JPH05320425A - Polychloroprene rubber composition - Google Patents

Polychloroprene rubber composition

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Publication number
JPH05320425A
JPH05320425A JP12634792A JP12634792A JPH05320425A JP H05320425 A JPH05320425 A JP H05320425A JP 12634792 A JP12634792 A JP 12634792A JP 12634792 A JP12634792 A JP 12634792A JP H05320425 A JPH05320425 A JP H05320425A
Authority
JP
Japan
Prior art keywords
rubber composition
polychloroprene rubber
weight
parts
carbon black
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
JP12634792A
Other languages
Japanese (ja)
Inventor
Keiji Takano
敬二 高野
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.)
Furukawa Electric Co Ltd
Original Assignee
Furukawa Electric 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 Furukawa Electric Co Ltd filed Critical Furukawa Electric Co Ltd
Priority to JP12634792A priority Critical patent/JPH05320425A/en
Publication of JPH05320425A publication Critical patent/JPH05320425A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To improve extrusion moldability and mechanical and electrical insulation properties by blending a polychloroprene rubber, a carbon black having a specific particle size, a fiber and a vulcanizing agent. CONSTITUTION:100 pts.wt. polychroloprene rubber is compounded with 10-50 pts.wt. carbon black having an average particle size of 85mum or less, 0.5-3 pts.wt. at least one fiber selected from among carbon, ceramic and aramid fibers and a small amount of vulcanizing agent, optionally together with a vulcanization accelerator, a softener and a filler, and kneaded.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明はキャプタイヤケーブル等
のシース材料として好適なポリクロロプレンゴム組成に
関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a polychloroprene rubber composition suitable as a sheath material for captyre cables and the like.

【0002】[0002]

【従来の技術】一般にポリクロロプレンゴムは耐油性、
耐薬品性に優れているため、例えばキャプタイヤケーブ
ル等のシース材料として広く使用されているものであ
る。このキャプタイヤケーブルは主として仮設現場用ケ
ーブルと使用されるためその使用中に種々の外傷をうけ
易い。このためケーブルのシース材料には高度の機械的
性能を必要としているものである。
2. Description of the Related Art Generally, polychloroprene rubber has oil resistance,
Since it has excellent chemical resistance, it is widely used as a sheath material for, for example, a captyre cable. Since this cabtire cable is mainly used as a cable for temporary construction sites, it is susceptible to various external damages during its use. Therefore, the sheath material of the cable requires a high degree of mechanical performance.

【0003】かかる機械的性能の要求に応えるために、
従来ポリクロロプレンゴムに各種補強剤を添加している
ものであるが、その中でも補強効果が最も大きいことか
らカーボンブラックが汎用されている。
In order to meet the demand for such mechanical performance,
Conventionally, various reinforcing agents have been added to polychloroprene rubber. Among them, carbon black is widely used because it has the largest reinforcing effect.

【0004】然しながら上記の如く機械的性能を向上せ
しめる目的にてポリクロロプレンゴムに多量のカーボン
ブラックを配合し混練した場合、未加硫ゴムのムーニー
粘度の上昇による耐スコーチ性の悪化等の問題を生ず
る。また近年キャプタイヤケーブルのシース材料として
漏電事故を防止するために電気絶縁性の良好であること
も要求されている。然しポリクロロプレンゴムにカーボ
ンブラックを多量に配合したポリクロロプレンゴム組成
物によるシース材料は電気絶縁性が低下するため、この
点からも好ましくない。
However, when a large amount of carbon black is mixed and kneaded with polychloroprene rubber for the purpose of improving the mechanical performance as described above, problems such as deterioration of scorch resistance due to increase in Mooney viscosity of unvulcanized rubber occur. Occurs. Further, in recent years, it has also been required that the sheath material of a captyre cable has good electric insulation in order to prevent an electric leakage accident. However, the sheath material made of the polychloroprene rubber composition in which a large amount of carbon black is blended with the polychloroprene rubber has a low electric insulating property, and is also not preferable in this respect.

