[go: up one dir, main page]

WO2018101361A1 - Composition de caoutchouc, et pneumatique - Google Patents

Composition de caoutchouc, et pneumatique Download PDF

Info

Publication number
WO2018101361A1
WO2018101361A1 PCT/JP2017/042902 JP2017042902W WO2018101361A1 WO 2018101361 A1 WO2018101361 A1 WO 2018101361A1 JP 2017042902 W JP2017042902 W JP 2017042902W WO 2018101361 A1 WO2018101361 A1 WO 2018101361A1
Authority
WO
WIPO (PCT)
Prior art keywords
mass
range
rubber composition
hydrocarbon resin
monomer unit
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/JP2017/042902
Other languages
English (en)
Japanese (ja)
Inventor
淳 野澤
涼嗣 亀山
祥史 丸山
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Zeon Corp
Original Assignee
Zeon Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Zeon Corp filed Critical Zeon Corp
Priority to JP2018554211A priority Critical patent/JP7081495B2/ja
Publication of WO2018101361A1 publication Critical patent/WO2018101361A1/fr
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B60—VEHICLES IN GENERAL
    • B60C—VEHICLE TYRES; TYRE INFLATION; TYRE CHANGING; CONNECTING VALVES TO INFLATABLE ELASTIC BODIES IN GENERAL; DEVICES OR ARRANGEMENTS RELATED TO TYRES
    • B60C1/00—Tyres characterised by the chemical composition or the physical arrangement or mixture of the composition
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F210/00—Copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
    • C08F210/14—Monomers containing five or more carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F212/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F232/00—Copolymers of cyclic compounds containing no unsaturated aliphatic radicals in a side chain, and having one or more carbon-to-carbon double bonds in a carbocyclic ring system
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F236/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds
    • C08F236/02—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds
    • C08F236/04—Copolymers of compounds having one or more unsaturated aliphatic radicals, at least one having two or more carbon-to-carbon double bonds the radical having only two carbon-to-carbon double bonds conjugated
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00—Use of inorganic substances as compounding ingredients
    • C08K3/34—Silicon-containing compounds
    • C08K3/36—Silica
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/18—Homopolymers or copolymers of hydrocarbons having four or more carbon atoms
    • C08L23/20—Homopolymers or copolymers of hydrocarbons having four or more carbon atoms having four to nine carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L9/00—Compositions of homopolymers or copolymers of conjugated diene hydrocarbons
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02T—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO TRANSPORTATION
    • Y02T10/00—Road transport of goods or passengers
    • Y02T10/80—Technologies aiming to reduce greenhouse gasses emissions common to all road transportation technologies
    • Y02T10/86—Optimisation of rolling resistance, e.g. weight reduction 

