Pneumatic tire
A technology of pneumatic tires and polymers, applied in special tires, tire parts, transportation and packaging, etc., can solve the problems of damaging the appearance of tires, and achieve the effect of improving the balance of ozone resistance and heat resistance
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment
[0139] The present invention is specifically described with reference to the following examples, but is not limited to the following examples.
[0140] The chemicals used in the synthesis or polymerization are shown below. Purify chemicals by conventional methods if necessary.
[0141] n-Hexane: product of Kanto Chemical Co., Ltd.
[0142] Styrene: product of Kanto Chemical Co., Ltd.
[0143] Butadiene: 1,3-butadiene purchased from Tokyo Chemical Industry Co., Ltd.
[0144] THF: Tetrahydrofuran purchased from Kanto Chemical Co., Ltd.
[0145] TMEDA: N,N,N',N'-Tetramethylethylenediamine available from Kanto Chemical Co., Ltd.
[0146] n-butyllithium solution: 1.6 M n-butyllithium solution in hexane purchased from Kanto Chemical Co., Ltd.
[0147] Ethanol: product of Kanto Chemical Co., Ltd.
[0148] 2,6-di-tert-butyl-p-cresol: Nocrac 200 purchased from Ouchi Shinko Chemical Industry Co., Ltd.
[0149] Amine modifier: N,N-bis(trimethylsilyl)-aminopropylmethyldiethoxysilan...
manufacture example
[0160] Synthesis Example 1 (synthetic polymer (1): SBR with a degree of hydrogenation of 0 mol %)
[0161] Add 2,000 mL of n-hexane, 60 g of styrene, 140 g of butadiene, 2.5 g of THF, and 0.45 mmol of n-butyl lithium into a heat-resistant reaction vessel that has been fully purged with nitrogen, and then stir at 50°C for 5 hours to Polymerization occurs. After the reaction was terminated by adding ethanol, 1 g of 2,6-di-tert-butyl-p-cresol was added to the reaction solution. The resulting solution was purified by reprecipitation to obtain polymer (1). Polymer (1) had a weight average molecular weight (Mw) of 490,000, and its styrene content was 30% by mass.
[0162] Synthesis Example 2 (synthetic polymer (2): hydrogenated SBR with a hydrogenation degree of 60 mol %)
[0163] Polymer (2) was produced as described in Synthesis of Polymer (1) except that the resulting polymer was subjected to hydrogenation. Specifically, after the polymerization conversion reaction in the syn...
PUM
| Property | Measurement | Unit |
|---|---|---|
| glass transition temperature | aaaaa | aaaaa |
| glass transition temperature | aaaaa | aaaaa |
| glass transition temperature | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
Login to View More 


