JPH0350779B2 - - Google Patents

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Publication number
JPH0350779B2
JPH0350779B2 JP58004655A JP465583A JPH0350779B2 JP H0350779 B2 JPH0350779 B2 JP H0350779B2 JP 58004655 A JP58004655 A JP 58004655A JP 465583 A JP465583 A JP 465583A JP H0350779 B2 JPH0350779 B2 JP H0350779B2
Authority
JP
Japan
Prior art keywords
rubber
parts
core
composition
weight
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.)
Expired - Lifetime
Application number
JP58004655A
Other languages
Japanese (ja)
Other versions
JPS59129238A (en
Inventor
Kunyasu Horiuchi
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.)
Sumitomo Rubber Industries Ltd
Original Assignee
Sumitomo Rubber Industries 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 Sumitomo Rubber Industries Ltd filed Critical Sumitomo Rubber Industries Ltd
Priority to JP465583A priority Critical patent/JPS59129238A/en
Publication of JPS59129238A publication Critical patent/JPS59129238A/en
Publication of JPH0350779B2 publication Critical patent/JPH0350779B2/ja
Granted legal-status Critical Current

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Description

【発明の詳細な説明】[Detailed description of the invention]

本発明はテニスボールのコアー用ゴム組成物に
関する。 一般にゴム組成物には、配合剤の混ざり易さや
分散性の向上、ゴム流れを良くして抽出、圧延な
どの成形作業を容易にするために、軟化剤が必要
とされ、ステアリン酸、パルミチン酸などの高級
脂肪酸、棉実油、ヒマシ油などの高級脂肪酸エス
テル、パインタール、トール油などの植物油系軟
化剤、スピンドル油、プロセスオイルなどの石油
系軟化剤などが配合されているが、テニスボール
のコアー用ゴム組成物においては、上記のような
軟化剤はコアー特性で重要なコンプレツシヨンを
大きくする(つまり、コアーを軟らかくする)と
いう欠点がある。 そこで、加硫剤を増量して加硫程度を高くし適
正なコンプレツシヨンになるようにしているの
が、加硫剤の増量はコンプレツシヨンを小さく
し、コアーを硬くさせて、テニスボールにおいて
は耐久性やフイーリング(打球感)を低下させる
ことになる。 本発明はそのような事情に鑑み、従来の軟化剤
に代えて低分子量の液状ポリイソプレンゴムを用
いることにより、未加硫時のゴムの加工性を改善
し(つまり、配合剤の混ざり易さや分散性を向上
させ、ゴムの流れを良くして抽出、圧延などの成
形作業性を向上させる)、かつ加硫剤の増量を伴
なうことなく適正なコンプレツシヨンが得られる
ようにしたものである。 すなわち、本発明は天然ゴム100部(重量部、
以下同様)に対して平均分子量20000〜70000の液
状ポリイソプレンゴム1〜7部、酸化亜鉛3〜20
部、充填剤20〜60部、硫黄2〜5部および促進剤
1〜5部を配合したことを特徴とするテニスボー
ルのコアー用ゴム組成物である。 本発明において液状ポリイソプレンゴムは未加
硫時におけるゴムの加工性を改善する作用を期待
して使用するものであるが、この液状ポリイソプ
レンゴムは、架橋にまつたく関与しない従来の軟
化剤とは異なり、加硫剤によつて加硫され、加硫
後はそれ自身も多少のゴム状弾性を有するように
なるので、従来の軟化剤のようにゴム特性の大き
な低下を引きおこすことがなく、また未加硫時の
ゴムの加工性改善効果も良好で、軟化剤として充
分に使用できるものである。 本発明において液状ポリイソプレンゴムは、平
均分子量が20000〜70000の範囲のものを用いる。
これは平均分子量が20000未満のものは加硫ゴム
の物性を低下させ、逆に70000を超えるものは混
ざり易さ、分散性、抽出などの成形作業性を向上
させる効果が少ないからである。 天然ゴムに対する液状ポリイソプレンゴムの配
合量は前記のように天然ゴム100部に対して液状
のポリイソプレンゴム1〜7部の範囲であるが、
これは液状ポリイソプレンゴムの配合量が前記範
囲より少ない場合は混ざり易さ、分散性、抽出な
どの成形作業性を向上させる効果が少なく、逆に
前記範囲より多くなると加硫ゴムの物性を低下さ
せるからである。 本発明のテニスボールのコアー用組成物は、上
記のように天然ゴム100部に対して液状ポリイソ
プレンゴム1〜7部を配合し、さらに酸化亜鉛3
〜20部、炭酸カルシウム、炭酸マグネシウム、ケ
イ酸化合物、クレーなどの充填剤20〜60部、硫黄
2〜5部、促進剤(加硫促進剤)1〜5部を配合
し、要すればその他のゴム用配合剤を適宜配合す
ることによつて得られる。 本発明のテニスボールのコアー用組成物におい
て、基材ゴムとして天然ゴムを用いるのは、天然
ゴムが加工性および加硫特性が優れており、かつ
液状ポリイソプレンゴムとの相溶性が良いからで
ある。また、上記天然ゴムの特性を損なわない範
囲で、天然ゴムの一部をブタジエンゴム、エチレ
ンプロピレンジエンゴム、スチレンブタジエンゴ
ムなどで置き換えてもよい。また、酸化亜鉛、充
填剤、硫黄、促進剤などを上記割合で配合するの
は、それらをそのような割合で配合するのが適正
なコンプレツシヨンを得るのに適しているからで
ある。 本発明のゴム組成物よりテニスボール用のコア
ーを得るには、通常、ゴム組成物を半球殻状に成
形し、それを中空内にガス発生剤を詰めて2個貼
り合わせてボール状にし、加硫する。 つぎに実施例をあげて本発明を説明する。 実施例1〜2および比較例1〜3 第1表に示す組成のゴム組成物を調製し、その
ムーニー粘度および加硫後の物性を測定した。そ
の結果を第2表に示す。 なお混練は、硫黄、促進剤以外の配合剤とゴム
をバンバリーミキサーで混練し、硫黄および促進
剤はロールで上記混練物に加え混練した。加硫は
141℃で30分間加圧下で行なわれ、加硫ゴムの物
性測定はJIS K 6301に規定する試験方法に準じ
て行なわれた。
The present invention relates to a rubber composition for the core of a tennis ball. In general, rubber compositions require softeners to improve the mixability and dispersibility of compounding ingredients, improve rubber flow, and facilitate molding operations such as extraction and rolling. It contains higher fatty acids such as cotton oil, higher fatty acid esters such as castor oil, vegetable oil softeners such as pine tar and tall oil, and petroleum softeners such as spindle oil and process oil. In the rubber composition for the core, the above-mentioned softening agent has the disadvantage of increasing compression (that is, softening the core), which is an important characteristic of the core. Therefore, the amount of vulcanizing agent is increased to increase the degree of vulcanization and achieve proper compression. In this case, the durability and feel (hitting feeling) are reduced. In view of such circumstances, the present invention uses low molecular weight liquid polyisoprene rubber in place of conventional softeners to improve the processability of unvulcanized rubber (that is, to improve the ease of mixing of compounding agents and Improves dispersibility, improves rubber flow, improves molding workability such as extraction and rolling), and allows appropriate compression to be obtained without increasing the amount of vulcanizing agent. It is. That is, the present invention uses 100 parts of natural rubber (parts by weight,
