阅读说明：本技术 制造高尔夫球的方法及所得的高尔夫球 (Method of manufacturing a golf ball and resulting golf ball ) 是由 迈克尔·米歇尔沃驰 布莱恩·科莫 肖恩·里奇 于 2021-04-09 设计创作，主要内容包括：制造高尔夫球的方法包括提供子组件,围绕其形成至少一个由使用下述制备的预聚物产生的热固性聚氨酯构成的层：使化学计量过量的第一异氰酸酯与至少一种长链多元醇和/或多元胺软段反应,生成具有(％NCO)-(第一预聚物)的第一异氰酸酯封端的第一预聚物；将化学计量过量的另外的异氰酸酯加入前述物质中制备具有(％NCO)-(改性的第一预聚物)的改性的第一预聚物；其中(％NCO)-(改性的第一预聚物)＞(％NCO)-(第一预聚物)。在多个步骤使化学计量过量的异氰酸酯反应,并错开将总量游离、反应性和未反应异氰酸酯官能团加入异氰酸酯官能的最终预聚物,产生改进的最终预聚物及具有更好物理性能的所得热固性聚氨酯,其中总％NCO在单一步骤加入或直到完全加入预聚物形成过程中时才加入。(The method of making a golf ball includes providing a subassembly about which is formed at least one thermoset polyurethane produced using a prepolymer prepared as described belowLayer composed of ester: reacting a stoichiometric excess of a first isocyanate with at least one long chain polyol and/or polyamine soft segment to a composition having (% NCO) First prepolymer A first isocyanate terminated prepolymer of (a); preparation of a polyurethane foam having (% NCO) by adding a stoichiometric excess of additional isocyanate to the foregoing Modified first prepolymer The modified first prepolymer of (a); wherein (% NCO) Modified first prepolymer ＞(％NCO) First prepolymer . Reacting a stoichiometric excess of isocyanate in multiple steps and staggering the addition of the total amount of free, reactive, and unreacted isocyanate functional groups to the isocyanate functional final prepolymer yields an improved final prepolymer and resulting thermoset polyurethane with better physical properties, where the total% NCO is added in a single step or not until fully added to the prepolymer formation process.)

1. A method of manufacturing a golf ball comprising the steps of providing a subassembly, and forming at least one layer comprised of a thermoset polyurethane around the subassembly, the thermoset polyurethane being produced using a prepolymer prepared by the steps of:

(i) reacting a stoichiometric excess of a first isocyanate with at least one long chain polyol and/or polyamine soft segment to a composition having (% NCO)_{First prepolymer}A first isocyanate terminated prepolymer of (a);

(ii) adding a stoichiometric excess of additional isocyanate to the first isocyanate-terminated first prepolymer to produce a prepolymer having (% NCO)_{Modified first prepolymer}The modified first prepolymer of (a);

wherein, (% NCO)_{Modified first prepolymer}＞(％NCO)_{First prepolymer}。

2. The method of claim 1, wherein (% NCO)_{Modified first prepolymer}Is 7 or greater, (% NCO)_{First prepolymer}From 2 to less than 7.

3. The method of claim 1, wherein (% NCO)_{Modified first prepolymer}From 7 to 14, (% NCO)_{First prepolymer}From 2 to less than 7.

4. The method of claim 1, wherein (% NCO)_{Modified first prepolymer}Is 7 to 10, (% NCO)_{First prepolymer}Is 3 to 5.

5. The method of claim 2, wherein the first isocyanate and the additional isocyanate are the same.

6. The process of claim 5, wherein the first isocyanate and the additional isocyanate are each isophorone diisocyanate; and wherein the at least one long chain polyol and/or polyamine soft segment is polytetramethylene glycol having a molecular weight of 2000 g/mol.

7. The method of claim 2, wherein the first isocyanate and the additional isocyanate are different.

8. The method of claim 2, wherein the first isocyanate is included in an amount of 15% to 22% based on the total weight of the thermoset polyurethane formulation.

9. The method of claim 8, wherein the additional isocyanate is included in an amount of 0.5% to 15% based on the total weight of the thermoset polyurethane formulation.

10. The method of claim 9, wherein at least one layer is a cap formed around the subassembly by casting.

11. The method of claim 2, wherein the first isocyanate and the additional isocyanate are included in a weight ratio of 1:1 to 25: 1.

Technical Field

Methods of making golf balls incorporating the improved thermoset polyurethane materials and the resulting improved golf balls.

Disclosure of Invention

Thus, in the process of the present invention for making the resulting improved golf balls of the present invention, a stoichiometric excess of isocyanate is introduced in multiple steps during the preparation of the final prepolymer so that the total amount of isocyanate contributed is staggered (stagged) to produce a new prepolymer having a unique morphology, and this in turn will produce a new resulting thermoset polyurethane having improved physical properties such as tensile strength, tensile elongation at break, and energy at break.

In one embodiment, a method of making a golf ball includes the steps of providing a subassembly, and forming at least one layer comprised of a thermoset polyurethane around the subassembly, the thermoset polyurethane being produced using a prepolymer, the prepolymer being prepared by: (i) reacting a stoichiometric excess of a first isocyanate with at least one long chain polyol and/or polyamine soft segment (soft segment) to form a polyurethane foam having (% NCO)_{First prepolymer}A first isocyanate terminated prepolymer of (a); and (ii) adding a stoichiometric excess of additional isocyanate to the first isocyanateEster-terminated first prepolymer to make a prepolymer having (% NCO)_{Modified first prepolymer}The modified first prepolymer of (a); wherein (% NCO)_{Modified first prepolymer}＞(％NCO)_{First prepolymer}。

In one embodiment, (% NCO)_{Modified first prepolymer}Is 7 or greater, (% NCO)_{First prepolymer}From 2 to less than 7.

In another embodiment, (% NCO)_{Modified first prepolymer}From 7 to 14, (% NCO)_{First prepolymer}From 2 to less than 7.

In a particular embodiment, the first isocyanate and the further isocyanate are the same.

In a particular embodiment, the first isocyanate and the further isocyanate are each isophorone diisocyanate; and at least one of the long chain polyol and/or polyamine soft segment is polytetramethylene glycol (polytetramethylene glycol) having a molecular weight of 2000 g/mol.

In another particular embodiment, the first isocyanate and the additional isocyanate are different.

In a particular embodiment, the first isocyanate is present in an amount from about 15% to about 22% based on the total weight of the thermoset polyurethane formulation.

In another embodiment, the additional isocyanate is present in an amount of about 0.5% to about 15% based on the total weight of the thermoset polyurethane formulation.

In one embodiment, at least one layer is a cap formed around the subassembly by casting.

In a particular embodiment, the first isocyanate and the additional isocyanate are included in a weight ratio of 1:1 to 25: 1.

Drawings

Other features and advantages of the present invention can be determined from the following detailed description provided in conjunction with the following drawings described below:

FIG. 1 is a schematic diagram showing first and second reaction steps for preparing a modified first prepolymer according to one embodiment of the present invention.

Detailed Description

Advantageously, in the process of the present invention for making the resulting improved golf ball of the present invention, a stoichiometric excess of isocyanate is introduced in multiple steps, wherein the total amount of isocyanate added during the preparation of the final prepolymer is staggered, thereby producing an improved thermoset polyurethane with better physical properties.

Accordingly, in one embodiment, a method of making a golf ball includes the steps of providing a subassembly, and forming at least one layer comprised of a thermoset polyurethane around the subassembly, the thermoset polyurethane being produced using a prepolymer, the prepolymer being prepared by the steps of: (i) reacting a stoichiometric excess of a first isocyanate with at least one long chain polyol and/or polyamine soft segment to form a polyurethane having (% NCO)_{First prepolymer}A first isocyanate terminated prepolymer of (a); and (ii) adding a stoichiometric excess of additional isocyanate to the first isocyanate-terminated first prepolymer to produce a prepolymer having (% NCO)_{Modified first prepolymer}The modified first prepolymer of (a); wherein (% NCO)_{Modified first prepolymer}＞(％NCO)_{First prepolymer}。

The additional isocyanate provided in step (ii) dilutes the first prepolymer, increasing the% NCO, but does not otherwise react with the first prepolymer. In fact, as shown in tables I and II below, by producing a polycarbonate having a relatively low (% NCO)_{First prepolymer}Followed by dilution of the first prepolymer to yield a prepolymer having a relatively high (% NCO)_{Modified first prepolymer}To produce a modified first prepolymer having a larger M than a conventional prepolymer in which the same total% NCO (produced using conventional prepolymer processes) is added in a single step_n(number average molecular weight), M_w(weight average molecular weight) and Z weight average molecular weight (M)_z)。

Furthermore, as shown in table III below, these improvements in the novel prepolymer translate into better physical properties of the resulting thermoset polyurethane polymer ("polymer") of the present invention, such as tensile strength at break, energy at break, and% elongation at break, as compared to conventional thermoset polyurethanes.

