生活垃圾填埋场封场后种植植物中重金属迁移研究

在上海老港生活垃圾填埋场填埋单元封场的覆盖土中掺混了矿化垃圾种植植物,分析Cd、Pb、Cu、Zn 4种重金属在土壤和植物中的迁移变化,研究表明:(1)覆盖土土质从一般耕作土变成肥沃土壤;覆盖土和种植混合土重金属Cd、Pb、Cu、Zn中Cd、Pb含量相近,但种植土的Cu含量略大于覆盖原土,Zn含量远大于覆盖原土;(2)植物能富集土壤和垃圾中的重金属,木本植物的根部富集重金属的能力强于草本植物,但重金属在草本植物根、茎、叶中的迁移速度大于木本植物;(3)植物根、茎、叶的Cu、Zn含量均远大于未受污染土壤种植植物相应部位的Cu、Zn含量,种植的植物不能供家养动物食用,以免通过食物链作用危及人体安全.     

龙口市污灌区重金属污染影响因子分析

在龙口市污灌区采集70个土壤样品测定Cr、Ni、Pb、Zn、Cu、Co、As和Cd含量,利用富集因子法分析各重金属的空间分布情况,采用地理探测器模型评估7个影响因子对重金属空间分布的影响及各影响因子间的交互作用.结果表明:(1)Cu、Pb、Zn、As、Cd的富集程度较大,Co、Cr、Ni富集程度较低,8种重金属富集系数...     

浅层地下水重金属元素的富集特征研究

以淮南市浅层地下水为研究对象,采集并测试了130个水样中Fe、Mn、Cu、Zn、Pb、Cd和M等元素的含量及相关指标.通过分析pH与重金属的相关性,得出了重金属在水中的富集特征,即VFe＞VCu＞VZn＞VPb＞VMn.利用主成分对7种重金属进行分类并分析其富集成因,最后将测试结果与土壤重金属含量相比较,确定了重金属元...     

淮南潘集矿区农田土壤重金属污染特征及在小麦中累积特征研究

为探究淮南潘集矿区内农田土壤和小麦中重金属的污染状况,选取了16块研究样地,测定其农田土壤和小麦不同部位中Cu、Zn、Pb、Cd、As含量,利用生物富集系数(BCF)和转运系数(TCF)分析重金属在小麦中的迁运行为,并进行重金属化学形态分析和潜在生态风险指数分析。结果表明,矿区农田土壤Zn、Pb浓度平均值低于背景浓度,Cu、Cd、As浓度平均值分别是背景浓度的1.03、4.17、1.81倍。5种重金属的化学形态以残渣态为主,Cu、Zn、Pb、Cd、As的残渣态质量分数平均值分别为47.44%、50.33%、43.36%、46.84%、98.86%。矿区农田土壤重金属综合潜在生态风险指数处于轻度或中度等级,相对较轻,主要贡献重金属是Cd。Cu、Zn易于富集在小麦地上部分,Pb、Cd、As大部分富聚在地下部分。     

铜绿山矿区菜地土壤重金属污染特征

以铜绿山矿区菜地为研究对象,测定了土壤和蔬菜中Cu、Zn、Pb、Cd 4种重金属的含量,分析了土壤-蔬菜体系重金属的污染特征和蔬菜对重金属的富集能力。结果表明:矿区菜地土壤中重金属Cu、Zn、Pb、Cd的污染因子分别为10.63、1.12、1.10、0.06,表明Cu污染非常严重,Zn、Pb属轻度污染,Cd无污染;参考《食品中污染物限量》(GB 2762—2017)、《食品中铜限量卫生标准》(GB 15199—94)以及《食品中锌限量卫生标准》(GB 13106—91),蔬菜中Cu、Zn污染较严重且具有普遍性;蔬菜中Cd含量虽均未超出食品安全限值,但明显高于蔬菜根部土壤中的Cd含量;叶菜类、根茎类蔬菜中Pb均未超标,瓜果类蔬菜中Pb超标;蔬菜可食部位对重金属的富集能力为CdZnCuPb;蔬菜中重金属含量与土壤重金属含量总体表现出较弱的相关性,表明蔬菜中重金属的积累不完全决定于土壤重金属的含量,还与土壤中重金属的生物有效性、环境行为及其他环境因素有关。     

雷州半岛土壤重金属分布特征及其污染评价

在雷州半岛采集了106个土壤表层样品,分析了其中8种重金属元素(Cu、Pb、Zn、Cr、Ni、Cd、Hg和As)的全量.结果表明,雷州半岛土壤重金属污染由高到低排序为Ni＞Cr＞Hg＞Cu＞Zn＞Cd＞As＞Pb,Zn、Cd、As和Pb质量浓度均没有超标,Hg和Cu质量浓度超标率亦不高,但Ni和Cr平均质量浓度达49.81、87.13 mg/kg,高于国内外其他对照区域,超标率分别为25.47%和24.53%;重金属元素在雷州半岛各土壤利用类型中分布规律不明显,按4种主要土壤利用类型受重金属污染程度大小排序为甘蔗地＞果园土＞水田＞菜地;雷州半岛土壤综合污染指数总平均为0.970,土壤总体上尚清洁,重金属污染处于警戒水平;雷州半岛各区域中,徐闻、雷州两地土壤重金属质量浓度明显高于其他地区,其主要原因是徐闻、雷州两地成土母质主要为玄武岩,造成土壤Cr、Ni及其他重金属背景值较高.     

