普通小球藻和铜绿微囊藻与粘土颗粒凝聚沉降行为研究

本研究结果表明,不同的藻类和不同的粘土颗粒均使藻类与粘土颗粒的凝聚沉降发生变化。结果还表明,溶液中[Cu~(2+)]浓度超过10~(-5)mol后,加快了小球藻与高龄土的凝聚沉降。使80％以上的小球藻和高岭土在不到10min内即凝聚沉降。在最后结合实验结果讨论了利用藻类与粘土的凝聚沉降治理水体污染。     

Fenton-混凝法处理焦化废水的试验研究

对Fenton预氧化-混凝法联用技术处理焦化废水进行了研究,探讨了Fenton氧化阶段H2O2投加量、混凝阶段pH值以及混凝剂投加量等因素对焦化废水COD去除率的影响,确定了最佳处理条件.结果表明,Fenton预氧化-混凝法处理焦化废水取得了良好效果,COD去除率达97.5%,为该工艺实际处理焦化废水提供了实验依据.     

Concurrent catalytic removal of typical volatile organic compound mixtures over Au-Pd/α-MnO2 nanotubes

α-MnO_2 nanotubes and their supported Au-Pd alloy nanocatalysts were prepared using hydrothermal and polyvinyl alcohol-protected reduction methods, respectively. Their catalytic activity for the oxidation of toluene/m-xylene, acetone/ethyl acetate, acetone/m-xylene and ethyl acetate/m-xylene mixtures was evaluated. It was found that the interaction between Au-Pd alloy nanoparticles and α-MnO_2 nanotubes significantly improved the reactivity of lattice oxygen, and the 0.91 wt.% Au0.48 Pd/α-MnO_2 nanotube catalyst outperformed the α-MnO_2 nanotube catalyst in the oxidation of toluene, m-xylene, ethyl acetate and acetone. Over the0.91 wt.% Au0.48 Pd/α-MnO_2 nanotube catalyst,(i) toluene oxidation was greatly inhibited in the toluene/m-xylene mixture, while m-xylene oxidation was not influenced;(ii) acetone and ethyl acetate oxidation suffered a minor impact in the acetone/ethyl acetate mixture; and(iii) m-xylene oxidation was enhanced whereas the oxidation of the oxygenated VOCs(volatile organic compounds) was suppressed in the acetone/m-xylene or ethyl acetate/m-xylene mixtures. The competitive adsorption of these typical VOCs on the catalyst surface induced an inhibitive effect on their oxidation, and increasing the temperature favored the oxidation of the VOCs. The mixed VOCs could be completely oxidized into CO_2 and H_2 O below 320°C at a space velocity of 40,000 m L/(g·hr). The 0.91 wt.% Au0.48 Pd/α-MnO_2 nanotube catalyst exhibited high catalytic stability as well as good tolerance to water vapor and CO_2 in the oxidation of the VOC mixtures. Thus, the α-MnO_2 nanotube-supported noble metal alloy catalysts hold promise for the efficient elimination of VOC mixtures.     

Preparation of ceria-zirconia solid solution with enhanced oxygen storage capacity and redox performance

A new method called ultrasonic-assisted membrane reaction (UAMR) was reported for the fabrication of ceria-zirconia solid solution. A series of ceria-zirconia solid solutions with different Ce/Zr molar ratios were prepared by the UAMR method and characterized by X-ray diffraction (XRD), N₂ adsorption, hydrogen temperature-programmed reduction (H₂-TPR), scanning electron microscope (SEM), and transmission electron microscopy (TEM) techniques. The UAMR method proved to be superior, especially when the Ce/Zr molar ratio was lower than 1, in fabricating ceria-zirconia solid solutions with large BET surface area, high oxygen storage capacity (OSC), and low reduction temperature.     

A comparative investigation of NdSrCu_(1-x) Co_x O_(4-δ) and Sm_(1.8) Ce_(0.2) Cu_(1-x) Co_x O_(4-δ) (x:0–0.4) for NO decomposition

A series of single-phase T-structured NdSrCu 1-x Co x O 4-δ with oxygen vacancies and T -structured Sm 1.8 Ce 0.2 Cu 1-x Co x O 4-δ (x: 0–0.4) with oxygen excess were prepared using ultrasound-assisted citric acid complexing method, and characterized by means of techniques such as thermogravimetric analysis and NO temperature-programmed desorption (NO-TPD). The catalytic activities of these materials were evaluated for the decomposition of NO. It was found that the NdSrCu 1-x Co x O 4-δ catalysts were of oxygen vacancies whereas the Sm 1.8 Ce 0.2 Cu 1-x Co x O 4-δ ones possessed excessive oxygen (i.e., over-stoichiometric oxygen); with a rise in Co doping level, the oxygen vacancy density of NdSrCu 1-x Co x O 4-δ decreased while the over-stoichiometric oxygen amount of Sm 1.8 Ce 0.2 Cu 1-x Co x O 4-δ increased. The NO-TPD results revealed that NO could be activated much easier over the oxygen-deficient perovskite-like oxides than over the oxygen-excessive perovskite-like oxides, with the NdSrCuO 3.702 catalyst showing the best efficiency in activating NO molecules. Under the conditions of 1.0% NO/helium, 2800 hr -1 , and 600–900°C, the catalytic activity of NO decomposition followed the order of NdSrCuO 3.702 NdSrCu 0.8 Co 0.2 O 3.736 NdSrCu 0.6 Co 0.4 O 3.789 Sm 1.8 Ce 0.2 Cu 0.6 Co 0.4 O 4.187 Sm 1.8 Ce 0.2 Cu 0.8 Co 0.2 O 4.104 Sm 1.8 Ce 0.2 CuO 4.045 , in concord with the sequence of decreasing oxygen vacancy or oxygen excess density. Based on the results, we concluded that the higher oxygen vacancy density and the stronger Cu 3+ /Cu 2+ redox ability of NdSrCu 1-x Co x O 4-δ account for the easier activation of NO and consequently improve the catalytic activity of NO decomposition over the catalysts.     

