TWM556619U - Golf ball structure - Google Patents

Golf ball structure Download PDF

Info

Publication number
TWM556619U
TWM556619U TW106216040U TW106216040U TWM556619U TW M556619 U TWM556619 U TW M556619U TW 106216040 U TW106216040 U TW 106216040U TW 106216040 U TW106216040 U TW 106216040U TW M556619 U TWM556619 U TW M556619U
Authority
TW
Taiwan
Prior art keywords
composition
polyurethane
chain extender
golf ball
polyisocyanate
Prior art date
Application number
TW106216040U
Other languages
Chinese (zh)
Inventor
His-Chou Huang
Ming-Yen Huang
Original Assignee
Scanna 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 Scanna Co Ltd filed Critical Scanna Co Ltd
Priority to TW106216040U priority Critical patent/TWM556619U/en
Publication of TWM556619U publication Critical patent/TWM556619U/en

Links

Landscapes

  • Compositions Of Macromolecular Compounds (AREA)
  • Polyurethanes Or Polyureas (AREA)

Abstract

本創作揭露一種高爾夫球結構,其包含球心內層以及包圍球心內層且包含熱塑性聚氨酯組合物的外層。熱塑性聚氨酯組合物包含:由第一多異氰酸酯、第一多元醇組合物以及第一擴鏈劑組合物所組成的第一聚氨酯;由第二多異氰酸酯、第二多元醇組合物以及第二擴鏈劑組合物所組成的第二聚氨酯;以及由第三多異氰酸酯、第三多元醇組合物以及第三擴鏈劑組合物所組成的第三聚氨酯。The present disclosure discloses a golf ball structure comprising an inner core layer and an outer layer surrounding the inner core layer and comprising a thermoplastic polyurethane composition. The thermoplastic polyurethane composition comprises: a first polyurethane composed of a first polyisocyanate, a first polyol composition, and a first chain extender composition; a second polyisocyanate, a second polyol composition, and a second a second polyurethane composed of a chain extender composition; and a third polyurethane composed of a third polyisocyanate, a third polyol composition, and a third chain extender composition.

Description

高爾夫球結構Golf structure

本創作關於一種高爾夫球結構,特別是關於一種包含能夠提升高爾夫球的操控性與耐用性的熱塑性聚氨酯組合物的高爾夫球結構。The present invention relates to a golf ball structure, and more particularly to a golf ball structure comprising a thermoplastic polyurethane composition capable of improving the handling and durability of a golf ball.

隨著時代的進步,為了保持自身健康的水平,全世界皆掀起一股運動的熱潮。依據經濟部統計處的資料顯示,體育用品產值可高達新臺幣418億元。而在各式運動中,由於高爾夫球本身的運動強度較低,適於學習的人口層面廣,且高爾夫球可結合商務交流並作為一種社交活動,因此,高爾夫球的相關用品極具商機。With the advancement of the times, in order to maintain the level of their own health, the world has set off a wave of sports. According to the statistics of the Statistics Department of the Ministry of Economic Affairs, the output value of sports goods can reach as high as NT$41.8 billion. In all kinds of sports, because the golf ball itself has low exercise intensity, the population suitable for learning is wide, and the golf ball can be combined with business communication and as a social activity. Therefore, golf related articles are highly profitable.

目前市售之高爾夫球可具有單層或多層結構,而具有多層結構的高爾夫球可依照場地、所使用的球桿與打者的習慣等不同因素,提供不同組成的高爾夫球。因此,具有多層結構的高爾夫球相較於單層結構的高爾夫球具有較大的開發潛力。在具有多層結構的高爾夫球中,由於高爾夫球的表層直接與球桿接觸,因此高爾夫球的表層為影響其功能性的重要因素之一。Currently commercially available golf balls may have a single layer or a multi-layer structure, and golf balls having a multi-layer structure may provide golf balls of different compositions depending on factors such as the venue, the club used and the habit of the hitter. Therefore, a golf ball having a multi-layer structure has a large development potential compared to a golf ball having a single-layer structure. In a golf ball having a multi-layer structure, since the surface layer of the golf ball is directly in contact with the club, the surface layer of the golf ball is one of important factors affecting its functionality.

現今高爾夫球的表層主要為離子聚合型樹脂層,例如:杜邦 TM(DU PONT)公司所生產的沙林®樹脂 (Surlyn ®)。由於Surlyn ®具有良好的反彈性、耐用性與加工性,因此被廣泛地作為高爾夫球表層。然而Surlyn ®因為具有較大的硬度,其經過較大角度的球桿揮擊後,產生的後旋轉速有限,相應降低切球的功效。因此,當使用Surlyn ®作為表層結構的高爾夫球被擊上果嶺後,較容易出現滾動現象,亦即該高爾夫球產生不停球的現象,且該高爾夫球的表層結構容易受損,導致需要時常更換新的高爾夫球。因此,有必要開發一種能夠提升高爾夫球的操控性與耐用性的高爾夫球結構。 Today the major golf ball surface ionic polymeric resin layer, for example: DuPont TM (DU PONT) ® produced by the company sarin resin (Surlyn ®). Because Surlyn ® has a good bounce, durability and processability, it is widely used as golf ball cover. However, because the Surlyn ® has a larger hardness, after it passes through a large angle swing the club, the speed of rotation produced limited, a corresponding reduction in chipping effect. Therefore, when using Surlyn ® surface structure as a golf shot on the green, the more prone to rolling phenomenon, namely the phenomenon of the golf ball produces non-stop, and the surface structure of the golf ball is easily damaged, resulting in the need Change new golf balls from time to time. Therefore, it is necessary to develop a golf ball structure capable of improving the handling and durability of a golf ball.

鑒於上述問題,本創作之目的為提供一種高爾夫球結構,藉由提升高爾夫球的操控性與耐用性,以改善上述習知技術所產生的問題。In view of the above problems, the object of the present invention is to provide a golf ball structure which improves the problems caused by the above-mentioned conventional techniques by improving the handling and durability of the golf ball.

根據本創作之目的,提供一種高爾夫球結構,其包含球心內層以及包圍球心內層且包含熱塑性聚氨酯組合物的外層。所述熱塑性聚氨酯組合物包含由第一多異氰酸酯、第一多元醇組合物以及第一擴鏈劑組合物所組成的第一聚氨酯、由第二多異氰酸酯、第二多元醇組合物以及第二擴鏈劑組合物所組成的第二聚氨酯以及由第三多異氰酸酯、第三多元醇組合物以及第三擴鏈劑組合物所組成的第三聚氨酯,其中,第一多異氰酸酯、第一多元醇組合物與第一擴鏈劑組合物的莫耳數比為5:1:4, 其中,第二多異氰酸酯、第二多元醇組合物與第二擴鏈劑組合物的莫耳數比為4:1:3,其中,第三多異氰酸酯、第三多元醇組合物與第三擴鏈劑組合物的莫耳數比為3:1:2。For the purposes of this creation, a golf ball structure is provided that includes an inner core layer and an outer layer that surrounds the inner core layer and that includes the thermoplastic polyurethane composition. The thermoplastic polyurethane composition comprises a first polyurethane composed of a first polyisocyanate, a first polyol composition, and a first chain extender composition, a second polyisocyanate, a second polyol composition, and a a second polyurethane composed of a second chain extender composition and a third polyurethane composed of a third polyisocyanate, a third polyol composition and a third chain extender composition, wherein the first polyisocyanate, the first The molar ratio of the polyol composition to the first chain extender composition is 5:1:4, wherein the second polyisocyanate, the second polyol composition and the second chain extender composition are in the molar The number ratio is 4:1:3, wherein the third polyisocyanate, the third polyol composition and the third chain extender composition have a molar ratio of 3:1:2.

