宝鸡城市土壤重金属生物活性与环境风险

在野外调查与前期研究的基础上,根据一点多样混合采样法收集宝鸡市工业区土壤分析样品50个,采用Tessier连续形态分析法对城市土壤重金属Pb、Zn、Cd、Cr、Cu、Sb形态进行分级并使用ICP-OES对其各形态含量进行测定.在对6种重金属活性系数(MF)、迁移系数(MJ)、综合潜在生态风险指数(RI)及人群健康风险研究的基础上,对重金属地球化学形态分布、迁移能力、生物活性与环境风险进行了探讨.结果表明,宝鸡工业区城市土壤重金属Zn、Cd、Cr、Cu、Sb形态均以残渣态为主,而Pb主要以铁锰氧化物结合态为主;在各形态含量所占百分比中,重金属Cr可交换态含量最低.化学形态分析结果显示,6种重金属整体迁移的顺序为:Pb(77.60%)Zn(47.36%)Cu(35.86%)Cd(30.91%)Sb(16.46%)Cr(11.31%);土壤Pb(MF=35.77%)的生物活性最强,Cd(MJ=0.091)的迁移能力最大.城市土壤重金属Cd和Cr对儿童和成人的致癌风险处于中低等水平,但Cr对儿童将产生较大的非致癌风险.而重金属Pb对儿童和成人均产生非常明显的非致癌风险和中等程度的致癌风险,可见,重金属Pb是宝鸡市城市土壤最主要的环境污染物与健康风险因子.重金属Pb、Zn、Cd、Cr、Cu、Sb工业排放与化石燃料燃烧的来源和城市儿童高铅血症的检出率说明宝鸡工业区重金属的干湿尘降污染应该引起高度重视.     

西安城区地表灰尘中重金属分布、来源及潜在生态风险

以西安城区为研究区域,采集58个地表灰尘样品,测定了地表灰尘中重金属As、Co、Cr、Cu、Mn、Ni、Pb和Zn的含量。西安城区地表灰尘中除As(9.8 mg/kg)和Mn(417.0 mg/kg)外,其余各元素含量(Co、Cr、Cu、Ni、Pb和Zn平均含量分别为12.6、213.0、59.4、48.7、145.4和234.2 mg/kg)均高于陕西省土壤元素背景值。Arc GIS空间插值分析表明As、Co、Cr、Pb、Mn和Ni主要在西郊和主城区富集,Cr主要累积在东郊以及北郊部分地区,Zn则在二环与主城区之间富集明显。多元统计分析结果显示地表灰尘中Co、Cu、Mn、Ni和Cr主要受工业活动影响,As、Pb和Zn主要来源于汽车尾气排放和商业活动等。利用Hakanson潜在生态风险指数研究重金属生态风险。重金属总的生态风险水平达到强度,Pb处于较强生态危害水平,Cu属中等生态危害程度,As、Co、Cr、Mn、Ni和Zn均为轻微生态危害。     

武汉集中式饮用水源地土壤重金属的时空分布特征及生态风险评价

研究了武汉市19个集中式饮用水源地土壤重金属Cd、Hg、As、Pb、Cr、Cu、Ni和Zn的时空分布特征,采用单因子污染指数和综合污染指数分析重金属污染程度,利用潜在生态风险指数评价重金属生态风险,通过相关性和聚类分析重金属的来源.结果表明,武汉市中心城区水源地土壤重金属的含量普遍高于远城区,同时长江干流附近的水源地土壤重金属含量普遍高于长江支流.Hg、As、Pb、Cr、Cu、Ni和Zn的单项潜在生态风险指数平均值均小于40,属于轻微风险程度.Cd的单项潜在生态风险指数平均值在80~160范围内,属于强度风险程度.武汉集中式饮用水源地土壤重金属的综合潜在生态风险指数平均值为142.12,属于轻微风险水平.相关性分析表明,武汉集中式水源地土壤重金属Cu、Pb和Cr来源相似,均与交通有关;Ni、As、Cr和Cu来源相似,均与冶金生产有关;Zn、Hg和Cr来源相似,均与防腐和催化化工有关.武汉白沙洲水厂和堤角水厂周边土壤长期定点监测表明,2017年后武汉集中式水源地土壤各种重金属含量均呈现显著下降趋势,其生态风险在未来将进一步降低.     

