JPH03161501A - Production of glove having electrical insulation property - Google Patents
Production of glove having electrical insulation propertyInfo
- Publication number
- JPH03161501A JPH03161501A JP1302971A JP30297189A JPH03161501A JP H03161501 A JPH03161501 A JP H03161501A JP 1302971 A JP1302971 A JP 1302971A JP 30297189 A JP30297189 A JP 30297189A JP H03161501 A JPH03161501 A JP H03161501A
- Authority
- JP
- Japan
- Prior art keywords
- glove
- rubber latex
- latex
- cloth
- gloves
- 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
- 238000004519 manufacturing process Methods 0.000 title claims description 7
- 238000010292 electrical insulation Methods 0.000 title abstract 3
- 229920000126 latex Polymers 0.000 claims abstract description 60
- 239000004816 latex Substances 0.000 claims abstract description 38
- 239000004744 fabric Substances 0.000 claims abstract description 29
- 239000007787 solid Substances 0.000 claims abstract description 14
- 239000000701 coagulant Substances 0.000 claims abstract description 12
- 229920006173 natural rubber latex Polymers 0.000 claims abstract description 11
- 238000007598 dipping method Methods 0.000 claims abstract description 9
- 229920003049 isoprene rubber Polymers 0.000 claims abstract description 9
- 229920001971 elastomer Polymers 0.000 claims description 13
- 239000005060 rubber Substances 0.000 claims description 13
- 238000001035 drying Methods 0.000 claims description 6
- 238000010073 coating (rubber) Methods 0.000 abstract description 12
- 229920000642 polymer Polymers 0.000 abstract description 2
- 239000002685 polymerization catalyst Substances 0.000 abstract description 2
- 230000000379 polymerizing effect Effects 0.000 abstract description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 17
- 238000000034 method Methods 0.000 description 10
- 239000003795 chemical substances by application Substances 0.000 description 8
- 239000011248 coating agent Substances 0.000 description 8
- 238000000576 coating method Methods 0.000 description 8
- 238000004073 vulcanization Methods 0.000 description 6
- 238000005406 washing Methods 0.000 description 6
- 239000000047 product Substances 0.000 description 5
- -1 alkyl lithium Chemical compound 0.000 description 4
- 238000013329 compounding Methods 0.000 description 4
- 239000006260 foam Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 244000043261 Hevea brasiliensis Species 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 229920003052 natural elastomer Polymers 0.000 description 3
- 229920001194 natural rubber Polymers 0.000 description 3
- 239000012744 reinforcing agent Substances 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- 125000005234 alkyl aluminium group Chemical group 0.000 description 2
- 238000005452 bending Methods 0.000 description 2
- ZCCIPPOKBCJFDN-UHFFFAOYSA-N calcium nitrate Chemical compound [Ca+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O ZCCIPPOKBCJFDN-UHFFFAOYSA-N 0.000 description 2
- 239000005018 casein Substances 0.000 description 2
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 2
- 235000021240 caseins Nutrition 0.000 description 2
- 230000015271 coagulation Effects 0.000 description 2
- 238000005345 coagulation Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 229920001821 foam rubber Polymers 0.000 description 2
- 229920001084 poly(chloroprene) Polymers 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 206010014405 Electrocution Diseases 0.000 description 1
- 241000282326 Felis catus Species 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 230000003712 anti-aging effect Effects 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 235000015115 caffè latte Nutrition 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- 229940067606 lecithin Drugs 0.000 description 1
- 235000010445 lecithin Nutrition 0.000 description 1
- 239000000787 lecithin Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229920003008 liquid latex Polymers 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 239000012768 molten material Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 235000018102 proteins Nutrition 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 238000002317 scanning near-field acoustic microscopy Methods 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 239000007779 soft material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
- 229960002447 thiram Drugs 0.000 description 1
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 1
- 239000012936 vulcanization activator Substances 0.000 description 1
- 235000014692 zinc oxide Nutrition 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- NRINZBKAERVHFW-UHFFFAOYSA-L zinc;dicarbamate Chemical compound [Zn+2].NC([O-])=O.NC([O-])=O NRINZBKAERVHFW-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A41—WEARING APPAREL
- A41D—OUTERWEAR; PROTECTIVE GARMENTS; ACCESSORIES
- A41D19/00—Gloves
- A41D19/0055—Plastic or rubber gloves
- A41D19/0058—Three-dimensional gloves
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Gloves (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Abstract
Description
【発明の詳細な説明】
〈産業上の利用分野〉
本発明は耐電性手袋の製造法に関し、特に布つきで防水
性を有する耐電性手袋の製造法に関する。DETAILED DESCRIPTION OF THE INVENTION <Industrial Application Field> The present invention relates to a method for manufacturing an electrically resistant glove, and more particularly to a method for manufacturing an electrically resistant glove with cloth and having waterproof properties.
