JP2862563B2 - Cap-based tires - Google Patents

Cap-based tires

Info

Publication number
JP2862563B2
JP2862563B2 JP1142484A JP14248489A JP2862563B2 JP 2862563 B2 JP2862563 B2 JP 2862563B2 JP 1142484 A JP1142484 A JP 1142484A JP 14248489 A JP14248489 A JP 14248489A JP 2862563 B2 JP2862563 B2 JP 2862563B2
Authority
JP
Japan
Prior art keywords
parts
rubber
weight
tire
silica
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
JP1142484A
Other languages
Japanese (ja)
Other versions
JPH037602A (en
Inventor
彰 岡村
一彦 末吉
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.)
Toyo Tire Corp
Original Assignee
Toyo Tire and Rubber 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 Toyo Tire and Rubber Co Ltd filed Critical Toyo Tire and Rubber Co Ltd
Priority to JP1142484A priority Critical patent/JP2862563B2/en
Publication of JPH037602A publication Critical patent/JPH037602A/en
Application granted granted Critical
Publication of JP2862563B2 publication Critical patent/JP2862563B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02TCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO TRANSPORTATION
    • Y02T10/00Road transport of goods or passengers
    • Y02T10/80Technologies aiming to reduce greenhouse gasses emissions common to all road transportation technologies
    • Y02T10/86Optimisation of rolling resistance, e.g. weight reduction 

Landscapes

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

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は高速耐久性、耐摩耗性、耐偏摩耗性、低転動
抵抗性等に優れ、更には耐末期のカツト、チツプ性にも
優れたキヤツプベース構造のタイヤに関する。
DETAILED DESCRIPTION OF THE INVENTION (Industrial application field) The present invention is excellent in high-speed durability, abrasion resistance, uneven wear resistance, low rolling resistance, and the like, and is also excellent in end-use cutting and chipping properties. The present invention relates to a tire having an excellent cap-based structure.

(従来の技術) 従来、耐摩耗性、耐偏摩耗性を向上させると耐発熱性
が悪化する為、キヤツプベース構造のタイヤを採用しベ
ースに低発熱性ゴムを用いている。更に耐久性、耐摩耗
性を向上させるには低発熱性のベースゴムを開発する必
要がある。そのためには充填剤(フイラー)としてカー
ボンブラツクの単独使用では限度があつた。そこでフイ
ラーとしてシリカとカーボンブラツクの併用について検
討を行い、ベーストレツドにおいて両者の特定比率の使
用及びシランカツプリング剤、特定の結合剤の使用によ
り、ベーストレツドとしての性能を満足し低発熱、高破
壊引裂強度、耐末期のカツト、チツプ性が改善されるこ
とを見い出した。
(Prior Art) Conventionally, heat resistance deteriorates when wear resistance and uneven wear resistance are improved. Therefore, a tire having a cap-based structure is employed and a low heat-generating rubber is used as a base. In order to further improve durability and abrasion resistance, it is necessary to develop a base rubber having low heat generation. Therefore, there was a limit in using carbon black alone as a filler (filler). Therefore, we examined the combination of silica and carbon black as a filler, and by using a specific ratio of both and using a silane coupling agent and a specific binder in the base led, the performance as a base led was satisfied and low heat generation and high fracture tear strength were achieved. It was found that the cutting and chipping properties at the end of life were improved.

(発明が解決しようとする課題) 本発明の目的は高速耐久性、耐摩耗性、耐偏摩耗性、
低転動抵抗性等に優れ、更には耐末期のカツト、チツプ
性にも優れたキヤツプベース構造のタイヤを提供するこ
とにある。
(Problems to be Solved by the Invention) The object of the present invention is to provide high-speed durability, wear resistance, uneven wear resistance,
An object of the present invention is to provide a tire having a cap-based structure which is excellent in low rolling resistance and the like, and which is also excellent in end-time cutting and chipping properties.

