A Comparative Study on the Sorption Characteristics of Pb(II and Hg(II onto Activated Carbon

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N. Muthulakshmi Andal

2010-01-01

Full Text Available Biosorption equilibrium and kinetics of Pb(II and Hg(II on coconut shell carbon (CSC were investigated by batch equilibration method. The effects of pH, adsorbent dosage, contact time, temperature and initial concentration of Pb(II and Hg(II on the activated carbon of coconut shell wastes were studied. Maximum adsorption of Pb(II occurred at pH 4.5 and Hg(II at pH 6. The sorptive mechanism followed the pseudo second order kinetics. The equilibrium data were analysed by Langmuir, Freundlich and Dubinin-Radushkevich isotherm models. The equilibration data fitted well with both Langmuir and Freundlich isotherm model. The Langmuir adsorption capacity for Pb(II was greater than Hg(II. The mean free energy of adsorption calculated from Dubinin-Radushkevich (D-R isotherm model indicated that the adsorption of metal ions was found to be by chemical ion exchange. Thermodynamic parameter showed that the sorption process of Pb(II onto SDC was feasible, spontaneous and endothermic under studied conditions. A comparison was evaluated for the two metals.

Evaluation of heavy metals (Cr, Fe, Ni, Cu, Zn, Cd, Pb and Hg) in water, sediments and water lily (Eichornia crassipes) from Jose Antonio Alzate dam; Evaluacion de metales pesados Cr, Fe, Ni, Cu, Zn, Cd, Pb y Hg en agua, sedimento y lirio acuatico (Eichhornia crassipes) de la Presa Jose Antonio Alzate, Estado de Mexico

Energy Technology Data Exchange (ETDEWEB)

Avila P, P

1996-12-31

Water, sediments and water lily (Eichornia crassipes) from the Jose Antonio Alzate Dam were analyzed in order to determine concentrations of chromium, iron, nickel, copper, zinc, cadmium, lead and mercury. Mercury, lead, chromium and iron were found in concentrations above permissible limits in water, and in high concentrations in sediments. Cadmium, nickel, copper and zinc never were found in concentrations above permissible limits in water. The highest concentrations of heavy metals in water lily were found in the root. Accumulation factors decreased in the following order: Zn> Cr> Fe> Ni> Cu> Pb> Hg and Cd. Statistical differences ({alpha} < 0.5) between the collection samples dates was observed. High correlations between metals concentrations in superficial water, sediment and water hyacinth were also observed. These correlations could indicate that the heavy metals studied here, are originated from a natural source such as sediments or from an industrial source. (Author).

Evaluation of heavy metals (Cr, Fe, Ni, Cu, Zn, Cd, Pb and Hg) in water, sediments and water lily (Eichornia crassipes) from Jose Antonio Alzate dam

International Nuclear Information System (INIS)

Avila P, P.

1995-01-01

Water, sediments and water lily (Eichornia crassipes) from the Jose Antonio Alzate Dam were analyzed in order to determine concentrations of chromium, iron, nickel, copper, zinc, cadmium, lead and mercury. Mercury, lead, chromium and iron were found in concentrations above permissible limits in water, and in high concentrations in sediments. Cadmium, nickel, copper and zinc never were found in concentrations above permissible limits in water. The highest concentrations of heavy metals in water lily were found in the root. Accumulation factors decreased in the following order: Zn> Cr> Fe> Ni> Cu> Pb> Hg and Cd. Statistical differences (α < 0.5) between the collection samples dates was observed. High correlations between metals concentrations in superficial water, sediment and water hyacinth were also observed. These correlations could indicate that the heavy metals studied here, are originated from a natural source such as sediments or from an industrial source. (Author)

Biokinetics of Hg and Pb accumulation in the encapsulated egg of the common cuttlefish Sepia officinalis: Radiotracer experiments

International Nuclear Information System (INIS)

Lacoue-Labarthe, T.; Warnau, M.; Metian, M.; Oberhaensli, F.; Rouleau, C.; Bustamante, P.

2009-01-01

Uptake and depuration kinetics of dissolved 203 Hg and 210 Pb were determined during the entire embryonic development of the eggs of the cuttlefish, Sepia officinalis (50 d at 17 o C). 203 Hg and 210 Pb were accumulated continuously by the eggs all along the development time reaching load/concentration ratio (LCR) of 467 ± 43 and 1301 ± 126 g, respectively. During the first month, most of the 203 Hg and 210 Pb remained associated with the eggshell indicating that the latter acted as an efficient shield against metal penetration. From this time onwards, 203 Hg accumulated in the embryo, indicating that it passed through the eggshell, whereas 210 Pb did not cross the chorion during the whole exposure time. It also demonstrated that translocation of Hg associated with the inner layers of the eggshell is a significant source of exposure for the embryo. This study highlighted that the maturing embryo could be subjected to the toxic effects of Hg in the coastal waters where the embryonic development is taking place.

Biokinetics of Hg and Pb accumulation in the encapsulated egg of the common cuttlefish Sepia officinalis: Radiotracer experiments

Energy Technology Data Exchange (ETDEWEB)

Lacoue-Labarthe, T., E-mail: tlacouel@gmail.com [Littoral, Environnement et Societes (LIENSs), UMR 6250, CNRS-Universite de La Rochelle, 2 rue Olympe de Gouges, F-17042 La Rochelle Cedex 01 (France); Warnau, M., E-mail: warnaumichel@yahoo.com [International Atomic Energy Agency - Marine Environment Laboratories, 4 Quai Antoine Ier, MC-98000 (Monaco); Metian, M. [Littoral, Environnement et Societes (LIENSs), UMR 6250, CNRS-Universite de La Rochelle, 2 rue Olympe de Gouges, F-17042 La Rochelle Cedex 01 (France); International Atomic Energy Agency - Marine Environment Laboratories, 4 Quai Antoine Ier, MC-98000 (Monaco); Oberhaensli, F. [International Atomic Energy Agency - Marine Environment Laboratories, 4 Quai Antoine Ier, MC-98000 (Monaco); Rouleau, C. [Institut Maurice-Lamontagne, 850 Route de la Mer, C.P. 1000, Mont-Joli, Quebec (Canada); Bustamante, P., E-mail: pbustama@univ-lr.fr [Littoral, Environnement et Societes (LIENSs), UMR 6250, CNRS-Universite de La Rochelle, 2 rue Olympe de Gouges, F-17042 La Rochelle Cedex 01 (France)

2009-12-01

Uptake and depuration kinetics of dissolved {sup 203}Hg and {sup 210}Pb were determined during the entire embryonic development of the eggs of the cuttlefish, Sepia officinalis (50 d at 17 {sup o}C). {sup 203}Hg and {sup 210}Pb were accumulated continuously by the eggs all along the development time reaching load/concentration ratio (LCR) of 467 {+-} 43 and 1301 {+-} 126 g, respectively. During the first month, most of the {sup 203}Hg and {sup 210}Pb remained associated with the eggshell indicating that the latter acted as an efficient shield against metal penetration. From this time onwards, {sup 203}Hg accumulated in the embryo, indicating that it passed through the eggshell, whereas {sup 210}Pb did not cross the chorion during the whole exposure time. It also demonstrated that translocation of Hg associated with the inner layers of the eggshell is a significant source of exposure for the embryo. This study highlighted that the maturing embryo could be subjected to the toxic effects of Hg in the coastal waters where the embryonic development is taking place.

Distribution of toxic metals, Hg, Cd and Pb in zooplankton along the Indian coasts

Digital Repository Service at National Institute of Oceanography (India)

Sengupta, R.; Kureishy, T.W.

Distribution of toxic metals such as Hg, Cd and Pb in zooplankton is assessed with a view to correlate it with the prevalent environmental conditions along the Indian coast. While Hg could not be detected in zooplankton the concentrations of Cd...

Assessment of Individual and Combined Toxicities of Four Non-Essential Metals (As, Cd, Hg and Pb in the Microtox Assay

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Paul B. Tchounwou

2006-03-01

Full Text Available Although most researches with non-essential metals (NEMs have been done with single or individual metals, in reality, organisms are often exposed to multiple contaminants at the same time through the air, food and water. In this study, we tested the toxicity of four NEMs, As, Cd, Pb, and Hg, individually and as a composite mixture using the microtox bioassay. This assay uses the reduction of bioluminescence of the bacterium Vibrio fischeri as a measure of toxicity. The concentrations of each chemical in the mixture were based on multiples of their maximum contaminant levels (MCLs set by the U.S. EPA. The highest concentration of exposure was 20 times the MCL, which translated into 200, 100, 40 and 300 ppb for As, Cd, Hg and Pb, respectively. The ratio for the mixture from these concentrations was 10:5:2:15 for As, Cd, Hg and Pb, respectively. Among the individual metals tested, the ranking of toxicity was Hg>Pb>Cd>As based on the EC50 values of 109, 455, 508 and 768 ppb for Hg, Pb, Cd and As, respectively. The EC50 for the composite mixture was 495% MCL which translated into nominal concentrations of 49, 25, 10 and 74 ppb for As, Cd, Hg, and Pb, respectively. Overall, the EC50 value of each NEM within the mixture was lower than the EC50 of the individual chemical; an evidence of synergism for the mixture. The individual toxic units (TU were 0.06, 0.05, 0.09, and 0.16 for As, Cd Hg, and Pb, respectively and the summed toxic unit (TU was 0.37 (less than 1. This study provides needed scientific data necessary for carrying out complete risk assessment of As, Cd, Hg, and Pb mixtures of some priority compounds.

The use of Pb, Sr, and Hg isotopes in Great Lakes precipitation as a tool for pollution source attribution

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Sherman, Laura S., E-mail: lsaylors@umich.edu [University of Michigan, Department of Earth and Environmental Sciences, 1100 N. University Ave., Ann Arbor, MI 48109 (United States); Blum, Joel D. [University of Michigan, Department of Earth and Environmental Sciences, 1100 N. University Ave., Ann Arbor, MI 48109 (United States); Dvonch, J. Timothy [University of Michigan, Air Quality Laboratory, 1415 Washington Heights, Ann Arbor, MI 48109 (United States); Gratz, Lynne E. [University of Washington-Bothell, 18115 Campus Way NE, Bothell, WA 98011 (United States); Landis, Matthew S. [U.S. EPA, Office of Research and Development, Research Triangle Park, NC 27709 (United States)

2015-01-01

The anthropogenic emission and subsequent deposition of heavy metals including mercury (Hg) and lead (Pb) present human health and environmental concerns. Although it is known that local and regional sources of these metals contribute to deposition in the Great Lakes region, it is difficult to trace emissions from point sources to impacted sites. Recent studies suggest that metal isotope ratios may be useful for distinguishing between and tracing source emissions. We measured Pb, strontium (Sr), and Hg isotope ratios in daily precipitation samples that were collected at seven sites across the Great Lakes region between 2003 and 2007. Lead isotope ratios ({sup 207}Pb/{sup 206}Pb = 0.8062 to 0.8554) suggest that Pb deposition was influenced by coal combustion and processing of Mississippi Valley-Type Pb ore deposits. Regional differences in Sr isotope ratios ({sup 87}Sr/{sup 86}Sr = 0.70859 to 0.71155) are likely related to coal fly ash and soil dust. Mercury isotope ratios (δ{sup 202}Hg = − 1.13 to 0.13‰) also varied among the sites, likely due to regional differences in coal isotopic composition, and fractionation occurring within industrial facilities and in the atmosphere. These data represent the first combined characterization of Pb, Sr, and Hg isotope ratios in precipitation collected across the Great Lakes region. We demonstrate the utility of multiple metal isotope ratios in parallel with traditional trace element multivariate statistical modeling to enable more complete pollution source attribution. - Highlights: • We measured Pb, Sr, and Hg isotopes in precipitation from the Great Lakes region. • Pb isotopes suggest that deposition was impacted by coal combustion and metal production. • Sr isotope ratios vary regionally, likely due to soil dust and coal fly ash. • Hg isotopes vary due to fractionation occurring within facilities and the atmosphere. • Isotope results support conclusions of previous trace element receptor modeling.

Water Soluble Cationic Porphyrin Sensor for Detection of Hg2+, Pb2+, Cd2+, and Cu2+

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Matibur Zamadar

2016-01-01

Full Text Available Here we report the sensing properties of the aqueous solution of meso-tetra(N-methyl-4-pyridylporphine tetrachloride (1 for simultaneous detection of toxic metal ions by using UV-vis spectroscopy. Cationic porphyrin 1 displayed different electronic absorptions in UV-vis region upon interacting with Hg2+, Pb2+, Cd2+, and Cu2+ ions in neutral water solution at room temperature. Quite interestingly, the porphyrin 1 showed that it can function as a single optical chemical sensor and/or metal ion receptor capable of detecting two or more toxic metal ions, particularly Hg2+, Pb2+, and Cd2+ ions coexisting in a water sample. Porphyrin 1 in an aqueous solution provides a unique UV-vis sensing system for the determination of Cd2+ in the presence of larger metal ions such as Hg2+, or Pb2+. Finally, the examination of the sensing properties of 1 demonstrated that it can operate as a Cu2+ ion selective sensor via metal displacement from the 1-Hg2+, 1-Pb2+, and 1-Cd2+.

Hg, Pb and Cd in zooplankton from an area of the Adriatic opposite the Romagna coast line

Energy Technology Data Exchange (ETDEWEB)

Crisetig, G; Cattani, O; Massa, D; Poletti, R

1982-09-15

The concentrations of heavy metals Hg, Pb and Cd found in zooplankton samples collected in two stations off Cesenatico (Northern Adriatic Sea) from March 1978 to January 1979, have been reported. The Hg, Pb and Cd concentrations showed large variations which did not seem to be correlated with taxonomic composition. The detected levels of metals were higher at the offshore than the nearshore station, accordingly with the sediment pattern. The high concentration of Hg were apparently associated with sources of local industrial pollution.

Biomonitoring potential of five sympatric Tillandsia species for evaluating urban metal pollution (Cd, Hg and Pb)

Science.gov (United States)

Sánchez-Chardi, Alejandro

2016-04-01

The present study quantifies non essential heavy metals highly toxic for biological systems (Pb, Hg and Cd) in five autochthonous epiphytic plants from Tillandsia genus (T. recurvata, T. meridionalis, T. duratii, T. tricholepis, T. loliacea) according to different traffic levels (reference, low, medium and high polluted sites) in Asunción (Paraguay). The three metals increased in polluted sites following Pb (till 62.99 ppm in T. tricholepis) > Cd (till 1.35 ppm in T. recurvata) > Hg (till 0.36 ppm in T. recurvata) and Pb and Cd levels were directly related to traffic flow. Although the species showed similar bioaccumulation pattern (namely, higher levels of metals in polluted sites), enrichment factors (maximum EF values 37.00, 18.16, and 11.90 for Pb, Hg, and Cd, respectively) reported T. tricholepis as the most relevant bioindicator due to its wide distribution and abundance in study sites, low metal content in control site and high metal contents in polluted sites, and significant correlations with traffic density of Pb and Cd. This study emphasizes the necessity of biomonitoring air pollution in areas out of air monitoring control such as Asunción, where the high levels of metal pollution especially Pb, may represent an increment of risk for the human population inhabiting this urban area.

Phytoremediation of Pb and Hg by using Scirpus mucronatus with addition of bacterial inoculums

International Nuclear Information System (INIS)

Hamzah, A.; Yatim, N.I.; Sarmani, S.B.

2015-01-01

Two heavy metal-resistant rhizobacteria bacteria (Brevundimonas diminuta SF-S1-5 and Alcaligenes faecalis SF-S1-60) were bioaugmented in sand and also spiked with 100 ppm Pb and 1 ppm Hg and the removal of these metals was monitored using plant, Scirpus mucronatus. The highest accumulation of Pb and Hg were obtained in the root of S. mucronatus inoculated with A. faecalis at day 42 and 28, respectively. Plant inoculated with A. faecalis also showed the highest bioaccumulation coefficient and bioconcentration factor values > 1 compared to plant inoculated with B. diminuta and control. (author)

Chemical speciation of Pb(II, Cd(II, Hg(II, Co(II, Ni(II, Cu(II and Zn(II binary complexes of l-methionine in 1,2-propanediol-water mixtures

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M. Padma Latha

2007-04-01

Full Text Available Chemical speciation of Pb(II, Cd(II, Hg(II, Co(II, Ni(II, Cu(II and Zn(II complexes of L-methionine in 0.0-60 % v/v 1,2-propanediol-water mixtures maintaining an ionic strength of 0.16 M at 303 K has been studied pH metrically. The active forms of ligand are LH2+, LH and L-. The predominant species detected are ML, MLH, ML2, ML2H, ML2H2 and MLOH. Models containing different numbers of species were refined by using the computer program MINIQUAD 75. The best-fit chemical models were arrived at based on statistical parameters. The trend in variation of complex stability constants with change in the dielectric constant of the medium is explained on the basis of electrostatic and non-electrostatic forces.

Tolerance and hyperaccumulation of a mixture of heavy metals (Cu, Pb, Hg, and Zn) by four aquatic macrophytes.

Science.gov (United States)

Romero-Hernández, Jorge Alberto; Amaya-Chávez, Araceli; Balderas-Hernández, Patricia; Roa-Morales, Gabriela; González-Rivas, Nelly; Balderas-Plata, Miguel Ángel

2017-03-04

In the present investigation, four macrophytes, namely Typha latifolia (L.), Lemna minor (L.), Eichhornia crassipes (Mart.) Solms-Laubach, and Myriophyllum aquaticum (Vell.) Verdc, were evaluated for their heavy metal (Cu, Pb, Hg, and Zn) hyperaccumulation potential under laboratory conditions. Tolerance analyses were performed for 7 days of exposure at five different treatments of the metals mixture (Cu +2 , Hg +2 , Pb +2 , and Zn +2 ). The production of chlorophyll and carotenoids was determined at the end of each treatment. L. minor revealed to be sensitive, because it did not survive in all the tested concentrations after 72 hours of exposure. E. crassipes and M. aquaticum displayed the highest tolerance to the metals mixture. For the most tolerant species of aquatic macrophytes, The removal kinetics of E. crassipes and M. aquaticum was carried out, using the following mixture of metals: Cu (0.5 mg/L) and Hg, Pb, and Zn 0.25 mg/L. The obtained results revealed that E. crassipes can remove 99.80% of Cu, 97.88% of Pb, 99.53% of Hg, and 94.37% of Zn. M. aquaticum withdraws 95.2% of Cu, 94.28% of Pb, 99.19% of Hg, and 91.91% of Zn. The obtained results suggest that these two species of macrophytes could be used for the phytoremediation of this mixture of heavy metals from the polluted water bodies.

Exotic Earthworms Decrease Cd, Hg, and Pb Pools in Upland Forest Soils of Vermont and New Hampshire USA.

Science.gov (United States)

Richardson, J B; Görres, J H; Friedland, A J

2017-10-01

Exotic earthworms are present in the forests of northeastern USA, yet few studies have documented their effects on pollutant metals in soil. The objective of this study was to identify if Cd, Hg, and Pb strong-acid extractable concentrations and pools (bulk inventories) in forest soils decreased with the presence of exotic earthworms. We compared 'Low Earthworm Abundance' (LEA) sites (≤10 g m -2 earthworms, n = 13) and 'High Earthworm Abundance' (HEA) (>10 g m -2 earthworms, n = 17) sites at five watersheds across Vermont and New Hampshire. Organic horizon Cd, Hg, and Pb concentrations were lower at HEA than LEA sites. Organic horizon and total soil pools of Cd and Hg were negatively correlated with earthworm biomass. Soil profile Cd and Hg concentrations were lower at HEA than LEA sites. Our results suggest earthworms are decreasing accumulation of Cd, Hg, and Pb in forest soils, potentially via greater mobilization through organic matter disruption or bioaccumulation.

Determination of Fe, Hg, Mn, and Pb in three-rings of poplar (Populus alba L.) by U-shaped DC arc

Science.gov (United States)

Marković, D. M.; Novović, I.; Vilotić, D.; Ignjatović, Lj.

2007-09-01

The U-shaped DC arc with aerosol supply was applied for the determination of Fe, Hg, Mn, and Pb in poplar (Populus alba L.) tree-rings. By optimization of the operating parameters and by selection of the most appropriate signal integration time (20 s for Fe, Mn, and Pb and 30 s for Hg), the obtained limits of detection for Fe, Hg, Mn, and Pb are 5.8, 2.6, 1.6, and 2.0 ng/ml, respectively. The detection limits achieved by this method for Fe, Hg, Mn, and Pb are comparable with the detection limits obtained for these elements by such methods as inductively coupled plasma-atomic emission spectrometry (ICP-AES), direct coupled plasmatomic emission spectrometry (DCP-AES), and microwave-induced plasma-atomic emission spectrometry (MIP-AES). We used the tree-rings of poplar from two different locations. The first one is in the area close to the power plant “Nikola Tesla” TENT A, Obrenovac, while the other one is in the urban area of Novi Sad. In almost all cases, samples from the location at Obrenovac registered elevated average concentrations of Fe, Hg, Mn, and Pb in the tree-rings of poplar.

Pb(II) and Hg(II) binding to $\\textit{de novo}$ designed proteins studied by $^{204m}$Pb- and $^{199m}$Hg-Perturbed Angular Correlation of $\\gamma$-rays (PAC) spectroscopy : Clues to heavy metal toxicity

CERN Multimedia

2002-01-01

$\\textit{De novo}$ design of proteins combined with PAC spectroscopy offers a unique and powerful approach to the study of fundamental chemistry of heavy metal-protein interactions, and thus of the mechanisms underlying heavy metal toxicity. In this project we focus on Pb(II) and Hg(II) binding to designed three stranded coiled coil proteins with one or two binding sites, mimicking a variety of naturally occurring thiolate-rich metal ion binding sites in proteins. The $^{204m}$Pb- and $^{199m}$Hg-PAC experiments will complement data already recorded with EXAFS, NMR, UV-Vis and CD spectroscopies.

Quijarroite, Cu6HgPb2Bi4Se12, a New Selenide from the El Dragόn Mine, Bolivia

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Hans-Jürgen Förster

2016-11-01

Full Text Available Quijarroite, ideally Cu6HgPb2Bi4Se12, is a new selenide species from the El Dragόn mine, Department of Potosí, Bolivia. It most frequently occurs as lath-shaped thin plates (up to 150 µm in length and 20 µm in width intimately (subparallel intergrown with hansblockite, forming an angular network-like intersertal texture. Quijarroite is occasionally also present as sub- to anhedral grains up to 200 µm in length and 50 µm in width. It is non-fluorescent, black and opaque with a metallic luster and black streak. It is brittle, with an irregular fracture and no obvious cleavage and parting. In plane-polarized incident light, quijarroite is weakly pleochroic from cream to very slightly more brownish-cream, displaying no internal reflections. Between crossed polars, quijarroite is moderately anisotropic with pale orange-brown to blue rotation tints. Lamellar twinning on {110} is common; parquet twinning occurs rarely. The reflectance values in the air for the COM (Commission on Ore Mineralogy standard wavelengths (R1 and R2 are: 46.7, 46.8 (470 nm, 47.4, 48.2 (546 nm, 47.1, 48.5 (589 nm, and 46.6, 48.7 (650 nm. Electron-microprobe analyses yielded a mean composition of Cu 13.34, Ag 1.02, Hg 7.67, Pb 16.87, Co 0.03, Ni 0.15, Bi 27.65, Se 33.52, total 100.24 wt %. The mean empirical formula, normalized to 25 apfu (atoms per formula unit, is (Cu5.84Ag0.26Σ = 6.10(Hg1.06Ni0.07Co0.01Σ = 1.14Pb2.27Bi3.68Se11.81 (n = 24. The simplified formula is Cu6HgPb2Bi4Se12. Quijarroite is orthorhombic, space group Pmn21, with a = 9.2413(8, b = 9.0206(7, c = 9.6219(8 Å, V = 802.1(1 Å3, Z = 1. The calculated density is 5.771 g·cm−3. The five strongest X-ray powder-diffraction lines (d in Å (I/I0 (hkl are: 5.36 (55 (111, 3.785 (60 (211, 3.291 (90 (022, 3.125 (100 (212, and 2.312 (50 (400. The crystal structure of quijarroite can be considered a galena derivative and could be derived from that of bournonite. It is a primary mineral, deposited from an

Ecological effects of some heavy metals (Cd, Pb, Hg, Cr) pollution of ...

African Journals Online (AJOL)

STORAGESEVER

2008-06-17

Jun 17, 2008 ... Accumulation of heavy metals (Cd, Pb, Hg, Cr) in water and plankton of Sarıyar Dam Lake (SDR) was seasonally ... human impacts in protected areas with the aim of .... (1999), heavy metals toxicity is affected by temperature,.

Eco-toxicology effect on Moina mongolica Daday exposed to Cd2+, Pb2+, and Hg2+ by the food chain.

Science.gov (United States)

Wang, Meiru; Zhao, Wen; Jia, Xuying; Wei, Jie; Wang, Shan

2018-03-28

As one of the most important contaminants, heavy metals can seriously influence human health via the food chain. In this study, the eco-toxicological effects of Cd 2+ , Pb 2+ , and Hg 2+ on Moina mongolica Daday were investigated by feeding them Chlorella sp. that contained heavy metals. The relative body lengths of the M. mongolica changed rapidly, peaking at 2 days for Hg 2+ , 6 days for Cd 2+ , and 8 days for Pb 2+ . Moreover, grazing and clearance rates of the experimental group were apparently lower than those of the control group after immersion in heavy metals. Additionally, Cd 2+ and Pd 2+ in the food significantly influenced the mean lifespan of M. mongolica of the P and F 1 generations. Egg production per brood was also significantly impacted by Cd 2+ and Pb 2+ in the food in generation P. Interestingly, Pb 2+ was the only metal that significantly influenced the reproduction times of F 2 , while the reproductive times were significantly influenced by Cd 2+ for generation P. Moreover, Cd 2+ , Pb 2+ , and Hg 2+ in the food significantly influenced the fecundity of generation P. Evaluation of the population growth parameters of M. mongolica revealed that the intrinsic rate of increase, net reproduction rate, and finite rate of increase were significantly influenced by Cd 2+ , Pb 2+ , and Hg 2+ in the food in generation P. Additionally, Hg 2+ slightly impacted generation time for generation P. Finally, the acute toxicity toward M. mongolica was Hg 2+  > Cd 2+  > Pb 2+ . Overall, heavy metals in the food were likely to influence the growth, survival, and population growth of M. mongolica through the food chain.

Regional Variability of Cd, Hg, Pb and C Concentrations in Different Horizons of Swedish Forest Soils

International Nuclear Information System (INIS)

Alriksson, A.

2001-01-01

Contents of cadmium (Cd), mercury (Hg), lead (Pb) and carbon(C) in the O, B and C horizons of podzolized forest soils in Sweden were surveyed. Concentrations and storage of Cd, Hg and Pb in the O and B horizons were high in southern Sweden and gradually decreased towards the north, though with considerable local variability. This pattern reflects the influence of anthropogenic emissions of these metals, as well as the effects of soil-forming processes. Parent till material, as represented by the C horizon concentration of the respective metal, accounted for little of the variation in metal concentration in the O horizon. For Cd and Pb, the correlations were not significant or slightly negative (R 2 = 0.12 and 0.09 respectively) depending on region, while for Hg the correlation was not significant or slightly positive (R 2 = 0.03 and 0.08). Furthermore, parent till material accounted for more of the variation in metal concentrations in the B horizons in the northern part of Sweden than in the middle and southernmost parts, where the concentration of total carbon had more influence. The correlation between the metal concentrations in the B and C horizon was strongest for Pb (R 2 = 0.63 and 0.36 in the two northernmost regions), lower for Cd (R 2 = 0.19 and 0.16) and not significant for Hg. For all soil horizons, total C concentration accounted for much of the variation in Hg concentration in particular (O-horizon R 2 = 0.15-0.69, B horizon R 2 = 0.36-0.50, C horizon R 2 = 0.23-0.50 and ns in one region). Ratios of metal concentrations between the B and C horizons were highest for Hg(maximum value of 30), indicating a relatively larger addition or retention of Hg compared to Cd and Pb (maximum value of 10)in the B horizon. This study indicate that factors other than parent material account for the large scale variation in O horizon concentrations of metals but patterns correspond well with those of atmospheric deposition of heavy metals and acidifying substances

Sorption of Hg(II and Pb(II Ions on Chitosan-Iron(III from Aqueous Solutions: Single and Binary Systems

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Byron Lapo

2018-03-01

Full Text Available The present work describes the study of mercury Hg(II and lead Pb(II removal in single and binary component systems into easily prepared chitosan-iron(III bio-composite beads. Scanning electron microscopy and energy-dispersive X-ray (SEM-EDX analysis, Fourier transform infrared spectroscopy (FTIR, thermogravimetric analysis (TGA and point of zero charge (pHpzc analysis were carried out. The experimental set covered pH study, single and competitive equilibrium, kinetics, chloride and sulfate effects as well as sorption–desorption cycles. In single systems, the Langmuir nonlinear model fitted the experimental data better than the Freundlich and Sips equations. The sorbent material has more affinity to Hg(II rather than Pb(II ions, the maximum sorption capacities were 1.8 mmol·g−1 and 0.56 mmol·g−1 for Hg(II and Pb(II, respectively. The binary systems data were adjusted with competitive Langmuir isotherm model. The presence of sulfate ions in the multicomponent system [Hg(II-Pb(II] had a lesser impact on the sorption efficiency than did chloride ions, however, the presence of chloride ions improves the selectivity towards Hg(II ions. The bio-based material showed good recovery performance of metal ions along three sorption–desorption cycles.

Heavy metals (Pb, Cd, As and MeHg) as risk factors for cognitive dysfunction: A general review of metal mixture mechanism in brain.

Science.gov (United States)

Karri, Venkatanaidu; Schuhmacher, Marta; Kumar, Vikas

2016-12-01

Human exposure to toxic heavy metals is a global challenge. Concurrent exposure of heavy metals, such as lead (Pb), cadmium (Cd), arsenic (As) and methylmercury (MeHg) are particularly important due to their long lasting effects on the brain. The exact toxicological mechanisms invoked by exposure to mixtures of the metals Pb, Cd, As and MeHg are still unclear, however they share many common pathways for causing cognitive dysfunction. The combination of metals may produce additive/synergetic effects due to their common binding affinity with NMDA receptor (Pb, As, MeHg), Na + - K + ATP-ase pump (Cd, MeHg), biological Ca +2 (Pb, Cd, MeHg), Glu neurotransmitter (Pb, MeHg), which can lead to imbalance between the pro-oxidant elements (ROS) and the antioxidants (reducing elements). In this process, ROS dominates the antioxidants factors such as GPx, GS, GSH, MT-III, Catalase, SOD, BDNF, and CERB, and finally leads to cognitive dysfunction. The present review illustrates an account of the current knowledge about the individual metal induced cognitive dysfunction mechanisms and analyse common Mode of Actions (MOAs) of quaternary metal mixture (Pb, Cd, As, MeHg). This review aims to help advancement in mixture toxicology and development of next generation predictive model (such as PBPK/PD) combining both kinetic and dynamic interactions of metals. Copyright © 2016 Elsevier B.V. All rights reserved.

Relativistic pseudopotential model for superheavy elements: applications to chemistry of eka-Hg and eka-Pb

Energy Technology Data Exchange (ETDEWEB)

Zaitsevskii, Andrei V [Institute of Hydrogen Energetics and Plasma Technologies, Russian Research Centre ' Kurchatov Institute' (Russian Federation); Wuellen, C van [Technische Universitaet Kaiserslautern (Germany); Titov, A V [B P Konstantinov Petersburg Nuclear Physics Institute, Russian Academy of Sciences (Russian Federation)

2009-12-31

Relativistic pseudopotential approach to the electronic structure simulation of superheavy elements (SHE) compounds is presented. Advanced formulations of this approach leaving both valence and outer-core electronic shells for explicit treatment give rise to simple and efficient computational techniques ensuring highly accurate description of most chemical properties of SHE. At present, the errors due to the use of approximate methods for solving the correlation problem for a subsystem of valence electrons are much larger than those stemming from the pseudopotential approximation itself. Recent applications to the studies of the chemistry of elements 112 (eka-Hg) and 114 (eka-Pb) are reviewed; properties of these elements and their lighter homologues, Hg and Pb, are compared.

Theoretical study of heavy metal Cd, Cu, Hg, and Ni(II) adsorption on the kaolinite(0 0 1) surface

Energy Technology Data Exchange (ETDEWEB)

Zhao, Jian, E-mail: zhaojian0209@aliyun.com [Institute of Applied Physics and Computational Mathematics, PO Box 8009, Beijing 100088 (China); State Key Laboratory of Geomechanics and Deep Underground Engineering, China University of Mining and Technology, Beijing 100083 (China); He, Man-Chao [State Key Laboratory of Geomechanics and Deep Underground Engineering, China University of Mining and Technology, Beijing 100083 (China)

2014-10-30

Highlights: • We investigated the adsorption of Cd, Cu, Hg, and Ni(II) on kaolinite(0 0 1) surface. • The adsorption capabilities of the kaolinite for HM atoms were Ni > Cu > Cd > Hg(II). • The adsorption energy increases with the coverage for Cd, Cu, and Hg(II) atoms. • The adsorption energy decreases with the coverage for Ni(II) atoms. - Abstract: Heavy metal pollution is currently of great concern because it has been recognized as a potential threat to air, water, and soil. Adsorption was one of the most popular methods for the removal of heavy metal. The adsorption of heavy metal Cd, Cu, Hg, and Ni(II) atoms on the hydroxylated (0 0 1) surface of kaolinite was investigated using density-functional theory within the generalized gradient approximation and a supercell approach. The coverage dependence of the adsorption structures and energetics were systematically studied for a wide range of coverage Θ [from 0.11 to 1.0 monolayers (ML)] and adsorption sites. The most stable among all possible adsorption sites for Cd(II) atom was the two-fold bridge site followed by the one-fold top site, and the top site was the most favorite adsorption site for Cu and Ni(II) atoms, while the three-fold hollow site was the most stable adsorption site for Hg(II) atom followed by the two-fold bridge site. The adsorption energy increases with the coverage for Cd, Cu, and Hg(II) atoms, thus indicating the higher stability of surface adsorption and a tendency to the formation of adsorbate islands (clusters) with increasing the coverage. However, the adsorption energy of Ni(II) atoms decreases when increasing the coverage. The adsorption capabilities of the kaolinite clay for the heavy metal atoms were in the order of Ni > Cu > Cd > Hg(II). The other properties of the Cd, Cu, Hg, and Ni(II)/kaolinite(0 0 1) system including the different charge distribution, the lattice relaxation, and the electronic density of states were also studied and discussed in detail.

Theoretical study of heavy metal Cd, Cu, Hg, and Ni(II) adsorption on the kaolinite(0 0 1) surface

International Nuclear Information System (INIS)

Zhao, Jian; He, Man-Chao

2014-01-01

Highlights: • We investigated the adsorption of Cd, Cu, Hg, and Ni(II) on kaolinite(0 0 1) surface. • The adsorption capabilities of the kaolinite for HM atoms were Ni > Cu > Cd > Hg(II). • The adsorption energy increases with the coverage for Cd, Cu, and Hg(II) atoms. • The adsorption energy decreases with the coverage for Ni(II) atoms. - Abstract: Heavy metal pollution is currently of great concern because it has been recognized as a potential threat to air, water, and soil. Adsorption was one of the most popular methods for the removal of heavy metal. The adsorption of heavy metal Cd, Cu, Hg, and Ni(II) atoms on the hydroxylated (0 0 1) surface of kaolinite was investigated using density-functional theory within the generalized gradient approximation and a supercell approach. The coverage dependence of the adsorption structures and energetics were systematically studied for a wide range of coverage Θ [from 0.11 to 1.0 monolayers (ML)] and adsorption sites. The most stable among all possible adsorption sites for Cd(II) atom was the two-fold bridge site followed by the one-fold top site, and the top site was the most favorite adsorption site for Cu and Ni(II) atoms, while the three-fold hollow site was the most stable adsorption site for Hg(II) atom followed by the two-fold bridge site. The adsorption energy increases with the coverage for Cd, Cu, and Hg(II) atoms, thus indicating the higher stability of surface adsorption and a tendency to the formation of adsorbate islands (clusters) with increasing the coverage. However, the adsorption energy of Ni(II) atoms decreases when increasing the coverage. The adsorption capabilities of the kaolinite clay for the heavy metal atoms were in the order of Ni > Cu > Cd > Hg(II). The other properties of the Cd, Cu, Hg, and Ni(II)/kaolinite(0 0 1) system including the different charge distribution, the lattice relaxation, and the electronic density of states were also studied and discussed in detail

VALIDACIÓN DE LA METODOLOGÍA PARA LA DETERMINACIÓN DE SB, AS, CD, CU, CR, HG, NI, PB Y ZN EN SEDIMENTOS POR ICO-MS

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Hermógenes Rosas Rodríguez

2004-01-01

Full Text Available En este trabajo se presentan los resultados obtenidos en la validación de la técnica ICP-MS utilizada para la determinación de nueve elementos en sedimentos: Sb, As, Cd, Cu, Cr, Hg, Ni, Pb y Zn. Para ello se llevó a cabo el estudio de los siguientes parámetros de fiabilidad: precisión, exactitud y límites de detección y cuantificación. Para el análisis de estos elementos se utilizó un ICP-MS ELAN 6000 de Perkin Elmer®. El estudio de los distintos parámetros de validación fue muy satisfactorio para la mayoría de los analitos, alcanzándose límites de detección y de cuantificación muy bajos (inferiores a 1microg/l e incluso de 1 ng/l para el Cd. El método ICP-MS es exacto y preciso, obteniéndose para la mayoría de los elementos coeficientes de variación en torno al 2% y porcentajes de recuperación del 100%.

A macroalgae-based biotechnology for water remediation: Simultaneous removal of Cd, Pb and Hg by living Ulva lactuca.

Science.gov (United States)

Henriques, Bruno; Rocha, Luciana S; Lopes, Cláudia B; Figueira, Paula; Duarte, A C; Vale, Carlos; Pardal, M A; Pereira, E

2017-04-15

Metal uptake from contaminated waters by living Ulva lactuca was studied during 6 days, under different relevant contamination scenarios. In mono-metallic solutions, with concentrations ranging from 10 to 100 μg L -1 for Hg, 10-200 μg L -1 for Cd, and 50-1000 μg L -1 for Pb, macroalgae (500 mg L -1 , d.w.) were able to remove, in most cases 93-99% of metal, allowing to achieve water quality criteria regarding both surface and drinking waters. In multi-metallic solutions, comprising simultaneously the three metals, living macroalgae still performed well, with Hg removal (c.a. 99%) not being significantly affected by the presence of Cd and Pb, even when those metals were in higher concentrations. Removal efficiencies for Cd and Pb varied between 57 and 96%, and 34-97%, respectively, revealing an affinity of U. lactuca toward metals: Hg > Cd > Pb. Chemical quantification in macroalgae, after bioaccumulation assays demonstrated that all Cd and Hg removed from solution was really bound in macroalgae biomass, while only half of Pb showed to be sorbed on the biomass. Overall, U. lactuca accumulated up to 209 μg g -1 of Hg, up to 347 μg g -1 of Cd and up to 1641 μg g -1 of Pb, which correspond to bioconcentration factors ranging from 500 to 2200, in a dose-dependent accumulation. Pseudo-first order, pseudo-second order and Elovich models showed a good performance in describing the kinetics of bioaccumulation, in the whole period of time. In the range of experimental conditions used, no mortality was observed and U. lactuca relative growth rate was not significantly affected by the presence of metals. Results represent an important contribution for developing a macroalgae-based biotechnology, applied for contaminated saline water remediation, more "green" and cost-effective than conventional treatment methods. Copyright © 2017 Elsevier Ltd. All rights reserved.

Thermal oxidation of InP surfaces modified with NiO + PbO mixtures

International Nuclear Information System (INIS)

Mittova, I.Ya.; Tomina, E.V.; Samsonov, A.A.; Lukin, A.N.; Simonov, S.P.

2005-01-01

The oxidation kinetics of (NiO + PbO)/InP, NiO/InP and PbO/InP structures in an oxygen flow is studied in the temperature range of 400-550 deg C. It is shown by IR spectroscopy that the thermal oxidation of (NiO + PbO)/InP structures leads to the formation of nickel and lead polyphosphates and indium ortho- and metaphosphates. The nickel phosphates may then gradually transform into diphosphates, depending on the oxidation temperature, whereas the lead phosphates undergo no changes [ru

Electrothermal vaporization inductively coupled plasma-mass spectrometry for the determination of Cr, Cu, Cd, Hg and Pb in rice flour

International Nuclear Information System (INIS)

Li, P.-C.; Jiang, S.-J.

2003-01-01

Ultrasonic slurry sampling (USS)-electrothermal vaporization (ETV) dynamic reaction cell TM (DRC) inductively coupled plasma-mass spectrometry (ICP-MS) has been applied to determine Cr, Cu, Cd, Hg and Pb in rice samples. The influences of instrument operating conditions and slurry preparation on the ion signals were reported. Ascorbic acid was used as a modifier to enhance the ion signals. The background ions at the chromium masses were reduced in intensity significantly by using 0.4 ml min -1 NH 3 as reaction cell gas in the dynamic reaction cell while a q value of 0.6 was used. Since the sensitivities of Cr, Cu, Cd, Hg and Pb in rice flour slurry and aqueous solution were quite different, standard addition and isotope dilution methods were used for the determination of Cr, Cu, Cd, Hg and Pb in these rice samples. This method has been applied to the determination of Cr, Cu, Cd, Hg and Pb in NIST SRM 1568a rice flour reference material and two rice samples purchased from the market. The analytical results for the reference material agreed with the certified values. The results for the rice samples for which no reference values were available were also found to be in good agreement between the isotope dilution and standard addition methods. The method's detection limits estimated from the standard addition plots were about 0.44, 1.7, 0.4, 0.53 and 0.69 ng g -1 for Cr, Cu, Cd, Hg and Pb, respectively, in the original rice flour

Metal resistance mechanisms in Gram-negative bacteria and their potential to remove Hg in the presence of other metals.

Science.gov (United States)

Giovanella, Patricia; Cabral, Lucélia; Costa, Alexandre Pereira; de Oliveira Camargo, Flávio Anastácio; Gianello, Clesio; Bento, Fátima Menezes

2017-06-01

Contamination of the environment by heavy metals has been increasing in recent years due to industrial activities. Thus research involving microorganisms capable of surviving in multi-contaminated environments is extremely important. The objectives of the present study were to evaluate the removal of mercury alone and in the presence of cadmium, nickel and lead by four mercury-resistant microorganisms; estimate the removal of Cd, Ni and Pb; understand the mechanisms involved (reduction, siderophores, biofilms, biosorption and bioaccumulation) in the metal resistance of the isolate Pseudomonas sp. B50D; and determine the capacity of Pseudomonas sp. B50D in removing Hg, Cd, Ni and Pb from an industrial effluent. It was shown that the four isolates evaluated were capable of removing from 62% to 95% of mercury from a culture medium with no addition of other metals. The isolate Pseudomonas sp. B50D showed the best performance in the removal of mercury when evaluated concomitantly with other metals. This isolate was capable of removing 75% of Hg in the presence of Cd and 91% in the presence of Ni and Pb. With respect to the other metals it removed 60%, 15% and 85% of Cd, Ni and Pb, respectively. In tests with effluent, the isolate Pseudomonas sp. B50D removed 85% of Hg but did not remove the other metals. This isolate presented reduction, biosorption, biofilm production and siderophore production as its metal resistance mechanisms. Pseudomonas sp. B50D was thus a candidate with potential for application in the bioremediation of effluents with complex metal contaminations. Copyright © 2017 Elsevier Inc. All rights reserved.

Accurate calculation of superdeformed bands in Hg and Pb

International Nuclear Information System (INIS)

Lei Yian; Zeng Jinyan

1993-01-01

The superdeformed (SD) rotational bands in Hg and Pb are analyzed by means of the abc expression for rotational bands, which was derived from the Bohr Hamiltonian. The agreement between calculated and observed transition energies is incredibly well. The deviation of the calculated E' γ s from the observed results turns out to be absolute value δ ≤0.5 keV (except for a few cases, 0.5 kev ≤ absolute value δ ≤ 0.7 keV). Some transitions which have not been observed yet in these SD bands are also predicted, which may be useful for experimental investigation

Computer augumented modelling studies of Pb(II, Cd(II, Hg(II, Co(II, Ni(II, Cu(II and Zn(II complexes of L-glutamic acid in 1,2-propanediol–water mixtures

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MAHESWARA RAO VEGI

2008-12-01

Full Text Available Chemical speciation of Pb(II, Cd(II, Hg(II, Co(II, Ni(II, Cu(II and Zn(II complexes of L-glutamic acid was studied at 303 K in 0–60 vol. % 1,2-propanediol–water mixtures, whereby the ionic strength was maintained at 0.16 mol dm-3. The active forms of the ligand are LH3+, LH2 and LH–. The predominant detected species were ML, ML2, MLH, ML2H and ML2H2. The trend of the variation in the stability constants with changing dielectric constant of the medium is explained based on the cation stabilizing nature of the co-solvents, specific solvent–water interactions, charge dispersion and specific interactions of the co-solvent with the solute. The effect of systematic errors in the concentrations of the substances on the stability constants is in the order alkali > > acid > ligand > metal. The bioavailability and transportation of metals are explained based on distribution diagrams and stability constants.

Determination of Cd, Cr, Hg and Pb in plastics from waste electrical and electronic equipment by inductively coupled plasma mass spectrometry with collision-reaction interface technology.

Science.gov (United States)

Santos, Mirian C; Nóbrega, Joaquim A; Cadore, Solange

2011-06-15

A procedure based on the use of a quadrupole inductively coupled plasma-mass spectrometer equipped with a collision-reaction interface (CRI) for control of spectral overlap interferences was developed for simultaneous determination of Cd, Cr, Hg, and Pb in plastics from waste electrical and electronic equipment (WEEE). The injection of H(2) and He (80 and 60 mL min(-1), respectively) into the sampled plasma, colliding and reacting with potentially interfering polyatomic ions, allows interference-free determination of chromium via its isotopes (52)Cr and (53)Cr that are freed from overlap due to the occurrence of (40)Ar(12)C(+), (40)Ar(12)C(1)H(+), (36)S(16)O(+) or (1)H(36)S(16)O(+). Cadmium, Hg and Pb were directly determined via their isotopes (110)Cd, (111)Cd, (112)Cd, (199)Hg, (200)Hg, (201)Hg, (202)Hg, (206)Pb, (207)Pb, and (208)Pb, without using CRI. The CRI can be quickly activated or deactivated before each analyte measurement. Limits of detection for (52)Cr were 0.04 or 0.14 μg L(-1) with He or H(2) injected in CRI. Cadmium and Pb have LODs between 0.02 and 0.08 μg L(-1) and Hg had 0.93-0.98 μg L(-1), without using CRI. Analyte concentrations for samples varied from 16 to 43, 1 to 11, 4 to 12, and 5 to 13 mg kg(-1) for Cr, Cd, Hg and Pb, respectively. Copyright © 2011 Elsevier B.V. All rights reserved.

Certification of trace element contents (As, Cd, Co, Cu, Fe, Mn, Hg, Na, Pb and Zn) in a fly ash obtained from the combustion of pulverised coal

International Nuclear Information System (INIS)

Griepink, B.; Colinet, E.; Guzzi, G.; Haemers, L.; Muntau, H.

1983-01-01

The element contents of As, Cd, Co, Cu, Fe, Mn, Hg, Na, Pb and Zn of a fly ash from pulverised coal are certified. The procedures and their results for the homogenisation, the contamination and homogeneity checks and the analytical campaign are reported. The certified mass fractions and indicative values for Cr, Ni, Th, V and water soluble sulphate are given. The work was carried out within the framework of the activities of the Community Bureau of Reference (BCR) of the Commission of the European Communities. (orig.) [de

Binding Affinity of a Highly Sensitive Au/Ag/Au/Chitosan-Graphene Oxide Sensor Based on Direct Detection of Pb2+ and Hg2+ Ions

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Nur Hasiba Kamaruddin

2017-10-01

Full Text Available The study of binding affinity is essential in surface plasmon resonance (SPR sensing because it allows researchers to quantify the affinity between the analyte and immobilised ligands of an SPR sensor. In this study, we demonstrate the derivation of the binding affinity constant, K, for Pb2+ and Hg2+ ions according to their SPR response using a gold/silver/gold/chitosan–graphene oxide (Au/Ag/Au/CS–GO sensor for the concentration range of 0.1–5 ppm. The higher affinity of Pb2+ to binding with the CS–GO sensor explains the outstanding sensitivity of 2.05 °ppm−1 against 1.66 °ppm−1 of Hg2+. The maximum signal-to-noise ratio (SNR upon detection of Pb2+ is 1.53, and exceeds the suggested logical criterion of an SNR. The Au/Ag/Au/CS–GO SPR sensor also exhibits excellent repeatability in Pb2+ due to the strong bond between its functional groups and this cation. The adsorption data of Pb2+ and Hg2+ on the CS–GO sensor fits well with the Langmuir isotherm model where the affinity constant, K, of Pb2+ and Hg2+ ions is computed. The affinity of Pb2+ ions to the Au/Ag/Au/CS–GO sensor is significantly higher than that of Hg2+ based on the value of K, 7 × 105 M−1 and 4 × 105 M−1, respectively. The higher shift in SPR angles due to Pb2+ and Hg2+ compared to Cr3+, Cu2+ and Zn2+ ions also reveals the greater affinity of the CS–GO SPR sensor to them, thus supporting the rationale for obtaining K for these two heavy metals. This study provides a better understanding on the sensing performance of such sensors in detecting heavy metal ions.

Chemical Bath Deposition of PbS:Hg2+ Nanocrystalline Thin Films

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R. Palomino-Merino

2013-01-01

Full Text Available Nanocrystalline PbS thin films were prepared by Chemical Bath Deposition (CBD at 40 ± 2°C onto glass substrates and their structural and optical properties modified by in-situ doping with Hg. The morphological changes of the layers were analyzed using SEM and the X-rays spectra showing growth on the zinc blende (ZB face. The grain size determined by using X-rays spectra for undoped samples was found to be ~36 nm, whereas with the doped sample was 32–20 nm. Optical absorption spectra were used to calculate the Eg, showing a shift in the range 1.4–2.4 eV. Raman spectroscopy exhibited an absorption band ~135 cm−1 displaying only a PbS ZB structure.

Bioaccessibility of As, Cd, Cu, Ni, Pb, and Sb in toys and low-cost jewelry.

Science.gov (United States)

Guney, Mert; Zagury, Gerald J

2014-01-21

Children can be exposed to toxic elements in toys and jewelry following ingestion. As, Cd, Cu, Ni, Pb, and Sb bioavailability was assessed (n = 24) via the in vitro gastrointestinal protocol (IVG), the physiologically based extraction test (PBET), and the European Toy Safety Standard protocol (EN 71-3), and health risks were characterized. Cd, Cu, Ni, and Pb were mobilized from 19 metallic toys and jewelry (MJ) and one crayon set. Bioaccessible Cd, Ni, or Pb exceeded EU migratable concentration limits in four to six MJ, depending on the protocol. Using two-phase (gastric + intestinal) IVG or PBET might be preferable over EN 71-3 since they better represent gastrointestinal physiology. Bioaccessible and total metal concentrations were different and not always correlated, indicating that bioaccessibility measurement may provide more accurate risk characterization. More information on impacts of multiple factors affecting metals mobilization from toys and jewelry is needed before recommending specific tests. Hazard index (HI) for Cd, Ni, or Pb were >1 for all six MJ exceeding the EU limits. For infants (6-12 mo old), 10 MJ had HI > 1 for Cd, Cu, Ni, or Pb (up to 75 for Cd and 43 for Pb). Research on prolonged exposure to MJ and comprehensive risk characterization for toys and jewelry exposure is recommended.

Study of the nuclear reactions 208Pb + 58Ni and 208Pb + 64Ni with a focusing time-of-flight spectrometer

International Nuclear Information System (INIS)

Sapotta, K.

1983-01-01

In the first part of this thesis the construction of a time-of-flight spectrometer for heavy ions with magnetic focusing is described. Then ion trajectories are calculated, and the effective spatial angle and the angular resolution are determined. In the second part the study of quasielastic transfer and deep inelastic reactions of 58 Ni and 64 Ni with 208 Pb at E=265 MeV respectively 260 MeV by means of this spectrometer is described. (HSI) [de

Removal lead (Pb and mercury (Hg from juaro fish (Pangasius polyuranodon using citric acid from pineapple extract (Ananas comosus as chelating agent

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Pra Dian Mariadi

2017-10-01

Full Text Available An assessment of dietary risk of heavy metals exposure to human is important since it is the main of exposure. The aim of study to measure the contamination of lead and mercury in juaro fish meat and the effort to reduce contaminations using citric acid from pineapple extract as a chelating agent. Samples was soaked and boiled in citric acid extract at concentration 50%, 75 %, 100 % for, 15 min, 30 min, 45 min at 25 0C, 50 0C and 100 0C. The concentration of lead and mercury in Juaro fish lower than the maximum acceptable lever for Pb and Hg respectively (1mg/kg for Pb, 0,5 mg/Kg for Hg. The result indicated that after soaking and boiling in citric acid solution form pineapple extract at concentration 100 % for 45 min at 100 0C reducing heavy metals Pb from 0,02 mg.Kg-1 to 0,003 mg.Kg-1 and Hg from 0,011 mg.Kg-1 to lower than 0,0001 mg.Kg-1. The increasing of soaking time and boiling temperature, the levels of Pb and Hg in Juaro fish Tissue will decreasing.

Investigations of small-gap semiconductors: HgTe, HgMnTe and PbMnTe in the far infrared region using Fourierspectroscopic methods

International Nuclear Information System (INIS)

Roschger, I.

1985-05-01

A special method was developed in the framework of this thesis to solve the inherent problem of dynamic range in Fourier spectrometry by using optical compensation. The so-called dual beam spectrometer consists of two coupled interferometers. This technique was adapted for measurements on small gap semiconductors. The investigated sample was n-HgTe, for which a resonant acceptor absorption in the conduction band was predicted. By alloying Mn-ions into the inverted gap-HgTe-crystal the band gap can be tuned to an open gap band structure. The mixed crystal exhibits additional structures in the phonon spectrum. The model of Barker and Verleur (including clustering) was applied. The substitution of Mn-ions in the IV-VI-compound PbTe leads to semimagnetic effects resolved by magneto-reflectivity measurements. The extrapolation in the fan-charts to zero-magnetic field suggests residual spin splitting either in the conduction and/or in the valence band. To evaluate the data an oscillator fit was applied to cyclotron absorption (Faraday- and Voigt-configuration) and was proved to be in agreement with the experimental data. Zero field splitting appears in PbMnTe in the valence band and indicates a weak ferromagnetism already observed in other measurements cited in the literature. Kramers-Kronig-data were in agreement with the theoretical results of the Barker-Verleur-model. The influence of clustering in the mixed crystal HgMnTe on the phonon spectra must be taken into account for Mn concentrations > 20%. The existence of the resonance acceptor state in HgTe was proved by optical transmission measurements. (Author, shortened by G.Q.)

One century sedimentary record of Hg and Pb pollution in the Sagua estuary (Cuba) derived from 210Pb and 137Cs chronology

International Nuclear Information System (INIS)

Diaz-Asencio, M.; Alonso-Hernandez, C.M.; Bolanos-Alvarez, Y.; Gomez-Batista, M.; Pinto, V.; Morabito, R.; Hernandez-Albernas, J.I.; Eriksson, M.; Sanchez-Cabeza, J.A.

2009-01-01

The vertical distribution of Hg and Pb were determined in a sediment core collected from the Sagua estuary (North Cuba) that receives input from the Sagua river, one of the most polluted rivers discharging into the Cuban coastal environment. Depth profiles of metal concentrations were converted to time-based profiles using the 210 Pb dating method and confirmed with the 137 Cs fallout peak. The mean mass accumulation rate was estimated to be 0.17 ± 0.04 g cm -2 y -1 (mean sediment accumulation rate 0.52 ± 0.13 cm y -1 ) and the core bottom was estimated to date back about 130 years. The historical sedimentary record showed a strong enrichment of mercury concentrations in the past decades, caused by the incomplete treatment of industrial wastes from a chlor-alkali plant with mercury-cell technology in the Sagua river basin. Lead fluxes to sediments showed a gradual increase from the 1920s to present, which agrees with a population increase in Sagua la Grande City. Fluxes of both metals have increased the past 25 years, with values reaching a maximum of 0.5 and 3.9 μg cm -2 y -1 for Hg and Pb, respectively.

Highly selective and sensitive optical sensor for determination of Pb2+and Hg2+ ions based on the covalent immobilization of dithizone on agarose membrane

Science.gov (United States)

Zargoosh, Kiomars; Babadi, Fatemeh Farhadian

2015-02-01

A highly sensitive and selective optical membrane for determination of Hg2+ and Pb2+ was prepared by covalent immobilization of dithizone on agarose membrane. In addition to its high stability, reproducibility and relatively long lifetime, the proposed optical sensor revealed good selectivity for target ions over a large number of alkali, alkaline earth, transition, and heavy metal ions. The proposed optical membrane displays linear responses from 1.1 × 10-8 to 2.0 × 10-6 mol L-1 and 1.2 × 10-8 to 2.4 × 10-6 mol L-1 for Hg2+ and Pb2+, respectively. The limits of detection (LOD) were 2.0 × 10-9 mol L-1 and 4.0 × 10-9 mol L-1 for Hg2+ and Pb2, respectively. The prepared optical membrane was successfully applied to the determination of Hg2+ and Pb2+ in industrial wastes, spiked tap water and natural waters without any preconcentration step.

A Review on Heavy Metals (As, Pb, and Hg Uptake by Plants through Phytoremediation

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Bieby Voijant Tangahu

2011-01-01

Full Text Available Heavy metals are among the most important sorts of contaminant in the environment. Several methods already used to clean up the environment from these kinds of contaminants, but most of them are costly and difficult to get optimum results. Currently, phytoremediation is an effective and affordable technological solution used to extract or remove inactive metals and metal pollutants from contaminated soil and water. This technology is environmental friendly and potentially cost effective. This paper aims to compile some information about heavy metals of arsenic, lead, and mercury (As, Pb, and Hg sources, effects and their treatment. It also reviews deeply about phytoremediation technology, including the heavy metal uptake mechanisms and several research studies associated about the topics. Additionally, it describes several sources and the effects of As, Pb, and Hg on the environment, the advantages of this kind of technology for reducing them, and also heavy metal uptake mechanisms in phytoremediation technology as well as the factors affecting the uptake mechanisms. Some recommended plants which are commonly used in phytoremediation and their capability to reduce the contaminant are also reported.

Tolerance of Portulaca grandiflora to individual and combined application of Ni, Pb and Zn.

Science.gov (United States)

Mihailovic, N; Andrejić, G; Dželetović, Ž

2015-01-01

In the present study, metal accumulation capacity and tolerance of Portulaca grandiflora were investigated. Plants were grown under greenhouse conditions in pots on soil amended with Ni, Pb and Zn to the final concentration of 2 mmol kg(-1) for each metal. Results show considerable accumulating capacity and translocation of Ni and Zn, as well as significant accumulation of Pb in roots. A slight decrease of biomass with Zn and of chlorophyll content with Zn and Ni were observed, as well as an increase of proline content with each of the metals. Combinations of metals revealed mutual interference affecting both the uptake and translocation of the metals and their impact on physiological parameters. Results suggest that Portulaca grandiflora, although not a hyperaccumulator, shows a good tolerance and accumulation capacity for Ni, Pb and Zn, but, for the purposes of remediation, interference of the metals must be taken into account.

Highly enhanced photocurrent of novel quantum-dot-co-sensitized PbS-Hg/CdS/Cu:ZnO thin films for photoelectrochemical applications

International Nuclear Information System (INIS)

Gohel, Jignasa V.; Jana, A.K.; Singh, Mohit

2017-01-01

A novel quantum-dot-co-sensitized PbS-Hg/CdS/Cu:ZnO thin films synthesized by low-cost process. The properties of ZnO are also enhanced by doping and co-doping. It is also compared with quantum-dot co-sensitization. Optical properties, crystal structure, morphology, and photocurrent are characterized by UV-Vis spectroscopy, XRD, SEM, and solar simulator, respectively. The bandgap is interestingly reduced highly to 2.6 eV for Ag co-doped Cu:ZnO. It is unprecedentedly reduced to 2.1 eV and even 1.97 eV for CdS and PbS-Hg QD-sensitized thin films, respectively. An exceptionally enhanced photocurrent of 17.1 mA/cm"2 is achieved with PbS-Hg-co-sensitized CdS-sensitized Cu:ZnO thin film. This is an excellent achievement, which highly supports the potential of low-cost solar conversion. (orig.)

Highly enhanced photocurrent of novel quantum-dot-co-sensitized PbS-Hg/CdS/Cu:ZnO thin films for photoelectrochemical applications

Energy Technology Data Exchange (ETDEWEB)

Gohel, Jignasa V.; Jana, A.K.; Singh, Mohit [Sardar Vallabhbhai National Institute of Technology, Chemical Engineering Department, Surat, Gujarat (India)

2017-08-15

A novel quantum-dot-co-sensitized PbS-Hg/CdS/Cu:ZnO thin films synthesized by low-cost process. The properties of ZnO are also enhanced by doping and co-doping. It is also compared with quantum-dot co-sensitization. Optical properties, crystal structure, morphology, and photocurrent are characterized by UV-Vis spectroscopy, XRD, SEM, and solar simulator, respectively. The bandgap is interestingly reduced highly to 2.6 eV for Ag co-doped Cu:ZnO. It is unprecedentedly reduced to 2.1 eV and even 1.97 eV for CdS and PbS-Hg QD-sensitized thin films, respectively. An exceptionally enhanced photocurrent of 17.1 mA/cm{sup 2} is achieved with PbS-Hg-co-sensitized CdS-sensitized Cu:ZnO thin film. This is an excellent achievement, which highly supports the potential of low-cost solar conversion. (orig.)

History of atmospheric deposition of Cd, Hg, and Pb in North America: Evidence from lake and peat bog sediments

International Nuclear Information System (INIS)

Norton, S.A.; Dillon, P.J.; Evans, R.D.; Mierle, G.; Kahl, J.S.

1990-01-01

The precipitation chemistry and lake and peat sediment chemistry of three metals emitted to the atmosphere in significant amounts as a result of anthropogenic activity are reviewed. The three metals, Cd, Hg, and Pb, have contrasting source terms, atmospheric residence times, and chemical mobility. Lake and ombrotrophic peat bog sediments record increases in the concentrations and accumulation rates of the metals for most of temperate North America for the last 100 years. These increases are largely related to the burning of coal, smelting of nonferrous metals, the transportation industry, and the industrial production of chlorine. Modern atmospheric fluxes of Cd in central North America are about 1,000 times background fluxes; accumulation rates for Cd in sediments have increased two to 3 times above background, beginning about 100 years ago. Global scale Hg pollution off the atmosphere is suggested by concentrations in northern hemisphere air that are double the Hg content of southern hemisphere air. Accumulation rates of Hg in sediment have approximately doubled in the last 100 years. However, these rates are approximately an order of magnitude less than those for Cd. Modern increases in Pb concentrations are ubiquitous for all lakes examines thus far in North America. Input is from multiple sources and thus the timing of increased accumulation rates in sediment varies across the continent. Typical modern accumulation rates reach maxima at 20 to 30 mg/sq-m/yr, or 100 times that of Cd and 1,000 times that off Hg. Recent decreases in atmospheric lead are reflected in decreases in the accumulation rate of Pb in both lake and peat bog sediment in eastern North America

First-principles study for the enhanced sulfur tolerance of Ni(1 1 1) surface alloyed with Pb

Science.gov (United States)

Zhang, Yanxing; Yang, Zongxian

2018-04-01

The adsorption of H2S, HS, S, H and the dissociation of H2S on the Ni2Pb/Ni (1 1 1) are systematically studied using the first-principles method based on density functional theory. It is found that H2S dissociation barriers are greatly increased by alloying with Pb atoms in the Ni(1 1 1) surface, while the barrier for H2S formation is greatly reduced. In addition, the adsorption of sulfur atom is weakened a lot. The results indicate that alloying with Pb may be a good way to increase the sulfur tolerance of Ni based anode catalysts of solid oxide fuel cells.

Crystal growth and properties of PbI2 doped with Fe and Ni

International Nuclear Information System (INIS)

Rybak, O.V.; Lun', Yu.O.; Bordun, I.M.; Omelyan, M.F.

2005-01-01

A procedure is described for doping PbI 2 monocrystals with Fe and Ni during vapor-phase growth in a closed system in the presence of excess iodine. The rate of mass transfer in the system and the doping level of the crystals are shown to be governed by the dopant content in the source material and the source temperature. The effect of Fe and Ni doping on the low-temperature (5 K) exciton photoluminescence spectrum of PbI 2 is discussed [ru

Population health risk via dietary exposure to trace elements (Cu, Zn, Pb, Cd, Hg, and As) in Qiqihar, Northeastern China.

Science.gov (United States)

Luo, Jinming; Meng, Jia; Ye, Yajie; Wang, Yongjie; Bai, Lin

2018-02-01

The estimated daily intakes (EDIs) of six trace elements (Cu, Zn, Pb, Cd, Hg, and As) in vegetables (leafy vegetable, i.e., bok choy, fruit vegetables, i.e., cucumber and tomato, and other categories, i.e., mushroom, kidney bean, and potato), cereals (rice and wheat flour), and meats (pork, mutton, and beef) most commonly consumed by adult inhabitants of Qiqihar, Northeastern China, were determined to assess the health status of local people. The average EDIs of Cu, Zn, Pb, Cd, Hg, and As were with 20.77 μg (kg bw) -1 day -1 of Cu, 288 μg (kg bw) -1 day -1 of Zn, 2.01 μg (kg bw) -1 day -1 of Pb, 0.41 μg (kg bw) -1 day -1 of Cd, 0.01 μg (kg bw) -1 day -1 of Hg, and 0.52 μg (kg bw) -1 day -1 of As, respectively, which are below the daily allowance recommended by FAO/WHO. However, the maximum EDIs of Pb and Cd were 4.56 μg (kg bw) -1 day -1 and 1.68 μg (kg bw) -1 day -1 , respectively, which are above the recommended levels [i.e., 3.58 μg (kg bw) -1 day -1 for Pb and 1.0 μg (kg bw) -1 day -1 for Cd] by FAO/WHO. This finding indicates that the potential health risk induced by daily ingestion of Pb and Cd for the local residents should receive a significant concern. Similarly, we detected elevated Pb and Cd concentrations, i.e., with average of 13.58 and 0.60 mg kg -1 dw, respectively, in the adult scalp hairs. Consumption of rice, potato, bok choy, and wheat flour contributed to 75 and 82% of Pb and Cd daily intake from foodstuffs. Nevertheless, human scalp hair is inappropriate biological material for determination of the nutritional status of trace elements in this region.

