JP5731768B2 - Rubber composition and tire - Google Patents
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- JP5731768B2 JP5731768B2 JP2010180481A JP2010180481A JP5731768B2 JP 5731768 B2 JP5731768 B2 JP 5731768B2 JP 2010180481 A JP2010180481 A JP 2010180481A JP 2010180481 A JP2010180481 A JP 2010180481A JP 5731768 B2 JP5731768 B2 JP 5731768B2
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- 229920001971 elastomer Polymers 0.000 title claims description 104
- 239000005060 rubber Substances 0.000 title claims description 104
- 239000000203 mixture Substances 0.000 title claims description 61
- 239000003795 chemical substances by application Substances 0.000 claims description 24
- 239000002736 nonionic surfactant Substances 0.000 claims description 24
- 229920003048 styrene butadiene rubber Polymers 0.000 claims description 20
- 230000003712 anti-aging effect Effects 0.000 claims description 18
- 244000043261 Hevea brasiliensis Species 0.000 claims description 15
- 229920003052 natural elastomer Polymers 0.000 claims description 15
- 229920001194 natural rubber Polymers 0.000 claims description 15
- 150000001412 amines Chemical group 0.000 claims description 12
- 150000001875 compounds Chemical class 0.000 claims description 11
- 229920002857 polybutadiene Polymers 0.000 claims description 10
- 125000004432 carbon atom Chemical group C* 0.000 claims description 8
- 125000003342 alkenyl group Chemical group 0.000 claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 7
- 239000004094 surface-active agent Substances 0.000 claims description 7
- 150000001993 dienes Chemical class 0.000 claims description 6
- 229920003051 synthetic elastomer Polymers 0.000 claims description 6
- 239000005061 synthetic rubber Substances 0.000 claims description 6
- 125000002947 alkylene group Chemical group 0.000 claims description 5
- 229920003049 isoprene rubber Polymers 0.000 claims description 5
- 125000004122 cyclic group Chemical group 0.000 claims description 3
- 238000002845 discoloration Methods 0.000 description 24
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 19
- 239000001993 wax Substances 0.000 description 14
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 13
- 239000000377 silicon dioxide Substances 0.000 description 9
- 238000013329 compounding Methods 0.000 description 6
- 239000002174 Styrene-butadiene Substances 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- 238000000034 method Methods 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 238000004073 vulcanization Methods 0.000 description 4
- 229940126062 Compound A Drugs 0.000 description 3
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 3
- 239000006229 carbon black Substances 0.000 description 3
- 239000012763 reinforcing filler Substances 0.000 description 3
- 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 2
- 239000005062 Polybutadiene Substances 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 230000003078 antioxidant effect Effects 0.000 description 2
- 238000000149 argon plasma sintering Methods 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 230000002401 inhibitory effect Effects 0.000 description 2
- 229920000307 polymer substrate Polymers 0.000 description 2
- 230000003068 static effect Effects 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000004636 vulcanized rubber Substances 0.000 description 2
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
- 0 *C(C(C1O)O)OCC1O Chemical compound *C(C(C1O)O)OCC1O 0.000 description 1
- XZIIFPSPUDAGJM-UHFFFAOYSA-N 6-chloro-2-n,2-n-diethylpyrimidine-2,4-diamine Chemical compound CCN(CC)C1=NC(N)=CC(Cl)=N1 XZIIFPSPUDAGJM-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229920001213 Polysorbate 20 Polymers 0.000 description 1
- 229920001214 Polysorbate 60 Polymers 0.000 description 1
- 239000006087 Silane Coupling Agent Substances 0.000 description 1
- 239000004902 Softening Agent Substances 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 244000269722 Thea sinensis Species 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000008119 colloidal silica Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- ATYBNKYOXTWSBY-UHFFFAOYSA-N ethoxy-[3-(3-ethoxysilylpropyltetrasulfanyl)propyl]silane Chemical compound CCO[SiH2]CCCSSSSCCC[SiH2]OCC ATYBNKYOXTWSBY-UHFFFAOYSA-N 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- -1 fatty acid ester Chemical class 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 125000001165 hydrophobic group Chemical group 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 239000004200 microcrystalline wax Substances 0.000 description 1
- 235000019808 microcrystalline wax Nutrition 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
- 230000000704 physical effect Effects 0.000 description 1
- 229940051841 polyoxyethylene ether Drugs 0.000 description 1
- 229920000056 polyoxyethylene ether Polymers 0.000 description 1
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 1
- 235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 1
- 239000001818 polyoxyethylene sorbitan monostearate Substances 0.000 description 1
- 235000010989 polyoxyethylene sorbitan monostearate Nutrition 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- LVTJOONKWUXEFR-FZRMHRINSA-N protoneodioscin Natural products O(C[C@@H](CC[C@]1(O)[C@H](C)[C@@H]2[C@]3(C)[C@H]([C@H]4[C@@H]([C@]5(C)C(=CC4)C[C@@H](O[C@@H]4[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@@H](O)[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@H](CO)O4)CC5)CC3)C[C@@H]2O1)C)[C@H]1[C@H](O)[C@H](O)[C@H](O)[C@@H](CO)O1 LVTJOONKWUXEFR-FZRMHRINSA-N 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 229940035044 sorbitan monolaurate Drugs 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Landscapes
- Tires In General (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Description
本発明は、ゴム組成物及び該ゴム組成物を用いたタイヤに関し、タイヤ外皮ゴムの茶変を改善することが可能で、特にトレッドゴム用に好適に用いることができるゴム組成物及びこれ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 can improve browning of a tire outer rubber, and can be suitably used particularly for a tread rubber. Related to the tire.
