JPH0348025B2 - - Google Patents
Info
- Publication number
- JPH0348025B2 JPH0348025B2 JP61030680A JP3068086A JPH0348025B2 JP H0348025 B2 JPH0348025 B2 JP H0348025B2 JP 61030680 A JP61030680 A JP 61030680A JP 3068086 A JP3068086 A JP 3068086A JP H0348025 B2 JPH0348025 B2 JP H0348025B2
- Authority
- JP
- Japan
- Prior art keywords
- rubber
- splice
- cut
- strip
- vulcanization
- 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 - Lifetime
Links
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 36
- 229920001971 elastomer Polymers 0.000 claims description 27
- 239000005060 rubber Substances 0.000 claims description 27
- 239000000203 mixture Substances 0.000 claims description 12
- 229920000642 polymer Polymers 0.000 claims description 6
- 238000004073 vulcanization Methods 0.000 description 12
- 239000004568 cement Substances 0.000 description 11
- 238000000034 method Methods 0.000 description 10
- 239000000853 adhesive Substances 0.000 description 8
- 230000001070 adhesive effect Effects 0.000 description 8
- 230000007423 decrease Effects 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 4
- 238000010030 laminating Methods 0.000 description 4
- 244000043261 Hevea brasiliensis Species 0.000 description 3
- 229920003049 isoprene rubber Polymers 0.000 description 3
- 238000000465 moulding Methods 0.000 description 3
- 229920003052 natural elastomer Polymers 0.000 description 3
- 229920001194 natural rubber Polymers 0.000 description 3
- 239000005062 Polybutadiene Substances 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 238000003475 lamination Methods 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 229920002857 polybutadiene Polymers 0.000 description 2
- ZZMVLMVFYMGSMY-UHFFFAOYSA-N 4-n-(4-methylpentan-2-yl)-1-n-phenylbenzene-1,4-diamine Chemical compound C1=CC(NC(C)CC(C)C)=CC=C1NC1=CC=CC=C1 ZZMVLMVFYMGSMY-UHFFFAOYSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 1
- 230000003712 anti-aging effect Effects 0.000 description 1
- 239000010692 aromatic oil Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- DEQZTKGFXNUBJL-UHFFFAOYSA-N n-(1,3-benzothiazol-2-ylsulfanyl)cyclohexanamine Chemical compound C1CCCCC1NSC1=NC2=CC=CC=C2S1 DEQZTKGFXNUBJL-UHFFFAOYSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 238000010058 rubber compounding Methods 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 238000009864 tensile test Methods 0.000 description 1
- KAKZBPTYRLMSJV-UHFFFAOYSA-N vinyl-ethylene Natural products C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 1
- 235000014692 zinc oxide Nutrition 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Landscapes
- Lining Or Joining Of Plastics Or The Like (AREA)
- Tyre Moulding (AREA)
Description
〔発明の技術分野〕
本発明は、タイヤトレツドのスプラシス面(接
合面)の接着性を向上せしめたタイヤ成形方法に
関する。
〔従来の技術〕
従来、ゴム組成物からなる帯状物の一端と他端
とを接合して環状のタイヤトレツドとする際のタ
イヤトレツドスプライスの方法としては、大別し
て2種類の方法がある。すなわち、天然ゴム
(NR)又はイソプレンゴム(IR)を主体とする
トレツドで行われるもので、押出成型機から押出
された帯状物をカツターで横断的にバイアスに切
断してスプライス面を形成させ、スプライス面同
士をそのまま貼合する方法、およびスチレン−
ブタジエン共重合体ゴム(SBR)又はブタジエ
ンゴム(BR)を主体とするトレツドで行われる
もので、押出後の帯状物をカツターで横断的にバ
イアスに切断して形成したスプライス面に粘着性
に優れたゴムセメントを塗布し、これを乾燥させ
た後、貼合する方法である。
上記の方法は、トレツドゴム自体の粘着性が
良好で貼合作業も容易であり、かつ、加硫後のス
プライス部接着力も十分に高く問題ないが、用い
るゴムがNR又はIRに限定されるという欠点があ
る。
また、上記の方法では、トレツドゴム自体の
貼着性が乏しいため、粘着性および加硫接着性に
優れたゴムセメント(トレツドスプライスセメン
ト、以下、スプライスセメントという)を接合部
両面に塗布する必要がある。このスプライスセメ
ントとしては、通常のトレツドゴム配合の場合に
