JP2000290816A - Nbr glove - Google Patents
Nbr gloveInfo
- Publication number
- JP2000290816A JP2000290816A JP9825799A JP9825799A JP2000290816A JP 2000290816 A JP2000290816 A JP 2000290816A JP 9825799 A JP9825799 A JP 9825799A JP 9825799 A JP9825799 A JP 9825799A JP 2000290816 A JP2000290816 A JP 2000290816A
- Authority
- JP
- Japan
- Prior art keywords
- glove
- nbr
- weight
- latex
- parts
- 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
- 239000004816 latex Substances 0.000 claims abstract description 45
- 229920000126 latex Polymers 0.000 claims abstract description 45
- 229920001577 copolymer Polymers 0.000 claims abstract description 18
- 239000011347 resin Substances 0.000 claims abstract description 18
- 229920005989 resin Polymers 0.000 claims abstract description 18
- 150000003505 terpenes Chemical class 0.000 claims abstract description 15
- 235000007586 terpenes Nutrition 0.000 claims abstract description 15
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims abstract description 7
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims abstract description 6
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims abstract description 5
- RSWGJHLUYNHPMX-ONCXSQPRSA-N abietic acid Chemical compound C([C@@H]12)CC(C(C)C)=CC1=CC[C@@H]1[C@]2(C)CCC[C@@]1(C)C(O)=O RSWGJHLUYNHPMX-ONCXSQPRSA-N 0.000 claims abstract description 5
- 125000005250 alkyl acrylate group Chemical group 0.000 claims abstract description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 4
- 239000000463 material Substances 0.000 claims description 4
- 229920000459 Nitrile rubber Polymers 0.000 abstract description 52
- 239000002994 raw material Substances 0.000 abstract description 7
- 238000000465 moulding Methods 0.000 abstract 1
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 18
- 238000012360 testing method Methods 0.000 description 18
- 239000000203 mixture Substances 0.000 description 17
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 11
- 239000011593 sulfur Substances 0.000 description 11
- 229910052717 sulfur Inorganic materials 0.000 description 11
- 230000000052 comparative effect Effects 0.000 description 9
- 238000009472 formulation Methods 0.000 description 9
- 238000004073 vulcanization Methods 0.000 description 9
- -1 alkyl acrylate-acrylonitrile- Acrylic acid Chemical compound 0.000 description 8
- KGRVJHAUYBGFFP-UHFFFAOYSA-N 2,2'-Methylenebis(4-methyl-6-tert-butylphenol) Chemical group CC(C)(C)C1=CC(C)=CC(CC=2C(=C(C=C(C)C=2)C(C)(C)C)O)=C1O KGRVJHAUYBGFFP-UHFFFAOYSA-N 0.000 description 7
- PQDCNSONIADPQU-UHFFFAOYSA-N CO.[N+](=O)([O-])[O-].[Ca+2].[N+](=O)([O-])[O-] Chemical compound CO.[N+](=O)([O-])[O-].[Ca+2].[N+](=O)([O-])[O-] PQDCNSONIADPQU-UHFFFAOYSA-N 0.000 description 7
- 150000001875 compounds Chemical class 0.000 description 7
- 238000010438 heat treatment Methods 0.000 description 7
- 239000000049 pigment Substances 0.000 description 7
- 239000011787 zinc oxide Substances 0.000 description 7
- 239000000919 ceramic Substances 0.000 description 6
- 238000013329 compounding Methods 0.000 description 6
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 6
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 5
- 238000001035 drying Methods 0.000 description 5
- 102000020897 Formins Human genes 0.000 description 4
- 108091022623 Formins Proteins 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000005259 measurement Methods 0.000 description 4
- 229920002126 Acrylic acid copolymer Polymers 0.000 description 3
- 244000043261 Hevea brasiliensis Species 0.000 description 3
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 3
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- 229920003052 natural elastomer Polymers 0.000 description 3
- 229920001194 natural rubber Polymers 0.000 description 3
- 239000005011 phenolic resin Substances 0.000 description 3
- 230000000704 physical effect Effects 0.000 description 3
- 239000004014 plasticizer Substances 0.000 description 3
- 229910001220 stainless steel Inorganic materials 0.000 description 3
- 239000010935 stainless steel Substances 0.000 description 3
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- GRWFGVWFFZKLTI-IUCAKERBSA-N (-)-α-pinene Chemical compound CC1=CC[C@@H]2C(C)(C)[C@H]1C2 GRWFGVWFFZKLTI-IUCAKERBSA-N 0.000 description 2
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 238000004364 calculation method Methods 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 229920003145 methacrylic acid copolymer Polymers 0.000 description 2
- 229940117841 methacrylic acid copolymer Drugs 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 229920000915 polyvinyl chloride Polymers 0.000 description 2
- 239000004800 polyvinyl chloride Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- WTARULDDTDQWMU-RKDXNWHRSA-N (+)-β-pinene Chemical compound C1[C@H]2C(C)(C)[C@@H]1CCC2=C WTARULDDTDQWMU-RKDXNWHRSA-N 0.000 description 1
- WTARULDDTDQWMU-IUCAKERBSA-N (-)-Nopinene Natural products C1[C@@H]2C(C)(C)[C@H]1CCC2=C WTARULDDTDQWMU-IUCAKERBSA-N 0.000 description 1
