螺蚌和沉水植物搭配对微污染水体的净化作用

通过开展单植不同种类沉水植物及"不同种类的沉水植物+螺蚌"组合搭配对微污染水体的净化能力对比研究,寻求系统稳定性最好、水质净化最佳的组合。2013年8月至2014年3月间的水箱小试研究结果表明,"铜锈环棱螺+椭圆背角无齿蚌+轮叶黑藻+篦齿眼子菜"组合的水质净化作用最佳,对CO D、TN、TP去除率分别为58.79%、64.30%和88.57%,对浮游生物的抑制效果最明显,水箱里基本无水绵及浮萍生长,轮叶黑藻长势较篦齿眼子菜好、生长逐渐占优势。2014年5月—8月的中试研究进一步验证水箱小试的结论,COD、TN和TP的平均去除率分别为57.93%、60.12%和49.28%,轮叶黑藻长势更好。     

巢湖最大入湖河流背角无齿蚌中多环芳烃的含量、来源及风险评价

测定了巢湖最大入湖河流杭埠河及其支流丰乐河中背角无齿蚌(Anodonta woodiana)体内16种美国环境保护署(USEPA)优先控制的多环芳烃(PAHs)含量,分析了其来源,并对其生态风险和致癌风险进行评估。结果表明,16种PAHs在背角无齿蚌中均有检出,总质量浓度为707.8~1 614.6ng/g(以干重计)。从PAHs组成来看,低环(2~3环)、中环(4环)和高环(5~6环)的PAHs分别占29.8%、19.5%、50.7%,其中茚并[1,2,3-cd]芘浓度最高。来源分析表明,杭埠河及其支流丰乐河中背角无齿蚌体内的PAHs主要来源于草、木、煤等燃料的燃烧。PAHs的生态风险和致癌风险评价结果显示,杭埠河及其支流丰乐河中背角无齿蚌体内的PAHs具有一定的风险,应当引起重视。     

背角无齿蚌对养鱼水体的净化效果

通过建立微型生态系统,研究了不同养殖密度和处理时间条件下,背角无齿蚌(Anodonta woodiana)对大宗淡水鱼养殖水体理化指标和营养盐的影响及净化特征。研究结果表明,背角无齿蚌对水体p H、CODMn和NH+4-N的影响不明显;电导率、总固溶物、NO-2-N、DTP、PO3-4-P和DOC呈升高的趋势;DO随蚌养殖密度和时间的增加而降低;能够显著降低水体的浊度、Chl-a、TN、NO-3-N和TP含量(P0.05),最大去除率分别为90.9%、90.8%、24.1%、23.1%和23.4%。响应面优化分析显示,蚌养殖密度和处理时间分别为21 ind./m3和15.35 d、25 ind./m3和10 d时,对NO-3-N、TP的去除率可进一步提升至42.6%和35.0%。本研究表明,背角无齿蚌可以用于养鱼水体的水质净化。     

3种沉水植物对再生水水质维护效果的比较

为了防止再生水利用时出现富营养化现象,选用苦草(Vallisneria natans(Lour.)Hara)、金鱼藻(Ceratophyllum demersum L.)和穗状狐尾藻(Myriophyllum spicatum L.)3种沉水植物,配合投加鲢鱼(Hypophthalmichthys molitrix)和椭圆背角无齿蚌(Anadonta woodiana elliptica),对再生水水质进行维护,对比不同组合对再生水的净化和保持效果。结果表明:金鱼藻能较好维护再生水的水质稳定,实验中后期COD、氨氮分别在30、0.4mg/L以下,而且金鱼藻可较好地抑制浮游植物的生长,叶绿素a基本都小于叶绿素a水华阈值(40μg/L),同时鲢鱼和椭圆背角无齿蚌的投加能完善生态系统,并维护再生水pH的稳定。     