は、該トレツドゴム配合と類似した配合であつて
タツキフアイヤー等の粘着付与剤を多用したセメ
ントが有効である。しかし、特定のトレツドゴム
配合、すなわち、結合スチレン含有量が使用ポリ
マーの30重量%を越えるような高スチレン量のト
レツドゴムでは、スプライスセメントを接合部両
面に塗布すると接合面への良好な粘着性は付与で
きるものの加硫後のスプライス接着力が低下し、
走行中にトレツドスプライス部が剥がれるという
問題がある。
〔発明の目的〕
本発明は、高スチレンゴムを主要ポリマーとす
るタイヤトレツドのスプライス面に良好な粘着性
と優れた加硫接着性とを付与し得るタイヤ成形方
法を提供することを目的とする。
〔発明の構成〕
このため、本発明は、ポリマー総合計のうち30
重量%以上の結合スチレンを含むゴム組成物から
なる帯状物の一端と他端とを接合して環状のタイ
ヤトレツドとするに際し、100℃〜300℃に加熱し
た刃物で、一端は切断面と表面とのなす角度が他
端は切断面と底面とのなす角度が各々50度以下の
角度で、前記帯状物の両端部をそれぞれ横断的に
切断して接合面を形成させ、ついで、これらの接
合面同士を60分間以内に貼合することを特徴とす
るタイヤ成形方法を要旨とするものである。
以下、本発明の構成について詳しく説明する。
本発明におけるポリマー総合計のうち30重量%
以上の結合スチレンを含むゴム組成物(複数のポ
リマーが使用されている場合には、その結合スチ
レン含量の合計が30重量%以上)は、例えば、結
合スチレン含量30重量%以上のSBRにカーボン
ブラツク、オイル、その他の配合剤を配合してな
るものである。このようなゴム組成物からなるタ
イヤトレツドは、どのような種類のゴムセメント
を用いても又は該ゴム組成物と同一配合の配合物
をセメント化したものを用いても加硫後のスプラ
イス部接着力が非スプライス部の破断強力に比べ
て大幅に低下してしまう。
本発明では、このようなゴム組成物からなる帯
状物の一端と他端とを接合して環状のタイヤトレ
ツドとするに際して、まず、100℃〜300℃に加熱
した刃物で、一端は切断面と表面とのなす角度が
他端は切断面と底面とのなす角度が各々50度以下
の角度で、該帯状物の両端部をそれぞれ横断的に
切断して接合面を形成されるのである。上記ゴム
組成物は結合スチレン含有率が高いことから、未
加硫トレツドゴムが固く、タツク(粘着性)も乏
しい傾向にある。そこで、加熱した刃物でこれを
切断し、新鮮なスプライス面を形成させると、刃
物の熱によつて表層ゴムが柔化し、同時にブルー
ム物が除去されることからタツクが成形作業には
十分な水準まで向上することになる。この場合、
刃物の温度が重要であり、100℃以上300℃未満、
好ましくは200〜250℃である。100℃未満ではト
レツドを変形させずに容易に切断するのが困難で
あり、また、300℃を越えるとゴムが刃との接触
で容易に分解、炭化して逆に接着性とタツクを低
下させてしまう。切断は、若干長めに切つておい
た帯状物の端末を該帯状物の上下面に対して縦、
横のいずれの方向からでも行つてもよく、また、
予め長く巻き取つた帯状物を順次切取ることもで
きる。切断面と表面とのなす角度および切断面と
底面とのなす角度は、それぞれ50度以下でなけれ
ばならない。50度より大きい角度で切断、貼合し
た場合には、加硫中に金型とブラダーとによつて
発生する貼合面に垂直なプレス圧力、すなわち接
着圧力が低下してしまい、十分に高いスプライス
部接着力が得られないためである。
つぎに、本発明では、上記のようにして形成し
た接合面同士を60分間以内に貼合するのである。
この貼合は、ゴムセメントなどを用いることなく
そのまま行えばよい。60分間以内としたのは、切
断後60分を過ぎた頃に表面にブルーム物が増加
し、タツクが低下すると共に加硫後のスプライス
部接着力も通常の低い水準にまで低下するからで
ある。このため、貼合は、切断後60分間以内でで
きるだけ速やかに行うことが好ましい。
このように貼合した後、加硫を行うことにより
製品とすることができる。
以下に実施例および比較例を示す。なお、配合
割合は特記しない限り重量部を表わす。
実施例、比較例
(1) 実施例1〜3、比較例1〜4
下記表−1に示す配合−1からなるゴム組成物
をロール、チユーバーを用いる通常の押出し方法
にて押出して未加硫帯状物を作製した。ついで、
これを下記表−2に示す各種の条件で切断した後
成形、加硫し、タイヤサイズ225/515−13のレー
シングスリツクタイヤを作製した。これらのタイ
ヤについて、諸性能を評価した。この結果を表−
2に示す。なお、スプライス部の接着力は、サー
キツト走行後のスプライス部の状態およびタイヤ
から切り出したJIS3号ダンベル試験片の引張試験
の結果から判定した。
表−1(配合−1)
ハイスチレンSBR*1 137.5
SAF級カーボンブラツク 120
3号亜鉛華 5
ステアリン酸 2
老化防止剤*2 2
芳香族系オイル 82.5
イオウ 2.5
加硫促進剤*3 1.5
(註)
*1 結合スチレン含有率35重量%のコールド
タイプ乳化重合SBR、油37.5重量部の油展品。
*2 N−1,3−ジメチルブチル−N′−フ
エニル−p−フエニレンジアミン。
*3 N−シクロヘキシル−2−ベンゾチアゾ
ールスルフエンアミド。
[Technical Field of the Invention] The present invention relates to a tire molding method that improves the adhesion of the splice surface (joint surface) of a tire tread. [Prior Art] Conventionally, there are roughly two types of methods for tire tread splicing when one end and the other end of a belt-shaped article made of a rubber composition are joined to form an annular tire tread. That is, it is carried out using a tread mainly made of natural rubber (NR) or isoprene rubber (IR), in which a strip extruded from an extrusion molding machine is cut crosswise on a bias with a cutter to form a splice surface. A method of bonding splice surfaces as they are, and styrene
