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Speciation and leachability of copper in mine tailings from porphyry copper mining: influence of particle size.

Mine tailing from the El Teniente-Codelco copper mine situated in VI Region of Chile was analysed in order to evaluate the mobility and speciation of copper in the solid material. Mine tailing was sampled after the rougher flotation circuits, and the copper content was measured to 1150 mg kg (-1) dry matter. This tailing was segmented into fractions of different size intervals: 0-38, 38-45, 45-53, 53-75, 75-106, 106-150, 150-212, and >212 microm, respectively. Copper content determination, sequential chemical extraction, and desorption experiments were carried out for each size interval in order to evaluate the speciation of copper. It was found that the particles of smallest size contained 50-60% weak acid leachable copper, whereas only 32% of the copper found in largest particles could be leached in weak acid. Copper oxides and carbonates were the dominating species in the smaller particles, and the larger particles contained considerable amounts of sulphides.

Adsorption↗

Speciation of Cd and Zn in contaminated soils assessed by DGT-DIFS, and WHAM/Model VI in relation to uptake by spinach and ryegrass.

A pot experiment was carried out to investigate the impact of Cd and Zn extractability in soil and speciation in pore water of industrial contaminated soils, on metal concentration in a metal sensitive species like spinach (Spinacia oleracea) and a more metal tolerant species like Italian ryegrass (Lolium multiflorum). For chemical speciation of Cd and Zn in pore water, WHAM/Model VI version 6.0 was used. The DGT technique was used to determine the effective concentration, C(E), of Cd and Zn in soils. The free ion activity in pore water correlated well with the contents in plants, and there was a linear relationship between the C(E) values and the concentration of Cd and Zn in both spinach and ryegrass in the non-toxic range. However, the C(E) values usually overestimated the plant contents when plants, particularly the spinach plants, were subjected to toxic concentration in the pore water. Metal uptake decreased in plants affected by toxicity, whereas metal binding to the Chelex resin did not. Thus, we found no linear relationship between the C(E) and metal contents in spinach, whereas a linear relationship was found between C(E)-Zn and the Zn concentration in ryegrass (r2=0.96, p<0.001). For Cd in ryegrass this relationship was weak (r2=0.53, p=0.18). This study indicates that the transport of metals from labile metal pools to the DGT-resin is linearly related to plant uptake only when plants are growing well, and that the applicability of DGT as an indicator for plant uptake seems species dependent.

Biodegradation, Environmental↗

Speciation of heavy metals during co-composting of sewage sludge with lime.

During composting the humification of organic matter will have a significant effect on the physicochemical form of existence of heavy metals. Therefore the present study was conducted to investigate the effect of co-composting sewage sludge with lime on heavy metal speciation and the changes in DTPA extractable metals. Metal speciation was conducted to evaluate the redistribution of Cu, Mn, Ni, Pb and Zn in sewage sludge composted with lime. Sewage sludge was mixed with sawdust in 2:1 (w/w fresh weight) and then composted with lime at 0%, 0.63%, 1% or 1.63% (dry weight) for 100 days. The lime addition did not cause any changes in the different forms of Cu and Mn, but the composting process caused transformations of residual form of Cu and Mn into oxidizable and reducible form, respectively. For Ni, the reducible form was mainly transformed into residual form and lime addition decreased this transformation. Major transformation of different forms of Pb was not found, however the residual form of Pb increased with lime addition. The predominant residual form of Zn was mainly transformed into oxidizable form and the lime addition reduced this transformation. Addition of lime to sewage sludge during composting resulted in lower DTPA extractable metal contents. Therefore, lime is a suitable material to co-compost with sewage sludge to reduce the availability of heavy metals.

Calcium Compounds↗

The distribution, solid-phase speciation, and desorption/dissolution of As in waste iron-based drinking water treatment residuals.

