应用悬浮填料预处理微污染原水的影响因素探讨

对采用悬浮填料的生物接触氧化原水预处理技术的影响因素进行了探讨。分析了自然挂膜条件下的工艺启动过程，研究了停留时间、气水比、温度、浊度条件对污染物去除效果的影响。通过夏、秋、冬季的中试运行效果表明：停留时间为60min，生物预处理装置对污染物的去除具有较好的效果；温度低于8.5℃，对氨氮去除效果影响较大；浊度对本工艺运行影响不大；气水比为0.375，足够满足生物预处理的运行。     

悬浮填料生物反应器处理低浓度氨氮的动力学特性分析

城市污水经一级强化处理后,NH3-N浓度为10~15mg/L,CODCr为40~60mg/L。试验利用悬浮填料床对一级强化处理出水中的氨氮进行深度处理,分析了悬浮填料表面负荷和硝化速率与水力停留时间的关系,并模拟分析了硝化速率与氨氮浓度的关系。结果表明,悬浮填料床内混合液氨氮浓度为0.5~2.5mg/L时,硝化反应符合半级反应动力学,半级反应速率常数k1/2为0.48(g/m)0.5/d;混合液氨氮浓度>2.1mg/L时,硝化反应遵循零级反应动力学,rmax为0.71g/(m2.d)。动力学理论计算值与实际运行结果基本吻合,说明动力学模型对悬浮填料床的硝化性能具有良好的预测和指导意义。     

自动控制实现两级混合床反应器处理垃圾渗滤液的短程硝化

采用两级混合床反应器(分别命名为 Hybrid Ⅰ和 HybridⅡ).对垃圾渗滤液中的COD和氨氮去除进行了试验研究,混合床由颗粒悬浮载体和固定组合软性填料相结合.试验以反应器的 DO、pH、ORP、SS等作为在线控制参数,研究了该反应器在固定温度(28～33℃)、不同进水负荷、DO 和 pH值下的运行效果,最后在 Hybrid 反应器的优化控制条件(DOHrbrid Ⅰ=(2.0±0.2)mg·L-1,DOHbrid Ⅱ=(1.5±0.2)mg·L-1,pHHybrid Ⅰ=8.0±0.2,pHHybrid Ⅱ=8.5±0.2,周期进水量为50L)下,实现了COD的高效去除以及氨氮的短程硝化去除.垃圾渗滤液进水 COD和氨氮分别为2300～5700mg·L-1和580～1150mg·L-1.两级混合床反应器工艺的COD和氨氮的去除率分别为93%和95%左右,总氮(TN)的去除率在82%以上.连续运行过程中 Hybrid Ⅰ和 Hybrid Ⅱ反应器的COD最大去除速率分别为 1.91 kg·m-3·d-1和0.75kg·m-3·d-1,氨氮亚硝化速率最大分别为 0.54kg·m-3·d-1和0.33kg·m-3·d-1.运行结果表明,该工艺耐冲击负荷强,处理效果稳定.     

全程自养脱氮工艺的研究

以悬浮填料床作为全程自养脱氮反应器，用不含有机碳的合成氨氮废水进行反应器的启动。系统的氨氮和总氮去除率分别达80％和60％左右。通过批式实验对全程自脱氮做进一步的研究。结果表明，通过控制反应器中DO的浓度，可以控制氨氧化和反硝化的比率；当DO为0.8mg/L时，氨氮几乎完全转化为氮气，氨氧化和反硝化在此时达到了动态平衡；在低DO情况下，氨氮和亚硝氮同时存在，氨氮和总氮的转化率都大幅度的提高，说明氨氮可以亚硝氮为电子受体，在无外加有机碳源的情况下进行反硝化。     

