JPH0637582B2 - Carbon black for tire tread rubber - Google Patents

Carbon black for tire tread rubber

Info

Publication number
JPH0637582B2
JPH0637582B2 JP63182378A JP18237888A JPH0637582B2 JP H0637582 B2 JPH0637582 B2 JP H0637582B2 JP 63182378 A JP63182378 A JP 63182378A JP 18237888 A JP18237888 A JP 18237888A JP H0637582 B2 JPH0637582 B2 JP H0637582B2
Authority
JP
Japan
Prior art keywords
carbon black
rubber
oil absorption
surface area
tire tread
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
JP63182378A
Other languages
Japanese (ja)
Other versions
JPH0232136A (en
Inventor
泰治 吉井
伸司 味曽野
仁志 植
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Tokai Carbon Co Ltd
Original Assignee
Tokai Carbon Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Tokai Carbon Co Ltd filed Critical Tokai Carbon Co Ltd
Priority to JP63182378A priority Critical patent/JPH0637582B2/en
Priority to KR1019890009848A priority patent/KR930002554B1/en
Priority to FR8909601A priority patent/FR2634491B1/en
Publication of JPH0232136A publication Critical patent/JPH0232136A/en
Priority to US07/759,378 priority patent/US5198205A/en
Publication of JPH0637582B2 publication Critical patent/JPH0637582B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09CTREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK  ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
    • C09C1/00Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
    • C09C1/44Carbon
    • C09C1/48Carbon black
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09CTREATMENT OF INORGANIC MATERIALS, OTHER THAN FIBROUS FILLERS, TO ENHANCE THEIR PIGMENTING OR FILLING PROPERTIES ; PREPARATION OF CARBON BLACK  ; PREPARATION OF INORGANIC MATERIALS WHICH ARE NO SINGLE CHEMICAL COMPOUNDS AND WHICH ARE MAINLY USED AS PIGMENTS OR FILLERS
    • C09C1/00Treatment of specific inorganic materials other than fibrous fillers; Preparation of carbon black
    • C09C1/44Carbon
    • C09C1/48Carbon black
    • C09C1/50Furnace black ; Preparation thereof
    • 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

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Pigments, Carbon Blacks, Or Wood Stains (AREA)
  • Tires In General (AREA)

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は、ゴム成分に高度の耐摩耗性と相対的に低位の
発熱性を付与することができるタイヤトレッドゴム用カ
ーボンブラックに関する。
Description: TECHNICAL FIELD The present invention relates to a carbon black for a tire tread rubber capable of imparting a rubber component with a high degree of wear resistance and a relatively low level of heat generation.

〔従来の技術〕[Conventional technology]

カーボンブラックによるゴムの補強性能は、従来からそ
の比表面積(粒子径)やストラクチャーが支配的な因子
として考えられており、具備特性に応じた多様な品種が
ある。そして、ゴム成分との配合にあたっては、用途部
材に適合する品種特性のカーボンブラックが選択使用さ
れている。例えばタイヤトレッド部のような苛酷な走行
条件下で、高度の耐摩耗性が要求されるゴム部材には、
N110、N220などのハード系カーボンブラックが
適用されている。
It has been conventionally considered that the specific surface area (particle diameter) and the structure of the reinforcing performance of rubber with carbon black are the dominant factors, and there are various types according to the characteristics of the rubber. When blending with the rubber component, carbon black having a variety of characteristics suitable for the intended member is selectively used. For example, for rubber members that require a high degree of wear resistance under severe driving conditions such as tire treads,
Hard carbon black such as N110 and N220 is applied.

しかし近年タイヤ走行の高苛酷化により、タイヤトレッ
ド部に要求される性能も高度化し、とくに高耐摩耗性と
低発熱性とを兼ね備えることが重要とされている。
However, in recent years, due to the severer tire running, the performance required for the tire tread has become more sophisticated, and it is particularly important to have both high wear resistance and low heat buildup.

一般に、カーボンブラックの比表面積やストラクチャー
が大きい程耐摩耗性は増大するが、反面、発熱性が高く
なり、両特性には二律背反的関係がある。従ってゴム組
成物に高耐摩耗性と低発熱性とを同時に付与することは
極めて困難である。
Generally, the larger the specific surface area and the structure of carbon black, the more the abrasion resistance increases, but on the other hand, the heat generation property increases, and both characteristics have a trade-off relationship. Therefore, it is extremely difficult to impart high abrasion resistance and low heat buildup to the rubber composition at the same time.

