KR100869904B1 - Tire tread rubber composition improved abrasion property - Google Patents

Tire tread rubber composition improved abrasion property Download PDF

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KR100869904B1
KR100869904B1 KR1020070096447A KR20070096447A KR100869904B1 KR 100869904 B1 KR100869904 B1 KR 100869904B1 KR 1020070096447 A KR1020070096447 A KR 1020070096447A KR 20070096447 A KR20070096447 A KR 20070096447A KR 100869904 B1 KR100869904 B1 KR 100869904B1
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molecular weight
silane
weight polyethylene
rubber composition
rubber
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정혜민
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금호타이어 주식회사
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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B60VEHICLES IN GENERAL
    • B60CVEHICLE TYRES; TYRE INFLATION; TYRE CHANGING; CONNECTING VALVES TO INFLATABLE ELASTIC BODIES IN GENERAL; DEVICES OR ARRANGEMENTS RELATED TO TYRES
    • B60C1/00Tyres characterised by the chemical composition or the physical arrangement or mixture of the composition
    • B60C1/0016Compositions of the tread
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/01Use of inorganic substances as compounding ingredients characterized by their specific function
    • C08K3/013Fillers, pigments or reinforcing additives
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/02Elements
    • C08K3/04Carbon
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/34Silicon-containing compounds
    • C08K3/36Silica
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/01Hydrocarbons
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K9/00Use of pretreated ingredients
    • C08K9/04Ingredients treated with organic substances
    • C08K9/06Ingredients treated with organic substances with silicon-containing compounds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L21/00Compositions of unspecified rubbers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions 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
    • C08L23/04Homopolymers or copolymers of ethene
    • C08L23/06Polyethene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L51/00Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
    • C08L51/06Compositions of graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers grafted on to homopolymers or copolymers of aliphatic hydrocarbons containing only one carbon-to-carbon double bond
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K2201/00Specific properties of additives
    • C08K2201/014Additives containing two or more different additives of the same subgroup in C08K
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02TCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO TRANSPORTATION
    • Y02T10/00Road transport of goods or passengers
    • Y02T10/80Technologies aiming to reduce greenhouse gasses emissions common to all road transportation technologies
    • Y02T10/86Optimisation of rolling resistance, e.g. weight reduction 

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
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  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Tires In General (AREA)

Abstract

A rubber composition for a tire tread is provided to improve abrasion resistance and rotation resistance of a tire thread compound by applying a silane-grafted ultrahigh molecular weight polyethylene. A rubber composition for a tire tread comprises 100 parts by weight of a base rubber; 50~90 parts by weight of at least one of carbon black and silica as a filler; and 1~20 parts by weight of silane-grafted ultrahigh molecular weight polyethylene. The silane-grafted ultrahigh molecular weight polyethylene is prepared by surface-treating a ultrahigh molecular weight polyethylene which is an ethylene homopolymer having the average molecular weight of 500 or more or an ethylene-alphaolefin copolymer, with at least one functional group selected from OH, alkoxy radical, aldehyde group, carbonyl radical, carboxyl, amine radical and nitro group; adding silane and peroxide to the surface-treated ultrahigh molecular weight polyethylene and reacting it.

Description

내마모 성능이 향상된 타이어 트레드용 고무 조성물{Tire Tread Rubber Composition Improved Abrasion Property} Tire Tread Rubber Composition Improved Abrasion Property}

본 발명은 타이어 트레드용 고무 조성물에 관한 것으로, 더욱 상세하게는 타이어 트레드용 고무 조성물에 실란-그라프팅된 초고분자량 폴리에틸렌을 포함하므로써, 타이어 컴파운드의 내마모 성능 및 회전저항 성능을 향상시킨 타이어 트레드용 고무 조성물에 관한 것이다.The present invention relates to a rubber composition for tire treads, and more particularly, to tire treads having improved wear resistance and rolling resistance performance of a tire compound by including silane-grafted ultra high molecular weight polyethylene in a rubber composition for tire treads. It relates to a rubber composition.