Study on procedure for determination of Cr, As, Se, Cd, Hg, Pb in some kinds of herb products such as: kind of fungus, philamin... by ICP-MS

International Nuclear Information System (INIS)

Pham Ngoc Khai; Do Van Thuan; Nguyen Thi Kim Dung; Nguyen Hong Minh

2007-01-01

The determination of Cr, As, Se, Cd, Hg, Pb in herb products such as: kind of fungus, philamin, etc by ICP-MS has been studied. The effects of the parameters of ICP-MS instrument, concentration of nitric acid and high concentration of some elements on the determination of Cr, As, Se, Cd, Hg, Pb by ICP-MS has been concerned. The study and choice the suitable internal standard for the accurate determination of Hg has been sold. The suitable parameters of the microwave, composition and content of the acid mixture for the complete decomposition of the sample have been studied. The recommended procedure has been applied to the determination of Cr, As, Se, Cd, Hg, Pb in the standard samples and real samples. The error of the results is acceptable. (author)

Behaviors of heavy metals (Cd, Cu, Ni, Pb and Zn) in soil amended with composts.

Science.gov (United States)

Gusiatin, Zygmunt Mariusz; Kulikowska, Dorota

2016-09-01

This study investigated how amendment with sewage sludge compost of different maturation times (3, 6, 12 months) affected metal (Cd, Cu, Ni, Pb, Zn) bioavailability, fractionation and redistribution in highly contaminated sandy clay soil. Metal transformations during long-term soil stabilization (35 months) were determined. In the contaminated soil, Cd, Ni and Zn were predominately in the exchangeable and reducible fractions, Pb in the reducible fraction and Cu in the reducible, exchangeable and oxidizable fractions. All composts decreased the bioavailability of Cd, Ni and Zn for up to 24 months, which indicates that cyclic amendment with compost is necessary. The bioavailability of Pb and Cu was not affected by compost amendment. Based on the reduced partition index (IR), metal stability in amended soil after 35 months of stabilization was in the following order: Cu > Ni = Pb > Zn > Cd. All composts were more effective in decreasing Cd, Ni and Zn bioavailability than in redistributing the metals, and increasing Cu redistribution more than that of Pb. Thus, sewage sludge compost of as little as 3 months maturation can be used for cyclic amendment of multi-metal-contaminated soil.

Perovskite LaPbMSbO6 (M=Co, Ni): Structural distortion, magnetic and dielectric properties

International Nuclear Information System (INIS)

Bai, Yijia; Han, Lin; Liu, Xiaojuan; Deng, Xiaolong; Wu, Xiaojie; Yao, Chuangang; Liang, Qingshuang; Meng, Junling; Meng, Jian

2014-01-01

The B-site ordered double perovskite oxides LaPbMSbO 6 (M=Co, Ni) have been synthesized via the modified Sol–Gel precursor two-step route. Rietveld refinements reveal strong abnormal structural distortion and BO 6 octahedral deformation appearing along the ab plane. Owing to the cooperative Jahn–Teller effect of Co 2+ and Pb 2+ ions, the Co-related compound exhibits almost complete Co 2+ –Sb 5+ order. For magnetic properties, spin-canted antiferromagnetic state with high extent of magnetic frustration is confirmed. The Ni-related compound presents heavier magnetic frustration for introducing tiny disorder on site occupation accompanied with valence state and further enhancing the complexity of magnetic competition. Dielectric measurements present a considerable temperature dependent dielectric relaxation with great dc-like loss feature in the LaPbCoSbO 6 . For LaPbNiSbO 6 , however, the permittivity with low dielectric loss is shown to be insensitive to either temperature or frequency. The corresponding electronic active energy manifests that the weakly bounded 3d-electron is prone to hop in a more distorted Co–Sb sublattice. - Graphical abstract: XRD Rietveld refinement result of LaPbCoSbO 6 presented a large BO 6 octahedral distortion along the ab plane. Based upon the variations from Co–O–Sb bond angles, a fierce competition from many extended magnetic coupling routes (M–O–O–M) would induce a considerably large magnetic frustration and electron hopping restriction. - Highlights: • Highly ordered LaPbMSbO 6 (M=Co, Ni) were synthesized. • Abnormal structural distortion appeared in the ab plane. • Strong magnetic frustration was confirmed via M 2+ –O–O–M 2+ route. • Dielectric measurements presented a large difference between Co and Ni samples. • 3d-electronic structure determines lattice distortion and physical properties

Anthropogenic contributions to atmospheric Hg, Pb and As accumulation recorded by peat cores from southern Greenland and Denmark dated using the 14C "bomb pulse curve"

Science.gov (United States)

Shotyk, W.; Goodsite, M. E.; Roos-Barraclough, F.; Frei, R.; Heinemeier, J.; Asmund, G.; Lohse, C.; Hansen, T. S.

2003-11-01

Mercury concentrations are clearly elevated in the surface and sub-surface layers of peat cores collected from a minerotrophic ("groundwater-fed") fen in southern Greenland (GL) and an ombrotrophic ("rainwater-fed") bog in Denmark (DK). Using 14C to precisely date samples since ca. AD 1950 using the "atmospheric bomb pulse," the chronology of Hg accumulation in GL is remarkably similar to the bog in DK where Hg was supplied only by atmospheric deposition: this suggests not only that Hg has been supplied to the surface layers of the minerotrophic core (GL) primarily by atmospheric inputs, but also that the peat cores have preserved a consistent record of the changing rates of atmospheric Hg accumulation. The lowest Hg fluxes in the GL core (0.3 to 0.5 μg/m 2/yr) were found in peats dating from AD 550 to AD 975, compared to the maximum of 164 μg/m 2/yr in AD 1953. Atmospheric Hg accumulation rates have since declined, with the value for 1995 (14 μg/m 2/yr) comparable to the value for 1995 obtained by published studies of atmospheric transport modelling (12 μg/m 2/yr). The greatest rates of atmospheric Hg accumulation in the DK core are also found in the sample dating from AD 1953 and are comparable in magnitude (184 μg/m 2/yr) to the GL core; again, the fluxes have since gone into strong decline. The accumulation rates recorded by the peat core for AD 1994 (14 μg/m 2/yr) are also comparable to the value for 1995 obtained by atmospheric transport modelling (18 μg/m 2/yr). Comparing the Pb/Ti and As/Ti ratios of the DK samples with the corresponding crustal ratios (or "natural background values" for preanthropogenic peat) shows that the samples dating from 1953 also contain the maximum concentration of "excess" Pb and As. The synchroneity of the enrichments of all three elements (Hg, Pb, and As) suggests a common source, with coal-burning the most likely candidate. Independent support for this interpretation was obtained from the Pb isotope data ( 206Pb/ 207Pb

Iminodiacetic acid functionalized polypyrrole modified electrode as Pb(II) sensor: Synthesis and DPASV studies

International Nuclear Information System (INIS)

Joseph, Alex; Subramanian, Sankaran; Ramamurthy, Praveen C.; Sampath, Srinivasan; Kumar, R. Vasant; Schwandt, Carsten

2014-01-01

Graphical abstract: - Abstract: An electrochemical lead ion sensor has been developed by modification of carbon paste electrode (CPE) using polypyrrole functionalized with iminodiacetic acid (IDA-PPy) containing carboxyl group. The electrochemical response of Pb 2+ ion on the IDA-PPy modified CPE has been evaluated and the controling parameters have been optimized using differential pulse anodic stripping voltammetry (DPASV). The IDA-PPy modified CPE shows a linear correlation for Pb 2+ concentrations in the range of 1 × 10 −6 to 5 × 10 −9 M and the lower detection limit of Pb 2+ has been found to be 9.6 × 10 −9 M concentration. Other tested metal ions, namely Cu 2+ , Cd 2+ , Co 2+ , Hg 2+ , Ni 2+ and Zn 2+ , do not exhibit any voltammetric stripping response below 1 × 10 −7 M concentration. However, the Pb 2+ response is affected in the presence of molar equivalents or higher concentrations of Cu 2+ , Cd 2+ and Co 2+ ions in binary systems with Pb 2+ , consequent to their ability to bind with iminodiacetic acid, while Hg 2+ , Ni 2+ and Zn 2+ do not interfere at all. A good correlation has been observed between the lead concentrations as analyzed by DPASV using IDA-PPy modified CPE and atomic absorption spectrophotometry for a lead containing industrial effluent sample

KONTAMINASI LOGAM BERAT MERKURI (Hg DAN TIMBAL (Pb PADA AIR, SEDIMEN DAN IKAN SELAR TETENGKEK (Megalaspis cordyla L DI TELUK PALU, SULAWESI TENGAH

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Matius Paundanan

2015-09-01

Full Text Available Palu bay waters is susceptible to heavy metal pollution due to the inclusion of the waste product of Palu city, and such as agriculture, and traditional mining. The objective of this research was to determine the contamination of heavy metals mercury (Hg and lead (Pb in water, sediment, and torpedo scad fish (Megalaspis cordyla. Sampling was done purposively at 10 sampling points. Parameters of water quality measurements were done in the field for temperature, pH, brightness, turbidity, and dissolved oxygen (DO, and at laboratory analysis for salinity, chemical oxygen demand (COD, ammonia, and nitrates. Heavy metals were analized by following APHA, and Indonesian National Standard (SNI methods. The results showed that Hg consentrations in water, sediment, gill, meat, liver, and spleen were 0.0008-0.0042 mg/l, 0.017-0.287 mg/kg, 0.007-0.145 mg/kg, 0.014-0.046 mg/kg, 0.052-0.106 mg/kg, and 0.043-0.414 mg/kg, respectively. Pb concentrations in water, sediments, gill, meat, liver, and spleen were 0.0130-0.0392 mg/l, 2.647-8.987 mg/kg, 0.132-0.775 mg/kg, 0.005-0.734 mg/kg, 0.295-1.871 mg/kg, and 1.654-12.92 mg/kg, respectively. The average of Hg and Pb concentrations in the water had exceeded the specified quality standards, while in the sediment were still below the quality standards. The average of Hg and Pb concentrations in all observed fish organs were below the quality standards, except for Pb concentrations in gill, liver, and spleen.Keywords: heavy metals, water, sediment, Megalaspis cordyla, Palu Bay

FTIR spectroscopic study on the Hofmann -Td- type clathrates: Ni(benzoic acid)2M(CN)4.aniline (M=Zn, Cd, Hg)

International Nuclear Information System (INIS)

Kesan, G.; Kartal, Z.

2010-01-01

The Hofmann-Td-type clathrates formulated as Ni(L) 2 M(CN) 4 .nG where L is a bidentate or a pair of unidentate ligand molecule, M is Zn, Cd or Hg, G is a guest molecule and n is the number of guest molecule. The host lattice of the Hofmann-Td-type clathrates is formed from endless chains of -Ni-L-L-Ni-L-L-Ni- and M(CN) 4 ions arranged between the consecutive crossing -Ni-L-L-Ni-L-L-Ni- chains with the O-ends bound to the Ni metal atoms. These polymeric layers are held in parallel by Van der Walls interaction between ligand molecules. This structure provides α-type cavity. In this study, Ni(Benzoic Acid ) 2M(CN) 4 .Aniline (M = Zn, Cd, Hg) is obtained for the first time by means of chemical methods in powder form and their infrared spectra are reported in range of (4000-400) cm - 1. The spectral data suggest that the new clathrates are similar in structure to the Hofmann-type clathrates.

Potential of sunflower (helianthus annuus L.) for phytoremediation of nickle (Ni) and lead (Pb) contaminated water

International Nuclear Information System (INIS)

Mukhtar, S.M.; HAQ Bhatti, H.N.; Khalid, M.; Haq, M.A; Shahzad, S.M.

2010-01-01

Heavy metals are contaminants of much environmental apprehension, as they are hazardous to human being and other biota. Buildup of heavy metals in crop plants is of great concern due to the probability of food contamination through the soil-root interface. For this purpose, a hydroponic study was conducted to evaluate the efficacy of sunflower plant to phytoremediate Pb and Ni contaminated water in the absence and presence of synthetic chelator. Results showed that application of Ni and Pb reduced the dry weights of shoot and root (up to 55.1 and 38.3%; 50.5 and 33.6%), shoot and root length (up to 64.5 and 58.1%; 64.1 and 55.8%), chlorophyll content (up to 63.8 and 54.4%), and photosynthetic activity (up to 66.1 and 62.7%), respectively with EDTA as compared to control. While, maximum concentration of Ni and Pb in shoot and root (up to 18.43 and 20.73 mg kg/sup -1/; 12.82 and 18.67 mg kg/sup -1/), total accumulation (up to 55.82 and 72.28 mg kg/sup -1/), and proline content (up to 128.2 and 98.3%) were recorded in the presence of EDTA respectively as compared to control. Generally, it was observed that concentration and total accumulation of Pb was more than Ni in sunflower plant. The study concludes that the use of synthetic chelator increased the uptake and translocation of heavy metals in plant biomass that could enhance the phytoremediation of Ni and Pb from contaminated water. (author)

The determination of the surface potential for the CdxHg1-xTe crystals and the V-CdxHg1-xTe and Ni-V-CdxMg1-xTe structures

International Nuclear Information System (INIS)

Veliyulin, Eh.I.; Ragimova, R.A.; Mamedov, A.A.

1996-01-01

Surface potential of semiconductor crystals n-Cd x Hg 1-x Te (unannealed and annealed in mercury vapors) and of the structures V-Cd x Hg 1-x Te, Ni-V-Cd x Hg 1-x Te has been defined using spectroscopy of weak-field electric reflection. It is shown that a deep penetration of vanadium atoms in near the surface region of the crystal occurs in the structures on the basis of unannealed Cd x Hg 1-x Te. 1 ref.; 4 figs

An experimental and thermodynamic equilibrium investigation of the Pb, Zn, Cr, Cu, Mn and Ni partitioning during sewage sludge incineration.

Science.gov (United States)

Liu, Jingyong; Fu, Jiewen; Ning, Xun'an; Sun, Shuiyu; Wang, Yujie; Xie, Wuming; Huang, Shaosong; Zhong, Sheng

2015-09-01

The effects of different chlorides and operational conditions on the distribution and speciation of six heavy metals (Pb, Zn, Cr, Cu, Mn and Ni) during sludge incineration were investigated using a simulated laboratory tubular-furnace reactor. A thermodynamic equilibrium investigation using the FactSage software was performed to compare the experimental results. The results indicate that the volatility of the target metals was enhanced as the chlorine concentration increased. Inorganic-Cl influenced the volatilization of heavy metals in the order of Pb>Zn>Cr>Cu>Mn>Ni. However, the effects of organic-Cl on the volatility of Mn, Pb and Cu were greater than the effects on Zn, Cr and Ni. With increasing combustion temperature, the presence of organic-Cl (PVC) and inorganic-Cl (NaCl) improved the transfer of Pb and Zn from bottom ash to fly ash or fuse gas. However, the presence of chloride had no obvious influence on Mn, Cu and Ni. Increased retention time could increase the volatilization rate of heavy metals; however, this effect was insignificant. During the incineration process, Pb readily formed PbSiO4 and remained in the bottom ash. Different Pb compounds, primarily the volatile PbCl2, were found in the gas phase after the addition of NaCl; the dominant Pb compounds in the gas phase after the addition of PVC were PbCl2, Pb(ClO4)2 and PbCl2O4. Copyright © 2015. Published by Elsevier B.V.

Chemically modified activated carbon with 1-acylthiosemicarbazide for selective solid-phase extraction and preconcentration of trace Cu(II), Hg(II) and Pb(II) from water samples.

Science.gov (United States)

Gao, Ru; Hu, Zheng; Chang, Xijun; He, Qun; Zhang, Lijun; Tu, Zhifeng; Shi, Jianping

2009-12-15

A new sorbent 1-acylthiosemicarbazide-modified activated carbon (AC-ATSC) was prepared as a solid-phase extractant and applied for removing of trace Cu(II), Hg(II) and Pb(II) prior to their determination by inductively coupled plasma optical emission spectrometry (ICP-OES). The separation/preconcentration conditions of analytes were investigated, including effects of pH, the shaking time, the sample flow rate and volume, the elution condition and the interfering ions. At pH 3, the maximum static adsorption capacity of Cu(II), Hg(II) and Pb(II) onto the AC-ATSC were 78.20, 67.80 and 48.56 mg g(-1), respectively. The adsorbed metal ions were quantitatively eluted by 3.0 mL of 2% CS(NH2)2 and 2.0 mol L(-1) HCl solution. Common coexisting ions did not interfere with the separation. According to the definition of IUPAC, the detection limits (3sigma) of this method for Cu(II), Hg(II) and Pb(II) were 0.20, 0.12 and 0.45 ng mL(-1), respectively. The relative standard deviation under optimum conditions is less than 4.0% (n=8). The prepared sorbent was applied for the preconcentration of trace Cu(II), Hg(II) and Pb(II) in certified and water samples with satisfactory results.

Oblate L = 1 bands in 194,196-201Pb, and 193Hg

International Nuclear Information System (INIS)

Becker, J.A.; Kuhnert, A.; Stoyer, M.A.; Brinkman, M.J.; Wang, T.F.; Roy, N.; Cizewski, J.A.; Stephens, F.S.; Deleplanque, M.A.; Diamond, R.M.; Azaiez, F.; Macchiavelli, A.O.; Korten, W.; Draper, J.E.; California Univ., Berkeley, CA

1992-11-01

Reports of recent experiments have included observations of regular and irregular bands in neutron deficient Pb isotopes with A=194, 196--201. The bands are populated strongly in HI,xn reactions. The shared characteristics of the bands include: (1) Bandhead energies of few MeV; (2) High bandhead spin; (3) Large alignments; (4) Small dynamic moments of inertia, and (5) Strong L = 1 transitions and weaker L = 2 crossover transitions, with B(Ml/B(E2)) ∼ 20 μ 2 /e 2 b 2 . Lifetimes of band members in the 198 Pb regular band are B(Ml) ∼ 1 W.u., and B(E2) ∼ 10 W.u. (with large errors). These observations are consistent with an interpretation of the regular structures as collective oblate bands with both proton and neutron excitations involved; the closed proton shell at Z = 82 is broken, and coupled to v(i l3/2 ) -n excitations. The irregular structures may correspond to triaxial shapes, with similar orbits involved. A similar structure has been also found in 193 Hg

Assessment of Pb, Zn, Cu, Ni and Cr in vegetables grown around Zanjan

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A. Afshari

2017-05-01

Full Text Available This study was conducted aimed to assess the potential risk of heavy metals on human health resulting from consumption of vegetables. To this end, the vegetables grown around town and industrial center of Zanjan were sampled randomly. Plant samples were digested using hydrochloric acid (HCL 2 M and concentration of elements (Pb, Zn, Cu, Ni and Cr were recorded by atomic absorption. Obtained means of heavy metals in all vegetables (N= 32 for Zn, Pb, Cu, Ni and Cr is 98.8, 31.9, 19.3, 4.4 and 2.3 mg/kg, respectively. The highest amount of metal pollution index (MPI in the basil and the lowest was observed in the garden cress (respectively 16.46 and 4.88. Daily intake (EDI for zinc, copper and chromium in all age groups was lower than the provisional tolerable daily intake (PTDI. This amount for nickel was 2, 1.6 and 1.3 %, and for Pb 28.1, 22 and 19 % higher than PTDI in children, adults and seniors, respectively. The potential risk (THQ was calculated in all age groups as Pb>>Cu>Zn>Ni>Cr. The potential risks (THQ of chromium, nickel and zinc were calculated lower than 1, for copper a bit more of 1 and for lead much higher than 1. Health index (HI for children, adults and the elderly was estimated 31.331, 24.58 and 21.14, respectively, with the largest contribution of the lead (89.7%.

Adsorption-desorption characteristics of Ni, Zn and Pb in soils of a landfill environment in Metro Manila, Philippines

International Nuclear Information System (INIS)

Castañeda, Soledad S.; Cuarto, Christina D.; David, Carlos Primo C.

2015-01-01

This study investigated the sorption-desorption characteristics of Ni, Zn, and Pb on two soil types in the environment of a municipal waste disposal facility. Batch experiments were carried out in ambient temperature and in unadjusted and close to soil field pH conditions. The kinetics of of adsorption fitted a pseudo second-order model. Rate constants were calculated and an empirical model for predicting adsorption of metal ions at a given time was derived from these constants. The equilibrium sorption capacities for the heavy metals in the clay and sandy loam soils were estimated using the Linear, Freundlich, and Langmuir isotherm models. The sorption process of Ni, Pb, and Zn in both soils generally fitted well with the Freundlich isotherm model at moderate to high initial concentration range of the metals. The Langmuir isotherm was applicable to the adsorption of Ni and Zn only. The adsorption capacity of the clay soil for the metals followed the order Zn > Pb > Ni. In the sandy loam soil, the adsorption capacity for the metals under the same conditions followed the order Pb > Zn > Ni. The adsorption capacities for the metals were in order of 1mg/g in both the landfill clay soil and the Lukutan River sandy loam soil, with slightly higher values for the clay soil. Desorption was minimal, less than 1% in the clay soil and about 2% in the sandy loam soil. Sorption reversibility tests showed that the retention of the metals in both soils follows the order Ni> Pb> Zn. (author)

Assessment of Cr, Ni and Pb Pollution in Rural Agricultural Soils of Tonalite-Trondjhemite Series in Central India.

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Shukla, Kriti; Kumar, Bijendra; Agrawal, Rahul; Priyanka, Kumari; Venkatesh, Madavi; Anshumali

2017-06-01

Chromium (Cr), nickel (Ni) and lead (Pb) contamination was investigated in wheat cultivated rain-fed and irrigated rural agricultural soils (n = 31) of Tonalite-Trondjhemite Series in Central India. The soil sampling was carried out by using stratified random sampling method. The mean concentrations of Cr, Ni and Pb were 54.8, 38.1 and 68.9 mg/kg, respectively. The average values of enrichment factor (EF), geoaccumulation index (I geo ) and contamination factor (CF) followed the order as: Pb > Ni > Cr. Distribution patterns of soil parent material and weathering processes govern mineral enrichments, irrespective of rainfed or irrigated agricultural practices. Principal component analysis (PCA) showed strong loading of Cr and Ni (PC1) and Pb and clay (PC3). The strong loading on Cr and Ni indicates soils are originating from basic and volcanic rocks in the study area. The strong loading of Pb and clay indicates Pb is strongly adsorbed on clay minerals and Fe-oxides. The cancer risk (CR) index showed negligible carcinogenic risk to the residing population. However, hazard index (HI) values for children exceed the safe limit (HI > 1) for Cr and Pb. Spatial distribution of pollution load index suggest highest pollution in the northeastern part of the district. The study revealed that geogenically enriched soils of the area are suitable for agricultural activities under present conditions.

The use of Pb, Sr, and Hg isotopes in Great Lakes precipitation as a tool for pollution source attribution

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The anthropogenic emission and subsequent deposition of heavy metals including mercury (Hg) and lead (Pb) presents human health and environmental concerns. Although it is known that local and regional sources of these metals contribute to deposition in the Great Lakes region, it ...

Perovskite LaPbMSbO{sub 6} (M=Co, Ni): Structural distortion, magnetic and dielectric properties

Energy Technology Data Exchange (ETDEWEB)

Bai, Yijia [State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, 5625 Renmin Street, Changchun 130022 (China); Chemical Engineering College, Inner Mongolia University of Technology, 49 Aimin Street, Hohhot 010051 (China); Han, Lin [State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, 5625 Renmin Street, Changchun 130022 (China); University of Chinese Academy of Sciences, Beijing 10049 (China); Liu, Xiaojuan, E-mail: lxjuan@ciac.jl.cn [State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, 5625 Renmin Street, Changchun 130022 (China); Deng, Xiaolong [State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, 5625 Renmin Street, Changchun 130022 (China); University of Chinese Academy of Sciences, Beijing 10049 (China); Wu, Xiaojie [State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, 5625 Renmin Street, Changchun 130022 (China); Yao, Chuangang; Liang, Qingshuang; Meng, Junling [State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, 5625 Renmin Street, Changchun 130022 (China); University of Chinese Academy of Sciences, Beijing 10049 (China); Meng, Jian, E-mail: jmeng@ciac.jl.cn [State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, 5625 Renmin Street, Changchun 130022 (China)

2014-09-15

The B-site ordered double perovskite oxides LaPbMSbO{sub 6} (M=Co, Ni) have been synthesized via the modified Sol–Gel precursor two-step route. Rietveld refinements reveal strong abnormal structural distortion and BO{sub 6} octahedral deformation appearing along the ab plane. Owing to the cooperative Jahn–Teller effect of Co{sup 2+} and Pb{sup 2+} ions, the Co-related compound exhibits almost complete Co{sup 2+}–Sb{sup 5+} order. For magnetic properties, spin-canted antiferromagnetic state with high extent of magnetic frustration is confirmed. The Ni-related compound presents heavier magnetic frustration for introducing tiny disorder on site occupation accompanied with valence state and further enhancing the complexity of magnetic competition. Dielectric measurements present a considerable temperature dependent dielectric relaxation with great dc-like loss feature in the LaPbCoSbO{sub 6}. For LaPbNiSbO{sub 6}, however, the permittivity with low dielectric loss is shown to be insensitive to either temperature or frequency. The corresponding electronic active energy manifests that the weakly bounded 3d-electron is prone to hop in a more distorted Co–Sb sublattice. - Graphical abstract: XRD Rietveld refinement result of LaPbCoSbO{sub 6} presented a large BO{sub 6} octahedral distortion along the ab plane. Based upon the variations from Co–O–Sb bond angles, a fierce competition from many extended magnetic coupling routes (M–O–O–M) would induce a considerably large magnetic frustration and electron hopping restriction. - Highlights: • Highly ordered LaPbMSbO{sub 6} (M=Co, Ni) were synthesized. • Abnormal structural distortion appeared in the ab plane. • Strong magnetic frustration was confirmed via M{sup 2+}–O–O–M{sup 2+} route. • Dielectric measurements presented a large difference between Co and Ni samples. • 3d-electronic structure determines lattice distortion and physical properties.

Assessment of Phytoextraction Potential of Fenugreek (Trigonellafoenum-graecum L. to Remove Heavy Metals (Pb and Ni from Contaminated Soil

Directory of Open Access Journals (Sweden)

Leela Kaur

2015-02-01

Full Text Available The objective of the present study was to evaluate the effect of metal mobilizing agents, ethelynediaminetetraacetic acid (EDTA and salicylic acid (SA, on the accumulation and translocation of lead (Pb and nickel (Ni by fenugreek (Trigonellafoenum-graecumL. plants in contaminated soil. EDTA and SA were amended at 100 mM and 1.0 mM respectively. Pb and Ni content were estimated using ICP-OES. Plant samples were prepared for scanning electron microscope (SEM analysis to investigate metals distribution in different tissues (root, stem and leaf of plant. The results showed that EDTA increased Pb and Ni uptake as compared to SA. SEM analysis revealed that in the presence of EDTA, the deposition of Pb particles was predominantly in vascular tissues of the stem and leaf.    

Removal of Ni (II), Co (II) and Pb (II) ions from aqueous media using ...

African Journals Online (AJOL)

Removal of Ni (II), Co (II) and Pb (II) ions from aqueous media using Starch ... The results showed that 0.025 % loaded SSMNPs gave the optimal sorption ... constants (Lagergren and Pseudo-2nd-order) for Ni2+ and Co2+ adsorption were ... Langmuir correlation coefficients showed a better fit for the adsorption isotherms.

[Heavy metals contents and Hg adsorption characteristics of mosses in virgin forest of Gongga Mountain].

Science.gov (United States)

Liang, Peng; Yang, Yong-Kui; He, Lei; Wang, Ding-Yong

2008-06-01

Seven main moss species in the Hailuogou virgin forest of Gongga Mountain were sampled to determine their heavy metals (Hg, Cr, Cd, Ni, Pb, Cu, Mn, Zn and Fe) content, and two widely distributed species, Pleurozium schreberi (Brid.) Mitt. and Racomitrium laetum Besch., were selected to study their Hg adsorption characteristics. The results showed that the heavy metals contents in the mosses were lower than the background values in Europe and America, except that the Cd had a comparable value, which indicated that the atmosphere in study area was not polluted by heavy metals and good in quality. The Hg adsorption by P. schreberi and R. laetum was an initiative and rapid process, with the equilibrium reached in about two hours, and could be well fitted by Freundlich and Langmuir equations. Based on Langmuir equation, the maximum Hg adsorption capacities of P. schreberi and R. laetum were 15.24 and 8.19 mg x g(-1), respectively, suggesting that the two mosses had a good capacity of Hg adsorption, and could be used as the bio-monitors of atmospheric Hg pollution.

Adsorption Kinetics and intra particulate diffusivities of Hg, As and Pb ions on unmodified and thiolated coconut fiber

International Nuclear Information System (INIS)

Igwe, J. C.; Abia, A. A.; Ibeh, C. A.

2008-01-01

As, Hg and Pb are examples of heavy metals which are present in different types of industrial effluents responsible for environmental pollution. Their removal is traditionally made by chemical precipitation, ion-exchange and so on. However, this is expensive and not completely feasible to reduce their concentrations to the levels as low as required by the environmental legislation. Bio sorption is a process in which solids of natural origin are employed for binding the heavy metal. It is a promising alternative method to treat industrial effluents, mainly because of its low cost and high metal binding capacity. The kinetics was studied for bio sorption experiments using coconut fiber for As (III), Hg (II) and Pb (II) ions adsorption. The specific surface area and surface charge density of the coconut fiber are 1.186x10 25 (m 2 /g) and 5.39 xI0 24 (meq/m 2 ), respectively. The maximum adsorption capacity was found to be the highest for Pb (II) followed by Hg (II) and As (Ill). The modification of the adsorbent by thiolation affected the adsorption capacity. Equilibrium sorption was reached for the metal ions at about 60 min. The equilibrium constant and free energy of the adsorption at 30 degree were calculated. The mechanism of sorption was found to obey the particle-diffusion model. The kinetic studies showed that the sorption rates could be described by both pseudo first-order and pseudo second-order models. The pseudo second-order model showed a better fit with a rate constant value of 1.16x10 -4 /min. for all three metal ions.Therefore, the results of this study show that coconut fiber, both modified and unmodified, is an efficient adsorbent for the removal of toxic and valuable metals from industrial effluents

Hybrid porous phosphate heterostructures as adsorbents of Hg(II) and Ni(II) from industrial sewage

International Nuclear Information System (INIS)

Jimenez-Jimenez, J.; Algarra, M.; Rodriguez-Castellon, E.; Jimenez-Lopez, A.; Esteves da Silva, J.C.G.

2011-01-01

Porous phosphate heterostructures (PPH), functionalized with different ratios of aminopropyl and mercaptopropyl groups, labelled as N x=5,25,50 -PPH and S x=5,25,50 -PPH, respectively, were tested as adsorbents for Ni(II) and Hg(II) found in industrial sewage from electroplating processes and button battery recycling. X-ray diffraction was used to study the structures. The specific surface area of the pristine material (PPH) was 620 m 2 g -1 , whereas the specific surface areas of the modified mercaptopropyl (S 5 -PPH) and aminopropyl (N 5 -PPH) were 472 and 223 m 2 g -1 , respectively. The adsorption data were fitted to a Langmuir isotherm model. The S 5 -PPH material was saturated by 120 mmol Hg(II) per 100 g of material, whereas for Ni(II) adsorption, N 25 -PPH material displayed the highest adsorption with a saturation value of 43.5 mmol per 100 g. These results suggest that functionalized PPH materials may be promising toxic metal scavengers and that they may provide an alternative environmental technology.

Hybrid porous phosphate heterostructures as adsorbents of Hg(II) and Ni(II) from industrial sewage

Energy Technology Data Exchange (ETDEWEB)

Jimenez-Jimenez, J., E-mail: jjimenez@uma.es [Departamento de Quimica Inorganica, Facultad de Ciencias, Universidad de Malaga, Campus de Teatinos s/n, 29071 Malaga (Spain); Algarra, M. [Centro de Geologia do Porto, Faculdade de Ciencias, Universidade do Porto. Rua do, Campo Alegre 687, 4169-007 Porto (Portugal); Rodriguez-Castellon, E.; Jimenez-Lopez, A. [Departamento de Quimica Inorganica, Facultad de Ciencias, Universidad de Malaga, Campus de Teatinos s/n, 29071 Malaga (Spain); Esteves da Silva, J.C.G. [Centro de Investigacao em Quimica (CIQ-UP), Faculdade de, Ciencias da Universidade do Porto, Rua do Campo Alegre 687, 4169-007 Porto (Portugal)

2011-06-15

Porous phosphate heterostructures (PPH), functionalized with different ratios of aminopropyl and mercaptopropyl groups, labelled as N{sub x=5,25,50}-PPH and S{sub x=5,25,50}-PPH, respectively, were tested as adsorbents for Ni(II) and Hg(II) found in industrial sewage from electroplating processes and button battery recycling. X-ray diffraction was used to study the structures. The specific surface area of the pristine material (PPH) was 620 m{sup 2} g{sup -1}, whereas the specific surface areas of the modified mercaptopropyl (S{sub 5}-PPH) and aminopropyl (N{sub 5}-PPH) were 472 and 223 m{sup 2} g{sup -1}, respectively. The adsorption data were fitted to a Langmuir isotherm model. The S{sub 5}-PPH material was saturated by 120 mmol Hg(II) per 100 g of material, whereas for Ni(II) adsorption, N{sub 25}-PPH material displayed the highest adsorption with a saturation value of 43.5 mmol per 100 g. These results suggest that functionalized PPH materials may be promising toxic metal scavengers and that they may provide an alternative environmental technology.

Assessment of Ni, Cu, Zn and Pb levels in beach and dune sands from Havana resorts, Cuba.

Science.gov (United States)

Díaz Rizo, Oscar; Buzón González, Fran; Arado López, Juana O

2015-11-15

Concentrations of nickel (Ni), copper (Cu), zinc (Zn) and lead (Pb) in beach and dune sands from thirteen Havana (Cuba) resorts were estimated by X-ray fluorescence analysis. Determined mean metal contents (in mg·kg(-1)) in beach sand samples were 28±12 for Ni, 35±12 for Cu, 31±11 for Zn and 6.0±1.8 for Pb, while for dune sands were 30±15, 38±22, 37±15 and 6.8±2.9, respectively. Metal-to-iron normalization shows moderately severe and severe enrichment by Cu. The comparison with sediment quality guidelines shows that dune sands from various resorts must be considered as heavily polluted by Cu and Ni. Almost in every resort, the Ni and Cu contents exceed their corresponding TEL values and, in some resorts, the Ni PEL value. The comparison with a Havana topsoil study indicates the possible Ni and Cu natural origin. Copyright © 2015 Elsevier Ltd. All rights reserved.

Electronic environments in Ni{sub 3}Pb{sub 2}S{sub 2} (shandite) and its initial oxidation in air

Energy Technology Data Exchange (ETDEWEB)

Skinner, William M.; Qian, Gujie [Ian Wark Research Institute, ARC Special Research Centre for Particle and Material Interfaces, University of South Australia, Mawson Lakes, SA 5095 (Australia); Buckley, Alan N., E-mail: a.buckley@unsw.edu.au [School of Chemistry, University of New South Wales, Sydney, NSW 2052 (Australia)

2013-10-15

Polycrystalline Ni{sub 3}Pb{sub 2}S{sub 2} (shandite) was synthesised as a non-porous ingot to enable representative surfaces prepared by fracture under UHV to be characterised by X-ray photoelectron spectroscopy (XPS) before and after exposure to air. For an unoxidised surface, the S 2p{sub 3/2} binding energy was found to be significantly lower than those reported previously for shandite itself and other sulfides having shandite structure, and consistent with the physical and chemical properties of the shandites. The core electron binding energies for the three constituent elements were in agreement with the formal oxidation state representation Ni{sup 0}{sub 3}Pb{sup II}{sub 2}S{sup −II}{sub 2}, analogous to that deduced previously for Ni{sub 3}Sn{sub 2}S{sub 2}. Shandite surfaces were found to oxidise rapidly when initially exposed to air under ambient conditions, and concomitant with the formation of the Ni–O and Pb–O species, to restructure to NiS- and PbS-like surface phases having S core electron binding energies no higher than those for shandite. - Graphical abstract: Shandite ingot fracture surface in sample holder. Display Omitted - Highlights: • Shandite synthesised as ingot so that fracture surfaces were representative of bulk. • Surfaces prepared by fracture in vacuum characterised by XPS. • S 2p{sub 3/2} binding energy in range expected and lower than reported previously. • Ni, Pb and S core electron binding energies consistent with Ni{sup 0}{sub 3}Pb{sup II}{sub 2}S{sup −II}{sub 2}.

Study of the analytic quality in the determinations of Cr, Fe, Mn, Cu, Zn, Pb and Hg through conventional and nuclear analytical techniques in mosses of the MATV; Estudio de la calidad analitica en las determinaciones de Cr, Fe, Mn, Cu, Zn, Pb y Hg a traves de tecnicas analiticas nucleares y convencionales en musgos de la ZMVT

Energy Technology Data Exchange (ETDEWEB)

Caballero S, B.

2013-07-01

To evaluate the environmental risks of air pollution and to facilitate the decision-making for control, is necessary to have the capacity to generate data with analytical quality. A comparison between nuclear (Neutron activation analysis and total reflection X-ray fluorescence spectrometry) and no nuclear analytical techniques (atomic absorption spectrometry and inductively coupled plasma optical emission spectrometry) for simultaneous determination of metal content (Cr, Cu, Fe, Hg, Mn, Pb and Zn) in mosses from Metropolitan Area of the Toluca Valley (MATV) was performed. Epiphytic mosses (Fabriona ciliaris and Leskea angustata) were sampled in two campaigns, 16 sites (urban, transition and natural) and were prepared for each technique. The biological certified reference materials were used for the quality control and to evaluate accuracy, precision, linearity, detection and quantification limits. Results show that nuclear analytical techniques and no nuclear applied in chemical analysis of Cr, Cu, Fe, Hg, Mn, Pb and Zn in moss from MATV are comparable and therefore all of these can potentially be used for this purpose. However, if its considered both, the performance parameters and economic/operational characteristics is widely recommended inductively coupled plasma optical emission spectrometry, conventional analytical technique, which showed the highest analytical grade quality. Also were observed spatial and temporal variations in the concentrations of Cr, Cu, Fe, Hg, Mn, Pb and Zn in mosses from MATV and was discussed its potential origin. The urban sites had the highest concentration of anthropogenic elements as Cr, Cu, Fe, Hg, Pb and Zn because are strongly impacted by roads with high vehicle traffic. (Author)

Levels determination of heavy elements (Fe, Cu, Zn, Pb and Hg) in sword fish caught from the bay of Ghazaouet

International Nuclear Information System (INIS)

Chalabi, A.; Malek, M.; Ghomari, M.; Benamar, M.A.; Tchantchane, A.; Azbouche, A.; Toumert, I.; Benouali, N.; Tobbeche, S. , Algiers; Algeria)

1993-04-01

The nuclear technics 'PIXE' and 'XRF', were used for heavy metals analysis (Fe, Cu, Zn, Pb, and Hg), in sword fish (xiphias Gladius) caught in Ghazaouet bay. Muscles, liver and gonads were analysed. The methods gave similar results. A bioaccumulation phenomenon was observed except for Hg. The high amount of concentrations found liver, especially in the case of confirms that liver is a storage organ. The high levels of Zn seem to be due to the industrial wastes from the electrolyte plant in the region. All values were lower than the admissible norms

Biosynthesis of micro- and nanocrystals of Pb (II), Hg (II) and Cd (II) sulfides in four Candida species: a comparative study of in vivo and in vitro approaches.

Science.gov (United States)

Cuéllar-Cruz, Mayra; Lucio-Hernández, Daniela; Martínez-Ángeles, Isabel; Demitri, Nicola; Polentarutti, Maurizio; Rosales-Hoz, María J; Moreno, Abel

2017-03-01

Nature produces biominerals (biogenic minerals) that are synthesized as complex structures, in terms of their physicochemical properties. These biominerals are composed of minerals and biological macromolecules. They are produced by living organisms and are usually formed through a combination of chemical, biochemical and biophysical processes. Microorganisms like Candida in the presence of heavy metals can biomineralize those metals to form microcrystals (MCs) and nanocrystals (NCs). In this work, MCs and NCs of PbS, HgS or HgCl 2 as well as CdS are synthesized both in vitro (gels) and in vivo by four Candida species. Our in vivo results show that, in the presence of Pb 2+ , Candida cells are able to replicate and form extracellular PbS MCs, whereas in the presence of Hg 2+ and Cd 2+ , they did synthesize intercellular MCs from HgS or HgCl 2 and CdS NCs respectively. The MCs and NCs biologically obtained in Candida were compared with those PbS, HgS and CdS crystals synthetically obtained in vitro through the gel method (grown either in agarose or in sodium metasilicate hydrogels). This is, to our knowledge, the first time that the biosynthesis of the various MCs and NCs (presented in several species of Candida) has been reported. This biosynthesis is differentially regulated in each of these pathogens, which allows them to adapt and survive in different physiological and environmental habitats. © 2017 The Authors. Microbial Biotechnology published by John Wiley & Sons Ltd and Society for Applied Microbiology.

Soil heavy metal pollution and risk assessment associated with the Zn-Pb mining region in Yunnan, Southwest China.

Science.gov (United States)

Cheng, Xianfeng; Danek, Tomas; Drozdova, Jarmila; Huang, Qianrui; Qi, Wufu; Zou, Liling; Yang, Shuran; Zhao, Xinliang; Xiang, Yungang

2018-03-07

The environmental assessment and identification of sources of heavy metals in Zn-Pb ore deposits are important steps for the effective prevention of subsequent contamination and for the development of corrective measures. The concentrations of eight heavy metals (As, Cd, Cr, Cu, Hg, Ni, Pb, and Zn) in soils from 40 sampling points around the Jinding Zn-Pb mine in Yunnan, China, were analyzed. An environmental quality assessment of the obtained data was performed using five different contamination and pollution indexes. Statistical analyses were performed to identify the relations among the heavy metals and the pH in soils and possible sources of pollution. The concentrations of As, Cd, Pb, and Zn were extremely high, and 23, 95, 25, and 35% of the samples, respectively, exceeded the heavy metal limits set in the Chinese Environmental Quality Standard for Soils (GB15618-1995, grade III). According to the contamination and pollution indexes, environmental risks in the area are high or extremely high. The highest risk is represented by Cd contamination, the median concentration of which exceeds the GB15618-1995 limit. Based on the combination of statistical analyses and geostatistical mapping, we identified three groups of heavy metals that originate from different sources. The main sources of As, Cd, Pb, Zn, and Cu are mining activities, airborne particulates from smelters, and the weathering of tailings. The main sources of Hg are dust fallout and gaseous emissions from smelters and tailing dams. Cr and Ni originate from lithogenic sources.

Excellent corrosion resistance of 18Cr-20Ni-5Si steel in liquid Pb-Bi

International Nuclear Information System (INIS)

Kurata, Y.; Futakawa, M.

2004-01-01

The corrosion properties of three austenitic steels with different Si contents were studied under oxygen-saturated liquid Pb-Bi condition for 3000 h. The three austenitic steels did not exhibit appreciable dissolution of Ni and Cr at 450 deg. C. At 550 deg. C, the thick ferrite layer produced by dissolution of Ni and Cr was found in JPCA and 316SS with low Si contents while the protective oxide film composed of Si and O was formed on 18Cr-20Ni-5Si steel and prevented dissolution of Ni and Cr

Investigation of Gamma and Neutron Shielding Parameters for Borate Glasses Containing NiO and PbO

OpenAIRE

Singh, Vishwanath P.; Badiger, N. M.

2014-01-01

The mass attenuation coefficients, μ/ρ, half-value layer, HVL, tenth-value layer, TVL, effective atomic numbers, ZPIeff, and effective electron densities, Ne,eff, of borate glass sample systems of (100-x-y) Na2B4O7 : xPbO : yNiO (where x and y=0, 2, 4, 6, 8, and 10 weight percentage) containing PbO and NiO, with potential gamma ray and neutron shielding applications, have been investigated. The gamma ray interaction parameters, μ/ρ, HVL, TVL, ZPIeff, and Ne,eff, were computed for photon energ...

Study of heavy metal concentration (As, Ba, Cd, Hg, Pb, Crin water resources and river of Borujerd city in 2008-2009

Directory of Open Access Journals (Sweden)

bahram kamarehei

2010-02-01

Full Text Available with industrial and economic growth and different material production that humans gained from natural resources for their comfort and walfare, inwardly introduced toxic material and heavy metal entered environment that there created serious problems for themselves and environment. This study accomplished to determine heavy metal concentration (As, Ba, Cd, Hg, Pb, Crin water resources and river of Borujerd city in 2008-2009. Materials and Methods: This descriptive cross-sectional study was conducted to determine heavy metal concentration (As, Ba, Cd, Hg, Pb, Cr in water resources and river of Borujerd city. 54 samples of water were taken from 18 drinking water wells, and also in two times 8 samples of Borujerd river were taken from before and after the city. Then samples carried into the lab and were concentrated ten times using expressed methods and standard methods. Then heavy metal concentration determined by AAP (WFX 130 and results analyzed by SPSS and EXCEL software. Results: Heavy metal concentration average (As, Ba, Cd, Hg, Pb, Cr in drinking water wells were 0. 0, 0. 3222, 0. 0014, 0. 0002, 0. 0077 mg/l respectively. and heavy metal concentration in river water after the city has been increased than before the city. Conclusion: Results indicated that heavy metal concentration average in Borujerd drinking water wells were lower than standard amounts and drinking water wells didn’t pollute with heavy metal. But heavy metal concentration in river water after the city has been increased than the before of it because city waste water enters the city river.

Simultaneous trace-levels determination of Hg(II) and Pb(II) ions in various samples using a modified carbon paste electrode based on multi-walled carbon nanotubes and a new synthesized Schiff base

International Nuclear Information System (INIS)

Afkhami, Abbas; Bagheri, Hasan; Khoshsafar, Hosein; Saber-Tehrani, Mohammad; Tabatabaee, Masoumeh; Shirzadmehr, Ali

2012-01-01

Highlights: ► A new chemically modified carbon paste electrode was constructed and used. ► A new Schiff base and multi-walled carbon nanotube was used as a modifier. ► The electrochemical properties of the modified electrode were studied. ► The electrode was used to the simultaneous determination of Pb 2+ and Hg 2+ . - Abstract: A modified carbon paste electrode based on multi-walled carbon nanotubes (MWCNTs) and 3-(4-methoxybenzylideneamino)-2-thioxothiazolodin-4-one as a new synthesized Schiff base was constructed for the simultaneous determination of trace amounts of Hg(II) and Pb(II) by square wave anodic stripping voltammetry. The modified electrode showed an excellent selectivity and stability for Hg(II) and Pb(II) determinations and for accelerated electron transfer between the electrode and the analytes. The electrochemical properties and applications of the modified electrode were studied. Operational parameters such as pH, deposition potential and deposition time were optimized for the purpose of determination of traces of metal ions at pH 3.0. Under optimal conditions the limits of detection, based on three times the background noise, were 9.0 × 10 −4 and 6.0 × 10 −4 μmol L −1 for Hg(II) and Pb(II) with a 90 s preconcentration, respectively. In addition, the modified electrode displayed a good reproducibility and selectivity, making it suitable for the simultaneous determination of Hg(II) and Pb(II) in real samples such as sea water, waste water, tobacco, marine and human teeth samples.

Optimization of simultaneous electrochemical determination of Cd(II), Pb(II), Cu(II) and Hg(II) at carbon nanotube-modified graphite electrodes.

Science.gov (United States)

Pikna, L'ubomír; Heželová, Mária; Kováčová, Zuzana

2015-01-01

The health of the environment is worsening every day. Monitoring of potentially toxic elements and remediation of environmental pollution are necessary. Therefore, the research and development of simple, inexpensive, portable and effective sensors is important. Electrochemistry is a useful component of the field of environment monitoring. The present study focuses on evaluating and comparing three types of electrodes (PIGE, PIGE/MWCNT/HNO3 and PIGE/MWCNT/EDTA/HNO3) employed for the simultaneous electrochemical determination of four potentially toxic elements: Cd(II), Pb(II), Cu(II) and Hg(II). Cyclic voltammograms were measured in an acetate buffer. The LOD, LOQ, the standard and relative precisions of the method and a prediction intervals were calculated (according to the technical procedure DIN 32 645) for the three electrodes and for each measured element. The LOD for PIGE/CNT/HNO3 (the electrode with narrowest calculated prediction intervals) was 2.98 × 10(-7) mol L(-1) for Cd(II), 4.83 × 10(-7) mol L(-1) for Pb(II), 3.81 × 10(-7) mol L(-1) for Cu(II), 6.79 × 10(-7) mol L(-1) for Hg(II). One of the benefits of this study was the determination of the amount of Hg(II) in the mixture of other elements.

Highly Sensitive and Selective In-Situ SERS Detection of Pb(2+), Hg(2+), and Cd(2+) Using Nanoporous Membrane Functionalized with CNTs.

Science.gov (United States)

Shaban, Mohamed; Galaly, A R

2016-05-04

Porous Anodic Alumina (PAA) membrane was functionalized with CoFe2O4 nanoparticles and used as a substrate for the growing of very long helical-structured Carbon Nanotubes (CNTs) with a diameter less than 20 nm. The structures and morphologies of the fabricated nanostructures were characterized by field emission- scanning electron microscopy (FE-SEM), energy dispersive X-ray (EDX), and Raman spectroscopy. By uploading the CNTs on PAA, the characteristic Raman peaks of CNTs and PAA showed 4 and 3 times enhancement, respectively, which leads to more sensitive Surface-Enhanced Raman Spectroscopy (SERS) substrates. For comparison, PAA and CNTs/PAA arrays were used as SERS substrates for the detection of Hg(2+), Cd(2+), and Pb(2+). The proposed sensor demonstrated high sensitivity and selectivity between these heavy metal ions. CNTs/PAA sensor showed excellent selectivity toward Pb(2+) over other metal ions, where the enhancement factor is decreased from ~17 for Pb(2+) to ~12 for Hg(2+) and to ~4 for Cd(2+). Therefore, the proposed CNTs/PAA sensor can be used as a powerful tool for the determination of heavy metal ions in aqueous solutions.

Highly Sensitive and Selective In-Situ SERS Detection of Pb2+, Hg2+, and Cd2+ Using Nanoporous Membrane Functionalized with CNTs

Science.gov (United States)

Shaban, Mohamed; Galaly, A. R.

2016-01-01

Porous Anodic Alumina (PAA) membrane was functionalized with CoFe2O4 nanoparticles and used as a substrate for the growing of very long helical-structured Carbon Nanotubes (CNTs) with a diameter less than 20 nm. The structures and morphologies of the fabricated nanostructures were characterized by field emission- scanning electron microscopy (FE-SEM), energy dispersive X-ray (EDX), and Raman spectroscopy. By uploading the CNTs on PAA, the characteristic Raman peaks of CNTs and PAA showed 4 and 3 times enhancement, respectively, which leads to more sensitive Surface-Enhanced Raman Spectroscopy (SERS) substrates. For comparison, PAA and CNTs/PAA arrays were used as SERS substrates for the detection of Hg2+, Cd2+, and Pb2+. The proposed sensor demonstrated high sensitivity and selectivity between these heavy metal ions. CNTs/PAA sensor showed excellent selectivity toward Pb2+ over other metal ions, where the enhancement factor is decreased from ~17 for Pb2+ to ~12 for Hg2+ and to ~4 for Cd2+. Therefore, the proposed CNTs/PAA sensor can be used as a powerful tool for the determination of heavy metal ions in aqueous solutions. PMID:27143512

Bonding and Moessbauer Isomer Shifts in （Hg,Pb）—1223 Cuprate

Institute of Scientific and Technical Information of China (English)

高发明; 田永君; 谌岩; 李东春; 董海峰; 张思远

2003-01-01

By using the chemical bond theory of dielectric description,the chemical bond parameters of(Hg,Pb)-1223 were calculated.The results show that the(Ba,Sr)-O and Ca-0 types of bond have higher ionic character,while the Cu-O and(Hg,Pb)-0 types of bond have more covalent character.Moessbauer isomer shifts of 57Fe and 119Sn doped in(Hg,Pb)-1223 were calculated by using the chemical environmental factor,he,defined by covalency and electronic polarizability.Four valence state tin and three valence iron sites were identified in 57Fe and 119Sn doped(Hg,Pb)-1223 superconductor.It can be concluded that all of the Fe atoms substitute the Cu at square planar Cu(1) site,Whereas Sn prefers to substitute the square pyramidal Cu(2) site.

Pb and Hg heavy metal tolerance of single- and mixedspecies biofilm (Rhodotorula mucilaginosa and Escherichia coli

Directory of Open Access Journals (Sweden)

Buzejić Anica

2016-01-01

Full Text Available The aim of this study was to examine heavy metal tolerance (lead (Pb2+ and mercury (Hg2+ of single- and mixed-species biofilms, formed by yeast Rhodotorula mucilaginosa and bacteria Escherichia coli LM1. Single- and mixed-species biofilms were quantified by crystal violet test and the absorbance was measured using microplate reader (OD570. The minimal inhibitory concentration (MIC and the minimal lethal concentration (MLC were determined and the results were confirmed by fluorescence microscopy. The significant difference in lead tolerance was observed between the mixed- and the single-species biofilms. The MIC of lead (Pb2+ for the examined biofilms (E. coli LM1, R. mucilaginosa and R. mucilaginosa / E. coli was recorded at concentrations of 4000 μg/ml, 4000 μg/ml and 16000 μg/ml, respectively. The MIC of mercury (Hg2+ for the biofilms was noticed at concentrations of 31.25 μg/ml, 250 μg/ml and 250 μg/ml, respectively. Standard antibiotics (amphotericin B and tetracycline were used as positive control. Results obtained for single-species biofilms were compared in between and with the results obtained for mixed-species biofilm. The tolerance of the mixed- species biofilm was higher in comparison to the singlespecies biofilms and the results were confirmed by a fluoresecence microscope. The obtained results suggest that the R. mucilaginosa / E. coli biofilm may have a potential to be used in bioremediation of wastewaters contaminated with lead and mercury.

Metallothionein-Like Proteins and Energy Reserve Levels after Ni and Pb Exposure in the Pacific White Prawn Penaeus vannamei

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Gabriel Nunez-Nogueira

2010-01-01

Full Text Available This study analyzed the changes in metallothionein-like proteins (MTLPs and Energy Reserves (ERs in hepatopancreas and abdominal muscle of the white prawn Penaeus vannamei. Realistic metal concentration exposure for 10 days to Ni and Pb in solution revealed that juvenile prawns partially induce MTLP in hepatopancreas after Pb exposure. Ni was distributed equally between soluble and insoluble fractions, while Pb was present only in the insoluble fraction, suggesting different detoxification strategy. No changes in lipids and glycogen concentration were detected under these experimental conditions in both tissues analyzed. MTLP could not be considered as a suitable indicator for lead exposure in hepatopancreas.

Evaluation of potential of adsorption of U, Th, Pb, Zn and Ni by coconut fibers; Avaliacao do potencial de adsorcao de U, Th, Pb, Zn e Ni pelas fibras de coco

Energy Technology Data Exchange (ETDEWEB)

Monteiro, Raquel Almeida

2009-07-01

The residual biomass from agricultural activities has been evaluated as biosorbent for metals and organic composts from aqueous solutions, because of its adsorptive properties, low cost, abundance and to be a renewable resource. In this work, the efficiency of coir pith as biosorbent for the removal of U, Th, Pb, Zn e Ni ions from the aqueous solutions is presented. The coir pith is a by-product of the harvest of the coconut, a renewable natural source. The study was conducted by batch method. The influence of pH from 1 to 8, the dosage of the coir pith and the equilibrium time were studied. The adsorption of metal ions increased with the increase of pH and the dose. The Langmuir and Freundlich models were applied to describe the adsorption equilibrium isotherm. The kinetic process was studied using the pseudo-first order and pseudo-second order models. The Gibbs free energy was calculated. In the concentration range of 100 mg.L{sup -1} - 500 mg.L{sup -1}, the adsorption process was described better by the Langmuir equation for Pb{sup 2+} and Zn{sup 2+} ions and the Freundlich equation for UO{sub 2} 2{sup +}, Th{sup 4+} and Ni{sup 2+} ions, and represented by the pseudo-second order model. The biosorption process for removal of metal ions from the solutions was considered spontaneous. The results were promising, showing perspectives of application of coir pith as biosorbent of U, Th, Pb, Zn and Ni ions in wastewater treatment processes. (author)

Evaluation of vermicompost as bioadsorbent substrate of Pb, Ni, V and Cr for waste waters remediation using Total Reflection X-ray Fluorescence

International Nuclear Information System (INIS)

Urdaneta, Cynthia; Parra, Lue-Meru Marco; Matute, Saida; Garaboto, Mayantino Angel; Barros, Hayden; Vazquez, Cristina

2008-01-01

The use of vermicompost as adsorbent substrate for removing Pb, Ni, V and Cr from waste waters is proposed. In this work, after a preliminary physical and chemical characterization of the vermicompost, the optimal parameters for the heavy metal adsorption were obtained. A synthetic multielemental solution of Pb, Cr and Ni and a solution of NH 4 VO 3 for vanadium were evaluated. The optimized parameters were pH, vermicompost mass to volume ratio, agitation time and particle size of the adsorbent. A batch system was employed for the assays. The elements were determined in the supernatant solution after filtration of the substrate. An optimal pH of 4.5 was found for ion removal. The agitation time slightly influences the adsorption of Pb and Cr, but it has a high influence on the Ni and V adsorption. The highest adsorption and removal of the metals was observed for a vermicompost mass of 2 g per 500 mL using a particle size between 75 to 841 μm for Pb, Cr and Ni, and 841 till 1192 μm for V. The mean removal percentage for each element is around 95% for Pb. Ni and Cr in the multielemental synthetic sample, demonstrating a high removal capacity of the substrate. For V it was found a removal efficiency of 50%

Dielectric enhancement of PbZr{sub 0.3}Ti{sub 0.7}O{sub 3}/LaNiO{sub 3} multilayer thick film

Energy Technology Data Exchange (ETDEWEB)

Fan, Yasong; Chen, Xiaoyang; Habibul, Arzigul; Zhang, Danyang; Yu, Ping [College of Materials Science and Engineering, Sichuan University, Chengdu, 610064 (China)

2016-08-15

Multilayer thick films (∝4 μm) with compositional PbZr{sub 0.3}Ti{sub 0.7}O{sub 3}/LaNiO{sub 3} layers and one-layer PZT thick films were prepared on the silicon substrate by radio-frequency magnetron sputtering. PbZr{sub 0.3}Ti{sub 0.7}O{sub 3}/LaNiO{sub 3} multilayer thick film are characterized by highly preferential (100)-oriented growth and columnar microstructure due to alternately introducing LaNiO{sub 3} seeding layers. The effects of LaNiO{sub 3} layers on microstructure and electrical properties of PbZr{sub 0.3}Ti{sub 0.7}O{sub 3} thick films were investigated in detail. The results show that both PZT and PbZr{sub 0.3}Ti{sub 0.7}O{sub 3}/LaNiO{sub 3} multilayer thick film were pure perovskite crystalline phase. The PbZr{sub 0.3}Ti{sub 0.7}O{sub 3} film texture was dense and well adhered on the LaNiO{sub 3} layer. PbZr{sub 0.3}Ti{sub 0.7}O{sub 3}/LaNiO{sub 3} multilayer thick film possessed obvious enhanced dielectric properties compared with PZT thick film: ε{sub r} ∝2450 (10 kHz) and tanδ ∝0.02 (10 kHz). Rayleigh law was used to analysis the behavior of the enhanced dielectric properties and the pinched-shaped polarization-electric field hysteresis loops. The larger Rayleigh parameter, α ∝51.1408 cm kV{sup -1} (1 kHz) indicates the larger extrinsic contribution to permittivity and strong domain-wall-defect charge interaction. The leakage current behaviors of the multilayer thick film were also investigated in detail. (copyright 2016 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Study of the analytic quality in the determinations of Cr, Fe, Mn, Cu, Zn, Pb and Hg through conventional and nuclear analytical techniques in mosses of the MATV

International Nuclear Information System (INIS)

Caballero S, B.

2013-01-01

To evaluate the environmental risks of air pollution and to facilitate the decision-making for control, is necessary to have the capacity to generate data with analytical quality. A comparison between nuclear (Neutron activation analysis and total reflection X-ray fluorescence spectrometry) and no nuclear analytical techniques (atomic absorption spectrometry and inductively coupled plasma optical emission spectrometry) for simultaneous determination of metal content (Cr, Cu, Fe, Hg, Mn, Pb and Zn) in mosses from Metropolitan Area of the Toluca Valley (MATV) was performed. Epiphytic mosses (Fabriona ciliaris and Leskea angustata) were sampled in two campaigns, 16 sites (urban, transition and natural) and were prepared for each technique. The biological certified reference materials were used for the quality control and to evaluate accuracy, precision, linearity, detection and quantification limits. Results show that nuclear analytical techniques and no nuclear applied in chemical analysis of Cr, Cu, Fe, Hg, Mn, Pb and Zn in moss from MATV are comparable and therefore all of these can potentially be used for this purpose. However, if its considered both, the performance parameters and economic/operational characteristics is widely recommended inductively coupled plasma optical emission spectrometry, conventional analytical technique, which showed the highest analytical grade quality. Also were observed spatial and temporal variations in the concentrations of Cr, Cu, Fe, Hg, Mn, Pb and Zn in mosses from MATV and was discussed its potential origin. The urban sites had the highest concentration of anthropogenic elements as Cr, Cu, Fe, Hg, Pb and Zn because are strongly impacted by roads with high vehicle traffic. (Author)

The effect of intermetallic compound morphology on Cu diffusion in Sn-Ag and Sn-Pb solder bump on the Ni/Cu Under-bump metallization

Science.gov (United States)

Jang, Guh-Yaw; Duh, Jenq-Gong

2005-01-01

The eutectic Sn-Ag solder alloy is one of the candidates for the Pb-free solder, and Sn-Pb solder alloys are still widely used in today’s electronic packages. In this tudy, the interfacial reaction in the eutectic Sn-Ag and Sn-Pb solder joints was investigated with an assembly of a solder/Ni/Cu/Ti/Si3N4/Si multilayer structures. In the Sn-3.5Ag solder joints reflowed at 260°C, only the (Ni1-x,Cux)3Sn4 intermetallic compound (IMC) formed at the solder/Ni interface. For the Sn-37Pb solder reflowed at 225°C for one to ten cycles, only the (Ni1-x,Cux)3Sn4 IMC formed between the solder and the Ni/Cu under-bump metallization (UBM). Nevertheless, the (Cu1-y,Niy)6Sn5 IMC was observed in joints reflowed at 245°C after five cycles and at 265°C after three cycles. With the aid of microstructure evolution, quantitative analysis, and elemental distribution between the solder and Ni/Cu UBM, it was revealed that Cu content in the solder near the solder/IMC interface played an important role in the formation of the (Cu1-y,Niy)6Sn5 IMC. In addition, the diffusion behavior of Cu in eutectic Sn-Ag and Sn-Pb solders with the Ni/Cu UBM were probed and discussed. The atomic flux of Cu diffused through Ni was evaluated by detailed quantitative analysis in an electron probe microanalyzer (EPMA). During reflow, the atomic flux of Cu was on the order of 1016-1017 atoms/cm2sec in both the eutectic Sn-Ag and Sn-Pb systems.

A test of the stability of Cd, Cu, Hg, Pb and Zn profiles over two decades in lake sediments near the Flin Flon Smelter, Manitoba, Canada

Energy Technology Data Exchange (ETDEWEB)

Percival, J.B.; Outridge, P.M., E-mail: outridge@nrcan.gc.ca

2013-06-01

Lake sediments are valuable archives of atmospheric metal deposition, but the stability of some element profiles may possibly be affected by diagenetic changes over time. In this extensive case study, the stability of sedimentary Cd, Cu, Hg, Pb and Zn profiles was assessed in dated sediment cores that were collected in 2004 from four smelter-affected lakes near Flin Flon, Manitoba, which had previously been cored in 1985. Metal profiles determined in 1985 were in most cases clearly reproduced in the corresponding sediment layers in 2004, although small-scale spatial heterogeneity in metal distribution complicated the temporal comparisons. Pre-smelter (i.e. pre-1930) increases in metal profiles were likely the result of long-range atmospheric metal pollution, coupled with particle mixing at the 1930s sediment surface. However, the close agreement between key inflection points in the metal profiles sampled two decades apart suggests that metals in most of the lakes, and Hg and Zn in the most contaminated lake (Meridian), were stable once the sediments were buried below the surface mixed layer. Cadmium, Cu and Pb profiles in Meridian Lake did not agree as well between studies, showing evidence of upward remobilization over time. Profiles of redox-indicator elements (Fe, Mn, Mo and U) suggested that the rate of Mn oxyhydroxide recycling within sediment was more rapid in Meridian Lake, which may have caused the Cd, Cu and Pb redistribution. - Highlights: • Sedimentary Cd, Cu, Hg, Pb and Zn profiles in four lakes were mostly unchanged over 19 years. • In one lake, Cd, Cu and Pb profiles were offset relative to the originals. • The offset could indicate diagenetic upcore dispersal of these metals.

Mechanosynthesis of MFe2O4 (M = Co, Ni, and Zn Magnetic Nanoparticles for Pb Removal from Aqueous Solution

Directory of Open Access Journals (Sweden)

America R. Vazquez-Olmos

2016-01-01

Full Text Available Adsorption of Pb(II from aqueous solution using MFe2O4 nanoferrites (M = Co, Ni, and Zn was studied. Nanoferrite samples were prepared via the mechanochemical method and were characterized by X-ray powder diffraction (XRD, Fourier transform infrared spectroscopy (FTIR, micro-Raman, and vibrating sample magnetometry (VSM. XRD analysis confirms the formation of pure single phases of cubic ferrites with average crystallite sizes of 23.8, 19.4, and 19.2 nm for CoFe2O4, NiFe2O4, and ZnFe2O4, respectively. Only NiFe2O4 and ZnFe2O4 samples show superparamagnetic behavior at room temperature, whereas CoFe2O4 is ferromagnetic. Kinetics and isotherm adsorption studies for adsorption of Pb(II were carried out. A pseudo-second-order kinetic describes the sorption behavior. The experimental data of the isotherms were well fitted to the Langmuir isotherm model. The maximum adsorption capacity of Pb(II on the nanoferrites was found to be 20.58, 17.76, and 9.34 mg·g−1 for M = Co, Ni, and Zn, respectively.

Kinetic study on adsorption of Cr(VI), Ni(II), Cd(II) and Pb(II) ions from aqueous solutions using activated carbon prepared from Cucumis melo peel

Science.gov (United States)

Manjuladevi, M.; Anitha, R.; Manonmani, S.

