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Sample records for cadmium sulfide solar

  1. Cadmium sulfide solar cells

    NASA Technical Reports Server (NTRS)

    Stanley, A. G.

    1975-01-01

    Development, fabrication and applications of CdS solar cells are reviewed in detail. The suitability of CdS cells for large solar panels and microcircuitry, and their low cost, are emphasized. Developments are reviewed by manufacturer-developer. Vapor phase deposition of thin-film solar cells, doping and co-evaporation, sputtering, chemical spray, and sintered layers are reviewed, in addition to spray deposition, monograin layer structures, and silk screening. Formation of junctions by electroplating, evaporation, brushing, CuCl dip, and chemiplating are discussed, along with counterelectrode fabrication, VPD film structures, the Cu2S barrier layer, and various photovoltaic effects (contact photovoltage, light intensity variation, optical enhancement), and various other CdS topics.

  2. Integrated thin film cadmium sulfide solar cell module

    NASA Technical Reports Server (NTRS)

    Mickelsen, R. A.; Abbott, D. D.

    1971-01-01

    The design, development, fabrication and tests of flexible integrated thin-film cadmium sulfide solar cells and modules are discussed. The development of low cost and high production rate methods for interconnecting cells into large solar arrays is described. Chromium thin films were applied extensively in the deposited cell structures as a means to: (1) achieve high adherence between the cadmium sulfide films and the vacuum-metallized copper substrates, (2) obtain an ohmic contact to the cadmium sulfide films, and (3) improve the adherence of gold films as grids or contact areas.

  3. Simulated space environment tests on cadmium sulfide solar cells

    NASA Technical Reports Server (NTRS)

    Clarke, D. R.; Oman, H.

    1971-01-01

    Cadmium sulfide (Cu2s - CdS) solar cells were tested under simulated space environmental conditions. Some cells were thermally cycled with illumination from a Xenon-arc solar simulator. A cycle was one hour of illumination followed immediately with one-half hour of darkness. In the light, the cells reached an equilibrium temperature of 60 C (333 K) and in the dark the cell temperature dropped to -120 C (153 K). Other cells were constantly illuminated with a Xenon-arc solar simulator. The equilibrium temperature of these cells was 55 C (328 K). The black vacuum chamber walls were cooled with liquid nitrogen to simulate a space heat sink. Chamber pressure was maintained at 0.000001 torr or less. Almost all of the solar cells tested degraded in power when exposed to a simulated space environment of either thermal cycling or constant illumination. The cells tested the longest were exposed to 10.050 thermal cycles.

  4. Cadmium sulfide membranes

    DOEpatents

    Spanhel, Lubomir; Anderson, Marc A.

    1992-07-07

    A method is described for the creation of novel q-effect cadmium sulfide membranes. The membranes are made by first creating a dilute cadmium sulfide colloid in aqueous suspension and then removing the water and excess salts therefrom. The cadmium sulfide membrane thus produced is luminescent at room temperature and may have application in laser fabrication.

  5. Cadmium sulfide membranes

    DOEpatents

    Spanhel, Lubomir; Anderson, Marc A.

    1991-10-22

    A method is described for the creation of novel q-effect cadmium sulfide membranes. The membranes are made by first creating a dilute cadmium sulfide colloid in aqueous suspension and then removing the water and excess salts therefrom. The cadmium sulfide membrane thus produced is luminescent at room temperature and may have application in laser fabrication.

  6. Improved performance of carbon nanotubes—manganese doped cadmium sulfide quantum dot nanocomposite based solar cell

    NASA Astrophysics Data System (ADS)

    Kaur, Rajnish; Priya, Nidhi; Deep, Akash

    2016-01-01

    The nanocomposites of carbon nanotubes with quantum dots (MWCNT-QDS) display the capability of light induced charge dissociation and transport, which make them suitable for photovoltaic applications. The present work reports the coupling of multiwalled CNT (MWCNT) with L-cysteine (2-amino 3-mercaptopropionic acid) capped manganese doped cadmium sulfide QDs (CdS:Mn). The confirmation of the MWCNT-CdS:Mn nanocomposite formation is done with various instrumental techniques. Current-voltage studies of the MWCNT-CdS:Mn thin film indicate their semiconducting behavior. Further, cyclic voltammetry and frequency response analyses of the above MWCNT-CdS:Mn thin film have highlighted their potential application as a photoanode material in dye sanitized solar cells. It has been demonstrated that the use of MWCNT-CdS:Mn nanocomposite as a photoanode material offer better photocurrent characteristics as compared to QDS alone.

  7. Process for producing cadmium sulfide on a cadmium telluride surface

    DOEpatents

    Levi, Dean H.; Nelson, Art J.; Ahrenkiel, Richard K.

    1996-01-01

    A process for producing a layer of cadmium sulfide on a cadmium telluride surface to be employed in a photovoltaic device. The process comprises providing a cadmium telluride surface which is exposed to a hydrogen sulfide plasma at an exposure flow rate, an exposure time and an exposure temperature sufficient to permit reaction between the hydrogen sulfide and cadmium telluride to thereby form a cadmium sulfide layer on the cadmium telluride surface and accomplish passivation. In addition to passivation, a heterojunction at the interface of the cadmium sulfide and the cadmium telluride can be formed when the layer of cadmium sulfide formed on the cadmium telluride is of sufficient thickness.

  8. From front contact to back contact in cadmium telluride/cadmium sulfide solar cells: Buffer layer and interfacial layer

    NASA Astrophysics Data System (ADS)

    Roussillon, Yann

    Cadmium telluride (CdTe) polycrystalline thin film solar cells, with their near optimum direct band-gap of 1.4 eV matching almost perfectly the sun radiation spectrum, are a strong contender as a less expensive alternative, among photovoltaic materials, than the more commonly used silicon-based cells. Polycrystalline solar cells are usually deposited over large areas. Such devices often exhibit strong fluctuations (nonuniformities) in electronic properties, which originate from deposition and post-deposition processes, and are detrimental to the device performance. Therefore their effects need to be constrained. A new approach in this work was, when a CdS/CdTe solar cell is exposed to light and immersed in a proper electrolyte, fluctuations in surface potential can drive electrochemical reactions which result in a nonuniform interfacial layer that could balance the original nonuniformity. This approach improved the device efficiency for CdS/CdTe photovoltaic devices from 1--3% to 11--12%. Cadmium sulfide (CdS), used as a window layer and heterojunction partner to CdTe, is electrically inactive and absorb light energies above its band-gap of 2.4 eV. Therefore, to maximize the device efficiency, a thin US layer needs to be used. However, more defects, such as pinholes, are likely to be present in the film, leading to shunts. A resistive transparent layer, called buffer layer, is therefore deposited before CdS. A key observation was that the open-circuit voltage (Voc) for cells made using a buffer layer was high, around 800 mV, similar to cells without buffer layer after Cu doping. The standard p-n junction theory cannot explain this phenomena, therefore an alternative junction mechanism, similar to metal-insulator-semiconductor devices, was developed. Furthermore, alternative Cu-free back-contacts were used in conjunction with a buffer layer. The Voc of the devices was found to be dependent of the back contact used. This change occurs as the back-contact junction

  9. Development of copper sulfide/cadmium sulfide thin-film solar cells

    SciTech Connect

    Szedon, J.R.; Biter, W.J.; Abel, J.A.; Dickey, H.C.; Shirland, F.A.

    1981-02-27

    The purpose of this work has been to identify aspects of cell fabrication and treatment which are critical for achieving high efficiency Cu/sub 2/S/CdS solar cells. In approaching the problem several comparisons were made of the effects of specific steps in two methods of cell fabrication. These methods had previously given cells of about 6% and a maximum of 9% efficiency. Three areas requiring special attention and specific means to achieve acceptable results were identified. (1) The Cu/sub 2/S/CdS heterojunction area must be minimized. If single source evaporations of CdS are made on substrates whose temperatures (approx. 220/sup 0/C) are monitored and controlled using welded thermocouples, the CdS films will have adequately large grains (grain diameter greater than or equal to 2 ..mu..m) and will not develop significant etch pits during texturing in a mild etchant solution. (2) The termination of the wet barrier processing steps must be done carefully. An acceptable termination involves minimizing the amount of cuprous chloride retained on the cell surface during transfer to a rinsing stage while providing adequate exclusion of air from the space above the surface of the cuprous chloride solution. (3) Once formed, the Cu/sub 2/S layer should not be exposed to high temperatures (>100/sup 0/C) for long periods of time (> 5 min) if surface adsorbed moisture or oxygen are present. Heat treatments in ampoules under flowing hydrogen atmospheres should be preceded and followed by periods of at least 30 minutes at room temperature in the reducing ambient. If all these precautions are taken, wet chemical barrier processing of thermally evaporated CdS films on zinc-plated copper foil substrates yields cells of nearly 8% conversion efficiency without AR coating.

  10. Development of copper sulfide/cadmium sulfide thin-film solar cells

    SciTech Connect

    Szedon, J. R.; Biter, W. J.; Dickey, H. C.

    1982-03-08

    The most important accomplishments during this period were to demonstrate and to elucidate further the complex effects that occur during the aging of Cu/sub 2/S/CdS thin-film solar cells in flowing wet oxygen. There are two distinct effects. At constant illumination, the short-circuit current of cells aged at room temperature consistently decreases with time. The second effect, related to diode opposing current, is more involved and may result from several competing mechanisms. Over the short term (approx. 4 to 5 hours), the magnitude of diode opposing current decreases. After approx. 20 hours of aging, opposing current generally returns to the level achieved after hydrogen annealing which immediately preceded the aging sequence. Optical measurements of the spectral transmission of the Cu/sub 2/S layers in a cell content have been made using a silicon detector epoxied to the back of a CdS cell after the copper foil substrate was removed. There is no significant change in Cu/sub 2/S transmission behavior for wavelengths ranging from 525 to 1000 nm during wet-oxygen aging for periods of 2 to 36 hours. This suggests that the decrease in J/sub SC/ at constant illumination, for the aging experiments in a flowing wet-oxygen ambient, arises because of changes in minority-carrier transport properties of the Cu/sub 2/S. Before developing a method for using an epoxied silicon detector to measure optical behavior of the Cu/sub 2/S layer, we explored the possibility of using a junction-containing wafer of silicon as a substrate for deposited CdS films. Some monolithic structures were successfully fabricated. Comparisons were made of CdS grain structure details in the junction detector area and in an adjacent metallized area.

  11. Deep level study of cadmium sulfide/cadmium telluride solar cells

    NASA Astrophysics Data System (ADS)

    Komin, Valery Vitalyevich

    The goal of this project is to develop a reliable approach to characterize defects in CdTe/CdS solar cells, taking into account the requirements dictated by the polycrystallinity of the device materials, to characterize solar cells prepared in different processing conditions, to develop an understanding on how processing variations correlate with changes in the overall device performance and stability, and to develop recommendations on the optimization of processing conditions based on this analysis. Polycrystalline CdTe/CdS solar cells were studied using double boxcar deep level transient spectroscopy (DLTS) and correlation DLTS measurements to investigate the effect of the post-growth CdCl2 heat treatment, and the effect of the HgTe:Cu-doped graphite and Ni2P-based back contacts. The limitations of each deep-level characterization technique dictated by the polycrystalline nature of the CdTe/CdS heterostructure, were taken in consideration. Dark C-V, dark and illuminated J-V measurements were performed in order to monitor changes in the solar cell parameters during the deep level studies. To avoid issues associated with the metastability of some defects, all experiments were performed in the dark. Twelve traps were detected in the temperature range from 90K to 360K. Preliminary solar cell simulations using AMPS-1D were used to help understand the role of these traps in the current transport mechanism and the impact of their presence on the overall device performance. A donor-like defect with activation energy EA = 0.140 eV was identified as a chlorine-related DX2-state of (VCd2--ClTe+) complex. Its presence in the CdTe layer was associated with significant degradation of overall solar cell performance. An acceptor-like defect with activation energy EA = 0.350 was identified as a defect Cu Cd- or complex (Cui+-2Cu Cd-)-. Recommendations for processing condition optimization are made based on the results of this study.

  12. Process for producing cadmium sulfide on a cadmium telluride surface

    DOEpatents

    Levi, D.H.; Nelson, A.J.; Ahrenkiel, R.K.

    1996-07-30

    A process is described for producing a layer of cadmium sulfide on a cadmium telluride surface to be employed in a photovoltaic device. The process comprises providing a cadmium telluride surface which is exposed to a hydrogen sulfide plasma at an exposure flow rate, an exposure time and an exposure temperature sufficient to permit reaction between the hydrogen sulfide and cadmium telluride to thereby form a cadmium sulfide layer on the cadmium telluride surface and accomplish passivation. In addition to passivation, a heterojunction at the interface of the cadmium sulfide and the cadmium telluride can be formed when the layer of cadmium sulfide formed on the cadmium telluride is of sufficient thickness. 12 figs.

  13. Influence of a front buffer layer on the performance of flexible Cadmium sulfide/Cadmium telluride solar cells

    NASA Astrophysics Data System (ADS)

    Mahabaduge, Hasitha Padmika

    Cadmium telluride (CdTe) solar cells have been developing as a promising candidate for large-scale application of photovoltaic energy conversion and have become the most commercially successful polycrystalline thin-film solar module material. In scaling up from small cells to large-area modules, inevitably non-uniformities across the large area will limit the performance of the large cell or module. The effects of these non-uniformities can be reduced by introducing a thin, high-resistivity transparent buffer layer between the conductive electrodes and the semiconductor diode. ZnO is explored in this dissertation as a high-resistivity transparent buffer layer for sputtered CdTe solar cells and efficiencies over 15% have been achieved on commercially available Pilkington TEC15M glass substrates. The highest open-circuit voltage of 0.858V achieved using the optimized ZnO buffer layer is among the best reported in the literature. The properties of ZnO:Al as a buffer are also investigated. We have shown that ZnO:Al can serve both as a transparent conducting oxide layer as well as a high-resistivity transparent layer for CdTe solar cells. ZnO:Al reactively sputtered with oxygen can give the necessary resistivities that allow it to be used as a high-resistivity transparent layer. Glass is the most common choice as the substrate for solar cells fabricated in the superstrate configuration due to its transparency and mechanical rigidity. However flexible substrates offer the advantages of light weight, high flexibility, ease of integrability and higher throughput through roll-to-roll processing over glass. This dissertation presents significant improvements made to flexible CdTe solar cells reporting an efficiency of 14% on clear KaptonRTM flexible polyimide substrates. Our efficiency of 14% is, to our knowledge, the best for any flexible CdTe cell reported in literature.

  14. Impact of back-contact materials on performance and stability of cadmium sulfide/cadmium telluride solar cells

    NASA Astrophysics Data System (ADS)

    Demtsu, Samuel H.

    Thin-film CdTe based solar cells are one of the leading contenders for providing lowcost and pollution-free energy, The formation of a stable, low resistance, non-rectifying contact to p-CdTe thin-film is one of the major and critical challenges associated with this technology in the fabrication of efficient and stable solar cells. The premise of this thesis is a systematic study of the impact of back-contact materials on the initial performance and the degradation of CdS/CdTe solar cells. Two different back-contact structures that incorporate Cu as a key element are investigated in this study: (a) Cu1.4Te:HgTe-doped graphite and (b) evaporated-Cu back contacts. The effect of Cu inclusion is not limited to the back-contact layer where it is deposited. Cu is a known fast diffuser in p-CdTe, and therefore, a significant amount of Cu reaches both the CdTe and US layers. Hence, the effect of the presence of Cu on the individual layers: back-contact, the absorber (CdTe), and the window (CdS) layers is discussed respectively. The effect of different metals used to form the current-carrying electrode following the Cu layer is also evaluated. Devices are studied through current-voltage (JV) measurements at different temperatures and intensities, quantum efficiency (QE) measurements under light and voltage bias, capacitance-voltage (CV), drive-level-capacitance-profiling (DLCP), and time-resolved photoluminescence (TRPL) measurements. Numerical simulation is also used to reproduce and explain some of the experimental results. In devices made without Cu, a current-limiting effect, rollover (distortion) in the current-voltage characteristic, was observed. With the inclusion of a small amount of Cu (5-nm), however, the distortion disappeared, and higher FF was obtained. The performance of these devices was comparable to devices made with the standard Cu-doped graphite paste contacts when the same CdTe absorber is used. Small amount of Cu (5-20 nm) partially diffused into the

  15. Cadmium stannate selective optical films for solar energy applications

    NASA Technical Reports Server (NTRS)

    Haacke, G.

    1975-01-01

    Efforts concentrated on reducing the electrical sheet resistance of sputtered cadmium stannate films, installing and testing equipment for spray coating experiments, and sputter deposition of thin cadmium sulfide layers onto cadmium stannate electrodes. In addition, single crystal silicon wafers were coated with cadmium stannate. Work also continued on the development of the backwall CdS solar cell.

  16. Effects of contact-based non-uniformities in cadmium sulfide/cadmium telluride thin-film solar cells

    NASA Astrophysics Data System (ADS)

    Davies, Alan R.

    To strongly contribute to the near-term electricity supply, CdTe-based photovoltaic devices must continue to improve in performance under the constraint of simple and cost efficient fabrication methods. This dissertation focuses on characterization and modeling of devices with non-uniform performance induced by the cell contacts. Devices were obtained from a commercially viable pilot-scale fabrication system at Colorado State University. Current versus voltage (J-V), quantum efficiency (QE) and laser-beam-induced current (LBIC) were the main characterization techniques applied in this work. The p-type CdTe semiconductor has a large work-function and thus tends to form a Schottky barrier when the back-electrode is formed. A common strategy of mitigating the performance-limiting contact barrier is to prepare the CdTe surface with a chemical etch, and include Cu to reduce the effective barrier. Non-uniformity of the etch or Cu inclusion, or insufficient application of Cu can result in a non-uniform contact, with regions of high- and low-energy Schottky barriers participating in the cell performance. Barrier non-uniformities in devices with little or no Cu were identified with the LBIC measurement and a model for their influence was developed and tested using PSpice circuit modeling software. Because of their superstrate configuration, CdTe cells feature front contacts made from transparent-conducting oxides (TCOs). Fluorine-doped tin oxide (F:SnO2) is a common choice because of its availability and acceptable optical and electrical properties. When the n-CdS layer of the CdS/CdTe structure is thinned to encourage greater current generation, non-uniformities of the solar cell junction arise, as CdTe comes into sporadic contact with the TCO layer. Device simulations suggest that the SnO2/CdTe junction is weaker than CdS/CdTe because of a large conduction-band offset induced by the differing electron affinities in the heterojunction. LBIC was used to verify increasing

  17. Indium phosphide/cadmium sulfide thin-film solar cells. Quarterly report, July-October 1980

    SciTech Connect

    Zanio, K.

    1981-01-01

    InP thin films were deposited by planar reactive deposition on recrystallized CdS (RXCdS) and semi-insulating (100) InP substrates and evaluated as potential layers for an all-thin-film solar cell. One objective of this period was to grow InP on RXCdS at a substrate temperature which is high enough to permit the growth of p-type material but yet low enough to permit the epitaxial growth of large grains. Films prepared on RXCdS at approximately 330/sup 0/C contained a mixture of grains having both large and submicron lateral dimensions. Be-doped epitaxial films, deposited on semi-insulating InP at 330/sup 0/C, showed both n- and p-type behavior. Films prepared at higher temperatures with a freshly Be-charged indium source were p-type. However, at these temperatures, layers prepared after several runs with the same source were n-type. Analyses of the indium source and films were initiated to determine the cause of the transient doping.

