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Sample records for ag pb zn

  1. Bioleaching mechanism of Zn, Pb, In, Ag, Cd and As from Pb/Zn smelting slag by autotrophic bacteria.

    PubMed

    Wang, Jia; Huang, Qifei; Li, Ting; Xin, Baoping; Chen, Shi; Guo, Xingming; Liu, Changhao; Li, Yuping

    2015-08-15

    A few studies have focused on release of valuable/toxic metals from Pb/Zn smelting slag by heterotrophic bioleaching using expensive yeast extract as an energy source. The high leaching cost greatly limits the practical potential of the method. In this work, autotrophic bioleaching using cheap sulfur or/and pyrite as energy matter was firstly applied to tackle the smelting slag and the bioleaching mechanisms were explained. The results indicated autotrophic bioleaching can solubilize valuable/toxic metals from slag, yielding maximum extraction efficiencies of 90% for Zn, 86% for Cd and 71% for In, although the extraction efficiencies of Pb, As and Ag were poor. The bioleaching performance of Zn, Cd and Pb was independent of leaching system, and leaching mechanism was acid dissolution. A maximum efficiency of 25% for As was achieved by acid dissolution in sulfursulfur oxidizing bacteria (S-SOB), but the formation of FeAsO4 reduced extraction efficiency in mixed energy source - mixed culture (MS-MC). Combined works of acid dissolution and Fe(3+) oxidation in MS-MC was responsible for the highest extraction efficiency of 71% for In. Ag was present in the slag as refractory AgPb4(AsO4)3 and AgFe2S3, so extraction did not occur.

  2. Classification of Broken Hill-Type Pb-Zn-Ag Deposits: A Refinement

    NASA Astrophysics Data System (ADS)

    Spry, P. G.; Teale, G. S.; Steadman, J. A.

    2009-05-01

    Broken Hill Hill-type Pb-Zn-Ag (BHT) deposits constitute some of the largest ore deposits in the world. The Broken Hill deposit is the largest accumulation of Pb, Zn, and Ag on Earth and the Cannington deposit is currently the largest silver deposit. Characteristic features of BHT deposits include: 1. high Pb+Zn+Ag values with Pb > Zn; 2. Metamorphism to amphibolite-granulite facies; 3. Paleo-to Mesoprotoerozoic clastic metasedimentary host rocks; 4. Sulfides that are spatially associated with bimodal (felsic and mafic) volcanic rocks, and stratabound gahnite- and garnet-bearing rocks and iron formations, 5. Stacked orebodies with characteristic Pb:Zn:Ag ratios and skarn-like Fe-Mn-Ca-F gangue assemblages, and the presence of Cu, Au, Bi, As, and Sb; and 6. Sulfur-poor assemblages. Broken Hill (Australia) has a prominent footwall feeder zone whereas other BHT deposits have less obvious alteration zones (footwall garnet spotting and stratabound alteration haloes). Deposits previously regarded in the literature as BHT deposits are Broken Hill, Cannington, Oonagalabie, Menninie Dam, and Pegmont (Australia), Broken Hill, Swartberg, Big Syncline, and Gamsberg (South Africa), Zinkgruvan (Sweden), Sullivan, Cottonbelt, and Foster River (Canada), and Boquira (Brazil). Of these deposits, only the Broken Hill (Australia, South Africa), Pinnacles, Cannington, Pegmont, and Swartberg deposits are BHT deposits. Another BHT deposit includes the Green Parrot deposit, Jervois Ranges (Northern Territory). The Foster River, Gamsberg, and Sullivan deposits are considered to be "SEDEX deposits with BHT affinities", and the Oonagalabie, Green Mountain (Colorado), and Zinkgruvan are "VMS deposits with BHT affinities". In the Broken Hill area (Australia), Corruga-type Pb-Zn-Ag deposits occur in calc-silicate rocks and possess some BHT characteristics; the Big Syncline, Cottonbelt, Menninie Dam, and Saxberget deposits are Corruga-type deposits. SEDEX deposits with BHT affinities, VMS

  3. Geochemistry of the Patricia Zn-Pb-Ag Deposit (paguanta, NE Chile)

    NASA Astrophysics Data System (ADS)

    Chinchilla Benavides, D.; Merinero Palomares, R.; Piña García, R.; Ortega Menor, L.; Lunar Hernández, R.

    2013-12-01

    The Patricia Zn-Pb-Ag ore deposit is located within the Paguanta mining project, situated at the northern end of the Andean Oligocene Porphyry Copper Belt of Chile. The sulfide mineralization occurs as W-E oriented veins hosted in volcanic rocks, mainly andesite (pyroclastic, ash and lavas), of Upper Cretaceous to Middle Tertiary age. The ore mineralogy (obtained by EMPA analyses) comprises in order of abundance, pyrite, sphalerite (5.5 - 10.89 wt % Fe, 9.8-19 % molar FeS and 0.52 wt % Cd), galena, arsenopyrite, chalcopyrite and Ag-bearing sulfosalts. The veins show a zoned and banded internal structure with pyrite at the edges and sphalerite in the center. The Ag occurs mostly as Ag-Cu-Sb sulfosalts, in order of abundance: series freibergite - argentotennantite -polybasite and stephanite. Other minor Ag phases such as argentite, pyrargirite and diaphorite were also identified. These Ag phases are typically associated with the base-metal sulfides. Freibergite occurs filling voids within sphalerite, chalcopyrite and at the contact between sphalerite and galena. Polybasite, stephanite, pyrargirite and argentite are mostly in close association with freibergite. In the case of diaphorite, it commonly occurs filling voids between galena crystals or as inclusions within galena. Some minor Ag-bearing sulfosalts are also identified between pyrite crystals. The alteration minerals are dominated by chlorite, illite and kaolinite. The gangue minerals consist of quartz and carbonates identified by XRD as kutnahorite. We obtained linear correlation statistically significant only for Ag, As Au, Cd, Cu, Pb, Sb and Zn and therefore we generated an enhanced scatter plot matrix of these elements. Bulk rock analyses (ICP/MS and XRF) of drill cores show that Ag is strongly and positively correlated with Pb and As, moderately with Cd, Sb, Au and Zn and weakly with Cu, while Au is moderately and positively correlated with Ag, As, Cd, Sb and Zn and weakly with Cu and Pb. These results

  4. Possible Mesozoic age of Ellenville Zn-Pb-Cu(Ag) deposit, Shawangunk Mountains, New York

    USGS Publications Warehouse

    Friedman, J.D.; Conrad, J.E.; McKee, E.H.; Mutschler, F.E.; Zartman, R.E.

    1994-01-01

    Ore textures, epithermal open-space filling of Permian structures of the Alleghanian orogeny, and largely postorogenic mineralization of the Ellenville, New York, composite Zn-Pb-Cu(Ag) vein system, provide permissive evidence for post-Permian mineralization. Isochron ages determined by 40Ar/39Ar laser-fusion techniques for K-bearing liquid inclusions in main-stage quartz from the Ellenville deposit additionally suggest a Mesozoic time of mineralization, associated with extensional formation of the Newark basin. The best 40Ar/39Ar total-fusion age range is 165 ?? 30 to 193 ?? 35 Ma. The Mesozoic 40Ar/39Ar age agrees with that of many other dated northern Appalachian Zn-Pb-Cu(Ag) deposits with near-matching lead isotope ratios, and adds new evidence of Jurassic tectonism and mineralization as an overprint to Late Paleozoic tectonism at least as far north as Ellenville (lat. 41??43???N). ?? 1994 Springer-Verlag.

  5. Geology and mineralogy of the Santo Nino Ag-Pb-Zn vein, Fresnillo District, Mexico

    SciTech Connect

    Gemmell, J.B.; Zantop, H.; Birnie, R.W.

    1985-01-01

    The Santo Nino Ag-Pb-Zn vein is the major producer of the Fresnillo District, located 750 km NW of Mexico City. It is over 2.4 km long, more than 480 m in vertical extent, more than 2.5 m wide overall, and has average grades of >600 gm/t Ag and <2% combined Pb and Zn. The vein is hosted by a tilted sequence of Cretaceous graywackes, shales and andesitic volcanics and extends upward into a Lower Tertiary conglomerate. Up to 5 separate opening events occurred along the vein, resulting in discontinuous stages of brecciation and crustiform banding. Ore mineral zonation is well developed both vertically and laterally and closely reflects metal and metal ratio distributions. Ore minerals are sphalerite, galena, pyrite, chalcopyrite, arsenopyrite, marcasite, pyrrhotite, acanthite, native silver, and three coexisting solid solution series, pyrargyrite-proustite, polybasite-arsenopolybasite, and tetrahedrite-tennantite in a gangue of quartz, calcite, clay, sericite,and chlorite. A 5-stage paragenetic sequence can be established: 1) pyrite, arsenopyrite, quartz, 2) sphalerite, galena, chalcopyrite, quartz, 3) tetrahedrite, pyrargyrite, polybasite, quartz, 4) acanthite, native silver, calcite, quartz, and 5) calcite. Preliminary microprobe analyses indicate that the Ag-rich solid solution series are Sb-rich in the central and upper portions of the vein and As-rich at deeper levels.

  6. Pb isotopic constraints on the formation of the Dikulushi Cu-Pb-Zn-Ag mineralisation, Kundelungu Plateau (Democratic Republic of Congo)

    NASA Astrophysics Data System (ADS)

    Haest, Maarten; Schneider, Jens; Cloquet, Christophe; Latruwe, Kris; Vanhaecke, Frank; Muchez, Philippe

    2010-04-01

    Base metal-Ag mineralisation at Dikulushi and in other deposits on the Kundelungu Plateau (Democratic Republic of Congo) developed during two episodes. Subeconomic Cu-Pb-Zn-Fe polysulphide ores were generated during the Lufilian Orogeny (c. 520 Ma ago) in a set of E-W- and NE-SW-oriented faults. Their lead has a relatively unradiogenic and internally inhomogeneous isotopic composition (206Pb/204Pb = 18.07-18.49), most likely generated by mixing of Pb from isotopically heterogeneous clastic sources. These sulphides were remobilised and enriched after the Lufilian Orogeny, along reactivated and newly formed NE-SW-oriented faults into a chalcocite-dominated Cu-Ag mineralisation of high economic interest. The chalcocite samples contain only trace amounts of lead and show mostly radiogenic Pb isotope signatures that fall along a linear trend in the 207Pb/204Pb vs. 206Pb/204Pb diagram (206Pb/204Pb = 18.66-23.65; 207Pb/204Pb = 15.72-16.02). These anomalous characteristics reflect a two-stage evolution involving admixture of both radiogenic lead and uranium during a young fluid event possibly c. 100 Ma ago. The Pb isotope systematics of local host rocks to mineralisation also indicate some comparable young disturbance of their U-Th-Pb systems, related to the same event. They could have provided Pb with sufficiently radiogenic compositions that was added to less radiogenic Pb remobilised from precursor Cu-Pb-Zn-Fe polysulphides, whereas the U most likely originated from external sources. Local metal sources are also suggested by the 208Pb/204Pb-206Pb/204Pb systematics of combined ore and rock lead, which indicate a pronounced and diversified lithological control of the immediate host rocks on the chalcocite-dominated Cu-Ag ores. The Pb isotope systematics of polysulphide mineralisation on the Kundelungu Plateau clearly record a diachronous evolution.

  7. Fluids in distal Zn-Pb-Ag skarns: Evidence from El Mochito, Honduras

    NASA Astrophysics Data System (ADS)

    Samson, I. M.; Williams-Jones, A. E.; Ault, K.; Gagnon, J. E.; Fryer, B. J.

    2009-05-01

    Zn-Pb-Ag mantos, chimneys, and skarns represent a spectrum of carbonate-hosted sulfide mineral deposits that have been collectively termed carbonate replacement deposits. Most such deposits cannot be related to plutons and, particularly for distal skarns, the role of magmatic versus other fluids (basinal brines and meteoric waters) has been uncertain. The El Mochito Zn-Pb-Ag deposit, Honduras, is an example of a large distal skarn, and comprises mantos and chimneys hosted mainly by limestones of the Early Cretaceous Tepemechin Formation. Previous isotopic studies indicate a magmatic source for the S and Pb and involvement of both magmatic and meteoric fluids in ore formation. The ore is hosted by garnet, magnetite, and pyroxene skarns, which developed sequentially from grandite- to andradite- to magnetite- and hedenbergite- rich skarns. Sphalerite and argentiferous galena occur interstitially to, or replace, the skarn minerals, with Fe- poor sphalerite (S1) principally associated with garnet skarn and Fe-rich (S2) sphalerite associated with pyroxene. Data from primary fluid inclusions show that the salinity of the mineralizing fluids decreased from ˜10-18 wt. % during the formation of garnet skarn and S1 sphalerite to ˜2-13 wt. % during pyroxene skarn formation and S2 sphalerite precipitation. Early, high-salinity fluids (˜33 wt. %) are represented by rare halite-saturated inclusions in garnet. Temperature increased from ˜ 365°C to ˜ 365°C from garnet/S1 sphalerite to pyroxene/S2 sphalerite, assuming a pressure of 500 bars. GC analyses indicate that the total concentrations of COv(2), CH4, and N2 were < 1 mole %. LA-ICPMS analyses were conducted mainly on inclusions in grandite and S1 sphalerite. The principal dissolved elements in the inclusions are Ca and Na, followed by K and Mn. The ore metals, Zn, Pb, and Ag, are present in high concentrations, with median values of 6000, 900, and 50 ppm, respectively. Element concentrations in fluid inclusions hosted

  8. Relationship between the Porco, Bolivia, Ag-Zn-Pb-Sn deposit and the Porco Caldera

    USGS Publications Warehouse

    Cunningham, C.G.

    1994-01-01

    The Porco Ag-Zn-Pb-Sn deposit, a major Ag producer in the 16th century and currently the major Zn producer in Bolivia, consists of a swarm of fissure-filling veins in the newly recognized Porco caldera. The caldera measures 5 km by 3 km and formed in response to the eruption of the 12 Ma crystal-rich dacitic Porco Tuff. The mineralization is associated with, and is probably genetically related to, the 8.6 Ma Huayna Porco stock. The Porco deposit consists of steeply dipping irregular and curvilinear veins that cut the intracaldera Porco Tuff about 1 km east of the Huayna Porco stock. Most of the veins are aligned along the structural margin (ring fracture) of the caldera. The ore deposit is zoned around the Huayna Porco stock. The primary Ag minerals are most abundant in the upper parts of the viens. Fluid inclusions in sphalerite stalactites have homogenization temperatures of about 225??C and salinities of about 8 wt% NaCl equiv. The stalactites and the presence of sparse vapor-rich inclusions suggest deposition of sphalerite under boiling conditions. -from Authors

  9. Paleomagnetic Age for the World-class Century Zn-Pb-Ag Deposit, Australia

    NASA Astrophysics Data System (ADS)

    Kawasaki, K.; Symons, D. T.; Dawborn, T.

    2009-05-01

    Paleomagnetic results are reported for the Century Zn-Pb-Ag SEDEX deposit in northwestern Queensland, Australia. The stratiform mineralization occurs in fine parallel lamellae in ˜1595 Ma siderite-rich siltstones and black shales of the upper Lawn Hill Formation in the Proterozoic McNamara Group. Galena from the deposit has given a Pb/Pb model age of ˜1575 Ma. Paleomagnetic analysis of 333 specimens from ore zones (15 sites), and hanging wall (4 sites) and footwall (5 sites) siltstones using mostly thermal and then alternating field step demagnetization, isolates a stable characteristic remanent magnetization (ChRM) for the ore sites only. Step demagnetization, rock magnetic tests and thermomagnetic analyses of ore, Zn and Pb concentrates and tailings show that the main remanence carriers are single- or pseudosingle-domain inclusions of titanomagnetite in sphalerite and gangue, and pyrrhotite in galena with modern goethite and/or hematite from the weathering of siderite. A paleomagnetic fold test using the ore sites is positive, showing that the ore ChRM predates D2 deformation in the ˜1595 to ˜1500 Ma Isan orogeny. The orogeny folded the main-stage mineralization, indicating that the ore retains a primary magnetization. The optimum 80% tilt-corrected unit mean ChRM direction for the ore gives a Mesoproterozoic paleopole at ˜1560 Ma on the northern Australian apparent polar wander path. Thus this result both constrains the timing of mineralization and provides an upper age limit for D2 deformation in the orogeny.

  10. Sm-Nd dating of the giant Sullivan Pb-Zn-Ag deposit, British Columbia

    USGS Publications Warehouse

    Jiang, Shao-Yong; Slack, John F.; Palmer, Martin R.

    2000-01-01

    We report here Sm and Nd isotope data for hydrothermal tourmalinites and sulfide ores from the giant Sullivan Pb-Zn-Ag deposit, which occurs in the lower part of the Mesoproterozoic Purcell (Belt) Supergroup. Whole-rock samples of quartz-tourmaline tourmalinite from the footwall alteration pipe yield a Sm-Nd isochron age of 1470 ± 59 Ma, recording synsedimentary B metasomatism of clastic sediments during early evolution of the Sullivan hydrothermal system. Data for variably altered (chloritized and/or albitized) tourmalinites from the hanging wall of the deposit, which are believed to have formed originally ca. 1470 Ma, define a younger 1076 ± 77 Ma isochron because of resetting of Sm and Nd isotopes during Grenvillian metamorphism. HCl leachates of bedded Pb-Zn ore yield a Sm-Nd isochron age of 1451 ± 46 Ma, which is consistent with syngenetic-exhalative mineralization ca. 1470 Ma; this age could also reflect a slightly younger, epigenetic hydrothermal event. Results obtained for the Sullivan deposit indicate that the Sm-Nd geochronometer has the potential to directly date mineralization and alteration in stratabound sulfide deposits that are not amenable to dating by other isotope methods.

  11. Structure and age of the Cerro de Pasco Cu-Zn-Pb-Ag deposit, Peru

    NASA Astrophysics Data System (ADS)

    Cheney, E. S.

    1991-04-01

    The world-famous Cu-Zn-Pb-Ag deposit at Cerro de Pasco, Peru, consists of texturally massive pyrite, texturally massive sphalerite-galena-pyrite, and veins containing pyrite and enargite. Historically the deposit has been considered to be the hydrothermal product of the adjacent Miocene volcanic and intrusive complex (locally known as the “Vent”). However, both the texturally massive sulfides of the deposit and the pre-Miocene strata are cut by the Longitudinal fault, one of the largest faults in the district, but the Vent is not. Imbrication by the Longitudinal fault zone (duplex structures) has thickened the deposit so that it is amenable to open-pit mining. Dikes and pyrite-enargite veins pass from the Vent into the massive sulfides; fragments of massive pyrite occur in the Vent. Thus, no matter what their origin, the texturally massive sulfides are older and, therefore, genetically unrelated to the Vent.

  12. Fluid inclusions and isotopic characteristics of the Jiawula Pb-Zn-Ag deposit, Inner Mongolia, China

    NASA Astrophysics Data System (ADS)

    Li, Tiegang; Wu, Guang; Liu, Jun; Hu, Yanqing; Zhang, Yunfu; Luo, Dafeng; Mao, Zhihao

    2015-05-01

    The large Jiawula Pb-Zn-Ag deposit is located in the Derbugan metallogenic belt of the northern Great Xing'an Range. The vein style orebodies of the deposit occur along NWW- to NNW-trending fault zones. The ore-forming process at the deposit can be divided into three stages: an early quartz-pyrite-pyrrhotite-chalcopyrite stage, a middle quartz-carbonate-pyrite-galena-sphalerite stage, and a late quartz-carbonate-pyrite stage. Sulfide Rb-Sr dating indicates that the Jiawula deposit formed at ca. 143-142 Ma. Four types of fluid inclusions have been distinguished in quartz veins including liquid-rich, gas-rich, H2O-CO2, and daughter mineral-bearing inclusions. The fluid inclusions of the early stage are mainly liquid-rich, gas-rich, and H2O-CO2 types, with a small number containing daughter minerals. Cumulatively, the types have homogenization temperatures, densities, and salinities of 304-438 °C, 0.35-1.37 g/cm3, and 0.8-44.6 wt.% NaCl eqv., respectively. Inclusions of the middle stage are mainly liquid-rich and gas-rich types, with a small amount of H2O-CO2 and daughter mineral-bearing types; their homogenization temperatures, densities, and salinities vary from 242 °C to 297 °C, 0.71 to 1.44 g/cm3, and 0.4 wt.% to 36.8 wt.% NaCl eqv., respectively. The late stage only comprises liquid-rich inclusions with homogenization temperatures, densities, and salinities of 181-238 °C, 0.81-0.90 g/cm3, and 0.2-1.9 wt.% NaCl eqv., respectively. The ore-forming fluids of the Jiawula deposit are generally characterized by moderate temperature and low salinity and density, and belong to an H2O-NaCl-CO2 ± CH4 system. The δ18Owater values calculated for ore-bearing quartz vary from -13.4‰ to -9.1‰, and the δDV-SMOW values from bulk extraction of fluid inclusion waters vary from -166‰ to -133‰, suggesting that the ore-forming fluids mainly consist of meteoric water with a small amount of magmatic water. The δ34SV-CDT values range from 1.2‰ to 8.4‰. The 206Pb/204Pb

  13. Feruvite from the Sullivan Pb-Zn-Ag deposit, British Columbia

    USGS Publications Warehouse

    Jiang, S.-Y.; Palmer, M.R.; McDonald, A.M.; Slack, J.F.; Leitch, C.H.B.

    1996-01-01

    Feruvite, an uncommon Ca- and Fe2+-rich tourmaline species, has been discovered in the footwall of the Sullivan Pb-Zn-Ag deposit (British Columbia) near gabbro sills and dikes. Its chemical composition varies according to occurrence: feruvite from the shallow footwall has lower Ca, higher Al, and higher X-site vacancies than that from the deep footwall. The major chemical substitution involved in the feruvite is the exchange vector CaMgO???-1Al-1(OH)-1. The most important factor controlling feruvite formation at Sullivan is likely the reaction of Fe-rich hydrothermal fluids with Ca-rich minerals in gabbro and host rocks. This reaction led to the breakdown of Ca-rich minerals (plagioclase and hornblende), with release of Ca to solution and its incorporation into feruvite. This process probably postdated the main stages of formation of fine-grained, intermediate schorl-dravite in the tourmalinite pipe in the footwall, and is attributed to postore intrusion of gabbro and associated albite-chlorite-pyrite alteration.

  14. Alkali-deficient tourmaline from the Sullivan Pb-Zn-Ag deposit, British Columbia

    USGS Publications Warehouse

    Jiang, S.-Y.; Palmer, M.R.; Slack, J.F.

    1997-01-01

    Alkali-deficient tourmalines are found in albitized rocks from the hanging-wall of the Sullivan Pb-Zn-Ag deposit (British Columbia, Canada). They approximate the Mg-equivalent of foitite with an idealized formula D???(Mg2Al)Al6Si6O18(BO 3)3(OH)4. Major chemical substitutions in the tourmalines are the alkali-defect type [Na*(x) + Mg*(Y) = ???(X) + Al(Y)] and the uvite type [Na*(X) + Al(Y) = Ca(X) + Mg*(Y)], where Na* = Na + K, Mg* = Mg + Fe + Mn. The occurrence of these alkali-deficient tourmalines reflects a unique geochemical environment that is either alkali-depleted overall or one in which the alkalis preferentially partitioned into coexisting minerals (e.g. albite). Some of the alkali-deficient tourmalines have unusually high Mn contents (up to 1.5 wt.% MnO) compared to other Sullivan tourmalines. Manganese has a strong preference for incorporation into coexisting garnet and carbonate at Sullivan, thus many tourmalines in Mn-rich rocks are poor in Mn (<0.2 wt.% MnO). It appears that the dominant controls over the occurrence of Mn-rich tourmalines at Sullivan are the local availability of Mn and the lack of other coexisting minerals that may preferentially incorporate Mn into their structures.

  15. Testing WHAM-FTOX with laboratory toxicity data for mixtures of metals (Cu, Zn, Cd, Ag, Pb).

    PubMed

    Tipping, Edward; Lofts, Stephen

    2015-04-01

    The Windermere humic aqueous model using the toxicity function (WHAM-FTOX ) describes cation toxicity to aquatic organisms in terms of 1) accumulation by the organism of metabolically active protons and metals at reversible binding sites, and 2) differing toxic potencies of the bound cations. Cation accumulation (νi , in mol g(-1) ) is estimated through calculations with the WHAM chemical speciation model by assuming that organism binding sites can be represented by those of humic acid. Toxicity coefficients (αi ) are combined with νi to obtain the variable FTOX (= Σ αi νi ) which, between lower and upper thresholds (FTOX,LT , FTOX,UT ), is linearly related to toxic effect. Values of αi , FTOX,LT , and FTOX,LT are obtained by fitting toxicity data. Reasonable fits (72% of variance in toxic effect explained overall) were obtained for 4 large metal mixture acute toxicity experiments involving daphnids (Cu, Zn, Cd), lettuce (Cu, Zn, Ag), and trout (Zn, Cd, Pb). Strong nonadditive effects, most apparent in results for tests involving Cd, could be explained approximately by purely chemical competition for metal accumulation. Tentative interpretation of parameter values obtained from these and other experimental data suggests the following order of bound cation toxicity: H < Al < (Cu Zn Pb UO2 ) < (Cd Ag). Another trend is a strong increase in Cd toxicity relative to that of Zn as organism complexity increases (from bacteria to fish).

  16. Geology and origin of Ag-Pb-Zn deposits occurring in the Ulaan-Jiawula metallogenic province, northeast Asia

    NASA Astrophysics Data System (ADS)

    Nie, Feng-jun; Li, Qiang-feng; Liu, Chun-hua; Ding, Cheng-wu

    2015-01-01

    Located at the conjunction area of China, Mongolia and Russia in NE Asia, the Ulaan-Jiawula (also referred as UJ) region, with an area of 400,000 km2, is one of the most important Ag-Pb-Zn, U, Sn, W, Nb-Ta, and Au metallogenic provinces in Asia. At present, 2126 deposits and showings including 500 Ag-Pb-Zn deposits have been discovered, explored and mined since the late 1960s. These Ag-Pb-Zn occurrences can be subdivided into three types according to their geological setting, texture, alteration and mineral assemblages: (1) low sulfidation epithermal Ag-Pb-Zn deposits; (2) intermediate sulfidation epithermal Ag-Pb-Zn deposits; (3) mixed-type Ag-Pb-Zn deposit consisting of vein-like and tabular ore bodies. The Eren Tologoi and Tsagenbulagen deposits are representative of low-sulphidation type Ag-Pb-Zn mineralization in the UJ region, and are associated with intensive adularization and sericitization. Ore occurs as mineralized quartz veins, veinlet groups and altered-fracture zones within Mesozoic alkaline and high-K calc-alkaline volcanic rocks, Ore mineralogy includes native silver, electrum, pyrite, galena, sphalerite, arsenopyrite, pyrargyrite and chalcopyrite. The Tsav and Jiawula deposits are typical of intermediate sulfidation Ag-Pb-Zn mineralization. The δ34S value of sulfide (pyrite and galena) separates from groups 1 and 2 varies from 1.5‰ to 3.5‰ and 2.0‰ to 4.5‰, respectively. The δ34S values of the Mesozoic volcanic host rocks for groups 1 and 2 deposits also show the positive δ34S values of 1.5-4.8‰, while the δ34S value of pyrite separate from the pre-Jurassic schist range from -6‰ to -8‰ which are much lower than Mesozoic volcanic host rocks and their associated ore deposits. There is no difference between the δ34S value of sulfide (pyrite and galena) separates from vein-like ore bodies of the group 3 deposits and their wall rocks, having δ34S value of 1.0-5.0‰ and 1.2-4.5‰ which are similar to that of groups 1 and 2 deposits

  17. Re-Os and U-Pb geochronology of the Laochang Pb-Zn-Ag and concealed porphyry Mo mineralization along the Changning-Menglian suture, SW China: implications for ore genesis and porphyry Cu-Mo exploration

    NASA Astrophysics Data System (ADS)

    Deng, Xiao-Dong; Li, Jian-Wei; Zhao, Xin-Fu; Wang, Hong-Qiang; Qi, Liang

    2016-02-01

    Numerous polymetallic volcanogenic massive sulfide (VMS), vein, and replacement deposits are distributed along the Changning-Menglian suture zone in Sanjiang Tethyan metallogenic province, SW China. Laochang is the largest Pb-Zn-Ag vein and replacement deposit in this area, with a proven reserve of 0.51 Mt Pb, 0.34 Mt Zn, and 1,737 t Ag. Its age and relationship to magmatic events and VMS deposits in the region, however, have long been debated. In this paper, we present pyrite Re-Os and titanite U-Pb ages aiming to provide significant insights into the timing and genesis of the Pb-Zn-Ag mineralization. Pyrite grains in textural equilibrium with galena, sphalerite, and chalcopyrite from stratabound Pb-Zn-Ag and Cu-bearing Pb-Zn-Ag orebodies have a Re-Os isochron age of 45.7 ± 3.1 Ma (2 σ, mean square weighted deviation (MSWD) = 0.45), whereas titanite grains intergrown with sulfide minerals yield a weighted mean 206Pb/238U age of 43.4 ± 1.2 Ma (2 σ, n = 8). A Mo-mineralized granitic porphyry intersected by recent drilling below the Laochang Pb-Zn-Ag ores yields a zircon U-Pb age of 44.4 ± 0.4 Ma (2 σ, n = 12). Within analytical uncertainties, the ages of the Pb-Zn-Ag deposit and the concealed Mo-mineralized porphyry are indistinguishable, indicating that they are products of a single magmatic hydrothermal system. The results show that Laochang Pb-Zn-Ag deposit is significantly younger than the host mafic volcanic rock (zircon U-Pb age of 320.8 ± 2.7 Ma; 2 σ, n = 12) and Silurian VMS deposits along the Changning-Menglian suture zone, arguing against its origin as a Carboniferous VMS deposit as many researchers claimed. The initial 187Os/188Os ratio (0.540 ± 0.012) obtained from the pyrite Re-Os isochron suggests that metals were likely derived from the granitic porphyry that formed from a hybrid magma due to mixing of crustal- and mantle-derived melts, rather than from the mafic volcanic host rocks as previously thought. Our results favor that the Laochang

  18. Reactive flow models of the Anarraaq Zn-Pb-Ag deposit, Red Dog district, Alaska

    USGS Publications Warehouse

    Schardt, C.; Garven, G.; Kelley, K.D.; Leach, D.L.

    2008-01-01

    The Red Dog ore deposit district in the Brooks Range of northern Alaska is host to several high-grade, shale-hosted Zn + Pb deposits. Due to the complex history and deformation of these ore deposits, the geological and hydrological conditions at the time of formation are poorly understood. Using geological observations and fluid inclusion data as constraints, numerical heat and fluid flow simulations of the Anarraaq ore deposit environment and coupled reactive flow simulations of a section of the ore body were conducted to gain more insight into the conditions of ore body formation. Results suggest that the ore body and associated base metal zonation may have formed by the mixing of oxidized, saline, metal-bearing hydrothermal fluids (<200??C) with reducing, HS-rich pore fluids within radiolarite-rich host rocks. Sphalerite and galena concentrations and base metal sulfide distribution are primarily controlled by the nature of the pore fluids, i.e., the extent and duration of the HS- source. Forward modeling results also predict the distribution of pyrite and quartz in agreement with field observations and indicate a reaction front moving from the initial mixing interface into the radiolarite rocks. Heuristic mass calculations suggest that ore grades and base metal accumulation comparable to those found in the field (18% Zn, 5% Pb) are predicted to be reached after about 0.3 My for initial conditions (30 ppm Zn, 3 ppm Pb; 20% deposition efficiency). ?? Springer-Verlag 2008.

  19. Reactive flow models of the Anarraaq Zn-Pb-Ag deposit, Red Dog district, Alaska

    NASA Astrophysics Data System (ADS)

    Schardt, Christian; Garven, Grant; Kelley, Karen D.; Leach, David L.

    2008-09-01

    The Red Dog ore deposit district in the Brooks Range of northern Alaska is host to several high-grade, shale-hosted Zn + Pb deposits. Due to the complex history and deformation of these ore deposits, the geological and hydrological conditions at the time of formation are poorly understood. Using geological observations and fluid inclusion data as constraints, numerical heat and fluid flow simulations of the Anarraaq ore deposit environment and coupled reactive flow simulations of a section of the ore body were conducted to gain more insight into the conditions of ore body formation. Results suggest that the ore body and associated base metal zonation may have formed by the mixing of oxidized, saline, metal-bearing hydrothermal fluids (<200°C) with reducing, HS-rich pore fluids within radiolarite-rich host rocks. Sphalerite and galena concentrations and base metal sulfide distribution are primarily controlled by the nature of the pore fluids, i.e., the extent and duration of the HS- source. Forward modeling results also predict the distribution of pyrite and quartz in agreement with field observations and indicate a reaction front moving from the initial mixing interface into the radiolarite rocks. Heuristic mass calculations suggest that ore grades and base metal accumulation comparable to those found in the field (18% Zn, 5% Pb) are predicted to be reached after about 0.3 My for initial conditions (30 ppm Zn, 3 ppm Pb; 20% deposition efficiency).

  20. The geology of the carbonate-hosted Blende Ag-Pb-Zn deposit, Wernecke Mountains, Yukon, Canada

    NASA Astrophysics Data System (ADS)

    Moroskat, Micheal; Gleeson, Sarah A.; Sharp, R. J.; Simonetti, A.; Gallagher, C. J.

    2015-01-01

    The Ag-Zn-Pb Blende deposit is located in the Wernecke Mountains, Yukon and is hosted by the middle Proterozoic Gillespie Lake Group dolomitic siltstones. The sulphide mineralization is localized within the axial planar cleavage of a kilometre-scale anticline and is dominated by galena- and sphalerite-cemented mosaic, rubble and crackle breccias with minor pyrite, galena, sphalerite and dolomite veins. 206Pb/204Pb values from galena range from 16.355 to 16.600, 207Pb/204Pb from 15.430 to 15.461, and 208Pb/204Pb from 36.016 to 36.283, respectively, and yield model ages between 1,490 and 1,430 Ma. A hydrothermal alteration zone, which is younger than the mineralization, has a poorly constrained U-Pb monazite age of 1,307 ± 180 Ma, which suggests that the Blende deposit is Proterozoic in age. Dolomites associated with the main- and late-stage mineralization have δ13C values that range from -1.8 to 0.9 ‰ and δ18O values of 15.7 to 21.9 ‰. The total range of δ34S values from pyrite, galena and sphalerite is 9.4 to 58.1 ‰, indicating that the sulphur in the deposit was derived from reduction of seawater sulphate in a closed system. Strontium isotopes suggest there were three fluids involved in the Blende mineralizing system: Fluid 1 was derived from seawater and formed carbonate and quartz veins pre-mineralization; it has an 87Sr/86Sr ratio of 0.70948. Fluid 2 has a high 87Sr/86Sr ratio of 0.73866, and fluid 3 has a Sr isotopic ratio of 0.71602. Fluids 1 and 3 have similar isotopic compositions but different total Sr ion signals (a function of concentration). This suggests that fluids 1 and 3 may have ultimately been derived from Proterozoic seawater but have undergone different amounts of water-rock interaction. The isotopic and geochemical data suggest the mineralization formed when a H2S-rich fluid derived from seawater (fluid 3) mixed with a metal-bearing fluid (fluid 2) in the high permeability zones of the axial planar cleavage. The Blende deposit is an

  1. Origin of the Red Dog Zn-Pb-Ag deposits, Brooks Range, Alaska: Evidence from regional Pb and Sr isotope sources

    USGS Publications Warehouse

    Ayuso, R.A.; Kelley, K.D.; Leach, D.L.; Young, L.E.; Slack, J.F.; Wandless, G.; Lyon, A.M.; Dillingham, J.L.

    2004-01-01

    Pb and Sr isotope data were obtained on the shale-hosted Zn-Pb-Ag Red Dog deposits (Qanaiyaq, Main, Aqqaluk, and Paalaaq), other shale-hosted deposits near Red Dog, and Zn-Pb-Ag sulfide and barite deposits in the western and central Brooks Range. The Red Dog deposits and other shale-hosted Zn-Pb-Ag deposits near Red Dog are hosted in the Mississippian Kuna Formation, which is underlain by a sequence of marine-deltaic clastic rocks of the Upper Devonian to Lower Mississippian Endicott Group. Ag-Pb-Zn vein-breccias are found in the Endicott Group. Galena formed during the main mineralization stages in the Red Dog deposits and from the Anarraaq and Wulik deposits have overlapping Pb isotope compositions in the range 206Pb/204Pb = 18.364 to 18.428, 207Pb/204Pb = 15.553 to 15.621, and 208Pb/204Pb = 38.083 to 38.323. Galena and sphalerite formed during the main ore-forming stages in the Red Dog deposits define a narrow field on standard uranogenic and thorogenic Pb isotope diagrams. Lead in sulfides of the Red Dog district is less radiogenic (238U/204Pb: ?? = 9.51-9.77) than is indicated by the average crustal lead evolution model (?? = 9.74), a difference consistent with a long history of evolution at low ratios of ?? before the Carboniferous. The homogeneous regional isotopic reservoir of Pb may indicate large-scale transport and leaching of minerals with various ?? ratios and Th/Pb ratios. Younger and genetically unrelated fluids did not significantly disturb the isotopic compositions of galena and sphalerite after the main mineralization event in the Red Dog district. Some pyrite shows evidence of minor Pb remobilization. The overall lead isotope homogeneity in the shale-hosted massive sulfide deposits is consistent with three types of control: a homogeneous regional source, mixing of lead during leaching of a thick sedimentary section and fluid transport, or mixing at the site of deposition. Isotopic variability of the hydrothermal fluids, as represented by galena

  2. Mineral chemistry and shrimp U-Pb Geochronology of mesoproterozoic polycrase-titanite veins in the sullivan Pb-Zn-Ag Deposit, British Columbia

    USGS Publications Warehouse

    Slack, J.F.; Aleinikoff, J.N.; Belkin, H.E.; Fanning, C.M.; Ransom, P.W.

    2008-01-01

    Small polycrase-titanite veins 0.1-2 mm thick cut the tourmalinite feeder zone in the deep footwall of the Sullivan Pb-Zn-Ag deposit, southeastern British Columbia. Unaltered, euhedral crystals of polycrase and titanite 50-100 ??m in diameter are variably replaced by a finer-grained alteration-induced assemblage composed of anhedral polycrase and titanite with local calcite, albite, epidote, allanite, and thorite or uranothorite (or both). Average compositions of the unaltered and altered polycrase, as determined by electron-microprobe analysis, are (Y0.38 REE0.49 Th0.10 Ca0.04 Pb0.03 Fe0.01U0.01) (Ti1.48 Nb0.54 W0.04 Ta0.02)O6 and (Y0.42 REE0.32 Th0.15 U0.06 Ca0.04 Pb0.01 Fe0.01) (Ti1.57 Nb0.44 W0.04 Ta0.02)O6, respectively. The unaltered titanite has, in some areas, appreciable F (to 0.15 apfu), Y (to 0.40 apfu), and Nb (to 0.13 apfu). SHRIMP U-Pb geochronology of eight grains of unaltered polycrase yields a weighted 207Pb/206Pb age of 1413 ?? 4 Ma (2??) that is interpreted to be the age of vein formation. This age is 50-60 m.y. younger than the ca. 1470 Ma age of synsedimentary Pb-Zn-Ag mineralization in the Sullivan deposit, which is based on combined geological and geochronological data. SHRIMP ages for altered polycrase and titanite suggest later growth of minerals during the ???1370-1320 Ma East Kootenay and ???1150-1050 Ma Grenvillian orogenies. The 1413 ?? 4 Ma age for the unaltered polycrase in the veins records a previously unrecognized post-ore (1370 Ma) mineralizing event in the Sullivan deposit and vicinity. The SHRIMP U-Pb age of the polycrase and high concentrations of REE, Y, Ti, Nb, and Th in the veins, together with elevated F in titanite and the absence of associated sulfides, suggest transport of these high-field-strength elements (HFSE) by F-rich and S-poor hydrothermal fluids unrelated to the fluids that formed the older Fe-Pb-Zn-Ag sulfide ores of the Sullivan deposit. Fluids containing abundant REE, HFSE, and F may have been derived from a

  3. Geochronology, fluid inclusions and isotopic characteristics of the Chaganbulagen Pb-Zn-Ag deposit, Inner Mongolia, China

    NASA Astrophysics Data System (ADS)

    Li, Tiegang; Wu, Guang; Liu, Jun; Wang, Guorui; Hu, Yanqing; Zhang, Yunfu; Luo, Dafeng; Mao, Zhihao; Xu, Bei

    2016-09-01

    The large Chaganbulagen Pb-Zn-Ag deposit is located in the Derbugan metallogenic belt of the northern Great Xing'an Range. The vein-style orebodies of the deposit occur in the NWW-trending fault zones. The ore-forming process at the deposit can be divided into three stages: an early quartz-pyrite-arsenopyrite-pyrrhotite-sphalerite-galena-chalcopyrite stage, a middle quartz-carbonate-pyrite-sphalerite-galena-silver-bearing minerals stage, and a late quartz-carbonate-pyrite stage. The sericite sample yielded a 40Ar -39Ar plateau age of 138 ± 1 Ma and an isochron age of 137 ± 3 Ma, and the zircon LA-ICP-MS U-Pb age of monzogranite porphyry was 143 ± 2 Ma, indicating that the ages of mineralization and monzogranite porphyry in the Chaganbulagen deposit should be the Early Cretaceous, and that the mineralization should be slightly later than the intrusion of monzogranite porphyry. There are only liquid inclusions in quartz veins of the Chaganbulagen deposit. Homogenization temperatures, densities, and salinities of the fluid inclusions from the early stage are 261-340 °C, 0.65-0.81 g/cm3, and 0.7-6.3 wt.% NaCl eqv., respectively. Fluid inclusions of the middle stage have homogenization temperatures, densities, and salinities of 209-265 °C, 0.75-0.86 g/cm3, and 0.5-5.7 wt.% NaCl eqv., respectively. For fluid inclusions of the late stage, their homogenization temperatures, densities, and salinities are 173-219 °C, 0.85-0.91 g/cm3, and 0.4-2.7 wt.% NaCl eqv., respectively. The ore-forming fluids of the deposit are generally characterized by moderate temperature and low salinity and density, and belong to an H2O-NaCl ± CO2 ± CH4 system. The δ18Owater values calculated for ore-bearing quartz vary from - 17.9‰ to - 10.8‰, and the δDV-SMOW values from bulk extraction of fluid inclusion waters vary from - 166‰ to - 127‰, suggesting that the ore-forming fluids consist dominantly of meteoric water. The δ34SV-CDT values range from 1.4‰ to 4.1‰. The 206Pb/204

  4. The Anarraaq Zn-Pb-Ag and barite deposit, northern Alaska: Evidence for replacement of carbonate by barite and sulfides

    USGS Publications Warehouse

    Kelley, K.D.; Dumoulin, J.A.; Jennings, S.

    2004-01-01

    The Anarraaq deposit in northern Alaska consists of a barite body, estimated to be as much as 1 billion metric tons, and a Zn-Pb-Ag massive sulfide zone with an estimated resource of about 18 Mt at 18 percent Zn, 5.4 percent Pb, and 85 g/t Ag. The barite and sulfide minerals are hosted by the uppermost part of the Mississippian Kuna Formation (Ikalukrok unit) that consists of carbonaceous and siliceous mudstone or shale interbedded with carbonate. The amount of interbedded carbonate in the Anarraaq deposit is atypical of the district as a whole, comprising as much as one third of the section. The total thickness of the Ikalukrok unit is considerably greater in the area of the deposit (210 to almost 350 m) than to the north and south (maximum of 164 m). The mineralized zone at Anarraaq is lens shaped and has a relatively flat top and a convex base. It also ranges greatly in thickness, from a few meters to more than 100 m. Textures of some of the carbonate layers are distinctive, consisting of nodules within siliceous mudstone or layers interbedded with shale. Many of the layers contain calcitized sponge spicules or radiolarians in a carbonate matrix. Textures of barite and sulfide minerals mimic those of carbonate and provide unequivocal evidence that replacement of precursor carbonate was an important process. Barite and sulfide textures include either nodular, bladed grains of various sizes that resemble spicules (observed only with iron sulfides) or well-rounded forms that are replaced radiolarians. Mineralization at Anarraaq probably occurred in a fault-bounded Carboniferous basin during early diagenesis in the shallow subsurface. The shape and size of the mineralized body suggest that barite and sulfides replaced calcareous mass flow deposits in a submarine channel. The distribution of biogenic and/or early diagenetic silica may have served as impermeable barriers to the fluids, thereby focusing and controlling fluid flow through unreplaced carbonate layers

  5. Origin of epithermal Ag-Au-Cu-Pb-Zn mineralization in Guanajuato, Mexico

    NASA Astrophysics Data System (ADS)

    Mango, Helen; Arehart, Greg; Oreskes, Naomi; Zantop, Half

    2014-01-01

    The Guanajuato epithermal district is one of the largest silver producers in Mexico. Mineralization occurs along three main vein systems trending dominantly northwest-southeast: the central Veta Madre, the La Luz system to the northwest, and the Sierra system to the east. Mineralization consists dominantly of silver sulfides and sulfosalts, base metal sulfides (mostly chalcopyrite, galena, sphalerite, and pyrite), and electrum. There is a broad zonation of metal distribution, with up to 10 % Cu+Pb+Zn in the deeper mines along the northern and central portions of the Veta Madre. Ore occurs in banded veins and breccias and as stockworks, with gangue composed dominantly of quartz and calcite. Host rocks are Mesozoic sedimentary and intrusive igneous rocks and Tertiary volcanic rocks. Most fluid inclusion homogenization temperatures are between 200 and 300 °C, with salinities below 4 wt.% NaCl equivalent. Fluid temperature and salinity decreased with time, from 290 to 240 °C and from 2.5 to 1.1 wt.% NaCl equivalent. Relatively constant fluid inclusion liquid-to-vapor ratios and a trend of decreasing salinity with decreasing temperature and with increasing time suggest dilution of the hydrothermal solutions. However, evidence of boiling (such as quartz and calcite textures and the presence of adularia) is noted along the Veta Madre, particularly at higher elevations. Fluid inclusion and mineralogical evidence for boiling of metal-bearing solutions is found in gold-rich portions of the eastern Sierra system; this part of the system is interpreted as the least eroded part of the district. Oxygen, carbon, and sulfur isotope analysis of host rocks, ore, and gangue minerals and fluid inclusion contents indicate a hydrothermal fluid, with an initial magmatic component that mixed over time with infiltrating meteoric water and underwent exchange with host rocks. Mineral deposition was a result of decreasing activities of sulfur and oxygen, decreasing temperature, increasing p

  6. Geological, fluid inclusion and isotopic studies of the Yinshan Cu-Au-Pb-Zn-Ag deposit, South China: Implications for ore genesis and exploration

    NASA Astrophysics Data System (ADS)

    Wang, Guo-Guang; Ni, Pei; Wang, Ru-Cheng; Zhao, Kui-Dong; Chen, Hui; Ding, Jun-Ying; Zhao, Chao; Cai, Yi-Tao

    2013-09-01

    The Yinshan Cu-Au-Pb-Zn-Ag deposit is located in Dexing, South China. Ore bodies are primarily hosted in low-grade phyllite of the Neoproterozoic Shuangqiaoshan Group along EW- and NNW-striking fault zones. Pb-Zn-Ag mineralization is dictated by Jurassic rhyolitic quartz porphyries (ca. 172 Ma), whereas Cu-Au mineralization is associated with Jurassic dacite porphyries (ca. 170 Ma). The main ore minerals are pyrite, chalcopyrite, galena, sphalerite, tetrahedrite-tennatite, gold, silver, and silver sulphosalt, and the principal gangue minerals are quartz, sericite, calcite, and chlorite. Two-phase liquid-rich (type I), two-phase vapor-rich (type II), and halite-bearing (type III) fluid inclusions can be observed in the hydrothermal quartz-sulfides veins. Type I inclusions are widespread and have homogenization temperatures of 187-303 °C and salinities of 4.2-9.5 wt.% NaCl equivalent in the Pb-Zn-Ag mineralization, and homogenization temperatures of 196-362 °C and salinities of 3.5-9.9 wt.% NaCl equivalent in the Cu-Au mineralization. The pervasive occurrence of type I fluid inclusions with low-moderate temperatures and salinities implies that the mineralizing fluids formed in epithermal environments. The type II and coexisting type III inclusions, from deeper levels below the Cu-Au ore bodies, share similar homogenization temperatures of 317-448 °C and contrasting salinities of 0.2-4.2 and 30.9-36.8 wt.% NaCl equivalent, respectively, which indicates that boiling processes occurred. The sulfur isotopic compositions of sulfides (δ34S = -1.7‰ to +3.2‰) suggest a homogeneous magmatic sulfur source. The lead isotopes of sulfides (206Pb/204Pb = 18.01-18.07; 207Pb/204Pb = 15.55-15.57; and 208Pb/204Pb = 38.03-38.12) are consistent with those of volcanic-subvolcanic rocks (206Pb/204Pb = 18.03-18.10; 207Pb/204Pb = 15.56-15.57; and 208Pb/204Pb = 38.02-38.21), indicating a magmatic origin for lead in the ore. The oxygen and hydrogen isotope compositions (δ18O = +7.8

  7. Multistage hydrothermal silicification and Fe-Tl-As-Sb-Ge-REE enrichment in the Red Dog Zn-Pb-Ag district, northern Alaska: Geochemistry, origin, and exploration applications

    USGS Publications Warehouse

    Slack, J.F.; Kelley, K.D.; Anderson, V.M.; Clark, J.L.; Ayuso, R.A.

    2004-01-01

    Geochemical analyses of major, trace, and rare earth elements (REE) in more than 200 samples of variably silicified and altered wall rocks, massive and banded sulfide, silica rock, and sulfide-rich and unmineralized barite were obtained from the Main, Aqqaluk, and Anarraaq deposits in the Red Dog Zn-Pb-Ag district of northern Alaska. Detailed lithogeochemical profiles for two drill cores at Aqqaluk display an antithetic relationship between SiO2/Al2O3 and TiO2/Zr which, together with textural information, suggest preferential silicification of carbonate-bearing sediments. Data for both drill cores also show generally high Tl, Sb, As, and Ge and uniformly positive Eu anomalies (Eu/Eu* > 1.0). Similar high Tl, Sb, As, Ge, and Eu/Eu* values are present in the footwall and shallow hanging wall of Zn-Pb-Ag sulfide intervals at Anarraaq but are not as widely dispersed. Net chemical changes for altered wall rocks in the district, on the basis of average Al-normalized data relative to unaltered black shales of the host Kuna Formation, include large enrichments (>50%) of Fe, Ba, Eu, V, S, Co, Zn, Pb, Tl, As, Sb, and Ge at both Red Dog and Anarraaq, Si at Red Dog, and Sr, U, and Se at Anarraaq. Large depletions (>50%) are evident for Ca at both Red Dog and Anarraaq, for Mg, P, and Y at Red Dog, and for Na at Anarraaq. At both Red Dog and Anarraaq, wall-rock alteration removed calcite and minor dolomite during hydrothermal decarbonation reactions and introduced Si, Eu, and Ge during silicification. Sulfidation reactions deposited Fe, S, Co, Zn, Pb, Tl, As, and Sb; barite mineralization introduced Ba, S, and Sr. Light REE and U were mobilized locally. This alteration and mineralization occurred during Mississippi an hydrothermal events that predated the Middle Jurassic-Cretaceous Brookian orogeny. Early hydrothermal silicification at Red Dog took place prior to or during massive sulfide mineralization, on the basis of the dominantly planar nature of Zn-Pb veins, which suggests

  8. Paragenesis and chemistry of multistage tourmaline formation in the sullivan Pb-Zn-Ag deposit, British Columbia

    USGS Publications Warehouse

    Jiang, S.-Y.; Palmer, M.R.; Slack, J.F.; Shaw, D.R.

    1998-01-01

    Detailed petrographic study, scanning electron microscope imaging, and electron microprobe analyses of tourmalines from the Sullivan Pb-Zn-Ag massive sulfide deposit (British Columbia, Canada) document multiple paragenetic stages and large compositional variations. The tourmalines mainly belong to two common solid-solution series: dravite-schorl and dravite-uvite. Ca- and Fe-rich feruvite and alkali-deficient tourmalines are present locally. Products of tourmaline-forming stages include (from oldest to youngest): (1) rare Fe-rich dravite-schorl within black tourmalinite clasts in footwall fragmental rocks; (2) widespread Mg-rich, very fine grained, felted dravite in the footwall (the main type of tourmaline in the footwall tourmalinite pipe); (3) recrystallized, Fe-rich dravite-schorl (locally Ca-Fe feruvite) in the tourmalinite pipe, which preferentially occurs near postore gabbroic intrusions; (4) Mg-rich dravite or uvite associated with chlorite-pyrrhotite and chlorite-albite-pyrite-altered rocks in the shallow footwall and hanging wall; (5) discrete Mg-rich tourmaline grains associated with chlorite and discordant Mg-rich tourmaline rims which occur on disseminated Fe-rich schorl in the bedded Pb-Zn-Ag ores. The timing of rare Fe-rich schorl in the bedded ores is uncertain, but it most likely occurred during or between stages 2 and 3. The different paragenetic stages and their respective tourmaline compositions are interpreted in terms of a multistage evolution involving contributions from: (1) variable mixtures of synsedimentary, Fe-rich hydrothermal fluids and entrained seawater; (2) postore, Fe-rich, gabbro-related hydrothermal fluids; and (3) postore metamorphic reactions. Early synsedimentary, Fe-rich hydrothermal fluids which contained little or no entrained seawater formed Fe-rich black tourmalinite clasts locally in the footwall. The major type of tourmaline in the footwall tourmalinite pipe is Mg rich, recording seawater entrainment under high water

  9. Mineralogical and isotopic studies of base metal sulfides from the Jiawula Ag-Pb-Zn deposit, Inner Mongolia, NE China

    NASA Astrophysics Data System (ADS)

    Niu, Si-Da; Li, Sheng-Rong; Santosh, M.; Zhang, De-Hui; Li, Zeng-Da; Shan, Meng-Jie; Lan, Yi-Xiang; Gao, De-Rong; Zhao, Wen-Bin

    2016-01-01

    The Jiawula Ag-Pb-Zn deposit is located in the northern part of the Da Hinggan Mountains metallogenic belt in the eastern section of the Central Asian Orogenic Belt. Sphalerite, galena, pyrite, chalcopyrite, and arsenopyrite are the major sulfide minerals occurring in this deposit. Here we report results from electron probe micro-analysis (EPMA), thermoelectricity, and sulfur isotope studies of the constituent silver minerals and sulfide phases of the Jiawula deposit. Petrographic observations and EPMA study reveal abundant silver mineralization in the ore, especially within sphalerite and galena. Discrete grains of silver minerals (including argentite, pyrargyrite, and canfieldite) and isomorphism in silver-bearing sulfides are identified. Silver and tellurium contents in galena are relatively high and show interrelationship. Significant substitution of S by Te in the galena lattice facilitates silver entering the galena structure, which might have been promoted by relatively low lg fS2. The thermoelectric coefficient of pyrite shows a marked gradient from N-type to P-type from pre- to post-metallogenic stages. Pyrites in Jiawula are enriched in Co and As and in the absence of Ni, displaying features typical of epithermal deposits. The isotopic data present a close relationship between the sulfur source and magmatism.

  10. Mesozoic magmatism and timing of epigenetic Pb-Zn-Ag mineralization in the western Fortymile mining district, east-central Alaska: Zircon U-Pb geochronology, whole-rock geochemistry, and Pb isotopes

    USGS Publications Warehouse

    Dusel-Bacon, Cynthia; Aleinkoff, J.N.; Day, W.C.; Mortensen, J.K.

    2015-01-01

    Epigenetic Pb-Zn-Ag ± Cu prospects in the western Fortymile district are spatially associated with splays of the northeast-trending Kechumstuk sinistral-normal fault zone and with ca. 68-66 Ma felsic intrusions and dikes. The similarity between Pb isotope compositions of feldspars from the Late Cretaceous igneous bodies and sulfides from the epithermal prospects suggests a Late Cretaceous age for most of the mineralization. Fluid flow along the faults undoubtedly played a major role in mineralization. We interpret displacement on the northeast-trending faults to be a far-field effect of dextral translation along Late Cretaceous plate-scale boundaries and faults that were roughly parallel to the subsequently developed Denali and Tintina fault systems, which currently bound the region.

  11. Three mechanisms of ore re-mobilisation during amphibolite facies metamorphism at the Montauban Zn-Pb-Au-Ag deposit

    NASA Astrophysics Data System (ADS)

    Tomkins, Andrew G.

    2007-08-01

    The relative importance of mechanical re-mobilisation, hydrothermal dissolution and re-precipitation, and sulphide melting in controlling redistribution of metals during concurrent metamorphism and deformation is evaluated at the middle amphibolite facies Montauban deposit in Canada. As at many other deposits, ductile deformation was important in driving mechanical re-mobilisation of massive sulphides from limb regions into hinge regions of large-scale folds and is thus the most important for controlling the economics of Pb and Zn distribution. Two possible stages of hydrothermally driven re-mobilisation are discussed, each of which produces characteristically different alteration assemblages. Prograde hydrothermal re-mobilisation is driven by pyrite de-sulphidation and concurrent chlorite dehydration and is thus an internally driven process. At Montauban, the H2S-rich fluid generated through this process allowed re-mobilisation of gold into the wall rock, where it was deposited in response to sulphidation of Fe Mg silicates. Retrograde hydrothermal re-mobilisation is an externally driven process, whereby large volumes of fluids from outside the deposit may dissolve and re-precipitate metals, and cause hydration of silicate minerals. This second hydrothermally driven process is not recognised at Montauban. Sulphide melting occurred as temperatures neared the peak metamorphic conditions. Melting initiated in the massive sulphides through arsenopyrite breakdown, and a small volume of melt was subsequently re-mobilised into the wall rock. Trace element partitioning and fractional crystallisation of this melt generated a precious metal-rich fractionate, which remained mobile until well after peak metamorphism. Thus, prograde hydrothermal re-mobilisation and sulphide melting were the most important mechanisms for controlling the distribution of Au and Ag.

  12. Boron isotope systematics of tourmaline formation in the Sullivan Pb-Zn-Ag deposit, British Columbia, Canada

    USGS Publications Warehouse

    Jiang, S.-Y.; Palmer, M.R.; Slack, J.F.; Shaw, D.R.

    1999-01-01

    We report here the results of 54 boron isotope analyses of tourmaline associated with the giant Sullivan Pb-Zn-Ag deposit in southeastern British Columbia, Canada. The ??11B values range from -11.1 to -2.9???, which is almost as great as the range found worldwide in tourmalines from 33 massive sulfide deposits and tourmalinites in dominantly clastic metasedimentary terranes. The major control on the overall ??11B values of the Sullivan tourmalinites is the boron source. Potential controls over the large range of the data also include: (1) differences in formation temperatures of the tourmalinites, (2) different stages of tourmaline formation, (3) variations in the proportions of dissolved boron incorporated into the tourmaline (Rayleigh fractionation), (4) seawater entrainment, and (5) post-depositional metamorphism. The boron isotope data at Sullivan are consistent with boron derivation from leaching of footwall clastic sediments. However, the great abundance of tourmaline in the Sullivan deposit suggests that the local clastic sediments were not the sole source of boron, and we argue that non-marine evaporites, buried deep below the orebody, are the most viable source of this additional boron. It is likely that some of the variation in tourmaline ??11B values reflect mixing of boron from these two sources. Comparison of the potential effects of these controls with geologic and other geochemical evidence suggests that major causes for the wide range of ??11B values measured at Sullivan are seawater entrainment and Rayleigh fractionation, although in places, post-depositional alteration and thermal metamorphism were important in determining ??11B values of some of the recrystallized tourmalinites.

  13. Geochronology of the western and central Brooks Range, Alaska: Implications for the geologic evolution of the Anarraaq and Red Dog Zn-Pb-Ag deposits

    USGS Publications Warehouse

    Rombach, C.S.; Layer, P.W.

    2004-01-01

    A compilation of published geochronology of rocks and minerals from the western and central Brooks Range provides a framework for understanding the complex history of the Brooks Range and northern Alaska. A simplified timeline of events comprises (1) Devonian extension, (2) Mississippian extension and Zn-Pb-Ag mineralization, (3) a passive interval, (4) pre-Brooks Range orogeny rock-formation and thermal event, (5) inception of Brooks Range orogeny, (6) exhumation and the end of main-stage deformation, and (7) subsequent episodic deformation. This compilation is supplemented by new 40Ar/39Ar dates of white mica from the Anarraaq and Red Dog Zn-Pb-Ag (+ barite) deposits from the western Brooks Range. The deposits are hosted in black shale and carbonate rocks of the Late Mississippian-Early Pennsylvanian Kuna Formation. Quartz-pyrite-white mica grains in sedimentary rocks above the Anarraaq deposit yield an age of 195.0 ?? 2.0 Ma, and paragenetically late quartz-pyrite-white mica from the Main orebody at the Red Dog deposit has an age of 126.1 ?? 0.7 Ma. These white micas are much younger than the age of Zn-Pb-Ag mineralization at Red Dog (338 ?? 5.8 Ma Re-Os age of pyrite). The date for white mica from Anarraaq (???195 Ma) appears to be related to a large-scale thermal event in the region immediately before the inception of the Brooks Range orogeny. The white mica from the Red Dog deposit (???126 Ma) correlates with the later stages of the orogeny, a period of blueschist metamorphism, extension, and rapid exhumation, which varied with geographic location. These dates suggest that the Red Dog deposits underwent significant hydrothermal overprinting during multiple episodes of the Brooks Range orogeny. ?? 2004 by Economic Geology.

  14. Paleozoic sedimentary rocks in the Red Dog Zn-Pb-Ag district and vicinity, western Brooks Range, Alaska: provenance, deposition, and metallogenic significance

    USGS Publications Warehouse

    Slack, John F.; Dumoulin, Julie A.; Schmidt, J.M.; Young, L.E.; Rombach, Cameron

    2004-01-01

    The distribution and composition of Paleozoic strata in the western Brooks Range may have played a fundamental role in Zn-Pb mineralization of the Red Dog district. In our model, deposition and early lithification of biogenic chert and bedded siliceous rocks in the upper part of the Kuna Formation served as a regional hydrologic seal, acting as a cap rock to heat and hydrothermal fluids during Late Mississippian base-metal mineralization. Equally important was the iron-poor composition of black shales of the Kuna Formation (i.e., low Fe/Ti ratios), which limited synsedimentary pyrite formation in precursor sediments, resulting in significant H2S production in pore waters through the interaction of aqueous sulfate with abundant organic matter. This H2S may have been critical to the subsurface deposition of the huge quantities of Zn and Pb in the district. On the basis of this model, we propose that low Fe/Ti and S/C ratios in black shale sequences are potential basin-scale exploration guides for giant sediment-hosted, stratiform Zn-Pb-Ag deposits.

  15. Environmental geochemistry of shale-hosted Ag-Pb-Zn massive sulfide deposits in northwest Alaska: Natural background concentrations of metals in water from mineralized areas

    USGS Publications Warehouse

    Kelley, K.D.; Taylor, C.D.

    1997-01-01

    Red Dog, Lik and Drenchwater are shale-hosted stratiform Ag-Pb-Zn massive sulfide deposits in the northwestern Brooks Range. Natural background concentrations of metals in waters from the undisturbed (unmined) Drenchwater prospect and Lik deposit were compared to pre-mining baseline studies conducted at Red Dog. The primary factors affecting water chemistry are the extent of exposure of the deposits, the grade of mineralization, the presence of carbonate reeks in the section, and the proportion of Fe-sulfide in the ore. Surface water samples from the Drenchwater prospect, which has pyrite-dominant mineralization exposed in outcrop, have pH values as low as 2.8 and high dissolved concentrations of metals including as much as 95 mg 1-1 Al, 270 mg 1-1 Fe, 8 ??1-1 Cd, 10 ??1-1 Pb, and 2600 ??1-1 Zn, with As up to 26 ??g1-1. Surface waters from the Red Dog deposit prior to mining were also acidic and metal-rich, however, dissolved metal concentrations in Red Dog waters were many times greater. The higher metal concentrations in Red Dog waters reflect the high Zn grades and the abundant sphalerite, pyrite, and galena that were present in outcrop prior to mining. In contrast, despite significant mineralization at the Lik deposit, carbonate rocks in the section buffer the system, resulting in less acidic, mostly near-neutral pH values with low concentrations of most metals except Zn.

  16. Metal dispersion and mobility in soils from the Lik Zn-Pb-Ag massive sulphide deposit, NW Alaska: Environmental and exploration implications

    USGS Publications Warehouse

    Kelley, K.D.; Kelley, D.L.

    2003-01-01

    The Lik deposit in northern Alaska is a largely unexposed shale-hosted Zn-Pb-Ag massive sulphide deposit that is underlain by continuous permafrost. Residual soils overlying the mineralized zone have element enrichments that are two to six times greater than baseline values. The most prominent elements are Ag, Mo, P, Se, Sr, V by total 4-acid digestion and Tl by a weak partial digestion (Enzyme Leach or EL) because they show multi-point anomalies that extend across the entire mineralized zone, concentration ranges are 0.5-2.6 ppm Ag, 4-26 ppm Mo, 0.1-0.3% P, 3-22 ppm Se, 90-230 ppm Sr, 170-406 ppm V, and 1.6-30 ppb Tl. Lead, Sb, and Hg are also anomalous (up to 178 ppm, 30 ppm, and 1.9 ppm, respectively), but all are characterized by single point anomalies directly over the mineralized zone, with only slightly elevated concentrations over the lower mineralized section. Zinc (total) has a consistent baseline response of 200 ppm, but it is not elevated in soils overlying the mineralized zone. However, Zn by EL shows a distinct single-point anomaly over the ore zone that suggests it was highly mobile and partly adsorbed on oxides or other secondary phases during weathering. In situ analyses (by laser ablation ICP-MS) of pyrite and sphalerite from drill core suggest that sphalerite is the primary residence for Ag, Cd, and Hg in addition to Zn, and pyrite contains As, Fe, Sb, and Tl. The level and degree of oxidation, and the proportion of reacting pyrite and carbonate minerals are two factors that affected the mobility and transport of metals. In oxidizing conditions, Zn is highly mobile relative to Hg and Ag, perhaps explaining the decoupling of Zn from the other sphalerite-hosted elements in the soils. Soils are acidic (to 3.9 pH) directly over the deposit due to the presence of acid-producing pyrite, but acid-neutralizing carbonate away from the mineralized zone yield soils that are near neutral. The soils therefore formed in a complex system involving oxidation and

  17. 40Ar/39Ar Dating of Zn-Pb-Ag Mineralization in the Northern Brooks Range, Alaska

    USGS Publications Warehouse

    Werdon, Melanie B.; Layer, Paul W.; Newberry, Rainer J.

    2004-01-01

    The 40Ar/39Ar laser step-heating method potentially can be used to provide absolute ages for a number of formerly undatable, low-temperature ore deposits. This study demonstrates the use of this method by determining absolute ages for Zn-Pb-Ag sediment-hosted massive sulfide deposits and vein-breccia occurrences found throughout a 300-km-long, east-west-trending belt in the northern Brooks Range, Alaska. Massive sulfide deposits are hosted by Mississippian to Pennsylvanian(?) black carbonaceous shale, siliceous mudstone, and lesser chert and carbonate turbidites of the Kuna Formation (e.g., Red Dog, Anarraaq, Lik (Su), and Drenchwater). The vein-breccia occurrences (e.g., Husky, Story Creek, West Kivliktort Mountain, Vidlee, and Kady) are hosted by a deformed but only weakly metamorphosed package of Upper Devonian to Lower Mississippian mixed continental and marine clastic rocks (the Endicott Group) that stratigraphically underlie the Kuna Formation. The vein-breccias are mineralogically similar to, but not spatially associated with, known massive sulfide deposits. The region's largest shale-hosted massive sulfide deposit is Red Dog; it has reserves of 148 Mt grading 16.6 percent zinc, 4.5 percent lead, and 77 g of silver per tonne. Hydrothermally produced white mica in a whole-rock sample from a sulfide-bearing igneous sill within the Red Dog deposit yielded a plateau age of 314.5 Ma. The plateau age of this whole-rock sample records the time at which temperatures cooled below the argon closure temperature of the white mica and is interpreted to represent the minimum age limit for massive sulfide-related hydrothermal activity in the Red Dog deposit. Sulfide-bearing quartz veins at Drenchwater crosscut a hypabyssal intrusion with a maximum biotite age of 337.0 Ma. Despite relatively low sulfide deposition temperatures in the vein-breccia occurrences (162°-251°C), detrital white mica in sandstone immediately adjacent to large vein-breccia zones was partially to

  18. Geological, fluid inclusion and isotopic studies of the Baiyangping Pb-Zn-Cu-Ag polymetallic deposit, Lanping basin, Yunnan province, China

    NASA Astrophysics Data System (ADS)

    Wang, Xiao-Hu; Hou, Zeng-Qian; Song, Yu-Cai; Zhang, Hong-Rui

    2015-11-01

    Baiyangping Pb-Zn-Cu-Ag deposit is located in Lanping basin, northwestern Yunnan province. The deposit is composed of a few ore veins and can be divided into several ore blocks. The ore bodies are primarily hosted in Mesozoic carbonate, sandstone and siltstone along the north-south-striking, NWW-striking and NE-SW-striking fault zones. There are breccia, massive, vein like and disseminated ores. The main ore minerals are sphalerite, galena, gratonite, jordanite, tetrahedrite series minerals, chalcocite, chalcopyrite, realgar, orpiment, bournonite, cobalt-bearing arsenopyrite, argentite, kongsbergite, cobaltine, siegenite. The sizes of fluid inclusions in Baiyangping deposit are generally less than 10 μm and have the shape of round, oval, irregular, etc. The ore-forming fluid system is Ca2+-Na+-K+-Mg2+-Cl--F--NO3- brine system. The freezing temperature of fluid inclusions in mineral deposits ranges from -26.4 to -0.2 °C, average -14.6 °C; the homogenization temperature is concentrated in 120-180 °C, and the salinity is between 0.35 and 24.73 wt% (NaCleq), average 16.9 wt% (NaCleq). δ13CPDB and δ18OSMOW values of hydrothermal calcite range from -4.16‰ to 3‰ and -2.5‰ to 20.4‰, respectively. δ34S values of sulfide minerals range from -10.2‰ to 11.2‰, average 5.6‰. The sulfide samples yield 206Pb/204Pb values of 18.609-18.818, 207Pb/204Pb of 15.548-15.842 and 208Pb/204Pb = 38.514-39.556. C-O-S-Pb isotope compositions of the Baiyangping deposit indicate a homogeneous carbon source, and the carbon in hydrothermal calcite is derived from the dissolution of carbonate rock strata, the ore-forming fluid belongs to basin brine fluid system, which is mixed with the precipitate water, sulfur in sulfides and sulfosalts is derived from thermal chemical sulfate reduction, and the thermal decomposition of sulfur-bearing organic matter. The metal mineralization material is from sedimentary strata and basement. The late Pb-Zn polymetallic mineralization event

  19. Flowing Liquid Anode Atmospheric Pressure Glow Discharge as an Excitation Source for Optical Emission Spectrometry with the Improved Detectability of Ag, Cd, Hg, Pb, Tl, and Zn.

    PubMed

    Greda, Krzysztof; Swiderski, Krzysztof; Jamroz, Piotr; Pohl, Pawel

    2016-09-01

    A novel atmospheric pressure glow discharge generated in contact with a flowing liquid anode (FLA-APGD) was developed as the efficient excitation source for the optical emission spectrometry (OES) detection. Differences in the appearance and the electrical characteristic of the FLA-APGD and a conventional system operated with a flowing liquid cathode (FLC-APGD) were studied in detail and discussed. Under the optimal operating conditions for the FLA-APGD, the emission from the analytes (Ag, Cd, Hg, Pb, Tl, and Zn) was from 20 to 120 times higher as compared to the FLC-APGD. Limits of detections (LODs) established with a novel FLA-APGD system were on average 20 times better than those obtained for the FLC-APGD. A further improvement of the LODs was achieved by reducing the background shift interferences and, as a result, the LODs for Ag, Cd, Hg, Pb, Tl, and Zn were 0.004, 0.040, 0.70, 1.7, 0.035, and 0.45 μg L(-1), respectively. The precision of the FLA-APGD-OES method was evaluated to be within 2-5% (as the relative standard deviation of the repeated measurements). The method found its application in the determination of the content of Ag, Cd, Hg, Pb, Tl, and Zn in a certified reference material (CRM) of Lobster hepatopancreas (TORT-2), four brass samples as well as mineral water and tea leaves samples spiked with the analytes. In the case of brass samples, a reference method, i.e., inductively coupled plasma optical emission spectrometry (ICP-OES) was used. A good agreement between the results obtained with FLA-APGD-OES and the certified values for the CRM TORT-2 as well as the reference values obtained with ICP-OES for the brass samples was revealed, indicating the good accuracy of the proposed method. The recoveries obtained for the spiked samples of mineral water and tea leaves were within the range of 97.5-102%. PMID:27476678

  20. Carbonate-replacement Pb-Zn-Ag ± Au mineralization in the Kamariza area, Lavrion, Greece: Mineralogy and thermochemical conditions of formation

    NASA Astrophysics Data System (ADS)

    Voudouris, P.; Melfos, V.; Spry, P. G.; Bonsall, T. A.; Tarkian, M.; Solomos, Ch.

    2008-09-01

    Carbonate-replacement Pb-Zn-Ag ± Au deposits in the Kamariza area, Lavrion district, Attica, Greece, are genetically related to the emplacement of Miocene andesitic dikes within a rapidly extending continental back-arc basin, which formed during exhumation of the Attic-Cycladic Crystalline Belt. Replacement veins as well as chimneys and mantos of massive sulfides are the major orebody types with mantos grading into chimneys and veins. Ore minerals are similar among the various types of orebodies in the Kamariza area and consist of sulfides and sulfarsenides (pyrite, arsenopyrite, chalcopyrite, galena, sphalerite, gersdorffite, marcasite), native metals (Au and Bi), Sn-bearing phases (petrukite), sulfosalts and sulfbismuthites of Ag, Bi, Cu, Pb, As, Sb (tetrahedrite-group minerals, bournonite, boulangerite, stephanite, pyrargyrite, semseyite, enargite, bismuthinite, lillianite homologues, Cu-matildite, aikinite, Ag-aikinite, mummeite, emplectite, wittichenite). The elemental association of Bi, Au, and Ag is common. The assemblages gersdorffite-bismuthinite-native gold and native gold-native bismuth are evidence for a contribution of magmatic components to the hydrothermal system. A fluctuation in the sulfidation states of the ore fluid during the evolution of the Kamariza system is evident from the deposition of early arsenopyrite, as well as of enargite-luzonite and both low-Fe and Fe-rich sphalerite in the same samples. Microthermometry of fluid inclusion assemblages show that carbonate replacement mineralization was deposited from a warm to hot (100°C to 400°C), low to moderately saline (1.8 to 17.3 wt% NaCl equiv) fluid. Eutectic temperatures of fluid inclusions as low as -55°C suggest the presence of CaCl2 in addition to NaCl, in the ore fluid. The Kamariza deposit occurs distal to the Plaka granodiorite intrusion and the associated porphyry-Mo mineralization, but is likely to be genetically related to a granitoid buried at depth.

  1. Coupled heat and fluid flow modeling of the Carboniferous Kuna Basin, Alaska: Implications for the genesis of the Red Dog Pb-Zn-Ag-Ba ore district

    USGS Publications Warehouse

    Garven, G.; Raffensperger, J.P.; Dumoulin, J.A.; Bradley, D.A.; Young, L.E.; Kelley, K.D.; Leach, D.L.

    2003-01-01

    The Red Dog deposit is a giant 175 Mton (16% Zn, 5% Pb), shale-hosted Pb-Zn-Ag-Ba ore district situated in the Carboniferous Kuna Basin, Western Brooks Range, Alaska. These SEDEX-type ores are thought to have formed in calcareous turbidites and black mudstone at elevated sub-seafloor temperatures (120-150??C) within a hydrogeologic framework of submarine convection that was structurally organized by large normal faults. The theory for modeling brine migration and heat transport in the Kuna Basin is discussed with application to evaluating flow patterns and heat transport in faulted rift basins and the effects of buoyancy-driven free convection on reactive flow and ore genesis. Finite element simulations show that hydrothermal fluid was discharged into the Red Dog subbasin during a period of basin-wide crustal heat flow of 150-160 mW/m2. Basinal brines circulated to depths as great as 1-3 km along multiple normal faults flowed laterally through thick clastic aquifers acquiring metals and heat, and then rapidly ascended a single discharge fault zone at rates ??? 5 m/year to mix with seafloor sulfur and precipitate massive sulfide ores. ?? 2003 Elsevier Science B.V. All rights reserved.

  2. Ideal Weyl Semimetals in the Chalcopyrites CuTlSe2 , AgTlTe2 , AuTlTe2 , and ZnPbAs2

    NASA Astrophysics Data System (ADS)

    Ruan, Jiawei; Jian, Shao-Kai; Zhang, Dongqin; Yao, Hong; Zhang, Haijun; Zhang, Shou-Cheng; Xing, Dingyu

    2016-06-01

    Weyl semimetals are new states of matter which feature novel Fermi arcs and exotic transport phenomena. Based on first-principles calculations, we report that the chalcopyrites CuTlSe2 , AgTlTe2 , AuTlTe2 , and ZnPbAs2 are ideal Weyl semimetals, having largely separated Weyl points (˜0.05 Å-1 ) and uncovered Fermi arcs that are amenable to experimental detections. We also construct a minimal effective model to capture the low-energy physics of this class of Weyl semimetals. Our discovery is a major step toward a perfect playground of intriguing Weyl semimetals and potential applications for low-power and high-speed electronics.

  3. Ideal Weyl Semimetals in the Chalcopyrites CuTlSe_{2}, AgTlTe_{2}, AuTlTe_{2}, and ZnPbAs_{2}.

    PubMed

    Ruan, Jiawei; Jian, Shao-Kai; Zhang, Dongqin; Yao, Hong; Zhang, Haijun; Zhang, Shou-Cheng; Xing, Dingyu

    2016-06-01

    Weyl semimetals are new states of matter which feature novel Fermi arcs and exotic transport phenomena. Based on first-principles calculations, we report that the chalcopyrites CuTlSe_{2}, AgTlTe_{2}, AuTlTe_{2}, and ZnPbAs_{2} are ideal Weyl semimetals, having largely separated Weyl points (∼0.05  Å^{-1}) and uncovered Fermi arcs that are amenable to experimental detections. We also construct a minimal effective model to capture the low-energy physics of this class of Weyl semimetals. Our discovery is a major step toward a perfect playground of intriguing Weyl semimetals and potential applications for low-power and high-speed electronics. PMID:27314733

  4. The Drenchwater deposit, Alaska: An example of a natural low pH environment resulting from weathering of an undisturbed shale-hosted Zn-Pb-Ag deposit

    USGS Publications Warehouse

    Graham, G.E.; Kelley, K.D.

    2009-01-01

    The Drenchwater shale-hosted Zn-Pb-Ag deposit and the immediate vicinity, on the northern flank of the Brooks Range in north-central Alaska, is an ideal example of a naturally low pH system. The two drainages, Drenchwater and False Wager Creeks, which bound the deposit, differ in their acidity and metal contents. Moderately acidic waters with elevated concentrations of metals (pH ??? 4.3, Zn ??? 1400 ??g/L) in the Drenchwater Creek drainage basin are attributed to weathering of an exposed base-metal-rich massive sulfide occurrence. Stream sediment and water chemistry data collected from False Wager Creek suggest that an unexposed base-metal sulfide occurrence may account for the lower pH (2.7-3.1) and very metal-rich waters (up to 2600 ??g/L Zn, ??? 260 ??g/L Cu and ???89 ??g/L Tl) collected at least 2 km upstream of known mineralized exposures. These more acidic conditions produce jarosite, schwertmannite and Fe-hydroxides commonly associated with acid-mine drainage. The high metal concentrations in some water samples from both streams naturally exceed Alaska state regulatory limits for freshwater aquatic life, affirming the importance of establishing base-line conditions in the event of human land development. The studies at the Drenchwater deposit demonstrate that poor water quality can be generated through entirely natural weathering of base-metal occurrences, and, possibly unmineralized black shale.

  5. The Luanchuan Mo-W-Pb-Zn-Ag magmatic-hydrothermal system in the East Qinling metallogenic belt, China: Constrains on metallogenesis from C-H-O-S-Pb isotope compositions and Rb-Sr isochron ages

    NASA Astrophysics Data System (ADS)

    Cao, Hua-Wen; Zhang, Shou-Ting; Santosh, M.; Zheng, Luo; Tang, Li; Li, Dong; Zhang, Xu-Huang; Zhang, Yun-Hui

    2015-11-01

    The Luanchuan Mo-W-Pb-Zn-Ag polymetallic ore district is located in the East Qinling metallogenic belt on the southern margin of the North China Craton. Two ore fields (Nannihu and Yuku) are recognized in the district, and three types of deposits are identified from the two ore fields as follows: (1) the 6 proximal porphyry-skarn type Mo-W deposits occurring at the inner contact zone of the granite porphyries, (2) the 3 middle skarn-hydrothermal type Zn deposits, and (3) the 8 distal hydrothermal type Pb-Zn-Ag deposits at the periphery of the porphyry. We present C-H-O isotope compositions of hydrothermal quartz and calcite, S-Pb isotope compositions of sulfide minerals, and sphalerite Rb-Sr isochron ages from the 17 deposits. The geochemical and geochronological data from the two ore fields all show systematic temporal and spatial variation, and primarily lead to the following inferences. (1) The temperatures and salinities of the ore-forming fluids decreased during mineralization. The ore-forming fluids gradually evolved from magmatic water to mixed magmatic-meteoric water. (2) The metallogenic components were primarily derived from igneous rocks, with increasing proportions of the materials from the ore-bearing rocks. (3) The mineralization ages of these deposits are close (147-136 Ma), which correspond to the emplacement of the granite intrusions. (4) The three types of deposits and the ore-related late Mesozoic intrusives constitute a unified magmatic-hydrothermal-mineralization system. Finally, we also suggest exploration strategies for the Luanchuan ore district.

  6. Clastic-hosted stratiform, vein/breccia and disseminated Zn-Pb-Ag deposits of the northwestern Brooks Range, AK: Are they different expressions of dewatering of the same source basin

    SciTech Connect

    Schmidt, J.M. ); Werdon, M.B. . Dept. of Geology)

    1993-04-01

    Sphalerite and galena, with significant silver occur in 3 distinct types of mineralization hosted in Upper Devonian and Carboniferous clastic rocks of the northwestern Brooks Range. The best known are Zn-Pb-Ag massive sulfide deposits with variable pyrite, barite, and hydrothermal silifica hosted in Mississippian (to Pennsylvanian ) black siliceous shale and chert, and similar to shale-hosted Pb-Zn massive sulfide deposits worldwide. Zn-Pb-Ag breccias and veins are hosted in Upper Devonian to Lower Mississippian fine-grained quartzites and siltstone which stratigraphically underlie the massive sulfide-hosting units. The breccia-vein and disseminated occurrences are co-extensive with the rocks that host massive sulfide deposits, and with the western part of the Endicott Group clastic basin. Pb isotopic ratios of galena from all the deposits are remarkably uniform, and suggest a single Pb source. The authors genetic model suggests that all types are the result of dewatering of a single clastic source basin. Different mineralization styles are probably due to variable depths of emplacement (at or below the seafloor), thermal variations related to extensional thinning of the crust, and hydrologic flow out of the basin controlled by extensional thinning of the crust, and hydrologic flow out of the basin controlled by extensional faulting and permeability variations in local stratigraphy. The most likely sources for Zn and Pb are clay minerals within the lowermost (Hunt Fork Shale) portions of the western Endicott Group.