2018-03-01

The adsorption of Cr(VI), Ni(II), Cd(II) and Pb(II), ions from aqueous solutions by Cucumis melo peel-activated carbon was investigated under laboratory conditions to assess its potential in removing metal ions. The adsorption behavior of metal ions onto CMAC was analyzed with Elovich, intra-particle diffusion rate equations and pseudo-first-order model. The rate constant of Elovich and intra-particle diffusion on CMAC increased in the sequence of Cr(VI) > Ni(II) > Cd(II) > Pb(II). According to the regression coefficients, it was observed that the kinetic adsorption data can fit better by the pseudo-first-order model compared to the second-order Lagergren's model with R 2 > 0.957. The maximum adsorption of metal ions onto the CMAC was found to be 97.95% for Chromium(VI), 98.78% for Ni(II), 98.55% for Pb(II) and 97.96% for Cd(II) at CMAC dose of 250 mg. The adsorption capacities followed the sequence Ni(II) ≈ Pb(II) > Cr(VI) ≈ Cd(II) and Ni(II) > Pb(II) > Cd(II) > Cr(VI). The optimum adsorption conditions selected were adsorbent dosage of 250 mg, pH of 3.0 for Cr(VI) and 6.0 for Ni(II), Cd(II) and Pb(II), adsorption concentration of 250 mg/L and contact time of 180.

Phytoextraction of Pb, Cr, Ni, and Zn using the aquatic plant Limnobium laevigatum and its potential use in the treatment of wastewater.

Science.gov (United States)

Arán, Daniela Silvina; Harguinteguy, Carlos Alfredo; Fernandez-Cirelli, Alicia; Pignata, María Luisa

2017-08-01

In order to study the bioaccumulation of Pb, Cr, Ni, and Zn and the stress response, the floating aquatic plant Limnobium laevigatum was exposed to increasing concentrations of a mixture of these metals for 28 days, and its potential use in the treatment of wastewater was evaluated. The metal concentrations of the treatment 1 (T1) were Pb 1 μg L -1 , Cr 4 μg L -1 , Ni 25 μg L -1 , and Zn 30 μg L -1 ; of treatment 2 (T2) were Pb 70 μg L -1 , Cr 70 μg L -1 , Ni 70 μg L -1 , and Zn 70 μg L -1 ; and of treatment 3 (T3) were Pb 1000 μg L -1 , Cr 1000 μg L -1 , Ni 500 μg L -1 , and Zn 100 μg L -1 , and there was also a control group (without added metal). The accumulation of Pb, Cr, Ni, and Zn in roots was higher than in leaves of L. laevigatum, and the bioconcentration factor revealed that the concentrations of Ni and Zn in the leaf and root exceeded by over a thousand times the concentrations of those in the culture medium (2000 in leaf and 6800 in root for Ni; 3300 in leaf and 11,500 in root for Zn). Thus, this species can be considered as a hyperaccumulator of these metals. In general, the changes observed in the morphological and physiological parameters and the formation of products of lipid peroxidation of membranes during the exposure to moderate concentrations (T2) of the mixture of metals did not cause harmful effects to the survival of the species within the first 14 days of exposure. Taking into account the accumulation capacity and tolerance to heavy metals, L. laevigatum is suitable for phytoremediation in aquatic environments contaminated with moderated concentrations of Cr, Ni, Pb, and Zn in the early stages of exposure.

A highly selective and sensitive photoswitchable fluorescent probe for Hg2+ based on bisthienylethene-rhodamine 6G dyad and for live cells imaging.

Science.gov (United States)

Xu, Li; Wang, Sheng; Lv, Yingnian; Son, Young-A; Cao, Derong

2014-07-15

A new photochromic diarylethene derivative bearing rhodamine 6G dimmer as a fluorescent molecular probe is designed and synthesized successfully. All the compounds are characterized by nuclear magnetic resonance and mass spectrometry. The bisthienylethene-rhodamine 6G dyad exhibit excellent phtochromism with reversibly color and fluorescence changes alternating irradiation with ultraviolet and visible light. Upon addition of Hg(2+), its color changes from colorless to red and its fluorescence is remarkably enhanced. Whereas other ions including K(+), Na(+), Ca(2+), Mg(2+), Fe(2+), Co(2+), Ni(2+), Cu(2+), Zn(2+), Mn(2+), Pb(2+), Ni(2+), Fe(3+), Al(3+), Cr(3+) and so on induce basically no spectral changes, which constitute a highly selective and sensitive photoswitchable fluorescent probe toward Hg(2+). Furthermore, by means of laser confocal scanning microscopy experiments, it is demonstrated that this probe can be applied for live cell imaging and monitoring Hg(2+) in living lung cancer cells with satisfying results, which shows its value of potential application in environmental and biological systems. Copyright © 2014 Elsevier B.V. All rights reserved.

Evaluation of potential of adsorption of U, Th, Pb, Zn and Ni by coconut fibers

International Nuclear Information System (INIS)

Monteiro, Raquel Almeida

2009-01-01

The residual biomass from agricultural activities has been evaluated as biosorbent for metals and organic composts from aqueous solutions, because of its adsorptive properties, low cost, abundance and to be a renewable resource. In this work, the efficiency of coir pith as biosorbent for the removal of U, Th, Pb, Zn e Ni ions from the aqueous solutions is presented. The coir pith is a by-product of the harvest of the coconut, a renewable natural source. The study was conducted by batch method. The influence of pH from 1 to 8, the dosage of the coir pith and the equilibrium time were studied. The adsorption of metal ions increased with the increase of pH and the dose. The Langmuir and Freundlich models were applied to describe the adsorption equilibrium isotherm. The kinetic process was studied using the pseudo-first order and pseudo-second order models. The Gibbs free energy was calculated. In the concentration range of 100 mg.L -1 - 500 mg.L -1 , the adsorption process was described better by the Langmuir equation for Pb 2+ and Zn 2+ ions and the Freundlich equation for UO 2 2 + , Th 4+ and Ni 2+ ions, and represented by the pseudo-second order model. The biosorption process for removal of metal ions from the solutions was considered spontaneous. The results were promising, showing perspectives of application of coir pith as biosorbent of U, Th, Pb, Zn and Ni ions in wastewater treatment processes. (author)

Formation of long-period stacking ordered structures in Mg88M5Y7 (M = Ti, Ni and Pb) casting alloys

International Nuclear Information System (INIS)

Jin, Qian-Qian; Fang, Can-Feng; Mi, Shao-Bo

2013-01-01

Highlights: •Apart from 18R-LPSO, 14H-LPSO structure was determined in the Mg-Ni-Y alloys. •The appearance of twin-related structure in 18R-LPSO structure results from the stacking faults in the stacking sequence of the closely packed planes. •A new (Pb, Mg) 2 Y phase with a body-centered orthorhombic structure was determined in the Mg-Pb-Y alloy. •No LPSO structures were found in the Mg-Pb-Y and Mg-Ti-Y casting alloys. -- Abstract: Formation of long-period stacking ordered (LPSO) structures is investigated in Mg 88 M 5 Y 7 (M = Ti, Ni and Pb) casting alloys by means of electron microscopy and X-ray diffraction. In the Mg 88 Ni 5 Y 7 casting alloy, 14H-LPSO structure is observed in a small amount, which coexists with 18R-LPSO structure. The appearance of stacking faults in 18R-LPSO structure results in twin-related structure in the stacking sequence of the closely packed planes. A new (Pb, Mg) 2 Y phase with a body-centered orthorhombic structure is determined in the Mg 88 Pb 5 Y 7 alloy. No LPSO structures are found in the Mg 88 Pb 5 Y 7 and Mg 88 Ti 5 Y 7 casting alloys. In terms of the atomic radius and heat of mixing, the formation ability of LPSO structure in the present alloys is discussed

Nuclear structure from N ≅ Z to N > Z - 100Sn, 78Ni, 208Pb

International Nuclear Information System (INIS)

Grawe, H.; Gorska, M.; Rejmund, M.; Pfuetzner, M.; Brown, B.A.; Maier, K.H.

1998-07-01

The single particle (hole) energies in 100 Sn, as extrapolated by a shell model analysis of the neighbouring nuclei, show a remarkable similarity to those in 56 Ni, one major shell lower. This is borne out in nearly identical I π =2 + excitation energies, implying E(2 + )≅3 MeV in 100 Sn, and a large neutron effective E2 charge e≥1.6e. In contrast a small proton polarisation charge δe≤0.3e is found, pointing to a large isovector charge. In 104 Sn for the first time in this region strong E3 transitions with B(E3)≥17 Wu were identified, indicating E(3 - )≅3 MeV in 100 Sn. Isomer spectroscopy beyond 68 Ni following fragmentation of a 60.3 A MeV 86 Kr beam has provided first evidence on the neutron polarisation charge and the occupation of the νg 9/2 orbital beyond N=40, which is at variance with shell model calculations using realistic interactions. The N=40 subshell effect seen in E(2 + ) is not borne out in 2n separation energies. On the other hand the νg 9/2 -f 5/2 splitting of single quasiparticle energies in Ni, Fe and Cr isotopes, as deduced from M2 isomers, give no hint for deformation at Z 208 Pb a number of new isomers were observed in the fragmentation of a 1000 A MeV 238 U beam, while 3 - excitations on high spin configurations in and adjacent to 208 Pb were identified in inelastic collisions of 208 Pb+ 208 Pb. E2 and E3 strengths from stretched configurations are compared to model expectations. (orig.)

Determination of Cd, Hg, Pb and Tl in coal and coal fly ash slurries using electrothermal vaporization inductively coupled plasma mass spectrometry and isotopic dilution

Energy Technology Data Exchange (ETDEWEB)

Maia, S.M.; Pozebon, D.; Curtius, A.J. [Univ. Federal de Santa Catarina, Florianopolis, SC (Brazil)

2003-07-01

A method has been investigated for the determination of Cd, Hg, Pb and Tl in coal and in coal fly ash, using slurry sampling electrothermal vaporization inductively coupled plasma mass spectrometry and isotope dilution. The slurry, 25 mg ml{sup -1}, was prepared by mixing the powdered sample (less than or equal to 36 - 45 mm) with acid solutions (nitric acid for coal and nitric and hydrofluoric acids for coal fly ash) and submitting the mixture to an ultrasonic agitation, letting it stand afterwards in a water bath at 60{sup o}C for 2 h. An ultrasonic probe was used to homogenize the slurry in the autosampler cup just before its introduction into the graphite tube. The best conditions were determined regarding analyte sensitivity, furnace temperature program, amount of modifier, acid concentration, gas flow rate and particle size. For Hg, the pyrolysis stage was omitted and a low vaporization temperature was used (450 - 1000{sup o}C); the residual matrix was eliminated in the first step of the following cycle. The modifiers used were: Pd for Cd and Tl; Au, Ir or Pd for Hg; Ir or Pd for Pb. The accuracy of the method was checked by analyzing six certified coal reference materials (SARM 20, SARM 19, BCR No. 40, BCR No. 180, BCR No. 181 and NIST 1630a) and one certified coal fly ash (NIST 1633b). With one exception (Hg in BCR No. 180), the found concentrations were typically within 95% confidence interval of the certified values, or close enough to the recommended values, as long as the samples were ground to a small enough particle size. The limits of detection were typically around 0.08 {mu}g g{sup -1}, 0.03 {mu}g g{sup -1}, 1 {mu}g g{sup -1} and 0.02 {mu}g g{sup -1} for Cd, Hg, Pb and Tl, respectively. The precision was also adequate with relative standard deviations of usually < 5%.

Contamination assessment of heavy metals in the soils around Khouzestan Steel Company (Ni, Mn, Pb, Fe, Zn, Cr)

International Nuclear Information System (INIS)

Hormozi Nejad, F.; Rastmanesh, F.; Zarasvandi, A.

2016-01-01

The highest concentrations were found at soil samples 4 and 12. Comparison of heavy metals concentration with unpolluted soil standard indicated that, concentrations of Cr, Zn, Fe, Ni and Pb is higher than that of unpolluted soil standard. In general, Manganese, Chromium, Zinc and Lead are the most important elements that are found in emissions of steel plants. The soil samples near the steel plant and downwind direction have much higher pollution level. The results showed that Mn, Pb and Zn is related to human activity and Cr have geogenic source and Fe and Ni have both geogenic and anthropogenic source in the study area in the city of Ahwaz.

Toxic elements (As, Se, Cd, Hg, Pb) and their mineral and technogenic formations in the snow cover in the vicinity of the industrial enterprises of Tomsk

International Nuclear Information System (INIS)

Talovskaya, A V; Filimonenko, E A; Osipova, N A; Lyapina, E E; Azikov, E G Y

2014-01-01

Snow samples were collected in four industrial areas of Tomsk where brickworks, factories for the production of reinforced concrete structures, machine repair industries and local boilers, petrochemical plant and thermal power station are located. Study of insoluble fraction of aerosols in snow and melted snow water was performed to determine the contents of the emissions from these facilities. The insoluble fraction of aerosols in snow is aerosol particles deposited on snow cover. As, Se, Cd, Hg, Pb concentration was analyzed by inductively coupled plasma mass spectrometry (ICP-MS). Mineral modes of the elements were determined by scanning electron microscope. It was found the snow cover is mainly polluted by As, Se, Cd, Hg, Pb in the thermal power station impact area, by As – in the brickworks impact area, by Se – in the impact area of densely located factories for the production of reinforced concrete structures, machine repair industries and local boilers. The research results show that the mineral modes of As are associated with arsenopyrite, of Pb – with galena in the insoluble fraction of aerosols in snow

High Efficient Nanocomposite for Removal of Heavy Metals (Hg2+ and Pb2+ from Aqueous Solution

Directory of Open Access Journals (Sweden)

M. Ebadi

2016-01-01

Full Text Available In current work, CdS/black carbon nanocomposites were successfully synthesized with the aid of chestnut and cadmium nitrate as the starting reagents. Besides, the effects of preparation parameters such as reaction time, and precursor concentration on the morphology of products and removal of heavy metals (Hg+2, Pb+2 were studied by scanning electron microscopy images and batch adsorption mode. CdS/black carbon nanocomposite introduced as new and high efficient system for removal of heavy metal ions. The as-synthesized products were characterized by powder X-ray diffraction, scanning electron microscopy, and spectra energy dispersive analysis of X-ray.

Accumulation of Pb, Hg, Cd, Se, Sc, Cr, Rb, Fe, Zn, Co in the plants and sludges of the Lake Balaton

International Nuclear Information System (INIS)

Teherani, D.K.; Altmann, H.; Wallisch, G.

1981-01-01

Various plants (Ceratophyllum demersum, Potamogeton pectinatus, Myriophyllum spicatum) and mud samples taken from Lake Balaton (Paloznak, Balatonfuezfoe) in June 1978 were analyzed for Se, Cr, Sc, Rb, Fe, Zn, Co by neutron activation analysis and for Cd, Pb, Hg by atomic absorption spectrometry. The concentration values found for Se ranged between 0.25-1.2 ppm (plant) and 0.99-1.47 ppm (mud), for Cr 1.6-6 ppm (plant) and 4.85-40.75 ppm (mud), for Sc 0.4-0.75 ppm (plant) and 3.25-5.87 ppm (mud), for Rb 6.75-16 ppm (plant) and 17-48.75 ppm (mud), for Fe 636.7-4491 ppm (plant) and 11034-12057 ppm (mud), for Zn 20.5-38.5 ppm (plant) and 29.75-41.75 ppm (mud), for Co 0.77-4.75 ppm (plant) and 4.87-5.5 ppm (mud), for Pb 4.5-23.5 ppm (plant) and 18-28 ppm (mud), for Cd <0.03 ppm (plant, mud), for Hg <0.01-0.07 ppm (plant) and 0.04-0.08 ppm (mud). (author)

Hg{sup 2+}-induced self-assembly of a naphthalimide derivative by selective 'turn-on' monomer/excimer emissions

Energy Technology Data Exchange (ETDEWEB)

Wanichacheva, Nantanit, E-mail: wanichacheva.nantanit@gmail.com [Department of Chemistry, Faculty of Science, Silpakorn University, Nakorn Pathom 73000 (Thailand); Prapawattanapol, Narupon [Petrochemistry and Polymer Science Program, Faculty of Science, Chulalongkorn University, Bangkok 10330 (Thailand); Sanghiran Lee, Vannajan [Department of Chemistry, Faculty of Science, University of Malaya 50603, Kuala Lumpur (Malaysia); Grudpan, Kate [Department of Chemistry, Center for Innovation in Chemistry, Faculty of Science, and Center of Excellence in Innovation for Analytical Science and Technology, Chiang Mai 50200 (Thailand); Petsom, Amorn [Research Centre for Bioorganic Chemistry, Department of Chemistry, Faculty of Science, Chulalongkorn University, Bangkok 10330 (Thailand)

2013-02-15

A novel fluorescent sensor bearing two naphthalimide fluorophores based on 2-(3-(2-aminoethylsulfanyl)propylsulfanyl)ethanamine, 1, was readily synthesized for the recognition of Hg{sup 2+}. The sensitive and selective binding behaviors of 1 were investigated by fluorescence spectroscopy. Sensor 1 selectively binds Hg{sup 2+} by exhibiting OFF-ON fluorescence enhancement behaviors of the monomer and excimer bands. The sensor provides excellent Hg{sup 2+}-selectivity in the presence of high concentrations of competitive ions, particularly Cu{sup 2+} and Pb{sup 2+} as well as Na{sup +}, K{sup +}, Mn{sup 2+}, Cd{sup 2+}, Ni{sup 2+}, Ca{sup 2+}, Li{sup +}, Zn{sup 2+} and Co{sup 2+}, with an available detection limit of 2.1 Multiplication-Sign 10{sup -7} M or 42 ppb. - Highlights: Black-Right-Pointing-Pointer Multidentate sulfide-containing ligand bounded to naphthalimide as new Hg{sup 2+} sensor. Black-Right-Pointing-Pointer Sensor is prepared by a straightforward two-step synthesis. Black-Right-Pointing-Pointer Sensor shows high sensitivity and selectivity to Hg{sup 2+} with detection limit of 42 ppb. Black-Right-Pointing-Pointer Hg{sup 2+}-binding is indicated by fluorescence enhancement Black-Right-Pointing-Pointer Sensor 'turns-on' both monomeric and excimer emissions by the addition of Hg{sup 2+}.

Analysis of Pb, Cd, Cr and Ni concentrations in types of cabbage marketed in Hamedan City

Directory of Open Access Journals (Sweden)

S Sobhanardakani

2015-02-01

Full Text Available Today, due to the accumulation of heavy metals in vegetables irrigated with wastewater and treated with sewage sludge has become increasing concern in the field of food safety and health of consumers. Therefore this study was conducted for analysis of Pb, Cd, Cr and Ni concentrations of 3 types of cabbage marketed in Hamedan City during 2013. For this purpose after buying 30 samples of each species of cabbage and then acid digestion of the samples according to standard methods, elements (Pb, Cd, Cr and Ni were determined using ICP-OES (Varian, 710-ES, Australia. All statistical analyses were performed using the SPSS statistical package. The results showed that mean concentrations of Pb, Cd, Cr and Ni in Cabbage samples were 15.53±3.43, 59.33±5.35, 2.22±1.61 and 14.97±2.83 mg/kg, respectively; mean concentrations of these elements in red cabbage samples were 23.03±5.89, 37.53±4.21, 13.33±3.24 and 15.03±3.04 mg/kg, respectively; and mean concentrations of elements in broccoli samples were 8.00±3.63, 45.90±5.86, 8.20±3.39 and 16.93±3.08 mg/kg, respectively. Also comparison of the mean concentrations of evaluated metals in specimens with FAO/WHO permissible limits showed that significant difference (p

Determination of Cd, Hg, Pb and Se in sediments slurries by isotopic dilution calibration ICP-MS after chemical vapor generation using an on-line system or retention in an electrothermal vaporizer treated with iridium

International Nuclear Information System (INIS)

Vieira, Mariana Antunes; Ribeiro, Anderson Schwingel; Dias, Lucia Felicidade; Curtius, Adilson Jose

2005-01-01

A method for the determination of Cd, Hg, Pb and Se in sediments reference materials by slurry sampling chemical vapor generation (CVG) using isotopic dilution (ID) calibration and detection by inductively coupled plasma mass spectrometry (ICP-MS) is proposed. Two different systems were used for the investigation: an on-line flow injection system (FI-CVG-ICP-MS) and an off-line system with in situ trapping electrothermal vaporization (CVG-ETV-ICP-MS). About 100 mg of the reference material, ground to a particle size ≤50 μm, was mixed with acid solutions (aqua regia, HF and HCl) in an ultrasonic bath. The enriched isotopes 111 Cd, 198 Hg, 206 Pb and 77 Se were then added to the slurry in an adequate amount in order to produce an altered isotopic ratio close to 1. For the on-line system, a standing time for the slurry of 12 h before measurement was required, while for the batch system, no standing time is needed to obtain accurate results. The conditions for the formation of the analyte vapor were optimized for the evaluated systems. The following altered isotope ratios were measured: 111 Cd/ 114 Cd, 198 Hg/ 199 Hg, 206 Pb/ 208 Pb e 77 Se/ 82 Se. The obtained detection limits in the on-line system, in μg g -1 , were: Cd: 0.15; Hg: 0.09; Pb: 6.0 and Se: 0.03. Similar detection limits were obtained with the system that uses the ETV: 0.21 for Hg, 6.0 for Pb and 0.06 μg g -1 for Se. No signal for Cd was obtained in this system. One estuarine, two marine and two river certified sediments were analyzed to check the accuracy. The obtained values by both systems were generally in agreement with the certified concentrations, according to the t-test for a confidence level of 95%, demonstrating that isotope equilibration was attained in the slurries submitted to a chemical vapor generation procedure and detection by ICP-MS. The relative standard deviations were lower than 10%, adequate for slurry analysis. The almost quantitative analytes extractions to the aqueous phase

Adsorption of Cu(II), Hg(II), and Ni(II) ions by modified natural wool chelating fibers

International Nuclear Information System (INIS)

Monier, M.; Ayad, D.M.; Sarhan, A.A.

2010-01-01

The graft copolymerization of ethyl acrylate (EA) onto natural wool fibers initiated by potassium persulphate and Mohr's salt redox initiator system in limited aqueous medium was carried out in heterogeneous media. Ester groups of the grafted copolymers were partially converted into hydrazide function groups followed by hydrazone formation through reaction with isatin. Also the application of the modified fibers for metal ion uptake was studied using Cu(II), Hg(II) and Ni(II). The modified chelating fibers were characterized using FTIR spectroscopy, SEM and X-ray diffraction.

KANDUNGAN LOGAM BERAT (Hg, Cd, dan Pb DALAM AIR TANAH PADA PERUMAHAN TIPE KECIL DI JABOTABEK

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Athena Athena

2012-09-01

Full Text Available A survey of heavy metals (Hg, Cd, Pb in drinking water at small and very small houses was conducted in Jakarta, Bogor, Tangerang and Bekasi (Jabotabek, in 1992. The purpose of this study was to get information about water quality and environmental condition of water sources at low cost housing and very low cost housing in Jabotabek. Forty to sixty water samples were taken from each location and analyzed by Atomic Absorption Spectrophotometer. The mercury concentration was analyzed using Cold Vapor Technique, whereas Cd and Pb were analized using The Air-acetylene method. Water samples were collected in dry season and rainy season. Interview of the owners of the house and of environmental observation of the water sources were done to get information about the condition of drinking water sources. The highest concentration of mercury detected in Jakarta was in the rainy season (2.50 mg/l. Cadmium and Lead were detected in Bogor, (Cd: 0.26 mg/l in the rainy season and Pb : 0.16 mg/l in dry season. However 41.5% water samples from Jakarta were exceeding the mercury concentration standard, 25.4% water samples from Bogor were exceeding cadmium concentration standard, and 41.1% water samples from Bogor were exceeding lead concentration standard Heavy metals concentration in drinking water at Bekasi and Tangerang were relatively lower than Bogor and Jakarta. The environmental condition of shallow wells in Bekasi and Tangerang were also better than Bogor and Jakarta.

Folic acid functionalized silver nanoparticles with sensitivity and selectivity colorimetric and fluorescent detection for Hg2+ and efficient catalysis.

Science.gov (United States)

Su, Dongyue; Yang, Xin; Xia, Qingdong; Zhang, Qi; Chai, Fang; Wang, Chungang; Qu, Fengyu

2014-09-05

In this research, folic acid functionalized silver nanoparticles (FA-AgNPs) were selected as a colorimetric and a 'turn on' fluorescent sensor for detecting Hg(2+). After being added into Hg(2+), AgNPs can emit stable fluorescence at 440 nm when the excitation wavelength is selected at 275 nm. The absorbance and fluorescence of the FA-AgNPs could reflect the concentration of the Hg(2+) ions. Thus, we developed a simple, sensitive analytical method to detect Hg(2+) based on the colorimetric and fluorescence enhancement of FA-AgNPs. The sensor exhibits two linear response ranges between absorbance and fluorescence intensity with Hg(2+) concentration, respectively. Meanwhile, a detection limit of 1 nM is estimated based on the linear relationship between responses with a concentration of Hg(2+). The high specificity of Hg(2+) with FA-AgNPs interactions provided the excellent selectivity towards detecting Hg(2+) over other metal ions (Pb(2+), Mg(2+), Zn(2+), Ni(2+), Cu(2+), Co(2+), Ca(2+), Mn(2+), Fe(2+), Cd(2+), Ba(2+), Cr(6+) and Cr(3+)). This will provide a simple, effective and multifunctional colorimetric and fluorescent sensor for on-site and real-time Hg(2+) ion detection. The proposed method can be applied to the analysis of trace Hg(2+) in lake water. Additionally, the FA-AgNPs can be used as efficient catalyst for the reduction of 4-nitrophenol and potassium hexacyanoferrate (III).

Efeito da temperatura, pH e vestígios de Hg2+ e Pb2+ na acti­vidade de desidrogenases e urease num solo da região de Évora Effect of temperature, pH and Hg2+ and Pb2+ traces in dehydrogenaseand urease activities of a soil from Évora region

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M. R. Martins

2010-01-01

Full Text Available As actividades das enzimas no solo são um importante indicador da sua qualida­de. Neste estudo procedeu-se à caracteri­zação da actividade enzimática de desi­drogenases (EC 1.1.1 e da urease (EC 3.5.1.5 de um solo sob Olea europeae L. da região de Évora. As constantes cinéti­cas Km e Vmáx, foram determinadas usando como substratos o cloreto de p­-iodonitrotetrazolio (INT e a ureia, res­pectivamente. Foi avaliado o efeito nas referidas actividades provocado pelo pH, temperatura e vestígios de Hg2+ e de Pb2+. As actividades máximas obtiveram-se a pH = 8,5 e 40 ºC, com Km= 0,5 mM e Vmáx = 5,4 µmol min-1 g-1, para a activida­de de desidrogenases e a pH = 10 e 37 ºC, com Km = 25,7 mM e Vmáx = 2,0x10-2 µmol min-1 g-1, para a urease. Estas acti­vidades foram inibidas por diferentes concentrações de Hg2+, mas apenas a acti­vidade da urease foi inibida pelo Pb2+. Estes resultados são comparáveis com os referidos na literatura para estes enzimas.Enzyme activities are often used as in­dicator of soil quality. This study reports on dehydrogenase (EC 1.1.1 and urease (EC 3.5.1.5 activities of a soil under Olea europaea L. from Évora region. Kinetic constants Km and Vmax were determined using p-iodonitrotetrazolium chloride (INT and urea, respectively. Effects of pH, temperature and Hg2+ and Pb2+ traces on both activities were determined. Maximal activity was obtained at pH = 8.5 and 40ºC, Km = 0.5 mM and Vmax=5,4µmol min-1 g-1 , for dehydro­genase and at pH = 10 and 37 ºC, Km = 25.7 mM and Vmax = 2.0x10-2 µmol min-1 g-1, for urease. These activities were in­hibited by different concentrations of Hg2+, but only the urease activity was in­hibited by Pb2+. Results of this study are comparable to those reported in the litera­ture for these enzymes.

SEPARATION OF Fe (III, Cr(III, Cu(II, Ni(II, Co(II, AND Pb(II METAL IONS USING POLY(EUGENYL OXYACETIC ACID AS AN ION CARRIER BY A LIQUID MEMBRANE TRANSPORT METHOD

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La Harimu

2010-06-01

Full Text Available Fe (III, Cr(III, Cu(II, Ni(II, Co(II, and Pb(II  metal ions had been separated using poly(eugenyl oxyacetic acid as an ion carrier by bulk liquid membrane transport method. The effect of pH, polyeugenyl oxyacetic acid ion carrier concentration, nitric acid concentration in the stripping solution, transport time, and metal concentration were optimized. The result showed that the optimum condition for transport of metal ions was at pH 4 for ion Fe(III and at pH 5 for Cr(III, Cu(II, Ni(II, Co(II, and Pb(II ions. The carrier volumes were optimum with concentration of 1 x 10-3 M at 7.5 mL for Cr(III, Cu (II,  Ni(II, Co(II ions and at 8.5 mL for Fe(III and Pb(II ions. The concentration of HNO3 in stripping phase was optimum at 2 M for Fe(III and Cu(II ions, 1 M for Cr(III, Ni(II and Co(II ions, and 0.5 M for Pb(II ion. The optimum transport times were 36 h for Fe(III and Co(II ions, and 48 h for Cr(III, Cu (II, Ni(II, and Pb(II ions. The concentration of metal ions accurately transported were 2.5 x 10-4 M for Fe(III and Cr(III ions, and 1 M for Cu (II, Ni(II, Co(II, and Pb(II ions. Compared to other metal ions the transport of Fe(III was the highest with selectivity order of Fe(III > Cr(III > Pb(II > Cu(II > Ni(II > Co(II. At optimum condition, Fe(III ion was transported through the membrane at 46.46%.   Keywords: poly(eugenyl oxyacetic acid, transport, liquid membrane, Fe (III, Cr(III, Cu(II, Ni(II, Co(II, and Pb(II ions

[Sources, pollution statue and potential ecological risk of heavy metals in surface sediments of Aibi Lake, Northwest China].

Science.gov (United States)

Zhang, Zhao-Yong; Abuduwaili, Jilili; Jiang, Feng-Qing

2015-02-01

In this paper, the surface sediment samples were harvested from Aibi Lake, and total contents of 8 heavy metals ( Cu, Pb, Zn, As, Hg, Cr, Ni and Cd) were determined. Then the sources, pollution statue, and potential ecological risk were analyzed by using multiple analysis methods. The results show that: (1) The order of the skewness for these 8 heavy metals is: Hg > Cd > Pb > Zn > As > Cu > Cr > Ni. (2) Multivariate statistical analysis shows that 8 heavy metals can be classified to 2 principle components, among which PC1 ( Cd, Pb, Hg and Zn) is man-made source factor and mainly came from all kinds of waste of agriculture; PC2 ( Cu, Ni, Cr and As) is natural source and was mainly controlled by the background of the natural geography of this area. (3) Accumulation of index evaluation results show that the order of pollution degree values of 8 heavy metals in surface sediments of Aibi Lake is: Cd > Hg > Pb > Zn > As > Cu > Ni > Cr. In all samples, heavy metals Hg, Cd and Pb all belong to low and partial moderate pollution statue, while Zn, As, Cr, Ni and Cu belong to no pollution statue in majority samples. (4) Potential ecological risk assessment results show that the potential ecological risk of heavy metals in surface sediments of Aibi Lake mainly caused by Cd, Hg and Pb, and they accounting for 42.6%, 28.6% and 24.0% of the total amount, respectively, among which Cd is the main ecological risk factor, followed by Hg and Pb. In all samples, the potential ecological risk index values (RI) of 8 heavy metals are all lower than 150, and they are all at low ecological risk levels. However, this research also shows that there have high content of Cd and Pb in the sediment. Therefore, we should make long-term monitoring of the lake environment.

Adsorption of Cu(II), Hg(II), and Ni(II) ions by modified natural wool chelating fibers

Energy Technology Data Exchange (ETDEWEB)

Monier, M., E-mail: monierchem@yahoo.com [Chemistry Department, Drexel University, Philadelphia, PA (United States); Chemistry Department, Faculty of Science, Mansoura University, Mansoura (Egypt); Ayad, D.M.; Sarhan, A.A. [Chemistry Department, Faculty of Science, Mansoura University, Mansoura (Egypt)

2010-04-15

The graft copolymerization of ethyl acrylate (EA) onto natural wool fibers initiated by potassium persulphate and Mohr's salt redox initiator system in limited aqueous medium was carried out in heterogeneous media. Ester groups of the grafted copolymers were partially converted into hydrazide function groups followed by hydrazone formation through reaction with isatin. Also the application of the modified fibers for metal ion uptake was studied using Cu(II), Hg(II) and Ni(II). The modified chelating fibers were characterized using FTIR spectroscopy, SEM and X-ray diffraction.

Adsorption of Cu(II), Hg(II), and Ni(II) ions by modified natural wool chelating fibers.

Science.gov (United States)

Monier, M; Ayad, D M; Sarhan, A A

2010-04-15

The graft copolymerization of ethyl acrylate (EA) onto natural wool fibers initiated by potassium persulphate and Mohr's salt redox initiator system in limited aqueous medium was carried out in heterogeneous media. Ester groups of the grafted copolymers were partially converted into hydrazide function groups followed by hydrazone formation through reaction with isatin. Also the application of the modified fibers for metal ion uptake was studied using Cu(II), Hg(II) and Ni(II). The modified chelating fibers were characterized using FTIR spectroscopy, SEM and X-ray diffraction. 2009 Elsevier B.V. All rights reserved.

Cost effective and shape controlled approach to synthesize

Indian Academy of Sciences (India)

It is found that NiOs exhibited the excellent performance for the removal of Hg(II), Pb(II) and Cd(II) from aqueous solution. The equilibrium adsorption data of Hg(II), Pb(II) and Cd(II) on the as-prepared NiOs were analyzed by Langmuir and Freundlich models, suggesting that the Langmuir model provides the better ...

Effect of Na, Ca and pH on simultaneous uptake of Cd, Cu, Ni, Pb, and Zn in the water flea Daphnia magna measured using stable isotopes

International Nuclear Information System (INIS)

Komjarova, I.; Blust, R.

2009-01-01

The present study investigates the effects of Na + , Ca 2+ and pH on the kinetics of Cd, Cu, Ni, Pb, and Zn uptake in Daphnia magna at low exposure concentrations measured using a stable isotope technique. Using experimental data the uptake rate constants were calculated for each metal individually on the basis of total metal concentrations. The copper uptake was not significantly affected by variations in chemical composition of the test medium. Calcium had a suppressing effect on the uptake of Cd, Ni, Pb and Zn. Specifically, Cd and Ni uptake rate constants decreased with increases in calcium concentrations from 0.1 to 2.5 mM. The uptake of Zn and Pb was significantly suppressed only at 2.5 mM Ca. The effect of sodium was less clear. There was no effect of varying sodium concentrations on the Ni uptake rate constants. Cd and Pb showed an increase in uptake rate constants at elevated sodium concentrations (2-8 mM Na + for Cd and 8 mM Na + for Pb). A bell-shaped response on increasing Na + concentrations was observed for Zn with a maximum value of uptake rate constant at the middle value (2 mM Na + ). Variation in pH of the medium affected Cd, Ni and Zn uptake processes. When Daphnia were exposed to acidic conditions (pH 6), the Cd and Ni uptake rate constants were the highest, while similarly low values were observed at neutral and basic conditions. In contrast, the uptake rates of Zn were linearly increasing with increasing pH of the medium.

Picomolar selective detection of mercuric ion (Hg{sup 2+}) using a functionalized single plasmonic gold nanoparticle

Energy Technology Data Exchange (ETDEWEB)

Song, Hyeon Don; Choi, Inhee; Yang, Young In; Hong, Surin; Lee, Suseung; Yi, Jongheop [School of Chemical and Biological Engineering, Institute of Chemical Processes, Seoul National University, Seoul 151-742 (Korea, Republic of); Kang, Taewook, E-mail: xinly601@snu.ac.kr, E-mail: iniini79@snu.ac.kr, E-mail: netmo00@snu.ac.kr, E-mail: pell2004@snu.ac.kr, E-mail: jazz1863@snu.ac.kr, E-mail: twkang@sogang.ac.kr, E-mail: jyi@snu.ac.kr [Department of Chemical and Biomolecular Engineering, Sogang University, Seoul 121-742 (Korea, Republic of)

2010-04-09

A highly sensitive method for the selective detection and quantification of mercuric ions (Hg{sup 2+}) using single plasmonic gold nanoparticle (GNP)-based dark-field microspectroscopy (DFMS) is demonstrated. The method is based on the scattering property of a single GNP that is functionalized with thiolated molecules, which is altered when analytes bind to the functionalized GNP. The spectral resolution of the system is 0.26 nm and a linear response to Hg{sup 2+} was found in the dynamic range of 100 pM-10 {mu}M. The method permits Hg{sup 2+} to be detected at the picomolar level, which is a remarkable reduction in the detection limit, considering the currently proscribed Environmental Protection Agency regulation level (10 nM, or 2 ppb) and the detection limits of other optical methods for detecting Hg{sup 2+} (recently approx. 1-10 nM). In addition, Hg{sup 2+} can be sensitively detected in the presence of Cd{sup 2+}, Pb{sup 2+}, Cu{sup 2+}, Zn{sup 2+} and Ni{sup 2+}, which do not interfere with the analysis. Based on the findings reported herein, it is likely that single-nanoparticle-based metal ion sensing can be extended to the development of other chemo- and biosensors for the direct detection of specific targets in an intracellular environment as well as in environmental monitoring.

Noncompetitive and Competitive Adsorption of Heavy Metals in Sulfur-Functionalized Ordered Mesoporous Carbon.

Science.gov (United States)

Saha, Dipendu; Barakat, Soukaina; Van Bramer, Scott E; Nelson, Karl A; Hensley, Dale K; Chen, Jihua

2016-12-14

In this work, sulfur-functionalized ordered mesoporous carbons were synthesized by activating the soft-templated mesoporous carbons with sulfur bearing salts that simultaneously enhanced the surface area and introduced sulfur functionalities onto the parent carbon surface. XPS analysis showed that sulfur content within the mesoporous carbons were between 8.2% and 12.9%. The sulfur functionalities include C-S, C═S, -COS, and SO x . SEM images confirmed the ordered mesoporosity within the material. The BET surface areas of the sulfur-functionalized ordered mesoporous carbons range from 837 to 2865 m 2 /g with total pore volume of 0.71-2.3 cm 3 /g. The carbon with highest sulfur functionality was examined for aqueous phase adsorption of mercury (as HgCl 2 ), lead (as Pb(NO 3 ) 2 ), cadmium (as CdCl 2 ), and nickel (as NiCl 2 ) ions in both noncompetitive and competitive mode. Under noncompetitive mode and at a pH greater than 7.0 the affinity of sulfur-functionalized carbons toward heavy metals were in the order of Hg > Pb > Cd > Ni. At lower pH, the adsorbent switched its affinity between Pb and Cd. In the noncompetitive mode, Hg and Pb adsorption showed a strong pH dependency whereas Cd and Ni adsorption did not demonstrate a significant influence of pH. The distribution coefficient for noncompetitive adsorption was in the range of 2448-4000 mL/g for Hg, 290-1990 mL/g for Pb, 550-560 mL/g for Cd, and 115-147 for Ni. The kinetics of adsorption suggested a pseudo-second-order model fits better than other models for all the metals. XPS analysis of metal-adsorption carbons suggested that 7-8% of the adsorbed Hg was converted to HgSO 4 , 14% and 2% of Pb was converted to PbSO 4 and PbS/PbO, respectively, and 5% Cd was converted to CdSO 4 . Ni was below the detection limit for XPS. Overall results suggested these carbon materials might be useful for the separation of heavy metals.

Relationships between metal concentrations in great tit nestlings and their environment and food

International Nuclear Information System (INIS)

Dauwe, Tom; Janssens, Ellen; Bervoets, Lieven; Blust, Ronny; Eens, Marcel

2004-01-01

Metal concentrations (Ag, As, Cd, Cu, Hg, Ni, Pb, Zn) were determined in the feathers and excreta of nestling great tits (Parus major), in their main invertebrate prey (Lepidoptera larvae) and in vegetation samples, all collected from four sites along a pollution gradient. Metal contamination in vegetation samples increased significantly towards the pollution source. The Ag, As, Hg, Ni and Pb concentrations in food samples were significantly higher at the site closest to the pollution source compared to the other three sites. Great tit nestlings from the site closest to the pollution source had significantly higher concentrations of Ag, As, Hg and Pb in their excreta than did nestlings at the other three sites. For five metals (Ag, As, Cu, Ni and Pb), we found concentrations in caterpillars to be significantly positively correlated with vegetation samples. We also found clear significant positive correlations between excreta and caterpillars for Ag, As, Hg and Pb and between feathers and caterpillars for As and Pb. Our data suggest that excreta are a good monitor for the presence and concentrations of non-essential metals in the food and the environment of passerine birds

Dissolved trace metals (Ni, Zn, Co, Cd, Pb, Al, and Mn) around the Crozet Islands, Southern Ocean

Science.gov (United States)

Castrillejo, Maxi; Statham, Peter J.; Fones, Gary R.; Planquette, Hélène; Idrus, Farah; Roberts, Keiron

2013-10-01

A phytoplankton bloom shown to be naturally iron (Fe) induced occurs north of the Crozet Islands (Southern Ocean) every year, providing an ideal opportunity to study dissolved trace metal distributions within an island system located in a high nutrient low chlorophyll (HNLC) region. We present water column profiles of dissolved nickel (Ni), zinc (Zn), cobalt (Co), cadmium (Cd), lead (Pb), aluminium (Al), and manganese (Mn) obtained as part of the NERC CROZEX program during austral summer (2004-2005). Two stations (M3 and M1) were sampled downstream (north) of Crozet in the bloom area and near the islands, along with a control station (M2) in the HNLC zone upstream (south) of the islands. The general range found was for Ni, 4.64-6.31 nM; Zn, 1.59-7.75 nM; Co, 24-49 pM; Cd, 135-673 pM; Pb, 6-22 pM; Al, 0.13-2.15 nM; and Mn, 0.07-0.64 nM. Vertical profiles indicate little island influence to the south with values in the range of other trace metal deprived regions of the Southern Ocean. Significant removal of Ni and Cd was observed in the bloom and Zn was moderately correlated with reactive silicate (Si) indicating diatom control over the internal cycling of this metal. Higher concentrations of Zn and Cd were observed near the islands. Pb, Al, and Mn distributions also suggest small but significant atmospheric dust supply particularly in the northern region.

Graphite furnace atomic absorption spectrometric determination of Ni and Pb in diesel and gasoline samples stabilized as microemulsion using conventional and permanent modifiers

International Nuclear Information System (INIS)

Matos Reyes, Mariela N.; Campos, Reinaldo C.

2005-01-01

A procedure for the graphite furnace atomic absorption spectrometric determination of Ni and Pb in diesel and gasoline samples was developed. Sample stabilization was necessary because of evident analyte losses that occurred immediately after sampling. Excellent long-term sample stabilization was observed by mixing different organic solvents with propan-1-ol and 50% vol/vol HNO 3 at a 3.3:6.5:1 volume ratio. For Pb, efficient thermal stabilization was obtained using aqueous Pd-Mg modifier as well as for Ir as permanent modifier. The drying temperature and ramp rate influenced the sensitivity obtained for Ni, and had to be carefully optimized. Taking this into account, the same sensitivity was attained in all investigated organic media stabilized as microemulsion. Thus, calibration with microemulsions prepared with a single organic solvent was possible, using aqueous or organic stock solutions. Commercial gasoline and diesel samples were directly analyzed after stabilization as microemulsion and by comparative UOP procedures. n-Hexane microemulsions were used for calibration, and good agreement was obtained between the results using the proposed and comparative procedures. Typical coefficients of variation (n = 6) ranged from 1% to 4%, and from 1% to 3% for Ni and Pb, respectively. Detection limits (k = 3) in the original gasoline or diesel samples, derived from 10 blank measurements, were 4.5 and 3.6 μg l -1 for Ni and Pb, respectively, comfortably below the values found in the analyzed samples

Ecophysiological and seasonal variations in Cd, Pb, Zn, and Ni concentrations in the leaves of urban deciduous trees in Istanbul

International Nuclear Information System (INIS)

Baycu, Guelriz; Tolunay, Doganay; Ozden, Hakan; Guenebakan, Suereyya

2006-01-01

The concentrations of Cd, Pb, Zn and Ni were measured in the leaves of 7 species of deciduous trees, from the urban sites of Istanbul, in both the Spring and Autumn seasons. We detected some differences in the heavy metal concentrations of the control and urban site samples of identical species. Highest concentrations of Cd were detected in Populus, Pb in Aesculus and Robinia, Zn in Populus, and Ni in Robinia and Fraxinus. Lowest chlorophyll content and highest peroxidase (POD) activity was found in the urban site samples of Acer. We have found a positive correlation between the increase in the POD activity and the Pb concentration in Populus. Generally, the tree species investigated in this study, are considered to have different tolerance levels to heavy metal pollution. The data obtained show that the chlorophyll content and the POD activity may be used as heavy metal stress biomarkers in the urban trees. - Ecophysiological changes in the urban trees may be used as heavy metal stress biomarkers

Thiol-functionalized polysilsesquioxane as efficient adsorbent for adsorption of Hg(II) and Mn(II) from aqueous solution

International Nuclear Information System (INIS)

Niu, Yuzhong; Qu, Rongjun; Liu, Xiguang; Mu, Lei; Bu, Baihui; Sun, Yuting; Chen, Hou; Meng, Yangfeng; Meng, Lina; Cheng, Lin

2014-01-01

Highlights: • PMPSQ was promising adsorbent for the removal of Hg(II) and Mn(II). • The adsorption kinetics followed the pseudo-second-order model. • The adsorption isotherms can be described by the monolayer Langmuir model. • The adsorption was controlled by film diffusion and chemical ion-exchange mechanism. - Abstract: Thiol-functionalized polysilsesquioxane was synthesized and used for the adsorption of Hg(II) and Mn(II) from aqueous solution. Results showed that the optimal pH was about 6 and 5 for Hg(II) and Mn(II), respectively. Adsorption kinetics showed that the adsorption equilibriums were established within 100 min and followed pseudo-second-order model. Adsorption isotherms revealed that the adsorption capacities increased with the increasing of temperature. The adsorption was found to be well described by the monolayer Langmuir isotherm model and took place by chemical ion-exchange mechanism. The thermodynamic properties indicated the adsorption processes were spontaneous and endothermic nature. Selectively adsorption showed that PMPSQ can selectively adsorb Hg(II) from binary ion systems in the presence of the coexistent ions Mn(II), Cu(II), Pb(II), Co(II), and Ni(II). Based on the results, it is concluded that PMPSQ had comparable high adsorption efficiency and could be potentially used for the removal of Hg(II) and Mn(II) from aqueous solution

Teores de As, Pb, Cd e Hg e fertilidade de solos da região do Vale do Alto Guaporé, sudoeste do estado de Mato Grosso Contents of As, Pb, Cd e Hg and fertility of soils of Vale do Alto Guapore region, south-west of Mato Grosso state

Directory of Open Access Journals (Sweden)

Maria Aparecida Pereira Pierangeli

2009-03-01

Full Text Available O diagnóstico da fertilidade e teores de elementos-traço (ETs em solos é importante, pois estes dados são escassos na literatura para áreas de transição Pantanal-Cerrado-Floresta Amazônica. Esse trabalho avaliou diversos parâmetros relacionados à fertilidade, teores biodisponíveis de Fe, Mn, Zn, Cu e B e semitotais de As, Cd, Hg e Pb de solos do Vale do Alto Guaporé, região sudoeste do estado de Mato Grosso. Foram coletadas amostras de solos (0-0,20 e 0,20-0,40 m de profundidade em áreas de vegetação nativa (VN, pastagem (AP, cultura anual (CA e garimpo de ouro (G. As amostras foram analisadas conforme métodos de rotina para avaliação da fertilidade do solo e ETs pelo método SW-3051A e os resultados médios comparados com os valores de referência de qualidade (VRQ para solos estipulados pela Companhia de Tecnologia de Saneamento Ambiental (CETESB. Teores mais elevados de As e Hg foram verificados em VN e G com médias, respectivamente, iguais a 43,9 e 101,13 para o As; e 0,12 e 0,14 mg kg-1 para o Hg. Exceto Pb, vários locais de amostragem apresentaram teores dos ETs superiores ao VRQ: 46% em VN; 60% em G; 28% em CA; e 44% em AP, para o As; 20,8; 50; 55; e 22% em VN, G, CA e AP, respectivamente, para o Cd; 75; 65 e 67% das áreas de VN, G e CA e AP, respectivamente, para o Hg. A saturação por bases foi alta (60-80% em 51,5% das amostras, enquanto o P foi baixo em todas áreas. Valores de referência de qualidade de solo para o As e Hg devem ser estipulados para solos dessa região, tendo em vista que os teores observados em áreas nativas foram superiores ao VRQ.The fertility and trace elements diagnosis of soils is important for agricultural and environmental purposes, because there is little data available on the Pantanal-Cerrado-Floresta Amazônica transitional areas. This work evaluated many parameters relative to the fertility, Fe, Mn, Zn, Cu and B bioavailability, and total content of As, Cd, Hg and Pb in soils of

193Hg collective oblate band with Ex>5.7 MeV

International Nuclear Information System (INIS)

Roy, N.; Henry, E.A.; Becker, J.A.

1993-01-01

Rotational bands in the neutron-deficient Pb nuclei 192,194,196-201 Pb have been reported recently. Band members are connected by L = 1 transitions, with crossover L = 2 transitions observed at the higher γ-ray energies. Regular and irregular patterns of γ-ray energies are observed. Conversion coefficients determined from intensity balance suggest the L = 1 transitions are M1. The bands have generally been interpreted as collective oblate, involving deformation aligned high-j proton configurations such as π(s 1/2 -2 h 9/2 i 13/2 ), and rotation aligned i 13/2 -n neutrons. Evidence for a similar band in 193 Hg has been obtained. 193 Hg was populated in the reaction 176 Yb( 22 Ne,5n) at E i ( 22 Ne) = 110 MeV. Reaction γ rays were detected with the Ge detector array HERA. A new 'collective' structure was observed with E x >5.7 MeV. States of the structure extend from I≥47/2 to I +10, and they decay with competing dipole and quadrupole transitions. The ratio B(M1)/B(E2), ∼ 2μ 2 /(e b) 2 , is approximately 10x lower in 193 Hg than in the Pb bands. The lowest member is produced with ∼20% of the 193 Hg cross section. Evidence for a similar band in 196 Hg will be presented at this meeting

Metal pollution (Pb, Zn, Ni and Cr) in air, road and soil sediment in a high traffic area; Contaminacion por metales (Pb, Zn, Ni y Cr) en aire, sedimentos viales y suelo en una zona de alto trafico vehicular

Energy Technology Data Exchange (ETDEWEB)

Manchado, Anali; Garcia, Neyma; Garcia, Cezar; Acosta, Lorena; Cordova, Alberto; Linares, Maria; Giraldoth, Debora [Centro de Investigaciones CEDEGAS, Facultad de Ingenieria, Universidad del Zulia, Maracaibo (Venezuela)]. E-mail: analimachado@yahoo.com; amachadop@luz.edu.ve; Velasquez, Harvi [Facultad Experimental de Ciencias, Universidad del Zulia, Maracaibo (Venezuela)

2008-11-15

Due to the important health effects of inhalable particles (PM10) and its associated metals, levels of four trace metals (Pb, Ni, Zn, Cr) generated by mobile sources with variable toxicity incorporated to PM10 atmospheric samples in a high density traffic area were evaluated. Samples were collected at two different sites (being considered as emission and dispersion areas) during a dry-wet season period, using a low volume air sampler equipped with quartz fiber filters; after an acid extraction, samples were analyzed by atomic absorption spectrometry. PM10 concentrations were two times higher in the emission area than in the dispersion area for both climatic regimens, but exhibited a better correlation between sites during the dry season. All the elements showed statistically significant differences between monitoring sites. On the other hand, when the total sampling period for PM10 is compared for all the tested metals, significant differences between sites and between meteorological seasons can be appreciated. The Venezuelan air quality standard for Pb was not exceeded, but a mean concentration of 1.13 {mu}g/m{sup 3} -very close to Venezuelan and USEPA standard- was obtained at the emission site. Nevertheless, Pb and Ni reported levels for both locations were above the Organizacion Mundial de la Salud (OMS) allowed limit during the whole sampling period. Further, the statistical analysis demonstrated the selection of the monitoring areas was adequate, confirming that motor vehicles are the main emission source of these atmospheric pollutants. [Spanish] Debido a la importancia del efecto sobre la salud de las particulas inhalables PM10 y los metales asociados a ellas, se evaluaron los niveles de cuatro metales traza (Pb, Ni, Zn y Cr) generados por fuentes moviles de dichas particulas, en sedimentos viales y suelo en una zona de alta densidad vehicular. Las muestras fueron colectadas en los sitios considerados como de emision y dispersion durante las epocas de

Evaluation on the stability of Hg in ABS disk CRM during measurements by wavelength dispersive X-ray fluorescence spectrometry.

Science.gov (United States)

Ohata, Masaki; Kidokoro, Toshihiro; Hioki, Akiharu

2012-01-01

The stability of Hg in an acrylonitrile-butadiene-styrene disk certified reference material (ABS disk CRM, NMIJ CRM 8116-a) during measurements by wavelength dispersion X-ray fluorescence (WD-XRF) analysis was evaluated in this study. The XRF intensities of Hg (L(α)) and Pb (L(α)) as well as the XRF intensity ratios of Hg (L(α))/Pb (L(α)) observed under different X-ray tube current conditions as well as their irradiation time were examined to evaluate the stability of Hg in the ABS disk CRM. The observed XRF intensities and the XRF intensity ratios for up to 32 h of measurements under 80 mA of X-ray tube current condition were constant, even though the surface of the ABS disk CRM was charred by the X-ray irradiation with high current for a long time. Moreover, the measurements on Hg and Pb in the charred disks by an energy dispersive XRF (ED-XRF) spectrometer showed constant XRF intensity ratios of Hg (L(α))/Pb (L(α)). From these results, Hg in the ABS disk CRM was evaluated to be sufficiently stable for XRF analysis.

Apportioning global and non-global components of mercury deposition through (210)Pb indexing.

Science.gov (United States)

Lamborg, Carl H; Engstrom, Daniel R; Fitzgerald, William F; Balcom, Prentiss H

2013-03-15

Our previous work has documented a correlation between Hg concentrations and (210)Pb activity measured in wet deposition that might be used to help apportion sources of Hg in precipitation. Here we present the results of a 27-month precipitation collection effort using co-located samplers for Hg and (210)Pb designed to assess this hypothesis. Study sites were located on the east and west coasts of North America, in the continental interior, and on the Florida Peninsula. Relatively high variability in Hg/(210)Pb ratios was found at all sites regionally and seasonally (e.g., overall: 0.99-9.13ngdpm(-1)). The ratio of average volume-weighted Hg concentrations and (210)Pb activities showed consistent trends (higher in impacted area), with Glacier Bay in southeast Alaska, exhibiting the lowest value. Assuming that Glacier Bay represents a benchmark for a site with no regional contribution, we estimate less than 50% of the Hg input was "global" at the Seattle and Florida sites. Differences in Hg/(210)Pb in wet deposition could be due to either a regional/local source contribution of Hg, or a regional/local enhancement in the removal of Hg from the atmosphere (i.e., oxidants), however, this approach is not capable of discerning between these two possibilities. Thus, this method of source apportionment represents an estimate of the maximal amount of Hg contributed by regional sources and may be limited in regions of deep convective mixing. Copyright © 2012 Elsevier B.V. All rights reserved.

Study on lead transportation in air-water-paddy system with 210Pb as tracer

International Nuclear Information System (INIS)

Li Shuding; Zhang Hairong; Ma Xuejun

1987-08-01

With 210 PbCl 2 as tracer, a research into lead sources in brown rice, lead distribution in soil and rice, lead chemical forms in soil and their change with time, availability of soil for rice and effect of soil pH on the Pb adsorption was carried out in air-water-paddy system near cities and towns located upper and middle reaches of Liaohe River, northeastern China. Test soil was light acid meadow brown soil. The Pb proportions in rice grain derived from the soil, airborne dust and irrigation water and the transportation pathway to brown rice were investigated. Transportation coefficients of Pb in the system were determined by tracer experiment. It was indicated that the Pb concentration in rice root, the Pb concentration and its distribution in the soil are main factors effecting Pb transportation to rice. Based on the simulation test, mathematical model for computing soil environmental capacity of Pb in the system is put forward. The soil environmental capacity of Pb computed is 1600 - 1700 ppm, i.e. 3.6 - 3.8 t/ha. The computed result was in agreement with the observed. The mathematical model was also used to compute soil enviromental capacity of those heavy metal corresponding respectively with 203 Hg, 115+115m Cd, 65 Zn, 51 Cr, 65 Ni, 60 Co etc

Copper separation using modified active carbon before the polarographic determination of Pb, Cd, Ni, Zn and Fe in wastes

International Nuclear Information System (INIS)

Rubel, S.; Lada, Z.M.; Golimowski, J.

1977-01-01

The investigations on the selective separation of Pb 2+ , Cd 2+ , Ni 2+ , Zn 2+ and Fe 3+ ions from the excess of copper were carried out. For this purpose active carbon modified by Na-diethyldithiocarbamate was used. The manner of DDTK-Na deposition on active carbon has been elaborated. The influence of pH was investigated and it was found that at pH 1(HNO 3 ) copper ions are quantitavely bound on modified carbon whereas other ions (Pb 2+ , Cd 2+ , Ni 2+ , Zn 2+ and Fe 3+ ) remain in the solution and can be determined polarographically. The elaborated method was applied to the determination of mentioned ions in the samples of wastes containing even 100-fold excess of copper. The concentration of copper can not exceed 100 mg/dm 3 . (author)

Comparison of a static and a dynamic in vitro model to estimate the bioaccessibility of As, Cd, Pb and Hg from food reference materials Fucus sp. (IAEA-140/TM) and Lobster hepatopancreas (TORT-2)

Energy Technology Data Exchange (ETDEWEB)

Torres-Escribano, Silvia [Instituto de Agroquimica y Tecnologia de Alimentos (IATA-CSIC), Apdo. 73, 46100, Burjassot, Valencia (Spain); Denis, Sylvain; Blanquet-Diot, Stephanie [Clermont Universite, Universite d' Auvergne, Centre de Recherche en Nutrition Humaine Auvergne, ERT 18, Conception ingenierie et developpement de l' aliment et du medicament, BP 10448, F-63000 Clermont-Ferrand (France); Calatayud, Marta [Instituto de Agroquimica y Tecnologia de Alimentos (IATA-CSIC), Apdo. 73, 46100, Burjassot, Valencia (Spain); Barrios, Laura [Departamento de Informatica Cientifica (SGAI-CSIC), C/ Pinar 19, 28006 Madrid (Spain); Velez, Dinoraz, E-mail: deni@iata.csic.es [Instituto de Agroquimica y Tecnologia de Alimentos (IATA-CSIC), Apdo. 73, 46100, Burjassot, Valencia (Spain); Alric, Monique [Clermont Universite, Universite d' Auvergne, Centre de Recherche en Nutrition Humaine Auvergne, ERT 18, Conception ingenierie et developpement de l' aliment et du medicament, BP 10448, F-63000 Clermont-Ferrand (France); Montoro, Rosa [Instituto de Agroquimica y Tecnologia de Alimentos (IATA-CSIC), Apdo. 73, 46100, Burjassot, Valencia (Spain)

2011-01-01

Bioaccessibility, the fraction of an element solubilized during gastrointestinal digestion and available for absorption, is a factor that should be considered when evaluating the health risk of contaminants from food. Static and dynamic models that mimic human physiological conditions have been used to evaluate bioaccessibility. This preliminary study compares the bioaccessibility of arsenic (As), cadmium (Cd), lead (Pb) and mercury (Hg) in two food certified reference materials (CRMs) (seaweed: Fucus sp., IAEA-140/TM; Lobster hepatopancreas: TORT-2), using two in vitro gastrointestinal digestion methods: a static method (SM) and a dynamic multicompartment method (TIM-1). There are significant differences (p < 0.05) between the bioaccessible values of As, Cd, Pb and Hg obtained by SM and TIM-1 in the two CRMs. The specific form in which the elements studied are present in the CRM may help to explain the bioaccessibility values obtained. - Research Highlights: {yields}Data are reported for As, Cd, Pb and Hg bioaccessibility from food CRMs. {yields}The static and TIM-1 methods give significantly different bioaccessibility values. {yields}The possible influence of speciation on bioaccessibility is discussed. {yields}To improve bioaccessibility quality data, food reference materials are needed.

Comparison of a static and a dynamic in vitro model to estimate the bioaccessibility of As, Cd, Pb and Hg from food reference materials Fucus sp. (IAEA-140/TM) and Lobster hepatopancreas (TORT-2)

International Nuclear Information System (INIS)

Torres-Escribano, Silvia; Denis, Sylvain; Blanquet-Diot, Stephanie; Calatayud, Marta; Barrios, Laura; Velez, Dinoraz; Alric, Monique; Montoro, Rosa

2011-01-01

Bioaccessibility, the fraction of an element solubilized during gastrointestinal digestion and available for absorption, is a factor that should be considered when evaluating the health risk of contaminants from food. Static and dynamic models that mimic human physiological conditions have been used to evaluate bioaccessibility. This preliminary study compares the bioaccessibility of arsenic (As), cadmium (Cd), lead (Pb) and mercury (Hg) in two food certified reference materials (CRMs) (seaweed: Fucus sp., IAEA-140/TM; Lobster hepatopancreas: TORT-2), using two in vitro gastrointestinal digestion methods: a static method (SM) and a dynamic multicompartment method (TIM-1). There are significant differences (p < 0.05) between the bioaccessible values of As, Cd, Pb and Hg obtained by SM and TIM-1 in the two CRMs. The specific form in which the elements studied are present in the CRM may help to explain the bioaccessibility values obtained. - Research Highlights: →Data are reported for As, Cd, Pb and Hg bioaccessibility from food CRMs. →The static and TIM-1 methods give significantly different bioaccessibility values. →The possible influence of speciation on bioaccessibility is discussed. →To improve bioaccessibility quality data, food reference materials are needed.

Characteristics of equilibrium, kinetics studies for adsorption of Hg(II), Cu(II), and Ni(II) ions by thiourea-modified magnetic chitosan microspheres

International Nuclear Information System (INIS)

Zhou Limin; Wang Yiping; Liu Zhirong; Huang Qunwu

2009-01-01

Magnetic chitosan microspheres were prepared and chemically modified with thiourea (TMCS) for adsorption of metal ions. TMCS obtained were investigated by means of X-ray diffraction (XRD), IR, magnetic properties and thermogravimetric analysis (TGA). The adsorption properties of TMCS toward Hg 2+ , Cu 2+ , and Ni 2+ ions were evaluated. Various factors affecting the uptake behavior such as contact time, temperature, pH and initial concentration of the metal ions were investigated. The kinetics was evaluated utilizing the pseudo-first-order, pseudo-second-order, and the intra-particle diffusion models. The equilibrium data were analyzed using the Langmuir, Freundlich, and Tempkin isotherm models. The adsorption kinetics followed the mechanism of the pseudo-second-order equation for all systems studied, evidencing chemical sorption as the rate-limiting step of adsorption mechanism and not involving a mass transfer in solution. The best interpretation for the equilibrium data was given by Langmuir isotherm, and the maximum adsorption capacities were 625.2, 66.7, and 15.3 mg/g for Hg 2+ , Cu 2+ , and Ni 2+ ions, respectively. TMCS displayed higher adsorption capacity for Hg 2+ in all pH ranges studied. The adsorption capacity of the metal ions decreased with increasing temperature. The metal ion-loaded TMCS with were regenerated with an efficiency of greater than 88% using 0.01-0.1 M ethylendiamine tetraacetic acid (EDTA)

Evaluation of three endemic Mediterranean plant species Atriplex halimus, Medicago lupulina and Portulaca oleracea for Phytoremediation of Ni, Pb and Zn

Science.gov (United States)

Chami, Ziad Al; Amer, Nasser; Bitar, Lina Al; Mondelli, Donato; Dumontet, Stefano

2013-04-01

The success of phytoremediation depends upon the identification of suitable plants species that hyperaccumulate/tolerate heavy metals and produce large amounts of biomass. In this study, three endemic Mediterranean plant species Atriplex halimus, Medicago lupulina and Portulaca oleracea, were grown hydroponically to assess their potential use in phytoremediation of Ni, Pb and Zn and biomass production. The objective of this research is to improve phytoremediation procedures by searching for a new endemic Mediterranean plant species which can be used for phytoremediation of low/moderate contamination in the Mediterranean arid and semiarid conditions and bioenergy production. The hydroponics experiment was carried out in a growth chamber using half strength Hoagland's solution as control (CTR) and 5 concentrations for Pb and Zn (5, 10, 25, 50 and 100 mg L-1) and 3 concentrations for Ni (1, 2, and 5 mg L-1). Complete randomized design with five replications was adopted. Main growth parameters (shoot and root dry weight, shoot and root length and chlorophyll content) were determined. Shoots and roots were analyzed for their metals contents. Some interesting contributions of this research are: (i) plant metal uptake efficiency ranked as follows: A. halimus > M. lupulina > P. oleracea, whereas heavy metal toxicity ranked as follows: Ni > Zn > Pb, (ii) none of the plant species was identified as hyperaccumulator, (iii) Atriplex halimus and Medicago lupulina can accumulate Ni, Pb and Zn in their roots, (iv) translocate small fraction to their above ground biomass, and (v) indicate moderate pollution levels of the environment. In addition, as they are a good biomass producer, they can be used in phytostabilisation of marginal lands and their above ground biomass can be used for livestock feeding as well for bioenergy production.

The differential cross section and polarization for the elastic scattering of 2.9 MeV neutrons by Fe, Cu, I, Hg and Pb

International Nuclear Information System (INIS)

Galloway, R.B.; Waheed, A.

1979-01-01

Simultaneous measurements are presented of the angular dependence of polarization due to elastic scattering and of the elastic differential cross section for 2.9 MeV neutrons. The angular range covered is 20 0 to 160 0 for samples of Fe, Cu, I, Hg and Pb. The measurements are compared with the results of combining optical model and Hauser-Feshbach calculations. The optical model calculations were performed using 'global fit' parameters as well as with parameters suggested previously for the particular nuclei. The Hauser-Feshbach calculations were performed both with and without the level width fluctuation correction. It is clear that the calculations made without the level width fluctuation correction provide a better fit to the data for Fe, Cu, I and Hg and only for Pb does inclusion of the level width fluctuation correction provide a better fit. These optical model parameter sets are shown not to be very successful in fitting both differential cross-section and polarization data. The results of searches for the parameters which give the best fit for the data are presented. These parameter sets are compared with one another and with the results of 8 and 11 MeV neutron scattering studies for trends in the variation of the parameters. (Auth.)

