JPH0352310B2 - - Google Patents
Info
- Publication number
- JPH0352310B2 JPH0352310B2 JP59099150A JP9915084A JPH0352310B2 JP H0352310 B2 JPH0352310 B2 JP H0352310B2 JP 59099150 A JP59099150 A JP 59099150A JP 9915084 A JP9915084 A JP 9915084A JP H0352310 B2 JPH0352310 B2 JP H0352310B2
- Authority
- JP
- Japan
- Prior art keywords
- inner layer
- piece solid
- solid core
- layer
- outer layer
- 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
Links
- 239000007787 solid Substances 0.000 claims description 50
- 239000000203 mixture Substances 0.000 claims description 13
- 238000000034 method Methods 0.000 claims description 9
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 229920005989 resin Polymers 0.000 claims description 4
- 239000011347 resin Substances 0.000 claims description 4
- 238000000748 compression moulding Methods 0.000 claims description 3
- 238000010438 heat treatment Methods 0.000 claims description 3
- 239000000126 substance Substances 0.000 claims description 3
- 230000006835 compression Effects 0.000 claims description 2
- 238000002347 injection Methods 0.000 claims description 2
- 239000007924 injection Substances 0.000 claims description 2
- 238000001746 injection moulding Methods 0.000 claims description 2
- 239000003431 cross linking reagent Substances 0.000 description 10
- 229920001971 elastomer Polymers 0.000 description 8
- 239000005060 rubber Substances 0.000 description 8
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 6
- 239000000853 adhesive Substances 0.000 description 5
- 230000001070 adhesive effect Effects 0.000 description 5
- 238000005259 measurement Methods 0.000 description 4
- XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 229920000554 ionomer Polymers 0.000 description 3
- 238000004898 kneading Methods 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000011787 zinc oxide Substances 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 244000043261 Hevea brasiliensis Species 0.000 description 2
- 239000005062 Polybutadiene Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- -1 butyl peroxide Chemical class 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- KRVSOGSZCMJSLX-UHFFFAOYSA-L chromic acid Substances O[Cr](O)(=O)=O KRVSOGSZCMJSLX-UHFFFAOYSA-L 0.000 description 2
- 150000001991 dicarboxylic acids Chemical class 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- AWJWCTOOIBYHON-UHFFFAOYSA-N furo[3,4-b]pyrazine-5,7-dione Chemical compound C1=CN=C2C(=O)OC(=O)C2=N1 AWJWCTOOIBYHON-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 150000002763 monocarboxylic acids Chemical class 0.000 description 2
- 229920003052 natural elastomer Polymers 0.000 description 2
- 229920001194 natural rubber Polymers 0.000 description 2
- 229920002857 polybutadiene Polymers 0.000 description 2
- 238000005488 sandblasting Methods 0.000 description 2
- 238000004381 surface treatment Methods 0.000 description 2
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 2
