JP2009161898A - Glove insert made of plant-originated component - Google Patents

Glove insert made of plant-originated component Download PDF

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JP2009161898A
JP2009161898A JP2008316942A JP2008316942A JP2009161898A JP 2009161898 A JP2009161898 A JP 2009161898A JP 2008316942 A JP2008316942 A JP 2008316942A JP 2008316942 A JP2008316942 A JP 2008316942A JP 2009161898 A JP2009161898 A JP 2009161898A
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plant
moisture
glove insert
derived
polyurethane resin
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Masanori Uemoto
雅則 上本
Kiyoshi Kawakami
清 川上
Naotaka Nishimura
直隆 西村
Kazuhiro Nakano
和広 中野
Takayuki Koketsu
貴之 纐纈
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Toray Coatex Co Ltd
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Toray Coatex Co Ltd
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Abstract

<P>PROBLEM TO BE SOLVED: To provide a glove insert made of plant-originated components containing plant-originated components enabling decrease in environmental burden owing to a carbon-neutral system, and excellent in waterproof property and moisture permeability. <P>SOLUTION: The glove insert made of plant-originated components is structured as follows: the instep part and the palm part of the glove insert respectively comprise a laminate composed of a moisture-permeable film and a fabric and are bonded together at the peripheral part of the surface at the side of the fabric so as to be formed into a shape along almost the finger shape. The moisture-permeable waterproof film comprises a polyurethane resin film containing 10-80 wt.% of the plant-originated components. <P>COPYRIGHT: (C)2009,JPO&INPIT

Description

本発明は、植物由来成分からなる手袋インサートに関する。より詳細には、手袋のアウターシェル(表地)とインナー(裏地)との中間層として、又はインナーとして、特にスキー、登山、ライディング、ハンティング用途等に用いられ、昨今の地球温暖化対策における環境負荷の低減のために、カーボンニュートラルに寄与する植物由来成分を含有する手袋インサートに関する。   The present invention relates to a glove insert comprising a plant-derived component. More specifically, it is used as an intermediate layer between the outer shell (outer surface) and inner (lining) of the glove, or as an inner layer, especially for skiing, mountain climbing, riding, hunting, etc., and the environmental impact in recent global warming countermeasures It is related with the glove insert containing the plant-derived component which contributes to carbon neutral for the reduction | decrease.

植物由来成分よりなる布帛としては、例えばポリ乳酸樹脂を用いたものが知られている(例えば特許文献1)。   As a fabric made of a plant-derived component, for example, a fabric using a polylactic acid resin is known (for example, Patent Document 1).

しかし、一般スポーツ用、特にスキー、登山、ライディング、ハンティング用途に用いられる手袋インサートやインナーにおいては、植物由来成分を取り入れて、環境負荷を低減しようとした試みはなされていなかった。   However, in glove inserts and inners used for general sports, particularly skiing, mountain climbing, riding and hunting, no attempt has been made to reduce the environmental burden by incorporating plant-derived components.

本発明者らは、上記に鑑みて植物由来成分を使用した手袋インサートの開発を試みたが、植物由来成分のみでは石油由来の原料を使用した場合と同等の耐水圧を付与することは困難であった。また、手袋の着用時の快適性をより向上させるために、手袋インサートに優れた透湿性を付与する要請もあった。
特開2005−307404号公報
In light of the above, the present inventors have attempted to develop a glove insert using a plant-derived component, but it is difficult to impart a water pressure equivalent to that when using a petroleum-derived raw material alone with a plant-derived component. there were. There has also been a demand for imparting excellent moisture permeability to the glove insert in order to further improve the comfort when wearing gloves.
JP-A-2005-307404

本発明は、上記に鑑みてなされたものであり、アウターシェル(表地)とインナー(裏地)との中間層として、又はインナーとして用いられる手袋インサートであって、カーボンニュートラルによる環境負荷低減可能な植物由来成分を含有してなり、防水性及び透湿性を優れた手袋インサートを提供することも課題とする。   The present invention has been made in view of the above, and is a glove insert used as an intermediate layer between an outer shell (outer surface) and an inner (lining) or as an inner, and can reduce the environmental load due to carbon neutral. It is another object of the present invention to provide a glove insert containing a derived component and having excellent waterproofness and moisture permeability.

本発明者は、鋭意検討の結果、植物由来成分を10〜80%(重量%、以下同様)含有するポリウレタン樹脂膜を使用することにより、環境負荷低減のためのカーボンニュートラルを実現でき、特にポリウレタン樹脂のポリオール成分としてヒマシ油系ポリオールを主体として合成することにより、石油系のポリオールよりなるポリウレタン樹脂膜と同等の性能を有する防水層が得られることを見出し、本発明の完成に至った。   As a result of intensive studies, the present inventor can realize carbon neutral for reducing environmental load by using a polyurethane resin film containing 10 to 80% (% by weight, the same applies hereinafter) of plant-derived components, particularly polyurethane. By synthesizing mainly a castor oil-based polyol as a polyol component of the resin, it was found that a waterproof layer having performance equivalent to that of a polyurethane resin film made of petroleum-based polyol can be obtained, and the present invention has been completed.

すなわち、本発明の手袋インサートは、甲部と掌部とがそれぞれ透湿防水膜と布帛との積層体からなり、前記布帛側の面の周縁部において接着剤によって張り合わされて、ほぼ指の形に沿う形状に形成された手袋インサートであって、前記透湿防水膜が植物由来成分を10〜80重量%含有するポリウレタン樹脂膜からなるものとする。   That is, in the glove insert of the present invention, the upper part and the palm part are each composed of a laminated body of a moisture permeable waterproof membrane and a fabric, and are bonded to each other at the peripheral part of the surface on the fabric side by an adhesive so as to be almost finger-shaped. The moisture permeable waterproof membrane is made of a polyurethane resin membrane containing 10 to 80% by weight of plant-derived components.

ポリウレタン樹脂を構成するポリオール成分としてはヒマシ油ジオールを好適に用いることができる。   As the polyol component constituting the polyurethane resin, castor oil diol can be suitably used.

上記ヒマシ油ジオールはヒマシ油系ポリエーテルポリエステルジオールであって、平均水酸基数が1.8〜2.1個であり、水酸基価が41〜85mgKOH/gであることが好ましい。   The castor oil diol is a castor oil-based polyether polyester diol having an average number of hydroxyl groups of 1.8 to 2.1 and a hydroxyl value of 41 to 85 mgKOH / g.

上記植物由来成分を10〜80重量%含有するポリウレタン樹脂膜は、湿式膜成形技法により形成された多孔膜であって、透湿防水膜を積層した布帛の耐水圧が10kPa以上であり、透湿度がJIS 1099 A−1法で2,000g/m・24H以上であるものとすることができる。 The polyurethane resin film containing 10 to 80% by weight of the plant-derived component is a porous film formed by a wet film forming technique, and the water pressure resistance of the fabric laminated with the moisture-permeable waterproof film is 10 kPa or more, Is 2,000 g / m 2 · 24H or more according to JIS 1099 A-1.

上記植物由来成分を10〜80重量%含有するポリウレタン樹脂膜は、あるいは乾式膜成形技法により形成された無孔膜であって、透湿防水膜を積層した布帛の耐水圧が10kPa以上であり、透湿度がJIS 1099 B−1法で2,000g/m・24H以上であるものとすることができる。 The polyurethane resin film containing 10 to 80% by weight of the plant-derived component is a nonporous film formed by a dry film molding technique, and the water pressure resistance of the fabric laminated with a moisture permeable waterproof film is 10 kPa or more, The moisture permeability may be 2,000 g / m 2 · 24H or more according to JIS 1099 B-1.

植物由来成分の含有量は25〜65重量%であることがより好ましい。   The content of the plant-derived component is more preferably 25 to 65% by weight.

上記甲部と掌部とが接着剤によって張り合わされた接着部の巾は1〜5mmであることが好ましい。   It is preferable that the width | variety of the adhesion part by which the said upper part and the palm part were bonded together by the adhesive agent is 1-5 mm.

上記甲部と掌部とを張り合わせた接着部分は10kPa以上の耐水圧を有することが好ましい。   It is preferable that the bonded portion where the upper portion and the palm portion are bonded has a water pressure resistance of 10 kPa or more.

上記布帛はタテ又はヨコのいずれかにおいて100%以上の伸度を有することが好ましい。   The fabric preferably has an elongation of 100% or more in either length or width.

本発明によれば、植物由来成分を所定量含有することにより、環境負荷低減のためのカーボンニュートラルを実現でき、かつ石油系のポリオールよりなるポリウレタン樹脂膜を用いた場合と同等の防水性及び透湿性を有する、快適性の高い手袋インサートを提供することが可能になる。   According to the present invention, by containing a predetermined amount of plant-derived components, carbon neutral for reducing environmental impact can be realized, and waterproofness and permeability equivalent to those when using a polyurethane resin film made of petroleum-based polyol are used. It becomes possible to provide a highly comfortable glove insert having moisture.

以下、本発明の手袋インサートの詳細について説明する。   Hereinafter, details of the glove insert of the present invention will be described.

本発明において用いられるポリウレタン樹脂膜は、生分解可能なものとするために植物由来成分を主体として合成するものとし、植物由来成分は環境負荷低減の観点からはより多いほうが好ましいが、実用可能なポリウレタン樹脂とするために、下限10%、上限80%とする。環境負荷低減とポリウレタン樹脂の性能との兼ね合いを考慮すると、25〜65%が好ましい。   The polyurethane resin film used in the present invention is synthesized mainly with plant-derived components in order to be biodegradable, and the plant-derived components are more preferable from the viewpoint of reducing environmental burden, but are practical. In order to obtain a polyurethane resin, the lower limit is 10% and the upper limit is 80%. Considering the balance between environmental load reduction and the performance of the polyurethane resin, 25 to 65% is preferable.

特に、ポリウレタン樹脂のポリオール成分としてヒマシ油ジオールを主として用い、かつポリウレタン樹脂を湿式製膜することにより多孔質の透湿性膜が得られ、これを防水層とすることにより、透湿性をも有する手袋インサートが得られる。   In particular, castor oil diol is mainly used as a polyol component of a polyurethane resin, and a porous moisture-permeable film is obtained by wet-forming a polyurethane resin, and a glove having moisture permeability is obtained by using this as a waterproof layer. An insert is obtained.

なお、ヒマシ油系ポリオールの原料であるヒマシ油1kg当りの炭酸ガス吸収量は、16kg(日本熱帯農業学会第94回講演会「ヒマにおける乾物生産およびその分配に及ぼす栽培密度の影響、並びにCO吸収量および太陽エネルギー利用効率」(平成15年9月)の推算による)であり、カーボンニュートラルの点で有用性が高い。ちなみに、カーボンニュートラルの代表的なポリ乳酸の炭酸ガス吸収量は、1.83kg(炭酸ガス排出量=炭酸ガス吸収量として)、また、ケフナの炭酸ガス吸収量は1.5kgであるので、ヒマシ油の吸収力は格段に大きい。 Carbon dioxide absorption per kg of castor oil, which is a raw material of castor oil-based polyol, was 16 kg (94th Lecture Meeting of the Tropical Agriculture Society of Japan “Effect of Cultivation Density on Dry Matter Production and Distribution, and CO 2 "Absorption amount and solar energy utilization efficiency" (September 2003)), and is highly useful in terms of carbon neutrality. Incidentally, the carbon dioxide absorption of carbon neutral neutral polylactic acid is 1.83 kg (as carbon dioxide emission = carbon dioxide absorption), and the carbon dioxide absorption of kefna is 1.5 kg. The oil absorption is much greater.

ヒマシ油は、主に次式で表されるリシノレイン酸のトリグリセライドである。

Figure 2009161898
Castor oil is a triglyceride of ricinoleic acid represented mainly by the following formula.
Figure 2009161898

また、リシノレイン酸は次式で表される構造を有する化合物である。

Figure 2009161898
In addition, ricinoleic acid is a compound having a structure represented by the following formula.
Figure 2009161898

本発明でいうヒマシ油ジオールとはヒマシ油に由来するジオールであり、中でもヒマシ油系ポリエーテルポリエステルジオールであって、平均水酸基数が1.8〜2.1個であり、水酸基価が41〜85mgKOH/gであるものが好ましく、特に平均水酸基数が1.95〜2.05個のものを好適に用いることができる。水酸基数が2.1個を越えると3価のポリオールの分枝あるいは架橋構造の生成のために、樹脂膜を形成するためのコーティングに適したポリウレタン樹脂を得ることが困難となる。すなわち、本発明で用いるウレタン樹脂は、構造が線状であり、分枝あるいは架橋構造をあまり持たず、布帛にコーティング可能な溶液の粘性を持つことが好ましい。分枝構造が増加すると粘性が大きくなり、コーティングに適さなくなる。また、架橋構造になると極微量でも粘性変化が起こり、少量でも粘性変化が大きく、さらに架橋量が増加するとウレタン樹脂溶液を得ることができなくなる。   The castor oil diol as referred to in the present invention is a diol derived from castor oil, among which castor oil-based polyether polyester diol has an average number of hydroxyl groups of 1.8 to 2.1, and a hydroxyl value of 41 to 41. Those having 85 mg KOH / g are preferred, and those having an average number of hydroxyl groups of 1.95 to 2.05 can be suitably used. When the number of hydroxyl groups exceeds 2.1, it is difficult to obtain a polyurethane resin suitable for coating for forming a resin film because of the generation of a trivalent polyol branch or crosslinked structure. That is, it is preferable that the urethane resin used in the present invention has a linear structure, has little branching or cross-linking structure, and has a solution viscosity that can be coated on a fabric. Increasing the branch structure increases the viscosity and makes it unsuitable for coating. Moreover, when it becomes a crosslinked structure, the viscosity change occurs even in a very small amount, the viscosity change is large even in a small amount, and if the amount of crosslinking further increases, a urethane resin solution cannot be obtained.

