Carrousel氧化沟的三维流场模拟与分析

利用CFD的Fluent软件，采用标准的三维K—ε紊流模型，对桂林市七里店污水处理厂1#氧化沟的流场进行了数值模拟，对导流墙和推进器附近的流速进行了计算分析。结果表明，氧化沟下层流速较低，局部区域流速低于0．2m／s。为了防止污泥沉降，应进一步降低推进器位置。能量损失分析表明，卡罗塞氧化沟能量损失主要来源于沿程摩擦损失和局部损失。可通过增加墙体光滑度、降低入口高度以及增加导流墙的曲率半径等措施减少能量损失，改善现有氧化沟的水力特征。     

Cu-Mn-Zr复合催化剂制备及其催化氧化乙酸乙酯性能

采用溶胶凝胶法制备了4种不同金属摩尔比的Cu-Mn-Zr复合催化剂，利用BET、XRD和XPS对其进行了表征分析，通过固定床管式反应器评价了其对乙酸乙酯模拟气体的催化活性，定性测定了其催化反应降解产物.结果表明，Mn的加入增大了催化剂的比表面积和总孔容，催化剂的N₂吸附-解吸等温线为IV型.Cu-Zr（1：1）催化剂观察到氧化铜晶体和四方晶型氧化锆晶体，氧化铜晶体随着Cu比例的减小而降低，Mn的加入导致氧化锆晶体消失.催化剂无固定形态，呈现良好的分散性.增大Mn/Zr摩尔比能提高催化活性.Cu-Mn-Zr的适当组分比能提高其低温催化活性，其中Cu-Mn-Zr（1：1：1）催化剂的低温催化活性与CO₂的选择性较佳，在200℃时对CO₂的选择性达到96.7%.降解产物分析表明，乙酸乙酯降解中间产物有乙酸和乙醇，最终降解产物主要有CO₂和H₂O等.     

臭氧氧化处理化工污水厂尾水

采用臭氧氧化工艺处理某化工污水厂尾水,考察了臭氧投加量对废水处理效果的影响,并进行了反应动力学研究。实验结果表明,最佳臭氧投加量为67 mg/L,在此条件下,处理后废水的COD去除率为19%,色度去除率为90%,UV254去除率为79%,BOD5/COD为0.11。反应动力学分析结果表明:臭氧氧化去除废水COD的反应适合采用二级反应动力学进行拟合,二级反应动力学方程为y=0.000 1x+0.000 3,相关系数为0.938 5;臭氧氧化去除废水色度的反应更适合采用一级反应动力学进行拟合,一级反应动力学方程为y=0.105 0x-0.018 4,相关系数为0.990 3。     

Soil Zinc contamination from corrosion of galvanized structures

The present work relates to galvanized structures with several years of time life subjected to atmospheric corrosion, like galvanized high tension steel pylons. The mass and fate of zinc released is evaluated both via empirical and experimental procedures. The corrosion rate determination requested atmospheric condition characterization, especially for SO 2 concentration and experimental activities focused on soil sampling around pylons. The soil zinc content, total and exchangeable, is determinates by different analytical procedures. The zinc diffusion in environment and the zinc extension under the top soil is evaluated using 1-dimensional mathematical model for miscible species in porous soil.     

大气污染物等浓度曲线画法初探

介绍一种环境影响评价中大气污染物等浓度曲线的画法，可用于绘制任意接近的等浓度曲线而不会相交或相切，运算量较小且与图形大小无关。     

Photocatalytic Degradation of the Herbicide Erioglaucine in the Presence of Nanosized Titanium Dioxide: Comparison and Modeling of Reaction Kinetics

The present work mainly deals with photocatalytic degradation of a herbicide, erioglaucine, in water in the presence of TiO₂ nanoparticles (Degussa P-25) under ultraviolet (UV) light illumination (30 W). The degradation rate of erioglaucine was not so high when the photolysis was carried out in the absence of TiO₂ and it was negligible in the absence of UV light. We have studied the influence of the basic photocatalytic parameters such as pH of the solution, amount of TiO₂, irradiation time and initial concentration of erioglaucine on the photodegradation efficiency of erioglaucine. A kinetic model is applied for the photocatalytic oxidation by the UV/TiO₂ system. Experimental results indicated that the photocatalytic degradation process could be explained in terms of the Langmuir–Hinshelwood kinetic model. The values of the adsorption equilibrium constant, K, and the second order kinetic rate constant, k, were 0.116 ppm^{? 1} and 0.984 ppm min^{? 1}, respectively. In this work, we also compared the reactivity between the commercial TiO₂ Degussa P-25 and a rutile TiO₂. The photocatalytic activities of both photocatalysts were tested using the herbicide solution. We have noticed that photodegradation efficiency was different between both of them. The higher photoactivity of Degussa P-25 compared to that of rutile TiO₂ for the photodegradation of erioglaucine may be due to higher hydroxyl content, higher surface area, nano-size and crystallinity of the Degussa P-25. Our results also showed that the UV/TiO₂ process with Degussa P-25 as photocatalyst was appropriate as the effective treatment method for removal of erioglaucine from a real wastewater. The electrical energy consumption per order of magnitude for photocatalytic degradation of erioglaucine was lower with Degussa P-25 than in the presence of rutile TiO₂.     