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- XKMZOFXGLBYJLS-UHFFFAOYSA-L zinc;prop-2-enoate Chemical compound [Zn+2].[O-]C(=O)C=C.[O-]C(=O)C=C XKMZOFXGLBYJLS-UHFFFAOYSA-L 0.000 description 2
- PAOHAQSLJSMLAT-UHFFFAOYSA-N 1-butylperoxybutane Chemical compound CCCCOOCCCC PAOHAQSLJSMLAT-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 229920003311 DuPont™ Surlyn® 1601 Polymers 0.000 description 1
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 229920003182 Surlyn® Polymers 0.000 description 1
- FMRLDPWIRHBCCC-UHFFFAOYSA-L Zinc carbonate Chemical compound [Zn+2].[O-]C([O-])=O FMRLDPWIRHBCCC-UHFFFAOYSA-L 0.000 description 1
- 238000004873 anchoring Methods 0.000 description 1
- 238000005422 blasting Methods 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 239000011243 crosslinked material Substances 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 239000011256 inorganic filler Substances 0.000 description 1
- 229910003475 inorganic filler Inorganic materials 0.000 description 1
- 159000000003 magnesium salts Chemical class 0.000 description 1
- 150000005673 monoalkenes Chemical class 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 238000009832 plasma treatment Methods 0.000 description 1
- 229920001084 poly(chloroprene) Polymers 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
- 239000011667 zinc carbonate Substances 0.000 description 1
- 229910000010 zinc carbonate Inorganic materials 0.000 description 1
- 235000004416 zinc carbonate Nutrition 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A63—SPORTS; GAMES; AMUSEMENTS
- A63B—APPARATUS FOR PHYSICAL TRAINING, GYMNASTICS, SWIMMING, CLIMBING, OR FENCING; BALL GAMES; TRAINING EQUIPMENT
- A63B37/00—Solid balls; Rigid hollow balls; Marbles
- A63B37/0003—Golf balls
- A63B37/007—Characteristics of the ball as a whole
- A63B37/0077—Physical properties
- A63B37/0097—Layers interlocking by means of protrusions or inserts, lattices or the like
Landscapes
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Physical Education & Sports Medicine (AREA)
Description
産業上の利用分野
本発明は改良されたスリーピースソリツドゴル
フボールおよびその製造方法に関する。
従来の技術
糸巻きゴルフボールの耐久性を改良するために
開発されたソリツドゴルフボールにおいては、反
撥性を高くすると耐久性が低下し、逆に耐久性を
高くすると反撥性が悪くなるという難点があるた
め、通常は比較的弾性に富むソリツドコアを比較
的耐久性に優れたカバーで被覆されたツーピース
ソリツドコアが使用されているが、十分満足すべ
きものはない。
発明が解決しようとする問題点
このような欠点を除去するためにソリツドコア
を反撥弾性に優れた内層と耐久性に優れた外層の
2層に分けたスリーピースソリツドゴルフボール
が開発されている。しかしながら、このようなス
リーピースソリツドゴルフボールにおいては、ソ
リツドコアの内層と外層を合体させるプレス加工
時において外層ゴムの偏肉が生じやすいために均
一な品質のボールが得難いばかりでなく、内層と
外層との間に十分な密着性を付与することが困難
なために比較的早期に割れたり、反撥特性が低下
するなど耐久性に関する難点を依然として払拭し
ていない。本発明はこのようなスリーピースソリ
ツドゴルフボールの欠点を解消するためになされ
たものである。
問題点を解決するための手段
即ち本発明は、第1図の模式的断面図に示すよ
うに、内層1と外層2から成るツーピースソリツ
ドコアをカバー3で被覆して成るスリーピースソ
リツドゴルフボールにおいて、内層1の表面上
に、外層2の厚さと同程度の高さを有して該内層
と一体成形された突起1′を設けたことを特徴と
するスリーピースソリツドゴルフボールおよびそ
の製造方法に関する。
本発明によるスリーピースソリツドゴルフボー
ルのコアを構成する内層1と外層2の配合組成は
同一にするのが一般的であるが、所望により適宜
変えてもよい。
ソリツドコアの配合成分には基材ゴム、架橋
剤、共架橋剤、不活性充填剤等が含まれる。
基材ゴムとしては従来からソリツドゴルフボー
