JP2010248338A - Rubber composition and tire using the same - Google Patents
Rubber composition and tire using the same Download PDFInfo
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- JP2010248338A JP2010248338A JP2009098069A JP2009098069A JP2010248338A JP 2010248338 A JP2010248338 A JP 2010248338A JP 2009098069 A JP2009098069 A JP 2009098069A JP 2009098069 A JP2009098069 A JP 2009098069A JP 2010248338 A JP2010248338 A JP 2010248338A
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- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
本発明は、ゴム組成物および該ゴム組成物を用いたタイヤに関し、特に、タイヤのトレッド部に使用した場合にタイヤのグリップ性を向上すると共に耐摩耗性の低下を抑制することが可能なゴム組成物および該ゴム組成物を用いたタイヤに関するものである。 The present invention relates to a rubber composition and a tire using the rubber composition, and in particular, a rubber capable of improving the grip of the tire and suppressing a decrease in wear resistance when used in a tread portion of the tire. The present invention relates to a composition and a tire using the rubber composition.
従来、転がり抵抗を低減した低燃費タイヤに用いるタイヤトレッド用ゴム組成物として、未加硫ゴムの粘度を下げて加工性を高めると共に、加硫ゴムの転がり抵抗を低減し且つ耐摩耗性を改良するために脂肪酸亜鉛塩からなる加工助剤1〜10重量部をジエン系ゴム100重量部に対して配合したゴム組成物が知られている(例えば、特許文献1参照)。 Conventionally, as a rubber composition for tire treads used in low fuel consumption tires with reduced rolling resistance, the viscosity of unvulcanized rubber is lowered to improve processability, and the rolling resistance of vulcanized rubber is reduced and the wear resistance is improved. Therefore, a rubber composition is known in which 1 to 10 parts by weight of a processing aid composed of a fatty acid zinc salt is blended with 100 parts by weight of a diene rubber (for example, see Patent Document 1).
しかし、上述のようなゴム組成物を用いた低燃費タイヤでは、転がり抵抗の低減を図ることはできるものの、転がり抵抗の低減に伴い十分なグリップ力を得られない恐れがあった。 However, in the fuel-efficient tire using the rubber composition as described above, although the rolling resistance can be reduced, there is a fear that sufficient grip force cannot be obtained as the rolling resistance is reduced.
そこで、十分なグリップ性能を有するタイヤを得るために、ゴム成分に対し、スピンドルオイル、アロマオイル、リキッドオイル等のオイルを可塑剤として配合したゴム組成物からなる軟化ゴムをトレッド部に用いてタイヤのグリップ性能を高めることが試みられている。 Therefore, in order to obtain a tire having sufficient grip performance, a tire using a soft rubber made of a rubber composition in which an oil such as spindle oil, aroma oil, liquid oil or the like is blended as a plasticizer with a rubber component is used for the tread portion. Attempts have been made to improve grip performance.
しかしながら、上述のような従来の可塑剤(オイル)を配合したゴム組成物をトレッド部に用いる場合、多量の可塑剤を配合してトレッドゴムを軟化させる(加硫ゴムのモジュラスを低減させる)ことでタイヤのグリップ性能を向上させることは可能であるものの、トレッドゴムの軟化によりタイヤの耐摩耗性が大幅に低下してしまうという問題があった。 However, when the rubber composition containing the conventional plasticizer (oil) as described above is used for the tread portion, the tread rubber is softened by adding a large amount of plasticizer (reducing the modulus of the vulcanized rubber). However, although it is possible to improve the grip performance of the tire, there has been a problem that the wear resistance of the tire is greatly lowered due to the softening of the tread rubber.
そのため、タイヤのトレッド部に用いた場合に、軟化による耐摩耗性の低減を抑制しつつタイヤのグリップ性能を向上させることが可能なゴム組成物が求められていた。また、該ゴム組成物を用いた、グリップ性能が高く、一定の耐摩耗性を有するタイヤが求められていた。 For this reason, there has been a demand for a rubber composition that can improve the grip performance of a tire while suppressing a reduction in wear resistance due to softening when used in a tread portion of a tire. There has also been a demand for a tire using the rubber composition that has high grip performance and constant wear resistance.