  7. Positive feedback between strain localization and fluid flow at the ductile-brittle transition leading to Pb-Zn-Fe-Cu-Ag ore deposits in Lavrion (Greece)

    NASA Astrophysics Data System (ADS)

    Scheffer, Christophe; Tarantola, Alexandre; Vanderhaeghe, Olivier

    2016-04-01

    At the crustal scale, the ductile-brittle transition (DBT) might correspond to a physical barrier that separates a deep reservoir of metamorphic and magmatic fluids from a shallow reservoir of surficial fluids. Rock rheology, and thus the location of the DBT, is mainly governed by lithology, temperature and the presence/absence of fluids. Accordingly, the position of the DBT potentially evolves during orogenic evolution owing to thermal evolution and fluid circulation. In turn rocks are transferred across it during burial and exhumation. These processes induce connections between fluid reservoirs which might play a role on ore deposition. In this contribution, we discuss the impact of lithological heterogeneities on deformation, fluid flow and ore deposition based on the example of the Lavrion low-angle top-to-the-SSW detachment accommodating gravitational collapse of the Hellenides orogenic belt in Greece. The Lavrion peninsula, localized along the western boundary of the Attic-Cycladic Metamorphic Core Complex, is characterized by Pb-Zn-Fe-Cu-Ag ore mineralization mainly concentrated along a lithological contact (marble/schists) below and within a detachment shear zone. The mylonitic marble below the detachment shear zone is composed of white layers of pure marble alternating with blue layers containing impurities (SiO2, Al2O3, organic matter…). Development of the mylonitic fabric in competent impure blue marble is associated with its preferred dolomitization related to focused fluid infiltration. This mylonitic marble is cross-cut by several cataclastic horizons preferentially developed within the more competent impure blue marble and newly-crystallized dolomitic horizon. These cataclasites are invaded by fluorite and calcite gangue minerals showing locally Mn, Pb, Zn, Fe oxides and/or hydroxides, sphalerite, Ag-galena, Ag-sulfur and native Ag. Oxygen and carbon stable isotopes performed on marble sections point out decarbonation with magmatic contribution and

  8. Geological and isotopic evidence for magmatic-hydrothermal origin of the Ag-Pb-Zn deposits in the Lengshuikeng District, east-central China

    NASA Astrophysics Data System (ADS)

    Wang, Changming; Zhang, Da; Wu, Ganguo; Santosh, M.; Zhang, Jing; Xu, Yigan; Zhang, Yaoyao

    2014-08-01

    The Lengshuikeng ore district in east-central China has an ore reserve of ˜43 Mt with an average grade of 204.53 g/t Ag and 4.63 % Pb + Zn. Based on contrasting geological characteristics, the mineralization in the Lengshuikeng ore district can be divided into porphyry-hosted and stratabound types. The porphyry-hosted mineralization is distributed in and around the Lengshuikeng granite porphyry and shows a distinct alteration zoning including minor chloritization and sericitization in the proximal zone; sericitization, silicification, and carbonatization in the peripheral zone; and sericitization and carbonatization in the distal zone. The stratabound mineralization occurs in volcano-sedimentary rocks at ˜100-400 m depth without obvious zoning of alterations and ore minerals. Porphyry-hosted and stratabound mineralization are both characterized by early-stage pyrite-chalcopyrite-sphalerite, middle-stage acanthite-native silver-galena-sphalerite, and late-stage pyrite-quartz-calcite. The δ34S values of pyrite, sphalerite, and galena in the ores range from -3.8 to +6.9‰ with an average of +2.0‰. The C-O isotope values of siderite, calcite, and dolomite range from -7.2 to -1.5‰ with an average of -4.4‰ (V-PDB) and from +10.9 to +19.5‰ with an average of +14.8‰ (V-SMOW), respectively. Hydrogen, oxygen, and carbon isotopes indicate that the hydrothermal fluids were derived mainly from meteoric water, with addition of minor amounts of magmatic water. Geochronology employing LA-ICP-MS analyses of zircons from a quartz syenite porphyry yielded a weighted mean 206Pb/238U age of 136.3 ± 0.8 Ma considered as the emplacement age of the porphyry. Rb-Sr dating of sphalerite from the main ore stage yielded an age of 126.9 ± 7.1 Ma, marking the time of mineralization. The Lengshuikeng mineralization classifies as an epithermal Ag-Pb-Zn deposit.

  9. Formation of the Wiesloch Mississippi Valley-type Zn-Pb-Ag deposit in the extensional setting of the Upper Rhinegraben, SW Germany

    USGS Publications Warehouse

    Pfaff, Katharina; Hildebrandt, Ludwig H.; Leach, David L.; Jacob, Dorrit E.; Markl, Gregor

    2010-01-01

    The Mississippi Valley-type (MVT) Zn-Pb-Ag deposit in the Wiesloch area, Southwest Germany, is controlled by graben-related faults of the Upper Rhinegraben. Mineralization occurs as vein fillings and irregular replacement ore bodies consisting of sphalerite, banded sphalerite, galena, pyrite, sulfosalts (jordanite and geocronite), barite, and calcite in the Middle Triassic carbonate host rock. Combining paragenetic information, fluid inclusion investigations, stable isotope and mineral chemistry with thermodynamic modeling, we have derived a model for the formation of the Wiesloch deposit. This model involves fluid mixing between ascending hot brines (originating in the crystalline basement) with sedimentary formation waters. The ascending brines originally had a near-neutral pH (around 6) and intermediate oxidation state, reflecting equilibrium with granites and gneisses in the basement. During fluid ascent and cooling, the pH of the brine shifted towards more acidic (around 4) and the oxidation state increased to conditions above the hematite-magnetite buffer. These chemical characteristics contrast strongly with those of the pore and fracture fluid residing in the limestone aquifer, which had a pH between 8 and 9 in equilibrium with calcite and was rather reduced due to the presence of organic matter in the limestone. Mixing between these two fluids resulted in a strong decrease in the solubility of silver-bearing sphalerite and galena, and calcite. Besides Wiesloch, several Pb-Zn deposits are known along the Upper Rhinegraben, including hydrothermal vein-type deposits like Badenweiler and the Michael mine near Lahr. They all share the same fluid origin and formation process and only differ in details of their host rock and fluid cooling paths. The mechanism of fluid mixing also seems to be responsible for the formation of other MVT deposits in Europe (e.g., Reocin, Northern Spain; Treves, Southern France; and Cracow-Silesia, Poland), which show notable

  10. Depositional conditions for the Kuna Formation, Red Dog Zn-PB-Ag-Barite District, Alaska, inferred from isotopic and chemical proxies

    USGS Publications Warehouse

    Johnson, Craig A.; Dumoulin, Julie A.; Burruss, Robert A.; Slack, John F.

    2015-01-01

    Water column redox conditions, degree of restriction of the depositional basin, and other paleoenvironmental parameters have been determined for the Mississippian Kuna Formation of northwestern Alaska from stratigraphic profiles of Mo, Fe/Al, and S isotopes in pyrite, C isotopes in organic matter, and N isotopes in bulk rock. This unit is important because it hosts the Red Dog and Anarraaq Zn-Pb-Ag ± barite deposits, which together constitute one of the largest zinc resources in the world. The isotopic and chemical proxies record a deep basin environment that became isolated from the open ocean, became increasingly reducing, and ultimately became euxinic. The basin was ventilated briefly and then became isolated again just prior to its demise as a discrete depocenter with the transition to the overlying Siksikpuk Formation. Ventilation corresponded approximately to the initiation of bedded barite deposition in the district, whereas the demise of the basin corresponded approximately to the formation of the massive sulfide deposits. The changes in basin circulation during deposition of the upper Kuna Formation may have had multiple immediate causes, but the underlying driver was probably extensional tectonic activity that also facilitated fluid flow beneath the basin floor. Although the formation of sediment-hosted sulfide deposits is generally favored by highly reducing conditions, the Zn-Pb deposits of the Red Dog district are not found in the major euxinic facies of the Kuna basin, nor did they form during the main period of euxinia. Rather, the deposits occur where strata were permeable to migrating fluids and where excess H2S was available beyond what was produced in situ by decomposition of local sedimentary organic matter. The known deposits formed mainly by replacement of calcareous strata that gained H2S from nearby highly carbonaceous beds (Anarraaq deposit) or by fracturing and vein formation in strata that produced excess H2S by reductive dissolution of

  11. Trace elements in Zn Pb Ag deposits and related stream sediments, Brooks Range Alaska, with implications for Tl as a pathfinder element

    USGS Publications Warehouse

    Graham, G.E.; Kelley, K.D.; Slack, J.F.; Koenig, A.E.

    2009-01-01

    The Zn-Pb-Ag metallogenic province of the western and central Brooks Range, Alaska, contains two distinct but mineralogically similar deposit types: shale-hosted massive sulphide (SHMS) and smaller vein-breccia occurrences. Recent investigations of the Red Dog and Anarraaq SHMS deposits demonstrated that these deposits are characterized by high trace-element concentrations of As, Ge, Sb and Tl. This paper examines geochemistry of additional SHMS deposits (Drenchwater and Su-Lik) to determine which trace elements are ubiquitously elevated in all SHMS deposits. Data from several vein-breccia occurrences are also presented to see if trace-element concentrations can distinguish SHMS deposits from vein-breccia occurrences. Whole-rock geochemical data indicate that Tl is the most consistently and highly concentrated characteristic trace element in SHMS deposits relative to regional unmineralized rock samples. Laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) analyses of pyrite and sphalerite indicate that Tl is concentrated in pyrite in SHMS. Stream sediment data from the Drenchwater and Su-Lik SHMS show that high Tl concentrations are more broadly distributed proximal to known or suspected mineralization than As, Sb, Zn and Pb anomalies. This broader distribution of Tl in whole-rock and particularly stream sediment samples increases the footprint of exposed and shallowly buried SHMS mineralization. High Tl concentrations also distinguish SHMS mineralization from the vein-breccia deposits, as the latter lack high concentrations of Tl but can otherwise have similar trace-element signatures to SHMS deposits. ?? 2009 AAG/Geological Society of London.

  12. Timing of porphyry (Cu-Mo) and base metal (Zn-Pb-Ag-Cu) mineralisation in a magmatic-hydrothermal system—Morococha district, Peru

    NASA Astrophysics Data System (ADS)

    Catchpole, Honza; Kouzmanov, Kalin; Bendezú, Aldo; Ovtcharova, Maria; Spikings, Richard; Stein, Holly; Fontboté, Lluís

    2015-12-01

    The Morococha district in central Peru is characterised by economically important Cordilleran polymetallic (Zn-Pb-Ag-Cu) vein and replacement bodies and the large Toromocho porphyry Cu-Mo deposit in its centre. U-Pb, Re-Os, and 40Ar/39Ar geochronology data for various porphyry-related hydrothermal mineralisation styles record a 3.5-Ma multi-stage history of magmatic-hydrothermal activity in the district. In the late Miocene, three individual magmatic-hydrothermal centres were active: the Codiciada, Toromocho, and Ticlio centres, each separated in time and space. The Codiciada centre is the oldest magmatic-hydrothermal system in the district and consists of a composite porphyry stock associated with anhydrous skarn and quartz-molybdenite veins. The hydrothermal events are recorded by a titanite U-Pb age at 9.3 ± 0.2 Ma and a molybdenite Re-Os age at 9.26 ± 0.03 Ma. These ages are indistinguishable from zircon U-Pb ages for porphyry intrusions of the composite stock and indicate a time span of 0.2 Ma for magmatic-hydrothermal activity. The small Ticlio magmatic-hydrothermal centre in the west of the district has a maximum duration of 0.3 Ma, ranging from porphyry emplacement to porphyry mineralisation at 8.04 ± 0.14 Ma (40Ar/39Ar muscovite cooling age). The Toromocho magmatic-hydrothermal centre has a minimum of five recorded porphyry intrusions that span a total of 1.3 Ma and is responsible for the formation of the giant Toromocho Cu-Mo deposit. At least two hydrothermal pulses are identified. Post-dating a first pulse of molybdenite mineralisation, wide-spread hydrous skarn covers an area of over 6 km2 and is recorded by five 40Ar/39Ar cooling ages at 7.2-6.8 Ma. These ages mark the end of the slowly cooling and long-lived Toromocho magmatic-hydrothermal centre soon after last magmatic activity at 7.26 ± 0.02 Ma. District-wide (50 km2) Cordilleran base metal vein and replacement bodies post-date the youngest recorded porphyry mineralisation event at Toromocho

  13. The chemistry and origin of zincian spinel associated with the Aggeneys Cu-Pb-Zn-Ag deposits, Namaqualand, South Africa

    NASA Astrophysics Data System (ADS)

    Spry, P. G.

    1987-10-01

    Zincian spinel or gahnite [(Zn,Fe,Mg)Al2O4] occurs in metamorphosed sulphide-rich rocks, garnet quartzites, quartz-magnetite rocks, aluminous metasediments, barite-magnetite rocks, quartz veins, and pegmatites associated with the Aggeneys base metal deposits, Namaqualand, South Africa. Zincian spinel in, sulphide-bearing rocks, is considered to have formed predominantly by desulphurization reactions involving a member of the system Fe-S-O and sphalerite with sillimanite or garnet. Gahnite in sulphide-free garnet quartzites, quartz-magnetite rocks and barite-magnetite rocks probably formed from Zn and Al that were hydrothermally derived whereas gahnite in aluminous metasediments was derived from the metamorphism of metalliferous shales, in which Zn may originally have been linked to organic material. Gahnite is Zn-rich in sulphide-bearing rock, but is Fe-rich in sulphide-free garnet quartzites and quartz-magnetite rocks. Although Zn-rich spinels represent guides to ore in the Aggeneys area and elsewhere in the Namaqualand Metamorphic Complex, Fe-rich spinels should not be discounted because Zn-rich and Fe-rich spinels occur within metres of sulphides at Aggeneys.

  14. Formation of the Wiesloch Mississippi Valley-type Zn-Pb-Ag deposit in the extensional setting of the Upper Rhinegraben, SW Germany

    NASA Astrophysics Data System (ADS)

    Pfaff, Katharina; Hildebrandt, Ludwig H.; Leach, David L.; Jacob, Dorrit E.; Markl, Gregor

    2010-10-01

    The Mississippi Valley-type (MVT) Zn-Pb-Ag deposit in the Wiesloch area, Southwest Germany, is controlled by graben-related faults of the Upper Rhinegraben. Mineralization occurs as vein fillings and irregular replacement ore bodies consisting of sphalerite, banded sphalerite, galena, pyrite, sulfosalts (jordanite and geocronite), barite, and calcite in the Middle Triassic carbonate host rock. Combining paragenetic information, fluid inclusion investigations, stable isotope and mineral chemistry with thermodynamic modeling, we have derived a model for the formation of the Wiesloch deposit. This model involves fluid mixing between ascending hot brines (originating in the crystalline basement) with sedimentary formation waters. The ascending brines originally had a near-neutral pH (around 6) and intermediate oxidation state, reflecting equilibrium with granites and gneisses in the basement. During fluid ascent and cooling, the pH of the brine shifted towards more acidic (around 4) and the oxidation state increased to conditions above the hematite-magnetite buffer. These chemical characteristics contrast strongly with those of the pore and fracture fluid residing in the limestone aquifer, which had a pH between 8 and 9 in equilibrium with calcite and was rather reduced due to the presence of organic matter in the limestone. Mixing between these two fluids resulted in a strong decrease in the solubility of silver-bearing sphalerite and galena, and calcite. Besides Wiesloch, several Pb-Zn deposits are known along the Upper Rhinegraben, including hydrothermal vein-type deposits like Badenweiler and the Michael mine near Lahr. They all share the same fluid origin and formation process and only differ in details of their host rock and fluid cooling paths. The mechanism of fluid mixing also seems to be responsible for the formation of other MVT deposits in Europe (e.g., Réocin, Northern Spain; Trèves, Southern France; and Cracow-Silesia, Poland), which show notable

  15. Critical elements in sediment-hosted deposits (clastic-dominated Zn-Pb-Ag, Mississippi Valley-type Zn-Pb, sedimentary rock-hosted Stratiform Cu, and carbonate-hosted Polymetallic Deposits): A review: Chapter 12

    USGS Publications Warehouse

    Marsh, Erin; Hitzman, Murray W.; Leach, David L.

    2016-01-01

    Some sediment-hosted base metal deposits, specifically the clastic-dominated (CD) Zn-Pb deposits, carbonate-hosted Mississippi Valley-type (MVT) deposits, sedimentary-rock hosted stratiform copper deposits, and carbonate-hosted polymetallic (“Kipushi type”) deposits, are or have been important sources of critical elements including Co, Ga, Ge, and Re. The generally poor data concerning trace element concentrations in these types of sediment-hosted ores suggest that there may be economically important concentrations of critical elements yet to be recognized.

  16. Re-Os sulfide geochronology of the Red Dog sediment-hosted Zn-Pb-Ag deposit, Brooks Range, Alaska

    USGS Publications Warehouse

    Morelli, R.M.; Creaser, R.A.; Selby, D.; Kelley, K.D.; Leach, D.L.; King, A.R.

    2004-01-01

    The Red Dog sediment-hosted deposit in the De Long Mountains of northern Alaska is the largest Zn producer in the world. Main stage mineralization is characterized by massive sulfide ore and crosscutting subvertical veins. Although the vein mineralization is clearly younger than the massive ore, the exact temporal relationship between the two is unclear. Re-Os geochronology of pyrite is used to determine the absolute age of main stage ore at Red Dog. A 10-point isochron on both massive and vein pyrite yields an age of 338.3 ?? 5.8 Ma and is interpreted to represent the age of main stage ore. The Re-Os data indicate that both massive and vein ore types are coeval within the resolution of the technique. Formation of the Red Dog deposit was associated with extension along a passive continental margin, and therefore the Re-Os age of main stage ore constrains the timing of rifting as well as the age of the host sedimentary rocks. Sphalerite from both massive and vein ore yields imprecise ages and shows a high degree of scatter compared to pyrite. We suggest that the Re-Os systematics of sphalerite can be disturbed and that this mineral is not reliable for Re-Os geochronology. ?? 2004 by Economic Geology.

  17. Cierco Pb-Zn-Ag vein deposits: Isotopic and fluid inclusion evidence for formation during the mesozoic extension in the pyrenees of Spain

    USGS Publications Warehouse

    Johnson, C.A.; Cardellach, E.; Tritlla, J.; Hanan, B.B.

    1996-01-01

    The Cierco Pb-Zn-Ag vein deposits, located in the central Pyrenees of Spain, crosscut Paleozoic metasedimentary rocks and are in close proximity to Hercynian granodiorite dikes and plutons. Galena and sphalerite in the deposits have average ??34S values of -4.3 and -0.8 per mil (CDT), respectively. Coexisting mineral pairs give an isotopic equilibration temperature range of 89?? to 163??C which overlaps with the 112?? to 198??C range obtained from primary fluid inclusions. Coexisting quartz has a ??18O value of 19 ?? 1 per mil (VSMOW). The fluid which deposited these minerals is inferred to have had ??18OH2o and ??34SH2s values of 5 ?? 1 and -1 ?? 1 per mil, respectively. Chemical and microthermometric analyses of fluid inclusions in quartz and sphalerite indicate salinities of 3 to 29 wt percent NaCl equiv with Na+ and Ca2+ as the dominant cations in solution. The Br/Cl and I/Cl ratios differ from those characteristic of magmatic waters and pristine seawater, but show some similarity to those observed in deep ground waters in crystalline terranes, basinal brines, and evaporated seawater, Barite, which postdates the sulfides, spans isotopic ranges of 13 to 21 per mil, 10 to 15 per mil, and 0.7109 to 0.7123 for ??34S, ??18O, and 87Sr/86Sr, respectively. The three parameters are correlated providing strong evidence that the barites are products of fluid mixing. We propose that the Cierco deposits formed along an extensional fault system at the margin of a marine basin during the breakup of Pangea at some time between the Early Triassic and Early Cretaceous. Sulfide deposition corresponded to an upwelling of hydrothermal fluid from the Paleozoic basement and was limited by the amount of metals carried by the fluid. Barite deposition corresponded to the waning of upward flow and the collapse of sulfate-rich surface waters onto the retreating hydrothermal plume. Calcite precipitated late in the paragenesis as meteoric or marine waters descended into the fault system

  18. Textural, compositional, and sulfur isotope variations of sulfide minerals in the Red Dog Zn-Pb-Ag deposits, Brooks Range, Alaska: Implications for Ore Formation

    USGS Publications Warehouse

    Kelley, K.D.; Leach, D.L.; Johnson, C.A.; Clark, J.L.; Fayek, M.; Slack, J.F.; Anderson, V.M.; Ayuso, R.A.; Ridley, W.I.

    2004-01-01

    The Red Dog Zn-Pb deposits are hosted in organic-rich mudstone and shale of the Mississippian Kuna Formation. A complex mineralization history is defined by four sphalerite types or stages: (1) early brown sphalerite, (2) yellow-brown sphalerite, (3) red-brown sphalerite, and (4) late tan sphalerite. Stages 2 and 3 constitute the main ore-forming event and are volumetrically the most important. Sulfides in stages 1 and 2 were deposited with barite, whereas stage 3 largely replaces barite. Distinct chemical differences exist among the different stages of sphalerite. From early brown sphalerite to later yellow-brown sphalerite and red-brown sphalerite, Fe and Co content generally increase and Mn and Tl content generally decrease. Early brown sphalerite contains no more than 1.9 wt percent Fe and 63 ppm Co, with high Mn (up to 37 ppm) and Tl (126 ppm), whereas yellow-brown sphalerite and red-brown sphalerite contain high Fe (up to 7.3 wt %) and Co (up to 382 ppm), and low Mn (<27 ppm) and Tl (<37 ppm). Late tan sphalerite has distinctly lower Fe (< 0.9 wt %) and higher Tl (up to 355 ppm), Mn (up to 177 ppm), and Ge (426 ppm), relative to earlier sphalerite. Wide ranges in concentrations of Ag, Cu, Pb, and Sb characterize all sphalerite types, particularly yellow-brown sphalerite and red-brown sphalerite, and most likely reflect submicroscopic inclusions of galena, chalcopyrite and/or tetrahedrite in the sphalerite. In situ ion microprobe sulfur isotope analyses show a progression from extremely low ??34S values for stage 1 (as low as -37.20???) to much higher values for yellow-brown sphalerite (mean of 3.3???; n = 30) and red-brown sphalerite (mean of 3.4; n = 20). Late tan sphalerite is isotopically light (-16.4 to -27.2???). The textural, chem ical, and isotopic data indicate the following paragenesis: (1) deposition of early brown sphalerite with abundant barite, minor pyrite, and trace galena immediately beneath the sea floor in unconsolidated mud; (2) deposition

  19. Influence of terminal acryloyl arms on the coordination chemistry of a ditopic pyrimidine-hydrazone ligand: comparison of Pb(II), Zn(II), Cu(II), and Ag(I) complexes.

    PubMed

    Hutchinson, Daniel J; Hanton, Lyall R; Moratti, Stephen C

    2013-03-01

    A new ditopic pyrimidine-hydrazone ligand, 6-hydroxymethylacryloyl-2-pyridinecarboxaldehyde, 2,2'-[2,2'-(2-methyl-4,6-pyrimidinediyl)bis(1-methylhydrazone)] (L2), was synthesized with terminal acryloyl functional groups to allow incorporation into copolymer gel actuators. NMR spectroscopy was used to show that L2 adopted a horseshoe shape with transoid-transoid pym-hyz-py linkages. Metal complexation studies were performed with L2 and salts of Pb(II), Zn(II), Cu(II), and Ag(I) ions in CH3CN in a variety of metal to ligand ratios. Reacting L2 with an excess amount of any of the metal ions resulted in linear complexes where the pym-hyz-py linkages were rotated to a cisoid-cisoid conformation. NMR spectroscopy showed that the acryloyl arms of L2 did not interact with the bound metal ions in solution. Seven of the linear complexes (1-7) were crystallized and analyzed by X-ray diffraction. Most of these complexes (4-7) also showed no coordination between the acryloyl arms and the metal ions; however, complexes 1-3 showed some interactions. Both of the acryloyl arms were coordinated to Pb(II) ions in [Pb2L2(SO3CF3)4] (1), one through the carbonyl oxygen donor and the other through the alkoxy oxygen donor. One of the acryloyl arms of [Cu2L2(CH3CN)3](SO3CF3)4 (2) was coordinated to one of the Cu(II) ions through the carbonyl oxygen donor. There appeared to be a weak association between the alkoxy donors of the acryloyl arms and the Pb(II) ions of [Pb2L2(ClO4)4]·CH3CN (3). Reaction of excess AgSO3CF3 with L2 was repeated in CD3NO2, resulting in crystals of {[Ag7(L2)2(SO3CF3)6(H2O)2] SO3CF3}∞ (8), the polymeric structure of which resulted from coordination between the carbonyl donors of the acryloyl arms and the Ag(I) ions. In all cases the coordination and steric effects of the acryloyl arms did not inhibit isomerization of the pym-hyz bonds of L2 or the core shape of the linear complexes.

  20. Genesis of the Assif El Mal Zn-Pb (Cu, Ag) vein deposit. An extension-related Mesozoic vein system in the High Atlas of Morocco. Structural, mineralogical, and geochemical evidence

    USGS Publications Warehouse

    Bouabdellah, M.; Beaudoin, G.; Leach, D.L.; Grandia, F.; Cardellach, E.

    2009-01-01

    The Assif El Mal Zn-Pb (Cu-Ag) vein system, located in the northern flank of the High Atlas of Marrakech (Morocco), is hosted in a Cambro-Ordovician volcaniclastic and metasedimentary sequence composed of graywacke, siltstone, pelite, and shale interlayered with minor tuff and mudstone. Intrusion of synorogenic to postorogenic Late Hercynian peraluminous granitoids has contact metamorphosed the host rocks giving rise to a metamorphic assemblage of quartz, plagioclase, biotite, muscovite, chlorite, amphibole, chloritoid, and garnet. The Assif El Mal Zn-Pb (Cu-Ag) mineralization forms subvertical veins with ribbon, fault breccia, cockade, comb, and crack and seal textures. Two-phase liquid-vapor fluid inclusions that were trapped during several stages occur in quartz and sphalerite. Primary inclusion fluids exhibit Th mean values ranging from 104??C to 198??C. Final ice-melting temperatures range from -8.1??C to -12.8??C, corresponding to salinities of ???15 wt.% NaCl equiv. Halogen data suggest that the salinity of the ore fluids was largely due to evaporation of seawater. Late secondary fluid inclusions have either Ca-rich, saline (26 wt.% NaCl equiv.), or very dilute (3.5 wt.% NaCl equiv.) compositions and homogenization temperatures ranging from 75??C to 150??C. The ??18O and ??D fluid values suggest an isotopically heterogeneous fluid source involving mixing between connate seawater and black-shale-derived organic waters. Low ??13CVPDB values ranging from -7.5??? to -7.7??? indicate a homogeneous carbon source, possibly organic matter disseminated in black shale hosting the Zn-Pb (Cu-Ag) veins. The calculated ??34SH2S values for reduced sulfur (22.5??? to 24.3???) are most likely from reduction of SO42- in trapped seawater sulfate or evaporite in the host rocks. Reduction of sulfate probably occurred through thermochemical sulfate reduction in which organic matter was oxidized to produce CO2 which ultimately led to precipitation of saddle dolomite with

  1. Genesis of the Assif El Mal Zn-Pb (Cu, Ag) vein deposit. An extension-related Mesozoic vein system in the High Atlas of Morocco. Structural, mineralogical, and geochemical evidence

    NASA Astrophysics Data System (ADS)

    Bouabdellah, Mohammed; Beaudoin, Georges; Leach, David L.; Grandia, Fidel; Cardellach, Esteve

    2009-08-01

    The Assif El Mal Zn-Pb (Cu-Ag) vein system, located in the northern flank of the High Atlas of Marrakech (Morocco), is hosted in a Cambro-Ordovician volcaniclastic and metasedimentary sequence composed of graywacke, siltstone, pelite, and shale interlayered with minor tuff and mudstone. Intrusion of synorogenic to postorogenic Late Hercynian peraluminous granitoids has contact metamorphosed the host rocks giving rise to a metamorphic assemblage of quartz, plagioclase, biotite, muscovite, chlorite, amphibole, chloritoid, and garnet. The Assif El Mal Zn-Pb (Cu-Ag) mineralization forms subvertical veins with ribbon, fault breccia, cockade, comb, and crack and seal textures. Two-phase liquid-vapor fluid inclusions that were trapped during several stages occur in quartz and sphalerite. Primary inclusion fluids exhibit T h mean values ranging from 104°C to 198°C. Final ice-melting temperatures range from -8.1°C to -12.8°C, corresponding to salinities of ˜15 wt.% NaCl equiv. Halogen data suggest that the salinity of the ore fluids was largely due to evaporation of seawater. Late secondary fluid inclusions have either Ca-rich, saline (26 wt.% NaCl equiv.), or very dilute (3.5 wt.% NaCl equiv.) compositions and homogenization temperatures ranging from 75°C to 150°C. The δ18O and δD fluid values suggest an isotopically heterogeneous fluid source involving mixing between connate seawater and black-shale-derived organic waters. Low δ13CVPDB values ranging from -7.5‰ to -7.7‰ indicate a homogeneous carbon source, possibly organic matter disseminated in black shale hosting the Zn-Pb (Cu-Ag) veins. The calculated δ34SH2S values for reduced sulfur (22.5‰ to 24.3‰) are most likely from reduction of SO4 2- in trapped seawater sulfate or evaporite in the host rocks. Reduction of sulfate probably occurred through thermochemical sulfate reduction in which organic matter was oxidized to produce CO2 which ultimately led to precipitation of saddle dolomite with

  2. A rapid, partial leach and organic separation for the sensitive determination of Ag, Bi, Cd, Cu, Mo, Pb, Sb, and Zn in surface geologic materials by flame atomic absorption

    USGS Publications Warehouse

    Viets, J.G.; Clark, J.R.; Campbell, W.L.

    1984-01-01

    A solution of dilute hydrochloric acid, ascorbic acid, and potassium iodide has been found to dissolve weakly bound metals in soils, stream sediments, and oxidized rocks. Silver, Bi, Cd, Cu, Mo, Pb, Sb, and Zn are selectively extracted from this solution by a mixture of Aliquat 336 (tricaprylyl methyl ammonium chloride) and MIBK (methyl isobutyl ketone). Because potentially interfering major and minor elements do not extract, the organic separation allows interference-free determinations of Ag and Cd to the 0.05 ppm level, Mo, Cu, and Zn to 0.5 ppm, and Bi, Pb, and Sb to 1 ppm in the sample using flame atomic absorption spectroscopy. The analytical absorbance values of the organic solution used in the proposed method are generally enhanced more than threefold as compared to aqueous solutions, due to more efficient atomization and burning characteristics. The leaching and extraction procedures are extremely rapid; as many as 100 samples may be analyzed per day, yielding 800 determinations, and the technique is adaptable to field use. The proposed method was compared to total digestion methods for geochemical reference samples as well as soils and stream sediments from mineralized and unmineralized areas. The partial leach showed better anomaly contrasts than did total digestions. Because the proposed method is very rapid and is sensitive to pathfinder elements for several types of ore deposits, it should be useful for reconnaissance surveys for concealed deposits. ?? 1984.

  3. Effects of temperature, silicate melt composition, and oxygen fugacity on the partitioning of V, Mn, Co, Ni, Cu, Zn, As, Mo, Ag, Sn, Sb, W, Au, Pb, and Bi between sulfide phases and silicate melt

    NASA Astrophysics Data System (ADS)

    Li, Yuan; Audétat, Andreas

    2015-08-01

    In order to assess the role of sulfide in controlling the ore metal budgets and fractionation during magmatic genesis and differentiation, the partition coefficients (D) of V, Mn, Co, Ni, Cu, Zn, As, Mo, Ag, Sn, Sb, W, Au, Pb, and Bi between sulfide liquid (SL), monosulfide solid solution (MSS), and basaltic to rhyolitic melts (SM) were determined at 900-1200 °C, 0.5-1.5 GPa, and oxygen fugacity (fO2) ranging from ∼FMQ-2 to FMQ+3, in a piston-cylinder apparatus. The DSL/SM values range from 0.4 to 2 for V, 0.5 to 3 for Mn, 80 to 580 for Co, 2300 to 18,000 for Ni, 800 to 4600 for Cu, 1 to 11 for Zn, 20 to 180 for As, 4 to 230 for Mo, 450 to 1600 for Ag, 5 to 24 for Sn, 10 to 80 for Sb, 0.03 to 0.16 for W, 2000 to 29,000 for Au, 24 to 170 for Pb, and 830 to 11,000 for Bi; whereas the DMSS/SM values range from 0.04 to 10 for V, 0.5 to 10 for Mn, 70 to 2500 for Co, 650 to 18,000 for Ni, 280 to 42,000 for Cu, 0.1 to 80 for Zn, 0.2 to 30 for As, 1 to 820 for Mo, 20 to 500 for Ag, 0.2 to 220 for Sn, 0.1 to 40 for Sb, 0.01 to 24 for W, 10 to 2000 for Au, 0.03 to 6 for Pb, and 1 to 350 for Bi. Both DMSS/SM and DSL/SM values generally increase with decreasing temperature or decreasing FeOtot content in silicate melt, except for Mo, DMSS/SM and DSL/SM of which show a clear decrease with decreasing temperature. At given temperature and FeOtot content, high oxygen fugacity appears to lead to a significant decrease in DMSS/SM of Au, Bi, Mo, and potentially As. The partitioning data obtained experimentally in this study and previous studies were fitted to an empirical equation that expresses the DMSS/SM and/or DSL/SM of a given element as a function of temperature, oxygen fugacity, and FeOtot content of the silicate melt: log (DSL/SMorDMSS/SM = d + a · 10, 000 / T + b · (ΔFMQ) + c · log (FeOmelt) in which T is temperature in K, FeOmelt denotes wt% FeOtot in silicate melt, and ΔFMQ denotes log fO2 relative to the fayalite-magnetite-quartz (FMQ) oxygen buffer. The

  4. Impacts of anthropogenic pressures on the water quality of the Gironde Estuary (SW France) from the Urban Agglomeration of Bordeaux: spatial characterization and inputs of trace metal elements (Ag, As, Cd, Cu, Pb and Zn)

    NASA Astrophysics Data System (ADS)

    Kessaci, Kahina; Coynel, Alexandra; Blanc, Gérard; Deycard, Victoria N.; Derriennic, Hervé; Schäfer, Jörg

    2014-05-01

    Recent European legislation (2000/60/CE) has listed eight trace metal elements as priority toxic substances for water quality. Urban metal inputs into hydrosystems are of increasing interest to both scientists and managers facing restrictive environmental protection policies, population increase and changing metal applications. The Gironde Estuary (SW France; 625 km2) is known for its metal/metalloid pollution originating from industrial (e.g. Cd, Zn, Cu, As, Ag, Hg) or agricultural sources (e.g. Cu) in the main fluvial tributaries (Garonne and Dordogne Rivers). However, little peer-reviewed scientific work has addressed the impact of urban sources on the Gironde Estuary, especially the Urban Agglomeration of Bordeaux (~1 million inhabitants) located on the downstream branch of the Garonne River. In this study, a snapshot sampling campaign was performed in 2011 for characterizing the spatial distribution of dissolved and particulate metal/metalloid (As, Ag, Cd, Pb, Zn, Cu) concentrations in three suburban watersheds: the Jalle of Blanquefort (330 km2), Eau Bourde (140 km2), and Peugue (112 km2). Furthermore, particulate metal Enrichment Factors (EF) were calculated using local geochemical background measured at the bottom of a sediment core (492 cm). Results indicated that metal concentrations displayed a high spatial variability depending on the suburban watershed and the studied element. Local concentrations anomalies were observed for: (i) As in the Eau Bourde River in dissolved (4.2 μg/l) and particulate phases (246 mg/kg; EF= 20) and attributed to a nearby industrial incinerator; (ii) Zn in the Peugue River with maximum dissolved and particulate concentrations of 87 μg/l and 1580 mg/kg (EF=17), respectively, probably due to urban habitation runoff; (iii) Ag in the Jalle of Blanquefort River with high dissolved (74 ng/l) and particulate concentrations (33.7 mg/kg; EF=117) due to industrial activities in the downstream part. Based on hydro

  5. Partitioning of V, Mn, Co, Ni, Cu, Zn, As, Mo, Ag, Sn, Sb, W, Au, Pb, and Bi between sulfide phases and hydrous basanite melt at upper mantle conditions

    NASA Astrophysics Data System (ADS)

    Li, Yuan; Audétat, Andreas

    2012-11-01

    The partitioning of 15 major to trace metals between monosulfide solid solution (MSS), sulfide liquid (SL) and mafic silicate melt (SM) was determined in piston-cylinder experiments performed at 1175-1300 °C, 1.5-3.0 GPa and oxygen fugacities ranging from 3.1 log units below to 1.0 log units above the quartz-fayalite-magnetite fO2 buffer, which conditions are representative of partial melting in the upper mantle in different tectonic settings. The silicate melt was produced by partial melting of a natural, amphibole-rich mantle source rock, resulting in hydrous (˜5 wt% H2O) basanitic melts similar to low-degree partial melts of metasomatized mantle, whereas the major element composition of the starting sulfide (˜52 wt% Fe; 39 wt% S; 7 wt% Ni; 2 wt% Cu) was similar to the average composition of sulfides in this environment. SL/SM partition coefficients are high (≥100) for Au, Ni, Cu, Ag, Bi, intermediate (1-100) for Co, Pb, Sn, Sb (±As, Mo), and low (≤1) for the remaining elements. MSS/SM partition coefficients are generally lower than SL/SM partition coefficients and are high (≥100) for Ni, Cu, Au, intermediate (1-100) for Co, Ag (±Bi, Mo), and low (≤1) for the remaining elements. Most sulfide-silicate melt partition coefficients vary as a function of fO2, with Mo, Bi, As (±W) varying by a factor >10 over the investigated fO2 range, Sb, Ag, Sn (±V) varying by a factor of 3-10, and Pb, Cu, Ni, Co, Au, Zn, Mn varying by a factor of 3-10. The partitioning data were used to model the behavior of Cu, Au, Ag, and Bi during partial melting of upper mantle and during fractional crystallization of primitive MORB and arc magmas. Sulfide phase relationships and comparison of the modeling results with reported Cu, Au, Ag, and Bi concentrations from MORB and arc magmas suggest that: (i) MSS is the dominant sulfide in the source region of arc magmas, and thus that Au/Cu ratios in the silicate melt and residual sulfides may decrease with increasing degree of

  6. Geologic, geochemical, and isotopic studies of a carbonate- and siliciclastic-hosted Pb-Zn deposit at Lion Hill, Vermont

    USGS Publications Warehouse

    Foley, Nora K.; Clark, Sandra H.B.; Woodruff, Laurel G.; Mosier, Elwin L.

    1995-01-01

    The prospect of an Irish-type sedimentary-exhalative origin for stratabound Pb-Zn deposits of the Paleozoic shelf of North America is of considerable importance to understanding the timing of mineralization relative to platform evolution and for evaluating the mineral resource potential of the region. Our study of the Lion Hill deposit indicates a potential for Irish-type Pb-Zn deposits in platform rocks of western Vermont; however, at Lion Hill they contain enrichments of Pb, Zn, and Cu rather than a Pb, Zn, and Ag association.

  7. Bipolar Ag-Zn battery

    NASA Technical Reports Server (NTRS)

    Giltner, L. John

    1994-01-01

    The silver-zinc (AgZn) battery system has been unique in its ability to safely satisfy high power demand applications with low mass and volume. However, a new generation of defense, aerospace, and commercial applications will impose even higher power demands. These new power demands can be satisfied by the development of a bipolar battery design. In this configuration the power consuming, interelectrode current conductors are eliminated while the current is then conducted via the large cross-section electrode substrate. Negative and positive active materials are applied to opposite sides of a solid silver foil substrate. In addition to reducing the weight and volume required for a specified power level, the output voltage performance is also improved as follows. Reduced weight through: elimination of the plastic cell container; elimination of plate leads and intercell connector; and elimination of internal plate current collector. Increased voltage through: elimination of resistance of current collector; elimination of resistance of plate lead; and elimination of resistance of intercell connector. EPI worked previously on development of a secondary bipolar silver zinc battery. This development demonstrated the electrical capability of the system and manufacturing techniques. One difficulty with this development was mechanical problems with the seals. However, recent improvements in plastics and adhesives should eliminate the major problem of maintaining a seal around the periphery of the bipolar module. The seal problem is not as significant for a primary battery application or for a requirement for only a few discharge cycles. A second difficulty encountered was with activation (introducing electrolyte into the cell) and with venting gas from the cell without loss of electrolyte. During previous work, the following projections for energy density were made from test data for a high power system which demonstrated in excess of 50 discharge/charge cycles. Projected

  8. 3D modelling and sheath folding at the Falun pyritic Zn-Pb-Cu-(Au-Ag) sulphide deposit and implications for exploration in a 1.9 Ga ore district, Fennoscandian Shield, Sweden

    NASA Astrophysics Data System (ADS)

    Kampmann, Tobias C.; Stephens, Michael B.; Weihed, Pär

    2016-06-01

    Altered and mineralized rocks at the Falun pyritic Zn-Pb-Cu-(Au-Ag) sulphide deposit, situated in the Palaeoproterozoic Bergslagen ore district in the south-western part of the Fennoscandian Shield, have been metamorphosed at low-pressure, amphibolite-facies conditions and affected by ductile deformation. Using combined surface mapping of lithology and structure, drill core logging and microstructural work, the polyphase (D1 and D2) ductile deformation is demonstrated and a 3D model for the deposit created. Mineral associations include quartz, biotite, cordierite, anthophyllite, and minor almandine, andalusite and chlorite in silicate-rich altered rock, calcite or dolomite in marble and tremolite-actinolite or diopside-hedenbergite in skarn. The silicate minerals show varying growth patterns during the different phases of the tectonothermal evolution, with considerable static grain growth occurring between D1 and D2, and even after D2. F2 sheath folding along axes that plunge steeply to the SSE, parallel to a mineral stretching lineation and the dip direction of the S2 foliation, is suggested as a key deformation mechanism forming steeply plunging, cone- to rod-shaped mineralized bodies. This contrasts with a previous structural model invoking fold interference. A major shear zone with talc-chlorite-(quartz-biotite) mineral association separates the northern and southern structural domains at the deposit and bounds the polymetallic massive sulphides to the north.

  9. Bitumen II from the Paleoproterozoic Here’s Your Chance Pb/Zn/Ag deposit: Implications for the analysis of depositional environment and thermal maturity of hydrothermally-altered sediments

    NASA Astrophysics Data System (ADS)

    Holman, Alex I.; Grice, Kliti; Jaraula, Caroline M. B.; Schimmelmann, Arndt

    2014-08-01

    The formation of sedimentary exhalative (SEDEX) Pb/Zn deposits is linked to ocean euxinia, but recent evidence suggests that ferruginous conditions may have dominated the deep ocean during the Middle Proterozoic, a maximum period for SEDEX distribution. Biomarkers of sulfate-reducing and sulfide-oxidising bacteria are valuable indicators of euxinic conditions in such settings. Organic matter (OM) from SEDEX deposits is often affected by alteration and/or migration, but OM entrapped within the kerogen/mineral matrix (Bitumen II) may be less affected than the freely-extractable OM (Bitumen I). We analysed Bitumen II from the Paleoproterozoic Here’s Your Chance (HYC) Pb/Zn/Ag deposit to find evidence of euxinic conditions in the depositional environment. n-Alkane distributions in Bitumen II are markedly distinct from previously-reported Bitumen I. Bitumen II contains long-chain n-alkanes (up to C36 or C38) and a strong even-over-odd distribution in a number of samples, which are 4‰ to 7‰ depleted in 13C compared to n-alkanes in Bitumen I and verified as indigenous by comparison with δ13C of isolated kerogen. These features are interpreted as evidence of sulfate-reducing and sulfide-oxidising bacteria, confirming that HYC was deposited under euxinic conditions. Bitumen II has the potential to reveal information from OM that is degraded and/or overprinted in Bitumen I. Commonly-used methylphenanthrene maturity ratios give conflicting information as to the relative maturity of Bitumens I and II. Bitumen I contains a far higher proportion of methylated phenanthrenes than Bitumen II. As Bitumen II is sequestered within the kerogen/mineral matrix it may have restricted access to the ‘methyl pool’ of organic compounds that can donate methyl groups to aromatic hydrocarbons. Parameters that include both phenanthrene and methylphenanthrenes do not appear suitable to compare the maturity of Bitumens I and II; hence there is no clear evidence that Bitumen II is of

  10. Ag-ZnO nanostructure for ANTA explosive molecule detection

    NASA Astrophysics Data System (ADS)

    Shaik, Ummar Pasha; Sangani, L. D. Varma; Gaur, Anshu; Mohiddon, Md. Ahamad; Krishna, M. Ghanashyam

    2016-05-01

    Ag/ZnO nanostructure for surface enhanced Raman scattering application in the detection of ANTA explosive molecule is demonstrated. A highly rough ZnO microstructure was achieved by rapid thermal annealing of metallic Zn film. Different thickness Ag nanostructures are decorated over these ZnO microstructures by ion beam sputtering technique. Surface enhanced Raman spectroscopic studies carried out over Ag/ZnO substrates have shown three orders higher enhancement compared to bare Ag nanostructure deposited on the same substrate. The reasons behind such huge enhancement are discussed based on the morphology of the sample.

  11. Genesis of the Bangbule Pb-Zn-Cu polymetallic deposit in Tibet, western China: Evidence from zircon U-Pb geochronology and S-Pb isotopes

    NASA Astrophysics Data System (ADS)

    Kan, Tian; Zheng, Youye; Gao, Shunbao

    2016-04-01

    The Banbule Pb-Zn-Cu skarn deposit is located in the Longger-Gongbujiangda volcanic magma arc in the Gangdese-Nyainqentanglha Plate. It is the only lead-zinc polymetallic deposit discovered in the westernmost Nyainqentanglha metallogenic belt. The measured and indicated resources include 0.9 Mt of Pb+Zn (4.77% Pb and 4.74% Zn, respectively), 6499 t of Cu, and 178 t of Ag (18.75g/t Ag). The orebodies mainly occur as lenses, veins and irregular shapes in the contact zone between the quartz-porphyry and limestone of the Upper Permian Xiala Formation, or in the boundaries between limestone and sandstone. Pb-Zn-Cu mineralization in the Banbule deposit is closely associated with skarns. The ore minerals are dominated by galena, sphalerite, chalcopyrite, bornite, and magnetite, with subordinate pyrite, malachite, and azurite. The gangue minerals are mainly garnet, actinolite, diopside, quartz, and calcite. The ore-related quartz-porphyry displays LA-ICP-MS zircon U-Pb age of 77.31±0.74 Ma. The δ34S values of sulfides define a narrow range of -0.8 to 4.7‰ indicating a magmatic source for the ore-forming materials. Lead isotopic systematics yield 206Pb/204Pb of 18.698 to 18.752, 207Pb/204Pb of 15.696 to 15.760, and 208Pb/204Pb of 39.097 to 39.320. The data points are constrained around the growth curves of upper crust and orogenic belt according to the tectonic discrimination diagrams. The calculated Δβ - Δγ values plot within the magmatic field according to the discrimination diagram of Zhu et al. (1995). The S-Pb isotopic data suggest that Bangbule is a typical skarn deposit, and the Pb-Zn-Cu mineralization is genetically related to the quartz-porphyry in the mining district. The discovery of the Bangbule deposit indicates that there is metallogenic potential in the westernmost Nyainqentanglha belt, which is of great importance for the exploration work in this area.

  12. Genesis of the Bangbule Pb-Zn-Cu polymetallic deposit in Tibet, western China: Evidence from zircon U-Pb geochronology and S-Pb isotopes

    NASA Astrophysics Data System (ADS)

    Kan, Tian; Zheng, Youye; Gao, Shunbao

    2016-04-01

    The Banbule Pb-Zn-Cu skarn deposit is located in the Longger-Gongbujiangda volcanic magma arc in the Gangdese-Nyainqentanglha Plate. It is the only lead-zinc polymetallic deposit discovered in the westernmost Nyainqentanglha metallogenic belt. The measured and indicated resources include 0.9 Mt of Pb+Zn (4.77% Pb and 4.74% Zn, respectively), 6499 t of Cu, and 178 t of Ag (18.75g/t Ag). The orebodies mainly occur as lenses, veins and irregular shapes in the contact zone between the quartz-porphyry and limestone of the Upper Permian Xiala Formation, or in the boundaries between limestone and sandstone. Pb-Zn-Cu mineralization in the Banbule deposit is closely associated with skarns. The ore minerals are dominated by galena, sphalerite, chalcopyrite, bornite, and magnetite, with subordinate pyrite, malachite, and azurite. The gangue minerals are mainly garnet, actinolite, diopside, quartz, and calcite. The ore-related quartz-porphyry displays LA-ICP-MS zircon U-Pb age of 77.31±0.74 Ma. The δ34S values of sulfides define a narrow range of -0.8 to 4.7‰ indicating a magmatic source for the ore-forming materials. Lead isotopic systematics yield 206Pb/204Pb of 18.698 to 18.752, 207Pb/204Pb of 15.696 to 15.760, and 208Pb/204Pb of 39.097 to 39.320. The data points are constrained around the growth curves of upper crust and orogenic belt according to the tectonic discrimination diagrams. The calculated Δβ ‑ Δγ values plot within the magmatic field according to the discrimination diagram of Zhu et al. (1995). The S-Pb isotopic data suggest that Bangbule is a typical skarn deposit, and the Pb-Zn-Cu mineralization is genetically related to the quartz-porphyry in the mining district. The discovery of the Bangbule deposit indicates that there is metallogenic potential in the westernmost Nyainqentanglha belt, which is of great importance for the exploration work in this area.

  13. Distinguishing regional- and local-scale metasomatic systems at the Prairie Downs Zn-Pb deposit

    NASA Astrophysics Data System (ADS)

    White, Alistair J. R.; Pearce, Mark A.; Meadows, Holly R.

    2016-10-01

    Geochemical alteration in mafic rocks of the Fortescue Group around the Prairie Downs Zn-Pb-(Cu-Ag) deposit, Western Australia, is the result of two overprinting metasomatic systems. The first, a regional-scale event, well documented across the Fortescue Basin to the north, resulted in extensive depletion in alkalis, Mg, and heavier first transition series metals (Mn-Zn), and formation of mineral assemblages progressing towards pure epidote/pumpellyite-quartz end-members. The second, more localised event, was associated with Zn-Pb-(Cu-Ag) mineralisation and resulted in Ca-loss accompanied by enrichment in a broad transition metal and metalloid suite (Zn-Pb-Sn-Ag-K-Ba-Tl-Sb-Ge-U-Th-Cd-Hg-Se-REE) that is comparable to many sedimentary exhalative (SEDEX) systems, and possibly represents modification or remobilisation of an earlier ore system. The mineralisation-related alteration was superimposed on the earlier regional-scale metasomatism: previously unaltered basalts underwent Zn-bearing chlorite and biotite growth, with loss of amphibole and epidote; regionally metasomatised rocks now comprise assemblages dominated by quartz, muscovite and baileychlore (Zn chlorite). These altered basalts do not contain any sulphide minerals and all Zn is hosted within chlorite in a broad halo around the main sulphide zones, thereby providing a larger exploration target. Geochemical modelling with HCh indicates that the observed alteration assemblages can be generated through interaction of rocks with large volumes of a saline, Zn-K-bearing fluid (fluid/rock ~ 1000). This study highlights the importance of understanding the regional geochemical background when investigating local metasomatic systems in order to correctly characterise them, determine their origin and position in a regional tectonic framework, and to correctly identify vectors towards mineralisation to aid future exploration.

  14. Hydrogen in Ag-doped ZnO: theoretical calculations.

    PubMed

    He, H Y; Hu, J; Pan, B C

    2009-05-28

    Based on density functional theory calculations, we systematically investigate the behaviors of a H atom in Ag-doped ZnO involving the preference sites, diffusion behaviors, the electronic structures, and vibrational properties. We find that a H atom can migrate to the doped Ag to form a Ag-H complex by overcoming energy barriers of 0.3-1.0 eV. The lowest-energy site for H location is the bond center of a Ag-O in the basal plane. Moreover, H can migrate between this site and its equivalent sites with energy cost of less than 0.5 eV. In contrast, dissociation of such a Ag-H complex needs energy of about 1.1-1.3 eV. This implies that the Ag-H complexes can commonly exist in the Ag-doped ZnO, which have a negative effect on the desirable p-type carrier concentrations of Ag-doped ZnO. In addition, based on the frozen phonon calculation, the vibrational properties of ZnO with a Ag-H complex are predicted. Some new vibrational modes associated with the Ag-H complex present in the vibrational spectrum of the system.

  15. Systematics of hydrothermal alteration at the volcanic-hosted Falun Zn-Pb-Cu-(Au-Ag) deposit - implications for ore genesis, structure and exploration in a 1.9 Ga ore district, Fennoscandian Shield, Sweden

    NASA Astrophysics Data System (ADS)

    Kampmann, Tobias C.; Jansson, Nils J.; Stephens, Michael B.; Majka, Jarosław

    2016-04-01

    The Palaeoproterozoic, volcanic-hosted Falun Zn-Pb-Cu-(Au-Ag) sulphide deposit was mined for base and precious metals during several centuries, until its closure in 1992. The deposit is located in a 1.9 Ga ore district in the Bergslagen lithotectonic unit, Fennoscandian Shield, south-central Sweden. Both the ores and their host rock underwent polyphase ductile deformation, and metamorphism under amphibolite facies and later retrograde conditions at 1.9-1.8 Ga (Svecokarelian orogenic system). This study has the following aims: (i) Classify styles and intensities of alteration in the hydrothermally altered zone at Falun; (ii) identify precursor rocks to hydrothermally altered rocks and their spatial distribution at the deposit; (iii) evaluate the chemical changes resulting from hydrothermal alteration using mass change calculations; and (iv) assess the pre-metamorphic alteration assemblages accounting for the observed metamorphic mineral associations in the altered rocks at Falun. Results will have implications for both the ore-genetic and structural understanding of the deposit, as well as for local and regional exploration. Metamorphic mineral associations in the altered rocks include biotite-quartz-cordierite-(anthophyllite) and, more proximally, quartz-anthophyllite-(biotite-cordierite/almandine), biotite-cordierite-(anthophyllite) and biotite-almandine-(anthophyllite). The proximal hydrothermally altered zone corresponds to intense chlorite-style alteration. Subordinate dolomite or calcite marble, as well as calc-silicate (tremolite, diopside) rocks are also present at the deposit. Metavolcanic rocks around the deposit are unaltered, weakly sericitized or sodic-altered. Immobile-element (e.g. Zr, TiO2, Al2O3, REE) systematics of the silicate-rich samples at and around the deposit suggest that the precursors to the hydrothermally altered rocks at Falun were predominantly rhyolitic in composition, dacitic rocks being subordinate and mafic-intermediate rocks

  16. Sulphide and supergene nonsulphide Zn-Pb deposits of the southern Kootenay Arc, British Columbia, Canada

    NASA Astrophysics Data System (ADS)

    Paradis, S.; Simandl, G. J.

    2009-05-01

    The Kootenay Arc (KA) hosts a large number of carbonate-hosted base metal (Zn-Pb) deposits. These deposits occur mainly within the dolomitized limestone of the Lower Cambrian Badshot Formation (or its equivalent the Reeves Member of the Laib Formation), and the Upper Cambrian to Lower Ordovician Nelway Formation. They range in size from 6-10 million tonnes with average grades of 3-4% Zn, 1-2% Pb, 0.4% Cd and traces of Ag. The deposits, their dolomitic envelopes, and the limestone hostrock lie within secondary isoclinal folds along the limbs of regional anticlinal structures. Most of the deposits are stratabound lenticular concentrations of sphalerite, galena, pyrite, local pyrrhotite and rare arsenopyrite in isoclinally folded dolomitized or silicified carbonate layers. Brecciated zones are common within the more massive sulphide mineralization. Several deposits are past producers (e.g., Reeves MacDonald, Jersey, and HB) and others are advanced prospects. They are interpreted as metamorphosed MVT- or Irish-type Pb-Zn deposits. The main concentrations of these deposits define the Salmo and Duncan camps. The near-surface portions of these carbonate-hosted sulphide deposits are weathered and strongly oxidized (supergene environment). They consist of extensive Zn- and Pb-bearing iron oxide gossans and base metal-bearing nonsulphide mineralization. The most common nonsulphide minerals are goethite, hematite, hemimorphite, smithsonite, cerussite, anglesite, and hydrozincite. The Reeves MacDonald, Jersey-Emerald, Lomond, and Oxide group of deposits are the best examples of carbonate-hosted nonsulphide base metal (CHNSBM) deposits in the KA. The shape, mineralogy and paragenesis of the known CHNSBM deposits are indicative of direct-replacement of sulphides by nonsulphide base metal-bearing minerals. Zn-rich (low Pb) CHNSBM deposits commonly form by interaction of Zn-rich fluids with carbonate wallrock (replacement process). Such deposits (consisting of "white ore") may

  17. Photoluminescence study of ZnS and ZnS:Pb nanoparticles

    SciTech Connect

    Virpal, Hastir, Anita; Kaur, Jasmeet; Singh, Gurpreet; Singh, Ravi Chand

    2015-05-15

    Photoluminescence (PL) study of pure and 5wt. % lead doped ZnS prepared by co-precipitation method was conducted at room temperature. The prepared nanoparticles were characterized by X-ray Diffraction (XRD), UV-Visible (UV-Vis) spectrophotometer, Photoluminescence (PL) and Raman spectroscopy. XRD patterns confirm cubic structure of ZnS and PbS in doped sample. The band gap energy value increased in case of Pb doped ZnS nanoparticles. The PL spectrum of pure ZnS was de-convoluted into two peaks centered at 399nm and 441nm which were attributed to defect states of ZnS. In doped sample, a shoulder peak at 389nm and a broad peak centered at 505nm were observed. This broad green emission peak originated due to Pb activated ZnS states.

  18. Pb-free Sn-Ag-Cu ternary eutectic solder

    DOEpatents

    Anderson, Iver E.; Yost, Frederick G.; Smith, John F.; Miller, Chad M.; Terpstra, Robert L.

    1996-06-18

    A Pb-free solder includes a ternary eutectic composition consisting essentially of about 93.6 weight % Sn-about 4.7 weight % Ag-about 1.7 weight % Cu having a eutectic melting temperature of about 217.degree. C. and variants of the ternary composition wherein the relative concentrations of Sn, Ag, and Cu deviate from the ternary eutectic composition to provide a controlled melting temperature range (liquid-solid "mushy" zone) relative to the eutectic melting temperature (e.g. up to 15.degree. C. above the eutectic melting temperature).

  19. Pb-free Sn-Ag-Cu ternary eutectic solder

    DOEpatents

    Anderson, I.E.; Yost, F.G.; Smith, J.F.; Miller, C.M.; Terpstra, R.L.

    1996-06-18

    A Pb-free solder includes a ternary eutectic composition consisting essentially of about 93.6 weight % Sn-about 4.7 weight % Ag-about 1.7 weight % Cu having a eutectic melting temperature of about 217 C and variants of the ternary composition wherein the relative concentrations of Sn, Ag, and Cu deviate from the ternary eutectic composition to provide a controlled melting temperature range (liquid-solid ``mushy`` zone) relative to the eutectic melting temperature (e.g. up to 15 C above the eutectic melting temperature). 5 figs.

  20. Ab inito study of Ag-related defects in ZnO

    NASA Astrophysics Data System (ADS)

    Wan, Qixin; Xiong, Zhihua; Li, Dongmei; Liu, Guodong

    2008-12-01

    Using first-principles calculations, we investigated the structure and electronic properties of Ag-related defects in ZnO. The calculation results indicate that AgZn behaves as acceptor. Simultaneously, by comparing the formation energy and electronic structure of Ag-related defects in ZnO, Oi-AgZn behaves as acceptor in Ag-doped ZnO and it is better to gain p-type ZnO. However, Hi-AgZn complex has the lowest formation energy. Thus, the formation of the other point defects is greatly suppressed by the formation of Hi in Ag-doped ZnO. Moreover, the H atoms can be easily dissociated from hydrogen-passivated complexes by post-annealing at moderate temperatures, thus, codoping Ag with H may be a good method to achieve p-type in Ag-doped ZnO.

  1. Enhanced Raman scattering and photocatalytic activity of Ag/ZnO heterojunction nanocrystals.

    PubMed

    Chen, Chongqi; Zheng, Yuanhui; Zhan, Yingying; Lin, Xingyi; Zheng, Qi; Wei, Kemei

    2011-10-01

    In this work, we study the enhancement of Raman signals and photocatalytic activity of Ag/ZnO heterojunctions with an Ag content of 1 at.%, which were synthesized by photochemical deposition of Ag nanoparticles onto pre-synthesized ZnO nanorods. A strong interaction between Ag and ZnO nanocrystals were evidenced by XPS and UV-vis spectroscopy. The binding energy of Ag nanoparticles shifts toward lower energy compared to that of pure Ag nanoparticles, revealing that electrons transfer from Ag to the ZnO nanocrystals. The red shift of the plasmon absorption peak of Ag nanoparticles in Ag/ZnO heterojunctions further confirms the strong interaction between the two components. This strong interaction, arising from the coupling between Ag and ZnO nanocrystals, is responsible for the enhancement of Raman signals and photocatalytic activity of the Ag/ZnO heterojunctions. PMID:21847472

  2. Sediment-hosted Pb-Zn Deposits: a global perspective

    USGS Publications Warehouse

    Leach, David L.; Sangster, Donald F.; Kelley, Karen D.; Large, R; Garven, G.; Allen, Craig R.

    2005-01-01

    Sediment-hosted Pb-Zn deposits contain the world's greatest lead and zinc resources and dominate world production of these metals. They are a chverse group of ore deposits hosted by a wide variety of carbonate and siliciclastic roch that have no obviolls genetic association with igneous activity. A nmge of ore-fortl1ing processes in a vmiety of geologic and tectonic environments created these deposits over at least two billion years of Earth history. The metals were precipitated by basinal brines in synsedimentary and early diagenetic to low-grade metamorphic environments. The deposits display a broad range of relationships to enclosing host rocks that includes stratiform, strata-bound, and discordant ores. These ores are divided into two broad subt)1Jes: Mississippi Valley-type (MVT) and sedimentmy exhalative (SEDEX), Despite the "exhalative" component inherent in the term "SEDEX," in this manusclipt, direct evidence of an exhalite in the ore or alteration component is not essential for a deposit to be classified as SEDEX. The presence of laminated sulfides parallel to bedding is assumed to be permissive evidence for exhalative ores. The chstinction between some SEDEX and MVT depOSits can be quite subjective because some SEDEX ores replaced carbonate, whereas some MVT depOSits formed in an early diagenetic environment and display laminated ore textures. Geologic and resource information are presented for 248 depositS that provide a framework to describe ,mel compare these deposits. Nine of tlle 10 largest sediment-hosted Pb-Zn deposits are SEDEX, Of the deposits that contain at least 2.5 million metric tons (Mt), there are 35 SEDEX (excluding Broken Hill-type) deposits and 15 MVT (excluding Iris-type) deposits. Despite the skewed distribution of the deposit size, the two deposits types have an excellent correlation between total tonnage and tonnage of contained metal (Pb + Zn), with a fairly consistent ratio of about lO/l, regardless of the size of the deposit or

  3. Theoretical and experimental investigation of stability and spectra of doped Ag:ZnSe nanocrystals.

    PubMed

    Xu, Shuhong; Wang, Chunlei; Wang, Zhuyuan; Cui, Yiping

    2014-04-01

    In experiment, doped Ag:ZnSe nanocrystals (NCs) had better stability than that of ZnSe nanocrystals under ambient atmospheres in the presence of air and light illumination. However, it is difficult to explain the mechanism of better stability of Ag:ZnSe nanocrystals from the experiment perspective for doped nanocrystals are more unstable than corresponding pure nanocrystals in general. Using B3LYP/LANL2DZ method, we have investigated the geometrical structures, bonding characters, and molecular orbitals (MOs) of hexagonal and tetrahedral Ag doped ZnSe structures in theory. The results showed that the good stability of Ag:ZnSe nanocrystals can be attributed to the stronger binding between Ag and Se. Moreover, we have proved that Ag doped ZnSe nanocrystals synthesized in experiment should be substituting doped but not vacuity doped. Substituting Ag doped ZnSe molecules have the same configuration as that of the ZnSe structure, but vacuity doped Ag:ZnSe have completely different configuration than ZnSe structure due to the big size of Ag atom. In addition, through contrast of MO of ZnSe and Ag doped ZnSe, we have testified that Ag easily formed bonds with Se. The high binding energy and high probability of forming bonds with Se atom make Ag doped ZnSe nanocrystals have better stability than that of ZnSe nanocrystals. PMID:24633779

  4. Luminescent and structural properties of ZnO-Ag films

    SciTech Connect

    Khomchenko, V. S. Kushnirenko, V. I. Papusha, V. P.; Savin, A. K.; Lytvyn, O. S.

    2010-05-15

    ZnO-Ag thin films were prepared by a two-stage method on glass and sapphire substrates. Ag doping was carried out by a method of close space sublimation at atmospheric pressure. The film thickness is varied from 0.6 to 7 {mu}m. The structural and radiative properties were explored by X-ray diffraction technique, atomic force microscopy, photoluminescence and cathodoluminescence spectroscopy. The influence of the fabricating conditions on the properties of ZnO-Ag films is studied. It is found that the Ag doping modifies the crystalline structure of the films and promotes the oriented growth of monocrystalline blocks with the size of 500-2000 nm in the [0002] direction. Improvement of the crystalline quality correlates with the change of the radiative characteristics of the films. The origin of emission centers is discussed.

  5. Geogenic and Anthropogenic Moss Responsiveness to Element Distribution Around a Pb-Zn Mine, Toranica, Republic of Macedonia.

    PubMed

    Angelovska, Svetlana; Stafilov, Trajče; Šajn, Robert; Balabanova, Biljana

    2016-04-01

    Moss species (Homalothecium lutescens, Hypnum cupressiforme, Brachythecium glareosum, and Campthotecium lutescens) were used as suitable sampling media for biomonitoring the origin of heavy-metal pollution in the lead-zinc (Pb-Zn) mine "Toranica" near the Kriva Palanka town, Eastern Macedonia. The contents of 20 elements-silver (Ag), aluminum (Al), arsenic (As), barium (Ba), calcium (Ca), cadmium (Cd), cobalt (Co), chromium (Cr), copper (Cu), iron (Fe), potassium (K), lithium (Li), magnesium (Mg), manganese (Mn), sodium (Na), nickel (Ni), Pb, strontium (Sr), vanadium (V), and (Zn) were determined by atomic emission spectrometry with inductively coupled plasma. Data processing was applied with combinations of multivariate statistical methods: factor analysis, principal component analysis, and cluster analysis. Moss' responsiveness to the atmospheric distribution of the selected elements was investigated in correlation to the specific geology of the region (soil dusting). Lithogenic distribution was characterized with the distribution of three dominant geochemical associations: F1: Al-Li-V-Cr-Ni-Co, F2: Ba-Ca-Sr, and F3: Cd-Zn-Pb-Cu. Spatial distribution was constructed for visualization of the factor deposition. Furthermore, air distribution (passive biomonitoring) versus soil geochemistry of the analyzed elements was examined. Significant correlations were singled out for Pb, Zn, and Cd and for Mg(moss)/Na(soil). Characteristic lithological anomaly characterized the presence of the oldest geological volcanic rocks. Zone 1 (Pb-Zn mine surrounding) presents a unique area with hydrothermal action of Pb-Zn mineralization leading to polymetallic enrichments in soil. This phenomenon strongly affects the environment, which is a natural geochemical imprint in this unique area (described with the strong dominance of the geochemical association Cd-Zn-Pb-Cu). PMID:26888226

  6. Pirquitasite, Ag2ZnSnS4

    PubMed Central

    Schumer, Benjamin N.; Downs, Robert T.; Domanik, Kenneth J.; Andrade, Marcelo B; Origlieri, Marcus J.

    2013-01-01

    Pirquitasite, ideally Ag2ZnSnS4 (disilver zinc tin tetra­sulfide), exhibits tetra­gonal symmetry and is a member of the stannite group that has the general formula A2BCX 4, with A = Ag, Cu; B = Zn, Cd, Fe, Cu, Hg; C = Sn, Ge, Sb, As; and X = S, Se. In this study, single-crystal X-ray diffraction data are used to determine the structure of pirquitasite from a twinned crystal from the type locality, the Pirquitas deposit, Jujuy Province, Argentina, with anisotropic displacement parameters for all atoms, and a measured composition of (Ag1.87Cu0.13)(Zn0.61Fe0.36Cd0.03)SnS4. One Ag atom is located on Wyckoff site Wyckoff 2a (symmetry -4..), the other Ag atom is statistically disordered with minor amounts of Cu and is located on 2c (-4..), the (Zn, Fe, Cd) site on 2d (-4..), Sn on 2b (-4..), and S on general site 8g. This is the first determination of the crystal structure of pirquitasite, and our data indicate that the space group of pirquitasite is I-4, rather than I-42m as previously suggested. The structure was refined under consideration of twinning by inversion [twin ratio of the components 0.91 (6):0.09 (6)]. PMID:23424398

  7. Interfacial Reactions and Joint Strengths of Sn- xZn Solders with Immersion Ag UBM

    NASA Astrophysics Data System (ADS)

    Jee, Y. K.; Yu, Jin

    2010-10-01

    The solder joint microstructures of immersion Ag with Sn- xZn ( x = 0 wt.%, 1 wt.%, 5 wt.%, and 9 wt.%) solders were analyzed and correlated with their drop impact reliability. Addition of 1 wt.% Zn to Sn did not change the interface microstructure and was only marginally effective. In comparison, the addition of 5 wt.% or 9 wt.% Zn formed layers of AgZn3/Ag5Zn8 at the solder joint interface, which increased drop reliability significantly. Under extensive aging, Ag-Zn intermetallic compounds (IMCs) transformed into Cu5Zn8 and Ag3Sn, and the drop impact resistance at the solder joints deteriorated up to a point. The beneficial role of Zn on immersion Ag pads was ascribed to the formation of Ag-Zn IMC layers, which were fairly resistant to the drop impact, and to the suppression of the brittle Cu6Sn5 phase at the joint interface.

  8. Effect of Ag doping and annealing on thermoelectric properties of PbTe

    SciTech Connect

    Bala, Manju Tripathi, T. S.; Avasthi, D. K.; Asokan, K.; Gupta, Srashti

    2015-06-24

    The present study reveals that annealing Ag doped PbTe thin films enhance thermoelectric properties. Phase formation was identified by using X-ray diffraction measurement. Annealing increases the crystallinity of both undoped and Ag doped PbTe. Electrical resistivity and thermoelectric power measurements are done using four probe and bridge method respectively. The increase in thermoelectric power of Ag doped PbTe is 29 % in comparison to undoped PbTe and it further increases to 34 % after annealing at 250{sup o} C for 1 hour whereas thermoelectric power increases by 14 % on annealing undoped PbTe thin films at same temperature.

  9. [Heavy metal contamination and Pb isotopic composition in natural soils around a Pb/Zn mining and smelting area].

    PubMed

    Sun, Rui; Shu, Fan; Hao, Wei; Li, Li; Sun, Wei-Ling

    2011-04-01

    The heavy metal (Pb, Zn, Cr, Cu, Cd, and Hg) concentrations in the A horizon and C horizon soils, collected around the Pb/Zn mining and smelting area of Shuikoushan in Hunan, China, were investigated, and the Pb isotopic compositions were also determined to identify the potential origin of Pb in the A horizon soil. Compared with C horizon soils, the A horizon soils exhibit elevated heavy metal concentrations, especially in the vicinity of the mining and smelting area. This reveals that the surface soil was contaminated to some degree. The contents of Pb, Zn, Cr, Cu, Cd, and Hg in soils are up to 3966.88, 2086.25, 135.31, 185.63, 56.15, and 16.434 mg/kg, respectively. The potential risks caused by different metals are in the order of Cd > Hg > Pb > Cu > Zn = Cr. Much higher potential ecological risk was observed for the central area (Shuikoushan Pb/Zn mining and smelting area) than for the surrounding area. About 34%, 33%, 11%, and 22% of the sampling sites demonstrate low, moderate, considerable, and very high potential ecological risk in the central area, while about 68%, 16%, 10%, and 6% of the sampling sites show low, moderate, considerable, and very high potential ecological risk in the surrounding area, respectively. Compared with the Pb isotopic compositions in the C horizon soils (206Pb/207Pb 1.168-1.246, 208 Pb/206 Pb 2.014-2.130), the Pb in the A horizon soils has lower 206 Pb/207Pb ratios (1.166-1.226) and higher 208Pb/206Pb ratios (2.043-2. 135). The Pb in the A horizon soils predominantly derives from two-component mixing resources. One is the parent materials of C horizon, and the other is the atmospheric deposition of the smelting flue gas dust.

  10. Effects of Oxide-Modified Spherical ZnO on Electrical Properties of Ag/ZnO Electrical Contact Material

    NASA Astrophysics Data System (ADS)

    Wei, Zhijun; Zhang, Lingjie; Shen, Tao; Qiao, Zhengyang; Yang, Hui; Fan, Xianping; Chen, Lawson

    2016-07-01

    Silver-zinc oxide (Ag/ZnO) electrical contact material is widely used as contacts of the medium duty switching devices. Effects of modified ZnO on properties of Ag/ZnO electrical contact material were investigated in this work. NiO and CuO were introduced to modify spherical ZnO by a chemical solution nano-coating method. Ag/ZnO contacts prepared using the modified spherical ZnO were produced by powder metallurgy (PM) method in a muffle furnace in temperature ranges from 750 to 900 °C. Results show that electrical conductivity, stability of relative density, and Vickers' hardness of Ag/ZnO electrical contact material can be improved by the addition of NiO because of the formation of NiO solid solution Zn0.2Ni0.8O. The addition of CuO to Ag/ZnO electrical contact material makes arcing energy and mass loss lower. Since this is attractive for a longer service life, using NiO and CuO co-modified ZnO as a second phase may be a promising way to improve properties of Ag/ZnO electrical contact material. Hence, the presented results could also be useful for the design of a new Ag/ZnO electrical contact material.

  11. Effects of Oxide-Modified Spherical ZnO on Electrical Properties of Ag/ZnO Electrical Contact Material

    NASA Astrophysics Data System (ADS)

    Wei, Zhijun; Zhang, Lingjie; Shen, Tao; Qiao, Zhengyang; Yang, Hui; Fan, Xianping; Chen, Lawson

    2016-09-01

    Silver-zinc oxide (Ag/ZnO) electrical contact material is widely used as contacts of the medium duty switching devices. Effects of modified ZnO on properties of Ag/ZnO electrical contact material were investigated in this work. NiO and CuO were introduced to modify spherical ZnO by a chemical solution nano-coating method. Ag/ZnO contacts prepared using the modified spherical ZnO were produced by powder metallurgy (PM) method in a muffle furnace in temperature ranges from 750 to 900 °C. Results show that electrical conductivity, stability of relative density, and Vickers' hardness of Ag/ZnO electrical contact material can be improved by the addition of NiO because of the formation of NiO solid solution Zn0.2Ni0.8O. The addition of CuO to Ag/ZnO electrical contact material makes arcing energy and mass loss lower. Since this is attractive for a longer service life, using NiO and CuO co-modified ZnO as a second phase may be a promising way to improve properties of Ag/ZnO electrical contact material. Hence, the presented results could also be useful for the design of a new Ag/ZnO electrical contact material.

  12. Ex situ synthesis and optical properties of ZnO-PbS nanocomposites

    NASA Astrophysics Data System (ADS)

    Ntwaeaborwa, O. M.; Kroon, R. E.; Kumar, V.; Dubroca, T.; Ahn, J.-P.; Park, J.-K.; Swart, H. C.

    2009-11-01

    Zinc oxide (ZnO) and lead sulphide (PbS) nanoparticles separately synthesized by a precipitation method were combined by an ex situ route to prepare ZnO-PbS nanocomposites with different molar ratios of ZnO and PbS. The structure and morphology of the ZnO, PbS and ZnO-PbS samples were analyzed with X-ray diffraction (XRD) and high-resolution transmission electron microscopy (HRTEM). A UV-vis spectrophotometer was used to collect the absorption and 325 nm He-Cd and 488 nm Ar lasers were used to collect the photoluminescence data from the samples. ZnO nanoparticles showed a broad and stable emission peak at ˜570 nm, while a strongly quantum confined emission from PbS nanoparticles was detected at ˜1344-1486 nm. The ZnO-PbS nanocomposites exhibited dual emission in the visible and near-infrared (NIR) regions that is associated with defects and recombination of excitonic centres in the ZnO and PbS nanoparticles, respectively. The PL intensity of the visible emission from the ZnO-PbS nanocomposite was shown to increase when the ZnO to PbS molar ratio was 5:1 and the emission was almost quenched at molar ratios of 1:1 and 1:5. For different molar ratios of ZnO to PbS, the PL intensity of the NIR emission from the ZnO-PbS nanocomposites was more intense than that of PbS nanoparticles.

  13. Pb and Zn accumulation in a Cd-hyperaccumulator (Viola baoshanensis).

    PubMed

    Wu, Chuan; Liao, Bin; Wang, Sheng-Long; Zhang, Jun; Li, Jin-Tian

    2010-08-01

    Viola baoshanensis has been identified as a Cd-hyperaccumulator, however, its ability to accumulate Pb or Zn is less certain. Therefore, this study focused on determining whether or not V. baoshanensis can accumulate Pb or Zn, by means of field survey, hydroponic and pot experiments. In addition, we also tried to obtain further information on the Cd hyperaccumulating characteristics of this species. Under field conditions, V. baoshanensis accumulated on average 1090 mg Cd kg(-1), 1902 mg Pb kg(-1) and 3428 mg Zn kg(-1) in its shoots, respectively. In hydroponic and pot experiments, V. baoshanensis showed high tolerance to Cd, Pb, and Zn, as well as the ability to accumulate exceptionally high concentrations of the three elements in its shoots (> 2% Cd, > 1% Pb, and > 0.5% Zn on a dry matter basis). These results, taken together, suggested that V. baoshanensis is not only a Cd-hyperaccumulator, but also a strong accumulator of Pb and Zn.

  14. Pb and Zn accumulation in a Cd-hyperaccumulator (Viola baoshanensis).

    PubMed

    Wu, Chuan; Liao, Bin; Wang, Sheng-Long; Zhang, Jun; Li, Jin-Tian

    2010-08-01

    Viola baoshanensis has been identified as a Cd-hyperaccumulator, however, its ability to accumulate Pb or Zn is less certain. Therefore, this study focused on determining whether or not V. baoshanensis can accumulate Pb or Zn, by means of field survey, hydroponic and pot experiments. In addition, we also tried to obtain further information on the Cd hyperaccumulating characteristics of this species. Under field conditions, V. baoshanensis accumulated on average 1090 mg Cd kg(-1), 1902 mg Pb kg(-1) and 3428 mg Zn kg(-1) in its shoots, respectively. In hydroponic and pot experiments, V. baoshanensis showed high tolerance to Cd, Pb, and Zn, as well as the ability to accumulate exceptionally high concentrations of the three elements in its shoots (> 2% Cd, > 1% Pb, and > 0.5% Zn on a dry matter basis). These results, taken together, suggested that V. baoshanensis is not only a Cd-hyperaccumulator, but also a strong accumulator of Pb and Zn. PMID:21166282

  15. Ag-doped ZnO nanorods synthesized by two-step method

    NASA Astrophysics Data System (ADS)

    Chen, Xian-Mei; Ji, Yong; Gao, Xiao-Yong; Zhao, Xian-Wei

    2012-11-01

    A two-step method is adopted to synthesize Ag-doped ZnO nanorods. A ZnO seed layer is first prepared on a glass substrate by thermal decomposition of zinc acetate. Ag-doped ZnO nanorods are then assembled on the ZnO seed layer using the hydrothermal method. The influences of the molar percentage of Ag ions to Zn ions (RAg/Zn) on the structural and optical properties of the ZnO nanorods obtained are carefully studied using X-ray diffractometry, scanning electron microscopy and spectrophotometry. Results indicate that Ag ions enter into the crystal lattice through the substitution of Zn ions. The (002) c-axis-preferred orientation of the ZnO nanorods decreases as RAg/Zn increases. At RAg/Zn > 1.0%, ZnO nanorods lose their c-axis-preferred orientation and generate Ag precipitates from the ZnO crystal lattice. The average transmissivity in the visible region first increases and then decreases as RAg/Zn increases. The absorption edge is first blue shifted and then red shifted. The influence of Ag doping on the average head face, and axial dimensions of the ZnO nanorods may be optimized to improve the average transmissivity at RAg/Zn < 1.0%.

  16. Synthesis, characterization and thermochemistry of synthetic Pb-As, Pb-Cu and Pb-Zn jarosites

    NASA Astrophysics Data System (ADS)

    Forray, Ferenc Lázár; Smith, A. M. L.; Navrotsky, A.; Wright, K.; Hudson-Edwards, K. A.; Dubbin, W. E.

    2014-02-01

    The enthalpy of formation from the elements of well characterized Pb-As, Pb-Cu, and Pb-Zn synthetic jarosites, corresponding to chemical formulas (H3O)0.68±0.03Pb0.32±0.002Fe2.86±0.14(SO4)1.69±0.08(AsO4)0.31±0.02(OH)5.59±0.28(H2O)0.41±0.02, (H3O)0.67±0.03Pb0.33±0.02Fe2.71±0.14Cu0.25±0.01(SO4)2±0.00(OH)5.96±0.30(H2O)0.04±0.002 and (H3O)0.57±0.03Pb0.43±0.02Fe2.70±0.14Zn0.21±0.01(SO4)2±0.00(OH)5.95±0.30(H2O)0.05±0.002, was measured by high temperature oxide melt solution calorimetry and gave ΔH°f = -3691.2 ± 8.6 kJ/mol, ΔH°f = -3653.6 ± 8.2 kJ/mol, and ΔH°f = -3669.4 ± 8.4 kJ/mol, respectively. Using estimated entropies, the standard Gibbs free energy of formation from elements at 298 K ΔG°f of the three compounds were calculated to be -3164.8 ± 9.1, -3131.4 ± 8.7, and -3153.6 ± 8.9 kJ/mol, respectively. Based on these free energies, their log Ksp values are -13.94 ± 1.89, -4.38 ± 1.81 and -3.75 ± 1.80, respectively. For this compounds, a log10{Pb2+}-pH diagram is presented. The diagram shows that the formation of Pb-As jarosite may decrease aqueous arsenic and lead concentrations to meet drinking water standards. The new thermodynamic data confirm that transformation of Pb-As jarosite to plumbojarosite is thermodynamically possible.

  17. Laser irradiation of ZnO:Al/Ag/ZnO:Al multilayers for electrical isolation in thin film photovoltaics

    NASA Astrophysics Data System (ADS)

    Crupi, Isodiana; Boscarino, Stefano; Torrisi, Giacomo; Scapellato, Giorgia; Mirabella, Salvatore; Piccitto, Giovanni; Simone, Francesca; Terrasi, Antonio

    2013-09-01

    Laser irradiation of ZnO:Al/Ag/ZnO:Al transparent contacts is investigated for segmentation purposes. The quality of the irradiated areas has been experimentally evaluated by separation resistance measurements, and the results are complemented with a thermal model used for numerical simulations of the laser process. The presence of the Ag interlayer plays two key effects on the laser scribing process by increasing the maximum temperature reached in the structure and accelerating the cool down process. These evidences can promote the use of ultra-thin ZnO:Al/Ag/ZnO:Al electrode in large-area products, such as for solar modules.

  18. Laser irradiation of ZnO:Al/Ag/ZnO:Al multilayers for electrical isolation in thin film photovoltaics

    PubMed Central

    2013-01-01

    Laser irradiation of ZnO:Al/Ag/ZnO:Al transparent contacts is investigated for segmentation purposes. The quality of the irradiated areas has been experimentally evaluated by separation resistance measurements, and the results are complemented with a thermal model used for numerical simulations of the laser process. The presence of the Ag interlayer plays two key effects on the laser scribing process by increasing the maximum temperature reached in the structure and accelerating the cool down process. These evidences can promote the use of ultra-thin ZnO:Al/Ag/ZnO:Al electrode in large-area products, such as for solar modules. PMID:24053228

  19. Ternary eutectic growth of nanostructured thermoelectric Ag-Pb-Te materials

    SciTech Connect

    Wu, Hsin-jay; Chen, Sinn-wen; Foo, Wei-jian; Jeffrey Snyder, G.

    2012-07-09

    Nanostructured Ag-Pb-Te thermoelectric materials were fabricated by unidirectionally solidifying the ternary Ag-Pb-Te eutectic and near-eutectic alloys using the Bridgeman method. Specially, the Bridgman-grown eutectic alloy exhibited a partially aligned lamellar microstructure, which consisted of Ag{sub 5}Te{sub 3} and Te phases, with additional 200-600 nm size particles of PbTe. The self-assembled interfaces altered the thermal and electronic transport properties in the bulk Ag-Pb-Te eutectic alloy. Presumably due to phonon scattering from the nanoscale microstructure, a low thermal conductivity ({kappa} = 0.3 W/mK) was achieved of the eutectic alloy, leading to a zT peak of 0.41 at 400 K.

  20. Synthesis, optical, photocatalytic, and electrochemical studies on Ag2S/ZnS and ZnS/Ag2S nanocomposites

    NASA Astrophysics Data System (ADS)

    Murugadoss, G.; Jayavel, R.; Rajesh Kumar, M.; Thangamuthu, R.

    2016-04-01

    Novel Ag2S/ZnS and ZnS/Ag2S nanocomposites were synthesized by a simple chemical method in air. Different morphologies were obtained for Ag2S/ZnS nanocomposites annealed at different temperatures. The products were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), UV-visible absorption, and photoluminescence (PL) spectroscopy. Thermal stability and phase transition of the sample were studied by TG-DTA. Compared the PL spectra of Ag2S/ZnS at 640 nm, it was significantly red shifted from 640 to 670 nm for reversed ZnS/Ag2S nanocomposites. The band gaps of nanocomposites were lying between 2.25 and 2.55 eV range. It has been found that as-synthesized powder has excellent photocatalytic activity toward degradation of methylene blue (MB) under visible light and electrochemical activity, indicating that Ag2S/ZnS and ZnS/Ag2S nanocomposites can play an important role as semiconductor photocatalyst and energy storage applications.

