JPS607876A - Artificial leather glove for golf - Google Patents
Artificial leather glove for golfInfo
- Publication number
- JPS607876A JPS607876A JP58114303A JP11430383A JPS607876A JP S607876 A JPS607876 A JP S607876A JP 58114303 A JP58114303 A JP 58114303A JP 11430383 A JP11430383 A JP 11430383A JP S607876 A JPS607876 A JP S607876A
- Authority
- JP
- Japan
- Prior art keywords
- fibers
- fiber
- ultrafine
- layer
- artificial leather
- 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.)
- Granted
Links
- 239000002649 leather substitute Substances 0.000 title claims description 20
- 239000000835 fiber Substances 0.000 claims description 90
- 229920001410 Microfiber Polymers 0.000 claims description 36
- 229920005989 resin Polymers 0.000 claims description 30
- 239000011347 resin Substances 0.000 claims description 30
- 239000000463 material Substances 0.000 claims description 9
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims description 7
- 229910052709 silver Inorganic materials 0.000 claims description 7
- 239000004332 silver Substances 0.000 claims description 7
- 239000002131 composite material Substances 0.000 claims description 2
- 238000009958 sewing Methods 0.000 claims description 2
- 239000003658 microfiber Substances 0.000 claims 1
- 239000010410 layer Substances 0.000 description 39
- -1 polyethylene terephthalate Polymers 0.000 description 16
- 229920002635 polyurethane Polymers 0.000 description 12
- 239000004814 polyurethane Substances 0.000 description 12
- 238000000034 method Methods 0.000 description 11
- 239000012530 fluid Substances 0.000 description 9
- 239000004745 nonwoven fabric Substances 0.000 description 8
- 238000011282 treatment Methods 0.000 description 8
- 239000000243 solution Substances 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
- 238000009987 spinning Methods 0.000 description 6
- 239000004793 Polystyrene Substances 0.000 description 4
- 239000000470 constituent Substances 0.000 description 4
- 229920000139 polyethylene terephthalate Polymers 0.000 description 4
- 239000005020 polyethylene terephthalate Substances 0.000 description 4
- 229920002223 polystyrene Polymers 0.000 description 4
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 239000004952 Polyamide Substances 0.000 description 3
- 239000002202 Polyethylene glycol Substances 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 229920002647 polyamide Polymers 0.000 description 3
- 229920001223 polyethylene glycol Polymers 0.000 description 3
- 238000004080 punching Methods 0.000 description 3
- 239000002344 surface layer Substances 0.000 description 3
- 235000017166 Bambusa arundinacea Nutrition 0.000 description 2
- 235000017491 Bambusa tulda Nutrition 0.000 description 2
- 241001330002 Bambuseae Species 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
- 229920002292 Nylon 6 Polymers 0.000 description 2
- 235000015334 Phyllostachys viridis Nutrition 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 239000011425 bamboo Substances 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 238000004049 embossing Methods 0.000 description 2
- 239000010985 leather Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 229920002285 poly(styrene-co-acrylonitrile) Polymers 0.000 description 2
- 229920001707 polybutylene terephthalate Polymers 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 229920005749 polyurethane resin Polymers 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 238000010008 shearing Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 210000004243 sweat Anatomy 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- WCVOGSZTONGSQY-UHFFFAOYSA-N 2,4,6-trichloroanisole Chemical compound COC1=C(Cl)C=C(Cl)C=C1Cl WCVOGSZTONGSQY-UHFFFAOYSA-N 0.000 description 1
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 1
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 229920000299 Nylon 12 Polymers 0.000 description 1
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- 229920002522 Wood fibre Polymers 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000003491 array Methods 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 239000000986 disperse dye Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000009499 grossing Methods 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- 239000011229 interlayer Substances 0.000 description 1
- 238000009981 jet dyeing Methods 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229920003145 methacrylic acid copolymer Polymers 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229920005615 natural polymer Polymers 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920000921 polyethylene adipate Polymers 0.000 description 1
- 239000002952 polymeric resin Substances 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920006264 polyurethane film Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 238000007763 reverse roll coating Methods 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 238000010345 tape casting Methods 0.000 description 1
- 238000009423 ventilation Methods 0.000 description 1
- 239000002025 wood fiber Substances 0.000 description 1
- 230000037303 wrinkles Effects 0.000 description 1
Landscapes
- Gloves (AREA)
- Synthetic Leather, Interior Materials Or Flexible Sheet Materials (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Abstract] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
本発明はゴルフ用人工皮革手袋に関する。さらに詳しく
はゴルフクラブのグリップとフィツト性が良い人工皮革
ゴルフ用手袋に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an artificial leather golf glove. More specifically, the present invention relates to artificial leather golf gloves that have good golf club grip and fit.
従来ゴルフ用手袋として−、天然皮革が主と1−で用い
られてきたが、グリップとフィツト性の良いものは、す
ぐに破れるとか、グリップとの摩擦や手の汗によって真
っ黒に汚れ、しかも洗たくができないというような機能
性の点が劣り、より良いゴルフ手袋用素材がめられてき
た。これに対し近年人工皮革のスェード調タイプがゴル
フ手袋として用いられ、確力・に破れにくくなるとか、
水洗いができるとかの機能性が向上してきた。しかし肝
心のゴルフクラブのグリップ(ゴム製、皮製を問わない
)とのフィツト性という点でニ、渭りやすく未だ劣って
いるため、さらにより良い累月がめられている。Conventionally, natural leather has been mainly used as golf gloves, but the ones with good grip and fit tend to tear easily, become black due to friction with the grip and sweat from the hands, and are difficult to wash. Due to the lack of functionality, such as the inability to wear gloves, better materials for golf gloves have been sought. In contrast, in recent years, suede-like types of artificial leather have been used as golf gloves, and are said to be more durable and less likely to tear.
Its functionality has improved, such as the ability to wash it with water. However, in terms of the essential fit with the grip of a golf club (regardless of whether it is made of rubber or leather), it is still inferior in that it tends to become loose, so there is a need for an even better grip.
本発明の目的はかかるグリップとのフィン1、性に優れ
た人工皮革ゴルフ手袋を提供するものである。しかも外
観品位、柔らかさとしなやかさに優れた人工皮革ゴルフ
手袋を提供するものである。The object of the present invention is to provide an artificial leather golf glove having such a grip and fins 1 and excellent properties. Moreover, the present invention provides artificial leather golf gloves that are excellent in appearance quality, softness, and suppleness.
