A／O-化学除磷工艺中DMBR动态膜成膜条件研究

根据动态膜原理，将0．1mm孔径无纺布为膜材的动态膜反应器（Dynamic Membrane BioReactor，DMBR）应用于A／O-化学除磷工艺之中，在动态膜反应器内完成泥水分离。试验测试了曝气强度、初始膜通量和污泥浓度对动态膜成膜的影响。结果表明，曝气强度和初始膜通量是影响成膜的关键性参数。当曝气强度≥60m^3／m^2·h或初始膜通量≥70L／m^2·h，2h内均不能形成截留性能良好的动态膜。在VSS／SS较低的污泥系统中，适宜的成膜条件为：曝气强度≤40m^3／m^2·h；初始膜通量≤40L/m^2·h。     

水解酸化-好氧工艺处理感光材料有机废水研究

感光材料有机生产废水含有多种合成有机物，其BOD5／CODer比值为0．46～0．48，可生化性良好，经水解酸化处理后该废水的BOD5／CODcr的比值可提高至0．54～056，平均增加了17％左右。水解酸化－好氧串联工艺对该废水总的处理效果表明：在废水CODer进水浓度2000～2500mg／L范围内，CODer总去除率可达95％左右，BOD5总去除率可达97％左右；水解酸化后好氧生化系统的动力学半速度常数Ks＝103mg／L，最大比降解速度K＝5．0／日。     

生物除磷机理及试验研究

介绍了生物除磷机理、生物除磷系统的积磷细菌、生物除磷所需的环境条件。SBR法除磷的试验研究表明,应用SBR活性污泥系统进行除磷,需要一定的厌氧条件;且须在厌氧阶段进行充足的曝气。试验结果证明,SBR法在时间上控制的灵活性非常适合生物除磷的环境条件。厌氧与好氧相结合,能够提高磷的去除率或降低出水磷的浓度,磷的去除率可达90%左右。     

强化混凝去除黄浦江水有机物的试验研究

强化混凝去除有机物的效果与水源的分子量分布特性有着密切的关系.由于黄浦江水中低分子量的溶解性有机物占多数,因此,强化混凝处理有机物效果有限.对于＜1k分子量区间的有机物.增加混凝剂投量可有效去除紫外吸光值(UV254),但去除溶解性有机碳(DOC)的效果很差.尽管增加混凝剂投量和降低pH都能有效地去除有机物,但决定强化混凝效果的主要因素是pH,去除黄浦江水有机物的最佳pH范围为6～5.     

微波密封消解法快速测定总磷

对微波密封消解法测定总磷进行了研究．实验结果表明：该法操作简单、消解时间短，准确度高，精密度好，值得普及和推广．     

提高氧化沟法城市污水处理系统除磷效果探讨

根据厦门市集美污水处理厂的实际生产情况,通过对除磷原理的分析,从溶解氧、泥龄、回流及进水方式3个方面出发,在实际生产中进行调控测算,从而找出提高污水处理系统除磷效果的有效方法。     

典型北方高碱度微污染水体强化混凝的示范研究

以高碱度、受有机物污染的典型北方水体为例,探索适宜的强化混凝技术.在水质调查的基础上,提出适合水质特征的强化混凝目标.研究了高碱度水体强化混凝技术方法.研究表明,可以通过3条技术途径提高水体中有机物的去除效率.其一在混凝前优化pH,促进絮凝剂水解形成中聚体,AlCl3在pH 6左右,FeCl3在pH 5左右时,有机物去除率可以提高一倍左右;其二是强化沉淀软化;其三是絮凝剂优化.结合我国实际情况,通过对传统絮凝剂进行改性,研制出了适合我国北方水质特征的高效絮凝剂,能较传统絮凝剂将有机物去除率提高30%以上.     