〈従来の技術〉
耐電性手袋は、電気回路作業用の手袋として用いられて
いる。電気回路作業用の手袋には、通常、下記のような
条件が要求される。<Prior Art> Electrical resistance gloves are used as gloves for working on electrical circuits. Gloves for working on electrical circuits usually meet the following requirements:
(a)指先で部品を摘んだり、引張ったりする作業が容
易であること。(a) It should be easy to pick and pull parts with your fingertips.
(b)防水性があること。(b) Be waterproof.
(Cl常時感電等を防止しうろこと。(Cl always has scales to prevent electric shock etc.
前記(111の要件を満たす為には、柔らかい素材を使
用し、薄くすること、(b)の要件を満たす為には、製
造工程中でゴムラテソクス中に浸漬する工程を採用し、
全表面に継目のない被膜を形成させること、(C)の要
件を満たす為には、水中であっても耐電性が低下しない
こと等が必要である。従来、前記(a)の要件を具体化
させようとして、メリヤス編みの伸縮性布帛からなる手
袋の全表面にゴムラテックスを薄く付着させようとする
方法、(blの要件を具体化させようとしてゴムラテッ
クス中に浸漬して継目のない被膜を全表面に形威しよう
とする方法、(Q)の要件を具体化させようとして、前
記(a).(blの要件をも考慮しつつ、天然ゴムラテ
ックス,クロロブレンゴムラテソクス,スチレンブタジ
エン共重合ゴムラテックス等を使用する方法が考えられ
、又実施されている。In order to meet the requirements of (111) above, a soft material should be used and made thin, and in order to meet the requirement of (b), a step of immersing it in rubber latex during the manufacturing process should be adopted,
In order to form a seamless film on the entire surface and to satisfy the requirement (C), it is necessary that the electrical resistance does not decrease even in water. Conventionally, in an attempt to embody the requirement (a) above, there has been a method in which a thin layer of rubber latex is applied to the entire surface of gloves made of stockinette-knit stretchable fabric. In an attempt to materialize the requirements of (Q), a method in which a seamless coating is applied to the entire surface by dipping it in latex, while also considering the requirements of (a). Methods using latex, chloroprene rubber latex, styrene-butadiene copolymer rubber latex, etc. have been considered and implemented.
〈発明が解決しようとするi!¥題〉
しかしながら、前記fan. (b)の要件を具体化さ
せる方法には、以下のような欠点があった。<The invention tries to solve i! ¥Title> However, the said fan. The method of realizing the requirement (b) had the following drawbacks.
メリヤス編みの伸縮性布帛からなる布手袋にはかなり大
きな編目の孔がある。これを手型に被装してラテックス
に浸漬すれば、ラテックスの目洩れは避けられない。ラ
テックスの目洩れは布手袋の伸縮性を阻害して使用時の
屈曲抵抗を増し、ゴム手袋の作業性を著しく阻害する。Cloth gloves made of stockinette stretch fabric have fairly large stitch holes. If this is applied to a hand mold and dipped in latex, leakage of the latex is inevitable. Latex leakage inhibits the elasticity of cloth gloves, increases bending resistance during use, and significantly impairs the workability of rubber gloves.
特に、一般の作業軍手では、手型に被装すると少な《と
も0.3〜0.5gm程度の編目の孔があり、ラテック
ス被膜自体にピンホールが生じるのは避けられない。In particular, when general work gloves are coated on a hand pattern, there are holes of at least 0.3 to 0.5 gm in mesh, and it is inevitable that pinholes will occur in the latex coating itself.
従来、ラテックス浸漬法で作或した布つき防水ゴム手袋
が実用化しにくいのは、この問題のためである。It is because of this problem that it has been difficult to put waterproof rubber gloves with cloth made by the latex dipping method into practical use.
又、前記(Clの要件を具体化させる方法には以下のよ
うな欠点があった。Furthermore, the method for realizing the requirements for Cl has the following drawbacks.
クロロプレンゴムラテックスは補強剤等を配合しなくて
も、流延して乾燥した被膜が強く、ラテンクス自体も安
定していて取扱い易いが高価格であり、又、スチレンブ
タジエン共重合ゴムラテックスは流延して乾燥した被膜
を強くするには、補強剤等を多量配合しなければならず
、その結果、ラテックスの安定性が悪くなり取扱いに<
<、被膜も外観が良好なものが得に<<、その上硬くな
る等の欠点があった。Chloroprene rubber latex has a strong coating after being cast and dried even without the addition of reinforcing agents, and the latex itself is stable and easy to handle, but it is expensive. In order to strengthen the dried film, it is necessary to add a large amount of reinforcing agent, etc. As a result, the stability of the latex deteriorates and it becomes difficult to handle.
