JPH0115404B2 - - Google Patents
Info
- Publication number
- JPH0115404B2 JPH0115404B2 JP57078199A JP7819982A JPH0115404B2 JP H0115404 B2 JPH0115404 B2 JP H0115404B2 JP 57078199 A JP57078199 A JP 57078199A JP 7819982 A JP7819982 A JP 7819982A JP H0115404 B2 JPH0115404 B2 JP H0115404B2
- Authority
- JP
- Japan
- Prior art keywords
- rubber
- weight
- parts
- properties
- tires
- 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
Links
- 229920001971 elastomer Polymers 0.000 claims description 68
- 239000005060 rubber Substances 0.000 claims description 68
- 239000000203 mixture Substances 0.000 claims description 31
- 239000004606 Fillers/Extenders Substances 0.000 claims description 17
- 229920003048 styrene butadiene rubber Polymers 0.000 claims description 13
- 229920001194 natural rubber Polymers 0.000 claims description 10
- 230000005484 gravity Effects 0.000 claims description 9
- 244000043261 Hevea brasiliensis Species 0.000 claims description 7
- 229920003052 natural elastomer Polymers 0.000 claims description 7
- 239000006229 carbon black Substances 0.000 claims description 6
- 229920002857 polybutadiene Polymers 0.000 claims description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 33
- 239000003921 oil Substances 0.000 description 21
- 230000000052 comparative effect Effects 0.000 description 14
- 230000007423 decrease Effects 0.000 description 14
- 238000002156 mixing Methods 0.000 description 14
- 239000004636 vulcanized rubber Substances 0.000 description 8
- 229910052799 carbon Inorganic materials 0.000 description 7
- 230000000704 physical effect Effects 0.000 description 7
- 239000002174 Styrene-butadiene Substances 0.000 description 6
- 238000005299 abrasion Methods 0.000 description 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- 238000004073 vulcanization Methods 0.000 description 4
- 239000005062 Polybutadiene Substances 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 239000010692 aromatic oil Substances 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 238000013329 compounding Methods 0.000 description 2
- 230000008094 contradictory effect Effects 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 239000012153 distilled water Substances 0.000 description 2
- 230000020169 heat generation Effects 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-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
- 230000003712 anti-aging effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 230000005012 migration Effects 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
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000010690 paraffinic oil Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000012779 reinforcing material Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000007665 sagging Methods 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- 239000000661 sodium alginate Substances 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
- 239000001993 wax Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B60—VEHICLES IN GENERAL
- B60C—VEHICLE TYRES; TYRE INFLATION; TYRE CHANGING; CONNECTING VALVES TO INFLATABLE ELASTIC BODIES IN GENERAL; DEVICES OR ARRANGEMENTS RELATED TO TYRES
- B60C1/00—Tyres characterised by the chemical composition or the physical arrangement or mixture of the composition
