JPS6248741A - Electrically-conductive rubber composition of light color - Google Patents

Electrically-conductive rubber composition of light color

Info

Publication number
JPS6248741A
JPS6248741A JP18737885A JP18737885A JPS6248741A JP S6248741 A JPS6248741 A JP S6248741A JP 18737885 A JP18737885 A JP 18737885A JP 18737885 A JP18737885 A JP 18737885A JP S6248741 A JPS6248741 A JP S6248741A
Authority
JP
Japan
Prior art keywords
rubber
rubber composition
conductive rubber
electrically
glycol
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP18737885A
Other languages
Japanese (ja)
Inventor
Shohei Watanabe
渡邉 昌平
Mitsuyuki Miyake
三宅 光之
Yoshio Kanemitsu
金光 義雄
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nisshin Rubber Co Ltd
Original Assignee
Nisshin Rubber Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Nisshin Rubber Co Ltd filed Critical Nisshin Rubber Co Ltd
Priority to JP18737885A priority Critical patent/JPS6248741A/en
Publication of JPS6248741A publication Critical patent/JPS6248741A/en
Pending legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)
  • Conductive Materials (AREA)

Abstract

PURPOSE:An electrically-conductive rubber composition of light color causing a little drop in electrical conductivity in preservation and in use such as washing, etc., having no occurrence of rust, capable of producing all colors, obtained by blending rubber with a dihydric alcohol. CONSTITUTION:100pts.wt. natural rubber or any of various kinds of synthetic rubber is blended with 5-40pts.wt. dihydric alcohol having 50-6,000 average molecular weight, such as methylene glycol, ethylene glycol, diethylene glycol, polyethylene glycol or its mixture to give the aimed electrically-conductive rubber composition.

Description

【発明の詳細な説明】 C産業上の利用分野] 本発明はゴムに薬剤を添加して導電性を付与した明るい
色のゴム組成物に関するものである。
DETAILED DESCRIPTION OF THE INVENTION C. Industrial Application Field The present invention relates to a brightly colored rubber composition in which a chemical is added to rubber to impart conductivity.

[従来の技術] ゴムは、電気絶縁体であることが一般であり、そのため
に生ずる静電気帯電によって塵埃が付着したり、帯電し
た静電気が放電するときのスパークにより火災が発生し
たり、コンピューター誤動作事故を起したりするなど種
々の問題があるため、ゴムに導電性を付与することが行
なわれてきた。又、ゴムの弾性、強5度その他種々の特
性を生かしながら導電性を付与して機能を追加すること
により新しい分野へ発展してきた。
[Prior Art] Rubber is generally an electrical insulator, which causes dust to adhere to it due to static electricity, fires caused by sparks when charged static electricity discharges, and computer malfunction accidents. Since there are various problems such as the occurrence of electrical conductivity, attempts have been made to impart conductivity to rubber. In addition, it has developed into new fields by adding functions by adding conductivity while taking advantage of rubber's elasticity, strength, and other various properties.

従来、ゴムの導電性付与組成物としてカーボンブラック
が最も一般的であるが、これは黒色−色であり、明色は
得られない。カーボンブラック以外では、金属酸化物及
びその塩化物を使用するもの(特開昭Go−832H)
があり、明色は得られるが、塩化物がゴム表面に出た時
に鉄などの金属を錆さすので問題がある。
Conventionally, carbon black has been the most common composition for imparting electrical conductivity to rubber, but it is black in color and cannot provide a bright color. Other than carbon black, those using metal oxides and their chlorides (JP-A-Sho Go-832H)
Although a bright color can be obtained, there is a problem because when chloride comes out on the rubber surface, it rusts metals such as iron.

〔発明が解決しようとする問題点] 上記のように従来、ゴムに導電性を付与しようとすると
、黒色以外の明色では錆の問題があり。
[Problems to be Solved by the Invention] As mentioned above, conventionally, when trying to impart conductivity to rubber, there is a problem of rust in light colors other than black.

