Patent Application
20230312878
The present disclosure relates to a rubber composition, and particularly relates to a rubber composition providing a crosslinked rubber molded product with good softness and excellent resilience performance.
As a method for increasing a flight distance of a golf ball on driver shots, for example, there is a method of using a material having high resilience, Using the material having high resilience enhances the initial speed of the golf ball, thereby increasing the flight distance of the golf ball. Herein, examples of the material having high resilience include a rubber composition for forming a core, and a resin composition for forming an intermediate layer or cover.
As a golf ball having enhanced resilience performance, for example, JP 2012-125345 A discloses a golf ball having a constituting member, wherein at least a part of the constituting member is formed from a rubber composition containing (a) a base rubber, (b) a co-crosslinking agent, (c) a crosslinking initiator, and (d) an organic sulfur compound, and the organic sulfur compound is a derivative of thiophenols or diphenyl sulfides, and has a strong electron withdrawing substituent group.
Although various rubber compositions for enhancing the resilience have been proposed, there is still room for improvement in the resilience performance. The present disclosure has been achieved in view of the above circumstances, and an object of the present disclosure is to provide a novel rubber composition providing a crosslinked rubber molded product with good softness and excellent resilience performance.
The present disclosure that has solved the above problems provides a rubber composition containing (a) a base rubber, (b) a co-crosslinking agent, (c) a crosslinking initiator, and (d) an organic sulfur compound, wherein (d) the organic sulfur compound includes (d1) a compound represented by the formula (1) and/or (d2) a compound represented by the formula (2).
[In the formulae (1) and (2), R1 and R2 are identical to or different from each other, and represent an alkyl group having 1 or more carbon atoms, an aryl group having 6 or more carbon atoms, an aralkyl group having 6 or more carbon atoms, an alkoxy group having 1 or more carbon atoms, an alkylthio group having 1 or more carbon atoms, a perfluoroalkyl group having 1 or more carbon atoms, an amino group, a carboxy group, a hydrogen atom, or a halogen atom; R1 and R2 may bond to each other to form a cyclic structure, in this case, the cyclic structure may include at least one member selected from the group consisting of an oxygen atom, a nitrogen atom and a sulfur atom as a ring atom, and the ring atom may have a substituent group; and the substituent group of the ring atom includes at least one member selected from the group consisting of an alkyl group having 1 or more carbon atoms, an aryl group having 6 or more carbon atoms, an aralkyl group having 6 or more carbon atoms, an alkoxy group having 1 or more carbon atoms, an alkylthio group having 1 or more carbon atoms, a perfluoroalkyl group having 1 or more carbon atoms, an amino group, a carboxy group, and a halogen atom.) If the rubber composition according to the present disclosure is used, a crosslinked rubber molded product having good softness and excellent resilience performance is obtained.
The figure shows a relationship between the coefficient of restitution and the compression deformation amount of the crosslinked rubber composition.
The rubber composition according to the present disclosure contains (a) a base rubber, (b) a co-crosslinking agent, (c) a crosslinking initiator, and (d) an organic sulfur compound.
(d) The organic sulfur compound used in the present disclosure will be explained. (d) The organic sulfur compound includes (d1) a compound represented by the formula (1) and/or (d2) a compound represented by the formula (2). (d) The organic sulfur compound may be used solely, or two or more of them may be used in combination. If (d1) the compound represented by the formula (1) and/or (d2) the compound represented by the formula (2) is added in the rubber composition, the crosslinking reaction is accelerated and the crosslinking is densely formed, thus the resilience of the crosslinked molded product is improved without impairing the softness of the crosslinked molded product. It is noted that (d1) the compound represented by the formula (1) and (d2) the compound represented by the formula (2) are tautomer.
[In the formulae (1) and (2), R1 and R2 are identical to or different from each other, and represent an alkyl group having 1 or more carbon atoms, an aryl group having 6 or more carbon atoms, an aralkyl group having 6 or more carbon atoms, an alkoxy group having 1 or more carbon atoms, an alkylthio group having 1 or more carbon atoms, a perfluoroalkyl group having 1 or more carbon atoms, an amino group, a carboxy group, a hydrogen atom, or a halogen atom: R1 and R2 may bond to each other to form a cyclic structure, in this case, the cyclic structure may include at least one member selected from the group consisting of an oxygen atom, a nitrogen atom and a sulfur atom as a ring atom, and the ring atom may have a substituent group; and the substituent group of the ring atom includes at least one member selected from the group consisting of an alkyl group having 1 or more carbon atoms, an aryl group having 6 or more carbon atoms: an aralkyl group having 6 or more carbon atoms, an alkoxy group having 1 or more carbon atoms, an alkylthio group having 1 or more carbon atoms, a perfluoroalkyl group having 1 or more carbon atoms, an amino group, a carboxy group, and a halogen atom.]
Examples of the alkyl group having 1 or more carbon atoms represented by R1 and R2 include a linear alkyl group, a branched alkyl group, and a cyclic alkyl group. The alkyl group preferably has 1 or more carbon atoms, and preferably has 18 or less carbon atoms, more preferably has 12 or less carbon atoms.
Examples of the linear alkyl group include a methyl group, an ethyl group, a n-propyl group, a n-butyl group, and a n-pentyl group.
Examples of the branched alkyl group include an isopropyl group, an isobutyl group, a s-butyl group, a t-butyl group, and an isopentyl group.
Examples of the cyclic alkyl group include a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, and a cyclohexyl group.
The aryl group having 6 or more carbon atoms represented by R1 and R2 preferably has 18 or less carbon atoms, more preferably has 14 or less carbon atoms, Examples of the aryl group include a phenyl group, and a naphthyl group.
