KR100635608B1 - Tire tread rubber composition for improving good extrusion - Google Patents

Tire tread rubber composition for improving good extrusion Download PDF

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KR100635608B1
KR100635608B1 KR1020050054188A KR20050054188A KR100635608B1 KR 100635608 B1 KR100635608 B1 KR 100635608B1 KR 1020050054188 A KR1020050054188 A KR 1020050054188A KR 20050054188 A KR20050054188 A KR 20050054188A KR 100635608 B1 KR100635608 B1 KR 100635608B1
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rubber
weight
parts
rubber composition
tire tread
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KR1020050054188A
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Korean (ko)
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조치훈
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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
    • C08K3/10Metal compounds
    • 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
    • C08L21/00Compositions of unspecified rubbers
    • 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
    • C08K3/08Metals
    • C08K2003/0893Zinc
    • 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
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20Oxides; Hydroxides
    • C08K3/22Oxides; Hydroxides of metals
    • C08K2003/2296Oxides; Hydroxides of metals of zinc
    • 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

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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)

Abstract

Provided are a tire tread rubber composition which is enhanced in extrusion, durability and heat generation characteristics, is reduced in viscosity and is improved in processability, and a tire containing the tread comprising the composition. The composition comprises 1-5 parts by weight of zinc 2-ethyl hexanoate as the dispersion aid of a reinforcing agent based on 100 parts by weight of a rubber material. Preferably the rubber material is selected from a natural rubber, a synthetic rubber or a mixture of a natural rubber and a synthetic rubber in a ratio of 1:9 to 9:1. Optionally the composition comprises further carbon black, or a mixture of carbon black and silica as a reinforcing agent.

Description

압출성이 향상된 타이어 트레드 고무조성물{Tire tread rubber composition for improving good extrusion}Tire tread rubber composition for improving good extrusion

본 발명은 압출성이 향상된 타이어 트레드 고무조성물에 관한 것으로서 보다 상세하게는 종래 타이어 트레드 고무조성물에 있어서, 아연-2-에틸-헥사노에이트(Zinc-2-ethyl-hexanoate, ZEH)를 사용하여 타이어 트레드 고무조성물의 점도를 낮추어 고무조성물의 압출공정시 발열에 의한 스코치(scorch)를 방지하고 생산성을 향상시킬 수 있는 타이어 트레드 고무조성물에 관한 것이다.The present invention relates to a tire tread rubber composition with improved extrudability. More specifically, in a conventional tire tread rubber composition, a tire using zinc-2-ethyl-hexanoate (ZEH) is used. It relates to a tire tread rubber composition that can lower the viscosity of the tread rubber composition to prevent scorch due to heat generation during the extrusion process of the rubber composition and improve productivity.

일반적으로 타이어 트레드는 천연고무와 합성고무를 주원료로 하여 주원료의 고무재료의 물성, 기타 특성을 향상시키기 위해 보강재, 노화방지제, 연화제, 가류제 및 가류촉진제를 적의 선택하고 적절한 함량으로 사용하여 우수한 내마모성을 가지도록 하고 있다. In general, tire treads are made of natural rubber and synthetic rubber as the main raw materials to improve the physical properties and other properties of the rubber materials of the main raw materials, and reinforcement, anti-aging agents, softeners, vulcanizing agents, and vulcanization accelerators are selected appropriately and used in an appropriate amount. To have.

타이어에 있어서 트레드는 차량이 이동하면서 지면과 직접 접촉하는 부위로서 타이어와 지면과의 마찰과 이러한 마찰에 의해 발생하는 열에 의해 트레드 부분이 점차적으로 마모되기 때문에 내마모 성능(abrasion resistance)이 우수해야 한 다. 또한 차량은 직진 뿐만 아니라 곡선으로 회전하기 때문에 차량의 회전에 따라 타이어의 회전저항(rolling resistance) 성능이 좋아야 한다. 그리고 비에 의해 노면이 젖거나, 동절기에 발생하는 결빙이나 빙판에 의해 노면이 젖는 경우가 많으므로 젖은 노면에서의 타이어의 미끄럼 방지 성능(wet traction)이 우수해야 한다. In the tire, the tread is an area in direct contact with the ground as the vehicle moves, and the abrasion resistance should be excellent because the tread portion is gradually worn out by friction between the tire and the ground and the heat generated by the friction. All. In addition, since the vehicle rotates in a curve as well as straight, the rolling resistance of the tire should be good as the vehicle rotates. In addition, since the road surface gets wet due to rain or the road surface is often wetted by freezing or ice generated during the winter, the wet traction of the tire on the wet road surface should be excellent.