一般に、天然ゴムやジエン系合成ゴムを原料としたゴム物品は、オゾンの存在下で劣化が進行し、表面に亀裂が生じる。この亀裂は、ゴム物品にかかる静的及び動的応力により進行し、その結果、ゴム物品が破壊に至ってしまう。 In general, a rubber article made from natural rubber or a diene synthetic rubber is deteriorated in the presence of ozone, and a crack occurs on the surface. This crack progresses due to static and dynamic stress applied to the rubber article, and as a result, the rubber article is broken.
上記オゾンによる亀裂の発生及び進行を抑制するために、ゴム物品には、老化防止剤として、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等のアミン系老化防止剤を配合したゴム組成物が適用されている。また、該ゴム組成物には、オゾンからの静的保護を目的として、ゴム物品の表面に保護膜を形成するためにワックスが配合されている。 In order to suppress the occurrence and progression of cracks due to ozone, the rubber article has an anti-aging agent such as N- (1,3-dimethylbutyl) -N′-phenyl-p-phenylenediamine as an anti-aging agent. A rubber composition containing an agent is applied. The rubber composition contains a wax for forming a protective film on the surface of the rubber article for the purpose of static protection from ozone.
しかしながら、上記アミン系老化防止剤及びワックスは、オゾン存在下での亀裂の発生及び進行の抑制に有効であるものの、ゴム成分等のポリマー基質を通って移動しやすく、短期間でゴム物品、特にタイヤの表面に移行し、倉庫保管中及び使用中に該ゴム物品を変色させる等して外観を悪化させる。ここで、ワックスが表面に移行すると該表面が白変し、上記アミン系老化防止剤が表面に移行すると該表面が茶変してしまう。 However, although the amine-based anti-aging agent and the wax are effective in suppressing the generation and progress of cracks in the presence of ozone, they are easy to move through a polymer substrate such as a rubber component, and in a short period, particularly rubber articles, It shifts to the surface of the tire and deteriorates the appearance by changing the color of the rubber article during storage and use. Here, when the wax moves to the surface, the surface turns white, and when the amine-based anti-aging agent moves to the surface, the surface turns brown.
これに対し、タイヤサイドウォール用ゴム組成物ではポリオキシエチレンエーテル型非イオン系界面活性剤やソルビタン型界面活性剤を配合して、アミン系老化防止剤及びワックスによる変色を防止する技術が開示されている（特許文献１、特許文献２）。しかしながら、これら技術では、トレッド用ゴム組成物に対しては、それら変色を十分に防止することはできなかった。 In contrast, a rubber composition for a tire sidewall is disclosed a technique for preventing discoloration due to an amine anti-aging agent and wax by blending a polyoxyethylene ether type nonionic surfactant or a sorbitan type surfactant. (Patent Document 1, Patent Document 2). However, these techniques cannot sufficiently prevent the discoloration of the tread rubber composition.
そこで、本発明の目的は、タイヤのサイドウォール部のみならず、トレッド部に用いても耐オゾン性を悪化させることなく、アミン系老化防止剤及びワックスによる変色を防止し、タイヤの外観を良好に保つことができるゴム組成物及び該ゴム組成物を用いたタイヤを提供することにある。 Therefore, the object of the present invention is to prevent discoloration due to an amine anti-aging agent and wax without deteriorating ozone resistance even when used not only in the sidewall portion of the tire but also in the tread portion, and has a good tire appearance. An object of the present invention is to provide a rubber composition that can be maintained at a high temperature and a tire using the rubber composition.
本発明者らは、上記目的を達成するために鋭意検討した結果、ゴム成分に特定構造の非イオン系界面活性剤を配合することにより、タイヤのトレッド部に用いても耐オゾン性を悪化させることなく、アミン系老化防止剤及びワックスによる変色を防止することができるゴム組成物が得られることを見出し、本発明を完成させるに至った。 As a result of intensive studies to achieve the above object, the present inventors have deteriorated ozone resistance even when used in a tread portion of a tire by blending a rubber component with a nonionic surfactant having a specific structure. The present inventors have found that a rubber composition capable of preventing discoloration due to an amine-based anti-aging agent and wax can be obtained, and the present invention has been completed.
