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KR20030030592A - Tread Rubber composition improved wet traction - Google Patents

Tread Rubber composition improved wet traction Download PDF

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Publication number
KR20030030592A
KR20030030592A KR1020010062796A KR20010062796A KR20030030592A KR 20030030592 A KR20030030592 A KR 20030030592A KR 1020010062796 A KR1020010062796 A KR 1020010062796A KR 20010062796 A KR20010062796 A KR 20010062796A KR 20030030592 A KR20030030592 A KR 20030030592A
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rubber
phr
rubber composition
tread rubber
natural rubber
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KR1020010062796A
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KR100426067B1 (en
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이화우
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금호산업 주식회사
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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L7/00Compositions of natural rubber
    • 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
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L13/00Compositions of rubbers containing carboxyl groups
    • C08L13/02Latex

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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)
  • Tires In General (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

PURPOSE: Provided is a tread rubber composition which uses, as raw rubber, a mixture of liquid butadiene rubber having carboxyl group and natural rubber and improves a braking capability of tire. CONSTITUTION: The tread rubber composition uses a mixture of 70-98 phr of epoxidized natural rubber(ENR) and 2-30 phr of carboxyl terminated reactive liquid polybutadiene(CT-RLP) as a raw rubber. The content of epoxy group of the epoxidized natural rubber(ENR) is 10-60 mol%. The number of carboxyl group of carboxyl terminated reactive liquid polybutadiene is 3-10. The tread rubber composition can retain an anti-wear at least equivalent to existing tread rubber composition.

Description

제동성이 향상된 트레드 고무조성물{Tread Rubber composition improved wet traction}Tread Rubber composition improved wet traction

본 발명은 제동성이 향상된 트레드 고무조성물에 관한 것으로서 보다 상세하게는 공지의 트레드 고무조성물에 있어서, 천연고무의 불포화기에 에폭시기를 도입한 에폭시화 천연고무(ENR) 70∼98 phr, 카르복실기를 도입한 카르복실화 액상 부타디엔 고무(CT-RLP) 2∼30 phr의 혼합물을 원료고무로 사용하는 것을 특징으로 한다.The present invention relates to a tread rubber composition with improved braking properties. More specifically, in a known tread rubber composition, 70 to 98 phr of epoxidized natural rubber (ENR) in which an epoxy group is introduced into an unsaturated group of a natural rubber, and a carboxyl group are introduced. It is characterized by using a mixture of carboxylated liquid butadiene rubber (CT-RLP) 2 to 30 phr as raw material rubber.

자동차용 타이어의 요구성능은 타이어의 사용용도 및 부위에 따라서 크게 다르다. 특히 노면과 직접적으로 접촉하는 트레드 고무는 내마모성능, 젖은 노면에서의 제동력 및 크랙저항성 등의 많은 요구특성이 있다.The required performance of automobile tires varies greatly depending on the use and parts of the tire. In particular, the tread rubber that is in direct contact with the road surface has many demanding characteristics such as wear resistance, braking force on a wet road surface, and crack resistance.

이러한 요구특성중 내마모성능은 타이어의 내구성과 직결되어 타이어 사용에 있어서, 경제적인 연관성이 커서 소비자의 요구특성이 크며, 안전성과 관련있는 타이어의 제동성능은 차량의 제동에 밀접한 관련이 있어 소비자의 주요한 요구특성 중의 하나이다.Among these required characteristics, abrasion resistance is directly related to tire durability, and the economical relationship of tire use is large, and thus the consumer's required characteristic is large, and the braking performance of tires related to safety is closely related to vehicle braking. One of the required characteristics.

종래에는 트레드 고무의 제동성을 향상시키기 위하여 원료고무로 천연고무와 스티렌-부타디엔 유화중합체(E-SBR)의 혼합물을 사용하여 제동성을 향상시켰으나 스티렌-부타디엔 유화중합체는 천연고무에 비하여 탄성이 적고 반복적인 하중을 주었을 때 발열이 커서 타이어 트레드 고무에 사용하여 주행시 트레드 및 벨트부위의 분리를 유발할 가능성이 있으며 내마모성능도 감소하는 단점이 있다.Conventionally, in order to improve the braking property of the tread rubber, a mixture of natural rubber and styrene-butadiene emulsion (E-SBR) is used as the raw material rubber to improve the braking property, but the styrene-butadiene emulsion is less elastic than the natural rubber. When repeated loads are applied, the heat generation is large and may be used for the tire tread rubber, which may cause separation of the tread and the belt part while driving, and also has the disadvantage of reducing the wear resistance.