すなわち本発明の人工皮革ゴルフ手袋に一1極細繊維束
から枝分れした極細繊維およ改またはその束が緻密に交
絡し、その空隙に樹脂が存在しているような繊維質銀面
層が、ゴルフグラブのグリップと接触するため、従来の
ポリウレタン膜の銀面層をもつ銀材人工皮革とか、極細
繊維立毛層をもつスェード調人工皮革とは全く異なった
フイ・ット性、特にグリップに吸いつくようなフィツト
性を示すのである。しかも繊維自身は銀面層と内部で連
続しているため、銀面がはがれるとか、せん断で破れを
生じるとかの耐久性も良好であr、tた人工皮革のため
洗たくも可能であり、優れたゴルフ手袋となるのである
。That is, the artificial leather golf glove of the present invention has a fibrous grain layer in which ultrafine fibers branched from an ultrafine fiber bundle or bundles thereof are densely intertwined and resin is present in the voids. Because it comes into contact with the grip of a golf glove, it has a completely different fit and fit, especially in grips, than conventional silver artificial leather with a silver surface layer of polyurethane film or suede-like artificial leather with a napped layer of ultra-fine fibers. It exhibits a snug fit. Moreover, since the fiber itself is continuous with the grain layer inside, it has good durability against peeling of the grain surface or tearing due to shearing, and because it is made of artificial leather, it can be easily washed. It becomes a golf glove.
下
本発明に使用される0、05デニ一ル以上の極細繊維は
、つぎに述べる極細繊維形成型繊維を用い加工工程中の
適当な時期に極細繊維に変成して用いることが好ましい
。すなわち2本発明に使用される極細繊維形成型繊維は
、たとえば、紡糸直後で極細繊維を集束し部分的に軽く
接着して1本にした繊維、1成分を他成分間に放射状に
介在せしめた菊花状断面の繊維、多層バイメタル型繊維
。The ultrafine fibers of 0.05 denier or more used in the present invention are preferably used after being modified into ultrafine fibers at an appropriate time during the processing process using ultrafine fiber-forming fibers described below. In other words, the ultrafine fiber-forming fiber used in the present invention is, for example, a fiber made by gathering ultrafine fibers immediately after spinning and lightly adhering them into a single fiber, or a fiber in which one component is radially interposed between other components. Chrysanthemum-shaped cross-section fiber, multilayer bimetallic fiber.
ドーナツ状断面の多層バイメタル型繊維、2成分以上の
成分を溶融混合して紡糸した海島繊維、繊維軸方向に連
続した極細繊維が多数配列集合し他の成分で結合および
/または一部結合され1木の繊維を形成した高分子相互
配列体繊維などであり。Multilayer bimetallic fiber with a doughnut-shaped cross section, sea-island fiber made by melt-mixing and spinning two or more components, and a large number of ultrafine fibers continuous in the fiber axis direction, which are arranged and aggregated and bonded and/or partially bonded with other components. Wood fibers are formed by polymeric interlayer arrays such as fibers.
これらの2種以上の繊維を混合あるいは組み合せて用い
てもよい。複数の芯が他成分により介在的に結合および
/または一部結合された横断面を有する極細繊維形成型
繊維は物理的作用を加えるあるいは結合成分の除去など
によシ比較的容易に極細繊維が得られるため奸才しく用
いられる。また少なくとも1成分を溶解除去したとき好
ましくは0.05デニール以下、更に好ましくはo、
o o i以下の極細繊維を主体とする繊維の束が得ら
れる多成分からなる極細繊維形成型繊維は、特にしなや
かな風合、なめらかな表面を有する皮革様シート物が得
られるため、さらに好ましく用いられる。Two or more types of these fibers may be mixed or used in combination. Ultrafine fiber-forming fibers having a cross section in which a plurality of cores are interveningly bonded and/or partially bonded by other components can be relatively easily formed into ultrafine fibers by applying physical action or removing bonded components. It is used cleverly because it can be obtained. Further, when at least one component is dissolved and removed, preferably 0.05 denier or less, more preferably o,
Multi-component ultrafine fiber-forming fibers that yield bundles of fibers mainly consisting of ultrafine fibers of o o i or less are more preferred because they yield a leather-like sheet material with a particularly supple texture and smooth surface. used.
また1本発明における極細繊維は繊維形成能を有する高
分子物質からなシ1例えば、ナーイロン6゜ナイロン6
6、ナイロン12.共重合ナイロンなどのポリアミド、
ポリエチレンテレフタレート。Further, the ultrafine fibers in the present invention are made of a polymeric substance having fiber-forming ability.1 For example, nylon 6° nylon 6
6. Nylon 12. Polyamides such as copolymerized nylon,
polyethylene terephthalate.
共重合ポリエチレンテレフタレート、ポリブチレンテレ
フタレート、共重合ポリブチレンテレフタレートなどの
ポリエステル、ポリエチレン、ポリプロピレンなどのポ
リオレフィン、ポリウレタン。Polyesters such as copolymerized polyethylene terephthalate, polybutylene terephthalate, and copolymerized polybutylene terephthalate, polyolefins such as polyethylene and polypropylene, and polyurethane.
