CN101230157B - Rubber composition for tire tread and pneumatic tire using the same - Google Patents
Rubber composition for tire tread and pneumatic tire using the same Download PDFInfo
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- CN101230157B CN101230157B CN2008100037208A CN200810003720A CN101230157B CN 101230157 B CN101230157 B CN 101230157B CN 2008100037208 A CN2008100037208 A CN 2008100037208A CN 200810003720 A CN200810003720 A CN 200810003720A CN 101230157 B CN101230157 B CN 101230157B
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- 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
Abstract
The present invention provides a rubber composition for a tire tread, in which processability, abrasion resistance, rolling resistance properties and wet grip performance are improved in a balanced manner. Specifically, the present invention provides a rubber composition for a tire tread comprising 5 to 150 parts by weight of silica having nitrogen-adsorbing specific surface area of 100 to 300 m<2>/g based on 100 parts of a rubber component containing 5 to 100% by weight of an epoxidized natural rubber, and 1 to 20 parts by weight of a silane coupling agent and 0.1 to 20 parts by weight of ananionic surfactant based on 100 parts by weight of the silica; and a rubber composition for a tire tread comprising 5 to 150 parts by weight of silica having nitrogen-adsorbing specific surface area of 100 to 300 m<2>/g and 1 to 10 parts by weight of a metal salt of stearic acid, based on 100 parts of a rubber component containing 5 to 100% by weight of an epoxidized natural rubber, and 1 to 20 parts by weight of a silane coupling agent based on 100 parts by weight of the silica.
Description
The application is dividing an application of following patent application:
Application number: 200510053946.5
The applying date: on March 10th, 2005
Invention and created name: rubber composition for tire tread and use the pneumatic tyre of this rubber combination
Technical field
The present invention relates to a kind of rubber composition for tire tread and use the pneumatic tyre of this rubber combination.
Background technology
In recent years, to since the concern that the oil price that oil supply and exhausted problem cause rises increase to some extent.And, from environmental problem for example conservation of resources and guarding rigidly prevent that the Carbon emission regulations from considering that natural resources is just re-recognized.Tire industry is no exception, and as a kind of elastomeric surrogate, natural rubber just is being caused attention.Natural rubber has high mechanical strength and outstanding wear resistance, therefore often is used to for example truck/passenger tyre of outsize tire.Yet, because natural rubber has only low-molecular-weight methyl on side chain, and have lower glass transition temperatures (Tg)-60 ℃, so the relatively poor problem of anti-skid is arranged.And because natural rubber is a kind of natural resources, its ozone resistants, resistance to heat aging and weathering resistance are relatively poor.
For addressing the above problem, can use natural rubber derivative for example cyclized hatural rubber, chlorinated natural rubber and epoxy natural rubber.For example, JP-A-6-220254, JP-A-7-90123, JP-A-7-149955 and JP-A-2001-233995 provide the method for epoxy natural rubber as tire material of using.Here, epoxy natural rubber refers to wherein unsaturated double-bond by epoxidized natural rubber.Epoxy natural rubber has the second-order transition temperature higher than natural rubber (Tg), and has outstanding physical strength, wear resistance and ventilation property, and this is owing to make the event of force of cohesion increase of molecule as the epoxy group(ing) of polar group.Concrete, the silicon-dioxide that in rubber combination, comprises, the silanol group of silica sphere and the epoxy group(ing) of epoxy natural rubber have been understood can interact, and as a result of, the physical strength of its acquisition is identical with adding sooty composition with wear resistance.
Yet, though epoxy natural rubber has very big hysteresis loss and outstanding wet anti-skid, even if when containing silicon-dioxide, there is rolling resistance to increase the situation of (rolling resistance degradation).In addition, because the interaction of epoxy natural rubber and silicon-dioxide is very strong, at epoxy natural rubber and other elastoprenes mutually in the blended compound, the silicon-dioxide tendency is present in the epoxy natural rubber part, so as a result of, just problem occurred, not only processing characteristics descends, and hardness increase, and wear resistance and resistance to heat aging decline.