Definitions

  • the present invention relates to a rubber composition having excellent processability and excellent balance between rolling resistance and wet grip performance.
  • a cross-linked product of a rubber composition in which silica is added to a rubber component as a filler constitutes a tire compared to a cross-linked product of a rubber composition in which carbon black is mixed. In this case, the rolling resistance is reduced. Therefore, a tire excellent in fuel efficiency can be obtained by constituting a tire using a crosslinked product of a rubber composition containing silica.
  • Patent Document 1 for the purpose of improving tire rolling resistance and wet grip properties, a specific amount of a softening agent having a specific structure and a specific amount of a hydrocarbon resin are added to a rubber component. Is disclosed.
  • the present invention has been made in view of the above problems, and has as its main object to provide a rubber composition that is excellent in workability and excellent in the balance between rolling resistance and wet grip performance.
  • a hydrocarbon resin containing a monomer unit in a predetermined ratio and having a predetermined characteristic such as a weight average molecular weight within a predetermined range is improved in processability, rolling resistance and wet grip performance for a rubber composition.
  • the present invention has been completed by finding that it is involved in a well-balanced improvement of both performances.
  • a rubber composition comprising 1 part by mass to 30 parts by mass of a hydrocarbon resin and 80 parts by mass to 200 parts by mass of silica based on 100 parts by mass of a diene rubber.
  • the resin includes an aliphatic monomer unit and an aromatic monomer unit, and the aromatic unit of the monomer unit having a structure in which two or more cyclic structures are bonded among the aromatic monomer units.
  • a rubber having a content in a body unit of 50% by mass or more, a weight average molecular weight (Mw) in a range of 700 to 6000, and a softening point in a range of 80 ° C. to 150 ° C.
  • Mw weight average molecular weight
  • the hydrocarbon resin is composed of 10 to 60% by mass of 1,3-pentadiene monomer units, 1 to 30% by mass of alicyclic monoolefin monomer units having 4 to 6 carbon atoms, and 4 to 4 carbon atoms.
  • 8 acyclic monoolefin monomer unit 1% by mass to 50% by mass, alicyclic diolefin monomer unit 0% by mass to 10% by mass, and the above aromatic monomer unit 0.1% by mass to 50% by weight
  • the number average molecular weight (Mn) is in the range of 400 to 3000
  • the Z average molecular weight (Mz) is in the range of 1500 to 20000
  • the ratio of the weight average molecular weight to the number average molecular weight (Mw / Mn) is preferably in the range of 1.0 to 4.0
  • the ratio of the Z average molecular weight to the weight average molecular weight (Mz / Mw) is preferably in the range of 1.0 to 4.0.
  • the monomer having a structure in which two or more cyclic structures are bonded is at least one selected from the group consisting of naphthalene compounds, fluorene compounds, biphenyl compounds, anthracene compounds, phenanthrene compounds, indene compounds, and benzothiophene compounds. It is preferable.
  • the hydrocarbon resin has a mixed aniline point value of 25 ° C. to 100 ° C. measured at the lowest temperature at which a mixed solution (volume ratio 2: 1: 1) of aniline, methylcyclohexane and the hydrocarbon resin exists as a uniform solution. It is preferably within the range of ° C.
  • a pneumatic tire characterized by using the above rubber composition for a tread.
  • the present invention has an effect that it is possible to provide a rubber composition which is excellent in workability and has a good balance between rolling resistance and wet grip performance.
  • the present invention relates to a rubber composition and a pneumatic tire using it as a tread.
  • a rubber composition and a pneumatic tire of the present invention will be described in detail.
  • the rubber composition of the present invention is a rubber composition comprising 1 part by mass to 30 parts by mass of a hydrocarbon resin and 80 parts by mass to 200 parts by mass of silica with respect to 100 parts by mass of a diene rubber.
  • the hydrocarbon resin includes an aliphatic monomer unit and an aromatic monomer unit, and the aromatic unit is a monomer unit having a structure in which two or more cyclic structures are bonded among the aromatic monomer units.
  • the content in the group monomer unit is 50 mass% or more, the weight average molecular weight (Mw) is in the range of 700 to 6000, and the softening point is in the range of 80 ° C. to 150 ° C. It is what.
  • the rubber composition includes an aliphatic monomer unit and an aromatic monomer unit, and has a structure in which two or more cyclic structures are bonded among the aromatic monomer units.
  • a rubber composition having excellent workability and excellent balance of rolling resistance and wet grip performance can be obtained, but as follows.
  • the hydrocarbon resin can have a weight average molecular weight (Mw) that is moderately low and a softening point that is moderately high. For this reason, the hydrocarbon resin has excellent compatibility with the diene rubber, and for example, uniform mixing with the diene rubber is facilitated, so that the obtained rubber composition has excellent processability.
  • the loss factor tan ⁇ at 60 ° C. of the crosslinked product can be lowered, and the loss coefficient tan ⁇ at 0 ° C. can be appropriately increased.
  • a pneumatic tire using such a rubber composition as a tread is manufactured, a pneumatic tire or the like having an excellent balance of rolling resistance and wet grip performance can be formed.
  • the rubber composition further includes a predetermined amount of silica, whereby a rubber composition having an excellent balance between rolling resistance and wet grip performance can be obtained.
  • the compounding amount of the silica is less than 80 parts by mass, the wet grip performance is deteriorated, and when it is more than 200 parts by mass, the rolling resistance is deteriorated.
  • the amount of silica is 80 parts by mass or more, processability is deteriorated. Therefore, the rubber composition contains a predetermined amount of the hydrocarbon resin together with silica, thereby suppressing deterioration in workability and improving the balance between rolling resistance and wet grip performance.
  • the rubber composition contains a predetermined amount of the hydrocarbon resin together with silica with respect to the diene rubber, so that the processability is excellent and the balance between rolling resistance and wet grip performance is excellent. It becomes a thing.
  • the rubber composition of the present invention contains a diene rubber, a hydrocarbon resin and silica.
  • a diene rubber a diene rubber
  • a hydrocarbon resin a hydrocarbon resin
  • silica silica
  • hydrocarbon resin includes an aliphatic monomer unit and an aromatic monomer unit.
  • Aromatic monomer unit The aromatic monomer unit in the present invention includes a monomer unit having a structure in which two or more cyclic structures are bonded.
  • the monomer constituting the monomer unit having a structure in which two or more cyclic structures are bonded is usually one or more aliphatic carbon-carbon unsaturated bonds in the molecular structure and two or more cyclic structures. Those having a structure in which are bonded to each other are preferably used.
  • any structure that includes one or more aromatic rings among the two or more cyclic structures may be used. It may contain a ring and a non-aromatic ring structure.
  • the aliphatic carbon-carbon unsaturated bond is not particularly limited as long as it has radical polymerizability, and a vinyl group can be preferably used.
  • the aliphatic carbon-carbon unsaturated bond may be included as a part of the cyclic structure, such as a vinylene group included in a five-membered ring of indene, or a vinyl group included in 1-vinylnaphthalene. In this way, it may be bonded to the ring structure.
  • it is particularly preferable that the aliphatic carbon-carbon unsaturated bond is included as a part of the cyclic structure. This is because the polymerizability, the molecular weight, and the controllability of the softening point are excellent.
  • the cyclic structure is a non-aromatic ring structure.
  • the number of carbons of the cyclic structure including the aliphatic carbon-carbon unsaturated bond as a part thereof has desired characteristics.
  • Any hydrocarbon resin can be used as long as it can be formed.
  • it can be in the range of 4 to 8, but is preferably in the range of 4 to 6.
  • the aliphatic carbon-carbon unsaturated bond is included as a part of the indene five-membered ring as described above, and
  • the cyclic structure containing a group carbon-carbon unsaturated bond as a part thereof has 5 carbon atoms.
  • the aliphatic carbon-carbon unsaturated bond is bonded to the cyclic structure like a vinyl group contained in 1-vinylnaphthalene. They may be directly bonded to each other, or may be bonded to the cyclic structure via a spacer, such as an allyl group contained in allylnaphthalene.
  • the spacer examples include a hydrocarbon group bonded to a vinyl group such as a 2-propenyl group (allyl group) and 1-butenyl group, a carbonyl group bonded to a vinyl group such as an acryloyl group and a methacryloyl group. it can.
  • the number of carbon atoms of the spacer is not particularly limited as long as it can form a hydrocarbon resin having desired characteristics, and can be within a range of, for example, 1 to 3.
  • the number of the aliphatic carbon-carbon unsaturated bond contained in the monomer having a structure in which two or more cyclic structures are bonded is usually one or more, for example, within the range of 1 to 2. Although it is possible, one is preferred. Note that the number of the aliphatic carbon-carbon unsaturated bonds is the number of each monomer when two or more types of monomers are included as monomers having a structure in which two or more cyclic structures are combined. It refers to the number of aliphatic carbon-carbon unsaturated bonds involved.
  • a structure in which two or more cyclic structures are bonded includes a structure in which a cyclic structure forms a condensed ring group such as a naphthalene structure, a fluorene structure, an anthracene structure, a phenanthrene structure, a benzothiophene structure, an indene, or the like, a biphenyl structure A group in which the cyclic structures are directly connected by a single bond, such as a terphenyl structure, or a group in which the cyclic structures form a condensed ring group and a group in which the cyclic structures are directly connected by a single bond The thing containing both of things can be mentioned.
  • Examples of the structure in which two or more cyclic structures are bonded include only an aromatic ring include naphthalene structure, biphenyl structure, anthracene structure, phenanthrene structure, benzothiophene structure, and the like.
  • Examples of those containing a family ring structure include a fluorene structure and an indene structure.
  • the structure in which two or more cyclic structures are combined includes an aromatic ring and a non-aromatic ring structure. Since the structure in which two or more cyclic structures are combined includes an aromatic ring and a non-aromatic ring structure as a cyclic structure, the hydrocarbon resin is excellent in workability and has rolling resistance and wet grip performance. This is because a rubber composition having an excellent balance can be provided.
  • the cyclic structure includes oxygen, nitrogen, sulfur, such as a benzothiophene structure, in addition to a ring structure formed only by carbon, such as a naphthalene structure, a fluorene structure, a biphenyl structure, an anthracene structure, a phenanthrene structure, and the like. It may have a heterocyclic ring containing atoms other than carbon such as.
  • the cyclic structure may have a substituent.
  • substituents include halogen atoms (F, Cl, Br, I), hydroxyl groups, carboxyl groups, cyano groups, amino groups, nitro groups, sulfo groups, carbamoyl groups, sulfamoyl groups, ureido groups, alkyl groups, alkenyls.
  • alkynyl group alkynyl group, aliphatic acyl group, aliphatic acyloxy group, alkoxy group, alkoxycarbonyl group, alkoxycarbonylamino group, alkylthio group, alkylsulfonyl group, aliphatic amide group, aliphatic sulfonamido group, aliphatic substituted amino group
  • an aliphatic substituted carbamoyl group, an aliphatic substituted sulfamoyl group, an aliphatic substituted ureido group, and the like can be given.
  • the number of the cyclic structures included in the structure in which the two or more cyclic structures are combined may be two or more, and may be in the range of 2 to 6, but in the range of 2 to 3. Is preferred.
  • the monomer having a structure in which two cyclic structures are bonded include 1-vinylnaphthalene, 4-vinylbiphenyl, and indene.
  • Specific examples of the monomer having a structure in which three cyclic structures are bonded include 2,7-divinylfluorene and 9-vinylanthracene.