1 to 7 parts of liquid polyisoprene rubber with an average molecular weight of 20,000 to 70,000, 3 to 20 parts of zinc oxide
A rubber composition for a tennis ball core, characterized in that it contains 20 to 60 parts of a filler, 2 to 5 parts of sulfur, and 1 to 5 parts of an accelerator. In the present invention, liquid polyisoprene rubber is used with the expectation that it will improve the processability of the rubber when unvulcanized, but this liquid polyisoprene rubber is compatible with conventional softeners that do not participate in crosslinking. Unlike softeners, they are vulcanized by a vulcanizing agent, and after vulcanization they themselves have some rubber-like elasticity, so unlike conventional softeners, they do not cause a large deterioration in rubber properties. It also has a good effect on improving the processability of unvulcanized rubber, and can be used satisfactorily as a softening agent. In the present invention, the liquid polyisoprene rubber used has an average molecular weight in the range of 20,000 to 70,000.
This is because those with an average molecular weight of less than 20,000 deteriorate the physical properties of the vulcanized rubber, while those with an average molecular weight of more than 70,000 have little effect on improving molding workability such as ease of mixing, dispersibility, and extraction. The amount of liquid polyisoprene rubber mixed with natural rubber is in the range of 1 to 7 parts of liquid polyisoprene rubber per 100 parts of natural rubber, as described above.
This is because if the amount of liquid polyisoprene rubber blended is less than the above range, it will have little effect on improving molding workability such as ease of mixing, dispersibility, and extraction, and conversely, if it exceeds the above range, the physical properties of the vulcanized rubber will deteriorate. This is because it makes you The composition for the core of a tennis ball of the present invention contains 1 to 7 parts of liquid polyisoprene rubber to 100 parts of natural rubber as described above, and further contains 3 parts of zinc oxide.
~20 parts, 20 to 60 parts of filler such as calcium carbonate, magnesium carbonate, silicate compound, clay, 2 to 5 parts of sulfur, 1 to 5 parts of accelerator (vulcanization accelerator), and other ingredients if necessary. It can be obtained by appropriately blending the following rubber compounding agents. In the tennis ball core composition of the present invention, natural rubber is used as the base rubber because natural rubber has excellent processability and vulcanization properties, and is also highly compatible with liquid polyisoprene rubber. be. Further, a part of the natural rubber may be replaced with butadiene rubber, ethylene propylene diene rubber, styrene butadiene rubber, etc., within a range that does not impair the properties of the natural rubber. Furthermore, the reason why zinc oxide, filler, sulfur, accelerator, etc. are blended in the above proportions is that blending them in such proportions is suitable for obtaining proper compression. In order to obtain a core for a tennis ball from the rubber composition of the present invention, the rubber composition is usually formed into a hemispherical shell shape, the hollow part is filled with a gas generating agent, and two pieces are bonded together to form a ball shape. Vulcanize. Next, the present invention will be explained with reference to Examples. Examples 1-2 and Comparative Examples 1-3 Rubber compositions having the compositions shown in Table 1 were prepared, and their Mooney viscosity and physical properties after vulcanization were measured. The results are shown in Table 2. For kneading, the rubber and compounding ingredients other than sulfur and the accelerator were kneaded using a Banbury mixer, and the sulfur and accelerator were added to the above-mentioned kneaded material using a roll and kneaded. Vulcanization is
The test was carried out under pressure at 141°C for 30 minutes, and the physical properties of the vulcanized rubber were measured according to the test method specified in JIS K 6301.