This is done using a tread made mainly of butadiene copolymer rubber (SBR) or butadiene rubber (BR), and the splice surface formed by cutting the extruded strip on a bias crosswise with a cutter has excellent adhesion. This method involves applying rubber cement, drying it, and then laminating it. In the above method, the adhesiveness of the tored rubber itself is good and the lamination work is easy, and the adhesive strength of the splice part after vulcanization is sufficiently high and there is no problem, but the disadvantage is that the rubber used is limited to NR or IR. There is. In addition, in the above method, since the adhesion of the treaded rubber itself is poor, it is necessary to apply rubber cement (treaded splice cement, hereinafter referred to as splice cement), which has excellent adhesiveness and vulcanization adhesion, to both sides of the joint. be. In the case of a conventional tored rubber compound, a cement having a similar formulation to the tored rubber compound and containing a large amount of tackifier such as tackifier is effective as the splice cement. However, in certain treaded rubber formulations, i.e. high styrene treaded rubbers where the bound styrene content exceeds 30% by weight of the polymer used, splice cement applied to both sides of the joint may provide good adhesion to the joint surfaces. Although it can be done, the splice adhesive strength after vulcanization decreases,
There is a problem with the tread splice part peeling off while driving. [Object of the Invention] An object of the present invention is to provide a tire molding method capable of imparting good tackiness and excellent vulcanization adhesion to the splice surface of a tire tread whose main polymer is high styrene rubber. [Configuration of the Invention] Therefore, the present invention provides that 30 out of the total polymer
When joining one end and the other end of a strip made of a rubber composition containing bound styrene in a weight percent or more to form an annular tire tread, one end is bonded to the cut surface and the surface using a knife heated to 100°C to 300°C. At the other end, the angle between the cut surface and the bottom surface is 50 degrees or less, and both ends of the strip are cut transversely to form a joint surface, and then these joint surfaces are The gist of this is a tire molding method characterized by bonding the tires together within 60 minutes. Hereinafter, the configuration of the present invention will be explained in detail. 30% by weight of the total polymer in the present invention
Rubber compositions containing the above bound styrene (if multiple polymers are used, the total bound styrene content is 30% by weight or more), for example, carbon black in SBR with a bound styrene content of 30% by weight or more. , oil, and other ingredients. Tire treads made of such rubber compositions have excellent splice adhesive strength after vulcanization, regardless of what kind of rubber cement is used or cemented with the same composition as the rubber composition. The breaking strength is significantly lower than that of the non-splice part. In the present invention, when joining one end and the other end of a strip made of such a rubber composition to form an annular tire tread, first, a blade heated to 100°C to 300°C is used to join one end to the cut surface and the other end. At the other end, the angle between the cut surface and the bottom surface is 50 degrees or less, and both ends of the strip are cut transversely to form a joint surface. Since the above-mentioned rubber composition has a high content of bound styrene, the unvulcanized tread rubber tends to be hard and have poor tackiness. Therefore, by cutting this with a heated knife to form a fresh splice surface, the surface rubber is softened by the heat of the knife, and at the same time, the blooming material is removed, so the tack is at a level sufficient for forming work. It will improve to. in this case,