較佳地,第一聚氨酯、第二聚氨酯與第三聚氨酯的重量比為20~60份:10~50份:5~50份。更佳地,第一聚氨酯、第二聚氨酯與第三聚氨酯的重量比為35~45份:25~35份:15~20份。Preferably, the weight ratio of the first polyurethane, the second polyurethane to the third polyurethane is 20 to 60 parts: 10 to 50 parts: 5 to 50 parts. More preferably, the weight ratio of the first polyurethane, the second polyurethane to the third polyurethane is 35 to 45 parts: 25 to 35 parts: 15 to 20 parts.

較佳地,第一多異氰酸酯、第二多異氰酸酯以及第三多異氰酸酯各自獨立地選自甲苯二異氰酸酯、二苯甲烷二異氰酸酯、六亞甲基二異氰酸酯、異佛爾酮二異氰酸酯或其組合。Preferably, the first polyisocyanate, the second polyisocyanate, and the third polyisocyanate are each independently selected from the group consisting of toluene diisocyanate, diphenylmethane diisocyanate, hexamethylene diisocyanate, isophorone diisocyanate, or a combination thereof.

較佳地,第一多元醇組合物、第二多元醇組合物以及第三多元醇組合物各自獨立地選自聚酯、聚醚多元醇、聚酯多元醇或其組合。Preferably, the first polyol composition, the second polyol composition, and the third polyol composition are each independently selected from the group consisting of polyesters, polyether polyols, polyester polyols, or combinations thereof.

較佳地,第一多元醇組合物、第二多元醇組合物以及第三多元醇組合物各自獨立地選自聚丙烯酸丁酯、聚四氫呋喃或其組合。Preferably, the first polyol composition, the second polyol composition, and the third polyol composition are each independently selected from the group consisting of polybutyl acrylate, polytetrahydrofuran, or a combination thereof.

較佳地,第一擴鏈劑組合物、第二擴鏈劑組合物以及第三擴鏈劑組合物各自獨立地選自碳數C 1-C 5的醇類、碳數C 1-C 5胺類、碳數C 1-C 5烷類或其組合。 Preferably, the first chain extender composition, the second chain extender composition and the third chain extender composition are each independently selected from the group consisting of carbon C 1 -C 5 alcohols, carbon number C 1 -C 5 Amines, carbon number C 1 -C 5 alkanes or combinations thereof.

較佳地,第一擴鏈劑組合物、第二擴鏈劑組合物以及第三擴鏈劑組合物各自獨立地選自丁二醇、乙二胺、三羥甲基丙烷或其組合。Preferably, the first chain extender composition, the second chain extender composition, and the third chain extender composition are each independently selected from the group consisting of butanediol, ethylenediamine, trimethylolpropane, or a combination thereof.

較佳地,所述的熱塑性聚氨酯組合物更包含聚醚胺組合物。Preferably, the thermoplastic polyurethane composition further comprises a polyetheramine composition.

較佳地,第一聚氨酯、第二聚氨酯以及第三聚氨酯的總重量與聚醚胺組合物的重量的重量比為90~99份:1~10份。更佳地,第一聚氨酯、第二聚氨酯以及第三聚氨酯的總重量與聚醚胺組合物的重量的重量比為92~97份:3~8份。Preferably, the weight ratio of the total weight of the first polyurethane, the second polyurethane, and the third polyurethane to the weight of the polyetheramine composition is from 90 to 99 parts: from 1 to 10 parts. More preferably, the weight ratio of the total weight of the first polyurethane, the second polyurethane, and the third polyurethane to the weight of the polyetheramine composition is 92 to 97 parts: 3 to 8 parts.

本創作之高爾夫球結構具有下述優點:The golf structure of the present creation has the following advantages:

(1)本創作之高爾夫球結構可降低打擊時整個高爾夫球球體的壓縮現象,避免壓縮現象造成飛行距離減少,並同時提升打者擊球時的手感。(1) The golf structure of the present invention can reduce the compression phenomenon of the entire golf ball when hitting, avoiding the reduction of the flying distance caused by the compression phenomenon, and at the same time improving the feel of the hitter when hitting the ball.

(2) 本創作之高爾夫球結構可於短距離揮擊時產生更強力的後旋現象,使打者容易切球,以增加高爾夫球落地時的停球性,而減少高爾夫球於果嶺上滾動的情況。(2) The golf structure of this creation can produce a stronger back-spinning phenomenon when swiping in a short distance, making it easier for the hitter to cut the ball, to increase the ball stopping when the golf ball is landing, and to reduce the rolling of the golf ball on the green. Case.

(3)本創作之高爾夫球結構相較於市售高爾夫球,其具有更佳的耐打性,可承受速度160 f/s 的擊球至少500次以上,且亦具有更佳的耐切性,使用60球桿以速度40 m/s打擊100次後,未發現高爾夫球結構之表面受損的情況。(3) The golf ball structure of the present invention has better resistance to hitting than a commercially available golf ball, can withstand a hitting speed of 160 f/s at least 500 times, and has better cut resistance. After hitting 100 times with a 60-bar at a speed of 40 m/s, no damage was observed to the surface of the golf ball structure.

(4)在本創作之高爾夫球結構的外層中,包含具有可形成結晶的硬鏈段與可吸收應力的軟鏈段的熱塑性聚氨酯組合物,因此能夠依照不同的使用需求,客製化調整高爾夫球結構,以增加本創作之應用廣泛性。(4) In the outer layer of the golf ball structure of the present invention, a thermoplastic polyurethane composition having a hard segment capable of forming crystals and a soft segment capable of absorbing stress is provided, so that golf can be customized according to different use requirements. The ball structure to increase the application of this creation.

(5)有別於傳統聚氨酯(PU)容易結晶而導致其性質較脆的情況,本創作混摻多種添加物以破壞結晶,因此可加強本創作之高爾夫球結構的韌性。(5) Unlike the case where the conventional polyurethane (PU) is easily crystallized and its properties are brittle, the present invention blends various additives to destroy the crystal, thereby enhancing the toughness of the golf structure of the present invention.

為使上述目的、技術特徵及實際實施後之效益更易於使本領域具通常知識者理解,將於下文中以實施例搭配圖式更詳細地說明。此外,於附圖中組成構件的尺寸和厚度為更易於理解與便於描述,而任意的表示,但本創作不以此所侷限。In order to make the above objects, technical features, and actual implementation benefits more readily understood by those of ordinary skill in the art, the embodiments will be described in more detail below with reference to the drawings. Moreover, the size and thickness of the constituent members in the drawings are more easily understood and described, and are arbitrarily indicated, but the present invention is not limited thereto.

參照第1圖,其係為本創作之高爾夫球結構之熱塑性聚氨酯組合物的製備流程圖。Referring to Figure 1, it is a flow chart for the preparation of a thermoplastic polyurethane composition of the present golf ball structure.

步驟S11、S12與S13中,分別先將多異氰酸酯與多元醇組合物混合,並加熱反應以獲得預聚物。其中,以莫耳數5:1的比例混合第一多異氰酸酯與第一多元醇組合物後,使其反應並獲得第一預聚物;以莫耳數4:1的比例混合第二多異氰酸酯與第二多元醇組合物後,使其反應並獲得第二預聚物;以莫耳數3:1的比例混合第三多異氰酸酯與第三多元醇組合物後,使其反應並獲得第三預聚物。其中,第一多異氰酸酯、第二多異氰酸酯與第三多異氰酸酯可為相同或不同;第一多元醇組合物、第二多元醇組合物與第三多元醇組合物可為相同或不同。In steps S11, S12 and S13, the polyisocyanate is first mixed with the polyol composition, and the reaction is heated to obtain a prepolymer. Wherein the first polyisocyanate and the first polyol composition are mixed in a molar ratio of 5:1, and then reacted to obtain a first prepolymer; the second most mixed in a molar ratio of 4:1. After the isocyanate and the second polyol composition, the reaction is carried out to obtain a second prepolymer; the third polyisocyanate and the third polyol composition are mixed in a molar ratio of 3:1, and then reacted and A third prepolymer is obtained. Wherein, the first polyisocyanate, the second polyisocyanate and the third polyisocyanate may be the same or different; the first polyol composition, the second polyol composition and the third polyol composition may be the same or different .