JP-A-11-71479 has described the method for mixing specific stearic aeic derivative.By using specific stearic aeic derivative as for the rubber components processing aid of natural rubber and synthetic polyisoprene for example, rubber is softened and the dispersiveness of silicon-dioxide and other Synergist S-421 95s becomes better.As a result of, processing characteristics and wear resistance are improved.Yet epoxy natural rubber is not used as rubber components in this method, and processing characteristics and wear resistance are also undesirable.
Summary of the invention
The object of the invention is to provide a kind of rubber composition for tire tread, and its processing characteristics, wear resistance, rolling resistance performance and wet anti-skid can both be improved with balance mode.
First embodiment of the present invention relates to a kind of rubber composition for tire tread, it comprises: the rubber components that contains the epoxy natural rubber of 5～100wt% with 100 weight parts is a benchmark, the silicon-dioxide that contains 5～150 weight parts, its nitrogen adsorption specific surface area is 100～300m
2/ g, and be benchmark with the silicon-dioxide of 100 weight parts, the silane coupling agent of 1～20 weight part and the anion surfactant of 0.1～20 weight part contained.
This rubber composition for tire tread is a benchmark with the rubber components of 100 weight parts, preferably comprises the plant extract oil of 1～50 weight part.
Second embodiment of the present invention relates to a kind of rubber composition for tire tread, it comprises: the rubber components that contains the epoxy natural rubber of 5～100wt% with 100 weight parts is a benchmark, the silicon-dioxide that contains 5～150 weight parts, its nitrogen adsorption specific surface area is 100～300m
2The Metallic stearates of/g and 1～10 weight part, and be benchmark with the silicon-dioxide of 100 weight parts, the silane coupling agent of 1～20 weight part contained.
Described Metallic stearates is preferably the alkaline-earth metal metal-salt.
Simultaneously, the invention still further relates to the pneumatic tyre of the rubber composition for tire tread in a kind of the present invention of containing first or second embodiment.
Embodiment
The rubber composition for tire tread of first embodiment of the invention includes: rubber components, silicon-dioxide, silane coupling agent and anion surfactant.
Rubber components comprises epoxy natural rubber.As epoxy natural rubber, can use the coml epoxy natural rubber, perhaps will re-use behind the natural rubber epoxidation.The method of epoxy natural rubber does not have particular restriction, and the operable method of epoxidised operation has for example chloroethanol method, direct oxidation method, hydrogen peroxide method, alkylation hydrogen peroxide method and mistake acid system.An example of described method is with natural rubber and for example peracetic acid or peroxyformic acid reaction of organic peracid.
The epoxidation degree of epoxy natural rubber preferably is at least 5mol%, further preferably is at least 10mol%.When the epoxidation degree is lower than 5mol%, the modified effect of rubber combination there is the trend of reducing.And the epoxidation degree preferably is at most 80mol%, further preferably is at most 60mol%.When the epoxidation degree is higher than 80mol%, polymeric constituent meeting gelation, this is disadvantageous.
The content of the epoxy natural rubber in the rubber components is at least 5wt%, preferably is at least 10wt%.When the content of epoxy natural rubber was lower than 5wt%, anti-skid can not get demonstrating fully, and this is disadvantageous.And the content of epoxy natural rubber is at most 100wt%, preferably is at most 95wt%, further preferably is at most 90wt%.
The epoxy natural rubber that the example of rubber components uses, also have natural rubber and/or diene synthetics in rubber composition for tire tread in the first embodiment.
The example of diene synthetics has styrene-butadiene rubber(SBR) (SBR), polybutadiene rubber (BR), polyisoprene rubber (IR), terpolymer EP rubber (EPDM), chloroprene rubber (CR), paracril (NBR), isoprene-isobutylene rubber (IIR) and halogenated butyl rubber.These rubber components can use separately, but also two or more is used in combination.
The example of silicon-dioxide can be the silicon-dioxide of wet method or dried preparation, not special restriction.