  18. Indium phosphide/cadmium sulfide thin-film solar cells. Semiannual report, July 1980-December 1980

    SciTech Connect

    Zanio, K.

    1981-03-01

    InP thin films were deposited by planar reactive deposition on recyrstallized CdS (RXCdS) and semi-insulating (100) InP substrates and evaluated as potential layers for an all-thin-film solar cell. Films prepared on RXCdS at approximately 330/sup 0/C contained a mixture of grains having both large and submicron lateral dimensions. SIMS analysis showed the interdiffusion profiles to be well behaved and, within the resolution of the analysis, no significant difference in the profiles between structures prepared at 330/sup 0/C and 380/sup 0/C. Be-doped epitaxial films, deposited on semi-insulating InP at 330/sup 0/C, showed both n- and p-type behavior. Films prepared at higher and lower temperatures with a freshly Be-charged In source were p-type and n-type, respectively; the n-type behavior is associated with an excess of n-type native defects. SIMS analyses confirmed the presence of Be in all Be-doped films. Growth with deviation from stoichiometry was initiated at 330/sup 0/C to reduce the concentration of native defects. Growth of Be-doped films at higher substrate temperature with the same Be-doped source after several runs eventually resulted in n-type films. Analyses of the In source and films were initiated to determine the cause of the transient doping. As an alternative to Be doping, p-type Zn-doped InP films were prepared on InP semi-insulating substrates with room-temperature carrier concentration and mobilities of 6 x 10/sup 16/ cm/sup -3/, and 80 cm/sup 2//Vsec, respectively.

  19. Photoluminescence study of copper-doped cadmium-telluride and related stability issues for cadmium-sulfide/cadmium-telluride solar-cell devices

    NASA Astrophysics Data System (ADS)

    Grecu, Dan S.

    Lifetime predictions for CdTe photovoltaic modules represent a complex problem, partly due to the fact that a fundamental understanding of the CdTe material properties and device operation is far from being complete. One of the stability issues actively investigated is the use of Cu for the formation of a back contact. Cu is one of the few good p-dopants for CdTe, which, by forming a p+ layer at the surface of the CdTe, relaxes the requirement for a high work function metal at the back contact. On the other hand, it is known that Cu is a fast diffuser in CdTe and it was suggested that Cu migration within the device could lead to some of the observed degradation effects. in this work, we explore Cu states and migration effects in CdTe and CdS/CdTe devices using photoluminescence (PL) as the main investigative method. We confirm the assignment of several Cu-related PL transitions observed in the CdTe spectrum, namely, a bound exciton transition (X, CUCd) at 1.59eV and a donor-acceptor pair (DAP) (D, CuCd) at 1.45eV. In addition, we observe and characterize new effects related to Cu diffusion in CdTe: (a) the quenching of a DAP, Cd-vacancy related band, at 1.55eV, and (b) the formation of a new strong lattice-coupled transition at 1.555eV. These effects, we suggest, are consistent with Cu atoms occupying substitutional positions on the Cd sublattice and/or forming Frenkel pairs of the type CUi-VCd- with Cd vacancies. Similar spectral characteristics are observed for the low-S-content CdS-CdTe alloy existent in the vicinity of the junction in solar-cell devices. Using Cu-induced changes in the PL spectrum, we propose that Cu diffuses rapidly through an interstitial mechanism, as a positively charged ion, throughout the CdTe and possibly the CdS layer during the back-contact fabrication procedure. Applied electrical fields can reverse the direction of Cu migration leading to device performance degradation. In addition, it was found that Cu-doped CdTe samples exhibit a

  20. Process for thin film deposition of cadmium sulfide

    DOEpatents

    Muruska, H. Paul; Sansregret, Joseph L.; Young, Archie R.

    1982-01-01

    The present invention teaches a process for depositing layers of cadmium sulfide. The process includes depositing a layer of cadmium oxide by spray pyrolysis of a cadmium salt in an aqueous or organic solvent. The oxide film is then converted into cadmium sulfide by thermal ion exchange of the O.sup.-2 for S.sup.-2 by annealing the oxide layer in gaseous sulfur at elevated temperatures.

  1. Properties of reactively sputtered oxygenated cadmium sulfide (CdS:O) and their impact on CdTe solar cell performance

    SciTech Connect

    Meysing, Daniel M. Wolden, Colin A.; Griffith, Michelle M.; Mahabaduge, Hasitha; Pankow, Joel; Reese, Matthew O.; Burst, James M.; Rance, William L.; Barnes, Teresa M.

    2015-03-15

    Oxygenated cadmium sulfide (CdS:O) is commonly used as the n-type window layer in high-performance CdTe heterojunction solar cells. This layer is deposited by reactive sputtering, but the optimal amount of oxygen in the sputtering ambient is highly dependent on the specific system and process employed. In this work, the intrinsic properties of CdS:O were measured as a function of the oxygen content (0%–10%) in the sputtering ambient and correlated to device performance with the goal of better defining optimal CdS:O properties for CdTe solar cells. Optimal performance was found using CdS:O films that contained ∼40 at. % oxygen as measured by Rutherford backscattering spectrometry. X-ray photoelectron spectroscopy confirmed these results and showed that oxygen is incorporated primarily as oxygenated sulfur compounds (SO{sub x}). Device efficiency improved from 10.5% using CdS to >14% with CdS:O due largely to increases in short-circuit current density as well as a modest improvement in open-circuit voltage. The transparency of the CdS:O films was well correlated with observed improvements in blue quantum efficiency with increasing oxygen content. The optical bandgap of as-deposited CdS:O was identified as a simple metric for process optimization and transfer, with 2.8 eV being ideal for the device architecture employed.

  2. Trichosporon jirovecii-mediated synthesis of cadmium sulfide nanoparticles.

    PubMed

    El-Baz, Ashraf Farag; Sorour, Noha Mohamed; Shetaia, Youssria Mohamed

    2016-05-01

    Cadmium sulphide is one of the most promising materials for solar cells and of great interest due to its useful applications in photonics and electronics, thus the development of bio-mediated synthesis of cadmium sulphide nanoparticles (CdS NPs) is one of the essential areas in nanoparticles. The present study demonstrates for the first time the eco-friendly biosynthesis of CdS NPs using the yeast Trichosporon jirovecii. The biosynthesis of CdS NPs were confirmed by UV-Vis spectrum and characterized by X-ray diffraction assay and electron microscopy. Scanning and transmission electron microscope analyses shows the formation of spherical CdS NPs with a size range of about 6-15 nm with a mean Cd:S molar ratio of 1.0:0.98. T. jirovecii produced hydrogen sulfide on cysteine containing medium confirmed by positive cysteine-desulfhydrase activity and the colony color turned yellow on 0.1 mM cadmium containing medium. T. jirovecii tolerance to cadmium was increased by the UV treatment and three 0.6 mM cadmium tolerant mutants were generated upon the UV radiation treatment. The overall results indicated that T. jirovecii could tolerate cadmium toxicity by its conversion into CdS NPs on cysteine containing medium using cysteine-desulfhydrase as a defense response mechanism.

  3. Cadmium zinc sulfide by solution growth

    DOEpatents

    Chen, Wen S.

    1992-05-12

    A process for depositing thin layers of a II-VI compound cadmium zinc sulfide (CdZnS) by an aqueous solution growth technique with quality suitable for high efficiency photovoltaic or other devices which can benefit from the band edge shift resulting from the inclusion of Zn in the sulfide. A first solution comprising CdCl.sub.2 2.5H.sub.2 O, NH.sub.4 Cl, NH.sub.4 OH and ZnCl.sub.2, and a second solution comprising thiourea ((NH.sub.2).sub.2 CS) are combined and placed in a deposition cell, along with a substrate to form a thin i.e. 10 nm film of CdZnS on the substrate. This process can be sequentially repeated with to achieve deposition of independent multiple layers having different Zn concentrations.

  4. Preparation of mesoporous cadmium sulfide nanoparticles with moderate pore size

    SciTech Connect

    Han Zhaohui Zhu, Huaiyong; Shi, Jeffrey; Parkinson, Gordon; Lu, G.Q.

    2007-03-15

    The preparation of cadmium sulfide nanoparticles that have a moderate pore size is reported. This preparation method involves a hydrothermal process that produces a precursor mixture and a following acid treatment of the precursor to get the porous material. The majority of the particles have a pore size close to 20nm, which complements and fills in the gap between the existing cadmium sulfide materials, which usually have a pore size either less than 10nm or are well above 100nm.

  5. Cobalt-doped cadmium sulfide nanoparticles as efficient strategy to enhance performance of quantum dot sensitized solar cells

    NASA Astrophysics Data System (ADS)

    Firoozi, Najmeh; Dehghani, Hossein; Afrooz, Malihe

    2015-03-01

    In this study, we investigate the effect of Co2+ ion incorporation into CdS layer on the photovoltaic performance of quantum dot sensitized solar cell (QDSSC). Quantum dots are deposited by the successive ionic layer adsorption and reaction (SILAR) method on the mesoporous TiO2 film. The doped system modifies the structure of photoanode that leads to an increase in short circuit current density (Jsc) from 13.16 mA cm-2 to 16.6 mA cm-2 in the un-doped system. Electrochemical impedance analysis (EIS) reveals a decrease in charge transfer resistance at the TiO2/QDs/electrolyte interface that arises from the presence of an internal recombination pathway. The highest energy conversion efficiency (η) of 3.16% is obtained under standard air mass 1.5 global (AM 1.5G) simulated sun light by doping the optimized amount of Co2+ ion in CdS nanoparticles, corresponding to efficiency increment (35%) compared to the un-doped system. The origin of the increase in the efficiency is attributed to the dominance of charge collection to recombination. To further investigation of the electron transport time in the photoanode, the intensity modulated photocurrent spectroscopy (IMPS) is performed under standard conditions. Our obtained results can help to develop a simple and effective method to enhance the efficiency in the QDSSCs.

  6. A strategy to improve the energy conversion efficiency and stability of quantum dot-sensitized solar cells using manganese-doped cadmium sulfide quantum dots.

    PubMed

    Gopi, Chandu V V M; Venkata-Haritha, M; Kim, Soo-Kyoung; Kim, Hee-Je

    2015-01-14

    This article describes the effect of manganese (Mn) doping in CdS to improve the photovoltaic performance of quantum dot sensitized solar cells (QDSSCs). The performances of the QDSSCs are examined in detail using a polysulfide electrolyte with a copper sulfide (CuS) counter electrode. Under the illumination of one sun (AM 1.5 G, 100 mW cm(-2)), 10 molar% Mn-doped CdS QDSSCs exhibit a power conversion efficiency (η) of 2.85%, which is higher than the value of 2.11% obtained with bare CdS. The improved photovoltaic performance is due to the impurities from Mn(2+) doping of CdS, which have an impact on the structure of the host material and decrease the surface roughness. The surface roughness and morphology of Mn-doped CdS nanoparticles can be characterised from atomic force microscopy images. Furthermore, the cell device based on the Mn-CdS electrode shows superior stability in the sulfide/polysulfide electrolyte in a working state for over 10 h, resulting in a highly reproducible performance, which is a serious challenge for the Mn-doped solar cell. Our finding provides an effective method for the fabrication of Mn-doped CdS QDs, which can pave the way to further improve the efficiency of future QDSSCs.

  7. Epitaxial growth of cadmium sulfide films on silicon

    NASA Astrophysics Data System (ADS)

    Antipov, V. V.; Kukushkin, S. A.; Osipov, A. V.

    2016-03-01

    A 300-nm-thick cadmium sulfide epitaxial layer on silicon was grown for the first time. The grown was performed by the method of evaporation and condensation in a quasi-closed volume at a substrate temperature of 650°C and a growth time of 4 s. In order to avoid a chemical reaction between silicon and cadmium sulfide (at this temperature, the rate constant of the reaction is ~103) and to prevent etching of silicon by sulfur, a high-quality silicon carbide buffer layer ~100 nm thick was preliminarily synthesized by the substitution of atoms on the silicon surface. The ellipsometric, Raman, electron diffraction, and trace element analyses showed a high structural perfection of the CdS layer and the absence of a polycrystalline phase.

  8. High efficiency thin film cadmium telluride solar cells

    NASA Astrophysics Data System (ADS)

    Chu, T. L.; Chu, Shirley S.; Britt, J.; Chen, G.; Ferekides, C.; Schultz, N.; Wang, C.; Wu, C. Q.

    1992-12-01

    Cadmium sulfide (CdS), grown from an aqueous solution, and zinc oxide (ZnO), cadmium zinc sulfide (Cd1-xZnxS), and zinc selenide (ZnSe), deposited by metalorganic chemical vapor deposition (MOCVD), have been used as the window for thin film cadmium telluride (CdTe) solar cells. Thin film solar cells were prepared by the successive deposition of the window and p-CdTe (by MOCVD and close-spaced sublimation, CSS) on SnO2:F/glass substrates. CdS/CdTe(CSS) solar cells show considerably better characteristics than CdS/CdTe(MOCVD) solar cells because of the better microstructure of CSS CdTe films. Total area conversion efficiency of 14.6%, verified by the National Renewable Energy Laboratory, has been achieved for solar cells of about 1 cm2 area. Solar cell prepared by using ZnO, ZnSe, or Cd1-xZnxS as window have significantly lower photovoltage than CdS/CdTe solar cells.

  9. Substrate Configuration Cadmium Telluride Solar Cells

    NASA Astrophysics Data System (ADS)

    Matulionis, Ilvydas

    2002-03-01

    Cadmium telluride/cadmium sulfide substrate type thin-film solar cells were fabricated on 0.1 mm thick molybdenum and stainless steel substrates. The deposition method was radio frequency plasma sputtering in argon at pressures of 10 - 20 mTorr. The structure was: substrate/(ZnTe:N)/CdTe/CdS/TCO. The Transparent Conducting Oxide (TCO) was ITO or ZnO:Al. This is an inverted configuration compared to the conventional glass/TCO/CdS/CdTe/contact devices. Solar cells on Mo substrates exhibited up to 7.8(the highest value reported so far for this type of devices) and the cells on stainless steel or with ZnO:Al were about 3above 70shape at the red and blue edges of the spectrum show that there is less CdTe-CdS interdiffusion during the post-growth heat treatment compared to the conventional superstrate cells. This is attributed to the fully developed CdTe grains at the CdTe-CdS interface. Also, the current is limited at voltages above 0.8 V which indicates a back-diode effect at the metal-CdTe or CdS-TCO interface. Supported by the National Renewable Energy Laboratory.

  10. Room temperature chemical bath deposition of cadmium selenide, cadmium sulfide and cadmium sulfoselenide thin films with novel nanostructures

    NASA Astrophysics Data System (ADS)

    VanderHyde, Cephas A.; Sartale, S. D.; Patil, Jayant M.; Ghoderao, Karuna P.; Sawant, Jitendra P.; Kale, Rohidas B.

    2015-10-01

    A simple, convenient and low cost chemical synthesis route has been used to deposit nanostructured cadmium sulfide, selenide and sulfoselenide thin films at room temperature. The films were deposited on glass substrates, using cadmium acetate as cadmium ion and sodium selenosulfate/thiourea as a selenium/sulfur ion sources. Aqueous ammonia was used as a complex reagent and also to adjust the pH of the final solution. The as-deposited films were uniform, well adherent to the glass substrate, specularly reflective and red/yellow in color depending on selenium and sulfur composition. The X-ray diffraction pattern of deposited cadmium selenide thin film revealed the nanocrystalline nature with cubic phase; cadmium sulfide revealed mixture of cubic along with hexagonal phase and cadmium sulfoselenide thin film were grown with purely hexagonal phase. The morphological observations revealed the growth and formation of interesting one, two and three-dimensional nanostructures. The band gap of thin films was calculated and the results are reported.

  11. Selective Facet Reactivity During Cation Exchange in Cadmium Sulfide Nanorods

    SciTech Connect

    Sadtler, Bryce; Demchenko, Denis; Zheng, Haimei; Hughes, Steven; Merkle, Maxwell; Dahmen, Ulrich; Wang, Lin-Wang; Alivisatos, A. Paul

    2008-12-18

    The partial transformation of ionic nanocrystals through cation exchange has been used to synthesize nanocrystal heterostructures. We demonstrate that the selectivity for cation exchange to take place at different facets of the nanocrystal plays an important role in determining the resulting morphology of the binary heterostructure. In the case of copper I (Cu+) cation exchange in cadmium sulfide (CdS) nanorods, the reaction starts preferentially at the ends of the nanorods such that copper sulfide (Cu2S) grows inwards from either end. The resulting morphology is very different from the striped pattern obtained in our previous studies of silver I (Ag+) exchange in CdS nanorods where non-selective nucleation of silver sulfide (Ag2S) occurs. From interface formation energies calculated for several models of epitaxialconnections between CdS and Cu2S or Ag2S, we infer the relative stability of each interface during the nucleation and growth of Cu2S or Ag2S within the CdS nanorods. The epitaxial connections of Cu2S to the end facets of CdS nanorods minimize the formation energy, making these interfaces stable throughout the exchange reaction. However, as the two end facets of wurtzite CdS nanorods are crystallographically nonequivalent, asymmetric heterostructures can be produced.

  12. Cadmium Telluride, Cadmium Telluride/Cadmium Sulfide Core/Shell, and Cadmium Telluride/Cadmium Sulfide/Zinc Sulfide Core/Shell/Shell Quantum Dots Study

    NASA Astrophysics Data System (ADS)

    Yan, Yueran

    CdTe, CdTe/CdS core/shell, and CdTe/CdS/ZnS core/shell/shell quantum dots (QDs) are potential candidates for bio-imaging and solar cell applications because of some special physical properties in these nano materials. For example, the band gap energy of the bulk CdTe is about 1.5 eV, so that principally they can emit 790 nm light, which is in the near-infrared range (also called biological window). Moreover, theoretically hot exciton generated by QDs is possible to be caught since the exciton relaxation process in QDs is slower than in bulk materials due to the large intraband energy gap in QDs. In this dissertation, we have synthesized the CdTe and CdTe/CdS core/shell QDs, characterized their structure, and analyzed their photophysical properties. We used organometallic methods to synthesize the CdTe QDs in a noncoordinating solvent. To avoid being quenched by air, ligands, solvent, or other compounds, CdS shell was successfully deposited on the CdTe QDs by different methods, including the slow injection method, the successive ion layer adsorption and reaction (SILAR) method, and thermal-cycling coupled single precursor method (TC-SP). Our final product, quasi-type- II CdTe/CdS core/shell QDs were able to emit at 770 nm with a fluorescence quantum yield as high as 70%. We also tried to deposit a second shell ZnS on CdTe/CdS core/shell QDs since some compounds can quench CdTe/CdS core/shell QDs. Even though different methods were used to deposit ZnS shell on the CdTe/CdS core/shell QDs, CdTe/CdS/ZnS core/shell/shell QDs still can be quenched. Furthermore, the CdTe/CdS core/shell and CdTe/CdS/ZnS core/shell/shell QDs were transferred into aqueous phase, phosphate buffered saline or deionized water, by switching the hydrophilic ligands (thiol or PEG ligands). The thioglycolic acid (TGA)-capped CdTe/CdS core/shell QDs can be kept in aqueous phase with high fluorescence quantum yield (60%--70%) for more than two months. However, some other compounds in organic or

  13. In situ synthesis of binary cobalt-ruthenium nanofiber alloy counter electrode for electrolyte-free cadmium sulfide quantum dot solar cells

    NASA Astrophysics Data System (ADS)

    Du, Nan; Ren, Lei; Sun, Weifu; Jin, Xiao; Zhao, Qing; Cheng, Yuanyuan; Wei, Taihuei; Li, Qinghua

    2015-06-01

    A facile, low-cost and low-temperature fabrication approach of counter electrode is essential for pursuing robust photovoltaic devices. Herein, we develop a hydrothermal in situ growth of Cobalt-Ruthenium (Co-Ru) alloy nanofiber electrode for quantum dot solar cell (QDSC) applications. Colloidal CdS QDs with tunable absorption band edge are synthesized and used as light absorber. After optimizing the QDs with the highest photoluminescence quantum yield accompanied by considerable solar light absorption ability, QDSC based on Co-Ru alloy electrode delivers a much higher power conversion efficiency than its counterparts, i.e., either pure Co or Ru metal electrodes. In detail, Co-Ru alloy electrode exhibits high specific area, excellent electrical behavior, intimate interface contact, and good stability, thus leading to notable improved device performances. The impressive robust function of Co-Ru alloy with simple manufacturing procedure highlights its potential applications in robust QDSCs.