【0005】このようにポリクロロプレンゴムにカーボ
ンブラックを配合して、その機械的強度を改良せしめん
とする場合その配合量が少量の場合には得られる組成物
に十分な機械的強度を付与せしめることが出来ず、更に
得られる組成物は押出成形時に変形或は垂れ下りの現象
を呈するなど押出成形物の形状維持性が低下する。又多
量に配合した場合には耐スコーチ性及び電気絶縁性が劣
るというカーボンブラックの配合量に基く二律背反的課
題を生じ、この相反する課題を解決したポリクロロプレ
ンゴム組成物は未だ見出されていないのである。
When the carbon black is blended with the polychloroprene rubber to improve its mechanical strength as described above, a sufficient amount of mechanical strength is imparted to the resulting composition when the amount of the blend is small. In addition, the obtained composition exhibits a phenomenon of deformation or sagging during extrusion molding, resulting in deterioration of shape retention of the extrusion molded article. In addition, when compounded in a large amount, scorch resistance and electrical insulation are inferior, which causes a contradictory problem based on the compounding amount of carbon black, and a polychloroprene rubber composition that solves these contradictory problems has not yet been found. Of.

【0006】[0006]

【発明が解決しようとする課題】本発明はかかる現状に
鑑み鋭意研究を行った結果、押出成形性が良好にして、
その成形物が優れた機械的性能及び電気絶縁性を有する
ポリクロロプレンゴム組成物を開発したものである。
DISCLOSURE OF THE INVENTION In the present invention, as a result of intensive studies in view of the present situation, as a result of improving extrusion moldability,
The molded product has developed a polychloroprene rubber composition having excellent mechanical performance and electrical insulation.

【0007】[0007]

【課題を解決するための手段】本発明のポリクロロプレ
ンゴム組成物はポリクロロプレンゴム100重量部に対
して平均粒径85mμ以下のカーボンブラック10〜5
0重量部、炭素繊維、セラミック繊維、アラミド繊維の
群から選ばれた繊維の内何れか1種又は2種以上の混合
物0.5〜3重量部及び少量の加硫剤を夫々配合して練
和したことを特徴とするものである。
The polychloroprene rubber composition of the present invention comprises carbon blacks 10 to 5 having an average particle diameter of 85 mμ or less with respect to 100 parts by weight of polychloroprene rubber.
0 parts by weight, 0.5 to 3 parts by weight of a mixture of any one or two or more kinds of fibers selected from the group of carbon fibers, ceramic fibers and aramid fibers and a small amount of a vulcanizing agent are mixed and kneaded. It is characterized by being harmonized.

【0008】[0008]

【作用】本発明においてポリクロロプレンゴムとしては
一般に市販されているものを用いればよく、例えばネオ
プレンTW(昭和電工(株)社及びデュポン社製、商品
名)、スカイプレンE−33(トーソ(株)社製、商品
名)をあげることができる。
In the present invention, as the polychloroprene rubber, those commercially available may be used, for example, Neoprene TW (trade name, manufactured by Showa Denko KK and DuPont), SKYPRENE E-33 (Toso (stock) ) Company name, trade name).

【0009】又本発明は補強用としてカーボンブラック
を添加するものであるが、その形状において特に平均粒
径を85mμ以下のものに限定しているものである。そ
の理由は平均粒径が85mμを超えたものを使用した場
合にはポリクロロプレンゴム組成物の機械的性能が十分
に向上しないためである。
In the present invention, carbon black is added for reinforcement, but the shape is limited to those having an average particle diameter of 85 mμ or less. The reason is that the mechanical performance of the polychloroprene rubber composition is not sufficiently improved when an average particle size of more than 85 mμ is used.

【0010】このカーボンブラックとしては例えばダイ
アブラックSH(三菱化成(株)社製、商品名 平均粒
径22〜30mμ)、旭#55(旭カーボン(株)製、
商品名 平均粒径49〜84mμ)をあげることが出来
る。
Examples of the carbon black include Diablack SH (manufactured by Mitsubishi Kasei Co., Ltd., trade name average particle size 22 to 30 mμ), Asahi # 55 (manufactured by Asahi Carbon Co., Ltd.,
The average particle size of the product is 49 to 84 mμ).

【0011】而して発明ではこのカーボンブラックの配
合量をポリクロロプレンゴム100重量部に対し10〜
50重量部に限定したものであるが、その理由は10重
量部未満の場合には得られるポリクロロプレンゴム組成
物の機械的性能が向上せず又50重量部を超えて多量に
配合した場合には上記組成物の電気絶縁性が低下するた
めである。
In the invention, therefore, the amount of the carbon black compounded is 10 to 100 parts by weight of polychloroprene rubber.
It is limited to 50 parts by weight, but the reason is that when it is less than 10 parts by weight, the mechanical performance of the obtained polychloroprene rubber composition is not improved, and when it is blended in a large amount exceeding 50 parts by weight. Is because the electrical insulation of the above composition is reduced.