The term "percent NCO" or "% NCO" as used herein refers to the weight percentage of free, reactive, and unreacted isocyanate functional groups in the isocyanate functional first prepolymer and/or modified first prepolymer. Thus, the total formula weight of all NCO groups in the first prepolymer divided by its total molecular weight and multiplied by 100 equals (% NCO)_{First prepolymer}(ii) a And the total formula weight of all NCO groups in the modified prepolymer divided by its total molecular weight and multiplied by 100 equals (% NCO)_{Modified first prepolymer}。

By reacting a stoichiometric excess of isocyanate in multiple steps during the preparation of the final "modified first prepolymer", the total amount of free, reactive and unreacted isocyanate functional groups in the isocyanate functional final prepolymer are staggered to improve not only the final prepolymer but also the physical properties of the thermoset polyurethane material.

The number of unreacted NCO groups in the first prepolymer and the modified prepolymer can be, for example, as disclosed herein with respect to (% NCO)_{First prepolymer}And (% NCO)_{Modified first prepolymer}To control factors such as reaction speed, hardness of the resulting thermosetting polyurethane, etc. in the resulting final prepolymer. In general, prepolymers based on isocyanates having higher functionality may have higher viscosities, while prepolymers having higher NCO contents generally have lower viscosities.

In one embodiment of the process of the present invention, (% NCO)_{Modified first prepolymer}Is 7 or greater, (% NCO)_{First prepolymer}From 2 to less than 7. In one specific such embodiment, (% NCO)_{Modified first prepolymer}From 7 to about 14, (% NCO)_{First prepolymer}From about 2 to less than 7. In another embodiment, (% NCO)_{Modified first prepolymer}Is 7-10, (% NCO)_{First prepolymer}Is about 4. In yet another embodiment, (% NCO)_{Modified first prepolymer}Is 7-10, (% NCO)_{First prepolymer}Is 3-5.

In an alternative embodiment, (% NCO)_{Modified first prepolymer}May be about 7.5 or greater, or about 8 or greater, or 8.0 or greater, or about 9 or greater, or 9.0 or greater, or 10.0 or greater, or 12.0 or greater, or 15.0 or greater, or 17.0 or greater, or 20.0 or greater, or 22.0 or greater, or 25.0 or greater, or 30.0 or greater, or 7 to about 35, or 7 to 35, or about 7.5 to about 30, or 7.5 to 30, or 7.0 to about 25, or 7.0 to about 20, or 7.0 to about 15.

Meanwhile, (% NCO)_{First prepolymer}Alternatively may be 2.0 to 6.5, or 2.0 to 6.0, or 2.0 to 5.5, or 2.0 to 5.0, or 2.0 to 4.5, or 2.0 to 4.0, or 2.0 to 3.5, or 2.0 to 3.0, or 3.0 to less than 7.0, or 3.0 to 6.5, or 3.0 to 6.0, or 3.0 to 5.5, or 3.0 to 5.0, or 3.0 to 4.5, or 3.0 to 4.0, or 3.0 to 3.5, or 4.0 to less than 7.0, or 4.0 to 6.5, or 4.0 to 6.0, or 4.0 to 5.0, or 6.0, or 5.0 to 6.5.5.

In a specific embodiment, (% NCO)_{Modified first prepolymer}：(％NCO)_{First prepolymer}The ratio of (a) may be 7:4, or 6-8:3-5, or about 6-8: 3-5.

Thus, there is a change or delta (Δ) in the% unreacted NCO groups between the first prepolymer and the modified first prepolymer. For example, the change in% unreacted NCO groups between the first prepolymer and the modified first prepolymer can be +2 or greater, or about +2 or greater, or +3 or greater, or about +3 or greater, or +4 or greater, or about +4 or greater, or +5 or greater, or about +5 or greater, or +6 or greater, or about +6 or greater, or +7 or greater, or about +7 or greater.

In particular embodiments, the change in% unreacted NCO groups, or delta (Δ), between the first prepolymer and the modified first prepolymer can be from +2 to +20, or from +3 to +15, or from +4 to +10, or from +3 to + 7.

In a particular embodiment, the first isocyanate and the further isocyanate are the same.

In a particular embodiment, the first isocyanate and the further isocyanate are each isophorone diisocyanate; and at least one long-chain polyol and/or polyamine soft segment is polytetramethylene glycol having a molecular weight of 2000 g/mol.

In another particular embodiment, the first isocyanate and the additional isocyanate are different.

In a particular embodiment, the first isocyanate is present in an amount from about 15% to about 22% based on the total weight of the thermoset polyurethane formulation. In other such embodiments, the first isocyanate is included in an amount of 15% to 22%, or about 17% to about 20%, or 17% to 20%, based on the total weight of the formulation of the thermoset polyurethane.

In another particular embodiment, the additional isocyanate may be included in an amount of about 0.5% to about 15% based on the total weight of the formulation of the thermoset polyurethane. In other such embodiments, the additional isocyanate may be included in an amount of 0.5% to 15%, or about 1.5% to about 13%, or 1.5% to 13%, or about 3.0% to about 10%, or 3.0% to 10%, or about 5% to about 7%, or about 5% to about 15%, or 5% to 15%, based on the total weight of the formulation of the thermoset polyurethane.

In one embodiment, at least one layer is a cap formed around the subassembly by casting.

In a particular embodiment, the first isocyanate and the additional isocyanate are included in a weight ratio of 1:1 to 25: 1. In other particular embodiments, the first isocyanate and the additional isocyanate may be included in a weight ratio of 1:1 to 5:4, or 1:1 to 5:3, or 1:1 to 5:2, or 1:1 to 5:1.

Unexpectedly, as demonstrated by the results set forth in tables I, II and III and the accompanying discussion below, excellent castable thermoset polyurethane materials of the present invention, e.g., PU example 1, can be prepared with better physical properties, such as tensile strength at break, energy at break, and elongation at break, due to the number average molecular weight (M.sup.m) of modified first prepolymer example 1 of the present invention as compared to conventional thermoset polyurethane PU comparative example 1 prepared using conventional prepolymer method and conventional prepolymer comparative example 1_n) Weight average molecular weight (M)_w) Z weight average molecular weight (M)_z) Is biggerBut with the same final total% NCO.

Referring to table I, modified first prepolymer example 1 of the present invention was prepared according to the process of the present invention and compared to conventional prepolymer comparative example 1 prepared using conventional prepolymer process (I) as further identified above. That is, modified first prepolymer example 1 of the present invention was prepared by reacting PTMEG 2000 with a stoichiometric excess of isophorone diisocyanate (IPDI) at 4% NCO in a reaction vessel/flask. It is allowed to react and exotherm to about 80-90 ℃ and then held for about one hour, followed by cooling to produce the first prepolymer. Subsequently, an additional amount of IPDI was added after the first prepolymer addition in the flask/vessel, reacted and exothermed to about 80 deg.C-90 deg.C, then held for about one hour, then cooled to yield a modified first prepolymer example 1 comprising a final 7% NCO. The post-addition isocyanate IPDI does not interact with the initial prepolymer, except for the dilution and addition of more% NCO.

In contrast, conventional prepolymer comparative example 1 was prepared by reacting PTMEG 2000 with a stoichiometric excess of IPDI at 7% NCO in a reaction vessel/flask, allowing it to react and exotherm to about 80 ℃ to 90 ℃, then held for about one hour, then cooled to produce conventional prepolymer comparative example 1, without post-addition of isocyanate.

PTMEG 2000 is a polyether diol based on polytetramethylene ether glycol.

In this regard, the number average molecular weight (M) of each of the resulting modified first prepolymers of example 1 and conventional comparative example 1 was_n) Weight average molecular weight (M)_w) Z weight average molecular weight (M)_z) And Polydispersity (PD) as shown in table II below.

Number average molecular weight (M)_n) Weight average molecular weight (M)_w) Z weight average molecular weight (M)_z) Can be determined by gel permeation chromatography using polystyrene as a standard, as known in the art, and is described, for example, in U.S. Pat. No. 4,739,019 at column 4, 2-45Discussed in the lines, which are incorporated herein by reference in their entirety. Meanwhile, the Polydispersity (PD) can be calculated as: PD-Mw/Mn.

Subsequently, each of modified first prepolymer example 1 of the present invention and conventional prepolymer comparative example 1 was combined with the same chain extender, i.e., diethyltoluenediamine (DETDA) ((DETDA))100) With the same NCO: NH₂Ratio (1.05:1.0) to prepare thermosetting polyurethane PU example 1 of the present invention and conventional thermosetting polyurethane PU comparative example 1, respectively.

Next, the resulting physical properties of PU example 1 and PU comparative example 1 were evaluated to test and confirm the advantages of PU example 1 of the present invention compared with conventional PU comparative example 1. Specifically, therefore, the tensile strength at break, the energy at break and the elongation at break of each of the resulting materials of PU example 1 and PU comparative example 1 were evaluated in accordance with ASTM D-412, and the results are shown in the following Table III:

in this regard, Table III reveals that thermoset polyurethane PU example 1 of the present invention desirably has a tensile strength at break of 3800psi, 150psi greater than the tensile strength at break (3650) of comparative example 1, which is a comparative conventional material PU. Meanwhile, the thermosetting polyurethane PU example 1 of the present invention desirably has a fracture energy of 279in lbf, which is 34in lbf higher than that of comparative material PU comparative example 1(255in lbf), which is significant, if not moderate, as evidenced by a greater increase in tensile strength at break relative to that of comparative material PU comparative example 1. And the result was achieved while increasing the elongation% (523) of PU example 1 by 27 percentage points compared to the elongation% (496) of PU comparative example 1.