步驟S21、S22與S23中,分別將獲得的預聚物與擴鏈劑組合物混合,並進行擴鏈反應以獲得聚氨酯。其中,以莫耳數6:4的比例混合第一預聚物與第一擴鏈劑組合物,使其反應並獲得第一聚氨酯;以莫耳數5:3的比例混合第二預聚物與第二擴鏈劑組合物,使其反應並獲得第二聚氨酯;以莫耳數4:2的比例混合第三預聚物與第三擴鏈劑組合物,使其反應並獲得第三聚氨酯。其中,第一擴鏈劑組合物、第二擴鏈劑組合物與第三擴鏈劑組合物可為相同或不同。In steps S21, S22 and S23, the obtained prepolymer and the chain extender composition are respectively mixed and subjected to a chain extension reaction to obtain a polyurethane. Wherein, the first prepolymer and the first chain extender composition are mixed in a molar ratio of 6:4, reacted to obtain a first polyurethane; and the second prepolymer is mixed at a molar ratio of 5:3. And reacting with the second chain extender composition to obtain a second polyurethane; mixing the third prepolymer and the third chain extender composition in a molar ratio of 4:2, reacting it and obtaining a third polyurethane . Wherein, the first chain extender composition, the second chain extender composition and the third chain extender composition may be the same or different.

步驟S31、S32與S33中,分別將獲得的聚氨酯進行塑膠造粒,以獲得聚氨酯塑膠粒(plastic pellets)。In steps S31, S32 and S33, the obtained polyurethanes are respectively plastic granulated to obtain plastic pellets.

步驟S40中,將獲得的聚氨酯塑膠粒以不同重量比進行物理混摻,並獲得本創作之熱塑性聚氨酯組合物。In step S40, the obtained polyurethane plastic granules are physically blended in different weight ratios, and the thermoplastic polyurethane composition of the present invention is obtained.

此外,上述第一聚氨酯、第二聚氨酯與第三聚氨酯的重量比,較佳地為20~60份:10~50份:5~50份,更佳地為35~45份:25~35份:15~20份。藉由調整第一聚氨酯、第二聚氨酯與第三聚氨酯的比例,可控制聚氨酯組合物的性質。由於多異氰酸酯與擴鏈劑組合物屬於硬鏈段,硬鏈段因分子間作用力而形成結晶區,性質較為脆硬,而多元醇組合物則屬於軟鍵段,其可吸收應力以維持高分子的形狀,性質較為柔韌。因此,當聚氨酯組合物需要具有較高硬度時,可混合較多的硬鏈段使硬度提高。故本創作之高爾夫球結構包含的熱塑性聚氨酯組合物,可依照不同需求調整混合比例,使本創作能夠作為一種具有廣泛應用性的高爾夫球結構。Further, the weight ratio of the first polyurethane, the second polyurethane to the third polyurethane is preferably 20 to 60 parts: 10 to 50 parts: 5 to 50 parts, more preferably 35 to 45 parts: 25 to 35 parts. : 15~20 servings. The properties of the polyurethane composition can be controlled by adjusting the ratio of the first polyurethane, the second polyurethane to the third polyurethane. Since the polyisocyanate and chain extender composition are hard segments, the hard segment forms a crystalline region due to intermolecular forces, and the properties are brittle and hard, while the polyol composition belongs to a soft bond segment, which absorbs stress to maintain high The shape of the molecule is more flexible. Therefore, when the polyurethane composition is required to have a high hardness, more hard segments can be mixed to increase the hardness. Therefore, the thermoplastic polyurethane composition contained in the golf structure of the present invention can adjust the mixing ratio according to different needs, so that the creation can be used as a golf ball structure with wide application.

接續上述,本創作之高爾夫球結構的一實施例的組成如表1所示。Following the above, the composition of an embodiment of the golf ball structure of the present invention is shown in Table 1.

表1 <TABLE border="1" borderColor="#000000" width="85%"><TBODY><tr><td> </td><td> 聚氨酯A </td><td> 聚氨酯B </td><td> 聚氨酯C </td><td> 聚氨酯D </td><td> 聚氨酯E </td></tr><tr><td> MDI </td><td> 5 </td><td> 5 </td><td> 5 </td><td> 4 </td><td> 3 </td></tr><tr><td> PBA2000 </td><td> 1 </td><td> 0 </td><td> 0.5 </td><td> 1 </td><td> 1 </td></tr><tr><td> PTMEG2000 </td><td> 0 </td><td> 1 </td><td> 0.5 </td><td> 0 </td><td> 0 </td></tr><tr><td> EDA </td><td> 0.2 </td><td> 0.2 </td><td> 0.2 </td><td> 0.1 </td><td> 0.1 </td></tr><tr><td> 1,4BD </td><td> 3.4 </td><td> 3.4 </td><td> 3.4 </td><td> 2.6 </td><td> 1.7 </td></tr><tr><td> TMP </td><td> 0.4 </td><td> 0.4 </td><td> 0.4 </td><td> 0.3 </td><td> 0.2 </td></tr></TBODY></TABLE>Table 1  <TABLE border="1" borderColor="#000000" width="85%"><TBODY><tr><td> </td><td> Polyurethane A </td><td> Polyurethane B </td ><td> Polyurethane C </td><td> Polyurethane D </td><td> Polyurethane E </td></tr><tr><td> MDI </td><td> 5 </td ><td> 5 </td><td> 5 </td><td> 4 </td><td> 3 </td></tr><tr><td> PBA2000 </td><td > 1 </td><td> 0 </td><td> 0.5 </td><td> 1 </td><td> 1 </td></tr><tr><td> PTMEG2000 < /td><td> 0 </td><td> 1 </td><td> 0.5 </td><td> 0 </td><td> 0 </td></tr><tr> <td> EDA </td><td> 0.2 </td><td> 0.2 </td><td> 0.2 </td><td> 0.1 </td><td> 0.1 </td></ Tr><tr><td> 1,4BD </td><td> 3.4 </td><td> 3.4 </td><td> 3.4 </td><td> 2.6 </td><td> 1.7 </td></tr><tr><td> TMP </td><td> 0.4 </td><td> 0.4 </td><td> 0.4 </td><td> 0.3 </ Td><td> 0.2 </td></tr></TBODY></TABLE>

其中,第一聚氨酯可選自聚氨酯A、聚氨酯B與聚氨酯C中的任一種,第二聚氨酯可為聚氨酯D,且第三聚氨酯可為聚氨酯E。第一多異氰酸酯、第二多異氰酸酯與第三多異氰酸酯皆選用二苯基甲烷二異氰酸酯 (MDI,CAS NO.101-68-8)。第一多元醇組合物、第二多元醇組合物與第三多元醇組合物各自獨立地選用聚丙烯酸丁酯(PBA2000,Butyl acrylate resin,分子量2000)、聚四氫呋喃 (PBA2000,Polytetrahydrofuran,分子量2000)或其組合。第一擴鏈劑組合物、第二擴鏈劑組合物與第三擴鏈劑組合物各自獨立地選用乙二胺 (EDA,Ethylenediamine,CAS NO.107-15-3)、丁二醇 (1,4BD,Butanediol,CAS NO.110-63-5)、1,1,1-三羥甲基丙烷 (TMP,1,1,1-Trimethylolpropane,CAS NO.77-99-6) 或其組合。Wherein, the first polyurethane may be selected from any one of polyurethane A, polyurethane B and polyurethane C, the second polyurethane may be polyurethane D, and the third polyurethane may be polyurethane E. The first polyisocyanate, the second polyisocyanate and the third polyisocyanate are selected from diphenylmethane diisocyanate (MDI, CAS No. 101-68-8). The first polyol composition, the second polyol composition and the third polyol composition are each independently selected from polybutyl acrylate (PBA2000, Butyl acrylate resin, molecular weight 2000), polytetrahydrofuran (PBA2000, Polytetrahydrofuran, molecular weight). 2000) or a combination thereof. The first chain extender composition, the second chain extender composition and the third chain extender composition are each independently selected from ethylenediamine (EDA, Ethylenediamine, CAS NO. 107-15-3), butanediol (1). , 4BD, Butanediol, CAS NO. 110-63-5), 1,1,1-trimethylolpropane (TMP, 1,1,1-Trimethylolpropane, CAS NO. 77-99-6) or a combination thereof.

