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Sample records for chalcophile elements hg

  1. 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...... growth of phytoplankton in surface water layers and with sedimentation of lifeless organisms and suspended particles in near-bottom layers. Average concentrations of Pb and Cd in the water column were more than the average value for water of lakes of the taiga zone. Pollution of Lake Umbozero led......Investigations of Lake Umbozero, the second largest and the deepest lake of the Murmansk Region, were carried out to detect and define biogeochemical patterns of distribution of the chalcophile elements (Hg, Cd, Pb, As) in water, sediments and organs and tissues of whitefishes. Lake Umbozero...

  2. Chalcophile element partitioning into magmatic sulphides: the effect of silicate melt composition

    Science.gov (United States)

    Kiseeva, Kate; Wood, Bernard

    2016-04-01

    Partitioning of many elements between sulphide and silicate melts is a function of the FeO content of the silicate liquid (Kiseeva and Wood, 2013). The theoretical relationship is a linear one between LogDM (DM=[M]sulph/[M]sil) and -log[FeO] with a slope of n/2, where n is the valency of trace element M. In practice we find that the slope deviates from the theoretical one because of the presence of oxygen in the sulphide. In our recent study we investigated the effects of sulphide composition and temperature on chalcophile element partitioning between sulphide and silicate liquids (Kiseeva and Wood, 2015). We have concluded that partitioning of most chalcophile elements is a strong function of the oxygen (or FeO) content of the sulphide. As expected, lithophile elements partition more strongly into sulphide as its oxygen content increases, while chalcophile elements enter sulphide less readily with increasing oxygen. The effect of Ni and Cu content of sulphide is significantly smaller than the effect of oxygen, while the effects of temperature are large only for a number of elements (such as Ni, Cu, Ag). In this study we show that in addition to the effect of sulphide composition, for certain elements the effect of silicate melt composition on sulphide/silicate partitioning can be quite large. For instance, within the range of NBO/T between 0.5 and 2 the DTlsulph/sil changes in order of magnitude. For the elements, like Pb, partition coefficient does not seem to change much with the silicate melt composition, while for Sb the effect of the silicate melt composition on D is a factor of 3. Partitioning of chalcophile elements into more evolved, alkali-rich and felsic magmas is estimated to be very different from the partitioning into basaltic melts, mainly due to the strong effects of temperature and alkali components. Although it is highly likely that sulphide is in solid form at liquidus temperatures for dacite and rhyolite and thus the partitioning of chalcophile

  3. Mantle-crust differentiation of chalcophile elements in the oceanic lithosphere

    Science.gov (United States)

    Ciążela, J.; Dick, H. J.; Koepke, J.; Kuhn, T.; Muszynski, A.; Kubiak, M.

    2014-12-01

    The chalcophile elements, as associated with sulfides, are believed mainly from the study of ophiolites to be generally enriched in the upper mantle, but depleted by magmatic processes in the lower and upper ocean crust. However, studies of some orogenic lherzolites suggest a copper depletion of peridotites in relation to the primitive mantle, suggesting that a portion of the sulfides is melted during decompression and incorporated into the ascending magmas. The rarity of abyssal peridotites and the high degree of their alteration have not allowed these results to be verified in situ in the oceans.Here, we present the first complete study of chalcophile elements based on a suite of rocks from an oceanic core complex (OCC), the Kane Megamullion at 22°30'N at the Mid-Atlantic Ridge. OCCs provide large exposures of mantle and lower crustal rocks on the seafloor on detachment fault footwalls at slow and ultraslow spreading ridges. The Kane Megamullion is one of the best sampled OCCs in the world, with 1342 rocks from 28 dredge sites and 14 dives. We have made XRF, TD-MS and INAA analyses of 129 representative peridotites, gabbroic rocks, diabases and basalts. Our results suggest a depletion of some peridotites in relation to the primitive mantle (28 ppm Cu). Dunites, troctolites and olivine gabbros are relatively enriched in chalcophile elements. The amount of sulfides decreases gradually with progressive differentiation, reaching a minimum in gabbronorites and diabases. The highest bulk abundance of chalcophile elements in our sample suite was observed in dunites (up to ~ 300 ppm Cu in several samples) and a contact zone between residual peridotite and a mafic vein (294 ppm Cu). Plagioclase-bearing harzburgites, generally formed by late-stage melt impregnation in the mantle, are typically more enriched in Cu than unimpregnated residual peridotites. For these reasons, our initial results indicate sulfide melting during mantle melting, and their local precipitation in

  4. Bulk compositions of metallic Fe-Ni of chondrites: Constraints on fractionation of siderophile and chalcophile elements

    Institute of Scientific and Technical Information of China (English)

    XU Lin; LIN Yangting; WANG Shijie; OUYANG Ziyuan

    2009-01-01

    Bulk compositions of metallic Fe-Ni from two equilibrated ordinary chondrites, Jilin (H5) and Anlong (H5), and two unequilibrated ones, GRV 9919 (L3) and GRV 021603 (H3), were analyzed by inductively coupled plasma mass spectrometry (ICP-MS). The CI-, Co-normalized abundances of siderophile and chalcophile elements of metallic Fe-Ni from the unequilibrated ordinary chondrites correlate with 50% condensation temperatures (i.e., volatility) of the elements. The refractory siderophile elements (i.e., platinum group elements, Re), Au, Ni and Co show a flat pattern (1.01(CI Co-normalized), while moderate elements (As, Cu, Ag, Ga, Ge, Zn) decrease with volatility from 0.63(CI (Co-normalized, As) to 0.05(CI (Co-normalized, Zn). Cr and Mn show deficit relative to the trend, probably due to their main partition in silicates and sulfides (nonmagnetic). Metallic Fe-Ni from the equilibrated ordinary chondrites shows similar patterns, except for strong deficit of Cr, Mn, Ag and Zn. It is indicated that these elements were almost all partitioned into silicates and/or sulfides during thermal metamorphism. The similar deficit of Cr, Mn, Ag and Zn was also found in iron meteorites.Our analyses demonstrate similar behaviors of W and Mo as refractory siderophile elements during condensation of the solar nebula, except for slight depletion of Mo in the L3 and H5 chondrites. The Mo-depletion of metallic Fe-Ni from GRV 9919 (L3) relative to GRV 021603 (H3) could be due to a more oxidizing condition of the former than the latter in the solar nebula. In contrast, the Mo-depletion of the metallic Fe-Ni from the H5 chondrites may reflect partition of Mo from metal to silicates and/or sulfides during thermal metamorphism in the asteroidal body.

  5. Using chalcophile elements to constrain crustal contamination and xenolith-magma interaction in Cenozoic basalts of eastern China

    Science.gov (United States)

    Zeng, Gang; Huang, Xiao-Wen; Zhou, Mei-Fu; Chen, Li-Hui; Xu, Xi-Sheng

    2016-08-01

    Continental basalts have complicated petrogenetic processes, and their chemical compositions can be affected by multi-staged geological evolution. Compared to lithophile elements, chalcophile elements including Ni, platinum-group elements (PGEs) and Cu are sensitive to sulfide segregation and fractional crystallization during the evolution of mantle-derived magmas and can provide constraints on the genesis of continental basalts. Cenozoic intra-continental alkaline basalts in the Nanjing basaltic field, eastern China, include high-Ca and low-Ca varieties. All these basalts have poor PGE contents with Ir ranging from 0.016 ppb to 0.288 ppb and high Cu/Pd ratios from 0.7 × 105 to 4.7 × 105 (5.7 × 103 for DMM), indicating that they were derived from sulfide-saturated mantle sources with variable amounts of residual sulfide during melting or might undergo an early-sulfide segregation in the mantle. Relatively high Cu/Pd ratios along with high Pd concentrations for the high-Ca alkaline basalts indicate an additional removal of sulfide during magma ascent. Because these basalts have high, variable Pd/Ir ratios (2.8-16.8) with low Ce/Pb (9.9-19.7) ratios and εNd values (+ 3.6-+6.4), crustal contamination is proposed to be a potential process to induce the sulfide saturation and removal. Significantly increased Pd/Ir ratios for few high-Ca basalts can be explained by the fractionation of laurite or Ru-Os-Ir alloys with olivine or chromite. For low-Ca alkaline basalts, their PGE contents are well correlated with the MgO, Sc contents, incompatible element ratios (Lu/Hf, Na/Ti and Ca/Al) and Hf isotopes. Good correlations are also observed between Pd/Ir (or Rh/Ir) and Na/Ti (or Ca/Al) ratios. Variations of these elemental ratios and Hf isotopes is previously documented to be induced by the mixing of peridotite xenolith-released melts during ascent. Therefore, we suggest that such xenolith-magma interaction are also responsible for the variable PGE compositions of low

  6. Element spots in HgMn stars

    OpenAIRE

    Korhonen, Heidi

    2013-01-01

    A fraction of late B-type stars, the so-called HgMn stars, exhibit enhanced absorption lines of certain chemical elements, notably Hg and Mn, combined with an underabundance of He. For about a decade now the elements with anomalously high abundances in HgMn stars are known to be distributed inhomogeneously over the stellar surface. Temporal evolution of these elemental spots have been reported in a few HgMn stars, first secular evolution of the mercury spots in alpha And, and recently also a ...

  7. Element spots in HgMn stars

    CERN Document Server

    Korhonen, Heidi

    2013-01-01

    A fraction of late B-type stars, the so-called HgMn stars, exhibit enhanced absorption lines of certain chemical elements, notably Hg and Mn, combined with an underabundance of He. For about a decade now the elements with anomalously high abundances in HgMn stars are known to be distributed inhomogeneously over the stellar surface. Temporal evolution of these elemental spots have been reported in a few HgMn stars, first secular evolution of the mercury spots in alpha And, and recently also a fast evolution of yttrium and strontium spots in HD 11753. The fast evolution of spots in HD 11753 is combined with a slower change in the overall abundance of the affected elements. In this paper I review what is known of elemental spots in HgMn stars and their secular and fast temporal evolution.

  8. Element spots in HgMn stars

    Science.gov (United States)

    Korhonen, H.

    2014-11-01

    A fraction of late B-type stars, the so-called HgMn stars, exhibit enhanced absorption lines of certain chemical elements, notably Hg and Mn, combined with an underabundance of He. For about a decade it has been known that the elements with anomalously high abundances in HgMn stars are distributed inhomogeneously over the stellar surface. Observation of the temporal evolution of those spots has been reported in a few HgMn stars, first of a secular evolution of the mercury spots in α And, and more recently of a fast evolution of yttrium and strontium spots in HD 11753. The fast evolution of spots in HD 11753 is combined with a slower change in the overall abundance of the elements affected. In this paper I review what is known about these ``elemental spots'' in HgMn stars and their secular and fast temporal evolution.

  9. Should I Stay or Should I Go? The Effects of Weathering on Siderophile and Chalcophile Element Mobility in Mantle-Derived Sulfides

    Science.gov (United States)

    Harvey, J.; Warren, J. M.; Humayun, M.; Walshaw, R.

    2015-12-01

    Jason Harvey1,2, Jessica M Warren2, Munir Humayun3, Richard D Walshaw1 School of Earth and Environment, University of Leeds, Leeds, UK Dept. of Earth and Environmental Sciences, Stanford University, Stanford CA, USA National High Magnetic Field Laboratory, Florida State University, Tallahassee FL, USA Peridotite xenoliths possess lower abundances of S and Os than peridotite massifs. This has been attributed to the ingress of meteoric water, which oxidizes sulfide, removing sulfur as soluble sulfate, while volatilizing Os to its more mobile OsO4 form[1]. Selenium is considered to be less mobile than S under oxidizing conditions[2]. This assumption was challenged recently when peridotite xenoliths from Kilbourne Hole were analysed for bulk-rock PGE-S-Se-Te-Re abundances[3]. The sulfides they contained had clearly experienced varying degrees of oxidation to Fe-oxyhydroxides, but yielded chondritic bulk-rock Se/S, consistent with values found in massif peridotites. This requires that Se is mobile during supergene weathering, otherwise supra-chondritic Se/S would be generated. Here, we present the results of a LA-ICP-MS investigation into the highly siderophile element (HSE) and chalcophile element abundances of ca. 20 BMS grains from one of the same Kilbourne Hole xenoliths of the former bulk-rock study[3]. Osmium abundance and Os/Ir (where not fractionated by high temperature processes involving sulfide) are well correlated with both Se and S across a wide range of oxidation. Other platinum group elements (Ir, Ru, Rh, Pt, Pd) show no obvious signs of mobility with decreasing S (or Se) abundance. The positive co-variation between S and Se for a wide range of S abundance adds credence to the theory that Se may also be mobile during the oxidative breakdown of peridotite- hosted sulfides. Using Se as a proxy for S abundance in peridotite xenoliths should therefore be used with care. Moreover, the attribution of chondritic Se/S in peridotites to bulk-earth compositions may

  10. New technique for quantification of elemental hg in mine wastes and its implications for mercury evasion into the atmosphere

    Science.gov (United States)

    Jew, A.D.; Kim, C.S.; Rytuba, J.J.; Gustin, M.S.; Brown, Gordon E.

    2011-01-01

    Mercury in the environment is of prime concern to both ecosystem and human health. Determination of the molecular-level speciation of Hg in soils and mine wastes is important for understanding its sequestration, mobility, and availability for methylation. Extended X-ray absorption fine structure (EXAFS) spectroscopy carried out under ambient P-T conditions has been used in a number of past studies to determine Hg speciation in complex mine wastes and associated soils. However, this approach cannot detect elemental (liquid) mercury in Hg-polluted soils and sediments due to the significant structural disorder of liquid Hg at ambient-temperature. A new sample preparation protocol involving slow cooling through the crystallization temperature of Hg(0) (234 K) results in its transformation to crystalline ??-Hg(0). The presence and proportion of Hg(0), relative to other crystalline Hg-bearing phases, in samples prepared in this way can be quantified by low-temperature (77 K) EXAFS spectroscopy. Using this approach, we have determined the relative concentrations of liquid Hg(0) in Hg mine wastes from several sites in the California Coast Range and have found that they correlate well with measured fluxes of gaseous Hg released during light and dark exposure of the same samples, with higher evasion ratios from samples containing higher concentrations of liquid Hg(0). Two different linear relationships are observed in plots of the ratio of Hg emission under light and dark conditions vs % Hg(0), corresponding to silica-carbonate- and hot springs-type Hg deposits, with the hot springs-type samples exhibiting higher evasion fluxes than silica-carbonate type samples at similar Hg(0) concentrations. Our findings help explain significant differences in Hg evasion data for different mine sites in the California Coast Range. ?? 2011 American Chemical Society.

  11. Use of Hg-Electroplated-Pt Ultramicroelectrode for Determining Elemental Sulphur in Naphtha Samples

    Directory of Open Access Journals (Sweden)

    Carlos Eduardo de Andrade

    2012-01-01

    Full Text Available This paper describes the applicability of a Hg-electroplated-Pt ultramicroelectrode in the quantification of elemental sulphur in naphtha samples by square-wave voltammetry. A reproducible deposition methodology was studied and is reported in this paper. This methodology is innovative and relies on the quality of the mercury stock solution to obtain reproducible surfaces required for the analytical methodology. All analyses were performed using a Hg-electroplated-Pt ultramicroelectrode (Hg-Pt UME due to the low sensibility of such devices to ohmic drops in resistive solutions. The responses of the peak areas in voltammetric experiments were linear in all of the range studied. The method developed here is accurate and reproducible, with a detection limit of 0.010 mg L−1 and a good recovery range for both standard solutions of elemental sulphur (85 to 99% and real naphtha sample (79%. These results attest to the potential for the application of this electroanalytical methodology in determining elemental sulphur in naphtha samples containing mercaptans and disulphides.

  12. Investigation of the E2 and E3 matrix elements in 200Hg using inelastic scattering

    Directory of Open Access Journals (Sweden)

    Rand E. T.

    2014-03-01

    Full Text Available A nuclear structure campaign has been initiated to investigate the isotopes of mercury near A = 199. Currently 199Hg provides the most stringent limit on an atomic electric dipole moment (EDM. The observation of a permanent EDM would represent a clear signal of CP violation from new physics beyond the Standard Model. Theoretical calculations for 199Hg are very difficult and give varied predictions for the excited-state spectrum. Understanding the E2 and E3 strengths in the neighbouring even-even isotopes of mercury will make it possible to develop a nuclear structure model for the Schiff strength based on these matrix elements, and thereby constrain present model predictions of the contribution of octupole collectivity to the Schiff moment of the nucleus.

  13. Isotopic Composition of Gaseous Elemental Mercury (Hg0) at Various Sites in Japan

    Science.gov (United States)

    Yamakawa, A.; Moriya, K.; Yoshinaga, J.

    2015-12-01

    Mercury (Hg) is a toxic heavy metal, which exists in various chemical forms in the environmental system. In the atmosphere, Hg exists in three forms (Hg0(g), Hg+2(g), and Hg(p)). Hg0(g) is the dominant species of atmospheric Hg, accounting for >95% of the total Hg in the atmosphere. Because Hg0(g) is highly volatile and has limited solubility in water, it cannot be easily removed by wet or dry deposition processes. Therefore, the residence time of Hg0(g) in the atmosphere is relatively long (1 to 2 years), allowing long-range transport from mercury emission source(s). Conversely, Hg+2(g) and Hg(p) are effectively removed from the atmosphere through wet and dry depositions. The determination of mercury source attribution using quantitative data is challenging because Hg0(g) may be deposited on an area upon oxidation to Hg+2(g) and associated with aerosols and particulates to form Hg(p) while the global cycling of Hg0(g). Over the last decade, the development of analytical methods of highly precise Hg isotopic measurements demonstrated mass-dependent fractionation (MDF) and mass-independent fractionation (MIF) of Hg isotopes in environmental samples. For instance, MDF of Hg isotopes is thought to occur during various natural and industrial Hg transformations. MIF of Hg isotopes is observed during abiotic reduction, photochemical and non-photochemical, and physical and chemical processes. Such processes lead to differences in the Hg isotopic composition of different emission sources, both natural and anthropogenic, and atmospheric processes (i.e., transportation, oxidation/reduction, deposition, and reemission). Therefore, Hg isotopic compositions could be used to trace the sources and processes of atmospheric Hg. For securing the reliability and accuracy of atmospheric Hg isotope data, the methods of collection, pretreatment, and isotopic measurement for Hg0(g) were developed to obtain high recovery yield of samples with no Hg isotopic fractionation during each

  14. First principle study of the interaction of elemental Hg with small neutral, anionic and cationic Pd ( = 1-6) clusters

    Indian Academy of Sciences (India)

    Shamoon Ahmad Siddiqui; Nadir Bouarissa

    2013-11-01

    Density functional theory (DFT)-based calculations have been performed so as to study the interaction of elemental mercury (Hg) with small neutral, cationic and anionic palladium clusters (Pd, = 1-6). Results of these calculations clearly indicate that frontier molecular orbital (FMO) theory is a useful method to predict the selectivity of Hg adsorption. Binding energies of Hg on cationic Pd clusters are generally found to be greater than those on neutral and anionic clusters. Results of natural bond orbital (NBO) analysis show that the flow of electrons in the neutral and charged complexes is mainly due to s orbitals of Hg. NBO analysis also indicates that, in most of the cases, the binding energies of Hg with Pdn clusters are directly proportional to charge transfer, i.e., greater the charge transfer, higher is the binding energy.

  15. 合金元素对Mg-Hg-Ga阳极材料电化学行为的影响%Influence of Alloying Elements on Electrochemical Behavior of Mg-Hg-Ga Anodes

    Institute of Scientific and Technical Information of China (English)

    冯艳; 王日初; 彭超群

    2011-01-01

    用恒电流法,析氢法和交流阻抗法等方法测试了合金元素Hg和Ga对镁阳极电化学腐蚀行为的影响,并用扫描电镜和X射线衍射法分析了合金元素Hg和Ga对镁阳极的显微组织和相结构的影响。结果表明:铸态的Mg-4.8%Hg-8.8Ga合金晶界析出Mg5Ga2和Mg21Ga5Hg3相,铸态的Mg-8.8%Hg-8%Ga和Mg-7.2%Hg-8%Ga合金晶界析出Mg21Ga5Hg3相,铸态的Mg-7.2%Hg-2.6%Ga合金析出Mg3Hg和Mg21Ga5Hg3相。各合金析氢速率从小到大依次为:Mg-7.2%Hg-2.6%Ga合金,Mg-4.8%Hg-8%Ga合金,Mg-7.2%Hg-8%Ga合金和Mg-8.8%Hg-8%Ga合金。最小的析氢速率为1.75ml/(cm2.min)。各合金电化学活性从大到小依次为:Mg-8.8%Hg-8%Ga合金,Mg-7.2%Hg-8%Ga合金,Mg-4.8%Hg-8%Ga合金和Mg-7.2%Hg-2.6%Ga合金。在200 mA/cm2恒电流测试中最负的稳定电位-1.932 V出现在Mg-8.8%Hg-8%Ga合金中。%The effects of alloying elements Hg and Ga on the electrochemical corrosion behavior of Mg anodes were studied by galvanostatic tests,hydrogen evolution tests and electrochemical impedance spectra(EIS) measurements under different polarization conditions.Scanning electron microscopy(SEM) and X-ray diffractometry(XRD) were employed to detect the microstructure and phase relationship of the above alloys.Attention was paid to the combined effect of Hg and Ga on electrochemical properties and microstructures.The results show that Mg5Ga2 and Mg21Ga5Hg3 phases precipitated along the grain boundaries in cast Mg-4.8%Hg-8%Ga alloy.Mg21Ga5Hg3 phases precipitated in cast Mg-8.8%Hg-8%Ga and Mg-7.2%Hg-8%Ga alloys.Mg3Hg and Mg21Ga5Hg3 phases precipitated in cast Mg-7.2%Hg-2.6%Ga alloy.The sequential order of the hydrogen evolution corrosion rates from small to large is Mg-7.2%Hg-2.6%Ga alloy,Mg-4.8%Hg-8%Ga alloy,Mg-7.2%Hg-8%Ga alloy,and Mg-8.8%Hg-8%Ga alloy.The smallest hydrogen evolution corrosion rate is 1.75 ml/(cm2·min).The sequential order of the electrochemical activity from large to small is Mg-8.8%Hg-8

  16. Valence of elements in HgBa2Can-1CunO2n+2+d (n=1, 2, 3, 4)

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    Valence of elements in HgBa2Can-1CunO2n+2+d (n=1, 2, 3, 4) (both argon and oxygen annealed samples) were calculated. The result indicated for both argon and oxygen annealed samples, Hg had the lowest valence for the highest Tc sample. For fixed n, the valence of Cu in oxygen annealed samples was larger than that in argon annealed samples, indicating that oxygen annealed samples produce more carriers than argon annealed samples.

  17. Broadening and shift of the intercombination spectral line of the second group elements (Hg, Cd and Zn) perturbed by inert gases

    International Nuclear Information System (INIS)

    The Van der Waals and Lennard - Jones potential parameters for the ground and exited states of the second group elements (Hg, Cd and Zn) perturbed by inert gases (Xe, Kr, Ar, Ne and He) have been calculated using coulomb approximation. The basis of the Lindholm -Foley impact theory and the calculated potential parameters are used for calculating the collision broadening and shift coefficients β and δ for the intercombination lines 253.7, 326.1 and 307.6 nm of Hg, Cd and Zn atoms respectively when they are colliding with inert gas atoms . The calculating coefficients of β and δ are compared with their corresponding experimental values, taken from literatures

  18. A relativistic periodic DFT study on interaction of superheavy elements 112 (Cn) and 114 (Fl) and their homologs Hg and Pb, respectively, with a quartz surface.

    Science.gov (United States)

    Pershina, V

    2016-06-29

    Relativistic periodic calculations of adsorption energies of group-12 elements Hg and Cn and group-14 elements Pb and Fl on a hydroxylated (001) α-quartz surface at different adsorbate coverage have been performed using the ADF-BAND program. Results for the (4 × 4) supercell, being in good agreement with gas-phase chromatography experimental data for adsorption of Hg and Pb on quartz at zero coverage, indicate that Cn and Fl should not interact with the silicon oxide at room temperature. However, their moderately strong interaction with gold is expected. The reason for the non-interaction of Cn and Fl with SiO2 is strong relativistic effects on their valence electron shells. PMID:27315587

  19. Functional role of inorganic trace elements in angiogenesis part III: (Ti, Li, Ce, As, Hg, Va, Nb and Pb).

    Science.gov (United States)

    Saghiri, Mohammad Ali; Orangi, Jafar; Asatourian, Armen; Sorenson, Christine M; Sheibani, Nader

    2016-02-01

    Many essential elements exist in nature with significant influence on human health. Angiogenesis is vital in developmental, repair, and regenerative processes, and its aberrant regulation contributes to pathogenesis of many diseases including cancer. Thus, it is of great importance to explore the role of these elements in such a vital process. This is third in a series of reviews that serve as an overview of the role of inorganic elements in regulation of angiogenesis and vascular function. Here we will review the roles of titanium, lithium, cerium, arsenic, mercury, vanadium, niobium, and lead in these processes. The roles of other inorganic elements in angiogenesis were discussed in part I (N, Fe, Se, P, Au, and Ca) and part II (Cr, Si, Zn, Cu, and S) of these series. The methods of exposure, structure, mechanisms, and potential activities of these elements are briefly discussed. An electronic search was performed on the role of these elements in angiogenesis from January 2005 to April 2014. These elements can promote and/or inhibit angiogenesis through different mechanisms. The anti-angiogenic effect of titanium dioxide nanoparticles comes from the inhibition of angiogenic processes, and not from its toxicity. Lithium affects vasculogenesis but not angiogenesis. Nanoceria treatment inhibited tumor growth by inhibiting angiogenesis. Vanadium treatment inhibited cell proliferation and induced cytotoxic effects through interactions with DNA. The negative impact of mercury on endothelial cell migration and tube formation activities was dose and time dependent. Lead induced IL-8 production, which is known to promote tumor angiogenesis. Thus, understanding the impact of these elements on angiogenesis will help in development of new modalities to modulate angiogenesis under various conditions. PMID:26638864

  20. Assessment of micro, macro, toxic elements (Cd, Hg, Pb) and fatty acids profile in consumed fish commercially available in Cananeia and Cubatao, Sao Paulo State

    International Nuclear Information System (INIS)

    Aside from their nutritional importance, fish are considered one of the most important bio indicators in aquatic systems for the estimation of pollution levels by toxic metals. This is so, since fish can bio accumulate these elements and they occupy different trophic levels and present different sizes and age. The purpose of the present study was to contribute with important data for the knowledge of nutritional and toxic constituents in muscles of the most consumed fish species from two coastal regions, Cananeia and Cubatao. Cananeia fish species analyzed were: Micropogonias furnieri (Corvina), Macrodon ancylodon (Pescada), Centropomus undecimalis (Robalo peba) and Mugil platanus (Tainha). From Cubatao, Micropogonias furnieri (Corvina), Macrodon ancylodon (Pescada), Menticirrhus americanus (Perna de moca), Sardella braziliensis (Sardinha) and Mugil liza (Tainha). For this study, analytical methodologies were developed and validated, regarding precision and accuracy, by means of certified reference materials. Micronutrients (Ca, Fe, K, Na, Se and Zn) and some trace elements (As, Br, Co, Cr, Rb) in fish muscle were determined by means of neutron activation analysis (NAA). Cold Vapor Atomic Absorption Spectrometry (CV AAS) was used for total Hg determination and Electrothermal Atomic Absorption Spectrometry (ET AAS) for Cd and Pb determinations. Proximate composition determinations according to AOAC methodologies and fatty acids profiles by gas chromatography were done in these muscle fish samples. Regarding fatty acids profile from the ω-6 family, Tainha species pool presented the highest values (8.9%) and Pescada species pool the lowest ones (4.4%) for Cananeia species. Fatty acids from the ω-3 family, Sardinha pool species presented the highest values (31.8%) for all species analyzed. Regarding micronutrients content great concentration variations between individual of the same species and between different species were observed. Discriminate analysis was used

  1. Confirmation of the Decay of 283112 and First Indication for Hg-like Behavior of Element 112

    International Nuclear Information System (INIS)

    Two gas phase adsorption chemistry experiments aimed at the chemical characterization of element 112 using its isotope 283112 have been performed at the Flerov Laboratory for Nuclear Reactions (FLNR) Dubna, Russia. The applied Insitu-Volatilization and On-line Detection (IVO) technique is a thermochromatographic system combining the determination of the deposition temperature of volatile elements on a surface along a temperature gradient with an efficient detection of the deposited species by event-by-event alpha and SF-fragment spectroscopy. Two possibilities to produce the isotope 283112 were used: 1.) the direct production reaction 238U(48Ca,3n)283112; 2.) the reaction 242Pu(48Ca,3n), where the primary product 287114, decays via alpha emission to 283112 with a half-life of 0.5 s. The chemistry experiments were aimed at a chemical identification of 283112 and an independent confirmation of its decay properties. In the direct reaction no decays related to 283112 were observed. However, two decay chains unambiguously attributed to the decay of 283112 were observed using the second production path. Previously reported observation of 283112 and 279Ds and their decay properties were confirmed. From its thermochromatorgaphic deposition first thermochemical data were deduced for element 112, unveiling it as a typical group 12 element

  2. Metallic elements (Ca, Hg, Fe, K, Mg, Mn, Na, Zn) in the fruiting bodies of Boletus badius.

    Science.gov (United States)

    Kojta, Anna K; Falandysz, Jerzy

    2016-06-01

    The aim of this study was to investigate and compare the levels of eight metallic elements in the fruiting bodies of Bay Bolete (Boletus badius; current name Imleria badia) collected from ten sites in Poland to understand better the value of this popular mushroom as an organic food. Bay Bolete fruiting bodies were collected from the forest area near the towns and villages of Kętrzyn, Poniatowa, Bydgoszcz, Pelplin, Włocławek, Żuromin, Chełmno, Ełk and Wilków communities, as well as in the Augustów Primeval Forest. Elements such as Ca, Fe, K, Mg, Mn, Na and Zn were analyzed by inductively coupled plasma atomic emission spectroscopy (ICP-OES), and mercury by cold vapor atomic absorption spectrometry (CV-AAS). This made it possible to assess the nutritional value of the mushroom, as well as possible toxicological risks associated with its consumption. The results were subjected to statistical analysis (Kruskal-Wallis test, cluster analysis, principal component analysis). PMID:26830580

  3. Determination of As, Cd, Cr, and Hg in SRM 2584 (Trace Elements in Indoor Dust) by high-resolution inductively coupled plasma mass spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Yu, L.L.; Vocke, R.D.; Murphy, K.E.; Beck, C.M. II [Analytical Chemistry Div., National Institute of Standards and Technology, Gaithersburg, MD (United States)

    2001-08-01

    Standard reference material (SRM) 2584 (Trace Elements in Indoor Dust) was developed as a reference standard for evaluating field methods and for validating laboratory and reference methods for the assessment of lead contamination and exposure. In addition to lead, the toxic trace elements As, Cd, Cr, and Hg, at approximately 17, 10, 140, and 5 {mu}g g{sup -1}, respectively, have been certified in the SRM. These four analytes were successfully determined by use of high-resolution inductively coupled plasma mass spectrometry (HR-ICP-MS). Isobaric interferences at masses of As and Cr were resolved by using the high resolution mode (nominal 8000) and the medium resolution mode (nominal 3000), respectively, of the instrument.The effects of a significant drift in analyte sensitivity in the course of measurement were rectified by use of internal standardization, single spike standard addition, and an optimized analysis sequence. The results were compared with those obtained by instrumental neutron activation analysis (INAA) and isotope dilution inductively coupled plasma mass spectrometry (ID-ICP-MS). The results for the quality control, SRM 2704 (Buffalo River Sediment), were in good agreement with the certified values, indicated by the uncertainty intervals of the measured values overlapping the certified intervals at 95% confidence level. (orig.)

  4. Determination of Hg and other elements in fish and plant samples from Amazonic region, by neutron activation analysis; Determinacao de Hg e outros elementos de interesse em amostras de peixes e plantas da regiao amazonica, por analise por ativacao com neutrons

    Energy Technology Data Exchange (ETDEWEB)

    Favaro, Debora I.T.; Vasconcellos, Marina B.A. [Instituto de Pesquisas Energeticas e Nucleares (IPEN), Sao Paulo, SP (Brazil). Supervisao de Radioquimica; Fostier, Anne Helene [Centro de Energia Nuclear na Agricultura (CENA), Piracicaba, SP (Brazil). Lab. de Quimica Analitica

    1996-07-01

    In the present work the region of Serra do Navio, Amapa State, was chosen to asses the Hg contamination due to gold mining activities. As part of monitoring of this region, fishes and plants were collected and analysed by instrumental neutron activation (INAA). Through this method it was possible to determine the concentration of the elements: As, Ca, Cr, Co, Fe, Hg, Rb, Sb, Se and Zn in fishes and Ca, Co, Cr, Fe, Hg, La, Na, Rb, Sb, Sc, Se and Zn in plants. Mercury concentrations found in fishes ranged from 0.64 to 1.11 {mu}/g and from 0.83 to 0.15 {mu}g/g in plants. These results were compared with those obtained by the atomic absorption technique and they agreed well. The accuracy and precision of the INAA method were checked by means of analyses of reference materials. (author)

  5. Mass Independent Fractionation of Hg Isotopes Preserved in the Precambrian

    Science.gov (United States)

    Thibodeau, A. M.; Bergquist, B. A.; Kah, L. C.; Ono, S.; Ghosh, S.; Hazen, R. M.

    2013-12-01

    Mercury (Hg) is a photochemically active, redox-sensitive, chalcophilic metal with complex biogeochemistry that displays a wide range of mass-dependent (MDF) and mass-independent (MIF) stable isotopic fractionation. In the past decade, Hg isotopes have emerged as important tracers of both the sources and cycling of Hg in the modern environment. However, their utility as environmental proxies in ancient rocks remains largely unexplored. The potential of Hg isotopes to inform Precambrian environments derives from the observation that Hg isotopes with odd atomic mass numbers (199Hg and 201Hg) undergo large MIF by the magnetic isotope effect (MIE) and smaller MIF through the nuclear volume effect (NVE). Small MIF produced via NVE has been observed for numerous transformations and is characterized by MIF ratios (Δ199Hg/Δ201Hg) of about 1.6. Large Hg-MIF driven by MIE has been observed during photochemical transformations and is characterized by Δ199Hg/Δ201Hg ratios between 1 and 1.3. This MIF signal is sensitive to a range of environmental conditions, including the amount and type of solar radiation, the presence and type of complexing organic ligands, and the Hg/dissolved organic carbon (DOC) ratio. Thus, it is hoped that Hg-MIF signals may indirectly record changes in atmospheric composition or seawater chemistry if preserved in marine sedimentary records. Previous work has clearly demonstrated that Hg-MIF signals are preserved in Archean and Paleoproterozoic marine shales and massive sulfide deposits. Here, we present evidence that such signals are also preserved in marine shales of mid-Proterozoic age, including the ~1.3 Ga Sulky formation (Dismal Lakes Group, NW Arctic), the ~1.45 Ga Greyson Shale (Belt Basin, Montana), and the ~1.5 Ga Katalsy formation (Kypry Group, Eastern European Platform). We observe that the Greyson shale and shales within the Sulky formation yield negative Hg-MIF with Δ199Hg/Δ201Hg ratios close to 1 and that Kaltasy group sediments

  6. Se-Hg Dual-element Labeling Strategy for Selectively Recognizing Selenoprotein and Selenopeptide%硒-汞双元素标记策略识别硒蛋白/多肽

    Institute of Scientific and Technical Information of China (English)

    徐明; 杨利民; 王秋泉

    2015-01-01

    提出并发展了一种基于电感耦合等离子体质谱( ICP-MS)的双元素标签标记策略来选择性识别和检测硒蛋白/多肽,其中内源元素硒( Se)作为硒蛋白/多肽分子的识别元素,外源元素汞( Hg)作为硒蛋白/多肽和含硒蛋白/多肽分子的区分元素。通过对硒代半胱氨酸(SeCys)和谷胱甘肽过氧化酶1(GPx1)两种模型分子的研究,外源邻羧基苯硫甲基汞( CH3 Hg-THI )动态解离的 CH3 Hg+能够选择性标记硒代半胱氨酸残基( SeCys)中硒醇基(-SeH),但不能标记含硒蛋白/多肽分子的硒代蛋氨酸残基( SeMet)中的—SeCH3,进而依据Se和Hg的ICP-MS信号识别和检测硒蛋白/多肽。本方法应用于富硒酵母水溶性提取液的分析,结果表明,提取液中的硒蛋白/多肽能够被有效识别和检测,验证了Se-Hg双元素标签标记策略的发展是ICP-MS识别和检测硒蛋白/多肽的一种可行且优越的途径。%An endogenous element-label plus exogenous element-tag strategy was proposed for inductively coupled plasma mass spectrometry ( ICP-MS) to screen and discriminate a family of ultratrace but biological important biomolecules. The feasibility of this novel idea has been demonstrated when setting seleno ( SeCys) and Se-containing ( SeMet) proteins ( peptides) as an example. Se-label naturally occurring in the biomole-cules acts an identifier for picking them up out of large amount of various coexisting proteins ( peptides) , and CH3 Hg-tag that can bind to SeCys but not SeMet fulfills the task of discriminating seleno and Se-containing ones based on the Se and Hg signals on ICP-MS. After confirmed using SeCys and GPx1, the Se-Hg dual-element labeling strategy together with ICP-MS was applied to screen and discriminate seleno and Se-contai-ning proteins ( peptides) in the water-soluble extracts of Se-enriched yeast, and seven selenoproteins ( pep-tides) were detected with both 202 Hg and 82 Se signals out of fifteen Se

  7. 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

  8. Microbial Oxidation of Hg(0) - Its Effect on Hg Stable Isotope Fractionation and Methylmercury Production

    Energy Technology Data Exchange (ETDEWEB)

    Yee, Nathan [Rutgers Univ., New Brunswick, NJ (United States); Barkay, Tamar [Rutgers Univ., New Brunswick, NJ (United States); Reinfelder, John [Rutgers Univ., New Brunswick, NJ (United States)

    2016-06-28

    Mercury (Hg) associated with mixed waste generated by nuclear weapons manufacturing has contaminated vast areas of the Oak Ridge Reservation (ORR). Neurotoxic methylmercury (MeHg) has been formed from the inorganic Hg wastes discharged into headwaters of East Fork Poplar Creek (EFPC). Thus, understanding the processes and mechanisms that lead to Hg methylation along the flow path of EFPC is critical to predicting the impacts of the contamination and the design of remedial action at the ORR. In part I of our project, we investigated Hg(0) oxidation and methylation by anaerobic bacteria. We discovered that the anaerobic bacterium Desulfovibrio desulfuricans ND132 can oxidize elemental mercury [Hg(0)]. When provided with dissolved elemental mercury, D. desulfuricans ND132 converts Hg(0) to Hg(II) and neurotoxic methylmercury [MeHg]. We also demonstrated that diverse species of subsurface bacteria oxidizes dissolved elemental mercury under anoxic conditions. The obligate anaerobic bacterium Geothrix fermentans H5, and the facultative anaerobic bacteria Shewanella oneidensis MR-1 and Cupriavidus metallidurans AE104 can oxidize Hg(0) to Hg(II) under anaerobic conditions. In part II of our project, we established anaerobic enrichment cultures and obtained new bacterial strains from the DOE Oak Ridge site. We isolated three new bacterial strains from subsurface sediments collected from Oak Ridge. These isolates are Bradyrhizobium sp. strain FRC01, Clostridium sp. strain FGH, and a novel Negativicutes strain RU4. Strain RU4 is a completely new genus and species of bacteria. We also demonstrated that syntrophic interactions between fermentative bacteria and sulfate-reducing bacteria in Oak Ridge saprolite mediate iron reduction via multiple mechanisms. Finally, we tested the impact of Hg on denitrification in nitrate reducing enrichment cultures derived from subsurface sediments from the Oak Ridge site, where nitrate is a major contaminant. We showed that there is an inverse

  9. A New Geochemical Classification of Elements

    Institute of Scientific and Technical Information of China (English)

    Qi Changmou; L. Lynn Chyi

    2001-01-01

    The geochemical classification proposed by Goldschmidt was based on meteoritic analysis and elemental partition in blast furnace. There are many surprises when applied to the discussion of natural occurrences. A modified classification of elements based on basic chemical properties and their occurrences. A modified classification of elements based on basic chemical properties and their occurrences in nature is, therefore, proposed for students learning geochemistry and geologists working in the field. Elements are classified into six groups including lithophile, oxyphile, siderophile, chalcophile, biophile, and atmophile elements. Five terms are taken from Goldshcmidt's original classification. Oxyphile is a new term.

  10. 4482 Element Multispectral Hybrid PV/PC HgCdTe IRFPA for High Resolution Coverage of 3.7 - 15.4 Micrometers for the AIRS Instrument

    Science.gov (United States)

    Rutter, James; Libonate, Scott; Denley, Brian; Gurnee, Mark N.; Robillard, Gene

    1996-01-01

    The Atmospheric Infrared Sounder (AIRS) is a key facility instrument in the NASA Earth Observing System (EOS) program, being implemented to obtain comprehensive long-term measurements of earth processes affecting global change. The instrument performs passive IR remote sensing using a high resolution grating spectrometer with a wide spectral coverage (3.7 - 15.4 m) directing radiation onto a hybrid HgCdTe IRFPA operating at 58K in a vacuum package cooled to 155K. The hybrid HgCdTe FPA consists of twelve modules, 10 with multiplexed photovoltaic detectors and two with individually leaded out photoconductive detectors. The complex FPA has a large optical footprint, 53 mm x 66 mm, and receives energy dispersed from the grating through a precision filter assembly containing 17 narrow band filters. The backside illuminated PV detector arrays are fabricated from P-on-n double layer LPE grown heterojunction detectors in a bilinear format of 50 m x 100 m detectors, with from 232 to 420 detectors per module. For the MWIR bands four PV modules cover the 3.7 m to 8.22 m region. Low detector capacitance and low noise preamplifiers in the ROIC are key to achieving high sensitivities in these bands. Uniform quantum efficiencies and detectivities exceeding 3E13 cm-rtHz/W have been achieved. The LWIR region is covered by six PV modules spanning 8.8 m to 13.75 m. High detector resistance and very low ROIC preamplifier input noise are key to achieving high sensitivity. A detectivity exceeding 2E11 cm-rtHz/W has been achieved at the longest wavelength. Two additional PC modules cover the longest spectral bands out to 15.4 m. This high performance multispectral focal plane has been built and integrated with the dewar assembly, and is currently being integrated with the complete AIRS sensor.

  11. Highly Siderophile and Chalcophile Elements in Lunar Impact Rocks: Constraints on the Composition of Late Accreted Material

    Science.gov (United States)

    Gleißner, P.; Becker, H.

    2016-08-01

    HSE, Te, Se and S composition of ancient lunar impactites reveal the late accretion of chondrite-like material along with differentiated core metal. HSE patterns are consistent with parent body P/S ratios higher than most magmatic iron meteorites.

  12. Assessment of micro, macro, toxic elements (Cd, Hg, Pb) and fatty acids profile in consumed fish commercially available in Cananeia and Cubatao, Sao Paulo State; Avaliacao de micro e macroelementos, elementos toxicos (Cd, Hg e Pb) e acidos graxos, em peixes disponiveis comercialmente para consumo em Cananeia e Cubatao, Estado de Sao Paulo

    Energy Technology Data Exchange (ETDEWEB)

    Curcho, Michel Rodrigues da Silva Morales

    2009-07-01

    Aside from their nutritional importance, fish are considered one of the most important bio indicators in aquatic systems for the estimation of pollution levels by toxic metals. This is so, since fish can bio accumulate these elements and they occupy different trophic levels and present different sizes and age. The purpose of the present study was to contribute with important data for the knowledge of nutritional and toxic constituents in muscles of the most consumed fish species from two coastal regions, Cananeia and Cubatao. Cananeia fish species analyzed were: Micropogonias furnieri (Corvina), Macrodon ancylodon (Pescada), Centropomus undecimalis (Robalo peba) and Mugil platanus (Tainha). From Cubatao, Micropogonias furnieri (Corvina), Macrodon ancylodon (Pescada), Menticirrhus americanus (Perna de moca), Sardella braziliensis (Sardinha) and Mugil liza (Tainha). For this study, analytical methodologies were developed and validated, regarding precision and accuracy, by means of certified reference materials. Micronutrients (Ca, Fe, K, Na, Se and Zn) and some trace elements (As, Br, Co, Cr, Rb) in fish muscle were determined by means of neutron activation analysis (NAA). Cold Vapor Atomic Absorption Spectrometry (CV AAS) was used for total Hg determination and Electrothermal Atomic Absorption Spectrometry (ET AAS) for Cd and Pb determinations. Proximate composition determinations according to AOAC methodologies and fatty acids profiles by gas chromatography were done in these muscle fish samples. Regarding fatty acids profile from the {omega}-6 family, Tainha species pool presented the highest values (8.9%) and Pescada species pool the lowest ones (4.4%) for Cananeia species. Fatty acids from the {omega}-3 family, Sardinha pool species presented the highest values (31.8%) for all species analyzed. Regarding micronutrients content great concentration variations between individual of the same species and between different species were observed. Discriminate analysis

  13. 碳汞比对燃煤烟气中Hg脱除影响的实验研究%THE EXPERIMENTAL STUDY ON THE INFLUENCE OF C/Hg RATIO ON REMOVAL OF ELEMENTAL MERCURY IN SIMULATED FLUE GAS

    Institute of Scientific and Technical Information of China (English)

    丁建东; 陈博; 刁永发; 沈恒根; 石健

    2012-01-01

    Using combined system of adsorption reactor and bag filter, the effects of the removal of elemental mercury by activated carbon injection in simulated flue gas were studied. Experiments showed that the adsorption of elemental mercury in the adsorption reactor played a major role and the removal of mercury increased with the increase of C/Hg ratio. The C/Hg ratio had little effect to the removal of mercury of the bag filter. The total removal of mercury by the system was 39.9% , 42. 5% , 47.3% under the C/Hg ratio at 4 000,6 000 and 8 000 respectively. Meanwhile, the characteristic of the removal of mercury by the dust layer on the filter was estimated. The results showed that the removal of mercury by the dust layer was 3.65% , 3.20% and 3.66%. under the C/Hg ratio at 4 000,6 000,8 000 respectively, at 0.98 m/min in the surface filtration velocity.%利用吸附反应器和袋式除尘器联合脱汞系统,研究了活性炭喷射对模拟烟气中元素汞的脱除影响。实验表明,吸附反应器对元素汞的脱除起主要作用,并且脱汞效率随碳汞比的增加而提高;碳汞比的变化对除尘器的脱汞效率影响不大。在碳汞比为4000、6000、8000下,系统的脱汞效率分别为39.9%、42.5%、47.3%。实验同时探讨了除尘器滤袋上粉尘层的存在对脱汞效率的影响,结果表明:在表面过滤速度为0.98m/min的实验条件下,在碳汞比为4000、6000、8000下,粉尘层的脱汞效率分别为:3.65%、3.20%、3.66%。

  14. A Theoretical Study of the Oxidation of Hg0 to HgBr2 in the Troposphere

    DEFF Research Database (Denmark)

    Goodsite, M. E.; Plane, J. M C; Skov, H.

    2004-01-01

    The oxidation of elemental mercury (Hg0) to the divalent gaseous mercury dibromide (HgBr2) has been proposed to account for the removal of Hg0 during depletion events in the springtime Arctic. The mechanism of this process is explored in this paper by theoretical calculations of the relevant rate...

  15. Distribution and air-sea exchange of mercury (Hg) in the Yellow Sea

    OpenAIRE

    Z. J. Ci; X. S. Zhang; Wang, Z. W.; Niu, Z. C.; Diao, X. Y.; Wang, S. W.

    2011-01-01

    The Yellow Sea, surrounded by East China and the Korea Peninsula, is a potentially important receptor for anthropogenic mercury (Hg) emissions from East Asia. However, there is little documentation about the distribution and cycle of Hg in this marine system. During the cruise covering the Yellow Sea in July 2010, gaseous elemental mercury (GEM or Hg(0)) in the atmosphere, total Hg (THg), reactive Hg (RHg) and dissolved gaseous mercury (DGM, largely Hg(0)) in the waters were measured ...

  16. Results Of Hg Speciation Testing On DWPF SMECT-1, SMECT-3, And SMECT-5 Samples

    Energy Technology Data Exchange (ETDEWEB)

    Bannochie, C. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

    2016-01-07

    The Savannah River National Laboratory (SRNL) was tasked with preparing and shipping samples for Hg speciation by Eurofins Frontier Global Sciences, Inc. in Seattle, WA on behalf of the Savannah River Remediation (SRR) Mercury Task Team. The thirteenth shipment of samples was designated to include Defense Waste Processing Facility (DWPF) Slurry Mix Evaporator Condensate Tank (SMECT) from Sludge Receipt and Adjustment Tank (SRAT) Batch 736 and 738 samples. Triplicate samples of each material were prepared for this shipment. Each replicate was analyzed for seven Hg species: total Hg, total soluble (dissolved) Hg, elemental Hg [Hg(0)], ionic (inorganic) Hg [Hg(I) and Hg(II)], methyl Hg [CH3Hg-X, where X is a counter anion], ethyl Hg [CH3CH2-Hg-X, where X is a counter anion], and dimethyl Hg [(CH3)2Hg]. The difference between the total Hg and total soluble Hg measurements gives the particulate Hg concentration, i.e. Hg adsorbed to the surface of particulate matter in the sample but without resolution of the specific adsorbed species. The average concentrations of Hg species in the aqueous samples derived from Eurofins reported data corrected for dilutions performed by SRNL are tabulated.

  17. Magnetic fields of HgMn stars

    DEFF Research Database (Denmark)

    Hubrig, S.; Gonzalez, J. F.; Ilyin, I.;

    2012-01-01

    Context. The frequent presence of weak magnetic fields on the surface of spotted late-B stars with HgMn peculiarity in binary systems has been controversial during the two last decades. Recent studies of magnetic fields in these stars using the least-squares deconvolution (LSD) technique have...... by applying the moment technique on spectral lines of inhomogeneously distributed elements separately. Furthermore, we present new determinations of the mean longitudinal magnetic field for the HgMn star HD 65949 and the hotter analog of HgMn stars, the PGa star HD 19400, using FORS 2 installed at the VLT. We...... also give new measurements of the eclipsing system ARAur with a primary star of HgMn peculiarity, which were obtained with the SOFIN spectropolarimeter installed at the Nordic Optical Telescope. Methods. We downloaded from the European Southern Observatory (ESO) archive the publically available HARPS...

  18. Microbial Oxidation of Hg(0) - Its Effect on Hg Stable Isotope Fractionation and Methylmercury Production

    Energy Technology Data Exchange (ETDEWEB)

    Yee, Nathan [Rutgers Univ., New Brunswick, NJ (United States); Barkay, Tamar [Rutgers Univ., New Brunswick, NJ (United States); Reinfelder, John [Rutgers Univ., New Brunswick, NJ (United States)

    2016-06-28

    Mercury (Hg) associated with mixed waste generated by nuclear weapons manufacturing has contaminated vast areas of the Oak Ridge Reservation (ORR). Neurotoxic methylmercury (MeHg) has been formed from the inorganic Hg wastes discharged into headwaters of East Fork Poplar Creek (EFPC). Thus, understanding the processes and mechanisms that lead to Hg methylation along the flow path of EFPC is critical to predicting the impacts of the contamination and the design of remedial action at the ORR. In part I of our project, we investigated Hg(0) oxidation and methylation by anaerobic bacteria. We discovered that the anaerobic bacterium Desulfovibrio desulfuricans ND132 can oxidize elemental mercury [Hg(0)]. When provided with dissolved elemental mercury, D. desulfuricans ND132 converts Hg(0) to Hg(II) and neurotoxic methylmercury [MeHg]. We also demonstrated that diverse species of subsurface bacteria oxidizes dissolved elemental mercury under anoxic conditions. The obligate anaerobic bacterium Geothrix fermentans H5, and the facultative anaerobic bacteria Shewanella oneidensis MR-1 and Cupriavidus metallidurans AE104 can oxidize Hg(0) to Hg(II) under anaerobic conditions. In part II of our project, we established anaerobic enrichment cultures and obtained new bacterial strains from the DOE Oak Ridge site. We isolated three new bacterial strains from subsurface sediments collected from Oak Ridge. These isolates are Bradyrhizobium sp. strain FRC01, Clostridium sp. strain FGH, and a novel Negativicutes strain RU4. Strain RU4 is a completely new genus and species of bacteria. We also demonstrated that syntrophic interactions between fermentative bacteria and sulfate-reducing bacteria in Oak Ridge saprolite mediate iron reduction via multiple mechanisms. Finally, we tested the impact of Hg on denitrification in nitrate reducing enrichment cultures derived from subsurface sediments from the Oak Ridge site, where nitrate is a major contaminant. We showed that there is an inverse

  19. Further Studies, About New Elements Production, by Electrolysis of Cathodic Pd Thin–Long Wires, in Alcohol-Water Solutions (H, D) and Th-Hg Salts. New Procedures to Produce Pd Nano-Structures

    CERN Document Server

    Celani, F; Righi, E; Trenta, G; Catena, C; D’Agostaro, G; Quercia, P; Andreassi, V; Marini, P; Di Stefano, V; Nakamura, M; Mancini, A; Sona, P G; Fontana, F; Gamberale, L; Garbelli, D; Celia, E; Falcioni, F; Marchesini, M; Novaro, E; Mastromatteo, U

    2005-01-01

    Abstract They were continued, at National Institute of Nuclear Physics, Frascati National Laboratories-Italy, the systematic studies about detection of new elements, some even with isotopic composition different from natural one, after prolonged electrolysis of Pd wires. The electrolytic solution adopted is the, unusual, used from our experimental group since 1999. In short, it was a mixture of both heavy ethyl alcohol (C2H5OD at 90-95%) and water (D2O, at 10-5%), with Th salts at micromolar concentration and Hg at even lower concentration (both of spectroscopic purity). The liquid solutions, before use, were carefully vacuum distilled (and on line 100nm filtered) at low temperatures (30-40°C) and analysed by ICP-MS. The pH was kept quite mild (acidic at about 3-4). The cathode is Pd (99.9% purity) in the shape of long (60cm) and thin wires (diameter only 0.05mm). Before use, it is carefully cleaned and oxidised by Joule heating in air following a (complex) procedure from us continuously improved (since 1995...

  20. Hg0 absorption in potassium persulfate solution

    Institute of Scientific and Technical Information of China (English)

    YE Qun-feng; WANG Cheng-yun; WANG Da-hui; SUN Guan; XU Xin-hua

    2006-01-01

    The aqueous phase oxidation of gaseous elemental mercury (Hg0) by potassium persulfate (KPS) catalyzed by Ag+was investigated using a glass bubble column reactor. Concentration of gaseous mercury and potassium persulfate were measured by cold vapor atom absorption (CVAA) and ion chromatograph (IC), respectively. The effects of pH value, concentration of potassium persulfate and silver nitrate (SN), temperature, Hg0 concentration in the reactor inlet and tertiary butanol (TBA), free radical scavenger, on the removal efficiency of Hg0 were studied. The results showed that the removal efficiency of Hg0 increased with increasing concentration of potassium persulfate and silver nitrate, while temperature and TBA were negatively effective. Furthermore, the removal efficiency of Hg0 was much better in neutral solution than in both acidic and alkaline solution. But the influence of pH was almost eliminated by adding AgNO3. High Hg0 concentration has positive effect. The possible reaction mechanism of gaseous mercury was also discussed.

  1. Observation of intergrowth structures of Hg-1212, Hg-1223 and Hg-1234 phases in a nominal Hg-1223 ceramic superconductor

    International Nuclear Information System (INIS)

    Intergrowth structures of the Hg-1223 superconductor containing other Hg superconducting phases such as Hg-1212 and Hg-1234 were observed under a transmission electron microscope. The X-ray diffraction pattern, the resistance-temperature relationship and the a.c. magnetic susceptibility-temperature relationships indicate that the sample contains mainly Hg-1223 phase. However, scanning electron microscope and energy dispersive X-ray analysis show that the sample contains intergrowth structures. In our previous joint work, two fundamental intergrowth structures were reported. Here we report two more intergrowth structures, namely Hg-1223/(Hg-1212, Hg-1223, Hg-1234) and Hg-1223/(Hg-1223, Hg-1234). Calculation of the ratio of strain energy density Ut and the Young modulus E001 along the (001) direction of the unit cell of the Hg sample shows that the value of Ut/E001 for the first region is 1.54*10-4 and for the second is 1.56*10-3. The reason for the formation of the ill-defined mismatch region in the second intergrowth structure may be due to the relatively large strain field in the conjunction boundary of the structure. (author)

  2. Anaerobic oxidation of Hg(0) and methylmercury formation by Desulfovibrio desulfuricans ND132

    Science.gov (United States)

    Colombo, Matthew J.; Ha, Juyoung; Reinfelder, John R.; Barkay, Tamar; Yee, Nathan

    2013-07-01

    The transformation of inorganic mercury (Hg) to methylmercury (MeHg) plays a key role in determining the amount of Hg that is bioaccumulated in aquatic food chains. An accurate knowledge of Hg methylation mechanisms is required to predict the conditions that promote MeHg production in aquatic environments. In this study, we conducted experiments to examine the oxidation and methylation of dissolved elemental mercury [Hg(0)] by the anaerobic bacterium Desulfovibrio desulfuricans ND132. Anoxic cultures of D. desulfuricans ND132 were exposed to Hg(0) in the dark, and samples were collected and analyzed for the loss of Hg(0), formation of non-purgeable Hg, and formation of MeHg over time. We found that D. desulfuricans ND132 rapidly transformed dissolved gaseous mercury into non-purgeable Hg, with bacterial cultures producing approximately 40 μg/L of non-purgeable Hg within 30 min, and as much as 800 μg/L of non-purgeable Hg after 36 h. Derivatization of the non-purgeable Hg in the cell suspensions to diethylmercury and analysis of Hg(0)-reacted D. desulfuricans ND132 cells using X-ray absorption near edge structure (XANES) spectroscopy demonstrated that cell-associated Hg was dominantly in the oxidized Hg(II) form. Spectral comparisons and linear combination fitting of the XANES spectra indicated that the oxidized Hg(II) was covalently bonded to cellular thiol functional groups. MeHg analyses revealed that D. desulfuricans ND132 produced up to 118 μg/L of methylmercury after 36 h of incubation. We found that a significant fraction of the methylated Hg was exported out of the cell and released into the culture medium. The results of this work demonstrate a previously unrecognized pathway in the mercury cycle, whereby anaerobic bacteria produce MeHg when provided with dissolved Hg(0) as their sole Hg source.

  3. The Vein-type Zn-(Pb, Cu, As, Hg mineralization at Fedj Hassène orefield, North-Western Tunisia: Mineralogy, Trace Elements, Sulfur Isotopes and Fluid Inclusions

    Directory of Open Access Journals (Sweden)

    Bejaoui, J.

    2011-06-01

    Full Text Available The Fedj Hassène 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 subparallel 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 Hassène, 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/cm3 and 1.11 g/cm3 and pressure close to 200 bars. Microthermometric data in fluid inclusion hosted by gangue mineral presented by calcite show an average temperature of formation around 194°C. These inclusions homogenized to the liquid phase between 156°C and 210°C and salinities values ranging from 22 to 28 wt% NaCl and an average around 23% wt NaCl. The δ34S (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 ?34S values. Mineralogical, geochemical of trace elements, fluid inclusions and sulfur isotopes studies allow to include the vein-type ore field of Fedj Hassène in the polymetallic (Pb-Zn-As-Hg vein mineralization of the nappe zone in northern Tunisia and north eastern Algeria

  4. Magnetic fields of HgMn stars

    CERN Document Server

    Hubrig, S; Ilyin, I; Korhonen, H; Schoeller, M; Savanov, I; Arlt, R; Castelli, F; Curto, G Lo; Briquet, M; Dall, T H

    2012-01-01

    The frequent presence of weak magnetic fields on the surface of spotted late-B stars with HgMn peculiarity in binary systems has been controversial during the two last decades. We re-analyse available spectropolarimetric material by applying the moment technique on spectral lines of inhomogeneously distributed elements separately. Furthermore, we present new determinations of the mean longitudinal magnetic field for the HgMn star HD65949 and the hotter analog of HgMn stars, the PGa star HD19400, using FORS2 installed at the VLT. We also give new measurements of the eclipsing system AR Aur with a primary star of HgMn peculiarity which were obtained with the SOFIN spectropolarimeter installed at the Nordic Optical Telescope. We downloaded from the ESO archive the publically available HARPS spectra for eight HgMn stars and one normal and one superficially normal B-type star obtained in 2010. The application of the moment technique to the HARPS and SOFIN spectra allowed us to study the presence of the longitudina...

  5. 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

  6. Study on the application of magnesium oxide adsorptive compound to preconcentrate trace elements (As, Cu, Co, Cr, Hg, Mn, Sb and Zn) in high salt water and neutron activation analysis

    International Nuclear Information System (INIS)

    The project presents preconcentration neutron activation analysis techniques for determination of trace metals (As, Co, Cr Cu, Hg, Mn, Sb and Zn) in high salt water by adsorption of trace metals on magnesium oxide. Precipitate is collected on 0.45 μm membrane filters and irradiated in pneumatic rabit system and Lazy Susan facility at flux 5.1012 n/cm2.sec for As, Cu, Mn and 2.1012 n/cm2.sec for Hg, Sb, Cr, Co and Zn. The radioactivities of 76As, 60Co, 64Cu, 51Cr, 203Hg, 56Mn, 124Sb and 65Zn were measured. 76As, 60Co, 64Cu, 51Cr, 203Hg, 56Mn, 124Sb and 65Zn radio traces were used to establish optimum conditions and to evaluate the chemical yield. Detection limits of this method are 0.019, 0.006, 0.044, 0.058, 0.021, 0.027, 0.012 and 0.094 μg of As, Co, Cr, Cu, Hg, Mn, Sb and Zn respectively. (author)

  7. Hg-Mask Coronagraph

    Science.gov (United States)

    Bourget, P.; Veiga, C. H.; Vieira Martins, R.; Assus, P.; Colas, F.

    In order to optimize the occulting process of a Lyot coronagraph and to provide a high dynamic range imaging, a new kind of occulting disk has been developed at the National Observatory of Rio de Janeiro. A mercury (Hg) drop glued onto an optical window by molecular cohesion and compressed by a pellicle film is used as the occulting disk. The minimum of the superficial tension potential function provides an optical precision (lambda/100) of the toric free surface of the mercury. This process provides a size control for the adaptation to the seeing conditions and to the apparent diameter of a resolved object, and in the case of adaptive optics, to the Airy diameter fraction needed. The occultation is a three dimensional process near the focal plane on the toric free surface that provides an apodization of the occultation. The Hg-Mask coronagraph has been projected for astrometric observations of faint satellites near to Jovian planets and works since 2000 at the 1.6 m telescope of the Pico dos Dias Observatory (OPD - Brazil).

  8. Beta Decay of Neutron-Rich Nucleus 208Hg

    Institute of Scientific and Technical Information of China (English)

    张立; 森田浩介; 胡青元; 吉田敦; 赵进华; 郑继文; 李占奎; 越虎蒲; 工藤久昭; 矢野安重

    2003-01-01

    The β- decaying γ scheme of the neutron-rich nuclide 208Hg has been determined for the first time. The 208Hg was produced in multi-nucleon transfer reaction taking place in the bombardment of 18 O-beam on natural lead target, and the Hg-element products were separated with a gas-thermochromatography technique. The γ-ray single and γ-γ coincident spectra were measured. A partial 208Hg γ scheme was proposed. Twenty-six γ rays were assigned to follow theβ- decay of 208Hg. At the same time, a new level structure of the daughter nucleus 208Tl was constructed, in which three new levels at 1.728 MeV, 1.652 MeV, and 1.362 MeV were affirmed. The experimental 208Tl level structure was compared with a shell-model calculation.

  9. Natural Hg isotopic composition of different Hg compounds in mammal tissues as a proxy for in vivo breakdown of toxic methylmercury.

    Science.gov (United States)

    Perrot, Vincent; Masbou, Jeremy; Pastukhov, Mikhail V; Epov, Vladimir N; Point, David; Bérail, Sylvain; Becker, Paul R; Sonke, Jeroen E; Amouroux, David

    2016-02-01

    In the last decade, specific attention has been paid to total mercury (HgT) stable isotopic composition, especially in natural samples such as aquatic organisms, due to its potential to track the cycle of this toxic element in the environment. Here, we investigated Hg Compound Specific stable Isotopic Composition (CSIC) of natural inorganic Hg (iHg) and methylmercury (MMHg) in various tissues of aquatic mammals (Beluga whale from the Arctic marine environment and seals from the freshwater lake Baikal, Russia). In seals' organs the variation in mass dependent fractionation (MDF, δ(202)Hg) for total Hg was significantly correlated to the respective fraction of iHg and MMHg compounds, with MMHg being enriched by ∼ 3‰ in heavier isotopes relative to iHg. On the other hand, we observe insignificant variation in Hg mass independent isotope fractionation (MIF, Δ(199)Hg) among iHg and MMHg in all organs for the same mammal species and MMHg in prey items. MIF signatures suggest that both MMHg and iHg in aquatic mammals have the same origin (i.e., MMHg from food), and are representative of Hg photochemistry in the water column of the mammal ecosystem. MDF signatures of Hg compounds indicate that MMHg is demethylated in vivo before being stored in the muscle, and the iHg formed is stored in the liver, and to a lesser extent in the kidney, before excretion. Thus, Hg CSIC analysis in mammals can be a powerful tool for tracing the metabolic response to Hg exposure.

  10. Natural Hg isotopic composition of different Hg compounds in mammal tissues as a proxy for in vivo breakdown of toxic methylmercury.

    Science.gov (United States)

    Perrot, Vincent; Masbou, Jeremy; Pastukhov, Mikhail V; Epov, Vladimir N; Point, David; Bérail, Sylvain; Becker, Paul R; Sonke, Jeroen E; Amouroux, David

    2016-02-01

    In the last decade, specific attention has been paid to total mercury (HgT) stable isotopic composition, especially in natural samples such as aquatic organisms, due to its potential to track the cycle of this toxic element in the environment. Here, we investigated Hg Compound Specific stable Isotopic Composition (CSIC) of natural inorganic Hg (iHg) and methylmercury (MMHg) in various tissues of aquatic mammals (Beluga whale from the Arctic marine environment and seals from the freshwater lake Baikal, Russia). In seals' organs the variation in mass dependent fractionation (MDF, δ(202)Hg) for total Hg was significantly correlated to the respective fraction of iHg and MMHg compounds, with MMHg being enriched by ∼ 3‰ in heavier isotopes relative to iHg. On the other hand, we observe insignificant variation in Hg mass independent isotope fractionation (MIF, Δ(199)Hg) among iHg and MMHg in all organs for the same mammal species and MMHg in prey items. MIF signatures suggest that both MMHg and iHg in aquatic mammals have the same origin (i.e., MMHg from food), and are representative of Hg photochemistry in the water column of the mammal ecosystem. MDF signatures of Hg compounds indicate that MMHg is demethylated in vivo before being stored in the muscle, and the iHg formed is stored in the liver, and to a lesser extent in the kidney, before excretion. Thus, Hg CSIC analysis in mammals can be a powerful tool for tracing the metabolic response to Hg exposure. PMID:26680232

  11. HCN Producing Bacteria Enable Sensing Of Non-Bioavailable Hg Species by the Whole Cell Biosensor

    Science.gov (United States)

    Horvat, M.; Rijavec, T.; Koron, N.; Lapanje, A.

    2015-12-01

    Bacteria play an important role in Hg transformation reactions. The production of cyanide (HCN) and other secondary metabolites seems to be key elements involved in these transformations. Current hypotheses link the role of HCN production to growth inhibition of nonHCN producing competitor organisms (role of an antimicrobial agent). Our past investigations showed that HCN production did not correlate with antimicrobial activity and since pK value of HCN is very high (pK = 9,21), it can be expected that most of the produced HCN is removed from the microenvironment. This way, the expected inhibitory concentrations can hardly be reached. Accordingly, we proposed a new concept, where the ability of complexation of transient metals by HCN served as a regulation process for the accessibility of micro-elements. In our study, we focused on the presence of HCN producing bacteria and carried it out in the Hg contaminated environment connected to the Idrija Mercury Mine, Slovenia. We characterised the isolates according to the presence of Hg resistance (HgR), level of HCN production and genetic similarities. In laboratory setups, using our merR whole cell based biosensor, we determined the transformation of low bioavailable Hg0 and HgS forms into bioavailable Hg by these HCN producing bacteria. We observed that HgR strains producing HCN had the highest impact on increased Hg bioavailability. In the proposed ecological strategy HgR HCN producing bacteria increase their competitive edge over non-HgR competitors through the increase of Hg toxicity. Due to their activity, Hg is made available to other organisms as well and thus enters into the ecosystem. Finally, using some of the characteristics of bacteria (e.g. Hg resistance genetic elements), we developed a fully automated sensing approach, combining biosensorics and mechatronics, to measure the bioavailability of Hg in situ.

  12. Chalcophile element (Ni, Cu, PGE, and Au) variations in the Tamarack magmatic sulfide deposit in the Midcontinent Rift System: implications for dynamic ore-forming processes

    Science.gov (United States)

    Taranovic, Valentina; Ripley, Edward M.; Li, Chusi; Rossell, Dean

    2016-10-01

    The Tamarack magmatic sulfide deposit is hosted by the Tamarack Intrusive Complex (1105.6 ± 1.2 Ma) in the Midcontinent Rift System. The most important sulfide mineralization in the Complex occurs in the northern part, which consists of two separate intrusive units: an early funnel-shaped layered peridotite body containing relatively fine-grained olivine (referred to as the FGO Intrusion) at the top, and a late gabbro-troctolite-peridotite dike-like body containing relatively coarse-grained olivine (referred to as the CGO Intrusion) at the bottom. Disseminated, net-textured, and massive sulfides occur in the base of the FGO Intrusion as well as in the upper part of the CGO Intrusion. The widest part of the CGO Intrusion also hosts a large semi-massive (net-textured) sulfide ore body locally surrounded by disseminated sulfide mineralization. Small massive sulfide veins occur in the footwall of the FGO Intrusion and in the wall rocks of the CGO dike. The sulfide mineralization is predominantly composed of pyrrhotite, pentlandite, and chalcopyrite, plus minor magnetite. Pyrrhotite containing the highest Ni and Co contents occurs in the FGO disseminated sulfides and in the CGO semi-massive sulfide ores, respectively. The most important platinum-group minerals associated with the base metal sulfides are sperrylite (PtAs2), sudburyite (PdSb), and michenerite (PdBiTe). Nickel shows a strong positive correlation with S in all types of sulfide mineralization, and Cu shows a strong positive correlation with S in the disseminated sulfide mineralization. At a given S content, the concentrations of Pt, Pd, and Au in the CGO disseminated sulfides are significantly higher than those in the FGO disseminated sulfides. The semi-massive sulfide ores are characterized by significantly higher IPGE (Ir, Os, Ru, and Rh) concentrations than most of the massive sulfide ores. With few exceptions, all of the various textural types of sulfide mineralization collectively show a good positive correlation between Pt and Pd, and between individual IPGE. At a given Pt or Pd content, however, the semi-massive sulfide ores have higher IPGE contents than the disseminated sulfide samples. Modeling results show that the variations in PGE tenors (metals in recalculated 100 % sulfide) in the Tamarack magmatic sulfide deposit are mainly controlled by variable R factors (magma/sulfide-liquid mass ratios) during sulfide-liquid segregation and subsequent monosulfide solid solution (MSS) fractionation during cooling. The initial contents of Ir, Pt, and Pd in the parental magma, estimated from the metal tenors of the disseminated sulfides, are 0.2, 2, and 1.8 ppb, respectively, which are ˜1/5 of the values for the PGE-undepleted primitive basalts of the Midcontinent Rift System. The variations of PGE tenors in the semi-massive and massive sulfide ores can be explained by MSS fractional crystallization from sulfide liquids. Extreme variations in the PGE contents of the massive sulfides may also in part reflect metal mobility during post-crystallization hydrothermal processes. The higher PGE tenors for the disseminated sulfides in the CGO dike relative to those in the FGO Intrusion are consistent with formation in a dynamic conduit where the early sulfide liquids left in the conduit by the FGO magma were subsequently upgraded by the subsequent surge of the CGO magma. The relatively low PGE tenors for the semi-massive and massive sulfides can be explained by lack of such an upgrading process for the sulfide due to their distal locations in a migrating conduit.

  13. Chalcophile element (Ni, Cu, PGE, and Au) variations in the Tamarack magmatic sulfide deposit in the Midcontinent Rift System: implications for dynamic ore-forming processes

    Science.gov (United States)

    Taranovic, Valentina; Ripley, Edward M.; Li, Chusi; Rossell, Dean

    2016-03-01

    The Tamarack magmatic sulfide deposit is hosted by the Tamarack Intrusive Complex (1105.6 ± 1.2 Ma) in the Midcontinent Rift System. The most important sulfide mineralization in the Complex occurs in the northern part, which consists of two separate intrusive units: an early funnel-shaped layered peridotite body containing relatively fine-grained olivine (referred to as the FGO Intrusion) at the top, and a late gabbro-troctolite-peridotite dike-like body containing relatively coarse-grained olivine (referred to as the CGO Intrusion) at the bottom. Disseminated, net-textured, and massive sulfides occur in the base of the FGO Intrusion as well as in the upper part of the CGO Intrusion. The widest part of the CGO Intrusion also hosts a large semi-massive (net-textured) sulfide ore body locally surrounded by disseminated sulfide mineralization. Small massive sulfide veins occur in the footwall of the FGO Intrusion and in the wall rocks of the CGO dike. The sulfide mineralization is predominantly composed of pyrrhotite, pentlandite, and chalcopyrite, plus minor magnetite. Pyrrhotite containing the highest Ni and Co contents occurs in the FGO disseminated sulfides and in the CGO semi-massive sulfide ores, respectively. The most important platinum-group minerals associated with the base metal sulfides are sperrylite (PtAs2), sudburyite (PdSb), and michenerite (PdBiTe). Nickel shows a strong positive correlation with S in all types of sulfide mineralization, and Cu shows a strong positive correlation with S in the disseminated sulfide mineralization. At a given S content, the concentrations of Pt, Pd, and Au in the CGO disseminated sulfides are significantly higher than those in the FGO disseminated sulfides. The semi-massive sulfide ores are characterized by significantly higher IPGE (Ir, Os, Ru, and Rh) concentrations than most of the massive sulfide ores. With few exceptions, all of the various textural types of sulfide mineralization collectively show a good positive correlation between Pt and Pd, and between individual IPGE. At a given Pt or Pd content, however, the semi-massive sulfide ores have higher IPGE contents than the disseminated sulfide samples. Modeling results show that the variations in PGE tenors (metals in recalculated 100 % sulfide) in the Tamarack magmatic sulfide deposit are mainly controlled by variable R factors (magma/sulfide-liquid mass ratios) during sulfide-liquid segregation and subsequent monosulfide solid solution (MSS) fractionation during cooling. The initial contents of Ir, Pt, and Pd in the parental magma, estimated from the metal tenors of the disseminated sulfides, are 0.2, 2, and 1.8 ppb, respectively, which are ˜1/5 of the values for the PGE-undepleted primitive basalts of the Midcontinent Rift System. The variations of PGE tenors in the semi-massive and massive sulfide ores can be explained by MSS fractional crystallization from sulfide liquids. Extreme variations in the PGE contents of the massive sulfides may also in part reflect metal mobility during post-crystallization hydrothermal processes. The higher PGE tenors for the disseminated sulfides in the CGO dike relative to those in the FGO Intrusion are consistent with formation in a dynamic conduit where the early sulfide liquids left in the conduit by the FGO magma were subsequently upgraded by the subsequent surge of the CGO magma. The relatively low PGE tenors for the semi-massive and massive sulfides can be explained by lack of such an upgrading process for the sulfide due to their distal locations in a migrating conduit.

  14. Trace elements concentrations (Zn, Cu, Pb, Cd, As and Hg in the Mediterranean mussel (Mytilus galloprovincialis and evaluation of mussel quality and possible human health risk from cultivated and wild sites of the southeastern Adriatic Sea, Montenegro

    Directory of Open Access Journals (Sweden)

    Jović Mihajlo

    2011-01-01

    Full Text Available The Mediterranean mussel Mytilus galloprovincialis (L was collected from the fall 2005 to the winter 2009 from the six sites on the Montenegrin coastline. Two wild samples were collected from the open sea coastline, and two cultivated and two wild were from the Boka Kotorska Bay. The mussels soft tissue was analyzed for zinc (Zn, copper (Cu, lead (Pb, cadmium (Cd, arsenic (As and total mercury (Hg. Concentrations of these metals ranged from 135.5-210 for Zn, 6.2-14.5 for Cu, 4.0-11.5 for Pb, 1.7-2.1 for Cd, 5.8-12.4 for As and 0.11-0.51 for Hg, in mg kg-1 dry weight. The metals were found to be present in the samples at different levels, but not in concentrations higher than maximum residual levels prescribed by the European Union (EU and US Food and Drug Administration (USFDA regulations for seafood. This indicates that the consumption of wild or cultivated mussels from the studied area is safe in moderate quantities.

  15. Mercury (Hg) accumulation in terrestrial carbon (C) reservoirs: magnitude, spatial patterns, fate upon C losses, and implications of global change

    Science.gov (United States)

    Obrist, D.; Johnson, D. W.; Lindberg, S. E.; Luo, Y.

