U.S. patent application number 11/936827 was filed with the patent office on 2008-03-13 for golf ball with vapor barrier layer.
Invention is credited to Michael D. Jordan.
Application Number | 20080064528 11/936827 |
Document ID | / |
Family ID | 25538358 |
Filed Date | 2008-03-13 |
United States Patent
Application |
20080064528 |
Kind Code |
A1 |
Jordan; Michael D. |
March 13, 2008 |
GOLF BALL WITH VAPOR BARRIER LAYER
Abstract
A multi-layer golf ball comprising a core, a water vapor barrier
layer and a cover is provided. The core may have any construction
and may have multiple layers. The core may also have a solid or
liquid center or wound layers, and may be constructed from a
polybutadiene with mid to high Mooney viscosity. The water vapor
barrier layer preferably comprises a copolymer of ethylene and
methacrylic acid. The water vapor barrier layer may also include
either an acid terpolymer, such as a terpolymer of ethylene, methyl
acrylate and acrylic acid, or a copolymer of ethylene and acrylic
acid, or both. Preferably, the water vapor barrier layer has an
acid content of about 3% by weight to about 25% by weight. In
accordance to another aspect of the invention, the water vapor
barrier layer has a high flow melt index, such that a thin layer
from about 0.030 inch to about 0.005 inch can be achieved. The
outer cover can be made from any suitable material. Preferably, the
outer cover is made from a thermoset polyurethane.
Inventors: |
Jordan; Michael D.; (East
Greenwich, RI) |
Correspondence
Address: |
ACUSHNET COMPANY
333 BRIDGE STREET
P. O. BOX 965
FAIRHAVEN
MA
02719
US
|
Family ID: |
25538358 |
Appl. No.: |
11/936827 |
Filed: |
November 8, 2007 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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10077081 |
Feb 15, 2002 |
7306528 |
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11936827 |
Nov 8, 2007 |
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09992448 |
Nov 16, 2001 |
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10077081 |
Feb 15, 2002 |
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Current U.S.
Class: |
473/374 |
Current CPC
Class: |
A63B 37/0045 20130101;
A63B 37/0033 20130101; A63B 37/0054 20130101; A63B 37/0065
20130101; A63B 37/0046 20130101; A63B 37/0024 20130101; A63B
37/0003 20130101; A63B 37/0093 20130101; A63B 37/0034 20130101;
A63B 37/0051 20130101; A63B 37/0036 20130101 |
Class at
Publication: |
473/374 |
International
Class: |
A63B 37/00 20060101
A63B037/00 |
Claims
1. A golf ball comprising a core, a moisture vapor barrier layer,
and a cover, wherein the moisture vapor barrier layer has a
moisture vapor transmission rate that is lower than that of the
cover, and comprises: a copolymer of ethylene and methacrylic acid;
and a terpolymer of ethylene, a softening acrylate class ester, and
a carboxylic acid.
2. The golf ball of claim 1, wherein the terpolymer is a terpolymer
of ethylene, methyl acrylate and acrylic acid.
3. The golf ball of claim 1, wherein at least one of the copolymer
and the terpolymer is non-ionomeric.
4. The golf ball of claim 1, wherein the terpolymer is a terpolymer
of ethylene, an ester being methyl acrylate, n-butyl acrylate or
iso-butyl acrylate, and an acid being acrylic acid or methacrylic
acid.
5. The golf ball of claim 1, wherein the moisture vapor barrier
layer further comprises a copolymer of ethylene and acrylic
acid.
6. The golf ball of claim 1, wherein the water vapor barrier layer
has a Shore D hardness of about 23 to about 63.
7. The golf ball of claim 1, wherein the water vapor barrier layer
has a moisture vapor transmission rate of less than about 0.95
gramsmm/m.sup.2day.
8. The golf ball of claim 1, wherein the water vapor barrier layer
further comprises a second non-ionomeric material having a melt
flow index of greater than 14 grams/10 minutes.
Description
STATEMENT OF RELATED PATENT APPLICATION
[0001] This non-provisional utility patent application is a
divisional of co-pending U.S. patent application Ser. No.
10/077,081, filed on Feb. 15, 2002, which is a continuation-in-part
of a co-pending patent application entitled "Low Spin Soft
Compression Performance Golf Ball" filed on Nov. 16, 2001 bearing
Ser. No. 09/992,448. The parent applications are hereby
incorporated by reference in their entirety.