本発明者は、上記課題を解決するために鋭意検討した結果、ゴム成分に対して配合した場合に、従来の可塑剤と同様な加硫ゴムのモジュラス低減効果を得てタイヤのグリップ性能の向上を図ることが可能であり、且つ、従来の可塑剤を配合した場合と比較して破壊強力(TB)の低下を小さくすることが可能な物質として、脂肪酸金属塩を見出した。そして、従来ゴム成分に対し配合していた可塑剤(オイル)の一部を脂肪酸金属塩に代え、ゴム成分に対して所定量の脂肪酸金属塩および従来の可塑剤を配合してゴム組成物とすることにより、本発明を完成するに至った。 As a result of intensive studies to solve the above problems, the present inventor has improved the grip performance of the tire by obtaining the same modulus reduction effect of vulcanized rubber as that of a conventional plasticizer when blended with a rubber component. As a substance capable of reducing the decrease in breaking strength (TB) as compared with the case where a conventional plasticizer is added, a fatty acid metal salt has been found. Then, a part of the plasticizer (oil) conventionally blended with the rubber component is replaced with the fatty acid metal salt, and a predetermined amount of the fatty acid metal salt and the conventional plasticizer are blended with the rubber component to obtain a rubber composition. As a result, the present invention has been completed.
即ち、本発明のゴム組成物は、ゴム成分100質量部に対して、可塑剤50〜210質量部を配合したゴム組成物であって、前記可塑剤のうち1〜20質量部が脂肪酸金属塩よりなることを特徴とするものである。このように、配合する可塑剤の一部を脂肪酸金属塩とすることにより、タイヤのトレッド部に用いた場合にタイヤのグリップ性能の向上と耐摩耗性の低減の抑制との両立を達成することが可能な、加硫ゴムのモジュラス低減効果を得つつ耐摩耗性の低下を抑制したゴム組成物を得ることができる。なお、ゴム成分100質量部に対する可塑剤の配合量が50質量部未満の場合には、加硫ゴムのモジュラス低減効果が十分でなく、210質量部を超える場合には、耐摩耗性が低下し過ぎると共に転がり抵抗が大きくなり過ぎてしまう。また、可塑剤中の脂肪酸金属塩の量が1質量部未満の場合には、耐摩耗性の低減抑制効果が小さい。 That is, the rubber composition of the present invention is a rubber composition in which 50 to 210 parts by mass of a plasticizer is blended with 100 parts by mass of a rubber component, and 1 to 20 parts by mass of the plasticizer is a fatty acid metal salt. It is characterized by comprising. In this way, by using a fatty acid metal salt as a part of the plasticizer to be blended, achieving both improvement in tire grip performance and suppression of wear resistance reduction when used in the tread portion of the tire Thus, it is possible to obtain a rubber composition capable of suppressing the decrease in wear resistance while obtaining the effect of reducing the modulus of vulcanized rubber. In addition, when the compounding amount of the plasticizer with respect to 100 parts by mass of the rubber component is less than 50 parts by mass, the effect of reducing the modulus of the vulcanized rubber is not sufficient, and when it exceeds 210 parts by mass, the wear resistance decreases. As it passes, rolling resistance becomes too large. Moreover, when the amount of the fatty acid metal salt in the plasticizer is less than 1 part by mass, the effect of suppressing the reduction in wear resistance is small.
本発明のゴム組成物は、前記可塑剤のうち11〜20質量部が脂肪酸金属塩よりなることが好ましい。 In the rubber composition of the present invention, 11 to 20 parts by mass of the plasticizer is preferably composed of a fatty acid metal salt.
ここで、本発明のゴム組成物は、前記ゴム成分の少なくとも70質量%が、スチレン含有率が20〜60質量%、好ましくは31〜60質量%のスチレン−ブタジエン共重合ゴムからなることが好ましい。ゴム成分の少なくとも70質量%をスチレン含有率が20〜60質量%のスチレン−ブタジエン共重合ゴム(SBR)とすることにより、加硫ゴムのモジュラスをより低減し、且つ、耐摩耗性の低下をより抑制したゴム組成物を提供することができる。ここで、ゴム成分中のSBR量が70質量%未満の場合には、SBRの特性を十分に発揮させることができない。また、スチレン含有率が20質量%未満の場合には、十分なモジュラス低減効果を得ることができず、60質量%を超える場合には、転がり抵抗が大きくなり過ぎてしまう。なお、ゴム成分中のSBRは、1種のSBRのみからなっても良いし、スチレン含有率等が異なる複数種のSBRの混合物からなっても良い。 Here, in the rubber composition of the present invention, at least 70% by mass of the rubber component is preferably composed of a styrene-butadiene copolymer rubber having a styrene content of 20 to 60% by mass, preferably 31 to 60% by mass. . By using at least 70% by mass of the rubber component as a styrene-butadiene copolymer rubber (SBR) having a styrene content of 20 to 60% by mass, the modulus of the vulcanized rubber is further reduced and the wear resistance is reduced. A more suppressed rubber composition can be provided. Here, when the amount of SBR in the rubber component is less than 70% by mass, the characteristics of SBR cannot be exhibited sufficiently. Further, when the styrene content is less than 20% by mass, a sufficient modulus reduction effect cannot be obtained, and when it exceeds 60% by mass, the rolling resistance becomes too large. The SBR in the rubber component may be composed of only one type of SBR, or may be composed of a mixture of a plurality of types of SBR having different styrene contents.
