Metal complexes of crosslinked chitosans Part II. An investigation of their hydrolysis to chitooligosaccharides using chitosanase

This paper investigates the behavior of crosslinked chitosans and metal-complexed crosslinked chitosans under similar hydrolytic conditions. Crosslinked chitosans with trimellitic anhydride, diisocyanatohexane, and dibromodecane as crosslinking agents under heterogenous reaction conditions were used as metal complexing agents by equilibrating them with metal salts such as ZnCl₂, MnSO₄, CuSO₄, CdSO₄, Pb(NO₃)₂, and HgCl₂. Crosslinked chitosan without metal complexation had the same hydrolytic behavior as uncrosslinked chitosan. However, when the crosslinked chitosans were complexed with metals, their rates of hydrolysis and extent of hydrolysis were significantly reduced. Thus, while for chitosan about 840 μg/ml reducing sugar was produced in 4 h time, and 780 μg/ml was produced for diisocyanatohexane crosslinked chitosan, only 400 μg/ml and 320 μg/ml reducing sugars were produced for cadmium sulfate with crosslinked chitosan and diisocyanatohexane crosslinked chitosan, respectively. Similar results are obtained for other crosslinking agents. Studies on preincubation of the metal with the enzyme show that of the metals studied, Mn has no effect on preincubatioin with the enzyme, Hg, Cd, Pb, and Cu completely deactivates the enzyme, while Zn reduces the enzyme activity by about 43.3%. Preincubation of the metal salts with the chitosan shows that Hg and Cu completely deactivate the molecule from enzyme hydrolysis, Cd and Zn inactivate it to the extent of 56.8% and 43.3%, respectively, while Mn has no effect. Availability of the amino functions seems to be a key feature for the chitosanase to hydrolyze the chitosan polymer. This was also proved by the significant increase in the extent of hydrolysis for chitosan samples with 88% (final value 1120 μg/ml reducing sugar) and 85% deacetylation (final value 840 μg/ml reducing sugar). HPIC studies of the products show that a variety of oligomers are produced in the chitosanase enzyme hydrolytic reaction.     

Metal complexes of crosslinked chitosans: Correlations between metal ion complexation values and thermal properties

A series of heavy metal complexes of crosslinked chitosans were evaluated by thermogravimetric studies. The metal complexes with Cu, Cd and Hg ions exhibiting the highest complexing ability to chitosans (Hg 354–364, Cu 100–112, and Cd 121–160, in mg/g chitosan), had the lowest onset of degradation temperatures (range 194–210 °C) and the lowest final degradation temperatures (generally less than 294–304 °C for Hg, 296–338 °C for Cu, and 305–368 °C for Cd complexes). Mn ion, with the lowest binding to chitosans (Mn 5–7 mg/g), showed the reverse behavior, having onset (240–248 °C) and final degradation temperatures (range 300–368 °C). Zn (binding 74–87 mg/g) and Pb (binding 39–62 mg/g) ions have a binding ability intermediate to Cu/Cd/Hg and Mn extremes, and therefore the effects on onset and final degradation temperatures are intermediate to these values.     

The influence of pH and chloride on the retention of cadmium,lead, mercury,and zinc by soils