    2012-04-01

    Terrestrial ecosystems are strong natural reservoirs that retain the bulk of atmospheric Hg deposition. As a result, a long-term legacy of past and present Hg pollution is sequestered in surface litter and soil pools. Hg shows a particular affinity to—and hence tends to accumulate in—terrestrial organic C. We present a summary of a comprehensive five-year investigation where we quantified: (i) relationships between Hg and C across 14 forests sites to assess the affinity of Hg to C accumulation across spatial scales; (ii) the degree to which C determines net retention and spatial accumulation of Hg; (iii) the fate of Hg upon losses of C, including losses though wildfires and mineralization; (iv) the coupling of gaseous Hg losses to CO2 respiration; and (v) the potential sensitivity of climate-change induced changes in C on terrestrial Hg sequestration. Results show that continental-scale spatial distribution of Hg in soils and litter is strongly related to C, and that old terrestrial C pools (as determined by C/N ratios) are particularly prone to Hg enrichment. The correlation of Hg and C is likely responsible for increasing Hg levels (concentrations and pools of total Hg, as well as methylated Hg) with higher latitude, which we attribute to a legacy of Hg sequestration in C-rich layers of northern ecosystems. Experimental studies and field observations to address fate of Hg sequestered in organic C show that: (i) fires leads to up-to-complete Hg losses in either gaseous elemental or particulate-bound form; (ii) litter decomposition also leads to evasion losses of Hg in the range of 50% of initial Hg, but little Hg is subject to runoff as dissolved Hg; (iii) soils effectively retain Hg with only about 3% of Hg subject to volatilization upon C loss during respiration; (iv) no links between CO2 and gaseous Hg concentrations are observed in soil depth profiles in the field, indicating that fate and movement of gaseous Hg is decoupled from that of CO2. We calculate

  16. High-resolution Hg Chemostratigraphy

    DEFF Research Database (Denmark)

    Sial, Alcides N.; Chen, J.; Lacerda, L.D.;

    2014-01-01

    There is a renewed interest in volcanism as the major trigger for dramatic climatic changes at the Cretaceous–Paleogene transition (KTB), which were accompanied by a decrease in biodiversity and mass extinction. We have used Hg contents as proxy for volcanic activity at the classical localities o...

  17. Contrasting food web factor and body size relationships with Hg and Se concentrations in marine biota.

    Directory of Open Access Journals (Sweden)

    Roxanne Karimi

    Full Text Available Marine fish and shellfish are primary sources of human exposure to mercury, a potentially toxic metal, and selenium, an essential element that may protect against mercury bioaccumulation and toxicity. Yet we lack a thorough understanding of Hg and Se patterns in common marine taxa, particularly those that are commercially important, and how food web and body size factors differ in their influence on Hg and Se patterns. We compared Hg and Se content among marine fish and invertebrate taxa collected from Long Island, NY, and examined associations between Hg, Se, body length, trophic level (measured by δ(15N and degree of pelagic feeding (measured by δ(13C. Finfish, particularly shark, had high Hg content whereas bivalves generally had high Se content. Both taxonomic differences and variability were larger for Hg than Se, and Hg content explained most of the variation in Hg:Se molar ratios among taxa. Finally, Hg was more strongly associated with length and trophic level across taxa than Se, consistent with a greater degree of Hg bioaccumulation in the body over time, and biomagnification through the food web, respectively. Overall, our findings indicate distinct taxonomic and ecological Hg and Se patterns in commercially important marine biota, and these patterns have nutritional and toxicological implications for seafood-consuming wildlife and humans.

  18. Contrasting food web factor and body size relationships with Hg and Se concentrations in marine biota.

    Science.gov (United States)

    Karimi, Roxanne; Frisk, Michael; Fisher, Nicholas S

    2013-01-01

    Marine fish and shellfish are primary sources of human exposure to mercury, a potentially toxic metal, and selenium, an essential element that may protect against mercury bioaccumulation and toxicity. Yet we lack a thorough understanding of Hg and Se patterns in common marine taxa, particularly those that are commercially important, and how food web and body size factors differ in their influence on Hg and Se patterns. We compared Hg and Se content among marine fish and invertebrate taxa collected from Long Island, NY, and examined associations between Hg, Se, body length, trophic level (measured by δ(15)N) and degree of pelagic feeding (measured by δ(13)C). Finfish, particularly shark, had high Hg content whereas bivalves generally had high Se content. Both taxonomic differences and variability were larger for Hg than Se, and Hg content explained most of the variation in Hg:Se molar ratios among taxa. Finally, Hg was more strongly associated with length and trophic level across taxa than Se, consistent with a greater degree of Hg bioaccumulation in the body over time, and biomagnification through the food web, respectively. Overall, our findings indicate distinct taxonomic and ecological Hg and Se patterns in commercially important marine biota, and these patterns have nutritional and toxicological implications for seafood-consuming wildlife and humans. PMID:24019976

  19. The new barium zinc mercurides Ba3ZnHg10 and BaZn0.6Hg3.4 – Synthesis, crystal and electronic structure

    International Nuclear Information System (INIS)

    The title compounds Ba3ZnHg10 and BaZn0.6Hg3.4 were synthesized from stoichiometric ratios of the elements in Ta crucibles. Their crystal structures, which both represent new structure types, have been determined using single crystal X-ray data. The structure of Ba3ZnHg10 (orthorhombic, oP28, space group Pmmn, a=701.2(3), b=1706.9(8), c=627.3(3)pm, Z=2, R1=0.0657) contains folded 44 Hg nets, where the meshes form the bases of flat rectangular pyramids resembling the structure of BaAl4. The flat pyramids are connected via Hg–Zn/Hg bonds, leaving large channels at the folds, in which Ba(1) and Hg(2) atoms alternate. Whereas the remaining Hg/Zn atoms form a covalent 3D network of three- to five-bonded atoms with short M–M distances (273–301 pm; CN 9–11), the Hg(2) atoms in the channels adopt a comparatively large coordination number of 12 and increased distances (317–348 pm) to their Zn/Hg neighbours. In the structure of BaZn0.6Hg3.4 (cubic, cI320, space group I4¯3d, a=2025.50(7) pm, Z=64, R1=0.0440), with a chemical composition not much different from that of Ba3ZnHg10, the Zn/Hg atoms of the mixed positions M(1/2) are arranged in an slightly distorted primitive cubic lattice with a 4×4×4 subcell relation to the unit cell. The 24 of the originating 64 cubes contain planar cis tetramers Hg(5,6)4 with Hg in a nearly trigonal planar or tetrahedral coordination. In another 24 of the small cubes, two opposing faces are decorated by Hg(3,4)2 dumbbells, two by Ba(2) atoms respectively. The third type of small cubes are centered by Ba(1) atoms only. The complex 3D polyanionic Hg/Zn network thus formed is compared with the Hg partial structure in Rb3Hg20 applying a group-subgroup relation. Despite their different overall structures, the connectivity of the negatively charged Hg atoms, the rather metallic Zn bonding characteristic (as obtained from FP-LAPW band structure calculations) and the coordination number of 16 for all Ba cations relate the two title

  20. Changements de phases durant l'électrolyse des systèmes Hg-Tl, Hg-Sn, Hg-Pb et Hg-Zn

    OpenAIRE

    Dumas, Jean-Pierre; Bougarfa, L.; Bensaid, J.

    1984-01-01

    On utilise la méthode électrochimique de détection des transformations de phases dans les amalgames au cours d'électrolyse monotherme décrite dans un article précédent [2] pour l'étude des systèmes Hg-Tl, Hg-Sn, Hg-Pb et Hg-Zn. Dans les systèmes Hg-Pb et Hg-Zn la cristallisation se produit dès que la fraction molaire de saturation est atteinte mais des phases liquides métastables sont observées dans les systèmes Hg-Tl et Hg-Sn. A 25 °C, la rupture de métastabilité a lieu à des fractions molai...

  1. Theranostic mercury: 197(m)Hg with high specific activity for imaging and therapy

    International Nuclear Information System (INIS)

    The no carrier added (NCA) radionuclide 197(m)Hg is accessible through proton induced nuclear reactions on gold. The decay properties of both simultaneous produced nuclear isomers 197mHg and 197Hg like convenient half life, low energy gamma radiations for imaging, Auger and conversion electrons for therapy are combined with unique chemical and physical properties of mercury and its compounds. Gold as a monoisotopic element has a natural abundance of 100% 197Au superseding expensive enrichment for the target material. Additionally, the high thermal conductivity of gold enables high beam current irradiations. For separation of target material a liquid–liquid extraction method was applied. - Highlights: • No carrier added 197(m)Hg. • 197(m)Hg promising for therapeutic application. • 197(m)Hg for imaging

  2. Bioaccumulation of Hg in the mushroom Pleurotus ostreatus

    Energy Technology Data Exchange (ETDEWEB)

    Bressa, G.; Cima, L.; Costa, P.

    1988-10-01

    The possibility of utilizing industrial, urban, and other wastes for the growth of a product which is directly edible by humans is fascinating. However, it is possible that many wastes containing toxic substances, for example, heavy metals, could reach the food chain and produce adverse effects on human health. To this end, we studied the possibility of bioaccumulation of Hg by a mushroom, Pleurotus ostreatus, grown on an artificial compost containing this element. Concentrations of 0.05, 0.1, and 0.2 mg/kg of Hg as Hg(NO/sub 3/)/sub 2/.H/sub 2/O were added to three groups of the same compost, successively inoculated with the mycelia of the mushroom. Higher concentrations strongly reduced the growth of the mycelia and therefore were not utilized. The concentrations of Hg in the substrate and in the mushroom were evaluated by AAS. The range of the accumulation factor was found to be 65-140, i.e., very marked. This finding suggests that the cultivation of P. ostreatus on substrates containing Hg from industrial and urban wastes could involve possible risks to human health.

  3. Spectroscopic variability and magnetic fields of HgMn stars

    CERN Document Server

    Hubrig, S; Ilyin, I; Korhonen, H; Savanov, I S; Dall, T; Schoeller, M; Cowley, C R; Briquet, M; Arlt, R

    2011-01-01

    The discovery of exotic abundances, chemical inhomogeneities, and weak magnetic fields on the surface of late B-type primaries in spectroscopic binaries has important implications not only for our understanding of the formation mechanisms of stars with Hg and Mn peculiarities themselves, but also for the general understanding of B-type star formation in binary systems. The origin of the abundance anomalies observed in late B-type stars with HgMn peculiarity is still poorly understood. The connection between HgMn peculiarity and membership in binary and multiple systems is supported by our observations during the last decade. The important result achieved in our studies of a large sample of HgMn stars is the finding that most HgMn stars exhibit spectral variability of various chemical elements, proving that the presence of an inhomogeneous distribution on the surface of these stars is a rather common characteristic and not a rare phenomenon. Further, in the studied systems, we found that all components are che...

  4. Mercury isotope signatures as tracers for Hg cycling at the New Idria Hg mine.

    Science.gov (United States)

    Wiederhold, Jan G; Smith, Robin S; Siebner, Hagar; Jew, Adam D; Brown, Gordon E; Bourdon, Bernard; Kretzschmar, Ruben

    2013-06-18

    Mass-dependent fractionation (MDF) and mass-independent fractionation (MIF) of Hg isotopes provides a new tool for tracing Hg in contaminated environments such as mining sites, which represent major point sources of Hg pollution into surrounding ecosystems. Here, we present Hg isotope ratios of unroasted ore waste, calcine (roasted ore), and poplar leaves collected at a closed Hg mine (New Idria, CA, U.S.A.). Unroasted ore waste was isotopically uniform with δ(202)Hg values from -0.09 to 0.16‰ (± 0.10‰, 2 SD), close to the estimated initial composition of the HgS ore (-0.26‰). In contrast, calcine samples exhibited variable δ(202)Hg values ranging from -1.91‰ to +2.10‰. Small MIF signatures in the calcine were consistent with nuclear volume fractionation of Hg isotopes during or after the roasting process. The poplar leaves exhibited negative MDF (-3.18 to -1.22‰) and small positive MIF values (Δ(199)Hg of 0.02 to 0.21‰). Sequential extractions combined with Hg isotope analysis revealed higher δ(202)Hg values for the more soluble Hg pools in calcines compared with residual HgS phases. Our data provide novel insights into possible in situ transformations of Hg phases and suggest that isotopically heavy secondary Hg phases were formed in the calcine, which will influence the isotope composition of Hg leached from the site. PMID:23662941

  5. Hg(0) Removal Using Se(0)-doped Montmorillonite from Selenite(IV)

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Jooyoup [Univ. of Cincinnati, Ohio (United States); Kim, Yongjin [Korea Institute of Industrial Technology, Chonan (Korea, Republic of)

    2013-12-15

    Potassium methylselenite (KSeO{sub 2}(OCH{sub 3})) was reduced to elemental selenium, Se(0), and then doped onto montmorillonite K 10 (MK10) clay to examine the interaction between elemental mercury (Hg(0)) vapor and Se(0) in an effort to understand the possible heterogeneous reaction of Hg(0) vapor and Se(0) solid. The clay was used as a cost-effective support material for uniform dispersion of Se(0). The Se(0)-doped MK10 showed an excellent reaction performance with Hg(0) under an inert nitrogen gas at 70 and 140 .deg. C in our lab-scale fixed-bed system. However, the precursor, KSeO{sub 2}(OCH{sub 3})-doped MK10 showed a negligible reaction performance with Hg(0), suggesting that the oxidation state of selenium plays a key role in the reaction of Hg(0) vapor and selenium compounds.

  6. Detection Feasibility of Magnetic Fields and HG Abundances in HgMn Stars

    Science.gov (United States)

    Takada-Hidai, M.; Sakaue, A.; Kotake, J.

    We analyzed two Fe II lines at 6147.7 AA and 6149.2 AA observed in 14 HgMn stars with the purpose to examine the feasibility of detecting magnetic fields in HgMn stars based on Mathys' empirical relation between the strengths of the Fe II lines and magnetic fields (Mathys 1990, A&A 232, 151). Takada-Hidai & Jugaku (1992, PASP 104, 106) found that the Fe II 6149 AA is strongly blended with the Hg II 6149.5 AA line in the typical HgMn star mu Lep. To investigate the blending effect of the Hg II line, we measured the strengths of Fe II lines in the sample stars with the Hg abundances of 4 < log Hg < 7 and obtained Hg abundaces from the blending Hg II lines. Most of the resulting Hg abundances were found to agree with the previously determined values within about 0.6 dex. We also found, from a comparison between the strengths of Fe II lines with Hg abundances, that the blending effect of the Hg II line seems to be negligible for the Hg abundances of about < 5 dex, and therefore magnetic fields may possibly be detected with Mathys' empirical relation in case of HgMn stars with such Hg abundances as < 5 dex.

  7. Hg transfer from contaminated soils to plants and animals

    NARCIS (Netherlands)

    Rodrigues, S.M.; Henriques, B.; Reis, A.T.; Duarte, A.C.; Pereira, E.; Romkens, P.F.A.M.

    2012-01-01

    Understanding the transfer of mercury (Hg) from soil to crops is crucial due to Hg toxicity and Hg occurrence in terrestrial systems. Previous research has shown that available Hg in soils contributes to plant Hg levels. Plant Hg concentrations are related to soil conditions and plant characteristic

  8. PENCEMARAN LOGAM BERAT MERKURI (Hg PADA AIRTANAH

    Directory of Open Access Journals (Sweden)

    Thomas Triadi Putranto

    2012-02-01

    Full Text Available The earth consists largely of water because the land area is smaller than the ocean. Human beings on this earthcan not escape the need for water. Water is the main requirement for the process of life on the earth.Relatively clean water that is coveted by men, whether for purposes of daily life, for industrial purposes, for thecleanliness of city sanitation, as well as for agricultural purposes and so forth. Heavy metal pollution is a veryserious issue to be handled, because of adverse environmental and ecosystem in general. Heavy metallic elementis the element which has a density of more than 5 gr/cm3. Hg has a density of 13.55 gr/cm3. Disaster is anoutbreak of Minamata mercury poisoning in people who eat fish contaminated by mercury in Minamata Japan,and this event is known as Minamata Disease. Efforts to tackle the heavy metal pollution can actually be doneusing a chemical process or by microorganism such as microbes and bacteria.

  9. Responses of membrane protection enzyme system of tobacco leaves on Hg, Cd and Pb stresses in soil.

    Science.gov (United States)

    Yan, Chong Ling; Lin, Peng; Wang, Xiao Rong

    2002-09-01

    Pot experiment was used to study the responses of membrane protection enzyme system of tobacco leaves on Hg, Cd and Pb stresses in soil. The results showed that POD activity gradually increased with increasing concetrations of Hg, Cd and Pb. CAT and SOD activity gradually decreased under three heavy metals common existing and SOD variation curve showed unimodal curve under single or two elements existing with increase of concentration of Hg, Cd and Pb. The effects of Hg, Cd and Pb in soil: three elemets together > two elements together > single element only. The effects resulted in an imbalance--activated oxygen produce and scavenge and physiological biochemical process disorder. There was a synergistic action for the effect of Hg, Cd and Pb in soil on membrane protection enzyme system in tobacco leaves.

  10. Hg and As Minerals in Fluid Inclusions from the Williams Mine, Hemlo, and Their Genetic Implications

    Institute of Scientific and Technical Information of China (English)

    LU HUANZHANG(卢焕章); JAYANTA. GUHA; DON. C. HARRIS

    2002-01-01

    The Hemlo mineralization is enigmatic compared to general Archean lode gold deposits based on the fact that it is characterized by an exotic mineralogy containing elements such as As, Hg, Sb, Ba, V and Mo. The genetic concepts range from syngenetic to epigenetic types of mineralization. This reconnaissance study was designed to examine the relationship of Hg-As minerals with respect to fluid inclusions in the Williams mine (formerly known as the Page Williams mine) covering the A and C ore zones.

  11. Chemical stabilization and high pressure synthesis of Ba-free Hg-based superconductors, (Hg,M)Sr{sub 2}Ca{sub n-1}Cu{sub n}O{sub y}(N=1{approximately}3)

    Energy Technology Data Exchange (ETDEWEB)

    Kishio, K. [Univ. of Tokyo (Japan)]|[Kyoto Univ. (Japan); Shimoyama, J.; Hahakura, S. [Univ. of Tokyo (Japan)] [and others

    1994-12-31

    A homologous series of new Hg-based HTSC compounds, (Hg,M)Sr{sub 2}Ca{sub n-1}Cu{sub n}O{sub y} with n=1 to 3, have been synthesized. The stabilization of the pure phases have been accomplished by chemical doping of third elements such as M=Cr, Mo and Re. While the Hg1201(n=1) phase was readily obtained in this way, it was necessary to simultaneously dope Y into the Ca site to stabilize the Hg1212(n=2) phase. On the other hand, single-phase Y-free Hg1212(n=2) and Hg1223(n=3) samples were synthesized only under a high pressure of 6 GPa. In sharp contrast to the Ba-containing compounds, all the samples prepared in the present study have been quite stable during the synthesis and no deterioration in air has been observed after the preparation.

  12. Distribution and air-sea exchange of mercury (Hg in the Yellow Sea

    Directory of Open Access Journals (Sweden)

    Z. J. Ci

    2011-01-01

    Full Text Available The Yellow Sea, surrounded by East China and the Korea Peninsula, is a potentially important receptor for anthropogenic mercury (Hg emissions from East Asia. However, there is little documentation about the distribution and cycle of Hg in this marine system. During the cruise covering the Yellow Sea in July 2010, gaseous elemental mercury (GEM or Hg(0 in the atmosphere, total Hg (THg, reactive Hg (RHg and dissolved gaseous mercury (DGM, largely Hg(0 in the waters were measured aboard the R/V Kexue III. The mean (±SD concentration of GEM over the entire cruise was 2.61±0.50 ng m−3 (range: 1.68 to 4.34 ng m−3, which were generally higher than other open oceans. The spatial distribution of GEM generally reflected a clear gradient with high levels near the coast of East China and low levels in open waters, suggesting the significant atmospheric Hg outflow from East China. The mean concentration of THg in the surface waters was 1.69±0.35 ng l−1 and the RHg accounted for a considerable fraction of THg (RHg: 1.08±0.28 ng l−1, %RHg/THg=63.9%. The mean concentration of DGM in the surface waters was 63.9±13.7 pg l−1 and always suggested the supersaturation of Hg(0 in the surface waters with respect to Hg(0 in the atmosphere (the degree of saturation: 7.83±2.29 with a range of 3.58–14.00. The mean Hg(0 flux at the air-sea interface was estimated to be 22.58±14.56 ng m−2 h−1 based on a two-layer exchange model. The high wind speed and DGM levels induced the extremely high Hg(0 emission rates. Measurements at three selected stations showed no clear vertical patterns of all three species of Hg in the water column. Overall, the elevated Hg levels in the Yellow Sea compared with other open oceans suggested that the human activity has significantly influenced the oceanic Hg cycle downwind of East Asia.

  13. Mercury methylation and reduction potentials in marine water: An improved methodology using {sup 197}Hg radiotracer

    Energy Technology Data Exchange (ETDEWEB)

    Koron, Neza [National Institute of Biology, Marine Biology Station, Fornace 41, 6330 Piran (Slovenia); Bratkic, Arne [Department of Environmental Sciences, ' Jozef Stefan' Institute, Jamova 39, 1000 Ljubljana (Slovenia); Ribeiro Guevara, Sergio, E-mail: ribeiro@cab.cnea.gov.ar [Laboratorio de Analisis por Activacion Neutronica, Centro Atomico Bariloche, Av. Bustillo km 9.5, 8400 Bariloche (Argentina); Vahcic, Mitja; Horvat, Milena [Department of Environmental Sciences, ' Jozef Stefan' Institute, Jamova 39, 1000 Ljubljana (Slovenia)

    2012-01-15

    A highly sensitive laboratory methodology for simultaneous determination of methylation and reduction of spiked inorganic mercury (Hg{sup 2+}) in marine water labelled with high specific activity radiotracer ({sup 197}Hg prepared from enriched {sup 196}Hg stable isotope) was developed. A conventional extraction protocol for methylmercury (CH{sub 3}Hg{sup +}) was modified in order to significantly reduce the partitioning of interfering labelled Hg{sup 2+} into the final extract, thus allowing the detection of as little as 0.1% of the Hg{sup 2+} spike transformed to labelled CH{sub 3}Hg{sup +}. The efficiency of the modified CH{sub 3}Hg{sup +} extraction procedure was assessed by radiolabelled CH{sub 3}Hg{sup +} spikes corresponding to concentrations of methylmercury between 0.05 and 4 ng L{sup -1}. The recoveries were 73.0{+-}6.0% and 77.5{+-}3.9% for marine and MilliQ water, respectively. The reduction potential was assessed by purging and trapping the radiolabelled elemental Hg in a permanganate solution. The method allows detection of the reduction of as little as 0.001% of labelled Hg{sup 2+} spiked to natural waters. To our knowledge, the optimised methodology is among the most sensitive available to study the Hg methylation and reduction potential, therefore allowing experiments to be done at spikes close to natural levels (1-10 ng L{sup -1}). - Highlights: Black-Right-Pointing-Pointer Inorganic mercury methylation and reduction in marine water were studied. Black-Right-Pointing-Pointer High specific activity {sup 197}Hg was used to label Hg{sup 2+} spikes at natural levels. Black-Right-Pointing-Pointer Methylmercury extraction had 73% efficiency for 0.05-4 ng L{sup -1} levels. Black-Right-Pointing-Pointer High sensibility to assess methylation potentials, below 0.1% of the spike. Black-Right-Pointing-Pointer High sensibility also for reduction potentials, as low as 0.001% of the spike.

  14. Investigation of Hg uptake and transport between paddy soil and rice seeds combining Hg isotopic composition and speciation

    Directory of Open Access Journals (Sweden)

    C. Feng

    2016-02-01

    Full Text Available Abstract Human consumption of rice constitutes a potential toxicological risk in mercury (Hg polluted areas such as Hg mining regions in China. It is recognized to be an important source of Hg for the local human diet considering the efficient bioaccumulation of methylmercury (MeHg in rice seed. To assess Hg sources and uptake pathways to the rice plants, Hg speciation and isotopic composition were investigated in rice seeds and their corresponding paddy soils from different locations within the Wanshan Hg mining area (Guizhou Province, China. A large variation of Hg speciation is observed in rice seeds and paddy soils irrespective of the sampling location. Mass dependent fractionation (MDF of Hg in rice seeds differs by up to ∼4.0 ‰ in δ202Hg values, while mass independent fractionation (MIF of Hg isotopes remains constant (Δ199Hg ∼ 0‰. Hg isotopic composition in rice seeds covaries with that of paddy soils but exhibits lighter isotopic signature (δ202Hg. Such isotopic offset is mainly attributed to plant uptake and translocation processes. Also, seeds containing higher MeHg (MeHg/total Hg > 50% have significantly heavier Hg isotopes suggesting that MeHg uptake and transport to the seed in such rice plants is facilitated compared to inorganic Hg.

  15. 46 CFR 53.05-1 - Safety valve requirements for steam boilers (modifies HG-400 and HG-401).

    Science.gov (United States)

    2010-10-01

    ... 46 Shipping 2 2010-10-01 2010-10-01 false Safety valve requirements for steam boilers (modifies HG... requirements for steam boilers (modifies HG-400 and HG-401). (a) The pressure relief valve requirements and the safety valve requirements for steam boilers must be as indicated in HG-400 and HG-401 of section IV...

  16. HgCdTe APDs for free space optical communications

    Science.gov (United States)

    Rothman, J.; Lasfargues, G.; Abergel, J.

    2015-10-01

    HgCdTe avalanche photodiode single element detectors have been developed for a large scope of photon starved applications. The present communication is dedicated to use of these detectors for free space optical communications. In this perspective we present and discuss the sensitivity and bandwidth that has been measured directly on HgCdTe APDs and on detector modules. In particular, we report on the performance of TEC cooled large area detectors with sensitive diameters ranging from 30- 200 μm, characterised by detector gains of 2- 20 V/μW and noise equivalent input power of 0.1-1 nW for bandwidths ranging from 20 to 400 MHz. One of these detectors has been used during the lunar laser communication demonstration (LLCD) and the results The perspectives for high data rate transmission is estimated from the results of impulse response measurements on HgCdTe APDs. These results indicate that bandwidths close to 10 GHz can be achieved in these devices. The associated sensitivity at an APD gain of 100 is estimated to be below 4 photons rms (NEP<10 nW) for APDs operated at 300 K.

  17. HgTe-CdTe SUPERLATTICES

    OpenAIRE

    Smith, D.; Mcgill, T.

    1984-01-01

    We report on a theoretical study of the electronic properties of HgTe-CdTe superlattices. The band gap as a function of layer thickness, effective masses normal to the layer plane and tunneling length are compared to the corresponding (Hg, Cd)Te alloys. We find that the superlattice possesses a number of properties that may make it superior to the corresponding alloy as an infrared material.

  18. Identifying Key Proteins in Hg Methylation Pathways of Desulfovibrio by Global Proteomics, Final Technical Report

    Energy Technology Data Exchange (ETDEWEB)

    Summers, Anne O. [Univ. of Georgia, Athens, GA (United States). Dept. of Microbiology; Miller, Susan M. [Univ. of California, San Francisco, CA (United States). Dept. of Pharmaceutical Chemistry; Wall, Judy [Univ. of Missouri, Columbia, MO (United States). Dept. of Biochemistry; Lipton, Mary [Pacific Northwest National Lab. (PNNL), Richland, WA (United States)

    2016-06-18

    Elemental mercury, Hg(0) is a contaminant at many DOE sites, especially at Oak Ridge National Laboratory (ORNL) where the spread of spilled Hg and its effects on microbial populations have been monitored for decades. To explore the microbial interactions with Hg, we have devised a global proteomic approach capable of directly detecting Hg-adducts of proteins. This technique developed in the facultative anaerobe, Escherichia coli, allows us to identify the proteins most vulnerable to acute exposure to organomercurials phenyl- and ethyl-mercury (as surrogates for the highly neurotoxic methyl-Hg) (Polacco, et al, 2011). We have found >300 such proteins in all metabolic functional groups and cellular compartments; most are highly conserved and can serve as markers for acute Hg exposure (Zink, et al. 2016, in preparation). We have also discovered that acute Hg exposure severely disrupts thiol, iron and redox homeostases, and electrolyte balance (LaVoie, et al., 2015) Thus, we proposed to bring these techniques to bear on the central problem of identifying the cellular proteins involved in bacterial uptake and methylation of mercury and its release from the cell.

  19. Identifying Key Proteins in Hg Methylation Pathways of Desulfovibrio by Global Proteomics

    Energy Technology Data Exchange (ETDEWEB)

    Summers, Anne O. [University of Georgia

    2016-06-18

    Elemental mercury, Hg(0) is a contaminant at many DOE sites, especially at Oak Ridge National Laboratory (ORNL) where the spread of spilled Hg and its effects on microbial populations have been monitored for decades. To explore the microbial interactions with Hg, we have devised a global proteomic approach capable of directly detecting Hg-adducts of proteins. This technique developed in the facultative anaerobe, Escherichia coli, allows us to identify the proteins most vulnerable to acute exposure to organomercurials phenyl- and ethyl-mercury (as surrogates for the highly neurotoxic methyl-Hg) (Polacco, et al, 2011). We have found >300 such proteins in all metabolic functional groups and cellular compartments; most are highly conserved and can serve as markers for acute Hg exposure (Zink, et al. 2016, in preparation). We have also discovered that acute Hg exposure severely disrupts thiol, iron and redox homeostases, and electrolyte balance (LaVoie, et al., 2015) Thus, we proposed to bring these techniques to bear on the central problem of identifying the cellular proteins involved in bacterial uptake and methylation of mercury and its release from the cell.

  20. Experimental study on Hg0 removal from flue gas over columnar MnOx-CeO2/activated coke

    Science.gov (United States)

    Xie, Yine; Li, Caiting; Zhao, Lingkui; Zhang, Jie; Zeng, Guangming; Zhang, Xunan; Zhang, Wei; Tao, Shasha

    2015-04-01

    Mn-Ce mixed oxides supported on commercial columnar activated coke (MnCe/AC) were employed to remove elemental mercury (Hg0) at low temperatures (100-250 °C) without the assistance of HCl in flue gas. The samples were characterized by X-ray diffraction (XRD), Brunauer-Emmett-Teller (BET), X-ray photoelectron spectroscopy (XPS) and temperature programmed desorption (TPD). Effects of some factors, including Mn-Ce loading values, active component, reaction temperatures and flue gas components (O2, SO2, NO, H2O), on Hg0 removal efficiency were investigated. Results indicated that the optimal Mn-Ce loading value and reaction temperature were 6% and 190 °C, respectively. Considerable high Hg0 removal efficiency (>90%) can be obtained over MnCe6/AC under both N2/O2 atmosphere and simulated flue gas atmosphere at 190 °C. Besides, it was observed that O2 and NO exerted a promotional effect on Hg0 removal, H2O exhibited a suppressive effect, and SO2 hindered Hg0 removal seriously when in the absence of O2. Furthermore, the XPS spectra of Hg 4f and Hg-TPD results showed that the captured mercury were existed as Hg0 and HgO on the MnCe6/AC, and HgO was the major species, which illustrated that adsorption and catalytic oxidation process were included for Hg0 removal over MnCe6/AC, and catalytic oxidation played the critical role. What's more, both lattice oxygen and chemisorbed oxygen or OH groups on MnCe6/AC contributed to Hg0 oxidation. MnCe6/AC, which exhibited excellent performance on Hg0 removal in the absence of HCl, appeared to be promising in industrial application, especially for low-rank coal fired flue gas.

  1. Isotopic Hg in an Allende carbon-rich residue

    Science.gov (United States)

    Reed, G. W., Jr.; Jovanovic, S.

    1990-01-01

    A carbon-rich residue from Allende subjected to stepwise heating yielded two isotopically resolvable types of Hg: one with an (Hg-196)/(Hg-202) concentration ratio the same as terrestrial (monitor) Hg; the other enriched in Hg-196 relative to Hg-202 by about 60 percent. Hg with the 202 isotope enriched relative to 196, as is found in bulk Allende, was not observed. Whether the result of mass fractionation or nucleosynthesis, the distinct types of Hg entered different carrier phases and were not thermally mobilized since the accretion of the Allende parent body.

  2. Complexation of Hg with phytochelatins is important for plant Hg tolerance.

    Science.gov (United States)

    Carrasco-Gil, Sandra; Alvarez-Fernández, Ana; Sobrino-Plata, Juan; Millán, Rocío; Carpena-Ruiz, Ramón O; Leduc, Danika L; Andrews, Joy C; Abadía, Javier; Hernández, Luís E

    2011-05-01

    Three-week-old alfalfa (Medicago sativa), barley (Hordeum vulgare) and maize (Zea mays) were exposed for 7 d to 30 µm of mercury (HgCl(2) ) to characterize the Hg speciation in root, with no symptoms of being poisoned. The largest pool (99%) was associated with the particulate fraction, whereas the soluble fraction (SF) accounted for a minor proportion (phytochelatins (PCs) in root SF, which was particularly varied in alfalfa (eight ligands and five stoichiometries), a species that also accumulated homophytochelatins. Spatial localization of Hg in alfalfa roots by microprobe synchrotron X-ray fluorescence spectroscopy showed that most of the Hg co-localized with sulphur in the vascular cylinder. Extended X-ray Absorption Fine Structure (EXAFS) fingerprint fitting revealed that Hg was bound in vivo to organic-S compounds, i.e. biomolecules containing cysteine. Albeit a minor proportion of total Hg, Hg-PCs complexes in the SF might be important for tolerance to Hg, as was found with Arabidopsis thaliana mutants cad2-1 (with low glutathione content) and cad1-3 (unable to synthesize PCs) in comparison with wild type plants. Interestingly, high-performance liquid chromatography-electrospray ionization-time of flight analysis showed that none of these mutants accumulated Hg-biothiol complexes.

  3. Distribution and air-sea exchange of mercury (Hg in the Yellow Sea

    Directory of Open Access Journals (Sweden)

    Z. J. Ci

    2011-03-01

    Full Text Available The Yellow Sea, surrounded by East China and the Korea Peninsula, is a potentially important receptor for anthropogenic mercury (Hg emissions from East Asia. However, there is little documentation about the distribution and cycle of Hg in this marine system. During the cruise covering the Yellow Sea in July 2010, gaseous elemental mercury (GEM or Hg(0 in the atmosphere, total Hg (THg, reactive Hg (RHg and dissolved gaseous mercury (DGM, largely Hg(0 in the waters were measured aboard the R/V Kexue III. The mean (±SD concentration of GEM over the entire cruise was 2.61 ± 0.50 ng m−3 (range: 1.68 to 4.34 ng m−3, which were generally higher than other open oceans. The spatial distribution of GEM generally reflected a clear gradient with high levels near the coast of East China and low levels in open waters, suggesting the significant atmospheric Hg outflow from East China. The mean concentration of THg in the surface waters was 1.69 ± 0.35 ng l−1 and the RHg accounted for a considerable fraction of THg (RHg: 1.08 ± 0.28 ng l−1, %RHg/THg = 63.9%. The mean concentration of DGM in the surface waters was 63.9 ± 13.7 pg l−1 and always suggested the supersaturation of Hg(0 in the surface waters with respect to Hg(0 in the atmosphere (the degree of saturation: 7.8 ± 2.3 with a range of 3.6–14.0. The mean Hg(0 flux at the air-sea interface was estimated to be 18.3 ± 11.8 ng m−2 h−1 based on a two-layer exchange model. The high wind speed and DGM levels induced the extremely high Hg(0 emission rates. Measurements at three stations showed no clear vertical patterns of DGM, RHg and THg in the water column. Overall, the elevated Hg levels in the Yellow Sea compared with other open oceans suggested that the human activity has influenced the oceanic Hg cycle downwind of East Asia.

  4. An experimental study of formation of the mercury mixed halides HgClBr and HgBrI and of their purity

    OpenAIRE

    Rabia Ahmad; Jamshed Ali; Qamer Faisal

    2015-01-01

    Claims to have produced the mixed halides of mercury are very old. However, their stability or even their very existence was seriously questioned by Ammlung and Brill several decades back, on the basis of their study, in several solvents, of what was thought to be HgBrI. The mixed halide HgClI was already known to be unstable. On the basis of these facts, which were also lent some theoretical support, it was strongly conjectured that the mixed halides of mercury and similar elements, were...

  5. Single crystal growth, electronic structure and optical properties of Cs2HgBr4

    Science.gov (United States)

    Lavrentyev, A. A.; Gabrelian, B. V.; Vu, V. T.; Shkumat, P. N.; Parasyuk, O. V.; Fedorchuk, A. O.; Khyzhun, O. Y.

    2015-10-01

    We report on successful synthesis of high-quality single crystal of cesium mercury tetrabromide, Cs2HgBr4, by using the vertical Bridgman-Stockbarger method as well as on studies of its electronic structure. For the Cs2HgBr4 crystal, we have recorded X-ray photoelectron spectra for both pristine and Ar+ ion-bombarded surfaces. Our data indicate that the Cs2HgBr4 single crystal surface is rather sensitive with respect to Ar+ ion-bombardment. In particular, such a treatment of the Cs2HgBr4 single crystal surface alters its elemental stoichiometry. To explore peculiarities of the energy distribution of total and partial densities of states within the valence band and the conduction band of Cs2HgBr4, we have made band-structure calculations based on density functional theory (DFT) employing the augmented plane wave+local orbitals (APW+lo) method as incorporated in the WIEN2k package. The APW+lo calculations allow for concluding that the Br 4p states make the major contributions in the upper portion of the valence band, while its lower portion is dominated by contributors of the Hg 5d and Cs 5p states. Further, the main contributors to the bottom of the conduction band of Cs2HgBr4 are the unoccupied Br p and Hg s states. In addition, main optical characteristics of Cs2HgBr4 such as dispersion of the absorption coefficient, real and imaginary parts of dielectric function, electron energy-loss spectrum, refractive index, extinction coefficient and optical reflectivity have been explored from the first-principles band-structure calculations.

  6. HgCdTe barrier infrared detectors

    Science.gov (United States)

    Kopytko, M.; Rogalski, A.

    2016-05-01

    In the last decade, new strategies to achieve high-operating temperature (HOT) detectors have been proposed, including barrier structures such as nBn devices, unipolar barrier photodiodes, and multistage (cascade) infrared detectors. The ability to tune the positions of the conduction and valence band edges independently in a broken-gap type-II superlattices is especially helpful in the design of unipolar barriers. This idea has been also implemented in HgCdTe ternary material system. However, the implementation of this detector structure in HgCdTe material system is not straightforward due to the existence of a valence band discontinuity (barrier) at the absorber-barrier interface. In this paper we present status of HgCdTe barrier detectors with emphasis on technological progress in fabrication of MOCVD-grown HgCdTe barrier detectors achieved recently at the Institute of Applied Physics, Military University of Technology. Their performance is comparable with state-of-the-art of HgCdTe photodiodes. From the perspective of device fabrication their important technological advantage results from less stringent surface passivation requirements and tolerance to threading dislocations.

  7. Experimental study on Hg0 removal from flue gas over columnar MnOx-CeO2/activated coke

    International Nuclear Information System (INIS)

    Highlights: • The Hg0 removal efficiency over columnar MnCe6/activated coke up to 94%. • MnOx and CeO2 exhibited a significant synergistic role in Hg0 removal over MnCe/AC. • Lattice oxygen, chemisorbed oxygen and OH groups on the surface of MnCe/AC contributed to Hg0 oxidation. • Hg0 removal mechanisms over MnCe/AC were identified firstly. - Abstract: Mn-Ce mixed oxides supported on commercial columnar activated coke (MnCe/AC) were employed to remove elemental mercury (Hg0) at low temperatures (100–250 °C) without the assistance of HCl in flue gas. The samples were characterized by X-ray diffraction (XRD), Brunauer–Emmett–Teller (BET), X-ray photoelectron spectroscopy (XPS) and temperature programmed desorption (TPD). Effects of some factors, including Mn-Ce loading values, active component, reaction temperatures and flue gas components (O2, SO2, NO, H2O), on Hg0 removal efficiency were investigated. Results indicated that the optimal Mn-Ce loading value and reaction temperature were 6% and 190 °C, respectively. Considerable high Hg0 removal efficiency (>90%) can be obtained over MnCe6/AC under both N2/O2 atmosphere and simulated flue gas atmosphere at 190 °C. Besides, it was observed that O2 and NO exerted a promotional effect on Hg0 removal, H2O exhibited a suppressive effect, and SO2 hindered Hg0 removal seriously when in the absence of O2. Furthermore, the XPS spectra of Hg 4f and Hg-TPD results showed that the captured mercury were existed as Hg0 and HgO on the MnCe6/AC, and HgO was the major species, which illustrated that adsorption and catalytic oxidation process were included for Hg0 removal over MnCe6/AC, and catalytic oxidation played the critical role. What's more, both lattice oxygen and chemisorbed oxygen or OH groups on MnCe6/AC contributed to Hg0 oxidation. MnCe6/AC, which exhibited excellent performance on Hg0 removal in the absence of HCl, appeared to be promising in industrial application, especially for low-rank coal fired

  8. 40 CFR 60.45Da - Standard for mercury (Hg).

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 6 2010-07-01 2010-07-01 false Standard for mercury (Hg). 60.45Da... for mercury (Hg). (a) For each coal-fired electric utility steam generating unit other than an IGCC... gases that contain mercury (Hg) emissions in excess of each Hg emissions limit in paragraphs...

  9. Quasiparticle excitations in superdeformed {sup 192}Hg

    Energy Technology Data Exchange (ETDEWEB)

    Lauritsen, T.; Carpenter, M.P.; Janssens, R.V.F. [and others

    1995-08-01

    The nucleus {sup 192}Hg plays a pivotal role for superdeformation in the mass 190 region, since calculations of single-particle levels show large shell-gaps for the superdeformed (SD) shape at N = 112 and Z = 80. As a result, {sup 192}Hg is referred to as the doubly magic SD nucleus for the A = 190 region. In previous studies, only one superdeformed band was observed in this nucleus, and this fact was cited as indirect evidence that large shell gaps do indeed exist at the proposed particle numbers.

  10. Electric field gradients in Hg compounds

    DEFF Research Database (Denmark)

    Arcisauskaité, Vaida; Knecht, Stefan; Sauer, Stephan P. A.;

    2012-01-01

    We examine the performance of Density Functional Theory (DFT) approaches based on the Zeroth-Order Regular Approximation (ZORA) Hamiltonian (with and without inclusion of spinorbit coupling) for predictions of electric ¿eld gradients (EFGs) at the heavy atom Hg nucleus. This is achieved by compar......We examine the performance of Density Functional Theory (DFT) approaches based on the Zeroth-Order Regular Approximation (ZORA) Hamiltonian (with and without inclusion of spinorbit coupling) for predictions of electric ¿eld gradients (EFGs) at the heavy atom Hg nucleus. This is achieved...

  11. Synthesis and Crystal Structure of New Coordination Compound Mn2Hg4(SCN)12%新型配合物Mn2Hg4(SCN)12的合成与晶体结构分析

    Institute of Scientific and Technical Information of China (English)

    李广慧; 方奇; 薛刚; 于文涛

    2005-01-01

    A new inorganic coordination compound Mn2Hg4(SCN)12 was synthesized. The grown crystals were characterized by elemental analysis, infrared spectroscopic analysis and powder crystal X-ray diffraction in detail. The crystal structure of Mn2Hg4(SCN)12 was determined by single-crystal X-ray diffraction. It belongs to monoclinic system, P21/c space group. The cell dimensions are: a=1.171 6 nm, b=1.431 05 nm, c=2.105 1 nm,β=100.738°,and Z=4. In the structure of it, half of Mn2+ cations have five-coordinate number, and other half of Mn2+ cations have six-coordinate number; 3/4 of Hg2+ cations are coordinated by four SCN-, 1/4 of Hg2+ cations are coordinated by three SCN- and one NCS-, all the coordination geometry of Hg2+ show slightly distorted tetrahedrons. CCDC:244939.

  12. The application of 199Hg NMR and 199mHg perturbed angular correlation (PAC) spectroscopy to define the biological chemistry of HgII

    DEFF Research Database (Denmark)

    Iranzo, Olga; Thulstrup, Peter Waaben; Ryu, Seung-baek;

    2007-01-01

    H values and at peptide/HgII ratios of 3:1 with an unusual trigonal thiolate coordination mode. The resulting HgII complexes are good water-soluble models for HgII binding to the protein MerR. We have carried out a parallel study using 199Hg NMR and 199mHg perturbed angular correlation (PAC) spectroscopy...... to characterize the distinct species that are generated under different pH conditions and peptide TRI L9C/HgII ratios. These studies prove for the first time the formation of [Hg{(TRI L9C)2-(TRI L9C H)}], a dithiolate-HgII complex in the hydrophobic interior of the three-stranded coiled coil (TRI L9C)3. 199Hg NMR...... and 199mHg PAC data demonstrate that this dithiolate-HgII complex is different from the dithiolate [Hg(TRI L9C)2], and that the presence of third -helix, containing a protonated cysteine, breaks the symmetry of the coordination environment present in the complex [Hg(TRI L9C)2]. As the pH is raised...

  13. Synthesis of HgBa2Ca3Cu4O10+δ(Hg-1234) and HgBa2Ca4Cu5O12+δ(Hg-1245) from oxygen controlled precursors under high pressure

    International Nuclear Information System (INIS)

    Effects of oxygen content in the precursor have been investigated on the synthesis of HgBa2Ca4Cu5O12+δ(Hg-1245) under high pressure. The superconducting phases continuously changed from Hg-1234 to Hg-1245 with reducing the oxygen content in the precursor of Ba2Ca4Cu5O11+δ. Samples of Hg- 1245 have been synthesized by optimizing the oxygen content of the precursor with the stoichiometric composition. (author)

  14. As, Hg, and Se flue gas sampling in a coal-fired power plant and their fate during coal combustion

    Energy Technology Data Exchange (ETDEWEB)

    Jose R. Otero-Rey; Jose M. Lopez-Vilarino; Jorge Moreda-Pineiro; Elia Alonso-Rodriguez; Soledad Muniategui-Lorenzo; Purificacion Lopez-Mahia; Dario Prada-Rodriguez [University of A Coruna, A Coruna (Spain). Department of Analytical Chemistry, Faculty of Sciences

    2003-11-15

    As, Hg, and Se are the most volatile elements in the flue gas from a coal-fired power plant. Significant amounts of these elements cause an undesired direct gaseous emission, which leads to a serious environmental health risk. The main focus of this study is to evaluate the possibility of simultaneous sampling of these volatile elements using an accurate official method for Hg (the most volatile element). A study of As, Hg, and Se emissions from a 1400 MW coal-fired power plant equipped with electrostatic precipitators (ESPs) was carried out for the combustion of a mixture of two types of coal. Simultaneous sampling of coal, bottom ash, fly ash, flue gas, and particles associated with the gas phase has been performed. Flue gas has been sampled by the Ontario Hydro Method Sampling Train, an ASTM method for Hg speciation. This sampling method was tested for As and Se sampling. As and Se determinations have been performed by HG-AAS, and Hg has been determined by CV-AAS. The results were used to examine the following: overall mass balances, relative distribution of these elements in the coal-fired power plant; As, Hg, and Se concentrations in coal and combustion residues; and predominant oxidation state for Hg in flue gas. The mass balances obtained for As, Hg, and Se were satisfactory in all cases; nevertheless, relative enrichment values in fly ash for As and Se were low; therefore, we concluded that As sampling in flue gas can be conducted by application of the Ontario Hydro Method; nevertheless Se released in the gas phase is not completely collected by this sampling train. Application of this sampling method allowed for performance of Hg speciation. The results indicated that Hg(II) was the predominant species in flue gas. It has also been proved that 24%, more than 99.8%, and 90% for As, Hg, and Se in the stack emissions, respectively, were in the gaseous phase. 42 refs., 1 fig., 12 tabs.

  15. HgTe-based photodetectors in Poland

    Science.gov (United States)

    Rogalski, A.

    2009-05-01

    The purpose of this paper is to review the main achievements in the investigations of HgTe-based ternary alloys and point out the Polish contributions in development of the middle and long wavelength infrared photodetectors. Research and development efforts in Poland were concentrated mostly on uncooled market niche. At the beginning, a modified isothermal vapor phase epitaxy has been used for research and commercial fabrication of photoconductive, photoelectromagnetic, and other HgCdTe devices. Bulk growth and liquid phase epitaxy were also used. Recently, the fabrication of infrared devices relies on low temperature epitaxial technique, namely metalorganic vapor phase deposition. At present stage of development, the photoconductive and photoelectromagnetic (PEM) detectors are gradually replaced with photovoltaic devices which offer inherent advantages of no electric or magnetic bias, no heat load and no flicker noise. Potentially, photodiodes offer high performance and very fast response. However, conventional photovoltaic uncooled detectors suffer from low quantum efficiency and very low junction resistance. The problems have been solved with advanced band gap engineered architecture, multiple cell heterojunction devices connected in series, and monolithic integration of the detectors with microoptics. In final part of the paper, the Polish achievements in technology and performance of HgMnTe and HgZnTe photodetectors are presented.

  16. An experimental study of formation of the mercury mixed halides HgClBr and HgBrI and of their purity

    Directory of Open Access Journals (Sweden)

    Rabia Ahmad

    2015-06-01

    Full Text Available Claims to have produced the mixed halides of mercury are very old. However, their stability or even their very existence was seriously questioned by Ammlung and Brill several decades back, on the basis of their study, in several solvents, of what was thought to be HgBrI. The mixed halide HgClI was already known to be unstable. On the basis of these facts, which were also lent some theoretical support, it was strongly conjectured that the mixed halides of mercury and similar elements, were expected to be unstable. However, the matter does not seem to have received the attention it deserved. It was in this light that this study was taken up. What has been thought to be HgClBr has been produced by several methods and HgBrI by one or rather two methods. The product has been subjected to X-ray diffraction, FTIR and Raman studies. Studies confined to the solid product are being reported here and only those results are being presented for which all the three techniques could be employed. These studies show that a new product is indeed formed in most of these cases, but the product is not pure in any of these cases, although the impurity seems to be quite small in most of these cases. This calls for having a thorough look at not only the mixed halides of the elements, but of all compounds claimed to be like:

  17. Real-time dark-field scattering microscopic monitoring of the in situ growth of single Ag@Hg nanoalloys.

    Science.gov (United States)

    Liu, Yue; Huang, Cheng Zhi

    2013-12-23

    A comprehensive understanding of the growth mechanism of nanoalloys is beneficial in designing and synthesizing nanoalloys with precisely tailored properties to extend their applications. Herein, we present the investigation in this aspect by real-time monitoring of the in situ growth of single Ag@Hg nanoalloys, through direct amalgamation of Ag nanoparticles with elemental mercury, by dark-field scattering microscopy. Four typically shaped Ag nanoparticles, such as rods, triangular bipyramids, cubes, and spheres, were used as seeds for studying the growth of Ag@Hg nanoalloys. The scattered light of Ag nanoparticles of different shapes, on exposure to the growth solution, exhibited a noticeable blue-shift followed by a red-shift, suggesting the growth of Ag@Hg nanoalloys. The formation of Ag@Hg nanoalloys was confirmed by scanning electron microscopy, high-resolution transmit electron microscopy, X-ray diffraction, energy-dispersive X-ray spectroscopy, and elemental mapping and line scanning. Further analysis of the time-dependent spectral data and morphological change of single nanoparticles during the growth led to the visual identification of the growth mechanism of single Ag@Hg nanoalloys. Three important steps were involved: first, rapid adsorption of Hg atoms onto Ag nanoparticles; second, initial diffusion of Hg atoms into Ag nanoparticles, rounding or shortening the particles; third, further diffusion of Hg atoms leading to the formation of spherical Ag@Hg nanoalloys. On the basis of these results, Ag@Hg nanoalloys with given optical properties can be synthesized. Moreover, dark-field scattering microscopy is expected to be a powerful tool used for real-time monitoring of the in situ growth of other metal nanoparticles. PMID:24279755

  18. Heterogeneous Reduction Pathways for Hg(II) Species on Dry Aerosols: A First-Principles Computational Study.

    Science.gov (United States)

    Tacey, Sean A; Xu, Lang; Mavrikakis, Manos; Schauer, James J

    2016-04-01

    The atmospheric lifetime of mercury is greatly impacted by redox chemistry resulting from the high deposition rate of reactive mercury (Hg(II)) compared to elemental mercury (Hg(0)). Recent laboratory and field studies have observed the reduction of Hg(II), but the chemical mechanism for this reaction has not been identified. Recent experimental work has shown that the reduction reaction is heterogeneous and can occur on iron and sodium chloride aerosol surfaces. This study explores the use of density functional theory calculations to discern the reduction pathways of HgCl2, HgBr2, Hg(NO3)2, and HgSO4 on clean Fe(110), NaCl(100), and NaCl(111)(Na) surfaces. Potential energy surfaces were prepared for the various reduction pathways, indicating that the reduction pathway leading to the production of gas-phase elemental mercury is highly favorable on Fe(110) and NaCl(111)(Na). Moreover, the Fe(110) surface requires an external energy source of ∼0.5 eV to desorb the reduced mercury, whereas the NaCl(111)(Na) surface requires no energy input. The results indicate that a number of mercury species can be reduced on metallic iron and sodium chloride surfaces, which are known aerosol components, and that a photochemical reaction involving the aerosol surface is likely needed for the reaction to be catalytic. PMID:27014805

  19. Possible link between Hg and Cd accumulation in the brain of long-finned pilot whales (Globicephala melas).

    Science.gov (United States)

    Gajdosechova, Zuzana; Brownlow, Andrew; Cottin, Nicolas T; Fernandes, Mariana; Read, Fiona L; Urgast, Dagmar S; Raab, Andrea; Feldmann, Jörg; Krupp, Eva M

    2016-03-01

    The bioaccumulation of metals was investigated by analysis of liver, kidney, muscle and brain tissue of a pod of 21 long-finned pilot whales (Globicephala melas) of all ages stranded in Scotland, UK. The results are the first to report cadmium (Cd) passage through the blood-brain barrier of pilot whales and provide a comprehensive study of the long-term (up to 35 years) mammalian exposure to the environmental pollutants. Additionally, linear accumulation of mercury (Hg) was observed in all studied tissues, whereas for Cd this was only observed in the liver. Total Hg concentration above the upper neurochemical threshold was found in the sub-adult and adult brains and methylmercury (MeHg) of 2.2mg/kg was found in the brain of one individual. Inter-elemental analysis showed significant positive correlations of Hg with selenium (Se) and Cd with Se in all studied tissues. Furthermore, differences in the elemental concentrations in the liver and brain tissues were found between juvenile, sub-adult and adult groups. The highest concentrations of manganese, iron, zinc, Se, Hg and MeHg were noted in the livers, whereas Cd predominantly accumulated in the kidneys. High concentrations of Hg and Cd in the tissues of pilot whales presented in this study reflect ever increasing toxic stress on marine mammals. PMID:26748005

  20. Siderophile and chalcophile metal variations in Tertiary picrites and basalts from West Greenland with implications for the sulphide saturation history of continental flood basalt magmas

    Science.gov (United States)

    Keays, Reid R.; Lightfoot, Peter C.

    2007-04-01

    Sixty-five million year old continental flood basalts crop out on Qeqertarssuaq Island and the Nuussuaq Peninsula in West Greenland, and they include ˜1,000 m of picritic lavas and discrete 10- to 50-m-thick members of highly contaminated basalts. On Qeqertarssuaq, the lavas are allocated to the Vaîgat and Maligât Formations of which the former includes the Naujánguit member, which consists of picrites with 7-29 wt% MgO, 80-1,400 ppm Ni, 5.7-9.4 ppb Pt and 4.2-12.9 ppb Pd. The Naujánguit member contains two horizons of contaminated basalts, the Asûk and Kûgánguaq, which have elevated SiO2 (52-58 wt%) and low to moderate MgO (7.5-12.8 wt%). These lavas are broadly characterized by low Cu and Ni abundances (average, 40 ppm Ni and 45 ppm Cu) and very low Pt (0.16-0.63 ppb) and Pd (0.13-0.68 ppb) abundances, and in the case of the Asûk, they contain shale xenoliths and droplets of native iron and troilite. The contaminated basalts from Nuussuaq, the B0 to B4 members, are also usually Ni-, Cu-, and platinum-group elements (PGE)-depleted. The geochemical signatures (especially the ratios of incompatible trace elements such as Th/Nb) of all of the contaminated basalts from Qeqertarssuaq and some of those from Nuussuaq record what appears to be a chemical contribution from deltaic shales that lie immediately below the lavas. This suggests that the contamination of the magmas occurred during the migration of the magmas through plumbing systems developed in sedimentary rocks, and hence, at a high crustal level. Nickel, Cu, and PGE depletion together with geochemical signatures produced by crustal contamination are also a feature of Siberian Trap basalts from the Noril’sk region. These basalts belong to the 0- to 500-m thick, ˜5,000- to 10,000-km3 Nadezhdinsky Formation, which is centered in the Noril’sk Region. A major difference between Siberia and West Greenland is that PGE depletion in the Nadezhdinsky Formation samples with the lowest Cu and Ni contents is

  1. Quantum chemistry insight into Mg-substitution in chlorophyll by toxic heavy metals: Cd, Hg and Pb

    Science.gov (United States)

    Bechaieb, Rim; Ben Akacha, Azaiez; Gérard, Hélène

    2016-10-01

    In this paper, we examined the structural, electronic and energetic data associated to the Mg-substitution in chlorophyll by three major toxic pollutants: Cd2+, Hg2+ and Pb2+. We evidenced a highly versatile bonding of the cations with the pheophytin ligand, with a strong out-of-plane distortion for Hg and Pb. The binding energies ranged from slightly stronger than Mg2+ in the case of Hg2+ to much smaller for Pb2+. Nevertheless, our various approaches of free cations solvation allowed us to evidence that Mg-substitution should be possible for all title elements.

  2. Mercury (Hg) emissions from domestic biomass combustion for space heating.

    Science.gov (United States)

    Huang, Jiaoyan; Hopke, Philip K; Choi, Hyun-Deok; Laing, James R; Cui, Huailue; Zananski, Tiffany J; Chandrasekaran, Sriraam Ramanathan; Rattigan, Oliver V; Holsen, Thomas M

    2011-09-01

    Three mercury (Hg) species (gaseous elemental mercury (GEM), gaseous oxidized mercury (GOM), and fine particulate-bound mercury (PBM(2.5))) were measured in the stack of a small scale wood combustion chamber at 400°C, in the stack of an advanced wood boiler, and in two areas influenced by wood combustion. The low temperature process (lab-scale) emitted mostly GEM (∼99% when burning wood pellets and ∼95% when burning unprocessed wood). The high temperature wood boiler emitted a greater proportion of oxidized Hg (approximately 65%) than the low temperature system. In field measurements, mean PBM(2.5) concentrations at the rural and urban sites in winter were statistically significantly higher than in warmer seasons and were well correlated with Delta-C concentrations, a wood combustion indictor measured by an aethalometer (UV-absorbable carbon minus black carbon). Overall the results suggest that wood combustion may be an important source of oxidized mercury (mostly in the particulate phase) in northern climates in winter.

  3. Bioavailability of Cd, Zn and Hg in Soil to Nine Recombinant Luminescent Metal Sensor Bacteria

    OpenAIRE

    Olesja Bondarenko; Taisia Rõlova; Anne Kahru; Angela Ivask

    2008-01-01

    A set of nine recombinant heavy metal-specific luminescent bacterial sensors belonging to Gram-negative (Escherichia and Pseudomonas) and Gram-positive (Staphylococcus and Bacillus) genera and containing various types of recombinant metalresponse genetic elements was characterized for heavy metal bioavailability studies. All nine strains were induced by Hg and Cd and five strains also by Zn. As a lowest limit, the sensors were detecting 0.03 μg·L-1 of Hg, 2 μg·L-1 of Cd and 400 Î...

  4. Long-distance transport of Hg, Sb, and As from a mined area, conversion of Hg to methyl-Hg, and uptake of Hg by fish on the Tiber River basin, west-central Italy.

    Science.gov (United States)

    Gray, John E; Rimondi, Valentina; Costagliola, Pilario; Vaselli, Orlando; Lattanzi, Pierfranco

    2014-02-01

    Stream sediment, stream water, and fish were collected from a broad region to evaluate downstream transport and dispersion of mercury (Hg) from inactive mines in the Monte Amiata Hg District (MAMD), Tuscany, Italy. Stream sediment samples ranged in Hg concentration from 20 to 1,900 ng/g, and only 5 of the 17 collected samples exceeded the probable effect concentration for Hg of 1,060 ng/g, above which harmful effects are likely to be observed in sediment-dwelling organisms. Concentrations of methyl-Hg in Tiber River sediment varied from 0.12 to 0.52 ng/g, and although there is no established guideline for sediment methyl-Hg, these concentrations exceeded methyl-Hg in a regional baseline site (Environmental Protection Agency (USEPA) guideline recommended to protect against chronic effects to aquatic wildlife. Methyl-Hg concentrations in stream water varied from effects to aquatic wildlife (150 μg/L for As and 5.6 μg/L for Sb). Concentrations of Hg in freshwater fish muscle ranged from 0.052-0.56 μg/g (wet weight), mean of 0.17 μg/g, but only 17 % (9 of 54) exceeded the 0.30 μg/g (wet weight) USEPA fish muscle guideline recommended to protect human health. Concentrations of Hg in freshwater fish in this region generally decreased with increasing distance from the MAMD, where fish with the highest Hg concentrations were collected more proximal to the MAMD, whereas all fish collected most distal from Hg mines contained Hg below the 0.30 μg/g fish muscle guideline. Data in this study indicate some conversion of inorganic Hg to methyl-Hg and uptake of Hg in fish on the Paglia River, but less methylation of Hg and Hg uptake by freshwater fish in the larger Tiber River. PMID:23666049

  5. Chemical beam epitaxy of CdTe, HgTe, and HgCdTe

    Energy Technology Data Exchange (ETDEWEB)

    Benz, R.G. II; Wagner, B.K.; Rajavel, D.; Summers, C.J. (Physical Sciences Lab., Georgia Tech Research Inst., Atlanta, GA (USA))

    1991-05-01

    A chemical beam epitaxy (CBE) system has been implemented for the growth of CdTe, HgTe, and their alloys. The system is briefly described. Results on the cracking of the organometallic source gases are presented. Epitaxial layers have been grown from gas sources of diethylcadmium, diisopropyltelluride and Hg vapor, as well as conventional solid sources. Optical and electrical properties are reported, demonstrating the potential of CBE for growing high quality solar cell and infrared detector material. (orig.).

  6. Physical and Chemical Parameters of HgMn Stars on the Basis of the Available Data

    Science.gov (United States)

    Ghazaryan, Satenik

    2014-12-01

    For better understanding the details of physical processes affecting essentially the atmosphere of HgMn stars, I compiled the chemical abundances of nearly all the observed HgMn stars and compared them with Smith's review (1996). During this study for about 130 stars of the mentioned type, more than 65 elements' abundances were compiled and rescaled assuming solar abundances values given by Asplund (2009). This compilation results show that the heavy elements are systematically overabundant in HgMn stars (see Preston (1974) and Smith (1996)). The under abundance of HeI seems less pronounced than in Smith's review. For some elements (As, Br, Rh, Pd, Gd, Au, and U) no abundances have been shown by Smith while for the others, the results are mostly the same. Thus we arrive at a conclusion that these results are in good agreement with Smith's figure. But it is important to know that the created database is not homogenous because the HgMn stars were observed by different techniques and dissimilar methods. Consequently, the uncertainties need to be taken into account to be sure for each abundance value. It is planned also to combine the abundances of all observed A and B stars as well to be able to see the abundance stratifications changes because of the effective temperature. This work is in preparation and will be done in near future.

  7. Long-term Hg pollution induced Hg tolerance in the terrestrial isopod Porcellio scaber (Isopoda, Crustacea)

    International Nuclear Information System (INIS)

    The aim of our work was to assess the pollution-induced community tolerance (PICT) of isopod gut microbiota and pollution-induced isopod population tolerance (PIPT). Animals collected from a chronically Hg polluted and an unpolluted location were exposed for 14 days to 10 μg Hg/g dry food under laboratory conditions. The lysosomal membrane stability, hepatopancreas epithelium thickness, feeding activity and animal bacterial gut microbiota composition were determined. The results confirm the hypothesis that the response to short-term Hg exposure differs for animals from the Hg polluted and the unpolluted field locations. The animals and their gut microbiota from the Hg polluted location were less affected by Hg in a short-term feeding experiment than those from the unpolluted environment. We discuss the pollution-induced population tolerance of isopods and their gut microbiota as a measure of effects of long-term environmental pollution. The ecological consequences of such phenomena are also discussed. - Isopods (Porcellio scaber) as well as their bacterial gut community from a mercury-polluted site are mercury tolerant

  8. Long-term Hg pollution induced Hg tolerance in the terrestrial isopod Porcellio scaber (Isopoda, Crustacea)

    Energy Technology Data Exchange (ETDEWEB)

    Lapanje, A. [University of Ljubljana, Biotechnical Faculty, Department of Biology, Vecna pot 111, 1000 Ljubljana (Slovenia); Institute of Physical Biology, Veliko Mlacevo 59, 1290 Grosuplje (Slovenia)], E-mail: ales.lapanje@bf.uni-lj.si; Drobne, D. [University of Ljubljana, Biotechnical Faculty, Department of Biology, Vecna pot 111, 1000 Ljubljana (Slovenia); Nolde, N. [Institute Jozef Stefan, Department of Environmental Sciences, Jamova 39, 1000 Ljubljana (Slovenia); Valant, J. [University of Ljubljana, Biotechnical Faculty, Department of Biology, Vecna pot 111, 1000 Ljubljana (Slovenia); Muscet, B. [Institute of Physical Biology, Veliko Mlacevo 59, 1290 Grosuplje (Slovenia); Leser, V. [University of Ljubljana, Biotechnical Faculty, Department of Biology, Vecna pot 111, 1000 Ljubljana (Slovenia); Rupnik, M. [Institute of Public Health, Prvomajska 1, 2000 Maribor (Slovenia); Faculty of Medicine, University of Maribor, Slomskov trg 15, 2000 Maribor (Slovenia)

    2008-06-15

    The aim of our work was to assess the pollution-induced community tolerance (PICT) of isopod gut microbiota and pollution-induced isopod population tolerance (PIPT). Animals collected from a chronically Hg polluted and an unpolluted location were exposed for 14 days to 10 {mu}g Hg/g dry food under laboratory conditions. The lysosomal membrane stability, hepatopancreas epithelium thickness, feeding activity and animal bacterial gut microbiota composition were determined. The results confirm the hypothesis that the response to short-term Hg exposure differs for animals from the Hg polluted and the unpolluted field locations. The animals and their gut microbiota from the Hg polluted location were less affected by Hg in a short-term feeding experiment than those from the unpolluted environment. We discuss the pollution-induced population tolerance of isopods and their gut microbiota as a measure of effects of long-term environmental pollution. The ecological consequences of such phenomena are also discussed. - Isopods (Porcellio scaber) as well as their bacterial gut community from a mercury-polluted site are mercury tolerant.

  9. Hg/HgO electrode and hydrogen evolution potentials in aqueous sodium hydroxide

    Energy Technology Data Exchange (ETDEWEB)

    Nickell, Ryan A.; Zhu, Wenhua H.; Payne, Robert U.; Cahela, Donald R.; Tatarchuk, Bruce J. [Center for Microfibrous Materials Manufacturing, Department of Chemical Engineering, 230 Ross Hall, Auburn University, Auburn, AL 36849 (United States)

    2006-10-27

    The Hg/HgO electrode is usually utilized as a reference electrode in alkaline solution such as for development of an alkaline hydrogen electrode. The reference electrode provides a suitable reference point but is available from few commercial vendors and suffers from inadequate documentation on potential in varying electrolytes. A new numerical method uses activity, activity coefficients, and a few correlated empirical equations to determine the potential values in both dilute and concentrated sodium hydroxide solutions at temperatures of 0-90{sup o}C and at concentrations of 0.100-12.8mol kg{sub H{sub 2}O}{sup -1}. The computed potentials of the Hg/HgO electrodes versus a normal hydrogen electrode (NHE) at 25{sup o}C and 1atm are 0.1634V for 0.100m, 0.1077V for 1.00m, and 0.0976V for 1.45m NaOH solutions. The Hg/HgO reduction potential further changes to -0.0751V versus NHE and hydrogen evolution potential changes to -0.9916V versus NHE in a solution of 30.0wt.% NaOH at 80{sup o}C. The calculated values are compared with the measured data at 25 and 75{sup o}C. The experimental data agree well with the numerical values computed from the theoretical and empirical equations. (author)

  10. Hg/HgO electrode and hydrogen evolution potentials in aqueous sodium hydroxide

    Science.gov (United States)

    Nickell, Ryan A.; Zhu, Wenhua H.; Payne, Robert U.; Cahela, Donald R.; Tatarchuk, Bruce J.

    The Hg/HgO electrode is usually utilized as a reference electrode in alkaline solution such as for development of an alkaline hydrogen electrode. The reference electrode provides a suitable reference point but is available from few commercial vendors and suffers from inadequate documentation on potential in varying electrolytes. A new numerical method uses activity, activity coefficients, and a few correlated empirical equations to determine the potential values in both dilute and concentrated sodium hydroxide solutions at temperatures of 0-90 °C and at concentrations of 0.100-12.8 mol k gH2O-1 . The computed potentials of the Hg/HgO electrodes versus a normal hydrogen electrode (NHE) at 25 °C and 1 atm are 0.1634 V for 0.100m, 0.1077 V for 1.00m, and 0.0976 V for 1.45m NaOH solutions. The Hg/HgO reduction potential further changes to -0.0751 V versus NHE and hydrogen evolution potential changes to -0.9916 V versus NHE in a solution of 30.0 wt.% NaOH at 80 °C. The calculated values are compared with the measured data at 25 and 75 °C. The experimental data agree well with the numerical values computed from the theoretical and empirical equations.

  11. Carbon and other light element contents in the Earth's core based on first-principles molecular dynamics.

    Science.gov (United States)

    Zhang, Yigang; Yin, Qing-Zhu

    2012-11-27

    Carbon (C) is one of the candidate light elements proposed to account for the density deficit of the Earth's core. In addition, C significantly affects siderophile and chalcophile element partitioning between metal and silicate and thus the distribution of these elements in the Earth's core and mantle. Derivation of the accretion and core-mantle segregation history of the Earth requires, therefore, an accurate knowledge of the C abundance in the Earth's core. Previous estimates of the C content of the core differ by a factor of ∼20 due to differences in assumptions and methods, and because the metal-silicate partition coefficient of C was previously unknown. Here we use two-phase first-principles molecular dynamics to derive this partition coefficient of C between liquid iron and silicate melt. We calculate a value of 9 ± 3 at 3,200 K and 40 GPa. Using this partition coefficient and the most recent estimates of bulk Earth or mantle C contents, we infer that the Earth's core contains 0.1-0.7 wt% of C. Carbon thus plays a moderate role in the density deficit of the core and in the distribution of siderophile and chalcophile elements during core-mantle segregation processes. The partition coefficients of nitrogen (N), hydrogen, helium, phosphorus, magnesium, oxygen, and silicon are also inferred and found to be in close agreement with experiments and other geochemical constraints. Contents of these elements in the core derived from applying these partition coefficients match those derived by using the cosmochemical volatility curve and geochemical mass balance arguments. N is an exception, indicating its retention in a mantle phase instead of in the core. PMID:23150591

  12. A physiological role for HgII during phototrophic growth

    Science.gov (United States)

    Grégoire, D. S.; Poulain, A. J.

    2016-02-01

    The bioaccumulation of toxic monomethylmercury is influenced by the redox reactions that determine the amount of mercury (Hg) substrate--HgII or Hg0 (refs ,)--that is available for methylation. Phototrophic microorganisms can reduce HgII to Hg0 (ref. ). This reduction has been linked to a mixotrophic lifestyle, in which microbes gain energy photosynthetically but acquire diverse carbon compounds for biosynthesis from the environment. Photomixotrophs must maintain redox homeostasis to disperse excess reducing power due to the accumulation of reduced enzyme cofactors. Here we report laboratory experiments in which we exposed purple bacteria growing in a bioreactor to HgII and monitored Hg0 concentrations. We show that phototrophs use HgII as an electron sink to maintain redox homeostasis. Hg0 concentrations increased only when bacteria grew phototrophically, and when bacterial enzyme cofactor ratios indicated the presence of an intracellular redox imbalance. Under such conditions, bacterial growth rates increased with increasing HgII concentrations; when alternative electron sinks were added, Hg0 production decreased. We conclude that Hg can fulfil a physiological function in bacteria, and that photomixotrophs can modify the availability of Hg to methylation sites.

  13. Hg Vetical Transference in Soil—Water System

    Institute of Scientific and Technical Information of China (English)

    GUOYIJUN; MOUSUSEN; 等

    1998-01-01

    Hg vertial transference in soil-water system was studied by analyzing Hg vertical ditribution in soil column after adding Hg and one of the two leacheates,deionzied water or acid rain,into soil column.The results indicated that Hg was hardly transferable in puple soil.About 86%-88% of the total soil Hg was distributed in the top layer (0-2cm) and to Hg was detected in the leakage when the purple soil column was leached by deionized water and simulated acid rain.But Hg was more movalbe in yellow soil with only about 20%-22% of the total soil Hg distributed in the top layer (0-2cm),and about 17%-25% washed out from the soil column by deionized water and simulted acid rain,Incremant in soil bulk density colud reduce Hg leaching,thus the more the Hg kept in soil,the less the Hg leached into underground water,Deionized water and acid rain almost played the same role in leaching Hg.Bentioint was most effecient in preventing Hg from vertcal transferring in the soil coulumn.

  14. Statistical analysis from recent abundance determinations in HgMn stars

    Science.gov (United States)

    Ghazaryan, S.; Alecian, G.

    2016-08-01

    To better understand the hot chemically peculiar group of HgMn stars, we have considered a compilation of a large number of recently published data obtained for these stars from spectroscopy. We compare these data to the previous compilation by Smith. We confirm the main trends of the abundance peculiarities, namely the increasing overabundances with increasing atomic number of heavy elements, and their large spread from star to star. For all the measured elements, we have looked for correlations between abundances and effective temperature (Teff). In addition to the known correlation for Mn, some other elements are found to show some connection between their abundances and Teff. We have also checked if multiplicity is a determinant parameter for abundance peculiarities determined for these stars. A statistical analysis using a Kolmogorov-Smirnov test shows that the abundances anomalies in the atmosphere of HgMn stars do not present significant dependence on the multiplicity.

  15. MBE HgCdTe heterostructure detectors

    Science.gov (United States)

    Schulman, Joel N.; Wu, Owen K.

    1990-01-01

    HgCdTe has been the mainstay for medium (3 to 5 micron) and long (10 to 14 micron) wavelength infrared detectors in recent years. Conventional growth and processing techniques are continuing to improve the material. However, the additional ability to tailor composition and placement of doped layers on the tens of angstroms scale using molecular beam epitaxy (MBE) provides the opportunity for new device physics and concepts to be utilized. MBE-based device structures to be discussed here can be grouped into two categories: tailored conventional structures and quantum structures. The tailored conventional structures are improvements on familiar devices, but make use of the ability to create layers of varying composition, and thus band gap, at will. The heterostructure junction can be positioned independently of doping p-n junctions. This allows the small band gap region in which the absorption occurs to be separated from a larger band gap region in which the electric field is large and where unwanted tunneling can occur. Data from hybrid MBE/liquid phase epitaxy (LPE)/bulk structures are given. Quantum structures include the HgTe-CdTe superlattice, in which the band gap and transport can be controlled by alternating thin layers (tens of angstroms thick) of HgTe and CdTe. The superlattice has been shown to exhibit behavior which is non-alloy like, including very high hole mobilities, two-dimensional structure in the absorption coefficient, resonant tunneling, and anisotropic transport.

