JP2009068145A - Method for modifying fiber or fiber product and apparatus therefor - Google Patents

Method for modifying fiber or fiber product and apparatus therefor Download PDF

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JP2009068145A
JP2009068145A JP2007238545A JP2007238545A JP2009068145A JP 2009068145 A JP2009068145 A JP 2009068145A JP 2007238545 A JP2007238545 A JP 2007238545A JP 2007238545 A JP2007238545 A JP 2007238545A JP 2009068145 A JP2009068145 A JP 2009068145A
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fiber
fibers
carbon
compound
light
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JP5263752B2 (en
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Akihiko Oouchi
秋比古 大内
Mitsuo Sobashima
光郎 傍島
Akichika Sahashi
晃周 佐橋
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Nisshinbo Holdings Inc
National Institute of Advanced Industrial Science and Technology AIST
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National Institute of Advanced Industrial Science and Technology AIST
Nisshinbo Industries Inc
Nisshin Spinning Co Ltd
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Abstract

<P>PROBLEM TO BE SOLVED: To provide a method for modifying fibers or a fiber product, by which the dyeability or the like of the fibers or a fiber product containing cellulosic fibers or animal fibers can safely be modified in a simple operation at room temperature to save energy, and to provide an apparatus therefor. <P>SOLUTION: This method for modifying the fibers or fiber product containing the cellulosic fibers or animal fibers includes irradiating the fibers or fiber product containing the cellulosic fibers or animal fibers with light in the presence of a compound producing a radical by the irradiation with light and a compound having a carbon-carbon double bond in which an electron-attracting group is directly bound to carbon atoms having the double bond, or the method for modifying the fibers or fiber product containing the cellulosic fibers or animal fibers includes irradiating the fibers or fiber product containing the cellulosic fibers or animal fibers with light in the presence of a compound producing a radical by the irradiation with light and then being treated with a compound having a carbon-carbon double bond in which an electron-attracting group is directly bound to carbon atoms having the double bond. The compound producing the radical by the irradiation with light is preferably a peroxide. The method also includes an embodiment that the fibers or fiber product is treated with a reducing agent after the irradiation with light. <P>COPYRIGHT: (C)2009,JPO&INPIT

Description

本発明は、セルロース系繊維又は動物性繊維を含む、繊維又は繊維製品の改質方法とこれを実施するための装置に関するものである。   The present invention relates to a method for modifying a fiber or a fiber product including cellulosic fibers or animal fibers, and an apparatus for carrying out the method.

現在、セルロース系繊維又は動物性繊維を含む混紡繊維等は、衣料品等の原料として広く大量に用いられている。これらの繊維製品では、一般に、原料自体に不足している染色加工性等の性能を付与するための改質がなされている(例えば、非特許文献1、2、3参照)。   Currently, blended fibers including cellulosic fibers or animal fibers are widely used in large quantities as raw materials for clothing and the like. These fiber products are generally modified to impart performances such as dyeing processability that are lacking in the raw materials themselves (see, for example, Non-Patent Documents 1, 2, and 3).

しかし、これらの改質の多くは高温処理により行われているため、大量のエネルギーを要する多消費型プロセスとなっており、多量の二酸化炭素の放出を伴い、また、装置を始動してからの温度が高温で安定する迄に長時間要し、その間に無駄なエネルギーを要するという問題があった。   However, since many of these reforms are performed by high-temperature treatment, it is a multi-consumption type process that requires a large amount of energy, which involves the release of a large amount of carbon dioxide. There was a problem that it took a long time for the temperature to stabilize at a high temperature, and wasteful energy was required during that time.

また、これらの改質法では各種樹脂類、塩類、金属類、有機化合物などの機能性物質を物理的に付与することが多いため、長期間の使用や洗浄等により機能性物質が繊維や繊維製品から脱離し、その効果が十分に発現しないという問題もあった。   Also, these modification methods often physically apply functional substances such as various resins, salts, metals, organic compounds, etc., so that the functional substances may become fibers or fibers after long-term use or washing. There was also a problem that it was detached from the product and the effect was not fully exhibited.

そのため、繊維に対する化学反応により改質して機能付与することも行われているが、この化学反応は通常高温処理やプラズマや電子線等の物理的手段により行われる場合が多く、いずれの場合もエネルギー多消費型プロセスとなり、また大型の装置や高真空等の特殊な条件も時には必要とするといった難点があった。   For this reason, it is also carried out by modifying and imparting a function by a chemical reaction to the fiber, but this chemical reaction is usually carried out by physical means such as high temperature treatment or plasma or electron beam, and in any case This is an energy intensive process, and there are also disadvantages that special conditions such as large equipment and high vacuum are sometimes required.

そして、ここで用いられる化学反応により行われたセルロース系繊維又は動物性繊維を含む、または該繊維を含む繊維、及び該繊維または該繊維を含む繊維からなる繊維製品の改質は多くの場合加水分解により失われ、その為洗濯等により徐々に機能が低下するという問題もあった。
塩澤和男、染色仕上加工技術、地人書館、1991年発行、3.5, 3.7〜3.9、3.12節、及び第6、7章 日本学術振興会、繊維・高分子機能加工第120委員会編、学振版染色機能加工要論、色染社、2003年発行、第7、8章 繊維学会編著、やさしい繊維の基礎知識、日刊工業新聞社、2004年発行、第9章
And, in many cases, the modification of a fiber product containing or containing a cellulosic fiber or animal fiber, or a fiber product made of the fiber or the fiber containing the fiber, carried out by a chemical reaction used in this case. There is also a problem that the function is gradually lost due to washing or the like because of loss.
Kazuo Shiozawa, Dyeing Finishing Technology, Jinshokan, 1991, 3.5, 3.7-3.9, Section 3.12, and Chapters 6 and 7 Japan Society for the Promotion of Science, 120th Committee on Textile / Polymer Functional Processing, Gakushinban Dyeing Functional Processing Overview, Color Dyeing Company, 2003, Chapters 7, 8 Edited by Textile Society, Basic knowledge of gentle fibers, published by Nikkan Kogyo Shimbun, 2004, Chapter 9

本発明は、このような問題点を克服するためになされたものであって、省エンルギー型であり、室温でかつ簡便な操作で安全に、セルロース系繊維又は動物性繊維を含む、繊維や繊維製品の改質を容易とする方法およびそのための装置を提供することを目的とする。   The present invention has been made in order to overcome such problems, and is a fiber or fiber that is an energy-saving type and contains cellulosic fibers or animal fibers safely at room temperature and with a simple operation. It is an object of the present invention to provide a method and an apparatus for facilitating product modification.

本発明者らは、かかる従来技術の難点を解消するために鋭意検討した結果、セルロース系繊維又は動物性繊維を含む繊維や繊維製品を、光照射によりラジカルを発生する化合物と電子吸引性基が直接炭素−炭素二重結合に結合した炭素−炭素二重結合を有する化合物の存在下で光照射する方法が極めて有効であることを見出し、この知見に基づき本発明をなすに至った。   As a result of diligent studies to solve the problems of the prior art, the present inventors have found that a fiber or a fiber product containing cellulosic fibers or animal fibers contains a compound that generates radicals by light irradiation and an electron-withdrawing group. It has been found that a method of irradiating light in the presence of a compound having a carbon-carbon double bond directly bonded to a carbon-carbon double bond is very effective, and the present invention has been made based on this finding.