すなわち、本発明は、
［１］ジエン系合成ゴム及び天然ゴムから選択される少なくとも一種のゴム成分に対し、下記式(I)で表される化合物及び下記式(II)で表される化合物から選択される少なくとも一種の非イオン系界面活性剤を配合してなることを特徴とするゴム組成物、
[1] At least one compound selected from a compound represented by the following formula (I) and a compound represented by the following formula (II) with respect to at least one rubber component selected from diene-based synthetic rubber and natural rubber: A rubber composition comprising a nonionic surfactant,
［２］ワックスを配合した上記［１］に記載のゴム組成物、
［３］老化防止剤を配合した上記［１］又は［２］に記載のゴム組成物、
［４］前記老化防止剤がアミン系老化防止剤である上記［３］に記載のゴム組成物、
［５］前記ゴム成分１００質量部に対し、前記非イオン系界面活性剤を０．１〜１０質量部配合した上記［１］〜［４］のいずれかに記載のゴム組成物、
［６］前記ゴム成分として天然ゴム、イソプレンゴム、スチレン-ブタジエン共重合体ゴム及びポリブタジエンゴムから選ばれる少なくとも１種を含む上記［１］〜［５］のいずれかに記載のゴム組成物、
［７］前記ゴム成分がスチレン-ブタジエン共重合体ゴム単独、スチレン-ブタジエン共重合体ゴム及びポリブタジエンゴム、天然ゴム及びスチレン-ブタジエン共重合体ゴム、又は天然ゴム及びポリブタジエンゴムである上記［１］〜［６］のいずれかに記載のゴム組成物、
［８］前記ゴム成分１００質量部のうちスチレン-ブタジエン共重合体ゴムを５０〜１００質量部含む上記［１］〜［７］のいずれかに記載のゴム組成物、
［９］上記［１］〜［８］のいずれかに記載のゴム組成物をタイヤ外皮に適用したタイヤ、及び
［１０］タイヤ外皮がトレッド部又はサイドウォール部であるである上記［９］に記載のタイヤ、
を提供するものである。
[2] The rubber composition according to the above [1], which contains a wax,
[3] The rubber composition according to the above [1] or [2], which contains an antioxidant.
[4] The rubber composition according to [3], wherein the anti-aging agent is an amine-based anti-aging agent,
[5] The rubber composition according to any one of [1] to [4], wherein 0.1 to 10 parts by mass of the nonionic surfactant is blended with respect to 100 parts by mass of the rubber component.
[6] The rubber composition according to any one of the above [1] to [5], comprising at least one selected from natural rubber, isoprene rubber, styrene-butadiene copolymer rubber and polybutadiene rubber as the rubber component.
[7] The above [1], wherein the rubber component is styrene-butadiene copolymer rubber alone, styrene-butadiene copolymer rubber and polybutadiene rubber, natural rubber and styrene-butadiene copolymer rubber, or natural rubber and polybutadiene rubber. To [6], the rubber composition according to any one of
[8] The rubber composition according to any one of [1] to [7], wherein 50 to 100 parts by mass of a styrene-butadiene copolymer rubber is included in 100 parts by mass of the rubber component.
[9] A tire in which the rubber composition according to any one of [1] to [8] is applied to a tire skin, and [10] The above [9], wherein the tire skin is a tread portion or a sidewall portion. Listed tires,
Is to provide.
本発明によれば、ゴム成分に特定構造の非イオン系界面活性剤を配合してなり、タイヤのサイドウォール部のみならず、トレッド部に用いても耐オゾン性を悪化させることなく、アミン系老化防止剤及びワックスによる変色を防止することができるゴム組成物及び該ゴム組成物を用いたタイヤを提供することができる。 According to the present invention, a non-ionic surfactant having a specific structure is blended with a rubber component, and the amine system does not deteriorate ozone resistance even when used in a tread portion as well as a sidewall portion of a tire. A rubber composition capable of preventing discoloration due to an anti-aging agent and wax, and a tire using the rubber composition can be provided.
以下に、本発明を詳細に説明する。
本発明のゴム組成物は、ジエン系合成ゴム及び天然ゴムから選択される少なくとも一種のゴム成分に、上記式（I）又は式（II）で表される非イオン系界面活性剤の少なくとも一種を配合してなることを特徴とする。
タイヤ外皮の茶変は、老化防止剤及びワックスがゴム成分等のポリマー基質を通ってタイヤ表面に移行し、タイヤの表面にワックスが析出して凹凸面を形成し光散乱が起こり、その凹凸面に付着した老化防止剤が酸化されて茶色の着色物色に変わることで、茶変色に見えるものである。
本発明のゴム組成物においては、上記式（I）又は式（II）で表される非イオン系界面活性剤が、表面に析出したワックスの凹凸面を平滑面化することにより、光散乱状態を改善して茶変を改良する。すなわち、該非イオン系界面活性剤は、疎水基Ｒ2の長さ、親水基（Ｒ1Ｏ）の長さ（ｌ，ｍ，ｎ）が調整されゴム組成物との相溶性がコントロールされて、該ゴム組成物と適度の非相溶性を有しているために、タイヤ表面に析出して上記機能を発揮するものである。
ここで、本発明のゴム組成物において、上記非イオン系界面活性剤の配合量は、上記ゴム成分１００質量部に対し０．１〜１０質量部であることが好ましく、０．５〜７質量部であることが更に好ましく、０．５〜５質量部であることが極めて好ましい。０．１質量部以上では、アミン系老化防止剤やワックスによる変色を防止することができ、１０質量部以下では、界面活性剤のブルームによる過度の光沢を抑制することができ、表面粘着性による作業性の低下を抑えることができる。
また、この界面活性剤を加えることによって耐オゾン性は低下しない。
The present invention is described in detail below.
The rubber composition of the present invention contains at least one nonionic surfactant represented by the above formula (I) or formula (II) in at least one rubber component selected from diene synthetic rubber and natural rubber. It is characterized by blending.
The browning of the tire hull is caused by the anti-aging agent and the wax passing through the polymer substrate such as a rubber component to the tire surface, and the wax deposits on the surface of the tire to form an uneven surface and light scattering occurs. The anti-aging agent attached to the surface is oxidized and changed to a brown color, which makes it look brown.