【0012】又本発明では特に炭素繊維、セラミック繊
維、アラミド繊維の群から選ばれた1種の繊維又は2種
以上の混合繊維を添加しているものであるが、これらの
繊維を配合することによりポリクロロプレンゴム組成物
の機械的性能を著しく向上せしめることが出来るためで
ある。
In the present invention, in particular, one kind of fiber selected from the group of carbon fiber, ceramic fiber and aramid fiber or a mixed fiber of two or more kinds is added, but these fibers should be blended. This is because the mechanical performance of the polychloroprene rubber composition can be remarkably improved.

【0013】然しこれらの繊維の配合量についても、ポ
リクロロプレンゴム100重量部に対し0.5〜30重
量部と限定するものであり、0.5重量部未満の場合に
は、得られるポリクロロプレンゴム組成物の機械的強度
の向上が薄く、30重量部を超えて多量に配合した場合
には得られる組成物の機械的伸びが低下するためであ
る。
However, the blending amount of these fibers is also limited to 0.5 to 30 parts by weight with respect to 100 parts by weight of polychloroprene rubber, and when it is less than 0.5 parts by weight, the polychloroprene obtained is obtained. This is because the improvement in mechanical strength of the rubber composition is thin, and the mechanical elongation of the composition obtained is reduced when the rubber composition is compounded in a large amount in excess of 30 parts by weight.

【0014】更に本発明では少量の加硫剤を添加して加
硫するものであるが、この加硫剤としては例えば酸化亜
鉛、酸化マグネシウム、酸化鉛をあげることが出来る
が、特に酸化亜鉛と酸化マグネシウムとを併用すること
が好ましい。
Further, in the present invention, a small amount of a vulcanizing agent is added for vulcanization. Examples of the vulcanizing agent include zinc oxide, magnesium oxide and lead oxide. It is preferable to use magnesium oxide together.

【0015】その他本発明のポリクロロプレンゴム組成
物には、上記の成分以外にも必要に応じて加硫促進剤例
えばエチレンチオウレア(川口化学(株)社製、商品名
アクセル22)、テトラメチルチウラムジスルフイド
(大内新興(株)社製、商品名 ノクセラーTT)、ジ
ブチルジチオカルバミン酸ニッケル(大内新興(株)社
製、ノクラックNBC)、軟化剤例えばアルキルナフタ
レン樹脂(ケンリッチケミカル社製、商品名 ケンフレ
ックスA)、充填剤例えばハードクレー(米国バンダー
ビルト社製、商品名 デキンクレー)、タルク、炭酸カ
ルシウム等を配合してもよい。
Others In addition to the above components, the polychloroprene rubber composition of the present invention may optionally contain a vulcanization accelerator such as ethylenethiourea (Kawaguchi Chemical Co., Ltd., trade name Axel 22), tetramethylthiuram. Disulfide (manufactured by Ouchi Shinko Co., Ltd., trade name Nox Cler TT), nickel dibutyldithiocarbamate (manufactured by Ouchi Shinko Co., Ltd., Nocrac NBC), softeners such as alkylnaphthalene resin (Kenrich Chemical Co., Ltd., You may mix | blend brand name Kenflex A), a filler, for example, hard clay (made by Vanderbilt Co., USA, brand name Dekin clay), talc, calcium carbonate, and the like.

【0016】[0016]

【実施例】[実施例(1)〜(5)及び比較例(1)〜
(7)]表1に示す組成に基いて、各成分をバンバリー
ミキサーにより十分に混練りを行って本発明のポリクロ
ロプレンゴム組成物及び比較例ポリクロロプレンゴム組
成物をえた。
EXAMPLES [Examples (1) to (5) and Comparative Examples (1) to
(7)] Based on the composition shown in Table 1, the respective components were sufficiently kneaded with a Banbury mixer to obtain a polychloroprene rubber composition of the present invention and a polychloroprene rubber composition of a comparative example.

【0017】斯くしてえた本発明のポリクロロプレンゴ
ム組成物及び比較例ポリクロロプレンゴム組成物につい
てその性能、即ち耐スコーチ性、未加硫物の変形率、引
張強さ、伸び体積抵抗率及び電線磨耗性を夫々測定し
た。その結果は表1に併記した通りである。
The properties of the polychloroprene rubber composition of the present invention and the polychloroprene rubber composition of Comparative Example thus obtained are as follows: scorch resistance, unvulcanized product deformation rate, tensile strength, elongation volume resistivity and electric wire. Abrasivity was measured respectively. The results are as shown in Table 1.

【0018】[0018]

【表1】 なお表1中における組成の数値は何れも重量部を示す。[Table 1] The numerical values of the compositions in Table 1 are all parts by weight.