Modeling the adsorption of metal ions (Cu 2+, Ni 2+, Pb 2+) onto ACCs using surface complexation models

Science.gov (United States)

Faur-Brasquet, Catherine; Reddad, Zacaria; Kadirvelu, Krishna; Le Cloirec, Pierre

2002-08-01

Activated carbon cloths (ACCs), whose efficiency has been demonstrated for microorganics adsorption from water, were here studied in the removal of metal ions from aqueous solution. Two ACCs are investigated, they are characterized in terms of porosity parameters (BET specific surface area, percentage of microporosity) and chemical characteristics (acidic surface groups, acidity constants, point of zero charge). A first part consists in the experimental study of three metal ions removal (Cu 2+, Ni 2+ and Pb 2+) in a batch reactor. Isotherms modeling by Freundlich and Brunauer-Emmett-Teller (BET) equations enables the following adsorption order: Cu 2+>Ni 2+>Pb 2+ to be determined for adsorption capacities on a molar basis. It may be related to adsorbates characteristics in terms of electronegativity and ionic radius. The influence of adsorbent's microporosity is also shown. Adsorption experiments carried out for pH values ranging from 2 to 10 demonstrate: (i) an adsorption occurring below the precipitation pH; (ii) the strong influence of pH, with a decrease of electrostatic repulsion due to the formation of less charged hydrolyzed species coupled with a decrease of activated carbon surface charge as pH increases. The second part focuses on the modeling of adsorption versus the pH experimental data by the diffuse layer model (DLM) using Fiteql software. The model is efficient to describe the system behavior in the pH range considered. Regarding complexation constants, they show the following affinity for ACC: Pb 2+>Cu 2+>Ni 2+. They are related to initial concentrations used for the three metal ions.

The Impact of a Nickel-Copper Smelter on Concentrations of Toxic Elements in Local Wild Food from the Norwegian, Finnish, and Russian Border Regions.

Science.gov (United States)

Hansen, Martine D; Nøst, Therese H; Heimstad, Eldbjørg S; Evenset, Anita; Dudarev, Alexey A; Rautio, Arja; Myllynen, Päivi; Dushkina, Eugenia V; Jagodic, Marta; Christensen, Guttorm N; Anda, Erik E; Brustad, Magritt; Sandanger, Torkjel M

2017-06-28

Toxic elements emitted from the Pechenganickel complex on the Kola Peninsula have caused concern about potential effects on local wild food in the border regions between Norway, Finland and Russia. The aim of this study was to assess Ni, Cu, Co, As, Pb, Cd, and Hg concentrations in local wild foods from these border regions. During 2013-2014, we collected samples of different berry, mushroom, fish, and game species from sites at varying distances from the Ni-Cu smelter in all three border regions. Our results indicate that the Ni-Cu smelter is the main source of Ni, Co, and As in local wild foods, whereas the sources of Pb and Cd are more complex. We observed no consistent trends for Cu, one of the main toxic elements emitted by the Ni-Cu smelter; nor did we find any trend for Hg in wild food. Concentrations of all investigated toxic elements were highest in mushrooms, except for Hg, which was highest in fish. EU maximum levels of Pb, Cd, and Hg were exceeded in some samples, but most had levels considered safe for human consumption. No international thresholds exist for the other elements under study.

Evaluation of harmful heavy metal (Hg, Pb and Cd reduction using Halomonas elongata and Tetragenococcus halophilusfor protein hydrolysate product

Directory of Open Access Journals (Sweden)

Ruttiya Asksonthon

2016-04-01

Full Text Available Background: Many health claims surrounding antioxidative, antihypertensive and anti-inflammatory properties have been addressed in natural protein hydrolysates, including fermented fish. Besides being sold as animal feed, tuna viscera is used for the production of fermented products like fish sauce and Tai pla, fermented viscera. However, toxic heavy metals including Hg, Pb and Cd have been found in various food items, particularly within the internal organs of tuna. Therefore, the consumption of fermented tuna viscera containing heavy metal involves health risks. Consequently, the detoxification and reduction of these toxic elements are relevant and important issues, particularly with the use of their bacterial cells and metabolic products. Halomonas elongatais a moderately halophilic bacterium which has the ability to remove heavy metal, and is normally found in hypersaline environments. Tetragenococcus halophilusis a moderately halophilic lactic acid bacterium and probiotic which is found in fermented food products, such as fish sauce, shrimp paste, and fermented fish. Some scientific studies have reported using T. halophilus improves amino acid profiles and desirable volatile compounds, in addition to reducing biogenic amine content in fish sauce product. Therefore, it was hypothesized that using H.elongata and T. halophilus could reduce heavy metal content and improve the organoleptic quality of fermented fish viscera product (Tai pla. Objective: This present work attempted to determine the growth characteristic of H. elongataand T. halophilus reared at various NaCl concentrations:10, 15, 20 and 25%. Consequently, heavy metal reduction using these microorganisms reared at optimum NaCl concentration was evaluated. Methods: H. elongate and T. halophilus were reared in saline nutrient broth (SNB and de Man, Rogosa and Sharpe (MRS-broth added with NaCl at concentration 10, 15, 20 and 25%, respectively. Cultures at each NaCl content were added

Hg removal and the effects of coexisting metals in forward osmosis and membrane distillation.

Science.gov (United States)

Wu, Chia-Yu; Chen, Shiao-Shing; Zhang, Dai-Zhou; Kobayashi, Jun

2017-06-01

In this study, we investigate the rejection of Hg, Cd, and Pb and the effect of coexisting metals on Hg removal through forward osmosis (FO) and membrane distillation (MD) in order to establish a more effective water treatment process. The results of our laboratory experiment indicate that more than 97% of the rejection for each metal is achieved through the FO system, and this rejection is the highest among previous studies using membrane filtrations. Moreover, we examine the matrix effect of the coexisting Cd and Pb on the rejection of Hg in the FO system. Hg 2+ rejection increases with increase in the concentration of the coexisting metals. Furthermore, we study the effect of the Hg concentration and the water temperature on rejection of Hg 2+ . Indeed, the rejection of Hg 2+ is achieved above 95% under any condition. However, approximately 1-10 ppb Hg from the feed solution remains in the draw solution due to permeation. Therefore, we use a FO-MD hybrid system. Approximately 100% rejection of Hg 2+ and a stable water flux are achieved. Thus, the FO-MD hybrid system is considered an important alternative to previous studies using membrane filtration for heavy metals removal.

Comment on ''Energy partition in near-barrier strongly damped collisions 58Ni+208Pb''

International Nuclear Information System (INIS)

Viola, V.E.; Kwiatkowski, K.; Breuer, H.; Planeta, R.

1993-01-01

Chatterjee et al. [Phys. Rev. C 44, R2249 (1991)] report that the sharing of dissipated energy in the 58 Ni + 208 Pb reaction at E/A=6.5 MeV is not influenced appreciably by the direction and magnitude of net charge (and mass) transfer. We point out that neither this conclusion nor one arguing for a correlation between mass flow and excitation energy division is supported by the data and analysis presented in their communication

Distribution and accumulation of Cd, Cu, Hg, Pb and Zn in the surface sediments of El Tobari Lagoon, central-East Gulf of California: An ecosystem associated with agriculture and aquaculture activities.

Science.gov (United States)

Jara-Marini, M E; Tapia-Alcaraz, J N; Dumer-Gutiérrez, J A; García-Rico, L; García-Hernández, J; Páez-Osuna, F

2013-01-01

The purpose of this research is to provide a comprehensive assessment of the concentration levels and spatial variability of cadmium (Cd), copper (Cu), mercury (Hg), lead (Pb) and zinc (Zn) in El Tobari Lagoon in surface sediments during two seasons for several geochemical variables that could explain the observed heavy metal variability. Seventy-two surface sediments samples were collected in 12 different sites of the El Tobari Lagoon. Sediment samples were dried and subjected to acid extraction using a microwave system and five metals (Cd, Cu, Hg, Pb and Zn) were measured using atomic adsorption spectrometry. A certificate sediment material and blanks were used as quality control purposes. The enrichment factor (EF) and the index of geoaccumulation (Igeo) were calculated as index of metals contamination for the sediments, using aluminum as the conservative element. The five metals examined in sediments from El Tobari Lagoon exhibited a linear correlation with Al as result of the large specific surface areas of these sediment components and the chemical affinities between them. The metals contents in sites of the El Tobari Lagoon were variable, and Cd, Cu and Hg presented a seasonal behavior. The enrichment factor and index of geoaccumulation analysis indicated that Cd and Hg exhibited a certain extent (EF for Cd ranged from 4.10 to 10.29; EF for Hg ranged from 2.77 to 12.89) of anthropogenic pollution, while Cu showed sporadic (EF ranged from 0.43 to 2.54) anthropogenic contamination. The highest concentrations of Cd, Cu and Hg were found in the sites that regularly received discharge effluents from agriculture and aquaculture.

Sorption properties of the activated carbon-zeolite composite prepared from coal fly ash for Ni(2+), Cu(2+), Cd(2+) and Pb(2+).

Science.gov (United States)

Jha, Vinay Kumar; Matsuda, Motohide; Miyake, Michihiro

2008-12-15

Composite materials of activated carbon and zeolite have been prepared successfully by activating coal fly ash (CFA) by fusion with NaOH at 750 degrees C in N(2) followed by hydrothermal treatments under various conditions. Uptake experiments for Ni(2+), Cu(2+), Cd(2+) and Pb(2+) were performed with the materials thus obtained from CFA. Of the various composite materials, that were obtained by hydrothermal treatment with NaOH solution (ca. 4M) at 80 degrees C (a composite of activated carbon and zeolite X/faujasite) proved to be the most suitable for the uptake of toxic metal ions. The relative selectivity of the present sorbents for the various ions was Pb(2+)>Cu(2+)>Cd(2+)>Ni(2+), with equilibrium uptake capacities of 2.65, 1.72, 1.44 and 1.20mmol/g, respectively. The sorption isotherm was a good fit to the Langmuir isotherm and the sorption is thought to progress mainly by ion exchange with Na(+). The overall reaction is pseudo-second order with rate constants of 0.14, 0.17, 0.21 and 0.20Lg/mmol min for the uptake of Pb(2+), Cu(2+), Cd(2+) and Ni(2+), respectively.

Comprehensive risk assessment and source identification of selected heavy metals (Cu, Cd, Pb, Zn, Hg, As) in tidal saltmarsh sediments of Shuangtai Estuary, China.

Science.gov (United States)

Liu, Chang-Fa; Li, Bing; Wang, Yi-Ting; Liu, Yuan; Cai, Heng-Jiang; Wei, Hai-Feng; Wu, Jia-Wen; Li, Jin

2017-10-06

Heavy metals do not degrade and can remain in the environment for a long time. In this study, we analyzed the effects of Cu, Cd, Pb, Zn, Hg, and As, on environmental quality, pollutant enrichment, ecological hazard, and source identification of elements in sediments using data collected from samples taken from Shuangtai tidal wetland. The comprehensive pollution indices were used to assess environmental quality; fuzzy similarity analysis and geoaccumulation index were used to analyze pollution accumulation; correlation matrix, principal component analysis, and clustering analysis were used to analyze pollution source; environmental risk index and ecological risk index were used to assess ecological risk. The results showed that the environmental quality was either clean or almost clean. Pollutant enrichment analysis showed that the four sub-regions had similar pollution-causing metals to the background values of the soil element of the Liao River Plain, which were ranked according to their similarity. Source identification showed that all the elements were correlated. Ecological hazard analysis showed that the environmental risk index in the study area was less than zero, posing a low ecological risk. Ecological risk of the six elements was as follows: As > Cd > Hg > Cu > Pb > Zn.

Assessment of Pb, Cd and Hg soil contamination and its potential to cause cytotoxic and genotoxic effects in human cell lines (CaCo-2 and HaCaT).

Science.gov (United States)

Sljivic Husejnovic, Maida; Bergant, Martina; Jankovic, Sasa; Zizek, Suzana; Smajlovic, Aida; Softic, Adaleta; Music, Omer; Antonijevic, Biljana

2018-01-23

Soil contamination by heavy metals is a serious global environmental problem, especially for developing countries. A large number of industrial plants, which continually pollute the environment, characterize Tuzla Canton, Bosnia and Herzegovina. The aim of this study was to assess the level of soil pollution by heavy metals and to estimate cytotoxicity and genotoxicity of soil leachates from this area. Lead (Pb), cadmium (Cd) and mercury (Hg) were analyzed by ICP-AES and AAS. Soil contamination was assessed using contamination factor, degree of contamination, geoaccumulation index and pollution load index. To determine the connection of variables and understanding their origin in soils, principal component analysis (PCA) and cluster analysis (CA) were used. The results indicate that Cd and Hg originated from natural and anthropogenic activities, while Pb is of anthropogenic origin. For toxicity evaluation, CaCo-2 and HaCaT cells were used. PrestoBlue assay was used for cytotoxicity testing, and γH2A.X for genotoxicity evaluation. Concerning cytotoxicity, Cd and Hg had a positive correlation with cytotoxicity in HaCaT cells, but only Hg induced cytotoxicity in CaCo-2 cells. We also demonstrate that soil leachates contaminated by heavy metals can induce genotoxicity in both used cell lines. According to these results, combining bioassays with standard physicochemical analysis can be useful for evaluating environmental and health risks more accurately. These results are important for developing proper management strategies to decrease pollution. This is one of the first studies from this area and an important indication of soil quality in Southeast Europe.

Analysis of whole human blood for Pb, Cd, Hg, Se, and Mn by ICP-DRC-MS for biomonitoring and acute exposures.

Science.gov (United States)

Jones, Deanna R; Jarrett, Jeffery M; Tevis, Denise S; Franklin, Melanie; Mullinix, Neva J; Wallon, Kristen L; Derrick Quarles, C; Caldwell, Kathleen L; Jones, Robert L

2017-01-01

We improved our inductively coupled plasma mass spectrometry (ICP-MS) whole blood method [1] for determination of lead (Pb), cadmium (Cd), and mercury (Hg) by including manganese (Mn) and selenium (Se), and expanding the calibration range of all analytes. The method is validated on a PerkinElmer (PE) ELAN® DRC II ICP-MS (ICP-DRC-MS) and uses the Dynamic Reaction Cell (DRC) technology to attenuate interfering background ion signals via ion-molecule reactions. Methane gas (CH 4 ) eliminates background signal from 40 Ar 2 + to permit determination of 80 Se + , and oxygen gas (O 2 ) eliminates several polyatomic interferences (e.g. 40 Ar 15 N + , 54 Fe 1 H + ) on 55 Mn + . Hg sensitivity in DRC mode is a factor of two higher than vented mode when measured under the same DRC conditions as Mn due to collisional focusing of the ion beam. To compensate for the expanded method's longer analysis time (due to DRC mode pause delays), we implemented an SC4-FAST autosampler (ESI Scientific, Omaha, NE), which vacuum loads the sample onto a loop, to keep the sample-to-sample measurement time to less than 5min, allowing for preparation and analysis of 60 samples in an 8-h work shift. The longer analysis time also resulted in faster breakdown of the hydrocarbon oil in the interface roughing pump. The replacement of the standard roughing pump with a pump using a fluorinated lubricant, Fomblin®, extended the time between pump maintenance. We optimized the diluent and rinse solution components to reduce carryover from high concentration samples and prevent the formation of precipitates. We performed a robust calculation to determine the following limits of detection (LOD) in whole blood: 0.07µgdL -1 for Pb, 0.10µgL -1 for Cd, 0.28μgL -1 for Hg, 0.99µgL -1 for Mn, and 24.5µgL -1 for Se. Published by Elsevier B.V.

Collective oblate bands in Pb nuclei

Energy Technology Data Exchange (ETDEWEB)

Huebel, H; Baldsefen, G; Mehta, D [Bonn Univ. (Germany). Inst. fuer Strahlen- und Kernphysik; and others

1992-08-01

The coexistence of different nuclear shapes is a well established phenomenon in the Hg-Pb region, where spherical, oblate, prolate and superdeformed prolate shapes have been observed. In this work, the authors report on several new rotational bands in the normally spherical nuclei {sup 199-201}Pb. Similar structures were found previously in the lighter isotopes {sup 197,198}Pb. 11 refs., 1 tab., 3 figs.

Concentración de Hg, Pb, Cd, Cr y As en hígado de Carcharhinus limbatus (Carcharhiniformes: Carcharhinidae capturado en Veracruz, México

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Fernando Mendoza-Díaz

2013-06-01

Full Text Available La contaminación de los ecosistemas marinos y costeros por metales pesados en el Golfo de México es uno de los problemas que afectan a los recursos naturales del medio acuático. Los tiburones por situarse en niveles tróficos superiores de la red alimenticia acumulan y magnifican cantidades considerables de contaminantes. Por esta razón, el objetivo de este trabajo fue determinar la concentración de cuatro metales pesados (Hg, Cd, Pb y Cr y un metaloide (As en el tiburón punta negra (Carcharhinus limbatus por medio de espectrofotometría de absorción atómica con flama y generador de hidruros. Se muestrearon 19 hígados de tiburones capturados cerca de Tamiahua, Veracruz entre noviembre 2007 y marzo 2008, de los cuales 12 fueron machos adultos, una hembra adulta, tres machos jóvenes y tres hembras jóvenes. Las concentraciones máximas registradas para cada metal fueron: Hg=0.69mg/ kg, Cd=0.43mg/kg, As=27.37mg/kg, Cr=0.35mg/kg. El Pb no fue detectado, no al menos la cantidad mínima de detección requerida por el espectrofotómetro de absorción atómica (0.1mg/kg. Ninguna de las muestras analizadas rebasó los límites máximos permisibles por las leyes mexicanas y americanas.Concentration of Hg, Pb, Cd, Cr and As in liver Carcharhinus limbatus (Carcharhiniformes: Carcharhinidae captured in Veracruz, Mexico. Pollution by heavy metals in marine ecosystems in the Gulf of Mexico is one of the hardest conservation issues to solve. Sharks as top predators are bioindicators of the marine ecosystem health, since they tend to bioaccumulate and biomagnify contaminants; they also represent a food source for local consumption. Thus, the objective of this study was to study the possible presence of heavy metals and a metalloid in livers of Carcharhinus limbatus. For this, a total of 19 shark livers were taken from animals captured nearby Tamihua, Veracruz, Mexico from December 2007 to April 2008. 12 out of the 19 captured sharks were males, one was

Solar photocatalytic removal of Cu(II), Ni(II), Zn(II) and Pb(II): Speciation modeling of metal-citric acid complexes

International Nuclear Information System (INIS)

Kabra, Kavita; Chaudhary, Rubina; Sawhney, R.L.

2008-01-01

The present study is targeted on solar photocatalytic removal of metal ions from wastewater. Photoreductive deposition and dark adsorption of metal ions Cu(II), Ni(II), Pb(II) and Zn(II), using solar energy irradiated TiO 2 , has been investigated. Citric acid has been used as a hole scavenger. Modeling of metal species has been performed and speciation is used as a tool for discussing the photodeposition trends. Ninety-seven percent reductive deposition was obtained for copper. The deposition values of other metals were significantly low [nickel (36.4%), zinc (22.2%) and lead (41.4%)], indicating that the photocatalytic treatment process, using solar energy, was more suitable for wastewater containing Cu(II) ions. In absence of citric acid, the decreasing order deposition was Cu(II) > Ni(II) > Pb(II) > Zn(II), which proves the theoretical thermodynamic predictions about the metals

Concentrations, Distribution, and Ecological Risk Assessment of Heavy Metals in Daya Bay, China

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Huijuan Tang

2018-06-01

Full Text Available Surface sediment samples were collected from 19 sites throughout Daya Bay, China to study the concentrations, spatial distributions, potential ecological risk, and possible sources of heavy, including metals copper (Cu, zinc (Zn, arsenic (As, cadmium (Cd, nickel (Ni, lead (Pb, mercury (Hg, and chromium (Cr. The mean concentrations of the eight heavy metals were 24, 109, 6.5, 0.09, 35.3, 26.8, 0.07, and 109 µg g−1, respectively. The concentrations of most heavy metals were within range of those recorded in previous years. The spatial distribution pattern of most heavy metals were similar, with lowest values recorded along the southeast coast and the open sea area; the highest values were recorded in the northern Daya Bay, especially the northwest. Cu, Zn, As, Cd, Pb, and Hg were classified as Class I, and Ni and Cr were classified as Class II according to the Sediment Quality Guidelines (SQGs of China. The potential ecological risk (Eif indices of Cu, Zn, As, Pb, Ni, and Cr specify that these metals pose low risk to the ecosystem of the Bay, whereas Cd and Hg pose a very high risk in some sites. The geoaccumulation indices (Igeo of Cu, Zn, As, Ni, and Cr specify weak or no pollution in Daya Bay, whereas those of Pb, Cd, and Hg in some sites indicate moderate or even high pollution. Spatial distribution, carbon/nitrogen analysis, Pearson correlation, and principal components analysis indicated that Cu, Zn, As, Pb, Ni, Cr, total organic carbon (TOC, and total nitrogen (TN originated from the same sources. Ballast water or sewage from the cargo ships that park at the harbors or anchor in the Bay were the important sources for Cu, Zn, As, Pb, Ni, Cr, TOC, and TN. Other anthropogenic sources, such as agricultural runoff and aquaculture, might also be responsible, whereas Hg and Cd originated from other point sources.

Coulomb excitation of 206Hg at relativistic energies

Science.gov (United States)

Alexander, Tom

The region of the nuclear chart surrounding the doubly-magic nucleus 208Pb provides a key area to constrain and develop contemporary nuclear structure models. One aspect of particular interest is the transition strength of the first excited 2+ state in even-even nuclei; this work describes the measurement of this value for the case of 206Hg, where the Z=80 line meets the N=126 shell closure. The nuclei of interest were synthesized using relativistic-energy projectile fragmentation at the GSI facility in Germany. They were produced in the fragmentation of a primary 208Pb beam at an energy of 1 GeV per nucleon, and separated and identifed using the Fragment Separator. The secondary beams with an energy of 140 MeV per nucleon were Coulomb excited on a secondary target of 400 mg/cm. 2 gold. Gamma-rays were detected with the Advanced GAmma Tracking Array (AGATA). The precise scattering angle for Doppler-correction was determined with position information from the Lund-York-Cologne-CAlorimeter(LYCCA). Using the sophisticated tracking algorithm native to AGATA in conjunction with pulse-shape analysis, a precise Doppler-correction is performed on the gamma spectra, and using a complex n-dimensional analysis, the B(E2) value for 206Hg is extracted relative to the known value also measured in 206Pb. A total of 409 million 206Hg particles were measured, and a cross-section of 50 mb was determined for the 2+ state at 1068 keV. The measurement of the B(E2) transition strength was found to be 1.109 W.u. This result is compared to a number of theoretical calculations, including two Gogny forces, and a modified shell model parametrization and is found to be smaller than all calculated estimations, implying that the first excited 2. + state in . {206}Hg is uncollective in nature.

Multivariate statistical analysis of heavy metals in street dust of Baoji, NW China

International Nuclear Information System (INIS)

Lu Xinwei; Wang Lijun; Li, Loretta Y.; Lei Kai; Huang Li; Kang Dan

2010-01-01

The concentrations of Pb, Cu, Zn, Mn, Ni, Co and Cr in street dust samples from Baoji in north-west China were measured by wavelength dispersive X-ray fluorescence spectrometry, while As and Hg in street dust samples were determined by atomic fluorescence spectrometry. Principal component analysis and cluster analysis, coupled with correlation coefficient analysis, were used to analyze the data and to identify possible sources of these heavy metals. The results indicate that street dust in Baoji has elevated heavy metal concentrations, especially Hg, Pb, Zn and Cu, which are 16-77, 7-92, 6-26 and 4-12 times the background levels in Shaanxi soil, respectively. The mean heavy metal concentrations in street dust divided by the corresponding background values of Shaanxi soil decrease in the order of Hg > Pb > Zn > Cu > Cr > As > Ni > Co > Mn > V. Three main sources of these heavy metals were identified. As, V, Pb and Co originated from nature and traffic. Cu, Zn, Hg and Mn, especially the former two, mainly derive from industry sources, as well as traffic. Cr and Ni mainly originate from soil.

Heavy metal pollution and Pb isotopic tracing in the intertidal surface sediments of Quanzhou Bay, southeast coast of China

International Nuclear Information System (INIS)

Yu, Ruilian; Zhang, Weifang; Hu, Gongren; Lin, Chengqi; Yang, Qiuli

2016-01-01

Concentrations of 16 heavy metals and Pb isotopic ratios in the intertidal surface sediments of Quanzhou Bay were determined to study the pollution level of heavy metals and the sources of Pb. The results showed that most concentrations of Cd, Sn, Mn, Cu, Zn, Cr, Pb, Hg, Ni, Co, Cs, Fe and V were higher than the background values, while most concentrations of Ti, Sb and Sr were lower than the background values. The mean concentrations of Cu, Zn, Pb, Cr and Cd exceeded the first-grade criteria of Chinese marine sediment quality. The geo-accumulation indexes revealed that the sediments had been polluted by some heavy metals. The results of Pb isotopic tracing indicated that the total Pb in the sediments were mainly from parent material, industrial emission and vehicle exhaust with the mean contributions of 38.2%, 51.3% and 10.5%, respectively, calculated by a three-end-member model of Pb isotopic ratios. - Highlights: •Level of 16 heavy metals in intertidal surface sediments of Quanzhou Bay was studied. •The sediments had been polluted by some heavy metals including Pb. •Pb isotopic compositions in the sediments and the potential sources were determined. •A three-end member model was applied to estimate the contributions of Pb sources. •Industrial emission was the major anthropogenic Pb contributor in the sediments.

A flexible, high-performance magnetoelectric heterostructure of (001) oriented Pb(Zr0.52Ti0.48)O3 film grown on Ni foil

Science.gov (United States)

Palneedi, Haribabu; Yeo, Hong Goo; Hwang, Geon-Tae; Annapureddy, Venkateswarlu; Kim, Jong-Woo; Choi, Jong-Jin; Trolier-McKinstry, Susan; Ryu, Jungho

2017-09-01

In this study, a flexible magnetoelectric (ME) heterostructure of PZT/Ni was fabricated by depositing a (001) oriented Pb(Zr0.52Ti0.48)O3 (PZT) film on a thin, flexible Ni foil buffered with LaNiO3/HfO2. Excellent ferroelectric properties and large ME voltage coefficient of 3.2 V/cmṡOe were realized from the PZT/Ni heterostructure. The PZT/Ni composite's high performance was attributed to strong texturing of the PZT film, coupled with the compressive stress in the piezoelectric film. Besides, reduced substrate clamping in the PZT film due to the film on the foil structure and strong interfacial bonding in the PZT/LaNiO3/HfO2/Ni heterostructure could also have contributed to the high ME performance of PZT/Ni.

Electronic properties of liquid Hg-In alloys : Ab-initio molecular dynamics study

International Nuclear Information System (INIS)

Sharma, Nalini; Ahluwalia, P. K.; Thakur, Anil

2016-01-01

Ab-initio molecular dynamics simulations are performed to study the structural properties of liquid Hg-In alloys. The interatomic interactions are described by ab-initio pseudopotentials given by Troullier and Martins. Three liquid Hg-In alloys (Hg_1_0In_9_0, Hg_3_0In_7_0_,_. Hg_5_0In_5_0, Hg_7_0In_3_0, and Hg_9_0Pb_1_0) at 299 K are considered. The calculated results for liquid Hg (l-Hg) and lead (l-In) are also drawn. Along with the calculated results of considered five liquid alloys of Hg-In alloy. The results obtained from electronic properties namely total density of state and partial density of states help to find the local arrangement of Hg and In atoms and the presence of liquid state in the considered five alloys.

Total Contents and Sequential Extraction of Heavy Metals in Soils Irrigated with Wastewater, Akaki, Ethiopia

Science.gov (United States)

Fitamo, Daniel; Itana, Fisseha; Olsson, Mats

2007-02-01

The Akaki River, laden with untreated wastes from domestic, industrial, and commercial sources, serves as a source of water for irrigating vegetable farms. The purpose of this study is to identify the impact of waste-water irrigation on the level of heavy metals and to predict their potential mobility and bioavailability. Zn and V had the highest, whereas Hg the lowest, concentrations observed in the soils. The average contents of As, Co, Cr, Cu, Ni, Zn, V, and Hg of both soils; and Pb and Se from Fluvisol surpassed the mean + 2 SD of the corresponding levels reported for their uncontaminated counterparts. Apparently, irrigation with waste water for the last few decades has contributed to the observed higher concentrations of the above elements in the study soils (Vertisol and Fluvisol) when compared to uncontaminated Vertisol and Fluvisol. On the other hand, Vertisol accommodated comparatively higher average levels of Cr, Cu, Ni, Zn, etc V, and Cd, whereas high contents of Pb and Se were observed in Fluvisol. Alternatively, comparable levels of Co and Hg were found in either soil. Except for Ni, Cr, and Cd in contaminated Vertisol, heavy metals in the soils were not significantly affected by the depth (0-20 and 30-50 cm). When the same element from the two soils was compared, the levels of Cr, Cu, Ni, Pb, Se, Zn, V, Cd at 0-20 cm; and Cr, Ni, Cu, Cd, and Zn at 30-50 cm were significantly different. Organic carbon (in both soils), CEC (Fluvisol), and clay (Vertisol) exhibited significant positive correspondences with the total heavy metal levels. Conversely, Se and Hg contents revealed perceptible associations with carbonate and pH. The exchangeable fraction was dominated by Hg and Cd, whereas the carbonate fraction was abounded with Cd, Pb, and Co. conversely, V and Pb displayed strong affinity to reducible fraction, where as Cr, Cu, Zn, and Ni dominated the oxidizable fraction. Cr, Hg, Se, and Zn (in both soils) showed preference to the residual fraction

As, Cd, Cr, Ni and Pb pressurized liquid extraction with acetic acid from marine sediment and soil samples

International Nuclear Information System (INIS)

Moreda-Pineiro, Jorge; Alonso-Rodriguez, Elia; Lopez-Mahia, Purificacion; Muniategui-Lorenzo, Soledad; Prada-Rodriguez, Dario; Moreda-Pineiro, Antonio; Bermejo-Barrera, Adela; Bermejo-Barrera, Pilar

2006-01-01

Rapid leaching procedures by Pressurized Liquid Extraction (PLE) have been developed for As, Cd, Cr, Ni and Pb leaching from environmental matrices (marine sediment and soil samples). The Pressurized Liquid Extraction is completed after 16 min. The released elements by acetic acid Pressurized Liquid Extraction have been evaluated by inductively coupled plasma-optical emission spectrometry. The optimum multi-element leaching conditions when using 5.0 ml stainless steel extraction cells, were: acetic acid concentration 8.0 M, extraction temperature 100 deg. C, pressure 1500 psi, static time 5 min, flush solvent 60%, two extraction steps and 0.50 g of diatomaceous earth as dispersing agent (diatomaceous earth mass/sample mass ratio of 2). Results have showed that high acetic acid concentrations and high extraction temperatures increase the metal leaching efficiency. Limits of detection (between 0.12 and 0.5 μg g -1 ) and repeatability of the over-all procedure (around 6.0%) were assessed. Finally, accuracy was studied by analyzing PACS-2 (marine sediment), GBW-07409 (soil), IRANT-12-1-07 (cambisol soil) and IRANT-12-1-08 (luvisol soil) certified reference materials (CRMs). These certified reference materials offer certified concentrations ranges between 2.9 and 26.2 μg g -1 for As, from 0.068 to 2.85 μg g -1 for Cd, between 26.4 and 90.7 μg g -1 for Cr, from 9.3 to 40.0 μg g -1 for Ni and between 16.3 and 183.0 μg g -1 for Pb. Recoveries after analysis were between 95.7 and 105.1% for As, 96.2% for Cd, 95.2 and 100.6% for Cr, 95.7 and 103% for Ni and 94.2 and 105.5% for Pb

Valence States Modulation Strategy for Picomole Level Assay of Hg2+ in Drinking and Environmental Water by Directional Self-Assembly of Gold Nanorods.

Science.gov (United States)

Chen, Lu; Lu, Linlin; Wang, Sufan; Xia, Yunsheng

2017-06-23

In this study, we present a valence states modulation strategy for picomole level assay of Hg 2+ using directional self-assembly of gold nanorods (AuNRs) as signal readout. Hg 2+ ions are first controllably reduced to Hg + ions by appropriate ascorbic acid, and the reduced Hg + ions react with the tips of the preadded AuNRs and form gold amalgam. Such Hg + decorated AuNRs then end-to-end self-assemble into one-dimensional architectures by the bridging effects of lysine based on the high affinity of NH 2 -Hg + interactions. Correspondingly, the AuNRs' longitudinal surface plasmon resonance is gradually reduced and a new broad band appears at 900-1100 nm region simultaneously. The resulting distinctly ratiometric signal output is not only favorable for Hg 2+ ions detection but competent for their quantification. Under optimal conditions, the linear range is 22.8 pM to 11.4 nM, and the detection limit is as low as 8.7 pM. Various transition/heavy metal ions, such as Pb 2+ , Ti 2+ , Co 2+ , Fe 3+ , Mn 2+ , Ba 2+ , Fe 2+ , Ni 2+ , Al 3+ , Cu 2+ , Ag + , and Au 3+ , do not interfere with the assay. Because of ultrahigh sensitivity and excellent selectivity, the proposed system can be employed for assaying ultratrace of Hg 2+ containing in drinking and commonly environmental water samples, which is difficult to be achieved by conventional colorimetric systems. These results indicate that the present platform possesses specific advantages and potential applications in the assay of ultratrace amounts of Hg 2+ ions.

Efficient CH3NH3PbI3 perovskite/fullerene planar heterojunction hybrid solar cells with oxidized Ni/Au/Cu transparent electrode

Science.gov (United States)

Lai, Wei-Chih; Lin, Kun-Wei; Guo, Tzung-Fang; Chen, Peter; Liao, Yuan-Yu

2018-02-01

We demonstrated the performance of inverted CH3NH3PbI3 perovskite-based solar cells (SCs) with a thermally oxidized nickel/gold/copper (Ni/Au/Cu) trilayer transparent electrode. Oxidized Ni/Au/Cu is a high transparent layer and has less resistance than the oxidized Ni/Au layer. Like the oxidized Ni/Au layer, oxidized Ni and Cu in oxidized Ni/Au/Cu could perform as a hole transport layer of the perovskite-based SCs. It leads to improved perovskite SC performance on an open circuit voltage of 1.01 V, a short circuit current density of 14.36 mA/cm2, a fill factor of 76.7%, and a power conversion efficiency (η%) of 11.1%. The η% of perovskite SCs with oxidized Ni (10 nm)/Au (6 nm)/Cu (1 nm) improved by approximately 10% compared with that of perovskite SCs with oxidized Ni/Au.

Spectroscopic features of Ni(2+) ion in PbO-Bi2O3-SiO2 glass system.

Science.gov (United States)

Suresh, B; Srinivasa Reddy, M; Siva Sesha Reddy, A; Gandhi, Y; Ravi Kumar, V; Veeraiah, N

2015-04-15

Glasses of the composition (30-x)PbO-5Bi2O3-65SiO2: xNiO (with x ranging from 0 to 1.0 mol%) were synthesized. A variety of spectroscopic studies, viz., IR, Raman optical absorption and luminescence properties of these glasses have been carried out as a function of NiO concentration. The analysis of results of all these studies has indicated that the nickel ions occupy both octahedral and tetrahedral positions. However, with the increase of NiO concentration the octahedral occupancy of Ni(2+) ions prevailed over the tetrahedral ions. The luminescence spectra of these glasses have exhibited a broad NIR emission band in region 1100-1500 nm. This band is identified as being due to (3)T2(3F)→(3)A2(3F) octahedral transition of Ni(2+) ions. The luminescence efficiency and cross section have been found to be the highest for the glass containing the highest concentration of NiO. The reasons for such high luminescence efficiency have been discussed in the light of structural variations taking place in the host glass network. Copyright © 2015 Elsevier B.V. All rights reserved.

Exploring the Effects of the Pb2+ Substitution in MAPbI3 on the Photovoltaic Performance of the Hybrid Perovskite Solar Cells.

Science.gov (United States)

Frolova, Lyubov A; Anokhin, Denis V; Gerasimov, Kirill L; Dremova, Nadezhda N; Troshin, Pavel A

2016-11-03

Here we report a systematic study of the Pb 2+ substitution in the hybrid iodoplumbate MAPbI 3 with a series of elements affecting optoelectronic, structural, and morphological properties of the system. It has been shown that even partial replacement of lead with Cd 2+ , Zn 2+ , Fe 2+ , Ni 2+ , Co 2+ , In 3+ , Bi 3+ , Sn 4+ , and Ti 4+ results in a significant deterioration of the photovoltaic characteristics. On the contrary, Hg-containing hybrid MAPb 1-x Hg x I 3 salts demonstrated a considerably improved solar cell performance at optimal mercury loading. This result opens up additional dimension in the compositional engineering of the complex lead halides for designing novel photoactive materials with advanced optoelectronic and photovoltaic properties.

New Mn(II, Ni(II, Cd(II, Pb(II complexes with 2-methylbenzimidazole and other ligands. Synthesis, spectroscopic characterization, crystal structure, magnetic susceptibility and biological activity studies

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Shayma A. Shaker

2016-11-01

Full Text Available Synthesis and characterization of Mn(II, Ni(II, Cd(II and Pb(II mixed ligand complexes of 2-methylbenzimidazole with other ligands have been reported. The structure of the ligands and their complexes was investigated using elemental analysis, IR, UV–Vis, (1H, 13C NMR spectroscopy, molar conductivity and magnetic susceptibility measurements. In all the studies of complexes, the 2-methylbenzimidazole behaves as a neutral monodentate ligand which is coordinated with the metal ions through the N atom. While benzotriazole behaves as a neutral bidentate ligand which is coordinated with the Ni(II ion through the two N atoms. Moreover, the N-acetylglycine behaves as a bidentate ligand which is coordinated with the Mn(II, Ni(II and Pb(II ions through the N atom and the terminal carboxyl oxygen atom. The magnetic and spectral data indicate the tetrahedral geometry for Mn(II complex, irregular tetrahedral geometry for Pb(II complex and octahedral geometry for Ni(II complex. The X-ray single crystal diffraction method was used to confirm a centrosymmetric dinuclear Cd(II complex as each two metal ions are linked by a pair of thiocyanate N = S bridge. Two 2-methylbenzimidazole N-atom donors and one terminal thiocyanate N atom complete a highly distorted square pyramid geometry around the Cd atom. Besides, different cell types were used to determine the inhibitory effect of Mn(II, Ni(II, Cd(II and Pb(II complexes on cell growth using MTT assay. Cd(II complex showed cytotoxic effect on various types of cancer cell lines with different EC50 values.

Susceptibility of Arcobacter butzleri to heavy metals Sensibilidade de Arcobacter butzleri a metais pesados

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Laura Otth

2005-09-01

Full Text Available The susceptibility of 50 strains of Arcobacter butzleri isolated from chicken liver [12], mussels [18], river water [6] and bovine [5], duck [2] and pelicans [7] feces to mercury (Hg, chromium (Cr, silver (Ag, nickel (Ni, cobalt (Co, iron (Fe, manganese (Mn, molybdenum (Mo and lead (Pb was determined.All the strains were resistant to Mo, Mn, Ni, Co, Pb and Fe and susceptible to Hg, Ag and Cr. MIC values showed high variability, indicating a non homogeneous behavior among the strains.Arcobacter butzleri é um bacilo Gram negativo de caráter zoonótico, pertencente à Família Campylobacteraceae, que tem sido associado a diarréia e septicemia no ser humano. A susceptibilidade de 50 amostras de A. butzleri isoladas de fígados de frango [12], mariscos [18], água de rio [6] e fezes de bovinos [5], patos [2] e pelicanos [7] aos metais pesados mercúrio (Hg, cromo (Cr, prata (Ag, níquel (Ni, cobalto Co, ferro (Fe, manganês (Mn, molibdênio (Mo e chumbo (Pb foi determinada.Todas as amostras foram resistentes a Mo, Mn, Ni, Co, Pb e Fe, sendo susceptíveis a Hg, Ag e Cr. Os valores das CIM apresentaram alta variabilidade indicando um comportamento não homogêneo entre as amostras.

Atomic substitution effects on the structural and vibrational properties of Ni{sub x}Pb{sub 1-x}TiO{sub 3}: X-ray diffraction and Raman scattering investigations

Energy Technology Data Exchange (ETDEWEB)

Costa, R. C. da [Universidade Federal de São Carlos, Departamento de Física, São Carlos-SP, 13565-905 (Brazil); Universidade Federal de Campina Grande, Pombal-PB, 58840-000 (Brazil); Toledo, T. A. de; Pizani, P. S., E-mail: pizani@df.ufscar.br [Universidade Federal de São Carlos, Departamento de Física, São Carlos-SP, 13565-905 (Brazil); Espinosa, J. W. M. [Universidade Federal de Goiás, Engenharia de Produção, Catalão-GO, 75704-020 (Brazil)

2015-07-15

The effects of the atomic substitution of Pb by Ni in the PbTiO{sub 3} ferroelectric perovskite on the vibrational and structural properties was studied using x-ray diffraction and Raman scattering. It was observed that for Ni concentrations between 0.0 and 0.4, there is the formation of a solid solution with reduction of the Raman wavenumber of the E(TO1) soft mode and the tetragonallity factor, which influence directly the temperature of the tetragonal ferroelectric to cubic paraelectric phase transition, the Curie temperature. For concentrations greater than 0.4, it is observed the formation of a PbTiO{sub 3} and NiTiO{sub 3} composite, denounced by the recovering of the both, tetragonallity factor and the E(TO1) soft mode wavenumber. The values of the Curie temperatures were estimated by the Raman scattering measurements for temperatures ranging from 300 to 950 K.

Enhanced Hg{sup 2+} removal and Hg{sup 0} re-emission control from wet fuel gas desulfurization liquors with additives

Energy Technology Data Exchange (ETDEWEB)

Tingmei Tang; Jiang Xu; Rongjie Lu; Jingjing Wo; Xinhua Xu [Zhejiang University, Hangzhou (China). Department of Environmental Engineering

2010-12-15

Secondary atmospheric pollutions may result from wet flue gas desulfurization (FGD) systems caused by the reduction of Hg{sup 2+} to Hg{sup 0}. The present study employed three agents: Na{sub 2}S, 2,4,6-trimercaptotiazine, trisodium salt nonahydrate (TMT) and sodium dithiocarbamate (DTCR) to precipitate aqueous Hg{sup 2+} in simulated desulfurization solutions. The effects of the precipitator's dosing quantity, the initial pH value, the reaction temperature, the concentrations of Cl{sup -} and other metal ions (e.g. Cu{sup 2+} and Pb{sup 2+}) on Hg{sup 2+} removal were studied. A linear relationship was observed between Hg{sup 2+} removal efficiency and the increasing precipitator's doses along with initial pH. The addition of chloride and metal ions impaired the Hg{sup 2+} removal from solutions due to the complexation of Cl{sup -} and Hg{sup 2+} as well as the chelating competition between Hg{sup 2+} and other metal ions. Based on a comprehensive comparison of the treatment effects, DTCR was found to be the most effective precipitating agent. Moreover, all the precipitating agents were potent enough to inhibit Hg{sup 2+} reduction as well as Hg{sup 0} re-emission from FGD liquors. More than 90% Hg{sup 2+} was captured by precipitating agents while Hg{sup 2+} reduction efficiency decreased from 54% to just less than 3%. The additives could efficiently control the secondary Hg{sup 0} pollution from FGD liquors. 21 refs., 6 figs.

Direct lead isotope analysis in Hg-rich sulfides by LA-MC-ICP-MS with a gas exchange device and matrix-matched calibration

Energy Technology Data Exchange (ETDEWEB)

Zhang, Wen [State Key Laboratory of Geological Processes and Mineral Resources, Faculty of Earth Sciences, China University of Geosciences, Wuhan, 430074 (China); Hu, Zhaochu, E-mail: zchu@vip.sina.com [State Key Laboratory of Geological Processes and Mineral Resources, Faculty of Earth Sciences, China University of Geosciences, Wuhan, 430074 (China); Günther, Detlef, E-mail: guenther@inorg.chem.ethz.ch [ETH Zurich, Laboratory for Inorganic Chemistry, CH-8093, Zurich (Switzerland); Liu, Yongsheng; Ling, Wenli; Zong, Keqing; Chen, Haihong; Gao, Shan [State Key Laboratory of Geological Processes and Mineral Resources, Faculty of Earth Sciences, China University of Geosciences, Wuhan, 430074 (China)

2016-12-15

In situ Pb isotope data of sulfide samples measured by LA-MC-ICP-MS provide valuable geochemical information for studies of the origin and evolution of ore deposits. However, the severe isobaric interference of {sup 204}Hg on {sup 204}Pb and the lack of matrix-matched sulfide reference materials limit the precision of Pb isotopic analyses for Hg-rich sulfides. In this study, we observe that Hg forms vapor and can be completely removed from sample aerosol particles produced by laser ablation using a gas exchange device. Additionally, this device does not influence the signal intensities of Pb isotopes. The within-run precision, the external reproducibility and the analytical accuracy are significantly improved for the Hg-rich sulfide samples using this mercury-vapor-removing device. Matrix effects are observed when using silicate glass reference materials as the external standards to assess the relationship of mass fractionation factors between Tl and Pb in sulfide samples, resulting in a maximum deviation of ∼0.20% for {sup 20x}Pb/{sup 204}Pb. Matrix-matched reference materials are therefore required for the highly precise and accurate Pb isotope analyses of sulfide samples. We investigated two sulfide samples, MASS-1 (the Unites States Geological Survey reference materials) and Sph-HYLM (a natural sphalerite), as potential candidates. Repeated analyses of the two proposed sulfide reference materials by LA-MC-ICP-MS yield good external reproducibility of <0.04% (RSD, k = 2) for {sup 20x}Pb/{sup 206}Pb and <0.06% (RSD, k = 2) for {sup 20x}Pb/{sup 204}Pb with the exception of {sup 20x}Pb/{sup 204}Pb in MASS-1, which provided an external reproducibility of 0.24% (RSD, k = 2). Because the concentration of Pb in MASS-1 (76 μg g{sup −1}) is ∼5.2 times lower than that in Sph-HYLM (394 ± 264 μg g{sup −1}). The in situ analytical results of MASS-1 and Sph-HYLM are consistent with the values obtained by solution MC-ICP-MS, demonstrating the reliability

Generation of covariance files for the isotopes of Cr, Fe, Ni, Cu, and Pb in ENDF/B-VI

International Nuclear Information System (INIS)

Hetrick, D.M.; Larson, D.C.; Fu, C.Y.

1991-02-01

The considerations that governed the development of the uncertainty files for the isotopes of Cr, Fe, Ni, Cu, and Pb in ENDF/B-VI are summarized. Four different approaches were used in providing the covariance information. Some examples are given which show the standard deviations as a function of incident energy and the corresponding correlation matrices. 11 refs., 5 tabs

Uptake of Heavy Metal Residues from Sewerage Sludge in the Milk of Goat and Cattle during Summer Season

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Bilal Aslam, Ijaz Javed*, Faqir Hussain Khan and Zia-ur-Rahman

2011-01-01

Full Text Available Uptake of different heavy metal residues including cadmium (Cd, chromium (Cr, nickel (Ni, led (Pb, arsenic (As, and mercury (Hg were determined in goat and cattle milk collected from two areas, each consisted of three sites. Area 1 was selected in the North-East and Area 2 in the North-West of Faisalabad city along the main sewerage drains. Levels of Cd, Cr, Ni, Pb, As and Hg in the milk of goat and cattle were higher than the most reported values in the literature. The levels of heavy metal residues in the milk of cattle from Area 1 were higher than those present in cattle milk from Area 2. However, in case of goat milk the residual values from Area 1 and Area 2 were non-significantly different. It was concluded that the levels of Cd, Cr, Ni, Pb, As and Hg in the milk of goat and cattle were higher than reported values in the literature.

The effect of Fe, Mn, Ni and Pb Load on Soil and its enrichment factor ratios in different soil grain size fractions as an Indicator for soil pollution

International Nuclear Information System (INIS)

Rabie, F.H.; Abdel-Sabour, M.F.

2000-01-01

An industrial area north of greater Cairo was selected to investigate the impact of intensive industrial activities on soil characteristics and Fe, Mn, Ni and Pb total content. The studied area was divided to six sectors according to its source of irrigation water and/or probability of pollution. Sixteen soil profiles were dug and soil samples were taken, air dried, fractionated to different grain size fractions, then total heavy metals (Fe, Mn, Ni and Pb) were determined using ICP technique. The enrichment factor for each metal for each soil fraction/soil layer was estimated and discussed. The highest EF ratios in the clay fraction was mainly with Pb which indicated the industrial impact on the soil. In case of sand fraction, Mn was the highest always compared to other studied metals. Concerning silt fraction, a varied accumulation of Fe, Mn, and Pb was observed with soil depth and different soil profiles

Tsygankoite, Mn8Tl8Hg2(Sb21Pb2TlΣ24S48, a New Sulfosalt from the Vorontsovskoe Gold Deposit, Northern Urals, Russia

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Anatoly V. Kasatkin

2018-05-01

Full Text Available Tsygankoite, ideally Mn8Tl8Hg2(Sb21Pb2TlΣ24S48, is a new sulfosalt discovered at the Vorontsovskoe gold deposit, Northern Urals, Russia. It occurs as lath-like elongated crystals up to 0.2 mm embedded in calcite–dolomite–clinochlore matrix. The associated minerals also include aktashite, alabandite, arsenopyrite, barite, cinnabar, fluorapatite, orpiment, pyrite, realgar, routhierite, sphalerite, tilasite, and titanite. The new mineral is non-fluorescent, black, and opaque with a metallic lustre and black streak. It is brittle with an uneven fracture and no obvious parting and cleavage. Its Vickers hardness (VHN10 is 144 kg/mm2 (range 131–167 kg/mm2 and its calculated density is 5.450 g cm. In reflected light, tsygankoite is white; between crossed polars it is dark grey to black. It is strongly anisotropic: rotation tints vary from light grey to dark grey to black. Pleochroism and internal reflections are not observed. The chemical composition of tsygankoite (wt %, electron-microprobe data is: Mn 6.29, Hg 5.42, Tl 26.05, Pb 5.84, As 3.39, Sb 30.89, S 21.87, total 99.75. The empirical formula, calculated on the basis of 90 atoms pfu, is: Mn8.06Tl8.00Hg1.90(Sb17.87As3.19Pb1.99Tl0.97Σ24.02S48.03. Tsygankoite is monoclinic, space group C2/m, a = 21.362(4 Å, b = 3.8579(10 Å, c = 27.135(4 Å, β = 106.944(14°, V = 2139.19(17 Å3 and Z = 1. The five strongest diffraction peaks from X-ray powder pattern (listed as (d,Å(I(hkl are: 3.587(100(112, 3.353(70(−114, 3.204(88(405, 2.841(72(−513, and 2.786(99(−514. The crystal structure of tsygankoite was refined from single-crystal X-ray diffraction data to R = 0.0607 and consists of an alternation of two thick layer-like arrays, one based on PbS-archetype and the second on SnS-archetype. Tsygankoite has been approved by the IMA-CNMNC under the number 2017-088. It is named for Mikhail V. Tsyganko, a mineral collector from Severouralsk, Northern Urals, Russia, who collected the samples where the

The Effect of Oxygen Flow on the Transition Temperature of Hg0.75Pb0.25Sr2-yBayCa2Cu3O8+ δ Superconductors

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Jasim, Kareem A.; Al-Khafaji, Raghad S.

2018-05-01

In this paper, there are three different high temperature superconductors which are Hg0.75Pb0.25Sr2-y BayCa2Cu3O8+δ with deferent weight fractions y = 0.10, 0.20 and 0.25 that have been prepared successfully by solid state reaction and the samples have been equipped with/without O2 flow. The optimum calcinations is 1073 K and the sintering process that has been achieved within 1128-1133 K. Transition temperature Tc has been found by using four probe technique through electrical resistivity measurements. The greatest Tc that has been found for Hg0.75Pb0.25Sr1.75 Ba0.25Ca2Cu3O8.31 is 115 oK. Oxygen content (O2) flow exhibits high-phased superconductors that is similar to the samples prepared without O2. Investigation of X-ray diffraction (XRD) is revealed (tetragonal structure) by the c-axis lattice parameter increasing of the samples substituted with Ba. It has been established, from the calculated results, that the Ba variation concentrations of all samples products a modification in the density (ρm), (c/a) and volume fraction (VPh(2223)).

Anthropogenic impacts in North Poland over the last 1300 years - A record of Pb, Zn, Cu, Ni and S in an ombrotrophic peat bog

International Nuclear Information System (INIS)

De Vleeschouwer, Francois; Fagel, Nathalie; Cheburkin, Andriy; Pazdur, Anna; Sikorski, Jaroslaw; Mattielli, Nadine; Renson, Virginie; Fialkiewicz, Barbara; Piotrowska, Natalia; Le Roux, Gael

2009-01-01

Lead pollution history over Northern Poland was reconstructed for the last ca. 1300 years using the elemental and Pb isotope geochemistry of a dated Polish peat bog. The data show that Polish Pb-Zn ores and coal were the main sources of Pb, other heavy metals and S over Northern Poland up until the industrial revolution. After review of the potential mobility of each element, most of the historical interpretation was based on Pb and Pb isotopes, the other chemical elements (Zn, Cu, Ni, S) being considered secondary indicators of pollution. During the last century, leaded gasoline also contributed to anthropogenic Pb pollution over Poland. Coal and Pb-Zn ores, however, remained important sources of pollution in Eastern European countries during the last 50 years, as demonstrated by a high 206 Pb/ 207 Pb ratio (1.153) relative to that of Western Europe (ca. 1.10). The Pb data for the last century were also in good agreement with modelled Pb inventories over Poland and the Baltic region.

Final report of the key comparison CCQM-K106: Pb, As and Hg measurements in cosmetic (cream)

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Wang, Jun; Wang, Qian; Yamani, Randa Nasr Ahmed; Shehata, Adel B.; Jacimovic, Radojko; Pavlin, Majda; Horvat, Milena; Tsoi, Y. P.; Tsang, C. K.; Shin, Richard; Chailap, Benjamat; Yafa, Charun; Caciano de Sena, Rodrigo; de Almeida, Marcelo; Yim, Yong-Hyeon; Lee, Kyoung-Seok; Heun Kim, Sook; Konopelko, Leonid; Ari, Betül; Tokman, Nilgün; Rienitz, Olaf; Jaehrling, Reinhard; Pape, Carola

2015-01-01

Cosmetics are used in practically all walks of life as a means of improving skin and beautifying complexion. In recent years, more and more attention has been paid to the cosmetic safety. In response to the cosmetic safety issue, the accurate measurement of the heavy metals in cosmetics is, therefore, particularly important. NMIs from different countries should establish their chemical metrology traceability system in this area, which includes both measurement methods research and certain CRMs development. It should be noted that because the matrix of many cosmetics is complex and the contents of the heavy metals are relatively low, it still is a challenging task to measure the analytes with high accuracy and precision. CCQM-K106 followed up CCQM pilot study 'CCQM-P128: Pb, As measurements in cosmetic (cream)' coordinated by the National Institute of Metrology, China (NIM) in 2009. The cream was selected as the testing material, which is widely used as a daily skin care worldwide. This is the first CCQM key comparison regarding the measurement of toxic metal elements with the cosmetic matrix, which includes pure water, liquid paraffin, silicone oil, synthetic squalane, hyaluronic acid, glycerin, propylene glycol, allantoin, preservative and so on. The aim of the CCQM-K106 is to demonstrate the capability of participating NMIs and designated institutes in measuring the contents of poisonous elements, including lead, arsenic and mercury in a cosmetic sample (cream), and support CMC claims relating to inorganic elements in cosmetic materials and similar chemical industry products. The cream matrix sample was prepared under the guidance of professional technicians. The formula of the cream was carefully chosen to match with a real cosmetic. The homogeneity and stability level of Pb, As and Hg in the cream sample were fit for the objective of the comparison. Each participant received two numbered bottles containing about 5g samples in each bottle. The instruction

Concentración de Hg, Pb, Cd, Cr y As en hígado de Carcharhinus limbatus (Carcharhiniformes: Carcharhinidae capturado en Veracruz, México

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Fernando Mendoza-Díaz

2013-06-01

Full Text Available La contaminación de los ecosistemas marinos y costeros por metales pesados en el Golfo de México es uno de los problemas que afectan a los recursos naturales del medio acuático. Los tiburones por situarse en niveles tróficos superiores de la red alimenticia acumulan y magnifican cantidades considerables de contaminantes. Por esta razón, el objetivo de este trabajo fue determinar la concentración de cuatro metales pesados (Hg, Cd, Pb y Cr y un metaloide (As en el tiburón punta negra (Carcharhinus limbatus por medio de espectrofotometría de absorción atómica con flama y generador de hidruros. Se muestrearon 19 hígados de tiburones capturados cerca de Tamiahua, Veracruz entre noviembre 2007 y marzo 2008, de los cuales 12 fueron machos adultos, una hembra adulta, tres machos jóvenes y tres hembras jóvenes. Las concentraciones máximas registradas para cada metal fueron: Hg=0.69mg/ kg, Cd=0.43mg/kg, As=27.37mg/kg, Cr=0.35mg/kg. El Pb no fue detectado, no al menos la cantidad mínima de detección requerida por el espectrofotómetro de absorción atómica (0.1mg/kg. Ninguna de las muestras analizadas rebasó los límites máximos permisibles por las leyes mexicanas y americanas.

Evaluation of Cd, Cr, Cu, Ni, and Pb in selected cosmetic products from Jordanian, Sudanese, and Syrian markets.

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Massadeh, A M; El-Khateeb, M Y; Ibrahim, S M

2017-08-01

There is no sufficient data that evaluate heavy metal content in cosmetic products in Jordan as well as Sudan and Syria. This study aims to assess metal levels which include Cadmium (Cd), Chromium (Cr), Copper (Cu), Nickel (Ni), and Lead (Pb) in cosmetic products. These elements have draft limits because they are identified as potential impurities and are known to be toxic. This study aims to provide information to the population that may be beneficial to public health. Samples were collected from different brands obtained from markets in Jordan, Sudan, and Syria. Some of the selected cosmetic products were eyeliner, eye pencil, mascara, lipstick, powder, face cream, body cream, sun block, Vaseline, and the traditional eye cosmetic (kohl). The heavy metal content in these samples were determined by atomic absorption spectrometry (AAS). Based on analysis of variance analysis, a significant difference in heavy metal levels was found for samples obtained from Jordanian and Sudanese markets. The acid digestion method used in this study was based on procedures recommended by Nnorom et al. with some modifications as follows. (i) A weight of 2.0 g of cosmetic sample was dissolved in a mixture of 6 mL of high quality concentrated 69% nitric acid (HNO 3 ; Merck, Darmstadt, Germany) and 4 mL of concentrated 37% hydrochloric acid (Scharlau, Spain) in a porcelain crucible and heated on a hotplate to near dryness. (ii) An aliquot of 15 mL HNO 3 (1.00 M) was added to the digested sample and filtered through a Whatman No. 40 filter paper. (iii) The digested sample was transferred quantitatively into a 25 mL volumetric flask and then diluted with deionized water. (iv) Each digested sample was evaporated at 70 °C to about 1 mL and transferred into a polyethylene flask and diluted with 25 mL deionized water. (v) Blank was treated in the same procedure. In Jordan the concentration ranges of heavy metals in the collected samples were: Cd (0.03-0.10 μg/g), Cr (0.0-1.00�

Heavy metal pollution in soil associated with a large-scale cyanidation gold mining region in southeast of Jilin, China.

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Chen, Mo; Lu, Wenxi; Hou, Zeyu; Zhang, Yu; Jiang, Xue; Wu, Jichun

2017-01-01

Different gold mining and smelting processes can lead to distinctive heavy metal contamination patterns and results. This work examined heavy metal pollution from a large-scale cyanidation gold mining operation, which is distinguished from artisanal and small-scale amalgamation gold mining, in Jilin Province, China. A total of 20 samples including one background sample were collected from the surface of the mining area and the tailings pond in June 2013. These samples were analyzed for heavy metal concentrations and degree of pollution as well as sources of Cr, Cu, Zn, Pb, Ni, Cd, As, and Hg. The mean concentrations of Pb, Hg, and Cu (819.67, 0.12, and 46.92 mg kg -1 , respectively) in soil samples from the gold mine area exceeded local background values. The mean Hg content was less than the first-class standard of the Environmental Quality for Soils, which suggested that the cyanidation method is helpful for reducing Hg pollution. The geochemical accumulation index and enrichment factor results indicated clear signs that enrichment was present for Pb, Cu, and Hg, with the presence of serious Pb pollution and moderate presence to none of Hg and Cu pollution. Multivariate statistical analysis showed that there were three metal sources: (1) Pb, Cd, Cu, and As came from anthropogenic sources; (2) Cr and Zn were naturally occurring; whereas (3) Hg and Ni had a mix of anthropogenic and natural sources. Moreover, the tailings dam plays an important role in intercepting the tailings. Furthermore, the potential ecological risk assessment results showed that the study area poses a potentially strong risk to the ecological health. Furthermore, Pb and Hg (due to high concentration and high toxicity, respectively) are major pollutants on the risk index, and both Pb and Hg pollution should be of great concern at the Haigou gold mines in Jilin, China.

Experimental investigation of neutron generation in thick target blocks of Pb, Hg and W with 0.4 to 2.5 GeV proton beams

International Nuclear Information System (INIS)

Jahnke, U.; Enke, M.; Filges, D.

2002-01-01

Detailed experimental neutron data relevant to the design of the target station of neutron spallation sources have been gathered by the NESSI-collaboration at the COSY accelerator in FZ Juelich. Numerous neutron multiplicity distributions and reaction probabilities have been measured for 0.4 to 2.5 GeV protons bombarding highly segmented target blocks from Pb, Hg and W of up to 35 cm in length and 15 cm in diameter with the intention to provide a comprehensive data base for the improvement and validation of existing reaction simulation codes. (author)

[Concentration of Hg, Pb, Cd, Cr and As in liver Carcharhinus limbatus (Carcharhiniformes: Carcharhinidae) captured in Veracruz, Mexico].

Science.gov (United States)

Mendoza-Díaz, Fernando; Serrano, Arturo; Cuervo-López, Liliana; López-Jiménez, Alejandra; Galindo, José A; Basañez-Muñoz, Agustin

2013-06-01

Pollution by heavy metals in marine ecosystems in the Gulf of Mexico is one of the hardest conservation issues to solve. Sharks as top predators are bioindicators of the marine ecosystem health, since they tend to bioaccumulate and biomagnify contaminants; they also represent a food source for local consumption. Thus, the objective of this study was to study the possible presence of heavy metals and a metalloid in livers of Carcharhinus limbatus. For this, a total of 19 shark livers were taken from animals captured nearby Tamihua, Veracruz, Mexico from December 2007 to April 2008. 12 out of the 19 captured sharks were males, one was an adult female, three were juvenile males, and three juvenile females. Four heavy metals (Hg, Pb, Cd, and Cr) and one metaloid (As) were analyzed in shark livers using an atomic absorption spectrophotometry with flame and hydride generator. Our results showed that the maximum concentrations found were: Hg = 0.69 mg/kg, Cd = 0.43 mg/kg, As = 27.37 mg/kg, Cr = 0.70 mg/kg. The minimum concentrations found were: As = 14.91 mg/kg, Cr = 0.35 mg/kg. The Pb could not be determined because the samples did not have the spectrophotometer minimum detectable amount (0.1 mg/kg). None of the 19 samples analyzed showed above the permissible limits established by Mexican and American laws. There was a correlation between shark size and Cr and As concentration (Pearson test). The concentration of Cr and As was observed to be higher in bigger animals. There was not a significant difference in heavy metals concentration between juveniles and adults; however, there was a difference between males and females. A higher Cr concentration was found in females when compared to males. None of the samples exceed the maximum limit established by the laws of Mexico and the United States of America. Much longer studies are needed with C. limbatus and other species caught in the region, in order to determine the degree of contaminants exposure in aquatic ecosystems

Structural and Transition Temperature of HgPbxBa2Ca2Cu3O8+δ Superconductor

International Nuclear Information System (INIS)

Hermiz, G.Y.; Abbass, M.M.

2005-01-01

Solid state reaction technique (SSR) was used to prepare high-T c phase in HgPb x Ba 2 Ca 2 Cu 3 O 8+δ superconductors. The effect of additional Pb to HgBa 2 Ca 2 Cu 3 O 8+δ was investigated. It has been found that the maximum transition temperature T c =133K is at x=0.1.X-ray diffraction showed a tetragonal structure with an average value of e=15.816 A . The average value of the valence of copper (v) is equal to 2.025. There is an increasing of density with the enhancement of the concentration of Pb 2

Phase diagrams of high-order critical phenomene and high-temperature equilibria in the H2O-HgI2-PbI2 system

International Nuclear Information System (INIS)

Valyashko, V.M.; Urusova, M.A.

1996-01-01

The paper studies the principal schemes of complete state diagram of volatile component-two non-volatile components three-component system with tricritical point and sequence of phase transformations at variation of temperature, pressure and composition of mixture. H 2 O-HgI 2 -PbI 2 system, solid phase dissolving process, stratification of solutions and critical phenomena under 200-400 deg C are studied experimentally. General nature of the system phase diagram and parameters of three-phase equilibrium critical point (tricritical point), that is, gas-liquid 1 -liquid 2 are determined. 17 refs., 8 figs., 3 tabs

A High Sensitivity Micro Format Chemiluminescence Enzyme Inhibition Assay for Determination of Hg(II

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Kanchanmala Deshpande

2010-06-01

Full Text Available A highly sensitive and specific enzyme inhibition assay based on alcohol oxidase (AlOx and horseradish peroxidase (HRP for determination of mercury Hg(II in water samples has been presented. This article describes the optimization and miniaturization of an enzymatic assay using a chemiluminescence reaction. The analytical performance and detection limit for determination of Hg(II was optimized in 96 well plates and further extended to 384 well plates with a 10-fold reduction in assay volume. Inhibition of the enzyme activity by dissolved Hg(II was found to be linear in the range 5–500 pg.mL−1 with 3% CVin inter-batch assay. Due to miniaturization of assay in 384 well plates, Hg(II was measurable as low as 1 pg.mL−1 within15 min. About 10-fold more specificity of the developed assay for Hg(II analysis was confirmed by challenging with interfering divalent metal ions such as cadmium Cd(II and lead Pb(II. Using the proposed assay we could successfully demonstrate that in a composite mixture of Hg(II, Cd(II and Pb(II, inhibition by each metal ion is significantly enhanced in the presence of the others. Applicability of the proposed assay for the determination of the Hg(II in spiked drinking and sea water resulted in recoveries ranging from 100–110.52%.

Effects of PbO-B2O3 Glass Doping on the Sintering Temperature and Piezoelectric Properties of 0.35Pb (Ni1/3Nb2/3)O3-0.65Pb(Zr0.41Ti0.59)O3 Ceramics

Science.gov (United States)

Yi, Jinqiao; Shen, Meng; Liu, Sisi; Jiang, Shenglin

2015-12-01

0.35Pb(Ni1/3Nb2/3)O3-0.65Pb(Zr0.41Ti0.59)O3 (PNN-PZT) ceramics doped with 0.5PbO-0.5B2O3 glass have been synthesized by the conventional solid-state sintering technique. The effects of 0.5PbO-0.5B2O3 glass on the sintering temperature and piezoelectric properties of PNN-PZT ceramics were studied. The results indicated that the sintering temperature of PNN-PZT was significantly reduced due to the incorporation of 0.5PbO-0.5B2O3 glass dopant. When the content of 0.5PbO-0.5B2O3 glass was 0.5 wt.%, the sintering temperature of PNN-PZT was observed to reduce from above 1200°C to 920°C while the samples maintained high density (7.91 g/cm3), excellent piezoelectric constant ( d 33 = 479 pC/N), large electromechanical coupling coefficient ( K p = 0.55), and relatively low electromechanical quality factor ( Q m = 79). Moreover, large dielectric constant ( ɛ 33 T / ɛ 0 = 2904) and low dielectric loss (tan δ = 0.0166) were obtained in this work.