黒色のカーボンブラックを使用せざるを得なかった。本
発明はこのような問題点を解決し、導電性を減すること
なく、ファツション性が高く、また錆の発生がなく、保
管中及び洗濯等の使用中に導電性低下が′少なく、しか
も黒色はもとよりそれ以外のあらゆる色彩の色を出すこ
とができる明色導電性ゴム組成物を提供することを目的
とするものである。この明色導電性ゴム組成物は静電気
帯電防1ヒ用作業ぐつにも有用である。
I had no choice but to use black carbon black. The present invention solves these problems, has high fashionability without reducing conductivity, does not rust, has little decrease in conductivity during storage, washing, etc., and is black in color. It is an object of the present invention to provide a light-colored conductive rubber composition that can produce all other colors. This light colored conductive rubber composition is also useful in anti-static work shoes.

[問題点を解決するための手段] 上記問題点を解決し、発明の目的を達成するための本発
明の特徴とするところは、ゴム 100重量部に、二価
アルコールを5〜40重量部添加してなることを特徴と
する。ここで、ゴムとしては、天然ゴムや各種の合成ゴ
ムを使用することができ。
[Means for Solving the Problems] The present invention is characterized by the addition of 5 to 40 parts by weight of dihydric alcohol to 100 parts by weight of rubber. It is characterized by: Here, as the rubber, natural rubber and various synthetic rubbers can be used.

二価アルコールとしてはメチレングリコール、エチレン
グリコール、ジエチレングリコール、ポリエチレングリ
コール(例えば、平均分子量が400、1000.40
00.8000. 10000あるいは20000のポ
リエチレングリコール)、あるいはこれらの混合物を挙
げることができる。ゴムに二価アルコールを添加する方
法は、a−ル機を用いる等、常法により添加混合する。
Examples of dihydric alcohols include methylene glycol, ethylene glycol, diethylene glycol, and polyethylene glycol (e.g., average molecular weight of 400, 1000.40
00.8000. 10,000 or 20,000 polyethylene glycol) or a mixture thereof. The dihydric alcohol is added to the rubber by a conventional method such as using an A-R machine.

[実施例] 以下本発明に係る実施例により詳細に説明する。[Example] Hereinafter, the present invention will be explained in detail using examples.

アクリルニトリルブタジェンラバー ン株式会社製、二ボール1042 (商標))(以下N
BRという)にジエチレングリコール、ポリエチレング
リコール4000 (平均分子量4000)  (ライ
オン株式会社製)を添加したものについて説明する.第
1表は比較例Aと実施例1乃至3の配合割合を示した表
である。
Acrylic Nitrile Butadiene La Verne Co., Ltd., Ni-Ball 1042 (trademark)) (hereinafter N
The following describes a product in which diethylene glycol and polyethylene glycol 4000 (average molecular weight 4000) (manufactured by Lion Corporation) are added to BR (referred to as BR). Table 1 is a table showing the blending ratios of Comparative Example A and Examples 1 to 3.

第1表に示された配合薬品をロール機を用いて混合し、
24時間熟成を行ない、再びロール機で約21111厚
さのシートとし、 150度Cで20分間プレス加硫す
る.加硫後24時間以上経過した試料につい−て、体積
固有抵抗、表面抵抗を測定した結果は第1表の下2行の
通りである.測定機はジョンクルーク社製887ABで
、電圧発生機は横河電機製2853と同2861を使用
し、電圧500vで湿度50%の条件で測定した。
Mix the compounded chemicals shown in Table 1 using a roll machine,
After aging for 24 hours, the sheet is made into a sheet with a thickness of about 21111 mm again using a roll machine, and press-vulcanized at 150 degrees Celsius for 20 minutes. The bottom two rows of Table 1 show the results of measuring the volume resistivity and surface resistance of samples 24 hours or more after vulcanization. The measuring device was 887AB manufactured by John Kruk, and the voltage generators 2853 and 2861 manufactured by Yokogawa Electric were used, and the measurement was performed at a voltage of 500 V and humidity of 50%.