【0019】又表中における組成の各成分品は下記
(A)に示す会社による製品であり、又ポリクロロプレ
ンゴム組成物の性能は下記(B)に示す方法に基き測定
した。
Each component having the composition shown in the table is a product by a company shown in (A) below, and the performance of the polychloroprene rubber composition was measured based on the method shown in (B) below.

【0020】記(A) (1)炭素繊維:ブラノック(日本石油(株)社製、商
品名) (2)セラミック繊維:イビラール(イビデン社製、商
品名) (3)アラミド繊維:(デュポン社製、商品名) (4)旭サーマル:旭カーボンブラック社製、カーボン
ブラック平均粒径90〜206mμ (5)酸化亜鉛:1号亜鉛華(三井金属(株)製、商品
名) (6)酸化マグネシウム:キョウマグ150(協和化学
(株)製、商品名) 記(B) (1)スコーチ性: JIS K6300に準じ、ムーニー、スコーチ試験を
行った。即ち125℃スモールローター(MS125
℃)で未加硫ゴム組成物のムーニースコッチタイムの5
ポイントアップ時間(t5 )を測定し、耐スコーチ性を
判定した。この5ポイントアップ(t5 )があまり短い
と保存時及び押出時にスコーチを発生することになる。
Note (A) (1) Carbon fiber: Branock (manufactured by Nippon Oil Co., Ltd., trade name) (2) Ceramic fiber: Ibiral (manufactured by Ibiden, trade name) (3) Aramid fiber: (Dupont (4) Asahi Thermal: Asahi Carbon Black Co., Ltd., carbon black average particle size 90 to 206 mμ (5) Zinc oxide: No. 1 zinc white (Mitsui Kinzoku Co., Ltd., trade name) (6) Oxidation Magnesium: Kyomag 150 (Kyowa Chemical Co., Ltd., trade name) Note (B) (1) Scorch property: According to JIS K6300, Mooney and scorch tests were conducted. That is, 125 ° C small rotor (MS125
5) of the unvulcanized rubber composition Mooney Scotch time
The point-up time (t 5 ) was measured to determine the scorch resistance. If this 5-point increase (t 5 ) is too short, scorch will occur during storage and extrusion.

【0021】(2)未加硫ゴム組成物の変形率 未加硫ゴム組成物の変形率を測定し、変形率の大小によ
り押出成形体の形状保存性を判定した。未加硫ゴム組成
物の変形率は次の方法により測定した。即ち混練直後の
練生地から縦10mm×横10mm×厚さ10mmの試
験片を切り取り、こり試験片に100g/cm2 の荷重
を100℃にて10分間負荷し、負荷後の厚さを測定し
た。この測定値に基き下記式により変形率を算出した。
(2) Deformation rate of unvulcanized rubber composition The deformation rate of the unvulcanized rubber composition was measured, and the shape-preserving property of the extruded product was judged by the magnitude of the deformation rate. The deformation rate of the unvulcanized rubber composition was measured by the following method. That is, a test piece having a length of 10 mm, a width of 10 mm, and a thickness of 10 mm was cut out from the kneading material immediately after kneading, and a load of 100 g / cm 2 was applied to the dust test piece at 100 ° C. for 10 minutes, and the thickness after the load was measured .. Based on this measured value, the deformation rate was calculated by the following formula.

【0022】 変形率=初期厚さ−負荷後の厚さ/初期厚さ×100 この変形率が30%を超えると押出時に変形又は垂れ下
りを生ずることになる。
Deformation rate = initial thickness-thickness after loading / initial thickness × 100 If this deformation rate exceeds 30%, deformation or sagging occurs during extrusion.

【0023】(3)引張り強さ及び伸び 未加硫ゴム組成物を150℃にて20分間加硫し成形温
度150℃、成形圧力150kg/mm2 の条件にて厚
さ2mmのシートを得た。このシートからJIS K6
301に準じて3号ベンダル片を切り取り、引張り強さ
と伸びを測定した。
(3) Tensile Strength and Elongation The unvulcanized rubber composition was vulcanized at 150 ° C. for 20 minutes to obtain a sheet having a thickness of 2 mm under the conditions of a molding temperature of 150 ° C. and a molding pressure of 150 kg / mm 2 . .. From this sheet JIS K6
A No. 3 bendal piece was cut out in accordance with 301, and the tensile strength and the elongation were measured.

【0024】(4)電気絶縁性 JIS K6911に準じてえた試験片について、体積
抵抗率を測定した。
(4) Electric insulation The volume resistivity of the test piece obtained according to JIS K6911 was measured.