The coating had good appearance, but it also had drawbacks such as hardness.
これに対し、天然ゴムラテソクスは補強剤等を配合しな
くても流延して乾燥した被膜が強く、ラテックス自体も
安定性があり、外観が良好な被膜が得られ易く、得られ
た被膜も柔軟であり、価格もさほど高くもない等の長所
が数多くあるため、最も多く使用されている。On the other hand, natural rubber latex has a strong coating after being cast and dried even without the addition of reinforcing agents, the latex itself is stable, it is easy to obtain a coating with a good appearance, and the resulting coating is also flexible. It is the most commonly used because it has many advantages such as not being very expensive.
天然ゴムラテソクスは、前記のように数多くの特長を有
しているけれども、常用のゴムラテックス用配合剤を使
用したコンパウンドのままで電気回路作業用の手袋に適
用した場合、水中での耐電性が悪くなる傾向が散見され
、感電事故に遭遇する虞れがあった。Although natural rubber latex has many features as mentioned above, when it is applied to gloves for working on electrical circuits as a compound using commonly used rubber latex compounding agents, it has poor electrical resistance in water. There was a tendency for this to occur, and there was a risk of electrocution.
本発明は、布手袋の目洩れないし目止めの問題を解決し
てラテックス浸漬法で薄い天然ゴム被膜を形成させ、し
かもこの天然ゴム被膜に水中でのit電性を付与しよう
とするものである。The present invention aims to solve the problem of not leaking or sealing the eyes of cloth gloves by forming a thin natural rubber coating using a latex dipping method, and also to impart IT conductivity in water to this natural rubber coating. .
く課題を解決するための手段〉
本発明は、前記課題を解決するために、手型に被装した
布手袋に凝固剤を含有せしめ、これを起泡したゴムラテ
ックスに浸漬して布手袋外面に発泡ゴムラテックスの凝
固層を形成した後、35〜65重量%の天然ゴムラテッ
クスと65〜35重量%のイソプレンゴムラテックスと
よりなるゴムラテック,スに浸漬して外面に固状ゴム被
膜を形或し、乾燥ノ
することを特徴とする耐電性手袋の製造法を提供したも
のである。Means for Solving the Problems> In order to solve the above problems, the present invention includes a cloth glove covered with a hand shape containing a coagulating agent, and immersing the coagulant in foamed rubber latex to form the outer surface of the cloth glove. After forming a coagulated layer of foamed rubber latex, it is immersed in a rubber latex consisting of 35-65% by weight natural rubber latex and 65-35% by weight isoprene rubber latex to form a solid rubber coating on the outer surface. The present invention provides a method for manufacturing an electrically resistant glove characterized by drying the glove.
前記イソプレンゴムラテックスは、イソプレンモノマー
をアルキルリチウム系,アルキルアルミニウム・四塩化
チタン系,アルキルアルミニウムの代わりにアルミニウ
ムハイドライド誘導体を使用するSNAM系等の重合触
媒で重合したシス1・4構造92〜98%,トランス3
・4構造8〜2%よりなるポリマーのラテックスが使用
される。The isoprene rubber latex has a cis 1.4 structure of 92 to 98%, which is obtained by polymerizing isoprene monomer with a polymerization catalyst such as an alkyl lithium type, an alkyl aluminum/titanium tetrachloride type, or a SNAM type using an aluminum hydride derivative instead of the alkyl aluminum. , transformer 3
- A polymer latex consisting of 8-2% of 4 structures is used.
イソプレンゴムラテフクスには、通常は天然ゴムラテッ
クスに使用される配合剤が用いられる。For isoprene rubber latex, compounding agents normally used for natural rubber latex are used.
しかしながら、化学的安定性が天然ゴムラテックスに較
べていくらか低いため、アニオン系,カチオン系,また
は両性の安定剤が使用される。例えば、アルキルナフタ
リンスルホン酸ソーダ, KOH1アンモニウムカゼ
イン等がよく使用される。However, because the chemical stability is somewhat lower than that of natural rubber latex, anionic, cationic, or amphoteric stabilizers are used. For example, sodium alkylnaphthalene sulfonate, KOH1 ammonium casein, etc. are often used.