The aralkyl group having 6 or more carbon atoms represented by R1 and R2 preferably has 20 or less carbon atoms, more preferably has 14 or less carbon atoms. Examples of the aralkyl group include a benzyl group, a phenylethyl group, a phenylpropyl group, a phenylbutyl group, an α-cumyl group, and a 1-phenylethyl group.
The alkoxy group having 1 or more carbon atoms represented by R1 and R2 preferably has 18 or less carbon atoms, more preferably has 12 or less carbon atoms. Examples of the alkoxy group include a methoxy group, an ethoxy group, a propoxy group, a butoxy group, and a pentyloxy group.
The alkylthio group having 1 or more carbon atoms represented by R1 and R2 preferably has 18 or less carbon atoms, more preferably has 12 or less carbon atoms. Examples of the alkylthio group include a methylthio group, an ethylthio group, a propylthio group, a butylthio group, and a pentylthio group.
The perfluoroalkyl group having 1 or more carbon atoms represented by R1 and R2 preferably has 18 or less carbon atoms, more preferably has 12 or less carbon atoms. Examples of the perfluoroalkyl group include a trifluoromethyl group, a pentafluoroethyl group, and a heptafluoropropyl group.
Examples of the halogen atom represented by R1 and R2 include a fluorine atom, a chlorine atom, a bromine atom, and an iodine atom.
The cyclic structure formed by R1 and R2 bonding to each other preferably incudes one of a five-membered ring to a seven-membered ring. The cyclic structure may be either of an aromatic ring and a non-aromatic ring (d1) The compound represented by the formula (1) is preferably a compound represented by the formula (11). In addition, (d2) the compound represented by the formula (2) is preferably a compound represented by the formula (21).
[In the formulae (11) and (21) R11 to R14 are identical to or different from each other, and represent an alkyl group having 1 or more carbon atoms, an aryl group having 6 or more carbon atoms, an aralkyl group having 6 or more carbon atoms, an alkoxy group having 1 or more carbon atoms, an alkylthio group having 1 or more carbon atoms, a perfluoroalkyl group having 1 or more carbon atoms, an amino group, a carboxy group, a hydrogen atom, or a halogen atom.]
Examples of the alkyl group having 1 or more carbon atoms, the aryl group having 6 or more carbon atoms, the aralkyl group having 6 or more carbon atoms, the alkoxy group having 1 or more carbon atoms, the alkylthio group having 1 or more carbon atoms and the perfluoroalkyl group having 1 or more carbon atoms represented by R11 to R14 in the formulae (11) and (21) include those exemplified as R1 and R2 in the formulae (1) and (2).
R11 to R14 in the formulae (11) and (21) preferably include at least one member selected from the group consisting of an alkyl group having 1 to 12 carbon atoms, a perfluoroalkyl group having 1 to 12 carbon atoms, a halogen atom, and a hydrogen atom, (d1) The compound represented by the formula (1) is preferably at least one member selected from the group consisting of compounds represented by the formula (11-1) to the formula (11-12).
(d2) The compound represented by the formula (2) is preferably at least one member selected from the group consisting of compounds represented by the formula (21-1) to the formula (21-12).
The total amount of (d1) the compound represented by the formula (1) and (d2) the compound represented by the formula (2) is preferably 0.01 part by mass or more, more preferably 0.05 part by mass or more, and even more preferably 0.1 part by mass or more, and is preferably 20 parts by mass or less, more preferably 18 parts by mass or less, and even more preferably 15 parts by mass or less, with respect to 100 parts by mass of (a) the base rubber. If the total amount is 0.01 part by mass or more, the resilience is further enhanced, and if the total amount is 20 parts by mass or less, the softness is better.
Next, the other materials used for the rubber composition will be explained.
As (a) the base rubber, a natural rubber and/or a synthetic rubber can be used. Examples of the synthetic rubber include a diene rubber such as a polybutadiene rubber (BR), a polyisoprene rubber (IR), a styrene-polybutadiene rubber (SBR), a chloroprene rubber (CR), a butyl rubber (IIR), and an acrylonitrile-butadiene rubber (NBR); and a non-diene rubber such as an ethylene-propylene rubber (EPM), an ethylene-propylene-diene rubber (EPDM), a urethane rubber, a silicone rubber, an acrylic rubber, an epichlorohydrin rubber, a polysulfide rubber, a fluorinated rubber, and a chlorosulfonated polyethylene rubber. The rubber may be used solely, or two or more of them may be used in combination.
(a) The base rubber preferably contains the natural rubber and/or the diene rubber. The total amount of the natural rubber and/or the diene rubber in (a) the base rubber is preferably 50 mass % or more, more preferably 70 mass % or more, and even more preferably 90 mass % or more. It is also preferable that (a) the base rubber consists of the natural rubber and/or the diene rubber.
(a) The base rubber preferably includes a polybutadiene rubber, and particularly preferably includes a high-cis polybutadiene having a cis-1,4 bond in an amount of 40 mass % or more, preferably 80 mass % or more, and more preferably 90 mass % or more in view of its superior resilience. The amount of the high-cis polybutadiene in (a) the base rubber is preferably 50 mass % or more, more preferably 70 mass % or more. It is also preferable that (a) the base rubber consists of the high-cis polybutadiene.
The amount of the 1,2-vinyl bond in the high-cis polybutadiene is preferably 2.0 mass % or less, more preferably 1.7 mass % or less, and even more preferably 1.5 mass % or less. If the amount of the 1,2-vinyl bond is excessively great, the resilience may be lowered.
