生物反应器填埋场系统中城市生活垃圾原位脱氮研究

采用填埋垃圾上层间歇曝气充氧或渗滤液回流前经好氧、硝化反应器处理的方式,营造生物反应器填埋场系统内生物脱氮环境,研究了其中生活垃圾原位脱氮的性能.结果表明,在填埋垃圾稳定化过程中,88%以上的含氮化合物以渗滤液的形式溶出.填埋垃圾上层间歇曝气充氧或渗滤液经好氧、硝化反应器处理后回流的生物反应器填埋场系统对渗滤液总氮的处理效果较好,实验结束时,渗滤液总氮量仅为对照填埋场的28.7%和14.3%.     

厌氧-准好氧运行加速生物反应器填埋场垃圾稳定的研究

通过厌氧型、好氧型和准好氧型生物反应器填埋场的比较,提出了厌氧-准好氧联合运行加速生物反应器填埋场垃圾降解和稳定的填埋场运行方法,并通过模拟试验进行了研究.结果表明,按厌氧方式运行710 d的模拟垃圾柱改为按准好氧方式运行360 d后,每天回灌1次的D1柱和每周回灌2次的D4柱渗滤液COD浓度分别由705 mg/L和669 mg/L下降到135mg/L和178 mg/L,氨氮浓度由650 mg/L和877 mg/L降到不能检出水平;而继续按厌氧方式运行的垃圾柱D2和D3的渗滤液COD浓度仅分别由435mg/L和852 mg/L下降到295 mg/L和596 mg/L,氨氮浓度由654 mg/L和1 107 mg/L下降到469mg/L和783 mg/L.模拟厌氧型生物反应器填埋场垃圾柱稳定后期改为按准好氧方式运行,能加快渗滤液COD和氨氮浓度的衰减速率,而较高的渗滤液回灌频率更能强化这一优势.     

回灌型准好氧填埋场脱氮特性及加速稳定化研究

采用2个模拟填埋生物反应器,1号柱渗滤液简单回灌,2号柱为渗滤液回灌准好氧联合运行方式,研究了渗滤液回灌准好氧生物反应器填埋场的脱氮特性及加速垃圾稳定化特性。研究结果表明：渗滤液回灌准好氧填埋场具有很强的脱氮能力,2号柱由厌氧运行方式改为准好氧条件下,渗滤液中的氨氮和凯式氮浓度分别由最大值的3198mg／L和3345mg／L降低到第160d的73mg／L和81mg／L,去除率分别为97．7％和97．6％,pH快速升高到8．0左右,COD浓度快速降低。渗滤液中溶解性有机物（DOM）分级结果表明,2号柱HA和FA含量的增加明显快于1号柱。2号柱DOM的三维荧光光谱特性发生了较大变化,荧光基团从60d结构简单的类蛋白物质转变为95d结构复杂的类胡敏酸和富里酸物质,而1号柱渗滤液DOM荧光基团一直是结构简单的类蛋白物质。结果表明回灌准好氧生物反应器填埋场的稳定化速度远快于简单回灌的生物反应器填埋场。     

模拟新型联合生物反应器填埋场产气速率规律的研究

为了有效利用和管理生物反应器填埋场的填埋气体,减少其稳定过程中温室气体的排放,将厌氧型生物反应器填埋场和准好氧矿化垃圾生物反应床相结合,探索了厌氧-准好氧联合型生物反应器填埋场中厌氧生物反应器填埋场单元的产气规律。研究表明：在产酸阶段,ANBL单元的产气速率在填埋2d后快速达到峰值（1#ANBL为188L/d,2号ANBL为192L/d,3号ANBL为216L/d）,随后迅速下降,并稳定在0-12L/d之间,其变化主要受外界温度和回灌频率的影响。     

生物反应器填埋技术及其应用

本文分析了城市生活垃圾的厌氧、好氧及准好氧填埋方式的特点,介绍了当前国内外垃圾渗滤水场内循环处理的两种趋势:(1)以欧美国家为主的生物反应器填埋技术;(2)以日本为主的循环式准好氧填埋技术。根据我国城市垃圾有机物含量高的特点,提出了将准好氧填埋技术与生物反应器填埋技术特点相结合的垃圾渗滤液场内循环处理的设计思路。     