この問題を解決するために、特定の性質を有するカーボ
ンブラックを適用する試みが種々提案されている(特公
昭53-34149号、特開昭63-112638号など)。
In order to solve this problem, various attempts to apply carbon black having specific properties have been proposed (Japanese Patent Publication No. 53-34149, Japanese Patent Publication No. 63-112638, etc.).

〔発明が解決しようとする課題〕[Problems to be Solved by the Invention]

しかし、従来提案されている選択的特性のカーボンブラ
ックを配合したゴム組成物は、未だ耐摩耗性と発熱性と
を良好なレベルに保有させるには不充分な面があり、一
層の改良が要望されている。
However, conventionally proposed rubber compositions containing carbon black having selective properties are still insufficient to retain wear resistance and heat buildup at good levels, and further improvement is desired. Has been done.

本発明は、上記の問題点を解消する目的で従来技術とは
別異な角度から研究を重ねた結果、一定のストラクチャ
ー水準をもつアグリゲートにおいて相対的に大きな凝集
体空隙を有するカーボンブラックをゴム成分に配合する
と背反ゴム性能(高耐摩耗性と低発熱性の併有)が効果
的に進行するとの知見を得て開発に至ったものである。
The present invention has conducted research from a different angle from the prior art for the purpose of solving the above-mentioned problems, and as a result, carbon black having relatively large aggregate voids in an aggregate having a certain structure level is used as a rubber component. It was developed based on the knowledge that anti-rubber performance (having both high abrasion resistance and low heat build-up) effectively progresses when compounded in.

〔課題を解決するための手段〕[Means for Solving the Problems]

すなわち、本発明により提供されるタイヤトレッドゴム
用カーボンブラックは、窒素吸着比表面積(NSA)
が60〜160m2/g、DBP吸油量が90〜150m/100
gのバード系領域に属し、かつ凝集体空隙容積Vp(m
/g)が〔0.00976×DBP吸油量−0.0358〕式によ
り算出される値以上の選択的特性を有することを特徴と
する。
That is, the carbon black for tire tread rubber provided by the present invention has a nitrogen adsorption specific surface area (N 2 SA).
Is 60 to 160 m 2 / g, DBP oil absorption is 90 to 150 m / 100
g of the bird-type region and the aggregate void volume Vp (m
/ G) has a selective characteristic of not less than the value calculated by the formula [0.00976 × DBP oil absorption-0.0358].

上記カーボンブラックの特性項目のうち、窒素吸着比表
面積(NSA)が60〜160m2/gの粒子範囲および
DBP吸油量90〜150m/100gのストラクチャー範囲
は通常品種のハード系領域に属し、配合ゴムに高度の耐
摩耗性を付与するための前提要件となる。この窒素吸着
比表面積(NSA)が60m2/g未満となり、DBP吸油
量が90m/100gを下廻るとタイヤトレッドとして耐
え得る高耐摩耗性を付与することができなくなる。ま
た、窒素吸着比表面積(NSA)が160m2/gを越える
場合には、ゴム成分への分散が悪化して耐摩耗性の向上
を阻害し、同時に発熱性の増大を招く。他方、DBP吸
油量が150m/100gを上廻るとアイススキッド性能が
低下するため好ましくない。
Among the characteristic items of the above carbon black, the range of particles having a nitrogen adsorption specific surface area (N 2 SA) of 60 to 160 m 2 / g and the structure range of the DBP oil absorption amount of 90 to 150 m / 100 g belong to the hard type region of a normal variety, It is a prerequisite for imparting a high degree of wear resistance to compounded rubber. When the nitrogen adsorption specific surface area (N 2 SA) is less than 60 m 2 / g and the DBP oil absorption amount is less than 90 m / 100 g, it becomes impossible to impart high wear resistance that the tire tread can withstand. Further, when the nitrogen adsorption specific surface area (N 2 SA) exceeds 160 m 2 / g, the dispersion in the rubber component is deteriorated and the abrasion resistance is hindered from being improved, and at the same time, the exothermic property is increased. On the other hand, if the DBP oil absorption exceeds 150 m / 100 g, the ice skid performance deteriorates, which is not preferable.

