling the product after washing shirts and work clothes. After sewing, it is a method (SSP process) which sets with a hot press and stabilizes a form (patent document 1). There is also a method (VP processing) in which formalin gas is injected into a product after sewing and the gas is permeated into the fiber to stabilize the form (Patent Document 2).

特開2003−113579号 公報JP 2003-113579 A 特開平7−316945号 公報Japanese Patent Laid-Open No. 7-316945

しかしながら、いずれの方法も処理前に比べて風合いが著しく悪くなる。また、反応性のガスを用いるため、危険であり、且つ環境面でも負荷が大きく推奨できるものではなかった。 However, the texture of both methods is significantly worse than before processing. Further, since reactive gas is used, it is dangerous and the load is not highly recommended in terms of environment.

以上のような従来技術の欠点に鑑み、本発明は、従来のような反応性のガスを用いることなく、風合いを損なわず、且つ形態安定化されたアパレル製品の製造方法と、それを用いて製造されたアパレル製品を提供することを目的とする。 In view of the drawbacks of the prior art as described above, the present invention provides a method for producing an apparel product that does not impair the texture and uses a reactive gas without using a reactive gas as in the prior art, and uses it. The object is to provide manufactured apparel products.

前記目的を達成するため、具体的に提供される第1の発明は、少なくともアパレル製品の繊維表面を、熱または光熱反応性の官能基(A)と活性水素基と反応する官能基(B)を含む物質と溶媒を含む処理液と接触させて反応させ、前記繊維表面に反応性の有機被膜または反応性の単分子膜を形成する工程と、加熱して前記繊維間の接触部で前記有機被膜を互いに架橋反応させる工程を有することを特徴とする形態安定化されたアパレル製品の製造方法である。 In order to achieve the above object, the first invention specifically provided is a functional group (B) which reacts at least the fiber surface of the apparel product with a thermal or photothermal reactive functional group (A) and an active hydrogen group. And a process of forming a reactive organic film or a reactive monomolecular film on the surface of the fiber, and heating and contacting the organic at the contact portion between the fibers. It is a method for producing a form-stabilized apparel product, comprising a step of cross-linking the coatings with each other.

第2の発明は、第1の発明において、熱または光熱反応性の官能基(A)としてエポキシ基、シンナモイル基、カルコニル基、またはそれらの誘導体基を用いることを特徴とするアパレル製品の製造方法である。 According to a second invention, in the first invention, an epoxy group, a cinnamoyl group, a chalconeyl group, or a derivative group thereof is used as the thermal or photothermal reactive functional group (A). It is.

第3の発明は、第2の発明において、熱または光熱反応性の官能基(A)がエポキシ基、またはそれらの誘導体基であり、空気中で加熱または水蒸気を添加しながら加熱して、前記繊維間の前記反応性の有機被膜接触部では架橋反応させ、前記有機被膜の非接触部では前記有機被膜のエポキシ基、またはそれらの誘導体基を失活させることを特徴とするアパレル製品の製造方法である。 According to a third invention, in the second invention, the heat- or photothermal-reactive functional group (A) is an epoxy group or a derivative group thereof, and is heated in air or while adding water vapor, A method for producing an apparel product, characterized in that a cross-linking reaction is performed at a contact portion between the reactive organic coatings between fibers, and an epoxy group of the organic coating or a derivative group thereof is deactivated at a non-contact portion of the organic coating. It is.

第4の発明は、第1〜3の発明において、繊維表面の有機被膜が熱または光熱反応性の単分子膜であることを特徴とするアパレル製品の製造方法である。
第5の発明は、少なくとも繊維表面が有機被膜で被われており、前記有機被膜が互いに接触する部分で前記繊維が前記被膜を介して互いに結合していることを特徴とする形態安定化されたアパレル製品である。
第6の発明は、第5の発明において、繊維表面の有機被膜が単分子膜であることを特徴とする形態安定化されたアパレル製品である。
A fourth invention is a method for producing an apparel product according to the first to third inventions, wherein the organic coating on the fiber surface is a heat or photothermal reactive monomolecular film.
According to a fifth aspect of the invention, the form is stabilized, wherein at least the fiber surface is covered with an organic coating, and the fibers are bonded to each other through the coating at a portion where the organic coating contacts each other Apparel product.
A sixth invention is a form-stabilized apparel product according to the fifth invention, wherein the organic coating on the fiber surface is a monomolecular film.