- ZCUMRRFASCPBIH-UHFFFAOYSA-N 2-ethylhexyl prop-2-enoate;prop-2-enenitrile;prop-2-enoic acid Chemical group C=CC#N.OC(=O)C=C.CCCCC(CC)COC(=O)C=C ZCUMRRFASCPBIH-UHFFFAOYSA-N 0.000 description 1
- CFVWNXQPGQOHRJ-UHFFFAOYSA-N 2-methylpropyl prop-2-enoate Chemical compound CC(C)COC(=O)C=C CFVWNXQPGQOHRJ-UHFFFAOYSA-N 0.000 description 1
- BTXXTMOWISPQSJ-UHFFFAOYSA-N 4,4,4-trifluorobutan-2-one Chemical compound CC(=O)CC(F)(F)F BTXXTMOWISPQSJ-UHFFFAOYSA-N 0.000 description 1
- BQACOLQNOUYJCE-FYZZASKESA-N Abietic acid Natural products CC(C)C1=CC2=CC[C@]3(C)[C@](C)(CCC[C@@]3(C)C(=O)O)[C@H]2CC1 BQACOLQNOUYJCE-FYZZASKESA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- 229930185605 Bisphenol Natural products 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- WTARULDDTDQWMU-UHFFFAOYSA-N Pseudopinene Natural products C1C2C(C)(C)C1CCC2=C WTARULDDTDQWMU-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 229920000800 acrylic rubber Polymers 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- XCPQUQHBVVXMRQ-UHFFFAOYSA-N alpha-Fenchene Natural products C1CC2C(=C)CC1C2(C)C XCPQUQHBVVXMRQ-UHFFFAOYSA-N 0.000 description 1
- MVNCAPSFBDBCGF-UHFFFAOYSA-N alpha-pinene Natural products CC1=CCC23C1CC2C3(C)C MVNCAPSFBDBCGF-UHFFFAOYSA-N 0.000 description 1
- 229930006722 beta-pinene Natural products 0.000 description 1
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 1
- QMRMTRCBDHFTIV-UHFFFAOYSA-N butyl prop-2-enoate;prop-2-enenitrile;prop-2-enoic acid Chemical compound C=CC#N.OC(=O)C=C.CCCCOC(=O)C=C QMRMTRCBDHFTIV-UHFFFAOYSA-N 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000007323 disproportionation reaction Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- LCWMKIHBLJLORW-UHFFFAOYSA-N gamma-carene Natural products C1CC(=C)CC2C(C)(C)C21 LCWMKIHBLJLORW-UHFFFAOYSA-N 0.000 description 1
- 239000004519 grease Substances 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 235000001510 limonene Nutrition 0.000 description 1
- 229940087305 limonene Drugs 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 150000002762 monocarboxylic acid derivatives Chemical class 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- KIOWHOMJXAQSMW-UHFFFAOYSA-N phenol;4,6,6-trimethylbicyclo[3.1.1]hept-3-ene Chemical compound OC1=CC=CC=C1.CC1=CCC2C(C)(C)C1C2 KIOWHOMJXAQSMW-UHFFFAOYSA-N 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229910052573 porcelain Inorganic materials 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- GRWFGVWFFZKLTI-UHFFFAOYSA-N rac-alpha-Pinene Natural products CC1=CCC2C(C)(C)C1C2 GRWFGVWFFZKLTI-UHFFFAOYSA-N 0.000 description 1
- 239000012744 reinforcing agent Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
Landscapes
- Moulding By Coating Moulds (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Gloves (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、家庭用や作業用に
適したNBR製手袋に関し、詳細には、手袋として充分
な皮膜強度を備え、柔軟で屈曲性に富み、なお且つ装着
作業時に手袋表面での滑りが著しく改善されたNBR製
手袋に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to gloves made of NBR suitable for home use and work, and more particularly, to gloves having a sufficient film strength as a glove, being flexible and flexible, and capable of being worn when worn. The present invention relates to an NBR glove having significantly improved surface slippage.
【0002】[0002]
【従来の技術】NBR(アクリロニトリルブタジエンゴ
ム:Acryronitrile butadiene rubber)を素材とする手
袋は、NR(天然ゴム:Natural rubber)やPVC(ポ
リ塩化ビニル:Polyvinylchloride)を素材とする手袋
に比べ耐油性、耐突き差し性、耐摩耗性などに優れた性
質を持っている。その反面、NBRを素材とする手袋
は、NRに比べると非常に反発弾性が劣り柔軟性を欠
き、物を掴んだときに手袋表面で滑り易いと言う欠点が
指摘され、作業の安全性の点から問題視されることが多
かった。この欠点を改善するため、従来は加硫剤配合の
調整、または軟化剤の添加にて柔軟化する試みがなされ
ていた。2. Description of the Related Art Gloves made of NBR (acrylonitrile butadiene rubber) are more oil- and grease-resistant than gloves made of NR (natural rubber) and PVC (polyvinylchloride). It has excellent properties such as piercing and abrasion resistance. On the other hand, gloves made of NBR have a drawback that they have extremely low rebound resilience and lack flexibility compared to NR, and they are slippery on the glove surface when grasping an object. Was often viewed as a problem. In order to remedy this drawback, attempts have conventionally been made to soften the composition by adjusting the blending of a vulcanizing agent or by adding a softener.
【0003】[0003]
【発明が解決しようとする課題】ところで、加硫剤配合
の調整では、NBRの加硫剤として多種の薬剤が提供さ
れているが、主に硫黄(S)、酸化亜鉛(ZnO)の併
用が一般的であり、加硫形成するNBR皮膜の強度およ
び柔軟性は硫黄(S)および酸化亜鉛(ZnO)の配合
部数によって大きく影響される。家庭用や作業用のNB
R製手袋に配合される加硫系は、硫黄(S)および酸化
亜鉛(ZnO)の合計配合量が通常2〜5重量部の範囲
で使用されることが多く、皮膜の引張強度は強靭である
が、一般的に柔軟性が小さく、殊に低温域(0℃付近)
では硬い。In the preparation of vulcanizing agents, various agents are provided as vulcanizing agents for NBR. However, sulfur (S) and zinc oxide (ZnO) are mainly used in combination. Generally, the strength and flexibility of an NBR film formed by vulcanization are greatly affected by the number of parts of sulfur (S) and zinc oxide (ZnO). NB for home and work
In the vulcanization system blended in R gloves, the total blended amount of sulfur (S) and zinc oxide (ZnO) is often used in the range of usually 2 to 5 parts by weight, and the tensile strength of the film is strong. Yes, but generally low flexibility, especially in low temperature range (around 0 ° C)
Then it is hard.