本発明のゴム組成物は、前記スチレン−ブタジエン共重合ゴムのブタジエン部分のビニル含有率が30〜60質量%であることが好ましい。ブタジエン部分のビニル含有率が30質量%未満の場合には、十分なモジュラス低減効果を得ることができず、また、60質量%を超える場合には、転がり抵抗が大きくなり過ぎてしまうからである。 In the rubber composition of the present invention, the vinyl content of the butadiene portion of the styrene-butadiene copolymer rubber is preferably 30 to 60% by mass. This is because when the vinyl content of the butadiene portion is less than 30% by mass, a sufficient modulus reduction effect cannot be obtained, and when it exceeds 60% by mass, the rolling resistance becomes too large. .
本発明のゴム組成物は、ゴム成分100質量部に対して、カーボンブラック60〜200質量部を配合することが好ましい。 The rubber composition of the present invention preferably contains 60 to 200 parts by mass of carbon black with respect to 100 parts by mass of the rubber component.
また、本発明のタイヤは、少なくともトレッド部を上記のゴム組成物で構成したことを特徴とする。このように、タイヤのトレッド部を上記ゴム組成物で構成することにより、耐摩耗性を大幅に低減することなく、グリップ性能の高いタイヤを得ることができる。なお、トレッド部を上記ゴム組成物で構成するタイヤとしては、特に、レーシングタイヤを含む高性能タイヤが好ましい。 The tire of the present invention is characterized in that at least a tread portion is composed of the above rubber composition. Thus, by constituting the tread portion of the tire with the rubber composition, a tire with high grip performance can be obtained without significantly reducing the wear resistance. In addition, as a tire which comprises a tread part with the said rubber composition, the high performance tire containing a racing tire is especially preferable.
本発明によれば、従来の可塑剤の一部に代えて脂肪酸金属塩を用いることにより、加硫ゴムのモジュラス低減効果を得てタイヤのトレッド部に使用した場合にグリップ性を向上させることが可能であり、且つ、耐摩耗性の低減を抑制することも可能なゴム組成物を提供することができる。また、当該ゴム組成物を用いた、耐摩耗性を大幅に低減することなくグリップ性能を向上させたタイヤを提供することができる。 According to the present invention, by using a fatty acid metal salt instead of a part of a conventional plasticizer, it is possible to obtain a modulus reduction effect of vulcanized rubber and improve grip properties when used in a tread portion of a tire. It is possible to provide a rubber composition that is capable of suppressing wear resistance reduction. Moreover, the tire which improved the grip performance can be provided using the said rubber composition, without reducing abrasion resistance significantly.
<ゴム組成物>
以下に、本発明のゴム組成物を詳細に説明する。本発明に従うゴム組成物は、ゴム成分100質量部に対して、可塑剤50〜210質量部を配合したゴム組成物であって、可塑剤のうち1〜20質量部が脂肪酸金属塩よりなることを特徴とし、加硫ゴムのモジュラス低減効果を得つつ耐摩耗性の低下を抑制したものである。
<Rubber composition>
Below, the rubber composition of this invention is demonstrated in detail. The rubber composition according to the present invention is a rubber composition in which 50 to 210 parts by mass of a plasticizer is blended with 100 parts by mass of a rubber component, and 1 to 20 parts by mass of the plasticizer is composed of a fatty acid metal salt. It is characterized by suppressing the decrease in wear resistance while obtaining the effect of reducing the modulus of vulcanized rubber.