The high-cis polybutadiene is preferably a polybutadiene synthesized using a rare earth element catalyst. When a neodymium catalyst, which employs a neodymium compound that is a lanthanum series rare earth element compound, is used, a polybutadiene rubber having a high content of a cis-1,4 bond and a low content of a 1,2-vinyl bond is obtained with excellent polymerization activity. Such a polybutadiene rubber is particularly preferred.
The high-cis polybutadiene preferably has a molecular weight distribution Mw/Mn (Mw: weight average molecular weight, Mn: number average molecular weight) of 2.0 or more, more preferably 2.2 or more, even more preferably 2.4 or more, and most preferably 2.6 or more, and preferably has a molecular weight distribution Mw/Mn of 6.0 or less, more preferably 5.0 or less, even more preferably 4.0 or less, and most preferably 3.4 or less. If the molecular weight distribution (Mw/Mn) of the high-cis polybutadiene is excessively low, the processability deteriorates, if the molecular weight distribution (Mw/Mn) of the high-cis polybutadiene is excessively high, the resilience may be lowered, it is noted that the measurement of the molecular weight distribution is conducted by gel permeation chromatography (“HLC-8120GPC” available from Tosoh Corporation) using a differential refractometer as a detector under the conditions of column: GMHHXL (available from Tosoh Corporation), column temperature: 40° C., and mobile phase: tetrahydrofuran, and calculated by converting based on polystyrene standard.
The Mooney viscosity (ML1+4(100° C.)) of the high-cis polybutadiene is preferably 30 or more, more preferably 32 or more, and even more preferably 35 or more, and is preferably 140 or less, more preferably 120 or less, even more preferably 100 or less, and most preferably 80 or less. It is noted that the Mooney viscosity (ML1+4(100° C.)) in the present disclosure is a value measured according to JIS K6300 using an L rotor under the conditions of: a preheating time of 1 minute: a rotor revolution time of 4 minutes; and a temperature of 100° C.
(b) The co-crosslinking agent has an action of crosslinking a rubber molecule by graft polymerization to a base rubber molecular chain. (b) The co-crosslinking agent preferably includes an α,β-unsaturated carboxylic acid having 3 to 8 carbon atoms and/or a metal salt thereof. The α,β-unsaturated carboxylic acid used as (b) the co-crosslinking agent preferably has 3 to 8 carbon atoms, more preferably has 3 to 6 carbon atoms, and even more preferably has 3 or 4 carbon atoms. It is noted that the α,β-unsaturated carboxylic acid having 3 to 8 carbon atoms and/or the metal salt thereof may be used solely, or two or more of them may be used in combination, Examples of the α,β-unsaturated carboxylic acid having 3 to 8 carbon atoms include acrylic acid, methacrylic acid, fumaric acid, maleic acid and crotonic acid.
When the rubber composition contains only the α,β-unsaturated carboxylic acid having 3 to S carbon atoms as the co-crosslinking agent, the rubber composition preferably further contains (e) a metal compound. Neutralizing the α,β-unsaturated carboxylic acid having 3 to 8 carbon atoms with the metal compound in the rubber composition provides substantially the same effect as using the metal salt of the α,β-unsaturated carboxylic acid having 3 to 8 carbon atoms as the co-crosslinking agent.
Examples of the metal ion constituting the metal salt of the α,β-unsaturated carboxylic acid having 3 to 8 carbon atoms include a monovalent metal ion such as sodium, potassium and lithium; a divalent metal ion such as magnesium, calcium, zinc, barium and cadmium; a trivalent metal ion such as aluminum: and other metal ion such as tin and zirconium. The above metal component may be used solely or as a mixture of at least two of them. Among them, the divalent metal ion such as magnesium, calcium, zinc, barium and cadmium is preferably used as the metal component. This is because if the divalent metal salt of the α,β-unsaturated carboxylic acid having 3 to 8 carbon atoms is used, a metal crosslinking easily generates between the rubber molecules, Especially, the divalent metal salt is preferably the zinc salt of the α,β-unsaturated carboxylic acid having 3 to 8 carbon atoms, more preferably zinc acrylate, because use of such divalent metal salt enhances the resilience of the obtained golf ball. It is noted that when the α,β-unsaturated carboxylic acid having 3 to 8 carbon atoms is used together with the metal salt thereof as the co-crosslinking agent, (e) the metal compound can be used as an optional component.
When the metal is a divalent or trivalent metal, the metal salt of (b) the α,β-unsaturated carboxylic acid having 3 to 8 carbon atoms may further include other carboxylic acid than the α,β-unsaturated carboxylic acid having 3 to 8 carbon atoms, as the carboxylic acid moiety. Examples of the other carboxylic acid include a saturated carboxylic acid such as caprylic acid, capric acid, lauric acid, myristic acid, palmitic acid, stearic acid, arachidic acid, and behenic acid: and an unsaturated carboxylic acid such as palmitoleic acid, oleic acid, linoleic acid, linolenic acid, and arachidonic acid.
The amount of (b) the co-crosslinking agent is preferably 15 parts by mass or more, more preferably 18 parts by mass or more, and even more preferably 20 parts by mass or more, and is preferably 50 parts by mass or less, more preferably 45 parts by mass or less, and even more preferably 35 parts by mass or less, with respect to 100 parts by mass of (a) the base rubber. If the amount of (b) the co-crosslinking agent is 15 parts by mass or more, the member formed from the rubber composition has an appropriate hardness with a small amount of (c) the crosslinking initiator, and thus the crosslinked rubber molded product has further enhanced resilience. On the other hand, if the amount of (b) the co-crosslinking agent is 50 parts by mass or less, the member formed from the rubber composition is not excessively hard.