〔0.00976×DBP吸油量−0.0358〕式により導き出さ
れる凝集体空隙容積Vp(m/g)に関する選択特性
は、本発明を構成するカーボンブラックが有する高度に
ストラクチャーが発達した特有のアグリゲート構造を示
すもので、従来の同等品種のカーボンブラックに比べ異
方性が大きいことによって特長づけられる。そして、凝
集体空隙容積Vp(m/g)が上式により算出させる
値以上であるカーボンブラックは、異方性が大きい特有
のアグリゲート構造がゴム成分との配合過程で相互作用
を効率よく改善する機能を営み、この作用を介して窒素
吸着比表面積およびDBP吸油量が同等水準にある従来
品種のカーボンブラック配合時と同等の低発熱性を維持
しながら相対的に高度の耐摩耗性を付与することが可能
となる。
The selective property regarding the aggregate void volume Vp (m / g) derived by the formula [0.00976 × DBP oil absorption-0.0358] shows the highly aggregated and unique aggregate structure of the carbon black constituting the present invention. It is characterized by its greater anisotropy than conventional equivalent types of carbon black. Carbon black having an aggregate void volume Vp (m / g) equal to or greater than the value calculated by the above formula has a unique anisotropy structure with large anisotropy, which effectively improves the interaction with the rubber component during the compounding process. This function provides a relatively high degree of wear resistance while maintaining the same low heat buildup as when blending carbon black of a conventional product with a nitrogen adsorption specific surface area and DBP oil absorption at the same level. It becomes possible to do.

本発明に適用されるカーボンブラックの各特性値は、下
記の測定方法によって得られる値とする。
Each characteristic value of carbon black applied to the present invention is a value obtained by the following measuring method.

(1)窒素吸着比表面積(NSA) ASTM D3037−78“Standard Methods of Te
sting Carbon Black Surface Area by Nitrogen Adsorp
tion”Method Bによる。
(1) a nitrogen adsorption specific surface area (N 2 SA) ASTM D3037-78 " Standard Methods of Te
sting Carbon Black Surface Area by Nitrogen Adsorp
tion ”by Method B.

この方法で測定したIRB#5の窒素吸着比表面積(N
SA)は、80.3m2/gとなる。
IRB # 5 nitrogen adsorption specific surface area (N
2 SA) is 80.3 m 2 / g.

(2)DBP吸油量 JIS K6221(1975)「ゴム用カーボンブラックの試験
方法」6・1・2項の吸油量A法によって得られた値と
する。
(2) DBP oil absorption amount It is the value obtained by the oil absorption amount A method of JIS K6221 (1975) "Testing method of carbon black for rubber", 6.1.2.

(3)凝集体空隙容積Vp(m/g) JIS K6221(1985)「乾燥試料の作り方」に従って乾
燥処理したカーボンブラック(粒度250〜500μm造粒
品)を試料として、水銀ポロシメーター(マイクロメリ
ティクス社製、PORE SIZER 9300)を用いて凝集体空隙
径を測定し、次式により得られる凝集体空隙径0.006〜
7.2μまでの空隙径の累積容積を凝集体空隙容積Vpと
する。
(3) Aggregate void volume Vp (m / g) A mercury porosimeter (Micromeritics Co., Ltd.) was used as a sample of carbon black (granulated product having a particle size of 250 to 500 μm) dried according to JIS K6221 (1985) “How to prepare a dried sample”. Manufactured by PORE SIZER 9300) to measure the pore size of the aggregate, and obtain the aggregate void size of 0.006 ~
The cumulative volume of void diameters up to 7.2μ is defined as the aggregate void volume Vp.

但し、上式において、Xは25psiでの指示値(p
F)、Xは終点30,000pisでの指示値(pF)、CF
はセルによって決定される定数、Wはカーボンブラック
試料の重量である。なおpF(単位:ピコファラド)
は、装置のセル内部の水銀とセル外部の電極間の静電容
量として指示される値で、この静電容量の変化から圧入
水銀量が算出される。
However, in the above formula, X 1 is the indicated value (p
F), X 2 is the indicated value (pF) at the end point of 30,000 pis, CF
Is a constant determined by the cell and W is the weight of the carbon black sample. PF (unit: picofarad)
Is a value designated as the electrostatic capacitance between the mercury inside the cell of the device and the electrode outside the cell, and the amount of press-fitted mercury is calculated from the change in this electrostatic capacitance.