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ができるが、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く、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
てもよい。
架橋剤としてはジクミルパーオキサイドやt−
ブチルパーオキサイドのような有機過酸化物等が
例示されるが、特に好ましいものはジクミルパー
オキサイドである。
架橋剤の配合量は基材ゴム100重量部に対して
通常0.5〜3.0重量部、好ましくは1.0〜2.5重量部
である。
共架橋剤としては特に限定するものではない
が、不飽和脂肪酸の金属塩、就中、炭素原子数3
〜8の不飽和脂肪酸(例えばアクリル酸、メタク
リル酸等)の亜鉛塩やマグネシウム塩が例示され
るが、アクリル酸亜鉛(正塩)が特に好適で、こ
の配合量は基材ゴム100重量部に対して20〜38重
量部、好ましくは25〜36重量部である。
不活性充填剤としては酸化亜鉛、硫酸バリウ
ム、シリカ、炭酸カルシウムおよび炭酸亜鉛等が
例示されるが、酸化亜鉛が一般的で、その配合量
は内層と外層の比重、ボールの重量規格等に左右
され、特に限定的ではないが、通常は基材ゴム
100重量部に対して3〜150重量部である。
上記成分を配合して得られるコア内層用組成物
は常套の混練機、例えばバンバリーミキサーやロ
ール等を用いて混練し、突起1′に対応する凹部
を備えたコア内層用金型に圧縮または射出成形
し、成形体を架橋剤および共架橋剤が作用するの
に十分な温度(例えば架橋剤としてジクミルパー
オキサイドを用い、共架橋剤としてアクリル酸亜
鉛を用いた場合には約150〜170℃)で加熱硬化さ
せて、表面に突起1′を有したソリツドコア内層
を調製する。
突起の形状、高さ、数、配設法等は特に限定的
ではないが、通常は例えば先端部を丸めた円柱状
突起(直径約2〜3mm;高さ約1〜3mm)をソリ
ツドコア内層表面上に6〜20個均等に配設させ
る。
突起を有したソリツドコア内層の表面は次いで
バフ処理および/または化学的処理に付す。
バフ処理は例えば、サンドブラスト、鉄粉ブラ
スト、振動バレル処理等によつておこなう。
また、化学的処理は例えば、塩素化合物(例え
ば塩素水等)、クロム酸等を約0.1〜5%の濃度で
用いておこなう。化学的処理をほどこした内層表
面は水洗後、乾燥させる。この他にプラズマ処理
等も挙げられる。
本発明によるスリーピースソリツドゴルフボー
ルのソリツドコアは上記のようにして調製された
内層上にさらに外層を設けることによつて形成さ
れる。即ち、前記成分を配合混練して得られるコ
ア外層用組成物をコア内層上に同中心的に金型内
圧縮または射出成形によつて設け、この2層成形
体を外層中に配合された架橋剤や共架橋剤が作用
するのに十分な温度で加熱硬化してツーピースソ
リツドコアとする。
この工程においては、内層1の表面上に外層2
とほぼ同程度の高さを有した突起1′が存在する
ために外層ゴムの偏肉が有効に防止され、また内
層表面の前記処理効果と突起1′のアンカー効果
とが相俟つて内層と外層の界面の接着性は接着剤
を使用しなくても著しく改善される。
以上のようにして得られるツーピースソリツド
コアは厚さ1.4〜2.7mmのカバーで被覆される。カ
バーとしてはアイオノマー樹脂を主材とし、必要
により着色等の目的で無機充填剤(例えば二酸化
チタン、酸化亜鉛等)を含有させたものが通常使
用される。
好ましいアイオノマー樹脂はモノオレフインと
炭素原子数3〜8の不飽和モノまたはジカルボン
酸およびそれらのエステルから成る群から選択さ
れる少なくとも1種との重合体(不飽和モノまた
はジカルボン酸および/またはこれらのエステル
4〜30重量%含有)に交差金属結合を付与した熱
可塑性樹脂である。このようなアイオノマー樹脂
としてはデユ・ポン社から市販されている各種の
「サーリン」(例えば、サーリン1601、1707、1605
等またはこれらの組合せ)が例示される。
カバーをソリツドコアに被覆する方法は特に限
定的ではないが、通常は予め半球殻状に成形した
2枚のカバーでソリツドコアを包み、加熱加圧成
形するが、カバー用組成物を射出成形してソリツ
ドコアを包みこんでもよい。
以下、本発明を実施例によつて説明する。
実施例
実施例 1
表−1の配合処方によるコア内層用組成物を混
練ロールを用いて混練し、これを、内部に深さ約
3mmの先端部を丸めた円柱状の凹部(12個;球面
を12面体に分割し、その個々の面に突起を1個づ
つ配列させる。)を均等に配列した直径31mmの球
状金型内において160℃で20分間加圧成形して表
面に突起を有したソリツドコア内層を調製した。
このコア内層の表面をサンドブラストを用いて
バフ処理し、次いでコア内層上に同中心的に、表
−1の配合処方により混練したコア外層用組成物
を圧縮成形によつて設け、この2層成形体を160
℃で20分間加熱処理してツーピースソリツドコア
を得た。
得られたツーピースソリツドコアを表−1の配
合処方によつて調製した2枚の半球殻状カバー
(厚さ約2.3mm)で包み、150℃で2分間加圧成形
して直径41.3mmのスリーピースソリツドゴルフボ
ールを製造した。
穴あけ機(8mmφ)を用いてこのボールのソリ
ツドコア内層まで打ち抜き、内層と外層との界面
を千枚通で剥離しようとしたところ、内層と外層
との接着が良好で剥離できず、無理に剥離しよう
としたところソリツドコアの材料破壊が生じた。
内層と外層のこの良好な密着性は、ボールを45
m/秒の速度で衝突板に100回打ちつけた後でも
損われなかつた。
また、ボールの初期の反撥係数およびボールを
45m/秒の速度で衝突板に100回打ちつけた後の
反撥係数をクラブヘツドスピード45m/秒のもと
で調べた。
さらに、ボールを45m/秒の速度で衝突板に繰
り返し打ちつけ、ボールが割れるまでの打撃回数
を求めた。
以上の測定結果を表−2に示す。
実施例 2
ソリツドコア内層表面処理をクロム酸の0.5%
溶液を用いておこなう以外は実施例1の手順を繰
り返し、測定結果を表−2に示す。
なお、ソリツドコアの内層と外層の密着性は実
施例1の場合と同様に極めて良好なものであつ
た。
比較例 1
表面処理をほどこさず、かつ突起を設けないソ
リツドコア内層を使用する以外は実施例1と同様
の手順を繰り返し、測定結果を表−2に示す。
この場合のソリツドコアの内層と外層との密着
性は全くなく、コアを真二つに切断すると外層が
はずれてしまつた。又、外観の厚みについて最大
最小差を調べた所1.2m/mもあつた。
比較例 2
ソリツドコアの内層と外層とを接着剤(ネオプ
レン系接着剤)を用いて接着させる以外は比較例
1の手順を繰り返し、測定結果を表−2に示す。
