Method of forming a golf ball core

• US 6,180,040 B1
• Filed: 09/02/1998
• Issued: 01/30/2001
• Est. Priority Date: 09/02/1998
• Status: Expired due to Term

• Current Assignee: Acushnet Company (FILA Holdings Corp.)
• Original Assignee: Acushnet Company (FILA Holdings Corp.)
• Inventors: Lutz, Mitchell E., Ladd, Derek A.
• Primary Examiner(s): Silbaugh, Jan H.
• Assistant Examiner(s): Lee, Edmund H.
• Application Number:
  US09/145,882
• Time in Patent Office: 881 Days
• Field of Search: 264/250, 264/266, 264/279.1, 264/320, 264/319, 264/347, 264/248, 264/255
• US Class Current: 264/248
• CPC Class Codes: B29C 2791/001 Shaping in several steps
• CPC Class Codes: B29C 43/146 for making multilayered articles
• CPC Class Codes: B29C 43/18 incorporating preformed parts or layers, e.g. compression moulding around inserts or for coating articles B29C43/206 takes precedence
• CPC Class Codes: B29C 63/22 using layers or sheathings having a shape adapted to the shape of the article B29C63/26 and B29C63/38 take precedence
• CPC Class Codes: B29K 2101/10 Thermosetting resins
• CPC Class Codes: B29K 2105/24 crosslinked or vulcanised
• CPC Class Codes: B29K 2105/243 Partially cured
• CPC Class Codes: B29L 2031/54 Balls
• CPC Class Codes: B29L 2031/546 Golf balls

Abstract

The invention includes methods of forming at least a portion of a golf ball core, and the golf balls prepared thereby, by mixing a resilient polymer component, a free radical initiator system, and a crosslinking agent to provide a first mixture, forming the first mixture into a plurality of shells having a desired shape, first heat curing the shells at a temperature to impart a rigidity sufficient to maintain the desired shape until the shells are assembled and subsequently heat cured, quenching the first heat curing by reducing the shell temperature to inhibit crosslinking while a sufficient amount of free radical initiator system is present to facilitate a second heat curing, providing a center, assembling at least two shells concentrically about the center to form a first mantle layer, wherein the first mantle layer and center together form the ball core, and second heat curing the core at a temperature and for a time sufficient to further crosslink the first mixture and to at least partially crosslink the shells, thereby forming a cured golf ball core.

Claims

1. A method of forming a golf ball core which comprises:

combining a resilient polymer component, a free radical initiator system, and a crosslinking agent to provide a first mixture;

forming the first mixture into a plurality of half-shells having a desired shape;

subjecting the half-shells to a first heat curing at a first temperature and time chosen to partially crosslink each half-shell so as to impart a rigidity sufficient to maintain the desired shape until the half-shells are assembled and subjected to a second heat curing, wherein a portion of the initiator system sufficient to initiate the second heat curing remains after the first heat curing;

providing a center;

assembling at least two half-shells concentrically about the center to form a first mantle layer, wherein the first mantle layer and center together form the ball core; and

subjecting the core to the second heat curing at a second temperature and for a time sufficient to further crosslink the half-shells, thereby forming a cured golf ball core.

2. The method of claim 1, wherein the desired shape comprises an ellipsoidal half-shell shape.

3. The method of claim 1, wherein the resilient polymer component is selected to have a high molecular weight average of between about 100,000 to 750,000.

4. The method of claim 1, which further comprises quenching the half-shells after the first heat curing by cooling the half-shells to a temperature below about 100°

F.

5. The method of claim 1, wherein the first mixture is formed into the shells by injection molding.

6. The method of claim 1, wherein the desired shape is provided by compression molding.

7. The method of claim 1, wherein the free radical initiator system comprises at least one low temperature initiator and at least one high temperature initiator, wherein the low temperature initiator is substantially consumed within about 15 minutes at a temperature from about 150°

F. to less than 300°

F. and the high temperature initiator is substantially consumed within 15 minutes at a temperature from 300°

F. to 400°

F.

8. The method of claim 7, wherein the low temperature initiator and the high temperature initiator are each selected to be an organic peroxide.

9. The method of claim 1, wherein the first curing temperature is from about 150°

F. to 300°

F. and the second curing temperature is from about 300°

F. to 400°

F.

10. The method of claim 1, wherein the first curing is conducted over about 30 seconds to 15 minutes and the second curing is conducted over about 5 minutes to 25 minutes.

11. The method of claim 1, wherein the center comprises at least one of a wound center, a solid center, or a liquid center.

12. The method of claim 1, which further comprises forming at least one additional layer about the center prior to assembling the half-shells concentrically about the center, after assembling the half-shells concentrically about the center, or after the second heat curing of the core.

13. The method of claim 12, wherein the at least one additional layer is formed after the second heat curing of the core to provide a cover disposed concentrically about the golf ball core, thereby forming a golf ball.