これらの特性を具備するカーボンブラックは、頭部に燃
焼バーナーおよび原料油噴射ノズルを備える燃焼室とこ
れに連続する熱分解導管とから構成された発生部を2系
列設け、両発生部の熱分解導管を円筒状の主反応ゾーン
に収斂会合したY字型構造のオイルファーネス炉を用
い、別系列で発生したカーボンブラック中間生成ガス流
を主反応ゾーンに同時に高速導入して相互衝突させる方
法(特公昭62-10581号)によって製造することができ
る。
The carbon black having these characteristics is provided with two series of generating units each including a combustion chamber having a combustion burner and a raw oil injection nozzle at its head and a pyrolysis conduit continuous with the combustion chamber. A method of using a Y-shaped oil-furnace furnace with a conduit converging and converging in a cylindrical main reaction zone, simultaneously introducing high-speed carbon black intermediate product gas streams into the main reaction zone at the same time to cause mutual collision (special It can be produced according to Kosho 62-10581).

この際、凝集体空隙容積Vpの調整は、主に操業条件と
して全空気供給量、燃料油供給量、燃料燃焼率および原
料油導入量を発生部系列で変動させることにより、また
窒素吸着比表面積(NSA)およびDBP吸油量の調
整は主に炉内燃焼条件、生成カーボンブラック流の炉内
滞留時間などを制御することによって行われる、 上記のカーボンブラックは、常法に従い天然ゴム、スチ
レンブタジエンゴム、ポリブタジエンゴム、イソプレン
ゴム、ブチルゴム、その他常用カーボンブラックで補強
可能な各種合成ゴム、混合ゴムなどのエラストマーに配
合される。カーボンブラックの配合比率は、ゴム成分10
0重量部に対し35〜100重量部の割合とし、加硫剤、加硫
促進剤、老化防止剤、加硫助剤、軟化剤、可塑剤等の必
要成分とともに添加混練してタイヤトレッド用ゴム組成
物を得る。
At this time, the aggregate void volume Vp is adjusted mainly by changing the total air supply amount, the fuel oil supply amount, the fuel combustion rate, and the feedstock oil introduction amount as operating conditions in the generation part series, and also by adjusting the nitrogen adsorption specific surface area. The adjustment of (N 2 SA) and DBP oil absorption is performed mainly by controlling the combustion conditions in the furnace, the residence time in the furnace of the produced carbon black flow, and the like. It is blended with elastomers such as butadiene rubber, polybutadiene rubber, isoprene rubber, butyl rubber, various synthetic rubbers that can be reinforced with commonly used carbon black, and mixed rubbers. The compounding ratio of carbon black is 10 rubber components.
A rubber for a tire tread by mixing and kneading with necessary components such as a vulcanizing agent, a vulcanization accelerator, an antiaging agent, a vulcanization aid, a softening agent and a plasticizer in a proportion of 35 to 100 parts by weight relative to 0 parts by weight. Obtain the composition.

〔作用〕[Action]

凝集体空隙容積Vpが大きいカーボンブラックは本質的
にストラクチャーの発達したアグリゲート構造をもって
おり、ゴムに配合した際に補強性を向上させる機能があ
るが、特にこの凝集体空隙容積Vpが〔0.00976×DB
P吸油量−0.0358〕値以上の特性要件を満す場合にはカ
ーボンブラックの異方性が顕著に発達し、この作用によ
ってゴム成分の耐摩耗性を著しく向上させる。この機能
が前提特性となる窒素吸着比表面積(NSA)60〜16
0m2/gおよびDBP吸油量90〜150m/100gによる要
件と相乗的に作用して、ゴム成分に対し相対的に低位の
発熱性と高度の耐摩耗性とを同時に付与する結果を実現
する。
Carbon black having a large aggregate void volume Vp essentially has an aggregate structure with a well-developed structure, and has the function of improving the reinforcing property when compounded with rubber. In particular, this aggregate void volume Vp is [0.00976 × DB
When the P oil absorption amount-0.0358] value or more is satisfied, the anisotropy of carbon black remarkably develops, and this action remarkably improves the abrasion resistance of the rubber component. Nitrogen adsorption specific surface area (N 2 SA) 60 to 16 whose function is a prerequisite
It synergistically works with the requirement of 0 m 2 / g and DBP oil absorption of 90 to 150 m / 100 g to realize the result of simultaneously giving relatively low heat generation property and high abrasion resistance to the rubber component.