なお、この場合のソリツドコアの内層と外層と
の密着性は比較的良好であつたが、ボールの反撥
弾性は低下した。
FIELD OF THE INVENTION This invention relates to an improved three-piece solid golf ball and method of manufacturing the same. Conventional technology Solid golf balls developed to improve the durability of thread-wound golf balls have the disadvantage that increasing repulsion reduces durability, and conversely, increasing durability deteriorates repulsion. Therefore, a two-piece solid core is usually used in which a relatively elastic solid core is covered with a relatively durable cover, but none of them are fully satisfactory. Problems to be Solved by the Invention In order to eliminate these drawbacks, a three-piece solid golf ball has been developed in which the solid core is divided into two layers: an inner layer with excellent rebound and an outer layer with excellent durability. However, in such a three-piece solid golf ball, it is not only difficult to obtain a ball of uniform quality because uneven thickness of the outer rubber layer tends to occur during the press process that combines the inner and outer layers of the solid core, but also the inner and outer layers are Difficulties regarding durability, such as relatively early cracking and deterioration of repulsion properties due to the difficulty of imparting sufficient adhesion between the materials, have not yet been overcome. The present invention has been made to overcome the drawbacks of such three-piece solid golf balls. Means for Solving the Problems According to the present invention, as shown in the schematic cross-sectional view of FIG. A three-piece solid golf ball and a method for manufacturing the same, characterized in that a protrusion 1' having a height comparable to the thickness of the outer layer 2 and integrally formed with the inner layer 1 is provided on the surface of the inner layer 1, and a method for manufacturing the same. Regarding. Although the compositions of the inner layer 1 and the outer layer 2 constituting the core of the three-piece solid golf ball according to the present invention are generally the same, they may be changed as desired. The components of the solid core include a base rubber, a crosslinking agent, a co-crosslinking agent, an inert filler, and the like. As the base rubber, any 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 is particularly preferred, and if desired, natural rubber, polyisoprene rubber, styrene-butadiene rubber, etc. may be appropriately blended with the polybutadiene. Dicumyl peroxide and t-
Examples include organic peroxides such as butyl peroxide, but dicumyl peroxide is particularly preferred. The amount of the crosslinking agent blended is usually 0.5 to 3.0 parts by weight, preferably 1.0 to 2.5 parts by weight, based on 100 parts by weight of the base rubber. The co-crosslinking agent is not particularly limited, but includes metal salts of unsaturated fatty acids, especially metal salts having 3 carbon atoms.