天然ゴムラテックスとイソプレンゴムラテソクスとより
なるブレンドゴムラテックスを得るには、先ず、前記安
定剤で所要のゴムラテ・ノクス用配合剤を含んだ配合イ
ソブレンゴムラテックスを安定な状態にしておき、この
配合イソブレンゴムラテックスに、所要のゴムラテック
ス配合剤を含んだ配合天然ゴムラテックスを少量づつ攪
拌しながら、添加していくことが望ましい。この順序を
逆にすると、イソプレンゴムラテックス中の石ケンがと
られ、増粘又はゲル化を起こすことがあるので注意しな
ければならない。In order to obtain a blended rubber latex consisting of natural rubber latex and isoprene rubber latex, first, the compounded isoprene rubber latex containing the required compounding agents for rubber latex is stabilized with the above-mentioned stabilizer. It is desirable to add the compounded natural rubber latex containing the required rubber latex compounding agents little by little to the compounded isobrene rubber latex while stirring. If this order is reversed, the soap in the isoprene rubber latex may be removed, causing thickening or gelation, so care must be taken.
このようにして得られた配合ブレンドゴムラテックスは
例えば他物品の表面に均一に流延し、又は浸漬法等によ
り被覆して適宜の形状に成形し、乾燥し、加硫すること
によってゴム被膜等が得られるが、適正な加硫を得るた
めには、イソプレンゴムラテックス中にはタンパク質,
レシチン,アミノ酸樹脂のような非ゴム成分が含まれな
いので、加硫促進剤,加硫活性剤,老化防止剤等を若干
多く配合する必要がある。加硫剤は硫黄又はテトラメチ
ルチウラム系化合物が使用され、後者は耐熱性が付与さ
れる。The blended rubber latex thus obtained can be uniformly cast onto the surface of other articles, or coated by a dipping method, molded into an appropriate shape, dried, and vulcanized to form a rubber coating. However, in order to obtain proper vulcanization, proteins,
Since it does not contain non-rubber components such as lecithin and amino acid resins, it is necessary to add slightly more vulcanization accelerator, vulcanization activator, anti-aging agent, etc. As the vulcanizing agent, sulfur or a tetramethylthiuram compound is used, and the latter imparts heat resistance.
前記製法を実施することにより、水中でも耐電性がある
ゴム製品が得られるが、更にこの性質を確実にし、又は
向上させるためには、水洗工程を設けなければならない
。By carrying out the above manufacturing method, a rubber product that is electrically resistant even in water can be obtained, but in order to further ensure or improve this property, a water washing step must be provided.
水洗工程により、ラテソクス戒形物中の石ケン,カゼイ
ン等の親水性物質を溶出し、より耐電性を向上させるこ
とができる。By the water washing step, hydrophilic substances such as soap and casein in the latex molten material can be eluted, and the electrical resistance can be further improved.
この水洗工程は、加硫前に行う方法と加硫後に行う方法
とがある。前者の場合がより効率的であるが、威彫物の
形状が複雑な場合は形くずれを起こす虞れがあり、後者
の場合は形くずれを起こす虞はないけれども効率的でな
く、水洗時間が長くなる。This water washing step can be carried out either before vulcanization or after vulcanization. The former case is more efficient, but if the shape of the carved object is complex, there is a risk of it losing its shape, and the latter case, although there is no risk of losing its shape, is not efficient and takes a long time to wash. Become.
従って、戒形物の形状に応じ、何れかの方法が選ばれる
。尚、親水性物質の中にはイソブレンゴムの適正加硫を
若干阻害する物質もあるので、適正加硫を得るという観
点から考慮するならば、後者による方が好ましい。Therefore, one of the methods is selected depending on the shape of the precept. Note that some hydrophilic substances slightly inhibit proper vulcanization of isobrene rubber, so the latter is preferable from the viewpoint of obtaining proper vulcanization.
く実施例〉
交流300V以下の電気回路の作業に使用する電気用低
圧ゴム手袋(以下、「ゴム手袋」という)を製造する場
合について説明する。EXAMPLE> A case will be described in which low-pressure electrical rubber gloves (hereinafter referred to as "rubber gloves") used for working on electrical circuits with an AC voltage of 300 V or less are manufactured.
尚、作業者が電気回路の作業に於いて、着用した手袋が
濡れた状態であっても感電事故から免れるためには、ゴ
ム手袋は後記水中試験で電極間電圧750■での充電電
流(60HZ)が少なくとも10.0mA以下でなけれ
ばならないとされているので、本実施例ではこの数値を
目標とした。In addition, in order to avoid electric shock accidents even if the gloves worn by workers are wet when working on electrical circuits, rubber gloves should be used at a charging current (60 Hz) at an interelectrode voltage of 750 ■ in the underwater test described below. ) must be at least 10.0 mA or less, so this value was targeted in this embodiment.
