Combining molybdenum carbide with ceria overlayers to boost Mo/CeO2 catalyzed ammonia synthesis

The design of an efficient non-noble metal catalyst is of burgeoning interest for ammonia synthesis. Herein, we report a Mo₂C/CeO₂ catalyst that is superior in ammonia synthesis activity. In this catalyst, molybdenum carbide coexisted with the ceria overlayers which is from the ceria support as the strong metal–support interaction. There is a high proportion of low-valent Mo species, as well as high concentration of Ce³⁺ and surface oxygen species. The presence of Mo₂C and CeO₂ overlayers not only leads to enhancement of hydrogen and nitrogen adsorption, but also facilitates the desorption and exchange of adsorbed species with the gaseous reagents. Compared with the Mo/CeO₂ catalyst prepared without carbonization, the Mo₂C/CeO₂ catalyst is more than sevenfold higher in ammonia synthesis rate. This work not only presents an explicit example of designing Mo-based catalyst that is highly efficient for ammonia synthesis by tuning the adsorption and desorption properties of the reactant gases, but opens a perspective for other elements in ammonia synthesis.     

Unraveling the effect of alumina-supported Y- doped ceria composition and method of preparation on the WGS activity of gold catalysts

The demands for high-purity hydrogen required in fuel-cell applications impose new goals and challenges for design of well performing water-gas shift (WGS) catalysts. Gold-based catalysts have exhibited high activity in the WGS reaction at low temperature. Preparation of appropriate and economically viable supports with complex composition by various synthesis procedures is an attractive approach to WGS performance improvement. The effect of two different preparation methods (wet impregnation or mechanical mixing) and ceria content (10, 20 or 30 wt%) on textural, structural, surface and reductive properties and WGS activity of gold catalysts was studied. Additionally, the role of Y₂O₃ as a promoter of ceria was examined. Long-term stability test was carried out at 260 °C over the most active catalyst. The composition of the best performing sample (composed of about 70 wt% alumina), prepared by mechanical mixing, was considered promising in case of practical applications because of its cost efficiency. The combination of gold nanoparticles and alumina supported Y-doped ceria proved an advantageous approach for developing new catalytic formulations with high effectiveness in clean hydrogen production.     

Ni-Al2O3纳米复合电镀工艺的初步研究

初步研究了复合电镀各工艺条件：电流密度、镀液pH值和温度以及搅拌方式对Al2O3纳米微粒在镍基复合镀层中含量的影响。研究表明：电流密度增大不利于提高镀层中纳米微粒的含量；pH值增大也明显使复合量降低;镀液温度升高，镀层中微粒的复合量随之略有改变；电镀时，加强搅拌或适当改变搅拌方式，可以使复合镀居中的纳米微粒含量提高。还利用扫描电镜及能谱对Ni-Al2O3镀层表面进行了观察与分析。     

改性纳米TiO2光催化降解苯酚活性的研究

在装有紫外光的光催化反应器中，用锐钛型纳米TiO2为光催化剂，进行了苯酚水溶液的光催化降解性能的研究。考察了溶液的pH值、纳米TiO2用量、镍（Ni^2＋）掺杂量、苯酚的初始质量浓度等因素对苯酚水溶液光催化降解过程的影响。结果表明，在pH值为7时，苯酚水溶液的降解率达95％以上，强酸和强碱条件均不利于苯酚的降解。当TiO2用量为50mg，UV辐照40min时，200mL质量浓度为50mg／L的苯酚水溶液的降解率为96．3％；当TiO2用量为150mg，UV辐照60min时，200mL质量浓度100mg／L的苯酚水溶液的降解率为95．8％。镍掺杂增加了TiO2的光催化活性，用质量分数为10％的二氯化镍水溶液掺杂制备的复合光催化剂，苯酚水溶液的降解率比未掺杂时增加13．6％。     

纳米级BaAl_2O_4微粉的制备和性质

分别用溶胶 -凝胶法、低温固相反应法 ,制得了纳米级BaAl2 O4微粉 ,用电镜观察了其形貌和粒径的大小 ,用X-射线衍射仪进行了物相分析 ,测定了其纯度与晶型 ,讨论了制备方法与粒度大小的相互影响     

纳米TiO_2半导体催化活性的研究进展

纳米TiO2半导体催化技术具有广阔的应用前景,近年来半导体光催化已成为功能陶瓷材料、光化学、环境保护、生物技术等领域的研究热点之一。本文简要介绍了近年来国内外纳米TiO2半导体光催化剂的研究进展,主要包括纳米TiO2光催化剂的作用机理及结构的影响;提高催化活性的方法,指出了表面贵金属沉积、复合半导体、金属离子掺杂和表面光敏化是提高催化活性和催化效率的有效途径。     

纳米技术在生物传感器中的应用

介绍了纳米技术在生物传感器中的应用，重点阐述当前发展方向的前沿。     

纳米碳酸钙制备过程中添加剂作用机理探讨

采用鼓泡碳化法 ,在最佳反应温度、反应物浓度的条件下 ,考察了添加剂对产物形状及粒径大小的影响 ,得到了直径为 2 0～ 30nm、长径比在 2 0左右且分散性能良好的针状纳米碳酸钙 ,并对添加剂作用机理进行了分析。     

Effects of strontium gallate additions on sintering behavior of gadolinia-doped ceria

The densification behavior and grain growth of Ce_0.8Gd_0.2O_1.9 ceramics were investigated with the strontium gallate concentration ranging from 0 to 5 mol%. Both the sintered density and grain size were found to increase rapidly up to 0.5 mol% Sr₂Ga₂O₅, and then to decrease with further addition. Dense Ce_0.8Gd_0.2O_1.9 ceramics with 97% of the theoretical density could be obtained for 0.5 mol% Sr₂Ga₂O₅-added specimen sintered at 1250^∘C for 5 h, whereas pure Ce_0.8Gd_0.2O_1.9 ceramics needed to be sintered at 1550^∘C in order to obtain an equivalent theoretical density. The addition of Sr₂Ga₂O₅ was found to promote the sintering properties of Gd₂O₃-doped CeO₂.