종래 타이어 트레드 고무조성물은 보강재로 주로 카본블랙을 사용하는데 이때 다량의 카본블랙을 사용하여 고무의 인장물성과 내마모성을 증가시키고 있다. 그러나 보강재로서 다량의 카본블랙을 사용하는 경우 고무조성물의 점도가 상승되어 고무의 압출공정에서 여러 가지 문제점이 발생하고 있다. 특히 점도가 높은 고무조성물은 압출기를 통과할 때 고무와 스크류 또는 고무와 구금과의 마찰로 인해 열발생이 심화되어 스코치가 발생하고, 압출물의 형상이 변화는 문제점이 있다. Conventional tire tread rubber composition mainly uses carbon black as a reinforcing material, and a large amount of carbon black is used to increase the tensile property and wear resistance of the rubber. However, when a large amount of carbon black is used as the reinforcing material, the viscosity of the rubber composition is increased, which causes various problems in the rubber extrusion process. In particular, a rubber composition having a high viscosity has a problem in that heat generation is deepened due to friction between rubber and a screw or a mold and a scorch when passing through an extruder, and the shape of the extrudate is changed.

상기에서 언급한 문제를 해결하기 위한 안출된 본 발명은 타이어 트래드 고무조성물에 있어서, 보강재의 분산성을 향상시킬 수 있는 분산조제를 첨가하여 점도를 감소시켜 고무조성물을 압출시 점도를 낮추어 고무조성물의 압출공정시 발열에 의한 스코치를 방지하고 생산성을 향상시킬 수 있는 타이어 트레드 고무조성물의 제공을 목적으로 한다.The present invention devised to solve the problems mentioned above, in the tire tread rubber composition, by adding a dispersing aid that can improve the dispersibility of the reinforcing material to reduce the viscosity by extruding the rubber composition to reduce the viscosity of the rubber composition It is an object of the present invention to provide a tire tread rubber composition that can prevent scorch due to heat generation during the extrusion process and improve productivity.

또한 본 발명은 상기의 고무조성물로 이루어진 트레드를 함유하는 타이어의 제공을 다른 목적으로 한다.Another object of the present invention is to provide a tire containing a tread made of the above rubber composition.

상기에서 언급한 목적을 달성하기 위한 본 발명의 타이어 트레드 고무조성물은 종래 타이어 트레드 고무조성물에 있어서, 원료고무 100중량부에 대하여 분산조제로서 아연-2-에틸-헥사노에이트(Zinc-2-ethyl-hexanoate) 1∼5중량부 포함할 수 있다.The tire tread rubber composition of the present invention for achieving the above-mentioned object is zinc-2-ethyl-hexanoate (Zinc-2-ethyl) as a dispersing aid with respect to 100 parts by weight of the raw rubber in the conventional tire tread rubber composition -hexanoate) may comprise 1 to 5 parts by weight.

본 발명에서 원료고무는 종래 타이어 트레드 고무조성물의 원료고무로서 사용할 수 있는 것이라면 어떠한 것이라도 사용할 수 있다. 본 발명에서 이러한 원료고무의 일예로서 천연고무나 용액중합 스티렌 부타디엔 고무, 유화중합 스티렌 부타디엔 고무, 부타디엔 고무, 이소프렌이 함유된 스티렌 부타디엔 고무, 니트릴을 포함하는 스티렌 부타디엔 고무, 네오프렌 고무와 같은 합성고무를 각각 단독으로 사용하거나 또는 두 개의 합성고무가 1:9∼9:1의 비로 혼합된 혼합고무, 또는 세 개 이상의 합성고무가 혼합된 혼합고무를 사용할 수 있다. 또한 상기의 천연고무와 합성고무가 1:9∼9:1의 비로 혼합된 혼합고무를 사용할 수 있다.In the present invention, the raw material rubber can be used as long as it can be used as the raw material rubber of the conventional tire tread rubber composition. Examples of such raw rubbers in the present invention include synthetic rubbers such as natural rubber, solution-polymerized styrene butadiene rubber, emulsion polymerization styrene butadiene rubber, butadiene rubber, styrene butadiene rubber containing isoprene, styrene butadiene rubber containing nitrile, and neoprene rubber. Each may be used alone or a mixture of two synthetic rubbers in a ratio of 1: 9 to 9: 1, or a mixture of three or more synthetic rubbers may be used. In addition, it is possible to use a mixture of the natural rubber and synthetic rubber mixed in a ratio of 1: 9 to 9: 1.