  • the monomer having a structure in which two or more cyclic structures are bonded is preferably a naphthalene compound, a fluorene compound, a biphenyl compound, an anthracene compound, a phenanthrene compound, an indene compound and a benzothiophene compound.
  • an indene compound is preferable, and indene is particularly preferable.
  • the hydrocarbon resin has excellent workability and a rubber composition having excellent balance of rolling resistance and wet grip performance. Because they can give things.
  • naphthalene compound examples include those having a naphthalene structure and one or more aliphatic carbon-carbon unsaturated bonds in the molecular structure, such as 1-vinylnaphthalene, 2-vinylnaphthalene, allylnaphthalene, butenyl. Naphthalene etc. can be mentioned.
  • fluorene compound examples include those having a fluorene structure and one or more aliphatic carbon-carbon unsaturated bonds in its molecular structure, such as 2,7-divinylfluorene, 2-vinylfluorene, allylfluorene, Examples include butenyl fluorene.
  • biphenyl compound examples include those having a biphenyl structure and one or more aliphatic carbon-carbon unsaturated bonds in the molecular structure, such as 4-vinylbiphenyl, 4-vinyl-p-terphenyl, etc. Can be mentioned.
  • anthracene compounds include those having an anthracene structure and one or more aliphatic carbon-carbon unsaturated bonds in the molecular structure, such as 9-vinylanthracene, 2-vinylanthracene, 9,10-divinyl.
  • Anthracene, allyl anthracene, butenyl anthracene, etc. can be mentioned.
  • phenanthrene compound examples include those having a phenanthrene structure and one or more aliphatic carbon-carbon unsaturated bonds in the molecular structure, such as 9-vinylphenanthrene and 3-vinylphenanthrene. .
  • the indene compound may be any compound having an indene structure in its molecular structure.
  • indene methylindene, ethylindene, propylindene, butylindene, t-butylindene, sec-butylindene, n-pentyl
  • alkyl-substituted indenes such as indene, 2-methyl-butylindene, 3-methyl-butylindene, n-hexylindene, 2-methyl-pentylindene, 3-methyl-pentylindene, 4-methyl-pentylindene, etc. Can do.
  • benzothiophene compound examples include those having a benzothiophene structure and one or more aliphatic carbon-carbon unsaturated bonds in the molecular structure.
  • benzothiophene compound examples include those having a benzothiophene structure and one or more aliphatic carbon-carbon unsaturated bonds in the molecular structure.
  • 5-vinylbenzothiophene, 2-vinyldibenzothiophene, etc. Can be mentioned.
  • the monomer having a structure in which two or more cyclic structures are bonded may include only one type of monomer, or may include two or more types of monomers mixed together. Good.
  • the monomer having a structure in which two or more cyclic structures are bonded can be a mixture of 9-vinylanthracene which is an anthracene compound and 9-vinylphenanthrene which is a phenanthrene compound.
  • the content of the monomer unit having a structure in which two or more cyclic structures are combined in the aromatic monomer unit may be 50% by mass or more, and is in the range of 55% by mass to 99.9% by mass. In particular, it is preferably in the range of 58% by mass to 99.85% by mass, and particularly preferably in the range of 60% by mass to 99.8% by mass. It is because the said hydrocarbon resin can give the rubber composition excellent in workability and the balance of rolling resistance and wet grip performance because the said content is in the above-mentioned range.
  • the aromatic monomer unit includes a monomer unit having a structure in which two or more cyclic structures are bonded.
  • a monomer unit containing only a cyclic structure that is, a monomer unit containing only one aromatic ring as the cyclic structure may be included.
  • Examples of the monomer constituting the monomer unit containing only one cyclic structure include styrene, ⁇ -methylstyrene, vinyltoluene and the like.
  • the hydrocarbon resin can provide a rubber composition having excellent workability and excellent balance between rolling resistance and wet grip performance.
  • it may be in the range of 0.1% by mass to 50% by mass, preferably in the range of 5% by mass to 45% by mass, and more preferably in the range of 8% by mass to 43% by mass. It is preferably within the range of 10% by mass to 40% by mass. It is because the said hydrocarbon resin can give the rubber composition excellent in workability and the balance of rolling resistance and wet grip performance because the said content is in the above-mentioned range.
  • Aliphatic monomer unit As the aliphatic monomer unit in the present invention, it is possible to provide a rubber composition that exhibits the above-mentioned predetermined characteristics, is excellent in workability, and has an excellent balance of rolling resistance and wet grip performance. Any hydrocarbon resin can be used as long as it can be formed.
  • Such an aliphatic monomer unit may be any unit that does not contain an aromatic ring, such as a 1,3-pentadiene monomer unit, an alicyclic monoolefin monomer having 4 to 6 carbon atoms.
  • a unit, an acyclic monoolefin monomer unit having 4 to 8 carbon atoms, an alicyclic diolefin monomer unit, and the like can be preferably included.
  • 1,3-pentadiene monomer unit 10 mass% to 60 mass%, C 4-6 alicyclic monoolefin monomer unit 1 mass % To 30% by mass, 1 to 50% by mass of acyclic monoolefin monomer units having 4 to 8 carbon atoms, and 0 to 10% by mass of alicyclic diolefin monomer units. it can.
  • the content of 1,3-pentadiene monomer units in the hydrocarbon resin is a hydrocarbon resin that is excellent in processability and can provide a rubber composition with a good balance of rolling resistance and wet grip performance.
  • Any material can be used as long as it can be obtained.
  • it can be in the range of 10% by mass to 60% by mass, preferably in the range of 15% by mass to 55% by mass, and more preferably 20% by mass to It is preferably in the range of 50% by mass, and particularly preferably in the range of 25% by mass to 48% by mass. It is because the said hydrocarbon resin can give the rubber composition excellent in workability and the balance of rolling resistance and wet grip performance because the said content is in the above-mentioned range.
  • the cis / trans isomer ratio in 1,3-pentadiene is not particularly limited and may be any ratio.
  • the alicyclic monoolefin having 4 to 6 carbon atoms is a hydrocarbon compound having 4 to 6 carbon atoms having one aliphatic carbon-carbon unsaturated bond and a non-aromatic ring structure in its molecular structure. is there.
  • Specific examples of the alicyclic monoolefin having 4 to 6 carbon atoms include cyclobutene, cyclopentene, cyclohexene, methylcyclobutene, and methylcyclopentene.
  • the content of the alicyclic monoolefin monomer unit having 4 to 6 carbon atoms in the hydrocarbon resin is to provide a rubber composition having excellent workability and a good balance between rolling resistance and wet grip performance.
  • Any hydrocarbon resin can be used as long as it can be obtained.
  • it can be in the range of 1% by mass to 30% by mass, and preferably in the range of 3% by mass to 28% by mass.
  • it is preferably in the range of 5% by mass to 26% by mass, and particularly preferably in the range of 7% by mass to 25% by mass. It is because the said hydrocarbon resin can give the rubber composition excellent in workability and the balance of rolling resistance and wet grip performance because the said content is in the above-mentioned range.
  • the ratio of each of the corresponding compounds may be any ratio, and is not particularly limited, but preferably contains at least cyclopentene, and has 4 to 6 carbon atoms.
  • the proportion of cyclopentene in the alicyclic monoolefin is more preferably 50% by mass or more.
  • An acyclic monoolefin having 4 to 8 carbon atoms has one aliphatic carbon-carbon unsaturated bond in its molecular structure, and is a chain hydrocarbon compound having 4 to 8 carbon atoms having no ring structure It is.
  • Specific examples of the acyclic monoolefin having 4 to 8 carbon atoms include butenes such as 1-butene, 2-butene and isobutylene (2-methylpropene); 1-pentene, 2-pentene, 2-methyl-1 -Pentenes such as butene, 3-methyl-1-butene, 2-methyl-2-butene; hexenes such as 1-hexene, 2-hexene, 2-methyl-1-pentene; 1-heptene, 2-heptene Heptenes such as 2-methyl-1-hexene; 1-octene, 2-octene, 2-methyl-1-heptene, diisobutylene (2,4,4-trimethyl-1-pentene and 2,4,4- Octene
  • the content of the acyclic monoolefin monomer unit having 4 to 8 carbon atoms in the hydrocarbon resin is to provide a rubber composition having excellent workability and excellent balance between rolling resistance and wet grip performance.
  • Any hydrocarbon resin can be used as long as it can be obtained.
  • it can be in the range of 1 to 50% by mass, preferably in the range of 5 to 45% by mass, In particular, it is preferably in the range of 10% by mass to 42% by mass, and particularly preferably in the range of 15% by mass to 40% by mass. It is because the said hydrocarbon resin can give the rubber composition excellent in workability and the balance of rolling resistance and wet grip performance because the said content is in the above-mentioned range.
  • the ratio of each of the corresponding compounds may be any ratio, and is not particularly limited.
  • at least 2-methyl-2-butene Preferably, at least one selected from the group consisting of isobutylene and diisobutylene is included, and the total amount of 2-methyl-2-butene, isobutylene and diisobutylene occupies in the alicyclic monoolefin having 4 to 6 carbon atoms
  • the ratio is more preferably 50% by mass or more.
  • the hydrocarbon resin may contain an alicyclic diolefin as a raw material.
  • An alicyclic diolefin is a hydrocarbon compound having two or more aliphatic carbon-carbon unsaturated bonds and a non-aromatic ring structure in its molecular structure.
  • Specific examples of the alicyclic diolefin include multimers of cyclopentadiene such as cyclopentadiene and dicyclopentadiene, and multimers of methylcyclopentadiene and methylcyclopentadiene.
  • the content of the cycloaliphatic diolefin monomer unit in the hydrocarbon resin is a hydrocarbon resin that is excellent in processability and can provide a rubber composition with a good balance of rolling resistance and wet grip performance.
  • Any material can be used as long as it can be obtained.
  • it can be in the range of 0% by mass to 10% by mass, and preferably in the range of 0% by mass to 7% by mass. It is preferably in the range of 5% by mass, and particularly preferably in the range of 0% by mass to 3% by mass. It is because the said hydrocarbon resin can give the rubber composition excellent in workability and the balance of rolling resistance and wet grip performance because the said content is in the above-mentioned range.
  • the above aliphatic monomer units are 1,3-pentadiene monomer units, alicyclic monoolefin monomer units having 4 to 6 carbon atoms, and acyclic monoolefin monomer units having 4 to 8 carbon atoms.
  • Monomer units may be included.
  • Other monomers used for constituting such other monomer units may be compounds having addition polymerizability that can be addition copolymerized with 1,3-pentadiene or the like other than the aforementioned monomers. There is no particular limitation.
  • Examples of the other monomers include carbon numbers other than 1,3-pentadiene such as 1,3-butadiene, 1,2-butadiene, isoprene, 1,3-hexadiene, and 1,4-pentadiene.
  • An unsaturated monoolefin having 7 or more carbon atoms such as cycloheptene; an acyclic monoolefin having 4 to 8 carbon atoms such as ethylene, propylene and nonene.
  • the content of the other monomer units in the hydrocarbon resin in the hydrocarbon resin is not particularly limited as long as the hydrocarbon resin having the predetermined characteristics can be obtained. Usually, it is in the range of 0% by mass to 30% by mass, preferably in the range of 0% by mass to 25% by mass, and more preferably in the range of 0% by mass to 20% by mass. This is because the hydrocarbon resin can provide a rubber composition having excellent processability and a good balance between rolling resistance and wet grip performance.
  • the hydrocarbon resin can provide a rubber composition having excellent workability and excellent balance of rolling resistance and wet grip performance.
  • it can be in the range of 50% by mass to 99.9% by mass, and preferably in the range of 60% by mass to 90% by mass. It is because the said hydrocarbon resin can give the rubber composition excellent in workability and the balance of rolling resistance and wet grip performance because the said content is in the above-mentioned range.
  • the weight average molecular weight (Mw) of the hydrocarbon resin is not particularly limited as long as it is in the range of 700 to 6000, but it is particularly preferable to be in the range of 900 to 5000. More preferably, it is within the range of 1000 to 4000. This is because, when the weight average molecular weight (Mw) is within the above range, the hydrocarbon resin can be excellent in compatibility with the diene rubber. As a result, the hydrocarbon resin can easily reduce the loss coefficient tan ⁇ at 60 ° C. of the cross-linked product of the rubber composition and can be excellent in rolling resistance. In addition, when the weight average molecular weight (Mw) is within the above-described range, the hydrocarbon resin can easily increase the loss coefficient tan ⁇ at 0 ° C. and can have excellent rolling resistance. Because.