铜陵市惠溪河滨岸带土壤重金属形态分布及风险评估

为揭示惠溪河滨岸带土壤重金属(Pb、Cu、Zn、Ni、Cr、Cd和As)形态分布和生态风险状况,沿河采集12个采样点的土壤样品,采用改进的Tessier五步连续提取法开展形态分析,并以Hkanson潜在生态危害指数法进行生态风险评估. 结果表明:①As和Cr以残渣态占绝对优势,Zn、Pb和Ni以残渣态和Fe-Mn氧化物结合态为主,Cu则以残渣态和有机结合态为主,Cd具有形态多样的分布特征;②7种重金属污染程度排序为As＞Cd＞Zn＞Cu＞Pb＞Ni＞Cr,潜在生态风险大小排序为Cd＞As＞Cu＞Pb＞Ni＞Zn＞Cr,其中Cd和As属极高风险等级,Cu为中等风险等级,其他4种元素则为轻微风险等级;③根据潜在生态风险指数,小倪村、狼尾湖右岸和大倪村采样点属于高风险等级,其他9个采样点均属于很高风险等级;④由综合污染及潜在生态风险贡献率水平,初步判定As和Cd为惠溪河滨岸土壤重金属污染治理和修复的优先控制对象.      

滇黔桂岩溶区河漫滩土壤重金属含量、来源及潜在生态风险

利用全国地球化学基准计划在滇黔桂岩溶区35个点位采集的70件河漫滩表、深层土壤样品,分析了As、Cd、Cr、Cu、Hg、Ni、Pb和Zn 8种重金属元素含量特征,探究了重金属来源、污染状况及潜在生态风险.结果表明,8种重金属元素含量大部分均高于全国土壤背景值,在滇东南地区含量最高,桂西北地区最低.表层土壤Cd、Hg明显富集,As、Cr、Cu、Ni与深层土壤含量相当;As、Cd、Hg、Pb、Zn在农田、菜地中明显高于深层土壤,Cr、Cu和Ni在各类土地中与深层土壤相当.因子分析结果显示,表层土壤中Cd、Cr、Cu、Ni受地质背景控制,As、Pb、Zn既与地质背景有关,也受人为活动影响,Hg受人为活动影响较严重;深层土壤中Cd、Cr、Cu、Ni、Cr、Zn继承了区域母岩特征,As、Hg和Pb受地质背景和人为活动双重影响.地累积指数法和富集因子法污染评价结果表明,研究区河漫滩表层土壤中Cd、Hg污染较重,As、Cr、Cu、Ni、Pb、Zn大部分为轻度污染或无污染.各重金属潜在生态风险指数高低顺序依次为Hg > Cd > As > Cu > Ni > Pb > Cr > Zn,Cd和Hg的生态风险指数之和占综合指数的82.43%,生态风险最高;滇东南地区重金属潜在风险综合指数最高,具重度生态风险.     

新疆和硕绿洲农田土壤重金属污染及生态风险

新疆和硕绿洲采集82个耕地土壤样品,测定其中As、Cd、Cr、Cu、Mn、Ni、Pb和Zn等8种重金属元素的含量。采用地统计法、污染负荷指数(PLI)和潜在生态风险指数(RI)评估农田土壤重金属污染和潜在生态风险,并讨论重金属主要来源。结果表明:(1)和硕绿洲农田土壤所有重金属元素含量平均值均未超出国家二级标准的限值,Cd、Cr、Ni、Pb和Zn含量的平均值分别超出新疆灌耕土背景值的2.0、1.51、1.18、2.13和8.47倍。(2)农田土壤Cd与Zn呈现中度污染,Cr、Cu、Ni和Pb轻度污染,Mn轻微污染,As无污染。研究区PLI平均值呈现轻度污染。(3)各重金属元素单项生态风险指数从大到小依次为:Cd、Ni、As、Cu、Cr、Zn与Pb。农田RI平均值属于轻微生态风险。重金属元素含量、污染与生态风险空间分布格局各不相同。(4)和硕绿洲农田土壤As、Pb和Zn主要受到人为因素的影响,Cr、Cu、Mn和Ni主要受到土壤地球化学作用的影响,Cd受人为污染和自然因素共同影响。Cd是研究区农田土壤主要的污染因子之一,对农田土壤污染及潜在生态风险的贡献较大,农田土壤Cd污染值得关注。     

宿南矿区土壤重金属含量特征及其来源解析

为研究淮北煤田宿南矿区土壤重金属含量特征,测试了土壤中重金属Fe、Mn、Cd、Cr、Pb、Ni、Zn和Cu的含量,采用地累积污染指数法和潜在生态风险指数法对土壤重金属污染进行评价,并运用多元统计分析对重金属污染来源进行解析。结果表明,Cd、Cr、Pb、Ni、Zn和Cu的均值含量不超过土壤环境质量二级标准;综合评价结果显示,Cd污染累积程度明显,且Cd是最主要的生态风险因子;聚类分析将重金属划分为具有相似地球化学过程的3组,即Ⅰ类(Fe、Ni和Pb)、Ⅱ类(Mn、Cu和Cd)和Ⅲ类(Zn和Cr);主成分分析从重金属元素中筛选出3个主成分(PC1、PC2和PC3),PC1(Mn、Cu和Cd)表示为煤矿开采与道路煤尘扩散污染,PC2(Fe、Ni和Pb)解析为土壤母质与尾气排放作用,PC3(Zn和Cr)表示交通运输与农业生产活动污染。     