上記植物由来成分を含有するポリウレタン樹脂を得るための方法としては、例えば、ジメチルホルムアミド(DMF)やジメチルスルホキシド(DMSO)等に代表される極性溶剤や、メチルエチルケトン(MEK)、トルエン、キシレン等の溶剤に、ヒマシ油ジオール等の2価の植物由来ポリオールを溶解し、ここに2価のイソシアネート(ヘキサメチレンジイソシアネート、イソホロンジイソシアネート、ジフェニルメタンジイソシアネート(MDI)、水添MDIなど)を添加し、充分に反応させ、末端にイソシアネートまたは、水酸基を有するプレポリマーを調製したのち、ジオール(石油由来のエチレングリコール、プロピレングリコール、ブチレングリコール等、植物由来の1,3−プロパンジオール、1,2−ヘキサンジオール等)、又は2価のイソシアネート(ヘキサメチレンジイソシアネート、イソホロンジイソシアネート、ジフェニルメタンジイソシアネート(MDI)、水添MDIなど)を添加し、鎖長延長反応で重合度を上げる方法を用いることができる。   Examples of a method for obtaining a polyurethane resin containing plant-derived components include polar solvents such as dimethylformamide (DMF) and dimethyl sulfoxide (DMSO), and solvents such as methyl ethyl ketone (MEK), toluene, and xylene. In addition, a divalent plant-derived polyol such as castor oil diol is dissolved, and divalent isocyanate (hexamethylene diisocyanate, isophorone diisocyanate, diphenylmethane diisocyanate (MDI), hydrogenated MDI, etc.) is added thereto and allowed to react sufficiently. After preparing a prepolymer having an isocyanate or a hydroxyl group at the terminal, a diol (petroleum-derived ethylene glycol, propylene glycol, butylene glycol, etc., plant-derived 1,3-propanediol, 1,2-hexanediol, Etc.), or a divalent isocyanate was added (hexamethylene diisocyanate, isophorone diisocyanate, diphenylmethane diisocyanate (MDI), and hydrogenated MDI), it is possible to use a method of increasing the polymerization degree of a chain extending reaction.

上記において、2価の植物由来ポリオールと2価のイソシアネートとを反応させてプレポリマーを形成する際には、必要に応じて、2価の植物由来ポリオールに加えて、それ以外のポリオール、例えばポリエステルポリオール、ポリエーテルポリオールを共重合することも可能である。より具体的には、2価の石油由来のポリオールである、ポリエチレンアジペート、ポリブチレンアジペート、ポリカプロラクトンジオール、ポリエチレングリコール、ポリプロピレングリコール、ポリテトラメチレングリコール等が共重合可能である。あるいはポリカーボネートポリオール、シリコーン系ポリオール、フッ素系ポリオール、ポリアミド系ポリオール等を共重合して用いることもできる。これら植物由来ポリオール以外のポリオールはポリオール全量中50重量%(固形分比)以下の割合で混合可能であるが、植物由来比率を低減しないためにも、混合量は25重量%(固形分比)以下であることが望ましい。   In the above, when a prepolymer is formed by reacting a divalent plant-derived polyol and a divalent isocyanate, if necessary, in addition to the divalent plant-derived polyol, other polyols such as polyesters are used. It is also possible to copolymerize polyols and polyether polyols. More specifically, divalent petroleum-derived polyols such as polyethylene adipate, polybutylene adipate, polycaprolactone diol, polyethylene glycol, polypropylene glycol, and polytetramethylene glycol can be copolymerized. Alternatively, polycarbonate polyol, silicone polyol, fluorine polyol, polyamide polyol and the like can be copolymerized and used. Polyols other than these plant-derived polyols can be mixed in a proportion of 50% by weight (solid content ratio) or less in the total amount of polyol, but the mixing amount is 25% by weight (solid content ratio) in order not to reduce the plant-derived ratio. The following is desirable.

しかし、植物由来成分を含有するポリウレタン樹脂の重合方法については、これらの方法に特に限定されるものではない。   However, the method for polymerizing a polyurethane resin containing a plant-derived component is not particularly limited to these methods.

透湿性を有する防水層を得るには、例えば植物由来成分を含有するポリウレタン樹脂から湿式膜成形技法(以下、湿式法と記載する)により微多孔質膜を得る方法が用いられる。また、植物由来成分を含有するポリウレタン樹脂を重合する際に、ポリエチレングリコールよりなるポリオールを共重合することにより、乾式法により透湿性を有する無孔膜を得ることもできる。   In order to obtain a waterproof layer having moisture permeability, for example, a method of obtaining a microporous membrane from a polyurethane resin containing a plant-derived component by a wet membrane molding technique (hereinafter referred to as a wet method) is used. Moreover, when polymerizing the polyurethane resin containing a plant-derived component, a nonporous film having moisture permeability can be obtained by a dry method by copolymerizing a polyol made of polyethylene glycol.

より具体的には、植物由来成分を含有するポリウレタン樹脂を水に可溶な極性溶剤(DMF、DMSO等)に溶解してなるポリウレタン樹脂溶液を離型布等にコーティングし、これを水中あるいは、極性溶媒を含有する水溶液中で湿式ゲル化させることにより透湿性と防水性とを併せ持つ微多孔質膜を形成することができる。   More specifically, a polyurethane resin solution obtained by dissolving a polyurethane resin containing a plant-derived component in a water-soluble polar solvent (DMF, DMSO, etc.) is coated on a release cloth, etc. A microporous membrane having both moisture permeability and waterproofness can be formed by wet gelation in an aqueous solution containing a polar solvent.

あるいは、植物由来成分を含有するポリウレタン樹脂の合成の際にオキシエチレン基含有高分子ジオールを共重合することにより透湿性のポリウレタン樹脂とし、これを溶解する溶剤で溶解してなるポリウレタン樹脂溶液を離型紙等にコーティングし、この溶剤を乾燥させて透湿性と防水性を併せ持つ無孔質膜を形成する方法等がある。   Alternatively, when a polyurethane resin containing a plant-derived component is synthesized, an oxyethylene group-containing polymer diol is copolymerized to form a moisture-permeable polyurethane resin, and a polyurethane resin solution obtained by dissolving the polyurethane resin solution in a solvent that dissolves the polyurethane resin solution is separated. There is a method of forming a non-porous film having both moisture permeability and waterproof properties by coating on a pattern paper or the like and drying this solvent.

また、ポリウレタン樹脂に透湿性を付与するためには、2価のポリオールとして、オキシエチレン基含有高分子ジオール以外に、例えばポリエチレングリコール(以下PEGと略記)、ポリオキシエチレンオキシプロピレンブロックもしくはランダム共重合ジオール、ポリオキシエチレンオキシテトラメチレンブロックもしくはランダム共重合ジオール;エチレングリコール、プロピレングリコール、1,4−ブタンジオール、1,6−ヘキサメチレングリコール、ビス(ヒドロキシメチル)シクロヘキサン、4,4’−ビス(2−ヒドロキシエトキシ)−ジフェニルプロパンなどの低分子グリコールのエチレンオキシド付加物;分子量1000以下のPEGとジカルボン酸(例えばコハク酸、アジピン酸、セバシン酸、テレフタル酸、イソフタル酸など)とを反応させて得られる縮合ポリエーテルエステルジオール、又はこれらの2種以上の混合物を用いることもできる。   In order to impart moisture permeability to the polyurethane resin, in addition to the oxyethylene group-containing polymer diol, for example, polyethylene glycol (hereinafter abbreviated as PEG), polyoxyethylene oxypropylene block or random copolymer as a divalent polyol. Diol, polyoxyethyleneoxytetramethylene block or random copolymer diol; ethylene glycol, propylene glycol, 1,4-butanediol, 1,6-hexamethylene glycol, bis (hydroxymethyl) cyclohexane, 4,4′-bis ( Ethylene oxide adducts of low molecular weight glycols such as 2-hydroxyethoxy) -diphenylpropane; PEG with a molecular weight of 1000 or less and dicarboxylic acids (eg succinic acid, adipic acid, sebacic acid, terephthalic acid, iso Condensation polyetherester diols obtained by reacting the like Tal acid), or may also be used a mixture of two or more thereof.

植物由来成分を含有するポリウレタン樹脂の重合については、これらの方法に特に限定されるものではない。   The polymerization of the polyurethane resin containing a plant-derived component is not particularly limited to these methods.

上記ポリウレタン樹脂には、必要に応じて、シリカ微粉末、撥水剤、顔料、マット剤、機能付与剤(消臭、抗菌等)等の添加剤を適宜添加することもできる。   If necessary, additives such as silica fine powder, water repellent, pigment, matting agent, function-imparting agent (deodorant, antibacterial agent, etc.) can also be added to the polyurethane resin.

本発明の植物由来成分を含有するポリウレタン膜の透湿防水膜を積層した布帛の製造方法としては、布帛に樹脂溶液を直接コーティングしてもよく、あるいは、離型布、離型紙にコーティング等で形成した透湿防水膜を布帛に接着剤を用いて積層することできるが、これらに限定されない。   As a method for producing a fabric laminated with a moisture permeable waterproof membrane of a polyurethane membrane containing a plant-derived component of the present invention, a resin solution may be directly coated on the fabric, or a release cloth, a release paper may be coated, etc. The formed moisture permeable waterproof membrane can be laminated on the fabric using an adhesive, but is not limited thereto.

コーティング方法としては、ナイフコーティング、ナイフオーバーロールコーティング、リバースロールコーティングなどの各種のコーティング方法が適宜使用できる。   As a coating method, various coating methods such as knife coating, knife over roll coating, and reverse roll coating can be appropriately used.

上記透湿防水膜は、実用上の防水性能の点から耐水圧が10kPa以上であることが好ましい。   The moisture-permeable waterproof membrane preferably has a water pressure resistance of 10 kPa or more from the viewpoint of practical waterproof performance.

また、上記透湿防水層は、透湿度としてA−1法で2,000g/m・24hrs以上、もしくは、B−1法で2,000g/m・24hrs以上を有することが望ましい。 Further, the moisture-permeable waterproof layer is moisture permeability as in Method A-1 2,000g / m 2 · 24hrs or more, or, it is desirable to have a more 2,000g / m 2 · 24hrs at B-1 method.

布帛への積層は、透湿性を有する接着剤による全面接着や、あるいは透湿性の有無に関らず、グラビア塗布等によるドット接着等により行うことができる。   Lamination to the fabric can be performed by whole surface adhesion with a moisture-permeable adhesive, or dot adhesion by gravure coating or the like regardless of the presence or absence of moisture permeability.

手袋インサートの甲部および掌部の布帛面と布帛面とを貼り合せる接着剤としては、二液硬化型接着剤、ホットメルト型接着剤などが挙げられるが、その作業性を考慮に入れるとホットメルト型接着剤を使用することが好ましく、材質としてはポリウレタン、アクリルなどが挙げられ、風合いの良さの点からはポリウレタンを使用することが好ましい。熱プレスを行う際、あまり温度をかけすぎると布帛および透湿防水膜に損傷を与えてしまい好ましくないため、接着剤として使用するホットメルト性を有するポリウレタンの融点は70〜150℃であることが好ましく、さらに好ましくは80〜120℃である。   Examples of the adhesive that bonds the fabric surface of the back and palm of the glove insert to each other include a two-component curable adhesive, a hot-melt adhesive, and the like. It is preferable to use a melt-type adhesive, and examples of the material include polyurethane and acrylic. From the viewpoint of good texture, it is preferable to use polyurethane. When performing hot pressing, if the temperature is too high, the fabric and the moisture-permeable waterproof membrane are damaged, which is not preferable. Therefore, the melting point of the polyurethane having hot melt property used as an adhesive is 70 to 150 ° C. Preferably, it is 80-120 degreeC.