反硝化悬浮填料适用性及其微生物群落结构解析

为研究温度及处理负荷对缺氧挂膜悬浮填料的活性恢复效果的影响,将填料分别置于低负荷、冲击负荷和低温环境中进行活性恢复适用性实验.结果表明在填料活性恢复过程中起关键作用的是EPS中多糖的增加,冲击负荷和低温条件下多糖含量增加比蛋白质更为明显.而低负荷下多糖和蛋白质含量均高于另外两者.缺氧挂膜悬浮填料的活性恢复对冲击负荷条件的适用性较好,低温条件次之,对低负荷环境适用性较差.另外,低负荷、冲击负荷和低温环境中Proteobacteria菌门的相对丰度分别由15 d时的72.23%、78.66%和76.35%上升至25d时的83.17%、84.30%和80.46%,15 d时低负荷下Proteobacteria菌相对丰度低于其他反应器,缺氧悬浮填料不能作为污水处理厂低负荷下总氮快速达标的备选方案.反硝化功能菌属Dechloromonas相对丰度的增加可能是引起填料生物膜反硝化脱氮能力提高的重要原因.Flavobacterium菌属的存在可能促进了低温下填料生物膜反硝化脱氮能力的恢复.不同恢复环境对缺氧生物膜恢复完成时的生物多样性影响较小.     

温度对生物炭滤池处理高氨氮原水硝化的影响

利用臭氧预氧化-生物预处理-混凝沉淀-砂滤-臭氧后氧化-生物活性炭滤池组合工艺对微污染水源水进行了深度处理中间试验.将一部分未经生物预处理的高氨氮原水经常规处理后进入生物活性炭滤池以提高活性炭滤池进水氨氮浓度.研究了温度对高氨氮进水条件下生物活性炭滤池硝化能力的影响.试验表明,生物活性炭(BAC)的生物活性随温度的降低而降低.在水温2℃左右时,生物活性炭滤池对氨氮的去除能力相当于6℃以上时去除能力的50%;在温度>6℃的条件下,生物活性炭滤池对氨氮的去除能力在进水溶解氧基本相同时不随温度(水温>6℃)的变化而发生变化,对氨氮的去除能力主要受水中溶解氧的影响.     

短程硝化反硝化新型生物反应器的特性研究

利用气提式反应器研究硝化过程中的亚硝酸积累现象,并在运行6个月后将其与一升流式污泥床反应器相连接,研究硝化反硝化联合工艺的处理效果。结果表明,在硝化部分,当进水氨氮浓度>98mg/L,游离氨(FA)为1.07mg/L时,亚硝态氮浓度开始逐渐上升,亚硝化率(NO2--N/NOX--N)>50%。实验条件下氨氮污泥负荷为0.53kg/(kg·d)时,氨氮去除率较高且亚硝化率最大,但当污泥负荷达到0.85kg/(kg·d)时,氨氮去除率降低。升流式污泥床反应器中形成明显的颗粒污泥,在碳源充足的条件下(即C/N>3),最终出水效果显著提高。     

移动床生物膜反应器处理废水的特性研究

以氧吸收速率(Rou)为指标,研究了移动床生物膜反应器内两相污泥中自养菌和异养菌的生物活性.分别测定了不同温度和不同负荷下,反应区内悬浮相和附着相污泥的Rou.结果表明:温度为5 ℃时,自养菌的硝化活性为18 ℃时的60%左右;附着相微生物的硝化能力较悬浮相微生物低20%～30%;该反应器具有良好的抗低温和负荷冲击的能力.该反应器内2个反应区中附着相和悬浮相污泥的生物活性为:反应区Ⅱ悬浮相>反应区Ⅰ悬浮相>反应区Ⅱ附着相>反应区Ⅰ附着相.反应区Ⅰ,Ⅱ的反硝化速率分别为0.44和0.63 mg/(g·h),说明后者污泥的反硝化活性好于前者.试验结果还表明,在反应器内NO2--N的积累量非常低.      

