JP2003020568A - Endothermic treating agent for fiber material - Google Patents

Endothermic treating agent for fiber material

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Publication number
JP2003020568A
JP2003020568A JP2001206470A JP2001206470A JP2003020568A JP 2003020568 A JP2003020568 A JP 2003020568A JP 2001206470 A JP2001206470 A JP 2001206470A JP 2001206470 A JP2001206470 A JP 2001206470A JP 2003020568 A JP2003020568 A JP 2003020568A
Authority
JP
Japan
Prior art keywords
meth
resin
endothermic
acrylic acid
fiber material
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.)
Pending
Application number
JP2001206470A
Other languages
Japanese (ja)
Inventor
Masahiro Tanno
正宏 丹野
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.)
Kyoeisha Chemical Co Ltd
Original Assignee
Kyoeisha Chemical Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Kyoeisha Chemical Co Ltd filed Critical Kyoeisha Chemical Co Ltd
Priority to JP2001206470A priority Critical patent/JP2003020568A/en
Publication of JP2003020568A publication Critical patent/JP2003020568A/en
Pending legal-status Critical Current

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Abstract

PROBLEM TO BE SOLVED: To provide an endothermic treating agent for fiber materials having excellent washing resistance and useful for imparting endothermic property to a fiber material for the manufacture of garments. SOLUTION: The endothermic treating agent for fiber materials contains a resin produced by the crosslinking polymerization of xylitol through crosslinking groups. The endothermic resin is a polymer of an ester of xylitol and (meth)acrylic acid or a copolymer of an ester of xylitol and (meth)acrylic acid and an ester selected from an ester of a monool and (meth)acrylic acid and an ester of a diol and (meth)acrylic acid.

Description

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

【0001】[0001]

【発明の属する技術分野】本発明は、着衣したとき清涼
感のある衣服とするため、衣服用の繊維素材に吸熱性を
付与する加工処理を施す際に使用される繊維素材用吸熱
加工剤に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a heat absorbing agent for a fiber material, which is used for giving a heat absorbing property to a fiber material for a garment in order to obtain a garment having a refreshing feeling when it is dressed. It is a thing.

【0002】[0002]

【従来の技術】衣服には、例えば、綿のようなセルロー
ス繊維製のものや、アクリル繊維のような合成繊維製の
ものがある。
2. Description of the Related Art Clothing includes, for example, those made of cellulose fibers such as cotton and those made of synthetic fibers such as acrylic fibers.

【0003】綿製の衣服は、水分の吸収性が優れている
反面、乾燥速度が遅く、着衣時の発汗や外気の湿気で湿
ってしまうと乾き難いうえ、このような水分を吸収した
ときの水和熱による発熱のために、不快に感じることが
ある。快適に綿性の衣服を着衣できるように、例えば、
この衣服の繊維素材である生地に、予め疎水性の樹脂を
塗布して含水率を低下させる加工方法が知られている。
While cotton clothes are excellent in absorbing water, they dry slowly and are difficult to dry if they become sweaty when they are dressed or if they are wet by the humidity of the outside air. May feel uncomfortable due to the heat of hydration. To be able to wear cotton clothes comfortably, for example,
There is known a processing method in which a hydrophobic resin is previously applied to a cloth which is a fiber material of the garment to reduce the water content.

【0004】また、合成繊維製の衣服は、水分の吸収性
が悪いので、汗等を吸収せず蒸れてしまい、不快に感じ
ることがある。そこで、合成繊維製の生地に吸水性を付
与するグリセリン誘導体、糖エステル誘導体、ポリエチ
レングリコール誘導体、または多糖類をバインダーとと
もに塗布する加工方法が知られている。
Further, since clothes made of synthetic fiber have poor absorbency of water, they may feel uncomfortable because they do not absorb sweat or the like and become damp. Therefore, a processing method is known in which a glycerin derivative, a sugar ester derivative, a polyethylene glycol derivative or a polysaccharide which imparts water absorbability to a synthetic fiber cloth is applied together with a binder.

