KR100715718B1 - Pcr tread compound for pneumatic tire - Google Patents

Pcr tread compound for pneumatic tire Download PDF

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KR100715718B1
KR100715718B1 KR1020050053937A KR20050053937A KR100715718B1 KR 100715718 B1 KR100715718 B1 KR 100715718B1 KR 1020050053937 A KR1020050053937 A KR 1020050053937A KR 20050053937 A KR20050053937 A KR 20050053937A KR 100715718 B1 KR100715718 B1 KR 100715718B1
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phr
rubber
butadiene rubber
glass transition
transition temperature
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KR20060134336A (en
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이진행
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금호타이어 주식회사
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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L9/00Compositions of homopolymers or copolymers of conjugated diene hydrocarbons
    • C08L9/06Copolymers with styrene
    • 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
    • C08K3/02Elements
    • 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
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L9/00Compositions of homopolymers or copolymers of conjugated diene hydrocarbons
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2201/00Properties
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/02Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group

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  • 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)

Abstract

본 발명은 유리전이 온도가 -35~-30℃인 용액중합 스티렌부타디엔 고무 50~70phr, 유리전이 온도가 -26~-22℃인 용액중합 스티렌부타디엔 고무 10~30phr, 부타디엔 고무 20~40phr로 이루어진 원료고무 100phr에 대하여, 카본블랙 35~55phr, 실리카 30~50phr을 포함하는 타이어 트레드용 고무 조성물에 관한 것이다.The present invention is composed of a solution-polymerized styrene butadiene rubber 50 ~ 70 phr, the glass transition temperature is -35 ~ -30 ℃, a solution polymerization styrene butadiene rubber 10 ~ 30 phr, the glass transition temperature is -26 ~-22 ℃, butadiene rubber 20 ~ 40 phr It relates to a rubber composition for tire treads containing 35 to 55 phr of carbon black and 30 to 50 phr of silica with respect to 100 phr of raw rubber.

본 발명에 따른 타이어 트레드 고무 조성물은 제동력과 연비 성능이 향상되면서도 내마모 성능이 저하하지 않는다. The tire tread rubber composition according to the present invention does not deteriorate abrasion resistance while improving braking force and fuel economy performance.

타이어 트레드 고무 조성물, 제동력, 연비 성능, 내마모 성능, 실리카 Tire tread rubber composition, braking force, fuel economy performance, wear resistance performance, silica

Description

승용차용 공기입 타이어 트레드 고무 조성물{PCR TREAD COMPOUND FOR PNEUMATIC TIRE}Pneumatic tire tread rubber composition for passenger car {PCR TREAD COMPOUND FOR PNEUMATIC TIRE}

본 발명은 내마모 성능을 떨어뜨리지 않으면서도 연비특성 및 제동력이 우수한 타이어 트레드용 고무 조성물에 관한 것이다.The present invention relates to a rubber tread rubber composition excellent in fuel efficiency and braking power without compromising wear resistance.

타이어 트레드 고무가 가져야 할 성질들은 매우 다양하여, 조종안정성, 소음, 직진성, 회전저항, 제동력, 내마모성, 내구력 등의 모든 특성을 적절히 갖추어 어떤 조건에서도 운전자의 조정력에 긴밀하게 대응하도록 하는 것이 요구된다. The properties of tire tread rubber are so diverse that it is necessary to have all the characteristics such as steering stability, noise, straightness, rolling resistance, braking force, abrasion resistance, and durability, so as to closely correspond to the driver's adjustment force under any conditions.

그러나 상기의 특성들 중에서는, 특정 성질을 향상시키기 위한 조작을 하면, 그 영향을 역으로 수용하여 다른 성질이 열화할 우려가 큰 것이 있기 때문에 타이어에 있어서 특정 성질을 개선시킨다는 것은 다른 성질들이 무익한 영향을 받지 않으면서 목적하는 성질만이 개선되어야 하는 것을 의미하므로, 그 개발에는 기술적으로 어려움이 있었다.However, among the above characteristics, there is a high possibility that other operations may be deteriorated due to the adverse effect of the operation to improve specific properties. There was a technical difficulty in its development because it meant that only the desired properties had to be improved without receiving them.