Arsenic concentrations and solid-phase speciation were assessed as a function of depth through Fe-media beds for two commercially available products (Granular Ferric Hydroxide-GFH and Bayoxide E33-E33) from pilot-scale water treatment field tests. These results were compared with data from solution (de-ionized water-DI-H2O) concentrations of As equilibrated with Fe-media in an anoxic environment at 4 degrees C. The materials had a high capacity for As (GFH media 9620 mg kg(-1) As, E33 Media 5246 mg kg(-1)). Arsenic concentrations decreased with bed depth. For E33, X-ray absorption near-edge spectroscopy results showed that As(V) was the dominant solid-phase species. For GFH, As(III) was detected and the proportion (relative to As(V)) of As(III) increased with bed depth. Arsenic concentrations in DI-H2O equilibrated with the media were low (35 microg l(-1)) over a period of 50 d. Arsenic concentrations in the equilibrated solutions also decreased with depth. Results from tests on soluble As speciation show that As in solution is in the form of As(V). Kinetic desorption experiments carried out at different pH values (3, 5, 7, 8, and 9) show that the media exhibit some acid/base neutralization capacity and tend to bind As sufficiently. Concentrations of As in the pH desorption experiments were in the same order of magnitude as the toxicity characteristic leaching procedure extractions (tens of microgl(-1)) except at low pH values. For the GFH media tested at a pH of three, As increases in solution and is mainly associated with colloidal (operationally defined as between 0.1 and 1.0 microm) iron.

Arsenic↗

Speciation of V, Cr and Fe by capillary electrophoresis-bandpass reaction cell inductively coupled plasma mass spectrometry.

Capillary electrophoresis-dynamic reaction cell inductively coupled plasma mass spectrometry (CE-DRC-ICP-MS) for the speciation of iron(III/II), vanadium(V/IV) and chromium(VI/III) is described. Two different CE migration modes were employed for separating the six metal ions using pre-capillary complexation. One is counter-electroosmotic mode in which iron(III/II) and vanadium(V/IV) ions were well separated using a 60 cm x 75 microm i.d. fused silica capillary. The voltage was set at +22 kV and a 15 mmol l(-1) tris(hydroxymethyl)aminomethane (Tris) buffer (pH 8.75) containing 0.5 mmol l(-1) ethylenediaminetetraacetic acid (EDTA) and 0.5 mmol l(-1) ortho-phenanthroline (phen) was used as the electrophoretic buffer. The other is co-electroosmotic mode in which chromium(VI/III) ions were well separated while the applied voltage was set at -22 kV and a 10 mmol l(-1) ammonium citrate buffer (pH 7.7) containing 0.5 mmol l(-1) diethylenetriaminepentaacetic acid (DTPA) and 0.01% polybrene was used as the electrophoretic buffer. The mass spectra were measured at m/z 51, 52 and 56 for V. Cr and Fe, respectively. The interfering polyatomic ions of 35Cl16O+, 40Ar12C+ and 40Ar16O+ on 51V+, 52Cr+ and 56Fe+ determination were reduced in intensity significantly by using NH3 as the reaction cell gas in the DRC. The detection limits were in the range of 0.1-0.5, 0.4-1.3 and 1.2-1.7 ng ml(-1) for V, Cr and Fe, respectively. Applications of the method for the speciation of V, Cr and Fe in wastewater were demonstrated. The recoveries were in the range of 92-120% for various species.

Chromium↗

Cloud point extraction for high-performance liquid chromatographic speciation of Cr(III) and Cr(VI) in aqueous solutions.

Cloud point extraction (CPE) was applied as a preconcentration step for HPLC speciation of chromium in aqueous solutions. Simultaneous preconcentration of Cr(III) and Cr(VI) in aqueous solutions was achieved by CPE with diethyldithiocarbamate (DDTC) as the chelating agent and Triton X-114 as the extractant. Baseline separation of the DDTC chelates of Cr(III) and Cr(VI) was realized on a RP-C18 column with the use of a mixture of methanol-water-acetonitrile (65:21:14, v/v) buffered with 0.05 M NaAc-HAc solution (pH 3.6) as the mobile phase at a flow rate of 1.0 ml min(-1). The precision (R.S.D.) for eight replicate injections of a mixture of 100 microg l(-1) of Cr(III) and Cr(VI) were 0.6 and 0.5% for the retention time, 4.1 and 4.6% for the peak area measurement, respectively. The concentration factor, which is defined as the concentration ratio of the analyte in the final diluted surfactant-rich extract ready for HPLC separation and in the initial solution, was 65 for Cr(III) and 19 for Cr(VI). The linear concentration range was from 50 to 1000 microg l(-1) for Cr(III) and 50-2000 microg l(-1) for Cr(VI). The detection limits of Cr(III) and Cr(VI) were 3.4 and 5.2 microg l(-1), respectively. The developed method was applied to the speciation of Cr(III) and Cr(VI) in snow water, river water, seawater and wastewater samples.