ここで、ゴム成分は、天然ゴム(NR)、合成ゴム、またはそれらを混合したものからなり、合成ゴムとしては、具体的には、スチレン−ブタジエン共重合ゴム(SBR)、ポリイソプレンゴム(IR)、ポリブタジエンゴム(BR)、ポリクロロプレンゴム(CR)、イソプレン−イソブチレン共重合ゴム(IIR)、アクリロニトリル−ブタジエン共重合ゴム(NBR)およびエチレン−プロピレン共重合ゴム(EPDM)等が挙げられる。 Here, the rubber component is composed of natural rubber (NR), synthetic rubber, or a mixture thereof. Specific examples of the synthetic rubber include styrene-butadiene copolymer rubber (SBR), polyisoprene rubber (IR). ), Polybutadiene rubber (BR), polychloroprene rubber (CR), isoprene-isobutylene copolymer rubber (IIR), acrylonitrile-butadiene copolymer rubber (NBR), and ethylene-propylene copolymer rubber (EPDM).
なお、ゴム成分は、少なくとも70質量%が、スチレン含有率が20〜60質量%であって且つブタジエン部分のビニル含有率が30〜60質量%であるスチレン−ブタジエン共重合ゴム(SBR)からなることが好ましい。 The rubber component is composed of a styrene-butadiene copolymer rubber (SBR) having at least 70% by mass, a styrene content of 20 to 60% by mass, and a vinyl content of the butadiene portion of 30 to 60% by mass. It is preferable.
ゴム成分に対して配合する可塑剤としては、スピンドルオイル、アロマオイル、リキッドオイル、またはそれらの混合物等の従来の可塑剤、並びに脂肪酸金属塩が挙げられる。そして、ゴム成分100質量部に対して50〜210質量部の割合で配合される可塑剤のうち、1〜20質量部が脂肪酸金属塩であることが好ましく、11〜20質量部が脂肪酸金属塩であることが更に好ましい。 Examples of the plasticizer blended with the rubber component include conventional plasticizers such as spindle oil, aroma oil, liquid oil, or mixtures thereof, and fatty acid metal salts. And it is preferable that 1-20 mass parts is a fatty acid metal salt among the plasticizer mix | blended in the ratio of 50-210 mass parts with respect to 100 mass parts of rubber components, and 11-20 mass parts is fatty acid metal salt. More preferably.
ここで、脂肪酸金属塩には、飽和脂肪酸の金属塩、不飽和脂肪酸の金属塩、またはそれらの混合物を用いることができる。具体的には、脂肪酸金属塩としては、パルミチン酸、ステアリン酸、カプロン酸、カプリル酸、カプリン酸、ラウリン酸、ミリスチン酸、アラキジン酸、ベヘニン酸、セロチン酸、モンタン酸、メリシン酸等の飽和脂肪酸の金属塩、或いは、ゾーマリン酸、ペトロセリン酸、オレイン酸、エルシン酸、鯨油酸、リノール酸、エレオステアリン酸、モロクチ酸、バリナリン酸、イワシ酸、ヒラガシラ酸、ニシン酸、リシノレイン酸、ラウロレイン酸、エライジン酸、エルカ酸、リノエライジン酸、リノレン酸、アラキドン酸等の不飽和脂肪酸の金属塩が挙げられる。そして、上述した飽和脂肪酸または不飽和脂肪酸と金属塩を形成する金属元素としては、亜鉛等が挙げられる。 Here, as the fatty acid metal salt, a metal salt of a saturated fatty acid, a metal salt of an unsaturated fatty acid, or a mixture thereof can be used. Specifically, fatty acid metal salts include saturated fatty acids such as palmitic acid, stearic acid, caproic acid, caprylic acid, capric acid, lauric acid, myristic acid, arachidic acid, behenic acid, serotic acid, montanic acid, and melicic acid. Or metal salts of zomarinic acid, petroceric acid, oleic acid, erucic acid, whale oil acid, linoleic acid, eleostearic acid, moloctic acid, valinalic acid, sardine acid, hiragasiraic acid, nisinic acid, ricinoleic acid, lauroleic acid, Examples thereof include metal salts of unsaturated fatty acids such as elaidic acid, erucic acid, linoelaidic acid, linolenic acid and arachidonic acid. And as a metal element which forms a metal salt with the saturated fatty acid or unsaturated fatty acid mentioned above, zinc etc. are mentioned.
