SMBBR-AF-SMBBR组合工艺处理高氨氮农药废水

采用特异性移动床生物膜反应器(SMBBR)和厌氧生物滤池(AF)组合工艺处理高氨氮农药废水。考察了HRT、pH和DO等工艺条件对SMBBR-AF-SMBBR组合工艺运行稳定期COD和氨氮去除率的影响。试验结果表明,在进水COD为2 408~7 440 mg/L、ρ(NH_4~+-N)为160.21~433.84 mg/L、TN为208.27~537.65 mg/L、HRT为8d、pH为8.0、DO为4 mg/L的条件下,处理后出水平均COD为342 mg/L,COD去除率达92.3%;ρ(NH_4~+-N)小于4.0mg/L,氨氮平均去除率为89.2%;TN小于50 mg/L,平均TN去除达83.0%。出水各指标均优于原A2O工艺出水。     

煤制乙二醇废水预处理装置的工业化调试

针对煤制乙二醇废水含高浓度硝酸盐氮的特点,设计了缺氧膨胀床(AEB)反应器预处理装置,并进行了工业化启动和调试运行,考察了其在反硝化连续流运行条件下的处理效果及工艺参数变化。结果表明,AEB反应器启动后,填料层生物膜挂膜快速且生长稳定。反应器在工业化调试阶段运行稳定,COD和TN的去除率和去除负荷较为稳定。在受到来水冲击后,AEB反应器处理效果稳定,出水可在短期内恢复正常。该技术的系统操控参数范围较广,易于工业化操控运行,在煤制乙二醇废水和其他含高浓度硝酸盐氮废水的处理中具有较大的推广价值。     

Biomonitoring in the Boulder River Watershed, Montana, USA: Metal Concentrations in Biofilm and Macroinvertebrates, and Relations with Macroinvertebrate Assemblage

Portions of the Boulder River watershed contain elevated concentrations of arsenic, cadmium, copper, lead, and zinc in water, sediment, and biota. We measured concentrations of As, Cd, Cu, Pb, and Zn in biofilm and macroinvertebrates, and assessed macroinvertebrate assemblage and aquatic habitat with the objective of monitoring planned remediation efforts. Concentrations of metals were generally higher in downstream sites compared with upstream or reference sites, and two sites contained metal concentrations in macroinvertebrates greater than values reported to reduce health and survival of resident trout. Macroinvertebrate assemblage was correlated with metal concentrations in biofilm and macroinvertebrates. However, macroinvertebrate metrics were significantly correlated with a greater number of biofilm metals (8) than metals in invertebrates (4). Lead concentrations in biofilm appeared to have the most significant impact on macroinvertebrate assemblage. Metal concentrations in macroinvertebrates were directly proportional to concentrations in biofilm, indicating biofilm as a potential surrogate for monitoring metal impacts in aquatic systems.     

Metals in vineyard soils of the Penedès area (NE Spain) after compost application

The application of organic wastes to improve soil physical characteristics in mechanized vineyards planted after land levelling is becoming a common practice in Mediterranean areas. It may be useful as an additional source of organic matter and nutrients, but these wastes could also have negative effects due to their metal content. The aim of the study was to evaluate the influence of compost application on soil metal contents in mechanized vineyard soils of the Spanish Mediterranean area, where this practice is repeated every three years. The study was carried out in a ten-year-old vineyard where the main soil type is Typic Calcixerept. Composted cattle manure was applied in alternate rows, at a rate of 40 Mgha(-1) dry-weight. Nine sampling points were located along the slopes of two plots: a levelled plot prepared for mechanization with large soil disturbance movements within the plot, and a plot of undisturbed soil. At each location, soil samples were taken in both treated and untreated soils. Total concentrations (digestion with aqua regia) and the extractable DTPA (Diethylene-triaminepentacetic)-CaCl2-TEA (Triethanolamine) fractions of Cu, Zn and Mn were analyzed in each sample. For Cu and Zn, the initial concentration was higher in the undisturbed plot. In both cases, total Cu and total Zn were positively affected by manure input and the concentration in treated soils was significantly higher than in untreated soil. For Mn, the initial concentration was higher in disturbed soils than in undisturbed ones, and although in both scenarios the concentrations increased with manure, no significant differences were found between treated and untreated soils. The extractable fraction also increased in treated versus untreated soils, although for Cu and Mn the extractable/total metal ratio was similar in treated and untreated soils. After one compost application, total metal contents increased significantly, particularly for Zn. Most of those metals are accumulated in the soil, due to the soil characteristics.     