【表】【table】

【表】 ※2:ジベンゾチアジルジスルフイド
[Table] *2: Dibenzothiazyl disulfide

【表】 第2表に示すように、本発明の実施例1〜2の
組成物は軟化剤の配合しなかつた比較例3の組成
物に比べてムーニー粘度が低く、それによつて本
発明の実施例1〜2の組成物の混ざり易さ、分散
性、抽出特性などの成形作業性が良好であること
が明らかにされている。また本発明の実施例1〜
2の組成物は従来の軟化剤を配合した比較例1〜
2の組成物よりモジユラスが高く、コアー用ゴム
組成物として好適であることが明らかである。 つぎに前記実施例1〜2および比較例1〜2の
ゴム組成物によりテニスボール用のコアーを製造
し、その特性を測定した。その結果を第3表に示
す。なおコアーの製造はゴム組成物を半球殻状に
成形し、それを2個中空内にアンモニウム塩と亜
硝酸塩との混合物よりなるガス発生剤を充填して
球状になるように貼り合わせ、150℃で10分間加
圧下で加硫することによつて行なわれた。加硫後
のコアー(コアーボール)の外径は60.5mmであ
る。
[Table] As shown in Table 2, the compositions of Examples 1 and 2 of the present invention had a lower Mooney viscosity than the composition of Comparative Example 3, which did not contain a softener, and thereby It has been revealed that the compositions of Examples 1 and 2 have good molding workability such as ease of mixing, dispersibility, and extraction characteristics. Further, Examples 1 to 1 of the present invention
Compositions No. 2 are Comparative Examples 1 to 2, in which conventional softeners were blended.
It is clear that the modulus is higher than that of composition No. 2 and that it is suitable as a core rubber composition. Next, cores for tennis balls were manufactured using the rubber compositions of Examples 1 and 2 and Comparative Examples 1 and 2, and their properties were measured. The results are shown in Table 3. The core is manufactured by molding the rubber composition into a hemispherical shell shape, filling the hollow space with a gas generating agent made of a mixture of ammonium salt and nitrite, bonding them together to form a spherical shape, and heating at 150°C. This was done by vulcanization under pressure for 10 minutes. The outer diameter of the core (core ball) after vulcanization is 60.5 mm.