14. The method of claim 8, wherein the low temperature peroxide component is selected from the group consisting of decanoyl peroxide, lauroyl peroxide, succinic acid peroxide, benzoyl peroxide, di(n-propyl)peroxydicarbonate, di(sec-butyl)peroxydicarbonate, di(2-ethylhexyl)peroxydicarbonate, 1,1-dimethyl-3-hydroxybutyl peroxyneodecanoate, α

-cumyl peroxyneodecanoate, 1,1-dimethyl-3-hydroxy-butyl-peroxyneoheptanoate, α

-cumyl peroxyneoheptanoate, t-amyl peroxyneodecanoate, t-butyl peroxyneodecanoate, t-amyl peroxypivalate, t-butyl peroxypivalate, 2,5-dimethyl 2,5-di(2-ethylhexnoylperoxy)hexane, t-amyl peroxy-2-ethyl-hexanoate, t-butyl peroxy-2-ethylhexanoate, t-butyl peroxyacetate, t-amyl peroxyacetate, t-butyl perbenzoate, t-amyl perbenzoate, OO-t-amyt-O (2-ethylhexyl) monoperoxycarbonate, di-t-butyl diperoxyphthalate, OO-t-butyl-O-isopropyl monoperoxycarbonate, 2,5-dimethyl-2,5-di(benzoylperoxy)hexane, OO-t-butyl-1-(2-ethylhexyl)monoperoxycarbonate, 1,1-di(t-butylperoxy)-3,3,5-trimethylcyclohexane, 1,1-di-(t-butylperoxy)-cyclohexane, 1,1-di-(t-amylperoxy)-cyclohexane, ethyl-3,3-di-(t-butylperoxy)-butyrate, ethyl-3,3-di-(t-amylperoxy)-butyrate, and mixtures thereof, and the high temperature peroxide component is selected from the group consisting of dicumyl peroxide, 2,5-dimethyl-2,5-di-(t-butylperoxy)hexane, α

, α

′

-bis(t-butylperoxy)diisopropyl-benzene, di-t-butyl peroxide, di-t-amyl peroxide, 2,5-dimethyl-2,5-di-(t-butylperoxy)hexyne-3, cumene hydroperoxide, t-butyl hydroperoxide, t-amyl hydroperoxide, and mixtures thereof.

15. The method of claim 1, wherein the crosslinking agent is selected to be a metallic salt selected from the group consisting of an unsaturated fatty acid, an α

,β

-monoethylenic unsaturated carboxylic acid, and mixtures thereof.

16. The method of claim 1, wherein the resilient polymer component is selected to be present in an amount from about 35 to 80 weight percent of the first mixture.

17. The method of claim 1, which further comprises providing a filler comprising at least one of a coloring agent, zinc oxide, tin oxide, barium sulfate, zinc sulfate, calcium carbonate, barium carbonate, clay, tungsten, tungsten carbide, silica, or carbon black to the first mixture, wherein the filler is present in an amount from about 0.5 to 50 weight percent of the composition.

18. The method of claim 15, further comprising a crosslinking coagent of an acrylate functional moiety.

19. The method of claim 18, wherein the crosslinking coagent is selected from the group consisting of ethylene glycol dimethacrylate, 1,3-butylene glycol dimethacrylate, trimethylolpropane trimethacrylate, and a mixture thereof.

20. A method of forming a golf ball core which comprises:

combining a 1,4-cis-polybutadiene, a low temperature peroxide, a high temperature peroxide, and a crosslinking agent to provide a first mixture;

forming the first mixture into a plurality of semi-ellipsoidal half-shells;

subjecting the half-shells to a first heat curing at a first temperature between about 200°

F. to 300°

F. for about 30 seconds to 15 minutes to impart a rigidity sufficient to maintain the semi-ellipsoidal shape until the half-shells are assembled and subjected to a second heat curing, wherein at least about 50 weight percent of the high temperature peroxide remains after the first heat curing to initiate the second heat curing;

providing a center;

assembling at least two semi-ellipsoidal half-shells concentrically about the center to form a first mantle layer, wherein the first mantle layer and center together form the ball core; and

subjecting the core to the second heat curing at a second temperature between about 310°

F. to about 390°

F. for about 5 to 25 minutes to further crosslink the shells, thereby forming a cured golf ball core.

21. A method of forming a golf ball core which comprises:

combining about 35 to 80 weight percent 1,4-cis-polybutadiene, an amount of low temperature peroxide that reacts at a temperature of between about 210°

F. to 290°

F., a high temperature peroxide that reacts at a temperature of between about 320°

F. to 380°

F. and is present in an amount greater than the low temperature peroxide, and a crosslinking agent to provide a first mixture;

forming the first mixture into a plurality of semi-ellipsoidal half-shells;

subjecting the half-shells to a first heat curing at a first temperature between about 210°

F. to 290°

F. for about 1 to 15 minutes to impart a rigidity sufficient to maintain the semi-ellipsoidal shape until the half-shells are assembled and subjected to a second heat curing, wherein at least about 50 weight percent of the high temperature peroxide remains after the first heat curing to initiate the second heat curing;

providing a center;

assembling at least two semi-ellipsoidal half-shells concentrically about the center to form a first mantle layer, wherein the first mantle layer and center together form the ball core; and

subjecting the core to the second heat curing at a second temperature between about 320°

F. to 380°

F. for about 5 to 25 minutes to further crosslink the shells, thereby forming a cured golf ball core.