Trimethylchlorosilane was prepared from hexamethyldisiloxane by-product in producing 7-ADCA and 7-ACA .

采用 新 的 管 式 反应器装置代替釜式 反应器，将生产7-ADCA和7-ACA的副产物六甲基二硅醚 有效地转化成了 三 甲基氯硅烷。

One-step solvent exchange and surface modification of wet gel were accomplished by reaction of trimethylchlorosilane ( TMCS ) with ethanol pore water and Si-OH group in the wet gel .

通过 TMCS与乙醇、湿凝胶孔隙水及Si-OH基团之间的反应， 使湿凝胶的溶剂交换和表面改性得以在一步完成。

The pure silica mesoporous molecular sieve ( MCM-41 ) was modified on the surface by trimethylchlorosilane in polar solvent ( acetone ) and apolar solvent ( toluene ) .

在极性溶剂（丙酮）或非极性溶剂（甲苯）中， 用 三 甲基氯硅烷对全硅介孔分子筛MCM-41进行了表面修饰。

Trimethylchlorosilane was used in the modification of peat to improve its adsorptive property .

采用 三 甲基氯硅烷 处理泥炭（泥炭 硅烷 化 ），使其吸附性能 得以改善。

Study on Redistribution of Methyltrichlorosilane and Trimethylchlorosilane over AlCl_3 Supported Catalyst

固载AlCl3催化甲基三氯硅烷/ 三 甲基氯硅烷再分配 反应 实验研究

When the HF concentration was large the contact angle reaches to a maximum approximately constant value . ( 3 ) In this paper trimethylchlorosilane and fluosilicic acid solution as raw material the glass super-hydrophobic surface with contact angle 157 ° was prepared successfully by sol-gel method .

溶胶-凝胶法：以 三 甲基氯硅烷和氟硅酸溶液为原料，采用溶胶-凝胶法成功制备了玻璃超疏水表面，接触角达到157。

It can be synthesized with the material of lovastatin hydroxy protecting agent of trimethylchlorosilane and t-butyl lithium instead of pyrrole lithium . The total yield is about 78 % .

以洛伐他汀为原料， 三 甲基氯硅烷为羟基保护基， 用 活泼 的 强 亲 核试剂叔丁基锂代替 当前的吡咯烷锂合成了目标产物新伐他汀，总收率达78%。

Hydrophobic silica ( SiO_2 ) aerogels were prepared from cheap water glass directly modified with surface modifier of hexamethyldisiloxane / trimethylchlorosilane ( HMDSO / TMCS ) without solvent exchange and via ambient drying .

以价廉的水玻璃为原料，通过六甲基二硅氧烷和 三 甲基氯硅烷 混合改性剂对制备的SiO2水凝胶进行表面改性，避免了溶剂交换，并常压干燥得到疏水的SiO2气凝胶。

And the surface wettability influenced by molar ratio drying temperature immersion time drying time of trimethylchlorosilane and fluosilicic acid were investigated .

；并分别研究了 三 甲基氯硅烷和氟硅酸的摩尔配比、干燥温度、浸入时间、干燥时间对其表面润湿性的影响。