(課題を解決するための手段) 本発明はトレツドゴムがトレツド表面部のキヤツプゴ
ムと、ベルトに接する部分のベースゴムの2層構造より
なるタイヤにおいて、ゴム成分100重量部に対してカー
ボンブラツクを10〜40重量部、シリカを10〜40重量部、
両者のトータルフイラー量20〜80重量部を含有し、トー
タルフイラー中のシリカ量は25〜75%であり、更にシリ
カ量の5〜20%のシランカツプリング剤を含有し、更に
レゾルシンもしくはレゾルシン誘導体、ならびにメラミ
ン1分子当たり、結合ホルマリン数およびメトキシ基数
が、 4≦(結合ホルマリン数)≦6、 2≦(メトキシ基数)<6の範囲で、かつ一量体含量
が60〜90%のメラミン誘導体を含有するゴム組成物より
得られるベーストレツドを使用したことを特徴とするキ
ヤツプベース構造のタイヤに係る。
(Means for Solving the Problems) The present invention relates to a tire having a two-layer structure in which a tread rubber has a cap rubber on a tread surface portion and a base rubber in a portion in contact with a belt. 40 parts by weight, 10 to 40 parts by weight of silica,
The total filler content of both contains 20 to 80 parts by weight, the silica content in the total filler is 25 to 75%, and further contains a silane coupling agent in an amount of 5 to 20% of the silica content, and further contains resorcinol or a resorcinol derivative. And the number of bound formalin and the number of methoxy groups per molecule of melamine are in the range of 4 ≦ (number of bound formalin) ≦ 6 and 2 ≦ (number of methoxy groups) <6, and the monomer content is 60 to 90%. The present invention relates to a tire having a cap-based structure using a base tread obtained from a rubber composition containing

本発明のタイヤのベーストレツドのゴム成分としては
天然ゴム(NR)、ブタンジエンゴム(BR)、スチレンブ
タジエンゴム(SBR)、イソプレンゴム(IR)及びこれ
らのブレンドを使用することができる。
As the rubber component of the base tread of the tire of the present invention, natural rubber (NR), butanediene rubber (BR), styrene butadiene rubber (SBR), isoprene rubber (IR) and blends thereof can be used.

本発明はゴム成分100重量部に対してカーボンブラツ
クを10〜40重量部、シリカを10〜40重量部、両者のトー
タルフイラー量20〜80重量部を含有し、トータルフイラ
ー中のシリカ量は25〜75%であり、更にシリカ量の5〜
20%のシランカツプリング剤を含有するゴム組成物より
得られるベーストレツドを使用したことを特徴とする。
The present invention contains 10 to 40 parts by weight of carbon black, 10 to 40 parts by weight of silica, and 20 to 80 parts by weight of the total filler of both, based on 100 parts by weight of the rubber component, and the amount of silica in the total filler is 25. ~ 75%, and 5 ~ 5
It is characterized by using a base led obtained from a rubber composition containing 20% of a silane coupling agent.

カーボンブラツク又はシリカが10重量部未満及び両者
のトータルフイラー量が20重量部未満では転動抵抗性は
優れるが、偏摩耗性、摩耗性、末期のカツト性が著しく
低下する。カーボンブラツク又はシリカが40重量部を越
え或いは両者のトータルフイラー量が80重量部を越える
場合は転動抵抗性が悪化し、補強剤を増量した割には末
期の摩耗性が改良されず、ベルト耐久性の低下がみられ
る。更にトータルフイラー中のシリカ量が25%未満では
転動抵抗性、ベルト耐久性の改良がみられず、又75%を
越えると末期のカツト性、摩耗性の改良がみられない。
If the carbon black or silica is less than 10 parts by weight and the total filler content of both is less than 20 parts by weight, the rolling resistance is excellent, but the uneven wear, abrasion, and end-stage cutting properties are significantly reduced. If the carbon black or silica exceeds 40 parts by weight or the total filler content of both exceeds 80 parts by weight, the rolling resistance deteriorates, and the wear at the final stage is not improved even if the reinforcing agent is increased, and the belt is not improved. There is a decrease in durability. If the amount of silica in the total filler is less than 25%, the rolling resistance and belt durability are not improved, and if it exceeds 75%, the cutting properties and abrasion at the end are not improved.

