Speciation of trace metals in sediments of a tropical estuary     

C. K. Nair  A. N. Balchand 《Environmental Geology》1993,21(1-2):96-102

Axial surveys were performed in the two river tributaries of the Cochin estuary, SW India during November 1988. Surficial sediments were subjected to sequential chemical extractions to delineate five metal fractions, namely, exchangeable, carbonate bound, easily reducible, organic/sulfide bound, and residual. The results indicated selective accumulation of Mn and Ni in carbonate bound and organic/sulfide forms, along with marginal amounts of Co in the exchangeable fraction. Large portions of Fe and Cr occurred in the residual fraction, whereas composite fractionation of Zn species was noticed. The exchangeable fractions of Fe and Cr as well as of easily reducible cobalt were below detection limits. The levels of Cr and Zn indicate anthropogenic inputs in this estuary, whereas Co and Ni show regional contamination exceeding natural levels. The analytical speciation procedure helps to deduce the sedimental diagenetic processes in the estuarine environment.  相似文献   

APPLICATION OF PATTERN RECOGNITION TO SPECIATION DATA OF HEAVY METALS IN SUSPENDED PARTICULATES OF URBAN AIR     

X.TOMAS  J.RIUS  J.OBIOLS  A.SOL 《地理学报(英文版)》1988,(Z1)

In order to get a better knowledge of the air pollution levels of the urban air of Barcelona,twelvesamples from three stations of the air-monitoring control network were analysed.Each control station isrepresentative of a different environmental situation.Thus the station at Plaa Molina responds to asimple domestic and urban traffic situation;the station at Poble Nou to the influence of medium andsmall industries,mainly metallurgical;and the station at Montcada to a zone in which there existimportant industries,a cement factory,two highways and railroads.The total content of unsedimentable particles,three inorganic anions(chlorides,sulphates andnitrates)and six heavy metals(Fe,Pb,Cu,Mn,Cr and Cd)were determined on all the samples obtainedduring the same period of time.The use of an analytical scheme of sequential extraction has alsopermitted the subdivision of the total content of each metal into the following four fractions:(1)solubleor exchangeable;(2)associated with carbonates and/or with iron and manganese oxides;(3)bound toorganic matter;and(4)residual.The use of principal component analysis applied to the data as a whole showed the associations andcorrelations between the various parameters as well as between the different above mentioned fractions.The predominant presence of Cd in the‘soluble or exchangeable’fraction is confirmed,while the othermetals are mainly associated with the‘carbonates and/or Fe and Mn oxides’and‘bound to organicmatter’fractions.Hierarchical cluster analysis applied to the twelve samples showed clearly the presence of threedifferent classes closely related to the origin(station)of the samples.Thus it becomes feasible to proposefor each station a possible profile of the content in terms of the different parameters considered.  相似文献   

The speciation of dissolved copper,cadmium and zinc in Manila Bay,Philippines     

Velasquez IB  Jacinto GS  Valera FS 《Marine pollution bulletin》2002,45(1-12):210-217

At present, there is a very limited information on the levels and distribution of dissolved metals in Manila Bay. In this study, the horizontal and vertical distribution of operationally defined species (labile, bound and total) of dissolved copper (Cu), cadmium (Cd) and zinc (Zn) were determined using differential pulse anodic and cathodic stripping voltammetry in water samples obtained from 18 stations in November 1998. In addition, the 24-h variability in the concentrations of these species at different depths in the water column was determined. These measurements were complemented by the determination of temperature, salinity, dissolved oxygen, chlorophyll a, particulate organic carbon and nutrients. Results showed that more than 50% of total dissolved copper and cadmium were labile while 50% of total dissolved zinc was organically bound. Vertical profiles showed that Cu, Cd and Zn concentrations were generally high at the surface. Zinc and cadmium were characterised by the presence of a mid-depth minimum while copper did not show any clear vertical trend.

Dissolved Cu concentrations during the spatial and diurnal samplings ranged from 0.32 to 6.95 nM and 1.52 to 45.65 nM, respectively. For Cd, the concentrations in 18 stations ranged from 0.05 to 2.92 nM, and from 0.03 to 2.42 nM over a 24-h period. Zn concentrations ranged from 2.48 to 147.43 nM and 2.87 to 88.27 nM during the spatial and diurnal samplings, respectively. The large variation in the concentration of Cu, Cd and Zn in the bay was observed to be associated with the presence of a large vertical density gradient in the water column, which appeared to limit the exchange of materials between the surface and bottom waters. Elevated levels of these metals near point sources suggest anthropogenic inputs in the bay.  相似文献   

Contamination risk assessment of fresh groundwater using the distribution and chemical speciation of some potentially toxic elements in Calabar (southern Nigeria)     

A.?E.?EdetEmail author  B.?J.?Merkel  O.?E.?Offiong 《Environmental Geology》2004,45(7):1025-1035

