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The results showed that hydrogen peroxide, silanols species and TiO〓 didn't have solvolysis activity of propylene oxide. While framework Al, coordinatively unsaturated Ti〓 ions as Lewis acid sites in the framework, Ti-OH and the five member ring active titanium species formed by TS-1, hydrogen peroxide and solvent can catalyze the solvolysis of propylene oxide.

研究结果表明:原料双氧水和TS-1沸石上的SiOH和TiO〓对环氧丙烷溶剂解反应无催化活性;而下列物种对环氧丙烷溶剂解反应具有催化活性:TS-1中的骨架铝,沸石骨架中配位不饱和的Ti〓形成的L酸中心,TS-1水解产生的钛羟基和由TS-1,双氧水和溶剂相互作用所生成的五元环中间活性钛物种。

Liquid-phase epoxidation of allyl chloride with hydrogen peroxide was carried out over Ti-MWW, a novel titanosilicate with the MWW structure, to synthesize epichiorohydrin selectively and effectively. Ti-MWW proved to be superior to the conventional TS-1 catalyst in both catalytic activity and product selectivity. Ti-MWW prefers aprotic solvents of acetone and acetonitrile, both of which can restrain the solvolysis of epichiorohydrin, whereas TS-1 favors a protic solvent of methanol.

研究了具有MWW结构的新一代钛硅分子筛Ti-MWW催化剂对烯丙基氯液相环氧化高效合成环氧氯丙烷的催化性能结果表明,Ti-MWW的催化活性以及产物选择性均优于传统的钛硅分子筛TS-1,对于Ti-MWW,合适的溶剂为非质子性溶剂丙酮和乙腈,在该溶剂中环氧化物不易发生溶剂化开环反应;而对于TS-1,合适的溶剂是质子性溶剂甲醇,但甲醇可导致醇醚副产物的生成。

In the second part of the thesis, we developed a very effective assay for the sulfotransferase that catalyzes the sulfation of serine and threonine. It utilized PAPS regenerated from 3-phosphoadenosine 5-phosphate by a recombinant PST using 4-methylumbelliferyl sulfate as the sulfuryl group donor. The change in the fluorescence intensity of 4-methylumbelliferone corresponded directly to the amount of active protein sulfotransferase.

第二部份则是探讨蛋白质亚硫酸转移酵素的活性检测方法,检测系统的主旨是用重组的PST催化受质4-methylumbelliferyl sulfate做为亚酸基提供者并转移至3'-phosphoadenosine 5'-phosphate再生PAPS ,此核苷酸的亚酸基再由蛋白质亚硫酸转移酵素催化,反应后所产生的4-methylumbelliferone之萤光变化可用来定量蛋白质亚硫酸转移酵素的活性。

In order to investigate the activity of bi-CoSPc to the higher thiol oxide, the 1-octanethiol oxidation rate was determined, the result showed that, the rate of 1-octanethiol oxidation increased with rising of reaction temperature, concentration of catalyst, and concentration of alkali.

结果表明:在相同反应条件下,与CoSPc相比,bi-CoSPc对正辛硫醇的氧化过程具有更高的催化活性;反应温度的升高,催化剂浓度的增加及碱液浓度的提高,均有利于硫醇的催化氧化反应。

By using isothermal DSC, we obtained the relationship of , and , and by using a non-linear fitting algorithm, we obtained the value of the parameters of the curing kinetics equation, found that the autocatalytic kinetics model with independent reaction order and was more similar with the experimental result then that of .

通过等温DSC分析了不同温度下树脂固化反应的自催化动力学模型,研究了,以及的关系,并通过非线性最小二乘法模拟求出了固化动力学方程的各参数,认为和互相独立的自催化动力学模型比的模型更好地适合于乙烯基酯树脂中高温固化反应的实验结果。

Fe-ion doped TiO2 was immobilized on solid support stubstrates-SiOa using sol-gel method. The photocatalytic efficiency of the TiO2 coating was compared with nanosize powders using the degradation of benzophenol in a aqueous solution as a standard test system, the photocatalytic efficiency was found to markedly increase.

采用溶胶凝胶法制备了硅胶附载的掺杂不同量铁离子的二氧化钛薄膜,用XRD,Raman,SEM的手段进行了表征,证明该条件下制备的二氧化钛为锐钛矿相,薄膜在硅胶表面的成膜效果较好,但有一定程度的龟裂,通过光催化实验发现催化效率与纳米粉相比有明显的提高。

The studies are significant to propose the synthetic methodology of benzothiazole derivatives,broaden the application of the metal complexes of benzothiazoles.It is practical value of the research in preparation of phenylacetic acid from metal-catalyized carbonylation.The thesis consists of four chapters.

本论文研究了苯并噻唑衍生物及其钴、铑金属配合物的合成,并研究了两类金属配合物的羰基化催化性能,提供了合成苯并噻唑衍生物的可行路线,拓宽了苯并噻唑金属配合物的应用范围,催化羰基化合成苯乙酸的研究具有重要的实用价值。

Template-confined growth is a very powerful method for obtaining aligned 1D nanomaterials with adjustable diameter, length and morphology. Porous anodic aluminum oxide templates with different channel structures have been synthesized in our lab, with which the aligned CNT arrays, Y-branching and novel dendriform CNTs have been obtained. Based on the structural characterization of the products, a space-limited and self-catalytic growth mechanism has been proposed accordingly. Roughly speaking, the catalyst particles at the bottom of template channels initiate the nucleation of carbon species, which acts as the seed for subsequent CNT growth.

本文采用近年发展起来的模板控制生长法,以多孔氧化铝模板控制CVD生长的方法调控了碳纳米管有序阵列、γ-分叉及树枝状分叉结构,在对产物进行详尽结构表征和分析的基础上阐述了氧化铝模板控制生长碳纳米管的生长机制:孔道内催化剂仅在生长初始阶段催化碳物种的成核,起&种子&作用,随后模板孔道自身的催化及限域作用使碳纳米管紧贴着孔道内壁生长。

The reason may be that complex formed by rhodium and halide was difficult to produce the catalytic active species. Therefore halide ion was the poison for the rhodium catalyst in hydroformylation of olefins in ionic liquid. The effect of double long chain cationic surfactant (DCMAB, dicetyl dimethylammonium bromide) on selective hydrogenation of cinnmaldehyde catalyzed with RuCl3·x H2O/TPPTS was studied.

进一步的研究表明在使用有良好反应活性的两种催化剂HRh3 、Rh_2进行催化反应时,向体系中加入含有卤离子的化合物时将使反应活性大大降低,而且随着卤化物加入量的增加,催化剂的活性迅速下降,这是卤离子可能和金属铑作用使它难于生成催化活性物种,进一步证明卤素离子是引起催化剂活性下降的极其重要的因素。

The catalytic performance of all the amorphous alloy catalysts mentioned above was measured during liquid phase hydrogenation of furfural to furfuryl alcohol, together with the kinetic studies. The relationship between the catalyst performance and the structure of catalyst, surface electronic state of the amorphous alloy has been systematically studied based on a series of characterization of catalysts . Meanwhile, the promoting effects of the support on the thermal stability and catalytic activity of the amorphous alloy catalysts have been discussed.

本文采用一系列的表征方法(XRD、XPS、TEM、BET、氢吸附、TPD等)进一步研究非晶态合金催化剂的表面结构、表面电子态和催化性能之间的关系,探索电子效应和几何效应对催化剂活性中心结构的影响,探索非晶态合金的晶化失活和载体对非晶态结构的稳定化作用,以及修饰剂对催化性能的改善作用等。

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