In the rubber composition of the present invention, the nonionic surfactant represented by the above formula (I) or formula (II) smoothes the uneven surface of the wax deposited on the surface, whereby a light scattering state. To improve the tea change. That is, in the nonionic surfactant, the length of the hydrophobic group R 2 and the length (l, m, n) of the hydrophilic group (R 1 O) are adjusted, and the compatibility with the rubber composition is controlled. Since it has moderate incompatibility with the rubber composition, it precipitates on the tire surface and exhibits the above functions.
Here, in the rubber composition of the present invention, the amount of the nonionic surfactant is preferably 0.1 to 10 parts by mass, and 0.5 to 7 parts by mass with respect to 100 parts by mass of the rubber component. Part is more preferable, and 0.5 to 5 parts by mass is extremely preferable. When the amount is 0.1 parts by mass or more, discoloration due to an amine-based anti-aging agent or wax can be prevented, and when the amount is 10 parts by mass or less, excessive gloss due to the bloom of the surfactant can be suppressed. A decrease in workability can be suppressed.
Moreover, ozone resistance does not fall by adding this surfactant.
本発明のゴム組成物に用いるゴム成分としては、ジエン系合成ゴム及び天然ゴムが挙げられ、該ジエン系合成ゴムとしては、イソプレンゴム(ＩＲ)、ポリブタジエンゴム(ＢＲ)、スチレン-ブタジエン共重合体ゴム(ＳＢＲ)等が挙げられ、これらゴム成分は、１種単独で用いても２種以上をブレンドして用いてもよい。すなわち、ゴム成分として、天然ゴム、イソプレンゴム、スチレン-ブタジエン共重合体ゴム及びポリブタジエンゴムから選ばれる少なくとも１種を含むことが好ましい。そして、ゴム成分がスチレン-ブタジエン共重合体ゴム単独、スチレン-ブタジエン共重合体ゴム及びポリブタジエンゴムの混合物、天然ゴム及びスチレン-ブタジエン共重合体ゴムの混合物、又は天然ゴム及びポリブタジエンゴムの混合物であることがさらに好ましい。
なお、通常、トレッド部に好ましく用いられるゴム成分はＳＢＲが５０〜１００質量％とＳＢＲ主体であり、サイドウォール部に好ましく用いられるゴム成分は、天然ゴムとＢＲの混合物である。
Examples of the rubber component used in the rubber composition of the present invention include diene-based synthetic rubber and natural rubber. Examples of the diene-based synthetic rubber include isoprene rubber (IR), polybutadiene rubber (BR), and styrene-butadiene copolymer. Examples thereof include rubber (SBR). These rubber components may be used alone or in a blend of two or more. That is, the rubber component preferably contains at least one selected from natural rubber, isoprene rubber, styrene-butadiene copolymer rubber and polybutadiene rubber. The rubber component is a styrene-butadiene copolymer rubber alone, a mixture of styrene-butadiene copolymer rubber and polybutadiene rubber, a mixture of natural rubber and styrene-butadiene copolymer rubber, or a mixture of natural rubber and polybutadiene rubber. More preferably.
In general, the rubber component preferably used for the tread portion is SBR mainly having an SBR of 50 to 100% by mass, and the rubber component preferably used for the sidewall portion is a mixture of natural rubber and BR.
本発明のゴム組成物に用いる非イオン系界面活性剤は、上記式（I）又は式（II）で表される。該非イオン系界面活性剤は、１種単独で使用してもよいし、２種以上を併用してもよく、市販品を好適に使用することができる。 The nonionic surfactant used in the rubber composition of the present invention is represented by the above formula (I) or formula (II). This nonionic surfactant may be used individually by 1 type, may use 2 or more types together, and can use a commercial item suitably.
式（I）及び式（II）のＲ2は、それぞれ炭素数１〜１４のアルキル基又はアルケニル基を表し、該アルキル基及びアルケニル基は直鎖状、分枝鎖状及び環状の何れでもよい。これらアルキル基及びアルケニル基の炭素数は、主に変色度の観点から、１〜１４、好ましくは８〜１４、更に好ましくは１０〜１４である。 R 2 in formula (I) and formula (II) represents an alkyl group or alkenyl group having 1 to 14 carbon atoms, and the alkyl group and alkenyl group may be linear, branched or cyclic. . The carbon number of these alkyl groups and alkenyl groups is 1 to 14, preferably 8 to 14, and more preferably 10 to 14 mainly from the viewpoint of discoloration.
式（I）及び式（II）のＲ1は、炭素数２〜４のアルキレン基であり、好ましくは炭素数２又は３のアルキレン基であり、更に好ましくは炭素数２のアルキレン基である。
式（I）及び式（II）のｌ、ｍ及びｎは、変色度の観点から、それぞれ独立して好ましくは０〜５０であり、より好ましくは０〜３０、更に好ましくは０〜２０である。ｌ、ｍ、ｎの総和は、変色度の観点から、３〜５０であり、好ましくは４〜３０、より好ましくは６〜２０である。これらの観点から、ｌ、ｍ、ｎはそれぞれ独立して０〜５０で、かつｌ、ｍ、ｎの総和は３〜５０が好ましく、ｌ、ｍ、ｎはそれぞれ独立して０〜３０で、かつｌ、ｍ、ｎの総和は４〜３０がより好ましく、ｌ、ｍ、ｎはそれぞれ独立して０〜２０で、かつｌ、ｍ、ｎの総和は６〜２０が更に好ましい。
R 1 in formula (I) and formula (II) is an alkylene group having 2 to 4 carbon atoms, preferably an alkylene group having 2 or 3 carbon atoms, and more preferably an alkylene group having 2 carbon atoms.
