A global inventory of nitric oxide emissions from soils

Over 60 published papers reporting field measurements of emissions of nitric oxide (NO) from soil are reviewed, and over 100 annual estimates of NO emissions were made for various types of ecosystems, including agricultural fields. These data were stratified by biome and the mean of each stratum was multiplied by an estimate of the biome area. A few strata were identified as clearly having low NO emissions: montane forests, swamps and marshes, tundra, and temperate forests that are not heavily affected by N deposition. The largest emissions were observed in tropical savanna/woodland, chaparral, and cultivated agriculture, but variation in NO emissions within these strata was also large. Although the stratification scheme fails to partition this within-stratum variation, it does clearly identify these biomes as globally important sources of NO and as areas where more research is needed to investigate within-biome variation in NO emissions. It is too early to tell whether differences in NO emissions between temperate and tropical agriculture are significant, but it is clear that agriculture is an important source of NO and that management practices affect NO emissions. The best current estimate of the global soil source of NO is 21 Tg N yr^-1. Adsorption of NO_x onto plant canopy surfaces may reduce emissions to the atmosphere to as low as 13 Tg N yr^-1, although the absorption effect is probably smaller than this. An error term for the global estimate is difficult to determine, but it is at least ±4 and perhaps as large at ±10 Tg N yr^-1. Hence, only modest progress has been made in narrowing uncertainties in the estimate of the global soil source of NO, although some published lower estimates appear unlikely. This inventory reconfirms that the soil source of NO is similar in magnitude to fossil fuel emissions of NO_x. Further narrowing of the uncertainty of the estimate of global soil NO emissions will require more sophisticated and carefully chosen stratification schemes to address variation within biomes based on soil fertility, soil texture, climate, and management and will require linking this type of inventory and stratification with mechanistic models.     

Co–Pd/γ‐Al2O3 catalyst for heavy oil upgrading: Desorption kinetics,reducibility and catalytic activity

The influence of Pd on a Co–Pd/γ‐Al₂O₃ heavy oil upgrading catalyst is investigated using different physicochemical and reactive Characterization techniques. Nitrogen adsorption isotherm analysis shows that the specific surface area and porosity of the support alumina is significantly decreased due to the blockage of the pores by the loaded cobalt species. The estimated activation energy of NH₃ desorption is found to be less for Co–Pd/γ‐Al₂O₃ sample, which confirms improved acidity due to Pd. TPR experiments show that the reducibility of the catalyst is significantly improved with the presence of Pd. Higher metal dispersion and hydrogen spillover effects are the main reasons for the enhanced reducibility of the Pd promoted catalyst as revealed by the H₂‐pulse chemisorptions study. When evaluated using VGO as feed stock, the Co–Pd/γ‐Al₂O₃ displayed superiority both in hydrodesulphurisation (HDS) and hydrocracking (HC) activities as compared to the unpromoted Co/γ‐Al₂O₃ catalyst. The coke deposition on the spent catalyst is also found to be low due to the Pd promotional effects. This is an encouraging result, given that higher hydrogenation activity of the catalyst can be achieved without compromising the cracking activity and sustained activity of the catalyst.     

Multifunctional Nanochemistry: Ambient,Electroless, Template-Based Synthesis and Characterization of Segmented Bimetallic Pd/Au and Pd/Pt Nanowires as High-Performance Electrocatalysts and Nanomotors

Segmented noble-metal nanowires (NWs) represent an exciting, multifunctional, one-dimensional, structural architecture with a variety of potential applications. However, the widespread use of electrodeposition in the preparation of these systems has limited their potential to be produced on a large scale, since this protocol is costly and requires complex processes and caustic reaction media. Given the inherent limitations of electrodeposition, we report, for the first time, an ambient, surfactantless, template-based approach that is not only sustainable but also efficient for the reliable production of Pd/Pt and Pd/Au segmented NWs, possessing two spatially separated, chemically distinctive, but elementally pure, axial subunits. Our simple two-step synthetic approach allows for direct and predictable control over the relative segment lengths in these nanomaterials. Moreover, thorough structural characterization of these as-prepared samples confirms that our segmented NWs maintain high-quality, crystalline, elementally pure subunits with a well-defined interface between the constituent metals. In the context of preparing segmented NWs as multifunctional nanostructures, we demonstrate that these as-prepared NWs achieve high levels of performance when employed as both electrocatalysts and nanomotors.     