不同浓度锌处理下水稻幼苗对镉的累积效应

为探究锌（Zn）对水稻镉（Cd）累积的影响及其根表铁膜所发挥的作用,选取Cd高累积型水稻品种中9优547（简称"Z547"）和Cd低累积型水稻品种金优402（简称"J402"）,采用温室水培试验,研究0、2、5、10、15和20 μmol/L等6个Zn浓度下水稻幼苗对Cd的累积效应,以及不同浓度Zn处理对根表铁膜生成量的影响.结果表明:①随着c（Zn）的增加,Z547和J402水稻幼苗生物量均呈先增后减的趋势,分别在c（Zn）为2和10 μmol/L时达到最大值.②Z547和J402水稻幼苗中w（Cd）均呈先降后增的趋势,分别在c（Zn）为5和2 μmol/L时达到最小值;当水稻幼苗中w（Cd）达到最小值时,Z547根和地上部中w（Cd）分别为31.65和11.47 mg/kg,J402根和地上部中w（Cd）分别为22.58和14.36 mg/kg.③不同浓度Zn处理下水稻幼苗各部位中w（Cd）均与根表铁膜中w（Mn）、w（Fe）、w（Fe+Mn）呈显著正相关,高铁膜处理水稻幼苗中w（Cd）显著高于低铁膜处理,表明根表铁膜生成量的增加会促进Cd在水稻幼苗中的累积.研究显示,当c（Zn）较低时,c（Zn）的增加会抑制水稻幼苗对Cd的累积;当c（Zn）较高时,c（Zn）的增加会促进水稻幼苗对Cd的累积,而Zn可通过控制根表铁膜的生成来影响水稻幼苗对Cd的累积.      

土壤调理剂对土壤-水稻系统Cd、Zn迁移累积的影响及健康风险评价

选取湖南省长沙市北山镇某中重度Cd污染稻田,研究了土壤调理剂(石灰石+偏高岭土+钙镁磷肥)对稻田土壤重金属Cd、Zn的钝化效果,以及对水稻各部位累积Cd和Zn的影响,并进行了Cd的健康风险评价.结果表明,使用土壤调理剂提高了稻田土壤p H值.Cd的CaCl_2提取态含量降低了0.9%~24.1%,Zn的CaCl_2提取态含量降低了22.5%~69.6%.土壤调理剂显著降低了水稻糙米中Cd与Zn的含量,与对照相比分别降低了10.8%~47.3%、10.3%~17.5%;土壤调理剂对水稻糙米Cd的吸收和累积的影响要远大于Zn,水稻糙米中的Cd/Zn比随着土壤调理剂施用量的增加而显著降低.研究区大米重金属Cd目标危害系数THQ值大于1,说明当地人群通过食用大米途径摄入重金属Cd存在健康风险.土壤调理剂有效地抑制了水稻植株对土壤中Cd的吸收,并降低了Cd/Zn比,使糙米中的Cd含量显著降低,从而降低了当地人群通过食用大米途径摄入重金属Cd的健康风险.     