In the formula (I) and the formula (II), l, m and n are each independently preferably 0 to 50, more preferably 0 to 30, further preferably 0 to 20 from the viewpoint of the degree of discoloration. . The total of l, m, and n is 3 to 50, preferably 4 to 30, and more preferably 6 to 20 from the viewpoint of the degree of color change. From these viewpoints, l, m and n are each independently 0 to 50, and the sum of l, m and n is preferably 3 to 50, and l, m and n are each independently 0 to 30; The total sum of l, m and n is more preferably 4 to 30, and l, m and n are each independently 0 to 20, and the sum of l, m and n is further preferably 6 to 20.
上記非イオン系界面活性剤は、ＨＬＢ値（親水性と親油性のバランス値）が８〜１９であるのが好ましい。ここで、本発明において、ＨＬＢ値は、下記に示すアトラス法による式で定義される。
ＨＬＢ＝２０（１−Ｓ／Ａ）
（式中、Ｓはエステル系界面活性剤の鹸化価であり、Ａは該界面活性剤を構成する脂肪酸の酸価である。）
The nonionic surfactant preferably has an HLB value (balance between hydrophilicity and lipophilicity) of 8 to 19. Here, in the present invention, the HLB value is defined by an expression based on the Atlas method shown below.
HLB = 20 (1-S / A)
(In the formula, S is the saponification value of the ester surfactant, and A is the acid value of the fatty acid constituting the surfactant.)
上記非イオン系界面活性剤のＨＬＢ値が８以上では親油性が抑制され、ゴムとの相溶性を抑えて、表面に移行させることができ、１９以下では、ゴムとの相溶性を高めて、混練を容易にし、かつ充填剤への吸着を抑制し、表面に移行させることができる。
上記非イオン系界面活性剤のＨＬＢ値は、１０〜１７であるのが更に好ましく、１１〜１７がより更に好ましい。ＨＬＢ値が１０以上では、表面への移行速度を高めて、茶変防止効果を促進することができ、１７以下では、ゴム組成物のスコーチタイムを短縮させることなく、作業性を低下させない。
When the HLB value of the nonionic surfactant is 8 or more, the lipophilicity is suppressed, and the compatibility with rubber can be suppressed and transferred to the surface, and when it is 19 or less, the compatibility with rubber is increased. Kneading can be facilitated, adsorption to the filler can be suppressed, and transfer to the surface can be achieved.
The HLB value of the nonionic surfactant is more preferably 10-17, and still more preferably 11-17. If the HLB value is 10 or more, the transition speed to the surface can be increased to promote the effect of preventing browning, and if it is 17 or less, the scorch time of the rubber composition is not shortened and workability is not lowered.
上記ゴム組成物には、オゾンによる亀裂の発生及び進行を抑制するために、アミン系老化防止剤及びワックスを配合するのが好ましい。ここで、アミン系老化防止剤としては、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等が挙げられる。 In order to suppress the occurrence and progress of cracks due to ozone, the rubber composition preferably contains an amine anti-aging agent and a wax. Here, examples of the amine-based antioxidant include N- (1,3-dimethylbutyl) -N′-phenyl-p-phenylenediamine.
また、上記ゴム組成物には、補強用充填剤として、カーボンブラックやシリカを含有させることができる。カーボンブラックとしては特に制限はなく、シリカも市販のあらゆるものを使用でき、なかでも湿式シリカ、乾式シリカ、コロイダルシリカを用いることが好ましく、湿式シリカを用いるのが特に好ましい。カーボンブラックやシリカは併用して用いてもよく、これら補強用充填剤の配合量は上記ゴム成分１００質量部に対し３０〜１２０質量部であることが好ましい。なお、補強用充填剤としてシリカを用いる場合は、補強性の観点から、シランカップリング剤をシリカ１００質量部に対して１〜２０質量部程度含有させることができ、発熱性の観点から５〜１５質量部の範囲で用いるのが好ましい。 The rubber composition may contain carbon black or silica as a reinforcing filler. Carbon black is not particularly limited, and any commercially available silica can be used. Among these, wet silica, dry silica, and colloidal silica are preferably used, and wet silica is particularly preferably used. Carbon black and silica may be used in combination, and the amount of these reinforcing fillers is preferably 30 to 120 parts by mass with respect to 100 parts by mass of the rubber component. When silica is used as the reinforcing filler, from the viewpoint of reinforcement, the silane coupling agent can be contained in an amount of about 1 to 20 parts by mass with respect to 100 parts by mass of silica. It is preferable to use in the range of 15 parts by mass.
該ゴム組成物には、更に、加硫剤、加硫促進剤、スコーチ防止剤、軟化剤、酸化亜鉛、ステアリン酸等のゴム業界で通常使用される配合剤を、本発明の目的を害しない範囲内で適宜選択し配合することができる。これら配合剤は、市販品を好適に使用することができる。 The rubber composition further contains a compounding agent usually used in the rubber industry such as a vulcanizing agent, a vulcanization accelerator, a scorch preventing agent, a softening agent, zinc oxide and stearic acid, which does not impair the purpose of the present invention. It can select suitably and mix | blend within the range. As these compounding agents, commercially available products can be suitably used.