また、手袋インサートの甲部および掌部の布帛面と布帛面とを手形状に塗工した接着剤にて貼り合わせる際、その接着巾が狭いと接着強度が弱く、手袋縫製時および手袋着用時にインサートが破損するため好ましくない。また、接着巾が広すぎると手袋完成品および手袋インサート着用時に接着部が指に当たり、着用感が不快なものとなるため好ましくない。これらのことから、手形状に塗工した接着剤の巾は1〜5mmであることが好ましく、さらに好ましくは2〜4mmとする。   Also, when the fabric surface and fabric surface of the back and palm of the glove insert are bonded together with an adhesive coated in a hand shape, the adhesive strength is weak if the adhesive width is narrow, when sewing gloves and wearing gloves This is not preferable because the insert is damaged. Also, if the adhesive width is too wide, the adhesive part hits the finger when wearing the finished glove product and the glove insert, and the feeling of wearing becomes unpleasant, which is not preferable. From these things, it is preferable that the width | variety of the adhesive agent applied to the hand shape is 1-5 mm, More preferably, you may be 2-4 mm.

手袋インサートにおいて甲部および掌部の貼り合せ箇所の耐水圧が低いものであれば、手袋として着用したとき、雨天時等手袋が水に濡れた際手袋内部にまで水が浸入してくるため好ましくない。このことから、甲部および掌部の接着部分の耐水圧が10kPa以上であることが好ましく、さらに防水性を高めるためには耐水圧が30kPa以上であることがより好ましい。   If the glove insert has a low water pressure at the bonding part of the upper part and the palm part, it is preferable because the water penetrates into the glove when it gets wet when it is wet. Absent. From this, it is preferable that the water pressure resistance of the bonded portion of the upper part and the palm part is 10 kPa or more, and more preferably, the water pressure resistance is 30 kPa or more in order to improve waterproofness.

手袋インサートの甲部および掌部の布帛は、伸度の高いタテ編、丸編であることが、手入れ感、フィット性の点より好ましく、タテあるいはヨコのいずれかが100%以上の伸度を有することが好ましい。しかしながら、伸度が高ければ、編物に限定されるものではない。   The fabric of the upper part and palm part of the glove insert is preferably a warp knitting or a circular knitting having a high degree of elongation from the viewpoint of care and fit, and either the warp or the width has an elongation of 100% or more. It is preferable to have. However, it is not limited to a knitted fabric as long as the elongation is high.

布帛の素材は、特に限定されないが、例えばナイロン、ポリエステルの加工糸使いの伸度の高い編物が好適に使用できる。   The material of the fabric is not particularly limited, but, for example, a knitted fabric with high elongation using a processed yarn of nylon or polyester can be suitably used.

以下、本発明を実施例で詳細に説明するが本発明はこれらに限定されるものではない。   EXAMPLES Hereinafter, although an Example demonstrates this invention in detail, this invention is not limited to these.

なお、以下において耐水圧及び透湿度の測定方法としては次のものを用いた;
(1)耐水圧:JIS規格L1092
(2)透湿度:JIS規格L1099のA−1、B−1法
In addition, the following was used as a measuring method of water pressure resistance and moisture permeability in the following;
(1) Water pressure resistance: JIS standard L1092
(2) Moisture permeability: A-1 and B-1 methods of JIS standard L1099

〈植物由来ポリウレタン樹脂25%溶液1〉
ヒマシ油ジオール1(伊藤製油(株)製、PH−5002、平均水酸基数:2.03個、水酸基価:43mgKOH/g)25gとヒマシ油ジオール2(伊藤製油(株)製、H−56、平均水酸基数:2.03個、水酸基価:83mgKOH/g)25g、ポリブチレンアジペート(日本ポリウレタン(株)製、ニッポランN−4060)50g、及びDMF250gを1リットルのセパラブルコルベンに入れて溶解し、45℃に調温しながらMDI56.1gを添加し、おおよそ1時間、45℃で反応させ、プレポリマーとした。この後温度を60℃に昇温し、エチレングリコール10.7gを添加し、60℃で鎖長延長反応をさせ、粘度上昇に合せてDMF250gを分割添加しながら重合を行った。約8時間で重合が終わり、植物由来率30.0%(固形分中比率)のポリウレタン樹脂25%溶液が得られた。
<Plant-derived polyurethane resin 25% solution 1>
Castor oil diol 1 (produced by Ito Oil Co., Ltd., PH-5002, average number of hydroxyl groups: 2.03, hydroxyl value: 43 mg KOH / g) and castor oil diol 2 (produced by Ito Oil Co., Ltd., H-56) Average number of hydroxyl groups: 2.03, hydroxyl value: 83 mg KOH / g) 25 g, polybutylene adipate (manufactured by Nippon Polyurethane Co., Ltd., Nipponporan N-4060) and DMF 250 g were dissolved in 1 liter separable colben. While adjusting the temperature to 45 ° C., 56.1 g of MDI was added, and the mixture was reacted at 45 ° C. for about 1 hour to obtain a prepolymer. Thereafter, the temperature was raised to 60 ° C., 10.7 g of ethylene glycol was added, a chain extension reaction was carried out at 60 ° C., and polymerization was carried out while 250 g of DMF was added in portions as the viscosity increased. Polymerization was completed in about 8 hours, and a 25% polyurethane resin solution having a plant-derived rate of 30.0% (solid content ratio) was obtained.

〈植物由来ポリウレタン樹脂25%溶液2〉
ヒマシ油ジオール1(伊藤製油(株)製、PH−5002、平均水酸基数:2.03個、水酸基価:43mgKOH/g)40gとヒマシ油ジオール2(伊藤製油(株)製、H−56、平均水酸基数:2.03個、水酸基価:83mgKOH/g)40g、ポリブチレンアジペート(日本ポリウレタン(株)製、ニッポランN−4060)20g及びDMF250gを1リットルのセパラブルコルベンに入れて溶解し、45℃に調温しながらMDI57.6gを添加し、おおよそ1時間、45℃で反応させ、プレポリマーとした。この後温度を60℃に昇温し、エチレングリコール10.9gを添加し、60℃で鎖長延長反応をさせ、粘度上昇に合せてDMF256gを分割添加しながら重合を行った。約8時間で重合が終わり、植物由来率47.5%(固形分中比率)のポリウレタン樹脂25%溶液が得られた。
<Plant-derived polyurethane resin 25% solution 2>
Castor oil diol 1 (Ito Oil Co., Ltd., PH-5002, average number of hydroxyl groups: 2.03, hydroxyl value: 43 mg KOH / g) 40 g and castor oil diol 2 (Ito Oil Co., Ltd., H-56, Average number of hydroxyl groups: 2.03, hydroxyl value: 83 mg KOH / g) 40 g, polybutylene adipate (manufactured by Nippon Polyurethane Co., Ltd., NIPPOLAN N-4060) and DMF 250 g were dissolved in 1 liter separable colben, While adjusting the temperature to 45 ° C., 57.6 g of MDI was added, and the mixture was allowed to react at 45 ° C. for about 1 hour to obtain a prepolymer. Thereafter, the temperature was raised to 60 ° C., 10.9 g of ethylene glycol was added, a chain extension reaction was carried out at 60 ° C., and polymerization was carried out while adding 256 g of DMF in portions as the viscosity increased. Polymerization was completed in about 8 hours, and a 25% polyurethane resin solution having a plant-derived rate of 47.5% (ratio in solid content) was obtained.

〈植物由来ポリウレタン樹脂25%溶液3〉
ヒマシ油ジオール1(伊藤製油(株)製、PH−5002、平均水酸基数:2.03個、水酸基価:43mgKOH/g)50gとヒマシ油ジオール2(伊藤製油(株)製、H−56、平均水酸基数:2.03個、水酸基価:83mgKOH/g)50g、及びDMF250gを1リットルのセパラブルコルベンに入れて溶解し、45℃に調温しながらMDI58.6gを添加し、おおよそ1時間、45℃で反応させ、プレポリマーとした。この後温度を60℃に昇温し、エチレングリコール10.9gを添加し、60℃で鎖長延長反応をさせ、粘度上昇に合せてDMF259gを分割添加しながら重合を行った。約8時間で重合が終わり、植物由来率58.9%(固形分中比率)のポリウレタン樹脂25%溶液が得られた。
<Plant-derived polyurethane resin 25% solution 3>
Castor oil diol 1 (Ito Oil Co., Ltd., PH-5002, average number of hydroxyl groups: 2.03, hydroxyl value: 43 mgKOH / g) and castor oil diol 2 (Ito Oil Co., Ltd., H-56, Average number of hydroxyl groups: 2.03, hydroxyl value: 83 mg KOH / g) 50 g and DMF 250 g were dissolved in 1 liter of separable colben, and MDI 58.6 g was added while adjusting the temperature to 45 ° C., approximately 1 hour , Reacted at 45 ° C. to obtain a prepolymer. Thereafter, the temperature was raised to 60 ° C., 10.9 g of ethylene glycol was added, a chain extension reaction was carried out at 60 ° C., and polymerization was carried out while adding 259 g of DMF in portions as the viscosity increased. Polymerization was completed in about 8 hours, and a 25% polyurethane resin solution having a plant-derived rate of 58.9% (ratio in solid content) was obtained.

〈植物由来ポリウレタン樹脂25%溶液4〉
ヒマシ油ジオール1(伊藤製油(株)製、PH−5002、平均水酸基数:2.03個、水酸基価:43mgKOH/g)80gとヒマシ油ジオール2(伊藤製油(株)製、H−56、平均水酸基数:2.03個、水酸基価:83mgKOH/g)20g、及びDMF220gを1リットルのセパラブルコルベンに入れて溶解し、45℃に調温しながらMDI48.7gを添加し、おおよそ1時間、45℃で反応させ、プレポリマーとした。この後温度を60℃に昇温し、エチレングリコール9.2gを添加し、60℃で鎖長延長反応をさせ、粘度上昇に合せてDMF254gを分割添加しながら重合を行った。約8時間で重合が終わり、植物由来率63.3%(固形分中比率)のポリウレタン樹脂25%溶液が得られた。
<Plant-derived polyurethane resin 25% solution 4>
Castor oil diol 1 (manufactured by Ito Oil Co., Ltd., PH-5002, average number of hydroxyl groups: 2.03, hydroxyl value: 43 mgKOH / g) and castor oil diol 2 (manufactured by Ito Oil Co., Ltd., H-56, Average number of hydroxyl groups: 2.03, hydroxyl value: 83 mg KOH / g) 20 g and DMF 220 g were dissolved in 1 liter of separable colben, and MDI 48.7 g was added while adjusting the temperature to 45 ° C., approximately 1 hour , Reacted at 45 ° C. to obtain a prepolymer. Thereafter, the temperature was raised to 60 ° C., 9.2 g of ethylene glycol was added, a chain extension reaction was carried out at 60 ° C., and polymerization was carried out while adding 254 g of DMF in proportion to the increase in viscosity. Polymerization was completed in about 8 hours, and a 25% polyurethane resin solution having a plant-derived rate of 63.3% (ratio in solid content) was obtained.

〈植物由来透湿性ポリウレタン樹脂30%溶液1〉
攪拌機および温度計を備えた1L四つ口フラスコに乾燥窒素雰囲気下にて、ヒマシ油ジオール2(伊藤製油(株)製、H−56、平均水酸基数:2.03個、水酸基価:83mgKOH/g)12gとヒマシ油ジオール1(伊藤製油(株)製、PH−5002、平均水酸基数:2.03個、水酸基価:43mgKOH/g)8gと、ポリオキシエチレンンジオール(第一工業(株)製、D−300W)80gとDMF150gを仕込み、攪拌し、均一に溶解させた。50℃の温度調節下、MDI7.2gを投入し、1時間反応させた後、さらにMDI55.8gを添加し、プレポリマー最終反応を50℃で0.5時間行った。続いてエチレングリコール13.4gをDMF50gと混合し、添加後、60℃に昇温し、鎖長延長反応を行った。途中粘度上昇を見ながらDMF212gを分割添加しつつ8時間反応させて、固形分中植物由来成分含有比率11.3%、オキシエチレン基含有比率は36.3%のポリウレタン樹脂30%溶液が得られた。
<Plant-derived moisture-permeable polyurethane resin 30% solution 1>
In a 1 L four-necked flask equipped with a stirrer and a thermometer, castor oil diol 2 (manufactured by Ito Oil Co., Ltd., H-56, average number of hydroxyl groups: 2.03, hydroxyl value: 83 mgKOH / g) 12 g, castor oil diol 1 (manufactured by Ito Oil Co., Ltd., PH-5002, average number of hydroxyl groups: 2.03, hydroxyl value: 43 mg KOH / g), 8 g of polyoxyethylene diol (Daiichi Kogyo Co., Ltd.) ), D-300W) 80 g and DMF 150 g were charged, stirred and dissolved uniformly. Under temperature control of 50 ° C., 7.2 g of MDI was added and reacted for 1 hour, and then 55.8 g of MDI was further added, and the prepolymer final reaction was performed at 50 ° C. for 0.5 hour. Subsequently, 13.4 g of ethylene glycol was mixed with 50 g of DMF, and after addition, the temperature was raised to 60 ° C. to conduct a chain extension reaction. While observing the increase in viscosity on the way, 212 g of DMF was added in portions and reacted for 8 hours to obtain a 30% polyurethane resin solution containing 11.3% plant-derived component in solids and 36.3% oxyethylene group. It was.