锰矿区周边农田土壤重金属污染特征、来源解析及风险评价

为了解锰矿周边农田土壤重金属污染和生态风险情况,采集某矿区周边174份农田土壤样品,分析了土壤中8种重金属(Cu、 Zn、 Pb、 Cr、 Ni、 Mn、 As和Hg)的含量,采用主成分分析(PCA)和正定矩阵因子分解模型(PMF)分析土壤重金属的来源,通过单因子污染指数法、地累积指数法、潜在生态风险指数法和人体健康风险评价模型评价土壤重金属生态环境风险.结果表明,研究区农田土壤Cu、 Zn、 Cr、 Ni、 Mn和Hg含量的均值均高于贵州省土壤背景值,100%样本Zn和38.86%样本Cu均超过农用地土壤污染风险筛选值.源解析显示农田土壤重金属的主要来源为矿业开采排放源,其次为农业活动和交通运输混合源、自然源和农业活动源.风险评价结果表明,土壤中Ni、 Cr、 Pb和As属于清洁水平,Hg和Cu属于轻度污染水平,Zn属于偏中度污染水平,Mn属于偏重污染水平.Cu、 Zn、 Pb、 Cr、 Ni、 Mn和As存在轻微潜在生态风险,Hg存在强潜在生态风险.研究区整体存在强潜在生态风险,8种重金属存在致癌风险和0～5岁儿童非致癌风险,主要贡献因子分别是Cr和Mn.     

万庄金矿田土壤重金属的垂直分布及形态研究

利用等离子体发射光谱法、原子荧光光谱法等研究了北京水源涵养区上游万庄金矿田4个土壤剖面样品中的Cu、Zn、Ni、Pb、Cd、Cr、Hg和As共8种重金属元素在剖面上的分布特征,以及Cu、Zn、Pb、Cd、Cr、Ni元素的形态分布特征,并对重金属元素污染现状进行了评价。结果表明部分重金属元素在土壤表层有明显的富集现象,Cd、As、Pb、Zn、Cu、Hg 6种重金属基本都随深度的增加,含量大体呈现逐渐减小的趋势,Cr、Ni有较相似的迁移和富集规律;相关性分析发现Zn、Ni、Cd、Cr、和As的相关性显著可能具有同源性。形态分析可知重金属Zn、Cd的迁移能力相对较高。地累积指数评价结果可见,土壤中Pb、As、Cd环境生态污染较严重。     

喀斯特高原石漠化治理示范区土壤和农作物重金属含量特征

通过采集贵州毕节撒拉溪石漠化治理示范区土壤和主要农作物样品,分析了土壤和农作物样品中重金属Cr,Co,Cu,Cd, Pb,Zn,As和Ni含量,采用富集因子评价了土壤中重金属的污染状况,并分别采用潜在生态风险指数(RI)和生物富集系数评价了示范区土壤重金属的潜在生态风险和农作物对重金属的富集特征.结果表明,示范区土壤中Cr,Co,Cu,Cd,Pb, Zn,As和Ni平均含量分别为123,28.0,67.8,1.52,32.7,132,25.6和56.5mg/kg,除Cd外,其他均低于农用地土壤污染风险筛选值;其中森林土重金属污染程度的评价等级均为无污染-轻度污染,旱地土中Cd和Cu个别样点存在中度污染,其他均为无污染-轻度污染.潜在生态风险评价结果表明,示范区土壤重金属Cr,Co,Cu,Pb,Zn,As和Ni的单项潜在危害指数分别为1.23,4.67,3.39, 1.36, 0.53,8.54和2.83,潜在危害等级均为轻微生态危害,Cd的单项潜在危害等级为中等生态危害,8种重金属的综合生态危害等级为轻微生态危害.Cd在土豆中的生物富集系数为4.05,其他重金属的富集系数均小于2.不同农作物对土壤中不同重金属的富集能力有较大差异,其中Cd,Zn,Co,Cu, Pb和Ni在土壤-土豆系统中的迁移富集能力相对较高,Cr和As在土壤-玉米系统中的迁移富集能力相对较高,其他农作物对重金属的迁移富集能力较弱.     

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.     

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.     

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.     

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.     

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.     