The computer program PHREEQC was used to determined the distribution, chemical speciation and mineral saturation indices in a fresh groundwater environment with limited mining activities in the adjoining areas. The aim was mainly to determine the potential risk of a coastal plain aquifer contamination by some potentially toxic elements. The results show that the elements Ba, Cd, Cu, Fe, Mn, Ni, Rb, Sr, and Zn are distributed as free metal ions. Arsenic is in the neutral form of H₃AsO₃ ^o, while three species of aluminium [Al³⁺, AlOH₂, Al(OH)₂ ⁺] dominate. The major species of uranium include UO₂CO₃, UO₂²⁺+, UO₂⁺, and UO₂OH⁺, respectively, in order of abundance. The groundwater is saturated with respect to alunite [KAl₃ (SO₄)₂ (OH)₆], basaluminite [Al₄ (OH)₁₀ SO₄], boehmite [Al(OH)], Cu metal (Cu), cuprous ferrite (CuFeO₂), diaspore [AlO(OH)], gibbsite [Al(OH)₃], goethite (FeOOH), hematite (Fe₂O₃), magnetite (Fe₃O₄) and uraninite (UO₂). Most of the species are not mobile under the prevailing pH (3.3 to 5.9) and Eh (7 to 158 mV) conditions. The mobile ones are very low in concentration and will be immobilized by precipitation of mineral phases. The study concludes that presently these species do not pose any risk to the aquifer.  相似文献   

Arsenic in mine waters: an international study   总被引：4，自引：4，他引：4  

M. Williams 《Environmental Geology》2001,40(3):267-278

 Hydrochemical data are presented for arsenic (As) in the mine waters of 34 gold and base-metal mining localities in seven countries of south-east Asia, Africa and Latin America, encompassing contrasting climatic settings and at least eight discrete styles of primary mineralization. Peak dissolved As concentrations at these sites range from 0.005–72 mg/l, with the United States Environmental Protection Agency (US-EPA) potable water threshold of 50 μg/l exceeded in 25 cases. Arsenate (As⁵⁺) constitutes the dominant species at over 80% of sites. Very high dissolved As concentrations (>1 mg/l) show no systematic between-site relationship with mine water pH/Eh regime. Important determinants of mine water As fluxes include iron hydrochemistry, the presence of cyanic ore processing effluents, site geology, the paragenetic sequence that follows sulphide oxidation, climate and mine management. Human toxicological impacts of As contamination have been recognized at only one case-study site, with a further four considered to warrant more detailed risk assessment. Received: 2 November 1999 · Accepted: 21 March 2000  相似文献   

Two Experimental Methods to Determine the Speciation of Cadmium in Sediment from the River Neckar     

N. Martin  I. Schuster  St. Peiffer 《洁净——土壤、空气、水》1996,24(2):68-76

The binding forms of Cd to an anaerobic sediment of low sulfide content from Lauffen reservoir (River Neckar, Germany) were studied using two different approaches, i. e. sequential extraction (modified from published protocols) and titrimetric study of the pH-dependent Cd release. Thermodynamic equilibrium calculations were applied to calculate both the release pattern of Cd during the titrations and the speciation of Cd within the single fractions of the extraction protocol. The calculations were based on measured sediment parameters such as hydrous ferric oxide (HFO), acid volatile sulfide, carbonate content and total Cd content, and the extractants (oxalate, acid etc.) used. The results of the two independent approaches coincided well in that they both assigned more than two thirds of the total Cd content to be adsorbed to organic matter. Cd bound as CdS is of little importance. Sequential extraction after a 3-month oxidation period at pH 7 revealed a shift of Cd from being mainly bound in stronger surface complexes with organic matter to being mainly bound in weaker surface complexes with organic matter and HFO, and thus becoming more bioavailable. This study suggests that the use of sequential extraction although being frequently criticized due to its operational character can be used to determine binding forms of metal ions if they are accompanied by 1) careful supporting experiments, 2) analysis of important sediment parameters, and 3) the use of thermodynamic equlibrium models which can help to understand Cd speciation within the extraction fractions.  相似文献   

Mercury mobility in mine waste from Hg-mining areas in Almería,Andalusia (Se Spain)     

Andrés Navarro  Esteve Cardellach  Mercé Corbella 《Journal of Geochemical Exploration》2009

Mining wastes and calcines from two abandoned mining areas (Valle del Azogue and Bayarque in Almería) have been characterized. In the mining wastes, the dominant mercury phases are cinnabar and elemental mercury in the matrix. In the calcines, however, the dominant mercury phase is elemental mercury bounded to the matrix. Water-leaching experiments were conducted on low-grade stockpiles and calcines in order to simulate the mobilization of mercury by runoff under environmental conditions. The laboratory column-leaching experiments show a possible mobilization of mercury from Hg⁰ dissolution, colloid transport and a possible dissolution of calomel and other soluble phases in the mine wastes from the Valle del Azogue and Bayarque mines. Equilibrium speciation modeling of Hg, conducted using the numerical code MINTEQ, showed that the theoretical dominant mercury species in the calcine and mining wastes samples are Hg(OH)₂, HgCl₂, HgClOH and Hg⁰. In some leachates obtained from the Valle del Azogue mining wastes (sample A06), the high Hg concentrations may indicate the possible dissolution of mineral phases such as calomel and other soluble phases, which are subsaturated. The environmental results indicate a great environmental mobility of mercury, especially during wet episodes associated with intense precipitation events, when there are significative amounts of secondary soluble minerals.  相似文献   