【0004】このため、本発明者らは研究を重ねること
によって、柔軟性と手袋表面の滑り性はいずれも手袋皮
膜の物性に係わるものであり、滑り性は物を掴んだとき
の手袋表面皮膜と物表面との接触面積がより大きくなる
こと、すなわち手袋表面皮膜の柔らかさが大きく関係す
ることを実証してきた。その中で、硫黄(S)および酸
化亜鉛(ZnO)の合計配合量を1〜2重量部の範囲で
使用し、100%モジュラス値を20kg/cm2以下
に設定して滑り防止効果を向上させようとしたが、この
方法のみでは手袋皮膜としての充分な強度が得られにく
い欠点があった。[0004] Therefore, the inventors of the present invention have repeatedly studied and found that both the flexibility and the slipperiness of the glove surface are related to the physical properties of the glove film, and the slipperiness is determined by the glove surface film when the object is gripped. It has been demonstrated that the contact area between the glove and the object surface becomes larger, that is, the softness of the glove surface film is greatly related. Among them, the total blending amount of sulfur (S) and zinc oxide (ZnO) is used in the range of 1 to 2 parts by weight, and the 100% modulus value is set to 20 kg / cm 2 or less to improve the slip prevention effect. However, this method alone has a disadvantage that it is difficult to obtain sufficient strength as a glove film.
【0005】また、軟化剤としては、アジピン酸エステ
ル系の可塑剤、鉱物油、植物油などがよく使用されてい
るが、これらは、少量添加で柔軟化に大きく貢献する
が、次第に手袋表面に移行してき、水漏れの状況での作
業では非常に滑りやすくなるという問題があった。本発
明はこのような課題を解決するもので、成形皮膜が柔ら
かく、皮膜表面の滑り性が少なく、実用に耐え得る皮膜
強度を持ったNBR製手袋を提供することを目的とする
ものである。As the softener, adipate-based plasticizers, mineral oils, vegetable oils, and the like are often used. These additives greatly contribute to softening when added in small amounts, but gradually migrate to the glove surface. Then, there was a problem that it became very slippery when working in a water leak situation. An object of the present invention is to solve such a problem, and an object of the present invention is to provide an NBR glove having a soft formed film, low slipperiness on the film surface, and a film strength enough to withstand practical use.
【0006】[0006]
【発明を解決するための手段】本発明者らは、家庭用、
作業用NBR製手袋として充分に実用できるだけの皮膜
強度と柔軟性を兼ね備え、掴んだときの手袋表面の滑り
を防止することを同時に保持させる技術の開発について
鋭意研究を重ねた。そして、アクリレート系共重合ラテ
ックスにおいてモノマーの種類と割合を選定し開発を進
めた結果、アルキルアクリレート−アクリロニトリル−
アクリル酸またはメタクリル酸共重合ラテックスをNB
Rラテックスにブレンドするとその皮膜は柔軟性に富
み、水漏れ時にも滑りがほとんどないこと、またロジン
系樹脂ラテックスとテルペン系樹脂ラテックスの一方も
しくは両方をNBRラテックス固形分に対して1〜10
重量部添加すると強度低下が緩和され、実用性の基準と
した200kg/cm2以上の引張強度を維持できるこ
とを見出し、本発明を完成した。SUMMARY OF THE INVENTION The present inventors have found that
The intense research has been conducted on the development of a technique which has both film strength and flexibility enough to be practically used as a working NBR glove, and simultaneously prevents the glove surface from slipping when gripped. Then, as a result of selecting the type and ratio of the monomer in the acrylate-based copolymer latex and proceeding with the development, an alkyl acrylate-acrylonitrile-
Acrylic acid or methacrylic acid copolymer latex
When blended with R latex, the film is rich in flexibility and hardly slips when water leaks, and one or both of a rosin-based resin latex and a terpene-based resin latex is 1 to 10 times the solid content of NBR latex.
The addition of parts by weight alleviates the decrease in strength, and has found that a tensile strength of 200 kg / cm 2 or more, which is the standard of practicality, can be maintained, and the present invention has been completed.
【0007】すなわち本発明のNBR製手袋は、アルキ
ルアクリレートとアクリロニトリルとアクリル酸または
メタクリル酸との共重合体と、ロジン酸樹脂またはテル
ペン系樹脂の少なくとも一方とを配合したNBRラテッ
クスを材料に用いて成形されてなることを特徴とするも
のである。ここで、ロジン系樹脂ラテックス、テルペン
系樹脂ラテックスは、異種ラテックスブレンドにおいて
優れた相溶化剤となり、100%モジュラスを上げるこ
となく、すなわちNBR皮膜を硬化させることなく、引
張強度を強化する補助強化剤として重要な働きをする。That is, the glove made of NBR of the present invention uses an NBR latex blended with a copolymer of an alkyl acrylate, acrylonitrile, acrylic acid or methacrylic acid, and at least one of a rosin acid resin and a terpene resin. It is characterized by being formed. Here, the rosin-based resin latex and the terpene-based resin latex are excellent compatibilizers in different types of latex blends, and are auxiliary reinforcing agents that enhance the tensile strength without increasing the modulus by 100%, that is, without curing the NBR film. As an important function.