而本實施例的實驗流程如下所述: (1)依照表1的比例,分別將MDI、PBA2000 與PBA2000於70℃的溫度下均勻混合,使其反應1小時,並分別獲得預聚物。 (2)依照表1的比例,分別將EDA、1,4BD與TMP混合備用。 (3) 依照表1的比例,分別地將混合後的EDA、1,4BD與TMP與獲得的預聚物混合並攪拌1分鐘。 (4)接續前步驟,分別地將混合物倒入110℃的模具中,置於110℃的烘箱持續6個小時,使其硬化(curing)以使混合物能夠完全反應。 (5)分別將硬化後的聚氨酯進行造粒,以分別獲得聚氨酯A、B、C、D與E的塑膠粒。其中,造粒的步驟可為所屬領域中具有通常知識者通用或常用的任何能夠造粒的方法。 (6)將聚氨酯A、B、C、D與E的塑膠粒以不同重量比進行物理混摻,亦即僅進行物理混合而非進行化學反應,並獲得本創作之高爾夫球結構包含的熱塑性聚氨酯組合物。The experimental procedure of this example is as follows: (1) According to the ratio of Table 1, MDI, PBA2000 and PBA2000 were uniformly mixed at a temperature of 70 ° C, respectively, and allowed to react for 1 hour, and prepolymers were respectively obtained. (2) According to the ratio of Table 1, EDA, 1, 4BD and TMP are mixed and used separately. (3) According to the ratio of Table 1, the mixed EDA, 1,4BD and TMP were separately mixed with the obtained prepolymer and stirred for 1 minute. (4) Prior to the subsequent steps, the mixture was separately poured into a mold at 110 ° C, placed in an oven at 110 ° C for 6 hours, and cured to allow the mixture to completely react. (5) The hardened polyurethanes were respectively granulated to obtain plastic granules of polyurethanes A, B, C, D and E, respectively. Among them, the step of granulating may be any method capable of granulation which is common or commonly used by those skilled in the art. (6) The plastic granules of polyurethanes A, B, C, D and E are physically mixed in different weight ratios, that is, only physical mixing is performed instead of chemical reaction, and the thermoplastic polyurethane contained in the golf structure of the present invention is obtained. combination.

接續上述,在本創作之較佳實施例中,聚氨酯A、B、C、D與E的塑膠粒的混合比例如表2所示,並獲得配方1、2與3的熱塑性聚氨酯組合物。Following the above, in the preferred embodiment of the present invention, the mixing ratio of the plastic granules of the polyurethanes A, B, C, D and E is as shown in Table 2, and the thermoplastic polyurethane compositions of the formulations 1, 2 and 3 are obtained.

表2 <TABLE border="1" borderColor="#000000" width="85%"><TBODY><tr><td> </td><td> A </td><td> B </td><td> C </td><td> D </td><td> E </td></tr><tr><td> 配方1 </td><td> 40份 </td><td> - </td><td> - </td><td> 30份 </td><td> 20份 </td></tr><tr><td> 配方2 </td><td> - </td><td> 40份 </td><td> - </td><td> 30份 </td><td> 20份 </td></tr><tr><td> 配方3 </td><td> - </td><td> - </td><td> 40份 </td><td> 30份 </td><td> 20份 </td></tr></TBODY></TABLE>此處,「-」符號代表未添加。 Table 2  <TABLE border="1" borderColor="#000000" width="85%"><TBODY><tr><td> </td><td> A </td><td> B </td>< Td> C </td><td> D </td><td> E </td></tr><tr><td> Recipe 1 </td><td> 40 </td><td > - </td><td> - </td><td> 30 copies</td><td> 20 copies</td></tr><tr><td> Recipe 2 </td><td > - </td><td> 40 copies</td><td> - </td><td> 30 copies</td><td> 20 copies</td></tr><tr><td > Recipe 3 </td><td> - </td><td> - </td><td> 40 copies</td><td> 30 copies</td><td> 20 copies</td> </tr></TBODY></TABLE> Here, the "-" symbol means not added.  

如表2所示,目前市售之高爾夫球表層材料,其配方如聚氨酯A或聚氨酯B所示,並未添加聚氨酯C、D、E或其組合。然而,本創作之高爾夫球結構包含之熱塑性聚氨酯組合物,因為添加聚氨酯C、D、E或其組合,使熱塑性聚氨酯組合物的硬度增強,其測試結果如表3所示。As shown in Table 2, currently commercially available golf club skin materials, such as polyurethane A or polyurethane B, are not added with polyurethane C, D, E or a combination thereof. However, the golf ball structure of the present invention comprises a thermoplastic polyurethane composition, and the hardness of the thermoplastic polyurethane composition is enhanced by the addition of the polyurethanes C, D, E or a combination thereof, and the test results are shown in Table 3.

表3 <TABLE border="1" borderColor="#000000" width="85%"><TBODY><tr><td> </td><td> 160f/s耐打 </td><td> 40m/s耐切60度球桿(有裂痕) </td></tr><tr><td> 配方1 </td><td> 500下 以上未破 </td><td> 100下 以上 </td></tr><tr><td> 配方2 </td><td> 250下 </td><td> 35下 </td></tr><tr><td> 配方3 </td><td> 300下 </td><td> 40下 </td></tr></TBODY></TABLE>table 3  <TABLE border="1" borderColor="#000000" width="85%"><TBODY><tr><td> </td><td> 160f/s resistant to fight</td><td> 40m/ s cut-resistant 60-degree club (with cracks) </td></tr><tr><td> Recipe 1 </td><td> 500 or more unbroken</td><td> 100 or more</ Td></tr><tr><td> Recipe 2 </td><td> 250下</td><td> 35下</td></tr><tr><td> Recipe 3 </ Td><td> 300下</td><td> 40下</td></tr></TBODY></TABLE>

表3為根據表2的配方進行耐打與耐切性測試的結果。耐打測試係利用美國ADC炮擊測試機進行測試。而耐切測試係使用台灣自製高爾夫球打擊機,於桿面60度時進行測試。其中,由耐打測試可知,相較於僅能承受250下與300下的配方2與配方3,配方1可承受500下以上仍未破裂,因此配方1具有較佳之耐打性。而由耐切性測試中可知,相較於僅能承受35下與40下的配方2與配方3,配方1維持100下以上時才出現裂痕,因此配方1具有較佳之耐切性。Table 3 shows the results of the resistance test and the cut resistance test according to the formulation of Table 2. The resistance test was conducted using the US ADC bombardment tester. The cut-resistant test was carried out using a Taiwan-made golf hitting machine at 60 degrees on the face. Among them, it can be seen from the resistance test that the formulation 1 can withstand more than 500 times without breaking, as compared with the formulation 2 and the formulation 3 which can only withstand 250 and 300, and therefore the formulation 1 has better resistance to abrasion. From the endurance test, it can be seen that the formulation 1 has better cut resistance than the formulation 2 and the formulation 3 which can only withstand 35 and 40, and the formulation 1 is maintained at 100 or more.