  16. Thermally switchable dispersions of thermochromic Ag2HgI4 nanoparticles.

    Science.gov (United States)

    Schwiertz, Janine; Geist, André; Epple, Matthias

    2009-04-28

    Thermochromic Ag(2)HgI(4) nanoparticles were prepared by rapid precipitation from aqueous solution. Stable colloids were formed by coating the particles with four different polymers, respectively. The four resulting systems of functionalised Ag(2)HgI(4) nanoparticles were characterised with respect to their polymer content (elemental analysis), particle size (dynamic light scattering, scanning electron microscopy), optical properties in dispersion (UV spectroscopy), crystallinity (X-ray powder diffraction), and thermochromic transition temperature (differential scanning calorimetry) and also compared to the unfunctionalised bulk phase Ag(2)HgI(4). Stable dispersions with a reversible temperature-induced colour change from yellow to orange (T(trs) = 25-40 degrees C) were obtained. PMID:19352519

  17. Efficient removal and highly selective adsorption of Hg2+ by polydopamine nanospheres with total recycle capacity

    International Nuclear Information System (INIS)

    Highlights: • The PDA nanospheres with uniform diameter of 150–200 nm were used to remove Hg2+ efficiently and selectively. • The desorption capacity of PDA nanospheres was 100% in pH 1. • The structure and removal capacity of PDA nanospheres remained almost unchanged after recycling five times. - Abstract: This study reported a new method for efficient removal of Hg2+ from contaminated water using highly selective adsorptive polydopamine (PDA) nanospheres, which were uniform and had a small diameter (150–200 nm). The adsorption isotherms, kinetics, thermodynamics were investigated. Also, the effects of ionic strength, co-existing ions on removing ability of PDA nanospheres for Hg2+ were studied. Adsorption of Hg2+ was very fast and efficient as adsorption equilibrium was completed within 4 h and the maximum adsorption capacities were 1861.72 mg/g, 2037.22 mg/g, and 2076.81 mg/g at 298 K, 313 K, and 328 K respectively, increasing with increasing of temperature. The PDA nanospheres exhibited highly selective adsorption of Hg2+ and had a total desorption capacity of 100% in hydrochloric acid solution, pH 1. The results showed that the structure of PDA nanospheres remained almost unchanged after recycling five times. Furthermore, X-ray photoelectron spectroscopy (XPS) was employed to determine the elements of PDA nanospheres before and after Hg2+ adsorption. Considering their efficient and highly Hg2+ selective adsorption, total recycle capacity, and high stability, PDA nanospheres will be feasible in a number of practical applications

  18. Bioavailability of Cd, Zn and Hg in Soil to Nine Recombinant Luminescent Metal Sensor Bacteria

    Directory of Open Access Journals (Sweden)

    Olesja Bondarenko

    2008-11-01

    Full Text Available A set of nine recombinant heavy metal-specific luminescent bacterial sensors belonging to Gram-negative (Escherichia and Pseudomonas and Gram-positive (Staphylococcus and Bacillus genera and containing various types of recombinant metalresponse genetic elements was characterized for heavy metal bioavailability studies. All nine strains were induced by Hg and Cd and five strains also by Zn. As a lowest limit, the sensors were detecting 0.03 μg·L-1 of Hg, 2 μg·L-1 of Cd and 400 μg·L-1 of Zn. Limit of determination of the sensors depended mostly on metal-response element, whereas the toxicity of those metals towards the sensor bacteria was mostly dependent on the type of the host bacterium, with Gram-positive strains being more sensitive than Gram-negative ones. The set of sensors was used to evaluate bioavailability of Hg, Cd and Zn in spiked soils. The bioavailable fraction of Cd and Zn in soil suspension assay (2.6 – 5.1% and 0.32 – 0.61%, of the total Cd and Zn, respectively was almost comparable for all the sensors, whereas the bioavailability of Hg was about 10-fold higher for Gram-negative sensor cells (30.5% of total Hg, compared to Gram-positive ones (3.2% of the total Hg. For Zn, the bioavailable fraction in soil-water suspensions and respective extracts was comparable (0.37 versus 0.33% of the total Zn. However, in the case of Cd, for all the sensors used and for Hg concerning only Gram-negative sensor strains, the bioavailable fraction in soilwater suspensions exceeded the water-extracted fraction about 14-fold, indicating that upon direct contact, an additional fraction of Cd and Hg was mobilized by those sensor bacteria. Thus, for robust bioavailability studies of heavy metals in soils any type of genetic metal-response elements could be used for the construction of the sensor strains. However, Gram-positive and Gram-negative senor strains should be used in

  19. Fractionation distribution and preliminary ecological risk assessment of As, Hg and Cd in ornithogenic sediments from the Ross Sea region, East Antarctica.

    Science.gov (United States)

    Lou, Chuangneng; Liu, Xiaodong; Nie, Yaguang; Emslie, Steven D

    2015-12-15

    To evaluate mobility of toxic elements and their potential ecological risk caused by seabird biovectors, the fractionation distributions of arsenic (As), mercury (Hg) and cadmium (Cd) were investigated in three ornithogenic sediment profiles from the Ross Sea region, East Antarctica. The results show residual As holds a dominant position, and Hg mainly derives from residual, organic matter-bound and humic acid-bound fractions, indicating weak mobility of As and Hg. However, exchangeable Cd occupies a considerable proportion in studied samples, suggesting Cd has strong mobility. The preliminary evaluation of Sediment Quality Guidelines (SGQs) shows adverse biological effects may occur occasionally for As and Cd, and rarely for Hg. Using Risk Assessment Code (RAC), the ecological risk is assessed at moderate, low and very high for As, Hg and Cd pollution, respectively. Organic matter derived from guano is the main factor controlling the mobility of Hg and Cd through adsorption and complexation.

  20. Isotopic Composition of Gaseous Elemental Mercury in the Free Troposphere of the Pic du Midi Observatory, France.

    Science.gov (United States)

    Fu, Xuewu; Marusczak, Nicolas; Wang, Xun; Gheusi, François; Sonke, Jeroen E

    2016-06-01

    Understanding the sources and transformations of mercury (Hg) in the free troposphere is a critical aspect of global Hg research. Here we present one year of observations of atmospheric Hg speciation and gaseous elemental Hg (GEM) isotopic composition at the high-altitude Pic du Midi Observatory (2860 m above sea level) in France. Biweekly integrated GEM from February 2012 to January 2013 revealed significant variations in δ(202)HgGEM (-0.04‰ to 0.52‰) but not in Δ(199)HgGEM (-0.17‰ to -0.27‰) or Δ(200)HgGEM (-0.10‰ to 0.05‰). δ(202)HgGEM was negatively correlated with CO and reflected air mass origins from Europe (high CO, low δ(202)HgGEM) and from the Atlantic Ocean (low CO, high δ(202)HgGEM). We suggest that the δ(202)HgGEM variations represent mixing of recent low δ(202)HgGEM European anthropogenic emissions with high δ(202)HgGEM northern hemispheric background GEM. In addition, Atlantic Ocean free troposphere air masses showed a positive correlation between δ(202)HgGEM and gaseous oxidized Hg (GOM) concentrations, indicative of mass-dependent Hg isotope fractionation during GEM oxidation. On the basis of atmospheric δ(202)HgGEM and speciated Hg observations, we suggest that the oceanic free troposphere is a reservoir within which GEM is readily oxidized to GOM. PMID:27214126

  1. First Observations of Laser-Excited Hg3 and Hg2RG Spectra in a Supersonic Expansion Beam

    Science.gov (United States)

    Koperski; Atkinson; Krause

    1998-02-01

    Triatomic van der Waals complexes of mercury have been observed in a supersonic expansion beam crossed with a laser beam to produce excitation and fluorescence spectra. The expansion beam consisting of mercury and a (noble) carrier gas (RG) was excited in three separate spectral regions: in the vicinity of the Hg 2537 A intercombination line, near the (forbidden) Hg 6(3)P2 <-- 6(1)S0 atomic transition (2200-2290 A), and in the region of the Hg2 G0(+)u <-- X0(+)g transition (1975-2080 A). The resulting spectra, which were recorded in the spectral range 1900-6000 A, contained, in addition to the known Hg, Hg2, and HgRG components, new absorption and fluorescence bands that are ascribed to Hg2RG and Hg3 complexes. Copyright 1998 Academic Press. Copyright 1998Academic Press PMID:9473437

  2. On the valence state of Hg in (Hg, Cr)Sr2CuO4+δ superconductor

    International Nuclear Information System (INIS)

    The 1201-type of superconducting samples of nominal composition (Hg0.7Cr0.3)Sr2CuO4+δ, were synthesised in partial vacuum and subsequently annealed in oxygen and argon. The Tc onset for the different samples is found to be ∼58 K. Hg LIII-edge measurements have clearly shows that Hg is in divalent state in all the (Hg,Cr)-1201 samples. (author)

  3. Exposures of dental professionals to elemental mercury and methylmercury.

    Science.gov (United States)

    Goodrich, Jaclyn M; Chou, Hwai-Nan; Gruninger, Stephen E; Franzblau, Alfred; Basu, Niladri

    2016-01-01

    Mercury (Hg) exposure, a worldwide public health concern, predominantly takes two forms--methylmercury from fish consumption and elemental Hg from dental amalgam restorations. We recruited 630 dental professionals from an American Dental Association meeting to assess Hg body burden and primary sources of exposure in a dually exposed population. Participants described occupational practices and fish consumption patterns via questionnaire. Hg levels in biomarkers of elemental Hg (urine) and methylmercury (hair and blood) were measured with a Direct Mercury Analyzer-80 and were higher than the general US population. Geometric means (95% CI) were 1.28 (1.19-1.37) μg/l in urine, 0.60 (0.54-0.67) μg/g in hair and 3.67 (3.38-3.98) μg/l in blood. In multivariable linear regression, personal amalgams predicted urine Hg levels along with total years in dentistry, amalgams handled, working hours and sex. Fish consumption patterns predicted hair and blood Hg levels, which were higher among Asians compared with Caucasians. Five species contributed the majority of the estimated Hg intake from fish--swordfish, fresh tuna, white canned tuna, whitefish and king mackerel. When studying populations with occupational exposure to Hg, it is important to assess environmental exposures to both elemental Hg and methylmercury as these constitute a large proportion of total exposure. PMID:26329138

  4. Study of Hg vacancies in (Hg,Cd)Te after THM growth and post-growth annealing by positron annihilation

    OpenAIRE

    Krause, R.; Klimakow, A.; Kießling, F. M.; Polity, A.; Gille, Peter; Schenk, M.

    1990-01-01

    Positron lifetime measurements have been performed to study vacancy defects in Hg0.78Cd0.22Te. Post-growth annealing under various Hg vapour pressure conditions have been used to create a well-defined number of Hg vacancies. The sensitivity range of the positron annihilation method was found to be 1015 < cHgvac

  5. RESPONSES OF MEMBRANE PROTECTION ENZYME SYSTEM OF TOBACCO LEAVES ON Hg, Cd AND Pb STRESSES IN SOIL%烟草叶片膜保护酶系统对土壤Hg,Cd,Pb胁迫的响应

    Institute of Scientific and Technical Information of China (English)

    严重玲; 林鹏; 王晓蓉

    2002-01-01

    采用盆栽实验,就烟草膜保护酶系统对土壤Hg,Cd,Pb胁迫的响应进行研究.结果表明:随着Hg,Cd,Pb浓度的增加,POD活性逐渐增加,CAT活性逐渐减小,SOD活性在三种元素共同作用时逐渐下降,在元素单一或两两作用时,SOD活性呈单峰曲线,但总体水平仍较低.土壤Hg,Cd,Pb的这种影响表现出三元素共同作用>两两元素作用>单一元素作用.影响的结果造成活性氧产生与清除之间的不平衡,致使相关生理生化过程紊乱.三种重金属对烟草活性氧清除系统的影响表现出明显地协同作用.%Pot experiment was used to study the responses of membrane protection enzyme system of tobac-co loves on Hg, Cd and Pb stresses in soil. The results showed that POD activity gradually increased with in-creasing concetrations of Hg, Cd and Pb. CAT and SOD activity gradually decreased under three heavy metalscommon existing and SOD variation curve showed unimodal curve under single or two elements existing withincrease of concentration of Hg, Cd and Pb. The effects of Hg, Cd and Pb in soil: three elemets together>twoelements together>single element only. The effects resulted in an imbalance -- activated oxygen produce andscavenge and physiological biochemical process disorder. There was a synergistic action for the effect of Hg, Cdand Pb in soil on membrane protection enzyme system in tobacco leaves.

  6. Development of Se and Hg determination methods in woman's hair

    International Nuclear Information System (INIS)

    INAA method of mercury (Hg) and selenium (Se) determination was carried out by using comparison factor of 75Se peak at 264.4 keV and 279.2 keV using Ge (Li) detector EG and G Ortec and 8100 MCA Canberra. The average of the factor was 2,35. The samples were pregnane women's hair from DIY. The direction of this investigation was to find data for further monitoring of contamination and the health of baby will be born. DIY was chosen because not much of industries and DIY is not fishing region. It is known that many kind of industries product Hg contaminant, and fish usually contain high concentration of Hg. The results are: 1. Hg concentration was 0,32 - 5,20 ppm and the Se = 0,43 - 6,08 ppm. Hg can be detected in all of the samples, and only in one sample that Se can not be find. 2. Fish consumer : Hg = 0,32 - 5,2 ppm and Se = 0 - 194 ppm. The controls : Hg = 0,32 - 2,03 ppm and Se 0,57 - 6,08 ppm. 3. Employer : Hg 0,52 - 5,04 ppm and Se = 0,59 - 1,94 ppm. Control : Hg = 0,32 - 5,20 ppm and Se = 0,43 - 2,94 ppm. It can be concluded that: I. comparison factor is 2,35. The factor can be used for Hg calculation with 7,6 % accuracy for Hg and 3,31 % for se. This results of the Hg and se concentration can be used for the further contamination and health monitoring. Most of the se/Hg comparison were 1 : 1. It means the se concentration was similar with the Hg. (author)

  7. Allyl- iso-propyltelluride, a new MOVPE precursor for CdTe, HgTe and (Hg,Cd)Te

    Science.gov (United States)

    Hails, Janet E.; Cole-Hamilton, David J.; Stevenson, John; Bell, William

    2000-06-01

    The use of allyl- iso-propyltelluride as the tellurium precursor for the growth of CdTe, HgTe and (Hg,Cd)Te by metal organic vapour-phase epitaxy has been investigated. It has proved to be an efficient source of tellurium with growth rates for HgTe and (Hg,Cd)Te of up to 10 μm h -1 at 300°C. The best CdTe was grown at 4.5 μm h -1 under Me 2Cd-rich conditions at 300°C in the presence of Hg vapour.

  8. Exploiting the higher specificity of silver amalgamation: selective detection of mercury(II) by forming Ag/Hg amalgam.

    Science.gov (United States)

    Deng, Li; Ouyang, Xiangyuan; Jin, Jianyu; Ma, Cheng; Jiang, Ying; Zheng, Jing; Li, Jishan; Li, Yinhui; Tan, Weihong; Yang, Ronghua

    2013-09-17

    Heavy metal ion pollution poses severe risks in human health and the environment. Driven by the need to detect trace amounts of mercury, this article demonstrates, for the first time, that silver/mercury amalgamation, combining with DNA-protected silver nanoparticles (AgNPs), can be used for rapid, easy and reliable screening of Hg(2+) ions with high sensitivity and selectivity over competing analytes. In our proposed approach, Hg(2+) detection is achieved by reducing the mercury species to elemental mercury, silver atoms were chosen as the mercury atoms' acceptors by forming Ag/Hg amalgam. To signal fluorescently this silver amalgamation event, a FAM-labeled ssDNA was employed as the signal reporter. AgNPs were grown on the DNA strand that resulted in greatly quenching the FAM fluorescence. Formation of Ag/Hg amalgam suppresses AgNPs growth on the DNA, leading to fluorescence signal increase relative to the fluorescence without Hg(2+) ions, as well as marked by fluorescence quenching. This FAM fluorescence enhancement can be used for detection of Hg(2+) at the a few nanomolar level. Moreover, due to excellent specificity of silver amalgamation with mercury, the sensing system is highly selective for Hg(2+) and does not respond to other metal ions with up to millimolar concentration levels. This sensor is successfully applied to determination of Hg(2+) in tap water, spring water and river water samples. The results shown herein have important implications in the development of new fluorescent sensors for the fast, easy, and selective detection and quantification of Hg(2+) in environmental and biological samples. PMID:23937672

  9. Phase equilibria and thermodynamic functions for Ag–Hg and Cu–Hg binary systems

    International Nuclear Information System (INIS)

    Highlights: ► The thermodynamic properties of Ag–Hg and Cu–Hg are explored in order to facilitate dental materials design. ► A self-consistent set of thermodynamic parameters is obtained. ► The experimental information can be well reproduced by the optimized thermodynamic data. - Abstract: In order to facilitate the computational design of new amalgams for novel dental alloys, the phase equilibria, phase diagrams and thermodynamic functions for Ag–Hg and Cu–Hg binary systems are explored in this work, based on the CALPHAD framework and experimental characterizations. The Gibbs free energies of the solution phases as well as the stoichiometric phases are calculated, with the aid of enthalpies of mixing, activities, enthalpies of formation, and phase equilibrium data. The thermodynamic descriptions provided in this work enable the stabilities of each phase at various temperatures and compositions to be well described, which contribute to the establishment of a general database to design novel metallic dental materials.

  10. Heavy metal tolerance (Cr, Ag and Hg in bacteria isolated from sewage

    Directory of Open Access Journals (Sweden)

    Agostinho A. de Lima e Silva

    2012-12-01

    Full Text Available Samples of sewage from a university hospital and a chemistry technical school were analysed for the percentage of bacterial tolerance to chromium (Cr, silver (Ag and mercury (Hg. Additionally, we investigated the effect of these metals on pigmentation and on some enzymatic activities of the metal tolerant strains isolated, as well as antimicrobial resistance in some metal tolerant Enterobacteriaceae strains. Tolerance to Cr was observed mainly in Gram positive bacteria while in the case of Ag and Hg the tolerant bacteria were predominately Gram negative. Hg was the metal for which the percentage of tolerance was significantly higher, especially in samples from the hospital sewage (4.1%. Mercury also had the most discernible effect on color of the colonies. Considering the effect of metals on the respiratory enzymes, one strain of Ag-tolerantBacillus sp. and one of Hg-tolerant P. aeruginosa were unable to produce oxidase in the presence of Ag and Hg, respectively, while the expression of gelatinase was largely inhibited in various Gram negative strains (66% by Cr. Drug resistance in Hg-tolerant Enterobacteriaceae strains isolated from the university hospital sewage was greater than 80%, with prevalence of multiple resistance, while the Ag-tolerant strains from the same source showed about 34% of resistance, with the predominance of mono-resistance. Our results showed that, despite the ability of metal tolerant strains to survive and grow in the presence of these elements, the interactions with these metals may result in metabolic or phisiological changes in this group of bacteria.

  11. Heavy metal tolerance (Cr, Ag AND Hg) in bacteria isolated from sewage.

    Science.gov (United States)

    Lima de Silva, Agostinho A; de Carvalho, Márcia A Ribeiro; de Souza, Sérgio A L; Dias, Patrícia M Teixeira; da Silva Filho, Renato G; de Meirelles Saramago, Carmen S; de Melo Bento, Cleonice A; Hofer, Ernesto

    2012-10-01

    Samples of sewage from a university hospital and a chemistry technical school were analysed for the percentage of bacterial tolerance to chromium (Cr), silver (Ag) and mercury (Hg). Additionally, we investigated the effect of these metals on pigmentation and on some enzymatic activities of the metal tolerant strains isolated, as well as antimicrobial resistance in some metal tolerant Enterobacteriaceae strains. Tolerance to Cr was observed mainly in Gram positive bacteria while in the case of Ag and Hg the tolerant bacteria were predominately Gram negative. Hg was the metal for which the percentage of tolerance was significantly higher, especially in samples from the hospital sewage (4.1%). Mercury also had the most discernible effect on color of the colonies. Considering the effect of metals on the respiratory enzymes, one strain of Ag-tolerant Bacillus sp. and one of Hg-tolerant P. aeruginosa were unable to produce oxidase in the presence of Ag and Hg, respectively, while the expression of gelatinase was largely inhibited in various Gram negative strains (66% by Cr). Drug resistance in Hg-tolerant Enterobacteriaceae strains isolated from the university hospital sewage was greater than 80%, with prevalence of multiple resistance, while the Ag-tolerant strains from the same source showed about 34% of resistance, with the predominance of mono-resistance. Our results showed that, despite the ability of metal tolerant strains to survive and grow in the presence of these elements, the interactions with these metals may result in metabolic or phisiological changes in this group of bacteria.

  12. Analysis of As, Cr and Hg in crude oil sludge by using instrumental neutron activation analysis (INAA)

    International Nuclear Information System (INIS)

    Environment are carrying toxic elements. The aim of this study was to determine As, Cr and Hg elements in crude oil sludge. In this study, crude oil sludge samples from a refining plant at Kerteh, Terengganu was carried out using Instrumental Neutron Activation Analysis (INAA). The samples were packed and irradiated at the Malaysian Nuclear Agency reactor TRIGA Mark II. Later, the samples were counted using a HPGe detector and were analyzed using the SAMPO 90 software. The certified reference material (CRM) namely NBS Coal Fly Ash 1633a was used as a standard to obtain the concentration average using a comparative method. A total of 11 elements (i.e. As, Co, Cr, Fe, Ga, Hg, Mn, Na, Sc, Se and Sr) were determined in all samples. The concentrations of As, Cr and Hg were found to be in the range of 0-18.8, 98.2-124 and 52.8-57.9 μg.g-1 respectively. From the concentration of these elements, the results showed that the value for total As element is low but the values for the total Cr and Hg are considerable higher than the permissible value. However, almost all the potential environmental impacts can be controlled by sludge disposal options such as well-designed, carefully, efficiently and continuously managed, by following accepted guidelines and regulations. (Author)

  13. Source attribution and process analysis for atmospheric mercury in East China simulated by CMAQ-Hg

    OpenAIRE

    Zhu, J.; Wang, T.; J. Bieser; V. Matthias

    2015-01-01

    The contribution from different emission sources and atmospheric processes to gaseous elemental mercury (GEM), gaseous oxidized mercury (GOM), particulate bound mercury (PBM) and mercury deposition in East China were quantified using the Community Multi-scale Air Quality (CMAQ-Hg) modeling system run with nested grid resolution of 27 km. Natural source (NAT) and six categories of anthropogenic mercury sources (ANTH) including cement production (CEM), domestic life (DOM), indus...

  14. Source attribution and process analysis for atmospheric mercury in eastern China simulated by CMAQ-Hg

    OpenAIRE

    Zhu, J.; Wang, T.; J. Bieser; V. Matthias

    2015-01-01

    The contribution from different emission sources and atmospheric processes to gaseous elemental mercury (GEM), gaseous oxidized mercury (GOM), particulate bound mercury (PBM) and mercury deposition in eastern China were quantified using the Community Multi-scale Air Quality (CMAQ-Hg) modeling system run with a nested domain. Natural sources (NAT) and six categories of anthropogenic mercury sources (ANTH) including cement production (CEM), domestic life (DOM), industrial boil...

  15. Design of a ROIC for scanning type HgCdTe LWIR focal plane arrays

    OpenAIRE

    Yazıcı, Melik; Yazici, Melik; Kayahan, Hüseyin; Kayahan, Huseyin; Ceylan, Ömer; Ceylan, Omer; Gürbüz, Yaşar; Gurbuz, Yasar

    2010-01-01

    Design of a silicon readout integrated circuit (ROIC) for LWIR HgCdTe Focal Plane is presented. ROIC incorporates time delay integration (TDI) functionality over seven elements with a supersampling rate of three, increasing SNR and the spatial resolution. Novelty of this topology is inside TDI stage; integration of charges in TDI stage implemented in current domain by using switched current structures that reduces required area for chip and improves linearity performance. ROIC, in terms of...

  16. Novel M(II)-Hg(II) coordination polymers generated from metal-containing building blocks M(2-pyrazinecarboxylate) 2 · (H 2O) 2 (M=Cu, Ni, Co) and HgCl 2

    Science.gov (United States)

    Dong, Yu-Bin; Smith, Mark D.; zur Loye, Hans-Conrad

    2000-12-01

    A new class of M(II)-Hg(II) (M=Cu(II), Co(II), Ni(II)) mixed-metal coordination polymers, Cu(2-pyrazinecarboxylate) 2HgCl 2 ( 4), [Co(2-pyrazinecarboxylate) 2(HgCl 2) 2] · 0.61H 2O ( 5) and [Ni(2-pyrazinecarboxylate) 2(HgCl 2) 2] · 0.77H 2O ( 6), have been prepared by self assembly of metal-containing building blocks, M(2-pyrazinecarboxylate) 2 · (H 2O) 2 (M=Cu(II), Co(II), Ni(II)), with HgCl 2. Compounds 4- 6 were characterized fully by IR, elemental analysis and single crystal X-ray diffraction. Compound 4 crystallized in the monoclinic space group C2/ c, with a=17.916(5) Å, b=7.223(2) Å, c=13.335(4) Å, β=128.726(3)°, V=1346.2(6) Å 3, Z=4. It contains alternating Hg(II) and Cu(II) metal centers that are cross-linked by 2-pyrazinecarboxylate spacers and chlorine co-ligands to generate a unique three-dimensional Hg(II)-Cu(II) mixed metal framework. Compound 5 crystallized in the triclinic space group P1¯, with a=6.3879(7) Å, b=6.6626(8) Å, c=13.2286(15) Å, α=96.339(2)°, β=91.590(2)°, γ=113.462(2)°, V=511.71(10) Å 3, Z=1. Compound 6 also crystallized in the triclinic space group P1¯, with a=6.3543(8) Å, b=6.6194(8) Å, c=13.2801(16) Å, α=96.449(2)°, β=92.263(2)°, γ=113.541(2)°, V=506.67(11) Å 3, Z=1. Compounds 5 and 6 are isostructural and in the solid state the Hg(II)⋯M(II)⋯Hg(II) units are connected by Hg 2Cl 2 linkages to produce a novel M(II)-Hg(II) (MCo(II), Ni(II)) zigzag mixed-metal chain, in which a new type of M-M'-M'-M array was observed. The metal containing building blocks, M(2-pyrazinecarboxylate) 2 · (H 2O) 2 (MCu(II), Co(II), Ni(II)), exhibit different connectivities to HgCl 2 depending on the metal cation contained within them.

  17. Experimental study on Hg{sup 0} removal from flue gas over columnar MnO{sub x}-CeO{sub 2}/activated coke

    Energy Technology Data Exchange (ETDEWEB)

    Xie, Yine [College of Environmental Science and Engineering, Hunan University, Changsha 410082 (China); Key Laboratory of Environmental Biology and Pollution Control, Hunan University, Ministry of Education, Changsha 410082 (China); Li, Caiting, E-mail: ctli@hnu.edu.cn [College of Environmental Science and Engineering, Hunan University, Changsha 410082 (China); Key Laboratory of Environmental Biology and Pollution Control, Hunan University, Ministry of Education, Changsha 410082 (China); Zhao, Lingkui; Zhang, Jie; Zeng, Guangming; Zhang, Xunan; Zhang, Wei; Tao, Shasha [College of Environmental Science and Engineering, Hunan University, Changsha 410082 (China); Key Laboratory of Environmental Biology and Pollution Control, Hunan University, Ministry of Education, Changsha 410082 (China)

    2015-04-01

    Highlights: • The Hg{sup 0} removal efficiency over columnar MnCe6/activated coke up to 94%. • MnO{sub x} and CeO{sub 2} exhibited a significant synergistic role in Hg{sup 0} removal over MnCe/AC. • Lattice oxygen, chemisorbed oxygen and OH groups on the surface of MnCe/AC contributed to Hg{sup 0} oxidation. • Hg{sup 0} removal mechanisms over MnCe/AC were identified firstly. - Abstract: Mn-Ce mixed oxides supported on commercial columnar activated coke (MnCe/AC) were employed to remove elemental mercury (Hg{sup 0}) at low temperatures (100–250 °C) without the assistance of HCl in flue gas. The samples were characterized by X-ray diffraction (XRD), Brunauer–Emmett–Teller (BET), X-ray photoelectron spectroscopy (XPS) and temperature programmed desorption (TPD). Effects of some factors, including Mn-Ce loading values, active component, reaction temperatures and flue gas components (O{sub 2}, SO{sub 2}, NO, H{sub 2}O), on Hg{sup 0} removal efficiency were investigated. Results indicated that the optimal Mn-Ce loading value and reaction temperature were 6% and 190 °C, respectively. Considerable high Hg{sup 0} removal efficiency (>90%) can be obtained over MnCe6/AC under both N{sub 2}/O{sub 2} atmosphere and simulated flue gas atmosphere at 190 °C. Besides, it was observed that O{sub 2} and NO exerted a promotional effect on Hg{sup 0} removal, H{sub 2}O exhibited a suppressive effect, and SO{sub 2} hindered Hg{sup 0} removal seriously when in the absence of O{sub 2}. Furthermore, the XPS spectra of Hg 4f and Hg-TPD results showed that the captured mercury were existed as Hg{sup 0} and HgO on the MnCe6/AC, and HgO was the major species, which illustrated that adsorption and catalytic oxidation process were included for Hg{sup 0} removal over MnCe6/AC, and catalytic oxidation played the critical role. What's more, both lattice oxygen and chemisorbed oxygen or OH groups on MnCe6/AC contributed to Hg{sup 0} oxidation. MnCe6/AC, which exhibited

  18. Superdeformation studies in {sup 191}Hg

    Energy Technology Data Exchange (ETDEWEB)

    Carpenter, M.P.; Janssens, R.V.F.; Crowell, B. [and others

    1995-08-01

    Superdeformation in the A {approximately} 190 region was first observed in {sup 191}Hg from an experiment performed at ATLAS using the Argonne Notre Dame {gamma}-ray facility. We recently revisited the study of superdeformation in this nucleus using Gammasphere and the {sup 160}Gd({sup 36}S,5n) and {sup 174}Yb({sup 22}Ne,5n) reactions at 172 and 120 MeV in order to populate and measure states in the second well. The goal of the experiment was to identify new bands in the data, and thus allow us to gain understanding on the relative placement of single particle orbitals near the N = 112 SD shell gap. From an analysis of the data, the three previously identified SD bands were extended, and their feeding into the yrast states delineated. Two new SD bands were observed and preliminary evidence for a third new band was obtained as well.

  19. HgCdTe monolithic infrared detector

    Energy Technology Data Exchange (ETDEWEB)

    Yakushev, Maxim V.; Dvoretsky, Sergei A.; Kozlov, Alexander I.; Sabinina, Irina V.; Sidorov, Yu.G.; Sorochkin, Alexander V.; Fomin, Boris I.; Aseev, Alexander L. [A.V. Rzhanov Institute of Semiconductor Physics, Siberian Branch RAS, Novosibirsk (Russian Federation)

    2010-06-15

    We report the processes of fabricating monolithic 32 x 32 infrared detector based on (310) HgCdTe/CdTe/ZnTe/ Si photosensitive heterostructure which was grown by a molecular-beam epitaxy technique in the free surface of ROIC cells. Optimum parameters of the technological processes were determined. The minimum temperature of preepitaxial thermal annealing in vacuum of ROIC was determined as 450 C. The dark and photo current-voltage characteristics were measured and analyzed. A good sensitivity of diodes was observed. The product R{sub 0} x A {proportional_to} 10{sup 5} Ohm x cm{sup 2}. (copyright 2010 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  20. Mass loading of Hg in the Monte Amiata mining district, Southern Tuscany (Italy)

    OpenAIRE

    Rimondi V.; Costagliola P.; Gray J. E.; Lattanzi P.; Nannucci M.; Salvadori A.; Vaselli O.

    2013-01-01

    Mercury (Hg) transport in natural environments is of concern because Hg bioaccumulates in the food web. Particularly methyl-Hg is the form of Hg of major concern as it is highly toxic to humans and is ingested through food consumption, dominantly fish. Quantification of Hg mass loads in watersheds draining Hg mine districts allows (1) the identification of sources of contamination, (2) the evaluation of the effect of Hg on the environment, and (3) the identification of processes affecting Hg ...

  1. Synthesis, Characterization and Thermal Studies of Zn(II), Cd(II) and Hg(II) Complexes of N-Methyl-N-Phenyldithiocarbamate: The Single Crystal Structure of [(C6H5)(CH3)NCS2]4Hg2

    Science.gov (United States)

    Onwudiwe, Damian C.; Ajibade, Peter A.

    2011-01-01

    Zn(II), Cd(II) and Hg(II) complexes of N-methyl-N-phenyl dithiocarbamate have been synthesized and characterized by elemental analysis and spectral studies (IR, 1H and 13C-NMR). The single crystal X-ray structure of the mercury complex revealed that the complex contains a Hg centre with a distorted tetrahedral coordination sphere in which the dinuclear Hg complex resides on a crystallographic inversion centre and each Hg atom is coordinated to four S atoms from the dithiocarbamate moiety. One dithiocarbamate ligand acts as chelating ligand while the other acts as chelating bridging ligand between two Hg atoms, resulting in a dinuclear eight-member ring. The course of the thermal degradation of the complexes has been investigated using thermogravimetric and differential thermal analyses techniques. Thermogravimetric analysis of the complexes show a single weight loss to give MS (M = Zn, Cd, Hg) indicating that they might be useful as single source precursors for the synthesis of MS nanoparticles and thin films. PMID:21673933

  2. Superconductivity above 100 K in compounds containing Hg

    International Nuclear Information System (INIS)

    The results of studies of new Hg based cuprate superconductors are reported. Several members of a new family of (Hg,Tl)(Ba,Sr)Can-2CunOx high temperature superconductors have been synthesized. These compounds, which are analogs to the Hg-Ba-Ca- and Tl-Ba-Ca- layered cuprates, are multi-phased and have superconducting transition temperatures above 100 K. Incorporation of Hg appears to stabilize several of the Tl-compounds, including a double layer Tl/Sr system, in a manner similar to the role that Pb plays in the Tl/Sr- and Bi/Sr-systems. It has been suggested that recent reports of resistive Tc's above 200 K in Hg based samples are due to the presence of free Hg. Magnetization measurements of such a sample confirm this hypothesis

  3. Oxidative stress in MeHg-induced neurotoxicity

    Energy Technology Data Exchange (ETDEWEB)

    Farina, Marcelo, E-mail: farina@ccb.ufsc.br [Departamento de Bioquimica, Centro de Ciencias Biologicas, Universidade Federal de Santa Catarina, Florianopolis, SC (Brazil); Aschner, Michael [Department of Pediatrics, Vanderbilt University Medical Center, Nashville, TN (United States); Department of Pharmacology, Vanderbilt University Medical Center, Nashville, TN (United States); Rocha, Joao B.T., E-mail: jbtrocha@yahoo.com.br [Departamento de Quimica, Centro de Ciencias Naturais e Exatas, Universidade Federal de Santa Maria, Santa Maria, RS (Brazil)

    2011-11-15

    Methylmercury (MeHg) is an environmental toxicant that leads to long-lasting neurological and developmental deficits in animals and humans. Although the molecular mechanisms mediating MeHg-induced neurotoxicity are not completely understood, several lines of evidence indicate that oxidative stress represents a critical event related to the neurotoxic effects elicited by this toxicant. The objective of this review is to summarize and discuss data from experimental and epidemiological studies that have been important in clarifying the molecular events which mediate MeHg-induced oxidative damage and, consequently, toxicity. Although unanswered questions remain, the electrophilic properties of MeHg and its ability to oxidize thiols have been reported to play decisive roles to the oxidative consequences observed after MeHg exposure. However, a close examination of the relationship between low levels of MeHg necessary to induce oxidative stress and the high amounts of sulfhydryl-containing antioxidants in mammalian cells (e.g., glutathione) have led to the hypothesis that nucleophilic groups with extremely high affinities for MeHg (e.g., selenols) might represent primary targets in MeHg-induced oxidative stress. Indeed, the inhibition of antioxidant selenoproteins during MeHg poisoning in experimental animals has corroborated this hypothesis. The levels of different reactive species (superoxide anion, hydrogen peroxide and nitric oxide) have been reported to be increased in MeHg-exposed systems, and the mechanisms concerning these increments seem to involve a complex sequence of cascading molecular events, such as mitochondrial dysfunction, excitotoxicity, intracellular calcium dyshomeostasis and decreased antioxidant capacity. This review also discusses potential therapeutic strategies to counteract MeHg-induced toxicity and oxidative stress, emphasizing the use of organic selenocompounds, which generally present higher affinity for MeHg when compared to the classically

  4. The effect of sulphur in silicate melt on partitioning of Ni and other trace elements

    Science.gov (United States)

    Wood, Bernard; Kiseeva, Ekaterina; Wohlers, Anke

    2016-04-01

    It has been suggested that variations in the sulphur contents of silicate melts affect the partitioning of trace chalcophile elements, particularly Ni, between silicate melt and crystalline phases such as olivine [1]. The general idea is that Ni (and other elements) complex with sulphur dissolved in the melt, thereby stabilising Ni in the melt and reducing the olivine-melt partition coefficient DNi. More recent experiments lead to the assertion that any sulphur effect, if present is small and can be ignored [2]. Experiments aimed at addressing this problem have, however, struggled with the difficulty that the maximum S contents of olivine- precipitating melts do not exceed ~0.5% even at sulphide saturation. Any effect is therefore difficult to establish unequivocally. Here we have taken advantage of the fact that experiments under strongly reducing conditions, where FeO activity in the silicate melt is very low lead to much higher concentrations of S than those associated with olivine precipitation. We have therefore investigated partitioning between sulphide melts and haplobasaltic silicate melt at concentrations of FeO between 0.3 and 10 weight% in order to investigate the "sulphur-effect" on partitioning. At the lowest FeO contents we are able to drive the S content of the melt to 10 weight% enabling the effects to be unequivocally established. We find that partitioning of strongly lithophile elements Nb, Ta, U, REE partition more strongly out of silicate melt as its S content increases. The effect is, surprisingly, predominantly due to the effect of S on the activity coefficient of FeO in the melt. In contrast strongly chalcophile Ni, Cu, Ag partition more strongly into the melt as its S content increases. This is due to a dramatic lowering of the activity coefficients of these elements in the silicate as S increases. Elements which show little effect of S include Pb, Co and In. The results enable us to predict the effects of sulphur on olivine-melt and

  5. HgCdTe e-avalanche photodiode detector arrays

    OpenAIRE

    Anand Singh; Shukla, A. K.; Ravinder Pal

    2015-01-01

    Initial results on the MWIR e-APD detector arrays with 30 μm pitch fabricated on LPE grown compositionally graded p-HgCdTe epilayers are presented. High dynamic resistance times active area (R0A) product 2 × 106 Ω-cm2, low dark current density 4 nA/cm2 and high gain 5500 at -8 V were achieved in the n+-υ-p+ HgCdTe e-APD at 80 K. LPE based HgCdTe e-APD development makes this technology amenable for adoption in the foundries established for the conventional HgCdTe photovoltaic detector arrays w...

  6. HD 30963: a new HgMn star

    CERN Document Server

    Monier, R; Royer, F

    2016-01-01

    Using high dispersion high quality spectra of HD 30963 obtained with the echelle spectrograph SOPHIE at Observatoire de Haute Provence in November 2015, we show that this star, hitherto classified as a B9 III superficially normal star, is actually a new Chemically Peculiar star of the HgMn type. Spectrum synthesis reveals large overabundances of Mn, Sr, Y, Zr , Pt and Hg and pronounced underabundances of He and Ni which are characteristic of HgMn stars. We therefore propose that this interesting object be reclassified as a B9 HgMn star.

  7. Elucidation of the defence mechanism in microalgae Chlorella sorokiniana under mercury exposure. Identification of Hg-phytochelatins.

    Science.gov (United States)

    Gómez-Jacinto, Verónica; García-Barrera, Tamara; Gómez-Ariza, José Luis; Garbayo-Nores, Inés; Vílchez-Lobato, Carlos

    2015-08-01

    Algae and aquatic macrophytes are capable of accumulating heavy metals up to concentrations several orders of magnitude higher than those existing in their surrounding environment. Investigation of mercury toxicology in microalgae is of great interest from ecological point of view, since they could be used as bioindicator to evaluate aquatic ecosystems affected by Hg pollution. In this study, we have performed an exposure experiment focused on the biological response of microalgae Chlorella sorokiniana, a unicellular model organism, to Hg-induced toxicity. The culture was exposed to different concentrations of this element for nine days, namely 0.5, 1, 5 and 10mg L(-1) of HgCl2 (as Hg). To achieve a better understanding of the biological mechanisms triggered by Hg-induced toxicity in this alga a metallomic approach based on SEC-ICP-ORS-MS was applied to survey biomarkers of biological response to mercury contamination in surface water. In addition, the combination of RP-HPLC-ICP-ORS-MS and RP-HPLC-ESI-QqQ-TOF-MS was applied to identify, for the first time, two Hg-binding phytochelatins in this aquatic organism, using cell extracts from microalgae exposed to inorganic mercury.

  8. Hg-coordination studies of oligopeptides containing cysteine, histidine and tyrosine by $^{199m}$Hg-TDPAC

    CERN Document Server

    Ctortecka, B; Mallion, S; Butz, T; Hoffmann, R

    1999-01-01

    In order to study the interaction of histidine- and tyrosine- containing peptide chains with Hg(II), the nuclear quadrupole interaction (NQI) of /sup 199m/Hg in the Hg complexes of the oligopeptides alanyl-alanyl-histidyl-alanyl-alanine-amid (AAHAA-NH /sub 2/) and alanyl-alanyl-tyrosyl-alanyl-alanine-amid (AAYAA-NH/sub 2/) was determined by time differential perturbed angular correlation and is compared with previous data on alanyl-alanyl-cysteyl-alanyl- alanyl (AACAA-OH). The /sup 199m/Hg-NQIs depend on the oligopeptide to Hg(II) stoichiometry and indicate that two-fold and four-fold coordinations occur for the bound Hg(II). (12 refs).

  9. Mass loading of Hg in the Monte Amiata mining district, Southern Tuscany (Italy

    Directory of Open Access Journals (Sweden)

    Rimondi V.

    2013-04-01

    Full Text Available Mercury (Hg transport in natural environments is of concern because Hg bioaccumulates in the food web. Particularly methyl-Hg is the form of Hg of major concern as it is highly toxic to humans and is ingested through food consumption, dominantly fish. Quantification of Hg mass loads in watersheds draining Hg mine districts allows (1 the identification of sources of contamination, (2 the evaluation of the effect of Hg on the environment, and (3 the identification of processes affecting Hg transport. This study focuses on the determination of Hg loads in the Paglia River, which drains the Hg district of Monte Amiata (Italy, world’s 4th largest Hg producing district. Mass loads were determined for total Hg, particulate Hg, and dissolved Hg. Data obtained from two sampling campaigns carried out in 2011 indicated that up to 34 g/d of Hg were transported during the rainy season, of which up to 99% was as particulate Hg. Maximum Hg loads were related to runoff from the Abbadia San Salvatore mine (ASSM, and thus, this mine is the main source of Hg to the Paglia River basin. Data indicate that particulate Hg has been deposited along with river sediment, forming a natural sink where resultant chemical reactions promote conversion of Hg from particulate matter to dissolved Hg. These results suggest that mining of Hg has affected this area. Even today, 30 years after the cessation of mining, considerable amounts of Hg are continuously transported downstream from mined areas by local rivers.

  10. Dynamical evolution of titanium, strontium, and yttrium spots on the surface of the HgMn star HD 11753

    OpenAIRE

    Briquet, Maryline; Korhonen, H.; González, J.F.; Hubrig, S.; Hackman, T.

    2010-01-01

    Aims: We gathered about 100 high-resolution spectra of three typical HgMn (mercury-manganese) stars, HD 11753, HD 53244, and HD 221507, to search for slowly pulsating B-like pulsations and surface inhomogeneous distribution of various chemical elements. Methods: Classical frequency analysis methods were used to detect line profile variability and to determine the variation period. Doppler imaging reconstruction was performed to obtain abundance maps of chemical elements on the stellar surfa...

  11. Analysis of Moderately Siderophile Elements in Angrites: Implications for Core Formation of the Angrite Parent Body

    Science.gov (United States)

    Righter, K.; Shirai, N.; Irving, A.J.

    2009-01-01

    Angrites are an enigmatic group of achondrites, that constitute the largest group of basalts not affiliated with the Moon, Mars or Vesta (HEDs). Chemically, angrites are exceptionally refractory element- enriched (e.g., Al, Ca) and volatile element-depleted (e.g., Na and K) achondrites. Highly volatile siderophile and chalcophile elements (Zn, Ge and Se) may be less depleted than alkalis and Ga taken to imply a fractionation of plagiophile elements. Core formation on the angrite parent body (APB) is not well understood due to the dearth of moderately siderophile element (Ga, Ge, Mo, Sb, W) data for angrites, with the exception of Ni and Co [2]. In particular, there are no data for Mo abundances of angrites, while Sb and W abundances are reported for only 3 angrites, and have not always been determined on the same sample. The recent increase in angrite numbers (13) has greatly increased our knowledge of the compositional diversity of the angrite parent body (APB). In this study, we report new Co, Ni, Ga, Mo, Sb and W abundances for angrites by laser ablation inductively coupled plasma mass spectrometry (ICP-MS) in order to place constraints on core formation of the APB.

  12. The Liquid-Liquid Extraction of Toxic Metals (Cd, Hg and Pb by Calixarenes

    Directory of Open Access Journals (Sweden)

    D. Max Roundhill

    2009-12-01

    Full Text Available Toxic metals (Cd, Hg and Pb are mostly present in the environment due to natural phenomenon and human activities as well. Exposure of these non-essential elements in the environment causes severe effects. They are known to cause problems in humans as well as in aquatic life. In this work, we demonstrate various studies regarding liquid-liquid extraction of selected ions with different functionalized calixarenes. This review article briefly discusses several molecular designs of calixarenes for divalent ion (Cd2+, Hg2+ and Pb2+ recognition; as well as the relationship between structure and selectivity of the macrocycles is elaborated. The article does not, however, attempt to cover all of the different approaches to these toxic metal ions extraction.

  13. Assessment of Cu, Pb and Hg Contamination in Bottom Sediments Of Surface Water in XuZhou

    Institute of Scientific and Technical Information of China (English)

    王晓; 韩宝平; 朱雪强

    2004-01-01

    Pollution of heavy metals Cu,Pb and Hg is assessed using geo-accumulation index in this paper. The result shows that the bottom sediments of surface water in Xuzhou is polluted by these heavy metals to deferent degrees, of which the Jinma River is the most serious, and then the Kuihe River, the abandoned Yellow River, and the Jinghang Canal. The Yunlong Lake has also been polluted by Hg. The three kinds of heavy metals in the order of concentration is Hg>Cu>Pb. The pollution degree and the type of element is closely related with industrial structure in Xuzhou.

  14. Factors influencing the large-scale distribution of Hg° in the Mexico City area and over the North Pacific

    OpenAIRE

    Talbot, R.; H. Mao; E. Scheuer; J. Dibb; Avery, M.; Browell, E.; Sachse, G.; S. Vay; D. Blake; Huey, G.; H. Fuelberg

    2008-01-01

    Gas-phase elemental mercury (Hg°) was measured aboard the NASA DC-8 aircraft during the Intercontinental Chemical Transport Experiment Phase B (INTEX-B) campaign in spring 2006. Flights were conducted around Mexico City and on two subsequent deployments over the North Pacific based out of Honolulu, Hawaii and Anchorage, Alaska. Data obtained from 0.15–12 km altitude showed that Hg° exhibited a relatively constant vertical profile centered around 100 ppqv. Highl...

  15. Factors influencing the large-scale distribution of Hg° in the Mexico City area and over the North Pacific

    OpenAIRE

    D. Blake; S. Vay; Sachse, G.; Browell, E.; Avery, M.; J. Dibb; E. Scheuer; H. Mao; Talbot, R.; Huey, G.; H. Fuelberg

    2007-01-01

    Gas-phase elemental mercury (Hg°) was measured aboard the NASA DC-8 aircraft during the Intercontinental Chemical Transport Experiment Phase B (INTEX-B) campaign in spring 2006. Flights were conducted around Mexico City and on two subsequent deployments over the North Pacific based out of Honolulu, Hawaii and Anchorage, Alaska. Data obtained from 0.15–12 km altitude showed that Hg° exhibited a relatively constant vertical profile centered around 100 ppqv. Highly concentrated pol...

  16. Factors influencing the large-scale distribution of Hg° in the Mexico City area and over the North Pacific

    OpenAIRE

    Talbot, R.; H. Mao; E. Scheuer; J. Dibb; Avery, M.; Browell, E.; Sachse, G.; S. Vay; D. Blake; Huey, G.; H. Fuelberg

    2008-01-01

    International audience Gas-phase elemental mercury (Hg°) was measured aboard the NASA DC-8 aircraft during the Intercontinental Chemical Transport Experiment Phase B (INTEX-B) campaign in spring 2006. Flights were conducted around Mexico City and on two subsequent deployments over the North Pacific based out of Honolulu, Hawaii and Anchorage, Alaska. Data obtained from 0.15?12 km altitude showed that Hg° exhibited a relatively constant vertical profile centered around 100 ppqv. Highly conc...

  17. Theoretical chemistry for chemical identification of the heaviest elements

    Science.gov (United States)

    Pershina, V.; Bastug, T.; Anton, J.; Fricke, B.

    2007-05-01

    Adsorption of element 112 on various types of surfaces was studied on the basis of fully relativistic four-component Density-Functional Theory (DFT) electronic structure calculations for atoms, dimers and atom-cluster systems. Using models of localized and mobile adsorption, the equilibrium adsorption temperature for element 112 is predicted with respect to that of Hg on quartz and gold surfaces. On quartz, element 112 should be stronger adsorbed than Hg by about 5 kJ/mol (or by 5 degrees higher temperatures) due to the stronger van der Walls interaction. This is caused by the relativistically contracted smallest atomic radius of element 112. On surface of gold, element 112 should be weaker adsorbed than Hg by about 20 kJ/mol, i.e., at about 100 degrees lower temperatures than Hg. The predicted similarity to Hg indicates that element 112 should be a transition metal forming intermetallic compounds with Au and other metals due to the relatively large involvement of the relativistically destabilized 6d orbitals in bonding. The difference in adsorption enthalpy between Hg and element 112 depends, however, on the adsorption position.

  18. Reduced leakage currents of CdZnTe radiation detectors with HgTe/HgCdTe superlattice contacts

    Science.gov (United States)

    Chang, Y.; Grein, C. H.; Becker, C. R.; Huang, J.; Ghosh, S.; Aqariden, F.; Sivananthan, S.

    2012-10-01

    Room-temperature-operating CdZnTe radiation detectors have high energy resolution, linear energy response and are capable of operating in normal counting and spectroscopic modes, hence are highly desirable for medical diagnosis, nondestructive industrial evaluations, homeland security, counterterrorism inspections and nuclear proliferation detection to ensure national and international nuclear safety. HgTe/HgCdTe superlattices can be designed to selectively transport one carrier species while hindering transport of the other. Specifically, one designs a large carrier effective mass for undesired carriers in the electric field direction, which results in low carrier velocities, and yet a density of states for undesired carrier that is lower than that of a comparable bulk semiconductor, which results in low carrier concentrations, hence a low current density under an electric field. The opposite carrier species can be designed to have a large velocity and high density of states, hence producing a large current density. By employing HgTe/HgCdTe superlattices as contact layers intermediate between CdZnTe absorbers and metal contacts, leakage currents under high electric fields are reduced and improved x-ray and γ-ray detector performance is anticipated. Pixilated CdZnTe radiation detectors arrays were fabricated and characterized to evaluate the effectiveness of HgTe/HgCdTe superlattices in reducing leakage currents. Current-voltage characteristics show that HgTe/HgCdTe superlattice contact layers consistently result in significantly reduced leakage currents relative to detectors with only metal contacts.

  19. Characterization of CdTe, HgTe, and Hg1-xCdxTe grown by chemical beam epitaxy

    Science.gov (United States)

    Wagner, B. K.; Rajavel, D.; Benz, R. G.; Summers, C. J.

    1991-10-01

    Detailed characterization of chemical beam epitaxially (CBE) grown CdTe and Hg1-xCdxTe layers are reported. These characterizations include photoluminescence, infrared transmission, energy dispersive x-ray analysis, and variable temperature (10-300 K) Hall effect and resistivity measurements. The results indicate that high quality HgCdTe layers can be grown by CBE.

  20. Numerical modeling of HgCdTe solidification: effects of phase diagram double-diffusion convection and microgravity level

    Science.gov (United States)

    Bune, Andris V.; Gillies, Donald C.; Lehoczky, Sandor L.

    1997-07-01

    A numerical model of HgCdTe solidification was implemented using finite the element code FIDAP. Model verification was done using both experimental data and numerical test problems. The model was used to eluate possible effects of double- diffusion convection in molten material, and microgravity level on concentration distribution in the solidified HgCdTe. Particular attention was paid to incorporation of HgCdTe phase diagram. It was found, that below a critical microgravity amplitude, the maximum convective velocity in the melt appears virtually independent on the microgravity vector orientation. Good agreement between predicted interface shape and an interface obtained experimentally by quenching was achieved. The results of numerical modeling are presented in the form of video film.

  1. Hg localisation in Tillandsia usneoides L. (Bromeliaceae), an atmospheric biomonitor

    Energy Technology Data Exchange (ETDEWEB)

    Filho, G.M.A. [Instituto de Pesquisas Jardim Botanico do Rio de Janeiro (Brazil). Programa Zona Costeira; Andrade, L.R.; Farina, M. [Cidade Universitaria, Rio de Janeiro (Brazil). Instituto de Ciencias Biomedicas, Departamento de Anatomia; Malm, O. [Cidade Universitaria, Rio de Janeiro (Brazil). Instituto de Biofisica Carlos Chagas Filho, Laboratorio de Radioisotopos Eduardo Penna Franca

    2002-07-01

    The Spanish moss, Tillandsia usneoides, has been applied as an atmospheric biomonitor of Hg contamination, although the mechanism of metal plant accumulation has not been understood until now. In the present work, analytical scanning electron microscopy (SEM) was used to localize Hg in T. usneoides exposed to a Hg-air-contaminated area during 15 days. After this period, Hg was determined by the flow injection mercury system, and plants were prepared for SEM observation and energy-dispersive X-ray analysis. A concentration of 2702{+-}318{mu}g Hgg{sup -1} was determined in exposed plants. The presented microanalytical results demonstrated that Hg was partly associated with atmospheric particles deposited upon the plant surface, but it was highly absorbed by the scales, stem and leaves surfaces and less absorbed by epidermal cells of T. usneoides. No Hg was detected in mesophyll parenchyma or in vascular system cells. The great surface adsorption area provided by the scales, in addition to the characteristics of T. usneoides morphology, especially of the node region, are suggested to confer the great capability of T. usneoides in Hg holding. (author)

  2. Atmospheric gaseous elemental mercury (GEM) concentrations and mercury depositions at a high-altitude mountain peak in south China

    OpenAIRE

    X. W. Fu; Feng, X.; Dong, Z. Q.; R. S. Yin; Wang, J. X.; Yang, Z. R.; Zhang, H.

    2010-01-01

    China is regarded as the largest contributor of mercury (Hg) to the global atmospheric Hg budget. However, concentration levels and depositions of atmospheric Hg in China are poorly known. Continuous measurements of atmospheric gaseous elemental mercury (GEM) were carried out from May 2008 to May 2009 at the summit of Mt. Leigong in south China. Simultaneously, deposition fluxes of THg and MeHg in precipitation, throughfall and litterfall were also studied. Atmospheric GEM concentrations aver...

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

    Energy Technology Data Exchange (ETDEWEB)

    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.

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

    International Nuclear Information System (INIS)

    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 (207Pb/206Pb = 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 (87Sr/86Sr = 0.70859 to 0.71155) are likely related to coal fly ash and soil dust. Mercury isotope ratios (δ202Hg = − 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

  5. Summary Abstract: HgTe–CdTe superlattices

    OpenAIRE

    McGill, T. C.; Smith, D L

    1983-01-01

    In their seminal paper on superlattices, Esaki and Tsu indicated that superlattices involving II-VI compounds and their alloys, could be of interest along with superlattices involving Group IV and III-V semiconductors. Independently, Schulman and McGill identified the Hg-Te-CdTe superlattice as an interesting case to study. HgTe and CdTe have the same crystal structure and lattice constrant to 0.3%. CdTe is a conventional zinc blende semiconductor with a band gap of about 1.6 eV; HgTe is a ze...

  6. Hg and Se Speciation in Liver Tissue of Marine Birds

    International Nuclear Information System (INIS)

    X-ray fluorescence microprobe maps of Hg and Se distribution were made on liver tissue slices from marine birds (Cormorants) from Florida's Everglades. The birds bio-concentrate these toxic pollutants that are ingested from their diet of fish. The fluorescence maps show strong localization of Mercury and Selenium into 'hot spots' less than 100 microns in size. XAFS measurements were made on hot spots to demonstrate that the Hg and Se are indeed are chemically bound, supporting the idea that moderate levels of Se may have a protective effect against Hg through its complexation.

  7. Comparison of total Hg results in sediment samples from Rio Grande reservoir determine by NAA and CV AAS

    Energy Technology Data Exchange (ETDEWEB)

    Franklin, Robson L., E-mail: robsonf@cetesbnet.sp.gov.br [Centro Tecnologico de Saneamento Basico (ELAI/CETESB), SP, Sao Paulo (Brazil). Laboratorio de Quimica Inorganica; Bevilacqua, Jose Eduardo [Centro Tecnologico de Saneamento Basico (CETESB), SP, Sao Paulo (Brazil). UNIFIEO - Centro Universitario FIEO; Favaro, Deborah I.T., E-mail: defavaro@ipen.br [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil). Laboratorio de Analise por Ativacao Neutronica (LAN/CRPq)

    2011-07-01

    The Rio Grande reservoir is located in the Metropolitan area of Sao Paulo and it is used for recreation purposes and as source water for drinking water production. During the last decades has been detected mercury contamination in the sediments of this reservoir, mainly in the eastern part, near the main affluent of the reservoir, in the Rio Grande da Serra and Ribeirao Pires counties. In the present study bottom sediment samples were collected in four different sites into four sampling campaigns during the period of September 2008 to January 2010. The samples were dried at room temperature, ground and passed through a 2 mm sieve. Total Hg determination in the sediment samples was carried out by two different analytical techniques: neutron activation analysis (NAA) and cold vapor atomic absorption spectrometry (CV AAS). The methodology validation, in terms of precision and accuracy, was performed by reference materials, and presented a recovery of 83 to 108%. The total Hg results obtained by both analytical techniques ranged from 3 to 71 mg kg-1 and were considered similar by statistical analysis, even though NAA technique furnishes the total concentration while CV AAS using the 3015 digestion procedure characterizes only the bioavailable Hg. These results confirm that both analytical techniques were suitable to detect the Hg concentration levels in the Rio Grande sediments studied. The Hg levels in the sediment of the Rio Grande reservoir confirm the anthropogenic origin for this element in this ecosystem. (author)

  8. Trace element emissions from coal

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2012-09-15

    Trace elements are emitted during coal combustion. The quantity, in general, depends on the physical and chemical properties of the element itself, the concentration of the element in the coal, the combustion conditions and the type of particulate control device used, and its collection efficiency as a function of particle size. Some trace elements become concentrated in certain particle streams following combustion such as bottom ash, fly ash, and flue gas particulate matter, while others do not. Various classification schemes have been developed to describe this partitioning behaviour. These classification schemes generally distinguish between: Class 1: elements that are approximately equally concentrated in the fly ash and bottom ash, or show little or no fine particle enrichment, examples include Mn, Be, Co and Cr; Class 2: elements that are enriched in the fly ash relative to bottom ash, or show increasing enrichment with decreasing particle size, examples include As, Cd, Pb and Sb; Class 3: elements which are emitted in the gas phase (primarily Hg (not discussed in this review), and in some cases, Se). Control of class 1 trace elements is directly related to control of total particulate matter emissions, while control of the class 2 elements depends on collection of fine particulates. Due to the variability in particulate control device efficiencies, emission rates of these elements can vary substantially. The volatility of class 3 elements means that particulate controls have only a limited impact on the emissions of these elements.

  9. Magnetotransport in double quantum well with inverted energy spectrum: HgTe/CdHgTe

    Science.gov (United States)

    Yakunin, M. V.; Suslov, A. V.; Popov, M. R.; Novik, E. G.; Dvoretsky, S. A.; Mikhailov, N. N.

    2016-02-01

    We present an experimental study of the double-quantum-well (DQW) system made of two-dimensional layers with inverted energy band spectrum: HgTe. The magnetotransport reveals a considerably larger overlap of the conduction and valence subbands than in known HgTe single quantum wells (QW), which may be regulated here by an applied gate voltage Vg. This large overlap manifests itself in a much higher critical field Bc separating the range above it with a plain behavior of the Hall magnetoresistance ρx y(B ) , where the quantum peculiarities shift linearly with Vg, and the range below with a complicated behavior. In the latter case, specific structures in ρx y(B ) are formed like a double-N -shaped ρx y(B ) , reentrant sign-alternating quantum Hall effect with transitions into a zero-filling-factor state, etc., which are clearly manifested here due to better magnetic quantization at high fields, as compared to the features seen earlier in a single HgTe QW. The coexisting electrons and holes were found in the whole investigated range of positive and negative Vg as revealed (i) from fits to the low-field N -shaped ρx y(B ) , (ii) from the Fourier analysis of oscillations in ρx x(B ) , and (iii) from a specific behavior of ρx y(B ) at high positive Vg. A peculiar feature here is that the found electron density n remains almost constant in the whole range of investigated Vg while the hole density p drops down from the value a factor of 6 larger than n at extreme negative Vg to almost zero at extreme positive Vg passing through the charge-neutrality point. We show that this difference between n and p stems from an order of magnitude larger density of states for holes in the lateral valence subband maxima than for electrons in the conduction subband minimum. We analyze our observations on the basis of a calculated picture of magnetic levels in a DQW and suggest that their specificity is due to (i) a nonmonotonic course of the valence subband magnetic levels and an

  10. Quantum Calorimeters Based on HgCdTe Alloys Project

    Data.gov (United States)

    National Aeronautics and Space Administration — NASA's next generation of x-ray observation missions require x-ray calorimeters with superior energy resolution. Semimetallic HgTe has already proven itself as an...

  11. Interaction of Hg Atom with Bare Si(111) Surface

    Institute of Scientific and Technical Information of China (English)

    LIU Yong-Jun; LIU Ying

    2006-01-01

    To evaluate the interaction between Hg atom and bare Si(111) surface, three types of silicon cluster models of Si4H7, Si7H10 and Si16H20 together with their Hg complexes were studied by using hybrid (U)B3LYP density functional theory method. Optimized geometries and energies for Hg atom on different adsorption sites indicate that: 1) the binding energies at different adsorption sites are small (ranging from ~3 to 8 kJ/mol dependent on the adsorption sites), suggesting a weak interaction between Hg atom and silicon surface; 2) the most favorable adsorption site is the on top (T) site. By analyzing their natural bonding orbitals, the possible reason of this difference is suggested.

  12. Observation of Broadband Ultraviolet Emission From Hg 3 *

    Science.gov (United States)

    Chen, Wenting; Glavin, Thomas; Eden, James; Laboratory for Optical Physics; Engineering Team

    2016-05-01

    A previously-unobserved emission continuum, peaking at ~ 380 nm, has been observed when Hg vapor is photoexcited at 248 nm (KrF laser). Attributed to the mercury trimer, Hg3, this emission continuum has a spectral breadth (FWHM) which increases from ~ 65 nm to ~ 90 nm when the Hg number density rises from ~1016 cm-3 to ~ 2 ×1019 cm-3. Over the same interval in [Hg], the emission decay rate increases only slightly (~ 6 ×103 s-1 to ~ 7 ×103 s-1). Comparisons of the observed spectrum with theory suggest that the observed continuum is the result of transitions between pairs of electronic states having a linear or equilateral triangular configuration.

  13. Horizontal Branch stars as AmFm/HgMn stars

    CERN Document Server

    Michaud, G

    2008-01-01

    Recent observations and models for horizontal branch stars are briefly described and compared to models for AmFm stars. The limitations of those models are emphasized by a comparison to observations and models for HgMn stars.

  14. No magnetic field in the spotted HgMn star mu Leporis

    CERN Document Server

    Kochukhov, O; Piskunov, N; Jeffers, S V; Johns-Krull, C M; Keller, C U; Rodenhuis, M; Snik, F; Stempels, H C; Valenti, J A

    2011-01-01

    Chemically peculiar stars of the mercury-manganese (HgMn) type represent a new class of spotted late-B stars, in which evolving surface chemical inhomogeneities are apparently unrelated to the presence of strong magnetic fields but are produced by some hitherto unknown astrophysical mechanism. The goal of this study is to perform a detailed line profile variability analysis and carry out a sensitive magnetic field search for one of the brightest HgMn stars - mu Lep. We acquired a set of very high-quality intensity and polarization spectra of mu Lep with the HARPSpol polarimeter. These data were analyzed with the multiline technique of least-squares deconvolution in order to extract information on the magnetic field and line profile variability. Our spectra show very weak but definite variability in the lines of Sc, all Fe-peak elements represented in the spectrum of mu Lep, as well as Y, Sr, and Hg. Variability might also be present in the lines of Si and Mg. Anomalous profile shapes of Ti II and Y II lines s...

  15. Geothermal chemical elements in lichens of Yellowstone National Park

    Science.gov (United States)

    Bennett, J.P.; Wetmore, C.M.

    1999-01-01

    Geothermal features (e.g. geysers, fumaroles, vents, and springs) emit gaseous mercury, sulfur and heavy metals and therefore, are natural sources of these elements in the atmosphere. Field studies of heavy metals in lichens in Italy have detected elevated concentrations near geothermal power plants, and have determined that the origin of mercury is from soil degassing, not soil particles. We studied this phenomenon in a geothermal area without power plants to determine the natural levels of mercury and other elements. Two common and abundant species of epiphytic Lichens, Bryoria fremontii and Letharia vulpina, were collected at six localities in Yellowstone National Park, USA in 1998 and analyzed for 22 chemical elements. Thirteen elements differed significantly between species. Some elements were significantly higher in the southern part of the park, while others were higher in the north. Levels of most elements were comparable with those in other national parks and wilderness areas in the region, except Hg, which was unusually high. The most likely sources of this element are the geothermal features, which are known emitters of Hg. Multivariate analyses revealed strong positive associations of Hg with S, and negative associations with soil elements, providing strong evidence that the Hg in the lichens is the result of soil degassing of elemental Hg rather than particulate Hg directly from soils. Average Hg levels in the lichens were 140 p.p.b. in Bryoria and 110 p.p.b. in Letharia, but maxima were 291 and 243 p.p.b., respectively. In spite of this, both species were healthy and abundant throughout the park.

  16. Measurements of shape co-existence in $^{182,184}$Hg using Coulomb excitation

    CERN Multimedia

    Voulot, D; Paul, E S; Siem, S; Czosnyka, T; Napiorkowski, P J; Iwanicki, J S

    2007-01-01

    We propose to exploit the unique capability of ISOLDE to provide post-accelerated $^{182,184}$Hg ions from the REX facility to enable the lowest states of these nuclei to be Coulomb excited. By measuring the $\\gamma$-ray yields using the MINIBALL array we can measure the transition and diagonal E2 matrix elements for these states. This will give quantitative information about the nature of the shape coexistence in these nuclei and allow the sign of the quadrupole deformation be determined for the first time. We require 24 shifts to fulfill the aims of the experiment.

  17. First observation of excited states in 173Hg93

    CERN Document Server

    O'Donnell, D; Scholey, C; Bianco, L; Capponi, L; Carroll, R J; Darby, I G; Donosa, L; Drummond, M; Ertugral, F; Greenlees, P T; Grahn, T; Hauschild, K; Herzan, A; Jakobsson, U; Jones, P; Joss, D T; Julin, R; Juutinen, S; Ketelhut, S; Labiche, M; Leino, M; Lopez-Martens, A; Mullholland, K; Nieminen, P; Peura, P; Rahkila, P; Rinta-Antila, S; Ruotsalainen, P; Sandzelius, M; Saren, J; Saygi, B; Simpson, J; Sorri, J; Thornthwaite, A; Uusitalo, J

    2012-01-01

    The neutron-deficient nucleus 173Hg has been studied following fusion-evaporation reactions. The observation of gamma rays decaying from excited states are reported for the first time and a tentative level scheme is proposed. The proposed level scheme is discussed within the context of the systematics of neighbouring neutron-deficient Hg nuclei. In addition to the gamma-ray spectroscopy, the alpha decay of this nucleus has been measured yielding superior precision to earlier measurements.

  18. Dynamical evolution of titanium, strontium, and yttrium spots on the surface of the HgMn star HD 11753

    CERN Document Server

    Briquet, M; Gonzalez, J F; Hubrig, S; Hackman, T

    2010-01-01

    Aims. We gathered about 100 high-resolution spectra of three typical HgMn (mercury-manganese) stars, HD 11753, HD 53244, and HD 221507, to search for slowly pulsating B-like pulsations and surface inhomogeneous distribution of various chemical elements. Methods. Classical frequency analysis methods were used to detect line profile variability and to determine the variation period. Doppler imaging reconstruction was performed to obtain abundance maps of chemical elements on the stellar surface. Results. For HD 11753, which is the star with the most pronounced variability, distinct spectral line profile changes were detected for Ti, Sr, Y, Zr, and Hg, whereas for HD 53244 and HD 221507 the most variable line profiles belong to the elements Hg and Y, respectively. We derived rotation periods for all three stars from the variations of radial velocities and equivalent widths of spectral lines belonging to inhomogeneously distributed elements: P_rot (HD 11753)=9.54 d, P_rot (HD 53244)=6.16 d, and P_rot (HD 221507)=...

  19. Self-powered sensor for trace Hg2+ detection.

    Science.gov (United States)

    Wen, Dan; Deng, Liu; Guo, Shaojun; Dong, Shaojun

    2011-05-15

    A self-powered electrochemical sensor has been facilely designed for sensitive detection of Hg(2+) based on the inhibition of biocatalysis process of enzymatic biofuel cell (BFC) for the first time. The as-prepared one-compartment BFC, which was consisted of alcohol dehydrogenase supported on single-walled carbon nanohorns-based mediator system as the anode and bilirubin oxidase as the cathodic biocatalyst, generated an open circuit potential (V(oc)) of 636 mV and a maximum power density of 137 μW cm(-2). It was interestingly found that the presence of Hg(2+) would affect the performance of the constructed BFC (e.g., V(oc)). Taking advantage of the inhibitive effect of Hg(2+), a novel self-powered Hg(2+) sensor has been developed, which showed a linear range of 1-500 nM (R(2) = 0.999) with a detection limit of 1 nM at room temperature. In addition, this BFC-type sensor exhibited good selectivity for Hg(2+) against other common environmental metal ions, and the feasibility of the method for Hg(2+) detection in actual water samples (i.e., tap, ground, and lake water) was demonstrated with satisfactory results.

  20. Factors Influencing the Large-Scale Distribution of Hg(0) in the Mexico City Area and Over the North Pacific

    Science.gov (United States)

    Talbot, R.; Mao, H.; Scheuer, E.; Dibb, J.; Avery, M.; Browell, E.; Sachse, G.; Vay, S.; Blake, D.; Huey, G.; Fuelberg, H.

    2007-12-01

    Gas-phase elemental mercury (Hg°) was measured aboard the NASA DC-8 aircraft during the NASA Intercontinental Chemical Transport Experiment Phase B (INTEX-B) campaign in spring 2006. Flights were conducted around Mexico City and on two subsequent deployments over the North Pacific based out of Honolulu, Hawaii and Anchorage, Alaska. Data was obtained during March-May 2006 and covered 0.15-12 km altitude. The vertical distribution in all three study regions showed that Hg° exhibited a relatively constant mixing ratio centered around 100 ppqv. Highly concentrated pollution plumes emanating from Mexico City revealed that mixing ratios of Hg° as large as 500 ppqv were correlated with combustion tracers such as CO, but not SO2 which is presumably released from coal burning, refineries, and volcanoes. Our analysis of Mexico City plumes indicated that widespread multi-source urban/industrial emissions may have a more important influence on Hg° than specific point sources. Over the Pacific, correlations with CO, CO2, CH4, and C2Cl4 were diffuse overall, but recognizable on flights out of Anchorage and Honolulu. In distinct plumes originating from the Asian continent the Hg° - CO relationship was better defined and yielded an average value of ~0.0050 ng Hg° m-3/ppbv, in good agreement with previous findings. A prominent feature of the INTEX-B dataset was frequent total depletion of Hg° in the upper troposphere when stratospherically influenced air was encountered. When O3 mixing ratios exceeded 300 ppbv, Hg° was rarely detected. It appears that in the tropopause and stratosphere Hg° is oxidized on the order of days followed by heterogeneous transformation to particulate mercury. Our data confirm efficient chemical cycling of Hg° in the tropopause region and show that it is strongly anti-correlated with O3. These processes constitute an effective chemical sink for Hg° at the top of the troposphere, which may recycle mercury back to the gas phase as stratospheric

  1. Long-wavelength infrared photoconductor technology based on epitaxially grown Hg1-xCdxTe

    Science.gov (United States)

    Siliquini, John F.; Fynn, Kevin A.; Musca, Charles A.; Nener, Brett D.; Dell, John M.; Faraone, Lorenzo

    1995-09-01

    The performance of Hg1-xCdxTe long wavelength infrared (LWIR) photoconductors is strongly dependent on the semiconductor surface conditions and contact characteristics. In this paper we review these effects in relation to obtaining an optimum device technology suitable for use in two-dimensional infrared focal plane arrays (IRFPAs) based on the fabrication of high performance LWIR photoconductors on epitaxially grown Hg1-xCdxTe. Although the proposed design can be applied to a variety of epitaxially grown Hg1-xCdxTe material, for optimum performance the starting Hg1-xCdxTe semiconductor consists of epitaxially grown heterostructure layers in which a two-dimensional mosaic of lateral design photoconductors are fabricated. The heterostructure layer provides high performance devices at greatly reduced power dissipation levels, while the unique design allows for the high density integration of photoconductors in a two-dimensional array geometry with high fill factor. The proposed photoconductor array with n+ blocking contacts has been experimentally verified in a 3 X 3 array format with all elements in the array exhibiting background limited infrared photodetector (BLIP) performance at 80 K. Performance issues such as response uniformity, pixel yield, fill factor, crosstalk, power dissipation, detector impedance, array architecture, and maximum array size are discussed in relation to the suitability of the proposed photoconductor structure for use in IRFPA modules. It is found that in many cases the proposed photoconductor technology has the potential to deliver significant advantages, such as higher yield, higher fill factor, better uniformity, less crosstalk, and larger potential array size, in comparison to an IRFPA design based on photovoltaic technology.

  2. Hg0 evasion from boreal mires determined with chamber methods and a novel REA design

    Science.gov (United States)

    Osterwalder, Stefan; Fritsche, Johannes; Åkerblom, Staffan; Nilsson, Mats B.; Alewell, Christine; Bishop, Kevin

    2015-04-01

    Anthropogenic mercury has accumulated in superficial organic soils of boreal mires, hotspots of methylmercury production. We hypothesize that emission from the peat surface is an important factor in regulating the pool of mercury in mires and ultimately the loading of methylmercury to surface waters. To test this hypothesis, we used both dynamic flux chambers (DFCs) and a dual-intake, single analyzer Relaxed Eddy Accumulation (REA) system to quantify the land-atmosphere exchange of elemental mercury (Hg0) from a mixed acid mire system situated near Vindeln in the county of Västerbotten, Sweden. Teflon and polycarbonate DFCs were used to (i) investigate the effect of sulfur and nitrogen addition as well as warming and changed moisture regimes on Hg0 flux and (ii) to quantify typical all-day summertime fluxes. The novel REA design was developed for long-term, all-year flux monitoring and uses twin inlets at the same level for simultaneous accumulation of up and downdrafts on a pair of gold traps which are then analyzed sequentially on the same detector while another pair of gold traps takes over the accumulation. The exchange of Hg0 from the peatland surface was measured continuously with DFC during cloudless conditions in July 2014 and averaged 0.62 ± 1.3 ng m-2 h-1. The flux revealed a significant diurnal pattern and a strong linear relationship with air temperature inside (R2= 0.65, p levels in the soil are too long because up to now the emission of Hg from the mire surface to the atmosphere has been ignored.

  3. Simultaneous determination of Hg(II) and alkylated Hg, Pb, and Sn species in human body fluids using SPME-GC/MS-MS

    Energy Technology Data Exchange (ETDEWEB)

    Dunemann, L.; Hajimiragha, H.; Begerow, J. [Department of Analytical Chemistry, Medizinisches Inst. fuer Umwelthygiene, Duesseldorf (Germany)

    1999-03-01

    A GC/MS-MS method for the determination of Hg(II) and alkylated Hg, Pb, and Sn species in human urine is described. Separation and identification of the metal species are performed by capillary gas chromatography coupled with an ion-trap mass spectrometer with electron impact ionization in the tandem-MS mode. For sample preparation a very promising technique was applied that is based on a derivatization with sodium tetraethylborate followed by headspace solid phase microextraction (SPME). Operation of the used ion trap in the tandem-MS mode yields in improved detection limits because of a signal-to-noise ratio that is at least one order of magnitude better than in the MS mode. The detection limits in real matrices like urine are between 7 and 22 ng/L for all species investigated. Urinary levels of inorganic Hg in non-occupationally exposed persons with and without dental amalgam were found to be between 0.1 and 1.4 {mu}g/L. A reference material (``ClinRep, Level I``) was used for quality assurance. Compared to the coupling of GC with ICP-MS (``inorganic`` MS), the advantage of the proposed method using an ``organic`` MS is that (i) the species can be directly identified via their precursor and daughter ions and (ii) analysis can be performed with a commercially available hyphenated technique at moderate costs and needs no lab-made interfacing. Moreover, it offers a real multi-element/multi-species capability with low detection limits and a minimum of sample preparation. (orig.) With 1 fig., 1 tab., 9 refs.

  4. GNAQPMS-Hg v1.0, a global nested atmospheric mercury transport model: model description, evaluation and application to trans-boundary transport of Chinese anthropogenic emissions

    Directory of Open Access Journals (Sweden)

    H. S. Chen

    2014-10-01

    Full Text Available Atmospheric mercury (Hg is a toxic pollutant and can be transported over the whole globe due to its long lifetime in the atmosphere. For the purpose of assessing Hg hemispheric transport and better characterizing regional Hg pollution, a global nested atmospheric Hg transport model (GNAQPMS-Hg has been developed. In GNAQPMS-Hg, the gas and aqueous phase Hg chemistry representing the transformation among three forms of Hg: elemental mercury (Hg(0, divalent mercury (Hg(II, and primary particulate mercury (Hg(P are calculated. A detailed description of the model, including mercury emissions, gas and aqueous phase chemistry, and dry and wet deposition is given in this study. Worldwide observations including extensive data in China have been collected for model evaluation. Comparison results show that the model reasonably simulates the global mercury budget and the spatial–temporal variation of surface mercury concentrations and deposition. Overall, model predictions of annual total gaseous mercury (TGM and wet deposition agree with observations within a factor of two, and within a factor of five for oxidized mercury and dry deposition. The model performs significantly better in North America and Europe than in East Asia. This can probably be attributed to the large uncertainties in emission inventories, coarse model resolution and to the inconsistency between the simulation and observation periods in East Asia. Compared to the global simulation, the nested simulation shows improved skill at capturing the high spatial variability of Hg concentrations and deposition over East Asia. In particular, the root mean square error (RMSE of simulated Hg wet deposition over East Asia is reduced by 24% in the nested simulation. Model sensitivity studies indicate that Chinese primary anthropogenic emissions account for 30 and 62% of surface mercury concentrations and deposition over China, respectively. Along the rim of the western Pacific, the contributions

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

    Science.gov (United States)

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

    2016-05-01

    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 (Hg10In90, Hg30In70,. Hg50In50, Hg70In30, and Hg90Pb10) 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.