Examples include zinc salts and magnesium salts of unsaturated fatty acids (e.g. acrylic acid, methacrylic acid, etc.) of 8 to 8, but zinc acrylate (normal salt) is particularly preferred, and the amount is based on 100 parts by weight of the base rubber. 20 to 38 parts by weight, preferably 25 to 36 parts by weight. Examples of inert fillers include zinc oxide, barium sulfate, silica, calcium carbonate, and zinc carbonate, but zinc oxide is common, and its amount depends on the specific gravity of the inner and outer layers, the weight standard of the ball, etc. Usually, but not exclusively, the base rubber
The amount is 3 to 150 parts by weight per 100 parts by weight. The core inner layer composition obtained by blending the above components is kneaded using a conventional kneading machine, such as a Banbury mixer or a roll, and then compressed or injected into a core inner layer mold having recesses corresponding to the protrusions 1'. The temperature is sufficient for the crosslinking agent and co-crosslinking agent to act (for example, approximately 150 to 170°C when dicumyl peroxide is used as the crosslinking agent and zinc acrylate is used as the co-crosslinking agent). ) to prepare a solid core inner layer having protrusions 1' on the surface. The shape, height, number, arrangement method, etc. of the protrusions are not particularly limited, but usually, for example, cylindrical protrusions with rounded tips (about 2 to 3 mm in diameter; about 1 to 3 mm in height) are placed on the inner layer surface of the solid core. Arrange 6 to 20 pieces evenly. The surface of the solid core inner layer with protrusions is then subjected to buffing and/or chemical treatment. The buffing treatment is performed by, for example, sandblasting, iron powder blasting, vibrating barrel treatment, or the like. Further, the chemical treatment is performed using, for example, a chlorine compound (for example, chlorine water, etc.), chromic acid, etc. at a concentration of about 0.1 to 5%. The chemically treated inner layer surface is washed with water and then dried. Other examples include plasma treatment. The solid core of the three-piece solid golf ball according to the present invention is formed by further providing an outer layer on the inner layer prepared as described above. That is, a core outer layer composition obtained by blending and kneading the above components is provided concentrically on the core inner layer by in-mold compression or injection molding, and this two-layer molded body is then mixed with the crosslinked material contained in the outer layer. A two-piece solid core is formed by heating and curing at a temperature sufficient for the action of the crosslinking agent and co-crosslinking agent. In this step, the outer layer 2 is placed on the surface of the inner layer 1.
Due to the presence of the protrusions 1' having almost the same height as the inner layer, uneven thickness of the outer layer rubber is effectively prevented, and the effect of the treatment on the surface of the inner layer and the anchoring effect of the protrusions 1' combine to prevent the inner layer from becoming uneven. The interfacial adhesion of the outer layer is significantly improved without the use of adhesives. The two-piece solid core obtained as described above is covered with a cover having a thickness of 1.4 to 2.7 mm. The cover is usually made of an ionomer resin and contains an inorganic filler (for example, titanium dioxide, zinc oxide, etc.) for the purpose of coloring, if necessary. A preferred ionomer resin is a polymer of a monoolefin and at least one member selected from the group consisting of unsaturated mono- or dicarboxylic acids having 3 to 8 carbon atoms and esters thereof (unsaturated mono- or dicarboxylic acids and/or esters thereof). It is a thermoplastic resin with cross-metal bonds added to (contains 4 to 30% by weight of ester). Such ionomer resins include various "Surlyn" commercially available from DuPont (for example, Surlyn 1601, 1707, 1605).
etc. or a combination thereof). The method of coating the solid core with the cover is not particularly limited, but usually the solid core is wrapped with two covers formed in advance into a hemispherical shell shape and molded under heat and pressure, but the cover composition is injection molded to form the solid core. You can also wrap it around. Hereinafter, the present invention will be explained with reference to Examples. Examples Example 1 The core inner layer composition according to the formulation shown in Table 1 was kneaded using a kneading roll, and the core inner layer composition was mixed into cylindrical recesses (12; spherical was divided into dodecahedrons, and one protrusion was arranged on each face.) was pressure-molded at 160°C for 20 minutes in a spherical mold with a diameter of 31 mm in which the protrusions were arranged evenly to form protrusions on the surface. A solid core inner layer was prepared. The surface of this core inner layer is buffed using sandblasting, and then a core outer layer composition kneaded according to the formulation shown in Table 1 is applied concentrically on the core inner layer by compression molding, and this two-layer molding is performed. body 160
A two-piece solid core was obtained by heat treatment at ℃ for 20 minutes. The obtained two-piece solid core was wrapped with two hemispherical shell-like covers (approximately 2.3 mm thick) prepared according to the formulation shown in Table 1, and pressure molded at 150°C for 2 minutes to form a 41.3 mm diameter solid core. A three-piece solid golf ball was manufactured. I punched out the inner layer of the solid core of this ball using a hole puncher (8mmφ) and tried to peel off the interface between the inner and outer layers with an awl, but the adhesion between the inner and outer layers was good and I could not peel it off, so I tried to force it. As a result, material failure of the solid core occurred.