The extent of contamination of soils by toxic heavy metals not only depends on the rate of loading of the metal but also on the nature of the adsorbing surfaces, the degree of alkalinity or acidity of the soil and the presence of aqueous complexant ligands. This work reports on the role of pH on the retention of Cd, Hg, Pb and Zn by two soils and on the influence of the chloride, Cl‐, ion on the chemical speciation and retention of the four metals. Batch adsorption experiments were conducted from pH 3 to 7 in the presence of either 0.1 M LiCl or LiClO₄. The results of the study showed that high concentrations of Cl^‐ ions can greatly decrease the retention of Hg and have an increasingly lesser effect on Cd, Pb and Zn retention. The effect of the Cl^‐ons was directly related to the metal‐Cl formation constants. The results of computer modeling of Cd and Hg retention by goethite and humic acid fractions indicated the relative importance of aqueous vs. surface complexation on metal retention. For organic surfaces, which do not form ternary surface complexes, the presence of aqueous complexant ligands should always decrease the adsorption of the metal. For mineral surfaces, which do form ternary surface complexes, there may be increased or decreased metal retention depending on the formation constant of the aqueous metal‐ligand species, the intrinsic complexation constants for the various binary and ternary complexes of the metal and the concentration of the complexant ligand. Thus for Hg, which forms very strong aqueous species with Cl^‐ ions, reduced adsorption on goethite was predicted in the presence of 0.1 M LiCl, while enhanced adsorption was predicted for Cd and Pb. The results suggest caution in the disposal of Cl‐containing wastes onto metal‐contaminated soils. The deleterious effects of Cl^‐ ion addition would be greatest for soils with relatively high organic matter contents and low contents of hydrous ferric oxides.     

Synthesis, spectroscopy and electrochemistry of some polynuclear complexes of aminoethanethiol

Polynuclear S-bridged complexes of the general formula {[Co₂L₆]M}ⁿ⁺ with M = Co(III), Cd(II), Pb(II), Ni(II), Zn(II) and Hg(II) were prepared from [Co(2-aminoethanethiolate)₃] and the appropriate metal salt. Proton and ¹³C NMR spectra are consistent with structures previously proposed for these species with ¹³C chemical shifts dependent on the bridging metal ion. Electrochemical studies are consistent with a model in which an S-bonded ML₆ moiety (i.e., the bridging metal ion and the six aminoethanethiolate ligands) acts as a ‘dodecadentate’ ligand bonded to two Co³⁺ ions. Reduction of the terminal cobalt ions in these trinuclear complexes is observed in the range −0.75 to −1 V vs. SCE on mercury, gold or glassy carbon working electrodes. For complexes with relatively labile bridging ions, the electrode reaction is irreversible, presumably due to rapid decomposition of the labile cobalt(II) product. For the tricobalt(III) derivative, however, the electrode reaction is reversible consistent with other recent observations on cage or otherwise stereorestrictive ligand systems [1].     

包头南海子湿地三种鹭鸟羽毛与环境中重金属含量的关系

于2016年7至10月采用电感耦合等离子体发射光谱法(ICP-OES),测定了内蒙古包头南海子湿地繁殖期过后的白琵鹭(Platalea leucorodia)、苍鹭(Ardea cinerea)和夜鹭(Nycticorax nycticorax)3种鹭鸟初级飞羽及环境因子(水、土壤、食物)中As、Cd、Cr、Cu、Ni、Pb、Zn、Fe、Mn、Hg 10种重金属的含量,采用单因素方差分析方法比较了不同鹭鸟种类羽毛重金属含量差异,并通过生物富集系数及Pearson相关性检验分析了羽毛与环境因子间重金属含量之间的关系,以揭示包头南海子湿地环境中重金属污染现状及生物富集特征。结果表明:(1)被检测的10种重金属中,As、Cd、Cr、Cu、Pb、Zn、Hg 7种元素在湿地环境中均已超标,尤其土壤中Fe、Zn、Cu已达到重度污染的程度。(2)不同重金属元素在鹭鸟羽毛中的含量存在差异,其中Fe元素在白琵鹭羽毛中的含量水平最高(388.77 mg/kg),Cd元素在夜鹭羽毛中的含量最低(0.12 mg/kg)。在鹭鸟羽毛中重金属含量由高至低的顺序分别为,白琵鹭Fe、Zn、Mn、Cu、Hg、Cr、Ni、Pb、As、Cd,苍鹭Zn、Fe、Cu、Cr、Ni、As、Mn、Hg、Pb、Cd,夜鹭Zn、Fe、Mn、Cu、Ni、Pb、Hg、Cr、As、Cd。除Pb和Cd元素外,其他8种元素含量在3种鹭鸟羽毛中的含量种间差异显著。(3)相关分析表明,鹭鸟羽毛中的重金属含量与环境因子中的重金属含量显著相关且呈现富集特征,为此可作为监测当地环境污染的指示性材料。     

浙江油茶产地土壤和果实金属元素含量特征

为探讨油茶(Camellia oleifera)产地土壤和油茶果实中金属元素分布和富集特征,在油茶果实成熟期,对浙江5个油茶产地土壤及油茶果实中金属元素进行污染分析和富集能力评价.结果表明,浙江油茶产地土壤中Pb、Cr、Cd、As、Hg、Ni、Cu和Zn含量低于农用地土壤污染风险筛选值,综合污染等级为安全.个别产区常山...     