以上に説明したように、本発明によれば、アパレル製品の繊維間の繊維同士の接触部が化学結合を介して互いに結合固定されているため、風合いを損なうことがなく、一度のアイロン加工のみで形態安定性に優れたアパレル製品を提供できる効果がある。 As described above, according to the present invention, since the contact portions between the fibers of the apparel product are bonded and fixed to each other through a chemical bond, the texture is not impaired, and only one ironing process is performed. It has the effect of providing apparel products with excellent shape stability.

本発明のアパレル製品の繊維表面が、熱または光熱反応性の単分子膜で被覆されている状況を説明するために、繊維表面を分子レベルまで拡大した断面概念図。The cross-sectional conceptual diagram which expanded the fiber surface to the molecular level, in order to demonstrate the condition where the fiber surface of the apparel product of this invention is coat | covered with the heat | fever or photothermal reactivity monomolecular film. 本発明のアパレル製品の繊維表面が、繊維間の接触部で二つの固定された分子を介して架橋されている状況を説明するために、繊維接触部の表面を分子レベルまで拡大した断面概念図。The cross-sectional conceptual diagram which expanded the surface of the fiber contact part to the molecular level in order to explain the situation where the fiber surface of the apparel product of the present invention is cross-linked via two fixed molecules at the contact part between the fibers . (a)は、アイロンかけ直後、(b)は、通常の洗濯を50回行った後の繊維の形態安定性を示す写真。(A) is a photograph showing the morphological stability of the fiber immediately after ironing, and (b) after 50 regular washings.

本発明は、形態安定性に優れた撥水撥油防汚性アパレル製品とその製造方法を提供するものである。 The present invention provides a water and oil repellent antifouling apparel product excellent in form stability and a method for producing the same.

少なくともアパレル製品の繊維表面を、熱または光熱反応性の官能基(A)と活性水素基と反応する官能基(B)を含む物質と溶媒を含む処理液と接触させて反応させ、前記繊維表面に反応性の有機被膜(単分子膜)を形成する工程と、加熱して前記繊維間の接触部で前記有機被膜を互いに架橋反応させる工程を用いて、少なくとも繊維表面が有機被膜で被われており、前記有機被膜が互いに接触する部分で前記繊維が前記被膜を介して互いに結合していることを特徴とする形態安定化されたアパレル製品を提供する。 At least the fiber surface of the apparel product is brought into contact with a treatment liquid containing a solvent and a substance containing a functional group (B) that reacts with a thermal or photothermal reactive functional group (A) and an active hydrogen group, and the fiber surface At least the fiber surface is covered with an organic coating using a step of forming a reactive organic coating (monomolecular film) and a step of crosslinking the organic coating to each other at a contact portion between the fibers by heating. In addition, the present invention provides a form-stabilized apparel product characterized in that the fibers are bonded to each other through the coating at portions where the organic coatings are in contact with each other.

前記製造方法によれば、アパレル製品の繊維間の繊維同士の接触部が化学結合を介して互いに結合固定されているため、風合いを損なうことがなく、一度のアイロン加工のみで形態安定性に優れたアパレル製品を提供できる作用がある。 According to the manufacturing method, since the contact portion between the fibers of the apparel product is bonded and fixed to each other through a chemical bond, the texture is not impaired, and the form stability is excellent only by one ironing process. There is an effect that can provide apparel products.

さらに、加熱の際、非接触部では、反応性の官能基は失活されるので、製品を着用したとき不都合が生じることは全くない。 Furthermore, since the reactive functional group is deactivated in the non-contact part during heating, there is no inconvenience when the product is worn.

次に、本発明の作用効果を確認するために行った実施例を説明する。なお、これらの実施例は、単なる例示であり、本発明を限定するものではない。 Next, examples carried out for confirming the effects of the present invention will be described. In addition, these Examples are only illustrations and do not limit this invention.

まず、熱または光熱反応性の官能基(A)としてのエポキシ基と炭化水素基と活性水素基と反応する官能基(B)としてのアルコキシシリル基を含む物質、例えば、CHOCH(CH2 Si(OA) 3 (ここで、CHOCH−基は、エポキシ基を表し、nは1〜25の整数、Aはアルキル基を表す。)、具体的には、9,10−エポキシデシルトリメトキシシラン(CHOCH(CH2 Si(OA) 3 以下、EDSで表す。)(ここで、CHOCH−基はエポキシ基を表す。))と、非水系の溶媒として、イソパラフィンを用い、0.03mol/Lなるように混合して化学吸着液を調製した。
First, a substance containing an alkoxysilyl group as a functional group (B) that reacts with an epoxy group, a hydrocarbon group, and an active hydrogen group as a thermal or photothermal reactive functional group (A), for example, CH 2 OCH (CH 2 ) N Si (OA) 3 (wherein the CH 2 OCH— group represents an epoxy group, n represents an integer of 1 to 25, and A represents an alkyl group), specifically, 9,10-epoxy. Decyltrimethoxysilane (CH 2 OCH (CH 2 ) 8 Si (OA) 3 or less, represented by EDS (where the CH 2 OCH— group represents an epoxy group)) and a non-aqueous solvent, A chemical adsorption solution was prepared by using isoparaffin and mixing at 0.03 mol / L.