(c) The crosslinking initiator is blended to crosslink (a) the base rubber component. As (c) the crosslinking initiator, an organic peroxide is suitable. Specific examples of the organic peroxide include dicumyl peroxide, 1,1-bis(t-butylperoxy)-3,3,5-trimethylcyclohexane, 2,5-dimethyl-2,5-di(t-butylperoxy) hexane and di-t-butyl peroxide. These organic peroxides may be used solely or as a mixture of at least two of them. Among them, dicumyl peroxide is preferably used.
The amount of (c) the crosslinking initiator is preferably 0.2 part by mass or more, more preferably 0.5 part by mass or more, and even more preferably 0.7 part by mass or more, and is preferably 5.0 parts by mass or less, more preferably 2.5 parts by mass or less, even more preferably 2.0 parts by mass or less, and most preferably 0.9 part by mass or less, with respect to 100 parts by mass of (a) the base rubber. If the amount of (c) the crosslinking initiator is 0.2 part by mass or more, the crosslinked rubber molded product formed from the rubber composition is not excessively soft, and thus the resilience is better, and if the amount of (c) the crosslinking initiator is 5.0 parts by mass or less, the crosslinked rubber molded product formed from the rubber composition has an appropriate hardness, and thus the resilience and the durability are better.
The rubber composition may further contain (d3) another organic sulfur compound different from (d1) the compound represented by the formula (1) and (d2) the compound represented by the formula (2), Examples of (d3) other organic sulfur compounds include at least one member selected from the group consisting of thiophenols, thionaphthols, polysulfides, thiurams, thiocarboxylic acids, dithiocarboxylic acids, sulfenamides, dithiocarbamates, thiazoles, and metal salts thereof. As (d3) the other organic sulfur compounds, the thiophenols, thionaphthols, or the metal salt thereof are preferable, Examples of the thiophenols include thiophenol: thiophenols substituted with a fluoro group, such as 4-fluorothiophenol, 2,5-difluorothiophenol, 2,6-difluorothiophenol, 2,4,5-trifluorothiophenol, 2:4,5,6-tetrafluorothiophenol and pentafluorothiophenol; thiophenols substituted with a chloro group, such as 2-chlorothiophenol, 4-chlorothiophenol, 2,4-dichlorothiophenol, 2,5-dichlorothiophenol, 2,6-dichlorothiophenol, 2,4,5-trichlorothiophenol, 2,4,5,6-tetrachlorothiophenol and pentachlorothiophenol; thiophenols substituted with a bromo group, such as 4-bromothiophenol, 2,5-dibromothiophenol 2,6-dibromothiophenol, 2,4,5-tribromothiophenol, 2,4,5,6-tetrabromothiophenol and pentabromothiophenol; thiophenols substituted with an iodo group, such as 4-iodothiophenol, 2,5-diiodothiophenol, 2,6-diiodothiophenol, 2,4,5-triiodothiophenol, 2,4,5,6-tetraiodothiophenol and pentaiodothiophenol; and metal salts thereof. As the metal salt, zinc salt is preferable.
Examples of the thionaphthols (naphthalenethiols) include 2-thionaphthol, 1-thionaphthol, 1-chloro-2-thionaphthol, 2-chloro-1-thionaphthol, I-bromo-2-thionaphthol, 2-bromo-1-thionaphthol, I-fluoro-2-thionaphthol, 2-fluoro-1-thionaphthol, I-cyano-2-thionaphthol, 2-cyano-1-thionaphthol, I-acetyl-2-thionaphthol, 2-acetyl-1-thionaphthol, and metal salts thereof, Among them, 2-thionaphthol, 1-thionaphthol, and metal salts thereof are preferable. As the metal salt, a divalent metal salt is preferable, zinc salt is more preferable. Specific examples of the metal salt include zinc salt of 1-thionaphthol and zinc salt of 2-thionaphthol.
The polysulfides are organic sulfur compounds having a polysulfide bond, and examples thereof include disulfides, trisulfides, and tetrasulfides. As the polysulfides, diphenyl polysulfides are preferable, Examples of the diphenyl polysulfides include diphenyl disulfide; diphenyl disulfides substituted with a halogen group, such as bis(4-fluorophenyl)disulfide, bis(2,5-difluorophenyl)disulfide, bis(2,6-difluorophenyl)disulfide, bis(2,4,5-trifluorophenyl)disulfide, bis(2,4,5,6-tetrafluorophenyl)disulfide, bis(pentafluorophenyl)disulfide, bis(4-chlorophenyl)disulfide, bis(2,5-dichlorophenyl)disulfide, bis(2,6-dichlorophenyl)disulfide, bis(2,4,5-trichlorophenyl)disulfide, bis(2,4,5,6-tetrachiorophenyl)disulfide, bis(pentachlorophenyl)disulfide, bis(4-bromophenyl)disulfide, bis(2,5-dibromophenyl)disulfide, bis(2,6-dibromophenyl)disulfide, bis(2,4,5-tribromophenyl)disulfide, bis(2,4,5,6-tetrabromophenyl)disulfide, bis(pentabromophenyl)disulfide, bis(4-iodophenyl)disulfide, bis(2,5-diiodophenyl)disulfide, bis(2,6-diiodophenyl)disulfide, bis(2,4,5-triiodophenyl)disulfide, bis(2,4,5,6-tetraiodophenyl)disulfide and bis(pentaiodophenyl)disulfide; and diphenyl disulfides substituted with an alkyl group, such as bis(4-methylphenyl)disulfide, bis(2,4,5-trimethylphenyl)disulfide, bis(pentamethylphenyl)disulfide, bis(4-t-butylphenyl)disulfide, bis(2,4,5-tri-t-butylphenyl)disulfide, and bis(penta-t-butylphenyl)disulfide.