【0008】本発明に用いられるNBRラテックスは、
いわゆる低〜高アクリロニトリルNBRと呼ばれるもの
で、アクリロニトリルを20〜45モル%含有し、10
%以下のカルボキシル変性基を持つものであり、手袋材
料として一般に使用されている範囲の分子量のものを使
用可能である。ロジン系樹脂は、アビエチン酸を主成分
とするモノカルボン酸であるロジン酸をマレイン酸また
はフマール酸で変性させた樹脂酸、あるいはそれらを不
均化または水素添加などで安定化を図った後、各種のポ
リアルコールと反応させてエステル化し、乳化剤の存在
下でエマルジョン化したものが使われる。The NBR latex used in the present invention comprises:
A so-called low to high acrylonitrile NBR containing 20 to 45 mol% of acrylonitrile,
% Or less of a carboxyl-modified group, and those having a molecular weight in a range generally used as a glove material can be used. Rosin resin is a resin acid obtained by modifying rosin acid, which is a monocarboxylic acid containing abietic acid as a main component, with maleic acid or fumaric acid, or after stabilizing them by disproportionation or hydrogenation, What is esterified by reacting with various polyalcohols and emulsified in the presence of an emulsifier is used.
【0009】テルペン系樹脂には、テルペン樹脂、テル
ペンフェノール樹脂があり、テルペン樹脂としては、主
としてα−ピネン、β−ピネン、ジペンテン(リモネ
ン)の3種類のテルペンを単独または、共重合したも
の、さらにテルペン樹脂に各種のフェノールを重合させ
たα−ピネンフェノール樹脂、ジペンテンフェノール樹
脂、テルペンビスフェノール樹脂などを使用できる。Terpene resins include terpene resins and terpene phenol resins. The terpene resins are mainly terpenes of α-pinene, β-pinene, and dipentene (limonene), which are used alone or copolymerized. Further, α-pinene phenol resin, dipentene phenol resin, terpene bisphenol resin, etc. obtained by polymerizing various phenols on terpene resin can be used.
【0010】アルキルアクリレート成分としては、エチ
ルアクリレート、n−ブチルアクリレート、iso−ブ
チルアクリレート、t−ブチルアクリレート、2−エチ
ルヘキシルアクリレートなどが有効である。アルキルア
クリレート−アクリロニトリル−アクリル酸またはメタ
クリル酸の共重合体のモノマーの組成比は、アルキルア
クリレート;94〜75モル(%)、アクリロニトリ
ル;5〜20モル(%)、アクリル酸またはメタクリル
酸;1〜5モル(%)が好適であり、ブレンドするNB
Rラテックスの特性に合わせて適切な割合で重合したア
ルキルアクリレート共重合物が供される。共重合体の分
子量には特に限定はない。As the alkyl acrylate component, ethyl acrylate, n-butyl acrylate, iso-butyl acrylate, t-butyl acrylate, 2-ethylhexyl acrylate and the like are effective. The composition ratio of the monomer of the copolymer of alkyl acrylate-acrylonitrile-acrylic acid or methacrylic acid is as follows: alkyl acrylate; 94 to 75 mol (%), acrylonitrile; 5 to 20 mol (%), acrylic acid or methacrylic acid; 5 mol (%) is preferred and the NB to be blended
An alkyl acrylate copolymer polymerized in an appropriate ratio according to the properties of the R latex is provided. There is no particular limitation on the molecular weight of the copolymer.
【0011】NBR製手袋の製造に際しては、上記した
成分を配合したNBRラテックスを材料として浸漬加工
法または塗布加工法が行われる。In the production of gloves made of NBR, a dipping process or a coating process is performed using NBR latex containing the above-mentioned components as a material.
【0012】[0012]
【発明の実施の形態】以下、本発明を実施の形態に基づ
いて説明するが、本発明はこれらに限定されるものでは
ない。 実施の形態1 陶磁器製手袋型を30%硝酸カルシウムのメタノール溶
液に浸漬したのち、下記配合(1)のNBRラテックス
コンパウンドに30秒間漬け、引き上げて80℃×20
minで乾燥させた後、130℃×1hrで加熱処理を
して手型より反転離型してNBR製手袋を試作した。こ
の手袋の掌部から試験片(63.5mm×63.5m
m)を切り取り、ウェット条件での動摩擦係数を測定、
算出した。また、この手袋の引張強度および100%モ
ジュラスを手袋裾部より切り取った試験片で測定、算出
した。この結果データーを表1に示す。ただし、配合原
料中のNBRラテックスは Nippol LX550(日本ゼオン
株式会社製;以下同じ)であり、nBA−AN−AA共
重合ラテックスはn−ブチルアクリレート;88モル%
−アクリロニトリル;10モル%−アクリル酸;2モル
%の共重合体ラテックスであって、分子量約20万のも
のであり、ともに固形分重量で示す。DESCRIPTION OF THE PREFERRED EMBODIMENTS Hereinafter, the present invention will be described based on embodiments, but the present invention is not limited to these. Embodiment 1 A ceramic glove mold was immersed in a 30% calcium nitrate methanol solution, then immersed in an NBR latex compound having the following composition (1) for 30 seconds, pulled up, and pulled up to 80 ° C. × 20.
After drying for min, heat treatment was performed at 130 ° C. × 1 hr, and the mold was inverted and released from a hand mold to produce a prototype NBR glove. A test piece (63.5 mm x 63.5 m) was taken from the palm of this glove.
m), measure the dynamic friction coefficient under wet conditions,
Calculated. The tensile strength and 100% modulus of this glove were measured and calculated using a test piece cut from the glove hem. Table 1 shows the result data. However, the NBR latex in the compounding raw material is Nippol LX550 (manufactured by Nippon Zeon Co., Ltd .; the same applies hereinafter), and the nBA-AN-AA copolymer latex is n-butyl acrylate; 88 mol%
Acrylonitrile; 10 mol% -acrylic acid; 2 mol% copolymer latex having a molecular weight of about 200,000, both of which are indicated by solids weight.
