Cu~(2+)/吡啶/H_2O_2对直接大红4BE的快速脱色研究

为了明确影响Cu2+/吡啶/H2O2对模拟染料(DR4BE)废水脱色的主要因素,采用动力学分析、正交和Box-Behnken实验设计研究了不同溶液pH、Cu2+、吡啶、H2O2浓度及Cu2+、吡啶和H2O2组合对初始脱色速率常数和最终脱色率的影响.同时,采用自由基抑制、H2O2催化分解实验探索了Cu2+/吡啶/H2O2对染料的脱色机理.结果发现,Cu2+/吡啶/H2O2能有效使DR4BE快速脱色,脱色效率远高于Cu2+/H2O2;pH是影响初始脱色速率最重要的因素,吡啶、Cu2+及pH是影响最终脱色率最重要的因素;溶液pH在7.0左右时有利于该脱色过程的快速进行.Cu2+与吡啶的交互作用相对较强,吡啶、Cu2+与H2O2的交互作用相对较弱.羟基自由基氧化是Cu2+/吡啶/H2O2对染料DR4BE初始快速脱色的主要机理.研究结果还表明,Cu2+/吡啶/H2O2体系可用于中性条件下染料废水的快速脱色处理.     

Particle properties in granular activated carbon filter during drinking water treatment

The elemental composition and bacteria attached in particles were investigated during granular activated carbon (GAC) filtration.The experimental results showed that trapped influent particles could form new,larger particles on GAC surface.The sloughing of individuals off GAC surface caused an increase in effluent particles in the size range from 5 to 25 μm.The selectivity for element removal in GAC filters caused an increasing proportion of metallic elements in the effluent particles.The distribution of molar ratio indicated a complicated composition for large particles,involving organic and inorganic substances.The organic proportion accounted for 40% of total carbon attached to the particles.Compared with dissolved carbon,there was potential for the formation of trihalomethanes by organic carbon attached to particles,especially for those with size larger than 10 μm.The pure carbon energy spectrum was found only in the GAC effluent and the size distribution of carbon fines was mainly above 10 μm.The larger carbon fines provided more space for bacterial colonization and stronger protection for attached bacteria against disinfection.The residual attached bacteria after chorine disinfection was increased to 10 2-10 3 CFU/mL within 24 hours at 25°C.     

Shrinkage and fragmentation of grasslands in the West Songnen Plain,China

In the past century, especially the past five decades, the grasslands of the West Songnen Plain, Northeast China, were rapidly converted into croplands and salinized wasteland, and experienced a fragmentation process that is still ongoing. Almost no information is available on the spatial-temporal changes of grasslands in this area. In this study, grassland cover change, agricultural reclamation and salinized wasteland expansion were investigated during the past five decades. Grassland fragmentation was studied based on four landscape metrics. The grassland cover change was detected from a time series of topographic maps from 1954, satellite images of Landsat TM in 1986, 1995, and 2000 using remote sensing and geographic information systems (GIS). In addition, the land use changes were analyzed using a transition matrix of land use types, while the driving forces were explored according to climatic changes and socioeconomic developments. The results indicated a significant decrease in grassland area. Of the 1 418 945 ha of native grassland in 1954, approximately 64% was removed by 2000, while the number of patches (NP) increased from 865 to 2035 and the mean patch size (MPS) decreased from 1640 ha to 252 ha. During the whole study period, the average annual decrease rate of grassland was 34 894 ha/year. Cropland and salinized wasteland were the two main land use types into which grassland converted. During the past decades, obvious climatic changes occurred, which supplied a favorable potential environment for agricultural development but damaged grassland productivity. On the other hand, population, GDP and livestock number increased significantly as grassland quality decreased. According to the results, the shrinkage and fragmentation of grasslands may well be explained by socioeconomic development and aided by changing climatic conditions.     

厌氧氨氧化工艺处理高氨氮养殖废水研究

以典型高浓度养殖废水经UASB-短程亚硝化工艺处理后的出水为对象,采用厌氧氨氧化工艺进行脱氮处理研究.以反硝化污泥启动厌氧氨氧化反应器,在此基础上,通过试验确定最佳进水氨氮负荷应处于0.2 kg/(m³·d)左右,系统的HRT定为2 d;通过对系统运行条件研究发现,最佳运行条件为：pH为7.50左右,温度为30℃且系统不需投加有机碳源.在优化条件下,系统最终氨氮去除率能达到85％以上,亚硝态氮去除率达到95％以上,系统运行效果良好,且具有重现性.最后通过动力学理论分析得出氨氮的降解速率为0.012 6 d^－1,亚硝态氮的降解速率为0.013 1 d^-1.通过研究以期为后续工艺、神经网络模拟及“UASB-短程亚硝化-厌氧氨氧化-土地系统"组合新工艺的工程推广应用提供一定的理论依据.     

生活污水中环境雌激素的厌氧消化行为特征及环境风险评价

为了研究生活污水中典型环境雌激素（estrogenic endocrine disruptors, EEDs）在上流式厌氧污泥床（upflow anaerobic sludge blanket, UASB）和厌氧滤池（anaerobic filter, AF）中的行为特征和去除机制,采用固相萃取（SPE）LC/MS/MS分析方法,测定了9种EEDs的浓度和污泥吸附量,利用壬基酚当量（nonylphenol equivalent quantity, NEQ）进行了环境风险评价.结果表明,厌氧污泥对各EEDs的吸附能力与该物质的lgK_ow煤头肿映ざ认喙兀籙ASB对雌二醇（E2）和大豆苷元的去除率分别达83.2%和90.4%,AF对染料木素的去除率达81.6%; 9种EEDs在UASB和AF中的污泥水分配系数（K_p）分别为0.15～23.3和0.05～159.67;综合分析去除率和K_p值数据,揭示了生物降解是大豆苷元、染料木素、双酚A（BPA）和雌三醇（E3）的主要去除途径;出水的NEQ均小于美国EPA的壬基酚水质标准（28　μg·L^－１,小时平均浓度标准）,表明EEDs经厌氧处理后其环境风险有所降低.     