FIELD OF THE INVENTION
[0002] The present invention relates to a novel structure for a
golf ball, and more particularly to a golf ball with a thin
moisture vapor barrier layer.
BACKGROUND OF THE INVENTION
[0003] Solid core golf balls are well known in the art. Typically,
the core is made from polybutadiene rubber material, which provides
the primary source of resiliency for the golf ball. U.S. Pat. Nos.
3,241,834 and 3,313,545 disclose the early work in polybutadiene
chemistry. It is also known in the art that increasing the
cross-link density of polybutadiene can increase the resiliency of
the core. The core is typically protected by a cover from repeated
impacts from golf clubs. The golf ball may comprise additional
layers, which can be an outer core or an inner cover layer. One or
more of these additional layers may be a wound layer of stretched
elastic windings to increase the ball's resiliency.
[0004] A known drawback of polybutadiene cores cross-linked with
peroxide and/or zinc diacrylate is that this material is adversely
affected by moisture. Water moisture vapor reduces the resiliency
of the cores and degrades its properties. A polybutadiene core will
absorb water and loose its resilience. Thus, these cores must be
covered quickly to maintain optimum ball properties. The cover is
typically made from ionomer resins, balata, and urethane, among
other materials. The ionomer covers, particularly the harder
ionomers, offer some protection against the penetration of water
vapor. However, it is more difficult to control or impart spin to
balls with hard covers. Conventional urethane covers, on the other
hand, while providing better ball control, offer less resistance to
water vapor than ionomer covers.
[0005] Prolonged exposure to high humidity and elevated temperature
may be sufficient to allow water vapor to invade the cores of some
commercially available golf balls. For example at 110.degree. F.
and 90% humidity for a sixty day period, significant amounts of
moisture enter the cores and reduce the initial velocity of the
balls by 1.8 ft/s to 4.0 ft/s or greater. The change in compression
may vary from 5 PGA to about 10 PGA or greater. The absorbed water
vapor also reduces the coefficient of restitution (COR) of the
ball.
[0006] Several prior patents have addressed the water vapor
absorption problem. U.S. Pat. No. 5,820,488 discloses a golf ball
with a solid inner core, an outer core and a water vapor barrier
layer disposed therebetween. The water vapor barrier layer
preferably has a water vapor transmission rate lower than that of
the cover layer. The water vapor barrier layer can be a
polyvinylidene chloride (PVDC) layer. It can also be formed by an
in situ reaction between a barrier-forming material and the outer
surface of the core. Alternatively, the water vapor barrier layer
can be a vermiculite layer. U.S. Pat. Nos. 5,885,172 and 6,132,324
disclose, among other things, a golf ball with a polybutadiene or
wound core with an ionomer resin inner cover and a relatively soft
outer cover. The hard ionomer inner cover offers some resistance to
water vapor penetration and the soft outer cover provides the
desirable ball control. Additionally, U.S. Pat. No. 5,875,891
discloses an impermeable packaging for golf balls. The impermeable
packaging acts as a moisture barrier limiting moisture absorption
by golf balls during storage but not during use.
[0007] It is also desirable to minimize the thickness of the water
barrier layer such that other properties of the ball are
unaffected. None of these references, however, discloses an
efficient way to make a thin layer of water vapor barrier layer,
that otherwise would not alter the performance of the ball.
[0008] Hence, there remains a need for other golf balls with an
improved water vapor barrier layer and improved methods for
applying a water vapor barrier layer on to the core of the golf
ball.
SUMMARY OF THE INVENTION
[0009] The present invention is directed to a golf ball comprising
a core, a cover and a thin film of moisture vapor barrier with a
moisture vapor transmission rate preferably lower than that of the
cover to decrease the amount of moisture penetrating into the core
of the golf ball. The moisture vapor barrier layer preferably
comprises a copolymer of ethylene and methacrylic acid. The
moisture vapor barrier layer may also comprise a terpolymer of
ethylene, a softening acrylate class ester such as methyl acrylate,
n-butyl-acrylate or iso-butyl-acrylate, and a carboxylic acid such
as acrylic acid or methacrylic acid. The moisture vapor barrier
layer may further comprise a copolymer of ethylene and acrylic
acid. Alternatively, the moisture vapor barrier layer may comprise
all three materials. In accordance to another aspect of the
invention, the preferred copolymer of ethylene and methacrylic acid
is polyethylene methacrylic acid resin.
