首页> 外文期刊>Journal of the American Chemical Society >MECHANISM OF SOLID/LIQUID INTERFACIAL REACTIONS - THE HYDROLYTIC DISSOLUTION OF SOLID TRIPHENYLMETHYL CHLORIDE IN AQUEOUS SOLUTION
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MECHANISM OF SOLID/LIQUID INTERFACIAL REACTIONS - THE HYDROLYTIC DISSOLUTION OF SOLID TRIPHENYLMETHYL CHLORIDE IN AQUEOUS SOLUTION

机译:固/液界面反应的机理-固体三苯甲基氯在水溶液中的水解

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摘要

The reaction between solid triphenylmethyl chloride (TPMCl) and water, TPMCl(s) + H2O(1)-->TPMOH(aq) + H+(aq) + Cl-(aq), where TPMOH is triphenylmethyl alcohol, has been investigated using the channel flow cell method. It is found that hydrolysis proceeds via a direct heterogeneous fashion whereby the reaction occurs at the solid-liquid interface rather than in solution after the prior dissolution of TPMCl. Kinetic parameters are reported including the effect of ionic strength. Further, using experiments conducted with different surfaces of single crystals of TPMCl, it is shown that the rate of the interfacial process depends on the availability of exposed chlorine atoms in the reacting crystal plane. In situ atomic force microscopic studies indicate that the TPMCl surface, once in contact with water, is covered rapidly by a porous product layer, However, the latter provides a negligible effect on the reaction rate because of its high porosity.
机译:已使用以下方法研究了固体三苯甲基氯(TPMCl)与水TPMCl(s)+ H2O(1)-> TPMOH(aq)+ H +(aq)+ Cl-(aq)之间的反应,其中TPMOH是三苯甲醇通道流动池法。发现水解以直接的非均质方式进行,由此反应发生在固-液界面而不是在TPMC1预先溶解后的溶液中。报告了动力学参数,包括离子强度的影响。此外,使用对TPMC1的单晶的不同表面进行的实验,表明界面过程的速率取决于反应的晶体平面中暴露的氯原子的可用性。原位原子力显微镜研究表明,TPMC1表面一旦与水接触,就会迅速被多孔产物层覆盖,但是,由于其高孔隙率,后者对反应速率的影响可忽略不计。

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