최근 환경문제가 자동차 산업 분야에서 가장 고려하여야 할 요소로 자리잡고 있기 때문에, 가능한 한 회전저항을 감소시키므로써, 연비를 줄이고자 하는 노력이 경주되어 왔다. 회전저항을 감소시켜 연비를 줄이기 위하여 카본블랙을 실리카로 바꾸어 사용하는 경우, 연비 성능은 좋아지지만 내마모 성능에 악영향을 끼쳐서 내마모성이 떨어지는 문제점이 있었다. 또한 연비성능을 올리기 위하여 실리카를 사용함으로써 고분자와의 친화성을 높이기 위하여 부수적으로 다른 첨가제를 첨가할 필요가 있거나 또는 특수한 물성을 가지는 고분자를 선택하는 경우에 원가상승이 야기되는 등의 문제점도 여전히 존재하기 때문에, 카본블랙을 일부 실리카로 대체한 경우 고무성분의 조성을 조정하므로써 별도의 첨가제 추가 등의 조작없이 연비특성이 우수하면서도 내마모 성능이 열화되지 않는 타이어 트레드용 고무 조성물에 대한 요구가 있어왔다.Recently, since environmental issues have become the most important factor in the automotive industry, efforts have been made to reduce fuel consumption by reducing rolling resistance as much as possible. When carbon black is used in place of silica in order to reduce rolling resistance and reduce fuel efficiency, fuel efficiency is improved, but there is a problem in that the wear resistance is inferior because it adversely affects the wear performance. In addition, there are still problems such as the need to add other additives in order to increase the affinity with the polymer by using silica to increase fuel efficiency, or cost increase when selecting a polymer having special physical properties. Therefore, when carbon black is replaced with some silica, there has been a demand for a rubber tread rubber composition having excellent fuel efficiency without deteriorating abrasion performance without adjusting an additive such as adding a rubber component.

본 발명의 타이어용 트레드 고무 조성물은 이러한 문제점을 해결하기 위한 것으로서, 고무성분의 조성을 조정하므로써 내마모 성능을 떨어뜨리지 않으면서 연비특성이 우수한 타이어 트레드용 고무 조성물을 제공하고자 하는 것이다.The tread rubber composition for a tire of the present invention is to solve such a problem, and to provide a rubber tread rubber composition having excellent fuel efficiency without degrading abrasion resistance by adjusting the composition of the rubber component.

본 발명은, 유리전이 온도가 -35~-30℃인 용액중합 스티렌부타디엔 고무 50~70phr, 유리전이 온도가 -26~-22℃인 용액중합 스티렌부타디엔 고무 10~30phr, 부타디엔 고무 20~40phr로 이루어진 원료고무 100phr에 대하여, 카본블랙 35~55phr, 실리카 30~50phr을 포함하는 타이어 트레드용 고무 조성물을 제공한다. The present invention is 50 to 70 phr of solution-polymerized styrene-butadiene rubber having a glass transition temperature of -35 to -30 ° C, 10 to 30 phr of solution-polymerized styrene butadiene rubber having a glass transition temperature of -26 to -22 ° C, and 20 to 40 phr of butadiene rubber. With respect to 100 phr of the raw rubber, the rubber composition for tire treads including 35 to 55 phr of carbon black and 30 to 50 phr of silica is provided.

본 발명에서는 원료고무의 성분으로서 유리전이온도(Tg)가 각각 -35~-30℃와 -26~-22℃인 2종의 용액중합 스티렌부타디엔 고무를 사용한다. In the present invention, two kinds of solution-polymerized styrene-butadiene rubbers having a glass transition temperature (Tg) of -35 to -30 ° C and -26 to -22 ° C, respectively, are used as components of the raw material rubber.