- B60C1/0016—Compositions of the tread
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Tires In General (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Description
本発明は、重荷重車両タイヤ用トレツドゴム組
成物に関し、更に詳しくは、雪上氷上路面におけ
る制動性能および湿潤路面における制動性能が良
好で、しかも一般路面用タイヤ、特にラグタイヤ
として耐摩耗性が耐カツトチツピング性にも優れ
た、トラツク・バス等比較的大型車両に使用され
る重荷重車両タイヤ用トレツドゴム組成物に関す
る。
従来、トラツク・バス等比較的大型車両に使用
されるタイヤ(以下トラツク・バス用タイヤとい
う)は雪上氷上路面における制動性能(以下、ア
イススキツド性という)に優れた冬用タイヤ、い
わゆるスノータイヤと、耐摩耗性および湿潤路面
における制動性能(以下、ウエツトスキツド性と
いう)に優れた一般路面用タイヤとが、季節によ
り使い分けられてきた。すなわち、従来技術にお
いては、スノータイヤ等雪上氷上路面で使用され
る冬用タイヤ用トレツドゴム組成物と、湿潤路面
で使用される一般路面用タイヤ用トレツドゴム組
成物とは、上記のような異なつた性能を要求され
るために、それぞれ異なつたゴム組成物を使用す
るのが常套手段であつた。従つて氷雪地域の使用
者は、スノータイヤと一般タイヤの2種類のタイ
ヤを必要に応じ使いわける不便さを甘受しなけれ
ばならなかつた。
結局、耐摩耗性やウエツトスキツド性を有する
トレツドゴムにアイススキツド性を付与させるこ
とは、ウエツトスキツド性や操縦安定性の面で性
能低下をきたし、両者の特性を満足するトレツド
ゴムを得ることは困難であつた。
また、この様なトレツドゴムの不備を補うべ
く、トレツドパターンとして全天候型ブロツクパ
ターン化への試みや、一般路面タイヤにチエーン
を装置して氷、雪上路面走行を行なつているが、
前者は、耐摩耗性低下および騒音問題を引き起こ
し、一方、後者は路面の破損に加えて騒音問題が
更に助長されるばかりでなく、公道上で脱着を行
なう場合、安全性の面で大変危険を伴なう他、チ
エーンによるトレツドゴムへの外傷を引き起こし
かねないという危険性がある。
それ故、一般路面タイヤに耐摩耗性やウエツト
スキツド性の他、トラツク・バス等比較的大型車
両として要求される耐カツト性、耐チツピング
性、耐疲労性を兼備し、かつアイススキツド性の
優れたゴム材料および該ゴム材料を有する空気入
りタイヤが望まれていた。
そこで、耐摩耗性およびウエツトスキツド性等
の諸特性の優れたトレツドゴムにアイススキツド
性を付加させる方法がいくつか提案されている
が、未だ、満足した結果が得られていない。例え
ば、アルギン酸ナトリウム親和性付与剤をトレツ
ド用ゴム組成物に添加する方法(例えば、特開昭
52−152003号)や特定の粉末ゴムをトレツド用ゴ
ム組成物に配合する方法(例えば、特開昭53−
133248号)より得られるトレツドゴムでは、アイ
ススキツド性を付加すると、逆に、ウエツトスキ
ツド性を著しく低下させる。
又、原料ゴムの組成比を改良する方法として、
例えば、特開昭55−135149号、特開昭55−18388
号、特開昭54−50546号など)がある。しかしな
がら、特開昭55−135149号には、スチレン・ブタ
ジエン共重合体ゴム(SBR)と伸展油を多量に
配合することが提案されているが、カーボンブラ
ツクおよび伸展油の配合量が多過ぎるために過荷
重時にゴムのヘタリ(スマツシユ現象)や発熱に
伴なうトレツドゴムのはく離現象を誘発する恐れ
があるので、トラツク・バス用タイヤに使用する
には不適当である。又、特開昭55−18388号に開
示された天然ゴムを主体ゴムとした配合は、悪路
面用タイヤ、特にラグタイヤに使用するには、耐
カツトチツピング性に劣り、特開昭54−50546号
に開示された天然ゴム、SBRを主体ゴムとした
配合は、アイススキツド性とウエツトスキツド性
とのバランスが必ずしも満足できるものではな
い。
以上のように、トラツク・バス用に用いられる
アイススキツド性、ウエツトスキツド性、耐摩耗
性および耐カツトチツピング性等のすべての性能
に優れた空気入りタイヤは、いまだ満足すべきも
のが開発されていないのが現状である。
本発明の目的は、かかる要求に応じて、従来は
相反すると思われていたアイススキツド性とウエ
ツトスキツド性の両性能を満足し、かつ、悪路面
用タイヤ、特にラグタイヤとしての耐摩耗性およ
び耐カツトチツピング性をも満足し、特にトラツ
ク・バス用タイヤに要求される苛酷な条件を満足
する重荷重車両タイヤ用トレツドゴム組成物を提
供することにある。
本発明者は、上記目的に沿つて、天然ゴム
(NR)および/またはポリイソプレンゴム
(IR)、スチレン・ブタジエン共重合体ゴム
(SBR)およびポリブタジエンゴム(BR)の配
合比率、特にSBRの特性を生かすべく配合比率
を検討すると共に、伸展油の特性にも着目して鋭
意研究の結果、低温下でも流動性のある伸展油を
特定配合比率で用いられることにより、加硫ゴム
の粘弾性の低下を抑制できることを発見し、本発
明に到達した。
すなわち、本発明は、天然ゴムおよび/または
ポリイソプレンゴム30〜60重量部、ポリブタジエ
ンゴム5〜40重量部およびスチレンブタジエン共
重合体ゴム30〜60重量部よりなるゴム分100重量
部に対し、粘度比重恒数(V.G.C.)0.80〜0.93を
有する伸展油を5〜20重量部およびカーボンブラ
ツクを45〜60重量部配合した重荷重車両タイヤ用
トレツドゴム組成物にあり、該トレツドゴム組成
物が上記目的を満足するものである。
スチレン・ブタジエン共重合体ゴムは、一般路
面用タイヤの操縦安定性やウエツトスキツド性を
確保すると共に、悪路面用タイヤ(特にラグタイ
ヤ)に要求される耐カツトチツピング性を確保す
るためにも必要不可欠な成分であり、その配合比
率は、ゴム分中の30〜60重量部である。60重量部
を超えるとアイススキツド性が低下するだけでな
く、発熱が高くなりトレツドセパレーシヨンが誘
発する、又、30重量部未満では、ウエツトスキツ
ド性に劣る。スチレン含有量は、好ましくは25重
量%以下、特に18重量%以下が好ましい。スチレ
ン含有量が余りに多過ぎると、耐カツトチツピン
グ性は向上するが、逆にアイススキツド性が低下
する。
ポリブタジエンゴムは、耐摩耗性およびアイス
スキツド性を向上させるが、多量に配合すると、
破断強度物性、引裂特性の低下を誘発すると共
に、耐カツトチツピング性を著しく低下させ、逆
に余りに少なすぎると、アイススキツド性が著し
く低下する。そのため、本発明に用いるポリブタ
ジエンゴムの配合比率は、ゴム分中5〜40重量
部、好ましくは10〜40重量部である。
天然ゴムおよび/またはポリイソプレンゴム
は、ウエツトスキツド性とアイススキツド性との
バランスが他のポリマー成分よりは良いが、60重
量部を超えると、加硫ゴムの物性としては満足で
きてもウエツトスキツド性とアイススキツド性の
低下を招く。30重量部未満ではトラツク・バス等
の比較的大きい荷重を受けるタイヤにおいては、
セパレーシヨン性並びに物性の低下のために満足
できない。このため、配合量はゴム分中30〜60重
量部である。
本発明においては、特定の粘度比重恒数(V.