先ず、第1図に示すように、木製手型(4)に、第2図
に示すような綿糸40番手引揃えのメリヤス編みした手
袋(1)をかぶせた。ここで、第2図の手袋(1)の各
部の寸法(m)は下表の通りであった。First, as shown in FIG. 1, a stockinette-knitted glove (1) of cotton thread count 40 as shown in FIG. 2 was placed over a wooden hand pattern (4). Here, the dimensions (m) of each part of the glove (1) shown in FIG. 2 were as shown in the table below.
1.厚さを除く各部位の寸法は上表を標準とし、許容誤
差は±IOXとする。1. The dimensions of each part, excluding thickness, are based on the table above, and the tolerance is ±IOX.
2.指の太さ(r.J.K.L.M ’)は指の中央部
分で設定する。2. The thickness of the finger (r.J.K.L.M') is set at the center of the finger.
3.※印の寸法は偏平にした時の寸法を示す。3. Dimensions marked with * indicate dimensions when flattened.
この手袋(11を硝酸カルシウムの50%メタノールの
凝固剤溶液に浸漬し、70’cの乾燥室に15分間入れ
て乾燥し、室温に10分間静置後、下記配合の配合天然
ゴムラテックス(ミキサーにて3.5〜4.0倍に泡立
てたもの)中に1分間浸漬し引上げる。This glove (No. 11) was immersed in a coagulant solution of 50% calcium nitrate in methanol, dried by placing it in a 70'c drying chamber for 15 minutes, and left at room temperature for 10 minutes. 3.5 to 4.0 times the foam) for 1 minute and then pulled out.
天然ゴムラテフlyy. (固形分60%) 1
00 重量部fウ5A系加硫剤分散体“ 10
・50X NONOXWSL乳化液0 1
〃ベレックスTA”” 2 〃1
0!’lポニン 水?容液
10 〃本:テトラメチルチウムラジスルフイド
15 〃亜鉛華
15〃
活性化テトラメチルチウムラジスルフイド
5 〃5エチルジチ才カルバミン酸亜鉛
5 〃分敗剤及び水 56
〃
*本:I.C.I(米国)の商品名
o*: 花王一の商品名 シアルキルス11ネコハク酸
ナトリウム布手袋の表面に配合ラテンクスが発泡した状
態で0 . 5 am程度の凝固層(2)を形威してお
り、その上に未凝固の起泡ラテックスがくっついた状態
で引上げられるので、未凝固の起泡ラテソクスを空気で
吹き飛ばしたり、水シャワーで洗い落としたり、或いは
水中に浸漬して除去する。手型(4)に被装した布手袋
(1)は手型によくなじませるため或る程度引張ってい
るので、編目が開いており、少なくとも0.3關〜0.
5 m程度、場所によりそれ以上の寸法の孔がある。普
通の配合ラテックスに浸漬すると水圧により必ず全面に
目洩れして布手袋の裏までラテックスが侵入し、布手袋
の風合を悪くするばかりか、手袋の編目を潰して屈曲抵
抗を増し、柔軟性を失わせるのであるが、本実施例では
、発泡ラテックス凝固層(2)は布手袋(1)の編目に
橋かけした状態で存在し、編目の孔から布手袋の裏まで
侵入した箇所はなかった。発泡ラテソクス凝固N(2)
の厚みは浸漬時間により調節配合ブレンドゴムラテック
スに10秒間2回浸漬し引き上げる。Natural rubber latte lyy. (Solid content 60%) 1
00 Part by weight f 5A vulcanizing agent dispersion" 10
・50X NONOXWSL emulsion 0 1
〃BELEX TA”” 2 〃1
0! 'lponin water? liquid
10 〃Book: Tetramethylthium radical sulfide 15 〃Zinc white
15〃Activated tetramethylthium radical sulfide
5 Zinc carbamate
5 Destroying agent and water 56
〃 *Book: I. C. Product name of I (USA) o*: Product name of Kao Ichi Sialkyrus 11 Sodium cat succinate When the latinx compound is foamed on the surface of the cloth gloves, 0. It forms a coagulated layer (2) with a thickness of about 5 am, and the unsolidified foamed latex is pulled up with it stuck to it, so the unsolidified foamed latex can be blown away with air or washed off with a water shower. or immerse it in water to remove it. The cloth glove (1) covered with the hand pattern (4) is stretched to a certain extent to make it fit well with the hand pattern, so the stitches are open and the stitches are at least 0.3 to 0.3 inches wide.
The holes are approximately 5 m in diameter, with some holes being larger depending on the location. When immersed in ordinary mixed latex, the water pressure causes the latex to leak all over the surface and penetrate into the back of the cloth gloves, not only worsening the feel of the cloth gloves, but also crushing the stitches of the gloves, increasing bending resistance and reducing flexibility. However, in this example, the foamed latex coagulated layer (2) exists in a state that bridges the stitches of the cloth glove (1), and there is no place where the foamed latex coagulated layer (2) penetrates from the hole of the stitch to the back of the cloth glove. Ta. Foamed latex coagulation N (2)
The thickness of the sample is adjusted by adjusting the dipping time.The sample is immersed in the blended rubber latex for 10 seconds twice and pulled up.