최근에는 상기와 같은 문제점을 해결하기 위해 원료고무를 일반적인 천연고무 대신에 에폭시가 함유된 에폭시화 천연고무를 사용하여 젖은 노면에서의 제동성을 향상시키고, 내마모성을 향상시키기 위해 보강충진제인 카본블랙의 사용량을 증가시키는 한편, 카본블랙의 사용량에 따른 점도의 증가로 인해 압출공정이 불량해지는 단점을 해소하기 위해 점도가 낮은 액상 이소프렌 고무를 사용하여 공정성을 개선시키지만 이때에는 고무배합물의 물성이 하락하는 문제가 있다.Recently, in order to solve the problems described above, carbon black, which is a reinforcing filler, is used to improve braking property on wet roads and improve wear resistance by using epoxidized natural rubber containing epoxy instead of general natural rubber. In order to solve the disadvantage that the extrusion process is poor due to the increase in the viscosity of the carbon black, the use of low-viscosity liquid isoprene rubber is used to improve the processability, but the physical properties of the rubber compound are deteriorated. There is.

본 발명은 상기와 같은 문제점을 해결하기 위해 노력하던중 제동성을 향상시키기 위해 에폭시화 천연고무 및 가공성 및 물성향상을 위해 카르복실기를 도입한 액상 부타디엔 고무의 혼합물을 원료고무로 사용시 종래 트레드 고무조성물과 비교하여 동등 수준 이상의 물성을 가지며, 제동성을 향상시킬 수 있음을 알게 되었다.The present invention is a conventional tread rubber composition when using a mixture of epoxidized natural rubber and a liquid butadiene rubber incorporating a carboxyl group to improve the processability and physical properties to improve the braking properties while trying to solve the problems as described above In comparison, it has been found that they have more than equivalent physical properties and can improve braking properties.

따라서 본 발명은 에폭시화 천연고무 및 카르복실기를 도입한 액상 부타디엔 고무의 혼합물을 원료고무로 사용하여 제동성을 향상시키는 트레드 고무조성물의 제공을 목적으로 한다.Accordingly, an object of the present invention is to provide a tread rubber composition which improves braking property by using a mixture of epoxidized natural rubber and liquid butadiene rubber having a carboxyl group as a raw material rubber.

본 발명의 제동성이 향상된 트레드 고무조성물은 공지의 트레드 고무조성물에 있어서, 천연고무의 불포화기에 에폭시기를 도입한 에폭시화 천연고무 (Epoxidized natural rubber, ENR) 70∼98 phr, 카르복실기를 도입한 카르복실화 액상 부타디엔 고무(Carboxyl terminated reactive liquid polybutadiene, CT-RLP) 2∼30 phr의 혼합물을 원료고무로 사용하는 것을 특징으로 한다.The tread rubber composition of which the braking property of the present invention is improved is 70-98 phr of epoxidized natural rubber (ENR) in which an epoxy group is introduced into an unsaturated group of natural rubber, and a carboxyl group having a carboxyl group. Carboxyl terminated reactive liquid polybutadiene (CT-RLP) is characterized in that a mixture of 2 to 30 phr is used as a raw material rubber.

상기에서 에폭시화 천연고무는 천연고무의 주쇄에 에폭시기가 부가되어 유리전이온도(Glass transition temperature, Tg)가 상승하는 특성이 있다. 본 발명에서는 에폭시화 천연고무의 에폭시기 함량은 10∼60mol%인 것을 사용하는데 에폭시기가 10mol% 미만 사용하면 유리전이온도가 내려가서 제동성능의 향상이 미미하고, 60mol% 초과 사용하면 유리전이온도가 너무 높아져서 내한성능이 하락하고 물성도 저하되는 단점이 있어 에폭시화 천연고무의 에폭시기 함량은 10∼60mol% 유지하는 것이 좋다.The epoxidized natural rubber is characterized in that the glass transition temperature (Tg) is increased by adding an epoxy group to the main chain of the natural rubber. In the present invention, the epoxy group content of the epoxidized natural rubber is 10 to 60 mol%, but when the epoxy group is used below 10 mol%, the glass transition temperature is lowered and the braking performance is insignificant. It has a disadvantage in that the cold resistance performance is lowered and the physical properties are also lowered, so the epoxy group content of the epoxidized natural rubber is preferably maintained at 10 to 60 mol%.