G.C.)を有する伸展油の配合比率を特定すること
が重要である。ウエツトスキツド性を向上させる
ために伸展油を多量に配合することは公知であ
る。しかし、余りにも多量に配合すると、伸展油
がトレツド部からタイヤの他の部位に移行し(い
わゆるオイルマイグレーシヨン)、他の補強材と
ゴムとの接着性を低下させると共に、ゴム自体の
物性の変化、すなわち、硬度変化、脆化特性の低
下(脆化温度の上昇)を引き起こすので、長時間
使用するトラツク・バス用タイヤに適用するには
不適当である。しかしながら、本発明のゴム組成
物に、本発明で特定する粘度比重恒数を有する伸
展油を用いることにより、ウエツトスキツド性お
よびアイススキツド性の両性能を改善した乗用車
用タイヤ用トレツドゴム組成物(30〜80重量部)
に比べて著しく低い配合量で、加硫後のゴムの硬
度変化および脆化特性の低下を抑制しつつウエツ
トスキツド性およびアイススキツド性の両性能を
改善することを可能とした。すなわち、本発明に
おける伸展油の配合比率は、ゴム分100重量部に
対して5〜20重量部である。20重量部を超える
と、加硫ゴムの物性としての強度の低下をもたら
し、カツト・チツピング性の低下をもたらすほ
か、スマツシング現象(ゴムの永久歪によりタイ
ヤ溝が小さくなる)を起こし耐摩耗性、ウエツト
スキツド性、アイススキツド性が低下する。一
方、5重量部未満では、加硫ゴムの物性は良くな
つても、ウエツトスキツド性やアイススキツド性
の低下を招くと共に、ゴムの加工性が悪くなる。
また、本発明に使用する伸展油は、あらかじめ
油展ゴム中に含まれるものも含めた伸展油の全量
に対し、30〜80重量%、好ましくは40〜80重量%
の伸展油は、粘度比重恒数(V.G.C.)が0.80〜
0.90の範囲にあり、かつ、流動点が−5℃以下、
好ましくは−10℃以下である石油系ゴム用軟化剤
等の炭化水素油を用いることが好ましい。したが
つて、全伸展油の下式(1)によつて計算される粘度
比重恒数(V.G.C.)は、0.80〜0.93、好ましくは
0.80〜0.92であることが必要である。
粘度比重恒数(V.G.C.)=0.00743CP+0.00925CN
+0.0110CA…(1)
(CP、CNおよびCAはそれぞれ、パラフイン炭素
百分率、ナフテン炭素百分率、芳香族百分率を表
わす)
アロマ系オイル、例えばV.G.C. 0.96のもので
はアイススキツド性を満足できず、パラフイン系
オイル、例えばV.G.C. 0.84のもの単独またはア
ロマ系オイルとの併用系が目的達成のため不可欠
となる。0.80未満ではウエツトスキツド性は満足
できず、さらにはゴムとの相溶性低下を引き起こ
し、ゴム物性が低下する。
本発明に使用するカーボンブラツクは、ゴム分
100重量部に対し、45〜60重量部である。カーボ
ンブラツクは、ウエツトスキツド性、耐摩耗性お
よび耐カツト性を向上させるが、70重量部を超え
て配合すると、耐カツトチツピング性および耐摩
耗性の低下を引き起こすばかりでなく、アイスス
キツド性を著しく低下させるので望ましくなく、
又、45重量部未満でも、耐摩耗性が低下するので
望ましくない。
なお、本発明のゴム組成物においては、前記し
たゴム分、伸展油、カーボンブラツクに加えて酸
化亜鉛、ステアリン酸、老化防止剤、ワツクス、
加硫促進剤、イオウ等の配合剤が適宜適量配合さ
れる。
以下に、実施例および比較例を挙げて本発明を
具体的に説明する。なお、表中の配合はすべて重
量部である。
実施例1〜5および比較例1〜2
第1表に示す配合でゴム分および各種配合剤を
B型バンバリーミキサーで4分間混合してゴム組
成物を調製した。このゴム組成物を148℃で30分
間加硫して加硫ゴムを調製した。この加硫ゴムの
特性を測定した結果を併せて第1表に示した。な
お加硫ゴム特性の評価において、粘度比重恒数
(V.G.C.)は、
V.G.C.=0.00743CP+0.00925CN+0.0110CA…(1)
(CP、CNおよびCAはそれぞれパラフイン系炭素
百分率、ナフテン系炭素百分率、および芳香族系
炭素百分率を表わす)で示されたものである。
JISスプリング硬さおよびJIS反撥弾性は、各温
度での恒温室内に1時間放置後測定した値であ
る。ウエツトスキツド抵抗は、25℃の槽内にてブ
リテイツシユ ポータブル スキツドテスターを
用い、路面にはセーフテイーウオーク(住友スリ
ーエム社製)を用い蒸留水にて湿潤路面を作り、
測定した値を比較例1を100とした指数表示で表
わし、数値が大きい程スキツド抵抗は大きい。ア
イススキツド抵抗は、−20℃の槽内で同様の装置
を用い、路面としてはガラス板上に蒸留水を用い
て厚さ2mmの氷結路面を作り、測定した値を同様
に比較例1を100とした指数表示で表わした。
The present invention relates to a tread rubber composition for tires for heavy-duty vehicles, and more specifically, it has good braking performance on snow and ice roads and good braking performance on wet roads, and has good wear resistance and cut chipping resistance as tires for general road use, especially lug tires. The present invention relates to a tread rubber composition for heavy-duty vehicle tires used for relatively large vehicles such as trucks and buses, which has excellent performance. Traditionally, tires used for relatively large vehicles such as trucks and buses (hereinafter referred to as truck and bus tires) are winter tires, so-called snow tires, that have excellent braking performance on snow and ice roads (hereinafter referred to as ice skid properties). General road tires, which have excellent wear resistance and braking performance on wet road surfaces (hereinafter referred to as wet skid properties), have been used depending on the season. That is, in the prior art, tread rubber compositions for winter tires such as snow tires used on snow and ice roads and tread rubber compositions for general road tires used on wet roads have different performances as described above. Because of the requirements, it has been common practice to use different rubber compositions. Therefore, users in icy and snowy areas have had to accept the inconvenience of having to use two types of tires, snow tires and regular tires, depending on their needs. In the end, imparting ice skid properties to a treaded rubber that has wear resistance and wet skid properties results in a decrease in performance in terms of wet skid properties and handling stability, and it has been difficult to obtain a tread rubber that satisfies both properties. In addition, in order to compensate for these deficiencies in tread rubber, attempts have been made to create an all-weather block pattern as a tread pattern, and chains have been installed on general road tires to drive on ice and snow.