【0005】しかし、これらの加工方法では、衣服の十
分な快適性と耐洗濯性とが得られず、経済的にも満足で
きるものではない。
However, with these processing methods, sufficient comfort and washing resistance of clothes cannot be obtained, which is not economically satisfactory.

【0006】[0006]

【発明が解決しようとする課題】本発明は、衣服へと縫
製される繊維素材に、清涼性を付与する加工処理を施す
際に使用される、耐洗濯性の優れた繊維素材用吸熱加工
剤を提供することを目的とする。
DISCLOSURE OF THE INVENTION The present invention provides an endothermic processing agent for a textile material having excellent washing resistance, which is used when a textile material sewn into clothes is subjected to a processing treatment for imparting a cooling property. The purpose is to provide.

【0007】[0007]

【課題を解決するための手段】前記の目的を達成するた
めになされた本発明の繊維素材用吸熱加工剤は、キシリ
トールが架橋基を介して架橋重合した樹脂を含有してな
るものである。この樹脂が、キシリトール由来の基を含
有しているため、吸熱性を発現する。
The endothermic processing agent for fiber materials of the present invention made to achieve the above object comprises a resin in which xylitol is cross-linked and polymerized through a cross-linking group. Since this resin contains a group derived from xylitol, it exhibits an endothermic property.

【0008】この樹脂が、キシリトールと(メタ)アクリ
ル酸とのエステルの重合物であることが好ましい。架橋
基が(メタ)アクリル酸のような不飽和基であると、熱や
光で速やかに重合する結果、キシリトールが架橋基を介
して架橋する。
This resin is preferably a polymer of an ester of xylitol and (meth) acrylic acid. When the cross-linking group is an unsaturated group such as (meth) acrylic acid, xylitol is cross-linked through the cross-linking group as a result of rapid polymerization by heat or light.

【0009】この樹脂は、キシリトールと(メタ)アクリ
ル酸とのエステルを、モノオールと(メタ)アクリル酸と
のエステル、およびジオールと(メタ)アクリル酸とのジ
エステルのいずれかのエステルと共重合させた重合物で
あってもよい。共重合した重合物中のキシリトールと
(メタ)アクリル酸とのエステルの構成比率が、少なくと
も30重量%であることが好ましい。50重量%以上で
あるとより一層好ましい。
This resin is obtained by copolymerizing an ester of xylitol and (meth) acrylic acid with an ester of monool and (meth) acrylic acid or a diester of diol and (meth) acrylic acid. It may be a polymerized product. With xylitol in the copolymerized polymer
The composition ratio of the ester with (meth) acrylic acid is preferably at least 30% by weight. It is even more preferably 50% by weight or more.

【0010】モノオールと(メタ)アクリル酸とのエステ
ルは、2−ヒドロキシエチル(メタ)アクリレート、2−
ヒドロキシプロピル(メタ)アクリレート、ポリエチレン
グリコールモノメタクリレート、メトキシポリエチレン
グリコール(メタ)アクリレート、グリシジル(メタ)アク
リレート、および2−ヒドロキシブチル(メタ)アクリレ
ートのいずれかであることが好ましい。ポリエチレング
リコールモノメタクリレートは、数平均分子量90〜3
50のポリエチレングリコールを用いて調製されたもの
であると一層好ましい。
Esters of monool and (meth) acrylic acid include 2-hydroxyethyl (meth) acrylate and 2-hydroxyethyl (meth) acrylate.
It is preferably any one of hydroxypropyl (meth) acrylate, polyethylene glycol monomethacrylate, methoxypolyethylene glycol (meth) acrylate, glycidyl (meth) acrylate, and 2-hydroxybutyl (meth) acrylate. Polyethylene glycol monomethacrylate has a number average molecular weight of 90 to 3
More preferably, it was prepared using 50 polyethylene glycol.