[0010] In accordance to another aspect of the invention, the
preferred moisture vapor barrier materials have about 3% to about
25% of acid by weight, more preferably in the range of about 4% to
15%, and most preferably about 7% to about 11% of acid by weight.
The preferred copolymers also have high melt flow index. High melt
flow index of the preferred materials helps to reduce the thickness
of the moisture vapor barrier layer. A readily apparent advantage
of having a thin barrier layer is that it does not significantly
alter the predetermined and desired properties of the designed golf
ball. Preferably, the moisture vapor barrier has a thickness of
about 0.020 inch to about 0.005 inch. Preferably, the moisture
vapor barrier layer is made from two molded half shells that are
compression-molded on to the core.
[0011] In accordance to another aspect of the invention, the
moisture vapor barrier can be an intermediate layer, an inner cover
layer, an outer core layer, a core coating or an outer cover
coating. The present invention is also directed to a golf ball
having a relatively large solid polybutadiene core, a thin moisture
vapor barrier layer with a thermoset urethane cover. Alternatively,
the water vapor barrier layer of the present invention can be used
with any known core structures and covers.
BRIEF DESCRIPTION OF THE DRAWINGS
[0012] In the accompanying drawings, which form a part of the
specification and are to be read in conjunction therewith and in
which like reference numerals are used to indicate like parts in
the various views:
[0013] FIG. 1 is a front view of a dimpled golf ball in accordance
to the present invention;
[0014] FIG. 2 is a cross-sectional view of the golf ball in FIG. 1
showing a solid core surrounded by a thin moisture vapor barrier
layer and a cover; and
[0015] FIG. 3 is a cross-sectional view of another golf ball in
accordance to the present invention showing a solid core with
multiple wound layers surrounded by a thin moisture vapor barrier
layer.
DETAILED DESCRIPTION OF THE INVENTION
[0016] As shown generally in FIGS. 1 and 2, where like numbers
designate like parts, reference number 10 broadly designates a golf
ball in accordance to the present invention. Golf ball 10
preferably has a solid core 12, an intermediate layer 14 and a
cover 16.
[0017] Solid core 12 may comprise a single spherical element, or it
may comprise a core spherical element with one or more intermediate
layers surrounding the spherical element as shown in FIG. 3. Solid
core 12 can be made from any suitable core materials including
thermoset plastics, such as natural rubber, polybutadiene (PBD),
polyisoprene, styrene-butadiene or styrene-propylene-diene rubber,
and thermoplastics such as ionomer resins, polyamides, polyesters,
or a thermoplastic elastomer. Suitable thermoplastic elastomers
include Pebax.RTM., Hytrel.RTM., thermoplastic urethane, and
Kraton.RTM., which are commercially available from Elf-Atochem,
E.I. Du Pont de Nemours and Company, various manufacturers, and
Shell Chemical Company, respectively. The core materials can also
be formed from a castable material. Suitable castable materials
include those comprising a urethane, polyurea, epoxy, silicone,
IPN's, etc.
[0018] Additionally, suitable core materials may also include a
reaction injection molded polyurethane or polyurea, including those
versions referred to as nucleated, where a gas, typically nitrogen,
is essentially whipped into at least one component of the
polyurethane, typically, the pre-polymer, prior to component
injection into a closed mold where essentially full reaction takes
place resulting in a cured polymer having reduced specific gravity.
These materials are referred to as reaction injection molded (RIM)
materials. Alternatively, core 12 may include a liquid center, such
as center 12a shown in FIG. 3, and may have one or more would
layers, such as intermediate layers 12b and 12c.
[0019] Preferably, core 12 is made from a polybutadiene with a mid
to high range Mooney viscosity, which provides a soft but high
velocity core. The core may be blended with an organic sulfur
plasticizer such as pentachlorolthiophenol or a Zinc salt of
pentachlorolthiophenol to further increase the softness and
resiliency of the core.