종래 기술로서, 대한민국 특허공개번호 제2003-0080025호에서는 초고분자량 폴리에틸렌을 사용하여 마모 성능을 향상시키고자 하였으며, 대한민국 특허공개번호 제2004-0024850호 및 대한민국 특허공개번호 제2005-0053425호에서는 무극성인 초고분자량 폴리에틸렌을 표면을 개질하여 적용함으로써 일반적인 초고분자량 폴리에틸렌과 비교하여 향상된 마모성능을 나타내고자 하였으나, 무극성인 폴리에틸렌은 고무, 실리카와 친화성이 없어 컴파운딩시 분산성과 결합력이 떨어져 공정성이 떨어질 뿐만 아니라, 초고분자량 폴리에틸렌이 가지는 원료의 마모 성능에 비해 타이어 적용시 마모성능이 크게 향상되는 효과를 나타내기 어려운 단점이 있다. In the prior art, Korean Patent Publication No. 2003-0080025 attempts to improve wear performance by using ultra high molecular weight polyethylene, and Korean Patent Publication No. 2004-0024850 and Korean Patent Publication No. 2005-0053425 are nonpolar. The ultra-high molecular weight polyethylene was applied by modifying the surface to show improved abrasion performance compared to general ultra-high molecular weight polyethylene. However, non-polar polyethylene has affinity with rubber and silica, so that the compoundability is poor due to its dispersibility and bonding ability. In comparison with the wear performance of the raw material of the ultra high molecular weight polyethylene, it is difficult to show an effect that the wear performance is greatly improved when the tire is applied.

본 발명은 상기와 같은 문제점을 해결하기 위하여, 실란-그라프팅된 초고분자량 폴리에틸렌을 적용함으로써, 타이어의 트레드 컴파운드의 내마모 성능 및 회전저항을 개선시킨 타이어 트레드용 고무 조성물을 제공하는 것을 목적으로 한다.The present invention is to provide a rubber composition for tire treads by improving the wear resistance and rolling resistance of the tread compound of the tire, by applying the silane-grafted ultra high molecular weight polyethylene in order to solve the above problems. .

본 발명에 다른 타이어 트레드용 고무 조성물은 원료고무 100중량부에 대하여, 충전제로서 카본블랙 및 실리카 중에서 1종 이상을 50~90중량부, 실란-그라프팅된 초고분자량 폴리에틸렌 1~20중량부를 포함하는 것을 특징으로 한다.The rubber composition for tire treads according to the present invention contains 50 to 90 parts by weight of at least one of carbon black and silica as a filler, and 1 to 20 parts by weight of silane-grafted ultra high molecular weight polyethylene, based on 100 parts by weight of the raw material rubber. It is characterized by.

본 발명에 사용되는 원료고무는, 그 종류에 특별히 한정하지 않고, 천연고무나 합성고무 또는 이들의 혼합고무를 사용하며, 바람직하게는 부타디엔 고무(BR), 스티렌부타디엔 고무, 부틸고무, 에피클로로 히드린고무, 니트릴고무, 수소화된 니트릴고무, 브롬화된 폴리이소부틸이소프렌-co-파라메틸스티렌(BIMS), 우레탄고무, 불소고무, 실리콘고무, 스티렌에틸렌부타디엔스티렌 공중합체 고무(SEBS), 에틸렌프로필렌고무, 에틸렌프로필렌디엔 고무(EPDM), 하이팔론고무, 클로로프렌고무, 에틸렌비닐아세테이트고무, 아크릴고무 중 단독 또는 2종 이상을 혼합하여 사용할 수 있다.The raw material rubber used in the present invention is not particularly limited to the kind thereof, and natural rubber, synthetic rubber or mixed rubber thereof is used. Preferably, butadiene rubber (BR), styrene butadiene rubber, butyl rubber and epichlorohydrin are used. Drined rubber, nitrile rubber, hydrogenated nitrile rubber, brominated polyisobutylisoprene-co-paramethylstyrene (BIMS), urethane rubber, fluorine rubber, silicone rubber, styrene ethylene butadiene styrene copolymer rubber (SEBS), ethylene propylene rubber , Ethylene propylene diene rubber (EPDM), hypalon rubber, chloroprene rubber, ethylene vinyl acetate rubber, acrylic rubber can be used alone or in combination of two or more thereof.