すなわち、この出願によれば、以下の発明が提供される。
〈1〉光照射によりラジカルを発生する化合物と電子吸引性基が直接炭素−炭素二重結合を形成する炭素原子に結合した炭素−炭素二重結合を有する化合物の存在下、セルロース系繊維(アスペクト比が300以下で、その存在比が全体の60%以上のセルロース系繊維を除く)又は動物性繊維を含む、繊維又は繊維製品に対し、光照射することを特徴とする繊維又は繊維製品の改質方法。
〈2〉光照射によりラジカルを発生する化合物の存在下、セルロース系繊維(アスペクト比が300以下で、その存在比が全体の60%以上のセルロース系繊維を除く)又は動物性繊維を含む、繊維又は繊維製品に対し、光照射した後に、前記炭素−炭素二重結合を有する化合物と処理することを特徴とする繊維又は繊維製品の改質方法。
〈3〉光照射によりラジカルを発生する化合物を、セルロース系繊維又は動物性繊維を含む、繊維又は繊維製品の一部だけに付与して光照射することを特徴とする〈1〉又は〈2〉の改質方法。
〈4〉光照射によりラジカルを発生する化合物が過酸化物であることを特徴とする〈1〉から〈3〉のいずれかに記載の改質方法。
〈5〉光ビームまたはマスクを通して光照射を行うことを特徴とする〈1〉〜〈4〉のいずれかに記載の改質方法。
〈6〉上記<1>から<5>のいずれかの方法での光照射後に繊維及び繊維製品を還元剤で処理することを特徴とする繊維及び繊維製品の改質方法。
〈7〉上記<1>、<3>から<6>のいずれかの方法を行うための改質装置であって、光源とともに、光照射によりラジカルを発生する化合物と前記炭素−炭素二重結合を有する化合物の存在下でセルロース系繊維又は動物性繊維を含む、繊維又は繊維製品に光照射する手段を備えている繊維又は繊維製品の改質装置。
〈8〉上記<2>から<6>のいずれかの方法を行うための改質装置であって、光源とともに、光照射によりラジカルを発生する化合物の存在下でセルロース系繊維又は動物性繊維を含む、繊維又は繊維製品に光照射する手段と、光照射した後に該炭素−炭素二重結合を有する化合物と処理する手段を備えている繊維又は繊維製品の改質装置。
That is, according to this application, the following invention is provided.
<1> Cellulose fibers (aspects) in the presence of a compound that generates radicals upon light irradiation and a compound having a carbon-carbon double bond in which an electron-withdrawing group is directly bonded to a carbon atom that forms a carbon-carbon double bond. A fiber or textile product characterized by irradiating light to a fiber or textile product containing animal fibers) or a fiber product containing a ratio of 300 or less and an abundance ratio of 60% or more of cellulosic fibers. Quality method.
<2> Fibers including cellulosic fibers (excluding cellulosic fibers having an aspect ratio of 300 or less and an abundance ratio of 60% or more) or animal fibers in the presence of a compound that generates radicals upon irradiation with light. Alternatively, the fiber or fiber product is treated with the compound having a carbon-carbon double bond after being irradiated with light.
<3> A compound that generates radicals by light irradiation is applied to only a part of a fiber or a fiber product including cellulosic fibers or animal fibers, and is irradiated with light <1> or <2> Reforming method.
<4> The reforming method according to any one of <1> to <3>, wherein the compound that generates radicals by light irradiation is a peroxide.
<5> The modification method according to any one of <1> to <4>, wherein light irradiation is performed through a light beam or a mask.
<6> A method for modifying a fiber and a fiber product, wherein the fiber and the fiber product are treated with a reducing agent after the light irradiation according to any one of the above <1> to <5>.
<7> A reforming apparatus for performing the method according to any one of <1> and <3> to <6>, wherein the compound generates a radical by light irradiation together with a light source and the carbon-carbon double bond. An apparatus for modifying a fiber or fiber product comprising means for irradiating the fiber or fiber product with light in the presence of a compound having cellulosic fibers or animal fibers.
<8> A reformer for performing any one of the above methods <2> to <6>, wherein cellulosic fibers or animal fibers are combined with a light source in the presence of a compound that generates radicals by light irradiation. An apparatus for modifying a fiber or a textile product, comprising: means for irradiating the fiber or textile product with light; and means for treating the compound having a carbon-carbon double bond after the light irradiation.

本発明の方法と装置によれば、セルロース系繊維又は動物性繊維を含む、繊維又は繊維製品の改質を室温で簡便な装置を用いて安全に行うことができ、また、上記繊維及び繊維製品の改質範囲を拡大して新たな機能の発現や染色性の改善等を実現することができる。また、本発明の方法と装置は、持続的な社会の発展に必要な、省資源、省エネルギー、環境負荷低減技術として多いに寄与するものである。   According to the method and apparatus of the present invention, modification of fibers or textile products including cellulosic fibers or animal fibers can be performed safely at room temperature using a simple apparatus, and the fibers and textile products are also described above. It is possible to realize a new function and an improved dyeability by expanding the modification range. In addition, the method and apparatus of the present invention greatly contributes to resource saving, energy saving, and environmental load reduction technologies necessary for sustainable social development.

本発明でいう、セルロース系繊維又は動物性繊維を含む繊維とは、セルロース系繊維単独又は動物性繊維単独の他、それぞれの単独繊維以外の複数の繊維からなる繊維を意味する。ここで、セルロース系繊維又は動物性繊維以外の繊維とは、ポリエステル、ナイロン等の合成繊維、アセテート等の半合成繊維等を指すものとする。   The fiber containing cellulosic fibers or animal fibers referred to in the present invention means a fiber composed of a plurality of fibers other than the individual single fibers in addition to the cellulosic fibers alone or the animal fibers alone. Here, fibers other than cellulosic fibers or animal fibers refer to synthetic fibers such as polyester and nylon, semi-synthetic fibers such as acetate, and the like.

本発明の対象となるセルロース系繊維としては植物繊維や再生繊維が挙げられる。植物繊維としては木綿、麻、竹繊維、バクテリアやその他の原料から得られるナノファイバー等が挙げられ、再生繊維としてはビスコースレーヨン、ポリノジック、スフ、テンセル、キュプラ、等が挙げられるが、これ以外のセルロース系再生繊維も対象となる。また、本発明の対象となる動物性繊維としては絹や羊毛等が挙げられるが、この他にも動物由来の繊維の任意のものを用いることができる。   Examples of cellulosic fibers that are the subject of the present invention include plant fibers and regenerated fibers. Examples of plant fibers include cotton, hemp, bamboo fibers, nanofibers obtained from bacteria and other raw materials, and examples of regenerated fibers include viscose rayon, polynosic, sufu, tencel, cupra, etc. Cellulosic regenerated fibers are also targeted. In addition, examples of animal fibers that are the subject of the present invention include silk and wool. In addition to these, any fibers derived from animals can be used.

セルロース系繊維又は動物性繊維を含む繊維製品としては糸、織物、衣服、各種容器、装飾品等、主にセルロース系繊維又は動物性繊維からなる製品以外にも、他の素材との複合体等からなる製品にもセルロース系繊維又は動物性繊維に由来する繊維が含まれている場合にはこれらの任意のものを用いることができる。   As fiber products containing cellulosic fibers or animal fibers, in addition to products mainly made of cellulosic fibers or animal fibers, composites with other materials, etc. Any of these products may be used when the product made from the above-mentioned products contains fibers derived from cellulosic fibers or animal fibers.

本発明でいう、セルロース系繊維又は動物性繊維を含む繊維又は繊維製品の改質とは、該繊維及び繊維製品が本来有する機能、性能、性質等とは異なる新たな機能、性能、性質等を付与することを意味し、新たな機能、性能、性質等が付与されていれば、本来有する機能、性能、性質等を併せ持っていてもよい。   In the present invention, the modification of fibers or fiber products containing cellulosic fibers or animal fibers refers to new functions, performances, properties, etc. that are different from the functions, performances, properties, etc. inherent to the fibers and fiber products. It means that it is given, and if a new function, performance, property, etc. are given, it may have the function, performance, property, etc. originally possessed.

繊維及び繊維製品の具体的な改質態様としては、染色性、濃色性、深色性、風合い、防縮性、親水性、撥水性、防水性、親油性、形状記憶性、導電性、しわ加工性、防しわ性、難燃性、樹脂加工性、防虫性、妨カビ性、消臭性、加工性、減量加工、グラフト性、架橋、SR性、電磁波シールド性、メッキ性、芳香性、芳香徐放性等が挙げられるが、これらの機能、性質等に限定されるものではなく、該繊維や繊維製品が本来有する機能、性能、性質等とは異なる新たな機能、性能、性質等を付与するものであればよい。   Specific modifications of fibers and textile products include dyeability, darkness, deep color, texture, shrinkage resistance, hydrophilicity, water repellency, waterproofness, lipophilicity, shape memory, conductivity, wrinkles Processability, wrinkle resistance, flame retardancy, resin processability, insect resistance, mold prevention, deodorization, processability, weight loss processing, grafting, cross-linking, SR, electromagnetic wave shielding, plating, aromatic, Examples include, but are not limited to, these functions, properties, etc., and new functions, performances, properties, etc. that are different from the functions, performances, properties, etc. inherent to the fibers and fiber products. What is necessary is just to give.

本発明において用いる照射光としては目的として付与することによる機能、性能、性質や、付与のための効率等を考慮して選択してよいが、一般的には、120〜800nmの、好ましくは190〜600nmの紫外線や可視光(以下、紫外可視光ともいう)を用いることが望ましい。紫外可視光源としては特に制限はなく、連続光でもパルス光でもよく、低圧水銀灯、高圧水銀灯、キセノン灯、ブラックライト、各種LED、各種エキシマランプ等の通常の光源を用いることができるが、これらに限定されるものではなく従来公知の光源を適宜に用いることができる。照射光強度にも特に制限は無いが、紫外可視光の連続光源としては0.1mW〜10kWの光源が適している。   The irradiation light used in the present invention may be selected in consideration of the function, performance, properties, efficiency for application, etc. provided by the purpose, but in general, it is 120 to 800 nm, preferably 190. It is desirable to use ultraviolet light or visible light (hereinafter also referred to as ultraviolet visible light) of ˜600 nm. The UV-visible light source is not particularly limited and may be continuous light or pulsed light, and ordinary light sources such as low-pressure mercury lamp, high-pressure mercury lamp, xenon lamp, black light, various LEDs, and various excimer lamps can be used. It is not limited and a conventionally well-known light source can be used suitably. Although there is no restriction | limiting in particular in irradiation light intensity, as a continuous light source of ultraviolet visible light, a light source of 0.1 mW-10 kW is suitable.

また光源として各種レーザーを用いることができ、レーザー光はパルス光でも連続照射光でもよいが、エキシマレーザー(ArFエキシマレーザー、KrFエキシマレーザー、XeClエキシマレーザー、XeFエキシマレーザー等)、アルゴンイオンレーザー、クリプトンイオンレーザー、YAGレーザーの第2、及び第3高調波等を用いることができるが、これらに限定されるものではなく従来公知のレーザーを適宜に用いることができる。   Various lasers can be used as the light source, and the laser light may be pulsed light or continuous irradiation light, but excimer laser (ArF excimer laser, KrF excimer laser, XeCl excimer laser, XeF excimer laser, etc.), argon ion laser, krypton The second and third harmonics of an ion laser and a YAG laser can be used, but the present invention is not limited to these, and a conventionally known laser can be used as appropriate.