  6. Earthworm casts as a sampling medium – a case study from highly contaminated Hg roasting site Pšenk (Idrija area, Slovenia

    Directory of Open Access Journals (Sweden)

    Tamara Teršič

    2013-12-01

    Full Text Available In this study an interesting sampling medium - earthworm casts was examined in a highly Hg contaminated area. Enrichment factor (EF has been applied to assess elevated concentrations of analyzed elements in earthworm casts and to determine elevated concentrations of these elements in soils and casts with regard to European average concentrations in topsoil. In a previous study (Teršič & Gosar, 2012 it was shown that Hg contents and dispersion in casts from studied roasting site are comparable to those in soil, which indicates that soil contamination is substantially reflected in contamination of earthworm casts. Therefore the comparison between elemental concentrations in earthworm casts and soil was investigated with the intention to assess the reflection of possible soil contamination in casts. Besides Hg contamination, elevated concentrations of As, Ca, Cd, Mo, Pb and U were also determined in earthworm casts. The calculated EFs show moderate enrichment of casts with Ca, Sr and P and minimal enrichment with Mg, Zn and Cu. Cast, SOM (surface organic matter rich soil layer and soil enrichments with regard to the European averages show extreme enrichment of all studied media with Hg, followed by significant enrichment with Mo and Cd and moderate enrichment with As. Spatial distributions of analyzed elements in casts mostly show similar pattern as in soil, however, because of the different nature of different earthworm species and specific properties of different elements, the data about cast contamination can only serve as an approximate prediction about the dispersion and distribution of contaminant in soil.

  7. Probabilistic meta-analysis of risk from the exposure to Hg in artisanal gold mining communities in Colombia

    OpenAIRE

    Miguel García, Eduardo de; Ortega Romero, Marcelo; Gómez San Martín, Amaia; Clavijo, Diana

    2014-01-01

    Colombia is one of the largest per capita mercury polluters in the world as a consequence of its artisanal gold mining activities. The severity of this problem in terms of potential health effects was evaluated by means of a probabilistic risk assessment carried out in the twelve departments (or provinces) in Colombia with the largest gold production. The two exposure pathways included in the risk assessment were inhalation of elemental Hg vapors and ingestion of fish contaminated with methyl...

  8. 187Re-187Os systematics, highly siderophile element, S-Se-Te abundances in the components of unequilibrated L chondrites

    Science.gov (United States)

    Kadlag, Yogita; Becker, Harry

    2016-01-01

    The 187Re-187Os systematics, abundances of highly siderophile elements (HSE: Re, platinum group elements and Au), Te, Se and S as well as major and minor elements were determined in separated components of two unequilibrated L chondrites QUE 97008 (L3.05) and Ceniceros (L3.7). The 187Re-187Os systematics are disturbed in the components of both meteorites, most likely due to open system behavior of Re during terrestrial weathering of QUE 97008 and alteration on the L chondrite parent body as indicated by an internal errorchron generated for components of Ceniceros. The HSE abundance patterns suggest that the bulk rock abundances were mainly controlled by two different end members. Non-magnetic fractions display lower Re/Os and HSE/Ir than CI chondrites. Chondrules, metal-troilite spherules and fine magnetic fractions, are depleted in refractory HSE and show higher Rh/Ir, Pd/Ir and Au/Ir than in CI chondrites. The different HSE compositions indicate the presence of unequilibrated alloys and loss of refractory HSE-rich carrier phases from the precursors of some L chondrite components. Gold is decoupled from other HSE in magnetic fractions and shows chalcophile affinities with a grain size dependent variation similar to S and Se, presumably inherited from preaccretionary processes. Tellurium is depleted in all components compared to other analysed siderophile elements, and its abundance was most likely controlled by fractional condensation and different geochemical affinities. The volatility dependent depletion of Te requires different physical and chemical conditions than typical for the canonical condensation sequence as represented by carbonaceous chondrites. Tellurium also shows variable geochemical behavior, siderophile in Ceniceros, predominantly chalcophile in QUE 97008. These differences may have been inherited from element partitioning during chondrule formation. Selenium and S on the other hand are almost unfractionated from each other and only show

  9. Mercury (Hg) burden in children: The impact of dental amalgam

    International Nuclear Information System (INIS)

    The risks and benefits of using mercury (Hg) in dental amalgam have long been debated. This study was designed to estimate Hg body burden and its association with dental amalgam fillings in 182 children (ages: 5-15 years) living in Taif City. Hg was measured in urine (UHg), hair (HHg) and toenails (NHg) by the Atomic Absorption Spectrophotometer with Vapor Generator Accessory system. Urinary Hg levels were calculated as both micrograms per gram creatinine (μg/g creatinine) and micrograms per liter (μg/L). We found that children with amalgam fillings (N = 106) had significantly higher UHg-C levels than children without (N = 76), with means of 3.763 μg/g creatinine versus 3.457 μg/g creatinine, respectively (P = 0.019). The results were similar for UHg (P = 0.01). A similar pattern was also seen for HHg, with means of 0.614 μg/g (N = 97) for children with amalgam versus 0.242 μg/g (N = 74) for those without amalgam fillings (P = 0). Although the mean NHg was higher in children without amalgam (0.222 μg/g, N = 61) versus those with (0.163 μg/g, N = 101), the relationship was not significant (P = 0.069). After adjusting for many confounders, the multiple logistic regression model revealed that the levels of UHg-C and HHg were 2.047 and 5.396 times higher, respectively, in children with dental amalgam compared to those without (P < 0.01). In contrast, a significant inverse relationship was seen between NHg levels and dental amalgam fillings (P = 0.003). Despite the controversy surrounding the health impact of dental amalgam, this study showed some evidence that amalgam-associated Hg exposure might be related with symptoms of oral health, such as aphthous ulcer, white patches, and a burning-mouth sensation. Further studies are needed to reproduce these findings. The present study showed that significant numbers of children with or without amalgam had Hg levels exceeding the acceptable reference limits. The detrimental neurobehavioral and/or nephrotoxic effects of

  10. Mercury (Hg) burden in children: The impact of dental amalgam

    Energy Technology Data Exchange (ETDEWEB)

    Al-Saleh, Iman, E-mail: iman@kfshrc.edu.sa [Biological and Medical Research Department, King Faisal Specialist Hospital and Research Centre, PO Box: 3354, Riyadh 11211 (Saudi Arabia); Al-Sedairi, Al anoud [Department of Zoology, College of Science, King Saud University, PO Box: 24452, Riyadh 11495 (Saudi Arabia)

    2011-07-15

    The risks and benefits of using mercury (Hg) in dental amalgam have long been debated. This study was designed to estimate Hg body burden and its association with dental amalgam fillings in 182 children (ages: 5-15 years) living in Taif City. Hg was measured in urine (UHg), hair (HHg) and toenails (NHg) by the Atomic Absorption Spectrophotometer with Vapor Generator Accessory system. Urinary Hg levels were calculated as both micrograms per gram creatinine ({mu}g/g creatinine) and micrograms per liter ({mu}g/L). We found that children with amalgam fillings (N = 106) had significantly higher UHg-C levels than children without (N = 76), with means of 3.763 {mu}g/g creatinine versus 3.457 {mu}g/g creatinine, respectively (P = 0.019). The results were similar for UHg (P = 0.01). A similar pattern was also seen for HHg, with means of 0.614 {mu}g/g (N = 97) for children with amalgam versus 0.242 {mu}g/g (N = 74) for those without amalgam fillings (P = 0). Although the mean NHg was higher in children without amalgam (0.222 {mu}g/g, N = 61) versus those with (0.163 {mu}g/g, N = 101), the relationship was not significant (P = 0.069). After adjusting for many confounders, the multiple logistic regression model revealed that the levels of UHg-C and HHg were 2.047 and 5.396 times higher, respectively, in children with dental amalgam compared to those without (P < 0.01). In contrast, a significant inverse relationship was seen between NHg levels and dental amalgam fillings (P = 0.003). Despite the controversy surrounding the health impact of dental amalgam, this study showed some evidence that amalgam-associated Hg exposure might be related with symptoms of oral health, such as aphthous ulcer, white patches, and a burning-mouth sensation. Further studies are needed to reproduce these findings. The present study showed that significant numbers of children with or without amalgam had Hg levels exceeding the acceptable reference limits. The detrimental neurobehavioral and

  11. Overcoming phytoremediation limitations. A case study of Hg contaminated soil

    Science.gov (United States)

    Barbafieri, Meri

    2013-04-01

    Phytoremediation is a broad term that comprises several technologies to clean up water and soil. Despite the numerous articles appearing in scientific journals, very few field applications of phytoextraction have been successfully realized. The research here reported on Phytoextraction, the use the plant to "extract" metals from contaminated soil, is focused on implementations to overcome two main drawbacks: the survival of plants in unfavorable environmental conditions (contaminant toxicity, low fertility, etc.) and the often lengthy time it takes to reduce contaminants to the requested level. Moreover, to overcome the imbalance between the technology's potential and its drawbacks, there is growing interest in the use of plants to reduce only the fraction that is the most hazardous to the environment and human health, that is to target the bioavailable fractions of metals in soil. Bioavailable Contaminant Stripping (BCS) would be a remediation approach focused to remove the bioavailable metal fractions. BCS have been used in a mercury contaminated soil from Italian industrial site. Bioavailable fractions were determined by sequential extraction with H2O and NH4Cl.Combined treatments of plant hormone and thioligand to strength Hg uptake by crop plants (Brassica juncea and Helianthus annuus) were tested. Plant biomass, evapotranspiration, Hg uptake and distribution following treatments were compared. Results indicate the plant hormone, cytokinine (CK) foliar treatment, increased evapotranspiration rate in both tested plants. The Hg uptake and translocation in both tested plants increased with simultaneous addition of CK and TS treatments. B. juncea was the most effective in Hg uptake. Application of CK to plants grown in TS-treated soil lead to an increase in Hg concentration of 232% in shoots and 39% in roots with respect to control. While H. annuus gave a better response in plant biomass production, the application of CK to plants grown in TS-treated soil lead to

  12. Thermal cycling reliability of indirect hybrid HgCdTe infrared detectors

    Science.gov (United States)

    Chen, Xing; He, Kai; Wang, Jian-xin; Zhang, Qin-yao

    2013-09-01

    Thermal cycling reliability is one of the most important issues whether the HgCdTe infrared focal plane array detectors can be applied to both military and civil fields. In this paper, a 3D finite element model for indirect hybrid HgCdTe infrared detectors is established. The thermal stress distribution and thermally induced warpage of the detector assembly as a function of the distance between the detector chip and Si-ROIC, the thickness and the materials properties of electrical lead board in cryogenic temperature are analyzed. The results show that all these parameters have influences on the thermal stress distribution and warpage of the detector assembly, especially the coefficient of thermal expansion(CTE) of electrical lead board. The thermal stress and warpage in the assembly can be avoided or minimized by choosing the appropriate electrical lead board. Additionally, the warpage of some indirect hybrid detectors assembly samples is measured in experiment. The experimental results are in good agreement with the simulation results, which verifies that the results are calculated by finite element method are reasonable.

  13. Effect of doping on electronic properties of HgSe

    Science.gov (United States)

    Nag, Abhinav; Sastri, O. S. K. S.; Kumar, Jagdish

    2016-05-01

    First principle study of electronic properties of pure and doped HgSe have been performed using all electron Full Potential Linearized Augmented Plane Wave (FP-LAPW) method using ELK code. The electronic exchange and co-relations are considered using Generalized Gradient Approach (GGA). Lattice parameter, Density of States (DOS) and Band structure calculations have been performed. The total energy curve (Energy vs Lattice parameter), DOS and band structure calculations are in good agreement with the experimental values and those obtained using other DFT codes. The doped material is studied within the Virtual Crystal Approximation (VCA) with doping levels of 10% to 25% of electrons (hole) per unit cell. Results predict zero band gap in undopedHgSe and bands meet at Fermi level near the symmetry point D. For doped HgSe, we found that by electron (hole) doping, the point where conduction and valence bands meet can be shifted below (above) the fermi level.

  14. Characterization studies of purified HgI{sub 2} precursors

    Energy Technology Data Exchange (ETDEWEB)

    Schieber, M. E-mail: Schieber@vms.huji.ac.il; Zuck, A.; Sanguinetti, S.; Montalti, M.; Braiman, M.; Melekhov, L.; Nissenbaum, J.; Grilli, E.; Guzzi, M.; Turchetta, R.; Dulinski, W.; Husson, D.; Riester, J.L

    1999-06-01

    The ability of HgI{sub 2} powders, used as precursors in mercuric iodide crystal growth, to produce high-quality detectors may be predicted by non-destructive methods like photoluminescence. In fact, it is possible to correlate the presence and the intensity ratio of specific bands in the photoluminescence spectrum of a HgI{sub 2} crystal to its impurity content and stoichiometry. These quantities determine the detector grade that may be achieved using that starting material. Nine different HgI{sub 2} precursors, obtained by different purification methods, have been characterized. The lowest impurity content is achieved via poly-ethylene treatment, which gives also a powder of relatively good stoichiometric quality.

  15. [Experimental Research of Hg (II) Removal from Aqueous Solutions of HgCl2 with Nano-TiO2].

    Science.gov (United States)

    Zhou, Xiong; Zhang, Jin-yang; Wang, Ding-yong; Qin, Cai-qing; Xu, Feng; Luo Cheng-zhong; Yang, Xi

    2016-01-15

    Mercury removal from aqueous solutions of HgCl2 was studied by indoor simulation experiments, and the effects of three different diameter of particles of Nano-TiO2 ( Nano-Titanium Dioxide) at different dosage, pH, adsorption time and the initial concentration of Hg2+ on the mercury adsorption from simulated wastewater were investigated. The single factor experiments showed that the optimal conditions were: 7.5 g x L(-1) of 5 nm TiO2 or 2.0 g x L(-1) of 100 nm TiO2, pH 8.0, initial concentration of Hg2+ 15 x mg x L(-1) adsorption time 5 min, and under these conditions the adsorption rates reached 99.5% and 99.3%, relatively. When the content of 25 nm TiO2 was 10 g x L(-1), and the other conditions were pH 8.0, initial concentration of Hg2+ 15 mg x L(-1), adsorption time 60 min, the adsorption rate was 62.8%. The Hg(II) removal effects of the TiO2 particles with different diameters followed the order of 100 nm TiO2 > 5 nm TiO2 > 25 nm TiO2. Component adsorption results showed that the 5 nm TiO2 component adsorption effect was superior to its single adsorption effect, while there was little difference between 100 nm TiO2 component adsorption effect and its single adsorption effect. The results of orthogonal experiments indicated that the influencing factors of the adsorption rate followed the order of pH > the initial concentration of Hg2+ > time > dosage. The optimal experiment scheme was: pH 8.0, a dosage of 100 nm Nano-TiO2 of 2.0 g x L(-1) an initial Hg2+ concentration of 25 mg x L(-1) and adsorption time of 10 min. Under the experimental conditions, the maximum adsorption rate reached 99.9%, at the same time, the equilibrium concentration of Hg(II) was 0.033 mg x L(-1) mercury emissions limits. In addition, the maximum adsorptive capacity was 26.95 mg x g(-1). The adsorption isotherm was in line with the Langmuir isotherm equation, indicating that the Hg(II) uptake by 100 nm Nano-TiO2 was typical monolayer adsorption. PMID:27078961

  16. Colloidally prepared CdHgTe and HgTe quantum dots with strong near-infrared luminescence

    Energy Technology Data Exchange (ETDEWEB)

    Rogach, A.L.; Kornowski, A.; Eychmueller, A.; Weller, H. [Hamburg Univ. (Germany). Inst. fuer Physikalische Chemie; Harrison, M.T.; Kershaw, S.V.; Burt, M.G. [Corning Research Centre, Suffolk (United Kingdom)

    2001-03-01

    Several series of CdHgTe composite nanocrystals were prepared using thiol-capped CdTe nanocrystal precursors to which subsequent layers of HgTe and CdTe were added. The position of the 'excitonic' photoluminescence peak measured at room temperature was red-shifted to the near infrared to give emission wavelengths ranging from 800 to 1100 nm depending on the quantum dot composition, with quantum efficiency (QE) significantly increased over the pure CdTe material (QE up to around 40%). Thiol-capped HgTe nanocrystals synthesized in aqueous solution show a broad photoluminescence with a QE of {proportional_to}50%. It has been shown using D{sub 2}O as a solvent that by varying the synthesis conditions it is possible to tune the luminescence of HgTe quantum dots to the desired wavelength in the range of 900-2000 nm. HgTe nanocrystals passivated at the surface with a thick CdS layer have been shown to be much more robust towards heating and ''aging'' of the optical properties. (orig.)

  17. MBE HgCdTe for HDVIP Devices: Horizontal Integration in the US HgCdTe FPA Industry

    Science.gov (United States)

    Aqariden, F.; Elsworth, J.; Zhao, J.; Grein, C. H.; Sivananthan, S.

    2012-10-01

    Molecular beam epitaxy (MBE) growth of HgCdTe offers the possibility of fabricating multilayer device structures with an almost unlimited choice of infrared sensor designs for focal-plane array (FPA) fabrication. HgCdTe offers two major advantages that explain its dominance in the infrared photon detector marketplace. The thermal generation rate per unit volume of the material is lower and the quantum efficiency for photon absorption in the infrared is higher in HgCdTe than in any competing material—it yields devices with quantum efficiencies as high as 0.99. Recently, EPIR Technologies and DRS Infrared Technologies agreed to collaborate and examine: (i) the feasibility of employing MBE HgCdTe in the fabrication of high-density vertically interconnected photodiodes (HDVIPs), which are usually fabricated with liquid-phase epitaxy material, and (ii) the potential benefits of horizontal integration, with EPIR supplying the MBE materials to DRS for device and array fabrication. The team designed and developed passivation-absorber-passivation structures that are heavily used by DRS. This paper provides an overview of the characteristics of HDVIP devices and arrays fabricated from MBE HgCdTe and the anticipated advantages of horizontal integration in the industry. Material growth, device fabrication, and test results are presented.

  18. Mercury (Hg) burden in children: the impact of dental amalgam.

    Science.gov (United States)

    Al-Saleh, Iman; Al-Sedairi, Al Anoud

    2011-07-15

    The risks and benefits of using mercury (Hg) in dental amalgam have long been debated. This study was designed to estimate Hg body burden and its association with dental amalgam fillings in 182 children (ages: 5-15 years) living in Taif City. Hg was measured in urine (UHg), hair (HHg) and toenails (NHg) by the Atomic Absorption Spectrophotometer with Vapor Generator Accessory system. Urinary Hg levels were calculated as both micrograms per gram creatinine (μg/g creatinine) and micrograms per liter (μg/L). We found that children with amalgam fillings (N=106) had significantly higher UHg-C levels than children without (N=76), with means of 3.763 μg/g creatinine versus 3.457 μg/g creatinine, respectively (P=0.019). The results were similar for UHg (P=0.01). A similar pattern was also seen for HHg, with means of 0.614 μg/g (N=97) for children with amalgam versus 0.242 μg/g (N=74) for those without amalgam fillings (P=0). Although the mean NHg was higher in children without amalgam (0.222 μg/g, N=61) versus those with (0.163 μg/g, N=101), the relationship was not significant (P=0.069). After adjusting for many confounders, the multiple logistic regression model revealed that the levels of UHg-C and HHg were 2.047 and 5.396 times higher, respectively, in children with dental amalgam compared to those without (Pdental amalgam fillings (P=0.003). Despite the controversy surrounding the health impact of dental amalgam, this study showed some evidence that amalgam-associated Hg exposure might be related with symptoms of oral health, such as aphthous ulcer, white patches, and a burning-mouth sensation. Further studies are needed to reproduce these findings. The present study showed that significant numbers of children with or without amalgam had Hg levels exceeding the acceptable reference limits. The detrimental neurobehavioral and/or nephrotoxic effects of such an increased Hg on children should be a cause of concern, and further investigation is warranted. Our

  19. HgMn Stars as apparent X-ray emitters

    OpenAIRE

    Hubrig, S.; Berghoefer, W.; Mathys, G.

    1998-01-01

    In the ROSAT all-sky survey 11 HgMn stars were detected as soft X-ray emitters (Berghoefer, Schmitt & Cassinelli 1996). Prior to ROSAT, X-ray observations with the Einstein Observatory had suggested that stars in the spectral range B5-A7 are devoid of X-ray emission. Since there is no X-ray emitting mechanism available for these stars (also not for HgMn stars), the usual argument in the case of an X-ray detected star of this spectral type is the existence of an unseen low-mass companion which...

  20. Preventing Hg Transference from Soil to Terrestrial Food Chain

    Institute of Scientific and Technical Information of China (English)

    QINGCHANG-LE; MOUSHU-SEN

    1993-01-01

    Hg in acid soil could be activited by liming and become available to plant,if excessive or insufficient amount of line was applied.The changes of Hg activity in acid soil with different rates of CaCO3 amendment were studied by a pot experiment.To predict the adequate amount of lime application,a simple method using the pH(EDTA) as an indicator was suggested.The suitable range of lime application was the amount of lime addition when the pH of soil-EDTA system was raised to 4.0-4.3.

  1. Transuranium elements

    International Nuclear Information System (INIS)

    In this paper, the authors introduce this volume of historical and research papers on the transuranium elements by reviewing the period of discovery of elements 93 and beyond. Then the authors highlight the research achievements that focus on the unique properties of the 5f elements. Finally, the authors outline the technology and applications of transuranium elements and their radiobiology

  2. Low Temperature, Rapid Thermal Cycle Annealing of HgCdTe Grown on CdTe/Si

    Science.gov (United States)

    Simingalam, Sina; Brill, Gregory; Wijewarnasuriya, Priyalal; Rao, Mulpuri V.

    2015-05-01

    The HgCdTe(MCT) grown on CdTe/Si substrate has a high dislocation density due to lattice mismatch. Thermal cycle annealing (TCA) is effective in reducing the dislocation density. The TCA at high temperatures results in inter-diffusion of the constituent elements across the MCT/CdTe interface. In this study, we observed a reduction in dislocation density with good surface morphology due to proper design of the TCA system, low annealing temperature, and large number of annealing cycles. The ampoule containing the samples is placed in direct contact with the graphite heating tube which helps in increasing the heating and cooling rates of the annealing cycle. To maintain Hg overpressure, Hg is placed in the sample holder, instead of in the ampoule to avoid Hg condensation. The best results were obtained by cycling the annealing temperature between 290°C and 350°C. Anneals were performed by using 32, 64, 128 and 256 cycles. We obtained an etch pit density (EPD) as low as 1 × 106 cm-2. Lower EPD was not achieved either by increasing annealing temperature or number of annealing cycles. Through secondary ion mass spectroscopy analysis, we observed very little inter-diffusion of Cd across the MCT/CdTe interface for the 128 cycle annealing. These results show promise in bridging the gap in the device performance between the MCT material grown on CdTe/Si and CdZnTe substrates.

  3. Simulation and evaluation of elemental mercury concentration increase in flue gas across a wet scrubber.

    Science.gov (United States)

    Chang, John C S; Ghorishi, S Behrooz

    2003-12-15

    Experimental data from a laboratory-scale wet scrubber simulator confirmed that oxidized mercury, Hg2+, can be reduced by aqueous S(IV) (sulfite and/or bisulfite) species and results in elemental mercury (HgO) emissions under typical wet FGD scrubber conditions. The S(IV)-induced Hg2+ reduction and Hg0 emission mechanism can be described by a model which assumes that only a fraction of the Hg2+ can be reduced, and the rate-controlling step of the overall process is a first-order reaction involving the Hg-S(IV) complexes. Experimental data and model simulations predict that the Hg2+ in the flue gas can cause rapid increase of Hg0 concentration in the flue gas across a FGD scrubber. Forced oxidation can enhance Hg2+ reduction and Hg0 emission by decreasing the S(IV) concentration in the scrubbing liquor. The model predictions also indicate that flue gas Hg0 increase across a wet FGD scrubber can be reduced by decreasing the pH, increasing S(IV) concentration, and lowering the temperature. PMID:14717192

  4. Formation of Soluble Mercury Oxide Coatings: Transformation of Elemental Mercury in Soils.

    Science.gov (United States)

    Miller, Carrie L; Watson, David B; Lester, Brian P; Howe, Jane Y; Phillips, Debra H; He, Feng; Liang, Liyuan; Pierce, Eric M

    2015-10-20

    The impact of mercury (Hg) on human and ecological health has been known for decades. Although a treaty signed in 2013 by 147 nations regulates future large-scale mercury emissions, legacy Hg contamination exists worldwide and small-scale releases will continue. The fate of elemental mercury, Hg(0), lost to the subsurface and its potential chemical transformation that can lead to changes in speciation and mobility are poorly understood. Here, we show that Hg(0) beads interact with soil or manganese oxide solids and X-ray spectroscopic analysis indicates that the soluble mercury coatings are HgO. Dissolution studies show that, after reacting with a composite soil, >20 times more Hg is released into water from the coated beads than from a pure liquid mercury bead. An even larger, >700 times, release occurs from coated Hg(0) beads that have been reacted with manganese oxide, suggesting that manganese oxides are involved in the transformation of the Hg(0) beads and creation of the soluble mercury coatings. Although the coatings may inhibit Hg(0) evaporation, the high solubility of the coatings can enhance Hg(II) migration away from the Hg(0)-spill site and result in potential changes in mercury speciation in the soil and increased mercury mobility.

  5. Formation of Soluble Mercury Oxide Coatings: Transformation of Elemental Mercury in Soils.

    Science.gov (United States)

    Miller, Carrie L; Watson, David B; Lester, Brian P; Howe, Jane Y; Phillips, Debra H; He, Feng; Liang, Liyuan; Pierce, Eric M

    2015-10-20

    The impact of mercury (Hg) on human and ecological health has been known for decades. Although a treaty signed in 2013 by 147 nations regulates future large-scale mercury emissions, legacy Hg contamination exists worldwide and small-scale releases will continue. The fate of elemental mercury, Hg(0), lost to the subsurface and its potential chemical transformation that can lead to changes in speciation and mobility are poorly understood. Here, we show that Hg(0) beads interact with soil or manganese oxide solids and X-ray spectroscopic analysis indicates that the soluble mercury coatings are HgO. Dissolution studies show that, after reacting with a composite soil, >20 times more Hg is released into water from the coated beads than from a pure liquid mercury bead. An even larger, >700 times, release occurs from coated Hg(0) beads that have been reacted with manganese oxide, suggesting that manganese oxides are involved in the transformation of the Hg(0) beads and creation of the soluble mercury coatings. Although the coatings may inhibit Hg(0) evaporation, the high solubility of the coatings can enhance Hg(II) migration away from the Hg(0)-spill site and result in potential changes in mercury speciation in the soil and increased mercury mobility. PMID:26389816

  6. Electronic structures of HgTe and CdTe surfaces and HgTe/CdTe interfaces

    Science.gov (United States)

    Schick, J. T.; Bose, S. M.; Chen, A.-B.

    1989-01-01

    A Green's-function method has been used to study the surface and interface electronic structures of the II-VI compounds HgTe and CdTe. Localized surface and resonance states near the cation-terminated (100) surface of CdTe and the anion-terminated surface of HgTe have been found for the ideal surfaces. The energies and strengths of these surface states are altered by surface perturbations. The bulk states near the surface are drastically modified by the creation of the surface, but the band gaps remain unchanged. Numerical evaluation of the local densities of states at the Gamma and J points shows that, at the (100) interface of HgTe/CdTe, the previously observed surface states are no longer present. However, in the interface region, bulk states of one material penetrate some distance into the other material.

  7. Synthesis and characterization of complexes of monoacetylferrocene-4-phenyl thiosemicarbazone with UO22+, Hg2+, Ni2+ or Zn2+ ions

    International Nuclear Information System (INIS)

    Complexes have been synthesized with monoacetylferrocene-4-phenyl thiosemicarbazone (L) combining with UO22+, Hg2+, Ni2+ or Zn2+ ions and characterized through elemental analysis, IR spectrum, UV spectrum and 1HNMR spectrum. The thermal stability and molar conductance have been studied. It shows that L coordinates to the metal ion in a Keto form and is a bidentate ligand

  8. Determination of As, Cd, Cr, Cu, Hg, Sb and Se concentrations by radiochemical neutron activation analysis in different Brazilian regional diets

    International Nuclear Information System (INIS)

    Radiochemical separation procedures developed for the determination of seven elements: As, Cd, Cr, Cu, Hg, Sb and Se in different Brazilian regional diets are described. In the case of the elements As, Hg, Sb and Se, the procedure was based on retention in inorganic exchanger TFO (tin dioxide) and determination of Hg by extraction with Ni(DDC)2. For determination of Cd, Cr, Cu and Se the procedure chosen was based on retention in inorganic exchanger HMD (hydrated manganese dioxide) and extraction of Cu and Cd as diethyldithiocarbamate compounds. The accuracy and precision of the methods studied were tested by means of analyses of different reference materials-Due to the lack of data on trace element levels in Brazilian foodstuffs and diets, these methods were applied to determination of these elements in different Brazilian regional diets. These s were supplied by the Food and Experimental Nutrition Department of the Faculty of Pharmaceutical Science, University of Sao Paulo. The daily intake values for these diets are presented for As, Cd, Cr, Cu, Hg, Sb and Se. (author) 21 refs.; 6 tabs

  9. Interpretation of the vacancy-ordering controlled growth morphology of Hg{sub 5}In{sub 2}Te{sub 8} precipitates in Hg{sub 3}In{sub 2}Te{sub 6} single crystals by TEM observation and crystallographic calculation

    Energy Technology Data Exchange (ETDEWEB)

    Sun, Jie [State Key Laboratory of Solidification Processing, Northwestern Polytechnical University, 127 Youyi Road, Xi’an (China); School of Chemical and Biomolecular Engineering, The University of Sydney, NSW 2006 (Australia); Australian Centre for Microscopy and Microanalysis, The University of Sydney, NSW 2006 (Australia); Fu, Li, E-mail: fuli@nwpu.edu.cn [State Key Laboratory of Solidification Processing, Northwestern Polytechnical University, 127 Youyi Road, Xi’an (China); Liu, Hongwei [Australian Centre for Microscopy and Microanalysis, The University of Sydney, NSW 2006 (Australia); Ringer, S.P. [Australian Centre for Microscopy and Microanalysis, The University of Sydney, NSW 2006 (Australia); School of Aerospace, Mechanical and Mechatronic Engineering, The University of Sydney, NSW 2006 (Australia); Liu, Zongwen, E-mail: zongwen.liu@sydney.edu.au [School of Chemical and Biomolecular Engineering, The University of Sydney, NSW 2006 (Australia)

    2015-02-15

    Graphical abstract: The growth morphology and detailed crystallography of Hg{sub 5}In{sub 2}Te{sub 8} precipitates in Hg{sub 3}In{sub 2}Te{sub 6} matrix to has been interpreted by means of transmission electron microscopy and invariant element deformation model. Three crystallographic equivalent variants of Hg{sub 5}In{sub 2}Te{sub 8} precipitates in Hg{sub 3}In{sub 2}Te{sub 6} matrix were found to have different growth directions and habit planes. Such growth morphology is fully attributed to the lattice shrinkage induced by vacancy ordering under high temperature in Hg{sub 5}In{sub 2}Te{sub 8}. Through near coincident site lattice and invariant strain calculation, the morphology and crystallographic features of the precipitate has been successfully interpreted. - Highlights: • The growth morphology of Hg{sub 5}In{sub 2}Te{sub 8} precipitates in Hg{sub 3}In{sub 2}Te{sub 6} was observed by TEM. • Near-CSL calculation show 0.7577% lattice shrinkage of Hg{sub 5}In{sub 2}Te{sub 8} at high temperature. • All the involved factors have inverse relationship with the move speed of interface. • The calculated crystallography features of Hg{sub 5}In{sub 2}Te{sub 8} agree well with the TEM results. - Abstract: Generally, the crystal growth morphology in liquid or vapor was controlled by chemical potential, while that in solid solute was restricted by 3D strain matching between matrix and secondary phase. It is already known that the growth and evolution of the morphology of secondary phase during the solid phase transformation are highly determined by the variation of interface energy induced by lattice mismatch. In this work, the growth morphology and crystallography of Hg{sub 5}In{sub 2}Te{sub 8} precipitates in Hg{sub 3}In{sub 2}Te{sub 6} matrix were investigated by means of transmission electron microscopy (TEM). It was found that the growth of Hg{sub 5}In{sub 2}Te{sub 8} precipitates displayed an unusual growth morphology which contain three crystallographically

  10. Preparation and Hg~(2+) Adsorption of N-thioacyl Thioglycolic Acid Functionalized Triethylenetetramine Crosslinked PVC Resin%N-硫代酰基硫乙酸功能化三乙撑四胺交联PVC树脂的制备及对Hg~(2+)的吸附

    Institute of Scientific and Technical Information of China (English)

    刘春萍; 纪春暖; 蒙延峰; 吕菊波; 孙琳

    2009-01-01

    A novel acidic N-thioacyl thioglycolic acid functionalized triethylentetramine crosslinked PVC resin was preparated from PVC, triethylenetetramine, CS_2 and ClCH_2COONa and characterized by FTIR and elemental analysis. Adsorption properties of the resin for Hg~(2+) were investigated under different conditions such as pH, temperature, contact time and the initial concentration of Hg~(2+). The results show that the adsorption of the resin for Hg~(2+) could rapidly reach balance, and it displayed a higher capacity when pH was about 2.0. The adsorption capacity of the resin for Hg~(2+) reached 3.330 mmol/g at 35 ℃ and 17.66 mmol/L Hg~(2+). The adsorption process was fitted to Langmuir and Freundlich isotherms in the studied concentration range. The loaded resin with Hg~(2+) was regenerated in an efficiency of 99.2% via 0.2 mol/L HNO_3-10% thiourea.%以聚氯乙烯为原料依次与四乙烯五胺、CS_2和ClCH_2COONa反应合成了一种新的含N、O、S的N-硫代酰基硫乙酸功能化三乙撑四胺交联聚氯乙烯螯合树脂,树脂结构经红外分析和元素分析表征. 探讨了在不同pH值、Hg~(2+)初始浓度、吸附温度和时间等条件下合成树脂对Hg~(2+)的吸附性能. 结果表明,螯合树脂对Hg~(2+)有较快的吸附速率,pH值约为2.0时,树脂对Hg~(2+)的吸附效果最好,随温度升高吸附量逐渐增大. 温度在35 ℃、Hg~(2+)起始浓度为17.66 mmol/L时,树脂对Hg~(2+)的吸附量可达3.330 mmol/g. 树脂对Hg~(2+)的吸附符合Langmuir和Freundlich等温式. 用0.2 mol/L HNO3-10%硫脲对吸附后的树脂进行洗脱,脱附率达99.20%.

  11. Comparison of the characteristics and mechanisms of Hg(II) sorption by biochars and activated carbon.

    Science.gov (United States)

    Xu, Xiaoyun; Schierz, Ariette; Xu, Nan; Cao, Xinde

    2016-02-01

    Two biochars were produced from bagasse and hickory chips (referred to as BB and HCB, respectively) and evaluated for their sorption ability of Hg(II) in aqueous solution. A commercial activated carbon (AC) which is commonly used for Hg(II) removal was included for comparison. Both biochars showed higher sorption capacities than AC, following the trend of BB>HCB>AC. The sorption of Hg(II) by BB and AC was mainly attributed to the formation of (COO)2Hg(II) and (O)2Hg(II). As a result, the adsorption capacity of Hg(II) by BB decreased 17.6% and 37.6% after COOH and OH were blocked, respectively and that of Hg(II) by AC decreased 6.63% and 62.2% for COOH and OH hindered, respectively. However, blocking the function groups had little effect on the Hg removal by HCB since sorption of Hg(II) by HCB was mainly resulted from the π electrons of CC and CO induced Hg-π binding. Further X-ray photoelectron spectroscopy analysis indicated the possibility of reduction of the Hg(II) to Hg(I) by phenol groups or π electrons during the removal of Hg(II) by both biochars. In conclusion, biochar is more effective than activated carbon in removing Hg(II) and there exists a high potential that biochar can be a substitute of activated carbon for removal of Hg(II) from wastewater.

  12. Comparison of the characteristics and mechanisms of Hg(II) sorption by biochars and activated carbon.

    Science.gov (United States)

    Xu, Xiaoyun; Schierz, Ariette; Xu, Nan; Cao, Xinde

    2016-02-01

    Two biochars were produced from bagasse and hickory chips (referred to as BB and HCB, respectively) and evaluated for their sorption ability of Hg(II) in aqueous solution. A commercial activated carbon (AC) which is commonly used for Hg(II) removal was included for comparison. Both biochars showed higher sorption capacities than AC, following the trend of BB>HCB>AC. The sorption of Hg(II) by BB and AC was mainly attributed to the formation of (COO)2Hg(II) and (O)2Hg(II). As a result, the adsorption capacity of Hg(II) by BB decreased 17.6% and 37.6% after COOH and OH were blocked, respectively and that of Hg(II) by AC decreased 6.63% and 62.2% for COOH and OH hindered, respectively. However, blocking the function groups had little effect on the Hg removal by HCB since sorption of Hg(II) by HCB was mainly resulted from the π electrons of CC and CO induced Hg-π binding. Further X-ray photoelectron spectroscopy analysis indicated the possibility of reduction of the Hg(II) to Hg(I) by phenol groups or π electrons during the removal of Hg(II) by both biochars. In conclusion, biochar is more effective than activated carbon in removing Hg(II) and there exists a high potential that biochar can be a substitute of activated carbon for removal of Hg(II) from wastewater. PMID:26520810

  13. Experimental study of 199Hg spin anti-relaxation coatings

    CERN Document Server

    Chowdhuri, Z; Horras, M; Kirch, K; Krempel, J; Lauss, B; Mtchedlishvili, A; Rebreyend, D; Roccia, S; Schmidt-Wellenburg, P; Zsigmond, G

    2013-01-01

    We report on a comparison of spin relaxation rates in a $^{199}$Hg magnetometer using different wall coatings. A compact mercury magnetometer was built for this purpose. Glass cells coated with fluorinated materials show longer spin coherence times than if coated with their hydrogenated homologues. The longest spin relaxation time of the mercury vapor was measured with a fluorinated paraffin wall coating.

  14. Use of HgI2 as gamma radiation detector

    International Nuclear Information System (INIS)

    The Mercuric Iodide (HgI2) has become one of the most promising room temperature semiconductors for the construction of X and gamma radiation detectors. The classical methods of spectroscopy have not demonstrated to achieve optimum results with HgI2 detectors, mainly due to its particular carrier transport properties. Several alternative spectroscopic methods developed in the last ten years are presented and commented, selecting for a complete study one of them: 'The Partial Charge Collection Method'. The transport properties of the carriers generated by the radiation in the detector is specially important for understanding the spectroscopic behaviour of the HgI2 detectors. For a rigorous characterization of this transport, it has been studied a digital technique for the analysis of the electric pulses produced by the radiation. Theoretically, it has been developed a Monte Carlo simulation of the radiation detection and the electronic signal treatment processes with these detectors in the energy range of 60-1300 KeV. These codes are applied to the study of the The Partial Charge Collection Method and its comparison with gaussian methods. Experimentally, this digital techniques is used for the study of the transport properties of thin HgI2 detectors. Special interest is given to the contribution of the slower carriers, the holes, obtaining some consequent of spectroscopic interest. Finally, it is presented the results obtained with the first detectors grown and mounted in CIEMAT with own technology. (author). 129 ref

  15. Thermodynamic investigations of CdTe-HgTe solid solutions

    Energy Technology Data Exchange (ETDEWEB)

    Nasar, A.; Shamsuddin, M. (Dept. of Metallurgical Engineering, Banaras Hindu Univ., Varanasi (India))

    1991-08-10

    The activity of CdTe in pseudobinary CdTe-HgTe solid solution (with CdTe added in 10 mol.% increments) has been determined in the temperature range 735-840 K by an electrochemical technique using LiCl-KCl+5 wt.% CdCl{sub 2} as the molten salt electrolyte. The activity of HgTe has been calculated by Gibbs-Duhem integration using the {alpha} function. From the e.m.f. values measured at different temperatures, various partial and excess thermodynamic quantities, namely {Delta}anti G{sup M}{sub CdTe}, {Delta}anti H{sup M}{sub CdTe}, {Delta}anti S{sup XS}{sub CdTe}, {Delta}anti G{sup XS}{sub CdTe} and {Delta}anti S{sup XS}{sub CdTe}, have been obtained. The corresponding thermodynamic parameters for HgTe have also been computed. The integral molar properties of the solid solutions have been estimated from the partial quantities of the two components, CdTe and HgTe. (orig.).

  16. Decay from the superdeformed bands in {sup 194}Hg

    Energy Technology Data Exchange (ETDEWEB)

    Henry, R.G.; Khoo, T.L.; Carpenter, M.P. [and others

    1995-08-01

    Superdeformed bands in {sup 194}H g were studied using the early implementation of Gammasphere. The response functions for the Ge detectors were measured for the first time as part of this experiment. Experiments were performed with both a backed target (where the residue stopped in the Au backing) and a thin target (where the residue recoiled into vacuum). This will permit measurements of the decay times of the quasicontinuum {gamma}rays. The spectrum in coincidence with the yrast SD band in {sup 194}Hg reveals the same features as found in the quasicontinuum structure in {sup 192}Hg. These features include: statistical {gamma}rays feeding the SD band, a pronounced E2 peak from transitions feeding the SD band, a Ml/E2 bump at low energies that is associated with the last stages of feeding of the superdeformed band, and a quasicontinuous distribution from {gamma}rays linking SD and normal states, including a sizable clustering of strength around 1.7 MeV. The remarkable similarity of the spectra coincident with SD bands in {sup 192,194}Hg provides additional support for a statistical process for decay out of the SD states. This similarity contrasts with differences observed in the spectrum coincident with the SD band in the odd-even {sup 191}Hg, confirming the predictions about the role of pairing (in normal states) in influencing the shape of the decay-out spectrum.

  17. 40 CFR 60.4142 - Hg allowance allocations.

    Science.gov (United States)

    2010-07-01

    ... produced by any associated heat recovery steam generator during the control period divided by 0.8, and with... paragraph (b) of this section for each Hg Budget unit will be: (i) For units commencing operation before... paragraph (a)(1)(i)(A) or (B) of this section, multiplied by 1.0. (ii) For units commencing operation on...

  18. Seasonal Survey of Contaminants (Cd and Hg) and Micronutrients (Cu and Zn) in Edible Tissues of Cephalopods from Tunisia: Assessment of Risk and Nutritional Benefits

    OpenAIRE

    Rjeibi, Moncef; Metian, Marc; Hajji, Tarek; Guyot, Thierry; Rafika, Ben Chaouacha-Chekir; Bustamante, Paco

    2015-01-01

    International audience Concentrations of cadmium (Cd), copper (Cu), mercury (Hg) and zinc (Zn) were determined by atomic absorption spectrophotometry in the muscle tissues (arms and mantle) of three commercial cephalopods (Loligo vulgaris, Octopus vulgaris and Sepia officinalis) caught in three different Tunisian coastal regions. The highest concentrations found correspond to the essential elements Cu and Zn. Octopuses and cuttlefish showed the highest levels of those elements while squid ...

  19. Trace enrichment with activated carbon and determination of Ni, Hg, Sn and Cd using diethyldithiocarbamate as complexant by atomic emission spectrography (AES)

    International Nuclear Information System (INIS)

    A methods has been developed for the preconcentration and determination of trace amounts of Hg, Ni, Sn and Cd in aqueous solutions. The complexes of these elements with sodium diethyl dithiocarbamate were adsorbed on activated charcoal and determined by atomic emission spectrography d-c arc technique. Factors which affect the quantitative recovery of the microamounts of the elements were optimised. Pd was used as an internal standard. The detection limits ranged from 0.01 to 0.05 ppm. (author)

  20. History of HgTe-based photodetectors in Poland

    Science.gov (United States)

    Rogalski, A.

    2010-09-01

    In Poland, the HgCdTe studies began in 1960 at the Institute of Physics, Warsaw University. The material processing laboratory was created by Giriat and later by Dziuba, Gałązka, and others. Bridgman technique with sealed thick wall quartz ampoules was used to grow material suitable for research and experimental devices. Among the first papers published in 1961 and 1963 there were the Polish works devoted to preparation, doping, and electrical properties of HgCdTe. Infrared detector's research and development efforts in Poland were concentrated mostly on uncooled market niche. At the beginning, a modified isothermal vapour phase epitaxy has been used for research and commercial fabrication of photoconductive, photoelectromagnetic and other HgCdTe devices. Bulk growth and liquid phase epitaxy were also used. Recently, the fabrication of infrared devices relies on low temperature epitaxial technique, namely metalorganic vapour phase deposition. At present stage of development, the photoconductive and photoelectromagnetic (PEM) detectors are gradually replaced with photovoltaic devices which offer inherent advantages of no electric or magnetic bias, no heat load and no flicker noise. Potentially, photodiodes offer high performance and very fast response. However, conventional photovoltaic uncooled detectors suffer from low quantum efficiency and very low junction resistance. The problems have been solved with advanced band gap engineered architecture, multiple cell heterojunction devices connected in series, and monolithic integration of the detectors with microoptics. In final part of the paper, the Polish achievements in technology and performance of HgMnTe and HgZnTe photodetectors are presented.

  1. A GFP-based bacterial biosensor with chromosomally integrated sensing cassette for quantitative detection of Hg(II) in environment

    Institute of Scientific and Technical Information of China (English)

    Himanshu Priyadarshi; Absar Alam; Gireesh-Babu P; Rekha Das; Pankaj Kishore; Shivendra Kumar; Aparna Chaudhari

    2012-01-01

    A mercury biosensor was constructed by integrating biosensor genetic elements into E.coli JM109 chromosome in a single copy number,using the attP/attB recombination mechanism of λ phage.The genetic elements used include a regulatory protein gene (merR) along with operator/promoter (O/P) derived from the mercury resistance operon from pDU1358 plasmid of Serratia marcescens.The expression of reporter gene gfp is also controlled by merR/O/P.Integration of the construct into the chromosome was done to increase the stability and precision of the biosensor.This biosensor could detect Hg(Ⅱ) ions in the concentration range of 100-1700 mnol/L,and manifest the result as the expression of GFP.The GFP expression was significantly different (P ≤ 0.05) for each concentration of inducing Hg(Ⅱ) ions in the detection range,which reduces the chances of misinterpretation of results.A model using regression method was also derived for the quantification of the concentration of Hg(Ⅱ) in water samples.

  2. Vertical profile measurements of soil air suggest immobilization of gaseous elemental mercury in mineral soil.

    Science.gov (United States)

    Obrist, Daniel; Pokharel, Ashok K; Moore, Christopher

    2014-02-18

    Evasion of gaseous elemental Hg (Hg(0)g) from soil surfaces is an important source of atmospheric Hg, but the volatility and solid-gas phase partitioning of Hg(0) within soils is poorly understood. We developed a novel system to continuously measure Hg(0)g concentrations in soil pores at multiple depths and locations, and present a total of 297 days of measurements spanning 14 months in two forests in the Sierra Nevada mountains, California, U.S. Temporal patterns showed consistent pore Hg(0)g concentrations below levels measured in the atmosphere (termed Hg(0)g immobilization), ranging from 66 to 94% below atmospheric concentrations throughout multiple seasons. The lowest pore Hg(0)g concentrations were observed in the deepest soil layers (40 cm), but significant immobilization was already present in the top 7 cm. In the absence of sinks or sources, pore Hg(0)g levels would be in equilibrium with atmospheric concentrations due to the porous nature of the soil matrix and gas diffusion. Therefore, we explain decreases in pore Hg(0)g in mineral soils below atmospheric concentrations--or below levels found in upper soils as observed in previous studies--with the presence of an Hg(0)g sink in mineral soils possibly related to Hg(0)g oxidation or other processes such as sorption or dissolution in soil water. Surface chamber measurements showing daytime Hg(0)g emissions and nighttime Hg(0)g deposition indicate that near-surface layers likely dominate net atmospheric Hg(0)g exchange resulting in typical diurnal cycles due to photochemcial reduction at the surface and possibly Hg(0)g evasion from litter layers. In contrast, mineral soils seem to be decoupled from this surface exchange, showing consistent Hg(0)g uptake and downward redistribution--although our calculations indicate these fluxes to be minor compared to other mass fluxes. A major implication is that once Hg is incorporated into mineral soils, it may be unlikely subjected to renewed Hg(0)g re-emission from

  3. Sr(Hg{sub 1-x}Sn{sub x}){sub 4}. Variations of the EuIn{sub 4}-type structure

    Energy Technology Data Exchange (ETDEWEB)

    Wendorff, Marco; Roehr, Caroline [Freiburg Univ. (Germany). Inst. fuer Anorganische und Analytische Chemie

    2015-07-01

    Starting from the new compound SrHg{sub 2}Sn{sub 2}, which is isoelectronic and also isotypic to the indide SrIn{sub 4}, the successive substitution of Sn against the electron poor Hg has been investigated in a combined synthetic, crystallographic, and bond-theoretical study. Along the 1:4 section Sr(Hg{sub 1-x}Sn{sub x}){sub 4} a series of compounds with Sn contents x between 0.5 and 0.2 were synthesized from stoichiometric ratios of the elements. Their crystal structures, which represent three different variants of the EuIn{sub 4}-type structure, have been determined using single crystal X-ray data. The most electron rich compound SrHg{sub 2}Sn{sub 2} crystallizes in the original EuIn{sub 4}-type [monoclinic, C2/m, a = 1257.9(14), b = 490.1(4), c = 997.8(12) pm, β = 117.60(6) , Z = 4, R1 = 0.0838], with a fully ordered Hg and Sn distribution. The four atom sites form two different folded ladders with an alternating Hg/Sn distribution. Like in the KHg{sub 2}-type, the ladders are connected via six-membered rings. In between, double tubes with an internal Sn-Sn bond are connected via further Sn-Sn bonds to form sheets similar to those observed in SiAs. The most electron-poor phase SrHg{sub 3.2}Sn{sub 0.8} crystallizes in a strongly distorted variant of this structure [a = 1172.8(4), b = 497.9(2), c = 1010.0(4) pm, β = 118.860(7) , Z = 4, R1 = 0.0549]. Herein, additional Hg-Hg bonds are formed, and the open tubes are distorted into rods of edge-sharing rhombohedra resembling the structure motifs of elemental Hg. At an intermediate valence electron (v.e.) number, i.e., in SrHg{sub 2.5}Sn{sub 1.5}, an isomorphous tripled superstructure (a = 2704.4(5), b = 493.87(7), c = 1197.1(2) pm, β = 90.838(14) , Z = 12, R1 = 0.0475) occurs, where the building blocks of the two variants of the EuIn{sub 4}-type structure alternate in a 1:2 ratio. The bonding situation and the ''coloring'', i.e., the Hg/Sn distribution in the polyanionic network, are discussed

  4. Beer Law Constants and Vapor Pressures of HgI2 over HgI2(s,l)

    Science.gov (United States)

    Su, Ching-Hua; Zhu, Shen; Ramachandran, N.; Burger, A.

    2002-01-01

    Optical absorption spectra of the vapor phase over HgI2(s,l) were measured at sample temperatures between 349 and 610 K for wavelengths between 200 and 600 nm. The spectra show the samples sublimed congruently into HGI2 without any observed Hg or I2 absorption spectra. The Beer's Law constants for 15 wavelengths between 200 and 440 nm were derived. From these constants the vapor pressure of HgI2, P, was found to be a function of temperature for the liquid and the solid beta-phases: ln P(atm) = -7700/T(K) + 12.462 (liquid phase) and ln P(atm) = -10150/T(K) + 17.026 (beta-phase). The expressions match the enthalpies of vaporization and sublimation of 15.30 and 20.17 kcal/mole respectively, for the liquid and the beta-phase HgI2. The difference in the enthalpies gives an enthalpy of fusion of 4.87 kcal/mole, and the intersection of the two expressions gives a melting point of 537 K.

  5. An element

    Energy Technology Data Exchange (ETDEWEB)

    Nakamura, K.; Iidzima, K.

    1983-03-30

    An anode of a light metal is used in the element, along with an electrolyte which consists of an ether solvent and an ionogenic additive in the form of a salt of dithiocarbamic acid. The element has good discharge characteristics.

  6. Study of atomic structure of liquid Hg-In alloys using ab-initio molecular dynamics

    Energy Technology Data Exchange (ETDEWEB)

    Sharma, Nalini; Ahluwalia, P. K. [Department of Physics, Himachal Pradesh University, Shimla(HP)-171005 (India); Thakur, Anil [Department of Physics, Govt. P. G. College Solan (HP)-173212 (India)

    2015-05-15

    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. Five liquid Hg-In mixtures (Hg{sub 10}In{sub 90}, Hg{sub 30}In{sub 70}, Hg{sub 50}In{sub 50}, Hg{sub 70}In{sub 30} and Hg{sub 90}In{sub 10}) at 299K are considered. The radial distribution function g(r) and structure factor S(q) of considered alloys are compared with respective experimental results for liquid Hg (l-Hg) and (l-In). The radial distribution function g(r) shows the presence of short range order in the systems considered. Smooth curves of Bhatia-Thornton partial structure factors factor shows the presence of liquid state in the considered alloys.

  7. Study of atomic structure of liquid Hg-In alloys using ab-initio molecular dynamics

    International Nuclear Information System (INIS)

    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. Five liquid Hg-In mixtures (Hg10In90, Hg30In70, Hg50In50, Hg70In30 and Hg90In10) at 299K are considered. The radial distribution function g(r) and structure factor S(q) of considered alloys are compared with respective experimental results for liquid Hg (l-Hg) and (l-In). The radial distribution function g(r) shows the presence of short range order in the systems considered. Smooth curves of Bhatia-Thornton partial structure factors factor shows the presence of liquid state in the considered alloys

  8. Removal of Hg~0 with sodium chlorite solution and mass transfer reaction kinetics

    Institute of Scientific and Technical Information of China (English)

    2010-01-01

    The absorption behavior of Hg0 was studied experimentally by using sodium chlorite solution(NaClO2) as the absorbent in a bubble reactor.Primary influencing factors on removal efficiency of Hg0 such as NaClO2 concentration,pH,reaction temperature and the concentration of Hg0 were investigated.The results indicated that 72.91% of Hg0 removal efficiency could be achieved in acidic NaClO2 solution.The removal mechanism of Hg0 was proposed by analyzing of Hg2+ concentration in ab-sorption solution after reaction and comparing the electrode potentials between NaClO2 species and Hg2+/Hg0.The experimental results of mass transfer-reaction kinetics on oxidation of Hg0 by NaClO2 solution showed that with the increase of NaClO2 concentration and the decrease of pH value,the enhancement factor(E) and ratio of KG(Hg0)/kG(Hg0) increased and the liquid phase mass transfer resistance decreased,which is benefit to the mass transfer adsorption reaction.Although the increase of reaction temperature could improve the enhancement factor(E),but the ratio of KG(Hg0)/kG(Hg0) decreased;as a result,the liquid phase mass transfer resistance increased,therefore,the reaction rate for removal of Hg0 decreased.

  9. The Upside to Hg-DOM Associations for Water Quality: Removal of Hg from Solution Using Coagulaion with Metal-Based Salts

    Science.gov (United States)

    Henneberry, Y.; Kraus, T. E.; Fleck, J.; Krabbenhoft, D. P.; Horwath, W. R.

    2011-12-01

    This study assessed the potential use of metal-based coagulants to remove dissolved mercury (Hg) from natural waters and provides information regarding the importance of Hg associations with the dissolved organic matter (DOM) fraction and metal hydroxides. Previous research indicated coagulants were not effective at removing Hg from solution; however those studies used high concentrations of Hg, which did not reflect naturally occurring concentrations of Hg. Filtered water collected from an agricultural drain in the Sacramento-San Joaquin Delta (Delta) was treated with three industrial-grade coagulants (ferric chloride, ferric sulfate, and polyaluminum chloride) to determine their efficacy in removing both inroganic (IHg) and methylmercury (MeHg) from the water column. The Delta suffers from elevated surface water Hg concentrations and as a result is listed as an imparied water body. Coagulants removed up to 85% of DOM from solution. In the absence of DOM, all three coagulants released IHg into solution, however in the presence of DOM the coagulants removed up to 97% of IHg and 80% of MeHg. Results suggest that the removal of Hg is mediated by DOM-coagulant interactions. There was a preferential association of IHg with the more aromatic, higher molecular weight fraction of DOM but no such relationship was found for MeHg. This study offers new fundamental insights regarding large-scale removal of Hg at environmentally relevant concentrations. Research using isotopically labeled Hg is providing insight into whether coagulation can remove recently added Hg (e.g. atmospheric deposition) from solution and whether once formed, the floc can remove additional Hg from the water column.

  10. On the morphology and crystallography of Hg5In2Te8 precipitation in Hg3In2Te6

    International Nuclear Information System (INIS)

    Highlights: • The crystallography between Hg5In2Te8 and Hg3In2Te6 has been studied by TEM. • The precipitates have three variants with a 〈0 0 1〉m growth direction. • Near-CSL calculation suggests 0° or 90° mutual rotation to reach the lowest Σ value. - Abstract: Transmission electron microscopy to investigate the crystallography of Hg5In2Te8 precipitation in single crystals of Hg3In2Te6. Both the matrix and precipitate phases were confirmed to have the F4¯3m space group. The lattice constant of the precipitates was measured to be a = 1.27 nm, which is approximately double that of the matrix (0.63 nm). Three crystallographically equivalent variants of the precipitate phase were observed to exhibit a cylindrical morphology, dispersed uniformly throughout the matrix. The preferred growth direction of all three variants was along 〈0 0 1〉m. The crystallographic orientation relationship (OR) between the precipitates and matrix was found to be a cubic parallel OR. High resolution imaging indicated that the precipitate–matrix interface was fully coherent. The precipitate crystals were found to correspond to the lowest sigma value of the near coincidence site lattices when performing a 0° or 90° mutual rotation. Finally, the existence of Hg5In2Te8 precipitation was found to have a negative effect on the optical properties according to the infrared transmittance measurement. The results in this paper may have a guiding significance on the relationship between the precipitate and optical properties of similar materials

  11. Subcellular localization of several heavy metals of Hg,Cd and Pb in human liver

    Institute of Scientific and Technical Information of China (English)

    CHEN Chunying; ZHANG Peiqun; CHAI Zhifang

    2005-01-01

    Liver, as an important metabolic and detoxicological organ of human body, can be used as a good bioindicator for evaluating body burden of environmental pollutants. Its elemental contents and their chemical forms are closely related to the status of human health and disease. In this paper, the liver samples collected from normal subjects were separated to different subcellular fractions of nuclei, mitochondria, lysosome, microsome and cytosol by differential centrifugation. Then their concentrations of heavy metals of As, Pb, Cd, and Hg were determined by atomic absorption and atomic fluorescent spectroscopy. Our results show no significant difference with literature ones when comparing their gross concentrations. In the case of their subcellular distribution, the Hg concentrations are higher in mitochondrial, microsomal and cytosolic fractions; the Cd concentrations are higher in cytosolic and mitochondrial fractions, while As highest in nuclear fraction. The highest concentration of Pb is found in microsomal fraction with similarity to Fe. Mercury in liver is mainly in the form of inorganic, and methylmercury ranged from 9% to 50% with the average value of 20.9%(13.3%. These results indicate that the cellular distribution and the accumulated target organelles are quite different among these heavy metals, which suggest their various pathways and toxic mechanism in vivo.

  12. Spatial distribution of dissolved Pb,Hg,Cd,Cu and As in the Bohai Sea

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Characteristics of the spatial distribution of selected dissolved heavy metals were analyzed during large scale surveys from August 12 to 25.2003 in the Bohai Sea.Dissolved Pb was the only element with average concentrations higher than the grade-one sea water quality standard of China.The spatial distribution of dissolved Pb in surface water was similar to those of Cd,Cu and As,where the isopleths generally indicated decreasing values from the bays to the central areas.Only for Hg did the high concentrations not only appear in Liaodong Bay,Bohai Bay and Laizhou Bay,but also in the Central Area,viz.not only in inshore but also in offshore areas.Vertical distributions of dissolved Pb,Cd,Cu and As were largely uniform,while that of dissolved Hg increased with depth.We infer that the input of pollutants from land was the main influencing factor for the detected distribution patterns of dissolved heavy metals,followed by the dynamics of sea water,release from bottom sediments and biochemical processes.Comparing with historical data,average concentrations of dissolved heavy metals appear to decline in recent years.

  13. Fingerprint of different spin-orbit terms for spin transport in HgTe quantum wells

    Energy Technology Data Exchange (ETDEWEB)

    Rothe, D G; Reinthaler, R W; Liu, C-X; Hankiewicz, E M [Institut fuer Theoretische Physik und Astrophysik, Universitaet Wuerzburg, 97074 Wuerzburg (Germany); Molenkamp, L W [Physikalisches Institut (EP3), Universitaet Wuerzburg, 97074 Wuerzburg (Germany); Zhang, S-C, E-mail: hankiewicz@physik.uni-wuerzburg.d [Department of Physics, McCullough Building, Stanford University, Stanford, CA 94305-4045 (United States)

    2010-06-15

    Using k{center_dot}p theory, we derive an effective four-band model describing the physics of the typical two-dimensional topological insulator (HgTe/CdTe quantum well (QW)) in the presence of an out-of-plane (in the z-direction) inversion breaking potential and an in-plane potential. We find that up to third order in perturbation theory, only the inversion breaking potential generates new elements to the four-band Hamiltonian that are off-diagonal in spin space. When this new effective Hamiltonian is folded into an effective two-band model for the conduction (electron) or valence (heavy hole) bands, two competing terms appear: (i) a Rashba spin-orbit interaction originating from inversion breaking potential in the z-direction and (ii) an in-plane Pauli term as a consequence of the in-plane potential. Spin transport in the conduction band is further analysed within the Landauer-Buettiker formalism. We find that for asymmetrically doped HgTe QWs, the behaviour of the spin-Hall conductance is dominated by the Rashba term.

  14. Decay studies and mass measurements on isobarically pure neutron-rich Hg and Tl isotopes

    CERN Multimedia

    Schweikhard, L C; Savreux, R P; Hager, U D K; Beck, D; Blaum, K

    2007-01-01

    We propose to perform mass measurements followed by $\\beta$- and $\\gamma$-decay studies on isobarically pure beams of neutron-rich Hg and Tl isotopes, which are very poorly known due to a large contamination at ISOL-facilities with surface-ionised francium. The aim is to study the binding energies of mother Hg and Tl nuclides, as well as the energies, spins and parities of the excited and ground states in the daughter Tl and Pb isotopes. The proposed studies will address a new subsection of the nuclear chart, with Z 126, where only 9 nuclides have been observed so far. Our studies will provide valuable input for mass models and shell-model calculations: they will probe the proton hole-neutron interaction and will allow to refine the matrix elements for the two-body residual interaction. Furthermore, they also give prospects for discovering new isomeric states or even new isotopes, for which the half-lives are predicted in the minute- and second-range.\\\\ To reach the isobaric purity, the experiments will be p...

  15. Hg, Bi, Cu and Zn distribution in human teeth treated by dental amalgam measured by synchrotron microprobe

    International Nuclear Information System (INIS)

    Human teeth restored with dental amalgam were analysed by a synchrotron microprobe to evaluate the diffusion of its major constituents, Cu, Zn and Hg, throughout the tooth structures. We measured the elemental distribution inside the tooth from the root to the enamel, specially the region around the amalgam, after its total removal. Hg is present only in restored teeth and concentration profiles show strongly increased levels of this element close to the amalgam region, reaching 500 μg g-1 in one or two cases, decreasing strongly to the inner part of the tooth. Pb concentration profiles do not seem to be affected by metallic amalgam. Very high concentrations of Bi were found in one of the restored teeth, reaching more than 2000 μg g-1, decreasing sharply to the outer regions. The distribution of Mn, Fe, Cu and Zn was also determined in order to evaluate elemental influences by amalgam components. No significant changes in elemental concentrations were detected for Mn and Fe between healthy and restored teeth. However, the levels of Zn and Cu are increased in restored teeth. An X-ray fluorescence set-up with microprobe capabilities, 100 μm of spatial resolution and an energy of 18 keV, installed at LURE synchrotron (France) was used

  16. Hg, Bi, Cu and Zn distribution in human teeth treated by dental amalgam measured by synchrotron microprobe

    Science.gov (United States)

    Carvalho, M. L.; Marques, J. P.; Brito, J.; Casaca, C.; Cunha, A. S.

    2002-11-01

    Human teeth restored with dental amalgam were analysed by a synchrotron microprobe to evaluate the diffusion of its major constituents, Cu, Zn and Hg, throughout the tooth structures. We measured the elemental distribution inside the tooth from the root to the enamel, specially the region around the amalgam, after its total removal. Hg is present only in restored teeth and concentration profiles show strongly increased levels of this element close to the amalgam region, reaching 500 μg g -1 in one or two cases, decreasing strongly to the inner part of the tooth. Pb concentration profiles do not seem to be affected by metallic amalgam. Very high concentrations of Bi were found in one of the restored teeth, reaching more than 2000 μg g -1, decreasing sharply to the outer regions. The distribution of Mn, Fe, Cu and Zn was also determined in order to evaluate elemental influences by amalgam components. No significant changes in elemental concentrations were detected for Mn and Fe between healthy and restored teeth. However, the levels of Zn and Cu are increased in restored teeth. An X-ray fluorescence set-up with microprobe capabilities, 100 μm of spatial resolution and an energy of 18 keV, installed at LURE synchrotron (France) was used.

  17. Hg, Bi, Cu and Zn distribution in human teeth treated by dental amalgam measured by synchrotron microprobe

    Energy Technology Data Exchange (ETDEWEB)

    Carvalho, M.L. E-mail: luisa@cii.fc.ul.pt; Marques, J.P.; Brito, J.; Casaca, C.; Cunha, A.S

    2002-11-01

    Human teeth restored with dental amalgam were analysed by a synchrotron microprobe to evaluate the diffusion of its major constituents, Cu, Zn and Hg, throughout the tooth structures. We measured the elemental distribution inside the tooth from the root to the enamel, specially the region around the amalgam, after its total removal. Hg is present only in restored teeth and concentration profiles show strongly increased levels of this element close to the amalgam region, reaching 500 {mu}g g{sup -1} in one or two cases, decreasing strongly to the inner part of the tooth. Pb concentration profiles do not seem to be affected by metallic amalgam. Very high concentrations of Bi were found in one of the restored teeth, reaching more than 2000 {mu}g g{sup -1}, decreasing sharply to the outer regions. The distribution of Mn, Fe, Cu and Zn was also determined in order to evaluate elemental influences by amalgam components. No significant changes in elemental concentrations were detected for Mn and Fe between healthy and restored teeth. However, the levels of Zn and Cu are increased in restored teeth. An X-ray fluorescence set-up with microprobe capabilities, 100 {mu}m of spatial resolution and an energy of 18 keV, installed at LURE synchrotron (France) was used.

  18. HgCdTe e-APD detector arrays with single photon sensitivity for space lidar applications

    Science.gov (United States)

    Sun, Xiaoli; Abshire, James B.; Beck, Jeffrey D.

    2014-05-01

    A multi-element HgCdTe electron initiated avalanche photodiode (e-APD) array has been developed for space lidar. The detector array was fabricated with 4.3μm cutoff HgCdTe with a spectral response from 0.4 to 4.3 μm. We have demonstrated a 4x4 e-APD array with 80 μm square elements followed by a custom cryogenic CMOS read-out integrated circuit (ROIC). The device operates at 77K inside a small closed-cycle cooler-Dewar with the support electronics integrated in a field programmable gate array. Measurements showed a unity gain quantum efficiency of about 90% at 1.5-1.6 μm wavelength. The bulk dark current of the HgCdTe e-APD at 77K was less than 50,000 input referred electrons/s at 12 V APD bias where the APD gain was 620 and the measured noise equivalent power (NEP) was 0.4 fW/Hz1/2. The electrical bandwidth of the device was about 6 MHz, mostly limited by the ROIC, but sufficient for the lidar application. Although the devices were designed for low bandwidth pulse detections, the high gain and low dark current enabled them to be used for single photon detections. Because the APD was biased below the break-down voltage, the output is linear to the input signal and there were no nonlinear effect such as dead-time and afterpulsing, and no need for gated operation. A new series of HgCdTe e-APDs have also been developed with a much wider bandwidth ROIC and higher APD gain, which is expected to give a much better performance in single photon detections.

  19. 640 X 480 Pace HgCdTe FPA

    Science.gov (United States)

    Kozlowski, Lester J.; Bailey, Robert B.; Cabelli, Scott A.; Cooper, Donald E.; McComas, Gail D.; Vural, Kadri; Tennant, William E.

    1992-12-01

    A hybrid HgCdTe 640 X 480 infrared (IR) focal plane array (FPA) that meets the sensitivity, resolution, and field-of-view requirements of high-performance medium wavelength infrared (MWIR) imaging systems has been developed. The key technology making this large, high sensitivity device producible is the epitaxial growth of HgCdTe on a CdTe-buffered, sapphire substrate (referred to as PACE, for Producible Alternative to CdTe for Epitaxy; PACE-I refers to sapphire). The device offers TV resolution with excellent sensitivity at temperatures below 120 K. Mean NE(Delta) T as low as 13 mK has been achieved at operating temperatures nonuniformity compensation.

  20. Geochemical assessment of Hg pollution in gold mining sites

    Science.gov (United States)

    Rodrigues-Filho, S.; Villas Bôas, R. C.

    2003-05-01

    The increasing societal demand for actions and strategies towards sustainability of small-scale gold mining in developing countries has led experts to face the challenge of managing the harzards associated with mercury pollution from active and abandoned mine sites. Mercury pollution in drainage systems and its health effects are the most frequent subjects on environmental researchs dealing with small-scale gold mining worldwide. Also, filling of river beds with mineral matter originated from runoff of abandoned mining waste piles and tailings generally causes both silting of waterways and elevation of Hg concentrations in the environment. This paper summarizes the main results concerning the assessment of Hg pollution in Amazon drainage systems accomplished by the authors in the last decade in Brazil.

  1. Electrical Conductivity of HgTe at High Temperatures

    Science.gov (United States)

    Li, C.; Lehoczky, S. L.; Su, C.-H.; Scripa, R. N.

    2004-01-01

    The electrical conductivity of HgTe was measured using a rotating magnetic field method from 300 K to the melting point (943 K). A microscopic theory for electrical conduction was used to calculate the expected temperature dependence of the HgTe conductivity. A comparison between the measured and calculated conductivities was used to obtain the estimates of the temperature dependence of Gamma(sub 6)-Gamma(sub 8) energy gap from 300 K to 943 K. The estimated temperature coefficient for the energy gap was comparable to the previous results at lower temperatures (less than or equal to 300 K). A rapid increase in the conductivity just above 300 K and a subsequent decrease at 500 K is attributed to band crossover effects. This paper describes the experimental approach and some of the theoretical calculation details.

  2. Measurement of Linear Stark Interference in 199Hg

    CERN Document Server

    Loftus, T H; Griffith, W C; Romalis, M V; Heckel, B R; Fortson, E N

    2010-01-01

    We present measurements of Stark interference in the 6$^1S_0$ $\\rightarrow$ 6$^3P_1$ transition in $^{199}$Hg, a process whereby a static electric field $E$ mixes magnetic dipole and electric quadrupole couplings into an electric dipole transition, leading to $E$-linear energy shifts similar to those produced by a permanent atomic electric dipole moment (EDM). The measured interference amplitude, $a_{SI}$ = $(a_{M1} + a_{E2})$ = (5.8 $\\pm$ 1.5)$\\times 10^{-9}$ (kV/cm)$^{-1}$, agrees with relativistic, many-body predictions and confirms that earlier central-field estimates are a factor of 10 too large. More importantly, this study validates the capability of the $^{199}$Hg EDM search apparatus at the to resolve non-trivial, controlled, and sub-nHz Larmor frequency shifts with EDM-like characteristics.

  3. Measurement of linear stark interference in 199Hg.

    Science.gov (United States)

    Loftus, T H; Swallows, M D; Griffith, W C; Romalis, M V; Heckel, B R; Fortson, E N

    2011-06-24

    We present measurements of Stark interference in the (61)S(0)→6(3)P(1) transition in (199)Hg, a process whereby a static electric field E mixes magnetic dipole and electric quadrupole couplings into an electric dipole transition, leading to E-linear energy shifts similar to those produced by a permanent atomic electric dipole moment (EDM). The measured interference amplitude, a(SI) = (a(M1) + a(E2)) = (5.8 ± 1.5) × 10(-9) (kV / cm)(-1), agrees with relativistic, many-body predictions and confirms that earlier central-field estimates are a factor of 10 too large. More importantly, this study validates the capability of the (199)Hg EDM search apparatus to resolve nontrivial, controlled, and sub-nHz Larmor frequency shifts with EDM-like characteristics. PMID:21770639

  4. Measurement of Linear Stark Interference in Hg199

    Science.gov (United States)

    Loftus, T. H.; Swallows, M. D.; Griffith, W. C.; Romalis, M. V.; Heckel, B. R.; Fortson, E. N.

    2011-06-01

    We present measurements of Stark interference in the 6S01→6P13 transition in Hg199, a process whereby a static electric field E mixes magnetic dipole and electric quadrupole couplings into an electric dipole transition, leading to E-linear energy shifts similar to those produced by a permanent atomic electric dipole moment (EDM). The measured interference amplitude, aSI=(aM1+aE2)=(5.8±1.5)×10-9(kV/cm)-1, agrees with relativistic, many-body predictions and confirms that earlier central-field estimates are a factor of 10 too large. More importantly, this study validates the capability of the Hg199 EDM search apparatus to resolve nontrivial, controlled, and sub-nHz Larmor frequency shifts with EDM-like characteristics.

  5. Dynamic recycling of gaseous elemental mercury in the boundary layer of the Antarctic Plateau

    Directory of Open Access Journals (Sweden)

    A. Dommergue

    2012-07-01

    Full Text Available Gaseous elemental mercury (Hg(0 was investigated in the troposphere and in the interstitial air extracted from the snow at Dome Concordia station (alt. 3320 m on the Antarctic Plateau during January 2009. Measurements showed evidence of a very dynamic and daily cycling of Hg(0 inside the mixing layer with a range of values from 0.2 ng m−3 up to 2.3 ng m−3. During low solar irradiation periods, fast Hg(0 oxidation processes in a confined layer were observed leading to an enrichment of the upper snow layers in divalent Hg. Unexpectedly high Hg(0 concentrations for such a remote place were measured under higher solar irradiation due to the reemission of Hg(0 by the snowpack via photochemical reactions. Hg(0 concentrations showed a negative correlation with ozone mixing ratios, which contrasts with atmospheric mercury depletion events observed during the Arctic spring. It remains unclear whether halogens are involved in Hg(0 oxidation. We suggest that snow surfaces may play a role in promoting the heterogeneous oxidation of Hg(0. The cycling of other oxidants should be investigated together with Hg in order to clarify the complex reactivity on the Antarctic Plateau.

  6. Design and synthesis of BODIPY-clickate based Hg(2+) sensors: the effect of triazole binding mode with Hg(2+) on signal transduction.

    Science.gov (United States)

    Vedamalai, Mani; Kedaria, Dhaval; Vasita, Rajesh; Mori, Shigeki; Gupta, Iti

    2016-02-14

    BODIPY-clickates, F1 and F2, for the detection of Hg(2+) have been designed, synthesized and characterized. Both F1 and F2 showed hyperchromic shifts in the UV-visible spectra in response to increasing Hg(2+) concentrations. Hg(2+) ion binding caused perturbation of the emission quenching process and chelation induced enhanced bathochromic emission of F1 and F2 to 620 nm and 660 nm, respectively. Job's plot clearly indicated that the binding ratio of F1 and F2 with Hg(2+) was 1 : 1. The NMR titration of BODIPY-clickates with Hg(2+) confirmed that aromatic amines and triazoles were involved in the binding event. Furthermore, HRMS data of F1-Hg(2+) and F2-Hg(2+) supported the formation of mercury complexes of BODIPY-clickates. The dissociation constant for the interaction between fluorescent probes F1 and F2 with Hg(2+) was found to be 24.4 ± 5.1 μM and 22.0 ± 3.9 μM, respectively. The Hg(2+) ion induced fluorescence enhancement was almost stable in a pH range of 5 to 8. Having less toxicity to live cells, both the probes were successfully used to map the Hg(2+) ions in live A549 cells. PMID:26743311

  7. Numerical Simulation of the Modulation Transfer Function in HgCdTe Detector Arrays

    Science.gov (United States)

    Pinkie, Benjamin; Bellotti, Enrico

    2014-08-01

    In this work, we develop a method for simulating the modulation transfer function (MTF) of infrared detector arrays, which is based on numerical evaluation of the detector physics. The finite-difference time-domain and finite element methods are used to solve the electromagnetic and electrical equations for the device, respectively. We show how the total MTF can be deconvolved to examine the effects of specific physical processes. We introduce the MTF area difference and use it to quantify the effectiveness of several crosstalk mitigation techniques in improving the system MTF. We then apply our simulation methods to two-thirds generation mercury cadmium telluride (HgCdTe) detector architectures. The methodology is general, can be implemented with commercially available software, has experimentally realizable analogs, and is extendable to other material systems and device designs.