상기 유리전이온도가 -35~-30℃인 용액중합 스티렌부타디엔 고무의 사용량은 50~70phr로서, 이 함량이 50phr 미만이면 내마모성 및 내스노우성이 떨어지고, 70phr을 초과하면 핸들링 성능이 부족하여 바람직하지 않다. The amount of the solution-polymerized styrene-butadiene rubber having a glass transition temperature of -35 to 30 ° C. is 50 to 70 phr, and if the content is less than 50 phr, wear resistance and snow resistance are lowered. not.

또한 유리전이온도가 -26~-22℃인 용액중합 스티렌부타디엔 고무의 사용량은 10~30phr로서, 이 함량이 10phr 미만이면 핸들링 성능이 떨어지고, 30phr을 초과하면 연비 및 내마모성이 하락하여 바람직하지 않다. In addition, the amount of the solution-polymerized styrene-butadiene rubber having a glass transition temperature of -26 ~ -22 ℃ is 10 ~ 30phr, when the content is less than 10phr, the handling performance is lowered, if it exceeds 30phr it is not preferable because the fuel efficiency and wear resistance decreases.

상기 유리전이온도가 -35~-30℃인 용액중합 스티렌부타디엔 고무와 유리전이온도가 -26~-22℃인 용액중합 스티렌부타디엔 고무는 유리전이온도가 각각 상기 범위라면 그 종류에 특별히 제한이 없으며, 시판되는 제품으로는 각각 SOLFLEX-2535X(상품명, 스티렌 함량 25중량%, 비닐 함량 35중량%, Tg -32℃, 미국 굿이어(사)제품)와 SE SLR-4601(상품명, 스티렌 함량 21중량%, 비닐 함량 63중량%, Tg -24.5℃, 미국 다우(사)제품)를 들 수 있다. The solution-polymerized styrene-butadiene rubber having a glass transition temperature of -35 to -30 ° C and the solution-polymerized styrene-butadiene rubber having a glass transition temperature of -26 to -22 ° C are not particularly limited as long as the glass transition temperature is in the above range. Commercially available products include SOLFLEX-2535X (brand name, styrene content 25% by weight, vinyl content 35% by weight, Tg -32 ℃, Goodyear USA) and SE SLR-4601 (brand name, styrene content 21%). %, Vinyl content 63 weight%, Tg-24.5 degreeC, the Dow Corporation of America) is mentioned.

본 발명에서는, 상기 2종의 용액중합 스티렌부타디엔 고무외에 원료고무 성분으로서 부타디엔 고무를 사용한다. 본 발명에서 사용되는 부타디엔 고무로는, 특히 시스함량이 높은 부타디엔 고무를 사용하는 것이 바람직하다. 부타디엔 고무의 시스함량은 98중량% 이상인 것이 바람직하다. 부타디엔 고무의 시스함량이 98중량% 미만이면, 내마모성이 저하할 우려가 있다. 본 발명에 사용할 수 있는 부타디엔 고무로서는, 시스함량이 높은 것이라면 그 종류에 특별한 제한은 없으며, 시판되는 제품으로는 Nd-BR(상품명, 시스함량 98중량%, 니트릴 함량 10중량%, Tg -105℃, 바이엘사제품)을 들 수 있다. In the present invention, butadiene rubber is used as the raw material rubber component in addition to the two kinds of solution-polymerized styrene butadiene rubbers. As butadiene rubber used for this invention, it is preferable to use butadiene rubber with high cis content especially. It is preferable that the cis content of butadiene rubber is 98 weight% or more. If the sheath content of butadiene rubber is less than 98% by weight, there is a fear that the wear resistance is lowered. The butadiene rubber which can be used in the present invention is not particularly limited as long as it has a high cis content, and commercially available products include Nd-BR (trade name, cis content 98 wt%, nitrile content 10 wt%, and Tg -105 ° C). Bayer company) is mentioned.