〔実施例〕〔Example〕

以下、本発明の実施例を比較例と対比して説明する。 Hereinafter, examples of the present invention will be described in comparison with comparative examples.

(1)カーボンブラックの製造 頭部にウインドボックスを介して燃焼バーナーおよび原
料油噴射ノズルを同軸的に装着した燃焼室(内径400m
m、長さ800mm、このうち円錐部分200mm)と熱分解導管
(内径60mm、長さ500mm)を備える2系列の発生部を、
内径200mm、長さ2000mmの後段広径部位と内径90mm、長
さ700mmの前段狭径部位を連設した主反応ゾーンの前面
に交角60°で収斂結合させたY字型構造のオイルファー
ネス炉を設置した。狭径部位には、交点から50mm下流に
絞り比0.65のリング部材を介設した。
(1) Manufacture of carbon black A combustion chamber (inner diameter 400m
m, length 800 mm, of which 200 mm conical part) and a pyrolysis conduit (inner diameter 60 mm, length 500 mm)
A Y-shaped oil furnace with a Y-shaped converging connection at a crossing angle of 60 ° in front of the main reaction zone in which a rear wide area with an inner diameter of 200 mm and a length of 2000 mm and a front narrow area with an inner diameter of 90 mm and a length of 700 mm are connected in series. installed. A ring member having a drawing ratio of 0.65 was interposed 50 mm downstream from the intersection at the narrow diameter portion.

原料油に比重(15/4℃)1.0703、粘度(エングラー、
40/20℃)2.10ベンゼン不溶分0.03%、挿関関係数(B
MGI)140、初期沸点103℃の芳香族炭化水素油を、ま
た燃料油としては比重(154℃)0.903、粘度(CST50
℃)16.1、残炭分5.4%、硫黄分1.8%、引火点96℃の炭
化水素油を用いた。
Specific gravity (15/4 ° C) 1.0703, viscosity (Engla,
40/20 ℃) 2.10 Benzene insoluble content 0.03%, number of relations (B
MGI) 140, aromatic hydrocarbon oil with an initial boiling point of 103 ° C, and as fuel oil, specific gravity (154 ° C) 0.903, viscosity (CST50
℃) 16.1, hydrocarbon content 5.4%, sulfur content 1.8%, flash point 96 ℃ hydrocarbon oil was used.

上記の反応炉、原料油および燃料油を用い、表Iに示し
た発生条件を適用して本発明で使用する特性範囲のカー
ボンブラック(3種類)を製造した。
Using the reaction furnace, the feedstock oil, and the fuel oil described above, the generation conditions shown in Table I were applied to produce carbon black (three types) in the characteristic range used in the present invention.

表Iの条件で製造された各カーボンブラックの窒素吸着
比表面積(NSA)、DBP吸油量、凝集体空隙容積
Vpおよび〔0.00976×DBP吸油量−0.0358〕による
関係式値を表IIに示した。
The nitrogen adsorption specific surface area (N 2 SA), DBP oil absorption amount, aggregate void volume Vp, and [0.00976 × DBP oil absorption amount-0.0358] of each carbon black produced under the conditions of Table I are shown in Table II. It was

なお、表IIのうち比較例として示したRunNo.4〜7は、
従来技術により製造された窒素吸着比表面積(N
A)60m2/g以上のハード系カーボンブラックで、いずれ
も凝集体空隙容積Vpが本発明の要件を外れるものであ
る。
In addition, Run Nos. 4 to 7 shown as comparative examples in Table II are
Nitrogen adsorption specific surface area (N 2 S
A) Hard carbon black of 60 m 2 / g or more, all of which have an aggregate void volume Vp which is outside the requirements of the present invention.

(3)ゴム配合 次に、表IIの各種カーボンブラックを表IIIに示す配合
比率で天然ゴムに配合した。
(3) Rubber compounding Next, the various carbon blacks in Table II were compounded in the natural rubber in the compounding ratios shown in Table III.