Thus, new and improved prepolymers and resulting thermoset polyurethane materials can be produced by the process of the present invention wherein a stoichiometric excess of isocyanate is added in a stepwise (step-wise) and staggered manner throughout the prepolymer formation process, rather than being added all to the system in a single step and/or remaining added to the prepolymer system until after the first formation of the polyamine or hydroxyl terminated prepolymer.

The golf balls of the present invention may have many different configurations, such as where the golf balls have a solid or multi-layer rubber core, an ionomer or other thermoplastic layer, and a cast thermoset cover layer made from the prepolymer of the present invention and a post-addition. The prepolymer containing the post addition may be made from one isocyanate or a blend of isocyanates. The isocyanate used to prepare the prepolymer may be the same or different from the isocyanate used as the post-addition isocyanate.

The term "isocyanate" as used herein refers to any aliphatic or aromatic isocyanate containing two or more isocyanate functional groups. The isocyanate compounds may be monomeric or monomeric units in that they may be polymerized to produce a polymeric isocyanate containing two or more monomeric isocyanate repeat units. The isocyanate compound may have any suitable backbone structure, including saturated or unsaturated, and linear, branched, or cyclic. The term "isocyanate" as used herein includes all isocyanate/diisocyanate compounds disclosed herein as well as other isocyanates.

The term "polyol" as used herein generally refers to any aliphatic or aromatic compound containing two or more hydroxyl functional groups. The term "polyol" may be used interchangeably with hydroxyl terminated component.

The term "polyamine" as used herein generally refers to any aliphatic or aromatic compound containing two or more primary or secondary amine functional groups. The polyamine compounds can have any suitable backbone structure, including saturated or unsaturated, and linear, branched, or cyclic. The term "polyamine" may be used interchangeably with the phrase amine-terminated component.

In addition to polyols having hydroxyl end groups, it is contemplated that the polyols may contain carboxyl, amino or mercapto end groups.

Polyester polyols can be prepared by reacting a dicarboxylic acid with a diol or an ester-forming derivative thereof. Examples of suitable dicarboxylic acids include succinic acid, glutaric acid, adipic acid, suberic acid, azelaic acid, sebacic acid, decanedicarboxylic acid, maleic acid, fumaric acid, phthalic acid, isophthalic acid and terephthalic acid. Examples of suitable diols include ethylene glycol, diethylene glycol, 1, 2-and 1, 3-propanediol, dipropylene glycol, 1, 4-butanediol, 1, 5-pentanediol, 1, 6-hexanediol, 1, 10-decanediol, glycerol and trimethylolpropane, tripropylene glycol, tetraethylene glycol, tetrapropylene glycol, tetramethylene glycol, 1, 4-cyclohexane-dimethanol. In practice, both the dicarboxylic acid and the diol may be used alone or as a mixture in the preparation of the particular polyester. Examples of suitable polyester polyols include, but are not limited to, polyethylene adipate, polybutylene adipate, polypropylene adipate, phthalate-1, 6-hexanediol, and combinations thereof.

Polyether polyols can be prepared by ring-opening addition polymerization of alkylene oxides with polyol polymerization initiators. Examples of suitable polyether polyols are polypropylene glycol (PPG), polyethylene glycol (PEG), polytetramethylene ether glycol (PTMEG). In addition, block copolymers such as polyoxypropylene and polyoxyethylene glycols, poly-1, 2-oxybutylene and polyoxyethylene glycols, poly-1, 4-tetramethylene and polyoxyethylene glycols.

Polycarbonate polyols can be prepared by denaturing reactions (degenerative reactions) of diols with phosgene, chloroformates, dialkyl carbonates and/or diallyl carbonate. Examples of diols in suitable polycarbonate polyols for crosslinking thermoplastic polyurethane elastomers include ethylene glycol, diethylene glycol, 1, 3-butanediol, 1, 4-butanediol, 1, 6-hexanediol, neopentyl glycol and 1, 5-pentanediol. One suitable polycarbonate includes, but is not limited to, a polyterephthalate carbonate.

Suitable polycaprolactone polyols include, but are not limited to, 1, 6-hexanediol initiated polycaprolactone, diethylene glycol initiated polycaprolactone, trimethylolpropane initiated polycaprolactone, neopentyl glycol initiated polycaprolactone, 1, 4-butanediol initiated polycaprolactone, and combinations thereof.

The polyol may be selected, for example, from the group consisting of: ethylene glycol; diethylene glycol; polyethylene glycol; propylene glycol; polypropylene glycol; lower molecular weight polytetramethylene ether glycol; 1, 3-bis (2-hydroxyethoxy) benzene; 1, 3-bis- [2- (2-hydroxyethoxy) ethoxy ] benzene; 1, 3-bis- {2- [2- (2-hydroxyethoxy) ethoxy ] ethoxy } benzene; 1, 4-butanediol; 1, 5-pentanediol; 1, 6-hexanediol; resorcinol-bis (β -hydroxyethyl) ether; hydroquinone-di (β -hydroxyethyl) ether; trimethylolpropane; and combinations thereof.

Polyamines may include, for example: 3, 5-dimethylthio-2, 4-toluenediamine, or isomers thereof; 3, 5-diethyltoluene-2, 4-diamine, or an isomer thereof; 4,4' -bis- (sec-butylamino) -diphenylmethane; 1, 4-bis- (sec-butylamino) -benzene, 4,4' -methylene-bis- (2-chloroaniline); 4,4' -methylene-bis- (3-chloro-2, 6-diethylaniline); trimethylene glycol-di-p-aminobenzoate; polytetrahydrofuran-di-p-aminobenzoate; n, N' -dialkyldiaminodiphenylmethane; p, p' -methylenedianiline; phenylenediamine; 4,4' -methylene-bis- (2-chloroaniline); 4,4' -methylene-bis- (2, 6-diethylaniline); 4,4' -diamino-3, 3' -diethyl-5, 5' -dimethyldiphenylmethane; 2,2',3,3' -tetrachlorodiaminodiphenylmethane; 4,4' -methylene-bis- (3-chloro-2, 6-diethylaniline); and 4,4' -diaminobenzene, or isomers thereof; 3,3' -diaminodiphenyl sulfone, or an isomer thereof; and combinations thereof.

Polyamines may also include, but are not limited to: 3, 5-dimethylthio-2, 4-toluenediamine and isomers thereof; 3, 5-diethyltoluene-2, 4-diamine and isomers thereof, such as 3, 5-diethyltoluene-2, 6-diamine; 4,4' -bis- (sec-butylamino) -diphenylmethane; 1, 4-bis- (sec-butylamino) -benzene, 4,4' -methylene-bis- (2-chloroaniline); 4,4' -methyleneBis- (3-chloro-2, 6-diethylaniline); polytetrahydrofuran-di-p-aminobenzoate; n, N' -dialkyldiaminodiphenylmethane; p, p' -methylenedianiline ("MDA"); metaphenylene diamine ("MPDA"); 4,4' -methylene-bis- (2-chloroaniline) ("MOCA"); 4,4' -methylene-bis- (2, 6-diethylaniline); 4,4' -diamino-3, 3' -diethyl-5, 5' -dimethyldiphenylmethane; 2,2',3,3' -tetrachlorodiaminodiphenylmethane; 4,4' -methylene-bis- (3-chloro-2, 6-diethylaniline); trimethylene glycol di-p-aminobenzoate; and combinations thereof. Preferably, the curing agent comprises 3, 5-dimethylthio-2, 4-toluenediamine and isomers thereof, e.g.300. Suitable polyamine curing agents, including primary and secondary amines, preferably have a weight average molecular weight of about 64 to about 2000.

Suitable diol, triol and tetraol groups include: ethylene glycol; diethylene glycol; polyethylene glycol; propylene glycol; polypropylene glycol; lower molecular weight polytetramethylene ether glycol; 1, 3-bis (2-hydroxyethoxy) benzene; 1, 3-bis- [2- (2-hydroxyethoxy) ethoxy ] benzene; 1, 3-bis- {2- [2- (2-hydroxyethoxy) ethoxy ] ethoxy } benzene; 1, 4-butanediol; 1, 5-pentanediol; 1, 6-hexanediol; resorcinol-bis (4-hydroxyethyl) ether; hydroquinone-bis (4-hydroxyethyl) ether; and combinations thereof. Preferred hydroxyl terminated curing agents include ethylene glycol; diethylene glycol; 1, 4-butanediol; 1, 5-pentanediol; 1, 6-hexanediol, trimethylolpropane, and combinations thereof. Preferably, the hydroxyl terminated curing agent has a molecular weight of about 48 to 2000. As used herein, molecular weight is the absolute weight average molecular weight, and will be so understood by those of ordinary skill in the art.