紫外可視レーザー光としては、特別な制約はないが、波長が140〜800nm、好ましくは190〜600nm程度のものを用いることが望ましい。   Although there is no special restriction | limiting as an ultraviolet-visible laser beam, It is desirable to use a wavelength about 140-800 nm, Preferably about 190-600 nm.

レーザー照射光強度にも特に制限は無いが、パルス光では0.1mJ/パルス〜1kJ/パルス、連続光は0.1mW〜10kWの光源が適している。   Although there is no restriction | limiting in particular also in laser irradiation light intensity | strength, 0.1 mJ / pulse-1 kJ / pulse is suitable for pulsed light, and 0.1 mW-10 kW light source is suitable for continuous light.

光照射には光ビームを用いることができる。このような光ビームとしては各種レーザーの使用が適しているが、通常の光源を用いて各種レンズやミラー類等の光学系を用いて光を特定の方向に照射できるものであればビームが平行光線でなくても用いることができる。これらの光ビームを各種ミラー類等の光学系を用いることにより移動しながら対象となるセルロース系繊維又は動物性繊維を含む、繊維または繊維製品に照射することができる。   A light beam can be used for light irradiation. As such a light beam, use of various lasers is suitable. However, if an ordinary light source can be used to irradiate light in a specific direction using various optical systems such as lenses and mirrors, the beams are parallel. Even if it is not a light beam, it can be used. By moving these light beams by using an optical system such as various mirrors, it is possible to irradiate a fiber or a fiber product including a target cellulosic fiber or animal fiber.

また、マスクを通して光照射を行うこともできる。マスクを用いて光照射を行う場合には、マスクは光源と対象となるセルロース系繊維又は動物性繊維を含む、繊維または繊維製品の間の何れの位置に置いても良く、光源としては上記の光源の何れをも用いることができる。また、光源とマスクの間、及び/又はマスクと対象となるセルロース系繊維又は動物性繊維を含む、繊維または繊維製品の間に各種レンズやミラー類等の光学系を設置して、マスクのパターンを縮小、拡大、変形することもできる。   Moreover, light irradiation can also be performed through a mask. When light irradiation is performed using a mask, the mask may be placed at any position between a light source and a target fiber or fiber product including cellulosic fibers or animal fibers. Any of the light sources can be used. In addition, an optical system such as various lenses and mirrors is installed between the light source and the mask and / or between the mask and the target cellulosic fiber or animal fiber, or between the fiber or the fiber product, and the mask pattern. Can be reduced, enlarged or deformed.

また、通常の光照射、光ビームによる光照射、及びマスクを用いる光照射において、光源の特性、及び/又は各種レンズやミラー類等の光学系を用いることにより光照射面内の光強度に強弱を付けることによりセルロース系繊維又は動物性繊維を含む、繊維または繊維製品の改質の度合いにグラデーションを付けることもできる。   Also, in normal light irradiation, light irradiation with a light beam, and light irradiation using a mask, the intensity of the light in the light irradiation surface is enhanced by using the characteristics of the light source and / or optical systems such as various lenses and mirrors. It is also possible to add gradation to the degree of modification of fibers or fiber products including cellulosic fibers or animal fibers.

光照射時間は、布の種類、厚さ、形態、溶液の種類と濃度、更には、照射紫外可視光の種類や光強度等を考慮することにより適宜定められるが、定常光源の場合は通常1秒〜120分、各種レーザーを用いた場合には連続レーザーでは通常1μ秒〜30分、パルスレーザーでは通常1〜1000パルスもあれば充分であるが、これらの照射時間に関わらず必要な改質が起こるのに必要な時間光照射を行えばよい。   The light irradiation time is appropriately determined by considering the type of cloth, thickness, form, type and concentration of solution, and the type and intensity of irradiated ultraviolet-visible light. When using various lasers, it is usually sufficient to use 1 μsec to 30 minutes for a continuous laser and usually 1 to 1000 pulses for a pulsed laser. Light irradiation may be performed for a time necessary for the occurrence of the above.

本発明において用いる光照射によりラジカルを発生する化合物としては、好ましくは各種過酸化物、各種光重合開始剤、等が挙げられ、特に過酸化水素や過酸類が好ましいが、これらに限定されるものではなく、該化合物が光照射により単独、或いは他の化合物との相互作用により、ラジカル、ラジカルカチオン、或いはラジカルアニオンを発生するものであればよい。   Examples of the compound that generates radicals upon irradiation with light used in the present invention include various peroxides and various photopolymerization initiators, and hydrogen peroxide and peracids are particularly preferable. Instead, it is sufficient that the compound generates radicals, radical cations, or radical anions by light irradiation alone or by interaction with other compounds.

本発明において用いる電子吸引性基が直接炭素−炭素二重結合を形成する炭素原子に結合した炭素−炭素二重結合を有する化合物は芳香族化合物も含み、光照射による繊維及び繊維製品の改質を著しく阻害するものでなければ従来公知の電子吸引性基が直接炭素−炭素二重結合を形成する炭素原子に結合した炭素−炭素二重結合を有する化合物が使用できる。また、該炭素−炭素二重結合が分子内に複数有る化合物、該炭素−炭素二重結合を有する化合物の任意が高分子化合物である化合物、該炭素−炭素二重結合を有する部位が高分子化合物にグラフトされた化合物等も該炭素−炭素二重結合を有する化合物として用いることができる。また、これらの該炭素−炭素二重結合を有する化合物のいずれかを単独で用いてもよいが、複数の該炭素−炭素二重結合を有する化合物からなる混合系を用いることもできる。   The compound having a carbon-carbon double bond in which an electron-withdrawing group used in the present invention is directly bonded to a carbon atom that forms a carbon-carbon double bond includes an aromatic compound, and modification of fibers and fiber products by light irradiation. As long as it does not significantly inhibit the above, a compound having a carbon-carbon double bond in which a conventionally known electron-withdrawing group is bonded to a carbon atom directly forming a carbon-carbon double bond can be used. Further, a compound having a plurality of carbon-carbon double bonds in the molecule, a compound in which any of the compounds having the carbon-carbon double bond is a polymer compound, and a site having the carbon-carbon double bond being a polymer A compound or the like grafted to the compound can also be used as the compound having the carbon-carbon double bond. In addition, any of these compounds having a carbon-carbon double bond may be used alone, but a mixed system composed of a compound having a plurality of the carbon-carbon double bonds may also be used.

ここで用いる電子吸引性基が直接結合した炭素−炭素二重結合の置換基数や置換基の種類にも制限は無く、他の置換基として水素、電子供与性基、電子吸引性基のいずれの特性を有する炭化水素基、各種官能基を有する炭化水素基、各種官能基等、適宜に用いることができる。   There is no limitation on the number of substituents and the type of substituents of the carbon-carbon double bond to which the electron-withdrawing group is directly bonded, and any other substituents such as hydrogen, electron-donating group, and electron-withdrawing group can be used. A hydrocarbon group having characteristics, a hydrocarbon group having various functional groups, various functional groups, and the like can be used as appropriate.