ポリアクリロニトリルおよびビニル重合体などがあげら
れる。また、該極細繊維形成型繊維の結合成分あるいは
溶解除去成分としては1例えば、ポリスチレン、ポリエ
チレン、ポリプロピレン、ポリアミド、ポリウレタン、
アルカリ溶液に易溶出型の共重合ポリエチレンテレフタ
レート、共重合ポリビニルアルコール、共重合ポリビニ
ルアルコール、スチレン−アクリロニトリル共重合体、
スチレンとアクリル酸の高級アルコールエステルおよび
/またはメタクリル酸の高級アルコールエステルとの共
重合体などが用いられる。紡糸のしやすさ、溶解除去の
容易さの点でポリスチレン、スチレン−アクリロニトリ
ル共重合体、スチレンとアクリル酸の高級アルコールエ
ステルおよび/またけメタクリル酸の高級アルコールエ
ステルとの共重合体は好ましく用いられる。さらに延伸
倍率が高くとれ強度の高い繊維が得られるという点でA
チレンとアクリル酸の高級アルコールエステルおよび/
またはメタクリル酸の高級アルコールエステルとの共重
合体はさらに好ましく用いられる。Examples include polyacrylonitrile and vinyl polymers. In addition, examples of the binding component or the dissolving and removing component of the microfiber-forming fiber include polystyrene, polyethylene, polypropylene, polyamide, polyurethane,
Copolymerized polyethylene terephthalate, copolymerized polyvinyl alcohol, copolymerized polyvinyl alcohol, styrene-acrylonitrile copolymer, easily soluble in alkaline solutions,
A copolymer of styrene and a higher alcohol ester of acrylic acid and/or a higher alcohol ester of methacrylic acid is used. Polystyrene, styrene-acrylonitrile copolymers, copolymers of styrene and higher alcohol esters of acrylic acid and/or higher alcohol esters of methacrylic acid are preferably used in terms of ease of spinning and ease of dissolution and removal. . Furthermore, it is possible to obtain fibers with a high draw ratio and high strength.
Higher alcohol ester of tyrene and acrylic acid and/or
Alternatively, a copolymer of methacrylic acid with a higher alcohol ester is more preferably used.
また、該極細繊維を枝分かれしやすくするという点で、
結合成分あるいは溶解除去成分にポリエチレングリコー
ルなどの重合体を0.5〜60重量係混合して用いるこ
とが好ましい。かかる極細繊維形成型繊維の繊度は特に
限定されるものではないが、紡糸における安定性、シー
ト形成のしやすさなどから0.6〜10デニールのもの
が好ましい。In addition, in terms of making the ultrafine fibers easier to branch,
It is preferable to mix 0.5 to 60 weight percent of a polymer such as polyethylene glycol with the binding component or the dissolution/removal component. The fineness of such microfiber-forming fibers is not particularly limited, but is preferably from 0.6 to 10 deniers from the viewpoint of stability during spinning and ease of sheet formation.
本発明の銀面層における極細繊維は、繊度が005デニ
ール以下のものが好ましい。0.05デニールよシ太い
場合は、繊維の剛性が過大で銀面層の柔軟性や表面のし
わ形態が損われるはかシでなく揉みなどによシ亀裂が発
生しやすく表面に凹凸が発生したシして緻密でしなやか
な銀面層の形成がむつかしい。好ましくは0.05デニ
ール以下。The ultrafine fibers in the grain layer of the present invention preferably have a fineness of 005 denier or less. If the fiber is thicker than 0.05 denier, the stiffness of the fiber is too high and the flexibility of the grain layer and the form of wrinkles on the surface are impaired. Cracks are likely to occur due to rubbing, etc., resulting in unevenness on the surface. It is difficult to form a dense and supple grain layer. Preferably 0.05 denier or less.
更に好ましくはo、 o o iデニール以下の極細繊
維を用いることによって、はじめて繊維どうしの交絡が
緻密にでき、平滑性がよくしなやかで、亀裂が発生しに
くく手になじみのよい銀面層を有する皮革様シート物が
得られる。More preferably, by using ultrafine fibers with a denier of o or o o i or less, the fibers can be intertwined closely for the first time, and have a grain layer that is smooth and pliable, does not easily crack, and is comfortable in the hand. A leather-like sheet material is obtained.
本発明の皮革様シート物の銀面層における繊維構造は極
細繊維および/′!、たはその束が相互に緻密に交絡し
ていることが必要である。すなわち繊維の交絡密度が高
いということである。繊維の交絡密度を測る一つの方法
として、後述する繊維交絡点間距離を測定する方法があ
るが、銀面層の繊維は、この方法での測定値が200μ
以下の交絡密度を有していることが必要である。この値
が200μよシ大きい構造のもの、たとえば繊維の交絡
をニードルパンチだけで行なった絡みの少ない繊維構造
のもの、あるいは極細繊維またはその束が単に面配列し
た構造のもの、あるいはまた極細繊維寸たはその束が基
材表面に毛羽状に密生しこれをねかせて造園した構造の
ものは、繊維の交絡がほとんどないかまたは少ないため
、擦過、揉み、<シ返しせんだん断力などを受けたとき
1表面が毛羽立ったり亀裂が発生したりしやすいため好
ましくない。こうした欠点をなくすためには。The fiber structure in the grain layer of the leather-like sheet of the present invention is comprised of ultrafine fibers and /'! , or their bundles must be closely intertwined with each other. In other words, the fiber entanglement density is high. One way to measure the fiber entanglement density is to measure the distance between fiber entanglement points, which will be described later.
It is necessary to have the following entanglement density. This value is larger than 200 μ, for example, a fiber structure with little entanglement in which the fibers are entangled only by needle punching, or a structure in which ultrafine fibers or bundles thereof are simply arranged in a plane, or another ultrafine fiber size. Landscaping structures in which fibers or their bundles grow densely like fluff on the surface of the base material and are left to rest have little or no intertwining of the fibers, and are therefore susceptible to abrasion, kneading, and shearing force. When this happens, the surface tends to become fluffy and cracks are likely to occur, which is undesirable. In order to eliminate these shortcomings.
繊維交絡点間距離は200μ以下であることが必要であ
る。100μ以下の場合けよシ好ま−しい結果が得られ
る。The distance between fiber entanglement points must be 200μ or less. If it is less than 100μ, favorable results can be obtained.
ここで、繊維交絡点間距離とは、つきの方法でめた値の
ことであシ、繊維の交絡の緻密さを示す一つの尺度とし
て値が小さいほど交絡が緻密であることを示すものであ
る。第1図は銀面層における構成繊維を表面側から観察
したときの構成繊維の拡大模式図である。構成繊維をf
1 + f2 + fx r・・・・・・・・・とし
、そのうちの任意の2本の繊維f、、f2が交絡する点
を alとし、aIで上になっている繊維f、が他の繊
維の下になる形で交差する点までたどっていき、その交
差した点をa、(f、とf、の交絡点)とする。同様に
J l a41 aB +・・・・・・・・・・・・と
する。Here, the distance between fiber entanglement points is a value determined by the method of Tsuki, and is a measure of the density of intertwining of fibers, and the smaller the value, the more dense the intertwining is. . FIG. 1 is an enlarged schematic diagram of the constituent fibers in the grain layer when observed from the surface side. The constituent fibers are f
1 + f2 + fx r......, and the point where any two fibers f, f2 are intertwined is al, and the fiber f on the top at aI is Trace the fibers to the point where they intersect under the fibers, and let the intersecting point be a, (intersection point of f and f). Similarly, it is assumed that J l a41 aB + .