  14. Fabrication of polymer/cadmium sulfide hybrid solar cells [P3HT:CdS and PCPDTBT:CdS] by spray deposition.

    PubMed

    Kumar, Neetesh; Dutta, Viresh

    2014-11-15

    This paper investigates fabrication of surfactant free CdS nanoparticles (NPs) and application in the fabrication of P3HT:CdS and PCPDTBT:CdS bulk-heterojunction hybrid solar cells using high-throughput, large-area, low cost spray deposition technique. Both the hybrid active layers and hole transport layers are deposited by spray technique. The CdS/Poly(3-hexylthiophene-2,5-diyl) (P3HT) and CdS/Poly[2,6-(4,4-bis-(2-ethylhexyl)-4H-cyclopenta[2,1-b;3,4-b']dithiophene)-alt-4,7(2,1,3-benzothiadiazole)] (PCPDTBT) hybrid devices are fabricated by spray deposition process at optimized conditions (i.e. film thickness, spray solution volume, distance between sample and spray nozzle, substrate temperature, etc.). The power conversion efficiency of η=0.6% and 1.02% is obtained for P3HT:CdS and PCPDTBT:CdS hybrid devices, respectively. Spray coating holds significant promise as a technique capable of fabricating large-area, high performance hybrid solar cells.

  15. Titanium Dioxide/Upconversion Nanoparticles/Cadmium Sulfide Nanofibers Enable Enhanced Full-Spectrum Absorption for Superior Solar Light Driven Photocatalysis.

    PubMed

    Zhang, Fu; Zhang, Chuan-Ling; Wang, Wan-Ni; Cong, Huai-Ping; Qian, Hai-Sheng

    2016-06-22

    In this work, we demonstrate an electrospinning technique to fabricate TiO2 /upconversion nanoparticles (UCNPs)/CdS nanofibers on large scale. In addition, the as-prepared TiO2 nanofibers are incorporated with a high population of UCNPs and CdS nanospheres; this results in Förster resonance energy-transfer configurations of the UCNPs, TiO2 , and CdS nanospheres that are in close proximity. Hence, strong fluorescent emissions for the Tm(3+) ions including the (1) G4 →(3) H6 transition are efficiently transferred to TiO2 and the CdS nanoparticles through an energy-transfer process. The as-prepared TiO2 /UCNPs/CdS nanofibers exhibit full-spectrum solar-energy absorption and enable the efficient degradation of organic dyes by fluorescence resonance energy transfer between the UCNPs and TiO2 (or CdS). The UCNPs/TiO2 /CdS nanofibers may also have enhanced energy-transfer efficiency for wide applications in solar cells, bioimaging, photodynamics, and chemotherapy.

  16. Synthesis and spectroscopic characterization of cadmium sulfide nanowires

    NASA Astrophysics Data System (ADS)

    Kuthirummal, Narayanan; Reppert, Jason; Diehl, Brian; Rao, Apparao

    2009-03-01

    Pulsed laser vaporization method has been used for preparing cadmium sulfide (CdS) nanowires of 50 -- 100 nm in diameter. The morphology and crystallinity of as-prepared CdS nanowires are studied by means of X-ray diffraction, scanning electron microscopy (SEM), and high-resolution transmission electron microscopy (HRTEM). Excellent ordering of the lattice planes perpendicular to the [001] plane has been observed. Photoacoustic (PA), UV-Vis, Raman, and photoluminescence spectroscopy have been used to measure the optical properties. PA spectra yielded a steeper absorption edge for as-prepared CdS nanowires when compared to the conventional optical absorption spectrum. The increased steepness might be attributed to the well-ordered structure and size distribution. The data shows that PA spectroscopy is an excellent technique to investigate opaque and highly light scattering samples. Raman data suggests increased exciton-LO phonon coupling in CdS nanowires. The appearance of a narrow photoluminescence peak at 491 nm (FWHM of 9 nm) and the absence of emission above 500 nm demonstrate the high quality of nanowires.

  17. 3.88% efficient tin sulfide solar cells using congruent thermal evaporation.

    PubMed

    Steinmann, Vera; Jaramillo, R; Hartman, Katy; Chakraborty, Rupak; Brandt, Riley E; Poindexter, Jeremy R; Lee, Yun Seog; Sun, Leizhi; Polizzotti, Alexander; Park, Helen Hejin; Gordon, Roy G; Buonassisi, Tonio

    2014-11-26

    Tin sulfide (SnS), as a promising absorber material in thin-film photovoltaic devices, is described. Here, it is confirmed that SnS evaporates congruently, which provides facile composition control akin to cadmium telluride. A SnS heterojunction solar cell is demons trated, which has a power conversion efficiency of 3.88% (certified), and an empirical loss analysis is presented to guide further performance improvements. PMID:25142203

  18. A Satellite Borne Cadmium Sulfide Total Corpuscular Energy Detector

    NASA Technical Reports Server (NTRS)

    Freeman, John W.

    1961-01-01

    The properties of single crystals of cadmium sulfide as radiation detectors are described. It has been found possible to select crystals such that: (a) The ratio of increase of conductivity under irradiation to the rate of absorption of energy in the crystal is substantially independent of particle energy (over the examined ranges of 500 ev to 80 kev for electrons and 5 kev to 180 kev for protons) and of the magnitude of energy flux (over the range from.005 to 10 ergs/cm(sup 2 -sec); and (b) The above ration is substantially the same for protons, electrons, alpha particles, x-rays, and gamma-rays. For a driving voltage of 100 volts, typical crystal yield currents of 10(sup -7) to 10(sup- 6) amperes for each erg/cm(sup 2-sec) of energy absorbed by the crystal. The threshold of such crystal detectors (resulting from dark currents of the order of 10(sup 10 amp) is typically 10(sup -3) ergs/cm(sup 2- sec). For the selected crystals a response-temperature coefficient of -0.25% per degree centigrade is found for the temperature range -50 deg C to + 50 deg C. A description is given of a complete CdS total corpuscular energy detector for the study of geomagnetically trapped radiation by means of a satellite. The detector described has a dynamic range great than 10(sup 4), a solid angle of 10(exp -3) steradian, and a detection threshold of approximately 1 erg/cm(sup 2-sec-sterad). A similar detector employing a small magnet for the selective exclusion of electrons is also described. Noteworthy practical features of these detectors for satellite and space probe experiments are: (a) Use of bare crystals, without covering foils, in order to detect charged particles having energies as low as hundreds of electron volts. (b) Simplicity of electronic auxiliaries. (c) Compactness, lightweight and nechanical ruggedness. (d) Low electrical power requirements; and (e) Conversion of conduction current to the rate of a twostate relaxation oscillator in order to facilitate telemetric

  19. Release of dissolved cadmium and sulfur nanoparticles from oxidizing sulfide minerals

    EPA Science Inventory

    Cadmium enrichment (relative to Fe and Zn) in paddy rice grain occurs during the pre-harvest drainage of flooded soil, which causes oxidative dissolution of sulfide minerals present in reduced soil. We investigated this process over a range of environmentally realistic Cdcontain...

  20. Cadmium sulfide quantum dots induce oxidative stress and behavioral impairments in the marine clam Scrobicularia plana.

    PubMed

    Buffet, Pierre-Emmanuel; Zalouk-Vergnoux, Aurore; Poirier, Laurence; Lopes, Christelle; Risso-de-Faverney, Christine; Guibbolini, Marielle; Gilliland, Douglas; Perrein-Ettajani, Hanane; Valsami-Jones, Eugenia; Mouneyrac, Catherine

    2015-07-01

    Cadmium sulfide (CdS) quantum dots have a number of current applications in electronics and solar cells and significant future potential in medicine. The aim of the present study was to examine the toxic effects of CdS quantum dots on the marine clam Scrobicularia plana exposed for 14 d to these nanomaterials (10 µg Cd L(-1) ) in natural seawater and to compare them with soluble Cd. Measurement of labile Cd released from CdS quantum dots showed that 52% of CdS quantum dots remained in the nanoparticulate form. Clams accumulated the same levels of Cd regardless of the form in which it was delivered (soluble Cd vs CdS quantum dots). However, significant changes in biochemical responses were observed in clams exposed to CdS quantum dots compared with soluble Cd. Increased activities of catalase and glutathione-S-transferase were significantly higher in clams exposed in seawater to Cd as the nanoparticulate versus the soluble form, suggesting a specific nano effect. The behavior of S. plana in sediment showed impairments of foot movements only in the case of exposure to CdS quantum dots. The results show that oxidative stress and behavior biomarkers are sensitive predictors of CdS quantum dots toxicity in S. plana. Such responses, appearing well before changes might occur at the population level, demonstrate the usefulness of this model species and type of biomarker in the assessment of nanoparticle contamination in estuarine ecosystems. PMID:25772261

  1. Cadmium sulfide quantum dots induce oxidative stress and behavioral impairments in the marine clam Scrobicularia plana.

    PubMed

    Buffet, Pierre-Emmanuel; Zalouk-Vergnoux, Aurore; Poirier, Laurence; Lopes, Christelle; Risso-de-Faverney, Christine; Guibbolini, Marielle; Gilliland, Douglas; Perrein-Ettajani, Hanane; Valsami-Jones, Eugenia; Mouneyrac, Catherine

    2015-07-01

    Cadmium sulfide (CdS) quantum dots have a number of current applications in electronics and solar cells and significant future potential in medicine. The aim of the present study was to examine the toxic effects of CdS quantum dots on the marine clam Scrobicularia plana exposed for 14 d to these nanomaterials (10 µg Cd L(-1) ) in natural seawater and to compare them with soluble Cd. Measurement of labile Cd released from CdS quantum dots showed that 52% of CdS quantum dots remained in the nanoparticulate form. Clams accumulated the same levels of Cd regardless of the form in which it was delivered (soluble Cd vs CdS quantum dots). However, significant changes in biochemical responses were observed in clams exposed to CdS quantum dots compared with soluble Cd. Increased activities of catalase and glutathione-S-transferase were significantly higher in clams exposed in seawater to Cd as the nanoparticulate versus the soluble form, suggesting a specific nano effect. The behavior of S. plana in sediment showed impairments of foot movements only in the case of exposure to CdS quantum dots. The results show that oxidative stress and behavior biomarkers are sensitive predictors of CdS quantum dots toxicity in S. plana. Such responses, appearing well before changes might occur at the population level, demonstrate the usefulness of this model species and type of biomarker in the assessment of nanoparticle contamination in estuarine ecosystems.

  2. Hydrogen sulfide modulates cadmium-induced physiological and biochemical responses to alleviate cadmium toxicity in rice.

    PubMed

    Mostofa, Mohammad Golam; Rahman, Anisur; Ansary, Md Mesbah Uddin; Watanabe, Ayaka; Fujita, Masayuki; Tran, Lam-Son Phan

    2015-09-11

    We investigated the physiological and biochemical mechanisms by which H2S mitigates the cadmium stress in rice. Results revealed that cadmium exposure resulted in growth inhibition and biomass reduction, which is correlated with the increased uptake of cadmium and depletion of the photosynthetic pigments, leaf water contents, essential minerals, water-soluble proteins, and enzymatic and non-enzymatic antioxidants. Excessive cadmium also potentiated its toxicity by inducing oxidative stress, as evidenced by increased levels of superoxide, hydrogen peroxide, methylglyoxal and malondialdehyde. However, elevating endogenous H2S level improved physiological and biochemical attributes, which was clearly observed in the growth and phenotypes of H2S-treated rice plants under cadmium stress. H2S reduced cadmium-induced oxidative stress, particularly by enhancing redox status and the activities of reactive oxygen species and methylglyoxal detoxifying enzymes. Notably, H2S maintained cadmium and mineral homeostases in roots and leaves of cadmium-stressed plants. By contrast, adding H2S-scavenger hypotaurine abolished the beneficial effect of H2S, further strengthening the clear role of H2S in alleviating cadmium toxicity in rice. Collectively, our findings provide an insight into H2S-induced protective mechanisms of rice exposed to cadmium stress, thus proposing H2S as a potential candidate for managing toxicity of cadmium, and perhaps other heavy metals, in rice and other crops.

  3. Hydrogen sulfide modulates cadmium-induced physiological and biochemical responses to alleviate cadmium toxicity in rice

    PubMed Central

    Mostofa, Mohammad Golam; Rahman, Anisur; Ansary, Md. Mesbah Uddin; Watanabe, Ayaka; Fujita, Masayuki; Phan Tran, Lam-Son

    2015-01-01

    We investigated the physiological and biochemical mechanisms by which H2S mitigates the cadmium stress in rice. Results revealed that cadmium exposure resulted in growth inhibition and biomass reduction, which is correlated with the increased uptake of cadmium and depletion of the photosynthetic pigments, leaf water contents, essential minerals, water-soluble proteins, and enzymatic and non-enzymatic antioxidants. Excessive cadmium also potentiated its toxicity by inducing oxidative stress, as evidenced by increased levels of superoxide, hydrogen peroxide, methylglyoxal and malondialdehyde. However, elevating endogenous H2S level improved physiological and biochemical attributes, which was clearly observed in the growth and phenotypes of H2S-treated rice plants under cadmium stress. H2S reduced cadmium-induced oxidative stress, particularly by enhancing redox status and the activities of reactive oxygen species and methylglyoxal detoxifying enzymes. Notably, H2S maintained cadmium and mineral homeostases in roots and leaves of cadmium-stressed plants. By contrast, adding H2S-scavenger hypotaurine abolished the beneficial effect of H2S, further strengthening the clear role of H2S in alleviating cadmium toxicity in rice. Collectively, our findings provide an insight into H2S-induced protective mechanisms of rice exposed to cadmium stress, thus proposing H2S as a potential candidate for managing toxicity of cadmium, and perhaps other heavy metals, in rice and other crops. PMID:26361343

  4. Environmental, health, safety, and regulatory review of selected photovoltaic options: Copper sulfide/cadmium sulfide and polycrystalline silicon

    NASA Astrophysics Data System (ADS)

    Lawrence, K.; Morgan, S.; Schaller, D.; Wilczak, T.

    1981-06-01

    Emissions, effluents and solid wastes from the fabrication of both polycrystalline silicon and front-wall copper sulfide/cadmium sulfide photovoltaic cells are summarized. Environmental, health, and safety characteristics of cell fabrication material inputs and by products are listed. Candidate waste stream treatment methods and resultant effluents are reviewed. Environmental, health, and safety effects of photovoltaic cell/module/array installation, operation, maintenance, and decommission are summarized. Federal legislation is addressed and future regulatory trends under these laws as they may affect each cell process are discussed. Water quality, solid waste disposal, and occupational health and safety regulations will likely be those most applicable to commercial scale PV production. Currently available control technology appears sufficient to treat cell fabrication wastes.

  5. Enhanced photoluminescence from ordered arrays of cadmium sulfide nanotubes synthesized using nanoscale chemical reactors.

    PubMed

    Varghese, Arthur

    2014-06-01

    We report enhanced room temperature photoluminescence from ordered arrays of few micrometers long cadmium sulfide nanotubes fabricated using 'nanoscale chemical reactors' of porous alumina by a unique two-chamber synthesis without using any surfactants. Photoluminescence from these nanotubes is -20 times larger than that of nanocrystalline cadmium sulfide particles prepared by bulk mixing of the same reactants. However, we rule out any quantum size effect as a source of enhanced photoluminescence from these intentionally un-passivated nanotubes. We identify sulfur deficiency in these nanotubes and directional orientation of these ordered nanotube arrays as the main reason for its superior photoluminescence as compared to agglomerated nanocrystallites of CdS prepared by bulk mixing.

  6. Acid volatile sulfide predicts the acute toxicity of cadmium and nickel in sediments

    SciTech Connect

    Di Toro, D.M.; Mahony, J.D.; Hansen, D.J.; Scott, K.J.; Carlson, A.R.

    1991-01-01

    Laboratory toxicity tests using amphipods, oligochaetes, and snails with spiked freshwater and marine sediments and with contaminated sediments collected from an EPA Superfund site demonstrate that no significant mortality occurs relative to controls if the molar concentration of acid volatile sulfide (AVS) in the sediment is greater than the molar concentration of simultaneously extracted cadmium and/or nickel. Although it is well-known that these metals can form insoluble sulfides, it apparently has not been realized that AVS is a reactive pool of solid-phase sulfide that is available to bind metals and render that portion unavailable and nontoxic to biota. Thus, the AVS concentration of a sediment establishes the boundary below which these metals cease to exhibit an acute toxicity in freshwater and marine sediments.

  7. Cadmium-sulfide crystallites in Cd-(. gamma. EC) sub n G peptide complexes from tomato. [Lycopersicon esculentum

    SciTech Connect

    Reese, R.N.; White, C.A.; Winge, D.R. Univ. of Utah, Salt Lake City )

    1992-01-01

    Hydroponically grown tomato plants (Lycopersicon esculentum P. Mill cv Golden Boy) exposed to 100 micromolar cadmium sulfate produced metal-({gamma}EC){sub n}G peptide complexes containing acid-labile sulfur. The properties of the complexes resemble those of the cadmium-({gamma}EC){sub n}G peptide complexes from Schizo-saccharomyces pombe and Candida glabrata known to contain a cadmium sulfide crystallite core. The crystallite is stabilized by a sheath of peptides of general structure ({gamma}Glu-Cys){sub n}-Gly. The cadmium-peptide complexes of tomato contained predominantly peptides of n{sub 3}, n{sub 4}, and n{sub 5}. Spectroscopic analyses indicated that the tomato cadmium-sulfide-peptide complex contained CdS crystallite core particles smaller than 2.0 nanometers in diameter.