본 발명의 고무 조성물에서 부타디엔 고무를 20phr 미만으로 함유하는 경우 에는 내마모 성능이 불충분하고, 40phr을 초과하여 함유하는 경우에는 내마모 성능은 크게 개선되지만 제동력 등이 열화한다.In the rubber composition of the present invention, when the butadiene rubber is contained in less than 20 phr, the wear resistance is insufficient. When the rubber composition contains more than 40 phr, the wear resistance is greatly improved, but the braking force and the like deteriorate.

본 발명에서 보강재로 사용되는 카본블랙은 그 등급에 특별한 제한이 없으며, 사용량은 35~55phr의 범위가 바람직하다. 카본블랙의 함량이 35phr 미만이면 내마모성 및 강성 등의 기계적 물성이 저하할 우려가 있고, 55phr을 초과하면, 회전저항이 높아져서 연비가 상승할 우려가 있으므로 바람직하지 않다.Carbon black used as a reinforcing material in the present invention is not particularly limited in its grade, the amount is preferably in the range of 35 ~ 55phr. If the content of carbon black is less than 35 phr, mechanical properties such as wear resistance and rigidity may be lowered. If the content of carbon black is more than 55 phr, rotational resistance may be increased and fuel efficiency may be increased, which is not preferable.

본 발명에서 카본블랙과 함께 사용되는 실리카는 그 종류에 특별한 제한이 없으며, 사용량은 30~50phr의 범위가 바람직하다. 실리카의 함량이 30phr 미만이면 연비성능 향상효과가 미흡하고, 50phr을 초과하면 내마모성능이 저하하므로 바람직하지 않다.   Silica used in combination with the carbon black in the present invention is not particularly limited in its kind, the amount is preferably in the range of 30 ~ 50phr. If the content of silica is less than 30 phr, the fuel efficiency improvement effect is insufficient. If the content of silica is more than 50 phr, the wear resistance is lowered.

본 발명의 고무 조성물에는 상기한 성분들 이외에, 통상적으로 타이어 트레드용 고무 조성물에 사용되는 첨가제들, 예로서 연화제, 활성제, 노방제, 가류제, 촉진제 등의 첨가제를 통상의 사용량 범위로 사용할 수 있다. In addition to the above-mentioned components, the rubber composition of the present invention may be used additives, which are commonly used in rubber tread rubber compositions, for example, additives such as softeners, activators, lubricating agents, vulcanizing agents, accelerators, etc. in the usual usage ranges. .

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.

실시예 및 비교예Examples and Comparative Examples

표 1의 조성에 따라 고무 조성물을 제조하고, 그 물성치를 시험하여 표 1에 나타내었다.A rubber composition was prepared according to the composition of Table 1, and the physical properties thereof were tested and shown in Table 1.

ASTM D113184-80에 따라 용량 1.6L 밀폐식 혼합기(BR LAB BANBURY MIXER, FARREL CO.) 내에서 가류제와 촉진제를 제외한 각각의 원료를 40rpm으로 배합하여 카본블랙마스터 배치를 제조한 후, 가류제와 촉진제를 넣고 30rpm으로 60초간 최종배합하였다. 이 배합된 고무를 160℃에서 20분간 가류한 후, 시편을 제조하였다. 인장물성은 ASTM D-412에 따라 인장시험기(INSTRON 6012)를 이용하여 상온에서 측정하였다.According to ASTM D113184-80, a carbon black master batch was prepared by blending each raw material except the vulcanizing agent and the accelerator at 40 rpm in a capacity 1.6 L sealed mixer (BR LAB BANBURY MIXER, FARREL CO.), A vulcanizing agent and a promoter were added and final blended at 30 rpm for 60 seconds. This blended rubber was vulcanized at 160 ° C. for 20 minutes to prepare a specimen. Tensile properties were measured at room temperature using a tensile tester (INSTRON 6012) according to ASTM D-412.