【0011】ジオールと(メタ)アクリル酸とのジエステ
ルは、ポリエチレングリコール−300 ジ(メタ)アク
リレートやポリエチレングリコール−400 ジ(メタ)
アクリレートのようなポリエチレングリコールジ(メタ)
アクリレート、およびグリセロールジメタクリレートの
いずれかであることが好ましい。
Diesters of diol and (meth) acrylic acid include polyethylene glycol-300 di (meth) acrylate and polyethylene glycol-400 di (meth) acrylate.
Polyethylene glycol di (meth) such as acrylate
It is preferably either acrylate or glycerol dimethacrylate.

【0012】繊維素材用吸熱加工剤には、グリオキザー
ル樹脂およびメラミン樹脂のいずれかの熱架橋性樹脂が
含まれていてもよい。グリオキザール樹脂には例えばス
ミテックスレジンNS−200(住友化学(株)製の商品
名)が挙げられ、メラミン樹脂には例えばスミテックス
レジンM−3(住友化学(株)製の商品名)が挙げられ
る。
The endothermic processing agent for fiber materials may contain a thermally crosslinkable resin of either glyoxal resin or melamine resin. The Glyoxal resin includes, for example, Sumitex Resin NS-200 (trade name of Sumitomo Chemical Co., Ltd.), and the melamine resin includes, for example, Sumitex Resin M-3 (trade name of Sumitomo Chemical Co., Ltd.). To be

【0013】本発明の繊維素材処理方法は、前記の繊維
素材用吸熱加工剤を含んでいる水溶液に、繊維素材を浸
漬し、脱水、乾燥後、加熱するというものである。
The textile material treating method of the present invention comprises immersing the textile material in an aqueous solution containing the above-mentioned endothermic processing agent for textile materials, dehydrating and drying, and then heating.

【0014】加熱は、110〜170℃であることが好
ましい。
The heating is preferably 110 to 170 ° C.

【0015】繊維素材は、綿や麻のようなセルロース繊
維、レーヨンやアセテート人絹のような再生繊維、ナイ
ロンやポリエステル系合成繊維やアクリル系合成繊維の
ような合成繊維、およびその混紡繊維であってもよく、
またこれらの編物、織物、不織布であってもよい。中で
も天竺すなわち綿製織物などのニット生地であると一層
好ましい。
The fiber materials are cellulose fibers such as cotton and hemp, recycled fibers such as rayon and acetate human silk, synthetic fibers such as nylon and polyester synthetic fibers and acrylic synthetic fibers, and blended fibers thereof. Maybe,
Moreover, these knitted fabrics, woven fabrics, and non-woven fabrics may be used. Above all, it is more preferable to use a knit fabric such as a plain cloth, that is, a cotton fabric.

【0016】繊維素材用吸熱加工剤のキシリトール含有
樹脂や熱架橋性樹脂が、浸漬によって繊維素材の繊維の
隙間に浸入し、乾燥後の加熱によって架橋し高分子量化
して、繊維素材の表面に被覆して固着する。この繊維素
材を縫製した衣服を着衣しているときに衣服が水分を吸
収しても、キシリトール基が存在するために、その吸熱
作用によって、清涼であると感ずる。綿製の衣服のよう
に水分の吸入によって水和熱が発生した場合でも、吸熱
作用によって、水和熱の発熱を緩和する。
A xylitol-containing resin or a heat-crosslinkable resin, which is an endothermic finishing agent for a fiber material, penetrates into the interstices between the fibers of the fiber material by immersion, and is crosslinked to have a high molecular weight by heating after drying to coat the surface of the fiber material. And stick. Even if the garment absorbs water when the garment sewn with this fiber material is put on, it feels that it is refreshing due to its endothermic action because of the presence of the xylitol group. Even when heat of hydration is generated by inhalation of water such as cotton clothes, the endothermic action alleviates the heat of hydration.