본 발명에 사용되는 충전제는, 그 종류는 특별히 한정하지 않고, 카본블랙 및 실리카 중에서 1종 이상을 사용하고, 총량으로 50~90중량부를 사용하는 것이 바람직한데, 50중량부 미만이면 보강효과가 떨어지므로 바람직하지 않고, 90중량부를 초과하면 고무와 결합하지 못한 충전제의 양이 많아져 마모성능이 떨어지므로 바람직하지 않다.  The type of filler used in the present invention is not particularly limited, and at least one of carbon black and silica is preferably used, and 50 to 90 parts by weight is preferably used as a total amount. It is not preferable because it is not preferable, and if it exceeds 90 parts by weight, the amount of filler that cannot be bonded with rubber increases, which is not preferable.

본 발명에 사용되는 실란-그라프팅된 초고분자량 폴리에틸렌은 실리카와의 결합력을 높여 공정성과 분산성을 동시에 향상시키기 위해서 사용한다.The silane-grafted ultra high molecular weight polyethylene used in the present invention is used to increase the bonding strength with silica and to improve processability and dispersibility simultaneously.

상기 실란-그라프팅된 초고분자량 폴리에틸렌은, 중량평균 분자량이 500만 이상인 에틸렌 단독 중합체 또는 에틸렌-알파올레핀 공중합체인 초고분자량 폴리에틸렌에 실리카와의 결합력을 높여 마모성능 및 공정성을 향상시키기 위해 관능기로 처리하고, 상기 관능기로 표면처리된 초고분자량 폴리에틸렌을 하기의 반응식으로 예시되는 바와 같이, 실란과 과산화물을 첨가하여 열을 가하여 반응시킴으로써 제조될 수 있다.The silane-grafted ultra high molecular weight polyethylene is treated with a functional group to increase the bonding strength with silica to the ethylene homopolymer or the ethylene-alpha olefin copolymer ultra high molecular weight polyethylene having a weight average molecular weight of 5 million or more and to improve wear performance and fairness. As illustrated in the following reaction scheme, the ultrahigh molecular weight polyethylene surface-treated with the functional group may be prepared by adding silane and a peroxide to react with heat.

Figure 112007068734368-pat00001
Figure 112007068734368-pat00001

상기 초고분자량 폴리에틸렌의 표면처리에 사용되는 관능기로는 실리카와 친화성이 있는 히드록시기, 알콕시기, 알데히드기, 카르보닐기, 카르복실기, 아민기, 니트로기 중에서 선택되는 하나 또는 그 이상을 사용할 수 있으며, 관능기로 표면처리된 초고분자량 폴리에틸렌의 반복단위는 하기의 구조식으로 나타낼 수 있다.As the functional group used for the surface treatment of the ultra high molecular weight polyethylene, one or more selected from hydroxy group, alkoxy group, aldehyde group, carbonyl group, carboxyl group, amine group and nitro group which have affinity with silica may be used. The repeating unit of the treated ultra high molecular weight polyethylene can be represented by the following structural formula.