つぎにこうしてめた交絡点の間の直線水平距離a、、
a、、 a、a、、 a、a、、 a、a、、 a、a
6. a6a、、 a7a、。Next, the straight horizontal distance a between the intersecting points thus determined,
a,, a, a,, a, a,, a, a,, a, a
6. a6a,, a7a,.
a3a1a、a、Ia、aq、a9a6.・・・・・・
・・・・・・を測定し、これら多数の測定値の平均値を
めこれを繊維交絡点間距離とする。a3a1a, a, Ia, aq, a9a6.・・・・・・
. . . are measured, and the average value of these many measured values is taken as the distance between fiber entanglement points.
また、銀面層の下層は極細繊維束が主体に交絡しており
、銀面層の極細繊維および/またはその束は該下層の極
細繊維束が枝分かれしてさらに緻密に交絡したものであ
シ、銀面層と該下層では繊維は実質的に連続しておシ、
かつ該両層の境界は枝分かれの程度が連続的に変化した
繊維構造のものは、一体感のある風合のゴルフ手袋が得
られ銀面層と下層が剥離することがないことから好まし
く用いられる。ここで、銀面層の極細繊維束の束の太さ
は全ての束が同じである必要はなく、該下層の束の太さ
にくらべできるだけ細い(束に含まれる繊維の本数が下
層の束にくらべできるだけ少ない)方がシート物の表面
に凹凸が発生しにくく好ましい。また、基材に不織布を
使用した従来の皮革様シート物からのゴルフ手袋は基材
が繊維だけからなるものでは外力によって伸びやすく変
形が塑性的であるため、もとの形にもどシに<<。In addition, the lower layer of the grain layer is mainly composed of ultrafine fiber bundles, and the grain layer's ultrafine fibers and/or their bundles are branched and more densely intertwined ultrafine fiber bundles of the lower layer. , the fibers are substantially continuous in the grain layer and the lower layer,
In addition, a fiber structure in which the degree of branching continuously changes at the boundary between the two layers is preferably used because a golf glove with a unified feel can be obtained and the grain layer and the lower layer will not peel off. . Here, the thickness of the ultrafine fiber bundles in the grain layer does not need to be the same for all bundles, but is as thin as possible compared to the thickness of the bundle in the lower layer (the number of fibers included in the bundle is smaller than that in the bundle in the lower layer). It is preferable that the surface of the sheet is less likely to have unevenness on the surface of the sheet. In addition, golf gloves made from conventional leather-like sheets that use nonwoven fabric as a base material are easy to stretch due to external force and deform plastically when the base material is made only of fibers, so it is difficult to return to the original shape. <.
これを防止することから基材に樹脂が付与されていた。To prevent this, resin has been applied to the base material.
しかし、極細繊維および/−1:たけその束が緻密に交
絡した繊維構造を有する本発明のゴルフ手袋は、該下層
部に樹脂が付与されてなくても異常に伸びることは少な
く、形態保持性が良好である。このことも本発明の大き
な特徴である。However, the golf glove of the present invention, which has a fiber structure in which ultrafine fibers and bundles of /-1: bamboo shoots are densely intertwined, does not stretch abnormally even if resin is not added to the lower layer, and has good shape retention. is good. This is also a major feature of the present invention.
もち、うん、該下層にはポリウレタンニジストマーなど
の樹脂が付与されていてもよく、樹脂付量はシート、7
物の使用目的によって異なる。ゴルフ手袋用として用い
る場合は繊維の重量に対し0〜50部の付量が好′まし
い。銀面層に用いる樹脂は、たとえば、ポリアミド、ポ
リエステル、ポリ塩化ビニル、ポリアクリル酸エステル
共重合体、ポリウレタン、ネオプレン、スチレンブタジ
ェン共重体。Yes, a resin such as polyurethane distomer may be applied to the lower layer, and the amount of resin applied is about 7
It depends on the purpose of use of the object. When used for golf gloves, the amount applied is preferably 0 to 50 parts based on the weight of the fiber. Examples of the resin used for the silver layer include polyamide, polyester, polyvinyl chloride, polyacrylate copolymer, polyurethane, neoprene, and styrene-butadiene copolymer.
アクリロニトリルブタジェン共重合体、ポリアミノ酸、
ポリアミノ酸ポリウレタン共重合体、シリコン樹脂など
の合成樹脂または天然高分子樹脂。Acrylonitrile butadiene copolymer, polyamino acid,
Synthetic resins or natural polymer resins such as polyamino acid polyurethane copolymers and silicone resins.
またはこれら樹脂の混合物などである。更に必要吟よっ
ては可塑剤、充填剤、安定剤、顔料、染料。Or a mixture of these resins. Furthermore, depending on the requirements, plasticizers, fillers, stabilizers, pigments, and dyes.
架橋剤等を添加してもよい。ポリウレタン樹脂またはこ
れに他の樹脂や添加剤を加えたものは、特に柔軟な風合
や感触をもち耐屈曲性のより銀面層が得られるため好ま
しく用いられゐ。銀面層の樹脂の付着構造については格
別な限定はなく目的によって変わりうるが、柔軟性やや
わらかな感触が特に要求される場合は、嫁面層の表面に
近くなるにつれて樹脂が多く付着した構造のもの、銀面
層の最表面のごく薄い層の樹脂付量が特に多く、その他
は全く樹脂が付着していないか付着していてもわずかの
量であるような構造のもの、あるいは。A crosslinking agent or the like may be added. Polyurethane resins or polyurethane resins to which other resins or additives are added are preferably used because they provide a grain layer with particularly soft texture and feel and good bending resistance. The resin adhesion structure of the silver layer is not particularly limited and may vary depending on the purpose, but if flexibility and soft feel are particularly required, a structure in which more resin is adhered closer to the surface of the bride layer may be used. or those with a structure in which the very thin layer on the outermost surface of the grain layer has a particularly large amount of resin attached, and the rest has no resin attached at all or only a small amount if it is attached.