実施例1、2,3の試料を22時間常温の流水中に浸漬
した後、50度Cで30分乾燥し、常温で50%湿度の
デシケータ−で2時間冷却し、体積固有抵抗、表面抵抗
を測定し、それを5回繰り返して流水試験を行なった.
結果を第1図、第2図に示す。
The samples of Examples 1, 2, and 3 were immersed in running water at room temperature for 22 hours, dried at 50 degrees C for 30 minutes, cooled for 2 hours in a desiccator at room temperature and 50% humidity, and measured for volume resistivity and surface resistance. was measured and repeated five times to perform a running water test.
The results are shown in Figures 1 and 2.

この試験結果よりジエチレングリコールを添加したもの
の常態での導電性は、ポリエチレングリコールを添加し
たものよりも良いが、流水中の浸漬時間が長くなると導
電性が低下する傾向が見らられる.これは水によりジエ
チレングリコールが溶解され流出した結果と考えられる
.逆にポリエチレングリコールは,常態時の導電性はジ
エチレングリコールより悪いが,流木時間が長くなって
も導電性の低下はほとんどみられない。これらのことか
らジエチレングリコールとポリエチレングリコールを併
用し、分子量分布をもたせることで常態時及び水による
低下率を改善することができる。
The test results show that the conductivity under normal conditions of the diethylene glycol-added product is better than that of the polyethylene glycol-added product, but there is a tendency for the conductivity to decrease as the immersion time in running water increases. This is thought to be the result of diethylene glycol being dissolved by water and flowing out. On the other hand, polyethylene glycol has worse conductivity than diethylene glycol under normal conditions, but there is almost no decrease in conductivity even when driftwood is left for a long time. For these reasons, by using diethylene glycol and polyethylene glycol in combination to provide a molecular weight distribution, it is possible to improve the rate of decrease under normal conditions and due to water.

なお、ゴム 100重量部に対して、二価アルコールが
5重量部以下では殆んど効果がなく、50重量部以上に
なると表面に浮きでたり、ゴムとしての特性低下が大き
くなるので好ましくなく,5〜40重量部が適している
It should be noted that if the dihydric alcohol is less than 5 parts by weight per 100 parts by weight of rubber, it will have almost no effect, and if it is more than 50 parts by weight, it will float on the surface and the properties as a rubber will greatly deteriorate, which is not preferable. 5 to 40 parts by weight are suitable.

第2表は、本発明に係る他の実施例(実施例4)と先に
挙げた特開昭80−63236による組成物(比較例B
)との比較を示したものである。
Table 2 shows another example (Example 4) according to the present invention and the composition according to JP-A-80-63236 mentioned above (Comparative Example B).
).

実施例4の試料は次のようにして作った。6吋ロールを
用い、50〜60度Cの温度で、ロールを締め切り、N
BRのみを5分間素線りをした後、ロール間隔を3重讃
とし、NBRを巻付け、シリカの全量の2分の1と、亜
鉛華、ジオクチルフタ−レート、ポリエチレングリコー
ル、芒硝を混入する。次にジエチレングリコールと水を
予め混合しておいたジエチレングリコール水とシリカの
残り2分の1とを混合しながらロール上へ投入していく
、これが半分程度練り込まれた時に、テトラメチルチウ
ラムモノサルファイドとジベンゾチアゾールを投入し、
また他のすべての薬品を混入してロールより外し、ロー
ルを再び締め切り、3回薄通しを行なった後、ロール間
隔を5層−とし、切り出す、これを24時間熟成し、再
びロール機を用い約2mm厚さのシートとし、 150
度Cで20分間プレス加硫し、加硫後24時間以上経過
した試料につ第2表 いて、体積固有抵抗、表面抵抗を測定した。結果は第2
表下2行の通りである。
The sample of Example 4 was made as follows. Using a 6-inch roll, close the roll at a temperature of 50 to 60 degrees C and apply N
After stranding only BR for 5 minutes, set the roll interval to 3 times, wrap NBR, and mix one-half of the total amount of silica, zinc white, dioctyl phthalate, polyethylene glycol, and Glauber's salt. . Next, diethylene glycol water, which has been pre-mixed with diethylene glycol and water, is mixed with the remaining half of the silica and poured onto the roll. When about half of this has been kneaded, tetramethylthiuram monosulfide and Add dibenzothiazole,
Also, all other chemicals are mixed in and removed from the roll, the roll is closed again, and the roll is passed through three times.The roll interval is set to 5 layers, and the cut is cut out.This is aged for 24 hours, and then the roll machine is used again. A sheet approximately 2mm thick, 150
Press vulcanization was carried out at a temperature of 20° C. for 20 minutes, and the volume resistivity and surface resistance of the second sample were measured after 24 hours or more had elapsed after vulcanization. The result is second
As shown in the bottom two lines of the table.