電子吸引性基としては、たとえば、NR 、SR 、NH 、NO、SOR、CN、SOAr、COOH、F、Cl、Br、I、OAr、COOR、OR、COR、SH、SR、OH、Ar、アルキン、アルケン(ここでArは芳香族基を表す)等が挙げられる(非特許文献4参照)が、これらに限定されるものではない。
J. March著、Advanced Organic Chemistry, 4th Ed, John Wiley & Sons, New York, 1992, pp. 17-19 電子吸引性基が直接炭素−炭素二重結合を形成する炭素原子に結合した炭素−炭素二重結合を有する化合物としては、アクリル酸やメタクリル酸等の炭素−炭素二重結合と共役したカルボン酸類、およびこれらのカルボン酸の各種エステルやアミド、アクリロニトリル、フマロニトリル等の炭素−炭素二重結合と共役したニトリル類、ビニルヘキシルエーテル等の各種アルキルエノールエーテル類、メチルビニルケトン、ビタミンK、ビタミンC等の炭素−炭素二重結合と共役したカルボニル化合物類、ニトロエチレン等の炭素−炭素二重結合と共役したニトロオレフィン類、ビニルスルホン酸等の炭素−炭素二重結合と共役したスルホン酸、及びそれらの各種エステル、テストステロン等のステロイド類、スチレン、シクロヘキサジエン、ブタジエン、ヘキサトリエン、各種カロテン、ビタミンA等の共役した炭素−炭素二重結合を有する化合物、フラーレン、アントラセン、等の多核芳香族化合物類、ヒノキチオール等の複数の電子吸引性基が炭素−炭素二重結合と共役したもの、等が挙げられるがこれらに限定されるものではなく、炭素−炭素二重結合に直接電子吸引性基が結合した炭素−炭素二重結合を有する化合物であればよい。また、該炭素−炭素二重結合が分子内に複数有る化合物としては、先に挙げたアラキドン酸等、が挙げられ、該炭素−炭素二重結合を有する化合物が高分子化合物である化合物、該炭素−炭素二重結合を有する部位が高分子化合物にグラフトされた化合物としてはポリビニルアルコールのポリアクリル酸エステルやポリメタクリル酸エステル等が挙げられるが、これらに限定されるものではなく、該炭素−炭素二重結合が分子内に複数有る化合物、該炭素−炭素二重結合を有する化合物が高分子化合物である化合物、該炭素−炭素二重結合を有する部位が高分子化合物にグラフトされた化合物等であればよい。
Examples of the electron-withdrawing group include NR 3 + , SR 2 + , NH 3 + , NO 2 , SO 2 R, CN, SO 2 Ar, COOH, F, Cl, Br, I, OAr, COOR, OR, COR, SH, SR, OH, Ar, alkyne, alkene (where Ar represents an aromatic group) and the like can be mentioned (see Non-Patent Document 4), but are not limited thereto.
J. March, Advanced Organic Chemistry, 4th Ed, John Wiley & Sons, New York, 1992, pp. 17-19 Carbon-carbon with an electron-withdrawing group directly attached to a carbon atom forming a carbon-carbon double bond Examples of the compound having a double bond include carboxylic acids conjugated with carbon-carbon double bonds such as acrylic acid and methacrylic acid, and carbon-carbon double bonds such as various esters, amides, acrylonitrile, and fumaronitrile of these carboxylic acids. Various alkyl enol ethers such as nitriles conjugated with vinyl, hexyl ether, carbonyl compounds conjugated with carbon-carbon double bonds such as methyl vinyl ketone, vitamin K and vitamin C, and carbon-carbon doubles such as nitroethylene Nitroolefins conjugated with bonds, sulfonic acids conjugated with carbon-carbon double bonds such as vinyl sulfonic acid, and various esters thereof Steroids such as testosterone, styrene, cyclohexadiene, butadiene, hexatriene, various carotenes, compounds having conjugated carbon-carbon double bonds such as vitamin A, polynuclear aromatic compounds such as fullerene and anthracene, hinokitiol, etc. Examples include, but are not limited to, those in which a plurality of electron-withdrawing groups are conjugated with a carbon-carbon double bond, etc. Carbon-carbon in which an electron-withdrawing group is directly bonded to the carbon-carbon double bond Any compound having a double bond may be used. Examples of the compound having a plurality of carbon-carbon double bonds in the molecule include arachidonic acid and the like mentioned above, a compound in which the compound having the carbon-carbon double bond is a polymer compound, Examples of the compound in which a site having a carbon-carbon double bond is grafted to a polymer compound include polyacrylic acid ester and polymethacrylic acid ester of polyvinyl alcohol, but are not limited thereto. A compound having a plurality of carbon double bonds in the molecule, a compound in which the compound having the carbon-carbon double bond is a polymer compound, a compound in which a site having the carbon-carbon double bond is grafted to the polymer compound, etc. If it is.

また、本発明においては、改質により付与された新たな機能、性能、性質等の安定化等や、該機能、性能、性質等の更なる改質のために、光照射後に繊維及び繊維製品を還元剤で処理する方法も採ることもできる。   Further, in the present invention, fibers and fiber products after light irradiation are used for stabilization of new functions, performances, properties, etc. imparted by the modification, and for further modifications of the functions, performances, properties, etc. It is also possible to adopt a method of treating with a reducing agent.

還元剤としては、特に制約はなく従来公知の還元剤の任意のものを使用できる。このような還元剤としては、チオ硫酸ナトリウム、ハイドロサルファイト、水素化ホウ素ナトリウム、ロンガリット、亜硫酸ナトリウム、亜硫酸水素ナトリウム、ヒドラジン等、或いは還元性を有するビタミンC、各種アルデヒド類、ギ酸等の有機化合物を挙げることができるが、これらに限定されるものではなく還元性を有するものであればよい。また、これらの還元剤のいずれかを単独で用いてもよいが、複数の還元剤からなる混合物を用いることもできる
本発明の光照射によりラジカルを発生する化合物と電子吸引性基が直接炭素−炭素二重結合を形成する炭素原子に結合した炭素−炭素二重結合を有する化合物の、繊維又は繊維製品に対する作用については、光照射により発生したラジカル(ラジカル、ラジカルカチオン、ラジカルアニオン)種により上記繊維または繊維製品の表面上にラジカルが発生し、この様に発生したラジカル種が該炭素−炭素二重結合と反応して結合を形成することにより改質が起こるものと考えられる。あるいは、光照射により発生したラジカル種により、該炭素−炭素二重結合を有する化合物の重合が上記繊維または繊維製品上で起こり、その結果生じた高分子化合物が上記繊維または繊維製品に物理的に付着することにより改質が起こることも考えられる。さらには、光照射により発生したラジカル種により上記繊維または繊維製品にラジカルが発生し、このラジカルと上記繊維または繊維製品で起こった該炭素−炭素二重結合を有する化合物の重合物中の炭素−炭素二重結合との反応により、該炭素−炭素二重結合を有する化合物の重合体を上記繊維または繊維製品にラジカル反応により結合することによる改質も起こるものと考えられる。このようなラジカルの炭素−炭素二重結合への付加反応は、電子吸引性基を有する炭素−炭素二重結合について広く起こることが有機化学的に知られている(例えば、非特許文献5参照)。また、このような炭素−炭素二重結合を分子内に一つ有する化合物ばかりではなく、分子内に複数有する化合物においても同様のラジカル反応が起こると考えることは合理的である。
The reducing agent is not particularly limited and any conventionally known reducing agent can be used. Examples of such reducing agents include sodium thiosulfate, hydrosulfite, sodium borohydride, Rongalite, sodium sulfite, sodium hydrogen sulfite, hydrazine and the like, or organic compounds such as vitamin C having a reducing property, various aldehydes, formic acid, etc. However, the present invention is not limited to these, and any material having reducibility may be used. In addition, any of these reducing agents may be used alone, but a mixture of a plurality of reducing agents can also be used. The compound that generates radicals upon irradiation with light of the present invention and the electron-withdrawing group are directly carbon- Regarding the action of the compound having a carbon-carbon double bond bonded to the carbon atom forming the carbon double bond on the fiber or the fiber product, the above-mentioned action is performed depending on the radical (radical, radical cation, radical anion) species generated by light irradiation. It is considered that the modification occurs when radicals are generated on the surface of the fiber or the fiber product, and the radical species thus generated react with the carbon-carbon double bond to form a bond. Alternatively, polymerization of the compound having a carbon-carbon double bond occurs on the fiber or fiber product due to radical species generated by light irradiation, and the resulting polymer compound is physically added to the fiber or fiber product. It is also conceivable that modification occurs due to adhesion. Furthermore, a radical is generated in the fiber or the fiber product by the radical species generated by light irradiation, and the carbon in the polymer of the compound having the carbon-carbon double bond generated in the fiber or the fiber product is generated. It is considered that modification by bonding a polymer of a compound having a carbon-carbon double bond to the fiber or fiber product by a radical reaction is caused by the reaction with the carbon double bond. It is organically known that such an addition reaction of a radical to a carbon-carbon double bond occurs widely for a carbon-carbon double bond having an electron-withdrawing group (see, for example, Non-Patent Document 5). ). In addition, it is reasonable to consider that the same radical reaction occurs not only in a compound having one carbon-carbon double bond in the molecule but also in a compound having a plurality of carbon-carbon double bonds in the molecule.

しかし、本発明方法では、上記の推定反応機構に関わらず、光照射によりラジカルを発生する化合物の存在下で、セルロース系繊維又は動物性繊維を含む、繊維や繊維製品が光照射を受けることにより改質が起こればよいことは勿論である。
東郷秀雄著、有機フリーラジカルの化学、講談社サイエンティフィック、2001年発行 本発明の実施の態様に特別な制限はないが、好ましい実施の態様としては、セルロース系繊維又は動物性繊維を含む、繊維又は繊維製品を、光照射によりラジカルを発生する化合物と電子吸引性基が直接炭素−炭素二重結合に結合した炭素−炭素二重結合を有する化合物を含む薬液に浸漬或いは懸濁させて光照射する方法、あるいは該薬液に浸して引き上げた所に光照射する方法、もしくは該薬液を上記繊維または繊維製品に塗布、吹きつけ等を行い光照射する方法等が挙げられるが、これらに限定されるものではない。
However, in the method of the present invention, regardless of the estimated reaction mechanism described above, in the presence of a compound that generates radicals by light irradiation, fibers or fiber products including cellulosic fibers or animal fibers are irradiated with light. Of course, it is sufficient that the reforming occurs.
Hideo Togo, Organic Free Radical Chemistry, Kodansha Scientific, published in 2001 There are no particular restrictions on the embodiment of the present invention, but preferred embodiments include fibers containing cellulosic fibers or animal fibers. Or, fiber products are irradiated with light by immersing or suspending them in a chemical solution containing a compound that generates radicals by light irradiation and a compound having a carbon-carbon double bond in which an electron-withdrawing group is directly bonded to the carbon-carbon double bond. Or a method of irradiating the chemical solution with light, or a method of irradiating the chemical solution with the above-mentioned fibers or fiber products by applying, spraying, etc., but is not limited thereto. It is not a thing.