〈植物由来透湿性ポリウレタン樹脂30%溶液2〉
攪拌機および温度計を備えた1L四つ口フラスコにヒマシ油ジオール2(伊藤製油(株)製、H−56、平均水酸基数:2.03個、水酸基価:83mgKOH/g)30gと、ヒマシ油ジオール1(伊藤製油(株)製、PH−5002、平均水酸基数:2.03個、水酸基価:43mgKOH/g)20gと、ポリオキシエチレンンジオール(第一工業(株)製、D−300W)50gと、DMF150gを仕込み、均一に溶解させた。50℃の温度調節下、MDI10.2gを投入し、1時間反応させた後、MDI52.8gを添加し、プレポリマー最終反応を50℃で0.5時間行った。続いてエチレングリコール12.8gをDMF50gと混合し添加後、60℃に昇温し鎖長延長反応を行った。途中粘度上昇を見ながらDMF210gを分割添加しながら8時間反応させて、固形分中植物由来成分含有比率28.4%、オキシエチレン基含有比率は22.8%のポリウレタン樹脂30%溶液が得られる。
<Plant-derived moisture-permeable polyurethane resin 30% solution 2>
Castor oil diol 2 (manufactured by Ito Oil Co., Ltd., H-56, average number of hydroxyl groups: 2.03, hydroxyl value: 83 mgKOH / g) and castor oil in a 1 L four-necked flask equipped with a stirrer and a thermometer Diol 1 (produced by Ito Oil Co., Ltd., PH-5002, average number of hydroxyl groups: 2.03, hydroxyl value: 43 mg KOH / g) 20 g and polyoxyethylene diol (Daiichi Kogyo Co., Ltd., D-300W) ) 50 g and DMF 150 g were charged and dissolved uniformly. Under temperature control of 50 ° C., 10.2 g of MDI was added and reacted for 1 hour, and then 52.8 g of MDI was added, and the prepolymer final reaction was performed at 50 ° C. for 0.5 hour. Subsequently, 12.8 g of ethylene glycol was mixed with 50 g of DMF and added, and then the temperature was raised to 60 ° C. to carry out a chain extension reaction. The reaction was performed for 8 hours while adding 210 g of DMF while observing the increase in viscosity in the middle, and a 30% polyurethane resin solution having a plant-derived component content ratio of 28.4% and an oxyethylene group content ratio of 22.8% in the solid content was obtained. .

〈植物由来透湿性ポリウレタン樹脂30%溶液3〉
攪拌機および温度計を備えた1L四つ口フラスコにヒマシ油ジオール2(伊藤製油(株)製、H−56、平均水酸基数:2.03個、水酸基価:83mgKOH/g)36gと、ヒマシ油ジオール1(伊藤製油(株)製、PH−5002、平均水酸基数:2.03個、水酸基価:43mgKOH/g)24gと、ポリオキシエチレンンジオール(第一工業(株)製、D−300W)40gと、DMF150gを仕込み、均一に溶解させる。50℃の温度調節下、MDI20.5gを投入し、1時間反応させた後、MDI42.5gを添加し、プレポリマー最終反応を50℃で0.5時間行った。続いてエチレングリコール10.0gをDMF50gと混合し、添加後、60℃に昇温し鎖長延長反応を行った。途中粘度上昇を見ながらDMF204gを分割添加しながら8時間反応させて、固形分中植物由来成分含有比率34.7%、オキシエチレン基含有比率は20.8%のポリウレタン樹脂30%溶液が得られた。
<Plant-derived moisture-permeable polyurethane resin 30% solution 3>
Castor oil diol 2 (manufactured by Ito Oil Co., Ltd., H-56, average number of hydroxyl groups: 2.03, hydroxyl value: 83 mgKOH / g) 36 g and castor oil in a 1 L four-necked flask equipped with a stirrer and a thermometer Diol 1 (manufactured by Ito Oil Co., Ltd., PH-5002, average number of hydroxyl groups: 2.03, hydroxyl value: 43 mgKOH / g) 24 g and polyoxyethylene diol (Daiichi Kogyo Co., Ltd., D-300W) 40 g and DMF 150 g are charged and dissolved uniformly. Under a temperature control of 50 ° C., 20.5 g of MDI was added and reacted for 1 hour, and then 42.5 g of MDI was added, and the prepolymer final reaction was performed at 50 ° C. for 0.5 hour. Subsequently, 10.0 g of ethylene glycol was mixed with 50 g of DMF, and after addition, the temperature was raised to 60 ° C. to carry out a chain extension reaction. The reaction was performed for 8 hours while adding 204 g of DMF while observing the increase in viscosity on the way, and a 30% polyurethane resin solution having a plant-derived component content ratio of 34.7% and an oxyethylene group content ratio of 20.8% in the solid content was obtained. It was.

〈植物由来透湿性ポリウレタン樹脂30%溶液4〉
攪拌機および温度計を備えた1L四つ口フラスコにヒマシ油ジオール2(伊藤製油(株)製、H−56、平均水酸基数:2.03個、水酸基価:83mgKOH/g)42gと、ヒマシ油ジオール1(伊藤製油(株)製、PH−5002、平均水酸基数:2.03個、水酸基価:43mgKOH/g)28gと、ポリオキシエチレンンジオール(第一工業(株)製、D−300W)30gと、DMF150gを仕込み、均一に溶解させた。50℃の温度調節下、MDI11.3gを投入し、1時間反応させた後、MDI51.7gを添加し、プレポリマー最終反応を50℃で0.5時間行った。続いてエチレングリコール10.1gと1,3−ブチレングリコール3.5gをDMF50gと混合し、添加後、60℃に昇温し、鎖長延長反応を行う。途中粘度上昇を見ながらDMF204gを分割添加しながら8時間反応させて、固形分中植物由来成分含有比率39.6%、オキシエチレン基含有比率は13.6%のポリウレタン樹脂30%溶液が得られた。
<Plant-derived moisture-permeable polyurethane resin 30% solution 4>
Castor oil diol 2 (manufactured by Ito Oil Co., Ltd., H-56, average number of hydroxyl groups: 2.03, hydroxyl value: 83 mgKOH / g) 42 g and castor oil in a 1 L four-necked flask equipped with a stirrer and a thermometer Diol 1 (Ito Oil Co., Ltd., PH-5002, average number of hydroxyl groups: 2.03, hydroxyl value: 43 mg KOH / g) 28 g and polyoxyethylene diol (Daiichi Kogyo Co., Ltd., D-300W) ) 30 g and DMF 150 g were charged and dissolved uniformly. Under temperature control of 50 ° C., 11.3 g of MDI was added and reacted for 1 hour, then 51.7 g of MDI was added, and the final prepolymer reaction was carried out at 50 ° C. for 0.5 hour. Subsequently, 10.1 g of ethylene glycol and 3.5 g of 1,3-butylene glycol are mixed with 50 g of DMF, and after addition, the temperature is raised to 60 ° C. to carry out a chain extension reaction. The reaction was performed for 8 hours while adding 204 g of DMF while observing the increase in viscosity on the way, and a 30% polyurethane resin solution having a plant-derived component content ratio of 39.6% and an oxyethylene group content ratio of 13.6% in the solid content was obtained. It was.

〈植物由来透湿性ポリウレタン樹脂30%溶液5〉
攪拌機および温度計を備えた1L四つ口フラスコにヒマシ油ジオール2(伊藤製油(株)製、H−56、平均水酸基数:2.03個、水酸基価:83mgKOH/g)48gと、ヒマシ油ジオール1(伊藤製油(株)製、PH−5002、平均水酸基数:2.03個、水酸基価:43mgKOH/g)32gと、ポリオキシエチレンンジオール(第一工業(株)製、D−300W)20gと、DMF150gを仕込み、均一に溶解させた。50℃の温度調節下、MDI11.9gを投入し、1時間反応させた後、MDI51.1gを添加し、プレポリマー最終反応を50℃で0.5時間にて行った。続いてエチレングリコール9.9gと1,3−ブチレングリコール3.5gをDMF50gと混合し、添加後、60℃に昇温し鎖長延長反応を行った。途中粘度上昇を見ながらDMF204gを分割添加しながら8時間反応させて、固形分中植物由来成分含有比率46.3%、オキシエチレン基含有比率は9.3%のポリウレタン樹脂30%溶液が得られた。
<Plant-derived moisture-permeable polyurethane resin 30% solution 5>
Castor oil diol 2 (manufactured by Ito Oil Co., Ltd., H-56, average number of hydroxyl groups: 2.03, hydroxyl value: 83 mgKOH / g) 48 g and castor oil in a 1 L four-necked flask equipped with a stirrer and a thermometer Diol 1 (manufactured by Ito Oil Co., Ltd., PH-5002, average number of hydroxyl groups: 2.03, hydroxyl value: 43 mgKOH / g) 32 g and polyoxyethylene diol (Daiichi Kogyo Co., Ltd., D-300W) ) 20 g and DMF 150 g were charged and dissolved uniformly. Under a temperature control of 50 ° C., 11.9 g of MDI was added and reacted for 1 hour, then 51.1 g of MDI was added, and the final prepolymer reaction was performed at 50 ° C. for 0.5 hour. Subsequently, 9.9 g of ethylene glycol and 3.5 g of 1,3-butylene glycol were mixed with 50 g of DMF, and after addition, the temperature was raised to 60 ° C. to perform a chain extension reaction. The reaction was performed for 8 hours while adding 204 g of DMF while observing the increase in viscosity in the middle, and a 30% polyurethane resin solution having a plant-derived component content ratio of 46.3% and an oxyethylene group content ratio of 9.3% in the solid content was obtained. It was.

〈石油由来ポリウレタン樹脂25%溶液1〉
ポリブチレンアジペート(日本ポリウレタン(株)製、ニッポランN−4060)100gとDMF250gを1リットルのセパラブルコルベンに入れて溶解し、45℃に調温しながらMDI53.6gを添加し、おおよそ1時間、45℃で反応させプレポリマーとした。この後温度を60℃に昇温し、エチレングリコール10.2gを添加し、60℃で鎖長延長反応をさせ、粘度上昇に合せてDMF241gを分割添加しながら重合を行った。約8時間で重合が終わり、石油由来ポリウレタン樹脂25%溶液が得られた。
<Petroleum-derived polyurethane resin 25% solution 1>
100 g of polybutylene adipate (Nippon Polyurethane Co., Ltd., NIPPOLAN N-4060) and 250 g of DMF are dissolved in 1 liter of separable colben, and 53.6 g of MDI is added while adjusting the temperature to 45 ° C. The reaction was conducted at 45 ° C. to obtain a prepolymer. Thereafter, the temperature was raised to 60 ° C., 10.2 g of ethylene glycol was added, a chain extension reaction was carried out at 60 ° C., and polymerization was carried out while adding 241 g of DMF in proportion to the increase in viscosity. The polymerization was completed in about 8 hours, and a 25% petroleum-derived polyurethane resin solution was obtained.

〈石油由来透湿性ポリウレタン樹脂30%溶液2〉
攪拌機および温度計を備えた1L四つ口フラスコにポリエチレンアジペート(日本ポリウレタン(株)製、ニッポランN−4010)60gと、ポリオキシエチレンンジオール(第一工業(株)製、D−300W)40gと、DMF150gを仕込み、均一に溶解させた。50℃の温度調節下、MDI20.5gを投入し、1時間反応させた後、MDI42.5gを添加し、プレポリマー最終反応を50℃にて0.5時間行った。続いてエチレングリコール10.0gをDMF50gと混合し添加後、60℃に昇温し、鎖長延長反応を行った。途中粘度上昇を見ながらDMF204gを分割添加しながら8時間反応させて、固形分中植物由来成分含有比率0.0%、オキシエチレン基含有比率が20.8%のポリウレタン樹脂30%溶液が得られた。
<Petroleum-derived moisture-permeable polyurethane resin 30% solution 2>
In a 1 L four-necked flask equipped with a stirrer and a thermometer, 60 g of polyethylene adipate (Nippon Polyurethane Co., Ltd., Nipponran N-4010) and 40 g of polyoxyethylene diol (Daiichi Kogyo Co., Ltd., D-300W) Then, 150 g of DMF was charged and dissolved uniformly. Under a temperature control of 50 ° C., 20.5 g of MDI was added and reacted for 1 hour, and then 42.5 g of MDI was added, and the prepolymer final reaction was performed at 50 ° C. for 0.5 hour. Subsequently, 10.0 g of ethylene glycol was mixed with 50 g of DMF and added, and then the temperature was raised to 60 ° C. to carry out a chain extension reaction. The reaction was carried out for 8 hours while adding 204 g of DMF while observing the increase in viscosity on the way, and a 30% polyurethane resin solution with a plant-derived component content ratio of solid content and a oxyethylene group content ratio of 20.8% was obtained. It was.