Chromatography, High Pressure Liquid↗

On-line coupling of flow injection displacement sorption preconcentration to high-performance liquid chromatography for speciation analysis of mercury in seafood.

A simple and cost-effective method for speciation analysis of trace mercury in seafood was developed by on-line coupling flow injection microcolumn displacement sorption preconcentration to high-performance liquid chromatography (HPLC) with UV detection. The methodology involved the presorption of the Cu-PDC (pyrrolidine dithiocarbamate) chelate onto a microcolumn packed with a cigarette filter sorbent, simultaneous preconcentration of Hg(II), methylmercury (MeHg), ethylmercury (EtHg), and phenylmercury (PhHg) onto the microcolumn through a displacement reaction with the presorbed Cu-PDC, and their subsequent elution from the microcolumn for on-line HPLC separation. Interferences from heavy metal ions with lower stability of their PDC chelates relative to Cu-PDC were minimized without the need of any masking agents. With the consumption of 4.0 ml of sample solution, the enrichment factors were about 80. The detection limits were 10-25 ng g(-1) (as Hg) in fresh tissue. Precision (R.S.D. (%), n = 5) ranged from 2 to 3% at the 500 microg l(-1) (as Hg) level. The developed technique was validated by analyzing a certified reference material (DORM-2, dogfish-muscle), and was shown to be useful for mercury speciation in real seafood samples.

Chromatography, High Pressure Liquid↗

Speciation of arsenic and selenium by capillary electrophoresis.

Capillary electrophoresis (CE) with direct UV detection, both on-capillary and with a high-sensitivity detection cell (HSDC), were used for the simultaneous determination of arsenite [As(III)], arsenate [As(V)], monomethylarsonic acid (MMA), dimethylarsinic acid (DMA), selenate [Se(VI)], selenite [Se(IV)], selenocystine (SeC), selenomethionine (SeM) and selenocystamine (SeCM). These anionic and cationic species were separated with negative separation voltage polarity in a capillary coated with poly(diallydimethylammonium chloride) (PDDAC). The background electrolyte (BGE) providing optimal separation was 15 mM phosphate buffer at pH 10.6. Arsenic and selenium species were detected at 195 and 200 nm, respectively. The limit of detection (LOD) values with on-capillary detection (75 microm i.d.) for the individual analytes were 1.02, 1.50, 1.08, 1.35, 19.5, 0.36, 0.32, 1.11 and 1.47 mg/L, respectively (expressed as arsenic or selenium). The method precision for peak area was from 2.1 to 3.4% relative standard deviation. HSDC was applied to increase the detection sensitivity and gave LOD improvement factors from 4.7 to 8.2, yielding LODs for the individual target analytes ranging from 0.049 to 2.38 mg/L. When the normal sample stacking mode was employed using a sample plug up to 4.6% of capillary volume, both the cationic and anionic analytes were stacked simultaneously with LOD improvement factors of 2.6-4.5 yielding LODs for the individual analytes ranging from 0.11 to 7.42 mg/L. The method was applied for the speciation of arsenic in sediment and determination of SeM in a selenium nutrition supplement. The achieved separation selectivity also gives the method a more general application potential for simultaneous arsenic and selenium speciation when hyphenated with inductively coupled plasma MS.

Arsenic↗

High-performance liquid chromatography-ultrasonic nebulizer high-power nitrogen microwave-induced plasma mass spectrometry, real-time on-line coupling for selenium speciation analysis.