Distribution of Iron, Manganese, Zinc and Atrazine in Groundwater in Parts of Palar and Cheyyar River Basins, South India

A study was carried out in a part of Palar and Cheyyar river basin to evaluate the current status of iron, manganese, zinc and atrazine concentrations, their origin and distribution in groundwater. Groundwater samples were collected during post-monsoon (March 1998 and February 1999) and pre-monsoon (June 1999) periods from 41 sampling wells distributed throughout the study area. The groundwater samples were analyzed for trace metals using AAS and atrazine using HPLC. The concentration of the trace elements in groundwater is predominant during pre-monsoon period. Distribution pattern indicates that the concentration of these elements increases from west to northeast and towards Palar river. Lower concentrations in the central part may be due to recharge of fresh water from the lakes located here. During most of the months, as there is no flow in Palar river, the concentrations of trace elements in groundwater are high. Drinking water standards indicate that Mn and Zn cross the permissible limit recommended by EPA during the pre-monsoon period. A comparison of groundwater data with trace element chemistry of rock samples shows the abundance of trace elements both in the rock and water in the order of Fe > Mn > Zn and Fe > Zn > Mn. This indicates that iron in groundwater is derived from lithogenic origin. Further, Fe, Mn and Zn have good correlation in rock samples, while it is reverse in the case of water samples, indicating the non-lithogenic origin of Mn and Zn. Atrazine (a herbicide) was not detected in any of the groundwater samples in the study area, perhaps due to low-application rate and adsorption in the soil materials.     

Cu、Pb、Zn火焰原子吸收多谱线分析在环境监测中的应用

对铜的 3条谱线 (2 49.2 nm、2 61 .4nm,3 2 4.8nm ) ,铅的 2条谱线 (2 83 .3 nm、2 1 7.0 1 nm )以及锌的 2条谱线(3 0 7.6nm、2 1 3 .9nm ) ,共 7条谱线的灵敏度、检测限、线性范围进行了归纳性总结 ,并对多种共存元素可能存在的干扰情况进行了研究 ,认为利用元素不同分析谱线的分析灵敏度差异 ,根据被测元素在样品消解液中含量 ,选择合适的谱线进行分析 ,既降低工作强度 ,又能获得满意结果     

微波消解-原子吸收光度法测定土壤中铜锌铅镉镍铬

用微波消解－原子吸收光度法测定土壤中铜，锌，铅，镉，镍和铬。通过硝酸－氢氟酸－过氧化氢体系消解液对土壤样品消解，选择出微波最佳消解条件。对硝酸－盐酸－过氧化氢体系消解液和硝酸－氢氟酸－过氧化氢体系消解液进行消解对比试验，发现前者不能将土壤样品完全消解，后者能将样品消解完全，但需将消解液中剩余的酸赶尽，否则测定结果将明显偏低。微波消解土壤与传统电热消解相比，操作简便快速，可提高工作效率。     

Effect of temperature on single and competitive adsorptions of Cu(II) and Zn(II) onto natural clays

This study conducted a combined adsorption-sequential extractionanalysis (CASA), by which five phases (i.e., exchangeable, carbonate, Mn-Oxide, organic, and Fe-Oxide phases) of adsorbed heavy metals were analyzed, to investigate temperature effects on single and competitive adsorptions of Zn(II) and Cu(II) ontonatural clays. In the case of single adsorption of Zn, the exchangeable phase adsorption decreased from 65 to 40%, but thecarbonate phase adsorption increased from 30 to 40%, with an increase in temperature from 15 to 55 °C. However, in itscompetitive adsorption with Cu, Zn was mostly present in the exchangeable phase (over 90%), and with an increase in temperature, the exchangeable phase adsorption decreased only 10%. In the case of Cu, over 50% among the total amount of adsorption was present in the carbonate phase in both cases ofsingle and competitive adsorptions. The carbonate phaseadsorption of Cu increased from 56 to 61% and from 60 to 66% in single and competitive adsorptions, respectively, with atemperature increase. These results show that in the case of Zn,the major mechanism of retention in natural clay soils might beexchangeable phase adsorption, especially in the case of competitive adsorption with Cu. However, in the case of Cu, the major mechanism might be carbonate phase adsorption, which is known to be a more immobile phase than exchangeable phase adsorption. It seems that the adsorption of Zn and Cu onto natural clays is an endothermic reaction, which represents thatthe adsorption equilibrium constants and capacities increase with a temperature increase, with the exception of exchangeablephase adsorption.