[実施例1]
上記〈植物由来ポリウレタン樹脂25%溶液1〉100重量部に、シリカ微粉末(富士シリシア化学工業(株)製、サイリシア350)3.5重量部を添加し、DMF25重量部で充分に浸漬し、ホモミキサーで約15分間分散攪拌後、フッ素系撥水剤(大日精化工業(株)製、ダイアロマーFF−121D)1重量部と顔料(大日本インキ化学工業(株)製、DILAC WHITE L 7551)2重量部、架橋剤(日本ポリウレタン(株)製、コロネートHL)1重量部を添加攪拌した、植物由来率24.5%(固形分中比率)のポリウレタン樹脂配合溶液を、タテヨコともに84デシテックスの糸よりなるポリエステル平織物を精錬、セット後、フッ素系撥水剤(ダイキン工業株式会社製、ユニダインTG−410)5重量%と水95重量%よりなる撥水液に絞り率約50%でパディング処理し、約120℃で乾燥後、片面を190℃で2回カレンダー処理した離型布のカレンダー面にナイフオーバーロール方式にて160g/mで塗布した。これをN,N−ジメチルホルムアミドの15重量%水溶液に浸漬し、凝固多孔膜化した後、N,N−ジメチルホルムアミドをほとんど残留しないように湯洗し、約120℃で乾燥して、透湿性と耐水性を併せもつ多孔質膜が離型布上に得られた。
[Example 1]
To 100 parts by weight of the above <plant-derived polyurethane resin 25% solution 1>, 3.5 parts by weight of silica fine powder (manufactured by Fuji Silysia Chemical Co., Ltd., Silicia 350) is added, and sufficiently immersed in 25 parts by weight of DMF, After dispersing and stirring with a homomixer for about 15 minutes, 1 part by weight of a fluorine-based water repellent (Dai-Ni Seika Kogyo Co., Ltd., Dialomer FF-121D) and a pigment (Dailac Ink Chemical Co., Ltd., DILAC WHITE L 7551) ) 2 parts by weight and 1 part by weight of a cross-linking agent (manufactured by Nippon Polyurethane Co., Ltd., Coronate HL) were added to and stirred for a polyurethane resin-containing solution with a plant-derived rate of 24.5% (solid content ratio). After refining and setting the polyester plain fabric made of yarn, 5% by weight of fluorine-based water repellent (Unikin TG-410, manufactured by Daikin Industries, Ltd.) and water 95 A pad of water repellent consisting of an amount of 50% is drawn at a drawing rate of about 50%, dried at about 120 ° C, and calendered on one side at 190 ° C twice. Application was at m 2 . This was immersed in a 15% by weight aqueous solution of N, N-dimethylformamide to form a coagulated porous film, washed with hot water so that almost no N, N-dimethylformamide remained, dried at about 120 ° C., and moisture permeable. And a porous membrane having both water resistance were obtained on the release cloth.

この離型布上の多孔質膜に、湿気硬化型ポリウレタン接着剤(大日本インキ化学工業(株)製、NH124)を100℃で熔融しながら、24メッシュのドットで点状にグラビアコーティングし、これに84デシテックスのポリエステル加工糸よりなる丸編天竺を積層し、48時間熟成後、離型布を剥離し、耐水圧が60kPa(ナイロン78デシテックスタフタを当てて測定)で透湿度は7,830g/m・24H(JIS1099 A−1)の透湿防水膜を積層した布帛が得られた。この布帛の透湿防水膜の植物由来比率は24.5%となる。 The porous film on the release cloth was gravure-coated with dots of 24 mesh while melting moisture-curing polyurethane adhesive (Dainippon Ink Chemical Co., Ltd., NH124) at 100 ° C. A round knitted sheet made of 84 dtex polyester yarn is laminated on this, and after aging for 48 hours, the release cloth is peeled off, the water pressure resistance is 60 kPa (measured by applying nylon 78 dtex sticker), and the moisture permeability is 7,830 g. A fabric laminated with a moisture permeable waterproof membrane of / m 2 · 24H (JIS 1099 A-1) was obtained. The plant-derived ratio of the moisture-permeable waterproof membrane of this fabric is 24.5%.

この透湿防水膜を積層した布帛の甲部の布帛面に反応性ホットメルト用ハンドガン(ドイツ・Reka社製、TR70.3)で湿気硬化型ポリウレタン接着剤(大日本インキ化学工業(株)製、NH124)を手の形に沿うように約2.5mmの幅に塗布し、この甲部と掌部とを貼り合せ、48時間熟成後、ほぼ指の形に沿う形状の手袋インサートが得られた。甲部と掌部とを張り合わせた接着部分が20kPaの耐水圧を有し、透湿防水膜の植物由来比率が24.5%である手袋インサートとなった。   Moisture curable polyurethane adhesive (manufactured by Dainippon Ink & Chemicals, Inc.) using a reactive hot-melt hand gun (manufactured by Reka, Germany, TR70.3) on the fabric surface of the upper part of the fabric laminated with this moisture permeable waterproof membrane , NH124) is applied to a width of about 2.5 mm so as to conform to the shape of the hand, and the upper part and the palm part are bonded together, and after aging for 48 hours, a glove insert having a shape substantially conforming to the shape of a finger is obtained. It was. The bonded part where the upper part and the palm part were pasted together had a water pressure resistance of 20 kPa, and the moisture-permeable waterproof membrane had a plant-derived ratio of 24.5%.

[実施例2]
上記〈植物由来ポリウレタン樹脂25%溶液2〉100重量部にシリカ微粉末(富士シリシア化学工業(株)製、サイリシア350)3.5重量部を添加、DMF25重量部で充分に浸漬、ホモミキサーで約15分間分散攪拌後、フッ素系撥水剤(大日精化工業(株)製、ダイアロマーFF−121D)1重量部と顔料(大日本インキ化学工業(株)製、DILAC WHITE L 7551)2重量部、架橋剤(日本ポリウレタン(株)製、コロネートHL)1重量部を添加攪拌した、植物由来率38.8%(固形分中比率)のポリウレタン樹脂配合溶液を、タテヨコともに84デシテックスの糸よりなるポリエステル平織物を精錬、セット後、フッ素系撥水剤(ダイキン工業株式会社製、ユニダインTG−410)5重量%と水95重量%よりなる撥水液に絞り率約50%でパディング処理し、約120℃で乾燥後、片面を190℃で2回カレンダー処理した離型布のカレンダー面にナイフオーバーロール方式にて160g/mで塗布した。これをN,N−ジメチルホルムアミドの15重量%水溶液に浸漬し、凝固多孔膜化した後、N,N−ジメチルホルムアミドをほとんど残留しないように湯洗し、約120℃で乾燥して、透湿性と耐水性を併せもつ多孔質膜が離型布上に得られた。
[Example 2]
Add <3.5 parts by weight of silica fine powder (manufactured by Fuji Silysia Chemical Co., Ltd., Silicia 350) to 100 parts by weight of the above <plant-derived polyurethane resin 25% solution 2>, and fully immerse in 25 parts by weight of DMF. After dispersing and stirring for about 15 minutes, 1 part by weight of a fluorine-based water repellent (Dai-Ni Seika Kogyo Co., Ltd., Dialomer FF-121D) and a pigment (Dailac Ink Chemical Co., Ltd., DILA WHITE L 7551) 2 wt. Part and a cross-linking agent (Nihon Polyurethane Co., Ltd., Coronate HL) 1 part by weight of a polyurethane resin-blended solution with a plant-derived rate of 38.8% (solid content ratio) from 84 decitex yarns for both vertical and horizontal After refining and setting the polyester plain fabric, 5% by weight of fluorine-based water repellent (Daikin Industries, Ltd., Unidyne TG-410) and 95% by weight of water Padding at about 50% throttle rate Li Cheng water repellent solution, dried at about 120 ° C., knife over roll system at 160 g / m 2 on the calendar surface of the calendered mold release cloth twice on one side at 190 ° C. It was applied with. This was immersed in a 15% by weight aqueous solution of N, N-dimethylformamide to form a coagulated porous film, washed with hot water so that almost no N, N-dimethylformamide remained, dried at about 120 ° C., and moisture permeable. And a porous membrane having both water resistance were obtained on the release cloth.

この離型布上の多孔質膜に、湿気硬化型ポリウレタン接着剤(大日本インキ化学工業(株)製、NH124)を100℃で熔融しながら、24メッシュのドットで点状にグラビアコーティングし、これに84デシテックスのポリエステル加工糸よりなる丸編天竺を積層し、48時間熟成後、離型布を剥離し、耐水圧が65kPa(ナイロン78デシテックスタフタを当てて測定)で透湿度は6,370g/m・24H(JIS1099 A−1)の透湿防水膜を積層した布帛が得られた。この布帛の透湿防水膜の植物由来比率は38.8%となる。 The porous film on the release cloth was gravure-coated with dots of 24 mesh while melting moisture-curing polyurethane adhesive (Dainippon Ink Chemical Co., Ltd., NH124) at 100 ° C. A round knitted sheet made of 84 dtex polyester yarn was laminated on this, and after aging for 48 hours, the release cloth was peeled off, the water pressure resistance was 65 kPa (measured by applying nylon 78 dtex sticker), and the moisture permeability was 6,370 g. A fabric laminated with a moisture permeable waterproof membrane of / m 2 · 24H (JIS 1099 A-1) was obtained. The plant-derived ratio of the moisture permeable waterproof membrane of this fabric is 38.8%.

この透湿防水膜を積層した布帛の甲部の布帛面に反応性ホットメルト用ハンドガン(ドイツ・Reka社製、TR70.3)で湿気硬化型ポリウレタン接着剤(大日本インキ化学工業(株)製、NH124)を手の形に沿うように、約2.5mmの幅に塗布し、この甲部と掌部とを貼り合せ、48時間熟成後、ほぼ指の形に沿う形状の手袋インサートインサートが得られた。甲部と掌部とを張り合わせた接着部分が20kPaの耐水圧を有する透湿防水膜の植物由来比率が38.8%の手袋インサートとなった。   Moisture curable polyurethane adhesive (manufactured by Dainippon Ink & Chemicals, Inc.) using a reactive hot-melt hand gun (manufactured by Reka, Germany, TR70.3) on the fabric surface of the upper part of the fabric laminated with this moisture permeable waterproof membrane , NH124) is applied to a width of about 2.5 mm so as to conform to the shape of the hand, the upper part and the palm part are bonded together, and after aging for 48 hours, a glove insert insert having a shape substantially conforming to the shape of a finger is obtained. Obtained. A glove insert having a plant-derived ratio of a moisture-permeable waterproof membrane having a water pressure resistance of 20 kPa at the bonded portion where the upper portion and the palm portion are bonded to each other is 38.8%.

[実施例3]
上記〈植物由来ポリウレタン樹脂25%溶液3〉100重量部にシリカ微粉末(富士シリシア化学工業(株)製、サイリシア350)3.5重量部を添加し、DMF25重量部で充分に浸漬し、ホモミキサーで約15分間分散攪拌後、フッ素系撥水剤(大日精化工業(株)製、ダイアロマーFF−121D)1重量部と顔料(大日本インキ化学工業(株)製、DILAC WHITE L 7551)2重量部、架橋剤(日本ポリウレタン(株)製、コロネートHL)1重量部を添加攪拌した、植物由来率48.1%(固形分中比率)のポリウレタン樹脂配合溶液を、タテヨコともに84デシテックスの糸よりなるポリエステル平織物を精錬、セット後、フッ素系撥水剤(ダイキン工業株式会社製、ユニダインTG−410)5重量%と水95重量%よりなる撥水液に絞り率約50%でパディング処理し、約120℃で乾燥後、片面を190℃で2回カレンダー処理した離型布のカレンダー面にナイフオーバーロール方式にて160g/mで塗布した。これをN,N−ジメチルホルムアミドの15重量%水溶液に浸清し、凝固多孔膜化した後、N,N−ジメチルホルムアミドをほとんど残留しないように湯洗し、約120℃で乾燥して、透湿性と耐水性を併せもつ多孔質膜が離型布上に得られた。
[Example 3]
3.5 parts by weight of silica fine powder (manufactured by Fuji Silysia Chemical Co., Ltd., Silicia 350) is added to 100 parts by weight of the <plant-derived polyurethane resin 25% solution 3> and sufficiently immersed in 25 parts by weight of DMF. After about 15 minutes of dispersion and stirring with a mixer, 1 part by weight of a fluorine-based water repellent (Dai-Ni Seika Kogyo Co., Ltd., Dialomer FF-121D) and a pigment (Dailac Ink Chemical Co., Ltd., DIRAC WHITE L 7551) 2 parts by weight and 1 part by weight of a cross-linking agent (manufactured by Nippon Polyurethane Co., Ltd., Coronate HL) were added and stirred. A plant-derived ratio of 48.1% (solid content ratio) polyurethane resin blended solution was 84 decitex for both vertical and horizontal After refining and setting polyester plain fabric made of yarn, fluorine water repellent (Daikin Industries, Unidyne TG-410) 5% by weight and water 95 times % From consisting padding at about 50% drawing rate water repellent solution, dried at about 120 ° C., 160 g / m with a knife over roll type calendar surface of the calendered mold release cloth twice on one side at 190 ° C. 2 was applied. This was immersed in a 15% by weight aqueous solution of N, N-dimethylformamide to form a coagulated porous film, then washed with hot water so that almost no N, N-dimethylformamide remained, dried at about 120 ° C., and permeable. A porous membrane having both wet and water resistance was obtained on the release cloth.