Differential effects of monovalent, divalent and trivalent metal ions on rat brain hexokinase

The effects of monovalent (Li+, Cs+) divalent (Cu2+, Ca2+, Sr2+, Ba2+, Zn2+, Cd2+, Hg2+, Pb2+, Mn2+, Fe2+, Co2+, Ni2+) and trivalent (Cr3+, Fe3+, Al3+) metals ions on hexokinase activity in rat brain cytosol were compared at 500 microM. The rank order of their potency as inhibitors of brain hexokinase was: Cr3+ (IC50 = 1.3 microM) greater than Hg2+ = Al3+ greater than Cu2+ greater than Pb2+ (IC50 = 80 microM) greater than Fe3+ (IC50 = 250 microM) greater than Cd2+ (IC50 = 540 microM) greater than Zn2+ (IC50 = 560 microM). However, at 500 microM Co2+ slightly stimulated brain hexokinase whereas the other metal ions were without effect. That inhibition of brain glucose metabolism may be an important mechanism in the neurotoxicity of metals is suggested.     

Effect of some metal ions on blood and liver delta-aminolevulinate dehydratase of Pimelodus maculatus (Pisces, Pimelodidae)

1. delta-ALA-D from Pimelodus maculatus was inhibited in vitro by Cd2+ greater than Pb2+ greater than Hg2+ greater than Cu2+ greater than Zn2+ in blood and by Pb2+ greater than Cd2+ greater than Hg2+ greater than Cu2+ = Zn2+ in the liver. 2. Kinetic analysis of the inhibition by the metal ions showed that Cd2+ and Hg2+ act as non-competitive inhibitors on both sources. 3. Pb2+ showed a mixed type of inhibition in blood and a non-competitive type in the liver. 4. Zn2+ acted as a competitive or mixed inhibitor, on both sources, depending on concentration.     

Metal ion-induced conformational changes in Escherichia coli alkaline phosphatase.

Ultraviolet difference spectra are produced by the binding of divalent metal ions to metal-free alkaline phosphatase (EC 3.1.3.1). The interaction of the apoprotein with Zn2+, Mn2+, Co2+ and Cd2+, which induce the tight binding of one phosphate ion per dimer, give distinctly different ultraviolet spectra changes from Ni2+ and Hg2+ which do not induce phosphate binding. Spectrophotometric titrations at alkaline pH of various metallo-enzymes reveal a smaller number of ionizable tyrosines and a greater stability towards alkaline denaturation in the Zn2+- and Mn2+-enzymes than in the Ni2+-, Hg2+- and apoenzymes. The Zn2+- and Mn2+-enzymes have CD spectra in the region of the aromatic transitions that are different from the CD spectra of the Ni2+-, Hg2+- and apoenzymes. Modifications of arginines with 2,3-butanedione show that a smaller number of arginine residues are modified in the Zn2+-enzyme than in the Hg2+-enzyme. The presented data indicate that alkaline phosphatase from Escherichia coli must have a well-defined conformation in order to bind phosphate. Some metal ions (i.e. Zn2+, Co2+, Mn2+ and Cd2+), when interacting with the apoenzyme, alter the conformation of the protein molecule in such a way that it is able to interact with substrate molecules, while other metal ions (i.e. Ni2+ and Hg2+) are incapable of inducing the appropriate conformational change of the apoenzyme. These findings suggest an important structural function of the first two tightly bound metal ions in enzyme.     