特に該薬液を上記繊維または繊維製品に塗布、吹きつけ等を行う際にはエアーブラシやブラシ類等を用いて上記繊維または繊維製品全体に該薬液を付与するばかりではなく、対象物の一部に付与することにより部分的な改質を起こすことも可能で、この部分的な改質により文字、図表等の形態を有する改質を起こすことができる。また、これらの光照射は上記繊維または繊維製品が静置している状態、或いは移動している状態で行うことができる。   In particular, when applying or spraying the chemical liquid onto the fiber or fiber product, not only applying the chemical liquid to the entire fiber or fiber product using an air brush or brushes, but also part of the object It is also possible to cause partial reforming by applying to, and by this partial reforming, it is possible to cause reforming having a form such as a character, a chart or the like. Moreover, these light irradiation can be performed in the state which the said fiber or textiles left still, or the state which is moving.

光照射によりラジカルを発生する化合物と電子吸引性基が直接炭素−炭素二重結合を形成する炭素原子に結合した炭素−炭素二重結合を有する化合物を含む薬液で同時に処理する代わりに、光照射によりラジカルを発生する化合物で処理した繊維又は繊維製品に光照射を行う操作と、この様に処理した繊維又は繊維製品を該炭素−炭素二重結合を有する化合物と処理する操作を分けて行うこともでき、それぞれの操作において上記同時処理で用いる手法を使用することができる。   Instead of simultaneously treating with a chemical solution containing a compound that generates radicals by light irradiation and a compound having a carbon-carbon double bond in which an electron-withdrawing group is directly bonded to a carbon atom that forms a carbon-carbon double bond, light irradiation is performed. The operation of irradiating the fiber or fiber product treated with the compound that generates radicals by the above and the operation of treating the fiber or fiber product treated in this way with the compound having the carbon-carbon double bond are performed separately. It is also possible to use the technique used in the above simultaneous processing in each operation.

光照射によりラジカルを発生する化合物と電子吸引性基が直接炭素−炭素二重結合を形成する炭素原子に結合した炭素−炭素二重結合を有する化合物はそれらの溶液であってもよく、その場合の溶媒としては、照射光を殆ど吸収しないで光照射による繊維及び繊維製品の改質を著しく阻害するものでなければ特に制約はなく従来公知の溶媒を適宜に使用することができる。   A compound that generates a radical by light irradiation and a compound having a carbon-carbon double bond in which an electron-withdrawing group is directly bonded to a carbon atom that forms a carbon-carbon double bond may be a solution thereof. The solvent is not particularly limited as long as it does not substantially absorb irradiation light and does not significantly inhibit modification of fibers and fiber products by light irradiation, and a conventionally known solvent can be appropriately used.

このような溶媒としては、たとえば、アセトニトリル、ジメチルスルホキシド、ジメチルホルムアミドなどの極性溶媒の他に、デカン、ドデカン、テトラデカン等の脂肪族炭化水素や、トルエン、キシレン等の芳香族炭化水素(分子内に脂肪族基を有する芳香族炭化水素も含む)等の無極性溶媒、プロピルアミン、エチレンジアミン、各種カルボン酸、各種ポリカルボン酸、などのプロトン性溶媒等を挙げることができるが、これらに限定されるものではない。   Examples of such solvents include polar solvents such as acetonitrile, dimethyl sulfoxide, and dimethylformamide, aliphatic hydrocarbons such as decane, dodecane, and tetradecane, and aromatic hydrocarbons such as toluene and xylene (within the molecule). Non-polar solvents such as aromatic hydrocarbons having aliphatic groups), protic solvents such as propylamine, ethylenediamine, various carboxylic acids, various polycarboxylic acids, and the like, but are not limited thereto. It is not a thing.

また、これらの溶媒のいずれかを単独で用いてもよいが、複数の溶媒からなる混合溶媒を用いることもできる。   Any one of these solvents may be used alone, but a mixed solvent composed of a plurality of solvents may be used.

また、光照射によりラジカルを発生する化合物と電子吸引性基が直接炭素−炭素二重結合を形成する炭素原子に結合した炭素−炭素二重結合を有する化合物、あるいはその溶液の繊維及び繊維製品への浸透性を高める為に界面活性剤を共存させることもできる。   In addition, a compound having a carbon-carbon double bond in which a compound that generates radicals by light irradiation and an electron-withdrawing group are directly bonded to a carbon atom that forms a carbon-carbon double bond, or a fiber and a fiber product of the solution In order to increase the permeability of the surfactant, a surfactant may be allowed to coexist.

界面活性剤としては、光照射による繊維及び繊維製品の改質を著しく阻害するものでなければ従来公知の界面活性剤の任意のものを使用できる。このような界面活性剤としては、たとえば、高級脂肪酸アルカリ塩、アルキル硫酸塩、アルキルスルホン酸塩、アルキルアリールスルホン酸塩、スルホコハク酸エステル塩などの陰イオン界面活性剤、高級アミンハロゲン酸塩、ハロゲン化アルキルピリジニウム、第四アンモニウム塩などの陽イオン界面活性剤、ポリエチレングリコールアルキルエーテル、ポリエチレングリコール脂肪酸エステル、ソルビタン脂肪酸エステル、脂肪酸モノグリセリドなどの非イオン界面活性剤、アミノ酸などの両性表面活性剤などが例示される。   As the surfactant, any conventionally known surfactant can be used as long as it does not significantly inhibit the modification of fibers and fiber products by light irradiation. Examples of such surfactants include anionic surfactants such as higher fatty acid alkali salts, alkyl sulfates, alkyl sulfonates, alkyl aryl sulfonates, sulfosuccinate esters, higher amine halogenates, halogens, and the like. Illustrative examples include cationic surfactants such as alkyl pyridinium fluoride and quaternary ammonium salts, nonionic surfactants such as polyethylene glycol alkyl ethers, polyethylene glycol fatty acid esters, sorbitan fatty acid esters, and fatty acid monoglycerides, and amphoteric surfactants such as amino acids. Is done.

また、これらの界面活性剤のいずれかを単独で用いてもよいが、複数の界面活性剤からなる混合物を用いることもできる。   Further, any of these surfactants may be used alone, but a mixture of a plurality of surfactants can also be used.

また、それらの界面活性剤の溶液を用いることもできるが、このような溶媒としては、水、アルコール類、鎖状または環状の炭化水素類、エーテル類等の単独溶媒あるいはこれらの混合溶媒が挙げられる。界面活性剤の含有量は溶媒に対する界面活性剤の飽和濃度以下であれば特に制限はないが、好ましくは溶媒に対して、0.0001〜50重量%、より好ましくは0.01〜10重量%とするのが適当である。   A solution of these surfactants can also be used. Examples of such a solvent include water, alcohols, chain or cyclic hydrocarbons, single solvents such as ethers, and mixed solvents thereof. It is done. The surfactant content is not particularly limited as long as it is equal to or lower than the saturation concentration of the surfactant with respect to the solvent, but is preferably 0.0001 to 50% by weight, more preferably 0.01 to 10% by weight, based on the solvent. Is appropriate.

つぎに、本発明方法を実施するための代表的な改質装置の幾つかを以下に例示するが、本装置はこれらに限定されるものではない。   Next, some typical reforming apparatuses for carrying out the method of the present invention are exemplified below, but the present apparatus is not limited to these.

図1の装置は、糸状または織物状の天然繊維を含む繊維や繊維製品を改質するために好ましく用いられる改質装置の一例である。図1の装置は、セルロース系繊維又は動物性繊維繊維を含む、繊維や繊維製品の全体に、薬液槽で光照射によりラジカルを発生する化合物と電子吸引性基が直接炭素−炭素二重結合を形成する炭素原子に結合した炭素−炭素二重結合を有する化合物を付与し、該繊維や繊維製品全体に光照射を行い、その後で洗浄槽に於いて過剰な薬液などを除去するものである。   The apparatus shown in FIG. 1 is an example of a reforming apparatus that is preferably used for modifying fibers or fiber products containing natural fibers in the form of threads or fabrics. The apparatus of FIG. 1 has a carbon-carbon double bond directly formed on a fiber or fiber product including cellulosic fibers or animal fiber fibers, and a compound that generates radicals upon irradiation with light in a chemical solution tank and an electron-withdrawing group. A compound having a carbon-carbon double bond bonded to the carbon atom to be formed is imparted, and the fiber or the entire fiber product is irradiated with light, and then an excessive chemical solution or the like is removed in a washing tank.

この装置によれば、上記繊維または繊維製品を薬液に浸漬し、引き上げた所に光照射することができる。   According to this apparatus, the fiber or the fiber product can be immersed in a chemical solution and irradiated to the place where it is pulled up.

図2の装置は、糸状または織物状のセルロース系繊維又は動物性繊維を含む、繊維や繊維製品の改質するために好ましく用いられる改質装置の他の例である。図2の装置は、セルロース系繊維又は動物性繊維を含む、繊維や繊維製品の全体に、薬液槽で光照射によりラジカルを発生する化合物と電子吸引性基が直接炭素−炭素二重結合を形成する炭素原子に結合した炭素−炭素二重結合を有する化合物を付与し、光ビームにより該繊維や繊維製品の一部に光照射を行い、その後で洗浄槽に於いて過剰な薬液などを除去し、その後、還元処理槽で還元剤によって処理するものである。   The apparatus shown in FIG. 2 is another example of a reforming apparatus that is preferably used for modifying fibers and fiber products including cellulosic fibers or animal fibers in the form of threads or fabrics. In the apparatus of FIG. 2, a compound that generates radicals by light irradiation in a chemical solution tank and an electron-withdrawing group directly forms a carbon-carbon double bond on the entire fiber or fiber product including cellulosic fibers or animal fibers. A compound having a carbon-carbon double bond bonded to a carbon atom is applied, and a light beam is used to irradiate a part of the fiber or fiber product, and then an excess chemical solution is removed in a washing tank. Then, it is treated with a reducing agent in a reduction treatment tank.