この離型布上の多孔質膜に、湿気硬化型ポリウレタン接着剤(大日本インキ化学工業(株)製、NH124)を100℃で熔融しながら、24メッシュのドットで点状にグラビアコーティングし、これに84デシテックスのポリエステル加工糸よりなる丸編天竺を積層し、48時間熟成後、離型布を剥離し、耐水圧が58kPa(ナイロン78デシテックスタフタを当てて測定)で透湿度は4,330g/m・24H(JIS1099 A−1)の透湿防水膜を積層した布帛が得られた。この布帛の透湿防水膜の植物由来比率は48.1%となる。 The porous film on the release cloth was gravure-coated with dots of 24 mesh while melting moisture-curing polyurethane adhesive (Dainippon Ink Chemical Co., Ltd., NH124) at 100 ° C. A round knitted sheet made of 84 dtex polyester yarn was laminated on this, and after aging for 48 hours, the release cloth was peeled off, the water pressure resistance was 58 kPa (measured by applying nylon 78 dtex sticker), and the moisture permeability was 4,330 g. A fabric laminated with a moisture permeable waterproof membrane of / m 2 · 24H (JIS 1099 A-1) was obtained. The plant-derived ratio of the moisture-permeable waterproof membrane of this fabric is 48.1%.

この透湿防水膜を積層した布帛の甲部の布帛面に反応性ホットメルト用ハンドガン(ドイツ・Reka社製、TR70.3)で湿気硬化型ポリウレタン接着剤(大日本インキ化学工業(株)製、NH124)を手の形に沿うように、約2.5mmの幅に塗布し、この甲部と掌部とを貼り合せ、48時間熟成後、ほぼ指の形に沿う形状の手袋インサートが得られた。甲部と掌部とを張り合わせた接着部分が20kPaの耐水圧を有する透湿防水膜の植物由来比率が48.1%の手袋インサートとなった。   Moisture curable polyurethane adhesive (manufactured by Dainippon Ink & Chemicals, Inc.) using a reactive hot-melt hand gun (manufactured by Reka, Germany, TR70.3) on the fabric surface of the upper part of the fabric laminated with this moisture permeable waterproof membrane , NH124) is applied to a width of about 2.5 mm so as to conform to the shape of the hand, and the upper part and the palm part are bonded together. After aging for 48 hours, a glove insert having a shape substantially conforming to the shape of a finger is obtained. It was. A glove insert having a plant-derived ratio of a moisture-permeable waterproof membrane having a water pressure resistance of 20 kPa at the bonded portion where the upper portion and the palm portion are bonded together is 48.1%.

[実施例4]
上記〈植物由来ポリウレタン樹脂25%溶液4〉100重量部にシリカ微粉末(富士シリシア化学工業(株)製、サイリシア350)3.5重量部を添加し、DMF25重量部で充分に浸漬し、ホモミキサーで約15分間分散攪拌後、フッ素系撥水剤(大日精化工業(株)製、ダイアロマーFF−121D)1重量部と顔料(大日本インキ化学工業(株)製、DILAC WHITE L 7551)2重量部、架橋剤(日本ポリウレタン(株)製、コロネートHL)1重量部を添加攪拌した、植物由来率51.7%(固形分中比率)のポリウレタン樹脂配合溶液を、タテヨコともに84デシテックスの糸よりなるポリエステル平織物を精錬、セット後、フッ素系撥水剤(ダイキン工業株式会社製、ユニダインTG−410)5重量%と水95重量%よりなる撥水液に絞り率約50%でパディング処理し、約120℃で乾燥後、片面を190℃で2回カレンダー処理した離型布のカレンダー面にナイフオーバーロール方式にて160g/mで塗布した。これをN,N−ジメチルホルムアミドの15重量%水溶液に浸清し、凝固多孔膜化した後、N,N−ジメチルホルムアミドをほとんど残留しないように湯洗し、約120℃で乾燥して、透湿性と耐水性を併せもつ多孔質膜が離型布上に得られた。
[Example 4]
3.5 parts by weight of silica fine powder (Fuji Silysia Chemical Co., Ltd., Silicia 350) is added to 100 parts by weight of the above <plant-derived polyurethane resin 25% solution 4>, and sufficiently immersed in 25 parts by weight of DMF. After dispersing and stirring with a mixer for about 15 minutes, 1 part by weight of a fluorine-based water repellent (Dai-Ni Seika Kogyo Co., Ltd., Dialomer FF-121D) and a pigment (Dailac Ink Chemical Co., Ltd., DILAC WHITE L 7551) 2 parts by weight and 1 part by weight of a cross-linking agent (manufactured by Nippon Polyurethane Co., Ltd., Coronate HL) were added and stirred. A polyurethane resin-containing solution with a plant-derived rate of 51.7% (solid content ratio) was 84 dtex for both vertical and horizontal. After refining and setting polyester plain fabric made of yarn, fluorine water repellent (Daikin Industries, Unidyne TG-410) 5% by weight and water 95 times % From consisting padding at about 50% drawing rate water repellent solution, dried at about 120 ° C., 160 g / m with a knife over roll type calendar surface of the calendered mold release cloth twice on one side at 190 ° C. 2 was applied. This was immersed in a 15% by weight aqueous solution of N, N-dimethylformamide to form a coagulated porous film, then washed with hot water so that almost no N, N-dimethylformamide remained, dried at about 120 ° C., and permeable. A porous membrane having both wet and water resistance was obtained on the release cloth.

この離型布上の多孔質膜に、湿気硬化型ポリウレタン接着剤(大日本インキ化学工業(株)製、NH124)を100℃で熔融しながら、24メッシュのドットで点状にグラビアコーティングし、これに84デシテックスのポリエステル加工糸よりなる丸編天竺を積層し、48時間熟成後、離型布を剥離し、耐水圧が32kPa(ナイロン78デシテックスタフタを当てて測定)で透湿度は2,830g/m・24H(JIS1099 A−1)の透湿防水膜を積層した布帛が得られた。この布帛の透湿防水膜の植物由来比率は48.1%となる。 The porous film on the release cloth was gravure-coated with dots of 24 mesh while melting moisture-curing polyurethane adhesive (Dainippon Ink Chemical Co., Ltd., NH124) at 100 ° C. A round knitted sheet made of 84 dtex polyester yarn was laminated on this, and after aging for 48 hours, the release cloth was peeled off, the water pressure resistance was 32 kPa (measured by applying nylon 78 dtex sticker), and the moisture permeability was 2,830 g. A fabric laminated with a moisture permeable waterproof membrane of / m 2 · 24H (JIS 1099 A-1) was obtained. The plant-derived ratio of the moisture-permeable waterproof membrane of this fabric is 48.1%.

この透湿防水膜を積層した布帛の甲部の布帛面に反応性ホットメルト用ハンドガン(ドイツ・Reka社製、TR70.3)で湿気硬化型ポリウレタン接着剤(大日本インキ化学工業(株)製、NH124)を手の形に沿うように、約2.5mmの幅に塗布し、この甲部と掌部とを貼り合せ、48時間熟成後、ほぼ指の形に沿う形状の手袋インサートが得られた。甲部と掌部とを張り合わせた接着部分が20kPaの耐水圧を有する透湿防水膜の植物由来比率が51.7%の手袋インサートとなった。   Moisture curable polyurethane adhesive (manufactured by Dainippon Ink & Chemicals, Inc.) using a reactive hot-melt hand gun (manufactured by Reka, Germany, TR70.3) on the fabric surface of the upper part of the fabric laminated with this moisture permeable waterproof membrane , NH124) is applied to a width of about 2.5 mm so as to conform to the shape of the hand, and the upper part and the palm part are bonded together. After aging for 48 hours, a glove insert having a shape substantially conforming to the shape of a finger is obtained. It was. A glove insert having a plant-derived ratio of a moisture-permeable waterproof membrane having a water pressure resistance of 20 kPa at the bonded portion where the upper portion and the palm portion are bonded together is 51.7%.

[実施例5]
上記〈植物由来透湿性ポリウレタン樹脂30%溶液1〉100重量部にMEK50重量部で希釈し調整した塗工液を、離型紙にコンマドクター方式にて75g/mで塗布し、約120℃で乾燥し、離型紙上に厚みが約15μmの無孔質の透湿性のポリウレタン防水膜が得られた。この膜に湿気硬化型ポリウレタン接着剤(大日本インキ化学工業(株)製、NH124)を100℃で熔融しながら、24メッシュのドットで点状にグラビアコーティングし、これに84デシテックスのポリエステル加工糸よりなる丸編天竺を積層し、48時間熟成後、離型布を剥離し、耐水圧が74kPa(ナイロン78デシテックスタフタを当てて測定)で透湿度は12,600g/m・24H(JIS1099 B−1)の透湿防水膜を積層した布帛が得られた。この布帛の透湿防水膜の植物由来比率は11.3%となる。
[Example 5]
<Plant-derived moisture-permeable polyurethane resin 30% solution 1> A coating solution diluted with 50 parts by weight of MEK and adjusted to 100 parts by weight is applied to a release paper at 75 g / m 2 by a comma doctor method at about 120 ° C. After drying, a nonporous moisture-permeable polyurethane waterproof membrane having a thickness of about 15 μm was obtained on the release paper. This film was coated with moisture-curing polyurethane adhesive (NH124, manufactured by Dainippon Ink & Chemicals, Inc.) at 100 ° C, and was gravure-coated with dots of 24 mesh. A circular knitted sheeting made up of the layers was laminated, and after aging for 48 hours, the release cloth was peeled off, the water pressure resistance was 74 kPa (measured by applying a nylon 78 decitech stuffer), and the moisture permeability was 12,600 g / m 2 · 24H (JIS 1099 B). A fabric in which the moisture permeable waterproof membrane of -1) was laminated was obtained. The plant-derived ratio of the moisture permeable waterproof membrane of this fabric is 11.3%.

この透湿防水膜を積層した布帛の甲部の布帛面に反応性ホットメルト用ハンドガン(ドイツ・Reka社製、TR70.3)で湿気硬化型ポリウレタン接着剤(大日本インキ化学工業(株)製、NH124)を手の形に沿うように、約2.5mmの幅に塗布し、この甲部と掌部とを貼り合せ、48時間熟成後、ほぼ指の形に沿う形状の手袋インサートが得られた。甲部と掌部とを張り合わせた接着部分が20kPaの耐水圧を有し、透湿防水膜の植物由来比率が11.3%の手袋インサートとなった。   Moisture curable polyurethane adhesive (manufactured by Dainippon Ink & Chemicals, Inc.) using a reactive hot-melt hand gun (manufactured by Reka, Germany, TR70.3) on the fabric surface of the upper part of the fabric laminated with this moisture permeable waterproof membrane , NH124) is applied to a width of about 2.5 mm so as to conform to the shape of the hand, and the upper part and the palm part are bonded together. After aging for 48 hours, a glove insert having a shape substantially conforming to the shape of a finger is obtained. It was. The bonded part where the upper part and the palm part were bonded together had a water pressure resistance of 20 kPa, and the moisture-permeable waterproof membrane was a glove insert having a plant-derived ratio of 11.3%.

[実施例6]
上記〈植物由来透湿性ポリウレタン樹脂30%溶液2〉100重量部にMEK50重量部で希釈し調整した塗工液を、離型紙にコンマドクター方式にて75g/mで塗布し、約120℃で乾燥し、離型紙上に厚みが約15μmの無孔質の透湿性のポリウレタン防水膜が得られた。この膜に湿気硬化型ポリウレタン接着剤(大日本インキ化学工業(株)製、NH124)を100℃で熔融しながら、24メッシュのドットで点状にグラビアコーティングし、これに84デシテックスのポリエステル加工糸よりなる丸編天竺を積層し、48時間熟成後、離型布を剥離し、耐水圧が104kPa(ナイロン78デシテックスタフタを当てて測定)で透湿度は9,400g/m・24H(JIS1099 B−1)の透湿防水膜を積層した布帛が得られた。この布帛の透湿防水膜の植物由来比率は28.4%となる。
[Example 6]
<Plant-derived moisture-permeable polyurethane resin 30% solution 2> A coating solution diluted with 50 parts by weight of MEK and adjusted to 100 parts by weight is applied to a release paper at 75 g / m 2 by a comma doctor method, and at about 120 ° C. After drying, a nonporous moisture-permeable polyurethane waterproof membrane having a thickness of about 15 μm was obtained on the release paper. This film was coated with moisture-curing polyurethane adhesive (NH124, manufactured by Dainippon Ink & Chemicals, Inc.) at 100 ° C, and was gravure-coated with dots of 24 mesh. A round knitted sheeting was laminated, and after aging for 48 hours, the release cloth was peeled off, the water pressure resistance was 104 kPa (measured by applying nylon 78 decitech stuffer), and the water vapor transmission rate was 9,400 g / m 2 · 24H (JIS 1099 B). A fabric in which the moisture permeable waterproof membrane of -1) was laminated was obtained. The plant-derived ratio of the moisture permeable waterproof membrane of this fabric is 28.4%.