Nitrogen adsorption specific surface area (the N of silicon-dioxide
2SA) be at least 100m
2/ g preferably is at least 120m
2/ g.N when silicon-dioxide
2The SA value is lower than 100m
2During/g, the reinforced effects of mixing silicon-dioxide is very little.And, the N of silicon-dioxide
2SA is at most 300m
2/ g preferably is at most 280m
2/ g.N when silicon-dioxide
2The SA value is higher than 300m
2During/g, the dispersity of silicon-dioxide reduces, and the increase of the heat generation of rubber combination, and this is disadvantageous.
Rubber components with 100 weight parts is a benchmark, and the content of silicon-dioxide is at least 5 weight parts, preferably is at least 10 weight parts, further preferably is at least 15 weight parts.When the content of silicon-dioxide was lower than 5 weight parts, low heat generation and wet anti-skid can not demonstrate fully.And the content of silicon-dioxide is at most 150 weight parts, preferably is at most 120 weight parts, further preferably is at most 100 weight parts.When the content of silicon-dioxide during greater than 150 weight parts, processing characteristics and workability variation, this is disadvantageous.
Rubber composition for tire tread among the present invention comprises silane coupling agent.The silane coupling agent that be fit to use among the present invention is any conventional silanes coupling agent that can use together with silica-filled thing.Concrete example is two (3-triethoxysilylpropyltetrasulfide) tetrasulfide, two (2-triethoxysilyl ethyl) tetrasulfide, two (4-triethoxysilyl butyl) tetrasulfide, two (3-trimethoxy-silylpropyl) tetrasulfide, two (2-trimethoxysilylethylgroup group) tetrasulfide, two (4-trimethoxysilyl butyl) tetrasulfide, two (3-methyl diethoxy silyl propyl group) tetrasulfide, two (2-methyl dimethoxy oxygen base silyl ethyl) tetrasulfide, two (4-methyl dimethoxy oxygen base silyl butyl) tetrasulfide, two (3-triethoxysilylpropyltetrasulfide) trisulphide, two (2-triethoxysilyl ethyl) trisulphide, two (4-triethoxysilyl butyl) trisulphide, two (3-trimethoxy-silylpropyl) trisulphide, two (2-trimethoxysilylethylgroup group) trisulphide, two (4-trimethoxysilyl butyl) trisulphide, two (3-triethoxysilylpropyltetrasulfide) disulphide, two (2-triethoxysilyl ethyl) disulphide, two (4-triethoxysilyl butyl) disulphide, two (3-trimethoxy-silylpropyl) disulphide, two (2-trimethoxysilylethylgroup group) disulphide, two (4-trimethoxysilyl butyl) disulphide, two (3-methyl diethoxy silyl propyl group) disulphide, two (2-methyl diethoxy silyl propyl group) disulphide, two (4-methyl diethoxy silyl propyl group) disulphide, two (3-methyl dimethoxy oxygen base silyl butyl) disulphide, two (2-methyl dimethoxy oxygen base silyl propyl group) disulphide, two (4-methyl dimethoxy oxygen base silyl propyl group) disulphide, 3-sulfydryl propyl trimethoxy silicane, 3-sulfydryl propyl-triethoxysilicane, 2-mercaptoethyl Trimethoxy silane, 2-sulfydryl triethyl triethoxyl silane, the 3-aminopropyltriethoxywerene werene, the 3-TSL 8330,3-(2-amino-ethyl) aminopropyltriethoxywerene werene, 3-(2-amino-ethyl) TSL 8330, γ-epoxypropoxy triethoxyl silane, γ-Huan Yangbingyangbingjisanjiayangjiguiwan, γ-epoxypropoxy methyldiethoxysilane and γ-epoxypropoxy methyl dimethoxysilane.Particularly, silane coupling agent preferably satisfies following formula:
(C
nH
2n+1O)
3-Si-(CH
2)
m-S
1-(CH
2)
m-Si-(C
nH
2n+1O)
3
In formula, 1 represents the number of sulphur atom in the polysulphide part, and n is 1～3 integer, and m is 1～4 integer, and 1 mean value is 2.1～3.5.When the mean value when 1 was lower than 2.1, the reactivity of silane coupling agent and rubber components had the trend of variation, and when mean value greater than 3.5 the time, the gelation in can accelerator.