본 발명의 타이어 트레드 고무조성물은 보강재로서 카본블랙을 단독으로 사용하거나 또는 카본블랙과 실리카를 동시에 사용할 수 있다.The tire tread rubber composition of the present invention may use carbon black alone or carbon black and silica as a reinforcing material.

본 발명에서 보강재로 카본블랙을 단독으로 사용하는 경우 카본블랙은 원료고무 100중량부에 대하여 40∼65중량부 사용할 수 있으며, 이때 카본블랙은 표면적(surface area)을 나타내는 BET값이 120∼160m2/g이고, 구조(structure)를 나타내는 DBP흡착량이 110∼160ml/100g인 것을 사용할 수 있다.When carbon black is used alone as a reinforcing material in the present invention, carbon black may be used in an amount of 40 to 65 parts by weight based on 100 parts by weight of the raw material rubber, wherein the carbon black has a BET value of 120 to 160 m 2 indicating a surface area. / g, and the DBP adsorption amount which shows a structure can be used that is 110-160 ml / 100g.

본 발명에서 보강재로 실리카를 카본블랙과 같이 적용하는 경우 실리카는 원료고무 100중량부에 대하여 5∼25중량부 사용할 수 있으며, 이때 실리카는 표면적(surface area)을 나타내는 BET값이 150∼200m2/g이고, 구조(structure)를 나타내는 DBP흡착량이 240∼300ml/100g인 것을 사용할 수 있다.When silica is used as the reinforcing material in the present invention as carbon black, silica may be used in an amount of 5 to 25 parts by weight based on 100 parts by weight of the raw material rubber, wherein silica has a BET value representing a surface area of 150 to 200 m 2 /. g, and the DBP adsorption amount which shows a structure can be used that is 240-300 ml / 100g.

본 발명에서 보강재로 카본블랙과 실리카의 혼합물을 사용하는 경우 상기에서 언급한 각각의 특성을 지닌 카본블랙은 원료고무 100중량부에 대하여 40∼65중량부 사용할 수 있으며, 실리카는 원료고무 100중량부에 대하여 5∼25중량부 사용할 수 있다.When using a mixture of carbon black and silica as a reinforcing material in the present invention, the carbon black having the above-mentioned characteristics may be used in an amount of 40 to 65 parts by weight based on 100 parts by weight of the raw material rubber, and the silica is 100 parts by weight of the raw material rubber. It can be used 5 to 25 parts by weight.

본 발명의 필수 구성 성분인 분산조제는 원료고무 100중량부에 대하여 아연-2-에틸-헥사노에이트(Zinc-2-ethyl-hexanoate, ZEH)를 1∼5중량부 사용할 수 있다. 이때 아연-2-에틸-헥사노에이트는 아연 함량이 6∼10%, 실리카 함량이 30∼35%, 보다 바람직하게는 아연 함량이 8%, 실리카 함량이 33%인 아연-2-에틸-헥사노에이트를 사용할 수 있다.Dispersion aids, which are essential components of the present invention, may be used in an amount of 1 to 5 parts by weight of zinc-2-ethyl-hexanoate (ZEH) based on 100 parts by weight of the raw material rubber. In this case, zinc-2-ethyl-hexanoate has a zinc content of 6-10%, a silica content of 30-35%, more preferably a zinc content of 8%, and a silica content of 33% zinc-2-ethyl-hexanoate. Noate can be used.