また、本発明のゴム組成物には、ゴム成分100質量部に対して、60〜200質量部のカーボンブラック、特にはSAF、ISAF、HAFグレードのカーボンブラックを補強性充填剤として配合しても良い。また、本発明のゴム組成物には、加硫剤、加硫促進剤、充填剤、老化防止剤等の通常用いられる配合剤を適宜配合しても良い。 Further, in the rubber composition of the present invention, 60 to 200 parts by mass of carbon black, particularly SAF, ISAF, and HAF grade carbon black may be blended as a reinforcing filler with respect to 100 parts by mass of the rubber component. good. Moreover, you may mix | blend normally used compounding agents, such as a vulcanizing agent, a vulcanization accelerator, a filler, an anti-aging agent, with the rubber composition of this invention suitably.
本発明のゴム組成物は、上記配合量で可塑剤をゴム成分に配合した以外特に制限はなく、例えば、以下のようにして製造することができる。 The rubber composition of the present invention is not particularly limited except that the plasticizer is blended with the rubber component in the above blending amount. For example, the rubber composition can be produced as follows.
上記脂肪酸金属塩を含む可塑剤を、任意の充填剤(カーボンブラック等)および添加剤とともにゴム成分に配合して混練する。なお、本発明のゴム組成物の調製方法に特に制限はなく、例えば、バンバリーミキサーやロール等を用いて、ゴム成分に、可塑剤と、必要に応じて適宜選択した各種配合剤とを練り込んで調製することができる。 The plasticizer containing the fatty acid metal salt is blended with a rubber component together with an optional filler (carbon black or the like) and an additive and kneaded. The method for preparing the rubber composition of the present invention is not particularly limited. For example, using a Banbury mixer, a roll or the like, a rubber component is kneaded with a plasticizer and various compounding agents appropriately selected as necessary. Can be prepared.
<タイヤ>
本発明のタイヤは、少なくとも一部を上記ゴム組成物で構成したことを特徴とし、それ以外は通常のタイヤと同様の製造方法を用いて製造することができる。
<Tire>
The tire of the present invention is characterized in that at least a part thereof is composed of the rubber composition, and other than that, it can be manufactured using the same manufacturing method as that of a normal tire.
次に、本発明のタイヤを、図を参照しながら詳細に説明する。図1は、本発明のタイヤの一例の断面図である。図1に示すタイヤは、一対のビード部1及び一対のサイドウォール部2と、両サイドウォール部2に連なるトレッド部3とを有し、上記一対のビード部1間にトロイド状に延在してこれら各部1,2,3を補強するカーカス4と、該カーカス4のクラウン部のタイヤ半径方向外側に位置するベルト5とを具える。 Next, the tire of the present invention will be described in detail with reference to the drawings. FIG. 1 is a cross-sectional view of an example of the tire of the present invention. The tire shown in FIG. 1 has a pair of bead portions 1, a pair of sidewall portions 2, and a tread portion 3 connected to both sidewall portions 2, and extends in a toroid shape between the pair of bead portions 1. The carcass 4 that reinforces the parts 1, 2, and 3 and the belt 5 that is located on the outer side in the tire radial direction of the crown portion of the carcass 4 are provided.
図示例のタイヤにおいて、カーカス4は、一枚のカーカスプライからなり、上記ビード部1内に夫々配設した一対のビードコア(ワイヤ)6間にトロイド状に延在する本体部と、各ビードコア6の周りでタイヤ幅方向の内側から外側に向けて半径方向外方に巻上げた折り返し部とからなる。なお、図示例のカーカス4は、一枚のカーカスプライよりなるが、本発明のタイヤにおいては、カーカスプライの枚数は複数であってもよい。 In the illustrated tire, the carcass 4 is composed of a single carcass ply, and a main body portion extending in a toroid shape between a pair of bead cores (wires) 6 disposed in the bead portion 1, and each bead core 6. And a folded portion wound up radially outward from the inner side to the outer side in the tire width direction. In the illustrated example, the carcass 4 is composed of one carcass ply. However, in the tire of the present invention, a plurality of carcass plies may be provided.
また、図示例のタイヤにおいて、ベルト5は、二枚のベルト層からなるが、本発明のタイヤにおいて、ベルトを構成するベルト層の枚数は一枚以上であればよく、これに限られるものではない。更に、本発明のタイヤは、ベルト5のタイヤ半径方向外側に、タイヤ周方向に対し実質的に平行に配列したコードのゴム引き層からなるベルト補強層を具えてもよく、ベルト5の端部と該ベルト補強層との間に更に層間ゴムを具えることもできる。 In the illustrated tire, the belt 5 is composed of two belt layers. However, in the tire of the present invention, the number of belt layers constituting the belt may be one or more, and is not limited thereto. Absent. Furthermore, the tire of the present invention may further include a belt reinforcing layer made of a rubberized layer of cords arranged substantially parallel to the tire circumferential direction on the outer side in the tire radial direction of the belt 5. Further, an interlayer rubber can be provided between the belt reinforcing layer and the belt reinforcing layer.