次に、カッターシャツに用いられているポリエステルと綿の混紡(50:50)の布地を用意し、よく洗浄して乾燥した後、空気中で(相対湿度57%、別の実験では70%でも問題なかった。)前記サンプル布地表面にこの溶液を塗布し、1時間程度放置した。 Next, after preparing a polyester / cotton blend (50:50) fabric used in the cutter shirt, washing it thoroughly and drying it, in air (relative humidity 57%, 70% in another experiment) There was no problem.) This solution was applied to the surface of the sample fabric and allowed to stand for about 1 hour.

このとき、イソパラフィン溶媒は大部分蒸発するが、布地のポリエステルや綿繊維1の表面は水酸基が多数含まれているので、前記エポキシ基と炭化水素基とメトキシシリル基を主成分とする物質のメトキシシリル基と表面の水酸基が脱アルコール反応して、繊維1の表面にシロキサン(−SiO−)基2を介して結合したエポキシ基を含む有機被膜を形成できる。そこでさらに、繊維の表面に結合せずに残ったEDSを洗剤を用いて洗浄除去すると、末端にエポキシ基を有する単分子膜3で繊維表面が被覆された布地を製造できた。(図1)
図1において、○は、エポキシ基4を表している。ジグザグ線は、エチレン鎖5を表している。
At this time, most of the isoparaffin solvent evaporates, but since the surface of the polyester or cotton fiber 1 of the fabric contains a large number of hydroxyl groups, methoxy which is a substance mainly composed of the epoxy group, hydrocarbon group and methoxysilyl group. An organic coating containing an epoxy group bonded to the surface of the fiber 1 via a siloxane (—SiO—) group 2 can be formed by a dealcoholization reaction between the silyl group and the surface hydroxyl group. Therefore, when the EDS remaining without being bonded to the fiber surface was removed by washing with a detergent, a fabric in which the fiber surface was coated with the monomolecular film 3 having an epoxy group at the end could be produced. (Figure 1)
In FIG. 1, ◯ represents the epoxy group 4. The zigzag line represents the ethylene chain 5.

このとき、エチレン鎖の炭素数が8以上であれば、エポキシ基4は、繊維表面に大部分露出する。また、前記化学吸着液にシラノール縮合触媒、または酸触媒を0.0003mol/L程度添加しておくと、吸着反応を加速でき、被膜製造時間を短縮できた。   At this time, if the carbon number of the ethylene chain is 8 or more, the epoxy group 4 is mostly exposed on the fiber surface. Further, when a silanol condensation catalyst or an acid catalyst was added to the chemical adsorption solution in an amount of about 0.0003 mol / L, the adsorption reaction could be accelerated and the film production time could be shortened.

次に、アイロンを用いて中温(140〜160℃)でプレスすると、図2に示したように、それぞれの繊維が接触した部分では、エポキシ基がカップリングして繊維間を架橋6した状態となり、形態安定性が発現する。ここで、図3の(a)は、サンプルとして用いた混紡布地をアイロンかけした直後の写真であり、図3の(b)は、通常の洗濯を50回行った後の繊維の形態安定性を示す写真である。   Next, when pressing at an intermediate temperature (140 to 160 ° C.) using an iron, as shown in FIG. 2, at the portion where each fiber is in contact, the epoxy group is coupled and the fibers are cross-linked 6. Morphological stability is manifested. Here, (a) in FIG. 3 is a photograph immediately after ironing the blended fabric used as a sample, and (b) in FIG. 3 is the morphological stability of the fiber after 50 times of normal washing. It is a photograph which shows.

なお、このとき、繊維間の非接触部では、エポキシ基は全て開環して空気中の水分と反応し水酸基に変換され、被膜は1nm程度の膜厚であるので、繊維の風合いは全く損なわれなかった。   At this time, in the non-contact portion between the fibers, all the epoxy groups are ring-opened, react with moisture in the air and converted to hydroxyl groups, and the film has a film thickness of about 1 nm. It wasn't.

ここで、アイロンの温度は、高温(180〜210℃)が良かったが、低温(80〜120℃)でも形態安定加工効果はあった。また、スチームを添加しながらプレスした場合も、同様の結果が得られた。   Here, a high temperature (180 to 210 ° C.) was good for the temperature of the iron, but there was a form-stable processing effect even at a low temperature (80 to 120 ° C.). Similar results were obtained when pressing while adding steam.