  8. Effects of diallyl sulfide and zinc on testicular steroidogenesis in cadmium-treated male rats.

    PubMed

    Sadik, Nermin A H

    2008-01-01

    Cadmium (Cd) is one of the environmental pollutants that affect various tissues and organs including testis. Harmful effect of cadmium on testis is known to be germ cell degeneration and impairment of testicular steroidogenesis. In the present study, the effect of diallyl sulfide (DAS), a sulfur-containing volatile compound present in garlic, and zinc (Zn) was investigated on cadmium-induced testicular toxicity in rats. Male adult Wistar rats treated with cadmium (2.5 mg/kg body wt, five times a week for 4 weeks) showed decreased body weight, paired testicular weight, relative testicular weight, serum testosterone, luteinizing hormone, follicle-stimulating hormone, and testicular total antioxidant capacity (TAC) and protein levels. Testicular steroidogenic enzymes, such as 3beta-hydroxysteroid dehydrogenase (3beta-HSD) and 17beta-hydroxysteroid dehydrogenase (17beta-HSD), and marker enzymes, such as sorbitol dehydrogenase (SDH), lactate dehydrogenase (LDH), acid phosphatase (ACP), alkaline phosphatase (ALP), and glucose-6-phosphate dehydrogenase (G6PD), showed a significant decrease in activities whereas that of gamma-glutamyl transferase was significantly increased after cadmium exposure. The results have revealed that concurrent treatment with DAS or zinc restored key steroidogenic enzymes, SDH, LDH, and G6PD and increased testicular weight significantly. DAS restored the TAC level and increased testosterone level and relative testicular weight significantly. Zinc restored testicular protein level and body weight. It can be concluded that cadmium causes testicular toxicity and inhibits androgen production in adult male rats probably by affecting pituitary gonadotrophins and that concurrent administration of DAS or zinc provides protection against cadmium-induced testicular toxicity. PMID:18972399

  9. Resonant photoactivation of cadmium sulfide and its effect on the surface chemical activity

    NASA Astrophysics Data System (ADS)

    Giberti, Alessio; Fabbri, Barbara; Gaiardo, Andrea; Guidi, Vincenzo; Malagù, Cesare

    2014-06-01

    Photo-enhanced surface chemical activity of cadmium sulfide gives rise to a wide class of surface-dependent phenomena, such as heterogeneous photocatalysis, chemoresistivity, and chemiluminescence, which have several technological and scientific applications. In this work, the photochemical properties of nanostructured cadmium sulfide films are investigated by means of electrical conductance measurements in controlled atmosphere, while irradiated by light of wavelengths ranging from 400 to 645 nm. Chemisorption of benzene, carbon monoxide, methane, ethanol, and hydrogen sulfide onto CdS surface has been analyzed as a function of the wavelength, in a gas concentration range of the order of parts per million. It resulted that the increase of photoconductance with gas adsorption is resonant with the bandgap energy. It turns out that this resonant enhancement of the surface chemical activity can be of advantage for all the optical and chemical mechanisms that depend upon it. An interpretation of these results, in terms of electronic optical transitions and Fermi level shift induced by light, is proposed.

  10. Some aspects of optical feedback with cadmium sulfide and related photoconductors. [for extended frequency response

    NASA Technical Reports Server (NTRS)

    Katzberg, S. J.

    1974-01-01

    A primary limitation of many solid state photoconductors used in electro-optical systems is their slow response in converting varying light intensities into electrical signals. An optical feedback technique is presented which can extend the frequency response of systems that use these detectors by orders of magnitude without adversely affecting overall signal-to-noise ratio performance. The technique is analyzed to predict the improvement possible and a system is implemented using cadmium sulfide to demonstrate the effectiveness of the technique and the validity of the analysis.

  11. Morphology and thermal studies of zinc sulfide and cadmium sulfide nanoparticles in polyvinyl alcohol matrix

    NASA Astrophysics Data System (ADS)

    Osuntokun, Jejenija; Ajibade, Peter A.

    2016-09-01

    Zn(II) and Cd(II) metal complexes of 1-cyano-1-carboethoxyethylene-2,2-dithiolato-κS,S'-bis(N,N-dimethylthiourea-κS) have been synthesized and characterized with analytical and spectroscopic techniques. The complexes were thermolysed in hexadecylamine at 200 °C to prepare ZnS and CdS nanoparticles. The nanoparticles were characterized with scanning electron microscope (SEM), transmission electron microscope (TEM), and powder X-ray diffraction (p-XRD). TEM images showed spherically shaped nanoparticles, whose sizes are in the range 4.33-7.21 nm for ZnS and 4.95-7.7 nm CdS respectively and XRD confirmed cubic crystalline phases for the nanoparticles. The optical band gap energy evaluated from the absorption spectra are 2.88 eV (430 nm) and 2.81 eV (440 nm) for the ZnS and CdS nanoparticles respectively. The as-prepared metal sulfide nanoparticles were further incorporated into polyvinyl alcohol (PVA) to give ZnS/PVA and CdS/PVA composites. The polymer nanocomposites were studied to investigate their morphology and thermal properties relative to the pure PVA. XRD diffractions indicated that the crystalline phases of the nanoparticles and the sizes in PVA matrices remained unaltered. Infra-red spectra studies revealed interactions between the PVA and the metal sulfide nanoparticles and TGA studies show that the ZnS/PVA and CdS/PVA nanocomposites exhibit better thermal stability than the pure PVA.

  12. Cadmium sulfide quantum dot/chitosan nanocomposites for latent fingermark detection.

    PubMed

    Dilag, Jessirie; Kobus, Hilton; Ellis, Amanda V

    2009-05-30

    The detection of latent fingermarks is a challenging task in forensic science. Here we present work using highly photoluminescent cadmium sulfide (CdS) quantum dots (QDs) encapsulated in an inexpensive biopolymeric chitosan matrix for latent fingermark detection. Cadmium ions were chelated within the chitosan matrix followed by the rapid addition of sodium sulfide to produce a CdS/chitosan nanocomposite. The average QD size was investigated as a function of precursor concentrations using ultra-violet-vis (UV-vis) spectrophotometry and the QDs were imaged with transmission electron microscopy (TEM). Fluorescence spectrophotometry of the QDs at an excitation of 450 nm showed a narrow emission at 531 nm and broad emission between 600 and 850 nm with a maximum at 716 nm. Freshly deposited latent fingermarks deposited on aluminium foil were clearly detected under a Rofin Polilight at 450 nm by dusting with a freeze-dried suspension of the CdS/chitosan nanocomposite and a surfactant, tergitol, giving a so-called quantum dot surfactant (QDS) powder.

  13. Chronic effect of cadmium in sediments on colonization by benthic marine organisms: An evaluation of the role of interstitial cadmium and acid-volatile sulfide in biological availability

    SciTech Connect

    Hansen, D.J.; Berry, W.J.; Benyi, S.J.; Mahony, J.D.; Corbin, J.M.; Pratt, S.D.; Toro, D.M. di |; Abel, M.B.

    1996-12-01

    The role of interstitial cadmium and acid-volatile sulfide (AVS) in controlling the bioavailability of sediment-associated metal was examined using the chronic saltwater benthic colonization test. Sediments were spiked to achieve nominal cadmium/AVS molar ratios of 0.0 (control), 0.1, 0.8, and 3.0 in this 118-d test. Oxidation of AVS in the surficial 2.4 cm within 2 to 4 weeks resulted in sulfide profiles similar to those occurring naturally in local sediments. In the nominal 0.1 cadmium/AVS treatment measured simultaneously extracted metal (SEM{sub Cd}) was always less than AVS. Interstitial cadmium concentrations were less than those likely to cause biological effects. No significant biological effects were detected. In the nominal 0.8 cadmium/AVS treatment, measured SEM{sub Cd} commonly exceeded AVS in the surficial 2.4 cm of sediment. Interstitial cadmium concentrations were of likely toxicological significance to highly sensitive species. Shifts in the presence or absence over all taxa, and fewer macrobenthic polychaetes (Mediomastus ambiseta, Streblospio benedicti, and Podarke obscurea) and unidentified meiofaunal nematodes, were observed. In the nominal 3.0 cadmium/AVS treatment, concentrations of SEM{sub Cd} were always greater than AVS throughout the sediment column. Interstitial cadmium ranged from 28,000 to 174,000 {micro}g/L. In addition to the effects above, the sediments were colonized by fewer macrobenthic species, polychaete species, and harpacticoids; had lower densities of diatoms; lacked bivalve molluscs; and exhibited other impacts. Over all treatments, the observed biological responses were consistent with SEM{sub Cd}/AVS ratios in surficial sediments and interstitial water cadmium concentrations.

  14. Aerobic transformation of cadmium through metal sulfide biosynthesis in photosynthetic microorganisms

    PubMed Central

    2013-01-01

    Background Cadmium is a non-essential metal that is toxic because of its interference with essential metals such as iron, calcium and zinc causing numerous detrimental metabolic and cellular effects. The amount of this metal in the environment has increased dramatically since the advent of the industrial age as a result of mining activities, the use of fertilizers and sewage sludge in farming, and discharges from manufacturing activities. The metal bioremediation utility of phototrophic microbes has been demonstrated through their ability to detoxify Hg(II) into HgS under aerobic conditions. Metal sulfides are generally very insoluble and therefore, biologically unavailable. Results When Cd(II) was exposed to cells it was bioconverted into CdS by the green alga Chlamydomonas reinhardtii, the red alga Cyanidioschyzon merolae, and the cyanobacterium, Synechoccocus leopoliensis. Supplementation of the two eukaryotic algae with extra sulfate, but not sulfite or cysteine, increased their cadmium tolerances as well as their abilities to produce CdS, indicating an involvement of sulfate assimilation in the detoxification process. However, the combined activities of extracted serine acetyl-transferase (SAT) and O-acetylserine(thiol)lyase (OASTL) used to monitor sulfate assimilation, was not significantly elevated during cell treatments that favored sulfide biosynthesis. It is possible that the prolonged incubation of the experiments occurring over two days could have compensated for the low rates of sulfate assimilation. This was also the case for S. leopoliensis where sulfite and cysteine as well as sulfate supplementation enhanced CdS synthesis. In general, conditions that increased cadmium sulfide production also resulted in elevated cysteine desulfhydrase activities, strongly suggesting that cysteine is the direct source of sulfur for CdS synthesis. Conclusions Cadmium(II) tolerance and CdS formation were significantly enhanced by sulfate supplementation, thus

  15. Biocatalytic etching of semiconductor cadmium sulfide nanoparticles as a new platform for the optical detection of analytes.

    PubMed

    Grinyte, R; Saa, L; Garai-Ibabe, G; Pavlov, V

    2015-12-14

    We report for the first time the enzymatic etching of cadmium sulfide nanoparticles (CdS NPs). The fluorescence of semiconductor CdS NPs is modulated irreversibly by an enzymatic reaction catalyzed by horseradish peroxidase (HRP). We observed blue-shifts of the corresponding fluorescence peaks for CdS NPs and a decrease in the intensity of the fluorescence signal.

  16. Cadmium sulfide/copper sulfide heterojunction cell research. Technical progress report, September 1-November 30, 1979

    SciTech Connect

    Anderson, W.W.; Jonath, A.D.

    1980-02-01

    Several all sputter deposited Cu/sub 2/S/CdS cells have been prepared to date with J/sub SC/ approx. = 3 mA/cm/sup 2/ under simulated AM1 illumination. The best AM1 conversion efficiency obtained is 0.6%. This is shown to be typical of sputtered CdS in Cu/sub 2/S/CdS cells investigated to date. The sputtered Cu/sub 2/S appears to be satisfactory for solar cell applications. Presented evidence indicates that the poor conversion efficiency is due to a low-junction electric field intensity on the CdS side of the heterojunction. A multilayer CdS structure has been developed which may allow the tailoring of the junction electric field intensity to a selected high value to obtain high-junction collection efficiency. Other areas of cell development advances included: (1) determination of effect of Cu cones in Cu/sub 2/S on Cu/sub 2/S/CdS cell performance; (2) solution of CdS pinhole problem; and (3) open circuit voltage improvement by heat treatment.

  17. The synthesis of cadmium sulfide nanoplatelets using a novel continuous flow sonochemical reactor

    DOE PAGESBeta

    Palanisamy, Barath; Paul, Brian; Chang, Chih -hung

    2015-01-21

    A continuous flow sonochemical reactor was developed capable of producing metastable cadmium sulfide (CdS) nanoplatelets with thicknesses at or below 10 nm. The continuous flow sonochemical reactor included the passive in-line micromixing of reagents prior to sonochemical reaction. Synthesis results were compared with those from reactors involving batch conventional heating and batch ultrasound-induced heating. The continuous sonochemical synthesis was found to result in high aspect ratio hexagonal platelets of CdS possessing cubic crystal structures with thicknesses well below 10 nm. The unique shape and crystal structure of the nanoplatelets are suggestive of high localized temperatures within the sonochemical process. Asmore » a result, the particle size uniformity and product throughput are much higher for the continuous sonochemical process in comparison to the batch sonochemical process and conventional synthesis processes.« less

  18. Structural and chemical properties of highly oriented cadmium sulfide (CdS) cauliflower films

    NASA Astrophysics Data System (ADS)

    Vemuri, R. S.; Gullapalli, S. K.; Zubia, D.; McClure, J. C.; Ramana, C. V.

    2010-08-01

    Cadmium sulfide (CdS) films have been produced by sputter-deposition varying the sputtering-power ( P) in the range of 60-120 W. The crystal structure, morphology and chemical quality of the CdS films has been investigated employing X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), and X-ray spectrometry (EDS). Structural characterization indicates that all the CdS layers exhibit cauliflower morphology. Highly oriented, single phase hexagonal-CdS films can be produced at P = 75-105 W while the films at other power contain mixed phases. Characterization using XPS and EDS indicate that the CdS layers are nearly stoichiometric at P = 75-105 W, at which point S-deficiency is induced resulting in Cd-rich-CdS layers.

  19. The Potential Application of Raw Cadmium Sulfide Nanoparticles as CT Photographic Developer

    NASA Astrophysics Data System (ADS)

    Wu, Qiang; Huang, Lingxin; Li, Zhan; An, Wenzhen; Liu, Dan; Lin, Jin; Tian, Longlong; Wang, Xinling; Liu, Bo; Qi, Wei; Wu, Wangsuo

    2016-04-01

    With the development of science and technology, new applications about nanoparticles should be explored to achieve full-scale knowledge. Therefore, in this work, the toxicity and potential application of raw cadmium sulfide nanoparticles (CdS) in vivo were further studied through ICP-OES and CTs. Surprisingly, CdS exhibited an excellent photographic property, except for finding the accumulation of CdS in the lungs, liver, spleen, and kidney with a strong dependence on time; it is also found that there were a significant uptake in the pancreas for an obvious CT imaging. And the following investigations showed that the raw CdS could damage the tissues accumulating nanoparticles. Through this work, it can be seen that the raw CdS being modified might be an excellent photographic developer for detecting cancers or other diseases.

  20. The Potential Application of Raw Cadmium Sulfide Nanoparticles as CT Photographic Developer.

    PubMed

    Wu, Qiang; Huang, Lingxin; Li, Zhan; An, Wenzhen; Liu, Dan; Lin, Jin; Tian, Longlong; Wang, Xinling; Liu, Bo; Qi, Wei; Wu, Wangsuo

    2016-12-01

    With the development of science and technology, new applications about nanoparticles should be explored to achieve full-scale knowledge. Therefore, in this work, the toxicity and potential application of raw cadmium sulfide nanoparticles (CdS) in vivo were further studied through ICP-OES and CTs. Surprisingly, CdS exhibited an excellent photographic property, except for finding the accumulation of CdS in the lungs, liver, spleen, and kidney with a strong dependence on time; it is also found that there were a significant uptake in the pancreas for an obvious CT imaging. And the following investigations showed that the raw CdS could damage the tissues accumulating nanoparticles. Through this work, it can be seen that the raw CdS being modified might be an excellent photographic developer for detecting cancers or other diseases.

  1. The synthesis of cadmium sulfide nanoplatelets using a novel continuous flow sonochemical reactor

    SciTech Connect

    Palanisamy, Barath; Paul, Brian; Chang, Chih -hung

    2015-01-21

    A continuous flow sonochemical reactor was developed capable of producing metastable cadmium sulfide (CdS) nanoplatelets with thicknesses at or below 10 nm. The continuous flow sonochemical reactor included the passive in-line micromixing of reagents prior to sonochemical reaction. Synthesis results were compared with those from reactors involving batch conventional heating and batch ultrasound-induced heating. The continuous sonochemical synthesis was found to result in high aspect ratio hexagonal platelets of CdS possessing cubic crystal structures with thicknesses well below 10 nm. The unique shape and crystal structure of the nanoplatelets are suggestive of high localized temperatures within the sonochemical process. As a result, the particle size uniformity and product throughput are much higher for the continuous sonochemical process in comparison to the batch sonochemical process and conventional synthesis processes.

  2. Chemical bath deposition of cadmium sulfide on graphene-coated flexible glass substrate

    SciTech Connect

    Seo, Won-Oh; Jung, Younghun; Kim, Jihyun; Kim, Jiwan; Kim, Donghwan

    2014-03-31

    We demonstrate a flexible structure of cadmium sulfide (CdS) on graphene-coated glass substrate, where CdS was deposited by the chemical bath deposition method on defective tri-layer graphene. The defects in graphene, confirmed by micro-Raman spectroscopy, were created by a ultra-violet treatment with varying exposure time from 10 to 60 min. The number of defect sites in the graphene as a seed layer was related to the quality of the CdS thin films determined from the results from X-ray diffraction, optical transmittance, scanning electron microscopy, and room temperature micro-photoluminescence. Our film-on-substrate structure of CdS-graphene-on-glass was maintained up to a tensile strain of 0.3%, where graphene with a high failure strain was employed as a transparent conductive layer.

  3. Genotoxicity and Cytotoxicity of Cadmium Sulfide Nanomaterials to Mice: Comparison Between Nanorods and Nanodots

    PubMed Central

    Liu, Lu; Sun, Meiqing; Li, Qingzhao; Zhang, Hongmei; Alvarez, Pedro J.J.; Liu, Huajie; Chen, Wei

    2014-01-01

    Abstract Cadmium sulfide (CdS) nanomaterials (such as CdS nanodots or nanorods) are widely used in optical, electronic, and biological applications. Large-scale production and use of these materials will likely result in accidental and incidental releases, which raise concerns about their potential environmental and human-health impacts. Most studies on toxicity of Cd-containing nanomaterials have focused on nanodots, and the relative toxicity of Cd-containing nanorods is not well understood. Here, we compared genotoxicity and cytotoxicity of CdS nanorods (30–50 nm diameter, 500–1100 nm length) and cubic CdS nanodots (3–5 nm) in mice by examining total cadmium accumulation in organs, acute toxicity, DNA damage, spermatozoon viability and abnormality, kidney and liver damage, and oxidative stress. Compared with (smaller) nanodots, nanorods resulted in relatively low bioaccumulation, acute toxicity, and damage to spermatozoa and the tested organs. Differences in toxicity between CdS nanodots and nanorods could not be fully explained by differences in their metal ion (Cd2+) release patterns, based on control tests with mice gavaged with dissolved CdCl2 at equivalent concentrations. This underscores that toxicity of metallic nanomaterials could not be solely predicted based either on their elemental composition or on the amount of ions released before receptor intake. Particle morphology (including size) may also need to be considered. PMID:25053877

  4. Luminescent behavior of cadmium sulfide quantum dots for gallic acid estimation

    NASA Astrophysics Data System (ADS)

    Singh, Suman; Garg, Sourav; Chahal, Jitender; Raheja, Khushboo; Singh, Deepak; Singla, M. L.

    2013-03-01

    Thioglycolic acid capped cadmium sulfide (CdS/T) quantum dots have been synthesized using wet chemistry and their optical behavior has been investigated using UV-visible absorption and fluorescence spectroscopy. The role of the capping agent, sulfide source concentration, pH and temperature has been studied and discussed. Studies showed that alkaline pH leads to a decrease in the size of quantum dots and reflux temperature above 70 °C resulted in red-shift of emission spectra which is due to narrowing of the bandgap. Further, to reduce the toxicity and photochemical instability of quantum dots, the quantum dots have been functionalized with polyethylene glycol (PEG), which resulted in a 20% enhancement of the fluorescence intensity. The application potential of CdS/T-PEG quantum dots was further studied using gallic acid as a model compound. The sensing is based on fluorescence quenching of quantum dots in the presence of gallic acid, and this study showed linearity in the range from 1.3 × 10-8 to 46.5 × 10-8 mM, with a detection limit of 3.6 × 10-8 mM.