표 1 고무 조성물의 배합비 및 그에 따른 물성치 (단위:phr) Table 1 Mixing ratio of rubber composition and its physical properties (unit: phr)

구분division 실시예1Example 1 실시예2Example 2 실시예3Example 3 비교예1Comparative Example 1 비교예2Comparative Example 2 비교예3Comparative Example 3 고무 Rubber SOLFLEX-2535X1) SOLFLEX-2535X 1) 50(오일포함68.5)50 (68.5 including oil) SE-SLR-46012) SE-SLR-4601 2) 3030 2020 1010 5050 4040 00 Nd-BR3) Nd-BR 3) 2020 3030 4040 00 1010 5050 연화제Softener 오일4) Oil 4) 5.005.00 5.005.00 5.005.00 7.007.00 3.003.00 5.005.00 활성제Active agent ZnO#SZnO # S 3.003.00 3.003.00 3.003.00 3.003.00 3.003.00 3.003.00 카본블랙Carbon black N-375N-375 4040 4040 4040 7575 4040 4040 실리카Silica z-175z-175 4040 4040 4040 -- 4040 4040 노방제 Labor K-RD5) K-RD 5) 2.002.00 2.002.00 2.002.00 2.002.00 2.002.00 2.002.00 K-136) K-13 6) 2.002.00 2.002.00 2.002.00 2.002.00 2.002.00 2.002.00 Sunnoc7) Sunnoc 7) 2.002.00 2.002.00 2.002.00 2.002.00 2.002.00 2.002.00 활성제Active agent S/AS / A 2.002.00 2.002.00 2.002.00 2.002.00 2.002.00 2.002.00 가류제Vulcanizing agent sulfur 2.002.00 2.002.00 2.002.00 2.002.00 2.002.00 2.002.00 촉진제 accelerant CZ8) CZ 8) 1.801.80 1.801.80 1.801.80 1.801.80 1.801.80 1.801.80 DPG(가류촉진제)9) DPG (vulcanization accelerator) 9) 0.450.45 0.450.45 0.450.45 0.450.45 0.450.45 0.450.45 인강물성 (초기)  Toughness (Initial) 경도Hardness 7171 6969 6969 6565 7272 6565 300% 모듈러스 (㎏/㎠)300% modulus (㎏ / ㎠) 137137 133133 113113 103103 138138 110110 인장강도(㎏/㎠)Tensile Strength (㎏ / ㎠) 201201 217217 208208 202202 218218 215215 신율(%)% Elongation 458458 437437 445445 490490 451451 510510 동적 인장물성 Dynamic tensile properties Tg(0℃)Tg (0 ° C) -21-21 -26-26 -30-30 -11-11 -16-16 -35-35 Tanδ(0℃)10) Tanδ (0 ° C) 10) 0.3190.319 0.3020.302 0.2500.250 0.2120.212 0.3390.339 0.2230.223 Tanδ(70℃)11) Tanδ (70 ° C) 11) 0.1010.101 0.0900.090 0.0890.089 0.1650.165 0.0950.095 0.0900.090 리바운드rebound 1st1st 17.417.4 20.120.1 20.420.4 12.1212.12 16.416.4 21.321.3 내마모성Wear resistance PICO(g)12) PICO (g) 12) 0.0350.035 0.0290.029 0.0290.029 0.0300.030 0.0380.038 0.0280.028

주1)SOLFLEX-2535X : 용액중합-SBR; 스티렌 25중량%, 비닐 35중량%, 유리전이온도 -32℃, 미국 굿이어(사) 제조 Note 1) SOLFLEX-2535X: solution polymerization-SBR; Styrene 25% by weight, vinyl 35% by weight, glass transition temperature -32 ℃, manufactured by Goodyear USA