또한 원료고무중 에폭시화 천연고무를 70 phr 미만 사용하면 제동성능이 하락하는 문제가 있고, 98 phr 초과 사용하면 제동성능은 향상되나 고무배합물의 물성이 하락하는 문제가 있어 원료고무중 에폭시화 천연고무는 70∼98 phr 유지하는 것이 좋다.In addition, if the epoxidized natural rubber is less than 70 phr, the braking performance is reduced. If it is more than 98 phr, the braking performance is improved, but the physical properties of the rubber compound are deteriorated. It is recommended to keep 70-98 phr.

한편 에폭시화 천연고무의 내마모성을 개선하기 위해서 보강성 충진제인 카본블랙을 많이 사용하지만 점도가 높아져서 공정성이 하락하는 문제가 있어 이를 개선하기 위해 액상 이소프렌 고무(Liquid isoprene, LIR)를 사용함으로써 공정성을 향상시키지만 물성이 하락하는 문제가 있다. 본 발명에서는 이러한 액상 이소프렌 고무의 단점을 해결하기 위해 다양한 노력을 하던중 카르복실기(-COOH)가 도입된 액상 카르복실화 부타디엔 고무를 에폭시화 천연고무와 혼합하여 원료고무로 사용하면 공정성이 개선되면서도 카르복실기와 에폭시기의 반응에 의해 탄성이 증가하고 물성이 향상됨을 알게 되었다.In order to improve the abrasion resistance of epoxidized natural rubber, carbon black, a reinforcing filler, is used a lot, but there is a problem that the processability decreases due to the increase in viscosity. Therefore, liquid isoprene (LIR) is used to improve the processability. But there is a problem that the physical properties fall. In the present invention, while making various efforts to solve the disadvantages of the liquid isoprene rubber, when the liquid carboxylated butadiene rubber in which the carboxyl group (-COOH) is introduced is mixed with the epoxidized natural rubber and used as the raw material rubber, the carboxyl group is improved. It was found that the elasticity is increased and the physical properties are improved by the reaction of the epoxy group.

본 발명에서 원료고무 중 카르복실화 액상 부타디엔 고무를 2 phr 미만 사용하면 물성이 하락하는 문제가 있고, 30 phr 초과 사용하면 공정성이 하락하는 문제가 있어 원료고무중 카르복실화 액상 부타디엔 고무는 2∼70 phr 유지한다.In the present invention, when the carboxylated liquid butadiene rubber in the raw material rubber is less than 2 phr, there is a problem that the physical properties are deteriorated. Keep 70 phr.

또한 카르복실화 액상 부타디엔 고무의 카르복실기 함량은 관능기의 수가 3∼10인 것을 사용하는데 카르복실기 수가 3 미만이면 본원 발명의 목적인 제동성능이 감소하는 문제가 이고, 카르복실기 수가 10 초과 사용하면 신율 등이 하락하는 문제가 있어 원료고무중 카르복실화 액상 부타디엔 고무의 카르복실기 함량은 3∼10 유지한다.In addition, the carboxyl group content of the carboxylated liquid butadiene rubber has a functional group number of 3 to 10. If the number of carboxyl groups is less than 3, there is a problem in that the braking performance of the present invention is reduced. There is a problem that the carboxyl group content of the carboxylated liquid butadiene rubber in the raw material rubber is maintained at 3 to 10.

이하 본 발명을 다음의 비교예, 실시예 및 시험예에 의하여 설명하고자 한다. 그러나 이들이 본 발명의 권리범위를 한정하는 것은 아니다.Hereinafter, the present invention will be described by the following comparative examples, examples and test examples. However, these do not limit the scope of the present invention.