Nll
ぬ2
肖3
阻4
ぬ5
チウラム系加硫分敗体
ベレフクス SSL ”
ワックス分散体(固形分50χ)
消泡剤00
水
11 11 11
111
111
0.1 0.1 0.1
27 27 27
本本実施例を理解し易いように固形分に換算して表示し
た.
**花王側製 73キルジフェニルエーテルジスル参ン
酸0リウム*** イ言越化学工業Il@製 商品
名KM71 シリブーンエマルンヨン当初、布手袋に
含有させ・た凝固剤の効力により、発泡ラテックス凝固
層(2)の表面に0.4− 0.5+n厚の固状ゴム被
膜(3)が形威される。Nll Nu2 Port3 Inhibition4 Nu5 Thiuram-based vulcanized decomposer Berefux SSL ” Wax dispersion (solid content 50χ) Antifoaming agent 00 Water 11 11 11 111 111 0.1 0.1 0.1 27 27 27 This book The examples are expressed in terms of solid content to make it easier to understand. ** 73 Kyldiphenyl ether disulfonic acid 0lium manufactured by Kao *** Product name KM71 Silicone Emalun manufactured by Igon-etsu Chemical Industry Il@ Initially, a solid rubber film (3) with a thickness of 0.4-0.5+n is formed on the surface of the foamed latex coagulation layer (2) due to the effect of the coagulant contained in the cloth glove.
若し、凝固剤を補いたいときは、再度、凝固剤溶液に浸
漬,乾燥させて発泡ラテックス凝固層の表面に凝固剤を
付着せしめても良いが、通常は、この工程は不必要であ
る。あと、段階的に100℃まで昇温して乾燥させる。If it is desired to supplement the coagulant, the coagulant may be applied to the surface of the foamed latex coagulated layer by dipping it in the coagulant solution again and drying it, but normally this step is unnecessary. Then, the temperature is raised to 100°C in stages to dry it.
次いで、100℃の間接加硫缶中にて50分間加硫し、
型抜き後、先ずぬ1〜患5配合を用いて、製造した手袋
をなるべく良好な洗條条件例えば75℃の水中にて3時
間洗條し(このような洗條を以下「二次抽出」という)
、その後70℃の乾燥室にて6時間乾燥後、J I S
T8010−1979.4記載の試験装置を用い、
各手袋を2〜6時間水中に浸漬後引上げ、直ちに充電電
流(電極間電圧は交流750V (60Hz)とした)
を測定し、その結果を第1表に示した。次に本発明の所
期の目的に叶った配合と思料されるM3配合を用いて製
造した手袋の二次抽出条件を変えて洗條の影響を調べた
結果を第2表に示した。Next, it was vulcanized for 50 minutes in an indirect vulcanizer at 100°C,
After cutting out the mold, first wash the manufactured gloves using formulations 1 to 5 under the best possible washing conditions, for example, in water at 75°C for 3 hours (such washing is hereinafter referred to as "secondary extraction"). )
After that, after drying in a drying room at 70°C for 6 hours, JIS
Using the test equipment described in T8010-1979.4,
After soaking each glove in water for 2 to 6 hours, it was pulled out and immediately charged with a charging current (the voltage between the electrodes was 750 V AC (60 Hz)).
was measured and the results are shown in Table 1. Next, Table 2 shows the results of examining the influence of washing conditions by changing the secondary extraction conditions for gloves manufactured using the M3 formulation, which is considered to be a formulation that meets the intended purpose of the present invention.
部
1
却
**
×印は本発明の目的にそぐわない結果を得たことを示す
。Part 1 ** × indicates that results not meeting the purpose of the present invention were obtained.