The coupling of a high-power nitrogen (N2) microwave-induced plasma (MIP) mass spectrometry--(MS) (1.3 kW) with high-performance liquid chromatography, connected with concentric nebulizer (CN), ultrasonic nebulizer (USN) and a hydride generation (HG) systems, for the optimization and determination of selenium compounds, has been carried out. The MIP-MS system fulfils the ideal requirement being an on-line real-time chromatographic detector for Se speciation analysis. Interchanging of MIP-MS system fabricated nebulizer (concentric) with an ultrasonic nebulizer increases about 3.4-12 (peak height) and 6.5-10 (peak area) times ion signals for the selenium compounds. The detection limits for selenate, selenite, trimethylselenonium ion (TmSe), selenomethionine (Semet) and selenoethionine (Seet) (in Milli-Q-water) obtained with the optimized HPLC-USN-N2MIP-MS system are 0.11, 0.14, 0.09, 0.14 and 0.10 microg L(-1), respectively, about 12-48 times lower than the HPLC-CN-MIP-MS and 1.5-4.4 (peak height) times lower compared to the HPLC-CN-inductively coupled plasma (ICP)-MS coupling. Considering peak area, the repeatability (R.S.D. for three successive analyses) and intermediate precision (R.S.D. for three successive analyses performed on three different days), achieved for five Se compounds are 0.8-5.6, and 1.1-5.9%, comparable with the HPLC-CN-ICP-MS, HPLC-HG-MIP-MS and HPLC-CN-MIP-MS systems. The combined HPLC-USN-N2MIP-MS has been adequately applied for the determination of Se compounds in certified National Institute for Environmental studies human urine CRM No. 18. The results reasonably agree with the HPLC-CN-ICP-MS values. This encouraging combination may be an alternative ion source of mass spectrometry for coming generation in regard to the selenium speciation analysis.

Chromatography, High Pressure Liquid↗

Arsenic and its speciation analysis using high-performance liquid chromatography and inductively coupled plasma mass spectrometry.

It is known that arsenic has different toxicological properties dependent upon both its oxidation state for inorganic compounds, as well as the different toxicity levels exhibited for organic arsenic compounds. The field of arsenic speciation analysis has grown rapidly in recent years, especially with the utilization of high-performance liquid chromatography (HPLC) coupled to inductively coupled plasma mass spectrometry (ICP-MS), a highly sensitive and robust detector system. Complete characterization of arsenic compounds is necessary to understand intake, accumulation, transport, storage, detoxification and activation of this element in the natural environment and living systems. This review describes the essential background and toxicity of arsenic in the environment, and more importantly, some currently used chromatographic applications and sample handling procedures necessary to accurately detect and quantify arsenic in its various chemical forms. Applications and work using only HPLC-ICP-MS for arsenic speciation of environmental and biological samples are presented in this review.

Arsenic↗

Selenium speciation analysis using inductively coupled plasma-mass spectrometry.

Selenium exists in several oxidation states and a variety of inorganic and organic compounds, and the chemistry of selenium is complex in both the environment and living systems. Selenium is an essential element at trace levels and toxic at greater levels. Interest in speciation analysis for selenium has grown rapidly in this last decade, especially in the use of chromatographic separation coupled with inductively coupled plasma-mass spectrometry (ICP-MS). Complete characterization of selenium compounds is necessary to understand selenium's significance in metabolic processes, clinical chemistry, biology, toxicology, nutrition and the environment. This review describes some of the essential background of selenium, and more importantly, some of the currently used separation methodologies, both chromatographic and electrophoretic, with emphasis on applications of selenium speciation analysis using ICP-MS detection.

Chromatography, Gas↗

Influence of hydrology on heavy metal speciation and mobility in a Pb-Zn mine tailing.

Among the inorganic toxicants of greatest concern in mine tailings, Pb, Zn, Cu, Cd and As figure prominently due to their abundance and potential toxicity. Here we report on their biolability and solid-phase speciation in two sediment cores subject to variable hydrological regimes at an abandoned pyritic mine tailing. The oxic conditions of well-drained sediments induced pyrite oxidation and the subsequent liberation of H+, SO4(2-) and considerable quantities of Fe(III), which precipitated as goethite. Solubility of Pb, Zn, Cu and Cd was closely coupled to pH and goethite presence. Metal lability was particularly low in zones of neutralization, formed by the accumulation of calcite, first carried then deposited by percolating waters in both saturated and unsaturated cores. We conclude that differential hydrology induces variable heavy metal speciation and biolability in Pb-Zn mine tailings, and suggest that site-specific risk assessments must account for past and present hydrological regimes.

Biological Availability↗

Initial steps of speciation by geographic isolation and host switch in salmonid pathogen Gyrodactylus salaris (Monogenea: Gyrodactylidae).