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

    NASA Astrophysics Data System (ADS)

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

    2013-04-01

    Soil-plant transfer of heavy metals in Pb-Zn mining sites from Alcudia Valley (South Spain). Authors: Miguel A. López-Berdonces¹; Pablo Higueras¹; Jose María Esbrí¹; Beatriz González-Corrochano¹; Eva Mª García- Noguero¹; Alba Martínez Coronado¹; Sergio Fernández-Calderón¹; Carolina García-Noguero¹ ¹Instituto de Geología Aplicada, Universidad Castilla la Mancha, Pza. Manuel Meca, 1. 13400 Almadén, Spain. Alcudia Valley is a vast territory recently declared Natural Park, located in South of Spain. It is an area rich in mineral deposits of Zn and Pb and mining exists since the first millennium BC., having its highest ore production between mid-nineteenth century and the middle of the twentieth. This area has been selected because has more than 120 abandoned mines without remediation actions, with dumps and tailings with high contents of zinc and lead sulfides, and Cu, Ag, Cd, As, Sb in minor concentrations. In this study we determinate the transfer rate of these metals from soils to plants represented by oak leaves (Quercus ilex), because this specie is common within the selected area. To evaluate the soil-plant transfer were studied the correlation of contents, total and extractable, in soil-leaves. Extractable fraction was done by for different methods in water, EPA 1312 sulfuric acid: nitric acid 60:40 v., Ammonium Acetate and EDTA. To establish the correlation between heavy metals from soils to plants is necessary to know the contents of these and bioavailable content in soil. Three areas (S. Quintín, Romanilla, Bombita) were selected, taking 24 samples of soils and leaves. Analyzed leaves by XRF showed that Mn, Pb, Zn and Mo in S.Quintin and Romanilla, Mn, Pb in Bombita, exceeded the toxicity threshold. The same samples analyzed by ICP show us the toxicity threshold is exceeded Pb, Zn and Hg in S.Quintin, and Pb in Romanilla. The heavy metal content in leaves compared between two techniques analytical gives an acceptable correlation Zn - Pb

  2. Influence of Ag thickness on structural, optical, and electrical properties of ZnS/Ag/ZnS multilayers prepared by ion beam assisted deposition

    SciTech Connect

    Leng Jian; Yu Zhinong; Xue Wei; Zhang Ting; Jiang Yurong; Zhang Jie; Zhang Dongpu

    2010-10-15

    The structural, optical, and electrical characteristics of zinc sulfide (ZnS)/Ag/ZnS (ZAZ) multilayer films prepared by ion beam assisted deposition on k9 glass have been investigated as a function of Ag layer thickness. The characteristics of ZAZ multilayer are significantly improved up insertion of optimal Ag thickness between ZnS layers. The results show that due to bombardment of Ar ion beam, distinct Ag islands evolve into continuous Ag films at a thin Ag thickness of about 4 nm. The thinner Ag film as a thickness of 2 nm leads to high sheet resistance and low transmittance for the interface scattering induced by the Ag islands or noncontinuous films; and when the Ag thickness is over 4 nm, the ZAZ multilayer exhibits a remarkably reduced sheet resistance between 7-80 {Omega}/sq for the increase in carrier concentration and mobility of Ag layer, and a high transmittance over 90% for the interference phenomena of multilayers and low absorption and surface scattering of Ag layer. The ZAZ multilayer with 14 nm Ag film has a figure of merit up to 6.32x10{sup -2} {Omega}{sup -1}, an average transmittance over 92% and a sheet resistance of 7.1 {Omega}/sq. The results suggest that ZAZ film has better optoelectrical properties than conditional indium tin oxide single layer.

  3. Defects responsible for abnormal n-type conductivity in Ag-excess doped PbTe thermoelectrics

    SciTech Connect

    Ryu, Byungki Lee, Jae Ki; Lee, Ji Eun; Joo, Sung-Jae; Kim, Bong-Seo; Min, Bok-Ki; Lee, Hee-Woong; Park, Su-Dong; Oh, Min-Wook

    2015-07-07

    Density functional calculations have been performed to investigate the role of Ag defects in PbTe thermoelectric materials. Ag-defects can be either donor, acceptor, or isovalent neutral defect. When Ag is heavily doped in PbTe, the neutral (Ag-Ag) dimer defect at Pb-site is formed and the environment changes to the Pb-rich/Te-poor condition. Under Pb-rich condition, the ionized Ag-interstitial defect (Ag{sub I}{sup +}) becomes the major donor. The formation energy of Ag{sub I}{sup +} is smaller than other native and Ag-related defects. Also it is found that Ag{sub I}{sup +} is an effective dopant. There is no additional impurity state near the band gap and the conduction band minimum. The charge state of Ag{sub I}{sup +} defect is maintained even when the Fermi level is located above the conduction band minimum. The diffusion constant of Ag{sub I}{sup +} is calculated based on the temperature dependent Fermi level, formation energy, and migration energy. When T > 550 K, the diffusion length of Ag within a few minutes is comparable to the grain size of the polycrystalline PbTe, implying that Ag is dissolved into PbTe and this donor defect is distributed over the whole lattice in Ag-excess doped polycrystalline PbTe. The predicted solubility of Ag{sub I}{sup +} well explains the increased electron carrier concentration and electrical conductivity reported in Ag-excess doped polycrystalline PbTe at T = 450–750 K [Pei et al., Adv. Energy Mater. 1, 291 (2011)]. In addition, we suggest that this abnormal doping behavior is also found for Au-doped PbTe.

  4. [Stabilization Treatment of Pb and Zn in Contaminated Soils and Mechanism Studies].

    PubMed

    Xie, Wei-qiang; Li, Xiao-mingi; Chen, Can; Chen, Xun-feng; Zhong, Yu; Zhong, Zhen-yu; Wan, Yong; Wang, Yan

    2015-12-01

    In the present work, the combined application of potassium dihydrogen phosphate, quick lime and potassium chloride was used to immobilize the Pb and Zn in contaminated soils. The efficiency of the process was evaluated through leaching tests and Tessier sequential extraction procedure. The mechanism of stabilization was analyzed by X-ray diffraction (XRD) and scanning electron microscope (SEM) to reveal the mechanism of stabilization. The results showed that the stabilizing efficiency of Pb contaminated soils was above 80% and the leaching concentrations of Pb, Zn were far below the threshold when the ratio of exogenous P and soil (mol · mol⁻¹) was 2:1-4: 1, the dosing ratio of CaO was 0.1%-0.5% ( mass fraction) and the dosage of potassium chloride was 0.02-0. 04 mol. Meanwhile, Pb and Zn in soil were transformed from the exchangeable fraction into residual fraction, which implied that the migration of Pb, Zn in soil could be confined by the stabilization treatment. XRD and SEM analysis revealed that Ca-P-Pb precipitation, lead orthophosphate [PbHP0₄, Pb₃ (PO₄)₂], pyromorphite (Pb-PO₄-Cl/OH) and mixed heavy metal deposits (Fe-PO₄- Ca-Pb-Zn-OH) could be formed after solidification/stabilization in which Pb and Zn could be wrapped up to form a solidified composition and to prevent leaching. PMID:27012000

  5. Formation of nanodots and enhancement of thermoelectric power induced by ion irradiation in PbTe:Ag composite thin films

    NASA Astrophysics Data System (ADS)

    Bala, Manju; Meena, Ramcharan; Gupta, Srashti; Pannu, Compesh; Tripathi, Tripurari S.; Varma, Shikha; Tripathi, Surya K.; Asokan, K.; Avasthi, Devesh K.

    2016-07-01

    Present study demonstrates an enhancement in thermoelectric power of 10% Ag doped PbTe (PbTe:Ag) thin films when irradiated with 200 keV Ar ion. X-ray diffraction showed an increase in crystallinity for both PbTe and PbTe:10Ag nano-composite films after Ar ion irradiation due to annealing of defects in the grain boundaries. The preferential sputtering of Pb and Te ions in comparison to Ag ions resulted in the formation of nano-dots. This was further confirmed by X-ray photoelectron spectroscopy (XPS). Such an enhancement in thermoelectric power of irradiated PbTe:10Ag films in comparison to pristine PbTe:10Ag film is attributed to the decrease in charge carrier concentration that takes part in the transport process via restricting the tunneling of carriers through the wider potential barrier formed at the interface of nano-dots.

  6. Properties of a new type Al/Pb-0.3%Ag alloy composite anode for zinc electrowinning

    NASA Astrophysics Data System (ADS)

    Yang, Hai-tao; Liu, Huan-rong; Zhang, Yong-chun; Chen, Bu-ming; Guo, Zhong-cheng; Xu, Rui-dong

    2013-10-01

    An Al/Pb-0.3%Ag alloy composite anode was produced via composite casting. Its electrocatalytic activity for the oxygen evolution reaction and corrosion resistance was evaluated by anodic polarization curves and accelerated corrosion test, respectively. The microscopic morphologies of the anode section and anodic oxidation layer during accelerated corrosion test were obtained by scanning electron microscopy. It is found that the composite anode (hard anodizing) displays a more compact interfacial combination and a better adhesive strength than plating tin. Compared with industrial Pb-0.3%Ag anodes, the oxygen evolution overpotentials of Al/Pb-0.3%Ag alloy (hard anodizing) and Al/Pb-0.3%Ag alloy (plating tin) at 500 A·m-2 were lower by 57 and 14 mV, respectively. Furthermore, the corrosion rates of Pb-0.3%Ag alloy, Al/Pb-0.3%Ag alloy (hard anodizing), and Al/Pb-0.3%Ag alloy (plating tin) were 13.977, 9.487, and 11.824 g·m-2·h-1, respectively, in accelerated corrosion test for 8 h at 2000 A·m-2. The anodic oxidation layer of Al/Pb-0.3%Ag alloy (hard anodizing) is more compact than Pb-0.3%Ag alloy and Al/Pb-0.3%Ag alloy (plating tin) after the test.

  7. Ordered surface alloy formation of immiscible metals: The case of Pb deposited on Ag(111)

    SciTech Connect

    Dalmas, J.; Oughaddou, H.; Leandri, C.; Gay, J-M.; Le Lay, G.; Treglia, G.; Aufray, B.; Bunk, O.

    2005-10-15

    The deposition of 1/3 Pb monolayer at room temperature onto Ag(111) leads to a ({radical}(3)x{radical}(3))R30 deg. superstructure. We present here a detailed structural study of this surface structure by synchrotron radiation surface x ray diffraction (SR-SXRD) and scanning tunnel microscopy (STM). We show that Pb atoms are embedded into the silver top surface layer forming an ordered Ag{sub 2}Pb surface alloy despite the strong tendency of the system to phase separate in the bulk. Quenched molecular dynamics simulations allow us to interpret this ordering reversal, in terms of size-mismatch induced surface alloying.

  8. Investigation of the potential for concealed base-metal mineralization at the Drenchwater Creek Zn-Pb-Ag occurrence, northern Alaska, using geology, reconnaissance geochemistry, and airborne electromagnetic geophysics

    USGS Publications Warehouse

    Graham, Garth E.; Deszcz-Pan, Maria; Abraham, Jared; Kelley, Karen D.

    2011-01-01

    No drilling has taken place at the Drenchwater occurrence, so alternative data sources (for example, geophysics) are especially important in assessing possible indicators of mineralization. Data from the 2005 electromagnetic survey define the geophysical character of the rocks at Drenchwater and, in combination with geological and surface-geochemical data, can aid in assessing the possible shallow (up to about 50 m), subsurface lateral extent of base-metal sulfide accumulations at Drenchwater. A distinct >3-km-long electromagnetic conductive zone (observed in apparent resistivity maps) coincides with, and extends further westward than, mineralized shale outcrops and soils anomalously high in Pb concentrations within the Kuna Formation; this conductive zone may indicate sulfide-rich rock. Models of electrical resistivity with depth, generated from inversion of electromagnetic data, which provide alongflight-line conductivity-depth profiles to between 25 and 50 m below ground surface, show that the shallow subsurface conductive zone occurs in areas of known mineralized outcrops and thins to the east. Broader, more conductive rock along the western ~1 km of the geophysical anomaly does not reach ground surface. These data suggest that the Drenchwater deposit is more extensive than previously thought. The application of inversion modeling also was applied to another smaller geochemical anomaly in the Twistem Creek area. The results are inconclusive, but they suggest that there may be a local conductive zone, possibly due to sulfides.

  9. Organic acids inhibit the formation of pyromorphite and Zn-phosphate in phosphorous amended Pb- and Zn-contaminated soil.

    PubMed

    Debela, F; Arocena, J M; Thring, R W; Whitcombe, T

    2013-02-15

    Pyromorphite (PY) and some zinc phosphates (Zn-P) are very sparingly soluble minerals and hence can immobilize Pb and Zn in contaminated soils. However, mechanisms leading to the poor efficiency of PY and Zn-P formation in contaminated soils amended with P still remain unclear. We studied the influence of two low molecular weight organic acids (LMWOA) - oxalic acid and citric acid and diethylene triamine pentaacetic acid (DTPA) - in PY and Zn-P formation in a P-amended contaminated soil. Despite the high levels of metals (∼4% Pb and 21% Zn) in the study soil, the addition of up to 1% inorganic P transformed only up to 37% and 17% of the total Pb and Zn to PY and Zn-P, respectively. Semi-quantitative estimates from a linear combination fitting of X-ray absorption near edge spectra (LC-XANES fitting) showed that the formation of PY decreased from 37% to 3% of the total Pb in the presence of oxalic acid and the addition of 1% P. The reduced PY formation may be associated with the increase in organic-bound Pb from 9% to 54% and decrease in carbonate associated Pb from 42% to 12% with oxalic acid addition as indicated by a chemical sequential extraction (SE) technique. Citric acid seemed to have a less adverse effect in PY formation than oxalic acid. Our data also suggests both oxalic and citric acids have less adverse effects on the efficiency of Zn-P formation. From this study we conclude that the abundance of LMWOA in soil environments can be one factor contributing to the poor efficiency of P amendments practices to effectively immobilize Pb and Zn in metal contaminated soils.

  10. Ag nanoparticle dispersed PbTiO3 percolative composite thin film with high permittivity

    NASA Astrophysics Data System (ADS)

    Wang, Zongrong; Hu, Tao; Tang, Liwen; Ma, Ning; Song, Chenlu; Han, Gaorong; Weng, Wenjian; Du, Piyi

    2008-12-01

    Ag nanoparticle dispersed PbTiO3 percolative composite thin films were prepared in situ by sol-gel method using Pb(NO3)2, Ti(C4H9O)4, and AgNO3 as raw materials and lactic acid along with citric acid as complexing agent. The size of the Ag nanoparticles measured by ultraviolet-visible spectra is about 3nm. The percolation effect occurs in composite thin films. The composite exhibits relatively high dielectric constant which is about five times higher than that of PbTiO3 thin film and comparatively low dielectric loss comparable to pure PbTiO3 system. It is highly attractive in application of high quality dielectric devices and miniaturization.

  11. Enhanced Raman scattering and nonlinear conductivity in Ag-doped hollow ZnO microspheres

    NASA Astrophysics Data System (ADS)

    Tringe, Joseph W.; Levie, Harold W.; McCall, Scott K.; Teslich, Nick E.; Wall, Mark A.; Orme, Christine A.; Matthews, Manyalibo J.

    2012-10-01

    Hollow spherical ZnO particles doped with Ag were synthesized with a two-step oxidation and sublimation furnace annealing process. Ag nanoparticle precipitates, as observed by transmission electron microscopy, were present in the polycrystalline ZnO matrix at Ag concentrations below 0.02 mol%, significantly below the 0.8 mol% solubility limit for Ag in ZnO. Enhanced Raman scattering of ZnO phonon modes is observed, increasing with Ag nanoparticle concentration. A further enhancement in Raman scattering due to resonance effects was observed for LO phonons excited by 2.33-eV photons as compared with Raman scattering under 1.96-eV excitation. Room-temperature photoluminescence spectra showed both a near-band-edge emission due to free exciton transitions and a mid-gap transition due to the presence of singly ionized oxygen vacancies. ZnO:Ag particles were measured electrically in a packed column and in monolithic form, and in both cases displayed nonlinear current-voltage characteristics similar to those previously observed in sintered ZnO:Ag monoliths where Ag-enhanced disorder at grain boundaries is thought to control current transport. We demonstrate therefore that Ag simultaneously modifies the electrical and optical properties of ZnO particles through the introduction of vacancies and other defects.

  12. Bioaccumulation of Zn and Ag Nanoparticles in the Earthworms (Eisenia fetida)

    NASA Astrophysics Data System (ADS)

    Ha, Lee Seung; Sung-Dae, Kim; Yi, Yang Song; Byeong-Gweon, Lee

    2014-05-01

    Many studies are carried out to evaluate environmental effects of engineered nanoparticles (ENPs). Most of the previous studies primarily focused on the effects of nanoparticles into the aquatic environment and human. Model studies predict that ENPs released into environment would transferred primarily to the soil of the terrestrial environment. Despite this prediction, biogeochemical behavior of ENPs in soil environment as well as bioavailability of ENPs to soil-dwelling organisms such as earthworm, springtail, isopod and nematodes are poorly understood. The main goal of this study was to compare the bioaccumulation factor (BAFs) and subcellular partitioning of nanoparticles in the soil-dwelling earthworm (Eisenia fetida) from ENP (ZnO and Ag nanoparticles) or ionic metal (Zn2+, Ag+) contaminated soil. And the sequential extraction was also used to determine the mobility of metals in soil which could be used as to predict bioavailability and compare that with bioaccumulation factor. The radiotracer method was employed to trace the transfer of ENPs and ionic metal among different environmental media and animals. Radiolabeled 65ZnO, 110mAgNPs coated with PVP or citrate were synthesized in the laboratory and their chemical and biological behavior was compared to ionic 65Zn and 110mAg. The BAFs of Zn and Ag in the earthworms were determined after animals exposed to the contaminated soils. After the 7 days of elimination phase, subcellular partitioning of metals were also obtained. BAF for ZnO(0.06) was 31 times lower than that for Zn ion (1.86), suggesting that ZnO was less bioavailable than its ionic form from contaminated soil. On the other hands, BAFs for AgNPs coated with PVP (0.12) or with citrate (0.11) were comparable to those for Ag ion (0.17), indicating that Ag from contaminated soil was bioavailable in a similar rate regardless of chemical forms. The subcellular partitioning results showed that bioaccumulated Zn from Zn ion and ZnO contaminated soil were

  13. Mobility and fractionation of Fe, Pb and Zn in river sediments from a silver and base-metals mining area: Taxco, México.

    PubMed

    Espinosa, E; Armienta, M A

    2007-08-01

    The impact of mining wastes on both the concentration and environmental mobility of Zn, Pb and Fe was studied in a shallow river. The studied tributary of the Taxco river is located south of the historical Ag, Zn, Cu and Pb mining area of Taxco, about 150 km south of México City. Methodology included total concentration determinations and sequential extraction analyses of the operational defined fractions of sediments. Results indicated that Fe, Pb and Zn concentrations are up to 5, 100 and 390 times respectively, greater than regional background concentrations. Higher contents of Pb and Zn were observed in the rainy season versus the dry season, whereas Fe was lower in the rainy season. Zinc and lead increased downflow in the dry season, and did not show any trend during the rainy season. Speciation showed that Zn was mainly linked to the carbonatic fraction (25-39%), to the hydrous Fe/Mn oxides fraction (15-25%) and to the organic matter and sulfide fraction (14-48%); lead was mainly associated to the hydrous Fe/Mn oxides (49-59%) and residual (22-39%) fractions; finally, iron was contained mainly in the residual (65-78%) and the hydrous Fe/Mn oxides fraction (15%). Mobility decreased according to the relation: Zn > Pb > Fe. Sediments were classified as strongly polluted in zinc, strongly to very strongly polluted in Pb, and moderately to strongly polluted in iron. However, a low proportion of metals in the exchangeable fractions, indicates low bioavailability. Limestone presence played a very important role on Zn and Pb fractionation and environmental mobility. Results show the importance of including geological background in river pollution studies.

  14. Modelling atmospheric bulk deposition of Pb, Zn and Cd near a former Pb-Zn mine in West Greenland using transplanted Flavocetraria nivalis lichens.

    PubMed

    Søndergaard, Jens; Bach, Lis; Asmund, Gert

    2013-03-01

    Atmospheric deposition of lead (Pb), zinc (Zn) and cadmium (Cd) was investigated near the former Black Angel Pb-Zn mine in Maarmorilik, West Greenland during 2010-2011. Thalli of the lichen Flavocetraria nivalis were transplanted from an uncontaminated site into sites near the mine and collected the following year. At 20 of the total 21 sites, concentrations of Pb, Zn and Cd were significantly elevated in lichens after 1 year of transplantation compared to initial concentrations. Elevated concentrations were observed within a distance of approx. 20 km from the mining area. Concentrations decreased with increasing distance from the mine and the relation was well described using a power function with a negative exponent (r(2)=0.90; 0.83 and 0.83 for Pb; Zn and Cd). To examine the relation between metal concentrations/uptake in lichen transplants and atmospheric bulk deposition, 10 Bergerhoff dust samplers were placed near lichen transplants and samplers and lichens were collected after a 7-weeks exposure period. A significant linear correlation was observed between metal concentrations in lichen transplants and atmospheric bulk metal deposition (r(2)=0.94; 0.88 and 0.89 for Pb; Zn and Cd). Combining the results and including an area distribution within a defined metal deposition area, the "annual" deposition of Pb, Zn and Cd as dust was estimated during the 2010-2011 snow-free period (∼5 months). The results reveal that 20 years after mine closure, 770 kg Pb, 3700 kg Zn and 24 kg Cd were still being deposited as dust per year (snow-free period only) within a distance of 20 km from the mine.

  15. Direct sunlight responsive Ag-ZnO heterostructure photocatalyst: Enhanced degradation of rhodamine B

    NASA Astrophysics Data System (ADS)

    Zhai, Hongju; Wang, Lijing; Sun, Dewu; Han, Donglai; Qi, Bing; Li, Xiuyan; Chang, Limin; Yang, Jinghai

    2015-03-01

    The catalytic activity of Ag-ZnO heterostructure on the photocatalytic degradation of rhodamine B was investigated. It demonstrated that Ag-ZnO heterostructure exhibited an enhanced photocatalytic activity compared to pure ZnO nanoparticles under direct sunlight. The possible factors to the photocatalytic acitivity of the sample were explored, including Ag content, dispersity and calcination temperature. It was shown that the sample dispersed by PVP, with 5% mol ratio Ag content, calcined at 400 °C showed the highest photocatalytic acitivity and this catalyst was reusable.

  16. The enhanced SERS effect of Ag/ZnO nanoparticles through surface hydrophobic modification

    NASA Astrophysics Data System (ADS)

    Li, Zhenjiang; Zhu, Kaixing; Zhao, Qian; Meng, Alan

    2016-07-01

    Ag/ZnO nanocomposites modified by a mixture of stearic acid (SA) and polyvinylpyrrolidone (PVP) were obtained using a heating reflux method. Fourier transform infrared spectroscopy (FT-IR) suggests that organic SA/PVP was bonded onto the surface of Ag/ZnO nanocrystals, converting the wettability property of the nanostructures from hydrophilic to hydrophobic. The modified Ag/ZnO nanostructures were confirmed as effective Raman substrates, with a 3-fold signal enhancement compared to the ordinary hydrophilic Ag/ZnO substrate for detecting Rh B molecules due to the hydrophobic condensation effect. It is expected that the modified Ag/ZnO nanoparticles have potential for SERS-based rapid detection of molecules.

  17. Facile Synthesis of Cadmium-Free Zn-In-S:Ag/ZnS Nanocrystals for Bio-Imaging

    PubMed Central

    Xuan, Tong-Tong; Liu, Jia-Qing; Yu, Cai-Yan; Xie, Rong-Jun; Li, Hui-Li

    2016-01-01

    High quality cadmium-free Zn-In-S:Ag doped-nanocrystals (d-NCs) were synthesized via a simple one-step noninjection route using silver nitrate, indium acetate, zinc acetate, oleylamine, S powder and 1-dodecanethiol as starting materials in an organic phase. The size and optical properties can be effectively tailored by controlling the reaction time, reaction temperature, Ag+ dopant concentration, and the molar ratio of In to Zn. The photoluminescence wavelength of as-prepared Zn-In-S:Ag NCs covered a broad visible range from 458 nm to 603 nm. After being passivated by protective ZnS shell, the photoluminescence quantum yield (PLQY) of Zn-In-S:Ag+ /ZnS was greatly improved to 43.5%. More importantly, the initial high PLQY of the obtained core/shell d-NCs in organic media can be preserved when being transferred into the aqueous media via ligand exchange. Finally, high quality Zn-In-S:Ag+ /ZnS d-NCs in aqueous phase were applied as bio-imaging agents for identifying living KB cells. PMID:27074820

  18. Facile Synthesis of Cadmium-Free Zn-In-S:Ag/ZnS Nanocrystals for Bio-Imaging.

    PubMed

    Xuan, Tong-Tong; Liu, Jia-Qing; Yu, Cai-Yan; Xie, Rong-Jun; Li, Hui-Li

    2016-01-01

    High quality cadmium-free Zn-In-S:Ag doped-nanocrystals (d-NCs) were synthesized via a simple one-step noninjection route using silver nitrate, indium acetate, zinc acetate, oleylamine, S powder and 1-dodecanethiol as starting materials in an organic phase. The size and optical properties can be effectively tailored by controlling the reaction time, reaction temperature, Ag(+) dopant concentration, and the molar ratio of In to Zn. The photoluminescence wavelength of as-prepared Zn-In-S:Ag NCs covered a broad visible range from 458 nm to 603 nm. After being passivated by protective ZnS shell, the photoluminescence quantum yield (PLQY) of Zn-In-S:Ag(+) /ZnS was greatly improved to 43.5%. More importantly, the initial high PLQY of the obtained core/shell d-NCs in organic media can be preserved when being transferred into the aqueous media via ligand exchange. Finally, high quality Zn-In-S:Ag(+) /ZnS d-NCs in aqueous phase were applied as bio-imaging agents for identifying living KB cells. PMID:27074820

  19. Facile Synthesis of Cadmium-Free Zn-In-S:Ag/ZnS Nanocrystals for Bio-Imaging

    NASA Astrophysics Data System (ADS)

    Xuan, Tong-Tong; Liu, Jia-Qing; Yu, Cai-Yan; Xie, Rong-Jun; Li, Hui-Li

    2016-04-01

    High quality cadmium-free Zn-In-S:Ag doped-nanocrystals (d-NCs) were synthesized via a simple one-step noninjection route using silver nitrate, indium acetate, zinc acetate, oleylamine, S powder and 1-dodecanethiol as starting materials in an organic phase. The size and optical properties can be effectively tailored by controlling the reaction time, reaction temperature, Ag+ dopant concentration, and the molar ratio of In to Zn. The photoluminescence wavelength of as-prepared Zn-In-S:Ag NCs covered a broad visible range from 458 nm to 603 nm. After being passivated by protective ZnS shell, the photoluminescence quantum yield (PLQY) of Zn-In-S:Ag+ /ZnS was greatly improved to 43.5%. More importantly, the initial high PLQY of the obtained core/shell d-NCs in organic media can be preserved when being transferred into the aqueous media via ligand exchange. Finally, high quality Zn-In-S:Ag+ /ZnS d-NCs in aqueous phase were applied as bio-imaging agents for identifying living KB cells.

  20. Sulfidation Roasting of Hemimorphite with Pyrite for the Enrichment of Zn and Pb

    NASA Astrophysics Data System (ADS)

    Min, Xiao-Bo; Xue, Ke; Ke, Yong; Zhou, Bo-Sheng; Li, Yang-Wen-Jun; Wang, Qing-Wei

    2016-06-01

    With the increasing consumption of zinc and the depletion of zinc sulfide ores, the exploitation of low-grade zinc oxide ores may be important for the sustainability of the zinc industry. Hemimorphite, a zinc hydroxyl silicate hydrate, is a significant source of Zn and Pb. It is difficult to obtain Zn and Pb from the hemimorphite using traditional technology. In this work, for the first time, sulfidation roasting of hemimorphite with pyrite was studied for the enrichment of Zn and Pb by a flotation process. Four stages of sulfidation roasting were determined based on x-ray diffraction and thermogravimetry analysis. Then, the effects of sulfidation temperature, pyrite dosage and reaction time on the sulfidation percentages were investigated at the laboratory scale. The experimental results showed that the sulfidation percentages of Pb and Zn were as high as 98.08% and 90.55% under optimum conditions, respectively. Finally, a flotation test was performed to enrich Zn and Pb in the sulfidation product. A flotation concentrate with 8.78% Zn and 9.25% Pb was obtained, and the recovery of Zn and Pb reached 56.14% and 75.94%, respectively.

  1. Sulfidation Roasting of Hemimorphite with Pyrite for the Enrichment of Zn and Pb

    NASA Astrophysics Data System (ADS)

    Min, Xiao-Bo; Xue, Ke; Ke, Yong; Zhou, Bo-Sheng; Li, Yang-Wen-Jun; Wang, Qing-Wei

    2016-09-01

    With the increasing consumption of zinc and the depletion of zinc sulfide ores, the exploitation of low-grade zinc oxide ores may be important for the sustainability of the zinc industry. Hemimorphite, a zinc hydroxyl silicate hydrate, is a significant source of Zn and Pb. It is difficult to obtain Zn and Pb from the hemimorphite using traditional technology. In this work, for the first time, sulfidation roasting of hemimorphite with pyrite was studied for the enrichment of Zn and Pb by a flotation process. Four stages of sulfidation roasting were determined based on x-ray diffraction and thermogravimetry analysis. Then, the effects of sulfidation temperature, pyrite dosage and reaction time on the sulfidation percentages were investigated at the laboratory scale. The experimental results showed that the sulfidation percentages of Pb and Zn were as high as 98.08% and 90.55% under optimum conditions, respectively. Finally, a flotation test was performed to enrich Zn and Pb in the sulfidation product. A flotation concentrate with 8.78% Zn and 9.25% Pb was obtained, and the recovery of Zn and Pb reached 56.14% and 75.94%, respectively.

  2. Efficient and stable CH3NH3PbI3-sensitized ZnO nanorod array solid-state solar cells.

    PubMed

    Bi, Dongqin; Boschloo, Gerrit; Schwarzmüller, Stefan; Yang, Lei; Johansson, Erik M J; Hagfeldt, Anders

    2013-12-01

    We report for the first time the use of a perovskite (CH3NH3PbI3) absorber in combination with ZnO nanorod arrays (NRAs) for solar cell applications. The perovskite material has a higher absorption coefficient than molecular dye sensitizers, gives better solar cell stability, and is therefore more suited as a sensitizer for ZnO NRAs. A solar cell efficiency of 5.0% was achieved under 1000 W m(-2) AM 1.5 G illumination for a solar cell with the structure: ZnO NRA/CH3NH3PbI3/spiro-MeOTAD/Ag. Moreover, the solar cell shows a good long-term stability. Using transient photocurrent and photovoltage measurements it was found that the electron transport time and lifetime vary with the ZnO nanorod length, a trend which is similar to that in dye-sensitized solar cells, DSCs, suggesting a similar charge transfer process in ZnO NRA/CH3NH3PbI3 solar cells as in conventional DSCs. Compared to CH3NH3PbI3/TiO2 solar cells, ZnO shows a lower performance due to more recombination losses.

  3. SrAgZn and EuAgZn with KHg{sub 2}-type structure—Structure, magnetic properties, and {sup 151}Eu Mössbauer spectroscopy

    SciTech Connect

    Gerke, Birgit; Rodewald, Ute Ch.; Niehaus, Oliver; Pöttgen, Rainer

    2013-07-15

    Samples of SrAgZn and EuAgZn were synthesized by reaction of the elements in sealed tantalum crucibles. Both structures were refined on the basis of single crystal X-ray diffractometer data: KHg{sub 2}-type, Imma, a=476.7(1), b=780.9(2), c=810.1(2) pm, R{sub 1}/wR{sub 2}=0.0189/0.0119, 381 F² values for SrAg{sub 1.12}Zn{sub 0.88} and a=474.43(9), b=760.8(2), c=799.0(2) pm, R{sub 1}/wR{sub 2}=0.0226/0.0483, 370 F² values for EuAg{sub 1.17}Zn{sub 0.83} with 13 variables per refinement. Silver and zinc are randomly distributed on the Hg position and build up three-dimensional networks. EuAgZn shows ferromagnetic ordering at 29(1) K. In the temperature range from 75 to 300 K the sample shows Curie–Weiss behaviour with μ{sub eff}=7.87(1) μ{sub B}/Eu atom and θ{sub P}=37.1(1) K, indicating divalent europium. {sup 151}Eu Mössbauer spectroscopic measurements confirmed the divalent state with an isomer shift of −9.31 mm/s at 78 K. Temperature dependent {sup 151}Eu data show first magnetic hyperfine field splitting at 25 K and a saturated magnetization of 17 T at 5.2 K. The temperature dependence can be described by an S=7/2 Brillouin function. - Graphical abstract: The near neighbor coordination of the strontium and europium atoms in SrAg{sub 1.12}Zn{sub 0.88}, EuAg{sub 1.17}Zn{sub 0.83}, and EuAuZn. - Highlights: • Synthesis of new intermetallic zinc compounds SrAgZn and EuAgZn. • Ferromagnetic ordering of EuAgZn at 29 K. • Magnetic hyperfine field splitting in the {sup 151}Eu Mössbauer spectrum.

  4. Plasmonic enhanced optical characteristics of Ag nanostructured ZnO thin films

    NASA Astrophysics Data System (ADS)

    Sarkar, Arijit; Gogurla, Narendar; Shivakiran Bhaktha, B. N.; Ray, Samit K.

    2016-04-01

    We have demonstrated the enhanced photoluminescence and photoconducting characteristics of plasmonic Ag–ZnO films due to the light scattering effect from Ag nanoislands. Ag nanoislands have been prepared on ITO-coated glass substrates by thermal evaporation followed by annealing. Plasmonic Ag–ZnO films have been fabricated by depositing ZnO over Ag nanoislands by sol–gel process. The band-edge emission of ZnO is enhanced for 170 nm sized Ag nanoislands in ZnO as compared to pure ZnO. The defect emission is also found to be quenched simultaneously for plasmonic Ag–ZnO films. The enhancement and quenching of photoluminescence at different wavelengths for Ag–ZnO films can be well understood from the localized surface plasmon resonance of Ag nanoislands. The Ag–ZnO M–S–M photoconductor device showed a tenfold increment in photocurrent and faster photoresponse as compared to the control ZnO device. The enhancement in photoresponse of the device is due to the increased photon absorption in ZnO films via scattering of the incident illumination.

  5. Hierarchical Ag/ZnO micro/nanostructure: Green synthesis and enhanced photocatalytic performance

    SciTech Connect

    Gao, Shuyan; Jia, Xiaoxia; Yang, Shuxia; Li, Zhengdao; Jiang, Kai

    2011-04-15

    Ag/ZnO metal-semiconductor nanocomposites with hierarchical micro/nanostructure have been prepared by the hydrothermal synthesis in the presence of bovine serum albumin (BSA). The results suggest that this biomolecule-assisted hydrothermal method is an efficient route for the fabrication of Ag/ZnO nanocomposites by using BSA both a shape controller and a reducing agent of Ag{sup +} ions. Moreover, Ag nanoparticles on the ZnO act as electron sinks, improving the separation of photogenerated electrons and holes, increasing the surface hydroxyl contents of ZnO, facilitating trapping the photoinduced electrons and holes to form more active hydroxyl radicals, and thus, enhancing the photocatalytic efficiency of ZnO. This is a good example for the organic combination of green chemistry and functional materials. -- Graphical Abstract: A green strategy is report to construct Ag/ZnO metal-semiconductor nanocomposites with hierarchical micro/nanostructure and enhanced photocatalytic activity. Display Omitted Research highlights: > Hierarchical micro/nanostructured Ag/ZnO nanocomposites have been prepared via a green route. > Ag nanoparticles improve the separation of photogenerated electrons and holes. > This facilitates trapping the photoinduced electrons and holes to form more hydroxyl radicals. Therefore, it enhances the photocatalytic efficiency of ZnO.

  6. Ag nanoparticle decorated nanoporous ZnO microrods and their enhanced photocatalytic activities.

    PubMed

    Deng, Quan; Duan, Xiaowei; Ng, Dickon H L; Tang, Haibin; Yang, Yong; Kong, Mingguang; Wu, Zhikun; Cai, Weiping; Wang, Guozhong

    2012-11-01

    Nanostructured Ag nanoparticles (Ag-NPs)/nanoporous ZnO micrometer-rods (n-ZnO MRs) have been synthesized by a two-step method. The n-ZnO MRs was initially prepared by solvothermal-assisted heat treatment. The rods had the diameter ranged from 90 to 150 nm and length between 0.5 and 3 μm. They were found to be porous and were composited of ZnO nanopartiles with size of about 20 nm. In the second stage, Ag-NPs with a diameter of 20-50 nm were anchored onto the surface of the as-prepared n-ZnO MRs by a photoreduction method. The Ag-NPs/n-ZnO MRs were evaluated for their ability to degrade methylene blue (MB) solution under visible to ultraviolet (UV) light irradiation. The rate of degradation of the as-prepared Ag-NPs/n-ZnO MRs was more than twice and nearly 5.6 times faster than that of using bare n-ZnO MRs under the UV and solar light irradiation, respectively. The formation of Schottky barriers in the regions between the Ag-NPs and n-ZnO MRs had improved the charge separation and consequently enhanced the efficiency of the degradation process. Moreover, the as-prepared hybrid structure exhibited high photostability, and 98% of degradation efficiency could be maintained even after being used five times. This endurance was attributed to the retardation of photocorrosion of ZnO as a result of the low concentration of surface defects in the as-prepared n-ZnO MRs. It also minimized the surface defects of the as-prepared n-ZnO MRs and consequently further inhibited the photocorrosion of ZnO when the deposited Ag-NPs were much more inclined to combine with the chemisorbed oxygen.

  7. Morphologically manipulated Ag/ZnO nanostructures as surface enhanced Raman scattering probes for explosives detection

    NASA Astrophysics Data System (ADS)

    Shaik, Ummar Pasha; Hamad, Syed; Ahamad Mohiddon, Md.; Soma, Venugopal Rao; Ghanashyam Krishna, M.

    2016-03-01

    The detection of secondary explosive molecules (e.g., ANTA, FOX-7, and CL-20) using Ag decorated ZnO nanostructures as surface enhanced Raman scattering (SERS) probes is demonstrated. ZnO nanostructures were grown on borosilicate glass substrates by rapid thermal oxidation of metallic Zn films at 500 °C. The oxide nanostructures, including nanosheets and nanowires, emerged over the surface of the Zn film leaving behind the metal residue. We demonstrate that SERS measurements with concentrations as low as 10 μM, of the three explosive molecules ANTA, FOX-7, and CL-20 over ZnO/Ag nanostructures, resulted in enhancement factors of ˜107, ˜107, and ˜104, respectively. These measurements validate the high sensitivity of detection of explosive molecules using Ag decorated ZnO nanostructures as SERS substrates. The Zn metal residue and conditions of annealing play an important role in determining the detection sensitivity.

  8. Accumulation of Cd, Pb and Zn by 19 wetland plant species in constructed wetland.

    PubMed

    Liu, Jianguo; Dong, Yuan; Xu, Hai; Wang, Deke; Xu, Jiakuan

    2007-08-25

    Uptake and distribution of Cd, Pb and Zn by 19 wetland plant species were investigated with experiments in small-scale plot constructed wetlands, into which artificial wastewater dosed with Cd, Pb and Zn at concentrations of 0.5, 2.0 and 5.0mgl(-1) was irrigated. The results showed that the removal efficiency of Cd, Pb and Zn from the wastewater were more than 90%. Generally, there were tens differences among the 19 plant species in the concentrations and quantity accumulations of the heavy metals in aboveground part, underground part and whole plants. The distribution ratios into aboveground parts for the metals absorbed by plants varied also largely from about 30% to about 90%. All the plants accumulated, in one harvest, 19.85% of Cd, 22.55% of Pb and 23.75% of Zn that were added into the wastewater. Four plant species, e.g. Alternanthera philoxeroides, Zizania latifolia, Echinochloa crus-galli and Polygonum hydropiper, accumulated high amounts of Cd, Pb and Zn. Monochoria vaginalis was capable for accumulating Cd and Pb, Isachne globosa for Cd and Zn, and Digitaria sanguinalis and Fimbristylis miliacea for Zn. The results indicated that the plants, in constructed wetland for the treatment of wastewater polluted by heavy metals, can play important roles for removal of heavy metals through phytoextraction. Selection of plant species for use in constructed wetland will influence considerably removal efficiency and the function duration of the wetland. PMID:17353090

  9. Accumulation of Cd, Pb and Zn by 19 wetland plant species in constructed wetland.

    PubMed

    Liu, Jianguo; Dong, Yuan; Xu, Hai; Wang, Deke; Xu, Jiakuan

    2007-08-25

    Uptake and distribution of Cd, Pb and Zn by 19 wetland plant species were investigated with experiments in small-scale plot constructed wetlands, into which artificial wastewater dosed with Cd, Pb and Zn at concentrations of 0.5, 2.0 and 5.0mgl(-1) was irrigated. The results showed that the removal efficiency of Cd, Pb and Zn from the wastewater were more than 90%. Generally, there were tens differences among the 19 plant species in the concentrations and quantity accumulations of the heavy metals in aboveground part, underground part and whole plants. The distribution ratios into aboveground parts for the metals absorbed by plants varied also largely from about 30% to about 90%. All the plants accumulated, in one harvest, 19.85% of Cd, 22.55% of Pb and 23.75% of Zn that were added into the wastewater. Four plant species, e.g. Alternanthera philoxeroides, Zizania latifolia, Echinochloa crus-galli and Polygonum hydropiper, accumulated high amounts of Cd, Pb and Zn. Monochoria vaginalis was capable for accumulating Cd and Pb, Isachne globosa for Cd and Zn, and Digitaria sanguinalis and Fimbristylis miliacea for Zn. The results indicated that the plants, in constructed wetland for the treatment of wastewater polluted by heavy metals, can play important roles for removal of heavy metals through phytoextraction. Selection of plant species for use in constructed wetland will influence considerably removal efficiency and the function duration of the wetland.

  10. Development of a ReaxFF potential for Ag/Zn/O and application to Ag deposition on ZnO

    NASA Astrophysics Data System (ADS)

    Lloyd, A.; Cornil, D.; van Duin, A. C. T.; van Duin, D.; Smith, R.; Kenny, S. D.; Cornil, J.; Beljonne, D.

    2016-03-01

    A new empirical potential has been derived to model an Ag-Zn-O system. Additional parameters have been included into the reactive force field (ReaxFF) parameter set established for ZnO to describe the interaction between Ag and ZnO for use in molecular dynamics (MD) simulations. The reactive force field parameters have been fitted to density functional theory (DFT) calculations performed on both bulk crystal and surface structures. ReaxFF accurately reproduces the equations of state determined for silver, silver zinc alloy and silver oxide crystals via DFT. It also compares well to DFT binding energies and works of separation for Ag on a ZnO surface. The potential was then used to model single point Ag deposition on polar (000 1 bar) and non-polar (10 1 bar0) orientations of a ZnO wurtzite substrate, at different energies. Simulation results then predict that maximum Ag adsorption on a ZnO surface requires deposition energies of ≤ 10 eV.

  11. Synthesis and characterization of highly-ordered ZnO/PbS core/shell heterostructures

    NASA Astrophysics Data System (ADS)

    Zhu, Y. F.; Zhou, G. H.; Ding, H. Y.; Liu, A. H.; Lin, Y. B.; Dong, Y. W.

    2011-11-01

    The strategy to manipulate nanoscale building blocks into well-organized heterostructures is very important to both material synthesis and nanodevice applications. In this work, highly-ordered ZnO/PbS core/shell nanowire arrays were fabricated by a facile and low temperature chemical route. Large area and well-aligned ZnO nanowire arrays were firstly fabricated on conductive glass substrates, and then the synthesis of ZnO/ZnS and ZnO/PbS core/shell nanowire arrays were realized by a chemical conversion method. The morphology, structure, and composition of the obtained nanostructures were confirmed by field-emission scanning electron microscopy, energy-dispersive X-ray analysis, and X-ray diffraction measurements. The optical properties of the synthesized nanostructures were investigated by micro-Raman and photoluminescence spectroscopy. In the synthesized ZnO/PbS core/shell nanowire arrays, the ZnO cores can provide direct conduction pathways for electron transport and PbS shells possess superior photoelectric performance. Therefore, the obtained ZnO/PbS core/shell nanostructures may have potential application in photovoltaic devices.

  12. Development of a new Pb-free solder: Sn-Ag-Cu

    SciTech Connect

    Miller, C.M.

    1995-02-10

    With the ever increasing awareness of the toxicity of Pb, significant pressure has been put on the electronics industry to get the Pb out of solder. This work pertains to the development and characterization of an alloy which is Pb-free, yet retains the proven positive qualities of current Sn-Pb solders while enhancing the shortcomings of Sn-Pb solder. The solder studied is the Sn-4.7Ag-1.7Cu wt% alloy. By utilizing a variety of experimental techniques the alloy was characterized. The alloy has a melting temperature of 217{degrees}C and exhibits eutectic melting behavior. The solder was examined by subjecting to different annealing schedules and examining the microstructural stability. The effect of cooling rate on the microstructure of the solder was also examined. Overall, this solder alloy shows great promise as a viable alternative to Pb-bearing solders and, as such, an application for a patent has been filed.

  13. Accumulation dynamics and cellular locations of Pb, Zn and Cd in resident and transplanted Flavocetraria nivalis lichens near a former Pb-Zn mine.

    PubMed

    Søndergaard, Jens

    2013-12-01

    Accumulation dynamics and cellular locations of lead (Pb), zinc (Zn) and cadmium (Cd) were studied in Flavocetraria nivalis lichens near the former Black Angel Pb-Zn Mine in West Greenland. Natural resident thalli were collected from four dust-contaminated sites near the mine. In addition, thalli were taken from an uncontaminated reference site and transplanted to the contaminated sites followed by a collection 1 year after. Total thalli metal contents were determined, and thalli were subjected to a sequential extraction procedure. After 1 year of transplantation, total Pb thalli contents were significantly elevated compared with initial concentrations at all sites (for Zn and Cd contents only at the two sites closest to the mine). However, transplanted thalli contained significantly less Pb (26 ± 12%), Zn (64 ± 13%) and Cd (34 ± 7 %) compared with resident thalli from these sites. Results from the sequential extraction procedure showed marked differences among Pb, Zn and Cd in the extracellular, intracellular and residual fraction. The lower total metal concentrations in transplanted compared with resident thalli at the contaminated sites were mostly due to a larger metal content bound in the residual fraction in resident thalli. In contrast, the metal content bound in the extracellular fraction were not significantly different in transplanted and resident thalli. The results indicate that extracellular-bound Pb, Zn and Cd in F. nivalis can be used as a proxy for recent (annual) atmospheric metal deposition whereas the large residual metal fraction in resident lichens indicate an accumulation of metal-containing particles in the thalli over time that includes several years of uptake.

  14. Label free detection of DNA on Au/ZnO/Ag hybrid structure based SERS substrate

    NASA Astrophysics Data System (ADS)

    Pal, Anil Kumar; Mohan, D. Bharathi

    2016-04-01

    Au/ZnO/Ag based SERS substrate was fabricated for the label free detection of DNA of Escherichia Coli bacteria. The SERS substrate was fabricated by growing ZnO nanorod arrays on thermally evaporated ultrathin Ag film of 5 nm thickness using hydrothermal process. Non-spherical like Au nanoparticles were decorated on ZnO nanorod arrays by sputtering technique with sputtering time of 45 sec. The surface of Au/ZnO/Ag was observed to be nearly superhydrophobic exhibiting the contact angle of 144 °. A low volume (5 µl) of aqueous solution of DNA of laboratory strain Escherichia Coli with very low concentration was adsorbed on fabricated SERS substrate by drop casting. The SERS detection of DNA molecules was achieved up to lower concentration of 10-8 M due to strong local electric field enhancement at the nanometer gap among Au nanoparticles and superhydrophobic nature of Au/ZnO/Ag surface.

  15. Probing the distribution and contamination levels of 10 trace metal/metalloids in soils near a Pb/Zn smelter in Middle China.

    PubMed

    Li, Zhonggen; Feng, Xinbin; Bi, Xiangyang; Li, Guanghui; Lin, Yan; Sun, Guangyi

    2014-03-01

    The horizontal and vertical distribution patterns and contamination status of ten trace metal/metalloids (Ag, Bi, Co, Cr, Ge, In, Ni, Sb, Sn, Tl) in soils around one of the largest Chinese Pb-Zn smelter in Zhuzhou City, Central China, were revealed. Different soil samples were collected from 11 areas, including ten agricultural areas and one city park area, with a total of 83 surface soil samples and six soil cores obtained. Trace metal/metalloids were determined by inductively coupled plasma-mass spectrometry after digestion by an acid mixture of HF and HNO3. The results showed that Ag, Bi, In, Sb, Sn, and Tl contents decreased both with the distance to the Pb-Zn smelter as well as the soil depth, hinting that these elements were mainly originated from the Pb-Zn smelting operations and were introduced into soils through atmospheric deposition. Soil Ge was influenced by the smelter at a less extent, while the distributions of Co, Cr, and Ni were roughly even among most sampling sites and soil depths, suggesting that they were primarily derived from natural sources. The contamination status, as revealed by the geo-accumulation index (I geo), indicated that In and Ag were the most enriched elements, followed by Sb, Bi, and Sn. In general, Cr, Tl, Co, Ni, and Ge were of an uncontaminated status.

  16. Effect of Ag and Pb Addition on Microstructural and Mechanical Properties of SAC 105 Solders

    NASA Astrophysics Data System (ADS)

    Molnar, Aliz; Janovszky, Dora; Kardos, Ibolya; Molnar, Istvan; Gacsi, Zoltan

    2015-10-01

    Melting and crystallization processes of lead-free and lead-contaminated alloys in near-equilibrium state were investigated. In addition, the effect of silver content up to 4 wt.% on the microstructure of Sn-Ag-Cu alloys was studied. The volume fraction of β-Sn decreased by half owing to 4 wt.% Ag content. Furthermore, contamination by lead strongly influences the properties of the solidified microstructure. The Pb grains appear as a result of two processes when the Pb content is equal to 0.5 wt.% or higher: Pb phase solidifies in the quaternary eutectic at 176°C, and Pb grains precipitate from the primary β-Sn solid solution grain during a solid state reaction. The freezing range enlarges to 51°C due to 2 wt.% Pb content owing to quaternary eutectic. Above 1 wt.% Pb content, the mechanical properties also improve due to grains of quaternary eutectic Pb and precipitated Pb grains with a size <1 μm.

  17. Increase of glutathione in mine population of Sedum alfredii: a Zn hyperaccumulator and Pb accumulator.

    PubMed

    Sun, Q; Ye, Z H; Wang, X R; Wong, M H

    2005-11-01

    Phytochelatins (PCs) have been induced in a large range of plant species, but their role in heavy metal tolerance is unclear. Sedum alfredii is a new zinc (Zn) hyperaccumulator and lead (Pb) accumulator found in an old Pb/Zn mine in the Zhejiang Province of China. Until now, the mechanisms of its hyperaccumulation/accumulation and tolerance were poorly understood. The aim of this work was to investigate whether PCs were differentially produced in mine populations of S. alfredii compared with a non-mine control of the same species. The results showed that plants from the mine site were more tolerant to increasing Zn and Pb concentrations than those from the control site. No PCs and cysteine (Cys) were detected by pre-column derivatization with HPLC fluorescence in any tissues of two populations at any treatment, which in turn indicated they were not responsible for Zn and Pb tolerance in the mine population. Instead, Zn and Pb treatments resulted in the increase of glutathione (GSH) for both populations in a tissue-dependent manner. Significant increases were observed in leaf, stem and root tissues of plants grown on the mine site. The results suggest that GSH, rather man PCs, may be involved in Zn and Pb transport, hyperaccumulation/accumulation and tolerance in mine population of S. alfredii. PMID:16225897

  18. Preparation, characterization and photocatalytic activity of visible-light-driven plasmonic Ag/AgBr/ZnFe{sub 2}O{sub 4} nanocomposites

    SciTech Connect

    Li, Xiaojuan Tang, Duanlian; Tang, Fan; Zhu, Yunyan; He, Changfa; Liu, Minghua Lin, Chunxiang; Liu, Yifan

    2014-08-15

    Highlights: • A plasmonic Ag/AgBr/ZnFe{sub 2}O{sub 4} photocatalyst has been successfully synthesized. • Ag/AgBr/ZnFe{sub 2}O{sub 4} nanocomposites exhibit high visible light photocatalytic activity. • Ag/AgBr/ZnFe{sub 2}O{sub 4} photocatalyst is stable and magnetically separable. - Abstract: A visible-light-driven plasmonic Ag/AgBr/ZnFe{sub 2}O{sub 4} nanocomposite has been successfully synthesized via a deposition–precipitation and photoreduction through a novel one-pot process. X-ray diffraction spectroscopy, X-ray photoelectron spectroscopy, scanning electron microscopy, transmission electron microscopy and UV–vis diffuse reflectance spectroscopy were employed to investigate the crystal structure, chemical composition, morphology, and optical properties of the as-prepared nanocomposites. The photocatalytic activities of the nanocomposites were evaluated by photodegradation of Rhodamine B (RhB) and phenol under visible light. The results demonstrated that the obtained Ag/AgBr/ZnFe{sub 2}O{sub 4} nanocomposites exhibited higher photocatalytic activity as compared to pure ZnFe{sub 2}O{sub 4}. In addition, the sample photoreduced for 20 min and calcined at 500 °C achieved the highest photocatalytic activity. Furthermore, the Ag/AgBr/ZnFe{sub 2}O{sub 4} nanocomposite has high stability under visible light irradiation and could be conveniently separated by using an external magnetic field.

  19. Removal, redistribution, and potential risks of soil Cd, Pb, and Zn after washing with various extractants.

    PubMed

    Chen, Chunle; Chen, Yanhui; Xie, Tuanhui; Wang, Ming Kuang; Wang, Guo

    2015-11-01

    The effectiveness of four different washing extractants--HCl, FeCl3, citric acid, and EDTA--in removing Cd, Pb, and Zn from polluted soil was studied. The removal of these metals, their redistribution between fractions, and the potential risks posed by them, in soils washed with the tested extractants, were examined. Although all the rounds of washing removed Cd, Pb, and Zn from soil, the first round removed more metals than subsequent rounds. Each of the four extractants had different effects on the removal of the metals. At the end of the first round of washing, HCl, EDTA, and FeCl3 were the most effective in removing Zn, Pb, and Cd, respectively. Both the single round and five successive rounds of washing with various extractants resulted in significant increases in Pb in the exchangeable/acid extractable fraction. Washing with HCl, EDTA, and FeCl3 significantly reduced potential risks (calculated as the Potential Risk Index, PRI) posed by Cd in washed soil. The first round of washing, using all extractants, increased the risks posed by Pb and Zn. However, five successive rounds of washing with FeCl3 and EDTA reduced the risk posed by Pb, and washing with citric acid and FeCl3 increased the risks posed by Zn. EDTA and HCl were better for reducing Zn risks, and successive washing with EDTA and FeCl3 were more effective in reducing Pb risks than the other extractants. Finally, five successive rounds of washing, with all the extractants, effectively reduced the potential risks posed by Cd. Among the four reagents, EDTA was advised to be the alternative of the washing reagent by significantly reducing the PRI values of Cd, Pb, and Zn.

  20. One pot synthesis of Ag nanoparticle modified ZnO microspheres in ethylene glycol medium and their enhanced photocatalytic performance

    SciTech Connect

    Tian Chungui; Li Wei; Pan Kai; Zhang Qi; Tian Guohui; Zhou Wei; Fu Honggang

    2010-11-15

    Ag nanoparticles (NPs) modified ZnO microspheres (Ag/ZnO microspheres) were prepared by a facile one pot strategy in ethylene glycol (EG) medium. The EG played two important roles in the synthesis: it could act as a reaction media for the formation of ZnO and reduce Ag{sup +} to Ag{sup 0}. A series of the characterizations indicated the successful combination of Ag NPs with ZnO microspheres. It was shown that Ag modification could greatly enhance the photocatalytic efficiency of ZnO microspheres by taking the photodegradation of Rhodamine B as a model reaction. With appropriate ratio of Ag and ZnO, Ag/ZnO microspheres showed the better photocatalytic performance than commercial Degussa P-25 TiO{sub 2}. Photoluminescence and surface photovoltage spectra demonstrated that Ag modification could effectively inhibit the recombination of the photoinduced electron and holes of ZnO. This is responsible for the higher photocatalytic activity of Ag/ZnO composites. -- Graphical abstract: A 'one-pot' strategy was developed for preparing the Ag/ZnO microspheres in ethylene glycol. The composites exhibited superior photocatalytic performance for photodegradation of Rhodamine B dye in water. Display Omitted

  1. Effects of Se and Zn supplementation on the antagonism against Pb and Cd in vegetables.

    PubMed

    He, P P; Lv, X Z; Wang, G Y

    2004-04-01

    The antagonistic effects of supplementation of Zn and Se to the soil on vegetables were studied in this work. In the pot experiment, Se (Se4+) and Zn (Zn2+) were applied, respectively, to the soil, in which the Chinese cabbage (Brassica rapa) and the lettuce (Lactuca sativa L.) were planted. As a result, Se and Zn were enriched evidently in the two vegetables. The contents of Pb and Cd in the two vegetables were decreased markedly while contents of some healthy mineral elements, like Mn and Mg, were increased to some extent when Se and Zn were applied. The antagonism of Se and Zn against Pb and Cd in plants was suggested. The farmland experiment on the lettuce was conducted to explore further the effect of supplementation of Zn and Se under the actual field conditions. Result came out to be that the enrichment of Zn and Se restrained the accumulation of Pb and Cd in the lettuce remarkably, as well as enhanced the absorption of some other nutritional elements, like Fe, Mn, Cu, Ca and Mg. Therefore, application of Se and Zn was proved to be an effective and feasible method to improve trace elements nutrition in the vegetables.

  2. Thermoelectric properties of p-type PbTe/Ag{sub 2}Te bulk composites by extrinsic phase mixing

    SciTech Connect

    Lee, Min Ho; Rhyee, Jong-Soo

    2015-12-15

    We investigated the thermoelectric properties of PbTe/Ag{sub 2}Te bulk composites, synthesized by hand milling, mixing, and hot press sintering. From x-ray diffraction and energy dispersive x-ray spectroscopy measurements, we observed Ag{sub 2}Te phase separation in the PbTe matrix without Ag atom diffusion. In comparison with previously reported pseudo-binary (PbTe){sub 1−x}(Ag{sub 2}Te){sub x} composites, synthesized by high temperature phase separation, the PbTe/Ag{sub 2}Te bulk composites fabricated with a low temperature phase mixing process give rise to p-type conduction of carriers with significantly decreased electrical conductivity. This indicates that Ag atom diffusion in the PbTe matrix changes the sign of the Seebeck coefficient to n-type and also increases the carrier concentration. Effective p-type doping with low temperature phase separation by mixing and hot press sintering can enhance the thermoelectric performance of PbTe/Ag{sub 2}Te bulk composites, which can be used as a p-type counterpart of n-type (PbTe){sub 1−x}(Ag{sub 2}Te){sub x} bulk composites.

  3. Simultaneous Incorporation of Cr, Zn, Cd, and Pb in the Goethite Structure

    SciTech Connect

    Kaur, Navdeep; Gräfe, Markus; Singh, Balwant; Kennedy, Brendan

    2009-10-21

    In order to improve our understanding of how the goethite crystal structure is affected by the incorporation of metals (and by variations in the amount of the incorporation), and to review any possible synergistic and antagonistic effects of co-metals, the present investigation focused on the incorporation of multiple (di-, tri-, and tetra-) metals, i.e. Cr, Zn, Cd, and Pb, in the goethite crystallographic structure. A series of single- and multi-metal M-Cr/Zn/Cd/Pb-substituted goethites with M/(M+Fe) molar ratios = 0.10 were prepared. The general sequence of metal entry in single-metal substituted goethites was Zn = Cr > Cd > Pb and in multi-metal-substituted goethites was Zn > Cr {ge} Cd > Pb. Simultaneous incorporation of Cr, Zn, Cd, and Pb up to 10.5 mole % was achieved in goethite. Synchrotron X-ray diffraction and extended X-ray absorption fine structure (EXAFS) techniques were employed to assess the structural characteristics of the synthesis products. Rietveld refinement of XRD data showed small changes in unit-cell parameters and Fe/M-Fe/M distances due to M substitution(s). A typical goethite-like crystalline structure remained intact, however. The unit-cell parameters were mutually, linearly correlated, though Fe/M-Fe/M distances were not, indicating that complex changes occurred at the local scale. In single-metal substituted goethites, incorporation of Cr reduced the unit-cell volume by 0.13% while that of Zn, Cd, and Pb increased it by 1.09, 3.58, and 0.56%, respectively. The changes in multi-metal-substituted goethites appeared to be the complex combination of that of the individually incorporated metals. The X-ray absorption near edge structure study of Pb-substituted goethites showed that the majority of associated Pb was Pb{sup 2+}, while Pb{sup 4+} was preferred over Pb{sup 2+} in the bulk structure. Measurements by EXAFS at the Fe K-edge indicated that the Fe polyhedra contracted in the presence of Cd{sup 2+} and Pb{sup 2+}, providing room for

  4. Band alignment of type I at (100)ZnTe/PbSe interface

    NASA Astrophysics Data System (ADS)

    Konovalov, Igor; Emelianov, Vitali; Linke, Ralf

    2016-06-01

    A junction of lattice-matched cubic semiconductors ZnTe and PbSe results in a band alignment of type I so that the narrow band gap of PbSe is completely within the wider band gap of ZnTe. The valence band offset of 0.27 eV was found, representing a minor barrier during injection of holes from PbSe into ZnTe. Simple linear extrapolation of the valence band edge results in a smaller calculated band offset, but a more elaborate square root approximation was used instead, which accounts for parabolic bands. PbSe was electrodeposited at room temperature with and without Cd2+ ions in the electrolyte. Although Cd adsorbs at the surface, the presence of Cd in the electrolyte does not influence the band offset.

  5. Incorporation of V, Zn and Pb into the crystalline phases of Portland clinker

    SciTech Connect

    Andrade, F.R.D.; Maringolo, V.; Kihara, Y

    2003-01-01

    Burning of industrial wastes in cement kilns has an increasing environmental importance, brought about by the incorporation of potentially hazardous elements into clinker crystalline phases and partial substitution of primary fuel and raw materials. In this study, experimental clinkers were synthesized, with the addition of V, Zn and Pb to a standard raw meal, from which a control clinker was obtained for comparison. The three metals were chosen as they are present in the alternative fuel petcoke (V) and in industrial wastes (Zn, Pb) commonly burned in cement kilns. Electron microprobe and scanning electron microscope analysis revealed the preferential partition of these metals among the clinker crystalline phases. It was observed that V has shown a preferential partition towards C{sub 2}S. Zn appears in higher amounts in periclase, and C{sub 3}S has higher Zn contents than C{sub 2}S. Pb concentrates in minute spherules and partitions toward C{sub 3}S in small amounts.

  6. Facile synthesis of pompon-like ZnO-Ag nanocomposites and their enhanced photocatalytic performance

    SciTech Connect

    Cheng, Yang; An, Liang; Lan, Jing; Gao, Fang; Tan, Ruiqin; Li, Xiao-min; Wang, Guang-hui

    2013-10-15

    Graphical abstract: - Highlights: • Pompon-like ZnO-Ag was prepared via heterothermal and photodeposition method. • Pompon-like ZnO-Ag is a excellent photocatalyst for degradation of azo dyes. • The photocatalytic and wetting properties were studied upon UV irradiation. • The discoloring efficiency of ZnO-Ag heterostructure toward to azo dyes is 99.1%. - Abstract: A series of pompon-like ZnO-Ag nanocomposites were prepared by hydrothermal method and photochemical deposition technique. Several characterizations indicated the successful deposition of Ag nanoparticles on ZnO. As a whole, the as-prepared composites present pompon-like nanostructures with a diameter of ∼10 μm. In detail, the nanostructural, chemical and optical properties were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), infrared spectroscopy (IR), ultra-visible spectra (UV). The photocatalytic degradation experiments under UV irradiation using Methyl Orange (MO) as a model dye were executed here. The relative results demonstrated that the pompon-like ZnO-Ag nanocomposite with a suitable content of Ag nanoparticles (about 4.82 wt%) has the highest photochemical activity, and the removal ratio of MO was 99.1% after 0.5 h adsorption and subsequent 2 h photodegradation processes. The excellent photocatalytic performance was attributed to the high surface areas of ZnO nanostructure and effectively separation of photo-generated charge on flower-like ZnO by employing Ag nanoparticles as a conductor.

  7. [Leaching behavior of Pb, Cd and Zn from soil stabilized by lime stabilized sludge].

    PubMed

    Li, Xiang; Song, Yun; Liu, Yong-Bing

    2014-05-01

    Stabilization of Pb, Cd and Zn spiked soil by using lime-stabilized sewage sludge( LSS) as amendment was investigated in this study, and the effectiveness was evaluated by using leaching tests ( TCLP, SPLP and de-ionized water) and modified BCR sequential extraction procedure. The results of TCLP indicated that the concentrations of heavy metals in TCLP leachate reduced significantly with the increase of the mass percentage of the LSS and the leaching reduction rates were as high as 99. 54% for Zn, 99. 60% for Pb, 99. 85% for Cd at 40% of LSS addition. When evaluated by SPLP and de-ionized water leaching method, the concentrations of Zn and Pb in leachate decreased obviously at 10% and 20% of LSS additions, but subsequently increased at 30% and 40% because of redissolution of Zn and Pb at strong base condition. After pH value of LLS-stabilized soil was adjusted by ferrous sulfate and phosphoric acid for recovering soil plantation function, the pH value of the soil decreased effectively, in the meantime promoting the stabilization effectiveness of Pb and Zn. The BCR test revealed that compared with the spiked soil exchangeable proportion of Zn, Pb, Cd in the soil and the soils adjusted by ferrous sulfate obviously declined, which implied the migration for Pb, Cd and Zn of contaminated soil could be confined. This study results show that municipal LSS can be reused in the stabilization of heavy metal contaminated soils and physical and chemical properties of LLS-stabilized soil are improved for plantation.

  8. Synthesis of spherical Ag/ZnO heterostructural composites with excellent photocatalytic activity under visible light and UV irradiation

    NASA Astrophysics Data System (ADS)

    Liu, Hairui; Hu, Yanchun; Zhang, Zhuxia; Liu, Xuguang; Jia, Husheng; Xu, Bingshe

    2015-11-01

    Ag nanoparticles (Ag-NPs) decorated ZnO microspheres (ZnO-MSs) heterostructural composites were fabricated via a two-step chemical method. The ZnO-MSs with the diameter about 700 nm was initially prepared by ultrasonic technology. Subsequently, Ag-NPs with a diameter of 20-50 nm were anchored onto the surface of the as-prepared ZnO-MSs by a microwave polyol process. The morphology, structural and optical properties of the as-synthesized materials were characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM) and high resolution TEM (HRTEM), X-ray photoelectron spectroscopy (XPS), UV-visible absorption spectroscopy, and photoluminescence spectroscopy. The results show that the surface plasmon absorption band of Ag/ZnO composites is distinctly broadened and the PL intensity of Ag/ZnO heterostructural composites varies with the increase of Ag loading. The photocatalytic activity of the Ag/ZnO composites were evaluated by the degradation of rhodamine B (RhB) solution under ultraviolet (UV) and visible light irradiation. The rate of degradation of the as-prepared Ag/ZnO composites was more than triple times faster than that of pure ZnO-MSs under UV light, which was ascribed to the formation of Schottky barriers in the regions between Ag-NPs and ZnO-MSs. Furthermore, Ag/ZnO composites exhibit superior photocatalytic activity over ZnO-MSs in the visible light region owing to the effective electron transfer from plasmon-excited Ag(0) nanoparticles to ZnO-MSs by strong localization of surface plasmon resonance (SPR). This can effectively decrease the recombination of electron-hole pairs, lead to a prolonged lifetime of the electron-holes pairs that promotes the degradation efficiency. The chemical stability and reusability of Ag/ZnO powders were also investigated.

  9. Research on Root Responses to Pb and Zn Combined Stress of Carex putuoshan.

    PubMed

    Hu, Yong-Lin; Tan, Jia-Lang; Wang, Cheng-Long; Yang, Zhan-Biao; Yang, Yuan-Xiang; Chen, Zhang; Lin, Li-Jin; Wang, Ying-Jun; Sun, Gang; Zhu, Xue-Mei; Shao, Ji-Rong; Zhou, Mei-Liang

    2016-01-01

    Pb hyper-accumulated Carex putuoshan was taken as experimental material and subjected to combined stress of Pb and Zn. The differential expression of proteins in their roots were analyzed by Proteomic Approach. The protein that was directly involved in the cellular defense under the Pb and Zn combined stress was separated, and expression of those genes was analyzed with Carex Evergold as control. The results were obtained by MALDI-TOF/MS analysis. After applying Pb and Zn combined stress, the expression of 9 protein spots (including 7 different proteins, 2 identical proteins, 1 unknown protein) in Carex putuoshan root was found to be significantly up-regulated. Five proteins were obtained from the 9 proteins related to carbohydrate metabolism, including malate dehydrogenase, glyceraldehyde-3-phosphate dehydrogenase, frutose-1,6-bisphosphate aldolase, enolase, and 6- phosphogluconate dehydrogenase. Two proteins were related to protein biosynthesis, including isoflavone reductase and phytochelatin synthase (PCS). From these proteins, the most important protein is PCS, which is a key enzyme in the synthesis of phytochelatins (PCs) and plays an important role in chelation. It is directly involved in cellular defense under Pb and Zn stress. After Pb and Zn combined stress, the CpPCS in Carex putuoshan was cloned. The full length of cDNA is 1461 bps, and it encodes 486 amino acids with molecular weight of 53.86 kD and pI value of 6.12. Two typical phytochelatin synthase subfamily domains constitute CpPCS protein, which includes three adjacent Cys-Cys elements in the C-terminal region. Phylogenetic analysis of PCS proteins from different species showed that it had the closest relationship with the Oryza sativa and Triticum aestivum. Real-time quantitative PCR analysis indicated that CpPCS and CePCS (Carex Evergold) genes were expressed in the root. The CpPCS and CePCS genes were up-regulated by Pb and Zn treatments. The expression of CpPCS was higher than that of Ce

  10. Research on Root Responses to Pb and Zn Combined Stress of Carex putuoshan.

    PubMed

    Hu, Yong-Lin; Tan, Jia-Lang; Wang, Cheng-Long; Yang, Zhan-Biao; Yang, Yuan-Xiang; Chen, Zhang; Lin, Li-Jin; Wang, Ying-Jun; Sun, Gang; Zhu, Xue-Mei; Shao, Ji-Rong; Zhou, Mei-Liang

    2016-01-01

    Pb hyper-accumulated Carex putuoshan was taken as experimental material and subjected to combined stress of Pb and Zn. The differential expression of proteins in their roots were analyzed by Proteomic Approach. The protein that was directly involved in the cellular defense under the Pb and Zn combined stress was separated, and expression of those genes was analyzed with Carex Evergold as control. The results were obtained by MALDI-TOF/MS analysis. After applying Pb and Zn combined stress, the expression of 9 protein spots (including 7 different proteins, 2 identical proteins, 1 unknown protein) in Carex putuoshan root was found to be significantly up-regulated. Five proteins were obtained from the 9 proteins related to carbohydrate metabolism, including malate dehydrogenase, glyceraldehyde-3-phosphate dehydrogenase, frutose-1,6-bisphosphate aldolase, enolase, and 6- phosphogluconate dehydrogenase. Two proteins were related to protein biosynthesis, including isoflavone reductase and phytochelatin synthase (PCS). From these proteins, the most important protein is PCS, which is a key enzyme in the synthesis of phytochelatins (PCs) and plays an important role in chelation. It is directly involved in cellular defense under Pb and Zn stress. After Pb and Zn combined stress, the CpPCS in Carex putuoshan was cloned. The full length of cDNA is 1461 bps, and it encodes 486 amino acids with molecular weight of 53.86 kD and pI value of 6.12. Two typical phytochelatin synthase subfamily domains constitute CpPCS protein, which includes three adjacent Cys-Cys elements in the C-terminal region. Phylogenetic analysis of PCS proteins from different species showed that it had the closest relationship with the Oryza sativa and Triticum aestivum. Real-time quantitative PCR analysis indicated that CpPCS and CePCS (Carex Evergold) genes were expressed in the root. The CpPCS and CePCS genes were up-regulated by Pb and Zn treatments. The expression of CpPCS was higher than that of Ce

  11. Role of Bound Zn(II) in the CadC Cd(II)/Pb(II)/Zn(II)-Responsive Repressor

    SciTech Connect

    Kandegedara, A.; Thiyagarajan, S; Kondapalli, K; Stemmler, T; Rosen, B

    2009-01-01

    The Staphylococcus aureus plasmid pI258 cadCA operon encodes a P-type ATPase, CadA, that confers resistance to Cd(II)/Pb(II)/Zn(II). Expression is regulated by CadC, a homodimeric repressor that dissociates from the cad operator/promoter upon binding of Cd(II), Pb(II), or Zn(II). CadC is a member of the ArsR/SmtB family of metalloregulatory proteins. The crystal structure of CadC shows two types of metal binding sites, termed Site 1 and Site 2, and the homodimer has two of each. Site 1 is the physiological inducer binding site. The two Site 2 metal binding sites are formed at the dimerization interface. Site 2 is not regulatory in CadC but is regulatory in the homologue SmtB. Here the role of each site was investigated by mutagenesis. Both sites bind either Cd(II) or Zn(II). However, Site 1 has higher affinity for Cd(II) over Zn(II), and Site 2 prefers Zn(II) over Cd(II). Site 2 is not required for either derepression or dimerization. The crystal structure of the wild type with bound Zn(II) and of a mutant lacking Site 2 was compared with the SmtB structure with and without bound Zn(II). We propose that an arginine residue allows for Zn(II) regulation in SmtB and, conversely, a glycine results in a lack of regulation by Zn(II) in CadC. We propose that a glycine residue was ancestral whether the repressor binds Zn(II) at a Site 2 like CadC or has no Site 2 like the paralogous ArsR and implies that acquisition of regulatory ability in SmtB was a more recent evolutionary event.

  12. Theoretical assessment of phosphate amendments for stabilization of (Pb+Zn) in polluted soil.

    PubMed

    Raicevic, S; Perovic, V; Zouboulis, A I

    2009-05-01

    Contamination of the environment with toxic metals, such as lead (Pb), represents a serious concern for human health. Most of the studies on Pb stabilization were performed using various phosphorus-containing amendments that can reduce Pb mobility and bioavailability by the sorption and precipitation of new, stable pyromorphite-type minerals, presenting very low solubility and bioaccessibility. However, the presence of competing ions, such as zinc (Zn), can reduce stabilization efficacy. The role of chemical composition on the stability of immobilization products of Pb and Zn by the addition of hydroxyapatite (HAP) or fluoroapatite (FAP) has been examined in this paper. In this analysis we used a theoretical criterion which is based on calculation of the ion-ion interaction potential, representing the main term of the cohesive energy of the matrix/pollutant system. It has been demonstrated that the stability of the HAP matrix decreases and that the stability of the FAP matrix increases with the Pb immobilization in the presence of Zn. The results of this analysis point out FAP as an advantageous amendment for the immobilization of Pb in the presence of Zn.

  13. SEMICONDUCTOR DEVICES: Ag/PEPC/NiPc/ZnO/Ag thin film capacitive and resistive humidity sensors

    NASA Astrophysics Data System (ADS)

    Karimov, Kh. S.; Yew Cheong, Kuan; Saleem, M.; Murtaza, Imran; Farooq, M.; Fauzi Mohd Noor, Ahmad

    2010-05-01

    A thin film of blended poly-N-epoxypropylcarbazole (PEPC) (25 wt.%), nickel phthalocyanine (NiPc) (50 wt.%) and ZnO nano-powder (25 wt.%) in benzene (5 wt.%) was spin-coated on a glass substrate with silver electrodes to produce a surface-type Ag/PEPC/NiPc/ZnO/Ag capacitive and resistive sensor. Sensors with two different PEPC/NiPc/ZnO film thicknesses (330 and 400 nm) were fabricated and compared. The effects of humidity on capacitance and resistance of the Ag/PEPC/NiPc/ZnO/Ag sensors were investigated at two frequencies of the applied voltage: 120 Hz and 1 kHz. It was observed that at 120 Hz under humidity of up to 95% RH the capacitance of the sensors increased by 540 times and resistance decreased by 450 times with respect to humidity conditions of 50% RH. It was found that the sensor with a thinner semiconducting film (330 nm) was more sensitive than the sensor with a thicker film (400 nm). The sensitivity was improved when the sensor was used at a lower frequency as compared with a high frequency. It is assumed that the humidity response of the sensors is associated with absorption of water vapors and doping of water molecules in the semiconductor blend layer. This had been proven by simulation of the capacitance-humidity relationship.

  14. ZnO/Ag composite nanorod arrays for surface-plasmon-enhanced emission study

    SciTech Connect

    Pal, Anil Kumar E-mail: d.bharathimohan@gmail.com; Mohan, D. Bharathi E-mail: d.bharathimohan@gmail.com

    2014-04-24

    The surface plasmon resonance enhanced emission through coupling of surface plasmons and exciton band energies is studied in hybrid ZnO/Ag nanostructure. The catalytic growth of ZnO nanorods is controlled in seed mediated growth by altering size distribution of Ag nanoislands. X-ray diffraction shows a predominant (002) crystal plane confirming the preferential growth of ZnO nanorods on as-deposited Ag. Increase of surface roughness in Ag film by post deposition annealing process enhances the light emission due to momentum matching between surface plasmons and excitons as well as a red shift of 32 meV occurs due to multi phonon and phonon-exciton interaction.

  15. Pb(core)/ZnO(shell) nanowires obtained by microwave-assisted method

    PubMed Central

    2011-01-01

    In this study, Pb-filled ZnO nanowires [Pb(core)/ZnO(shell)] were synthesized by a simple and novel one-step vapor transport and condensation method by microwave-assisted decomposition of zinc ferrite. The synthesis was performed using a conventional oven at 1000 W and 5 min of treatment. After synthesis, a spongy white cotton-like material was obtained in the condensation zone of the reaction system. HRTEM analysis revealed that product consists of a Pb-(core) with (fcc) cubic structure that preferentially grows in the [111] direction and a hexagonal wurtzite ZnO-(Shell) that grows in the [001] direction. Nanowire length was more than 5 μm and a statistical analysis determined that the shell and core diameters were 21.00 ± 3.00 and 4.00 ± 1.00 nm, respectively. Experimental, structural details, and synthesis mechanism are discussed in this study. PMID:21985637

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

    PubMed

    Kovács, Elza; Dubbin, William E; Tamás, János

    2006-05-01

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

  17. Temperature-dependent thermal expansion of cast and hot-pressed LAST (Pb-Sb-Ag-Te) thermoelectric materials

    SciTech Connect

    Ren, Fei; Hall, Bradley D.; Case, Eldon D; Timm, Edward J; Trejo, Rosa M; Meisner, Roberta Ann; Lara-Curzio, Edgar

    2009-01-01

    The thermal expansion for two compositions of cast and hot-pressed LAST (Pb Sb Ag Te) n-type thermoelectric materials has been measured between room temperature and 673K via thermomechanical analysis (TMA). In addition, using high-temperature X-ray diffraction (HT-XRD), the thermal expansion for both cast and hot-pressed LAST materials was determined from the temperature-dependent lattice parameters measured between room temperature and 623 K. The TMA and HT-XRD determined values of the coefficient of thermal expansion (CTE) for the LAST compositions ranged between 20106K1 and 24106K1, which is comparable to the CTE values for other thermoelectric materials including PbTe and Bi2Te3. The CTE of the LAST specimens with a higher Ag content (Ag0.86Pb19Sb1.0Te20) exhibited a higher CTE value than that of the LAST material with a lower Ag content (Ag0.43Pb18Sb1.2Te20). In addition, a peak in the temperature-dependent CTE was observed between room temperature and approximately 450K for both the cast and hot-pressed LAST with the Ag0.86Pb19Sb1.0Te20 composition, whereas the CTE of the Ag0.43Pb18Sb1.2Te20 specimen increased monotonically with temperature.

  18. Preparation, characterization, and photocatalytic performance of pear-shaped ZnO/Ag core-shell submicrospheres

    NASA Astrophysics Data System (ADS)

    Guo, Xiao-Hua; Ma, Jian-Qi; Ge, Hong-Guang

    2013-05-01

    Pear-shaped ZnO/Ag core-shell submicrospheres with good monodispersity were prepared via a seed-mediated particle growth procedure, where metal Ag (by reducing Ag+ with Sn2+) deposited on the as-prepared ZnO submicrospheres served as seeds (nucleation sites) for further growth of Ag nanoparticles. The as-prepared samples were characterized by X-ray diffraction, transmission electron microscopy, energy-dispersive X-ray spectroscopy, ultraviolet-visible and photoluminescence spectra. Structure characterization demonstrates that the ZnO/Ag composites are composed of pear-shaped wurtzite ZnO submicrosphere core and Ag nanoparticles (nanoshell). Photoluminescence indicates that Ag nanoshell can effectively inhibit the recombination of the photoinduced electrons and holes of ZnO. This is responsible for the higher photocatalytic activity of the ZnO/Ag core-shell composites. The photocatalytic performance of the prepared ZnO/Ag samples for degradation of Rhodamine B was evaluated with a comparative study. The relationship between the structure of the samples and their photocatalytic performance shows that Ag deposits can significantly enhance the photocatalytic efficiency of ZnO submicrospheres.

  19. Immobilization of Cu, Pb and Zn in mine-contaminated soils using reactive materials.

    PubMed

    Navarro, Andrés; Cardellach, Esteve; Corbella, Mercé

    2011-02-28

    Immobilization processes were used to chemically stabilize soil contaminated with Cu, Pb and Zn from mine tailings and industrial impoundments. We examined the effectiveness of ordinary Portland cement (OPC), phosphoric acid and MgO at immobilizing Cu, Pb and Zn in soil contaminated by either mine tailings or industrial and mine wastes. The effectiveness was evaluated using column leaching experiments and geochemical modelling, in which we assessed possible mechanisms for metal immobilization using PHREEQC and Medusa numerical codes. Experimental results showed that Cu was mobilized in all the experiments, whereas Pb immobilization with H(3)PO(4) may have been related to the precipitation of chloropyromorphite. Thus, the Pb concentrations of leachates of pure mining and industrial contaminated soils (32-410 μg/l and 430-1000 μg/l, respectively) were reduced to 1-60 and 3-360 μg/l, respectively, in the phosphoric acid experiment. The mobilization of Pb at high alkaline conditions, when Pb(OH)(4)(-) is the most stable species, may be the main obstacle to the use of OPC and MgO in the immobilization of this metal. In the mining- and industry-contaminated soil, Zn was retained by OPC but removed by MgO. The experiments with OPC showed the Zn decrease in the leachates of mining soil from 226-1960 μg/l to 92-121 μg/l. In the industrial contaminated soil, the Zn decrease in the leachates was most elevated, showing >2500 μg/l in the leachates of contaminated soil and 76-173 μg/l in the OPC experiment. Finally, when H(3)PO(4) was added, Zn was mobilized.

  20. Immobilization of Cu, Pb and Zn in mine-contaminated soils using reactive materials.

    PubMed

    Navarro, Andrés; Cardellach, Esteve; Corbella, Mercé

    2011-02-28

    Immobilization processes were used to chemically stabilize soil contaminated with Cu, Pb and Zn from mine tailings and industrial impoundments. We examined the effectiveness of ordinary Portland cement (OPC), phosphoric acid and MgO at immobilizing Cu, Pb and Zn in soil contaminated by either mine tailings or industrial and mine wastes. The effectiveness was evaluated using column leaching experiments and geochemical modelling, in which we assessed possible mechanisms for metal immobilization using PHREEQC and Medusa numerical codes. Experimental results showed that Cu was mobilized in all the experiments, whereas Pb immobilization with H(3)PO(4) may have been related to the precipitation of chloropyromorphite. Thus, the Pb concentrations of leachates of pure mining and industrial contaminated soils (32-410 μg/l and 430-1000 μg/l, respectively) were reduced to 1-60 and 3-360 μg/l, respectively, in the phosphoric acid experiment. The mobilization of Pb at high alkaline conditions, when Pb(OH)(4)(-) is the most stable species, may be the main obstacle to the use of OPC and MgO in the immobilization of this metal. In the mining- and industry-contaminated soil, Zn was retained by OPC but removed by MgO. The experiments with OPC showed the Zn decrease in the leachates of mining soil from 226-1960 μg/l to 92-121 μg/l. In the industrial contaminated soil, the Zn decrease in the leachates was most elevated, showing >2500 μg/l in the leachates of contaminated soil and 76-173 μg/l in the OPC experiment. Finally, when H(3)PO(4) was added, Zn was mobilized. PMID:21190796

  1. Abandoned PbZn mining wastes and their mobility as proxy to toxicity: A review.

    PubMed

    Gutiérrez, Mélida; Mickus, Kevin; Camacho, Lucy Mar

    2016-09-15

    Lead and zinc (PbZn) mines are a common occurrence worldwide; and while approximately 240 mines are active, the vast majority have been abandoned for decades. Abandoned mining wastes represent a serious environmental hazard, as Pb, Zn and associated metals are continuously released into the environment, threatening the health of humans and affecting ecosystems. Iron sulfide minerals, when present, can form acid mine drainage and increase the toxicity by mobilizing the metals into more bioavailable forms. Remediation of the metal waste is costly and, in the case of abandoned wastes, the responsible party(ies) for the cleanup can be difficult to determine, which makes remediation a complex and lengthy process. In this review, we provide a common ground from a wide variety of investigations about concentrations, chemical associations, and potential mobility of Pb, Zn and cadmium (Cd) near abandoned PbZn mines. Comparing mobility results is a challenging task, as instead of one standard methodology, there are 4-5 different methods reported. Results show that, as a general consensus, the metal content of soils and sediments vary roughly around 1000mg/kg for Zn, 100 for Pb and 10 for Cd, and mobilities of Cd>Zn>Pb. Also, mobility is a function of pH, particle size, and formation of secondary minerals. New and novel remediation techniques continue to be developed in laboratories but have seldom been applied to the field. Remediation at most of the sites has consisted of neutralization (e.g. lime,) for acid mine discharge, and leveling followed by phytostabilization. In the latter, amendments (e.g. biochar, fertilizers) are added to boost the efficiency of the treatment. Any remediation method has to be tested before being implemented as the best treatment is site-specific. Potential treatments are described and compared. PMID:27179321

  2. Synthesis of highly efficient antibacterial agent Ag doped ZnO nanorods: Structural, Raman and optical properties

    SciTech Connect

    Jan, Tariq; Iqbal, Javed; Ismail, Muhammad; Mahmood, Arshad

    2014-04-21

    Here, synthesis, structural, morphological, Raman, optical properties and antibacterial activity of undoped and Ag doped ZnO nanorods by chemical co-precipitation technique have been reported. Structural analysis has revealed that Ag doping cannot deteriorate the structure of ZnO and wurtzite phase is maintained. Lattice constants are found to be decreased with the Ag doping. Fourier transform infrared and Raman spectroscopy also confirm the X-ray diffraction results. Scanning electron microscopy results have demonstrated the formation of ZnO nanorods with average diameter and length of 96 nm and 700 nm, respectively. Raman spectroscopy results suggest that the Ag doping enhances the number of defects in ZnO crystal. It has been found from optical study that Ag doping results in positional shift of band edge absorption peak. This is attributed to the successful incorporation of Ag dopant into ZnO host matrix. The antibacterial activity of prepared nanorods has been determined by two different methods and compared to that of undoped ZnO nanorods. Ag doped ZnO nanorods exhibit excellent antibacterial activity as compared to that of undoped ZnO nanorods. This excellent antibacterial activity may be attributed to the presence of oxygen vacancies and Zn{sup 2+} interstitial defects. Our preliminary findings suggest that Ag doped ZnO nanorods can be used externally to control the spreading of infections related with tested bacterial strains.