본 발명에서 분산조제인 아연-2-에틸-헥사노에이트를 원료고무 100중량부에 대하여 1중량부 미만 사용하면 타이어 트레드 고무조성물의 점도 감소가 미미하여 이 분산조제를 사용하는 의미가 없으며, 아연-2-에틸-헥사노에이트를 5중량부 초과 사용하면 고무조성물의 점도 감소에 대한 뚜렷한 효과의 상승이 생기지 않는다. 따라서 본 발명에서 아연-2-에틸-헥사노에이트는 원료고무 100중량부에 대하여 1∼5중량부 사용하는 것이 좋다.In the present invention, when zinc-2-ethyl-hexanoate, a dispersion aid, is used in an amount of less than 1 part by weight based on 100 parts by weight of the raw material rubber, the viscosity decrease of the tire tread rubber composition is insignificant. Use of more than 5 parts by weight of 2-ethyl-hexanoate does not cause a marked increase in the effect of reducing the viscosity of the rubber composition. Therefore, in the present invention, zinc-2-ethyl-hexanoate may be used in an amount of 1 to 5 parts by weight based on 100 parts by weight of the raw material rubber.

한편 본 발명에서 분산조제로 사용하는 아연-2-에틸-헥사노에이트(Zinc-2-ethyl-hexanoate, ZEH)는 시중에서 시판중인 것을 사용할 수 있다.Meanwhile, zinc-2-ethyl-hexanoate (ZEH) used as a dispersing aid in the present invention may be a commercially available one.

한편, 본 발명은 상기에서 언급한 원료고무, 보강재, 분산조제에 대하여 다양한 특성, 함량에 대하여 이들을 타이어 트레드 고무조성물에 적용한바, 본 발명의 목적을 달성하기 위해서 상기에서 언급한 특성, 함량의 원료고무, 보강재, 분산조제의 특성을 지닌 것을 사용하는 것이 좋다.On the other hand, the present invention is applied to the tire tread rubber composition for a variety of properties, contents for the above-mentioned raw rubber, reinforcing materials, dispersion aids, the raw materials of the above-mentioned properties, content to achieve the object of the present invention It is recommended to use rubber, reinforcing materials, and dispersing agents.

본 발명은 상기에서 언급한 원료고무, 보강재 이외에 종래 타이어 트레드 고무조성물에 사용되는 활성제, 연화제, 노화방지제, 공정유, 가류제 및 가류촉진제와 같은 각종 첨가제를 필요에 따라 적의 선택하여 소정의 함량으로 사용할 수 있다. 그러나 이들은 종래 타이어 트레드 고무조성물에 사용되는 일반적인 성분으로서 본원발명의 필수 구성 성분이 아니므로 이하 자세한 내용은 생략하기로 한다.According to the present invention, various additives such as activators, softeners, anti-aging agents, process oils, vulcanizing agents, and vulcanization accelerators, which are used in conventional tire tread rubber compositions, in addition to the above-mentioned raw rubbers and reinforcing materials, may be appropriately selected as necessary. Can be used. However, these are general components used in conventional tire tread rubber compositions and are not essential components of the present invention.

한편 본 발명은 상기의 타이어 트레드 고무조성물로 이루어진 트레드를 가지는 타이어를 포함한다. 이때 타이어는 오토바이용 타이어, 비행기용 타이어, 자동차용 타이어, 트럭용 타이어, 버스용 타이어 중에서 선택된 어느 하나이며, 보다 바람직하게는 트럭용 타이어, 버스용 타이어를 포함한다.On the other hand, the present invention includes a tire having a tread made of the tire tread rubber composition. In this case, the tire is any one selected from among motorcycle tires, airplane tires, automobile tires, truck tires, and bus tires, and more preferably includes truck tires and bus tires.

이하 본 발명을 다음의 비교예, 실시예, 시험예에 의하여 설명하고자 한다. 그러나 이들은 본 발명의 일실시예로서 이들에 의해 본 발명의 권리범위가 한정되는 것은 아니다. Hereinafter, the present invention will be described by the following comparative examples, examples and test examples. However, these are not limited to the scope of the present invention by these as an embodiment of the present invention.

<비교예>Comparative Example

천연고무(NR) 60중량부, 부타디엔 고무 40중량부로 이루어진 원료고무 100중량부에 대하여 카본블랙 57중량부, 실리카 5중량부, 실란커플링제(SI-69) 1.5중량부, 공정오일(Aromatic-2) 6중량부, 스테아린산(Stearic acid) 1.5중량부, 산화아연(ZnO) 3중량부, 노화방지제(RD) 6중량부를 밴버리 믹서에 넣고 150℃에서 30분 동안 배합한 후 방출하였다.57 parts by weight of carbon black, 5 parts by weight of silica, 1.5 parts by weight of silane coupling agent (SI-69), and process oil (Aromatic-) based on 100 parts by weight of raw rubber comprising 60 parts by weight of natural rubber (NR) and 40 parts by weight of butadiene rubber. 2) 6 parts by weight, stearic acid (1.5% by weight stearic acid), 3 parts by weight of zinc oxide (ZnO), 6 parts by weight of the antioxidant (RD) was put in a Banbury mixer and blended for 30 minutes at 150 ℃ and released.