In satisfying the silane coupling agent of following formula, from satisfying effect and the low-cost consideration that adds coupling agent simultaneously, be fit to use two (3-triethoxysilylpropyltetrasulfide) disulphide, two (3-trimethoxy-silylpropyl) disulphide, two (3-methyl diethoxy silyl propyl group) disulphide and two (3-methyl dimethoxy oxygen base silyl propyl group) disulphide.These coupling agents can use separately, but also two or more is used in combination.
Silicon-dioxide with 100 weight parts is benchmark, and the content of silane coupling agent is at least 1 weight part, preferably is at least 2 weight parts.When the content of silane coupling agent was lower than 1 weight part, the dispersity that the effect of adding silane coupling agent for example improves silicon-dioxide can not demonstrate fully.And the content of silane coupling agent is at most 20 weight parts, preferably is at most 15 weight parts.When the content of silane coupling agent during greater than 20 weight parts, coupling effect can not demonstrate fully, although cost is higher and strengthen the property and wear resistance descends, this is disadvantageous.Consider that from dispersion effect and coupling effect the content of silane coupling agent is preferably 2～15 weight parts.
There is no particular restriction for anion surfactant, and can use tradition to be used as the anion surfactant and the pigment of weighting material dispersion agent.Example comprises soap, alkyl-sulphate, alkylbenzene sulfonate, sulfonated alkyl naphathalene, salts of alkyl sulfosuccinates ester, alkyl biphenyl ether stilbene-4,4'-bis-(1-azo-3, 4-dihydroxy-benzene)-2,2'-disulfonate, 2-naphthalenesulfonic acid-formaldehyde condensate and polycarboxylate polymer type tensio-active agent.Wherein, be fit to use 2-naphthalenesulfonic acid-formaldehyde condensate and polycarboxylate polymer type tensio-active agent.
Silicon-dioxide with 100 weight parts is benchmark, and the content of anion surfactant is at least 0.1 weight part, preferably is at least 0.5 weight part.When the content of anion surfactant was lower than 0.1 weight part, consistency can not demonstrate fully.And the content of anion surfactant is at most 20 weight parts, preferably is at most 15 weight parts.When the content of anion surfactant during greater than 20 weight parts, hardness and modulus (modulus) reduce, and strengthen the property and wear resistance descends, and this is disadvantageous.
The rubber composition for tire tread of first embodiment of the invention preferably comprises a kind of plant extract oil as tenderizer.
The example of plant extract oil has Viscotrol C, Oleum Gossypii semen, linseed oil, rapeseed oil, soybean oil, plam oil, Oleum Cocois, peanut oil, Japan tallow, rosin, pine tar, Dipentine, Stockholm tar and Yatall MA.
Normally used tenderizer is the mineral tenderizers in the rubber composition for tire, for example the co-oligomer of process oil, ethene and α-paraffin, Paraffin Wax Semi Refined, whiteruss, white oil, Vaseline, sulfonated petro-leum, rock asphalt, petroleum pitch and petroleum resin.Yet, consider from environmental problem, mineral tenderizer relatively, more preferably plant tenderizer, and, from workability and Effect on Performance degree being considered preferred especially Oleum Gossypii semen, rapeseed oil and soybean oil.
Rubber components with 100 weight parts is a benchmark, and the content of plant extract oil preferably is at least 1 weight part, further preferably is at least 5 weight parts.When the content of plant extract oil is lower than 1 weight part, make rubber plastifying effect that the trend of reducing be arranged.And the content of plant extract oil preferably is at most 50 weight parts, further preferably is at most 45 weight parts.When the content of plant extract oil during greater than 50 weight parts, consistency descends, and poor processability and plant extract oil are oozed out, and this is disadvantageous.