  3. Concentrations of Cd, Pb, Mn and Zn in feathers and diet in heron chicks in Korea.

    PubMed

    Kim, Jungsoo; Oh, Jong-Min

    2015-01-01

    The feathers and diet items of grey heron (Ardea cinerea) and black-crowned night-heron (Nycticorax nycticorax) chicks were collected at the Pyeongtaek colony, Korea in 2002 and 2008, and Cd, Pb, Mn and Zn concentrations were measured. Cd and Zn concentrations were higher in both species in 2008 than 2002 and were higher in grey herons than black-crowned night-herons in 2002. In 2008, Cd concentrations were higher in black-crowned night-herons than grey herons; Zn concentrations did not differ between species. Pb and Mn concentrations did not differ between species; however, there were yearly differences. Cd, Pb and Zn concentrations of feathers and diet were significantly correlated when species and years were combined. However, the predictive power of these relationships was limited because of species and yearly differences. All heron chicks had concentrations of Cd (<2 μg/g dw) and Pb (<4 μg/g dw) consistent with background concentrations for wild birds. Mn and Zn concentrations were within the range reported for other heron and egret species.

  4. Piezoelectric Properties of Pb0.98Bi0.02Zr0.51Ti0.48Zn0.01O3 Ceramics

    NASA Astrophysics Data System (ADS)

    He, Wenze; Yu, Jian

    2011-02-01

    On the basis of eutectic behavior of PbTiO3-PbZrO3-Bi(Zn0.5Ti0.5)O3 ternary system, perovskite-structured Pb0.98Bi0.02Zr0.51Ti0.48Zn0.01O3 ceramics were able to be prepared using conventional electronic ceramic processing at low sintering temperature compatible with Ag as inner electrode materials, promising for co-firing technology to fabricate monolithic multilayer piezoelectric transducers. The dependence of its piezoelectric properties on sintering temperature and various dopants were investigated experimentally and a piezoelectric property with dielectric constant of ɛ33T/ɛ0=1190, dielectric loss of tan δ=0.6%, piezoelectric coefficient of d33=270 pC/N, planar coupling coefficient of kp=0.54, thickness coupling coefficient of kt=0.46 and Curie temperature of Tc=346 °C was obtained for the 0.5% Co-doped Pb0.98Bi0.02Zr0.51Ti0.48Zn0.01O3 ceramics sintered at 950 °C.

  5. From monomer to monolayer: a global optimisation study of (ZnO)n nanoclusters on the Ag surface.

    PubMed

    Demiroglu, Ilker; Woodley, Scott M; Sokol, Alexey A; Bromley, Stefan T

    2014-12-21

    We employ global optimisation to investigate how oxide nanoclusters of increasing size can best adapt their structure to lower the system energy when interacting with a realistic extended metal support. Specifically, we focus on the (ZnO)@Ag(111) system where experiment has shown that the infinite Ag(111)-supported ZnO monolayer limit corresponds to an epitaxially 7 : 8 matched graphene-like (Zn(3)O(3))-based hexagonal sheet. Using a two-stage search method based on classical interatomic potentials and then on more accurate density functional theory, we report global minina candidate structures for Ag-supported (ZnO)n cluster with sizes ranging from n = 1-24. Comparison with the respective global minina structure of free space (ZnO)n clusters reveals that the surface interaction plays a decisive role in determining the lowest energy Ag-supported (ZnO)n cluster structures. Whereas free space (ZnO)n clusters tend to adopt cage-like bubble structures as they grow larger, Ag-supported (ZnO)n clusters of increasing size become progressively more like planar cuts from the infinite graphene-like ZnO single monolayer. This energetic favourability for planar hexagonal Ag-supported clusters over their 3D counterparts can be partly rationalised by the ZnO-Ag(111) epitaxial matching and the increased number of close interactions with the Ag surface. Detailed analysis shows that this tendency can also be attributed to the capacity of 2D clusters to distort to improve their interaction with the Ag surface relative to more rigid 3D bubble cluster isomers. For the larger sized clusters we find that the adsorption energies and most stable structural types appear to be rather converged confirming that our study makes a bridge between the Ag-supported ZnO monomer and the infinite Ag-supported ZnO monolayer.

  6. Accumulation of Pb, Cd, Cu and Zn in plants and hyperaccumulator choice in Lanping lead-zinc mine area, China.

    PubMed

    Yanqun, Zu; Yuan, Li; Schvartz, Christian; Langlade, Laurent; Fan, Liu

    2004-06-01

    A field survey of higher terrestrial plants growing on Lanping lead-zinc mine, China were conducted to identify species accumulating exceptionally large concentrations of Pb, Cd, Cu and Zn of 20 samples of 17 plant species. Concentrations of Pb and Zn in soil and in plant were higher than that of Cu and Cd. Significant difference was observed among the average concentrations of four heavy metals in plants (except Cd and Cu) and in soil (except Pb and Zn) (P<0.05). For the enrichment coefficient of the four heavy metals in plant, the order of average was Pb. Between four heavy metals, only significant difference was observed between the enrichment coefficient average of Cd and Cu (P<0.05). The enrichment coefficients were higher than 1 in Llex plyneura and Rhododendron annae in Paomaping for Pb, Salix cathayana, L. plyneura and R. annae in Paomaping for Cd, and R. annae in Paomaping for Zn, respectively. Concentrations and enrichment coefficient of Pb, Cd and Zn of Rhododendron were higher than that of Gramimeae. Enrichment coefficient of Pb, Cd and Zn were bush>tree>herbaceous, and herbaceous grew in soil with the highest concentrations of four heavy metals. In different areas, the concentrations of Pb, Cd, Cu and Zn in plants and soils and enrichment coefficient were different. Plants in Paomaping had more accumulating ability to Pb, Cd and Zn, and plants in Jinfeng River had more accumulating ability to Cu. Six plant species, i.e. S. cathayana, Lithocarpus dealbatus, L. plyneura, Fargesia dura, Arundinella yunnanensis and R. annae in Paomaping, had high accumulation capacity. R. annae in Paomaping had hyperaccumulating capacity to Pb, Cd and Zn, L. plyneura to Pb and Cd, and S. cathayana to Cd, respectively. PMID:15031017

  7. Ag-In-Zn-S quantum dots for hybrid organic-inorganic solar cells

    NASA Astrophysics Data System (ADS)

    Kim, Eung-min; Ruankham, Pipat; Lee, Jae-hyeong; Hachiya, Kan; Sagawa, Takashi

    2016-02-01

    Quantum dots of (AgIn)xZn2(1-x)S2 (x = 0.6, 0.8, and 1.0) capped by oleylamine were prepared and applied for hybrid organic-inorganic solar cells consisting of glass-indium-tin-oxide/ZnO/(AgIn)xZn2(1-x)S2/poly(3-hexylthiophene)/MoO3/Ag. The short-circuit current density (Jsc) and open-circuit voltage (Voc) of the hybrid solar cells were measured, and we found a low power conversion efficiency (PCE) below 0.1%. From the incident photon-to-current efficiency (IPCE) profiles of the hybrid devices, there is no marked photocurrent generation from 350 to 700 nm, which is ascribed to the absorption region of (AgIn)xZn2(1-x)S2. To improve the photovoltaic performance, ligand substitution from oleylamine to pyridine was performed. The PCE of the hybrid cell using the pyridine-capped (AgIn)xZn2(1-x)S2 was improved twofold in terms of both Jsc and Voc as compared with that of the oleylamine-capped one. In particular, from the IPCE measurements, a remarkable (more than doubled) enhancement of photocurrent generation from 400 to 450 nm was observed with the pyridine-substituted nanoparticles.

  8. Ages and sources of components of Zn-Pb, Cu, precious metal, and platinum group element deposits in the goodsprings district, clark county, Nevada

    USGS Publications Warehouse

    Vikre, P.; Browne, Q.J.; Fleck, R.; Hofstra, A.; Wooden, J.

    2011-01-01

    The Goodsprings district, Clark County, Nevada, includes zinc-dominant carbonate replacement deposits of probable late Paleozoic age, and lead-dominant carbonate replacement deposits, copper ?? precious metal-platinum group element (PGE) deposits, and gold ?? silver deposits that are spatially associated with Late Triassic porphyritic intrusions. The district encompasses ??500 km2 although the distribution of all deposits has been laterally condensed by late Mesozoic crustal contraction. Zinc, Pb, and Cu production from about 90 deposits was ??160,000 metric tons (t) (Zn > Pb >> Cu), 2.1 million ounces (Moz) Ag, 0.09 Moz Au, and small amounts of PGEs-Co, V, Hg, Sb, Ni, Mo, Mn, Ir, and U-were also recovered. Zinc-dominant carbonate replacement deposits (Zn > Pb; Ag ?? Cu) resemble Mississippi Valley Type (MVT) Zn-Pb deposits in that they occur in karst and fault breccias in Mississippian limestone where the southern margin of the regional late Paleozoic foreland basin adjoins Proterozoic crystalline rocks of the craton. They consist of calcite, dolomite, sphalerite, and galena with variably positive S isotope compositions (??34S values range from 2.5-13%), and highly radiogenic Pb isotope compositions (206Pb/204Pb >19), typical of MVT deposits above crystalline Precambrian basement. These deposits may have formed when southward flow of saline fluids, derived from basinal and older sedimentary rocks, encountered thinner strata and pinch-outs against the craton, forcing fluid mixing and mineral precipitation in karst and fault breccias. Lead-dominant carbonate replacement deposits (Pb > Zn, Ag ?? Cu ?? Au) occur among other deposit types, often near porphyritic intrusions. They generally contain higher concentrations of precious metals than zinc-dominant deposits and relatively abundant iron oxides after pyrite. They share characteristics with copper ?? precious metal- PGE and gold ?? silver deposits including fine-grained quartz replacement of carbonate minerals in

  9. Evidence for microbial activity in the formation of carbonate-hosted Zn-Pb deposits

    NASA Astrophysics Data System (ADS)

    Kucha, H.; Raith, J.

    2009-04-01

    *Kucha H **Raith J *University of Mining and Metallurgy, Faculty of Geology, Geophysics and Environmental Protection, Mickiewicza 30, PL-30-059 Krakow, Poland. ** University of Leoben, Department of Applied Geosciences and Geophysics, A-8700 Leoben, Peter Tunner Str. 5, Austria Evidence for microbial activity in the formation of carbonate-hosted Zn-Pb deposits To date evaluation of bacterial processes in the formation of carbonate-hosted Zn-Pb deposits is largely based on sulphur isotope evidence. However, during a past few years, textural criteria, have been established, which support the bacterial origin of many of these deposits. This has received a strong support from micro-, and nano-textures of naturally growing bacterial films in a flooded tunnel within carbonates that host the Piquette Zn-Pb deposit (Druschel et al., 2002). Bacterial textures, micro- and nano textures found in carbonate-hosted Zn-Pb deposits are: i)wavy bacterial films up to a few mm thick to up to a few cm long composed of peloids, ii)semimassive agglomeration of peloids in the carbonate matrix, and iii)solitary peloids dispersed in the carbonate matrix. Peloids are usually composed of a distinct 50-90um core most often made up of Zn-bearing calcite surrounded by 30-60um thick dentate rim composed of ZnS. Etching of Zn-carbonate cores reveals 1 - 2um ZnS filaments, and numerous 15 to 90nm large ZnS nano-spheres (Kucha et al., 2005). In massive ore composite Zn-calcite - sphalerite peloids are entirely replaced by zinc sulphide, and form peloids ghosts within banded sulphide layers. Bacterially derived micro- and nano-textures have been observed in the following carbonate-hosted Zn-Pb deposits: 1)Irish-type Zn-Pb deposits. In the Navan deposit the basic sulphur is isotopically light bacteriogenic S (Fallick at al., 2001). This is corroborated by semimassive agglomerations of composite peloids (Zn-calcite-ZnS corona or ZnS core-melnikovite corona). Etching of Zn-calcite core reveals globular

  10. The green synthesis of Ag/ZnO in montmorillonite with enhanced photocatalytic activity

    NASA Astrophysics Data System (ADS)

    Sohrabnezhad, Sh.; Seifi, A.

    2016-11-01

    The Ag/ZnO-MMT nanocomposite was prepared using urtica dioica leaf extract. To improve the photocatalytic properties of ZnO-MMT nanocomposite, silver metal nanoparticles was deposited over nanocomposite. Zn(CH3COO)2, AgNO3 and Urtica dioica leaf extract were used as a zinc, silver precursor and reducing agent, respectively. The nanocomposite was characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), and ultraviolet-visible diffuse reflectance spectroscopy (DRS). The powder X-ray diffraction showed that Ag/ZnO nanoparticles located on the surface MMT layers. The diffuse reflectance spectra of nanocomposite indicated a strong surface plasmon resonance (SPR) absorption band in the visible region, resulting from metallic Ag nanoparticles. TEM image demonstrated the presence of silver nanoparticles with an average size of 2-4 nm over both MMT and flower-shape ZnO. The photocatalytic activity of nanocomposite was studied for destructive reaction methylene blue dye under visible light. In addition, the effects of different parameters such as amount of nanocomposite, concentration of the dye and pH of the solution were studied. The results showed that modiffication of ZnO-MMT nanocomposite with silver nanoparticles increased the percentage of discoloration methylene blue (MB) from 38.95 to 91.95. MMT matrix showed an important role in the reduction of recombination of electron-hole in nanocomposite.

  11. Surface plasmon resonance in nanostructured Ag incorporated ZnS films

    SciTech Connect

    Chalana, S. R.; Mahadevan Pillai, V. P.; Ganesan, V.

    2015-10-15

    Silver incorporated zinc sulfide thin films are prepared by RF magnetron sputtering technique and the influence of silver incorporation on the structural, optical and luminescence properties is analyzed using techniques like grazing incidence X-Ray diffraction (GIXRD), atomic force microscopy (AFM), field emission scanning electron microscopy (FESEM), energy dispersive X-ray spectroscopy (EDS), micro-Raman spectroscopy, UV-Vis spectroscopy and laser photoluminescence spectroscopy. XRD analysis presents hexagonal wurtzite structure for the films. A reduction of crystallinity of the films is observed due to Ag incorporation. The Raman spectral analysis confirms the reduction of crystallinity and increase of strain due to the Ag incorporation. AFM analysis reveals a rough surface morphology for the undoped film and Ag incorporation makes the films uniform, dense and smooth. A blue shift of band gap energy with increase in Ag incorporation is observed due to quantum confinement effect. An absorption band (450-650 nm region) due to surface plasmon resonance of the Ag clusters present in the ZnS matrix is observed for the samples with higher Ag incorporation. The complex dielectric constant, loss factor and distribution of volume and surface energy loss of the ZnS thin films are calculated. Laser photoluminescence measurements gives an intense bluish green emission from the ZnS films and a quenching of the PL emission is observed which can be due to the metal plasmonic absorption and non-radiative energy transfer due to Ag incorporation.

  12. Pb, Zn and Cd mobility, availability and fractionation in aged soil remediated by EDTA leaching.

    PubMed

    Udovic, Metka; Lestan, Domen

    2009-03-01

    Soil washing remediation techniques usually remove only the labile heavy metal (HM) species from the soil, leaving the residual ones in less available/mobile forms, thus disturbing the chemical equilibrium among different species of HM in the soil. Re-establishing such equilibrium and shifting HM back to more available/mobile chemical forms could occur after exposing the remediated soil to environmental abiotic (ageing) factors. Contaminated soil from a smelter site (Pb 4600 mg kg(-1), Zn 1800 mg kg(-1), Cd 30 mg kg(-1)) was leached with increasing EDTA concentrations (2.5, 5.0, 10.0, 20.0, 40.0 and 4-consecutive steps of 40.0 mmol EDTA kg(-1) of soil). A gradient of removed HM was reached: from 6% to 73% of initial Pb, from 3% to 23% of initial Zn and from 17% to 74% of initial Cd were removed. Repetitive temperature changes (105 degrees C and -20 degrees C) were used to mimic abiotic factors acting on residual HM after EDTA soil leaching in saturated soil at 10% and 90% of soil water holding capacity. Fractionation using sequential extractions, mobility, and phytoavailability of Pb, Zn and Cd and Pb oral bioavailability were determined for aged and non-aged soil. The ageing treatment consistently lowered HM phytoavailability in the original (non-leached) and all treated (chelant-leached) soils. However, Pb, Zn and Cd behaved differently from each other; Pb mobility increased, Cd mobility decreased, while Zn mobility did not change. The results indicate that abiotic (ageing) processes change the availability/mobility of residual HM in all leaching treatments and should thus be considered in final remediation effectivity evaluation.

  13. Electrically conductive nanostructured silver doped zinc oxide (Ag:ZnO) prepared by solution-immersion technique

    NASA Astrophysics Data System (ADS)

    Afaah, A. N.; Asib, N. A. M.; Aadila, A.; Mohamed, R.; Rusop, M.; Khusaimi, Z.

    2016-07-01

    p-type ZnO films have been fabricated on ZnO-seeded glass substrate, using AgNO3 as a source of silver dopant by facile solution-immersion. Cleaned glass substrate were seeded with ZnO by mist-atomisation, and next the seeded substrates were immersed in Ag:ZnO solution. The effects of Ag doping concentration on the Ag-doped ZnO have been investigated. The substrates were immersed in different concentrations of Ag dopant with variation of 0, 1, 3, 5 and 7 at. %. The surface morphology of the films was characterized by field emission scanning electron microscope (FESEM). In order to investigate the electrical properties, the films were characterized by Current-Voltage (I-V) measurement. FESEM micrographs showed uniform distribution of nanostructured ZnO and Ag:ZnO. Besides, the electrical properties of Ag-doped ZnO were also dependent on the doping concentration. The I-V measurement result indicated the electrical properties of 1 at. % Ag:ZnO thin film owned highest electrical conductivity.

  14. Electronic structures and optical properties for Ag-N-codoped ZnO nanotubes

    PubMed Central

    2013-01-01

    The structural and electronic/optical properties of pure and Ag-N-codoped (8,0) ZnO nanotubes have been studied using first-principles calculations in the framework of the local spin density approximation. The configurations for Zn atoms replaced by Ag atoms are p-type semiconductor materials, and the bandgap increases when N atoms are doped into ZnO nanotube configurations. The optical studies based on dielectric function and reflectivity indicate that new transition peaks in the visible light range are observed, which can be ascribed to the Ag and N doping. Furthermore, there is a red shift observed with the increase of N concentration. PMID:23981389

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

    PubMed

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

    2015-09-01

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

  16. Sedimentary model for the giant Broken Hill Pb-Zn deposit, Australia

    NASA Astrophysics Data System (ADS)

    Wright, John V.; Haydon, Robert C.; McConachy, Geoff W.

    1987-07-01

    During the past 15 years there has been increasing acceptance of a volcanic exhalative origin for the giant 300-Mt Broken Hill Pb-Zn orebody. Supposedly, silicic pyroclastic rock types have been identified in the host-rock succession, and because of an association with basic volcanics (amphibolites), comparison is made with Phanerozoic continental rifts. The orebody has also been described as distal and deep water. We report that the so-called silicic volcanic rocks are all normal clastic sediments. The metasedimentary succession (more than 5 km thick) is interpreted as a series of major continental, fluvio-deltaic, progradational wedges interfingering with marine transgressive cycles, deposited in a gradually deepening basin. Pb-Zn mineralization is hosted by shallow-marine sands that later became reservoirs for the metal-bearing brines. Basin formation, stratigraphic architecture, and Pb-Zn mineralization can all be interpreted in terms of concepts understood from studies of the development of younger sedimentary basins. The inference is that Pb-Zn mineralization was generated by compactive expulsion of metal-bearing brines during accumulation of the sedimentary pile. *Request reprints from McConachy

  17. Enhanced phytoextraction of Cu, Pb, Zn and Cd with EDTA and EDDS.

    PubMed

    Luo, Chunling; Shen, Zhenguo; Li, Xiangdong

    2005-03-01

    Chemically enhanced phytoextraction has been proposed as an effective approach to removing heavy metals from contaminated soil through the use of high biomass plants. Using pot experiments, the effects of the application of EDTA, EDDS and citric acid on the uptake of Cu, Pb, Zn and Cd by corn (Zea mays L. cv. Nongda 108) and bean (Phaseolus vulgaris L. white bean) plants were studied. The results showed that EDDS was more effective than EDTA at increasing the concentration of Cu in corn and beans. The application of 5 mmol kg-1 soil EDDS to soil significantly increased concentrations of Cu in shoots, with maximum levels of 2060 and 5130 mg kg-1 DW in corn and beans, respectively, which were 45- and 135-fold higher than that in the corresponding control plants to which chelate had not been applied. Concentrations of Zn in shoots were also higher in the plants treated with EDDS than in those treated with EDTA. For Pb and Cd, EDDS was less effective than EDTA. The maximum Cu phytoextraction was found with the EDDS treatment. The application of EDTA and EDDS also significantly increased the shoot-to-root ratios of the concentrations of Cu, Pb, Zn and Cd in both plant species. The results of metal extraction with chelates showed that EDDS was more efficient at solubilizing Cu and Zn than EDTA, and that EDTA was better at solubilizing Pb and Cd than EDDS.

  18. Study on structure and properties of CuZn40Pb alloy

    NASA Astrophysics Data System (ADS)

    Achiţei, D. C.; Minciună, M. G.; Vizureanu, P.; Sandu, A. V.; Cimpoeşu, R.; Istrate, B.

    2016-06-01

    The paper shows aspects about the behavior of Cu-Zn-Pb alloys a subjected to the temperatures variation and corrosion resistance in saline medium (sea water). The chemical composition was determined by spectral analysis on optical spectrometer, type Foundry Masters. The experiments are completed by a microstructure analysis made on scanning electronic microscope.

  19. Investigation of transport properties of ZnO/PbS heterojunction solar cells

    NASA Astrophysics Data System (ADS)

    Cheng, Yang; Whitaker, Michael D. C.; Whiteside, Vincent R.; Bumm, Lloyd A.; Sellers, Ian R.

    Lead sulfide (PbS) and lead selenide (PbSe) colloidal quantum dots (CQDs) are considered as a potential candidate material for solar cell applications due to their large band gap tunability range (0.5 to 1.7 eV) and cost-effective solution based processing. A series of Glass/ITO/ZnO/PbS/MoO3/Au heterojunction solar cells were processed and analyzed. A stable (reproducible) 2% conversion efficiency under 1-sun is achieved based on the result of J - V measurements. Absorbance and external quantum efficiency (EQE) measurements clearly show photo-generated carrier extraction from PbS active layers in the solar cell. However, a non-ideal J - V behavior is observed in current-voltage measurements. This behavior may be attributed to a high density of trap states at the QD surface or defect states at the PbS/ZnO or ITO/ZnO interfaces. C-V and Impedance spectroscopy measurements are used to study this unusual behavior. These techniques could also help probe the transport properties and limitation of these heterojunction solar cells. This research is funded through NASA EPSCoR program Award # NNX13AN101A.

  20. Extremely High Phosphate Sorption Capacity in Cu-Pb-Zn Mine Tailings

    PubMed Central

    Huang, Longbin; Li, Xiaofang; Nguyen, Tuan A. H.

    2015-01-01

    Elevated inorganic phosphate (Pi) concentrations in pore water of amended tailings under direct revegetation may cause toxicity in some native woody species but not native forbs or herb species, all of which are key constituents in target native plant communities for phytostabilizing base metal mine tailings. As a result, Pi sorption capacity has been quantified by a conventional batch procedure in three types of base metal mine tailings sampled from two copper (Cu)-lead (Pb)-zinc (Zn) mines, as the basis for Pi-fertiliser addition. It was found that the Pi-sorption capacity in the tailings and local soil was extremely high, far higher than highly weathered agricultural soils in literature, but similar to those of volcanic ash soils. The Langmuir P-sorption maximum was up to 7.72, 4.12, 4.02 and 3.62 mg P g-1 tailings, in the fresh tailings of mixed Cu-Pb-Zn streams (MIMTD7), the weathered tailings of mixed Cu-Pb-Zn streams (MIMTD5), EHM-TD (fresh Cu-stream, high magnetite content) and local soil (weathered shale and schist), respectively. Physicochemical factors highly correlated with the high Pi-sorption in the tailings were fine particle distribution, oxalate and dithionite-citrate-bicarbonate extractable Fe (FeO and Fed), oxalate-extractable Al and Mn, and the levels of soluble Cd and Zn, and total S and Fe. Large amounts of amorphous Fe oxides and oxyhydroxides may have been formed from the oxidation of pyritic materials and redox cycles of Fe-minerals (such as pyrite (FeS2), ankerite (Ca(Fe Mg)(CO3)2 and siderite (FeCO3), as indicated by the extractable FeO values. The likely formation of sparingly soluble Zn-phosphate in the Pb-Zn tailings containing high levels of Zn (from sphalerite ((Zn,Fe)S, ZnS, (Zn,Cd)S)) may substantially lower soluble Zn levels in the tailings through high rates of Pi-fertiliser addition. As a result, the possibility of P-toxicity in native plant species caused by the addition of soluble phosphate fertilizers would be minimal. PMID

  1. An asymmetric Zn//Ag doped polyaniline microparticle suspension flow battery with high discharge capacity

    NASA Astrophysics Data System (ADS)

    Wu, Sen; Zhao, Yongfu; Li, Degeng; Xia, Yang; Si, Shihui

    2015-02-01

    In this study, the effect of oxygen on the potential of reduced polyaniline (PANI) was investigated. In order to enhance the air oxidation of reduced PANI, several composites of PANI doped with co-catalysts were prepared, and a reasonable flow Zn//PANI suspension cell system was designed to investigate the discharge capacity of obtained PANI composite microparticle suspension cathodes. Compared with PANI doped with Cu2+, La+, Mn2+ and zinc protoporphyrin, Ag doped PANI composite at 0.90 weight percent doping of Ag gave the highest value of discharge capacity for the half-cell potential from the initial value to -0.20 V (vs. SCE). A comparison study on the electrochemical properties of both PANI and Ag doped PANI microparticle suspension was done by using cyclic voltammetry, AC Impedance. Due to partial utilization of Zn//air fuel cell, the discharge capacity for Ag doped PANI reached 470 mA h g-1 at the current density of 20 mA cm-2. At 15 mA cm-2, the discharge capacity even reached up to 1650 mA h g-1 after 220 h constant current discharge at the final discharge voltage of 0.65 V. This work demonstrates an effective and feasible approach toward obtaining high energy and power densities by a Zn//Ag-doped PANI suspension flow battery system combined with Zn//air fuel cell.

  2. Structural analysis of the epitaxial interface Ag/ZnO in hierarchical nanoantennas

    NASA Astrophysics Data System (ADS)

    Sanchez, John Eder; Santiago, Ulises; Benitez, Alfredo; Yacamán, Miguel José; González, Francisco Javier; Ponce, Arturo

    2016-10-01

    Detectors, photo-emitter, and other high order radiation devices work under the principle of directionality to enhance the power of emission/transmission in a particular direction. In order to understand such directionality, it is important to study their coupling mechanism of their active elements. In this work, we present a crystalline orientation analysis of ZnO nanorods grown epitaxially on the pentagonal faces of silver nanowires. The analysis of the crystalline orientation at the metal-semiconductor interface (ZnO/Ag) is performed with precession electron diffraction under assisted scanning mode. In addition, high resolution X-ray diffraction on a Bragg-Brentano configuration has been used to identify the crystalline phases of the arrangement between ZnO rods and silver nanowires. The work presented herein provides a fundamental knowledge to understand the metal-semiconductor behavior related to the receiving/transmitting mechanisms of ZnO/Ag nanoantennas.

  3. Carbonate-hosted nonsulphide Zn-Pb mineralization of southern British Columbia, Canada

    NASA Astrophysics Data System (ADS)

    Paradis, Suzanne; Keevil, Halley; Simandl, George J.; Raudsepp, Mati

    2015-12-01

    Many carbonate-hosted sulphide deposits in the Salmo district of southern British Columbia have near-surface Zn- and Pb-bearing iron oxide-rich gossans. The gossans formed when carbonate-hosted, base metal sulphides were subjected to intense supergene weathering processes and metals were liberated by the oxidation of sulphide minerals. Two types of supergene carbonate-hosted nonsulphide deposits, direct replacement (`red ore') and wallrock replacement (`white ore'), are present in the Salmo district. The direct replacement deposits formed by the oxidation of primary sulphides; the base metals passed into solution and were redistributed and trapped within the space occupied by the oxidized portion of the sulphide protore. Depending on the extent of replacement of the sulphides by Zn-, Pb- and Fe-bearing oxides, silicates, carbonates and phosphates, the resulting ore can be called `mixed' (sulphides and nonsulphides) or simply `nonsulphide'. The wallrock replacement deposits formed when base metals liberated by the oxidation of sulphides were transported by circulating supergene solutions down and/or away from the sulphides to form wallrock replacement deposits. The direct replacement nonsulphide zones of the Salmo district overlay the sulphide bodies in which they replaced the sulphides and carbonates, forming large irregular replacement masses, encrustations and open-space fillings. They consist predominantly of hematite, goethite, hemimorphite [Zn4Si2O7(OH)2·H2O], minor hydrozincite [Zn5(CO3)2(OH)6], cerussite [PbCO3] and traces of willemite [Zn2SiO4]. The wallrock replacement zones consist mainly of hemimorphite with local occurrences of iron oxides, hopeite [Zn3(PO4)2·4H2O] and tarbuttite [Zn2(PO4)(OH)]. No remnants of sulphides were observed in the replacement zones. The Salmo nonsulphide deposits were formed by prolonged weathering of Mississippi Valley-type (MVT) mineralization that underwent dissolution and oxidation of the pyrite, sphalerite and galena

  4. Thallium transformation and partitioning during Pb-Zn smelting and environmental implications.

    PubMed

    Liu, Juan; Wang, Jin; Chen, Yongheng; Xie, Xiaofan; Qi, Jianying; Lippold, Holger; Luo, Dinggui; Wang, Chunlin; Su, Longxiao; He, Lucheng; Wu, Qiwei

    2016-05-01

    Thallium (Tl) is a toxic and non-essential heavy metal. Raw Pb-Zn ores and solid smelting wastes from a large Pb-Zn smelting plant - a typical thallium (Tl) pollution source in South China, were investigated in terms of Tl distribution and fractionation. A modified IRMM (Institute for Reference Materials and Measurement, Europe) sequential extraction scheme was applied on the samples, in order to uncover the geochemical behavior and transformation of Tl during Pb-Zn smelting and to assess the potential environmental risk of Tl arising from this plant. Results showed that the Pb-Zn ore materials were relatively enriched with Tl (15.1-87.7 mg kg(-1)), while even higher accumulation existed in the electrostatic dust (3280-4050 mg kg(-1)) and acidic waste (13,300 mg kg(-1)). A comparison of Tl concentration and fraction distribution in different samples clearly demonstrated the significant role of the ore roasting in Tl transformation and mobilization, probably as a result of alteration/decomposition of related minerals followed by Tl release and subsequent deposition/co-precipitation on fine surface particles of the electrostatic dust and acidic waste. While only 10-30% of total Tl amounts was associated with the exchangeable/acid-extractable fraction of the Pb-Zn ore materials, up to 90% of total Tl was found in this fraction of the electrostatic dust and acidic waste. Taking into account the mobility and bioavailability of this fraction, these waste forms may pose significant environmental risk. PMID:26840520

  5. Comparison of serum Concentration of Se, Pb, Mg, Cu, Zn, between MS patients and healthy controls

    PubMed Central

    Alizadeh, Anahita; Mehrpour, Omid; Nikkhah, Karim; Bayat, Golnaz; Espandani, Mahsa; Golzari, Alireza; Jarahi, Lida; Foroughipour, Mohsen

    2016-01-01

    Introduction Multiple Sclerosis (MS) is defined as one of the inflammatory autoimmune disorders and is common. Its exact etiology is unclear. There are some evidences on the role of environmental factors in susceptible genetics. The aim of this study is to evaluate the possible role of Selenium, Zinc, Copper, Lead and Magnesium metals in Multiple Sclerosis patients. Methods In the present analytical cross-sectional study, 56 individuals including 26 patients and 30 healthy controls were enrolled in the evaluation. The serum level of Se, Zn, Cu, Pb were quantified in graphite furnace conditions and flame conditions by utilizing an atomic absorption Perkin Elmer spectrophotometer 3030. The serum levels of Mg were measured by auto analyzer 1500 BT. The mean level of minerals (Zn, Pb, Cu, Mg, Se) in serum samples were compared in both cases and controls. The mean level of minerals (Zn, Pb, Cu, Mg, Se) in serum samples were compared in both cases and controls by using independent-samples t-test for normal distribution and Mann-Whitney U test as a non-parametric test. All statistical analyses were carried out using SPSS 11.0. Results As well as the Zn, Cu, and Se, there was no significant difference between MS patients and healthy individuals in Pb concentrations (p-value = 0.11, 0.14, 0.32, 0.20 respectively) but the level of Mg was significantly different (p= 0.001). Conclusion All serum concentrations of Zn, Pb, Se, Cu in both groups were in normal ranges and there was no difference in MS patients compared with the healthy group who were matched in genetics. Blood level of Mg was significantly lower in MS patients. But it should be noted that even with the low level of serum magnesium in MS patients, this value is still in the normal range. PMID:27757186

  6. Thallium transformation and partitioning during Pb-Zn smelting and environmental implications.

    PubMed

    Liu, Juan; Wang, Jin; Chen, Yongheng; Xie, Xiaofan; Qi, Jianying; Lippold, Holger; Luo, Dinggui; Wang, Chunlin; Su, Longxiao; He, Lucheng; Wu, Qiwei

    2016-05-01

    Thallium (Tl) is a toxic and non-essential heavy metal. Raw Pb-Zn ores and solid smelting wastes from a large Pb-Zn smelting plant - a typical thallium (Tl) pollution source in South China, were investigated in terms of Tl distribution and fractionation. A modified IRMM (Institute for Reference Materials and Measurement, Europe) sequential extraction scheme was applied on the samples, in order to uncover the geochemical behavior and transformation of Tl during Pb-Zn smelting and to assess the potential environmental risk of Tl arising from this plant. Results showed that the Pb-Zn ore materials were relatively enriched with Tl (15.1-87.7 mg kg(-1)), while even higher accumulation existed in the electrostatic dust (3280-4050 mg kg(-1)) and acidic waste (13,300 mg kg(-1)). A comparison of Tl concentration and fraction distribution in different samples clearly demonstrated the significant role of the ore roasting in Tl transformation and mobilization, probably as a result of alteration/decomposition of related minerals followed by Tl release and subsequent deposition/co-precipitation on fine surface particles of the electrostatic dust and acidic waste. While only 10-30% of total Tl amounts was associated with the exchangeable/acid-extractable fraction of the Pb-Zn ore materials, up to 90% of total Tl was found in this fraction of the electrostatic dust and acidic waste. Taking into account the mobility and bioavailability of this fraction, these waste forms may pose significant environmental risk.

  7. Mass preparation and novel visible light photocatalytic activity of C and Ag Co-modified ZnO nanocrystals.

    PubMed

    Zhang, Xiao-Yan; Deng, Ya-Juan; Liu, Jin-Ku; Lu, Yi; Yang, Xiao-Hong

    2015-12-01

    A combustion method was developed to synthesize the C and Ag co-modified ZnO NCs to enhance its photocatalytic efficiency and practicability. The results showed that the doped Ag was significant to promote the photocatalytic activity, and the optimum content was 2% molar ratio of Ag to Zn atom. The degradation rate under visible light increased by 150% compared with C-ZnO NCs, while by more 1233.3% than pure ZnO photocatalyst. There were some new little particles with grain size about 10 nm on the C-ZnO NCs surface, which may state for the existence of Ag atoms. The synergy effect of Ag and carbon elements was proposed to explain the mechanism of enhanced photocatalytic performance under visible light irradiation. PMID:26254866

  8. Visible-light photocatalytic degradation of methylene blue with laser-induced Ag/ZnO nanoparticles

    NASA Astrophysics Data System (ADS)

    Whang, Thou-Jen; Hsieh, Mu-Tao; Chen, Huang-Han

    2012-01-01

    The preparation of Ag doped ZnO nanoparticles conducted through the method of laser-induction is presented in this work. The Ag/ZnO nanoparticles attained from various weight percentages of added AgNO3 relative to ZnO were applied under visible-light irradiation for evaluating the heterogeneous photocatalytic degradations of methylene blue (MB) solutions. It was shown that the catalytic behavior of Ag/ZnO nanoparticles in the visible-light range is notably improved through the Ag deposition onto ZnO nanoparticles by the method of laser-induction with a maximum effectiveness of 92% degradation. The properties of the nanoparticles were characterized by the employments of UV-vis spectroscopy (UV-vis), X-ray diffraction (XRD), transmission electron microscopy (TEM), energy dispersive X-ray spectroscopy (EDX), and selected-area electron diffraction (SAED).

  9. Ag nanoparticles-decorated ZnO nanorod array on a mechanical flexible substrate with enhanced optical and antimicrobial properties

    NASA Astrophysics Data System (ADS)

    Chen, Yi; Tse, Wai Hei; Chen, Longyan; Zhang, Jin

    2015-03-01

    Heteronanostructured zinc oxide nanorod (ZnO NR) array are vertically grown on polydimethylsiloxane (PDMS) through a hydrothermal method followed by an in situ deposition of silver nanoparticles (Ag NPs) through a photoreduction process. The Ag-ZnO heterostructured nanorods on PDMS are measured with an average diameter of 160 nm and an average length of 2 μm. ZnO NRs measured by high-resolution transmission electron microscope (HRTEM) shows highly crystalline with a lattice fringe of 0.255 nm, which corresponds to the (0002) planes in ZnO crystal lattice. The average diameter of the Ag NPs in situ deposited on the ZnO NRs is estimated at 22 ± 2 nm. As compared to the bare ZnO NRs, the heterostructured Ag-ZnO nanorod array shows enhanced ultraviolet (UV) absorption at 440 nm, and significant emission in the visible region (λem = 542 nm). In addition, the antimicrobial efficiency of Ag-ZnO heterostructured nanorod array shows obvious improvement as compared to bare ZnO nanorod array. The cytotoxicity of ZnO nanorod array with and without Ag NPs was studied by using 3 T3 mouse fibroblast cell line. No significant toxic effect is imposed on the cells.

  10. Ag/ZnO hybrid systems studied with scanning tunnelling microscopy-based luminescence spectroscopy

    NASA Astrophysics Data System (ADS)

    Pascua, Leandro; Stavale, Fernando; Nilius, Niklas; Freund, Hans-Joachim

    2016-03-01

    Coupled metal/oxide systems are prepared by depositing and embedding Ag nanoparticles into crystalline ZnO films grown on Au(111) supports. The morphology and optical properties of the compounds are investigated by topographic imaging and luminescence spectroscopy performed in a scanning tunnelling microscope (STM). The luminescence of bare ZnO is governed by the band-recombination and a Zn-vacancy related peak. After Ag deposition, two additional maxima are detected that are assigned to the in-plane and out-of-plane plasmon in Ag nanoparticles and have energies below and slightly above the oxide band-gap, respectively. Upon coating the particles with additional ZnO, the out-of-plane plasmon redshifts and loses intensity, indicating strong coupling to the oxide electronic system, while the in-plane mode broadens but remains detectable. The original situation can be restored by gently heating the sample, which drives the silver back to the surface. However, the optical response of pristine ZnO is not recovered even after silver evaporation at high temperature. Small discrepancies are explained with changes in the ZnO defect landscape, e.g., due to silver incorporation. Our experiments demonstrate how energy-transfer processes can be investigated in well-defined metal/oxide systems by means of STM-based spectroscopic techniques.

  11. Breakthrough of the p-type doping bottleneck in ZnO by inserting an ultrathin ZnX (X  =  S, Se and Te) layer doped with NX or AgZn

    NASA Astrophysics Data System (ADS)

    Jiang, Xin-he; Shi, Jun-jie; Zhang, Min; Zhong, Hong-xia; Huang, Pu; Ding, Yi-min; Cao, Xiong; Wu, Meng; Liao, Zhi-min

    2016-03-01

    The worldwide problem of p-type doping in ZnO is investigated based on first-principles calculations by combining the standard density functional theory and hybrid functional methods. We find that p-type doping can be realized by inserting an ultrathin ZnX (X  =  S, Se and Te) layer, doped with NX or AgZn, into ZnO to form short-period (ZnO) m /(ZnX) n (m  >  n) superlattices. The formation energy is the lowest for NX or AgZn in the ZnX layer. The Zn-rich (Zn-poor) condition is favourable for the formation of the NX (AgZn) defect. Compensation by the native defects can be avoided for the Ag-doped (ZnO) m /(ZnX) n under the Zn-poor condition. The N (Ag) acceptor activation energy can be reduced from 0.45 (0.43) eV in ZnO to 0.33 (0.32) eV in (ZnO)5/(ZnS)1, 0.20 (0.24) eV in (ZnO)5/(ZnSe)1 and 0.12 (0.13) eV in (ZnO)5/(ZnTe)1, which is caused by the ZnX-monolayer modulation to the local structure around the NX or AgZn defect and the high-lying p-derived valence bands. Moreover, the band gaps can be tuned from 3.40 eV of ZnO to 3.21 eV of (ZnO)5/(ZnS)1, 2.41 eV of (ZnO)5/(ZnSe)1 and 2.26 eV of (ZnO)5/(ZnTe)1, which is promising for the integration of ZnO-based white light-emitting diodes.

  12. Uptake and accumulation of potentially toxic metals (Zn, Cu and Pb) in soils and plants of Durgapur industrial belt.

    PubMed

    Kisku, Ganesh Chandra; Pandey, Poonam; Negi, Mahendra Pratap Singh; Misra, Virendra

    2011-11-01

    Uptake and accumulation of metals in crops may cause possible health risks through food chain. A field survey was conducted to investigate the accumulation of potentially toxic metals contamination in soil and plants irrigated with complexed industrial effluents. Concentration of Zn, Cu and Pb was 205-255,101-130,118-177 microg g(-1) in rhizosphere soils and 116-223, 57-102 and 63-95 microg g(-1) d. wt. in root and 95-186, 44-75 and 27-58 microg g(-1) d. wt. in shoot, respectively. The trend in Cu and Pb was in the order: soil > root > shoot > seed while in Zn it was soil > root > seed > shoot. Roots accumulated a larger fraction of soil Cu (70%) > Zn (67%) > Pb (54%). Bioaccumulation coefficient of soil to root ranged from 51-98 for Zn, 54-85 for Cu and 43-63 for Pb.Analysis of variance showed marginal change in bioaccumulation coefficient, noticed between plants (p > 0.05) while it varied significantly (p < 0.01) between tissues and metals. It increased from root to seed/fruit (root > shoot > seed/fruit) while decreased between metals from Zn to Pb (Zn > Cu > Pb). Out of the three, two Cu and Pb accumulated to phyotoxic levels while Zn was within threshold limit of phytotoxicity. PMID:22471223

  13. Tyrosine-assisted preparation of Ag/ZnO nanocomposites with enhanced photocatalytic performance and synergistic antibacterial activities

    NASA Astrophysics Data System (ADS)

    Lu, Weiwei; Liu, Guosheng; Gao, Shuyan; Xing, Shantao; Wang, Jianji

    2008-11-01

    In this paper, Ag/ZnO metal-semiconductor nanocomposites were prepared through a facile one-pot hydrothermal method with the assistance of tyrosine. The synthesized samples were structurally characterized by x-ray diffraction, scanning electron microscope, transmission electron microscope and x-ray photoelectron spectroscopy. It was shown that the added tyrosine served both as a shape conductor for the formation of ZnO faceted nanorods and as a reducing agent of Ag+ ions. In the reaction process, the complexation of Ag+ with NH3 and OH- decreased the redox potential of Ag+/Ag, which prevented the formation of isolated Ag nanoparticles in solution. The prepared Ag/ZnO nanocomposites showed potential applications in photodegradation of organic dye pollutants and destruction of bacteria.

  14. Enhanced photocatalytic performance of sandwiched ZnO@Ag@Cu2O nanorod films: the distinct role of Ag NPs in the visible light and UV region

    NASA Astrophysics Data System (ADS)

    Ren, Shoutian; Zhao, Guoliang; Wang, Yingying; Wang, Benyang; Wang, Qiang

    2015-03-01

    Sandwiched ZnO@Ag@Cu2O nanorod films were synthesized by successive electrodeposition, magnetron sputtering and the second electrodeposition. The as-synthesized composites were characterized by x-ray diffraction patterns, field emission scanning electron microscopy, low- and high-resolution transmission electron microscopy and a UV-vis spectrophotometer. Their photocatalytic performance was estimated by the degradation of a methyl orange solution under UV or visible-light irradiation, respectively. In the visible region, due to localized surface plasmon resonance absorption of Ag NPs, ZnO@Ag@Cu2O showed a significantly enhanced photocatalytic performance. The enhancement factor of Ag NPs on the catalytic performance of ZnO@Ag@Cu2O was estimated as a function of the Cu2O deposition time, and the corresponding enhancement mechanism was also evaluated by the monochromatic photocatalytic experiment and discrete dipole approximation simulation. In the UV region, due to the formation of a Schottky junction (e.g. Ag/ZnO, Ag/Cu2O), a limited enhanced photocatalytic performance was also realized for ZnO@Ag@Cu2O photocatalysts.

  15. Synergistic effects of dual Zn/Ag ion implantation in osteogenic activity and antibacterial ability of titanium.

    PubMed

    Jin, Guodong; Qin, Hui; Cao, Huiliang; Qian, Shi; Zhao, Yaochao; Peng, Xiaochun; Zhang, Xianlong; Liu, Xuanyong; Chu, Paul K

    2014-09-01

    Zinc (Zn) and silver (Ag) are co-implanted into titanium by plasma immersion ion implantation. A Zn containing film with Ag nanoparticles (Ag NPs) possessing a wide size distribution is formed on the surface and the corrosion resistance is improved due to the micro-galvanic couples formed by the implanted Zn and Ag. Not only are the initial adhesion, spreading, proliferation and osteogenic differentiation of rBMSCs observed from the Zn/Ag implanted Ti in vitro, but also bacteria killing is achieved both in vitro and in vivo. Electrochemical polarization and ion release measurements suggest that the excellent osteogenic activity and antibacterial ability of the Zn/Ag co-implanted titanium are related to the synergistic effect resulting from the long-range interactions of the released Zn ions and short-range interactions of the embedded Ag NPs. The Zn/Ag co-implanted titanium offers both excellent osteogenic activity and antibacterial ability and has large potential in orthopedic and dental implants. PMID:24947228

  16. Synergistic effects of dual Zn/Ag ion implantation in osteogenic activity and antibacterial ability of titanium.

    PubMed

    Jin, Guodong; Qin, Hui; Cao, Huiliang; Qian, Shi; Zhao, Yaochao; Peng, Xiaochun; Zhang, Xianlong; Liu, Xuanyong; Chu, Paul K

    2014-09-01

    Zinc (Zn) and silver (Ag) are co-implanted into titanium by plasma immersion ion implantation. A Zn containing film with Ag nanoparticles (Ag NPs) possessing a wide size distribution is formed on the surface and the corrosion resistance is improved due to the micro-galvanic couples formed by the implanted Zn and Ag. Not only are the initial adhesion, spreading, proliferation and osteogenic differentiation of rBMSCs observed from the Zn/Ag implanted Ti in vitro, but also bacteria killing is achieved both in vitro and in vivo. Electrochemical polarization and ion release measurements suggest that the excellent osteogenic activity and antibacterial ability of the Zn/Ag co-implanted titanium are related to the synergistic effect resulting from the long-range interactions of the released Zn ions and short-range interactions of the embedded Ag NPs. The Zn/Ag co-implanted titanium offers both excellent osteogenic activity and antibacterial ability and has large potential in orthopedic and dental implants.

  17. Metal and metalloid contamination in roadside soil and wild rats around a Pb-Zn mine in Kabwe, Zambia.

    PubMed

    Nakayama, Shouta M M; Ikenaka, Yoshinori; Hamada, Kyohei; Muzandu, Kaampwe; Choongo, Kennedy; Teraoka, Hiroki; Mizuno, Naoharu; Ishizuka, Mayumi

    2011-01-01

    Metal (Cr, Co, Cu, Zn, Cd, Pb, Ni) and metalloid (As) accumulation was studied in roadside soil and wild rat (Rattus sp.) samples from near a Pb-Zn mine (Kabwe, Zambia) and the capital city of Zambia (Lusaka). The concentrations of the seven metals and As in the soil samples and Pb in the rat tissue samples were quantified using atomic absorption spectroscopy. The concentrations of Pb, Zn, Cu, Cd, and As in Kabwe soil were much higher than benchmark values. Geographic Information System analysis indicated the source of metal pollution was mining and smelting activity. Interestingly, the area south of the mine was more highly contaminated even though the prevailing wind flow was westward. Wild rats from Kabwe had much higher tissue concentrations of Pb than those from Lusaka. Their body weight and renal Pb levels were negatively correlated, which suggests that mining activity might affect terrestrial animals in Kabwe. PMID:20971538

  18. Metal and metalloid contamination in roadside soil and wild rats around a Pb-Zn mine in Kabwe, Zambia.

    PubMed

    Nakayama, Shouta M M; Ikenaka, Yoshinori; Hamada, Kyohei; Muzandu, Kaampwe; Choongo, Kennedy; Teraoka, Hiroki; Mizuno, Naoharu; Ishizuka, Mayumi

    2011-01-01

    Metal (Cr, Co, Cu, Zn, Cd, Pb, Ni) and metalloid (As) accumulation was studied in roadside soil and wild rat (Rattus sp.) samples from near a Pb-Zn mine (Kabwe, Zambia) and the capital city of Zambia (Lusaka). The concentrations of the seven metals and As in the soil samples and Pb in the rat tissue samples were quantified using atomic absorption spectroscopy. The concentrations of Pb, Zn, Cu, Cd, and As in Kabwe soil were much higher than benchmark values. Geographic Information System analysis indicated the source of metal pollution was mining and smelting activity. Interestingly, the area south of the mine was more highly contaminated even though the prevailing wind flow was westward. Wild rats from Kabwe had much higher tissue concentrations of Pb than those from Lusaka. Their body weight and renal Pb levels were negatively correlated, which suggests that mining activity might affect terrestrial animals in Kabwe.

  19. Competitive sorption of Cd, Cu, Mn, Ni, Pb and Zn in polluted and unpolluted calcareous soils.

    PubMed

    Jalali, Mohsen; Moradi, Fahimeh

    2013-11-01

    The objectives of this study were to investigate competitive sorption behaviour of heavy metals (Cd, Cu, Mn, Ni, Pb and Zn) under different management practices and identify soil characteristics that can be correlated with the retention and mobility of heavy metals using 65 calcareous soil samples. The lowest sorption was found for Mn and Ni in competition with the other metals, indicating the high mobility of these two cations. The Freundlich equation adequately described heavy metals adsorption. On the basis of Freundlich distribution coefficient, the selectivity sequence of the metal adsorption was Cu > Pb > Cd > Zn > Ni > Mn. The mean value of the joint distribution coefficient (K dΣsp) was 182.1, 364.1, 414.7, 250.1, 277.7, 459.9 and 344.8 l kg(-1) for garden, garlic, pasture, potato, vegetables, wheat and polluted soils, respectively. The lowest observed K dΣsp in garden soil samples was due to the lower cation exchange capacity and lower carbonate content. The results of the geochemical modelling under low and high metal addition indicated that Cd, Ni, Mn and Zn were mainly retained via adsorption, while Pb and Cu were retained via adsorption and precipitation. Stepwise forward regression analysis showed that clay, organic matter and CaCO3 were the most important soil properties influencing competitive adsorption of Cd, Mn, Ni and Zn. The results in this study point to a relatively easy way to estimate distribution coefficient values. PMID:23677680

  20. Use of cattails in treating wastewater from a Pb/Zn mine

    NASA Astrophysics Data System (ADS)

    Lan, Chongyu; Chen, Guizhu; Li, Liuchun; Wong, M. H.

    1992-01-01

    This article describes the use of a combined treatment system, which includes an aquatic treatment pond with Typha latifolia Linn. (Typhaceae) as the dominant species and a stabilization pond, to treat the wastewater from a Pn/Zn mine at Shaoguan, Guangdong Province, China. In 1983, it was noted that T. latifolia bloomed in areas affected by the wastewater emitted from the mine, hence a combined purification system was subsequently built. The influent contained high levels of total suspended solids (4635 mg/liter), chemical oxygen demand (14.5 mg/liter) as well as Pb (1.6 mg/liter) and Zn (1.9 mg/liter). The results of the effluent after treatment showed that the total suspended solids, chemical oxygen demand, Pb, and Zn had been reduced by 99%, 55%, 95%, and 80% respectively. The results of plant tissue analysis indicled that T. latifolia assimilated significant amounts of Pb and Zn, especially in the root portion. During 1986 several species of algae and fish were present in the pond, usually with a higher density in areas containing lower metal concentrations in the water.

  1. Co-doping of Ag into Mn:ZnSe Quantum Dots: Giving Optical Filtering effect with Improved Monochromaticity

    PubMed Central

    Hu, Zhiyang; Xu, Shuhong; Xu, Xiaojing; Wang, Zhaochong; Wang, Zhuyuan; Wang, Chunlei; Cui, Yiping

    2015-01-01

    In optics, when polychromatic light is filtered by an optical filter, the monochromaticity of the light can be improved. In this work, we reported that Ag dopant atoms could be used as an optical filter for nanosized Mn:ZnSe quantum dots (QDs). If no Ag doping, aqueous Mn:ZnSe QDs have low monochromaticity due to coexisting of strong ZnSe band gap emission, ZnSe trap emission, and Mn dopant emission. After doping of Ag into QDs, ZnSe band gap and ZnSe trap emissions can be filtered, leaving only Mn dopant emission with improved monochromaticity. The mechanism for the optical filtering effect of Ag was investigated. The results indicate that the doping of Ag will introduce a new faster deactivation process from ZnSe conduction band to Ag energy level, leading to less electrons deactived via ZnSe band gap emission and ZnSe trap emission. As a result, only Mn dopant emission is left. PMID:26446850

  2. Leaching potential of pervious concrete and immobilization of Cu, Pb and Zn using pervious concrete.

    PubMed

    Solpuker, U; Sheets, J; Kim, Y; Schwartz, F W

    2014-06-01

    This paper investigates the leaching potential of pervious concrete and its capacity for immobilizing Cu, Pb and Zn, which are common contaminants in urban runoff. Batch experiments showed that the leachability of Cu, Pb and Zn increased when pH<8. According to PHREEQC equilibrium modeling, the leaching of major ions and trace metals was mainly controlled by the dissolution/precipitation and surface complexation reactions, respectively. A 1-D reactive transport experiment was undertaken to better understand how pervious concrete might function to attenuate contaminant migration. A porous concrete block was sprayed with low pH water (pH=4.3±0.1) for 190 h. The effluent was highly alkaline (pH~10 to 12). In the first 50 h, specific conductance and trace-metal were high but declined towards steady state values. PHREEQC modeling showed that mixing of interstitial alkaline matrix waters with capillary pore water was required in order to produce the observed water chemistry. The interstitial pore solutions seem responsible for the high pH values and relatively high concentrations of trace metals and major cations in the early stages of the experiment. Finally, pervious concrete was sprayed with a synthetic contaminated urban runoff (10 ppb Cu, Pb and Zn) with a pH of 4.3±0.1 for 135 h. It was found that Pb immobilization was greater than either Cu or Zn. Zn is the most mobile among three and also has the highest variation in the observed degree of immobilization.

  3. Magnetic properties of ZnS doped with noble metals (X = Ru, Rh, Pd, and Ag)

    NASA Astrophysics Data System (ADS)

    Tan, Zhiyun; Xiao, Wenzhi; Wang, Lingling; Yang, Youchang

    2012-12-01

    Density functional theory calculations are carried out to study the electronic structures and magnetic properties in zinc-blende structure ZnS doped with nonmagnetic noble metals (X = Ru, Rh, Pd, and Ag). Results show robust magnetic ground states for X-doped ZnS. The total magnetic moments are about 2.0, 3.0, and 2.0 μB per supercell for the Ru-, Rh-, and Pd-doped ZnS, respectively. As the atomic number of X element increases, the local magnetic moment tends toward delocalize and the hybridization between X-4d and S-3p states become stronger. This trend is strongly related to the difference in electronegativity between the substitutional X and the cation in the ZnS host. For Ag-doped ZnS, both non-spin- and spin-polarized calculations yield nearly equal total energy. The substitution of Zn in ZnS parent material by the nonmagnetic 4d transition-metals may lead to half-metallic ferromagnetism which stems from the hybridization between X-4d and S-3p states and could be attributed to a double-exchange mechanism. Curie temperature values are estimated using mean-field approximation.

  4. Superhydrophobic Ag decorated ZnO nanostructured thin film as effective surface enhanced Raman scattering substrates

    NASA Astrophysics Data System (ADS)

    Jayram, Naidu Dhanpal; Sonia, S.; Poongodi, S.; Kumar, P. Suresh; Masuda, Yoshitake; Mangalaraj, D.; Ponpandian, N.; Viswanathan, C.

    2015-11-01

    The present work is an attempt to overcome the challenges in the fabrication of super hydrophobic silver decorated zinc oxide (ZnO) nanostructure thin films via thermal evaporation process. The ZnO nanowire thin films are prepared without any surface modification and show super hydrophobic nature with a contact angle of 163°. Silver is further deposited onto the ZnO nanowire to obtain nanoworm morphology. Silver decorated ZnO (Ag@ZnO) thin films are used as substrates for surface enhanced Raman spectroscopy (SERS) studies. The formation of randomly arranged nanowire and silver decorated nanoworm structure is confirmed using FESEM, HR-TEM and AFM analysis. Crystallinity and existence of Ag on ZnO are confirmed using XRD and XPS studies. A detailed growth mechanism is discussed for the formation of the nanowires from nanobeads based on various deposition times. The prepared SERS substrate reveals a reproducible enhancement of 3.082 × 107 M for Rhodamine 6G dye (R6G) for 10-10 molar concentration per liter. A higher order of SERS spectra is obtained for a contact angle of 155°. Thus the obtained thin films show the superhydrophobic nature with a highly enhanced Raman spectrum and act as SERS substrates. The present nanoworm morphology shows a new pathway for the construction of semiconductor thin films for plasmonic studies and challenges the orderly arranged ZnO nanorods, wires and other nano structure substrates used in SERS studies.

  5. ZnO-(Cu/Ag)TCNQ heterostructure network over flexible platform for enhanced cold cathode application

    NASA Astrophysics Data System (ADS)

    Pal, Shreyasi; Maiti, Soumen; Narayan Maiti, Uday; Chattopadhyay, Kalyan Kumar

    2016-07-01

    Multistage field emitters consisting of organic/inorganic hybrid nanostructures with branched geometry are designed via a two-step protocol: a simple wet chemical method followed by a vapor-solid-phase technique. (Cu/Ag)TCNQ (copper/silver-7,7,8,8-tetracyanoquinodimethane) nanowires (NWs) were grown hierarchically on zinc oxide (ZnO) nanorods (NRs) to form ZnO-(Cu/Ag)TCNQ heterostructure assemblies. By monitoring the metallic Cu and Ag coating thickness on ZnO NRs, precise control over the morphology and orientations of the secondary organic NWs is achieved. In-depth analysis of electron field emission (FE) behavior of the ZnO-(Cu/Ag)TCNQ-based hierarchy suggests highest emission performance with low turn-on as well as threshold fields of 1.15 and 3.75 V μm-1 respectively from the morphology-optimized hierarchy. Beneficial orientation of the branched organic NWs ensures sequential electric field enhancement in the consecutive stem and branches whereas its low work function eases electron emission; these aspects combined together render an overall enhancement in the emission behavior of the hybrid system. As compared to individual building units, the heterostructures show improved field electron emission. Additionally, successful construction of this novel hybrid over a fabric platform displays great potential in opening up new pathways in the highly-anticipated field of flexible electronics.

  6. 3D Ag/ZnO hybrids for sensitive surface-enhanced Raman scattering detection

    NASA Astrophysics Data System (ADS)

    Huang, Chenyue; Xu, Chunxiang; Lu, Junfeng; Li, Zhaohui; Tian, Zhengshan

    2016-03-01

    To combine the surface plasma resonance of metal and local field enhancement in metal/semiconductor interface, Ag nanoparticles (NPs) were assembled on a ZnO nanorod array which was grown by hydrothermally on carbon fibers. The construction of dimensional (3D) Surface-Enhanced Raman Scattering (SERS) substrate is used for the sensitive detection of organic pollutants with the advantages such as facile synthesis, short detection time and low cost. The hybrid substrate was manifested a high sensitivity to phenol red at a lower concentration of 1 × 10-9 M and a higher enhancement factor of 3.18 × 109. Moreover, the ZnO nanostructures decorated with Ag NPs were demonstrated self-cleaning function under UV irradiation via photocatalytic degradation of the analytic molecules. The fabrication process of the materials and sensors, optimization of the SERS behaviors for different sized Ag NPs, the mechanism of SERS and recovery were presented with a detailed discussion.

  7. Facile synthesis of Ag/ZnO heterostructures assisted by UV irradiation: Highly photocatalytic property and enhanced photostability

    SciTech Connect

    Yang, Zhongmei; Zhang, Ping; Ding, Yanhuai; Jiang, Yong; Long, Zhilin; Dai, Wenli

    2011-10-15

    Highlights: {yields} Fabrication of Ag/ZnO heterostructure between the two incompatible phases is realized under UV irradiation in the absence of surfactant. {yields} The synthetic method is facile, low cost, and low carbon, which depends on the photogenerated electrons produced by ZnO under UV light. {yields} Photocatalytic property of the as-synthesized samples is 3.0 times as good as the pure ZnO synthesized under the same condition or the commercial TiO{sub 2} (Degussa, P-25). {yields} The heterostructures exhibit good durability without significant change in the activity even after the third cycle compared to the pure ZnO. -- Abstract: We report a new method to synthesize Ag/ZnO heterostructures assisted by UV irradiation. The formation of Ag/ZnO heterostructures depends on photogenerated electrons produced by ZnO under UV light to reduce high valence silver. Functional property of the Ag/ZnO heterostructures is evaluated by photodegradation of methylene blue (MB) under UV illumination. Results of photodegradation tests reveal that the optimal photocatalytic activity of as-syntheszied samples is about 1.5 times higher than the pure ZnO synthesized in the same condition or commercial TiO{sub 2} (P-25), showing the advantage of the unique structure in the Ag/ZnO heterostructure. Besides, due to the reduced activation of surface oxygen atom, photocatalytic activity of the photocatalysts has no evident decrease even after three recycles.

  8. Ag- and Mn-doped ZnInS/ZnS dual-emission quantum dots with zone tunability in the color coordinate.

    PubMed

    Huang, Guangguang; Wang, Chunlei; Xu, Shuhong; Qi, Zhengqing; Lu, Changgui; Cui, Yiping

    2016-05-01

    In this work, we used Ag- and Mn-doped ZnInS/ZnS quantum dots (QDs) acting as a new generation of nontoxic dual-emission QDs with simultaneous tunable emission wavelengths and dual-emission ratiometric, which makes nontoxic dual-emission QDs with broad zone tunability in the color coordinate. The Ag-doped ZnInS ternary QDs can give rise to largely tunable emission wavelengths from 497 nm to 631 nm. The ratiometric of Ag and Mn dual emissions can be tuned by controlling Ag–Mn and Mn–Mn dopant coupling. With increased Mn doping amount, the increased Ag–Mn dopant coupling leads to increased Mn emission at the expense of lowered Ag emission and Ag fluorescence lifetime. The Mn–Mn coupling can be controlled by using different doping manners: co-doping Ag and Mn in ZnInS core or separate-doping Ag in ZnInS core and Mn in ZnS shell. Compared with co-doping, separate doping has weaker Mn–Mn interactions, an increased Mn irradiative recombination rate constant, and bright Mn photoluminescence.

  9. Schottky or Ohmic metal-semiconductor contact: influence on photocatalytic efficiency of Ag/ZnO and Pt/ZnO model systems.

    PubMed

    Yan, Fengpo; Wang, Yonghao; Zhang, Jiye; Lin, Zhang; Zheng, Jinsheng; Huang, Feng

    2014-01-01

    The relationship between the contact type in metal-semiconductor junctions and their photocatalytic efficiencies is investigated. Two metal-semiconductor junctions, silver on zinc oxide (Ag/ZnO) and platinum on zinc oxide (Pt/ZnO) serve as model system for Ohmic and Schottky metal-semiconductor contact, respectively. Ag/ZnO, with Ohmic contact, exhibits a higher photocatalytic efficiency than Pt/ZnO, with Schottky contact. The direction of electric fields within the semiconductor is found to play a crucial role in the separation of photogenerated charges, and thus strongly influences the photocatalytic efficiency.

  10. Air-Stable and Efficient PbSe Quantum-Dot Solar Cells Based upon ZnSe to PbSe Cation-Exchanged Quantum Dots.

    PubMed

    Kim, Sungwoo; Marshall, Ashley R; Kroupa, Daniel M; Miller, Elisa M; Luther, Joseph M; Jeong, Sohee; Beard, Matthew C

    2015-08-25

    We developed a single step, cation-exchange reaction that produces air-stable PbSe quantum dots (QDs) from ZnSe QDs and PbX2 (X = Cl, Br, or I) precursors. The resulting PbSe QDs are terminated with halide anions and contain residual Zn cations. We characterized the PbSe QDs using UV-vis-NIR absorption, photoluminescence quantum yield spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, and transmission electron microscopy. Solar cells fabricated from these PbSe QDs obtained an overall best power conversion efficiency of 6.47% at one sun illumination. The solar cell performance without encapsulation remains unchanged for over 50 days in ambient conditions; and after 50 days, the National Renewable Energy Laboratory certification team certified the device at 5.9%.

  11. Internally consistent database for sulfides and sulfosalts in the system Ag 2S-Cu 2S-ZnS-FeS-Sb 2S 3-As 2S 3: Update

    NASA Astrophysics Data System (ADS)

    Sack, Richard O.

    2005-03-01

    The thermodynamic database for Ag 2S-Cu 2S-ZnS-FeS-Sb 2S 3-As 2S 3 sulfides and sulfosalts applicable to temperatures above 119°C has been updated based on the results of recent petrologic, experimental, and theoretical studies. Solution and end-member properties of fahlore [˜(Ag,Cu) 10(Fe,Zn) 2(Sb,As) 4S 13] have been adjusted to allow for (1) revisions of the description of Fe-Zn partitioning with sphalerite that incorporate sphalerite activity-composition relations derived from the cluster variation method (CVM) model of a previous study, (2) the assumption that the miscibility gaps observed in high-Ag fahlores from the Husky Mine (Yukon, Canada) approximate a temperature of 170°C, and (3) an increase in the Ag-Cu partitioning between fahlore and polybasite (Ag,Cu) 16(Sb,As) 2S 11 required to reproduce compositions of fahlore in the polybasite + Sb-fahlore + ZnS sphalerite assemblage reported in previous experimental studies. The resulting minor parameter adjustments produce a database that demonstrably reproduces the composition data reported for a wide-range of sulfide ore deposits. They result in revised estimates for the Gibbs energies of formation of end-member fahlore components from the simple sulfides that, except for Cu 10Zn 2Sb 4S 13, are less temperature dependent than those previously inferred (at 200 and 400°C: -23.27 and -24.84 kJ/gfw for Ag 10Zn 2Sb 4S 13, -115.18 and -116.57 kJ/gfw for Cu 10Zn 2Sb 4S 13, -85.14 and -75.20 kJ/gfw for Cu 10Fe 2Sb 4S 13, and -3.81 and 9.10 kJ/gfw for Ag 10Fe 2Sb 4S 13). The database is extended to PbS-bearing supersystems containing the galena + fahlore + sphalerite assemblage. Predicted initial Ag-contents of galena calculated from this database agree with those inferred from petrological studies of Ag-Pb-Zn ores from the Coeur d'Alene district, Idaho, USA and Julcani, Peru.

  12. Impact of ZnO and Ag Nanoparticles on Bacterial Growth and Viability

    NASA Astrophysics Data System (ADS)

    Olson, M. S.; Digiovanni, K. A.

    2007-12-01

    Hundreds of consumer products containing nanomaterials are currently available in the U.S., including computers, clothing, cosmetics, sports equipment, medical devices and product packaging. Metallic nanoparticles can be embedded in or coated on product surfaces to provide antimicrobial, deodorizing, and stain- resistant properties. Although these products have the potential to provide significant benefit to the user, the impact of these products on the environment remains largely unknown. The purpose of this project is to study the effect of metallic nanoparticles released to the environment on bacterial growth and viability. Inhibition of bacterial growth was tested by adding doses of suspended ZnO and Ag nanoparticles into luria broth prior to inoculation of Escherichia coli cells. ZnO particles (approximately 40 nm) were obtained commercially and Ag particles (12-14 nm) were fabricated by reduction of silver nitrate with sodium borohydride. Toxicity assays were performed to test the viability of E. coli cells exposed to both ZnO and Ag nanoparticles using the LIVE/DEAD BacLight bacterial viability kit (Invitrogen). Live cells stain green whereas cells with compromised membranes that are considered dead or dying stain red. Cells were first grown, stained, and exposed to varying doses of metallic nanoparticles, and then bacterial viability was measured hourly using fluorescence microscopy. Results indicate that both ZnO and Ag nanoparticles inhibit the growth of E. coli in liquid media. Preliminary results from toxicity assays confirm the toxic effect of ZnO and Ag nanoparticles on active cell cultures. Calculated death rates resulting from analyses of toxicity studies will be presented.

  13. Growth and characterization of ZnO multipods on functional surfaces with different sizes and shapes of Ag particles

    NASA Astrophysics Data System (ADS)

    A, Kamalianfar; S, A. Halim; Mahmoud Godarz, Naseri; M, Navasery; Fasih, Ud Din; J, A. M. Zahedi; Kasra, Behzad; K, P. Lim; A Lavari, Monghadam; S, K. Chen

    2013-08-01

    Three-dimensional ZnO multipods are successfully synthesized on functional substrates using the vapor transport method in a quartz tube. The functional surfaces, which include two different distributions of Ag nanoparticles and a layer of commercial Ag nanowires, are coated onto silicon substrates before the growth of ZnO nanostructures. The structures and morphologies of the ZnO/Ag heterostructures are investigated using X-ray diffraction and field emission scanning electron microscopy. The sizes and shapes of the Ag particles affect the growth rates and initial nucleations of the ZnO structures, resulting in different numbers and shapes of multipods. They also influence the orientation and growth quality of the rods. The optical properties are studied by photoluminescence, UV-vis, and Raman spectroscopy. The results indicate that the surface plasmon resonance strongly depends on the sizes and shapes of the Ag particles.

  14. Direct detection of Pb in urine and Cd, Pb, Cu, and Ag in natural waters using electrochemical sensors immobilized with DMSA functionalized magnetic nanoparticles

    SciTech Connect

    Yantasee, Wassana; Hongsirikarn, Kitiya; Warner, Cynthia L.; Choi, Daiwon; Sangvanich, Thanapon; Toloczko, Mychailo B.; Warner, Marvin G.; Fryxell, Glen E.; Addleman, Raymond S.; Timchalk, Chuck

    2008-03-01

    Urine is universally recognized as one of the best non-invasive matrices for biomonitoring exposure to a broad range of xenobiotics including toxic metals. For direct, simple, and field-deployable monitoring of urinary Pb, electrochemical sensors employing superparamagnetic iron oxide (Fe3O4) nanoparticles with a surface functionalization of dimercaptosuccinic acid (DMSA) has been developed. The metal detection involves rapid collection of dispersed metal-bound nanoparticles from a sample solution at a magnetic or electromagnetic electrode, followed by the stripping voltammetry of the metal in acidic medium. The sensors were evaluated as a function of solution pH, the binding affinity of Pb to DMSA-Fe3O4, the ratio of nanoparticles per sample volume, preconcentration time, and Pb concentrations. The effect of binding competitions between the DMSA-Fe3O4 and urine constituents for Pb on the sensor responses was studied. After 90s of preconcentration in samples containing 25 vol.% of rat urine and 0.1 g/L of DMSA-Fe3O4, the sensor could detect background level of Pb (< 1 ppb) and yielded linear responses from 0 to 50 ppb of Pb, excellent reproducibility (%R.S.D of 5.3 for seven measurements of 30 ppb Pb), and Pb concentrations comparable to those measured by ICP-MS. The sensor could also simultaneously detect background levels (< 1 ppb) of Cd, Pb, Cu, and Ag in river and seawater.

  15. ZnO/Ag/CdO nanocomposite for visible light-induced photocatalytic degradation of industrial textile effluents.

    PubMed

    Saravanan, R; Mansoob Khan, M; Gupta, Vinod Kumar; Mosquera, E; Gracia, F; Narayanan, V; Stephen, A

    2015-08-15

    A ternary ZnO/Ag/CdO nanocomposite was synthesized using thermal decomposition method. The resulting nanocomposite was characterized by X-ray diffraction, field emission scanning electron microscopy, transmission electron microscopy, UV-Vis spectroscopy, and X-ray photoelectron spectroscopy. The ZnO/Ag/CdO nanocomposite exhibited enhanced photocatalytic activity under visible light irradiation for the degradation of methyl orange and methylene blue compared with binary ZnO/Ag and ZnO/CdO nanocomposites. The ZnO/Ag/CdO nanocomposite was also used for the degradation of the industrial textile effluent (real sample analysis) and degraded more than 90% in 210 min under visible light irradiation. The small size, high surface area and synergistic effect in the ZnO/Ag/CdO nanocomposite is responsible for high photocatalytic activity. These results also showed that the Ag nanoparticles induced visible light activity and facilitated efficient charge separation in the ZnO/Ag/CdO nanocomposite, thereby improving the photocatalytic performance.

  16. Thermodynamics of Pb(ii) and Zn(ii) binding to MT-3, a neurologically important metallothionein.

    PubMed

    Carpenter, M C; Shami Shah, A; DeSilva, S; Gleaton, A; Su, A; Goundie, B; Croteau, M L; Stevenson, M J; Wilcox, D E; Austin, R N

    2016-06-01

    Isothermal titration calorimetry (ITC) was used to quantify the thermodynamics of Pb(2+) and Zn(2+) binding to metallothionein-3 (MT-3). Pb(2+) binds to zinc-replete Zn7MT-3 displacing each zinc ion with a similar change in free energy (ΔG) and enthalpy (ΔH). EDTA chelation measurements of Zn7MT-3 and Pb7MT-3 reveal that both metal ions are extracted in a tri-phasic process, indicating that they bind to the protein in three populations with different binding thermodynamics. Metal binding is entropically favoured, with an enthalpic penalty that reflects the enthalpic cost of cysteine deprotonation accompanying thiolate ligation of the metal ions. These data indicate that Pb(2+) binding to both apo MT-3 and Zn7MT-3 is thermodynamically favourable, and implicate MT-3 in neuronal lead biochemistry. PMID:26757944

  17. EDTA and citric acid mediated phytoextraction of Zn, Cu, Pb and Cd through marigold (Tagetes erecta).

    PubMed

    Sinhal, V K; Srivastava, Alok; Singh, V P

    2010-05-01

    Phytoextraction is an emerging cost-effective solution for remediation of contaminated soils which involves the removal of toxins, especially heavy metals and metalloids, by the roots of the plants with subsequent transport to aerial plant organs. The aim of the present investigation is to study the effects of EDTA and citric acid on accumulation potential of marigold (Tagetes erecta) to Zn, Cu, Pb, and Cd and also to evaluate the impacts of these chelators (EDTA and citric acid) in combination with all the four heavy metals on the growth of marigold. The plants were grown in pots and treated with Zn (7.3 mg l(-1)), Cu (7.5 mg I(-1)), Pb (3.7 mg l(-1)) and Cd (0.2 mg l(-1)) alone and in combination with different doses of EDTA i.e., 10, 20 and 30 mg l(-1). All the three doses of EDTA i.e., 10, 20 and 30 mg l(-1) significantly increased the accumulation of Zn, Cu, Pb and Cd by roots, stems and leaves as compared to control treatments. The 30 mg l(-1) concentration of citric acid showed reduced accumulation of these metals by root, stem and leaves as compared to lower doses i.e., 10 and 20 mg l(-1). Among the four heavy metals, Zn accumulated in the great amount (526.34 mg kg(-1) DW) followed by Cu (443.14 mg kg(-1) DW), Pb (393.16 mg kg(-1) DW) and Cd (333.62 mg kg(-1) DW) in leaves with 30 mg l(-1) EDTA treatment. The highest concentration of EDTA and citric acid (30 mg l(-1)) caused significant reduction in growth of marigold in terms of plant height, fresh weight of plant, total chlorophyll, carbohydrate content and protein content. Thus EDTA and citric acid efficiently increased the phytoextractability of marigold which can be used to remediate the soil contaminated with these metals.

  18. Palaeomagnetism of the Howards Pass Zn-Pb deposits, Yukon, Canada

    NASA Astrophysics Data System (ADS)

    Kawasaki, K.; Symons, D. T. A.

    2012-07-01

    The Howards Pass district is located in the Selwyn Basin, Yukon. The district consists of >15 laminated clastic-dominated (CD) sphalerite-galena (Zn-Pb) deposits in the 'zinc corridor' that trends northwest-southeast and extends for ˜35 km. The stratiform mineralized zone, the Active Member, is hosted in carbonaceous cherts and black shales of the Early Silurian Road River Group. Using mostly thermal and then alternating field step demagnetization isolated a stable characteristic remanent magnetization (ChRM) by the core-magnetization-angle method from 18 sites (339 specimens) in 18 variably oriented exploration drill hole cores from 6 Zn-Pb mineralized panels. Rock magnetic analyses show that the main remanence carriers are single- or pseudosingle-domain pyrrhotite and titanomagnetite. The deposits' mean ChRM direction yields a pole position of either ˜170 Ma on the North American apparent polar wander path or ˜162 Ma on a corrected path for the Intermontane Belt (IMB) terranes. A negative palaeomagnetic fold test indicates that the mineralization's ChRM is post-folding, setting a minimum age for regional metamorphic deformation of ˜170 ± 20 Ma and supporting an Early Jurassic arrival for the IMB's collision and accretion to North America. An autochthonous or para-autochthonous North American tectonic model is favoured for the ChRM of the metamorphosed Selwyn Basin strata rather than an allochthonous IMB model. Further, the palaeomagnetic age indicates that the coarse-grained Zn-Pb mineralization in fine fractures that cut the laminated fine-grained Zn-Pb mineralization at Howards Pass at least was formed by remobilization during Middle Jurassic metamorphism.

  19. Li and Ag Co-Doped ZnO Photocatalyst for Degradation of RO 4 Dye Under Solar Light Irradiation.

    PubMed

    Dhatshanamurthi, P; Shanthi, M

    2016-06-01

    The synthesis of Li doped Ag-ZnO (Li-Ag-ZnO) has been successfully achieved by a sonochemically assisted precipitation-decomposition method. The synthesized catalyst was characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), field emission scanning electron microscopy (FE-SEM), energy dispersive spectroscopy (EDS), diffuse reflectance spectra (DRS), photoluminescence spectra (PL), X-ray photoelectron spectra (XPS) and BET surface area measurements. The photocatalytic activity of Li-Ag-ZnO was investigated for the degradation of Reactive orange 4 (RO 4) dye in aqueous solution under solar light irradiation. Co-dopants shift the absorbance of ZnO to the visible region. Li-Ag-ZnO is found to be more efficient than Ag-ZnO, Li-ZnO, commercial ZnO and prepared ZnO at pH 7 for the mineralization of RO 4 dye under solar light irradiation. The influences of operational parameters such as the amount of photocatalyst, dye concentration, initial pH on photo-mineralization of RO 4 have been analyzed. The mineralization of RO 4 dye has been confirmed by COD measurements. A degradation mechanism is proposed for the degradation of RO 4 under solar light. The catalyst was found to be more stable and reusable. PMID:27427652

  20. Spectroscopy study of Zn, Cd, Pb and Cr ions immobilization on C-S-H phase.

    PubMed

    Żak, Renata; Deja, Jan

    2015-01-01

    Calcium silicate hydrates (C-S-H) have a large number of structural sites available for cations and anions to bind. The C-S-H phases are materials which have ability to toxic ions immobilization. Immobilization mechanisms for C-S-H include sorption, phase mixing, substitution and precipitation of insoluble compounds. This study presents the C-S-H (prepared with C/S ratios 1.0) phase as absorbent for immobilization of Zn, Cd, Pb and Cr ions. The C-S-H spectra before and after incorporation of heavy metals ions into the C-S-H structure were obtained. The effect of added heavy metals ions on the hydration phenomena was studied by means of X-ray diffractions analysis. FTIR spectra was measured. The microstructure and phase composition of C-S-H indicate that they can play an essential role in the immobilization of heavy metals. The properties of C-S-H in the presence of Zn, Cd, Pb and Cr cations were studied. The leaching ML test was used to evaluate the level of immobilization of heavy metals in C-S-H. The leached solutions are diluted and analyzed using atomic absorption spectrometry (AAS) and the activated solid particles are separated, washed, desiccated and analyzed by Fourier transform infrared (FTIR) spectroscopy. It was found that the degree of Cd, Zn, Pb and Cr cations immobilization was very high (exceeding 99.96%).

  1. Fractal structures in two-metal electrodeposition systems I: Pb and Zn

    SciTech Connect

    Nakouzi, Elias; Sultan, Rabih

    2011-12-15

    Pattern formation in two-metal electrochemical deposition has been scarcely explored in the chemical literature. In this paper, we report new experiments on zinc-lead fractal co-deposition. Electrodeposits are grown in special cells at a fixed large value of the zinc ion concentration, while that of the lead ion is increased gradually. A very wide diversity of morphologies are obtained and classified. Most of the deposited domains are almost exclusively Pb or Zn. But certain regions originating at the base cathode, ranging from a short grass alley to dense, grown-up bushes or shrubs, manifest a combined Pb-Zn composition. Composition is determined using scanning electron microscopy/energy dispersive x ray measurements as well atomic absorption spectroscopy. Pb domains are characterized by shiny leaf-like and dense deposits as well as flowers with round, balloon-like corollas. The Zn zones display a greater variety of morphologies such as thick trunks and thin and fine branching, in addition to minute ''cigar flower'' structures. The various morphologies are analyzed and classified from the viewpoint of fractal nature, characterized by the box-count fractal dimension. Finally, macroscopic spatial alternation between two different characteristic morphologies is observed under certain conditions.

  2. Determination of Zn, Pb, Cu, and Hg in soils of Ekpan, Nigeria

    SciTech Connect

    Omgbu, J.A.; Kokogho, M.A. )

    1993-01-01

    The concentrations of zinc, lead, copper, and mercury in solids in Ekpan were determined in order to assess the impact of petroleum-refining activities. Twenty soil samples were collected 100 m apart (10 topsoils 0 to 15 cm and 10 bottom soils 15 to 30 cm). Sample solutions prepared were analyzed using the atomic absorption spectrophotometry technique. Results show that top-soil samples contain as much as 7.13 to 13.10 [mu]g/g Zn, 55.13 to 65.50 [mu]g/g Pb, 3.47 to 5.27 [mu]g/g Cu, and 4.00 to 6.50 [mu]g.g Hg. Bottom soil samples contain as much as 7.17 to 13.77 [mu]g/g Zn, 54.97 to 63.23 [mu]g/g Pb, 3.57 to 6.50 [mu]/g Cu, and 4.57 to 6.63 [mu]g/g Hg. The levels reported had an abundance ratio in the order Pb > Zn > Hg > Cu in the soil samples. It is recommended that appropriate measures be put in place by the companies to treat waste effluent before discharging them to the immediate environment. 8 refs., 2 tabs.

  3. Li-Zn-Pb multi isotopic characterization of the Loire River Basin, France

    NASA Astrophysics Data System (ADS)

    Millot, R.; Desaulty, A.; Widory, D.; Bourrain, X.

    2013-12-01

    The Loire River in France is approximately 1010 km long and drains an area of 117 800 km2. Upstream, the Loire River flows following a south to north direction from the Massif Central down to the city of Orléans, 650 km from its source. The Loire River is one of the main European riverine inputs to the Atlantic Ocean. Over time, its basin has been exposed to numerous sources of anthropogenic metal pollutions, such as metal mining, industry, agriculture and domestic inputs. The Loire River basin is thus an excellent study site to develop new isotope systematics for tracking anthropogenic sources of metal pollutions (Zn and Pb) and also to investigate Li isotope tracing that can provide key information on the nature of weathering processes at the Loire River Basin scale. Preliminary data show that Li-Zn-Pb concentrations and isotopic compositions span a wide range in river waters of the Loire River main stream and the main tributaries. There is a clear contrast between the headwaters upstream and rivers located downstream in the lowlands. In addition, one of the major tributaries within the Massif Central (the Allier River) is clearly influenced by inputs resulting from mineralizations and thermomineral waters. The results showed that, on their own, each of these isotope systematics reveals important information about the geogenic or anthropogenic origin Li-Zn-Pb. Considered together, they are however providing a more integrated understanding of the overall budgets of these elements at the scale of the Loire River Basin.