그런 다음 가류제로서 유황 2.2중량부, 가류촉진제로서 N-시클로헥실-2-벤조티아졸설펜아미드(N-cyclohexyl-2-benzothiazolsulfenamide, CZ) 0.9중량부를 상기의 배합물에 첨가하고 160℃에서 20분 동안 가류하여 고무를 제조하였다.Then, 2.2 parts by weight of sulfur as a vulcanizing agent and 0.9 parts by weight of N-cyclohexyl-2-benzothiazolsulfenamide (CZ) as a vulcanization accelerator were added to the above formulation and 20 minutes at 160 ° C. Was vulcanized to produce a rubber.

상기에서 카본블랙은 BET값이 120∼160m2/g, DBP흡착량이 110∼160ml/100g인 것을 사용하였고, 실리카는 BET값이 150∼200m2/g이고, DBP흡착량이 240∼300ml/100g인 것을 사용하였다.In the carbon black, a BET value of 120 to 160 m 2 / g and a DBP adsorption amount of 110 to 160 ml / 100 g were used. Silica had a BET value of 150 to 200 m 2 / g and a DBP adsorption amount of 240 to 300 ml / 100 g. Was used.

하기의 표 1에 비교예 고무의 성분을 정리하여 나타내었다.Table 1 below shows the components of the rubber of the comparative example.

<실시예><Example>

천연고무(NR) 60중량부, 부타디엔 고무 40중량부로 이루어진 원료고무 100중량부에 대하여 카본블랙 57중량부, 실리카 5중량부, 실란커플링제(SI-69) 1.5중량부, 아연-2-에틸-헥사노에이트(ZEH) 3중량부, 공정오일(Aromatic-2) 6중량부, 스테 아린산 1.5중량부, 산화아연 3중량부, 노화방지제(RD) 6중량부를 밴버리 믹서에 넣고 150℃에서 30분 동안 배합한 후 방출하였다.57 parts by weight of carbon black, 5 parts by weight of silica, 1.5 parts by weight of silane coupling agent (SI-69), zinc-2-ethyl based on 100 parts by weight of the raw material rubber consisting of 60 parts by weight of natural rubber (NR) and 40 parts by weight of butadiene rubber 3 parts by weight of hexanoate (ZEH), 6 parts by weight of process oil (Aromatic-2), 1.5 parts by weight of stearic acid, 3 parts by weight of zinc oxide, and 6 parts by weight of antioxidant (RD) in a Banbury mixer at 150 ° C. Release for 30 minutes after compounding.

그런 다음 가류제로서 유황 2.2중량부, 가류촉진제로서 N-시클로헥실-2-벤조티아졸설펜아미드(N-cyclohexyl-2-benzothiazolsulfenamide, CZ) 0.9중량부를 상기의 배합물에 첨가하고 160℃에서 20분 동안 가류하여 고무를 제조하였다.Then, 2.2 parts by weight of sulfur as a vulcanizing agent and 0.9 parts by weight of N-cyclohexyl-2-benzothiazolsulfenamide (CZ) as a vulcanization accelerator were added to the above formulation and 20 minutes at 160 ° C. Was vulcanized to produce a rubber.

상기에서 카본블랙은 BET값이 120∼160m2/g, DBP흡착량이 110∼160ml/100g인 것을 사용하였고, 실리카는 BET값이 150∼200m2/g이고, DBP흡착량이 240∼300ml/100g인 것을 사용하였다. 또한 분산조제로 사용한 아연-2-에틸-헥사노에이트(ZEH)는 아연 함량이 8%, 실리카 함량이 33%인 것을 사용하였다. In the carbon black, a BET value of 120 to 160 m 2 / g and a DBP adsorption amount of 110 to 160 ml / 100 g were used. Silica had a BET value of 150 to 200 m 2 / g and a DBP adsorption amount of 240 to 300 ml / 100 g. Was used. In addition, zinc-2-ethyl-hexanoate (ZEH) used as a dispersing aid was used having a zinc content of 8% and a silica content of 33%.