【0017】そのため、この処理の施された繊維素材か
ら作られた衣服は、着衣時の汗や湿気のような水分を吸
収しても、不快感がなく、清涼感がある。さらに優れた
柔軟性を有しているので、着心地がよい。衣服を繰り返
して洗濯しても、清涼感や柔軟性が損なわれない。
Therefore, the garment made of the fiber material subjected to this treatment has no discomfort and a refreshing feeling even if it absorbs moisture such as sweat and moisture when it is put on. Further, it has excellent flexibility and is comfortable to wear. Repeated washing of clothes does not impair the refreshing feeling and flexibility.

【0018】[0018]

【実施例】本発明を適用する繊維素材用吸熱加工剤の実
施例について詳細に説明する。
[Examples] Examples of endothermic processing agents for fiber materials to which the present invention is applied will be described in detail.

【0019】以下の実施例1および2は、本発明を適用
する繊維素材用吸熱加工剤の調製例を示し、比較例1〜
5は本発明を適用外の繊維素材用加工剤の調製例を示
す。
Examples 1 and 2 below show preparation examples of endothermic processing agents for fiber materials to which the present invention is applied, and Comparative Examples 1 to 1
Reference numeral 5 shows an example of preparation of a processing agent for fiber materials to which the present invention is not applied.

【0020】(実施例1)キシリトールメタクリレート
100重量部、2−ヒドロキシエチルメタクリレート5
0重量部、およびイオン交換水850重量部を混合し、
その全量に対し0.5重量%のアゾ系重合開始剤を加え
た。この混合液に窒素を吹き込みながら60℃に昇温
し、同温で5時間反応させたところ、キシリトールメタ
クリレートと2−ヒドロキシエチルメタクリレートとが
共重合し、粘度10mpa・sの樹脂含有水溶液を得
た。
Example 1 100 parts by weight of xylitol methacrylate, 5-hydroxyethyl methacrylate 5
0 parts by weight and 850 parts by weight of deionized water are mixed,
0.5% by weight of the total amount of the azo-based polymerization initiator was added. The temperature was raised to 60 ° C. while blowing nitrogen into this mixed liquid, and the reaction was carried out at the same temperature for 5 hours. As a result, xylitol methacrylate and 2-hydroxyethyl methacrylate were copolymerized to obtain a resin-containing aqueous solution having a viscosity of 10 mpa · s. .

【0021】この樹脂水溶液20重量部に、グリオキザ
ール樹脂であるスミテックスレジンNS−200(住友
化学(株)製の商品名)3重量部、高分子量化触媒である
スミテックスレジンMX(住友化学(株)製の商品名)
0.5重量部、水76.5重量部を加えて混合し、繊維
素材用吸熱加工剤を得た。
To 20 parts by weight of this resin aqueous solution, 3 parts by weight of Sumitex Resin NS-200 (trade name of Sumitomo Chemical Co., Ltd.) which is a glyoxal resin, and Sumitex Resin MX (Sumitomo Chemical ( (Trade name)
0.5 parts by weight and 76.5 parts by weight of water were added and mixed to obtain an endothermic processing agent for fiber materials.

【0022】(実施例2)実施例1で調製して得た樹脂
含有水溶液20重量部に、メラミン樹脂であるスミテッ
クスレジンM−3(住友化学(株)製の商品名)0.3重
量部、触媒であるスミテックスアクセレレーターX−1
10(住友化学(株)製の商品名)0.1重量部、水7
9.6重量部を加えて混合し、繊維素材用吸熱加工剤を
得た。
(Example 2) 0.3 parts by weight of Sumitex Resin M-3 (trade name of Sumitomo Chemical Co., Ltd.), which is a melamine resin, was added to 20 parts by weight of the resin-containing aqueous solution prepared in Example 1. Part, catalyst Sumitex Accelerator X-1
10 (trade name of Sumitomo Chemical Co., Ltd.) 0.1 part by weight, water 7
9.6 parts by weight were added and mixed to obtain an endothermic processing agent for fiber materials.

