含中间层的DSA电极电催化氧化硝基苯废水的研究

为了提高难降解有机废水的可生化性，以及更高效地去除废水中的特征污染物，同时避免二次污染，利用自制的含锡锑中间层的钌钯氧化物涂层电极对有机废水中的硝基苯进行处理，并利用SEM、XRD等方法对电极中间层、表层进行微观表征。微观测试表明，基体、中间层、表层之间结合力较强，有利于增强电极寿命；水处理实验表明，电催化氧化反应体系适合高浓度有机废水的处理，由于该反应体系需要外加电解质加强传质，这在实际运用中为废水中盐度的处理提供了一种新的途径，当电流密度为20 mA/cm²、电解质浓度为10 g/L、pH=5、极板间距=2 cm时，电催化氧化体系对硝基苯具有较高的去除效率。     

脉冲电晕反应器结构对乙硫醇消除效果的影响

研究了脉冲电晕等离子体反应器结构的变化对乙硫醇消除效果的影响规律。结果表明，在反应器内设置折流板，可以增加气流的湍动程度，有利于活性粒子与污染物的充分接触，从而提高消除率。高压电极间距对电晕区范围及消毒效果有较大影响，间距较小将导致各电极产生的电场相互干扰明显，消除率减小；而电极间距过大，虽然电极间电场分布相互干扰小，但是反应器内可排布的电极数减少，总电晕区减少，消除率也减小。根据实验结果，电极间距设置为50 mm比较合理。另外，在相同的电场强度和脉冲频率下，毛刺形高压电极比线电极结构能耗低，能量利用率高。     

TiO2/凹凸棒土复合催化剂的制备及光催化降解活性大红

以凹凸棒土作为载体,以 TiOSO4为钛源,采用超声分散-再沉淀法制备了 TiO2粒径为 10 nm 左右的锐钛矿型 TiO2/凹凸棒土复合催化剂.并采用 X 射线衍射仪、透射电子显微镜、X 射线能谱仪对复合催化剂进行了表征.制备复合催化剂的最佳条件:凹凸棒土与 TiO2的质量比为 1:3.0,煅烧温度为 450 ℃....     

间歇运行式生物滴滤池处理油漆废气中试研究

为研究间歇运行式生物滴滤池对油漆生产厂废气净化能力，建立一座中试规模生物滴滤池（BTF），接种降解菌群，采用8 h/d运行方式净化某油漆厂包装车间废气，并用PCR-DGGE技术揭示BTF细菌群落结构与工艺运行条件间的联系。油漆厂包装车间废气中挥发性有机物（VOCs）主要为甲苯、乙苯、混合二甲苯（间、对和邻二甲苯），BTF对甲苯、乙苯、混合二甲苯最大去除率分别为88.8%、83.7%和86.3%。DGGE分析显示，BTF稳定运行时，主要优势菌相对丰度较为稳定（F，P>0.05），其细菌多样性显著低于启动期（F，P>0.05）；同时，下层填料细菌多样性高于上层填料，其细菌结构变化也较上层明显；另外，提升培养液浓度至2倍和4倍对菌群结构亦无显著影响。     

改良型AO法组合工艺中有机物的三维荧光分析

采用三维荧光(EEM)光谱技术,对上海竹园第二污水处理厂改良型AO法组合工艺运行过程中的各种溶解性有机物(DOM)进行分析,并对比研究传统好氧活性污泥法曝气池出水和A/O脱氮工艺硝化池出水DOM的EEM光谱的迁移变化特性.结果表明,各种DOM中主要的荧光物质有类蛋白质(荧光峰A和B)及类腐殖质(荧光峰C),经改良型AO法组合工艺处理后,荧光峰的强度降低了14％～60％,同时类蛋白质和腐殖质的结构也发生了变化；腐殖酸溯源表明DOM中的腐殖酸以微生物代谢产生的带有荧光基团的腐殖酸类为主.     