  5. Nitric oxide-activated hydrogen sulfide is essential for cadmium stress response in bermudagrass (Cynodon dactylon (L). Pers.).

    PubMed

    Shi, Haitao; Ye, Tiantian; Chan, Zhulong

    2014-01-01

    Nitric oxide (NO) and hydrogen sulfide (H2S) are important gaseous molecules, serving as important secondary messengers in plant response to various biotic and abiotic stresses. However, the interaction between NO and H2S in plant stress response was largely unclear. In this study, endogenous NO and H2S were evidently induced by cadmium stress treatment in bermudagrass, and exogenous applications of NO donor (sodium nitroprusside, SNP) or H2S donor (sodium hydrosulfide, NaHS) conferred improved cadmium stress tolerance. Additionally, SNP and NaHS treatments alleviated cadmium stress-triggered plant growth inhibition, cell damage and reactive oxygen species (ROS) burst, partly via modulating enzymatic and non-enzymatic antioxidants. Moreover, SNP and NaHS treatments also induced the productions of both NO and H2S in the presence of Cd. Interestingly, combined treatments with inhibitors and scavengers of NO and H2S under cadmium stress condition showed that NO signal could be blocked by both NO and H2S inhibitors and scavengers, while H2S signal was specifically blocked by H2S inhibitors and scavengers, indicating that NO-activated H2S was essential for cadmium stress response. Taken together, we assigned the protective roles of endogenous and exogenous NO and H2S in bermudagrass response to cadmium stress, and speculated that NO-activated H2S might be essential for cadmium stress response in bermudagrass.

  6. Effect of cadmium in sediments on colonization by benthic marine organisms: Role of interstitial cadmium and acid volatile sulfide in bioavailability

    SciTech Connect

    Hansen, D.; Berry, W.; Benyi, S.; Mahony, J.; Corbin, J.; Pratt, S.; Able, M.

    1995-12-31

    The role of interstitial cadmium and acid volatile sulfide (AVS) in controlling the bioavailability of sediment-associated metal was examined using the chronic saltwater benthic colonization test. Sediments were spiked with cadmium to achieve simultaneously extracted metal (SEM)/AVS molar ratios of 0. 0 (control), 0.1, 0.8 and 3.0 in this 118-day test. Oxidation of AVS in the surficial 2.4 cm within two to four weeks resulted in sulfide profiles similar to those occurring naturally in local sediments. In the nominal 0.1 SEM/AVS treatment, measured SEM was always less than AVS. Interstitial cadmium concentrations (< 3--10 {micro}g/L) were below those likely to cause biological effects. No significant biological effects were detected. In the nominal 0.8 SEM/AVS treatment, measured SEM commonly exceeded AVS in the surficial 2.4 cm of sediment. Interstitial cadmium concentrations (24--157 {micro}g/L) were likely of toxicological significance to sensitive species. Shifts were observed in presence/absence of species, and there were fewer macrobenthic polychaetes (Mediomastus ambiseta, Strebloapio benedicti and Podarke obscura) and unidentified meiofaunal nematodes. In the nominal 3.0 SEM/AVS treatment, concentrations of SEM were always greater than AVS throughout the sediment column. Interstitial cadmium ranged from 28,000 to 174,000 {micro}g/L. In addition to the effects above, these sediments were colonized by fewer macrobenthic species, polychaete species and harpacticoids; had lower densities of diatoms; lacked bivalve molluscs and exhibited other impacts. The observed biological responses were consistent with measured SEM/AVS ratios in surficial sediments and interstitial water cadmium concentrations, further supporting their utility in predicting metals bioavailability.

  7. Characterization of cadmium telluride grain boundaries in cadmium telluride/cadmium sulfide solar cells

    NASA Astrophysics Data System (ADS)

    Woods, Lawrence Matthew

    2000-10-01

    During the May 18, 1980 eruption of Mount St. Helens the Muddy River, which drains 350 km2 on the east flank of the mountain, was inundated by lahars (volcanic debris flows). Channels and flood plains were stripped of vegetation and 0--2.5 meters of sediment were deposited. In addition, Smith Creek, a tributary of the Muddy River, was affected by the lateral blast which, in conjunction with lahars, deposited up to 15 m of sediment. The U.S. Geological Survey conducted repeat cross section surveys at least annually on 25 monumented cross sections in the study area from 1980 to 1986 and from 1994 to 1996. Channel adjustments were rapid and large; up to 12 m of incision and 8 m of aggradation within two years on Smith Creek and 3.5 m of incision on the Muddy River. Suspended sediment yields were high, 3,790,000 tons in 1982, with channel scour an important contributor. This study examined controls on the magnitude and timing of thalweg elevation and net cross section area changes. Two hypotheses were tested: (1) valley morphology is correlated to the timing and magnitude of channel adjustment, (2) channel adjustments occurred through complex response or the movement of a sediment wave. Four multiple linear regression models were run for each of the channel adjustment variables. The disturbance on Smith Creek by the blast deposition was great the minority carriers before the grain boundary, and reduce minority-carrier recombination. It was also shown that the Nitric-Phosphoric (NP) etching reduces the grain-boundary barrier heights to a value that correlates with the valence-band offsets between CdTe and Te. This effect of the NP-etch on grain boundaries extends down a minimum of 2.5 mum from the etched back contact surface. The effects of the NP-etch are also shown to be unstable and could translate to severe increases in the back-contact series resistance of devices. Finally, it was shown that there was no significant effect of the CdTe source plate usage on the inplane electrical properties, and that there is no indication of any grain-boundary barrier height inhomogeneity in any of the samples.

  8. Surface modification of cadmium sulfide thin film honey comb nanostructures: Effect of in situ tin doping using chemical bath deposition

    NASA Astrophysics Data System (ADS)

    Wilson, K. C.; Basheer Ahamed, M.

    2016-01-01

    Even though nanostructures possess large surface to volume ratio compared to their thin film counterpart, the complicated procedure that demands for the deposition on a substrate kept them back foot in device fabrication techniques. In this work, a honey comb like cadmium sulfide (CdS) thin films nanostructure are deposited on glass substrates using simple chemical bath deposition technique at 65 °C. Energy band gaps, film thickness and shell size of the honey comb nanostructures are successfully controlled using tin (Sn) doping and number of shells per unit area is found to be maximum for 5% Sn doped (in the reaction mixture) sample. X-ray diffraction and optical absorption analysis showed that cadmium sulfide and cadmium hydroxide coexist in the samples. TEM measurements showed that CdS nanostructures are embedded in cadmium hydroxide just like "plum pudding". Persistent photoconductivity measurements of the samples are also carried out. The decay constants found to be increased with increases in Sn doping.

  9. Cadmium solubility in paddy soils: effects of soil oxidation, metal sulfides and competitive ions.

    PubMed

    de Livera, Jennifer; McLaughlin, Mike J; Hettiarachchi, Ganga M; Kirby, Jason K; Beak, Douglas G

    2011-03-15

    Cadmium (Cd) is a non-essential element for human nutrition and is an agricultural soil contaminant. Cadmium solubility in paddy soils affects Cd accumulation in the grain of rice. This is a human health risk, exacerbated by the fact that rice grains are deficient in iron (Fe) and zinc (Zn) for human nutrition. To find ways of limiting this potential risk, we investigated factors influencing Cd solubility relative to Fe and Zn during pre-harvest drainage of paddy soils, in which soil oxidation is accompanied by the grain-filling stage of rice growth. This was simulated in temperature-controlled "reaction cell" experiments by first excluding oxygen to incubate soil suspensions anaerobically, then inducing aerobic conditions. In treatments without sulfur addition, the ratios of Cd:Fe and Cd:Zn in solution increased during the aerobic phase while Cd concentrations were unaffected and the Fe and Zn concentrations decreased. However, in treatments with added sulfur (as sulfate), up to 34 % of sulfur (S) was precipitated as sulfide minerals during the anaerobic phase and the Cd:Fe and Cd:Zn ratios in solution during the aerobic phase were lower than for treatments without S addition. When S was added, Cd solubility decreased whereas Fe and Zn were unaffected. When soil was spiked with Zn the Cd:Zn ratio was lower in solution during the aerobic phase, due to higher Zn concentrations. Decreased Cd:Fe and Cd:Zn ratios during the grain filling stage could potentially limit Cd enrichment in paddy rice grain due to competitive ion effects for root uptake.

  10. Indium phosphide/cadmium sulfide thin-film solar cells

    SciTech Connect

    Zanio, K.

    1980-02-01

    Thin-film InP/CdS structures were prepared by depositing, in sequence, ITO on a low-cost glass substrate, CdS on the ITO by thermal evaporation, and InP on the CdS by planar reactive deposition (PRD). Films of CdS, 15 ..mu..m thick, were recrystallized in flowing H/sub 2//H/sub 2/S at 500/sup 0/C. Lateral dimensions of typical grains were 50..mu..m with values up to 200 ..mu..m. The sheet resistance of the recrystallized CdS (RXCdS) was lowered from greater than 10/sup 5/ ..cap omega../O = cm/sup 2/ to values as low as 16 ..cap omega../O = cm/sup 2/ by annealing in either H/sub 2/ Cd atmospheres. Epitaxy of InP was undertaken on (100) InP at a substrate temperature of 320/sup 0/C. Room-temperature electron mobilities of about 2000 cm/sup 2//V-sec were found. Mobilities and hole concentrations of 60 cm/sup 2//V-sec and 10/sup 17/ cm-/sup 3/, respectively, were achieved with Be-doped films. P-type films with hole concentrations as high as a few times 10/sup 18/cm-/sup 3/ were achieved with increased doping. Be-doped InP was deposited onto the RXCdS/ITO/GLASS substrate to form a thin-film cell. However, p-type InP could not be prepared with CdS as a substrat4e, presumably due to interdiffusion or vapor transport of sulfur. Consequently, blocking action and a photovoltage could only be achieved using a gold Schottky barrier on the InP/RXCdS/ITO/GLASS structure. Plans for the next quarter include determining whether n-type doping from the CdS occurs by either interdiffusion or vapor transport, characterizing InP epitaxy on the RXCdS, and preparing additional thin-film structures.

  11. Engineering of nanocrystalline cadmium sulfide thin films by using swift heavy ions

    NASA Astrophysics Data System (ADS)

    Ahire, R. R.; Sagade, Abhay A.; Deshpande, N. G.; Chavhan, S. D.; Sharma, Ramphal; Singh, F.

    2007-08-01

    Swift heavy ion (SHI) irradiation experiments have been performed on as-deposited nanocrystalline cadmium sulfide (CdS) thin films by using 100 MeV Au8+ ions with 5 × 1012 ions cm-2. In addition, the as-deposited films were annealed at 300 °C in air for 1 h. Structural, optical and electrical properties of pristine (as-deposited), annealed and irradiated thin films were carried out by using x-ray diffraction (XRD), energy dispersive spectra, scanning electron microscopy, atomic force microscopy, UV-VIS spectroscopy and Arrhenius plots for resistivity and thermoemf, respectively. XRD shows the intrinsic peak of (0 0 2) for the hexagonal phase of CdS. After annealing and SHI irradiation this peak was enhanced drastically and dramatically, showing the dominant orientation in this plane. The grain growth observed in these two post-deposition processes was different. This resulted in a decrease in resistivity of the annealed and the irradiated samples by one and two orders from the pristine sample, respectively.

  12. An amperometric chloramphenicol immunosensor based on cadmium sulfide nanoparticles modified-dendrimer bonded conducting polymer.

    PubMed

    Kim, Dong-Min; Rahman, Md Aminur; Do, Minh Hien; Ban, Changill; Shim, Yoon-Bo

    2010-03-15

    An amperometric chloramphenicol (CAP) immunosensor was fabricated by covalently immobilizing anti-chloramphenicol acetyl transferase (anti-CAT) antibody on cadmium sulfide nanoparticles (CdS) modified-dendrimer that was bonded to the conducting polymer (poly 5, 2': 5', 2''-terthiophene-3'-carboxyl acid (poly-TTCA)) layer. The AuNPs, dendrimers, and CdS nanoparticles were deposited onto the polymer layer in order to enhance the sensitivity of the sensor probes. The particle sizes were determined using scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The immobilization of dendrimers, CdS, and anti-CAT were confirmed using energy disruptive spectroscopy (EDS), X-ray photoelectron spectroscopy (XPS), and quartz crystal microbalance (QCM) techniques. The detection of CAP was based on the competitive immuno-interaction between the free- and labeled-CAP for active sites of the anti-CAT. Hydrazine was used as the label for CAP, and it electrochemically catalyzed the reduction of H(2)O(2) at -0.35 V vs. Ag/AgCl. Under optimized conditions, the proposed immunosensor exhibited a linear range of CAP detection between 50 pg/mL and 950 pg/mL, and the detection limit was 45 pg/mL. The immunosensor was examined in real meat samples for the analysis of CAP.

  13. Direct electrochemical stripping detection of cystic-fibrosis-related DNA linked through cadmium sulfide quantum dots

    NASA Astrophysics Data System (ADS)

    Marin, Sergio; Merkoçi, Arben

    2009-02-01

    Electrochemical detection of a cadmium sulfide quantum dots (CdS QDs)-DNA complex connected to paramagnetic microbeads (MB) was performed without the need for chemical dissolving. The method is based on dropping 20 µl of CdS QD-DNA-MB suspension on the surface of a screen-printed electrode. It is followed by magnetic collection on the surface of the working electrode and electrochemical detection using square-wave voltammetry (SWV), giving a well-shaped and sensitive analytical signal. A cystic-fibrosis-related DNA sequence was sandwiched between the two DNA probes. One DNA probe is linked via biotin-streptavidin bonding with MB and the other one via thiol groups with the CdS QD used as tags. Nonspecific signals of DNA were minimized using a blocking agent and the results obtained were successfully employed in a model DNA sensor with an interest in future applications in the clinical field. The developed nanoparticle biosensing system may offer numerous opportunities in other fields where fast, low cost and efficient detection of small volume samples is required.

  14. A facile synthesis of novel nanorod-assembling hollow nanowires of cadmium sulfide/DBTU nanocomposite

    SciTech Connect

    Tang, Yu; Mo, Yan-mei; Yang, Kui; Chen, Tie-shi; Yang, Jun; Zhang, Yuan-ming

    2010-11-15

    Novel nanorod-assembling hollow nanowires of cadmium sulfide/DBTU (N,N'-dibutylthiourea) nanocomposite were synthesized by reacting CdCl{sub 2} with in situ produced H{sub 2}S from reaction of butylamine and carbon disulfide at molar ratio 3:3 of CS{sub 2}:BuNH{sub 2} at 50 {sup o}C. This product was characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM), selected area electron diffraction (SEAD), energy dispersive X-ray spectroscopy (EDAX), thermogravimetric (TG), Fourier transform infrared (FTIR) and UV-vis absorption spectra. A plausible mechanism that the extending DBTU molecules in solvent of CS{sub 2} induce the formation of CdS/DBTU nanorods by coordinating with the formed CdS particles, and construct these nanorods to hollow nanowires via molecular interactions is proposed and discussed on the basis of experimental results. Photoluminescence (PL) of CdS/DBTU nanocomposite exhibits increasing emission intensity largely.

  15. Synthesis, structural and optical properties of Sm{sup 3+} and Nd{sup 3+} doped cadmium sulfide nanocrystals

    SciTech Connect

    L, Saravanan; R, Jayavel; A, Pandurangan; Jih-Hsin, Liu; Hsin-Yuan, Miao

    2014-04-01

    Graphical abstract: Samarium (Sm{sup 3+}) and neodymium (Nd{sup 3+}) doped cadmium sulfide nanocrystals have been prepared via precipitation method. The structural and the luminescent properties of the as-synthesised nanocrystals have been discussed. - Highlights: • Cubic phase lanthanide ion doped cadmium sulfide nanocrystals were prepared by co-precipitation method. • HRTEM displays randomly aggregated nanoparticles with well-defined lattice fringes. • Energy gap and optical properties were affected by the different doping ions. • Effect of Sm and Nd ion doping on photo-emission of CdS nanocrystals was clarified. - Abstract: Cubic phase samarium (Sm{sup 3+}) and neodymium (Nd{sup 3+}) doped cadmium sulfide nanocrystals were synthesized through the chemical co-precipitation method. The crystallite size computed with high intense (1 1 1) peak using Scherrer formula was ∼3 nm. Morphology was examined with scanning electron microscopy (SEM). The transmission electron microscopy (TEM) images further established the formation of nanoclusters and EDAX spectra confirms the presence of cadmium, sulphide and rare earth elements in the sample. SAED pattern shows the crystallinity of the synthesized sample. Blue shift in the bandgap energy in the reflectance UV spectra, illustrates size quantization effect and dopant ion incorporation into the host lattice. The effect of doping concentrations of Sm{sup 3+} and Nd{sup 3+} on the luminescence spectra of CdS was studied. The emission spectra revealed that the intensity increased considerably in the presence of dopant ions. The variation in the optical properties and the enhancement in the luminescence were discussed for different doping levels.

  16. Cadmium Telluride Solar Cells with PEDOT:PSS Back Contact

    NASA Astrophysics Data System (ADS)

    Mount, Michael; Duarte, Fernanda; Paudel, Naba; Yan, Yanfa; Wang, Weining

    Cadmium Telluride (CdTe) solar cell is one of the most promising thin film solar cells and its highest efficiency has reached 21%. To keep improving the efficiency of CdTe solar cells, a few issues need to be addressed, one of which is the back contact. The back contact of CdTe solar cells are mostly Cu-base, and the problem with Cu-based back contact is that Cu diffuses into the grain boundary and into the CdS/CdTe junction, causing degradation problem at high temperature and under illumination. To continue improving the efficiency of CdTe/CdS solar cells, a good ohmic back contact with high work function and long term stability is needed. In this work, we report our studies on the potential of conducting polymer being used as the back contact of CdTe/CdS solar cells. Conducting polymers are good candidates because they have high work functions and high conductivities, are easy to process, and cost less, meeting all the requirements of a good ohmic back contact for CdTe. In our studies, we used poly(3,4-ethylenedioxythiophene) polystyrene sulfonate (PEDOT:PSS) with different conductivities and compared them with traditional Cu-based back contact. It was observed that the CdTe solar cell performance improves as the conductivity of the PEDOT:PSS increase, and the efficiency (9.1%) is approaching those with traditional Cu/Au back contact (12.5%). Cadmium Telluride Solar Cells with PEDOT:PSS Back Contact.

  17. Electrodeposited cobalt sulfide hole collecting layer for polymer solar cells

    SciTech Connect

    Zampetti, Andrea; De Rossi, Francesca; Brunetti, Francesca; Reale, Andrea; Di Carlo, Aldo; Brown, Thomas M.

    2014-08-11

    In polymer solar cells based on the blend of regioregular poly(3-hexylthiophene) (P3HT) and phenyl-C61-butyric acid methyl ester, the hole collecting layer has to be endowed with its ionization potential close to or greater than that of P3HT (∼5 eV). Conductive polymer blends such as poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) and metal oxides such as vanadium pentoxide (V{sub 2}O{sub 5}) and molybdenum trioxide (MoO{sub 3}) satisfy this requirement and have been the most common materials used so far in bulk heterojunction structures. We report here cobalt sulfide (CoS) to be a promising hole collecting material deposited by convenient and room temperature electrodeposition. By simply tuning the CoS electrodeposition parameters, power conversion efficiencies similar (within 15%) to a reference structure with PEDOT:PSS were obtained.