  4. The accumulation of elements in plants growing spontaneously on small heaps left by the historical Zn-Pb ore mining.

    PubMed

    Stefanowicz, Anna M; Stanek, Małgorzata; Woch, Marcin W; Kapusta, Paweł

    2016-04-01

    The study evaluated the levels of nine metals, namely Ca, Cd, Fe, K, Mg, Mn, Pb, Tl, and Zn, in soils and tissues of ten plant species growing spontaneously on heaps left by historical mining for Zn-Pb ores. The concentrations of Cd, Pb, Tl, and Zn in heap soils were much higher than in control soils. Plants growing on heaps accumulated excessive amounts of these elements in tissues, on average 1.3-52 mg Cd kg(-1), 9.4-254 mg Pb kg(-1), 0.06-23 mg Tl kg(-1) and 134-1479 mg Zn kg(-1) in comparison to 0.5-1.1 mg Cd kg(-1), 2.1-11 mg Pb kg(-1), 0.02-0.06 mg Tl kg(-1), and 23-124 mg Zn kg(-1) in control plants. The highest concentrations of Cd, Pb, and Zn were found in the roots of Euphorbia cyparissias, Fragaria vesca, and Potentilla arenaria, and Tl in Plantago lanceolata. Many species growing on heaps were enriched in K and Mg, and depleted in Ca, Fe, and Mn. The concentrations of all elements in plant tissues were dependent on species, organ (root vs. shoot), and species-organ interactions. Average concentrations of Ca, K, and Mg were generally higher in shoots than in roots or similar in the two organs, whereas Cd, Fe, Pb, Tl, and Zn were accumulated predominantly in the roots. Our results imply that heaps left by historical mining for Zn-Pb ores may pose a potential threat to the environment and human health. PMID:26635220

  5. Fast evolution of tropospheric Pb- and Zn-rich particles in the vicinity of a lead smelter

    NASA Astrophysics Data System (ADS)

    Choël, M.; Deboudt, K.; Flament, P.; Lecornet, G.; Perdrix, E.; Sobanska, S.

    Dusts collected on air filters at a Pb-Zn refinery located in northern France were sampled in 1997, 1999 and 2002. The low temporal variability in major elements (Pb, Zn and S) abundances suggested chemical composition of particulate emissions was stable over time. In July 2001 and March 2002, atmospheric aerosols were sampled in the vicinity of the Pb-Zn refinery upwind and downwind from the smelters. Bulk concentrations of major elements (Al, Fe, Pb and Zn) and hydrosoluble ions (Na +, NH 4+, Mg 2+, K +, Ca 2+, Cl - NO 3- and SO 42-) were, respectively, determined by atomic absorption spectrometry and ion chromatography. Elemental and molecular individual particle analyses were, respectively, performed by automated SEM-EDX and Raman microspectrometry. Continental air masses (campaign 2001) were characterized by low Na + and high SO 42-, NO 3- and NH 4+ contents upwind from the smelters. Individual particle analysis of Pb- and Zn-rich airborne particles collected downwind from the refinery indicated elemental associations and molecular speciation were similar to those obtained at the emission: Pb compounds were mainly identified as oxides, sulfates and oxy-sulfates whereas Zn compounds were identified as sulfides. Marine air masses (campaign 2002) were characterized by high Na + contents upwind from the smelters. Individual particle analysis of Pb- and Zn-rich particles collected downwind from the refinery pointed out a systematic association with Na, not emitted by the refinery, suggesting internal mixing of marine aerosols with heavy-metals dusts emitted by the refinery. Such fast evolution of airborne particles chemical composition in the vicinity of the refinery was further proven by SEM-EDX and Raman microspectrometry mappings showing physical evolution by aggregation or coagulation of Zn- and Pb-rich particles with aged sea-salts.

  6. Valorization of biosorbent obtained from a forestry waste: Competitive adsorption, desorption and transport of Cd, Cu, Ni, Pb and Zn.

    PubMed

    Cutillas-Barreiro, Laura; Paradelo, Remigio; Igrexas-Soto, Alba; Núñez-Delgado, Avelino; Fernández-Sanjurjo, María José; Álvarez-Rodriguez, Esperanza; Garrote, Gil; Nóvoa-Muñoz, Juan Carlos; Arias-Estévez, Manuel

    2016-09-01

    Bark from Pinus pinaster is one of the most abundant forestry wastes in Europe, and among the proposed technologies for its reutilization, the removal of heavy metals from wastewater has been gaining increasing attention. In this work, we have studied the performance of pine bark for heavy metal biosorption on competitive systems. Pb, Cu, Ni, Zn and Cd sorption and desorption at equilibrium were studied in batch experiments, whereas transport was studied in column experiments. Batch experiments were performed adding simultaneously different concentrations (0.08-3.15mM) of two or more metals in solution to pine bark samples. Column experiments were performed with 10mM solutions of two metals or a 5mM solution of the five metals. In general, the results under competitive conditions were different to those obtained in monoelemental experiments. The multi-metal batch experiments showed the adsorption sequence Pb≈Cu>Cd>Zn>Ni for lower metal doses, Pb>Cu>Cd>Zn>Ni for intermediate doses, and Pb>Cu>Cd≈Zn≈Ni for high metal doses. Desorption followed the sequence PbPbPb suffered the highest retention, with high capacity to displace Cd, Ni and Zn from adsorption sites on pine bark. The transport experiments produced comparable results to those obtained in the batch experiments, with pine bark retention capacity following the sequence Pb>Cu>Zn>Cd>Ni. The presence of a second metal affected the transport of all the elements studied except Pb, and confirmed the strong influence of Pb and Cu on the retention of the other metals. These results can help to appropriately design decontamination systems using this forestry waste.

  7. Valorization of biosorbent obtained from a forestry waste: Competitive adsorption, desorption and transport of Cd, Cu, Ni, Pb and Zn.

    PubMed

    Cutillas-Barreiro, Laura; Paradelo, Remigio; Igrexas-Soto, Alba; Núñez-Delgado, Avelino; Fernández-Sanjurjo, María José; Álvarez-Rodriguez, Esperanza; Garrote, Gil; Nóvoa-Muñoz, Juan Carlos; Arias-Estévez, Manuel

    2016-09-01

    Bark from Pinus pinaster is one of the most abundant forestry wastes in Europe, and among the proposed technologies for its reutilization, the removal of heavy metals from wastewater has been gaining increasing attention. In this work, we have studied the performance of pine bark for heavy metal biosorption on competitive systems. Pb, Cu, Ni, Zn and Cd sorption and desorption at equilibrium were studied in batch experiments, whereas transport was studied in column experiments. Batch experiments were performed adding simultaneously different concentrations (0.08-3.15mM) of two or more metals in solution to pine bark samples. Column experiments were performed with 10mM solutions of two metals or a 5mM solution of the five metals. In general, the results under competitive conditions were different to those obtained in monoelemental experiments. The multi-metal batch experiments showed the adsorption sequence Pb≈Cu>Cd>Zn>Ni for lower metal doses, Pb>Cu>Cd>Zn>Ni for intermediate doses, and Pb>Cu>Cd≈Zn≈Ni for high metal doses. Desorption followed the sequence PbPbPb suffered the highest retention, with high capacity to displace Cd, Ni and Zn from adsorption sites on pine bark. The transport experiments produced comparable results to those obtained in the batch experiments, with pine bark retention capacity following the sequence Pb>Cu>Zn>Cd>Ni. The presence of a second metal affected the transport of all the elements studied except Pb, and confirmed the strong influence of Pb and Cu on the retention of the other metals. These results can help to appropriately design decontamination systems using this forestry waste. PMID:27232204

  8. Bioaccessibility of Ba, Cu, Pb, and Zn in urban garden and orchard soils.

    PubMed

    Cai, Meifang; McBride, Murray B; Li, Kaiming

    2016-01-01

    Exposure of young children to toxic metals in urban environments is largely due to soil and dust ingestion. Soil particle size distribution and concentrations of toxic metals in different particle sizes are important risk factors in addition to bioaccessibility of these metals in the particles. Analysis of particle size distribution and metals concentrations for 13 soils, 12 sampled from urban gardens and 1 from orchard found that fine particles (<105 μm) comprised from 22 to 66% by weight of the tested soils, with Ba, Cu, Pb and Zn generally at higher concentrations in the finer particles. However, metal bioaccessibility was generally lower in finer particles, a trend most pronounced for Ba and Pb. Gastric was higher than gastrointestinal bioaccessibility for all metals except Cu. The lower bioaccessibility of Pb in urban garden soils compared to orchard soil is attributable to the higher organic matter content of the garden soils. PMID:26477581

  9. Invariant bandwidth of erbium in ZnO-PbO-tellurite glasses: Local probe/model

    SciTech Connect

    Ramamoorthy, Raj Kumar; Bhatnagar, Anil K.

    2014-04-24

    A series of [(70TeO{sub 2}−(30−x)ZnO−xPbO){sub 0.99}−(Er{sub 2}O{sub 3}){sub 0.01}; where x = 5, 10, 15 and 20] tellurite glasses, were prepared using the melt quenching technique. Crucial emission bandwidth of erbium at 1.5 μm has been derived and found to be the same for all the glasses, irrespective of PbO content. This identical bandwidth in all tellurite glasses is attributed to the presence of erbium in tellurium rich disordered environments. This result has been complemented through XANES spectra and the obtained invariant first shell of 6.5 oxygen atoms, confirm the unchanged environment in these glasses for all PbO content.

  10. Photosensitization of ZnO Crystals with Iodide-Capped PbSe Quantum Dots.

    PubMed

    King, Laurie A; Parkinson, B A

    2016-07-21

    Lead selenide (PbSe) quantum dots (QDs) are an attractive material for application in photovoltaic devices due to the ability to tune their band gap, efficient multiple exciton generation, and high extinction coefficients. However, PbSe QDs are quite unstable to oxidation in air. Recently there have been multiple studies detailing postsynthetic halide treatments to stabilize lead chalcogenide QDs. We exploit iodide-stabilized PbSe QDs in a model QD-sensitized solar cell configuration where zinc oxide (ZnO) single crystals are sensitized using cysteine as a bifunctional linker molecule. Sensitized photocurrents stable for >1 h can be measured in aqueous KI electrolyte that is usually corrosive to QDs under illumination. The spectral response of the sensitization extended out to 1700 nm, the farthest into the infrared yet observed. Hints of the existence of multiple exciton generation and collection as photocurrent, as would be expected in this system, are speculated and discussed. PMID:27398873

  11. Preparation and use of photocatalytically active segmented Ag|ZnO and coaxial TiO2-Ag nanowires made by templated electrodeposition.

    PubMed

    Maijenburg, A Wouter; Rodijk, Eddy J B; Maas, Michiel G; Ten Elshof, Johan E

    2014-05-02

    Photocatalytically active nanostructures require a large specific surface area with the presence of many catalytically active sites for the oxidation and reduction half reactions, and fast electron (hole) diffusion and charge separation. Nanowires present suitable architectures to meet these requirements. Axially segmented Ag|ZnO and radially segmented (coaxial) TiO2-Ag nanowires with a diameter of 200 nm and a length of 6-20 µm were made by templated electrodeposition within the pores of polycarbonate track-etched (PCTE) or anodized aluminum oxide (AAO) membranes, respectively. In the photocatalytic experiments, the ZnO and TiO2 phases acted as photoanodes, and Ag as cathode. No external circuit is needed to connect both electrodes, which is a key advantage over conventional photo-electrochemical cells. For making segmented Ag|ZnO nanowires, the Ag salt electrolyte was replaced after formation of the Ag segment to form a ZnO segment attached to the Ag segment. For making coaxial TiO2-Ag nanowires, a TiO2 gel was first formed by the electrochemically induced sol-gel method. Drying and thermal annealing of the as-formed TiO2 gel resulted in the formation of crystalline TiO2 nanotubes. A subsequent Ag electrodeposition step inside the TiO2 nanotubes resulted in formation of coaxial TiO2-Ag nanowires. Due to the combination of an n-type semiconductor (ZnO or TiO2) and a metal (Ag) within the same nanowire, a Schottky barrier was created at the interface between the phases. To demonstrate the photocatalytic activity of these nanowires, the Ag|ZnO nanowires were used in a photocatalytic experiment in which H2 gas was detected upon UV illumination of the nanowires dispersed in a methanol/water mixture. After 17 min of illumination, approximately 0.2 vol% H2 gas was detected from a suspension of ~0.1 g of Ag|ZnO nanowires in a 50 ml 80 vol% aqueous methanol solution.

  12. Preparation and Use of Photocatalytically Active Segmented Ag|ZnO and Coaxial TiO2-Ag Nanowires Made by Templated Electrodeposition

    PubMed Central

    Maijenburg, A. Wouter; Rodijk, Eddy J.B.; Maas, Michiel G.; ten Elshof, Johan E.

    2014-01-01

    Photocatalytically active nanostructures require a large specific surface area with the presence of many catalytically active sites for the oxidation and reduction half reactions, and fast electron (hole) diffusion and charge separation. Nanowires present suitable architectures to meet these requirements. Axially segmented Ag|ZnO and radially segmented (coaxial) TiO2-Ag nanowires with a diameter of 200 nm and a length of 6-20 µm were made by templated electrodeposition within the pores of polycarbonate track-etched (PCTE) or anodized aluminum oxide (AAO) membranes, respectively. In the photocatalytic experiments, the ZnO and TiO2 phases acted as photoanodes, and Ag as cathode. No external circuit is needed to connect both electrodes, which is a key advantage over conventional photo-electrochemical cells. For making segmented Ag|ZnO nanowires, the Ag salt electrolyte was replaced after formation of the Ag segment to form a ZnO segment attached to the Ag segment. For making coaxial TiO2-Ag nanowires, a TiO2 gel was first formed by the electrochemically induced sol-gel method. Drying and thermal annealing of the as-formed TiO2 gel resulted in the formation of crystalline TiO2 nanotubes. A subsequent Ag electrodeposition step inside the TiO2 nanotubes resulted in formation of coaxial TiO2-Ag nanowires. Due to the combination of an n-type semiconductor (ZnO or TiO2) and a metal (Ag) within the same nanowire, a Schottky barrier was created at the interface between the phases. To demonstrate the photocatalytic activity of these nanowires, the Ag|ZnO nanowires were used in a photocatalytic experiment in which H2 gas was detected upon UV illumination of the nanowires dispersed in a methanol/water mixture. After 17 min of illumination, approximately 0.2 vol% H2 gas was detected from a suspension of ~0.1 g of Ag|ZnO nanowires in a 50 ml 80 vol% aqueous methanol solution. PMID:24837535

  13. Pb(II)-promoted amide cleavage: mechanistic comparison to a Zn(II) analogue.

    PubMed

    Elton, Eric S; Zhang, Tingting; Prabhakar, Rajeev; Arif, Atta M; Berreau, Lisa M

    2013-10-01

    Two new Pb(II) complexes of the amide-appended nitrogen/sulfur epppa (N-((2-ethylthio)ethyl)-N-((6-pivaloylamido-2-pyridyl)methyl)-N-((2-pyridyl)methyl)amine) chelate ligand, [(epppa)Pb(NO3)2] (4-NO3) and [(epppa)Pb(ClO4)2] (4-ClO4), were prepared and characterized. In the solid state, 4-NO3 exhibits κ(5)-epppa chelate ligand coordination as well as the coordination of two bidentate nitrate ions. In acetonitrile, 4-NO3 is a 1:1 electrolyte with a coordinated NO3(-), whereas 4-ClO4 is a 1:2 electrolyte. Treatment of 4-ClO4 with 1 equiv Me4NOH·5H2O in CH3CN:CH3OH (3:5) results in amide methanolysis in a reaction that is akin to that previously reported for the Zn(II) analogue [(epppa)Zn](ClO4)2 (3-ClO4). (1)H NMR kinetic studies of the amide methanolysis reactions of 4-ClO4 and 3-ClO4 as a function of temperature revealed free energies of activation of 21.3 and 24.5 kcal/mol, respectively. The amide methanolysis reactions of 4-ClO4 and 3-ClO4 differ in terms of the effect of the concentration of methanol (saturation kinetics for 4-ClO4; second-order behavior for 3-ClO4), the observation of a small solvent kinetic isotope effect (SKIE) only for the reaction of the Zn(II)-containing 3-ClO4, and the properties of an initial intermediate isolated from each reaction upon treatment with Me4NOH·5H2O. These experimental results, combined with computational studies of the amide methanolysis reaction pathways of 4-ClO4 and 3-ClO4, indicate that the Zn(II)-containing 3-ClO4 initially undergoes amide deprotonation upon treatment with Me4NOH·5H2O. Subsequent amide protonation from coordinated methanol yields a structure containing a coordinated neutral amide and methoxide anion from which amide cleavage can then proceed. The rate-determining step in this pathway is either amide protonation or protonation of the leaving group. The Pb(II)-containing 4-ClO4 instead directly forms a neutral amide-containing, epppa-ligated Pb(II)-OH/Pb(II)-OCH3 equilibrium mixture upon treatment

  14. The first report of Pb and Zn accumulation in some native plants from the Peruvian Andes

    NASA Astrophysics Data System (ADS)

    Bech, Jaume; Duran, Paola; Poma, Wilfredo; Sánchez, Isidoro; Barceló, Juan; Roca, Núria; Boluda, Rafael; Roca-Pérez, Luís.; Poschenrieder, Charlotte

    2010-05-01

    Until recent decades little has been known about the remediation of mining sites using metalophytes in Latin America. Metal mining has helped to create severe and diverse environmental problems. The present study proposed to identify and characterize spontaneously growing heavy metal tolerant plant species in the area around the polimetalic mine in Hualgayoc (Cajamarca, Peru). These species are potentially useful for phytorremediation. Plant and soils from their rhizosphere were sampled and analized for concentration of As, Fe, Mn, Pb and Zn. Translocation Factor (TF) defined the metals concentrations ratio between shoots and root biomass and Shoot Accumulation Factor (SAF) the metal concentration ratio between shoot and soil concentration were determined and used to measure the effectiveness of a plant in concentrating metals into its biomass. The soils were neutral pH (7,4±0,5) with variable content of organic carbon (2,4±1,1) and loam texture: sand (42,9±10,8) and clay (16,7±4,6). According to the total metals, all samples exceeded toxicity thresholds, high Pb (20016 ± 32559 mg•kg-1) and Zn (22512 ± 13056 mg•kg-1) concentrations were detected. High shoot Pb and Zn concentrations were found in Plantaginaceae Plantago orbignyana (6998 and 9617 μg/g); Brassicaceae Lepidium bipinnatifidum (6886 and 5034 mg•kg-1) and Asteraceae Senecio sp (4253 and 3870 mg•kg-1) and Baccharis latifolia (2554 and 1284 mg•kg-1 respectively). The high values of TFs indicates that the plants effectively traslocated metales. Lepidium bipinnatifidum shows the highest TFs values (143 in Pb and 21,5 in Zn). The SAF values were much lower than those reported for other species such as Paspalum sp in the Peruvian copper mine, which may be due to a high top soil Pb and Zn concentrations. These species can surely be considered as interesting for phytoextraction, due not only to its accumulative capacity but also since they showed an elevated transfer factor and grew in the

  15. Bandgap and Structure Engineering via Cation Exchange: From Binary Ag2S to Ternary AgInS2, Quaternary AgZnInS alloy and AgZnInS/ZnS Core/Shell Fluorescent Nanocrystals for Bioimaging.

    PubMed

    Song, Jiangluqi; Ma, Chao; Zhang, Wenzhe; Li, Xiaodong; Zhang, Wenting; Wu, Rongbo; Cheng, Xiangcan; Ali, Asad; Yang, Mingya; Zhu, Lixin; Xia, Ruixiang; Xu, Xiaoliang

    2016-09-21

    Attention on semiconductor nanocrystals have been largely focused because of their unique optical and electrical properties, which can be applied as light absorber and luminophore. However, the band gap and structure engineering of nanomaterials is not so easy because of their finite size. Here we demonstrate an approach for preparing ternary AgInS2 (AIS), quaternary AgZnInS (AZIS), AgInS2/ZnS and AgZnInS/ZnS nanocompounds based on cation exchange. First, pristine Ag2S quantum dots (QDs) with different sizes were synthesized in one-pot, followed by the partial cation exchange between In(3+) and Ag(+). Changing the initial ratio of In(3+) to Ag(+), reaction time and temperature can control the components of the obtained AIS QDs. Under the optimized conditions, AIS QDs were obtained for the first time with a cation disordered cubic phase and high photoluminescence (PL) quantum yield (QY) up to 32% in aqueous solution, demonstrating the great potential of cation exchange in the synthesis for nanocrystals with excellent optical properties. Sequentially, Zn(2+) ions were incorporated in situ through a second exchange of Zn(2+) to Ag(+)/In(3+), leading to distinct results under different reaction temperature. Addition of Zn(2+) precursor at room temperature produced AIS/ZnS core/shell NCs with successively enhancement of QY, while subsequent heating could obtain AZIS homogeneous alloy QDs with a successively blue-shift of PL emission. This allow us to tune the PL emission of the products from 483 to 675 nm and fabricate the chemically stable QDs core/ZnS shell structure. Based on the above results, a mechanism about the cation exchange for the ternary nanocrystals of different structures was proposed that the balance between cation exchange and diffusion is the key factor of controlling the band gap and structure of the final products. Furthermore, photostability and in vitro experiment demonstrated quite low cytotoxicity and remarkably promising applications in the

  16. Bandgap and Structure Engineering via Cation Exchange: From Binary Ag2S to Ternary AgInS2, Quaternary AgZnInS alloy and AgZnInS/ZnS Core/Shell Fluorescent Nanocrystals for Bioimaging.

    PubMed

    Song, Jiangluqi; Ma, Chao; Zhang, Wenzhe; Li, Xiaodong; Zhang, Wenting; Wu, Rongbo; Cheng, Xiangcan; Ali, Asad; Yang, Mingya; Zhu, Lixin; Xia, Ruixiang; Xu, Xiaoliang

    2016-09-21

    Attention on semiconductor nanocrystals have been largely focused because of their unique optical and electrical properties, which can be applied as light absorber and luminophore. However, the band gap and structure engineering of nanomaterials is not so easy because of their finite size. Here we demonstrate an approach for preparing ternary AgInS2 (AIS), quaternary AgZnInS (AZIS), AgInS2/ZnS and AgZnInS/ZnS nanocompounds based on cation exchange. First, pristine Ag2S quantum dots (QDs) with different sizes were synthesized in one-pot, followed by the partial cation exchange between In(3+) and Ag(+). Changing the initial ratio of In(3+) to Ag(+), reaction time and temperature can control the components of the obtained AIS QDs. Under the optimized conditions, AIS QDs were obtained for the first time with a cation disordered cubic phase and high photoluminescence (PL) quantum yield (QY) up to 32% in aqueous solution, demonstrating the great potential of cation exchange in the synthesis for nanocrystals with excellent optical properties. Sequentially, Zn(2+) ions were incorporated in situ through a second exchange of Zn(2+) to Ag(+)/In(3+), leading to distinct results under different reaction temperature. Addition of Zn(2+) precursor at room temperature produced AIS/ZnS core/shell NCs with successively enhancement of QY, while subsequent heating could obtain AZIS homogeneous alloy QDs with a successively blue-shift of PL emission. This allow us to tune the PL emission of the products from 483 to 675 nm and fabricate the chemically stable QDs core/ZnS shell structure. Based on the above results, a mechanism about the cation exchange for the ternary nanocrystals of different structures was proposed that the balance between cation exchange and diffusion is the key factor of controlling the band gap and structure of the final products. Furthermore, photostability and in vitro experiment demonstrated quite low cytotoxicity and remarkably promising applications in the

  17. Concentrations, spatial distribution, and risk assessment of soil heavy metals in a Zn-Pb mine district in southern China.

    PubMed

    Qi, Jianying; Zhang, Hailong; Li, Xiangping; Lu, Jian; Zhang, Gaosheng

    2016-07-01

    China is one of the largest producers and consumers of lead and zinc in the world. Lead and zinc mining and smelting can release hazardous heavy metals such as Cd, Pb, Zn, and As into soils, exerting health risks to human by chronic exposure. The concentrations of Cd, Zn, Pb, and As in soil samples collected from a Pb-Zn mining area with exploitation history of 60 years were investigated. Health risks of the heavy metals in soil were evaluated using US Environmental Protection Agency (US EPA) recommended method. A geo-statistical technique (Kriging) was used for the interpolation of heavy metals pollution and Hazard Index (HI). The results indicated that the long-term Pb/Zn mining activities caused the serious pollution in the local soil. The concentrations of Cd, As, Pb, and Zn in topsoil were 40.3 ± 6.3, 103.7 ± 37.3, 3518.4 ± 896.1, and 10,413 ± 2973.2 mg/kg dry weight, respectively. The spatial distribution of the four metals possessed similar patterns, with higher concentrations around Aayiken (AYK), Maseka (MSK), and Kuangshan (KS) area and more rapidly dropped concentrations at upwind direction than those at downwind direction. The main pollutions of Cd and Zn were found in the upper 60 cm, the Pb was found in the upper 40 cm, and the As was in the upper 20 cm. The mobility of metals in soil profile of study area was classed as Cd > Zn ≫ Pb > As. Results indicated that there was a higher health risk (child higher than adult) in the study area. Pb contributed to the highest Hazard Quotient (57.0 ~ 73.9 %) for the Hazard Index. PMID:27315126

  18. Concentrations, spatial distribution, and risk assessment of soil heavy metals in a Zn-Pb mine district in southern China.

    PubMed

    Qi, Jianying; Zhang, Hailong; Li, Xiangping; Lu, Jian; Zhang, Gaosheng

    2016-07-01

    China is one of the largest producers and consumers of lead and zinc in the world. Lead and zinc mining and smelting can release hazardous heavy metals such as Cd, Pb, Zn, and As into soils, exerting health risks to human by chronic exposure. The concentrations of Cd, Zn, Pb, and As in soil samples collected from a Pb-Zn mining area with exploitation history of 60 years were investigated. Health risks of the heavy metals in soil were evaluated using US Environmental Protection Agency (US EPA) recommended method. A geo-statistical technique (Kriging) was used for the interpolation of heavy metals pollution and Hazard Index (HI). The results indicated that the long-term Pb/Zn mining activities caused the serious pollution in the local soil. The concentrations of Cd, As, Pb, and Zn in topsoil were 40.3 ± 6.3, 103.7 ± 37.3, 3518.4 ± 896.1, and 10,413 ± 2973.2 mg/kg dry weight, respectively. The spatial distribution of the four metals possessed similar patterns, with higher concentrations around Aayiken (AYK), Maseka (MSK), and Kuangshan (KS) area and more rapidly dropped concentrations at upwind direction than those at downwind direction. The main pollutions of Cd and Zn were found in the upper 60 cm, the Pb was found in the upper 40 cm, and the As was in the upper 20 cm. The mobility of metals in soil profile of study area was classed as Cd > Zn ≫ Pb > As. Results indicated that there was a higher health risk (child higher than adult) in the study area. Pb contributed to the highest Hazard Quotient (57.0 ~ 73.9 %) for the Hazard Index.

  19. Growth of high performance piezoelectric crystal Pb(Zn1/3Nb2/3)O3-PbTiO3 using PbO flux.

    PubMed

    Jin, Min; Xu, Jiayue; Shi, Minli; Wu, Xianjun; Tong, Jian

    2007-05-01

    Novel piezoelectric crystal (1-x)Pb(Zn(1/3)Nb(2/3))O(3)-xPbTiO(3) (PZNT) has attracted much attention due to its high piezoelectric properties and potential applications in medical ultrasonic devices, sonar transducers, solid state actuators. However, the applications of PZNT crystals are limited by the lack of a simple and reproducible growth technique. In this work, large size PZNT crystals were grown by the vertical Bridgman method using 50 mol% PbO as a flux. The growth conditions were optimized as mole ratio of raw materials and flux=1:1, soaking temperature 1150-1200 degrees C, soaking time 10 h, the lowering rate of the crucible 0.5 mm/h and the temperature gradient near solid-liquid interface about 50 degrees C/mm. The maximum size of as-grown PZNT crystal was about 60 mm in length. The crystal was oriented and its piezoelectric constant d(33) and coupling coefficient k(33) were measured over 2000pC/N and 0.92, respectively.

  20. Tracing Cd, Zn and Pb pollution sources in bivalves using isotopes

    NASA Astrophysics Data System (ADS)

    Shiel, A. E.; Weis, D. A.; Orians, K. J.

    2010-12-01

    In a multi-tracer study, Cd, Zn and Pb isotopes (MC-ICP-MS) and elemental concentrations (HR-ICP-MS) are evaluated as tools to distinguish between natural and anthropogenic sources of these metals in bivalves from western Canada (British Columbia), the eastern USA, Hawaii and France. High Cd concentrations found in BC oysters have elicited economic and health concerns. The source of these high Cd levels is unknown but thought to be largely natural. High Cd levels in BC oysters are largely attributed to the natural upwelling of Cd-rich intermediate waters in the North Pacific as the δ114/110Cd (-0.69 to -0.09‰) and δ66/64Zn (0.28 to 0.36‰) values of BC oysters fall within the range reported for North Pacific seawater. Different contributions from anthropogenic sources account for the variability of Cd isotopic compositions of BC oysters; the lightest of these oysters are from the BC mainland. These oysters also have Pb isotopic compositions that reflect primarily anthropogenic sources (e.g., leaded and unleaded automotive gasoline and smelting of Pb ores, potentially historical). On the contrary, USA East Coast bivalves exhibit relatively light Cd isotopic compositions (δ114/110Cd = -1.20 to -0.54‰; lighter than reported for North Atlantic seawater) due to the high prevalence of industry on this coast. The Pb isotopic compositions of these bivalves indicate contributions from the combustion of coal. The large variability of environmental health among coastal areas in France is reflected in the broad range of Cd isotopic compositions exhibited by French bivalves (δ114/110Cd = -1.08 to -0.20‰). Oysters and mussels from the Marennes-Oléron basin and Gironde estuary have the lightest Cd isotopic compositions of the French oysters consistent with significant historical Cd emissions from the now-closed proximal Zn smelter. In these bivalves, significant declines in the Cd levels between 1984/7 and 2004/5 are not accompanied by a significant shift in the Cd

  1. Comparative modular analysis of two complex sulfosalt structures: sterryite, Cu(Ag,Cu)3Pb19(Sb,As)22(As-As)S56, and parasterryite, Ag4Pb20(Sb,As)24S58.

    PubMed

    Moëlo, Yves; Guillot-Deudon, Catherine; Evain, Michel; Orlandi, Paolo; Biagioni, Cristian

    2012-10-01

    The crystal structures of two very close, but distinct complex minerals of the lead sulfosalt group have been solved: sterryite, Cu(Ag,Cu)(3)Pb(19)(Sb,As)(22)(As-As)S(56), and parasterryite, Ag(4)Pb(20)(Sb,As)(24)S(58). They are analyzed and compared according to modular analysis. The fundamental building block is a complex column centred on a Pb(6)S(12) triangular prismatic core, with two additional long and short arms. The main chemical and topological differences relate to the short arm, which induces a relative a/4 shift (~2 Å along the elongation parameter) of the constitutive rod layers, as illustrated by distinct cell settings within the same space group (P2(1)/n and P2(1)/c, respectively). Selection of the shortest (i.e. strongest) (Sb,As)-S bonds permitted to enhance the polymeric organization of (Sb,As) atoms with triangular pyramidal coordination. These two quasi-homeotypic structures are expanded derivatives of owyheeite, Ag(3)Pb(10)Sb(11)S(28). The hierarchy of organization levels from zero- to three-dimensional entities is subordinated to building operators, which appear as the driving force for the construction of such complex structures. Minor cations (Ag, Cu) or the As-As pair in sterryite secure the final locking, which favours the formation of one or the other compound. PMID:22992793

  2. Spectral analysis of Cu(2+): B(2)O(3)--ZnO--PbO glasses.

    PubMed

    Lakshminarayana, G; Buddhudu, S

    2005-11-01

    A new series of heavy metal oxide (PbO) based zinc borate glasses in the chemical composition of (95-x)B(2)O(3)-5ZnO-xPbO (x=10, 15, 20, 25, 30, 35, 40, 45 and 50 mol%) have been prepared to verify their UV filtering performance. Both direct and indirect optical band gaps (E(opt)) have been evaluated for these glasses. For a reference glass of 45B(2)O(3)-5ZnO-50PbO, refractive indices at different wavelengths are measured and found the results satisfactorily correlated with the theoretical data upon the computation of Cauchy's constants of A=1.766029949, B=159531.024 nm(2) and C=-1.078 x 10(10) nm(4). Measurements concerning X-ray diffraction (XRD), FT-IR, differential scanning colorimeter (DSC) profiles have been carried out for this glass. The FT-IR profile has revealed that the glass has both BO(3) and BO(4) units. From DSC thermogram, glass transition temperature (T(g)), crystallization temperature (T(c)) and melting temperature (T(m)) have been located and from them, other related parameters of the glass have also been calculated. Visible absorption spectra of 45B(2)O(3)-5ZnO-(50-x)PbO-xCuO (x=0. 1, 0.2, 0.5 and 1.0 mol%) have revealed two absorption bands at around 400 nm ((2)B(1g)-->(2)E(g)) and 780 nm ((2)B(1g)-->(2)B(2g)) of Cu(2+) ions, respectively. Emission bands at 422 and 512 nm are found for the 1 mol % CuO doped glass with excitations at 306 and 332 nm.

  3. The structure, morphology, and the metal-enhanced fluorescence of nano-Ag/ZnO core-shell structure

    NASA Astrophysics Data System (ADS)

    Zhao, Yue; Ding, Yanli; Peng, Xiang; Zhou, Mingtao; Liang, Xiaoyan; Min, Jiahua; Wang, Linjun; Shi, Weimin

    2014-09-01

    Nano-polyc rystalline silver (Ag) particles with the diameter of 60 nm were synthesized by the reducing agent sodium citrate. An amorphous zinc oxide (ZnO) shell layer was then coated on the surface of silver particles using wet chemical method. The Ag/ZnO core-shell structure was characterized by scanning electron microscope, transmission electron microscopy, ultraviolet-visible spectroscopy and fluorescence (FL) measurement. The results showed that nano-Ag/ZnO core-shell particles with an average diameter of ~100 nm were prepared successfully, and the FL intensity of Rhodamine 6G (R6G) mixed with Ag/ZnO nanoparticle was 53 % greater than that of the same amount of R6G without any nanoparticles, which may be related to the effect of surface plasmon resonance.

  4. The structure, morphology, and the metal-enhanced fluorescence of nano-Ag/ZnO core-shell structure

    NASA Astrophysics Data System (ADS)

    Zhao, Yue; Ding, Yanli; Peng, Xiang; Zhou, Mingtao; Liang, Xiaoyan; Min, Jiahua; Wang, Linjun; Shi, Weimin

    2015-06-01

    Nano-polyc rystalline silver (Ag) particles with the diameter of 60 nm were synthesized by the reducing agent sodium citrate. An amorphous zinc oxide (ZnO) shell layer was then coated on the surface of silver particles using wet chemical method. The Ag/ZnO core-shell structure was characterized by scanning electron microscope, transmission electron microscopy, ultraviolet-visible spectroscopy and fluorescence (FL) measurement. The results showed that nano-Ag/ZnO core-shell particles with an average diameter of ~100 nm were prepared successfully, and the FL intensity of Rhodamine 6G (R6G) mixed with Ag/ZnO nanoparticle was 53 % greater than that of the same amount of R6G without any nanoparticles, which may be related to the effect of surface plasmon resonance.

  5. Synthesis of Ag-ZnO with multiple rods (multipods) morphology and its application in the simultaneous photo-catalytic degradation of methyl orange and methylene blue.

    PubMed

    Arab Chamjangali, M; Bagherian, G; Javid, A; Boroumand, S; Farzaneh, N

    2015-11-01

    In this study, the photo-decolorization of a mixture of methylene blue (MB) and methyl orange (MO) was investigated using Ag-ZnO multipods. The photo-catalyst used, ZnO multipods, was successfully synthesized. The surface of ZnO microstructure was modified by deposition of different amounts of Ag nanoparticles (Ag NPs) using the photo-reduction method. The as-prepared samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), UV-Vis and atomic absorption spectroscopy. The photo-catalytic efficiency of Ag-ZnO is mainly controlled by the amount of Ag NPs deposited on the ZnO surface. The results obtained suggest that Ag-ZnO containing 6.5% Ag NPs, has the highest photo-catalytic performance in the simultaneous photo-degradation of dyes at a shorter time.

  6. Ore geology and fluid inclusion geochemistry of the Tiemurt Pb-Zn-Cu deposit, Altay, Xinjiang, China: A case study of orogenic-type Pb-Zn systems

    NASA Astrophysics Data System (ADS)

    Zhang, Li; Zheng, Yi; Chen, YanJing

    2012-04-01

    The Tiemurt Pb-Zn-Cu deposit is hosted in a Devonian volcanic-sedimentary basin of the Altay orogenic belt, and is thus interpreted to have formed by sea-floor hydrothermal exhalation in previous studies. Our investigation discovered that the deposit is not stratiform or stratabound, but structure-controlled instead. The hydrothermal ore-forming process can be divided into the early, middle and late stage, represented by pyrite-quartz, polymetallic sulfide-quartz and carbonate-quartz veinlets, respectively. The early-stage veins and contained minerals are structurally deformed and brecciated, suggesting a compressional or transpressional tectonic regime. The middle-stage veinlets intrude and infill the fissures of the early-stage assemblages, and show no deformation, suggesting a tensional shear setting. The late-stage veinlets mostly infill open-space fissures that crosscut veins and replacements formed in the earlier stages. Four types of fluid inclusions (FIs), including aqueous (type W), carbonic-aqueous (type C), pure carbonic (type PC) and solid-bearing (type S), are identified at the Tiemurt deposit. The early-stage minerals contain the C- and W-type primary FIs that are totally homogenized at temperatures of 330-390 °C with low salinities of 0.8-11.9 wt.% NaCl eqv.; whilst the late-stage quartz or calcite contains only the W-type FIs with homogenization temperatures of 118-205 °C, and salinities of 1.4-3.4 wt.% NaCl eqv. This indicates that the ore fluid system evolved from CO2-rich, probably metamorphic to CO2-poor, meteoric fluids; and that a significant CO2-escape must have occurred. All the four types of FIs can be only observed in the middle-stage minerals, and even in a microscopic domain of a crystal, representing an association trapped from a boiling fluid system. These FIs homogenize at temperatures ranging from 270 to 330 °C, with two salinity clusters of 1.9-14.5 and 37.4-42.4 wt.% NaCl eqv., respectively. This implies that metal precipitation

  7. Plasmon-Enhanced Surface Photovoltage of ZnO/Ag Nanogratings

    PubMed Central

    Gwon, Minji; Sohn, Ahrum; Cho, Yunae; Phark, Soo-Hyon; Ko, Jieun; Sang Kim, Youn; Kim, Dong-Wook

    2015-01-01

    We investigated the surface photovoltage (SPV) behaviors of ZnO/Ag one-dimensional (1D) nanogratings using Kelvin probe force microscopy (KPFM). The grating structure could couple surface plasmon polaritons (SPPs) with photons, giving rise to strong light confinement at the ZnO/Ag interface. The larger field produced more photo-excited carriers and increased the SPV. SPP excitation influenced the spatial distribution of the photo-excited carriers and their recombination processes. As a result, the SPV relaxation time clearly depended on the wavelength and polarization of the incident light. All of these results suggested that SPV measurement using KPFM should be very useful for studying the plasmonic effects in nanoscale metal/semiconductor hybrid structures. PMID:26567529

  8. Physiological responses and detoxific mechanisms to Pb, Zn, Cu and Cd in young seedlings of Paulownia fortunei.

    PubMed

    Wang, Jiang; Li, Weihua; Zhang, Chongbang; Ke, Shisheng

    2010-01-01

    Paulownia fortunei has been successfully used in the phytoremediation of many Pb/Zn mine tailings. However, seed germination and young seedlings of P. fortunei rarely occurred in these mine tailings. The physiological responses and detoxific mechanisms of P. fortunei young seedling to Pb, Zn, Cu and Cd stress were investigated. The germinated rate, shoot length, chlorophyll and carotenoid contents in leaves of young seedlings had a great reduction under Zn and Cu treatments, but had little decrease under Pb and Cd treatments. The production rate of O2*-, H2O2 and malondialdehyde (MDA) contents significantly increased in response to added Zn and Cu indicating great oxidative stress for young seedlings, but they had no significant change to added Pb and Cd. Young seedlings had effective detoxific mechanism to Pb and Cd, as antioxidant enzymes activities, phytochelatins (PCs-SH) and proline contents increased with increasing rates of added Pb and Cd. However, young seedlings had un-effective detoxific mechanisms to Zn and Cu stress. Results revealed the heavy metals (such as Cu) that present at low concentrations in mine tailings may be major constraint for the survival of young seedlings. PMID:21462710

  9. Crystalline and quasicrystalline allotropes of Pb formed on the fivefold surface of icosahedral Ag-In-Yb

    SciTech Connect

    Sharma, H. R. Smerdon, J. A.; Nugent, P. J.; Ribeiro, A.; McGrath, R.; McLeod, I.; Dhanak, V. R.; Shimoda, M.; Tsai, A. P.

    2014-05-07

    Crystalline and quasicrystalline allotropes of Pb are formed by evaporation on the fivefold surface of the icosahedral (i) Ag-In-Yb quasicrystal under ultra-high vacuum. Lead grows in three dimensional quasicrystalline order and subsequently forms fivefold-twinned islands with the fcc(111) surface orientation atop of the quasicrystalline Pb. The islands exhibit specific heights (magic heights), possibly due to the confinement of electrons in the islands. We also study the adsorption behavior of C{sub 60} on the two allotropes of Pb. Scanning tunneling microcopy reveals that a high corrugation of the quasicrystalline Pb limits the diffusion of the C{sub 60} molecules and thus produces a disordered film, similar to adsorption behavior of the same molecules on the clean substrate surface. However, the sticking coefficient of C{sub 60} molecules atop the Pb islands approaches zero, regardless of the overall C{sub 60} coverage.

  10. Tuning the properties of ZnO, hematite, and Ag nanoparticles by adjusting the surface charge.

    PubMed

    Zhang, Jianhui; Dong, Guanjun; Thurber, Aaron; Hou, Yayi; Gu, Min; Tenne, Dmitri A; Hanna, C B; Punnoose, Alex

    2012-03-01

    A poly (acryl acid) (PAA) post-treatment method is performed to modify the surface charge of ZnO nanospheres, hematite nanocubes, and Ag nanoprisms from highly positive to very negative by adjusting the PAA concentration, to and greatly modify their photoluminescence, cytotoxicity, magnetism, and surface plasmon resonance. This method provides a general way to tune the nanoparticle properties for broad physicochemical and biological applications. PMID:22298490

  11. Electrokinetic enhancement on phytoremediation in Zn, Pb, Cu and Cd contaminated soil using potato plants.

    PubMed

    Aboughalma, Hanssan; Bi, Ran; Schlaak, Michael

    2008-07-01

    The use of a combination of electrokinetic remediation and phytoremediation to decontaminate soil polluted with heavy metals has been demonstrated in a laboratory-scale experiment. Potato tubers were planted in plastic vessels filled with Zn, Pb, Cu and Cd contaminated soil and grown in a greenhouse. Three of these vessels were treated with direct current electric field (DC), three with alternative current (AC) and three remained untreated as control vessels. The soil pH varied from anode to cathode with a minimum of pH 3 near the anode and a maximum of pH 8 near the cathode in the DC treated soil profile. There was an accumulation of Zn, Cu and Cd at about 12 cm distance from anode when soil pH was 5 in the DC treated soil profile. There was no significant metal redistribution and pH variation between anode and cathode in the AC soil profile. The biomass production of the plants was 72% higher under AC treatment and 27% lower under DC treatment compared to the control. Metal accumulation was generally higher in the plant roots treated with electrical fields than the control. The overall metal uptake in plant shoots was lower under DC treatment compared to AC treatment and control, although there was a higher accumulation of Zn and Cu in the plant roots treated with electrical fields. The Zn uptake in plant shoots under AC treatment was higher compared to the control and DC treatment. Zn and Cu accumulation in the plant roots under AC and DC treatment was similar, and both were higher comparing to control. Cd content in plant roots under all three treatments was found to be higher than that in the soil. The Pb accumulation in the roots and the uptake into the shoots was lower compared to its content in the soil. PMID:18569305

  12. Highly Efficient Antibacterial and Pb(II) Removal Effects of Ag-CoFe2O4-GO Nanocomposite.

    PubMed

    Ma, Shuanglong; Zhan, Sihui; Jia, Yanan; Zhou, Qixing

    2015-05-20

    Ag-CoFe2O4-graphene oxide (Ag-CoFe2O4-GO) nanocomposite was synthesized by doping silver and CoFe2O4 nanoparticles on the surface of GO, which was used to purify both bacteria and Pb(II) contaminated water. The Ag-CoFe2O4-GO nanomaterial was characterized by transmission electron microscopy (TEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), Raman, X-ray photoelectron spectroscopy (XPS), Brunauer-Emmett-Teller (BET), cyclic voltammetry (CV), and magnetic property tests. It can be found that Ag-CoFe2O4-GO nanocomposite exhibited excellent antibacterial activity against Gram-negative Escherichia coli and Gram-positive Staphylococcus aureus compared with CoFe2O4, Ag-CoFe2O4, and CoFe2O4-GO composite. This superior disinfecting effect was possibly attributed to the combination of GO nanosheets and Ag nanoparticles. Several antibacterial factors including temperature, time, and pH were also investigated. It was obvious that E. coli was more susceptible than S. aureus toward all the four types of nanomaterials. The structural difference of bacterial membranes should be responsible for the resistant discrepancy. We also found that Ag-CoFe2O4-GO inactivated both bacteria in an irreversibly stronger manner than Ag-CoFe2O4 and CoFe2O4-GO. The Pb(II) removal efficiency with all the nanomaterials showed significant dependence on the surface area and zeta potential of the materials. In this work, not only did we demonstrate the simultaneous superior removal efficiency of bacteria and Pb(II) by Ag-CoFe2O4-GO but also the antibacterial mechanism was discussed to have a better understanding of the interaction between Ag-CoFe2O4-GO and bacteria. In a word, taking into consideration the easy magnetic separation, bulk availability, and irreversibly high antibacterial activity of Ag-CoFe2O4-GO, it is the very promising candidate material for advanced antimicrobial or Pb(II) contaminated water treatment.

  13. Measurement of diffusion coefficient using a diaphragm cell: PbBr 2AgBr system

    NASA Astrophysics Data System (ADS)

    Singh, N. B.; Glicksman, M. E.; Coriell, S. R.; Duval, W. M. B.; Santoro, G. J.; DeWitt, R.

    1996-09-01

    The diffusion coefficient of molten lead bromide-silver bromide was determined using a two chamber diaphragm cell separated by the porous membrane of a sintered glass disk. Only dilute mixtures of PbBr 2AgBr were studied. The interdiffusion coefficient was determined to be 1.71 × 10 -5cm 20/s.

  14. Sorption behavior of Cd, Cu, Pb, and Zn and their interactions in phytoremediated soil.

    PubMed

    Trakal, L; Komárek, M; Száková, J; Tlustos, P; Tejnecký, V; Drábek, O

    2012-09-01

    The aim of our study was to compare the sorption properties of a contaminated soil before and after two types of phytoremediation (natural phytoextraction vs. phytostabilization with dolomite limestone (DL) application). Soil from a pot experiment in controlled greenhouse conditions performed for two vegetation periods was used for the study. Lead, as the main contaminant in the studied soil, was easily desorbed by Cu, especially due to the increased affinity of Cu for soil organic matter; hence input of Cu to the studied soil can present another environmental risk in soils contaminated with other metals (such as Pb). In addition, the sorption behavior of chosen metals from single-element solutions differed from multielement solutions. The obtained results proved the different sorption behavior of metals in the single-element solution compared to the multi-element ones. Soil sorption behavior of Cd, Cu, and Zn decreased with the presence of the competitive metals; nevertheless, Pb sorption potential was not influenced by other competitive metals. Natural phytoextraction showed no significant effect on the sorption of Cd, Cu, Pb, and Zn onto the soil On the other hand, phytostabilization associated with DL application improved the soil sorption efficiency of all chosen metals, especially of Cu.

  15. Locating Pb2+ and Zn2+ in Zinc Finger-Like Peptides Using Mass Spectrometry

    NASA Astrophysics Data System (ADS)

    Banu, Laura; Blagojevic, Voislav; Bohme, Diethard K.

    2013-10-01

    The binding preferences of Pb2+and Zn2+ in doubly charged complexes with zinc finger-like 12-residue peptides (Pep), [Mn(Pep-2(n-1)H)]2+ have been explored using tandem mass spectrometry. The peptides were synthesized strategically by blocking the N-terminus with an acetyl group and with four cysteine and/or histidine residues in positions 2, 5, 8, and 11, arranged in different motifs: CCHH, CHCH, and CCCC. The MS2 spectra of the Pb2+ and Zn2+ complexes show multiple losses of water and a single methane loss and these provide a sensitive method for locating the metal dication and so elucidating its coordination. The elimination of a methane molecule indicated the position of the metal at the Cys2 residue. Whereas lead was observed to preferentially bind to cysteine residues, zinc was found to primarily bind to histidine residues and secondarily to cysteine residues. Preferential binding of lead to cysteine is preserved in the complexes with more than one Pb2+. Key to the mechanism of the loss of water and methane is the metal dication withdrawing electrons from the proximal amidic nitrogen. This acidic nitrogen loses its hydrogen to an amidic oxygen situated four atoms away leading to formation of a five-member ring and the elimination of water.

  16. Ag-Modified In₂O₃/ZnO Nanobundles with High Formaldehyde Gas-Sensing Performance.

    PubMed

    Fang, Fang; Bai, Lu; Song, Dongsheng; Yang, Hongping; Sun, Xiaoming; Sun, Hongyu; Zhu, Jing

    2015-01-01

    Ag-modified In2O3/ZnO bundles with micro/nano porous structures have been designed and synthesized with by hydrothermal method continuing with dehydration process. Each bundle consists of nanoparticles, where nanogaps of 10-30 nm are present between the nanoparticles, leading to a porous structure. This porous structure brings high surface area and fast gas diffusion, enhancing the gas sensitivity. Consequently, the HCHO gas-sensing performance of the Ag-modified In2O3/ZnO bundles have been tested, with the formaldehyde-detection limit of 100 ppb (parts per billion) and the response and recover times as short as 6 s and 3 s, respectively, at 300 °C and the detection limit of 100 ppb, response time of 12 s and recover times of 6 s at 100 °C. The HCHO sensing detect limitation matches the health standard limitation on the concentration of formaldehyde for indoor air. Moreover, the strategy to synthesize the nanobundles is just two-step heating and easy to scale up. Therefore, the Ag-modified In2O3/ZnO bundles are ready for industrialization and practical applications. PMID:26287205

  17. Ag-Modified In₂O₃/ZnO Nanobundles with High Formaldehyde Gas-Sensing Performance.

    PubMed

    Fang, Fang; Bai, Lu; Song, Dongsheng; Yang, Hongping; Sun, Xiaoming; Sun, Hongyu; Zhu, Jing

    2015-08-14

    Ag-modified In2O3/ZnO bundles with micro/nano porous structures have been designed and synthesized with by hydrothermal method continuing with dehydration process. Each bundle consists of nanoparticles, where nanogaps of 10-30 nm are present between the nanoparticles, leading to a porous structure. This porous structure brings high surface area and fast gas diffusion, enhancing the gas sensitivity. Consequently, the HCHO gas-sensing performance of the Ag-modified In2O3/ZnO bundles have been tested, with the formaldehyde-detection limit of 100 ppb (parts per billion) and the response and recover times as short as 6 s and 3 s, respectively, at 300 °C and the detection limit of 100 ppb, response time of 12 s and recover times of 6 s at 100 °C. The HCHO sensing detect limitation matches the health standard limitation on the concentration of formaldehyde for indoor air. Moreover, the strategy to synthesize the nanobundles is just two-step heating and easy to scale up. Therefore, the Ag-modified In2O3/ZnO bundles are ready for industrialization and practical applications.

  18. Midinfrared Nonlinear Optical Thiophosphates from LiZnPS4 to AgZnPS4: A Combined Experimental and Theoretical Study.

    PubMed

    Zhou, Molin; Kang, Lei; Yao, Jiyong; Lin, Zheshuai; Wu, Yicheng; Chen, Chuangtian

    2016-04-18

    Our earlier theoretical calculation and preliminary experiment highlighted LiZnPS4 as a good mid-infrared (mid-IR) nonlinear optical (NLO) material. However, this compound suffers from problems including corrosion of the silica tubes, a pungent smell, deliquescence, and incongruent-melting behavior in the further single crystal growth and applications. In order to overcome these problems, herein, we investigate the analogues of LiZnPS4 and propose that AgZnPS4 would be a good candidate. The combination of experimental and theoretical study demonstrates that AgZnPS4 exhibits a much stronger NLO effect than that of LiZnPS4 despite the relatively smaller energy band gap. More importantly, AgZnPS4 melts congruently with a melting point as low as 534 °C, much lower than those of traditional IR NLO crystals, and is nondeliquescent with enough stability in the air. Such a good crystal growth habit and chemical stability enable AgZnPS4 to possess much better overall performance for the practical mid-IR NLO applications. PMID:27015097

  19. Band edge emission enhancement by quadrupole surface plasmon-exciton coupling using direct-contact Ag/ZnO nanospheres.

    PubMed

    Zang, Yashu; He, Xu; Li, Jing; Yin, Jun; Li, Kongyi; Yue, Chuang; Wu, Zhiming; Wu, Suntao; Kang, Junyong

    2013-01-21

    Periodic Ag nanoball (NB) arrays on ZnO hollow nanosphere (HNS) supporting structures were fabricated in a large area by a laser irradiation method. The optimized laser power and spherical supporting structure of ZnO with a certain size and separation were employed to aggregate a sputtering-deposited Ag nano-film into an ordered, large-area, and two dimensional Ag NB array. A significant band edge (BE) emission enhancement of ZnO HNSs was achieved on this Ag NB/ZnO HNS hybrid structure and the mechanism was revealed by further experimental and theoretical analyses. With successfully fabricating the direct-contact structure of a Ag NB on the top of each ZnO HNS, the highly localized quadrupole mode surface plasmon resonance (SPR), realized on the metal NBs in the ultraviolet region, can effectively improve the BE emission of ZnO through strong coupling with the excitons of ZnO. Compared with the dipole mode SPR, the quadrupole mode SPR is insensitive to the metal nanoparticle's size and has a resonance frequency in the BE region of the wide band gap materials, hence, it can be potentially applied in related optoelectronic devices. PMID:23196786

  20. Synthesis of wheatear-like ZnO nanoarrays decorated with Ag nanoparticles and its improved SERS performance through hydrogenation.

    PubMed

    Shan, Yufeng; Yang, Yong; Cao, Yanqin; Fu, Chaoli; Huang, Zhengren

    2016-04-01

    Semiconductor/noble metal composite SERS substrates have been extensively studied due to their unique bifunctionality. In this work, wheatear-like ZnO nanoarrarys have been fabricated via a modified low-temperature solution method. The hierarchical nanostructures that are constructed by stacked nanoflakes and long whiskers of ZnO possess a substantial number of characteristic nano corners and edges, which are proved to be beneficial to deposit more Ag nanoparticles (NPs). Furthermore, hydrogenated wheatear-like ZnO/AgNP composite substrates are achieved via a safe and facile solid hydrogen source (NaBH4). The hydrogenated ZnO/AgNPs (H-ZnO/Ag) substrates exhibit greatly improved SERS activity in detecting R6G molecules with an enhancement factor (EF) up to ∼0.49 × 10(8), over two orders of magnitude higher than that of the substrates before hydrogenation. The outstanding SERS performance of wheatear-like H-ZnO/Ag substrates benefits from the emerging porous structure of ZnO and abundant surface defects introduced by hydrogenation. In addition, the as-prepared substrates also show high detection sensitivity, good repeatability and recyclability, indicating great potential for practical applications. PMID:26916627

  1. Characterization and antibacterial properties of genipin-crosslinked chitosan/poly(ethylene glycol)/ZnO/Ag nanocomposites.

    PubMed

    Liu, Yangshuo; Kim, Hyung-Il

    2012-06-01

    Novel nanocomposites consisting of genipin-crosslinked chitosan (GC), poly(ethylene glycol) (PEG), zinc oxide (ZnO), and silver (Ag) nanoparticles were prepared for biomedical applications as the wound-healing materials. Various amounts of ZnO and Ag nanoparticles were dispersed in the GC/PEG hydrogel matrix without severe aggregation. The effects of composition and ZnO nanoparticles on the physico-chemical properties of nanocomposite samples were evaluated by infrared analysis, X-ray diffraction, and scanning electron microscopy. GC/PEG/ZnO/Ag nanocomposite showed the pH-sensitive swelling behavior and the improved mechanical properties. The antibacterial activities of nanocomposite films were tested toward the bacterial species Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus, and Bacillus subtilis. GC/PEG/ZnO/Ag composite films had higher antibacterial activities than GC/PEG and GC/PEG/ZnO nanocomposite films. GC/PEG/ZnO/Ag composite films have potential application as wound and burn dressings. PMID:24750611

  2. Tunable Visible Emission of Ag-Doped CdZnS Alloy Quantum Dots

    PubMed Central

    2010-01-01

    Highly luminescent Ag-ion-doped Cd1−xZnxS (0 ≤ x ≤ 1) alloy nanocrystals were successfully synthesized by a novel wet chemical precipitation method. Influence of dopant concentration and the Zn/Cd stoichiometric variations in doped alloy nanocrystals have been investigated. The samples were characterized by X-ray diffraction (XRD) and high resolution transmission electron microscope (HRTEM) to investigate the size and structure of the as prepared nanocrystals. A shift in LO phonon modes from micro-Raman investigations and the elemental analysis from the energy dispersive X-ray analysis (EDAX) confirms the stoichiometry of the final product. The average crystallite size was found increasing from 1.0 to 1.4 nm with gradual increase in Ag doping. It was observed that photoluminescence (PL) intensity corresponding to Ag impurity (570 nm), relative to the other two bands 480 and 520 nm that originates due to native defects, enhanced and showed slight red shift with increasing silver doping. In addition, decrease in the band gap energy of the doped nanocrystals indicates that the introduction of dopant ion in the host material influence the particle size of the nanocrystals. The composition dependent bandgap engineering in CdZnS:Ag was achieved to attain the deliberate color tunability and demonstrated successfully, which are potentially important for white light generation. PMID:20652135

  3. Electrostatic Assembly of Sandwich-like Ag-C@ZnO-C@Ag-C Hybrid Hollow Microspheres with Excellent High-Rate Lithium Storage Properties.

    PubMed

    Xie, Qingshui; Ma, Yating; Wang, Xuanpeng; Zeng, Deqian; Wang, Laisen; Mai, Liqiang; Peng, Dong-Liang

    2016-01-26

    Herein, we introduce a facile electrostatic attraction approach to produce zinc-silver citrate hollow microspheres, followed by thermal heating treatment in argon to ingeniously synthesize sandwich-like Ag-C@ZnO-C@Ag-C hybrid hollow microspheres. The 3D carbon conductive framework in the hybrids derives from the in situ carbonation of carboxylate acid groups in zinc-silver citrate hollow microspheres during heating treatment, and the continuous and homogeneous Ag nanoparticles on the outer and inner surfaces of hybrid hollow microspheres endow the shells with the sandwiched configuration (Ag-C@ZnO-C@Ag-C). When applied as the anode materials for lithium ion batteries, the fabricated hybrid hollow microspheres with sandwich-like shells reveal a very large reversible capacity of 1670 mAh g(-1) after 200 cycles at a current density of 0.2 A g(-1). Even at the very large current densities of 1.6 and 10.0 A g(-1), the high specific capacities of about 1063 and 526 mAh g(-1) can be retained, respectively. The greatly enhanced electrochemical properties of Ag-C@ZnO-C@Ag-C hybrid microspheres are attributed to their special structural features such as the hollow structures, the sandwich-like shells, and the nanometer-sized building blocks.

  4. A study of the microstructure, thermal properties and wetting kinetics of Sn-3Ag- xZn lead-free solders

    NASA Astrophysics Data System (ADS)

    Li, Yulong; Yu, Xiao; Sekulic, Dusan P.; Hu, Xiaowu; Yan, Ming; Hu, Ronghua

    2016-06-01

    Microstructure, thermal properties and wetting kinetics of Sn-3Ag- xZn solders ( x = 0.4, 0.6, 0.8, 1, 2 and 4 wt%) were systematically investigated. The results indicate that a small amount of Zn (Zn wt% ≤ 1 wt%) has a rather moderate effect on the microstructure morphology of the Sn-3Ag- xZn solders. The microstructures are composed of a β-Sn phase and the mixture of Ag3Sn and ζ-AgZn particles. However, the β-Sn phase reduces its volume fraction in the entire microstructure and the intermetallic compounds population increases with the increasing of Zn content. The microstructure is dramatically changed with a further increase in the Zn content. The γ-AgZn phase is formed in a Sn-3Ag-2Zn solder. The ɛ-AgZn phase is formed in a Sn-3Ag-4Zn solder. The melting temperature and the undercooling of the Sn-3Ag- xZn solder alloys decrease with the increase in Zn content, reach to a minimum value when the content of Zn is 1 wt%, and then increase with further increase in Zn content. The Sn-3Ag-1Zn demonstrates the minimum value of 228.13 °C in the melting temperature and 13.87 °C in undercooling. The wetting kinetics of the main spreading stage features the power law of R n ~ t ( n = 1), which is controlled by chemical reactions at the triple line.

  5. Multiple site study of recent atmospheric metal (Pb, Zn and Cu) deposition in the NW Iberian Peninsula using peat cores.

    PubMed

    Olid, Carolina; Garcia-Orellana, Jordi; Martínez-Cortizas, Antonio; Masqué, Pere; Peiteado-Varela, Eva; Sanchez-Cabeza, Joan-Albert

    2010-10-15

    In order to estimate atmospheric metal deposition in Southern Europe since the beginning of the Industrial Period (~1850 AD), concentration profiles of Pb, Zn and Cu were determined in four (210)Pb-dated peat cores from ombrotrophic bogs in Serra do Xistral (Galicia, NW Iberian Peninsula). Maximum metal concentrations varied by a factor of 1.8 for Pb and Zn (70 to 128μgg(-1) and 128 to 231μgg(-1), respectively) and 3.5 for Cu (11 to 37μgg(-1)). The cumulative metal inventories of each core varied by a factor of 3 for all analysed metals (132 to 329μgcm(-2) for Pb, 198 to 625μgcm(-2) for Zn and 22 to 69μgcm(-2) for Cu), suggesting differences in net accumulation rates among peatlands. Although results suggest that mean deposition rates vary within the studied area, the enhanced (210)Pb accumulation and the interpretation of the inventory ratios ((210)Pb/Pb, Zn/Pb and Cu/Pb) in two bogs indicated that either a record perturbation or post-depositional redistribution effects must be considered. After correction, Pb, Zn and Cu profiles showed increasing concentrations and atmospheric fluxes since the mid-XX(th) century to maximum values in the second half of the XX(th) century. For Pb, maximum fluxes were observed in 1955-1962 and ranged from 16 to 22mgm(-2)yr(-1) (mean of 18±1mgm(-2)yr(-1)), two orders of magnitude higher than in the pre-industrial period. Peaks in Pb fluxes in Serra do Xistral before the period of maximum consumption of leaded petrol in Europe (1970s-1980s) suggest the dominance of local pollutant sources in the area (i.e. coal mining and burning). More recent peaks were observed for Zn and Cu, with fluxes ranging from 32 to 52mgm(-2)yr(-1) in 1989-1996, and from 4 to 9mgm(-2)yr(-1) in 1994-2001, respectively. Our results underline the importance of multi-core studies to assess both the integrity and reliability of peat records, and the degree of homogeneity in bog accumulation. We show the usefulness of using the excess (210)Pb inventory to

  6. Geological, rare earth elemental and isotopic constraints on the origin of the Banbanqiao Zn-Pb deposit, southwest China

    NASA Astrophysics Data System (ADS)

    Li, Bo; Zhou, Jia-Xi; Huang, Zhi-Long; Yan, Zai-Fei; Bao, Guang-Ping; Sun, Hai-Rui

    2015-11-01

    The newly discovered Banbanqiao Zn-Pb deposit in the southeastern part of the Sichuan-Yunnan-Guizhou (SYG) Pb-Zn metallogenic province is located on the western Yangtze Block, southwest China. Ore bodies of the Banbanqiao deposit are stratiform type, host in dolomitic limestone and dolostone of the Lower Carboniferous Dapu Formation and occur within the NNE-trending Banbanqiao anticline. More than 1.5 million tones (Mt) Zn-Pb ores at grades of 0.26-10.32 wt.% Pb and 0.81-28.8 wt.% Zn have been controlled until now. δ13CPDB and δ18OSMOW values of calcite separates range from -2.8‰ to -0.7‰ (average -1.1‰) and +14.1‰ to +17.0‰ (average +15.5‰), respectively. The δ13CPDB values are similar to those of marine carbonate rocks, but higher than those of mantle and significantly different from those of sedimentary organic matter. However, the δ18OSMOW values are among those of mantle, marine carbonate rocks and sedimentary organic matter. δ34SCDT values of sulfide separates range from +3.2‰ to +9.9‰ (average +6.5‰), unlike mantle-derived sulfur (0 ± 3‰), whilst lower than evaporites (+22‰ to +28‰) within host strata. 206Pb/204Pb, 207Pb/204Pb and 208Pb/204Pb values of country shale and dolostone whole-rock samples are 18.47, 15.66 and 38.70, and 18.44-18.60, 15.66-15.85 and 38.70-39.14, respectively. Sulfide separates have 206Pb/204Pb, 207Pb/204Pb and 208Pb/204Pb values ranging from 18.03 to 18.73, 15.65 to 15.78 and 38.15 to 39.14, respectively. These Pb isotopic data indicate a clearly crustal source of Pb in the plot of 207Pb/204Pb vs. 206Pb/204Pb. Total REE (ΣREE) contents of country shale and dolostone whole-rock samples are 2.63 ppm and 0.72-86.2 ppm with δEu values are 2.79 and 0.34-0.70, respectively. Pyrite, sphalerite, galena and calcite samples have ΣREE contents of 5.3-36.4 ppm, 0.29-3.39 ppm, 0.52 ppm and 22.0-41.1 ppm, respectively, and δEu values of 0.64-0.86, 0.94-2.86, 0.32 and 0.21-0.45, respectively. These rare earth

  7. Martensitic transformation behavior in Ti–Ni–X (Ag, In, Sn, Sb, Te, Tl, Pb, Bi) ternary alloys

    SciTech Connect

    Jang, Jai-young; Chun, Su-jin; Kim, Nam-suk; Cho, Jeung-won; Kim, Jae-hyun; Yeom, Jong-taek; Kim, Jae-il; Nam, Tae-hyun

    2013-12-15

    Graphical abstract: - Highlights: • Ag, In and Sn were soluble in TiNi matrix, while Sb, Te, Tl, Pb and Bi were not. • The B2-R-B19′transformation occurred in Ti-Ni-(Ag, In, Sn) alloys. • Solid solution hardening was essential for inducing the B2-R transformation. - Abstract: The microstructures and transformation behaviors of Ti–Ni–X (Ag, In, Sn, Sb, Te, Tl, Pb, Bi) ternary alloys were investigated using electron probe micro-analysis (EPMA), X-ray diffraction (XRD), differential scanning calorimetry (DSC) and Micro Vickers hardness tests. All specimens consisted of Ti–Ni matrices and second phase particles. Ag, In and Sn were soluble in Ti–Ni matrices with a limited solubility (≤1.0 at%), while Sb, Te, Tl, Pb and Bi were not soluble. Two-stage B2-R-B19′ transformation occurred in Ti–48.8Ni–1.2Ag, Ti–49.0Ni–1.0In and Ti–49.0Ni–1.0Sn alloys, while one-stage B2-B19′ transformation occurred in Ti–49.0Ni–1.0Ag, Ti–49.0Ni–1.0Sb, Ti–49.0Ni–1.0Te, Ti–49.0Ni–1.0Pb and Ti–49.0Ni–1.0Bi alloys. Micro Vickers hardness of the alloys displaying the B2-R-B19′ transformation (Hv 250–368) was much larger than that (

  8. Ultrathin single-crystal ZnO nanobelts: Ag-catalyzed growth and field emission property

    NASA Astrophysics Data System (ADS)

    Xing, G. Z.; Fang, X. S.; Zhang, Z.; Wang, D. D.; Huang, X.; Guo, J.; Liao, L.; Zheng, Z.; Xu, H. R.; Yu, T.; Shen, Z. X.; Huan, C. H. A.; Sum, T. C.; Zhang, H.; Wu, T.

    2010-06-01

    We report the growth of ultrathin single-crystal ZnO nanobelts by using a Ag-catalyzed vapor transport method. Extensive transmission electron microscopy and atomic force microscopy measurements reveal that the thickness of the ultrathin ZnO nanobelts is ~ 2 nm. Scanning electron microscopy and post-growth annealing studies suggest a '1D branching and 2D filling' growth process. Our results demonstrate the critical role of catalyst in the deterministic synthesis of nanomaterials with the desired morphology. In addition, these ultrafine nanobelts exhibit stable field emission with unprecedented high emission current density of 40.17 mA cm - 2. These bottom-up building blocks of ultrathin ZnO nanobelts may facilitate the construction of advanced electronic and photonic nanodevices.

  9. Concentrations of Pb, Zn, and Cu in Taraxacum spp. in relation to urban pollution

    SciTech Connect

    Cook, C.M.; Lanaras, T.; Sgardelis, S.P.; Pantis, J.D. )

    1994-08-01

    The combustion of petroleum fuel and exhaust emissions are major sources of atmospheric pollution in cities which result in the deposition of toxic substances, particularly heavy metals, in the surface layers of soils. Lead in particular enters the environment from the use of tetraethyl lead as an antiknock agent for petrol engines constituting 21% of fine particles emitted from cars burning leaded petrol. Antiwear protectants incorporated in lubricants often contain Cd, Cr, Cu, Hg, Ni, Pb and/or Zn which are also released into the environment by inefficient engines and irresponsible dumping of engine oils. Zn from tyre wear and Cu from diesel engines also add considerably to the environmental metal burden. Lowering of the permitted lead content of petrol and the growing use of unleaded fuel are expected to lead to reductions in the environmental lead burden, however, until unleaded fuel becomes universally accepted lead contamination, particularly of roadside soils and vegetation is a major cause for concern. A direct relationship between car exhaust, the Pb content of needles of Abies alba and reduced growth has been observed and can extend hundreds of metres from major highways. Lead tolerance has been observed in higher plants growing mine waste soils and to a lesser extent on lead-contaminated roadside soils. Automobiles which are responsible for line sources of pollution emissions in rural and suburban areas have a more far-reaching impact on roadside vegetation, already under considerable stress, in urban areas. Information on heavy metal effects on vegetation in urban environments however, are scarce. Modeling and multivariate analysis of a few of the factors involved have provided only limited data related to plant performance in these complex environments. Therefore in this study, the extent of heavy metal pollution by Pb, Zn, Cu and Cd in soils and in dandelion plants in the city of Thessaloniki has been examined. 20 refs., 2 figs., 3 tabs.

  10. Ultrasonic semi-solid coating soldering 6061 aluminum alloys with Sn-Pb-Zn alloys.

    PubMed

    Yu, Xin-ye; Xing, Wen-qing; Ding, Min

    2016-07-01

    In this paper, 6061 aluminum alloys were soldered without a flux by the ultrasonic semi-solid coating soldering at a low temperature. According to the analyses, it could be obtained that the following results. The effect of ultrasound on the coating which promoted processes of metallurgical reaction between the components of the solder and 6061 aluminum alloys due to the thermal effect. Al2Zn3 was obtained near the interface. When the solder was in semi-solid state, the connection was completed. Ultimately, the interlayer mainly composed of three kinds of microstructure zones: α-Pb solid solution phases, β-Sn phases and Sn-Pb eutectic phases. The strength of the joints was improved significantly with the minimum shear strength approaching 101MPa.

  11. Ultrasonic semi-solid coating soldering 6061 aluminum alloys with Sn-Pb-Zn alloys.

    PubMed

    Yu, Xin-ye; Xing, Wen-qing; Ding, Min

    2016-07-01

    In this paper, 6061 aluminum alloys were soldered without a flux by the ultrasonic semi-solid coating soldering at a low temperature. According to the analyses, it could be obtained that the following results. The effect of ultrasound on the coating which promoted processes of metallurgical reaction between the components of the solder and 6061 aluminum alloys due to the thermal effect. Al2Zn3 was obtained near the interface. When the solder was in semi-solid state, the connection was completed. Ultimately, the interlayer mainly composed of three kinds of microstructure zones: α-Pb solid solution phases, β-Sn phases and Sn-Pb eutectic phases. The strength of the joints was improved significantly with the minimum shear strength approaching 101MPa. PMID:26964943

  12. Si/ZnO nanorods/Ag/AZO structures as promising photovoltaic plasmonic cells

    SciTech Connect

    Placzek-Popko, E. Gwozdz, K.; Gumienny, Z.; Zielony, E.; Jacak, W.; Pietruszka, R.; Witkowski, B. S.; Wachnicki, Ł.; Gieraltowska, S.; Chang, Liann-Be

    2015-05-21

    The test structures for photovoltaic (PV) applications based on zinc oxide nanorods (NRs) that were grown using a low-temperature hydrothermal method on p-type silicon substrates (100) covered with Ag nanoparticles (NPs) were studied. The NPs of three different diameters, i.e., 5–10 nm, 20-30 nm, and 50–60 nm, were deposited using a sputtering method. The morphology and crystallinity of the structures were confirmed by scanning electron microscopy and Raman spectroscopy. It was found that the nanorods have a hexagonal wurtzite structure. An analysis of the Raman and photoluminescence spectra permitted the identification of the surface modes at 476 cm{sup −1} and 561 cm{sup −1}. The presence of these modes is evidence of nanorods oriented along the wurtzite c-axis. The NRs with Ag NPs were covered with a ZnO:Al (AZO) layer that was grown using the low-temperature atomic layer deposition technique. The AZO layer served as a transparent ohmic contact to the ZnO nanorods. The applicability of the AZO layer for this purpose and the influence of the Ag nanoparticles on the effectiveness of light acquisition by such prepared PV cells were checked by reflectance and transmittance measurements of the AZO/glass and AZO/NPs/glass reference structures. Based on these studies, the high-energy transmittance edge was assigned to the ZnO energy gap, although it is blueshifted with respect to the bulk ZnO energy gap because of Al doping. It was also shown that the most optimal PV performance is obtained from a structure containing Ag nanoparticles with a diameter of 20–30 nm. This result is confirmed by the current-voltage measurements performed with 1-sun illumination. The structures show a plasmonic effect within the short wavelength range: the PV response for the structure with Ag nanoparticles is twice that of the structure without the nanoparticles. However, the influence of the Ag nanoparticle diameters on the plasmonic effect is ambiguous.

  13. Distribution and evolution of Zn, Cd, and Pb in Apollo 16 regolith samples and the average U-Pb ages of the parent rocks

    NASA Technical Reports Server (NTRS)

    Cirlin, E. H.; Housley, R. M.

    1982-01-01

    The concentration of surface (low temperature site) and interior (high temperature site) Cd, Zn, and Pb in 13 Apollo 16 highland fines samples, pristine rock 65325, and mare fines sample 75081 were analyzed directly from the thermal release profiles obtained by flameless atomic absorption technique (FLAA). Cd and Zn in pristine ferroan anothosite 65325, anorthositic grains of the most mature fines 65701, and basaltic rock fragments of mare fines 75081 were almost all surface Cd and Zn indicating that most volatiles were deposited on the surfaces of vugs, vesicles and microcracks during the initial cooling process. A considerable amount of interior Cd and Zn was observed in agglutinates. This result suggests that high temperature site interior volatiles originate from entrapment during the lunar maturation processes. Interior Cd found in the most mature fines sample 65701 was only about 15% of the total Cd in the sample. Interior Pb present in Apollo 16 fines samples went up to 60%. From our Cd studies we can assume that this interior Pb in highland fines samples is largely due to the radiogenic decay which occurred after the redistribution of the volatiles took place. We obtained an average age of 4.0 b.y. for the parent rocks of Apollo 16 highland regolith from our interior Pb analyses.

  14. Removal of Pb(II) and Zn(II) from Aqueous Solutions by Raw Crab Shell: A Comparative Study.

    PubMed

    Zhou, Chuanqiang; Gong, Xiangxiang; Han, Jie; Guo, Rong

    2016-04-01

    Removals of Pb(II) and Zn(II) ions from water using crab (Clistocoeloma sinensis) shell particles as biosorbent have been compared in this study. Uptake equilibriums for two ions well described by Langmuir isotherm revealed that crab shell possessed higher uptake capacity for Pb(II) (709 mg/g) than that for Zn(II) (117 mg/g). Kinetics data for the uptake of the two metals were successfully modeled using the pseudo-second-order model, where the initial uptake rate of Pb(II) was much faster than that of Zn(II). Dubinin-Radushkevick modeling and thermodynamic parameters hinted at different uptake mechanisms of Pb(II) and Zn(II) removal by crab shell, attested by FTIR, XRD, FESEM analysis. Pb(II) ion was removed mainly through the chemical reaction, while the uptake of Zn(II) ion onto crab shell was attributed to the chelation and coordination interactions. The polluted river water and laboratory wastewater both satisfied the standards for drinking and irrigation/fishery water, respectively, after being treated with crab shell particles.

  15. Heavy metal distribution and chemical speciation in tailings and soils around a Pb-Zn mine in Spain.

    PubMed

    Rodríguez, L; Ruiz, E; Alonso-Azcárate, J; Rincón, J

    2009-02-01

    Soil pollution by lead, zinc, cadmium and copper was characterized in the mine tailings and surrounding soils (arable and pasture lands) of an old Spanish Pb-Zn mine. Sixty soil samples were analyzed, determining the total metal concentration by acid digestion and the chemical fractionation of Pb and Zn by the modified BCR sequential extraction method. Samples belonging to mine waste areas showed the highest values, with mean concentrations of 28,453.50 mg kg(-1) for Pb, 7000.44 mg kg(-1) for Zn, 20.57 mg kg(-1) for Cd and 308.48 mg kg(-1) for Cu. High concentrations of Pb, Zn and Cd were found in many of the samples taken from surrounding arable and pasture lands, indicating a certain extent of spreading of heavy metal pollution. Acidic drainage and wind transport of dust were proposed as the main effects causing the dispersion of pollution. Sequential extraction showed that most of the Pb was associated with non-residual fractions, mainly in reducible form, in all the collected samples. Zn appeared mainly associated with the acid-extractable form in mine tailing samples, while the residual form was the predominant one in samples belonging to surrounding areas. Comparison of our results with several criteria reported in the literature for risk assessment in soils polluted by heavy metals showed the need to treat the mine tailings dumped in the mine area.

  16. Pb2+ and Zn2+ adsorption by a natural aluminum- and iron-bearing surface coating on an aquifer sand

    USGS Publications Warehouse

    Coston, J.A.; Fuller, C.C.; Davis, J.A.

    1995-01-01

    Pb2+ and Zn2+ adsorption was studied in batch experiments with material collected from a shallow, unconfined aquifer of glacial outwash sand and gravel in Falmouth, Massachusetts, USA. The aquifer solids contain primarily quartz with minor amounts of alkali feldspars and ferromagnetic minerals. Pb2+ and Zn2+ adsorption experiments with various grain size and mineral fractions of the aquifer solids showed that: 1) Zn2+ adsorption was independent of grain size, but Pb2+ was preferentially adsorbed by the <64 ??m size fraction and 2) Pb2+ adsorption decreased after removal of the paramagnetic, Fe-bearing mineral fraction, but Zn2+ adsorption was unaffected. Pb2+ and Zn2+ adsorption on mineral separates from the aquifer material compared with metal adsorption on a purified quartz powder indicated that adsorption of both metal ions was dominated by coatings on the quartz fraction of the sediment. Characterization of the coatings by AES, SEM-EDS, and TOF-SIMS demonstrated that the natural quartz grains were extensively coated with Al- and Fe-bearing minerals of variable composition. -from Authors

  17. U-Pb geochronology, geochemistry, and H-O-S-Pb isotopic compositions of the Leqingla and Xin'gaguo skarn Pb-Zn polymetallic deposits, Tibet, China

    NASA Astrophysics Data System (ADS)

    Wang, Liqiang; Cheng, Wenbin; Tang, Juxing; Kang, Haoran; Zhang, Yan; Li, Zhuang

    2016-01-01

    The Leqingla and Xin'gaguo deposits are two representative skarn Pb-Zn polymetallic deposits of the Gangdese Pb-Zn polymetallic belt, Tibet, China. LA-ICP-MS zircon U-Pb dating of the mineralization-related biotite granites from both the Leqingla and Xin'gaguo deposits yielded weighted mean ages of 60.8 Ma and 56.5 Ma, respectively, which can be inferred as their mineralization ages. The Leqingla biotite granite is characterized by high Al2O3, total Fe, Na2O, and low K2O. In comparison, the Xin'gaguo biotite granite is characterized by relative higher K2O but lower Al2O3, total Fe, and Na2O. Geochemical and mineralogical characteristics indicate that the Leqingla and Xin'gaguo biotite granites are calc-alkaline I-type granite and High K calc-alkaline I-type granite, respectively. Both the Leqingla and Xin'gaguo biotite granites are enrichment in LREE and LILEs and depletion in HFSEs, and they were formed at the India-Asia collision stage. δ18O and δD values for the Leqingla and Xin'gaguo deposits are -8.8‰ to 5.3‰ and -140.4‰ to -90.1‰, -4.5‰ to 7.0‰ and -117.3‰ to -81.0‰, respectively, indicating magma fluids mixed with meteoric water in ore-forming fluids. δ34S values (-11.6‰ to -0.3‰) of ore sulfides from the Leqingla deposit show characteristics of biogenetic sulfur isotope compositions, suggesting sulfur for the Leqingla deposit were sourced from wall rocks of the Mengla and Luobadui Formation, which are rich in organic materials. δ34S values of ore sulfides from the Xin'gaguo deposits show bimodal distribution (-5.0‰ to -1.6‰ and 1.6-2.1‰), indicating sulfur in the Xin'gaguo deposit were derived from both wall rocks and magma. In the Leqingla deposit, most ore sulfides have the similar Pb isotopic compositions with that of the mineralization-related biotite granite, suggesting the biotite granite supplied most of the ore-forming metals. Pb isotopic compositions of ore sulfides and Hf isotopic compositions of biotite granite show

  18. Determining provenance of marine metal pollution in French bivalves using Cd, Zn and Pb isotopes

    NASA Astrophysics Data System (ADS)

    Shiel, Alyssa E.; Weis, Dominique; Cossa, Daniel; Orians, Kristin J.

    2013-11-01

    Cadmium, Zn and Pb isotopic compositions (MC-ICP-MS) and elemental concentrations (HR-ICP-MS) have been used to distinguish between natural and anthropogenic sources of these metals in bivalves collected from the coastlines of France (English Channel, Atlantic and Mediterranean coasts). The Cd isotopic signatures (δ114Cd = -1.08‰ to -0.52‰) exhibited by bivalves from the coastlines of France, excluding those from NE France, are within the range of those exhibited by bivalves from the USA East coast (δ114Cd = -1.20‰ to -0.54‰). This indicates the high prevalence of industry, as well as the low natural contributions of Cd from North Atlantic waters in both regions. Thus, the significance of anthropogenic Cd sources is similar. These significant anthropogenic contributions are identified for bivalves with a large range in tissue Cd concentrations. Importantly, French bivalves from the Gironde estuary and Marennes-Oléron basin (regions of historic and modern importance for oyster farming, respectively) exhibited the highest Cd levels of the study. Their Cd isotopic signatures indicate historical smelting emissions remain the primary Cd source despite the cessation of local smelting activities in 1986 and subsequent remedial efforts. No significant variability is observed in the δ66Zn values of the French bivalves (∼0.53‰), with the exception of the much heavier compositions exhibited by oysters from the polluted Gironde estuary (1.19-1.27‰). Lead isotopes do not fractionate during processing like Cd and Zn. They can, therefore, be used to identify emissions from industrial processes and the consumption of unleaded gasoline and diesel fuel as metal sources to French bivalves. Cadmium and Zn isotopes are successfully used here as tracers of anthropogenic processing emissions and are combined with Pb isotope "fingerprinting" techniques to identify metal sources.

  19. Self-assembled Ag nanoparticle network passivated by a nano-sized ZnO layer for transparent and flexible film heaters

    SciTech Connect

    Seo, Ki-Won; Kim, Han-Ki; Kim, Min-Yi; Chang, Hyo-Sik

    2015-12-15

    We investigated a self-assembled Ag nanoparticle network electrode passivated by a nano-sized ZnO layer for use in high-performance transparent and flexible film heaters (TFFHs). The low temperature atomic layer deposition of a nano-sized ZnO layer effectively filled the uncovered area of Ag network and improved the current spreading in the self-assembled Ag network without a change in the sheet resistance and optical transmittance as well as mechanical flexibility. The time-temperature profiles and heat distribution analysis demonstrate that the performance of the TFTH with the ZnO/Ag network is superior to that of a TFFH with Ag nanowire electrodes. In addition, the TFTHs with ZnO/Ag network exhibited better stability than the TFFH with a bare Ag network due to the effective current spreading through the nano-sized ZnO layer.

  20. Native plant communities in an abandoned Pb-Zn mining area of northern Spain: implications for phytoremediation and germplasm preservation.