接續上述較佳實施例,在本創作之一更佳實施例中,將配方1的熱塑性聚氨酯混合物與聚醚胺組合物進行物理混摻,其混摻的重量比如表4所示。Following the preferred embodiment described above, in a preferred embodiment of the present invention, the thermoplastic polyurethane blend of Formulation 1 was physically blended with the polyetheramine composition, and the weight of the blend was as shown in Table 4.

表4 <TABLE border="1" borderColor="#000000" width="85%"><TBODY><tr><td> </td><td> 配方1 </td><td> Jeffamine<sup>®</sup> D-4000 </td><td> Jeffamine<sup>®</sup> T-4000 </td><td> MDI </td></tr><tr><td> 完成品1 </td><td> 95份 </td><td> - </td><td> - </td><td> - </td></tr><tr><td> 完成品2 </td><td> 95份 </td><td> 2份 </td><td> 2份 </td><td> 1份 </td></tr></TBODY></TABLE>此處,「-」符號代表未添加。 Table 4  <TABLE border="1" borderColor="#000000" width="85%"><TBODY><tr><td> </td><td> Recipe 1 </td><td> Jeffamine<sup>® </sup> D-4000 </td><td> Jeffamine<sup>®</sup> T-4000 </td><td> MDI </td></tr><tr><td> Finished product 1 </td><td> 95 copies</td><td> - </td><td> - </td><td> - </td></tr><tr><td> Finished product 2 </td><td> 95 copies</td><td> 2 copies</td><td> 2 copies</td><td> 1 copy</td></tr></TBODY>< /TABLE>Here, the "-" symbol means not added.  

如表4所示,其中,聚醚胺組合物可選自聚醚胺類、多異氰酸酯、或其組合。聚醚胺組合物較佳地為聚醚胺(Jeffamine ®D-4000,polyetheramine,分子量4000)、聚醚胺(Jeffamine ®T-4000,polyetheramine,分子量4000)、MDI或其組合。此外,進行完成品1與完成品2之性質測試,其測試結果如表5所示。 As shown in Table 4, wherein the polyetheramine composition may be selected from the group consisting of polyetheramines, polyisocyanates, or combinations thereof. The composition is preferably a polyether amine is a polyether amine (Jeffamine ® D-4000, polyetheramine , molecular weight 4000), the polyether amine (Jeffamine ® T-4000, polyetheramine , molecular weight 4000), the MDI or combinations thereof. In addition, the properties of the finished product 1 and the finished product 2 were tested, and the test results are shown in Table 5.

表5 <TABLE border="1" borderColor="#000000" width="85%"><TBODY><tr><td> </td><td> 160f/s反彈係數COR </td><td> 40m/s耐切60度球桿(有裂痕) </td></tr><tr><td> 完成品1 </td><td> 0.740 </td><td> 70下 </td></tr><tr><td> 完成品2 </td><td> 0.755 </td><td> 100下 以上 </td></tr></TBODY></TABLE>table 5  <TABLE border="1" borderColor="#000000" width="85%"><TBODY><tr><td> </td><td> 160f/s rebound coefficient COR </td><td> 40m /s cut-resistant 60-degree club (with cracks) </td></tr><tr><td> Finished product 1 </td><td> 0.740 </td><td> 70下</td>< /tr><tr><td> Finished Product 2 </td><td> 0.755 </td><td> More than 100</td></tr></TBODY></TABLE>

表5為根據表4的配方進行反彈係數COR測試與耐切性測試的結果。反彈係數COR測試係利用美國ADC炮擊測試機進行測試。而耐切測試係使用台灣自製高爾夫球打擊機,於桿面60度時進行測試。如表5所示,其中,相較於未添加聚醚胺組合物的完成品1,完成品2可使含有其之高爾夫球的反彈係數及耐切性有明顯之提升。Table 5 shows the results of the rebound coefficient COR test and the cut resistance test according to the formulation of Table 4. The rebound coefficient COR test was tested using the US ADC bombardment tester. The cut-resistant test was carried out using a Taiwan-made golf hitting machine at 60 degrees on the face. As shown in Table 5, the finished product 2 can significantly improve the rebound coefficient and the cut resistance of the golf ball containing the same as the finished product 1 to which the polyetheramine composition is not added.

於實務上,將配方1的熱塑性聚氨酯混合物與聚醚胺組合物進行物理混摻後,所獲得的完成品2的塑膠粒即可作為商業販售產品。消費者購買所述塑膠粒後,可藉由各種塑膠粒的加工方式進行使用,例如:使用射出成型機將所述塑膠粒進行射出成型。其中,因為各種塑膠粒的加工方式皆包含加熱,因此於加工製程中,所述塑膠粒會因為溫度上升,在射出成型機內快速反應,並產生交聯 (cross-link)的情況。當溫度上升後,所含有的MDI會與聚醚胺的胺基 (-NH 2)反應,形成聚脲 (polyurea),使所述塑膠粒形成性質更為強韌的聚氨酯-聚脲 (polyurethane-polyurea)的形式。 In practice, after the thermoplastic polyurethane mixture of Formulation 1 and the polyetheramine composition are physically blended, the obtained plastic pellet of Finished Product 2 can be used as a commercial product. After the consumer purchases the plastic granules, the plastic granules can be processed by various processing methods, for example, the plastic granules are injection molded using an injection molding machine. Among them, since the processing methods of various plastic granules include heating, in the processing process, the plastic granules rapidly react in the injection molding machine due to temperature rise, and cross-linking occurs. When the temperature rises, the MDI contained will react with the amine group (-NH 2 ) of the polyetheramine to form polyurea, which makes the plastic particles form a more rigid polyurethane-polyurea. The form of polyurea).

接續上述實施例,使用射出成型機將完成品2製成高爾夫球,並與市售高爾夫球進行分析比較。Following the above embodiment, the finished product 2 was made into a golf ball using an injection molding machine, and analyzed and compared with a commercially available golf ball.

參照第2圖,其係本創作之高爾夫球結構之實施例一的結構示意圖。Referring to Fig. 2, it is a schematic structural view of the first embodiment of the golf ball structure of the present invention.

如第2圖所示,球心內層100可選用BR人造膠及添加物,控制溫度於約160~170℃,進行熱壓成型,並將尺寸研磨至直徑35~42 mm。且外層300係選用完成品2的塑膠粒,控制溫度於約180~220 ℃,進行表層射出成型,其射出厚度為0.5~1.5 mm。此外,實施例一可做為高爾夫練習球或比賽球。由於實施例一製程簡單,其製造成本較低,因此較佳地,實施例一可做為高爾夫練習球。As shown in Fig. 2, the inner core layer 100 can be made of BR artificial glue and additives, and the temperature is controlled at about 160-170 ° C for hot press forming, and the size is ground to a diameter of 35 to 42 mm. And the outer layer 300 is selected from the plastic pellet of the finished product 2, and the temperature is controlled at about 180-220 ° C, and the surface layer is injection-molded, and the thickness of the injection is 0.5 to 1.5 mm. In addition, the first embodiment can be used as a golf practice ball or a game ball. Since the manufacturing process of the first embodiment is simple and the manufacturing cost is low, the first embodiment can be used as a golf practice ball.

參照第3圖,其係本創作之高爾夫球結構之實施例二的結構示意圖。Referring to Fig. 3, it is a schematic structural view of a second embodiment of the golf ball structure of the present invention.