背角无齿蚌净化养殖水体中的重金属

通过建立微型生态系统,研究不同养殖密度和处理时间的背角无齿蚌(Anodonta woodiana)对大宗淡水鱼养殖池塘水体中重金属的净化效果。结果显示,背角无齿蚌对重金属的净化效果受到处理时间和养殖密度的显著影响(P0.05)。其对Mn、Cu、As和Cd的影响总体不明显,Ba的含量增加(P0.05),然而能够显著降低Al、Cr、Fe、Ni、Zn和Mo的含量(P0.05),最大去除率分别为63.0%、78.0%、12.7%、100%、80.6%和4.8%,而且响应优化分析显示,蚌养殖密度和处理时间的配比分别为31 ind./m~3和22.77 d、40 ind./m~3和19.78 d时,对Cr和Zn的去除率可提升至80.3%和81.8%。本研究表明背角无齿蚌有潜力用于养鱼水体重金属的净化。     

鲢鳙放养水平对淀山湖浮游植物群落影响的围隔实验

在淀山湖进行放养不同密度鲢、鳙的围隔实验（密度水平梯度设置为0、40、80和120 g/m3）,探索鲢、鳙的现场控藻效果。结果表明,实验后期（8—9月）,鲢、鳙放养密度为80 g/m3和120 g/m3的围隔对叶绿素a的去除效果显著（P〈0.05）;且放养密度为80 g/m3的围隔蓝藻比例降幅最明显。鲢、鳙对较大个体藻...     

贵州省已建城镇污水处理厂建设及运行状况

"十一五"期间,贵州省开展了大规模的城镇污水处理厂建设,主要采用了以氧化沟、A/O工艺和SBR及改良工艺等具有脱氮除磷功能、技术成熟的工艺,建设规模多在0.5万m3/d以下,单位平均建设投资4 069.75元/m3,单位综合能耗平均0.35 k Wh/m3,单位平均药耗0.41 g/m3,单位运行成本多在0.60元/m3以上,污水平均处理率82.01%,平均处理负荷率73.19%,处理出水基本达到城镇污水处理厂污染物排放标准(GB18918-2002)一级B标准的要求,取得了较好的减排效果,但部分污水处理厂存在工艺技术的匹配性等问题,建议"十二五"期间加强已建污水处理厂工艺技术和设施的改造升级。     

三峡库区城市污水处理厂工艺特征分析

为了分析三峡库区(重庆)城市污水处理厂的工艺特性,对库区现有45座城市污水处理厂进行了调研。发现库区以5万m3/d以下规模的污水处理厂为主,占总数的89%。A/A/O系列工艺、氧化沟系列工艺和SBR及其变型工艺为主流主体工艺,其中占总数64%的污水处理厂选用了氧化沟系列工艺。水质参数的设置与工艺密切相关。污水中无机物含量较高,59%的污水处理厂的MLSS在4~6 g/L之间,71%的污水处理厂的MLVSS/MLSS在0.7以下。三峡库区城市污水处理厂进水水质波动大,碳源较充足,可生化性较好。另外,总结了污水处理厂运行中易出现的问题及建议措施。     

鲢鱼放养控制北京城市河湖水华试验研究

介绍了利用鲢鱼控制北京城市河湖水华的试验研究,通过不同放养密度(0、17、51和103 g/m3)的现场围隔试验,对鲢鱼放养对水体水质和浮游生物的影响进行了分析.研究结果表明,鲢鱼放养使有鱼围隔中浮游生物量极低,从而使浮游植物基本不受浮游动物影响,而直接受鱼类影响;同时,中等密度(51 g/m3)的鲢鱼放养使水华蓝藻和微小藻的生长均得到了有效抑制,使藻类生物量最低.     

广西城镇污水处理厂建设和运行的现状分析

全区108座污水处理厂建设规模、工艺、投资和运行成本统计表明,广西城镇污水处理厂以小型污水处理厂为主,处理工艺多采用氧化沟、A2/O、SBR及其变种工艺;5～10万m3/d规模污水处理单位建设投资以氧化沟、A2/O、SBR及其变种工艺较省,2～5万m3/d规模以氧化沟、MSBR工艺较省,2 m3/d以下规模以硅藻土、人工湿地和人工快渗工艺较为经济;2～10万m3/d规模污水处理厂各工艺运行成本多介于0.3～0.4元/m3,2万m3/d以下规模人工快渗和人工湿地工艺的运行费用介于0.2～0.3元/m3。不同规模、不同工艺、不同排放标准污水处理厂的投资建设、运行成本和出水水质各异,因此,污水处理厂应因地制宜选择适宜工艺技术、规模及排放标准,有效提高设施运行负荷率和污染物的去除率。     

