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JPS5929267B2 - solid golf ball - Google Patents
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JPS5929267B2 - solid golf ball - Google Patents

solid golf ball

Info

Publication number
JPS5929267B2
JPS5929267B2 JP55058405A JP5840580A JPS5929267B2 JP S5929267 B2 JPS5929267 B2 JP S5929267B2 JP 55058405 A JP55058405 A JP 55058405A JP 5840580 A JP5840580 A JP 5840580A JP S5929267 B2 JPS5929267 B2 JP S5929267B2
Authority
JP
Japan
Prior art keywords
weight
solid golf
parts
golf ball
bzm
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
Application number
JP55058405A
Other languages
Japanese (ja)
Other versions
JPS56156173A (en
Inventor
幹生 山田
一郎 富永
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 JP55058405A priority Critical patent/JPS5929267B2/en
Publication of JPS56156173A publication Critical patent/JPS56156173A/en
Publication of JPS5929267B2 publication Critical patent/JPS5929267B2/en
Expired legal-status Critical Current

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  • Compositions Of Macromolecular Compounds (AREA)
  • Graft Or Block Polymers (AREA)

Description

【発明の詳細な説明】 本発明はソリッドゴルフボールの改良に関する。[Detailed description of the invention] The present invention relates to improvements in solid golf balls.

ソリッドゴルフポールは、一体成形できるため一般にコ
スト的には有利であるが、糸巻きゴルフボールに比べて
反撥特性、スピン性能、フィーリング(打撃感触)等の
点で劣る。特に反撥特性はボールの初速度に大きな影響
を及ぼし、延いては飛距離を左右する重要な要因である
。従来から比較的良好な反撥特性を有するものとして常
用されているソリッドゴルフボールは基材ゴムに不活性
充填材や有機過酸化物の他に共架橋剤として塩丼性メタ
クリル酸亜鉛(BZM)を配合した組成物を加熱硬化し
て得られるものである。
Solid golf poles are generally advantageous in terms of cost because they can be integrally molded, but they are inferior to thread-wound golf balls in terms of repulsion characteristics, spin performance, feel (hit feel), and the like. In particular, repulsion characteristics have a large effect on the initial velocity of the ball, and are therefore an important factor that influences flight distance. Solid golf balls, which have traditionally been commonly used as having relatively good repulsion properties, contain salt-based zinc methacrylate (BZM) as a co-crosslinking agent in addition to inert fillers and organic peroxides in the base rubber. It is obtained by heating and curing the blended composition.

本発明者はBZMを加熱前処理することによつて、従来
のこのようなソリッドゴルフポールよわもエネルギー損
失が少な<、しかも糸巻きゴルフボールに匹敵し得る高
反撥弾性を有するソリッドゴルフポールが得られること
を充明し本発明を完成した。即ち本発明は基材ゴム10
0重量部、予め150〜200℃で加熱処理した塩基性
メタクリル酸亜鉛10〜60重量部、不活性充填剤20
〜80重量部、および有機過酸化物005〜5.0重量
部から成る組成物を加熱硬化成形して得られるソリッド
ゴルフポールに関する。
By pre-heating BZM, the present inventors have discovered that a solid golf pole can be obtained which has less energy loss than conventional solid golf poles and also has high repulsion comparable to that of thread-wound golf balls. The present invention was completed by fully clarifying the above. That is, the present invention is based on the base rubber 10.
0 parts by weight, 10 to 60 parts by weight of basic zinc methacrylate preheated at 150 to 200°C, and 20 parts by weight of inert filler.
The present invention relates to a solid golf pole obtained by heat-curing and molding a composition consisting of ~80 parts by weight and 0.05 to 5.0 parts by weight of an organic peroxide.

本発明の特徴は上述のようにBZMを加熱前処理するこ
とである。
A feature of the present invention is that BZM is preheated as described above.

BZMは酸化亜鉛とメタクリル酸を通常約1〜1.5:
lのモル比で反応させて得られる化合物で第1図のよ
うな減量曲線1および示差熱分析曲線2を与える。一方
、加熱による水分率の変化を測定すると130℃で約0
03重量%、180℃で約4.5重量%の水分がそれぞ
れ検出されたことから第1図における約150℃前後の
重量変化は結晶水の脱離によるものと考えられるが(結
晶水の脱離によるBZMの結晶構造変化は第2図のX線
回折パターンによつても支持される)、約20OOC以
上の変化は明らかにBZMの分解を示すものである。B
ZMを150゜Cl■)、下で前処理しても本発明によ
る効果は十分得られず、また200OC以上で前処理す
ると共架橋剤として作用しない。このようなことから、
本発明におけるBZMの前処理濃度は150〜200℃
であφ。、、前処理時間は通常1〜3時間である。
BZM usually contains zinc oxide and methacrylic acid in a ratio of about 1 to 1.5:
The compound obtained by reacting at a molar ratio of 1 to 1 gives a weight loss curve 1 and a differential thermal analysis curve 2 as shown in FIG. On the other hand, when measuring the change in moisture content due to heating, it is approximately 0 at 130℃.
Since water content of approximately 4.5% by weight was detected at 0.03% by weight and at 180°C, it is thought that the weight change around 150°C in Fig. 1 is due to the desorption of crystal water. The change in crystal structure of BZM due to separation is also supported by the X-ray diffraction pattern shown in FIG. 2), and a change of about 20 OOC or more clearly indicates decomposition of BZM. B
Even if ZM is pretreated at a temperature below 150°C (Cl), the effect of the present invention cannot be sufficiently obtained, and if ZM is pretreated at a temperature above 200OC, it does not act as a co-crosslinking agent. From such a thing,
The pretreatment concentration of BZM in the present invention is 150 to 200°C
Deφ. The pretreatment time is usually 1 to 3 hours.