较高负荷条件下活性污泥-生物膜联合系统对氮磷的去除

中试试验条件下,考察了较高的有机负荷对活性污泥-悬浮载体生物膜联合系统对氮磷去除效果的影响。试验表明,水温为20~33℃时,在联合系统污泥龄为4~9d,有机负荷达到0.18~0.55kg/kg.d条件下,对磷的去除效果稳定在90%左右,氨氮的去除率达到80%以上,出水总氮平均为11mg/L,达到《城镇污水处理厂污染物排放标准》(GB18918-2002)中一级排放标准。同时,试验过程中也发现了联合系统的好氧池中存在明显的同步硝化反硝化现象,并初步分析了其原因与影响因素。     

全程自养脱氨氮悬浮填料床反应器性能的研究

以NH+4-N溶液为基质建立和启运了全程自养脱氨氮悬浮填料床反应器,反应器连续运行的实验结果表明在pH为8.0～8.5、溶解氧为0.7～1.0mg/L和温度为28℃的条件下.当氨氮表面负荷为2～2.5g/(m2@d)时,其表面去除速率为1.1～1.3/(m2@d),全程自养脱氮率基本稳定在55%左右;全程自养脱氮的最适pH范围为7.5～8,5,其中最佳pH为8.0左右;最适溶解氧范围为0.5～1.5mg/L,其中尤以0.8～1.0ms/L左右为最佳.     

Toxic effects of acetochlor, methamidophos and their combination on nifH gene in soil

Toxic effects of two agrochemicals on nifH gene in agricultural black soil were investigated using denaturing gradient gel electrophoresis （DGGE） and sequencing approaches in a microcosm experiment. Changes of soil nifH gene diversity and composition were examined following the application of acetochlor, methamidophos and their combination. Acetochlor reduced the nifH gene diversity （both in gene richness and diversity index values） and caused changes in the nifH gene composition. The effects of acetochlor on nifH gene were strengthened as the concentration of acetochlor increased. Cluster analysis of DGGE banding patterns showed that nifH gene composition which had been affected by low concentration of acetochlor （50 mg/kg） recovered firstly. Methamidophos reduced nifH gene richness that except at 4 weeks. The medium concentration of methamidophos （150 mg/kg） caused the most apparent changes in nifH gene diversity at the first week while the high concentration of methamidophos （250 mg/kg） produced prominent effects on nifH gene diversity in the following weeks. Cluster analysis showed that minimal changes of nifH gene composition were found at 1 week and maximal changes at 4 weeks. Toxic effects of acetochlor and methamidophos combination on nifH gene were also apparent. Different nifH genes （bands） responded differently to the impact of agrochemicals： four individual bands were eliminated by the application of the agrochemicals, five bands became predominant by the stimulation of the agrochemicals, and four bands showed strong resistance to the influence of the agrochemicals. Fifteen prominent bands were partially sequenced, yielding 15 different nifH sequences, which were used for phylogenetic reconstructions. All sequences were affiliated with the alpha- and beta-proteobacteria, showing higher similarity to eight different diazotrophic genera.     

EDTA-enhanced phytoremediation of lead contaminated soil by Bidens maximowicziana

Phytoremediation is a potential cleanup technology for the removal of heavy metals from contaminated soils.Bidens maximowicziana is a new Pb hyperaccumulator,which not only has remarkable tolerance to Pb but also extraordinary accumulation capacity for Pb.The maximum Pb concentration was 1509.3 mg/kg in roots and 2164.7 mg/kg in overground tissues.The Pb distribution order in the B. maximowicziana was:leaf>stem>root.The effect of amendments on phytoremediation was also studied.The mobility of soil Pb and the Pb concentrations in plants were both increased by EDTA application.Compared with CK(control check),EDTA application promoted translocation of Pb to overground parts of the plant.The Pb concentrations in overground parts of plants was increased from 24.23-680.56 mg/kg to 29.07-1905.57 mg/kg.This research demonstrated that B.maximowicziana appeared to be suitable for phytoremediation of Pb contaminated soil,especially,combination with EDTA.     