Effects of chitosan on growth of an aquatic plant (Hydrilla verticillata) in polluted waters with different chemical oxygen demands

Effects of chitosan on a submersed plant, Hydrilla verticillata, were investigated. Results indicated that H. venicillata could prevent ultrastructure phytotoxicities and oxidativereaction from polluted water with high chemical oxygen demand (COD). Superoxide dismutase (SOD) activity and malondialdehyde (MDA) contents in H. verticillata treated with 0.1% chitosan in wastewater increased with high COD (980 mg/L) and decreased with low COD (63 mg/L), respectively. Ultrastructural analysis showed that the stroma and grana of chloroplast basically remained normal. However, plant cells from the control experiment (untreated with chitosan) were vacuolated and the cell interval increased. The relict of protoplast moved to the center, with cells tending to disjoint. Our findings indicate that wastewater with high COD concentration can cause a substantial damage to submersed plant, nevertheless, chitosan probably could alleviate the membrane lipid peroxidization and ultrastructure phytotoxicities, and protect plant cells from stress of high COD concentration polluted water.     

Removal of cadmium using MnO2 loaded D301 resin

MnO2 loaded weak basic anion exchange resin D301 （Anion exchange resin, macroreticular weak basic styrene） as adsorbent has been prepared and applied to the removal of cadmium. The adsorption characteristics have been investigated with respect to effect of pH, equilibrium isotherms, removal kinetic data, and interference of the coexisting ions. The results indicated that the Cd^2＋ could be efficiently removed using MnO2 loaded D301 resin in the pH range of 3-8 from aqueous solutions with the co-existence of high concentration of alkali and alkaline-earth metals ions. The saturate adsorption capacity of the Cd^2＋ was 77.88 mg/g. The adsorption process followed the pseudo first-order kinetics. The equilibrium data obtained in this study accorded excellently with the Langmuir adsorption isotherm.     

Effect of coagulation pretreatment on the fouling of ultrafiltration membrane

The purpose of this study is to understand the effect and mechanism of preventing membrane fouling, by coagulation pretreatment, in terms of fractional component and molecular weight of natural organic matter （NOM）. A relatively higher molecular weight （MW） of hydrophobic compounds was responsible for a rapid decline in the ultrafiltration flux. Coagulation could effectively remove the hydrophobic organics, resulting in the increase of flux. It was found that a lower MW of neutral hydrophilic compounds, which could remove inadequately by coagulation, was responsible for the slow declining flux. The fluxes in the filtration of coagulated water and supernatant water were compared and the results showed that a lower MW of neutral hydrophilic compounds remained in the supernatant water after coagulation could be rejected by a membrane, resulting in fouling. It was also found that the coagulated flocs could absorb neutral hydrophilic compounds effectively. Therefore, with the coagulated flocs formed on the membrane surface, the flux decline could be improved.     

Penetration analysis of elements and bioleaching treatment of spent refractory for recycling

Acidithiobacillus ferrooxidans ATCC23270 and Acidithiobacillus thiooxidans TM-32 were used for bioleaching of spent refractories of aluminium and copper melting furnaces for their recycling.Firstly,penetration of elements into aluminium melting furnace refractory was investigated and it was found that up to 7 cm from surface was contaminated.Comparison on leaching efficiency by the strains ATCC23270 and TM-32 found that the strain ATCC23270 could treat larger amount of the refractories than the strain TM-32 could do.In the experiment of bioleaching of spent refractory aluminium melting furnace by the strain ATCC23270,high leaching efficiency were obtained on Al,Si,and Ca,and extremely low leaching performance was,however,shown on the rest of elements i.e.,Na,Mn,and Zn.Under the strain TM-32 use,relatively high leaching performance was recognized on Al,Si,Ca,Na,Mn,and Zn.In the experiment of bioleaching for spent refractory copper melting furnace,almost the same leaching trends were shown on Cu,Zn,Al,and Si under the strains ACTT23270 and TM-32 uses.     

Simultaneous removal of ammonium and phosphate by zeolite synthesized from coal fly ash as influenced by acid treatment

Zeolite synthesized from fly ash （ZFA） without modification is not efficient for the purification of NH4＋ and phosphate at low concentrations that occur in real effluents, despite the high potential removal capacity. To develop an effective technique to enhance the removal efficiency of ammonium and phosphate at low concentrations, ZFA was modified with acid treatment and the simultaneous removal of ammonium and phosphate in a wide range of concentration was investigated. It was seen that when compared with untreated ZFA, only the treatment by 0.01 mol/L of H2SO4 significantly improved the removal efficiency of ammonium at low initial concentrations. The behavior was well explained by the pH effect. Treatment by more concentrated H2SO4 led to the deterioration of the ZFA structure and a decrease in the cation exchange capacity. Treatment by 0.01 mol/L H2SO4 improved the removal efficiency of phosphate by ZFA at all initial P concentrations, while the treatment by concentrated H2SO4 （≥0.9 mol/L） resulted in a limited maximum phosphate immobilization capacity （PIC）. It was concluded that through a previous mild acid treatment （e.g. 0.01 mol/L of H2SO4）, ZFA can be used in the simultaneous removal of NH4＋ and P at low concentrations simulating real effluent.