太湖浮游植物中重金属含量的季节变化特征及湖区差异

近年来随着社会经济的发展,排入太湖的污水中重金属含量不断增加,为研究太湖浮游植物中重金属的污染状况,分别于2009年春季(4月)、夏季(7月)和冬季(12月)对太湖不同湖区展开调查,通过HCA聚类分析和Pearson相关分析探讨不同湖区浮游植物中重金属含量的季节变化,并与优势藻种进行CCA分析,对浮游植物重金属与各藻种关系进行初步探讨.结果表明:太湖浮游植物中重金属的含量大小为:ZnMnPbCuNiCrAsCdHg,其中Zn、Cu、Mn、Pb、Ni的季节变化明显,Zn和Cu、Pb、Ni、Cr之间的相关系数很高且具有同源性.通过对比不同湖区,发现北部梅梁湾的浮游植物重金属含量较高,东太湖和湖心区含量均低于沿岸湖区.CCA分析表明春季重金属与优势藻种呈正相关,而夏季和冬季二者呈负相关.三季中重金属与蓝藻和绿藻的相关性最高,与隐藻的相关性最低.蓝藻中,重金属与铜绿微囊藻的相关性高于水华微囊藻.     

被污染土壤的植物修复研究

植物修复是利用植物吸收、降解、挥发、根滤、稳定、泵吸等作用机理,达到去除土壤、水体中污染物,或使污染物固定以减轻其危害性,或使污染物转化为毒性较低化学形态的现场治理技术.植物修复对于重金属污染土壤的治理修复具有重要意义.已有研究在累积与超累积植物的寻找筛选、植物对重金属等有害物的耐毒和解毒机理、植物修复现场环境调控及根际处理技术等方面取得了大量成果.现代分子生物学、基因工程技术发展有可能使植物修复技术取得重大突破.     

平阴县土壤中重金属元素异常成因研究

通过对平阴县周边及其西部农田区采样调查,平阴县周边元素异常具有异常衬度较高,富集系数大等特征,西部农田区异常具有各元素套合关系好,多数异常衬度不高,富集系数小的特点。结果表明,西部农田区异常是以As,Cd为主要成分的异常,元素含量与SiO2,Al2O3,Fe2O3等常量组分间具有显著的相关性,随SiO2含量的增加而降低,随Al2O3,Fe2O3含量的增加而增加,说明土壤常量组分及其所决定的土壤质地是导致异常形成的主要因素;而平阴城区异常是以S,Hg,As,Zn,Mn等元素为主的异常,是典型的人为综合因素（化工烟尘、工厂污水、生活垃圾）产生的异常。     

辽河油田稠油中贵金属分布和赋存状态研究

以辽河油田稠油为研究对象,通过原子吸收光谱、实沸点蒸馏等手段,研究了辽河油田稠油中Au、Ag、Pt和Pb等贵金属在不同馏分中的分布特征.结果表明,经过实沸点蒸馏后,贵金属不同沸程温度的原油馏分中含量和分布存在很大差异,Au、Ag、Pt、Pd主要集中在渣油馏分中,在沸点》508℃的渣油馏分中Au、Ag、Pt、Pd的比例分别是93.4%、76.9%、73.4%和68.0%;采用选择性萃取的方法对金在稠油中的存在形态的初步研究发现,金在稠油中主要以有机配合物和少量无机配合物形式存在.     

内江市双桥乡土壤重金属含量及风险评价

以四川省内江市双桥乡为研究区域,调查分析各类土壤中重金属（Cu、Pb、Zn、Cd、Cr、As、Hg、Ni）含量情况。采用单因子污染指数、内梅罗综合污染指数和富集因子评价方法,对土壤重金属污染状况进行评价。研究结果表明,该地区Cd、Cr、Cu、Ni、Pb、Zn元素平均含量高于成都经济区、四川省、中国土壤背景值,有一定程度的Cd、Cr、Cu、Ni、Pb、Zn富集,Hg元素有个别样点含量偏高,并且单因子重金属的污染程度依次为：Cd〉Ni〉Zn〉Cu〉Cr〉Pb〉As〉Hg,Cd在绝大部份区域存在轻微污染,由内梅罗污染指数和富集因子评价得出区域综合污染程度为轻度。     