  • the number average molecular weight (Mn) of the hydrocarbon resin can be in the range of 400 to 3000, preferably in the range of 450 to 2500, particularly in the range of 500 to 2000. Is more preferable. This is because when the number average molecular weight (Mn) is within the above-mentioned range, the hydrocarbon resin can be excellent in compatibility with the diene rubber. As a result, the hydrocarbon resin can easily reduce the loss coefficient tan ⁇ at 60 ° C. of the cross-linked product of the rubber composition and can be excellent in rolling resistance.
  • the Z average molecular weight (Mz) of the hydrocarbon resin can be in the range of 1500 to 20000, preferably in the range of 1800 to 15000, particularly in the range of 2000 to 10,000. Is more preferable. This is because, when the Z average molecular weight (Mz) is within the above range, the hydrocarbon resin can be excellent in compatibility with the diene rubber. As a result, the hydrocarbon resin can easily reduce the loss coefficient tan ⁇ at 60 ° C. of the cross-linked product of the rubber composition and can be excellent in rolling resistance.
  • the number average molecular weight (Mn), the weight average molecular weight (Mw), and the Z average molecular weight (Mz) of the hydrocarbon resin are determined as polystyrene-converted values measured by high performance liquid chromatography.
  • Mn number average molecular weight
  • Mw weight average molecular weight
  • Mz Z average molecular weight of the hydrocarbon resin
  • the ratio (Mw / Mn) of the weight average molecular weight to the number average molecular weight of the hydrocarbon resin can be in the range of 1.0 to 4.0, and more preferably in the range of 1.1 to 3.5. In particular, it is more preferable to be in the range of 1.2 to 3.0. This is because when the ratio is within the above-described range, the hydrocarbon resin can be excellent in compatibility with the diene rubber. As a result, the hydrocarbon resin can easily reduce the loss coefficient tan ⁇ at 60 ° C. of the cross-linked product of the rubber composition and can be excellent in wet grip performance.
  • the ratio of the Z average molecular weight to the weight average molecular weight of the hydrocarbon resin can be in the range of 1.0 to 4.0, and in particular, in the range of 1.1 to 3.5. In particular, it is more preferable to be in the range of 1.2 to 3.0. This is because when the ratio is within the above-described range, the hydrocarbon resin can be excellent in compatibility with the diene rubber. As a result, the hydrocarbon resin can easily reduce the loss coefficient tan ⁇ at 60 ° C. of the cross-linked product of the rubber composition and can be excellent in wet grip performance.
  • the softening point of the hydrocarbon resin is not particularly limited as long as it is in the range of 80 ° C. to 150 ° C. Among them, it is preferably in the range of 85 ° C. to 145 ° C., particularly 90 ° C. to More preferably, it is within the range of 140 ° C. This is because when the softening point is within the above-described range, the hydrocarbon resin can be excellent in compatibility with the diene rubber. As a result, the hydrocarbon resin can easily reduce the loss coefficient tan ⁇ at 60 ° C. of the cross-linked product of the rubber composition and can be excellent in rolling resistance. Further, since the softening point is within the above-described range, the hydrocarbon resin can easily increase the loss coefficient tan ⁇ at 0 ° C. and can have excellent wet grip performance. .
  • the softening point in the present invention is a value measured according to JIS K 6863 for hydrocarbon resins, for example.
  • the mixed aniline point (MMAP) of the hydrocarbon resin can be in the range of 25 ° C. to 100 ° C., preferably 27 ° C. to 90 ° C., particularly 30 ° C. to 75 ° C. It is more preferable to be within the range. This is because when the mixed aniline point is within the above range, the hydrocarbon resin can be excellent in compatibility with the diene rubber. As a result, the hydrocarbon resin can easily reduce the loss coefficient tan ⁇ at 60 ° C. of the cross-linked product of the rubber composition and can be excellent in rolling resistance. In addition, since the mixed aniline point is within the above range, the hydrocarbon resin can easily increase the loss coefficient tan ⁇ at 0 ° C. and can have excellent wet grip performance. is there.
  • the mixed aniline point in the present invention is a temperature measured as the lowest temperature at which a mixed solution (volume ratio 2: 1: 1) of aniline, methylcyclohexane and the above hydrocarbon resin exists as a uniform solution. It is a value measured using methylcyclohexane instead of heptane according to JIS K 2256 for hydrocarbon resins.
  • the blending amount of the hydrocarbon resin is not particularly limited as long as it is 1 to 30 parts by mass with respect to 100 parts by mass of the diene rubber. It is preferably within the range of 20 to 20 parts by mass. This is because, when the blending amount is within the above-described range, the rubber composition has excellent processability and excellent balance between rolling resistance and wet grip performance.
  • the blending amount of the hydrocarbon resin is preferably in the range of 1% by mass to 30% by mass of the blending amount of silica, and in particular, in the range of 3% by mass to 25% by mass. .
  • the method for producing the hydrocarbon resin may be any method that can obtain a hydrocarbon resin containing an aliphatic monomer unit and an aromatic monomer unit.
  • a preferred example is a method in which a polymerizable component (monomer mixture A) having monomers capable of constituting a monomer unit and an aromatic monomer unit is subjected to addition polymerization.
  • a hydrocarbon resin can be obtained by addition polymerization using a Friedel-Crafts type cationic polymerization catalyst.
  • a method suitably used for producing the hydrocarbon resin the following aluminum halide (A), halogenated hydrocarbon (B1) in which a halogen atom is bonded to a tertiary carbon atom, and carbon-carbon non-carbon are described.
  • a polymerization catalyst is obtained, and the above aliphatic monomer and The method which has the superposition
  • the addition amount of each monomer contained in the monomer mixture A can be the same as the content of each monomer unit in the hydrocarbon resin.
  • aluminum halide (A) examples include aluminum chloride (AlCl 3 ) and aluminum bromide (AlBr 3 ). Of these, aluminum chloride is preferably used from the viewpoint of versatility.
  • the amount of aluminum halide (A) used is not particularly limited, but is preferably in the range of 0.05 to 10 parts by mass, more preferably 100 parts by mass of the polymerizable component (monomer mixture A). It is within the range of 0.1 to 5 parts by mass.
  • the activity of the polymerization catalyst becomes extremely good.
  • halogenated hydrocarbon (B1) in which a halogen atom is bonded to a tertiary carbon atom include t-butyl chloride, t-butyl bromide, 2-chloro-2-methylbutane, and triphenylmethyl chloride. .
  • t-butyl chloride is particularly preferably used because it has an excellent balance between activity and ease of handling.
  • Examples of the unsaturated bond in the halogenated hydrocarbon (B2) in which a halogen atom is bonded to a carbon atom adjacent to the carbon-carbon unsaturated bond include a carbon-carbon double bond and a carbon-carbon triple bond, and an aromatic ring It also includes a carbon-carbon conjugated double bond in Specific examples of such compounds include benzyl chloride, benzyl bromide, (1-chloroethyl) benzene, allyl chloride, 3-chloro-1-propyne, 3-chloro-1-butene, 3-chloro-1-butyne, Examples include cinnamon chloride. Among these, benzyl chloride is preferably used because it is excellent in balance between activity and ease of handling.
  • halogenated hydrocarbon (B) may be used by 1 type, or may be used in combination of 2 or more types.
  • the amount of the halogenated hydrocarbon (B) used is preferably in the range of 0.05 to 50, more preferably in the range of 0.1 to 10, in terms of the molar ratio to the aluminum halide (A).
  • the order of adding each component of the monomer mixture and the polymerization catalyst to the polymerization reactor is not particularly limited, and may be added in any order, but the polymerization reaction is well controlled, From the viewpoint of more accurately controlling the weight average molecular weight and the like, after adding the monomer mixture and a part of the components of the polymerization catalyst to the polymerization reactor and starting the polymerization reaction, the remainder of the polymerization catalyst is subjected to the polymerization reaction It is preferable to add to the vessel.
  • the aluminum halide (A) and the alicyclic monoolefin may be mixed. preferable. This is because by subjecting the aluminum halide (A) and the alicyclic monoolefin to contact treatment, gel formation can be prevented and a hydrocarbon resin in which the weight average molecular weight and the like are controlled with high accuracy can be obtained.
  • the amount of the alicyclic monoolefin mixed with the aluminum halide (A) is preferably at least 5 times (mass ratio) the amount of the aluminum halide (A). If the amount of the alicyclic monoolefin is too small, the effect of preventing gel formation may be insufficient.
  • the mass ratio of alicyclic monoolefin to aluminum halide (A) is preferably 5: 1 to 120: 1, more preferably 10: 1 to 100: 1, and even more preferably 15: 1 to 80: 1. . If the alicyclic monoolefin is used in an excessive amount from this ratio, the catalytic activity is lowered and the polymerization may not proceed sufficiently.
  • the charging order is not particularly limited, and the aluminum halide (A) may be charged into the alicyclic monoolefin, and conversely, An alicyclic monoolefin may be introduced into the aluminum halide (A). Since mixing usually involves exotherm, an appropriate diluent can also be used. As the diluent, a solvent described later can be used.
  • the aliphatic monomer unit includes a 1,3-pentadiene monomer unit, an acyclic monoolefin monomer unit, etc. in addition to the alicyclic monoolefin monomer unit, as described above.
  • the mixture M of the aluminum halide (A) and the alicyclic monoolefin it is preferable to mix the mixture M with the mixture a containing at least 1,3-pentadiene and the acyclic monoolefin.
  • the mixture a may contain an alicyclic diolefin.
  • the preparation method of the mixture a is not particularly limited, and each of the pure compounds may be mixed to obtain the target mixture a.
  • a mixture containing the target monomer derived from a fraction of a naphtha decomposition product May be used to obtain the desired mixture a.
  • the C5 fraction after extraction of isoprene and cyclopentadiene (including its multimer) can be preferably used.
  • the type of the solvent is not particularly limited as long as it does not inhibit the polymerization reaction, but saturated aliphatic hydrocarbons or aromatic hydrocarbons are preferable.
  • saturated aliphatic hydrocarbon used as the solvent include n-pentane, n-hexane, 2-methylpentane, 3-methylpentane, n-heptane, 2-methylhexane, 3-methylhexane, and 3-ethylpentane.
  • Examples include 5-10 chain saturated aliphatic hydrocarbons; cyclic saturated aliphatic hydrocarbons having 5 to 10 carbon atoms such as cyclopentane, cyclohexane, cycloheptane, cyclooctane and the like.
  • aromatic hydrocarbon used as the solvent include aromatic hydrocarbons having 6 to 10 carbon atoms such as benzene, toluene and xylene.
  • a solvent may be used individually by 1 type and may be used as a 2 or more types of mixed solvent.
  • the amount of the solvent used is not particularly limited, but is preferably in the range of 10 parts by weight to 1,000 parts by weight with respect to 100 parts by weight of the polymerizable component (monomer mixture A), and 50 parts by weight to More preferably, it is in the range of 500 parts by weight.
  • a mixture of an addition polymerizable component and a non-addition polymerizable component such as a mixture of cyclopentane and cyclopentene derived from the C5 fraction is added to the polymerization reaction system, and the addition polymerizable component is a single amount. It can be used as a component of the body mixture, and the non-addition polymerizable component can be used as a solvent.
  • the polymerization temperature for carrying out the polymerization reaction is not particularly limited, but is preferably in the range of ⁇ 20 ° C. to 100 ° C., and preferably in the range of 0 ° C. to 75 ° C. If the polymerization temperature is too low, the polymerization activity may be reduced and productivity may be inferior. If the polymerization temperature is too high, the controllability such as the weight average molecular weight of the resulting hydrocarbon resin may be inferior.
  • the pressure for performing the polymerization reaction may be atmospheric pressure or increased pressure.