Comparative toxicity of heavy metal ions for some microorganisms. [Rhodotorula; Hansenula anormala; T. utilis; Serratia; Azotobacter; Pseudomonas; Escherichia coli; yeasts

Energy Technology Data Exchange (ETDEWEB)

Avakyan, Z A

1967-01-01

Polarographic study of Pb/sup 2 +/, Cd/sup 2 +/, Co/sup 2 +/, and Ni/sup 2 +/ concentration in different media has shown that at pH 6.0, Pb/sup 2 +/ is always precipitated by phosphates and cannot be determined polarographically. Cd, Co and Ni content is somewhat lower than that found in water solutions. The effect of Ag, Hg, Co, Ni, Pb, and Cd ions on the growth of 3 strains of Rhodotorula, Hansenula anomala and T. utilis, 6 strains of Serratia, 6 strains of Azotobacter, 12 strains of Pseudomonas and 2 strains of E. coli was studied. According to their toxicity for the microoganisms tested, heavy metals should be arranged in the following order: Ag>Hg>Cogreater than or equal toNi>Cd. Yeasts are the least sensitive to the action of heavy metals, cf. come serratia, Pseudomonas, Azotobacter and E. coli.

KANDUNGAN Pb, Cd, Hg DALAM AIR MINUM DARI DEPOT AIR MINUM ISI ULANG DI JAKARTA, TANGERANG, DAN BEKASI

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Athena Athena

2012-11-01

Full Text Available A study on chemical quality of drinking water from reffil depots was done in Jakarta, Tangerang, and Bekasi in 2003 to determine the contents of heavy metals such as lead (Pb, cadmium, (Cd, and Mercury (Hg. A total of 38 refill depots was selected as samples. Data were collected by water sampling collection and water analysis, and interview with operators and association personal using questionairs. Water samples were analyzed using Atomic Absorption Spectrophotometer (AAS to examine the contents of their heavy metals based on raw water and drinking water standards. The results showed that the treatment processed were filtration and disinfection. However, the contents of heavy metals in the two types of water samples still complied with the standards stated in Health Ministerial Decree no 906 in the year 2002.   Keywords: heavy metals, drinking water, drinking water refill depots

Interactions of Hg(ii) with oligonucleotides having thymine-thymine mispairs. Optimization of an impedimetric Hg(ii) sensor.

Science.gov (United States)

Kamal, Ajar; She, Zhe; Sharma, Renu; Kraatz, Heinz-Bernhard

2017-05-21

The present work describes the effect of the number of thymine-thymine mispairs in single strand DNA probes on Hg(ii) interactions and further to develop a highly sensitive DNA based impedimetric sensor for Hg(ii) detection. To achieve this goal, the influence of the number of T-T mispairs on the signal response prompted by DNA-Hg(ii) binding interactions was examined on three designed DNA probes: 5'-OH-(CH 2 ) 6 -S-S-(CH 2 ) 6 -AGTCCACACGTTCCTTACGC-3', 5'-OH-(CH 2 ) 6 -S-S-(CH 2 ) 6 -AGTCCACATTTTCCTTTTGC-3', 5'-OH-(CH 2 ) 6 -S-S-(CH 2 ) 6 -AGTCCATTTTTTCCTTTTTT-3' having 2T-T, 4T-T and 6T-T mispairs with identical length, respectively. This study revealed that the number of T-T mispairs plays a critical role in maximizing the signal intensity of DNA-Hg(ii) binding interactions. Based on these results, DNA comprising maximum number of T-T mispairs was further utilized for construction of the Hg(ii) sensor, which exhibited a linear correlation between the change in charge transfer resistance (ΔR CT ) and the concentration of Hg(ii) over the range of 1.0 × 10 -5 M to 1.0 × 10 -10 M with a lower detection limit of 3.2 × 10 -11 M. The selectivity was tested against 12 different metal ions including Hg(ii). The ΔR CT response from Hg(ii) is 3 times higher than the nearest competitor Pb(ii) and approximately 10 times than other ions. The potential application of such a robust and label-free DNA sensor was demonstrated by analyzing environmental samples collected from Lake Ontario.

Spatial distribution and metal contamination in the coastal sediments of Al-Khafji area, Arabian Gulf, Saudi Arabia.

Science.gov (United States)

Alharbi, Talal; Alfaifi, Hussain; Almadani, Sattam A; El-Sorogy, Abdelbaset

2017-11-13

To document the spatial distribution and metal contamination in the coastal sediments of the Al-Khafji area in the northern part of the Saudi Arabian Gulf, 27 samples were collected for Al, V, Cr, Mn, Cu, Zn, Cd, Pb, Hg, Sr, As, Fe, Co, and Ni analysis using inductively coupled plasma-mass spectrometer (ICP-MS). The results revealed the following descending order of the metal concentrations: Sr > Fe > Al > As > Mn > Ni > V > Zn > Cr > Cu > Pb > Co > Hg > Cd. Average levels of enrichment factor of Sr, As, Hg, Cd, Ni, V, Cu, Co, and Pb were higher than 2 (218.10, 128.50, 80.94, 41.50, 12.31, 5.66, 2.95, 2.90, and 2.85, respectively) and that means the anthropogenic sources of these metals, while Al, Zn, Cr and Mn have enrichment factor less than 2, which implies natural sources. Average values of Sr, Hg, Cd, Cr, Ni, and As in the coastal sediments of Al-Khafji area were mostly higher than the values recorded from the background shale and earth crust and from those results along coasts of the Caspian Sea and the Mediterranean Sea. The highest levels of Cu in the northern part of the studied coastline might be due to Al-Khafji desalination plant, while levels of Al, Ni, Cr, Fe, Mn, Pb, and Zn in the central part may be a result of landfilling and industrial sewage. The highest levels of As, Cd, Co, Cu, Hg, and V in the southern part seem to be due to oil pollutants from Khafji Joint Operations (KJO). The higher values of Sr in the studied sediments in general and particularly in locality 7 could relate to the hypersalinity and aragonitic composition of the scleractinian corals abundant in that area.

Study of elastic pion scattering from 9Be, 28Si, 58Ni, and 208Pb at 162 MeV

International Nuclear Information System (INIS)

Devereux, M.J.

1979-05-01

Elastic pion scattering from 9 Be, 28 Si, 58 Ni, and 208 Pb at 162 MeV is analyzed and compared with an optical model theory which incorporates a pion--nucleon range. Excellent fits to the data are obtained in all but one case. The fitted values of the pion--nucleon range, as well as other fitted values are listed. 108 references

Assessment Of Heavy Metal Contamination Of Water Sources From Enyigba Pb-Zn District South Eastern Nigeria

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Nnabo Paulinus N

2015-08-01

Full Text Available Abstract A total of thirty 30 water samples were collected from the Enyigba PbZn mining district to assess the contamination of the water sources as a result of mining of lead and zinc minerals in the area. This comprises of 12 samples of surface water 14 from mine ponds and 4 from underground borehole water. The samples were acidified to stabilize the metals for periods more than four days without the use of refrigeration. The acidified water samples were analysed by a commercial laboratory at Projects Development Institute PRODA Enugu using Atomic Absorption Spectroscopy AAS. The elements determined by this method are lead Pb zinc Zn copper Cu arsenic As cadmium Cd nickel Ni manganese Mn and cobalt Co. The result and analysis of contamination factor showed that in surface water Cd had the highest concentration followed by As and Pb while Ni had the lowest. In mine ponds Cd also had the highest concentration and followed by Pb and As and Ni the lowest. In borehole water Cd has the highest concentration followed by Pb and As while Ni had the lowest concentration. Compared to WHO permissible limits the contamination of the heavy metals in all water sources are in order CdAsPbNiZnCu. In surface water the order is CdAsPbNiZnCu in mine ponds it is CdPbAsNiZnCu and in borehole water the order is CdAsPbZnNiCu. The calculated contamination factors show very high contamination status for Cd Pb and As. These levels of contamination and values indicate that under the prevailing conditions and environmental regulations in Nigeria the mining district would face major and hazardous discharges of these metals to the water sources.

Heavy metals contents in agricultural topsoils in the Ebro basin (Spain). Application of the multivariate geoestatistical methods to study spatial variations

International Nuclear Information System (INIS)

Rodriguez Martin, Jose Antonio; Arias, Manuel Lopez; Grau Corbi, Jose Manuel

2006-01-01

In this work the content of seven heavy metals (Cd, Cr, Cu, Hg, Ni, Pb and Zn) and other parameters (the pH, organic matter, carbonates and granulometric fraction) in agricultural topsoil in the Ebro basin are quantified, based on 624 samples collected according to an 8 by 8 km square mesh. The average concentrations (mg/kg) obtained were: Cd 0.415 ± 0.163, Cr 20.27 ± 13.21, Cu 17.33 ± 14.97, Ni 20.50 ± 22.71, Pb 17.54 ± 10.41, Zn 17.53 ± 24.19 and Hg 35.6 ± 42.05 μg/kg. The concentration levels are relatively low in areas of high pH and low organic matter content concentration. The results of factor analysis group Cd, Cu, Hg, Pb and Zn in F1 and Cr y Ni in F2. The spatial heavy metals component maps based on geostatistical analysis, show definite association of these factors with the soil parent material. The local anomalies (found in Cu, Zn and Pb) are attributed to anthropogenic influence. - Geostatistical analyses showed definite association of metals with soil parent materials

Synthesis and magnetic properties of multilayer Ni/Cu and NiFe/Cu ...

Indian Academy of Sciences (India)

The diameter of wires can be easily varied by pore size of alumina, ranging ... saturated HgCl2 solution to remove the remaining Al, and then dipped in 5 wt% ... for NiFe alloy it is 1.3 V, that is higher than for Ni/Cu nanowires to diminish Cu.

Interaction of Cr (III), Ni (II), Pb (II) with DTPA complexes of essential metal ions

International Nuclear Information System (INIS)

Gulzar, S.; Zahida; Maqsood, T.; Naqvi, R.R.

2002-01-01

With the increase of anthropogenic activities in the environment, heavy metal toxicity (Chromium, Nickel and Lead) is more common now. DTPA (diethylene triamine pentaacetic acid) a polyamino carboxylic acid is widely used to form hydrophilic and stable complexes with most of the metal ions. In this spectrophotometric study, concentration of Cr(III), Ni(II) and Pb(II) (toxic metal ions) exchanged with Fe(III), Zn(II) and Ca(II) from their DTPA complexes were estimated at pH 4,7 and 9. Concentration of added metal was varied from 1-4 times to that of complexed metal. (author)

Pb3O4 type antimony oxides MSb2O4 (M = Co, Ni) as anode for Li-ion batteries

International Nuclear Information System (INIS)

Jibin, A.K.; Reddy, M.V.; Subba Rao, G.V.; Varadaraju, U.V.; Chowdari, B.V.R.

2012-01-01

Graphical abstract: Isostructural Pb 3 O 4 type MSb 2 O 4 (M = Co, Ni) compounds were investigated as possible anodes for lithium ion batteries. The reversible capacity is due to electrochemically active Sb and the transition metal and Li 2 O form an inactive matrix which buffers volume variations associated with alloying-de-alloying of antimony. Highlights: ► Isostructural MSb 2 O 4 (M = Co, Ni) were studied as anode for LIBs for first time. ► Li/MSb 2 O 4 (M = Co, Ni) cells displayed reversibility due to electrochemically active Sb. ► CoSb 2 O 4 showed good reversibility compared to NiSb 2 O 4 . - Abstract: Polycrystalline samples of isostructural MSb 2 O 4 (M = Co, Ni) have been prepared by solid state synthesis and lithium-storage is investigated as possible anode materials for lithium-ion batteries. The reaction mechanism of lithium with MSb 2 O 4 (M = Co, Ni) is explored by galvanostatic cycling, cyclic voltammogram and ex situ studies. Both CoSb 2 O 4 and NiSb 2 O 4 exhibit similar electrochemical behavior and show reversible capacity of 490 and 412 mAh g −1 respectively in the first cycle. Reversible alloying de-alloying of Li x Sb takes place in an amorphous matrix of M (Co, Ni) and Li 2 O during electrochemical cycling.

Toxicity of some metals on the fish Therapon Jarbua (Forsskal, 1775)

Digital Repository Service at National Institute of Oceanography (India)

Krishnakumari, L.; Varshney, P.K.; Gajbhiye, S.N.; Govindan, K.; Nair, V.R.

Hg, V and Pb were more toxic to Therapon jarbua than the other metals studied. Recorded 86 h LC sub(50) for Hg, V, Pb, As, Cu, Zn, Ni and Co was respectively at 0.06, 0.62, 1.23, 3.38, 4.5, 11.0, 19.4 and 52.5 mg.l/1. The 90% survival for 96 h...

Accumulation of elements by edible mushroom species: part I. Problem of trace element toxicity in mushrooms.

Science.gov (United States)

Mleczek, Mirosław; Siwulski, Marek; Stuper-Szablewska, Kinga; Rissmann, Iwona; Sobieralski, Krzysztof; Goliński, Piotr

2013-01-01

The aim of this study was to evaluate Cd, Co, Cu, Hg, Ni, Pb, Sr and Zn accumulation in six edible mushroom species and to assess their risk and benefits to human consumers. Mushrooms (Leccinium aurantiacum, Xerocomus badius, Lactarius deliciosus, Boletus edulis, Cantharellus cibarius and Suillus luteus) were collected from selected regions of Poland during 1990-2010. The highest diversity between studied mushroom species was observed in terms of Cu and Zn accumulation. Significant differences in the accumulation efficiency were found among the six mushroom species examined. The most efficient were Boletus edulis (Cd and Hg), Suillus luteus (Cu and Sr), and Lactarius deliciosus (Pb and Zn). In the case of Co and Ni, the most effective were Xerocomus badius and Leccinium aurantiacum, respectively. The calculated bioconcentration factor (BCF) values of Cd, Cu, Hg, Sr and Zn were > 1 for all species in this study while Co, Ni and Pb usually were bioexcluded (BCF luteus collected in Poland is safe and this finding largely agrees with results from recent studies by other authors.

E2 and M1 Transition Probabilities in Odd Mass Hg Nuclei

Energy Technology Data Exchange (ETDEWEB)

Berg, V; Baecklin, A; Fogelberg, B; Malmskog, S G

1969-10-15

L- and M-subshell ratios have been measured for the 39.5 keV transition in {sup 193}Hg and the 37.1 and 16.2 keV transitions in {sup 195}Hg yielding 0.38 {+-} 0.12 , <0.02 and 0.08 {+-} 0.03 per cent E2, respectively. The half-lives of the 39.5 keV level in {sup 193}Hg and the 53.3 and 37.1 keV levels in {sup 195}Hg have been measured by the delayed coincidence method, yielding values of 0.63 {+-} 0.03, 0.72 {+-} 0.03 and <0.05 nsec respectively. A systematic compilation of reduced E2 and M1 transition probabilities in odd mass Pt, Hg and Pb nuclei is given and compared to theoretical predictions.

Subcellular partitioning of non-essential trace metals (Ag, As, Cd, Ni, Pb, and Tl) in livers of American (Anguilla rostrata) and European (Anguilla anguilla) yellow eels

Energy Technology Data Exchange (ETDEWEB)

Rosabal, Maikel [Institut national de la recherche scientifique, Centre Eau Terre et Environnement (INRS–ETE), 490 de la Couronne, Québec (Québec) G1K 9A9 (Canada); Pierron, Fabien [Université de Bordeaux, UMR EPOC CNRS 5805, F-33400 Talence (France); CNRS, EPOC, UMR 5805, F-33400 Talence (France); Couture, Patrice [Institut national de la recherche scientifique, Centre Eau Terre et Environnement (INRS–ETE), 490 de la Couronne, Québec (Québec) G1K 9A9 (Canada); Baudrimont, Magalie [Université de Bordeaux, UMR EPOC CNRS 5805, F-33400 Talence (France); CNRS, EPOC, UMR 5805, F-33400 Talence (France); Hare, Landis [Institut national de la recherche scientifique, Centre Eau Terre et Environnement (INRS–ETE), 490 de la Couronne, Québec (Québec) G1K 9A9 (Canada); Campbell, Peter G.C., E-mail: peter.campbell@ete.inrs.ca [Institut national de la recherche scientifique, Centre Eau Terre et Environnement (INRS–ETE), 490 de la Couronne, Québec (Québec) G1K 9A9 (Canada)

2015-03-15

Highlights: • Handling of hepatic metals consistently involved cytosolic, thermostable ligands. • Granule-like fractions are also involved in the detoxification of Ni, Pb, and Tl. • Despite these sequestration mechanisms, metal detoxification is incomplete. • Along the metal gradient, concentrations increase in metal-sensitive fractions. • This increase could represent a toxicological risk for the yellow eels. - Abstract: We determined the intracellular compartmentalization of the trace metals Ag, As, Cd, Ni, Pb, and Tl in the livers of yellow eels collected from the Saint Lawrence River system in Canada (Anguilla rostrata) and in the area of the Gironde estuary in France (Anguilla anguilla). Differential centrifugation, NaOH digestion and thermal shock were used to separate eel livers into putative “sensitive” fractions (heat-denatured proteins, mitochondria and microsomes + lysosomes) and detoxified metal fractions (heat-stable peptides/proteins and granules). The cytosolic heat-stable fraction (HSP) was consistently involved in the detoxification of all trace metals. In addition, granule-like structures played a complementary role in the detoxification of Ni, Pb, and Tl in both eel species. However, these detoxification mechanisms were not completely effective because increasing trace metal concentrations in whole livers were accompanied by significant increases in the concentrations of most trace metals in “sensitive” subcellular fractions, that is, mitochondria, heat-denatured cytosolic proteins and microsomes + lysosomes. Among these “sensitive” fractions, mitochondria were the major binding sites for As, Cd, Pb, and Tl. This accumulation of non-essential metals in “sensitive” fractions likely represents a health risk for eels inhabiting the Saint Lawrence and Gironde environments.

Structural characterization of PbTi03, Sm0.6Nd0.4NiO3 and NdMnO3 multifunctional Perovskite thin films

Directory of Open Access Journals (Sweden)

Rapenne L.

2012-06-01

Full Text Available Different multifunctional (PbTiO3, Sm0.6Nd0.4NiO3, NdMnO3 thin films were grown by metalorganic chemical vapor deposition (MOCVD technique on SrTiO3 and LaAlO3 substrates. TEM and X-ray diffraction measurements reveal that almost single crystalline thin films can be epitaxially grown on the top of substrates. The relationship between the crystallographic orientation of the films and those of the substrates were determined by reciprocal space mapping and TEM analyses. PbTi03 thin films appear to be under tensile or compressive strain according to the different mismatch of their cell parameter with those of the substrate. Relaxation mechanism as a function of the film thickness arises from coexistence of different type of domains and size and strain effect are analyzed. SmNiO3 thin films present diffuse scattering strikes and are less well organized when compared to PbTi03 thin films. Different domains are observed as well as an additional parasitic phase close to NiO. Its regular distribution can be associated to reduced transport properties. Preliminary observations on NdMnO3 thin films show that an amorphous phase is obtained during MOCVD that can be transformed in a single crystalline film by annealing. The films are under tensile or compressive strain according to the different mismatch of their cell parameter with those of the substrate. Magnetic properties are investigated.

Transformation of technogenic compounds of Ni, Cu, Zn and Pb in different soil types in model experiment

International Nuclear Information System (INIS)

Ladonin, D.V.; Smirnova, M.S.; Karpukhin, M.M.; Plyaskina, O.V.

2008-01-01

In model experiment fractional distribution of Ni, Cu, Zn and Pb in soils artificially polluted with readily and sparingly soluble compounds (nitrates and oxides respectively) of these heavy metals was investigated. It is shown that heavy metals fractional distribution may strongly vary depending on the form in which the metal deposits in the soil. Transformation of heavy metals oxides is controlled by two main factors: solubility of an oxide and characteristics of reactions between dissolution products and the soil components

Removal of Ni(II), Zn(II) and Pb(II) ions from single metal aqueous solution using rice husk-based activated carbon

Energy Technology Data Exchange (ETDEWEB)

Taha, Mohd F., E-mail: faisalt@petronas.com.my; Shaharun, Maizatul S. [Fundamental and Applied Sciences Department, Universiti Teknologi PETRONAS, Bandar Seri Iskandar, 31750, Perak Darul Ridzuan (Malaysia); Shuib, Anis Suhaila, E-mail: anisuha@petronas.com.my; Borhan, Azry [Chemical Engineering Department, Universiti Teknologi PETRONAS, Bandar Seri Iskandar, 31750, Perak Darul Ridzuan (Malaysia)

2014-10-24

An attempt was made to investigate the potential of rice husk-based activated carbon as an alternative low-cost adsorbent for the removal of Ni(II), Zn(II) and Pb(II) ions from single aqueous solution. Rice husk-based activated carbon was prepared via treatment of rice husk with NaOH followed by the carbonization process at 400°C for 2 hours. Three samples, i.e. raw rice husk, rice husk treated with NaOH and rice husk-based activated carbon, were analyzed for their morphological characteristics using field-emission scanning electron microscope/energy dispersive X-ray (FESEM/EDX). These samples were also analyzed for their carbon, hydrogen, nitrogen, oxygen and silica contents using CHN elemental analyzer and FESEM/EDX. The porous properties of rice husk-based activated carbon were determined by Brunauer-Emmett-Teller (BET) surface area analyzer, and its surface area and pore volume were 255 m{sup 2}/g and 0.17 cm{sup 2}/g, respectively. The adsorption studies for the removal of Ni(II), Zn(II) and Pb(II) ions from single metal aqueous solution were carried out at a fixed initial concentration of metal ion (150 ppm) with variation amount of adsorbent (rice husk-based activated carbon) as a function of varied contact time at room temperature. The concentration of each metal ion was analyzed using atomic absorption spectrophotometer (AAS). The results obtained from adsorption studies indicate the potential of rice husk as an economically promising precursor for the preparation of activated carbon for removal of Ni(II), Zn(II) and Pb(II) ions from single aqueous solution. Isotherm and kinetic model analyses suggested that the experimental data of adsorption studies fitted well with Langmuir, Freundlich and second-order kinetic models.

[Determination of total mass and morphology analysis of heavy metal in soil with potassium biphthalate-sodium hydroxide by ICP-AES].

Science.gov (United States)

Qu, Jiao; Yuan, Xing; Cong, Qiao; Wang, Shuang

2008-11-01

Blank soil was used as quality controlling samples, soil sample dealt by potassium biphthalate-sodium hydroxide buffer solution was used as check sample, mixed acid HNO3-HF-HClO4 was chosen to nitrify soil samples, and plasma emission spectrometer (ICP-AES) was used as detecting method. The authors determined the total metal mass of Mo, Pb, As, Hg, Cr, Cd, Zn, Cu and Ni in the extracted and dealt soil samples, and determined the mass of Mo, Pb, As, Hg, Cr, Cd, Zn, Cu and Ni in the three chemical morphologies, including acid extractable morphology, oxide associated morphology, and organics associated modality. The experimental results indicated that the different pH of potassium biphthalate-sodium hydroxide buffer solution had obvious influence on the total mass of heavy metal and morphology transformation. Except for metal element Pb and Zn, the addition of different pH potassium dihydrogen phosphate-sodium hydroxide buffer solution could accelerate the soil samples nitrification and the total mass determination of heavy metal in the soil samples. The potassium biphthalate-sodium hydroxide buffer solution could facilitate the acid extractable morphology of Cr, Cu, Hg and Pb, oxidation associated morphology of As, Hg, Pb and Zn and the organic associated morphology transforming of As and Hg. At pH 5.8, the maximum acid extractable morphology contents of Cu and Hg were 2.180 and 0.632 mg x kg(-1), respectively; at pH 6.2, the maximal oxidation associated morphology content of Pb could achieve 27.792 mg x kg(-1); at pH 6.0, the maximum organic associated morphology content of heavy metal Hg was 4.715 mg x kg(-1).

Experiments on multi-nucleon transfer reactions with the systems {sup 58,64}Ni+{sup 207}Pb at SHIP

Energy Technology Data Exchange (ETDEWEB)

Fernandovich Comas Lijachev, Victor

2012-07-01

This work presents experimental results on multi-nucleon transfer reactions in the collision systems {sup 58}Ni+{sup 207}Pb and {sup 64}Ni+{sup 207}Pb which were measured at the velocity filter SHIP at GSI. The reactions were performed at beam energies below and up to 10% above the Coulomb barrier. The work was motivated by theoretical predictions to apply multi-nucleon transfer reactions in heavy systems to synthesize new neutron-rich isotopes in the region of superheavy nuclei with Z>100 and in the region of the closed neutron shell N=126. The expected cross-sections for the production of these nuclei in transfer reactions are small and reach typically nanobarn and below. Therefore, efficient separation techniques have to be applied and the detection system must allow for the identification of single nuclei. A dedicated experimental setup to study such rare transfer products does not exist presently. But already existing facilities which are used for the synthesis of superheavy fusion products meet the requirements for the detection of rare reaction products. In this context, the velocity filter SHIP offers the possibility to separate heavy target-like transfer products from projectiles and projectile-like reaction products before they reach the detection system where the particles are identified by their alpha-decay properties. At SHIP, a cross-section limit of 10 pb can be reached at usual beam intensities. In the present work on collisions of {sup 58,64}Ni+{sup 207}Pb the influence of the projectile neutron number on the cross-sections, isotopic distributions and excitation energies of the transfer products was studied. Especially with the more neutron-rich {sup 64}Ni projectiles a transfer of up to seven protons and eight neutrons to the target nucleus was observed. The largest cross-sections for the most neutron-rich isotopes were reached at the beam energies around the Coulomb barrier. The transfer was accompanied by the full dissipation of the available

The structural, electronic, magnetic, and mechanical properties of perovskite oxides PbM1/2Nb1/2O3 (M = Fe, Co and Ni)

Science.gov (United States)

Erkisi, A.; Surucu, G.; Deligoz, E.

2018-03-01

In this study, the structural, electronic, magnetic, and mechanical properties of perovskite oxides PbM1/2Nb1/2O3 (M = Fe, Co and Ni) are investigated. The systems are treated in ferromagnetic order. The calculations are carried out in the framework of density functional theory (DFT) within the plane-wave pseudopotential method. The exchange-correlation potential is approximated by generalized-gradient spin approach (GGA). The intra-atomic Coulomb repulsion is also taken into account in calculations (GGA + U). We have considered two generalized-gradient spin approximation functionals, which are Perdew-Burke-Ernzerhof (PBE) and PBE for solids (PBEsol) for structural parameter calculations when it included Hubbard potential. Although the spin-polarized electronic band structures of PbCo1/2Nb1/2O3 and PbNi1/2Nb1/2O3 systems exhibit metallic property in ferromagnetic phase, a bandgap is observed in spin-down states of PbFe1/2Nb1/2O3 resulting in half-metallic behavior. The main reason for this behavior is attributed to the hybridization between d-states of transition metal atoms and p-states of oxygen atoms. The stability mechanically and the calculated mechanical properties by using elastic constants show that these compounds are mechanically stable in tetragonal phase and have anisotropic character mechanically.

CORRELATION OF THE PARTITIONING OF DISSOLVED ORGANIC MATTER FRACTIONS WITH THE DESORPTION OF CD, CU, NI, PB AND ZN FROM 18 DUTCH SOILS

Science.gov (United States)

Eighteen Dutch soils were extracted in aqueous solutions at varying pH. Extracts were analyzed for Cd, Cu, Ni, Pb and Zn by ICP-AES. Extract dissolved organic carbon (DOC) was also concentrated onto a macroreticular resin and fractionation into three operationally defined fract...

Cr, Cu, Hg and Ni release from incineration bottom ash during utilization in land reclamation - based on lab-scale batch and column leaching experiments and a modeling study.

Science.gov (United States)

Yin, Ke; Chan, Wei Ping; Dou, Xiaomin; Ren, Fei; Wei-Chung Chang, Victor

2018-04-01

Incineration bottom ash (IBA) as potential material for land reclamation was investigated, based on leaching tests, sorption studies and simulation models. Based on batch and column leaching tests, Cr, Cu, Hg and Ni in the IBA leachates were measured as high as 510 μg/L, 20330 μg/L, 5.1 μg/L and 627 μg/L, respectively, presenting potential environmental risks. Sorption study was then performed with various concentrations of IBA leachates on sands and excavated materials. Partitioning coefficients of targeting metals were determined to be 6.5 (Cr), 18.4 (Cu), 16.6 (Hg), and 1.8 (Ni) for sands, while 17.4 (Cr), 13.6 (Cu), 67.1 (Hg), and 0.9 (Ni) for excavated materials, much lower than literature in favor of their transportation. Deterministic and Monte Carlo simulation was further performed under designated boundaries, combined with measured geotechnical parameters: density, porosity, permeability, partitioning coefficient, observed diffusivity, hydraulic gradient, etc., to quantitatively predict metals' fate during IBA land reclamation. Environmental risks were quantitatively unveiled in terms of predicted time of breakthrough for the targeting metals (comparing to US EPA criterion for maximum or continuous concentration). Sands were of little effects for all metals' breakthrough (1 month or less) under advection, while excavated materials sufficiently retained metals from thousands up to millions of years, under diffusion or advection. Permeability next to the IBA layer as the major risk-limiting factor, dominated transport of IBA leachates into the field. The current study provides discrimination of environmental risks associated with metals and a quantitative guidance of project design for IBA utilization in land reclamation. Copyright © 2018 Elsevier Ltd. All rights reserved.

Preparation, characterization and evaluation of water-soluble L-cysteine-capped-CdS nanoparticles as fluorescence probe for detection of Hg(II) in aqueous solution

International Nuclear Information System (INIS)

Cai Zhaoxia; Yang Hong; Zhang Yi; Yan Xiuping

2006-01-01

Water-soluble L-cysteine-capped-CdS nanoparticles were prepared in aqueous solution at room temperature through a straightforward one-pot process by using safe and low-cost inorganic salts as precursors, and characterized by transmission electron microscopy, X-ray diffraction spectrometry, Fourier transform infrared spectrometry, spectrofluorometry and ultraviolet-visible spectrometry. The prepared L-cysteine-capped-CdS nanoparticles were evaluated as fluorescence probe for Hg(II) detection. The fluorescence quenching of the L-cysteine-capped-CdS nanoparticles depended on the concentration and pH of Hg(II) solution. Maximum fluorescence quenching was observed at pH 7.4 with the excitation and emission wavelengths of 360 nm and 495 nm, respectively. Quenching of its fluorescence due to Hg(II) at the 20 nmol l -1 level was unaffected by the presence of 5 x 10 6 -fold excesses of Na(I) and K(I), 5 x 10 5 -fold excesses of Mg(II), 5 x 10 4 -fold excesses of Ca(II), 500-fold excesses of Al(III), 91-fold excesses of Mn(II), 23.5-fold excesses of Pb(II), 25-fold excesses of Fe(III), 25-fold excesses of Ag(I), 8.5-fold excesses of Ni(II) and 5-fold excesses of Cu(II). Under optimal conditions, the quenched fluorescence intensity increased linearly with the concentration of Hg(II) ranging from 16 nmol l -1 to 112 nmol l -1 . The limit of detection for Hg(II) was 2.4 nmol l -1 . The developed method was applied to the detection of trace Hg(II) in aqueous solutions

Use of Aloe vera shell ash supported Ni0.5Zn0.5Fe2O4 magnetic nanoparticles for removal of Pb (II from aqueous solutions

Directory of Open Access Journals (Sweden)

Samira Namavari

2016-03-01

Full Text Available Background: Lead (Pb is a heavy metal that is widely utilized in industries. It contaminates soil and groundwater. Its non-biodegradability, severe toxicity, carcinogenicity, ability to accumulate in nature and contaminate groundwater and surface water make this toxic heavy metal extremely dangerous to living beings and the environment. Therefore, technical and economic methods of removing Pb are of great importance. This study evaluated the efficiency of Ni0.5Zn0.5Fe2O4 magnetic nanoparticles supported by Aloe vera shell ash in removing Pb from aqueous environments. Methods: The adsorbent was characterized by several methods, including x-ray diffraction (XRD, scanning electron microscopy (SEM, and Fourier transform infrared spectroscopy (FT-IR. Then, the potential of Aloe vera shell ash-supported Ni0.5Zn0.5Fe2O4 magnetic nanoparticles to adsorb Pb (II was investigated. To determine the amount of lead absorbed by this adsorbent, different pHs (2, 4, 5, and 6, adsorbent doses (0.01-0.40 g, Pb concentrations (5, 10, 20, 30, 40, 50, 60, 80, 100, 200, 300, and 600 mg/L, and exposure times (0, 5, 10, 15, 20, 30, 40, 50, and 60 minutes until reaching equilibrium were tested using an atomic absorption spectrometer (Varian-AA240FS. Residual concentrations of Pb were read. Results: The results show that a time of 15 minutes, pH value of 9, and adsorbent dose of 0.2 g are the optimum conditions for Pb (II removal by this adsorption process. Increasing the initial concentration of Pb (II from 5 to 600 mg/L decreased removal efficiency from 98.8% to 73%. The experimental data fit well into the Freundlich isotherm model (R2 = 0.989. Conclusion: Ni0.5Zn0.5Fe2O4 magnetic nanoparticles supported by Aloe vera shell ash comprise a low-cost, simple, and environmentally benign procedure. The maximum monolayer adsorption capacity based on the Langmuir isotherm (R2 = 0.884 is 47.2 mg g-1. The prepared magnetic adsorbent can be well dispersed in aqueous solutions and

Determination of As, Cd, Hg and Pb in continuous use drugs and excipients by plasma-based techniques in compliance with the United States Pharmacopeia requirements

Science.gov (United States)

da Silva, Caroline Santos; Pinheiro, Fernanda Costa; do Amaral, Clarice Dias Britto; Nóbrega, Joaquim Araújo

2017-12-01

Some inorganic impurities are toxic to human health even when present at low concentrations and therefore must be carefully monitored in products as continuous use drugs. This work aimed the development of a simple microwave-assisted digestion procedure for different types of drugs and excipients and the analytical determination of elemental impurities according to the new regulations of the United States Pharmacopeia (USP) 232 and 233 using inductively coupled plasma optical emission spectrometry (ICP-OES) or inductively coupled plasma mass spectrometry (ICP-MS). Eight drugs samples and two excipients of different brands were microwave-assisted digested with inverse aqua regia. Addition and recovery experiments were performed according to J values, once permissible daily exposure value is specific for each element and estimated according to the maximum daily dose of drug indicated by the label. Samples were spiked with values of 1.5J in order to check accuracies for As, Cd, Hg, and Pb. Recoveries obtained by ICP-OES ranged from 75 to 148% and for ICP-MS ranged from 74 to 120%. The limits of detection for ICP-OES ranged from 0.4 to 17 mg kg- 1 and for ICP-MS from 7.4 to 41.6 μg kg- 1. Both analytical methods were adequate in terms of accuracies and sensitivities. Considering the maximum daily dose, all drugs samples and excipients contained As, Cd, Hg and Pb below the maximum limits stipulated by USP since all of them presented contents below respective limits of detection.

Soldering-induced Cu diffusion and intermetallic compound formation between Ni/Cu under bump metallization and SnPb flip-chip solder bumps

Science.gov (United States)

Huang, Chien-Sheng; Jang, Guh-Yaw; Duh, Jenq-Gong

2004-04-01

Nickel-based under bump metallization (UBM) has been widely used as a diffusion barrier to prevent the rapid reaction between the Cu conductor and Sn-based solders. In this study, joints with and without solder after heat treatments were employed to evaluate the diffusion behavior of Cu in the 63Sn-37Pb/Ni/Cu/Ti/Si3N4/Si multilayer structure. The atomic flux of Cu diffused through Ni was evaluated from the concentration profiles of Cu in solder joints. During reflow, the atomic flux of Cu was on the order of 1015-1016 atoms/cm2s. However, in the assembly without solder, no Cu was detected on the surface of Ni even after ten cycles of reflow. The diffusion behavior of Cu during heat treatments was studied, and the soldering-process-induced Cu diffusion through Ni metallization was characterized. In addition, the effect of Cu content in the solder near the solder/intermetallic compound (IMC) interface on interfacial reactions between the solder and the Ni/Cu UBM was also discussed. It is evident that the (Cu,Ni)6Sn5 IMC might form as the concentration of Cu in the Sn-Cu-Ni alloy exceeds 0.6 wt.%.

Metal transfer to plants grown on a dredged sediment: use of radioactive isotope 203Hg and titanium

International Nuclear Information System (INIS)

Caille, Nathalie; Vauleon, Clotilde; Leyval, Corinne; Morel, Jean-Louis

2005-01-01

Improperly disposed of dredged sediments contaminated with metals may induce long-term leaching and an increase of metal concentrations in ground waters and vegetal cover plants. The objective of the study was to quantify the sediment-to-plant transfer of Cu, Pb, Hg and Zn with a particular focus on the pathway of Hg and to determine whether the establishment of vegetal cover modifies the metal availability. A pot experiment with rape (Brassica napus), cabbage (Brassica oleraccea) and red fescue (Festuca rubra) was set up using a sediment first spiked with the radioisotope 203 Hg. Zinc concentrations (197-543 mg kg -1 DM) in leaves were higher than Cu concentration (197-543 mg kg -1 DM), Pb concentration (2.3-2.6 mg kg -1 DM) and Hg concentration (0.9-1.7 mg kg -1 DM). Leaves-to-sediment ratios decreased as follows: Zn>Cu>Hg>Pb. According to Ti measurements, metal contamination by dry deposition was less than 1%. Mercury concentration in plant leaves was higher than European and French thresholds. Foliar absorption of volatile Hg was a major pathway for Hg contamination with a root absorption of Hg higher in rape than in cabbage and red fescue. Growth of each species increased Cu solubility. Zinc solubility was increased only in the presence of rape. The highest increase of Cu solubility was observed for red fescue whereas this species largely decreased Zn solubility. Dissolved organic carbon (DOC) measurements suggested that Cu solubilisation could result from organic matter or release of natural plant exudates. Dissolved inorganic carbon (DIC) measures suggested that the high Zn solubility in the presence of rape could originate from a generation of acidity in rape rhizosphere and a subsequent dissolution of calcium carbonates. Consequently, emission of volatile Hg from contaminated dredged sediments and also the potential increase of metal solubility by a vegetal cover of grass when used in phytostabilisation must be taken into account by decision makers

Metal transfer to plants grown on a dredged sediment: use of radioactive isotope 203Hg and titanium.

Science.gov (United States)

Caille, Nathalie; Vauleon, Clotilde; Leyval, Corinne; Morel, Jean-Louis

2005-04-01

Improperly disposed of dredged sediments contaminated with metals may induce long-term leaching and an increase of metal concentrations in ground waters and vegetal cover plants. The objective of the study was to quantify the sediment-to-plant transfer of Cu, Pb, Hg and Zn with a particular focus on the pathway of Hg and to determine whether the establishment of vegetal cover modifies the metal availability. A pot experiment with rape (Brassica napus), cabbage (Brassica oleraccea) and red fescue (Festuca rubra) was set up using a sediment first spiked with the radioisotope 203Hg. Zinc concentrations (197-543 mg kg(-1) DM) in leaves were higher than Cu concentration (197-543 mg kg(-1) DM), Pb concentration (2.3-2.6 mg kg(-1) DM) and Hg concentration (0.9-1.7 mg kg(-1) DM). Leaves-to-sediment ratios decreased as follows: Zn > Cu > Hg > Pb. According to Ti measurements, metal contamination by dry deposition was less than 1%. Mercury concentration in plant leaves was higher than European and French thresholds. Foliar absorption of volatile Hg was a major pathway for Hg contamination with a root absorption of Hg higher in rape than in cabbage and red fescue. Growth of each species increased Cu solubility. Zinc solubility was increased only in the presence of rape. The highest increase of Cu solubility was observed for red fescue whereas this species largely decreased Zn solubility. Dissolved organic carbon (DOC) measurements suggested that Cu solubilisation could result from organic matter or release of natural plant exudates. Dissolved inorganic carbon (DIC) measures suggested that the high Zn solubility in the presence of rape could originate from a generation of acidity in rape rhizosphere and a subsequent dissolution of calcium carbonates. Consequently, emission of volatile Hg from contaminated dredged sediments and also the potential increase of metal solubility by a vegetal cover of grass when used in phytostabilisation must be taken into account by decision

Soil-plant abstract of heavy metals in Pb-Zn mining sites from Alcudia Valley (South Spain)

Science.gov (United States)

López-Berdonces, Miguel; Higueras, Pablo; Esbrí, Jose Maria; González-Corrochano, Beatríz; García-Noguero, Eva Mª; Martínez-Coronado, Alba; Fernandez-Calderón, Sergio; García-Noguero, Carolina

2013-04-01

with R²= 95. Total metal contents in soils were analyzed by EDXRF (Energy Dispersion X Ray Fluorescence). We obtained RRL (Regional Reference Level), from La Bienvenida soil samples with values 20 Ni; 53 Cr; 38 Cu; 125 Zn; 128 Pb; 26 As, all in mg kg¯¹. Taking into account the values obtained in S.Quintin Pb 10127; Zn 2861; As 183; Cd 138; Cu 331; Ni 60 and Hg 893 mg kg¯¹, we can say that S.Quintin is a highly contaminated area; Bombita and Romanilla we would consider polluted areas where only Ni, As have values below RRL. We found differences in uptake patterns on the three areas due to heterogeneity in soil parameters and acid drainage, especially in S.Quintín mine where only measured uptake of Sb by plant has a good linear correlation with metal content extract with Ammonium Acetate. Romanilla has more homogeneous soil condition where we found an high soil-plant correlation Ag, As, Cd, Zn using EDTA and Acetate. Bombita has a similar characteristics, with high correlations between plants contents and soil in Cd, Cu, Pb, Zn with EDTA and Acetate. Total contents of heavy metal in a soil is not enough to evaluate the Toxicity Potential, it is necessary to know the bioavailable fraction present in the soil and the extractable fraction which proved to be the decisive factor in the content of heavy metal in plant of studied areas; the correlation in metals content soil-plant is higher in extractable content metals than in total content.

Assessing the natural recovery of a lake contaminated with Hg using estimated recovery rates determined by sediment chronologies

International Nuclear Information System (INIS)

Parsons, Matthew J.; Long, David T.; Yohn, Sharon S.

2010-01-01

Research highlights: → Identifying the cause of Hg contamination via correlations to iron ore production. → Using Hg:Al ratio to show changes in pathway from a point to non-point source. → Overcoming challenges to age determination using event-based dating. → Using sediment cores to estimate recovery rates and identify arrested recovery. - Abstract: Deer Lake is an impoundment located near Ishpeming, Michigan, USA. Iron mining assay laboratories located in Ishpeming disposed of Hg salts to the city sewer whose outfall was located along an inlet to Deer Lake. An effort to remediate the system in the mid 1980s which consisted of drawing down water in the impoundment in order to volatize Hg from the sediments did not result in recovery of the system. Since the mid 1990s, the remediation strategy has been to allow the continual burial of the contaminated sediments, i.e., natural recovery. The goal of this study was to assess the effectiveness of this strategy. This was accomplished by investigating State of the system in terms of its recovery and estimating the time frame for recovery. Sediment cores were collected in 2000 to determine historical trends in accumulation rates and concentrations of Hg and other metals. Sedimentation rates and sediment ages were estimated using 210 Pb. Event-based dating (e.g., peak of 137 Cs in 1963) was used to supplement 210 Pb data due to non-monotonic features in the 210 Pb profile and activities that were not at supported levels at the base of the core. Selected results are that: (1) drawdown significantly influenced sedimentation patterns causing slopes for 210 Pb profiles that reflected the influx of older sediment, (2) periods of Fe production correlate to Hg loading indicating the point source for contamination, a relationship not previously identified, (3) Hg:Al ratios indicate a recent change to a watershed pathway for Hg loading and (4) Hg concentrations had decreased from their peak, remain elevated, and were

Assessing the natural recovery of a lake contaminated with Hg using estimated recovery rates determined by sediment chronologies

Energy Technology Data Exchange (ETDEWEB)

Parsons, Matthew J. [Michigan State University, Department of Geological Sciences, 206 Natural Science, East Lansing, MI 48824 (United States); Long, David T., E-mail: long@msu.edu [Michigan State University, Department of Geological Sciences, 206 Natural Science, East Lansing, MI 48824 (United States); Yohn, Sharon S. [Juniata College, Raystown Field Station, Brumbaugh Academic Center, Huntingdon, PA 16652 (United States)

2010-11-15

Research highlights: {yields} Identifying the cause of Hg contamination via correlations to iron ore production. {yields} Using Hg:Al ratio to show changes in pathway from a point to non-point source. {yields} Overcoming challenges to age determination using event-based dating. {yields} Using sediment cores to estimate recovery rates and identify arrested recovery. - Abstract: Deer Lake is an impoundment located near Ishpeming, Michigan, USA. Iron mining assay laboratories located in Ishpeming disposed of Hg salts to the city sewer whose outfall was located along an inlet to Deer Lake. An effort to remediate the system in the mid 1980s which consisted of drawing down water in the impoundment in order to volatize Hg from the sediments did not result in recovery of the system. Since the mid 1990s, the remediation strategy has been to allow the continual burial of the contaminated sediments, i.e., natural recovery. The goal of this study was to assess the effectiveness of this strategy. This was accomplished by investigating State of the system in terms of its recovery and estimating the time frame for recovery. Sediment cores were collected in 2000 to determine historical trends in accumulation rates and concentrations of Hg and other metals. Sedimentation rates and sediment ages were estimated using {sup 210}Pb. Event-based dating (e.g., peak of {sup 137}Cs in 1963) was used to supplement {sup 210}Pb data due to non-monotonic features in the {sup 210}Pb profile and activities that were not at supported levels at the base of the core. Selected results are that: (1) drawdown significantly influenced sedimentation patterns causing slopes for {sup 210}Pb profiles that reflected the influx of older sediment, (2) periods of Fe production correlate to Hg loading indicating the point source for contamination, a relationship not previously identified, (3) Hg:Al ratios indicate a recent change to a watershed pathway for Hg loading and (4) Hg concentrations had decreased from

Vibrational spectroscopic investigation of some hofmann-T/sub d/ type complexes: Ni(I-phenyl piperazine)/sub 2/ M(CN)/sub 4/ (M = Cd or Hg)

International Nuclear Information System (INIS)

Parlak, C.; Senyel, M.

2009-01-01

New Hofmann-Td type complexes in the form of Ni(pp)/sub 2/M(CN)/sub 4/ (where pp = 1-Phenyl piperazine and M = Cd or Hg) have been prepared in powder form and their in/Tared (4000-100 cm-l) and Raman (2800-1650 cm/sup -1/) spectra have been reported. The results suggest that these compounds are similar in structure to the Hofmann- T d type complexes, in which the M atom is tetrahedrally coordinated to the carbon atoms of the four cyanide groups, while the Ni atom is octahedrally surrounded by six nitrogen atoms, two of which are from pp ligands which have been coordinated as a un identate ligand coordinating only through the NH nitrogen and the rest are from cyanide groups. In this host structure, the M(CN)/sub 4/ groups have been linked by the Ni(pp)z moieties to form a three-dimensional network. (author)

Compuestos orgánicos persistentes y metales pesados en sangre y efectos en el desarrollo neuropsicológico de la primera infancia en las cohortes de madres-niños INMA (INfancia y Medio Ambiente

Directory of Open Access Journals (Sweden)

Aritz Aranbarri Paredes

2012-08-01

Full Text Available Introducción: El proyecto INMA es un estudio multicéntrico basado en el seguimiento prospectivo de cohortes de madres-hijos en distintas áreas de la geografía española. Objetivo: Estudiar la relación entre los principales contaminantes ambientales y el desarrollo de los niños y niñas en las fases pre y postnatales. Material y Métodos: El conjunto de las cohortes comparten metodología e instrumentos de recogida de información (exposición ambiental, muestras biológicas, exámenes del desarrollo físico y neuropsicológico, cuestionarios de dieta etc. durante el crecimiento intrauterino y en las fases de seguimiento en la infancia. Resultados: Se presentan los niveles de Compuestos Orgánicos Persistentes (COP en suero del primer trimestre de embarazo y de plomo (Pb y mercurio total (Hg-T de cordón umbilical y las asociaciones con el desarrollo neuropsicológico analizadas hasta la fecha. Los COP más frecuentemente encontrados fueron el p,p ́-DDE (99% y el PCB 153 (95% con medias geométricas en suero (ng/g-lípido de 110,0 (p,p ́-DDE y 38,9 (PCB 153. La media geométrica y el nivel máximo de Pb fueron 1,06 μg/dL y 19 μg/dL, respectivamente. La media geométrica de Hg-T fue de 8,2 μg/L, siendo el consumo de pescado el principal predictor. Un 64% de las muestras superan los niveles de referencia de Hg-T establecidos por la USEPA (6,4 μg/L. Conclusión: Los niveles de COP y Pb observados en las áreas de estudio se encuentran en el rango de valores ya descritos en estudios anteriores. Los niveles de Hg requieren una valoración más profunda, así como el estudio de las posibles asociaciones con el desarrollo neuropsicológico. 

Accumulation of Heavy Metals in Crayfish and Fish from Selected Czech Reservoirs

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Iryna Kuklina

2014-01-01

Full Text Available To evaluate the accumulation of aluminium, cadmium, chromium, copper, lead, mercury, nickel, and zinc in crayfish and fish organ tissues, specimens from three drinking water reservoirs (Boskovice, Landštejn, and Nová Říše and one contaminated site (Darkovské moře in the Czech Republic were examined. Crayfish hepatopancreas was confirmed to be the primary accumulating site for the majority of metals (Cu > Zn > Ni > Cd > Cr, while Hg and Cr were concentrated in abdominal muscle, and Al and Pb were concentrated in gill. Metals found in Nová Říše specimens included Cu > Zn > Ni and those found in Boskovice included Zn > Hg > Cr. Cd concentrations were observed only in Landštejn specimens, while contaminated Darkovské moře specimens showed the highest levels of accumulation (Cu > Al > Zn > Pb. The majority of evaluated metals were found in higher concentrations in crayfish: Cu > Al > Zn > Ni > Cr > Cd > Pb, with Hg being the only metal accumulating higher in fish. Due to accumulation similarities of Al in crayfish and fish gill, differences of Hg in muscle, and features noted for the remaining metals in examined tissues, biomonitoring should incorporate both crayfish and fish to produce more relevant water quality surveys.

Speciation, sources, and risk assessment of heavy metals in suburban vegetable garden soil in Xianyang City, Northwest China

Science.gov (United States)

Wang, Lijun; Tao, Wendong; Smardon, Richard C.; Xu, Xue; Lu, Xinwei

2018-06-01

Intensive anthropogenic activities can lead to soil heavy metal contamination resulting in potential risks to the environment and to human health. To reveal the concentrations, speciation, sources, pollution level, and ecological risk of heavy metals in vegetable garden soil, a total of 136 soil samples were collected from three vegetable production fields in the suburbs of Xianyang City, Northwest China. These samples were analyzed by inductively coupled plasma- atomic emission spectrometry and atomic fluorescence spectrometry. The results showed that the mean concentrations of Cd, Co, Cu, Mn, Pb, Zn, and Hg in vegetable garden soil were higher than the corresponding soil element background values of Shaanxi Province. The heavy metals studied in vegetable garden soil were primarily found in the residual fraction, averaging from 31.26% (Pb) to 90.23% (Cr). Considering the non-residual fractions, the mobility or potential risk was in the order of Pb (68.74%)>Co (60.54%)>Mn (59.28%) >Cd (53.54%) ≫Ni (23.36%) >Zn (22.73%)>Cu (14.93%)>V (11.81%)>Cr (9.78%). Cr, Mn, Ni, V, and As in the studied soil were related to soilforming parent materials, while Cu, Hg, Zn, Cd, Co, and Pb were associated with the application of plastic films, fertilizers, and pesticides, as well as traffic emissions and industrial fumes. Cr, Ni, V, and As presented low contamination levels, whereas Co, Cu, Mn, Pb, and Zn levels were moderate, and Cd and Hg were high. Ecological risk was low for Co, Cr, Cu, Mn, Pb, Zn, and As, with high risk observed for Cd and Hg. The overall pollution level and ecological risk of these heavy metals were high.

Speciation, sources, and risk assessment of heavy metals in suburban vegetable garden soil in Xianyang City, Northwest China

Science.gov (United States)

Wang, Lijun; Tao, Wendong; Smardon, Richard C.; Xu, Xue; Lu, Xinwei

2017-07-01

Intensive anthropogenic activities can lead to soil heavy metal contamination resulting in potential risks to the environment and to human health. To reveal the concentrations, speciation, sources, pollution level, and ecological risk of heavy metals in vegetable garden soil, a total of 136 soil samples were collected from three vegetable production fields in the suburbs of Xianyang City, Northwest China. These samples were analyzed by inductively coupled plasma- atomic emission spectrometry and atomic fluorescence spectrometry. The results showed that the mean concentrations of Cd, Co, Cu, Mn, Pb, Zn, and Hg in vegetable garden soil were higher than the corresponding soil element background values of Shaanxi Province. The heavy metals studied in vegetable garden soil were primarily found in the residual fraction, averaging from 31.26% (Pb) to 90.23% (Cr). Considering the non-residual fractions, the mobility or potential risk was in the order of Pb (68.74%)>Co (60.54%)>Mn (59.28%) >Cd (53.54%) ≫Ni (23.36%) >Zn (22.73%)>Cu (14.93%)>V (11.81%)>Cr (9.78%). Cr, Mn, Ni, V, and As in the studied soil were related to soilforming parent materials, while Cu, Hg, Zn, Cd, Co, and Pb were associated with the application of plastic films, fertilizers, and pesticides, as well as traffic emissions and industrial fumes. Cr, Ni, V, and As presented low contamination levels, whereas Co, Cu, Mn, Pb, and Zn levels were moderate, and Cd and Hg were high. Ecological risk was low for Co, Cr, Cu, Mn, Pb, Zn, and As, with high risk observed for Cd and Hg. The overall pollution level and ecological risk of these heavy metals were high.

Analysis of HgI2 and PbI2 crystals and detectors by particle-induced x-ray emission (PIXE) and ion backscattering spectroscopy (IBS)

International Nuclear Information System (INIS)

Bench, G.S.; Heikkinen, D.W.; Antolak, A.J.; Morse, D.H.; Pontau, A.E.; James, R.B.; David, D.C.; Burger, A.; Van Den Berg, L.

1993-03-01

The Ion Micro-Analysis Group (IMAG) in Livermore conducts quantitative trace elemental analysis with PIXE and depth profiling with IBS using an MeV ion microbeam. The system has the capability to produce two-dimensional trace element and IBS images. PIXE analyses have been conducted on HgI 2 and PbI 2 crystals and detector materials in order to identify and quantify near surface trace contaminants. IBS measurements have been conducted to investigate elemental depth distributions in various materials. The results of measurements on several different samples are reported and a discussion of factors affecting quantitative in vacuo microanalysis of these materials is presented

The synthesis and the spectroscopic, thermal, and structural properties of the M2[(fumarate)Ni(CN)4]·2(1,4-Dioxane) clathrate (M = Co, Ni, Cd and Hg)

Science.gov (United States)

Kartal, Zeki; Yavuz, Abdülkerim

2018-03-01

In this study, the clathrates of fumarate-tetracyanonickel-dioxane, given by the formula M2[(fumarate)Ni(CN)4]·2(1,4-Dioxane) (M = Co, Ni, Cd and Hg), have been obtained for the first time through chemical methods. These clathrates have been characterized by elemental, thermal, FT-IR, and FT-Raman spectroscopies. The parameters of structures of clathrates have been determined by X-ray powder diffraction. The thermal behaviors of these clathrates have been also investigated by thermo-gravimetric analysis (TGA), differential thermal analysis (DTA), and derivative thermal gravimetric analysis (DTG) in the range of 20-900 °C. X-ray powder diffraction data have been recorded at ambient temperature in the 2θ range 5-50°. The FT-IR and FT-Raman spectra of clathrates have been recorded in the region of 4000-400 cm-1 and 4000-100 cm-1, respectively. The results of the spectral and thermal analyses of the newly synthesized clathrates of fumarate-tetracyanonickel-dioxane suggest that these clathrates are new examples of the Hofmann-type dioxane clathrates. In our study, the Hofmann-type dioxane clathrates, which are formed by bounding electrons of oxygen-donor atoms of fumarate ion ligand molecule to transition metal atoms, consist of the corrugated |M-Ni(CN)4|∞ polymeric layers, which are held in parallel through the chain of (-M-fumarate-M-).

Determination of heavy metals in chinese prickly ash from different ...

African Journals Online (AJOL)

digestion, and the contents of copper (Cu), nickel (Ni), chromium (Cr), lead (Pb), cadmium ... concentrations of heavy metals in these CPA samples mean they are safe for human consumption. ... poisoning, including Pb, Cd, As, Hg, Sn, and Sb.

Heavy metals pollution and pb isotopic signatures in surface sediments collected from Bohai Bay, North China.

Science.gov (United States)

Gao, Bo; Lu, Jin; Hao, Hong; Yin, Shuhua; Yu, Xiao; Wang, Qiwen; Sun, Ke

2014-01-01

To investigate the characteristics and potential sources of heavy metals pollution, surface sediments collected from Bohai Bay, North China, were analyzed for the selected metals (Cd, Cr, Cu, Ni, Pb, and Zn). The Geoaccumulation Index was used to assess the level of heavy metal pollution. Pb isotopic compositions in sediments were also measured to effectively identify the potential Pb sources. The results showed that the average concentrations of Cd, Cr, Cu, Ni, Pb, and Zn were 0.15, 79.73, 28.70, 36.56, 25.63, and 72.83 mg/kg, respectively. The mean concentrations of the studied metals were slightly higher than the background values. However, the heavy metals concentrations in surface sediments in Bohai Bay were below the other important bays or estuaries in China. The assessment by Geoaccumulation Index indicated that Cr, Zn, and Cd were classified as "the unpolluted" level, while Ni, Cu, and Pb were ranked as "unpolluted to moderately polluted" level. The order of pollution level of heavy metals was: Pb > Ni > Cu > Cr > Zn > Cd. The Pb isotopic ratios in surface sediments varied from 1.159 to 1.185 for (206)Pb/(207)Pb and from 2.456 to 2.482 for (208)Pb/(207)Pb. Compared with Pb isotopic radios in other sources, Pb contaminations in the surface sediments of Bohai Bay may be controlled by the mix process of coal combustion, aerosol particles deposition, and natural sources.

Internal friction of flux motion in Hg-system high-Tc superconductors

International Nuclear Information System (INIS)

Tian, W.; Zhu, J.S.; Shao, H.M.; Li, J.; Wang, Y.N.

1996-01-01

The internal friction(IF) and modulus as functions of temperature were measured for several Hg-system high-Tc superconductors(Hg1201, Hg1223, Hg1223 doped with Fe and Pb), under the applied magnetic field, with vibrating reed technique. An IF peak associated with flux motion can be found below Tc for all samples. The temperature of the IF peak increases with reducing vibrating amplitude. This amplitude dependence of IF indicates that the flux motion is characterized by nonlinear behavior. No apparent shift of IF peak position can be detected by varying the frequency in the range from 10 2 Hz to 10 3 Hz. Furthermore, the IF peak height satisfies a scaling law Q -1 ∝ω -n . This may be originated from phase transition of flux line lattice(FLL) rather than a thermally activated diffusion process. (orig.)

Enhanced Self-Biased Magnetoelectric Coupling in Laser-Annealed Pb(Zr,Ti)O3 Thick Film Deposited on Ni Foil.

Science.gov (United States)

Palneedi, Haribabu; Maurya, Deepam; Geng, Liwei D; Song, Hyun-Cheol; Hwang, Geon-Tae; Peddigari, Mahesh; Annapureddy, Venkateswarlu; Song, Kyung; Oh, Yoon Seok; Yang, Su-Chul; Wang, Yu U; Priya, Shashank; Ryu, Jungho

2018-04-04

Enhanced and self-biased magnetoelectric (ME) coupling is demonstrated in a laminate heterostructure comprising 4 μm-thick Pb(Zr,Ti)O 3 (PZT) film deposited on 50 μm-thick flexible nickel (Ni) foil. A unique fabrication approach, combining room temperature deposition of PZT film by granule spray in vacuum (GSV) process and localized thermal treatment of the film by laser radiation, is utilized. This approach addresses the challenges in integrating ceramic films on metal substrates, which is often limited by the interfacial chemical reactions occurring at high processing temperatures. Laser-induced crystallinity improvement in the PZT thick film led to enhanced dielectric, ferroelectric, and magnetoelectric properties of the PZT/Ni composite. A high self-biased ME response on the order of 3.15 V/cm·Oe was obtained from the laser-annealed PZT/Ni film heterostructure. This value corresponds to a ∼2000% increment from the ME response (0.16 V/cm·Oe) measured from the as-deposited PZT/Ni sample. This result is also one of the highest reported values among similar ME composite systems. The tunability of self-biased ME coupling in PZT/Ni composite has been found to be related to the demagnetization field in Ni, strain mismatch between PZT and Ni, and flexural moment of the laminate structure. The phase-field model provides quantitative insight into these factors and illustrates their contributions toward the observed self-biased ME response. The results present a viable pathway toward designing and integrating ME components for a new generation of miniaturized tunable electronic devices.

Metal transfer to plants grown on a dredged sediment: use of radioactive isotope {sup 203}Hg and titanium

Energy Technology Data Exchange (ETDEWEB)

Caille, Nathalie [ENSAIA-INRA/INPL, 2 avenue de la Foret de Haye, F-54505 Vandoeuvre-les-Nancy (France); CNRSSP, 930 boulevard Lahure, F-59505 Douai (France); Laboratoire des Interactions Microorganismes-Mineraux-Matiere organique dans les sols, CNRS, 17 rue Notre-Dame des Pauvres, F-54505 Vandoeuvre-les-Nancy (France); Vauleon, Clotilde [CNRSSP, 930 boulevard Lahure, F-59505 Douai (France); Leyval, Corinne [Laboratoire des Interactions Microorganismes-Mineraux-Matiere organique dans les sols, CNRS, 17 rue Notre-Dame des Pauvres, F-54505 Vandoeuvre-les-Nancy (France); Morel, Jean-Louis [ENSAIA-INRA/INPL, 2 avenue de la Foret de Haye, F-54505 Vandoeuvre-les-Nancy (France)]. E-mail: jean-louis.Morel@ensaia.inpl-nancy.fr

2005-04-01

Improperly disposed of dredged sediments contaminated with metals may induce long-term leaching and an increase of metal concentrations in ground waters and vegetal cover plants. The objective of the study was to quantify the sediment-to-plant transfer of Cu, Pb, Hg and Zn with a particular focus on the pathway of Hg and to determine whether the establishment of vegetal cover modifies the metal availability. A pot experiment with rape (Brassica napus), cabbage (Brassica oleraccea) and red fescue (Festuca rubra) was set up using a sediment first spiked with the radioisotope {sup 203}Hg. Zinc concentrations (197-543 mg kg{sup -1} DM) in leaves were higher than Cu concentration (197-543 mg kg{sup -1} DM), Pb concentration (2.3-2.6 mg kg{sup -1} DM) and Hg concentration (0.9-1.7 mg kg{sup -1} DM). Leaves-to-sediment ratios decreased as follows: Zn>Cu>Hg>Pb. According to Ti measurements, metal contamination by dry deposition was less than 1%. Mercury concentration in plant leaves was higher than European and French thresholds. Foliar absorption of volatile Hg was a major pathway for Hg contamination with a root absorption of Hg higher in rape than in cabbage and red fescue. Growth of each species increased Cu solubility. Zinc solubility was increased only in the presence of rape. The highest increase of Cu solubility was observed for red fescue whereas this species largely decreased Zn solubility. Dissolved organic carbon (DOC) measurements suggested that Cu solubilisation could result from organic matter or release of natural plant exudates. Dissolved inorganic carbon (DIC) measures suggested that the high Zn solubility in the presence of rape could originate from a generation of acidity in rape rhizosphere and a subsequent dissolution of calcium carbonates. Consequently, emission of volatile Hg from contaminated dredged sediments and also the potential increase of metal solubility by a vegetal cover of grass when used in phytostabilisation must be taken into account

Liquid crystal based optical platform for the detection of Pb2+ ions using NiFe2O4 nanoparticles

Science.gov (United States)

Zehra, Saman; Gul, Iftikhar Hussain; Hussain, Zakir

2018-06-01

A simple, sensitive, selective and real time detection protocol was developed for Pb2+ ions in water using liquid crystals (LCs). In this method, NiFe2O4 nanoparticles were synthesized using chemical co-precipitation method. Crystallite size, morphological, functional groups and magnetization studies were confirmed using X-ray diffraction, Scanning Electron Microscopy, and Fourier transform infrared spectroscopy techniques, respectively. The nanoparticles were mono dispersed with average particle size of 20 ± 2 nm. The surfactant stabilized magnetic nanoparticles were incubated in liquid crystal based sensor system for the detection of Pb+2 ions. The bright to dark transition of LC was observed through optical microscope. When this system was further immersed with a solution containing Pb2+ ions, it caused homeotropic to planar orientation of LC. This interaction is attributed to the presence of abundant hydroxyl groups in such as M-OH, Fe-OH on the surface of spinel ferrites nanoparticles. These groups interact with metal ions at aqueous interface, causing disruption in LCs orientation giving bright texture. This sensor showed higher selectivity towards Pb2+ ions. The detection limit was estimated to be 100 ppb. The cheap and effective protocol reported here should make promising development of LC based sensor for lead ion detection.

Determination of Mn, Fe, Ni, Cu, Zn and Pb contents in samples in samples of apple trees by radionuclide X-ray fluorescence analysis

International Nuclear Information System (INIS)

Bumbalova, A.; Havranek, E.; Harangozo, M.

1982-01-01

The applicability of the radionuclide X-ray fluorescence analysis (RXFA) for qualitative and quantitative evaluation of environmental plant samples is discussed and examples of determination of Mn, Fe, Ni, Cu, Zn, Pb in samples of apple trees are given. The instrumentation, the standard and sample preparation are also presented. (author)

Detection and identification of Cu2+ and Hg2+ based on the cross-reactive fluorescence responses of a dansyl-functionalized film in different solvents.