Both the hydroxyl terminated and amine chain extenders can include one or more saturated, unsaturated, aromatic and cyclic groups. In addition, the hydroxyl terminated curing agent and the amine curing agent may include one or more halogen groups. While a single chain extender (chain extending agent) may be used, blends or mixtures of chain extenders may also be used if desired.

Catalysts are also sometimes used to promote the reaction between the isocyanate and polyol compounds to produce the prepolymer, or the reaction between the prepolymer and the curative during the chain extension step. The catalyst is typically added to the reactants prior to making the prepolymer. Examples of such catalysts include: a bismuth catalyst; zinc octoate; stannous octoate; tin catalysts, such as dibutyltin dilaurate, dibutyltin diacetate, stannous octoate; tin (II) chloride, tin (IV) chloride, dibutyl tin dimethoxy, dimethyl-bis [ 1-oxadecyl) oxy ] stannane, di-n-octyl tin di-isooctyl mercaptoacetate; amine catalysts such as triethylenediamine, triethylamine, and tributylamine; organic acids such as oleic acid and acetic acid; a delayed catalyst; and mixtures thereof. The catalyst is preferably added in an amount sufficient to catalyze the reaction of the components of the reaction mixture, for example in an amount of from about 0.001% to about 1%, preferably from 0.1 to 0.5%, by weight of the composition.

Examples of hydroxyl terminated chain extenders are generally selected from the group consisting of: ethylene glycol; diethylene glycol; polyethylene glycol; propylene glycol; 2-methyl-1, 3-propanediol; 2-methyl-1, 4-butanediol; monoethanolamine; diethanolamine; triethanolamine; monoisopropanolamine; diisopropanolamine; dipropylene glycol; 1, 2-butanediol; 1, 3-butanediol; 1, 4-butanediol; 2, 3-butanediol; 2, 3-dimethyl-2, 3-butanediol; trimethylolpropane; a cyclohexyl dimethylol group; triisopropanolamine; n, N' -tetrakis- (2-hydroxypropyl) -ethylenediamine; diethylene glycol bis (aminopropyl) ether; 1, 5-pentanediol; 1, 6-hexanediol; 1, 3-bis- (2-hydroxyethoxy) cyclohexane; 1, 4-cyclohexyl dimethylol; 1, 3-bis- [2- (2-hydroxyethoxy) ethoxy]Cyclohexane; 1, 3-bis- {2- [2- (2-hydroxyethoxy) ethoxy]Ethoxy } -cyclohexane; trimethylolpropane; polytetramethylene ether glycol (PTMEG), preferably having a molecular weight of about 250 to about 3900; and mixtures thereof. In addition, the following hydroxyl-terminated curing agents may be used: 1, 7-heptanediol, 1, 8-octanediol, 1, 9-nonanediol, 1, 10-decanediol, 1, 11-undecanediol, and 1, 12-dodecanediol. However, it is not required in the process of the present invention to use only linear hydroxyl-terminated curing agents containing 1 to 12 carbon atoms. For example, linear hydroxyl-terminated curing agents containing greater than 12 carbon atoms, such as tetradecanoic acid (C), can be used₁₄) Diol, hexadecanoic acid (C)₁₆) Diols and octadecanoic acid (C)₁₈) A diol. Furthermore, alkyl or aryl substituted alkane diols containing more than 12 carbon atoms may be used. As mentioned above, the characteristics of the polyurethane composition depend to a large extent on the components or structural units used to prepare the composition, in particular the polyisocyanate of the present invention, the moisture-resistant polyol and the curing agent. The above-described hydroxyl-terminated curing agents are useful in the preparation of polyurethane compositions having improved tensile strength, impact durability, scuff/wear resistance, resilience, and moisture resistance.

Suitable amine-terminated chain extenders useful for chain extending the polyurethane prepolymers of the present invention include, but are not limited to: unsaturated diamines, such as 4,4' -diamino-diphenylmethane (i.e. 4,4' -methylenedianiline or "MDA"), m-phenylenediamine, p-phenylenediamine, 1, 2-or 1, 4-bis (sec-butylamino) benzene, 3, 5-diethyl- (2, 4-or 2,6-) toluenediamine or "DETDA", 3, 5-dimethylthio- (2, 4-or 2,6-) toluenediamine, 3, 5-diethylthio- (2, 4-or 2,6-) toluenediamine, 3' -dimethyl-4, 4' -diamino-diphenylmethane, 3' -diethyl-5, 5' -dimethyl-4, 4' -diamino-diphenylmethane (i.e. 4,4 '-methylene-bis (2-ethyl-6-methyl-benzylamine)), 3' -dichloro-4, 4 '-diamino-diphenylmethane (i.e., 4' -methylene-bis (2-chloroaniline) or "MOCA"), 3',5,5' -tetraethyl-4, 4 '-diamino-diphenylmethane (i.e., 4' -methylene-bis (2, 6-diethylaniline), 2 '-dichloro-3, 3',5,5 '-tetraethyl-4, 4' -diamino-diphenylmethane (i.e., 4 '-methylene-bis (3-chloro-2, 6-diethyleneaniline) or "MCDEA"), 3' -diethyl-5, 5 '-dichloro-4, 4' -diamino-diphenylmethane or "MDEA"), 3,3 '-dichloro-2, 2',6,6 '-tetraethyl-4, 4' -diamino-diphenylmethane, 3,3 '-dichloro-4, 4' -diamino-diphenylmethane, 4 '-methylene-bis (2, 3-dichloroaniline) (i.e., 2',3,3 '-tetrachloro-4, 4' -diamino-diphenylmethane or "MDCA"), 4 '-bis (sec-butylamino) -diphenylmethane, N' -dialkylamino-diphenylmethane, trimethylene glycol-bis (p-aminobenzoate), polyethylene glycol-bis (p-aminobenzoate) Polytetramethylene glycol-di(s) ((s))P-aminobenzoate); saturated diamines, e.g. ethylenediamine, 1, 3-propylenediamine, 2-methyl-pentylenediamine, hexamethylenediamine, 2, 4-and 2,4, 4-trimethyl-1, 6-hexamethylenediamine, iminobis (propylamine), methyliminobis (propylamine), i.e. N- (3-aminopropyl) -N-methyl-1, 3-propylenediamine, 1, 4-bis (3-aminopropoxy) butane, i.e. 3,3' [1, 4-butanediylbis- (oxy) bis (oxy)]-1-propylamine), diethylene glycol bis (propylamine) (i.e. diethylene glycol-bis (aminopropyl) ether), 4,7, 10-triacetamide-1, 13-diamine, 1-methyl-2, 6-diamino-cyclohexane, 1, 4-diamino-cyclohexane, poly (oxyethylene-oxypropylene) diamine, 1, 3-or 1, 4-bis (methylamino) -cyclohexane, isophoronediamine, 1, 2-or 1, 4-bis (sec-butylamino) -cyclohexane, N ' -diisopropyl-isophoronediamine, 4' -diamino-dicyclohexylmethane, 3' -dimethyl-4, 4' -diamino-dicyclohexylmethane, 3' -dichloro-4, 4 '-diamino-dicyclohexylmethane, N' -dialkylamino-dicyclohexylmethane, polyoxyethylenediamine, 3 '-diethyl-5, 5' -dimethyl-4, 4 '-diamino-dicyclohexylhan, polyoxypropylene diamine, 3' -diethyl-5, 5 '-dichloro-4, 4' -diamino-dicyclohexylmethane, polytetramethylene ether diamine, 3',5,5' -tetraethyl-4, 4 '-diamino-dicyclohexylmethane (i.e., 4' -methylene-bis (2, 6-diethylaminocyclohexane)), 3 '-dichloro-4, 4' -diamino-dicyclohexylmethane, poly (ethylene oxide-co-ethylene-co-ethylene-co-ethylene), poly (ethylene-co-ethylene-co-ethylene), poly (co-ethylene-co-ethylene-co-ethylene-co-ethylene-co-ethylene, co-ethylene-co-ethylene, co-ethylene-co-ethylene, co-ethylene-co-ethylene, co-ethylene, co-ethylene, co-ethylene, co-ethylene, co-ethylene, co-ethylene, co-ethylene, co-ethylene, co-ethylene, co, 2,2 '-dichloro-3, 3',5,5 '-tetraethyl-4, 4' -diamino-dicyclohexylmethane, (ethylene oxide) -capped polyoxypropylene ether diamine, 2',3,3' -tetrachloro-4, 4 '-diamino-dicyclohexylmethane, 4' -bis (sec-butylamino) -dicyclohexylmethane; triamines, e.g. diethylenetriamine, dipropylenetriamine, (propylene oxide) triamine (i.e. polyoxypropylene triamine), N- (2-aminoethyl) -1, 3-propanediamine (i.e. N₃-amines), glyceryl triamines, (fully saturated); tetraamines, e.g. N, N' -bis (3-aminopropyl) ethylenediamine (i.e. N)₄-amines) (homo-saturated), triethylenetetramine; and other polyamines, such as tetraethylenepentamine (also saturated). Amine chain extenders used as chain extenders typically have cyclic structures and low molecular weights (250 or less). More preferably, the amine terminated chain extender may be selected from: 1, 3-propanediamine, 1, 4-butanediamine, 1, 5-pentanediamine, 1, 6-hexanediamine, 1, 7-heptanediamine, 1, 8-octanediamine, 1, 9-nonanediamineAmines, 1, 10-decamethylenediamine, 1, 11-undecanediamine and 1, 12-dodecanediamine, polymethylene-di-p-aminobenzoate, polyethylene glycol-bis (4-aminobenzoate), polytetramethylene ether glycol-di-p-aminobenzoate, polypropylene glycol-di-p-aminobenzoate, and mixtures thereof.