そして、図示例のタイヤは、少なくともトレッド部3に、上述したゴム組成物を用いることを特徴とする。 And the tire of the example of illustration uses the rubber composition mentioned above for the tread part 3 at least.
なお、本発明のタイヤに充填する気体としては、通常の或いは酸素分圧を調整した空気の他、窒素、アルゴン、ヘリウム等の不活性ガスを用いることができる。 In addition, as gas with which the tire of the present invention is filled, an inert gas such as nitrogen, argon, helium, etc. can be used in addition to air having normal or oxygen partial pressure adjusted.
以下に、実施例を挙げて本発明を更に詳しく説明するが、本発明は下記の実施例に何ら限定されるものではない。 Hereinafter, the present invention will be described in more detail with reference to examples. However, the present invention is not limited to the following examples.
(実施例1〜6)
表1に示す配合処方のゴム組成物を常法に従って作製した。そして、作製したゴム組成物をトレッドゴムとして使用した乗用車用タイヤ(サイズ:225/40 R18)を通常の方法で作製した。そして、作製したタイヤについて、下記の方法でグリップ性および耐摩耗性を測定・評価した。結果を表1に示す。
(Examples 1-6)
A rubber composition having a formulation shown in Table 1 was prepared according to a conventional method. And the tire (size: 225/40 R18) for passenger cars which used the produced rubber composition as a tread rubber was produced by the normal method. The produced tire was measured and evaluated for grip properties and wear resistance by the following methods. The results are shown in Table 1.
(実施例7〜12)
カーボンブラックおよびアロマオイルの配合量を変更した以外は実施例1〜6と同様にして、表2に示す配合処方のゴム組成物を作製した。そして、実施例1〜6と同様にして乗用車用タイヤを作製し、グリップ性および耐摩耗性を評価した。結果を表2に示す。
(Examples 7 to 12)
A rubber composition having the formulation shown in Table 2 was prepared in the same manner as in Examples 1 to 6 except that the blending amounts of carbon black and aroma oil were changed. And the tire for passenger cars was produced similarly to Examples 1-6, and grip property and abrasion resistance were evaluated. The results are shown in Table 2.
(実施例13〜18)
カーボンブラックおよびアロマオイルの配合量を変更した以外は実施例1〜6と同様にして、表3に示す配合処方のゴム組成物を作製した。そして、実施例1〜6と同様にして乗用車用タイヤを作製し、グリップ性および耐摩耗性を評価した。結果を表3に示す。
(Examples 13 to 18)
A rubber composition having the formulation shown in Table 3 was prepared in the same manner as in Examples 1 to 6 except that the blending amounts of carbon black and aroma oil were changed. And the tire for passenger cars was produced similarly to Examples 1-6, and grip property and abrasion resistance were evaluated. The results are shown in Table 3.
(比較例1〜12)
可塑剤として脂肪酸亜鉛塩を使用しなかった以外は実施例1〜18と同様にして、表1〜3に示す配合処方のゴム組成物を作製した。そして、実施例1〜18と同様にして乗用車用タイヤを作成し、グリップ性および耐摩耗性を評価した。結果を表1〜3に示す。
(Comparative Examples 1-12)
Except not using fatty acid zinc salt as a plasticizer, it carried out similarly to Examples 1-18, and produced the rubber composition of the mixing | blending prescription shown in Tables 1-3. And the tire for passenger cars was created like Examples 1-18, and grip property and abrasion resistance were evaluated. The results are shown in Tables 1-3.
(グリップ性)
最高時速300km/hで走行可能な高性能車両に作製したタイヤを装着し、当該高性能車両をサーキットで20周走行させてタイムを測定した。そして、計測した20Lapの平均タイムを算出し、結果を、実施例1〜6および比較例2〜4については比較例1を、実施例7〜12および比較例6〜8については比較例5を、実施例13〜18および比較例10〜12については比較例9を100として指標化して5段階評価した。プラス(+)の数値ほどタイムが早くタイヤのグリップ性が良いことを示す。
(Grip property)
The tires were mounted on a high-performance vehicle capable of traveling at a maximum speed of 300 km / h, and the high-performance vehicle was driven 20 laps on the circuit to measure time. And the average time of measured 20Lap is calculated, and the result is Comparative Example 1 for Examples 1 to 6 and Comparative Examples 2 to 4, and Comparative Example 5 for Examples 7 to 12 and Comparative Examples 6 to 8. In Examples 13 to 18 and Comparative Examples 10 to 12, Comparative Example 9 was indexed as 100 and evaluated in five stages. A positive (+) value means faster time and better tire grip.