하기의 표 1에 실시예 고무의 성분을 정리하여 나타내었다.Table 1 below shows the components of the rubber example.

표 1. 실시예 및 비교예 고무의 조성 Table 1. Compositions of Examples and Comparative Examples Rubber

항목Item 비교예Comparative example 실시예Example 천연고무Natural rubber 6060 6060 부타디엔 고무Butadiene rubber 4040 4040 카본블랙Carbon black 5757 5757 실리카Silica 55 55 실란커플링제Silane coupling agent 1.51.5 1.51.5 ZEHZEH -- 33 공정오일Process oil 66 66 스테아린산Stearic acid 1.51.5 1.51.5 산화아연Zinc oxide 33 33 노화방지제(RD)(1)Antioxidant (RD) (1) 66 66 가류제(유황)Vulcanizing (sulfur) 2.22.2 2.22.2 가류촉진제(CZ)Vulcanization accelerator (CZ) 0.90.9 0.90.9

(1)RD : 2,2,4-trimethyl-1,2-dihydroquinoline(1) RD: 2,2,4-trimethyl-1,2-dihydroquinoline

<시험예 1><Test Example 1>

상기 실시예 및 비교예 고무에 대하여 ASTM 관련 규정에 의해 인장물성(경도, 300%모듈러스, 인장강도, 신율), 스코치시간, 점도, 발열과 같은 물성을 측정하고 그 결과를 아래의 표 2에 나타내었다.Physical properties such as tensile properties (hardness, 300% modulus, tensile strength, elongation), scorch time, viscosity, and heat generation were measured according to ASTM-related regulations for the rubbers of Examples and Comparative Examples, and the results are shown in Table 2 below. It was.

표 2. 실시예 및 비교예 고무의 물성Table 2. Physical Properties of Examples and Comparative Examples Rubber

항목Item 비교예Comparative example 실시예Example 경도(Shore A)Shore A 67/7267/72 67/7167/71 300%모듈러스(kg/cm2)300% modulus (kg / cm 2 ) 130/170130/170 133/167133/167 인장강도(kg/cm2)Tensile Strength (kg / cm 2 ) 230/207230/207 227/205227/205 신율(%)Elongation (%) 492/366492/366 461/356461/356 스코치시간(분)Scorch time (minutes) 32.132.1 36.236.2 점도(100℃)Viscosity (100 ° C) 6666 5959 발열(℃)Fever (℃) 30.330.3 27.827.8

* 인장물성은 측정값은 초기/노화이고, 노화조건은 100℃에서 24시간 동안 방치하였다.* Tensile property is the initial value / aging, aging conditions were left at 100 ℃ for 24 hours.

* 인장 노화물성의 300%모듈러스, 인장강도는 초기 물성 대비 상승률이 낮을수록 우수하다.* 300% modulus of tensile aging, tensile strength is better the lower the rate of increase compared to the initial physical properties.

* 발열성능은 상승온도가 적을수록, 즉 수치가 낮을수록 우수하고, 점도(100℃)는 낮을수록 우수하다.* The exothermic performance is excellent at the lower temperature, that is, the lower the value, and the better the viscosity (100 ℃).

* 스코치 시간은 길수록 공정성에 유리하다.* Longer scorch time favors fairness.

<시험예 2><Test Example 2>

상기 실시예 및 비교예에서 제조한 고무에 대하여 고무 압출물 표면온도, 고무 압출물 내부온도를 측정하고 그 결과를 아래의 표 3에 나타내었다.The rubber extrudate surface temperature and the rubber extrudate internal temperature of the rubber prepared in Examples and Comparative Examples were measured and the results are shown in Table 3 below.

또한 상기 실시예 및 비교예에서 제조한 고무를 트레드로 하여 315/80R22.5 규격의 실차에 적용하고, 내구력(트레드의 파단시간), 실차 마모지수를 측정하고 그 결과를 아래의 표 3에 나타내었다.In addition, the rubber prepared in Examples and Comparative Examples was applied to a real vehicle of the 315 / 80R22.5 standard as a tread, and the durability (break time of the tread) and the actual vehicle wear index were measured and the results are shown in Table 3 below. It was.