また、繊維は、種々試してみたが、綿、麻、絹、羊毛、アルパカ、アンゴラ、カシミヤ、モヘア等の天然繊維製品、レーヨン・キュプラ・ポリノジック等の再生繊維製品、アセテート・トリアセテート・プロミックス等の半合成繊維製品、ナイロン・ポリエステル・アクリル・ポリ塩化ビニル・ポリウレタン等の合成繊維製品、ガラス・金属等の無機繊維製品や紙製品で同様の効果が確かめられた。 In addition, we tried various kinds of fibers, but natural fiber products such as cotton, hemp, silk, wool, alpaca, Angola, cashmere, mohair, regenerated fiber products such as rayon, cupra, polynosic, acetate, triacetate, promix, etc. The same effects were confirmed in semi-synthetic fiber products, synthetic fiber products such as nylon, polyester, acrylic, polyvinyl chloride and polyurethane, inorganic fiber products such as glass and metal, and paper products.

また、前期実施例では、化学吸着溶液の溶媒としてイソパラフィン(非水系の有機溶媒なら、パラフィン系や、フッ素系の溶媒でも同様であった。)を用いたが、エタノールやテトラアルキルアンモニウム塩の様な界面活性剤(分散剤)を含む水系溶媒を用いても同様に製造可能であった。   In the previous examples, isoparaffin (a non-aqueous organic solvent was the same with a paraffin or a fluorinated solvent) was used as the solvent for the chemisorption solution. Even when an aqueous solvent containing a surfactant (dispersant) was used, it could be produced in the same manner.

さらにまた、熱または光熱反応性の官能基(A)としてエポキシ基、シンナモイル基、カルコニル基、またはそれらの誘導体基を用いても同様の結果が得られた。 Furthermore, similar results were obtained when an epoxy group, a cinnamoyl group, a chalconyl group, or a derivative group thereof was used as the thermal or photothermal reactive functional group (A).

1 繊維表面
2 シロキサン基
3,3’ 反応性の単分子膜
4 反応性の官能基(エポキシ基)
5 反応性の官能基(エポキシ基)がカップリングして架橋した状態
DESCRIPTION OF SYMBOLS 1 Fiber surface 2 Siloxane group 3,3 'Reactive monomolecular film 4 Reactive functional group (epoxy group)
5 Reactive functional groups (epoxy groups) coupled and crosslinked

Claims (2)

少なくともアパレル製品の繊維表面を、熱または光熱反応性の官能基(A)と活性水素基と反応する官能基(B)を含む物質と溶媒を含む処理液と接触させて反応させ、前記繊維表面に、末端に前記熱または光熱反応性の官能基(A)を有する有機被膜または単分子膜を形成する工程と、加熱して前記繊維間の接触部で前記有機被膜または単分子膜を互いに架橋反応させる工程を有する形態安定化されたアパレル製品の製造方法において、前記熱または光熱反応性の官能基(A)がエポキシ基であり、加熱または水蒸気を添加しながら加熱して、前記繊維間の有機被膜または単分子膜の接触部では前記エポキシ基同士を架橋反応させ、前記有機被膜または単分子膜の非接触部では前記エポキシ基を失活させることを特徴とする形態安定化されたアパレル製品の製造方法。 At least the fiber surface of the apparel product is brought into contact with a treatment liquid containing a solvent and a substance containing a functional group (B) that reacts with a thermal or photothermal reactive functional group (A) and an active hydrogen group, and the fiber surface And a step of forming an organic film or monomolecular film having the thermal or photothermal reactive functional group (A) at the terminal, and heating to cross-link the organic film or monomolecular film at the contact portion between the fibers. In the method for producing a form-stabilized apparel product having a step of reacting , the heat- or photothermal-reactive functional group (A) is an epoxy group, and heating or heating while adding water vapor is performed between the fibers. the contact portion of the organic coating or monolayer by crosslinking the epoxy groups to each other, wherein the non-contact portion of the organic coating or monolayer is form stabilized, characterized in that to deactivate the epoxy groups Method of manufacturing the apparel products. 少なくとも繊維表面に、末端にエポキシ基を有する単分子膜が形成されており、前記エポキシ基同士がカップリングして繊維間が結合していることを特徴とする形態安定化されたアパレル製品。

A form-stabilized apparel product , wherein a monomolecular film having an epoxy group at a terminal is formed at least on the surface of a fiber , and the epoxy groups are coupled to each other so that fibers are bonded to each other .

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