【表】 コンプレツシヨンは値が小さいほど腰の強い硬
いコアーボールをあらわすが、テニスボール用の
コアーとしては6.8±0.2の範囲が良好であると考
えられる。従つて目標値は6.8とされるが、本発
明の組成物は、実施例1および2とも上記範囲に
入り、コンプレツシヨン面からはテニスボールの
コアー用組成物として好ましいものであるといえ
る。すなわち、コンプレツシヨンが6.8±0.2の範
囲で良好な打球感が得られ、コンプレツシヨンが
上記範囲より小さくなると、硬く、衝撃の大きい
打球感となり、またコンプレツシヨンが上記範囲
より大きくなると、軟らかくなりすぎ、打球感が
悪くなると共に飛びが悪くなるが、実施例1の組
成物はコンプレツシヨンが6.80で、実施例2の組
成物はコンプレツシヨンが6.88であり、いずれも
6.8±0.2の範囲内に入つていて、テニスボールの
コアー用組成物として好ましいものであるといえ
る。 また反撥高さは174±3cmでテニスボール用の
コアーとして良好であると考えられ、目標値は
174cmにされているが、本発明の組成物は実例1、
2とも目標値に近く、この面からもテニスボール
のコアー用組成物として好ましいものであるとい
える。
[Table] A smaller compression value indicates a firmer core ball, but a range of 6.8±0.2 is considered to be good for a core for a tennis ball. Therefore, the target value is set at 6.8, and the compositions of the present invention fall within the above range in both Examples 1 and 2, and can be said to be preferable as compositions for tennis ball cores from the compression point of view. In other words, when the compression is within the range of 6.8±0.2, a good shot feel is obtained; when the compression is smaller than the above range, the ball feels hard and has a large impact; when the compression is larger than the above range, The composition of Example 1 had a compression of 6.80, and the composition of Example 2 had a compression of 6.88.
It falls within the range of 6.8±0.2, and can be said to be preferable as a composition for the core of a tennis ball. In addition, the repulsion height is 174±3cm, which is considered to be good as a core for tennis balls, and the target value is
174cm, but the composition of the present invention is Example 1,
Both values are close to the target values, and from this point of view, it can be said that the composition is preferable as a composition for the core of a tennis ball.

Claims (1)

【特許請求の範囲】[Claims] 1 天然ゴム100重量部に対して平均分子量20000
〜70000の液状ポリイソプレンゴム1〜7重量部、
酸化亜鉛3〜20重量部、充填剤20〜60重量部、硫
黄2〜5重量部および促進剤1〜5重量部を配合
したことを特徴とするテニスボールのコアー用ゴ
ム組成物。
1 Average molecular weight 20,000 per 100 parts by weight of natural rubber
~70000 liquid polyisoprene rubber 1 to 7 parts by weight,
A rubber composition for a tennis ball core, comprising 3 to 20 parts by weight of zinc oxide, 20 to 60 parts by weight of a filler, 2 to 5 parts by weight of sulfur, and 1 to 5 parts by weight of an accelerator.
JP465583A 1983-01-14 1983-01-14 Rubber composition for core of playing ball Granted JPS59129238A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP465583A JPS59129238A (en) 1983-01-14 1983-01-14 Rubber composition for core of playing ball

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP465583A JPS59129238A (en) 1983-01-14 1983-01-14 Rubber composition for core of playing ball

Publications (2)

Publication Number Publication Date
JPS59129238A JPS59129238A (en) 1984-07-25
JPH0350779B2 true JPH0350779B2 (en) 1991-08-02

Family

ID=11589956

Family Applications (1)

Application Number Title Priority Date Filing Date
JP465583A Granted JPS59129238A (en) 1983-01-14 1983-01-14 Rubber composition for core of playing ball

Country Status (1)

Country Link
JP (1) JPS59129238A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2727228B2 (en) * 1989-06-07 1998-03-11 横浜ゴム株式会社 Rubber composition for tire
CN106832442A (en) * 2016-11-29 2017-06-13 天长市良文运动器材有限公司 A kind of baseball core elastomeric material

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5152449A (en) * 1974-10-31 1976-05-10 Idemitsu Kosan Co SEIKEIYOGO MUSOSEIBUTSU
JPS5272742A (en) * 1975-12-16 1977-06-17 Yokohama Rubber Co Ltd:The Rubber composition
JPS547450A (en) * 1977-06-20 1979-01-20 Kuraray Co Ltd Production of rubber composition with high unvulcanized strength
JPS54139954A (en) * 1978-04-22 1979-10-30 Sumitomo Rubber Ind Rubber composition
JPS5632529A (en) * 1979-08-28 1981-04-02 Japan Synthetic Rubber Co Ltd Rubber composition

Also Published As

Publication number Publication date
JPS59129238A (en) 1984-07-25

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