  8. The peculiar abundance pattern of the new Hg-Mn star HD 30085

    CERN Document Server

    Monier, R; Royer, F; Griffin, R E M

    2015-01-01

    Using high-dispersion, high-quality spectra of HD 30085 obtained with the echelle spectrograph SOPHIE at Observatoire de Haute Provence, we show that this star contains strong lines of the s-process elements Sr II, Y II and Zr II. Line syntheses of the lines yield large overabundances of Sr, Y, Zr which are characteristic of HgMn stars. The Sr-Y-Zr triad of abundances is inverted in HD 30085 compared to that in our solar system. The violation of the odd-even rule suggests that physical processes such as radiative diffusion, chemical fractionation and others must be at work in the atmosphere of HD 30085, and that the atmosphere is stable enough to sustain them.

  9. Inorganic arsenic - SPE HG-AAS method for RICE tested in-house and collaboratively

    DEFF Research Database (Denmark)

    Rasmussen, Rie Romme; Qian, Yiting; Sloth, Jens Jørgen

    Arsenic (As) is a trace element present in the environment and consequently in various food items, e.g. rice, which may contain relatively high concentration of arsenic compared to other foodstuffs of plant origin. Rice contains most often three forms of arsenic; inorganic arsenic (i...... and is one of the major contributors to the iAs exposure in many countries. The work presented here describes the development, validation and application of a simple and inexpensive method for inorganic arsenic (iAs) determination in rice samples. The separation of iAs from organoarsenic compounds (MA...... and DMA) was done by off-line solidphase extraction (SPE) followed by hydride generation atomic absorption spectrometry (HG-AAS) detection. Water bath heating (90 °C, 60 min) of samples with dilute nitric acid and hydrogen peroxide solubilised and oxidized all iAs to arsenate (AsV). Loading of buffered...

  10. Gammastrahlung vom Einfang thermischer Neutronen in Hg 199

    DEFF Research Database (Denmark)

    Maier, B.P.; Gruber, U.; Koch, H. R.;

    1965-01-01

    103 gamma transitions in Hg 200 have been observed. 37 of them were fitted into a level scheme which comprises 17 states. The energy of the one-phonon vibrational stateI=2+ has been determined to be 367.970±0.020 keV, that of the two-phonon vibrational triplet 947.34±0.07 keV, 1029.37±0.05 keV an...

  11. Hvordan understøttes hg-elevers kompetenceudvikling

    DEFF Research Database (Denmark)

    Svejgaard, Karin Løvenskjold; Hansen, Jens Ager; Karmark, Ole

    Publikationen handler om, hvordan hg-elever arbejder og dermed lærer og udvikler kvalifikationer og kompetencer i de undervisnings- og arbejdsformer, de indgår i. Indholdet er baseret på observationer af elever i klasseundervisning, gruppearbejde eller individuel arbejde i forlængelse af...... klasseundervisning og af elever i projektarbejde. Observationerne er gennemført på tre jyske handelsskoler....

  12. Maternal-fetal distribution of mercury ( sup 203 Hg) released from dental amalgam fillings

    Energy Technology Data Exchange (ETDEWEB)

    Vimy, M.J.; Takahashi, Y.; Lorscheider, F.L. (Univ. of Calgary, Alberta (Canada))

    1990-04-01

    In humans, the continuous release of Hg vapor from dental amalgam tooth restorations is markedly increased for prolonged periods after chewing. The present study establishes a time-course distribution for amalgam Hg in body tissues of adult and fetal sheep. Under general anesthesia, five pregnant ewes had twelve occlusal amalgam fillings containing radioactive 203Hg placed in teeth at 112 days gestation. Blood, amniotic fluid, feces, and urine specimens were collected at 1- to 3-day intervals for 16 days. From days 16-140 after amalgam placement (16-41 days for fetal lambs), tissue specimens were analyzed for radioactivity, and total Hg concentrations were calculated. Results demonstrate that Hg from dental amalgam will appear in maternal and fetal blood and amniotic fluid within 2 days after placement of amalgam tooth restorations. Excretion of some of this Hg will also commence within 2 days. All tissues examined displayed Hg accumulation. Highest concentrations of Hg from amalgam in the adult occurred in kidney and liver, whereas in the fetus the highest amalgam Hg concentrations appeared in liver and pituitary gland. The placenta progressively concentrated Hg as gestation advanced to term, and milk concentration of amalgam Hg postpartum provides a potential source of Hg exposure to the newborn. It is concluded that accumulation of amalgam Hg progresses in maternal and fetal tissues to a steady state with advancing gestation and is maintained. Dental amalgam usage as a tooth restorative material in pregnant women and children should be reconsidered.

  13. Maternal-fetal distribution of mercury (203Hg) released from dental amalgam fillings

    International Nuclear Information System (INIS)

    In humans, the continuous release of Hg vapor from dental amalgam tooth restorations is markedly increased for prolonged periods after chewing. The present study establishes a time-course distribution for amalgam Hg in body tissues of adult and fetal sheep. Under general anesthesia, five pregnant ewes had twelve occlusal amalgam fillings containing radioactive 203Hg placed in teeth at 112 days gestation. Blood, amniotic fluid, feces, and urine specimens were collected at 1- to 3-day intervals for 16 days. From days 16-140 after amalgam placement (16-41 days for fetal lambs), tissue specimens were analyzed for radioactivity, and total Hg concentrations were calculated. Results demonstrate that Hg from dental amalgam will appear in maternal and fetal blood and amniotic fluid within 2 days after placement of amalgam tooth restorations. Excretion of some of this Hg will also commence within 2 days. All tissues examined displayed Hg accumulation. Highest concentrations of Hg from amalgam in the adult occurred in kidney and liver, whereas in the fetus the highest amalgam Hg concentrations appeared in liver and pituitary gland. The placenta progressively concentrated Hg as gestation advanced to term, and milk concentration of amalgam Hg postpartum provides a potential source of Hg exposure to the newborn. It is concluded that accumulation of amalgam Hg progresses in maternal and fetal tissues to a steady state with advancing gestation and is maintained. Dental amalgam usage as a tooth restorative material in pregnant women and children should be reconsidered

  14. Selected elements in fly agaric Amanita muscaria.

    Science.gov (United States)

    Falandysz, J; Kunito, T; Kubota, R; Lipka, K; Mazur, A; Falandysz, Justyna J; Tanabe, S

    2007-09-01

    Concentrations of Ag, Al, Ba, Ca, Cd, Co, Cu, Cr, Cs, Fe, Ga, Hg, K, Mg, Mn, Mo, Na, Pb, Rb, Se, Sb, Sr, V, Tl and Zn have been determined in the whole fruiting bodies, as well as separately in caps and stalks, of fly agaric collected from three geographically distant sites in northern part of Poland. The elements were determined using ICP-MS, ICP-OES, HG-AAS and CV-AAS, respectively. For elements such as Al, Ba, Cr, Fe, Ga, Mo, Mn, Pb, Sb, Sr, Tl, and V concentrations were similar in the caps and stalks, respectively, and for K, Zn, Ag, Ca, Cd, Cu, Hg, Mg, Rb and Se were greater in the caps, while for Co, Cs and Na in the stalks. For Ag, Al, Ba, Ca, Cd, Co, Cr, Cs, Fe, Ga, Hg, Mn, Mo, Pb, Rb, Sb, Sr, Tl and V concentration in the caps showed spatial variations (P<0.05), while for Cu, K, Mg, Na, Se and Zn was independent of the site. The elements such as K with median or mean in the caps between 37,000 and 43,000 microg/g.dm and Mg with 920 and 1,100 microg/g dm were most abundant. Next, within median values range from approximately 100 to 500 microg/g dm were such as Ca, Fe and Al, and in descending order they followed by Rb (100-400 microg/g dm); V, Na, Zn (50-200 microg/g dm); Cu, Mn (10-50 microg/g dm); Cd (10-20 microg/g dm); Se (5 microg/g dm); Ba (<1-3); Cr, Ag, Pb, Sr (<1-2 microg/g dm); Cs, Co, Hg (<1-1 microg/g dm); Ga (<0.5), Sb, Mo and Tl (<0.1 microg/g dm). PMID:17849303

  15. Transuranium elements

    International Nuclear Information System (INIS)

    This paper reports that neutron irradiation of uranium, beginning in 1934, led to the reported discovery of such transuranium elements as eka-rhenium. After a few years of investigation these were correctly identified, in December 1938, as fission products. The first real transuranium elements, with atomic numbers 93 and 94 (neptumiun and plutionium), were discovered in 1940-1941. Plutomiun-239 was shown to be fission-able with slow neutrons, and chemical methods for its separation in quantity were developed. Not until it was recognized that transuranium elements should be part of a 14-member actinide series could elements 95 and 96 (americium and curium) be chemically identified after their nuclear synthesis. This new view was the key to the synthesis and identified after their nuclear synthesis. This new view was the key to the synthesis and identification of the next seven transuranium elements, resulting in the completion of the actinide series at element 103 in 1961. The transactinide elements could, according to the actinide concept, also be correctly placed in the periodic table, and the chemical properties of the first transactinide elements, elements 104 and 105 (rutherfordium and hafnium), confirm this point of view. Transuranium elements through number 109 are now known

  16. Factors influencing the large-scale distribution of Hg° in the Mexico City area and over the North Pacific

    Directory of Open Access Journals (Sweden)

    D. Blake

    2007-11-01

    Full Text Available Gas-phase elemental mercury (Hg° was measured aboard the NASA DC-8 aircraft during the Intercontinental Chemical Transport Experiment Phase B (INTEX-B campaign in spring 2006. Flights were conducted around Mexico City and on two subsequent deployments over the North Pacific based out of Honolulu, Hawaii and Anchorage, Alaska. Data obtained from 0.15–12 km altitude showed that Hg° exhibited a relatively constant vertical profile centered around 100 ppqv. Highly concentrated pollution plumes emanating from the Mexico City urban agglomeration revealed that mixing ratios of Hg° as large as 500 ppqv were related to combustion tracers such as CO, but not SO2 which is presumably released locally from coal burning, refineries, and volcanoes. Our analysis of Mexico City plumes indicated that widespread multi-source urban/industrial emissions may have a more important influence on Hg° than specific point sources. Over the Pacific, correlations with CO, CO2, CH4, and C2Cl4 were diffuse overall, but recognizable on flights out of Anchorage and Honolulu. In distinct plumes originating from the Asian continent the Hg°- CO relationship yielded an average value of ~0.56 ppqv/ppbv, in good agreement with previous findings. A prominent feature of the INTEX-B dataset was frequent total depletion of Hg° in the upper troposphere when stratospherically influenced air was encountered. Ozone data obtained with the differential absorption lidar (DIAL showed that the stratospheric impact on the tropospheric column was a common and pervasive feature on all flights out of Honolulu and Anchorage. We propose that this is likely a major factor driving large-scale seasonality in Hg° mixing ratios, especially at mid-latitudes, and an important process that should be incorporated into global chemical transport models.

  17. Factors influencing the large-scale distribution of Hg° in the Mexico City area and over the North Pacific

    Science.gov (United States)

    Talbot, R.; Mao, H.; Scheuer, E.; Dibb, J.; Avery, M.; Browell, E.; Sachse, G.; Vay, S.; Blake, D.; Huey, G.; Fuelberg, H.

    2008-04-01

    Gas-phase elemental mercury (Hg°) was measured aboard the NASA DC-8 aircraft during the Intercontinental Chemical Transport Experiment Phase B (INTEX-B) campaign in spring 2006. Flights were conducted around Mexico City and on two subsequent deployments over the North Pacific based out of Honolulu, Hawaii and Anchorage, Alaska. Data obtained from 0.15-12 km altitude showed that Hg° exhibited a relatively constant vertical profile centered around 100 ppqv. Highly concentrated pollution plumes emanating from the Mexico City urban agglomeration revealed that mixing ratios of Hg° as large as 500 ppqv were related to combustion tracers such as CO, but not SO2 which is presumably released locally from coal burning, refineries, and volcanoes. Our analysis of Mexico City plumes indicated that widespread multi-source urban/industrial emissions may have a more important influence on Hg° than specific point sources. Over the Pacific, correlations with CO, CO2, CH4, and C2Cl4 were diffuse overall, but recognizable on flights out of Anchorage and Honolulu. In distinct plumes originating from the Asian continent the Hg°- CO relationship yielded an average value of ~0.56 ppqv/ppbv, in good agreement with previous findings. A prominent feature of the INTEX-B dataset was frequent total depletion of Hg° in the upper troposphere when stratospherically influenced air was encountered. Ozone data obtained with the differential absorption lidar (DIAL) showed that the stratospheric impact on the tropospheric column was a common and pervasive feature on all flights out of Honolulu and Anchorage. We propose that this is likely a major factor driving large-scale seasonality in Hg° mixing ratios, especially at mid-latitudes, and an important process that should be incorporated into global chemical transport models.

  18. Factors influencing the large-scale distribution of Hg° in the Mexico City area and over the North Pacific

    Directory of Open Access Journals (Sweden)

    D. Blake

    2008-04-01

    Full Text Available Gas-phase elemental mercury (Hg° was measured aboard the NASA DC-8 aircraft during the Intercontinental Chemical Transport Experiment Phase B (INTEX-B campaign in spring 2006. Flights were conducted around Mexico City and on two subsequent deployments over the North Pacific based out of Honolulu, Hawaii and Anchorage, Alaska. Data obtained from 0.15–12 km altitude showed that Hg° exhibited a relatively constant vertical profile centered around 100 ppqv. Highly concentrated pollution plumes emanating from the Mexico City urban agglomeration revealed that mixing ratios of Hg° as large as 500 ppqv were related to combustion tracers such as CO, but not SO2 which is presumably released locally from coal burning, refineries, and volcanoes. Our analysis of Mexico City plumes indicated that widespread multi-source urban/industrial emissions may have a more important influence on Hg° than specific point sources. Over the Pacific, correlations with CO, CO2, CH4, and C2Cl4 were diffuse overall, but recognizable on flights out of Anchorage and Honolulu. In distinct plumes originating from the Asian continent the Hg°- CO relationship yielded an average value of ~0.56 ppqv/ppbv, in good agreement with previous findings. A prominent feature of the INTEX-B dataset was frequent total depletion of Hg° in the upper troposphere when stratospherically influenced air was encountered. Ozone data obtained with the differential absorption lidar (DIAL showed that the stratospheric impact on the tropospheric column was a common and pervasive feature on all flights out of Honolulu and Anchorage. We propose that this is likely a major factor driving large-scale seasonality in Hg° mixing ratios, especially at mid-latitudes, and an important process that should be incorporated into global chemical transport models.

  19. Electronic structure and optical properties of Cs2HgCl4: DFT calculations and X-ray photoelectron spectroscopy measurements

    Science.gov (United States)

    Lavrentyev, A. A.; Gabrelian, B. V.; Vu, V. T.; Parasyuk, O. V.; Fedorchuk, A. O.; Khyzhun, O. Y.

    2016-10-01

    A high-quality single crystal of cesium mercury tetrabromide, Cs2HgCl4, was synthesized by using the vertical Bridgman-Stockbarger method and its electronic structure was studied from both experimental and theoretical viewpoints. In particular, X-ray photoelectron spectra were measured for both pristine and Ar+ ion-bombarded Cs2HgCl4 single crystal surfaces. The present XPS measurements indicate that the Cs2HgCl4 single crystal surface is sensitive with respect to Ar+ ion-bombardment: such a treatment changes substantially its elemental stoichiometry. With the aim of exploring total and partial densities of states within the valence band and conduction band regions of the Cs2HgCl4 compound, band-structure calculations based on density functional theory (DFT) using the augmented plane wave + local orbitals (APW + lo) method as incorporated within the WIEN2k package are performed. The calculations indicate that the Cl 3p states are the principal contributors in the upper portion of the valence band, while the Hg 5d and Cs 5p states dominate in its lower portion. In addition, the calculations allow for concluding that the unoccupied Cl p and Hg s states are the main contributors to the bottom of the conduction band. Furthermore, main optical characteristics of Cs2HgCl4, namely dispersion of the absorption coefficient, real and imaginary parts of dielectric function, electron energy-loss spectrum, refractive index, extinction coefficient and optical reflectivity, are elucidated based on the DFT calculations.

  20. Stability and diffusion of Hg implanted YBa$_{2}$Cu$_{3}$O$_{6+x}$

    CERN Document Server

    Araújo, J P; Wahl, U; Marques, J G; Alves, E; Amaral, V S; Lourenço, A A; Galindo, V; Von Papen, T; Senateur, J P; Weiss, F; Vantomme, A; Langouche, G; Melo, A A; Da Silva, M F A; Soares, J C; Sousa, J B

    1999-01-01

    The radioactive isotope $^{197m}$Hg was implanted at 60 keV with low fluences (10$^{13}$ ions/cm$^{2}$ ) into YBa$_{2}$Cu$_{3}$O$_{6+x}$ (YBCO) superconducting thin films at ISOLDE/CERN. We report on the Hg dynamics and stability inside the YBCO lattice as a function of annealing temperature up to 890 K in vacuum or O$_{2}$ atmosphere. The perturbed angular correlation (PAC) technique was used for probing the Hg behavior at the atomic scale, while by monitoring the sample's activity in situ the Hg outdiffusion was studied. We found that Hg ions occupy unique lattice sites and that Hg should be bound to two apical oxygens. Hg diffusion occurs only for annealing temperatures above 653 K, in vacuum. The Hg migration energy was estimated to be EM = 1.58 $\\pm$ 0.15 eV.

  1. Fully relativistic coupled cluster and DFT study of electric field gradients at Hg in 199Hg compounds

    DEFF Research Database (Denmark)

    Arcisauskaité, Vaida; Knecht, Stefan; Sauer, Stephan P. A.;

    2012-01-01

    -relativistic (NR) calculations at the Hartree-Fock (HF), DFT, MP2 and coupled cluster (CC) levels. The relativistic and electron correlation contributions to EFG have opposite signs and are not additive, demonstrating the importance of taking into account relativistic and electron correlation contributions...... on an equal footing. DC-MP2 overestimates the electron correlation correction by 0.48-0.56 a.u. for Hg-halides and by 0.8 a.u. for Hg(CH3)2, respectively, while DC-CCSD underestimates the correlation correction by 0.57-0.66 a.u. compared to the reference DC-CCSD-T data. EFGs obtained at DC-DFT level vary...

  2. Crystal structure of the Hg{sub 4}SiS{sub 6} and Hg{sub 4}SiSe{sub 6} compounds

    Energy Technology Data Exchange (ETDEWEB)

    Gulay, L.D.; Olekseyuk, I.D.; Parasyuk, O.V

    2002-12-16

    The crystal structures of Hg{sub 4}SiS{sub 6} and Hg{sub 4}SiSe{sub 6} compounds were investigated using X-ray powder diffraction. These compounds crystallize in the monoclinic Cc space group with the lattice parameters a=1.23020(5), b=0.71031(4), c=1.22791(4) nm, {beta}=109.721(3) deg. for Hg{sub 4}SiS{sub 6} and a=1.28110(4), b=0.74034(4), c=1.27471(1) nm, {beta}=109.605(3) deg. for Hg{sub 4}SiSe{sub 6}. Atomic parameters were refined in the isotropic approximation (R{sub I}=0.0571 and R{sub I}=0.0555 for the Hg{sub 4}SiS{sub 6} and Hg{sub 4}SiSe{sub 6}, respectively)

  3. Investigation of 203,205Hg with the (d,pγ) reaction - identification of the i13/2 neutron hole state in 205Hg

    International Nuclear Information System (INIS)

    Low lying levels in 203Hg and 205Hg were studied with the (d, p) deuteron break-up reaction at Ed=14 and 18 MeV. Gamma-rays and conversion-electrons were measured in coincidence with protons. In addition delayed spectra were recorded with μs and ms beam pulsing. The i13/2 neutron hole state was identified in 205Hg and confirmed in 203Hg. The known level structure of 205Hg below 2 MeV is confirmed and extended. For 203Hg we observe the γ-decay of several levels below 1.5 MeV, which were previously known from transfer reactions. (orig.)

  4. Dielectric properties of nanophase Ag2HgI4 and Ag2HgI4–Al2O3 nanocomposites

    Indian Academy of Sciences (India)

    S Sankara Narayanan Potty; M Abdul Khadar

    2000-10-01

    The dielectric properties of nanophase Ag2HgI4 and Ag2HgI4–Al2O3 nanocomposites at different frequencies have been studied over a temperature range covering the stability range of phase of Ag2HgI4 and beyond the to phase transition temperature. ', tan and a.c. of nanophase Ag2HgI4 and Ag2HgI4–Al2O3 nanocomposites were found to be larger than the reported values for polycrystalline pellets of Ag2HgI4 . The dielectric properties of the nanocomposites were found to be a function of the wt.% of nano alumina. The observed changes are attributed to the grain boundary properties of nanophase materials and to the microsize space charge effects.

  5. Real-time selective visual monitoring of Hg2+ detection at ppt level: An approach to lighting electrospun nanofibers using gold nanoclusters

    Science.gov (United States)

    Senthamizhan, Anitha; Celebioglu, Asli; Uyar, Tamer

    2015-05-01

    In this work, fluorescent gold nanocluster (AuNC) decorated polycaprolactone (PCL) nanofibers (AuNC*PCL-NF) for real time visual monitoring of Hg2+ detection at ppt level in water is demonstrated. The resultant AuNC*PCL-NF exhibiting remarkable stability more than four months at ambient environment and facilitates increased accessibility to active sites resulting in improved sensing performance with rapid response time. The fluorescence changes of AuNC*PCL-NF and their corresponding time dependent spectra, upon introduction of Hg2+, led to the visual identification of the sensor performance. It is observed that the effective removal of excess ligand (bovine serum albumin (BSA) greatly enhances the surface exposure of AuNC and therefore their selective sensing performance is achieved over competent metal ions such as Cu2+, Ni2+, Mn2+, Zn2+, Cd2+, and Pb2+ present in the water. An exceptional interaction is observed between AuNC and Hg2+, wherein the absence of excess interrupting ligand makes AuNC more selective towards Hg2+. The underlying mechanism is found to be due to the formation of Au-Hg amalgam, which was further investigated with XPS, TEM and elemental mapping studies. In short, our findings may lead to develop very efficient fluorescent-based nanofibrous mercury sensor, keeping in view of its stability, simplicity, reproducibility, and low cost.

  6. 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.

  7. Interaction between mercury (Hg, arsenic (As and selenium (Se affects the activity of glutathione S-transferase in breast milk: possible relationship with fish and shellfish intake

    Directory of Open Access Journals (Sweden)

    Ramón Gaxiola-Robles

    2014-08-01

    Full Text Available Breast milk is regarded as an ideal source of nutrients for the growth and development of neonates, but it can also be a potential source of pollutants. Mothers can be exposed to different contaminants as a result of their lifestyle and environmental pollution. Mercury (Hg and arsenic (As could adversely affect the development of fetal and neonatal nervous system. Some fish and shellfish are rich in selenium (Se, an essential trace element that forms part of several enzymes related to the detoxification process, including glutathione S-transferase (GST. The goal of this study was to determine the interaction between Hg, As and Se and analyze its effect on the activity of GST in breast milk. Milk samples were collected from women between day 7 and 10 postpartum. The GST activity was determined spectrophotometrically; total Hg, As and Se concentrations were measured by atomic absorption spectrometry. To explain the possible association of Hg, As and Se concentrations with GST activity in breast milk, generalized linear models were constructed. The model explained 44% of the GST activity measured in breast milk. The GLM suggests that GST activity was positively correlated with Hg, As and Se concentrations. The activity of the enzyme was also explained by the frequency of consumption of marine fish and shellfish in the diet of the breastfeeding women.

  8. Impacts of forest harvesting on mobilization of Hg and MeHg in drained peatland forests on black schist or felsic bedrock.

    Science.gov (United States)

    Ukonmaanaho, Liisa; Starr, Mike; Kantola, Marjatta; Laurén, Ari; Piispanen, Juha; Pietilä, Heidi; Perämäki, Paavo; Merilä, Päivi; Fritze, Hannu; Tuomivirta, Tero; Heikkinen, Juha; Mäkinen, Jari; Nieminen, Tiina M

    2016-04-01

    Forest harvesting, especially when intensified harvesting method as whole-tree harvesting with stump lifting (WTHs) are used, may increase mercury (Hg) and methylmercury (MeHg) leaching to recipient water courses. The effect can be enhanced if the underlying bedrock and overburden soil contain Hg. The impact of stem-only harvesting (SOH) and WTHs on the concentrations of Hg and MeHg as well as several other variables in the ditch water was studied using a paired catchment approach in eight drained peatland-dominated catchments in Finland (2008-2012). Four of the catchments were on felsic bedrock and four on black schist bedrock containing heavy metals. Although both Hg and MeHg concentrations increased after harvesting in all treated sites according to the randomized intervention analyses (RIAs), there was only a weak indication of a harvest-induced mobilization of Hg and MeHg into the ditches. Furthermore, no clear differences between WTHs and SOH were found, although MeHg showed a nearly significant difference (p = 0.06) between the harvesting regimes. However, there was a clear bedrock effect, since the MeHg concentrations in the ditch water were higher at catchments on black schist than at those on felsic bedrock. The pH, suspended solid matter (SSM), dissolved organic carbon (DOC), and iron (Fe) concentrations increased after harvest while the sulfate (SO4-S) concentration decreased. The highest abundances of sulfate-reducing bacteria (SRB) were found on the sites with high MeHg concentrations. The biggest changes in ditch water concentrations occurred first 2 years after harvesting. PMID:26979172

  9. Analysis by neutron activation in moss samples for the determination of Cr, Se, As and Hg; Analisis por activacion neutronica en muestras de musgos para la determinacion de Cr, Se, As y Hg

    Energy Technology Data Exchange (ETDEWEB)

    Mejia C, R.; Garcia R, G. [Instituto Tecnologico de Toluca, Departamento de Posgrado, Av. Tecnologico s/n, Fraccionamiento La Virgen, 52149 Metepec, Estado de Mexico (Mexico); Lopez R, C.; Avila P, P.; Longoria G, L. C., E-mail: rosario.mejia@inin.gob.mx [ININ, Departamento del Reactor, Carretera Mexico-Toluca s/n, 52750 Ocoyoacac, Estado de Mexico (Mexico)

    2012-10-15

    This research work, presents a study of environmental monitoring in the Metropolitan Area of Toluca Valley using as bio-monitors to the mosses (bryophytes) native of different sites, analyzing the concentrations of As, Cr, Hg and Se, present in its structure. The analysis technique used to identify and to quantify to these elements was the Analysis by Neutron Activation, a nuclear analytic technique that allowed determining the concentrations at track level for its great versatility. Likewise the morphological study of the bryophyte Leskea angustata is presented by scanning electron microscopy. (Author)

  10. Phase transitions involving vacancy ordering in two metal mercuric iodides, Ag2HgI4 and Cu2HgI4

    Science.gov (United States)

    Lumsden, Mark; Steinitz, Michael; McAlduff, E. J.

    1995-06-01

    We have investigated the thermochromic order-disorder phase transitions in two superionic conducting compounds, Ag2HgI4 and Cu2HgI4, using capacitance dilatometry to determine the relative volume change, ΔV/V, at the transitions. We find an average ΔV/V of 9.6×10-3 for Ag2HgI4 at a transition temperature of 48.75 °C and an average ΔV/V of 4.0×10-3 for Cu2HgI4 at a transition temperature of 63 °C.

  11. Electric dipole moments of superheavy elements

    CERN Document Server

    Radžiūtė, Laima; Jönsson, Per; Bieroń, Jacek

    2015-01-01

    The multiconfiguration Dirac-Hartree-Fock (MCDHF) method was employed to calculate atomic electric dipole moments (EDM) of the superheavy element copernicium (Cn, $Z=112$). The EDM enhancement factors of Cn, here calculated for the first time, are about one order of magnitude larger than those of Hg. The exponential dependence of enhancement factors on atomic number $Z$ along group 12 of the periodic table was derived from the EDMs of the entire homolog series, $^{69}_{30}$Zn, $^{111}_{\\phantom{1}48}$Cd, $^{199}_{\\phantom{1}80}$Hg, $^{285}_{112}$Cn, and $^{482}_{162}$Uhb. These results show that superheavy elements with sufficiently large half-lives are good candidates for EDM searches.

  12. Manila clams from Hg polluted sediments of Marano and Grado lagoons (Italy) harbor detoxifying Hg resistant bacteria in soft tissues

    Energy Technology Data Exchange (ETDEWEB)

    Baldi, Franco, E-mail: baldi@unive.it [Dipartimento di Scienze Molecolari e Nanosistemi, Cà Foscari University of Venice, Dorsoduro 2137, 30123 Venice (Italy); Gallo, Michele; Marchetto, Davide [Dipartimento di Scienze Molecolari e Nanosistemi, Cà Foscari University of Venice, Dorsoduro 2137, 30123 Venice (Italy); Faleri, Claudia [Department of Environmental Science ‘G. Sarfatti’, University of Siena, 53100 Siena (Italy); Maida, Isabel; Fani, Renato [Dipartimento di Biologia Evoluzionistica, Via Romana, 17, University of Florence, 50125 Florence (Italy)

    2013-08-15

    A mechanism of mercury detoxification has been suggested by a previous study on Hg bioaccumulation in Manila clams (Ruditapes philippinarum) in the polluted Marano and Grado lagoons and in this study we demonstrate that this event could be partly related to the detoxifying activities of Hg-resistant bacteria (MRB) harbored in clam soft tissues. Therefore, natural clams were collected in six stations during two different periods (winter and spring) from Marano and Grado Lagoons. Siphons, gills and hepatopancreas from acclimatized clams were sterile dissected to isolate MRB. These anatomical parts were glass homogenized or used for whole, and they were lying on a solid medium containing 5 mg l{sup −1} HgCl{sub 2} and incubated at 30 °C. A total of fourteen bacterial strains were isolated and were identified by 16S rDNA sequencing and analysis, revealing that strains were representative of eight bacterial genera, four of which were Gram-positive (Enterococcus, Bacillus, Jeotgalicoccus and Staphylococcus) and other four were Gram-negative (Stenotrophomonas, Vibrio, Raoultella and Enterobacter). Plasmids and merA genes were found and their sequences determined. Fluorescence in situ hybridization (FISH) technique shows the presence of Firmicutes, Actinobacteria and Gammaproteobacteria by using different molecular probes in siphon and gills. Bacterial clumps inside clam flesh were observed and even a Gram-negative endosymbiont was disclosed by transmission electronic microscope inside clam cells. Bacteria harbored in cavities of soft tissue have mercury detoxifying activity. This feature was confirmed by the determination of mercuric reductase in glass-homogenized siphons and gills. -- Highlights: ► We isolated Gram-positive and Gram-negative Hg resistant strains from soft tissues of Ruditapes philippinarum. ► We identify 14 mercury resistant strains by 16S rRNA gene sequences. ► Bacteria in siphon and gill tissues of clams were observed by TEM and identified

  13. Probabilistic meta-analysis of risk from the exposure to Hg in artisanal gold mining communities in Colombia.

    Science.gov (United States)

    De Miguel, Eduardo; Clavijo, Diana; Ortega, Marcelo F; Gómez, Amaia

    2014-08-01

    Colombia is one of the largest per capita mercury polluters in the world as a consequence of its artisanal gold mining activities. The severity of this problem in terms of potential health effects was evaluated by means of a probabilistic risk assessment carried out in the twelve departments (or provinces) in Colombia with the largest gold production. The two exposure pathways included in the risk assessment were inhalation of elemental Hg vapors and ingestion of fish contaminated with methyl mercury. Exposure parameters for the adult population (especially rates of fish consumption) were obtained from nation-wide surveys and concentrations of Hg in air and of methyl-mercury in fish were gathered from previous scientific studies. Fish consumption varied between departments and ranged from 0 to 0.3 kg d(-1). Average concentrations of total mercury in fish (70 data) ranged from 0.026 to 3.3 μg g(-1). A total of 550 individual measurements of Hg in workshop air (ranging from gold mining communities in Colombia. PMID:24534152

  14. Probabilistic meta-analysis of risk from the exposure to Hg in artisanal gold mining communities in Colombia.

    Science.gov (United States)

    De Miguel, Eduardo; Clavijo, Diana; Ortega, Marcelo F; Gómez, Amaia

    2014-08-01

    Colombia is one of the largest per capita mercury polluters in the world as a consequence of its artisanal gold mining activities. The severity of this problem in terms of potential health effects was evaluated by means of a probabilistic risk assessment carried out in the twelve departments (or provinces) in Colombia with the largest gold production. The two exposure pathways included in the risk assessment were inhalation of elemental Hg vapors and ingestion of fish contaminated with methyl mercury. Exposure parameters for the adult population (especially rates of fish consumption) were obtained from nation-wide surveys and concentrations of Hg in air and of methyl-mercury in fish were gathered from previous scientific studies. Fish consumption varied between departments and ranged from 0 to 0.3 kg d(-1). Average concentrations of total mercury in fish (70 data) ranged from 0.026 to 3.3 μg g(-1). A total of 550 individual measurements of Hg in workshop air (ranging from Colombia.

  15. Magneto-optical transitions between subbands with different quantum numbers in narrow gap HgTe-CdTe superlattices

    Science.gov (United States)

    Luo, H.; Yang, G. L.; Furdyna, J. K.; Ram-Mohan, L. R.

    1991-10-01

    Magneto-optical transitions induced by the coupling between the conduction and the valence bands through the momentum matrix element, and by the coupling terms between light and heavy holes resulting from an applied magnetic field are studied theoretically in narrow gap HgTe-CdTe superlattices. Selection rules and transition probabilities for the above transitions are presented and compared with allowed transitions. The numerical results for the transition probabilities show that some of the interband transitions with ΔN=±1 are significant and have to be considered in the studies of interband magneto-optical spectra of narrow gap superlattices.

  16. Reduced trace element concentrations in fast-growing juvenile Atlantic salmon in natural streams

    OpenAIRE

    Ward, Darren M.; Keith H Nislow; Celia Y. Chen; Folt, Carol L

    2010-01-01

    To assess the effect of rapid individual growth on trace element concentrations in fish, we measured concentrations of seven trace elements (As, Cd, Cs, Hg, Pb, Se, Zn) in stream-dwelling Atlantic salmon (Salmo salar) from 15 sites encompassing a 10-fold range in salmon growth. All salmon were hatched under uniform conditions, released into streams, and sampled ~120 days later for trace element analysis. For most elements, element concentrations in salmon tracked those in their prey. Fast-gro...

  17. Luminescence studies of HgCdTe alloys

    OpenAIRE

    Hunter, A. T.; McGill, T. C.

    1982-01-01

    We report the observation in Hg_(1-x)Cd_(x)Te of band-to-band, band-to-acceptor, and donor-acceptor luminescence for material of x = 0.32 and 0.5, and bound exciton recombination luminescence, for material of x = 0.5. The band-to-band lineshape and variation in intensity with pump power are appropriate to an electron-hole plasma with recombination proceeding without wave vector conservation. Differences between the spectra among the four 0. 5 samples studied are attributed to variations in...

  18. Measurement of Linear Stark Interference in 199Hg

    OpenAIRE

    Loftus, T. H.; Swallows, M. D.; Griffith, W. C.; Romalis, M. V.; Heckel, B. R.; Fortson, E. N.

    2010-01-01

    We present measurements of Stark interference in the 6$^1S_0$ $\\rightarrow$ 6$^3P_1$ transition in $^{199}$Hg, a process whereby a static electric field $E$ mixes magnetic dipole and electric quadrupole couplings into an electric dipole transition, leading to $E$-linear energy shifts similar to those produced by a permanent atomic electric dipole moment (EDM). The measured interference amplitude, $a_{SI}$ = $(a_{M1} + a_{E2})$ = (5.8 $\\pm$ 1.5)$\\times 10^{-9}$ (kV/cm)$^{-1}$, agrees with rela...

  19. Trace-Element Constraints on Origin of SiO2-bearing Clasts in Ordinary Chondrites

    Science.gov (United States)

    Misawa, K.; Kanazawa, M.; Bridges, J. C.; Nakamura, N.; Hutchison, R.

    1995-09-01

    Silica-rich igneous-textured clasts are found in OC [1-6]. The SiO2-bearing clasts found in the Parnallee (LL3.6) and Farmington (L5) chondrites are isotopically unique [4-6]. They plot on a mixing line defined between UOC chondrules and an 16(sub)O-depleted end member in the oxygen three isotope diagram. We analyzed trace elements including REE by MSID technique for SiO2-bearing clasts (CB1, CB4, CB7, and CB8) from Parnallee. Some major and minor elements of CB8 were determined by AA or ICP-AES. The CI-chondrite normalized REE patterns of the clasts are shown in Fig. 1. CB8 has a high Si/Mg ratio (2.5), although its bulk Mg/(Mg + Fe) and Fe/Mn ratios (0.79 and 51, respectively) are within the range of chondritic values. Refractory elements Ca and Al are highly fractionated in CB8; the clast is enriched in Ca (3 x CI) but depleted in Al (0.7 x CI). CB1, CB4, and CB7 also show Ca enrichment (3-7 x CI). CB8 is depleted in moderately volatile lithophiles Mn, Na, K, and Rb (0.18-0.71 x CI), siderophile elements Fe, Co, and Ni (0.0041-0.39 x CI), and chalcophile element Zn (0.076 x CI). The SiO2-bearing clasts analyzed exhibit a gradual depletion from LREE to HREE (CI-normalized La/Lu ratios vary from 1.6 to 18) and a large positive Eu anomaly (Eu/Eu*=2.4-14) along with a depletion of La. This LREE/HREE fractionation is inversely correlated with SiO2 contents of the clasts. Abundance of Sr is parallel to that of Eu in CB8. However, Sr is depleted compared with Eu in the other clasts. These abundance patterns are quite different from those of typical ferromagnesian chondrules in UOCs, SiO2-bearing pyroxene-rich clast in Hedjaz (L3.7) [3], and silica-rich orthopyroxenite Bo-1 in Bovedy (L3) [7]. Absence of metal and sulfide, low abundances of siderophile and chalcophile elements in the clasts imply that metal and sulfide were removed from precursor material before or during clast formation. General REE patterns of SiO2-bearing clasts from Parnallee suggest that they were

  20. 203Hg binding in the liver and kidney of the frog, Rana tigrina

    International Nuclear Information System (INIS)

    Following a single i.p. dose of the radioisotope, 203Hg was found to accumulate in both the high and low molecular weight (MW) fractions of the kidney and liver of the frog. The course of 203Hg appearance in the 2 fractions varied in the liver; 203Hg was exclusively associated with the higher MW fractions at 2 days whereas the radiotracer appeared in both low and high MW fractions at 4 and 7 days after administration. In the kidneys, however, 203Hg was associated with high and low MW fractions at all the intervals studied. Low MW 203Hg binding fraction appeared to be a metallothionein-like substance. (Auth.)

  1. A density functional theory study of the adsorption of Hg and HgCl2 on a CaO(001) surface

    Institute of Scientific and Technical Information of China (English)

    GUO Xin; ZHENG Chuguang; LU Nanxia

    2007-01-01

    The adsorption of mercury and mercury chloride on a CaO(001) surface was investigated by the density functional theory (DFT) by using Ca9O9 cluster embedded in an electrostatic field represented by 178 point charges at the crystal CaO lattice positions.For the mercury molecular axis normal to the surface,the mercury can only coordinate to the O2- anion and has a very weak binding energy of 19.649 kJ/mol.When the mercury chloride molecular axis is vertical to the surface,the Cl atom coordinates to the Ca2+ cation and has a binding energy of 23.699 kJ/mol.When the mercury chloride molecular axis is parallel to the surface,the Hg atom coordinates to the O2- anion and has a binding energy of 87.829 kJ/mol,which means that the parallel geometry is more stable than the vertical one.The present calculations show that CaO injection could substantially reduce gaseous mercury chloride,but have no apparent effect on the mercury,which is compatible with the available experimental results.This research will provide valuable information for optimizing and selecting a sorbent for the trace element in flue gas.

  2. Trend and characteristics of atmospheric emissions of Hg, As, and Se from coal combustion in China, 1980-2007

    Science.gov (United States)

    Tian, H. Z.; Wang, Y.; Xue, Z. G.; Cheng, K.; Qu, Y. P.; Chai, F. H.; Hao, J. M.

    2010-12-01

    Emissions of hazardous trace elements in China are of great concern because of their negative impacts on local air quality as well as on regional environmental health and ecosystem risks. In this paper, the atmospheric emissions of mercury (Hg), arsenic (As), and selenium (Se) from coal combustion in China for the period 1980-2007 are estimated on the basis of coal consumption data and emission factors, which are specified by different categories of combustion facilities, coal types, and the equipped air pollution control devices configuration (Dust collectors, FGD, etc.). Specifically, multi-year emission inventories of Hg, As, and Se from 30 provinces and 4 economic sectors (thermal power, industry, residential use, and others) are evaluated and analyzed in detail. Furthermore, the gridded distribution of provincial-based Hg, As, and Se emissions in 2005 at a resolution of 1° × 1° is also plotted. It shows that the calculated national total atmospheric emissions of Hg, As, and Se from coal combustion have rapidly increased from 73.59 t, 635.57 t, and 639.69 t in 1980 to 305.95 t, 2205.50 t, and 2352.97 t in 2007, at an annually averaged growth rate of 5.4%, 4.7%, and 4.9%, respectively. The industrial sector is the largest source for Hg, As, and Se, accounting for about 50.8%, 61.2%, and 56.2% of the national totals, respectively. The share of power plants is 43.3% for mercury, 24.9% for arsenic, and 33.4% for selenium, respectively. Also, it shows remarkably different regional contribution characteristics of these 3 types of trace elements, the top 5 provinces with the heaviest mercury emissions in 2007 are Shandong (34.40 t), Henan (33.63 t), Shanxi (21.14 t), Guizhou (19.48 t), and Hebei (19.35 t); the top 5 provinces with the heaviest arsenic emissions in 2007 are Shandong (219.24 t), Hunan (213.20 t), Jilin (141.21 t), Hebei (138.54 t), and Inner Mongolia (127.49 t); while the top 5 provinces with the heaviest selenium emissions in 2007 are Shandong (289

  3. Trend and characteristics of atmospheric emissions of Hg, As, and Se from coal combustion in China, 1980–2007

    Directory of Open Access Journals (Sweden)

    H. Z. Tian

    2010-09-01

    Full Text Available Emissions of hazardous trace elements in China are of great concern because of their negative impacts on local air quality as well as on regional environmental health and ecosystem risks. In this paper, the atmospheric emissions of mercury (Hg, arsenic (As, and selenium (Se from coal combustion in China for the period 1980–2007 are estimated on the basis of coal consumption data and emission factors, which are specified by different categories of combustion facilities, coal types, and the equipped air pollution control devices configuration (Dust collectors, FGD, etc.. Specifically, multi-year emission inventories of Hg, As, and Se from 30 provinces and 4 economic sectors (thermal power, industry, residential use, and others are evaluated and analyzed in detail. Furthermore, the gridded distribution of provincial-based Hg, As, and Se emissions in 2005 at a resolution of 1°×1° is also plotted. It shows that the calculated national total atmospheric emissions of Hg, As, and Se from coal combustion have rapidly increased from 73.59 t, 635.57 t, and 639.69 t in 1980 to 305.95 t, 2205.50 t, and 2352.97 t in 2007, at an annually averaged growth rate of 5.4%, 4.7%, and 4.9%, respectively. The industrial sector is the largest source for Hg, As, and Se, accounting for about 50.8%, 61.2%, and 56.2% of the national totals, respectively. The share of power plants is 43.3% for mercury, 24.9% for arsenic, and 33.4% for selenium, respectively. Also, it shows remarkably different regional contribution characteristics of these 3 types of trace elements, the top 5 provinces with the heaviest mercury emissions in 2007 are Shandong (34.40 t, Henan (33.63 t, Shanxi (21.14 t, Guizhou (19.48 t, and Hebei (19.35 t; the top 5 provinces with the heaviest arsenic emissions in 2007 are Shandong (219.24 t, Hunan (213.20 t, Jilin (141.21 t, Hebei (138.54 t, and Inner Mongolia (127.49 t; while the top 5 provinces with the heaviest selenium emissions in 2007 are Shandong

  4. Pulsed corona discharge for oxidation of gaseous elemental mercury - article no. 251503

    Energy Technology Data Exchange (ETDEWEB)

    Ko, K.B.; Byun, Y.; Cho, M.; Namkung, W.; Hamilton, I.P.; Shin, D.N.; Koh, D.J.; Kim, K.T. [Research Institute for Industrial Science & Technology, Pohang (Republic of Korea)

    2008-06-15

    Positive pulsed corona discharge has been applied for the oxidation of gaseous elemental mercury (Hg{sup O} from a simulated flue gas. The oxidation of Hg{sup 0} to Hg{sup O} and HgCl{sub 2} can significantly enhance the mercury removal from flue gas. At a gas condition of O{sub 2} (10%), H{sub 2}O (3%), and N{sub 2} (balance), Hg{sup 0} oxidation efficiency of 84% was achieved at an input energy density of 45 J/l. The presence of NO, however, hinders Hg{sup 0} oxidation due to the preferential reaction of NO with O and O{sub 3}. On the contrary, SO{sub 2} shows little effect on Hg{sup 0} oxidation due to its preferential reaction with OH. It has been also observed that the HCl in gas stream can be dissociated to Cl and Cl{sub 2} and can induce additional Hg{sup 0} oxidation to HgCl{sub 2}.

  5. Quantifying the effects of soil temperature, moisture and sterilization on elemental mercury formation in boreal soils.

    Science.gov (United States)

    Pannu, Ravinder; Siciliano, Steven D; O'Driscoll, Nelson J

    2014-10-01

    Soils are a source of elemental mercury (Hg(0)) to the atmosphere, however the effects of soil temperature and moisture on Hg(0) formation is not well defined. This research quantifies the effect of varying soil temperature (278-303 K), moisture (15-80% water filled pore space (WFPS)) and sterilization on the kinetics of Hg(0) formation in forested soils of Nova Scotia, Canada. Both, the logarithm of cumulative mass of Hg(0) formed in soils and the reduction rate constants (k values) increased with temperature and moisture respectively. Sterilizing soils significantly (p < 0.05, n = 10) decreased the percent of total Hg reduced to Hg(0). We describe the fundamentals of Hg(0) formation in soils and our results highlight two key processes: (i) a fast abiotic process that peaks at 45% WFPS and depletes a small pool of Hg(0) and; (ii) a slower, rate limiting biotic process that generates a large pool of reducible Hg(II). PMID:25016467

  6. Injury of Hg2+ and DBS on Lemna minor%Hg2+、DBS对浮萍的伤害研究

    Institute of Scientific and Technical Information of China (English)

    马剑敏; 王琳; 杜晋立; 吴晶敏

    2001-01-01

    The injury degree of Lemna minor by the stress of Hg2+ and DBSare reported.The concentrations of chlorophyll and dissolved protein decrease with the increase of Hg2+ and DBS concentrations or as treatment time is continued,dead percentage increase with the increase of Hg2+ and DBS concentrations or as treatment time is continued.When the concentrations of HgCl2 is 6mg/L or DBS is 12mg/L,about 70% of Lemna minor can live for 10 days at least.%研究了在Hg2+、DBS胁迫下,浮萍(LemnaminorL.)植株的枯死率、叶绿素含量和可溶性蛋白质含量的变化。植株的枯死率随Hg2+、DBS浓度升高和处理时间的延长而增加;叶绿素和蛋白质含量随Hg2+和DBS浓度升高和处理时间的延长而逐渐下降。在HgCl2、DBS浓度分别为6mg/L、12mg/L时,约70%的浮萍10d内仍存活。

  7. Investigation of the use of an {alpha} + Xn reaction channel to enhance the population of superdeformed states in {sup 193}Hg and {sup 195}Hg

    Energy Technology Data Exchange (ETDEWEB)

    Zwartz, G.; Drake, T.E.; Cromaz, M. [Department of Physics, University of Toronto, Toronto, Ontario M5S-1A7 (Canada); Ward, D.; Janzen, V.; Galindo-Uribarri, A. [Chalk River Laboratories, Chalk River, Ontario K0J-1J0 (Canada); Prevost, D.; Waddington, J.; Mullins, S.M. [Department of Physics and Astronomy, McMaster University, Hamilton, Ontario L8S-4K1 (Canada)

    2000-11-01

    A study was made to determine whether the population of superdeformed states in {sup 193}Hg and {sup 195}Hg can be enhanced by using reactions in which alpha particles are emitted. The search utilized a {sup 184}W({sup 18}O,{alpha} Xn) reaction at 115 and 120 MeV for the {sup 193}Hg study and a {sup 186}W({sup 18}O,{alpha} Xn) reaction at 105 and 110 MeV for the {sup 195}Hg study. Two known superdeformed states of {sup 193}Hg were observed. The intensities of the superdeformed states in {sup 193}Hg populated by a reaction involving the emission of an alpha particle were found to be reduced by at least a factor of four relative to the intensities of these states produced in reactions involving only the emission of neutrons and {gamma}-rays. No rotational bands built on superdeformed states in {sup 195}Hg with transition intensities >0.8% of the total {sup 195}Hg yield were found. Evidence is shown that the energy of the alpha particle that is associated with superdeformed states may be lower than that of alpha particles associated with normally deformed states. (author)

  8. Uptake of Hg2+ by picocyanobacteria in natural water from four Andean lakes

    Directory of Open Access Journals (Sweden)

    Diéguez M.C.

    2014-07-01

    Full Text Available In lake food webs, planktonic bacteria and algae represent the greatest bioconcentration step for Hg2+ and monomethyl-Hg (MeHg. As they are the most abundant organisms in planktonic trophic webs and also the main food resource for herbivorous plankton, they can mobilize large amounts of Hg to higher trophic levels. In Andean Patagonian lakes (Argentina, dissolved organic matter (DOM concentration and character, coupled with photo-reactions, play a central role in the complexation of Hg2+ in the water column and can even regulate the uptake of Hg2+ by planktonic algae. In this investigation we evaluated the DOM character of natural waters (NW from four Andean lakes and studied its influence on the uptake of 197Hg2+ in a strain of the picocyanobacteria Synechococcus by using Hg2+ labeled with 197Hg2+. The uptake of radiolabeled Hg2+ by Synechococcus showed different magnitude in NW of lakes Moreno, El Trébol, Morenito and Escondido. Increasing lake DOM concentration reduced the bioavailability of Hg2+ as indicated by the lower uptakes rates found in NW with higher complexity and concentration of the DOM pool. Uptakes of Hg2+ by this picocyanobacteria contrasted among NW from pelagic (surface and bottom and littoral compartments of Lake Escondido which suggest that the entry of this metal may be highly variable even in the same environment. The study of the uptake of radiolabeled Hg2+ in a set of dilutions of NW from Lake Escondido demonstrated that the bioavailability of Hg2+ decrease with increasing DOM concentration.

  9. Concentrations of 17 elements, including mercury, in the tissues, food and abiotic environment of Arctic shorebirds

    International Nuclear Information System (INIS)

    Exposure to contaminants is one hypothesis proposed to explain the global decline in shorebirds, and is also an increasing concern in the Arctic. We assessed potential contaminants (As, Be, Cd, Co, Cr, Cu, Fe, Hg, Mn, Mo, Ni, Pb, Sb, Se, Tl, V, and Zn) at a shorebird breeding site in Nunavut, Canada. We compared element levels in soil, invertebrates and shorebird blood to assess evidence for bioconcentration and biomagnification within the Arctic-based food chain. We tested whether elements in blood, feathers and eggs of six shorebird species (Pluvialis squatarola, Calidris alpina, C. fuscicollis, Phalaropus fulicarius, Charadrius semipalmatus, and Arenaria interpres) were related to fitness endpoints: adult body condition, blood-parasite load, egg size, eggshell thickness, nest duration, and hatching success. To facilitate comparison to other sites, we summarise the published data on toxic metals in shorebird blood and egg contents. Element concentrations and invertebrate composition differed strongly among habitats, and habitat use and element concentrations differed among shorebird species. Hg, Se, Cd, Cu, and Zn bioconcentrated from soil to invertebrates, and Hg, Se and Fe biomagnified from invertebrates to shorebird blood. As, Ni, Pb, Co and Mn showed significant biodilution from soil to invertebrates to shorebirds. Soil element levels were within Canadian guidelines, and invertebrate Hg levels were below dietary levels suggested for the protection of wildlife. However, maximum Hg in blood and eggs approached levels associated with toxicological effects and Hg-pollution in other bird species. Parental blood-Hg was negatively related to egg volume, although the relationship varied among species. No other elements approached established toxicological thresholds. In conclusion, whereas we found little evidence that exposure to elements at this site is leading to the declines of the species studied, Hg, as found elsewhere in the Canadian Arctic, is of potential

  10. Concentrations of 17 elements, including mercury, in the tissues, food and abiotic environment of Arctic shorebirds

    Energy Technology Data Exchange (ETDEWEB)

    Hargreaves, Anna L., E-mail: alhargreaves@gmail.com [Calgary Zoo, Centre for Conservation Research, 1300 Zoo Rd NE, Calgary, AB, T2E 7V6 (Canada); Whiteside, Douglas P. [Calgary Zoo, Animal Health Centre, 1300 Zoo Rd NE, Calgary, AB, T2E 7V6 (Canada); University of Calgary, Department of Ecosystem and Public Health, Faculty of Veterinary Medicine, 2500 University Dr. NW, Calgary, AB, T2N 1N4 (Canada); Gilchrist, Grant [Carleton University, National Wildlife Research Centre, Ottawa, ON, KIA OH3 (Canada)

    2011-09-01

    Exposure to contaminants is one hypothesis proposed to explain the global decline in shorebirds, and is also an increasing concern in the Arctic. We assessed potential contaminants (As, Be, Cd, Co, Cr, Cu, Fe, Hg, Mn, Mo, Ni, Pb, Sb, Se, Tl, V, and Zn) at a shorebird breeding site in Nunavut, Canada. We compared element levels in soil, invertebrates and shorebird blood to assess evidence for bioconcentration and biomagnification within the Arctic-based food chain. We tested whether elements in blood, feathers and eggs of six shorebird species (Pluvialis squatarola, Calidris alpina, C. fuscicollis, Phalaropus fulicarius, Charadrius semipalmatus, and Arenaria interpres) were related to fitness endpoints: adult body condition, blood-parasite load, egg size, eggshell thickness, nest duration, and hatching success. To facilitate comparison to other sites, we summarise the published data on toxic metals in shorebird blood and egg contents. Element concentrations and invertebrate composition differed strongly among habitats, and habitat use and element concentrations differed among shorebird species. Hg, Se, Cd, Cu, and Zn bioconcentrated from soil to invertebrates, and Hg, Se and Fe biomagnified from invertebrates to shorebird blood. As, Ni, Pb, Co and Mn showed significant biodilution from soil to invertebrates to shorebirds. Soil element levels were within Canadian guidelines, and invertebrate Hg levels were below dietary levels suggested for the protection of wildlife. However, maximum Hg in blood and eggs approached levels associated with toxicological effects and Hg-pollution in other bird species. Parental blood-Hg was negatively related to egg volume, although the relationship varied among species. No other elements approached established toxicological thresholds. In conclusion, whereas we found little evidence that exposure to elements at this site is leading to the declines of the species studied, Hg, as found elsewhere in the Canadian Arctic, is of potential

  11. Mercury methylation in paddy soil: source and distribution of mercury species at a Hg mining area, Guizhou Province, China

    Science.gov (United States)

    Zhao, Lei; Anderson, Christopher W. N.; Qiu, Guangle; Meng, Bo; Wang, Dingyong; Feng, Xinbin

    2016-04-01

    Rice paddy plantation is the dominant agricultural land use throughout Asia. Rice paddy fields have been identified as important sites for methylmercury (MeHg) production in the terrestrial ecosystem and a primary pathway of MeHg exposure to humans in mercury (Hg) mining areas. We compared the source and distribution of Hg species in different compartments of the rice paddy during a complete rice-growing season at two different typical Hg-contaminated mining sites in Guizhou province, China: an abandoned site with a high Hg concentration in soil but a low concentration in the atmosphere and a current-day artisanal site with a low concentration in soil but a high concentration in the atmosphere. Our results showed that the flux of new Hg to the ecosystem from irrigation and atmospheric deposition was insignificant relative to the pool of old Hg in soil; the dominant source of MeHg to paddy soil is in situ methylation of inorganic Hg (IHg). Elevated MeHg concentrations and the high proportion of Hg as MeHg in paddy water and the surface soil layer at the artisanal site demonstrated active Hg methylation at this site only. We propose that the in situ production of MeHg in paddy water and surface soil is dependent on elevated Hg in the atmosphere and the consequential deposition of new Hg into a low-pH anoxic geochemical system. The absence of depth-dependent variability in the MeHg concentration in soil cores collected from the abandoned Hg mining site, consistent with the low concentration of Hg in the atmosphere and high pH of the paddy water and irrigation water, suggested that net production of MeHg at this site was limited. We propose that the concentration of Hg in ambient air is an indicator for the risk of MeHg accumulation in paddy rice.

  12. A State-of-the-Science Hg Redox Mechanism for Atmospheric Models: Constraints from Observations and Global Implications

    Science.gov (United States)

    Horowitz, H.; Jacob, D. J.; Amos, H. M.; Streets, D. G.; Zhang, Y.; Dibble, T. S.; Slemr, F.; Sunderland, E. M.

    2015-12-01

    Mercury (Hg) in the atmosphere cycles between two redox forms, Hg0 and HgII. Hg0 has a lifetime of ~1 year allowing near-global transport, while HgII is efficiently removed by deposition within weeks. Understanding atmospheric Hg redox chemistry is critical to determining the patterns of deposition to the surface, where Hg can be transformed to the bioaccumulative neurotoxin, methylmercury. We present a state-of-the-science redox mechanism for use in atmospheric models, with new theoretical data, which we implement in a global 3-D chemical transport model (GEOS-Chem). We evaluate our simulation against atmospheric observations and examine implications for Hg deposition. Modeled HgII wet deposition depends on the oxidation of anthropogenic, ocean, and soil Hg0 emissions and the reduction of emitted anthropogenic HgII. We present a new global anthropogenic atmospheric Hg emissions inventory for 1990 - 2010 with improved speciation of power plant emissions and regional commercial Hg emissions. The seasonal cycle of ocean evasion is also critical to atmospheric Hg variability. We present an advance in our ability to model atmosphere-ocean exchange of Hg, through more realistic ocean circulation from the 3-D MITgcm. Our results suggest Br is the dominant oxidant in the stratosphere, consistent with constraints from aircraft observations of the Hg gradient with depth into the stratosphere. The proposed redox mechanism leads to increased HgII deposition to the Tropics, with implications for tropical surface ocean enrichment, and decreased deposition to the Southern Ocean. Within the uncertainty of Hg0 oxidation rates, we find atmospheric HgII reduction is still needed. We find changes in speciated Hg emissions due to emissions controls can explain recent observed regional trends in atmospheric Hg. These have shifted power plant impacts to relatively more global than local Hg deposition. Coupling to the more realistic 3-D ocean model improves simulated atmospheric Hg

  13. HgL(3) XANES Study of Mercury Methylation in Shredded Eichhornia Crassipes

    Energy Technology Data Exchange (ETDEWEB)

    Rajan, M.; Darrow, J.; Hua, M.; Barnett, B.; Mendoza, M.; Greenfield, B.K.; Andrews, J.C.

    2009-05-21

    Eichhornia crassipes (water hyacinth) is a non-native plant found in abundance in the Sacramento-San Joaquin River Delta (hereafter called Delta). This species has become a problem, clogging waterways and wetlands. Water hyacinth are also known to accumulate mercury. Recent attempts to curb its proliferation have included shredding with specialized boats. The purpose of this research is to better understand the ability of water hyacinth to phytoremediate mercury and to determine the effect of shredding and anoxic conditions on mercury speciation in plant tissue. In the field assessment, total mercury levels in sediment from the Dow Wetlands in the Delta were found to be 0.273 {+-} 0.070 ppm Hg, and levels in hyacinth roots and shoots from this site were 1.17 {+-} 0.08 ppm and 1.03 {+-} 0.52 ppm, respectively, indicating bioaccumulation of mercury. Plant samples collected at this site were also grown in nutrient solution with 1 ppm HgCl{sub 2} under (1) aerobic conditions, (2) anaerobic conditions, and (3) with shredded plant material only. The greatest accumulation was found in the roots of whole plants. Plants grown in these conditions were also analyzed at Stanford Synchrotron Radiation Laboratory using Hg L{sub 3} X-ray Absorption Near Edge Spectroscopy (XANES), a method to examine speciation that is element-specific and noninvasive. Least-squares fitting of the XANES data to methylated and inorganic mercury(II) model compounds revealed that in plants grown live and aerobically, 5 {+-} 3% of the mercury was in the form of methylmercury, in a form similar to methylmercury cysteine. This percentage increased to 16 {+-} 4% in live plants grown anaerobically and to 22 {+-} 6% in shredded anaerobic plants. We conclude that shredding of the hyacinth plants and, in fact, subjection of plants to anaerobic conditions (e.g., as in normal decay, or in crowded growth conditions) increases mercury methylation. Mechanical removal of the entire plant is significantly more

  14. A study on removal of elemental mercury in flue gas using fenton solution

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Yangxian; Wang, Yan; Wang, Qian; Pan, Jianfeng [School of Energy and Power Engineering, Jiangsu University, Zhenjiang, Jiangsu 212013 (China); Zhang, Yongchun [Jiangsu Province Special Equipment Safety Supervision Inspection Institute (Branch of Wuxi), Wuxi 214000 (China); Zhou, Jianfei [School of Energy and Power Engineering, Jiangsu University, Zhenjiang, Jiangsu 212013 (China); Zhang, Jun [Key Laboratory of Energy Thermal Conversion and Control of Ministry of Education, Southeast University, Nanjing 210096 (China)

    2015-07-15

    Highlights: • A novel technique on oxidation of Hg{sup 0} using Fenton was proposed. • The effects of several process parameters on Hg{sup 0} removal were studied. • Products and ·OH in solution were detected. • Reaction mechanism of Hg{sup 0} removal was studied. • Simultaneous removal of Hg{sup 0}, NO and SO{sub 2} was also studied. - Abstract: A novel technique on oxidation-separation of elemental mercury (Hg{sup 0}) in flue gas using Fenton solution in a bubbling reactor was proposed. The effects of several process parameters (H{sub 2}O{sub 2} concentration, Hg{sup 0} inlet concentration, Fe{sup 2+} concentration, solution temperature, solution pH, gas flow) and several flue gas components (NO, SO{sub 2}, O{sub 2}, CO{sub 2}, inorganic ions and particulate matters on Hg{sup 0} removal were studied. The results indicate that H{sub 2}O{sub 2} concentration, Fe{sup 2+} concentration, solution pH and gas flow have great effects on Hg{sup 0} removal. Solution temperature, Hg{sup 0}, NO, SO{sub 2}, CO{sub 3}{sup 2−} and HCO{sub 3}{sup −} concentrations also have significant effects on Hg{sup 0} removal. However, Cl{sup −}, SO{sub 4}{sup 2−}, NO{sub 3}{sup −}, O{sub 2} and CO{sub 2} concentrations only have slight effects on Hg{sup 0} removal. Furthermore, reaction mechanism of Hg{sup 0} removal and simultaneous removal process of Hg{sup 0}, NO and SO{sub 2} were also studied. Hg{sup 0} is removed by oxidation of ·OH and oxidation of H{sub 2}O{sub 2}. The simultaneous removal efficiencies of 100% for SO{sub 2}, 100% for Hg{sup 0} and 88.3% for NO were obtained under optimal test conditions. The results demonstrated the feasibility of Hg{sup 0} removal and simultaneous removal of Hg{sup 0}, SO{sub 2} and NO using Fenton solution in a bubbling reactor.

  15. 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.

  16. MBE (Molecular Beam Epitaxial) growth characterization and electronic device processing of HgCdTe, HgZnTe related heterojunctions and HgCdTe-CdTe superlattices

    Science.gov (United States)

    Faurie, Jean-Pierre

    1987-06-01

    As the MBE growth technique has continued to improve for Hg(1-x)Cd(x)Te films, the prospects for films of larger area have begun to be explored. These larger area films are important for imaging arrays and will be especially vital in the future for the efficient production of Hg(1-x)Cd(x)Te material. The growth of MBE of uniform Hg(1-x)Cd(x)Te epilayer on a large substrate is very difficult to achieve because of the non-uniform distribution of the fluxes and on the non-uniform temperature of the substrate.

  17. A new method for oxidation of gaseous, elemental mercury.

    Energy Technology Data Exchange (ETDEWEB)

    Livengood, C. D.; Mendelsohn, M. H.

    1999-08-23

    Elemental mercury (Hg) is difficult to remove from flue-gas streams using existing wet-scrubber technology, primarily because of its limited volubility in water. We have proposed and tested a concept for enhancing gaseous Hg{sup 0}removal in wet scrubber systems by altering the chemical form of the Hg{sup 0} to a water-soluble oxidized species. Recently, we have discovered a new method for injection of the oxidizing species that dramatically improves reactant utilization and at the same time gives significant nitric oxide (NO) oxidation as well. Our method uses a diluted oxidizing solution containing chloric acid and sodium chlorate (sold commercially as NOXSORB{trademark}). When this solution is injected into a gas stream containing Hg{sup 0} at about 300 F, we found that nearly 100% of the Hg{sup 0} was removed from the gas phase and was recovered in liquid samples from the test system. At the same time, approximately 80% of the added NO was also removed (oxidized). The effect of sulfur dioxide (SO{sub 2}) on this method was also investigated, and it appears to decrease slightly the amount of Hg oxidized. We are currently testing the effect of variations in oxidizing solution concentration, SO{sub 2} concentration, NO concentration, and reaction time (residence time).

  18. Elemental Mercury Diffusion Processes and Concentration at the Lunar Poles

    Science.gov (United States)

    Moxley, Frederick; Killen, Rosemary M.; Hurley, Dana M.

    2011-01-01

    In 2009, the Lyman Alpha Mapping Project (LAMP) spectrograph onboard the Lunar Reconnaissance Orbiter (LRO) spacecraft made the first detection of element mercury (Hg) vapor in the lunar exosphere after the Lunar Crater Observing and Sensing Satellite (LCROSS) Centaur rocket impacted into the Cabeus crater in the southern polar region of the Moon. The lunar regolith core samples from the Apollo missions determined that Hg had a devolatilized pattern with a concentration gradient increasing with depth, in addition to a layered pattern suggesting multiple episodes of burial and volatile loss. Hg migration on the lunar surface resulted in cold trapping at the poles. We have modeled the rate at which indigenous Hg is lost from the regolith through diffusion out of lunar grains. We secondly modeled the migration of Hg vapor in the exosphere and estimated the rate of cold-trapping at the poles using a Monte Carlo technique. The Hg vapor may be lost from the exosphere via ionization, Jeans escape, or re-impact into the surface causing reabsorption.

  19. A preliminary study of the Hg flux from selected Ohio watersheds to Lake Erie

    International Nuclear Information System (INIS)

    New measurements of riverine dissolved and particulate Hg fluxes into Lake Erie from 12 northern Ohio watersheds have been determined from samples collected in April 2002 and analyzed using ultra-clean techniques with cold-vapor atomic fluorescence spectrometry. Total Hg concentrations ranged through 2.5-18.5 ng L-1, with a mean of 10.4 ng L-1 with most Hg in particulate form. Dissolved Hg concentrations ranged through 0.8-4.3 ng L-1, with a mean of 2.5 ng L-1. Highest total Hg concentrations were observed in western rivers with primarily agricultural land use and eastern rivers with mixed land use in their watersheds. Total suspended solid concentrations ranged through 10-180 mg L-1 with particulate Hg concentrations ranging through 47-170 ng g-1, with a mean of 99 ng g-1. Particulate Hg was similar to published data for central Lake Erie bottom sediments but much lower than for bottom sediments in western Lake Erie. Total Hg concentrations were positively correlated with suspended sediment concentrations and negatively with dissolved NO3- concentrations. The total estimated annual Hg fluxes from these rivers into Lake Erie is estimated to be 85 kg, but because only one event was sampled during high flow conditions, this may be an overestimate. This is much lower than previous published estimates of riverine Hg input into Lake Erie

  20. Body burden of Hg in different bio-samples of mothers in Shenyang city, China.

    Directory of Open Access Journals (Sweden)

    Min-Ming Li

    Full Text Available Hg is an accumulative and neuro-toxic heavy metal which has a wide range of adverse effects in human health. However, few studies are available on body burden of Hg level in different bio-samples of pregnant women in Chinese population. Therefore, this study evaluated Hg levels in different maternal bio-samples in Shenyang city, China and investigated the correlation of Hg levels in different bio-samples. From October to December 2008, 200 pregnant women about to deliver their babies at ShengJing Hospital (Shenyang city, northeast of China participated in this study. The geometric mean (GM of Hg levels in cord blood, maternal venous blood, breast milk, and maternal urine were 2.18 µg/L, 1.17 µg/L, 1.14 µg/L, and 0.73 µg/L, respectively, and the GM of maternal hair Hg level was 404.45 µg/kg. There was a strong correlation between cord blood and maternal blood total Hg level (r = 0.713, P<0.001. Frequency of fish consumption more than or equal to 3 times per week during pregnancy was suggested as a significant risk factor of prenatal Hg exposure (unadjusted OR 3.5, adjusted OR 2.94, P<0.05. This study provides evidence about Hg burden of mothers and the risk factors of prenatal Hg exposure in Shenyang city, China.

  1. Wading bird guano contributes to Hg accumulation in tree island soils in the Florida Everglades

    International Nuclear Information System (INIS)

    Tree islands are habitat for wading birds and a characteristic landscape feature in the Everglades. A total of 93 surface soil and 3 soil core samples were collected from 7 degraded/ghost and 34 live tree islands. The mean Hg concentration in surface soils of ghost tree islands was low and similar to marsh soil. For live tree islands, Hg concentrations in the surface head region were considerably greater than those in mid and tail region, and marsh soils. Hg concentrations in bird guano (286 μg kg−1) were significantly higher than those in mammal droppings (105 μg kg−1) and plant leaves (53 μg kg−1). In addition, Hg concentrations and δ15N values displayed positive correlation in soils influenced by guano. During 1998–2010, estimated annual Hg deposition by guano was 148 μg m−2 yr−1 and ∼8 times the atmospheric deposition. Highlights: • Hg concentrations in the head region of tree islands were the highest. • Hg concentrations in bird guano (286 μg kg−1) were significantly higher than those in mammal droppings and plant leaves. • Hg concentrations and δ15N values showed positive correlation in soils influenced by guano. • Estimated annual Hg deposition by guano was 148 μg m−2 yr−1, ∼8 times the atmospheric deposition. -- The annual Hg deposition by bird guano to tree island soils in the Everglades was ∼8 times the atmospheric deposition

  2. Application of residual sludge: effects on soil nitrogen and retention of Cd, Cr, Hg and Zn by ray grass

    International Nuclear Information System (INIS)

    In pot studies on the application of urban sewage rich in organic matter as fertilizer (residual sludges from sewage purification stations), an investigation was made of the yield in dry matter and retention of Zn, Cd, Cr and Hg by ray grass, followed by an examination of the mineralization and organization of soil nitrogen or added nitrogen fertilizers. All the experiments described were conducted with tracers - radioactive in the case of Hg, Cd, Cr and Zn, and stable in the case of nitrogen. The main results obtained after six months' cultivation can be summarized as follows: (1) the suppressing effect produced immediately after application of a lime-treated sludge falls off rapidly (2-3 months), whereas the effect produced by straw persists even after six months. The sludges subsequently exert a positive effect on the yield of dry matter; (2) in the plant the transfer of the trace elements studied is not altered by adding residual sludges whereas the addition of 30 ppm of these elements to the soil in ionic form increases the plant content; (3) although the incorporation of straw into the soil considerably increases the organization of the nitrogen in the fertilizer applied, the changes are limited in the case of other forms of treatment. (author)

  3. PELTIER ELEMENTS

    CERN Document Server

    Tani, Laurits

    2015-01-01

    To control Peltier elements, temperature controller was used. I used TEC-1091 that was manufactured my Meerstetter Engineering. To gain control with the temperature controller, software had to be intalled on a controlling PC. There were different modes to control the Peltier: Tempererature controller to control temperature, Static current/voltage to control voltage and current and LIVE ON/OFF to auto-tune the controller respectively to the system. Also, since near the collision pipe there is much radiation, radiation-proof Peltier elements have to be used. To gain the best results, I had to find the most efficient Peltier elements and try to get their cold side to -40 degrees Celsius.

  4. Study on the application of cold vapor atomic absorption spectrometry and hydride generation atomic absorption spectrometry for the determination of Hg and As traces in sea water samples

    International Nuclear Information System (INIS)

    The trace amount of total mercury (Hg) and arsenic (As) in sea water samples were quantitatively determined by using the Atomic Absorption Spectrometry connected with the hydride generation technique (HG-AAS) for As, and with the cold vapour technique (CV-AAS) for Hg. The experiments were carried out at room temperature on a Hydride System Module (HS55) combined with an Atomic Absorption Spectrometer (VARIO 6, Analytik Jena AG). The effect of reductants concentration, and that of matrix on the absorption intensity of each analyzed element was studied in details. The sea water sample after fitrating through a membrane with 0.45(μm-hole size was pre-treated with an oxidant or an reductant to obtain the identical medium. The absorption intensity of each element was then measured on the VARIO-6 under the optimum parameters for spectrometer such as: maximum wavelength, current of hollow cathode lamp, and that for hydride system such as cell temperature, speed of peristaltic pump, pump time, reaction time and rewash time, ect. The analytical procedures were set-up and applied for the determination of these above mentioned elements in the synthesized sea water sample and in the real sea water samples with high precision and accuracy. (author)

  5. Feasibility study on the use of soil washing to remediate the As-Hg contamination at an ancient mining and metallurgy area.

    Science.gov (United States)

    Sierra, C; Menéndez-Aguado, J M; Afif, E; Carrero, M; Gallego, J R

    2011-11-30

    Soils in abandoned mining sites generally present high concentrations of trace elements, such as As and Hg. Here we assessed the feasibility of washing procedures to physically separate these toxic elements from soils affected by a considerable amount of mining and metallurgical waste ("La Soterraña", Asturias, NW Spain). After exhaustive soil sampling and subsequent particle-size separation via wet sieving, chemical and mineralogical analysis revealed that the finer fractions held very high concentrations of As (up to 32,500 ppm) and Hg (up to 1600 ppm). These elements were both associated mainly with Fe/Mn oxides and hydroxides. Textural and geochemical data were correlated with the geological substrate by means of a multivariate statistical analysis. In addition, the Hg liberation size (below 200 μm) was determined to be main factor conditioning the selection of suitable soil washing strategies. These studies were finally complemented with a specific-gravity study performed with a C800 Mozley separator together with a grindability test, both novel approaches in soil washing feasibility studies. The results highlighted the difficulties in treating "La Soterraña" soils. These difficulties are attributed to the presence of contaminants embedded in the soil and spoil heap aggregates, caused by the meteorization of gangue and ore minerals. As a result of these two characteristics, high concentrations of the contaminants accumulate in all grain-size fractions. Therefore, the soil washing approach proposed here includes the grinding of particles above 125 μm.

  6. A Novel Sample Introduction Technique for the Simultaneous Determination of As, Se, Ge and Hg in Chinese Medicinal Material

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    A novel technique of Moveable Reduction Bed Hydride Generator(MRBHG) was applied to the hydride generation or cold vapor generation of As, Se, Ge, and Hg existing in Traditional Chinese Medicinal Material(TCM). The simultaneous determination of the multi-elements was performed with ICP-MS. A solid reduction system involving the use of potassium tetraborohydride and tartaric acid was applied to generating metal hydride or cold vapor efficiently. The factors affecting the metal cold vapor generation were studied. The main advantage of the technique is that only a 4 μL volume of sample was required for the cold vapor generation. The absolute detection limits of all the elements studied are in 10-12 g level.

  7. Multiconfiguration Dirac-Hartree-Fock calculations of atomic electric dipole moments of 225^Ra, 199^Hg, and 171^Yb

    CERN Document Server

    Radziute, Laima; Jonsson, Per; Biero, Jacek

    2013-01-01

    The multiconfiguration Dirac-Hartree-Fock (MCDHF) method has been employed to calculate atomic electric dipole moments (EDM) of 225^Ra, 199^Hg, and 171^Yb. For the calculations of the matrix elements we extended the relativistic atomic structure package GRASP2K. The extension includes programs to evaluate matrix elements of (P, T)-odd e-N tensor-pseudotensor and pseudoscalar-scalar interactions, the atomic electric dipole interaction, the nuclear Schiff moment, and the interaction of the electron electric dipole moment with nuclear magnetic moments. The interelectronic interactions were accounted for through valence and core-valence electron correlation effects. The electron shell relaxation was included with separately optimised wave functions of opposite parities.

  8. Radiographic element

    International Nuclear Information System (INIS)

    Radiographic elements are disclosed having first and second silver halide emulsion layers comprised of a dispersing medium and radiation-sensitive silver halide grains, and a support interposed between said silver halide emulsion layers capable of transmitting radiation to which said second silver halide emulsion layer is responsive. These elements are characterized in that at least said first silver halide emulsion layer contains tabular silver halide grains and spectral sensitizing dye adsorbed to the surface of the grains. Crossover can be improved in relation to the imaging characteristics. (author)

  9. [HG-AFS determination of selenium in Moringa oleifera].

