模拟酸雨条件下降尘中Cu,Pb,Zn,Cr各形态的溶出和转化研究

本文用Ｔｅｓｓｌｅｒ方法，研究了模拟酸雨条件下，降尘中Ｃｕ，Ｐｂ，Ｚｎ，Ｃｒ各形态的溶出和相互转化。试验表明：（１）降尘中Ｃｕ，Ｃｒ的溶出量随酸雨酸度的增大而增加；Ｐｂ，Ｚｎ没分别在ＰＨ＝３．５和ＰＨ＝４．５时溶出量最大，溶出的金属多源于可交换态和碳酸盐结合态，说明这两种形态的稳定性较差。（２）在模拟酸雨条件下，Ｃｕ，Ｐｂ，Ｚｎ，Ｃｒ各形态的含量发生了较大变化；Ｃｕ从其优势形态有机结合态向可交换态     

风浪扰动对太湖水体重金属形态的影响

对不同风浪条件下水体中的悬浮颗粒物,采用ICP-AES测定其中Co,Cr,Cu,Ni,Pb,Zn,Al,Fe和Mn不同形态的含量.研究表明,水体中Al,Fe,Co,Cr,Pb和Ni可提取态含量随风浪扰动程度的增强其含量均有不同程度的增大. Mn,Zn和Cu在7m·s-1风浪下含量最高,11m·s-1风浪次之,2m·s-1风浪最小.7m·s-1风浪与2m·s-1风浪相比,水体中Mn, Co, Cr, Zn, Cu和Ni的B1, B2, B3态含量增加3-20倍.11m·s-1风浪与7m·s-1风浪相比,Co, Cr和Ni的B1态含量分别增加31.1%-76.8%,Mn, Zn和Cu分别减少22.1%-38.6%; Cr,Zn和Ni的B2态含量增加12.1%-50.2%, Mn减少65.6%, Co和Cu的含量相当; Co和Ni的B3态含量增加15.4%-10.3%,Cr,Mn,Zn和Cu略微减少.水体中的金属主要以Fe-Mn氧化物结合态存在,且金属的三态比例随风浪的变化不明显. Mn的生物有效性最高,Zn,Cu和Ni次之,毒性较大的Pb和Cr的生物有效性较低.Al, Fe和Pb的Fe-Mn氧化物结合态比例非常高,约有74.56%-100%. Co,Cr和Ni的有机结合态比例较高,且Co和 Ni的三态比例比较均一,Cu的B3态较低.     

铜陵矿区土壤中镉存在形态及生物有效性

采取Tessier连续提取法，研究铜陵矿区不同功能区表层土壤中镉的化学形态分布和生物有效性。结果表明，各种土壤中的镉含量全部高于地区背景值，主要来源与矿业活动有关，部分样品还有矿体的风化富集叠加，土壤镉污染指数PCd为1．15～79。镉含量依次为矿体风化土壤→废矿堆下垫土→市郊菜地土→矿区铜草土、路边土和稻田土→其它土壤。其形态分布，酸性土壤中以Fe-Mn氧化态和可交换态为主，其余三态相对较低；碱性土壤中有机态和残渣态比例较高，碳酸盐态和可交换态所占的比例低。土壤中生物可利用态镉的含量较高，占土壤总镉的60．20%-98．3％，生物不可利用态仅占1．7％-39．2％。     

An Operationally Defined Method to Determine the Speciation of Mercury

This paper presents a modified method of an operationally determined speciation of mercury in soil. The analytical work was mainly concerned to suit properly with inductively coupled plasma-atomic emission spectrometry (ICP-AES). Soil samples analysed in this study were selected from open areas around a crematorium, a waste incinerator, and two power plants. Results show that both topsoil and subsoil samples were dominated by elemental mercury Hg(0) and mercuric sulphide (HgS). The significant correlation between sulphur concentration and HgS was found in topsoil samples.     

外加镍在土壤中的形态与再分配

镍处理土壤经室内培养12周后,采用连续提取技术对试验土壤中镍的形态与再分配方式进行了研究。研究结果表明,外加的水溶性镍进入土壤后的主要存在形态与添加的剂量有关:低剂量时,以铁锰氧化态为主,这一形态在100mg·kg-1处理土壤中占比例最大,达到31.6%;高剂量时,以交换态为主,这一形态在1600mg·kg-1处理土壤中占比例最大,达到48.4%。随着镍添加剂量由0(对照)增加到1600mg·kg-1,再分配系数逐渐由1.00增大到30.65;金属结合强度系数则由0.90减小至0.25,也反映出进入土壤中镍的剂量较大时,镍是以不稳定的形态占优。试验结果也证实了土壤具有减小镍的环境危害的作用,但这种缓冲能力是有限的。随着时间的推移,镍的形态会继续发生变化,但这一转化过程是缓慢的。因此,一旦土壤发生重金属污染,其对土壤环境的影响将是长期的。     

Speciation and fractionation of heavy metals in soil experimentally contaminated with Pb,Cd, Cu and Zn together and effects on soil negative surface charge

