Method for producing modified conjugated diene polymer/copolymer, modified conjugated diene polymer/copolymer, and rubber composition and tier using the same
一种橡胶组合物、共轭二烯的技术,应用在特殊轮胎、轮胎零部件、车轮等方向,能够解决滚动阻力性能恶化等问题
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preparation example Construction
[0261] In the case of adding the condensation accelerator during the preparation of the rubber composition I, it is preferable that the condensation accelerator and other components are usually at a temperature of about 20 to 185°C, preferably at a temperature of 60 to 175°C in the first stage. Mix down.
[0262] From the viewpoint of reactivity between silica and silanol, the content of the condensation accelerator in the rubber composition I is preferably 0.1 to 10 parts by mass, more preferably 0.5 to 5 parts by mass, based on 100 parts by mass of the rubber component.
[0263] The rubber component of the rubber composition I of the present invention is preferably composed of 10 to 100% by mass of the modified conjugated diene (co)polymer I represented by the above general formula (3) or the above general formula (4) and 90 to 0 % by mass of diene rubber. This is because the effect of the present invention can be enjoyed if the modified conjugated diene (co)polymer I is 10...
Embodiment
[0454] Next, the present invention will be described in further detail through examples, but the present invention is by no means limited by these examples.
[0455] In addition, the alcohol volatilization amount of the modified conjugated diene (co)polymer obtained in the following examples, the silanol production rate of the modified conjugated diene (co)polymer, and the dynamic loss tangent of the vulcanized rubber composition (tanδ) was measured according to the following method.
[0456] (1) Alcohol volatility
[0457] The sample was treated with a siloxane hydrolysis reagent composed of (0.2 mol / L toluenesulfonic acid) / (0.24 mol / L water) in a solvent containing 15% by mass of n-butanol and 85% by mass of toluene, and measured by headspace gas chromatography Stoichiometric amount of ethanol derived from [EtOSi] remaining in the tested modified conjugated diene (co)polymer.
[0458] (2) Silanol formation rate of modified conjugated diene (co)polymer
[0459]The amount o...
Synthetic example 1
[0470] Synthesis Example 1 (Synthesis of organosilane compound a used in the modification reaction step)
[0471] In a dry, nitrogen-substituted 300-ml pressure-resistant glass container, prepare 1 mol / liter of cyclohexane solution, dropwise add 2 mol / liter of diethyl ether solution of methyllithium (MeLi) with 2 times the molar amount, and stir fully to prepare organosilane compound a{N-(1,3-dimethyl Modifier solution (a) of butylene-3-(dimethylethoxysilyl)-1-propylamine}.
[0472] In addition, as N-(1,3-dimethylbutylene)-3-(triethoxysilyl)-1-propylamine, a product manufactured by Chisso Corporation under the trademark "Sila-Ace S340" was used.
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