次いで、試料を22時間常温の流水中に浸漬した後、5
0度Cで30分乾燥し、常温で50%湿度のデシケータ
−で2時間冷却し、体積固有抵抗を測定し、それを5回
繰り返して流水試験を行なった。
Next, after immersing the sample in running water at room temperature for 22 hours,
The sample was dried at 0 degrees Celsius for 30 minutes, cooled for 2 hours in a desiccator at room temperature and 50% humidity, and the volume resistivity was measured, which was repeated 5 times to conduct a running water test.

結果を第3図に示す。The results are shown in Figure 3.

また、試料を50度Cのギアーオーブン中で22時間乾
燥を行ない、常温で50%湿度のデシケータ−で1時間
冷却し、体積固有抵抗を測定し、それを5回繰り返して
乾燥試験を行なった。結果を第4図に示す。
In addition, the sample was dried for 22 hours in a gear oven at 50 degrees Celsius, cooled for 1 hour in a desiccator at room temperature and 50% humidity, and the volume resistivity was measured, which was repeated 5 times to conduct a drying test. . The results are shown in Figure 4.

更にまた、鉄板をプラストして表面研磨を行ない、新し
い面として、そのヒに試料を置き1重しを載せ、室温で
放置して錆発生試験を行なった。
Furthermore, an iron plate was plastered and the surface was polished, and as a new surface, a sample was placed on the plate, one weight was placed on it, and the plate was left at room temperature to perform a rust generation test.

発生した錆の面積比率を第3表に示す。Table 3 shows the area ratio of generated rust.

以上の結果から、本発明に係る実施例4は、比較例Bと
比較して流水試験と乾燥試験の体積固有抵抗については
有意差は認められず、同等であるが、錆の発生状況は実
施例の方が良いことが分る。比較例Bは、保管中及び洗
濯等の使用中に導電性低下の少ない配合であるが、本発
明に係る組成物は更に優れていることが分る。
From the above results, Example 4 according to the present invention is equivalent to Comparative Example B with no significant difference in volume resistivity in running water test and dry test, but the rust occurrence situation was I find that an example is better. Although Comparative Example B has a formulation that causes less conductivity deterioration during storage and use such as washing, it can be seen that the composition according to the present invention is even better.

なお、本発明に係る組成物は、その配合において色素を
混入すれば導電性を低下させることなく、ゴムとしてあ
らゆる色彩の色を出すことができ、ファツション性を高
め、しかも、JIST−8103(静電気帯電防止用作
業ぐつ)の規格を充分満足させることができた。
The composition according to the present invention can produce all kinds of colors as a rubber without reducing conductivity if a pigment is mixed in the composition, improves fashionability, and meets JIST-8103 (static electricity). The product was able to fully satisfy the standards for antistatic work shoes.

