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Golf Ball Layers Formed of Polyurethane-Based and Polyurea-Based Compositions Incorporating Block Copolymers

a technology of polyurea-based compositions and golf balls, which is applied in the field of golf ball layers formed of polyurea-based compositions incorporating block copolymers, can solve the problems of poor spin and feel, easy damage of balata covered balls, and lack of durability required by the average golfer

Inactive Publication Date: 2009-05-28
ACUSHNET CO
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0014]The present invention is generally directed to golf equipment having at least a portion formed of a polyurea composition. In one embodiment, the present invention is directed to one-piece golf balls including polyurea. In another embodiment, the compositions of the invention are used in two-piece and multi-component,

Problems solved by technology

However, balata covered balls are easily damaged, and thus lack the durability required by the average golfer.
However, while SURLYN® covered golf balls, as described in the preceding patents, possess virtually cut-proof covers, the spin and feel are inferior compared to balata covered balls.
However, golf ball covers made from polyurethane have not, to date, fully matched SURLYN® golf balls with respect to resilience or the rebound of the golf ball cover, which is a function of the initial velocity of a golf ball after impact with a golf club.
Furthermore, because the polyurethanes used to make the covers of such golf balls generally contain an aromatic component, e.g., aromatic diisocyanate, polyol, or polyamine, they are susceptible to discoloration upon exposure to light, particularly ultraviolet (UV) light.
The application of a uniform white pigmented coat to the dimpled surface of the golf ball is a difficult process that adds time and costs to the manufacture of a golf ball.
In addition, while certain polyols provide more stability to the polyurethane polymer in terms of moisture resistance, polyurethanes remain highly susceptible to changes in their physical properties due to absorption of moisture.
Once these two ingredients are combined, the polyurea is formed, and thus the ability to vary the physical properties of the composition is limited.

Method used

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  • Golf Ball Layers Formed of Polyurethane-Based and Polyurea-Based Compositions Incorporating Block Copolymers
  • Golf Ball Layers Formed of Polyurethane-Based and Polyurea-Based Compositions Incorporating Block Copolymers
  • Golf Ball Layers Formed of Polyurethane-Based and Polyurea-Based Compositions Incorporating Block Copolymers

Examples

Experimental program
Comparison scheme
Effect test

example 1

Saturated Polyurethane Golf Ball Cover

[0306]Table 3 illustrates the components used to make a saturated polyurethane golf ball cover composition.

TABLE 3COMPOSITIONChemicalsWeight (g)H12MDI Prepolymer*458.731,4-Butanediol42.75HCC-19584 Color Dispersion**17.55*Prepolymer is the reaction product of 4,4′-dicyclohexylmethane diisocyanate and polytetramethylene ether glycol.**HCC-19584 is a white-blue color dispersion manufactured by the PolyOne Corporation (formerly the Harwick Chemical Corporation)

[0307]A golf ball was made having the cover formulated from the composition above following the teachings of U.S. Pat. No. 5,733,428. The physical properties and the ball performance results are listed in Table 4.

TABLE 4PHYSICAL PROPERTIESPhysical PropertiesPresent InventionCover Hardness54Weight (g)45.58Compression89Shear ResistanceGoodColor StabilityComparable toSURLYN ®

The molded balls from the above composition listed in Table 4 were further subject to a QUV test as described below:

Method:...

example 2

H12 MDI Polyether Urea Cured with Diol

[0315]A golf ball was made having the cover formulated from a composition including a prepolymer formed of H12MDI and polyoxyalkylene, having a molecular weight of about 2000, cured with 1,4-butanediol. The physical properties and the ball performance results are listed in Table 8. A golf ball similar to Example 1, a light stable, aliphatic polyurethane, was used for comparison purposes.