This good adhesion between the inner and outer layers makes the ball 45
It remained undamaged even after hitting the impact plate 100 times at a speed of m/s. Also, the initial coefficient of repulsion of the ball and the ball
The repulsion coefficient after hitting the impact plate 100 times at a speed of 45 m/sec was examined at a club head speed of 45 m/sec. Furthermore, the ball was repeatedly hit against the collision plate at a speed of 45 m/sec, and the number of hits until the ball cracked was determined. The above measurement results are shown in Table-2. Example 2 Solid core inner layer surface treatment with 0.5% chromic acid
The procedure of Example 1 was repeated except that a solution was used, and the measurement results are shown in Table 2. Note that, as in Example 1, the adhesion between the inner layer and the outer layer of the solid core was extremely good. Comparative Example 1 The same procedure as in Example 1 was repeated except that a solid core inner layer without surface treatment and without protrusions was used, and the measurement results are shown in Table 2. In this case, there was no adhesion between the inner layer and the outer layer of the solid core, and when the core was cut into two, the outer layer came off. Also, when we investigated the maximum and minimum difference in external thickness, we found that it was 1.2m/m. Comparative Example 2 The procedure of Comparative Example 1 was repeated except that the inner layer and outer layer of the solid core were bonded together using an adhesive (neoprene adhesive), and the measurement results are shown in Table 2. In this case, although the adhesion between the inner layer and the outer layer of the solid core was relatively good, the rebound resilience of the ball was reduced.
【表】【table】
【表】
発明の効果
本発明に係わるスリーピースソリツドゴルフボ
ールは、従来の同種製品において不十分であつた
ソリツドコアの内層と外層との密着性を接着剤を
使用せずに改良すると共に、外層ゴムの偏肉のな
い均一なソリツドゴルフボールであり、従来品に
比べて同等またはそれ以上の反撥特性を保持しつ
つ改良された耐久性を示し、また、打撃時のフイ
ーリングも極めて良好である。[Table] Effects of the Invention The three-piece solid golf ball according to the present invention improves the adhesion between the inner layer and the outer layer of the solid core, which was insufficient in conventional similar products, without using an adhesive, and also improves the adhesion between the inner layer and the outer layer of the solid core, which was insufficient in conventional similar products, and also improves the adhesion between the inner layer and the outer layer of the solid core without using an adhesive. It is a uniform solid golf ball with no uneven thickness, exhibits improved durability while maintaining the same or better repulsion characteristics than conventional products, and also has an extremely good feel when hit.
第1図は本発明によるスリーピースソリツドゴ
ルフボールの一態様を示す模式的断面図である。
1はソリツドコア内層、1′は突起、2はソリ
ツドコア外層、3はカバーを示す。
FIG. 1 is a schematic cross-sectional view showing one embodiment of a three-piece solid golf ball according to the present invention. 1 is an inner layer of the solid core, 1' is a protrusion, 2 is an outer layer of the solid core, and 3 is a cover.
Claims (1)
コアをカバー3で被覆して成るスリーピースソリ
ツドゴルフボールにおいて、内層1の表面上に、
外層2の厚さと同程度の高さを有して該内層と一
体成形された突起1′を設けたことを特徴とする
スリーピースソリツドゴルフボール。 2 カバーがアイオマー樹脂を主材とするカバー
である第1項記載のスリーピースソリツドゴルフ
ボール。 3 突起1′に対応する凹部を備えた球状金型内
で内層用組成物を圧縮または射出成形させた内層
1の表面をバフ処理および/または化学的処理に
付し、該内層上に外層用組成物を同中心的に球状
金型内で圧縮または射出成形させることによつて
外層2を設け、この2層成形体を加熱硬化して得
られるツーピースソリツドコアをカバーで被覆す
ることを特徴とするスリーピースソリツドゴルフ
ボールの製造方法。[Claims] 1. A three-piece solid golf ball comprising a two-piece solid core consisting of an inner layer 1 and an outer layer 2 and covered with a cover 3, in which on the surface of the inner layer 1,