[0020] The core 12 of the golf ball of the present invention
preferably has a diameter in the range of about 1.53 inches to
about 1.58 inches. In accordance to one aspect of the present
invention, the core is made from a polybutadiene rubber that has a
viscosity range from about 40 to about 60 Mooney. Polybutadiene
rubber with higher Mooney viscosity may also be used, so long as
the viscosity of the PBD does not reach a level where the high
viscosity PBD clogs or otherwise adversely interferes with the
manufacturing machinery. It is contemplated that PBD with viscosity
less than 65 Mooney can be used with the present invention. A
"Mooney" unit is a unit used to measure the plasticity of raw or
unvulcanized rubber. The plasticity in a "Mooney" unit is equal to
the torque, measured on an arbitrary scale, on a disk in a vessel
that contains rubber at a temperature of 100.degree. C. and rotates
at two revolutions per minute. The measurement of Mooney viscosity
is defined according to ASTM D-1646.
[0021] Golf ball cores made with mid to high Mooney viscosity PBD
material exhibit increased resiliency, hence distance, without
increasing the hardness of the ball. Such cores are soft, i.e.,
compression of about 50-80, and when these soft cores are
incorporated into golf balls such cores generate very low spin and
long distance when struck by a driver. Cores with compression in
the range of from about 30 to about 50 are also within the range of
the present invention.
[0022] In accordance to another aspect of the invention, the
addition of an organic sulfur compound to the core further
increases the resiliency and the coefficient of restitution of the
ball. Preferred organic sulfur compounds include, but not limited
to, pentachlorothiophenol (PCTP) and a salt of PCTP. A preferred
salt of PCTP is ZnPCTP. The utilization of PCTP and ZnPCTP in golf
ball cores to produce soft and fast cores is disclosed in
co-pending U.S. application Ser. No. 09/951,963 filed on Sep. 13,
2001, and is assigned to the same assignee as the present
invention. This co-pending application is incorporated by reference
herein, in its entirety. A suitable PCTP is sold by the Structol
Company under the tradename A95. ZnPCTP is commercially available
from eChinaChem.
[0023] Commercial sources of suitable mid to high Mooney PBD sold
by Bayer AG include CB 23, which has a Mooney viscosity of about 51
and is a preferred PBD. If desired, the polybutadiene can also be
mixed with other elastomers known in the art, such as natural
rubber, styrene butadiene, and/or isoprene in order to further
modify the properties of the core. When a mixture of elastomers is
used, the amounts of other constituents in the core composition are
based on 100 parts by weight of the total elastomer mixture.
[0024] Metal salt diacrylates, dimethacrylates, and
monomethacrylates suitable for use in this invention include those
where the metal is magnesium, calcium, zinc, aluminum, sodium,
lithium or nickel. Zinc diacrylate (ZDA) is preferred, but the
present invention is not limited thereto. ZDA provides golf balls
with a high initial velocity. Free radical initiators are also used
to promote cross-linking of the metal salt diacrylate,
dimethacrylate, or monomethacrylate and the polybutadiene. Free
radical initiators are used to promote cross-linking of the metal
salt diacrylate, dimenthacrylate, or monomethacrylate and the
polybutadiene rubber.
[0025] The core may also include fillers, added to the elastomeric
composition to adjust the density and/or specific gravity of the
core. Fillers useful in the golf ball core according to the present
invention include, for example, metal (or metal alloy) powders,
metal oxide, metal searates, particulate, carbonaceous materials,
and the like or blends thereof.
[0026] Antioxidants may also be included in the elastomer centers
produced according to the present invention. Antioxidants are
compounds, which prevent the breakdown of the elastomer.
Antioxidants useful in the present invention include, but are not
limited to, quinoline type antioxidants, amine type antioxidants,
and phenolic type antioxidants.
[0027] Other ingredients such as accelerators, processing aids,
processing oils, dyes and pigments, as well as other additives well
known to the skilled artisan may also be used in the present
invention in amounts sufficient to achieve the purpose for which
they are typically used.
[0028] The core 12 may be formed by mixing and forming the base
composition using conventional techniques. Detailed disclosures
concerning compositions of the core to achieve desired properties
in the ball are fully disclosed in co-pending patent application
Ser. No. 09/992,448. This patent application has been incorporated
by reference in its entirety.
[0029] Cover 16 is preferably tough, cut-resistant, and selected
from conventional materials used as golf ball covers based on the
desired performance characteristics. The cover may comprise one or
more layers. Suitable cover materials include ionomer resins, such
as Surlyn.RTM. available from DuPont, blends of ionomer resins,
thermoplastic or thermoset urethane, acrylic acid, methacrylic
acid, thermoplastic rubber polymers consisting of block copolymers
in which the elastomeric midblock of the molecule is an unsaturated
rubber or a saturated olefin rubber, e.g., Kraton.RTM. rubbers
available from Shell Chemical Co., polyethylene, and synthetic or
natural vulcanized rubber such as balata. Additionally, other
suitable core and cover materials are disclosed in U.S. Pat. No.