To test the hypothesis that host-switching can be an important step in the speciation of gyrodactylid monogenean flatworms, we inferred the phylogeny within a cluster of parasites morphologically close to Gyrodactylus salaris Malmberg 1957, collected from Atlantic, Baltic and White Sea salmon (Salmo salar), farmed rainbow trout (Oncorhynchus mykiss), and grayling (Thymallus thymallus) from Northern Europe. The internal transcribed spacer region of the nuclear ribosomal gene was sequenced for taxonomic identification. Parasites on grayling from the White Sea Basin differed from the others by one nucleotide (0.08%), the remainder were identical to the sequence published earlier from Norway (G. salaris on salmon), England (Gyrodactylus thymalli on grayling), and the Czech Republic (unidentified salaris/thymalli on trout). For increased resolution, 813 nucleotides of the mitochondrial COI gene of 88 parasites were sequenced and compared with 76 published sequences using phylogenetic analysis. For all tree building algorithms (NJ, MP), the parasites formed a star-like phylogeny of six definite sister clades, indicating nearly simultaneous radiation. Average K2P distances between clades were 1.8-2.6%, and internal mean distances 0.2-1.1%. The genetic distance to the nearest known relative, Gyrodactylus lavareti Malmberg, was 24%. A variable salmon-specific mitochondrial Clade I was observed both in the Baltic Basin and in pathogenic populations introduced to the Atlantic and White Sea coasts. An invariable Clade II was common in rainbow trout farms in Sweden, Denmark and Finland; the same haplotype was also infecting salmon in a landlocked population in Russian Karelia, and in Oslo fjord and Sognefjord in Norway. Four geographically vicariant sister clades were observed on graylings: Clade III in the Baltic Sea Basin; Clade IV in Karelian rivers draining to the White Sea; Clade V in Norwegian river draining to Swedish lake Vänern; and Clade VI in rivers draining to Oslo fjord. The pattern fitted perfectly with the postglacial history of grayling distribution. Widely sampled clades from salmon and Baltic grayling had basal haplotypes in populations, which were isolated early during the postglacial recolonisation. The divergence between the six clades was clear and linked with their hosts, but not wide enough to support a species status for them. Parasites from the Slovakian type population of G. thymalli were not available, so this result does not mean that G. salaris and G. thymalli are synonyms. It is suggested that the plesiomorphic host of the parasite cluster was grayling, and the switch to salmon occurred at least once when the continental ice isolated Baltic salmon in an eastern freshwater refugium, 130,000 years ago. At the same time, parasites on grayling were split geographically and isolated into several allopatric refugia. The divergence among the parasite clades allowed a tentative calibration of the evolutionary rate, leading to an estimate of the divergence of 13.7-20.3% per million years for COI coding mtDNA. The results supported the hypothesis that parallel to the allopatric mode, host switch and instant isolation by host specificity can be operated as a speciation mechanism.

Amino Acid Sequence↗

Use of analytical microscopy to analyze the speciation of copper and chromium ions onto a low-cost biomaterial.

In this paper, we present our study of the speciation of copper and hexavalent chromium sorbed onto a lignocellulosic substrate, using analytical microscopy. The lignocellulosic substrate constitutes a low-cost biomaterial that can be used in wastewater treatment. Transmission electron microscopy (TEM) coupled with energy-dispersive X-ray spectroscopy (EDXS) was used to determine the speciation of the two metal ions on the constitutive moieties of the lignocellulosic substrate. The use of a staining agent sensitive to carbon unsaturation allowed us to differentiate between the microstructures rich in lignin entities and those rich in cellulose entities. The EDX analysis showed that metal ions are preferentially sorbed onto microstructures rich in lignin moieties. The energy electron loss spectroscopy (EELS) was used to determine the oxidation states of chromium in association with lignocellulosic moieties. We showed that the sorption process of hexavalent chromium requires the reduction of Cr(VI) into Cr(III) and the probable oxidation of lignin moieties.

Cellulose↗

Surface speciation of As(III) and As(V) in relation to charge distribution.