Polyamide chain extenders having a polyamino group capable of reacting with isocyanate groups and at least one amide group are also used. Polyamine polyamides can be used wherein the polyamide chains are formed from the polycondensation reaction of a polyacid (including polyacid telechelics) and a polyamine (including polyamine telechelics) wherein the equivalent ratio of polyamine to polyacid is greater than 1, for example from about 1.1 to 5 or about 2. The mixture of polyacid and polyamine may be, for example, hexamethylenediammonium adipate, hexamethylenediammonium terephthalate or tetramethylenediammonium adipate. Alternatively, the polyamide chains may be formed in part or substantially by ring-opening polymerization of a cyclic amide, such as caprolactam. The polyamide chains may also be formed in part or substantially by the polymerization of amino acids, including those corresponding in structure to cyclic amides. The polyamide chain may comprise multiple segments formed from the same or different polyacids, polyamines, cyclic amides and/or amino acids, non-limiting examples of which are disclosed herein. Suitable starting materials also include polyacid polymers, polyamine telechelics, and amino acid polymers. At least one polyacid, polyamine, cyclic amide, or amino acid having a Mw of at least about 200, such as at least about 400, or at least about 1,000, can be used to form the backbone. Blends of at least two polyacids and/or blends of at least two polyamines, one of which has a higher molecular weight than the other, may be used. The lower molecular weight polyacids or polyamines can contribute to the hard segments in the polyamine polyamides, which can improve the shear resistance of the resulting elastomers. For example, the first polyacid/polyamine may have a molecular weight of less than 2,000 and the second polyacid/polyamine may have a molecular weight of 2,000 or greater. In one example, the polyamine blend can include a first polyamine having a Mw of 1,000 or less, such as jeffamine.400(Mw about 400), and a second polyamine having a Mw of 1,500 or greater, such as JEFFAMINE 2000(Mw about 2,000). The backbone of the polyamine polyamide can have from about 1 to about 100 amide linkages, such as from about 2 to about 50 or from about 2 to about 20. The polyamine polyamide can be linear, branched, star-shaped, hyperbranched, or dendritic (e.g., the amine-terminated hyperbranched quinoxaline amide polymer of U.S. patent 6,642,347, the disclosure of which is incorporated herein by reference).

The diamine may comprise an aliphatic, alicyclic or aromatic diamine.

Other examples of diamines include 1, 4-cyclohexanediamine, benzidine, toluenediamine, diaminodiphenylmethane, isomers of phenylenediamine and/or hydrazine, (4,4 '-methylene-bis-o-chloroaniline) and/or (4,4' -methylenebis (3-chloro-2, 6-diethyl-aniline).

Suitable isocyanates include, for example, those selected from the group consisting of: 4,4 '-diphenylmethane diisocyanate, polymeric 4,4' -diphenylmethane diisocyanate, carbodiimide-modified liquid 4,4 '-diphenylmethane diisocyanate, 4' -dicyclohexylmethane diisocyanate, p-phenylene diisocyanate, toluene diisocyanate, isophorone diisocyanate, p-methyl xylene diisocyanate, m-methyl xylene diisocyanate, o-methyl xylene diisocyanate, and combinations thereof.

Suitable polyisocyanates include, but are not limited to, 4 '-diphenylmethane diisocyanate ("MDI"), polymeric MDI, carbodiimide-modified liquid MDI, 4' -dicyclohexylmethane diisocyanate ("H)₁₂MDI "), p-phenylene diisocyanate (" PPDI "), toluene diisocyanate (" TDI "), 3 '-dimethyl-4, 4' -biphenylene diisocyanate (" TODI "), isophorone diisocyanate (" IPDI "), hexamethylene diisocyanate (" HDI "), naphthalene diisocyanate (" NDI "); xylene diisocyanate ("XDI"); p-tetramethylxylene diisocyanate ("p-TMXDI"); m-tetramethylxylene diisocyanate ("m-TMXDI"); ethylene diisocyanate; propylene-1, 2-diisocyanate; tetramethylene-1, 4-diisocyanate; cyclohexyl diisocyanate; 1, 6-hexamethylene-diisocyanate ("HDI"); dodecane-1, 12-diisocyanate; cyclobutane-1, 3-diisocyanate; cyclohexane-1, 3-diisocyanate; cyclohexane-1, 4-diisocyanate; 1-isocyanato-3, 3, 5-trimethyl-5-isocyanatomethylCyclohexane; methylcyclohexylene diisocyanate; triisocyanates of HDI; triisocyanates of 2,4, 4-trimethyl-1, 6-hexane diisocyanate ("TMDI"), tetracene diisocyanate, naphthalene diisocyanate, anthracene diisocyanate; and combinations thereof. Polyisocyanates are known to those of ordinary skill in the art and have more than one isocyanate group, such as di-, tri-, and tetra-isocyanates. Preferably, the polyisocyanate is selected from the group consisting of MDI, PPDI, TDI, and combinations thereof. More preferably, the polyisocyanate comprises MDI. It is to be understood that the term "MDI" as used herein includes 4,4' -diphenylmethane diisocyanate, polymeric MDI, carbodiimide modified liquid MDI, combinations thereof, and further that the diisocyanate used may be a "low free monomer" which is understood by those of ordinary skill in the art to have a lower level of "free" monomeric isocyanate groups than conventional diisocyanates, i.e., the compositions of the present invention typically have less than about 0.1% free monomeric groups. Examples of "low free monomer" diisocyanates include, but are not limited to, low free monomer MDI, low free monomer TDI, and low free monomer PPDI.

The at least one polyisocyanate may, for example, have about 18% or less unreacted NCO groups. In some embodiments, the at least one polyisocyanate has no more than 8.5% NCO, more preferably 2.5% to 8.0%, or 3.0% to 7.2%, or 5.0% to 6.5%.

The chain extending substance may be selected from the group consisting of: 1, 3-butanediol, 1, 4-butanediol, ethylene glycol, diethylene glycol, triethylene glycol, tetraethylene glycol, propylene glycol, dipropylene glycol, tripropylene glycol, tetrapropylene glycol, 1, 3-propanediol, 1, 5-pentanediol, 1, 6-hexanediol, 1, 10-decanediol, neopentyl glycol, 1, 4-cyclohexanedimethanol, 1, 4-cyclohexanediol, glycerol, trimethylolpropane, dihydroxyethoxyhydroquinone, hydroquinone bis (2-hydroxyethyl) ether, 3-methyl-1, 5-pentanediol, p-xylylene glycol, 1, 4-bis- (. beta. -hydroxyethoxy) benzene, 1, 3-bis- (. beta. -hydroxyethoxy) benzene, cyclohexane 1, 4-dimethanol, octane-1, 8-diol and mixtures thereof.

Process for producing conventional thermosetting polyurethane

It is envisioned that in certain embodiments, at least one other layer of the golf ball may be comprised of a conventional thermoset or thermoplastic polyurethane, for example, to create a gradient of one or more properties, such as tensile strength at break, energy at break, and elongation at break, hardness, etc., between two given layers. In conventional thermoset polyurethane manufacturing processes, two basic techniques are used to prepare the polyurethane composition: a) one-shot techniques, and b) prepolymer techniques. In the one-shot technique, the isocyanate, polyol, and hydroxyl and/or amine terminated curing agent are reacted in one step. In contrast, prepolymer technology involves a first reaction between an isocyanate and a polyol compound to produce a polyurethane prepolymer, followed by a subsequent reaction between the prepolymer and a hydroxyl and/or amine terminated curing agent.

Some unreacted NCO groups are present in the polyurethane prepolymer due to the reaction between the isocyanate and the polyol compounds. The prepolymer typically has less than 14% unreacted NCO groups. As the weight percentage of unreacted isocyanate groups increases, the hardness of the composition generally increases.

In the one-shot process, the isocyanate compound is typically added to a reaction vessel, and then the curing agent mixture comprising the polyol and the curing agent is added to the reaction vessel. The components are mixed together such that the molar ratio of isocyanate compound to total polyol and curing agent compound is in the range of about 1.01:1.00 to about 1.10: 1.00. Preferably, the molar ratio is greater than 1.05: 1.00. For example, the molar ratio may be in the range of 1.07:1.00 to 1.10: 1.00. Generally, prepolymer technology is preferred because it provides better control of the chemical reaction. In the prepolymer method, the prepolymer is mixed with a curing agent such that the molar ratio of isocyanate groups to hydroxyl groups (and/or amine groups) is in the range of about 1.01:1.00 to about 1.10: 1.00. Preferably, the molar ratio is greater than 1.05: 1.00. For example, the molar ratio may be in the range of 1.07:1.00 to 1.10: 1.00.