The former causes a decrease in wear resistance and noise problems, while the latter not only damages the road surface but also exacerbates the noise problem, and is extremely dangerous in terms of safety when attaching and detaching on public roads. In addition to this, there is a risk that the chain may cause damage to the tread rubber. Therefore, in addition to abrasion resistance and wet skidding properties for general road tires, this rubber also has the cut resistance, chipping resistance, and fatigue resistance required for relatively large vehicles such as trucks and buses, and has excellent ice skidding properties. What is desired is a material and a pneumatic tire having the rubber material. Therefore, several methods have been proposed for adding ice skid properties to treaded rubber which has excellent properties such as abrasion resistance and wet skid properties, but satisfactory results have not yet been obtained. For example, a method of adding a sodium alginate affinity imparting agent to a rubber composition for toreading (for example,
No. 52-152003) or a method of blending a specific powdered rubber into a rubber composition for toreading (for example,
In the treaded rubber obtained from No. 133248), when ice skid properties are added, the wet skid properties are significantly reduced. In addition, as a method of improving the composition ratio of raw rubber,
For example, JP-A-55-135149, JP-A-55-18388
No., Japanese Patent Publication No. 54-50546, etc.). However, JP-A-55-135149 proposes blending a large amount of styrene-butadiene copolymer rubber (SBR) and extender oil, but the amount of carbon black and extender oil is too large. It is unsuitable for use in truck and bus tires because there is a risk of sagging of the rubber (smashing phenomenon) and peeling of the treaded rubber due to heat generation when overloaded. In addition, the compound mainly composed of natural rubber disclosed in JP-A-55-18388 has poor chipping resistance when used in tires for rough roads, especially lug tires, and is disclosed in JP-A-54-50546. The disclosed formulations in which natural rubber and SBR are the main rubbers do not necessarily provide a satisfactory balance between ice skid properties and wet skid properties. As mentioned above, pneumatic tires used for trucks and buses that have excellent performance in all aspects, such as ice skid properties, wet skid properties, abrasion resistance, and cut chipping resistance, have not yet been developed. It is. The object of the present invention is to meet these demands by satisfying both ice skid properties and wet skid properties, which were conventionally thought to be contradictory, and to provide wear resistance and cut chipping resistance as a tire for rough road surfaces, especially as a lug tire. It is an object of the present invention to provide a tread rubber composition for heavy-duty vehicle tires that also satisfies the following conditions and particularly satisfies the severe conditions required for truck and bus tires. In line with the above objectives, the present inventor has investigated the blending ratio of natural rubber (NR) and/or polyisoprene rubber (IR), styrene-butadiene copolymer rubber (SBR), and polybutadiene rubber (BR), and in particular the characteristics of SBR. In addition to considering the blending ratio to make the most of the properties, we also focused on the characteristics of the extender oil and conducted intensive research. By using an extender oil that is fluid even at low temperatures at a specific blending ratio, the viscoelasticity of vulcanized rubber can be improved. The present invention was achieved by discovering that the decrease can be suppressed. That is, the present invention provides a method for reducing viscosity based on 100 parts by weight of rubber consisting of 30 to 60 parts by weight of natural rubber and/or polyisoprene rubber, 5 to 40 parts by weight of polybutadiene rubber, and 30 to 60 parts by weight of styrene-butadiene copolymer rubber. A tread rubber composition for heavy duty vehicle tires, which contains 5 to 20 parts by weight of an extender oil having a specific gravity constant (VGC) of 0.80 to 0.93 and 45 to 60 parts by weight of carbon black, the tread rubber composition satisfying the above object. It is something to