闽江口鳝鱼滩芦苇湿地沉积物甲烷产生与氧化潜力对外源物质输入的响应

研究河口湿地沉积物甲烷(CH4)产生和氧化对外源物质输入的响应,对环境保护及温室气体减排具有重要意义.本研究基于室内培养-气相色谱法,探讨了闽江河口半咸水芦苇(Phragmites australis)沼泽湿地沉积物CH4产生与氧化对不同外源物质(底物、电子受体和营养物质)输入的响应.结果表明:CH3OH(500 mg·kg-1)、C3H9N(500 mg·kg-1)和Fe2+(0~500 mg·kg-1)对CH4产生潜力起促进作用(p0.05);NO-3(0~500 mg·kg-1)、NO-2(0~500 mg·kg-1)、Fe3+(50 mg·kg-1)和NH+4(50~500 mg·kg-1)表现为抑制CH4产生潜力(p0.05);而0~50 mg·kg-1的CH3OH和C3H9N、0~500 mg·kg-1的CH3COOH、SO2-4、Mn4+、PO3-4和低剂量的NH+4(0~5 mg·kg-1)对CH4产生的影响不显著(p0.05).实验剂量内(0~500 mg·kg-1),Fe3+和Mn4+的添加可促进CH4氧化(p0.05);CH3COOH、CH3OH、C3H9N、NO-3、NO-2、SO2-4、NH+4和低剂量的PO3-4(0~50 mg·kg-1)对沉积物CH4氧化潜力均有显著的抑制作用(p0.05);而Fe2+对CH4氧化没有显著影响(p0.05).综合分析表明,CH3COOH、CH3OH、C3H9N、NO-3、NO-2、SO2-4、PO3-4、NH+4和Fe2+的输入对沉积物CH4产生和氧化的综合作用为增加CH4排放通量,而Fe3+和Mn4+输入的综合作用则与之相反.     

饮用水中卡马西平的臭氧和二氧化氯降解研究

采用臭氧(O3)和二氧化氯(ClO2)2种消毒方式对饮用水中卡马西平(CBZ)进行氧化降解,考察了不同影响因素(pH值、温度)条件下的氧化动力学,并通过对CBZ降解副产物的确定推测了2种消毒条件下CBZ的降解途径.结果表明,序批式条件下O3和ClO2对CBZ的降解均遵循二级反应动力学.pH值的升高对CBZ的O3和ClO2降解有负面效果;在10 ～ 25℃范围内,温度对CBZ的O3降解速率常数影响较小,但CBZ的ClO2降解速率常数随温度升高显著升高.采用UPLC-Q-TOF-MS对CBZ的O3和ClO2降解前后样品溶液进行扫描,均检测到8种降解中间产物,2种氧化方式主要通过环化加成、亲电取代(羟基化和氯取代)及杂环上的重排等途径来实现对CBZ结构的破坏.     

FISH-NanoSIMS技术在环境微生物生态学上的应用研究

微生物分子生态学技术的不断发展,使得同时分析复杂生态系统中微生物的分布和功能特征成为可能.为了研究荧光原位杂交-纳米二次离子质谱技术(fluorescence in situ hybridization-Nano secondary ion mass spectroscopy,FISH-Nano SIMS)在环境微生物生态学上的应用,本研究采用稳定同位素标记的化合物13C-C6H12O6、15N-NH4Cl作为C源和N源,分别对纯培养锰氧化细菌假单胞菌Pseudomonas sp.QJX-1(培养基加锰及不加锰两种条件下),以及浅层土壤及厌氧污泥两种环境样品进行培养.利用FISH-NanoSIMS技术检测培养后样品中微生物体内12C-、13C-、12C14N-、12C15N-的分布特征及其丰度值,进而探讨纯菌及环境样品中微生物利用同位素碳氮源的情况.结果显示所有样品细菌分布区域对应的同位素碳氮(13C、15N)的含量均显著大于其自然丰度值,这表明Pseudomonas sp.QJX-1及环境样品中的微生物均能代谢13C-C6H12O6和15N-NH4Cl.研究进一步发现,Pseudomonas sp.QJX-1在碳氮源消耗至较低浓度时才进行锰氧化;浅层土壤和厌氧污泥中可能都存在同步硝化反硝化细菌群落.FISH和Nano SIMS技术联用能同时分析环境样品中特定微生物的分布特征及代谢功能,进而能更好地掌握环境样品中微生物群落的生理生态学特征.