The resulting polyurethane prepolymer contains urethane linkages (urethane linkages) having the general structure:

wherein x is the chain length, i.e., about 1 or greater, R and R₁Is a straight or branched hydrocarbon chain having from about 1 to about 20 carbon atoms.

Generally, polyurethanes are classified as thermoplastic or thermoset materials. Thermoplastic polyurethanes have some crosslinking, but they are predominantly through hydrogen bonding or other physical mechanisms. Thermoplastic polyurethanes are relatively flexible due to their low level of crosslinking. The crosslinks in the thermoplastic polyurethane can be reversibly broken by increasing the temperature during, for example, molding or extrusion. That is, the thermoplastic material softens when exposed to heat and returns to its original condition when cooled. On the other hand, thermoset polyurethanes become irreversibly cured upon curing. The cross-links irreversibly cure and are not destroyed when exposed to heat. Thus, thermoset polyurethanes, which typically have a high level of crosslinking, are relatively rigid.

In the conventional prepolymer process, the polyurethane prepolymer is chain extended by reaction with a single curative or a blend of curatives. Generally, the prepolymer can be reacted with a hydroxyl terminated curing agent, an amine terminated curing agent, or a mixture thereof. The curing agent extends the chain length of the prepolymer and increases its molecular weight.

When the polyurethane prepolymer is reacted with the hydroxyl terminated curing agent during the chain extension step, the resulting composition is a substantially pure polyurethane composition, as described above. On the other hand, when the polyurethane prepolymer is reacted with the amine-terminated curative during the chain extension step, any excess isocyanate groups in the prepolymer will react with the amine groups in the curative and produce urea linkages having the general structure:

wherein x is the chain length, i.e., about 1 or greater, R and R₁Is a straight or branched hydrocarbon chain having from about 1 to about 20 carbon atoms.

This chain extension step, which occurs when the polyurethane prepolymer is reacted with a hydroxyl terminated curative, an amine terminated curative or a mixture thereof, increases the molecular weight and extends the chain length of the prepolymer. When the polyurethane prepolymer is reacted with a hydroxyl terminated curing agent, a polyurethane composition having urethane linkages is produced. When the polyurethane prepolymer is reacted with an amine terminated curative, a polyurethane/urea hybrid composition having urethane and urea linkages results. The polyurethane/urea hybrid composition is different from the pure polyurethane composition. The concentration of urethane and urea linkages in the hybrid composition can vary. Typically, the hybrid composition may comprise a mixture of about 10 to 90 weight percent urethane and about 90 to 10 weight percent urea linkages. The resulting polyurethane composition or polyurethane/urea hybrid composition has elastomeric properties based on phase separation of soft and hard segments. The soft segments formed by the polyol reactant are generally flexible and mobile, while the hard segments formed by the isocyanate and chain extender are generally rigid and fixed.

When one layer of the golf ball further comprises a conventional polyurethane, non-limiting examples of suitable thermoplastic polyurethanes include those under the trade name250、255、260、270、950U、970U、1049、990DP7-1191、DP7-1202、990R、993、DP7-1049、3203、4203、4206、4210、4215 and3215 sold TPUs each commercially available from covesto LLC of Pittsburgh, Pa;50DT3、58212、55DT3、58887、EZ14-23A、ETE 50DT3, each commercially available from the Lubrizol Company of Cleveland, Ohio; andWY1149、1154D53、1180A、1190A、1195A、1185AW、1175AW, each commercially available from BASF;453, commercially available from Bayer, Pittsburgh, Pa., and E series TPUs, such as D60E 4024, commercially available from Huntsman Polyurethanes, Germany.

Thus, embodiments are contemplated wherein a golf ball of the invention comprises at least one layer of the thermoset polyurethane of the invention prepared by the method of the invention, as well as a conventional thermoset polyurethane prepared by the conventional method described above and/or a conventional thermoplastic polyurethane prepared by the conventional method described above. In such embodiments, a property gradient can be created between the layers of the thermoset polyurethane of the present invention and conventional polyurethane.

For example, by including a first layer comprising inventive prepolymer example 1 of tables I and II, formed by the process of the present invention and giving inventive material PU example 1 of table III, and a second layer of a golf ball comprising conventional prepolymer comparative example 1, formed by the conventional process described above and giving conventional material PU comparative example 1 of table III, it is possible to produce a gradient in tensile strength at break, a gradient in energy at break, and a gradient in% elongation at break in the golf ball of the present invention.

Examples of additional suitable materials for other golf ball layers

The at least one other layer can be comprised of, for example, partially neutralized ionomers and highly neutralized ionomers (HNPs), including ionomers formed from blends of two or more partially neutralized ionomers, blends of two or more highly neutralized ionomers, and blends of one or more partially neutralized ionomers with one or more highly neutralized ionomers.

As used herein, a highly neutralized polymer has greater than about 70% of the acid groups neutralized. In one embodiment, about 80% or more of the acid groups are neutralized. In another embodiment, about 90% or more of the acid groups are neutralized. In another embodiment, the HNPs are fully neutralized polymers, i.e., all acid groups (100%) in the polymer composition are neutralized.

As used herein, a partially neutralized polymer is understood to mean a polymer in which from about 10% to about 70% of the acid groups are neutralized.

At least one layer may be composed of a rubber composition comprising a rubber material such as polybutadiene, ethylene propylene rubber, ethylene propylene diene monomer, polyisoprene, styrene butadiene rubber, polycycloolefin, butyl rubber, halobutyl rubber or polystyrene elastomer.

Other suitable thermoplastic polymers that may be used to form the intermediate layer include, but are not limited to, the following polymers (including homopolymers, copolymers, and derivatives thereof): (a) polyesters, particularly polyesters modified with compatibilizing groups, such as sulfonates or phosphonates, including modified polyethylene terephthalate, modified polybutylene terephthalate, modified polypropylene terephthalate, modified polyvinyl naphthenate esters, and those disclosed in U.S. patents 6,353,050, 6,274,298, and 6,001,930, the entire disclosures of which are incorporated herein by reference, as well as blends of two or more thereof; (b) polyamides, polyamide-ethers and polyamide-esters, and those disclosed in U.S. patent nos. 6,187,864, 6,001,930, and 5,981,654, the entire disclosures of which are incorporated herein by reference, and blends of two or more thereof; (c) polyurethanes, polyureas, polyurethane-polyurea hybrids, and blends of two or more thereof; (d) fluoropolymers such as those disclosed in U.S. patent nos. 5,691,066, 6,747,110, and 7,009,002, the entire disclosures of which are incorporated herein by reference, and blends of two or more thereof; (e) polystyrenes, such as poly (styrene-maleic anhydride copolymer), acrylonitrile-butadiene-styrene, poly (styrene sulfonate), polyethylene styrene, and blends of two or more thereof; (f) polyvinyl chloride and grafted polyvinyl chloride, and blends of two or more thereof; (g) polycarbonates, blends of polycarbonate/acrylonitrile butadiene styrene, blends of polycarbonate/polyurethane, blends of polycarbonate/polyester, and blends of two or more thereof; (h) polyethers such as poly (arylene ether), polyphenylene ethers, block copolymers of alkenyl aromatic compounds with vinyl aromatic compounds and polyamic acid esters, and blends of two or more thereof; (i) polyimides, polyetherketones, polyamideimides, and blends of two or more thereof; (j) polycarbonate/polyester copolymers and blends.

It is also recognized that by crosslinking the polymer chains such that they form a network structure, the thermoplastic material can be "converted" into a thermoset material, and in accordance with the present invention, such crosslinked thermoplastic materials can be used to form the core layer and the intermediate layer. For example, thermoplastic polyolefins such as Linear Low Density Polyethylene (LLDPE), Low Density Polyethylene (LDPE), and High Density Polyethylene (HDPE) may be crosslinked to form bonds between polymer chains. Crosslinked thermoplastic materials generally have improved physical properties and strength over non-crosslinked thermoplastic materials, particularly at temperatures above the crystalline melting point. Preferably, the partially or fully neutralized ionomer as described above is covalently crosslinked to render it a thermoset composition (i.e., it contains at least some level of covalent, irreversible crosslinking). According to the invention, thermoplastic polyurethanes and polyureas can also be converted into thermosets.

The crosslinked thermoplastic material may be produced by exposing a thermoplastic material to: 1) high energy radiation treatment, such as electron beam or gamma radiation, as disclosed in U.S. patent 5,891,973, which is incorporated herein by reference; 2) low energy radiation, such as Ultraviolet (UV) or Infrared (IR) radiation; 3) solution treatments such as isocyanates or silanes; 4) introducing additional free radical initiator groups into the thermoplastic material prior to molding; and/or 5) chemical modifications, such as esterification or saponification, and the like.