なお、上記ゴム組成物は、ゴム成分と、非イオン系界面活性剤と、必要に応じて適宜選択した各種配合剤とを混練り、熱入れ、押出等することにより製造することができる。 In addition, the said rubber composition can be manufactured by knead | mixing a rubber component, a nonionic surfactant, and the various compounding agents suitably selected as needed, heat-inserting, extrusion, etc.
本発明の空気入りタイヤは、上記ゴム組成物をタイヤのゴム部材の何れかに適用したことを特徴とし、タイヤ外皮、特にトレッド部やサイドウォール部に適用したものが好ましい。かかるタイヤは、上記非イオン系界面活性剤を配合しているために、アミン系老化防止剤やワックスがタイヤ表面に移行して変色するのが防止されており、外観が長期に亘って良好である。 The pneumatic tire of the present invention is characterized in that the above rubber composition is applied to any of the rubber members of the tire, and is preferably applied to a tire outer skin, particularly a tread portion or a sidewall portion. Since the tire contains the nonionic surfactant, the amine anti-aging agent and the wax are prevented from being transferred to the tire surface and discolored, and the appearance is good for a long time. is there.
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１〜７及び比較例１〜７
表１に示す配合処方（ゴム成分としてＳＢＲ主体）でかつ表２に示す配合量の非イオン系界面活性剤を配合したゴム組成物を調製し、１６０℃で１４分間加硫した。得られた加硫ゴムに対し、下記の方法で引張応力、耐オゾン性、変色度を測定、評価した。その結果を表２に示す。
Examples 1-7 and Comparative Examples 1-7
A rubber composition containing the compounding formulation shown in Table 1 (mainly SBR as the rubber component) and the nonionic surfactant in the compounding amount shown in Table 2 was prepared and vulcanized at 160 ° C. for 14 minutes. The obtained vulcanized rubber was measured and evaluated for tensile stress, ozone resistance and discoloration by the following methods. The results are shown in Table 2.
（１）引張応力
ゴム物性の代表的指標として３００％伸長時の引張応力を測定した。具体的には、ＪＩＳ ３号ダンベル型試験片を用い、ＪＩＳ Ｋ ６２５１：２００４に従って３００％伸長時の引張応力を測定し、比較例１を１００として指数表示した。指数値が大きい程、３００％伸長時の引張応力が大きいことを示す。
(1) Tensile stress Tensile stress at 300% elongation was measured as a representative index of rubber physical properties. Specifically, the tensile stress at 300% elongation was measured according to JIS K 6251: 2004 using a JIS No. 3 dumbbell-type test piece, and the comparative example 1 was indicated as 100. A larger index value indicates a greater tensile stress at 300% elongation.
（２）耐オゾン性
ＪＩＳ Ｋ ６２５９：２００４に従い、温度４０℃、オゾン濃度５０ｐｐｈｍ、伸び２０％の条件にして、実施例１〜６及び比較例１〜６の作成した試験片についてオゾン劣化試験を行ない、５０時間後に試験片の劣化状態を観察し、クラック発生の有無で評価した。
(2) Ozone resistance According to JIS K 6259: 2004, the ozone deterioration test was performed on the test pieces prepared in Examples 1 to 6 and Comparative Examples 1 to 6 under the conditions of a temperature of 40 ° C., an ozone concentration of 50 pphm, and an elongation of 20%. After 50 hours, the test piece was observed for deterioration and evaluated for the presence or absence of cracks.
（３）変色度
色度計（「日本電色工業(株）、機種名ＮＦ３３３」）を用いて、顆粒ゴム試験片の変色度を評価した。測色したデータはＬ*、ａ*、ｂ*で表わした。Ｌ*値は明度、ａ*、ｂ*は色味を示している。ａ*値とｂ*値は０で無色、ａ*値が正であるほど赤、負であるほど緑、ｂ*値が正であるほど黄、負であるほど青であることを示す。変色度については、加硫直後のｂ*値、目視による加硫直後の変色の度合いにより、加硫直後の変色度を評価し、夏季の屋外放置（雨は当たらない屋根の下１日のうち特定の時間のみ直射日光が当たる）の環境条件下に、加硫ゴム片を１ヶ月放置した後のｂ*値及び目視による変色の度合いにより放置後の変色度を評価した。
変色度は５段階評価を行い、変色がひどく認められる場合を５とし、全体の半分以上に変色が認められる場合を４とし、全体の半分以下に変色が認められる場合を３とし、わずかに変色が認められる場合を２とし、変色が認められない場合を１とした。
(3) Discoloration degree Using a chromaticity meter ("Nippon Denshoku Industries Co., Ltd., model name NF333"), the discoloration degree of the granular rubber test piece was evaluated. The colorimetric data was represented by L *, a *, b *. L * value indicates lightness, and a * and b * indicate color. The a * value and the b * value are 0 and colorless, and the positive value of the a * value is red, the negative value is green, the positive b * value is yellow, and the negative value is blue. Regarding the degree of color change, the b * value immediately after vulcanization and the degree of color change immediately after vulcanization were evaluated based on the degree of color change immediately after vulcanization. The degree of discoloration after being allowed to stand was evaluated based on the b * value after leaving the vulcanized rubber piece for 1 month and the degree of discoloration by visual observation under the environmental conditions of direct sunlight only for a specific time).