表面部分の樹脂は非多孔質でそれ以下は多孔質である構
造のものなどが方寸しい。′!!た。耐傷性の特に高い
ことが要求される場@″は、銀面層の空隙部分にほとん
どすきまなく樹脂が充填された構造のものが好ましい。It is preferable to have a structure in which the resin on the surface is non-porous and the rest is porous. ′! ! Ta. In cases where particularly high scratch resistance is required, a structure in which the voids in the grain layer are filled with resin almost without gaps is preferred.
本発明のゴルフ手袋を製造する方法としては。As a method for manufacturing the golf glove of the present invention.
まず該極細繊維形成型繊維をたとえば特公昭44−18
369号公報に示された紡糸装置で製造し。First, the ultrafine fiber-forming fiber is
Manufactured using the spinning device shown in Japanese Patent No. 369.
ステープルにした後カード、クロクラツノく−を通して
ウェブを形成し、さらにこれにニードル、・<ンチを行
ない該極細繊維形成型繊維を交絡させ繊維シートを形成
する。または、該極細繊維形成型繊維の紡糸に引き続い
て延伸を行ない金網上にランダムに載置し、得られたウ
ェブに前記と同様にニードルパンチを行ない繊維シート
を形成する。あるいは、普通繊維または別の極細繊維形
成型繊維からなる不織布、織布9編布に該極細繊維形成
型繊維を載置し、からませ不離一体にして繊維シートを
形成する。つぎに、こうして得られた繊維シートに高床
流体流を接触させて銀面層に相当する部分を極細繊維お
よび/またはその束に枝分かれさせると同時に緻密に交
絡させる。ここでいう流体とは、液体あるいは気体であ
シ、特別な場合は。After being stapled, a web is formed by passing through a card and a black horn, which is then subjected to needling and punching to intertwine the ultrafine fiber-forming fibers and form a fiber sheet. Alternatively, following the spinning of the microfiber-forming fibers, they are stretched and placed randomly on a wire mesh, and the obtained web is needle punched in the same manner as described above to form a fiber sheet. Alternatively, the ultra-fine fiber-forming fibers are placed on a non-woven fabric or woven nine-knit fabric made of ordinary fibers or other ultra-fine fiber-forming fibers, and are entangled and inseparably integrated to form a fiber sheet. Next, the fiber sheet obtained in this manner is brought into contact with a raised fluid stream to branch the portion corresponding to the grain layer into ultrafine fibers and/or bundles thereof, and at the same time to entangle them densely. The fluid here refers to liquid or gas, in special cases.
きわめて微細な固体を含むものであってもよいが。It may contain extremely fine solids.
取り扱いやすさ、コスト、流体としての衝突エネルギー
量の点から水が最も好ましく用いられる。Water is most preferably used in terms of ease of handling, cost, and amount of collision energy as a fluid.
さらに目的に応じて、該極細繊維形成型繊維の一部成分
を溶解可能な種々の有機溶剤あるいは水酸化ナトリウム
などのアルカリまたは酸の水溶液なども使用できる。こ
れらの流体を加圧し、孔径の小さいノズルあるいは間隔
のせまいスリットから噴射させ高速の柱状流あるいはカ
ーテン状流とし。Furthermore, depending on the purpose, various organic solvents capable of dissolving some components of the ultrafine fiber-forming fibers, or aqueous solutions of alkalis or acids such as sodium hydroxide can also be used. These fluids are pressurized and injected through small-diameter nozzles or narrowly spaced slits to create a high-speed columnar flow or curtain-like flow.
繊維シートに接触させ繊維の枝分かれおよび交絡を行な
う。液体にかける圧力は、該極細繊維形成型繊維あるい
は極細繊維束の枝分かれのしやすさによって異なシ、枝
分かれしやすい繊維では、5〜7047Cm2の比較的
低圧でよいが、枝分かれしにくい繊維では、70〜30
0147cm” の高、圧が必要である。捷だ、接触回
数をふやすことによp枝分かれおよび交絡の程度を高め
ることも可能であシ。The fibers are brought into contact with the fiber sheet to branch and entangle the fibers. The pressure applied to the liquid varies depending on the ease of branching of the ultrafine fiber-forming fibers or ultrafine fiber bundles.For fibers that are easy to branch, a relatively low pressure of 5 to 7047 cm2 may be sufficient, but for fibers that are difficult to branch, a relatively low pressure of 70 cm2 is sufficient. ~30
A high pressure of 0.147 cm" is required. However, it is also possible to increase the degree of p-branching and entanglement by increasing the number of contacts.
接触のたびごとに圧力を変化させてもよい。しかる後、
使用した該極細繊維形成型繊維を極細化するのに必要と
される場合は、該極細繊維形成型繊維の一部成分を溶解
する溶剤で得られた繊維シートを処理し該一部成分を溶
解除去する。The pressure may be varied with each contact. After that,
If necessary to make the used ultrafine fiber-forming fibers ultrafine, the obtained fiber sheet is treated with a solvent that dissolves some components of the ultrafine fiber-forming fibers to dissolve some of the components. Remove.
捷た。必要に応じてポリウレタンニジストマーなどの樹
脂の溶液又は分散液を含浸し湿式又は乾式によって凝固
させる。ここで、高速流体流で処理する前に該一部成分
を溶解除去してもよく、この場合は、該一部成分め溶解
除去によって繊維シートの該極細繊維形成型繊維が極細
繊維の束に変成されているため、低い流体圧で容易にし
かも高度に枝分かれおよび交絡させることができること
から好ましい方法である。また、該一部成分の溶解除去
の工程の前と後で高速流体流の処理を行なってもよい0
また。樹脂を付与する工程は、前記のほかに、高速流体
流の処理工程と該繊維の一部成分の溶解除去工程の間に
もってくることが可能で。I cut it. If necessary, it is impregnated with a solution or dispersion of a resin such as polyurethane disstomer and solidified by a wet or dry method. Here, the part of the component may be dissolved and removed before the treatment with the high-speed fluid flow. In this case, by dissolving and removing the part of the component, the ultrafine fiber-forming fibers of the fiber sheet become a bundle of ultrafine fibers. This is a preferred method because it is metamorphosed and can be easily and highly branched and entangled at low fluid pressures. In addition, high-speed fluid flow treatment may be performed before and after the step of dissolving and removing the partial components.