浙江省铅锌矿区土壤重金属污染及重金属超富集植物筛选

分别以浙江省境内富阳某铅锌矿区(FY)、淳安某铅锌矿区(CA)、诸暨某铅锌矿区(ZJ)和三门某铅锌矿区(SM)为研究对象,对铅锌矿区土壤的Zn、Pb、Cu、Cd 4种重金属污染状况及其上生长的16种优势草本植物的重金属富集特征进行了研究。结果表明,FY、ZJ和SM的土壤均受Cd、Zn、Pb重度污染,而CA的土壤受Cd、Zn、Cu重度污染。4个铅锌矿区的Cd污染最严重,其次为Zn污染。CA的伴矿景天(Sedum plumbizincicola)和ZJ的紫花香薷(Elsholtzia argyi)地上部Cd质量浓度分别为571.2、218.7mg/kg,且富集系数和转运系数均超过1,达到了Cd超富集植物的标准,表明这两种植物均可能是Cd超富集植物。     

煤矿复垦区土壤重金属分布特征与质量评价

为保证煤矿复垦区种植农作物的充填复垦土壤的生态安全,以淮南矿区煤矸石充填复垦地为研究对象,通过对研究区内Cd、Cr、Ni、Pb、Cu、Zn和Hg 7种重金属不同深度含量分析,总结其纵向分布特征,并将研究区土壤重金属含量与淮南市土壤背景值、《土壤环境质量标准》(GB 15618-1995)作比较,分析这7种重金属的污染程度.结果表明,这7种重金属都有不同程度的污染,其中土壤受Cd污染最严重,土壤中重金属垂直方向上无确定分布规律.总体而言,土壤重金属潜在生态风险属于强生态危害.从垂直方向来看,重金属潜在生态风险指数(RD随着深度的增加出现先下降后升高的趋势,其中40～60 cm深度的RI最大.重金属生态危害程度依次为Cd＞ Hg＞ Ni＞ Cu＞ Cr＞ Pb＞ Zn,其中Cd为矿区土壤中最主要的重金属污染生态风险因子.     

重金属离子在腐植酸上吸附的研究

对4种代表性重金属离子在腐植酸上吸附、pH对竞争吸附的影响及其吸附机理进行了研究。结果表明，Cu2＋、Pb2＋、Zn2＋的吸附等温线为F型，而Cd2＋等温线为L型；2．5＜pH＜3．5时，竞争吸咐次序为Cu2＋＞Pb2＋＞Cd2＋＞Zn2＋；pH＞5．0时，Cd2＋＞Cu2＋＞Zn2＋＞Pb2＋；Cu2＋在腐植酸上的吸附主要是以与腐植酸形成配合物的方式相互结合。     

乙二胺二琥珀酸和柠檬酸对黑土中外源重金属的活化效应

通过解吸实验和小麦盆栽实验,研究了生物可降解有机配体乙二胺二琥珀酸(EDDS)、柠檬酸(CIT)对黑土中外源Cu、Cd、Zn和Pb的活化效应.不同浓度EDDS﹑CIT对黑土中外源重金属解吸实验表明,EDDS对黑土中外源Cu、Cd、Zn和Pb的解吸远高于CIT.重金属/EDDS摩尔比为1∶1时,4种重金属的解吸率在50.8%～69.2%.小麦盆栽实验表明,EDDS为5 mmol/kg时,对小麦幼苗茎叶和根系中重金属含量影响较大,明显导致小麦幼苗茎叶和根系中Cd、Cu、Pb和Zn的富集量增加.EDDS处理组Cd、Cu、Pb和Zn的茎叶富集系数远高于对照组和CIT处理组.随时间的增加,EDDS处理组和CIT处理组重金属的根系富集量均增加,但对照组和CIT处理组大部分重金属14 d茎叶富集量略低于7 d茎叶富集量.因此,EDDS对黑土中外源重金属有较强的解吸和活化能力,可以较大程度地强化小麦幼苗根系对黑土中外源Cd、Cu、Pb和Zn的吸收并诱导这些重金属由根系向茎叶迁移.     

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。     

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.     

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.     

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.     

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。     

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.     

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.     

Sources and fate of PCDD and PCDF

PCDD and PCDF were found in urban air particulates from St. Louis and Washington, D.C., and in sediments from the Great Lakes and Siskiwit Lake, Isle Royale. The similarity between the PCDD and PCDF found in air particulates and sediment samples and the presence of PCDD and PCDF in sediment from Siskiwit Lake (a location which can receive only atmospheric inputs) suggest that these compounds are emitted to the atmosphere from combustion sources. The historical input of PCDD and PCDF to dated sediment cores shows a strong increase since 1940, and this suggests that the incineration of chlorinated organic compounds is an important source of PCDD and PCDF to the environment.