PFOS/PFOA对斑马鱼(Danio rerio)胚胎致毒效应研究

采用斑马鱼胚胎毒性测试方法,研究了PFOA/PFOS对斑马鱼的急性毒性和生命早期阶段生长发育的影响.结果表明,PFOS/PFOA对斑马鱼有明显毒性作用,LC₅₀(48 h)分别为1005 mg/L和107 mg/L,LC₅₀(96　h)分别为499 mg/L和71 mg/L.PFOS/PFOA抑制斑马鱼胚胎发育,可导致胚胎发育畸形,甚至死亡,高浓度(＞240 mg/L)PFOS损伤细胞膜,导致胚胎分裂中的细胞发生自溶而卵凝结死亡,抑制胚胎原肠胚的形成.在各种亚致死效应中,脊柱畸形对PFOS暴露最敏感,其EC₅₀=9.14 mg/L,PFOA暴露最敏感亚致死性毒理学终点为96　h孵化,对应EC₅₀=328.0 mg/L.PFOA/PFOS导致胚胎发育延迟,具有发育毒性.     

碳源类型对A~2O系统脱氮除磷的影响

采用52.5 L的A2O反应器,以乙酸和丙酸分别作为进水唯一碳源,系统研究了进水碳源类型对脱氮除磷和代谢过程的影响.结果表明,在进水COD为250 mg/L左右,NH+4-N为52 mg/L左右的条件下,原水碳源类型对TN的去除影响不大,系统TN去除率均在65%左右.进水碳源类型对TP的去除及相应污泥中PHA的类型、含量和代谢及糖原的变化影响较大.乙酸为唯一碳源时,厌氧区放磷浓度较高,污泥中PHA的成分主要为PHB和PHV,两者在厌氧区的合成量差别不大,PHB在随后的反应过程中变化较大,对除磷代谢过程起主要作用,而PHV的变化较小.丙酸作为进水唯一碳源时,厌氧区的放磷浓度偏低,主要合成PHV,几乎不含PHB,PHV在随后吸磷过程中浓度变化较大,对除磷代谢起主要作用,而且出水TP浓度偏低.碳源类型对污泥中糖原的代谢也有影响,乙酸为碳源时糖原的含量高,变化范围也较大,丙酸为碳源时糖原的变化幅度较小.在同步脱氮除磷系统中,与乙酸相比,丙酸是一种更合适的碳源.     

基质种类对活性污泥絮体性状的影响

利用葡萄糖、淀粉、乙酸钠和苯酚4种典型基质,分别在4个相同的序批式反应器(Sequencing Batch Reactor,SBR)中培养活性污泥,并研究了基质种类对活性污泥絮体性状的影响.结果表明,以葡萄糖为底物培养的活性污泥胞外多糖含量最少,而苯酚所培养的活性污泥胞外蛋白质最多;从形成的EPS总量来看,苯酚最多,乙酸钠次之,葡萄糖和淀粉较少.不同基质培养的污泥Zeta电位也有一定差别,这是由EPS中多糖和蛋白质的比例不同造成的.红外分析表明,4种基质培养的污泥EPS中的主要基团较为相似,羧基、醇羟基、羧酸、酰胺和多聚糖均是EPS中的主要基团.此外,进水基质对活性污泥絮体的粒度分布及分形结构也有重要影响.     

高锰酸钾预氧化混凝去除水中颤藻的试验研究

采用KMnO4对颤藻氧化,再接种到培养液中进行培养,根据达到对数生长期的时间,考察KMnO4预氧化对颤藻生长活性的影响,并通过显微镜观察藻细胞的破裂情况,同时采用聚合氯化铝(PAC)对KMnO4预氧化水体进行混凝处理,结果表明:KMnO4对颤藻有很好的氧化效果,不同浓度KMnO4对颤藻生长活性的抑制时间不同;在投加量为2 mg/L以下时,预氧化没有破坏颤藻的细胞结构;模拟含藻水在KMnO4预氧化后采用PAC混凝优于单加PAC的除藻效果.     

二氧化锰氧化降解金霉素的动力学研究

研究了金霉素(CTC)在二氧化锰(MnO2)作用下的氧化降解过程,并讨论了初始MnO2浓度、体系pH及温度对降解反应的影响.无MnO2存在时,CTC没有发生降解.但是当体系中存在MnO2时,CTC浓度开始迅速下降,反应后期降解速率逐渐变慢;同时体系中二价锰离子(Mn2+)浓度逐渐升高,表明MnO2可以降解CTC,该过程是一个氧化还原反应.采用草酸溶解MnO2和过滤2种不同的方法终止反应,对比2种方法所得的结果,可以发现该反应过程中,开始阶段降解作用占主导地位,在反应达到平衡后吸附作用才明显.CTC的降解速率随着MnO2初始浓度的增加和体系温度的升高均显著加快.反应体系的pH能强烈影响CTC的氧化降解,降解速率随着pH的升高而明显降低.这是由于CTC随体系pH由3.77升高到7.41时,分别以阳离子、中性形态和阴离子的形式存在;而-δMnO2(pHzpc=2.25)表面在pH3.77的整个范围内均呈现为负电性.因此随pH升高,阴离子形态的CTC逐渐增多,导致其在MnO2表面的吸附作用减弱,从而使降解速率变缓.