A three-piece solid golf ball characterized in that a protrusion 1' having a height comparable to the thickness of the outer layer 2 and integrally formed with the inner layer is provided. 2. The three-piece solid golf ball according to item 1, wherein the cover is mainly made of iomer resin. 3. The surface of the inner layer 1, in which the composition for the inner layer is compressed or injection molded in a spherical mold having recesses corresponding to the protrusions 1', is subjected to buffing and/or chemical treatment, and the composition for the outer layer is applied on the inner layer. The outer layer 2 is provided by compression or injection molding the composition concentrically in a spherical mold, and the two-piece solid core obtained by heating and curing this two-layer molded product is covered with a cover. A method for manufacturing a three-piece solid golf ball.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59099150A JPS60241463A (en) | 1984-05-16 | 1984-05-16 | Three-piece golf ball |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59099150A JPS60241463A (en) | 1984-05-16 | 1984-05-16 | Three-piece golf ball |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS60241463A JPS60241463A (en) | 1985-11-30 |
JPH0352310B2 true JPH0352310B2 (en) | 1991-08-09 |
Family
ID=14239657
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP59099150A Granted JPS60241463A (en) | 1984-05-16 | 1984-05-16 | Three-piece golf ball |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS60241463A (en) |
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US6056842A (en) * | 1997-10-03 | 2000-05-02 | Acushnet Company | Method of making a golf ball with a multi-layer core |
US6093357A (en) * | 1998-03-26 | 2000-07-25 | Acushnet Company | Methods for making multi-layer golf balls using rigid uncrosslinked shells |
US6180722B1 (en) | 1998-03-26 | 2001-01-30 | Acushnet Company | Dual core golf ball compositions |
US6417278B1 (en) | 1998-03-26 | 2002-07-09 | Acushnet Company | Low compression, resilient golf balls including a cis-to-trans catalyst and method for making same |
US6290797B1 (en) | 1999-04-02 | 2001-09-18 | Acushnet Company | Process for making multi-layer core golf balls |
KR20020007836A (en) * | 2000-07-19 | 2002-01-29 | 신덕호 | Golf ball |
US6710114B2 (en) | 2000-12-21 | 2004-03-23 | Acushnet Company | Golf balls including solution blended polymeric composite and method of making same |
US6555627B2 (en) | 2000-12-21 | 2003-04-29 | Acushnet Company | Golf balls including rigid compositions and methods for making same |
US6955613B2 (en) | 2003-01-10 | 2005-10-18 | Mizuno Corporation | Multi-piece golf ball and manufacturing method thereof |
CN100382864C (en) | 2003-03-31 | 2008-04-23 | 美津浓株式会社 | Multi-piece golf ball, method of manufacturing the same, and molding die used for manufacturing the same |
JP2005052302A (en) | 2003-08-01 | 2005-03-03 | Norikazu Ninomiya | Golf ball and mold for molding its core |
WO2005089883A1 (en) | 2004-03-19 | 2005-09-29 | Mizuno Corporation | Multi-piece golf ball and method for manufacturing same |
JP4419026B2 (en) | 2004-06-09 | 2010-02-24 | 美津濃株式会社 | Multi-piece golf ball and manufacturing method thereof |
US7264560B2 (en) * | 2005-03-10 | 2007-09-04 | Callaway Golf Company | Golf ball |
US8979675B2 (en) * | 2012-04-25 | 2015-03-17 | Nike, Inc. | Golf ball core having radial appendages |
US9492716B2 (en) | 2013-07-05 | 2016-11-15 | Nike, Inc. | Multi-layer golf ball |
US20150011332A1 (en) * | 2013-07-05 | 2015-01-08 | Nike, Inc. | Multi-layer golf ball |
US9586096B2 (en) | 2013-07-05 | 2017-03-07 | Nike, Inc. | Multi-layer golf ball |
US9468814B2 (en) | 2013-07-05 | 2016-10-18 | Nike, Inc. | Multi-layer golf ball |
US10155137B2 (en) | 2013-07-05 | 2018-12-18 | Feng Tay Enterprises Co., Ltd | Golf ball core |
US9573023B2 (en) | 2013-07-05 | 2017-02-21 | Nike, Inc. | Multi-layer golf ball |
US9283440B2 (en) | 2013-11-08 | 2016-03-15 | Nike, Inc. | Multi-layer golf ball |
US9289656B2 (en) | 2013-11-21 | 2016-03-22 | Nike, Inc. | Multi-layer golf ball |
-
1984
- 1984-05-16 JP JP59099150A patent/JPS60241463A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS60241463A (en) | 1985-11-30 |
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