Modification of the thermoplastic polymer structure can be induced by a number of methods, including exposure of the thermoplastic to high energy radiation or by chemical processes using peroxides. Radiation sources include, but are not limited to, gamma rays, electrons, neutrons, protons, X-rays, helium nuclei, and the like. Gamma radiation, usually using radioactive cobalt atoms, and allowing considerable depth of treatment if required. For core layers requiring lower penetration depths, electron beam accelerators or UV and IR light sources may be used. Useful methods of UV and IR irradiation are disclosed in U.S. patents 6,855,070 and 7,198,576, which are incorporated herein by reference. The thermoplastic layer may be irradiated at a dose greater than 0.05Mrd, or ranging from 1Mrd to 20Mrd, or ranging from 2Mrd to 15Mrd, or ranging from 4Mrd to 10 Mrd. In one embodiment, the layer may be irradiated at a dose from 5Mrd to 8Mrd, and in another embodiment, the layer may be irradiated at a dose from 0.05Mrd to 3Mrd, or from 0.05Mrd to 1.5 Mrd.

The solid core of the golf ball of the present invention may be manufactured using any suitable conventional technique, such as compression molding or injection molding. Typically, the core is formed by compression molding a blank of uncured or slightly cured rubber material into a spherical structure. Prior to forming the cover layer, the core structure may be surface treated to increase the adhesion between its outer surface and adjacent layers. Such surface treatment may include mechanical or chemical abrasion of the outer surface of the core. For example, the core may be subjected to corona discharge, plasma treatment, silane impregnation, or other treatment methods known to those skilled in the art. The cover layer is formed over the core or ball sub-assembly (core structure and any intermediate layers disposed around the core) using any suitable method described further below. Prior to forming the cover layer, the ball sub-assembly may be surface treated using the techniques described above to increase adhesion between its outer surface and the covering cover material.

Conventional compression and injection molding and other methods may be used to form the cover layer over the core or ball sub-assembly. Typically, compression molding typically involves first preparing a half (hemispherical) shell by injection molding the composition in an injection mold. This produces a semi-cured semi-rigid half shell (or cup). The half shells are then positioned in a compression mold around the core or ball subassembly. The half shells are fused together by the application of heat and pressure to form a cover layer over the core or subassembly. Compression molding may also be used to cure the cover composition after injection molding. For example, the heat curable composition may be injection molded around the core in an unheated mold. After the composition partially hardens, the balls are removed and placed in a compression mold. Heat and pressure are applied to the ball, which results in thermal curing of the cover layer.

Retractable Pin Injection Molding (RPIM) methods generally include the use of an upper mold cavity and a lower mold cavity that mate together. When the upper and lower mold cavities are joined together, they form a spherical internal cavity. The mold cavity used to form the cover skin has internal dimple cavity details. The cover material conforms to the interior geometry of the mold cavity to form a dimple pattern on the surface of the ball. The injection mold includes retractable support pins positioned throughout the mold cavity. The retractable support pins move into and out of the cavity. The support pins help to maintain the position of the ball core or ball subassembly as the molten composition flows through the mold gate. The molten composition flows into the cavity between the core and the mold cavity to surround the core and form the cover layer. Other methods may be used to manufacture the cover including, for example, Reaction Injection Molding (RIM), liquid injection molding, casting, spraying, powder coating, vacuum forming, flow coating, dipping, spin coating, and the like.

As noted above, an inner cover or intermediate layer, preferably formed from an ethylene acid copolymer ionomer composition, may be formed between the core or ball sub-assembly and the cover. The intermediate layer comprising the ionomer composition may be formed using conventional techniques, such as compression molding or injection molding. For example, the ionomer composition may be injection molded or placed in a compression mold to create the half shells. The shells are placed around the core in a compression mold and the shells are fused together to form the intermediate layer. Alternatively, the ionomer composition is injection molded directly onto the core using retractable pin injection molding.

After the golf balls have been removed from the mold, they may be subjected to finishing steps such as trimming, surface treatment, marking, and one or more coatings may be applied as desired by methods such as spraying, dipping, brushing, or rolling. The golf ball may then undergo a series of finishing steps.

For example, in a conventional white golf ball, a white cover layer may be surface treated using a suitable method, such as corona, plasma, or Ultraviolet (UV) light treatment. In another finishing process, the golf ball is coated with one or more paint coatings. For example, a white or clear primer may be first applied to the surface of the ball, and then the indicia may be applied to the primer followed by a clear polyurethane topcoat (top-coat). Indicia such as trademarks, symbols, logos, letters, etc. may be printed on the outer cover or primer or topcoat using pad printing, ink jet printing, thermal sublimation, or other suitable printing methods. Any surface coating may contain optical brighteners.

In general, the hardness, diameter, and thickness of the different ball layers may vary depending on the desired ball configuration. Thus, the golf balls of the present invention may have any known overall diameter and any known number of different layers and layer thicknesses to target desired playing characteristics.

The intermediate layer is sometimes considered to comprise any layer disposed between the inner core (or center) and the outer cover of the golf ball, and thus in some embodiments, the intermediate layer may comprise an outer core layer, an outer cover layer, or an inner cover layer. In this regard, golf balls of the present invention may include one or more intermediate layers. If desired, an intermediate layer may be used with the multilayer cover or multilayer core, or with both the multilayer cover and multilayer core.

The intermediate layer may be formed at least in part from one or more homo-or co-polymeric materials, such as ionomers, predominantly or completely non-ionomeric thermoplastic materials, vinyl resins, polyolefins, polyurethanes, polyureas, polyamides, acrylic resins and blends thereof, olefinic thermoplastic rubbers, block copolymers of styrene and butadiene, isoprene or ethylene-butylene rubbers, copoly (ether-amides), polyphenylene ether resins or blends thereof, and thermoplastic polyesters. However, embodiments are envisaged in which at least one intermediate layer is formed from a different material than is typically used for the core layer and/or the cap layer.

The thickness of the middle layer of a golf ball ranges widely due to the high potential for using the middle layer, i.e., as an outer core layer, inner cover layer, wrap layer, moisture/vapor barrier layer.

In view of the foregoing, embodiments are also contemplated in which one or more cap layers are formed of a material that is typically incorporated into a cap layer or an interlayer.

It is envisioned that the golf balls of the present invention may also incorporate conventional coatings for general bonding purposes.

It is envisioned that the layers of the golf ball of the present invention may be combined by any of casting, compression molding, injection molding, or thermoforming.

The resulting ball of the present invention has good impact durability and cut/shear resistance. The united states golf association ("USGA") has set a total weight limit for golf balls. In particular, USGA has established a maximum weight for a golf ball of 45.93g (1.62 ounces). There is no lower weight limit. In addition, the USGA requires that golf balls used in play have a diameter of at least 1.68 inches. There is no upper limit and therefore the overall diameter of many golf balls falls within the range of about 1.68 to about 1.80 inches. In accordance with the present invention, the weight, diameter and thickness of the core and cover layers may be adjusted as needed to meet USGA specifications for balls having a maximum weight of 1.62 ounces and a minimum diameter of at least 1.68 inches.

Preferably, the golf ball has a coefficient of restitution (CoR) of at least 0.750, more preferably at least 0.800 (measured according to the test method below). The core of a golf ball typically has a compressibility in the range of about 30 to about 130, and more preferably in the range of about 70 to about 110 (as measured according to the test method below). These characteristics enable players to generate greater ball speeds outside of the tee area and to achieve greater distances using a driver # 1 stick. At the same time, the relatively thin cover layer means that players will have a more comfortable and natural feel when hitting a ball with the club. The ball is easier to move and its flight path can be more easily controlled. This control allows the player to make better approach shots near the green. In addition, the cover of the present invention has good impact durability and mechanical strength.

The following test methods may be used to obtain certain properties associated with the inventive three-part thermoplastic blends of the present invention as well as other materials that may be incorporated into golf balls of the present invention.

Hardness.The center hardness of the core was obtained as follows. The core is gently pressed into a hemispherical fixture, the inner diameter of which is slightly smaller than the diameter of the core, to keep the core positioned in the hemispherical shape of the fixture while leaving the geometric center plane of the core exposed. The core is fixed in the holder by friction so that it does not move during the cutting and grinding steps, but the friction is not so great that it will cause a deformation of the natural shape of the core. The core is secured such that the parting line of the core is substantially parallel to the top of the clamp. The diameter of the core was measured at 90 degrees to this orientation prior to fixation. Measurements are also taken from the bottom of the fixture to the top of the core to provide a reference point for future calculations. Using band saws or the likeIts appropriate cutting tool makes a rough cut slightly above the exposed geometric center of the core, ensuring that the core does not move in the fixture during this step. The remainder of the core, still in the fixture, is secured to the base plate of the face grinder. Grinding the exposed "rough" surface to a smooth, flat surface, uncovering the geometric center of the core, which can be verified by measuring the height from the bottom of the fixture to the exposed surface of the core, ensuring that exactly half of the original height of the core as measured above has been removed (+ -0.004 inches). The core was left in the jig, the center of the core was found to have a central square and was carefully marked, and the hardness was measured at the center mark according to ASTM D-2240. Additional hardness measurements can then be made at any distance from the center of the core by drawing a line radially outward from the center mark and measuring the hardness at any given distance along that line, typically at 2mm increments from the center. The stiffness at a certain distance from the center should be measured along at least two, preferably four, radial arms spaced 180 ° or 90 ° apart, respectively, and then averaged. All hardness measurements taken on a plane passing through the geometric center are taken while the core is still in the fixture and without disturbing its orientation, so that the test surface is constantly parallel to the bottom of the fixture, and thus also to the properly aligned feet of the durometer.