Metal accumulation by Halodule wrightii populations

Metal concentrations and population parameters of the seagrass Halodule wrightii were determined at three locations at Rio de Janeiro State, Brazil. The possible increase of metal availability in one of these areas, Sepetiba Bay, as a result of dredging of contaminated bottom sediments which ocurred, was evaluated by analyses of Al, Cd, Cr, Cu, Fe, Ni, Pb and Zn in root, rhizome and shoots. In addition, analyses were carried out in H. wrightii populations from non-contaminated areas located at northwestern (Cabo Frio) and southeastern (Angra do Reis) regions of Rio de Janeiro State. Concurrently, abundance and density data of the seagrass populations were obtained. It was found that concentration from Sepetiba Bay samples up to 1.6 ± 0.4 μg g⁻¹ of Cd, 12 ± 1.0 μg g⁻¹ of Cr, 27 ± 2.4 μg g⁻¹ of Pb, 291 ± 47 μg g⁻¹ of Mn, 128 ± 23 μg g⁻¹ of Zn were significantly higher than that from two other collection sites. An increase in Cd and Zn concentration was observed in H. wrightii from Sepetiba Bay indicating that metal mobilization from contaminated sediments through dredging activities were, at least in part, transferred to the biotic compartment via accumulation by the seagrass. The populations of seagrass within the region demonstrated quite substantial changes in biomass data but not in shoot or rhizome density during the study. Such changes in biomass are to be expected, as these dynamics are typical of the small, isolated monospecific populations of H. wrightii along the Rio de Janeiro coast.     

湘西河流表层沉积物重金属污染特征及其潜在生态毒性风险

花垣河和峒河是湘西地区受到锰矿和铅锌矿生产影响严重的两条河流。通过表层沉积物采样分析了Cd、Pb、Cu、Ni、Cr、Zn和Mn的总量,根据BCR连续提取程序分析沉积物样品中重金属的地球化学赋存形态,采用内梅罗指数法和地积累指数法评价了沉积物重金属污染特征,根据重金属的富集程度探讨了重金属污染来源,采用淡水生态系统沉积物质量基准(SQGs,TEL/PEL)和毒性单位评价了花垣河和峒河沉积物中重金属元素的生态毒性风险。结果表明,花垣河和峒河绝大多数位点的表层沉积物中Cd、Pb、Cu、Ni、Cr、Zn和Mn的总量高于参照点,形成严重的复合污染,花垣河沉积物中重金属的污染水平明显高于峒河,但沿程变化规律不明显,而峒河沉积物中重金属的沿程变化较有规律,即上游含量低,中下游含量较高。两条河流表层沉积物中富集程度居前列的均为Cd、Pb、Zn和Mn。花垣河和峒河沉积物重金属污染主要来源于矿业生产所产生废渣和废水的点排放。在花垣河和峒河的大多数位点,Cd、Pb和Mn的形态具有共同特征,其生物可利用态均较大程度地超过生物不可利用态,而且Mn和Cd的生物可直接利用态所占比例远高于其它重金属,而Cu和Cr的生物可直接利用态所占比例很低。花垣河沉积物中Cd、Pb和Zn在所有位点极大地超过PEL,在峒河中下游,Cd、Pb、Ni和Zn超过PEL,具有较大的潜在生物毒性。除上游S1位点外,花垣河的其余各位点都具有明显的急性毒性,峒河中下游各位点具有明显的急性毒性,这些河段需要重点治理。     

Cytogenetical Toxical Effects of Heavy Metals on Vicia faba and Inquires into the Vicia Micro nucleus