この透湿防水膜を積層した布帛の甲部の布帛面に反応性ホットメルト用ハンドガン(ドイツ・Reka社製、TR70.3)で湿気硬化型ポリウレタン接着剤(大日本インキ化学工業(株)製、NH124)を手の形に沿うように、約2.5mmの幅に塗布し、この甲部と掌部とを貼り合せ、48時間熟成後、ほぼ指の形に沿う形状の手袋インサートが得られた。甲部と掌部とを張り合わせた接着部分が20kPaの耐水圧を有し、透湿防水膜の植物由来比率が28.4%の手袋インサートとなった。   Moisture curable polyurethane adhesive (manufactured by Dainippon Ink & Chemicals, Inc.) using a reactive hot-melt hand gun (manufactured by Reka, Germany, TR70.3) on the fabric surface of the upper part of the fabric laminated with this moisture permeable waterproof membrane , NH124) is applied to a width of about 2.5 mm so as to conform to the shape of the hand, and the upper part and the palm part are bonded together. After aging for 48 hours, a glove insert having a shape substantially conforming to the shape of a finger is obtained. It was. The adhesive part where the upper part and the palm part were bonded together had a water pressure resistance of 20 kPa, and the moisture-permeable waterproof membrane was a glove insert having a plant-derived ratio of 28.4%.

[実施例7]
上記〈植物由来透湿性ポリウレタン樹脂30%溶液3〉100重量部にMEK50重量部で希釈し調整した塗工液を、離型紙にコンマドクター方式にて75g/mで塗布し、約120℃で乾燥し、離型紙上に厚みが約15μmの無孔質の透湿性のポリウレタン防水膜が得られた。この膜に湿気硬化型ポリウレタン接着剤(大日本インキ化学工業(株)製、NH124)を100℃で熔融しながら、24メッシュのドットで点状にグラビアコーティングし、これに84デシテックスのポリエステル加工糸よりなる丸編天竺を積層し、48時間熟成後、離型布を剥離し、耐水圧が110kPa(ナイロン78デシテックスタフタを当てて測定)で透湿度は5,700g/m・24H(JIS1099 B−1)の透湿防水膜を積層した布帛が得られた。この布帛の透湿防水膜の植物由来比率は34.7%となる。
[Example 7]
<Plant-derived moisture-permeable polyurethane resin 30% solution 3> A coating solution diluted with 50 parts by weight of MEK and adjusted to 100 parts by weight is applied to a release paper at 75 g / m 2 by a comma doctor method at about 120 ° C. After drying, a nonporous moisture-permeable polyurethane waterproof membrane having a thickness of about 15 μm was obtained on the release paper. This film was coated with moisture-curing polyurethane adhesive (NH124, manufactured by Dainippon Ink & Chemicals, Inc.) at 100 ° C, and was gravure-coated with dots of 24 mesh. A circular knitted sheeting made up of 48 mm, and after aging for 48 hours, the release cloth was peeled off, the water pressure resistance was 110 kPa (measured by applying a nylon 78 decitech stuffer), and the moisture permeability was 5,700 g / m 2 · 24H (JIS 1099 B). A fabric in which the moisture permeable waterproof membrane of -1) was laminated was obtained. The plant-derived ratio of the moisture permeable waterproof membrane of this fabric is 34.7%.

この透湿防水膜を積層した布帛の甲部の布帛面に反応性ホットメルト用ハンドガン(ドイツ・Reka社製、TR70.3)で湿気硬化型ポリウレタン接着剤(大日本インキ化学工業(株)製、NH124)を手の形に沿うように、約2.5mmの幅に塗布し、掌部とを貼り合せ、48時間熟成後、ほぼ指の形に沿う形状の手袋インサートが得られた。この甲部と掌部とを張り合わせた接着部分が20kPaの耐水圧を有し、透湿防水膜の植物由来比率が34.7%の手袋インサートとなった。   Moisture curable polyurethane adhesive (manufactured by Dainippon Ink & Chemicals, Inc.) using a reactive hot-melt hand gun (manufactured by Reka, Germany, TR70.3) on the fabric surface of the upper part of the fabric laminated with this moisture permeable waterproof membrane , NH124) was applied to a width of about 2.5 mm so as to conform to the shape of the hand, and the palm part was bonded together. After aging for 48 hours, a glove insert having a shape substantially conforming to the shape of a finger was obtained. The bonded portion where the upper portion and the palm portion were bonded together had a water pressure resistance of 20 kPa, and the moisture-permeable waterproof membrane had a plant-derived ratio of 34.7%.

[実施例8]
上記〈植物由来透湿性ポリウレタン樹脂30%溶液4〉100重量部にMEK50重量部で希釈し調整した塗工液を、離型紙にコンマドクター方式にて75g/mで塗布し、約120℃で乾燥し、離型紙上に厚みが約15μmの無孔質の透湿性のポリウレタン防水膜ができる。この膜に湿気硬化型ポリウレタン接着剤(大日本インキ化学工業(株)製、NH124)を100℃で熔融しながら、24メッシュのドットで点状にグラビアコーティングし、これに84デシテックスのポリエステル加工糸よりなる丸編天竺を積層し、48時間熟成後、離型布を剥離し、耐水圧が134kPa(ナイロン78デシテックスタフタを当てて測定)で透湿度は3,100g/m・24H(JIS1099 B−1)の透湿防水膜を積層した布帛が得られた。この布帛の透湿防水膜の植物由来比率は39.6%となる。
[Example 8]
<Plant-derived moisture-permeable polyurethane resin 30% solution 4> A coating solution diluted with 50 parts by weight of MEK and adjusted to 100 parts by weight is applied to a release paper at 75 g / m 2 by a comma doctor method at about 120 ° C. After drying, a non-porous moisture-permeable polyurethane waterproof membrane having a thickness of about 15 μm can be formed on the release paper. This film was coated with moisture curing type polyurethane adhesive (Dainippon Ink Chemical Co., Ltd., NH124) at 100 ° C and gravure coated with dots of 24 mesh, and this was coated with 84 decitex polyester processed yarn. A circular knitted sheeting made of a laminate is laminated, and after aging for 48 hours, the release cloth is peeled off, the water pressure resistance is 134 kPa (measured by applying a nylon 78 decitech stuffer), and the moisture permeability is 3,100 g / m 2 · 24H (JIS 1099 B). A fabric in which the moisture-permeable waterproof membrane of -1) was laminated was obtained. The plant-derived ratio of the moisture-permeable waterproof membrane of this fabric is 39.6%.

この透湿防水膜を積層した布帛の甲部の布帛面に反応性ホットメルト用ハンドガン(ドイツ・Reka社製、TR70.3)で湿気硬化型ポリウレタン接着剤(大日本インキ化学工業(株)製、NH124)を手の形に沿うように、約2.5mmの幅に塗布し、この甲部と掌部とを貼り合せ、48時間熟成後、ほぼ指の形に沿う形状の手袋インサートが得られた。甲部と掌部とを張り合わせた接着部分が20kPaの耐水圧を有し、透湿防水膜の植物由来比率が39.6%の手袋インサートとなった。   Moisture curable polyurethane adhesive (manufactured by Dainippon Ink & Chemicals, Inc.) using a reactive hot-melt hand gun (manufactured by Reka, Germany, TR70.3) on the fabric surface of the upper part of the fabric laminated with this moisture permeable waterproof membrane , NH124) is applied to a width of about 2.5 mm so as to conform to the shape of the hand, and the upper part and the palm part are bonded together. After aging for 48 hours, a glove insert having a shape substantially conforming to the shape of a finger is obtained. It was. The adhesive part where the upper part and the palm part were bonded together had a water pressure resistance of 20 kPa, and the moisture-permeable waterproof membrane was a glove insert having a plant-derived ratio of 39.6%.

[実施例9]
上記〈植物由来透湿性ポリウレタン樹脂30%溶液5〉100重量部にMEK:50重量部で希釈し調整した塗工液を、離型紙にコンマドクター方式にて75g/mで塗布し、約120℃で乾燥し、離型紙上に厚みが約15μmの無孔質の透湿性のポリウレタン防水膜が得られた。この膜に湿気硬化型ポリウレタン接着剤(大日本インキ化学工業(株)製、NH124)を100℃で熔融しながら、24メッシュのドットで点状にグラビアコーティングし、これに84デシテックスのポリエステル加工糸よりなる丸編天竺を積層し、48時間熟成後、離型布を剥離し、耐水圧が152kPa(ナイロン78デシテックスタフタを当てて測定)で透湿度は2,400g/m・24H(JIS1099 B−1)の透湿防水膜を積層した布帛が得られた。この布帛の透湿防水膜の植物由来比率は46.3%となる。
[Example 9]
The above-mentioned <plant-derived moisture-permeable polyurethane resin 30% solution 5> The coating liquid diluted with 50 parts by weight of MEK and adjusted to 100 parts by weight is applied to a release paper at 75 g / m 2 by a comma doctor method, and about 120 It was dried at 0 ° C. to obtain a nonporous moisture-permeable polyurethane waterproof membrane having a thickness of about 15 μm on the release paper. This film was coated with moisture-curing polyurethane adhesive (NH124, manufactured by Dainippon Ink & Chemicals, Inc.) at 100 ° C, and was gravure-coated with dots of 24 mesh. A circular knitted sheeting made of a laminate is laminated, and after aging for 48 hours, the release cloth is peeled off, the water pressure resistance is 152 kPa (measured by applying a nylon 78 decitech stuffer), and the moisture permeability is 2,400 g / m 2 · 24H (JIS 1099 B). A fabric in which the moisture permeable waterproof membrane of -1) was laminated was obtained. The plant-derived ratio of the moisture-permeable waterproof membrane of this fabric is 46.3%.

この透湿防水膜を積層した布帛の甲部の布帛面に反応性ホットメルト用ハンドガン(ドイツ・Reka社製、TR70.3)で湿気硬化型ポリウレタン接着剤(大日本インキ化学工業(株)製、NH124)を手の形に沿うように、約2.5mmの幅に塗布し、掌部とを貼り合せ、48時間熟成後、ほぼ指の形に沿う形状の手袋インサートが得られた。甲部と掌部とを張り合わせた接着部分が20kPaの耐水圧を有し、透湿防水膜の植物由来比率が46.3%の手袋インサートとなった。   Moisture curable polyurethane adhesive (manufactured by Dainippon Ink & Chemicals, Inc.) using a reactive hot-melt hand gun (manufactured by Reka, Germany, TR70.3) on the fabric surface of the upper part of the fabric laminated with this moisture permeable waterproof membrane , NH124) was applied to a width of about 2.5 mm so as to conform to the shape of the hand, and the palm part was bonded together. After aging for 48 hours, a glove insert having a shape substantially conforming to the shape of a finger was obtained. The bonded portion where the upper portion and the palm portion were bonded together had a water pressure resistance of 20 kPa, and the moisture-permeable waterproof membrane was a glove insert having a plant-derived ratio of 46.3%.

[比較例1]
上記〈石油由来ポリウレタン樹脂25%溶液1〉100重量部にシリカ微粉末(富士シリシア化学工業(株)製、サイリシア350)3.5重量部を添加、DMF25重量部で充分に浸漬、ホモミキサーで約15分間分散攪拌後、フッ素系撥水剤(大日精化工業(株)製、ダイアロマーFF−121D)1重量部と顔料(大日本インキ化学工業(株)製、DILAC WHITE L 7551)2重量部、架橋剤(日本ポリウレタン(株)製、コロネートHL)1重量部を添加攪拌した、植物由来率0.0%(固形分中比率)のポリウレタン樹脂配合溶液を、タテヨコともに84デシテックスの糸よりなるポリエステル平織物を精錬、セット後、フッ素系撥水剤(ダイキン工業株式会社製、ユニダインTG−410)5重量%と水95重量%よりなる撥水液に絞り率約50%でパディング処理し、約120℃で乾燥後、片面を190℃で2回カレンダー処理した離型布のカレンダー面にナイフオーバーロール方式にて160g/mで塗布した。これをN,N−ジメチルホルムアミドの15重量%水溶液に浸漬し、凝固多孔膜化した後、N,N−ジメチルホルムアミドをほとんど残留しないように湯洗し、約120℃で乾燥して、透湿性と耐水性を併せもつ多孔質膜が離型布上に得られた。
[Comparative Example 1]
<Petroleum-derived polyurethane resin 25% solution 1> Add 100 parts by weight of silica fine powder (Fuji Silysia Chemical Co., Ltd., Silicia 350) 3.5 parts by weight, fully immersed in 25 parts by weight of DMF, and homomixer After dispersing and stirring for about 15 minutes, 1 part by weight of a fluorine-based water repellent (Dai-Ni Seika Kogyo Co., Ltd., Dialomer FF-121D) and a pigment (Dailac Ink Chemical Co., Ltd., DILA WHITE L 7551) 2 wt. Part and a crosslinking agent (manufactured by Nippon Polyurethane Co., Ltd., Coronate HL) 1 part by weight of a polyurethane resin compounded solution with a plant-derived rate of 0.0% (solid content ratio) from both 84 decitex yarns After refining and setting the polyester plain fabric, 5% by weight of fluorine-based water repellent (Daikin Industries, Ltd., Unidyne TG-410) and 95% by weight of water Comprising padding at about 50% drawing rate water repellent solution, dried at about 120 ° C., the calendar face twice calendering the release fabric on one side at 190 ° C. with a knife-over-roll method with 160 g / m 2 Applied. This was immersed in a 15% by weight aqueous solution of N, N-dimethylformamide to form a coagulated porous film, washed with hot water so that almost no N, N-dimethylformamide remained, dried at about 120 ° C., and moisture permeable. And a porous membrane having both water resistance were obtained on the release cloth.