The degree of discoloration is evaluated on a five-point scale, where 5 is the case where discoloration is severely recognized, 4 is the case where discoloration is observed in more than half of the whole, and 3 is the case where discoloration is observed in less than half of the whole. Is 2 and 1 is the case where no discoloration is observed.
また、化合物Ａをタイヤトレッド用ゴム組成物に配合したものと界面活性剤無配合のものとから、それぞれタイヤサイズ２０５／６５Ｒ１５の乗用車用ラジアルタイヤを定法によって作製し、上記と同様の変色試験を行った。その結果を表３に示す。 Further, radial tires for passenger cars with tire sizes 205 / 65R15 were prepared by a conventional method from those in which Compound A was blended with a rubber composition for tire treads and those without surfactants, respectively, and a discoloration test similar to the above was conducted. went. The results are shown in Table 3.
*１ ＪＳＲ(株）製「ＳＢＲ＃１５００」
*２ 東海カーボン(株）製「シースト７ＨＭ」
*３ 東ソーシリカ(株）製「ニプシールＡＱ」
*４ ビス（３−エトキシシリルプロピル）テトラスルフィド
*５ マイクロクリスタリンワックス，日本精蝋社製「オゾエース−０７０１」
*６ 大内新興化学工業(株）製「ノクラック６Ｃ」
*７ 精工化学社製「ノンフレックスＲＤ−Ｓ」
*８ 大内新興化学工業(株）製「ノクセラーＤ」
*９ 大内新興化学工業(株）製「ノクセラーＤＭ」
*１０ 三新化学工業社製「サンセラーＣＭ−Ｇ」
* 1 "SBR # 1500" manufactured by JSR Corporation
* 2 “Seast 7HM” manufactured by Tokai Carbon Co., Ltd.
* 3 “Nipseal AQ” manufactured by Tosoh Silica Corporation
* 4 Bis (3-ethoxysilylpropyl) tetrasulfide
* 5 Microcrystalline wax, Nippon Seiwa Co., Ltd. “Ozoace-0701”
* 6 “NOCRACK 6C” manufactured by Ouchi Shinsei Chemical Co., Ltd.
* 7 “Nonflex RD-S” manufactured by Seiko Chemical Co., Ltd.
* 8 “Noxeller D” manufactured by Ouchi Shinsei Chemical Co., Ltd.
* 9 “Noxeller DM” manufactured by Ouchi Shinsei Chemical Industry Co., Ltd.
* 10 "Sunseller CM-G" manufactured by Sanshin Chemical Industry Co., Ltd.
なお、表２において、化合物Ａは、花王(株）製非イオン系界面活性剤、商標「レオドールＴＷ-Ｌ１２０」（ポリオキシエチレンソルビタンモノヤシ油脂肪酸エステル）で、上記式(I)において、Ｒ2が主としてＣ11Ｈ23で、Ｒ1がＣ2Ｈ4、ｌ＋ｍ＋ｎが２０で、ＨＬＢ値が１６．７である化合物と、上記式(II)において、Ｒ2が主としてＣ11Ｈ23で、Ｒ1がＣ2Ｈ4、ｌ＋ｍ＋ｎが２０で、ＨＬＢ値が１６．７である化合物との混合物であり；
化合物Ｂは、花王(株）製非イオン系界面活性剤、商標「レオドールＴＷ-Ｌ１０６」（ポリオキシエチレンソルビタンモノラウレート）で、上記式(I)において、Ｒ2がＣ11Ｈ23で、Ｒ1がＣ2Ｈ4、ｌ＋ｍ＋ｎが４で、ＨＬＢ値が１３．３である化合物と、上記式(II)において、Ｒ2がＣ11Ｈ23で、Ｒ1がＣ2Ｈ4、ｌ＋ｍ＋ｎが６で、ＨＬＢ値が１３．３である化合物との混合物であり；
化合物Ｃは、花王(株）製非イオン系界面活性剤、商標「レオドールＳＰ-Ｌ１０」（ソルビタンモノラウレート）で、上記式(I)において、Ｒ2がＣ11Ｈ23で、Ｒ1がＣ2Ｈ4、ｌ，ｍ，ｎが０で、ＨＬＢ値が８．６である化合物と、上記式(II)において、Ｒ2がＣ11Ｈ23で、Ｒ1がＣ2Ｈ4、ｌ，ｍ，ｎが０で、ＨＬＢ値が８．６である化合物との混合物であり；
化合物Ｄは、花王(株）製非イオン系界面活性剤、商標「レオドールＴＷ−Ｓ１０６Ｖ」（ポリオキシエチレンソルビタンモノステアレート）で、上記式(I)において、Ｒ2がＣ17Ｈ35で、Ｒ1がＣ2Ｈ4、ｌ＋ｍ＋ｎが６で、ＨＬＢ値が９．６である化合物と、上記式(II)において、Ｒ2がＣ17Ｈ35で、Ｒ1がＣ2Ｈ4、ｌ＋ｍ＋ｎが６で、ＨＬＢ値が９．６である化合物との混合物である。
In Table 2, compound A is a nonionic surfactant manufactured by Kao Corporation, trademark “Leodol TW-L120” (polyoxyethylene sorbitan monococonut oil fatty acid ester), and in the above formula (I), R 2 is mainly C 11 H 23 , R 1 is C 2 H 4 , l + m + n is 20, and the HLB value is 16.7, and in the above formula (II), R 2 is mainly C 11 H 23 , A mixture with a compound wherein R 1 is C 2 H 4 , l + m + n is 20, and the HLB value is 16.7;
Compound B is a nonionic surfactant manufactured by Kao Corporation, trade name “Leodol TW-L106” (polyoxyethylene sorbitan monolaurate), and in the above formula (I), R 2 is C 11 H 23 , R 1 is C 2 H 4 , l + m + n is 4 and the HLB value is 13.3, and in the above formula (II), R 2 is C 11 H 23 , R 1 is C 2 H 4 , and l + m + n is 6 is a mixture with a compound having an HLB value of 13.3;
Compound C is a nonionic surfactant manufactured by Kao Corporation, trademark “Leodol SP-L10” (sorbitan monolaurate), and in the above formula (I), R 2 is C 11 H 23 , and R 1 is C 2 H 4 , l, m, n is 0 and the HLB value is 8.6, and in the above formula (II), R 2 is C 11 H 23 , R 1 is C 2 H 4 , l , M, n are 0, and a mixture with a compound having an HLB value of 8.6;
Compound D is a nonionic surfactant manufactured by Kao Corporation, trademark “Leodol TW-S106V” (polyoxyethylene sorbitan monostearate), wherein R 2 is C 17 H 35 in the above formula (I), R 1 is C 2 H 4 , l + m + n is 6 and the HLB value is 9.6, and in the above formula (II), R 2 is C 17 H 35 , R 1 is C 2 H 4 , and l + m + n is 6 is a mixture with a compound having an HLB value of 9.6.