    PubMed

    Barrutia, O; Artetxe, U; Hernández, A; Olano, J M; García-Plazaola, J I; Garbisu, C; Becerril, J M

    2011-03-01

    Plants growing on metalliferous soils from abandoned mines are unique because of their ability to cope with high metal levels in soil. In this study, we characterized plants and soils from an abandoned Pb-Zn mine in the Basque Country (northern Spain). Soil in this area proved to be deficient in major macronutrients and to contain toxic levels of Cd, Pb, and Zn. Spontaneously growing native plants (belonging to 31 species, 28 genera, and 15 families) were botanically identified. Plant shoots and rhizosphere soil were sampled at several sites in the mine, and analyzed for Pb, Zn and Cd concentration. Zinc showed the highest concentrations in shoots, followed by Pb and Cd. Highest Zn concentrations in shoots were found in the Zn-Cd hyperaccumulator Thlaspi caerulescens (mean = 18,254 mg Zn kg(-1) DW). Different metal tolerance and accumulation patterns were observed among the studied plant species, thus offering a wide germplasm assortment for the suitable selection of phytoremediation technologies. This study highlights the importance of preserving metalliferous environments as they shelter a unique and highly valuable metallicolous biodiversity.

  1. Ag nanoparticle-ZnO nanowire hybrid nanostructures as enhanced and robust antimicrobial textiles via a green chemical approach.

    PubMed

    Li, Zhou; Tang, Haoying; Yuan, Weiwei; Song, Wei; Niu, Yongshan; Yan, Ling; Yu, Min; Dai, Ming; Feng, Siyu; Wang, Menghang; Liu, Tengjiao; Jiang, Peng; Fan, Yubo; Wang, Zhong Lin

    2014-04-11

    A new approach for fabrication of a long-term and recoverable antimicrobial nanostructure/textile hybrid without increasing the antimicrobial resistance is demonstrated. Using in situ synthesized Ag nanoparticles (NPs) anchored on ZnO nanowires (NWs) grown on textiles by a 'dip-in and light-irradiation' green chemical method, we obtained ZnONW@AgNP nanocomposites with small-size and uniform Ag NPs, which have shown superior performance for antibacterial applications. These new Ag/ZnO/textile antimicrobial composites can be used for wound dressings and medical textiles for topical and prophylactic antibacterial treatments, point-of-use water treatment to improve the cleanliness of water and antimicrobial air filters to prevent bioaerosols accumulating in ventilation, heating, and air-conditioning systems.

  2. Ag nanoparticle-ZnO nanowire hybrid nanostructures as enhanced and robust antimicrobial textiles via a green chemical approach

    NASA Astrophysics Data System (ADS)

    Li, Zhou; Tang, Haoying; Yuan, Weiwei; Song, Wei; Niu, Yongshan; Yan, Ling; Yu, Min; Dai, Ming; Feng, Siyu; Wang, Menghang; Liu, Tengjiao; Jiang, Peng; Fan, Yubo; Wang, Zhong Lin

    2014-04-01

    A new approach for fabrication of a long-term and recoverable antimicrobial nanostructure/textile hybrid without increasing the antimicrobial resistance is demonstrated. Using in situ synthesized Ag nanoparticles (NPs) anchored on ZnO nanowires (NWs) grown on textiles by a ‘dip-in and light-irradiation’ green chemical method, we obtained ZnONW@AgNP nanocomposites with small-size and uniform Ag NPs, which have shown superior performance for antibacterial applications. These new Ag/ZnO/textile antimicrobial composites can be used for wound dressings and medical textiles for topical and prophylactic antibacterial treatments, point-of-use water treatment to improve the cleanliness of water and antimicrobial air filters to prevent bioaerosols accumulating in ventilation, heating, and air-conditioning systems.

  3. Efficient enhancement of hydrogen production by Ag/Cu2O/ZnO tandem triple-junction photoelectrochemical cell

    NASA Astrophysics Data System (ADS)

    Liu, Ying; Ren, Feng; Shen, Shaohua; Fu, Yanming; Chen, Chao; Liu, Chang; Xing, Zhuo; Liu, Dan; Xiao, Xiangheng; Wu, Wei; Zheng, Xudong; Liu, Yichao; Jiang, Changzhong

    2015-03-01

    Highly efficient semiconductor photoelectrodes for solar hydrogen production through photocatalytic water splitting are a promising and challenge solution to solve the energy problems. In this work, Ag/Cu2O/ZnO tandem triple-junction photoelectrode was designed and prepared. An increase of 11 times of photocurrent is achieved in the Ag/Cu2O/ZnO photoelectrode comparing to that of the Cu2O film. The high performance of the Ag/Cu2O/ZnO film is due to the optimized design of the tandem triple-junction structure, where the localized surface Plasmon resonance of Ag and the hetero-junctions efficiently absorb solar energy, produce, and separate electron-hole pairs in the photocathode.

  4. Effect of mesh patterning with UV pulsed-laser on optical and electrical properties of ZnO/Ag-Ti thin films

    NASA Astrophysics Data System (ADS)

    Kao, K. S.; Cheng, D. L.; Chang, S. H.; Hsieh, P. T.; Chin, H. S.; Lin, H. K.

    2010-10-01

    In this study, the ZnO/Ag-Ti structure for transparence conducting oxide (TCO) is investigated by optimizing the thickness of the Ag-Ti alloy and ZnO layers. The Ag-Ti thin film is deposited by DC magnetron sputtering and its thicknesses is well controlled. The ZnO thin film is prepared by sol-gel method using zinc acetate as cation source, 2-methoxiethanol as solvent and monoethanolamine as solution stabilizer. The ZnO film deposition is performed by spin-coating technique and dried at 150 °C on Corning 1737 glass. Due to the conductivity of ZnO/Ag-Ti is dominated by Ag-Ti, the sheet resistance of ZnO/Ag-Ti decrease dramatically as the thickness of Ag-Ti layer increases. However, the transmittances of ZnO/Ag-Ti become unacceptable for TCO application after the thickness of Ag-Ti layer beyond 6 nm. The as-deposited ZnO/Ag-Ti structure has the optical transmittance of 83% @ 500 nm and the low resistivity of 1.2 × 10 -5 Ω-cm. Furthermore, for improving the optical and electrical properties of ZnO/Ag-Ti, the thermal treatment using laser is adopted. Experimental results indicate that the transmittance of ZnO/Ag-Ti is improved from 83% to 89% @ 500 nm with resistivity of 1.02 × 10 -5 Ω-cm after laser drilling. The optical spectrum, the resistance, and the morphology of the ZnO/Ag-Ti will be reported in the study.

  5. Spectroscopic studies on photoelectron transfer from 2-(furan-2-yl)-1-phenyl-1H-phenanthro[9,10-d]imidazole to ZnO, Cu-doped ZnO and Ag-doped ZnO.

    PubMed

    Thanikachalam, V; Arunpandiyan, A; Jayabharathi, J; Karunakaran, C; Ramanathan, P

    2014-09-01

    The 2-(furan-2-yl)-1-phenyl-1H-phenanthro[9,10-d]imidazole [FPI] has been designed and synthesized as fluorescent sensor for nanoparticulate ZnO. The present work investigates the photoelectron transfer (PET) from FPI to ZnO, Cu-doped ZnO and Ag- doped ZnO nanoparticles using electronic and life time spectral measurements. Broad absorption along with red shift indicates the formation of charge-transfer complex [FPI-Nanoparticles]. The photophysical studies indicate lowering of HOMO and LUMO energy levels of FPI on adsorption on ZnO due to FPI- ZnO interaction. The obtained binding constant implies that the binding of FPI with nanoparticles was influenced by the surface modification of ZnO nanoparticles with Cu and Ag.

  6. Low temperature preparation of Ag-doped ZnO nanowire arrays for sensor and light-emitting diode applications

    NASA Astrophysics Data System (ADS)

    Lupan, O.; Viana, B.; Cretu, V.; Postica, V.; Adelung, R.; Pauporté, T.

    2016-02-01

    Transition metal doped-oxide semiconductor nanostructures are important to achieve enhanced and new properties for advanced applications. We describe the low temperature preparation of ZnO:Ag nanowire/nanorod (NW/NR) arrays by electrodeposition at 90 °C. The NWs have been characterized by SEM, EDX, transmittance and photoluminescence (PL) measurements. The integration of Ag in the crystal is shown. Single nanowire/nanorod of ZnO:Ag was integrated in a nanosensor structure leading to new and enhanced properties. The ultraviolet (UV) response of the nanosensor was investigated at room temperature. Experimental results indicate that ZnO:Ag (0.75 μM) nanosensor possesses faster response/recovery time and better response to UV light than those reported in literature. The sensor structure has been also shown to give a fast response for the hydrogen detection with improved performances compared to pristine ZnO NWs. ZnO:Ag nanowire/nanorod arrays electrochemically grown on p-type GaN single crystal layer is also shown to act as light emitter in LED structures. The emission wavelength is red-shifted compared to pristine ZnO NW array. At low Ag concentration a single UV-blue emission is found whereas at higher concentration of dopant the emission is broadened and extends up to the red wavelength range. Our study indicates that high quality ZnO:Ag NW/NR prepared at low temperature by electrodeposition can serve as building nanomaterials for new sensors and light emitting diodes (LEDs) structures with low-power consumption.

  7. Ag-nanoparticle-decorated porous ZnO-nanosheets grafted on a carbon fiber cloth as effective SERS substrates.

    PubMed

    Wang, Zhiwei; Meng, Guowen; Huang, Zhulin; Li, Zhongbo; Zhou, Qitao

    2014-12-21

    We report on the large-scale synthesis of Ag-nanoparticle (Ag-NP) decorated ZnO-mesoporous-nanosheets (NSs) grafted on a flexible carbon fiber cloth (CFC), as sensitive and reproducible surface enhanced Raman scattering (SERS) substrates with excellent flexibility. The composite SERS-substrates are achieved by a combination of atomic layer deposition of ZnO-seeds on each fiber of the CFC (denoted as ZnO-seeds@CFC), chemical bath deposition and subsequent pyrolysis for the creation of ZnO-mesoporous-NSs grafted on ZnO-seeds@CFC, and ion-sputtering of Ag-NPs on the ZnO-mesoporous-NSs. As abundant SERS "hot spots" are generated from the electromagnetic coupling of the densely distributed Ag-NPs, and the semiconducting ZnO-mesoporous-NSs also have chemical supporting enhancement and distinct molecule adsorbing abilities, the composite SERS-substrates demonstrate high SERS-sensitivity with good signal reproducibility. As a trial for potential applications, the composite SERS-substrates were used to identify pesticides and highly toxic polychlorinated biphenyls (PCBs), and low concentrations down to 10(-7) M for methyl parathion and 5 × 10(-6) M for PCB-77 were reached, respectively, showing promising potential for the SERS-based rapid detection of toxic organic pollutants in the environment.

  8. Influence of Fluoride Ion on the Performance of Pb-Ag Anode During Long-Term Galvanostatic Electrolysis

    NASA Astrophysics Data System (ADS)

    Zhong, Xiaocong; Yu, Xiaoying; Jiang, Liangxing; Lv, Xiaojun; Liu, Fangyang; Lai, Yanqing; Li, Jie

    2015-09-01

    Anodic potential, morphology and phase composition of the anodic layer, corrosion morphology of the metallic substrate, and oxygen evolution behavior of Pb-Ag anode in H2SO4 solution without/with fluoride ion were investigated and compared. The results showed that the presence of fluoride ions contributed to a smoother anodic layer with lower PbO2 concentration, which resulted in lower double layer capacity and higher charge transfer resistance for the oxygen evolution reaction. Consequently, the Pb-Ag anode showed a higher anodic potential (about 35 mV) in the fluoride-containing electrolyte. In addition, the fluoride ions accelerated the detachment of loose flakes on the anodic layer. It was demonstrated that the anodic layer formed in the fluoride-containing H2SO4 solution was thinner. Furthermore, fluoride ions aggravated the corrosion of the metallic substrate at interdendritic boundary regions. Hence, the presence of fluoride ions is detrimental to oxygen evolution reactivity and increases the corrosion of the Pb-Ag anode, which may further increase the energy consumption and capital cost of zinc plants.

  9. The simple hydrothermal synthesis of Ag-ZnO-SnO2 nanochain and its multiple applications.

    PubMed

    Balachandran, Subramanian; Selvam, Kaliyamoorthy; Babu, Balraj; Swaminathan, Meenakshisundaram

    2013-12-14

    In this article, we report the fabrication of a stable Ag-ZnO-SnO2 nanochain by template free hydrothermal method and its photocatalytic activity for the first time. This composite material represents a potential new class of photocatalysts with enhanced light absorption, hydrophobic and electronic properties of ZnO. This catalyst has been characterized by X-ray diffraction (XRD), high resolution scanning electron microscopy (HRSEM), field emission scanning electron microscopy (FESEM), elemental mapping, energy dispersive spectroscopy (EDS), X-ray photoelectron spectroscopy (XPS), UV-Vis diffuse reflectance spectroscopy (DRS) and photoluminescence spectroscopy (PL). XRD and elemental mapping reveal the presence of SnO2 and Ag in the catalyst. Ag-ZnO-SnO2 has increased absorption in the visible region when compared to ZnO. This three component nano junction system exhibits enhanced photocatalytic activity for the degradation of azo dyes, Acid Black 1 (AB 1) and Acid Violet 7 (AV 7) under UV light (365 nm), far exceeding those of the single and two component systems. Ag-ZnO-SnO2 is found to be reusable without appreciable loss of catalytic activity up to four runs. Based on the band gap energies of ZnO and SnO2, a mechanism is proposed for the photodegradation of dyes. Hydrophobicity and photoconductivity of Ag-ZnO-SnO2 have been evaluated. Nanochain exhibiting higher positive photoconductivity can be useful for soliton wave communication as well as solar cell applications. Our results provide some new insights on the fabrication of Ag-ZnO-SnO2 and its performance as an active photocatalyst, self cleaning and conducting material.

  10. Boron-rich mud volcanoes of the Black Sea region: modern analogues to ancient sea-floor tourmalinites associated with Sullivan-type Pb-Zn deposits?

    USGS Publications Warehouse

    Slack, J.F.; Turner, R.J.W.; Ware, P.L.G.

    1998-01-01

    Large submarine mud volcanoes in the abyssal part of the Black Sea south of the Crimean Peninsula are similar in many respects to synsedimentary mud volcanoes in the Mesoproterozoic Belt-Purcell basin. One of the Belt-Purcell mud volcanoes directly underlies the giant Sullivan Pb-Zn-Ag deposit in southeastern British Columbia. Footwall rocks to the Sullivan deposit comprise variably tourmalinized siltstone, conglomerate, and related fragmental rock; local thin pyrrhotite-rich and spessartine-quartz beds are interpreted as Fe and Fe-Mn exhalites, respectively. Analogous Fe- and Mn-rich sediments occur near the abyssal Black Sea mud volcanoes. Massive pyrite crusts and associated carbonate chimneys discovered in relatively shallow waters (~200 m depth) west of the Crimean Peninsula indicate an active sea-floor-hydrothermal system. Subaerial mud volcanoes on the Kerch and Taman Peninsulas (~100 km north of the abyssal mud volcanoes) contain saline thermal waters that locally have very high B contents (to 915 mg/L). These data suggest that tourmalinites might be forming in or near submarine Black Sea mud volcanoes, where potential may also exist for Sullivan-type Pb-Zn mineralization.

  11. ZnO-Ag core shell nanocomposite formed by green method using essential oil of wild ginger and their bactericidal and cytotoxic effects

    NASA Astrophysics Data System (ADS)

    Azizi, Susan; Mohamad, Rosfarizan; Rahim, Raha Abdul; Moghaddam, Amin Boroumand; Moniri, Mona; Ariff, Arbakariya; Saad, Wan Zuhainis; Namvab, Farideh

    2016-10-01

    In this paper, a novel green method for fabrication of zinc oxide-silver (ZnO-Ag) core-shell nanocomposite using essential oil of ginger (EO-G) is reported. The EO-G played two significant roles in the synthesis process: it could act as a reaction media for the formation of ZnO and reduce Ag+ to Ag0. The bioformed ZnO-Ag nanocomposite was compared with pure biosynthesized ZnO-NPs and characterized by UV-vis spectroscopy, TEM, EDX, XRD and FTIR. The characterization results confirmed that Ag-NPs had been embedded in ZnO hexagonal nanoparticles. Six Gram positive and negative pathogens were used to investigate the antibacterial effects of these samples. Ag-doping improves the bactericidal activity of ZnO-NPs. In vitro cytotoxicity studies on Vero cells, a dose dependent toxicity with non-toxic effect of concentration below 100 μg/mL was shown for ZnO-Ag nanocomposite. The biosynthesized ZnO-Ag nanocomposites were found to be comparable to those obtained from the conventional methods using hazardous materials which can be an excellent alternative for the synthesis of ZnO-Ag using biomass.

  12. SERS-active ZnO/Ag hybrid WGM microcavity for ultrasensitive dopamine detection

    NASA Astrophysics Data System (ADS)

    Lu, Junfeng; Xu, Chunxiang; Nan, Haiyan; Zhu, Qiuxiang; Qin, Feifei; Manohari, A. Gowri; Wei, Ming; Zhu, Zhu; Shi, Zengliang; Ni, Zhenhua

    2016-08-01

    Dopamine (DA) is a potential neuro modulator in the brain which influences a variety of motivated behaviors and plays a key role in life science. A hybrid ZnO/Ag microcavity based on Whispering Gallery Mode (WGM) effect has been developed for ultrasensitive detection of dopamine. Utilizing this effect of structural cavity mode, a Raman signal of R6G (5 × 10-3 M) detected by this designed surface-enhanced Raman spectroscopy (SERS)-active substrate was enhanced more than 10-fold compared with that of ZnO film/Ag substrate. Also, this hybrid microcavity substrate manifests high SERS sensitivity to rhodamine 6 G and detection limit as low as 10-12 M to DA. The Localized Surface Plasmons of Ag nanoparticles and WGM-enhanced light-matter interaction mainly contribute to the high SERS sensitivity and help to achieve a lower detection limit. This designed SERS-active substrate based on the WGM effect has the potential for detecting neurotransmitters in life science.

  13. Transparent capacitors with hybrid ZnO:Al and Ag nanowires as electrodes.

    PubMed

    Zhang, Guozhen; Wu, Hao; Wang, Xiao; Wang, Ti; Liu, Chang

    2016-03-11

    Transparent conducting films with a composite structure of AlZnO-Ag nanowires (AgNWs) have been prepared by atomic layer deposition. The sheet resistance was reduced from 120 to 9 Ω when the AgNW networks were involved. Transparent capacitors with Al2O3-TiO2-Al2O3 dielectrics were fabricated on the composite electrodes and demonstrated a capacitance density of 10.1 fF μm(-2), which was significantly higher than that of capacitors with AlZnO electrodes (8.8 fF μm(-1)). The capacitance density remained almost unchanged in a broad frequency range from 3 kHz to 1 MHz. Moreover, a low leakage current density of 2.4 × 10(-7) A cm(-2) at 1 V was achieved. Transparent and flexible capacitors were also fabricated using the composite electrodes, and demonstrated an improved bendability. The transparent capacitors showed an average optical transmittance over 70% in the visible range, and thus open the door to practical applications in transparent integrated circuits.

  14. Ag/ZnO nanomaterials as high performance sensors for flammable and toxic gases.

    PubMed

    Simon, Quentin; Barreca, Davide; Gasparotto, Alberto; Maccato, Chiara; Tondello, Eugenio; Sada, Cinzia; Comini, Elisabetta; Devi, Anjana; Fischer, Roland A

    2012-01-20

    Ag/ZnO nanocomposites supported on polycrystalline Al2O3 were synthesized by an unprecedented approach combining plasma enhanced chemical vapor deposition (PE-CVD) of ZnO matrices and the subsequent deposition of Ag nanoparticles (NPs) by radio frequency (RF) sputtering. The system structure, composition and morphology were investigated by glancing incidence x-ray diffraction (GIXRD), secondary ion mass spectrometry (SIMS), field emission scanning electron microscopy (FE-SEM) and energy dispersive x-ray spectroscopy (EDXS). A tailored dispersion and distribution of silver particles could be obtained under mild conditions by the sole variation of the sputtering time. Gas sensing properties toward flammable and toxic gases, both reducing (CH3CH2OH, CH3COCH3) and oxidizing (O3), were investigated in the temperature range 100-400 °C. Beside the high sensitivity, the developed sensors exhibited a response proportional to Ag content, thanks to catalytic and electronic effects promoted by silver NPs. In addition, discrimination between oxidizing and reducing analytes was enabled by a suitable choice of the adopted working temperature.

  15. Effects of crucible wetting during solidification of immiscible Pb-Zn

    NASA Technical Reports Server (NTRS)

    Degroh, Henry C., III; Probst, Hubert B.

    1988-01-01

    Many industrial uses for liquid phase miscibility gap alloys are proposed. However, the commercial production of these alloys into useful ingots with a reasonable amount of homogeneity is arduous because of their immiscibility in the liquid state. In the low-g environment of space gravitational settling forces are abated, thus solidification of an immiscible alloys with a uniform distribution of phases becomes feasible. Elimination of gravitational settling and coalescence processes in low-g also makes possible the study of other separation and coarsening mechanisms. Even with gravitational separation forces reduced, many low-g experiments have resulted in severely segregated structures. The segregation in many cases was due to preferential wetting of the crucible by one of the immiscible liquids. The objective was to analyze the wetting behavior of Pb-Zn alloys on various crucible materials in an effort to identify a crucible in which the fluid flow induced by preferential wetting is minimized. It is proposed that by choosing the crucible for a particular alloy so that the difference in surface energy between the solid and two liqud phases is minimized, the effects of preferential wetting can be diminished and possibly avoided. Qualitative experiments were conducted and have shown the competitive wetting behavior of the immiscible Pb-Zn system and 13 different crucible materials.

  16. Effects of crucible wetting during solidification of immiscible Pb-Zn alloys

    NASA Technical Reports Server (NTRS)

    De Groh, H. C., III; Probst, H. B.

    1989-01-01

    Many industrial uses for liquid phase miscibility gap alloys are proposed. However, the commercial production of these alloys into useful ingots with a reasonable amount of homogeneity is arduous because of their immiscibility in the liquid state. In the low-g environment of space gravitational settling forces are abated, thus solidification of an immiscible alloy with a uniform distribution of phases becomes feasible. Elimination of gravitational settling and coalescence processes in low-g also makes possible the study of other separation and coarsening mechanisms. Even with gravitational separation forces reduced, many low-g experiments have resulted in severely segregated structures. The segregation in many cases was due to preferential wetting of the crucible by one of the immiscible liquids. The objective was to analyze the wetting behavior of Pb-Zn alloys on various crucible materials in an effort to identify a crucible in which the fluid flow induced by preferential wetting is minimized. It is proposed that by choosing the crucible for a particular alloy so that the difference in surface energy between the solid and two liquid phases is minimized, the effects of preferential wetting can be diminished and possibly avoided. Qualitative experiments were conducted and have shown the competitive wetting behavior of the immiscible Pb-Zn system and 13 different crucible materials.

  17. Selenium in soils, spermatophytes and bryophytes around a Zn-Pb smelter, New South Wales, Australia.

    PubMed

    Huang, Yi Jian; Gulson, Brian L

    2002-07-01

    Selenium concentrations and its spatial distribution in soils, spermatophytes and bryophytes (mosses) around the Cockle Creek Zn-Pb smelter, New South Wales were studied from May to November 2000. Selenium was determined by ICP-MS on soils digested in nitric and hydrochloric acid (HNO3:HCl = 3:1), and plant samples digested in distilled concentrated nitric acid. At distances greater than 3 km, selenium in soils, spermatophytes and bryophytes converge to uniform values, which are considered to represent the background value. Mean selenium in soils around the smelter is two times higher than the background value. Mean concentration of selenium in plants around the smelter is three times greater than that for background plants. Selenium from 'in site' bryophyte is twice that found in the background bryophyte. The transfer coefficients of selenium between plants and soils are low, especially at a distance less than 1 km from the smelter. However, mosses show the reverse trend. This study indicates that the Zn-Pb smelter is one of the anthropogenic point sources of selenium pollution in the Lake Macquarie district.

  18. Heavy metal (Cd, Pb, Zn) and metalloid (As) content in raptor species from Galicia (NW Spain).

    PubMed

    Pérez-López, Marcos; Hermoso de Mendoza, María; López Beceiro, Ana; Soler Rodríguez, Francisco

    2008-05-01

    As top consumers in food chains, birds of prey forage over large geographical areas and so might be expected to accumulate environmental contaminants which are distributed in the environment. These wild animals can offer opportunities to detect and assess the toxicological effects of different inorganic elements on terrestrial ecosystems. In this study, different raptor species, both diurnal and nocturnal, were investigated for heavy metal (Pb, Cd and Zn) and As concentrations in liver samples, with the aim of furnishing indirect information concerning contamination of their habitats. Dead animals were obtained with the special collaboration of the Wildlife Rehabilitation Centres from Galicia (NW Spain). After sample wet digestion, metal analysis was performed by inductively coupled plasma-mass spectrometry (ICP-MS). Hepatic concentrations of Zn and As, respectively, situated on the interval 147-298 and 1.21-6.88 ppm (dry weight, dw), could be considered as indicative of low and background amounts of both elements, with no ecotoxicological concern. Nevertheless, with respect to Pb, some diurnal raptors showed hepatic concentrations above the considered threshold value (6 ppm dw) for sublethal or lethal toxicity, the species with the highest hepatic level corresponding to a common buzzard (>18 ppm, dw). Similarly, nocturnal raptors exceeded the threshold value for Cd (3 ppm dw), with a maximum corresponding to an individual barn owl (39 ppm, dw). In both cases, although concentrations could not be directly related to lethal effect, they might constitute a serious environmental factor affecting the survival of the considered populations. PMID:17617459

  19. Synthesis and Characterization of Varying Concentrations of Ag-doped ZnO Thin Films

    NASA Astrophysics Data System (ADS)

    Hachlica, Justin; Wadie-Ibrahim, Patrick; Sahiner, M. Alper

    Silver doped ZnO is a promising compound for photovoltaic solar cell use. Doping this compound with varying amounts of silver will theoretically make this type of thin film more efficient by reducing the overall resistance and increasing the voltage and current output. The extent of this promise is being tested experimentally, by analysis of both the electrical and the surface roughness properties of the cells. Ag-doped Zinc Oxide is deposited by method of Pulsed Laser Deposition (PLD) onto Indium Tin Oxide (ITO) coated Glass. Annealing effects were also observed by varying the temperature at which the annealing occurred after synthesis of the sample. Thickness is confirmed by use of Ellipsometery. X-Ray Diffraction (XRD) measurements confirmed a ZnO crystal structure on the thin films. The active dopant carrier concentrations were determined using a Hall Effect Measuring System. Finally, the photovoltaic properties of the film are recorded by using a Keithley Source Meter. The structural characterization and electrical results of the effect of Ag doping on ZnO will then be discussed.

  20. Pollution of montane soil with Cu, Zn, As, Sb, Pb, and nitrate in Kanto, Japan.

    PubMed

    Takamatsu, Takejiro; Watanabe, Mirai; Koshikawa, Masami K; Murata, Tomoyoshi; Yamamura, Shigeki; Hayashi, Seiji

    2010-03-15

    Soil cores and rainwater were sampled under canopies of Cryptomeria japonica in four montane areas along an atmospheric depositional gradient in Kanto, Japan. Soil cores (30cm in depth) were divided into 2-cm or 4-cm segments for analysis. Vertical distributions of elemental enrichment ratios in soils were calculated as follows: (X/Al)(i)/(X/Al)(BG) (where the numerator and denominator are concentration ratios of element-X and Al in the i- and bottom segments of soil cores, respectively). The upper 14-cm soil layer showed higher levels of Cu, Zn, As, Sb, and Pb than the lower (14-30cm) soil layer. In the four areas, the average enrichment ratios in the upper 6-cm soil layer were as follows: Pb (4.93)>or=Sb (4.06)>or=As (3.04)>Zn (1.71)>or=Cu (1.56). Exogenous elements (kg/ha) accumulated in the upper 14-cm soil layer were as follows: Zn (26.0)>Pb (12.4)>Cu (4.48)>or=As (3.43)>or=Sb (0.49). These rank orders were consistent with those of elements in anthropogenic aerosols and polluted (roadside) air, respectively, indicating that air pollutants probably caused enrichment of these elements in the soil surface layer. Approximately half of the total concentrations of As, Sb, and Pb in the upper 14-cm soil layer were derived from exogenous (anthropogenic) sources. Sb showed the highest enrichment factor in anthropogenic aerosols, and shows similar deposition behavior to NO(3)(-), which is a typical acidic air pollutant. There was a strong correlation between Sb and NO(3)(-) concentrations in rainfall (e.g., in the throughfall under C. japonica: [NO(3)(-)]=21.1 [dissolved Sb], r=0.938, p<0.0001, n=182). Using this correlation, total (cumulative) inputs of NO(3)(-) were estimated from the accumulated amounts of exogenous Sb in soils, i.e., 16.7t/ha at Mt. Kinsyo (most polluted), 8.6t/ha at Mt. Tsukuba (moderately polluted), and 5.8t/ha at the Taga mountain system (least polluted). There are no visible ecological effects of these accumulated elements in the Kanto region at

  1. Sublethal mechanisms of Pb and Zn toxicity to the purple sea urchin (Strongylocentrotus purpuratus) during early development.

    PubMed

    Tellis, Margaret S; Lauer, Mariana M; Nadella, Sunita; Bianchini, Adalto; Wood, Chris M

    2014-01-01

    In order to understand sublethal mechanisms of lead (Pb) and zinc (Zn) toxicity, developing sea urchins were exposed continuously from 3h post-fertilization (eggs) to 96 h (pluteus larvae) to 55 (±2.4) μgPb/L or 117 (±11)μgZn/L, representing ~ 70% of the EC50 for normal 72 h development. Growth, unidirectional Ca uptake rates, whole body ion concentrations (Na, K, Ca, Mg), Ca(2+) ATPase activity, and metal bioaccumulation were monitored every 12h over this period. Pb exhibited marked bioaccumulation whereas Zn was well-regulated, and both metals had little effect on growth, measured as larval dry weight, or on Na, K, or Mg concentrations. Unidirectional Ca uptake rates (measured by (45)Ca incorporation) were severely inhibited by both metals, resulting in lower levels of whole body Ca accumulation. The greatest disruption occurred at gastrulation. Ca(2+) ATPase activity was also significantly inhibited by Zn but not by Pb. Interestingly, embryos exposed to Pb showed some capacity for recovery, as Ca(2+)ATPase activities increased, Ca uptake rates returned to normal intermittently, and whole body Ca levels were restored to control values by 72-96 h of development. This did not occur with Zn exposure. Both Pb and Zn rendered their toxic effects through disruption of Ca homeostasis, though likely through different proximate mechanisms. We recommend studying the toxicity of these contaminants periodically throughout development as an effective way to detect sublethal effects, which may not be displayed at the traditional toxicity test endpoint of 72 h. PMID:24326189

  2. Re-Os pyrite geochronology of Zn-Pb mineralization in the giant Caixiashan deposit, NW China

    NASA Astrophysics Data System (ADS)

    Li, Dengfeng; Chen, Huayong; Hollings, Pete; Zhang, Li; Mi, Mei; Li, Jie; Fang, Jing; Wang, Chengming; Lu, Wanjian

    2016-03-01

    The newly discovered Caixiashan Irish-type Zn-Pb deposit (˜131 Mt at 3.95 % Zn + Pb), located in the Eastern Tianshan of Xinjiang, is one of the largest Zn-Pb deposits in NW China. Massive colloform/framboidal textured syn-sedimentary pyrite yielded a Re-Os isochron age of 1019 ± 70 Ma (MSWD = 3.5), which is interpreted to be the depositional age of the Kawabulake group that hosts the ore. The age of the main mineralization stage is constrained by two types of pyrite: the layered pyrite coexists with recrystallized calcite and dolomite and is locally replaced by sphalerite, whereas the euhedral pyrite occurs with galena that crosscuts the massive sphalerite. The layered pyrite yielded a Re-Os age of 859 ± 79 Ma (MSWD = 6.7; initial 187Os/188Os ratio [IOs] = 0.19 ± 0.25) and the euhedral pyrite 837 ± 39 Ma (MSWD = 6.5; [IOs] = 0.16 ± 0.09), which are interpreted to be the Zn and Pb mineralization ages, respectively. The low radiogenic initial Os values of the Zn-Pb mineralization suggest interaction between a hydrothermal fluid and a mafic or ultramafic source rock with a mantle Os signature with some contamination with Mesoproterozoic Kawabulake group. Based on our new Re-Os ages, we conclude that the giant Caixiashan Zn-Pb deposit formed in the early Neoproterozoic and it represents a newly identified mineralization epoch in the Eastern Tianshan of the Central Asia Orogenic Belt.

  3. Long-term changes of metal contents in two metallophyte species (Olkusz area of Zn-Pb ores, Poland).

    PubMed

    Kicińska, Alicja; Gruszecka-Kosowska, Agnieszka

    2016-06-01

    The authors present the changes of the As, Cd, Fe, Mn, Pb and Zn contents in two plant-considered metallophytes: common bent Agrostis capillaris (blades) and birch Betula pendula (leaves and seeds), recorded in a Zn-Pb industrial region of Olkusz (Poland) in 1994 and 2014. The highest amounts of Cd (12 ppm) and Zn (2524 ppm) in the common bent occur in the vicinity of the mining and metallurgical works 'Bolesław' in Bukowno. However, these values are significantly lower than those in 1994: Cd by 87 % and Zn by 52 %. The highest contents of Fe (2674 ppm), Mn (130 ppm) and Pb (334 ppm) in this grass species are in the vicinity of the closed Olkusz mine. These contents have increased in comparison with the 1994 figures: Fe by 56 %, Mn by 120 % and Pb by 6 %. In the birch leaves, the metal contents averaged for four sites are the following: As 2.1, Cd 6.5, Fe 261, Mn 110, Pb 70 and Zn 1657 ppm, being lower from the figures in 1994. The highest As, Fe and Pb contents of birch leaves occur in the habitat closest to the former Olkusz mine, while those of Cd, Mn and Zn in the habitat distant at 100 m from the active plant in Bukowno. The common bent grass generates better resistance mechanisms against the metals than does the birch. In the birch leaves, the contents of the metals are significantly lower than those of the grass blades, but higher from those of the birch seeds collected from the same tree individuals. It is a proof of good functioning of the mechanisms preventing excessive metal amounts from the cell metabolism and of the presence of physiological barriers protecting birch seeds as the generative organs. PMID:27165603

  4. Cation Exchange Selectivity versus concentration of competing heavy metal cations (Pb2+,Zn2+) : case of Na-montmorillonite

    NASA Astrophysics Data System (ADS)

    Oueslati, W.; Mefath, M.; Ben Rhaiem, H.; Ben Haj Amara, A.

    2009-11-01

    Cation Exchange Selectivity (CES) for Wyoming montmorillonite was determined by equilibration of the clay with a mixed equinormal solution containing two competing cations (i.e. Pb2+, Zn2+). This paper aims at characterizing the structural change and selectivity of a Na-dioctahedral smectite (Wy-Na). The quantitative analysis of XRD patterns is achieved using an indirect method based on the comparison of XRD experimental patterns to calculated ones. Two reference samples were prepared by saturation with Pb2+ or Zn2+ (i.e. two heavy metal cations occurring in hold house trash). The resulting complexes were respectively labelled Wy-Pb and Wy-Zn. After that, the Wy-Na sample was dispersed in solutions containing 0.5Pb2+ and 0.5Zn2+ with different concentrations (from 10-2 N to 10-4 N) in order to understand the concentration effect on the selectivity process of the Na-montmorillonite. The XRD quantitative analysis shows that for low concentrations the d001 spacing value corresponds to Wy-Na complex, whereas for high concentrations the d001 spacing value can be attributed to the Wy-Zn and/or Wy-Pb. At low concentrations, the sample presents a homogeneous state and the cation exchange capacity is saturated with Na+ cation which is characterized by one water layer hydration state (1W). For high concentrations, interstratified hydration behavior appears and the clay has a tendency to exchange in minor contribution the Zn2+ cation and in major contribution Pb2+ cation characterized by a mixed hydration state between one (1W) and two water layers (2W).

  5. Thermal Expansion and Second Harmonic Generation Response of the Tungsten Bronze Pb2AgNb5O15.

    PubMed

    Lin, Kun; Gong, Pifu; Sun, Jing; Ma, Hongqiang; Wang, You; You, Li; Deng, Jinxia; Chen, Jun; Lin, Zheshuai; Kato, Kenichi; Wu, Hui; Huang, Qingzhen; Xing, Xianran

    2016-03-21

    The incorporation of transition metal element Ag was performed to explore negative thermal expansion (NTE) materials with tetragonal tungsten bronze (TTB) structures. In this study, the structure and thermal expansion behaviors of a polar TTB oxide, Pb2AgNb5O15 (PAN), were systematically investigated by high-resolution synchrotron powder diffraction, high-resolution neutron powder diffraction, transmission electron microscope (TEM), and high-temperature X-ray diffractions. The TEM and Rietveld refinements revealed that the compound PAN displays (√2a(TTB), √2b(TTB), 2c(TTB))-type superstructure. This superstructure within the a-b plane is caused by the ordering of A-site cations, while the doubling of the c axis is mainly induced by a slight tilt distortion of the NbO6 octahedra. The transition metal Ag has larger spontaneous polarization displacements than Pb, but the Pb-O covalence seems to be weakened compared to the potassium counterpart Pb2KNb5O15 (PKN), which may account for the similar Curie temperature and uniaxial NTE behavior for PAN and PKN. Powder second harmonic generation (SHG) measurement indicates that PAN displays a moderate SHG response of ∼0.2 × LiNbO3 (or ∼100 × α-SiO2) under 1064 nm laser radiation. The magnitudes of the local dipole moments in NbO6 and PbOx polyhedra were quantified using bond-valence approach. We show that the SHG response stems from the superposition of dipole moments of both the PbO(x) and NbO6 polyhedra.

  6. Thermal Expansion and Second Harmonic Generation Response of the Tungsten Bronze Pb2AgNb5O15.

    PubMed

    Lin, Kun; Gong, Pifu; Sun, Jing; Ma, Hongqiang; Wang, You; You, Li; Deng, Jinxia; Chen, Jun; Lin, Zheshuai; Kato, Kenichi; Wu, Hui; Huang, Qingzhen; Xing, Xianran

    2016-03-21

    The incorporation of transition metal element Ag was performed to explore negative thermal expansion (NTE) materials with tetragonal tungsten bronze (TTB) structures. In this study, the structure and thermal expansion behaviors of a polar TTB oxide, Pb2AgNb5O15 (PAN), were systematically investigated by high-resolution synchrotron powder diffraction, high-resolution neutron powder diffraction, transmission electron microscope (TEM), and high-temperature X-ray diffractions. The TEM and Rietveld refinements revealed that the compound PAN displays (√2a(TTB), √2b(TTB), 2c(TTB))-type superstructure. This superstructure within the a-b plane is caused by the ordering of A-site cations, while the doubling of the c axis is mainly induced by a slight tilt distortion of the NbO6 octahedra. The transition metal Ag has larger spontaneous polarization displacements than Pb, but the Pb-O covalence seems to be weakened compared to the potassium counterpart Pb2KNb5O15 (PKN), which may account for the similar Curie temperature and uniaxial NTE behavior for PAN and PKN. Powder second harmonic generation (SHG) measurement indicates that PAN displays a moderate SHG response of ∼0.2 × LiNbO3 (or ∼100 × α-SiO2) under 1064 nm laser radiation. The magnitudes of the local dipole moments in NbO6 and PbOx polyhedra were quantified using bond-valence approach. We show that the SHG response stems from the superposition of dipole moments of both the PbO(x) and NbO6 polyhedra. PMID:26928907

  7. Pb, Cu, and Zn distributions at humic acid-coated metal-oxide surfaces

    DOE PAGES

    Wang, Yingge; Michel, F. Marc; Choi, Yongseong; Eng, Peter J.; Levard, Clement; Siebner, Hagar; Gu, Baohua; Bargar, John R.; Brown, Gordon E.

    2016-05-09

    Here, mineral surfaces are often coated by natural organic matter (NOM), which has a major influence on metal-ion sorption and sequestration because of the abundance of binding sites in such coatings and the changes they cause in local nanoscale environments. The effects of NOM coatings on mineral surfaces are, however, still poorly understood at the molecular level due to the complexity of these systems. In this study, we have applied long-period X-ray standing wave-fluorescence yield (LP-XSW-FY) spectroscopy to measure the partitioning of naturally present Cu(II) (0.0226%), Zn(II) (0.009%), and Pb(II) ( 0.0004%) between Elliott Soil Humic Acid (ESHA) coatings andmore » three model single-crystal metal-oxide substrates: α-Al2O3 (0 0 0 1), α-Al2O3 (1 1 0 2), and α-Fe2O3 (0 0 0 1). The competitive sorption effects among these metal ions for binding sites in the ESHA coatings and on the metal-oxide surfaces were investigated as a function of reaction time, calcium content, and solution pH. Pb(II) ions present in the ESHA coatings were found to redistribute to reactive α-Al2O3 (1 1 0 2) and α-Fe2O3 (0 0 0 1) surfaces after 3 h of reaction (pH = 6.0, [Ca(II)] = 2 mM). Pb(II) partitioning onto these reactive metal-oxide surfaces increased with increasing reaction time (up to 7 d). In addition, the partitioning of Cu(II) and Zn(II) from the ESHA coating to the α-Fe2O3 (0 0 0 1) substrate increased slightly with reaction time (2.4% and 3.7% for Cu(II) and Zn(II), respectively, after 3 h and 6.4% and 7.7% for Cu(II) and Zn(II), respectively, after 72 h of reaction time).« less

  8. Stabilization of As, Cr, Cu, Pb and Zn in soil using amendments--a review.

    PubMed

    Kumpiene, Jurate; Lagerkvist, Anders; Maurice, Christian

    2008-01-01

    The spread of contaminants in soil can be hindered by the soil stabilization technique. Contaminant immobilizing amendments decrease trace element leaching and their bioavailability by inducing various sorption processes: adsorption to mineral surfaces, formation of stable complexes with organic ligands, surface precipitation and ion exchange. Precipitation as salts and co-precipitation can also contribute to reducing contaminant mobility. The technique can be used in in situ and ex situ applications to reclaim and re-vegetate industrially devastated areas and mine-spoils, improve soil quality and reduce contaminant mobility by stabilizing agents and a beneficial use of industrial by-products. This study is an overview of data published during the last five years on the immobilization of one metalloid, As, and four heavy metals, Cr, Cu, Pb and Zn, in soils. The most extensively studied amendments for As immobilization are Fe containing materials. The immobilization of As occurs through adsorption on Fe oxides by replacing the surface hydroxyl groups with the As ions, as well as by the formation of amorphous Fe(III) arsenates and/or insoluble secondary oxidation minerals. Cr stabilization mainly deals with Cr reduction from its toxic and mobile hexavalent form Cr(VI) to stable in natural environments Cr(III). The reduction is accelerated in soil by the presence of organic matter and divalent iron. Clays, carbonates, phosphates and Fe oxides were the common amendments tested for Cu immobilization. The suggested mechanisms of Cu retention were precipitation of Cu carbonates and oxy-hydroxides, ion exchange and formation of ternary cation-anion complexes on the surface of Fe and Al oxy-hydroxides. Most of the studies on Pb stabilization were performed using various phosphorus-containing amendments, which reduce the Pb mobility by ionic exchange and precipitation of pyromorphite-type minerals. Zn can be successfully immobilized in soil by phosphorus amendments and clays.

  9. Interaction of Cu(2+), Pb (2+), Zn (2+) with trypsin: what is the key factor of their toxicity?

    PubMed

    Zhang, Tong; Zhang, Hao; Liu, Guiliang; Gao, Canzhu; Liu, Rutao

    2014-11-01

    Heavy metals possess great endangerment to environment even human health because of their indissolubility and bioaccumulation. The toxicity of heavy metal ions (Cu(2+), Pb(2+), Zn(2+)) to trypsin was investigated by fluorescence, synchronous fluorescence, UV-vis absorption, circular dichroism (CD) spectroscopy, isothermal titration calorimetry (ITC), and enzyme activity assay. The experimental results showed that toxic effect of heavy metal ions was due to their own characteristic, rather than the electric charges of the ion. Zn(2+) could not show the obvious toxicity to trypsin, while the structure and function of trypsin was damaged when the enzyme explored to Cu(2+) and Pb(2+). From the spectra results, we found that Cu(2+) would bind with trypsin, which lead to the fluorescence quenched and hydrophobicity increased. Pb(2+) could also change the structure and reduce the activity of trypsin in high concentration. In vitro measurement, the toxicity order of heavy metal ions to trypsin is: Cu(2+) > Pb(2+) > Zn(2+). In addition, isothermal titration calorimetry analysis proved that the interactions between Cu(2+), Pb(2+), Zn(2+) and trypsin were all spontaneous and exothermic, which indicated the adverse effect of these heavy metal ions to trypsin. PMID:25323557

  10. Cu-Zn-Pb multi isotopic characterization of a small watershed (Loire river basin, France)

    NASA Astrophysics Data System (ADS)

    Desaulty, A. M.; Millot, R.; Perret, S.; Bourrain, X.

    2015-12-01

    Combating metal pollution in surface water is a major environmental, public health and economic issue. Knowledge of the behavior of metals, such as copper (Cu), zinc (Zn) and lead (Pb) in sediments and dissolved load, is a key factor to improve the management of rivers. Recent advances in mass spectrometry related to the development of MC-ICPMS allow to analyze the isotopic composition of these elements, and previous studies show the effectiveness of isotopic analyses to determine the anthropogenic sources of pollution in environment. The goal of this study is to use the Cu-Zn-Pb multi-isotopic signature to track the pollutions in surface water, and to understand the complex processes causing the metals mobilization and transport in environment. More particularly we investigate the mechanisms of distribution between the dissolved load and particulate load, known to play an important role in the transport of metals through river systems. As case study, we chose a small watershed, poorly urbanized in the Loire river basin. Its spring is in a pristine area, while it is only impacted some kilometers further by the releases rich in metals coming from a hospital water treatment plant. First a sampling of these liquid effluents as well as dissolved load and sediment from upstream to downstream was realized and their concentrations and isotopic data were determined. Then to simulate a lot of potential natural and anthropogenic modifications of environmental conditions, we made sequential extraction protocol using various reagents on the sediments. Isotopic analyzes were performed also on the various extracting solutions. Isotopic ratios were measured using a Neptune MC-ICPMS at the BRGM, after a protocol of purification for Zn and Cu. The results showed that, these isotopic systematics reveal important informations about the mechanists of mobilization and transport of metals through river systems. However experiments performed under laboratory conditions will be necessary

  11. The world-class Howard's Pass SEDEX Zn-Pb district, Selwyn Basin, Yukon. Part I: trace element compositions of pyrite record input of hydrothermal, diagenetic, and metamorphic fluids to mineralization

    NASA Astrophysics Data System (ADS)

    Gadd, Michael G.; Layton-Matthews, Daniel; Peter, Jan M.; Paradis, Suzanne J.

    2016-03-01

    The Howard's Pass district, located in Yukon Territory, comprises 14 Zn-Pb sedimentary exhalative (SEDEX) deposits that collectively contain approximately 400.7 Mt grading at 4.5 % Zn and 1.5 % Pb. Sulfide mineralization is hosted in carbonaceous and calcareous to siliceous mudstones. Pyrite is a minor but ubiquitous component. Detailed petrographic analyses reveal that pyrite has a complex and protracted growth history, and multiple generations of pyrite are preserved in single grains. Combined electron probe microanalysis (EPMA) and laser ablation-inductively coupled mass plasma-mass spectrometry (LA-ICP-MS) of paragenetically complex pyrite reveal minor and trace element zonation that mimic textural features. These data provide information on the relative timing and cation content of depositional (i.e., ambient marine), hydrothermal, and metamorphic fluids. These data also identify a suite of nonore elements (Mn, As, Ag, Sb, and Tl) associated with the Zn-Pb mineralizing hydrothermal fluids. Lithogeochemical data and statistical results corroborate the microanalytical findings. These elements are associated with both syngenetic to earliest diagenetic pyrite and later diagenetic pyrite overgrowths, suggesting that SEDEX mineralization was not only the product of hydrothermal precipitates that settled on the seafloor, but also dense metalliferous brine also settled on, and percolated through, unconsolidated carbonaceous muds and precipitated metals. This genetic model is similar to that proposed for the Paleoproterozoic HYC Zn-Pb-Ag SEDEX deposit in northern Australia, and it is likely that common processes and ambient conditions led to the formation and preservation of both of these large SEDEX districts.

  12. Age and tectonic setting of the Bavanat Cu-Zn-Ag Besshi-type volcanogenic massive sulfide deposit, southern Iran

    NASA Astrophysics Data System (ADS)

    Mousivand, Fardin; Rastad, Ebrahim; Meffre, Sebastien; Peter, Jan M.; Mohajjel, Mohammad; Zaw, Khin; Emami, Mohammad Hashem

    2012-12-01

    The Bavanat Cu-Zn-Ag Besshi-type volcanogenic massive sulfide (VMS) deposit occurs within the Surian volcano-sedimentary complex in the Sanandaj-Sirjan zone (SSZ) of southern Iran. The Surian complex is comprised of pelite, sandstone, calcareous shale, basalt, gabbro sills, and thin-bedded limestone. Mineralization occurs as stratiform sheet-like and tabular orebodies hosted mainly by greenschist metamorphosed feldspathic and quartz feldspathic sandstone, basalt, and pelites. The basalts of the Surian complex show predominantly tholeiitic to transitional affinities, with a few samples that are alkalic in composition. Primitive mantle-normalized trace and rare earth element (REE) patterns of the Surian basalts display depletions in light REE, negative anomalies of Nb, Ta, and Ti, and positive anomalies of P. Positive P anomalies are indicative of minor crustal contamination. Furthermore, Th enrichments in the mid-ocean ridge basalt-normalized patterns of the Surian basalts are characteristic of rifted arc basalts emplaced in continental margin subduction zones. The high MgO content (>6 wt.%) of most Surian basalts and low TiO2 content of two samples (0.53 and 0.62 wt.%) are characteristic of boninites. The aforementioned features of the basalts indicate arc tholeiites emplaced in intra-arc rift environments and continental margin subduction zones. U-Pb dating by laser ablation- inductively coupled plasma mass spectrometry of detrital zircons extracted from the host feldspathic and quartz feldspathic sandstone yields various ages that are predominantly Permian and Triassic; however, the youngest zircons give a mean Early Jurassic concordant U-Pb age of 191 ± 12 Ma. This age, together with geological and petrochemical data, indicate that VMS mineralization formed in the Early Jurassic in pull-apart basins within the SSZ. These basins and the VMS mineralization may be temporally related to an intra-arc volcano-plutonic event associated with Neo-Tethyan oblique

  13. Removal of Pb and Zn from contaminated soil by different washing methods: the influence of reagents and ultrasound.

    PubMed

    Wang, Jiaming; Jiang, Jianguo; Li, Dean; Li, Tianran; Li, Kaimin; Tian, Sicong

    2015-12-01

    Pb and Zn contamination in agricultural soils has become an important issue for human health and the environment. Washing is an effective method for remediating polluted soil. Here, we compare several washing materials and methods in the treatment of Pb- and Zn-polluted farmland soil. We examined four washing reagents, hydrochloric acid, citric acid, Na2EDTA, and tartaric acid, all of which independently removed Zn at rates >65 %. Combining washing reagents markedly enhanced heavy metal removal, by using Na2EDTA and either tartaric acid or lactate in sequence: Pb and Zn removal rates improved to 84.1 and 82.1 % for Na2EDTA-tartaric acid; and to 88.3 and 89.9 % for Na2EDTA-lactate, respectively. Additionally, combining ultrasound with conventional washing methods markedly improved washing efficiency, by shortening washing duration by 96 %. We achieved similar removal rates using ultrasound for 10 min, compared with traditional mechanical vibration alone for 4 h. We concluded that treating Pb- and Zn-contaminated soil with appropriate washing reagents under optimal conditions can greatly enhance the remediation of polluted farmland soils.

  14. Removal of Pb and Zn from contaminated soil by different washing methods: the influence of reagents and ultrasound.

    PubMed

    Wang, Jiaming; Jiang, Jianguo; Li, Dean; Li, Tianran; Li, Kaimin; Tian, Sicong

    2015-12-01

    Pb and Zn contamination in agricultural soils has become an important issue for human health and the environment. Washing is an effective method for remediating polluted soil. Here, we compare several washing materials and methods in the treatment of Pb- and Zn-polluted farmland soil. We examined four washing reagents, hydrochloric acid, citric acid, Na2EDTA, and tartaric acid, all of which independently removed Zn at rates >65 %. Combining washing reagents markedly enhanced heavy metal removal, by using Na2EDTA and either tartaric acid or lactate in sequence: Pb and Zn removal rates improved to 84.1 and 82.1 % for Na2EDTA-tartaric acid; and to 88.3 and 89.9 % for Na2EDTA-lactate, respectively. Additionally, combining ultrasound with conventional washing methods markedly improved washing efficiency, by shortening washing duration by 96 %. We achieved similar removal rates using ultrasound for 10 min, compared with traditional mechanical vibration alone for 4 h. We concluded that treating Pb- and Zn-contaminated soil with appropriate washing reagents under optimal conditions can greatly enhance the remediation of polluted farmland soils. PMID:26300361

  15. Chitosan film loaded with silver nanoparticles-sorbent for solid phase extraction of Al(III), Cd(II), Cu(II), Co(II), Fe(III), Ni(II), Pb(II) and Zn(II).

    PubMed

    Djerahov, Lubomir; Vasileva, Penka; Karadjova, Irina; Kurakalva, Rama Mohan; Aradhi, Keshav Krishna

    2016-08-20

    The present study describes the ecofriendly method for the preparation of chitosan film loaded with silver nanoparticles (CS-AgNPs) and application of this film as efficient sorbent for separation and enrichment of Al(III), Cd(II), Cu(II), Co(II), Fe(III), Ni(II), Pb(II) and Zn(II). The stable CS-AgNPs colloid was prepared by dispersing the AgNPs sol in chitosan solution at appropriate ratio and further used to obtain a cast film with very good stability under storage and good mechanical strength for easy handling in aqueous medium. The incorporation of AgNPs in the structure of CS film and interaction between the polymer matrix and nanoparticles were confirmed by UV-vis and FTIR spectroscopy. The homogeneously embedded AgNPs (average diameter 29nm, TEM analysis) were clearly observed throughout the film by SEM. The CS-AgNPs nanocomposite film shows high sorption activity toward trace metals under optimized chemical conditions. The results suggest that the CS-AgNPs nanocomposite film can be feasibly used as a novel sorbent material for solid-phase extraction of metal pollutants from surface waters.

  16. Influence of reactive sulfide (AVS) and supplementary food on Ag, Cd and Zn bioaccumulation in the marine polychaete Neanthes arenaceodentata

    USGS Publications Warehouse

    Lee, J.-S.; Lee, B.-G.; Yoo, H.; Koh, C.-H.; Luoma, S.N.

    2001-01-01

    A laboratory bioassay determined the relative contribution of various pathways of Ag, Cd and Zn bioaccumulation in the marine polychaete Neanthes arenaceodentata exposed to moderately contaminated sediments. Juvenile worms were exposed for 25 d to experimental sediments containing 5 different reactive sulfide (acid volatile sulfides, AVS) concentrations (1 to 30 ??mol g-1), but with constant Ag, Cd, and Zn concentrations of 0.1, 0.1 and 7 ??mol g-1, respectively. The sediments were supplemented with contaminated food (TetraMin??) containing 3 levels of Ag-Cd-Zn (uncontaminated, 1?? or 5??1 metal concentrations in the contaminated sediment). The results suggest that bioaccumulation of Ag, Cd and Zn in the worms occurred predominantly from ingestion of contaminated sediments and contaminated supplementary food. AVS or dissolved metals (in porewater and overlying water) had a minor effect on bioaccumulation of the 3 metals in most of the treatments. The contribution to uptake from the dissolved source was most important in the most oxic sediments, with maximum contributions of 8% for Ag, 30% for Cd and 20% for Zn bioaccumulation. Sediment bioassays where uncontaminated supplemental food is added could seriously underestimate metal exposures in an equilibrated system; N. arenaceodentata feeding on uncontaminated food would be exposed to 40-60% less metal than if the food source was equilibrated (as occurs in nature). Overall, the results show that pathways of metal exposure are dynamically linked in contaminated sediments and shift as external geochemical characteristics and internal biological attributes vary.

  17. Piezoelectric Properties of Fine-Grained Pb(Mg1/3Nb2/3)O3-Pb(Zr,Ti)O3-Bi(Zn1/2Ti1/2)O3 Quaternary Solid Solution Ceramics

    NASA Astrophysics Data System (ADS)

    Yue, Ruifang; Hou, Xianbo; He, Wenze; Yu, Jian

    2013-06-01

    On the basis of solid state reaction eutectic behavior between Pb(Mg1/3Nb2/3)O3-Pb(Zr,Ti)O3 (PMN-PZT) and metastable perovskite-type Bi(Zn1/2Ti1/2)O3 (BZT), perovskite-structured PMN-PZT-BZT quaternary solid solution piezoceramics with various compositions were experimentally demonstrated with an intrinsic low sintering temperature in the windows of 950-1050 °C. These fine-grained densified PMN-PZT-BZT ceramics were able to be poled sufficiently at room temperature through polarization-electric field hysteresis loop measurement, different from normal poling treatment with DC bias field at high temperature, which will simplify future device processing of monolithic multilayer piezoceramic transducers. A typical piezoelectric property of dielectric constant ɛ33T/ɛ0 = 3471, piezoelectric constant d33 = 480 pC/N, planar coupling coefficient kp = 0.41, thickness coupling coefficient kt = 0.50, mechanical quality factor Qm = 68 and relaxor ferroelectric phase transition temperature Tm = 167 °C at 1 MHz was obtained for the fine-grained densified Pb0.96Sr0.04(Mg1/3Nb2/3)0.37Zr0.24Ti0.39O3+3%Bi(Zn0.5Ti0.5)O3+2%NiO ceramics sintered at 1020 °C, which is much promising to manufacture monolithic multilayer piezoelectric transducers with Ag95/Pd5 as inner electrode material.

  18. Ultrasensitive SERS detection of trinitrotoluene through capillarity-constructed reversible hot spots based on ZnO-Ag nanorod hybrids.

    PubMed

    He, Xuan; Wang, Hui; Li, Zhongbo; Chen, Dong; Liu, Jiahui; Zhang, Qi

    2015-05-14

    A simple and efficient self-approach strategy was used to apply ultrasensitivity and self-revive ZnO-Ag hybrid surface-enhanced Raman scattering (SERS) sensors for the highly sensitive and selective detection of explosive TNT in both solution and vapour conditions. The good ultrasensitive sensing performance is a result of the abundant Raman hot spots, which were spontaneously formed in a reversible way by the self-approaching of flexible ZnO-Ag hybrid nanorods driven by the capillary force of solvent evaporation. Moreover, the enhancement effect was repeatedly renewed by the reconstruction of molecular bridges, which could selectively detect TNT with a lower limit of 4 × 10(-14) M. In addition, TNT vapor was also tested under this sensor, whereby once the ZnO-Ag NRs hybrid substrate was dipped in TNT, this substrate could detect the existence of TNT even in 5 detection cycles via a capillarity-constructed reversible hot spots approach. Compared with other pure Ag-based SERS sensors, this ZnO-Ag hybrid SERS sensor could rapidly self-revive SERS-activity by simple UV light irradiation and could retain stable SERS sensitivity for one month when used for TNT detection. This stable and ultrasensitive SERS substrate demonstrates a new route to eliminate the oxidized inactive problem of traditional Ag-based SERS substrates and suggests promising use in the applications of such hybrids as real-time online sensors for explosives detection.

  19. Mineral transformations and Zn, Pb, As, Cd mobility in soils developed on Zn non-sulfide mining wastes near Olkusz, S Poland

    NASA Astrophysics Data System (ADS)

    Jerzykowska, Irena; Michalik, Marek

    2014-05-01

    To estimate the degree of threat posed by heavy metals and other environmentally harmful elements it is necessary to determine forms in which these elements occur and their stability in the weathering environment. The aim of this work was to (1) describe mineral transformations occurring in soils developed on Zn non-sulfide mining wastes near Olkusz (S Poland), (2) identify forms of occurrence of Zn, Pb, As, Cd; and (3) predict potential mobility of these elements. Studied samples come from soil profiles developed on four dumps after mining of non-sulfide Zn ores from the end of the XIX century until 1985. Two types of approaches were used: mineralogical methods (optical and electron microscopy with in situ elemental analysis, X-ray diffraction) and geochemical methods (selective sequential extraction and bulk elemental analysis). Zn in studied samples is present in smithsonite or hemimorphite, Zn aluminosilicates (smectite and kaolinite groups) and absorbed on Fe-oxide. The largest amounts of Pb is encountered in Mn-oxides and less in cerrusite, Fe-oxides and dolomite. As dominates as the ions absorbed on goethite and Cd as an impurity in carbonates, silicates and Zn-aluminosilicates, and in the form of exchangeable ions. Most important mineral transformations due to weathering observed in the samples are dissolution of dolomite, goethite, smithsonite, hemimorphite and precipitation of Zn-aluminosilicates, Mn-oxides and secondary Fe-oxides. The study has shown that Cd occurring in the form of exchangeable ions, potentially available to living organisms, pose the greatest threat to the environment. Cd is the most mobile in surface horizons of the soils developed on the oxidized ores dumps. Zn and Pb can be released from their forms in the event of a change of pH of the environment to a more acidic and As in case of changing conditions to more reductive.

  20. Temperature-dependent photoluminescence properties of quaternary ZnAgInS quantum dots.

    PubMed

    Zhou, Ping; Zhang, Xiaosong; Liu, Xiaojuan; Xu, Jianping; Li, Lan

    2016-08-22

    A series of ZnAgInS (ZAIS) quantum dots were synthesized and their optical properties were tuned by adjusting the reaction times from 5 to 30 min. The emission spectra were observed ranging from 619 to 667 nm. The temperature-dependent photoluminescence properties of ZAIS QDs were investigated from 10 K to 300 K that show a blue shift of spectra line with increasing intensity as well as broadening of spectral line owing to the coupling of the carrier to acoustic phonon. We have also discussed and investigated the internal luminescence mechanism of ZAIS QDs. PMID:27557228

  1. Atmospheric-Pressure Processed Silver Nanowire (Ag-NW)/ZnO Composite Transparent Conducting Contacts

    SciTech Connect

    Perkins, John D.; Aggarwal, Shruti; van Hest, Maikel F. A. M.; Ginley, David S.

    2015-06-14

    Composite transparent contacts (TCs) based on metal nanowires and metal oxide matrix materials hold great promise for high performance transparent contacts for photovoltaics and opto-electronic technologies with the potential of all-atmospheric pressure processing. The metal nanowire mesh can provide both electrical conductivity and mechanical robustness against bending while the matrix material can both control the electrical interface and protect the metal nanowires. Here, we demonstrate all atmospheric pressure processed Ag-NW/ZnO composite TCs that are 90% transparent in the visible with sheet resistance Rs ~= 10 Ohms/sq. In addition, the composite TCs have higher infrared transmission than conventional TCO films with the same sheet resistance.

  2. Pb, Cu, and Zn distributions at humic acid-coated metal-oxide surfaces

    NASA Astrophysics Data System (ADS)

    Wang, Yingge; Michel, F. Marc; Choi, Yongseong; Eng, Peter J.; Levard, Clement; Siebner, Hagar; Gu, Baohua; Bargar, John R.; Brown, Gordon E.

    2016-09-01

    Mineral surfaces are often coated by natural organic matter (NOM), which has a major influence on metal-ion sorption and sequestration because of the abundance of binding sites in such coatings and the changes they cause in local nanoscale environments. The effects of NOM coatings on mineral surfaces are, however, still poorly understood at the molecular level due to the complexity of these systems. In this study, we have applied long-period X-ray standing wave-fluorescence yield (LP-XSW-FY) spectroscopy to measure the partitioning of naturally present Cu(II) (0.0226%), Zn(II) (0.009%), and Pb(II) (∼0.0004%) between Elliott Soil Humic Acid (ESHA) coatings and three model single-crystal metal-oxide substrates: α-Al2O3 (0 0 0 1), α-Al2O3 (1 -1 0 2), and α-Fe2O3 (0 0 0 1). The competitive sorption effects among these metal ions for binding sites in the ESHA coatings and on the metal-oxide surfaces were investigated as a function of reaction time, calcium content, and solution pH. Pb(II) ions present in the ESHA coatings were found to redistribute to reactive α-Al2O3 (1 -1 0 2) and α-Fe2O3 (0 0 0 1) surfaces after 3 h of reaction (pH = 6.0, [Ca(II)] = 2 mM). Pb(II) partitioning onto these reactive metal-oxide surfaces increased with increasing reaction time (up to 7 d). In addition, the partitioning of Cu(II) and Zn(II) from the ESHA coating to the α-Fe2O3 (0 0 0 1) substrate increased slightly with reaction time (2.4% and 3.7% for Cu(II) and Zn(II), respectively, after 3 h and 6.4% and 7.7% for Cu(II) and Zn(II), respectively, after 72 h of reaction time). However, no changes in the partitioning of Cu(II) and Zn(II) onto the α-Al2O3 (1 -1 0 2) surface were observed with increasing reaction time, suggesting that these ions strongly complex with functional groups in the ESHA coatings. Similar results were obtained for Cu(II) and Zn(II) on the ESHA-coated α-Al2O3 (1 -1 0 2) surfaces in samples without the addition of calcium. However, the amounts of Pb

  3. Did a whole-crustal hydrothermal system generate the Irish Zn-Pb orefield?

    NASA Astrophysics Data System (ADS)

    Daly, J. Stephen; Badenszki, Eszter; Chew, David; Kronz, Andreas; O'Rourke, Helen; Whitehouse, Martin; Menuge, Julian; van den Berg, Riana

    2016-04-01

    Current models[1] for the genesis of the giant Irish Carboniferous-hosted Zn-Pb orefield propose shallow (<10 km depth) hydrothermal circulation within Lower Palaeozoic basement rocks of the Iapetus Suture Zone as the main metal source. However several lines of evidence, e.g., from He[2], S[2,3] and Os[4] isotopes, and the possible role of contemporary volcanism[5] point to deeper, including mantle, fluid source(s) and/or pathways. The Iapetus Suture Zone in Ireland is uniquely favoured to evaluate the scale of hydrothermal circulation because of the presence there of granulite-facies lower crustal xenoliths at four widely separated localities. These were carried to the surface from ~22-28km (and deeper levels) by Lower Carboniferous alkali basaltic lavas and diatremes[6,7]. They provide the only possible direct samples of the lower crust and are of appropriate age. U-Pb zircon geochronology demonstrates that the xenoliths experienced high temperature (>700°C) metamorphism and melting during the Acadian orogeny at ~390Ma and during separate episodes of extension at ~ 381-373Ma and ~362Ma. Sm-Nd garnet dating shows that the lower crust remained hot or was re-heated to ~600°C at ~341Ma during Lower Carboniferous volcanism, also associated with extension and, in part, coincident with the mineralization[1]. Isotopic data from the xenoliths correspond closely to Sr and Nd isotopic analyses of gangue calcite[8] and galena Pb[9] isotopic data from the major ore deposits. While Zn contents of the xenoliths permit them to be metal sources, their mineralogy and texture provide an enriched template and a plausible extraction mechanism. In situ analyses of modally-abundant biotite and garnet show significant enrichment in Zn (and other relevant metals) as well as order of magnitude depletion of Zn during retrograde alteration, providing a metal-release mechanism and pointing to a hydrothermal fluid system operating at least to depths of ~ 25km. References [1] Wilkinson, J

  4. Formation of recent Pb-Ag-Au mineralization by potential sub-surface microbial activity.

    PubMed

    Tornos, Fernando; Velasco, Francisco; Menor-Salván, César; Delgado, Antonio; Slack, John F; Escobar, Juan Manuel

    2014-08-06

    Las Cruces is a base-metal deposit in the Iberian Pyrite Belt, one of the world's best-known ore provinces. Here we report the occurrence of major Pb-Ag-Au mineralization resulting from recent sub-surface replacement of supergene oxyhydroxides by carbonate and sulphide minerals. This is probably the largest documented occurrence of recent microbial activity producing an ore assemblage previously unknown in supergene mineralizing environments. The presence of microbial features in the sulphides suggests that these may be the first-described natural bacteriomorphs of galena. The low δ(13)C values of the carbonate minerals indicate formation by deep anaerobic microbial processes. Sulphur isotope values of sulphides are interpreted here as reflecting microbial reduction in a system impoverished in sulphate. We suggest that biogenic activity has produced around 3.1 × 10(9) moles of reduced sulphur and 10(10) moles of CO2, promoting the formation of ca. 1.19 Mt of carbonates, 114,000 t of galena, 638 t of silver sulphides and 6.5 t of gold.

  5. Formation of recent Pb-Ag-Au mineralization by potential sub-surface microbial activity

    NASA Astrophysics Data System (ADS)

    Tornos, Fernando; Velasco, Francisco; Menor-Salván, César; Delgado, Antonio; Slack, John F.; Escobar, Juan Manuel

    2014-08-01

    Las Cruces is a base-metal deposit in the Iberian Pyrite Belt, one of the world’s best-known ore provinces. Here we report the occurrence of major Pb-Ag-Au mineralization resulting from recent sub-surface replacement of supergene oxyhydroxides by carbonate and sulphide minerals. This is probably the largest documented occurrence of recent microbial activity producing an ore assemblage previously unknown in supergene mineralizing environments. The presence of microbial features in the sulphides suggests that these may be the first-described natural bacteriomorphs of galena. The low δ13C values of the carbonate minerals indicate formation by deep anaerobic microbial processes. Sulphur isotope values of sulphides are interpreted here as reflecting microbial reduction in a system impoverished in sulphate. We suggest that biogenic activity has produced around 3.1 × 109 moles of reduced sulphur and 1010 moles of CO2, promoting the formation of ca. 1.19 Mt of carbonates, 114,000 t of galena, 638 t of silver sulphides and 6.5 t of gold.

  6. Thermoelectric Inhomogeneities in (Ag(sub 1-y)SbTe2)(sub x)(PbTe)(sub 1-x)

    NASA Technical Reports Server (NTRS)

    Snyder, G. Jeffrey; Chen, Nancy; Gascoin, Franck; Mueller, Eckhard; Karpinski, Gabriele; Stiewe, Christian

    2006-01-01

    A document presents a study of why materials of composition (Ag1 ySbTe2)0.05 (PbTe)0.95 [0< or = y < or = 1] were previously reported to have values of the thermoelectric figure of merit [ZT (where Z = alpha(sup 2)/rk, alpha is the Seebeck coefficient, r is electrical resistivity, k is thermal conductivity, and T is absolute temperature)] ranging from <1 to >2. In the study, samples of (AgSbTe2)0.05(PbTe)0.95, (Ag0.67SbTe2)0.05 (PbTe)0.95, and (Ag0.55SbTe2)0.05(PbTe)0.95 were prepared by melting followed, variously, by slow or rapid cooling. Analyses of these samples by x-ray diffraction, electron microscopy, and scanning-microprobe measurements of the Seebeck coefficient led to the conclusion that these materials have a multiphase character on a scale of the order of millimeters, even though they appear homogeneous in x-ray diffraction and electron microscopy. The Seebeck measurements showed significant variations, including both n-type and p-type behavior in the same sample. These variations were found to be consistent with observed variations of ZT. The rapidly quenched samples were found to be less inhomogeneous than were the furnace-cooled ones; hence, rapid quenching was suggested as a basis of research on synthesizing more nearly uniform high-ZT samples.

  7. Electrochemical route to the synthesis of ZnO microstructures: its nestlike structure and holding of Ag particles

    PubMed Central

    2013-01-01

    Abstract A simple and facile electrochemical route was developed for the shape-selective synthesis of large-scaled series of ZnO microstructures, including petal, flower, sphere, nest and clew aggregates of ZnO laminas at room temperature. This route is based on sodium citrate-directed crystallization. In the system, sodium citrate can greatly promote ZnO to nucleate and directly grow by selectively capping the specific ZnO facets because of its excellent adsorption ability. The morphology of ZnO is tuned by readily adjusting the concentration of sodium citrate and the electrodeposition time. Among the series structures, the remarkable ZnO nestlike structure can be used as a container to hold not only the interlaced ZnO laminas but also Ag nanoparticles in the center. The special heterostructures of nestlike ZnO holding Ag nanoparticles were found to display the superior properties on the surface-enhanced Raman scattering. This work has signified an important methodology to produce a wide assortment of desired microstructures of ZnO. PACS 81 Materials science 81.07.-b nanoscale materials and structures Fabrication Characterization 81.15.-z Methods of deposition of films Coatings Film growth and epitaxy. PMID:23414592

  8. Electrochemical route to the synthesis of ZnO microstructures: its nestlike structure and holding of Ag particles.

    PubMed

    Ding, Ling; Zhang, Ruixue; Fan, Louzhen

    2013-02-15

    A simple and facile electrochemical route was developed for the shape-selective synthesis of large-scaled series of ZnO microstructures, including petal, flower, sphere, nest and clew aggregates of ZnO laminas at room temperature. This route is based on sodium citrate-directed crystallization. In the system, sodium citrate can greatly promote ZnO to nucleate and directly grow by selectively capping the specific ZnO facets because of its excellent adsorption ability. The morphology of ZnO is tuned by readily adjusting the concentration of sodium citrate and the electrodeposition time. Among the series structures, the remarkable ZnO nestlike structure can be used as a container to hold not only the interlaced ZnO laminas but also Ag nanoparticles in the center. The special heterostructures of nestlike ZnO holding Ag nanoparticles were found to display the superior properties on the surface-enhanced Raman scattering. This work has signified an important methodology to produce a wide assortment of desired microstructures of ZnO. PACS: 81 Materials science 81.07.-b nanoscale materials and structures Fabrication Characterization 81.15.-z Methods of deposition of films Coatings Film growth and epitaxy.

  9. Hierarchical ZnO-Ag-C composite porous microspheres with superior electrochemical properties as anode materials for lithium ion batteries.

    PubMed

    Xie, Qingshui; Ma, Yating; Zeng, Deqian; Zhang, Xiaoqiang; Wang, Laisen; Yue, Guanghui; Peng, Dong-Liang

    2014-11-26

    Hierarchical ZnO-Ag-C composite porous microspheres are successfully synthesized by calcination of the preproduced zinc-silver citrate porous microspheres in argon. The carbon derives from the in situ carbonization of carboxylic acid groups in zinc-silver citrate during annealing treatment. The average particle size of ZnO-Ag-C composite porous microspheres is approximate 1.5 μm. When adopted as the electrode materials in lithium ion batteries, the obtained composite porous microspheres display high specific capacity, excellent cyclability, and good rate capability. A discharge capacity as high as 729 mA h g(-1) can be retained after 200 cycles at 100 mA g(-1). The excellent electrochemical properties of ZnO-Ag-C are ascribed to its unique hierarchical porous configuration as well as the modification of silver and carbon.

  10. Hexagonal core-shell and alloy Au/Ag nanodisks on ZnO nanorods and their optical enhancement effect

    PubMed Central

    2014-01-01

    Au and Ag hybrid hexagonal nanodisks were synthesized on ZnO nanorods' (0002) surface via a new two-step deposition-annealing method. The structural, compositional, as well as optical investigations were carried out systematically to find out the nanodisks' formation mechanism and optical enhancement effect. It was shown that the core-shell Au/Ag nanodisk can be formed under rapid annealing temperature of 500°C, while Au/Ag alloy nanodisks are formed if higher temperatures (>550°C) are applied. The optical effect from these nanodisks was studied through photoluminescence and absorption spectroscopy. It was found that the carrier-plasmon coupling together and carrier transfer between metal and ZnO contribute to the emission enhancement. Furthermore, the results suggest that the composition of nanodisk on the vicinity of metal/ZnO interface plays an important role in terms of the enhancement factors. PMID:24936157

  11. Spatial and temporal variations in inhalable CuZnPb aerosols within the Mexico City pollution plume.

    PubMed

    Moreno, T; Querol, X; Pey, J; Minguillón, M C; Pérez, N; Alastuey, A; Bernabé, R M; Blanco, S; Cárdenas, B; Eichinger, W; Salcido, A; Gibbons, W

    2008-03-01

    We report on the CuPbZn content of PM10 and PM2.5 samples collected from three sites (urban T0, suburban T1 and rural T2) during the Mexico City MILAGRO campaign of March 2006. Daytime city centre concentrations of summation operator CuZnPb(PM10) were much higher (T0 > 450 ng m(-3)) than at the suburban site (T1 < 200 ng m(-3)). Rural site (T2) summation operator CuZnPb(PM10) concentrations exceeded 50 ng m(-3) when influenced by the megacity plume but dropped to 10 ng m(-3) during clean northerly winds. Nocturnal metal concentrations more than doubled at T0, as pollutants became trapped in the nightly inversion layer, but decreased at the rural site. Transient spikes in concentrations of different metals, e.g. a "copper event" at T0 (CuPM10 281 ng m(-3)) and "zinc event" at T1 (ZnPM10 1481 ng m(-3)) on the night of March 7-8, demonstrate how industrial pollution sources produce localised chemical inhomogeneities in the city atmosphere. Most metal aerosols are <2.5 microm and SEM study demonstrates the dominance of Fe, Ti, Ba, Cu, Pb and Zn (and lesser Sn, Mo, Sb, W, Ni, V, As, Bi) in metalliferous particles that have shapes including spherical condensates, efflorescent CuZnClS particles, cindery Zn, and Cu wire. Metal aerosol concentrations do not change in concert with PM10 mass, which is more influenced by wind resuspension than industrial emissions. Metalliferous particles can induce cell damage, and PM composition is probably more important than PM mass, with respect to negative health effects, so that better monitoring and control of industrial emissions would likely produce significant improvements in air quality.

  12. Pb-Bi-Ag-Cu-(Hg) chemistry of galena and some associated sulfosalts. A review and some new data from Colorado California and Pennsylvania

    USGS Publications Warehouse

    Foord, Eugene E.; Shawe, Daniel R.

    1989-01-01

    Galena, associated with Pb-Bi-Ag sulfosalts and simple sulfides, contains varied amounts of Ag and Bi in the Dandy vein system, Idarado mine, Ouray, Colorado; the Jackass mine, Darwin District, California; and the Leadville district, Colorado. Silver- and bismuth-bearing galena associated with minor amounts of pyrite, chalcopyrite and sphalerite occur at the Pequea mine, Lancaster County, Pennsylvania. Ag and Bi contents in the Dandy suite of galena range from about 1.4 to 3.4 and 2.5 to 6.5 wt.% respectively, and are comparable or lower in galena from the other localities. Exsolved matildite is present in galena from the Dandy, Jackass and Leadville localities. The presence in significant amounts of both Ag and Bi in a Pb-rich sulfide system is necessary for formation of PbSss (galena solid-solution). If Ag (especially) and Bi (to a lesser extent) are absent, the galena formed will be essentially pure PbS. Some minor Sb may substitute for Bi. Compositional data for all of the galena samples are in agreement with a previously proposed linear relationship between a and Ag-Bi(Sb) content. Matildite and seven additional Pb-Bi-Ag-Cu sulfosalts have been identified from the Dandy vein system, based on electron-microprobe analyses and some X-ray powder-diffraction data.

  13. Synthesis, characterization and application of ZnO-Ag as a nanophotocatalyst for organic compounds degradation, mechanism and economic study.

    PubMed

    Mohammadzadeh, S; Olya, M E; Arabi, A M; Shariati, A; Khosravi Nikou, M R

    2015-09-01

    The current work deals with ZnO-Ag nanocomposites (in the wide range of x in the Zn1-xO-Agx chemical composition) synthesized using microwave assisted solution combustion method. The structural, morphological and optical properties of the samples were characterized by XRD (X-ray diffraction), FTIR (Fourier transform infrared spectrometry), SEM (scanning electron microscopy technique), EDX (energy dispersive X-ray spectrum), ICP (inductively coupled plasma technique), TEM (transmission electron microscopy), BET (Brunauer-Emmett-Teller method), UV-Vis (ultraviolet-visible spectrophotometer) and photoluminescence spectrophotometer. The photocatalytic activity of the ZnO-Ag was investigated by photo-degradation of Acid Blue 113 (AB 113) under UV illumination in a semi-batch reactor. This experiment showed that ZnO-Ag has much more excellent photocatalytic properties than ZnO synthesized by the same method. The enhanced photocatalytic activity was due to the decrease in recombination of photogenerated electron-holes. The results showed the improvement of ZnO photocatalytic activity and there is an optimum amount of Ag (3.5mol%) that needs to be doped with ZnO. The effect of operating parameters such as pH, catalyst dose and dye concentration were investigated. The reaction byproducts were identified by LC/MS (liquid chromatography/mass spectrometry) analysis and a pathway was proposed as well. Kinetic studies indicated that the decolorization process follows the first order kinetics. Also, the degradation percentage of AB 113 was determined using a total organic carbon (TOC) analyzer. Additionally, cost analysis of the process, the mechanism and the role of Ag were discussed. PMID:26354709

  14. Synthesis, characterization and application of ZnO-Ag as a nanophotocatalyst for organic compounds degradation, mechanism and economic study.

    PubMed

    Mohammadzadeh, S; Olya, M E; Arabi, A M; Shariati, A; Khosravi Nikou, M R

    2015-09-01

    The current work deals with ZnO-Ag nanocomposites (in the wide range of x in the Zn1-xO-Agx chemical composition) synthesized using microwave assisted solution combustion method. The structural, morphological and optical properties of the samples were characterized by XRD (X-ray diffraction), FTIR (Fourier transform infrared spectrometry), SEM (scanning electron microscopy technique), EDX (energy dispersive X-ray spectrum), ICP (inductively coupled plasma technique), TEM (transmission electron microscopy), BET (Brunauer-Emmett-Teller method), UV-Vis (ultraviolet-visible spectrophotometer) and photoluminescence spectrophotometer. The photocatalytic activity of the ZnO-Ag was investigated by photo-degradation of Acid Blue 113 (AB 113) under UV illumination in a semi-batch reactor. This experiment showed that ZnO-Ag has much more excellent photocatalytic properties than ZnO synthesized by the same method. The enhanced photocatalytic activity was due to the decrease in recombination of photogenerated electron-holes. The results showed the improvement of ZnO photocatalytic activity and there is an optimum amount of Ag (3.5mol%) that needs to be doped with ZnO. The effect of operating parameters such as pH, catalyst dose and dye concentration were investigated. The reaction byproducts were identified by LC/MS (liquid chromatography/mass spectrometry) analysis and a pathway was proposed as well. Kinetic studies indicated that the decolorization process follows the first order kinetics. Also, the degradation percentage of AB 113 was determined using a total organic carbon (TOC) analyzer. Additionally, cost analysis of the process, the mechanism and the role of Ag were discussed.

  15. Immobilisation of Cu, Pb and Zn in Scrap Metal Yard Soil Using Selected Waste Materials.

    PubMed

    Kamari, A; Putra, W P; Yusoff, S N M; Ishak, C F; Hashim, N; Mohamed, A; Isa, I M; Bakar, S A

    2015-12-01

    Immobilisation of heavy metals in a 30-year old active scrap metal yard soil using three waste materials, namely coconut tree sawdust (CTS), sugarcane bagasse (SB) and eggshell (ES) was investigated. The contaminated soil was amended with amendments at application rates of 0 %, 1 % and 3 % (w/w). The effects of amendments on metal accumulation in water spinach (Ipomoea aquatica) and soil metal bioavailability were studied in a pot experiment. All amendments increased biomass yield and reduced metal accumulation in the plant shoots. The bioconcentration factor and translocation factor values of the metals were in the order of Zn > Cu > Pb. The addition of ES, an alternative source of calcium carbonate (CaCO3), has significantly increased soil pH and resulted in marked reduction in soil metal bioavailability. Therefore, CTS, SB and ES are promising low-cost immobilising agents to restore metal contaminated land. PMID:26395356

  16. Immobilisation of Cu, Pb and Zn in Scrap Metal Yard Soil Using Selected Waste Materials.

    PubMed

    Kamari, A; Putra, W P; Yusoff, S N M; Ishak, C F; Hashim, N; Mohamed, A; Isa, I M; Bakar, S A

    2015-12-01

    Immobilisation of heavy metals in a 30-year old active scrap metal yard soil using three waste materials, namely coconut tree sawdust (CTS), sugarcane bagasse (SB) and eggshell (ES) was investigated. The contaminated soil was amended with amendments at application rates of 0 %, 1 % and 3 % (w/w). The effects of amendments on metal accumulation in water spinach (Ipomoea aquatica) and soil metal bioavailability were studied in a pot experiment. All amendments increased biomass yield and reduced metal accumulation in the plant shoots. The bioconcentration factor and translocation factor values of the metals were in the order of Zn > Cu > Pb. The addition of ES, an alternative source of calcium carbonate (CaCO3), has significantly increased soil pH and resulted in marked reduction in soil metal bioavailability. Therefore, CTS, SB and ES are promising low-cost immobilising agents to restore metal contaminated land.

  17. Trace level determination of u, zn, cd, pb and cu in drinking water samples.

    PubMed

    Kumar, Mukesh; Singh, Surinder; Mahajan, Rakesh Kumar

    2006-01-01

    The concentration of uranium has been assessed in drinking water samples collected from different locations in Bathinda district, Punjab, India. The water samples are taken from hand pumps and tube wells. Uranium is determined using fission track technique. Uranium concentration in the water samples varies from 2.23+/- 0.05 to 87.05+/- 0.29 microg/L. These values are compared with safe limit values recommended for drinking water. The uranium concentration in almost all drinking water samples is found to be more than the safe limit. Analysis of some heavy metals viz. Zn, Cd, Pb and Cu in water is made. The concentration of sodium, potassium, calcium, magnesium, chlorine and total hardness along with the pH value and conductivity of the water samples are measured. Some of the samples show stunningly high values of these parameters.