주2)SE SLR-4601 : 용액중합-SBR; 스티렌 21중량%, 비닐 63중량%, 유리전이온도 -24.5℃, 미국 다우(사) 제조 Note 2) SE SLR-4601: solution polymerization-SBR; 21 wt% styrene, 63 wt% vinyl, glass transition temperature -24.5 ° C, manufactured by Dow, USA

주3)Nd-BR고무 : 시스 98중량%, 니트릴 10중량%, 유리전이온도 -105℃, 바이엘사 제조, Note 3) Nd-BR Rubber: Sheath 98% by weight, nitrile 10% by weight, glass transition temperature -105 ℃, Bayer,

주4)오일 : 방향족 오일 Note 4) Oil: aromatic oil

주5)K-RD : 2,2,4-트리메틸-1,2-디히드로퀴놀린, 금호석유화학(주) 제조 Note 5) K-RD: 2,2,4-trimethyl-1,2-dihydroquinoline, manufactured by Kumho Petrochemical Co., Ltd.

주6)K-13 : 플렉시스사 제조. Note 6) K-13 is manufactured by Flexis.

주7)Sunnoc : 하이드로카본 왁스, 용진유화 제조 Note 7) Sunnoc: Hydrocarbon Wax, Yongjin Oil

주8)CZ : N-시클로헥실-2-벤조티아졸설펜아미드, 동양제철화학(주) 제조 Note 8) CZ: N-cyclohexyl-2-benzothiazole sulfenamide, manufactured by Dongyang Steel Chemical Co., Ltd.

주9)DPG : 1,3-디페닐구아니딘, 금호석유화학(주) 제조 Note 9) DPG: 1,3-diphenylguanidine, manufactured by Kumho Petrochemical Co., Ltd.

주10)Tanδ(0℃) : 값이 높을수록 제동력이 우수하다. Note 10) Tanδ (0 ℃): The higher the value, the better the braking force.

주11)Tanδ(70℃) : 값이 낮을수록 회전저항이 낮아 연비성능이 우수하다. Note 11) Tanδ (70 ℃): The lower the value, the lower the rolling resistance.

주12)PICO(g): 어브레이션 테스트 결과, 마모된 정도를 g수로 나타낸 것으로 값이 적을수록 내마모성이 우수하다. Note 12) PICO (g): As a result of the abrasion test, the degree of wear is expressed in grams. The smaller the value, the better the wear resistance.

상기 표 1의 결과에서 알 수 있듯이 실리카와 시스함량이 높은 부타디엔 고무를 전혀 사용하지 않은 비교예1에 비하여, 본 발명의 실시예 1~3은 내마모성능은 뒤떨어지지 않으면서, 제동력 및 연비성능은 현저히 개선된 것을 확인할 수 있다. As can be seen from the results of Table 1, in comparison with Comparative Example 1 in which no butadiene rubber having high silica and cis content is used, Examples 1 to 3 of the present invention do not deteriorate abrasion resistance and brake performance and fuel efficiency. It can be seen that the remarkable improvement.

또한, 2종의 용액중합 스티렌부타디엔 고무를 모두 사용하기는 하였으나, 그 함량이 본 발명의 범위를 벗어나는 비교예 2에 비하여, 본 발명의 실시예 1~3은 내마모성능이 더 우수함을 확인할 수 있고, 용액중합 스티렌 부타디엔 고무를 1종만 고함량으로 사용한 비교예 3의 고무 조성물에 비하여, 본 발명의 실시예 1~3의 고무 조성물은 내마모 성능을 동등 수준으로 유지하면서, 제동력이 개선되었음을 확인할 수 있다. In addition, although both of the two types of solution-polymerized styrene-butadiene rubber was used, compared to Comparative Example 2, the content of which is outside the scope of the present invention, Examples 1 to 3 of the present invention can be confirmed that the wear resistance is better, Compared to the rubber composition of Comparative Example 3 using only one kind of solution-polymerized styrene butadiene rubber, it can be confirmed that the rubber composition of Examples 1 to 3 of the present invention was improved while maintaining the wear resistance at an equivalent level. .

