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Bismuth oxyhalide compounds show better photocatalytic activities than TiO2 (P25). With the increasing of X atomic numbers, photocatalytic activities of BiOX are enhanced in sequence.

卤氧化铋的光催化活性普遍优于商品TiO2 (P25)的光催化活性,并且随着卤素原子序数的增加光催化活性逐渐增强。

Kinetic reaction behavior of neo- polyhydric alcohols with fatty acids catalyzed by sulfuric acid was studied.

比较了Brnsted酸,包括硫酸、磷酸、对甲苯磺酸,催化季戊四醇与脂肪酸的酯化反应行为,结果表明,硫酸催化酯化反应速率最快,能有效催化不同类型的新戊基多元醇与脂肪酸的酯化反应,羟基转化率达到98%以上。

The result of the test showed that the fed quantity of TiO2 was 1.25 mg/mL,the photocatalytic degradation of the pyridine was in conformity with the first order kinetic equation,the feeding of 0.2%H2O2 obviously increased the degradation rate of the pyridine and the nitrogen in the pyridine converted into ammonia nitrogen;the pearlite-loaded TiO2 had the same catalytic effect as that of powered TiO2 and was easy to recover and reutilize.

以钛酸四丁酯水解法制备TiO2,采用溶胶一凝胶法在膨胀珍珠岩上负载TiO2,在UV-TiO2体系中对水中吡啶进行光催化降解,结果表明:TiO2加入量为1.25mg/mL,吡啶的光催化降解符合一级动力学方程,加入0.2%H2O2可明显加快吡啶的降解速度,吡啶中氮转化为氨氮,珍珠岩负载型TiO2与粉末TiO2具有相同的催化效能,且便于回收和重复使用。

According to studying the factors of using a series of rhodanine ramifications to determine metal ions by catalytic fluorescence method and by utilizing the strong catalysis of metal ions to potassium periodate oxygenating rhodanine, a catalytic fluorescence method of using the new type rhodanine ramifications to determine trace tin, antimony and cobalt was established.

首次研究了系列若丹宁衍生物在催化荧光法测定金属离子中的各影响因素,利用痕量金属离子对高碘酸钾氧化若丹宁具有强烈催化作用的性质,建立了新型若丹宁物质催化荧光法测定痕量锡、锑、钴的新方法。

A few spiro ligands have been successfully synthesized and applied in asymmetric catalysis .

手性螺环配体的合成及其在不对称催化反应中的应用是不对称合成和催化研究中重要的研究领域之一,一些手性螺环配体被合成出来并成功地应用于不对称催化反应中。

In this study, a new idea that RDF is made with catalysis of alkali,alkali earth or transition metal salts. The addition of the catalysts is to low ignition and burn off temperature temperature.

本课题提出在制备RDF过程中引入催化助燃剂的新思路,这些催化助燃剂包括了许多碱或碱土金属的化合物,同时也考虑一些过渡金属的催化作用。

Photocatalytic activity of the catalyst was investigated for microwave assisted photocataqlytic degradation of acid mordant red B dye in aqueous solution.

通过可溶性染料酸性媒介红 B的微波辅助光催化氧化反应,考察了其光催化活性;并研究了复合催化剂的煅烧温度、铈掺杂量和涂覆次数等对催化活性的影响。

Research activities also include synthesis and modification of biological-relevant intermediates, cofactors and their corresponding analogs, for elucidation of enzymatic mechanisms.

具体内容包括生物催化体系关键中间体和辅助因子及其类似物的化学合成和修饰;生物催化体系的重建;酶催化反应的机理和生物催化剂工程等。

The color fading reation on potassium bromate with Victoria green stand G by the catalysis of nitrite in hydrochloric acid medium was studied.

采用流动注射技术与催化光度法相结合,研究了亚硝酸根催化溴酸钾氧化维多利亚绿G的高灵敏度褪色反应,用自制的微机化流动注射分析仪能准确控制时间,优化了实验条件,建立了测定痕量亚硝酸根的流动注射催化光度方法。

In this paper, as a typical lewis acid, anhydrous aluminum (AlCl_3) was used as the catalyst to get PP/PS blends compatibilized by in-situ Fridel-Crafts alkylation. The effects on PP and PS components of AlCl_3 were investigated first, mainly by rheology, including steady rheology method and dynamic rheology method. Then the in-situ reactions in PP/PS alloys under different conditions were executed and studied in detail by selective Soxhlet solvent extraction. And at the same time, the evolutions of phase structures of PP/PS and the resulted PP/PS/AlCl_3 alloys were investigated by SEM and SALS. The steady and dynamic rheological behaviors of in-situ compatibilized PP/PS alloys were obtained systematically.

本文选用典型路易斯酸无水氯化铝(AlCl_3)作为催化剂,利用烷基化反应机理,对PP/PS合金直接进行原位催化反应增容,以流变学方法(包括静态流变和动态流变学方法)为主,详细探讨无水AlCl_3对PP/PS合金体系中PP和PS两组分的影响,并在此基础上进一步系统研究无水AlCl_3原位催化增容PP/PS合金的相结构演变及增容反应特征,然后对不同原位催化增容条件下获得增容合金材料的流变行为特征作了深入探讨。

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