5,919,100 and international publications WO 00/23519 and WO
01/29129. These disclosures are incorporated by reference in their
entirety.
[0030] Most preferably, core 12 is made from a CB-23 polybutadiene
with ZnPCTP additive and tungsten filler, and cover 16 is made from
a composition comprising a thermoset urethane.
[0031] To prevent or minimize the penetration of moisture,
typically water vapor, into core 12 of golf ball 10, intermediate
layer 14 is a moisture vapor barrier layer preferably disposed
immediately around core 12. Preferably, moisture vapor barrier
layer 14 has a moisture vapor transmission rate that is lower than
that of the cover, and more preferably less than the moisture vapor
transmission rate of an ionomer resin such as Surlyn.RTM., which is
in the range of about 0.45 to about 0.95 gramsmm/m.sup.2day. The
moisture vapor transmission rate is defined as the mass of moisture
vapor that diffuses into a material of a given thickness per unit
area per unit time. The preferred standards of measuring the
moisture vapor transmission rate include ASTM F1249-90 entitled
"Standard Test Method for Water Vapor Transmission Rate Through
Plastic Film and Sheeting Using a Modulated Infrared Sensor," and
ASTM F372-94 entitled "Standard Test Method for Water Vapor
Transmission Rate of Flexible Barrier Materials Using an Infrared
Detection Technique," among others.
[0032] In accordance to one aspect of the invention, preferred
materials suitable for the intermediate moisture vapor barrier
layer 14 include copolymers of ethylene and methacrylic acid,
having an acid level from about 3% to about 25% by weight, more
preferably from about 4% to about 15%, and most preferably from
about 7% to about 11%, such as polyethylene methacrylic acid resins
commercially available under the tradename Nucrel.RTM. from DuPont.
Copolymers of ethylene and methacrylic acid have an advantage in
that these compounds typically have high melt flow index. The melt
flow index, also known as the melt index, as used herein has its
common and ordinary meaning, which is the amount, in grams, of a
thermoplastic resin which can be forced through an extrusion
rheometer orifice of 0.0825 inch diameter when subjected to a force
of 2.16 kg in 10 minutes at 190.degree. C. The melt flow index is
typically measured in accordance to the ASTM D 1238 standard. The
benefits of higher melt flow index include easier extrusion, higher
extrusion rate, higher flow during heat sealing, and the ability to
make thin films of moisture vapor barrier layer. Without limiting
the present invention to any particular theory, materials with
relatively high melt flow index have relatively low viscosity. Low
viscosity helps the materials spread evenly and thinly to produce a
thin film.
[0033] Suitable polyethylene methacrylic acid resins include, for
example, Nucrel.RTM. 599 resin, which contains 10% by weight of
acid and a melt flow index of 500 g/10 min, and Nucrel.RTM. 2940
which contains 19% acid by weight and a melt flow index of 395 g/10
min. These values, when compared to those of well-known ionomers
such as Surlyn.RTM., which have melt flow index typically in the
range of 1 g/10 min to 14 g/10 min, show that polyethylene
methacrylic acid resins have superior flow characteristic under
heat. Suitable polyethylene methacrylic acid resins exhibit melt
flow index in the range of about 1 g/10 min. to about 500 g/10
min., more preferably in the range of about 3 g/10 min. to about 60
g/10 min., and even more preferably less than about 35 g/10 min. or
in the range of about 5 g/10 min. to about 25 g/10 min.
[0034] The inventive use of copolymers of the ethylene and
methacrylic acid allows the production of very thin layers of
moisture vapor barrier, which in turn allows golf ball designers to
add a barrier layer to a well designed golf ball without
significantly changing the designed properties of the ball. This
simplifies the golf ball design process by not introducing a new
factor for consideration when moisture vapor barrier capability is
added to the ball.