  18. Hydrogen sulfide alleviates cadmium-induced morpho-physiological and ultrastructural changes in Brassica napus.

    PubMed

    Ali, Basharat; Gill, Rafaqat A; Yang, Su; Gill, Muhammad B; Ali, Shafaqat; Rafiq, Muhammad T; Zhou, Weijun

    2014-12-01

    In the present study, role of hydrogen sulfide (H2S) in alleviating cadmium (Cd) induced stress in oilseed rape (Brassica napus L.) was studied under greenhouse conditions. Plants were grown hydroponically under three levels (0, 100, and 500µM) of Cd and three levels (0, 100 and 200µM) of H2S donor, sodium hydrosulfide (NaHS). Results showed that application of H2S significantly improved the plant growth, root morphology, chlorophyll contents, elements uptake and photosynthetic activity in B. napus plants under Cd stress. Moreover, addition of H2S reduced the Cd concentration in the leaves and roots of B. napus plants under Cd-toxicity. Exogenously applied H2S decreased the production of malondialdehyde and reactive oxygen species in the leaves and roots by improving the enzymatic antioxidant activities under Cd stress conditions. The microscopic examination indicated that application of exogenous H2S improved the cell structures and enabled a clean mesophyll cell having a well developed chloroplast with thylakoid membranes, and a number of mitochondria could be observed in the micrographs. A number of modifications could be found in root tip cell i.e. mature mitochondria, long endoplasmic reticulum and golgibodies under combined application of H2S and Cd. On the basis of these findings, it can be concluded that application of exogenous H2S has a protective role on plant growth, photosynthetic parameters, elements uptake, antioxidants enzyme activities and ultrastructural changes in B. napus under high Cd stress conditions.

  19. Cadmium sulfide quantum dots stabilized by castor oil and ricinoleic acid

    NASA Astrophysics Data System (ADS)

    Kyobe, Joseph William; Mubofu, Egid Beatus; Makame, Yahya M. M.; Mlowe, Sixberth; Revaprasadu, Neerish

    2016-02-01

    Castor oil and ricinoleic acid (an isolate of castor oil) are environmentally friendly bio-based organic surfactants that have been used as capping agents to prepare nearly spherical cadmium sulfide quantum dots (QDs) at 230, 250 and 280 °C. The prepared quantum dots were characterized by Ultra violet-visible (UV-vis), Photoluminescence (PL), Transmission Electron Microscopy (TEM), High Resolution Transmission Electron Microscopy (HRTEM) and X-ray diffraction (XRD) giving an overall CdS QDs average size of 5.14±0.39 nm. The broad XRD pattern and crystal lattice fringes in the HRTEM images showed a hexagonal phase composition of the CdS QDs. The calculated/estimated average size of the prepared castor oil capped CdS QDs for various techniques were 4.64 nm (TEM), 4.65 nm (EMA), 5.35 nm (UV-vis) and 6.46 nm (XRD). For ricinoleic acid capped CdS QDs, the average sizes were 5.56 nm (TEM), 4.78 nm (EMA), 5.52 nm (UV-vis) and 8.21 nm (XRD). Optical properties of CdS QDs showed a change of band gap energy from its bulk band gap of 2.42-2.82 eV due to quantum size confinement effect for temperature range of 230-280 °C. Similarly, a blue shift was observed in the photoluminescence spectra. Scanning electron microscope (SEM) observations show that the as-synthesized CdS QDs structures are spherical in shape. Fourier transform infra-red (FTIR) studies confirms the formation of castor oil and ricinoleic acid capped CdS QDs.

  20. Effects of different annealing atmospheres on the properties of cadmium sulfide thin films

    SciTech Connect

    Yücel, E.; Kahraman, S.; Güder, H.S.

    2015-08-15

    Graphical abstract: The effects of different annealing atmospheres (air and sulfur) on the structural, morphological and optical properties of CdS thin films were studied at three different pH values. - Highlights: • Compactness and smoothness of the films were enhanced after sulfur annealing. • Micro-strain values of some films were improved after sulfur annealing. • Dislocation density values of some films were improved after sulfur annealing. • Band gap values of the films were improved after sulfur annealing. - Abstract: Cadmium sulfide (CdS) thin films were prepared on glass substrates by using chemical bath deposition (CBD) technique. The effects of different annealing atmospheres (air and sulfur) on the structural, morphological and optical properties of CdS thin films were studied at three different pH values. Compactness and smoothness of the films (especially for pH 10.5 and 11) enhanced after sulfur annealing. pH value of the precursor solution remarkably affected the roughness, uniformity and particle sizes of the films. Based on the analysis of X-ray diffraction (XRD) patterns of the films, micro-strain and dislocation density values of the sulfur-annealed films (pH 10.5 and 11) were found to be lower than those of air-annealed films. Air-annealed films (pH 10.5, 11 and 11.5) exhibited higher transmittance than sulfur-annealed films in the wavelength region of 550–800 nm. Optical band gap values of the films were found between 2.31 eV and 2.36 eV.

  1. Polycrystalline thin film cadmium telluride solar cells fabricated by electrodeposition

    NASA Astrophysics Data System (ADS)

    Trefny, J. U.; Furtak, T. E.; Williamson, D. L.; Kim, D.

    1994-07-01

    This report describes the principal results of work performed during the second year of a 3-year program at the Colorado School of Mines (CSM). The work on transparent conducting oxides was carried out primarily by CSM students at NREL and is described in three publications listed in Appendix C. The high-quality ZnO produced from the work was incorporated into a copper indium diselenide cell that exhibited a world-record efficiency of 16.4%. Much of the time was devoted to the improvement of cadmium sulfide films deposited by chemical bath deposition methods and annealed with or without a cadmium chloride treatment. Progress was also made in the electrochemical deposition of cadmium telluride. High-quality films yielding CdS/CdTe/Au cells of greater than 10% efficiency are now being produced on a regular basis. We explored the use of zinc telluride back contacts to form an n-i-p cell structure as previously used by Ametek. We began small-angle x-ray scattering (SAXS) studies to characterize crystal structures, residual stresses, and microstructures of both CdTe and CdS. Large SAXS signals were observed in CdS, most likely because of scattering from gain boundaries. The signals observed to date from CdTe are much weaker, indicating a more homogeneous microstructure. We began to use the ADEPT modeling program, developed at Purdue University, to guide our understanding of the CdS/CdTe cell physics and the improvements that will most likely lead to significantly enhanced efficiencies.

  2. Thin-film cadmium telluride solar cells

    NASA Astrophysics Data System (ADS)

    Chu, T. L.

    1986-08-01

    The major objective of this work was to demonstrate CdTe devices grown by chemical vapor deposition (CVD) with a total area greater than 1 cm2 and photovoltic efficiencies of at least 13%. During the period covered, various processing steps were investigated for the preparation of thin-film CdTe heterojunction solar cells of the inverted configuration. Glass coated with fluorine-doped tin oxide was used as the substrate. Thin-film heterojunction solar cells were prepared by depositing p-CdTe films on substrates using CVD and close-spaced sublimation (CSS). Cells prepared from CSS CdTe usually have a higher conversion efficiency than those prepared from CVD CdTe, presumably due to the chemical interaction between CdS and CdTe at the interface during the CVD process. The best cell, about 1.2 sq cm in area, had an AM 1.5 (global) efficiency of 10.5%, and further improvements are expected by optimizing the process parameters.

  3. Towards understanding junction degradation in cadmium telluride solar cells

    SciTech Connect

    Nardone, Marco

    2014-06-21

    A degradation mechanism in cadmium telluride (CdTe/CdS) solar cells is investigated using time-dependent numerical modeling to simulate various temperature, bias, and illumination stress conditions. The physical mechanism is based on defect generation rates that are proportional to nonequilibrium charge carrier concentrations. It is found that a commonly observed degradation mode for CdTe/CdS solar cells can be reproduced only if defects are allowed to form in a narrow region of the absorber layer close to the CdTe/CdS junction. A key aspect of this junction degradation is that both mid-gap donor and shallow acceptor-type defects must be generated simultaneously in response to photo-excitation or applied bias. The numerical approach employed here can be extended to study other mechanisms for any photovoltaic technology.

  4. Improving the efficiency of cadmium sulfide-sensitized titanium dioxide/indium tin oxide glass photoelectrodes using silver sulfide as an energy barrier layer and a light absorber

    PubMed Central

    2014-01-01

    Cadmium sulfide (CdS) and silver sulfide (Ag2S) nanocrystals are deposited on the titanium dioxide (TiO2) nanocrystalline film on indium tin oxide (ITO) substrate to prepare CdS/Ag2S/TiO2/ITO photoelectrodes through a new method known as the molecular precursor decomposition method. The Ag2S is interposed between the TiO2 nanocrystal film and CdS nanocrystals as an energy barrier layer and a light absorber. As a consequence, the energy conversion efficiency of the CdS/Ag2S/TiO2/ITO electrodes is significantly improved. Under AM 1.5 G sunlight irradiation, the maximum efficiency achieved for the CdS(4)/Ag2S/TiO2/ITO electrode is 3.46%, corresponding to an increase of about 150% as compared to the CdS(4)/TiO2/ITO electrode without the Ag2S layer. Our experimental results show that the improved efficiency is mainly due to the formation of Ag2S layer that may increase the light absorbance and reduce the recombination of photogenerated electrons with redox ions from the electrolyte. PMID:25411566

  5. Thin-film cadmium telluride and zinc phosphide solar cells

    NASA Astrophysics Data System (ADS)

    Chu, T. L.

    1981-06-01

    Major efforts during this quarter were directed to the deposition and characterization of zinc phosphide and cadmium telluride films and solar cells. The deposition of zinc phosphide films by the reaction of zinc and phosphine in a hydrogen atmosphere was continued and the composition of deposited films was determined. For more efficient utilization of phosphine, a 8500 C zone was added to the deposition. The in-situ annealing of zinc phosphide in phosphine was carried out. Attempts to prepare solar cell structures by depositing a thin film of zinc phosphide on an annealed film were made; however, the results are inconclusive. The deposition of cadmium telluride films by the direct combination of the elements under reduced pressure and under atmospheric pressure was carried out. Films deposited under reduced pressure exhibited more compact grain structures, however, they showed poor photoresponse. The composition of the films deposited under atmospheric pressure were analyzed and the dependence of short circuit density on the reactant composition was investigated.

  6. CADMIUM SOLUBILITY IN PADDY SOILS: EFFECTS OF SOIL OXIDATION, METAL SULFIDES AND COMPETITIVE IONS.

    EPA Science Inventory

    Cadmium (Cd) is a non-essential element for human nutrition and is an agricultural soil contaminant. Cadmium solubility in paddy soils affects Cd accumulation in the grain of rice. This is a human health risk, exacerbated by the fact that rice grains are deficient in iron (Fe) an...

  7. Flow-injection chemiluminescence analysis for sensitive determination of atenolol using cadmium sulfide quantum dots

    NASA Astrophysics Data System (ADS)

    Khataee, Alireza; Lotfi, Roya; Hasanzadeh, Aliyeh; Iranifam, Mortaza; Joo, Sang Woo

    2016-03-01

    A sensitive, rapid and simple flow-injection chemiluminescence (CL) system based on the light emitted from KMnO4-cadmium sulfide quantum dots (CdS QDs) reaction in the presence of cetyltrimethylammonium bromide (CTAB) in acidic medium was developed as a CL probe for the sensitive determination of atenolol. Optical and structural features of CdS QDs capped with L-cysteine, which synthesized via hydrothermal approach, were investigated using X-ray diffraction (XRD), scanning electron microscopy (SEM), photoluminescence (PL), and UV-Vis spectroscopy. The CL intensity of KMnO4-CdS QDs-CTAB was remarkably enhanced in the presence of trace level of atenolol. Under optimum experimental conditions, there is a linear relationship between the increase in CL intensity of KMnO4-CdS QDs-CTAB system and atenolol concentration in a range of 0.001 to 4.0 mg L- 1 and 4.0 to 18.0 mg L- 1, with a detection limit (3σ) of 0.0010 mg L- 1. A possible mechanism for KMnO4-CdS QDs-CTAB-atenolol CL reaction is proposed. To prove the practical application of the KMnO4-CdS QDs-CTAB CL method, the method was applied for the determination of atenolol in spiked environmental water samples and commercial pharmaceutical formulation. Furthermore, corona discharge ionization ion mobility spectrometry (CD-IMS) technique was utilized for determination of atenolol. Figure S2. Optimization of the CL reaction conditions: (a) effect of KMnO4 concentration. Conditions: the concentrations of H2SO4, CdS QDs and atenolol were 1 mol L-1, 0.35 mol L-1, and 4.0 mg L-1, respectively; (b) effect of acidic media. Conditions: the concentrations of KMnO4 was 0.04 mmol L-1, other conditions were as in (a); (c) effect of CdS QDs concentration. Conditions: H2SO4 concentration was 1.0 mol L-1, other conditions were as in (b), and (d) effect of CTAB concentration. Conditions: CdS QDs concentration was 0.35 mmol L-1, other conditions were as in (c). Figure S3. UV-Vis absorption spectra of KMnO4-CdS QDs-atenolol CL system

  8. Directionally asymmetric self-assembly of cadmium sulfide nanotubes using porous alumina nanoreactors: Need for chemohydrodynamic instability at the nanoscale

    NASA Astrophysics Data System (ADS)

    Varghese, Arthur; Datta, Shouvik

    2012-05-01

    We explore nanoscale hydrodynamical effects on synthesis and self-assembly of cadmium sulfide nanotubes oriented along one direction. These nanotubes are synthesized by horizontal capillary flow of two different chemical reagents from opposite directions through nanochannels of porous anodic alumina which are used primarily as nanoreactors. We show that uneven flow of different chemical precursors is responsible for directionally asymmetric growth of these nanotubes. On the basis of structural observations using scanning electron microscopy, we argue that chemohydrodynamic convective interfacial instability of multicomponent liquid-liquid reactive interface is necessary for sustained nucleation of these CdS nanotubes at the edges of these porous nanochannels over several hours. However, our estimates clearly suggest that classical hydrodynamics cannot account for the occurrence of such instabilities at these small length scales. Therefore, we present a case which necessitates further investigation and understanding of chemohydrodynamic fluid flow through nanoconfined channels in order to explain the occurrence of such interfacial instabilities at nanometer length scales.

  9. Directionally asymmetric self-assembly of cadmium sulfide nanotubes using porous alumina nanoreactors: need for chemohydrodynamic instability at the nanoscale.

    PubMed

    Varghese, Arthur; Datta, Shouvik

    2012-05-01

    We explore nanoscale hydrodynamical effects on synthesis and self-assembly of cadmium sulfide nanotubes oriented along one direction. These nanotubes are synthesized by horizontal capillary flow of two different chemical reagents from opposite directions through nanochannels of porous anodic alumina which are used primarily as nanoreactors. We show that uneven flow of different chemical precursors is responsible for directionally asymmetric growth of these nanotubes. On the basis of structural observations using scanning electron microscopy, we argue that chemohydrodynamic convective interfacial instability of multicomponent liquid-liquid reactive interface is necessary for sustained nucleation of these CdS nanotubes at the edges of these porous nanochannels over several hours. However, our estimates clearly suggest that classical hydrodynamics cannot account for the occurrence of such instabilities at these small length scales. Therefore, we present a case which necessitates further investigation and understanding of chemohydrodynamic fluid flow through nanoconfined channels in order to explain the occurrence of such interfacial instabilities at nanometer length scales.

  10. Photocatalytic Activities of Copper Doped Cadmium Sulfide Microspheres Prepared by a Facile Ultrasonic Spray-Pyrolysis Method.

    PubMed

    Su, Jinzhan; Zhang, Tao; Li, Yufeng; Chen, Yubin; Liu, Maochang

    2016-01-01

    Ultrasonic spray pyrolysis is a superior method for preparing and synthesizing spherical particles of metal oxide or sulfide semiconductors. Cadmium sulfide (CdS) photocatalysts with different sizes and doped-CdS with different dopants and doping levels have been synthesized to study their properties of photocatalytic hydrogen production from water. The CdS photocatalysts were characterized with scanning electron microscopy (SEM), X-ray fluorescence-spectrometry (XRF), UV-Vis absorption spectra and X-ray diffraction (XRD) to study their morphological and optical properties. The sizes of the prepared CdS particles were found to be proportional to the concentration of the metal nitrates in the solution. The CdS photocatalyst with smaller size showed a better photocatalytic activity. In addition, Cu doped CdS were also deposited and their photocatalytic activities were also investigated. Decreased bandgaps of CdS synthesized with this method were found and could be due to high density surface defects originated from Cd vacancies. Incorporating the Cu elements increased the bandgap by taking the position of Cd vacancies and reducing the surface defect states. The optimal Cu-doped level was found to be 0.5 mol % toward hydrogen evolution from aqueous media in the presence of sacrificial electron donors (Na₂S and Na₂SO₃) at a pH of 13.2. This study demonstrated that ultrasonic spray pyrolysis is a feasible approach for large-scale photocatalyst synthesis and corresponding doping modification. PMID:27314320

  11. Effects of Buffer Salt Concentration on the Dominated Deposition Mechanism and Optical Characteristics of Chemically Deposited Cadmium Sulfide Thin Films

    NASA Astrophysics Data System (ADS)

    Kakhaki, Z. Makhdoumi; Youzbashi, A.; Sangpour, P.; Kazemzadeh, A.; Naderi, N.; Bazargan, A. M.

    2016-02-01

    Effects of buffer salt concentration on the rate of deposition, dominated deposition mechanism and subsequently the structural, morphological, and optical properties of cadmium sulfide (CdS) thin films deposited by chemical bath deposition (CBD) on glass substrate were investigated. The precursors were chosen to be cadmium chloride (CdCl2) as the cadmium source, thiourea (CS(NH2)2) as the sulfur source, ammonium nitrate (NH4NO3) as the buffer salt and ammonia as the complexing agent and the pH controller. The influence of the NH4NO3 concentration on the structure, morphology, film uniformity, stoichiometry and optical properties of CdS thin films was also studied by X-ray diffractometer (XRD), field emission scanning electron microscope (FE-SEM), energy dispersive X-ray (EDX) spectroscope, uv-visible and photoluminescence (PL) spectroscopes. The XRD studies revealed that all the deposited films exhibited a (002)h/(111)c preferred orientation. The crystallite size was increased from 20nm to 30nm by the increase of concentration of NH4NO3 from 0.5M to 2.5M. The morphology of CdS thin films were agglomerated spherical particles consisted of smaller particles. The surface of thin films deposited at the NH4NO3 concentration of 0.5M was compact and smooth. The increase of the concentration of NH4NO3 decreased the packing density of the films. The optical band gap was in the range of 2.25-2.4eV, which was decreased by the decrement of packing density. The PL spectra showed two peaks centered at 400nm and 500nm which are attributed to violet and band-to-band emissions, respectively.

  12. Solar Photovoltaic Cells.

    ERIC Educational Resources Information Center

    Mickey, Charles D.

    1981-01-01

    Reviews information on solar radiation as an energy source. Discusses these topics: the key photovoltaic material; the bank theory of solids; conductors, semiconductors, and insulators; impurity semiconductors; solid-state photovoltaic cell operation; limitations on solar cell efficiency; silicon solar cells; cadmium sulfide/copper (I) sulfide…

  13. Incorporation of sulfide ions into the cadmium(II) thiolate cluster of Cicer arietinum metallothionein2.

    PubMed

    Wan, Xiaoqiong; Freisinger, Eva

    2013-01-18

    The plant metallothionein2 from Cicer arietinum (chickpea), cic-MT2, is known to coordinate five divalent metal ions such as Zn(II) or Cd(II), which are arranged in a single metal thiolate cluster. When the Zn(II) form of the protein is titrated with Cd(II) ions in the presence of sulfide ions, an increased Cd(II) binding capacity and concomitant incorporation of sulfide ions into the cluster are observed. The exact stoichiometry of this novel cluster, its spectroscopic properties, and the significantly increased pH stability are analyzed with different techniques, including UV and circular dichroism spectroscopy and colorimetric assays. Limited proteolytic digestion provides information about the spacial arrangement of the cluster within the protein. Increasing the Cd(II) scavenging properties of a metallothionein by additionally recruiting sulfide ions might be an economic and very efficient detoxification strategy for plants.