部
2
却
〈発明の効果〉
本発明は手型に被装した布手袋が凝固剤を含有し、これ
を起泡したラテソクス中に浸漬するので、ラテックスは
布手袋の外面に泡構造のまま凝固する。即ち、発泡ゴム
の凝固層が形成される。この凝固層は、1つは、手型を
泡の中に浸漬するので通常の液状ラテックスと異なり水
圧が低いため目洩れせず、2つは、泡構造のラテックス
が孔の中に浸透し難い性質をもっているので目洩れしな
い.かくて、両々相俟って、たとえ0.3〜0.5u程
度の編目の孔があっても、発泡ゴムの凝固層は目洩れし
ないため、布手袋の伸縮性を阻害せず、製品の柔軟性や
作業性が保たれる。同時に凝固層は次いで浸漬されるゴ
ムラテックスの目止めの役割を果たし、固状ゴム被膜の
ピンホール発生の不安をなくするので固状被膜は安全度
をみて必要以上に厚く形成しておく必要はなく、柔軟性
,作業性の向上に寄与する。外層の固状ゴム被膜はラテ
ックス浸漬で作威されるから、薄く形成可能である。加
えて、布手袋と固状ゴム被膜との間に発泡ゴム層がある
ため、固状ゴム被膜の屈曲は構造的に緩衝されて、より
柔軟な感覚のゴム手袋となりうる。更に又、固状ゴム被
膜を35〜65重量%の天然ゴムラテックスと65〜3
5重量%のイソプレンゴムラテ,クスとよりなるブレン
ドゴムラテックスより形或し、そしてその工程中で洗條
さえ充分に行えば、長時間水にさらされた場合であって
も耐電性の低下が少なく、又その上、表面の外観が良好
で柔らかい耐電性ゴムを得ることができる。Part 2 (Effects of the Invention) In the present invention, the cloth glove covered with a hand shape contains a coagulant, and this is immersed in foamed latex, so that the latex coagulates on the outer surface of the cloth glove with a foam structure. do. That is, a solidified layer of foamed rubber is formed. This coagulated layer is created by: (1) the hand mold is immersed in the foam, so unlike normal liquid latex, the water pressure is low, so there is no leakage, and (2) the foam structure of the latex is difficult to penetrate into the pores. Due to its properties, it will not leak. In this way, even if there is a hole in the mesh of about 0.3 to 0.5 u, the coagulated layer of foam rubber will not leak, so it will not impede the elasticity of the cloth glove and will improve the quality of the product. Flexibility and workability are maintained. At the same time, the coagulated layer acts as a seal for the rubber latex that is then dipped, eliminating the fear of pinholes occurring in the solid rubber coating, so it is not necessary to form the solid coating thicker than necessary for safety reasons. This contributes to improved flexibility and workability. Since the outer solid rubber coating is created by dipping in latex, it can be formed thinly. In addition, because of the foam rubber layer between the cloth glove and the solid rubber coating, flexing of the solid rubber coating can be structurally cushioned, resulting in a softer-feeling rubber glove. Furthermore, the solid rubber coating is mixed with 35-65% by weight of natural rubber latex and 65-3% by weight of natural rubber latex.
It is made from a blended rubber latex consisting of 5% by weight of isoprene rubber latex, and as long as it is thoroughly washed during the process, the electrical resistance will not deteriorate even when exposed to water for a long time. Moreover, it is possible to obtain a soft electrically resistant rubber with a good surface appearance.
かかる物性を有する故、本発明は感電防止用電気回路作
業手袋に適用されると効果を充分に発揮しうる。Because of such physical properties, the present invention can fully exhibit its effects when applied to electrical circuit work gloves for preventing electric shock.
第1図は本発明の実施例を示す一部欠切側面図、第2図
は実施例に使用する手袋の平面図を示す。
■・一布手袋,2 一凝固層,3−ゴム被膜,4手型,
A.B.C−M −・−各部の寸法を示す記号。FIG. 1 is a partially cutaway side view showing an embodiment of the present invention, and FIG. 2 is a plan view of a glove used in the embodiment. ■・One cloth glove, 2-coagulated layer, 3-rubber coating, 4-hand type,