do. Styrene-butadiene copolymer rubber is an essential component for ensuring the handling stability and wet skidding properties of tires for general road surfaces, as well as the cut-chipping resistance required for tires for rough roads (especially lug tires). The blending ratio is 30 to 60 parts by weight in the rubber component. If it exceeds 60 parts by weight, not only the ice skidding property will be reduced, but also the heat generation will increase and tread separation will be induced, and if it is less than 30 parts by weight, the wet skidding property will be poor. The styrene content is preferably 25% by weight or less, particularly preferably 18% by weight or less. If the styrene content is too high, the cut chipping resistance will improve, but the ice skid resistance will decrease. Polybutadiene rubber improves abrasion resistance and ice skid properties, but when added in large amounts,
It induces a decrease in physical properties of breaking strength and tear properties, and also significantly decreases cut chipping resistance.On the other hand, if it is too small, ice skid properties are significantly decreased. Therefore, the blending ratio of the polybutadiene rubber used in the present invention is 5 to 40 parts by weight, preferably 10 to 40 parts by weight, based on the rubber content. Natural rubber and/or polyisoprene rubber has a better balance between wet skid properties and ice skid properties than other polymer components, but if it exceeds 60 parts by weight, the wet skid properties and ice skid properties may be poor even though the physical properties of the vulcanized rubber are satisfactory. It leads to a decline in sexuality. If it is less than 30 parts by weight, in tires that are subjected to relatively large loads such as trucks and buses,
Unsatisfactory due to deterioration in separation properties and physical properties. Therefore, the blending amount is 30 to 60 parts by weight based on the rubber content. In the present invention, a specific viscosity specific gravity constant (V.
It is important to specify the blending ratio of extender oil with GC). It is known to incorporate a large amount of extender oil in order to improve wet skidding properties. However, if it is added in too large a quantity, the extension oil will migrate from the tread to other parts of the tire (so-called oil migration), reducing the adhesion between other reinforcing materials and rubber, and impairing the physical properties of the rubber itself. This causes a change in hardness, a decrease in embrittlement properties (increase in embrittlement temperature), and is therefore unsuitable for use in truck and bus tires that are used for long periods of time. However, by using an extender oil having a viscosity specific gravity constant specified in the present invention in the rubber composition of the present invention, a tread rubber composition for passenger car tires (30 to 80 parts by weight)
It is possible to improve both wet skid properties and ice skid properties while suppressing changes in hardness and deterioration of embrittlement properties of the rubber after vulcanization with a significantly lower blending amount than that of vulcanized rubber. That is, the blending ratio of the extender oil in the present invention is 5 to 20 parts by weight per 100 parts by weight of the rubber content. If it exceeds 20 parts by weight, the strength of the physical properties of the vulcanized rubber decreases, cutting and chipping properties decrease, and the smashing phenomenon (tire tread becomes smaller due to permanent deformation of the rubber) occurs, resulting in poor wear resistance. Wet skid properties and ice skid properties are reduced. On the other hand, if the amount is less than 5 parts by weight, even though the physical properties of the vulcanized rubber are improved, wet skid properties and ice skid properties are deteriorated, and the processability of the rubber is deteriorated. Further, the extender oil used in the present invention is 30 to 80% by weight, preferably 40 to 80% by weight, based on the total amount of extender oil including that already contained in the oil-extended rubber.