  • the polymerization reaction time can be appropriately selected, but is usually selected within the range of 10 minutes to 12 hours, preferably 30 minutes to 6 hours.
  • the polymerization reaction can be stopped by adding a polymerization terminator such as methanol, an aqueous sodium hydroxide solution or an aqueous ammonia solution to the polymerization reaction system when a desired polymerization conversion rate is obtained.
  • a polymerization terminator such as methanol, an aqueous sodium hydroxide solution or an aqueous ammonia solution
  • the method for producing the hydrocarbon resin has at least the polymerization step, but may have other steps as necessary.
  • the other steps include, for example, a catalyst residue that is generated when a polymerization terminator is added in the polymerization step after the polymerization step to inactivate the polymerization catalyst, and the catalyst residue insoluble in the solvent is removed by filtration or the like.
  • the unreacted monomer and solvent are removed, and further, the low molecular weight oligomer component is removed by steam distillation or the like, and the solid resin is obtained by cooling. Etc.
  • diene rubber any diene rubber that can be blended with the hydrocarbon resin and silica in the rubber composition can be used.
  • a diene rubber for example, a diene rubber described in JP-A-2015-189873 can be used. More specifically, the diene rubbers are natural rubber (NR), isoprene rubber (IR), butadiene rubber (BR), styrene-butadiene copolymer rubber (SBR), acrylonitrile-butadiene copolymer rubber (NBR). ), Ethylene-propylene-diene terpolymer (EPDM) and the like.
  • NR natural rubber
  • IR isoprene rubber
  • BR butadiene rubber
  • SBR styrene-butadiene copolymer rubber
  • NBR acrylonitrile-butadiene copolymer rubber
  • EPDM Ethylene-propylene-diene terpolymer
  • styrene-butadiene copolymer rubber natural rubber and the like are preferable. This is because by using the diene rubber, it is possible to obtain a rubber composition having excellent workability and a good balance between rolling resistance and wet grip performance.
  • the diene rubber need only contain at least one kind, and may contain only one kind, or a mixture of two or more kinds.
  • the molecular weight and microstructure of the diene rubber are not particularly limited, and may be terminally modified with an amine, amide, silyl, alkoxysilyl, carboxyl, hydroxyl group or the like, or epoxidized.
  • the diene rubber may be hydrogenated, but is preferably not hydrogenated.
  • silica is blended in the rubber composition together with the diene rubber and the hydrocarbon resin.
  • silica when blended in a rubber composition together with a diene rubber and the above hydrocarbon resin, a rubber composition having excellent processability and excellent balance of rolling resistance and wet grip performance is obtained.
  • the same silica as described in JP-A-2016-3274 can be used. More specifically, the silica may be dry silica, wet silica, colloidal silica, precipitated silica, or the like. In addition, the above types of silica may be used alone or in combination of two or more.
  • the BET specific surface area (measured in accordance with ISO 5794/1) of the silica can be in the range of 100 m 2 / g to 400 m 2 / g, in particular in the range of 150 m 2 / g to 350 m 2 / g. It is preferable to be within.
  • the amount of the silica is not particularly limited as long as it is 80 to 200 parts by mass with respect to 100 parts by mass of the diene rubber, and in particular, 90 parts by mass with respect to 100 parts by mass of the diene rubber. It is preferably in the range of ⁇ 150 parts by mass. This is because, when the blending amount is within the above-described range, the rubber composition has excellent processability and excellent balance between rolling resistance and wet grip performance.
  • the rubber composition of the present invention contains a diene rubber, a hydrocarbon resin, and silica, but may contain other components as necessary.
  • the other components include compounding agents such as a silane coupling agent, a crosslinking agent, a crosslinking accelerator, a crosslinking activator, an anti-aging agent, an activator, a process oil, a plasticizer, a lubricant, and a tackifier. Necessary amount can be blended.
  • Such other components and their contents can be the same as those described in JP-A-2016-30795, for example.
  • the above-mentioned other components can contain fillers other than silica.
  • the filler other than silica those generally used for rubber compositions can be used, for example, carbon black, clay, diatomaceous earth, talc, barium sulfate, calcium carbonate, magnesium carbonate, metal oxide, mica.
  • a filler etc. can be mentioned.
  • carbon black and the like described in JP-A-2016-30795 can be used.
  • the filler is preferably carbon black or the like. This is because the rubber composition is excellent in wet grip properties by being the filler.
  • the filler only needs to contain at least one type, and may contain only one type, or a mixture of two or more types.
  • the filler content other than silica is not particularly limited as long as it is excellent in processability and can provide a rubber composition excellent in the balance between rolling resistance and wet grip performance.
  • the said content can be 120 mass parts or less by the ratio with respect to 100 mass parts of diene rubbers, for example.
  • the rubber composition of the present invention may be prepared by kneading each component according to a conventional method.
  • a component excluding a thermally unstable component such as a crosslinking agent or a crosslinking accelerator and a diene rubber are used.
  • a heat-unstable component such as a crosslinking agent or a crosslinking accelerator can be mixed with the kneaded product to obtain a desired composition.
  • the kneading temperature of the component excluding the thermally unstable component and the diene rubber is preferably in the range of 80 ° C. to 200 ° C., more preferably in the range of 120 ° C.
  • the kneaded product and the thermally unstable component are usually mixed after cooling to 100 ° C. or lower, preferably 80 ° C. or lower.
  • a known crosslinking method can be used.
  • a molding machine corresponding to a desired shape such as an extruder, an injection molding machine, a compressor
  • Examples of the method include forming by a roll or the like, performing a crosslinking reaction by heating, and fixing the shape as a crosslinked product.
  • the molding temperature is usually in the range of 10 ° C to 200 ° C, preferably in the range of 25 ° C to 120 ° C.
  • the crosslinking temperature is usually in the range of 100 ° C.
  • the crosslinking time is usually in the range of 1 minute to 24 hours, preferably 2 minutes to 12 hours. And particularly preferably within the range of 3 minutes to 6 hours.
  • the rubber cross-linked product even if the surface is cross-linked, it may not be sufficiently cross-linked to the inside. Good.
  • the heating method a general method used for crosslinking of the rubber composition such as press heating, steam heating, oven heating, hot air heating, etc. may be appropriately selected.
  • the rubber composition of the present invention has an excellent balance between rolling resistance and wet grip performance.
  • the rubber composition of the present invention is preferably used as a material for each part of the tire such as a tread (cap tread, base tread), carcass, sidewall, bead portion, etc. of the tire, taking advantage of such characteristics.
  • a tread cap tread, base tread
  • tire parts such as treads, carcass, sidewalls, and bead portions, and particularly excellent in low heat generation. Therefore, it can be particularly suitably used as a tread for a fuel-efficient tire, and in particular, it is preferably used for a cap tread.
  • the pneumatic tire of the present invention is characterized by using the above rubber composition in a tread.
  • the tread is one that uses the above rubber composition, that is, one that is formed using the rubber composition, and usually contains a cross-linked product of the rubber composition.
  • the pneumatic tire only needs to have a tread formed using the rubber composition, and other parts may also be formed using the rubber composition.
  • the tread formed using the rubber composition may be a part of the tread or the entire tread, but preferably includes at least a cap tread.
  • the present invention is not limited to the above embodiment.
  • the above-described embodiment is an exemplification, and the present invention has substantially the same configuration as the technical idea described in the claims of the present invention, and any device that exhibits the same function and effect is the present invention. It is included in the technical scope of the invention.
  • the hydrocarbon resin used as a sample is subjected to gel permeation chromatography analysis to determine the number average molecular weight (Mn), weight average molecular weight (Mw) and Z average molecular weight (Mz) in terms of standard polystyrene, and the molecular weight distribution is Mw / Mn ratio and Mz / Mw ratio.
  • the gel permeation chromatography analysis uses “HLC-8320GPC” manufactured by Tosoh Corporation as a measuring device, and the column uses three connected “TSKgel SuperMultipore HZ” manufactured by Tosoh Corporation, with tetrahydrofuran as a solvent. , 40 ° C. and a flow rate of 1.0 mL / min.
  • Measurement item Dynamic storage elastic modulus E ' : Dynamic loss modulus E '' : Loss tangent tan ⁇ -Sample preparation method: punching from sheet-Specimen shape: length 50 mm x width 2 mm x thickness 2 mm ⁇ Number of specimens: 1 ⁇ Distance between clamps: 20mm
  • the obtained polymer solution was charged into a distillation kettle and heated in a nitrogen atmosphere to remove the polymerization solvent and unreacted monomers. Subsequently, the low molecular weight oligomer component was distilled off at 240 ° C. or higher while blowing saturated water vapor, and the hydrocarbon resin of Production Example 1 was obtained.
  • the number average molecular weight, weight average molecular weight, Z average molecular weight, molecular weight distribution, softening point, and mixed aniline point were measured. These measurement results are summarized in Table 1 below.
  • the aromatic monoolefins contained in the mixture a 1 are to be included as aromatic monomer.
  • aromatic monoolefin 0.95 part of styrene (5.0% by mass in the aromatic monomer) and 18.05 parts of 1-vinylnaphthalene (95.0% by mass in the aromatic monomer) were used. Using.
  • styrene is used as an aromatic monomer other than the monomer having a structure in which two or more cyclic structures are bonded, as in Production Example 1.
  • an aromatic monomer is not included.
  • Example 1 Oil-extended emulsion-polymerized styrene butadiene rubber (E-SBR) (trade name “Nipol 1739”, manufactured by Nippon Zeon Co., Ltd., bound styrene content: 40%, vinyl bond content in butadiene unit: 13.
  • E-SBR Oil-extended emulsion-polymerized styrene butadiene rubber
  • the obtained kneaded product was cooled to room temperature and then kneaded again (secondary kneading) at 90 ° C. for 2 minutes in a Banbury mixer, and then the kneaded product was discharged from the mixer.
  • the temperature of the kneaded product at the end of kneading was 145 ° C.
  • the obtained kneaded product was mixed with 1.7 parts of sulfur and a vulcanization accelerator: N-cyclohexyl-2-benzothiazolylsulfenamide (CBS trade name “NOXELLA CZ-G”).
  • CBS trade name “NOXELLA CZ-G” N-cyclohexyl-2-benzothiazolylsulfenamide
  • DPG product name Noxeller D
  • Ouchi Shinsei Chemical Co., Ltd. Diphenylguanidine
  • the kneading conditions for primary kneading, secondary kneading and vulcanizing agent kneading were as shown below.
  • Examples 2 to 3 and Comparative Examples 1 to 3 As shown in Table 2 below, a rubber composition was obtained in the same manner as in Example 1 except that the hydrocarbon resin obtained in Production Examples 2 to 6 was used instead of the hydrocarbon resin obtained in Production Example 1. .
  • the rubber composition is excellent in both rolling resistance and wet grip performance. It was confirmed that Moreover, even when the said rubber composition contains a silica, it has confirmed that the dispersibility of a silica was favorable and became the thing excellent in workability.
  • those having a predetermined proportion of monomer units having a structure in which two or more cyclic structures are bonded, and having characteristics such as a predetermined weight average molecular weight (Mw) and softening point In particular, for example, a hydrocarbon resin having a moderately low weight average molecular weight (Mw) and a ratio (Mw / Mn) of the weight average molecular weight to the number average molecular weight (Mn) and a moderately high softening point, together with silica, is a diene rubber. It was confirmed that the rubber composition was excellent in processability and excellent in both rolling resistance and wet grip performance by containing a predetermined amount.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Tires In General (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