Science.gov (United States)

Cao, Yuan; Ding, Liping; Wang, Shihuai; Liu, Yuan; Fan, Junmei; Hu, Wenting; Liu, Ping; Fang, Yu

2014-01-08

A dansyl-functionalized fluorescent film sensor was specially designed and prepared by assembling dansyl on a glass plate surface via a long flexible spacer containing oligo(oxyethylene) and amine units. The chemical attachment of dansyl moieties on the surface was verified by contact angle, XPS, and fluorescence measurements. Solvent effect examination revealed that the polarity-sensitivity was retained for the surface-confined dansyl moieties. Fluorescence quenching studies in water declared that the dansyl-functionalized SAM possesses a higher sensitivity towards Hg(2+) and Cu(2+) than the other tested divalent metal ions including Zn(2+), Cd(2+), Co(2+), and Pb(2+). Further measurements of the fluorescence responses of the film towards Cu(2+) and Hg(2+) in three solvents including water, acetonitrile, and THF evidenced that the present film exhibits cross-reactive responses to these two metal ions. The combined signals from the three solvents provide a recognition pattern for both metal ions at a certain concentration and realize the identification between Hg(2+) and Cu(2+). Moreover, using principle component analysis, this method can be extended to identify metal ions that are hard to detect by the film sensor in water such as Co(2+) and Ni(2+).

Identification of the one-quadrupole phonon 21,ms+ state of 204Hg

Directory of Open Access Journals (Sweden)

R. Stegmann

2017-07-01

Full Text Available One-phonon states of vibrational nuclei with mixed proton–neutron symmetry have been observed throughout the nuclear chart besides the mass A≈200 region. Very recently, it has been proposed that the 22+ state of 212Po is of isovector nature. This nucleus has two valence protons and two valence neutrons outside the doubly-magic 208Pb nucleus. The stable isotope 204Hg, featuring two valence-proton and valence-neutron holes, with respect to 208Pb, is the particle-hole mirror of 212Po. In order to compare the properties of low-lying isovector excitations in these particle-hole mirror nuclei, we have studied 204Hg by using the projectile Coulomb-excitation technique. The measured absolute B(M1;22+→21+ strength of 0.20(2μN2 indicates that the 22+ level of 204Hg is at least the main fragment of the 21,ms+ state. For the first time in this mass region, both lowest-lying, one-quadrupole phonon excitations are established together with the complete set of their decay strengths. This allows for a microscopic description of their structures, achieved in the framework of the Quasi-particle Phonon Model.

Human biomonitoring for Cd, Hg and Pb in blood of inhabitants of the Sacco Valley (Italy

Directory of Open Access Journals (Sweden)

Sonia D'Ilio

2013-03-01

Full Text Available INTRODUCTION. The Sacco Valley (Lazio, Italy is characterized by high density population and several industrial chemical productions that during the time had led to a substantial amount of by-products. The result was a severe environmental pollution of the area and in particular of the river Sacco. In 1991, the analysis of water and soils samples of three industrial landfills revealed the presence of organochlorine compounds and heavy metals. A research project named "Health of residents living in Sacco Valley area", coordinated by the regional Department of Epidemiology, was undertaken and financed to evaluate the state of health of the population living near those polluted areas. MATERIALS AND METHODS. Cd, Hg and Pb were quantified in 246 blood samples of potentially exposed residents of the Sacco Valley by quadrupole inductively coupled plasma mass spectrometry (Q-ICP-MS. RESULTS. Individuals who agreed to be sampled did not exhibit high levels of the elements. The distance from the river does not seem to be directly connected with the elements levels in blood. The contribution of these contaminants to the total intake due to ingestion of food was difficult to evaluate. The unclear trend of data would require a characterization of the polluted site with environmental sampling of different matrices.

Ecological risk evaluation of sediment core samples, Lake Tortum (Erzurum, NE Turkey using environmental indices

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Hakan Kaya

2017-11-01

Full Text Available This study aimed to determine the vertical distribution of heavy metals in a 72 cm-long core sample from Lake Tortum in order to shed light on the implications of potential ecological risks. Analysis was based on the use of environmental indices such as the Integrated Pollution Load Index (PLI and Potential Ecological Risk Index (PER. Results reveal that, except for Pb, Mn and Hg, the lowest concentrations of heavy metals occur at a core depth of between 2 cm and 20 cm for Cu, Zn, Ni, Fe, As, Cd, Cr and Al. The highest concentration was found at sampling intervals of 36 cm and 50 cm, with the exception of Pb, Mn, Hg and Ni. The PLI values from bottom to top are less than 1 while the level with the nearest value to the background value lies at a depth between 24 cm and 26 cm. The PER index results suggest a low ecological risk level for Cu, Pb, Zn, Ni, Mn, Fe, As, Cr, and Al; however, Cd and Hg constitute an ecological threat to the lake ecosystem.

Distribution in Portugal of some pollutants in the lichen Parmelia sulcata.

Science.gov (United States)

Freitas, M C; Reis, M A; Alves, L C; Wolterbeek, H T

1999-08-01

During the months of July and August 1993 a lichen (Parmelia sulcata Taylor) collection campaign was held in Portugal where samples were obtained from olive tree bark at 228 sites, following a grid of 10 x 10 km along the Atlantic coast and 50 x 50 km in the interior of the country. The samples were analysed by instrumental neutron activation analysis and proton induced X-ray emission techniques. Concentration data patterns for the pollutants As, Cr, Hg, Ni, Pb, S, Sb, Se, and V were obtained for the whole country surface by making use of an extinction rule of 1/r(3), preventing any cut-off distance from being artificially introduced. Some pollution sources were identified: (1) oil-powered plants on the Lisbon-Setúbal axis (V, Ni), (2) coal-power plants in Porto and Sines (S, Se), (3) traffic in the northern area and the Lisbon-Setúbal axis (Pb), (4) a chemical industry south of Porto (Hg, As), and (5) soil influence (Cr, Sb). Arsenic and chromium results largely exceed, in a few areas, the concentrations acceptable to plants, and in a few spots also Hg, Ni, and Pb data.

Metales pesados (Pb, Cd, Cr y Hg en población general adulta próxima a una planta de tratamiento de residuos urbanos de Bizkaia

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Miren Begoña Zubero Oleagoitia

2008-01-01

Full Text Available Fundamento: Entre las posibles emisiones de una planta de valorización energética de residuos sólidos urbanos (PVERSU se encuentran los metales pesados. el objetivo del estudio es conocer los niveles en sangre y orina de metales pesados en población general de Bizkaia. Métodos: En 2006 se midió la exposición a Pb en 95 muestras de sangre y Cd, Cr y Hg en 93 muestras de orina de adultos de la población general de Bizkaia, País Vasco, obtenidas de dos áreas con alta densidad de tráfico del área metropolitana de Bilbao en la cercanía de una PVERSU que iniciaba su actividad, una tercera correspondiente a una zona urbana de Bilbao con tráfico denso y alejada del área de influencia de las posibles emisiones de la PVERSU y la cuarta alejada de la planta y con baja densidad de tráfico. De cada área se estableció como objetivo elegir a un mínimo 20 participantes, la mitad de cada sexo y, a su vez, la mitad de 20 a 44 años y la mitad de 45 a 69. Se utilizó la prueba de la c2 para estudiar la asociación entre variables categóricas. Como prueba de comparación de medias se utilizó la t de Student y la ANOVA para variables con dos o más categorías, respectivamente. Para ajustar factores de confusión se utilizó un modelo de regresión lineal múltiple. Resultados: Las concentraciones medias fueron PbS: 2,68 ¿g/100ml, CdU 0,54 ug/g creatinina, CrU: 0,51 uig/g creatinina, y HgU: 0,65 ug/g creatinina. Conclusión: No se observaron diferencias entre las zonas. El análisis unifactorial y multifactorial mostró que los niveles de PbS se incrementaban con la edad y estaban asociados con el consumo de productos locales de huerta y con el trabajo en la metalurgia. La edad eleva los niveles de CdU y se observa en clases sociales altas niveles más elevados, así como en mujeres y en personas fumadoras. Los niveles de CrU eran más elevados en zonas alejadas a la PVERSU y en las clases altas. Los niveles de HgU fueron más elevados en

Spatial distribution, ecological and health risk assessment of heavy metals in marine surface sediments and coastal seawaters of fringing coral reefs of the Persian Gulf, Iran.

Science.gov (United States)

Ranjbar Jafarabadi, Ali; Riyahi Bakhtiyari, Alireza; Shadmehri Toosi, Amirhossein; Jadot, Catherine

2017-10-01

Concentrations of 13 heavy metals (Al, Fe, Mn, Zn, Cu, Cr, Co, Ni, V, As, Cd, Hg, Pb) in 360 reef surface sediments (0-5 cm) and coastal seawater samples from ten coral Islands in the Persian Gulf were analyzed to determine their spatial distribution and potential ecological risks. Different sediment quality indices were applied to assess the surface sediment quality. The mean concentrations of metals in studied sediments followed the order: Al > Fe > Ni > V > Mn > Zn > Cu > Cr > Co > As > Cd > Pb > As. Average Cd and Hg exceeded coastal background levels at most sampling sites. With the exception of As, concentrations of heavy metals decreased progressively from the west to the east of the Persian Gulf. Based on the Enrichment Factor (EF) and Potential Ecological Risk Index (RI), concentrations of V, Ni, Hg and Cd indicated moderate contamination and is of some concern. The mean values of heavy metals Toxic Units (TUs) were calculated in the following order: Hg (0.75)> Cr (0.41)> Cd (0.27)> As (0.23)> Cu (0.12)> Zn (0.05)> Pb (0.009). Furthermore, the mean contributing ratios of six heavy metals to Toxic Risk Index (TRI) values were 79% for Hg, 11.48% for Cd, 6.16% for Cr, 3.27% for Cu, 0.07% for Zn and 0.01% for Pb. Calculated values of potential ecological risk factor, revealed that the risk of the heavy metals followed the order Cd > Pb > Ni > Cr > V > Cu > Zn. The results reflected that the level of heavy metals, especially Hg and Cd, are on rise due to emerging oil exploration, industrial development, and oil refineries along the entire Gulf. Fe, Mn, Cu, Zn, V and Ni concentrations in seawater were significantly higher (p heavy metals in the sampling sites. A health risk assessment using the hazard quotient index (HQ) recommended by the USEPA suggests that there is no adverse health effect through dermal exposure, and there is no carcinogenic and non-carcinogenic harm to human health. Copyright © 2017 Elsevier Ltd. All

Synthesis of Pb(II Imprinted Carboxymethyl Chitosan and the Application as Sorbent for Pb(II Ion

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Abu Masykur

2014-07-01

Full Text Available The aims of this research is to synthesize Pb(II imprinted polymers with carboxymethyl chitosan (CMC as polymers and bisphenol A diglycidyl ether (BADGE as cross-linker (Pb-IIP. Chitosan (CTS, non imprinted polymer (NIP and Pb-IIP were characterized using infrared (IR spectroscopy, X-ray diffraction (XRD, surface area analyzer (SAA, scanning electron microscopy (SEM, and energy dispersive X-ray (EDX spectroscopy. The result showed that the adsorption was optimum at pH 5 and contact time of 250 min. Adsorption of Pb(II ion with all of adsorbents followed pseudo-second order kinetic equation. Adsorption of Pb(II ion on CTS followed Freundlich isotherm while that on NIP and Pb-IIP followed the Langmuir adsorption isotherm. The adsorbent of Pb-IIP give higher capacity than the NIP and CTS. Adsorption capacity of Pb-IIP, NIP and CTS were 167.1, 128.9 and 76.1 mg/g, respectively. NIP gave higher adsorption selectivity for Pb(II/Ni(II and Pb(II/Cu(II, whereas Pb-IIP showed higher adsorption selectivity for Pb(II/Cd(II.The hydrogen bonding dominated interaction between Pb(II ion on NIP and Pb-IIP.

Heavy Metals in Soil and Crops of an Intensively Farmed Area: A Case Study in Yucheng City, Shandong Province, China

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Linsheng Yang

2010-02-01

Full Text Available Yucheng City is located in northwestern Shandong Province, China, and is situated on the Huang-Huai-Hai Plain, the largest alluvial plain in China. In this study, 86 surface soil samples were collected in Yucheng City and analyzed for cation exchange capacity (CEC, soil organic matter (SOM, pH, available phosphorus (avail. P, phosphorus (P, aluminum (Al, and iron (Fe. These soils were also analyzed for ‘total’ chromium (Cr, nickel (Ni, copper (Cu, zinc (Zn, arsenic (As, mercury (Hg, cadmium (Cd, and lead (Pb, together with 92 wheat samples and 37 corn samples. There was no obvious heavy metal contamination in the soil and irrigation water. But the long-term accumulation of heavy metals in soil has lead to an increase of Ni, As, Hg and Pb concentrations in some of wheat and corn samples and Cd in wheat samples. Because of the numerous sources of soil heavy metals and the lower level of heavy metal in irrigation water, there is no significant relation between soil heavy metal concentrations and irrigation water concentrations. Cr, Ni were mainly from the indigenous clay minerals according to multivariate analysis. Little contribution to soil heavy metal contents from agricultural fertilizer use was found and the local anomalies of As, Cd, Hg, Pb in wheat and corn grain are attributed to the interactive effects of irrigation and fertilizer used. Aerial Hg, however may also be the source of Hg for soil, wheat and corn.

An ultra-sensitive colorimetric Hg(2+)-sensing assay based on DNAzyme-modified Au NP aggregation, MNPs and an endonuclease.

Science.gov (United States)

Li, Chao; Dai, Peiqing; Rao, Xinyi; Shao, Lin; Cheng, Guifang; He, Pingang; Fang, Yuzhi

2015-01-01

This paper reports the development of an ultra-sensitive colorimetric method for the detection of trace mercury ions involving DNAzymes, Au nanoparticle aggregation, magnetic nanoparticles and an endonuclease. DNAzyme-sensing elements are conjugated to the surface of Au nanoparticle-2, which can crosslink with the T-rich strands coated on Au nanoparticle-1 to form Au nanoparticle aggregation. Other T-rich stands are immobilized on the surface of MNPs. The specific hybridization of these two T-rich strands depends on the presence of Hg(2+), resulting in the formation of a T-Hg(2+)-T structure. Added endonuclease then digests the hybridized strands, and DNAzyme-modified Au NP aggregation is released, catalysing the conversion of the colourless ABTS into a blue-green product by H2O2-mediated oxidation. The increase in the adsorption spectrum of ABTS(+) at 421 nm is related to the concentration of Hg(2+). This assay was validated by detecting mercury ion concentrations in river water. The colorimetric responses were not significantly altered in the presence of 100-fold excesses of other metal ions such as Zn(2+), Pb(2+), Cd(2+), Mn(2+), Ca(2+) and Ni(2+). The inclusion of both Au NP aggregation and an endonuclease enables the assay to eliminate interference from the magnetic nanoparticles with colorimetric detection, decrease the background and improve the detection sensitivity. The calibration curve of the assay was linear over the range of Hg(2+) concentrations from 1 to 30 nM, and the detection limit was 0.8 nM, which is far lower than the 10 nM US EPA limit for drinking water. Copyright © 2014 Elsevier B.V. All rights reserved.

Rhodamine B immobilized on hollow Au-HMS material for naked-eye detection of Hg{sup 2+} in aqueous media

Energy Technology Data Exchange (ETDEWEB)

Zhang, Na [State Key Laboratory of Fine Chemicals, College of Chemical Engineering, Dalian University of Technology, Dalian, 116024 (China); Li, Gang, E-mail: liganghg@dlut.edu.cn [State Key Laboratory of Fine Chemicals, College of Chemical Engineering, Dalian University of Technology, Dalian, 116024 (China); Cheng, Zhuhong [State Key Laboratory of Fine Chemicals, College of Chemical Engineering, Dalian University of Technology, Dalian, 116024 (China); Zuo, Xiujin [Key Laboratory of Bio-organic Chemistry, College of Environmental and Chemical Engineering, Dalian University, Dalian, 116622 (China)

2012-08-30

Graphical abstract: Au-HMS-Probe with worm-like mesoporous framework for detection of Hg{sup 2+} in aqueous media has been simply and effectively synthesized by immobilizing a Rhodamine B derivative on Au-HMS via Au-N groups under room temperature. Highlights: Black-Right-Pointing-Pointer Au-HMS-Probe is prepared via Au-N bonds. Black-Right-Pointing-Pointer Gold nanoparticles are chosen as connectors instead of silane agents. Black-Right-Pointing-Pointer Au-HMS is chosen as carrier for the first time. Black-Right-Pointing-Pointer The immobilization method of Au-HMS-Probe is very simple and effective. Black-Right-Pointing-Pointer Au-HMS-Probe shows excellent ability for detecting Hg{sup 2+} by naked-eye. - Abstract: A simple, effective method has been demonstrated to immobilize Rhodamine B (RhB) probes on mesoporous silica (Au-HMS). The prepared chemosensor (Au-HMS-Probe) was characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray powder diffraction (XRD), UV-vis spectrum and Fourier transform infrared spectroscopy (FT-IR). Further application of Au-HMS-Probe in sensing Hg{sup 2+} was confirmed by fluorescence titration experiment. Au-HMS-Probe afforded 'turn-on' fluorescence enhancement and displayed high brightness in water, and it also showed excellent selectivity for Hg{sup 2+} over alkali (Na{sup +}, K{sup +}), alkaline earth (Mg{sup 2+}, Ca{sup 2+}) and other heavy metal ions (Ag{sup +}, Cd{sup 2+}, Co{sup 2+}, Pb{sup 2+}, Ni{sup 2+}, Cu{sup 2+}, Fe{sup 2+}). Importantly, Au-HMS-Probe could be regenerated by treatment with tetrapropylammonium hydroxide solution.

Stability of binary complexes of Pb(II, Cd(II and Hg(II with maleic acid in TX100-water mixtures

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M. Ramanaiah

2014-09-01

Full Text Available Binary complexes of maleic acid with toxic metal ions such as Pb(II, Cd(II and Hg(II have been studied in 0.0-2.5% v/v tritonX-100 (TX100 - water media at 303 K at an ionic strength of 0.16 M. The active forms of the ligand are LH2, LH- and L2-. The derived ‘best fit’ chemical speciation models are based on crystallographic R-factors, χ2 and Skewness and Kurtosis factors. The predominant species formed are of the type ML2, ML2H and ML3. The trend in variation of complex stability constants with change in the mole fraction of the medium is explained on the basis of prevailing electrostatic and non-electrostatic forces. The species distribution as a function of pH at different compositions of TX100-water mixtures and plausible speciation equilibria are presented and discussed. DOI: http://dx.doi.org/10.4314/bcse.v28i3.7

A metal-organic framework nanocomposite made from functionalized magnetite nanoparticles and HKUST-1 (MOF-199) for preconcentration of Cd(II), Pb(II), and Ni(II)

International Nuclear Information System (INIS)

Ghorbani-Kalhor, Ebrahim

2016-01-01

The author describes the preparation of a magnetic metal organic framework of type MOF-199 containing magnetite (Fe 3 O 4 ) nanoparticles carrying covalently immobilized 4-(thiazolylazo) resorcinol (Fe 3 O 4 -TAR). This material is shown to represent a viable sorbent for separation and preconcentration of Cd(II), Pb(II), and Ni(II) ions. Box-Behnken design was applied to optimize the parameters affecting preconcentration. Following elution with 0.6 mol L −1 EDTA, the ions were quantified by FAAS. The capacity of the sorbent ranged between 185 and 210 mg g −1 . The limits of detection are 0.15, 0.40, and 0.8 ng mL −1 for Cd(II), Ni(II), and Pb(II) ions, respectively. The relative standard deviations are <8.5 %. The method was successfully applied to the rapid extraction of trace amounts of these ions from sea food and agri food. (author)

Liquid crystal based optical platform for the detection of Pb2+ ions using NiFe2O4 nanoparticles

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Saman Zehra

2018-06-01

Full Text Available A simple, sensitive, selective and real time detection protocol was developed for Pb2+ ions in water using liquid crystals (LCs. In this method, NiFe2O4 nanoparticles were synthesized using chemical co-precipitation method. Crystallite size, morphological, functional groups and magnetization studies were confirmed using X-ray diffraction, Scanning Electron Microscopy, and Fourier transform infrared spectroscopy techniques, respectively. The nanoparticles were mono dispersed with average particle size of 20 ± 2 nm. The surfactant stabilized magnetic nanoparticles were incubated in liquid crystal based sensor system for the detection of Pb+2 ions. The bright to dark transition of LC was observed through optical microscope. When this system was further immersed with a solution containing Pb2+ ions, it caused homeotropic to planar orientation of LC. This interaction is attributed to the presence of abundant hydroxyl groups in such as M-OH, Fe-OH on the surface of spinel ferrites nanoparticles. These groups interact with metal ions at aqueous interface, causing disruption in LCs orientation giving bright texture. This sensor showed higher selectivity towards Pb2+ ions. The detection limit was estimated to be 100 ppb. The cheap and effective protocol reported here should make promising development of LC based sensor for lead ion detection. Keywords: Chemical co-precipitation method, Fourier transform infrared spectroscopy, Liquid crystals, Nanoparticles, Sensor, X-ray diffraction

Atomic absorption spectrophotometric determination of microgram levels of Co, Ni, Cu, Pb, and Zn in soil and sediment extracts containing large amounts of Mn and Fe

Science.gov (United States)

Chao, T.T.; Sanzolone, R.F.

1973-01-01

An atomic absorption spectrophotometric method has been developed for the determination of seven metal ions in the hydroxylamine extract of soils and sediments. Mn, Fe, and Zn are directly determined in the aqueous extract upon dilution. Co, Ni, Cu, and Pb in a separate aliquot of the extract are chelated with APDC (ammonium pyrrolidine dithiocarbamate) and extracted into MIBK (methyl isobutyl ketone) before determination. Data are presented to show the quantitative recovery of microgram levels of Co, Ni, Cu, and Pb by APDC-MIBK chelation-extraction from synthetic solutions containing as much as 2,000 ug/ml (micrograms per milliliter) Mn or 50 ug/ml Fe. Recovery of known amounts of the metal ions from sample solutions is equally satisfactory. Reproducible results are obtained by replicate analyses of two sediment samples for the seven metals.

Spectroscopy of 186 Pb with mass identification

International Nuclear Information System (INIS)

Baxter, A.M.; Byrne, A.P.; Australian National Univ., Canberra, ACT; Dracoulis, G.D.; Janssens, R.V.F.; Bearden, I.G.; Henry, R.G.

1993-10-01

Transitions in the very neutron-deficient isotope 186 Pb have been identified in mass-gated, recoil-γ and recoil-γ-γ coincidence data obtained with a Fragment Mass Analyser and Compton-suppressed Ge-detector array. The results of the present work confirm and extend a band of levels tentatively proposed in earlier work done elsewhere, and provide a definitive mass assignment of the observed transitions. The band observed in 186 Pb bears a very close resemblance to the yrast band in the isotones 184 Hg, supporting the view that the 186 Pb band is built upon a prolate structure. 11 refs., 4 figs., 1 tab

Neutron production in bombardments of thin and thick W, Hg, Pb targets by 0.4, 0.8, 1.2, 1.8 and 2.5 GeV protons

International Nuclear Information System (INIS)

Letrourneau, A.; Galin, J.; Goldenbaum, F.; Lott, B.; Peghaire, A.; Enke, M.; Hilscher, D.; Jahnke, U.; Nuenighoff, K.; Filges, D.; Neef, R.D.; Paul, N.; Schaal, H.; Sterzenbach, G.; Tietze, A.

2000-05-01

Neutron experimental data relevant to the design of the target of neutron spallation sources are presented and discussed. The data include the reaction cross sections for W, Hg and Pb investigated with 0.4, 0.8, 1.2, 1.8 and 2.5 GeV proton beams as well as the neutron production, neutron multiplicity distribution, as determined event per event using a high efficiency detector. The production as a function of target material is investigated for both thin (with a single reaction) and thick targets (multiple reactions). Comparisons are made with the predictions of a high energy transport code. (authors)

Recyclable colorimetric sensor of Cr3 + and Pb2 + ions simultaneously using a zwitterionic amino acid modified gold nanoparticles

Science.gov (United States)

Sang, Fuming; Li, Xin; Zhang, Zhizhou; Liu, Jia; Chen, Guofu

2018-03-01

In this work, a rapid, simple and sensitive colorimetric sensor for simultaneous (or respective) detection of Cr3 + and Pb2 + using tyrosine functionalized gold nanoparticles (AuNPsTyr) has been developed. Tyrosine, a natural and zwitterionic amino acid, could be as a reducing and capping agent to synthesise AuNPs and allow for the simultaneous and selective detection of Cr3 + and Pb2 +. Upon the addition of Cr3 + or Pb2 + (a combination of them), the color of AuNPsTyr solution changes from red to blue grey and the characteristic surface plasmon resonance (SPR) band is red-shifted to 580 nm due to the aggregation of AuNPs. Interestingly, the aggregated AuNPsTyr can be regnerated and recycled by removing Pb2 + and Cr3 +. Even after 3 rounds, AuNPsTyr show almost the same A580 nm / A520 nm value for the assays of Pb2 + and Cr3 +, indicating the good recyclability of the colorimetric sensor. The responding time (within 1 min) and sensitivity of the colorimetric sensor are largely improved after the addition of 0.1 M NaCl. Moreover, the AuNPsTyr aggregated by Cr3 + or Pb2 + (a combination of them) show excellent selectivity compared to other metal ions (Cr3 +, Pb2 +, Fe2 +,Cu2 +,Zn2 +,Cr6 +,Ni2 +,Co2 +,Hg2 +,Mn2 +,Mg2 +,Ca2 +,Cd2 +). More importantly, the developed sensor manifests good stability at room temperature for 3 months, which has been successfully used to determine Cr3 + and Pb2 + in the real water samples with a high sensitivity.

Determination of As, Cd, Cu, Hg and Pb in biological samples by modern electrothermal atomic absorption spectrometry

International Nuclear Information System (INIS)

Sardans, Jordi; Montes, Fernando; Penuelas, Josep

2010-01-01

this technique that reaches figures of merit equivalent to Inductively coupled plasma mass spectrometry (ICP-MS). Herein is presented an overview of recent advances and applications of (ETAAS) for the determination of As, Cd, Cu, Hg and Pb in biological samples drawn from studies over the last decade.

Determination of As, Cd, Cu, Hg and Pb in biological samples by modern electrothermal atomic absorption spectrometry

Energy Technology Data Exchange (ETDEWEB)

Sardans, Jordi, E-mail: j.sardans@creaf.uab.ca [Ecophysiological and Global Change Unit CSIC-CREAF, Edifici C, Universitat Autonoma de Barcelona, Bellaterra 08193, Barcelona (Spain); Montes, Fernando [Departamento de Ciencias Analiticas, Facultad de Ciencias, Universidad Nacional de Educacion a Distancia (UNED), C/ Senda del Rey 9. 28040 Madrid (Spain); Penuelas, Josep [Ecophysiological and Global Change Unit CSIC-CREAF, Edifici C, Universitat Autonoma de Barcelona, Bellaterra 08193, Barcelona (Spain)

2010-02-15

of this technique that reaches figures of merit equivalent to Inductively coupled plasma mass spectrometry (ICP-MS). Herein is presented an overview of recent advances and applications of (ETAAS) for the determination of As, Cd, Cu, Hg and Pb in biological samples drawn from studies over the last decade.

Study of multi-nucleon transfer reactions in {sup 58,} {sup 64}Ni + {sup 207}Pb collisions at the velocity filter SHIP

Energy Technology Data Exchange (ETDEWEB)

Comas, V.F.; Heinz, S.; Ackermann, D.; Heredia, J.A.; Hessberger, F.P.; Khuyagbaatar, J.; Kindler, B.; Lommel, B.; Mann, R. [GSI Helmholtzzentrum fuer Schwerionenforschung GmbH, Darmstadt (Germany); Hofmann, S. [GSI Helmholtzzentrum fuer Schwerionenforschung GmbH, Darmstadt (Germany); Goethe-Universitaet Frankfurt, Institut fuer Physik, Frankfurt (Germany)

2013-09-15

We investigated multi-nucleon transfer reactions in collisions of {sup 58}Ni + {sup 207}Pb and {sup 64}Ni + {sup 207}Pb at Coulomb barrier energies. The new aspect is that we used a velocity filter (SHIP at GSI) for the separation of the heavy target-like transfer products from background events. The isotopic identification was performed via the {alpha} decay properties of the reaction products. The goal of the experiment was to study the characteristics of multi-nucleon transfer reactions in the region of heavy nuclei and the applicability of existing separation and detection techniques, which are usually used for identification of heavy fusion-evaporation residues, to heavy transfer products. This was motivated by recent theoretical results from macroscopic-microscopic models which suggest deep inelastic transfer reactions in heavy systems as a means to produce new neutron-rich isotopes in the region of N = 126 and in the region of superheavy nuclei. In this paper we present the isotopic yields, the excitation functions and the excitation energies of the heavy transfer products with Z > 82 as well as the influence of shell effects on the reaction products. The influence of the different neutron numbers of the projectiles is also discussed. (orig.)

A novel starch-based adsorbent for removing toxic Hg(II) and Pb(II) ions from aqueous solution.

Science.gov (United States)

Huang, Li; Xiao, Congming; Chen, Bingxia

2011-08-30

A novel effective starch-based adsorbent was prepared through two common reactions, which included the esterification of starch with excess maleic anhydride in the presence of pyridine and the cross-linking reaction of the obtained macromonomer with acrylic acid by using potassium persulphate as initiator. The percentage of carboxylic groups of the macromonomer ranged from 14% to 33.4%. The cross-linking degree of the adsorbent was tailored with the amount of acrylic acid which varied from 10wt% to 80wt%. Both Fourier transform infrared spectra and thermogravimetric analysis results verified the structure of the adsorbent. The maximum gel fraction and swelling ratio of the adsorbent were about 72% and 6.25, respectively, and they were able to be adjusted with the amount of monomers. The weight loss percentage of the adsorbent could reach 96.9% after immersing in the buffer solution that contained α-amylase for 14h. It was found that the adsorption capacities of the adsorbent for lead and mercury ions could be 123.2 and 131.2mg/g, respectively. In addition, the adsorbent was able to remove ca. 51-90% Pb(II) and Hg(II) ions that existed in the decoctions of four medicinal herbals. Copyright © 2011 Elsevier B.V. All rights reserved.

Century Perspective of Heavy Metal Use in Urban Areas. A Case Study in Stockholm

International Nuclear Information System (INIS)

Soerme, L.; Bergbaeck, B.; Lohm, U.

2001-01-01

The inflow and stock (amount in use) of heavy metals (cadmium(Cd), chromium (Cr), copper (Cu), lead (Pb), mercury (Hg), nickel (Ni) and zinc (Zn)) in goods in 1995 have been quantified in the anthroposphere of Stockholm, Sweden. Statistics on national, regional and local level were used. Contacts were established with representatives from production and construction in the industrial sector and with authorities. The results show that the stock of Cd is 0,2 kg per capita. For the other heavy metals the corresponding result per capita is: Cr 8, Cu 170, Hg 0,01, Ni 4, Pb 73 and Zn 40 kg. The inflow varies between2-8%of the stock indicating the importance of the stock. The lowest levels are for Cu and Pb. Heavy metal levels in solid waste are high, between 15-45% of the amount in the inflow (Hg excluded), the lowest values were for Cu and Pb. Thus, recycling is incomplete. Long life expectancy goods form the majority of the stock but there is a tendency that short life expectancy goods increase their importance in the inflow. Concealed goods are also more frequent in inflow than in the stock

Study of Ni2-Mn-Ga phase formation by magnetron sputtering film deposition at low temperature onto Si substrates and LaNiO3/Pb(Ti,Zr)O3 buffer

International Nuclear Information System (INIS)

Figueiras, F.; Rauwel, E.; Amaral, V. S.; Vyshatko, N.; Kholkin, A. L.; Soyer, C.; Remiens, D.; Shvartsman, V. V.; Borisov, P.; Kleemann, W.

2010-01-01

Film deposition of Ni 2 MnGa phaselike alloy by radio frequency (rf) magnetron sputtering was performed onto bare Si(100) substrates and LaNiO 3 /Pb(Ti,Zr)O 3 (LNO/PZT) ferroelectric buffer layer near room temperature. The prepared samples were characterized using conventional x-ray diffraction (XRD), superconducting quantum interference device, and electron dispersive x-ray spectroscopy from scanning electron microscope observations. The optimized films deposited under high rf power and low argon pressure present good surface quality and highly textured phase crystallization. The positioning distance between the substrate and the target-holder axis has some limited effect on the film's composition due to the specific diffusion behavior of each element in the sputtering plasma. Extended four pole high resolution XRD analysis allowed one to discriminate the intended Ni-Mn-Ga tetragonal martensitic phase induced by the (100) LNO/PZT oriented buffer. This low temperature process appears to be very promising, allowing separate control of the functional layer's properties, while trying to achieve high electromagnetoelastic coupling.

Study of environmental contamination in growth tree rings of Copaifera Langsdorfii by SR-TXRF: evaluation of Cr, Ni, Cu, Zn and Pb

International Nuclear Information System (INIS)

Faria, Bruna Fernanda; Moreira, Silvana; Vives, Ana Elisa S. de

2009-01-01

Some arboreal species present annual cycles of growth and sleeping, registered in the log by different anatomical structures - the growth rings. With the objective of verifying the industrial activity in the city of Bauru, SP samples were submitted to a quantitative analysis in order to verify the bio-accumulation of metals. For that Synchrotron Radiation Total Reflection X-Ray Fluorescence was used. Samples of Copaifera Langsdorfii (Copaiba) were collected close to Municipal Forest of Bauru, SP located at 200m of distance of a disabled company of energy accumulators (batteries) known by receiving several penalties of CETESB due disagreement with the environmental legislation. Through the quantification of the elements Cr, Ni, Cu, Zn and Pb in the annual growth rings were possible to verify the influence of the battery industry in the local pollution. The temporal variation of Pb showed that after the interdiction of the battery industry the concentrations are close to the reference value, but in the periods previous to the industry interdiction the Pb concentrations were above the reference value. For Cr, 46% of the samples presented superior concentration to the reference value. Zinc presented larger concentration in the period from 1996 to 1998, reaching 1383 μg g -1 . For Cu the concentrations were higher than the reference value in almost all periods analyzed, that is, from 1969 to 2004. On the other hand Ni presented great oscillation in its concentration, and the highest values were observed in the period from 1969 to 1971 and from 1999 to 2001, reaching 87 μg g -1 . (author)

Study of environmental contamination in growth tree rings of Copaifera Langsdorfii by SR-TXRF: evaluation of Cr, Ni, Cu, Zn and Pb

Energy Technology Data Exchange (ETDEWEB)

Faria, Bruna Fernanda; Moreira, Silvana, E-mail: bffaria@yahoo.com.b [Universidade Estadual de Campinas (UNICAMP), SP (Brazil). Faculdade de Engenharia Civil, Arquitetura e Urbanismo. Dept. de Saneamento e Ambiente; Vives, Ana Elisa S. de, E-mail: aesvives@unimep.b [Universidade Metodista de Piracicaba (UNIMEP), Santa Barbara D' Oeste, SP (Brazil). Faculdade de Engenharia, Arquitetura e Urbanismo

2009-07-01

Some arboreal species present annual cycles of growth and sleeping, registered in the log by different anatomical structures - the growth rings. With the objective of verifying the industrial activity in the city of Bauru, SP samples were submitted to a quantitative analysis in order to verify the bio-accumulation of metals. For that Synchrotron Radiation Total Reflection X-Ray Fluorescence was used. Samples of Copaifera Langsdorfii (Copaiba) were collected close to Municipal Forest of Bauru, SP located at 200m of distance of a disabled company of energy accumulators (batteries) known by receiving several penalties of CETESB due disagreement with the environmental legislation. Through the quantification of the elements Cr, Ni, Cu, Zn and Pb in the annual growth rings were possible to verify the influence of the battery industry in the local pollution. The temporal variation of Pb showed that after the interdiction of the battery industry the concentrations are close to the reference value, but in the periods previous to the industry interdiction the Pb concentrations were above the reference value. For Cr, 46% of the samples presented superior concentration to the reference value. Zinc presented larger concentration in the period from 1996 to 1998, reaching 1383 mug g{sup -1}. For Cu the concentrations were higher than the reference value in almost all periods analyzed, that is, from 1969 to 2004. On the other hand Ni presented great oscillation in its concentration, and the highest values were observed in the period from 1969 to 1971 and from 1999 to 2001, reaching 87 mug g{sup -1}. (author)

The influence of the shell closure on the microscopic structure of even-even Hg isotopes

International Nuclear Information System (INIS)

Burghardt, A.J.C.

1989-01-01

Muonic X-ray data were obtained for 198 200 202 204 Hg at high-intensity muon-beam facility of SIN and an electron-scattering study was performed on 204 Hg with the 500 MeV, high-resolution electron-scattering facility of NIKHEF-K in a q-range from 0.4 to 2.9 fm -1 . The combined analysis of the elastic electron-scattering and muonic X-ray data has yielded the ground-state charge distribution of 204 Hg. Hartree-Fock calculations with four different interactions, with and without the inclusion of pairing correlations, are compared to this experimental result. The charge-density difference between 206 Pb (determined elsewhere) and 204 Hg is then used ot investigate the filling of the last proton orbit before the Z=82 shell closure, the 3s 1/2 orbit. The interpretation of this difference, also in terms of Hartree-Fock calculations, is discussed in conjunction with the earlier study of Frois et al. concerning 206 Pb and 205 Tl. Many excited states have been observed in the spectra of 204 Hg. The experimental excitation energies and the spins and parities assigned to a number of states are presented. From the cross-section data for these states transition charge distributions have been extracted. Shell-model predictions are compared with the observed level scheme and the shell-model calculation performed by Poppelier is used to interpret transition charge distributions of six states. 101 refs.; 32 figs.; 41 figs

HgSe(Te)-HgHal2 systems

International Nuclear Information System (INIS)

Pan'ko, V.V.; Khudolij, V.A.; Voroshilov, Yu.V.

1989-01-01

Using the methods of differential thermal and X-ray phase analyses the character of chemical interaction in the systems HgTe(Se)-HgHal 2 , where Hal is Cl, Br, I, is investigated. Formation of compounds Hg 3 Se 2 Hal 2 , Hg 3 Te 2 Hal 2 , Hg 3 TeCl 4 and Hg 3 TeBr 4 in these systems is established. The phase diagrams of the studied systems are presented. The parameters of elementary cells of the compounds with the unknown structure, as well as their unknown physicochemical properties, are determined

Application of Zeeman graphite furnace atomic absorption spectrometry with high-frequency modulation polarization for the direct determination of aluminum, beryllium, cadmium, chromium, mercury, manganese, nickel, lead, and thallium in human blood.

Science.gov (United States)

Ivanenko, Natalya B; Solovyev, Nikolay D; Ivanenko, Anatoly A; Ganeev, Alexander A

2012-10-01

Determination of aluminum (Al), beryllium (Be), cadmium (Cd), chromium (Cr), mercury (Hg), manganese (Mn), nickel (Ni), lead (Pb), and thallium (Tl) concentrations in human blood using high-frequency modulation polarization Zeeman graphite furnace atomic absorption spectrometry (GFAAS) was performed. No sample digestion was used in the current study. Blood samples were diluted with deionized water or 0.1 % (m/v) Triton X-100 solution for Tl. Dilution factors ranged from 1/5 per volume for Be and Tl to 1/20 per volume for Cd and Pb. For Tl, Cd, and Hg, noble metals (gold, platinum, rhodium, etc.) were applied as surface modifiers. To mitigate chloride interference, 2 % (m/v) solution of NH(4)NO(3) was used as matrix modifier for Tl and Ni assessment. The use of Pd(NO(3))(2) as oxidative modifier was necessary for blood Hg and Tl measurement. Validation of the methods was performed by analyzing two-level reference material Seronorm. The precision of the designed methods as relative SD was between 4 and 12 % (middle of a dynamic range) depending on the element. For additional validation, spiked blood samples were analyzed. Limits of detection (LoDs, 3σ, n = 10) for undiluted blood samples were 2.0 μg L(-1) for Al, 0.08 μg L(-1) for Be, 0.10 μg L(-1) for Cd, 2.2 μg L(-1) for Cr, 7 μg L(-1) for Hg, 0.4 μg L(-1) for Mn, 2.3 μg L(-1) for Ni, 3.4 μg L(-1) for Pb, and 0.5 μg L(-1) for Tl. The LoDs achieved allowed determination of Al, Cd, Cr, Mn, Ni, and Pb at both toxic and background levels. Be, Hg, and Tl could be reliably measured at toxic levels only. The methods developed are used for clinical diagnostics and biological monitoring of work-related exposure.

Assessing comparative terrestrial ecotoxicity of Cd, Co, Cu, Ni, Pb, and Zn: The influence of aging and emission source

DEFF Research Database (Denmark)

Owsianiak, Mikolaj; Holm, Peter E.; Fantke, Peter

2015-01-01

H or soil organic carbon, emission source occasionally has an effect on reactivity of Cd, Co, Cu, Ni, Pb and Zn emitted from various anthropogenic sources followed by aging in the soil from a few years to two centuries. The uncertainties in estimating the age prevent definitive conclusions about...... the influence of aging time on the reactivity of metals from anthropogenic sources in soils. Thus, for calculating comparative toxicity potentials of man-made metal contaminations in soils, we recommend using time-horizon independent accessibility factors derived from source-specific reactive fractions....

Magnetoelectric coupling and spin-dependent tunneling in Fe/PbTiO3/Fe multiferroic heterostructure with a Ni monolayer inserted at one interface

International Nuclear Information System (INIS)

Dai, Jian-Qing; Zhang, Hu; Song, Yu-Min

2015-01-01

We report on first-principles calculations of a Ni monolayer inserted at one interface in the epitaxial Fe/PbTiO 3 /Fe multiferroic heterostructure, focusing on the magnetoelectric coupling and the spin-dependent transport properties. The results of magnetoelectric coupling calculations reveal an attractive approach to realize cumulative magnetoelectric effects in the ferromagnetic/ferroelectric/ferromagnetic superlattices. The underlying physics is attributed to the combinations of several different magnetoelectric coupling mechanisms such as interface bonding, spin-dependent screening, and different types of magnetic interactions. We also demonstrate that inserting a Ni monolayer at one interface in the Fe/PbTiO 3 /Fe multiferroic tunnel junction is an efficient method to produce considerable tunneling electroresistance effect by modifying the tunnel potential barrier and the interfacial electronic structure. Furthermore, coexistence of tunneling magnetoresistance and tunneling electroresistance leads to the emergence of four distinct resistance states, which can be served as a multistate-storage device. The complicated influencing factors including bulk properties of the ferromagnetic electrodes, decay rates of the evanescent states in the tunnel barrier, and the specific interfacial electronic structure provide us promising opportunities to design novel multiferroic tunnel junctions with excellent performances

Potential use of gypsum and lime rich industrial by-products for induced reduction of Pb, Zn and Ni leachability in an acid soil

International Nuclear Information System (INIS)

Rodriguez-Jorda, M.P.; Garrido, F.; Garcia-Gonzalez, M.T.

2010-01-01

This study evaluates the potential use of four industrial by-products (phosphogypsum (PG), red gypsum (RG), sugar foam (SF), and ashes from biomass combustion (ACB)), applied at two rates in single and combined amendments to reduce the mobility and availability of Pb, Zn and Ni in a metal-spiked acid soil. Leaching experiments were done to estimate leachability indexes and assess their effectiveness. Most of the treatments significantly reduced the metal leachability although only a few were effective for all metals. Based on principal component and cluster analysis, sugar foam (SF) and a mixture of RG and ACB (RG+ACB), both applied at high rate, were selected as first choices to reduce mobility and availability of the three metals. Metal sorption mechanisms involved in the reduction of their leachability were identified using scanning electron microscopy. In the SF-treated samples, the metals were found associated to amorphous Al-hydroxy polymers deposited on phyllosilicates and organic matter particles. In the (RG+ACB)-treated samples, Pb, Zn, and traces of Ni were found associated to Fe/Ti oxide phases with a significant concentration of S, suggesting the formation of metal-sulfate ternary complexes.

Assessment of Metalloid and Metal Contamination in Soils from Hainan, China

Directory of Open Access Journals (Sweden)

Xiangjun Liao

2018-03-01

Full Text Available The characterization of the concentrations and sources of metals and metalloids in soils is necessary to establish quality standards on a regional level and to assess the potential threat of metals to food safety and human health. A total of 8713 soil samples throughout Hainan Island, China were collected at a density of one sample per 4 km2, and concentrations of As, Cd, Cr, Cu, Hg, Ni, Pb, Se, and Zn were analyzed. The geometric mean values of the elements were 2.17, 0.60, 26.5, 9.43, 0.033, 8.74, 22.2, 0.26, and 39.6 mg·· kg−1 for As, Cd, Cr, Cu, Hg, Ni, Pb, Se, and Zn, respectively, significantly lower than the background values of Chinese soils with the exception of Se. Principal component analysis (PCA suggested that multiple anthropogenic sources regulated the elemental compositions of the Hainan environment. Coal combustion and mining are important anthropogenic sources of metals for Hainan. The geochemical maps of elements in Hainan soils were produced using the Geographic Information System (GIS method, and several hot-spot areas were identified. The ecological impact of As, Cd, Cu, Cr, Hg, Pb, Ni, and Zn pollution to the soils was extremely “low”.

Evaluation of the Possible Sources and Controlling Factors of Toxic Metals/Metalloids in the Florida Everglades and Their Potential Risk of Exposure.

Science.gov (United States)

Li, Yanbin; Duan, Zhiwei; Liu, Guangliang; Kalla, Peter; Scheidt, Daniel; Cai, Yong

2015-08-18

The Florida Everglades is an environmentally sensitive wetland ecosystem with a number of threatened and endangered fauna species susceptible to the deterioration of water quality. Several potential toxic metal sources exist in the Everglades, including farming, atmospheric deposition, and human activities in urban areas, causing concerns of potential metal exposure risks. However, little is known about the pollution status of toxic metals/metalloids of potential concern, except for Hg. In this study, eight toxic metals/metalloids (Cd, Cr, Pb, Ni, Cu, Zn, As, and Hg) in Everglades soils were investigated in both dry and wet seasons. Pb, Cr, As, Cu, Cd, and Ni were identified to be above Florida SQGs (sediment quality guidelines) at a number of sampling sites, particularly Pb, which had a level of potential risk to organisms similar to that of Hg. In addition, a method was developed for quantitative source identification and controlling factor elucidation of toxic metals/metalloids by introducing an index, enrichment factor (EF), in the conventional multiple regression analysis. EFs represent the effects of anthropogenic sources on metals/metalloids in soils. Multiple regression analysis showed that Cr and Ni were mainly controlled by anthropogenic loading, whereas soil characteristics, in particular natural organic matter (NOM), played a more important role for Hg, As, Cd, and Zn. NOM may control the distribution of these toxic metals/metalloids by affecting their mobility in soils. For Cu and Pb, the effects of EFs and environmental factors are comparable, suggesting combined effects of loading and soil characteristics. This study is the first comprehensive research with a vast amount of sampling sites on the distribution and potential risks of toxic metals/metalloids in the Everglades. The finding suggests that in addition to Hg other metals/metalloids could also potentially be an environmental problem in this wetland ecosystem.

Geochemical fractionation of Ni, Cu and Pb in the deep sea sediments from the Central Indian Ocean Basin: An insight into the mechanism of metal enrichment in sediment

Digital Repository Service at National Institute of Oceanography (India)

Sensarma, S.; Chakraborty, P.; Banerjee, R.; Mukhopadhyay, S.

speciation study suggests that Fe–Mn oxyhydroxide phase was the major binding phase for Ni, Cu and Pb in the sediments. The second highest concentrations of all these metals were present within the structure of the sediments. Easily reducible oxide phase...

Microanalysis of metals in barbs of a snow petrel (Pagodroma Nivea) from the Antarctica using synchrotron radiation X-ray fluorescence.

Science.gov (United States)

Xie, Zhouqing; Zhang, Pengfei; Sun, Liguang; Xu, Siqi; Huang, Yuying; He, Wei

2008-03-01

For the first time synchrotron radiation X-ray fluorescence (SR-XRF) microanalysis was performed throughout the total length of 4 single barbs from the primaries and secondaries of a snow petrel (Pagodroma Nivea) collected in the Antarctica. Thirteen elements (S, Mg, K, Ca, Fe, Ni, Cu, Zn, Se, Sr, Ba, Hg and Pb) were detected somewhere in the barbs. Variations in levels of these elements within and among the barbs were obvious, indicating nonuniform microscale distributions. Factors influencing the fluctuations of the levels of the elements were investigated using a multivariate statistical analysis method. Five factors (F1 being associated with high loadings of Ca, Sr, and Ni, F2 with high loadings of Fe and Ba, F3 with high loadings of Se and Hg, F4 with high loadings of Ca and K, and F5 with high loadings of Zn and Pb) were found to explain about 80% of the total variance. Results from the factor analysis suggested external contamination of Fe, Ba, Pb, Zn and Hg on the feathers of the snow petrel.

Microanalysis of metals in barbs of a snow petrel (Pagodroma Nivea) from the Antarctica using synchrotron radiation X-ray fluorescence

Energy Technology Data Exchange (ETDEWEB)

Xie Zhouqing [Institute of Polar Environment, School of Earth and Space Sciences, University of Science and Technology of China, Hefei, Anhui 230026 (China)], E-mail: zqxie@ustc.edu.cn; Zhang Pengfei [Department of Earth and Atmospheric Sciences, City College of New York, New York, NY 10031 (United States); Sun Liguang; Xu Siqi [Institute of Polar Environment, School of Earth and Space Sciences, University of Science and Technology of China, Hefei, Anhui 230026 (China); Huang Yuying; He Wei [Institute of High Energy Physics, Chinese Academy of Sciences, 100039 Beijing (China)

2008-03-15

For the first time synchrotron radiation X-ray fluorescence (SR-XRF) microanalysis was performed throughout the total length of 4 single barbs from the primaries and secondaries of a snow petrel (Pagodroma Nivea) collected in the Antarctica. Thirteen elements (S, Mg, K, Ca, Fe, Ni, Cu, Zn, Se, Sr, Ba, Hg and Pb) were detected somewhere in the barbs. Variations in levels of these elements within and among the barbs were obvious, indicating nonuniform microscale distributions. Factors influencing the fluctuations of the levels of the elements were investigated using a multivariate statistical analysis method. Five factors (F1 being associated with high loadings of Ca, Sr, and Ni, F2 with high loadings of Fe and Ba, F3 with high loadings of Se and Hg, F4 with high loadings of Ca and K, and F5 with high loadings of Zn and Pb) were found to explain about 80% of the total variance. Results from the factor analysis suggested external contamination of Fe, Ba, Pb, Zn and Hg on the feathers of the snow petrel.

Microanalysis of metals in barbs of a snow petrel (Pagodroma Nivea) from the Antarctica using synchrotron radiation X-ray fluorescence

International Nuclear Information System (INIS)

Xie Zhouqing; Zhang Pengfei; Sun Liguang; Xu Siqi; Huang Yuying; He Wei

2008-01-01

For the first time synchrotron radiation X-ray fluorescence (SR-XRF) microanalysis was performed throughout the total length of 4 single barbs from the primaries and secondaries of a snow petrel (Pagodroma Nivea) collected in the Antarctica. Thirteen elements (S, Mg, K, Ca, Fe, Ni, Cu, Zn, Se, Sr, Ba, Hg and Pb) were detected somewhere in the barbs. Variations in levels of these elements within and among the barbs were obvious, indicating nonuniform microscale distributions. Factors influencing the fluctuations of the levels of the elements were investigated using a multivariate statistical analysis method. Five factors (F1 being associated with high loadings of Ca, Sr, and Ni, F2 with high loadings of Fe and Ba, F3 with high loadings of Se and Hg, F4 with high loadings of Ca and K, and F5 with high loadings of Zn and Pb) were found to explain about 80% of the total variance. Results from the factor analysis suggested external contamination of Fe, Ba, Pb, Zn and Hg on the feathers of the snow petrel

Assessment of heavy metal pollution, distribution and source apportionment in the sediment from Feni River estuary, Bangladesh.

Science.gov (United States)

Islam, Md Saiful; Hossain, M Belal; Matin, Abdul; Islam Sarker, Md Shafiqul

2018-07-01

Heavy metal pollution in sediment resources may pose serious threat to ecosystem and human health through food web. In this study, surface sediment samples of 10 stations along the Feni River estuary were analyzed to profile the accumulation, sources and pollution levels of heavy metals. The results revealed that the average contents (μg g -1 ) of eight selected heavy metals followed the order of Mn (37.85) > Cr (35.28) > Ni (33.27) > Co (31.02) > Pb (6.47) > Ag (1.09) > As (0.85) > Hg (0.71), and the concentrations varied spatially and seasonally with relatively higher levels at upward stations and during the rainy season. According to sediment quality guidelines (SQGs), the sediment samples were heavily contaminated with Ag and Hg, and moderately with Co. Threshold effect concentration (TEC) and probable effect concentration (PEC) values indicated that the concentration of only Ni and Cr were likely to occasionally exhibit adverse effects on the ecosystem. Enrichment factor (EF), geo-accumulation index (I geo ) and contamination factor (CF) analyses revealed that Ag, Co and Hg were at moderate to high pollution levels and the rests (As, Cr, Ni, Pb and Mn) were at no to low pollution levels. Potential ecological risk index (PERI) also showed that Ag, Co and Hg were the most potential ecological risk factor being determined in this studied area. Correlation matrix combined with multivariate principal component analysis and cluster analysis suggest that Ag, Co, Ni and Hg originated from anthropogenic sources (agrochemicals, silver nanoparticles anti-microbial agent, silver plating), whereas As, Cr, Pb and Mn primarily originated from natural geological background. Copyright © 2018 Elsevier Ltd. All rights reserved.

First principles study of (Cd, Hg, In, Tl, Sn, Pb, As, Sb, Bi, Se) modified Pt(111), Pt(100) and Pt(211) electrodes as CO oxidation catalysts

DEFF Research Database (Denmark)

Tripkovic, Vladimir

2015-01-01

. The coverage dependence as a function of potential for ten different adatom species (Cd, Hg, In, Tl, Sn, Pb, As, Sb, Bi, Se) on bare and CO saturated Pt(111), Pt(100) and Pt(211) surfaces has been established by means of Density Functional Theory calculations. Most of the adatoms are very stable under standard......, given by the OH formation potentials from water, is dependent on the oxophilicity of the adatoms, and is found to scale almost inversely with the adatom stability. In electrolyte solutions saturated with CO, the stability reduces to roughly half of that on bare Pt surfaces. Irrespective of the CO...

210Pb and compositional data of sediments from Rondonian lakes, Madeira River basin, Brazil

International Nuclear Information System (INIS)

Bonotto, Daniel Marcos; Vergotti, Marcelo

2015-01-01

Gold exploration has been intensive in Brazilian Amazon over the last 40 years, where the use of mercury as an amalgam has caused abnormal Hg concentrations in water bodies. Special attention has been directed to Madeira River due to fact it is a major tributary of Amazon River and that since 1986, gold exploration has been officially permitted along a 350 km sector of the river. The 210 Pb method has been used to date sediments taken from nine lakes situated in Madeira River basin, Rondônia State, and to verify where anthropogenic Hg might exist due to gold exploitation in Madeira River. Activity profiles of excess 210 Pb determined in the sediment cores provided a means to evaluate the sedimentation rates using a Constant Flux: Constant Sedimentation (CF:CS) and Constant Rate of Supply (CRS) of unsupported/excess 210 Pb models. A significant relationship was found between the CF:CS sedimentation rates and the mean values of the CRS sedimentation rates (Pearson correlation coefficient r=0.59). Chemical data were also determined in the sediments for identifying possible relationships with Hg occurring in the area. Significant values were found in statistical correlation tests realized among the Hg, major oxides and Total Organic Carbon (TOC) content in the sediments. The TOC increased in the sediment cores accompanied by a loss on ignition (LOI) increment, whereas silica decreased following a specific surface area raising associated to the TOC increase. The CRS model always provided ages within the permitted range of the 210 Pb-method in the studied lakes, whereas the CF:CS model predicted two values above 140 years. - Highlights: • Gold mining activities. • Madeira River basin at Amazon area. • Pb-210 chronological method. • Models for evaluating sedimentation rates

Biosorption of Cd(II), Ni(II) and Pb(II) from aqueous solution by dried biomass of aspergillus niger: application of response surface methodology to the optimization of process parameters

Energy Technology Data Exchange (ETDEWEB)

Amini, Malihe; Younesi, Habibollah [Department of Environmental Science, Faculty of Natural Resources and Marine Sciences, Tarbiat Modares University, Noor (Iran)

2009-10-15

In this study, the biosorption of Cd(II), Ni(II) and Pb(II) on Aspergillus niger in a batch system was investigated, and optimal condition determined by means of central composite design (CCD) under response surface methodology (RSM). Biomass inactivated by heat and pretreated by alkali solution was used in the determination of optimal conditions. The effect of initial solution pH, biomass dose and initial ion concentration on the removal efficiency of metal ions by A. niger was optimized using a design of experiment (DOE) method. Experimental results indicated that the optimal conditions for biosorption were 5.22 g/L, 89.93 mg/L and 6.01 for biomass dose, initial ion concentration and solution pH, respectively. Enhancement of metal biosorption capacity of the dried biomass by pretreatment with sodium hydroxide was observed. Maximal removal efficiencies for Cd(II), Ni(III) and Pb(II) ions of 98, 80 and 99% were achieved, respectively. The biosorption capacity of A. niger biomass obtained for Cd(II), Ni(II) and Pb(II) ions was 2.2, 1.6 and 4.7 mg/g, respectively. According to these observations the fungal biomass of A. niger is a suitable biosorbent for the removal of heavy metals from aqueous solutions. Multiple response optimization was applied to the experimental data to discover the optimal conditions for a set of responses, simultaneously, by using a desirability function. (Abstract Copyright [2009], Wiley Periodicals, Inc.)

Distribution and speciation of heavy metals in sediments from the mainstream, tributaries, and lakes of the Yangtze River catchment of Wuhan, China

International Nuclear Information System (INIS)

Yang Zhifeng; Wang Ying; Shen Zhenyao; Niu Junfeng; Tang Zhenwu

2009-01-01

A comparative study of the heavy metal (As, Cd, Cr, Cu, Hg, Ni, Pb, and Zn) concentrations in sediments collected from the mainstream, tributaries, and lakes of the Yangtze River catchment of Wuhan, China, was conducted. Compared with the maximum background values in Wuhan Province soils, Cd was the metal with the highest contamination level, especially in the mainstream, followed by Zn and Cu. In a few samples from tributaries and lakes, the Hg concentration was very high compared to background levels. The concentrations of As and Ni in all sites fluctuated close to background levels. Partitioning of speciation of each heavy metal in sediments was similar for samples taken from the mainstream, tributaries, and lakes. Compared to the other metals studied, Cd, Cu, Zn, and Pb had higher bioavailability in the three zones, which means they pose a higher ecological risk. Significant correlations among group a (Zn, Cu, and Pb, r > 0.9) and group b (Cr and Ni, r = 0.978) in the mainstream; Hg, Cu, Cd, and Pb in lakes (r > 0.9); and Cu and Pb (r > 0.9) in tributaries were observed using Cluster and correlation analysis. However, a low correlation between As and the other elements in the three zones was shown. Overall, 63.6% of samples from the mainstream, 75.0% from tributaries, and 88.9% from lakes exhibited low and moderate ecological risk of heavy metals, and the potential ecological risks in the mainstream and tributaries were higher than those in lakes.

The behaviour of the elements Ni, Co, Cu, Pb, Zn, Au, Ag, Mo, Sn, W and U in the magmatic, hydrothermal, sedimentary and weathering environments

International Nuclear Information System (INIS)

Anderson, J.R.

1978-01-01

In the last two decades much has been published on the behaviour of certain elements in the magmatic, hydrothermal, sedimentary and weathering environments, but the information is scattered throughout the literature. This situation prompted the present study on the elements Ni, Co, Cu, Pb, Zn, Au, Ag, Mo, Sn, W and U. The behaviour of the elements Ni, Cu, Pb, Zn, Au, Sn, W and U has been studied experimentally in some depth. Ag has been moderately studied, but there is very little information about Co and Mo. Studies on the complexes formed by the elements within the hydrothermal and aqueous environment are often inconclusive and controversial, but conclusions are drawn as to the more likely complexes formed. A genetic classification of ore deposits is used as a framework for the discussion. The source of the elements is regarded as being the mantle, and therefore discussion on other possible sources is beyond the scope of this dissertation. The crystal chemistry and geochemistry of the elements are presented and the essay concludes with a discussion on the elements within their depositional environments

Adsorption of Pb(II), Cu(II), Cd(II), Zn(II), Ni(II), Fe(II), and As(V) on bacterially produced metal sulfides.

Science.gov (United States)

Jong, Tony; Parry, David L

2004-07-01

The adsorption of Pb(II), Cu(II), Cd(II), Zn(II), Ni(II), Fe(II) and As(V) onto bacterially produced metal sulfide (BPMS) material was investigated using a batch equilibrium method. It was found that the sulfide material had adsorptive properties comparable with those of other adsorbents with respect to the specific uptake of a range of metals and, the levels to which dissolved metal concentrations in solution can be reduced. The percentage of adsorption increased with increasing pH and adsorbent dose, but decreased with increasing initial dissolved metal concentration. The pH of the solution was the most important parameter controlling adsorption of Cd(II), Cu(II), Fe(II), Ni(II), Pb(II), Zn(II), and As(V) by BPMS. The adsorption data were successfully modeled using the Langmuir adsorption isotherm. Desorption experiments showed that the reversibility of adsorption was low, suggesting high-affinity adsorption governed by chemisorption. The mechanism of adsorption for the divalent metals was thought to be the formation of strong, inner-sphere complexes involving surface hydroxyl groups. However, the mechanism for the adsorption of As(V) by BPMS appears to be distinct from that of surface hydroxyl exchange. These results have important implications to the management of metal sulfide sludge produced by bacterial sulfate reduction.

A nanostructured Ni/graphene hybrid for enhanced electrochemical hydrogen storage

International Nuclear Information System (INIS)

Choi, Moon-Hyung; Min, Young-Je; Gwak, Gyeong-Hyeon; Paek, Seung-Min; Oh, Jae-Min

2014-01-01

Highlights: • Graphene oxide(GO) was hybridized with the Ni(OH) 2 . • The Ni(OH) 2 /GO was reduced to Ni/graphene. • XRD, TEM, and X-ray absorption spectroscopy were examined. • The hydrogen storage property of Ni/graphene was significantly enhanced. - Abstract: To fabricate electrochemical hydrogen storage materials with delaminated structure, the graphene oxide (GO) in the ethylene glycol solution was reassembled in the presence of the precursor of Ni nanoparticles, and then, the reassembled hybrid was reduced under hydrogen atmosphere to obtain Ni/graphene hybrid. X-ray diffraction patterns and X-ray absorption spectscopic (XAS) analysis clearly show that Ni nanoparticles in Ni/graphene hybrid maintain its nanosized nature even after hybridization with graphene nanosheet (GNS). According to the TEM analysis, the Ni nanoparticles with an average size of 5.2 nm are homogeneously distributed onto the GNS in such a way that the nanoporous structure with much amount of void spaces could be fabricated. The obtained Ni/GNS exhibits a hydrogen storage capacity of 160 mA h/g, while the specific capacity of the graphene nanosheet was only 21 mA h/g. A flexible delaminated structure of Ni/GNS nanocomposite could provide additional intercalation sites for accommodation of hydrogen, leading to the enhancement of hydrogen storage capacity

Proficiency test Plant 6 - determination of As, Cd, Cu, Hg, Pb, Se and Zn in dry mushroom powder (Suillus bovinus)

International Nuclear Information System (INIS)

Polkowska-Motrenko, H.; Dudek, J.; Chajduk, E.; Sypula, M.; Sadowska-Bratek, M.

2006-01-01

Proficiency testing scheme PLANT 6: Determination of As, Cd, Cu, Hg, Pb, Se and Zn in dry mushroom powder (Suillus bovinus) has been described. The proficiency test has been provided by the Institute of Nuclear Chemistry and Technology (Warsaw) with cooperation with POLLAB-CHEM/EURACHEM-PL and REFMAT Society. Wild mushrooms were collected in the forest in north-west Poland, cleaned, i.e. dust, soil and attached mosses were removed. Mushrooms were cut into smaller parts and air dried in a dryer. Dried mushrooms were milled in a centrifugal mill and sieved. Particles of fraction below 1 mm diameter were collected. Analytical samples of 20 g mass were prepared. The material were then characterized by homogeneity testing and determination of assigned values for concentration of elements in question. The testing samples were sent to the laboratories participating in the proficiency test. The results supplied by the participants were statistically evaluated and the calculated values of z-score and En numbers were used for the evaluation of the participating laboratory competency. (author)

Study of the odd mass transition nuclei: 185Hg, 187Hg, 189Hg and 183Ir

International Nuclear Information System (INIS)

Zerrouki, A.

1979-01-01

The radioactive decay of 185 Tl, 186 Tl, 187 Tl has been studied on the isotope separator Isocele II working on line with the Orsay synchrocyclotron from Au( 3 He,xn) reactions: the emitted α lines have been measured and the main γ lines belonging to the 187 Tl→ 187 Hg decay have been identified. The 185 Hg, 187 Hg, 189 Hg high spin states have been studied using the following (HI,xn) reactions obtained on the Strasbourg MP Tandem: 168 Er( 24 Mg,xn) 187 Hg, 188 Hg, 166 Er( 24 Mg,xn) 185 Hg, 186 Hg, 157 Gd( 32 S,xn) 184 Hg, 185 Hg, 158 Gd( 32 S,5n) 185 Hg and 175 Lu( 19 F,5n) 189 Hg. The excitation functions are indicated and a high spin level scheme of 189 Hg is proposed: it is compared to the 'quasiparticle + triaxial rotor' model predictions. A level scheme of 183 Ir is proposed from the data collected at Isolde II (CERN) by Dr. SCHUCK: it is analysed within the framework of the same theoretical model used above [fr

Evaluation of Atriplex halimus, Medicago lupulina and Portulaca oleracea for phytoremediation of Ni, Pb, and Zn.

Science.gov (United States)

Amer, Nasser; Al Chami, Ziad; Al Bitar, Lina; Mondelli, Donato; Dumontet, Stefano

2013-01-01

Suitable plant species are able to accumulate heavy metals and to produce biomass useful for non-food purposes. In this study, three endemic Mediterranean plant species, Atriplex halimus, Portulaca oleracea and Medicago lupulina were grown hydroponically to assess their potential use in phytoremediation and biomass production. The experiment was carried out in a growth chamber using half strength Hoagland's solutions separately spiked with 5 concentrations of Pb and Zn (5, 10, 25, 50, and 100 mg L(-1)), and 3 concentrations of Ni (1, 2 and 5 mg L(-1)). Shoot and root biomass were determined and analyzed for their metals contents. A. halimus and M. lupulina gave high shoot biomass with relatively low metal translocation to the above ground parts. Metals uptake was a function of both metals and plant species. It is worth noting that M. lupulina was the only tested plant able to grow in treatment Pb50 and to accumulate significant amount of metal in roots. Plant metal uptake efficiency ranked as follows: A. halimus > M. lupulina > P. oleracea. Due to its high biomass production and the relatively high roots metal contents, A. halimus and M. lupulina could be successfully used in phytoremediation, and in phytostabilization, in particular.