TABLE 8PHYSICAL PROPERTIESBall TypesAliphatic PolyurethaneBall PropertiesControlInventionNameplate Average1.6861.684Equator Average1.6841.683Weight Average, oz1.5991.595Compression Average8686COR @ 125 ft / sec0.8070.805Cold Crack Test, 5° F.no failureno failureLight Stability (5 Days QUV Test)ΔYI3.20.8Δb*1.70.4Live Golfer Shear Test*Damage Rank32Appearance Rank32*Rating of Shear Test: Based on a scale of 1-9, 1 is the best, 9 is the worst.

example 3

H12MDI Polyether Urea Cured with a Diamine

[0316]A golf ball was made having the cover formulated from a composition including a prepolymer formed of H12MDI and polyoxyalkylene, having a molecular weight of about 2000, cured with 4,4′-bis-(sec-butylamino)-dicyclohexylmethane (Clearlink 1000). The physical properties and the ball performance results are listed in Table 9. A golf ball similar to Example 1, a light stable, aliphatic polyurethane, was used for comparison purposes.

TABLE 9PHYSICAL PROPERTIESBall TypesLight StableBall PropertiesPolyurethane ControlInventionNameplate Average1.6831.686Equator Average1.6811.684Weight Average, oz1.5971.600Compression Average8992COR @ 125 ft / sec0.8070.815Cold Crack Test, 5° F.no failureno failureLight Stability (5 Days QUV Test)ΔYI4.30.6Δb*2.40.3Live Golfer Shear Test*Damage Rank31Appearance Rank31*Rating of Shear Test: Based on a scale of 1-9, 1 is the best, 9 is the worst.

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Abstract

A golf ball including a core and a cover, wherein cover is formed from a composition comprising the reaction product of a prepolymer including a soft-segment comprising an amine-terminated polyether and a hard segment including a uretdione of hexamethylene diisocyanate; and an amine-terminated curing agent; wherein the amine-terminated polyether has the structure:where x and z have a combined value of 3.6-8 and y is 9-50, R is an alkyl group having 1-20 carbons, a phenyl group, a cyclic group, or mixtures thereof, R1 is —(CH2)a—, where a is 1-10, a phenylene group, a cyclic group, or a mixture thereof, and R3 is hydrogen, a methyl group, or a mixture thereof.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS[0001]This application is a continuation of co-pending U.S. patent application Ser. No. 11 / 785,496, filed Apr. 18, 2007, which is a continuation of U.S. patent application Ser. No. 10 / 900,468, filed Jul. 28, 2004, now U.S. Pat. No. 7,211,624, which is a continuation-in-part of U.S. patent application Ser. No. 10 / 409,092, filed Apr. 9, 2003, now U.S. Pat. No. 6,964,621, which is a continuation-in-part of U.S. patent application Ser. No. 10 / 066,637, filed Feb. 6, 2002, now U.S. Pat. No. 6,582,326, which is a continuation of U.S. patent application Ser. No. 09 / 453,701, filed Dec. 3, 1999, now U.S. Pat. No. 6,435,986; and also a continuation-in-part of U.S. patent application Ser. No. 10 / 228,311, filed Aug. 27, 2002, now U.S. Pat. No. 6,835,794, which is a continuation-in-part of U.S. patent application Ser. No. 09 / 466,434, filed Dec. 17, 1999, now U.S. Pat. No. 6,476,176, and a continuation-in-part of U.S. patent application Ser. No. 09 / 951,963, f...

Claims

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Application Information

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IPC IPC(8): A63B37/02A63B37/12A63B37/04A63B37/00A63B37/06A63B37/08A63B45/00C08L75/02C08L75/04
CPCA63B37/0003A63B37/0083A63B2209/00A63B2225/60A63B37/0024A63B37/0027A63B37/0039A63B37/0045A63B37/0047A63B37/0049A63B37/0052A63B37/0056A63B37/0074A63B37/0075A63B37/0076A63B37/008A63B37/12
Inventor WU, SHENSHENRAJAGAPALAN, MURALIHARRIS, KEVIN M.
Owner ACUSHNET CO