【0023】(比較例1)グルコシルオキシエチルメタ
アクリレート70重量部、2−ヒドロキシエチルメタク
リレート30重量部、これらアクリレートの合計量に対
し0.1重量%のスミテックスアクセレレーターX−1
10、およびイオン交換水900重量部を混合した。こ
の混合液に窒素を吹き込みながら60℃に昇温し、同温
で6時間反応させたところ、グルコシルオキシエチルメ
タアクリレートと2−ヒドロキシエチルメタクリレート
とが共重合し、粘度12mpa・sの樹脂含有水溶液を
得た。その後は実施例1と同様にして、繊維素材用吸熱
剤を得た。
Comparative Example 1 70 parts by weight of glucosyloxyethyl methacrylate, 30 parts by weight of 2-hydroxyethyl methacrylate, and 0.1% by weight of the total amount of these acrylates, Sumitex Accelerator X-1.
10 and 900 parts by weight of ion-exchanged water were mixed. The temperature was raised to 60 ° C. while blowing nitrogen into this mixed solution, and the reaction was carried out at the same temperature for 6 hours. As a result, glucosyloxyethyl methacrylate and 2-hydroxyethyl methacrylate were copolymerized, and a resin-containing aqueous solution having a viscosity of 12 mpa · s was obtained. Got Thereafter, in the same manner as in Example 1, a heat absorbing agent for fiber material was obtained.

【0024】(比較例2)D−マンノシルエチルメタク
リレート100重量部、2−ヒドロキシエチルメタクリ
レート50重量部、これらアクリレートの合計量に対し
0.1重量%のアゾ系重合開始剤、およびイオン交換水
850重量部を混合した。この混合液に窒素を吹き込み
ながら50℃に昇温し、同温で5時間反応させたとこ
ろ、D−マンノシルエチルメタクリレートと2−ヒドロ
キシエチルメタクリレートとが共重合し、粘度15mp
a・sの樹脂含有水溶液を得た。その後は実施例1と同
様にして、繊維素材用加工剤を得た。
Comparative Example 2 100 parts by weight of D-mannosylethyl methacrylate, 50 parts by weight of 2-hydroxyethyl methacrylate, 0.1% by weight of an azo-based polymerization initiator with respect to the total amount of these acrylates, and ion-exchanged water 850. Parts by weight were mixed. The temperature was raised to 50 ° C. while blowing nitrogen into this mixed solution, and the reaction was carried out at the same temperature for 5 hours. As a result, D-mannosylethyl methacrylate and 2-hydroxyethyl methacrylate were copolymerized, and the viscosity was 15 mp.
A resin-containing aqueous solution of a · s was obtained. Thereafter, in the same manner as in Example 1, a textile material processing agent was obtained.

【0025】(比較例3)糖アルコールであるキシリト
ール3重量部、熱架橋性樹脂であるスミテックスレジン
M−3の0.3重量部、触媒であるスミテックスアクセ
レレーターX−110の0.1重量部、水96.6重量
部を混合して繊維素材用加工剤を得た。
(Comparative Example 3) 3 parts by weight of xylitol which is a sugar alcohol, 0.3 part by weight of Sumitex resin M-3 which is a thermally crosslinkable resin, and 0. 0 parts of a catalyst of Sumitex Accelerator X-110. 1 part by weight and 96.6 parts by weight of water were mixed to obtain a processing agent for fiber materials.

【0026】(比較例4)糖アルコールであるキシリト
ール5重量部、ノニオン性のシリコーン・アクリルコポ
リマーの水溶性アクリルバインダーであるライトエポッ
クS−60NFE(共栄社化学(株)製の商品名)5重量
部、ノニオン性の水溶性ウレタンポリマーであるライト
レジンUN−11(共栄社化学(株)社製の商品名)5重
量部、水85重量部を混合して繊維素材用加工剤を得
た。
Comparative Example 4 5 parts by weight of xylitol which is a sugar alcohol, and 5 parts by weight of Light Epoch S-60NFE (a trade name of Kyoeisha Chemical Co., Ltd.) which is a water-soluble acrylic binder of a nonionic silicone-acrylic copolymer. , 5 parts by weight of light resin UN-11 (trade name of Kyoeisha Chemical Co., Ltd.), which is a nonionic water-soluble urethane polymer, and 85 parts by weight of water were mixed to obtain a textile material processing agent.