LaCoO3 acts as a high-efficiency co-catalyst for enhancing visible-light-driven tetracycline degradation of BiOI

Exploring noble-metal-free co-catalysts highly flexible for separating the photogenerated charge carriers is of prime importance for the visible-light-driven photocatalysis. Herein, three-dimensional flower-like BiOI microspheres were fabricated and applied to support noble-metal-free LaCoO₃ co-catalysts to construct a unique LaCoO₃/BiOI hybrid photocatalyst with a higher ability in charge separation. As expected, the optimum tetracycline degradation rate of LaCoO₃ (4.0 wt%)/BiOI was up to 0.0161 min⁻¹, which was nearly 3.4 fold larger than that of pure BiOI (0.0048 min⁻¹). The enhanced photocatalytic performance was mainly ascribed to the vital role of LaCoO₃ co-catalyst, which acted as an excellent electron collector for capturing the electrons generated by BiOI, effectively promoting the separation of photogenerated charge carriers and prolonging the lifetime of photo-induced electron-hole pairs at the same time. Furthermore, the active species trapping experiments revealed that the excellent photocatalytic activity was primarily driven by photogenerated holes and superoxide radicals. This work is expected to provide a new inspiration for rationally designing and fabricating noble-metal-free co-catalyst system with high efficiency applied in environment purification.     

湖南铜山岭矽卡岩型伴生金银矿的地质地球化学特征

铜山岭矽卡岩型铜-多金属伴生金银矿床,产于燕山期花岗闪长岩与泥盆系碳酸盐岩的接触带中。金主要呈自然金形式产于黄铜矿和黄铁矿等硫化物中;银主要呈自然银、辉银矿和含硫盐产于方铅矿等硫化物内。金-铜、银-铅密切相关。成矿物质主要不是来自围岩,而是来自深部。成矿与构造-岩浆活动有关。     

Measurement and modelling of the interfacial tension of triglyceride mixtures in contact with dense gases

The interfacial tension of various triglyceride mixtures in contact with carbon dioxide is compared. The interfacial tension of these triglyceride mixtures is similar. The interfacial tension in contact with carbon dioxide and nitrogen decreases with increasing pressure. Concerning the interfacial tension in contact with carbon dioxide, the interfacial tension increases at higher pressure with rising temperature. The interfacial tension of triglyceride mixtures and of many other liquids in contact with carbon dioxide can be described as a function of the carbon dioxide density.The modelling of the interfacial tension of triglycerides in contact with carbon dioxide or nitrogen using the density gradient theory (Macromolecules 14 (1981) 361) and the Sanchez-Lacombe equation of state (J. Phys. Chem. 80 (1976a/b) 2352 and 2568) is successful if one parameter for nitrogen and two parameters for carbon dioxide are employed. Nevertheless, an appropriate equation of state must be utilized for modelling the interfacial tension of a system. For complex systems, e.g. for triglyceride mixtures, it is indispensable to check the equation of state by means of experimental equilibrium data (e.g. density, volume, or mole fraction).     

微生物法处理含硫工业废气

指出了含硫工业废气传统处理方法的缺陷 ,介绍了微生物处理方法的优势所在 ;对微生物菌种的共同特征以及无机硫和有机硫脱除时菌种的选择依据进行了讨论 ,并对微生物法脱硫的机理进行了分析 ;评述了国内外生物滤池法、生物滴滤池法和生物吸收法等生物膜法脱硫的工艺及其工业化应用。指出了微生物法脱硫技术有待深入研究的问题、发展趋势和应用前景。     

Effect of Water Vapor on the Release of Fission Gases from Uranium Oxycarbide in High-Temperature, Gas-Cooled Reactor Coated Fuel Particles

The hydrolysis of uranium oxycarbide (UCO) was studied by injecting water vapor into a fuel element containing a known number of high-temperature, gas-cooled reactor (HTGR) coated particles with exposed fuel kernels. The experiments were conducted in the High Flux Isotope Reactor (HFIR) at temperatures between 700° and 1000°C, a system pressure of 200 kPa, and partial pressures of water vapor between 21 and 199 Pa. The general sequential response of the exposed fuel kernels to water vapor addition consisted of (1) a rapid release of stored fission gas with a concomitant increase in the steady-state release and (2) a period of constant steady-state release. Upon cessation of the addition of water vapor, a decline in the release to prehydrolysis values generally occurred. The release of stored fission gas was dependent on the square of the partial pressure of water vapor. The ratio of the constant steady-state release to the prehydrolysis value was independent of the partial pressure of water vapor. The time constant for the decline in the release was the same in all of the hydrolysis tests.     

含氮化合物废气选择性催化氧化技术研究进展

通过对当前含氮化合物废气治理技术的对比分析,总结选择性催化氧化的相关技术优势。根据对含氮化合物的种类及来源分析,介绍氨气、腈类、胺类及其他含氮化合物的催化净化技术。重点总结催化剂的种类、研发进展和在实际使用中可能遇到的问题,同时展望含氮化合物废气选择性催化氧化技术的研发方向。     

汽车尾气用催化剂载体研究现状及展望

汽车尾气催化净化器中，催化剂载体是实现高效尾气净化的一个关键因素。本文综述了对尾气净化催化剂载体的要求和研究现状。并提出导电型复合陶瓷是今后尾气净化载体材料研究和发展的一个新型方向。