Except rubber components, silicon-dioxide, silane coupling agent, anion surfactant and plant extract oil, the Synergist S-421 95 that rubber industry is commonly used, for example comprise sooty toughener, antioxidant, vulcanizing agent (for example sulphur), vulcanization accelerator and vulcanization accelerator additive, can be mixed in the rubber composition for tire tread of first embodiment of the invention where necessary.
The rubber composition for tire tread of second embodiment of the invention includes: rubber components, silicon-dioxide, Metallic stearates and silane coupling agent.Rubber components, silicon-dioxide and silane coupling agent are employed identical in the rubber composition for tire tread with first embodiment of the invention.
The example of Metallic stearates has Magnesium Stearate, ten dihydroxystearic acid magnesium, calcium stearate, ten dihydroxystearic acid calcium, barium stearate, ten dihydroxystearic acid barium, Zinic stearas and ten dihydroxystearic acid zinc.Wherein,, preferably use the alkaline-earth metal metal-salt from improving heat-resisting effect and considering with the consistency of epoxy natural rubber, and further preferred calcium stearate, ten dihydroxystearic acid calcium, barium stearate and the ten dihydroxystearic acid barium of using.
Rubber components with 100 weight parts is a benchmark, and the content of Metallic stearates is at least 1 weight part, preferably is at least 1.5 weight parts.When the content of Metallic stearates was lower than 1 weight part, consistency and raising heat-resisting effect can not fully manifest.And the content of Metallic stearates is at most 10 weight parts, preferably is at most 8 weight parts.When the content of Metallic stearates during greater than 10 weight parts, hardness and modulus reduce, and wear resistance descends, and this is disadvantageous.
Except rubber components, silicon-dioxide, silane coupling agent and Metallic stearates, the Synergist S-421 95 that rubber industry is commonly used, for example comprise sooty toughener, tenderizer (for example oil), antioxidant, vulcanizing agent (for example sulphur), vulcanization accelerator and vulcanization accelerator additive, can be mixed in the rubber composition for tire tread of second embodiment of the invention where necessary.
Rubber composition for tire of the present invention except rubber components, also preferably comprises: the anion surfactant in silicon-dioxide and silane coupling agent, first embodiment and the mixture of the Metallic stearates in second embodiment.By containing the mixture of said components, its processing characteristics, wear resistance, rolling resistance performance and wet anti-skid can both be improved with balance mode.
And when anion surfactant and Metallic stearates are mixed in the rubber composition for tire of the present invention in the above described manner, the plant extract oil in first embodiment especially preferably is mixed into as tenderizer.
Pneumatic tyre among the present invention is to use the rubber composition for tire tread in the first embodiment of the invention and second embodiment, makes with traditional method.That is,, under sulfided state not, be extruded into each parts of tire, in the tire mold machine, form tire with traditional method then, thereby make unvulcanized tire rubber composition for tire tread of the present invention (adding above-mentioned additive in case of necessity therein).This not vulcanized tyre is made vulcanized tyre after heating and pressurization in vulcanizing apparatus.
Hereinafter, will describe in detail to the present invention by embodiment, but the invention is not restricted to these.
Various chemical used among the embodiment are as described below.