本発明で用いられるシランカツプリング剤としては各
種公知のものを使用でき、代表例としてγ−メルカプト
プロピルトリメトキシシラン(ユニオンカーバイド、A1
89)、γ−アミノプロピルトリエトキシシラン(ユニオ
ンカーバイド、A1100)、ビス〔3−(トリエトキシシ
リル)プロピル〕テトラスルフアイド(デグサ、Si-69
等)を挙げることができる。シランカツプリング剤の量
がシリカ量の5%未満の場合は補強性(硬度、モジユラ
スの低下、引張強さ)が劣り発熱性が悪化する。20%を
越える場合は性能的に顕著な差はみられないがコストが
向上する。
Various known silane coupling agents can be used as the silane coupling agent in the present invention. Typical examples thereof include γ-mercaptopropyltrimethoxysilane (union carbide, A1
89), γ-aminopropyltriethoxysilane (Union Carbide, A1100), bis [3- (triethoxysilyl) propyl] tetrasulfide (Degussa, Si-69
Etc.). When the amount of the silane coupling agent is less than 5% of the amount of silica, the reinforcing properties (hardness, lowering of modulus, tensile strength) are inferior, and the heat generation becomes worse. If it exceeds 20%, there is no significant difference in performance, but the cost is improved.

本発明では使用末期のカツト、チツプ性を改良するた
めに、上記ベーストレツド用ゴム組成物中に、更にレゾ
ルシンもしくはレゾルシン誘導体、ならびにメラミン1
分子当たり、結合ホルマリン数およびメトキシ基数が、 4≦(結合ホルマリン数)≦6、 2≦(メトキシ基数)<6の範囲で、かつ一量体含量
が60〜90%のメラミン誘導体を配合することが有効であ
る。
In the present invention, resorcinol or a resorcinol derivative, and melamine 1
A melamine derivative having a number of bound formalin and a number of methoxy groups per molecule of 4 ≦ (number of bound formalin) ≦ 6, 2 ≦ (number of methoxy groups) <6, and a monomer content of 60 to 90%. Is valid.

ここでレゾルシン誘導体としては、レゾルシン・ホル
ムアルデヒド樹脂、レゾルシン・ホルムアルデヒド樹脂
とアルキルフエノール・ホルムアルデヒド樹脂との溶融
混合物などが挙げられる。又、メラミン誘導体としては
メラミン1分子当たり、結合ホルマリン数およびメトキ
シ基数が、 4≦(結合ホルマリン数)≦6、 4≦(メトキシ基数)<6であることが好ましい。
Here, examples of the resorcinol derivative include a resorcinol / formaldehyde resin and a molten mixture of a resorcinol / formaldehyde resin and an alkylphenol / formaldehyde resin. Further, as the melamine derivative, the number of bound formalin and the number of methoxy groups per one molecule of melamine are preferably 4 ≦ (number of bound formalin) ≦ 6 and 4 ≦ (number of methoxy groups) <6.

本発明のメラミン誘導体において、一量体含量は多い
ほど加硫ゴムは優れた動的特性を示し、なおかつ未加硫
ゴム配合物は高いスコーチ安定性を示す。即ち一量体含
量が60%未満では、たとえメラミン1分子当たりの結合
ホルマリン数及びメトキシ基数が、本発明の範囲にあつ
たとしても、優れた動的特性、更には高いスコーチ安定
性は得られない。一量体含量が90%を越えると、通常の
製造方法では得られず、特別の精製工程を必要とするた
め、製造コストが大巾に増加し、工業的価値が低下する
ため、実用上一量体含量は60〜90%の範囲が選択され
る。
In the melamine derivative of the present invention, the higher the monomer content, the more excellent the vulcanized rubber exhibits dynamic properties, and the more the unvulcanized rubber compound exhibits high scorch stability. That is, when the monomer content is less than 60%, excellent dynamic characteristics and high scorch stability can be obtained even if the number of bound formalin and methoxy group per melamine molecule falls within the range of the present invention. Absent. When the monomer content exceeds 90%, it cannot be obtained by a normal production method, and a special purification step is required. Therefore, the production cost is greatly increased, and the industrial value is reduced. The content of the monomer is selected in the range of 60 to 90%.

またメラミン1分子当たりの結合ホルマリン数は多い
程、加硫ゴムの動的特性が優れる傾向にあり、結合ホル
マリン数が4未満では充分な効果が得られない。
In addition, as the number of bound formalin per molecule of melamine is larger, the dynamic properties of the vulcanized rubber tend to be more excellent.