[0035] The preferred materials, copolymers of ethylene and
methacrylic acid, exhibit water vapor barrier property of about
0.01 grams.mm/m.sup.2.day to 0.90 grams.mm/m.sup.2.day. The
thickness of intermediate layer 14 when made with the preferred
materials can be as thin as less than 0.030 inch, more preferably
from about 0.020 inch to about 0.005 inch. It can be readily
appreciated that at this small thickness intermediate layer 14 will
not significantly alter the properties of golf ball 10. More
specifically, the specific gravity of copolymers of ethylene and
methacrylic acid is between about 0.93 and about 0.95. With the
specific gravity in this range and with the above thickness, the
intermediate layer 14 would not have any significant effect on the
moment of inertia of ball 10. As used herein, specific gravity is
the ratio of the density of a substance to the density of water at
4.degree. C., which is 1.0g/cm.sup.3. Furthermore, the hardness of
copolymers of ethylene and methacrylic acid is available in the
range of about 42 to 63 Shore D. Hence, with the hardness in this
range and with the above thickness, the intermediate layer 14 would
not have a significant impact on the hardness or compression of
ball 10.
[0036] In accordance to another aspect of the invention, other
suitable materials for the intermediate water vapor barrier layer
include a blend of a copolymer of ethylene and methacrylic acid and
a suitable acid terpolymer of ethylene, a softening acrylate class
ester such as methyl acrylate, n-butyl-acrylate or
iso-butyl-acrylate, and a carboxylic acid such as acrylic acid or
methacrylic acid. Suitable examples of this acid terpolymer include
terpolymers of ethylene, methyl acrylate and acrylic acid (EMAAA),
commercially available under the tradename Escor.RTM. Acid
Terpolymers from Exxon Mobile Chemical. Such acid terpolymers blend
readily with copolymers of ethylene and methacrylic acid, and have
similar physical properties. For example, these acid terpolymers
have an acid content from about 6% to 6.5%, melt flow index in the
range of 5-20 g/10 min, specific gravity in the range of 0.94 to
0.95 and hardness in the range of 23-41 Shore D. Hence, a thin
layer of a blend comprising a copolymer of ethylene and methacrylic
acid and a terpolymer of ethylene, methyl acrylate and acrylic acid
would protect the golf ball core from water vapor invasion while
not significantly alter the other properties of the ball.
Preferably, this blend comprises 75% of a copolymer of ethylene and
methacrylic acid and 25 % of a suitable acid terpolymer, e.g.,
EMAAA terpolymer, or 25% of a copolymer of ethylene and methacrylic
acid and 75% of acid terpolymer, or 50% of each component.
Alternatively, the water vapor barrier layer may comprise the acid
terpolymer without a copolymer of ethylene methacrylic acid.
[0037] In accordance to another aspect of the invention, another
suitable material for the intermediate water vapor barrier layer is
a blend of a copolymer of ethylene and methacrylic acid and a
copolymer of ethylene and acrylic acid. Such copolymers of ethylene
and acrylic acid are commercially available as Primacor.RTM.
copolymers from Dow Plastics, and also have high acid content and
high melt flow index. Typical acrylic acid levels in commercial
copolymers of ethylene and acrylic acid range from about 3% and
about 20.5% and the melt flow index can be in the range of 300 g/10
min or higher. Similarly, the hardness level of this materials is
available in the range of 50 on the Shore D scale, and the specific
gravity is available in the range of 0.96. Hence, a thin layer of a
blend comprising a copolymer of ethylene and methacrylic acid and a
copolymer of ethylene and acrylic acid would protect the golf ball
core from water vapor invasion while not significantly alter the
other properties of the ball. Preferably, this blend comprises 25%
of a copolymer of ethylene and methacrylic acid and 75% of a
copolymer of ethylene and acrylic acid, or 75% of copolymer of
ethylene and methacrylic acid and 25% of copolymer of ethylene and
acrylic acid, or 50% of each copolymer. Alternatively, the water
vapor barrier may comprise a copolymer of ethylene and acrylic
acid, but not a copolymer of ethylene and methacrylic acid.
[0038] In accordance to another aspect of the invention, the
intermediate water vapor barrier layer 14 can be made from a blend
of (i) a copolymer of ethylene and methacrylic acid, (ii) a
terpolymer of ethylene, methyl acrylate and acrylic acid and (iii)
a copolymer of ethylene and acrylic acid. In accordance to another
aspect of the invention, the intermediate water vapor barrier may
also include one or more of the water vapor barrier materials
disclosed in co-pending patent application Ser. No. 09/973,342,
which is assigned to the same assignee as the present invention and
which is incorporated herein by reference. The suitable materials
discussed above are all non-ionomeric compounds, which are
compounds that are free of ions. Other non-ionomeric compounds may
also be suitable as a moisture vapor barrier layer.