The extension oil has a viscosity specific gravity constant (VGC) of 0.80~
in the range of 0.90, and the pour point is -5℃ or less,
It is preferable to use a hydrocarbon oil such as a softener for petroleum-based rubber, which preferably has a temperature of −10° C. or lower. Therefore, the viscosity specific gravity constant (VGC) of the fully extended oil calculated by the following formula (1) is 0.80 to 0.93, preferably
It needs to be between 0.80 and 0.92. Viscosity specific gravity constant (VGC) = 0.00743C P +0.00925C N
+0.0110C A ...(1) (C P , C N and C A represent the paraffin carbon percentage, naphthenic carbon percentage, and aromatic percentage, respectively) Aromatic oils, such as those with VGC 0.96, cannot satisfy the ice skid property. , paraffinic oils such as VGC 0.84 alone or in combination with aromatic oils are essential to achieve the objective. If it is less than 0.80, the wet skid property will not be satisfactory, and furthermore, the compatibility with the rubber will decrease, and the physical properties of the rubber will deteriorate. The carbon black used in the present invention has a rubber content.
The amount is 45 to 60 parts by weight per 100 parts by weight. Carbon black improves wet skid properties, abrasion resistance, and cut resistance, but if it is added in an amount exceeding 70 parts by weight, it not only causes a decrease in cut chipping resistance and abrasion resistance, but also significantly reduces ice skid properties. undesirable;
Further, if the amount is less than 45 parts by weight, it is also undesirable because the wear resistance decreases. In addition, in the rubber composition of the present invention, in addition to the above-mentioned rubber component, extender oil, and carbon black, zinc oxide, stearic acid, an antiaging agent, wax,
Compounding agents such as a vulcanization accelerator and sulfur are blended in appropriate amounts. The present invention will be specifically explained below with reference to Examples and Comparative Examples. All formulations in the table are parts by weight. Examples 1 to 5 and Comparative Examples 1 to 2 Rubber compositions were prepared by mixing rubber components and various compounding agents in a B-type Banbury mixer for 4 minutes according to the formulations shown in Table 1. This rubber composition was vulcanized at 148° C. for 30 minutes to prepare a vulcanized rubber. The results of measuring the properties of this vulcanized rubber are also shown in Table 1. In the evaluation of vulcanized rubber properties, the viscosity specific gravity constant (VGC) is VGC=0.00743C P +0.00925C N +0.0110C A ...(1) (C P , C N and C A are each the paraffinic carbon percentage , naphthenic carbon percentage, and aromatic carbon percentage). JIS spring hardness and JIS rebound resilience are values measured after being left in a constant temperature room for 1 hour at each temperature. Wet skid resistance was measured by using a British portable skid tester in a tank at 25°C, and using Safety Walk (manufactured by Sumitomo 3M) to make a wet road surface with distilled water.
The measured values are expressed as an index with Comparative Example 1 set as 100, and the larger the value, the greater the skid resistance. The ice-skipped resistance was measured using a similar device in a tank at -20°C, using distilled water on a glass plate to create an icy road surface with a thickness of 2 mm, and comparing the measured value with Comparative Example 1 as 100. It is expressed as an index.
【表】【table】
【表】
第1表より明らかなように、実施例1〜5で表
わされる本発明のゴム組成物の加硫特性は、一般
路面用タイヤに要求されるJIS反撥弾性を備える
と同時に、高いウエツトスキツド抵抗を維持しな
がらアイススキツド抵抗を向上させた優れたゴム
組成物である。これに比較して、比較例1のゴム
組成物は、スチレン・ブタジエン共重合体ゴム
(SBR)の配合比率が低く、そのためにウエツト
スキツド抵抗に劣る。又、比較例2のゴム組成物
はキヤツプトレツド用の通常の配合で、耐カツト
性向上のためにホワイトカーボンが配合されてい
るが、スチレン・ブタジエン共重合体ゴム
(SBR)の配合比率が低く、しかも、ポリブタジ
エンゴム(BR)を含有しないために、ウエツト
スキツド抵抗とアイススキツド抵抗のバランスが
非常に悪い。更に、本発明で特定する粘度比重恒
数(V.G.C.)0.80〜0.93の伸展油を使用すること
により、従来の伸展油を用いた比較例1および比
較例2より多量の伸展油を用いるにもかかわら
ず、脆化温度は非常に低く、低温特性に優れ、か