본 발명에 따른 타이어 트레드 고무 조성물은 제동력과 연비 성능이 향상되면서도 내마모성능이 저하하지 않는다. The tire tread rubber composition according to the present invention does not deteriorate abrasion resistance while improving braking force and fuel efficiency.

Claims (2)

유리전이 온도가 -35~-30℃인 용액중합 스티렌부타디엔 고무 50~70phr, 유리전이 온도가 -26~-22℃인 용액중합 스티렌부타디엔 고무 10~30phr, 부타디엔 고무 20~40phr로 이루어진 원료고무 100phr에 대하여, 카본블랙 35~55phr, 실리카 30~50phr을 포함하는 타이어 트레드용 고무 조성물.100phr of raw material rubber consisting of solution-polymerized styrene-butadiene rubber with glass transition temperature of -35 ~ -30 ℃, 10 ~ 30phr of solution-polymerized styrenebutadiene rubber with glass transition temperature of -26 ~ -22 ℃, and 20 ~ 40phr of butadiene rubber About, the rubber composition for tire treads containing 35-55 phr of carbon black and 30-50 phr of silica. 제 1항에 있어서, 상기 부타디엔 고무는 시스함량이 98중량% 이상인 것을 특징으로 하는 타이어 트레드용 고무 조성물.The rubber composition for tire treads according to claim 1, wherein the butadiene rubber has a sheath content of 98% by weight or more.
KR1020050053937A 2005-06-22 2005-06-22 Pcr tread compound for pneumatic tire KR100715718B1 (en)

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101132780B1 (en) 2009-12-22 2012-04-09 한국타이어 주식회사 Rubber composition for tire tread and tire manufactured by using the same
KR101315118B1 (en) * 2010-11-30 2013-10-07 한국타이어 주식회사 Rubber composition for tire tread and tire manufactured by using the same

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* Cited by examiner, † Cited by third party
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KR100760823B1 (en) * 2006-10-04 2007-10-04 한국타이어 주식회사 Rubber composition for tire tread

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JPH08295759A (en) * 1995-04-21 1996-11-12 Goodyear Tire & Rubber Co:The Tire having tread of cap/base structure
JPH1160816A (en) * 1997-08-07 1999-03-05 Toyo Tire & Rubber Co Ltd Rubber composition for tire tread
KR100205484B1 (en) 1997-01-13 1999-07-01 신형인 Rubber composition of abrasion resistance for tire tread
KR20020037601A (en) * 2000-11-15 2002-05-22 조충환 Tire tread composition
KR100544526B1 (en) 2003-04-17 2006-01-23 금호타이어 주식회사 Tread compound for tire

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Publication number Priority date Publication date Assignee Title
JPH08295759A (en) * 1995-04-21 1996-11-12 Goodyear Tire & Rubber Co:The Tire having tread of cap/base structure
KR100205484B1 (en) 1997-01-13 1999-07-01 신형인 Rubber composition of abrasion resistance for tire tread
JPH1160816A (en) * 1997-08-07 1999-03-05 Toyo Tire & Rubber Co Ltd Rubber composition for tire tread
KR20020037601A (en) * 2000-11-15 2002-05-22 조충환 Tire tread composition
KR100544526B1 (en) 2003-04-17 2006-01-23 금호타이어 주식회사 Tread compound for tire

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101132780B1 (en) 2009-12-22 2012-04-09 한국타이어 주식회사 Rubber composition for tire tread and tire manufactured by using the same
KR101315118B1 (en) * 2010-11-30 2013-10-07 한국타이어 주식회사 Rubber composition for tire tread and tire manufactured by using the same

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