Efficient Delineation of Nested Depression Hierarchy in Digital Elevation Models for Hydrological Analysis Using Level‐Set Method

In terrain analysis and hydrological modeling, surface depressions (or sinks) in a digital elevation model (DEM) are commonly treated as artifacts and thus filled and removed to create a depressionless DEM. Various algorithms have been developed to identify and fill depressions in DEMs during the past decades. However, few studies have attempted to delineate and quantify the nested hierarchy of actual depressions, which can provide crucial information for characterizing surface hydrologic connectivity and simulating the fill‐merge‐spill hydrological process. In this paper, we present an innovative and efficient algorithm for delineating and quantifying nested depressions in DEMs using the level‐set method based on graph theory. The proposed level‐set method emulates water level decreasing from the spill point along the depression boundary to the lowest point at the bottom of a depression. By tracing the dynamic topological changes (i.e., depression splitting/merging) within a compound depression, the level‐set method can construct topological graphs and derive geometric properties of the nested depressions. The experimental results of two fine‐resolution Light Detection and Ranging‐derived DEMs show that the raster‐based level‐set algorithm is much more efficient (~150 times faster) than the vector‐based contour tree method. The proposed level‐set algorithm has great potential for being applied to large‐scale ecohydrological analysis and watershed modeling.     

基于FTA的尿素热解脱硝系统可靠性分析

为提高尿素热解脱硝系统可靠性水平,通过分析系统组成和各种可能的失效情况,以尿素热解脱硝系统不能正常工作为顶事件建立了故障树,对其进行定性分析,求取了故障树的最小割集。同时在此基础上分析了各个基本事件的结构重要度,明确了导致尿素热解脱硝系统失效的主要影响因素,并对其相应的解决措施进行了探讨。     

AB工艺污水厂A段不同溶解氧运行效果

对AB工艺城市污水处理厂A段不同溶解氧工况下的实际运行效果进行了监测分析。结果表明:A段按设计参数兼氧运行对BOD5、COD、SS的去除率最高,平均分别达到59.4%、77.2%、73.2%;总氮的去除率随A段溶解氧含量影响不大,平均为46.8%;总磷的去除率随溶解氧含量的增大而升高,最高可达80.2%。     

Hydraulics Analysis for Groundwater Flow Through Permeable Reactive Barriers

Groundwater flow modelling is an important tool in simulating and predicting hydraulic behaviour of groundwater transporting in the domain consisted of groundwater flow zone (aquifer) and permeable reactive barriers (PRBs). The aquifer regime is modelled using the Darcy equation, whereas PRBs are simulated by the Brinkman equation. By combining the above equations, the present paper is devoted to analyse the effect of permeability of aquifer (K _aq ) and reactive media (K _p ), groundwater flow velocity, and barrier size as well as assembled style of barriers on key barrier design parameter, such as the hydraulic capture zone width. The simulations indicate that the capture zone width generally decreases with a decrease in K _p at a given K _aq ; however, there is relatively little decrease in capture zone width when the K _p of freshly installed reactive media is roughly 10 times higher than the K _aq . For a given barrier system, the absolute capture zone width increases with an increase in barrier size, whereas the increment of relative capture zone width decreases dramatically. Although the capture zone width remains relatively unchanged as groundwater flow velocity increases, it results in a shorter residence time in the reactive media that may require greater barrier thickness so that contaminant levels can be reduced to regulatory limits. In addition, the effect of parallel barriers interaction on the capture zone width should be incorporated into the design. The present paper is based on the continuous reactive barrier and homogeneous barrier system. Similar methods can be used to analyse the hydrodynamics of funnel-and-gate system and heterogeneous settings by the appropriate modification.     

响应面法优化阴阳极同时作用电化学法处理染料废水

在自制电化学反应器中,以甲基橙模拟染料废水为处理对象,采用Box-Behnken Design响应面法研究了影响阴阳极同时作用电化学法处理染料废水的因素及其交互作用。实验得出各因素对废水脱色率影响的大小顺序为：电流密度> Fe³⁺浓度>Cl^-浓度。各因素之间的交互作用对废水脱色率影响的大小顺序为：电流密度和Fe³⁺浓度>电流密度和Cl^-浓度>Fe³⁺浓度和Cl^-浓度。优化结果表明：Fe³⁺浓度为1.02 mmol/L、Cl^-浓度为10.96 mmol/L、电流密度为11.52 mA/cm²时,最佳脱色率为94.67%。阴阳极同时作用电化学法对甲基橙去除效果显著。