The temperature of the cutlery is important, 100℃ or higher and lower than 300℃,
Preferably it is 200-250°C. At temperatures below 100°C, it is difficult to easily cut the tread without deforming it, and at temperatures above 300°C, the rubber easily decomposes and carbonizes on contact with the blade, conversely reducing its adhesion and tack. I end up. To cut, cut the slightly longer end of the strip vertically against the top and bottom surfaces of the strip.
You can go from either side, and
It is also possible to sequentially cut off a long strip that has been wound up in advance. The angle between the cut surface and the surface and the angle between the cut surface and the bottom surface must each be 50 degrees or less. When cutting and laminating at an angle greater than 50 degrees, the press pressure perpendicular to the laminating surface, that is, the adhesion pressure generated by the mold and bladder during vulcanization, decreases and is not sufficiently high. This is because adhesive strength at the splice portion cannot be obtained. Next, in the present invention, the bonding surfaces formed as described above are bonded together within 60 minutes.
This lamination may be performed as is without using rubber cement or the like. The reason why the time limit is within 60 minutes is because after 60 minutes after cutting, blooms increase on the surface and the tack decreases, as well as the adhesive strength of the splice after vulcanization also decreases to a normal low level. For this reason, it is preferable that the bonding be performed as soon as possible within 60 minutes after cutting. After laminating in this manner, a product can be obtained by vulcanization. Examples and comparative examples are shown below. It should be noted that the blending ratios are expressed in parts by weight unless otherwise specified. Examples, Comparative Examples (1) Examples 1 to 3, Comparative Examples 1 to 4 A rubber composition consisting of formulation 1 shown in Table 1 below was extruded using a normal extrusion method using a roll or a tuber to form an unvulcanized product. A strip was produced. Then,
This was cut under various conditions shown in Table 2 below, molded and vulcanized to produce racing slick tires with tire sizes of 225/515-13. Various performances of these tires were evaluated. Table this result.
Shown in 2. The adhesive strength of the splice portion was determined from the condition of the splice portion after running on the circuit and the results of a tensile test using a JIS No. 3 dumbbell test piece cut from the tire. Table-1 (Composition-1) High styrene SBR*1 137.5 SAF grade carbon black 120 No. 3 zinc white 5 Stearic acid 2 Anti-aging agent*2 2 Aromatic oil 82.5 Sulfur 2.5 Vulcanization accelerator*3 1.5 (Note) *1 Cold type emulsion polymerized SBR with bound styrene content of 35% by weight, oil-extended product with 37.5 parts by weight of oil. *2 N-1,3-dimethylbutyl-N'-phenyl-p-phenylenediamine. *3 N-cyclohexyl-2-benzothiazole sulfenamide.