Field and laboratory studies of the fate and enantiomeric enrichment of venlafaxine and O-desmethylvenlafaxine under aerobic and anaerobic conditions

The stereoselectivity of R,S-venlafaxine and its metabolites R,S-O-desmethylvenlafaxine, N-desmethylvenlafaxine, O,N-didesmethylvenlafaxine, N,N-didesmethylvenlafaxine and tridesmethylvenlafaxine was studied in three processes: (i) anaerobic and aerobic laboratory scale tests; (ii) six wastewater treatment plants (WWTPs) operating under different conditions; and (iii) a variety of wastewater treatments including conventional activated sludge, natural attenuation along a receiving river stream and storage in operational and seasonal reservoirs. In the laboratory and field studies, the degradation of the venlafaxine yielded O-desmethylvenalfaxine as the dominant metabolite under aerobic and anaerobic conditions. Venlafaxine was almost exclusively converted to O-desmethylvenlafaxine under anaerobic conditions, but only a fraction of the drug was transformed to O-desmethylvenlafaxine under aerobic conditions. Degradation of venlafaxine involved only small stereoisomeric selectivity. In contrast, the degradation of O-desmethylvenlafaxine yielded remarkable S to R enrichment under aerobic conditions but none under anaerobic conditions. Determination of venlafaxine and its metabolites in the WWTPs agreed well with the stereoselectivity observed in the laboratory studies. Our results suggest that the levels of the drug and its metabolites and the stereoisomeric enrichment of the metabolite and its parent drug can be used for source tracking and for discrimination between domestic and nondomestic wastewater pollution. This was indeed demonstrated in the investigations carried out at the Jerusalem WWTP.     

骆马湖富营养化和生态状况调查与评价

为了了解骆马湖水质状况，在2005年对骆马湖富营养化状态和生态特性进行了调查，并结合“十五”期间的监测资料进行了分析。2005年骆马湖水体中总氮和总磷的平均值超《地表水环境质量标准》（GB3838-2002）中Ⅲ类，超标情况分别为0．78倍和0．54倍，达到湖库特定项目Ⅳ类水标准，骆马湖处于轻度富营养化状态。对骆马湖生态特征分析表明，由于该湖泊的形态以及“藻型浊水状态”和“泥沙型浊水状态”交替出现，遏制了湖水从高营养盐含量向全面富营养化状态演变，保障了底栖动物的良好生长环境，从而形成了骆马湖独特的环境生态平衡。     

Copper-catalyzed chlorination and condensation of acetylene and dichloroacetylene

The chlorination and condensation of acetylene at low temperatures is demonstrated using copper chlorides as chlorinated agents coated to model borosilicate surfaces. Experiments with and without both a chlorine source and borosilicate surfaces indicate the absence of gas-phase and gas-surface reactions. Chlorination and condensation occur only in the presence of the copper catalyst. C₂ through C₈ organic products were observed in the effluent; PCDD/F were only observed from extraction of the borosilicate surfaces. A global reaction model is proposed that is consistent with the observed product distributions. Similar experiments with dichloroacetylene indicate greater reactivity in the absence of the copper catalyst. Reaction is observed in the gas-phase and in the presence of borosilicate surfaces at low temperatures. The formation of hexachlorobenzene is only observed in the presence of a copper catalyst. PCDD/F were only observed from extraction of the borosilicate surfaces. A global reaction model is proposed for the formation of hexachlorobenzene from dichloroacetylene.     