この装置によれば、上記繊維または繊維製品を薬液に浸漬し、引き上げた所に光学系を用いて光ビームを動かす光照射を行うことにより、必要な箇所に任意のパターンを伴う改質が可能となる。還元剤で処理することによって、光照射時に発生したカルボニル基や過酸化物などの不安定物質をアルコールなどの安定した化合物に変換することができる。   According to this device, the above-mentioned fiber or textile product is immersed in a chemical solution, and light irradiation is performed by moving the light beam using an optical system at the pulled-up position, so that modification with an arbitrary pattern is possible at a required location. It becomes. By treating with a reducing agent, unstable substances such as carbonyl groups and peroxides generated during light irradiation can be converted into stable compounds such as alcohol.

図3の装置は、糸状または織物状のセルロース系繊維又は動物性繊維を含む、繊維や繊維製品の改質するために好ましく用いられる改質装置の更に他の例である。図3の装置は、光照射によりラジカルを発生する化合物と電子吸引性基が直接炭素−炭素二重結合を形成する炭素原子に結合した炭素−炭素二重結合を有する化合物により満たされている薬液槽に、セルロース系繊維又は動物性繊維を含む、繊維や繊維製品を投入し、該薬液と繊維や繊維製品を撹拌しながら光照射を行ものである。   The apparatus shown in FIG. 3 is still another example of a reforming apparatus that is preferably used for modifying fibers and fiber products, including cellulosic fibers or animal fibers in the form of threads or fabrics. The apparatus of FIG. 3 is a chemical solution filled with a compound that generates radicals upon light irradiation and a compound having a carbon-carbon double bond in which an electron-withdrawing group is directly bonded to a carbon atom that forms a carbon-carbon double bond. Fibers or fiber products containing cellulosic fibers or animal fibers are introduced into the tank, and light irradiation is performed while stirring the chemical solution and the fibers or fiber products.

この装置によれば、上記繊維または繊維製品を薬液に浸漬し、必要に応じ薬液を注入しながら撹拌中で光照射を行うことにより、取り扱いが煩雑な小さな上記繊維または繊維製品の改質を容易とする。   According to this apparatus, it is easy to modify the above-mentioned small fiber or fiber product, which is difficult to handle, by immersing the fiber or fiber product in a chemical solution and performing light irradiation while stirring while injecting the chemical solution as necessary. And

図4の装置は、織物状又は成形されたセルロース系繊維又は動物性繊維を含む、繊維や繊維製品の改質するために好ましく用いられる改質装置例である。図4の装置は、セルロース系繊維又は動物性繊維を含む、繊維や繊維製品の一部にスプレー等により光照射によりラジカルを発生する化合物を部分的に付与し、光ビームにより該繊維や繊維製品の一部に光照射を行い、その後で洗浄槽に於いて過剰な薬液などを除去した後、薬液槽で電子吸引性基が直接炭素−炭素二重結合を形成する炭素原子に結合した炭素−炭素二重結合を有する化合物による処理を行うものである。   The apparatus shown in FIG. 4 is an example of a reforming apparatus that is preferably used for modifying fibers and textile products including woven or molded cellulosic fibers or animal fibers. The apparatus of FIG. 4 partially imparts a compound that generates radicals by light irradiation by spraying or the like to a part of the fiber or fiber product including cellulosic fiber or animal fiber, and the fiber or fiber product by a light beam. A portion of the substrate is irradiated with light, and then the excess chemical solution is removed in the washing tank, and then in the chemical solution tank, the electron-withdrawing group is directly bonded to the carbon atom forming the carbon-carbon double bond. Treatment with a compound having a carbon double bond is performed.

この装置によれば、薬液を対象とする上記繊維または繊維製品に吹き付けてから光照射を行うため、光照射によりラジカルを発生する化合物の吹きつけにロボットアーム等の可動機能を付与することにより上記繊維または繊維製品の形態に関係なく必要な箇所に薬液を付与することができ、また、三次元的な光照射の制御を行うことにより、上記繊維または繊維製品の形態に関係なく必要な箇所の改質が可能となる。   According to this apparatus, in order to perform light irradiation after spraying the above-mentioned fiber or fiber product targeted for a chemical solution, the above-mentioned function is given by adding a movable function such as a robot arm to spraying a compound that generates radicals by light irradiation. A chemical solution can be applied to a necessary place regardless of the form of the fiber or the fiber product, and by controlling the three-dimensional light irradiation, the necessary place can be obtained regardless of the form of the fiber or the fiber product. Modification is possible.