【0013】 配合(1) NBRラテックス 70重量部 nBA−AN−AA共重合ラテックス 30重量部 酸化亜鉛 2重量部 硫黄 1重量部 加硫促進剤 0.5重量部 老化防止剤 1重量部 顔料 適量 変性ロジン酸エステル 5重量部 実施の形態2 陶磁器製手袋型を30%硝酸カルシウムのメタノール溶
液に浸漬したのち、下記配合(2)のNBRラテックス
コンパウンドに30秒間漬け、引き上げて80℃×20
minで乾燥させた後、130℃×1hrで加熱処理を
して手型より反転離型してNBR製手袋を試作した。こ
の手袋の掌部から試験片(63.5mm×63.5m
m)を切り取り、ウェット条件での動摩擦係数を測定、
算出した。また、この手袋の引張強度および100%モ
ジュラスを手袋裾部より切り取った試験片で測定、算出
した。この結果データーを表1に示す。Formulation (1) NBR latex 70 parts by weight nBA-AN-AA copolymer latex 30 parts by weight Zinc oxide 2 parts by weight Sulfur 1 part by weight Vulcanization accelerator 0.5 part by weight Antioxidant 1 part by weight Pigment appropriate amount modification Rosin acid ester 5 parts by weight Embodiment 2 A ceramic glove mold is immersed in a 30% calcium nitrate methanol solution, then immersed in an NBR latex compound of the following formulation (2) for 30 seconds, pulled up, and pulled up to 80 ° C. × 20.
After drying for min, heat treatment was performed at 130 ° C. × 1 hr, and the mold was inverted and released from a hand mold to produce a prototype NBR glove. A test piece (63.5 mm x 63.5 m) was taken from the palm of this glove.
m), measure the dynamic friction coefficient under wet conditions,
Calculated. The tensile strength and 100% modulus of this glove were measured and calculated using a test piece cut from the glove hem. Table 1 shows the result data.
【0014】 配合(2) NBRラテックス 70重量部 nBA−AN−AA共重合ラテックス 30重量部 酸化亜鉛 2重量部 硫黄 1重量部 加硫促進剤 0.5重量部 老化防止剤 1重量部 顔料 適量 テルペンフェノール 5重量部 実施の形態3 陶磁器製手袋型を30%硝酸カルシウムのメタノール溶
液に浸漬したのち、下記配合(3)のNBRラテックス
コンパウンドに30秒間漬け、引き上げて80℃×20
minで乾燥させた後、130℃×1hrで加熱処理を
して手型より反転離型してNBR製手袋を試作した。こ
の手袋の掌部から試験片(63.5mm×63.5m
m)を切り取り、ウェット条件での動摩擦係数を測定、
算出した。また、またこの手袋の引張強度および100
%モジュラスを手袋裾部より切り取った試験片で測定、
算出した。この結果データーを表1に示す。ただし、配
合原料中の2EHA−AN−AA共重合ラテックスとは
2エチルヘキシルアクリレート;88モル%−アクリロ
ニトリル;10モル%−アクリル酸;2モル%の共重合
体ラテックスであって、分子量約20万である。Formulation (2) NBR latex 70 parts by weight nBA-AN-AA copolymer latex 30 parts by weight Zinc oxide 2 parts by weight Sulfur 1 part by weight Vulcanization accelerator 0.5 part by weight Antioxidant 1 part by weight Pigment appropriate amount Terpene Phenol 5 parts by weight Embodiment 3 A ceramic glove mold was immersed in a 30% calcium nitrate methanol solution, then immersed in an NBR latex compound having the following composition (3) for 30 seconds, pulled up, and pulled up to 80 ° C. × 20.
After drying for min, heat treatment was performed at 130 ° C. × 1 hr, and the mold was inverted and released from a hand mold to produce a prototype NBR glove. A test piece (63.5 mm x 63.5 m) was taken from the palm of this glove.
m), measure the dynamic friction coefficient under wet conditions,
Calculated. Also, the glove's tensile strength and 100 g
% Modulus measured on a test piece cut from the glove hem,
Calculated. Table 1 shows the result data. However, the 2EHA-AN-AA copolymer latex in the compounding raw material is a copolymer latex of 2-ethylhexyl acrylate; 88 mol% -acrylonitrile; 10 mol% -acrylic acid; 2 mol%, and has a molecular weight of about 200,000. is there.
【0015】 配合(3) NBRラテックス 70重量部 2EHA−AN−AA共重合ラテックス 30重量部 酸化亜鉛 2重量部 硫黄 1重量部 加硫促進剤 0.5重量部 老化防止剤 1重量部 顔料 適量 変性ロジン酸エステル 5重量部 実施の形態4 陶磁器製手袋型を30%硝酸カルシウムのメタノール溶
液に浸漬したのち、下記配合(4)のNBRラテックス
コンパウンドに30秒間漬け、引き上げて80℃×20
minで乾燥させた後、130℃×1hrで加熱処理を
して手型より反転離型してNBR製手袋を試作した。こ
の手袋の掌部から試験片(63.5mm×63.5m
m)を切り取り、ウェット条件での動摩擦係数を測定、
算出した。また、NBR製手袋の引張強度および100
%モジュラスを手袋裾部より切り取った試験片で測定、
算出した。この結果データーを表1に示す。ただし、配
合原料品のnBA−AN−MA共重合ラテックスとはn
−ブチルアクリレート;88モル%−アクリロニトリ
ル;10モル%−メタクリル酸;2モル%の共重合体ラ
テックスであって、分子量約20万である。Formulation (3) NBR latex 70 parts by weight 2EHA-AN-AA copolymer latex 30 parts by weight Zinc oxide 2 parts by weight Sulfur 1 part by weight Vulcanization accelerator 0.5 part by weight Antioxidant 1 part by weight Pigment appropriate amount modification Rosin acid ester 5 parts by weight Embodiment 4 A ceramic glove mold is immersed in a 30% calcium nitrate methanol solution, then immersed in an NBR latex compound of the following formulation (4) for 30 seconds, pulled up, and pulled up to 80 ° C. × 20.