  18. Tuning of Ag doped core-shell ZnO NWs/Cu2O grown by electrochemical deposition

    NASA Astrophysics Data System (ADS)

    Makhlouf, Houssin; Messaoudi, Olfa; Souissi, Ahmed; Ben Assaker, Ibtissem; Oueslati, Mihrez; Bechelany, Mikhael; Chtourou, Radhouane

    2015-09-01

    ZnO nanowires (NWs)/Cu2O-Ag core-shell nanostructures (NSs) have been synthesized by electrochemical deposition method on ITO-coated glass substrates in order to improve the efficiency of the type-II transition of core-shell ZnO NWs/Cu2O-Ag NSs. The morphologies of the obtained NSs were studied by scanning electron microscopy confirming the presence of core-shell NSs. The crystalline proprieties were analyzed by x-ray diffraction and micro-Raman measurement: wurtzite ZnO and cuprit Cu2O phase were founded. The presence of Ag content in core-shell NS was detected by EDX. Optical measurement reveals an additional contribution δE at about 1.72 eV attributed to the type-II interfacial transition between the valance band of cuprit-Cu2O and the conduction band of W-ZnO. The effect of the Ag doping into the type-II transition was investigated. A red shift of the type-II transition was detected according to the Ag concentration. These materials could have potential applications in photocatalytic and photovoltaic fields.

  19. Tetrahedron dynamics in the icosahedral quasicrystals i-ZnMgSc and i-ZnAgSc and the cubic 1/1-approximant Zn6Sc.

    PubMed

    Euchner, H; Yamada, T; Rols, S; Ishimasa, T; Kaneko, Y; Ollivier, J; Schober, H; Mihalkovic, M; de Boissieu, M

    2013-03-20

    A comparison of periodic approximants and their quasicrystalline counterparts offers the opportunity to better understand the structure, physical properties and stabilizing mechanisms of these complex phases. We present a combined experimental and molecular dynamics study of the lattice dynamics of the icosahedral quasicrystals i-ZnMgSc and i-ZnAgSc and compare it to recently published results obtained for the cubic 1/1-approximant Zn(6)Sc. Both phases, quasicrystal and approximant, are built up from large atomic clusters which contain a tetrahedral shell at the cluster centre and are packed either quasiperiodically or on a bcc lattice. Using quasielastic neutron scattering and atomic scale simulations, we show that in the quasicrystal the tetrahedra display a dynamics similar to that observed in the 1/1-approximant: the tetrahedra behave as a 'single molecule' and reorient dynamically on a timescale of the order of a few ps. The tetrahedra reorientation is accompanied by a large distortion of the surrounding cluster shells which provide a unique dynamical flexibility to the quasicrystal. However, whereas in the 1/1-approximant the tetrahedron reorientation is observed down to T(c) = 160 K, where a phase transition takes place, in the quasicrystal the tetrahedron dynamics is gradually freezing from 550 to 300 K, similarly to a glassy system.

  20. Ag2ZnSn(S,Se)4: A highly promising absorber for thin film photovoltaics.

    PubMed

    Chagarov, Evgueni; Sardashti, Kasra; Kummel, Andrew C; Lee, Yun Seog; Haight, Richard; Gershon, Talia S

    2016-03-14

    The growth in efficiency of earth-abundant kesterite Cu2ZnSn(S,Se)4 (CZTSSe) solar cells has slowed, due in part to the intrinsic limitations imposed by the band tailing attributed primarily to I-II antisite exchange. In this study, density functional theory simulations show that when Ag is substituted for Cu to form kesterite Ag2ZnSnSe4 (AZTSe), the I-II isolated antisite formation energy becomes 3.7 times greater than in CZTSSe, resulting in at least an order of magnitude reduction in I-II antisite density. Experimental evidence of an optoelectronically improved material is also provided. Comparison of the low-temperature photoluminescence (PL) structure of Cu(In,Ga)Se2 (CIGSe), CZTSSe, and AZTSe shows that AZTSe has a shallow defect structure with emission significantly closer to the band edge than CZTSe. Existence of suppressed band tailing is found in the proximity of the room-temperature PL peak of AZTSe to its measured band gap. The results are consistent with AZTSe being a promising alternative to CZTSSe and CIGSe for thin film photovoltaics.

  1. Ag2ZnSn(S,Se)4: A highly promising absorber for thin film photovoltaics.

    PubMed

    Chagarov, Evgueni; Sardashti, Kasra; Kummel, Andrew C; Lee, Yun Seog; Haight, Richard; Gershon, Talia S

    2016-03-14

    The growth in efficiency of earth-abundant kesterite Cu2ZnSn(S,Se)4 (CZTSSe) solar cells has slowed, due in part to the intrinsic limitations imposed by the band tailing attributed primarily to I-II antisite exchange. In this study, density functional theory simulations show that when Ag is substituted for Cu to form kesterite Ag2ZnSnSe4 (AZTSe), the I-II isolated antisite formation energy becomes 3.7 times greater than in CZTSSe, resulting in at least an order of magnitude reduction in I-II antisite density. Experimental evidence of an optoelectronically improved material is also provided. Comparison of the low-temperature photoluminescence (PL) structure of Cu(In,Ga)Se2 (CIGSe), CZTSSe, and AZTSe shows that AZTSe has a shallow defect structure with emission significantly closer to the band edge than CZTSe. Existence of suppressed band tailing is found in the proximity of the room-temperature PL peak of AZTSe to its measured band gap. The results are consistent with AZTSe being a promising alternative to CZTSSe and CIGSe for thin film photovoltaics. PMID:26979701

  2. Ag2ZnSn(S,Se)4: A highly promising absorber for thin film photovoltaics

    NASA Astrophysics Data System (ADS)

    Chagarov, Evgueni; Sardashti, Kasra; Kummel, Andrew C.; Lee, Yun Seog; Haight, Richard; Gershon, Talia S.

    2016-03-01

    The growth in efficiency of earth-abundant kesterite Cu2ZnSn(S,Se)4 (CZTSSe) solar cells has slowed, due in part to the intrinsic limitations imposed by the band tailing attributed primarily to I-II antisite exchange. In this study, density functional theory simulations show that when Ag is substituted for Cu to form kesterite Ag2ZnSnSe4 (AZTSe), the I-II isolated antisite formation energy becomes 3.7 times greater than in CZTSSe, resulting in at least an order of magnitude reduction in I-II antisite density. Experimental evidence of an optoelectronically improved material is also provided. Comparison of the low-temperature photoluminescence (PL) structure of Cu(In,Ga)Se2 (CIGSe), CZTSSe, and AZTSe shows that AZTSe has a shallow defect structure with emission significantly closer to the band edge than CZTSe. Existence of suppressed band tailing is found in the proximity of the room-temperature PL peak of AZTSe to its measured band gap. The results are consistent with AZTSe being a promising alternative to CZTSSe and CIGSe for thin film photovoltaics.

  3. Electrochemical depositions of fluorohydroxyapatite doped by Cu2+, Zn2+, Ag+ on stainless steel substrates

    NASA Astrophysics Data System (ADS)

    Bir, F.; Khireddine, H.; Touati, A.; Sidane, D.; Yala, S.; Oudadesse, H.

    2012-07-01

    Fluoridated hydroxyapatite (FHA, Ca10(PO4)6(OH)2-xFx where 0 < x < 2 is the degree of fluoridation) and inorganic ions (Zn2+, Cu2+, Ag+) substituted fluoridated hydroxyapatite coatings (M-FHA) were deposited on the surface of medical grade 316L stainless steel samples by electrochemical deposition technique. The FHA coatings were co-substituted with antibacterial ions (Zn2+, Cu2+ or Ag+) by co-precipitation and ion-exchange methods. Characterization studies of coatings from X-ray diffraction (XRD), Scanning electron microscopy (SEM) and Energy dispersive X-ray spectroscopy (EDX) showed that the obtained layers are monophase crystals FHA and did not contain any discernible crystalline impurity. The particles of all samples are of nano size that gives thin layers. The surface morphology, microstructure and Ca/P atomic ratio of the FHA coatings can be regulated by varying electrolyte temperature. This later affects the porosity of the coating surface and the chemical compositions of the deposits. Quantitative elemental analysis indicates that the copper, zinc and silver ions are incorporated into the Fluorohydroxyapatite. The antimicrobial effects of doped fluorohydroxyapatite coatings against pathogen bacterial strains Staphylococcus aureus were tested in liquid media. The results are promising and demonstrated that all doped FHA samples exhibit excellent antimicrobial activity "in vitro" against the microorganism, so the antimicrobial properties of the coatings developed are improved.

  4. ZnO-Ag hybrids for ultrasensitive detection of trinitrotoluene by surface-enhanced Raman spectroscopy.

    PubMed

    He, Xuan; Wang, Hui; Li, Zhongbo; Chen, Dong; Zhang, Qi

    2014-07-28

    An efficient and green approach was used to fabricate novel and low-cost surface-enhanced Raman scattering (SERS) spectroscopy sensors based on 4-aminothiophenol (4-ATP) functionalized ZnO-Ag hybrid nanoflowers for the detection of explosives. Such SERS sensors exhibited high sensitivity to rhodamine 6G (R6G) at a low concentration of 10(-12) M and an enhancement factor of over 4.12 × 10(6) was achieved. Moreover, the Raman-inactive trinitrotoluene (TNT) initiated the high Raman scattering of non-resonated 4-ATP through the formation of a π-donor-π-acceptor interaction between the π-acceptor, TNT, and the π-donor, the 4-ATP-Ag-ZnO complex, on the flower-like hybrids. Because this π-donor-π-acceptor interaction could effectively induce the "hot spots" for SERS, TNT concentrations as low as 5 × 10(-9) M could be detected. Furthermore, other derivatives of TNT were also explored, and this sensor exhibited better selectivity for TNT than other similarly structured explosives. The low-cost hybrid SERS substrates presented good sensitivity and reproducibility for the analytes employed, demonstrating promising application in forensic science and homeland security.

  5. Variability in the fractionation of Cu, Ag, and Zn among cytosolic proteins in the bivalve Macoma balthica

    USGS Publications Warehouse

    Johansson, C.; Cain, Daniel J.; Luoma, Samuel N.

    1986-01-01

    Gel filtration chromatographs of cytosols from the clam Macorna balthica analysed from both field and laboratory treated specimens showed that uptake of Cu, Ag, and Zn in the metallothionein-like protein (MLP) pool follows exposure both in nature and in the laboratory. Specimens collected from San Francisco Bay over 18 mo showed strong temporal variability in the fractionation of the metals among cytosolic proteins. A marked increase in Cu, Ag, and Zn in a very low molecular weight pool occurred when concentrations were highest In the MLP pool. The correlation between total cytosollc metal and MLP-metal also appeared to approach a hyperbolic character at the highest concentrations.

  6. A theoretical study of a ZnO graphene analogue: adsorption on Ag(111) and hydrogen transport.

    PubMed

    Demiroglu, Ilker; Stradi, Daniele; Illas, Francesc; Bromley, Stefan T

    2011-08-24

    A single sheet of zinc oxide (ZnO) based on the same flat two-dimensional (2D) hexagonal topology as graphene, but with alternating neighbouring Zn and O atoms in place of carbon atoms, is studied theoretically. Following experimental studies, the adsorption of 2D-ZnO with the Ag(111) surface is investigated using density functional theory, with and without a semi-empirical correction for dispersive interactions, and with classical interatomic potentials. The interaction of H atoms with the hexagonal Zn(3)O(3) rings of 2D-ZnO is given special attention where multi-centre bond formation is observed to significantly assist the transport of H atoms through the 2D-ZnO sheet.

  7. Quantum dot size dependent J-V characteristics in heterojunction ZnO/PbS quantum dot solar cells.

    PubMed

    Gao, Jianbo; Luther, Joseph M; Semonin, Octavi E; Ellingson, Randy J; Nozik, Arthur J; Beard, Matthew C

    2011-03-01

    The current-voltage (J-V) characteristics of ZnO/PbS quantum dot (QD) solar cells show a QD size-dependent behavior resulting from a Schottky junction that forms at the back metal electrode opposing the desirable diode formed between the ZnO and PbS QD layers. We study a QD size-dependent roll-over effect that refers to the saturation of photocurrent in forward bias and crossover effect which occurs when the light and dark J-V curves intersect. We model the J-V characteristics with a main diode formed between the n-type ZnO nanocrystal (NC) layer and p-type PbS QD layer in series with a leaky Schottky-diode formed between PbS QD layer and metal contact. We show how the characteristics of the two diodes depend on QD size, metal work function, and PbS QD layer thickness, and we discuss how the presence of the back diode complicates finding an optimal layer thickness. Finally, we present Kelvin probe measurements to determine the Fermi level of the QD layers and discuss band alignment, Fermi-level pinning, and the V(oc) within these devices.

  8. Near-infrared emitting AgInTe2 and Zn-Ag-In-Te colloidal nanocrystals

    NASA Astrophysics Data System (ADS)

    Langevin, Marc-Antoine; Pons, Thomas; Ritcey, Anna M.; Nì. Allen, Claudine

    2015-06-01

    The synthesis of AgInTe2 nanocrystals emitting between 1095 nm and 1160 nm is presented. Evolution of the Ag:In:Te ratio shows progressive incorporation of In3+ in Ag2Te, leading to the formation of orthorhombic AgInTe2. When zinc is added to the synthesis, the photoluminescence quantum yield reaches 3.4 %.

  9. A sulphur isotopic study of the Bleikvassli Zn-Pb-Cu deposit, Nordland, northern Norway

    NASA Astrophysics Data System (ADS)

    Skauli, H.; Boyce, A. J.; Fallick, A. E.

    1992-09-01

    The Bleikvassli Zn-Pb-Cu deposit occurs in the Uppermost Allochthon in the Caledonides of northern Norway. The orebody is enclosed in amphibolite-facies schists and gneisses, underlain by amphibolites, and it has been classified as a sediment-hosted massive sulphide (SEDEX) deposit. The stratiform ore is dominantly pyritic, with a basal layer of pyrrhotitic ore. Sulphide veins occur in the footwall. The orebody generally has a limited range of δ34S, from 0.3 to 4.5% (x = 2.4 ± 1.2‰, 1 σ, n = 26). The lowest δ34S values (0.3 2.3‰) were found in sulphide veins in the footwall and vent proximal stratiform ore. More distal pyritic Zn-Pb ore has heavier average δ34S values (up to 4.5‰). The ore sulphides were deposited from a hydrothermal solution with δ34S about 2‰ perhaps with the incorporation of a minor portion of sulphide from the ambient seawater. The hydrothermal solution probably acquired most of its sulphide from the underlying mixed lithology; notably basaltic rocks. Sulphide produced by thermochemical reduction of seawater in the deep conduit system may also have been incorporated. Bacteriogenic sulphide is not likely as a major source of ore sulphur in the massive ore. Sulphide incorporated in distal pyrite, which have δ34S from -12 to-10‰, could have formed either by oxidation of the hydrothermal sulphide, or by bacterial reduction of seawater sulphate in the depositional environment. Exchange of sulphur isotopes probably took place only on a localized scale during Caledonian metamorphism, the bulk sulphur isotopic composition of the ore being preserved in a hand specimen scale.

  10. Relation of pH and other soil variables to concentrations of Pb, Cu, Zn, Cd, and Se in earthworms

    USGS Publications Warehouse

    Beyer, W.N.; Hensler, G.L.; Moore, J.

    1987-01-01

    Various soil treatments (clay, composted peat, superphosphate, sulfur, calcium carbonate, calcium chloride, zinc chloride, selenous acid) were added to experimental field plots to test the effect of different soil variables on the concentrations of 5 elements in earthworms (Pb, Cu, Zn, Cd, Se). Concentrations of the 5 elements were related to 9 soil variables (soil Pb, soil Cu, soil Zn, pH, organic matter, P, K, Mg, and Ca) with linear multiple regression. Lead concentrations in earthworms were positively correlated with soil Pb and soil organic matter, and negatively correlated with soil pH and soil Mg, with an R2 of 64%. Se concentrations were higher in earthworms from plots amended with Se, and Zn concentrations were higher in earthworms from plots amended with Zn. However, none of the other soil variables had important effects on the concentrations of Cu, Zn, Cd and Se in earthworms. Although some significant statistical relations were demonstrated, the values of r2 of all relations (> 20%) were so low that they had little predictive value.

  11. Band bending at Al, In, Ag, and Pt interfaces with CdTe and ZnTe (110)

    SciTech Connect

    Wahi, A.K.; Miyano, K.; Carey, G.P.; Chiang, T.T.; Lindau, I.; Spicer, W.E. )

    1990-05-01

    Band bending behavior and interfacial chemistry for Al, In, Ag, and Pt overlayers on vacuum-cleaved {ital p}-CdTe and {ital p}-ZnTe (110) have been studied using ultraviolet photoelectron spectroscopy (UPS) and x-ray photoelectron spectroscopy (XPS). These metals provide a range of metal--substrate reactivities: Al reacts strongly with Te, Ag moderately, and In minimally, with no evidence seen for In reaction on ZnTe. Pt exhibits strong alloying behavior with both Cd and Zn. All four metals are found to yield Schottky barriers on CdTe and ZnTe, with a narrow range of final Fermi level positions, {ital E}{sub {ital fi}}={ital E}{sub {ital f}}{minus}{ital E}{sub VBM}, observed on CdTe, from 0.9 to 1.05{plus minus}0.1 eV, and on ZnTe from 0.65 to 1.0{plus minus}0.1 eV. The prediction of the MIGS model that a difference in barrier height exists for two semiconductors dependent upon their band lineup (valence band offset) is examined and found to agree with experiment for Ag, Pt, and Al, but not for In. For the highly reactive Al, no evidence for the overlayer metallicity required for metal-induced gap states (MIGS) to operate is seen on CdTe or ZnTe until after band bending has stabilized. Reaction and intermixing for Al, Ag, and Pt overlayers on CdTe and ZnTe indicate these interfaces are not ideal. The possible role of defects at these four metal/CdTe and metal/ZnTe interfaces is considered, and provides a consistent explanation for the final Fermi level positions observed.

  12. Spatial distribution of gut juice extractable Cu, Pb and Zn in sediments from the Pearl River Estuary, Southern China.

    PubMed

    Wang, Fei; Wang, Wen-Xiong; Huang, Xiao-Ping

    2012-06-01

    In this study, we compared the spatial distribution of total metals (Cu, Pb, and Zn) and bioaccessible metals, which were quantified by incubating sediments with the digestive fluid of sipunculans Sipunculus nudus, in natural sediments of the Pearl River Estuary (PRE). The spatial distribution of bioaccessible metal was not the same as that of total metals in PRE sediments, which were mainly controlled by fine-grained size, total organic carbon (TOC) and Fe. Geochemical factors were important in interpreting this different spatial variation. The similar spatial variations of bioaccessible Cu and total Cu were related to TOC in PRE sediments. Differently from the total Zn, a higher bioaccessible Zn was detected near the West Channel of PRE because of a lower TOC. However, the distribution of bioaccessible Pb was not significantly related to any sediment geochemistry. This study provides a more accurate view of metal pollution in the PRE natural sediments.

  13. Photosensitization of ZnO by AgBr and Ag2CO3: Nanocomposites with tandem n-n heterojunctions and highly enhanced visible-light photocatalytic activity.

    PubMed

    Pirhashemi, Mahsa; Habibi-Yangjeh, Aziz

    2016-07-15

    Facile ultrasonic-irradiation method was applied for photosensitization of ZnO by combining with AgBr and Ag2CO3 particles through preparation of novel ternary nanocomposites. The prepared samples were characterized by XRD, SEM, TEM, EDX, UV-Vis DRS, FT-IR, BET, and PL techniques. Photocatalytic activity was investigated by degradation of rhodamine B under visible-light irradiation. It was found that photocatalytic activity of the ZnO was greatly enhanced by coupling with AgBr and Ag2CO3 particles, as narrow band gap semiconductors, through formation of tandem n-n heterojunctions. The nanocomposite with 20% of Ag2CO3 displayed the highest photocatalytic activity with the degradation rate constants which are nearly 122, 31, and 25 times higher than those of the ZnO, ZnO/AgBr, and ZnO/Ag2CO3 samples, respectively. Moreover, the trapping experiments confirmed that superoxide ion radicals and holes are the main active species responsible for the degradation reaction. Finally, it was also demonstrated that the ternary ZnO/AgBr/Ag2CO3 (20%) nanocomposite has enhanced activity in degradation of methylene blue and methyl orange. Hence, this work shows a great potential of the ternary photocatalyst for purification of contaminated water from organic pollutants.

  14. The evolution of authigenic Zn-Pb-Fe-bearing phases in the Grieves Siding peat, western Tasmania

    NASA Astrophysics Data System (ADS)

    Awid-Pascual, Richelle; Kamenetsky, Vadim S.; Goemann, Karsten; Allen, Neil; Noble, Taryn L.; Lottermoser, Bernd G.; Rodemann, Thomas

    2015-08-01

    A thick peat profile overlying mineralized metasediments possesses exceptionally high base metal contents (up to 28.6 wt% Zn and up to 3.8 wt% Pb) in the form of abundant detrital and authigenic minerals. This metal-rich peat was examined using X-ray diffraction, scanning electron microscopy and Raman spectroscopy to determine the characteristics, mineral associations, phase evolution and conditions of formation of Zn-Pb-Fe-bearing minerals within the peat. Mineral assemblages consisting of sulfides, silicates, sulfates, oxides, carbonates and phosphates could be classified as follows: (1) detrital minerals supplied by the surrounding rocks (i.e., Cambrian volcanics and sediments, Ordovician carbonates) and (2) authigenic phases that are precipitated in situ, including the predominant Zn-Pb-Fe-bearing phases. Detrital minerals are characterized by weathering-related morphologies (e.g., round, smooth surfaces and angular edges and dissolution pits), whereas authigenic phases are recognized by their delicate microparticle textures (e.g., bladed, framboidal and botryoidal textures). Zinc-bearing phases are represented by non-stoichiometric phases, also containing S, C, O and Al; sphalerite, baileychlore and Fe-Zn-Pb carbonate. Authigenic Pb- and Fe-bearing phases are also present in the peat such as galena, anglesite, plumbojarosite, magnetite and pyrite. A "line of descent" of authigenic sulfides has been established, suggesting that a non-stoichiometric, possibly amorphous Zn-rich phase is a precursor to the sphalerite. Stages of pyrite formation, where massive polycrystalline pyrite is produced via disseminated and framboidal pyrite, have also been hypothesized in this study. The assemblages of authigenic minerals in the peat reflect dynamic physical and chemical conditions, including biological processes, and are not necessarily in equilibrium with each other.

  15. Surface plasmon enhanced near-UV emission in monodispersed ZnO:Ag core-shell type nanoparticles synthesized by a wet chemical method

    NASA Astrophysics Data System (ADS)

    Jadhav, J.; Biswas, S.

    2016-03-01

    Monodispersed core-shell type ZnO:Ag nanoparticles were synthesized by a wet chemical method and their salient properties were reported. The synthesis technique explores a facile route following a chemical reaction between aqueous solutions of poly-vinyl alcohol (PVA), sucrose and Zn2+ salt. The Zn2+-PVA-sucrose polymer precursor powders so obtained after the reaction was further explored for the synthesis of ZnO:Ag nanoparticles. The key part of the process lies in the use of polymer encapsulated ZnO nanoparticles as templates to obtain the ZnO core-Ag shell type nanostructures. Structural, morphological and optical properties of the derived ZnO:Ag core-shell nanoparticles were evaluated with X-ray diffraction (XRD), field emission scanning electron microscope (FESEM), high resolution transmission electron microscope (HRTEM), Raman spectroscopy, UV-visible diffuse reflectance spectroscopy, and photoluminescence (PL) spectroscopy. Microstructural analysis revealed monodispersed platelet shaped ZnO nanoparticles with a thin layer of Ag coating on the surface. The surface modified ZnO nanoparticles show colossal enhancement in their near-UV emission characteristics, primarily due to the efficient excitation of surface plasmons and excellent semiconductor-metal interfacing in the ZnO:Ag nanoparticles.

  16. TiInZnO/Ag/TiInZnO multilayer films for transparent conducting electrodes of dye-sensitized solar cells

    NASA Astrophysics Data System (ADS)

    Kim, Ho-Hyeong; Kim, Eun-Mi; Lee, Kyung-Ju; Park, Jae-Young; Lee, Yu-Ri; Shin, Dong-Chan; Hwang, Tae-Jin; Heo, Gi-Seok

    2014-03-01

    Ti-In-Zn-O (TIZO) and TIZO/Ag/TIZO multilayer transparent films were prepared at room temperature on glass substrates using an RF/DC magnetron sputtering system. The optical and electrical properties of the multilayer structures were examined according to the thickness of each TIZO/Ag/TIZO layer. A transparent and conductive film with a sheet resistance of 11.1 Ω/□ and a transmittance of 86.9% at 550 nm (94.2%, normalized to the glass substrate) was obtained at a TIZO/Ag/TIZO thickness of 100/8/42 nm. The TIZO and TIZO/Ag/TIZO multilayer films exhibited higher mechanical resistances against an increasing load of external scratches than the indium tin oxide (ITO) film. Overall, the properties of the TIZO/Ag/TIZO multilayer films were comparable or superior to those of the ITO/Ag/ITO multilayer. The deposited TIZO/Ag/TIZO multilayer films were used in the fabrication of dye-sensitized solar cells (DSSCs) as the transparent electrode. The TIZO/Ag/TIZO multilayer-based DSSCs exhibited a short circuit photocurrent density of 9.4 mA/cm2, a photocurrent of 613 mV, and an overall cell efficiency of 3.1% at a light intensity of one sun.

  17. One-pot facile synthesis of branched Ag-ZnO heterojunction nanostructure as highly efficient photocatalytic catalyst

    NASA Astrophysics Data System (ADS)

    Huang, Qingli; Zhang, Qitao; Yuan, Saisai; Zhang, Yongcai; Zhang, Ming

    2015-10-01

    In this paper, the branched Ag-ZnO heterojunction nanostructure and the branched ZnO were synthesized successfully by a facile, green and one-pot hydrothermal method. Such branched heterojunction and the comparing branched pure ZnO were characterized by X-ray diffraction, field emission scanning electron microscopy (FESEM), high resolution transmission electron microscopy (HRTEM), energy-dispersive spectroscopy (EDS), X-ray photoelectron spectroscopy (XPS), photoluminescence spectroscopy (PL) and UV-vis diffuse reflectance spectra (DRS). The photocatalytic degradation of RhB aqueous solution and acetaldehyde (CH3CHO) gas results both showed that the branched Ag-ZnO heterojunction possessed the enhanced photocatalytic properties in comparison to the branched ZnO and Ag-ZnO counterparts due to its special interface structures and fast separation of its photogenerated charge carriers. This method is simple, feasible and can provide an important clue for synthesis and application of other branched metal/semiconductor heterojunction nanostructures.

  18. Similarities and Differences between the Sandstone-Hosted Jinding Zn-Pb Deposit and MVT Deposits

    NASA Astrophysics Data System (ADS)

    Chi, G.; Xue, C.

    2009-05-01

    The Jinding Zn-Pb deposit (Lanping basin, Yunnan, China) is the largest sandstone-hosted Zn-Pb deposit in the world, having a total reserve of approximately 220 Mt of ore grading 6.1% Zn and 1.3 Pb%. The sedimentary rocks in the Lanping basin were formed in continental environments and were subject to strong deformation during the Himalayan orogeny. The orebodies are hosted in Cretaceous and Paleocene sandstones and pebbly sandstones which formed a structural dome (the Jinding dome) near a regional, high- angle normal fault (the Pijiang fault). The ores can be divided into two types, the sandstone-type and breccia- type. The former consists of fine-grained sphalerite-galena-pyrite-marcasite disseminations in sandstones, and the latter includes sphalerite-galena-pyrite-marcasite disseminations in the matrix and celestite-pyrite- marcasite-sphalerite-galena-calcite filling fractures and cavities. Colloform textures are common in the breccia-type ores, which are associated with sand veins or dykes cemented by sulfides. Breccia-type ores commonly contain solid bitumen, and freshly opened sandstone-type ores have an oily smell. Oil inclusions are common in both types of ores. CO2-CH4-light hydrocarbon inclusions were found in celestite, sphalerite, authigenic quartz, and calcite. Homogenization temperatures of aqueous inclusions range from about 60 to 300 degree C, and salinities range from 1 to 25 wt.% NaCl equivalent. There is a trend of decreasing temperature and increasing salinities away from the Pijiang fault. Delta 34S (CDT) of sulfides range from -32 to 0 per mil. Noble gas isotopes of fluid inclusions and Pb isotopes of sulfides indicate both mantle and crustal sources. It is proposed that the mineralization resulted from mixing between a high-temperature, low-salinity, deep-seated fluid and a relatively high-salinity, low-temperature, basinal fluid. The former ascended along the Pijiang fault and spread westward, and the latter migrated before and during

  19. Ag-nanoparticle-decorated porous ZnO-nanosheets grafted on a carbon fiber cloth as effective SERS substrates

    NASA Astrophysics Data System (ADS)

    Wang, Zhiwei; Meng, Guowen; Huang, Zhulin; Li, Zhongbo; Zhou, Qitao

    2014-11-01

    We report on the large-scale synthesis of Ag-nanoparticle (Ag-NP) decorated ZnO-mesoporous-nanosheets (NSs) grafted on a flexible carbon fiber cloth (CFC), as sensitive and reproducible surface enhanced Raman scattering (SERS) substrates with excellent flexibility. The composite SERS-substrates are achieved by a combination of atomic layer deposition of ZnO-seeds on each fiber of the CFC (denoted as ZnO-seeds@CFC), chemical bath deposition and subsequent pyrolysis for the creation of ZnO-mesoporous-NSs grafted on ZnO-seeds@CFC, and ion-sputtering of Ag-NPs on the ZnO-mesoporous-NSs. As abundant SERS ``hot spots'' are generated from the electromagnetic coupling of the densely distributed Ag-NPs, and the semiconducting ZnO-mesoporous-NSs also have chemical supporting enhancement and distinct molecule adsorbing abilities, the composite SERS-substrates demonstrate high SERS-sensitivity with good signal reproducibility. As a trial for potential applications, the composite SERS-substrates were used to identify pesticides and highly toxic polychlorinated biphenyls (PCBs), and low concentrations down to 10-7 M for methyl parathion and 5 × 10-6 M for PCB-77 were reached, respectively, showing promising potential for the SERS-based rapid detection of toxic organic pollutants in the environment.We report on the large-scale synthesis of Ag-nanoparticle (Ag-NP) decorated ZnO-mesoporous-nanosheets (NSs) grafted on a flexible carbon fiber cloth (CFC), as sensitive and reproducible surface enhanced Raman scattering (SERS) substrates with excellent flexibility. The composite SERS-substrates are achieved by a combination of atomic layer deposition of ZnO-seeds on each fiber of the CFC (denoted as ZnO-seeds@CFC), chemical bath deposition and subsequent pyrolysis for the creation of ZnO-mesoporous-NSs grafted on ZnO-seeds@CFC, and ion-sputtering of Ag-NPs on the ZnO-mesoporous-NSs. As abundant SERS ``hot spots'' are generated from the electromagnetic coupling of the densely

  20. LED Die-Bonded on the Ag/Cu Substrate by a Sn-BiZn-Sn Bonding System

    NASA Astrophysics Data System (ADS)

    Tang, Y. K.; Hsu, Y. C.; Lin, E. J.; Hu, Y. J.; Liu, C. Y.

    2016-08-01

    In this study, light emitting diode (LED) chips were die-bonded on a Ag/Cu substrate by a Sn-BixZn-Sn bonding system. A high die-bonding strength is successfully achieved by using a Sn-BixZn-Sn ternary system. At the bonding interface, there is observed a Bi-segregation phenomenon. This Bi-segregation phenomenon solves the problems of the brittle layer-type Bi at the joint interface. Our shear test results show that the bonding interface with Bi-segregation enhances the shear strength of the LED die-bonding joints. The Bi-0.3Zn and Bi-0.5Zn die-bonding cases have the best shear strength among all die-bonding systems. In addition, we investigate the atomic depth profile of the deposited Bi-xZn layer by evaporating Bi-xZn E-gun alloy sources. The initial Zn content of the deposited Bi-Zn alloy layers are much higher than the average Zn content in the deposited Bi-Zn layers.

  1. Controllable synthesis and adjustable antineoplastic activity of bovine serum albumin-conjugated PbS/Ag2S core/shell nano-composites.

    PubMed

    Wang, Hua-Jie; Yu, Xue-Hong; Cao, Ying; Zhou, Bei; Wang, Cai-Feng

    2012-08-01

    Series of mono-dispersed bovine serum albumin (BSA)-conjugated PbS/Ag(2)S core/shell nano-composites with different Pb/Ag ratios had been successfully synthesized by an ion-exchange method under the gentle conditions using BSA-conjugated PbS nano-crystals as precursors, which were prepared by a biomimetic method. Fourier transform infrared spectra analysis and transmission electron microscopy (TEM) observation demonstrated that BSA was a key factor to control the morphology and size of final products. Additionally, the real-time TEM observation, X-ray powder diffraction and atomic absorption spectroscopy analysis were applied to monitor the synthesis process. The results indicated that the shell thickness and ratio of Pb to Ag could be controlled by adjusting the ion-exchange time. Both metabolic and morphological methods revealed that the proliferation of rat pheochromocytoma (PC 12) cells could be inhibited by BSA-conjugated PbS/Ag(2)S core/shell nano-composites, and the antineoplastic activity was Pb/Ag ratio-dependent. It might be explained by a Trojan horse-type mechanism. Summarily, the present study would be helpful to find a new core/shell nano-composite with higher and controllable antineoplastic activity due to the synergistic reaction of different metal ions.

  2. Selective photochemical synthesis of Ag nanoparticles on position-controlled ZnO nanorods for the enhancement of yellow-green light emission

    NASA Astrophysics Data System (ADS)

    Park, Hyeong-Ho; Zhang, Xin; Lee, Keun Woo; Sohn, Ahrum; Kim, Dong-Wook; Kim, Joondong; Song, Jin-Won; Choi, Young Su; Lee, Hee Kwan; Jung, Sang Hyun; Lee, In-Geun; Cho, Young-Dae; Shin, Hyun-Beom; Sung, Ho Kun; Park, Kyung Ho; Kang, Ho Kwan; Park, Won-Kyu; Park, Hyung-Ho

    2015-12-01

    A novel technique for the selective photochemical synthesis of silver (Ag) nanoparticles (NPs) on ZnO nanorod arrays is established by combining ultraviolet-assisted nanoimprint lithography (UV-NIL) for the definition of growth sites, hydrothermal reaction for the position-controlled growth of ZnO nanorods, and photochemical reduction for the decoration of Ag NPs on the ZnO nanorods. During photochemical reduction, the size distribution and loading of Ag NPs on ZnO nanorods can be tuned by varying the UV-irradiation time. The photochemical reduction is hypothesized to facilitate the adsorbed citrate ions on the surface of ZnO, allowing Ag ions to preferentially form Ag NPs on ZnO nanorods. The ratio of visible emission to ultraviolet (UV) emission for the Ag NP-decorated ZnO nanorod arrays, synthesized for 30 min, is 20.5 times that for the ZnO nanorod arrays without Ag NPs. The enhancement of the visible emission is believed to associate with the surface plasmon (SP) effect of Ag NPs. The Ag NP-decorated ZnO nanorod arrays show significant SP-induced enhancement of yellow-green light emission, which could be useful in optoelectronic applications. The technique developed here requires low processing temperatures (120 °C and lower) and no high-vacuum deposition tools, suitable for applications such as flexible electronics.A novel technique for the selective photochemical synthesis of silver (Ag) nanoparticles (NPs) on ZnO nanorod arrays is established by combining ultraviolet-assisted nanoimprint lithography (UV-NIL) for the definition of growth sites, hydrothermal reaction for the position-controlled growth of ZnO nanorods, and photochemical reduction for the decoration of Ag NPs on the ZnO nanorods. During photochemical reduction, the size distribution and loading of Ag NPs on ZnO nanorods can be tuned by varying the UV-irradiation time. The photochemical reduction is hypothesized to facilitate the adsorbed citrate ions on the surface of ZnO, allowing Ag ions to

  3. A survey of Pb, Cu, Zn, Cd, Cr, As, and Se in earthworms and soil from diverse sites.

    PubMed

    Beyer, W N; Cromartie, E J

    1987-01-01

    Earthworms and soils were collected from 20 diverse sites in Maryland, Pennsylvania, and Virginia, and were analyzed for Pb, Cu, Zn, Cd, Cr, As, and Se. Correlation coefficients relating concentrations of the elements in earthworms to concentrations in soil were low (-0.20Pb (2100 ppm), Zn (1600 ppm), Cd (23 ppm) and Se (7.6 ppm) detected in earthworms were in the range reported to be toxic to animals fed diets containing these elements; however, even in the absence of any environmental contamination, some species of earthworms may contain high concentrations of Pb, Zn, and Se. Earthworms of the genus Eisenoides, for example, were exceptional in their ability to concentrate Pb. When earthworms are used as indicators of environmental contamination, it is important to identify the species, to report the soil characteristics, and to collect similar earthworms from very similar but uncontaminated soil. PMID:24253769

  4. A survey of Pb, Cu, Zn, Cd, Cr, As, and Se in earthworms and soil from diverse sites

    USGS Publications Warehouse

    Beyer, W.N.; Cromartie, E.J.

    1987-01-01

    Earthworms and soils were collected from 20 diverse sites in Maryland, Pennsylvania, and Virginia, and were analyzed for Pb, Cu, Zn, Cd, Cr, As, and Se. Correlation coefficients relating Iconcentrations of the elements in earthworms to concentrations in soil were low (-0.20Pb (2100 ppm), Zn (1600 ppm), Cd (23 ppm) and Se (7.6 ppm) detected in earthworms were in the range reported to be toxic to animals fed diets containing these elements; however, even in the absence of any environmental contamination, some species of earthworms may contain high concentrations of Pb, Zn, and Se. Earthworms of the genus Eisenoides, for example, were exceptional in their ability to concentrate Pb. When earthworms are used as indicators of environmental contamination, it is important to identify the species, to report the soil characteristics, and to collect similar earthworms from very similar but uncontaminated soil.

  5. In Situ Fabrication of 3D Ag@ZnO Nanostructures for Microfluidic Surface-Enhanced Raman Scattering Systems

    PubMed Central

    2015-01-01

    In this work, we develop an in situ method to grow highly controllable, sensitive, three-dimensional (3D) surface-enhanced Raman scattering (SERS) substrates via an optothermal effect within microfluidic devices. Implementing this approach, we fabricate SERS substrates composed of Ag@ZnO structures at prescribed locations inside microfluidic channels, sites within which current fabrication of SERS structures has been arduous. Conveniently, properties of the 3D Ag@ZnO nanostructures such as length, packing density, and coverage can also be adjusted by tuning laser irradiation parameters. After exploring the fabrication of the 3D nanostructures, we demonstrate a SERS enhancement factor of up to ∼2 × 106 and investigate the optical properties of the 3D Ag@ZnO structures through finite-difference time-domain simulations. To illustrate the potential value of our technique, low concentrations of biomolecules in the liquid state are detected. Moreover, an integrated cell-trapping function of the 3D Ag@ZnO structures records the surface chemical fingerprint of a living cell. Overall, our optothermal-effect-based fabrication technique offers an effective combination of microfluidics with SERS, resolving problems associated with the fabrication of SERS substrates in microfluidic channels. With its advantages in functionality, simplicity, and sensitivity, the microfluidic-SERS platform presented should be valuable in many biological, biochemical, and biomedical applications. PMID:25402207

  6. Insights into the proteomic response of soybean towards Al₂O₃, ZnO, and Ag nanoparticles stress.

    PubMed

    Hossain, Zahed; Mustafa, Ghazala; Sakata, Katsumi; Komatsu, Setsuko

    2016-03-01

    Understanding the complex mechanisms involved in plant response to nanoparticles is indispensable in assessing the impact of nano-pollutants on environment. The present study compares the phytotoxicity of three different metal-based nanoparticles (Al2O3, ZnO, and Ag) in soybean seedling at proteome level. Plant growth, rigidity of roots, and root cell viability were markedly affected by ZnO- and Ag-NPs stress; while, Al2O3-NPs challenged soybean maintained normal seedling growth like control. Moreover, severe oxidative burst was evident in ZnO-NPs and Ag-NPs treatments. Gel-free proteomic analysis of NPs stressed soybean roots revealed 104 commonly changed proteins primarily associated with secondary metabolism, cell organization, and hormone metabolism. Oxidation-reduction cascade related genes, such as GDSL motif lipase 5, SKU5 similar 4, galactose oxidase, and quinone reductase were up-regulated in Al2O3-NPs challenged roots and down-regulated in ZnO- and Ag-NPs treatments. In comparison to root, 16 common proteins were found to be significantly changed in leaves of NPs exposed soybean that were predominantly associated to photosystem and protein degradation. The proteomic findings suggest that high abundance of proteins involved in oxidation-reduction, stress signaling, hormonal pathways related to growth and development might be the principal key for optimum growth of soybean under Al2O3-NPs stress.

  7. Synthesis of ZnS:Ag,Co water-soluble blue afterglow nanoparticles and application in photodynamic activation

    NASA Astrophysics Data System (ADS)

    Ma, Lun; Zou, Xiaoju; Hossu, Marius; Chen, Wei

    2016-08-01

    Silver and cobalt co-doped ZnS (ZnS:Ag,Co) water-soluble afterglow nanoparticles were synthesized using a wet chemistry method followed by aging at room temperature. The nanoparticles had a cubic zinc blende structure with average sizes of approximately 4 nm and emitted a blue fluorescence emission centered at 441 nm due to radiative transitions from surface defects to Ag+ luminescent centers. Intense afterglow emission peaking at 475 nm from the obtained nanoparticles was observed and was red-shifted compared to the fluorescence emission peak. X-ray photoelectron spectroscopy revealed a large increase of O/S ratio, indicating a surface oxidation process during aging. The S vacancies produced accordingly may contribute to form more electron traps and enhance afterglow. The ZnS:Ag,Co afterglow nanoparticles have a very low dark-toxicity and are applied as a light source for photodynamic therapy activation by conjugating with protoporphyrin together. Our preliminary study has shown that the ZnS:Ag,Co afterglow nanoparticles can significantly reduce the x-ray dosage used in activation and thus may be a very promising candidate for future x-ray excited photodynamic therapy in deep cancer treatment.

  8. The world-class Jinding Zn-Pb deposit: ore formation in an evaporite dome, Lanping Basin, Yunnan, China

    NASA Astrophysics Data System (ADS)

    Leach, David L.; Song, Yu-Cai; Hou, Zeng-Qian

    2016-07-01

    The Jinding Zn-Pb sediment-hosted deposit in western Yunnan, China, is the fourth largest Zn deposit in Asia. Based on field observations of the ore textures, breccias, and the sandstone host rocks, the ores formed in a dome that was created by the diapiric migration of evaporites in the Lanping Basin during Paleogene deformation and thrust loading. Most of the ore occurs in sandstones that are interpreted to be a former evaporite glacier containing a mélange of extruded diapiric material, including breccias, fluidized sand, and evaporites that mixed with sediment from a fluvial sandstone system. A pre-ore hydrocarbon and reduced sulfur reservoir formed in the evaporite glacier that became the chemical sink for Zn and Pb in a crustal-derived metalliferous fluid. In stark contrast to previous models, the Jinding deposit does not define a unique class of ore deposits; rather, it should be classified as MVT sub-type hosted in a diapiric environment. Given that Jinding is a world-class ore body, this new interpretation elevates the exploration potential for Zn-Pb deposit in other diapir regions in the world.

  9. Bioaccessibility of Cd, Cu, Fe, Mn, Pb, and Zn in hazelnut and walnut kernels investigated by an enzymolysis approach.

    PubMed

    Arpadjan, Sonja; Momchilova, Svetlana; Venelinov, Tony; Blagoeva, Elitsa; Nikolova, Magdalena

    2013-06-26

    Bioaccessibility of four essential (Fe, Cu, Mn, Zn) and two toxic (Cd, Pb) elements in kernels of four walnut and four hazelnut cultivars was investigated using sequential enzymolysis approach and atomic absorption spectrometry. It was found that the assimilable part of elements was not dependent on nut cultivar. The bioaccessible fraction of Cu, Mn, and Zn was definitely higher for hazelnuts (62% Cu, 39% Mn, 58% Zn) than for walnuts (14% Cu, 21% Mn, 15% Zn). Bioaccessible Fe was 20-24% from its total content for both nut types. Solubility in the simulated intestinal juice is affected by both formation of stable soluble complexes and back sorption of dissolved elements on nut solid residues. Lead shows strong insolubility due to the high sorption affinity of lead ions to the insoluble fraction of nuts. Thus, walnuts and hazelnuts could act as effective biosorbents for lead detoxication.

  10. Increasing photon absorption and stability of PbS quantum dot solar cells using a ZnO interlayer

    SciTech Connect

    Lai, Lai-Hung; Speirs, Mark J.; Loi, Maria A.; Chang, Feng-Kuei; Chen, Jen-Sue; Piveteau, Laura; Kovalenko, Maksym V.; Wu, Jih-Jen

    2015-11-02

    We compared PbS quantum dot (QD) solar cells with different cathode interlayer materials, namely, LiF and ZnO nanoparticles, using the same device structure. Solar cells fabricated with the ZnO interlayer gave a power conversion efficiency of 4.8%, which is higher (above the experimental variation) than the 4.1% efficiency obtained with a LiF interlayer. We found that the ZnO interlayer alters the spatial distribution of the optical field, leading to an increase in external quantum efficiency in the visible range. Furthermore, devices with ZnO as interlayer showed more stable performance than the ones using LiF, with practically no power conversion efficiency degradation after 1 month inside a N{sub 2} glovebox.

  11. Geochemical position of Pb, Zn and Cd in soils near the Olkusz mine/smelter, South Poland: effects of land use, type of contamination and distance from pollution source.

    PubMed

    Chrastný, Vladislav; Vaněk, Aleš; Teper, Leslaw; Cabala, Jerzy; Procházka, Jan; Pechar, Libor; Drahota, Petr; Penížek, Vít; Komárek, Michael; Novák, Martin

    2012-04-01

    The soils adjacent to an area of historical mining, ore processing and smelting activities reflects the historical background and a mixing of recent contamination sources. The main anthropogenic sources of metals can be connected with historical and recent mine wastes, direct atmospheric deposition from mining and smelting processes and dust particles originating from open tailings ponds. Contaminated agriculture and forest soil samples with mining and smelting related pollutants were collected at different distances from the source of emission in the Pb-Zn-Ag mining area near Olkusz, Upper Silesia to (a) compare the chemical speciation of metals in agriculture and forest soils situated at the same distance from the point source of pollution (paired sampling design), (b) to evaluate the relationship between the distance from the polluter and the retention of the metals in the soil, (c) to describe mineralogy transformation of anthropogenic soil particles in the soils, and (d) to assess the effect of deposited fly ash vs. dumped mining/smelting waste on the mobility and bioavailability of metals in the soil. Forest soils are much more affected with smelting processes than agriculture soils. However, agriculture soils suffer from the downward metal migration more than the forest soils. The maximum concentrations of Pb, Zn, and Cd were detected in a forest soil profile near the smelter and reached about 25 g kg(- 1), 20 g kg(- 1) and 200 mg kg(- 1) for Pb, Zn and Cd, respectively. The metal pollutants from smelting processes are less stable under slightly alkaline soil pH then acidic due to the metal carbonates precipitation. Metal mobility ranges in the studied forest soils are as follows: Pb > Zn ≈ Cd for relatively circum-neutral soil pH (near the smelter), Cd > Zn > Pb for acidic soils (further from the smelter). Under relatively comparable pH conditions, the main soil properties influencing metal migration are total organic carbon and cation exchange

  12. Theoretical and experimental investigation of doping M in ZnSe (M = Cd, Mn, Ag, Cu) clusters: optical and bonding characteristics.

    PubMed

    Xu, Shuhong; Xu, Xiaojing; Wang, Chunlei; Zhao, Zengxia; Wang, Zhuyuan; Cui, Yiping

    2016-03-01

    The optical and bonding characteristics of doping ZnSe quantum dots (QDs) were investigated. Cd-, Mn-, Ag- and Cu-doped ZnSe were synthesized in aqueous solution. Theoretically, the intensity of the Cd-Se bond was similar to that of the Zn-Se bond, which illustrates that Cd can be doped into ZnSe materials at any ratio. We found that Mn-Se bonding was stronger than Zn-Se bonding. Ag-doped ZnSe nanoclusters show the same bonding and configuration as Cu-doped ZnSe. Moreover, Cd can be doped into ZnSe using both the substitution- and vacancy-doping method. For Mn-doped ZnSe clusters, small amounts of Mn impurity lead to stronger bonding with Se, but larger amounts of Mn impurity led to the formation of a Mn-Mn metal bond. The theoretical results show that it is difficult to form a vacancy-doping cluster for Mn-doped ZnSe materials. In experiments, the absorption and photoluminescence (PL) spectral wavelengths of Mn-doped ZnSe nanocrystals were the same as those of pure ZnSe nanocrystals, showing that the Mn impurity is not doped into ZnSe nanocrystals. Ag- and Cu-doped ZnSe nanocrystals have the same PL characteristics. The doping of an impurity is related to the solubility product, and not the bonding intensity.

  13. Ultrasensitive SERS detection of trinitrotoluene through capillarity-constructed reversible hot spots based on ZnO-Ag nanorod hybrids

    NASA Astrophysics Data System (ADS)

    He, Xuan; Wang, Hui; Li, Zhongbo; Chen, Dong; Liu, Jiahui; Zhang, Qi

    2015-04-01

    A simple and efficient self-approach strategy was used to apply ultrasensitivity and self-revive ZnO-Ag hybrid surface-enhanced Raman scattering (SERS) sensors for the highly sensitive and selective detection of explosive TNT in both solution and vapour conditions. The good ultrasensitive sensing performance is a result of the abundant Raman hot spots, which were spontaneously formed in a reversible way by the self-approaching of flexible ZnO-Ag hybrid nanorods driven by the capillary force of solvent evaporation. Moreover, the enhancement effect was repeatedly renewed by the reconstruction of molecular bridges, which could selectively detect TNT with a lower limit of 4 × 10-14 M. In addition, TNT vapor was also tested under this sensor, whereby once the ZnO-Ag NRs hybrid substrate was dipped in TNT, this substrate could detect the existence of TNT even in 5 detection cycles via a capillarity-constructed reversible hot spots approach. Compared with other pure Ag-based SERS sensors, this ZnO-Ag hybrid SERS sensor could rapidly self-revive SERS-activity by simple UV light irradiation and could retain stable SERS sensitivity for one month when used for TNT detection. This stable and ultrasensitive SERS substrate demonstrates a new route to eliminate the oxidized inactive problem of traditional Ag-based SERS substrates and suggests promising use in the applications of such hybrids as real-time online sensors for explosives detection.A simple and efficient self-approach strategy was used to apply ultrasensitivity and self-revive ZnO-Ag hybrid surface-enhanced Raman scattering (SERS) sensors for the highly sensitive and selective detection of explosive TNT in both solution and vapour conditions. The good ultrasensitive sensing performance is a result of the abundant Raman hot spots, which were spontaneously formed in a reversible way by the self-approaching of flexible ZnO-Ag hybrid nanorods driven by the capillary force of solvent evaporation. Moreover, the enhancement

  14. Mechanical, structural and thermal properties of Ag-Cu and ZnO reinforced polylactide nanocomposite films.

    PubMed

    Ahmed, Jasim; Arfat, Yasir Ali; Castro-Aguirre, Edgar; Auras, Rafael

    2016-05-01

    Plasticized polylactic acid (PLA) based nanocomposite films were prepared by incorporating polyethylene glycol (PEG) and two selected nanoparticles (NPs) [silver-copper (Ag-Cu) alloy (<100 nm) and zinc oxide (ZnO) (<50 and <100 nm)] through solvent casting method. Incorporation of Ag-Cu alloy into the PLA/PEG matrix increased the glass transition temperature (Tg) significantly. The crystallinity of the nanocomposites (NCs) was significantly influenced by NP incorporation as evidenced from differential scanning calorimetry (DSC) and X-ray diffraction (XRD) analysis. The PLA nanocomposite reinforced with NPs exhibited much higher tensile strength than that of PLA/PEG blend. Melt rheology of NCs exhibited a shear-thinning behavior. The mechanical property drastically reduced with a loading of NPs, which is associated with degradation of PLA. SEM micrographs exhibited that both Ag-Cu alloy and ZnO NPs were dispersed well in the PLA film matrix. PMID:26893045

  15. Impact of spiked concentrations of Cd, Pb, As and Zn in growth medium on elemental uptake of Nasturtium officinale (Watercress).

    PubMed

    Gounden, Denisha; Kisten, Kimona; Moodley, Roshila; Shaik, Shakira; Jonnalagadda, Sreekantha B

    2016-01-01

    This study is aimed at investigating the impact of water quality on the uptake and distribution of three non-essential and toxic elements, namely, As, Cd and Pb in the watercress plant to assess for metal toxicity. The plant was hydroponically cultivated under greenhouse conditions, with the growth medium being spiked with varying concentrations of As, Cd and Pb. Plants that were harvested weekly for elemental analysis showed physiological and morphological symptoms of toxicity on exposure to high concentrations of Cd and Pb. Plants exposed to high concentrations of As did not survive and the threshold for As uptake in watercress was established at 5 ppm. Translocation factors were low in all cases as the toxic elements accumulated more in the roots of the plant than the edible leaves. The impact of Zn on the uptake of toxic elements was also evaluated and Zn was found to have an antagonistic effect on uptake of both Cd and Pb with no notable effect on uptake of As. The findings indicate that phytotoxicity or death of the watercress plant would prevent it from being a route of human exposure to high concentrations of As, Cd and Pb in the environment. PMID:26479037

  16. Impact of spiked concentrations of Cd, Pb, As and Zn in growth medium on elemental uptake of Nasturtium officinale (Watercress).

    PubMed

    Gounden, Denisha; Kisten, Kimona; Moodley, Roshila; Shaik, Shakira; Jonnalagadda, Sreekantha B

    2016-01-01

    This study is aimed at investigating the impact of water quality on the uptake and distribution of three non-essential and toxic elements, namely, As, Cd and Pb in the watercress plant to assess for metal toxicity. The plant was hydroponically cultivated under greenhouse conditions, with the growth medium being spiked with varying concentrations of As, Cd and Pb. Plants that were harvested weekly for elemental analysis showed physiological and morphological symptoms of toxicity on exposure to high concentrations of Cd and Pb. Plants exposed to high concentrations of As did not survive and the threshold for As uptake in watercress was established at 5 ppm. Translocation factors were low in all cases as the toxic elements accumulated more in the roots of the plant than the edible leaves. The impact of Zn on the uptake of toxic elements was also evaluated and Zn was found to have an antagonistic effect on uptake of both Cd and Pb with no notable effect on uptake of As. The findings indicate that phytotoxicity or death of the watercress plant would prevent it from being a route of human exposure to high concentrations of As, Cd and Pb in the environment.

  17. Rapid and nondestructive measurement of labile Mn, Cu, Zn, Pb and As in DGT by using field portable-XRF.

    PubMed

    Chen, Zheng; Williams, Paul N; Zhang, Hao

    2013-09-01

    The technique of diffusive gradients in thin films (DGT) is often employed to quantify labile metals in situ; however, it is a challenge to perform the measurements in-field. This study evaluated the capability of field-portable X-ray fluorescence (FP-XRF) to swiftly generate elemental speciation information with DGT. Biologically available metal ions in environmental samples passively preconcentrate in the thin films of DGT devices, providing an ideal and uniform matrix for XRF nondestructive detection. Strong correlation coefficients (r > 0.992 for Mn, Cu, Zn, Pb and As) were obtained for all elements during calibration. The limits of quantitation (LOQ) for the investigated elements of FP-XRF on DGT devices are 2.74 for Mn, 4.89 for Cu, 2.89 for Zn, 2.55 for Pb, and 0.48 for As (unit: μg cm(-2)). When Pb and As co-existed in the solution trials, As did not interfere with Pb detection when using Chelex-DGT. However, there was a significant enhancement of the Pb reading attributed to As when ferrihydrite binding gels were tested, consistent with Fe-oxyhydroxide surfaces absorbing large quantities of As. This study demonstrates the value of the FP-XRF technique to rapidly and nondestructively detect the metals accumulated in DGT devices, providing a new and simple diagnostic tool for on-site environmental monitoring of labile metals/metalloids.

  18. Facilitation of Pb-Zn mineralisation by diatremes in the Irish Orefield?

    NASA Astrophysics Data System (ADS)

    Elliott, H. A.; Gernon, T. M.; Roberts, S.; Redmond, P.

    2013-12-01

    The Limerick Basin in southwest Ireland is an important part of the Pb-Zn Orefield within the Irish Midlands [1]. A recently discovered cluster of basaltic diatremes within the Stonepark area, spatially associated with mineralization, challenges previously accepted theories that the carbonate hosted Pb-Zn deposits were not related to Lower Carboniferous volcanics within the area. Thus, the genetic relationship between mineralization and magmatism is poorly understood and highly controversial. The diatremes emplaced into the Lower Carboniferous carbonate stratigraphy, are attributed to increased heat flow and magmatism during extensional tectonic activity in the Tournasian [2]. The preferred NE-SW trend of diatremes suggests that they might have been fault controlled. In close proximity to the diatremes a series of extra-crater basaltic lava flows and pyroclastics (Knockroe Formation) is commonly interbedded with argillaceous and crinoidal limestones formed in a shallow marine environment (Lough Gur Formation) [3]. Analysis of trace elements from juvenile material from both the extra-crater and diatreme deposits have confirmed that the two are related, following a broadly linear fractionation trend. The Knockroe sequence is likely sourced from the diatreme eruptions, apparently thickening toward the diatremes, and share compositional and textural similarities with the diatremes. The deposits record at least two different magmatic phases, the first contains fragmented crystals and a very low degree of vesiculation. The second contains no phenocrysts; the lapilli are more altered and have a higher vesicularity (21-42 area %). The low vesicularity of juvenile lapilli (5-26 area %), interbedding of diatreme-sourced Knockroe pyroclastic material and shallow marine deposits, and other large-scale geological relationships indicate that the eruptions were largely phreatomagmatic. However, the occurrence of highly vesiculated lapilli and late stage crosscutting dykes

  19. Antifungal Activity of Ag(I) and Zn(II) Complexes of Sulfacetamide Derivatives

    PubMed Central

    Supuran, Claudiu T.

    2000-01-01

    Reaction of sulfacetamide with arylsulfonyl isocyanates afforded a series of derivatives which were used as ligands (as conjugate bases) for the preparation of metal complexes containing Ag(I) and Zn(II). The newly synthesized complexes, unlike the free ligands, act as effective antifungal agents against Aspergillus and Candida spp., some of them showing activities comparable to ketoconazole, with minimum inhibitory concentrations in the range of 0.3 – 0.5 μg/mL. The mechanism of antifungal action of these complexes seems to be not connected with the inhibition of lanosterol-14-α-demethylase, since the levels of sterols assessed in the fungi cultures were equal in the absence or in the presence of the tested compounds. Probably the new complexes act as inhibitors of phosphomannose isomerase, a key enzyme in the biosynthesis of yeast cell walls. PMID:18475922

  20. Composition dependence of the photochemical reduction of Ag+ by as-grown Pb(ZrxTi1-x)O3 films on indium tin oxide electrode

    NASA Astrophysics Data System (ADS)

    Zhang, Man; Jiang, Chunxiang; Dong, Wen; Zheng, Fengang; Fang, Liang; Su, Xiaodong; Shen, Mingrong

    2013-09-01

    Photochemical growth of metal particles on ferroelectric films has usually been found to depend on polarization effect solely. This research exploits the interplay of the film/electrode interface barrier and depolarization field on the photoreduction of Ag+ to Ag onto Pb(Zr,Ti)O3 (PZT) films deposited on indium tin oxide (ITO) electrodes. Ag nanoparticles are observed on the as-grown polycrystalline PZT films without poling, while the particle size and density are closely related to the concentration of Zr in PZT and the poling direction. The enhancement on the photoelectrochemical properties of the ITO/PZT photocathode by the decoration of Ag nanoparticles is finally demonstrated.

  1. EFFECT OF Sn AND Pb ADDITIONS ON MICROSTRUCTURE OF Mg-6Al-1Zn AS-CAST MAGNESIUM ALLOYS

    NASA Astrophysics Data System (ADS)

    Hou, Haibo; Zhu, Tianping; Wang, Yuxin; Gao, Wei

    2013-07-01

    Much attention has been paid to Mg alloys given that Mg alloys are the most promising lightweight metallic material. They have found applications in automobile and other fields where weight saving is of great significance. Mg-Al-Zn alloy system (AZ series), including AZ91 and AZ61 Mg alloys, is widely used in industry. We have studied the enhancement of mechanical properties by adding alloying elements Sn and Pb. This paper reports our study on the microstructure and element distribution of the alloys with small amounts of tin (Sn) and lead (Pb) additions.

  2. Removal of As, Cd, Cu, Ni, Pb, and Zn from a highly contaminated industrial soil using surfactant enhanced soil washing

    NASA Astrophysics Data System (ADS)

    Torres, Luis G.; Lopez, Rosario B.; Beltran, Margarita

    Surfactant enhanced soil washing (SESW) was applied to an industrial contaminated soil. A preliminary characterization of the soil regarding the alkaline-earth metals, Na, K, Ca and Mg took values of 2866, 2036, 2783 and 4149 mg/kg. The heavy metals As, Cd, Cu, Pb, Ni and Zn, had values of 4019, 14, 35582, 70, 2603, and 261 mg/kg, respectively. When using different surfactants, high removal of Cu, Ni and Zn were found, and medium removals for Pb, As and Cd. In the case of these three metals, tap water removed more than the surfactant solutions, except for the case of As. There were surfactants with average removals (this is, the removal for all the metals studied) of 67.1% (Tween 80), 64.9% (Surfacpol 14104) and 61.2% (Emulgin W600). There were exceptional removals using Texapon N-40 (83.2%, 82.8% and 86.6% for Cu, Ni and Zn), Tween 80 (85.9, 85.4 and 81.5 for Cd, Zn and Cu), Polafix CAPB (79%, 83.2% and 49.7% for Ni, Zn and As). The worst results were obtained with POLAFIX LO with a global removal of 45%, well below of the average removal with tap water (50.2%).All removal efficiencies are reported for a one step washing using 0.5% surfactant solutions, except for the case of mezquite gum, where a 0.1% solution was employed.

  3. Modifying the Surface of a Rashba-Split Pb-Ag Alloy Using Tailored Metal-Organic Bonds

    NASA Astrophysics Data System (ADS)

    Stadtmüller, Benjamin; Seidel, Johannes; Haag, Norman; Grad, Lisa; Tusche, Christian; van Straaten, Gerben; Franke, Markus; Kirschner, Jürgen; Kumpf, Christian; Cinchetti, Mirko; Aeschlimann, Martin

    2016-08-01

    Hybridization-related modifications of the first metal layer of a metal-organic interface are difficult to access experimentally and have been largely neglected so far. Here, we study the influence of specific chemical bonds (as formed by the organic molecules CuPc and PTCDA) on a Pb-Ag surface alloy. We find that delocalized van der Waals or weak chemical π -type bonds are not strong enough to alter the alloy, while localized σ -type bonds lead to a vertical displacement of the Pb surface atoms and to changes in the alloy's surface band structure. Our results provide an exciting platform for tuning the Rashba-type spin texture of surface alloys using organic molecules.

  4. Factors Affecting the Morphology of Pb-Based Glass Frit Coated with Ag Material Prepared by Electroless Silver Plating

    NASA Astrophysics Data System (ADS)

    Huang, Bei; Gan, Weiping; Zhou, Jian; Li, Yingfen; Lin, Tao; Liu, Xiaogang

    2014-05-01

    Pb-based glass frit coated with nanosilver material for Si solar cell applications has been directly prepared by electroless silver plating. Activation of the glass frit was accomplished by using glycol, with the aim of reducing the silver ions to elemental silver on the surface of the glass frit. Electroless silver plating onto the glass frit was successfully realized using two kinds of electroless plating bath. However, the morphology of the composite powder greatly affected the modality, sheet resistance, series resistance, and photoelectric conversion efficiency of the conducting silver films. We found that the activation temperature affected the number and distribution of silver nanoparticles. Meanwhile, the average grain size of the silver particles and the silver content in the Pb-based glass frit coated with Ag material could be controlled by adjusting the pH value and loading capacity, respectively, during plating.

  5. Modifying the Surface of a Rashba-Split Pb-Ag Alloy Using Tailored Metal-Organic Bonds.

    PubMed

    Stadtmüller, Benjamin; Seidel, Johannes; Haag, Norman; Grad, Lisa; Tusche, Christian; van Straaten, Gerben; Franke, Markus; Kirschner, Jürgen; Kumpf, Christian; Cinchetti, Mirko; Aeschlimann, Martin

    2016-08-26

    Hybridization-related modifications of the first metal layer of a metal-organic interface are difficult to access experimentally and have been largely neglected so far. Here, we study the influence of specific chemical bonds (as formed by the organic molecules CuPc and PTCDA) on a Pb-Ag surface alloy. We find that delocalized van der Waals or weak chemical π-type bonds are not strong enough to alter the alloy, while localized σ-type bonds lead to a vertical displacement of the Pb surface atoms and to changes in the alloy's surface band structure. Our results provide an exciting platform for tuning the Rashba-type spin texture of surface alloys using organic molecules. PMID:27610875

  6. Modifying the Surface of a Rashba-Split Pb-Ag Alloy Using Tailored Metal-Organic Bonds.

    PubMed

    Stadtmüller, Benjamin; Seidel, Johannes; Haag, Norman; Grad, Lisa; Tusche, Christian; van Straaten, Gerben; Franke, Markus; Kirschner, Jürgen; Kumpf, Christian; Cinchetti, Mirko; Aeschlimann, Martin

    2016-08-26

    Hybridization-related modifications of the first metal layer of a metal-organic interface are difficult to access experimentally and have been largely neglected so far. Here, we study the influence of specific chemical bonds (as formed by the organic molecules CuPc and PTCDA) on a Pb-Ag surface alloy. We find that delocalized van der Waals or weak chemical π-type bonds are not strong enough to alter the alloy, while localized σ-type bonds lead to a vertical displacement of the Pb surface atoms and to changes in the alloy's surface band structure. Our results provide an exciting platform for tuning the Rashba-type spin texture of surface alloys using organic molecules.

  7. Effect of Ag-content on structure, corrosion behaviour and mechanical properties of Sn-9Zn lead-free solder alloy

    NASA Astrophysics Data System (ADS)

    Said Gouda, El; Abdel Aziz, H.; El Gendy, Y.; Saad Allah, F.; Hammam, M.

    2010-12-01

    The effect of (0.5-3.5) wt.% Ag additions on microstructure, melting, corrosion and mechanical properties of Sn-9Zn eutectic lead-free solder alloy has been studied and analyzed. The study included X-ray diffraction and scanning electron microscopy (SEM) to identify the microstructure of these alloys. The results showed that, continuous additions of Ag caused formation of Ag-Zn and Ag-Sn compounds which led to decrease the precipitations of Zn in Sn-matrix. These compounds led to increase the melting point of the alloys, which confirmed by the formation of small endothermic peaks in the higher temperature range followed the main peak of the DTA curves. Also, the DTA measurements confirmed that the alloy of composition Sn-9Zn-3.5Ag is the ternary eutectic alloy. Vicker's micro-hardness number of Sn-9Zn alloy increases with small additions of 0.5 and 1 wt.% Ag. Furthermore, it decreases to lower values with further increase of Ag content. Also, micro-creep behaviour, creep rate and corrosion behaviour of the Sn-9Zn-Ag alloys have been measured at room temperature.

  8. Microwave-assisted combustion synthesis of Ag/ZnO nanocomposites and their photocatalytic activities under ultraviolet and visible-light irradiation

    SciTech Connect

    Zhang, Dafeng; Pu, Xipeng; Li, Huaiyong; Yu, Young Moon; Shim, Jae Jeong; Cai, Peiqing; Kim, Sun Il; Seo, Hyo Jin

    2015-01-15

    Highlights: • Ag/ZnO nanocomposites were synthesized by a microwave-assisted combustion method. • Ag/ZnO nanocomposites exhibited improved photocatalytic activities under UV irradiation. • Poorer photocatalytic performances were obtained under visible-light irradiation. - Abstract: Ag/ZnO nanocomposites were synthesized by a rapid one-step microwave-assisted combustion method. The as-synthesized samples were characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, X-ray photoelectron spectroscopy, photoluminescence and ultraviolet–visible spectrophotometry. XRD results showed that hexagonal ZnO and cubic Ag were obtained. Ag nanoparticles were chemically attached on the surface of ZnO. The decrease in the energy band gap of Ag/ZnO nanocomposites and the photoluminescence quenching were observed while the Ag content was increased. Furthermore, the introduction of Ag nanoparticles leads to significantly improved photocatalytic activities in the case of ultraviolet irradiation, but in the case of visible-light irradiation opposite results were obtained. The corresponding mechanism was discussed in detail.

  9. Geology, isotope geochemistry and geochronology of the Jinshachang carbonate-hosted Pb-Zn deposit, southwest China

    NASA Astrophysics Data System (ADS)

    Zhou, Jia-Xi; Bai, Jun-Hao; Huang, Zhi-Long; Zhu, Dan; Yan, Zai-Fei; Lv, Zhi-Cheng

    2015-02-01

    The Jinshachang Pb-Zn deposit, an exceptionally radiogenic Pb-enriched sulfide deposit, hosted by dolostone of the Upper Sinian (Neoproterozoic) Dengying Formation and the Lower Cambrian Meishucun Formation, is located in the western Yangtze Block, about 300 km northeast of Kunming city in southwest China. Ore bodies in this deposit are dominated by strata-bound type and steeply dipping vein type. Primary ores in these two types are composed of sphalerite, galena, fluorite, barite and quartz with massive, banded, veined and disseminated structures. Twenty-seven ore bodies in the Jinshachang deposit host 4.6 million tons of sulfide ores at average grades of 4.07 wt.% Pb and 5.03 wt.% Zn. Quartz separates from the sulfide ores have δDH2O values ranging from -137‰ to -86.2‰ with an average of -114‰ (n = 7), lower than those of magmatic, metamorphic and meteoric water, suggesting a contribution of organic water. δ34SCDT values of ninety-one sulfide separates range from +1.1‰ to +13.4‰ with an average of +5.7‰, lower than those of evaporites (δ34SCDT = +15‰ to +35‰) in the Cambrian to Triassic sedimentary strata in NE Yunnan province. δ34SCDT values of eight barite separates range from +32‰ to +35‰ (average +34‰), within the range of evaporites. These data suggest that S2- in the hydrothermal fluids derived from evaporites by thermo-chemical sulfate reduction (TSR), whereas SO42- directly originated from the evaporites. Six sulfide separates have highly radiogenic 206Pb/204Pb ratios ranging from 20.74 to 21.18 (average 20.92), 207Pb/204Pb ratios ranging from 15.85 to 15.89 (average 15.87), and 208Pb/204Pb ratios ranging from 40.89 to 41.42 (average 41.16). The Pb isotopes of the sulfides plot above the upper crust Pb average evolution curve and overlap the Cambrian sedimentary rocks, but are different from the Sinian dolostone. This indicates a crustal source of Pb most likely derived from the Cambrian sedimentary rocks. The initial 87Sr/86Sr

  10. Effects of grinding and shaking on Cd, Pb and Zn distribution in anthropogenically impacted soils.

    PubMed

    Waterlot, Christophe; Bidar, Géraldine; Pruvot, Christelle; Douay, Francis

    2012-08-30

    The effects of grinding size and shaking process on the results of Cd (cadmium), Pb (lead) and Zn (zinc) distribution measurements three agricultural and three kitchen garden soils highly contaminated by past atmospheric fallout of two lead and zinc smelters in northern France were studied. The physico-chemical parameters and pseudo-total concentration of metals within these soils were determined. The fractionation of metals was performed in triplicate, using the procedure recommended by the Standards, Measurements and Testing program (SM&T), on each air-dried soil sample, ground to pass through 2-mm, 0.315-mm and 0.250-mm sieves and using a reciprocating or rotary shaker. The samples were analysed by flame or electrothermal absorption atomic spectrometry using a self-reversal background system. For both shaking processes, the grinding size had no effect on the fractionation of metals in contaminated agricultural soils. In contrast, using a reciprocating shaker, the fractionation of metals in the kitchen garden samples sieved at <2mm was so different that in the samples prepared to pass through the 0.315-mm and 0.250-mm sieves. Therefore changes (use of a 50 mL graduated polypropylene centrifuge tube, evaporation of the solution to a fixed volume in step 3 and the use of an automatic shaking heating bath) were made to the initial procedure and a rotary shaker was used to improve the suspension of the soil samples during extraction. For all grinding sizes, the fractionation of the three metals contained in the contaminated kitchen garden soil samples was successfully achieved. Nevertheless, some discrepancies from samples sieved at <2mm were obtained. On the other hand, it is worth noting that the effect of the type of shaker on the distribution of metal depended on the soil and the grinding size. From an analytical point of view, precision and trueness were improved after optimisation of the procedure for all sequential extraction procedure steps. The best results

  11. Effects of grinding and shaking on Cd, Pb and Zn distribution in anthropogenically impacted soils.

    PubMed

    Waterlot, Christophe; Bidar, Géraldine; Pruvot, Christelle; Douay, Francis

    2012-08-30

    The effects of grinding size and shaking process on the results of Cd (cadmium), Pb (lead) and Zn (zinc) distribution measurements three agricultural and three kitchen garden soils highly contaminated by past atmospheric fallout of two lead and zinc smelters in northern France were studied. The physico-chemical parameters and pseudo-total concentration of metals within these soils were determined. The fractionation of metals was performed in triplicate, using the procedure recommended by the Standards, Measurements and Testing program (SM&T), on each air-dried soil sample, ground to pass through 2-mm, 0.315-mm and 0.250-mm sieves and using a reciprocating or rotary shaker. The samples were analysed by flame or electrothermal absorption atomic spectrometry using a self-reversal background system. For both shaking processes, the grinding size had no effect on the fractionation of metals in contaminated agricultural soils. In contrast, using a reciprocating shaker, the fractionation of metals in the kitchen garden samples sieved at <2mm was so different that in the samples prepared to pass through the 0.315-mm and 0.250-mm sieves. Therefore changes (use of a 50 mL graduated polypropylene centrifuge tube, evaporation of the solution to a fixed volume in step 3 and the use of an automatic shaking heating bath) were made to the initial procedure and a rotary shaker was used to improve the suspension of the soil samples during extraction. For all grinding sizes, the fractionation of the three metals contained in the contaminated kitchen garden soil samples was successfully achieved. Nevertheless, some discrepancies from samples sieved at <2mm were obtained. On the other hand, it is worth noting that the effect of the type of shaker on the distribution of metal depended on the soil and the grinding size. From an analytical point of view, precision and trueness were improved after optimisation of the procedure for all sequential extraction procedure steps. The best results

  12. Facile synthesis of water-soluble Zn-doped AgIn5S8/ZnS core/shell fluorescent nanocrystals and their biological application.

    PubMed

    Song, Jiangluqi; Jiang, Tongtong; Guo, Tianyi; Liu, Ling; Wang, Huijie; Xia, Tongyan; Zhang, Wenting; Ye, Xuecheng; Yang, Mingya; Zhu, Lixin; Xia, Ruixiang; Xu, Xiaoliang

    2015-02-16

    Here we demonstrate a novel and facile strategy of highly luminescent water-soluble Zn-doped AgIn5S8 (ZAIS) nanocrystals and ZAIS/ZnS core/shell structures, which were based on hydrothermal reaction between the acetate salts of the corresponding metals and sulfide precursor in the presence of l-cysteine at 110 °C in a Teflon-lined autoclave. The photoluminescent (PL) emission wavelength can be conveniently tuned from 560 to 650 nm by tailoring the stoichiometric ratio of [Ag]/[Zn]. The as prepared nanocrystals were characterized systematically and exhibit long PL lifetimes more than 100 ns. The influence of experimental conditions, including concentration of l-cysteine and reaction temperature, was investigated. In addition, we performed a coating procedure with the ZnS shell outside the ZAIS core and showed excellent PL quantum yields up to 35%. The in vitro experiment exhibited quite low cytotoxicity and marvelous biocompatibility, revealing their promising prospect in bioscience. Furthermore, the obtained ZAIS/ZnS nanocompounds (NCs) were covalently conjugated to alpha-fetoprotein antibodies and targeted fluorescent imaging for hepatocellular carcinoma cells was realized. PMID:25594823

  13. The effects of biochars from rice residue on the formation of iron plaque and the accumulation of Cd, Zn, Pb, As in rice (Oryza sativa L.) seedlings.

    PubMed

    Zheng, Rui-Lun; Cai, Chao; Liang, Jian-Hong; Huang, Qing; Chen, Zheng; Huang, Yi-Zong; Arp, Hans Peter H; Sun, Guo-Xin

    2012-10-01

    A historically multi-metal contaminated soil was amended with biochars produced from different parts of rice plants (straw, husk and bran) to investigate how biochar can influence the mobility of Cd, Zn, Pb and As in rice seedlings (Oryza sativa L.). Rice shoot concentrations of Cd, Zn and Pb decreased by up to 98%, 83% and 72%, respectively, due to biochar amendment, though that of As increased by up to 327%. Biochar amendments significantly decreased pore water concentrations (C(pw)) of Cd and Zn and increased that of As. For Pb it depended on the amendment. Porewater pH, dissolved organic carbon, dissolved phosphorus, silicon in pore water and iron plaque formation on root surfaces all increased significantly after the amendments. The proportions of Cd and Pb in iron plaque increased by factors 1.8-5.7 and 1.4-2.8, respectively; no increase was observed for As and Zn. Straw-char application significantly and noticeably decreased the plant transfer coefficients of Cd and Pb. This study, the first to investigate changes in metal mobility and iron plaque formation in rice plants due to amending a historically contaminated soil with biochar, indicates that biochar has a potential to decrease Cd, Zn and Pb accumulations in rice shoot but increase that of As. The main cause is likely biochar decreasing the C(pw) of Cd and Zn, increasing the C(pw) of As, and increasing the iron plaque blocking capacity for Cd and Pb. PMID:22664390

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

    PubMed

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

    2009-10-15

    Lead pollution history over Northern Poland was reconstructed for the last ca. 1300 years using the elemental and Pb isotope geochemistry of a dated Polish peat bog. The data show that Polish Pb-Zn ores and coal were the main sources of Pb, other heavy metals and S over Northern Poland up until the industrial revolution. After review of the potential mobility of each element, most of the historical interpretation was based on Pb and Pb isotopes, the other chemical elements (Zn, Cu, Ni, S) being considered secondary indicators of pollution. During the last century, leaded gasoline also contributed to anthropogenic Pb pollution over Poland. Coal and Pb-Zn ores, however, remained important sources of pollution in Eastern European countries during the last 50 years, as demonstrated by a high (206)Pb/(207)Pb ratio (1.153) relative to that of Western Europe (ca. 1.10). The Pb data for the last century were also in good agreement with modelled Pb inventories over Poland and the Baltic region. PMID:19683332

  15. Precipitation in a Ag-Containing Mg-Y-Zn Alloy

    NASA Astrophysics Data System (ADS)

    Zhu, Y. M.; Oh-ishi, K.; Wilson, N. C.; Hono, K.; Morton, A. J.; Nie, J. F.

    2016-02-01

    The precipitation in a Mg-6Y-2Ag-1Zn-0.6Zr (wt pct) alloy during isothermal aging at and above 473 K (200 °C) has been examined systematically using conventional transmission electron microscopy, high-angle annular dark-field scanning transmission electron microscopy, and three-dimensional atom probe. The precipitation involves the formation of G.P. zones, metastable γ″ and γ' phases, and equilibrium 14H and δ phases. The G.P. zones are a single atomic layer on (0001) α . The γ″ is the key strengthening phase and it has an ordered hexagonal structure ( P6/mmm, a = 0.556 nm, c = 0.424 nm). The γ″ forms as (0001) α plates with a thickness of a single unit cell height and tends to develop into stacks with irregular spacing when the alloy is exposed to longer aging time at 473 K (200 °C). The γ″ is gradually replaced by γ' and 14H during prolonged aging at 473 K (200 °C) and/or temperatures above 473 K (200 °C). The equilibrium δ phase is also found in grain boundaries. The results are compared with findings in other but similar alloy systems, and approaches for enhancing γ″ nucleation rate and hence further improvement in alloy age-hardening response are discussed. The effects of Ag on precipitation are also discussed.

  16. Photocatalytic activity of ZnO doped with Ag on the degradation of endocrine disrupting under UV irradiation and the investigation of its antibacterial activity

    NASA Astrophysics Data System (ADS)

    Bechambi, Olfa; Chalbi, Manel; Najjar, Wahiba; Sayadi, Sami

    2015-08-01

    Ag-doped ZnO photocatalysts with different Ag molar content (0.0, 0.5, 1.0, 2.0 and 4.0%) were prepared via hydrothermal method. The X-ray diffraction (XRD), Nitrogen physisorption at 77 K, Fourier transformed infrared spectroscopy (FTIR), UV--Visible spectroscopy, Photoluminescence spectra (PL) and Raman spectroscopy were used to characterize the structural, textural and optical properties of the samples. The results showed that Ag-doping does not change the average crystallite size with the Ag low content (≤1.0%) but slightly decreases with Ag high content (>1.0%). The specific surface area (SBET) increases with the increase of the Ag content. The band gap values of ZnO are decreased with the increase of the Ag doping level. The results of the photocatalytic degradation of bisphenol A (BPA) and nonylphenol (NP) in aqueous solutions under UV irradiation and in the presence of hydrogen peroxide (H2O2) showed that silver ions doping greatly improved the photocatalytic efficiency of ZnO. The TOC conversion BPA and NP are 72.1% and 81.08% respectively obtained using 1% Ag-doped ZnO. The enhancement of photocatalytic activity is ascribed to the fact that the modification of ZnO with an appropriate amount of Ag can increase the separation efficiency of the photogenerated electrons-holes in ZnO. The antibacterial activity of the catalysts which uses Escherichia coli as a model for Gram-negative bacteria confirmed that Ag-doped ZnO possessed more antibacterial activity than the pure ZnO.

  17. Orientation dependence of electrocaloric effects in Pb(Zn1/3Nb2/3)-PbTiO3 single crystals

    NASA Astrophysics Data System (ADS)

    Chukka, Rami; Vandrangi, Suresh; Chen, Zuhuang; You, Lu; Wang, Junling; Yang, Ping; Chen, Lang

    2013-07-01

    Electrocaloric effects of (001), (011) and (111) oriented single crystals have been thoroughly investigated to study the ferroelectric-ferroelectric (FE-FE) phase transition induced isothermal entropy changes in 0.94Pb(Zn1/3Nb2/3)O3-0.06PbTiO3 (PZN-PT) material. The results showed that the PZN-PT crystals oriented in (111) direction exhibit ˜ 38% higher electrocaloric cooling values near lower critical phase transitions from rhombohedral (R) to tetragonal (T) phases in PZN-PT crystals, compared to those oriented in (011) direction. Though (111) samples display higher cooling values, (011) samples showed broader cooling curves due to their easily switchable characteristics between R and T phases.

  18. Mass spectrometry and potentiometry studies of Pb(II)-, Cd(II)- and Zn(II)-cystine complexes.

    PubMed

    Furia, Emilia; Aiello, Donatella; Di Donna, Leonardo; Mazzotti, Fabio; Tagarelli, Antonio; Thangavel, Hariprasad; Napoli, Anna; Sindona, Giovanni

    2014-01-21

    Cd(II)-, Pb(II)- and Zn(II)-cystine complexes were investigated by potentiometric and different mass spectrometric (MS) methodologies. Laser desorption mass spectrometry has provided both the composition and structure of metal-cystine complexes according to the speciation models proposed on the basis of the potentiometric data. Detection of neutral complexes was achieved by protonation or electrochemical reduction during mass spectrometric experiments. The redox activity of metal-cystine complexes was confirmed by laser desorption and charge transfer matrix assisted laser assisted MS experiments, which allowed us to observe the formation of complexes with a reduction of cystine. The stoichiometry of Cd(II)-, Pb(II)- and Zn(II)-cystine complexes was defined by observing the isotopic pattern of the investigated compound. The results suggest that interaction occurs through the carboxylate group of the ligand.

  19. [Effects of fly ash on the exchangeable heavy metals (Cu, Zn, Pb) during sewage sludge composting and land utilization].

    PubMed

    Sheng, Jun; Lu, Wen-Jing; Wang, Hong-Tao

    2007-06-01

    A series of composting test using fly ash as stabilizing agent were investigated to study the variation of the exchangeable heavy metals during composting and land utilization. A whole procedure of adsorption and desorption of stabilized heavy metals were analyzed. The result shows that the exchangeable Cu increases while the exchangeable Zn and Pb decrease during composting. Fly ash has significant stabilizing effect on Zn and Pb as evidenced by a decline of 62.47% and 92.61% respectively in the trails with flay ash as stabilizing agent. However there is no obvious change with exchangeable Cu. Although there is a big difference on the activities of heavy metals in different soil types tested, it seems to be ineluctable that addition of sewage sludge composting products cause enrichment of heavy metal in soil.

  20. Colonisation of a Zn, Cd and Pb hyperaccumulator Thlaspi praecox Wulfen with indigenous arbuscular mycorrhizal fungal mixture induces changes in heavy metal and nutrient uptake.