次に実施例に基づき、本発明を更に詳細に説明する。もちろん、以下の例によって本発明で限定されることはない。
実施例1
綿布を3mol/Lのアクリル酸と5%の過酸化水素を含む水溶液に含浸させ、引き上げた所に15Wの低圧水銀灯照射を60分行い、水、メタノール、水、中性洗剤、水の順で洗浄した後、一晩減圧乾燥した。得られた布を鑑別染料(カヤスティン)により染色したところ、未処理の綿布と比べて顕著な赤紫色を示したことより、綿布の表面構造が変化し綿布の改質が起きたことが判明した。
実施例2
綿布を0.9mol/Lのメタクリル酸と5%の過酸化水素を含む水溶液に含浸させ、引き上げた所に15Wの低圧水銀灯照射を60分行い、水、メタノール、水、中性洗剤、水の順で洗浄した後、一晩減圧乾燥した。得られた布を鑑別染料(カヤスティン)により染色したところ、未処理の綿布と比べて顕著な青紫色を示したことより、綿布の表面構造が変化し綿布の改質が起きたことが判明した。青紫色は光照射面の方が顕著であった。
実施例3
マーセル化した綿布を3mol/Lのアクリル酸と5%の過酸化水素を含む水溶液に含浸させ、引き上げた所に15Wの低圧水銀灯照射を60分行い、水、メタノール、水、中性洗剤、水の順で洗浄した後、一晩減圧乾燥した。得られた布を鑑別染料(カヤスティン)により染色したところ、未処理の綿布と比べて顕著な赤紫色を示したことより、綿布の表面構造が変化し綿布の改質が起きたことが判明した。赤紫色の度合いは通常の綿布よりも顕著であった。
実施例4
マーセル化した綿布を0.9mol/Lのメタクリル酸と5%の過酸化水素を含む水溶液に含浸させ、引き上げた所に15Wの低圧水銀灯照射を60分行い、水、メタノール、水、中性洗剤、水の順で洗浄した後、一晩減圧乾燥した。得られた布を鑑別染料(カヤスティン)により染色したところ、未処理の綿布と比べて顕著な青紫色を示したことより、綿布の表面構造が変化し綿布の改質が起きたことが判明した。青紫色は光照射面の方が顕著であった。青紫色の度合いは通常の綿布よりも顕著であった。
実施例5
テンセル布を3mol/Lのアクリル酸と5%の過酸化水素を含む水溶液に含浸させ、引き上げた所に15Wの低圧水銀灯照射を60分行い、水、メタノール、水、中性洗剤、水の順で洗浄した後、一晩減圧乾燥した。得られた布を鑑別染料(カヤスティン)により染色したところ、未処理のテンセル布と比べて顕著な赤紫色を示したことより、テンセルの表面構造が変化しテンセル布の改質が起きたことが判明した。
実施例6
テンセル布を0.9mol/Lのメタクリル酸と5%の過酸化水素を含む水溶液に含浸させ、引き上げた所に15Wの低圧水銀灯照射を60分行い、水、メタノール、水、中性洗剤、水の順で洗浄した後、一晩減圧乾燥した。得られた布を鑑別染料(カヤスティン)により染色したところ、未処理のテンセル布と比べて顕著な青紫色を示したことより、テンセルの表面構造が変化しテンセル布の改質が起きたことが判明した。青紫色は光照射面の方が顕著であった。
実施例7
テンセル布を0.3mol/Lのマレイン酸と5%の過酸化水素を含む水溶液に含浸させ、引き上げた所に15Wの低圧水銀灯照射を60分行い、水、メタノール、水、中性洗剤、水の順で洗浄した後、一晩減圧乾燥した。得られた布を鑑別染料(カヤスティン)により染色したところ、未処理のテンセル布と比べて僅かに緑がかった色となったことより、テンセルの表面構造が変化しテンセル布の改質が起きたことが判明した。
実施例8
ポリノジック布を3mol/Lのアクリル酸と5%の過酸化水素を含む水溶液に含浸させ、引き上げた所に15Wの低圧水銀灯照射を60分行い、水、メタノール、水、中性洗剤、水の順で洗浄した後、一晩減圧乾燥した。得られた布を鑑別染料(カヤスティン)により染色したところ、未処理のポリノジック布と比べて顕著な赤紫色を示したことより、ポリノジックの表面構造が変化しポリノジック布の改質が起きたことが判明した。赤紫色は光照射面の方が顕著であった。
実施例9
ポリノジック布を0.9mol/Lのメタクリル酸と5%の過酸化水素を含む水溶液に含浸させ、引き上げた所に15Wの低圧水銀灯照射を60分行い、水、メタノール、水、中性洗剤、水の順で洗浄した後、一晩減圧乾燥した。得られた布を鑑別染料(カヤスティン)により染色したところ、未処理のポリノジック布と比べて顕著な青紫色を示したことより、ポリノジックの表面構造が変化しポリノジック布の改質が起きたことが判明した。青紫色は光照射面の方が顕著であった。
実施例10
ポリノジック布を0.3mol/Lのマレイン酸と5%の過酸化水素を含む水溶液に含浸させ、引き上げた所に15Wの低圧水銀灯照射を60分行い、水、メタノール、水、中性洗剤、水の順で洗浄した後、一晩減圧乾燥した。得られた布を鑑別染料(カヤスティン)により染色したところ、未処理のポリノジック布と比べてやや緑がかった青となったことより、ポリノジックの表面構造が変化し、ポリノジック布の改質が起きたことが判明した。
実施例11
キュプラ布を3mol/Lのアクリル酸と5%の過酸化水素を含む水溶液に含浸させ、引き上げた所に15Wの低圧水銀灯照射を60分行い、水、メタノール、水、中性洗剤、水の順で洗浄した後、一晩減圧乾燥した。得られた布を鑑別染料(カヤスティン)により染色したところ、未処理のキュプラ布と比べて顕著な赤紫色を示したことより、キュプラの表面構造が変化しキュプラ布の改質が起きたことが判明した。
実施例12
キュプラ布を0.9mol/Lのメタクリル酸と5%の過酸化水素を含む水溶液に含浸させ、引き上げた所に15Wの低圧水銀灯照射を60分行い、水、メタノール、水、中性洗剤、水の順で洗浄した後、一晩減圧乾燥した。得られた布を鑑別染料(カヤスティン)により染色したところ、未処理のキュプラ布と比べて顕著な青紫色を示したことより、キュプラの表面構造が変化しキュプラ布の改質が起きたことが判明した。
実施例13
キュプラ布を0.3mol/Lのマレイン酸と5%の過酸化水素を含む水溶液に含浸させ、引き上げた所に15Wの低圧水銀灯照射を60分行い、水、メタノール、水、中性洗剤、水の順で洗浄した後、一晩減圧乾燥した。得られた布を鑑別染料(カヤスティン)により染色したところ、未処理のキュプラ布と比べ濃色化したことより、キュプラの表面構造が変化しキュプラ布の改質が起きたことが判明した。
Next, based on an Example, this invention is demonstrated still in detail. Of course, the present invention is not limited by the following examples.
Example 1
A cotton cloth is impregnated with an aqueous solution containing 3 mol / L acrylic acid and 5% hydrogen peroxide, and a 15 W low-pressure mercury lamp is irradiated for 60 minutes to the pulled-up place, followed by water, methanol, water, neutral detergent, and water in this order. After washing, it was dried overnight under reduced pressure. When the obtained cloth was dyed with a differential dye (Kayastin), it showed a remarkable red-purple color compared to the untreated cotton cloth, indicating that the surface structure of the cotton cloth changed and the cotton cloth was modified. .
Example 2
A cotton cloth is impregnated with an aqueous solution containing 0.9 mol / L methacrylic acid and 5% hydrogen peroxide, and the pulled-up place is irradiated with a 15 W low-pressure mercury lamp for 60 minutes. Water, methanol, water, neutral detergent, water After washing in order, it was dried under reduced pressure overnight. When the obtained cloth was dyed with a differential dye (Kayastin), it showed that the surface structure of the cotton cloth was changed and the cotton cloth was modified due to the remarkable blue-purple color compared to the untreated cotton cloth. . The blue-violet color was more noticeable on the light-irradiated surface.
Example 3
A mercerized cotton cloth is impregnated with an aqueous solution containing 3 mol / L acrylic acid and 5% hydrogen peroxide, and the pulled-up place is irradiated with a 15 W low-pressure mercury lamp for 60 minutes, water, methanol, water, neutral detergent, water After washing in this order, it was dried under reduced pressure overnight. When the obtained cloth was dyed with a differential dye (Kayastin), it showed a remarkable red-purple color compared to the untreated cotton cloth, indicating that the surface structure of the cotton cloth changed and the cotton cloth was modified. . The degree of reddish purple was more prominent than normal cotton cloth.
Example 4
A mercerized cotton cloth is impregnated with an aqueous solution containing 0.9 mol / L methacrylic acid and 5% hydrogen peroxide, and the pulled-up place is irradiated with a 15 W low-pressure mercury lamp for 60 minutes, and water, methanol, water, neutral detergent After washing in order of water, it was dried under reduced pressure overnight. When the obtained cloth was dyed with a differential dye (Kayastin), it showed that the surface structure of the cotton cloth was changed and the cotton cloth was modified due to the remarkable blue-purple color compared to the untreated cotton cloth. . The blue-violet color was more noticeable on the light-irradiated surface. The degree of blue-violet color was more prominent than normal cotton cloth.
Example 5
Tencel cloth was impregnated with an aqueous solution containing 3 mol / L acrylic acid and 5% hydrogen peroxide, and the pulled-up place was irradiated with a 15 W low-pressure mercury lamp for 60 minutes, followed by water, methanol, water, neutral detergent, and water in that order. And then dried under reduced pressure overnight. When the obtained cloth was dyed with a differential dye (Kayastin), it showed a remarkable reddish purple color compared to the untreated Tencel cloth. found.
Example 6
Tencel cloth was impregnated with an aqueous solution containing 0.9 mol / L methacrylic acid and 5% hydrogen peroxide, and the pulled-up place was irradiated with a 15 W low-pressure mercury lamp for 60 minutes. Water, methanol, water, neutral detergent, water After washing in this order, it was dried under reduced pressure overnight. When the obtained cloth was dyed with a differential dye (Kayastin), it showed a remarkable blue-purple color compared to the untreated Tencel cloth. found. The blue-violet color was more noticeable on the light-irradiated surface.
Example 7
Tencel cloth was impregnated with an aqueous solution containing 0.3 mol / L maleic acid and 5% hydrogen peroxide, and the pulled-up place was irradiated with a low-pressure mercury lamp of 15 W for 60 minutes, water, methanol, water, neutral detergent, water After washing in this order, it was dried under reduced pressure overnight. When the obtained cloth was dyed with a differential dye (Kayastin), the surface structure of the tencel was changed due to a slightly greenish color compared to the untreated tencel cloth, and the tencel cloth was modified. It has been found.
Example 8
A polynosic cloth is impregnated with an aqueous solution containing 3 mol / L acrylic acid and 5% hydrogen peroxide. The pulled-up place is irradiated with a 15 W low-pressure mercury lamp for 60 minutes, followed by water, methanol, water, neutral detergent, and water in that order. And then dried under reduced pressure overnight. When the obtained fabric was dyed with a differential dye (Kayastin), it showed a remarkable reddish purple color compared to the untreated polynosic fabric, indicating that the surface structure of the polynosic was changed and the polynosic fabric was modified. found. Reddish purple was more remarkable on the light-irradiated surface.
Example 9
A polynosic cloth is impregnated with an aqueous solution containing 0.9 mol / L methacrylic acid and 5% hydrogen peroxide, and the pulled-up place is irradiated with a 15 W low-pressure mercury lamp for 60 minutes. Water, methanol, water, neutral detergent, water After washing in this order, it was dried under reduced pressure overnight. When the obtained cloth was dyed with a differential dye (Kayastin), it showed a remarkable blue-purple color compared to the untreated polynosic cloth, indicating that the polynosic cloth was modified and the polynosic cloth was modified. found. The blue-violet color was more noticeable on the light-irradiated surface.
Example 10
A polynosic cloth is impregnated with an aqueous solution containing 0.3 mol / L maleic acid and 5% hydrogen peroxide, and the pulled-up place is irradiated with a 15 W low-pressure mercury lamp for 60 minutes. Water, methanol, water, neutral detergent, water After washing in this order, it was dried under reduced pressure overnight. When the obtained cloth was dyed with a differential dye (Kayastin), the surface structure of the polynosic changed due to a slightly greenish blue compared to the untreated polynosic cloth, and the polynosic cloth was modified. It has been found.
Example 11
A cupra cloth is impregnated with an aqueous solution containing 3 mol / L acrylic acid and 5% hydrogen peroxide, and a 15 W low-pressure mercury lamp is irradiated for 60 minutes to the pulled-up place, followed by water, methanol, water, neutral detergent, and water in that order. And then dried under reduced pressure overnight. When the obtained cloth was dyed with a differential dye (Kayastin), it showed a remarkable red-purple color compared to the untreated cupra cloth, which indicated that the surface structure of the cupra was changed and the cupra cloth was modified. found.
Example 12
A cupra cloth is impregnated with an aqueous solution containing 0.9 mol / L methacrylic acid and 5% hydrogen peroxide, and the pulled-up place is irradiated with a 15 W low-pressure mercury lamp for 60 minutes, and water, methanol, water, neutral detergent, water After washing in this order, it was dried under reduced pressure overnight. When the obtained cloth was dyed with a differential dye (Kayastin), it showed a remarkable blue-purple color compared to the untreated cupra cloth, indicating that the surface structure of the cupra was changed and the cupra cloth was modified. found.
Example 13
The cupra cloth was impregnated with an aqueous solution containing 0.3 mol / L maleic acid and 5% hydrogen peroxide, and the pulled-up place was irradiated with a 15 W low-pressure mercury lamp for 60 minutes, water, methanol, water, neutral detergent, water After washing in this order, it was dried under reduced pressure overnight. When the obtained cloth was dyed with a differential dye (Kayastin), it was found that the surface structure of the cupra was changed and the cupra cloth was modified due to darkening compared to the untreated cupra cloth.