Natural rubber: RSS#3
Epoxy natural rubber: ENR-50 (the epoxidation rate: 50mol%), available from Kumplan Guthrie Berhad (Malaysia)
Styrene-butadiene rubber(SBR): SBR 1502 (styrene content: 23.5wt%), available from JSR company
Silicon-dioxide: Ultrasil VN3 (N
2SA:210m
2/ g), available from Degussa company
Silane coupling agent: Si266 (two (3-triethoxysilylpropyltetrasulfide) disulphide) (1 mean value: 2.2), available from Degussa company
Aromatic oil: JOMO Process X140, available from Japan Energy company
Plant extract oil: refined soybean oil, available from Nisshin Oillio company
Anion surfactant 1:DEMOL EP (special polycarboxylate polymer type tensio-active agent) is available from KAO company
Anion surfactant 2:DEMOL MS (aryl sulfonic acid sodium formaldehyde condenses) is available from KAO company
Calcium stearate: GF200 is available from NOF company
Barium stearate: barium stearate, available from Sakai chemical industry company limited
Antioxidant: NOCRAC 6C (N-(1, the 3-dimethylbutyl)-N '-phenyl-Ursol D) is available from Ouchi Shinko chemical industry company limited
Stearic acid: stearic acid, available from NOF company
Zinc oxide: 1 type zinc oxide, smelt company limited available from the Mitsui mining industry
Sulphur: the sulphur powder, available from Tsurumi chemistry company limited
Vulcanization accelerator TBBS:NoccelerNS (the N-tertiary butyl-2-[4-morpholinodithio sulfinyl amine) is available from Ouchi Shinko chemical industry company limited
Accelerator D PG:Nocceler D (1, the 3-vulkacit D) is available from Ouchi Shinko chemical industry company limited
Embodiment 1～16 and reference examples 1～7
Various chemical are mediated according to composition shown in table 1～5 make each rubbery sample, above-mentioned composition 160 ℃ of following press vulcanizations 20 minutes, is made the sulfuration sample, and this sample is carried out following performance test.
The processing characteristics test
Mooney viscosity is pressed the mooney viscosity testing method of JIS K6300 standard, measures under 130 ℃ of conditions.In table 1 and 5 with reference examples 1 (ML
1+4) mooney viscosity be 100 to make benchmark, in table 2～4 with reference examples 4 (ML
1+4) mooney viscosity be 100 to make benchmark, processing characteristics is represented according to following formula in the mode of coefficient.Coefficient is big more, and mooney viscosity is low more, and then processing characteristics is good more.
(mooney viscosity coefficient)=(ML in the reference examples 1 or 4
1+4ML in each composition of)/(
1+4) * 100
Wearability test
The test of Lamboum abrasion loss is to use Lamboum wear testing device, carries out under 20 ℃, slip ratio 20%, the condition of 5 minutes test durations, and calculates the volumetric wear amount of each composition.Being 100 to make benchmark with the loss of reference examples 1 in table 1 and 5, is 100 to make benchmark with the loss of reference examples 4 in table 2～4, and wear resistance is represented according to following formula in the mode of coefficient.Coefficient is big more, and wear resistance is good more.
(wearing coefficient)=(loss in the reference examples 1 or 4)/(loss in each composition) * 100
The rolling resistance test
Use the tan δ of visco-elasticity photometer VES (manufacturings of Iwamoto company) each composition of mensuration under the condition of 70 ℃, initial stress 10% and dynamic stress 2%.Being 100 to make benchmark with the tan δ of reference examples 1 in table 1 and 5, is 100 to make benchmark with the tan δ of reference examples 4 in table 2～4, and rolling resistance is represented according to following formula in the mode of coefficient.Coefficient is big more, and rolling resistance descends many more, and then the rolling resistance performance is good more.
(coefficient of rolling resistance)=(the tan δ in the reference examples 1 or 4)/(the tan δ in each composition) * 100
Wet anti-skid test
Wet anti-skid is the method according to ASTM E300-83, and the portable slip tstr that uses The Munro Group London Stanley branch office to make is tested.Being 100 to make benchmark with the measured value of reference examples 1 in table 1 and 5, is 100 to make benchmark with the measured value of reference examples 4 in table 2～4, and wet anti-skid is represented according to following formula in the mode of coefficient.Coefficient is big more, and then wet anti-skid is good more.
(wet anti-skid coefficient)=(measured value in each composition)/(measured value in the reference examples 1 or 4) * 100
Measurement result is shown in table 1～5.
Table 1
From the result of table 1 as can be seen, by adding anion surfactant, rolling resistance performance and wet anti-skid are improved under processing characteristics or the undiminished situation of wear resistance.
Table 2
From the result of table 2 as can be seen, by adding Metallic stearates, tensile property, wear resistance and post-heating aging resistance are improved.