표 3. 실시예 및 비교예 고무의 특성Table 3. Properties of Examples and Comparative Examples Rubber

항목Item 비교예Comparative example 실시예Example 고무 압출물 표면온도(℃)Rubber Extruded Surface Temperature (℃) 139.0139.0 132.0132.0 고무 압출물 내부온도(℃)Rubber Extruded Internal Temperature (℃) 146.0146.0 139.0139.0 내구력(파단시간)Durability (break time) 64시간 09분64 hours 09 minutes 65시간 50분65 hours 50 minutes 실차 마모지수Actual vehicle wear index 100100 103103

* 내구력은 유럽규정의 속도 내구력 측정시험인 ECER-54에 의해 트레드가 파단되는 시간을 측정한 값으로 수치(파단시간)가 높을수록 우수함을 의미한다.* Durability is a measure of the time that a tread breaks by ECER-54, the speed endurance test of the European standard. The higher the value (break time), the better.

* 실시예의 실차 마모지수는 비교예의 측정값을 100으로 하였을 때의 환산한 측정값으로 수치가 높을수록 우수함을 의미한다.* Actual vehicle wear index of Examples is measured value converted to the measured value of the comparative example to 100 means that the higher the value is better.

상기 시험예 1의 결과에서처럼 분산조제를 적용한 본 발명의 실시예 고무는 분산조제를 적용하지 않은 비교예의 고무와 대비시, 동등 수준 이상의 물성을 가지고 있으며, 특히 발열특성이 우수하고, 점도가 감소되어 공정성이 향상되었음을 알 수 있다.Rubber of the present invention to which the dispersing aid is applied as in the result of Test Example 1, compared with the rubber of the comparative example without the dispersing aid, has a physical property equivalent or more, in particular, the exothermic property is excellent, the viscosity is reduced It can be seen that the fairness is improved.

또한 시험예 2의 결과에서처럼 분산조제를 첨가한 실시예의 고무는 분산조제를 사용하지 않은 비교예 고무에 비해 스코치 시간이 안정화됨으로써 내구력이 향상되었으며, 마모특성은 동등 수준 이상임을 알 수 있다.In addition, as in the result of Test Example 2, the rubber of the example to which the dispersion aid was added, compared with the rubber of the comparative example without the dispersion aid stabilized scorch time is improved durability, and it can be seen that the wear characteristics are equal to or more than.

상술한 바와 같이, 본 발명의 바람직한 실시예를 참조하여 설명하였지만 해 당 기술 분야의 숙련된 당업자라면 하기의 특허청구범위에 기재된 본 발명의 사상 및 영역으로부터 벗어나지 않는 범위 내에서 본 발명을 다양하게 수정 및 변경시킬 수 있음을 이해할 수 있을 것이다. As described above, although described with reference to the preferred embodiment of the present invention, those skilled in the art will be variously modified without departing from the spirit and scope of the invention described in the claims below. And can be changed.

Claims (3)

타이어 트레드 고무조성물에 있어서,In the tire tread rubber composition, 원료고무 100중량부에 대하여 아연-2-에틸-헥사노에이트 1∼5중량부 포함함을 특징으로 하는 타이어 트레드 고무조성물.A tire tread rubber composition comprising 1 to 5 parts by weight of zinc-2-ethyl-hexanoate based on 100 parts by weight of raw rubber. 제1항에 있어서, 아연-2-에틸-헥사노에이트는 아연 함량이 6∼10%, 실리카 함량이 30∼35% 임을 특징으로 하는 타이어 트레드 고무조성물.The tire tread rubber composition according to claim 1, wherein zinc-2-ethyl-hexanoate has a zinc content of 6 to 10% and a silica content of 30 to 35%. 특허청구범위 제1항 또는 제2항의 고무조성물로 이루어진 트레드를 포함하는 타이어.A tire comprising a tread made of the rubber composition of claim 1.
KR1020050054188A 2005-06-22 2005-06-22 Tire tread rubber composition for improving good extrusion KR100635608B1 (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20190122448A (en) * 2018-04-20 2019-10-30 주식회사 미래에스아이 Styrene-butadiene rubber compound with high contents of silica and the process thereof

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20190122448A (en) * 2018-04-20 2019-10-30 주식회사 미래에스아이 Styrene-butadiene rubber compound with high contents of silica and the process thereof
KR102070987B1 (en) * 2018-04-20 2020-01-29 주식회사 미래에스아이 Styrene-butadiene rubber compound with high contents of silica and the process thereof

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