本発明方法を実施するために使用される代表的な改質装置の説明図。The explanatory view of the typical reformer used in order to carry out the method of the present invention. 本発明方法を実施するために使用される他の代表的な改質装置の説明図。Explanatory drawing of the other typical reforming apparatus used in order to implement this invention method. 本発明方法を実施するために使用される更に他の代表的な改質装置の説明図。An explanatory view of still another typical reformer used for carrying out the method of the present invention. 本発明方法を実施するために使用される更に他の代表的な改質装置の説明図。An explanatory view of still another typical reformer used for carrying out the method of the present invention.

Claims (8)

光照射によりラジカルを発生する化合物と電子吸引性基が直接炭素−炭素二重結合を形成する炭素原子に結合した炭素−炭素二重結合を有する化合物の存在下、セルロース系繊維(アスペクト比が300以下で、その存在比が全体の60%以上のセルロース系繊維を除く)又は動物性繊維を含む、繊維又は繊維製品に対し、光照射することを特徴とする繊維又は繊維製品の改質方法。   Cellulose fibers (with an aspect ratio of 300) in the presence of a compound that generates radicals upon light irradiation and a compound having a carbon-carbon double bond in which an electron-withdrawing group is directly bonded to a carbon atom that forms a carbon-carbon double bond. In the following, a method for modifying a fiber or a fiber product, which comprises irradiating a fiber or a fiber product containing an animal fiber (excluding cellulosic fibers having an abundance ratio of 60% or more) or an animal fiber. 光照射によりラジカルを発生する化合物の存在下、セルロース系繊維(アスペクト比が300以下で、その存在比が全体の60%以上のセルロース系繊維を除く)又は動物性繊維を含む、繊維又は繊維製品に対し、光照射した後に、前記該炭素−炭素二重結合を有する化合物と処理することを特徴とする繊維又は繊維製品の改質方法。   Fibers or fiber products containing cellulosic fibers (excluding cellulosic fibers having an aspect ratio of 300 or less and an abundance ratio of 60% or more) or animal fibers in the presence of a compound that generates radicals upon irradiation with light. On the other hand, after the light irradiation, it is treated with the compound having the carbon-carbon double bond. 光照射によりラジカルを発生する化合物を、セルロース系繊維又は動物性繊維を含む、繊維又は繊維製品の一部だけに付与して光照射することを特徴とする請求項1又は2に記載の繊維又は繊維製品の改質方法。   The fiber according to claim 1 or 2, wherein a compound that generates radicals upon light irradiation is applied to only a part of a fiber or a fiber product including cellulosic fibers or animal fibers, and is irradiated with light. A method for modifying textile products. 光照射によりラジカルを発生する化合物が過酸化物であることを特徴とする請求項1から3のいずれかに記載の繊維又は繊維製品の改質方法。   The method for modifying a fiber or fiber product according to any one of claims 1 to 3, wherein the compound that generates radicals upon irradiation with light is a peroxide. 光ビームまたはマスクを通して光照射を行うことを特徴とする請求項1から4のいずれかに記載の繊維又は繊維製品の改質方法。   5. The method for modifying a fiber or fiber product according to claim 1, wherein light irradiation is performed through a light beam or a mask. 請求項1から5のいずれかに記載の方法での光照射後に繊維及び繊維製品を還元剤で処理することを特徴とする繊維及び繊維製品の改質方法。   A method for modifying a fiber and a fiber product, wherein the fiber and the fiber product are treated with a reducing agent after the light irradiation by the method according to any one of claims 1 to 5. 請求項1、3から6のいずれかに記載の方法を行うための改質装置であって、光源とともに光照射によりラジカルを発生する化合物と前記炭素−炭素二重結合を有する化合物の存在下でセルロース系繊維又は動物性繊維を含む、繊維又は繊維製品に光照射する手段を備えていることを特徴とする繊維又は繊維製品の改質装置。   A reformer for carrying out the method according to any one of claims 1, 3 to 6, in the presence of a compound that generates a radical by light irradiation together with a light source and a compound having the carbon-carbon double bond. An apparatus for modifying a fiber or a fiber product, comprising means for irradiating light to the fiber or the fiber product including cellulosic fibers or animal fibers. 請求項2から6のいずれかに記載の方法を行うための改質装置であって、光源とともに、光照射によりラジカルを発生する化合物の存在下でセルロース系繊維又は動物性繊維を含む、繊維又は繊維製品に光照射する手段と、光照射した後に該炭素−炭素二重結合を有する化合物と処理する手段を備えていることを特徴とする繊維又は繊維製品の改質装置。   A reformer for carrying out the method according to any one of claims 2 to 6, comprising a fiber or a cellulosic fiber or animal fiber in the presence of a light source and a compound that generates radicals by light irradiation. An apparatus for modifying a fiber or a textile product, comprising: means for irradiating a fiber product with light; and means for treating with a compound having a carbon-carbon double bond after the light irradiation.
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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2014524522A (en) * 2011-08-17 2014-09-22 スリーエム イノベイティブ プロパティズ カンパニー Monomer grafted fiber and use thereof
US10697111B2 (en) 2008-04-30 2020-06-30 Xyleco, Inc. Textiles and methods and systems for producing textiles
KR20210007173A (en) * 2019-07-10 2021-01-20 주식회사 원텍스 Complex Fabrics Comprising Washable Wool Woven Fabrics

Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57500546A (en) * 1980-05-12 1982-04-01
JPS6233876A (en) * 1985-07-31 1987-02-13 東レ株式会社 Production of composite sheet
JPS63260906A (en) * 1987-04-17 1988-10-27 Mitsubishi Petrochem Co Ltd Manufacture of water-absorptive composite material
JPH01121306A (en) * 1987-11-06 1989-05-15 Mitsubishi Petrochem Co Ltd Production of water absorbing complex
JPH0284524A (en) * 1988-07-20 1990-03-26 Kanebo Ltd Moisture absorption processing of woven and knitted fabric of wool
JPH04202865A (en) * 1990-11-29 1992-07-23 Toray Ind Inc Production of colored yarn structure
JPH08109228A (en) * 1993-09-18 1996-04-30 Hitoshi Kanazawa Method of surface-modifying polymeric material
JP2002201297A (en) * 2000-11-02 2002-07-19 Hitoshi Kanazawa Method for modifying polymeric material, and its application
JP2002332321A (en) * 2001-05-08 2002-11-22 Japan Atom Energy Res Inst Method for subjecting fibrous substance to radiation graft polymerization treatment and its apparatus
JP2009068139A (en) * 2007-09-13 2009-04-02 National Institute Of Advanced Industrial & Technology Method for modifying synthetic fiber or fiber product and apparatus therefor

Patent Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57500546A (en) * 1980-05-12 1982-04-01
JPS6233876A (en) * 1985-07-31 1987-02-13 東レ株式会社 Production of composite sheet
JPS63260906A (en) * 1987-04-17 1988-10-27 Mitsubishi Petrochem Co Ltd Manufacture of water-absorptive composite material
JPH01121306A (en) * 1987-11-06 1989-05-15 Mitsubishi Petrochem Co Ltd Production of water absorbing complex
JPH0284524A (en) * 1988-07-20 1990-03-26 Kanebo Ltd Moisture absorption processing of woven and knitted fabric of wool
JPH04202865A (en) * 1990-11-29 1992-07-23 Toray Ind Inc Production of colored yarn structure
JPH08109228A (en) * 1993-09-18 1996-04-30 Hitoshi Kanazawa Method of surface-modifying polymeric material
JP2002201297A (en) * 2000-11-02 2002-07-19 Hitoshi Kanazawa Method for modifying polymeric material, and its application
JP2002332321A (en) * 2001-05-08 2002-11-22 Japan Atom Energy Res Inst Method for subjecting fibrous substance to radiation graft polymerization treatment and its apparatus
JP2009068139A (en) * 2007-09-13 2009-04-02 National Institute Of Advanced Industrial & Technology Method for modifying synthetic fiber or fiber product and apparatus therefor

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10697111B2 (en) 2008-04-30 2020-06-30 Xyleco, Inc. Textiles and methods and systems for producing textiles
JP2014524522A (en) * 2011-08-17 2014-09-22 スリーエム イノベイティブ プロパティズ カンパニー Monomer grafted fiber and use thereof
KR20210007173A (en) * 2019-07-10 2021-01-20 주식회사 원텍스 Complex Fabrics Comprising Washable Wool Woven Fabrics
KR102411625B1 (en) 2019-07-10 2022-06-20 주식회사 원텍스 Complex Fabrics Comprising Washable Wool Woven Fabrics

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