Examples of the thiurams include thiuram monosulfides such as tetramethylthiuram monosulfide; thiuram disulfides such as tetramethylthiuram disulfide, tetraethylthiuram disulfide and tetrabutylthiuram disulfide; and thiuram tetrasulfides such as dipentamethylenethiuram tetrasulfide. Examples of the thiocarboxylic acids include naphthalene thiocarboxylic acid, Examples of the dithiocarboxylic acids include naphthalene dithiocarboxylic acid, Examples of the sulfenamides include N-cyclohexyl-2-benzothiazole sulfenamide, N-oxydiethylene-2-benzothiazole sulfenamide, and N-t-butyl-2-benzothiazole sulfenamide.
(d3) Another organic sulfur compound may be used solely or as a mixture of at least two of them. As (d3) another the organic sulfur compound, the thiophenols and/or the metal salts thereof, the thionaphthols and/or the metal salts thereof, the diphenyl disulfides, and the thiuram disulfides are preferable, 2,4-dichlorothiophenol, 2,6-difluorothiophenol, 2,6-dichlorothiophenol, 2,6-dibromothiophenol, 2,6-diiodothiophenol. 2,4,5-trichlorothiophenol, pentachlorothiophenol, 1-thionaphthol, 2-thionaphthol, diphenyl disulfide, bis(2,6-difluorophenyl)disulfide, bis(2,6-dichlorophenyl)disulfide, bis(2,6-dibromophenyl)disulfide, bis(2,6-diiodophenyl)disulfide, and bis(pentabromophenyl)disulfide are more preferable.
The total amount of (d) the organic sulfur compound is preferably 0.01 part by mass or more, more preferably 0.05 part by mass or more, and even more preferably 0.1 part by mass or more, and is preferably 20 parts by mass or less, more preferably 18 parts by mass or less, and even more preferably 15 parts by mass or less, with respect to 100 parts by mass of (a) the base rubber. If the total amount of (d) the organic sulfur compound is less than 0.01 part by mass, the effect of adding (d) the organic sulfur compound may not be obtained, and thus the resilience of the crosslinked rubber molded product may not be enhanced. In addition, if the total amount of (d) the organic sulfur compound is more than 20 parts by mass, the obtained crosslinked rubber molded product has a great compression deformation amount and thus the resilience thereof may be lowered.
When the rubber composition used in the present disclosure contains only the α,β-unsaturated carboxylic acid having 3 to 8 carbon atoms as the co-crosslinking agent, the rubber composition preferably contains (e) a metal compound, (e) The metal compound is not particularly limited, as long as (e) the metal compound is capable of neutralizing (b) the α,β-unsaturated carboxylic acid having 3 to 8 carbon atoms in the rubber composition. Examples of (e) the metal compound include a metal hydroxide such as magnesium hydroxide, zinc hydroxide, calcium hydroxide, sodium hydroxide, lithium hydroxide, potassium hydroxide, and copper hydroxide; a metal oxide such as magnesium oxide, calcium oxide, zinc oxide, and copper oxide; and a metal carbonate such as magnesium carbonate, zinc carbonate, calcium carbonate, sodium carbonate, lithium carbonate, and potassium carbonate. As (e) the metal compound, the divalent metal compound is preferable, the zinc compound is more preferable. This is because the divalent metal compound reacts with the α,β-unsaturated carboxylic acid having 3 to 8 carbon atoms to form a metal crosslinking. In addition, if the zinc compound is used, the obtained crosslinked rubber molded product has higher resilience. (e) The metal compound may be used solely, or at least two of them may be used in combination. The amount of (e) the metal compound can be appropriately adjusted according to the desired neutralization degree of (b) the α,β-unsaturated carboxylic acid having 3 to 8 carbon atoms.
(f) Carboxylic Acid and/or Salt Thereof
The rubber composition may further contain (f) a carboxylic acid and/or a salt thereof. If the rubber composition contains (f) the carboxylic acid and/or the salt thereof, the hardness distribution of the obtained crosslinked rubber molded product is controlled. Examples of (f) the carboxylic acid and/or the salt thereof include an aliphatic carboxylic acid, an aliphatic carboxylic acid salt, an aromatic carboxylic acid and an aromatic carboxylic acid salt. (f) The carboxylic acid and/or the salt thereof may be used solely, or as a mixture of two or more of them. It is noted that (f) the carboxylic acid and/or the salt thereof excludes the α,β-unsaturated carboxylic acid having 3 to 8 carbon atoms and the metal salt thereof used as (b) the co-crosslinking agent.
The aliphatic carboxylic acid may be either a saturated aliphatic carboxylic acid (hereinafter sometimes referred to as “saturated fatty acid”) or an unsaturated aliphatic carboxylic acid (hereinafter sometimes referred to as “unsaturated fatty acid”). In addition, the aliphatic carboxylic acid may have a branched or cyclic structure. The saturated fatty acid preferably has 6 or more carbon atoms, and preferably has 24 or less carbon atoms, more preferably has 1$ or less carbon atoms, and even more preferably has 13 or less carbon atoms. The unsaturated fatty acid preferably has 6 or more carbon atoms, more preferably has 7 or more carbon atoms, and even more preferably has 8 or more carbon atoms, and preferably has 24 or less carbon atoms, more preferably has 18 or less carbon atoms: and even more preferably has 13 or less carbon atoms.