Magnetoelectric coupling and spin-dependent tunneling in Fe/PbTiO{sub 3}/Fe multiferroic heterostructure with a Ni monolayer inserted at one interface

Energy Technology Data Exchange (ETDEWEB)

Dai, Jian-Qing, E-mail: djqkust@sina.com; Zhang, Hu; Song, Yu-Min [School of Materials Science and Engineering, Kunming University of Science and Technology, Kunming 650093 (China)

2015-08-07

We report on first-principles calculations of a Ni monolayer inserted at one interface in the epitaxial Fe/PbTiO{sub 3}/Fe multiferroic heterostructure, focusing on the magnetoelectric coupling and the spin-dependent transport properties. The results of magnetoelectric coupling calculations reveal an attractive approach to realize cumulative magnetoelectric effects in the ferromagnetic/ferroelectric/ferromagnetic superlattices. The underlying physics is attributed to the combinations of several different magnetoelectric coupling mechanisms such as interface bonding, spin-dependent screening, and different types of magnetic interactions. We also demonstrate that inserting a Ni monolayer at one interface in the Fe/PbTiO{sub 3}/Fe multiferroic tunnel junction is an efficient method to produce considerable tunneling electroresistance effect by modifying the tunnel potential barrier and the interfacial electronic structure. Furthermore, coexistence of tunneling magnetoresistance and tunneling electroresistance leads to the emergence of four distinct resistance states, which can be served as a multistate-storage device. The complicated influencing factors including bulk properties of the ferromagnetic electrodes, decay rates of the evanescent states in the tunnel barrier, and the specific interfacial electronic structure provide us promising opportunities to design novel multiferroic tunnel junctions with excellent performances.

Bioaccumulation of metals (Cd, Cu, Ni, Pb and Zn) in suspended cultures of blue mussels exposed to different environmental conditions

DEFF Research Database (Denmark)

Maar, Marie; Larsen, Martin Mørk; Tørring, Ditte Bruunshøj

2015-01-01

corresponding to Good Ecological Status (GES) in the European Union Water Framework Directive (WFD) and in future climate change scenarios (higher metal concentrations and higher temperatures). For this purpose, GES is interpreted as good chemical status for the metals using the Environmental Quality Standards...... targets for Cd, Ni and Pb are not protective with respect to marine mussel production and probably should be reduced for marine waters. Climate changes may increase the metal contamination of mussels, but not to any critical level at the relatively unpolluted study sites. In conclusion, WFD targets should...

Study of fusion cross-sections of 16O + 208Pb and 28Si + 208Pb reactions by effective soft-core nucleon-nucleon interaction

International Nuclear Information System (INIS)

Ghodsi, O. N.; Mahmodi, M.; Ariai, J.; O. N. Ghodsi)

2007-01-01

In this paper, the cross-sections of fusion reactions 16 O + 208 Pb, 28 Si + 208 Pb, 40 C + 40 Ca, 40 Ca + 48 Ca, 58 Ni + 58 Ni, and 16 O + 154 Sm at bombarding energies above and near the fusion barrier have been investigated. The fusion cross-sections have been studied by means of the Monte Carlo method and effective soft-core nucleon-nucleon interaction. One adjustable parameter was used in these calculations. This parameter can change the strength and repulsive parts of soft-core potential values. It has to be adjusted, so that the analytical results are in acceptable agreement with the experimental data. In our calculations, we have taken the range of the nucleon-nucleon soft-core interaction to be constant and equal to that of the M3Y-Raid potential. Results show that the higher values for the diffusion parameter in the Woods-Saxon potential obtained from a careful analysis of 16 O + 208 Pb and 28 Si + 208 Pb reactions are due to the many particle effects on the nucleon-nucleon potential. (author)

Study of fusion cross-sections of 16O + 208Pb and 28Si + 208Pb reactions by effective soft-core nucleon-nucleon interaction

Directory of Open Access Journals (Sweden)

Ghodsi Omid N.

2007-01-01

Full Text Available In this paper, the cross-sections of fusion reactions 16O + 208Pb, 28Si + 208Pb, 40C + + 40Ca, 40Ca + 48Ca, 58Ni + 58Ni, and 16O + 154Sm at bombarding energies above and near the fusion barrier have been investigated. The fusion cross-sections have been studied by means of the Monte Carlo method and effective soft-core nucleon-nucleon interaction. One adjustable parameter was used in these calculations. This parameter can change the strength and repulsive parts of soft-core potential values. It has to be adjusted, so that the analytical results are in acceptable agreement with the experimental data. In our calculations, we have taken the range of the nucleon-nucleon soft-core interaction to be constant and equal to that of the M3Y-Raid potential. Results show that the higher values for the diffusion parameter in the Woods-Saxon potential obtained from a careful analysis of 16O + 208Pb and 28Si + 208Pb reactions are due to the many particle effects on the nucleon-nucleon potential.

Removal of Heavy Metals Pb2+, Cu2+, Zn2+, Cd2+, Ni2+, Co2+ and Fe3+ from Aqueous Solutions by using Xanthium Pensylvanicum

Directory of Open Access Journals (Sweden)

Jaber SALEHZADEH

2013-11-01

Full Text Available The hazardous ill effects of heavy metals on the environment and public health is a matter of serious concern. Biosorption is emerging as a sustainable effective technology. Heavy metals in water resources are one of the most important environmental problems of countries. The intensification of industrial activity and environmental stress greatly contributes to the significant rise of heavy metal pollution in water resources making threats on terrestrial and aquatic life. The toxicity of metal pollution is slow and interminable, as these metal ions are non bio-degradable. The adsorption capacity of Xanthium Pensylvanicum towards metal ions such as Pb2+, Cu2+, Zn2+, Cd2+, Ni2+, Co2+ and Fe3+, was studied. The adsorption capacity was performed by batch experiments as a function of process parameters (such as sorption time and pH. Experimental results showed that the removal percentages increasing of metal ions at pH=4, initial concentration of metal ions 10 mg/L, and after 90 min of shaking was: Zn2+ < Cd2+ < Cu2+ < Pb2+ < Ni2+ < Fe3+ < Co2+.

$^{204m}$Pb: A new Probe for TDPAC Experiments in Biology Complementing the Well Established Probes $^{111}$Cd and $^{199m}$Hg

CERN Multimedia

2002-01-01

The short-lived nuclear probes $\\,^{111m}$Cd( t$_{1/2}$ = 49 min) , $^{199m}$Hg ( t$_{1/2}$ = 43 min) , and $^{204m}$Pb( t$_{1/2}$ = 43 min) supplied by ISOLDE are used to study the interaction of metals with biological macromolecules like, e.g., DNA and proteins. The structure and dynamics of metal sites in biomolecules are important in determining the functional efficiency of these macromolecules. Many life processes are based on such interactions. In order to study those metal sites close to physiological conditions a highly sensitive spectroscopic method is required, like Time Differential Perturbed Angular Correlation (TDPAC). Here, a radioactive atom is placed at the site of interest and by correlating the emitted $\\gamma$-quanta in space and on a nanosecond time scale local structural information is provided via the Nuclear Quadrupole Interaction. These investigations will allow a deeper insight into the adaptivity and rigidity of metal sites in the blue copper proteins (electron transfer proteins), th...

Quantitative analysis of heavy metals in water samples of the Chapala lake by X-ray fluorescence analysis

International Nuclear Information System (INIS)

Perez Novara, Ana Ma.

1987-01-01

Seven samples of water from Chapala Lake were sent to the ININ X-Ray Fluorescence Laboratory. The presence of Fe, Ni, Cu, Hg and Pb in general could be observed, The results for Pb and Hg were compared with those obtained by atomic absorption in laboratories at the SARH (Ministry of Agriculture and Hydraulic Resources). Corrections had to be made in order to quantify the amount of mercury. There are good working conditions to perform routine analyses of heavy metals ions in water. (author)

Problems with the dating of sediment core using excess 210Pb in a freshwater system impacted by large scale watershed changes

International Nuclear Information System (INIS)

Baskaran, Mark; Nix, Joe; Kuyper, Clark; Karunakara, N.

2014-01-01

Pb-210 dating of freshwater and coastal sediments have been extensively conducted over the past 40 years for historical pollution reconstruction studies, sediment focusing, sediment accumulation and mixing rate determination. In areas where there is large scale disturbance of sediments and the watershed, the vertical profiles of excess 210 Pb ( 210 Pb xs ) could provide erroneous or less reliable information on sediment accumulation rates. We analyzed one sediment core from Hendrix Lake in southwestern Arkansas for excess 210 Pb and 137 Cs. There is no decrease in excess 210 Pb activity with depth while the 137 Cs profile indicates sharp peak corresponding to 1963 and the 137 Cs penetration depth of 137 Cs corresponds to 1952. The historical data on the accelerated mercury mining during 1931–1944 resulted in large-scale Hg input to this watershed. Using the peak Hg activity as a time marker, the obtained sediment accumulation rates agree well with the 137 Cs-based rates. Four independent evidences (two-marker events based on 137 Cs and two marker events based on Hg mining activity) result in about the same sedimentation rates and thus, we endorse earlier suggestion that 210 Pb profile always needs to be validated with at least one another independent method. We also present a concise discussion on what important factors that can affect the vertical profiles of 210 Pb xs in relatively smaller lakes

Etude d’impact des métaux traces (Hg, Cd, Pb, Cu et Zn) dans les cystes et la biomasse "d’Artemia" exploités dans la saline de Sfax

OpenAIRE

Aloui, N.; Amorri, M.; Choub., L.

2010-01-01

RESUME La saline de Sfax constitue un site potentiel pour l’exploitation et la production de l’Artemia locale. Des quantités importantes d’Artemia sont exploitées chaque année (60 kg de cystes poids sec) et sont utilisées en alimentation larvaire. Afin de démontrer l’impact de divers rejets industriels, agricoles dans cette saline, nous avons procédé à la détermination de quelques métaux traces toxiques : le mercure (Hg), le cadmium (Cd), le plomb (Pb), le cuivre (Cu) et le zinc (Zn) p...

Spatial distribution of heavy metals in sediments from the Gulf of Paria,Trinidad

Directory of Open Access Journals (Sweden)

Wendy Norville

2005-05-01

Full Text Available The Gulf of Paria receives heavy metal input from urban runoff,industrial and agricultural activity, sewage and domestic wastes:both from the west coast and from inland areas of Trinidad.Non-residual concentrations of nine metals,as well as total mercury concentrations,were used to determine spatial distributions of heavy metals in sediments in the Gulf of Paria.Surficial sediment samples were collected at 37 stations,which included the mouths of 11 major rivers that flow into the Gulf of Paria.Stations were sampled twice during the wet season (July 1998 and November/December 1998and twice during the dry season (March 1999 and April 1999.Sediments were analyzed for aluminium (Al,cadmium (Cd,chromium (Cr,copper (Cu,iron (Fe, lead (Pb,manganese (Mn,nickel (Ni,zinc (Znand mercury (Hg.Total Organic Carbon (TOCand grain size analyses were also performed on the sediments.Principal component analysis showed that sediments from river mouths subject to greatest land use and anthropogenic input,were distinct from other sediments in the Gulf of Paria.This was due to higher Pb,Zn,Cu and Hg concentrations (3.53-73.30 µg g-1 ,45.8-313.9 µg g-1 ,8.43-39.71 µg g-1 and 0.03-0.10 µg g-1 ,respectively.Sediments further from the coast were also distinct due to their higher Al,Fe,Cr and Mn concentrations (1.37-3.16 mg g-1 ,9.51-18.91 mg g-1 ,17.22-28.41 µg g-1 and 323.6 -1,564.2 µg g-1 ,respectively.Cd and Pb were higher in the wet season while Ni was higher in the dry season.Pb,Zn,Cu and Hg were correlated with each other and with TOC.Correlation was also observed between Al,Fe,Cr,Mn and Ni.Al,Fe,Cr and Mn were correlated with percentage clay in sediments.The results suggest that Pb,Zn, Cu and Hg are preferentially removed by organic matter,which settles at the river-mouths,while Al,Fe,Cr,Mn, and Ni become associated with clay minerals and are transported away from the coast.El Golfo de Paria recibe metales pesados de zonas urbanas,industriales y agr

Permanent tattoos: evidence of pseudolymphoma in three patients and metal composition of the dyes.

Science.gov (United States)

Cristaudo, Antonio; Forte, Giovanni; Bocca, Beatrice; Petrucci, Francesco; Muscardin, Luca; Trento, Elisabetta; Di Carlo, Aldo

2012-01-01

Tattoo-induced pseudolymphoma is a cutaneous inflammatory response, the pathogenesis of which is still unknown. The objective of the present work was to find a possible causal relationship between pseudolymphomatous reactions on the red areas of tattoos and the metals contained in tattoo pigments and skin biopsies. Three individuals with cutaneous lesions on the red areas of tattoos were observed. Clinical and immunohistochemical examinations of the lesions were performed, and the concentrations of Cd, Co, Cr, Hg, Ni and Pb were measured in pigments and biopsy samples. Pseudolymphomas in the red areas were diagnosed in all three cases; one showed the prevalence of B-lymphocytes, whereas the other two showed a prevalence of T cells with a lichenoid pattern. Patch tests were negative. Corticosteroid therapy was ineffective. Cadmium, Co, Hg and Pb in the pigments were probably present as impurities, whereas Cr and Ni were the main components. Chromium and Ni had the highest concentrations, also in the biopsy samples. Permanent tattoos appear to be unsafe, considering the increasing number of diagnosed pseudolymphomas. It can be excluded that Hg was responsible for the reactions, given that the concentration in the red dyes and biopsies was very low. Significant levels of Cr and Ni should be considered as the causes of possible dermal reactions.

Strong room-temperature ultraviolet to red excitons from inorganic organic-layered perovskites, (MX4 (M=Pb, Sn, Hg; X=I-, Br-)

Science.gov (United States)

Ahmad, Shahab; Prakash, G. Vijaya

2014-01-01

Many varieties of layered inorganic-organic (IO) perovskite of type (MX4 (where R: organic moiety, M: divalent metal, and X: halogen) were successfully fabricated and characterized. X-ray diffraction data suggest that these inorganic and organic structures are alternatively stacked up along c-axis, where inorganic mono layers are of extended corner-shared MX6 octahedra and organic spacers are the bi-layers of organic entities. These layered perovskites show unusual room-temperature exciton absorption and photoluminescence due to the quantum and dielectric confinement-induced enhancement in the exciton binding energies. A wide spectral range of optical exciton tunability (350 to 600 nm) was observed experimentally from systematic compositional variation in (i) divalent metal ions (M=Pb, Sn, Hg), (ii) halides (X=I and Br-), and (iii) organic moieties (R). Specific photoluminescence features are due to the structure of the extended MX42- network and the eventual electronic band structure. The compositionally dependent photoluminescence of these IO hybrids could be useful in various photonic and optoelectronic devices.

Enrichment and sources of trace metals in roadside soils in Shanghai, China: A case study of two urban/rural roads.

Science.gov (United States)

Yan, Geng; Mao, Lingchen; Liu, Shuoxun; Mao, Yu; Ye, Hua; Huang, Tianshu; Li, Feipeng; Chen, Ling

2018-08-01

The road traffic has become one of the main sources of urban pollution and could directly affect roadside soils. To understand the level of contamination and potential sources of trace metals in roadside soils of Shanghai, 10 trace metals (Sb, Cr, Co, Ni, Cu, Cd, Pb, Hg, Mn and Zn) from two urban/rural roads (Hutai Road and Wunign-Caoan Road) were analyzed in this study. Antimony, Ni, Cu, Cd, Pb, Hg and Zn concentrations were higher than that of soil background values of Shanghai, whereas accumulation of Cr, Co and Mn were minimal. Significantly higher Sb, Cd, Pb contents were found in samples from urban areas than those from suburban area, suggesting the impact from urbanization. The concentrations of Sb and Cd in older road (Hutai) were higher than that in younger road (Wunign-Caoan). Multivariate statistical analysis revealed that Sb, Cu, Cd, Pb and Zn were mainly controlled by traffic activities (e.g. brake wear, tire wear, automobile exhaust) with high contamination levels found near traffic-intensive areas; Cr, Co, Ni and Mn derived primarily from soil parent materials; Hg was related to industrial activities. Besides, the enrichment of Sb, Cd, Cu, Pb and Zn showed a decreasing trend with distance to the road edges. According to the enrichment factors (EF s ), 78.5% of Sb, Cu, Cd, Pb and Zn were in moderate or significant pollution, indicating considerable traffic contribution. In particular, recently introduced in automotive technology, accumulation of Sb has been recognized in 42.9% samples of both roads. The accumulation of these traffic-derived metals causes potential negative impact to human health and ecological environment and should be concerned, especially the emerging trace elements like Sb. Copyright © 2018 Elsevier B.V. All rights reserved.

Marine environment status assessment based on macrophytobenthic plants as bio-indicators of heavy metals pollution

International Nuclear Information System (INIS)

Zalewska, Tamara; Danowska, Beata

2017-01-01

The main aim of study was to develop the environmental quality standards (EQS MP ) for selected heavy metals: Pb, Cd, Hg and Ni bioaccumulated in the tissues of marine macrophytobenthic plants: Chara baltica, Cladophora spp., Coccotylus truncatus, Furcellaria lumbricalis, Polysiphonia fucoides, Stuckenia pectinata and Zanichellia palustris, collected in designated areas of the southern Baltic Sea in period 2008–2015. The calculated concentration ratios (CR), which attained very high values: 10 4 L kg −1 for lead, 10 3 L kg −1 for nickel and mercury and even 10 5 L kg −1 for cadmium formed the basis for the determination of EQS MP values. The EQS MP values were: 26 mg kg −1 d.w. for Pb, 33 mg kg −1 d.w. for Cd, 32 mg kg −1 d.w. for Ni and 0.4 mg kg −1 d.w. for Hg. The application of macrophytobenthic plants as bioindicators in marine environment status assessment of certain areas of the Baltic Sea is also described in the paper. - Highlights: • Macrophytobenthic plants were applied as a bioindicators for heavy metals pollution assessment. • The environmental quality standards for Pb, Cd, Ni, Hg in macrophytobenthic plants were evaluated. • The marine environment status assessment method based on bioindicators was proposed.

Long-term leaching from MSWI air-pollution-control residues: Leaching characterization and modeling

DEFF Research Database (Denmark)

Hyks, Jiri; Astrup, Thomas; Christensen, Thomas Højlund

2009-01-01

Long-term leaching of Ca, Fe, Mg, K, Na, S, Al, As, Ba, Cd, Co, Cr, Cu, Hg, Mn, Ni, Pb, Zn, Mo, Sb, Si, Sri, Sr, Ti, V, P, Cl, and dissolved organic carbon from two different municipal solid waste incineration (MSWI) air-pollution-control residues was monitored during 24 months of column percolat......Long-term leaching of Ca, Fe, Mg, K, Na, S, Al, As, Ba, Cd, Co, Cr, Cu, Hg, Mn, Ni, Pb, Zn, Mo, Sb, Si, Sri, Sr, Ti, V, P, Cl, and dissolved organic carbon from two different municipal solid waste incineration (MSWI) air-pollution-control residues was monitored during 24 months of column...... percolation experiments; liquid-to-solid (L/S) ratios of 200-250 L/kg corresponding to more than 10,000 years in a conventional landfill were reached. Less than 2% of the initially present As, Cu, Pb, Zn, Cr, and Sb had leached during the Course of the experiments. Concentrations of Cd, Fe, Mg, Hg, Mn, Ni, Co......, Sn, Ti, and P were generally bellow 1 mu g/L; overall less than 1% of their mass leached. Column leaching data were further used in a two-step geochemical modeling in PHREEQC in order to (i) identify solubility controlling minerals and (ii) evaluate their interactions in a water-percolated column...

Analysis and Tendencies of Metals and POPs in a Sediment Core from the Alvarado Lagoon System (ALS), Veracruz, Mexico.

Science.gov (United States)

Botello, A V; Villanueva, F S; Rivera, R F; Velandia, A L; de la Lanza, G E

2018-03-06

This study focused on dating of a sediment core from the Alvarado Lagoon System, Veracruz, Mexico, calculating the sedimentation rate by using 210 Pb to determine the tendency towards pollution by polycyclic aromatic hydrocarbons, organochlorides, the metals Cd, Cr, Cu, Hg, Ni, Pb, and V, and organic matter content. The activity of total Pb and supported Pb in the samples was 83.1 and 29.5 Bq kg -1 , respectively, whereas the average estimated sedimentation rate was 0.48 ± 0.09 cm per year -1 . The organic matter values exhibited linear behavior throughout the historical profile, with values under 2.5%. Metal concentrations followed the order V > Cr > Ni > Cu > Pb > Hg > Cd. Variations found in Cr, Ni, Pb, and V concentrations are basically due to three meteorological phenomena that hit the region: hurricanes Gladys, Hilda, and Janet in September of 1955. V, Ni, and Hg input comes from anthropogenic and lithogenic sources. The presence of individual polycyclic aromatic hydrocarbons showed no ascending accumulation pattern over time, nor did it show any significant statistical correlation to OM. As for the organochlorine pesticides, 63.61% of the total sum of these compounds were from the ciclodienics family. Concentration of p,p'-DDT was observed only in the earliest profile, from 1929.

Magnetic characteristics of M2FeV3O11 (M = Mg, Zn, Pb, Co, Ni) compounds

Science.gov (United States)

Groń, T.; Blonska-Tabero, A.; Filipek, E.; Stokłosa, Z.; Duda, H.; Sawicki, B.

2018-02-01

The unusual physical characteristics of the multicomponent oxide systems renewed the interest as the potential cathode materials in high-energy cells. Since the earlier magnetic characteristics were not entirely conclusive, we report the results of dc magnetic measurements including higher harmonics of ac magnetic susceptibility of the M2FeV3O11 (M = Mg, Zn, Pb, Co, Ni) compounds. Ferrimagnetic long-range and antiferromagnetic short-range interactions for all compounds under study at low temperatures as well as superparamagnetic-like behavior with the blocking temperature of 29 K and the freezing parameter of 0.013 were observed. These effects are discussed within the framework of superexchange and double exchange magnetic interactions as well as the mixed valence band of iron ions.

Esterase activity in the guinea pig thyroid under normal and pathological conditions (vitamin A deficiency) with special regard to cyst-like structures

DEFF Research Database (Denmark)

Kirkeby, S

1977-01-01

By use of different activators and inhibitors, TOCP(tri-o-cresyl phosphate), PCMB (parachloromercury benzoate), NiCl2, Pb(NO3)2, HgCl2, Hg(NO3)2, eserine and sodium taurocholate, it is shown that the esterase in the cyst cells and in group I cells of the guinea pig thyroid probably are A...

Variation in levels and removal efficiency of heavy and trace metals ...

African Journals Online (AJOL)

The general abundance distribution pattern for metals was Zn > Cu > Pb > Cr > Ni > As > Co > Cd > Hg. The removal efficiency ranged from 1.5% for Hg at Zandvliet WWTP plant during winter to 98.27% for Cu at Athlone WWTP treatment plant during summer. The final effluent concentration for most of the metals were within ...

Removal of metals from landfill leachate by sorption to activated carbon, bone meal and iron fines.

Science.gov (United States)

Modin, Hanna; Persson, Kenneth M; Andersson, Anna; van Praagh, Martijn

2011-05-30

Sorption filters based on granular activated carbon, bone meal and iron fines were tested for their efficiency of removing metals from landfill leachate. Removal of Al, As, Ca, Cd, Co, Cr, Cu, Fe, Hg, Mg, Mn, Mo, Ni, Pb, Sr and Zn were studied in a laboratory scale setup. Activated carbon removed more than 90% of Co, Cr, Cu, Fe, Mn and Ni. Ca, Pb, Sr and Zn were removed but less efficiently. Bone meal removed over 80% of Cr, Fe, Hg, Mn and Sr and 20-80% of Al, Ca, Cu, Mo, Ni, Pb and Zn. Iron fines removed most metals (As, Ca, Co, Cr, Cu, Fe, Mg, Mn, Pb, Sr and Zn) to some extent but less efficiently. All materials released unwanted substances (metals, TOC or nutrients), highlighting the need to study the uptake and release of a large number of compounds, not only the target metals. To remove a wide range of metals using these materials two or more filter materials may need to be combined. Sorption mechanisms for all materials include ion exchange, sorption and precipitation. For iron fines oxidation of Fe(0) seems to be important for metal immobilisation. Copyright © 2011 Elsevier B.V. All rights reserved.

Variation of heavy metals within and among feathers of birds of prey: effects of molt and external contamination

Energy Technology Data Exchange (ETDEWEB)

Dauwe, T.; Bervoets, L.; Pinxten, R.; Blust, R.; Eens, M

2003-08-01

Concentrations of many heavy metals in feathers, except Hg, did not reflect the molting sequence, suggesting external contamination. - In this study we examined the effect of external contamination on the heavy metal (Ag, Al, As, Cd, Co, Cr, Cu, Fe, Hg, Mn, Ni, Pb and Zn) concentration in feathers. We compared the heavy metal content among the 10 primary wing feathers of sparrowhawks (Accipiter nisus), little owls (Athene nocta) and barn owls (Tyto alba) and the variation within the outermost tail feather of sparrowhawks and tawny owls (Strix aluco). The concentration of Hg was significantly higher in feathers molted first, suggesting that levels in feathers reflect levels in the blood during formation. For some other elements (Al, Co, Ni, Pb, Zn) on the other hand, there are strong indications that external contamination may have an important impact on the levels detected in the feathers. This should be taken into account in future monitoring studies.

Quantification of chemical elements in blood of patients affected by multiple sclerosis.

Science.gov (United States)

Forte, Giovanni; Visconti, Andrea; Santucci, Simone; Ghazaryan, Anna; Figà-Talamanca, Lorenzo; Cannoni, Stefania; Bocca, Beatrice; Pino, Anna; Violante, Nicola; Alimonti, Alessandro; Salvetti, Marco; Ristori, Giovanni

2005-01-01

Although some studies suggested a link between exposure to trace elements and development of multiple sclerosis (MS), clear information on their role in the aetiology of MS is still lacking. In this study the concentrations of Al, Ba, Be, Bi, Ca, Cd, Co, Cr, Cu, Fe, Hg, Li, Mg, Mn, Mo, Ni, Pb, Sb, Si, Sn, Sr, Tl, V, W, Zn and Zr were determined in the blood of 60 patients with MS and 60 controls. Quantifications were performed by inductively coupled plasma (ICP) atomic emission spectrometry and sector field ICP mass spectrometry. When the two groups were compared, an increased level of Co, Cu and Ni and a decrement of Be, Fe, Hg, Mg, Mo, Pb and Zn in blood of patients were observed. In addition, the discriminant analysis pointed out that Cu, Be, Hg, Co and Mo were able to discriminate between MS patients and controls (92.5% of cases correctly classified).

Trophodynamics of mercury and other trace elements in a pelagic food chain from the Baltic Sea

International Nuclear Information System (INIS)

Nfon, Erick; Cousins, Ian T.; Jaervinen, Olli; Mukherjee, Arun B.; Verta, Matti; Broman, Dag

2009-01-01

Mercury (Hg) and 13 other trace elements (Al, Ti, V, Cr, Fe, Mn, Co, Ni, Cu, Zn, As, Cd, and Pb) were measured in phytoplankton, zooplankton, mysis and herring in order to examine the trophodynamics in a well-studied pelagic food chain in the Baltic Sea. The fractionation of nitrogen isotopes (δ 15 N) was used to evaluate food web structure and to estimate the extent of trophic biomagnification of the various trace elements. Trophic magnification factors (TMFs) for each trace element were determined from the slope of the regression between trace element concentrations and δ 15 N. Calculated TMFs showed fundamental differences in the trophodynamics of the trace elements in the pelagic food chain studied. Concentrations of Al, Fe, Ni, Zn, Pb and Cd showed statistically significant decreases (TMF 1) in concentration with trophic level i.e. Hg biomagnifies in this Baltic food chain. The estimated TMF for Hg in this food chain was comparable to TMFs observed elsewhere for diverse food chains and locations.

Features of the structural and magnetic properties of Pb(TixZr1–xO3-NiFe1.98Co0.02O4 in the polarized state

Directory of Open Access Journals (Sweden)

Baev Vadim

2017-06-01

Full Text Available Composites with a 90%Pb(TixZr1-xO3-10%NiFe1.98Co0.02O4 composition have been synthesized. It has been established that the polarization of samples resulting from exposure to an electric field for 1 hour of 4 kV/mm in strength at a temperature of 400 K leads to crystal structure deformation. The compression of elementary crystal cells in some areas during polarization of the sample creates conditions suitable for the enhancement of magnetic exchange interactions. It has been found that the polarization process of such compositions leads to increases in specific magnetization and magnetic susceptibility. The analysis of Mössbauer spectra has shown that the polarization of the 90%Pb(TixZr1-xO3-10%NiFe1.98Co0.02O4 composite leads to significant changes in the effective magnetic fields of iron subspectra in various positions.

Risk assessment and source analysis of soil heavy metal pollution from lower reaches of Yellow River irrigation in China.

Science.gov (United States)

Zhang, Pengyan; Qin, Chengzhe; Hong, Xin; Kang, Guohua; Qin, Mingzhou; Yang, Dan; Pang, Bo; Li, Yanyan; He, Jianjian; Dick, Richard P

2018-08-15

The level of concentration of heavy metal in soil is detrimental to soil quality. The Heigangkou-Liuyuankou irrigation area in the lower-reach of Yellow River irrigation, as home to a large population and a major site to agricultural production, is vulnerable to heavy metal pollution. This study examined soil quality in Heigangkou-Liuyuankou irrigation areas of Kaifeng, China. Pollution in soil and potential risks introduced by heavy metal accumulation were assessed using Nemerow, Geoaccumulation, and Hakanson's ecological risk indices. Statistics and Geographic Information Systems (GIS) were used to model and present the spatiotemporal changes of the pollution sources and factors affecting the levels of pollution. The heavy metals found in the sampled soil are Cr, Ni, Cu, Zn, Cd, Pb, As, and Hg. Among them, Cd is more concentrated than the others. The southwestern region of the studied area confronts the most serious heavy metal pollution. There exist spatial disparities of low concentrations of different heavy metals in the study area. Hg and Cd are found to pose the highest potential ecological risks. However, their risk levels are not the same across the study area. Levels concentration of Ni, Cu, Zn, Cd, Pb, As, and Hg in soil are highly correlated. In combination, they post an additional threat to the ecological environment. Transportation, rural settlements, and water bodies are found to be the major sources of Cr, Ni, Cu, Zn, Cd, Pb, and Hg pollution in the soil; among the major sources, transportation is the most significant factor. Copyright © 2018 Elsevier B.V. All rights reserved.

Multielement analysis of Zanthoxylum bungeanum Maxim. essential oil using ICP-MS/MS.

Science.gov (United States)

Fu, Liang; Xie, Hualin; Shi, Shuyun

2018-04-12

The concentrations of trace elements (Cr, Ni, As, Cd, Hg, and Pb) in Zanthoxylum bungeanum Maxim. essential oil (ZBMEO) were determined by inductively coupled plasma tandem mass spectrometry. The ZBMEO sample was directly analyzed after simple dilution with n-hexane. Aiming for a relatively high vapor pressure of n-hexane and its resultant loading on plasma, we used a narrow injector torch and optimized plasma radio frequency power and carrier gas flow to ensure stable operation of the plasma. An optional gas flow of 20% O 2 in Ar was added to the carrier gas to prevent the incomplete combustion of highly concentrated organic carbon in plasma and the deposition of carbon on the sampling and skimmer cone orifices. In tandem mass spectrometry mode, O 2 was added to the collision/reaction cell to eliminate the interferences. The limits of detection for Cr, Ni, As, Cd, Hg, and Pb were 2.26, 1.64, 2.02, 1.35, 1.76, and 0.97 ng L -1 , respectively. After determination of 23 ZBMEO samples from different regions in China, we found that the average concentration ranges of trace elements in the 23 ZBMEO samples were 0.72-6.02 ng g -1 , 0.09-2.87 ng g -1 , 0.21-5.84 ng g -1 , 0.16-2.15 ng g -1 , 0.13-0.92 ng g -1 , and 0.17-0.73 ng g -1 for Cr, Ni, As, Cd, Hg, and Pb, respectively. The trace elements in ZBMEO differed significantly when different extraction technologies were used. The study revealed that the contents of the toxic elements As, Cd, Hg, and Pb were extremely low, and hence they are unlikely to pose a health risk following ZBMEO ingestion. Graphical abstract The working mechanism of sample analysis by ICP-MS/MS.

Analysis of several heavy metals in wild edible mushrooms from regions of China.

Science.gov (United States)

Chen, Xin-Hua; Zhou, Hong-Bo; Qiu, Guan-Zhou

2009-08-01

The metal (Cu, Ni, Cd, Hg, As, Pb) contents in wild edible mushrooms collected from three different sites in China were determined by atomic absorption spectrometry and atomic fluorescence spectrometry. All element concentrations were determined on a dry weight basis. A total of 11 species was studied, five being from the urban area and six from rural areas in China. The As content ranged from 0.44 to 1.48 mg/kg. The highest As content was seen in Macrolepiota crustosa from the urban area, and the lowest in Russula virescens from rural areas. A high Ni concentration (1.35 mg/kg) was found in Calvatia craniiformis from the urban area. The lowest Ni level was 0.11 mg/kg, for the species R. virescens and Cantharellus cibarius. The Cu content ranged from 39.0 to 181.5 mg/kg. The highest Cu content was seen in Agaricus silvaticus and the lowest in C. cibarius. The Pb content ranged from 1.9 to 10.8 mg/kg. The highest Pb value was found in C. craniiformis. The Cd content ranged from 0.4 to 91.8 mg/kg. The highest Cd value was found in M. crustosa. The Hg content ranged from 0.28 to 3.92 mg/kg. The highest Hg level was found in Agaricus species. The levels of the heavy metals Cd, Pb, and Hg in the studied mushroom species from urban area can be considered high. The metal-to-metal correlation analysis supported they were the same source of contamination. High automobile traffic was identified as the most likely source of the contamination. Based upon the present safety standards, consumption of those mushrooms that grow in the polluted urban area should be avoided.

A Case Study of Landfill Leachate Using Coal Bottom Ash for the Removal of Cd2+, Zn2+ and Ni2+

Directory of Open Access Journals (Sweden)

Julia Ayala

2016-11-01

Full Text Available The removal of Cd2+, Zn2+ and Ni2+ by coal bottom ash has been investigated. In single metal system, metal uptake was studied in batch adsorption experiments as a function of pH (2–3, contact time (5–180 min, initial metal concentration (50–400 mg/L, adsorbent concentration (5–40 g/L, particle size, and ionic strength (0–1 M NaCl. Removal percentages of metals ions increased with increasing pH and dosage. Removal efficiency at lower concentrations was greater than at higher values. The maximum amount of metal ion adsorbed in milligrams per gram was 35.4, 35.1 and 34.6 mg/g for Zn2+, Cd2+ and Ni2+, respectively, starting out from an initial solution at pH 3. Simultaneous removal of Zn2+, Cd2+ and Ni2+ ions from ternary systems was also investigated and compared with that from single systems. Cd2+ uptake was significantly affected by the presence of competing ions at pH 2. The results obtained in the tests with landfill leachate showed that bottom ash is effective in simultaneously removing several heavy metals such as Ni, Zn, Cd, As, Mn, Cu, Co, Se, Hg, Ag, and Pb.

(210)Pb and compositional data of sediments from Rondonian lakes, Madeira River basin, Brazil.

Science.gov (United States)

Bonotto, Daniel Marcos; Vergotti, Marcelo

2015-05-01

Gold exploration has been intensive in Brazilian Amazon over the last 40 years, where the use of mercury as an amalgam has caused abnormal Hg concentrations in water bodies. Special attention has been directed to Madeira River due to fact it is a major tributary of Amazon River and that since 1986, gold exploration has been officially permitted along a 350km sector of the river. The (21)(0)Pb method has been used to date sediments taken from nine lakes situated in Madeira River basin, Rondônia State, and to verify where anthropogenic Hg might exist due to gold exploitation in Madeira River. Activity profiles of excess (21)(0)Pb determined in the sediment cores provided a means to evaluate the sedimentation rates using a Constant Flux: Constant Sedimentation (CF:CS) and Constant Rate of Supply (CRS) of unsupported/excess (21)(0)Pb models. A significant relationship was found between the CF:CS sedimentation rates and the mean values of the CRS sedimentation rates (Pearson correlation coefficient r=0.59). Chemical data were also determined in the sediments for identifying possible relationships with Hg occurring in the area. Significant values were found in statistical correlation tests realized among the Hg, major oxides and Total Organic Carbon (TOC) content in the sediments. The TOC increased in the sediment cores accompanied by a loss on ignition (LOI) increment, whereas silica decreased following a specific surface area raising associated to the TOC increase. The CRS model always provided ages within the permitted range of the (21)(0)Pb-method in the studied lakes, whereas the CF:CS model predicted two values above 140 years. Copyright © 2015 Elsevier Ltd. All rights reserved.

Elastic and inelastic {alpha}-scattering cross-sections obtained with the 44 MeV fixed energy Saclay cyclotron on separated targets of {sup 24}Mg, {sup 25}Mg, {sup 26}Mg, {sup 40}Ca, {sup 46}Ti, {sup 48}Ti, {sup 50}Ti, {sup 52}Cr, {sup 54}Fe, {sup 56}Fe, {sup 58}Fe, {sup 58}Ni, {sup 60}Ni, {sup 62}Ni, {sup 64}Ni, {sup 63}Cu, {sup 65}Cu, {sup 64}Zn, {sup 112}Sn, {sup 114}Sn, {sup 116}Sn, {sup 118}Sn, {sup 120}Sn, {sup 122}Sn, {sup 124}Sn and {sup 208}Pb using the Saclay fixed-energy cyclotron; Sections efficaces differentielles elastiques et inelastiques obtenues par diffusion de particules {alpha} de 44 MeV sur des cibles de {sup 24}Mg, {sup 25}Mg, {sup 26}Mg, {sup 40}Ca, {sup 46}Ti, {sup 48}Ti, {sup 50}Ti, {sup 52}Cr, {sup 54}Fe, {sup 56}Fe, {sup 58}Fe, {sup 58}Ni, {sup 60}Ni, {sup 62}Ni, {sup 64}Ni, {sup 63}Cu, {sup 65}Cu, {sup 64}Zn, {sup 112}Sn, {sup 114}Sn, {sup 116}Sn, {sup 118}Sn, {sup 120}Sn, {sup 122}Sn, {sup 124}Sn et {sup 208}Pb au cyclotron a energie fixe de saclay

Energy Technology Data Exchange (ETDEWEB)

Bruge, G [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires. Departement de physique nucleaire, service de physique nucleaire a moyenne energie

1967-01-01

This report contains elastic and inelastic {alpha}-scattering cross-sections obtained with the 44 MeV fixed energy Saclay cyclotron on Mg, Ca, Ti, Cr, Fe, Ni, Co, Zn, Sn and Pb enriched targets. (author) [French] Ce rapport contient les tableaux des sections efficaces differentielles obtenues par diffusion elastique et inelastique des particules {alpha} de 44 MeV, fournies par le cyclotron a energie fixe de Saclay, sur des cibles d'isotopes separes de Mg, Ca, Ti, Cr, Fe, Ni, Co, Zn, Sn et Pb. (auteur)

Spatial distribution of heavy metals in sediments from the Gulf of Paria, Trinidad

International Nuclear Information System (INIS)

Norville, W.

2005-01-01

The Gulf of Paria receives heavy metal input from urban runoff, industrial and agricultural activity, sewage and domestic wastes: both from the west coast and from inland areas of Trinidad. Non-residual concentrations of nine metals, as well as total mercury concentrations, were used to determine spatial distributions of heavy metals in sediments in the Gulf of Paria. Surficial sediment samples were collected at 37 stations, which included the mouths of 11 major rivers that flow into the Gulf of Paria. Stations were sampled twice during the wet season (July 1998 and November/ December 1998) and twice during the dry season (March 1999 and April 1999). Sediments were analyzed for aluminium (Al), cadmium (Cd), chromium (Cr), copper (Cu), iron (Fe), lead (Pb), manganese (Mn), nickel (Ni), zinc (Zn) and mercury (Hg). Total Organic Carbon (TOC) and grain size analyses were also performed on the sediments. Principal component analysis showed that sediments from river mouths subject to greatest land use and anthropogenic input, were distinct from other sediments in the Gulf of Paria. This was due to higher Pb, Zn, Cu and Hg concentrations (3.53-73.30 μ g-', 45.8-313.9 μg g-', 8.43-39.71 μg g' and 0.03-0.10 μg g-', respectively). Sediments further from the coast were also distinct due to their higher Al, Fe, Cr and Mn concentrations (1.37-3.16 mg g-', 9.51-18.91 mg g-',17.22-28.41 μg g-' and 323.6--1,564.2 pg g-', respectively). Cd and Pb were higher in the wet season while Ni was higher in the dry season. Pb, Zn, Cu and Hg were correlated with each other and with TOC. Correlation was also observed between Al, Fe, Cr, Mn and Ni. Al, Fe, Cr and Mn were correlated with percentage clay in sediments. The results suggest that Pb, Zn, Cu and Hg are preferentially removed by organic matter, which settles at the river-mouths, while Al, Fe, Cr, Mn, and Ni become associated with clay minerals and are transported away from the coast.(From the author) [es

Doping of (Bi,Pb)-2223 with metal oxides

International Nuclear Information System (INIS)

Goehring, D.; Vogt, M.; Wischert, W.; Kemmler-Sack, S.

1997-01-01

The effect of doping on formation, superconductivity and pinning forces of (Bi,Pb)-2223 was studied for several dopants. They can be subdivided into promoters (Cu, Mn at low doping level of x=0.1 and Rh) and inhibitors (Mg, Al, Sn, Co, Y, Pd and high substitution levels of Mn and Ni) of the transformation of the precursor material into (Bi,Pb)-2223. According to X-ray diffraction (XRD) studies the incorporation of the dopant into the 2223 lattice is restricted to a very low doping level. Higher dopant concentrations are accompanied by a segregation of secondary phases. These segregations are not effective in the process of creating flux pinning centres. A depression of T c is observed for 2223 materials with the dopants Co, Ni and Pd. (orig.)

Hg0 and HgCl2 Reference Gas Standards: ?NIST Traceability ...

Science.gov (United States)

EPA and NIST have collaborated to establish the necessary procedures for establishing the required NIST traceability of commercially-provided Hg0 and HgCl2 reference generators. This presentation will discuss the approach of a joint EPA/NIST study to accurately quantify the true concentrations of Hg0 and HgCl2 reference gases produced from high quality, NIST-traceable, commercial Hg0 and HgCl2 generators. This presentation will also discuss the availability of HCl and Hg0 compressed reference gas standards as a result of EPA's recently approved Alternative Methods 114 and 118. Gaseous elemental mercury (Hg0) and oxidized mercury (HgCl2) reference standards are integral to the use of mercury continuous emissions monitoring systems (Hg CEMS) for regulatory compliance emissions monitoring. However, a quantitative disparity of approximately 7-10% has been observed between commercial Hg0 and HgCl2 reference gases which currently limits the use of (HgCl2) reference gas standards. Resolving this disparity would enable the expanded use of (HgCl2) reference gas standards for regulatory compliance purposes.

[Calculation of environmental dredging depth of heavy sediments in Zhushan Bay of Taihu Lake metal polluted].

Science.gov (United States)

Jiang, Xia; Wang, Wen-Wen; Wang, Shu-Hang; Jin, Xiang-Can

2012-04-01

Horizontal distribution of heavy metals in surface sediments of Zhushan Bay was investigated, and core sediment samples were collected in the representative area. Core sediments were divided into oxide layer (A), polluted layer (B), upper polluted transition layer(C1), lower polluted transition layer(C2) and normal mud layer(D) from top to bottom. The change of total contents of Cr, Ni, Cu, Zn, As, Cd, Hg, Pb and contents of biological available Cr, Ni, Cu, Zn, As, Cd, Pb with depths were analyzed. Ecological risk assessment of heavy metals in sediments was done by potential ecological risk index method. At last, environmental dredging depth was calculated. The results shows that the contents of Cr, Ni, Cu, Zn, As, Cd, Hg, Pb are 30.56-216.58, 24.07-59.95, 16.71-140.30, 84.31-193.43, 3.39-22.30, 0.37-1.59, 0.00-0.80 and 9.67-99.35 mg x kg(-1), respectively. The average concentrations of Cr, Ni, Cu, Zn, As, Cd, Hg, Pb are 79.74, 37.74, 44.83, 122.39, 10.39, 0.77, 0.14 and 40.08 mg x kg(-1), respectively. Heavy metals in the surface sediments of Zhushan Bay mainly distribute in the west bank and the estuaries of Taige canal, Yincun Port, and Huanshan River,and Cd pollution is relatively serious. There is an accumulative effect of heavy metals in Zhushan Bay, and the contents of biological available metals decrease with depths. Ecological risk grades of Cd in layer A and B are high, and the comprehensive potential ecological risk grades of each layer are in middle or low. The environmental dredging layers are A and B, and the average dredging depth is 0.39 m.

Chalcophile elements Hg, Cd, Pb, As in Lake Umbozero, Murmansk Region, Russia

DEFF Research Database (Denmark)

Dauvalter, V.A.; Kashulin, N.A.; Lehto, J.

2009-01-01

is affected by emissions and effluents from mining and metallurgical enterprises of the Murmansk Region, as well as air pollution of a global character. Surface and near-bottom maxima were found in the distributions of Pb and Cd in the water column. These two maxima appear to be associated with the cyclical...

Methylation of Hg downstream from the Bonanza Hg mine, Oregon

Science.gov (United States)

Gray, John E.; Hines, Mark E.; Krabbenhoft, David P.; Thoms, Bryn

2012-01-01

Speciation of Hg and conversion to methyl-Hg were evaluated in stream sediment, stream water, and aquatic snails collected downstream from the Bonanza Hg mine, Oregon. Total production from the Bonanza mine was >1360t of Hg, during mining from the late 1800s to 1960, ranking it as an intermediate sized Hg mine on an international scale. The primary objective of this study was to evaluate the distribution, transport, and methylation of Hg downstream from a Hg mine in a coastal temperate climatic zone. Data shown here for methyl-Hg, a neurotoxin hazardous to humans, are the first reported for sediment and water from this area. Stream sediment collected from Foster Creek flowing downstream from the Bonanza mine contained elevated Hg concentrations that ranged from 590 to 71,000ng/g, all of which (except the most distal sample) exceeded the probable effect concentration (PEC) of 1060ng/g, the Hg concentration above which harmful effects are likely to be observed in sediment-dwelling organisms. Concentrations of methyl-Hg in stream sediment collected from Foster Creek varied from 11 to 62ng/g and were highly elevated compared to regional baseline concentrations (0.11-0.82ng/g) established in this study. Methyl-Hg concentrations in stream sediment collected in this study showed a significant correlation with total organic C (TOC, R2=0.62), generally indicating increased methyl-Hg formation with increasing TOC in sediment. Isotopic-tracer methods indicated that several samples of Foster Creek sediment exhibited high rates of Hg-methylation. Concentrations of Hg in water collected downstream from the mine varied from 17 to 270ng/L and were also elevated compared to baselines, but all were below the 770ng/L Hg standard recommended by the USEPA to protect against chronic effects to aquatic wildlife. Concentrations of methyl-Hg in the water collected from Foster Creek ranged from 0.17 to 1.8ng/L, which were elevated compared to regional baseline sites upstream and downstream

Method for determination of Fe, Co, Ni, Cu, Zn and Pb in sea water using X-ray fluorescence analysis, after concentration step of these elements by coprecipitation with APDC

International Nuclear Information System (INIS)

Lam, P.; Estevez Alvarez, J.R.; Pupo Gonzalez, I.; Ramirez, M.; Rivera, N.

1998-01-01

In this work an analytical procedure has been applied to the to the determination of Fe, Co, Ni, Cu, Zn y Pb in seawater, that includes a coprecipitation step applied of these metals with APDC. The final analysis is carried out by X-Ray Fluorescence Analysis thin layer absolute method

Accumulation of Heavy Metals in Tea Leaves and Potential Health Risk Assessment: A Case Study from Puan County, Guizhou Province, China

Science.gov (United States)

Yang, Ruidong; Chen, Rong; Peng, Yishu; Wen, Xuefeng; Gao, Lei

2018-01-01

This study features a survey of the concentrations of aluminum (Al) and heavy metals (Mn, Pb, Cd, Hg, As, Cr, Ni, Cu, and Zn) in tea leaves and the corresponding cultivation soils (0–30 cm), carried out in Puan County (Guizhou Province, China). The average concentrations of Al, Mn, Pb, Cd, Hg, As, Cr, Ni, Cu, and Zn in the soil were 106 × 103, 214, 20.9, 0.09, 0.12, 17.5, 121, 27.8, 131.2, and 64 mg·kg−1, respectively. The heavy metals’ pollution indexes in the soil can be ranked as follows: Cu > Cr > Hg > As > Ni > Zn > Pb > Mn > Cd. The soil was moderately polluted by Cu because of the high geochemical background value of Cu in the area. The potential environment risk index (RI) showed that 7.69% out of the total sample sites were within the moderate level. Moreover, the ranges of Al, Mn, Pb, Cd, Hg, As, Cr, Ni, Cu, and Zn concentrations in young tea leaves were 250–660, 194–1130, 0.107–0.400, 0.012–0.092, 0.014–0.085, 0.073–0.456, 0.33–1.26, 6.33–14.90, 14.90–26.10, and 35.8–50.3 mg·kg−1, respectively. While in mature tea leaves, they were 4300–10,400, 536–4610, 0.560–1.265, 0.040–0.087, 0.043–0.089, 0.189–0.453, 0.69–2.91, 3.43–14.20, 6.17–16.25, and 9.1–20.0 mg·kg−1, respectively. Furthermore, the concentrations of Pb, Cu, As, Hg, Cd, and Cr in young tea leaves and mature tea leaves were all lower than the standard limit values (5.0, 30, 2.0, 0.3, 1.0, and 5.0 mg·kg−1 for Pb, Cu, As, Hg, Cd, and Cr, respectively) in China. Besides, the accumulation ability of tea leaves to Mn was the strongest, and the average bioconcentration factor (BCF) of Mn in mature tea leaves was 12.5. In addition, the average target hazard quotients (THQ) were all less than one for the young tea leaves and the average aggregate risk hazard index (HI) to adults was 0.272, indicating that there was not a potential health risk for adults through the consumption of the infusions brewed by young tea leaves. However, for mature tea

Concentration of 12 Metals and Metalloids in the Blood of White Stork (Ciconia ciconia): Basal Values and Influence of Age and Gender.

Science.gov (United States)

Maia, Ana Raquel; Soler-Rodriguez, Francisco; Pérez-López, Marcos

2017-11-01

The white stork (Ciconia ciconia) is being increasingly used in biomonitoring programmes of environmental contaminants due to its growing population in Europe; however, studies on inorganic elements are scarce. The blood of 70 white storks was collected and analysed by inductively coupled plasma mass spectroscopy (ICP-MS) to determine the presence of the following elements: lead (Pb), mercury (Hg), arsenic (As), nickel (Ni), iron (Fe), zinc (Zn), copper (Cu), selenium (Se), manganese (Mn), chromium (Cr), cobalt (Co), and cadmium (Cd). Our main goals were to determine the mean concentrations of these elements in the blood and to study its association with age and gender. Mean concentrations were highest for Fe, followed by Zn, and lowest for Co and Cd. The metal levels were similar to the values referred in the literature for the same species from different locations. No statistically significant differences were found between males and females. Regarding age, statistically significant differences were observed for Ni, Cu, Se, Hg, and Pb between young and adult animals (except for Pb, values in adults were higher than in fledglings). Many element concentrations were correlated, with the strongest correlations between the pairs Hg-Se, Hg-As, and Fe-Zn, mainly in adults. This study provides the baseline data for a monitoring program based on white stork blood as a nondestructive sample.

The Vein-type Zn-(Pb, Cu, As, Hg) mineralization at Fedj Hassene ore field, North-Western Tunisia: Mineralogy, Trace Elements, Sulfur Isotopes and Fluid Inclusions; Le champ filonien a Zn-(Pb, Cu, As, Hg) du district minier de Fedj Hassene (Nord Ouest de la Tunisie): Mineralogie, Elements en traces, Isotopes du Soufre et Inclusions Fluides

Energy Technology Data Exchange (ETDEWEB)

Bejaouil, J.; Bouhlel, S.; Barca, D.; Braham, A.

2011-07-01

The Fedj Hassene district is localized at the edge of the Tuniso-Algerian border 10 km of Ghardimaou area. It consists of a Zn-Pb vein type with minor amounts of Cu-As-Hg. The total Zn reserves are about 370.000t. The mineralization occurs within sub parallel fractures to the Ain El Kohla ESE-WNW fault. Host rocks consist of limestones and marly limestones of the Middle Turonian. In the principal lode of Fedj Hassene, the mineralization occurs as vein filling of massive and brecciated brown sphalerite and minor galena ore with gangue. Other trace minerals are pyrite, chalcopyrite, orpiment, realgar, smithsonite and cerussite. LA-ICP-MS analyses in sphalerites show mean contents of 0,84 wt% Fe, 0,14 wt% Cd and 0,02 wt% Mn Ore. Fluid inclusions study in calcite and sphalerite reveals one mineralizing fluid characterized by an average salinity 23% wt NaCl with decreasing homogenisation temperature. In fact the temperature shows decrease from sphalerite to calcite. The fluid density that corresponds to trapping pressure ranges between 1.00 g/cm{sup 3} and 1.11 g/cm{sup 3} and pressure close to 200 bars. Micro thermometric data in fluid inclusion hosted by gangue mineral presented by calcite show an average temperature of formation around 194 degree centigrade. These inclusions homogenized to the liquid phase between 156 degree centigrade and 210 degree centigrade and salinities values ranging from 22 to 28 wt% NaCl and an average around 23% wt NaCl. The {delta}{sup 3}4S (VCDT) values of sphalerite are in the range of + 4,6% to 6,4% (average=5,6%). Thermochemical reduction of Triassic sulfate by reaction with hydro-carbons is the most probable source for the heavy and the narrow range of the d{delta}{sup 3}4S values. Mineralogical, geochemical of trace elements, fluid inclusions and sulfur isotopes studies allow to include the vein-type ore field of Fedj Hassene in the polymetallic (Pb-Zn-As-Hg) vein mineralization of the nappe zone in northern Tunisia and north eastern

Heavy metals in soils of Hechuan County in the upper Yangtze (SW China): Comparative pollution assessment using multiple indices with high-spatial-resolution sampling.

Science.gov (United States)

Ni, Maofei; Mao, Rong; Jia, Zhongmin; Dong, Ruozhu; Li, Siyue

2018-02-01

In order to assess heavy metals (HMs) in soils of the upper Yangtze Basin, a very high-spatial-resolution sampling (582 soil samples) was conducted from Hechuan County, an important agricultural practice area in the Southwest China. Multiple indices including geoaccumulation index (I geo ), enrichment factor (EF), sediment pollution index (SPI) and risk index (RI), as well as multivariate statistics were employed for pollution assessment and source identification of HMs in soils. Our results demonstrated that the averages of eight HMs decreased in the following order: Zn (82.8 ± 15.9) > Cr (71.6 ± 12.2) > Ni (32.1 ± 9.89) > Pb (27.6 ± 13.8) > Cu (25.9 ± 11.8) > As (5.48 ± 3.42) > Cd (0.30 ± 0.077) > Hg (0.082 ± 0.092). Averages of HMs except Cd were lower than threshold value of Environmental Quality Standard for Soils, while 43% of total samples had Cd concentration exceeding the national standard, 1% of samples for Hg and 5% samples for Ni, moreover, Cd and Hg averages were much higher than their background levels. I geo and EF indicated that their levels decreased as follows: Cd > Hg > Zn > Pb > Ni > Cu > Cr > As, with moderate enrichments of Cd and Hg. RI indicated that 61.7% of all samples showed moderate risk, while 6.5% of samples with greater than considerable risk due to human activities should be paid more attention. Multivariate analysis showed lithogenic source of Cu, Cr, Ni and Zn, while Cd and Hg were largely contributed by anthropogenic activities such as agricultural practices. Our study would be helpful for improving soil environmental quality in SW, China, as well as supplying modern approaches for other areas with soil HM pollution. Copyright © 2017 Elsevier Inc. All rights reserved.

Super(210) Pb based trace element fluxes in the nearshore and estuarine sediments off Bombay, India

Digital Repository Service at National Institute of Oceanography (India)

Sharma, P.; Borole, D.V.; Zingde, M.D.

Seven sediment cores from the Thana Creek-Bombay harbour complex (THC) have been studied for excess super(210) Pb (super(210) Pb sub(exc), that portion of super(210) Pb not supported by decay of super(226) Ra in sediment), C sub(org), Mn, Fe, Co, Ni...

196Hg and 202Hg isotopic ratios in chondrites: revisited

International Nuclear Information System (INIS)

Jovanovic, S.; Reed, G.W. Jr.

1976-01-01

Additional evidence for an isotopically anomalous Hg fraction in unequilibrated meteorites has been obtained using neutron activation to produce 196 Hg and 202 Hg followed by stepwise heating to extract the Hg. In the latest experiments Allende matrix samples released the anomalous Hg but various high-temperature inclusions did not. Nucleogenetic processes are suggested as the probable cause of the anomaly. (Auth.)

Radiation Induced Preparation of Polymer Membranes Grafted with Basic and Acidic Monomers for Application in Wastewater Treatment

Energy Technology Data Exchange (ETDEWEB)

Ajji, Z [Polymer Technology Division, Radiation Technology Department, Atomic Energy Commission of Syria (AECS), 17th Nissan Street, Kafar Sousah, Damascus (Syrian Arab Republic)

2012-09-15

Polymer membranes (PP and PE) had been grafted with basic and acidic functional groups using gamma radiation. Two binary mixtures had been used for the grafting reactions: acrylic acid/N-vinyl pyrrolidone, and acrylic acid/N-vinyl imidazole. The influence of different reaction parameters on the grafting yield had been investigated as: type of solvent and solvent composition, comonomer concentration and composition, addition of inhibitors, and dose. Water uptake with respect to the grafting yield had also been evaluated. The ability of PP films, grafted with acrylic acid/ vinyl pyrrolidone, to uptake heavy metal ions such as Hg{sup 2+}, Pb{sup 2+}, Cd{sup 2+}, Co{sup 2+}, Ni{sup 2+} and Cu{sup 2+} was elaborated. The uptake of the metal ions increases with increasing the grafting yield. Furthermore, the Pb{sup +2} uptake was much higher than the uptake of the Hg{sup 2+} and Cd{sup 2+} ions. The membranes may be considered for the separation of Pb{sup 2+} ions from Hg{sup 2+} or Cd{sup 2+} ions. Also the ability of PE films, grafted with acrylic acid/ N-vinyl imidazole to uptake heavy metal ions such as Pb{sup 2+}, Cd{sup 2+}, Co{sup 2+} and Ni{sup 2+} was elaborated. An increase in the uptake of the metal ions was observed as the grafting yield increased. (author)

Measurements of labile Cd, Cu, Ni, Pb, and Zn levels at a northeastern Brazilian coastal area under the influence of oil production with diffusive gradients in thin films technique (DGT).

Science.gov (United States)

de Souza, João M; Menegário, Amauri A; de Araújo Júnior, Marcus A G; Francioni, Eleine

2014-12-01

In this work, the ability of the diffusive gradients in thin films technique (DGT) was evaluated for monitoring the concentrations, and estimating the availability, of metals at a northeastern Brazilian coastal area under the influence of oil production. Three sites with an average distance between 0m (EM-1), 100 m (EM-2), and 1,000 m (EM-3) of a submarine outfall-I (Guamaré-RN, Brazil) and another site (GA-1) with an average distance of 12,000 m east of Outfall I, near the city of Galinhos, were studied. DGT units were deployed at the same sites in three campaigns from July, 2010 to June, 2011. Effects on the accuracy of analytical results regarding the deployment time, gel porosity, and thickness were evaluated. There was no difference between the measurements obtained with two sets of DGT devices, those assembled with open or restrictive pore gel, respectively, showing that organic metallic species are not present near the submarine outlet. After 21 day deployments in a region (near Submarine Outfall I) that receives produced waters that have been treated, there was evidence of biofilm formation on DGT membranes. However, it was demonstrated that the biofilm interference with DGT measurements was negligible. Data found in this work show that total concentrations of Cd, Cu, Pb, Ni, and Zn in seawater samples collected at sites GA-1 and EM-1 in two campaigns were below 0.33, 1.67, 0.47, 0.70, 2.86 ng mL(-1) respectively. For the first time, labile levels of Cd, Cu, Pb, Ni, and Zn in an area under the influence of oil production were determined. DGT measurements allowed the verification of the effects of temporal variation on levels of Zn and Ni. There were no effects of spatial variations on levels of Cd, Cu, Ni, Pb, and Zn at the four studied sites, suggesting no contamination of these metals at the northeastern Brazilian coastal area investigated in this work. Copyright © 2014. Published by Elsevier B.V.

Cation exchange removal of Cd from aqueous solution by NiO

International Nuclear Information System (INIS)

Mahmood, T.; Saddique, M.T.; Naeem, A.; Mustafa, S.; Dilara, B.; Raza, Z.A.

2011-01-01

Graphical abstract: Sorption of Cd on NiO particles is described by modified Langmuir adsorption isotherms. - Abstract: Detailed adsorption experiments of Cd from aqueous solution on NiO were conducted under batch process with different concentrations of Cd, time and temperature of the suspension. The solution pH is found to play a decisive role in the metal ions precipitation, surface dissolution and adsorption of metal ions onto the NiO. Preliminary adsorption experiments show that the selectivity of NiO towards different divalent metal ions follows the trend Pb > Zn > Co > Cd, which is related to their first hydrolysis equilibrium constant. The exchange between the proton from the NiO surface and the metal from solution is responsible for the adsorption. The cation/exchange mechanism essentially remains the same for Pb, Zn, Co and Cd ions. The sorption of Cd on NiO particles is described by the modified Langmuir adsorption isotherms. The isosteric heat of adsorption (ΔH) indicates the endothermic nature of the cation exchange process. Spectroscopic analyses provide evidence that Cd is chemisorbed onto the surface of NiO.

The Enrichment and Transfer of Heavy Metals for Two Ferns in Pb-Zn Tailing

Directory of Open Access Journals (Sweden)

Mai Jiajie

2017-01-01

Full Text Available The enrichment and transfer of 8 heavy metals of Equisetum ramosissimum and Pteris vittata growing naturally close to edge of the sewage pool in Bencun Pb-Zn Tailing, Eastern Guangdong were investigated. The results indicated that the pollution of Cd, Pb, Hg, Zn was very severe in this tailing, followed by Cu and Mn. The potential ecological risk of heavy metals was assessed to be very strong based on soil background values of Guangdong Province and at high risk according to criteria of the second grade State Soil Environmental Quality Standard, and Cd, Hg, Pb were the main factors leading to potential ecological risk. The content of 8 heavy metals in the two ferns did not reach critical content of hyperaccumulator, so neither of them was typical hyperaccumulator, but both had a certain tolerance to these heavy metal pollution. Underground parts of Pteris vittata had an enrichment coefficient above 1 and that of Equisetum ramosissimum had a value near 1, therefore the two ferns could be utilized as potential enrichment plants. The two ferns have strong adaptability to the tailing habitat and can be used as pioneers in ecological restoration of Pb-Zn tailings.

Thermopower of thermoelectric materials with resonant levels: PbTe:Tl versus PbTe:Na and Cu1 -xNix

Science.gov (United States)

Wiendlocha, Bartlomiej

2018-05-01

Electronic transport properties of thermoelectric materials containing resonant levels are discussed by analyzing the two best known examples: copper-nickel metallic alloy (Cu-Ni, constantan) and thallium-doped lead telluride (PbTe:Tl). As a contrasting example of a material with a nonresonant impurity, sodium-doped PbTe is considered. Theoretical calculations of the electronic structure, Bloch spectral functions, and energy-dependent electrical conductivity at T =0 K are done using the Korringa-Kohn-Rostoker method with the coherent potential approximation and the Kubo-Greenwood formalism. The effect of a resonance on the residual resistivity and electronic lifetimes in PbTe is analyzed. By using the full Fermi integrals, room-temperature thermopower is calculated, confirming its increase in PbTe:Tl versus PbTe:Na, due to the presence of the resonant level. In addition, our calculations support the self-compensation model, in which the experimentally observed reduction of carrier concentration in PbTe:Tl against the nominal one is explained by the presence of n -type Te vacancies.

Metals and arsenic in soils and corresponding vegetation at Central Elbe river floodplains (Germany)

Energy Technology Data Exchange (ETDEWEB)

Overesch, M. [Department for Geo- and Agroecology, Institute of Spatial Analysis and Planning in Areas of Intensive Agriculture, University of Vechta, P.O. Box 1553, D-49364 Vechta (Germany)]. E-mail: moveresch@ispa.uni-vechta.de; Rinklebe, J. [Department of Soil Science, UFZ Center for Environmental Research Leipzig-Halle, Theodor-Lieser-Strasse 4, D-06120 Halle (Germany)]. E-mail: joerg.rinklebe@ufz.de; Broll, G. [Department for Geo- and Agroecology, Institute of Spatial Analysis and Planning in Areas of Intensive Agriculture, University of Vechta, P.O. Box 1553, D-49364 Vechta (Germany)]. E-mail: gbroll@ispa.uni-vechta.de; Neue, H.-U. [Department of Soil Science, UFZ Center for Environmental Research Leipzig-Halle, Theodor-Lieser-Strasse 4, D-06120 Halle (Germany)]. E-mail: heinz-ulrich.neue@ufz.de

2007-02-15

Floodplain soils at the Elbe river are frequently polluted with metals and arsenic. High contents of these pollutants were detected down to subsoil layers. NH{sub 4}NO{sub 3}-extractable (phytoavailable) Cd, Ni, and Zn were elevated in horizons with high acidity. Among five common floodplain plant species, Artemisia vulgaris showed highest concentrations of Cd, Cu, and Hg, Alopecurus pratensis of As and Phalaris arundinacea of Ni, Pb, and Zn. Relationships were weak between metal concentrations in plants and phytoavailable stocks in soil. As and Hg uptake seems to be enhanced on long submerged soils. Enrichments of Cd and Hg are linked to a special plant community composition. Grassland herbage sampled in July/August revealed higher concentrations of As (+122%), Hg (+124%), and Pb (+3723%) than in May. To limit harmful transfers into the food chain, low-lying terraces and flood channels revealing highest contaminations or phytoavailabilities should be excluded from mowing and grazing. - Soils in the Elbe river floodplains are highly polluted with metals and arsenic and a critical enrichment in the grassland herbage seems to be most likely in flood channels or within special plant species.