Also. In addition to the above steps, the step of applying the resin can be carried out between the high-speed fluid flow treatment step and the step of dissolving and removing some components of the fibers.
この場合は、該一部成分の溶解除去に使用する溶剤で付
与した樹脂が溶解しないことが必要であるが、得られた
繊維シートの極細繊維束と樹脂との間に該一部成分が存
在していた空間ができ相反の動きに自由度が増すため風
合を柔軟にするのに好ましい方法である。一方、樹脂を
伺与した後で高速流体流の処理を行なうことは、樹脂の
付量が多いときは繊維が樹脂で束縛されているため枝分
かれおよび交絡がほとんど行なわれず、好ましい方法と
はいえない。しかる後、得られた繊維シートの極細繊維
および/またはその束が交絡した層へ前記した銀面層用
樹脂の溶液又は分散液をリバースロールコーティング、
クラビアコーティング。In this case, it is necessary that the applied resin is not dissolved by the solvent used to dissolve and remove the partial component, but the partial component must exist between the resin and the ultrafine fiber bundle of the obtained fiber sheet. This is the preferred method for making the texture flexible, as it frees up space and increases the degree of freedom for opposing movements. On the other hand, performing high-speed fluid flow treatment after applying the resin is not a desirable method because when a large amount of resin is applied, the fibers are bound by the resin, so branching and entanglement hardly occur. . After that, the solution or dispersion of the resin for the grain layer described above is applied to the layer of the obtained fiber sheet in which the ultrafine fibers and/or their bundles are intertwined, by reverse roll coating.
Clavia coating.
ナイフコーティング、スリットコーティング、スプレー
などの方法で付与し、湿式又は乾式によって凝、□□、
。〜7.つあるいは、−1面に重ね゛合わせ加圧必要に
応じて加熱し、繊維と樹脂とを一体化せしめると同時に
表面の平滑化を行なう。Apply by knife coating, slit coating, spraying, etc., and harden by wet or dry method.
. ~7. Alternatively, the fibers and resin are stacked on the -1 side, pressed, and heated as necessary to integrate the fibers and resin and at the same time smooth the surface.
ここで、樹脂を付与する前に繊維シートにプレスなどの
処理を行ない表面の平滑化することも好ましい方法であ
る。このとき表面にシボ模様のあるエンボスロールある
いはシボ賦型シートラ使用すると一体化、平滑化とシボ
賦型が同時に行なえるため方寸しい。さらに必要に応じ
て、仕上げ剤塗布、染色、揉みなどの処理を行なっても
よい1゜本発明のゴルフ手袋において、ドレープ係数は
0、3〜0.7が好ましい。当該範囲内では、耐久性。Here, it is also a preferable method to subject the fiber sheet to a treatment such as pressing to smooth the surface before applying the resin. At this time, it is difficult to use an embossing roll with a textured surface or a texture-forming sheet roll because it allows integration, smoothing, and texture-forming to be performed at the same time. Furthermore, if necessary, treatments such as applying a finishing agent, dyeing, and rubbing may be performed.In the golf glove of the present invention, the drape coefficient is preferably 0.3 to 0.7. Within this range, durability.
フィツト性ともに極めて良好なものが得られる。An extremely good fit can be obtained.
ここでドレープ係数とは、J工s−:c、−1096の
方法により測定した値である。Here, the drape coefficient is a value measured by the method of J.E.S-:c, -1096.
ドレープ性は、構成される極細繊維発生型繊維の枝分か
れおよび交絡の程度、バインダー樹脂の有無およびその
付与方法(乾式または湿式)、バインダー樹脂の付与量
9種類、銀面層用制脂の付与量2種類等を適宜選択する
ことによってコントロールが可能である1、
また9本発明のゴルフ用手袋には、50 g 70m”
荷重(丸型)で0.6〜1.5mm厚さのものが方寸し
い。Drapability is determined by the degree of branching and entanglement of the ultra-fine fiber-generating fibers, the presence or absence of binder resin and its application method (dry or wet), the amount of 9 types of binder resin applied, and the amount of antigreasing agent for the grain layer. The golf gloves of the present invention can be controlled by appropriately selecting two types, etc. 1, 9 The golf gloves of the present invention include
A load (round shape) with a thickness of 0.6 to 1.5 mm is suitable.
さらに本発明のゴルフ手袋は、上記人工皮革の銀面層を
表にして第2図の如く縫製したものである。銀面層が表
になっていないと、従来のスェード調人工皮革と同様、
滑べりやすいフィツトしにくい性質となるので好ましく
ない。指部に穴をあけたものは通気や汗を出す効果があ
シ方寸しい。Furthermore, the golf glove of the present invention is made by sewing the above-mentioned artificial leather with the grain layer facing up as shown in FIG. If the grain layer is not exposed, like traditional suede-like artificial leather,
It is undesirable because it becomes slippery and difficult to fit. Those with holes in the fingers are very effective at allowing ventilation and sweat to escape.
以下に示す実施例は1本発明をより明確にするためのも
のであって9本発明けこれに限定されるものではない。The examples shown below are for the purpose of clarifying the present invention more clearly, and the present invention is not limited thereto.
実施例1
ポリスチレン95部とポリエチレングリコール5部の混
合物を結合成分として45部、極細繊維成分としてポリ
エチレンテレフタレート55部なる割合で1フイラメン
ト中に極めて多数本の極雅繊維が含まれるごとき形態の
高分子相互配列体繊維の3.8デニール、51mmのも
のを用いて実施例1と同様の方法で不織布をつくった。Example 1 A polymer in such a form that one filament contains an extremely large number of Kyokuga fibers in a ratio of 45 parts of a mixture of 95 parts of polystyrene and 5 parts of polyethylene glycol as a binding component and 55 parts of polyethylene terephthalate as an ultrafine fiber component. A nonwoven fabric was made in the same manner as in Example 1 using 3.8 denier, 51 mm mutually arranged fibers.