    Science.gov (United States)

    Huang, Guo-qing; Xiao, Zi-jun

    2007-02-01

    The Se content in Moringa oleifera was studied by hydride generation atom fluorescence spectrometry (HG-AFS) with wet digestion. The effects of the way of digestion, the work condition of apparatus, the reaction medium and acidity, and the reducing agent and masking agent on the determination of Se were investigated. And the operating condition of apparatus was optimized. The results showed that the detection limit of Se in this method was 0.42 ng x mL(-1) in the linear ranger of 0-120 ng x mL(-1), the relative standard deviation was 3.53% (n = 11), and the recovery of the method was 95.2%-104.6%. It was showed that the method was very sensitive, simple, rapid and accurate.

  10. Lifetimes of an excited superdeformed band in {sup 192}Hg

    Energy Technology Data Exchange (ETDEWEB)

    Ahmad, I.; Blumenthal, D.; Carpenter, M.P. [and others

    1995-08-01

    An excited superdeformed band was identified in {sup 192}Hg and the lifetimes of its levels measured with the Doppler-shift attenuation method from data taken with the Eurogam spectrometer. The band is proposed to be based on the two-quasineutron (v[642]3/2 [512]5/2) configuration, which after a band crossing, becomes the (v[642]3/2 [752]5/2) configuration. The transition quadrupole moment Q{sub t} of the excited band is the same as that of the yrast SD band, within experimental errors. This suggests that the deformation of the SD minimum is robust with respect to quasiparticle excitation, despite the occupation of the deformation-driving v[752]5/2 level (from the j{sub 15/2} shell) after the band crossing.

  11. Thomson scattering on high pressure Hg discharge lamps

    Energy Technology Data Exchange (ETDEWEB)

    Zhu, X [Department of Applied Physics, Eindhoven University of Technology, PO Box 513, 5600 MB, Eindhoven (Netherlands); Vries, N de [Department of Applied Physics, Eindhoven University of Technology, PO Box 513, 5600 MB, Eindhoven (Netherlands); Kieft, E R [Department of Applied Physics, Eindhoven University of Technology, PO Box 513, 5600 MB, Eindhoven (Netherlands); Mullen, J J A M van der [Department of Applied Physics, Eindhoven University of Technology, PO Box 513, 5600 MB, Eindhoven (Netherlands); Haverlag, M [Department of Applied Physics, Eindhoven University of Technology, PO Box 513, 5600 MB, Eindhoven (Netherlands); Central Development Lighting, Philips Lighting, PO Box 80020, 5600 JM, Eindhoven (Netherlands)

    2005-06-21

    Thomson scattering (TS) experiments have been performed on high-pressure Hg discharge lamps. These lamps were filled with different amounts of Hg (15, 30, 50 and 70 mg) and were operating at different powers (150, 200 and 240 W) with a square-wave ballast. As in the previous studies (Zhu X et al 2004 J. Phys. D: Appl. Phys. 37 736-43) a triple grating spectrograph was used to suppress the false stray light and Rayleigh scattered photons. This set-up had to be modified for this special application. The collective TS spectra have been fitted using both a calibration using Raman scattering and a form fitting procedure. It was found that the electron temperature fluctuates around a certain value that seems rather constant in the central region. The value of electron temperature (T{sub e}) varies between 5500 and 7600 K in the central region (r {<=} 0.3 R). The spatial-averaged T{sub e} value increases with the lamp power. The electron density was found to be of the order of 10{sup 21} m{sup -3} which is high at the centre and decreases as r increases. The n{sub e} value also increases with the lamp power. Moreover the results of TS are compared with those from x-ray absorption measurement. The comparison shows that the plasmas in such lamps are not in local thermal equilibrium in the sense that T{sub e} {ne} T-dot{sub g}-gas temperature and locally the rate of ionization is much larger than that of three body recombination.

  12. 201Hg excitation in plasma produced by laser

    International Nuclear Information System (INIS)

    The use of high power lasers allows the study of the properties of matter in extreme conditions of temperature and density. Indeed, the interaction of a power laser and a target creates a plasma in which the temperature is high enough to reach important degrees of ionization. These conditions can allow the excitation of the nucleus. A nucleus of interest to study the processes of nuclear excitation is the 201Hg. This work aims to design an experiment where the 201Hg excitation will be observed in a plasma produced by a high power laser. The first part of this manuscript presents the calculation of the expected nuclear excitation rates in the plasma. For about ten years, nuclear excitation rates have been calculated using the average atom model. To validate this model a code named ADAM (French acronym for Beyond The Average Atom Model) was developed to calculate the nuclear excitation rates under the DCA (Detailed Configuration Accounting) hypothesis. ADAM allows us to deduce the thermo dynamical domain where the nuclear excitation rates determined with the average atom model are relevant. The second part of this manuscript presents the coupling of the excitation rate calculation with a hydrodynamic code to calculate the number of excited nuclei produced in one laser shot for different laser intensity. Finally, in the last part, first experimental approaches which will be used to design an experiment on a laser installation are presented. These approaches are based on the detection and determination of the amount of multicharged ions obtained far from the target (∼80 cm). For this purpose, an electrostatic analyzer was used. (author)

  13. Global observations and modeling of atmosphere-surface exchange of elemental mercury: a critical review

    Science.gov (United States)

    Zhu, Wei; Lin, Che-Jen; Wang, Xun; Sommar, Jonas; Fu, Xuewu; Feng, Xinbin

    2016-04-01

    Reliable quantification of air-surface fluxes of elemental Hg vapor (Hg0) is crucial for understanding mercury (Hg) global biogeochemical cycles. There have been extensive measurements and modeling efforts devoted to estimating the exchange fluxes between the atmosphere and various surfaces (e.g., soil, canopies, water, snow, etc.) in the past three decades. However, large uncertainties remain due to the complexity of Hg0 bidirectional exchange, limitations of flux quantification techniques and challenges in model parameterization. In this study, we provide a critical review on the state of science in the atmosphere-surface exchange of Hg0. Specifically, the advancement of flux quantification techniques, mechanisms in driving the air-surface Hg exchange and modeling efforts are presented. Due to the semi-volatile nature of Hg0 and redox transformation of Hg in environmental media, Hg deposition and evasion are influenced by multiple environmental variables including seasonality, vegetative coverage and its life cycle, temperature, light, moisture, atmospheric turbulence and the presence of reactants (e.g., O3, radicals, etc.). However, the effects of these processes on flux have not been fundamentally and quantitatively determined, which limits the accuracy of flux modeling. We compile an up-to-date global observational flux database and discuss the implication of flux data on the global Hg budget. Mean Hg0 fluxes obtained by micrometeorological measurements do not appear to be significantly greater than the fluxes measured by dynamic flux chamber methods over unpolluted surfaces (p = 0.16, one-tailed, Mann-Whitney U test). The spatiotemporal coverage of existing Hg0 flux measurements is highly heterogeneous with large data gaps existing in multiple continents (Africa, South Asia, Middle East, South America and Australia). The magnitude of the evasion flux is strongly enhanced by human activities, particularly at contaminated sites. Hg0 flux observations in East

  14. Characterization of the native defects in HgTe, CdTe, Hg1-x, CdxTe by positron annihilation: evidence of native vacancies

    International Nuclear Information System (INIS)

    Direct evidence of native vacancies is found in as-grown CdxHg1-xTe single crystals prepared by the travelling heating method (THM). The vacancies have characteristics depending on the annealing undergone by the crystals after their growth and on the conduction type in the crystals. In as-grown CdTe and Cd0.7Hg0.3Te (THM), native vacancies are found in n-type materials. In as-grown HgTe and Cd0.2Hg0.8Te (THM), native vacancies are found in p materials. They disappear after stoechiometric annealings in which the crystals are converted n-type. From the positron lifetime at the vacancies, 320±4 ps, one can show that the native vacancies are metallic vacancies VCd in CdTe, VHg in HgTe, VHg or/and VCd in CdxHg1-xTe alloys. The concentration of the metallic vacancies is estimated in as-grown crystals. In as-grown p-type CdTe and Cd0.7Hg0.3Te (THM), in as-grown then subsequently p-type annealed HgTe and Cd0.2Hg0.8Te (THM), vacancy type defects are also found giving rise to lifetime of about 290 ps. These defects are also found in crystals grown by Bridgman method. The nature of these defects is discussed. The In doping effects on the metallic vacancies have been studied. It is shown that In addition increases the concentration of metallic vacancies in CdTe (In) (THM). Vacancy-In complexes appear for In concentrations of the order or above 1017 cm-3. These complexes disappear after decompensating annealings and only the metallic vacancies survive. Small vacancies clusters of two or three vacancies are found after deformation at room temperature in CdTe (Mn) (THM)

  15. Excitation spectra and ground-state properties from density functional theory for the inverted band-structure systems $\\beta$-HgS, HgSe, and HgTe

    CERN Document Server

    Delin, A

    2002-01-01

    We have performed a systematic density-functional study of the mercury chalcogenide compounds $\\beta$-HgS, HgSe, and HgTe using an all-electron full-potential linear muffin-tin orbital (FP-LMTO) method. We find that, in the zinc-blende structure, both HgSe and HgTe are semimetals whereas $\\beta$-HgS has a small spin-orbit induced band gap. Our calculated relativistic photoemission and inverse photoemission spectra (PES and IPES, respectively) reproduce very well the most recently measured spectra, as do also our theoretical optical spectra. In contrast to the normal situation, we find that the local density approximation (LDA) to the density functional gives calculated equilibrium volumes in much better agreement with experiment than does the generalized gradient corrected functional (GGA). We also address the problem of treating relativistic $p$ electrons with methods based on a scalar-relativistic basis set, and show that the effect is rather small for the present systems.

  16. Sediment accumulation and mercury (Hg) flux in Avicennia marina forest of Deep Bay, China

    Science.gov (United States)

    Li, Ruili; Chai, Minwei; Guo, Meixian; Qiu, Guo Yu

    2016-08-01

    To investigate the rate of sediment accumulation and mercury (Hg) flux in Avicennia marina forest of Deep Bay, China, sediment cores were analyzed. The results showed that Hg concentrations were much higher at all depths compared to the background level. A high correlation between Hg and total organic carbon (TOC) indicated their similar anthropogenic origin. Sedimentation rate was estimated to be 1.38 cm a-1 by 210Pb geochronology. The increase in the mass sediment accumulation rates was rapid (range: 0.5-0.94 g cm-2 a-1), and the Hg fluxes ranged between 76 and 116 ng cm-2 a-1 during the last three decades. The reduction in both Hg concentrations and flux during the last decade may be due to the adoption of contamination control policies. Our results support the notion that the Hg fluxes determined from the sediment cores reveal the effects of anthropogenic influences from the areas around Deep Bay.

  17. Stability studies of Hg implanted YBa$_{2}$Cu$_{3}$O$_{6+x}$

    CERN Document Server

    Araújo, J P; Wahl, U; Marques, J G; Alves, E; Amaral, V S; Lourenço, A A; Galindo, V; Von Papen, T; Senateur, J P; Weiss, F; Vantomme, A; Langouche, G; Melo, A A; Da Silva, M F A; Soares, J C; Sousa, J B

    1999-01-01

    High quality YBa$_{2}$Cu$_{3}$O$_{6+x}$ (YBCO) superconducting thin films were implanted with the radioactive $^{197m}$Hg (T$_{1/2}$ = 24 h) isotope to low fluences of 10$^{13}$ atoms/cm$^{2}$ and 60 keV energy. The lattice location and stability of the implanted Hg were studied combining the Perturbed Angular Correlation (PAC) and Emission Channeling (EC) techniques. We show that Hg can be introduced into the YBCO lattice by ion implantation into unique regular sites. The EC data show that Hg is located on a highly symmetric site on the YBCO lattice, while the PAC data suggests that Hg occupies the Cu(1) site. Annealing studies were performed under vacuum and O$_{2}$ atmosphere and show that Hg starts to diffuse only above 653 K.

  18. Admittance Investigation of MIS Structures with HgTe-Based Single Quantum Wells.

    Science.gov (United States)

    Izhnin, Ihor I; Nesmelov, Sergey N; Dzyadukh, Stanislav M; Voitsekhovskii, Alexander V; Gorn, Dmitry I; Dvoretsky, Sergey A; Mikhailov, Nikolaj N

    2016-12-01

    This work presents results of the investigation of admittance of metal-insulator-semiconductor structure based on Hg1 - x Cd x Te grown by molecular beam epitaxy. The structure contains a single quantum well Hg0.35Cd0.65Te/HgTe/Hg0.35Cd0.65Te with thickness of 5.6 nm in the sub-surface layer of the semiconductor. Both the conductance-voltage and capacitance-voltage characteristics show strong oscillations when the metal-insulator-semiconductor (MIS) structure with a single quantum well based on HgTe is biased into the strong inversion mode. Also, oscillations on the voltage dependencies of differential resistance of the space charge region were observed. These oscillations were related to the recharging of quantum levels in HgTe. PMID:26831691

  19. Electro-physical characteristics of MIS structures with HgTe- based single quantum wells

    Science.gov (United States)

    Dzyadukh, S.; Nesmelov, S.; Voitsekhovskii, A.; Gorn, D.

    2015-12-01

    The paper presents brief research results of the admittance of metal-insulator- semiconductor (MIS) structures based on Hg1-xCdxTe grown by molecular-beam epitaxy (MBE) method including single HgCdTe/HgTe/HgCdTe quantum wells (QW) in the surface layer. The thickness of a quantum well was 5.6 nm, and the composition of barrier layers with the thickness of 35 nm was close to 0.65. Measurements were conducted in the range of temperatures from 8 to 200 K. It is shown that for structure with quantum well based on HgTe capacitance and conductance oscillations in the strong inversion are observed. Also it is assumed these oscillations are related with the recharging of quantum levels in HgTe.

  20. Food preferences and Hg distribution in Chelonia mydas assessed by stable isotopes.

    Science.gov (United States)

    Bezerra, M F; Lacerda, L D; Rezende, C E; Franco, M A L; Almeida, M G; Macêdo, G R; Pires, T T; Rostán, G; Lopez, G G

    2015-11-01

    Mercury (Hg) is a highly toxic pollutant that poses in risk several marine animals, including green turtles (Chelonia mydas). Green turtles are globally endangered sea turtle species that occurs in Brazilian coastal waters as a number of life stage classes (i.e., foraging juveniles and nesting adults). We assessed total Hg concentrations and isotopic signatures ((13)C and (15)N) in muscle, kidney, liver and scute of juvenile green turtles and their food items from two foraging grounds with different urban and industrial development. We found similar food preferences in specimens from both areas but variable Hg levels in tissues reflecting the influence of local Hg backgrounds in food items. Some juvenile green turtles from the highly industrialized foraging ground presented liver Hg levels among the highest ever reported for this species. Our results suggest that juvenile foraging green turtles are exposed to Hg burdens from locally anthropogenic activities in coastal areas. PMID:26196313

  1. ELECTRON TRANSFER IN Hg1-xCdxTe-CdTe HETEROSTRUCTURES

    OpenAIRE

    Boebinger, G.; Vieren, J.; Guldner, Y.; Voos, M.; Faurie, J.

    1987-01-01

    Far infrared magneto-absorption experiments performed at 1.6K in HgCdTe-CdTe heterojunctions show that a two-dimensional electron gas is formed in the HgCdTe layer at the HgCdTe-CdTe interface. The electron effective masses of the two populated subbands is obtained and compared to previous theoretical calculations. The electron transfer across the interface involves deep traps in the CdTe layers.

  2. Some health physics aspects of working with 203Hg in university research.

    Science.gov (United States)

    Belanger, M; Westin, A; Barfuss, D W

    2001-02-01

    The radioisotope 203Hg is used in university toxicology research experiments. When our commercial vendor ceased the production of the high specific activity 203Hg we required, an alternative source was sought. Other commercial sources were investigated without success leaving the synthesis of this radioisotope to us. This paper outlines the method we used to synthesize 203Hg and provides a summary of our results to date and a discussion of our experiences.

  3. Effects of Gravity on the Double-Diffusive Convection during Directional Solidification of a Non-Dilute Alloy with Application to the HgCdTe

    Science.gov (United States)

    Bune, Andris; Gillies, Donald; Lehoczky, Sandor

    1999-01-01

    General 2-D and 3-D finite element model of non-dilute alloy solidification was used to simulate growth of HgCdTe in terrestrial and microgravity conditions. Parametric research was undertaken to investigate effects of gravity level, gravity vector orientation and growth velocity on the pattern of melt convection, shape of crystal/melt interface and radial thermal gradient. Verification of the model was undertaken by comparison with previously published results. For low growth velocities plane front solidification occurs. The location and the shape of the interface was determined using melting temperatures obtained from the HgCdTe liquidus curve. The low thermal conductivity of the solid HgCdTe causes thermal short circuit through the ampoule walls, resulting in curved isotherms in the vicinity of the interface. Double-diffusive convection in the melt is caused by radial temperature gradients and by material density inversion with temperature. Cooling from below and the rejection at the solid-melt interface of the heavier HgTe-rich solute each tend to reduce convection. Because of these complicating factors dimensional rather then non-dimensional modeling was performed. For gravity levels higher then 10(exp -7) of terrestrial one it was found that the maximum convection velocity is extremely sensitive to gravity vector orientation and can be reduced at least by 50% by choosing proper orientation of the ampoule. The predicted interface shape is in agreement with one obtained experimentally by quenching.

  4. Effects of Gravity on the Double-Diffusive Convection During Directional Solidification of a Non-Dilute Alloy with Application to HgCdTe

    Science.gov (United States)

    Bune, Andris V.; Gillies, Donald C.; Lehoczky, Sandor L.

    1999-01-01

    A general 2-D and 3-D finite element model of non-dilute alloy solidification was used to simulate growth of HgCdTe in terrestrial and microgravity conditions. Verification of the 3-D model was undertaken by comparison with previously published results on convection in an inclined cylinder. For low growth velocities, plane front solidification occurs. The location and the shape of the interface were determined using melting temperatures obtained from the HgCdTe liquidus curve. The low thermal conductivity of the solid HgCdTe causes a thermal short circuit through the ampoule walls, resulting in curved isotherms in the vicinity of the interface. Double-diffusive convection in the melt is caused by radial temperature gradients and by material density inversion due to the combined effects of composition and temperature. Cooling from below and the rejection at the solid-melt interface of the heavier HgTe-rich solute each tend to reduce convection. Because of these complicating factors, dimensional rather than non-dimensional modeling was performed. the predicted interface shape is in agreement with one obtained experimentally by quenching.

  5. Modification and characterization of PET fibers for fast removal of Hg(II), Cu(II) and Co(II) metal ions from aqueous solutions.

    Science.gov (United States)

    Monier, M; Abdel-Latif, D A

    2013-04-15

    A new chelating fiber (PET-TSC) was prepared with PET for fast removal of Hg(2+), Cu(2+) and Co(2+) from water. Elemental analysis, SEM, BET surface area, (13)C NMR, FTIR and X-ray diffraction spectra were used to characterize PET-TSC. The higher uptake capacity of the studied metal ions was observed at higher pH values. Kinetic study indicated that the adsorption of Hg(2+), Cu(2+) and Co(2+) followed the pseudo-second-order equation, suggesting chemical sorption as the rate-limiting step of the adsorption process. The best interpretation for the equilibrium data was given by Langmuir isotherm, and the maximum adsorption capacities were 120.02, 96.81 and 78.08 mg/g for Hg(2+), Cu(2+) and Co(2+) ions, respectively. 1M HCl or 0.1M EDTA could be used as effective eluant to desorb the Hg(2+), Cu(2+) and Co(2+) adsorbed by PET-TSC, and the adsorption capacity of PET-TSC for the three heavy metal ions could still be maintained at about 90% level at the 5th cycle. Accordingly, it is expected that PET-TSC could be used as a promising adsorbent for fast removal of heavy metal ions from water, and the present work also might provide a simple and effective method to reuse the waste PET fibers. PMID:23435202

  6. Trace and toxic elements in foodstuffs in Japan

    International Nuclear Information System (INIS)

    Concentrations of trace elements in several foodstuffs collected in Japan were analyzed by neutron activation analysis (NAA), inductively-coupled plasma atomic emission spectrometry (ICP-AES) and anodic striping voltametry (ASV). The elements analyzed were as follows: Zn, Se, As, Hg, Cs, Cr, Co, Fe, Rb, Br and K by NAA; Mn, Ba, Sr, Mg, Ca, P, K, Zn, Cu and Fe by ICP-AES; and Pb, Cd, Cu and Zn by ASV. Because of the high consumption of rice in Japan, the focus of analysis was on this foodstuff. Concentrations of K, Mg, Mn, P and Zn in different polished rice samples were similar, whereas those of Br, Co, Cs, Rb and Se varied. Levels of toxic elements in polished rice were generally lower than those in other foodstuffs. The highest concentrations of As, Hg, Se and Zn were found in marine products, i.e.. Hijiki-algae (As: 59 mg/kg, dry), tuna (Hg: 1.1 mg/kg, dry), bonito (Se: 4.5 mg/kg, dry) and oysters (Zn: 350 mg/kg, dry). Dietary intakes of As, Ca, Cd, Cu, Fe, Hg, K, Mg, Mn, P, Pb, Se and Zn by Japanese were estimated by using these analytical results and published food consumption data in Japan. We have also identified the major sources of the elements in dietary intakes as follows: (a) about 90% of the As was derived from marine products (fish and seaweed); (b) about 70% of the Hg was derived from fish; (c) about 40-60% of the Cd and the Mn and 20-40% of the Zn, Cu and Mg was derived from rice; (d) selenium was mostly derived from fish, meat and eggs; (e) more than 20% of the Ca was derived from milk and milk products; (f) elements such as Fe, K, P and Pb was derived from different sorts of foodstuffs. (author). 7 refs, 1 fig., 7 tabs

  7. Stoichiometry, thickness and crystallinity of MOCVD grown Hg1x-yCdxMnyTe determined by nuclear techniques of analysis

    International Nuclear Information System (INIS)

    The quaternary semi-conductor Hg1-x-yCdxMnyTe has been grown by Metal Organic Chemical Vapour Deposition using the Interdiffused Multi-layer Process. The layers have been analysed by Ion beam (PIXE, RBS, channeling) and related analytical techniques (EDXRF, XRD, RHEED) to obtain stoichiometric and structural information. The analysis shows that all four elements are present throughout the layer and that the elemental concentrations and thickness of the layer vary considerably over the film. Channeling, XRD and RHEED have been combined to show that the layer is polycrystalline. 14 refs., 3 figs

  8. Ultrasensitive and selective spectrofluorimetric determination of Hg(II) using a dimercaptothiadiazole fluorophore

    International Nuclear Information System (INIS)

    The present work describes the ultrasensitive and selective spectrofluorimetric determination of Hg(II) using 2,5-dimercaptothiadiazole (DMT) as a fluorophore. DMT shows an emission maximum at 435 nm while exciting at 330 nm. The colorless solution of DMT changes into a highly emittive yellow color immediately after the addition of 0.5 μM Hg(II) and nearly 245-fold increase in emission intensity at 435 nm was observed. These changes were ascribed to the complex formation between Hg(II) and DMT. Based on the fluorescence enhancement, the concentration of Hg(II) was determined. The binding constant value (KA=1.8620x104 mol-1 L) suggests that there is a strong binding force between Hg(II) and DMT. The fluorescence quantum yield of DMT-Hg(II) complex was found to be 4-fold higher than that of DMT, indicating that the DMT-Hg(II) complex was highly emittive than the DMT. Interestingly, the emission intensity was increased even in the presence of 0.1 pM Hg(II). The fluorophore showed an extreme selectivity towards 100 nM Hg(II) in the presence of 50,000-fold higher concentrations of Na+, K+, Ca2+, Mg2+, Fe2+, Fe3+, Cd2+, Cr3+, Mn2+, Zn2+, Co2+, Ni2+, Cl-, SO42-, NO3- ions and 1000-, 500- and 200-fold higher concentrations of Cu2+, Pb2+ and Ag+ ions, respectively, as interferences. The lowest detection of 18 pg L-1 Hg(II) (LOD=3S/m) was achieved for the first time using DMT by fluorimetry. The proposed method was successfully utilized for the determination of Hg(II) in tap water, river water and industrial waste water samples. - Highlights: → 2,5-Dimercpato-1,3,4-thiadiazole was used as a fluorophore for Hg(II) determination. → 245-Fold increase in emission intensity was observed after the addition of 0.5 μM Hg(II). → Using the present method, a detection limit of 18 p Hg(II) was achieved. → Hg(II) was determined in the presence of 50,000-fold concentrations of interferences. → The proposed method was utilized for the determination of Hg(II) in real samples.

  9. Effects of salinity and humic acid on the sorption of Hg on Fe and Mn hydroxides.

    Science.gov (United States)

    Liang, Peng; Li, Yi-Chun; Zhang, Chan; Wu, Sheng-Chun; Cui, Hao-Jie; Yu, Shen; Wong, Ming H

    2013-01-15

    The objective of this study was to investigate the influence of humic acid (HA) and salinity on adsorption of Hg on the amorphous and crystalline of iron and manganese hydroxides. The results show that the adsorption of Hg(2+) on Fe and Mn hydroxides was inhibited in marine system due to the formation of stable, nonsorbing aqueous HgCl(2) complexes in solution. Moreover, Cl(-) inhibited the Hg(2+) adsorption more severely on amorphous than crystalline hydroxides. The addition of HA inhibited Hg(2+) adsorption on Fe and Mn hydroxides in freshwater system might be attributed to the competition between Hg(2+) and HA on adsorption to Fe and Mn hydroxides. In contrast, the addition of HA promoted Hg(2+) adsorption on Fe and Mn hydroxides in the marine system, which might be due to the addition of humic acid resulted in the reaction between Cl(-) and HA, and therefore the reducing of Cl(-) promoted more Hg(2+) on Fe and Mn hydroxides. In addition, the influence of HA on Hg(2+) adsorption on Fe and Mn hydroxides are more visible for crystalline than amorphous hydroxides.

  10. Combined in-beam electron and gamma-ray spectroscopy of (184,186)Hg

    CERN Document Server

    Scheck, M; Rahkila, P; Butler, P A; Larsen, A C; Sandzelius, M; Scholey, C; Carrol, R J; Papadakis, P; Jakobsson, U; Grahn, T; Joss, D T; Watkins, H V; Juutinen, S; Bree, N; Cox, D; Huyse, M; Uusitalo, J; Leino, M; Ruotsalainen, P; Nieminen, P; Srebrny, J; Van Duppen, P; Herzan, A; Greenlees, P T; Julin, R; Herzberg, R D; Hauschild, K; Pakarinen, J; Page, R D; Peura, P; Gaffney, L P; Kowalczyk, M; Rinta-Antila, S; Saren, J; Lopez-Martens, A; Sorri, J; Ketelhut, S

    2011-01-01

    By exploiting the SAGE spectrometer a simultaneous measurement of conversion electrons and gamma rays emitted in the de-excitation of excited levels in the neutron-deficient nuclei (184,186)Hg was performed. The light Hg isotopes under investigation were produced using the 4n channels of the fusion-evaporation reactions of (40)Ar and (148,150)Sm. The measured K- and L-conversion electron ratios confirmed the stretched E2 nature of several transitions of the yrast bands in (184,186)Hg. Additional information on the E0 component of the 2(2)(+) -> 2(1)(+) transition in (186)Hg was obtained.

  11. Improved limit on the permanent electric dipole moment of 199Hg

    CERN Document Server

    Griffith, W C; Loftus, T H; Romalis, M V; Heckel, B R; Fortson, E N

    2009-01-01

    We report the results of a new experimental search for a permanent electric dipole moment of 199Hg utilizing a stack of four vapor cells. We find d(199Hg) = (0.49 \\pm 1.29_stat \\pm 0.76_syst) x 10^{-29} e cm, and interpret this as a new upper bound, |d(199Hg)| < 3.1 x 10^{-29} e cm (95% C.L.). This result improves our previous 199Hg limit by a factor of 7, and can be used to set new constraints on CP violation in physics beyond the standard model.

  12. Chemical stabilization of 1201-type Hg-Sr based cuprate superconductors

    International Nuclear Information System (INIS)

    The 1201-type Ba-free Hg-Sr based cuprate superconductors with nominal compositions of Hg1-xMoxSr2CuO4+δ(x=0.1-0.25) were synthesized and characterized. The 1201-type structure was stabilized by partial substitution of Mo in the Hg site. A typical composition, Hg0.85Mo0.15 Sr2CuO4+δ crystallizes in tetragonal structure with a=3.769 A and c=8.801 A and a superconducting transition of 57 K was measured. (author)

  13. Capability of Catfish (Clarias gariepinus to Accumulate Hg2+ From Water

    Directory of Open Access Journals (Sweden)

    Heny Suseno

    2015-12-01

    Full Text Available Mercury is hazardous contaminant that can be accumulated by aquatic organisms such as fishes, mussels etc. Catfish is one of source of animal protein but it also can accumulate Hg2+ from water that used in aquaculture. Due to less information about capability of catfish to accumulate Hg2+, therefore we studied bioaccumulation of Hg2+ that used biokinetic approach (aqueous uptake-rate, and elimination-rate.  Nuclear application technique was applied in this study by using radiotracer of 203Hg.  A simple kinetic model was then constructed to predict the bioaccumulation capability of   by catfish. The result of experiments were shown that the uptake rate of difference Hg2+ concentration were 79.90 to 101.22 ml.g-1.d-1. Strong correlation between uptake rates with increasing Hg2+concentration. In addition, the elimination rates were range 0.080 – 0.081 day-1. The biology half time (t1/2b of Hg2+ in whole body catfish were 8.50 – 8.63 days.  However, no clear correlation  between elimination rate with increasing concentration of Hg2+. The calculation of Bio Concentration Factor (BCF shown catfish have capability to accumulated Hg maximum 1242.69 time than its concentration in water

  14. 10.6μm激光对HgCdTe焦平面器件热应力的分析%Theoretical analysis of thermal-stress effect of HgCdTe infrared focal plane device induced by 10.6 μm laser

    Institute of Scientific and Technical Information of China (English)

    郝向南; 聂劲松; 李化; 卞进田; 雷鹏

    2012-01-01

    建立了HgCdTe红外焦平面器件的多膜层理论模型,利用有限元分析的方法,对10.6 μm激光辐照下HgCdTe红外焦平面器件的升温情况与热应力分布情况进行模拟,并通过参考已有文献的实验结果,验证了理论模型的合理性.理论分析结果表明:激光作用时探测器的温度场变化剧烈,200 W/cm2连续激光作用1 s后,HgCdTe感光层所受热应力为-986 MPa;脉宽100 ns,功率密度15 MW/cm2脉冲激光作用后,HgCdTe感光层所受热应力为-1300 MPa,都比器件制造过程中由于热失配而产生的热应力大;应力损伤发生的概率增大,可能比热损伤先发生,是HgCdTe红外焦平面器件激光损伤中的重要原因.%Muti-layer theoretical Model of HgCdTe Infrared Focal Plane Device was established. With the method of finite element analysis, temperature field and thermal-stress field induced by 10.6 μm laser were simulated. By considering experiments carried out in other papers as reference,the rationality and feasibility of the muti-layer model are proved. Results of theoretical analysis indicates that the temperature field changes greatly when irradiated by laser. With CW laser of 200 W/cm2 power density irradiating the sensor for 1 s, thermal-stress of HgCdTe photo-sensitive surface is -986MPa:With pulsed laser of 100 ns and 15 MW/cm2 irradiating the sensor,thermal-stress of HgCdTe photo-sensitive surface is - 1300 Mpa. The thermal-stress mentioned above are both beyond that caused by thermal-mismatch in the production process. Besides, the probability of thermal-stress damage increases and may happen before thermal damage,which should be an important factor in the research of laser damage to HgCdTe Infrared Focal Plane Device.

  15. Analysis of toxic trace elements in sea food samples by neutron activation

    International Nuclear Information System (INIS)

    The contents of toxic and essential trace element were analysed such as As, Hg, Se and Zn by neutron activation analysis in coastal fishes consumed by the general population of Malaysia. The mean values of the elements analysed expressed in mg/kg fresh weight ranged 1.42-5.61, 0.06-0.42, 4.2-20.6, 0.41-1.28 for As, Hg, Zn and Se, respectively. The maximum permissible limit for As in food was set at 1.0 mg/kg under the Malaysian Food Regulations. The results showed that consumption of coastal fishes is not permitted under the regulations, while the levels of Hg, Se and Zn were within the permissible limits. The daily dietary intake of As and Hg at 400 μg and 30 μg respectively are still within the tolerance levels. (author) 9 refs.; 2 tabs

  16. Relationships between hepatic trace element concentrations, reproductive status, and body condition of female greater scaup

    Science.gov (United States)

    Badzinski, S.S.; Flint, P.L.; Gorman, K.B.; Petrie, S.A.

    2009-01-01

    We collected female greater scaup (Aythya marila) on the Yukon-Kuskokwim Delta, Alaska during two breeding seasons to determine if concentrations of 18 trace elements in livers and eggs were elevated and if hepatic concentrations correlated with body condition or affected reproductive status. Fifty-six percent, 5%, and 42% of females, respectively, had elevated hepatic cadmium (Cd: >3 ??g g-1 dry weight [dw]), mercury (Hg: >3 ??g g-1 dw), and selenium (Se: >10 ??g g-1 dw). Somatic protein and lipid reserves were not correlated with hepatic Cd or Hg, but there was a weak negative correlation between protein and Se. Hepatic Cd, Hg, and Se were similar in females that had and had not initiated egg production. In a sample of six eggs, 33% and 100%, respectively, contained Se and Hg, but concentrations were below embryotoxicity thresholds. We conclude that trace element concentrations documented likely were not adversely impacting this study population. ?? 2009 Elsevier Ltd.

  17. Micromagnetic sensors and Dirac fermions in HgTe heterostructures

    Energy Technology Data Exchange (ETDEWEB)

    Buettner, Bastian

    2012-08-06

    Within the scope of this thesis two main topics have been investigated: the examination of micromagnetic sensors and transport of massive and massless Dirac fermions in HgTe quantum wells. For the investigation of localized, inhomogeneous magnetic fields, the fabrication and characterization of two different non-invasive and ultra sensitive sensors has been established at the chair ''Experimentelle Physik'' of the University of Wuerzburg. The first sensor is based on the young technique named micro-Hall magnetometry. The necessary semiconductor devices (Hall cross structures) were fabricated by high-resolution electron beam lithography based on two different two dimensional electron gases (2DEGs), namely InAs/(Al,Ga)Sb- and HgTe/(Hg,Cd)Te-heterostructures. The characteristics have been examined in two different ways. Measurements in homogeneous magnetic fields served for characterization of the sensors, whereas the investigation of artificially produced sub-{mu}m magnets substantiates the suitability of the devices for the study of novel nanoscale magnetic materials (e.g. nanowires). Systematic experiments with various magnets are in accordance with the theory of single-domain particles and anisotropic behavior due to shapes with high aspect ratio. The highest sensitivity for strongly localized fields was obtained at T=4.2 K for a (200.200) nm{sup 2} Hall cross - made from shallow, high mobility HgTe 2DEG. Although the field resolution was merely {delta}B{approx}100 {mu}T, the nanoscale sensor size yields an outstanding flux resolution of {delta}{Phi}=2.10{sup -3} {Phi}{sub 0}, where {Phi}{sub 0}=h/2e is the flux quantum. Translating this result in terms of magnetic moment, the sensitivity allows for the detection of magnetization changes of a particle centered on top of the sensor as low as {delta}M{approx}10{sup 2} {mu}{sub B}, with the magnetic moment of a single electron {mu}{sub B}, the Bohr magneton. The further examination of a permalloy

  18. CeO2-TiO2 catalysts for catalytic oxidation of elemental mercury in low-rank coal combustion flue gas.

    Science.gov (United States)

    Li, Hailong; Wu, Chang-Yu; Li, Ying; Zhang, Junying

    2011-09-01

    CeO(2)-TiO(2) (CeTi) catalysts synthesized by an ultrasound-assisted impregnation method were employed to oxidize elemental mercury (Hg(0)) in simulated low-rank (sub-bituminous and lignite) coal combustion flue gas. The CeTi catalysts with a CeO(2)/TiO(2) weight ratio of 1-2 exhibited high Hg(0) oxidation activity from 150 to 250 °C. The high concentrations of surface cerium and oxygen were responsible for their superior performance. Hg(0) oxidation over CeTi catalysts was proposed to follow the Langmuir-Hinshelwood mechanism whereby reactive species from adsorbed flue gas components react with adjacently adsorbed Hg(0). In the presence of O(2), a promotional effect of HCl, NO, and SO(2) on Hg(0) oxidation was observed. Without O(2), HCl and NO still promoted Hg(0) oxidation due to the surface oxygen, while SO(2) inhibited Hg(0) adsorption and subsequent oxidation. Water vapor also inhibited Hg(0) oxidation. HCl was the most effective flue gas component responsible for Hg(0) oxidation. However, the combination of SO(2) and NO without HCl also resulted in high Hg(0) oxidation efficiency. This superior oxidation capability is advantageous to Hg(0) oxidation in low-rank coal combustion flue gas with low HCl concentration. PMID:21770402

  19. Oxidation of elemental mercury in the atmosphere; Constraints imposed by global scale modelling

    Energy Technology Data Exchange (ETDEWEB)

    Bergan, Torbjoern; Rodhe, Henning [Stockholm Univ. (Sweden). Dept. of Meteorology

    2000-05-01

    Based on the global mercury model published by Bergan et al. (1999), we present here further results from simulations where the central theme has been to evaluate the role of ozone and the hydroxyl radical as possible gas phase oxidants for the oxidation of elemental mercury in the atmosphere. The magnitude of natural and man-made mercury emissions are taken from recent literature estimates and the flux from land areas is assumed to vary by season. We consider only two mercury reservoirs, elemental mercury, Hg{sup 0}, and the more soluble divalent form, Hgll. Wet and dry deposition of Hgll is explicitly treated. Applying monthly mean fields of ozone for the oxidation of gas phase Hg{sup 0} and using the reaction rate by Hall (1995) yields a global transformation of Hg{sup 0} to Hgll which is too slow to keep the simulated concentration of Hg{sup 0} near observed values. This shows that there are additional important removal processes for Hg{sup 0} or that the reaction rate proposed by Hall (1995) is too slow. A simulation in which the oxidation rate was artificially increased, so that the global turn-over time of Hg{sup 0} was one year and the simulated average concentration of Hg{sup 0} was realistic, produced latitudinal and seasonal variations in Hg{sup 0} that did not support the hypothesis that gas phase reaction with O{sub 3} is the major oxidation process for Hg{sup 0}. Recent studies indicate that OH may be an important gas phase oxidant for Hg{sup 0}. Using OH as the oxidant and applying the preliminary oxidation rate by Sommar et al. (1999) gave an unrealistically large removal of Hg{sup 0} from the atmosphere. From calculations using a slower reaction rate, corresponding to a turn-over time of Hg{sup 0} of one year, we calculated concentrations of both Hg{sup 0} in surface air and Hgll in precipitation which correspond, both in magnitude and temporal variation, to seasonal observations in Europe and North America. This result supports the suggestion that

  20. A review of trace element emissions from the combustion of refuse-derived fuel with coal

    International Nuclear Information System (INIS)

    The effects of cocombusting refuse-derived fuel (RDF) with coal on stack emissions of trace elements in the ash stream were reviewed. The large number of variables and uncertainties involved precluded drawing definitive conclusions regarding many of the trace elements. However, it is evident that cocombustion resulted in increased emissions of Cd, Cu, Hg, Pb, and Zn. Emissions of As and Ni tended to decrease when RDF was fired with coal. Modeling studies indicated that ambient levels of trace elements during cocombustion should be within acceptable limits. However, periodic monitoring of Cd, Hg, and Pb may be warranted in some instances

  1. Dynamic recycling of gaseous elemental mercury in the boundary layer of the Antarctic Plateau

    Directory of Open Access Journals (Sweden)

    A. Dommergue

    2012-11-01

    Full Text Available Gaseous elemental mercury (Hg0 was investigated in the troposphere and in the interstitial air extracted from the snow at Dome Concordia station (alt. 3320 m on the Antarctic Plateau during January 2009. Measurements and modeling studies showed evidence of a very dynamic and daily cycling of Hg0 inside the mixing layer with a range of values from 0.2 ng m−3 up to 2.3 ng m−3. During low solar irradiation periods, fast Hg0 oxidation processes in a confined layer were suspected. Unexpectedly high Hg0 concentrations for such a remote place were measured under higher solar irradiation due to snow photochemistry. We suggest that a daily cycling of reemission/oxidation occurs during summer within the mixing layer at Dome Concordia. Hg0 concentrations showed a negative correlation with ozone mixing ratios, which contrasts with atmospheric mercury depletion events observed during the Arctic spring. Unlike previous Antarctic studies, we think that atmospheric Hg0 removal may not be the result of advection processes. The daily and dramatic Hg0 losses could be a consequence of surface or snow induced oxidation pathways. It remains however unclear whether halogens are involved. The cycling of other oxidants should be investigated together with Hg species in order to clarify the complex reactivity on the Antarctic plateau.

  2. Removal of elemental mercury by iodine-modified rice husk ash sorbents

    Institute of Scientific and Technical Information of China (English)

    Pengfei Zhao; Xin Guo; Chuguang Zheng

    2010-01-01

    Iodine-modified calcium-based rice husk ash sorbents (I2/CaO/RHA) were synthesized and characterized by X-ray diffraction,X-ray fluorescence,and N2 isotherm adsorpdon/desorption.Adsorption experiments of vapor-phase elemental mercury (Hg0) were performed in a laboratory-scale fixed-bed reactor.I2/CaO/RHA performances on Hg0 adsorption were compared with those of modified Cabased fly ash sorbents (I2/CaO/FA) and modified fly ash sorbents (I2/FA).Effects of oxidant loading,supports,pore size distribution,iodine impregnation modes,and temperature were investigated as well to understand the mechanism in capturing Hg0.The modified sorbents exhibited reasonable efficiency for Hg0 removal under simulated flue gas.The surface area,pore size distribution,and iodine impregnation modes of the sorbents did not produce a strong effect on Hg0 capture efficiency,while fair correlation was observed between Hg0 uptake capacity and iodine concentration.Therefore,the content of I2 impregnated on the sorbents was identified as the most important factor influencing the capacity of these sorbents for Hg0 uptake.Increasing temperature in the range of 80-140℃ caused a rise in Hg0 removal.A reaction mechanism that may explain the experimental results was presumed based on the characterizations and adsorption study.

  3. Shape coexistence in neutron-deficient Hg isotopes studied via lifetime measurements in $^{184,186}$Hg and two-state mixing calculations

    CERN Document Server

    Gaffney, L P; Page, R.D.; Grahn, T.; Scheck, M.; Butler, P.A.; Bertone, P.F.; Bree, N.; Carroll, R.J.; Carpenter, M.P.; Chiara, C.J.; Dewald, A.; Filmer, F.; Fransen, C.; Huyse, M.; Janssens, R.V.F.; Joss, D.T.; Julin, R.; Kondev, F.G.; Nieminen, P.; Pakarinen, J.; Rigby, S.V.; Rother, W.; Van Duppen, P.; Watkins, H.V.; Wrzosek-Lipska, K.; Zhu, S.

    2014-01-01

    The neutron-deficient mercury isotopes, $^{184,186}$Hg, were studied with the Recoil Distance Doppler Shift (RDDS) method using the Gammasphere array and the K\\"oln Plunger device. The Differential Decay Curve Method (DDCM) was employed to determine the lifetimes of the yrast states in $^{184,186}$Hg. An improvement on previously measured values of yrast states up to $8^{+}$ is presented as well as first values for the $9_{3}$ state in $^{184}$Hg and $10^{+}$ state in $^{186}$Hg. $B(E2)$ values are calculated and compared to a two-state mixing model which utilizes the variable moment of inertia (VMI) model, allowing for extraction of spin-dependent mixing strengths and amplitudes.

  4. Radionuclides for investigating the accumulation of toxic elements in algae and fish

    International Nuclear Information System (INIS)

    Radionuclides are very suitable for investigating the accumulation of toxic elements in algae and fish. The most important results obtained from using 51Cr(III) (VI), 65Zn, 74As(III) (V), CH374AsO(OH)2, (CH3)274AsO(OH), (CH3)374As, 85Sr, 86Rb, /sup 115m/Cd, 133Ba, 137Cs, 203Hg(II), CH3203HgCl and C6H5203HgCl for the study of the accumulation, release and chemical transformation of the above species in algae and fish are summarized. (author)

  5. HgTe and CdTe epitaxial layers and HgTe–CdTe superlattices grown by laser molecular beam epitaxy

    OpenAIRE

    Cheung, J. T.; Niizawa, G.; Moyle, J.; Ong, N. P.; Paine, B. M.; Vreeland, T., Jr.

    1986-01-01

    CdTe and HgTe epilayers and HgTe/CdTe superlattices have been grown by laser molecular beam epitaxy (laser MBE) on CdTe substrates. The power density of the laser radiation used to evaporate source materials was found to be a very important growth parameter. The superlattice structures have been characterized by helium ion backscattering spectrometry, x-ray double crystal diffractometry, and low temperature electrical transport measurements. Results indicate good crystallinity and very strong...

  6. Investigation of magnetoabsorption at different temperatures in HgTe/CdHgTe quantum-well heterostructures in pulsed magnetic fields

    Energy Technology Data Exchange (ETDEWEB)

    Platonov, V. V.; Kudasov, Yu. B.; Makarov, I. V.; Maslov, D. A.; Surdin, O. M. [Sarov Physical–Technical Institute—National Research Nuclear University MEPhI (Russian Federation); Zholudev, M. S.; Ikonnikov, A. V.; Gavrilenko, V. I. [Russian Academy of Sciences, Institute of Physics of Microstructures (Russian Federation); Mikhailov, N. N.; Dvoretsky, S. A. [Russian Academy of Sciences, Rzhanov Institute of Semiconductor Physics, Siberian Branch (Russian Federation)

    2015-12-15

    The magnetoabsorption in magnetic fields as high as 40 T is investigated at T > 77 K in HgTe/CdHgTe quantum-well heterostructures (d{sub QW} ≈ 8 nm). The spectra reveal two lines associated both with intraband transition from the lower Landau level in the conduction band and with interband transition. It is shown that the band structure in these systems changes from inverted to normal with increasing temperature.

  7. Viscosity Relaxation in Molten HgZnTe

    Science.gov (United States)

    Baird, James K.

    2002-01-01

    Because of its narrow electronic band-gap, HgZnTe solid solutions have been proposed as effective detectors for infrared radiation. To produce the best single crystals of these materials for this application, knowledge of the phase diagram that governs the freezing of the liquid is essential. Besides the phase diagram, however, some information concerning the thermophysical properties of the melt, such as viscosity, density, specific heat, and enthalpy of mixing, can also be useful. Of these thermophysical properties, the viscosity is perhaps of the most interest scientifically. Measurements using the oscillating cup method have shown that the isothermal melt requires tens of hours of equilibration time before a steady value of the viscosity can be achieved. Over this equilibration time, which depends upon temperature, the viscosity can increase by as much as a factor of two before reaching a steady state. We suggest that this relaxation phenomenon may be due to a slight polymerization of Te atoms in the melt. To account for the time dependence of the viscosity in the HgZnTe melt, we propose that the liquid acts as a solvent that favors the formation of Te atom chains. We suggest that as the melt is cooled from a high temperature to the temperature for measurement of the viscosity, a free radical polymerization of Te atoms begins. To estimate this average molecular weight, we use a simple free radical polymerization mechanism, including a depolymerization step, to calculate the time dependence to the concentration of each Te polymer molecular weight fraction. From these molecular weight fractions, we compute the weight average molecular weight of the distribution. Using the semi-empirical relation between average molecular weight and viscosity, we obtain a formula for the time dependence of the viscosity of the melt. Upon examining this formula, we find that the viscosity achieves a steady value when a balance is achieved between the rate of formation of the chains

  8. Sensitivity analysis of an updated bidirectional air–surface exchange model for elemental mercury vapor

    OpenAIRE

    Wang, X.; Lin, C.-J.; Feng, X.

    2014-01-01

    A box model for estimating bidirectional air–surface exchange of gaseous elemental mercury (Hg0) has been updated based on the latest understanding of the resistance scheme of atmosphere–biosphere interface transfer. Simulations were performed for two seasonal months to evaluate diurnal and seasonal variation. The base-case results show that water and soil surfaces are net sources, while vegetation is a net sink of Hg0. The estimated net exchange in a domain covering the con...

  9. Elevated blood Hg at recommended seafood consumption rates in adult seafood consumers.

    Science.gov (United States)

    Karimi, Roxanne; Silbernagel, Susan; Fisher, Nicholas S; Meliker, Jaymie R

    2014-09-01

    Mercury (Hg) exposure from seafood continues to be a public health concern due to health effects from elevated exposure, increasing worldwide seafood consumption, and continued Hg inputs into the environment. Elevated Hg exposure can occur in populations with specialized diets of sport-caught freshwater fish. However, we need a better understanding of Hg exposure from seafood, the most common exposure source, and from specific seafood types. We examined Hg exposure in avid seafood consumers, and the seafood items and consumption frequency that confer the largest Hg exposure. Adult, avid seafood consumers, in Long Island, NY, USA, with blood total Hg concentrations predicted to exceed the USEPA reference concentration that is considered safe (5.8 μg L(-1)), were eligible for the study; 75% of self-reported avid seafood consumers were eligible to participate. We measured blood total Hg concentrations and seafood consumption in 285 participants. We examined relationships between Hg and seafood consumption using multiple linear regression. Seafood consumption rate for our population (14.4 kg yr(-1)) was >2 times that estimated for the U.S. (6.8 kg yr(-1)), and lower than the worldwide estimate (18.4 kg yr(-1)). Mean blood Hg concentration was 4.4 times the national average, and 42% of participants had Hg concentrations exceeding 5.8 μg L(-1). Elevated Hg exposures occurred at all seafood consumption frequencies, including the recommended frequency of 2 meals per week. Blood Hg concentrations were positively associated with weekly tuna steak or sushi intake (β=6.30 change in blood Hg, μg L(-1)) and monthly (β=2.54) or weekly (β=9.47) swordfish, shark or marlin intake. Our findings show that seafood consumers in this population have elevated Hg exposures even at relatively low seafood consumption rates that are at or below current dietary recommendations. Further study should examine health risks and benefits of avid seafood consumption, and consider modifying

  10. Microsolvation of methylmercury: structures, energies, bonding and NMR constants ((199)Hg, (13)C and (17)O).

    Science.gov (United States)

    Flórez, Edison; Maldonado, Alejandro F; Aucar, Gustavo A; David, Jorge; Restrepo, Albeiro

    2016-01-21

    Hartree-Fock (HF) and second order perturbation theory (MP2) calculations within the scalar and full relativistic frames were carried out in order to determine the equilibrium geometries and interaction energies between cationic methylmercury (CH3Hg(+)) and up to three water molecules. A total of nine structures were obtained. Bonding properties were analyzed using the Quantum Theory of Atoms In Molecules (QTAIM). The analyses of the topology of electron densities reveal that all structures exhibit a partially covalent HgO interaction between methylmercury and one water molecule. Consideration of additional water molecules suggests that they solvate the (CH3HgOH2)(+) unit. Nuclear magnetic shielding constants σ((199)Hg), σ((13)C) and σ((17)O), as well as indirect spin-spin coupling constants J((199)Hg-(13)C), J((199)Hg-(17)O) and J((13)C-(17)O), were calculated for each one of the geometries. Thermodynamic stability and the values of NMR constants correlate with the ability of the system to directly coordinate oxygen atoms of water molecules to the mercury atom in methylmercury and with the formation of hydrogen bonds among solvating water molecules. Relativistic effects account for 11% on σ((13)C) and 14% on σ((17)O), which is due to the presence of Hg (heavy atom on light atom, HALA effect), while the relativistic effects on σ((199)Hg) are close to 50% (heavy atom on heavy atom itself, HAHA effect). J-coupling constants are highly influenced by relativity when mercury is involved as in J((199)Hg-(13)C) and J((199)Hg-(17)O). On the other hand, our results show that the values of NMR constants for carbon and oxygen, atoms which are connected through mercury (C-HgO), are highly correlated and are greatly influenced by the presence of water molecules. Water molecules introduce additional electronic effects to the relativistic effects due to the mercury atom. PMID:26670708

  11. Microsolvation of methylmercury: structures, energies, bonding and NMR constants ((199)Hg, (13)C and (17)O).

    Science.gov (United States)

    Flórez, Edison; Maldonado, Alejandro F; Aucar, Gustavo A; David, Jorge; Restrepo, Albeiro

    2016-01-21

    Hartree-Fock (HF) and second order perturbation theory (MP2) calculations within the scalar and full relativistic frames were carried out in order to determine the equilibrium geometries and interaction energies between cationic methylmercury (CH3Hg(+)) and up to three water molecules. A total of nine structures were obtained. Bonding properties were analyzed using the Quantum Theory of Atoms In Molecules (QTAIM). The analyses of the topology of electron densities reveal that all structures exhibit a partially covalent HgO interaction between methylmercury and one water molecule. Consideration of additional water molecules suggests that they solvate the (CH3HgOH2)(+) unit. Nuclear magnetic shielding constants σ((199)Hg), σ((13)C) and σ((17)O), as well as indirect spin-spin coupling constants J((199)Hg-(13)C), J((199)Hg-(17)O) and J((13)C-(17)O), were calculated for each one of the geometries. Thermodynamic stability and the values of NMR constants correlate with the ability of the system to directly coordinate oxygen atoms of water molecules to the mercury atom in methylmercury and with the formation of hydrogen bonds among solvating water molecules. Relativistic effects account for 11% on σ((13)C) and 14% on σ((17)O), which is due to the presence of Hg (heavy atom on light atom, HALA effect), while the relativistic effects on σ((199)Hg) are close to 50% (heavy atom on heavy atom itself, HAHA effect). J-coupling constants are highly influenced by relativity when mercury is involved as in J((199)Hg-(13)C) and J((199)Hg-(17)O). On the other hand, our results show that the values of NMR constants for carbon and oxygen, atoms which are connected through mercury (C-HgO), are highly correlated and are greatly influenced by the presence of water molecules. Water molecules introduce additional electronic effects to the relativistic effects due to the mercury atom.

  12. Coulomb excitation of $^{182-184}$ Hg: Shape coexistence in the neutron-deficient lead region

    CERN Multimedia

    We put forward a study of the interplay between individual nucleon behavior and collective degrees of freedom in the nucleus, as manifested in shape coexistence in the neutron-deficient lead region. As a first step of this experimental campaign, we propose to perform Coulomb excitation on light mercury isotopes to probe their excited states and determine transitional and diagonal E2 matrix elements, especially reducing the current uncertainties. The results from previous Coulomb excitation measurements in this mass region performed with 2.85 MeV/u beams from REX-ISOLDE have shown the feasibility of these experiments. Based on our past experience and the results obtained, we propose a detailed study of the $^{182-184}$Hg nuclei, that exhibit a pronounced mixing between 2 low-lying excited states of apparently different deformation character, using the higher energy beams from HIE-ISOLDE which are crucial to reach our goal. The higher beam energy should result in an increased sensitivity with respect to the qua...

  13. A nearby GRB host galaxy: VLT/X-shooter observations of HG 031203

    CERN Document Server

    Guseva, N G; Fricke, K J; Henkel, C; 10.1051/0004-6361/201116765

    2011-01-01

    (abridged) Long-duration gamma-ray bursts (LGRBs) occur in galaxies of generally low metallicity. We aim at a spectroscopic analysis of HG 031203, the host galaxy of a LRGB burst, to obtain its properties. Based on VLT/X-shooter spectroscopic observations in the wavelength range 3200-24000A, we use standard direct methods to evaluate physical conditions and element abundances. The resolving power of the instrument also allowed us to trace the kinematics of the ionised gas. We derive an interstellar oxygen abundance of 12+logO/H=8.20+/-0.03. The observed fluxes of hydrogen lines correspond to the theoretical recombination values after correction for extinction with a single value C(Hbeta)=1.67. We produce the CLOUDY photoionisation HII region model that reproduces observed emission-line fluxes of different ions in the optical range. This model also predicts emission-line fluxes in the near-infrared (NIR) and mid-infrared (MIR) ranges that agree well with the observed ones. This implies that the star-forming re...

  14. Particulate contacts to Si and CdTe: Al, Ag, Hg-Cu-Te, and Sb-Te

    Science.gov (United States)

    Schulz, Douglas L.; Ribelin, Rosine; Curtis, Calvin J.; Ginley, David S.

    1999-03-01

    Our team has been investigating the use of particle-based contacts in both Si and CdTe solar cell technologies. First, in the area of contacts to Si, powders of Al and Ag prepared by an electroexplosion process have been characterized by transmission electron microscopy (TEM), TEM elemental determination X-ray spectroscopy (TEM-EDS), and TEM electron diffraction (TEM-ED). These Al and Ag particles were slurried and tested as contacts to p- and n-type silicon wafers, respectively. Linear current-voltage (I-V) was observed for Ag on n-type Si, indicative of an ohmic contact, whereas the Al on p-type Si sample was non-ideal. A wet-chemical surface treatment was performed on one Al sample and TEM-EDS indicated a substantial decrease in the O contaminant level. The treated Al on p-type Si films exhibited linear I-V after annealing. Second, in the area of contacts to CdTe, particles of Hg-Cu-Te and Sb-Te have been applied as contacts to CdTe/CdS/SnO2 heterostructures prepared by the standard NREL protocol. First, Hg-Cu-Te and Sb-Te were prepared by a metathesis reaction. After CdCl2 treatment and NP etch of the CdTe layer, particle contacts were applied. The Hg-Cu-Te contacted cells exhibited good electrical characteristics, with Voc>810 mV and efficiencies > 11.5% for most cells. Although Voc>800 mV were observed for the Sb-Te contacted cells, efficiencies in these devices were limited to 9.1% presumably by a large series resistance (>20 Ω) observed in all samples.

  15. Can graphene make better HgCdTe infrared detectors?

    Directory of Open Access Journals (Sweden)

    Shi Yanli

    2011-01-01

    Full Text Available Abstract We develop a simple and low-cost technique based on chemical vapor deposition from which large-size graphene films with 5-10 graphene layers can be produced reliably and the graphene films can be transferred easily onto HgCdTe (MCT thin wafers at room temperature. The proposed technique does not cause any thermal and mechanical damages to the MCT wafers. It is found that the averaged light transmittance of the graphene film on MCT thin wafer is about 80% in the mid-infrared bandwidth at room temperature and 77 K. Moreover, we find that the electrical conductance of the graphene film on the MCT substrate is about 25 times larger than that of the MCT substrate at room temperature and 77 K. These experimental findings suggest that, from a physics point of view, graphene can be utilized as transparent electrodes as a replacement for metal electrodes while producing better and cheaper MCT infrared detectors.

  16. ROIC for HgCdTe e-APD FPA

    Science.gov (United States)

    Chen, Guoqiang; Zhang, Junling; Wang, Pan; Zhou, Jie; Gao, Lei; Ding, Ruijun

    2013-08-01

    Ultra-low light imaging and passive/active dual mode imaging require very low noise optical receivers to achieve detection of fast and weak optical signal. HgCdTe electrons initiated avalanche photodiodes (e-APDs) in linear multiplication mode is the detector of choice thanks to its high quantum efficiency, high gain at low bias, high bandwidth and low noise factor. In my work, a passive/active dual mode readout integrated circuit (ROIC) of e-APD focal plane array (FPA) is designed. Unit cell circuit architecture of ROIC includes a capacitance feedback transimpedance amplifier (CTIA) as preamplifier of ROIC, a high voltage protection module, a comparator, a Sample-Hold circuit module, and output driver stage. There is a protection module in every unit cell circuit which can avoid ROIC to be damaged from avalanche breakdown of some diodes of detector. Conventional 5V CMOS process is applied to implement the high voltage protection with the small area rather than Laterally Diffused Metal Oxide Semiconductor (LDMOS) in high voltage BCD process in the limited 100um×100um pitch area. In CTIA module, three integration capacitances are included in the CTIA module, two of them are switchable to provide different well capacity and noise. Constraints such as pixel area, stability and power lead us design toward a simple one-stage cascade operational transconductance amplifier (OTA) as pre-amplifier. High voltage protection module can protect ROIC to be damaged because of breakdown of some avalanche diodes.

  17. Radiographic element

    International Nuclear Information System (INIS)

    Radiographic elements are disclosed comprised of first and second silver halide emulsion layers separated by an interposed support capable of transmitting radiation to which the second image portion is responsive. At least the first imaging portion contains a silver halide emulsion in which thin tubular silver halide grains of intermediate aspect ratios (from 5:1 to 8:1) are present. Spectral sensitizing dye is adsorbed to the surface of the tubular grains. Increased photographic speeds can be realized at comparable levels of crossover. (author)

  18. Elemental composition of human and animal milk

    International Nuclear Information System (INIS)

    A review is presented of the elemental composition of human and animal milk with special reference to trace elements determined through nuclear techniques, particularly neutron activation analysis (NAA). In the joint IAEA/WHO research project, 16 of the 24 elements under investigation have been analysed by NAA with the aid of advanced research nuclear reactors. Literature data are discussed and tabulated in 50 separate tables (one for each element) mainly for the period after 1950. Each table uses a standard format comprising 10 columns indicating (1) source of milk (e.g. human or animal), (2) status of the milk (colostrum, transitional or mature), (3) country of origin, (4) year of data publication, (5) mean concentration, (6) range of single values or standard deviation of the mean, (7) number of samples analysed, (8) analytical technique employed, (9) literature source of the data, and (10) relevant remarks, if any. The most abundant data refer to the minor elements Ca, Cl, K, Mg, N, Na, P and S and to the trace elements Cu, Fe and Zn. Fewer data are available for Cd, Hg, I, Mn, Pb and Se. For the remaining elements, including such biologically important trace elements as As, Co, Cr, F, Mo, Ni, Si and Sn, very few reliable data so far appear to exist

  19. Toxic metal dispersion in mining areas: from point source to diffusion pollution. The case of the Mt. Amiata Hg mining district (Southern Tuscany - Italy): new results.

    Science.gov (United States)

    Colica, Antonella; Chiarantini, Laura; Rimondi, Valentina; Benvenuti, Marco; Costagliola, Pilario; Lattanzi, Pierfranco; Paolieri, Mario; Rinaldi, Massimo

    2016-04-01

    Rivers draining mining areas may contribute to the diffusion of contaminants through their dispersion and accumulation into different morphological river units. The Paglia River's catchment (southern Tuscany) hosts the SE portion of the Mt. Amiata mercury district, the third most important worldwide (exploited from 1880 to 1980 with a total production of 100,000 tonnes Hg) before becoming a tributary of the Tiber River, which directly flows into Mediterranean Sea. The goals of this study are: 1) to recognize and distinguish different morphological units along the Paglia River watercourse, 2) to determine spatial/temporal distribution and concentration of Hg (and other toxic elements, particularly As) in different units. The analysis of morphological units was made by mapping their evolution from the beginning of mining activity (1883) to present day along 43 km of the Paglia watercourse defining eleven morphological sections across this river, and one across one of its tributaries, the Siele Creek, which drains various Hg mines located upstream. Four fundamental morphological/sedimentary unit types have been distinguished: stream sediments, bar, floodplain, and terraces. The latter occur in various orders and age: Pleistocenic, pre-mining (i.e., dating before 1880), and coeval to the mining activity. A total of 100 samples were taken from the various units in the selected transects, georeferenced and then analyzed for their Hg and As contents by ICP-OES. Arsenic contents generally never exceed 10 mg/kg. The observed ranges are: stream sediments 4.1÷8.2 mg/kg; bars 4.1÷6.6 mg/kg; floodplains 3.8÷6.6 mg/kg; terrace coeval with mining activity 3.2÷10.1 mg/kg. Hg contents in present-day stream sediments and bars are extremely variable (0.2÷27.5 and 1.4÷22.4 mg/kg respectively), and show a sharp increase at the confluence with Siele Creek. Floodplain sediments may reach up to 98 mg/kg. Terraces coeval with mining activity also show variable Hg contents (0.1÷66

  20. Physical properties and band structure of crystals (3HgTe1–x(Al2Te3x, doped with manganese

    Directory of Open Access Journals (Sweden)

    Maryanchuk P. D.

    2014-06-01

    Full Text Available This paper presents the results of the analysis of magnetic, optical, kinetic properties and band parameters of (3HgTe1–x(Al2Te3x crystals doped by manganese. The behavior of the magnetic susceptibility of the (3HgTe1–x(Al2Te3x: crystals can be explained by the presence of Mn—Тe—Mn—Тe clusters or, more precisely, by their transition from a magnetically ordered to a paramagnetic state at Curie temperature Tc. The temperature dependences of electrical conductivity are typical for semiconductor materials. This is due to the increase in carrier concentration with the increase of temperature. The temperature dependence of the Hall coefficient indicates that electrons and holes participate in the transport phenomena in the studied samples (the conductivity is mixed. In (3HgTe1–x(Al2Te3x: crystals, the electron mobility decreases with increasing temperature, indicating the predominance of the scattering of the charge carriers on thermal vibrations of the crystal lattice. Thermoelectric power for the samples under investigation possesses negative values and increases in absolute value with the rise of temperature. The optical band gap of the samples was defined from the optical studies. We have measured current-voltage characteristics of n-TiO2/(3HgTe1–x(Al2Te3x: and n-TiN/(3HgTe1–x(Al2Te3x: heterojunctions at room temperature. The band gap, the matrix element of the interband interaction and the electron effective mass at the bottom of the conduction band were determined from the concentration dependence of the electrons effective mass at the Fermi level.

  1. Modification and characterization of PET fibers for fast removal of Hg(II), Cu(II) and Co(II) metal ions from aqueous solutions

    Energy Technology Data Exchange (ETDEWEB)

    Monier, M., E-mail: monierchem@yahoo.com [Chemistry Department, Faculty of Science, Mansoura University, Mansoura (Egypt); Abdel-Latif, D.A. [Chemistry Department, Faculty of Science, Mansoura University, Mansoura (Egypt)

    2013-04-15

    Highlights: ► PET fibers were graft copolymerized with acrylonitrile. ► Further modification was carried out through the reaction with hydrazine hydrate and then potassium thiocyanate. ► The resulted chelating fibers were characterized by various instrumental methods. ► The fibers were applied to remove Hg{sup 2+}, Cu{sup 2+} and Co{sup 2+} from aqueous solutions. -- Abstract: A new chelating fiber (PET-TSC) was prepared with PET for fast removal of Hg{sup 2+}, Cu{sup 2+} and Co{sup 2+} from water. Elemental analysis, SEM, BET surface area, {sup 13}C NMR, FTIR and X-ray diffraction spectra were used to characterize PET-TSC. The higher uptake capacity of the studied metal ions was observed at higher pH values. Kinetic study indicated that the adsorption of Hg{sup 2+}, Cu{sup 2+} and Co{sup 2+} followed the pseudo-second-order equation, suggesting chemical sorption as the rate-limiting step of the adsorption process. The best interpretation for the equilibrium data was given by Langmuir isotherm, and the maximum adsorption capacities were 120.02, 96.81 and 78.08 mg/g for Hg{sup 2+}, Cu{sup 2+} and Co{sup 2+} ions, respectively. 1 M HCl or 0.1 M EDTA could be used as effective eluant to desorb the Hg{sup 2+}, Cu{sup 2+} and Co{sup 2+} adsorbed by PET-TSC, and the adsorption capacity of PET-TSC for the three heavy metal ions could still be maintained at about 90% level at the 5th cycle. Accordingly, it is expected that PET-TSC could be used as a promising adsorbent for fast removal of heavy metal ions from water, and the present work also might provide a simple and effective method to reuse the waste PET fibers.

  2. Potential of Brass to Remove Inorganic Hg(II) from Aqueous Solution through Amalgamation.

    Science.gov (United States)

    Wenke, Axel; Bollen, Anne; Richard, Jan-Helge; Biester, Harald

    2016-06-01

    Brass shavings (CuZn45) were tested for their efficiency to remove Hg(II) from contaminated groundwater through amalgamation. The study was focused on long-term retention efficiency, the understanding of the amalgamation process and kinetics, and influences of filter surface alteration. Column tests were performed with brass filters (thickness 3 to 9 cm) flushed with 1000 μg/L Hg solution for 8 hours under different flow rates (300 to 600 mL/h). Brass filters consistently removed >98% of Hg from solution independent of filter thickness and flow rate. In a long-term experiment (filter thickness 2 cm), Hg retention decreased from 96 to 92% within 2000 hours. Batch and column experiments for studying kinetics of Hg removal indicate ~100% Hg removal from solution within only 2 hours. Solid-phase mercury thermo-desorption analysis revealed that Hg(0) diffusion into the brass surface controls kinetics of mercury retention. Brass surface alteration could be observed, but did not influence Hg retention. PMID:27225782

  3. A measurement of the neutron to 199Hg magnetic moment ratio

    Directory of Open Access Journals (Sweden)

    S. Afach

    2014-12-01

    Full Text Available The neutron gyromagnetic ratio has been measured relative to that of the 199Hg atom with an uncertainty of 0.8 ppm. We employed an apparatus where ultracold neutrons and mercury atoms are stored in the same volume and report the result γn/γHg=3.8424574(30.

  4. Influence of Ga and Hg on microstructure and electrochemical corrosion behavior of Mg alloy anode materials

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    The effects of Hg and Ga on the electrochemical corrosion behavior of Mg-5%Hg (molar fraction) alloys were investigated by the measurement of polarization curves and galvanostatic test. The microstructure of the alloys and the corroded surface of the specimens were investigated by scanning electron microscopy, X-ray diffractometry and emission spectrum analysis. It can be concluded that the addition of 1%Ga (molar fraction) reduces corrosion current density from 26.98 mA/cm2 to 2.34 mA/cm2;while the addition of 1%Hg (molar fraction) increases corrosion current density. The addition of Ga and Hg both promotes the electrochemical activity of the alloys and the influence of Ga is more effective than Hg. Mg-5%Hg-1%Ga alloy has the best electrochemical activity, showing mean potential of-1.992 V. The activation mechanism of the magnesium alloy produced by Hg and Ga was put forward. Magnesium atoms are dissolved in liquid Hg and Ga to form amalgam and undergo severe oxidation at the amalgam/electrolyte interface.

  5. 40 CFR 75.83 - Calculation of Hg mass emissions and heat input rate.

    Science.gov (United States)

    2010-07-01

    ... heat input rate. 75.83 Section 75.83 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... Calculation of Hg mass emissions and heat input rate. The owner or operator shall calculate Hg mass emissions and heat input rate in accordance with the procedures in sections 9.1 through 9.3 of appendix F...

  6. Electrodeposited CdTe and HgCdTe solar cells

    Energy Technology Data Exchange (ETDEWEB)

    Basol, B.M.

    1988-01-15

    The processing steps necessary for producing high efficiency electrodeposited CdTe and HgCdTe solar cells are described. The key step in obtaining solar cell grade p-type CdTe and HgCdTe is the 'type conversion-junction formation' (TCJF) process. The TCJF process involves the heat treatment of the as-deposited n-type CdTe and HgCdTe layers at around 400 /sup 0/C. This procedure converts these n-type films into high resistivity p type and forms a rectifying junction between them and the underlying n-type window layers. Possible effects of oxygen on the TCJF process are discussed. The results of studies made on the structural, electrical and optical properties of the electrodeposited CdS, CdTe and HgCdTe films are presented. The resistivity of the electrodeposited HgCdTe can be made lower than that of CdTe. Consequently, solar cells made using the HgCdTe films have, on the average, better fill factors than those made using the CdTe layers, HgCdTe is also attractive for tandem-cell applications because of its variable band gap which can be easily tuned to the desired value. CdS/CdTe and CdS/HgCdTe heterojunction solar cells with 10.3% and 10.6% efficiency have been demonstrated using electrodeposition techniques and the TCJF process.

  7. Cleavable Molecular Beacon for Hg(2+) Detection Based on Phosphorothioate RNA Modifications.

    Science.gov (United States)

    Huang, Po-Jung Jimmy; Wang, Feng; Liu, Juewen

    2015-07-01

    Mercury is a highly toxic heavy metal, and detection of Hg(2+) by biosensors has attracted extensive research interest in the past decade. In particular, a number of DNA-based sensing strategies have been developed. Well-known examples include thymine-Hg(2+) interactions and Hg(2+)-activated DNAzymes. However, these mechanisms are highly dependent on buffer conditions or require hybridization with another DNA strand. Herein, we report a new mechanism based on Hg(2+)-induced cleavage of phosphorothioate (PS) modified RNA. Among the various metal ions tested, Hg(2+) induced the most significant cleavage (∼16%), while other metals cleaved less than 2% of the same substrate. The uncleaved substrate undergoes desulfurization in the presence of Hg(2+). This cleavage reaction yields a similar amount of product from pH 3.5 to 7 and in the temperature range between 20 and 90 °C. Various PS RNA junctions can be cleaved with a similar efficiency, but PS DNA junctions cannot be cleaved. A molecular beacon containing three PS RNA modifications is designed, detecting Hg(2+) down to 1.7 nM with excellent selectivity. This sensor can also detect Hg(2+) in the Lake Ontario water sample, although its response is significantly masked by fish tissues. PMID:26060876

  8. Self-consistent electronic-hand-structure calculation for Hg3AsF6

    NARCIS (Netherlands)

    Groot, R.A. de; Buiting, J.J.M.; Weger, M.; Mueller, F.M.

    1985-01-01

    The electronic structure of commensurate Hg3AsF6 is calculated using the self-consistent relativistic augmented-spherical-wave method. The results are compared with earlier pseudopotential calculations. The beat pattern as observed in the de Haas–van Alphen spectrum of Hg3–δAsF6 is interpreted as ar

  9. Progress in MOCVD growth of HgCdTe epilayers for HOT infrared detectors

    Science.gov (United States)

    Kebłowski, A.; Gawron, W.; Martyniuk, P.; Stepień, D.; Kolwas, K.; Piotrowski, J.; Madejczyk, P.; Kopytko, M.; Piotrowski, A.; Rogalski, A.

    2016-05-01

    In this paper we present progress in MOCVD growth of (100) HgCdTe epilayers achieved recently at the Institute of Applied Physics, Military University of Technology and Vigo System S.A. It is shown that MOCVD technology is an excellent tool in fabrication of different HgCdTe detector structures with a wide range of composition, donor/acceptor doping and without post grown annealing. Particular progress has been achieved in the growth of (100) HgCdTe epilayers for long wavelength infrared photoconductors operated in HOT conditions. The (100) HgCdTe photoconductor optimized for 13-μm attain detectivity equal to 6.5x109 Jones and therefore outperform its (111) counterpart. The paper also presents technological progress in fabrication of MOCVD-grown (111) HgCdTe barrier detectors. The barrier device performance is comparable with state-of-the-art of HgCdTe photodiodes. The detectivity of HgCdTe detectors is close to the value marked HgCdTe photodiodes. Dark current densities are close to the values given by "Rule 07".

  10. Mercury (Hg) in meteorites: variations in abundance, thermal release profile, mass-dependent and mass-independent isotopic fractionation

    CERN Document Server

    Meier, Matthias M M; Marty, Bernard

    2016-01-01

    We have measured the concentration, isotopic composition and thermal release profiles of Mercury (Hg) in a suite of meteorites, including both chondrites and achondrites. We find large variations in Hg concentration between different meteorites (ca. 10 ppb to 14'000 ppb), with the highest concentration orders of magnitude above the expected bulk solar system silicates value. From the presence of several different Hg carrier phases in thermal release profiles (150 to 650 {\\deg}C), we argue that these variations are unlikely to be mainly due to terrestrial contamination. The Hg abundance of meteorites shows no correlation with petrographic type, or mass-dependent fractionation of Hg isotopes. Most carbonaceous chondrites show mass-independent enrichments in the odd-numbered isotopes 199Hg and 201Hg. We show that the enrichments are not nucleosynthetic, as we do not find corresponding nucleosynthetic deficits of 196Hg. Instead, they can partially be explained by Hg evaporation and redeposition during heating of ...

  11. Detoxification of selenite and mercury by reduction and mutual protection in the assimilation of both elements by Pseudomonas fluorescens

    International Nuclear Information System (INIS)

    A study on the assimilation and detoxification of selenium and mercury and on the interaction between these two elements was conducted on Pseudomonas fluorescens. P. fluorescens was able to convert separately both elements to their elemental forms, which are less toxic and biologically less available. To study the converting mechanism of selenite to elemental Se, cells were grown in the presence of various selenite concentrations and several parameters such as extracellular protein concentrations, pH, carbohydrate concentrations, isocitrate dehydrogenase (ICDH) and malic enzyme were monitored. Transmission electron microscopy (TEM) and various analytical methods were applied to confirm the interaction between selenium and cell. The former appeared as a red precipitate localized predominantly in the consumed culture medium. P. fluorescens also resisted to the toxic effect of mercury by converting Hg2+ to the volatile and less toxic form Hg . Mercury reductase was likely responsible for the conversion of Hg2+ to Hg . More importantly, the interaction between mercury and selenium was also studied. The presence of selenite significantly reduced the accumulation of mercury in P. fluorescens. It was also interesting to note that mercury appeared to behave as a protecting agent against selenium intoxication as the bioaccumulation of Se was also inhibited by this metal. The formation of Se-Hg complexes could explain this mutual protective effect. No precipitate of elemental Se could be detected when Hg was present in the cultures

  12. Superheavy elements

    CERN Document Server

    Hofmann, S

    1999-01-01

    The outstanding aim of experimental investigations of heavy nuclei is the exploration of spherical 'SuperHeavy Elements' (SHEs). On the basis of the nuclear shell model, the next double magic shell-closure beyond sup 2 sup 0 sup 8 Pb is predicted at proton numbers between Z=114 and 126 and at neutron number N=184. All experimental efforts aiming at identifying SHEs (Z>=114) were negative so far. A highly sensitive search experiment was performed in November-December 1995 at SHIP. The isotope sup 2 sup 9 sup 0 116 produced by 'radiative capture' was searched for in the course of a 33 days irradiation of a sup 2 sup 0 sup 8 Pb target with sup 8 sup 2 Se projectiles, however, only cross-section limits were measured. Positive results were obtained in experiments searching for elements from 110 to 112 using cold fusion and the 1n evaporation channel. The produced isotopes were unambiguously identified by means of alpha-alpha correlations. Not fission, but alpha emission is the dominant decay mode. The measurement ...