Distribution and ecological effect of mercury in Laogang landfill, Shanghai, China

Laogang landfill near Shanghai is the largest landfill in China, and receives about 10000 t of daily garbage per day, Samples of topsoil and plants were analyzed to evaluate mercury pollution from the landfill. For topsoil samples, there were significant correlations among total mercury （HgT）, combinative mercury （Hgc） and gaseous mercury （HgG）, and content of total organic carbon （TOC）, but, no significantly relationship was found between Hg content and filling time. Hg content changes in vertical profiles with time showed that the average Hgv of profiles 1992, 1996, and 2000 was similar, but their average HgG was quite different. HgT was significantly correlated with Hgc in profile 1992 and 2000, and Hgv was significantly correlated with Hg6 in profile 1996. HgG/Hgv ratio in profile samples decreased in the order of （HgG,/HgT）1992〉（HgG/HgT）1996〉〉（HgG/HgT）2000. A simple outline of Hg release in landfill could be drawn： with increasing of filling time, degradation undergoes different biodegradation, accordingly, gaseous mercury goes through small, more, and small proportion to total mercury. Distribution of Hg in plants was inhomogeneous, following the order of leaf〉root〉stem. The highest value of leaf may be associated with higher atmospheric Hg from landfill. Ligneous plants （e.g. Phyllostachys glanca, Prunus salicina and Ligustrum lucidum） are capable of enriching more Hg than herbaceous plants.     

Arsenic uptake by arbuscular mycorrhizal maize （Zea mays L.） grown in an arsenic-contaminated soil with added phosphorus

The effects of arbuscular mycorrhizal (AM) fungus (Glomus mosseae) and phosphorus (P) addition (100 mg/kg soil) on arsenic (As) uptake by maize plants (Zea mays L.) from an As-contaminated soil were examined in a glasshouse experiment.Non-mycorrhizal and zero-P addition controls were included.Plant biomass and concentrations and uptake of As,P,and other nutrients,AM colonization,root lengths,and hyphal length densities were determined.The results indicated that addition of P significantly inhibited root colonization and development of extraradical mycelium.Root length and dry weight both increased markedly with mycorrhizal colonization under the zero-P treatments,but shoot and root biomass of AM plants was depressed by P application.AM fungal inoculation decreased shoot As concentrations when no P was added,and shoot and root As concentrations of AM plants increased 2.6 and 1.4 times with P addition,respectively.Shoot and root uptake of P,Mn,Cu,and Zn increased,but shoot Fe uptake decreased by 44.6%,with inoculation, when P was added.P addition reduced shoot P,Fe,Mn,Cu,and Zn uptake of AM plants,but increased root Fe and Mn uptake of the nonmycorrhizal ones.AM colonization therefore appeared to enhance plant tolerance to As in low P soil,and have some potential for the phytostabilization of As-contaminated soil,however,P application may introduce additional environmental risk by increasing soil As mobility.     

Enzymatic oxidation of aqueous pentachlorophenol

The influence of the nonionic surfactant Tween 80 on pentachlorophenol （PCP） oxidation catalyzed by horseradish peroxidase was studied. The surfactant was tested at concentrations below and above its critical micelle concentration （CMC）. Enhancement of PCP removal was observed at sub-CMCs. The presence of Tween 80 in the reaction mixture reduced enzyme inactivation which occurred through a combination of free radical attack and sorption by precipitated products. A simple first-order model was able to simulate time profiles for enzyme inactivation in the presence or absence of Tween 80. At supra-CMCs, the surfactant caused noticeable reductions in PCP removal, presumably through micelle partitioning of PCP which precluded the hydrophobic PCP molecule from interacting with the enzyme.     

Decomposition of alachlor by ozonation and its mechanism

Decomposition and corresponding mechanism of alachlor, an endocrine disruptor in water by ozonation were investigated. Results showed that alachlor could not be completely mineralized by ozone alone. Many intermediates and final products were formed during the process, including aromatic compounds, aliphatic carboxylic acids, and inorganic ions. In evoluting these products, some of them with weak polarity were qualitatively identified by GC-MS. The information of inorganic ions suggested that the dechlorination was the first and the fastest step in the ozonation of alachlor.     

