Development of catalysts for hydrogen generation from hydride compounds

Catalytic hydrolysis of NaBH₄ and NH₃BH₃ has been studied. It was shown that the nature of the support and the active component of the catalyst affect the H₂ generation rate. Despite similar sizes of rhodium particles formed on the surface of different supports (γ-Al₂O₃, TiO₂, carbon), their reactivity is different. Rh/TiO₂ with low rhodium concentration (1 wt.%) is the most active catalyst both in the hydrolysis of NaBH₄ and NH₃BH₃. The obtained results show that the rhodium chloride interaction with titania determines the reactivity of rhodium particles formed under action of NaBH₄ medium. TEM, DRS UV–vis and XPS were used to characterize the catalysts.     

硫酸钙氨法制取硫酸钾新工艺的实验研究

利用K2 +2 ,Ca2 +/ /SO2 -4 ,Cl2 -2 ,NH3—H2 O混合体系相图作为工艺指导 ,进行硫酸钙制取硫酸钾工艺的相图研究和分析 ,确定实验优选因素及水平并进行正交实验 ,根据实验结果进行极差分析 ,得出新的结论。合适的工艺条件为 :氨浓度为 40 % ,配料比n( 2KCl) :n(CaSO4 ·2H2 O)为 1:1,反应温度为 5℃ ,反应时间为 1h。     

Reactively sputtered MoO3 films for ammonia sensing

We report the gas-sensing properties of ion-beam sputter deposited MoO₃ thin-films. The change in the DC conductivity was measured in dry N₂ with 10% O₂ in the presence of up to 490 ppm of NH₃, NO, NO₂, C₃H₆, CO and H₂. At ∼440 °C the film was found to be very sensitive to NH₃, with 490 ppm increasing the conductivity by approximately a factor of 70. This was approximately 17 times greater than the response to the other gases. The NH₃ response was strongly affected by the accompanying levels of O₂, NO₂ and H₂O. For example, changing the accompanying O₂ levels from 1% to 20% decreased the NH₃ response by approximately a factor of 20. Similarly, the presence of 100 ppm NO₂ (in 10% O₂) decreased the NH₃ response by approximately a factor of three, and 1% water vapor decreased it by more than a factor of two. The NH₃ response, however, was relatively unaffected by 100 ppm of accompanying NO, C₃H₆, CO or H₂. XPS measurements show that the increased conductivity in the presence of NH₃ was also accompanied by a partial reduction of the surface MoO₃. We observed an increase in the resistance of the films after extended time at elevated temperatures.     

粘接低表面能材料的新型胶粘剂研究

详述了用于低表面能材料粘接的新型胶粘剂的制备过程,探讨了低表面能胶粘剂的粘接机理,并讨论了弹性体、三乙基硼烷胺络合物、丙烯酸单体等对低表面能材料胶粘强度的影响.     

A model of ammonia volatilisation from a dairy farm: an examination of abatement strategies

A model (MAST) to calculate the mass flow of NH₃ through amodel dairy farm has been developed. Updated emission factors for UKagriculturewere used to examine different abatement strategies available for a typicaldairy farm. A range of annual NH₃ emissions was calculated for bothslurry and FYM based dairy systems. Emission for the slurry based system ranged between 27 kg NH₃-N ha^–1 yr^–1, achieved using a combination of abatementstrategies, and 107 kg NH₃-N ha^–1 yr^–1, calculated for a worst casescenario. For FYM, this range was between 33 and 86 kg NH₃-Nha^–1 yr^–1. The greatest reductionswereachieved by manipulating options linked to fertiliser usage and manureapplication.     

氨合成催化剂钝化的研究

探索了氨合成催化剂还原后的温度对钝化操作与产品质量的影响,确定了最佳的钝化温度。     

C．F．布朗深冷净化系统模拟分析

通过模拟计算对深冷净化系统做了深入的分析，研究了深冷净化系统脱除甲烷化气中过量氮、甲烷、惰气和回收弛放气中氢的能力，甲烷化气组成和压力对净化效果和操作稳定性的影响。     

Pt-V2O5-WO3/TiO2 catalysts supported on SiC filter for NO reduction at low temperature

The catalytic filter, V₂O₅-WO₃-TiO₂ supported on a ceramic filter, is known as a promising material for treating particulates and NO _x simultaneously at optimum temperatures around 320°C. In order to improve its catalytic activity at low temperatures, the effect of Pt addition on the catalytic filter has been investigated. Catalytic filters, Pt-V₂O₅-WO₃-TiO₂/SiC, were prepared by co-impregnation of Pt, V, and W precursors on TiO₂ coated-SiC filter by vacuum aided-dip coating. The Pt-added catalytic filter shifted the optimum working temperature from 280–330°C (for the non Pt-impregnated filter) to 180–230°C, providing N _x slip concentration less than 20 ppm for the treatment of 700 ppm NO at a face velocity of 2 cm/s with the same value over the non Pt-added catalytic filters. The promotional effect following the addition of Pt is believed to result from electrical modification of the catalyst maintaining a high electron transfer state. Ammonia oxidation was also observed to be dominant above the optimal temperature for SCR.     

二氧化碳激光熔铸技术在氨压缩机曲轴修复中的应用

用连续输出功率在千瓦级的二氧化碳激光器 ,激光功率密度达到 (10 4～ 10 5)W·cm-2 时 ,对铁基材料表面进行熔铸 ,讨论了激光熔铸修复工艺 ,论述了对修复件强度、表面硬度和抗磨性能、残余应力的影响。     

AMMONIA CATALYZED ORGANOSOLV DELIGNIFICATION OF POPLAR

A parametric investigation of NH₄OH catalyzed solvent delignification of poplar was conducted to define pretreatment conditions which would yield an optimal separation of the biomass components and an enzymatic susceptible solid carbohydrate phase. Delignification parameters of interest included concentration of NH₄OH, time and temperature of the reaction, and type of solvent. The addition of 0.82 M NH₄OH to the delignification liquor increased lignin removal and decreased carbohydrate degradation, but increasing NH₄OH concentration had no additional effect. At lower reaction temperatures, the extent of delignification increased with reaction time; at higher temperatures, a “relignification” of the pretreated wood was observed. The delignification and hemicellulose solubilization were modelled and rate constants reported. No major difference between three potential pulping solvents—ethanol, butanol, phenol—was observed. The enzymatic susceptibility of pretreated wood samples was approximately 6-fold greater than that of the untreated poplar. UV absorbance was used to qualitatively characterize the soiubilized lignins.