またメラミン誘導体中のメトキシ基とフリーのメチロ
ール基の比率も、加硫ゴムの動的特性ならびに未加硫ゴ
ムの加工性に大巾に影響を与える。即ち、メラミン誘導
体の一量体含量ならびにメラミン1分子当たりの結合ホ
ルマリン数が一定としても、メトキシ基が少ない程、フ
リーのメチロール基数が多い事を意味し、加硫ゴムの動
的特性は若干向上する傾向にあるものの、未加硫ゴムの
加工性は大巾に低下する点が存在し、その傾向はシリカ
を含有する系で顕著である。
The ratio of methoxy groups to free methylol groups in the melamine derivative also has a significant effect on the dynamic properties of the vulcanized rubber and the processability of the unvulcanized rubber. In other words, even if the monomer content of the melamine derivative and the number of bound formalins per melamine molecule are constant, the smaller the number of methoxy groups, the greater the number of free methylol groups, and the dynamic properties of the vulcanized rubber are slightly improved. However, there is a point where the processability of the unvulcanized rubber is greatly reduced, and this tendency is remarkable in a system containing silica.

本発明においてレゾルシンもしくはレゾルシン誘導体
は、ゴム100重量部に対し、通常0.1〜7重量部、好まし
くは0.3〜5重量部配合される。又、メラミン誘導体
は、ゴム100重量部に対し、通常0.5〜7重量部、好まし
くは1〜5重量部配合される。
In the present invention, resorcinol or a resorcinol derivative is generally added in an amount of 0.1 to 7 parts by weight, preferably 0.3 to 5 parts by weight, based on 100 parts by weight of rubber. The melamine derivative is usually added in an amount of 0.5 to 7 parts by weight, preferably 1 to 5 parts by weight, based on 100 parts by weight of the rubber.

本発明のタイヤは上記成分を通常の加工装置、例えば
ロール、バンバリーミキサー、ニーダーなどにより混練
することにより得られるゴム組成物をベーストレツド部
に使用して常法により製造できる。また上記成分の他に
公知の加硫剤、加硫促進剤、加硫促進助剤、加硫遅延
剤、有機過酸化物、補強剤、可塑剤、老化防止剤、粘着
付与剤、着色剤等を添加できることは勿論である。
The tire of the present invention can be produced by a conventional method using a rubber composition obtained by kneading the above components with a usual processing device, for example, a roll, a Banbury mixer, a kneader, or the like, for a base tread portion. In addition to the above components, known vulcanizing agents, vulcanization accelerators, vulcanization accelerating aids, vulcanization retardants, organic peroxides, reinforcing agents, plasticizers, antioxidants, tackifiers, coloring agents, etc. Can of course be added.

上記ゴム組成物をベーストレツドゴムとして用いる以
外、タイヤの製造は公知の方法に従つて行うことができ
る。ベースゴムの厚みはノンスキツドベース(ベルト部
からトレツド溝底までの距離)の30%以上、好ましくは
50%以上が望ましい。キヤツプゴム組成物としては例え
ば天然ゴム(NR)、ブタジエンゴム(BR)、スチレンブ
タジエンゴム(SBR)、イソプレンゴム(IR)及びこれ
らのブレンドを使用することができるが、ゴム成分中に
おけるスチレン量は20重量%以下とするのが好ましい。
キヤツプゴムの厚みはノンキスツドベース(ベルト部か
らトレツド溝底までの距離)の70%以下、好ましくは50
%以下が望ましい。
Except for using the rubber composition as a base-tread rubber, the tire can be manufactured according to a known method. The thickness of the base rubber is 30% or more of the non-skid base (the distance from the belt to the bottom of the tread groove), preferably
50% or more is desirable. As the cap rubber composition, for example, natural rubber (NR), butadiene rubber (BR), styrene butadiene rubber (SBR), isoprene rubber (IR) and a blend thereof can be used. % By weight or less.
The thickness of the cap rubber is 70% or less of the non-kissed base (the distance from the belt to the bottom of the tread groove), preferably 50%.
% Is desirable.

