Active material for negative electrodes of nonaqueous secondary batteries, and nonaqueous secondary battery
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synthesis example 1
Preparation Example of Composite Resin (A)
[0116]Into a reaction container equipped with a stirrer, a thermometer, a dripping funnel, a cooling tube, and a nitrogen gas inlet, 191 g of phenyltrimethoxysilane (PTMS) was charged, and the temperature was increased to 120° C. Next, a mixture of 169 g of methyl methacrylate (MMA), 11 g of 3-methacryloyloxy propyltrimethoxysilane (MPTS), and 18 g of tert-butyl peroxy-2-ethylhexanoate (TBPEH) was dripped to the reaction container described above over 4 hours. Subsequently, stirring was performed for 16 hours at the same temperature as described above, so that a vinyl polymer (a2-1-1) having a trimethoxysilyl group was prepared.
[0117]Next, the temperature of the above reaction container was controlled at 80° C., 131 g of methyltrimethoxysilane (MTMS), 226 g of 3-acryloyloxy propyltrimethoxysilane (APTS), and 116 g of dimethyldimethoxysilane (DMDMS) were added to the above reaction container.
[0118]Subsequently, a mixture of 6.3 g of “A-3” [ma...
synthesis example 2
[0119]Into a reaction container similar to that in Synthesis Example 1-1, 250 g of PTMS was charged, and the temperature was increased to 120° C. Next, a mixture of 169 g of MMA, 11 g of MPTS, and 18 g of TBPEH was dripped to the reaction container described above over 4 hours. Subsequently, stirring was performed for 16 hours at the same temperature as described above, so that a vinyl polymer (a2-1-2) having a trimethoxysilyl group was prepared.
[0120]Next, the temperature of the above reaction container was controlled at 80° C., 172 g of MTMS, 113 g of APTS, and 151 g of DMDMS were added to the above reaction container. Subsequently, a mixture of 6.9 g of “A-3” and 105 g of deionized water was dripped for 5 minutes, and stirring was performed for 2 hours at the same temperature as described above to perform a hydrolysis condensation reaction, so that a reaction product was obtained. By the analysis of the reaction product using 1H-NMR, it was found that approximately 100% of the tr...
synthesis example 3
[0121]Into a reaction container similar to that in Synthesis Example 1-1, 164 g of PTMS was charged, and the temperature was increased to 120° C. Next, a mixture of 226 g of MMA, 14 g of MPTS, and 24 g of TBPEH was dripped to the reaction container described above over 4 hours. Subsequently, stirring was performed for 16 hours at the same temperature as described above, so that a vinyl polymer (a2-1-3) having a trimethoxysilyl group was prepared.
[0122]Next, the temperature of the above reaction container was controlled at 80° C., 113 g of MTMS, 194 g of APTS, and 99 g of DMDMS were added to the above reaction container.
[0123]Subsequently, a mixture of 5.4 g of “A-3” and 83 g of deionized water was dripped for 5 minutes, and stirring was performed for 2 hours at the same temperature as described above to perform a hydrolysis condensation reaction, so that a reaction product was obtained. By the analysis of the reaction product using 1H-NMR, it was found that approximately 100% of the...
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