The adsorption of As(III) and As(V) on goethite has been studied as a function of pH and loading. The data can be successfully described with the charge distribution (CD) model (extended Stern layer option) using realistic species observed by EXAFS. The CD values have been derived theoretically. Therefore, the Brown bond valence approach has been applied to MO/DFT optimized geometries of a series of hydrated complexes of As(III) and As(V) with Fe(III) (hydr)oxide. The calculated ionic CD values have been corrected for the effect of dipole orientation of interfacial water, resulting in overall interfacial CD coefficients that can be used to describe the surface speciation as a function of pH and loading. For As(III), the main surface species is a bidentate complex and a minor contribution of a monodentate species is found, which is in agreement with EXAFS. The CD values have also been fitted. Such an analysis of the adsorption data resulted in the same surface species. The fitted CD values for the bidentate complex points to the presence of strong AsO bonds with the surface and a weaker AsOH bond with the free OH ligand. This agrees quantitatively with the MO/DFT optimized geometry. Interpretation of free fitted CD values for As(V) binding suggests that the main surface species is a non-protonated bidentate complex (B) with a contribution of a singly protonated surface complex (MH) at sub-neutral pH and high loading. In addition, a protonated bidentate surface complex (BH) may be present. The same species are found if the theoretical CD values are used in the data analysis. The pH dependency of surface speciation is strongly influenced by the charge attribution of adsorbed species to the electrostatic surface plane while the effect of loading is primarily controlled by the amount of charge attributed to the 1-plane, illustrating the different action of the CD value. The MO/DFT geometry optimizations furthermore suggest that for As(V) the B, MH and BH surface complexes may have very similar AsFe distances which may complicate the interpretation of EXAFS data.

Adsorption↗

Radionuclide speciation and its relevance in environmental impact assessments.

To assess the long-term environmental impact of radioactive contamination of ecosystems, information on source terms including radionuclide speciation, mobility and biological uptake is needed. A major fraction of refractory radionuclides released from nuclear sources such as nuclear weapons tests and reactor accidents is present as radioactive particles, whilst radionuclides are also present as colloids or low molecular mass species in effluents from nuclear installations. Low molecular mass species are more mobile (lower apparent K(d)) and bioavailable (higher apparent BCF) than colloids and particles. Soils and sediments act as sinks for particles and colloids. Due to particle weathering, associated radionuclides can be remobilised over time. Thus, information on particle characteristics such as composition, particle size, crystalline structures and oxidation states influencing weathering rates and subsequent mobilisation is essential. The present article summarises current knowledge on radioactive particles released from different sources, and the relevance of radionuclide speciation for mobility and biological uptake.

Colloids↗

Solid/solution partitioning and speciation of heavy metals in the contaminated agricultural soils around a copper mine in eastern Nanjing city, China.

Solid/solution partition coefficient (Kd) and speciation of soil heavy metals can be used for predicting their environmental risks. The Kd values and solution speciation of soil Cu, Cd and Zn were analyzed in 40 samples of contaminated agricultural soils around Jiuhua copper mine in eastern Nanjing city, China. The Kd ranges (and mean values) for soil Cu, Cd and Zn are 703-7418 (3453), 37.3-3963 (940) and 319-17965 (7244) L kg-1, respectively, showing a large variability both for metals and soils. The results of differential pulse anodic stripping voltammetry (DPASV) indicates that 95.6% solution Cu is bound to dissolved organic ligands. About half of the dissolved Zn is DPASV-labile at pH<6, while 92.1% solution Zn is in the form of organic complexes at pH>6. DPASV-labile Cd is ranged from 22.6 to 98.7% with the mean value of 56.3%. Multiple linear regressions indicate that Kd, the dissolved and DPASV-labile concentrations of Cd and Zn are mostly influenced by the soil solution pH with R2 of 0.50, 0.59 and 0.63, respectively for Cd, and 0.58, 0.72 and 0.64, respectively for Zn. Considering the second parameter of corresponding soil metal, the linear relationships of Kd with pH were improved with R2 of 0.70 and 0.73 for Cd and Zn, respectively. However, the solubility of soil Cu was insensitive to pH. Only SOC shows a weak relationship to the dissolved Cu with R2 of 0.21. As for its Kd, total soil Cu is the most significant factor. But for DPASV-labile Cu, no soil parameters were found to be good predictors.

Agriculture↗