L'invention a pour objet de fournir une composition de caoutchouc qui présente une excellente usinabilité, et un excellent équilibre entre résistance au roulement et performance d'adhérence sur sol mouillé. Plus précisément, l'invention concerne une composition de caoutchouc qui est constituée par mélange de 1 à 30 parties en masse d'une résine hydrocarbure, et de 80 à 200 parties en masse d'une silice, pour 100 parties en masse d'un caoutchouc diénique. Cette composition de caoutchouc est caractéristique en ce que ladite résine hydrocarbure contient une unité monomère aliphatique et une unité monomère aromatique. La teneur, dans ladite unité monomère aromatique, en unité monomère possédant une structure à laquelle sont liées deux structures cycliques ou plus de ladite unité monomère aromatique, est supérieure ou égale à 50% en masse. La masse moléculaire moyenne en poids (Mw) de la composition de caoutchouc est comprise dans une plage de 700 à 6000, et son point de ramollissement est compris dans une plage de 80 à 150°C.
PCT/JP2017/042902 2016-12-01 2017-11-29 Composition de caoutchouc, et pneumatique Ceased WO2018101361A1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2018554211A JP7081495B2 (ja) 2016-12-01 2017-11-29 ゴム組成物および空気入りタイヤ

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2016-234061 2016-12-01
JP2016234061 2016-12-01