この離型布上の多孔質膜に、湿気硬化型ポリウレタン接着剤(大日本インキ化学工業(株)製、NH124)を100℃で熔融しながら、24メッシュのドットで点状にグラビアコーティングし、これに84デシテックスのポリエステル加工糸よりなる丸編天竺を積層し、48時間熟成後、離型布を剥離し、耐水圧が62kPa(ナイロン78デシテックスタフタを当てて測定)で透湿度は8,120g/m・24H(JIS1099 A−1)の透湿防水膜を積層した布帛が得られた。この布帛の透湿防水膜の植物由来比率は0.0%となる。 The porous film on the release cloth was gravure-coated with dots of 24 mesh while melting moisture-curing polyurethane adhesive (Dainippon Ink Chemical Co., Ltd., NH124) at 100 ° C. A round knitted sheet made of 84 dtex polyester yarn was laminated on this, and after aging for 48 hours, the release cloth was peeled off, the water pressure resistance was 62 kPa (measured with a nylon 78 dtex stamper), and the moisture permeability was 8,120 g. A fabric laminated with a moisture permeable waterproof membrane of / m 2 · 24H (JIS 1099 A-1) was obtained. The plant-derived ratio of the moisture-permeable waterproof membrane of this fabric is 0.0%.

この透湿防水膜を積層した布帛の甲部の布帛面に反応性ホットメルト用ハンドガン(ドイツ・Reka社製、TR70.3)で湿気硬化型ポリウレタン接着剤(大日本インキ化学工業(株)製、NH124)を手の形に沿うように、約2.5mmの幅に塗布し、この甲部と掌部とを貼り合せ、48時間熟成後、ほぼ指の形に沿う形状の手袋インサートが得られた。甲部と掌部とを張り合わせた接着部分が20kPaの耐水圧を有し、透湿防水膜の植物由来比率が0.0%の手袋インサートとなった。   Moisture curable polyurethane adhesive (manufactured by Dainippon Ink & Chemicals, Inc.) using a reactive hot-melt hand gun (manufactured by Reka, Germany, TR70.3) on the fabric surface of the upper part of the fabric laminated with this moisture permeable waterproof membrane , NH124) is applied to a width of about 2.5 mm so as to conform to the shape of the hand, and the upper part and the palm part are bonded together. After aging for 48 hours, a glove insert having a shape substantially conforming to the shape of a finger is obtained. It was. The bonded part where the upper part and the palm part were bonded together had a water pressure resistance of 20 kPa, and the moisture-permeable waterproof membrane was a glove insert having a plant-derived ratio of 0.0%.

[比較例2]
上記〈石油由来透湿性ポリウレタン樹脂30%溶液2〉100重量部にMEK:50重量部で希釈し調整した塗工液を、離型紙にコンマドクター方式にて75g/mで塗布し、約120℃で乾燥し、離型紙上に厚みが約15μmの無孔質の透湿性のポリウレタン防水膜が得られた。この膜に湿気硬化型ポリウレタン接着剤(大日本インキ化学工業(株)製、NH124)を100℃で熔融しながら、24メッシュのドットで点状にグラビアコーティングし、これに84デシテックスのポリエステル加工糸よりなる丸編天竺を積層し、48時間熟成後、離型布を剥離し、耐水圧が128kPa(ナイロン78デシテックスタフタを当てて測定)で透湿度は5,100g/m・24H(JIS1099 B−1)の透湿防水膜を積層した布帛が得られた。この布帛の透湿防水膜の植物由来比率は0.0%となる。
[Comparative Example 2]
<Petroleum-derived moisture-permeable polyurethane resin 30% solution 2> A coating solution diluted with 50 parts by weight of MEK and adjusted to 100 parts by weight is applied to a release paper at 75 g / m 2 by a comma doctor method, and about 120 It was dried at 0 ° C. to obtain a nonporous moisture-permeable polyurethane waterproof membrane having a thickness of about 15 μm on the release paper. This film was coated with moisture-curing polyurethane adhesive (NH124, manufactured by Dainippon Ink & Chemicals, Inc.) at 100 ° C, and was gravure-coated with dots of 24 mesh. A circular knitted sheeting made of a laminate is laminated, and after aging for 48 hours, the release cloth is peeled off, the water pressure resistance is 128 kPa (measured by applying nylon 78 decitech stuffer), and the moisture permeability is 5,100 g / m 2 · 24H (JIS 1099 B). A fabric in which the moisture permeable waterproof membrane of -1) was laminated was obtained. The plant-derived ratio of the moisture-permeable waterproof membrane of this fabric is 0.0%.

この透湿防水膜を積層した布帛の甲部の布帛面に反応性ホットメルト用ハンドガン(ドイツ・Reka社製、TR70.3)で湿気硬化型ポリウレタン接着剤(大日本インキ化学工業(株)製、NH124)を手の形に沿うように、約2.5mmの幅に塗布し、この甲部と掌部とを貼り合せ、48時間熟成後、ほぼ指の形に沿う形状の手袋インサートが得られた。甲部と掌部とを張り合わせた接着部分が20kPaの耐水圧を有し、透湿防水膜の植物由来比率が0.0%の手袋インサートとなった。   Moisture curable polyurethane adhesive (manufactured by Dainippon Ink & Chemicals, Inc.) using a reactive hot-melt hand gun (manufactured by Reka, Germany, TR70.3) on the fabric surface of the upper part of the fabric laminated with this moisture permeable waterproof membrane , NH124) is applied to a width of about 2.5 mm so as to conform to the shape of the hand, and the upper part and the palm part are bonded together. After aging for 48 hours, a glove insert having a shape substantially conforming to the shape of a finger is obtained. It was. The bonded part where the upper part and the palm part were bonded together had a water pressure resistance of 20 kPa, and the moisture-permeable waterproof membrane was a glove insert having a plant-derived ratio of 0.0%.

Figure 2009161898
Figure 2009161898

Figure 2009161898
Figure 2009161898

本発明の手袋インサートは、一般スポーツ用および特にスキー、登山、ライディング、ハンティング用途に好適に用いられる。   The glove insert of the present invention is suitably used for general sports and especially for skiing, mountain climbing, riding and hunting.

Claims (9)

甲部と掌部とがそれぞれ透湿防水膜と布帛との積層体からなり、前記布帛側の面の周縁部において接着剤によって張り合わされて、ほぼ指の形に沿う形状に形成された手袋インサートであって、
前記透湿防水膜が植物由来成分を10〜80重量%含有するポリウレタン樹脂膜からなることを特徴とする手袋インサート。
A glove insert in which the upper part and the palm part are each composed of a laminate of a moisture permeable waterproof membrane and a cloth, and are bonded to each other at the peripheral part of the cloth side surface by an adhesive so as to substantially conform to the shape of a finger. Because
The glove insert characterized in that the moisture-permeable waterproof membrane is made of a polyurethane resin membrane containing 10 to 80% by weight of plant-derived components.
前記ポリウレタン樹脂を構成するポリオール成分としてヒマシ油ジオールを用いたことを特徴とする、請求項1に記載の手袋インサート。   2. The glove insert according to claim 1, wherein a castor oil diol is used as a polyol component constituting the polyurethane resin. 前記ヒマシ油ジオールがヒマシ油系ポリエーテルポリエステルジオールであって、平均水酸基数が1.8〜2.1個であり、水酸基価が41〜85mgKOH/gであることを特徴とする、請求項2に記載の手袋インサート。   The castor oil diol is a castor oil-based polyether polyester diol having an average number of hydroxyl groups of 1.8 to 2.1 and a hydroxyl value of 41 to 85 mgKOH / g. Glove insert as described in 前記植物由来成分を10〜80重量%含有するポリウレタン樹脂膜が湿式膜成形技法により形成された多孔膜であって、透湿防水膜を積層した布帛の耐水圧が10kPa以上であり、透湿度がJIS 1099 A−1法で2,000g/m・24H以上であることを特徴とする、請求項1〜3のいずれか1項に記載の手袋インサート。 The polyurethane resin film containing 10 to 80% by weight of the plant-derived component is a porous film formed by a wet film forming technique, the water pressure resistance of the fabric laminated with the moisture permeable waterproof film is 10 kPa or more, and the moisture permeability is The glove insert according to any one of claims 1 to 3, wherein the glove insert is 2,000 g / m 2 · 24H or more according to JIS 1099 A-1. 前記植物由来成分を10〜80重量%含有するポリウレタン樹脂膜が乾式膜成形技法により形成された無孔膜であって、透湿防水膜を積層した布帛の耐水圧が10kPa以上であり、透湿度がJIS 1099 B−1法で2,000g/m・24H以上であることを特徴とする、請求項1〜3のいずれか1項に記載の手袋インサート。 A polyurethane resin film containing 10 to 80% by weight of the plant-derived component is a non-porous film formed by a dry film forming technique, and the water pressure resistance of a fabric laminated with a moisture permeable waterproof film is 10 kPa or more, The glove insert according to any one of claims 1 to 3, wherein JIS 1099 B-1 method is 2,000 g / m 2 · 24H or more. 植物由来成分の含有量が25〜65重量%であることを特徴とする、請求項1〜5のいずれか1項に記載の手袋インサート。   The glove insert according to any one of claims 1 to 5, wherein the content of the plant-derived component is 25 to 65% by weight. 前記甲部と掌部とが接着剤によって張り合わされた接着部の巾が1〜5mmであることを特徴とする、請求項1〜6のいずれか1項に記載の手袋インサート。   The glove insert according to any one of claims 1 to 6, wherein a width of an adhesive part in which the upper part and the palm part are bonded together by an adhesive is 1 to 5 mm. 前記甲部と掌部とを張り合わせた接着部分が10kPa以上の耐水圧を有することを特徴とする、請求項1〜7のいずれか1項に記載の手袋インサート。   The glove insert according to any one of claims 1 to 7, wherein a bonded portion obtained by bonding the upper portion and the palm portion has a water pressure resistance of 10 kPa or more. 前記布帛がタテ又はヨコのいずれかにおいて100%以上の伸度を有することを特徴とする、請求項1〜8のいずれか1項に記載の手袋インサート。   The glove insert according to any one of claims 1 to 8, wherein the fabric has an elongation of 100% or more in either length or width.
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Cited By (4)

* Cited by examiner, † Cited by third party
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WO2011105595A1 (en) * 2010-02-23 2011-09-01 セーレン株式会社 Moisture-permeable water-proofing cloth
WO2021054130A1 (en) * 2019-09-20 2021-03-25 Dic株式会社 Moisture-permeable waterproof fabric
WO2021132657A1 (en) * 2019-12-26 2021-07-01 東レコーテックス株式会社 Moisture-permeable waterproof fabric
JPWO2020262182A1 (en) * 2019-06-25 2021-09-13 Dic株式会社 Moisture-curable polyurethane resin composition, adhesive, and laminate

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2011105595A1 (en) * 2010-02-23 2011-09-01 セーレン株式会社 Moisture-permeable water-proofing cloth
CN102762792A (en) * 2010-02-23 2012-10-31 世联株式会社 Moisture-permeable water-proofing cloth
CN102762792B (en) * 2010-02-23 2014-06-25 世联株式会社 Moisture-permeable water-proofing cloth
JPWO2020262182A1 (en) * 2019-06-25 2021-09-13 Dic株式会社 Moisture-curable polyurethane resin composition, adhesive, and laminate
WO2021054130A1 (en) * 2019-09-20 2021-03-25 Dic株式会社 Moisture-permeable waterproof fabric
JPWO2021054130A1 (en) * 2019-09-20 2021-11-25 Dic株式会社 Breathable waterproof fabric
CN114258442A (en) * 2019-09-20 2022-03-29 Dic株式会社 Moisture-permeable waterproof fabric
CN114258442B (en) * 2019-09-20 2023-09-15 Dic株式会社 Moisture-permeable waterproof fabric
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