Figure 112007068734368-pat00002
Figure 112007068734368-pat00002

상기 실란-그라프팅된 초고분자량 폴리에틸렌의 제조에 사용되는 실란은 폴리에틸렌과 상호결합이 좋은 비닐계 실란으로, 그 종류에 특별히 한정은 없고, 비닐트리에톡시실란(VTEOS;vinyltriethoxy silane), 비닐트리메톡시에톡시실란(VTMOEOS;vinyltrimethoxyethoxy silane), 비닐벤질아미노에틸아미노프로필트리메톡시실란([2(vinylbenzylamino)-ethyl]-3-aminopropyltrimethoxy silane), 디메틸비닐메톡시실란(DMVMOS;dimethylvinylmethoxy silane), 디메틸비닐에톡시실란(DMVEOS;dimethylvinylethoxy silane), 메틸비닐디메톡시실란(methyvinyldimethoxy silane), 메틸비닐디에톡시실란(methyvinyldimethoxy silane)중에서 선택되는 1종 이상을 사용할 수 있다. 또한, 상기의 과산화물은 디쿠밀퍼옥사이드(dicumyl peroxide)가 바람직하지만, 그 종류에 특별히 한정하지 않고, 디벤조일퍼옥사이드, 비스-퍼옥사이드-2,5-디메틸-2,5-디(t-부틸퍼옥사이드)-헥산, t-디부틸쿠밀퍼옥사이드, 디-t-부틸퍼옥사이드, 디(t-부틸퍼옥사이드)디이소프로필벤젠 중에서 선택되는 1종 이상을 사용할 수 있다.The silane used in the production of the silane-grafted ultra high molecular weight polyethylene is a vinyl-based silane having good interconnection with polyethylene, and is not particularly limited in its type, and is vinyl triethoxy silane (VTEOS) and vinyl trimeth. Vinyltrimethoxyethoxy silane (VTMOEOS), vinylbenzylaminoethylaminopropyltrimethoxysilane ([2 (vinylbenzylamino) -ethyl] -3-aminopropyltrimethoxy silane), dimethylvinmethoxymethoxysilane (DMVMOS; dimethylvinylmethoxy silane), dimethyl At least one selected from vinyl ethoxysilane (DMVEOS), methylvinyldimethoxy silane (methyvinyldimethoxy silane) and methylvinyldimethoxy silane (methyvinyldimethoxy silane) may be used. The peroxide is preferably dicumyl peroxide. However, the peroxide is not particularly limited to dibenzoyl peroxide and bis-peroxide-2,5-dimethyl-2,5-di (t-butyl). Peroxide) -hexane, t-dibutyl cumyl peroxide, di-t-butyl peroxide, di (t-butyl peroxide) diisopropyl benzene can be used 1 or more types.

상기 실란-그라프팅된 초고분자량 폴리에틸렌은 1~20중량부를 사용하는 것이 바람직한데, 1중량부 미만이면 마모성능을 나타내지 못하므로 바람직하지 않고, 20중량부를 초과하면 경도가 급격히 증가하여 크랙이 발생하므로 바람직하지 않다.The silane-grafted ultra high molecular weight polyethylene is preferably used 1 to 20 parts by weight, but less than 1 part by weight does not exhibit abrasion performance is not preferable, if exceeding 20 parts by weight because the hardness is sharply increased to cause cracks Not desirable

본 발명의 고무 조성물에는 상기한 성분들 이외에, 통상적으로 타이어 트레 드용 고무 조성물에 사용되는 첨가제들, 예로서, 실란커플링제, 아로마틱오일, 노화방지제, 산화아연, 스테아린산, 황, 촉진제, 활성제 등의 첨가제를 통상의 사용량 범위로 배합할 수 있다. In addition to the above-mentioned components, the rubber composition of the present invention includes additives that are commonly used in rubber treads, such as silane coupling agents, aromatic oils, antioxidants, zinc oxide, stearic acid, sulfur, accelerators, activators, and the like. An additive can be mix | blended in the normal usage range.

본 발명의 타이어 트레드용 고무 조성물은 실란-그라프팅된 초고분자량 폴리에틸렌을 포함하므로써, 내마모 성능 및 회전저항을 개선시키는 효과를 갖는다.The rubber composition for tire treads of the present invention includes an silane-grafted ultra high molecular weight polyethylene, and thus has an effect of improving abrasion resistance and rolling resistance.