(発明の効果) 本発明のタイヤは高速耐久性、耐摩耗性、耐偏摩耗
性、低転動抵抗性等に優れ、更には耐末期のカツト、チ
ツプ性にも優れている。
(Effect of the Invention) The tire of the present invention is excellent in high-speed durability, wear resistance, uneven wear resistance, low rolling resistance, and the like, and is also excellent in end-stage cut and chip resistance.

(実施例) 以下に実施例及び比較例を挙げて説明する。尚、配合
は重量部である。
(Example) Hereinafter, an example and a comparative example will be described. In addition, the composition is part by weight.

実施例及び比較例 NR(RSS♯1)100部、HAFカーボンブラツク各部、ISA
Fカーボンブラツク部、シリカ各部、Si-69各部、レゾル
シン各部、スミカノール620及び507各部、ヘキサミン各
部、亜鉛華4部、ステアリン酸2部、老化防止剤(6PP
D)1部、加硫促進剤(CZ)1部(配合No.Fのみ1.2
部)、硫黄1.5部を、バンバリーミキサーにより充分に
混練しベーストレツド用ゴム組成物を得た。ここでスミ
カノール620は住友化学製のレゾルシン・アルキルフエ
ノール・ホルマリンの共縮合物、スミカノール507は同
様住友化学製のメラミン・アルムアルデヒド・メタノー
ルの重縮合物50重量%、シリカ35重量%、プロセスオイ
ル15重量%の混合物である。
Examples and Comparative Examples 100 parts of NR (RSS♯1), parts of HAF carbon black, ISA
F Carbon black part, silica parts, Si-69 parts, resorcinol parts, Sumicanol 620 and 507 parts, hexamine parts, zinc white 4 parts, stearic acid 2 parts, antioxidant (6PP
D) 1 part, vulcanization accelerator (CZ) 1 part (Formulation No. F only 1.2
Parts) and 1.5 parts of sulfur were sufficiently kneaded with a Banbury mixer to obtain a base-tread rubber composition. Here, Sumikanol 620 is a co-condensate of resorcin, alkylphenol and formalin manufactured by Sumitomo Chemical, and Sumicanol 507 is a 50% by weight polycondensate of melamine / alumaldehyde / methanol manufactured by Sumitomo Chemical, 35% by weight of silica, and process oil 15 % By weight of the mixture.

得られたゴム組成物を145℃で30分間、モールド加硫
し、その特性を測定した。結果を第1表に示す。Hsは硬
さ、M300は300%引張応力、TBは引張強さを示す、 グツドリツチ発熱テストは測定温度50℃、ストローク
5mm、回転数1650rpmで平衡になつた表面温度を測定し
た。
The obtained rubber composition was subjected to mold vulcanization at 145 ° C. for 30 minutes, and its properties were measured. The results are shown in Table 1. Hs indicates hardness, M 300 indicates 300% tensile stress, T B indicates tensile strength.
The surface temperature at which equilibrium was reached at 5 mm and a rotation speed of 1650 rpm was measured.

屈曲試験はJIS K6301に従い、比較例1を100として指
数表示した。数値の大きい程良好である。
The bending test was performed according to JIS K6301, and the index was indicated as an index with Comparative Example 1 being 100. The higher the value, the better.

試験例 第2表に示すキヤツプベース構造のタイヤのベルト耐
久性、転動抵抗性、タイヤライフ及び使用末期状態を10
00R20 14PRのタイヤを製作して下記の方法により測定し
た。
Test Example The belt durability, rolling resistance, tire life and end-of-use state of the tire having the cap-based structure shown in Table 2
00R20 14PR tire was manufactured and measured by the following method.

(a)ベルト耐久性 ドラム(台上耐久)テストにて故障する迄、タイヤを
走行させ、その走行距離をタイヤIを100として指数表
示した。数値の大きい方が耐久性は良好である。
(A) Belt durability The tire was run until a failure occurred in a drum (table durability) test, and the running distance was indicated as an index with the tire I as 100. The larger the value, the better the durability.

(b)転動抵抗性 米国自動車技術協会報文(SAE)第770875号に記載の
測定法に準じ、タイヤが高温状態になつた時点での転動
抵抗を測定し、タイヤIを100として指数表示した。数
値の小さい方が良好である。
(B) Rolling Resistance The rolling resistance at the time when the tires reached a high temperature state was measured according to the measurement method described in the American Automobile Technology Association Bulletin (SAE) No. 770875, and the tire I was indexed as 100. displayed. The smaller the value, the better.