Speciation and fractionation of heavy metals in soil subsamples experimentally loaded with Pb, Cd, Cu and Zn in orthogonal design was investigated by sequential extraction, and operationally defined as water-soluble and exchangeable(SE), weakly specific adsorbed( WSA),Fe and Mn oxides-bound(OX) and organic-bound( ORG). The results showed that fractions of heavy metals in the soil subsamples depended on their speciation. About 90% of Cd and 75% of Zn existed in soil subsamples in the SE fraction. Lead and Cu existed in soil subsamples as SE, WSA and OX fractions simultaneously, although SE was still the major fraction. Organic-bound heavy metals were not clearly apparent in all the soil subsamples. The concentration of some heavy metal fractions in soil subsamples showed the good correlation with ionic impulsion of soil, especially for the SE fraction. Continuous saturation of soil subsamples with 0.20 mol/L NH4CI, which is the first step for determination of the negative surface charge of soil by the ion retention method, resulted in desorption of certain heavy metals from the soil. It was found that the percentage desorption of heavy metals from soil subsamples depended greatly on pH, the composition and original heavy metal content of the soil subsamples. However, most of the heavy metals in the soil subsamples were still be retained after multiple saturation. Compared with the parent soil, the negative surface charge of soil subsamples loaded with heavy metals did not show difference significantly from that of the parent one by statistical analysis. Heavy metals existed in the soil subsamples mainly as exchangeable and precipitated simultaneously.     

湘江水体中重金属的化学形态及分布特征的研究

水体中重金属的生态效应和迁移转化规律与其化学形态密切相关。本文结合湘江重金属水容量与背景值的研究,较系统地研究了铜、铅、镉和锌的化学形态及其在全江段水中的分布特征。应用阳极溶出伏安法,得到湘江水中重金属总量、溶解态含量和悬浮态含量的分配与分布特征,还有溶解态所包含的金属的主要存在形态及与之共存的其它多种形态(包括悬浮态)共十种,该文对其形成、分配和相互转化进行了综合分析。     

聚合铝混凝过程研究:不同形态硅酸的影响作用

研究了不同形态硅酸对聚合铝混凝过程的影响作用 .实验结果表明经预制形成的具有不同形态分布组成的硅酸与聚合铝 ,在投加后相互间发生了十分复杂的物理化学作用 ,并受溶液pH值的影响 ,从而最终决定了混凝效果 .反应过程中所生成的形态产物及其物化特征 ,很大程度上取决于聚合铝碱化度以及所投加的Si Al比 .其中碱化度越高 ,最终产物所带电荷越高 .而不同硅酸所起影响作用分别取决于聚合程度 ,在与聚合铝反应过程中表现出一定的规律性 .单体硅酸与单体铝迅速发生较强的络合作用 ,抑制了多聚水解铝阳离子的形成 .聚合硅酸则倾向于与聚合铝形态相互作用形成一定的胶状化合物 ,从而在溶液中稳定存在 .对于胶体硅酸 ,在聚合铝作用下迅速凝聚形成更大的聚集体 ,在颗粒物间架桥形成粗大的絮体 .所得结果对混凝机理的解释与复合混凝剂的发展提供了一定的参考作用     

Investigation of the complexation of metal-ions by strong ligands in fresh and marine water

SCOPE: The detection and investigation of metal ions bound in strong complexes in natural waters is a difficult task, due to low concentration of the metal ions themselves, and also of the strong ligands, which, moreover, are often not of a well-defined composition. Here, a method is proposed for the investigation of the speciation of metal ions in natural waters. OBJECTIVE AND METHOD: It is based on the sorption of metal ions on strongly sorbing ion exchange resins, i.e. complexing resins. For this reason the method is called Resin Titration. It has been shown in previous investigations that the concentration of metal ion totally sorbed by a particular resin, and its reaction coefficient in the solution phase in the presence of the resin, can be determined from the sorption data using a simple relationship. Here, a data treatment (the Ruzic linearization method) is proposed for also determining the concentration of the ligands responsible for the complex in equilibrium with the resin. RESULTS: The method was applied to data obtained by Resin Titration of a freshwater and a seawater. Copper(II) and aluminium(III) were considered, using Chelex 100 as a titrant, due to its strong sorbing properties towards these metal ions. The results were: the total metal concentration in equilibrium with the resin, the side reaction coefficients, and the concentration of ligands. In all these cases the ligands forming very strong complexes were found to be at concentration lower than that of the metals. CONCLUSION: The Ruzic linearization method allows the determination of the concentration of the ligands forming very strong complexes in equilibrium with Chelex 100. The reaction coefficient was better determined by the calculation method previously proposed for RT. The ligands responsible for the strong complexes were found to be at low concentration, often lower than that of the metal ions considered. The metal in the original sample is partly bound to these ligands, since the complexes are very strong. Only a part of the metal is linked to weaker ligands, or free.     

Speciation of heavy metals in estuarine sediments in the northeast of Brazil

An analytical procedure involving a three-step sequential extraction was used to determine the chemical association of heavy metals (Zn, Cr, Mn and Fe) with the major phases (exchangable, reducible and oxidizable) in samples from a fishpond of estuarine sediments. The pond is located in the Capibaribe River estuary, within the boundaries of the city of Recife, in the State of Pernambuco in the northeast of Brazil. The total metal content was determined as well. All metals were extracted from the residual fraction at a percentage greater than 50%.