이하 본 발명을 실시예를 통하여 더욱 상세히 설명한다. 그러나 이들 실시예가 본 발명의 범위를 제한하는 것은 아니다.Hereinafter, the present invention will be described in more detail with reference to Examples. However, these examples do not limit the scope of the present invention.

하기 표 1의 조성대로 실시예 및 비교예의 타이어 트레드 고무 조성물을 제조한 후, 각 고무 조성물로 고무 시편을 제조하여, 160℃에서 가류시킨 후 그 물성을 ASTM 규격에 따라 측정하고, 그 결과를 하기 표 2에 나타내었다. After the tire tread rubber compositions of Examples and Comparative Examples were prepared according to the composition of Table 1, rubber specimens were prepared from the respective rubber compositions, vulcanized at 160 ° C., and then the physical properties thereof were measured according to ASTM standards. Table 2 shows.

표 1Table 1

(단위:중량부)                                                     (Unit: weight part)

구분division 비교예1Comparative Example 1 실시예1Example 1 실시예2Example 2 실시예3Example 3 스티렌부타디엔고무Styrene Butadiene Rubber 100100 100100 100100 100100 실리카Silica 7070 7070 7070 7070 UHMW-PE1 ) UHMW-PE 1 ) 55 00 00 00 실란 그라프팅된 UHMW-PE2 ) Silane grafted UHMW-PE 2 ) 00 55 1010 2020 실란커플링제3 ) Silane coupling agent 3 ) 5.65.6 5.65.6 5.65.6 5.65.6 아로마틱오일Aromatic Oil 37.537.5 37.537.5 37.537.5 37.537.5 노화방지제4 ) Antioxidant 4 ) 22 22 22 22 산화아연Zinc oxide 33 33 33 33 스테아린산Stearic acid 22 22 22 22 sulfur 22 22 22 22 촉진제5 ) Accelerators 5 ) 22 22 22 22 활성제6 ) Activator 6 ) 0.50.5 0.50.5 0.50.5 0.50.5

주) 1) 초고분자량 폴리에틸렌: 중량평균 분자량이 500만 이상Note 1) Ultra high molecular weight polyethylene: weight average molecular weight is more than 5 million

2) 상기 1)의 초고분자량 폴리에틸렌을 비닐트리메톡시실란으로 그라프트화 한 것.2) The ultra-high molecular weight polyethylene of 1) is grafted with vinyltrimethoxysilane.

3) TESPT(비스-(3-트리에톡시실릴프로필)테트라설판)3) TESPT (bis- (3-triethoxysilylpropyl) tetrasulfane)

4) TMDQ(고분자화된 2,2,4-트리메틸-1,2-디히드로퀴놀린)4) TMDQ (polymerized 2,2,4-trimethyl-1,2-dihydroquinoline)

5) CZ(N-시클로헥실-2-벤조티아졸설펜아미드)5) CZ (N-cyclohexyl-2-benzothiazolesulfenamide)

6) DPG(디페닐 구아니딘) 6) DPG (diphenyl guanidine)

표 2TABLE 2

(단위: 상대지수)                                                         (Unit: relative index)

구분 division 비교예1Comparative Example 1 실시예1Example 1 실시예2Example 2 실시예3Example 3 물성  Properties 경도Hardness 100100 104104 108108 115115 300% 모듈러스300% modulus 100100 110110 117117 127127 인장강도The tensile strength 100100 9494 9595 9898 신장율Elongation 100100 9797 9595 9292 내마모성능Wear resistance DIN 마모1 ) DIN wear 1 ) 100100 115115 120120 135135 회전저항성능Rolling resistance performance 70℃ tanδ2) 70 ℃ tanδ 2) 100100 9191 8686 8080

주) 1) 마모지수는 높은수록 유리한 수치임.Note 1) The higher the wear index, the more favorable the value.

2) 회전저항성능은 낮을수록 유리한 수치를 나타냄.2) The lower the rolling resistance, the more favorable the value.