如第3圖所示,球心內層100可選用BR人造膠及添加物,控制溫度於約160~170℃,進行熱壓成型,並將尺寸研磨至直徑35~42 mm。中間層200係選用離子型樹脂 (IONOMER RESIN),控制溫度於約170~180 ℃,進行第二層射出成型,其射出厚度為0.5~2 mm。外層300係選用完成品2的塑膠粒,控制溫度於約180~220 ℃,進行表層射出成型,其射出厚度為0.1~1.5 mm。此外,實施例二可做為高爾夫練習球或比賽球。由於實施例二製程較為複雜,但其具備有緩衝效果的中間層,因此較佳地,實施例二可做為高爾夫比賽球。As shown in Fig. 3, the inner core layer 100 can be made of BR artificial glue and additives, and the temperature is controlled at about 160-170 ° C for hot press forming, and the size is ground to a diameter of 35 to 42 mm. The intermediate layer 200 is made of an ionic resin (IONOMER RESIN), and the second layer is injection-molded at a controlled temperature of about 170 to 180 ° C, and has a thickness of 0.5 to 2 mm. The outer layer 300 is made of plastic pellets of finished product 2, and the temperature is controlled at about 180-220 ° C for surface injection molding, and the thickness of the injection is 0.1 to 1.5 mm. In addition, the second embodiment can be used as a golf practice ball or a game ball. Since the process of the second embodiment is relatively complicated, but it has an intermediate layer with a buffering effect, it is preferable that the second embodiment can be used as a golf game ball.

將經過上述製程所得的本創作之實施例一與實施例二的高爾夫球結構置於室溫24℃環境,放置一周後進行比較測試,測試方式如下所述: (1)壓縮:美國ADC壓縮測試機 (2)反彈係數COR:美國ADC炮擊測試機 (3)表面硬度:日本JIS-D (4)耐切:台灣自製高爾夫球打擊機,桿面60度 (5)耐打:美國ADC炮擊測試機The golf ball structure of the first embodiment and the second embodiment of the present invention obtained in the above process are placed in a room temperature of 24 ° C and placed in a comparison test for one week. The test method is as follows: (1) Compression: US ADC compression test Machine (2) rebound coefficient COR: US ADC bombardment test machine (3) Surface hardness: Japan JIS-D (4) Cut resistance: Taiwan homemade golf hitting machine, face 60 degrees (5) resistance: US ADC bombardment test machine

根據上述測試,選出實施例一與實施例二的較佳數值,分別稱為實施例三與實施例四,並與市售之高爾夫球產品進行比較。Based on the above tests, the preferred values of Example 1 and Example 2 were selected and referred to as Example 3 and Example 4, respectively, and compared with commercially available golf products.

實施例三之球心內層100的直徑為39.8 mm且外層300厚度為1.5 mm,因此可得球體的直徑為42.8 mm的成品。其與市售之高爾夫球產品分別進行上述測試,測試結果如表6所示。The core inner layer 100 of the third embodiment has a diameter of 39.8 mm and the outer layer 300 has a thickness of 1.5 mm, so that a finished product having a sphere diameter of 42.8 mm can be obtained. The above tests were carried out separately from the commercially available golf products, and the test results are shown in Table 6.

表6 <TABLE border="1" borderColor="#000000" width="85%"><TBODY><tr><td> </td><td> 壓縮 </td><td> 160f/s 反彈係數(COR) </td><td> 表面硬度 </td><td> 40m/s 耐切60度 </td><td> 160f/s 耐打 </td></tr><tr><td> Surlyn<sup>®</sup> 練習球 </td><td> 95 </td><td> 0.740 </td><td> 67 </td><td> 40下 </td><td> 200下 </td></tr><tr><td> Bridgestone TPU練習球 </td><td> 90 </td><td> 0.720 </td><td> 67 </td><td> 100下 </td><td> 500下 </td></tr><tr><td> 實施例三 (VPLUS 練習球) </td><td> 80 </td><td> 0.730 </td><td> 56 </td><td> 100下 </td><td> 500下 </td></tr></TBODY></TABLE>Table 6  <TABLE border="1" borderColor="#000000" width="85%"><TBODY><tr><td> </td><td> Compression</td><td> 160f/s rebound coefficient ( COR) </td><td> Surface Hardness </td><td> 40m/s Cutoff 60°</td><td> 160f/s 耐打</td></tr><tr><td> Surlyn<sup>®</sup> practice ball</td><td> 95 </td><td> 0.740 </td><td> 67 </td><td> 40下</td><td > 200下</td></tr><tr><td> Bridgestone TPU exercise ball</td><td> 90 </td><td> 0.720 </td><td> 67 </td>< Td> 100下</td><td> 500下</td></tr><tr><td> Example 3 (VPLUS practice ball) </td><td> 80 </td><td> 0.730 </td><td> 56 </td><td> 100 </td><td> 500 </td></tr></TBODY></TABLE>

如表6所示,將實施例三,亦即自有品牌VPLUS的練習球,與原設計Surlyn ®外皮練習球進行上述測試。可得知,使用熱塑性聚氨酯組合物作為外層的實施例三,其之各種手感與耐打性皆有明顯提升。此外,將其與市面上同等級練習球,例如:知名高爾夫品牌Bridgestone的練習球,進行比較。可知,實施例三的壓縮程度及表面硬度較低,因此可改善傳統練習球打擊手感過硬的問題,且亦不因為壓縮程度低,而導致反彈係數下降,仍保持高反彈係數以維持飛行距離。同時,實施例三使用60球桿以40 m/s速度進行耐打測試,於擊球100次後並無發現表面受損,可知其可達到柔軟又耐切的效果。此外,實施例三經過ADC炮擊測試以160 f/s速度連續打擊下,可承受至少500次以上撞擊,代表其具有良好的耐用性。因此可知,實施例三之搭配方式不論是手感、耐打性不僅優於傳統Surlyn ®外層練習球,且手感、距離皆優於市面上同等級知名品牌。 As shown in Table 6, the third embodiment, i.e., its own brand VPLUS practice balls, to perform such tests with the original design Surlyn ® sheath practice balls. It can be seen that in the third embodiment using the thermoplastic polyurethane composition as the outer layer, various hand feelings and resistance to abrasion are significantly improved. In addition, compare it to the same level of practice balls on the market, such as the ball of the famous golf brand Bridgestone. It can be seen that the compression degree and the surface hardness of the third embodiment are low, so that the problem of the traditional practice ball hitting hard feeling can be improved, and the rebound coefficient is not lowered due to the low degree of compression, and the high rebound coefficient is maintained to maintain the flight distance. At the same time, in the third embodiment, the 60-ball was used for the resistance test at a speed of 40 m/s, and no surface damage was observed after hitting the ball 100 times, and it was found that it could achieve a soft and cut-resistant effect. In addition, the third embodiment can withstand at least 500 impacts after being continuously struck by the ADC bombardment test at a speed of 160 f/s, indicating that it has good durability. Thus it is seen, according to a third embodiment with a way of either feel resistance, resistance to fight not only the outer layer of Surlyn ® is superior to the traditional practice balls, and feel, better than the market are from the same class of well-known brands.

實施例四之球心內層100的直徑為38.5 mm、中間層200的厚度為1. 35 mm且外層300厚度為0.8 mm,因此可得球體的直徑為42.8 mm成品。其與市售之高爾夫球產品分別進行上述測試,測試結果如表7所示。The core inner layer 100 of the fourth embodiment has a diameter of 38.5 mm, the intermediate layer 200 has a thickness of 1.35 mm, and the outer layer 300 has a thickness of 0.8 mm, so that the spherical body has a diameter of 42.8 mm. The above tests were carried out separately from the commercially available golf products, and the test results are shown in Table 7.