回灌频率对联合型生物反应器填埋场的影响研究

为解决厌氧型生物反应器填埋场中氨氮积累问题,加速填埋场的稳定化进程,将厌氧生物反应器填埋场和准好氧矿化垃圾反应床串联。实验设置了1个厌氧型生物反应器填埋场(ANBL1#)作为参照组,2个厌氧-准好氧联合型生物反应器填埋场(AN-SABL2#、AN-SABL 3#)作为对照组,以研究不同回灌频率下AN-SABL的稳定化规律。研究结果表明:AN-SABL2#、AN-SABL3#可缩短酸化时间,渗滤液的pH值分别在94周、98周升至大于7,而ANBL1#渗滤液的pH值直至100周仍小于7。AN-SABL系统可有效降解渗滤液COD浓度,实验进行到100周左右时,AN-SABL2#、AN-SABL3#系统中厌氧柱D2、D3柱COD浓度仅为ANBL1#系统中厌氧柱D1柱的40.63%、12.5%,而准好氧柱对渗滤液COD的去除率大部分在95%以上。AN-SABL系统能缓解厌氧型生物反应器填埋场中氨氮积累问题,这主要依靠矿化垃圾床良好的生物脱氮作用,厌氧柱D1、D2、D3中NH3-N含量总体趋势为:NH3-ND1>NH3-ND3,NH3-ND1>NH3-ND2,准好氧d2、d3柱氨氮去除率均在90%以上,且厌氧-准好氧联合型生物反应器填埋场(AN-SABL)在实验产酸阶段低回灌频率(3 d/次)对氨氮的去除有利,而后期高回灌频率(1 d/次)更有利。     

垃圾龄对填埋场好氧修复供氧和加速稳定化效果的影响

填埋场好氧处理是一种有效的填埋场修复手段。采用模拟填埋反应器,搭配水气联合控制系统,探讨不同填埋龄垃圾好氧稳定化过程最佳氧气控制范围和污染物去除情况。结果表明新鲜垃圾和填埋龄分别为1,3,7年的垃圾最佳氧浓度调控范围分别为11%~14%、8%~14%、7%~15%和6%~17%。垃圾耗氧速率随填埋龄增加而降低。经过180~220 d的好氧处理,新鲜垃圾渗滤液BOD5和COD去除率均达到92%以上;而老龄垃圾渗滤液COD降解慢。处理后期各反应器ρ(BOD_5)/ρ(COD)<0.1,垃圾基本稳定。     

渗滤液回流对准好氧填埋产气过程影响研究

依据准好氧填埋的原理,构建了大型模拟填埋场。对准好氧填埋结构渗滤液回流情况下填埋气产气过程做了跟踪监测。定期测定填埋气中的组分浓度变化,结合填埋场渗滤液水质变化进行分析。结果表明准好氧填埋条件下进行渗滤液回流有利于减轻渗滤液的排放量且不会造成NH4+-N的累积。渗滤液回流可以加快甲烷的产气速度,渗滤液回流时的甲烷浓度约为不回流时的甲烷浓度的2倍。从而可加快垃圾的稳定化进程。     

填埋垃圾和渗滤液中CH4氧化菌的丰度研究

应用实时荧光定量聚合酶链式反应(Real-Time Quantitative Polymerase Chain Reaction,简称实时荧光定量PCR)技术对填埋场垃圾和渗滤液中CH₄氧化菌的pmoA基因进行定量分析. 结果表明:实时荧光定量PCR技术可用于渗滤液和垃圾中CH₄氧化菌的定量分析. 对于厌氧和准好氧填埋,初期渗滤液中CH₄氧化菌的数量均高于稳定期;准好氧填埋体渗滤液中CH₄氧化菌的数量均高于厌氧填埋体. 准好氧填埋垃圾中CH₄氧化菌的数量随着填埋龄的增加呈先增加后降低的趋势,并在填埋后的9个月左右达到最大值,与准好氧填埋体CH₄产生的规律相似. 同时,准好氧填埋垃圾中CH₄氧化菌的数量随着距导气管距离的增加而降低,但不同填埋时期的变幅不同,与准好氧填埋体O₂和CH₄的迁移规律有关. 此外,对渗滤液和垃圾样品的研究表明,准好氧填埋体垃圾填埋层内部存在大量的CH₄氧化菌,具有显著的CH₄氧化能力.      

生物反应器填埋场的发展及应用研究

缩短垃圾稳定化时间,并有效地收集和处理渗滤液及填埋气体,是促使传统卫生填埋法向生物反应器填埋场发展的主要因素。生物反应器填埋场通过回灌渗滤液等控制手段,改善填埋场内部微生化环境,加速填埋场稳定化进程。生物反应器填埋场的关键在于渗滤液收集系统、防渗系统、气体收集系统和渗滤液回灌系统。一些在运行的全规模生物反应器填埋场证明了这种操作方式能加快垃圾降解和填埋气体的产生,减少渗滤液处理量。然而还有一些经济和技术上的不确定性,包括持久有效性、压实度和氧化-还原环境等因素都需要进一步研究。     

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.