【表】
以上の結果から、高スチレン量のSBRトレツ
ドゴムのスプライス部の接合は、従来通りセメン
トを接合面に塗布すると切断方法によらずタツク
は良好であるか加硫後の接着力が低下すること、
また、加熱した刃で切断する場合でも切断角度が
過度に大きかつたり、切断後の放置時間が長かつ
たりすると加硫後の接着力が低下することが判
る。
一方、本発明の条件を満たす例では、タツク、
加硫接着共に良好で、実用性に優れていることが
判る。
(2) 実施例4〜5、比較例5〜10
表−3に示す各種の結合スチレン含量の異なる
配合のトレツドゴムを用いて、実施例1〜3と同
様の試験を行つた。この結果を表−4に示す。な
お、表−3におけるSBR(スチレン23.5%、40%)
はいずれも乳化重合コールドタイプのSBRであ
り、他の配合剤は表−1に示したものと同一であ
る。[Table] From the above results, when joining splices of SBR tored rubber with a high styrene content, if cement is applied to the joint surface as before, the tack will be good regardless of the cutting method, or the adhesive force after vulcanization will decrease. thing,
Furthermore, even when cutting with a heated blade, if the cutting angle is too large or if the time after cutting is left for a long time, the adhesive strength after vulcanization decreases. On the other hand, in an example that satisfies the conditions of the present invention, tack,
It can be seen that both the vulcanization adhesion is good and the product is excellent in practicality. (2) Examples 4 to 5, Comparative Examples 5 to 10 The same tests as in Examples 1 to 3 were conducted using various tread rubbers with different bound styrene contents shown in Table 3. The results are shown in Table 4. In addition, SBR in Table 3 (styrene 23.5%, 40%)
Both are emulsion polymerized cold type SBR, and the other ingredients are the same as those shown in Table 1.
【表】【table】
以上説明したように本発明の方法によれば、セ
メントを塗布する従来技術では十分に強固な接着
が得られなかつた高スチレンSBR(結合スチレン
含量30重量%以上)を主体とするトレツドゴムの
スプライス部を非スプライス部の破断強度と同程
度に強固に接着させることができる。したがつ
て、本発明は、高スチレンSBRを多用する高グ
リツプタイヤやサーキツト走行を目的とするレー
シングタイヤ等のトレツドのスプライス部の接合
に効果的に利用可能である。
As explained above, according to the method of the present invention, a splice part of a treaded rubber mainly made of high styrene SBR (bonded styrene content of 30% by weight or more), for which sufficiently strong adhesion could not be obtained using the conventional technique of applying cement, can be achieved. can be bonded as strongly as the breaking strength of the non-splice portion. Therefore, the present invention can be effectively used for joining splices of treads of high grip tires that use a large amount of high styrene SBR, racing tires intended for circuit driving, and the like.
Claims (1)
チレンを含むゴム組成物からなる帯状物の一端と
他端とを接合して環状のタイヤトレツドとするに
際し、100℃〜300℃に加熱した刃物で、一端は切
断面と表面とのなす角度が他端は切断面と底面と
のなす角度が各々50度以下の角度で、前記帯状物
の両端部をそれぞれ横断的に切断して接合面を形
成させ、ついで、これらの接合面同士を60分間以
内に貼合することを特徴とするタイヤ成形方法。1. When joining one end and the other end of a strip made of a rubber composition containing bound styrene in an amount of 30% or more by weight of the total polymer to form an annular tire tread, use a knife heated to 100°C to 300°C, At one end, the angle between the cut surface and the surface is 50 degrees or less, and at the other end, the angle between the cut surface and the bottom surface is each 50 degrees or less, and both ends of the strip are cut transversely to form a joint surface. , and then bonding these bonded surfaces together within 60 minutes.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP61030680A JPS62189149A (en) | 1986-02-17 | 1986-02-17 | Molding of tire |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP61030680A JPS62189149A (en) | 1986-02-17 | 1986-02-17 | Molding of tire |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS62189149A JPS62189149A (en) | 1987-08-18 |
| JPH0348025B2 true JPH0348025B2 (en) | 1991-07-23 |
Family
ID=12310410
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP61030680A Granted JPS62189149A (en) | 1986-02-17 | 1986-02-17 | Molding of tire |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS62189149A (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2887815B2 (en) * | 1990-08-08 | 1999-05-10 | アイシン精機株式会社 | Mobile station position monitoring system |
| JP2003103654A (en) * | 2001-09-28 | 2003-04-09 | Yokohama Rubber Co Ltd:The | Tire molding method |
| JP2010162997A (en) * | 2009-01-14 | 2010-07-29 | Yokohama Rubber Co Ltd:The | Pneumatic tire and method of manufacturing the same |
| JP7255177B2 (en) | 2018-12-27 | 2023-04-11 | セイコーエプソン株式会社 | Recording device and recording device management method |
-
1986
- 1986-02-17 JP JP61030680A patent/JPS62189149A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS62189149A (en) | 1987-08-18 |
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