表7 <TABLE border="1" borderColor="#000000" width="85%"><TBODY><tr><td> </td><td> 壓縮 </td><td> 160f/s 反彈係數(COR) </td><td> 表面硬度 </td><td> 40m/s 耐切60度 </td></tr><tr><td> Surlyn<sup>®</sup> 練習球 </td><td> 95 </td><td> 0.741 </td><td> 63 </td><td> 40下 </td></tr><tr><td> PRO V1 </td><td> 95 </td><td> 0.743 </td><td> 62 </td><td> 100下 </td></tr><tr><td> PRO V1X </td><td> 100 </td><td> 0.748 </td><td> 62 </td><td> 100下 </td></tr><tr><td> 實施例四 VPLUS 比賽球 </td><td> 90 </td><td> 0.755 </td><td> 56 </td><td> 100下 </td></tr></TBODY></TABLE>Table 7  <TABLE border="1" borderColor="#000000" width="85%"><TBODY><tr><td> </td><td> Compression</td><td> 160f/s rebound coefficient ( COR) </td><td> Surface Hardness </td><td> 40m/s Cutoff 60°</td></tr><tr><td> Surlyn<sup>®</sup> Exercise Ball< /td><td> 95 </td><td> 0.741 </td><td> 63 </td><td> 40下</td></tr><tr><td> PRO V1 </ Td><td> 95 </td><td> 0.743 </td><td> 62 </td><td> 100 </td></tr><tr><td> PRO V1X </td ><td> 100 </td><td> 0.748 </td><td> 62 </td><td> 100下</td></tr><tr><td> Example 4 VPLUS game ball </td><td> 90 </td><td> 0.755 </td><td> 56 </td><td> 100 </td></tr></TBODY></TABLE>

如表7所示,將實施例四,亦即自有品牌VPLUS的比賽球與原設計Surlyn ®外皮比賽球比較後可得知,使用熱塑性聚氨酯組合物作為外層的實施例四,其之手感與表面耐切性皆有明顯提升。此外,與知名高爾夫品牌Titleist PRO V1、PRO V1x的兩種比賽球進行比較。可知,實施例四可降低整顆球的壓縮,使得打者擊球時的手感提升,亦不會因為壓縮較多而減少飛行距離 (COR)。同時,實施例四相較於知名品牌更為柔軟,其可於短距離揮擊時產生更強力後旋,以增加落地時停球性,減少滾動。此外,實施例四球使用60球桿以40 m/s速度進行耐打測試,於擊球100次後並無發現表面受損,可知其可達到柔軟又耐切的效果。因此可知,實施例四之此搭配方式不論是手感、耐切性皆優於傳統Surlyn ®外層比賽球,且在手感、距離、耐切性,皆優於市面上同等級知名品牌。 As shown in Table 7, the fourth embodiment, i.e., the own brand VPLUS original game ball game ball sheath Surlyn ® comparison with the known design, a thermoplastic polyurethane composition as the outer layer of the fourth embodiment, which is the feel and The surface cut resistance is obviously improved. In addition, it is compared with the two game balls of the famous golf brands Titleist PRO V1 and PRO V1x. It can be seen that the fourth embodiment can reduce the compression of the whole ball, so that the feel of the hitter when hitting the ball is improved, and the flight distance (COR) is not reduced because of the more compression. At the same time, the fourth embodiment is softer than the well-known brands, which can produce a stronger back spin when swiping in a short distance, so as to increase the ball stopping when landing, and reduce rolling. In addition, the fourth ball of the example was subjected to a resistance test at a speed of 40 m/s using a 60-ball, and no surface damage was observed after hitting the ball 100 times, and it was found that it was soft and cut-resistant. Thus understood, according to a fourth embodiment of this embodiment with both feel, cut resistance properties are superior to the conventional Surlyn ® outer ball game, and the touch distance, cut resistance properties, are better than the same level of well-known brands on the market.

參照第4圖與第5圖,其分別為本創作之高爾夫球結構之實施例五與實施例六的結構示意圖。Referring to Figures 4 and 5, which are respectively a schematic structural view of Embodiment 5 and Embodiment 6 of the golf ball structure of the present invention.

參照第4圖,其為本創作利用「單心多殼」結構之態樣。如第4圖(A)部分所示,實施例五可為一層球心內層100與一層外層300。如第4圖(B)部分所示,實施例五可為一層球心內層100、一層中間層200與一層外層300。如第4圖(C)部分所示,實施例五可為一層球心內層100、兩層中間層200、201與一層外層300。此外,實施例五亦可為一層球心內層100、多層中間層200與一層外層300。Referring to Figure 4, it is a creation of a "single-hearted, multi-shell" structure. As shown in part (A) of Fig. 4, the fifth embodiment may be a layer of inner core layer 100 and an outer layer 300. As shown in part (B) of Fig. 4, the fifth embodiment may be a layer of inner core layer 100, an intermediate layer 200 and an outer layer 300. As shown in part (C) of Fig. 4, the fifth embodiment may be a layer of inner core layer 100, two intermediate layers 200, 201 and an outer layer 300. In addition, Embodiment 5 may also be a layer of inner core layer 100, a plurality of intermediate layers 200 and an outer layer 300.

參照第5圖,其為本創作利用「雙心多殼」結構之態樣。如第5圖(A)部分所示,實施例六可為兩層球心內層100、101與一層外層300。如第5圖(B)部分所示,實施例六可為兩層球心內層100、101、一層中間層200與一層外層300。如第5圖(C)部分所示,實施例六可為兩層球心內層100、101、兩層中間層200、201與一層外層300。此外,實施例六亦可為兩層球心內層100、101、多層中間層200與一層外層300。其中,兩層球心內層可利用兩次熱壓成型製得。較佳地,球心內層100的直徑可為20-25 mm,球心內層101的直徑可為5-11 mm。Referring to Figure 5, it is a creation of the "double-hearted and multi-shell" structure. As shown in part (A) of Fig. 5, the sixth embodiment may be a two-layer inner core layer 100, 101 and an outer layer 300. As shown in part (B) of Fig. 5, the sixth embodiment may be a two-layer inner core layer 100, 101, an intermediate layer 200 and an outer layer 300. As shown in part (C) of Fig. 5, the sixth embodiment may be two inner core layers 100, 101, two intermediate layers 200, 201 and one outer layer 300. In addition, the sixth embodiment may also be a two-layer inner core layer 100, 101, a plurality of intermediate layers 200 and an outer layer 300. Among them, the inner layer of the two layers of the core can be obtained by two hot press forming. Preferably, the inner core layer 100 may have a diameter of 20-25 mm, and the inner core layer 101 may have a diameter of 5-11 mm.

綜上所述,本創作之高爾夫球結構可依照不同的使用需求,調整含有的熱塑性聚氨酯組合物的成分,且本創作之高爾夫球結構,具有高操控性與耐用性等特點。In summary, the golf ball structure of the present invention can adjust the composition of the thermoplastic polyurethane composition contained according to different use requirements, and the golf ball structure of the present invention has high controllability and durability.

以上所述僅為舉例性,而非為限制性者。任何未脫離本創作之精神與範疇,而對其進行之等效修改或變更,均應包含於後附之申請專利範圍中。The above is intended to be illustrative only and not limiting. Any equivalent modifications or alterations to the spirit and scope of this creation shall be included in the scope of the appended patent application.

S11~S13、S21~S23、S31~S33、S40‧‧‧流程步驟
100、101‧‧‧球心內層
200、201‧‧‧中間層
300‧‧‧外層
S11~S13, S21~S23, S31~S33, S40‧‧‧ process steps
100, 101‧‧‧ inner core
200, 201‧‧‧ middle layer
300‧‧‧ outer layer

第1圖係為本創作之高爾夫球結構之熱塑性聚氨酯組合物的製備流程圖。Figure 1 is a flow chart for the preparation of a thermoplastic polyurethane composition of the golf structure of the present invention.

第2圖係為本創作之高爾夫球結構之實施例一的結構示意圖。Figure 2 is a schematic view showing the structure of the first embodiment of the golf ball structure of the present invention.

第3圖係為本創作之高爾夫球結構之實施例二的結構示意圖。Figure 3 is a schematic view showing the structure of the second embodiment of the golf ball structure of the present invention.

第4圖係為本創作之高爾夫球結構之實施例五的結構示意圖。Figure 4 is a schematic view showing the structure of the fifth embodiment of the golf ball structure of the present invention.