(耐摩耗性)
最高時速300km/hで走行可能な高性能車両に作製したタイヤを装着し、当該高性能車両をサーキットで20周走行させた。そして、20Lap後のタイヤのトレッド部の残溝をデプスゲージで測定し、結果を、実施例1〜6および比較例2〜4については比較例1を、実施例7〜12および比較例6〜8については比較例5を、実施例13〜18および比較例10〜12については比較例9を100として指標化して摩耗深さを5段階評価した。プラス(+)の数値ほど摩耗が少なくタイヤの耐摩耗性が高いことを示す。
(Abrasion resistance)
The tire produced was mounted on a high performance vehicle capable of traveling at a maximum speed of 300 km / h, and the high performance vehicle was allowed to travel 20 laps on the circuit. And the remaining groove | channel of the tread part of the tire after 20 Lap was measured with the depth gauge, the result was compared with Example 1 about Examples 1-6 and Comparative Examples 2-4, Examples 7-12 and Comparative Examples 6-8. The comparative example 5 was indexed, and the comparative examples 9 to 100 were indexed as Comparative Example 5 and Comparative Examples 9 to 100 as 100, and the wear depth was evaluated in five stages. A positive (+) value indicates less wear and higher tire wear resistance.
1) スチレン−ブタジエンゴム(E−SBR、JSR株式会社製、1712):ゴム成分100質量部に対して37.5質量部のアロマオイルで油展、スチレンを23.5質量%含有
2) 東海カーボン株式会社製、シースト9H(窒素吸着比表面積(N2SA):142m2/g、ジブチルフタレート吸油量:130ml/100g)
3) 三共油化工業株式会社製、A/O MIX
4) 新日本石油株式会社製、スーパーオイルY22
5) SARTOMER社製、RICON100
6) SCHILL&SEILACHER社製、STRUKTOL VP1405
7) RHEIN CHEMIE社製、アクチブラストPP
8) 精工化学株式会社製、マイクロクリスタリンワックス
9) 大内新興化学工業株式会社製、N−(1,3−ジメチルブチル)−N’−フェニル−p−フェニレンジアミン
10) 三新化学工業株式会社製、ビス(4−メチルジベンゾチアゾリル−2)−ジスルフィド
1) Styrene-butadiene rubber (E-SBR, manufactured by JSR Corporation, 1712): Oil-extended with 37.5 parts by mass of aroma oil based on 100 parts by mass of rubber component, containing 23.5% by mass of styrene
2) Toast Carbon Co., Ltd., Seast 9H (nitrogen adsorption specific surface area (N 2 SA): 142 m 2 / g, dibutyl phthalate oil absorption: 130 ml / 100 g)
3) A / O MIX made by Sankyo Oil Chemical Co., Ltd.
4) Super Oil Y22 made by Nippon Oil Corporation
5) RICON100, manufactured by SARTOMER
6) STRILLTOL VP1405, manufactured by SCHILL & SEILACHER
7) Activ Blast PP, manufactured by RHEIN CHEMIE
8) Microcrystalline wax manufactured by Seiko Chemical Co., Ltd.
9) N- (1,3-dimethylbutyl) -N'-phenyl-p-phenylenediamine, manufactured by Ouchi Shinsei Chemical Co., Ltd.
10) Bis (4-methyldibenzothiazolyl-2) -disulfide, manufactured by Sanshin Chemical Industry Co., Ltd.
表1〜3の実施例1〜18および比較例1〜12より、従来の可塑剤(スピンドルオイル、リキッドオイル等)に代えて脂肪酸亜鉛塩を配合したゴム組成物をトレッドゴムとして用いることにより、グリップ性を向上させつつ耐摩耗性の低減を抑制したタイヤを提供できることが分かった。 From Examples 1 to 18 and Comparative Examples 1 to 12 in Tables 1 to 3, by using a rubber composition containing a fatty acid zinc salt instead of a conventional plasticizer (spindle oil, liquid oil, etc.) as a tread rubber, It has been found that it is possible to provide a tire that improves the grip and suppresses the reduction in wear resistance.