【0027】(比較例5)五単糖キシロース5重量部、
熱架橋性樹脂であるスミテックスレジンNS−200の
5重量部、触媒であるスミテックスアクセレレーターX
−110の2重量部、水88重量部を混合して繊維素材
用加工剤を得た。
(Comparative Example 5) 5 parts by weight of pentose sugar xylose,
5 parts by weight of Sumitex Resin NS-200, which is a heat-crosslinkable resin, and Sumitex Accelerator X, which is a catalyst.
2 parts by weight of -110 and 88 parts by weight of water were mixed to obtain a textile material processing agent.

【0028】実施例1〜2で得られた繊維素材用吸熱加
工剤および比較例1〜5で得られた加工剤を用いて処理
した繊維素材の耐洗濯性試験を行い、洗濯前後の繊維素
材の吸熱性と、柔軟性との各性能について以下のように
評価した。
A washing resistance test was conducted on the fiber materials treated with the endothermic processing agents for fiber materials obtained in Examples 1-2 and the processing agents obtained in Comparative Examples 1-5, and the fiber materials before and after washing were tested. The endothermic properties and the respective performances of flexibility were evaluated as follows.

【0029】先ず、繊維素材として用いる試験布を作製
した。35%過酸化水素水3g、苛性ソーダ1g、メタ
ケイ酸ソーダ0.5g、ノニオン界面活性剤とアニオン
界面活性剤とを主成分として含有する精練剤ライトステ
ップSKY(共栄社化学(株)製の商品名)1g、浴中柔
軟剤用高分子化合物を主成分として含有する繊維保護剤
であるスレノンP−4871(共栄社化学(株)製の商品
名)1gを、水に溶解し、1Lとした精練漂白用水溶液
を調製した。30cm四方の生成り綿ニット天竺を精練
するため、この溶液を精練漂白浴に入れた。天竺とこの
水溶液との体積比すなわち浴比が1:20となるよう
に、天竺を漬け、95℃で30分間精練した。その後、
天竺を水洗し、絞ってから、110℃で乾燥した。
First, a test cloth used as a fiber material was prepared. 3% of 35% hydrogen peroxide water, 1 g of caustic soda, 0.5 g of sodium metasilicate, a scouring agent LightStep SKY (trade name of Kyoeisha Chemical Co., Ltd.) containing a nonionic surfactant and an anionic surfactant as main components. 1 g, 1 g of Srenone P-4871 (trade name of Kyoeisha Chemical Co., Ltd.), which is a fiber protective agent containing a polymer compound for bath softener as a main component, was dissolved in water to 1 L for scouring and bleaching. An aqueous solution was prepared. This solution was placed in a scouring bleaching bath in order to scouring a 30 cm square produced cotton knit cloth. The cloth was soaked so that the volume ratio between the cloth and the aqueous solution, that is, the bath ratio was 1:20, and scouring was carried out at 95 ° C. for 30 minutes. afterwards,
The cloth was washed with water, squeezed and dried at 110 ° C.

【0030】実施例1〜4および比較例1〜3の各々の
繊維素材用吸熱加工剤に、この天竺を浸漬後、マングル
により、80〜120%に絞った。その後、恒温槽に入
れて110℃で4分間乾燥した。次いで150℃で2分
間加熱すると、樹脂がさらに架橋して高分子量化した重
合体が天竺上に形成された試験布が得られた。
After dipping the cloth in each of the endothermic processing agents for fiber materials of Examples 1 to 4 and Comparative Examples 1 to 3, it was squeezed to 80 to 120% by a mangle. Then, it put into a thermostat and dried at 110 degreeC for 4 minutes. Then, it was heated at 150 ° C. for 2 minutes to obtain a test cloth in which a polymer having a higher molecular weight by further crosslinking the resin was formed on the cloth.