After drying for min, heat treatment was performed at 130 ° C. × 1 hr, and the mold was inverted and released from a hand mold to produce a prototype NBR glove. A test piece (63.5 mm x 63.5 m) was taken from the palm of this glove.
m), measure the dynamic friction coefficient under wet conditions,
Calculated. In addition, the tensile strength of gloves made of NBR and 100
% Modulus measured on a test piece cut from the glove hem,
Calculated. Table 1 shows the result data. However, nBA-AN-MA copolymer latex of the compounding raw material is n
Butyl acrylate; 88 mol% -acrylonitrile; 10 mol% -methacrylic acid; 2 mol% copolymer latex having a molecular weight of about 200,000.
【0016】 配合(4) NBRラテックス 70重量部 nBA−AN−MA共重合ラテックス 30重量部 酸化亜鉛 2重量部 硫黄 1重量部 加硫促進剤 0.5重量部 老化防止剤 1重量部 顔料 適量 変性ロジン酸エステル 5重量部 比較例1 実施の形態1と同様に、陶磁器製手袋型を30%硝酸カ
ルシウムのメタノール溶液に浸漬したのち、下記配合
(5)のNBRラテックスコンパウンドに30秒間漬
け、引き上げて80℃×20minで乾燥させた後、1
30℃×1hrで加熱処理をして手型より反転離型して
NBR製手袋を試作した。この手袋の掌部から試験片
(63.5mm×63.5mm)を切り取り、ウェット
条件での動摩擦係数を測定、算出した。また、NBR製
手袋の引張強度および100%モジュラスを手袋裾部よ
り切り取った試験片で測定、算出した。この結果データ
ーを表1に示す。Formulation (4) NBR latex 70 parts by weight nBA-AN-MA copolymer latex 30 parts by weight Zinc oxide 2 parts by weight Sulfur 1 part by weight Vulcanization accelerator 0.5 part by weight Antioxidant 1 part by weight Pigment appropriate amount modification 5% by weight of rosin acid ester Comparative Example 1 As in Embodiment 1, a ceramic glove mold was immersed in a 30% calcium nitrate methanol solution, then immersed in an NBR latex compound having the following composition (5) for 30 seconds, and pulled up. After drying at 80 ° C x 20 min, 1
A heat treatment was performed at 30 ° C. × 1 hr, and the mold was inverted and released from the hand mold to produce a prototype NBR glove. A test piece (63.5 mm × 63.5 mm) was cut out from the palm of this glove, and the dynamic friction coefficient under wet conditions was measured and calculated. Further, the tensile strength and the 100% modulus of the NBR glove were measured and calculated using a test piece cut from the glove hem. Table 1 shows the result data.
【0017】 配合(5) NBRラテックス 70重量部 nBA−AN−AA共重合ラテックス 30重量部 酸化亜鉛 2重量部 硫黄 1重量部 加硫促進剤 0.5重量部 老化防止剤 1重量部 顔料 適量 比較例2 実施の形態1と同様に、陶磁器製手袋型を30%硝酸カ
ルシウムのメタノール溶液に浸漬したのち、下記配合
(6)のNBRラテックスコンパウンドに30秒間漬
け、引き上げて80℃×20minで乾燥させた後、1
30℃×1hrで加熱処理をして手型より反転離型して
NBR製手袋を試作した。この手袋の掌部から試験片
(63.5mm×63.5mm)を切り取り、ウェット
条件での動摩擦係数を測定、算出した。また、NBR製
手袋の引張強度および100%モジュラスを手袋裾部よ
り切り取った試験片で測定、算出した。この結果データ
ーを表1に示す。Formulation (5) NBR latex 70 parts by weight nBA-AN-AA copolymer latex 30 parts by weight Zinc oxide 2 parts by weight Sulfur 1 part by weight Vulcanization accelerator 0.5 part by weight Antioxidant 1 part by weight Pigment appropriate amount comparison Example 2 As in Embodiment 1, a ceramic glove mold was immersed in a 30% calcium nitrate methanol solution, then immersed in an NBR latex compound having the following composition (6) for 30 seconds, pulled up and dried at 80 ° C. × 20 min. After one
A heat treatment was performed at 30 ° C. × 1 hr, and the mold was inverted and released from the hand mold to produce a prototype NBR glove. A test piece (63.5 mm × 63.5 mm) was cut out from the palm of this glove, and the dynamic friction coefficient under wet conditions was measured and calculated. Further, the tensile strength and the 100% modulus of the NBR glove were measured and calculated using a test piece cut from the glove hem. Table 1 shows the result data.
【0018】 配合(6) NBRラテックス 100重量部 酸化亜鉛 2重量部 硫黄 1重量部 加硫促進剤 0.5重量部 老化防止剤 1重量部 顔料 適量 比較例3 実施の形態1と同様に、陶磁器製手袋型を30%硝酸カ
ルシウムのメタノール溶液に浸漬したのち、下記配合
(7)のNBRラテックスコンパウンドに30秒間漬
け、引き上げて80℃×20minで乾燥させた後、1
30℃×1hrで加熱処理をして手型より反転離型して
NBR製手袋を試作した。この手袋の掌部から試験片
(63.5mm×63.5mm)を切り取り、ウェット
条件での動摩擦係数を測定、算出した。また、NBR製
手袋の引張強度および100%モジュラスを手袋裾部よ
り切り取った試験片で測定、算出した。この結果データ
ーを表1に示す。Formulation (6) NBR latex 100 parts by weight Zinc oxide 2 parts by weight Sulfur 1 part by weight Vulcanization accelerator 0.5 part by weight Antioxidant 1 part by weight Pigment suitable amount Comparative Example 3 As in the first embodiment, porcelain After the glove mold was dipped in a 30% calcium nitrate methanol solution, it was dipped in an NBR latex compound having the following composition (7) for 30 seconds, pulled up and dried at 80 ° C. for 20 minutes.