[0039] Using CB-23 polybutadiene discussed above with the organic
sulfur compound ZnPCTP and tungsten fillers among other additives,
prototype cores 12 having 1.58 inch diameter with core compression
of 60, 65 and 75, respectively, were made. Each core then has a
thin layer of 0.020 inch of polyethylene methacrylic acid resin
(10.5% acid by weight) cased thereon. The subassembly then is
covered by a thermoset urethane cover. It has also been observed
that resins having lower levels of acid by weight generally achieve
more desirable water vapor barrier property.
[0040] The physical properties of the three prototypes are compared
to those of two known commercial balls, Pinnacle Gold LS and
Titleist Pro-V1, as shown below: TABLE-US-00001 Initial Hardness
Velocity Ball Weight on Cover Ball Type (ft/s) Compression (oz.)
(Shore D) CoR Pinnacle Gold LS 252.4 86 1.612 67 -- Titleist Pro-V1
253.6 90 1.611 58 -- Prototype A - 252.9 63 1.602 49 0.803 (60 core
compression) Prototype B - 253.4 71 1.606 51 0.809 (65 core
compression) Prototype C - 254.1 80 1.610 52 0.814 (75 core
compression)
[0041] The flight characteristics of the prototypes when struck by
various mechanical clubs are shown below: TABLE-US-00002 Pro 175
Standard Driver Average Driver (175 ft/s) (160 ft/s) (140 ft/s) 8
Iron Half Wedge Spin Speed Spin Speed Spin Speed Spin Speed Spin
Speed Ball Type (rev/min) (ft/s) (rev/min) (ft/s) (rev/min) (ft/s)
(rev/min) (ft/s) (rev/min) (ft/s) Pinnacle 2790 174.3 2962 159.4
3538 139.8 7641 114.9 4564 51.7 Gold LS Titleist 3137 175.0 3356
160.6 3960 140.1 7935 115.1 7020 52.9 Pro-V1 Prototype A- 2983
173.4 3076 159.5 3685 140.3 7245 115.0 6814 53.5 (60 core
compression) Prototype B- 3100 174.1 3118 159.8 3787 140.9 7458
114.8 6866 53.4 (65 core compression) Prototype C - 3208 174.7 3340
160.2 4404 141.7 7845 115.3 7093 53.2 (75 core compression)
[0042] Hence, the physical properties and flight characteristics of
balls made in accordance to the present invention are similar to
and in some cases exceed those of commercially successful
balls.
[0043] In accordance to another aspect of the invention, the
moisture vapor barrier layer 14 may be made by a number of methods.
A preferred method is the pre-formed semi-cured shells method,
where a quantity of mixed stock of the preferred moisture vapor
barrier material is placed into a compression mold and molded under
sufficient pressure, temperature and time to produce semi-cured,
semi-rigid half-shells. The half-shells are then place around a
core (solid or wound) and the sub-assembly is cured in another
compression molding machine to complete the curing process and to
reach the desirable size. A cover is then formed on the core
sub-assembly by any known method to complete the fabrication of the
ball.
[0044] As discussed above, the high melt flow index of the
preferred materials allows the construction of desirable thin
half-shells of water vapor barrier material, such that this layer
do not significantly alter the properties of the ball.
[0045] Other suitable manufacturing techniques include sheet stock
and vacuum, rubber injection molding, spraying, dipping, casting,
vacuum deposition, reaction injection molding, among others. A
two-pack casting method, such as the one disclosed in U.S. Pat. No.
5,897,884, may also be used. A simplified casting method using a
single blocked material to produce the moisture vapor barrier layer
14 can also be used. More particularly, this simplified method is
usable to make any castable components of the golf ball, including
the moisture vapor barrier layer, any intermediate layer, the
innermost core or any portion of the cover. The suitable
manufacturing methods discussed herein are discussed in more
details in co-pending patent application Ser. No. 09/973,342, which
has been incorporated by reference in its entirety.
[0046] While various descriptions of the present invention are
described above, it is understood that the various features of the
present invention can be used singly or in combination thereof.
Therefore, this invention is not to be limited to the specifically
preferred embodiments depicted therein.
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