Examples of the aromatic carboxylic acid include a carboxylic acid having a benzene ring in the molecule, and a carboxylic acid having an aromatic heterocycle in the molecule. The aromatic carboxylic acid may be used solely, or two or more of them may be used in combination, Examples of the carboxylic acid having the benzene ring include an aromatic carboxylic acid having a carboxyl group directly bonding to a benzene ring, an aromatic-aliphatic carboxylic acid having an aliphatic carboxylic acid bonding to a benzene ring, a polynuclear aromatic carboxylic acid having a carboxyl group directly bonding to a fused benzene ring, and a polynuclear aromatic-aliphatic carboxylic acid having an aliphatic carboxylic acid bonding to a fused benzene ring, Examples of the carboxylic acid having the aromatic heterocycle include a carboxylic acid having a carboxyl group directly bonding to an aromatic heterocycle.
As the aliphatic carboxylic acid salt or aromatic carboxylic acid salt, a salt of the above mentioned aliphatic carboxylic acid or aromatic carboxylic acid can be used, Examples of the cation component of these salts include a metal ion, an ammonium ion, and an organic cation. The cation component may be used solely, or two or more of them may be used in combination, Examples of the metal ion include a monovalent metal ion such as sodium, potassium, lithium and silver; a divalent metal ion such as magnesium, calcium, zinc, barium, cadmium, copper, cobalt, nickel and manganese: a trivalent metal ion such as aluminum and iron; other ions such as tin, zirconium and titanium. Among them, the metal ion is preferably the divalent metal ion, more preferably magnesium, zinc, or calcium.
The organic cation is a cation having a carbon chain. The organic cation is not particularly limited, and examples thereof include an organic ammonium ion.
Examples of the organic ammonium ion include a primary ammonium ion such as a stearyl ammonium ion, a hexyl ammonium ion, an octyl ammonium ion and a 2-ethylhexyl ammonium ion; a secondary ammonium ion such as a dodecyl(lauryl) ammonium ion and an octadecyl(stearyl) ammonium ion; a tertiary ammonium ion such as a trioctyl ammonium ion; and a quaternary ammonium ion such as a dioctyldimethyl ammonium ion and a distearyldimethyl ammonium ion. These organic cations may be used solely, or two or more of them may be used in combination.
Examples of the aliphatic carboxylic acid and/or the salt thereof include a saturated fatty acid and/or a salt thereof, and an unsaturated fatty acid and/or a salt thereof. The saturated fatty acid and/or the salt thereof is preferable, and caprylic acid (octanoic acid), pelargonic acid (nonanoic acid), capric acid (decanoic acid), lauric acid, myristic acid, palmitic acid, stearic acid, behenic acid, and their potassium salt, magnesium salt, calcium salt, aluminum salt, zinc salt, iron salt, copper salt, nickel salt and cobalt salt, are preferable. As the unsaturated fatty acid and/or the salt thereof, palmitoleic acid, oleic acid, linoleic acid, arachidonic acid, and their potassium salt, magnesium salt, calcium salt, aluminum salt, zinc salt, iron salt, copper salt, nickel salt and cobalt salt, are preferable.
As the aromatic carboxylic acid and/or the salt thereof, benzoic acid, butylbenzoic acid, anisic acid(methoxybenzoic acid), dimethoxybenzoic acid, trimethoxybenzoic acid, dimethylaminobenzoic acid, chlorobenzoic acid, dichlorobenzoic acid, trichlorobenzoic acid, acetoxybenzoic acid, biphenylcarboxylic acid, naphthalenecarboxylic acid, anthracenecarboxylic acid, furancarboxylic acid, thenoic acid, and their potassium salt, magnesium salt, calcium salt, aluminum salt, zinc salt, iron salt, copper salt, nickel salt and cobalt salt, are particularly preferable.
The amount of (f) the carboxylic acid and/or the salt thereof is preferably 1 part by mass or more, more preferably 2 parts by mass or more, and even more preferably 3 parts by mass or more, and is preferably 30 parts by mass or less, more preferably 20 parts by mass or less, and even more preferably 15 parts by mass or less, with respect to 100 parts by mass of (a) the base rubber.
The rubber composition may contain additives such as a pigment, a filler for adjusting weight or the like, an antioxidant, a peptizing agent, and a softener, where necessary. In addition, the rubber composition may contain a rubber powder obtained by pulverizing a golf ball core or offcuts produced when preparing a core.
Examples of the pigment blended in the rubber composition include a white pigment, a blue pigment, and a purple pigment. As the white pigment, titanium oxide is preferably used. The type of titanium oxide is not particularly limited, but rutile type is preferably used because of its high opacity. In addition, the amount of titanium oxide is preferably 0.5 part by mass or more, more preferably 2 parts by mass or more, and is preferably 8 parts by mass or less, more preferably 5 parts by mass or less, with respect to 100 parts by mass of (a) the base rubber.
It is also preferred that the rubber composition contains both the white pigment and the blue pigment. The blue pigment is blended in order to cause white color to be vivid, and examples thereof include ultramarine blue, cobalt blue, and phthalocyanine blue. In addition, examples of the purple pigment include anthraquinone violet, dioxazine violet, and methyl violet.
The filler blended in the rubber composition is used as a weight adjusting agent for adjusting the mass of the obtained crosslinked rubber molded product. The filler may be blended where necessary. Examples of the filler include an inorganic filler such as zinc oxide, barium sulfate, calcium carbonate, magnesium oxide, tungsten powder, and molybdenum powder.
The amount of the antioxidant is preferably 0.1 part by mass or more and 1 part by mass or less with respect to 100 parts by mass of (a) the base rubber. In addition, the amount of the peptizing agent is preferably 0.1 part by mass or more and 5 parts by mass or less with respect to 100 parts by mass of (a) the base rubber.
The rubber composition used in the present disclosure is obtained by mixing and kneading (a) the base rubber, (b) the co-crosslinking agent, (c) the crosslinking initiator, (d) the organic sulfur compound, and other additives to be added where necessary. The kneading method is not particularly limited. For example, the kneading is conducted by using a conventional kneading machine such as a kneading roll, a banbury mixer, and a kneader.
