IP Library Granted Patent US 9,211,444
Granted Patent B2
US 9,211,444 · App. 13/941,749 · Granted Dec 15, 2015

Methods for making polyurea polymer and golf balls prepared therefrom

Inventors: Michael Michalewich (Mansfield, MA); Brian Comeau (Berkley, MA); David A. Bulpett (Boston, MA); Shawn Ricci (New Bedford, MA)
Assignee: Acushnet Company
A63B37/0027A63B37/0075C08G18/10C08G18/721C08G18/722C08G18/792C08L75/02
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Quick Facts
Patent No.
US 9,211,444
App. No.
13/941,749
Filed
Jul 15, 2013
Granted
Dec 15, 2015
Kind
B2
Art Unit
1765
USPC
528/61
Abstract

Methods for making golf balls having a cover made from a polyurea composition are provided. The golf balls include a rubber core and intermediate layer made from an olefin-based ionomer composition. The methods for making the polyurea composition involve preparing an amine-terminated first polymer by reacting isocyanate compound A with a stoichiometric excess of polyamine. The first prepolymer is reacted with a stoichiometric excess of isocyanate compound B to form an isocyanate-terminated second prepolymer. The second prepolymer is then reacted with a chain extender.

Claims (14)

1. A method of forming a golf ball comprising a core formed from a rubber material, an intermediate layer formed from an olefin-based ionomer, and cover formed from a polyurea composition, the intermediate layer being disposed between the core and cover, and the polyurea composition being prepared by a reaction comprising the steps of:

i) forming an amine-terminated first prepolymer by reacting isocyanate compound A with a stoichiometric excess of polyamine compound;

ii) forming an isocyanate-terminated second prepolymer by reacting the first prepolymer with a stoichiometric excess of isocyanate compound B; and

iii) reacting the second prepolymer with an amine-terminated chain extender, wherein isocyanate compound A is 4,4′-diisocyanatodicyclohexylmethane diisocyanate (H 12 MDI) and isocyanate compound B is 1,6-hexamethylene diisocyanate (HDI) oligomer.

2. The method of claim 1 , wherein the rubber material is selected from the group consisting of polybutadiene rubber, polyisoprene rubber, natural rubber, ethylene-propylene rubber, ethylene-propylene diene rubber, styrene-butadiene rubber, and blends thereof.

3. The method of claim 2 , wherein the rubber material is polybutadiene rubber.

4. The method of claim 1 , wherein the rubber material is a blend of polybutadiene rubber and an elastomer selected from the group consisting of polyisoprene rubber, natural rubber, ethylene propylene rubber, ethylene propylene diene rubber, styrene-butadiene rubber, polystyrene elastomers, polyethylene elastomers, polyurethane elastomers, polyurea elastomers, acrylate rubbers, polyoctenamers, metallocene-catalyzed elastomers, and plastomers.

5. The method of claim 1 , wherein the olefin-based ionomer is an ethylene acid copolymer, the acid being selected from methacrylic acid, acrylic acid, maleic acid, crotonic acid, fumaric acid, and itaconic acid.

6. The method of claim 5 , wherein 10 to 80% of the acid groups in the olefin-based ionomer are neutralized.

7. The method of claim 1 , wherein 80 to 100% of the acid groups in the olefin-based ionomer are neutralized.

8. A method of forming a golf ball comprising a core formed from a rubber material, an intermediate layer formed from an olefin-based ionomer, and cover formed from a polyurea composition, the intermediate layer being disposed between the core and cover, and the polyurea composition being prepared by a reaction comprising the steps of:

i) forming an amine-terminated first prepolymer by reacting isocyanate compound A with a stoichiometric excess of polyamine compound;

ii) forming an isocyanate-terminated second prepolymer by reacting the first prepolymer with a stoichiometric excess of isocyanate compound B; and

iii) reacting the second prepolymer with an amine-terminated chain extender, wherein isocyanate compound A is 2,4-toluene diisocyanate (TDI) and isocyanate compound B is 4,4′-diphenylmethane diisocyanate (MDI).

Assignments (6)
SECURITY INTEREST Recorded Aug 3, 2022
From: ACUSHNET COMPANY
To: JPMORGAN CHASE BANK, N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 061099/0236 →
ASSIGNMENT OF SECURITY INTEREST IN PATENTS (ASSIGNS 039506-0030) Recorded Aug 3, 2022
From: WELLS FARGO BANK, NATIONAL ASSOCIATION, AS RESIGNING ADMINISTRATIVE AGENT
To: JPMORGAN CHASE BANK, N.A., AS SUCCESSOR ADMINISTRATIVE AGENT
Reel/Frame 061521/0414 →
RELEASE OF SECURITY INTEREST IN PATENTS PREVIOUSLY RECORDED AT REEL/FRAME (032019/0075) Recorded Sep 7, 2016
From: KOREA DEVELOPMENT BANK, NEW YORK BRANCH
To: ACUSHNET COMPANY
Reel/Frame 039939/0405 →
SECURITY INTEREST Recorded Jul 28, 2016
From: ACUSHNET COMPANY
To: WELLS FARGO BANK, NATIONAL ASSOCIATION, AS ADMINISTRATIVE AGENT
Reel/Frame 039506/0030 →
SECURITY AGREEMENT Recorded Jan 14, 2014
From: ACUSHNET COMPANY
To: KOREA DEVELOPMENT BANK, NEW YORK BRANCH
Reel/Frame 032019/0075 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 15, 2013
From: MICHALEWICH, MICHAEL; COMEAU, BRIAN; BULPETT, DAVID A.; RICCI, SHAWN
To: ACUSHNET COMPANY
Reel/Frame 030795/0957 →
Continuity (2)
Continuation 12975491 · Dec 22, 2010
Related Publication 20130303697A1 · Nov 14, 2013