【0031】夫々の試験布を2群に分け、うち1群は洗
濯せず、他の1群は洗濯し、洗濯前後の吸熱性の低下の
有無により、耐洗濯性について調べた。
Each test cloth was divided into two groups, one group was not washed, the other group was washed, and the resistance to washing was examined by the presence or absence of a decrease in heat absorption before and after washing.

【0032】洗濯には、合成洗剤を上水道水に溶解した
2g/Lの濃度の洗剤水溶液を使用した。試験布とこの
洗剤水溶液との浴比を1:50として、5分間ずつ10
回洗濯を繰り返した後、上水道水で2分間ずつ5回濯ぎ
を繰り返し、絞って脱水してから、110℃で乾燥し
た。
For washing, an aqueous detergent solution having a concentration of 2 g / L in which a synthetic detergent was dissolved in tap water was used. The test cloth and the aqueous solution of this detergent were set to a bath ratio of 1:50, and the bath ratio was 10 for 5 minutes each.
After repeating washing twice, rinsing was repeated 5 times for 2 minutes each with tap water, squeezed to dehydrate, and then dried at 110 ° C.

【0033】洗濯していない試験布と洗濯した試験布と
を、順次半分に3回折って8層に折り重ね、熱風循環式
乾燥機を用い、120℃で30分乾燥した後、デシケー
タ中で24時間放冷した。この折り重ねた試験布に温度
センサーを挟み、30℃、相対湿度90%RHの恒温恒
湿槽に入れた。このときの試験布の温度と、ブランクと
して未処理試験布とを比較した。ブランクに比べた試験
布の温度が2℃以上低くて優れた吸熱性を示していた試
験布を◎、2℃未満低い吸熱性を示していた試験布を
○、吸熱性を示さなかった試験布を×とする3段階で評
価した。
The unwashed test cloth and the washed test cloth were sequentially folded in half into three folds and folded into eight layers, dried at 120 ° C. for 30 minutes using a hot air circulation dryer, and then placed in a desiccator. It was left to cool for 24 hours. A temperature sensor was sandwiched between the folded test cloths, and the test cloths were placed in a thermo-hygrostat at 30 ° C. and a relative humidity of 90% RH. The temperature of the test cloth at this time was compared with the untreated test cloth as a blank. The test cloth having a temperature lower than that of the blank by 2 ° C. or more showed excellent heat absorption, ◎, the test cloth having a heat absorption lower than 2 ° C., the test cloth having no heat absorption. Was evaluated in three stages with x as x.

【0034】また、洗濯後の試験布の柔軟性について、
目視による観察および手で擦った時の触感について調べ
た。
Regarding the flexibility of the test cloth after washing,
The visual observation and the tactile sensation when rubbed with hands were examined.

【0035】その結果を、表1に示す。The results are shown in Table 1.

【0036】[0036]

【表1】 [Table 1]

【0037】表1に示すとおり、実施例1および2のよ
うにキシリトールメタクリレートと2−ヒドロキシメタ
ルメタクリレートとの共重合物を含む繊維素材用吸熱加
工剤を用いて処理を施した布は、吸熱性と柔軟性とに優
れている。一方、比較例1〜5のようにキシリトールを
含まない加工剤、またはキシリトールを単体で含む加工
剤は、吸熱性が悪く、柔軟性がない。
As shown in Table 1, the cloths treated with the endothermic processing agent for fiber materials containing the copolymer of xylitol methacrylate and 2-hydroxymetal methacrylate as in Examples 1 and 2 had endothermic properties. And excellent in flexibility. On the other hand, the processing agent containing no xylitol or the processing agent containing xylitol alone as in Comparative Examples 1 to 5 has poor endotherm and lacks flexibility.