し発明の効果] 本発明は上記のように構成されているので、本発明に係
る明色導電性ゴム組成物は、導電性を有し、この導電性
は保管中及び洗濯等の使用中に低下が少なく、錆の発生
がなく、しかも黒色はもとよりそれ以外のあらゆる色彩
の色を出すことができ、ファツション性が高い製品を製
造することができるという効果を有する。従って本発明
に係る明色導電性ゴム組成物は種々の用途に使用される
が、特に静電気帯電防止用作業ぐつの製造に有用である
[Effects of the Invention] Since the present invention is configured as described above, the light-colored conductive rubber composition according to the present invention has conductivity, and this conductivity is maintained during storage and during use such as washing. It has the effect that it has little deterioration, does not cause rust, can produce not only black but also all other colors, and can produce highly fashionable products. Therefore, the light-colored conductive rubber composition according to the present invention is used for various purposes, but is particularly useful for manufacturing work shoes for preventing static electricity.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図、第2図は、実施例1.2.3の流水試験結果を
示す図、83図は、実施例4と比較例Bの流水試験結果
、第4図は実施例4と比較例Bの乾燥試験結果を示す図
である。 代理人 弁理士 小 1)治 親 絶1図 第2図 常g      1    2J     45回第3
図 第4図
Figures 1 and 2 show the running water test results of Example 1.2.3, Figure 83 shows the running water test results of Example 4 and Comparative Example B, and Figure 4 shows the running water test results of Example 4 and Comparative Example. It is a figure showing the drying test result of B. Agent Patent Attorney Elementary School 1) Chi Zetsu 1 Figure 2 Figure 2 Jou g 1 2J 45th No. 3
Figure 4

Claims (2)

【特許請求の範囲】[Claims] (1)ゴム100重量部に、二価アルコールを5〜40
重量部添加してなることを特徴とする明色導電性ゴム組
成物。
(1) Add 5 to 40 parts of dihydric alcohol to 100 parts by weight of rubber.
1. A light-colored conductive rubber composition, characterized in that the composition is made by adding parts by weight.
(2)二価アルコールが平均分子量50〜6000の二
価アルコールであることを特徴とする特許請求の範囲第
1項記載の明色導電性ゴム組成物。
(2) The light-colored conductive rubber composition according to claim 1, wherein the dihydric alcohol is a dihydric alcohol having an average molecular weight of 50 to 6,000.
JP18737885A 1985-08-28 1985-08-28 Electrically-conductive rubber composition of light color Pending JPS6248741A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP18737885A JPS6248741A (en) 1985-08-28 1985-08-28 Electrically-conductive rubber composition of light color

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP18737885A JPS6248741A (en) 1985-08-28 1985-08-28 Electrically-conductive rubber composition of light color

Publications (1)

Publication Number Publication Date
JPS6248741A true JPS6248741A (en) 1987-03-03

Family

ID=16204964

Family Applications (1)

Application Number Title Priority Date Filing Date
JP18737885A Pending JPS6248741A (en) 1985-08-28 1985-08-28 Electrically-conductive rubber composition of light color

Country Status (1)

Country Link
JP (1) JPS6248741A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH02265055A (en) * 1989-04-06 1990-10-29 Nec Corp Controller for distance between magnetic head and disk
US5714533A (en) * 1994-10-11 1998-02-03 Bridgestone Corporation Rubber composition improved in charging property and pneumatic tire produced by making use of the same

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4832769A (en) * 1971-09-02 1973-05-02
JPS59206444A (en) * 1983-05-04 1984-11-22 Kokoku Gomme Kogyo Kk Electroconductive polymer composition
JPS59217782A (en) * 1983-05-26 1984-12-07 Lion Corp Antistatic agent for thermoplastic resin

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4832769A (en) * 1971-09-02 1973-05-02
JPS59206444A (en) * 1983-05-04 1984-11-22 Kokoku Gomme Kogyo Kk Electroconductive polymer composition
JPS59217782A (en) * 1983-05-26 1984-12-07 Lion Corp Antistatic agent for thermoplastic resin

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH02265055A (en) * 1989-04-06 1990-10-29 Nec Corp Controller for distance between magnetic head and disk
US5714533A (en) * 1994-10-11 1998-02-03 Bridgestone Corporation Rubber composition improved in charging property and pneumatic tire produced by making use of the same

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