表IIIの配合物を145℃の温度で40分間加硫して得たゴム
組成物につき、各種のゴム特性を測定した。結果を表II
の配合カーボンブラックRunNo.に対応させて表IVに示し
た。
Various rubber properties were measured on the rubber composition obtained by vulcanizing the compound of Table III at a temperature of 145 ° C. for 40 minutes. The results are shown in Table II.
Corresponding to the compounding carbon black Run No.

なお、ゴム特性の測定方法および測定条件は下記によっ
た。
The rubber characteristic measuring method and measuring conditions were as follows.

(1)摩耗量 ランボーン摩耗試験機(機械式スリップ機構)を用い、
次の条件で測定した。
(1) Wear amount Using a Lambourn wear tester (mechanical slip mechanism),
The measurement was performed under the following conditions.

試験片:厚さ10mm、外径44mm エメリーホイール:GCタイプ、粒度80、硬度H 添加カーボンランダム粉:粒度80#、添加量約9g/分 エメリーホイール面と試験片の相対スリップ率:24
%、60% 試験片回転数:535rpm 試験荷重:4kg (2)tan δ Visco Elastic Spectrometer(岩本製作所製)を用い、
次の条件で測定した。
Test piece: thickness 10 mm, outer diameter 44 mm Emery wheel: GC type, grain size 80, hardness H added carbon random powder: grain size 80 #, addition amount about 9 g / min Relative slip ratio between emery wheel surface and test piece: 24
%, 60% Test piece rotation speed: 535 rpm Test load: 4 kg (2) tan δ Visco Elastic Spectrometer (manufactured by Iwamoto Seisakusho)
The measurement was performed under the following conditions.

試験片:厚さ2mm、長さ30mm、幅5mm 温度 :室温 周波数:50Hz 動的歪率:±1% (3)その他 すべてJIS K6301「一般ゴム物理試験方法」によっ
た。
Test piece: thickness 2 mm, length 30 mm, width 5 mm Temperature: room temperature Frequency: 50 Hz Dynamic strain rate: ± 1% (3) Others All were based on JIS K6301 "General rubber physical test method".

表IVの結果から、本発明のカーボンブラック特性要件を
満たすカーボンブラックを配合した実施例によるゴム組
成物は、凝集体空隙容積が本発明の関係式値を満たさな
いカーボンブラックを配合した比較例によるゴム組成物
に比べ、同等の窒素吸着比表面積水準において同程度の
損失係数(tanδ)を維持しながら耐摩耗性は有意に向
上していることが認められる。
From the results of Table IV, the rubber composition according to the example in which the carbon black satisfying the carbon black characteristic requirements of the present invention was blended, the aggregate void volume was in accordance with the comparative example in which the carbon black not satisfying the relational expression value of the present invention was blended. It is recognized that the wear resistance is significantly improved while maintaining the same loss factor (tan δ) at the same nitrogen adsorption specific surface area level as compared with the rubber composition.

〔発明の効果〕 以上のとおり、本発明に係るカーボンブラックは高度に
ストラクチャーが発達した異方性の大きなアグリゲート
構造を有しており、配合ゴムに対して高度の耐摩耗性と
相対的に低位の発熱性を同時に付与することができるも
のである。したがって、苛酷な走行環境下で使用される
トラック、バスなどの大型タイヤ用トレッドゴムに配合
して、その要求性能を十分に満足しうる有用性がもたら
される。
[Effects of the Invention] As described above, the carbon black according to the present invention has a highly anisotropic aggregate structure with a highly developed structure, and has a relatively high abrasion resistance relative to the compounded rubber. A low exothermicity can be imparted at the same time. Therefore, it can be compounded with a tread rubber for a large tire such as a truck or a bus used in a harsh traveling environment to bring about a usefulness that can sufficiently satisfy the required performance.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】窒素吸着比表面積(NSA)が60〜1
60m2/g、DBP吸油量が90〜150m/100gのバード
系領域に属し、かつ凝集体空隙容積Vp(m/g)が
〔0.00976×DBP吸油量−0.0358〕式により算出され
る値以上の選択的特性を有するタイヤトレッドゴム用カ
ーボンブラック。
1. A nitrogen adsorption specific surface area (N 2 SA) of 60 to 1
60 m 2 / g, DBP oil absorption amount belongs to a bird system region of 90 to 150 m / 100 g, and the aggregate void volume Vp (m / g) is not less than the value calculated by the formula [0.00976 × DBP oil absorption amount-0.0358]. Carbon black for tire tread rubber having selective properties.
JP63182378A 1988-07-11 1988-07-21 Carbon black for tire tread rubber Expired - Fee Related JPH0637582B2 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
JP63182378A JPH0637582B2 (en) 1988-07-21 1988-07-21 Carbon black for tire tread rubber
KR1019890009848A KR930002554B1 (en) 1988-07-11 1989-07-11 Carbon black for tire tread rubber
FR8909601A FR2634491B1 (en) 1988-07-21 1989-07-18 CARBON BLACK FOR TIRE TRUCK RUBBER
US07/759,378 US5198205A (en) 1988-07-21 1991-09-13 Carbon black for tire tread rubber