A heat treatment was performed at 30 ° C. × 1 hr, and the mold was inverted and released from the hand mold to produce a prototype NBR glove. A test piece (63.5 mm × 63.5 mm) was cut out from the palm of this glove, and the dynamic friction coefficient under wet conditions was measured and calculated. Further, the tensile strength and the 100% modulus of the NBR glove were measured and calculated using a test piece cut from the glove hem. Table 1 shows the result data.
【0019】 配合(7) NBRラテックス 100重量部 アジピン酸エステル系可塑剤 10重量部 酸化亜鉛 2重量部 硫黄 1重量部 加硫促進剤 0.5重量部 老化防止剤 1重量部 顔料 適量 上記した実施の形態1〜4および比較例1〜3における
測定、算出、およびそれに基く評価は以下のようにして
行なった。 動摩擦係数の測定、算出 摩擦係数測定装置にてASTM D 1894に基づ
き、移動重錘に手袋掌から切り取ったNBRフィルム試
験片を取り付け、水を一定量張ったステンレス板上を1
50mm/minで移動距離130mm走行させ、試験
片とステンレス板との摩擦によって変化する荷重を測定
し、走行抵抗(動摩擦係数)を算出した。Formulation (7) NBR latex 100 parts by weight Adipate ester plasticizer 10 parts by weight Zinc oxide 2 parts by weight Sulfur 1 part by weight Vulcanization accelerator 0.5 part by weight Antioxidant 1 part by weight Pigment appropriate amount Measurements, calculations, and evaluations based on the forms 1-4 and Comparative Examples 1-3 were performed as follows. Measurement and Calculation of Dynamic Friction Coefficient Based on ASTM D 1894, an NBR film test piece cut from the glove palm was attached to a moving weight using a friction coefficient measurement device, and a stainless steel plate with a fixed amount of water was placed on a moving stainless steel plate.
The test piece was run at a moving distance of 130 mm at a speed of 50 mm / min, a load that changed due to friction between the test piece and the stainless steel plate was measured, and a running resistance (dynamic friction coefficient) was calculated.
【0020】 移動重錘の接触面積 63.5mm×63.5mm 計算式 μK(動摩擦係数)=C/D C=均斉な走行になってからの平均荷重値(g) D=移動重錘の重量 200g 引張強度、100%モジュラスの測定 NBR製手袋の平滑部から試験片(63.5mm×6
3.5mm)を4枚切り抜き、引張強度および100%
モジュラスをJIS K 6301に準拠して測定し
た。 滑り防止の評価 動摩擦係数の値が大きいほど滑り止め効果があるとし
た。 軟らかさの評価 100%モジュラスが低いほど柔軟であるとした。Contact Area of Moving Weight 63.5 mm × 63.5 mm Formula μK (Coefficient of Dynamic Friction) = C / D C = Average Load Value (g) after Uniform Running D = Weight of Moving Weight 200 g Measurement of tensile strength and 100% modulus A test piece (63.5 mm × 6
3.5mm), cut out 4 pieces, tensile strength and 100%
The modulus was measured according to JIS K6301. Evaluation of anti-slip It was determined that the larger the value of the coefficient of dynamic friction, the more effective the anti-slip effect. Evaluation of softness The lower the 100% modulus, the more flexible.
【0021】[0021]
【表1】 比較例2が一般に家庭用、作業用手袋として実用されて
いる従来のNBR製手袋の物性であり、引張強度が42
0kg/cm2と強靭であるが、100%モジュラスが
28.0kg/cm2と硬い。比較例1はNBRラテッ
クスにnBA−AN−AA(nBA/AN/AA=88
モル%/10モル%/2モル%)共重合ラテックスをブ
レンドした手袋の物性を備えているが、100%モジュ
ラスが20kg/cm2以下になると引張強度が170
kg/cm2まで下がり実用強度の基準とした200k
g/cm2を下回ってしまう。【table 1】 Comparative Example 2 shows the physical properties of a conventional NBR glove generally used as a household or work glove, and the tensile strength was 42%.
Although it is as tough as 0 kg / cm 2 , it has a 100% modulus as hard as 28.0 kg / cm 2 . In Comparative Example 1, nBA-AN-AA (nBA / AN / AA = 88) was added to the NBR latex.
(Mol% / 10 mol% / 2 mol%) The gloves blended with the copolymerized latex have the physical properties, but when the 100% modulus becomes 20 kg / cm 2 or less, the tensile strength becomes 170.
200k as the standard for practical strength, down to kg / cm 2
g / cm 2 .
【0022】一方、実施の形態1は比較例1に比べて変
性ロジン酸エステルを5重量部添加したものであるが、
100%モジュラスが18.0kg/cm2と柔軟性を
保ちながら、引張強度が222kg/cm2と約30%
も強化されている。実施の形態2は、実施の形態1の配
合原料中の変性ロジン酸エステルの代わりにテルペンフ
ェノールを5重量部添加したものであるが、100%モ
ジュラスが18.3kg/cm2と柔軟であり、引張強
度は235kg/cm2と、比較例1に比べて約40%
も強化されている。On the other hand, in the first embodiment, the modified rosin acid ester was added in an amount of 5 parts by weight as compared with the comparative example 1.
The tensile strength is 222 kg / cm 2 and about 30% while maintaining the flexibility at 100% modulus of 18.0 kg / cm 2.
Has also been enhanced. In the second embodiment, terpene phenol is added in an amount of 5 parts by weight instead of the modified rosin acid ester in the compounding raw material of the first embodiment, but the 100% modulus is as flexible as 18.3 kg / cm 2 , The tensile strength is 235 kg / cm 2 , about 40% as compared with Comparative Example 1.