第5圖係為本創作之高爾夫球結構之實施例六的結構示意圖。Figure 5 is a schematic view showing the structure of the sixth embodiment of the golf ball structure of the present invention.

Claims (9)

一種高爾夫球結構,其包含: 一球心內層;以及 一外層,其包圍該球心內層,且包含一熱塑性聚氨酯組合物,該熱塑性聚氨酯組合物包含: 一第一聚氨酯,由一第一多異氰酸酯、一第一多元醇組合物以及一第一擴鏈劑組合物所組成; 一第二聚氨酯,由一第二多異氰酸酯、一第二多元醇組合物以及一第二擴鏈劑組合物所組成;以及 一第三聚氨酯,由一第三多異氰酸酯、一第三多元醇組合物以及一第三擴鏈劑組合物所組成; 其中,該第一多異氰酸酯、該第一多元醇組合物與該第一擴鏈劑組合物的莫耳數比為5:1:4; 其中,該第二多異氰酸酯、該第二多元醇組合物與該第二擴鏈劑組合物的莫耳數比為4:1:3; 其中,該第三多異氰酸酯、該第三多元醇組合物與該第三擴鏈劑組合物的莫耳數比為3:1:2。A golf ball structure comprising: a core inner layer; and an outer layer surrounding the inner core layer and comprising a thermoplastic polyurethane composition comprising: a first polyurethane, a first a polyisocyanate, a first polyol composition and a first chain extender composition; a second polyurethane comprising a second polyisocyanate, a second polyol composition and a second chain extender a composition of the composition; and a third polyurethane comprising a third polyisocyanate, a third polyol composition, and a third chain extender composition; wherein the first polyisocyanate, the first plurality The molar ratio of the polyol composition to the first chain extender composition is 5:1:4; wherein the second polyisocyanate, the second polyol composition and the second chain extender composition a molar ratio of 4:1:3; wherein the third polyisocyanate, the third polyol composition and the first Number of moles of the chain extender composition ratio of 3: 1: 2. 如申請專利範圍第1項所述之高爾夫球結構,其中該第一聚氨酯、該第二聚氨酯與該第三聚氨酯的重量比為20~60 份:10~50份:5~50 份。The golf ball structure according to claim 1, wherein the first polyurethane, the second polyurethane and the third polyurethane have a weight ratio of 20 to 60 parts: 10 to 50 parts: 5 to 50 parts. 如申請專利範圍第1項所述之高爾夫球結構,其中該第一多異氰酸酯、該第二多異氰酸酯以及該第三多異氰酸酯各自獨立地選自甲苯二異氰酸酯、二苯甲烷二異氰酸酯、六亞甲基二異氰酸酯、異佛爾酮二異氰酸酯或其組合。The golf ball structure of claim 1, wherein the first polyisocyanate, the second polyisocyanate, and the third polyisocyanate are each independently selected from the group consisting of toluene diisocyanate, diphenylmethane diisocyanate, and hexamethylene Diisocyanate, isophorone diisocyanate or a combination thereof. 如申請專利範圍第1項所述之高爾夫球結構,其中該第一多元醇組合物、該第二多元醇組合物以及該第三多元醇組合物各自獨立地選自聚酯、聚醚多元醇、聚酯多元醇或其組合。The golf ball structure of claim 1, wherein the first polyol composition, the second polyol composition, and the third polyol composition are each independently selected from the group consisting of polyester and poly Ether polyol, polyester polyol or a combination thereof. 如申請專利範圍第4項所述之高爾夫球結構,其中該第一多元醇組合物、該第二多元醇組合物以及該第三多元醇組合物各自獨立地選自聚丙烯酸丁酯、聚四氫呋喃或其組合。The golf ball structure of claim 4, wherein the first polyol composition, the second polyol composition, and the third polyol composition are each independently selected from polybutyl acrylate. , polytetrahydrofuran or a combination thereof. 如申請專利範圍第1項所述之高爾夫球結構,其中該第一擴鏈劑組合物、該第二擴鏈劑組合物以及該第三擴鏈劑組合物各自獨立地選自碳數C 1-C 5醇類、碳數C 1-C 5胺類、碳數C 1-C 5烷類或其組合。 The application of the golf ball structures patentable scope of item 1, wherein the first chain extender composition, the second chain extender composition and the third composition chain extender are each independently selected from C 1 carbon atoms a C 5 alcohol, a C 1 -C 5 amine, a C 1 -C 5 alkane or a combination thereof. 如申請專利範圍第6項所述之高爾夫球結構,其中該第一擴鏈劑組合物、該第二擴鏈劑組合物以及該第三擴鏈劑組合物各自獨立地選自丁二醇、乙二胺、三羥甲基丙烷或其組合。The golf ball structure of claim 6, wherein the first chain extender composition, the second chain extender composition, and the third chain extender composition are each independently selected from the group consisting of butanediol, Ethylenediamine, trimethylolpropane or a combination thereof. 如申請專利範圍第1項所述之高爾夫球結構,其中該熱塑性聚氨酯組合物更包含一聚醚胺組合物。The golf ball structure of claim 1, wherein the thermoplastic polyurethane composition further comprises a polyetheramine composition. 如申請專利範圍第8項所述之高爾夫球結構,其中該第一聚氨酯、該第二聚氨酯以及該第三聚氨酯的總重量與該聚醚胺組合物的重量的重量比為90~99份:1~10份。The golf ball structure of claim 8, wherein the weight ratio of the total weight of the first polyurethane, the second polyurethane, and the third polyurethane to the weight of the polyetheramine composition is 90 to 99 parts: 1~10 servings.
TW106216040U 2017-10-30 2017-10-30 Golf ball structure TWM556619U (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
TW106216040U TWM556619U (en) 2017-10-30 2017-10-30 Golf ball structure

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
TW106216040U TWM556619U (en) 2017-10-30 2017-10-30 Golf ball structure

Publications (1)

Publication Number Publication Date
TWM556619U true TWM556619U (en) 2018-03-11

Family

ID=62191360

Family Applications (1)

Application Number Title Priority Date Filing Date
TW106216040U TWM556619U (en) 2017-10-30 2017-10-30 Golf ball structure

Country Status (1)

Country Link
TW (1) TWM556619U (en)

Similar Documents

Publication Publication Date Title
JP4038625B2 (en) Solid golf ball and method for producing solid golf ball
CN202961731U (en) Solid golf ball
CN103002956B (en) There is the golf of ionomer/hydrophobic thermoplastic polyurethane layer
US20050176533A1 (en) Balls for use in baseball and softball
JP5258262B2 (en) Golf ball
CN104971472B (en) With center and the golf around sandwich layer outside foam
US20090280927A1 (en) Golf ball with head resistant shield layer
US20040254298A1 (en) Golf ball incorporating styrenic block copolymer and urethane
CN103702724B (en) Comprise golf and the preparation method of the blend of the acid polymer of highly neutralization
JP2009131508A (en) Golf ball
JP2011092328A (en) Golf ball resin composition and golf ball using the same
CN103781517B (en) Method of manufacturing a golf ball including a blend of highly neutralized acid polymers
US9352192B2 (en) Golf ball polyurethane composition and golf ball
CN102892468B (en) There is the golf of damp-proof layer
JP2012011202A (en) Golf ball incorporating thermoplastic polyurethane
US9314671B2 (en) Golf ball polyurethane composition and golf ball
JP5258263B2 (en) Golf ball
JP2011125438A (en) Golf ball material and golf ball using the same
CN110270065A (en) Golf with sandwich layer outside foaming inner core and thermosetting property
TWI641652B (en) Thermoplastic polyurethane composition and golf including the same
TWI649186B (en) Method of preparing golf ball
JP2009112649A (en) Golf ball
TWM556619U (en) Golf ball structure
JP5258363B2 (en) Golf ball
JP2017209297A (en) Golf ball