【0038】[0038]

【発明の効果】以上、詳細に説明したように、本発明の
繊維素材用吸熱加工剤を用いて処理した生地から縫製さ
れた衣服等は、水分を吸収したときに吸熱性を発現する
ものであり、そのため汗等で濡れても清涼感がある。ま
たこのような衣服は、耐洗濯性を有し、繰り返し洗濯し
ても清涼感を損なうことがなく、さらに柔軟性であるた
め着心地がよい。
As described above in detail, clothes and the like sewn from the cloth treated with the heat absorbing agent for textile material of the present invention exhibit heat absorbing property when absorbing water. There is a refreshing feeling even if it gets wet with sweat. In addition, such clothes have wash resistance, do not impair the refreshing feeling even after repeated washing, and are soft and comfortable to wear.

Claims (6)

【特許請求の範囲】[Claims] 【請求項1】 キシリトールが架橋基を介して架橋重
合した樹脂を含有してなることを特徴とする繊維素材用
吸熱加工剤。
1. An endothermic processing agent for a fiber material, which comprises a resin in which xylitol is cross-linked and polymerized through a cross-linking group.
【請求項2】 前記樹脂が、キシリトールと(メタ)ア
クリル酸とのエステルの重合物であることを特徴とする
請求項1に記載の繊維素材用吸熱加工剤。
2. The endothermic processing agent for a fiber material according to claim 1, wherein the resin is a polymer of an ester of xylitol and (meth) acrylic acid.
【請求項3】 前記樹脂が、キシリトールと(メタ)ア
クリル酸とのエステルを、モノオールと(メタ)アクリル
酸とのエステル、およびジオールと(メタ)アクリル酸と
のジエステルのいずれかのエステルと共重合させた樹脂
であることを特徴とする請求項1に記載の繊維素材用吸
熱加工剤。
3. The resin comprises an ester of xylitol and (meth) acrylic acid, an ester of monool and (meth) acrylic acid, and an ester of diol and diester of (meth) acrylic acid. The endothermic processing agent for fiber material according to claim 1, which is a copolymerized resin.
【請求項4】 前記モノオールと(メタ)アクリル酸と
のエステルが、2−ヒドロキシエチル(メタ)アクリレー
ト、2−ヒドロキシプロピル(メタ)アクリレート、ポリ
エチレングリコールモノメタクリレート、メトキシポリ
エチレングリコール(メタ)アクリレート、グリシジル
(メタ)アクリレート、および2−ヒドロキシブチル(メ
タ)アクリレートのいずれかであり、ジオールと(メタ)
アクリル酸とのジエステルが、ポリエチレングリコール
ジ(メタ)アクリレートおよびグリセロールジメタクリレ
ートのいずれかであることを特徴とする請求項3に記載
の繊維素材用吸熱加工剤。
4. The ester of monool and (meth) acrylic acid is 2-hydroxyethyl (meth) acrylate, 2-hydroxypropyl (meth) acrylate, polyethylene glycol monomethacrylate, methoxy polyethylene glycol (meth) acrylate, Glycidyl
Either (meth) acrylate or 2-hydroxybutyl (meth) acrylate, and diol and (meth)
The endothermic processing agent for fiber materials according to claim 3, wherein the diester with acrylic acid is any one of polyethylene glycol di (meth) acrylate and glycerol dimethacrylate.
【請求項5】 グリオキザール樹脂およびメラミン樹
脂のいずれかの熱架橋性樹脂が含まれていることを特徴
とする請求項1〜3のいずれかに記載の繊維素材用吸熱
加工剤。
5. The endothermic processing agent for a fiber material according to claim 1, which contains a thermally crosslinkable resin of either a glyoxal resin or a melamine resin.
【請求項6】 請求項1〜3のいずれかに記載の繊維
素材用吸熱加工剤を含んでいる水溶液に、繊維素材を浸
漬し、脱水、乾燥後、加熱することを特徴とする繊維素
材処理方法。
6. A fiber material treatment, which comprises immersing the fiber material in an aqueous solution containing the endothermic processing agent for fiber material according to any one of claims 1 to 3, dehydrating, drying, and then heating. Method.
JP2001206470A 2001-07-06 2001-07-06 Endothermic treating agent for fiber material Pending JP2003020568A (en)

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