Under the treatment of heavy metal ions Pb2+, Cd2+ and Hg2+, the interval of mitotic stage was shortened, and the time of interphase prolonged so that the cell cycle was prolonged in the root-tip cells of broadbean (Vicia faba L. ). With the increase of concentrations of Pb2+, Cd2+ and Zn2+ below 1.0, 0.01 and 10 ppm respectively, the mitosis index (IM) rose in root-tip cells, but IM decreased when the root-tips were treated with the some heavy metal ions above the above-mentioned respective concentrations. IM was inhibited in Hg2+ of any concentrations. Within the concentration of Pb2+, Cd2+, Hg2+ and Zn2+ below 1.0, 0. 50, 5.0, 100.0 ppm respectively, the frequency of micronucleus (MCNF) rose as the concentrations were increased, and lowered as the respective concentrations exceeded those stated above. Similar changes occurred in the frequency of chromosomal aberrations (CAF) when the concentration of Pb2+, Cd2+, Hg2+, Zn2+ were below or above 5.0, 5.0, 0.50, 100.0 ppm respectively. Mn2+ had no significant effects to them. By data processing with the method of gray system control and computer aided drawing to IM, MCNF and CAF, it was shown that the three parameters varied tremendously in different dose-effect ranges. All of which suggested that in order to obtain a reliable results in the environmental monitoring and hazardous material detection, genetoxicity inspection should be carried out under the optimal condition when (1) the concentration of the heavy metal to be detected does not seriously inhibit mitosis and (2) CAF and MCNF is in positive correlation.     

Pollution Assessment and Potential Sources of Heavy Metals in Agricultural Soils around Four Pb/Zn Mines of Shaoguan City,China

A total of 455 agricultural soil samples from four nonferrous mines/smelting sites in Shaoguan City, China, were investigated for concentrations of 10 heavy metals (As, Cd, Co, Cr, Cu, Hg, Mn, Ni, Pb, and Zn). The mean concentrations of the metals were 72.4, 5.16, 13.3, 54.8, 84.5, 1.52, 425, 28.2, 529, and 722 mg kg^?1, respectively. The values for As, Cd, Hg, Pb, and Zn were more than 8 and 1.5 times higher than their background values in this region and the limit values of Grade II soil quality standard in China, respectively. Estimated ecological risks based on contamination factors and potential ecological risk factors were also high or very high for As, Cd, Hg, and Pb. Multivariate analysis (Pearson's correlation analysis, hierarchical cluster analysis, and principal component analysis) strongly implied three distinct groups; i.e., As/Cu/Hg/Zn, Co/Cr/Mn/Ni, and Cd/Pb. Local anomalies for As, Cu, Hg, and Zn by a probably anthropogenic source (identified as mining activity), Co, Cr, Mn, and Ni by natural contribution, and a mixed source for Cd and Pb, were identified. This is one of the few studies with a focus on potential sources of heavy metals in agricultural topsoil around mining/smelting sites, providing evidence for establishing priorities in the reduction of ecological risks posed by heavy metals in Southern China and elsewhere.     

The properties of the Mn, Ni and Pb transport operating at plasma membranes of cucumber roots

To avoid metal toxicity, plants have developed mechanisms including efflux of metal ions from cells and their sequestration into cellular compartments. In this report, we present evidence for the role of plasma membrane efflux systems in metal tolerance of cucumber roots. We have identified the plasma membrane-transport system participating in Cd, Pb, Mn and Ni efflux from the cytosol. Kinetic characterization of this proton-coupled transport system revealed that it is saturable and has a different affinity for each of the metal ions used (with Km 5, 7.5 and 0.1 m M for Mn, Ni and Pb, respectively). Treatment of cucumber roots with 100 μ M Cd prior to the transport measurements caused a great increase (over 250%) in Cd antiport activity in plasmalemma vesicles. After decreasing the metal concentration to 50 μ M we still observed a large increase (over 150%) of this activity in comparison with the control. Moreover, the addition of 50 μ M Cd to the external solution stimulated not only Cd antiport in the plasmalemma vesicles but also the antiport of other metals used in the experiments. Treatment of cucumber roots with 50 μ M Ni revealed a similar effect: the antiport activity of Cd, Mn, Ni and Pb was stimulated, although to a lesser extent in comparison with stimulation by Cd. The data indicate that the root plasma membrane antiporter system is stimulated by the exogenous presence of heavy metals.     