  14. Solar decomposition of cadmium oxide for hydrogen production. Final subcontract report

    SciTech Connect

    Schreiber, J. D.; Yudow, B. D.; Carty, R. H.; Whaley, T. P.; Pangborn, J. B.

    1981-11-01

    The reactor developed for this study performed satisfactorily in establishing the feasibility of cadmium oxide decomposition under the realistic conditions of the solar-furnace environment. The solar-furnace environment is very appropriate for the evaluation of design concepts. However, the solar furnace probably cannot give precise rate data. The flux is too nonuniform, so temperatures of reactant and corresponding reaction rates are also nonuniform. One of the most important results of this project was the recovery of samples from the quench heat exchanger that contained a surprisingly large amount of metallic cadmium. The fact that the sample taken from the quench heat exchanger was metallic in appearance and contained between 67% and 84% metallic cadmium would tend to indicate recombination of cadmium vapor and oxygen can be effectively prevented by the quenching operation. It would also tend to confirm recent studies that show cadmium oxide does not sublime appreciably. Determination of the decomposition rate of cadmium oxide was severely limited by fluctuating and nonuniform reactant temperatures and baseline drift in the oxygen sensor. However, the estimated rate based on a single run seemed to follow a typical solid decomposition rate pattern with an initial acceleratory period, followed by a longer deceleratory period. From a preliminary flowsheet analysis of the cadmium-cadmium oxide cycle, it was determined that at a cadmium oxide decomposition temperature of 1400/sup 0/C and a requirement of 0.2 V in the electrolyzer the efficiency was 41%, assuming total quenching of the cadmium oxide decomposition products. This efficiency could increase to a maximum of 59% if total recovery of the latent heats of vaporization and fusion of the decomposition products is possible.

  15. Cadmium-Induced Hydrogen Sulfide Synthesis Is Involved in Cadmium Tolerance in Medicago sativa by Reestablishment of Reduced (Homo)glutathione and Reactive Oxygen Species Homeostases

    PubMed Central

    Cui, Weiti; Chen, Huiping; Zhu, Kaikai; Jin, Qijiang; Xie, Yanjie; Cui, Jin; Xia, Yan; Zhang, Jing; Shen, Wenbiao

    2014-01-01

    Until now, physiological mechanisms and downstream targets responsible for the cadmium (Cd) tolerance mediated by endogenous hydrogen sulfide (H2S) have been elusive. To address this gap, a combination of pharmacological, histochemical, biochemical and molecular approaches was applied. The perturbation of reduced (homo)glutathione homeostasis and increased H2S production as well as the activation of two H2S-synthetic enzymes activities, including L-cysteine desulfhydrase (LCD) and D-cysteine desulfhydrase (DCD), in alfalfa seedling roots were early responses to the exposure of Cd. The application of H2S donor sodium hydrosulfide (NaHS), not only mimicked intracellular H2S production triggered by Cd, but also alleviated Cd toxicity in a H2S-dependent fashion. By contrast, the inhibition of H2S production caused by the application of its synthetic inhibitor blocked NaHS-induced Cd tolerance, and destroyed reduced (homo)glutathione and reactive oxygen species (ROS) homeostases. Above mentioned inhibitory responses were further rescued by exogenously applied glutathione (GSH). Meanwhile, NaHS responses were sensitive to a (homo)glutathione synthetic inhibitor, but reversed by the cotreatment with GSH. The possible involvement of cyclic AMP (cAMP) signaling in NaHS responses was also suggested. In summary, LCD/DCD-mediated H2S might be an important signaling molecule in the enhancement of Cd toxicity in alfalfa seedlings mainly by governing reduced (homo)glutathione and ROS homeostases. PMID:25275379

  16. Integration of Semiconducting Sulfides for Full-Spectrum Solar Energy Absorption and Efficient Charge Separation.

    PubMed

    Zhuang, Tao-Tao; Liu, Yan; Li, Yi; Zhao, Yuan; Wu, Liang; Jiang, Jun; Yu, Shu-Hong

    2016-05-23

    The full harvest of solar energy by semiconductors requires a material that simultaneously absorbs across the whole solar spectrum and collects photogenerated electrons and holes separately. The stepwise integration of three semiconducting sulfides, namely ZnS, CdS, and Cu2-x S, into a single nanocrystal, led to a unique ternary multi-node sheath ZnS-CdS-Cu2-x S heteronanorod for full-spectrum solar energy absorption. Localized surface plasmon resonance (LSPR) in the nonstoichiometric copper sulfide nanostructures enables effective NIR absorption. More significantly, the construction of pn heterojunctions between Cu2-x S and CdS leads to staggered gaps, as confirmed by first-principles simulations. This band alignment causes effective electron-hole separation in the ternary system and hence enables efficient solar energy conversion.

  17. Acartia tonsa eggs as a biomonitor to evaluate bioavailability/toxicity of persistent contaminants in anoxic/sulfidic conditions: The case of cadmium and nickel.

    PubMed

    Sei, Sandra; Invidia, Marion; Giannetto, Marco; Gorbi, Gessica

    2016-10-01

    The evaluation of toxicity due to persistent pollutants in anoxic aquatic environments has met with various problems, as most test organisms can not withstand oxygen lack and exposure to free sulfide. We evaluated the suitability of the eggs of the brackish copepod Acartia tonsa for bioassays in anoxic/sulfidic conditions: when exposed to deep hypoxia and free sulfide, the eggs become quiescent and are able to resume hatching after restoring normoxic conditions. Tests with cadmium and nickel were performed in normoxic and deeply hypoxic conditions and in anoxic water containing H2S or H2S+FeSO4 on an equimolar basis. Active and quiescent eggs showed equivalent sensitivity to the metals, both suffering significant reductions in hatching success at 89μM Cd and 17μM Ni. As expected on the basis of the SEM/AVS model, Cd toxicity was almost completely suppressed in presence of sulfides. Dissolved Cd concentration drastically dropped and hatching success was generally >80%, as against values <6% observed in sulfide-free water, indicating that the applied experimental procedure can simulate metal-sulfide interaction. Ni toxicity was only slightly reduced by the presence of sulfides. High dissolved Ni concentrations were detected and mean hatching percentages were ≤32%, suggesting that Ni bioavailability/toxicity was only partially controlled by excess reactive sulfides. The results suggest that A. tonsa eggs could be a useful biomonitor to evaluate toxicity due persistent contaminants in anoxic conditions and the role of sulfides in reducing metal bioavailability/toxicity. PMID:27235834

  18. Synthesis, characterization and toxicological evaluation of maltodextrin capped cadmium sulfide nanoparticles in human cell lines and chicken embryos

    PubMed Central

    2012-01-01

    Background Semiconductor Quantum dots (QDs) have become quite popular thanks to their properties and wide use in biological and biomedical studies. However, these same properties entail new challenges in understanding, predicting, and managing potential adverse health effects following exposure. Cadmium and selenium, which are the major components of the majority of quantum dots, are known to be acutely and chronically toxic to cells and organisms. Protecting the core of nanoparticles can, to some degree, control the toxicity related to cadmium and selenium leakage. Results This study successfully synthesized and characterized maltodextrin coated cadmium sulfide semiconductor nanoparticles. The results show that CdS-MD nanoparticles are cytotoxic and embryotoxic. CdS-MD nanoparticles in low concentrations (4.92 and 6.56 nM) lightly increased the number of HepG2 cell. A reduction in MDA-MB-231 cells was observed with concentrations higher than 4.92 nM in a dose response manner, while Caco-2 cells showed an important increase starting at 1.64 nM. CdS-MD nanoparticles induced cell death by apoptosis and necrosis in MDA-MD-231 cells starting at 8.20 nM concentrations in a dose response manner. The exposure of these cells to 11.48-14.76 nM of CdS-MD nanoparticles induced ROS production. The analysis of cell proliferation in MDA-MB-231 showed different effects. Low concentrations (1.64 nM) increased cell proliferation (6%) at 7 days (p < 0.05). However, higher concentrations (>4.92 nM) increased cell proliferation in a dose response manner (15-30%) at 7 days. Exposures of chicken embryos to CdS-MD nanoparticles resulted in a dose-dependent increase in anomalies that, starting at 9.84 nM, centered on the heart, central nervous system, placodes, neural tube and somites. No toxic alterations were observed with concentrations of < 3.28 nM, neither in cells nor chicken embryos. Conclusions Our results indicate that CdS-MD nanoparticles induce cell death and alter cell

  19. Hydrogen Sulfide Alleviates Cadmium-Induced Cell Death through Restraining ROS Accumulation in Roots of Brassica rapa L. ssp. pekinensis.

    PubMed

    Zhang, Liping; Pei, Yanxi; Wang, Hongjiao; Jin, Zhuping; Liu, Zhiqiang; Qiao, Zengjie; Fang, Huihui; Zhang, Yanjie

    2015-01-01

    Hydrogen sulfide (H2S) is a cell signal molecule produced endogenously and involved in regulation of tolerance to biotic and abiotic stress in plants. In this work, we used molecular biology, physiology, and histochemical methods to investigate the effects of H2S on cadmium- (Cd-) induced cell death in Chinese cabbage roots. Cd stress stimulated a rapid increase of endogenous H2S in roots. Additionally, root length was closely related to the cell death rate. Pretreatment with sodium hydrosulfide (NaHS), a H2S donor, alleviated the growth inhibition caused by Cd in roots-this effect was more pronounced at 5 μM NaHS. Cd-induced cell death in roots was significantly reduced by 5 μM NaHS treatment. Under Cd stress, activities of the antioxidant enzymes were significantly enhanced in roots. NaHS + Cd treatment made their activities increase further compared with Cd exposure alone. Enhanced antioxidant enzyme activity led to a decline in reactive oxygen species accumulation and lipid peroxidation. In contrast, these effects were reversed by hydroxylamine, a H2S inhibitor. These results suggested that H2S alleviated the cell death caused by Cd via upregulation of antioxidant enzyme activities to remove excessive reactive oxygen species and reduce cell oxidative damage.

  20. The Proteomic Response of Arabidopsis thaliana to Cadmium Sulfide Quantum Dots, and Its Correlation with the Transcriptomic Response

    PubMed Central

    Marmiroli, Marta; Imperiale, Davide; Pagano, Luca; Villani, Marco; Zappettini, Andrea; Marmiroli, Nelson

    2015-01-01

    A fuller understanding of the interaction between plants and engineered nanomaterials is of topical relevance because the latter are beginning to find applications in agriculture and the food industry. There is a growing need to establish objective safety criteria for their use. The recognition of two independent Arabidopsis thaliana mutants displaying a greater level of tolerance than the wild type plant to exposure to cadmium sulfide quantum dots (CdS QDs) has offered the opportunity to characterize the tolerance response at the physiological, transcriptomic, and proteomic levels. Here, a proteomics-based comparison confirmed the conclusions drawn from an earlier transcriptomic analysis that the two mutants responded to CdS QD exposure differently both to the wild type and to each other. Just over half of the proteomic changes mirrored documented changes at the level of gene transcription, but a substantial number of transcript/gene product pairs were altered in the opposite direction. An interpretation of the discrepancies is given, along with some considerations regarding the use and significance of -omics when monitoring the potential toxicity of ENMs for health and environment. PMID:26732871

  1. Effect of different sulfides on cadmium distribution during sludge combustion based on experimental and thermodynamic calculation approaches.

    PubMed

    Liu, Jing-Yong; Fu, Jie-Wen; Sun, Shui-Yu; Ning, Xun-An; Wang, Yu-Jie; Chen, Tao; Luo, Guang-Qian; Xie, Wu-Ming; Yang, Zuo-Yi; Zhuo, Zhong-Xu

    2015-01-01

    The effects of sulfur compounds on the migration of a semi-volatile heavy metal (cadmium) during sludge incineration were investigated with two methods, i.e., experiments in a tubular furnace reactor and thermodynamic equilibrium calculations. The representative typical sludge with and without the addition of sulfur compounds was incinerated at 850 °C. The partitioning of Cd among the solid phase (bottom ash) and gas phase (fly ash and flue gas) was quantified. The results indicate that sulfur compounds in the elemental form and a reduced state could stabilize Cd in the form of CdS, aluminosilicate minerals, and polymetallic sulfides, whereas sulfur in the oxidized forms slightly increases Cd volatilization during incineration. For Cd solidification points, the inhibition effect on the volatilization of Cd is as follows: S > Na2SO4 > Na2S. Chemical equilibrium calculations indicate that sulfur binds with Cd and alters Cd speciation at low temperatures (<950 K). Furthermore, SiO2- and Al2O3-containing minerals can function as sorbents stabilizing Cd as condensed phase solids (CdSiO4 and CdAl2O4) according to the results of equilibrium calculations. These findings provide useful information for understanding the partitioning of Cd and thus facilitate the development of strategies to control Cd volatilization during sludge incineration.

  2. Hydrogen Sulfide Alleviates Cadmium-Induced Cell Death through Restraining ROS Accumulation in Roots of Brassica rapa L. ssp. pekinensis

    PubMed Central

    2015-01-01

    Hydrogen sulfide (H2S) is a cell signal molecule produced endogenously and involved in regulation of tolerance to biotic and abiotic stress in plants. In this work, we used molecular biology, physiology, and histochemical methods to investigate the effects of H2S on cadmium- (Cd-) induced cell death in Chinese cabbage roots. Cd stress stimulated a rapid increase of endogenous H2S in roots. Additionally, root length was closely related to the cell death rate. Pretreatment with sodium hydrosulfide (NaHS), a H2S donor, alleviated the growth inhibition caused by Cd in roots—this effect was more pronounced at 5 μM NaHS. Cd-induced cell death in roots was significantly reduced by 5 μM NaHS treatment. Under Cd stress, activities of the antioxidant enzymes were significantly enhanced in roots. NaHS + Cd treatment made their activities increase further compared with Cd exposure alone. Enhanced antioxidant enzyme activity led to a decline in reactive oxygen species accumulation and lipid peroxidation. In contrast, these effects were reversed by hydroxylamine, a H2S inhibitor. These results suggested that H2S alleviated the cell death caused by Cd via upregulation of antioxidant enzyme activities to remove excessive reactive oxygen species and reduce cell oxidative damage. PMID:26078819

  3. A circular dichroism sensor for Ni(2+) and Co(2+) based on L-cysteine capped cadmium sulfide quantum dots.

    PubMed

    Tedsana, Wimonsiri; Tuntulani, Thawatchai; Ngeontae, Wittaya

    2015-03-31

    A new circular dichroism sensor for detecting Ni(2+) and Co(2+) was proposed for the first time using chiral chelating quantum dots. The detection principle was based on changing of circular dichroism signals of the chiral quantum dots when forming a chiral complex with Ni(2+) or Co(2+). L-Cysteine capped cadmium sulfide quantum dots (L-Cyst-CdS QDs) were proposed as a chiral probe. The CD spectrum of L-Cyst-CdS QDs was significantly changed in the presence of Ni(2+) and Co(2+). On the other hand, other studied cations did not alter the original CD spectrum. Moreover, when increasing the concentration of Ni(2+) or Co(2+), the intensity of the CD spectrum linearly increased as a function of concentration and could be useful for the quantitative analysis. The proposed CD sensor showed linear working concentration ranges of 10-60 μM and 4-80 μM with low detection limits of 7.33 μМ and 1.13 μM for the detection of Ni(2+) and Co(2+), respectively. Parameters possibly affected the detection sensitivity such as solution pH and incubation time were studied and optimized. The proposed sensor was applied to detect Ni(2+) and Co(2+) in real water samples, and the results agreed well with the analysis using the standard ICP-OES.

  4. Size-controlled one-pot synthesis of fluorescent cadmium sulfide semiconductor nanoparticles in an apoferritin cavity.

    PubMed

    Iwahori, K; Yamashita, I

    2008-12-10

    A simple size-controlled synthesis of cadmium sulfide (CdS) nanoparticle (NP) cores in the cavity of apoferritin from horse spleen (HsAFr) was performed by a slow chemical reaction synthesis and a two-step synthesis protocol. We found that the CdS NP core synthesis was slow and that premature CdS NP cores were formed in the apoferritin cavity when the concentration of ammonia water was low. It was proven that the control of the ammonia water concentration can govern the CdS NP core synthesis and successfully produce size-controlled CdS NP cores with diameters from 4.7 to 7.1 nm with narrow size dispersion. X-ray powder diffraction (XRD), energy dispersive spectroscopy (EDS) analysis and high-resolution transmission electron microscopy (HR-TEM) observation characterized the CdS NP cores obtained as cubic polycrystalline NPs, which showed photoluminescence with red shifts depending on their diameters. From the research of CdS NP core synthesis in the recombinant apoferritins, the zeta potential of apoferritin is important for the biomineralization of CdS NP cores in the apoferritin cavity. These synthesized CdS NPs with different photoluminescence properties will be applicable in a wide variety of nano-applications.

  5. A circular dichroism sensor for Ni(2+) and Co(2+) based on L-cysteine capped cadmium sulfide quantum dots.

    PubMed

    Tedsana, Wimonsiri; Tuntulani, Thawatchai; Ngeontae, Wittaya

    2015-03-31

    A new circular dichroism sensor for detecting Ni(2+) and Co(2+) was proposed for the first time using chiral chelating quantum dots. The detection principle was based on changing of circular dichroism signals of the chiral quantum dots when forming a chiral complex with Ni(2+) or Co(2+). L-Cysteine capped cadmium sulfide quantum dots (L-Cyst-CdS QDs) were proposed as a chiral probe. The CD spectrum of L-Cyst-CdS QDs was significantly changed in the presence of Ni(2+) and Co(2+). On the other hand, other studied cations did not alter the original CD spectrum. Moreover, when increasing the concentration of Ni(2+) or Co(2+), the intensity of the CD spectrum linearly increased as a function of concentration and could be useful for the quantitative analysis. The proposed CD sensor showed linear working concentration ranges of 10-60 μM and 4-80 μM with low detection limits of 7.33 μМ and 1.13 μM for the detection of Ni(2+) and Co(2+), respectively. Parameters possibly affected the detection sensitivity such as solution pH and incubation time were studied and optimized. The proposed sensor was applied to detect Ni(2+) and Co(2+) in real water samples, and the results agreed well with the analysis using the standard ICP-OES. PMID:25813022

  6. Amorphous silicon/polycrystalline thin film solar cells

    SciTech Connect

    Ullal, H.S.

    1991-03-13

    An improved photovoltaic solar cell is described including a p-type amorphous silicon layer, intrinsic amorphous silicon, and an n-type polycrystalline semiconductor such as cadmium sulfide, cadmium zinc sulfide, zinc selenide, gallium phosphide, and gallium nitride. The polycrystalline semiconductor has an energy bandgap greater than that of the amorphous silicon. The solar cell can be provided as a single-junction device or a multijunction device.

  7. Ternary spinel cadmium stannate, cadmium indate, and zinc stannate and binary tin oxide and indium oxide transparent conducting oxides as front contact materials for cadmium sulfide/cadmium tellurium photovoltaic devices

    NASA Astrophysics Data System (ADS)

    Mamazza, Robert, Jr.