1 ビード部
2 サイドウォール部
3 トレッド部
4 カーカス
5 ベルト
6 ビードコア
1 Bead part 2 Side wall part 3 Tread part 4 Carcass 5 Belt 6 Bead core
Claims (6)
前記可塑剤のうち1〜20質量部が脂肪酸金属塩よりなることを特徴とする、ゴム組成物。 A rubber composition containing 50 to 210 parts by mass of a plasticizer with respect to 100 parts by mass of a rubber component,
1-20 mass parts among the said plasticizers consist of a fatty-acid metal salt, The rubber composition characterized by the above-mentioned.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2009098069A JP2010248338A (en) | 2009-04-14 | 2009-04-14 | Rubber composition and tire using the same |
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2009098069A JP2010248338A (en) | 2009-04-14 | 2009-04-14 | Rubber composition and tire using the same |
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| Publication Number | Publication Date |
|---|---|
| JP2010248338A true JP2010248338A (en) | 2010-11-04 |
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| Application Number | Title | Priority Date | Filing Date |
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| JP2009098069A Pending JP2010248338A (en) | 2009-04-14 | 2009-04-14 | Rubber composition and tire using the same |
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Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9670341B2 (en) | 2012-11-02 | 2017-06-06 | Bridgestone Corporation | Rubber compositions comprising metal carboxylates and processes for making the same |
| US10179479B2 (en) | 2015-05-19 | 2019-01-15 | Bridgestone Americas Tire Operations, Llc | Plant oil-containing rubber compositions, tread thereof and race tires containing the tread |
Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS59193938A (en) * | 1983-03-28 | 1984-11-02 | ユニロイヤル,インコ−ポレ−テツド | Elastomer composition |
| JP2001310987A (en) * | 2000-04-27 | 2001-11-06 | Kuraray Co Ltd | Thermoplastic polymer composition |
| JP2002020542A (en) * | 2000-07-07 | 2002-01-23 | Bridgestone Corp | Rubber composition and pneumatic tire using the composition |
| JP2005120335A (en) * | 2003-09-26 | 2005-05-12 | Sumitomo Chemical Co Ltd | Hollow sponge and automotive sealing material |
| JP2005220181A (en) * | 2004-02-04 | 2005-08-18 | Bridgestone Corp | Tire tread rubber composition and pneumatic tire using the same |
| JP2007039583A (en) * | 2005-08-04 | 2007-02-15 | Sumitomo Rubber Ind Ltd | Rubber composition for tire tread |
| JP2007161792A (en) * | 2005-12-12 | 2007-06-28 | Sumitomo Rubber Ind Ltd | Pneumatic tire having rubber composition and tire tread using the same |
-
2009
- 2009-04-14 JP JP2009098069A patent/JP2010248338A/en active Pending
Patent Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS59193938A (en) * | 1983-03-28 | 1984-11-02 | ユニロイヤル,インコ−ポレ−テツド | Elastomer composition |
| JP2001310987A (en) * | 2000-04-27 | 2001-11-06 | Kuraray Co Ltd | Thermoplastic polymer composition |
| JP2002020542A (en) * | 2000-07-07 | 2002-01-23 | Bridgestone Corp | Rubber composition and pneumatic tire using the composition |
| JP2005120335A (en) * | 2003-09-26 | 2005-05-12 | Sumitomo Chemical Co Ltd | Hollow sponge and automotive sealing material |
| JP2005220181A (en) * | 2004-02-04 | 2005-08-18 | Bridgestone Corp | Tire tread rubber composition and pneumatic tire using the same |
| JP2007039583A (en) * | 2005-08-04 | 2007-02-15 | Sumitomo Rubber Ind Ltd | Rubber composition for tire tread |
| JP2007161792A (en) * | 2005-12-12 | 2007-06-28 | Sumitomo Rubber Ind Ltd | Pneumatic tire having rubber composition and tire tread using the same |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9670341B2 (en) | 2012-11-02 | 2017-06-06 | Bridgestone Corporation | Rubber compositions comprising metal carboxylates and processes for making the same |
| US10179479B2 (en) | 2015-05-19 | 2019-01-15 | Bridgestone Americas Tire Operations, Llc | Plant oil-containing rubber compositions, tread thereof and race tires containing the tread |
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