このようにして得られるBZMは基材ゴム、不活性充填
剤および有機過酸化物と配合し、所定の温度例えば15
0−160℃p型内で一体成形してソリッドゴルフボー
ルとする。
The BZM thus obtained is blended with a base rubber, an inert filler and an organic peroxide and heated to a predetermined temperature, e.g.
A solid golf ball is formed by integral molding in a p-type mold at 0-160°C.

加熱前処理したBZMの配合量は基材ゴム100重量部
に対して通常10〜60重量部、好ましくは40〜60
重量部であわ、配合量がこれよりも少ないと所望の硬度
は得られず、多過ぎると硬度が高<な杉すぎてボールの
初速度も小さくなる。
The amount of BZM that has been preheated is usually 10 to 60 parts by weight, preferably 40 to 60 parts by weight, based on 100 parts by weight of the base rubber.
If the amount is less than this, the desired hardness will not be obtained, and if it is too much, the hardness will be too high and the initial speed of the ball will be low.

基材ゴムとしては従来からソリッドゴルフボールに用い
られている適宜の天然ゴムおよび/または合成ゴムを使
用することもできるが、本発明においては、シス構造を
少なくとも40%以上有する1,4−ポリブタジエンが
特に好まし<、所望により該ポリブタジエンに天然ゴム
、ポリイソプレンゴム、スチレンブタジエンゴム等を適
宜配合して使用してもよい。不活性充填材としてはZn
O.BaSO4、SiO2、CacO3、ZnCOs等
が例示されるが、ZnOが一般的で、これを基材ゴム1
00重量部に対して20〜80重量部配合する。
As the base rubber, suitable natural rubber and/or synthetic rubber that has been conventionally used in solid golf balls can be used, but in the present invention, 1,4-polybutadiene having at least 40% or more cis structure is used. It is particularly preferred that natural rubber, polyisoprene rubber, styrene-butadiene rubber, etc. may be blended with the polybutadiene as desired. Zn as an inert filler
O. Examples include BaSO4, SiO2, CacO3, ZnCOs, etc., but ZnO is common and is used as base rubber 1.
20 to 80 parts by weight per 00 parts by weight.

有機過酸化物としてはジクルミパーオキサイド、tーブ
チルパーオキシベンゾエート等を用いればよ<、これを
基材ゴム100重量部に対して0。
As the organic peroxide, diwalnut peroxide, t-butyl peroxybenzoate, etc. may be used in an amount of 0 per 100 parts by weight of the base rubber.

5〜5.0重量部配合する。Add 5 to 5.0 parts by weight.

本発明によるソリッドゴルフボールは従来のものと同等
の耐久性を保持しつつ、糸巻きゴルフボールに匹敵しう
る反撥特性を具えたものである。
The solid golf ball according to the present invention has repulsion characteristics comparable to those of thread-wound golf balls while maintaining durability equivalent to conventional golf balls.

以下、本発明を実施例および比較例によつて説明する。
実施例および比較例 表−1の配合比による3種類の組成物をロール混練ヤに
よつて調製した。
The present invention will be explained below using Examples and Comparative Examples.
EXAMPLES AND COMPARATIVE EXAMPLES Three types of compositions having the compounding ratios shown in Table 1 were prepared using a roll kneader.

1)日本合成ゴム株氏会社製ポリブタ仁ンコユ2)13
0℃で5時間処理したBZM3)160℃で3時間処理
したBZM 得られた組成物1,2および3を所定の型内で150℃
30分間加圧成形してそれぞれ直径1.62インチの一
体成形したソリソドゴルフボールI,■および■を調製
した。
1) Polybutanine made by Japan Synthetic Rubber Co., Ltd. 2) 13
BZM treated at 0°C for 5 hours 3) BZM treated at 160°C for 3 hours The obtained compositions 1, 2 and 3 were heated at 150°C in a predetermined mold.
Molded solid golf balls I, ■, and ■, each having a diameter of 1.62 inches, were prepared by pressure molding for 30 minutes.

ゴルフボールI,■および■についてコンプレッション
、初速度、および耐久性を試験した。
Golf balls I, ■, and ■ were tested for compression, initial velocity, and durability.

結果を表−2に示す。参考例 ’ 表−3の配合比による2種類の組成物をロール混練わに
よつて調製した。
The results are shown in Table-2. Reference Example 'Two types of compositions having the compounding ratios shown in Table 3 were prepared by roll kneading.