상기 표 2에서 보는 바와 같이, 실시예의 고무 조성물은 내마모 성능 및 회전저항성능이 우수함을 알 수 있다.As shown in Table 2, it can be seen that the rubber composition of the embodiment is excellent in wear resistance and rotation resistance performance.

Claims (3)

원료고무 100중량부에 대하여, 충전제로서 카본블랙 및 실리카 중에서 1종 이상을 50~90중량부 및 실란-그라프팅된 초고분자량 폴리에틸렌 1~20중량부를 포함하는 것을 특징으로 하는 타이어 트레드용 고무 조성물.A rubber composition for tire treads, comprising 50 to 90 parts by weight of at least one of carbon black and silica and 1 to 20 parts by weight of silane-grafted ultra high molecular weight polyethylene, based on 100 parts by weight of the raw material rubber. 제1항에 있어서, 실란-그라프팅된 초고분자량 폴리에틸렌은 중량평균 분자량이 500만 이상인 에틸렌 단독 중합체 또는 에틸렌-알파올레핀 공중합체인 초고분자량 폴리에틸렌에 관능기로서 히드록시기, 알콕시기, 알데히드기, 카르보닐기, 카르복실기, 아민기 및 니트로기 중에서 선택되는 하나 이상의 관능기로 표면처리된 초고분자량 폴리에틸렌에 실란과 과산화물을 첨가하여 반응시킴으로써 제조되는 것을 특징으로 하는 타이어 트레드용 고무 조성물.The silane-grafted ultra high molecular weight polyethylene according to claim 1 is a hydroxy group, an alkoxy group, an aldehyde group, a carbonyl group, a carboxyl group, an amine as a functional group in an ultra high molecular weight polyethylene which is an ethylene homopolymer or an ethylene-alpha olefin copolymer having a weight average molecular weight of 5 million or more. A rubber composition for tire treads, which is prepared by adding silane and a peroxide to a super high molecular weight polyethylene surface-treated with at least one functional group selected from a group and a nitro group. 제2항에 있어서, 상기 실란-그라프팅된 초고분자량 폴리에틸렌에 있어서의 상기 실란은 비닐계 실란인 것을 특징으로 하는 타이어 트레드용 고무 조성물.3. The rubber composition for tire tread according to claim 2, wherein the silane in the silane-grafted ultra high molecular weight polyethylene is vinyl silane.
KR1020070096447A 2007-09-21 2007-09-21 Tire tread rubber composition improved abrasion property KR100869904B1 (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2024025591A1 (en) * 2022-07-25 2024-02-01 Cooper-Standard Automotive, Inc. Fortrex additive for low rolling resistance tires

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4289860A (en) * 1974-03-08 1981-09-15 Kabel- Und Metallwerke Gutehoffnungshutte Ag Grafting of silane on thermoplastics or elastomers for purposes of cross linking
KR970027184A (en) * 1995-11-14 1997-06-24 남일 Tire Rubber Composition Containing High Molecular Agent
KR20050025962A (en) * 2002-07-09 2005-03-14 제너럴 일렉트릭 캄파니 Silica-rubber mixtures having improved hardness
JP2006188701A (en) 2004-12-30 2006-07-20 Goodyear Tire & Rubber Co:The Tread cap composition

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4289860A (en) * 1974-03-08 1981-09-15 Kabel- Und Metallwerke Gutehoffnungshutte Ag Grafting of silane on thermoplastics or elastomers for purposes of cross linking
KR970027184A (en) * 1995-11-14 1997-06-24 남일 Tire Rubber Composition Containing High Molecular Agent
KR20050025962A (en) * 2002-07-09 2005-03-14 제너럴 일렉트릭 캄파니 Silica-rubber mixtures having improved hardness
JP2006188701A (en) 2004-12-30 2006-07-20 Goodyear Tire & Rubber Co:The Tread cap composition

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2024025591A1 (en) * 2022-07-25 2024-02-01 Cooper-Standard Automotive, Inc. Fortrex additive for low rolling resistance tires

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