<비교예>Comparative Example

천연고무 100 phr을 원료고무로 하고, 통상적으로 사용하는 타이어 첨가제인 카본블랙 60 phr, 아연화 5 phr, 스테아린산 2 phr, 노화방지제 2 phr, 공정유 3 phr, 황 2 phr 및 촉진제 1 phr을 혼합하여 155℃의 온도에서 30분 동안 가류한 후 방출하여 고무시편을 제조하였다. 아래의 표 1에 고무조성물의 배합비를 나타내었다.100 phr of natural rubber is used as a raw material, and 60 phr of carbon black which is a commonly used tire additive, 5 phr of galvanized, 2 phr of stearic acid, 2 phr of antioxidant, 3 phr of process oil, 2 phr of sulfur and 1 phr of accelerator After vulcanization at a temperature of 155 ℃ for 30 minutes to release to prepare a rubber specimen. Table 1 below shows the mixing ratio of the rubber composition.

<실시예 1><Example 1>

에폭시기 함량이 25 mol%인 에폭시화 천연고무(ENR) 100 phr을 원료고무로 하고, 통상적으로 사용하는 타이어 첨가제인 카본블랙 60 phr, 아연화 5 phr, 스테아린산 2 phr, 노화방지제 2 phr, 공정유 3 phr, 황 2 phr 및 촉진제 1 phr을 혼합하여 155℃의 온도에서 30분 동안 가류한 후 방출하여 고무시편을 제조하였다. 아래의 표 1에 고무조성물의 배합비를 나타내었다.100 phr of epoxidized natural rubber (ENR) having an epoxy group content of 25 mol% is used as a raw material, 60 phr of carbon black which is a commonly used tire additive, 5 phr of zinc, 5 phr of stearic acid, 2 phr of an antioxidant, process oil 3 phr, sulfur 2 phr, and accelerator 1 phr were mixed and vulcanized at a temperature of 155 ° C. for 30 minutes before release to prepare a rubber specimen. Table 1 below shows the mixing ratio of the rubber composition.

<실시예 2><Example 2>

에폭시기 함량이 25 mol%인 에폭시화 천연고무(ENR) 90 phr 및 액상 이소프렌 고무(LIR) 10 phr의 혼합물을 원료고무로 사용하는 것을 제외하고는 상기 실시예 1과 동일한 배합비 및 방법을 이용하여 고무시편을 제조하였다.Rubber was prepared using the same blending ratio and method as in Example 1, except that a mixture of 90 phr of epoxidized natural rubber (ENR) and 10 phr of liquid isoprene rubber (LIR) having an epoxy group content of 25 mol% was used. Specimen was prepared.

<실시예 3><Example 3>

에폭시기 함량이 25 mol%인 에폭시화 천연고무(ENR) 90 phr 및 카르복실기가도입된 액상의 카르복실화 부다디엔 고무(CT-RLP) 10 phr의 혼합물을 원료고무로 사용하는 것을 제외하고는 상기 실시예 1과 동일한 배합비 및 방법을 이용하여 고무시편을 제조하였다.The above procedure was carried out except that a mixture of 90 phr of epoxidized natural rubber (ENR) having an epoxy group content of 25 mol% and 10 phr of a liquid carboxylated butadiene rubber (CT-RLP) in which a carboxyl group was introduced was used. Rubber specimens were prepared using the same mixing ratio and method as in Example 1.

표 1. 비교예 및 실시예의 고무조성물 배합비(단위 : phr)Table 1. Mixing ratio of rubber composition of Comparative Example and Example (unit: phr)

항 목Item 비교예Comparative example 실시예 1Example 1 실시예 2Example 2 실시예 3Example 3 원료고무Raw material rubber 천연고무Natural rubber 100100 -- -- -- ENRENR -- 100100 9090 9090 LIRLIR -- -- 1010 -- CT-RLPCT-RLP -- -- -- 1010 카본블랙Carbon black 6060 6060 6060 6060 아연화Zincification 55 55 55 55 스테아린산Stearic acid 22 22 22 22 노화방지제Anti-aging 1One 1One 1One 1One 공정유Process oil 33 33 33 33 sulfur 22 22 22 22 촉진제accelerant 1One 1One 1One 1One

<시험예><Test Example>

상기 비교예 및 실시예로부터 제조한 고무시편에 대하여 점도, 제동성능 및 내마모성의 물성을 공지의 표준방법에 의해 측정하여 그 결과를 아래의 표 2에 나타내었다.The rubber, rubber, and abrasion resistance of the rubber specimens prepared from Comparative Examples and Examples were measured by a standard method, and the results are shown in Table 2 below.