Degradation of metabolites accumulated of benzo[a]pyrene by coupling Penicillium Chrysogenum with KMnO4

Several main metabolites of benzo[a]pyrene （BaP） formed by Penicillium chrysogenum, Benzo[a]pyrene-1,6-quinone （BP 1,6- quinone）, trans-7,8-dihydroxy-7,8-dihydrobenzo[a]pyrene （BP 7,8-diol）, 3-hydroxybenzo[a]pyrene （3-OHBP）, were identified by high-performance liquid chromatography （HPLC）. The three metabolites were liable to be accumulated and were hardly further metabolized because of their toxicity to microorganisms. However, their further degradation was essential for the complete degradation of BaP. To enhance their degradation, two methods, degradation by coupling Penicillium chrysogenum with KMnO4 and degradation only by Penicillium chrysogenum, were compared; Meanwhile, the parameters of degradation in the superior method were optimized. The results showed that （1） the method of coupling Penicillium chrysogenum with KMnO4 was better and was the first method to be used in the degradation of BaP and its metabolites; （2） the metabolite, BP 1,6-quinone was the most liable to be accumulated in pure cultures; （3） the effect of degradation was the best when the concentration of KMnO4 in the cultures was 0.01% （w/v）, concentration of the three compounds was 5 mg/L and pH was 6.2. Based on the experimental results, a novel concept with regard to the bioremediation of BaP-contaminated environment was discussed, considering the influence on environmental toxicity of the accumulated metabolites.     

Impact of atrazine and nitrogen fertilizers on the sorption of chlorotoluron in soil and model sorbents

Sorption of chlorotoluron in ammonium sulfate, urea and atrazine multi-solutes system was investigated by batch experiments. The results showed application of nitrogen fertilizers to the soil could affect the behavior of chlorotoluron. At the same concentration of N, sorption of chlorotoluron decreased as the concentration of atrazine increased on the day 0 and 6 in soil, respectively. The sorption of chlorotoluron increased from 0 to 6 d when soils were preincubated with deionized water, ammonium sulfate and urea solution for 6 d. That indicated incubation time was one of the most important factors for the sorption of chlorotoluron in nitrogen fertilizers treatments. The individual sorption isotherms of chlorotoluron in rubbery polymer and silica were strictly linear in single solute system, but there were competition sorption between pesticides or between pesticides and nitrogen fertilizers. That indicated the sorption taken place by concurrent solid-phase dissolution mechanism and sorption on the interface of water-organic matter or water-mineral matter.     

基于综合水质标识指数和对应分析法的校园河道水质评价

以三峡大学的校园河道求索溪为研究对象,利用综合水质标识指数法确定求索溪水质类别,分析其水质时空变化规律,并利用对应分析法得出求索溪中不同监测点的主要污染因子.研究结果表明:求索溪整体的综合水质标识指数为7.423,整体水质为劣V类(地表水环境质量标准GB 3838-2002)且黑臭.从时间变化来看,求索溪4月份的水质最差,5月份次之,4、5月份所有监测点的水质都劣于V类且黑臭;8月份水质最好,水质为Ⅳ类;从空间分布来看,8个监测点综合水质标识指数均超过6.0,水质为劣V类,其中6号监测点的水质相对最好,监测点3号的水质相对最差;对应分析法得出求索溪的整体水体污染程度受总氮因子的影响最大,其次为总磷.该研究拟为求索溪及类似校园河道的水环境治理研究提供基础依据和参考.     

Potential of plant polyphenol oxidases in the decolorization and removal of textile and non-textile dyes

In this study an effort has been made to use plant polyphenol oxidases; potato （Solanum tuberosum） and brinjal （Solanum melongena）, for the treatment of various important dyes used in textile and other industries. The ammonium sulphate fractionated enzyme preparations were used to treat a number of dyes under various experimental conditions. Majority of the treated dyes were maximally decolorized at pH 3.0. Some of the dyes were quickly decolorized whereas others were marginally decolorized. The initial first hour was sufficient for the maximum decolorization of dyes. The rate of decolorization was quite slow on long treatment of dyes. Enhancement in the dye decolorization was noticed on increasing the concentration of enzymes. The complex mixtures of dyes were treated with both preparations of polyphenol oxidases in the buffers of varying pH values. Potato polyphenol oxidase was significantly more effective in decolorizing the dyes to higher extent as compared to the enzyme obtained from brinjal polyphenol oxidase. Decolorization of dyes and their mixtures, followed by the formation of an insoluble precipitate, which could be easily removed simply by centrifugation.