The crosslinked rubber molded product according to the present disclosure is formed from the above-described rubber composition. The crosslinked rubber molded product is obtained by molding the kneaded rubber composition in a mold. The molding temperature is preferably 120° C. or more, more preferably 150° C. or more, and is preferably 250° C. or less. In addition, the molding pressure preferably ranges 2.9 MPa to 11.8 MPa. The molding time preferably ranges from 10 minutes to 60 minutes.
Examples of the crosslinked rubber molded product include sports goods such as a golf ball, a tennis ball and a grip; industrial goods such as a hose, a belt, and a mat; a sole, a tire, a resin additive, an anti-vibration rubber, and a fender. Examples of the golf ball include a golf ball comprising a constituent member formed from the above-described rubber composition,
The present disclosure includes a golf ball having a constituent member formed from the above-described rubber composition. In a preferable embodiment of the golf ball according to the present disclosure, the golf ball comprises a core and at least one cover layer covering the core, wherein at least a part of the core is formed from the above-described rubber composition. In the followings, the golf ball will be explained,
The core of the golf ball can be obtained by mixing and kneading the above-described rubber composition and molding the kneaded rubber composition in a mold. The molding condition is not particularly limited. Generally, the molding is carried out at a temperature ranging from 130° C. to 200° C. for 10 minutes to 60 minutes under a pressure ranging from 2.9 MPa to 11.8 MPa. For example, the golf ball rubber composition is preferably heated at a temperature ranging from 130° C. to 200° C. for 10 minutes to 60 minutes.
The core is preferably spherical. In addition, the core may have a single-layered structure or a multi-layered structure, and the single-layered structure is preferable, Unlike the core having the multi-layered structure, the core having the single-layered structure does not have an energy loss at the interface of the multi-layered structure when being hit, and thus has enhanced resilience.
The diameter of the core is preferably 34.8 mm or more, and is preferably 42.2 mm or less, more preferably 41.8 mm or less, even more preferably 41.2 mm or less, and most preferably 40.8 mm or less. If the diameter of the core is 34.8 mm or more, the cover is not excessively thick, and thus the resilience is better. On the other hand, if the diameter of the core is 42.2 mm or less, the cover is not excessively thin, and thus the cover functions better. When the core has a diameter ranging from 34.8 mm to 42.2 mm, the compression deformation amount (shrinking amount along the compression direction) of the core when applying a load from 98 N as an initial load to 1275 N as a final load to the core is preferably 2.0 mm or more, more preferably 2.3 mm or more, and even more preferably 2.5 mm or more, and is preferably 5.0 mm or less, more preferably 4.5 mm or less, and even more preferably 4.3 mm or less. If the compression deformation amount of the core is 2.0 mm or more, the shot feeling is better, and if the compression deformation amount of the core is 5.0 mm or less, the resilience is better,
The cover of the golf ball is formed from a cover composition containing a resin component, Examples of the resin component include an ionomer resin, a thermoplastic polyurethane elastomer having a trade name of “Elastollan (registered trademark)” available from BASF Japan Ltd., a thermoplastic polyamide elastomer having a trade name of “Pebax (registered trademark)” available from Arkema K, K, a thermoplastic polyester elastomer having a trade name of “Hytrel (registered trademark)” available from Du Pont-Toray Co., Ltd., and a thermoplastic styrene elastomer having a trade name of “TEFABLOC (registered trademark)” available from Mitsubishi Chemical Corporation.
In addition to the resin component, the cover composition may further contain a pigment component such as a white pigment (e.g. titanium oxide), a blue pigment and a red pigment, a weight adjusting agent such as zinc oxide, calcium carbonate and barium sulfate, a dispersant, an antioxidant, an ultraviolet absorber, a light stabilizer, a fluorescent material or fluorescent brightener, as long as they do not impair the performance of the cover.
Examples of the method for molding the cover of the golf ball include a method which comprises molding the cover composition into a hollow shell, covering the core with a plurality of the hollow shells and performing compression molding (preferably a method which comprises molding the cover composition into a hollow half-shell, covering the core with two of the half-shells and performing compression molding); and a method which comprises injection molding the cover composition directly onto the core.
The thickness of the cover is preferably 4.0 mm or less, more preferably 3.0 mm or less, and even more preferably 2.0 mm or less. If the thickness of the cover is 4.0 mm or less, the obtained golf ball has better resilience or shot feeling. The thickness of the cover is preferably 0.3 mm or more, more preferably 0.4 mm or more, and even more preferably 0.5 mm or more. If the thickness of the cover is less than 0.3 mm, the durability or wear resistance of the cover may be lowered. In the case that the cover is multi-layered, the total thickness of the multi-layered cover preferably falls within the above range.
Examples of the golf ball include a two-piece golf ball composed of a core and a single-layered cover covering the core; and a multiple-piece golf ball (including a three-piece golf ball) having a core and a cover covering the core and composed of at least two layers.
The golf ball preferably has a diameter ranging from 40 mm to 45 mm. In light of satisfying the regulation of US Golf Association (USGA), the diameter is particularly preferably 42.67 mm or more. In light of prevention of air resistance, the diameter is more preferably 44 mm or less, and particularly preferably 42.80 mm or less. In addition, the golf ball according to the present disclosure preferably has a mass of 40 g or more and 50 g or less. In light of obtaining greater inertia, the mass is more preferably 44 g or more, and particularly preferably 45.00 g or more. In light of satisfying the regulation of USGA, the mass is particularly preferably 45.93 g or less.