Table 3
From the result of table 3 as can be seen, by Metallic stearates being added in the mixture of epoxy natural rubber and natural rubber, wear resistance and rolling resistance performance have obtained remarkable improvement.And the post-heating aging resistance also is improved, and the scope that 100% modulus improves enlarges markedly.
Table 4
From the result of table 4 as can be seen, by Metallic stearates being added in the mixture of epoxy natural rubber and styrene-butadiene rubber(SBR), wear resistance and post-heating aging resistance are improved.
Table 5
From the result of table 5 as can be seen, by in the composition that comprises epoxy natural rubber and silicon-dioxide, adding Metallic stearates and anion surfactant simultaneously, processing characteristics and wear resistance are improved and the not reduction of rolling resistance performance and wet anti-skid, and performance is improved in the equilibrated mode.
According to first embodiment of the invention, by adding epoxy natural rubber, silicon-dioxide, silane coupling agent and anion surfactant, make a kind of rubber composition for tire tread, its rolling resistance performance and wet anti-skid are improved and the not reduction of processing characteristics and wear resistance.
And, according to second embodiment of the invention, by adding epoxy natural rubber, silicon-dioxide, silane coupling agent and Metallic stearates, make a kind of rubber composition for tire tread, its wear resistance and thermotolerance are improved and the not reduction of rolling resistance performance and wet anti-skid.
In addition, according to the present invention, by adding the mixture of anion surfactant and a kind of Metallic stearates, itself and epoxy natural rubber, silicon-dioxide and silane coupling agent are mixed together, make a kind of rubber composition for tire tread, its processing characteristics, wear resistance, rolling resistance performance and wet anti-skid can both be improved with balance mode.
Claims (3)
1. rubber composition for tire tread, it comprises:
The rubber components that contains the epoxy natural rubber of 5～100wt% with 100 weight parts is a benchmark, and the nitrogen adsorption specific surface area of 5～150 weight parts is 100～300m
2The silicon-dioxide of/g, and
With the described silicon-dioxide of 100 weight parts is benchmark, the anion surfactant of 1～20 weight part silane coupling agent and 0.1～20 weight part,
Wherein, described anion surfactant is as the dispersion agent of described silicon-dioxide, and described anion surfactant is alkyl-sulphate, alkylbenzene sulfonate, sulfonated alkyl naphathalene, salts of alkyl sulfosuccinates ester, alkyl biphenyl ether stilbene-4,4'-bis-(1-azo-3, 4-dihydroxy-benzene)-2,2'-disulfonate, 2-naphthalenesulfonic acid-formaldehyde condensate or polycarboxylate polymer type tensio-active agent.
2. rubber composition for tire tread as claimed in claim 1 is characterized in that, is benchmark with the described rubber components of 100 weight parts, and it further comprises the plant extract oil of 1～50 weight part.
3. pneumatic tyre that contains rubber composition for tire tread as claimed in claim 1.
Applications Claiming Priority (9)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2004078018 | 2004-03-18 | ||
| JP2004-078018 | 2004-03-18 | ||
| JP2004078018A JP4475992B2 (en) | 2004-03-18 | 2004-03-18 | Rubber composition for tire tread and pneumatic tire using the same |
| JP2004-084399 | 2004-03-23 | ||
| JP2004084399 | 2004-03-23 | ||
| JP2004084399A JP4338564B2 (en) | 2004-03-23 | 2004-03-23 | Rubber composition for tire tread and pneumatic tire using the same |
| JP2004-188467 | 2004-06-25 | ||
| JP2004188467A JP4583085B2 (en) | 2004-06-25 | 2004-06-25 | Rubber composition for tread and pneumatic tire using the same |