  13. Seasonal and diurnal variations of Hg° over New England

    Directory of Open Access Journals (Sweden)

    J. D. Hegarty

    2008-03-01

    Full Text Available Factors influencing diurnal to interannual variability in Hg° over New England were investigated using multi-year measurements conducted by AIRMAP at the Thompson Farm (TF coastal site, an inland elevated site at Pac Monadnock (PM, and two month measurements on Appledore Island (AI in the Gulf of Maine. Mixing ratios of Hg° at TF showed distinct seasonality with maxima in March and minima in October. Hg° at AI tracked the trend at TF but with higher minima, while at PM the diurnal and annual cycles were dampened. In winter, Hg° was correlated most strongly with CO and NOy, indicative of anthropogenic emissions as their primary source. Our analysis indicates that Hg° had a regional background level of ~160 fmol/mol in winter, a dry deposition velocity of ~0.20 cm s−1 with a ~16 day lifetime in the coastal boundary layer in summer. The influence of oceanic emissions on ambient Hg° levels was identified using the Hg°-CHBr3 correlation at both TF and AI. Moreover, the lower Hg° levels and steeper decreasing warm season trend at TF (0.5–0.6 fmol/mol d−1 compared to PM (0.2–0.3 fmol/mol d−1 likely reflected the impact of marine halogen chemistry. Large interannual variability in warm season Hg° levels in 2004 versus 2005/2006 may be due to the role of precipitation patterns in influencing surface evasion of Hg°. In contrast, changes in wintertime maximum levels of Hg° were small compared to drastic reductions in CO, CO2, NOy, and SO2 from 2004/2005 to 2006/2007. These trends could be explained by a homogeneous distribution of Hg° over North American in winter due to its long lifetime and/or rapid removal of reactive mercury from anthropogenic sources. We caution that during warmer winters, the Hg°-CO slope possibly reflects Hg° loss relative to changes in CO more than their emission ratio.

  14. Seasonal and diurnal variations of Hg° over New England

    Directory of Open Access Journals (Sweden)

    J. D. Hegarty

    2007-11-01

    Full Text Available Factors influencing diurnal to interannual variability in Hg° over New England were investigated using multi-year measurements conducted by the AIRMAP program at the Thompson Farm (TF coastal site, an inland elevated site at Pac Monadnock (PM, and one summer of measurements on Appledore Island (AI in the Gulf of Maine. Mixing ratios of Hg° at TF showed distinct seasonality with maxima in March and minima in October. In comparison, Hg° at AI tracked the trend at TF but with higher minima, while at PM the diurnal and annual cycles were dampened. In winter, Hg° was correlated most strongly with CO and NOy, indicative of anthropogenic emissions as their primary source. Our analysis indicates that Hg° had a regional background level of ~160 fmol/mol, a summertime dry deposition velocity of ~0.20 cm s−1, and a ~16 day lifetime in the coastal boundary layer. The influence of oceanic emissions on ambient Hg° levels was identified using the Hg°-CHBr3 correlation at both TF and AI. Moreover, the lower Hg° levels and steeper decreasing warm season trend at TF (0.5–0.6 fmol/mol d−1 compared to PM (0.2–0.3 fmol/mol d−1 likely reflected the impact of marine halogen chemistry. Large interannual variability in warm season Hg° levels in 2004 versus 2005/2006 may be due to the role of precipitation patterns in influencing surface evasion of Hg°. In contrast, changes in wintertime maximum levels of Hg° were small compared to drastic reductions in CO, CO2, NOy, and SO2 from 2004/2005 to 2006/2007. These trends could be explained by a homogeneous surface distribution of Hg° over the North American continent in winter and/or rapid removal of mercury released from anthropogenic sources. We caution that during warmer winters, the Hg°-CO slope possibly reflects the ratio of Hg° loss relative to changes in CO more than their emission ratio.

  15. 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.

  16. Wading bird guano contributes to Hg accumulation in tree island soils in the Florida Everglades.

    Science.gov (United States)

    Zhu, Yingjia; Gu, Binhe; Irick, Daniel L; Ewe, Sharon; Li, Yuncong; Ross, Michael S; Ma, Lena Q

    2014-01-01

    Tree islands are habitat for wading birds and a characteristic landscape feature in the Everglades. A total of 93 surface soil and 3 soil core samples were collected from 7 degraded/ghost and 34 live tree islands. The mean Hg concentration in surface soils of ghost tree islands was low and similar to marsh soil. For live tree islands, Hg concentrations in the surface head region were considerably greater than those in mid and tail region, and marsh soils. Hg concentrations in bird guano (286 μg kg(-1)) were significantly higher than those in mammal droppings (105 μg kg(-1)) and plant leaves (53 μg kg(-1)). In addition, Hg concentrations and δ(15)N values displayed positive correlation in soils influenced by guano. During 1998-2010, estimated annual Hg deposition by guano was 148 μg m(-2) yr(-1) and ~8 times the atmospheric deposition. PMID:24080244

  17. Magnetically recoverable fluorescence chemosensor for the adsorption and selective detection of Hg2+ in water.

    Science.gov (United States)

    Lv, Qiang; Li, Gang; Cheng, Zhuhong; Lu, Hong; Gao, Xiaoxia

    2014-01-01

    In order to conveniently and effectively detect the heavy metal ion Hg(2+) existing in water, a magnetic fluorescence chemosensor has been strategically prepared by immobilizing a Rhodamine B derivative RhB-tris(2-aminoethyl)amine on Fe3O4@SiO2-Au@PSiO2 composites via gold particles. The adsorption and detection for Hg(2+) ions were investigated with fluorophotometry. This chemosensor shows high sensitivity and high selectivity for Hg(2+) over other metal cations owing to the ring opening of the rhodamine fluorophore selectively induced by Hg(2+). In addition, the presence of Fe3O4 in the sensor also facilitates the magnetic separation of the Fe3O4@SiO2-Au-Hg(2+)@PSiO2 from the solution. PMID:24270323

  18. X-ray photoelectron spectroscopic investigations of modifications in plasmid DNA after interaction with Hg nanoparticles

    International Nuclear Information System (INIS)

    The electronic structure of plasmid DNA both prior to and after its conjugation with Hg nanoparticles (NP) has been investigated here. The DNA molecules undergo severe perturbation on their interaction with Hg-NP. The circular plasmid DNA becomes predominantly linearised on interaction with 10 mM Hg salt solution. These perturbations are also reflected in the electronic structure of C1s and O1s suggesting severe modifications in the exocyclic groups, of the nucleic acid bases, participating in the hydrogen bondings. The results reflect the rupturing of the purine-pyrimidine bonds after interaction with the NP. The study also suggests selective and specific interactions of DNA bases with the Hg nanoparticles leading to the formation of metal-purine-pyrimidine complexes through rupturing of G-C base pairs. Hg-NP exclusively interact with the nitrogen bases of the DNA molecule and do not cause any significant modification to the phosphate backbone of DNA.

  19. Synthesis of Starch-Stabilized Ag Nanoparticles and Hg2+Recognition in Aqueous Media

    Directory of Open Access Journals (Sweden)

    Fan Yingju

    2009-01-01

    Full Text Available Abstract The starch-stabilized Ag nanoparticles were successfully synthesized via a reduction approach and characterized with SPR UV/Vis spectroscopy, TEM, and HRTEM. By utilizing the redox reaction between Ag nanoparticles and Hg2+, and the resulted decrease in UV/Vis signal, we develop a colorimetric method for detection of Hg2+ion. A linear relationship stands between the absorbance intensity of the Ag nanoparticles and the concentration of Hg2+ion over the range from 10 ppb to 1 ppm at the absorption of 390 nm. The detection limit for Hg2+ions in homogeneous aqueous solutions is estimated to be ~5 ppb. This system shows excellent selectivity for Hg2+over other metal ions including Na+, K+, Ba2+, Mg2+, Ca2+, Fe3+, and Cd2+. The results shown herein have potential implications in the development of new colorimetric sensors for easy and selective detection and monitoring of mercuric ions in aqueous solutions.

  20. Thermal radiation and low-temperature-vapour growth of HgI 2 crystal in production furnace

    Science.gov (United States)

    Roux, A.; Fedoseyev, A.; Roux, B.

    1993-06-01

    Heat exchanges in a sealed ampoule in the LTVG (low temperature vapour growth) furnace have been modelled in order to compute temperature fields and control the growth of HgI 2 crystals from vapour phase at low temperatures. We use a coupled conductive-radiative model to determine the shapes of the source and the crystal at different equilibrium states (i.e. without growth rate). The model involves conductivity anisotropy in the crystal and radiative exchanges between grey and diffuse surfaces (source and crystal interfaces, Pyrex walls), which are considered as opaque. Internal buoyancy effect is not taken into account as the pressure inside the ampoule is very small. The source temperature is fixed. For different undercoolings, i.e. for different cold finger temperatures, the "equilibrium" isotherm between the source/gas and crystal/gas interface has been numerically obtained. This "equilibrium" isotherm, which is associated with the stop of the growing process, gives a crystal shape. This shape is compared with experimental results given by the ETH-Zürich group. The model would permit a better understanding and control of the future HgI 2 crystal growth experiment. The computations are performed using a finite element package (FIDAP).

  1. Conductive-radiative model for predicting the shape of HgI2 crystal grown in the LTVG furnace

    Science.gov (United States)

    Roux, A.; Fedoseyev, A.; Roux, Bernard

    1992-08-01

    The modeling of heat exchanges in a sealed ampoule in the LTVG (Low Temperature Vapor Growth) furnace is focused upon, in order to compute temperature fields and control the growth of HgI2 crystals from vapor phase at low temperatures. A coupled conductive radiative model was used to determine the shape of the source and the crystal at different equilibrium states (that is, without growth rate). The model involves conductivity anisotropy in the crystal and radiative exchanges between grey and diffuse surfaces (source and crystal interfaces, pyrex walls), which are considered as opaque. Internal buoyancy effect is not taken into account as the pressure inside the ampoule is very small. The source temperature is fixed. For different undercoolings, that is, for different cold finger temperatures, the 'equilibrium' isotherm between the source/gas and crystal/gas interfaces was numerically obtained. This 'equilibrium' isotherm, which is associated with the stop of the growing process, gives a crystal shape. This shape is compared with experimental results given by the ETH-Zurich group. The model would permit a better understanding and control of the future HgI2 crystal growth experiment. The computations are performed using a finite element package (FIDAP).

  2. Synthesis, Characterization and Thermal Analysis of a New Acetic Acid (2-Hydroxy-benzylidene-hydrazide and its Complexes with Hg(II and Pd(II

    Directory of Open Access Journals (Sweden)

    Hajar Sahebalzamani

    2011-01-01

    Full Text Available The new complexes have been synthesized by the reaction of Hg(II and Pd(II with acetic acid(2-hydroxy-benzylidene- hydrazide (L. These new complexes were characterized by elemental analysis, IR, H NMR spectroscopy and UV spectral techniques. The changes observed between the FT-IR, H NMR and UV-Vis spectra of the ligands and of the complexes allowed us to establish the coordination mode of the metal in complexes. Thermal properties, TG-DTA of these complexes were studied. TG- DTA and other analytical methods have been applied to the investigation of the thermal behavior and structure of the compounds [M(L2]Cl2 M= Hg, Pd. Thermal decomposition of these compounds is multi-stage processes.

  3. Dislocation reduction in HgCdTe grown on CdTe/Si

    Science.gov (United States)

    Wijewarnasuriya, Priyalal S.

    2016-05-01

    Bulk-grown CdZnTe (Zn = 3%) substrates are the natural choice for HgCdTe epitaxy since it is lattice matched to long wave LW-HgCdTe alloy. However, lack of large area CdZnTe substrates, high production costs, and more importantly, the difference in thermal expansion coefficients between CdZnTe and silicon Read out Integrated Circuits (ROIC) are some of the inherent drawbacks of CdZnTe substrates. Consequently, Hg1-xCdxTe detectors fabricated on silicon substrates are an attractive alternative. Recent developments in the molecular beam epitaxy (MBE) buffer layer growth technology on Si substrates has revolutionized the HgCdTe research and offered a new dimension to HgCdTe-based IR technology. Si substrates provide advantages in terms of relatively large area (3 to 6-inch diameter is easily obtained) compared to CZT substrate materials, durability during processing, and reliability to thermal cycling. Innovations in Si-based composite substrates made it possible to fabricate very large-format IR arrays that offer higher resolution, low-cost arrays and more dies per wafer. Between Si substrates and HgCdTe has large lattice mismatch of 19%. This leads to dislocation densities of low-107 cm-2 for optimal growth of HgCdTe on silicon-based substrates as compared to the mid-104 cm-2 dislocation density of HgCdTe grown on CdZnTe. This paper present dislocation reduction by two orders of magnitude using thermal cycle anneal under Hg environment on HgCdTe grown on Si substrates and as well as defect reduction in Cd(Se)Te buffer layers grown on Si Substrates.

  4. Ion permeation of AQP6 water channel protein. Single channel recordings after Hg2+ activation.

    Science.gov (United States)

    Hazama, Akihiro; Kozono, David; Guggino, William B; Agre, Peter; Yasui, Masato

    2002-08-01

    Aquaporin-6 (AQP6) has recently been identified as an intracellular vesicle water channel with anion permeability that is activated by low pH or HgCl2. Here we present direct evidence of AQP6 channel gating using patch clamp techniques. Cell-attached patch recordings of AQP6 expressed in Xenopus laevis oocytes indicated that AQP6 is a gated channel with intermediate conductance (49 picosiemens in 100 mm NaCl) induced by 10 microm HgCl2. Current-voltage relationships were linear, and open probability was fairly constant at any given voltage, indicating that Hg2+-induced AQP6 conductance is voltage-independent. The excised outside-out patch recording revealed rapid activation of AQP6 channels immediately after application of 10 microm HgCl2. Reduction of both Na+ and Cl- concentrations from 100 to 30 mm did not shift the reversal potential of the Hg2+-induced AQP6 current, suggesting that Na+ is as permeable as Cl-. The Na+ permeability of Hg2+-induced AQP6 current was further demonstrated by 22Na+ influx measurements. Site-directed mutagenesis identified Cys-155 and Cys-190 residues as the sites of Hg2+ activation both for water permeability and ion conductance. The Hill coefficient from the concentration-response curve for Hg2+-induced conductance was 1.1 +/- 0.3. These data provide the first evidence of AQP6 channel gating at a single-channel level and suggest that each monomer contains the pore region for ions based on the number of Hg2+-binding sites and the kinetics of Hg2+-activation of the channel. PMID:12034750

  5. Synthesis and characterization of ZnxHg1-xSeyS1-y quantum dots

    International Nuclear Information System (INIS)

    This article describes the synthesis of highly water-soluble ZnxHg1-xSeyS1-y quantum dots (QDs) in aqueous solution through a simple photo-assisted reaction between ZnSe QDs and mercury(I) nitrate dihydrate [Hg2(NO3)2.2H2O]. In order to deduce the optimal synthesis conditions, we varied several parameters, including the concentrations of mercaptosuccinic acid (MSA) and Hg2(NO3)2.2H2O, the illumination time, and the reaction temperature. When irradiated at temperatures below 80 oC, the ZnSe QDs reacted with the S2- ions formed rapidly from MSA and the Hg2+ ions formed from Hg22+ ions to form ZnxHg1-xSeyS1-y QDs through a process of photo-etching and surface combination. Under different conditions, we prepared a series of ZnxHg1-xSeyS1-y QDs that emit fluorescence at the maximum wavelengths ranging from 405 to 760 nm. Inductively coupled plasma-mass spectrometry and transmission electron microscopy/energy dispersive spectrometry revealed that the content of Hg in the ZnxHg1-xSeyS1-y QDs was greater when the synthesis was conducted at higher temperature. The Zn0.88Hg0.12Se0.44S0.56 QDs exhibit improved photostability than crude ZnSe QDs and possess long lifetimes (τ1 ∼ 38 ns and τ2 ∼ 158 ns).

  6. Reproducible Design for the Optical Screening and Sensing of Hg(II Ions

    Directory of Open Access Journals (Sweden)

    Emad A. Elshehy

    2014-10-01

    Full Text Available We fabricated silica nanotubes with hexagonally ordered mesopores (6 nm inside a membrane disc with a uniform channel neck size of 200 nm and a longitudinal thickness of 60 μm to design an optical sensor membrane (OSM for the screening and sensing of extremely toxic Hg(II ions. The optical detection and quantitative recognition of Hg(II ions in water were conducted even at trace concentrations without the need for sophisticated instruments. The OSM design was based on the physical interaction of a responsive organic probe with silica pore surfaces followed by strong and selective binding Hg(II–probe interactions under specific sensing conditions, particularly at pH 5. Ultra-trace concentrations of Hg(II ions were easily detected with the naked eye using the OSM. The remarkable ion spectral response of Hg(II ion–OSM ensured the excellent quantification of the OSM for Hg(II ion sensing over a wide range of concentrations with a detection limit of 1.75 × 10−9 M. This result indicated that low concentrations of Hg(II ions can be detected with a high sensitivity. One of the key issues of OSM is the Hg(II ion-selective workability even in the presence of high doses of competitive matrices and species. The OSM design showed significant Hg(II ion-sensing capability despite the number of reuse/recycles using simple decomplexation. Given its high selectivity, fast response, and sensitivity, the OSM could be developed into a specific Hg(II ion-sensing kit in aqueous solutions.

  7. HG-AFS Determination of Selenium in Moringa Oleifera%HG-AFS测定辣木中的Se

    Institute of Scientific and Technical Information of China (English)

    黄国清; 肖仔君

    2007-01-01

    采用湿法消解,HG-AFS法(氢化物发生原子荧光光谱法)对辣木中微量Se含量进行了分析测定,系统地考察了消化方式、仪器工作条件、酸介质、掩蔽剂等因素对测定的影响,确定了最佳测定条件,结果表明:方法的最低检出限为0.42 ng·mL-1,线性范围0~120 ng·mL-1,相对标准偏差(RSI))为3·53%(n=11),回收率为95.2%~104.6%,表明该方法有较高灵敏度,并且简便、快速、准确.

  8. Elemental bioaccumulators in air pollution studies

    International Nuclear Information System (INIS)

    K0-Based instrumental neutron activation analysis (k0 INAA) was used to determine the concentrations of Cr, Fe, Co, Zn, Se, Sb and Hg in the vascular plants Cistus salvifolius and Inula viscosa and in the lichen Parmelia sulcata. The samples were collected in the neighbourhood of industrial complexes. The elemental accumulation in the vascular plants and the lichen are compared to optimize the choice of the bioaccumulator. It is concluded that P.sulcata seems to be the best accumulator of the three species for the element studied; Cistus salvifolius is sensitive to the contents of Zn, Fe, Cr and Sb in the air; Inula viscosa seems to accumulate Fe, Sb, Co, Cr and Zn. Nevertheless, it is concluded that lichen is a good air pollution indicator, while the vascular plants are not due to the large seasonal variations found in the elemental concentrations. (author) 11 refs.; 7 figs.; 2 tabs

  9. Trace elements in two odontocete species (Kogia breviceps and Globicephala macrorhynchus) stranded in New Caledonia (South Pacific)

    International Nuclear Information System (INIS)

    Trace elements in whales on New Caledonia beaches are below levels for concern. - Liver, muscle and blubber tissues of two short-finned pilot whales (Globicephala macrorhynchus) and two pygmy sperm whales (Kogia breviceps) stranded on the coast of New Caledonia have been analysed for 12 trace elements (Al, Cd, Co, Cr, Cu, Fe, organic and total Hg, Mn, Ni, Se, V, and Zn). Liver was shown to be the most important accumulating organ for Cd, Cu, Fe, Hg, Se, and Zn in both species, G. macrorhynchus having the highest Cd, Hg, Se and Zn levels. In this species, concentrations of total Hg are particularly elevated, reaching up to 1452 μg g-1 dry wt. Only a very low percentage of the total Hg was organic. In both species, the levels of Hg are directly related to Se in liver. Thus, a molar ratio of Hg:Se close to 1.0 was found for all specimens, except for the youngest K. breviceps. Our results suggest that G. macrorhynchus have a physiology promoting the accumulation of high levels of naturally occurring toxic elements. Furthermore, concentrations of Ni, Cr and Co are close to or below the detection limit in the liver and muscles of all specimens. This suggests that mining activity in New Caledonia, which typically elevates the levels of these contaminants in the marine environment, does not seem to be a significant source of contamination for these pelagic marine mammals

  10. Spins of superdeformed band in {sup 192}Hg

    Energy Technology Data Exchange (ETDEWEB)

    Lauritsen, T.; Khoo, T.L.; Henry, R.G. [and others

    1995-08-01

    Determination of the spins of SD states is the most important challenge in the study of superdeformation. Knowledge of the spin will provide crucial information on SD bands, in particular on the fascinating phenomenon of bands with identical energies and moments of inertia. Angular distribution coefficients of the {gamma}rays decaying out of the {sup 192}Hg SD band were determined using Eurogam data. These coefficients, as well as the spectral shape and multiplicity of the spectrum, are compared with the results of calculations, thereby providing a check on these calculations. From the measured decay multiplicity and the calculated average spin removed per photon (0.3 h), we deduce the average spin {bar I}{sub decay} removed by the {gamma} rays connecting SD and normal states. The spin I{sub SD} of the SD band from which the decay occurs is given by I{sub SD} = {bar I} decay + {bar I} ND, where {bar I} ND is the average spin removed by the normal yrast states. The state from which the major decay out of the SD band occurs is found to have spin 9.5 {plus_minus} 0.8 h. Since angular momentum is (quantized), this leads to a spin assignment of 9 or 10 h. The latter value is favored since the yrast band in the SD well must have only even spin values. This constitutes the first deduction of spin from data in the mass 150 and 190 regions. The spin of 10 h agrees with the spin which is inferred from a model, using the observed moment of inertia (Im){sup (2)}{omega}.

  11. Assessment of the content of mercury, methylmercury and other elements of interest in fish, hair and diets of pre-school children of the Amazon region

    International Nuclear Information System (INIS)

    Studies show that some regions of the Amazon region suffer mercury (Hg) impacts as a direct result of both natural and anthropogenic processes. Jau National Park (PNJ) is the only National Park in Brazil that protects an entire black water basin (Jau River), flood land and tropical reserve. These conditions favor Hg methylation in the aquatic biota. This in turn, exposes living on the river populations to Hg contamination as well as the adjacent regions. Preliminary studies of pre-school children diets from PNJ communities have shown that these diets have a worrisome high Hg content. The present study assessed total Hg content, micro nutrients (Ca, Fe, K, Na, Se and Zn) and macro nutrients (proteins, lipids, ash, energy, carbohydrate) in pre-school diets in the PNJ and surrounding communities. Furthermore, total and Me Hg levels were also determined in hair samples of these children as well as those living in several neighborhoods of the city of Manaus. Included in this determination were the fish most consumed by these populations. From these results it was possible to evaluate the nutritional content of the diets and the exposure of the children to Hg and Se Hg. Cold vapor atomic absorption spectrometry was used to quantify total and Me Hg. Micro nutrient determination was performed using neutron activation analysis technique (NAA) and Macro nutrient through AOAC methodologies (USA). All analytical methods were developed and validated for precision and accuracy by means of reference materials analyses with certified values for the determined elements. Furthermore, the uncertainty sources for Hg and Me Hg determination were assessed and the expanded uncertainties were calculated. Total Hg levels in diets and total and Me Hg levels for hair samples, were well above those values found in different localities of the Amazon region. This also holds true for those surrounding areas of the JNP. For many children Hg intake values passed the 5 mug Hg/body weigh/week (PTWI

  12. The role of iodine monochloride for the oxidation of elemental mercury

    Energy Technology Data Exchange (ETDEWEB)

    Qu Zan [School of Environmental Science and Engineering, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai 200240 (China); Yan Naiqiang, E-mail: nqyan@sjtu.edu.cn [School of Environmental Science and Engineering, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai 200240 (China); Liu Ping; Jia Jinping; Yang Shijian [School of Environmental Science and Engineering, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai 200240 (China)

    2010-11-15

    The removal of Hg{sup 0} by the homogenous gas-phase reaction and particle-induced reaction was investigated under various conditions. Iodine monochloride was found to be efficient for Hg{sup 0} oxidation, with the apparent 2nd-order rate constant of about 10.5({+-}0.3) x 10{sup -17} cm{sup 3} molecules{sup -1} s{sup -1} and 5.7({+-}0.3) x 10{sup -17} cm{sup 3} molecules{sup -1} s{sup -1} at 273 K and 373 K, respectively. The pilot-scale tests showed that the removal of Hg{sup 0} by ICl increased significantly in presence of flyash. It was predicted that over 90% of Hg{sup 0} removal efficiency can be obtained with 0.2 ppmv ICl and 20 g/m{sup 3} flyash in flue gas. Though the reaction between Hg{sup 0} and ICl was by far faster than that of Hg{sup 0}/Cl{sub 2}, the major product was found to be HgCl{sub 2} rather than HgI{sub 2}, which implicated that iodine might partly act as the accelerant in Hg{sup 0} oxidation by facilitating the formation of certain intermediates. The results indicated that using ICl to oxidize elemental mercury in coal-fired flue gas can save the consumption of iodine, and it appeared to be a promising oxidant to enhance the removal of Hg{sup 0}.

  13. Influence of gas components on the oxidation of elemental mercury by positive pulsed corona discharge

    Energy Technology Data Exchange (ETDEWEB)

    Ko, KB.; Byun, Y.; Cho, M.; Namkung, W.; Hamilton, I.P.; Shin, D.N.; Koh, D.J.; Kim, K.T. [Research Institute for Industrial Science and Technology, Pohang (Republic of Korea)

    2008-07-01

    This study examines the effect of flue gas components on the oxidation of gaseous elemental mercury (Hg{sup 0}) to Hg{sup O} and HgCl{sub 2} via pulsed corona discharge (PCD), where the reaction temperature was set to 90 degrees C and the gas stream consisting of 3% H{sub 2}O and 10% O{sub 2} in N{sub 2} was mixed with 45 mu g m{sup -3} Hg{sup 0}, 108 ppm NOx, 80 ppm HCl, 200 ppm SO{sub 2} and 470 ppm NH{sub 3}. It has been observed that O{sub 2} and HCl components in the gas stream act as oxidizing precursors through the generation of oxidizing species (O, O{sub 3}, Cl and Cl{sub 2}) in the PCD process. The presence of NO directly hampers Hg{sup 0} oxidation to Hg{sup O} due to preferential reaction of NO with O and O{sub 3}. In contrast, the presence of SO{sub 2} indirectly influences the oxidation of Hg{sup 0} to HgCl{sub 2} through the fast reaction of SO{sub 2} with OH radical, resulting in consuming OH radicals which are partially responsible for the formation of chlorine species, I. e. Cl and Cl{sub 2}. It has been also found that NH{sub 3} component significantly hinders the oxidation of Hg{sup 0} to HgCl{sub 2} through the fast acid-base reaction with HCl.

  14. Influence of HCl on oxidation of gaseous elemental mercury by dielectric barrier discharge process.

    Science.gov (United States)

    Ko, Kyung Bo; Byun, Youngchul; Cho, Moohyun; Namkung, Won; Shin, Dong Nam; Koh, Dong Jun; Kim, Kyoung Tae

    2008-04-01

    The influence of HCl on the oxidation of gaseous elemental mercury (Hg0) has been investigated using a dielectric barrier discharge (DBD) plasma process, where the temperature of the plasma reactor and the composition of gas mixtures of HCl, H2O, NO, and O2 in N2 balance have been varied. We observe that Cl atoms and Cl2 molecules, created by the DBD process, play important roles in the oxidation of Hg0 to HgCl2. The addition of H2O to the gas mixture of HCl in N2 accelerates the oxidation of Hg0, although no appreciable effect of H2O alone on the oxidation of Hg0 has been observed. The increase of the reaction temperature in the presence of HCl results in the reduction of Hg0 oxidation efficiency probably due to the deterioration of the heterogeneous chemical reaction of Hg0 with chlorinated species on the reactor wall. The presence of NO shows an inhibitory effect on the oxidation of Hg0 under DBD of 16% O2 in N2, indicating that NO acts as an O and O3 scavenger. At the composition of Hg0 (280 microg m(-3)), HCl (25 ppm), NO (204 ppm), O2 (16%) and N2 (balance) and temperature 90 degrees C, we obtain the nearly complete oxidation of Hg0 at a specific energy density of 8 J l(-1). These results lead us to suggest that the DBD process can be viable for the treatment of mercury released from coal-fired power plants. PMID:18313101

  15. Mercury speciation and total trace element determination of low-biomass biological samples.

    Science.gov (United States)

    Taylor, Vivien F; Jackson, Brian P; Chen, Celia Y

    2008-12-01

    Current approaches to mercury speciation and total trace element analysis require separate extraction/digestions of the sample. Ecologically important aquatic organisms--notably primary consumers such as zooplankton, polychaetes and amphipods--usually yield very low biomass for analysis, even with significant compositing of multiple organisms. Individual organisms in the lower aquatic food chains (mussels, snails, oysters, silversides, killifish) can also have very low sample mass, and analysis of whole single organisms is important to metal uptake studies. A method for the determination of both methyl Hg and total heavy metal concentrations (Zn, As, Se, Cd, Hg, Pb) in a single, low-mass sample of aquatic organisms was developed. Samples (2 to 50 mg) were spiked with enriched with (201)MeHg and (199)Hg, then leached in 4 M HNO(3) at 55 degrees C for extraction of MeHg. After 16 h, an aliquot (0.05 mL) was removed to determine mercury species (methyl and inorganic Hg) by isotope dilution gas chromatography inductively coupled plasma mass spectrometry (ICP-MS). The leachate was then acidified to 9 M HNO(3) and digested in a microwave at 150 degrees C for 10 min, and total metal concentrations were determined by collision cell ICP-MS. The method was validated by analyzing five biological certified reference materials. Average percent recoveries for Zn, As, Se, Cd, MeHg, Hg(total) and Pb were 99.9%, 103.5%, 100.4%, 103.3%, 101%, 97.7%, and 97.1%, respectively. The correlation between the sum of MeHg and inorganic Hg from the speciation analysis and total Hg by conventional digestion of the sample was determined for a large sample set of aquatic invertebrates (n = 285). Excellent agreement between the two measured values was achieved. This method is advantageous in situations where sample size is limited, and where correlations between Hg species and other metals are required in the same sample. The method also provides further validation of speciation data, by

  16. Ultrasonic-assisted synthesis and structural characterization of two new nano-structured Hg(II) coordination polymers.

    Science.gov (United States)

    Ghasempour, Hosein; Azhdari Tehrani, Alireza; Morsali, Ali

    2015-11-01

    Two new Hg(II) coordination polymers containing N,N'-Bis-pyridin-3-ylmethylene-naphtalene-1,5-diamine ligand were synthesized by conventional and sonochemical methods, characterized by spectroscopic techniques (FT-IR and elemental analysis), and their X-ray crystallographic structures were determined. The crystal packing and supramolecular features of these coordination polymers were studied using geometrical analysis and Hirshfeld surface analysis. The crystal structure analysis revealed that H⋯H contacts, C-H⋯π and C-H⋯X (X = Cl for 1 and X = Br for 2) hydrogen bonding interactions are strong enough to govern the supramolecular architecture. The BFDH analysis helps us to compare the predicted morphology to that obtained under ultrasonication. This study may provide further insight into discovering the role of weak intermolecular interactions in the context of nano-supramolecular assembly.

  17. Experimental analysis of the simultaneous uptake of the heavy metals Cd, Hg, Pb, Cu, Zn, Se in the sporophore of mushrooms. Versuche ueber die simultane Aufnahme der Schwermetalle Cd, Hg, Pb, Cu, Zn und Se in Pilzfruchtkoerper

    Energy Technology Data Exchange (ETDEWEB)

    Suehs, K.

    With mushrooms of the species Agaricus bisporus and Boletus badius the simultaneous uptake of the heavy metals Cd, Hg, Pb, Cu, Zn, and Se from soil to the sporophore was studied. To avoid misleadingly overrated enrichmentfactors when comparing the heavy metal contents of dried mushrooms and soils, a so-called transfer factor TF[sub v] which is related to the volume is put to discussion here, this factor takes account of the relatively small amount of dry matter in mushrooms and of the different composition (that means specific weight) of the soils in question. With help of these transfer factors the conclusion is derived, that essential elements show a better enrichment behaviour than biologically superfluous heavy metals, at least this is true with the insignificantly contaminated soils we investigated. With Cd as an example of a ''superfluous'' element it is shown that there is a strict proportionality of Cd concentrations in the mushrooms and the corresponding soils, thus producing a constant transfer factor. Apart from this the uptake of copper into the mushrooms is promoted (growth of the transfer factor) by a larger Cd supply, whereas the other elements under investigation (even the classical antagonist Zn) are not significantly affected. Furthermore there is evidence that with increasing heavy metal concentration (Cd) first the fructification of the thallus is supported and moreover, that increasing age of this primary fungus corresponds with an increase of heavy metals in the mushrooms. (orig.)

  18. Organ-specific accumulation, transportation, and elimination of methylmercury and inorganic mercury in a low Hg accumulating fish.

    Science.gov (United States)

    Peng, Xiaoyan; Liu, Fengjie; Wang, Wen-Xiong

    2016-08-01

    Low mercury (Hg) concentrations down to several nanograms Hg per gram of wet tissue are documented in certain fish species such as herbivorous fish, and the underlying mechanisms remain speculative. In the present study, bioaccumulation and depuration patterns of inorganic Hg(II) and methylmercury (MeHg) in a herbivorous rabbitfish Siganus canaliculatus were investigated at organ and subcellular levels following waterborne or dietary exposures. The results showed that the efflux rate constants of Hg(II) and MeHg were 0.104 d(-1) and 0.024 d(-1) , respectively, and are probably the highest rate constants recorded in fish thus far. The dietary MeHg assimilation efficiency (68%) was much lower than those in other fish species (∼90%). The predominant distribution of MeHg in fish muscle was attributable to negligible elimination of MeHg from muscle (< 0) and efficient elimination of MeHg from gills (0.12 d(-1) ), liver (0.17 d(-1) ), and intestine (0.20 d(-1) ), as well as efficient transportation of MeHg from other organs into muscle. In contrast, Hg(II) was much more slowly distributed into muscle but was efficiently eliminated by the intestine (0.13 d(-1) ). Subcellular distribution indicated that some specific membrane proteins in muscle were the primary binding pools for MeHg, and both metallothionein-like proteins and Hg-rich granules were the important components in eliminating both MeHg and Hg(II). Overall, the present study's results suggest that the low tissue Hg concentration in the rabbitfish was partly explained by its unique biokinetics. Environ Toxicol Chem 2016;35:2074-2083. © 2016 SETAC. PMID:26756981

  19. Toxic element concentrations in the Razorbill Alca torda (Charadriiformes, Alcidae) in Portugal.

    Science.gov (United States)

    Ribeiro, A R; Eira, C; Torres, J; Mendes, P; Miquel, J; Soares, A M V M; Vingada, J

    2009-04-01

    The present study provides the first data on inorganic element levels (As, Cd, Co, Cr, Cu, Hg, Mn, Pb, Se, and Zn) in juvenile, immature, and adult razorbills (Alca torda) collected along the central coast of Portugal. Element concentrations were assessed by ICP-MS in kidney, liver, muscle, and feathers of 28 razorbills, including 4 juveniles, 17 subadults, and 7 adults. The effect of age and tissue on element accumulation was also assessed. The detected levels in razorbills may indicate a possible contamination risk by Hg and Cr. With respect to bird tissues, higher accumulation of Se and Cd was detected in kidney, Zn and Pb in feathers, and As and Mn in liver. Age was found to affect the accumulation of Cd, Cr, Cu, Hg, and Mn, juveniles presenting higher levels of Cu and Mn than older individuals. In razorbill kidney, Zn-Hg constituted the most significant relationship among metal concentrations. Liver presented the highest number of significant relationships (mostly involving Zn and Co). With regard to feathers, the most significant relationships involved Se, Zn, Cr and Cu concentrations. Positive linear relationships were detected among kidney, liver, and muscle, with emphasis on relationships involving Se and Hg, which may be indicative of similar accumulation/regulation mechanisms in those organs. Element concentrations are discussed in view of possible detoxification mechanisms in seabirds.

  20. Synthesis of N,N,N-4,4"-Di-(4-methylphenyl)-2,2':6',2"-terpyridine-N,N,N-tris(isothiocyanato) Ruthenium(Ⅱ) and Application to Colorimetric Hg2+ Sensor

    Institute of Scientific and Technical Information of China (English)

    LI Xiang-Hong; LIU Zhi-Qiang; LI Fu-You; DUAN Xin-Fang; HUANG Chun-Hui

    2007-01-01

    A terpyridine derivative DPTP [di-(4-methylphenyl)-2,2':6',2"-terpyridine] was conveniently synthesized from 2-bromopyridine via halogen-dance reaction, Kharash coupling and Stille coupling reaction. Then its corresponding ruthenium complex Ru-DPTP [N,N,N-4,4"-di-(4-methylphenyl)-2,2':6',2"-terpyridine-N,N,N-tris(iso-thiocyanato)-ruthenium(Ⅱ) ammonium] was obtained and fully characterized by IR, UV-Vis, ESI MS and elemental analysis. The MLCT absorption band of Ru-DPTP was blue-shifted from 570 to 500 nm upon addition of Hg2+. Among a series of surveyed metal ions, the complex showed a unique recognition to Hg2+, indicating that it can be used as a selective colorimetric sensor for Hg2+.

  1. The vertical photoconductor: A novel device structure suitable for HgCdTe two-dimensional infrared focal plane arrays

    Science.gov (United States)

    Siliquini, J. F.; Faraone, L.

    1997-06-01

    A novel photoconductive device structure is proposed and described that has been designed specifically as a sensing element for high density two-dimensional infrared focal plane array (IRFPA) applications. Although the design concept can be applied to a variety of epitaxially grown HgCdTe material, optimum performance can be achieved using n-type HgCdTe semiconductor material consisting of epitaxially grown heterostructure layers in which a two-dimensional mosaic of vertical design photoconductors are fabricated. The heterostructure layers provide high performance devices at greatly reduced power dissipation levels, while the vertical design allows for the high density integration of photoconductors in a two-dimensional array geometry with high fill factor. The salient feature of the proposed device structure is that the bias field is applied in the vertical direction such that it is parallel to the impinging infrared radiation. A comprehensive one-dimensional model is presented for the vertical design photoconductor, which is subsequently used to determine the optimum design parameters in order to achieve maximum responsivity at the lowest possible power dissipation level. It is found that the proposed device structure has the potential to be used in the fabrication of long wavelength IRFPAs approaching 10 6 pixels using 25 × 25 μm 2 detector elements. Furthermore, this is achieved with individual device detectivities that are background limited and for a total array power dissipation of less than 0.1 W using a pulsed biasing scheme. Performance issues such as response uniformity, pixel yield, fill factor, crosstalk, power dissipation, detector impedance, array architecture, and maximum array size are discussed in relation to the suitability of the proposed vertical photoconductor structure for use in IRFPA modules. When considering IRFPA operability, it is found that in many cases the proposed technology has the potential to deliver significant advantages, such

  2. The thermal release of HG from chondrites and their thermal histories

    Science.gov (United States)

    Jovanovic, S.; Reed, G. W.

    1985-08-01

    A quantitative treatment and implications of isothermal and linear heating data on Hg in meteorites are given as a sequel to a more qualitative analysis of meteorite thermal histories (Reed and Jovanovic, 1968). Studies of Hg in terrestrial metamorphic rocks establish that thermal events to which meteorites were subjected fall in the same temperature range, of 400-900 C, as exists during terrestrial metamorphism. Hg diffusion parameters based on data from the linear and isothermal heating experiments are calculated. The conclusions are: (1) Meteorites experienced thermal events of the same magnitude as those measured by primarily mineralogical metamorphic indicators reviewed by Dodd (1969); (2) no correspondence with mineralogical-petrological metamorphic grade is evident; (3) Hg data for some chondrites correlate with shock facies (non-thermal) indicators (Dodd and Jarosewich, 1979); (4) small Hg activation energies (6-14 kcal/mole) require that the meteorites must have been stored in closed systems until low temperatures were attained. Hg must be presented as an involatile mineral(s) or as a substituent in a host phase at temperatures below 100 C. Consistent with this interpretation is the fact that despite diffusion times of 100-1,000,000 years at 200 K, Hg was retained in small objects over cosmic ray exposure periods of a hundred-million years.

  3. The longitudinal translocation characters and the influencing factors of Hg, Cd in the soil

    Directory of Open Access Journals (Sweden)

    Zhang Yujuan

    2006-11-01

    Full Text Available Combining the methods of simulation test and field survey, the longitudinal distribution and the influencing factors of Hg and Cd in the profile in the typical sewage irrigation area were studied in this paper and the result shows: (1 the content distribution of Hg, Cd in the superficial soil profile was higher than that in the bottom and the content decreased with the increase of the depth, the translocation ability of the Hg, Cd in the garden mould and cinnamon soil were lower than that in the paddy soil and fluve-aquic soil, the longitudinal translocation ability of the Cd in the soil profile was stronger than that of Hg; (2 Hg was accumulated in the different soil and has the highest accumulation rate in the paddy soil and the lowest in the cinnamon soil; the translocation order of the Cd in the different was: garden mould > paddy soil > cinnamon soil > fluve-aquic soil; (3 the concentration of Hg, Cd in the soil leacheate increased with the concentration increase of Hg, Cd in the sewage, the migration rate increased with the roughness of the soil quality and decreased with the increase of pH and soil organic matter.

  4. In Situ Behavioral Response of Common Loons Associated with Elevated Mercury (Hg Exposure

    Directory of Open Access Journals (Sweden)

    Philip D. Taylor

    1998-12-01

    Full Text Available Common Loons (Gavia immer in Nova Scotia, Canada have the highest blood mercury (Hg concentrations of any loon population in North America. Previous studies have shown that exposure to varying levels of Hg in prey is associated with changes in pre-nesting adult behavior. We report here the first association of sublethal blood Hg contamination with changes in behavior of Common Loon young. As Hg levels in their blood rise, the amount of time that chicks spend brooding (by back-riding decreases (P = 0.004 and time spent preening increases (P = 0.003. The sum increase in energy expenditure is not being compensated for with expected increases in feeding rates or begging. We suggest that such altered time-activity budgets may disrupt the energetic balance of young. Our results show that variation in time spent back-riding is associated with changes in fledging rates. Adult behavior did not significantly vary with Hg, but results are suggestive that an association may exist. We also show that monitoring the time-activity budgets of very young chicks can serve to indicate the effects Hg concentrations in their blood. We confirm the hypothesis that loons and other upper trophic level predators could be at risk from elevated levels of bioavailable Hg. This may help to explain the chronically low productivity of such contaminated sites as Kejimkujik and allow for more focused management initiatives.

  5. Hg concentrations in fish from coastal waters of California and Western North America.

    Science.gov (United States)

    Davis, J A; Ross, J R M; Bezalel, S; Sim, L; Bonnema, A; Ichikawa, G; Heim, W A; Schiff, K; Eagles-Smith, C A; Ackerman, J T

    2016-10-15

    The State of California conducted an extensive and systematic survey of mercury (Hg) in fish from the California coast in 2009 and 2010. The California survey sampled 3483 fish representing 46 species at 68 locations, and demonstrated that methylHg in fish presents a widespread exposure risk to fish consumers. Most of the locations sampled (37 of 68) had a species with an average concentration above 0.3μg/gwet weight (ww), and 10 locations an average above 1.0μg/gww. The recent and robust dataset from California provided a basis for a broader examination of spatial and temporal patterns in fish Hg in coastal waters of Western North America. There is a striking lack of data in publicly accessible databases on Hg and other contaminants in coastal fish. An assessment of the raw data from these databases suggested the presence of relatively high concentrations along the California coast and in Puget Sound, and relatively low concentrations along the coasts of Alaska and Oregon, and the outer coast of Washington. The dataset suggests that Hg concentrations of public health concern can be observed at any location on the coast of Western North America where long-lived predator species are sampled. Output from a linear mixed-effects model resembled the spatial pattern observed for the raw data and suggested, based on the limited dataset, a lack of trend in fish Hg over the nearly 30-year period covered by the dataset. Expanded and continued monitoring, accompanied by rigorous data management procedures, would be of great value in characterizing methylHg exposure, and tracking changes in contamination of coastal fish in response to possible increases in atmospheric Hg emissions in Asia, climate change, and terrestrial Hg control efforts in coastal watersheds. PMID:27067833

  6. MeHg Suppressed Neuronal Potency of Hippocampal NSCs Contributing to the Puberal Spatial Memory Deficits.

    Science.gov (United States)

    Tian, Jianying; Luo, Yougen; Chen, Weiwei; Yang, Shengsen; Wang, Hao; Cui, Jing; Lu, Zhiyan; Lin, Yuanye; Bi, Yongyi

    2016-08-01

    Hippocampal neurogenesis-related structural damage, particularly that leading to defective adult cognitive function, is considered an important risk factor for neurodegenerative and psychiatric diseases. Normal differentiation of neurons and glial cells during development is crucial in neurogenesis, which is particularly sensitive to the environmental toxicant methylmercury (MeHg). However, the exact effects of MeHg on hippocampal neural stem cell (hNSC) differentiation during puberty remain unknown. This study investigates whether MeHg exposure induces changes in hippocampal neurogenesis and whether these changes underlie cognitive defects in puberty. A rat model of methylmercury chloride (MeHgCl) exposure (0.4 mg/kg/day, PND 5-PND 33, 28 days) was established, and the Morris water maze was used to assess cognitive function. Primary hNSCs from hippocampal tissues of E16-day Sprague-Dawley rats were purified, identified, and cloned. hNSC proliferation and differentiation and the growth and morphology of newly generated neurons were observed by MTT and immunofluorescence assays. MeHg exposure induced defects in spatial learning and memory accompanied by a decrease in number of doublecortin (DCX)-positive cells in the dentate gyrus (DG). DCX is a surrogate marker for newly generated neurons. Proliferation and differentiation of hNSCs significantly decreased in the MeHg-treated groups. MeHg attenuated microtubule-associated protein-2 (MAP-2) expression in neurons and enhanced the glial fibrillary acidic protein (GFAP)-positive cell differentiation of hNSCs, thereby inducing degenerative changes in a dose-dependent manner. Moreover, MeHg induced deficits in hippocampus-dependent spatial learning and memory during adolescence as a consequence of decreased generation of DG neurons. Our findings suggested that MeHg exposure could be a potential risk factor for psychiatric and neurodegenerative diseases. PMID:26743863

  7. Hg concentrations in fish from coastal waters of California and Western North America

    Science.gov (United States)

    Davis, Jay; Ross, John; Bezalel, Shira; Sim, Lawrence; Bonnema, Autumn; Ichikawa, Gary; Heim, Wes; Schiff, Kenneth C; Eagles-Smith, Collin A.; Ackerman, Josh

    2016-01-01

    The State of California conducted an extensive and systematic survey of mercury (Hg) in fish from the California coast in 2009 and 2010. The California survey sampled 3483 fish representing 46 species at 68 locations, and demonstrated that methylHg in fish presents a widespread exposure risk to fish consumers. Most of the locations sampled (37 of 68) had a species with an average concentration above 0.3 μg/g wet weight (ww), and 10 locations an average above 1.0 μg/g ww. The recent and robust dataset from California provided a basis for a broader examination of spatial and temporal patterns in fish Hg in coastal waters of Western North America. There is a striking lack of data in publicly accessible databases on Hg and other contaminants in coastal fish. An assessment of the raw data from these databases suggested the presence of relatively high concentrations along the California coast and in Puget Sound, and relatively low concentrations along the coasts of Alaska and Oregon, and the outer coast of Washington. The dataset suggests that Hg concentrations of public health concern can be observed at any location on the coast of Western North America where long-lived predator species are sampled. Output from a linear mixed-effects model resembled the spatial pattern observed for the raw data and suggested, based on the limited dataset, a lack of trend in fish Hg over the nearly 30-year period covered by the dataset. Expanded and continued monitoring, accompanied by rigorous data management procedures, would be of great value in characterizing methylHg exposure, and tracking changes in contamination of coastal fish in response to possible increases in atmospheric Hg emissions in Asia, climate change, and terrestrial Hg control efforts in coastal watersheds.

  8. Changing climate and sea level alter Hg mobility at Lake Tulane, Florida, U.S.

    Science.gov (United States)

    Jacobson, G L; Norton, S A; Grimm, E C; Edgar, T

    2012-11-01

    Between 45,000 cal years BP and the beginning of the Holocene, the accumulation rate for Hg in sediments of Lake Tulane, Florida ranged from ≈2 to 10 μg m(-2) yr(-1), compared with 53 μg Hg m(-2) yr(-1) in the 1985-1990 period of anthropogenic input. The locality experienced regional draw-down of the water table during the Wisconsinan glaciation, which lowered global sea level by nearly 130 m. Natural atmospheric deposition of Hg to the surrounding area resulted in long-term (ca. 100,000 years) sequestration of this atmospheric flux of Hg, primarily by adsorption in the oxic Al- and Fe-hydroxide-rich sandy subsoil. Global sea level rise during deglaciation led to a rising regional water table, flooding the oxidized soils surrounding Tulane. Iron and adsorbed Hg were mobilized by reductive dissolution and transported by groundwater flow to Lake Tulane and ultimately to the accumulating sediment. The accumulation rate of Hg (and Fe) increased rapidly about 16,000 cal years BP, peaked at nearly 60 μg Hg m(-2) yr(-1) ca. 13,000-14,000 cal years BP, declined sharply during the Younger Dryas, and then increased sharply to a second 60 μg Hg m(-2) yr(-1) peak about 5000 cal years BP. Thereafter, it declined nearly to background by 900 cal years BP. In similar geologic situations, rapid modern sea level rise will initiate this process globally, and may mobilize large accumulations of Hg and lesser amounts of As, and other redox sensitive metals to groundwater and surface water.

  9. Dissolved low-molecular weight thiol concentrations from the U.S. GEOTRACES North Atlantic Ocean zonal transect

    Science.gov (United States)

    Swarr, Gretchen J.; Kading, Tristan; Lamborg, Carl H.; Hammerschmidt, Chad R.; Bowman, Katlin L.

    2016-10-01

    Low-molecular weight thiols, including cysteine and glutathione, are biomolecules involved in a variety of metabolic pathways and act as important antioxidant and metal buffering agents. In this last capacity, they represent a potential mechanism for modulating the bioavailability and biogeochemistry of many trace elements in the ocean, particularly for chalcophilic elements (e.g., Cu, Zn, Cd, Ag and Hg). For this reason, and in the context of the international GEOTRACES program that seeks to understand the biogeochemistry of trace elements in the ocean, we measured the concentration of individual dissolved low-molecular weight thiols during the U.S. GEOTRACES North Atlantic Zonal Transect (USGNAZT). Only two thiols were identified, cysteine and glutathione, in contrast to results from the northeast subarctic Pacific Ocean, where the dipeptides glycine-cysteine and arginine-cysteine were also present and γ-glutamylcysteine was dominant. Concentrations of cysteine and glutathione in the North Atlantic Ocean were lower than in the Pacific and ranged from below detection (~0.01 nM) to 0.61 nM of cysteine and up to 1.0 nM of glutathione, with cysteine generally more abundant than glutathione. Vertical profiles of cysteine and glutathione were broadly consistent with their biological production, being more abundant in surface water and usually below detection at depths greater than about 200 m. Subsurface concentration maxima, often co-incident with the deep chlorophyll maximum, were frequently observed but not universal. We conclude that cysteine and glutathione do not make up significant portions of complexation capacity for Cu and Zn in the upper open ocean but could be important for Cd, Hg, and potentially other chalcophiles. Extremely low concentrations of cysteine and glutathione in deep water suggest that higher molecular-weight thiols are a more important ligand class for chalcophiles in that portion of the ocean.

  10. Novel methodology for the study of mercury methylation and reduction in sediments and water using 197Hg radiotracer.

    Science.gov (United States)

    Ribeiro Guevara, Sergio; Zizek, Suzana; Repinc, Urska; Pérez Catán, Soledad; Jaćimović, Radojko; Horvat, Milena

    2007-03-01

    Mercury tracers are powerful tools that can be used to study mercury transformations in environmental systems, particularly mercury methylation, demethylation and reduction in sediments and water. However, mercury transformation studies using tracers can be subject to error, especially when used to assess methylation potential. The organic mercury extracted can be as low as 0.01% of the endogenous labeled mercury, and artefacts and contamination present during methylmercury (MeHg) extraction processes can cause interference. Solvent extraction methods based on the use of either KBr/H2SO4 or HCl were evaluated in freshwater sediments using 197Hg radiotracer. Values obtained for the 197Hg tracer in the organic phase were up to 25-fold higher when HCl was used, which is due to the coextraction of 197Hg2+ into the organic phase during MeHg extraction. Evaluations of the production of MeHg gave similar results with both MeHg extraction procedures, but due to the higher Hg2+ contamination of the controls, the uncertainty in the determination was higher when HCl was used. The Hg2+ contamination of controls in the HCl extraction method showed a nonlinear correlation with the humic acid content of sediment pore water. Therefore, use of the KBr/H2SO4 method is recommended, since it is free from these interferences. 197Hg radiotracer (T1/2=2.673 d) has a production rate that is about 50 times higher than that of 203Hg (T1/2=46.595 d), the most frequently used mercury radiotracer. Hence it is possible to obtain a similar level of performance to 203Hg when it is used it in short-term experiments and produced by the irradiation of 196Hg with thermal neutrons, using mercury targets with the natural isotopic composition. However, if the 0.15% natural abundance of the 196Hg isotope is increased, the specific activity of the 197Hg tracer can be significantly improved. In the present work, 197Hg tracer was produced from mercury 51.58% enriched in the 196Hg isotope, and a 340-fold

  11. Hg Substitution Effect on Superconductivity and Crystal Structure of MgB2

    Institute of Scientific and Technical Information of China (English)

    Ya-Jing Cui; Yong-Liang Chen; Ye Yang; Yong Zhang; Cui-Hua Cheng; Yong Zhao

    2008-01-01

    Polycrystalline Mg1-xHgxB2 samples with x=0, 1%, 2.5%, 5%, 7.5%, and 10% have been synthe- sized by solid-state reaction. Different from the substitu- tion effect of Al, C, Li, etc. on crystal structure of MgB2, Hg substitution for Mg results in an increase of the lattice constant in both a and c directions. The super- conductivity of MgB2 is also suppressed by Hg substi- tution. The observed suppression of super- conductivity by Hg substitution is discussed in terms of the interband impurity scattering effect in two-band superconductors.

  12. Kinetics and mechanism of jack bean urease inhibition by Hg2+

    Directory of Open Access Journals (Sweden)

    Du Nana

    2012-12-01

    Full Text Available Abstract Background Jack bean urease (EC 3.5.1.5 is a metalloenzyme, which catalyzes the hydrolysis of urea to produce ammonia and carbon dioxide. The heavy metal ions are common inhibitors to control the rate of the enzymatic urea hydrolysis, which take the Hg2+ as the representative. Hg2+ affects the enzyme activity causing loss of the biological function of the enzyme, which threatens the survival of many microorganism and plants. However, inhibitory kinetics of urease by the low concentration Hg2+ has not been explored fully. In this study, the inhibitory effect of the low concentration Hg2+ on jack bean urease was investigated in order to elucidate the mechanism of Hg2+ inhibition. Results According to the kinetic parameters for the enzyme obtained from Lineweaver–Burk plot, it is shown that the Km is equal to 4.6±0.3 mM and Vm is equal to 29.8±1.7 μmol NH3/min mg. The results show that the inhibition of jack bean urease by Hg2+ at low concentration is a reversible reaction. Equilibrium constants have been determined for Hg2+ binding with the enzyme or the enzyme-substrate complexes (Ki =0.012 μM. The results show that the Hg2+ is a noncompetitive inhibitor. In addition, the kinetics of enzyme inhibition by the low concentration Hg2+ has been studied using the kinetic method of the substrate reaction. The results suggest that the enzyme first reversibly and quickly binds Hg2+ and then undergoes a slow reversible course to inactivation. Furthermore, the rate constant of the forward reactions (k+0 is much larger than the rate constant of the reverse reactions (k-0. By combining with the fact that the enzyme activity is almost completely lost at high concentration, the enzyme is completely inactivated when the Hg2+ concentration is high enough. Conclusions These results suggest that Hg2+ has great impacts on the urease activity and the established inhibition kinetics model is suitable.

  13. Induced superconductivity in the surface state of mercury telluride (HgTe)

    International Nuclear Information System (INIS)

    It has been recently shown that the strained epitaxial growth of bulk HgTe layers opens a band gap in the normally semi-metallic material. This means that strained HgTe meets all prerequisites of a topological insulator, i.e. surface states and an insulating bulk, which does not contribute to transport measurements. The interfaces between topological insulators and superconductors are especially interesting due to the possibility of creation and detection of majorana fermions. Our current work is focussing on investigating contacts between strained HgTe and Nb as a superconducting material. First results show proximity effect and multiple sub gap features which are discussed in detail.

  14. Solvothermal Synthesis and Characterization of HgTe Nanoplatelets Using Mercury(Ⅰ) Source

    Institute of Scientific and Technical Information of China (English)

    WU Ke-Jun; WANG Ming-Sheng; ZOU Jian-Ping; XU Gang; DING Tong-Yong; GUO Guo-Cong; HUANG Jin-Shun

    2008-01-01

    Mercury telluride (HgTe) nanoplatelets were obtained via a facile solvothermal reaction of mercury(Ⅰ) chloride and tellurium powder in ethylenediamine (en). Mercury(Ⅰ) was first applied as the mercury sources to prepare nanocrystal HgTe; moreover, the proposed mechanism for the fabrication of the sample was discussed in detail. The HgTe nanoplatelets were characterized by powder X-ray diffraction (PXRD), scanning electron microscopy (SEM),transmission electron microscopy (TEM), high-resolution transmission electron microscopy(HRTEM) and Fourier transform infrared spectroscopy (FT-IR). The absence of IR absorption may render the title nanocrystal useful as an IR transparent material in the region.

  15. A longitudinally electron-beam-pumped CdHgTe laser

    Science.gov (United States)

    Borisov, B. G.; Lavrushin, B. M.; Nasibov, A. S.; Sypchenko, M. N.; Sherman, B. L.

    1989-10-01

    Lasers have been fabricated utilizing CdHgTe/CdTe heterostructures which were grown by the liquid-phase epitaxy method. The epitaxial CdHgTe layer was the active region of the cavity and the CdTe substrate was passive. Laser action in Cd(0.65)Hg(0.35)Te was achieved at a wavelength of 1.48 micron, a temperature of 77 K, and an electron energy of 50 keV. A maximum external differential efficiency of 3.4 percent was achieved.

  16. BRIEF COMMUNICATIONS: Longitudinal electron-beam-pumped CdHgTe laser

    Science.gov (United States)

    Borisov, B. G.; Lavrushin, B. M.; Nasibov, A. S.; Sypchenko, M. N.; Sherman, B. L.

    1989-10-01

    A CdHgTe/CdTe heterostructure grown by liquid phase epitaxy was used to develop a laser. The CdHgTe epitaxial laser formed the active region whilst the CdTe substrate formed the passive part of the resonator. At an electron energy of 50 keV and a temperature of 77 K, lasing was obtained at 1.48 μm in Cd0.65Hg0.35Te. The maximum external differential efficiency was 3.4%.

  17. HgTe/CdTe heterojunctions: A lattice-matched Schottky barrier structure

    OpenAIRE

    Kuech, T. F.; McCaldin, J. O.

    1982-01-01

    HgTe-CdTe lattice-matched heterojunctions were formed by the epitaxial growth of HgTe on CdTe substrates using a low-temperature metal organic chemical vapor deposition technique. These heterojunctions combine features of the Schottky barrier structure, due to the high carrier concentrations found in the semimetallic HgTe, with the structural perfection present in a lattice-matched heterojunction. The measured Schottky barrier height varied from 0.65 to 0.92 eV depending on the details of the...

  18. Place of HgI2 energy-dispersive x-ray detectors

    International Nuclear Information System (INIS)

    After a review of solid-state conduction counters, in general, and of the history of mercuric iodide, in particular, the theory of operation of solid-state energy-dispersive HgI2 detectors is dicusssed. The main factors which limit energy resolution in solid-state compound detectors are considered, including statistical fluctuations in charge generation, the window effect, trapping, inhomogeneities in the detector material, and electronic noise. Potential applications of room-temperature HgI2 x-ray detectors are listed, and general considerations are discussed for x-ray fluorescence analysis with HgI2. Directions of current investigations are given

  19. Abundancias químicas de dos binarias de HgMn

    Science.gov (United States)

    Gonzalez, E. J.; González, J. F.; Collado, A. E.

    We present the results of the abundance analysis of two HgMn single-line binary systems: NGC 2287-106 and NGC 6025-14. The spectroscopic ob- servations have been carried out at the Complejo Astronómico el Leon-cito (CASLEO) with the REOSC spectrograph in cross-dispersion mode, cov- ering the spectral range 3800-5800 ≈. Compared to the Sun, NGC 6025-14 shows great overabundances of Hg, Mn, P, Ga and Xe, while Hg, Mn, Sr, Pt and Zr are overabundant in NGC 2287-106. FULL TEXT IN SPANISH

  20. Hg(2+) mediated quinazoline ensemble for highly selective recognition of Cysteine.

    Science.gov (United States)

    Anand, Thangaraj; Sivaraman, Gandhi; Chellappa, Duraisamy

    2014-04-01

    A fluorimetric sensor for Hg(2+) ion and Cysteine based on quinazoline platform was designed and synthesized by one step reaction and characterized by using common spectroscopic methods. Time Dependent Density Functional Theory calculations shows that probe behaves as "ON-OFF" fluorescent quenching sensor via electron transfer/heavy atom effect. Receptor was found to exhibit selective fluorescence quenching behavior over the other competitive metal ions, and also the receptor-Hg(2+) ensemble act as an efficient "OFF-ON" sensor for Cysteine. Moreover this sensor has also been successfully applied to detection of Hg(2+) in natural water samples with good recovery. PMID:24384358

  1. Additional evidence concerning the valence-band offset in HgTe/CdTe

    Science.gov (United States)

    Young, P. M.; Ehrenreich, H.

    1991-05-01

    The consistency of large values of the valence-band offset, Λ, in HgTe/CdTe superlattices with magneto-optical experiments is examined in light of data on a 90-Å HgTe/40-Å CdTe superlattice. The data are shown to be consistent with values Λ=400+/-40 meV rather than the much smaller cited values. This analysis, when considered with photoemission experiments, leaves intact the conclusion that HgTe/CdTe superlattices are best explained by a large offset.

  2. Fluorescent Gold Nanoprobes for the Sensitive and Selective Detection for Hg2+

    Directory of Open Access Journals (Sweden)

    Chai Fang

    2010-01-01

    Full Text Available Abstract A simple, cost-effective yet rapid and sensitive sensor for on-site and real-time Hg2+ detection based on bovine serum albumin functionalized fluorescent gold nanoparticles as novel and environmentally friendly fluorescent probes was developed. Using this probe, aqueous Hg2+ can be detected at 0.1 nM in a facile way based on fluorescence quenching. This probe was also applied to determine the Hg2+ in the lake samples, and the results demonstrate low interference and high sensitivity.

  3. Mechanism of HgCl2 cytotoxicity in cultured mammalian cells.

    Science.gov (United States)

    Cantoni, O; Christie, N T; Swann, A; Drath, D B; Costa, M

    1984-09-01

    Treatment of intact Chinese hamster ovary cells with HgCl2 produced a rapid, concentration-dependent induction of DNA single-strand breaks (SSB) as revealed by alkaline elution analysis. Direct addition of HgCl2 to cell lysates did not result in DNA strand breaks. HgCl2 treatment of cells also caused a rapid leakage of superoxide radicals that were detected in their media by measurement of the reduction of exogenously added cytochrome c. There was a linear relationship between the production of radicals and the induction of DNA strand breaks, and there were also excellent temporal correlations in these parameters. Addition of oxygen radical scavengers, such as the enzymes superoxide dismutase and catalase, to the extracellular media significantly reduced the extent of DNA damage caused by HgCl2 without a similar attenuation of its uptake into cells, as did the autoclaved enzymes. Similarly, addition of radical scavengers such as glycerol or ascorbate inhibited the DNA damage but also reduced the uptake of the metal by almost the same degree. Thus, because of secondary effects on uptake of the metal, the radical scavenger experiments could not address the importance of oxygen radicals in the DNA damage caused by HgCl2. SSB were enhanced when cells were treated with HgCl2 and diethylmaleate or diethyldithiocarbamate, agents that deplete cellular reduced glutathione or inhibit the intracellular activity of superoxide dismutase, respectively. Thus, DNA damage in cells rendered sensitive to radicals was greater when these cultures were subsequently treated with HgCl2. The binding of 203HgCl2 to the DNA of intact Chinese hamster ovary cells was also studied. These studies were made possible by the relatively high stability of Hg(II) interaction with DNA and by utilizing a gentle method of DNA isolation that minimized redistribution of intracellular Hg(II) complexes after cells were lysed. The amount of Hg(II) bound to DNA varied from approximately 7 to 35 Hg atoms per 10

  4. Lattice dynamical properties of MnTe, HgTe and their mixed semiconductor MnHg1−Te

    Indian Academy of Sciences (India)

    A K Kushwaha

    2015-12-01

    In the present paper, the phonon dispersion relations, phonon density of states and Debye characteristics of mixed semiconductor MnHg1−Te and the end members MnTe and HgTe using three-body shell model were studied. The model involves 11 disposable parameters and incorporates the effect of the short-range repulsive interactions up to and including the second nearest neighbours, in addition to the long-range Coulombic interactions in the framework of the rigid-shell model with both the ions polarizable. The comparisons of the theoretical results with the available experimental results were in good agreement.

  5. Microscopic studies of radioactive Hg implanted in YBa$_{2}$Cu$_{3}$O$_{6+x}$ superconducting thin films

    CERN Document Server

    Amaral, V S; Lourenço, C; Marques, J G; Mendes, J A; Baptista, M A; Araújo, J P; Moreira, J M; Sousa, J B; Alves, E; Da Silva, M F A; Soares, J C

    1998-01-01

    YBa$_{2}$Cu$_{3}$O$_{6+x}$ (YBCO) superconducting thin films implanted with low doses of radioactive $^{197m}$Hg and $^{199m}$Hg isotopes were studied with a combination of nuclear and non-nuclear characterization techniques. We show that after implantation Hg lies on an unique site in the YBCO lattice and the critical temperature increases slightly with the increase of the $^{197}$Au concentration from the nuclear transmutation of $^{197}$Hg.

  6. Assessing element-specific patterns of bioaccumulation across New England lakes

    International Nuclear Information System (INIS)

    Little is known about differences among trace elements in patterns of bioaccumulation in freshwater food webs. Our goal was to identify patterns in bioaccumulation of different elements that are large and consistent enough to discern despite variation across lakes. We measured methylmercury (MeHg) and trace element (As, Cd, Hg, Pb, and Zn) concentrations in food web components of seven New England lakes on 3–5 dates per lake, and contrasted patterns of bioaccumulation across lakes, metals and seasons. In each lake, trace element concentrations were compared across trophic levels, including three size fractions of zooplankton, planktivorous fish, and piscivorous fish. The trophic position of each food web component was estimated from N isotope analysis. Trace element concentrations varied widely among taxa, lakes and sampling dates. Yet, we identified four consistent patterns of bioaccumulation that were consistent across lakes: (1) MeHg concentration increased (i.e., was biomagnified) and Pb concentration decreased (i.e., was biodiminished) with increased trophic position. (2) Zinc concentration (as with MeHg) was higher in fish than in zooplankton, but overall variation in Zn concentration (unlike MeHg) was low. (3) Arsenic and Cd concentrations (as with Pb) were lower in fish than in zooplankton, but (unlike Pb) were not significantly correlated with trophic position within zooplankton or fish groups. (4) Average summer concentrations of As, Pb, Hg, and MeHg in zooplankton significantly predicted their concentrations in either planktivorous or piscivorous fish. Our secondary goal was to review sampling approaches in forty-five published studies to determine the extent to which current sampling programs facilitate cross-lake and cross-study comparisons of bioaccumulation. We found that studies include different components of the food web and sample too infrequently to enable strong cross-lake and cross-study comparisons. We discuss sampling strategies that would

  7. Electric dipole moments of superheavy elements: A case study on copernicium

    Science.gov (United States)

    RadžiÅ«tÄ--, Laima; Gaigalas, Gediminas; Jönsson, Per; Bieroń, Jacek

    2016-06-01

    The multiconfiguration Dirac-Hartree-Fock method was employed to calculate the atomic electric dipole moments (EDMs) of the superheavy element copernicium (Cn, Z =112 ). The EDM enhancement factors of Cn, calculated here, are about one order of magnitude larger than those of Hg. The exponential dependence of the enhancement factors on the atomic number Z along group 12 of the periodic table was derived from the EDMs of the entire homologous series, Zn, Cd, Hg, Cn, and Uhb. These results show that superheavy elements with sufficiently long half-lives are potential candidates for EDM searches.

  8. Assessing element-specific patterns of bioaccumulation across New England lakes

    Energy Technology Data Exchange (ETDEWEB)

    Ward, Darren M.; Mayes, Brandon; Sturup, Stefan; Folt, Carol L.; Chen, Celia Y., E-mail: celia.chen@dartmouth.edu

    2012-04-01

    Little is known about differences among trace elements in patterns of bioaccumulation in freshwater food webs. Our goal was to identify patterns in bioaccumulation of different elements that are large and consistent enough to discern despite variation across lakes. We measured methylmercury (MeHg) and trace element (As, Cd, Hg, Pb, and Zn) concentrations in food web components of seven New England lakes on 3-5 dates per lake, and contrasted patterns of bioaccumulation across lakes, metals and seasons. In each lake, trace element concentrations were compared across trophic levels, including three size fractions of zooplankton, planktivorous fish, and piscivorous fish. The trophic position of each food web component was estimated from N isotope analysis. Trace element concentrations varied widely among taxa, lakes and sampling dates. Yet, we identified four consistent patterns of bioaccumulation that were consistent across lakes: (1) MeHg concentration increased (i.e., was biomagnified) and Pb concentration decreased (i.e., was biodiminished) with increased trophic position. (2) Zinc concentration (as with MeHg) was higher in fish than in zooplankton, but overall variation in Zn concentration (unlike MeHg) was low. (3) Arsenic and Cd concentrations (as with Pb) were lower in fish than in zooplankton, but (unlike Pb) were not significantly correlated with trophic position within zooplankton or fish groups. (4) Average summer concentrations of As, Pb, Hg, and MeHg in zooplankton significantly predicted their concentrations in either planktivorous or piscivorous fish. Our secondary goal was to review sampling approaches in forty-five published studies to determine the extent to which current sampling programs facilitate cross-lake and cross-study comparisons of bioaccumulation. We found that studies include different components of the food web and sample too infrequently to enable strong cross-lake and cross-study comparisons. We discuss sampling strategies that would

  9. 40 CFR 75.82 - Monitoring of Hg mass emissions and heat input at common and multiple stacks.

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 16 2010-07-01 2010-07-01 false Monitoring of Hg mass emissions and... PROTECTION AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) CONTINUOUS EMISSION MONITORING Hg Mass Emission Provisions § 75.82 Monitoring of Hg mass emissions and heat input at common and multiple stacks. (a)...

  10. 40 CFR 75.81 - Monitoring of Hg mass emissions and heat input at the unit level.

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 16 2010-07-01 2010-07-01 false Monitoring of Hg mass emissions and... AGENCY (CONTINUED) AIR PROGRAMS (CONTINUED) CONTINUOUS EMISSION MONITORING Hg Mass Emission Provisions § 75.81 Monitoring of Hg mass emissions and heat input at the unit level. The owner or operator of...

  11. The platinum group elements and gold: analysis by radiochemical and instrumental neutron activation analysis and relevance to geological exploration and related problems

    Energy Technology Data Exchange (ETDEWEB)

    Reeves, S.; Plimer, I. R. [Melbourne Univ., Parkville, VIC (Australia). School of Physics

    1996-12-31

    This paper presents an overview of research conducted with the support of the Australian Institute of Nuclear Science and Engineering, at the University of Melbourne, School of Earth Sciences, Radiochemical Neutron Activation Laboratory. The primary objective of this research is to realize the high potential of the platinum group elements (PGE) and gold to the solution of petrogenetic problems, the study of magma generation and magmatic processes in mafic/ultramafic rock suites, as tracers in hydrothermal ore formation. The PGEs (Os, Ru, Ir, Pt, Pd and Rh) are among the least abundant of all elements on earth with unique properties such as high melting points, high electrical and thermal conductivity, high density, strength and toughness as alloys. They exhibit both siderophile and chalcophile characteristics and are valuable tools in providing information about magmatic processes, in particular S-saturation, as well as crystal fractionation trends. Two distinct groups of PGEs are discerned; the IPGEs (Ru, Os, Ir) and the PPGEs (Pt, Pd, Rh, Au) on the basis of their behaviour during fractionation processes. Using chondrite normalized PGE patterns it is possible to distinguish between sulphides that segregated from primitive magmas, such as komatiites, and sulphides which segregated from more fractionated magmas, such as tholeiites. It is critical to the understanding of these processes to be able to analyse key elements, such as the PGE and gold, in the parts per billion to parts per trillion range. Platinum group elements and Au were determined by radiochemical neutron activation analysis using a modified NiS fire-assay preconcentration technique, adapted from procedures first used by Robert, R.V. D. and van Wyk, E. (1975) . Detection limits are generally 0.005-0.01 ppb (Au and Ir), 0.1-0.2 ppb (Pd and Pt), and 0.1-0.5 ppb for Ru. 9 refs.

  12. Toxic and essential elements changed in black-legged kittiwakes (Rissa tridactyla) during their stay in an Arctic breeding area.

    Science.gov (United States)

    Overjordet, Ida Beathe; Kongsrud, Magnus Brunvoll; Gabrielsen, Geir Wing; Berg, Torunn; Ruus, Anders; Evenset, Anita; Borgå, Katrine; Christensen, Guttorm; Jenssen, Bjørn Munro

    2015-01-01

    Seasonal fluctuations in mercury (Hg), cadmium (Cd), zinc (Zn), copper (Cu) and selenium (Se) concentrations were studied in black-legged kittiwakes (Rissa tridactyla) from Kongsfjorden, Svalbard (79°57'N, 12°12'E). Element concentrations were determined in muscle and liver tissue in kittiwakes collected in May, July and October 2007. Stable isotopes of carbon (δ(13)C) and nitrogen (δ(15)N) were analysed in muscle tissue to calculate trophic position (TP) and examine the possible influence of carbon source on element accumulation. Metallothionein (MT) concentrations in liver, as well as Hg and Cd concentration in size-fractionated liver supernatant were determined to evaluate the association between elements and MT. Mercury concentrations declined from May through July to October in both tissues, while concentrations of Cd were similar in May and July and lower in October. A decline in TP between May and July, indicating a shift from fish-based diet towards an invertebrate-based diet explains the declining Hg concentration. The low Hg and Cd concentrations in October may be a result of an increased elimination, probably related to moulting. Selenium decreased in the same manner as Hg in liver and muscle, possibly related to the formation of Se-Hg complexes. Zinc and Cu did not fluctuate in muscle tissue, whereas hepatic Zn concentrations where highest in May. Hepatic Zn concentrations were higher in females compared to males in May, possibly related to egg production. Hepatic MT concentrations were lower in October compared to July, following the same trend as Hg and Cd. Cadmium was predominantly bound to the MT fraction of proteins in liver tissue, whereas Hg was associated with the larger proteins, indicating that MT was not sequestering Hg in the kittiwakes. PMID:25300019

  13. 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

    Pollution from heavy metals has increased in recent decades and has become an important concern for environmental agencies. Arsenic, cadmium, copper, mercury and lead are among the trace elements that have the greatest impact and carry the highest risk to human health. Electrothermal atomic absorption spectrometry (ETAAS) has long been used for trace element analyses and over the past few years, the main constraints of atomic absorption spectrometry (AAS) methods, namely matrix interferences that provoked high background absorption and interferences, have been reduced. The use of new, more efficient modifiers and in situ trapping methods for stabilization and pre-concentration of these analytes, progress in control of atomization temperatures, new designs of atomizers and advances in methods to correct background spectral interferences have permitted an improvement in sensitivity, an increase in detection power, reduction in sample manipulation, and increase in the reproducibility of the results. These advances have enhanced the utility of Electrothermal atomic absorption spectrometry (ETAAS) for trace element determination at mug L{sup -1} levels, especially in difficult matrices, giving rise to greater reproducibility, lower economic cost and ease of sample pre-treatment compared to other methods. Moreover, the recent introduction of high resolution continuum source Electrothermal atomic absorption spectrometry (HR-CS-ETAAS) has facilitated direct solid sampling, reducing background noise and opening the possibility of achieving even more rapid quantitation of some elements. The incorporation of flow injection analysis (FIA) systems for automation of sample pre-treatment, as well as chemical vapor generation renders (ETAAS) into a feasible option for detection of As and Hg in environmental and food control studies wherein large numbers of samples can be rapidly analyzed. A relatively inexpensive approach with low sample consumption provide additional advantages

  14. Elemental mercury in the atmosphere of a tropical Amazonian forest (French Guiana)

    Energy Technology Data Exchange (ETDEWEB)

    Amouroux, D.; Wasserman, J.C.Tessier, E.; Donard, O.F.X. [Univ. de Pau et des Pays de l`Adour, Pau (France). Lab. de Chimie Analytique Bio-Inorganique et Environnement

    1999-09-01

    Gaseous atmospheric mercury was investigated at two sites of a tropical Amazonian forest (French Guiana) in the Petit Inini River basin and the Petit Saut Lake in June, 1998. Gaseous atmospheric mercury was identified as elemental mercury (Hg{sup 0}). Diurnal variation of atmospheric Hg{sup 0} in both studied aquatic environments were significantly correlated with air temperature and anticorrelated with relative humidity. Average Hg{sup 0} concentrations were higher above the Petit Inini River that the Petit Saut Lake. Background Hg{sup 0} concentrations in the Petit Inini River basin were higher than those observed in remote environments. These data suggest that gold mining activity (i.e., Petit Inini River basin) may influence mercury mobilization in tropical forest ecosystems and that atmospheric transfer is a major pathway for mercury cycling in these environments.