    PubMed

    Vogel-Mikus, Katarina; Pongrac, Paula; Kump, Peter; Necemer, Marijan; Regvar, Marjana

    2006-01-01

    Plants of the Zn, Cd and Pb hyperaccumulator Thlaspi praecox Wulfen (Brassicaceae) inoculated or not with indigenous arbuscular mycorrhizal (AM) fungal mixture were grown in a highly Cd, Zn and Pb contaminated substrate in order to evaluate the functionality of symbiosis and assess the possible impact of AM colonisation on heavy metal uptake and tolerance. The results suggest AM development in the metal hyperaccumulating T. praecox is favoured at elevated nutrient demands, e.g. during the reproductive period. AM colonisation parameters positively correlated with total soil Cd and Pb. Colonised plants showed significantly improved nutrient and a decreased Cd and Zn uptake as revealed by TRXRF, thus confirming the functionality of the symbiosis. Reduced heavy metal uptake, especially at higher soil metal contents, indicates a changed metal tolerance strategy in colonised T. praecox plants. This is to our knowledge the first report on AM colonisation of the Zn, Cd and Pb hyperaccumulator T. praecox in a greenhouse experiment. PMID:15998561

  1. Direct determination of Cu, Mn, Pb, and Zn in beer by thermospray flame furnace atomic absorption spectrometry

    NASA Astrophysics Data System (ADS)

    Nascentes, Clésia C.; Kamogawa, Marcos Y.; Fernandes, Kelly G.; Arruda, Marco A. Z.; Nogueira, Ana Rita A.; Nóbrega, Joaquim A.

    2005-06-01

    In this work, thermospray flame furnace atomic absorption spectrometry (TS-FF-AAS) was employed for Cu, Mn, Pb, and Zn determination in beer without any sample digestion. The system was optimized and calibration was based on the analyte addition technique. A sample volume of 300 μl was introduced into the hot Ni tube at a flow-rate of 0.4 ml min -1 using 0.14 mol l -1 nitric acid solution or air as carrier. Different Brazilian beers were directly analyzed after ultrasonic degasification. Results were compared with those obtained by graphite furnace atomic absorption spectrometry (GFAAS). The detection limits obtained for Cu, Mn, Pb, and Zn in aqueous solution were 2.2, 18, 1.6, and 0.9 μg l -1, respectively. The relative standard deviations varied from 2.7% to 7.3% ( n=8) for solutions containing the analytes in the 25-50 μg l -1 range. The concentration ranges obtained for analytes in beer samples were: Cu: 38.0-155 μg l -1; Mn: 110-348 μg l -1, Pb: 13.0-32.9 μg l -1, and Zn: 52.7-226 μg l -1. Results obtained by TS-FF-AAS and GFAAS were in agreement at a 95% confidence level. The proposed method is fast and simple, since sample digestion is not required and sensitivity can be improved without using expensive devices. The TS-FF-AAS presented suitable sensitivity for determination of Cu, Mn, Pb, and Zn in the quality control of a brewery.

  2. Proterozoic Carbonate Lithofacies Control the Distribution of Sulphides at the Gayna River Zn-Pb Camp, Mackenzie Mountains, NWT

    NASA Astrophysics Data System (ADS)

    Turner, E. C.

    2009-05-01

    Zn-Pb deposits at Gayna River, NWT are predominantly concentrated in the informal 'Grainstone formation', a dolostone of the early Neoproterozoic Little Dal Group (Mackenzie Mountains Supergroup). Previous work showed that the mineralisation (inferred 50 Mt combined from numerous zones; 5 percent combined Zn+Pb) is fracture-controlled and spatially associated with giant stromatolite reefs (500 m thick) of the underlying formation. The rheologically brittle, uncompactable and hydrologically tight reef masses are enclosed by coeval, compacted shale and deep-water limestone. A long and complex history of reef growth controlled by sea-level change resulted in a distinctive reef morphology that includes a sharp right-angle at all reef-top margins, where heterogeneous, off-reef limestone, shale and dolostone abut the rigid, lithologically homogeneous reefs. These zones of abrupt lateral facies change, between uncompactable reef and ductile, layered off-reef strata, represent the structurally weakest points in the system, where, during even subtle later tectonic events, stress would be preferentially accommodated. Brittle deformation of competent carbonate layers in this inflection zone in response to stress produced fracture haloes around reef-tops, which were then occluded by Zn-Pb sulphides. Abrupt competence contrasts appear to be necessary for the production of fractures that control the locations of sulphides at Gayna River. The dominant fractures in the Gayna River camp are those associated with reef- tops. The plan shape and location of buried reef-tops are probably the most critical controls on the distribution of hitherto undiscovered sulphide masses in the subsurface. Careful mapping of those depositional lithofacies that are characteristic of near-reef environments and of subtle, compaction-related dips in appropriate stratigraphic levels may provide vectors to as-yet unrecognised subsurface reef-margin zones favourable for Zn-Pb mineralisation. Structures and

  3. Kinetic rate laws of Cd, Pb, and Zn vaporization during municipal solid waste incineration.

    PubMed

    Falcoz, Quentin; Gauthier, Daniel; Abanades, Stéphane; Flamant, Gilles; Patisson, Fabrice

    2009-03-15

    The kinetic rate laws of heavy metal (HM) vaporization from municipal solid waste during its incineration were studied. Realistic artificial waste (RAW) samples spiked with Pb, Zn, and Cd were injected into a fluidized bed reactor. Metal vaporization wastracked by continuous measure ofthe above metals in exhaust gases. An inverse model of the reactor was used to calculate the metal vaporization rates from the concentration vs time profiles in the outlet gas. For each metal, experiments were carried out at several temperatures in order to determine the kinetic parameters and to obtain specific rate laws as functions of temperature. Temperature has a strong influence on the HM vaporization dynamics, especially on the vaporization kinetics profile. This phenomenon was attributed to internal diffusion control of the HM release. Two types of kinetic rate laws were established based on temperature: a fourth- or fifth-order polynomial rate law (r(x) = k0e(-E(A)/RT)p(x)) for temperatures lower than 740 degrees C and a first-order polynomial (r(x) = k0e(-E(A)/ RT(q-q(f) for temperatures higher than 740 degrees C.

  4. ZnO/PbTiO3 as a Novel Catalyst for CO2 Conversion

    NASA Astrophysics Data System (ADS)

    Alawode, Babatunde; Kolpak, Alexie

    2014-03-01

    Due to its role in climate change, there is a great interest in finding ways to take advantage of the vast amount of waste CO2 we produce by its conversion to useful substances. This is currently impractical due to the high temperatures and pressures generally required for the synthesis of compounds using CO2 as a precursor. To make direct CO2 capture and conversion economically viable, new materials able to catalyze the conversion reactions at significantly milder conditions will be essential. In this work, we use DFT computations to design a dynamically tunable ferroelectric oxide-supported thin film catalyst that can capture CO2 directly from the emission stream and convert it into methanol or cyclic carbonates. One promising candidate for a dynamically tunable catalyst of this type is ZnxOy/PbTiO3. We demonstrate that switching the polarization of the ferroelectric substrate substantially changes the surface atomic and electronic properties of the heterostructure, thereby enabling tunable absorption. We investigate reaction pathways on unsupported and supported ZnO for common CO2 reactions. Our approach may lead not only to new technologies for reducing emissions, but also to novel catalysts that could decrease energy consumption for industrial-scale synthetic processes.

  5. Effect of combined microbes on plant tolerance to Zn-Pb contaminations.

    PubMed

    Ogar, Anna; Sobczyk, Łukasz; Turnau, Katarzyna

    2015-12-01

    The presence and composition of soil microbial communities has been shown to have a large impact on plant-plant interactions and consequently plant diversity and composition. The goal of the present study was to evaluate impact of arbuscular mycorrhizal fungi (AMF) and nitrogen-fixing bacteria, which constitutes an essential link between the soil and the plant's roots. A greenhouse pot experiment was conducted to evaluate the feasibility of using selected microbes to improve Hieracium pilosella and Medicago sativa growth on Zn-Pb-rich site. Results of studies revealed that biomass, the dry mass of shoots and roots, increased significantly when plants were inoculated with mycorrhizal fungi and nitrogen-fixing bacteria. The addition of Azospirillum sp. and Nostoc edaphicum without mycorrhiza suppressed plant growth. Single bacterial inoculation alone does not have a positive effect on M. sativa growth, while co-inoculation with AMF improved plant growth. Plant vitality (expressed by the performance index) was improved by the addition of microbes. However, our results indicated that even dry heat sterilization of the substratum created imbalanced relationships between soil-plant and plants and associated microorganisms. The studies indicated that AMF and N2-fixers can improve revegetation of heavy metal-rich industrial sites, if the selection of interacting symbionts is properly conducted. PMID:26250813

  6. Effects of heavy metals (Cd, Cu, Cr, Pb, Zn) on fish glutathione metabolism.

    PubMed

    Eroglu, A; Dogan, Z; Kanak, E G; Atli, G; Canli, M

    2015-03-01

    The glutathione metabolism contains crucial antioxidant molecules to defend the organisms against oxidants. Thus, the aim of this study was to investigate the response of the glutathione metabolism in the liver of freshwater fish Oreochromis niloticus exposed to metals (Cu, Cd, Cr, Pb, Zn) in different periods. Fish were exposed to metals (as 1 μg/mL) individually for 1, 7, and 14 days and subsequently antioxidant enzymes (glutathione peroxidase, GPX; glutathione reductase, GR and glutathione S-transferase, GST) and glutathione levels (total glutathione, tGSH; reduced glutathione, rGSH; oxidized glutathione, GSSG and GSH/GSSG ratios) in the liver were measured. There was no fish mortality during the experiments, except Cu exposure. The antioxidant enzymes responded differently to metal exposures depending on metal types and exposure durations. GPX activity increased only after Cd exposure, while GST activity increased following 7 days of all metal exposures. However, GR activity did not alter in most cases. Total GSH and GSH/GSSG levels generally decreased, especially after 7 days. Data showed that metal exposures significantly altered the response of antioxidant system parameters, particularly at day 7 and some recovery occurred after 14 days. This study suggests that the response of antioxidant system could help to predict metal toxicity in the aquatic environments and be useful as an "early warning tool" in natural monitoring studies.

  7. Structure, hydrothermal alteration and composition of the Rubiales Pb-Zn orebody (Lugo, Spain): Genetic model

    NASA Astrophysics Data System (ADS)

    Arias, D.; Suárez, O.; Corretgé, L. G.; Fernández-Jardón, L.; Pérez-Cerdán, F.

    1991-07-01

    The Rubiales Pb-Zn ore deposit, northwestern Spain, is situated in the Westasturian-Leonese zone, according to the division of the Hercynian Chain in the Iberian Peninsula (Julivert et al. 1972). The orebody is placed in a subvertical shear zone developed at the eastern limb of the Baralla syncline, within the middle and upper members of the lower Cambrian Transition Series. The deposit is a vertical lenticular mass with a N30°W direction. Its length is about 1200 m in a N-S direction by 600 m wide and has an average thickness of 30 m. Its mineralogy is simple: 99% of the sulphides consist of sphalerite and galena with a ratio of 7 to 1. The remaining 1% is mainly formed by pyrite and chalcopyrite with pyrrhotite traces. The deposit shows a large aureole of hydrothermal alteration which is the result of three consecutive processes: (1) sericitization of slates and ankeritization of limestones; (2) silicification of ankeritic rocks; and (3) chloritization of the lower part of the deposit. Since the deposit was discovered in 1967 there has been controversy concerning its origin. Two hypotheses have been considered so far: (1) a sedex model formation (Gilissen 1977; Vazquez 1987); and (2) a hydrothermal origin in a shear zone during the Hercynian Orogeny (Merayo et al. 1984; Arias 1988). The data herein presented support the second hypothesis.

  8. Penta­lanthanum zinc diplumbide, La5Zn1−xPb2+x (x ≃ 0.6)

    PubMed Central

    Oshchapovsky, Igor; Pavlyuk, Volodymyr; Dmytriv, Grygoriy; Harbrecht, Bernd

    2014-01-01

    The title non-stoichiometric penta­lanthanum zinc diplumbide, La5Zn1−xPb2+x (x ≃ 0.6), was prepared from the elements in an evacuated silica ampoule. It adopts the Nb5Sn2Si-type structure (space group I4/mcm, Pearson symbol tI32), a ternary ordered superstructure of the W5Si3 type. Among the four independent crystallographic positions, three are fully occupied by La (Wyckoff 16k), La (4b), and Pb (8h) and one is occupied by a statistical mixture [occupancy ratio 0.394 (12):0.606 (12)] of Zn and Pb (4a). The structure is constructed by face-sharing 10-vertex polyhedra around the unmixed Pb sites. These fragments enclose channels of trans-face-sharing tetra­gonal anti­prisms occupied by the disordered Zn and Pb sites. PMID:24526938

  9. [Effects of Remedies on the Remediation of Typical Pb and Zn-contaminated soil in Huanjiang, Guangxi].

    PubMed

    Zeng, Wei-quan; Song, Bo; Yuan, Li-zhu; Huang, Yu-fei; Fu, Feng-yan

    2015-06-01

    Due to the collapse of the Pb/Zn tailing dam of Huanjiang, Guangxi, the farmland along Huanjiang River are strongly acidic and heavy metal-contaminated, resulting in the loss of agricultural production. To explore some remedies and the migration of heavy metals in heavy metal contaminated-soil of Huanjiang, this study investigated the effects of different types of amendments (lime, calcium magnesium phosphate, organic fertilizer, polypropylene amide) on tested soils through soil leaching test. The results showed that T1 soil was severely acidified, reducing the pH of the soil layer to clean contact, while T2, T3, T4, T5 could significantly improve the contaminated soil pH, ranging from 2.7 to 3.2, 1.6 to 2.7 respectively. Compared with T1, in the contaminated soil at 0-20 cm, T2, T3, T4, T5 could effectively activate Pb and immobilize Zn. Compared with T1, in 20-60 cm clean soil, there was no significant differences in the effect of different treatments on DTPA-Pb and DTPA-Zn (P < 0.05). Compared with T1, T4 and T5 could provide good growing conditions for plants, which might provide technical support for future measurements such as bioremediation. PMID:26387340

  10. Use of bone meal amendments to immobilise Pb, Zn and Cd in soil: A leaching column study.

    PubMed

    Sneddon, I R; Orueetxebarria, M; Hodson, M E; Schofield, P F; Valsami-Jones, E

    2006-12-01

    The aim of this study is to test the stabilisation of metals in contaminated soils via the formation of low-solubility metal phosphates. Bone apatite, in the form of commercially available bone meal, was tested as a phosphate source on a mine waste contaminated made-ground with high levels of Pb, Zn and Cd. Triplicate leaching columns were set up at bone meal to soil ratios of 1:25 and 1:10, in addition to unamended controls, and were run for 18 months. The columns were irrigated daily with a synthetic rain solution at pH of 2, 3, and 4.4. After 100 days, the leachate Pb, Zn and Cd concentrations of all amended columns were significantly reduced. For 1:10 treatments, release of these metals was suppressed throughout the trial. For 1:25 treatments, Zn and Cd concentrations in the leachates began to increase after 300 days. DTPA and water extractions showed that Pb and Cd were more strongly held in the amended soils. This study concludes that the complexity of soil processes and the small quantities of metals sequestered precluded determination of a metal immobilisation mechanism.

  11. Characterization of cadmium biosorption by Exiguobacterium sp. isolated from farmland soil near Cu-Pb-Zn mine.

    PubMed

    Park, Jin Hee; Chon, Hyo-Taek

    2016-06-01

    Bacteria have the ability to bind heavy metals on their cell wall. Biosorption is a passive and energy-independent mechanism to adsorb heavy metals. The efficiency of heavy metal biosorption can vary depending on several factors such as the growth phase of bacteria, solution pH, and existence of competitive heavy metals. In this study, Exiguobacterium sp. isolated from farmland soil near a mine site were used, and optimal conditions for Cd biosorption in solution were investigated. As bacterial growth progressed, Cd biosorption increased, which is attributed to changes in the structure and composition of the cell wall during bacterial growth. The biosorption process was rapid and was completed within 30 min. Cadmium biosorption was highest at pH 7 due to the dissociation of hydrogen ions and the increase of negative charges with increasing pH. In the mixed metal solution of Cd, Pb, and Zn, the amount of biosorption was in the order of Pb>Cd>Zn while in a single metal solution, the order was Cd≥Pb>Zn. The maximum adsorption capacity for Cd by the isolated bacteria was 15.6 mg/g biomass, which was calculated from the Langmuir isotherm model. Different adsorption efficiencies under various environmental conditions indicate that, to control metal mobility, the conditions for biosorption should be optimized before applying bacteria. The results showed that the isolated bacteria can be used to immobilize metals in metal-contaminated wastewater.

  12. Influences of traffic on Pb, Cu and Zn concentrations in roadside soils of an urban park in Dublin, Ireland.

    PubMed

    Dao, Ligang; Morrison, Liam; Zhang, Hongxuan; Zhang, Chaosheng

    2014-06-01

    Soils in the vicinity of roads are recipients of contaminants from traffic emissions. In order to obtain a better understanding of the impacts of traffic on soils, a total of 225 surface soil samples were collected from an urban park (Phoenix Park, Dublin, Ireland) in a grid system. Metal (Pb, Cu and Zn) concentrations were determined using a portable X-ray fluorescence analyzer. Strong spatial variations for the concentrations of Pb, Cu and Zn were observed. The spatial distribution maps created using geographical information system techniques revealed elevated metal concentrations close to the main traffic route in the park. The relationships between the accumulation of Pb, Cu and Zn in the roadside soils and the distance from the road were well fitted with an exponential model. Elevated metal concentrations from traffic pollution extended to a distance of approximately 40 m from the roadside. The results of this study provide useful information for the management of urban parks particularly in relation to policies aimed at reducing the impact of traffic related pollution on soils.

  13. Characterization of cadmium biosorption by Exiguobacterium sp. isolated from farmland soil near Cu-Pb-Zn mine.

    PubMed

    Park, Jin Hee; Chon, Hyo-Taek

    2016-06-01

    Bacteria have the ability to bind heavy metals on their cell wall. Biosorption is a passive and energy-independent mechanism to adsorb heavy metals. The efficiency of heavy metal biosorption can vary depending on several factors such as the growth phase of bacteria, solution pH, and existence of competitive heavy metals. In this study, Exiguobacterium sp. isolated from farmland soil near a mine site were used, and optimal conditions for Cd biosorption in solution were investigated. As bacterial growth progressed, Cd biosorption increased, which is attributed to changes in the structure and composition of the cell wall during bacterial growth. The biosorption process was rapid and was completed within 30 min. Cadmium biosorption was highest at pH 7 due to the dissociation of hydrogen ions and the increase of negative charges with increasing pH. In the mixed metal solution of Cd, Pb, and Zn, the amount of biosorption was in the order of Pb>Cd>Zn while in a single metal solution, the order was Cd≥Pb>Zn. The maximum adsorption capacity for Cd by the isolated bacteria was 15.6 mg/g biomass, which was calculated from the Langmuir isotherm model. Different adsorption efficiencies under various environmental conditions indicate that, to control metal mobility, the conditions for biosorption should be optimized before applying bacteria. The results showed that the isolated bacteria can be used to immobilize metals in metal-contaminated wastewater. PMID:26951224

  14. Use of microbial community to evaluate performance of a wetland system in treating Pb/Zn mine drainage.

    PubMed

    Yu, Yu H; Feng, Wei S; Shen, Yun F; Ye, Zhi H; Wong, Ming H

    2005-12-01

    The performance of a wetland system in treating lead (Pb)/zinc (Zn) mine drainage was evaluated by using the polyurethane foam unit (PFU) microbial community (method), which has been adopted by China as a standardized procedure for monitoring water quality. The wetland system consisted of four cells with three dominant plants: Typha latifolia, Phragmites australis and Paspalum distichum. Physicochemical characteristics [pH, EC, content of total suspended solid (TSS) and metals (Pb, Zn, Cd, and Cu)] and PFU microbial community in water samples had been investigated from seven sampling sites. The results indicated that the concentrations of Pb, Zn, Cd, Cu, and TSS in the mine drainage were gradually reduced from the inlet to the outlet of the wetland system and 99%, 98%, 75%, 83%, and 68% of these metals and TSS respectively, had been reduced in concentration after the drainage passed through the wetland system. A total of 105 protozoan species were identified, the number of protozoa species and the diversity index (DI) gradually increased, while the heterotrophic index (HI) gradually decreased from the inlet to the outlet of the wetland system. The results indicated that DI, HI, and total number species of protozoa could be used as biological indicators indicating the improvement of water quality.

  15. A comparative study of the most effective amendment for Pb, Zn and Cd immobilization in contaminated soils.

    PubMed

    Szrek, Dominik; Bajda, Tomasz; Manecki, Maciej

    2011-01-01

    The problem of an extensive contamination of soils with metals can be resolved using an in situ chemical immobilization technology. Five substances (natural zeolite, bog iron ore, "Polifoska 15" fertilizer, triple superphosphate, diammonium phosphate) were tested to determine their efficiency to immobilize Zn, Pb and Cd in smelter-contaminated soil in the Upper Silesia region. Soil samples were collected at three sites located in the vincity of a Pb-Zn smelter and a sludge landfill near the town of Bukowno. Effective reduction of leachable and fitoavailable Zn, Pb and Cd concentrations in soil was observed after addition of diammonium phosphate, "Polifoska 15" fertilizer and bog iron ore amendments. Additional test proved that immobilization effect gained by these amendments sustains at low-temperature conditions. It was noticed that phosphate addition resulted in lowering pH and mobilization of As(V) in soils. Good immobilization effectiveness and lack of major adverse effects of bog iron application suggest that this is the method of choice. PMID:21961559

  16. Geochemical partitioning of Pb, Zn, Cu, Fe, and Mn across the sediment-water interface in large lakes

    SciTech Connect

    McKee, J.D.; Wilson, T.P.; Long, D.T.; Owen, R.M.

    1989-01-01

    The early diagenetic remobilization of Mn, Fe, Zn, Cu, and Pb was evaluated by studying the geochemical partitioning of the metals among hydromorphic phases in interfacial sediment and in the sediment column, at a site in the Caribou sub-basin, Lake Superior. The sediment was collected with a vacuum/filtration system developed for the submersible Johnson Sea-Link II and the sediment column by gravity coring. The results show that: (1) Pb, Cu, and Zn exhibit sediment profiles in which their concentrations decrease with depth for total metal and some of the hydromorphic phases; (2) Mn and Fe profiles are the result of early diagenesis; (3) each of the metals is uniquely partitioned among the phases and the partitioning changes from the sediment to the sediment column and with depth; and (4) the concentrations of Zn, Cu, and Pb in the sediment are higher than those in the sediment column and, in some instances, appear to be an exponential extrapolations of the latter. The results are interpreted to indicate that the metals are remobilized during early diagenesis and that the sediment may be chemically unique compared to the sediment column, perhaps being similar to interfacial sediments identified in deep marine environments. In addition, it appears that studying the metal concentrations in the individual hydromorphic phases of the sediment is more useful in identifying diagenetic processes than is examination of either total hydromorphic or total metal concentrations of the sediment.

  17. Interplay Between Expression of Sulfur Assimilation Pathway Genes and Zn(2+) and Pb(2+) Stress in Acidithiobacillus ferrooxidans.

    PubMed

    Zheng, Chunli; Chen, Minjie; Wang, Dan; Zhang, Li; Wang, JianYing; Zhang, Xuefeng

    2016-10-01

    We have previously demonstrated that in Acidithiobacillus ferrooxidans, resistance to the highly toxic divalent cation Cd(2+) is mediated in part by the sulfur assimilation pathway (SAP) and enhanced intracellular concentrations of cysteine and glutathione(GSH) (Zheng et al., Extremophiles 19:429-436, 2015). In this paper, we investigate the interplay between Zn(2+) and Pb(2+) resistances, SAP gene expression, and thiol-containing metabolite levels. Cells grown in the presence of 300 mM Zn(2+) had enhanced activities of the following enzymes: adenosylphosphosulphate reductase (APR, 40-fold), serine acetyltransferase (SAT, 180-fold), and O-acetylserine (thiol) lyase (OAS-TL, 230-fold). We investigated the concentrations of mRNA transcripts of the genes encoding these enzymes in cells grown in the presence of 600 mM Zn(2+): transcripts for 4 SAP genes-ATPS(ATP sulphurylase), APR, SiR(sulfite reductase), SAT, and OAS-TL-each showed a more than three-fold increase in concentration. At the metabolite level, concentrations of intracellular cysteine and glutathione (GSH) were nearly doubled. When cells were grown in the presence of 10 mM Pb(2+), SAP gene transcript concentrations, cysteine, and GSH concentrations were all decreased, as were SAP enzyme activities. These results suggested that Zn(2+) induced SAP pathway gene transcription, while Pb(2+) inhibited SAP gene expression and enzyme activities compared to the pathway in most organisms. Because of the detoxification function of thiol pool, the results also suggested that the high resistance of A. ferrooxidans to Zn(2+) may also be due to regulation of GSH and the cysteine synthesis pathway. PMID:27376536

  18. Multi-metal interactions between Cd, Cu, Ni, Pb and Zn in water flea Daphnia magna, a stable isotope experiment.

    PubMed

    Komjarova, I; Blust, R

    2008-11-11

    Metal interaction effects were investigated in Daphnia magna during a simultaneous exposure to essential (Cu, Ni and Zn) and non-essential (Cd and Pb) metals at environmentally relevant concentrations using a stable isotope technique. The metals were applied in the following concentration ranges: 0.0125-0.2 microM for (106)Cd, 0.025-0.25 microM for (65)Cu and (204)Pb, 0.1-1.25 microM for (62)Ni and (67)Zn. Cadmium and copper exhibited a suppressing effect on the uptake rates of all other metals present in the mixture with the exception to lead at all studied concentrations. The effect was already pronounced at low Cd and Cu concentrations and reached a maximum at the higher concentrations. Nickel and zinc showed weaker interactions with cadmium and between each other, while having no effect on copper and lead uptake. There was a high degree of correlation between Cd, Ni and Zn uptake rates indicating that these metals share in part common uptake or interaction pathways. Moreover, a significant correlation between Zn and Cu uptake processes suggests that more than one mechanism is involved in Zn accumulation since Cu is known to interact with Na uptake sites. The uptake of lead was marked by a high initial rate, but the uptake process reached saturation within 24 h. Cd applied at a concentration of 0.2 microM was the only metal which affected the lead uptake process by stimulation of the Pb uptake. Added to the medium at a concentration of 0.25 microM, lead in turn, increased copper uptake. Current work illustrates that metal interactions are significant and occur at low environmentally realistic concentrations affecting bioavailability of both toxic and essential metals.

  19. The effect of Zn, Ag and Au substitution for Cu in Finemet on the crystallization and magnetic properties

    NASA Astrophysics Data System (ADS)

    Chau, N.; Hoa, N. Q.; The, N. D.; Vu, L. V.

    2006-08-01

    Soft magnetic ribbons of Finemet compound with Zn, Ag and Au substituted for Cu: Fe 73.5Si 13.5B 9Nb 3Cu 1-xM x (M=Zn, Ag, Au; x=0.5, 1.0) have been fabricated by rapid quenching technique with wheel speeds of 10, 25 and 30 m/s, respectively. The crystallization evolution of samples examined by DSC measurements showed that the high cooling rates make the ribbons in amorphous state whereas the samples with M=Zn; x=0.5, 1.0 showed to be partly crystallized when they fabricated by the wheel speed of 10 m/s. In the case of Zn ( x=0.5, 1.0) and Ag ( x=1.0) substitution there is a sharp peak in the DSC curve corresponding to crystallization of α-Fe(Si) phase. However, the role of Au is similar to that of Cu. Hysteresis loops of as-cast samples exhibited square form which relates to the pinning centers in domain wall displacement. After appropriate annealing, the ultrasoft magnetic properties of studied ribbons are obtained.

  20. Anomalous temperature-dependent Young's modulus of a cast LAST (Pb-Sb-Ag-Te) thermoelectric material

    SciTech Connect

    Ren, Fei; Case, Eldon D; Timm, Edward J; Lara-Curzio, Edgar; Trejo, Rosa M

    2010-01-01

    Thermomechanical characterization is important to material evaluation and device design in the development of thermoelectric technology. In this study, we utilize the resonant ultrasound spectroscopy (RUS) technique to examine the elastic behavior of a cast LAST (Pb Sb Ag Te) material with a composition of Ag0.86Pb19Sb1.0Te20 between room temperature and 823 K. The temperature-dependent Young s modulus exhibits a monotonically decreasing trend with increasing temperature. However, an abnormal slope change in the Young s modulus temperature curve around 500 K is observed. In addition, hysteresis between heating and cooling data in the temperature range of 450 550 K is observed, which appears to be dependent on the heating/cooling rate during the RUS experiments such that the hysteresis disappears when the heating/cooling rate was decreased from 5 to 2 K min 1. In this study we propose an order disorder transition model for the anomalous temperature-dependent Young s modulus behavior observed in this study.

  1. Impact of multi-metals (Cd, Pb and Zn) exposure on the physiology of the yeast Pichia kudriavzevii.

    PubMed

    Mesquita, Vanessa A; Machado, Manuela D; Silva, Cristina F; Soares, Eduardo V

    2015-07-01

    Metal contamination of the environment is frequently associated to the presence of two or more metals. This work aimed to study the impact of a mixture of metals (Cd, Pb and Zn) on the physiology of the non-conventional yeast Pichia kudriavzevii. The incubation of yeast cells with 5 mg/l Cd, 10 mg/l Pb and 5 mg/l Zn, for 6 h, induced a loss of metabolic activity (assessed by FUN-1 staining) and proliferation capacity (evaluated by a clonogenic assay), with a small loss of membrane integrity (measured by trypan blue exclusion assay). The staining of yeast cells with calcofluor white revealed that no modification of chitin deposition pattern occurred during the exposure to metal mixture. Extending for 24 h, the exposure of yeast cells to metal mixture provoked a loss of membrane integrity, which was accompanied by the leakage of intracellular components. A marked loss of the metabolic activity and the loss of proliferation capacity were also observed. The analysis of the impact of a single metal has shown that, under the conditions studied, Pb was the metal responsible for the toxic effect observed in the metal mixture. Intracellular accumulation of Pb seems to be correlated with the metals' toxic effects observed. PMID:25794581

  2. Influence of amendments and aided phytostabilization on metal availability and mobility in Pb/Zn mine tailings.

    PubMed

    Lee, Sang-Hwan; Ji, WonHyun; Lee, Won-Seok; Koo, Namin; Koh, Il Ha; Kim, Min-Suk; Park, Jeong-Sik

    2014-06-15

    A greenhouse experiment was conducted to evaluate the effect of four different amendments, bone mill, bottom ash, furnace slag, and red mud, as immobilizing agents and the plant species Miscanthus sinensis and Pteridium aquilinum in aided phytostabilization of Pb/Zn mine tailings. The effects of amendments and plants on the availability and mobility of heavy metals were evaluated using single extraction, sequential extraction, pore-water analysis, and determination of heavy metal concentrations in plants. The application of Fe-rich amendments significantly reduced the amount of soluble and extractable heavy metals in the tailings (p < 0.05). Furnace slag and M. sinensis reduced CaCl2-extractable heavy metals by 56-91%, red mud and P. aquilinum treatment was the most effective at decreasing bioaccessible Pb, reducing it to 34% of the total Pb. Compared to control, water soluble Cd, Cu, Pb, and Zn were reduced by 99, 99, 98, and 99%, respectively, in the red mud and P. aquilinum tailings. M. sinensis accumulated heavy metals mainly in the root, and had lower translocation factors compared with P. aquilinum. The results of this study suggest that M. sinensis can be used in aided phytostabilization for these types of mine tailings and Fe-rich amendments are effective for the in situ immobilization of metals. PMID:24681360

  3. Characterization of bacteria in the rhizosphere soils of Polygonum pubescens and their potential in promoting growth and Cd, Pb, Zn uptake by Brassica napus.

    PubMed

    Jing, Yuan Xiao; Yan, Jun Lan; He, Huai Dong; Yang, Dan Jing; Xiao, Li; Zhong, Ting; Yuan, Ming; Cai, Xin De; Li, Shu Bin

    2014-01-01

    Microbe-enhanced phytoremediation has been considered as a promising measure for the remediation of metal-contaminated soils. In this study, two bacterial strains JYX7 and JYX10 were isolated from rhizosphere soils of Polygonum pubescens grown in metal-polluted soil and identified as of Enterobacter sp. and Klebsiella sp. based on 16S rDNA sequences, respectively. JYX7 and JYX10 showed high Cd, Pb and Zn tolerance and increased water-soluble Cd, Pb and Zn concentrations in culture solution and metal-added soils. Two isolates produced plant growth-promoting substances such as indole acetic acid, siderophore, 1-aminocyclopropane-1-carboxylic deaminase, and solubilized inorganic phosphate. Based upon their ability in metal tolerance and solubilization, two isolates were further studied for their effects on growth and accumulation of Cd, Pb, and Zn in Brassica napus (rape) by pot experiments. Rapes inoculated with JYX7 and JYX10 had significantly higher dry weights, concentrations and uptakes of Cd, Pb, Zn in both above-ground and root tissues than those without inoculation grown in soils amended with Cd (25 mg kg(-1)), Pb (200 mg kg(-1)) or Zn (200 mg kg(-1)). The present results demonstrated that JYX7 and JYX10 are valuable microorganism, which can improve the efficiency of phytoremediation in soils polluted by Cd, Pb, and Zn. PMID:24912234

  4. Determination of some heavy metals (Fe, Cu, Zn and Pb) in blood by total reflection X-ray fluorescence

    NASA Astrophysics Data System (ADS)

    Bounakhla, M.; Doukkali, A.; Lalaoui, K.; Aguenaou, H.; Mokhtar, N.; Attrassi, B.

    2003-05-01

    The main purpose of this study is the interaction between nutrition (micronutrients heavy metals: Fe, Zn, Cu) and toxic heavy metals such as Pb in blood of children living in Gharb region of Morocco. This region receives all pollution carried by the Sebou river coming mainly from industrial activities. A rapid and simple analytical procedure was used for the determination of Fe, Cu and Zn trace amounts in blood by total-reflection X-ray fluorescence technique. This method is an energy dispersive XRF technique in a special geometry of primary beam, sample and detector. The sample is deposited on a plane polished surface of a suitable reflector material. It is presented as a few drops (25 μl) from a solution of blood digested in a mixture of HNO3 and H2O2 using a microwaves accelerated reaction system. The accuracy of measurements has been investigated by using certified materials. The concentration of Cu was found to be normal in all samples (\\cong1 ppm) which ruled out any interaction between this element and the others. On the other hand, amounts of Fe and Zn are very variables, suggesting an interaction between Fe and Zn. However, amounts of Pb in blood are inferior to 50 ppb, suggesting that no interaction exist with this metal and micronutrients.

  5. Nanocrystal growth and morphology of PbTeSe-ZnSe composite thin films prepared by one-step synthesis method

    NASA Astrophysics Data System (ADS)

    Sato, Kazuhisa; Abe, Seishi

    2016-10-01

    The microstructure of polycrystalline PbTe1-xSex-ZnSe composite thin films has been studied by scanning transmission electron microscopy and electron diffraction. The films were prepared by the one-step synthesis method using simultaneous evaporation of PbTe and ZnSe. The nanocrystals of PbTe1-xSex are formed in a ZnSe matrix. Tellurium concentration can be tuned by controlling the PbTe evaporation source temperatures between 753 K and 793 K. Binary PbSe nanocrystals were formed at 753 K, while ternary PbTe1-xSex nanocrystals were formed at 793 K. The nanocrystals grow in a granular shape at the initial stage of film growth, and the morphology changes to nanowire-shape as the film grows, irrespective of the Te concentration. The ternary PbTe1-xSex nanocrystals were composed of two phases with different Te concentration; Te-rich (Se-poor) granular crystals were formed near the bottom half parts of the film and Te-poor (Se-rich) nanowires were formed at the upper half parts of the film. Columnar ZnSe crystals contain high-density {111} stacking faults due to the low stacking fault energy of ZnSe. A balance of deposition and re-evaporation on the substrate during the film growth will be responsible for the resultant nanocrystal morphology.

  6. Effects of Zn2+ and Pb2+ dopants on the activity of Ga2O3-based photocatalysts for water splitting.

    PubMed

    Wang, Xiang; Shen, Shuai; Jin, Shaoqing; Yang, Jingxiu; Li, Mingrun; Wang, Xiuli; Han, Hongxian; Li, Can

    2013-11-28

    Zn-doped and Pb-doped β-Ga2O3-based photocatalysts were prepared by an impregnation method. The photocatalyst based on the Zn-doped β-Ga2O3 shows a greatly enhanced activity in water splitting while the Pb-doped β-Ga2O3 one shows a dramatic decrease in activity. The effects of Zn(2+) and Pb(2+) dopants on the activity of Ga2O3-based photocatalysts for water splitting were investigated by HRTEM, XPS and time-resolved IR spectroscopy. A ZnGa2O4-β-Ga2O3 heterojunction is formed in the surface region of the Zn-doped β-Ga2O3 and a slower decay of photogenerated electrons is observed. The ZnGa2O4-β-Ga2O3 heterojunction exhibits type-II band alignment and facilitates charge separation, thus leading to an enhanced photocatalytic activity for water splitting. Unlike Zn(2+) ions, Pb(2+) ions are coordinated by oxygen atoms to form polyhedra as dopants, resulting in distorted surface structure and fast decay of photogenerated electrons of β-Ga2O3. These results suggest that the Pb dopants act as charge recombination centers expediting the recombination of photogenerated electrons and holes, thus decreasing the photocatalytic activity.

  7. Effects of Zn2+ and Pb2+ dopants on the activity of Ga2O3-based photocatalysts for water splitting.

    PubMed

    Wang, Xiang; Shen, Shuai; Jin, Shaoqing; Yang, Jingxiu; Li, Mingrun; Wang, Xiuli; Han, Hongxian; Li, Can

    2013-11-28

    Zn-doped and Pb-doped β-Ga2O3-based photocatalysts were prepared by an impregnation method. The photocatalyst based on the Zn-doped β-Ga2O3 shows a greatly enhanced activity in water splitting while the Pb-doped β-Ga2O3 one shows a dramatic decrease in activity. The effects of Zn(2+) and Pb(2+) dopants on the activity of Ga2O3-based photocatalysts for water splitting were investigated by HRTEM, XPS and time-resolved IR spectroscopy. A ZnGa2O4-β-Ga2O3 heterojunction is formed in the surface region of the Zn-doped β-Ga2O3 and a slower decay of photogenerated electrons is observed. The ZnGa2O4-β-Ga2O3 heterojunction exhibits type-II band alignment and facilitates charge separation, thus leading to an enhanced photocatalytic activity for water splitting. Unlike Zn(2+) ions, Pb(2+) ions are coordinated by oxygen atoms to form polyhedra as dopants, resulting in distorted surface structure and fast decay of photogenerated electrons of β-Ga2O3. These results suggest that the Pb dopants act as charge recombination centers expediting the recombination of photogenerated electrons and holes, thus decreasing the photocatalytic activity. PMID:24121670

  8. Diffusion across the modified polyethylene separator GX in the heat-sterilizable AgO-Zn battery

    NASA Technical Reports Server (NTRS)

    Lutwack, R.

    1973-01-01

    Models of diffusion across an inert membrane have been studied using the computer program CINDA. The models were constructed to simulate various conditions obtained in the consideration of the diffusion of Ag (OH)2 ions in the AgO-Zn battery. The effects on concentrations across the membrane at the steady state and on the fluxout as a function of time were used to examine the consequences of stepwise reducing the number of sources of ions, of stepwise blocking the source and sink surfaces, of varying the magnitude of the diffusion coefficient for a uniform membrane, of varying the diffusion coefficient across the membrane, and of excluding volumes to diffusion.

  9. Lead isotope study of Zn-Pb ore deposits associated with the Basque-Cantabrian basin and Paleozoic basement, Northern Spain

    NASA Astrophysics Data System (ADS)

    Velasco, F.; Pesquera, A.; Herrero, J. M.

    1996-01-01

    A total of forty-three galena samples from syngenetic and epigenetic Pb-Zn mineralizations emplaced in the Lower Cretaceous Basque-Cantabrian basin and Paleozoic basement of the Cinco Villas massif in the western Pyrenees, have been analyzed for Pb-isotopic composition. Galena from sedex mineralizations hosted in Carboniferous clastic rocks in the Cinco Villas massif display an homogeneous lead isotopic signature (206Pb/2044Pb ≈ 18.43, 207Pb/204Pb ≈ 15.66, 208Pb/ 204Pb ≈ 38.69) suggesting a single lead reservoir. These values are slightly more radiogenic than lead from other European Hercynian deposits, possibly reflecting the influence of a more evolved upper crustal source. Underlying Paleozoic sediments are proposed as lead source for the Cinco Villas massif ores. Analyses from twenty-six galena samples from the four strata-bound ore districts hosted in Mesozoic rocks reveal the existence of two populations regarding their lead isotopic composition. Galena from the western Santander districts (e.g., Reocin) is characterized by more radiogenic isotope values (206Pb/204Pb ≈ 18.74, 207Pb/204Pb ≈ 15.67, 208Pb/ 204Pb ≈ 38.73) than those from the central and eastern districts (Troya-Legorreta, Central and Western Vizcaya, 206Pb/204Pb ≈ 18.59, 207Pb/204Pb ≈ 15.66, 208Pb/ 204Pb ≈ 38.73). In all districts, the most likely source for these mineralizations was the thick sequence of Lower Cretaceous clastic sediments. The existence of two separate lead isotopic populations could be the result of regional difference in the composition of the basement rocks and the clastic sediments derived of it or different evolution histories. In both sub-basins, isotopic ratios indicate an increase in crustal influence as the age of the ores decreases.

  10. Highly enhanced photoluminescence of AgInS2/ZnS quantum dots by hot-injection method

    NASA Astrophysics Data System (ADS)

    Liao, Shenghua; Huang, Yu; Zhang, Ying; Shan, Xiaohui; Yan, Zhengyu; Shen, Weiyang

    2015-01-01

    Highly photoluminescent and air-stable AgInS2 quantum dots (AIS QDs) were synthesized by a hot-injection route in N2 atmosphere and dark environment. The as-synthesized AIS QDs were further capped with ZnS shell by one-pot method in order to enhance the photoluminescence (PL) intensity. The photo-electronic property and the morphology of AIS QDs and AIS/ZnS QDs were characterized by ultraviolet-visible spectroscopy (UV), PL spectroscopy and transmission electronic microscopy (TEM). The results indicated that the narrow and symmetrical PL spectra of AIS QDs was time-dependent, and the emission wavelength of AIS QDs could be tunable within 436-610 nm by altering the initial Ag/In ratios. After being capped with ZnS shell, the AIS QDs showed excellent optical characteristics, including PL QYs up to 15%. The TEM results indicated that the spherical AIS/ZnS QDs were nearly monodispersed and homogeneous with an average particle size of 8 nm. The heavy metal free and high luminous AIS/ZnS QDs have great potential in biological application.

  11. Ultrasonic-assisted preparation of novel ternary ZnO/Ag3VO4/Ag2CrO4 nanocomposites and their enhanced visible-light activities in degradation of different pollutants

    NASA Astrophysics Data System (ADS)

    Pirhashemi, Mahsa; Habibi-Yangjeh, Aziz

    2016-05-01

    Novel ternary ZnO/Ag3VO4/Ag2CrO4 nanocomposites were successfully fabricated via preparation of ZnO/Ag3VO4 followed by coupling of it with Ag2CrO4 through facile ultrasonic-assisted method. The resultant samples were carefully characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, energy dispersive analysis of X-rays, UV-vis diffuse reflectance spectroscopy, Fourier transform-infrared spectroscopy, and photoluminescence techniques. Photocatalytic activity for degradation of organic dyes, including rhodamine B, methylene blue, and methyl orange was examined under visible-light irradiation. Among the prepared samples, the ternary nanocomposite with 20% of Ag2CrO4 demonstrated the superior activity. This nanocomposite showed 10.6, 2.9, and 3.0-folds greater activity compared to ZnO, ZnO/Ag2CrO4, and ZnO/Ag3VO4, respectively. The enhanced activity was attributed to more harvesting of the visible-light irradiation and efficiently separation of the photogenerated charge carriers in the ternary nanocomposites. To understand efficiently separation of the charge carriers, a plausible diagram was proposed based on formation of tandem n-n heterojunctions.

  12. Understanding nanostructures in thermoelectric materials: an electron microscopy study of AgPb{sub 18}SbSe{sub 20} crystals.

    SciTech Connect

    Lioutas, C. B.; Frangis, N.; Todorov, I.; Chung, D. Y.; Kanatzidis, M. G.; Materials Science Division; Aristotle Univ. Thessaloniki; Northwestern Univ.

    2010-01-01

    The characterization and understanding of the presence of nanostructuring in bulk thermoelectric materials requires real space atomic level information. We report electron diffraction and high-resolution transmission electron microscopy studies of crystals of the system AgPb{sub 18}SbSe{sub 20} (=18PbSe + AgSbSe{sub 2}) which reveal that this system is nanostructured rather than a solid solution. Nanocrystals of varying sizes are found, endotaxially grown in the matrix of PbSe (phase A), and consist of two phases, a cubic one (phase B) and a tetragonal one (phase C). Well-defined coherent interfaces between the phases in the same nanocrystals are observed. On the basis of the results of combined electron crystallography techniques, we propose reasonable structural models for the phases B and C. There are significant differences in the nanostructuring chemistry between AgPb{sub 18}SbSe{sub 20} and the telluride analog AgPb{sub 18}SbTe{sub 20} (LAST-18).

  13. Nonresonant surface-enhanced Raman scattering of ZnO quantum dots with Au and Ag nanoparticles.

    PubMed

    Rumyantseva, Anna; Kostcheev, Sergey; Adam, Pierre-Michel; Gaponenko, Sergey V; Vaschenko, Svetlana V; Kulakovich, Olga S; Ramanenka, Andrey A; Guzatov, Dmitry V; Korbutyak, Dmytro; Dzhagan, Volodymyr; Stroyuk, Alexander; Shvalagin, Vitaliy

    2013-04-23

    Pronounced 10(4)-fold enhancement of Raman scattering has been obtained for ZnO nanocrystals on substrates coated with 50 nm Ag nanoparticles under nonresonant excitation with a commercial red-emitting laser. This makes feasible beyond 10(-18) mole detection of ZnO nanocrystals with a commercial setup using a 0.1 mW continuous wave laser and can be purposefully used in analytical applications where conjugated nanocrystals serve as Raman markers. For Au-coated surfaces the enhancement is much lower and the heating effects in the course of Raman experiments are pronounced.

  14. Investigation of nanostructured Pd-Ag/n-ZnO thin film based Schottky junction for methane sensing

    NASA Astrophysics Data System (ADS)

    Roy, S.; Das, S.; Sarkar, C. K.

    2016-07-01

    Undoped nanocrystalline n-type ZnO thin film was deposited by chemical deposition technique on a thermally oxidized p-Si (~5 Ω cm resistivity and <100> orientation) substrate. Formation of stable zinc oxide thin film was confirmed by two-dimensional X-Ray Diffraction (XRD) and EDX analysis. The average crystallite size of the ZnO sample was evaluated as ~50 nm. The surface was characterized by Field Emission Scanning Electron Microscopy (FESEM) and Atomic Force Microscopy (AFM) that confirm the formation of nanocrystalline (grain size ~50 nm) ZnO thin film with surface roughness of ~100 nm. Good conversion of precursor into ZnO thin film in the chemical deposition method was evident by Fourier Transform Infrared Spectroscopy (FTIR). A small peak at 479 cm-1was observed in the FTIR spectrum confirming the formation of quartzite structure of the ZnO. The band gap (~3.44 eV) of the material was calculated from the optical absorption spectroscopy. To prepare Pd-Ag/n-ZnO Schottky junction, Pd-Ag contacts were taken by electron beam evaporation method. I-V characteristics of the junction were studied at different temperatures in inert and reducing ambient (N2 and N2 + CH4) with turn on voltage of around 0.2 V. The parameters like ideality factor ( η), saturation current ( I 0), series resistance ( Rs), and barrier height ( Φ BO) of the junction were calculated in the temperature range 50-200 °C in N2 as well as in 1 % CH4 + N2 ambient. It was observed that the ideality factor decreases in the temperature range 50-200 °C ( η = 12.34 at 50 °C and η = 1.52 at 200 °C) in N2 ambient and η = 1.18 in N2 +CH4 ambient at 200 °C. Schottky Barrier Height ( Φ BO) of the Pd-Ag/n-ZnO junction was found to increase with temperature. A close observation of Pd-Ag/n-ZnO junction in the presence of methane was performed to appreciate its application as methane sensor. The sensing mechanism was illustrated by a simplified energy band diagram.

  15. Aqueous synthesis of high bright and tunable near-infrared AgInSe2-ZnSe quantum dots for bioimaging.

    PubMed

    Che, Dongchen; Zhu, Xiaoxu; Wang, Hongzhi; Duan, Yourong; Zhang, Qinghong; Li, Yaogang

    2016-02-01

    Efficient synthetic methods for near-infrared quantum dots with good biophysical properties as bioimaging agents are urgently required. In this work, a simple and fast synthesis of highly luminescent, near-infrared AgInSe2-ZnSe quantum dots (QDs) with tunable emissions in aqueous media is reported. This method avoids high temperature and pressure and organic solvents to directly generate water-dispersible AgInSe2-ZnSe QDs. The photoluminescence emission peak of the AgInSe2-ZnSe QDs ranged from 625 to 940nm, with quantum yields up to 31%. The AgInSe2-ZnSe QDs with high quantum yield, near-infrared and low cytotoxic could be used as good cell labels, showing great potential applications in bio-imaging.

  16. Aqueous synthesis of high bright and tunable near-infrared AgInSe2-ZnSe quantum dots for bioimaging.

    PubMed

    Che, Dongchen; Zhu, Xiaoxu; Wang, Hongzhi; Duan, Yourong; Zhang, Qinghong; Li, Yaogang

    2016-02-01

    Efficient synthetic methods for near-infrared quantum dots with good biophysical properties as bioimaging agents are urgently required. In this work, a simple and fast synthesis of highly luminescent, near-infrared AgInSe2-ZnSe quantum dots (QDs) with tunable emissions in aqueous media is reported. This method avoids high temperature and pressure and organic solvents to directly generate water-dispersible AgInSe2-ZnSe QDs. The photoluminescence emission peak of the AgInSe2-ZnSe QDs ranged from 625 to 940nm, with quantum yields up to 31%. The AgInSe2-ZnSe QDs with high quantum yield, near-infrared and low cytotoxic could be used as good cell labels, showing great potential applications in bio-imaging. PMID:26513730

  17. Use of Solen brevis as a biomonitor for Cd, Pb and Zn on the intertidal zones of Bushehr-Persian Gulf, Iran.

    PubMed

    Salahshur, Sara; Bakhtiari, Alireza Riyahi; Kochanian, Preeta

    2012-06-01

    The concentrations of Zn, Cd and Pb were determined in tissues (shell and soft tissue) of 144 of bivalve mollusks (Solen brevis) and 15 samples of surface sediment collected from three locations in intertidal zones of Bushehr coast, Persian Gulf, Iran in May 2011. The mean concentrations of Zn, Cd and Pb in the sediment samples were 26.2, 1.25, and 21.1 μg/g dw, respectively. The mean levels of Zn, Cd and Pb in the clam samples were 63.3, 0.67, and 4.38 μg/g dw in soft tissue and 10. 7, 1.53, and 15.6 μg/g dw in shell, respectively. The degrees of variability (CV %) for Cd and Pb within the shells were lower than for soft tissues, whereas the CV for Zn was lower in the soft tissue than in the shell, indicating that there is more precision (lower CV) in the determination of Cd and Pb in the shells and Zn in the soft tissues. Significant correlation were found between Cd (r = 0.63; p < 0.05) and Pb (r = 0.78; p < 0.01) concentrations in the shell of S. brevis and their concentrations in the surface sediments. Indeed, Zn concentrations in the soft tissue of S. brevis significantly (r = 0.63; p < 0.05) correlated with Zn concentrations in surface sediments. The results of this study suggest that the shell of S. brevis may serve as a reliable biomonitor for Cd and Pb, and the soft tissue for Zn.

  18. Valorization of a treated soil via amendments: fractionation and oral bioaccessibility of Cu, Ni, Pb, and Zn.

    PubMed

    Zagury, Gerald J; Rincon Bello, Jhony A; Guney, Mert

    2016-04-01

    The present study aims to transform a treated soil (TS) into a more desirable resource by modifying physico-chemical properties via amendments while reducing toxic metals' mobility and oral bioaccessibility. A hydrocarbon-contaminated soil submitted to treatment (TS) but still containing elevated concentrations of Cu, Ni, Pb, and Zn has been amended with compost, sand, and Al2(SO4)3 to render it usable for horticulture. Characterization and sequential extraction were performed for TS and four amended mixtures (AM1-4). P and K availability and metal bioaccessibility were investigated in TS and AM2. Amendment improved soil properties for all mixtures and yielded a usable product (AM2 20 % TS, 49 % compost, 30 % sand, 1 % Al2(SO4)3) satisfying regulatory requirements except for Pb content. In particular, AM2 had improved organic matter (OM) and cation exchange capacity (CEC), highly increased P and K availability, and reduced total metal concentrations. Furthermore, amendment decreased metal mobile fraction likely to be plant-available (in mg kg(-1), assumed as soluble/exchangeable + carbonates fractions). For AM2, estimated Pb bioavailability decreased from 1.50 × 10(3) mg kg(-1) (TS) to 238 mg kg(-1) (52.4 % (TS) to 34.2 %). Bioaccessible concentrations of Cu, Ni, and Zn (mg kg(-1)) were lower in AM2 than in TS, but there was no significant decrease for Pb. The results suggest that amendment improved soil by modifying its chemistry, resulting in lower metal mobile fraction (in %, for Cu and Zn) and bioaccessibility (in %, for Cu only). Amending soils having residual metal contamination can be an efficient valorization method, indicating potential for reducing treatment cost and environmental burden by rendering disposal/additional treatment unnecessary. Further studies including plant bioavailability are recommended to confirm results. PMID:26969154

  19. Valorization of a treated soil via amendments: fractionation and oral bioaccessibility of Cu, Ni, Pb, and Zn.

    PubMed

    Zagury, Gerald J; Rincon Bello, Jhony A; Guney, Mert

    2016-04-01

    The present study aims to transform a treated soil (TS) into a more desirable resource by modifying physico-chemical properties via amendments while reducing toxic metals' mobility and oral bioaccessibility. A hydrocarbon-contaminated soil submitted to treatment (TS) but still containing elevated concentrations of Cu, Ni, Pb, and Zn has been amended with compost, sand, and Al2(SO4)3 to render it usable for horticulture. Characterization and sequential extraction were performed for TS and four amended mixtures (AM1-4). P and K availability and metal bioaccessibility were investigated in TS and AM2. Amendment improved soil properties for all mixtures and yielded a usable product (AM2 20 % TS, 49 % compost, 30 % sand, 1 % Al2(SO4)3) satisfying regulatory requirements except for Pb content. In particular, AM2 had improved organic matter (OM) and cation exchange capacity (CEC), highly increased P and K availability, and reduced total metal concentrations. Furthermore, amendment decreased metal mobile fraction likely to be plant-available (in mg kg(-1), assumed as soluble/exchangeable + carbonates fractions). For AM2, estimated Pb bioavailability decreased from 1.50 × 10(3) mg kg(-1) (TS) to 238 mg kg(-1) (52.4 % (TS) to 34.2 %). Bioaccessible concentrations of Cu, Ni, and Zn (mg kg(-1)) were lower in AM2 than in TS, but there was no significant decrease for Pb. The results suggest that amendment improved soil by modifying its chemistry, resulting in lower metal mobile fraction (in %, for Cu and Zn) and bioaccessibility (in %, for Cu only). Amending soils having residual metal contamination can be an efficient valorization method, indicating potential for reducing treatment cost and environmental burden by rendering disposal/additional treatment unnecessary. Further studies including plant bioavailability are recommended to confirm results.

  20. Integrated readout of organic scintillator and ZnS:Ag/6LiF for segmented antineutrino detectors.

    SciTech Connect

    Kiff, Scott D.; Reyna, David; Monahan, James; Bowden, Nathaniel S.

    2010-11-01

    Antineutrino detection using inverse beta decay conversion has demonstrated the capability to measure nuclear reactor power and fissile material content for nuclear safeguards. Current efforts focus on aboveground deployment scenarios, for which highly efficient capture and identification of neutrons is needed to measure the anticipated antineutrino event rates in an elevated background environment. In this submission, we report on initial characterization of a new scintillation-based segmented design that uses layers of ZnS:Ag/{sup 6}LiF and an integrated readout technique to capture and identify neutrons created in the inverse beta decay reaction. Laboratory studies with multiple organic scintillator and ZnS:Ag/{sup 6}LiF configurations reliably identify {sup 6}Li neutron captures in 60 cm-long segments using pulse shape discrimination.

  1. Manganiferous pyroxenes and pyroxenoids from three Pb-Zn-Cu skarn deposits

    NASA Astrophysics Data System (ADS)

    Abrecht, Jürgen

    1985-05-01

    Samples from the Pb-Zn-Cu skarns of M. Ci-villina (Italy), Valle del Temperino (Italy), and Empire Mine (New Mexico, USA) have been analysed for their pyroxenes and pyroxenoids. The samples were collected immediately adjacent to the marble-skarn replacement front. All contain manganiferous pyroxenoids and manganeserich Ca-pyroxenes. The pyroxenes from each deposit form distinct groups of compositions within the diopside-hedenbergite-johannsenite triangle, with no apparent miscibility gap. Diopside contents usually are below 15 mole percent. Fibrous bustamite occurs as monomineralic zones in the Empire and in the Temperino deposit. Although rhodonite may be a primary phase in some samples from the Empire Mine, it is commonly of secondary origin in the Empire Mine and in the Civillina deposit. Its formation from manganiferous clinopyroxenes is either due to increasing Mn activity in the hydrothermal skarn solution or to higher X(CO2) in the vapour phase. When rhodonite is formed within clinopyroxenes as submicroscopic lamellae that eventually replace the whole host crystal, resulting compositions lie in the miscibility gap between rhodonite and bustamite. Textural relations indicate the replacement reaction: johannsenite + CO2 = rhodonite + calcite + quartz. Equilibrium temperatures for this reaction have been calculated by using estimated thermochemical data for johannsenite, giving a T(eq)=385° C for X(CO2)=0.1 at P(tot)= 1 kbar. Taking into consideration the reduced activity of Mn in rhodonite and of Ca in calcite, both buffered by the johannsenite, the temperature is increased for about 15° C at X(CO2)=0.01. At lower temperatures, where johannsenite is stable, the X(CO2) is confined to values below 0.01. Despite the mineralogical similarities of the three deposits differences in the development of the manganiferous skarns can be depicted.

  2. Biomimetic Method To Assemble Nanostructured Ag@ZnO on Cotton Fabrics: Application as Self-Cleaning Flexible Materials with Visible-Light Photocatalysis and Antibacterial Activities.

    PubMed

    Manna, Joydeb; Goswami, Srishti; Shilpa, Nagaraju; Sahu, Nivedita; Rana, Rohit K

    2015-04-22

    A bioinspired mineralization route to prepare self-cleaning cotton fabrics by functionalizing their surface with nanostructured Ag@ZnO is demonstrated herein. In a polyamine-mediated mineralization process, while the nucleation, organization and coating of ZnO is done directly from water-soluble zinc salts under mild conditions, the entrapped polyamine in the ZnO matrix acts as reducing agent to generate Ag(0) from Ag(I) at room temperature. The Ag@ZnO coated cotton fabrics are characterized by FESEM, HRTEM, XRD, and UV-vis-DRS to confirm the formation and coating of Ag@ZnO particles on individual threads of the fabric. The presence of Ag nanoparticles not only enables the ZnO-coated fabrics exhibiting improved photocatalytic property but also allows for visible-light-driven activities. Furthermore, it exhibits efficient antimicrobial activity against both Gram-positive and Gram-negative bacteria. Therefore, besides these multifunctional properties, the polyamine-mediated bioinspired approach is expected to pave way for functionalization of flexible substrates under mild conditions as desirable for the development and fabrication of smart, lightweight, and wearable devices for various niche applications.

  3. Zn/Ag micro-galvanic couples formed on titanium and osseointegration effects in the presence of S. aureus.

    PubMed

    Jin, Guodong; Qin, Hui; Cao, Huiliang; Qiao, Yuqin; Zhao, Yaochao; Peng, Xiaochun; Zhang, Xianlong; Liu, Xuanyong; Chu, Paul K

    2015-10-01

    Titanium implants possessing simultaneous osseointegration and antibacterial ability are desirable. In this work, three types of Zn/Ag micro-galvanic couples are fabricated on titanium by plasma immersion ion implantation to investigate the osseointegration and antibacterial effects as well as the involved mechanisms. The in vitro findings disclose enhanced proliferation, osteogenic differentiation, and gene expressions of the rat bone mesenchymal stem cells (rBMSCs), as well as good antibacterial ability on all three micro-galvanic couples. Excellent antimicrobial ability is also observed in vivo and the micro-CT and histological results reveal notable osseointegration in vivo despite the presence of bacteria. The Zn/Ag micro-galvanic couple formed on Zn/Ag dual-ion co-implanted titanium shows the best osseointegration as well as good antibacterial properties in vivo obtained from a rabbit tibia model. The difference among the three Zn/Ag micro-galvanic couples can be ascribed to the contact between the Ag NPs and Zn film, which affects the corrosion process. Our results indicate that the biological behavior can be controlled by the corrosion process of the Zn/Ag micro-galvanic couples. PMID:26141835

  4. Ternary g-C3N4/ZnO/AgCl nanocomposites: Synergistic collaboration on visible-light-driven activity in photodegradation of an organic pollutant

    NASA Astrophysics Data System (ADS)

    Akhundi, Anise; Habibi-Yangjeh, Aziz

    2015-12-01

    The present work demonstrates the preparation of ternary g-C3N4/ZnO/AgCl nanocomposites, as novel visible-light-driven photocatalysts, using a facile large-scale methodology. The microstructure, morphology, purity, thermal, and spectroscopic properties of the prepared samples were studied using XRD, TEM, EDX, TG, UV-vis DRS, FT-IR, and PL techniques. Compared with the g-C3N4/ZnO and g-C3N4/AgCl nanocomposites, the g-C3N4/ZnO/AgCl nanocomposites displayed higher photocatalytic activity for degradation of rhodamine B under visible-light irradiation. Photocatalytic activity of the g-C3N4/ZnO/AgCl (40%) nanocomposite is about 9.5, 7.5, and 6-fold higher than those of the g-C3N4, g-C3N4/ZnO, and g-C3N4/AgCl samples, respectively. The enhanced photocatalytic activity of the nanocomposites was mainly attributed to efficiently separation of the charge carriers by synergistic collaboration of ZnO and AgCl in removing photogenerated electrons from g-C3N4. Furthermore, the results showed that the photocatalytic activity of the nanocomposite considerably depends on the preparation time, calcination temperature, and scavengers of the reactive species. Finally, the nanocomposite was found to be a reusable photocatalyst.

  5. Biomimetic Method To Assemble Nanostructured Ag@ZnO on Cotton Fabrics: Application as Self-Cleaning Flexible Materials with Visible-Light Photocatalysis and Antibacterial Activities.

    PubMed

    Manna, Joydeb; Goswami, Srishti; Shilpa, Nagaraju; Sahu, Nivedita; Rana, Rohit K

    2015-04-22

    A bioinspired mineralization route to prepare self-cleaning cotton fabrics by functionalizing their surface with nanostructured Ag@ZnO is demonstrated herein. In a polyamine-mediated mineralization process, while the nucleation, organization and coating of ZnO is done directly from water-soluble zinc salts under mild conditions, the entrapped polyamine in the ZnO matrix acts as reducing agent to generate Ag(0) from Ag(I) at room temperature. The Ag@ZnO coated cotton fabrics are characterized by FESEM, HRTEM, XRD, and UV-vis-DRS to confirm the formation and coating of Ag@ZnO particles on individual threads of the fabric. The presence of Ag nanoparticles not only enables the ZnO-coated fabrics exhibiting improved photocatalytic property but also allows for visible-light-driven activities. Furthermore, it exhibits efficient antimicrobial activity against both Gram-positive and Gram-negative bacteria. Therefore, besides these multifunctional properties, the polyamine-mediated bioinspired approach is expected to pave way for functionalization of flexible substrates under mild conditions as desirable for the development and fabrication of smart, lightweight, and wearable devices for various niche applications. PMID:25823715

  6. Template free synthesis of ZnO/Ag2O nanocomposites as a highly efficient visible active photocatalyst for detoxification of methyl orange.

    PubMed

    Kadam, Abhijit; Dhabbe, Rohant; Gophane, Anna; Sathe, Tukaram; Garadkar, Kalyanrao

    2016-01-01

    A simple and effective route for the synthesis of ZnO/Ag2O nanocomposites with different weight ratios (4:1 to 4:4) have been successfully obtained by combination of thermal decomposition and precipitation technique. The structure, composition, morphology and optical properties of the as-prepared ZnO/Ag2O composites were characterized by XRD, FT-IR, EDS, SEM, TEM, UV-Vis DRS and PL, respectively. The photocatalytic performance of the photocatalysts was evaluated towards the degradation of a methyl orange (MO) under UV and visible light. More specifically, the results showed that the photocatalytic activity with highest rate constant of MO degradation over ZnO/Ag2O (4:2) nanocomposites is more than 22 and 4 times than those of pure ZnO and Ag2O under visible light irradiation, respectively. An improved photocatalytic activity was attributed to the formation of heterostructure between Ag2O and ZnO, the strong visible light absorption and more separation efficiency of photoinduced electron-hole pairs. Moreover, the ZnO/Ag2O (4:2) nanocomposite showed excellent stability towards the photodegradation of MO under visible light. Finally, a possible mechanism for enhanced charge separation and photodegrdation is proposed. Genotoxicity of MO before and after photodegradation was also evaluated by simple comet assay technique.

  7. Zn/Ag micro-galvanic couples formed on titanium and osseointegration effects in the presence of S. aureus.

    PubMed

    Jin, Guodong; Qin, Hui; Cao, Huiliang; Qiao, Yuqin; Zhao, Yaochao; Peng, Xiaochun; Zhang, Xianlong; Liu, Xuanyong; Chu, Paul K

    2015-10-01

    Titanium implants possessing simultaneous osseointegration and antibacterial ability are desirable. In this work, three types of Zn/Ag micro-galvanic couples are fabricated on titanium by plasma immersion ion implantation to investigate the osseointegration and antibacterial effects as well as the involved mechanisms. The in vitro findings disclose enhanced proliferation, osteogenic differentiation, and gene expressions of the rat bone mesenchymal stem cells (rBMSCs), as well as good antibacterial ability on all three micro-galvanic couples. Excellent antimicrobial ability is also observed in vivo and the micro-CT and histological results reveal notable osseointegration in vivo despite the presence of bacteria. The Zn/Ag micro-galvanic couple formed on Zn/Ag dual-ion co-implanted titanium shows the best osseointegration as well as good antibacterial properties in vivo obtained from a rabbit tibia model. The difference among the three Zn/Ag micro-galvanic couples can be ascribed to the contact between the Ag NPs and Zn film, which affects the corrosion process. Our results indicate that the biological behavior can be controlled by the corrosion process of the Zn/Ag micro-galvanic couples.

  8. Evidencing lead deposition at the urban scale using "short-lived" isotopic signatures of the source term (Pb-Zn refinery)

    NASA Astrophysics Data System (ADS)

    Franssens, Matthias; Flament, Pascal; Deboudt, Karine; Weis, Dominique; Perdrix, Espéranza

    2004-09-01

    To demonstrate the ability of the lead isotope signature technique to evidence the spatial extent of an industrial Pb deposition plume at a local scale, dry deposition of lead in the urban environment of a Pb-Zn refinery was investigated, as a study case, using transient ("short-lived") isotopic signatures of the industrial source. Sampling campaigns were achieved in representative weather conditions, on an 8-h basis. Dry deposition rates measured downwind from refinery emissions (≈102-103 μg Pb m-2 h-1), cross-sectionally in a 3-5 km radius area around the plant, represent 10-100 times the urban background dry fallout, measured upwind, as well as fallout measured near other potential sources of anthropogenic Pb. The Pb-Zn refinery isotopic signature (approx. 1.100<206Pb/207Pb<1.135) is made identifiable, using the same set of Pb and Zn ores for 2 days before sampling and during field experiments, by agreement with the executive staff of the plant. This source signature is less radiogenic than signatures of urban background Pb aerosols (1.155<206Pb/207Pb<1.165) and minor sources of Pb aerosols (1.147<206Pb/207Pb<1.165). By a simple binary mixing model calculation, we established the extension of the industrial Pb deposition plume. Fifty to eighty percents of total lead settled by the dry deposition mode, 3-4 km away from the refinery, still have an industrial origin. That represents from 40 to 80 μg Pb m-2 h-1, in an area where the blood lead level exceeds 100 μg Pb l-1 for 30% of men and 12% of women living there. We demonstrate here that stable Pb isotope analysis is able to evidence the Pb dry deposition plume in stabilised aerodynamic conditions, using a short-lived source term, suggesting that this methodology is able to furnish valuable data to validate industrial Pb aerosols dispersion models, at the urban scale.

  9. Thermoelectric properties of p-type Ag1-x(Pb1-ySny)mSb1-zTem+2

    NASA Astrophysics Data System (ADS)

    Ahn, Kyunghan; Kong, Huijun; Uher, Ctirad; Kanatzidis, Mercouri G.

    2016-10-01

    The thermoelectric properties of Ag1-x(Pb1-ySny)mSb1-zTem+2 (4≤m≤16, -0.1≤x≤0.3, 1/3≤y≤2/3, 0.2≤z≤0.4; Lead Antimony Silver Tellurium Tin, LASTT-m) compositions were investigated in the temperature range of 300 to ~670 K. All samples crystallize in the average NaCl-type structure without any noticeable second phase and exhibit very narrow bandgaps of <0.1 eV. We studied a range of m values, silver concentrations (x), Pb/Sn ratios (y), and antimony concentrations (z) to determine their effects on the thermoelectric properties. The samples were investigated as melt grown polycrystalline ingots. Varying the Ag contents, the Pb/Sn ratios, and the Sb contents off-stoichiometry allowed us to control the electrical conductivity, the Seebeck coefficient, and the thermal conductivity. The electrical conductivity tends to decrease with decreasing m values. The highest ZT of ~1.1 was achieved at ~660 K for Ag0.9Pb5Sn5Sb0.8Te12 mainly due to the very low lattice thermal conductivity of ~0.4 W/(m K) around 660 K. Also, samples with charge-balanced stoichiometries, Ag(Pb1-ySny)mSbTem+2, were studied and found to exhibit a lower power factor and higher lattice thermal conductivity than the Ag1-x(Pb1-ySny)mSb1-zTem+2 compositions.

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

    NASA Astrophysics Data System (ADS)

    Jang, Guh-Yaw; Duh, Jenq-Gong

    2005-01-01

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

  11. Ag-Modified In2O3/ZnO Nanobundles with High Formaldehyde Gas-Sensing Performance

    PubMed Central

    Fang, Fang; Bai, Lu; Song, Dongsheng; Yang, Hongping; Sun, Xiaoming; Sun, Hongyu; Zhu, Jing

    2015-01-01

    Ag-modified In2O3/ZnO bundles with micro/nano porous structures have been designed and synthesized with by hydrothermal method continuing with dehydration process. Each bundle consists of nanoparticles, where nanogaps of 10–30 nm are present between the nanoparticles, leading to a porous structure. This porous structure brings high surface area and fast gas diffusion, enhancing the gas sensitivity. Consequently, the HCHO gas-sensing performance of the Ag-modified In2O3/ZnO bundles have been tested, with the formaldehyde-detection limit of 100 ppb (parts per billion) and the response and recover times as short as 6 s and 3 s, respectively, at 300 °C and the detection limit of 100 ppb, response time of 12 s and recover times of 6 s at 100 °C. The HCHO sensing detect limitation matches the health standard limitation on the concentration of formaldehyde for indoor air. Moreover, the strategy to synthesize the nanobundles is just two-step heating and easy to scale up. Therefore, the Ag-modified In2O3/ZnO bundles are ready for industrialization and practical applications. PMID:26287205

  12. Humic acid degradation by the synthesized flower-like Ag/ZnO nanostructure as an efficient photocatalyst.

    PubMed

    Ghaneian, Mohammad Taghi; Morovati, Pouran; Ehrampoush, Mohammad Hassan; Tabatabaee, Masoumeh

    2014-01-01

    Nano-sized flower-like Ag/ZnO was synthesized by a simple method using zinc acetate and silver acetate under hydrothermal condition. Powder X-ray diffraction (PXRD) and transmission electron microscopy (TEM) were used to characterize the structure and morphology of the synthesized powder. Nano flower-like Ag/ZnO was used as a photocatalyst for degradation of humic acid in aqueous solution. The disappearance of HA was analyzed by measuring the absorbance of sample at special wavelength (254 nm). The effects of various parameters such as amount of photocatalyst, pH, initial humic acid concentration and irradiation time on degradation rate were systematically investigated. Photodegradation efficiency was small when the photolysis was carried out in the absence of Ag/ZnO and it was also negligible in the absence of light. Approximately 70% of humic acid (50 mg/L) has been eliminated after 40 minutes in the presences of catalyst (catalyst dose o.6 g/L and pH =7) and UVA irradiation. While, 100% of humic acid has been eliminated with solar irradiation. PMID:25520850

  13. Development of neutron-monitor detector using liquid organic scintillator coupled with 6Li + ZnS(Ag) Sheet.

    PubMed

    Sato, Tatsuhiko; Endo, Akira; Yamaguchi, Yasuhiro; Takahashi, Fumiaki

    2004-01-01

    A phoswitch-type detector has been developed for monitoring neutron doses in high-energy accelerator facilities. The detector is composed of a liquid organic scintillator (BC501A) coupled with ZnS(Ag) sheets doped with 6Li. The dose from neutrons with energies above 1 MeV is evaluated from the light output spectrum of the BC501A by applying the G-function, which relates the spectrum to the neutron dose directly. The dose from lower energy neutrons, on the other hand, is estimated from the number of scintillations emitted from the ZnS(Ag) sheets. Characteristics of the phoswitch-type detector were studied experimentally in some neutron fields. It was found from the experiments that the detector has an excellent property of pulse-shape discrimination between the scintillations of BC501A and the ZnS(Ag) sheets. The experimental results also indicate that the detector is capable of reproducing doses from thermal neutrons as well as neutrons with energies from one to several tens of megaelectronvolts (MeV).

  14. Localized surface plasmon resonances dominated giant lateral photovoltaic effect observed in ZnO/Ag/Si nanostructure

    PubMed Central

    Zhang, Ke; Wang, Hui; Gan, Zhikai; Zhou, Peiqi; Mei, Chunlian; Huang, Xu; Xia, Yuxing

    2016-01-01

    We report substantially enlarged lateral photovoltaic effect (LPE) in the ZnO/Ag/Si nanostructures. The maximum LPE sensitivity (55.05 mv/mm) obtained in this structure is about seven times larger than that observed in the control sample (7.88 mv/mm) of ZnO/Si. We attribute this phenomenon to the strong localized surface plasmon resonances (LSPRs) induced by nano Ag semicontinuous films. Quite different from the traditional LPE in PN junction type structures, in which light-generated carriers contributed to LPE merely depends on direct excitation of light in semiconductor, this work firstly demonstrates that, by introducing a super thin metal Ag in the interface between two different kinds of semiconductors, the nanoscale Ag embedded in the interface will produce strong resonance of localized field, causing extra intraband excitation, interband excitation and an enhanced direct excitation. As a consequence, these LSPRs dominated contributions harvest much more carriers, giving rise to a greatly enhanced LPE. In particular, this LSPRs-driven mechanism constitutes a sharp contrast to the traditional LPE operation mechanism. This work suggests a brand new LSPRs approach for tailoring LPE-based devices and also opens avenues of research within current photoelectric sensors area. PMID:26965713

  15. Localized surface plasmon resonances dominated giant lateral photovoltaic effect observed in ZnO/Ag/Si nanostructure

    NASA Astrophysics Data System (ADS)

    Zhang, Ke; Wang, Hui; Gan, Zhikai; Zhou, Peiqi; Mei, Chunlian; Huang, Xu; Xia, Yuxing

    2016-03-01

    We report substantially enlarged lateral photovoltaic effect (LPE) in the ZnO/Ag/Si nanostructures. The maximum LPE sensitivity (55.05 mv/mm) obtained in this structure is about seven times larger than that observed in the control sample (7.88 mv/mm) of ZnO/Si. We attribute this phenomenon to the strong localized surface plasmon resonances (LSPRs) induced by nano Ag semicontinuous films. Quite different from the traditional LPE in PN junction type structures, in which light-generated carriers contributed to LPE merely depends on direct excitation of light in semiconductor, this work firstly demonstrates that, by introducing a super thin metal Ag in the interface between two different kinds of semiconductors, the nanoscale Ag embedded in the interface will produce strong resonance of localized field, causing extra intraband excitation, interband excitation and an enhanced direct excitation. As a consequence, these LSPRs dominated contributions harvest much more carriers, giving rise to a greatly enhanced LPE. In particular, this LSPRs-driven mechanism constitutes a sharp contrast to the traditional LPE operation mechanism. This work suggests a brand new LSPRs approach for tailoring LPE-based devices and also opens avenues of research within current photoelectric sensors area.

  16. Localized surface plasmon resonances dominated giant lateral photovoltaic effect observed in ZnO/Ag/Si nanostructure.

    PubMed

    Zhang, Ke; Wang, Hui; Gan, Zhikai; Zhou, Peiqi; Mei, Chunlian; Huang, Xu; Xia, Yuxing

    2016-03-11

    We report substantially enlarged lateral photovoltaic effect (LPE) in the ZnO/Ag/Si nanostructures. The maximum LPE sensitivity (55.05 mv/mm) obtained in this structure is about seven times larger than that observed in the control sample (7.88 mv/mm) of ZnO/Si. We attribute this phenomenon to the strong localized surface plasmon resonances (LSPRs) induced by nano Ag semicontinuous films. Quite different from the traditional LPE in PN junction type structures, in which light-generated carriers contributed to LPE merely depends on direct excitation of light in semiconductor, this work firstly demonstrates that, by introducing a super thin metal Ag in the interface between two different kinds of semiconductors, the nanoscale Ag embedded in the interface will produce strong resonance of localized field, causing extra intraband excitation, interband excitation and an enhanced direct excitation. As a consequence, these LSPRs dominated contributions harvest much more carriers, giving rise to a greatly enhanced LPE. In particular, this LSPRs-driven mechanism constitutes a sharp contrast to the traditional LPE operation mechanism. This work suggests a brand new LSPRs approach for tailoring LPE-based devices and also opens avenues of research within current photoelectric sensors area.

  17. Localized surface plasmon resonances dominated giant lateral photovoltaic effect observed in ZnO/Ag/Si nanostructure.

    PubMed

    Zhang, Ke; Wang, Hui; Gan, Zhikai; Zhou, Peiqi; Mei, Chunlian; Huang, Xu; Xia, Yuxing

    2016-01-01

    We report substantially enlarged lateral photovoltaic effect (LPE) in the ZnO/Ag/Si nanostructures. The maximum LPE sensitivity (55.05 mv/mm) obtained in this structure is about seven times larger than that observed in the control sample (7.88 mv/mm) of ZnO/Si. We attribute this phenomenon to the strong localized surface plasmon resonances (LSPRs) induced by nano Ag semicontinuous films. Quite different from the traditional LPE in PN junction type structures, in which light-generated carriers contributed to LPE merely depends on direct excitation of light in semiconductor, this work firstly demonstrates that, by introducing a super thin metal Ag in the interface between two different kinds of semiconductors, the nanoscale Ag embedded in the interface will produce strong resonance of localized field, causing extra intraband excitation, interband excitation and an enhanced direct excitation. As a consequence, these LSPRs dominated contributions harvest much more carriers, giving rise to a greatly enhanced LPE. In particular, this LSPRs-driven mechanism constitutes a sharp contrast to the traditional LPE operation mechanism. This work suggests a brand new LSPRs approach for tailoring LPE-based devices and also opens avenues of research within current photoelectric sensors area. PMID:26965713

  18. Origin of the granites and related Sn and Pb-Zn polymetallic ore deposits in the Pengshan district, Jiangxi Province, South China: constraints from geochronology, geochemistry, mineral chemistry, and Sr-Nd-Hf-Pb-S isotopes

    NASA Astrophysics Data System (ADS)

    Xu, Bin; Jiang, Shao-Yong; Luo, Lan; Zhao, Kui-Dong; Ma, Liang

    2016-05-01

    The Pengshan Sn and Pb-Zn polymetallic deposits are located in the south margin of the Jiujiang-Ruichang (Jiurui) district of the Middle-Lower Yangtze River Metallogenic Belt in South China. Four large deposits include Huangjinwa, Zengjialong, Jianfengpo, and Zhangshiba, the former three are Sn-dominant deposits which occur as stratiform orebodies in the contact zones of the Pengshan granites and within the country rock strata, whereas Zhangshiba consists of stratiform Pb-Zn orebodies within the Precambrian metasedimentary strata. In this study, we present results on zircon U-Pb ages, major and trace elements, and mineral chemistry as well as Sr-Nd-Hf isotope data of the granites, Pb and S isotopes of both the Sn-dominant and Pb-Zn dominant deposits, and U-Pb dating of cassiterite from the Pengshan district. SHRIMP and LA-ICP-MS zircon U-Pb dating shows that the Pengshan granites were emplaced in the Early Cretaceous (129-128 Ma), which is in good agreement with the U-Pb dating (130-128 Ma) of cassiterite from the Jianfengpo Sn deposit. The Pengshan granites consist mainly of weakly peraluminous highly fractionated I-type affinity granitic rocks. Detailed elemental and isotopic data suggest that the granites formed by partial melting of Mesoproterozoic metamorphic basement materials with minor input of mantle-derived melts. The mineral chemistry of biotite demonstrates that the Pengshan granitic magma had a low oxygen fugacity, thereby precluding the tin dominantly partitioning into the rock-forming silicate minerals and favoring accumulation in the exsolved residual liquid during magma crystallization stages. Sulfur isotopes show a relatively heavy sulfur isotopic composition from 5.8 to 17.6 ‰, and no difference for sulfur isotopes between the Sn deposits (5.8-13.4 ‰, Huangjinwa, Zengjialong, Jianfengpo) and the Pb-Zn deposit (mostly 7.1-13.0 ‰, except for one 17.6 ‰, Zhangshiba). The sulfur isotope data of pyrite from the host sedimentary rocks show

  19. Potential hyperaccumulation of Pb, Zn, Cu and Cd in endurant plants distributed in an old smeltery, northeast China

    NASA Astrophysics Data System (ADS)

    Cui, Shuang; Zhou, Qixing; Chao, Lei

    2007-01-01

    The absorption and accumulation of Pb, Zn, Cu and Cd in some endurant weed plant species that survived in an old smeltery in Liaoning, China, were systematically investigated. Potential hyperaccumulative characteristics of these species were also discussed. The results showed that metal accumulation in plants differed with species, tissues and metals. Endurant weed plants growing in this contaminated site exhibited high metal adaptability. Both the metal exclusion and detoxification tolerance strategies were involved in the species studied. Seven species for Pb and four species for Cd were satisfied for the concentration time level standard for hyperaccumulator. Considering translocation factor (TF) values, one species for Pb, seven species for Zn, two species for Cu and five species for Cd possessed the characteristic of hyperaccumulator. Particularly, Abutilon theophrasti Medic, exhibited strong accumulative ability to four heavy metals. Although enrichment coefficients of all samples were lesser than 1 and the absolute concentrations didn’t reach the standard, species mentioned above were primarily believed to be potential hyperaccumulators.

  20. Resonance properties of Ag-ZnO nanostructures at terahertz frequencies

    PubMed Central

    Sanchez, John E.; Díaz de León, Ramón; Mendoza-Santoyo, Fernando; González, Gabriel; José-Yacaman, Miguel; Ponce, Arturo; González, Francisco Javier

    2015-01-01

    Nanoantennas have been fabricated by scaling down traditional antenna designs using nanolithographic techniques and testing them at different optical wavelengths, these particular nanoantennas have shown responses in a broad range of frequencies going from visible wavelengths to the range of the terahertz. Some self-assembled nanostructures exist that exhibit similar shapes and properties to those of traditional antenna structures. In this work the emission and absorption properties of self-assembled nanostructures made of zinc oxide nanorods on silver nanowires, which resemble traditional dipole antennas, were measured and simulated in order to test their antenna performance. These structures show resonant properties in the 10-120 THz range, with the main resonance at 60 THz. The radiation pattern of these nanostructures was also obtained by numerical simulations, and it is shown that it can be tailored to increase or decrease its directivity as a function of the location of the energy source of excitation. Experimental measurements were performed by Raman spectroscopy and Fourier Transform Infrared Spectroscopy (FTIR) in order to show existing vibrational frequencies at the resonant frequencies of the nanostructures, measurements were made from ~9 to 103 THz and the results were in agreement with the simulations. These characteristics make these metal-semiconductor Ag/ZnO nanostructures useful as self-assembled nanoantennas in applications such as terahertz spectroscopy and sensing at terahertz frequencies. PMID:26406710

  1. Resonance properties of Ag-ZnO nanostructures at terahertz frequencies.

    PubMed

    Sanchez, John E; Díaz de León, Ramón; Mendoza-Santoyo, Fernando; González, Gabriel; José-Yacaman, Miguel; Ponce, Arturo; González, Francisco Javier

    2015-09-21

    Nanoantennas have been fabricated by scaling down traditional antenna designs using nanolithographic techniques and testing them at different optical wavelengths, these particular nanoantennas have shown responses in a broad range of frequencies going from visible wavelengths to the range of the terahertz. Some self-assembled nanostructures exist that exhibit similar shapes and properties to those of traditional antenna structures. In this work the emission and absorption properties of self-assembled nanostructures made of zinc oxide nanorods on silver nanowires, which resemble traditional dipole antennas,