Speciation and Determination of Inorganic Mercury and Methylmercury by Headspace Single Drop Microextraction and Electrothermal Atomic Absorption Spectrometry in Water and Fish     

Deniz Yurtsever Sarıca  Ali Rehber Türker 《洁净——土壤、空气、水》2012,40(5):523-530

In this study, headspace single drop microextraction (HS‐SDME) method in combination with electrothermal atomic absorption spectrometry (ETAAS) method was developed and validated for the speciation and determination of inorganic mercury (iHg) and methylmercury (MeHg). MeHg and iHg species were reduced to volatile methylmercury hydride (CH₃HgH) and elemental mercury, respectively, in the presence of NaBH₄ and trapped onto a drop of acceptor phase in the tip of a microsyringe. Thiourea and ammonium pyrrolydinedithiocarbamate (APDC) were tested as the acceptor phase. The experimental parameters of the method such as microextraction time, temperature, NaBH₄ concentration, acceptor phase concentration, and pH of the medium were investigated to obtain distinctive conditions for mercury species. Possible interference effects have also been investigated. In order to validation of the method, analytical figures of merits such as accuracy, precision, limit of detection (LOD), limit of quantitation (LOQ), and linear working range have been evaluated. Accuracy of the method has been verified by analyzing certified reference materials (BCR 453 Tuna fish) and spiked samples. The proposed method was applied for the speciation and determination of mercury species in water and fish samples. Mercury species (MeHg and iHg) have been determined in the real samples with a relative error less than 10%.  相似文献   

Distribution and speciation of mercury in surficial sediments from main mangrove wetlands in China   总被引：4，自引：0，他引：4  

Z.H. Ding  J.L. Liu  L.Q. Li  H.N. Lin  H. Wu  Z.Z. Hu 《Marine pollution bulletin》2009,58(9):1319-1325

The purpose of this study was to establish the distribution, speciation and bioavailability of mercury in mangrove sediments. A systemic survey of surficial sediments from 13 mangrove wetlands of China was carried out. Hg concentrations ranged from 2.3–903.6 ng g⁻¹, with an average value of 189.4 ng g⁻¹. Of the 13 areas surveyed, the Hg content in sediments was similar to background levels in 6 areas but was much higher in the other seven areas. Hg levels were affected by natural and anthropogenic factors, including terrestrial pollutants, geomorphic properties, and indirectly by economic status. Hg levels were positively correlated with organic matter, pH, and silt and clay fractions, but Hg was negatively correlated with sand fraction. In most mangrove wetlands, Hg existed primarily in the form of volatile Hg. Hg is easily bioaccumulated in mangrove wetlands and may be the natural source of Hg emissions to the atmosphere.  相似文献   

Reductive dissolution of arsenical ferrihydrite by bacteria     

《Applied Geochemistry》2016

Mining and metallurgical processing of gold and base metal ores can lead to the release of arsenic into the aqueous environment as a result of the weathering and leaching of As-bearing minerals during processing and following disposal. Arsenic in process solutions and mine drainage can be effectively stabilized through the precipitation of ferrihydrite. However, under anaerobic conditions imposed by burial and waste cover systems, ferrihydrite is susceptible to microbial reduction. This research, stimulated by the paucity of information and limited understanding of the microbial reduction of arsenical ferrihydrite, was conducted on synthetic adsorbed and co-precipitated arsenical 6-line ferrihydrite (Fe/As molar ratio of 10/1) using Shewanella sp. ANA-3 and Shewanella putrefaciens CN32 in a chemically defined medium containing 0.045 mM phosphate concentration. Both bacteria were equally effective in their reducing abilities around pH 7, resulting in initial rates of formation of dissolved As(III) of 0.10 μM/h for the adsorbed, and 0.08 μM/h for the co-precipitated arsenical 6-line ferrihydrite samples. The solid phases in the post-reduction samples were characterized by powder X-ray diffraction (XRD), micro-XRD, scanning electron microscopy (SEM), transmission electron microscopy (TEM), electron microprobe and X-ray absorption spectroscopy (XAS) techniques. The results indicate the formation of secondary phases such as a biogenic Fe(II)–As(III) compound, akaganeite, goethite, hematite and possibly magnetite during bacterial reduction experiments. Holes and bacterial imprints measuring about 1–2 μm were observed on the surfaces of the secondary phases formed after 1200 h of reduction. This study demonstrates the influence of Fe and As reducing bacteria on the release of significant concentrations of more mobile and toxic As(III) species from arsenical 6-line ferrihydrite, more readily from the adsorbed than from the co-precipitated ferrihydrite.  相似文献