Associations between standardized school performance tests and mixtures of Pb, Zn, Cd, Ni, Mn, Cu, Cr, Co, and V in community soils of New Orleans

International Nuclear Information System (INIS)

Zahran, Sammy; Mielke, Howard W.; Weiler, Stephan; Hempel, Lynn; Berry, Kenneth J.; Gonzales, Christopher R.

2012-01-01

In New Orleans a strong inverse association was previously identified between community soil lead and 4th grade school performance. This study extends the association to zinc, cadmium, nickel, manganese, copper, chromium, cobalt, and vanadium in community soil and their comparative effects on 4th grade school performance. Adjusting for poverty, food security, racial composition, and teacher-student ratios, regression results show that soil metals variously reduce and compress student scores. Soil metals account for 22%–24% while food insecurity accounts for 29%–37% of variation in school performance. The impact on grade point averages were Ni > Co > Mn > Cu ∼Cr ∼ Cd > Zn > Pb, but metals are mixtures in soils. The quantities of soil metal mixtures vary widely across the city with the largest totals in the inner city and smallest totals in the outer city. School grade point averages are lowest where the soil metal mixtures and food insecurity are highest. - Highlights: ► Mixtures of metals vary; largest totals in the inner city and lowest in the outer city. ► An inverse association between soil Pb and 4th grade school performance is known. ► Assuming the same exposure pathway, multiple metals are compared to performance. ► Soil metals account for 22%–24% of variation in school test performance. ► Soil metal plus food insecurity accounts for 54% of explained variance. - Controlling for potential confounding variables, the accumulation of metals (Pb, Zn, Cd, Ni, Mn, Cu, Cr, and Co) in neighborhood soils is significantly negatively associated with 4th grade school performance on standardized tests in New Orleans.

Metales pesados en tejido muscular del bagre Ariopsis felis en el sur del golfo de México (2001-2004 Heavy metals in muscular tissue of the catfish, Ariopsis felis, in the southern Gulfof México (2001-2004

Directory of Open Access Journals (Sweden)

Felipe Vázquez

2008-01-01

Full Text Available Se analizó el contenido de metales pesados en tejido muscular del bagre, Ariopsis felis en el sur del golfo de México durante el período 2001-2004. La investigación fue efectuada buscando establecer un marco de referencia ambiental para este organismo. La concentración metálica siguió el orden: Hg We analyzed the heavy metal content in the muscular tissue of the catfish, Ariopsis felis, in the southern Gulf of México between 2001 and 2004. The research was done in order to establish an environmental frame of reference for this organism. The metal concentration was as follows: Hg < Co < Pb < Ni < V < Cr. Cobalt and vanadium contents were found to decrease and those of nickel, mercury, and chromium to ulerease; however, neither of these trends was observed for the lead content. One-way analyses of variance con-firm significant temporal variation only for cobalt, mercury, lead, and vanadium. Significant linear correlation coefficients (p ≤ 0.05 were found for Co-V, Cr-Ni, Cr-Pb, Co-Hg, Ni-V, and V-Pb. The first three associa-tions showed positive correlations, whereas the remaining ones had negative correlations. A factor analysis grouped the studied metals depending on their origins. The metal levels found in the muscular tissue of A. felis from the southern Gulf of México were lower than those set by national and international regulations.

A thermodynamic stability of bulk and epitaxial CdHgTe, ZnHgTe and MnHgTe solid solutions

International Nuclear Information System (INIS)

Dejbuk, V.G.; Dremlyuzhenko, S.G.; Ostapov, S.Eh.

2005-01-01

A thermodynamics of Cd 1-x Hg x Te, Zn x Hg 1-x Te and Mg x Hg 1-x Te alloys has been investigated for a delta-lattice parameter model. The phase diagrams obtained show the stability of Cd 1-x Hg x Te, Zn x Hg 1-x Te in the whole range of compositions, alongside with a miscibility gap for Mn x Hg 1-x Te being of 0.35 x Hg 1-x Te/CdTe and Mn x Hg 1-x Te/Cd 0.96 Zn 0.04 Te epitaxial films result in lowering critical temperatures and narrowing the miscibility gap [ru

Sources of heavy metal pollution in agricultural soils of a rapidly industrializing area in the Yangtze Delta of China.

Science.gov (United States)

Xu, Xianghua; Zhao, Yongcun; Zhao, Xiaoyan; Wang, Yudong; Deng, Wenjing

2014-10-01

The rapid industrialization and urbanization in developing countries have increased pollution by heavy metals, which is a concern for human health and the environment. In this study, 230 surface soil samples (0-20cm) were collected from agricultural areas of Jiaxing, a rapidly industrializing area in the Yangtze Delta of China. Sequential Gaussian simulation (SGS) and multivariate factorial kriging analysis (FKA) were used to identify and explore the sources of heavy metal pollution for eight metals (Cu, Zn, Pb, Cr, Ni, Cd, Hg and As). Localized hot-spots of pollution were identified for Cu, Zn, Pb, Cr, Ni and Cd with area percentages of 0.48 percent, 0.58 percent, 2.84 percent, 2.41 percent, 0.74 percent, and 0.68 percent, respectively. The areas with Hg pollution covered approximately 38 percent whereas no potential pollution risk was found for As. The soil parent material and point sources of pollution had significant influences on Cr, Ni, Cu, Zn and Cd levels, except for the influence of agricultural management practices also accounted for micro-scale variations (nugget effect) for Cu and Zn pollution. Short-range (4km) diffusion processes had a significant influence on Cu levels, although they did not appear to be the dominant sources of Zn and Cd variation. The short-range diffusion pollution arising from current and historic industrial emissions and urbanization, and long-range (33km) variations in soil parent materials and/or diffusion jointly determined the current concentrations of soil Pb. The sources of Hg pollution risk may be attributed to the atmosphere deposition of industrial emission and historical use of Hg-containing pesticides. Copyright © 2014 Elsevier Inc. All rights reserved.

A feasibility study on SnO2/NiFe2O4 nanocomposites as anodes for Li ion batteries

International Nuclear Information System (INIS)

Balaji, S.; Vasuki, R.; Mutharasu, D.

2013-01-01

Highlights: ► The morphological analysis performed has shown the existence of nanocomposite. ► Sp. capacity after 50 cycles of pure NiFe 2 O 4 , 5 and 10 wt.% SnO 2 are 450, 750 and 780 mA h/g. ► The results are higher than the theoretical capacity of graphite (374 mA h/g). ► The capacity retention is also found to increase with SnO 2 addition in the NiFe 2 O 4 . ► Charge and discharge capacities of LiMn 2 O 4 vs. 10 wt.% SnO 2 /NiFe 2 O 4 are 232 and 138 mA h/g. -- Abstract: The SnO 2 /NiFe 2 O 4 nanocomposite samples with varying concentration of SnO 2 such as 5 wt.% and 10 wt.% were synthesized via urea assisted combustion synthesis. The kinetics of the combustion reactions were studied using thermo gravimetry analysis and from which the compound formation temperature of all the samples were observed to be below 400 °C. From the morphological analysis the grain size of NiFe 2 O 4 , 5 wt.% SnO 2 /NiFe 2 O 4 and 10 wt.% SnO 2 /NiFe 2 O 4 samples were observed to be around 1.7, 2.3 and 3.5 μm. The chrono potentiometry analyses of the samples were performed against lithium metal electrode. The capacity retention was found to be higher for composite with 10 wt.% SnO 2 . The discharge capacity of 10 wt.% SnO 2 sample with respect to Li metal and LiMn 2 O 4 electrode was observed to be around 980 mA h/g and 138 mA h/g respectively

Zuotai and HgS differ from HgCl2 and methyl mercury in Hg accumulation and toxicity in weanling and aged rats.

Science.gov (United States)

Zhang, Bin-Bin; Li, Wen-Kai; Hou, Wei-Yu; Luo, Ya; Shi, Jing-Zhen; Li, Cen; Wei, Li-Xin; Liu, Jie

2017-09-15

Mercury sulfides are used in Ayurvedic medicines, Tibetan medicines, and Chinese medicines for thousands of years and are still used today. Cinnabar (α-HgS) and metacinnabar (β-HgS) are different from mercury chloride (HgCl 2 ) and methylmercury (MeHg) in their disposition and toxicity. Whether such scenario applies to weanling and aged animals is not known. To address this question, weanling (21d) and aged (450d) rats were orally given Zuotai (54% β-HgS, 30mg/kg), HgS (α-HgS, 30mg/kg), HgCl 2 (34.6mg/kg), or MeHg (MeHgCl, 3.2mg/kg) for 7days. Accumulation of Hg in kidney and liver, and the toxicity-sensitive gene expressions were examined. Animal body weight gain was decreased by HgCl 2 and to a lesser extent by MeHg, but unaltered after Zuotai and HgS. HgCl 2 and MeHg produced dramatic tissue Hg accumulation, increased kidney (kim-1 and Ngal) and liver (Ho-1) injury-sensitive gene expressions, but such changes are absent or mild after Zuotai and HgS. Aged rats were more susceptible than weanling rats to Hg toxicity. To examine roles of transporters in Hg accumulation, transporter gene expressions were examined. The expression of renal uptake transporters Oat1, Oct2, and Oatp4c1 and hepatic Oatp2 was decreased, while the expression of renal efflux transporter Mrp2, Mrp4 and Mdr1b was increased following HgCl 2 and MeHg, but unaffected by Zuotai and HgS. Thus, Zuotai and HgS differ from HgCl 2 and MeHg in producing tissue Hg accumulation and toxicity, and aged rats are more susceptible than weanling rats. Transporter expression could be adaptive means to reduce tissue Hg burden. Copyright © 2017 Elsevier Inc. All rights reserved.

Assessment of metals pollution on agricultural soil surrounding a lead-zinc mining area in the Karst region of Guangxi, China.

Science.gov (United States)

Zhang, Chaolan; Li, Zhongyi; Yang, Weiwei; Pan, Liping; Gu, Minghua; Lee, DoKyoung

2013-06-01

Soil samples were collected on farmland in a lead-zinc mining area in the Karst region of Guangxi, China. The contamination of the soil by eight metals (Cd, Hg, As, Cu, Pb, Cr, Zn, Ni) was determined. Among all these metals, Cd is the most serious pollutant in this area. Zn, Hg as well asPb can also be measured at high levels, which may affect the crop production. All other metals contributed marginally to the overall soil contamination. Besides the evaluation of single metals, the Nemerow synthetic index indicated that the soil is not suitable for agricultural use.

Sediment quality assessment in a coastal lagoon (Ravenna, NE Italy) based on SEM-AVS and sequential extraction procedure.

Science.gov (United States)

Pignotti, Emanuela; Guerra, Roberta; Covelli, Stefano; Fabbri, Elena; Dinelli, Enrico

2018-09-01

Sediments from the Pialassa Piomboni coastal lagoon (NE Italy) were studied to assess the degree of contamination and ecological risk related to trace metals by combining a geochemical characterization of bulk sediments with the assessment of the bioavailable forms of trace metals. With this purpose, sediment contamination (Cd, Cu, Hg, Ni, Pb, and Zn) was assessed by Enrichment Factors (EFs), and potential bioavailability by the Simultaneously Extracted Metals and Acid Volatile Sulfides (SEM-AVS) approach (Cd, Cu, Ni, Pb, and Zn), and by Sequential Extraction Procedure (Co, Cr, Cu, Ni, Pb, and Zn). On average, Cr and Ni exhibited no contamination (EF ≤1.5), and a predominance in the residual fraction of the sediment, indicating natural origin for these metals. Cu, Pb and Zn displayed a local contamination, which resulted in a higher proportion of Cu bound to the reducible and oxidizable fractions (~30% and ~40% as median, respectively), and Pb mostly associated with the reducible phase (~60% as median). Hence, Cu and Pb could be mobilized when environmental conditions become reducing or oxidizing. Zn resulted mainly partitioned into the reducible and residual fractions (~50% as median, in both fractions). The Risk Assessment Code (RAC) indicated that approximately 30% of samples had >10% of total Zn weakly bound to the sediment, suggesting a medium risk of exposure for aquatic organisms. RAC results were consistent with the ∑SEM-AVS findings, pointing to possible adverse effects for aquatic biota in ~30% of samples, with Zn mostly accounting for the total metal bioavailability. Hg showed a moderate to very severe enrichment, indicating that a substantial amount of this metal derives from anthropogenic sources and may pose adverse effects on the aquatic biota of the Pialassa Piomboni lagoon. Copyright © 2018 Elsevier B.V. All rights reserved.

A portable optical emission spectroscopy-cavity ringdown spectroscopy dual-mode plasma spectrometer for measurements of environmentally important trace heavy metals: Initial test with elemental Hg

Science.gov (United States)

Sahay, Peeyush; Scherrer, Susan T.; Wang, Chuji

2012-09-01

A portable optical emission spectroscopy-cavity ringdown spectroscopy (OES-CRDS) dual-mode plasma spectrometer is described. A compact, low-power, atmospheric argon microwave plasma torch (MPT) is utilized as the emission source when the spectrometer is operating in the OES mode. The same MPT serves as the atomization source for ringdown measurements in the CRDS mode. Initial demonstration of the instrument is carried out by observing OES of multiple elements including mercury (Hg) in the OES mode and by measuring absolute concentrations of Hg in the metastable state 6s6p 3P0 in the CRDS mode, in which a palm-size diode laser operating at a single wavelength 405 nm is incorporated in the spectrometer as the light source. In the OES mode, the detection limit for Hg is determined to be 44 parts per 109 (ppb). A strong radiation trapping effect on emission measurements of Hg at 254 nm is observed when the Hg solution concentration is higher than 50 parts per 106 (ppm). The radiation trapping effect suggests that two different transition lines of Hg at 253.65 nm and 365.01 nm be selected for emission measurements in lower (50 ppm), respectively. In the CRDS mode, the detection limit of Hg in the metastable state 6s6p 3P0 is achieved to be 2.24 parts per 1012 (ppt) when the plasma is operating at 150 W with sample gas flow rate of 480 mL min-1; the detection limit corresponds to 50 ppm in Hg sample solution. Advantage of this novel spectrometer has two-fold, it has a large measurement dynamic range, from a few ppt to hundreds ppm and the CRDS mode can serve as calibration for the OES mode as well as high sensitivity measurements. Measurements of seven other elements, As, Cd, Mn, Ni, P, Pb, and Sr, using the OES mode are also carried out with detection limits of 1100, 33, 30, 144, 576, 94, and 2 ppb, respectively. Matrix effect in the presence of other elements on Hg measurements has been found to increase the detection limit to 131 ppb. These elements in lower

Goods in the Anthroposphere as a Metal Emission Source A Case Study of Stockholm, Sweden

International Nuclear Information System (INIS)

Soerme, L.; Bergbaeck, B.; Lohm, U.

2001-01-01

The aim of this study was to quantify the diffuse emissions during use of metal containing goods in the capital of Sweden,Stockholm. The following metals were studied: Cadmium (Cd), Chromium (Cr), Copper (Cu), Lead (Pb), Mercury (Hg), Nickel (Ni) and Zinc (Zn).A major part of the metals are found in a protected environment where degrading processes like corrosion are most limited. However, during the lifetime of some goods the metal release to the environment is significant. The quantitatively most dominant emissions were found for Cu and Zn. The tap water system and roofs/fronts (Cu) represent goods with large exposed areas but with relatively small release rates per unit. In contrast, brake linings, aerial lines and electrical grounding (Cu) and tyres, brake linings and chemicals (Zn) are all goods with high release rates but mostly limited exposed stocks.High yearly emissions are also found for Pb, ammunition and sinkers dominate the calculated emissions totally. For Cr and Ni, stainless steel represent the major part of the stocks, but corrosion was estimated to give only a minor contribution to the emissions. Potential emission sources, i.e. stabilisers,pigments and plated goods dominate the exposed Cd stock. These emissions were not quantified due to lack of data. Hg is currently phased out, but one major source of emission, i.e. the use of amalgam, will be continuously significant for several decades. The importance of the traffic sector is obvious. The emissions from brake linings (Cu, Zn and Pb), tyres (Zn, Pb, Cr and Ni)and asphalt wear (Cu, Zn, Cr, Ni and Pb) are all of large importance for the total emission from respectively metal

Heavy metals in soils and crops in Southeast Asia. 1. Peninsular Malaysia.

Science.gov (United States)

Zarcinas, Bernhard A; Ishak, Che Fauziah; McLaughlin, Mike J; Cozens, Gill

2004-12-01

In a reconnaisance soil geochemical and plant survey undertaken to study the heavy metal uptake by major food crops in Malaysia, 241 soils were analysed for cation exchange capacity (CEC), organic carbon (C), pH, electrical conductivity (EC) and available phosphorus (P) using appropriate procedures. These soils were also analysed for arsenic (As), cadmium (Cd), cobalt (Co), chromium (Cr), copper (Cu), mercury (Hg), nickel (Ni), lead (Pb) and zinc (Zn) using aqua regia digestion, together with 180 plant samples using nitric acid digestion. Regression analysis between the edible plant part and aqua regia soluble soil As, Cd, Cr, Cu, Hg, Ni, Pb and Zn concentrations sampled throughout Peninsular Malaysia, indicated a positive relationship for Pb in all the plants sampled in the survey (R2 = 0.195, p contamination of soils by these elements through agricultural activities is not strong. Chromium was correlated with soil pH and EC, Na, S, and Ca while Hg was not correlated with any of these components, suggesting diffuse pollution by aerial deposition. However As, Cd, Cu were strongly associated with organic matter and available and aqua regia soluble soil P, which we attribute to inputs in agricultural fertilisers and soil organic amendments (e.g. manures, composts).

Multivariate statistical and GIS-based approach to identify source of anthropogenic impacts on metallic elements in sediments from the mid Guangdong coasts, China

International Nuclear Information System (INIS)

Gu Yangguang; Wang, Zhao-Hui; Lu Songhui; Jiang Shijun; Mu Dehai; Shu Yonghong

2012-01-01

Growing concerns surround the mid Guangdong coasts, one of China’s fastest and developing economical regions. To study the environmental impacts of economic and industrial development, we measured ten metallic elements (Hg, Pb, Cu, Zn, Fe, Al, Ni, Sr, Li, and Co) in surface sediments from nineteen stations in three bays. All these metals showed concentrations substantially higher than their background values, suggesting possible anthropogenic pollution. Highest metal levels were close to the nuclear power plants likely as a result of nuclear waste discharges. Results revealed that Hg, Pb, and Sr largely originated from human activities, while Cu, Ni, Co, Al, and Fe mainly from natural rock weathering. Two types of anthropogenic sources were identified through a principal component analysis, one from shipping industry, port transport service and nuclear power plants, and the other from municipal sewage and coal power plant. - Highlights: ► Ten metallic elements in surface sediments from mid Guangdong coasts were measured. ► High metal levels occurred close to the nuclear power plants. ► Hg, Pb and Sr mainly originated from human activities. ► Two types of anthropogenic metallic sources were identified in this region. - Hot spots of metallic elements were close to the nuclear power plants. Industrial and municipal discharges were the main anthropogenic metallic source.

199Hg Moessbauer measurements on mercury, alloys and Hg-fluorides

International Nuclear Information System (INIS)

Wurtinger, W.; Kankeleit, E.

1979-01-01

The Moessbauer effect on the 158 keV 5/2 - -1/2 - transition in 199 Hg, of the order of 10 ppm, has been studied using the current integration technique. The isomer shift between the Hg(I)- and Hg(II)-fluorides as well as the quadrupole splitting in Hg 2 Pt and Hg 2 F 2 are interpreted in terms of relativistic Hartree-Fock-Slater and Molecular Orbital calculations. The following nuclear parameters could be derived: Δ[r 2 ] = (3.2+-1.1) 10 -3 fm 2 and Q(5/2 - ) = (-0.8+-0.4)b. Evidence for an oblate triaxially deformed 199 Hg nucleus is derived from particle plus rotor calculations. (orig.)

Determination of Cr, Cu, Fe, Ni, Pb and Zn by ICP-OES in mushroom samples from Sakarya, Turkey

Directory of Open Access Journals (Sweden)

Esra Altıntığ

2017-06-01

Full Text Available Russula cyanoxantha, Russula delica, Lactarius salmonicolor, Lactarius deliciosus, Pleurotus eryngii, Pleurotus ostreatus, Agaricus bisporus, Suillus luteus, Pleurotus spp and Boletus edulis were collected from Sakarya-Turkey respectively. Also canned food in the form of the Pleurotus eryngii, Pleurotus ostreatus, and Lactarius salmonicolor mushrooms were used for the examination. Trace metal concentrations found in these mushrooms were determined inductively using coupled plasma optic emission spectrometry microwave processes. The results were obtained for (Cr 0.3-26.65, (Cu 17.38-132.75, (Fe 26.3-225.40, (Ni 2.57-39.28, (Pb 11.52-185.20, and (Zn 22.86-126.84 mg/kg. The accuracy of the method was checked by the standard reference material; tea leaves (INCY-TL-1 and tomato leaves (1573a.

Depth profile distribution of Cr, Cu, Co, Ni and Pb in the sediment cores of Mumbai Harbour Bay

International Nuclear Information System (INIS)

Madhuparna, D.; Hemalatha, P.; Raj, Sanu S.; Jha, S.K.; Tripathi, R.M.

2014-01-01

Estuarine and coastal sediments act as ultimate sink for trace metals that are discharged into the aquatic environment. Sources of environmental contaminants to the coastal system are numerous and may enter the estuarine environment via a number of pathways Mumbai Harbour Bay on the western coast of India, receives low level nuclear wastes and industrial and domestic sewage waste from the surrounding dwellings. Also, the bay is extensively exploited for various other local activities. The present study was carried out in the bay sediment cores to investigate the depth profile distribution of trace element concentration. Biologically significant toxic elements such as Cr, Cu, Co, Ni and Pb were estimated in the sediment cores to find out pattern of distribution in the sediment bed to follow the accumulation of elements with respect to depth

An integrated approach to assess heavy metal source apportionment in peri-urban agricultural soils.

Science.gov (United States)

Huang, Ying; Li, Tingqiang; Wu, Chengxian; He, Zhenli; Japenga, Jan; Deng, Meihua; Yang, Xiaoe

2015-12-15

Three techniques (Isotope Ratio Analysis, GIS mapping, and Multivariate Statistical Analysis) were integrated to assess heavy metal pollution and source apportionment in peri-urban agricultural soils. The soils in the study area were moderately polluted with cadmium (Cd) and mercury (Hg), lightly polluted with lead (Pb), and chromium (Cr). GIS Mapping suggested Cd pollution originates from point sources, whereas Hg, Pb, Cr could be traced back to both point and non-point sources. Principal component analysis (PCA) indicated aluminum (Al), manganese (Mn), nickel (Ni) were mainly inherited from natural sources, while Hg, Pb, and Cd were associated with two different kinds of anthropogenic sources. Cluster analysis (CA) further identified fertilizers, waste water, industrial solid wastes, road dust, and atmospheric deposition as potential sources. Based on isotope ratio analysis (IRA) organic fertilizers and road dusts accounted for 74-100% and 0-24% of the total Hg input, while road dusts and solid wastes contributed for 0-80% and 19-100% of the Pb input. This study provides a reliable approach for heavy metal source apportionment in this particular peri-urban area, with a clear potential for future application in other regions. Copyright © 2015 Elsevier B.V. All rights reserved.

RDDS lifetime measurements of low-lying superdeformed states in {sup 194}Hg

Energy Technology Data Exchange (ETDEWEB)

Kuehn, R.; Dewald, A.; Kruecken, R. [Universitaet Koeln (Germany)] [and others

1996-12-31

The lifetimes of three low-lying states in the superdeformed (SD) yrast band of {sup 194}Hg were measured by the recoil-distance Doppler-shift method. The deduced transition quadrupole moments, Q{sub t}, equal those extracted from a DSAM measurement for the high-lying states of the band corroborate the assumption that the decay out of SD bands does not strongly affect the structure of the corresponding states. By a simple mixing-model the decay can be described assuming a very small admixture of normal-deformed (ND) states to the decaying SD states. The deduced ND mixing amplitudes for the yrast SD bands in {sup 192,194}Hg and {sup 194}Pb are presented along with average transition quadrupole moments for the lower parts of the excited SD bands.

Concentrations of 17 elements, including mercury, and their relationship to fitness measures in arctic shorebirds and their eggs.

Science.gov (United States)

Hargreaves, Anna L; Whiteside, Douglas P; Gilchrist, Grant

2010-07-15

Exposure to contaminants is one hypothesis proposed to explain the global decline in shorebirds, and this is of particular concern in the arctic. However, little information exists on contaminant levels in arctic-breeding shorebirds, especially in Canada. We studied potential contaminants in three biparental shorebird species nesting in Nunavut, Canada: ruddy turnstones (Arenaria interpres), black-bellied plovers (Pluvialis squatarola) and semipalmated plovers (Charadrius semipalmatus). Blood, feathers and eggs were analyzed for As, Be, Cd, Co, Cr, Cu, Fe, Hg, Mn, Mo, Ni, Pb, Sb, Se, Tl, V, and Zn. We assessed whether element concentrations a) differed among species and sexes, b) were correlated among pairs and their eggs, and c) were related to fitness endpoints, namely body condition, blood-parasite load, nest survival days, and hatching success. Non-essential elements were found at lower concentrations than essential elements, with the exception of Hg. Maximum Hg levels in blood approached those associated with toxicological effects in other bird species, but other elements were well below known toxicological thresholds. Reproductive success was negatively correlated with paternal Hg and maternal Pb, although these effects were generally weak and varied among tissues. Element levels were positively correlated within pairs for blood-Hg (turnstones) and feather-Ni and Cr (semipalmated plovers); concentrations in eggs and maternal blood were never correlated. Concentrations of many elements differed among species, but there was no evidence that any species had higher overall exposure to non-essential metals. In conclusion, whereas we found little evidence that exposure to the majority of these elements is leading to declines of the species studied here, Hg levels were of potential concern and both Hg and Pb warrant further monitoring. Copyright 2010 Elsevier B.V. All rights reserved.

In Situ Characterization of Ni and Ni/Fe Thin Film Electrodes for Oxygen Evolution in Alkaline Media by a Raman-Coupled Scanning Electrochemical Microscope Setup.

Science.gov (United States)

Steimecke, Matthias; Seiffarth, Gerda; Bron, Michael

2017-10-17

We present a spectroelectrochemical setup, in which Raman microscopy is combined with scanning electrochemical microscopy (SECM) in order to provide both spectroscopic and electrochemical information on the very same location of an electrode at the same time. The setup is applied to a subject of high academic and practical interest, namely, the oxygen evolution reaction at Ni and Ni/Fe electrodes. It comprises a transparent substrate electrode, onto which Ni and Ni/Fe thin films are deposited. An ultramicroelectrode (UME) is placed closely above the substrate to obtain electrochemical information, while a Raman microscope probes the same sample spot from below. To obtain information on oxygen evolution activity and structural changes, increasingly positive potentials from 0.1 up to 0.7 V vs Hg|HgO|1 M KOH were applied to the Ni/Fe-electrodes in 0.1 M KOH solution. Evolved oxygen is detected by reduction at a Pt UME, allowing for the determination of onset potentials, while the substrate current, which is recorded in parallel, is due to both overlapping oxygen evolution and the oxidation of Ni(OH) 2 to NiOOH. An optimum of 15% Fe in Ni/Fe films with respect to oxygen evolution activity was determined. At the same time, the potential-dependent formation of γ-NiOOH characterized by the Raman double band at 475 and 557 cm -1 allows for the conclusion that a certain amount of disorder introduced by Fe atoms is necessary to obtain high oxygen evolution reaction (OER) activity.

Pb-Zn-Cd-Hg multi isotopic characterization of the Loire River Basin, France

Science.gov (United States)

Millot, R.; Widory, D.; Innocent, C.; Guerrot, C.; Bourrain, X.; Johnson, T. M.

2012-12-01

The contribution of human activities such as industries, agriculture and domestic inputs, becomes more and more significant in the chemical composition (major ions and pollutants such as metals) of the dissolved load of rivers. Furthermore, this influence can also be evidenced in the suspended solid matter known to play an important role in the transport of heavy metals through river systems. Human factors act as a supplementary key process. Therefore the mass-balance for the budget of catchments and river basins include anthropogenic disturbances. The Loire River in central France is approximately 1010 km long and drains an area of 117,800 km2. Initially, the Loire upstream flows in a south to north direction originating in the Massif Central, and continues up to the city of Orléans, 650 km from the source. In the upper basin, the bedrock is old plutonic rock overlain by much younger volcanic rocks. The Loire River then follows a general east to west direction to the Atlantic Ocean. The intermediate basin includes three major tributaries flowing into the Loire River from the left bank: the Cher, the Indre and the Vienne rivers; the main stream flows westward and its valley stretches toward the Atlantic Ocean. Here, the Loire River drains the sedimentary series of the Paris Basin, mainly carbonate deposits. The lower Loire basin drains pre-Mesozoic basement of the Armorican Massif and its overlying Mesozoic to Cenozoic sedimentary deposits. The Loire River is one of the main European riverine inputs to the Atlantic ocean. Here we are reporting concentration and isotope data for heavy metals Zn-Cd-Pb-Hg in river waters and suspended sediments from the Loire River Basin. In addition, we also report concentration and isotope data for these metals for the different industrial sources within the Loire Basin, as well as data for biota samples such as mussels and oysters from the Bay of Biscay and North Brittany. These organisms are known to be natural accumulators of

Impact of chirano gold mines operations on levels of As, Pb, Hg and Cd in the suraw river and the possible health implications on downstream communities

International Nuclear Information System (INIS)

Oppong, Kyekyeku

2011-07-01

Suraw River water quality awareness and preference survey conducted in five immediate downstream communities indicated that the residents were very much aware of the changes that have occurred since the commencement of active mining by CGML last quarter in 2004. Notwithstanding the residents overwhelming preference for the borehole water for their basic water needs including drinking, some people still rely on the River water when they go to their farms. Suraw River which principally drains the surface waters of Chirano Gold Mines operational area was investigated to assess the levels of As, Cd, Pb and Hg in the River water, bottom sediments and community borehole water using Atomic Absorption Spectrophotometer and Inductively Coupled Plasma - Optical Emission Spectroscopy (ICP – OES) for the water and sediments respectively. The results of the study generally showed low to below laboratory detection levels for the four heavy metals under investigation. The occurrence of Arsenic in more than half of the sampling sites in both the Suraw River and the community boreholes and particularly its detection at S1 in the surface water samples are most probably as a result of natural background levels. Except Cadmium which exceeded the Lowest Effect Level (LEL) in the sediment samples, the concentration of As, Pb and Hg were below the LEL of toxicity. The concentration of Cd also exceeded the Threshold Effect and the Probable Effect Levels but lower than the Severe Effect Level of sediment toxicity at five of the six sampling sites. The study has shown that the concentration of the four heavy metals investigated in both the Suraw River and the community borehole water were lower than expected compared with WHO/GWCL Drinking Water Standards and were within acceptable limits for potable water and therefore do not pose any immediate health risk to residents and settler farmers who still depend on the River water for their basic water needs. Apart from the concentration of Cd

Diffusion of Cs, Ni, Pb, Se through MX80 bentonite and Bure argilite

International Nuclear Information System (INIS)

Kedziorek, M.A.M.; Bourg, A.C.M.

2010-01-01

Document available in extended abstract form only. In order to isolate nuclear waste in repositories from the biosphere two characteristics are required from the confining environment: adsorption as high as possible and permeability as low as possible. In France, bentonite (MX80) and argillite from the Bure underground laboratories are the candidates for the near- and far-field barriers, respectively. To investigate interactive diffusive transport, we performed a series of diffusion experiments in experimental cells. 'Through' diffusion and 'in' diffusion protocols were followed and performed for a cocktail of Cs, Ni, Pb and Se, this under a variety of conditions susceptible of affecting adsorption and diffusive transport, i.e. solid density, water pH and ionic strength. For the argillite experiments the solution pH and solid density are controlled by the solid. The MX80 bentonite was pretreated according to the proposed experimental solution pH and ionic strength. The reservoirs (downstream for the 'through' diffusion experiments and upstream for the 'in' diffusion experiments were sampled at regular intervals and analyzed for the elements of interests. At the end of the experiments the solids were sliced and the elemental content analyzed. A series of results will be presented and preliminary interpretation proposed

Assessment of soil contamination by potentially toxic trace elements (PTSD) (As, Cd, Cu, Hg, Pb, Zn) in a lower plain of the Hron River according to Law no. 219/2008 Coll., by geo-accumulation index, anthropogenic factor and Tomlinson index; Zhodnotenie kontaminacie pod potencialne toxickymi stopovymi prvkami (PTSP) (As, Cd, Cu, Hg, Pb, Zn) v dolnej casti nivy Hrona podla zakona c. 219/2008 Z.z., indexu geoakumulacie, antropogenneho faktora a Tomlinsonovho indexu

Energy Technology Data Exchange (ETDEWEB)

Hlodak, M [Univerzita Komenskeho v Bratislave, Prirodovedecka fakulta, Ustav laboratorneho vyskumu geomaterialov, 84215 Bratislava (Slovakia)

2012-04-25

Soil contamination by different PTSD may have different geogenic and anthropogenic origin and occurs in all countries of the world. The aim of this paper is to evaluate the soils contamination of a lower plain of the Hron River. This paper used the results of the thesis Soil contamination of the Hron River floodplain by trace elements (As, Cd, Cu, Hg, Pb, Zn) [1]. Soil contamination was evaluated by: Act. 219/2008 Coll. on the protection and use of agricultural land, by anthropogenic factor (AF), geo-accumulation index (IgeoE) and Tomlinson index - the index of the pollution load (PLI). (author)

Heavy metals contamination and human health risk assessment around Obuasi gold mine in Ghana.

Science.gov (United States)

Bempah, Crentsil Kofi; Ewusi, Anthony

2016-05-01

Gold mining has increased the prevalence and occurrence of heavy metals contamination at the Earth's surface and is causing major concern due to the potential risk involved. This study investigated the impact of gold mine on heavy metals (As, Cd, Cr, Cu, Pb, Hg, Ni, Fe, Mn, and Zn) pollution and evaluated the potential health risks to local residents via consumption of polluted groundwater, agricultural soils, and vegetable crops grown at three community farms surrounding the mine at Obuasi municipality of Ghana. The results showed levels of As, Cd, Cr, Hg, Fe, and Mn higher than the allowable drinking water standards. The vegetable samples analyzed showed high accumulation of As and Ni above the normal value. Bioaccumulation factors of heavy metals were significantly higher for vegetables grown in the Sanso soils. Estimated average daily intake and hazard quotient for As in drinking water as well as As, Pb, and Hg in vegetable samples exceeded permissible limit. Unacceptable non-cancer health risk levels were found in vegetable samples analyzed for As, Pb, and Hg. An unacceptable cancer risk was found via drinking of groundwater, in consumption of vegetables, and in soil. The hazard index for vegetables was higher than 1, indicating very high health risk to heavy metals contamination through consumption of vegetables grown around the sampling sites. The results recommend the need for regular monitoring of groundwater and food crops to protect consumers' health.

[Heavy metals in environmental media around drinking water conservation area of Shanghai].

Science.gov (United States)

Shi, Gui-Tao; Chen, Zhen-Lou; Zhang, Cui; Bi, Chun-Juan; Cheng, Chen; Teng, Ji-Yan; Shen, Jun; Wang, Dong-Qi; Xu, Shi-Yuan

2008-07-01

The levels of heavy metals in Shanghai drinking water conservation area were determined, and the spatial distributions and main sources of heavy metals were investigated. Moreover, the ecological risk assessment of heavy metals was conducted. Some conclusions can be drawn as follows: (1) The average concentrations of Cd, Hg, Pb, Cu, Zn, Ni, Cr and As in road dust were 0.80, 0.23, 148.45, 127.52, 380.57, 63.17, 250.38 and 10.37 mg x kg(-1) respectively. In terms of the pollution level, the values of soils were relatively lower, with the mean contents of 0.16 (Cd), 0.33 (Hg), 30.14 (Pb), 30.66 (Cu), 103.79 (Zn), 24.04 (Ni), 65.75 (Cr) and 6.31 mg x kg(-1) (As) severally; meanwhile the average levels of heavy metals in vegetables were 0.010 (Cd), 0.016 (Hg), 0.36 (Pb), 12.80 (Cu), 61.69 (Zn), 2.04 (Ni), 2.41 (Cr) and 0.039 mg x kg(-1) (As) respectively. (2) Semivariogram and multivariate analysis indicated that heavy metals pollution of soils was induced by anthropogenic activities mostly, and the pollutants produced by traffic were the major source of heavy metals in road dust. (3) The order for heavy metal enrichment coefficients of vegetables was as following: Zn (0.589) > Cu (0.412) > 0.102 (Ni) > Cd (0.059) > Cr (0.061) > Hg (0.056) > Pb (0.012) > As (0.007), and the results indicated that Cd and Zn in vegetables were mainly from the soils, and the other metals were probably from the pollutants in the atmosphere. (4) Sediments in drinking water conservation area were probably derived from soils around; however, there was no significant relationship between heavy metals contents of them. (5) The results of ecological risk assessment of heavy metals showed that heavy metals in soils were in no-warning to warning situation, and warning to light-warning situation for road dust and vegetables. The fuzzy synthesis judgment for all the environmental media around drinking water conservation area was warning to light-warning.

Low Fatigue in Epitaxial Pb(Zr0.2Ti0.8)O3 on Si Substrates with LaNiO3 Electrodes by RF Sputtering

Science.gov (United States)

Wang, Chun; Kryder, Mark H.

2009-09-01

Epitaxial PZT (001) thin films with a LaNiO3 bottom electrode were deposited by radio-frequency (RF) sputtering onto Si(001) single-crystal substrates with SrTiO3/TiN buffer layers. Pb(Zr0.2Ti0.8)O3 (PZT) samples were shown to consist of a single perovskite phase and to have an (001) orientation. The orientation relationship was determined to be PZT(001)[110]∥LaNiO3(001)[110]∥SrTiO3 (001)[110]∥TiN(001)[110]∥Si(001)[110]. Atomic force microscope (AFM) measurements showed the PZT films to have smooth surfaces with a roughness of 1.15 nm. The microstructure of the multilayer was studied using transmission electron microscopy (TEM). Electrical measurements were conducted using both Pt and LaNiO3 as top electrodes. The measured remanent polarization P r and coercive field E c of the PZT thin film with Pt top electrodes were 23 μC/cm2 and 75 kV/cm, and were 25 μC/cm2 and 60 kV/cm for the PZT film with LaNiO3 top electrodes. No obvious fatigue after 1010 switching cycles indicated good electrical endurance of the PZT films using LaNiO3 electrodes, compared with the PZT film with Pt top electrodes showing a significant polarization loss after 108 cycles. These PZT films with LaNiO3 electrodes could be potential recording media for probe-based high-density data storage.

Determination of Heavy Metals in Meat, Intestine, Liver, Eggs, and Chicken Using Neutron Activation Analysis and Atomic Absorption Spectrometry

Energy Technology Data Exchange (ETDEWEB)

Surtipanti, S; Suwirma, S; Yumiarti, S; Mellawati, Yune [National Atomic Energy Agency, Jakarta (Indonesia), Center for the Application of Isotopes Radiation

1995-01-01

The elements As, Cd, Co, Cr, Fe, Hg, Ni, Pb, Sb, se and Zn in meat, intestine, and liver of cow and goat, as well as in broiler, local breed chicken and eggs have been determined using Neutron Activation Analysis and Atomic Absorption Spectrometry. Mercury was determined after being separated radiochemically. The results showed that concentration of the essential elements studied i.e. Cr, Cu, Fe, Zn, Co, and Ni were higher in liver and intestine than in the meat, but still in the normal range, while toxic elements As, Cd, and Pb were undetectable in all samples. (author). 8 refs., 6 tabs.

Determination of Heavy Metals in Meat, Intestine, Liver, Eggs, and Chicken Using Neutron Activation Analysis and Atomic Absorption Spectrometry

International Nuclear Information System (INIS)

Surtipanti, S.; Suwirma, S.; Yumiarti, S.; Mellawati, Yune

1995-01-01

The elements As, Cd, Co, Cr, Fe, Hg, Ni, Pb, Sb, se and Zn in meat, intestine, and liver of cow and goat, as well as in broiler, local breed chicken and eggs have been determined using Neutron Activation Analysis and Atomic Absorption Spectrometry. Mercury was determined after being separated radiochemically. The results showed that concentration of the essential elements studied i.e. Cr, Cu, Fe, Zn, Co, and Ni were higher in liver and intestine than in the meat, but still in the normal range, while toxic elements As, Cd, and Pb were undetectable in all samples. (author). 8 refs., 6 tabs

Studies of the 198Hg(d,d') and 198Hg(d,p) reactions

Science.gov (United States)

Diaz Varela, Alejandra; Garrett, P. E.; Rand, E. T.; Ball, G. C.; Bilstein, V.; Laffoley, A. T.; Maclean, A. D.; Svensson, C. E.; Faestermann, T.; Hertenberger, R.; Wirth, H.-F.

2017-09-01

Limits on the electric dipole moment (EDM) continue to decrease for 199Hg, the most stringent upper limit for a nuclear EDM to date. The experimental limit on the observed atomic EDM for 199Hg is converted to a limit on the nuclear EDM via a calculation of the Schiff moment, requiring knowledge of the nuclear structure of 199Hg. The E 3 and E 1 strength distributions to the ground state of 199Hg, and E 2 transitions amongst excited states, would be ideal information to further constrain 199Hg Schiff moment theoretical models. The high level density of 199Hg makes those determinations challenging, however the similar information can be obtained from exploring surrounding even-even Hg isotopes. As part of a campaign to study the Hg isotopes near 199Hg, two experiments, 198Hg(d,d') 198Hg and 198Hg(d,p)199Hg reaction were performed using the Q3D spectrograph at the Maier-Leibnitz Laboratory (MLL) at Garching, Germany. A 22 MeV deuterium beam was used to impinge a 198Hg32S target. The (d,d') reaction allows us to probe the desired E 2 and E 3 matrix elements, while the (d,p) reaction provides information on the neutron single-particle states of 199Hg.

Heavy metals and nutritional composition of some selected herbal ...

African Journals Online (AJOL)

saad

2012-09-20

Sep 20, 2012 ... Co, Cr, Hg, Mn, Ni, Pb and Zn) are toxic and lead to ... A stock standard solution of chloride and nitrate salts of zinc (Zn), copper (Cu), Iron (Fe), ..... of mouse neuronal excitability in culture of mouse hippocampus. J. physiol.

Source apportionment and health risk assessment of potentially toxic elements in road dust from urban industrial areas of Ahvaz megacity, Iran.

Science.gov (United States)

Najmeddin, Ali; Keshavarzi, Behnam; Moore, Farid; Lahijanzadeh, Ahmadreza

2017-10-28

This study investigates the occurrence and spatial distribution of potentially toxic elements (PTEs) (Hg, Cd, Cu, Mo, Pb, Zn, Ni, Co, Cr, Al, Fe, Mn, V and Sb) in 67 road dust samples collected from urban industrial areas in Ahvaz megacity, southwest of Iran. Geochemical methods, multivariate statistics, geostatistics and health risk assessment model were adopted to study the spatial pollution pattern and to identify the priority pollutants, regions of concern and sources of the studied PTEs. Also, receptor positive matrix factorization model was employed to assess pollution sources. Compared to the local background, the median enrichment factor values revealed the following order: Sb > Pb > Hg > Zn > Cu > V > Fe > Mo > Cd > Mn > Cr ≈ Co ≈ Al ≈ Ni. Statistical results show that a significant difference exists between concentrations of Mo, Cu, Pb, Zn, Fe, Sb, V and Hg in different regions (univariate analysis, Kruskal-Wallis test p matrix factorization model revealed that traffic-related emissions (43.5%) and steel industries (26.4%) were first two sources of PTEs in road dust, followed by natural sources (22.6%) and pipe and oil processing companies (7.5%). The arithmetic mean of pollution load index (PLI) values for high traffic sector (1.92) is greater than industrial (1.80) and residential areas (1.25). Also, the results show that ecological risk values for Hg and Pb in 41.8 and 9% of total dust samples are higher than 80, indicating their considerable or higher potential ecological risk. The health risk assessment model showed that ingestion of dust particles contributed more than 83% of the overall non-carcinogenic risk. For both residential and industrial scenarios, Hg and Pb had the highest risk values, whereas Mo has the lowest value.

Sources identification and pollution evaluation of heavy metals in the surface sediments of Bortala River, Northwest China.

Science.gov (United States)

Zhang, Zhaoyong; Juying, Li; Mamat, Zulpiya; QingFu, Ye

2016-04-01

The current study focused on the Bortala River - a typical inland river located in an oasis of arid area in northwestern China. The sediment and soil samples were collected from the river and drainage basin. Results showed that: (1) the particle size of the sand fraction of the sediments was 78-697 µm, accounting for 78.82% of the total samples; the average concentrations of eight heavy metals fell within the concentration ranges recommended by the Secondary National Standard of China, while the maximum concentrations of Pb, Cd, and Hg exceeded these standards; (2) results from multivariate statistical analysis indicated that Cu, Ni, As, and Zn originated primarily from natural geological background, while Cd, Pb, Hg and Cr in the sediments originated from human activities; (3) results of the enrichment factor analysis and the geo-accumulation index evaluation showed that Cd, Hg, and Pb were present in the surface sediments of the river at low or partial serious pollution levels, while Zn, Cr, As, Ni, and Cu existed at zero or low pollution levels; (4) calculation of the potential ecological hazards index showed that among the eight tested heavy metals, Cd, Pb, Hg, and Cr were the main potential ecological risk factors, with relative contributions of 25.43%, 22.23%, 21.16%, and 14.87%, respectively; (5) the spatial distribution of the enrichment factors (EF(S)), the Geo-accumulation index (I(geo)), and the potential ecological risk coefficient (E(r)(i)) for eight heavy metals showed that there was a greater accumulation of heavy metals Pb, Cd, and Hg in the sediments of the central and eastern parts of the river. Results of this research can be a reference for the heavy metals pollution prevention, the harmony development of the ecology protection and the economy development of the oases of inland river basin of arid regions of China, Central Asia and also other parts of the world. Copyright © 2015 Elsevier Inc. All rights reserved.

Heavy metal content (Cd, Ni, Cr and Pb) in soil amendment with a low polluted biosolid

Science.gov (United States)

Gomez Lucas, Ignacio; Lag Brotons, Alfonso; Navarro-Pedreño, Jose; Belén Almendro-Candel, Maria; Jordán, Manuel M.; Bech, Jaume; Roca, Nuria

2016-04-01

The progressively higher water quality standards in Europe has led to the generation of large quantities of sewage sludge derived from wastewater treatment (Fytili and Zabaniotou 2008). Composting is an effective method to minimize these risks, as pathogens are biodegraded and heavy metals are stabilized as a result of organic matter transformations (Barker and Bryson 2002; Noble and Roberts 2004). Most of the studies about sewage sludge pollution are centred in medium and high polluted wastes. However, the aim of this study was to assess the effects on soil heavy metal content of a low polluted sewage sludge compost in order to identify an optimal application rate based in heavy metal concentration under a period of cultivation of a Mediterranean horticultural plant (Cynara carducnculus). The experiment was done between January to June: rainfall was 71 mm, the volume of water supplied every week was 10.5 mm, mean air temperatures was 14.2, 20.4 (maximum), and 9.2◦C (minimum). The soil was a clay-loam anthrosol (WRB 2006). The experimental plot (60 m2) was divided into five subplots with five treatments corresponding to 0, 2, 4, 6, and 8 kg compost/m2. Three top-soil (first 20 cm) samples from each treatment were taken (January, April and June) and these parameters were analysed: pH, electrical conductivity, organic matter and total content of heavy metals (microwave acid digestion followed by AAS-spectrometry determination). The results show that sewage sludge compost treatments increase the organic matter content and salinity (electrical conductivity of the soils) and diminish the pH. Cd and Ni total content in top-soil was affected and both slightly reduce their concentration. Pb and Cr show minor changes. In general, the application of this low polluted compost may affect the mobility of Cd and Ni due to the pH modification and the water added by irrigation along time but Pb and Cr remain their content in the top-soil. References Barker, A.V., and G.M. Bryson

Determining baseline element composition of lichens. I. Parmelia sulcata at Theodore Roosevelt national park, North Dakota

Science.gov (United States)

Gough, L.P.; Severson, R.C.; Jackson, L.L.

1988-01-01

Element-concentration baselines are given for Parmelia sulcata and associated soils. Parmelia chlorochroa was found sporadically and therefore only representative concentration ranges are reported for this species. Element data include (1) for lichens; Al, As, Ba, B, Ca, Cr, Cu, Fe, Hg, Mn, Ni, P, Sr, S, Ti, V, Y, and Zn; and (2) for soils: Al, Ba, Be, Ca, Cs, Cr, Cu, Fe, Hg, Mg, Mn, Ni, Nb, P, Pb, Sr, S, Ti, V, Y, and Zn. Very little (usually 7.2 km); thus, P sulcata is, in general, chemically similar throughout the park. This same uniformity was found for soil geochemistry. Numerous samples collected at close intervals would be required, therefore, to produce detailed element-concentration maps for P. sulcata and soils. No instances of elemental phytotoxic conditions were found; however, P. sulcata apparently possesses large concentrations of Ba, Cu, Fe, Pb, S, V, and possibly Zn.

Ion Exchange Properties of a Terpolymer Resin Derived from 2, 4-Dihydroxybenzaldehyde, Oxamide and Formaldehyde

Directory of Open Access Journals (Sweden)

M. V. Tarase

2009-01-01

Full Text Available Terpolymer resins (2,4-DHBOF were synthesized by the condensation of 2,4-dihydroxybenzaldehyde and oxamide with formaldehyde in the presence of hydrochloric acid as catalyst, proved to be selective chelation ion exchange terpolymer resins for certain metals. Chelation ion exchange properties of these polymers were studied for Fe+3, Cu+2, Hg+2, Cd+2, Co+2, Zn+2, Ni+2 and Pb+2 ions. A batch equilibrium method was employed in the study of the selectivity of the distribution of a given metal ions between the polymer sample and a solution containing the metal ion. The study was carried out over a wide pH range and in a media of various ionic strengths. The polymer showed a higher selectivity for Fe+3, Cd+2 and Co+2 ions than for Cu+2, Hg+2, Zn+2, Ni+2 and Pb+2 ions.

Metal concentrations in demersal fish species from Santa Maria Bay, Baja California Sur, Mexico (Pacific coast).

Science.gov (United States)

Jonathan, M P; Aurioles-Gamboa, David; Villegas, Lorena Elizabeth Campos; Bohórquez-Herrera, Jimena; Hernández-Camacho, Claudia J; Sujitha, S B

2015-10-15

Concentrations of 11 trace metals (Fe, Mn, Cr, Cu, Ni, Co, Pb, Zn, Cd, As, Hg) in 40 fish species from Santa Maria Bay, Baja California Sur, Mexico, the strategically important area for marine mammals and organisms were analyzed. Based on their concentrations the ranking of metals Fe>Zn>Ni>Cr>Mn>Pb>Cu>Co>As>Cd>Hg suggests that organism size, metabolism and feeding habits are correlated with metal concentrations. Local geological formations affect the concentrations of different metals in the aquatic environment and are subsequently transferred to fishes. The correlation analysis suggests that metabolism and nurturing habits impact the concentration of metals. Concentrations of Fe and Mn appear to be influenced by scavenging and absorption processes, which vary by species. The considerable variability in the metal concentrations obtained in different species underscores the importance of regular monitoring. Copyright © 2015 Elsevier Ltd. All rights reserved.

46 CFR 53.12-1 - General (modifies HG-600 through HG-640).

Science.gov (United States)

2010-10-01

... 46 Shipping 2 2010-10-01 2010-10-01 false General (modifies HG-600 through HG-640). 53.12-1... HEATING BOILERS Instruments, Fittings, and Controls (Article 6) § 53.12-1 General (modifies HG-600 through HG-640). (a) The instruments, fittings and controls for heating boilers shall be as indicated in HG...

Propyl phthalimide-modified thiacalixphenyl[4]arene as a “turn on” chemosensor for Hg(II) ions

Energy Technology Data Exchange (ETDEWEB)

Modi, Krunal; Panchal, Urvi; Mehta, Viren; Panchal, Manthan; Kongor, Anita; Jain, V.K., E-mail: drvkjain@hotmail.com

2016-11-15

Thiacalixphenyl[4]arene tetra N-(3-propyl) phthalimide (TPTN3PPh), a novel thiacalixarene bearing a N-(3-bromopropyl) phthalimide group, was synthesized and characterized by Electrospray Ionization Mass Spectrometry (ESI-MS) and NMR. The ability of TPTN3PPh to recognize the cations Fe(III), Cu(II), Cd(II), Zn(II), Cr(II), Ca(II), Co(II), Mg(II), Ag(I), Pb(II), Sr(II), Hg (II), Th(II), Ba(II), Bi(II), K(I), and Na(I) was evaluated. Only Hg(II) was selectively and sensitively detected using a spectrofluorimetric method, with a detection limit as low as 3.10×10{sup −9} M. Analysis of the binding behavior of TPTN3PPh with Hg(II) revealed 1:2 complex formation. Real sample analysis detected nano levels of mercury ions in a waste water samples.

Shedding light on the mercury mass discrepancy by weighing Hg52+ ions in a Penning trap

International Nuclear Information System (INIS)

Fritioff, T.; Bluhme, H.; Schuch, R.; Bergstroem, I.; Bjoerkhage, M.

2003-01-01

In their nuclear tables Audi and Wapstra have pointed out a serious mass discrepancy between their extrapolated values for the mercury isotopes and those from a direct measurement by the Manitoba group. The values deviate by as much as 85 ppb from each other with claimed uncertainties of about 16 and 7 ppb, respectively. In order to decide which values are correct the masses of the 198 Hg and 204 Hg isotopes have been measured in the Stockholm Penning trap mass spectrometer SMILETRAP using 52+ ions. This charge state corresponds to a filled Ni electron configuration for which the electron binding energy can be accurately calculated. The mass values obtained are 197.966 768 44(43) u for 198 Hg and 203.973 494 10(39) u for 204 Hg. These values agree with those measured by the Manitoba group, with a 3 times lower uncertainty. This measurement was made possible through the implementation of a cooling technique of the highly charged mercury ions during charge breeding in the electron beam ion source used for producing the Hg 52+ ions

Novel chelating resin with cyanoguanidine group: Useful recyclable materials for Hg(II) removal in aqueous environment

International Nuclear Information System (INIS)

Ma Xiaojie; Li Yanfeng; Ye Zhengfang; Yang Liuqing; Zhou Lincheng; Wang Liyuan

2011-01-01

A novel chelating resin containing cyanoguanidine moiety has been successfully prepared by the functionalizing reaction of a macroporous bead based on chloromethylated copolymer of styrene-divinylbenzene (CMPS) with dicyandiamide (DCDA) in the presence of phase transfer catalyst. The Fourier transform-infrared spectra (FT-IR) and scanning electron microscopy (SEM) were employed in the characterization of the resulting chelating resin, meanwhile, the adsorption properties of the resin for Hg(II) were investigated by batch and column methods. The results indicated that the resin displayed a marked advantage in Hg(II) binding capacity, and the saturated adsorption capacity estimated from the Langmuir model was dramatically up to 1077 mg g -1 at 45 deg. C. Furthermore, it was found that the resin was able to selectively separate Hg(II) from multicomponent solutions with Zn(II), Cu(II), Pb(II) and Mg(II). The desorption process of Hg(II) was tested with different eluents and the ratio of the highest recovery reached to 96% under eluting condition of 1 M HCl + 10% thiourea. Consequently, the resulting chelating resin would provide a potential application for treatment process of Hg(II) containing wastewater.

Soil Cd, Cr, Cu, Ni, Pb and Zn sorption and retention models using SVM: Variable selection and competitive model.

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González Costa, J J; Reigosa, M J; Matías, J M; Covelo, E F

2017-09-01

The aim of this study was to model the sorption and retention of Cd, Cu, Ni, Pb and Zn in soils. To that extent, the sorption and retention of these metals were studied and the soil characterization was performed separately. Multiple stepwise regression was used to produce multivariate models with linear techniques and with support vector machines, all of which included 15 explanatory variables characterizing soils. When the R-squared values are represented, two different groups are noticed. Cr, Cu and Pb sorption and retention show a higher R-squared; the most explanatory variables being humified organic matter, Al oxides and, in some cases, cation-exchange capacity (CEC). The other group of metals (Cd, Ni and Zn) shows a lower R-squared, and clays are the most explanatory variables, including a percentage of vermiculite and slime. In some cases, quartz, plagioclase or hematite percentages also show some explanatory capacity. Support Vector Machine (SVM) regression shows that the different models are not as regular as in multiple regression in terms of number of variables, the regression for nickel adsorption being the one with the highest number of variables in its optimal model. On the other hand, there are cases where the most explanatory variables are the same for two metals, as it happens with Cd and Cr adsorption. A similar adsorption mechanism is thus postulated. These patterns of the introduction of variables in the model allow us to create explainability sequences. Those which are the most similar to the selectivity sequences obtained by Covelo (2005) are Mn oxides in multiple regression and change capacity in SVM. Among all the variables, the only one that is explanatory for all the metals after applying the maximum parsimony principle is the percentage of sand in the retention process. In the competitive model arising from the aforementioned sequences, the most intense competitiveness for the adsorption and retention of different metals appears between

Assessment of heavy metal pollution, spatial distribution and origin in agricultural soils along the Sinú River Basin, Colombia.

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Marrugo-Negrete, José; Pinedo-Hernández, José; Díez, Sergi

2017-04-01

The presence of metals in agricultural soils from anthropogenic activities such as mining and agricultural use of metals and metal-containing compounds is a potential threat for human health through the food chain. In this study, the concentration of heavy metals in 83 agricultural soils irrigated by the Sinú River, in northern Colombia, affected by mining areas upstream and inundated during seasonal floods events were determined to evaluate their sources and levels of pollution. The average concentrations of Cu, Ni, Pb, Cd, Hg and Zn were 1149, 661, 0.071, 0.040, 0.159 and 1365mg/kg respectively and exceeded the world normal averages, with the exception of Pb and Cd. Moreover, all values surpassed the background levels of soils in the same region. Soil pollution assessment was carried out using contamination factor (CF), enrichment factor (EF), geoaccumulation index (Igeo) and a risk assessment code (RAC). According to these indexes, the soils show a high degree of pollution of Ni and a moderate to high contamination of Zn and Cu; whereas, Pb, Cd and Hg present moderate pollution. However, based on the RAC index, a low environmental risk is found for all the analysed heavy metals. Multivariate statistical analyses, principal component and cluster analyses, suggest that soil contamination was mainly derived from agricultural practices, except for Hg, which was caused probably by atmospheric and river flow transport from upstream gold mining. Finally, high concentrations of Ni indicate a mixed pollution source from agricultural and ferronickel mining activities. Copyright © 2017 Elsevier Inc. All rights reserved.

Arsenic and Other Elemental Concentrations in Mushrooms from Bangladesh: Health Risks

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Md Harunur Rashid

2018-05-01

Full Text Available Mushroom cultivation has been increasing rapidly in Bangladesh. Arsenic (As toxicity is widespread in the world and Bangladesh faces the greatest havoc due to this calamity. Rice is the staple food in Bangladesh and among all the crops grown, it is considered to be the main cause of As poisoning to its population after drinking water. Consequently, rice straw, an important growing medium of mushrooms in Bangladesh, is known to have high As content. The objective of this study was, therefore, to determine the concentrations of As in mushrooms cultivated in Bangladesh and to assess the health risk as well. It also considered other elements, including Cd, Cr, Co, Cu, Pb, Mn, Hg, Ni, and Zn concentrations in mushrooms from Bangladesh. The mean concentrations (mg/kg of As, Cd, Cr, Co, Cu, Pb, Mn, Hg, Ni, and Zn in mushrooms were 0.51, 0.38, 0.28, 0.01, 13.7, 0.31, 11.7, 0.12, 0.28, and 53.5, respectively. Based on the dietary intake of mushrooms, the weekly intakes of As, Cd, Cr, Co, Cu, Pb, Mn, Hg, Ni, and Zn from mushrooms for adults were 0.0042, 0.0030, 0.0024, 0.0001, 0.1125, 0.0019, 0.1116, 0.0011, 0.0023, and 0.4734 mg, respectively. Due to the low concentrations of As and other trace elements observed in mushrooms from Bangladesh, as well as relatively lower consumption of this food in people’s diet, it can be inferred that consumption of the species of mushrooms analysed will cause no toxicological risk.

Characterization and origin of organic and inorganic pollution in urban soils in Pisa (Tuscany, Italy).

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Cardelli, Roberto; Vanni, Giacomo; Marchini, Fausto; Saviozzi, Alessandro

2017-10-12

We assessed the quality of 31 urban soils in Pisa by analyzing total petroleum hydrocarbons (TPHs), Cd, Cr, Cu, Hg, Mn, Ni, Pb, Zn, and the platinum group elements (PGEs). The risk was evaluated by the geological accumulation index (I geo ) and the enrichment factor (EF). Results were compared with those obtained from a non-urban site and with the quantitative limits fixed by Italian legislation. In nearly all the monitored sites, the legal limit for TPH of 60 mg/kg in residential areas was exceeded, indicating widespread and intense pollution throughout the entire city area. The I geo indicated no Cd, Cu, Mn, Ni, and Zn pollution and minimal Pb and Cr pollution due to anthropogenic enrichment. Legal Hg and Zn limits of 1 and 150 mg/kg, respectively, were exceeded in about 20% of sites; Cd (2 mg/kg), Cr (150 mg/kg), and Cu (120 mg/kg) in only one site; and the Ni legal limit of 120 mg/kg was never exceeded. Some urban soils showed a higher Hg level than the more restrictive legal limit of 5 mg/kg concerning areas for industrial use. Based on the soluble, exchangeable, and carbonate-bound fractions, Mn and Zn showed the highest mobility, suggesting a more potential risk of soil contamination than the other metals. The TPH and both Cr and Hg amounts were not correlated with any of the other monitored metals. The total contents of Cd, Pb, Zn, and Cu in soils were positively correlated with each other, suggesting a common origin from vehicular traffic. The PGE values (Pt and Pd) were below the detection limits in 75%-90% of the monitored areas, suggesting that their accumulation is at an early stage.

Study on the prediction of soil heavy metal elements content based on visible near-infrared spectroscopy

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Liu, Jinbao; Zhang, Yang; Wang, Huanyuan; Du, Yichun

2018-06-01

The estimation of soils heavy metal content can reflect the impending surroundings of surface, which lays theoretical foundation for using covered vegetation to monitor environment and investigate resource. In this study, the contents of Cr, Mn, Ni, Cu, Zn, As, Cd, Hg and Pb in 44 soil samples were collected from Fufeng County, Yangling County and Wugong County, Shaanxi Province and were used as data sources. ASD FieldSpec HR (350-2500 nm), and then the NOR, MSC and SNV of the reflectance were pretreated, the first deviation, second deviation and reflectance reciprocal logarithmic transformation were carried out. The optimal spectroscopy estimation model of nine heavy metal elements of Cr, Mn, Ni, Cu, Zn, As, Cd, Hg and Pb was established by regression method. Comparing the diffuse reflectance characteristics of different heavy metal contents and the effect of different pretreatment methods on the establishment of soil heavy metal spectral inversion model. The results of chemical analysis show that there was a serious Hg pollution in the study area, and the Cd content was close to the critical value. The results show that: (1) NOR, MSC and SNV were adopted for the acquisition of visible near-infrared. Combining differential transformation can improve the information of heavy metal elements in the soil, and use the correlation band energy Significantly improve the stability and predictability of the model. (2) The modeling accuracy of the optimal model of nine heavy metal spectra of Cr, Mn, Ni, Cu, Zn, As, Cd, Hg and Pb by PLSR method were 0.70, 0.79, 0.69, 0.81, 0.86, 0.58, 0.55, 0.99, 0.62. (3) The optimal estimation model of different elements using different treatment methods has better stability and higher precision, and can realize the rapid prediction of nine kinds of heavy metal elements in this region.

Quadrupole moments of the 12+ isomers in 188Hg and 190Hg

International Nuclear Information System (INIS)

Dracoulis, G.D.; Lonnroth, T.; Vajda, S.; Dafni, E.; Schatz, G.

1984-01-01

The electric quadrupole interaction of the 12 + isomers in 188 Hg and 190 Hg has been measured in solid Hg. The quadrupole moments deduced, vertical strokeQ[ 188 Hg(12 + )]vertical stroke = 91(11) e fm 2 and vertical strokeQ[ 190 Hg(12 + )]vertical stroke = 117(14) e fm 2 suggest a possible change in γ-deformation due to the rotation alignment of the isub(13/2) quasi-neutrons. The temperature dependence of the electric field gradient tensor in Hg was also determined. (orig.)

Tracing aquatic bioavailable Hg in three different regions of China using fish Hg isotopes.

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Liu, Cheng-Bin; Hua, Xiu-Bing; Liu, Hong-Wei; Yu, Ben; Mao, Yu-Xiang; Wang, Ding-Yong; Yin, Yong-Guang; Hu, Li-Gang; Shi, Jian-Bo; Jiang, Gui-Bin

2018-04-15

To trace the most concerned bioavailable mercury (Hg) in aquatic environment, fish samples were collected from three typical regions in China, including 3 rivers and 1 lake in the Tibetan Plateau (TP, a high altitude background region with strong solar radiation), the Three Gorges Reservoir (TGR, the largest artificial freshwater reservoir in China), and the Chinese Bohai Sea (CBS, a heavily human-impacted semi-enclosed sea). The Hg isotopic compositions in fish muscles were analyzed. The results showed that anthropogenic emissions were the main sources of Hg in fish from TGR and CBS because of the observed negative δ 202 Hg and positive Δ 199 Hg in these two regions (TGR, δ 202 Hg: - 0.72 to - 0.29‰, Δ 199 Hg: 0.15 - 0.52‰; CBS, δ 202 Hg: - 2.09 to - 0.86‰, Δ 199 Hg: 0.07 - 0.52‰). The relatively higher δ 202 Hg and Δ 199 Hg (δ 202 Hg: - 0.37 - 0.08‰, Δ 199 Hg: 0.50 - 1.89‰) in fish from TP suggested the insignificant disturbance from local anthropogenic activities. The larger slopes of Δ 199 Hg/Δ 201 Hg in fish from TGR (1.29 ± 0.14, 1SD) and TP (1.25 ± 0.06, 1SD) indicated methylmercury (MeHg) was produced and photo-reduced in the water column before incorporation into the fish. In contrast, the photoreduction of Hg 2+ was the main process in CBS (slope of Δ 199 Hg/Δ 201 Hg: 1.06 ± 0.06, 1SD). According to the fingerprint data of Hg isotopes, the most important source for aquatic bioavailable Hg in TP should be the long-range transported Hg, contrasting to the anthropogenic originated MeHg from surface sediments and runoffs in TGR and inorganic Hg from continental inputs in CBS. Therefore, the isotopic signatures of Hg in fish can provide novel clues in tracing sources and behaviors of bioavailable Hg in aquatic systems, which are critical for further understanding the biogeochemical cycling of Hg. Copyright © 2017 Elsevier Inc. All rights reserved.