Sources and distribution of polychlorinated-dibenzo-p-dioxins and -dibenzofurans in soil and sediment from the Yellow Sea region of China and Korea

Polychlorinated-dibenzo-p-dioxins and -dibenzofurans (PCDD/Fs) were measured in soils and sediments from the Yellow Sea region. Korean soils and sediments mostly contained detectable PCDD/Fs and showed a widespread distribution among locations. Soil and sedimentary PCDD/Fs from China were comparable to or less than those in Korea. The patterns of relative concentrations of individual congeners in soils were different between the two countries, but similar in sediments. Sources of PCDD/Fs in China and Korea were found to be independent of each other and their distributions reflected matrix-dependent accumulation. Spatial distribution indicated some point sources in Korea while Chinese sources were more widespread and diffuse. PCDD/Fs measured in the coastal areas of the Yellow Sea were comparable to or less than those previously reported in for eastern Asia. However, ∑TEQs in soils and sediments were near to or, in some cases exceeded environmental quality guidelines.     

Aerobic and anaerobic degradation of profluralin and trifluralin

Abstract

The degradation of profluralin [N‐(cyclopropylmethyl)‐α,α,α‐trifluoro‐2,6‐dinitro‐N‐propyl‐]p‐toluidine] and trifluralin (α,α,α‐trifluoro‐2,6‐dinitro‐N,N‐dipropyl‐p‐toluidine) was studied under aerobic and anaerobic soil conditions. Three soils (Goldsboro loamy sand, Cecil loamy sand, Drummer clay loam) were each treated with 1 ppmw herbicide; anaerobic conditions were maintained by flooding. Soil samples were extracted monthly and subjected to TLC analysis. No degradation was detected in sterile controls. Aerobic degradation of both herbicides was greatest in the Cecil loamy sand soil over the entire incubation period. Degradation of profluralin in Cecil soil under aerobic conditions was 86 percent after 4 months with three products detected; 83 percent of the trifluralin was degraded with two products detected. Anaerobic degradation accounted for 72 percent of the profluralin and 78 percent of the trifluralin after 4 months. Degradation of both herbicides increased with incubation time for the first 3 months and decreased slightly thereafter. Generally there was more extensive degradation (percent and in number of products formed) of profluralin than trifluralin under the conditions tested. More degradation products were detected for both herbicides under aerobic conditions than under anaerobic conditions.     

Quantification of carbamazepine and atrazine and screening of suspect organic contaminants in surface and drinking waters

A new approach for the identification of suspect trace organic contaminants in drinking and surface waters is presented. Samples were initially analyzed using a target determination method for two contamination tracers, carbamazepine (CBZ) and atrazine (ATZ). This method used offline solid-phase extraction and online solid-phase extraction techniques coupled to liquid chromatography-triple quadrupole mass spectrometry to accelerate the sample preparation process and improve method performance. CBZ and ATZ were found respectively in 31% and 56% of the samples, and concentrations were usually <20 ng L⁻¹. These samples were re-analyzed with a similar method on a quadrupole time-of-flight mass spectrometer to identify suspect contaminants by means of exact mass measurements and isotope patterns. A database of 264 common organic contaminants was built and used in conjunction with a Molecular Feature algorithm to identify the presence of these substances in drinking and surface water collected from different sources at various locations across Canada. Several organic contaminants were identified in the samples, but only the presence of caffeine, desethylatrazine, simazine and venlafaxine could be verified by comparison to pure standards. The presence of desethylatrazine was also confirmed by MS/MS experiments. These results suggest that target analysis for tracers of organic contamination may be a helpful tool to prioritize samples which should be further screened for suspect contaminants. This study also shows that the combination of separation techniques (offline and online SPE, LC) contribute to advance the applicability of high-resolution mass spectrometry for the identification of trace organic contaminants by accelerating the preparation step, reducing complexity and increasing analyte concentrations for optimal detection.     