つ、(−20℃)〜(50℃)における硬度変化も低
く抑制できる。
この実施例1〜5および比較例1〜2の試験結
果から、全伸展油のV.G.C.の値が0.80〜0.93のゴ
ム組成物において、加硫後の特性が、
(1) −20℃でのJISスプリング硬さ:70未満
(2) −20℃から50℃に至るJISスプリング硬さの
変化量:10ポイント以内
(3) 80℃におけるJIS反撥弾性:65%以下
(4) 0℃におけるJIS反撥弾性:35%以上40%以
下
(5) 脆化温度:−65℃以下好ましくは−70℃以下
であるゴム組成物が雪上・氷上路面及び湿潤路面
等の一般路面の両方の路面における運動性能をバ
ランス良く満足させるために必要となるという知
見を得た。
実施例6および比較例3〜4
実施例1、比較例1および比較例2の各ゴム組
成物をそれぞれトレツドに配置した空気入りタイ
ヤ(タイヤサイズ1000−24 14PR)を作製して実
車試験を行ない、比較例4を100とした指数で結
果を第2表に示した。[Table] As is clear from Table 1, the vulcanization characteristics of the rubber compositions of the present invention shown in Examples 1 to 5 are such that they have the JIS rebound properties required for general road tires, as well as high wet skid resistance. This is an excellent rubber composition that improves ice skid resistance while maintaining resistance. In comparison, the rubber composition of Comparative Example 1 has a low blending ratio of styrene-butadiene copolymer rubber (SBR), and therefore has poor wet skid resistance. In addition, the rubber composition of Comparative Example 2 has a normal formulation for captreads, and white carbon is blended to improve cut resistance, but the blending ratio of styrene-butadiene copolymer rubber (SBR) is low; Moreover, since it does not contain polybutadiene rubber (BR), the balance between wet skid resistance and ice skid resistance is very poor. Furthermore, by using an extender oil with a viscosity specific gravity constant (VGC) of 0.80 to 0.93 specified in the present invention, even though a larger amount of extender oil is used than in Comparative Examples 1 and 2, which used conventional extender oils. First, it has a very low embrittlement temperature, has excellent low-temperature properties, and can suppress changes in hardness between (-20°C) and (50°C). From the test results of Examples 1 to 5 and Comparative Examples 1 to 2, it was found that in rubber compositions in which the VGC value of the total extender oil is 0.80 to 0.93, the properties after vulcanization are (1) JIS at -20℃ Spring hardness: less than 70 (2) Change in JIS spring hardness from -20℃ to 50℃: within 10 points (3) JIS rebound at 80℃: 65% or less (4) JIS rebound at 0℃ : 35% or more and 40% or less (5) Brittleness temperature: -65°C or lower, preferably -70°C or lower The rubber composition balances the driving performance on both snow/ice roads and general roads such as wet roads. We have obtained the knowledge that it is necessary to achieve good satisfaction. Example 6 and Comparative Examples 3 to 4 Pneumatic tires (tire size 1000-24 14PR) were prepared in which each of the rubber compositions of Example 1, Comparative Example 1, and Comparative Example 2 were arranged on the tread, and an actual vehicle test was conducted. The results are shown in Table 2 as an index with Comparative Example 4 as 100.
【表】【table】
【表】
雪上氷上制動試験は、札幌市効外において−10
℃で平坦な圧雪路面を60Km/HRで走行し制動を
かけた時の制動距離で評価し、雪上氷上登坂試験
は、平均勾配7゜の坂道を200m、初速20Km/HRで
登坂した時に要する時間で評価した。又、湿潤路
面制動試験は、散水したテスト路面を60Km/HR
で走行し、制動をかけた際の制動距離で評価し
た。摩耗寿命は、悪路面を50%以上含むダンプト
ラツクを走行する際のタイヤ摩耗厚1mm当りの走
行距離で評価し、耐カツトチツピング性は、トレ
ツド部のカツトとチツピングの数によつて評価し
た。
第2表から明らかなように、比較例1のゴム組
成物を雪上氷上路面用タイヤのトレツドに配置す
ることによつて、アイススキツド性を付加する
と、ウエツトスキツド性が低下するばかりでな
く、耐摩耗性や耐カツトチツピング性が著しく低
下する(比較例3)。これに反して、実施例1で
得られた本発明のゴム組成物をトレツドに配置し
たタイヤ(実施例6)は、一般路面用タイヤにも
かかわらず、アイススキツド性に優れる。又、耐
摩耗性が高く、ウエツトスキツド性等その他の特
性も損われないため、悪路を走行したり、長時間
走行するトラツク・バス等比較的大型車両用タイ
ヤとして、特に有効であることも判明した。
以上の結果から、本発明のゴム組成物をトレツ
ドに配置する空気入りタイヤは、雪上氷上路面に
おける制動性能と湿潤路面における制動性能とい
う従来は相反すると思われていた2つの性能を満
足し、且つ、一般路面用タイヤの耐久性としての
耐摩耗性や耐カツトチツピング性をも満足させる
ことにより、1つのタイヤでいかなる路面でも走
行を可能にし、且つ、安全性の確保のほか路面の
損傷、騒音、タイヤ・チエーンの脱着に要する経
費の削減にも大きく貢献するものである。[Table] Braking test on snow and ice was -10 outside of Sapporo City.
Evaluated by the braking distance when driving at 60km/HR on a flat, compacted snow road at ℃, and the time required to climb a slope with an average slope of 7° for 200m at an initial speed of 20km/HR. It was evaluated by In addition, the wet road braking test was conducted on a water-sprinkled test road at 60km/hr.