表２から、実施例１〜６のゴム組成物は、１ヶ月の屋外放置試験後の変色度が良好であったのに対し、非イオン系界面活性剤を配合しない比較例１〜３のゴム組成物、ｌ，ｍ，ｎが０あるいはＲ2が大きく本発明の範囲外の非イオン系界面活性剤を配合した比較例４〜６のゴム組成物は屋外放置試験後の変色度が著しく悪いことがわかる。 From Table 2, the rubber compositions of Examples 1 to 6 had good discoloration after an outdoor standing test for one month, whereas the rubbers of Comparative Examples 1 to 3 not containing a nonionic surfactant The rubber compositions of Comparative Examples 4 to 6, in which l, m, n are 0 or R 2 is large and a nonionic surfactant outside the scope of the present invention is blended, the discoloration after the outdoor standing test is extremely poor. I understand that.
また、変色抑制効果の高い化合物Ａをタイヤトレッド用ゴム組成物に配合して乗用車用ラジアルタイヤを作製し、変色試験を行ったところ、表３に示すように、タイヤでも高い変色抑制効果があることがわかった。 Further, when a radial tire for a passenger car was prepared by compounding Compound A having a high discoloration inhibiting effect in a rubber composition for a tire tread and subjected to a discoloration test, as shown in Table 3, the tire also has a high discoloration inhibiting effect. I understood it.
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| EP11816489.6A EP2604650B1 (en) | 2010-08-11 | 2011-08-11 | Rubber composition, method for preventing discoloration of rubber composition, and tire |
| PCT/JP2011/068381 WO2012020826A1 (en) | 2010-08-11 | 2011-08-11 | Rubber composition, method for preventing discoloration of rubber composition, and tire |
| US13/816,145 US9200141B2 (en) | 2010-08-11 | 2011-08-11 | Rubber composition, method for preventing discoloration of rubber composition, and tire |
| CN201180039244.5A CN103097449B (en) | 2010-08-11 | 2011-08-11 | Rubber combination, rubber combination prevent color changing method and tire |
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| JP5960732B2 (en) * | 2013-07-05 | 2016-08-02 | 住友ゴム工業株式会社 | Rubber composition for tire and pneumatic tire |
| JP6151992B2 (en) * | 2013-07-05 | 2017-06-21 | 住友ゴム工業株式会社 | Pneumatic tire |
| JP6151991B2 (en) * | 2013-07-05 | 2017-06-21 | 住友ゴム工業株式会社 | Rubber composition for tire and pneumatic tire |
| WO2015145843A1 (en) * | 2014-03-26 | 2015-10-01 | 住友ゴム工業株式会社 | Rubber composition for tire, pneumatic tire, and method for manufacturing rubber composition for tire |
| CN108137856B (en) | 2015-10-02 | 2021-05-04 | 科慕埃弗西有限公司 | Solid polymeric article having hydrophobic compound intermixed therein |
| US11359099B2 (en) | 2015-10-02 | 2022-06-14 | The Chemours Company Fc, Llc | Hydrophobic extenders in fluorinated surface effect coatings |
| JP7009868B2 (en) * | 2017-01-31 | 2022-01-26 | 横浜ゴム株式会社 | Rubber Compositions for Studless Tires and Studless Tires |
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| JP4562384B2 (en) * | 2003-03-26 | 2010-10-13 | 株式会社ブリヂストン | Rubber composition and pneumatic tire using the same |
| JP4480529B2 (en) * | 2004-09-15 | 2010-06-16 | 株式会社ブリヂストン | Rubber composition and tire using the same |
| JP5234891B2 (en) * | 2007-05-01 | 2013-07-10 | 株式会社ブリヂストン | Rubber composition |
| JP5364315B2 (en) * | 2008-08-28 | 2013-12-11 | 株式会社ブリヂストン | Rubber composition and pneumatic tire |
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