Method for producing modified conjugated diene polymer, modified conjugated diene polymer, and rubber composition
一种橡胶组合物、共轭二烯的技术,应用在轮胎零部件、车辆部件、特殊轮胎等方向,能够解决改性改良少、橡胶组合物改性效果未必充分、无法获得橡胶改性效果等问题,达到加工性良好、耐磨耗性优异的效果
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Embodiment 1
[0176] Embodiment 1 (manufacture of modified polymer A):
[0177] In a nitrogen-substituted 5-liter reactor, 2.4 kg of cyclohexane and 300 g of 1,3-butadiene were charged under a nitrogen atmosphere. To this, a cyclohexane solution of neodymium tertiary carbonate (0.09 mmol), a toluene solution of methylaluminoxane (hereinafter also referred to as "MAO") (3.6 mmol), hydrogenated diisobutyl A toluene solution of aluminum (hereinafter also referred to as "DIBAH") (5.5mmol) and diethylaluminum chloride (0.18mmol) was reacted with 1,3-butadiene (4.5mmol) at 40°C and aged for 30 minutes. The obtained catalyst was polymerized at 60°C for 60 minutes. The reaction conversion of 1,3-butadiene was almost 100%.
[0178] Take out 200 g of this polymer solution into a methanol solution containing 0.2 g of 2,4-di-tert-butyl-p-cresol, stop the polymerization, remove the solvent by stripping, and dry with a roller at 110° C. to obtain Polymer before modification (conjugated diene polymer)....
Embodiment 2
[0184] Embodiment 2 (manufacture of modified polymer B):
[0185] In addition to using polymethylene polyphenyl polycyanate (trade name "PAPI*135" (manufactured by DOWCHEMICAL, Japan)) (hereinafter also referred to as "CMDI" (4.16mmol in NCO conversion)) instead of in Example 1 Modified polymer B (modified conjugated diene polymer) was obtained in the same manner as in Example 1, except for the PMDI (2.08 mmol). Table 1 shows the modification conditions and the results of the modification reaction.
Embodiment 3
[0186] Embodiment 3 (manufacture of modified polymer C):
[0187] Except using hexamethyldisilazane (hereinafter also referred to as "HMDS") instead of HMDA in Example 2, all the other operations were performed in the same manner as in Example 2 to obtain modified polymer C (modified conjugated di ethylenic polymers). Table 1 shows the modification conditions and the results of the modification reaction.
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