Next, the present disclosure will be described in detail by way of examples. However, the present disclosure is not limited to the examples described below. Various changes and modifications without departing from the spirit of the present disclosure are included in the scope of the present disclosure.
The deformation amount of the spherical molded product along the compression direction (shrinking amount of the spherical molded product along the compression direction), when applying a load from 98 N as an initial load to 1275 N as a final load to the spherical molded product, was measured.
A metal cylindrical object with a mass of 198.4 g was allowed to collide with each spherical molded product at a speed of 40 m/sec, and the speeds of the cylindrical object and the spherical molded product before and after the collision were measured. Based on the speed and the mass of each object, the coefficient of restitution of each spherical molded product was calculated. The measurement was conducted by using twelve samples for each spherical molded product, and the average value thereof was adopted as the coefficient of restitution of the spherical molded product.
The rubber compositions having the formulations shown in Table 1 were kneaded with a kneading roll, and heat pressed at a temperature of 170° C. for 20 minutes in upper and lower molds, each having a hemispherical cavity, to obtain spherical molded products having a diameter of 40.86 mm.
Table 1 shows the compression deformation amount and the coefficient of restitution of each spherical molded product. In addition, the figure shows the relationship between the compression deformation amount and the coefficient of restitution of each spherical molded product. As shown in the figure, there is a tendency that the amount of the co-crosslinking agent is greater, the resilience performance is higher, and the compression deformation amount is smaller, when the materials contained in the rubber composition are same, Thus, it can be said that if the line connecting the plots of the spherical molded product formed from the same materials is located at the upper right of the graph, the spherical molded product has higher softness and more excellent resilience performance.
The spherical molded products No. 1 to 3 are formed from a rubber composition neither containing (d1) the compound represented by the formula (1) nor (d2) the compound represented by the formula (2) as (d) the organic sulfur compound. The spherical molded products No. 4 to 11 are formed from a rubber composition containing (d1) the compound represented by the formula (1) and/or (d2) the compound represented by the formula (2) as (d) the organic sulfur compound. It can be seen from
The present disclosure (1) is a rubber composition containing (a) a base rubber, (b) a co-crosslinking agent, (c) a crosslinking initiator, and (d) an organic sulfur compound, wherein (d) the organic sulfur compound includes (d1) a compound represented by the formula (1) and/or (d2) a compound represented by the formula (2).
[In the formulae (1) and (2), R1 and R2 are identical to or different from each other, and represent an alkyl group having 1 or more carbon atoms, an aryl group having 6 or more carbon atoms, an aralkyl group having 6 or more carbon atoms, an alkoxy group having 1 or more carbon atoms, an alkylthio group having 1 or more carbon atoms, a perfluoroalkyl group having 1 or more carbon atoms, an amino group, a carboxy group, a hydrogen atom, or a halogen atom; R1 and R2 may bond to each other to form a cyclic structure, in this case, the cyclic structure may include at least one member selected from the group consisting of an oxygen atom, a nitrogen atom and a sulfur atom as a ring atom, and the ring atom may have a substituent group; and the substituent group of the ring atom includes at least one member selected from the group consisting of an alkyl group having 1 or more carbon atoms, an aryl group having 6 or more carbon atoms, an aralkyl group having 6 or more carbon atoms, an alkoxy group having 1 or more carbon atoms, an alkylthio group having 1 or more carbon atoms, a perfluoroalkyl group having 1 or more carbon atoms, an amino group, a carboxy group, and a halogen atom.]
The present disclosure (2) is the rubber composition according to the present disclosure (1), wherein in the formula (1) and the formula (2), R1 and R2 bond to each other to form a cyclic structure, and the cyclic structure has one of a five-membered ring to a seven-membered ring.
The present disclosure (3) is the rubber composition according to the present disclosure (1) or (2), wherein (d1) the compound represented by the formula (1) is a compound represented by the formula (11), and (d2) the compound represented by the formula (2) is a compound represented by the formula (21),
[In the formulae (11) and (21), R11 to R14 are identical to or different from each other, and represent an alkyl group having 1 or more carbon atoms, an aryl group having 6 or more carbon atoms, an aralkyl group having 6 or more carbon atoms, an alkoxy group having 1 or more carbon atoms, an alkylthio group having 1 or more carbon atoms, a perfluoroalkyl group having 1 or more carbon atoms, an amino group, a carboxy group, a hydrogen atom, or a halogen atom.]
The present disclosure (4) is the rubber composition according to any one of the present disclosures (1) to (3), wherein a total amount of (d1) the compound represented by the formula (1) and (d2) the compound represented by the formula (2) ranges from 0.01 part by mass to 20 parts by mass with respect to 100 parts by mass of (a) the base rubber.
The present disclosure (5) is the rubber composition according to any one of the present disclosures (1) to (4), wherein an amount of (b) the co-crosslinking agent ranges from 15 parts by mass to 50 parts by mass with respect to 100 parts by mass of (a) the base rubber.
The present disclosure (5) is a crosslinked rubber molded product formed from the rubber composition according to any one of the present disclosures (1) to (5).
The present disclosure (7) is a golf ball having a constituent member formed from the rubber composition according to any one of the present disclosures (1) to (5).
If the rubber composition according to the present disclosure is used, a crosslinked rubber molded product having excellent resilience performance is obtained, Thus, the rubber composition according to the present disclosure is used for sports goods such as a golf ball, a tennis ball and a grip: industrial goods such as a hose, a belt, and a mat; a sole, a tire, a resin additive, anti-vibration rubber, and a fender, and so on.
This application is based on Japanese patent application No. 2022-053522 filed on Mar. 29, 2022, the content of which is hereby incorporated by reference.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2022-053522 | Mar 2022 | JP | national |