표 2. 비교예 및 실시예 고무시편의 물성측정 결과Table 2. Measurement results of the rubber specimens of Comparative Examples and Examples

항 목Item 비교예Comparative example 실시예 1Example 1 실시예 2Example 2 실시예 3Example 3 점도Viscosity 100100 9393 112112 110110 제동성능Braking performance 100100 140140 138138 145145 내마모성Wear resistance 100100 9090 8080 9999

이때 각 실시예의 수치는 비교예를 100으로 기준하여 환산한 값으로 수치가 높을수록 양호함을 의미한다.At this time, the numerical value of each Example is a value converted on the basis of the comparative example 100 means that the higher the value.

상기 표 2에서처럼 본 발명의 에폭시화 천연고무 및 카르복실화 부다디엔 고무를 원료고무로 사용한 트레드 고무조성물은 천연고무 단독 또는 천연고무와 액상이소프렌 고무의 혼합물을 원료고무로 사용한 종래의 트레드 고무조성물과 비교시 내마모성은 동등 수준 이상을 유지하는 한편 안전성과 관련있는 제동성능이 향상하여 젖은 노면에서도 제동성능을 향상시킬 수 있다.As shown in Table 2, the tread rubber composition using the epoxidized natural rubber and carboxylated butadiene rubber of the present invention as the raw material rubber is a conventional tread rubber composition using only natural rubber or a mixture of natural rubber and liquid isoprene rubber as the raw material rubber. In comparison, abrasion resistance can be maintained at an equivalent level or higher, and the braking performance related to safety can be improved to improve braking performance even on wet roads.

Claims (3)

공지의 트레드 고무조성물에 있어서, 에폭시화 천연고무(ENR) 70∼98 phr, 카르복실화 액상 부타디엔 고무(CT-RLP) 2∼30 phr의 혼합물을 원료고무로 사용하는 것을 특징으로 하는 트레드 고무조성물In a known tread rubber composition, a tread rubber composition using a mixture of 70 to 98 phr of epoxidized natural rubber (ENR) and 2 to 30 phr of carboxylated liquid butadiene rubber (CT-RLP) as a raw material rubber 제 1항에 있어서, 에폭시화 천연고무의 에폭시기 함량은 10∼60mol% 임을 특징으로 하는 트레드 고무조성물The tread rubber composition according to claim 1, wherein the epoxy group content of the epoxidized natural rubber is 10 to 60 mol%. 제 1항에 있어서, 카르복실화 액상 부타디엔 고무의 카르복실기 함량은 관능기의 수가 3∼10 임을 특징으로 하는 트레드 고무조성물The tread rubber composition according to claim 1, wherein the carboxyl group content of the carboxylated liquid butadiene rubber is 3 to 10 functional groups.
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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100682321B1 (en) * 2004-07-19 2007-02-15 김대건 An extruding machine for a waste matter
US20150299435A1 (en) * 2012-12-17 2015-10-22 Compagnie Generale Des Etablissements Michelin Tire comprising a rubber composition comprising an epoxide elastomer crosslinked with a polycarboxylic acid
US10421858B2 (en) 2014-06-18 2019-09-24 Compagnie Generale Des Etablissements Michelin Rubber composition comprising an epoxide elastomer cross-linked by a polycarboxylic acid

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3859239A (en) * 1971-07-14 1975-01-07 Gen Tire & Rubber Co Adhesive for bonding rubber to steel
US5396940A (en) * 1993-09-17 1995-03-14 The Goodyear Tire & Rubber Company Sulfur cured rubber composition containing epoxidized natural rubber and silica filler
JP2912845B2 (en) * 1994-04-20 1999-06-28 住友ゴム工業株式会社 Rubber composition for tire
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
KR100222912B1 (en) * 1997-06-19 1999-10-01 신형인 Mixed rubber compositions

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100682321B1 (en) * 2004-07-19 2007-02-15 김대건 An extruding machine for a waste matter
US20150299435A1 (en) * 2012-12-17 2015-10-22 Compagnie Generale Des Etablissements Michelin Tire comprising a rubber composition comprising an epoxide elastomer crosslinked with a polycarboxylic acid
US10421858B2 (en) 2014-06-18 2019-09-24 Compagnie Generale Des Etablissements Michelin Rubber composition comprising an epoxide elastomer cross-linked by a polycarboxylic acid

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