この不織布の目付は400 g/ m”、厚みij 2
.0 ml11であった。この不織布の片面に、孔径0
.1 mmの孔が0.6 mmピッチで一列に並んだノ
ズルを用いて1004/♂の圧力で噴射させた水の柱状
流を接触させ、同じ条件で5回、圧力を30kg/c”
に下げて2回の処理を行なった。さらに95°Cの熱
水中に入れ収縮処理とマングルによるニップを行なった
。得られた交絡不織布は、厚みが約1.2圓に減少し、
水流処理繊維から枝分かれした平均繊度約0. OD
1デニールの極細繊維およびその束が主体に緻密に密度
高く交絡しており、その表面は凹凸のきわめて少ないも
のであった。The basis weight of this non-woven fabric is 400 g/m”, thickness ij 2
.. It was 0 ml11. One side of this nonwoven fabric has a pore size of 0
.. A columnar flow of water injected at a pressure of 1004/♂ using a nozzle with 1 mm holes arranged in a row at a pitch of 0.6 mm was brought into contact, and the pressure was increased to 30 kg/c five times under the same conditions.
The treatment was carried out twice at a lower temperature. Furthermore, it was placed in hot water at 95°C and subjected to a shrinkage treatment and a nip using a mangle. The thickness of the obtained interlaced nonwoven fabric was reduced to about 1.2 mm,
The average fineness of branches branched from water-treated fibers is approximately 0. O.D.
The 1-denier ultrafine fibers and their bundles were mainly densely and densely intertwined, and the surface had very few irregularities.
次に、0.8++nnにスライスした後、水流処理した
側の表層にポリウレタンの溶液にカーボンブラックと染
料を添加した塗料をグラビアコータで付与し、乾燥、プ
レスして一体化して複合体を形成しシボ賦型を行なった
。更に、トリクロルエチレンを用いてポリスチレンとポ
リエチレングリコールの溶解除去を行ない5反対面はノ
(フイングを行ない極細繊維を毛羽立たせ、ついで分散
染料を用いて120’O高温染色を行ない通常の、仕上
げ加工を行なった。厚みは約0.7 mmであった。Next, after slicing into 0.8++nn, a paint made by adding carbon black and dye to a polyurethane solution was applied to the surface layer of the water-treated side using a gravure coater, dried and pressed to form a composite. Grain shaping was performed. Furthermore, polystyrene and polyethylene glycol were dissolved and removed using trichlorethylene, and the other side was blown to fluff the ultrafine fibers, and then dyed at a high temperature of 120'O using a disperse dye and finished as usual. The thickness was approximately 0.7 mm.
さらに本発明の人工皮革および市販の立毛タイプのスェ
ード調人工皮革と薄いポリウレタン層を表面銀面として
もつ釦付人工皮革の6者から、第2図のようなゴルフ手
袋を縫製したところ、第1表のように本発明の人工皮革
ゴルフ手袋は最も優れた性質、特にグリップとのフィツ
ト性を示した。Furthermore, when golf gloves as shown in Fig. 2 were sewn from six materials: the artificial leather of the present invention, a commercially available napped type suede-like artificial leather, and a buttoned artificial leather having a thin polyurethane layer as a silver surface, golf gloves as shown in Fig. 1 were sewn. As shown in the table, the artificial leather golf glove of the present invention exhibited the most excellent properties, especially the fit with the grip.
第 1 表
この本発明のゴルフ手袋の銀面層のポリウレタンおよび
仕上げ剤を除去し構成繊維の平均繊維交絡点間距離を測
定したところ98μであった。Table 1 After removing the polyurethane and finishing agent from the grain layer of the golf glove of the present invention, the average distance between fiber entanglement points of the constituent fibers was measured and found to be 98μ.
また、額施例のドレープ係数は0.45であった。Further, the drape coefficient of the frame example was 0.45.
実施例2
2−エチルへキシルアクリレ−)20部、スチレン80
部の割合で共重合させたビニール系ポリマ(以下AS樹
脂という)を結合成分として60部、極細繊維成分とし
てナイロン6が40部からなる割合で1フイラメント中
に16本の島成分を有し、さらにその酸成分中に0.0
01〜0.0006デニールの極細繊維成分が多数台ま
れる形態の特公昭47−37648に示されたごとき高
分子相互配列体繊維の40デニール、51mmのステー
プルを用いてカード・クロスラッパーを通してウエブヲ
形成し、しかる後フックの数が1個のニードルを用いて
ニードルパンチをして該高分子相互配列体繊維を絡合さ
せ不織布をつくった。不織布の目付は405 g/m’
、見掛密度は0.20 g/Cm”であった。Example 2 20 parts of 2-ethylhexyl acrylate, 80 parts of styrene
60 parts of vinyl polymer (hereinafter referred to as AS resin) copolymerized in a proportion of 60 parts as a bonding component and 40 parts of nylon 6 as an ultrafine fiber component, with 16 island components in one filament, In addition, 0.0
Forming a web through a card cross wrapper using a 40 denier, 51 mm staple of polymeric mutual array fibers as shown in Japanese Patent Publication No. 47-37648 in which a large number of ultrafine fiber components of 0.01 to 0.0006 denier are mounted. After that, needle punching was performed using a needle with one hook to entangle the polymeric mutually arranged fibers to produce a nonwoven fabric. The basis weight of the non-woven fabric is 405 g/m'
, the apparent density was 0.20 g/Cm''.
孔径0.1 mmの孔が孔の中心間距離0.6rrrm
のピッチで一列に並んだノズルからノズルを揺動させな
がら、その表面に高速の噴射水を接触さぜ、第2表の4
種のシー!・をつくった。得られたシートけ表層の高分
子相互配列体繊維が極細繊維やその束に枝分かれしてお
り、かつ相互に緻密に交絡した繊維構造を有するもので
あった。For holes with a hole diameter of 0.1 mm, the distance between the centers of the holes is 0.6rrrm.
While shaking the nozzles from the nozzles lined up in a row at a pitch of
Seed sea!・Created. The polymeric mutually arranged fibers in the surface layer of the obtained sheet were branched into ultrafine fibers or bundles thereof, and had a fiber structure in which they were densely intertwined with each other.