Simultaneous determination of dissolved organic nitrogen, nitrite, nitrate and ammonia using size exclusion chromatography coupled with nitrogen detector

Accurate quantification of dissolved organic nitrogen (DON) has been a challenge due to the cumulative analytical errors in the conventional method via subtracting dissolved inorganic nitrogen species (DIN) from total dissolved nitrogen (TDN). Size exclusion chromatography coupled with an organic nitrogen detector (SEC-OND) has been developed as a direct method for quantification and characterization of DON. However, the applications of SEC-OND method still subject to poor separations between DON and DIN species and unsatisfied N recoveries of macromolecules. In this study, we packed a series of SEC columns with different lengths and resin materials for separation of different N species and designed an independent vacuum ultraviolet (VUV) oxidation device for complete oxidation converting N species to nitrate. To guarantee sufficient N recoveries, the operation conditions were optimized as oxidation time ≥ 30 min, injection mass (sample concentration × injection volume) < 1000 µL × mg-N/L for macromolecular proteins, and neutral pH mobile eluent. The dissolved O₂ concentration in SEC mobile phase determined the upper limit of VUV oxidation at a specific oxidation time. Compared to conventional HW50S column (20 × 250 mm), HW40S column (20 × 350 mm) with mobile phase comprising of 1.5 g/L Na₂HPO₄·2H₂O + 2.5 g/L KH₂PO₄ (pH = 6.85) could achieve a better separation of DON, nitrite, nitrate, and ammonia. When applied to river water, lake water, wastewater effluent, groundwater, and landfill leachate, the SEC-OND method could quantify DON as well as DIN species accurately and conveniently even the DIN/TDN ratio reached 0.98.     

Insights into reactive oxygen species formation induced by water-soluble organic compounds and transition metals using spectroscopic method

Ambient particulate matter (PM) can cause adverse health effects via their ability to produce Reactive Oxygen Species (ROS). Water-Soluble Organic Compounds (WSOCs), a complex mixture of organic compounds which usually coexist with Transition Metals (TMs) in PM, have been found to contribute to ROS formation. However, the interaction between WSOCs and TMs and its effect on ROS generation are still unknown. In this study, we examined the ROS concentrations of V, Zn, Suwannee River Fulvic Acid (SRFA), Suwannee River Humic Acid (SRHA) and the mixtures of V/Zn and SRFA/SRHA by using a cell-free 2′,7′-Dichlorodihydrofluorescein (DCFH) assay. The results showed that V or Zn synergistically promoted ROS generated by SRFA, but had an antagonistic effect on ROS generated by SRHA. Fluorescence quenching experiments indicated that V and Zn were more prone to form stable complexes with aromatic humic acid-like component (C1) and fulvic acid-like component (C3) in SRFA and SRHA. Results suggested that the underlying mechanism involving the fulvic acid-like component in SRFA more tending to complex with TMs to facilitate ROS generation through π electron transfer. Our work showed that the complexing ability and complexing stability of atmospheric PM organics with metals could significantly affect ROS generation. It is recommended that the research deploying multiple analytical methods to quantify the impact of PM components on public health and environment is needed in the future.     

滇池流域农田氮、磷肥施用现状与评价

2001年6月至9月分别对流域内晋宁，呈贡，西山，官渡和嵩明调查了365家农户有关化肥施用情况，调查分析和计算表明，每年从种植业流失的化肥中纯氮（N）达2575t，纯磷（P）达218t，蔬菜和花卉地的单位面积氮流失量是水田和旱地的7-20倍。菜地年每公顷流失氮204kg，水田的氮流失量最低，平均每公顷每年流失10kg。磷的流失也以蔬菜，花卉地为最高，蔬菜和花卉地的单位面积磷流失量是水田和旱地的9-10倍。研究结果证明，大量的氮，磷化肥施用，通过地表径流和地下水流入滇池是造成其水体富营养化的重要原因之一^[6]，随着农业和农村经济的发展，蔬菜，花卉等经济作物在滇池流域的种植面积将会逐年扩大，因氮，磷化肥的施用面造成的氮，磷流失量将会不断加大，为了实现减少氮，磷化肥对滇池的污染，应积极推广精确施肥，平衡施肥等科学施肥技术，提高化肥利用率，减少化肥流失。增施有机肥，降低化肥用量，同时提高农村居民的环境意识，加强环境管理，依法保护农村环境，控制农业面源污染。