A. B. CM - - Symbol indicating the dimensions of each part.
Claims (1)
れを起泡したゴムラテックスに浸漬して布手袋外面に発
泡ゴムラテックスの凝固層を形成した後、35〜65重
量%の天然ゴムラテックスと65〜35重量%のイソプ
レンゴムラテックスとよりなるゴムラテックスに浸漬し
て外面に固状ゴム被膜を形成し、乾燥することを特徴と
する耐電性手袋の製造法。(1) A cloth glove covered with a hand shape is impregnated with a coagulant, and the coagulant is immersed in foamed rubber latex to form a coagulated layer of foamed rubber latex on the outer surface of the cloth glove. A method for producing electrically resistant gloves, which comprises dipping the gloves in a rubber latex consisting of natural rubber latex and 65 to 35% by weight of isoprene rubber latex to form a solid rubber film on the outer surface and drying the gloves.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP30297189A JPH0621364B2 (en) | 1989-11-20 | 1989-11-20 | Manufacturing method of electricity resistant gloves |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP30297189A JPH0621364B2 (en) | 1989-11-20 | 1989-11-20 | Manufacturing method of electricity resistant gloves |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH03161501A true JPH03161501A (en) | 1991-07-11 |
JPH0621364B2 JPH0621364B2 (en) | 1994-03-23 |
Family
ID=17915370
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP30297189A Expired - Fee Related JPH0621364B2 (en) | 1989-11-20 | 1989-11-20 | Manufacturing method of electricity resistant gloves |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0621364B2 (en) |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2001058656A1 (en) * | 2000-02-08 | 2001-08-16 | Ansell Services Inc. | Production of gloves and other articles of flexible polymer material |
JP2002201515A (en) * | 2000-12-27 | 2002-07-19 | Atom Kk | Working glove and method for producing the same |
JP2009057672A (en) * | 2007-08-29 | 2009-03-19 | Techno Tsukihoshi:Kk | Non-conductive glove |
WO2011158696A1 (en) | 2010-06-15 | 2011-12-22 | 株式会社東和コーポレーション | Work glove |
US8894896B2 (en) | 2004-03-31 | 2014-11-25 | A T G Ceylon (Private) Limited | Polymeric garment material |
WO2016099307A1 (en) * | 2014-12-19 | 2016-06-23 | Secura B.C. Sp. Z O.O. | A latex composition for the manufacture of insulation gloves which withstand voltage of 40 v |
JP5945036B1 (en) * | 2015-05-29 | 2016-07-05 | 株式会社東和コーポレーション | Gloves and manufacturing method thereof |
WO2017097991A1 (en) * | 2015-12-10 | 2017-06-15 | G-Zag Ag | Method for producing electrical insulation products made of synthetic polyisoprene (ir) and similar products |
US9890497B2 (en) | 2004-03-31 | 2018-02-13 | A T G Ceylon (Private) Limited | Anti-perspirant glove |
-
1989
- 1989-11-20 JP JP30297189A patent/JPH0621364B2/en not_active Expired - Fee Related
Cited By (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1254002A1 (en) * | 2000-02-08 | 2002-11-06 | Ansell Services Inc. | Production of gloves and other articles of flexible polymer material |
JP2003530236A (en) * | 2000-02-08 | 2003-10-14 | アンセル・ヘルスケア・プロダクツ・インコーポレーテッド | Manufacture of gloves and other articles of flexible polymer material |
AU782156B2 (en) * | 2000-02-08 | 2005-07-07 | Ansell Healthcare Products Llc | Production of gloves and other articles of flexible polymer material |
EP1254002A4 (en) * | 2000-02-08 | 2007-05-23 | Ansell Healthcare Prod Llc | Production of gloves and other articles of flexible polymer material |
WO2001058656A1 (en) * | 2000-02-08 | 2001-08-16 | Ansell Services Inc. | Production of gloves and other articles of flexible polymer material |
US8192834B2 (en) | 2000-02-08 | 2012-06-05 | Ansell Healthcare Products Llc | Production of gloves and other articles of flexible polymer material |
JP2002201515A (en) * | 2000-12-27 | 2002-07-19 | Atom Kk | Working glove and method for producing the same |
JP4638597B2 (en) * | 2000-12-27 | 2011-02-23 | アトム株式会社 | Manufacturing method of work gloves |
US8894896B2 (en) | 2004-03-31 | 2014-11-25 | A T G Ceylon (Private) Limited | Polymeric garment material |
US9890497B2 (en) | 2004-03-31 | 2018-02-13 | A T G Ceylon (Private) Limited | Anti-perspirant glove |
JP2009057672A (en) * | 2007-08-29 | 2009-03-19 | Techno Tsukihoshi:Kk | Non-conductive glove |
WO2011158696A1 (en) | 2010-06-15 | 2011-12-22 | 株式会社東和コーポレーション | Work glove |
US8863317B2 (en) | 2010-06-15 | 2014-10-21 | Towa Corporation Ltd. | Work glove |
WO2016099307A1 (en) * | 2014-12-19 | 2016-06-23 | Secura B.C. Sp. Z O.O. | A latex composition for the manufacture of insulation gloves which withstand voltage of 40 v |
JP5945036B1 (en) * | 2015-05-29 | 2016-07-05 | 株式会社東和コーポレーション | Gloves and manufacturing method thereof |
WO2017097991A1 (en) * | 2015-12-10 | 2017-06-15 | G-Zag Ag | Method for producing electrical insulation products made of synthetic polyisoprene (ir) and similar products |
JP2018538455A (en) * | 2015-12-10 | 2018-12-27 | ジー−ザッグ アーゲー | Method for producing electrical insulation products made of synthetic polyisoprene and similar products |
US11141889B2 (en) | 2015-12-10 | 2021-10-12 | G-Zag Ag | Method for producing electrical insulation products made of synthetic polyisoprene (IR) and similar products |
Also Published As
Publication number | Publication date |
---|---|
JPH0621364B2 (en) | 1994-03-23 |
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