质子化壳聚糖的除磷性能

壳聚糖是一类无毒无害的天然高分子絮凝剂,为了提高壳聚糖在污水处理中的除磷性能,采用硫酸溶液对壳聚糖进行质子化改性;考察了质子化度(硫酸溶液pH值)、吸附时间以及原水pH值对除磷效率的影响。研究结果表明,质子化度越大,总磷去除效率越高;在吸附时间为40～50 min的范围内,总磷去除率最大;原水pH值对质子化壳聚糖的总磷去除效率有明显影响,在质子化度较低时(硫酸溶液pH值≥3),随着原水pH值的增加,总磷去除率降低,在质子化度较高时(硫酸溶液pH值=2),在原水pH=6时,总磷去除率最大;质子化壳聚糖的吸附过程较好地遵循Lagergren准二级动力学模型和Langmuir吸附等温方程,吸附热力学参数ΔH<0,ΔG<0,ΔS<0,吸附过程表现为放热、自发的单分子层化学吸附过程。     

水位波动带氮素迁移转化规律

为考察水位波动对非饱和-饱和土层中氮素迁移转化的影响，设计土柱实验装置Ⅰ和Ⅱ分别模拟水位稳定与波动两种情景，测定一个水位波动周期内地下水中NO₃^--N、NO₂^--N和NH₄⁺-N浓度变化情况。结果表明，柱Ⅱ水位第1次下降柱内1^#，2^#，3^#，4^#采样点NO₃^--N浓度均增大，增幅分别为6.5%、14.9%、15.33%和19.8%。水位上升时结果相反，分别降低17.3%、26.15%、50.29%和44.61%。第2次水位下降至初始位置4个采样点NO₃^--N浓度再次增大，幅度分别为7.1%、10.6%、13.89%和7.76%。铵态氮呈相反趋势不同程度的变化。水位波动柱Ⅱ连通水槽内总氮量增加显著高于柱I水槽，即水位波动有利于波动带地下水中氮素垂向迁移，加重波动带以下地下水硝酸盐污染。因此，水位波动对氮素迁移转化的影响不容忽视。     

安全燃放烟花

<正>重要提示:A、严禁携带鞭炮烟花乘坐车、船、飞机等交通工具;B、燃放鞭炮烟花应完全遵守当地政府的规定;C、儿童必须在大人的指导下燃放;D、燃放时一定要选择室外,空旷的环境。     

The structure of the fire fighting foam surfactant Forafac®1157 and its biological and photolytic transformation products

For several decades, perfluorooctane sulfonate (PFOS) has widely been used as a fluorinated surfactant in aqueous film forming foams used as hydrocarbon fuel fire extinguishers. Due to concerns regarding its environmental persistence and toxicological effects, PFOS has recently been replaced by novel fluorinated surfactants such as Forafac®1157, developed by the DuPont company. The major component of Forafac®1157 is a 6:2 fluorotelomer sulfonamide alkylbetaine (6:2 FTAB), and a link between the trade name and the exact chemical structure is presented here to the scientific community for the first time. In the present work, the structure of the 6:2 FTAB was elucidated by ¹H, ¹³C and ¹⁹F nuclear magnetic resonance spectroscopy and high-resolution mass spectrometry. Moreover, its major metabolites from blue mussel (Mytilus edulis) and turbot (Scophthalmus maximus) and its photolytic transformation products were identified. Contrary to what has earlier been observed for PFOS, the 6:2 FTAB was extensively metabolized by blue mussel and turbot exposed to Forafac®1157. The major metabolite was a deacetylated betaine species, from which mono- and di-demethylated metabolites also were formed. Another abundant metabolite was the 6:2 fluorotelomer sulfonamide. In another experiment, Forafac®1157 was subjected to UV-light induced photolysis. The experimental conditions aimed to simulate Arctic conditions and the deacetylated species was again the primary transformation product of 6:2 FTAB. A 6:2 fluorotelomer sulfonamide was also formed along with a non-identified transformation product. The environmental presence of most of the metabolites and transformation products was qualitatively demonstrated by analysis of soil samples taken in close proximity to an airport fire training facility.     

Evidence for the inhibitory effects of silver nanoparticles on the activities of soil exoenzymes

Silver nanoparticles (AgNPs) are well known to have antimicrobial ability, but very little is known about the effect of AgNPs on soil exoenzyme activities, which reflect the potential of a soil to support biochemical processes. This study provides evidence of the inhibitory effects of AgNPs on the activities of soil exoenzymes. Six exoenzymes related to nutrient cycles (urease, acid phosphatase, arylsulfatase, β-glucosidase) and the overall microbial activity (dehydrogenase, fluorescein diacetate hydrolase) were tested in soils treated with AgNPs (1, 10, 100 and 1000 μg g(-1)) and silver ion (0.035, 0.175, 0.525, 1 and 1.5 μg g(-1)). AgNPs were capable of inhibiting the activities of all the exoenzymes tested in this study. Especially, the urease and dehydrogenase activities were significantly related to the presence of AgNPs. The effects of silver ions dissolved from the AgNPs were not significant, indicating the adverse effects caused by AgNPs themselves. This study suggested that AgNPs negatively affect soil exoenzyme activities, with the urease activity especially sensitive to AgNPs.