四种金花茶组植物叶片金属元素含量及富集特性研究

以四种金花茶组植物为研究对象,采用原子吸收光谱法和原子荧光法,测定其嫩叶、老叶及对应土壤中Mg、Ca、Mn、Fe、Zn、Ni、Se、Pb、Cd、Hg、As共11种元素的含量,并分别计算嫩叶和老叶对土壤金属元素的富集系数.结果表明:(1)4种金花茶组植物叶片富含Mg、Ga、Mn、Fe、Zn、Ni等营养元素,各元素在叶片中含量为Ca>Mg>Mn>Fe>Zn>Ni>Se;Pb、Cd、As、Hg等重金属元素含量较低,均达到无公害茶叶标准.(2)老叶和嫩叶中各金属元素含量差异较大,老叶中的Ca、Mn、Fe、Zn、Pb、Cd、Hg、As、Se元素含量均大于嫩叶,尤以Ca、Mn、Fe差异显著;嫩叶中的Mg和Ni含量大于老叶.(3)金花茶组植物对不同金属元素的富集能力不同,对各元素富集能力强弱为Ca、Mn、Mg>Zn、Ni、Hg>Pb、Se>Fe、As,老叶和嫩叶的富集规律存在差异.(4)不同金花茶组植物对金属元素的富集能力有较大差异,龙州金花茶(Camellia longzhouensis)和黄花抱茎茶(C.murauchii)对Mg、Ca、Mn、Zn、Ni、Se、Pb的富集能力均大于金花茶(C.nitidissima)和毛籽金花茶(C.ptilosperma).其中,龙州金花茶对Mg、Mn、Se的富集能力最强,黄花抱茎茶对Ca、Pb、Hg富集能力最强,金花茶对Hg的富集能力较强,对其它元素的富集能力均较弱;毛籽金花茶对Ca、Mn、Ni、Zn的富集能力均最弱.该研究结果为金花茶组植物的进一步开发和利用提供了理论依据.     

The binding of metal ions to ATP: A proton and phosphorus nmr investigation of diamagnetic metal-ATP complexes

Phosphorus and proton nmr spectra were recorded for complexes of ATP with Mg(II), Ca(II), Sr(II), Zn(II), Cd(II), Sn(II), Pb(II), Hg(II), Ag(I), and Tl(I) ions. Each of these ions except Hg(II) affected the ³¹P nmr of ATP, usually by shifting all three resonances downfield and decreasing the ³¹P-³¹P coupling constants. Pb(II) exerted the greatest shifts, while Mg(II) caused the greatest change in coupling constants. Effects on the adenine proton resonances were generally small and attributable to base stacking, but a direct metal-adenine binding is likely for Zn(II), Cd(II), and Ag(I). Effects on the ribose proton resonance were small in all of the ATP complexes, but were much larger in Zn(II)ADP and Cd(II)ADP. Formation of metal-bis(nucleotide) complexes occurred with Sn(II), Zn(II), and Cd(II).     

广西马尾松人工林对重金属元素的吸收、累积及动态

探讨了广西马尾松人工林对重金属Cu、Zn、Mn、Pb、Ni、cd元素的吸收、累积及动态。结果表明:马尾松林地土壤层(0~60 cm)中重金属元素Cu、Zn、Mn、Pd、Ni、Cd的平均含量,分别为23.02,24.46,235.46,5.93.8.45和0.14 mg·kg-1,储量大小依次为Mn>Zn>Cu>Ni>Pb>Cd。马尾松林不同组分中,重金属元素的含量范围分别为Cu 2.97-13.47,Zn 12.09-42.93,Mn 143.14-751.78,Pd 2.87-25.12,Ni 0.19-25.05和Cd 0.16~1.24 mg·kg-1,对土壤6种重金属元素富集能力的大小依次为Cd>Mn>Pb>Zn>Ni>Cu。马尾松林中,重金属元素的总储量为39.791kg·hm-2,其中Mn、Zn、Pb、Cu、Cd、Ni元素的储量分别为34.047,3.351,1.226,0.874,0.245,0.084 kg·hm-2,各组分中重金属元素储量的空间分布为干>皮>根>叶>枝。Cu、Zn、Mn、Pd、Ni、Cd的周转期分别为13.9、7.0、3.1、20.4、2.1、12 a,流动系数为Ni>Mn>Zn>Cd>Cu>Pb。     