(c)タイヤライフ 実車テスト評価にて取り外しされる迄の距離をタイヤ
Iを100として指数表示した。数値の大きい方が耐久性
が良好である。
(C) Tire life The distance until the tire was removed in the actual vehicle test evaluation was indicated as an index with the tire I as 100. The larger the value, the better the durability.

(d)使用末期状態 上記(c)で取り外しされたタイヤのトレツドを取り
除きスチールベルトに達しているキズの大きさを測定し
タイヤIを100として指数表示した。数値の大きい方が
耐末期状態が良好である。
(D) End-of-use state The tread of the tire removed in (c) above was removed, and the size of the scratch reaching the steel belt was measured. The larger the value, the better the end-life state.

───────────────────────────────────────────────────── フロントページの続き (56)参考文献 特開 昭47−40704(JP,A) 特開 昭59−53206(JP,A) 特開 平1−92247(JP,A) 特開 昭61−287802(JP,A) 特開 昭63−180505(JP,A) 特開 昭48−72241(JP,A) 特公 昭56−52057(JP,B2) 特公 昭54−39426(JP,B2) (58)調査した分野(Int.Cl.6,DB名) B60C 1/00 B60C 11/00 C08L 1/00 - 101/14──────────────────────────────────────────────────続 き Continuation of front page (56) References JP-A-47-40704 (JP, A) JP-A-59-53206 (JP, A) JP-A-1-92247 (JP, A) JP-A 61- 287802 (JP, A) JP-A-63-180505 (JP, A) JP-A-48-72241 (JP, A) JP-B-56-52057 (JP, B2) JP-B-54-39426 (JP, B2) (58) Field surveyed (Int.Cl. 6 , DB name) B60C 1/00 B60C 11/00 C08L 1/00-101/14

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】トレツドゴムがトレツド表面部のキヤツプ
ゴムと、ベルトに接する部分のベースゴムの2層構造よ
りなるタイヤにおいて、ゴム成分100重量部に対してカ
ーボンブラツクを10〜40重量部、シリカを10〜40重量
部、両者のトータルフイラー量20〜80重量部を含有し、
トータルフイラー中のシリカ量は25〜75%であり、更に
シリカ量の5〜20%のシランカツプリング剤を含有し、
更にレゾルシンもしくはレゾルシン誘導体、ならびにメ
ラミン1分子当たり、結合ホルマリン数およびメトキシ
基数が、 4≦(結合ホルマリン数)≦6、 2≦(メトキシ基数)<6の範囲で、かつ一量体含量が
60〜90%のメラミン誘導体を含有するゴム組成物より得
られるベーストレツドを使用したことを特徴とするキヤ
ツプベース構造のタイヤ。
In a tire having a two-layer structure in which a tread rubber has a cap rubber on a tread surface portion and a base rubber in a portion in contact with a belt, 10 to 40 parts by weight of carbon black and 10 to 40 parts by weight of silica are added to 100 parts by weight of a rubber component. ~ 40 parts by weight, containing both 20-80 parts by weight of total filler,
The amount of silica in the total filler is 25 to 75%, and further contains a silane coupling agent of 5 to 20% of the amount of silica,
Furthermore, the number of bound formalin and the number of methoxy groups per molecule of resorcinol or resorcinol derivative and melamine are in the range of 4 ≦ (number of bound formalin) ≦ 6, 2 ≦ (number of methoxy groups) <6, and the monomer content is
A tire having a cap-based structure using a base tread obtained from a rubber composition containing 60 to 90% of a melamine derivative.
JP1142484A 1989-06-05 1989-06-05 Cap-based tires Expired - Fee Related JP2862563B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1142484A JP2862563B2 (en) 1989-06-05 1989-06-05 Cap-based tires

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1142484A JP2862563B2 (en) 1989-06-05 1989-06-05 Cap-based tires

Publications (2)

Publication Number Publication Date
JPH037602A JPH037602A (en) 1991-01-14
JP2862563B2 true JP2862563B2 (en) 1999-03-03