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP63182378A JPH0637582B2 (en) 1988-07-21 1988-07-21 Carbon black for tire tread rubber

Publications (2)

Publication Number Publication Date
JPH0232136A JPH0232136A (en) 1990-02-01
JPH0637582B2 true JPH0637582B2 (en) 1994-05-18

Family

ID=16117265

Family Applications (1)

Application Number Title Priority Date Filing Date
JP63182378A Expired - Fee Related JPH0637582B2 (en) 1988-07-11 1988-07-21 Carbon black for tire tread rubber

Country Status (3)

Country Link
JP (1) JPH0637582B2 (en)
KR (1) KR930002554B1 (en)
FR (1) FR2634491B1 (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2649716B1 (en) * 1989-07-13 1991-12-06 Tokai Carbon Kk CARBON BLACK FOR TIRE TREAD RUBBER
JPH0649802B2 (en) * 1989-07-18 1994-06-29 東海カーボン株式会社 Rubber composition
JP2002327134A (en) * 2001-05-07 2002-11-15 Tokai Carbon Co Ltd Carbon black for tire tread rubber
JP4607564B2 (en) * 2004-12-07 2011-01-05 株式会社ブリヂストン Rubber composition and pneumatic tire using the same
JP2008163212A (en) * 2006-12-28 2008-07-17 Bridgestone Corp Rubber composition and pneumatic tire using the same

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5274647A (en) * 1975-12-17 1977-06-22 Tokai Carbon Kk Rubber compositions
JPS6123107A (en) * 1984-07-12 1986-01-31 Seiko Epson Corp Contact lens
JPS61133245A (en) * 1984-11-30 1986-06-20 Yokohama Rubber Co Ltd:The Rubber composition for tire tread
JPS6230137A (en) * 1985-07-31 1987-02-09 Yokohama Rubber Co Ltd:The Rubber composition for tire
JPS6296542A (en) * 1985-10-23 1987-05-06 Yokohama Rubber Co Ltd:The Rubber composition for high-speed large pneumatic tire
JPS6397646A (en) * 1986-10-14 1988-04-28 Yokohama Rubber Co Ltd:The Rubber composition for tire tread

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59140241A (en) * 1983-01-31 1984-08-11 Tokai Carbon Co Ltd Rubber composition

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5274647A (en) * 1975-12-17 1977-06-22 Tokai Carbon Kk Rubber compositions
JPS6123107A (en) * 1984-07-12 1986-01-31 Seiko Epson Corp Contact lens
JPS61133245A (en) * 1984-11-30 1986-06-20 Yokohama Rubber Co Ltd:The Rubber composition for tire tread
JPS6230137A (en) * 1985-07-31 1987-02-09 Yokohama Rubber Co Ltd:The Rubber composition for tire
JPS6296542A (en) * 1985-10-23 1987-05-06 Yokohama Rubber Co Ltd:The Rubber composition for high-speed large pneumatic tire
JPS6397646A (en) * 1986-10-14 1988-04-28 Yokohama Rubber Co Ltd:The Rubber composition for tire tread

Also Published As

Publication number Publication date
JPH0232136A (en) 1990-02-01
FR2634491B1 (en) 1994-04-01
KR900001797A (en) 1990-02-27
FR2634491A1 (en) 1990-01-26
KR930002554B1 (en) 1993-04-03

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