Interaction of metal ions with lupin seed conglutin gamma

Various metal ions were capable of aggregating and precipitating conglutin gamma, an oligomeric glycoprotein purified from Lupinus albus seeds, at neutral pH values. The most effective metal ions, at 60-fold molar excess to the protein, were Zn2+, Hg2+ and Cu2+; a lower influence on the physical status of conglutin gamma was observed with Cr3+, Fe3+, Co2+, Ni2+, Cd2+, Sn2+, and Pb2+, while Mg2+, Ca2+ and Mn2+ had no effect at all. The insolubilisation of the protein with Zn2+, which is fully reversible, strictly depended on both metal concentration and pH. with middle points of the sharp transitions at three-fold molar excess and pH 6.5, respectively. Conglutin gamma is also fully retained on a metal affinity chromatography column at which Zn2+ and Ni2+ were complexed. A drop of pH below 6.0 and the use of chelating agents, such as EDTA and imidazole, fully desorbed the protein. A slightly lower binding to immobilised Cu2+ and Co2+ and no binding with Mg2+, Cd2+ and Mn2+ were observed. The role of the numerous histidine residues of conglutin gamma in the binding of Zn2+ is discussed.     

Vertical and Horizontal Distributions of Zn,Cd, Pb,Cu, and Hg in Uncultivated Soil in the Vicinity of a Zinc Smelter at Odda,Norway

In the present work the extent and variation of Zn, Cd, Pb, Cu, and Hg loading in undisturbed surface soil (0–5 cm) and the vertical transport of the metals in soil profiles are studied in the vicinity of a zinc smelter in Norway. Three major controlling factors on the metal concentrations in soil have been assessed: 1) distance from the anthropogenic point source; 2) organic matter content (O.M.); and 3) the prevailing wind directions. Moreover metal distributions in proximal soil profiles in 1972 and 2003 are compared. Current concentrations of Zn, Cd, Pb, Cu, and Hg in surface soil reach 14000, 60, 980, 430, and 7.0 mg·kg ^{? 1} , respectively, near the smelter and decrease regularly with distance in the northerly direction according to the regression model (y = ax^{? b} ). The Zn concentrations are significantly different from the background range up to 30 km from the smelter, whereas the other metals approach background at only 10 km distance. Subsurface concentration peaks of Pb, Cu, and Hg are found at greater depth in soil profiles than peaks of Zn and Cd. Levels of Zn, Cd, and Pb in surface soil seem to have decreased from 1972 to 2003, whereas for Cu the levels appear not to be significantly different.     

Synthesis of diethylaminoethyl dextran hydrogel and its heavy metal ion adsorption characteristics

Epichlorohydrin-crosslinked diethylaminoethyl dextran (DEAE-D/ECH) hydrogel was synthesized by intermolecular side-chain reaction of DEAE-D hydroxyl groups with monomeric crosslinking agent, ECH. Swelling ability, adsorption capacity and metal removal of the hydrogel were profoundly determined and some structural parameters for the hydrogel such as volume of non-swollen gel, percentages of gellation, swelling ratio and equilibrium water content were evaluated in this study. The ability of removing heavy metal ions from Orontes River by the synthesized hydrogel, thoroughly characterized by photometric spectrometer and the adsorption characteristics of metal ions, was investigated as well as surface morphologies of the hydrogel before and after metal adsorption were examined by SEM. Structure of DEAE-D/ECH gel was analyzed by FTIR, TGA, and DSC. Gellation point of binary system reaction between DEAE-D and ECH was determined via monitoring viscosity changes during reaction. The order of affinity based on amount of metal ion uptake was found as follows: Zn(2+)>Mn(2+)>Pb(2+)>Cd(2+).