Has also been enhanced.
【0023】実施の形態3は、実施の形態1の配合原料
中のn−ブチルアクリレート−アクリロニトリル−アク
リル酸共重合体を2エチルヘキシルアクリレート−アク
リロニトリル−アクリル酸共重合体に代えたものであ
り、実施の形態4は、実施の形態1の配合原料中のn−
ブチルアクリレート−アクリロニトリル−アクリル酸共
重合体をn−ブチルアクリレート−アクリロニトリル−
メタクリル酸共重合体に代えたものであるが、両方とも
100%モジュラスが20kg/cm2以下と柔軟であ
り、引張強度も200kg/cm2以上に強化されてい
る。In the third embodiment, the n-butyl acrylate-acrylonitrile-acrylic acid copolymer in the compounding raw material of the first embodiment is replaced with a 2-ethylhexyl acrylate-acrylonitrile-acrylic acid copolymer. In the embodiment 4, n- in the compounding raw material of the embodiment 1
Butyl acrylate-acrylonitrile-acrylic acid copolymer was converted to n-butyl acrylate-acrylonitrile-
In place of the methacrylic acid copolymer, both are flexible with a 100% modulus of 20 kg / cm 2 or less, and have a reinforced tensile strength of 200 kg / cm 2 or more.
【0024】柔軟性にともなう滑り止め効果の点では、
実施の形態1〜4および比較例1〜2において、低モジ
ュラスなもの程、滑り止め効果があることがわかる。可
塑剤を添加した比較例3では動摩擦係数μKは0.17
であり、滑り止め効果が著しく劣ることを示している。In terms of the anti-slip effect associated with flexibility,
In Embodiments 1 to 4 and Comparative Examples 1 and 2, it can be seen that the lower the modulus, the more effective it is in preventing slippage. In Comparative Example 3 in which a plasticizer was added, the dynamic friction coefficient μK was 0.17
Which indicates that the anti-slip effect is remarkably inferior.
【0025】[0025]
【発明の効果】以上のように本発明によれば、NBRラ
テックスとアルキルアクリレート−アクリロニトリル−
アクリル酸またはメタクリル酸の共重合ラテックスとロ
ジン酸系樹脂またはテルペン系樹脂とを適量配合するこ
とにより、NBR製手袋に、家庭用または作業用として
充分に耐久性のある皮膜強度を持たせることができ、な
お且つ柔軟で物を掴むときにおいても手袋表面での滑り
を起こすことなく快適な作業ができるようになる。As described above, according to the present invention, the NBR latex and the alkyl acrylate-acrylonitrile-
By mixing an appropriate amount of a copolymer latex of acrylic acid or methacrylic acid and a rosin acid resin or a terpene resin, it is possible to give an NBR glove a sufficiently durable film strength for home use or work use. It is possible to work comfortably without slipping on the surface of the glove even when gripping an object.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.7 識別記号 FI テーマコート゛(参考) C08L 33/20 C08L 33/20 93/00 93/00 93/04 93/04 // B29K 9:00 33:00 86:00 B29L 31:48 Fターム(参考) 3B033 AB10 AC03 BA01 4F205 AA20E AA21E AA46 AA49 AC05 AH70 GA08 GB01 GC01 GF01 GW06 4J002 AC07W AF02Y BA00Y BG01X BG03X BG10X BK00Y CE00Y GC00 HA07 ──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 7 Identification symbol FI Theme coat ゛ (Reference) C08L 33/20 C08L 33/20 93/00 93/00 93/04 93/04 // B29K 9:00 33 : 00 86:00 B29L 31:48 F term (reference) 3B033 AB10 AC03 BA01 4F205 AA20E AA21E AA46 AA49 AC05 AH70 GA08 GB01 GC01 GF01 GW06 4J002 AC07W AF02Y BA00Y BG01X BG03X BG10X BK00Y CE00Y GC00 HA07
Claims (1)
ルとアクリル酸またはメタクリル酸との共重合体と、ロ
ジン酸樹脂またはテルペン系樹脂の少なくとも一方とを
配合したNBRラテックスを材料に用いて成形されてな
ることを特徴とするNBR製手袋。1. An NBR latex blended with a copolymer of an alkyl acrylate, acrylonitrile, acrylic acid or methacrylic acid, and at least one of a rosin acid resin and a terpene resin, and molded using a material as a material. Gloves made of NBR.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP9825799A JP3382879B2 (en) | 1999-04-06 | 1999-04-06 | NBR gloves |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP9825799A JP3382879B2 (en) | 1999-04-06 | 1999-04-06 | NBR gloves |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2000290816A true JP2000290816A (en) | 2000-10-17 |
| JP3382879B2 JP3382879B2 (en) | 2003-03-04 |
Family
ID=14214913
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP9825799A Expired - Fee Related JP3382879B2 (en) | 1999-04-06 | 1999-04-06 | NBR gloves |
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| Country | Link |
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Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2005000550A3 (en) * | 2003-06-27 | 2005-03-24 | Zeon Corp | Polymer alloy, crosslinked object, and fuel hose |
| JP5071389B2 (en) * | 2006-09-04 | 2012-11-14 | ショーワグローブ株式会社 | gloves |
-
1999
- 1999-04-06 JP JP9825799A patent/JP3382879B2/en not_active Expired - Fee Related
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2005000550A3 (en) * | 2003-06-27 | 2005-03-24 | Zeon Corp | Polymer alloy, crosslinked object, and fuel hose |
| JP5071389B2 (en) * | 2006-09-04 | 2012-11-14 | ショーワグローブ株式会社 | gloves |
Also Published As
| Publication number | Publication date |
|---|---|
| JP3382879B2 (en) | 2003-03-04 |
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