The outer surface hardness of a golf ball layer is measured on the actual outer surface of the layer and is obtained from the average of a plurality of measurements taken from opposing hemispheres, taking care to avoid measurements on split lines or surface imperfections of the core, such as holes or protrusions. Hardness measurements were made according to ASTM D-2240 "indentation hardness of rubber and plastics by durometer". Due to the curved surface, care must be taken to ensure that the golf ball or golf ball subassembly is centered under the durometer indenter before a surface hardness reading is obtained. Hardness measurements were made using a calibrated digital durometer capable of reading to 0.1 hardness units. The digital durometer must be attached to the base of the robotic arm with its feet parallel to the base of the robotic arm. The weight on durometer and impact rate were in accordance with ASTM D-2240.

In certain embodiments, the point or points measured along the "positive" or "negative" gradient may be above or below the line fitted by the gradient and its outermost and innermost hardness values. In an alternative preferred embodiment, the hardest point along a particular steep "positive" or "negative" gradient may be higher than the value at the innermost (geometric center) or outer core layer (inner surface) of the inner core as long as the outermost point (i.e., the outer surface of the inner core) is either greater (for "positive") or lower (for "negative") than the innermost point (i.e., the geometric center of the inner core or the inner surface of the outer core layer), such that the "positive" and "negative" gradients remain intact.

As described above, the direction of the hardness gradient of a golf ball layer is defined by the difference in hardness measured at the outer and inner surfaces of the particular layer. The hardness of the inner core, the outer surface of the inner core in a single core ball, or the outer surface of the outer core layer is readily determined according to the test procedures provided above. The outer surface of the inner core layer (or other optional intermediate core layer) in a dual core ball is also readily determined according to the procedures set forth herein for measuring the hardness of the outer surface of a golf ball layer if the measurements are taken prior to surrounding the layer with an additional core layer. Once the additional core layer surrounds the layer of interest, it may be difficult to determine the hardness of the inner and outer surfaces of any inner or intermediate layers. Thus, for the purposes of the present invention, the test procedure described above for measuring a point located at a distance of 1mm from the interface is used when the hardness of the inner or outer surface of the core layer is required after the core layer is surrounded by another core layer.

Moreover, it should be understood that there is a fundamental difference between "material hardness" and "hardness measured directly on a golf ball". "for the purposes of this invention, material hardness is measured according to ASTM D2240, and generally includes measuring the hardness of a flat" plate "or" button "formed from the material. The direct measurement of surface hardness on a golf ball (or other spherical surface) typically results in different hardness values. The difference in the "surface hardness" and "material hardness" values is due to several factors, including, but not limited to, the ball configuration (i.e., core type, number of core and/or cover layers, etc.); ball (or sphere) diameter; and the material composition of adjacent layers. It should also be appreciated that the two measurement techniques are not linearly related, and therefore, one hardness value cannot be readily related to the other. Shore hardness (e.g., Shore C or Shore D or Shore A hardness) is measured according to test method ASTM D-2240.

Tensile strength,% elongation and energy at break.

As used herein, tensile strength,% elongation, and energy at break are each measured using ASTM D-412.

And (4) compressing.As disclosed in Jeff Dalton's Compression by Any Other Name, Science and gold IV, Proceedings of the World Scientific Congress of gold ("Eric Thain ed., Routeridge, 2002"), several different methods can be used to measure Compression, including Atti Compression, Riehle Compression, load/offset measurements at various fixed loads and offsets, and effective modulus. For purposes of the present invention, compression refers to the soft center deflection index ("SCDI"). SCDI is a programmed variation of a dynamic compression machine ("DCM") that allows the number of pounds required to deflect a sphere core 10% of its diameter to be determined. A DCM is a device that applies a load to a core or ball and measures the number of inches the core or ball deflects under the measured load. A raw load/deflection curve fitted to the Atti compression scale is generated, which results in a number representing the Atti compression. DCM is accomplished by a load cell attached to the bottom of a hydraulic cylinder that is pneumatically activated at a fixed rate (typically about 1.0ft/s) toward a fixed core. An LVDT is attached to the cylinder, which measures the distance the cylinder travels over the test time range. The software-based logarithmic algorithm ensures that measurements are not taken during the initial phase of the test until at least five consecutive increases in load are detected. SCDI is a slight variation of this setting. The hardware is the same, but the software and output have changed. For SCDI, the pound of force required to deflect the core by an amount of x inches is of interest. The deflection is 10% of the core diameter. The DCM is triggered, which deflects the core 10% of its diameter, reporting back the pounds of force required to deflect the core by that amount (as measured from the attached load cell). The values shown are individual numbers in pounds.

Coefficient of restitution ("CoR").CoR is determined according to known methods, where a golf ball or golf ball sub-assembly (e.g., golf ball core) is launched from an air cannon at two given speeds, and a speed of 125ft/s is used for the calculation. A ballistic light screen (light screen) was positioned between the air cannon and the steel plate at a fixed distance to measure the ball speed. As the ball travels towards the steel plate, it activates each light curtain and measures the time period for the ball at each light curtain. This provides an entry in-transit time period that is inversely proportional to the ball's entry velocity. The ball hits the steel plate and bounces back so it passes through the light curtain again. The time period of the ball at each light curtain was measured as the rebounded ball activated each light curtain. This provides a time-in-transit period of departure that is inversely proportional to the speed of departure of the ball. CoR is then calculated as the ratio of the ball's leaving in-transit time period to the ball's entering in-transit time period (CoR ═ V)_out/V_in＝T_in/T_out)。

The thermoset and thermoplastic layers herein may be treated in a manner that creates a positive or negative hardness gradient within and between the golf ball layers. In the golf ball layer of the present invention, wherein a thermoset rubber is used, a gradient generation method and/or a gradient generation rubber formulation may be used. Gradient generation methods and formulations are more fully disclosed in, for example, U.S. patent application serial No. 12/048,665 filed on 3/14, 2008; 11/829,461 filed on 27 th month 7 of 2007; 11/772,903 filed on 3/7/2007; 11/832,163 filed on 8/1 of 2007; 11/832,197 filed on 8/1 of 2007; the entire disclosure of each of these references is incorporated herein by reference.

It should be understood that the golf balls of the present invention, as described and illustrated herein, incorporate at least one layer of the three-part thermoplastic blend of the present invention, representing only some of the many embodiments of the present invention. Those skilled in the art will appreciate that various modifications and additions may be made to the golf ball without departing from the spirit and scope thereof. All of these embodiments are intended to be covered by the appended claims.

The golf balls of the present invention may also include indicia, which as used herein is considered to refer to any symbol, grouping of letters, design, etc., that may be added to the dimple surface of the golf ball.

The golf balls of the present invention generally have a dimple coverage of 60% or greater, preferably 65% or greater, and more preferably 75% or greater. It should be understood that any known dimple pattern may be used with any number of dimples having any shape or size. For example, the number of dimples may be 252 to 456 or 330 to 392 and may include any width, depth, and edge angle. The split line configuration of the pattern may be, for example, a straight line or a staggered wavy split line (SWPL).

In any of these embodiments, the single layer core may be replaced with two or more layers of core, wherein at least one of the core layers has a hardness gradient.

Other than in the operating examples, or unless otherwise expressly stated, all numerical ranges, amounts, values and percentages, such as those for amounts of material and others in the specification, may be read as if prefaced by the word "about", even though the term "about" may not expressly appear with the value, amount or range. Accordingly, unless indicated to the contrary, the numerical parameters set forth in the specification and attached claims are approximations that may vary depending upon the desired properties sought to be obtained by the present invention. At the very least, and not as an attempt to limit the application of the doctrine of equivalents to the scope of the claims, each numerical parameter should at least be construed in light of the number of reported significant digits and by applying ordinary rounding techniques.

Notwithstanding that the numerical ranges and parameters setting forth the broad scope of the invention are approximations, the numerical values set forth in the specific examples are reported as precisely as possible. Any numerical value, however, inherently contains certain errors necessarily resulting from the standard deviation found in their respective testing measurements. Further, when numerical ranges of different ranges are set forth herein, it is understood that any combination of these values, including the recited values, can be used.

Although the golf ball of the present invention has been described herein with reference to particular means and materials, it is to be understood that the invention is not limited to the particulars disclosed and extends to all equivalents within the scope of the claims.