Publications (1)

Publication Number Publication Date
WO2018101361A1 true WO2018101361A1 (fr) 2018-06-07

Family

ID=62241661

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2017/042902 Ceased WO2018101361A1 (fr) 2016-12-01 2017-11-29 Composition de caoutchouc, et pneumatique

Country Status (3)

Country Link
JP (1) JP7081495B2 (fr)
TW (1) TW201825578A (fr)
WO (1) WO2018101361A1 (fr)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2020070329A (ja) * 2018-10-30 2020-05-07 日本ゼオン株式会社 ゴム組成物およびそれを用いた空気入りタイヤ
JP2021063184A (ja) * 2019-10-16 2021-04-22 横浜ゴム株式会社 タイヤ用ゴム組成物およびそれを用いた空気入りタイヤ
JP2021063158A (ja) * 2019-10-11 2021-04-22 横浜ゴム株式会社 タイヤ用ゴム組成物およびそれを用いた空気入りタイヤ
JP2021063174A (ja) * 2019-10-15 2021-04-22 住友ゴム工業株式会社 ベーストレッド用組成物及びタイヤ
JP2021063185A (ja) * 2019-10-16 2021-04-22 横浜ゴム株式会社 タイヤ用ゴム組成物およびそれを用いた空気入りタイヤ
JP2021066762A (ja) * 2019-10-18 2021-04-30 横浜ゴム株式会社 タイヤ用ゴム組成物およびそれを用いた空気入りタイヤ

Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0649282A (ja) * 1992-07-30 1994-02-22 Kanegafuchi Chem Ind Co Ltd 熱可塑性樹脂組成物
JP2009019154A (ja) * 2007-07-13 2009-01-29 Sumitomo Rubber Ind Ltd タイヤ用ゴム組成物
WO2013115010A1 (fr) * 2012-02-01 2013-08-08 住友ゴム工業株式会社 Copolymère de diène conjugué ramifié, composition de caoutchouc et pneumatique
WO2013132905A1 (fr) * 2012-03-06 2013-09-12 住友ゴム工業株式会社 Copolymère diène conjugué ramifié hydrogéné, composition de caoutchouc et pneumatique
US20140044918A1 (en) * 2012-08-09 2014-02-13 Guangdong Shengyi Sci.Tech Co., Ltd Polyphenylene ether resin composition, and a prepreg and a copper clad laminate made therefrom
JP2014088544A (ja) * 2012-10-04 2014-05-15 Sumitomo Rubber Ind Ltd 分枝共役ジエン共重合体、ゴム組成物および空気入りタイヤ
JP2014224196A (ja) * 2013-05-16 2014-12-04 住友ゴム工業株式会社 分枝共役ジエン共重合体および水添分枝共役ジエン共重合体、ゴム組成物、並びに空気入りタイヤ
JP2015007194A (ja) * 2013-06-25 2015-01-15 住友ゴム工業株式会社 タイヤ用ゴム組成物およびタイヤ
JP2015086315A (ja) * 2013-10-31 2015-05-07 住友ゴム工業株式会社 ゴム組成物および空気入りタイヤ
JP2016512183A (ja) * 2013-03-05 2016-04-25 カンパニー ジェネラレ デ エスタブリシュメンツ ミシュラン タイヤ用の多層ラミネート