つぎに第2表中りのシートのみにポリエチレンアジペー
トとポリブチレンアジペートとの混合シオールトp+p
’−ジフェニルメタンジイソシア坏−トのプレポリマー
をエチレングリコールで鎖伸長して得られたポリウレタ
ンの7チジメチルホルムアミド(以下DMFという)溶
液を含浸し表面に付着した液をスフレイパーで除去して
水中へ導入して凝固した。しかる後8 D ’cの熱水
中で十分洗浄しDMFを除去した。Next, only the sheets in Table 2 are mixed thiolt p+p of polyethylene adipate and polybutylene adipate.
A prepolymer of '-diphenylmethane diisocyanate was chain-extended with ethylene glycol, and the polyurethane was impregnated with a 7-tidimethylformamide (hereinafter referred to as DMF) solution. It was introduced and solidified. Thereafter, it was sufficiently washed in hot water at 8 D'c to remove DMF.
つぎに、これら4種のシートの表面から、含浸に用いた
ポリウレタンと組成は同じであるが、硬さをや゛や硬く
したポリウレタンの10%溶液に顔料を添加した溶液を
グラビアコータで伺力し乾燥後加熱エンボスロールに通
してプレスし皮革様シホ模様を型押しした。ついで、ト
リクロルエチレン中につけ、浸漬、絞液をくシ返し、A
S樹脂をほぼ完全に抽出除去し、その後乾燥を行なって
。Next, from the surface of these four types of sheets, a solution of pigment added to a 10% solution of polyurethane, which has the same composition as the polyurethane used for impregnation but is slightly harder, was applied using a gravure coater. After drying, it was pressed through a heated embossing roll to emboss a leather-like grain pattern. Then, immerse it in trichlorethylene, immerse it, and twirl the squeezed solution.
The S resin was almost completely extracted and removed, and then dried.
残留トリクロルエチレンを蒸発除去した0さらに常圧で
液流染色機を用いて染色し9通常の方法で仕上げ加工を
行なった。厚みは4種のシートとも約0.5工であった
。Residual trichlorethylene was removed by evaporation, and then dyed using a jet dyeing machine at normal pressure.9 Finishing was carried out in a conventional manner. The thickness of all four types of sheets was approximately 0.5 mm.
これら4種のシートのドレープ係数と、これらを縫製し
たゴルフ手袋のグリップへのフィツト性。The drape coefficients of these four types of sheets and the fit to the grip of golf gloves sewn from these sheets.
外観および耐久性は次の通シであった。The appearance and durability were as follows.
第 2 表Table 2
第1図は本発明の人工皮革ゴルフ手袋の表面の銀面層に
おける構成繊維の表面側から観察した時の構成繊維の拡
大模式図である。
第2図は本発明の人工皮革ゴルフ手袋の概念図である。
特許出願人 東 し 株 式 会 社
中11刀
へΣ )6
竹7出FIG. 1 is an enlarged schematic view of the constituent fibers in the grain layer on the surface of the artificial leather golf glove of the present invention when observed from the surface side. FIG. 2 is a conceptual diagram of the artificial leather golf glove of the present invention. Patent applicant Higashi Shi Co., Ltd. Company 11th sword Σ ) 6 Bamboo 7 out
Claims (1)
び/″!、たはその束の繊維交絡点間距離が200ミク
ロン以下である繊維構造体と、その空隙部分に存在する
樹脂とから主としてなる複合体によって形成された銀面
層を少なくとも片面に有し、かつ該銀面層の下層は極細
繊維束が主体に交絡しておシ、銀面層は該下層の極細繊
維束が枝分かれしゝた極細繊維および/またはその束が
主体となっておシ、該下層と銀面層における繊維は実質
的に連続しておυ、更に該両層の境界は枝分かれの程度
が連続的に変化している銀材人工皮革の銀面層を表にし
て縫製してなることを特徴とするゴルフ用人工皮革手袋
。(1) A composite mainly consisting of ultrafine fibers of 0.05 denier or less and /''!, or a fiber structure in which the distance between fiber entanglement points of a bundle thereof is 200 microns or less, and a resin existing in the voids. At least one side has a grain layer formed by the grain, and the lower layer of the grain layer is mainly composed of ultrafine fiber bundles intertwined with each other, and the grain layer has branched microfiber bundles in the lower layer. The fibers are mainly composed of ultrafine fibers and/or bundles thereof, and the fibers in the lower layer and the grain layer are substantially continuous, and the degree of branching at the boundary between the two layers continuously changes. This artificial leather glove for golf is made by sewing a silver material artificial leather with the silver layer facing up.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58114303A JPS607876A (en) | 1983-06-27 | 1983-06-27 | Artificial leather glove for golf |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58114303A JPS607876A (en) | 1983-06-27 | 1983-06-27 | Artificial leather glove for golf |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS607876A true JPS607876A (en) | 1985-01-16 |
| JPH0137957B2 JPH0137957B2 (en) | 1989-08-10 |
Family
ID=14634489
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP58114303A Granted JPS607876A (en) | 1983-06-27 | 1983-06-27 | Artificial leather glove for golf |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS607876A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6211116U (en) * | 1985-07-03 | 1987-01-23 | ||
| JP2009142529A (en) * | 2007-12-17 | 2009-07-02 | A Plan Kk | Sports glove |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS533501A (en) * | 1976-06-27 | 1978-01-13 | Daiichi Kasei | Production of artificial leather |
| JPS5758463A (en) * | 1980-09-26 | 1982-04-08 | Canon Inc | Picture pattern converter |
| JPS5813785A (en) * | 1981-07-15 | 1983-01-26 | 旭化成株式会社 | Artificial leather with silver |
-
1983
- 1983-06-27 JP JP58114303A patent/JPS607876A/en active Granted
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS533501A (en) * | 1976-06-27 | 1978-01-13 | Daiichi Kasei | Production of artificial leather |
| JPS5758463A (en) * | 1980-09-26 | 1982-04-08 | Canon Inc | Picture pattern converter |
| JPS5813785A (en) * | 1981-07-15 | 1983-01-26 | 旭化成株式会社 | Artificial leather with silver |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6211116U (en) * | 1985-07-03 | 1987-01-23 | ||
| JP2009142529A (en) * | 2007-12-17 | 2009-07-02 | A Plan Kk | Sports glove |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0137957B2 (en) | 1989-08-10 |
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