| JP2004188467 | 2004-06-25 |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB2005100539465A Division CN100378156C (en) | 2004-03-18 | 2005-03-10 | Rubber composition for tire tread and pneumatic tire using the same |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN101230157A CN101230157A (en) | 2008-07-30 |
| CN101230157B true CN101230157B (en) | 2011-09-28 |
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| CN2008100037208A Expired - Fee Related CN101230157B (en) | 2004-03-18 | 2005-03-10 | Rubber composition for tire tread and pneumatic tire using the same |
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| CN (1) | CN101230157B (en) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4805584B2 (en) * | 2005-01-21 | 2011-11-02 | 住友ゴム工業株式会社 | Rubber composition for tread and tire comprising the same |
| JP4970755B2 (en) * | 2005-08-17 | 2012-07-11 | 住友ゴム工業株式会社 | Rubber production method and rubber obtained thereby |
| JP2007099940A (en) * | 2005-10-05 | 2007-04-19 | Yokohama Rubber Co Ltd:The | Rubber composition |
| JP5234877B2 (en) * | 2005-12-19 | 2013-07-10 | 住友ゴム工業株式会社 | Rubber composition and tire having tread using the same |
| JP4823882B2 (en) * | 2005-12-19 | 2011-11-24 | 住友ゴム工業株式会社 | Rubber composition for inner liner and tire having inner liner using the same |
| JP4681536B2 (en) * | 2005-12-27 | 2011-05-11 | 住友ゴム工業株式会社 | Rubber composition for sidewall and method for producing the same |
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| JP2021107499A (en) * | 2019-12-27 | 2021-07-29 | Ｔｏｙｏ Ｔｉｒｅ株式会社 | Rubber composition for tire tread, and pneumatic tire using the same |
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Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5462979A (en) * | 1994-09-28 | 1995-10-31 | The Goodyear Tire & Rubber Company | Sulfur cured rubber composition containing epoxidized natural rubber and carboxylated nitrile rubber |
| US20010009932A1 (en) * | 1998-07-15 | 2001-07-26 | Pirelli Coordinamento Pneumatici S.P.A. | Vulcanizable rubber composition for treads of vehicle tires |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5396940A (en) * | 1993-09-17 | 1995-03-14 | The Goodyear Tire & Rubber Company | Sulfur cured rubber composition containing epoxidized natural rubber and silica filler |
| JP3363539B2 (en) * | 1993-09-20 | 2003-01-08 | 横浜ゴム株式会社 | Rubber composition for tire tread |
| US6014998A (en) * | 1998-06-09 | 2000-01-18 | Pirelli Pneumatici S.P.A. | Silica-reinforced tire compositions containing triazoles |
| JP2002533234A (en) * | 1998-12-22 | 2002-10-08 | ピレリ・プネウマティチ・ソチエタ・ペル・アツィオーニ | Tire manufacturing method, tire obtained thereby, and elastomer composition used therein |
| JP2002275311A (en) * | 2001-01-10 | 2002-09-25 | Bridgestone Corp | Rubber composition and tire |
| JP3683519B2 (en) * | 2001-08-24 | 2005-08-17 | 住友ゴム工業株式会社 | Rubber composition |
| JP4089239B2 (en) * | 2002-02-15 | 2008-05-28 | Ｊｓｒ株式会社 | Rubber composition and pneumatic tire using the same |
| JP4361322B2 (en) * | 2003-07-25 | 2009-11-11 | 住友ゴム工業株式会社 | Rubber composition for tire tread and pneumatic tire using the same |
| JP4076910B2 (en) * | 2003-06-03 | 2008-04-16 | 住友ゴム工業株式会社 | Rubber composition for tread and pneumatic tire using the same |
-
2004
- 2004-03-18 JP JP2004078018A patent/JP4475992B2/en not_active Expired - Fee Related
-
2005
- 2005-03-10 CN CN2008100037208A patent/CN101230157B/en not_active Expired - Fee Related
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5462979A (en) * | 1994-09-28 | 1995-10-31 | The Goodyear Tire & Rubber Company | Sulfur cured rubber composition containing epoxidized natural rubber and carboxylated nitrile rubber |
| US20010009932A1 (en) * | 1998-07-15 | 2001-07-26 | Pirelli Coordinamento Pneumatici S.P.A. | Vulcanizable rubber composition for treads of vehicle tires |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2005263956A (en) | 2005-09-29 |
| CN101230157A (en) | 2008-07-30 |
| JP4475992B2 (en) | 2010-06-09 |
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