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With regard to potential catalysis mechanism it is of interest to further investigate the structural basis of phosphorylated protein.

由于磷酸化蛋白质在生物体内具有重要的催化作用,因此研究其催化的结构基础非常重要。

This paper describes some PTC and mechanism of phase transfer catalysis.

介绍了相转移催化的一些催化机理,以及近期的一些PTC。

Dawe B%Oswald T Reduced Adsorption and Separation of Blended Surfactants on Sand and Clay Journal of Canadian Petroleum Technology , 1991,02

朴玲钰%付晓%杨雅立%陶国宏%寇元离子液体的酸性测定及其催化的二苯醚/十二烯烷基化反应 10.3321/j.issn:0253-9837.2004.01.011 催化学报, 2004,01

Recently, the progress has been made in the area of extending the light absorption of titanium oxide into visible light region by metal doping, metalloid doping, and photosensitization.

目前TiO2可见光催化的研究取得了一定进展,金属掺杂、非金属掺杂和染料光敏化等方法都不同程度地实现了TiO2可见光催化。

The mechanism of electrocatalytic reduction, the classification and selection of electrode and catalyst and the effect of temperature, current density and pressure on the selective and Faradaic efficiency of reduction are discussed.

介绍了在水溶性介质中利用电化学催化的方法还原CO2的研究现状:电催化还原机理、电极材料催化剂的分类和选择;综述了温度、电流密度以及压力等对还原选择性和法拉第效率的影响;展望了CO2电催化还原方法的研究方向和应用前景。

The catalysis of heteropoly acids in solid state has received much attention owing to their unique acidic and redox activities.

杂多酸作为固体酸催化剂以其优异的催化性能被广泛的应用在酸催化和氧化催化的各种反应体系中。

Domestic and abroad examples are introduced to illustrate the research and development status of both biocatalytic oxidoreduction and hydrolase -mediated enantioselective synthesis.

本文概述了生物催化技术近年来迅速发展的背景、现状和前景,特别谈到酶在手性合成领域的广泛应用;结合国内外实例,分别介绍了生物催化的不对称氧化还原反应和水解酶催化的对映选择性合成两个主要方面的研究与开发动态。

A(C2H5)3N·HCl-induced palladium complex PdL2Cl2 and CuCl2 catalyzed cyclotrimerization reaction of Ethyl Propiolate has been reported for the first time.

报道了一类三乙胺盐酸盐存在下钯PdL2Cl2-CuCl2催化体系催化的丙炔酸乙酯(Ethyl Propiolate,简称EP)环三聚反应。

In the area of selective catalysis, they will soon publish the first examples of stereochemically thoroughly investigated Enantioselective Organo-Autocatalysis, a process that demonstrates conceptually new catalysis design strategy and also provides structurally well-defined small-molecule models that may help explain the origin and maintenance of homochirality fundamental to the functions of biological systems.

在相邻的选择性催化领域,他们即将发表设计发现的首例有机小分子催化的高立体选择性自复制过程(Enantioselective Organo-Autocatalysis),此类反应不仅避免了繁琐的催化剂和产物分离问题,更有意义的是充分利用了产物自身的催化功能,并为分子手性单一性这一生命体根本特征的起源和自发维持提供了第一个简洁的小分子模型系统。

It can be proposed that the TS-1/H〓O〓 catalyzed opening ring reaction of propylene oxide was an heterogeneous catalytic reaction occurred on the active sites on the surface of the catalyst, not an homogeneous reaction catalyzed by H〓.

根据已知的实验结果可以推断,TS-1/H〓O〓催化的PO的开环反应是发生在催化剂表面活性位上的非均相催化反应过程,与H〓催化的均相反应不同。

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