  15. Trace elements in striped dolphins (Stenella coeruleoalba) from the Eastern Mediterranean: A 10-years perspective.

    Science.gov (United States)

    Shoham-Frider, Efrat; Goffman, Oz; Harlavan, Yehudit; Kress, Nurit; Morick, Danny; Roditi-Elasar, Mia; Shefer, Edna; Kerem, Dan

    2016-08-15

    Concentrations of Hg, Se, Cd, Cu, Zn, Fe, Mn and As, in kidney, liver, muscle and blubber from 7 specimens of Stenella coeruleoalba, stranded along the Israeli Mediterranean coast (IMC) from 2006 to 2011 (2011-series) were determined and compared to previous data on S. coeruleoalba from the IMC (2001-series). No differences were observed in essential and toxic elements concentrations, between the two series, except for hepatic Mn which was higher in the latter. Hg/Se molar ratios in blubber, kidney and liver increased linearly with log Hg concentrations, while muscle was more heterogenic in this respect. Means (±SD) of hepatic Hg concentrations (134±89 and 181±200mgkg(-1), from the 2011 and 2001 series, respectively) were similar to that found in 2007-2009 specimens from Spain, possibly reflecting the relatively high natural background levels of mercury in the Mediterranean Sea. PMID:27210566

  16. Novel Effective Catalyst for Elemental Mercury Removal from Coal-Fired Flue Gas and the Mechanism Investigation.

    Science.gov (United States)

    Chen, Wanmiao; Pei, Yang; Huang, Wenjun; Qu, Zan; Hu, Xiaofang; Yan, Naiqiang

    2016-03-01

    Mercury pollution from coal-fired power plants has drawn attention worldwide. To achieve efficient catalytic oxidation of Hg(0) at both high and low temperatures, we prepared and tested novel IrO2 modified Ce-Zr solid solution catalysts under various conditions. It was found that the IrO2/Ce0.6Zr0.4O2 catalyst, which was prepared using the polyvinylpyrrolidone-assisted sol-gel method, displayed significantly higher catalytic activity for Hg(0) oxidation. The mechanism of Hg(0) removal over IrO2/Ce0.6Zr0.4O2 was studied using various methods, and the Hg(0) oxidation reaction was found to follow two possible pathways. For the new chemisorption-regeneration mechanism proposed in this study, the adsorbed Hg(0) was first oxidized with surface chemisorbed oxygen species to form HgO; the HgO could desorb from the surface of catalysts by itself or react with adsorbed HCl to be release in the form of gaseous HgCl2. O2 is indispensable for the chemisorption process, and the doping of IrO2 could facilitate the chemisorption process. In addition, the Deacon reaction mechanism was also feasible for Hg(0) oxidation: this reaction would involve first oxidizing the adsorbed HCl to active Cl species, after which the Hg(0) could react with Cl to form HgCl2. Additionally, doping IrO2 could significantly improve the Cl yield process. In summary, the novel IrO2 modified catalyst displayed excellent catalytic activity for elemental mercury oxidation, and the proposed reaction mechanisms were determined reasonably. PMID:26815147

  17. Atmospheric gaseous elemental mercury (GEM concentrations and mercury depositions at a high-altitude mountain peak in south China

    Directory of Open Access Journals (Sweden)

    X. W. Fu

    2010-03-01

    Full Text Available China is regarded as the largest contributor of mercury (Hg to the global atmospheric Hg budget. However, concentration levels and depositions of atmospheric Hg in China are poorly known. Continuous measurements of atmospheric gaseous elemental mercury (GEM were carried out from May 2008 to May 2009 at the summit of Mt. Leigong in south China. Simultaneously, deposition fluxes of THg and MeHg in precipitation, throughfall and litterfall were also studied. Atmospheric GEM concentrations averaged 2.80±1.51 ng m−3, which was highly elevated compared to global background values but much lower than semi-rural and industrial/urban areas in China. Sources identification indicates that both regional industrial emissions and long range transport of Hg from central, south and southwest China were corresponded to the elevated GEM level. Seasonal and diurnal variations of GEM were observed, which reflected variations in source intensity, deposition processes and meteorological factors. Precipitation and throughfall deposition fluxes of THg and MeHg in Mt. Leigong were comparable or lower compared to those reported in Europe and North America, whereas litterfall deposition fluxes of THg and MeHg were higher compared to Europe and North America. This highlights the importance of vegetation to Hg atmospheric cycling. In th remote forest ecosystem of China, deposition of GEM via uptake of foliage followed by litterfall was very important for the depletion of atmospheric Hg. Elevated GEM level in ambient air may accelerate the foliar uptake of Hg through air which may partly explain the elevated litterfall deposition fluxes of Hg observed in Mt. Leigong.

  18. Performance evaluation of non-thermal plasma injection for elemental mercury oxidation in a simulated flue gas

    International Nuclear Information System (INIS)

    Graphical abstract: - Highlights: • The use of non-thermal plasma injection approach to oxidize Hg0 in simulated flue gas at 110 °C was studied. • A high Hg0 oxidation efficiency was observed in the mixed flue gas that included O2, H2O, SO2, NO and HCl. • Chemical and physical processes (e.g., ozone, N2 metastable states and UV-light) contributed to Hg0 oxidation. • Mercury species mainly existed in the form of HgO(s) adhering to the suspended aerosols in the gas-phase. - Abstract: The use of non-thermal plasma (NTP) injection approach to oxidize elemental mercury (Hg0) in simulated flue gas at 110 °C was studied, where a surface discharge plasma reactor (SDPR) inserted in the simulated flue duct was used to generate and inject active species into the flue gas. Approximately 81% of the Hg0 was oxidized and 20.5 μg kJ−1 of energy yield was obtained at a rate of 3.9 J L−1. A maximal Hg0 oxidation efficiency was found with a change in the NTP injection air flow rate. A high Hg0 oxidation efficiency was observed in the mixed flue gas that included O2, H2O, SO2, NO and HCl. Chemical and physical processes (e.g., ozone, N2 metastable states and UV-light) were found to contribute to Hg0 oxidation, with ozone playing a dominant role. The deposited mercury species on the internal surface of the flue duct was analyzed using X-ray photoelectron spectroscopy (XPS) and electronic probe microanalysis (EPMA), and the deposit was identified as HgO. The mercury species is thought to primarily exist in the form of HgO(s) by adhering to the suspended aerosols in the gas-phase

  19. Effects of flue gas components on removal of elemental mercury over Ce-MnOx/Ti-PILCs.

    Science.gov (United States)

    He, Chuan; Shen, Boxiong; Li, Fukuan

    2016-03-01

    The adsorption and oxidation of elemental mercury (Hg(0)) under various flue gas components were investigated over a series of Ce-MnOx/Ti-PILC catalysts, which were synthesized by an impregnation method. To discuss the mechanism, the catalysts were characterized by various techniques such as N2 adsorption-desorption, scanning electron microscope (SEM), X-ray diffraction (XRD), Fourier transform infrared (FTIR) analysis and X-ray photoelectron spectroscopy (XPS). The results indicated that the presence of 500 ppm SO2 in the flue gas significantly restrained the Hg(0) adsorption and oxidation over 6%Ce-6%MnOx/Ti-PILC due to the formation of SO4(2-) species. Hg(0) could be oxidized to HgCl2 in the presence of HCl, because the Deacon process occurred. NO would react with active oxygen to form NO2-containing species, which facilitated Hg(0) oxidation. While the presence of NO limited the Hg(0) adsorption on 6%Ce-6%MnOx/Ti-PILC due to the competitive adsorption of NO with Hg(0). The addition of NH3 in the flue gas significantly restrained Hg(0) adsorption and oxidation, because the formed NH4(+) species covered the active adsorption sites on the surfaces, and further limited Hg(0) oxidation. However, when NO and NH3 were simultaneously added into the flue gas, the Hg(0) oxidation efficiency of 6%Ce-6%MnOx/Ti-PILC exhibited a relatively high value (72%) at 250°C, which indicated the practicability to use Ce-MnOx/Ti-PILC for Hg(0) removal under SCR conditions. PMID:26546699

  20. Deformation properties of the neutron-deficient ODD-A Pt and Hg nuclei

    Energy Technology Data Exchange (ETDEWEB)

    Sauvage, J.; Libert, J.; Roussiere, B.; Verney, D.; Ibrahim, F.; Le Blanc, F.; Oms, J. [Paris-11 Univ., 91 - Orsay (France). Inst. de Physique Nucleaire; Cabaret, L.; Pinard, J. [Laboratoire Aime Cotton, 91 - Orsay (France); Crawford, J.E.; Lee, J.K.P. [Physics Dept., Mc Gill University, Montreal (Canada); Genevey, J. [Institut des Sciences Nucleaires, IN2P3-CNRS, 38 - Grenoble (France); Huber, G. [Institut fur Physik der Universitat Mainz (Germany)

    2000-07-01

    Nuclear and atomic spectroscopy measurements have provided a great number of data on the neutron-deficient Pt and Hg nuclei. The odd-A Pt and Hg with A<186 have a prolate shape, the even-even isotopes have a triaxial shape while the nuclear shape of the odd-A Pt and Hg with A>186 is still an open question. The energy of the low-lying levels and the nuclear moments have been calculated in the framework of a semi-microscopic axial-rotor + I quasiparticle coupling model. The predictions are compared with the experimental data and discussed. The results strongly suggest a prolate shape for the negative-parity low-lying states of the odd-A {sup 187-191}Pt and {sup 187-193}Hg isotopes. (authors)

  1. Ultra-low Noise, High Bandwidth, 1550nm HgCdTe APD Project

    Data.gov (United States)

    National Aeronautics and Space Administration — Voxtel Inc. proposes to optimize the design of a large area, 1.55?m sensitive HgCdTe avalanche photodiode (APD) that achieves high gain with nearly no excess noise....

  2. Large format MBE HgCdTe on silicon detector development for astronomy

    Science.gov (United States)

    Hanold, Brandon J.; Figer, Donald F.; Lee, Joong; Kolb, Kimberly; Marcuson, Iain; Corrales, Elizabeth; Getty, Jonathan; Mears, Lynn

    2015-08-01

    The Center for Detectors at Rochester Institute of Technology and Raytheon Vision Systems (RVS) are leveraging RVS capabilities to produce large format, short-wave infrared HgCdTe focal plane arrays on silicon (Si) substrate wafers. Molecular beam epitaxial (MBE) grown HgCdTe on Si can reduce detector fabrication costs dramatically, while keeping performance competitive with HgCdTe grown on CdZnTe. Reduction in detector costs will alleviate a dominant expense for observational astrophysics telescopes. This paper presents the characterization of 2.5μm cutoff MBE HgCdTe/Si detectors including pre- and post-thinning performance. Detector characteristics presented include dark current, read noise, spectral response, persistence, linearity, crosstalk probability, and analysis of material defects.

  3. The direct determination of HgS by thermal desorption coupled with atomic absorption spectrometry

    Science.gov (United States)

    Coufalík, Pavel; Zvěřina, Ondřej; Komárek, Josef

    2016-04-01

    This research was aimed at the direct determination of HgS in environmental samples by means of thermal desorption coupled with atomic absorption spectrometry. Operating parameters of the apparatus used for thermal desorption (including a prototype desorption unit) are described in this work, as well as the procedure for measuring mercury release curves together with an evaluation of the analytical signal including two methods of peak integration. The results of thermal desorption were compared with HgS contents obtained by sequential extraction. The limits of quantification of the proposed method for the selective determination of the black and red forms of HgS were 4 μg kg- 1 and 5 μg kg- 1, respectively. The limit of quantification of red HgS in soils was 35 μg kg- 1. The developed analytical procedure was applied to soil and sediment samples from historical mining areas.

  4. HgI2 detectors for Pu contamination monitoring and radiological protection measurements

    International Nuclear Information System (INIS)

    HgI2 detectors developed from solution-grown crystals show good-detection properties (resolution, efficiency, stability) for X-rays and low-energy gamma rays (EL. Two examples of devices based on these HgI2 detectors are shown: (1) A compact probe for Pu detection in wounds which gives also information on the depth of the contamination, and (2) an array of 16x1 cm2 HgI2 detectors for Pu contamination of soil or wet surfaces where alpha detection is not valid. A tentative use of HgI2 detectors as compact ionization chambers working in the current mode is also described. (orig.)

  5. The extent of mercury (Hg) exposure among Saudi mothers and their respective infants.

    Science.gov (United States)

    Al-Saleh, Iman; Abduljabbar, Mai; Al-Rouqi, Reem; Eltabache, Chafica; Al-Rajudi, Tahreer; Elkhatib, Rola; Nester, Michael

    2015-11-01

    A total of 1016 healthy Saudi mothers and their respective infants (aged 3-12 months) were recruited from 57 Primary Health Care Centers (PHCCs) in Riyadh, Saudi Arabia, to evaluate the extent of mercury (Hg) exposure and predict its sources in the healthy Saudi population. Total Hg levels were measured in maternal urine, breast milk, blood, and hair and in the infants' urine and hair. Only 1.9% of the mothers had urinary Hg (UHg)>10 μg/l, the limit for asymptomatic adults recommended by the World Health Organization, but the median (0.99 μg/l) was higher than in other countries. Also, 49.3% of the mothers had UHg>1 μg/l, the German reference value for adults. Median infant UHg was 0.729 μg/l, and 77 and 93 % of the infants had levels higher than 0.4 and 0.1 μg/l, the reference values of the Centers for Disease Control and Prevention and for Germany, respectively. The median Hg level in breast milk was 0.884 μg/l. Even though 43.2% of the milk samples were above the background level for Hg in human milk (1 μg/l), our results were lower than those reported from other countries. Median maternal total Hg in blood was 0.637 μg/l, and only 0.4 and 6.9% of samples were higher than the Hg reference levels of 5.8 μg/l of the Environmental Protection Agency (EPA) and of 2 μg/l for Germany, respectively. Total Hg levels in hair (HHg) varied widely among mothers and infants, but only 3.9% of the mothers and 2.8% of the infants had HHg>1 μg/g (the EPA reference level). Median HHg values were 0.117 μg/g dry weight in mothers and 0.1 μg/g dry weight in infants; both were lower than in other countries. The Hg levels in mothers and their respective infants were relatively low, but our results were consistent with other studies indicating that dental amalgam fillings and fish consumption were the main predictors of maternal Hg exposure. Among the several biomarkers of Hg exposure, Hg levels in maternal hair and urine were the strongest predictors of infant exposure

  6. Results of Hg speciation testing on tanks 30, 32, and 37 surface samples

    Energy Technology Data Exchange (ETDEWEB)

    Bannochie, C. J. [Savannah River Site (SRS), Aiken, SC (United States)

    2015-11-11

    The Savannah River National Laboratory (SRNL) was tasked with preparing and shipping samples for Hg speciation by Eurofins Frontier Global Sciences, Inc. in Seattle, WA on behalf of the Savannah River Remediation (SRR) Mercury Task Team.

  7. Theoretical Calculations of Refractive Properties for Hg3Te2Cl2 Crystals.

    Science.gov (United States)

    Bokotey, O V

    2016-12-01

    This paper reviews the optical properties, such as refractive index, optical dielectric constant, and reflection coefficient of the Hg3Te2Cl2 crystals. The applications of the Hg3X2Y2 crystals as electronic, optical, and optoelectronic devices are very much determined by the nature and magnitude of these fundamental material properties. The origin of chemical bonding in the crystals is very important for definition of the physical and chemical properties. The main structural feature of the Hg3X2Y2 crystals is the presence of covalent pyramids [XHg3] and linear X-Hg-X groups. Optical properties are calculated according to the model proposed by Harrison. The refractive index in the spectral region far from the absorption edge is determined within the generalized single-oscillator model. The calculated results are found to be in good agreement with experimental data. PMID:27184964

  8. Theoretical Calculations of Refractive Properties for Hg3Te2Cl2 Crystals

    Science.gov (United States)

    Bokotey, O. V.

    2016-05-01

    This paper reviews the optical properties, such as refractive index, optical dielectric constant, and reflection coefficient of the Hg3Te2Cl2 crystals. The applications of the Hg3X2Y2 crystals as electronic, optical, and optoelectronic devices are very much determined by the nature and magnitude of these fundamental material properties. The origin of chemical bonding in the crystals is very important for definition of the physical and chemical properties. The main structural feature of the Hg3X2Y2 crystals is the presence of covalent pyramids [XHg3] and linear X-Hg-X groups. Optical properties are calculated according to the model proposed by Harrison. The refractive index in the spectral region far from the absorption edge is determined within the generalized single-oscillator model. The calculated results are found to be in good agreement with experimental data.

  9. Doping behavior of iodine in Hg/0.8/Cd/0.2/Te

    Science.gov (United States)

    Vydyanath, H. R.; Kroger, F. A.

    1982-01-01

    The defect state prevailing in iodine doped single-crystal samples of Hg0.8Cd0.2Te, annealed at 450-600 C in Hg vapor, has been deduced from Hall effect measurements on samples cooled to 77 K from the annealing temperature. Results are found to be similar to those previously obtained for iodine doped CdS, i.e. iodine acts as a single donor occupying Te lattice sites with a fraction paired with the native acceptor defects. The concentration of iodine on tellurium lattice sites increases with the partial pressure of Hg, whereas that of the pair species increases as the partial pressure of Hg decreases.

  10. Evidence for Half-Metallicity in n-type HgCr2Se4.

    Science.gov (United States)

    Guan, Tong; Lin, Chaojing; Yang, Chongli; Shi, Youguo; Ren, Cong; Li, Yongqing; Weng, Hongming; Dai, Xi; Fang, Zhong; Yan, Shishen; Xiong, Peng

    2015-08-21

    High quality HgCr2Se4 single crystals have been investigated by magnetization, electron transport, and Andreev reflection spectroscopy. In the ferromagnetic ground state, the saturation magnetic moment of each unit cell corresponds to an integer number of electron spins (3  μB/Cr3+), and the Hall effect measurements suggest n-type charge carriers. Spin polarizations as high as 97% were obtained from fits of the differential conductance spectra of HgCr2Se4/Pb junctions with the modified Blonder-Tinkham-Klapwijk theory. The temperature and bias-voltage dependencies of the subgap conductance are consistent with recent theoretical calculations based on spin active scatterings at a superconductor-half-metal interface. Our results suggest that n-HgCr2Se4 is a half-metal, in agreement with theoretical calculations that also predict undoped HgCr2Se4 is a magnetic Weyl semimetal. PMID:26340201

  11. Point defects with lattice distortion in CdTe and HgCdTe

    Energy Technology Data Exchange (ETDEWEB)

    Schick, J.T.; Morgan-Pond, C.G. (Department of Physics Astronomy, Wayne State University, Detroit, Michigan 48202 (US))

    1990-03-01

    Results of self-consistent, tight-binding supercell calculations of electronic defect levels and relaxation about defects for As, Sb, and Te interstitials in CdTe and for the Hg vacancy in HgTe are presented. Trends in the localized defect levels and the relaxation of the lattice seen for these defects and for Cd, Hg, and In interstitials, from previous calculations, are discussed. Te interstitials are found to have the largest lattice relaxation of these interstitials in their preferred tetrahedral positions. This may help explain the tendency for excess Te to condense into second-phase inclusions. It is also suggested that a strain-mediated interaction between Te interstitials and cation vacancies may promote the creation of Te antisites in Te-rich HgCdTe.

  12. HgO-added YBa2Cu3O7- superconductors

    Indian Academy of Sciences (India)

    Mangalesh Dixit; Shovit Bhattacharya; Rajneesh Mohan; Kiran Singh; P S R Krishna; Vilas Shelke; N K Gaur; R K Singh

    2004-08-01

    The HgO-added YBa2Cu3O7- (YBCO) superconductor has been studied for its structural and superconducting properties. Polycrystalline YBCO samples were synthesized through solid-state reaction method by adding HgO in different concentrations without using oxygen annealing. All the samples showed a sharp superconducting transition temperature around 90 K. The X-ray diffraction patterns of all the samples revealed monophasic Y-123 nature. The structural studies were carried out by neutron scattering and Rietveld analysis. The neutron scattering revealed that Hg is not incorporated in the Y-123 system and has shown optimum oxygen concentration. The significant role played by the HgO is to provide oxygen ambient through its decomposition, thus changing the oxygen balance in favour of high Cu-valence state.

  13. Estimation of Thickness and Cadmium Composition Distributions in HgCdTe Focal Plane Arrays

    Science.gov (United States)

    Mouzali, S.; Lefebvre, S.; Rommeluère, S.; Ferrec, Y.; Primot, J.

    2016-09-01

    Mercury cadmium telluride (HgCdTe) is one of the most commonly used material systems for infrared detection. The performance of infrared focal-plane arrays (IRFPAs) based on this material is limited by several noise sources. In this paper, we focus on the fixed pattern noise, which is related to disparities between the spectral responses of pixels. In our previous work, we showed that spectral nonuniformities in a HgCdTe IRFPA were caused by inhomogeneities of thickness and cadmium composition in the HgCdTe layer, using an optical description of the pixel structure. We propose to use this bidimensional dependence combined with experimental spectral responses to estimate disparities of thickness and cadmium composition in a specific HgCdTe-based IRFPA. The estimation methods and the resulting maps are presented, highlighting the accuracy of this nondestructive method.

  14. Characteristics of HgCdTe epilayer grown by LPE using horizontal slider

    Indian Academy of Sciences (India)

    J K Radhakrishnan; S Sitharaman; S C Gupta

    2002-11-01

    The characteristics of HgCdTe epilayers grown in a modified horizontal slider system, are reported here. The surface morphology of the grown layers, their IR transmission characteristics, depth and lateral compositional uniformity, structural and electrical characteristics are discussed.

  15. Effect of pH and temperature on Hg2+ water decontamination using ETS-4 titanosilicate

    International Nuclear Information System (INIS)

    Batch stirred tank experiments were carried out to study the effect of pH (range 2-10, at 294 K) and temperature (277, 294 and 313 K, at pH 5) on the uptake of Hg2+ ions by ETS-4 microporous titanosilicate. Changes in the pH have a significant effect on the ETS-4 uptake efficiency, the optimal range being 4-6. Due to competition effects, the chemical used to adjust the pH of the Hg2+ solution also influences the uptake efficiency. Thermodynamic parameters for the uptake of Hg2+ ions were calculated. For the temperature range studied, the Hg2+ sorption increased with decreasing temperature.

  16. 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.

  17. Single Photon Sensitive HgCdTe Avalanche Photodiode Detector (APD) Project

    Data.gov (United States)

    National Aeronautics and Space Administration — A linear mode HgCdT electron-initiated avalanche photodiode (EAPD) capable of 1570nm photon detection efficiency (PDE) at >10 MHz will be developed. The Phase I...

  18. Thermal Diffusivity and Conductivity of Hg(1-x)Zn(x)Te Solids and Melts

    Science.gov (United States)

    Sha, Yi-Gao; Su, Ching-Hua; Mazuruk, K.; Lehoczky, S. L.

    1996-01-01

    The thermal diffusivity of pseudobinary Hg(1-x)Zn(x)Te solids and melts was measured by the laser flash method. The measured diffusivities for the solids of 0.10 less than or equal to x less than or equal to 0.30 are about 60% of that of the HgTe solid. Those for the melts rise rapidly with temperature but less so with increasing x. For x = 0.30, the diffusivity of the melt is about one third of that of the HgTe melt. Using the calculated beat capacity data from the associated solution model and measured density values, the thermal conductivity for the pseudobinary Hg(1-x)Zn(x)Te solids of 0.10 less than or equal to x less than or equal to 0.30 and for the melts of x = O.10, 0.16, and 0.30 was determined.

  19. Toxic and essential elements changed in black-legged kittiwakes (Rissa tridactyla) during their stay in an Arctic breeding area

    Energy Technology Data Exchange (ETDEWEB)

    Øverjordet, Ida Beathe, E-mail: ida.beathe.overjordet@sintef.no [Norwegian University of Science and Technology (NTNU), Department of Biology, N-7491 Trondheim (Norway); Kongsrud, Magnus Brunvoll [Norwegian University of Science and Technology (NTNU), Department of Biology, N-7491 Trondheim (Norway); Gabrielsen, Geir Wing [Norwegian Polar Institute, N-9296 Tromsø (Norway); Berg, Torunn [NTNU, Department of Chemistry, N-7491 Trondheim (Norway); Ruus, Anders [Norwegian Institute for Water Research (NIVA), N-0349 Oslo (Norway); Evenset, Anita [Akvaplan-niva, Fram Centre, N-9296 Tromsø (Norway); Faculty of Biosciences, Fisheries and Economics, UiT The Arctic University of Norway (Norway); Borgå, Katrine [Norwegian Institute for Water Research (NIVA), N-0349 Oslo (Norway); Department of Biosciences, University of Oslo (Norway); Christensen, Guttorm [Akvaplan-niva, Fram Centre, N-9296 Tromsø (Norway); Jenssen, Bjørn Munro [Norwegian University of Science and Technology (NTNU), Department of Biology, N-7491 Trondheim (Norway)

    2015-01-01

    Seasonal fluctuations in mercury (Hg), cadmium (Cd), zinc (Zn), copper (Cu) and selenium (Se) concentrations were studied in black-legged kittiwakes (Rissa tridactyla) from Kongsfjorden, Svalbard (79°57′N, 12°12′E). Element concentrations were determined in muscle and liver tissue in kittiwakes collected in May, July and October 2007. Stable isotopes of carbon (δ{sup 13}C) and nitrogen (δ{sup 15}N) were analysed in muscle tissue to calculate trophic position (TP) and examine the possible influence of carbon source on element accumulation. Metallothionein (MT) concentrations in liver, as well as Hg and Cd concentration in size-fractionated liver supernatant were determined to evaluate the association between elements and MT. Mercury concentrations declined from May through July to October in both tissues, while concentrations of Cd were similar in May and July and lower in October. A decline in TP between May and July, indicating a shift from fish-based diet towards an invertebrate-based diet explains the declining Hg concentration. The low Hg and Cd concentrations in October may be a result of an increased elimination, probably related to moulting. Selenium decreased in the same manner as Hg in liver and muscle, possibly related to the formation of Se–Hg complexes. Zinc and Cu did not fluctuate in muscle tissue, whereas hepatic Zn concentrations where highest in May. Hepatic Zn concentrations were higher in females compared to males in May, possibly related to egg production. Hepatic MT concentrations were lower in October compared to July, following the same trend as Hg and Cd. Cadmium was predominantly bound to the MT fraction of proteins in liver tissue, whereas Hg was associated with the larger proteins, indicating that MT was not sequestering Hg in the kittiwakes. - Highlights: • Seasonality of Cd and Hg is closely related to seasonal dietary changes. • Migration patterns influence the accumulation of Hg and Cd. • The seasonality of Se and Hg

  20. Growth, Characterization and Theoretical Study of a Novel Organometallic Nonlinear Optical Crystal: CdHg(SCN)4(C2H5NO)2

    Science.gov (United States)

    Liu, X. T.; Wang, X. Q.; Lin, X. J.; Sun, G. H.; Zhang, G. H.; Xu, D.

    2012-06-01

    A novel potentially useful second harmonic generation (SHG) organometallic nonlinear optical (NLO) crystal: cadmium mercury thiocyanate bis( N-methylformamide), CdHg(SCN)4(C2H5NO)2 (CMTN), has been prepared, and large high-optical-quality single crystals with dimensions up to 30 ×27×9 mm3 have been grown by the temperature-lowering method. Its structural, physicochemical and optical properties are characterized by elemental analyses, X-ray powder diffraction, Fourier transform infrared and Raman spectroscopy, thermal analysis, powder SHG measurements and UV/Vis/NIR transmission. The specific heat has been determined to be 515.5 J mol-1 K-1 at 300 K. CMTN possesses good physicochemical stability up to 128.5∘C, exhibits powder SHG efficiencies 0.8 times that of urea and its UV transparency cutoff is 358 nm. By the use of the DFT/B3LYP/6-31G(d) method, the microscopic second order NLO behavior of CMTN has been investigated by computing the first-order hyperpolarizability together with that of CdHg(SCN)4 (CMTC) and CdHg(SCN)4(C3H8O2) (CMTG) crystals. The results have been explained based on their crystal structures.

  1. Application of Neutron Activation Analysis for Determination of As, Cr, Hg, and Se in Mosses in the Metropolitan Area of the Valley of Toluca, Mexico

    Directory of Open Access Journals (Sweden)

    R. Mejía-Cuero

    2015-01-01

    Full Text Available This research presents a study of environmental monitoring at different sampling sites from the Metropolitan Area of the Valley of Toluca (MAVT, Mexico, using mosses (Leskea angustata (Tayl. and Fabronia ciliaris (Brid. and soil samples. The epiphytic mosses and soils were sampled in two campaigns within two periods of the year, a rainy and dry-cold season. The selected sampling sites included urban regions (UR, transitional regions (TR, and protected natural areas (PA. The samples were analyzed by the Instrumental Neutron Activation Analysis (INAA to determine As, Cr, Hg, and Se principally. However, due to the versatility of the analytic technique used, other elements including Cs, Co, Sc, Sb, Rb, Ce, La, Eu, and Yb were also detected. Statistical analysis (As, Cr, Hg, and Se was carried out with principal components and cluster analysis methods; this revealed that a good correlation exists between metal content in mosses and the degree of pollution in the areas sampled. The obtained results in mosses showed that the concentrations of As, Cr, Co, Cs, Rb, Ce, La, and Yb increased with respect to the concentrations obtained during the first sampling, whereas Se, Sc, Sb and Eu, concentrations were decreased. For As and Hg, the concentrations were similar in both sampling periods. The soil samples present the most significant concentration.

  2. A hybrid mesoporous material functionalized by 1,8-naphthalimide-base receptor and the application as chemosensor and absorbent for Hg2+ in water.

    Science.gov (United States)

    Meng, Qingtao; Zhang, Xiaolin; He, Cheng; Zhou, Peng; Su, Weiping; Duan, Chunying

    2011-03-15

    A novel hybrid material (SBA-P1) is prepared through the functionalization of mesoporous silica (SBA-15) with a 1,8-naphthalimide-based dye by sol-gel reaction. The characterization results of elemental analysis (EA), X-ray powder diffractometer (XRD) and spectroscopic methods demonstrate the fluorescence dye P1 is successfully grafted onto the inner surface of SBA-15 and the organized structure is preserved. SBA-P1 can detect Hg(2+) with high selectivity to Cu(2+), Zn(2+), Cd(2+), Pb(2+), Mn(2+), Ni(2+), Co(2+), Ag(+), Cr(3+), and Mg(2+), Ca(2+), Li(+), Na(+), K(+) in water and sensitivity to environmentally relevant mercury in complex natural samples. The quenching fluorescence detection is also reversible by treating with EDTA/base. Furthermore, its fluorescence intensity keeps stable in the physiologically relevant pH range. The extraction ability of SBA-P1 is also estimated by inductively coupled plasma source mass spectrometer (ICP), showing that approximately 90% of the Hg(2+) ion is extracted. These results imply that the hybrid material has potential application for sensing and removing of Hg(2+) ions in waste water and working as toxicide for acute mercury poisoning. PMID:21315897

  3. Insight into the unique oxidation chemistry of elemental mercury by chlorine-containing species: experiment and simulation.

    Science.gov (United States)

    Byun, Youngchul; Cho, Moohyun; Namkung, Won; Lee, Kiman; Koh, Dong Jun; Shin, Dong Nam

    2010-03-01

    This work investigated the oxidation chemistry of elemental mercury (Hg(0)) by chlorine-containing species produced indirectly through the gas-to-solid phase reaction between NO(x) gases and NaClO(2) powder (NaClO(2)(s)), where both experiment and simulation results were compared to clarify which species are responsible for the oxidation of Hg(0). At first, we introduced 30 ppm of NO(2) into the pack-bed reactor containing NaClO(2)(s) to produce OClO species and then injected NO and Hg(0) (260 microg/Nm(3)) to Mixer, where the concentration of NO was varied up to 180 ppm and the reaction temperature was set to 130 degrees C. We observed for the first time that the degree of Hg(0) oxidation is completely controlled by the introduced concentration of NO: for example, the oxidation efficiency of Hg(0) is drastically increased to become 100% at near 7 ppm NO, but further increasing NO concentration results in the oxidation efficiency of Hg(0) being gradually decreased. The simulation results indicated that such a propensity of Hg(0) oxidation efficiency to NO concentration can be attributed to the NO concentration-dependent Cl, ClO, and Cl(2) formation which plays a critical role in the oxidation of Hg(0). PMID:20131790

  4. Qualitative analysis of As, Ba, Cd, Cr, Zn, Fe, Mn, K, Hg, Pb y Cu, as constituents of Amatitlan Lake sediment by XRF

    International Nuclear Information System (INIS)

    Samples of fifteen sampling points were analyzed. Molybdenum X-ray tube with secondary excitation assembly, SiLi detector and deconvolution software AXIL were employed; self-standardization method based upon incoherent ratio was used for quantitative analysis of some elements. Ca, P, S, Ti, Mn, Fe, Cr, Zn, Cu, Ni, Ga, As, Pb, Ge, Sr and Pb, were found. As, Pb and Cu concentrations lower than 109 mg/lt, 119 mg/lt, and 500mg/lt, respectively, were measured. Hg was not detected. (author)

  5. Thermodynamic properties of the liquid Hg-Tl alloys determined from vapour pressure measurements

    Directory of Open Access Journals (Sweden)

    Gierlotka W.

    2002-01-01

    Full Text Available The partial vapour pressure of mercury over liquid Hg-Tl liquid solutions were determined in the temperature range from 450 to 700 K by direct vapour pressure measurements carried out with the quartz gauge. From the measured ln pHg vs. T relationships activities of mercury were determined. Using Redlich-Kister formulas logarithms of the activity coefficients were described with the following equations: From which all thermodynamic functions in the solutions can be derived.

  6. Screening of native plant species for phytoremediation potential at a Hg-contaminated mining site.

    Science.gov (United States)

    Marrugo-Negrete, José; Marrugo-Madrid, Siday; Pinedo-Hernández, José; Durango-Hernández, José; Díez, Sergi

    2016-01-15

    Artisanal and small-scale gold mining (ASGM) is the largest sector of demand for mercury (Hg), and therefore, one of the major sources of Hg pollution in the environment. This study was conducted in the Alacrán gold-mining site, one of the most important ASGM sites in Colombia, to identify native plant species growing in Hg-contaminated soils used for agricultural purposes, and to assess their potential as phytoremediation systems. Twenty-four native plant species were identified and analysed for total Hg (THg) in different tissues (roots, stems, and leaves) and in underlying soils. Accumulation factors (AF) in the shoots, translocation (TF) from roots to shoots, and bioconcentration (BCF) from soil-to-roots were determined. Different tissues from all plant species were classified in the order of decreasing accumulation of Hg as follows: roots > leaves > stems. THg concentrations in soil ranged from 230 to 6320 ng g(-1). TF values varied from 0.33 to 1.73, with high values in the lower Hg-contaminated soils. No correlation was found between soils with low concentrations of Hg and plant leaves, indicating that TF is not a very accurate indicator, since most of the Hg input to leaves at ASGM sites comes from the atmosphere. On the other hand, the BCF ranged from 0.28 to 0.99, with Jatropha curcas showing the highest value. Despite their low biomass production, several herbs and sub-shrubs are suitable for phytoremediation application in the field, due to their fast growth and high AF values in large and easily harvestable plant parts. Among these species, herbs such as Piper marginathum and Stecherus bifidus, and the sub-shrubs J. curcas and Capsicum annuum are promising native plants with the potential to be used in the phytoremediation of soils in tropical areas that are impacted by mining. PMID:26556744

  7. Observations of atmospheric Hg species and depositions in remote areas of China

    OpenAIRE

    Feng X; Fu X.; Zhang H.

    2013-01-01

    From September 2007, we conducted continuous measurements of speciated atmospheric mercury (Hg) and atmospheric mercury depositions at five remote sites in China. Four of these sites were involved in the Global Mercury Observation System (GMOS) as ground-based stations. These stations were located in the northwest, southwest, northeast, and east part of China, respectively, which represent the regional atmospheric Hg budgets in different areas of China. The preliminary results showed that mea...

  8. Optimization of magnetic powdered activated carbon for aqueous Hg(II) removal and magnetic recovery

    Energy Technology Data Exchange (ETDEWEB)

    Faulconer, Emily K., E-mail: emily.faulconer@yahoo.com [Department of Environmental Engineering Sciences, University of Florida, 217 Black Hall, P.O. Box 116450, Gainesville, FL 32611-645 (United States); Hoogesteijn von Reitzenstein, Natalia V.; Mazyck, David W. [Department of Environmental Engineering Sciences, University of Florida, 217 Black Hall, P.O. Box 116450, Gainesville, FL 32611-645 (United States)

    2012-01-15

    Highlights: Black-Right-Pointing-Pointer Thermal oxidation of MPAC decreased the amorphous characteristic of iron oxides. Black-Right-Pointing-Pointer Thermal oxidation did not influence magnetic recovery or Hg removal performance. Black-Right-Pointing-Pointer At all thermal oxidation temperatures, the 3:1 MPAC achieved the highest Hg removal. - Abstract: Activated carbon is known to adsorb aqueous Hg(II). MPAC (magnetic powdered activated carbon) has the potential to remove aqueous Hg to less than 0.2 {mu}g/L while being magnetically recoverable. Magnetic recapture allows simple sorbent separation from the waste stream while an isolated waste potentially allows for mercury recycling. MPAC Hg-removal performance is verified by mercury mass balance, calculated by quantifying adsorbed, volatilized, and residual aqueous mercury. The batch reactor contained a sealed mercury-carbon contact chamber with mixing and constant N{sub 2} (g) headspace flow to an oxidizing trap. Mercury adsorption was performed using spiked ultrapure water (100 {mu}g/L Hg). Mercury concentrations were obtained using EPA method 245.1 and cold vapor atomic absorption spectroscopy. MPAC synthesis was optimized for Hg removal and sorbent recovery according to the variables: C:Fe, thermal oxidation temperature and time. The 3:1 C:Fe preserved most of the original sorbent surface area. As indicated by XRD patterns, thermal oxidation reduced the amorphous characteristic of the iron oxides but did not improve sorbent recovery and damaged porosity at higher oxidation temperatures. Therefore, the optimal synthesis variables, 3:1 C:Fe mass ratio without thermal oxidation, which can achieve 92.5% ({+-}8.3%) sorbent recovery and 96.3% ({+-}9%) Hg removal. The mass balance has been closed to within approximately {+-}15%.

  9. How to keep the HG weights non-negative: the truncated Perceptron reweighing rule

    Directory of Open Access Journals (Sweden)

    Giorgio Magri

    2015-12-01

    Full Text Available The literature on error-driven learning in Harmonic Grammar (HG has adopted the Perceptron reweighing rule. Yet, this rule is not suited to HG, as it fails at ensuring non-negative weights. A variant is thus considered which truncates the updates at zero, keeping the weights non-negative. Convergence guarantees and error bounds for the original Perceptron are shown to extend to its truncated variant. 

  10. Magnetic properties of fluorinated Pb-doped Hg-1223 high Tc superconductors

    Energy Technology Data Exchange (ETDEWEB)

    Hamdan, N.M.; Sastry, P.V.P.S.S.; Schwartz, J.

    2001-09-23

    Fluorination of Pb-doped HgBa{sub 2}Ca{sub 2}Cu{sub 3}O{sub y} (Hg-1223) system was investigated. Structural and magnetic measurements reveal that fluorine addition promotes the phase formation, optimize the charge carrier concentration, and enhance flux pinning. We report an increase in both the transition temperature and the critical current density through controlled fluorine incorporation. Even a possible change in the pinning mechanism in this technologically important system is suggested.

  11. Screening of native plant species for phytoremediation potential at a Hg-contaminated mining site.

    Science.gov (United States)

    Marrugo-Negrete, José; Marrugo-Madrid, Siday; Pinedo-Hernández, José; Durango-Hernández, José; Díez, Sergi

    2016-01-15

    Artisanal and small-scale gold mining (ASGM) is the largest sector of demand for mercury (Hg), and therefore, one of the major sources of Hg pollution in the environment. This study was conducted in the Alacrán gold-mining site, one of the most important ASGM sites in Colombia, to identify native plant species growing in Hg-contaminated soils used for agricultural purposes, and to assess their potential as phytoremediation systems. Twenty-four native plant species were identified and analysed for total Hg (THg) in different tissues (roots, stems, and leaves) and in underlying soils. Accumulation factors (AF) in the shoots, translocation (TF) from roots to shoots, and bioconcentration (BCF) from soil-to-roots were determined. Different tissues from all plant species were classified in the order of decreasing accumulation of Hg as follows: roots > leaves > stems. THg concentrations in soil ranged from 230 to 6320 ng g(-1). TF values varied from 0.33 to 1.73, with high values in the lower Hg-contaminated soils. No correlation was found between soils with low concentrations of Hg and plant leaves, indicating that TF is not a very accurate indicator, since most of the Hg input to leaves at ASGM sites comes from the atmosphere. On the other hand, the BCF ranged from 0.28 to 0.99, with Jatropha curcas showing the highest value. Despite their low biomass production, several herbs and sub-shrubs are suitable for phytoremediation application in the field, due to their fast growth and high AF values in large and easily harvestable plant parts. Among these species, herbs such as Piper marginathum and Stecherus bifidus, and the sub-shrubs J. curcas and Capsicum annuum are promising native plants with the potential to be used in the phytoremediation of soils in tropical areas that are impacted by mining.

  12. CdTe and HgI2 crystals and detectors: present state and future

    International Nuclear Information System (INIS)

    After recalling the main properties of CdTe and HgI2 crystals from which the characteristics of these detectors will arise, the fabrication cycle is analysed at its various stages. The results at present achieved on CdTe and HgI2 detectors are analysed with a number of concrete applications in view such as medium power (0-200 keV) X and γ spectrometry, localisation of γ photons and solid ionisation chambers

  13. Reduced Limit on the Permanent Electric Dipole Moment of $^{199}$Hg

    OpenAIRE

    Graner, B.; Chen, Y.; Lindahl, E. G.; Heckel, B. R.

    2016-01-01

    This paper describes the results of the most recent measurement of the permanent electric dipole moment (EDM) of neutral $^{199}$Hg atoms. Fused silica vapor cells containing enriched $^{199}$Hg are arranged in a stack in a common magnetic field. Optical pumping is used to spin-polarize the atoms orthogonal to the applied magnetic field, and the Faraday rotation of near-resonant light is observed to determine an electric-field-induced perturbation to the Larmor precession frequency. Our resul...

  14. Gas-particle partitioning of atmospheric Hg(II and its effect on global mercury deposition

    Directory of Open Access Journals (Sweden)

    H. M. Amos

    2011-10-01

    Full Text Available Atmospheric deposition represents a major input of mercury to surface environments. The phase of mercury (gas or particle has important implications for its removal from the atmosphere. We use long-term observations of reactive gaseous mercury (RGM, particle-bound mercury (PBM, fine particulate matter (PM2.5, and temperature at five sites in North America to derive an empirical gas-particle partitioning relationship log10(K-1 = (10 ± 1 − (2500 ± 300/T where K = (PBM/PM2.5/RGM with PBM and RGM in common mixing ratio units, PM2.5 in μg m−3, and T in Kelvin. This relationship is in the range of previous work but is based on far more extensive data from multiple sites. We implement this empirical relationship in the GEOS-Chem global 3-D Hg model to partition divalent mercury (Hg(II. The resulting gas-phase fraction of Hg(II ranges from over 90% in warm air with little aerosol to less than 10% in cold air with high aerosol. Hg deposition to high latitudes increases because of more efficient scavenging of particulate Hg(II by snow. Model comparison to Hg observations at surface sites suggests that subsidence from the free troposphere (warm air, low aerosol is a major factor driving the seasonality of RGM, while elevated PBM is mostly associated with high aerosol loads. This and other model updates, including the correction of an outstanding algorithm error, to wet deposition improve the simulation of Hg wet deposition fluxes in the US relative to the previous version of the model. The observed wintertime minimum in wet deposition fluxes is attributed to inefficient snow scavenging of gas-phase Hg(II.

  15. Differential bioaccumulation of potentially toxic elements in benthic and pelagic food chains in Lake Baikal.

    Science.gov (United States)

    Ciesielski, Tomasz M; Pastukhov, Mikhail V; Leeves, Sara A; Farkas, Julia; Lierhagen, Syverin; Poletaeva, Vera I; Jenssen, Bjørn M

    2016-08-01

    Lake Baikal is located in eastern Siberia in the center of a vast mountain region. Even though the lake is regarded as a unique and pristine ecosystem, there are existing sources of anthropogenic pollution to the lake. In this study, the concentrations of the potentially toxic trace elements As, Cd, Pb, Hg, and Se were analyzed in water, plankton, invertebrates, and fish from riverine and pelagic influenced sites in Lake Baikal. Concentrations of Cd, Hg, Pb and Se in Lake Baikal water and biota were low, while concentrations of As were similar or slightly higher compared to in other freshwater ecosystems. The bioaccumulation potential of the trace elements in both the pelagic and the benthic ecosystems differed between the Selenga Shallows (riverine influence) and the Listvenichnyĭ Bay (pelagic influence). Despite the one order of magnitude higher water concentrations of Pb in the Selenga Shallows, Pb concentrations were significantly higher in both pelagic and benthic fish from the Listvenichnyĭ Bay. A similar trend was observed for Cd, Hg, and Se. The identified enhanced bioavailability of contaminants in the pelagic influenced Listvenichnyĭ Bay may be attributed to a lower abundance of natural ligands for contaminant complexation. Hg was found to biomagnify in both benthic and pelagic Baikal food chains, while As, Cd, and Pb were biodiluted. At both locations, Hg concentrations were around seven times higher in benthic than in pelagic fish, while pelagic fish had two times higher As concentrations compared to benthic fish. The calculated Se/Hg molar ratios revealed that, even though Lake Baikal is located in a Se-deficient region, Se is still present in excess over Hg and therefore the probability of Hg induced toxicity in the endemic fish species of Lake Baikal is assumed to be low. PMID:27130338

  16. Mercury (Hg) in meteorites: Variations in abundance, thermal release profile, mass-dependent and mass-independent isotopic fractionation

    Science.gov (United States)

    Meier, Matthias M. M.; Cloquet, Christophe; Marty, Bernard

    2016-06-01

    We have measured the concentration, isotopic composition and thermal release profiles of Mercury (Hg) in a suite of meteorites, including both chondrites and achondrites. We find large variations in Hg concentration between different meteorites (ca. 10 ppb to 14,000 ppb), with the highest concentration orders of magnitude above the expected bulk solar system silicates value. From the presence of several different Hg carrier phases in thermal release profiles (150-650 °C), we argue that these variations are unlikely to be mainly due to terrestrial contamination. The Hg abundance of meteorites shows no correlation with petrographic type, or mass-dependent fractionation of Hg isotopes. Most carbonaceous chondrites show mass-independent enrichments in the odd-numbered isotopes 199Hg and 201Hg. We show that the enrichments are not nucleosynthetic, as we do not find corresponding nucleosynthetic deficits of 196Hg. Instead, they can partially be explained by Hg evaporation and redeposition during heating of asteroids from primordial radionuclides and late-stage impact heating. Non-carbonaceous chondrites, most achondrites and the Earth do not show these enrichments in vapor-phase Hg. All meteorites studied here have however isotopically light Hg (δ202Hg = ∼-7 to -1) relative to the Earth's average crustal values, which could suggest that the Earth has lost a significant fraction of its primordial Hg. However, the late accretion of carbonaceous chondritic material on the order of ∼2%, which has been suggested to account for the water, carbon, nitrogen and noble gas inventories of the Earth, can also contribute most or all of the Earth's current Hg budget. In this case, the isotopically heavy Hg of the Earth's crust would have to be the result of isotopic fractionation between surface and deep-Earth reservoirs.

  17. A compare between myocardial topical negative pressure levels of -25 mmHg and -50 mmHg in a porcine model

    DEFF Research Database (Denmark)

    Lindstedt, Sandra; Paulsson, Per; Mokhtari, Arash;

    2008-01-01

    Topical negative pressure (TNP), widely used in wound therapy, is known to stimulate wound edge blood flow, granulation tissue formation, angiogenesis, and revascularization. We have previously shown that application of a TNP of -50 mmHg to the myocardium significantly increases microvascular blood...

  18. HgI2 nanostructures obtained hydrothermally for application in ionizing radiation detection

    Science.gov (United States)

    Pérez Barthaburu, María; Galain, Isabel; Aguiar, Ivana; Bentos Pereira, Heinkel; Fornaro, Laura

    2016-11-01

    The compound semiconductor HgI2 has been widely studied and employed as a material for ionizing radiation detection. Monocrystal growth is an intricate method for obtaining materials for this application. With the aim of finding a simpler and more effective way to develop ionizing radiation detectors, we employed HgI2 nanostructures subjected to a hydrothermal treatment and then pressed for this purpose. In the synthesis procedure, aqueous solutions of Hg(NO3)2 and NaI were mixed until their reaction completed and the suspension obtained was then placed in a homemade autoclave and heated at 120 °C for 2, 10 or 24 h. We confirmed the HgI2 tetragonal phase by powder XRD in all cases, independently of the synthesis conditions employed. Nanoparticles were characterized by their size and morphology by TEM. We used the HgI2 nanostructures to obtain a pellet by applying 0.7 GPa of pressure at room temperature. The pellet was then used to construct the detector, and we studied the electrical properties of the detector and its response to 241Am sources of different exposure rates. The resistivity and signal-to-noise ratio obtained are of the order of those reported for HgI2 detectors assembled with monocrystals. The results obtained in this work encourage us to work further on this topic, improving the method, scaling the detector’s size and studying its spectrometric grade.

  19. Production, separation and speciation of no-carrier-added Hg radionuclides using greener methodologies

    Energy Technology Data Exchange (ETDEWEB)

    Mandal, S.; Nayak, D. [Chemical Sciences Div., Saba Inst. of Nuclear Physics, Kolkata (India)

    2010-07-01

    Species dependent studies of no-carrier-added (nca) mercury were carried out using radioanalytical technique coupled with two greener analytical methodologies. The adsorption of nca {sup 195mg}Hg and {sup 197m}Hg radionuclides on chitosan biopolymer and cloud point extraction (CPE) was studied to develop environmentally sustainable speciation methodologies at ultra trace level. Species information was obtained by comparing the adsorption profile of nca radiomercury on chitosan biopolymer with the software code CHEAQS PRO. Results obtained from the adsorption study were validated by CPE technique using non ionic surfactant and mixed micelle. Both the experiments established that nca Hg existed as Hg(II). The experimental results support the presence of HgCl{sub 2} species over the pH range 2-4, whereas Hg(OH){sub 2} is the main species over the pH range 6-8. Chitosan biopolymer and mixed micelle [Triton-X-114 and cetyltrimethylammonium bromide (CTAB)] constitute an efficient reagent for the preconcentration of ultra trace level mercury. (orig.)

  20. Optimization of magnetic powdered activated carbon for aqueous Hg(II) removal and magnetic recovery.

    Science.gov (United States)

    Faulconer, Emily K; von Reitzenstein, Natalia V Hoogesteijn; Mazyck, David W

    2012-01-15

    Activated carbon is known to adsorb aqueous Hg(II). MPAC (magnetic powdered activated carbon) has the potential to remove aqueous Hg to less than 0.2 μg/L while being magnetically recoverable. Magnetic recapture allows simple sorbent separation from the waste stream while an isolated waste potentially allows for mercury recycling. MPAC Hg-removal performance is verified by mercury mass balance, calculated by quantifying adsorbed, volatilized, and residual aqueous mercury. The batch reactor contained a sealed mercury-carbon contact chamber with mixing and constant N(2) (g) headspace flow to an oxidizing trap. Mercury adsorption was performed using spiked ultrapure water (100 μg/L Hg). Mercury concentrations were obtained using EPA method 245.1 and cold vapor atomic absorption spectroscopy. MPAC synthesis was optimized for Hg removal and sorbent recovery according to the variables: C:Fe, thermal oxidation temperature and time. The 3:1 C:Fe preserved most of the original sorbent surface area. As indicated by XRD patterns, thermal oxidation reduced the amorphous characteristic of the iron oxides but did not improve sorbent recovery and damaged porosity at higher oxidation temperatures. Therefore, the optimal synthesis variables, 3:1 C:Fe mass ratio without thermal oxidation, which can achieve 92.5% (± 8.3%) sorbent recovery and 96.3% (± 9%) Hg removal. The mass balance has been closed to within approximately ± 15%. PMID:22104766

  1. Progress, challenges, and opportunities for HgCdTe infrared materials and detectors

    Science.gov (United States)

    Lei, Wen; Antoszewski, Jarek; Faraone, Lorenzo

    2015-12-01

    This article presents a review on the current status, challenges, and potential future development opportunities for HgCdTe infrared materials and detector technology. A brief history of HgCdTe infrared technology is firstly summarized and discussed, leading to the conclusion that HgCdTe-based infrared detectors will continue to be a core infrared technology with expanded capabilities in the future due to a unique combination of its favourable properties. Recent progress and the current status of HgCdTe infrared technology are reviewed, including material growth, device architecture, device processing, surface passivation, and focal plane array applications. The further development of infrared applications requires that future infrared detectors have the features of lower cost, smaller pixel size, larger array format size, higher operating temperature, and multi-band detection, which presents a number of serious challenges to current HgCdTe-based infrared technology. The primary challenges include well controlled p-type doping, lower cost, larger array format size, higher operating temperature, multi-band detection, and advanced plasma dry etching. Various new concepts and technologies are proposed and discussed that have the potential to overcome the existing primary challenges that are inhibiting the development of next generation HgCdTe infrared detector technology.

  2. Reduced Limit on the Permanent Electric Dipole Moment of $^{199}$Hg

    CERN Document Server

    Graner, B; Lindahl, E G; Heckel, B R

    2016-01-01

    This paper describes the results of the most recent measurement of the permanent electric dipole moment (EDM) of neutral $^{199}$Hg atoms. Fused silica vapor cells containing enriched $^{199}$Hg are arranged in a stack in a common magnetic field. Optical pumping is used to spin-polarize the atoms orthogonal to the applied magnetic field, and the Faraday rotation of near-resonant light is observed to determine an electric-field-induced perturbation to the Larmor precession frequency. Our results for this frequency shift are consistent with zero; we find the corresponding $^{199}$Hg EDM $d_{Hg} = (-2.20 \\pm 2.75_{stat} \\pm 1.48_{syst}) \\times 10^{-30} e\\cdot \\text{cm}$. We use this result to place a new upper limit on the $^{199}$Hg EDM $|d_{Hg}| < 7.4\\times 10^{-30} e\\cdot \\text{cm}$ (95\\% C.L.), improving our previous limit by a factor of 4. We also discuss the implications of this result for various $CP$-violating observables as they relate to theories of physics beyond the standard model.

  3. The influence of oxygen content on the Tc of HTS Hg-1245

    International Nuclear Information System (INIS)

    We have observed an extraordinary behavior oh the Hg Ba2Ca4 Cu5 O12+δ layered HTS (phase 1245) in the over doped state. Earlier we have synthesized the phase Hg-1245 with different oxygen content and consequently different values of the lattice parameter a. We have observed a coincidence of a values when the Tc(a) cupolas reach their maxima for phases Hg-1223, 1234, 1245 and a merging of their over doped parts together with abrupt falling off of the Tc values. The Hg-1245 phase has shown the most unusual behavior. Contrary to other phases, this one contains three types of Cu O2 layers in a unit cell. We supposed that, in the case of the Hg-1245 phase, the holes coming from the reservoir, which is the Hg-O plane, cannot reach the 'far' Cu O2 layer which is notable for this phase. We have calculated the hole concentration for each layer for 1223, 1234 and 1245 phases. The hole concentration appears negligibly small for the over doped 1245 phase. We can consider the 'fifth' Cu O2 layer as not taking part in superconductivity. The analysis of the behavior of the Tc(a) cupolas for the phases with different number of Cu O2 layers and of hole density distribution between the layers has been carried out

  4. Recent progress in MBE grown HgCdTe materials and devices at UWA

    Science.gov (United States)

    Gu, R.; Lei, W.; Antoszewski, J.; Madni, I.; Umana-Menbreno, G.; Faraone, L.

    2016-05-01

    HgCdTe has dominated the high performance end of the IR detector market for decades. At present, the fabrication costs of HgCdTe based advanced infrared devices is relatively high, due to the low yield associated with lattice matched CdZnTe substrates and a complicated cooling system. One approach to ease this problem is to use a cost effective alternative substrate, such as Si or GaAs. Recently, GaSb has emerged as a new alternative with better lattice matching. In addition, implementation of MBE-grown unipolar n-type/barrier/n-type detector structures in the HgCdTe material system has been recently proposed and studied intensively to enhance the detector operating temperature. The unipolar nBn photodetector structure can be used to substantially reduce dark current and noise without impeding photocurrent flow. In this paper, recent progress in MBE growth of HgCdTe infrared material at the University of Western Australia (UWA) is reported, including MBE growth of HgCdTe on GaSb alternative substrates and growth of HgCdTe nBn structures.

  5. Comparison experiments of neon and helium buffer gases cooling in trapped 199Hg+ ions linear trap

    International Nuclear Information System (INIS)

    The influences of different buffer gas, neon and helium, on 199Hg+ clock transition are compared in trapped 199Hg+linear trap. By the technique of time domain's Ramsey separated oscillatory fields, the buffer gas pressure frequency shifts of 199Hg+ clock transition are measured to be (df/dPNe)(1/f) = 1.8 × 10−8 Torr−1 for neon and (df/dPHe)(1/f) = 9.1×10−8 Torr−1 for helium. Meanwhile, the line-width of 199Hg+ clock transition spectrum with the buffer gas neon is narrower than that with helium at the same pressure. These experimental results show that neon is a more suitable buffer gas than helium in 199Hg+ ions microwave frequency standards because of the 199Hg+ clock transition is less sensitive to neon variations and the better cooling effect of neon. The optimum operating pressure for neon is found to be about 1.0×10−5 Torr in our linear ion trap system. (atomic and molecular physics)

  6. Hg concentrations and related risk assessment in coral reef crustaceans, molluscs and fish from New Caledonia

    Energy Technology Data Exchange (ETDEWEB)

    Chouvelon, Tiphaine [Littoral Environnement et Societes (LIENSs), UMR 6250, CNRS-Universite La Rochelle, 2 Rue Olympe de Gouges, F-17042 La Rochelle Cedex 01 (France); Warnau, Michel [International Atomic Energy Agency-Marine Environment Laboratories (IAEA-MEL), 4 Quai Antoine Ier, MC-98000 (Monaco); Churlaud, Carine [Federation de Recherche en Environnement pour le Developpement Durable (FR-EDD), FR CNRS 3097, Centre Commun d' Analyses, 5 Perspectives de l' Ocean, F-17071 La Rochelle Cedex 9 (France); Bustamante, Paco [Littoral Environnement et Societes (LIENSs), UMR 6250, CNRS-Universite La Rochelle, 2 Rue Olympe de Gouges, F-17042 La Rochelle Cedex 01 (France)], E-mail: pbustama@univ-lr.fr

    2009-01-15

    There is a dramatic lack of data on Hg levels in marine organisms from tropical areas, and in particular from New Caledonia. For the first time, this study reports the total Hg concentrations in the tissues of several marine taxa from the New Caledonian lagoon. Seafood from both wild and farmed populations was considered. Hg concentrations varied over three orders of magnitudes according to factors including species, age (size/weight), trophic level, lifestyle and geographical origin. Taking into account the edible tissues, estimations of the amount of flesh that should be consumed by a 60-kg person to reach the Hg Provisional Tolerable Weekly Intake (PTWI) reveal acceptable risk for Human health in general. However, a risk was clearly identified in one site of the lagoon (i.e. Grande Rade) where high Hg concentrations were measured. These concentrations were higher than values reported in the current literature. - This work reports the first assessment of Hg levels in edible organisms from the New Caledonian lagoon and the associated risk linked to their consumption by Human.

  7. Factors affecting Hg (II adsorption in soils from the Rio Negro basin (Amazon

    Directory of Open Access Journals (Sweden)

    Patricia Miretzky

    2005-06-01

    Full Text Available Mercury (II adsorption studies in top soils (top 10 cm from the Rio Negro basin show this process depends strongly on some selected parameters of the aqueous phase in contact with the soils. Maximum adsorption occurred in the pH range 3.0-5.0 (>90%. Dissolved organic matter shows an inhibitory effect on the availability of Hg (II to be adsorbed by the soils, whereas a higher chloride content of the solution resulted in a lower adsorption of Hg (II at pH 5.0. Soils with higher organic matter content were less affected by changes in the salinity. An increase in the initial Hg (II concentration increased the amount of Hg (II adsorbed by the soil and decreased the time needed to reach equilibrium. A Freundlich isotherm provided a good model for Hg (II adsorption in the two types of soil studied. The kinetics of Hg (II adsorption on Amazonian soils showed to be very fast and followed pseudo-second order kinetics. An environmental implication of these results is discussed under the real scenario present in the Negro River basin, where acidic waters are in contact with a soil naturally rich in mercury.

  8. Reduced Limit on the Permanent Electric Dipole Moment of ^{199}Hg.

    Science.gov (United States)

    Graner, B; Chen, Y; Lindahl, E G; Heckel, B R

    2016-04-22

    This Letter describes the results of the most recent measurement of the permanent electric dipole moment (EDM) of neutral ^{199}Hg atoms. Fused silica vapor cells containing enriched ^{199}Hg are arranged in a stack in a common magnetic field. Optical pumping is used to spin polarize the atoms orthogonal to the applied magnetic field, and the Faraday rotation of near-resonant light is observed to determine an electric-field-induced perturbation to the Larmor precession frequency. Our results for this frequency shift are consistent with zero; we find the corresponding ^{199}Hg EDM d_{Hg}=(-2.20±2.75_{stat}±1.48_{syst})×10^{-30}e cm. We use this result to place a new upper limit on the ^{199}Hg EDM |d_{Hg}|<7.4×10^{-30}e cm (95% C.L.), improving our previous limit by a factor of 4. We also discuss the implications of this result for various CP-violating observables as they relate to theories of physics beyond the standard model. PMID:27152789

  9. Reduced Limit on the Permanent Electric Dipole Moment of Hg 199

    Science.gov (United States)

    Graner, B.; Chen, Y.; Lindahl, E. G.; Heckel, B. R.

    2016-04-01

    This Letter describes the results of the most recent measurement of the permanent electric dipole moment (EDM) of neutral Hg 199 atoms. Fused silica vapor cells containing enriched Hg 199 are arranged in a stack in a common magnetic field. Optical pumping is used to spin polarize the atoms orthogonal to the applied magnetic field, and the Faraday rotation of near-resonant light is observed to determine an electric-field-induced perturbation to the Larmor precession frequency. Our results for this frequency shift are consistent with zero; we find the corresponding Hg 199 EDM dHg=(-2.20 ±2.7 5stat±1.4 8syst)×10-30e cm . We use this result to place a new upper limit on the Hg 199 EDM |dHg|<7.4 ×10-30e cm (95% C.L.), improving our previous limit by a factor of 4. We also discuss the implications of this result for various C P -violating observables as they relate to theories of physics beyond the standard model.

  10. Trace elemental analysis of adenoma and carcinoma thyroid by PIXE method

    Science.gov (United States)

    Reddy, S. Bhuloka; John Charles, M.; Ravi Kumar, M.; Reddy, B. Seetharami; Anjaneyulu, Ch.; Naga Raju, G. J.; Sundareswar, B.; Vijayan, V.

    2002-11-01

    Trace elemental analysis was carried out in the biological samples of normal, adenoma and carcinoma thyroids using particle induced X-ray emission technique (PIXE). A 2 MeV proton beam was employed to excite the samples. The elements Cl, K, Ca, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, As, Sr, I, Hg and Pb were identified and their concentrations were estimated. The concentrations of the elements Ca, Cu, Zn, As, I and Hg are found to be much lower in carcinoma thyroid than those in the normal thyroid while the concentration of the elements K, Ti, V, Cr, Mn, Fe, Co and Sr in carcinoma thyroid are higher than the concentrations in normal thyroid. The lower and higher values of some of the elements in carcinoma thyroid may be attributed to some pathological factors.

  11. Glucometer-based quantitative determination of Hg(II) using gold particle encapsulated invertase and strong thymine-Hg(II)-thymine interaction for signal amplification

    International Nuclear Information System (INIS)

    We report on a simple and sensitive protocol for quantitative assay of Hg(II) ions. The process involves the following steps: A thymine (T)-rich single-stranded DNA1 is used to modify the surface of a well of a microplate by the use of biotin-avidin interface chemistry. In parallel, clusters of gold microspheres with a core containing the enzyme invertase were prepared and modified, via thiol chemistry, with a second T-rich oligomer (DNA2). If the gold clusters incorporating invertase and carrying DNA2 are added to the DNA1 immobilized in the wells of the microplate, no interaction will occur and the gold cluster will be removed in the subsequent washing step. If, however, Hg(II) is present in the sample, the DNA on the gold clusters incorporating the enzyme invertase will bind to the DNA in the wells due to the formation of strong T-Hg(II)-T links between the two DNA strands. The encapsulated invertase will not be removed in the following washing step. Sucrose is added in the next step along with invertase which will hydrolyze it to form glucose and fructose. The quantity of glucose formed increases with the quantity of Hg(II) ions present in the sample. The glucose generated is then quantified by using a commercial personal glucometer. Under optimal conditions, the signal for glucose increases with Hg(II) concentration in the range from 0.05 to 80 nM, and the detection limit is as low as 10 pM. The assay has good repeatability and shows an intermediate precision of down to 7.5 %. The method is highly specific for Hg(II) over other metal ions. It was applied to the determination of Hg(II) in naturally contaminated sewage and in spiked samples of drinking water. This approach has a wide scope of application in that it may be extended to numerous other kinds of nanoparticles, oligomer interactions, enzymes and ions. (author)

  12. Measuring Hg and MeHg fluxes from dynamic systems using high resolution in situ monitoring - case study: the Sacramento-San Joaquin Delta

    Science.gov (United States)

    Fleck, J. A.; Bergamaschi, B. A.; Downing, B. D.; Lionberger, M. A.; Schoellhamer, D.; Boss, E.; Heim, W.; Stephenson, M.

    2006-12-01

    Quantifying net loads in tidal systems is difficult, time consuming, and often very expensive. Owing to the relatively rapid nature of tidal exchange, numerous measurements are required in a brief amount of time to accurately quantify constituent fluxes between a tidal wetland and its surrounding waters. Further complicating matters, the differences in chemical concentrations of a constituent between the flood and ebb tides are often small, so that the net export of the constituent is orders of magnitude smaller than the bulk exchange in either direction over the tidal cycle. Thus, high-resolution sampling coupled with high-sensitivity instruments over an adequate amount of time is required to accurately determine a net flux. These complications are exacerbated for mercury species because of the difficulties related to clean sampling and trace-level analysis. The USGS currently is collecting data to determine the fluxes of total mercury (Hg) and methyl-Hg (MeHg) in dissolved and particulate phases at Browns Island in the San Francisco Bay-Delta, a tidally influenced estuarine system. Our field deployment package consists of an upward-looking current profiler to quantify water flux, and an array of other instruments measuring the following parameters: UV absorption, DO, pH, salinity, temperature, water depth, optical backscatter, fluorescence, and spectral attenuation. Measurements are collected at 30-minute intervals for seasonal, month-long deployments in the main slough of Brown's Island. We infer Hg and MeHg concentrations by using multivariate analysis of spectral absorbance and fluorescence properties of the continuous measurements, and comparing them to those of discrete samples taken hourly over a 25-hour tidal cycle for each deployment. Preliminary results indicate that in situ measurements can be used to predict MeHg concentrations in a tidal wetland slough in both the filtered (r2=0.96) and unfiltered (r2=0.95) fractions. Despite seasonal differences in

  13. Chemical identification and properties of element 112

    CERN Document Server

    Yakushev, A B; Zvára, I

    2002-01-01

    The second experiment on the chemical identification of element 112 performed at the FLNR (Dubna) is reported. Similar to the first test in 2000, the 2 mg/cm sup 2 sup n sup a sup t U target was bombarded with the 262-MeV sup 4 sup 8 Ca ions aiming at the production of sup 2 sup 8 sup 3 112, which as reported earlier decays by SF with a half-life of 3 min. The bombardment products recoiling from the target were thermalized in flowing helium and transported by the gas to detectors 25 m apart. Of all the heavy elements, the reaction products, only Hg, Rn and At were efficiently transported and thus selectively isolated. This time the beam dose was much higher (2.8 centre dot 10 sup 1 sup 8) and two different devices for detecting fission fragments and alpha particles were employed. The device used earlier was an assembly of sixteen PIPS detectors coated with Au to detect 'Hg-like' nuclides being adsorbed on Au at ambient temperature. The new one was a flow-through ionization chamber, 5000 cm sup 3 in volume, wh...

  14. 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)

    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)

  15. Relativistic effects on atomic and molecular properties of the heaviest elements

    Science.gov (United States)

    Pershina, V.; Anton, J.; Bastug, T.

    2007-10-01

    Interaction of superheavy element 112 and its homolog Hg with inert and gold surfaces was studied on the basis of atomic and molecular fully-relativistic (4-component) DFT electronic structure calculations. Performance of additional non-relativistic calculations allowed one to demonstrate the role and magnitude of relativistic effects on adsorption energies and bond distances of the studied systems. For example, on quartz, element 112 will be stronger adsorbed than Hg by about 5 kJ/mol (or at 5 degrees higher temperatures) due to the stronger van der Waals interaction. This is caused by the relativistically contracted smallest atomic radius of element 112. Non-relativistically, the trend would be opposite. On surface of gold, element 112 will be about 20 kJ/mol weaker adsorbed than Hg (i.e., it will be deposited at about 100 degrees lower temperatures than Hg). Such a decrease in Δ Hads comes at the account of the weaker interaction of the relativistically stabilized 7s1/2(112) orbital with valence orbitals of gold. Still, the relatively large adsorption energy of element 112 is indicative that it is a transition metal forming intermetallic compounds with Au and other metals due to the involvement of the relativistically destabilized 6d orbitals. The influence of relativistic effects on the adsorption energy depends, however, on the adsorption position.

  16. Trace Elements, With Special Reference to Mercury, in Fish Collected Upstream and Downstream of Los Alamos National Laboratory

    Energy Technology Data Exchange (ETDEWEB)

    P. R. Fresquez; J. D. Huchton; M. A. Mullen

    1999-11-01

    Trace elements (Ag, As, Ba, Be, Cr, Cd, Cu, Hg, Ni, Pb, Sb, Se, and Tl) were determined in muscle (fillet) of average sized fish (mostly carp, catfish, and sucker) collected from the confluences of major canyons that cross Los Alamos National Laboratory (LANL) lands with the Rio Grande (RG). Also, trace elements were determined in fish from reservoirs upstream (Abiquiu [AR]) and downstream (Cochiti [CR]) of LANL from 1991 through 1999. In general, all of the (mean) trace elements, including Hg, were either at the limits of detection (LOD) or in low concentrations at all study sites. Of the trace elements (e.g., Ba, Cu, and Hg) that were found to be above the LOD in fish muscle collected from LANL canyons/RG, none were in significantly higher (p < 0.05) concentrations than in muscle of fish collected from background locations. Mercury concentrations (mean of means) in fish from AR (all other trace elements were at LOD) were significantly higher (p < 0.10) than Hg concentrations in fish from CR, and Hg concentrations in fish collected from both reservoirs exhibited significantly (AR = p <0.05 and CR = p < 0.10) decreasing trends over time.

  17. The construction and testing of the portable Hg(2+) ultrasonic calibrator for the control of mercury speciation systems.

    Science.gov (United States)

    Gorecki, Jerzy; Okonska, Anna

    2016-01-15

    During fuel combustion mercury, as Hg(0) and Hg(2+) forms, is emitted to the atmosphere. Effective reduction of mercury emission requires applying speciation systems for emission control and research. An important part of all mercury determination and speciation systems are the calibrators. Calibrators are responsible for the accuracy of mercury determination and, in consequence, the effective reduction of mercury emission. The aim of the work was to construct a portable HgCl2 calibrator. The purpose of the device was the control of mercury speciation systems for continuous measurements and study of HgCl2 sorption. As a result of previously conducted research, the portable Hg(2+) ultrasonic calibrator was designed, constructed and tested. The ultrasonic calibrator generates a stable stream of HgCl2 (RSD=2.8% for CHg=28µg/m(3)). The correlation between theoretical and reading concentration of HgCl2 was R(2)=0.9983. The average recovery of HgCl2 was 95%. The advantages of the ultrasonic Hg(2+) calibrator are: high accuracy and selectivity, low pressure of HgCl2 stream and very low cost of production. The calibrator was successfully tested, both in the laboratory and in the power plant, during a preliminary study on HgCl2 sorption on a fly ash filter. PMID:26592572

  18. A colorimetric silver nanoparticle-based assay for Hg(II) using lysine as a particle-linking reagent

    International Nuclear Information System (INIS)

    We describe a colorimetric method for the determination of Hg(II) that is based on the aggregation of silver nanoparticles (AgNPs) in the presence of Hg(II) and lysine. If Hg(II) ions are added to unmodified AgNPs, they will deposit on the surface where they will be reduced to Hg(0) by NaBH4 to form a shell around the AgNPs. Upon addition of lysine to the Hg(II)-capped AgNPs, the aggregation of the AgNPs will be induced because the two amino groups of lysine have a high affinity for Hg(II). Aggregation results in a color change from orange to yellowish. The effect was exploited to design a colorimetric assay for Hg(II) that has a 1 nM detection limit. (author)

  19. Ultrasensitive detection of Hg2+ using oligonucleotide-functionalized AlGaN/GaN high electron mobility transistor

    International Nuclear Information System (INIS)

    An oligonucleotide-functionalized ion sensitive AlGaN/GaN high electron mobility transistor (HEMT) was fabricated to detect trace amounts of Hg2+. The advantages of ion sensitive AlGaN/GaN HEMT and highly specific binding interaction between Hg2+ and thymines were combined. The current response of this Hg2+ ultrasensitive transistor was characterized. The current increased due to the accumulation of Hg2+ ions on the surface by the highly specific thymine-Hg2+-thymine recognition. The dynamic linear range for Hg2+ detection has been determined in the concentrations from 10−14 to 10−8 M and a detection limit below 10−14 M level was estimated, which is the best result of AlGaN/GaN HEMT biosensors for Hg2+ detection till now.

  20. Growth, structure and optical properties of Tl4HgBr6 single crystals

    Science.gov (United States)

    Khyzhun, O. Y.; Kityk, I. V.; Piasecki, M.; Fedorchuk, A. O.; Levkovets, S. I.; Fochuk, P. M.; Myronchuk, G. L.; Parasyuk, O. V.

    2015-12-01

    Tl4HgBr6 single crystals were grown using solution-fusion method. The crystal structure of the ternary bromide was refined. Tl4HgBr6 crystallizes in the non-centrosymmetric space group P4nc with the lattice parameters a=8.9539(8) Å and c=8.7884(8) Å and it is isostructural to the Tl4HgI6 compound. The non-centrosymmetric structure of the Tl4HgBr6 compound was also confirmed by the existence of a modest second harmonic generation effect (0.4-0.5 pm/V) and by the value of piezoelectric coefficient (0.9 pm/V). The electronic structure of Tl4HgBr6 was explored using X-ray photoelectron spectroscopy (XPS) and X-ray emission spectroscopy (XES). In particular, for the Tl4HgBr6 crystal, we have measured XPS core-level and valence-band spectra for both pristine and Ar+ ion-bombarded surfaces. The XPS data reveal low hygroscopicity of Tl4HgBr6, the property that is very important when handling this material in optoelectronic devices working at ambient conditions. The present XPS data indicate that the Tl4HgBr6 single crystal surface is rather sensitive with respect to Ar+ ion-bombardment: such a treatment reduces significantly mercury content in the topmost surface layers. Comparison on a common energy scale of the XPS valence-band spectrum of Tl4HgBr6 and the XE Br Kβ2 band, representing peculiarities of the energy distribution of the Br 4 p states, reveals that the main contribution of the valence Br p states occurs in the upper portion of the valence band, with also their significant contributions in other valence band regions. The measurements of spectral distribution of the absorption coefficient indicate that the Tl4HgBr6 compound is a semiconductor with the bandgap energy value of 2.43 eV at 300 K, and the bandgap energy increases up to 2.48 eV when temperature decreases to 100 K.