【0025】(5)電線磨耗性 断面積5.5mm2 の電気導体の周囲に未加硫ゴム組成
物を厚さ3mmになるように押出被覆し、これを150
℃にて20分間加硫した後、30cmの長さに切断し試
験片を得た。ついでこの試験片JIS K3005磁石
磨耗試験機により400rpmの条件で擦った後の磨耗
量(cc)を測定した。
(5) Abrasion resistance of electric wire An unvulcanized rubber composition was extrusion-coated to a thickness of 3 mm around an electric conductor having a cross-sectional area of 5.5 mm 2.
After vulcanization at 20 ° C. for 20 minutes, it was cut into a length of 30 cm to obtain a test piece. Then, the abrasion amount (cc) of the test piece after rubbing under the condition of 400 rpm was measured by a JIS K3005 magnet abrasion tester.

【0026】表1より明らかな如く、実施例(1)〜
(5)に示す本発明のポリクロロプレンゴム組成物は耐
久スコーチ性が良好にして且つ未加硫ゴム組成物の変形
率が小さく、しかも機械的性能の強度及び伸びが大きい
と共に電気絶縁性及び磨耗性に優れていることを示し
た。これに対し比較例のポリクロロプレンゴム組成物は
本発明のポリクロロプレンゴム組成物の何れの性能より
劣ることが認められた。
As is clear from Table 1, Examples (1) to
The polychloroprene rubber composition of the present invention shown in (5) has a good durability scorch property, a small deformation ratio of the unvulcanized rubber composition, a large mechanical strength and elongation, and an electrical insulating property and wear resistance. It was shown to have excellent properties. In contrast, the polychloroprene rubber composition of Comparative Example was found to be inferior to any performance of the polychloroprene rubber composition of the present invention.

【0027】[0027]

【発明の効果】本発明のポリクロロプレンゴム組成物
は、押出成形性を損うことなく、優れた機械的性能及び
電気的性能を有するため、キャプタイヤケーブル等のシ
ース材料として好適なものであり、ケーブル使用時にお
けるシースの損傷度合を大幅に小さくすることが出来う
ると共に電気絶縁性に優れているため漏電事故も皆無に
なる等工業上有用なものである。
The polychloroprene rubber composition of the present invention has excellent mechanical performance and electrical performance without impairing extrusion moldability, and is therefore suitable as a sheath material for cabtire cables and the like. The degree of damage to the sheath when the cable is used can be greatly reduced, and since it has excellent electrical insulation properties, it is industrially useful, such that there is no electrical leakage accident.

───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.5 識別記号 庁内整理番号 FI 技術表示箇所 C08L 77:10) ─────────────────────────────────────────────────── ─── Continuation of front page (51) Int.Cl. 5 Identification code Office reference number FI technical display area C08L 77:10)

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 ポリクロロプレンゴム100重量部に対
して平均粒径85mμ以下のカーボンブラック10〜5
0重量部、炭素繊維、セラミック繊維、アラミド繊維の
群から選ばれた繊維の内、何れか1種又は2種以上の混
合物を0.5〜3重量部及び少量の加硫剤を夫々配合し
て練和したことを特徴とするポリクロロプレンゴム組成
物。
1. Carbon blacks 10 to 5 having an average particle diameter of 85 mμ or less based on 100 parts by weight of polychloroprene rubber.
0 to 3 parts by weight of a fiber selected from the group consisting of carbon fibers, ceramic fibers, and aramid fibers, and 0.5 to 3 parts by weight of a mixture of two or more kinds, and a small amount of a vulcanizing agent, respectively. A polychloroprene rubber composition characterized by being kneaded together.
JP12634792A 1992-05-19 1992-05-19 Polychloroprene rubber composition Pending JPH05320425A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP12634792A JPH05320425A (en) 1992-05-19 1992-05-19 Polychloroprene rubber composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP12634792A JPH05320425A (en) 1992-05-19 1992-05-19 Polychloroprene rubber composition

Publications (1)

Publication Number Publication Date
JPH05320425A true JPH05320425A (en) 1993-12-03

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Family Applications (1)

Application Number Title Priority Date Filing Date
JP12634792A Pending JPH05320425A (en) 1992-05-19 1992-05-19 Polychloroprene rubber composition

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JP (1) JPH05320425A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103374157A (en) * 2013-06-21 2013-10-30 安徽荣玖光纤通信科技有限公司 Flame-retardant cable sheath material and preparation method thereof

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103374157A (en) * 2013-06-21 2013-10-30 安徽荣玖光纤通信科技有限公司 Flame-retardant cable sheath material and preparation method thereof

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