Persistence and dissipation kinetics of trifloxystrobin and tebuconazole in onion and soil

The persistence and dissipation kinetics of trifloxystrobin and tebuconazole on onion were studied after application of their combination formulation at a standard and double dose of 75 + 150 and 150 + 300 g a.i. ha^?1. The fungicides were extracted with acetone, cleaned-up using activated charcoal (trifloxystrobin) and neutral alumina (tebuconazole). Analysis was carried out by gas chromatograph (GC) and confirmed by gas chromatograph mass spectrometry (GC-MS). The recovery was above 80% and limit of quantification (LOQ) 0.05 mg kg^?1 for both fungicides. Initial residue deposits of trifloxystrobin were 0.68 and 1.01 mg kg^?1 and tebuconazole 0.673 and 1.95 mg kg^?1 from standard and double dose treatments, respectively. Dissipation of the fungicides followed first-order kinetics and the half life of degradation was 6–6.6 days. Matured onion bulb (and field soil) harvested after 30 days was free from fungicide residues. These findings suggest recommended safe pre-harvest interval (PHI) of 14 and 25 days for spring onion consumption after treatment of Nativo 75 WG at the standard and double doses, respectively. Matured onion bulbs at harvest were free from fungicide residues.     

剩余污泥浓缩脱水投药量优化和模型建立

应用高分子阳离子絮凝剂（CPF-100）和聚丙烯酰胺（PAM）对污水厂剩余污泥进行浓缩脱水实验，研究表明：CPF-100的浓缩脱水效果优于PAM；当CPF-00投加量为1．16‰时，污泥沉降性能改善程度为37．51％；且在CPF-100投加量逐渐增大的初始阶段，污泥沉降性能改善程度随投加量的增加而增大，但CPF-100投加量也不宜过大，当CPF-100投加量超过1．16‰后，反而会使浓缩脱水效果变差。同时，建立了污泥沉降性能改善程度与絮凝剂CPF-100投加量、沉降时间之间的数学模型，其能较好地反映污水厂剩余污泥的浓缩脱水效果。     

Effects of compositional heterogeneity and nanoporosity of raw and treated biomass-generated soot on adsorption and absorption of organic contaminants

A biomass-generated soot was sequentially treated by HCl-HF solution, organic solvent, and oxidative acid to remove ash, extractable native organic matter (EOM), and amorphous carbon. The compositional heterogeneity and nano-structure of the untreated and treated soot samples were characterized by elemental analysis, thermal gravimetric analysis, BET-N₂ surface area, and electron microscopic analysis. Sorption properties of polar and nonpolar organic pollutants onto the soot samples were compared, and individual contributions of adsorption and absorption were quantified. The sorption isotherms for raw sample were practically linear, while were nonlinear for the pretreated-soot. The removal of EOM enhanced adsorption and reduced absorption, indicating that EOM served as a partitioning phase and simultaneously masked the adsorptive sites. By drastic-oxidation, the outer amorphous carbon and the inner disordered core of the soot particles were completely removed, and a fullerene-like nanoporous structure (aromatic shell) was created, which promoted additional π-π interaction between phenanthrene and the soot.     

Sorption and Desorption Behavior of Chloroanilines and Chlorophenols on Montmorillonite and Kaolinite

The bioavailability of pollutants, pesticides and/or their degradation products in soil depends on the strength of their sorption by the different soil components, particularly by the clay minerals. This study reports the sorption-desorption behavior of the environmentally hazardous industrial pollutants and certain pesticides degradation products, 3-chloroaniline, 3,4-dichloroaniline, 2,4,6-trichloroaniline, 4-chlorophenol, 2,4-dichlorophenol and 2,4,6-trichlorophenol on the reference clays kaolinite KGa-1 and Na-montmorillonite SWy-l. In batch studies, 2.0 g of clay were equilibrated with 100.0 mL solutions of each chemical at concentrations ranging from 10.0 to 200.0 mg/L. The uptake of the compounds was deduced from the results of HPLC-UV-Vis analysis. The lipophilic species were best retained by both clay materials. The most lipophilic chemical used in the study, 2,4,6-trichloroaniline, was also the most strongly retained, with sorption of up to 8 mg/g. In desorption experiments, which also relied on HPLC-UV-Vis technique, 2,4,6-trichloroaniline was the least desorbed from montmorillonite. However, on kaolinite all of the compounds under study were irreversibly retained. The experimental data have been modelled according to the Langmuir and Freundlich isotherms. A hypothesis is proposed concerning the sorption mechanism and potential applications of the findings in remediation strategies have been suggested.