Family

ID=15316397

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1142484A Expired - Fee Related JP2862563B2 (en) 1989-06-05 1989-06-05 Cap-based tires

Country Status (1)

Country Link
JP (1) JP2862563B2 (en)

Families Citing this family (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH05271477A (en) * 1992-03-30 1993-10-19 Toyo Tire & Rubber Co Ltd Tread rubber composition
EP0609499A1 (en) * 1992-11-06 1994-08-10 Hydril Company Carbon black pair with different particle size and improved rubber stock
CA2138726A1 (en) * 1994-09-13 1996-03-14 Bharat Kanchanlal Kansupada Tire with coated silica reinforced rubber tread
US6044882A (en) * 1995-03-07 2000-04-04 The Goodyear Tire & Rubber Company Tire having silica reinforced rubber tread with outer cap containing carbon black
CA2171392A1 (en) * 1995-04-21 1996-10-22 Jean-Claude Joseph Marie Kihn Tire with cap/base construction tread
US5718781A (en) * 1995-06-07 1998-02-17 The Goodyear Tire & Rubber Company Tire having silica reinforced rubber tread containing carbon fibers
CA2173917A1 (en) * 1995-07-20 1997-01-21 Manuela Pompei Silica reinforced treaded tire with conductive shoulder and crown portions
US5733393A (en) * 1996-01-17 1998-03-31 The Goodyear Tire & Rubber Company Tire having good diverse properties
US5718782A (en) * 1996-03-07 1998-02-17 The Goodyear Tire & Rubber Company Truck tire with cap/base construction tread
US6095217A (en) * 1996-07-11 2000-08-01 Bridgestone Corporation Pneumatic tire including cap layer and base layer
US6036800A (en) * 1996-08-28 2000-03-14 The Goodyear Tire & Rubber Company Method of preparing tire with tread of cap/base construction
US6336486B1 (en) * 1997-04-04 2002-01-08 Bridgestone Corporation Pneumatic radical tire having cap base tread
DE19834804A1 (en) * 1998-08-01 2000-02-03 Continental Ag Rubber compound
KR100507770B1 (en) * 1998-09-03 2005-11-21 한국타이어 주식회사 Low Fuel Economy Tire Tread Rubber Composition
US6289958B1 (en) * 1998-10-19 2001-09-18 The Goodyear Tire & Rubber Company Tire with tread containing electrically conductive stitched thread
US6220319B1 (en) * 1998-10-19 2001-04-24 The Goodyear Tire & Rubber Company Tire with tread containing electrically conductive staples
KR100384643B1 (en) * 2000-06-22 2003-05-22 한국타이어 주식회사 Rubber composition for tire tread
US6581660B2 (en) * 2001-03-15 2003-06-24 The Goodyear Tire & Rubber Company Tire with rubber tread of cap/base construction wherein the tread base rubber composition contains combination of anti-reversion agents
US6868878B2 (en) * 2002-10-14 2005-03-22 Michelin Recherche Et Technique S.A. Pneumatic tire including belt cushion section and having conductive path between belt layer and carcass and method of making same
US7028734B2 (en) * 2003-06-24 2006-04-18 The Goodyear Tire & Rubber Company Truck tire with cap/base construction tread
JP2007161900A (en) * 2005-12-14 2007-06-28 Sumitomo Rubber Ind Ltd Rubber composition for tread of motocross tire for two-wheeled vehicle
US7735533B2 (en) * 2005-12-20 2010-06-15 The Goodyear Tire & Rubber Company Heavy duty tire with silica-rich polyisoprene rubber based intermediate transition layer
US7740034B2 (en) * 2005-12-20 2010-06-22 The Goodyear Tire & Rubber Company Light duty tire with silica-rich polyisoprene rubber based intermediate transition layer
BRPI0805232A2 (en) * 2007-11-27 2009-09-15 Goodyear Tire & Rubber silica tread tire having self-condensing resin
US8439095B2 (en) * 2010-03-16 2013-05-14 The Goodyear Tire & Rubber Company Tire having tread with an internal softer transition rubber layer containing short fiber reinforcement
JP5768901B2 (en) * 2012-05-31 2015-08-26 横浜ゴム株式会社 Pneumatic tire

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