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0088510B1 (fr) * 1982-02-15 1988-03-09 Exxon Research And Engineering Company Résines de pétrole
US4558107A (en) * 1982-06-11 1985-12-10 Exxon Research & Engineering Co. Aromatic high softening point petroleum resins and process for its preparation
JP3464504B2 (ja) * 1993-07-23 2003-11-10 新日本石油化学株式会社 印刷インキ用石油樹脂組成物およびその製造法
JP4765141B2 (ja) 2000-05-19 2011-09-07 東ソー株式会社 芳香族系炭化水素樹脂及びそれよりなるホットメルト接着用芳香族系炭化水素樹脂組成物
JP2006206850A (ja) 2005-01-31 2006-08-10 Nippon Zeon Co Ltd 変性石油樹脂及びそれを用いた粘着剤組成物
JP2008274120A (ja) 2007-04-27 2008-11-13 Sumitomo Rubber Ind Ltd ゴム組成物およびそれを用いたタイヤ
JP2008274121A (ja) 2007-04-27 2008-11-13 Sumitomo Rubber Ind Ltd ゴム組成物およびそれを用いたタイヤ
US8697793B2 (en) 2010-03-19 2014-04-15 The Yokohama Rubber Co., Ltd. Rubber composition for use in tires
JP2012251118A (ja) 2011-06-07 2012-12-20 Jsr Corp 共役ジエン系エラストマーおよびその製造方法並びにゴム組成物、ゴム弾性体およびタイヤ
CN102757530B (zh) 2012-06-27 2014-01-29 宁波职业技术学院 一种浅色冷聚碳九石油树脂的制备方法

Patent Citations (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0649282A (ja) * 1992-07-30 1994-02-22 Kanegafuchi Chem Ind Co Ltd 熱可塑性樹脂組成物
JP2009019154A (ja) * 2007-07-13 2009-01-29 Sumitomo Rubber Ind Ltd タイヤ用ゴム組成物
WO2013115010A1 (fr) * 2012-02-01 2013-08-08 住友ゴム工業株式会社 Copolymère de diène conjugué ramifié, composition de caoutchouc et pneumatique
WO2013132905A1 (fr) * 2012-03-06 2013-09-12 住友ゴム工業株式会社 Copolymère diène conjugué ramifié hydrogéné, composition de caoutchouc et pneumatique
US20140044918A1 (en) * 2012-08-09 2014-02-13 Guangdong Shengyi Sci.Tech Co., Ltd Polyphenylene ether resin composition, and a prepreg and a copper clad laminate made therefrom
JP2014088544A (ja) * 2012-10-04 2014-05-15 Sumitomo Rubber Ind Ltd 分枝共役ジエン共重合体、ゴム組成物および空気入りタイヤ
JP2016512183A (ja) * 2013-03-05 2016-04-25 カンパニー ジェネラレ デ エスタブリシュメンツ ミシュラン タイヤ用の多層ラミネート
JP2014224196A (ja) * 2013-05-16 2014-12-04 住友ゴム工業株式会社 分枝共役ジエン共重合体および水添分枝共役ジエン共重合体、ゴム組成物、並びに空気入りタイヤ
JP2015007194A (ja) * 2013-06-25 2015-01-15 住友ゴム工業株式会社 タイヤ用ゴム組成物およびタイヤ
JP2015086315A (ja) * 2013-10-31 2015-05-07 住友ゴム工業株式会社 ゴム組成物および空気入りタイヤ

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2020070329A (ja) * 2018-10-30 2020-05-07 日本ゼオン株式会社 ゴム組成物およびそれを用いた空気入りタイヤ
JP7255136B2 (ja) 2018-10-30 2023-04-11 日本ゼオン株式会社 ゴム組成物およびそれを用いた空気入りタイヤ
JP2021063158A (ja) * 2019-10-11 2021-04-22 横浜ゴム株式会社 タイヤ用ゴム組成物およびそれを用いた空気入りタイヤ
JP7397291B2 (ja) 2019-10-11 2023-12-13 横浜ゴム株式会社 タイヤ用ゴム組成物およびそれを用いた空気入りタイヤ
JP2021063174A (ja) * 2019-10-15 2021-04-22 住友ゴム工業株式会社 ベーストレッド用組成物及びタイヤ
JP7338391B2 (ja) 2019-10-15 2023-09-05 住友ゴム工業株式会社 ベーストレッド用組成物及びタイヤ
JP2021063184A (ja) * 2019-10-16 2021-04-22 横浜ゴム株式会社 タイヤ用ゴム組成物およびそれを用いた空気入りタイヤ
JP2021063185A (ja) * 2019-10-16 2021-04-22 横浜ゴム株式会社 タイヤ用ゴム組成物およびそれを用いた空気入りタイヤ
JP7397293B2 (ja) 2019-10-16 2023-12-13 横浜ゴム株式会社 タイヤ用ゴム組成物およびそれを用いた空気入りタイヤ
JP7397292B2 (ja) 2019-10-16 2023-12-13 横浜ゴム株式会社 タイヤ用ゴム組成物およびそれを用いた空気入りタイヤ
JP2021066762A (ja) * 2019-10-18 2021-04-30 横浜ゴム株式会社 タイヤ用ゴム組成物およびそれを用いた空気入りタイヤ
JP7397294B2 (ja) 2019-10-18 2023-12-13 横浜ゴム株式会社 タイヤ用ゴム組成物およびそれを用いた空気入りタイヤ

Also Published As

Publication number Publication date
TW201825578A (zh) 2018-07-16
JP7081495B2 (ja) 2022-06-07
JPWO2018101361A1 (ja) 2019-10-24

Similar Documents

Publication Publication Date Title
JP7081495B2 (ja) ゴム組成物および空気入りタイヤ
JP6729085B2 (ja) 炭化水素樹脂およびタイヤ用エラストマー組成物
JP7255137B2 (ja) ゴム組成物およびそれを用いた空気入りタイヤ
JP7452431B2 (ja) ゴム組成物およびそれを用いた空気入りタイヤ
JP7255136B2 (ja) ゴム組成物およびそれを用いた空気入りタイヤ
JP6954305B2 (ja) ゴム組成物および空気入りタイヤ
JP7081494B2 (ja) ゴム組成物および空気入りタイヤ
JP6780325B2 (ja) 変性炭化水素樹脂およびタイヤ用エラストマー組成物
JP6954304B2 (ja) ゴム組成物および空気入りタイヤ
JP7293892B2 (ja) ゴム組成物
JP6828737B2 (ja) シラン変性炭化水素樹脂およびタイヤ用エラストマー組成物
JP7081496B2 (ja) ゴム組成物および空気入りタイヤ
JP7718271B2 (ja) ゴム組成物ならびにそれを用いたゴム架橋物および空気入りタイヤ
CN117157352A (zh) 橡胶组合物以及使用其的橡胶交联物和充气轮胎
JP6954303B2 (ja) ゴム組成物および空気入りタイヤ
JP2024154452A (ja) ゴム組成物
JP2024067610A (ja) ゴム組成物
WO2024219257A1 (fr) Composition de caoutchouc
JP2024154451A (ja) ゴム組成物

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 17875130

Country of ref document: EP

Kind code of ref document: A1

ENP Entry into the national phase

Ref document number: 2018554211

Country of ref document: JP

Kind code of ref document: A

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 17875130

Country of ref document: EP

Kind code of ref document: A1