The vehicle was evaluated based on the braking distance when the vehicle was driven and the brakes were applied. Wear life was evaluated by the distance traveled per 1 mm of tire wear thickness when driving on a dump truck with a rough road surface of 50% or more, and cut and chipping resistance was evaluated by the number of cuts and chips in the tread portion. As is clear from Table 2, when adding ice skid properties by disposing the rubber composition of Comparative Example 1 on the tread of a tire for snow and ice, not only does the wet skid property deteriorate, but the wear resistance also decreases. and the chipping resistance is significantly reduced (Comparative Example 3). On the contrary, the tire (Example 6) in which the rubber composition of the present invention obtained in Example 1 was disposed in the tread had excellent ice skid properties even though it was a general road tire. In addition, it has been found to be particularly effective as a tire for relatively large vehicles such as trucks and buses that travel on rough roads or for long periods of time, as it has high wear resistance and other characteristics such as wet skid properties are not impaired. did. From the above results, a pneumatic tire in which the rubber composition of the present invention is disposed in the tread satisfies two performances that were conventionally thought to be contradictory: braking performance on snow and ice roads and braking performance on wet roads. By satisfying the wear resistance and chipping resistance of general road tires, it is possible to drive on any road surface with a single tire, and in addition to ensuring safety, it also reduces road damage, noise, and This also greatly contributes to reducing the cost required for attaching and detaching tires and chains.
Claims (1)
30〜60重量部、ポリブタジエンゴム5〜40重量部
およびスチレン・ブタジエン共重合体ゴム30〜60
重量部よりなるゴム分100重量部に対し、粘度比
重恒数(V.G.C.)0.80〜0.93を有する伸展油を5
〜20重量部およびカーボンブラツクを45〜60重量
部配合したことを特徴とする重荷重車両タイヤ用
トレツドゴム組成物。1 Natural rubber and/or polyisoprene rubber
30 to 60 parts by weight, 5 to 40 parts by weight of polybutadiene rubber, and 30 to 60 parts by weight of styrene-butadiene copolymer rubber.
5 parts by weight of an extender oil having a viscosity specific gravity constant (VGC) of 0.80 to 0.93 to 100 parts by weight of rubber.
A tread rubber composition for heavy-duty vehicle tires, characterized in that it contains ~20 parts by weight and 45 to 60 parts by weight of carbon black.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57078199A JPS58199203A (en) | 1982-05-12 | 1982-05-12 | Pneumatic tyre |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57078199A JPS58199203A (en) | 1982-05-12 | 1982-05-12 | Pneumatic tyre |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS58199203A JPS58199203A (en) | 1983-11-19 |
JPH0115404B2 true JPH0115404B2 (en) | 1989-03-17 |
Family
ID=13655334
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP57078199A Granted JPS58199203A (en) | 1982-05-12 | 1982-05-12 | Pneumatic tyre |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS58199203A (en) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0610280B2 (en) * | 1983-12-12 | 1994-02-09 | 株式会社ブリヂストン | Improved pneumatic tire suitable for snow and ice roads |
JPS6131442A (en) * | 1984-07-23 | 1986-02-13 | Japan Synthetic Rubber Co Ltd | Butadiene polymer rubber composition |
JPS61111804U (en) * | 1984-12-27 | 1986-07-15 | ||
JPS62104847A (en) * | 1985-10-31 | 1987-05-15 | Japan Synthetic Rubber Co Ltd | Oil-extended isoprene based rubber composition |
JPH0653833B2 (en) * | 1987-01-13 | 1994-07-20 | 横浜ゴム株式会社 | Rubber composition for tire tread |
JPH02308832A (en) * | 1989-05-25 | 1990-12-21 | Yokohama Rubber Co Ltd:The | Rubber composition for tire tread |
US5753365A (en) * | 1991-06-07 | 1998-05-19 | Bridgestone Corporation | Rubber composition and all season type pneumatic tires made from a rubber composition |
US5798009A (en) * | 1994-12-27 | 1998-08-25 | Bridgestone Corporation | Foamed rubber compositions for tires and pneumatic tire using the same |
JP3406105B2 (en) * | 1995-01-13 | 2003-05-12 | 横浜ゴム株式会社 | Pneumatic tire |
US5776991A (en) * | 1995-03-29 | 1998-07-07 | Bridgestone Corporation | Foamed rubber compositions for pneumatic tires and method of producing the same |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS55135149A (en) * | 1979-04-11 | 1980-10-21 | Yokohama Rubber Co Ltd:The | Tire tread rubber composition and tire produced therefrom |
-
1982
- 1982-05-12 JP JP57078199A patent/JPS58199203A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS55135149A (en) * | 1979-04-11 | 1980-10-21 | Yokohama Rubber Co Ltd:The | Tire tread rubber composition and tire produced therefrom |
Also Published As
Publication number | Publication date |
---|---|
JPS58199203A (en) | 1983-11-19 |
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