柱撑蛭石吸附去除废水中重金属离子的实验研究

分别利用有机柱化剂十二烷基磺酸钠(SDS)和无机柱化剂聚羟基铝(HA)对蛭石进行柱撑制得十二烷基磺酸钠柱撑蛭石(SDS-V erm icu lite)和聚羟基铝柱撑蛭石(HA-V erm icu lite),并通过XRD、红外光谱、ZETA电位等表征手段对柱撑蛭石进行表征,同时针对柱撑蛭石对Cu2 ,Cd2 ,C r3 3种重金属离子的吸附进行研究,结果表明:吸附去除率受反应时间、重金属离子的初始浓度、pH值等因素的影响,经柱撑后的蛭石对重金属离子吸附的吸附性能比蛭石原矿要强。柱撑蛭石吸附3种重金属离子的动力学吸附过程可用E lov icb方程和双常数方程进行较好的拟合。     

Sediment contamination in floodplains and alluvial terraces as an historical record of gold exploitation in the Carmo River basin,Southeast Quadrilátero Ferrífero,Minas Gerais,Brazil

This paper describes the geochemistry of sediment samples placed in floodplains and alluvial terraces downstream from gold mines in the Carmo River basin, Quadrilátero Ferrífero, Minas Gerais, Brazil. The geochemistry signature Na₂O, K₂O, SiO₂, CaO, MgO, Al₂O₃, Fe₂O₃, TiO₂, P₂O₅, Mn, As, Cu, Zn, Ba, Ni, Cr, S, Co were analyzed in different facies from stratigraphic profiles. As, Cu, Zn, and Mn anomalies are mainly associated with the clayed facies deposited in floodplains and oxbow lakes, and with coarse‐sediment facies deposited in the channel. The facies were accumulated by the gold exploitation activity in the region. The contamination of As, Cu, and Zn was controlled by minerals such as iron oxides and hydroxides (hematite, magnetite, and mainly goethite), manganese oxides, and sulfide‐rich minerals. The As‐bearing sediments of the region characterize one of the most As contaminated area of Brazil. Their main source is associated with gold exploration in the last three centuries.     

固定化海藻吸附金属离子的影响因素

研究了固定化海带吸附含铜、镉溶液过程的影响因素,结果表明,在pH为3.0~5.0时对Cu2+保持高的吸附率,在pH为4.0时对Cd2+的吸附率达到最大.随着Cu2+,Cd2+金属离子初始浓度的降低,吸附率有所降低.对Cd2+的吸附率均随着温度的升高而变大.随着吸附剂浓度的增大,对Cu2+,Cd2+的吸附率逐渐升高,与此相反,对Cu2+,Cd2+的吸附量则逐渐减小.粒径对Cu2+的吸附率影响较小,对Cd2+的吸附率有较明显的变化.     

The Geochemistry of Lake Joyce, McMurdo Dry Valleys, Antarctica

Lake Joyce is one of the least studied lakes of the McMurdo Dry Valleys. Similar to other lakes in this region, Lake Joyce is a closed-basin, permanently ice-covered, meromictic lake. We present here a detailed investigation of major ions, nutrients, and dissolved trace elements for Lake Joyce. Specifically, we investigate the role of iron and manganese oxides and hydrous oxides in trace metal cycling.Lake Joyce is characterized by fresh, oxic waters overlying an anoxic brine, primarily Na–Cl. Surface waters have a maximum nitrate concentration of 26M with a molar dissolved inorganic nitrogen to phosphorus ratio of 477. The supply of nitrogen is attributed to atmospheric deposition, possibly from polar stratospheric clouds. Dissolved phosphorus is scavenged by hydrous iron oxides. The pH is highest (10.15) just beneath the 7-m thick ice cover and decreases to a minimum of 7.29 in the redox transition zone. Dissolved Al exceeds 8M in surface waters, and appears to be controlled by equilibrium with gibbsite. In contrast, concentrations of other trace elements in surface waters are quite low (e.g., 5.4nM Cu, 0.19nM Co, <20pM La). Dissolved Fe, Mn, Ni and Cd were below our detection limits of 13 nM, 1. 8 nM, 4.7 nM and 15pM (respectively) in surface waters. There was a 6-m vertical separation in the onset of Mn and Fe reduction, with dissolved Mn appearing higher in the water column than Fe. Based on thermodynamic calculations, dissolved Mn appears to be controlled by equilibrium with hausmannite (Mn3O4). Co tracks the Mn profile closely, suggesting Co(III) is bound in the lattice of Mn oxides, whereas the Ce profile is similar, yet the Ce anomaly suggests oxidative scavenging of Ce. Release of Cu, Ni, Cd and trivalent REE appears to be controlled by pH-induced desorption from Fe and Mn oxides, although Cu (and perhaps Ni) may be scavenged by organic matter in surface waters.