上記組成物を160℃で30分間ブレスして得られた厚
さ約0。
The thickness obtained by pressing the above composition at 160°C for 30 minutes was about 0.

6篤贋のスラブから4mm×40關×0。6. 4mm x 40cm x 0 from a fake slab.

6mmの大きさの試料片を切取つた。A sample piece with a size of 6 mm was cut out.

試料片の損失正接Tanδを粘弾性スペクトロメーター
(岩本製作所製)を用いて35℃、10Hzで測定した
The loss tangent Tan δ of the sample piece was measured at 35° C. and 10 Hz using a viscoelastic spectrometer (manufactured by Iwamoto Seisakusho).

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

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

第1図はBZMの減量曲線および示差熱分析曲線を表わ
す(キャリアーガスニN23Oゴ/Min、感度:±1
〜、加熱速度:10℃/Min、チヤートスピードニ1
0m[分In)サーモカツプルニCA,DTGレンジニ
l〜Amln)。 第2図はBZMOx線回折パターンを表わす。第3図は
エラストマーの動歪(横軸:%)と損失正接(縦軸:T
anδ)5との関係を表わす。1は減量曲線、2は示差
熱分析曲線、3は加熱処理BZM(7)X線回折パター
ン、4は未処理BZMのX線回折パターン、5は未処理
BZMを共架橋剤としたエラストマーの動歪と損失正接
との関係、6は加熱前処理BZMを共架橋剤としたエラ
ストマーの動歪と損失正接との関係を示す。
Figure 1 shows the weight loss curve and differential thermal analysis curve of BZM (carrier gas NiN23O/Min, sensitivity: ±1
~, heating rate: 10°C/Min, Chart Speedni 1
0 m [minutes In) Thermo Katsupuruni CA, DTG Rangeini I~Amln). FIG. 2 represents the BZMO x-ray diffraction pattern. Figure 3 shows the dynamic strain (horizontal axis: %) and loss tangent (vertical axis: T) of the elastomer.
and (δ)5. 1 is a weight loss curve, 2 is a differential thermal analysis curve, 3 is an X-ray diffraction pattern of heat-treated BZM (7), 4 is an X-ray diffraction pattern of untreated BZM, and 5 is the dynamic behavior of an elastomer using untreated BZM as a co-crosslinking agent. 6 shows the relationship between dynamic strain and loss tangent of an elastomer using heat-pretreated BZM as a co-crosslinking agent.

Claims (1)

【特許請求の範囲】 1 基材ゴム100重量部、予め150〜200℃で加
熱処理した塩基性メタクリル酸亜鉛10〜60重量部、
不活性充填剤20〜80重量部、および有機過酸化物0
.5〜5.0重量部から成る組成物を加熱硬化成形して
得られるソリッドゴルフボール。 2 基材ゴムがシス構造を少なくとも40%以上有する
1,4−ポリブタジエンである第1項記載のソリッドゴ
ルフボール。 3 不活性充填剤が酸化亜鉛である第1項記載のソリッ
ドゴルフボール。 4 有機過酸化物がジクミルパーオキサイドである第1
項記載のソリッドゴルフボール。
[Scope of Claims] 1. 100 parts by weight of base rubber, 10 to 60 parts by weight of basic zinc methacrylate preheated at 150 to 200°C,
20-80 parts by weight of inert filler and 0 organic peroxides
.. A solid golf ball obtained by thermosetting and molding a composition comprising 5 to 5.0 parts by weight. 2. The solid golf ball according to item 1, wherein the base rubber is 1,4-polybutadiene having at least 40% cis structure. 3. The solid golf ball of item 1, wherein the inert filler is zinc oxide. 4 The first organic peroxide is dicumyl peroxide
The solid golf ball described in Section 1.
JP55058405A 1980-04-30 1980-04-30 solid golf ball Expired JPS5929267B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP55058405A JPS5929267B2 (en) 1980-04-30 1980-04-30 solid golf ball

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP55058405A JPS5929267B2 (en) 1980-04-30 1980-04-30 solid golf ball

Publications (2)

Publication Number Publication Date
JPS56156173A JPS56156173A (en) 1981-12-02
JPS5929267B2 true JPS5929267B2 (en) 1984-07-19

Family

ID=13083446

Family Applications (1)

Application Number Title Priority Date Filing Date
JP55058405A Expired JPS5929267B2 (en) 1980-04-30 1980-04-30 solid golf ball

Country Status (1)

Country Link
JP (1) JPS5929267B2 (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5937961A (en) * 1982-08-17 1984-03-01 住友ゴム工業株式会社 Two-piece solid golf ball
JPS63265938A (en) * 1987-04-24 1988-11-02 Kinugawa Rubber Ind Co Ltd Rubber composition
JP6464651B2 (en) * 2013-10-17 2019-02-06 ブリヂストンスポーツ株式会社 Golf ball

Also Published As

Publication number Publication date
JPS56156173A (en) 1981-12-02

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