    Transparent conducting oxides (TCO's) of Cd2SnO 4 (cadmium stannate), CdIn2O4 (cadmium indate), and Zn2SnO4 (zinc stannate) thin films were investigated from a materials and applications point of view through. All films were deposited by co-sputtering using either binary oxide or metallic (reactive sputtering) targets. The film properties were investigated as a function of film composition and stoichiometry. The effect of process parameters such as deposition temperatures, and post-deposition heat treatments on the structural and electro-optical properties of the films were also investigated extensively. All as-deposited films were found to be amorphous independent of substrate deposition temperature. The electro-optical and crystallographic properties were heavily dependant on the post deposition heat treatments. Cd2SnO4, Zn 2SnO4, and CdIn2O4 all produced highly transparent films with average transmission values (400--900 nm range) of 92%, 93%, and 90%, respectively. Cd2SnO4 and CdIn 2O4 were highly conductive with resistivity values as low as 2.01 x 10-4 O-cm and 2.90 x 10 -4 O-cm, respectively. Conversely, Zn2SnO 4 was not able to produce highly conductive films, with the lowest resistivity being 4.3 x 10-3 O-cm. CdTe solar cells were fabricated using al the above materials as front contacts or as high-ρ layers in bi-layer structures. All cells were of the superstrate configuration: Low-ρ TCO/high-ρ TCO/CdS/CdTe/Back contact. Only the TCO layers were varied; the remainder of the device was held constant. In most cases the inclusion of a high-ρ TCO layer was found to improve solar cell performance, especially in regard to the open circuit voltage. Cd2SnO4 was the exception. The incorporation of Zn2SnO4 as a high-ρ layer enabled a greatest current collection from high energy wavelengths through an apparent thinning effect on the CdS. This increased the overall short circuit current density to values in excess of 24.9 mA/cm2. The standard device consisted of

  8. Cadmium-sulfide crystallites in Cd-. gamma. -glutamyl peptide complexes from Lycopersicon and Daucus

    SciTech Connect

    Reese, R.N. ); Winge, D.R. )

    1989-04-01

    Hydroponically-grown tomato plants (Lycopersicon esculentum P. Mill. cv stone) and suspension-cultured carrot cells (Daucus carota L.) exposed to 100 {mu}M cadmium salts produced metal-{gamma}-glutamyl peptide complexes containing acid labile sulfur. The properties of the complexes resemble the Cd-{gamma}-glutamyl complexes from Schizosaccharomyces pombe and Candida glabrata, known to contain a CdS crystallite core. The crystallite core is stabilized by a coating of peptides of the general structure ({gamma}-Glu-Cys){sub n}-Gly. The Cd-peptide complexes contain predominantly peptides of n{sub 2}, n{sub 3}, n{sub 4} and n{sub 3}desGly. Zn-peptide complexes were also isolated from carrot cultures grown in MS medium supplemented with 2 mM Zn and cysteine. Results of preliminary characterization of these complexes are consistent with the presence of a colloidal particle similar to that of the Cd-complexes.

  9. Cadmium

    Integrated Risk Information System (IRIS)

    Cadmium ; CASRN 7440 - 43 - 9 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Noncarcinogenic Effects

  10. Inorganic-organic solar cells based on quaternary sulfide as absorber materials.

    PubMed

    Hong, Tiantian; Liu, Zhifeng; Yan, Weiguo; Liu, Junqi; Zhang, Xueqi

    2015-12-14

    We report a novel promising quaternary sulfide (CuAgInS) to serve as a semiconductor sensitizer material in the photoelectrochemical field. In this study, CuAgInS (CAIS) sulfide sensitized ZnO nanorods were fabricated on ITO substrates through a facile and low-cost hydrothermal chemical method and applied on photoanodes for solar cells for the first time. The component and stoichiometry were key factors in determining the photoelectric performance of CAIS sulfide, which were controlled by modulating their reaction time. ZnO/Cu0.7Ag0.3InS2 nanoarrays exhibit an enhanced optical and photoelectric performance and the power conversion efficiency of ITO/ZnO/Cu0.7Ag0.3InS2/P3HT/Pt solid-state solar cell was up to 1.80%. The remarkable performance stems from improved electron transfer, a higher efficiency of light-harvesting and appropriate band gap alignment at the interface of the ZnO/Cu0.7Ag0.3InS2 NTs. The research indicates that CAIS as an absorbing material has enormous potential in solar cell systems.

  11. Inorganic-organic solar cells based on quaternary sulfide as absorber materials.

    PubMed

    Hong, Tiantian; Liu, Zhifeng; Yan, Weiguo; Liu, Junqi; Zhang, Xueqi

    2015-12-14

    We report a novel promising quaternary sulfide (CuAgInS) to serve as a semiconductor sensitizer material in the photoelectrochemical field. In this study, CuAgInS (CAIS) sulfide sensitized ZnO nanorods were fabricated on ITO substrates through a facile and low-cost hydrothermal chemical method and applied on photoanodes for solar cells for the first time. The component and stoichiometry were key factors in determining the photoelectric performance of CAIS sulfide, which were controlled by modulating their reaction time. ZnO/Cu0.7Ag0.3InS2 nanoarrays exhibit an enhanced optical and photoelectric performance and the power conversion efficiency of ITO/ZnO/Cu0.7Ag0.3InS2/P3HT/Pt solid-state solar cell was up to 1.80%. The remarkable performance stems from improved electron transfer, a higher efficiency of light-harvesting and appropriate band gap alignment at the interface of the ZnO/Cu0.7Ag0.3InS2 NTs. The research indicates that CAIS as an absorbing material has enormous potential in solar cell systems. PMID:26553746

  12. Sulfidation of electrodeposited microcrystalline/nanocrystalline cuprous oxide thin films for solar energy applications

    NASA Astrophysics Data System (ADS)

    Jayathilaka, K. M. D. C.; Kapaklis, V.; Siripala, W.; Jayanetti, J. K. D. S.

    2012-12-01

    Grain size of polycrystalline semiconductor thin films in solar cells is optimized to enhance the efficiency of solar cells. This paper reports results on an investigation carried out on electrodeposited n-type cuprous oxide (Cu2O) thin films on Ti substrates with small crystallites and sulfidation of them to produce a thin-film solar cell. During electrodeposition of Cu2O films, pH of an aqueous acetate bath was optimized to obtain films of grain size of about 100 nm, that were then used as templates to grow thicker n-type nanocrystalline Cu2O films. XRD and SEM analysis revealed that the films were of single phase and the substrates were well covered by the films. A junction of Cu2O/CuxS was formed by partially sulfiding the Cu2O films using an aqueous sodium sulfide solution. It was observed that the photovoltaic properties of nano Cu2O/CuxS heterojunction structures are better than micro Cu2O/CuxS heterojunction solar cells. Resulting Ti/nano Cu2O/CuxS/Au solar cell structure produced an energy conversion efficiency of 0.54%, Voc = 610 mV and Jsc = 3.4 mA cm-2, under AM 1.5 illumination. This is a significant improvement compared to the use of microcrystalline thin film Cu2O in the solar cell structure where the efficiency of the cell was limited to 0.11%. This improvement is attributed mainly to the increased film surface area associated with nanocrystalline Cu2O films.

  13. A comparative study of the annealing behavior of Cu(In,Ga)(S,Se){sub 2} based solar cells with an indium sulfide buffer layer, partly submitted to wet chemical treatments

    SciTech Connect

    Hönes, C.; Hackenberg, J.; Zweigart, S.; Wachau, A.; Hergert, F.; Siebentritt, S.

    2015-03-07

    Indium sulfide thin films deposited via thermal evaporation from compound source material have been successfully utilized as a cadmium free buffer layer for Cu(In,Ga)Se{sub 2} based solar cells. However, high efficiencies are only reached after an additional annealing step. In this work, the annealing behavior of Cu(In,Ga)(S,Se){sub 2} based indium sulfide buffered solar cells is compared to the annealing behavior of similar cells, which were submitted to wet chemical treatments partly containing cadmium ions. Upon annealing a significant improvement of the initial solar cell characteristics is observed for the untreated cell and is related to the increase of activation energy for the carrier recombination process and a decrease of the ideality factor within the one diode model. It is shown here that this improvement can also be achieved by wet treatments of the absorber prior to buffer layer deposition. Upon annealing these treated cells still gain in collection length but lose open circuit voltage, which is explained here within a model including a highly p-doped absorber surface layer and supported by simulations showing that a decrease in doping density of such a surface layer would lead to the observed effects.

  14. Photophysical studies of chromium sensitizers designed for excited state hole transfer to semiconductors and sequential hole/electron transfers from photoexcited cadmium sulfide nanorods to mononuclear ruthenium water-oxidation catalysts

    NASA Astrophysics Data System (ADS)

    Tseng, Huan-Wei

    a photoexcited cadmium sulfide nanorod and [Ru(diethyl 2,2'-bipyridine-4,4'-dicarboxylate)(2,2':6',2"-terpyridine)Cl] +, a mononuclear water-oxidation catalyst. Upon photoexcitation, hole transfer from the cadmium sulfide nanorod oxidizes the catalyst (Ru 2+ → Ru3+) on a 100 ps to 1 ns timescale. This is followed by electron transfer (10-100 ns) from the nanorod to reduce the Ru3+ center. The relatively slow electron transfer dynamics may provide opportunities for the accumulation of multiple holes at the catalyst, which is required for water oxidation.

  15. Chemically deposited thin films of sulfides and selenides of antimony and bismuth as solar energy materials

    NASA Astrophysics Data System (ADS)

    Nair, M. T.; Nair, Padmanabhan K.; Garcia, V. M.; Pena, Y.; Arenas, O. L.; Garcia, J. C.; Gomez-Daza, O.

    1997-10-01

    Chemical bath deposition techniques for bismuth sulfide, bismuth selenide, antimony sulfide, and antimony selenide thin films of about 0.20 - 0.25 micrometer thickness are reported. All these materials may be considered as solar absorber films: strong optical absorption edges, with absorption coefficient, (alpha) , greater than 104 cm-1, are located at 1.31 eV for Bi2Se3, 1.33 eV for Bi2S3, 1.8 eV for Sb2S3, and 1.35 eV for Sb2Se3. As deposited, all the films are nearly amorphous. However, well defined crystalline peaks matching bismuthinite (JCPDS 17- 0320), paraguanajuatite (JCPDS 33-0214), and stibnite (JCPDS 6-0474) and antimony selenide (JCPDS 15-0861) for Bi2S3, Bi2Se3, Sb2S3 and Sb2Se3 respectively, are observed when the films are annealed in nitrogen at 300 degrees Celsius. This is accompanied by a substantial modification of the electrical conductivity in the films: from 10-7 (Omega) -1 cm-1 (in as prepared films) to 10 (Omega) -1 cm-1 in the case of bismuth sulfide and selenide films, and enhancement of photosensitivity in the case of antimony sulfide films. The chemical deposition of a CuS/CuxSe film on these Vx- VIy films and subsequent annealing at 300 degrees Celsius for 1 h at 1 torr of nitrogen leads to the formation of p-type films (conductivity of 1 - 100 (Omega) -1 cm-1) of multinary composition. Among these, the formation of Cu3BiS3 (JCPDS 9-0488) and Cu3SbS4 (JCPDS 35- 0581), CuSbS2 (JCPDS 35-0413) have been clearly detected. Solar energy applications of these films are suggested.

  16. Cadmium sulfide/copper ternary heterojunction cell research. Final report, January 8, 1979-June 7, 1980

    SciTech Connect

    Fleming, D. L.

    1980-01-01

    Dual source, Se and CuInSe/sub 2/, coevaporation and flash evaporation of stoichiometric CuInSe/sub 2/ powder were investigated to develop a process of fabricating large area CdS/CuInSe/sub 2/ heterojunction solar cells. CuInSe/sub 2/ was seen to decompose upon evaporation, producing layered films in the dual source system. Annealing of these films and alternative dual sources have been considered. Single phase p type films have been produced but no devices have been made from such films. Flash evaporation circumvents the decomposition problem, and if one bakes the powder to obtain a small Cu excess as well as getting a Se excess in the film, p type CuInSe/sub 2/ films can be obtained. A 1% efficient device of 6 cm/sup 2/ area was made using a flash evaporated CuInSe/sub 2/ film. Annealing studies and measurements of spatial uniformity of this device are reported.

  17. Workshop proceedings: Photovoltaic conversion of solar energy for terrestrial applications. Volume 1: Working group and panel reports

    NASA Technical Reports Server (NTRS)

    1973-01-01

    Technological aspects of solar energy conversion by photovoltaic cells are considered. The advantage of the single crystal silicon solar cell approach is developed through comparisons with polycrystalline silicon, cadmium sulfide/copper sulfide thin film cells, and other materials and devices.

  18. Thin film cadmium telluride solar cells. Final technical report, July 1, 1979-August 31, 1980

    SciTech Connect

    Chu, T.L.

    1980-08-01

    Efforts during this program have been directed to the construction of apparatus for the chemical vapor deposition of cadmium telluride films, the selection and preparation of substrates, the deposition and characterization of cadmium telluride films, and the fabrication and characterization of solar cells. Cadmium telluride films have been deposited on a number of substrates by the direct combination of cadmium and tellurium on the substrate surface at 500/sup 0/C or higher at rates of up to 0.6 ..mu..m/min. The structural, crystallographic, and electrical properties of cadmium telluride films deposited over a wide range of conditions have been evaluated. A series of doping experiments have been carried out using iodine and indium as the n-type dopant, and phosphorus, arsenic, and antimony as the p-type dopant. Low resistivity films have not been produced thus far. In/W/graphite substrates have been used for the deposition of n-type films with an ohmic interface. However, no suitable substrates have been found to form an ohmic interface with p-type films. Solar cells prepared from these films exhibit relatively good short-circuit current density, up to 15 mA/cm/sup 2/, but their conversion efficiencies are severely limited by the high series resistance of the devices. It is believed that low resistivity cadmium telluride films can be prepared by optimizing the deposition conditions. In parallel with the search of substrates with low interface resistance, back wall cells, such as p-CdTe/n-CdS/ITO/glass(substrate), should be investigated.

  19. Direct Synthesis of Novel and Reactive Sulfide-modified Nano Iron through Nanoparticle Seeding for Improved Cadmium-Contaminated Water Treatment.

    PubMed

    Su, Yiming; Adeleye, Adeyemi S; Huang, Yuxiong; Zhou, Xuefei; Keller, Arturo A; Zhang, Yalei

    2016-01-01

    Magnetic sulfide-modified nanoscale zerovalent iron (S-nZVI) is of great technical and scientific interest because of its promising application in groundwater remediation, although its synthesis is still a challenge. We develop a new nanoparticle seeding method to obtain a novel and reactive nanohybrid, which contains an Fe(0) core covered by a highly sulfidized layer under high extent of sulfidation. Syntheses monitoring experiments show that seeding accelerates the reduction rate from Fe(2+) to Fe(0) by 19%. X-ray adsorption near edge structure (XANES) spectroscopy and extended X-ray absorption fine structure analyses demonstrate the hexahedral Fe-Fe bond (2.45 and 2.83 Å) formation through breaking down of the 1.99 Å Fe-O bond both in crystalline and amorphous iron oxide. The XANES analysis also shows 24.2% (wt%) of FeS with bond length of 2.4 Å in final nanohybrid. Both X-ray diffraction and Mössbauer analyses further confirm that increased nanoparticle seeding results in formation of more Fe(0) crystals. Nano-SiO2 seeding brings down the size of single Fe(0) grain from 32.4 nm to 18.7 nm, enhances final Fe(0) content from 5.9% to 55.6%, and increases magnetization from 4.7 to 65.5 emu/g. The synthesized nanohybrid has high cadmium removal capacity and holds promising prospects for treatment of metal-contaminated water.

  20. High-performance cadmium sulphide-based planar perovskite solar cell and the cadmium sulphide/perovskite interfaces

    NASA Astrophysics Data System (ADS)

    Peng, Haitao; Sun, Weihai; Li, Yunlong; Yan, Weibo; Yu, Pingrong; Zhou, Huanping; Bian, Zuqiang; Huang, Chunhui

    2016-04-01

    Planar heterojunction perovskite solar cell is one of the most competitive photovoltaic technologies, while charge transport materials play a crucial role. We successfully demonstrated an effective electron transport material, namely chemical bath deposited cadmium sulphide (CdS) film under low temperature, in perovskite-based solar cells. Power conversion efficiency of 16.1% has been achieved, which is comparable to that of devices based on TiO2 film prepared via low-temperature processes. Electronic impedance spectra reveal that the CdS-based device presents a higher recombination resistance than TiO2-based devices, which reduces carrier recombination and increases the open circuit voltage. The interface between CdS and perovskite was characterized with improved characteristics when compared to TiO2, e.g., efficient carrier extraction and reduced surface defect-associated degradation in the devices, which help to alleviate anomalous hysteresis and long-term instability. Furthermore, the entire device was fabricated via solution process with a processing temperature below 100°C, suggesting a promising method of further development of perovskite solar cells and commercial manufacturing.

  1. Cadmium telluride solar cells: Record-breaking voltages

    SciTech Connect

    Poplawsky, Jonathan D.

    2016-01-01

    Here, the performance of CdTe solar cells — cheaper alternatives to silicon photovoltaics — is hampered by their low output voltages, which are normally well below the theoretical limit. Now, record voltages of over 1 V have been reported in single-crystal CdTe heterostructure solar cells, which are close to those of benchmark GaAs cells.

  2. The impact of sodium contamination in tin sulfide thin-film solar cells

    NASA Astrophysics Data System (ADS)

    Steinmann, Vera; Brandt, Riley E.; Chakraborty, Rupak; Jaramillo, R.; Young, Matthew; Ofori-Okai, Benjamin K.; Yang, Chuanxi; Polizzotti, Alex; Nelson, Keith A.; Gordon, Roy G.; Buonassisi, Tonio

    2016-02-01

    Through empirical observations, sodium (Na) has been identified as a benign contaminant in some thin-film solar cells. Here, we intentionally contaminate thermally evaporated tin sulfide (SnS) thin-films with sodium and measure the SnS absorber properties and solar cell characteristics. The carrier concentration increases from 2 × 1016 cm-3 to 4.3 × 1017 cm-3 in Na-doped SnS thin-films, when using a 13 nm NaCl seed layer, which is detrimental for SnS photovoltaic applications but could make Na-doped SnS an attractive candidate in thermoelectrics. The observed trend in carrier concentration is in good agreement with density functional theory calculations, which predict an acceptor-type NaSn defect with low formation energy.

  3. Photoemf in cadmium sulfide

    NASA Technical Reports Server (NTRS)

    Boeer, K. W.

    1971-01-01

    Theoretical and experimental investigations on CdS single crystals and CuxS:CdS photovoltaic cells prepared from CdS single crystals by a chemical-dip procedure are described. The studies are aimed at clarifying cell mechanisms which affect key cell properties (efficiency, reliability, and lifetime) by examining the properties of intrinsic and extrinsic defects in the junction and surface regions and their effects on carrier transport through these regions. The experimental research described includes studies of thermal, infrared, and field quenching of acceptor-doped CdS crystals; investigation of optical and electrical properties of CuxS:CdS photovoltaic cells (current-voltage characteristics, spectral distribution of photocurrent and photovoltage) and the dependence of these properties on temperature and light intensity; measurement of changes, as a result of heat treatment in ultrahigh vacuum, in the spectral distribution of photoconductivity at room temperature and liquid nitrogen temperature, the luminescence spectrum at liquid nitrogen temperature, and the thermally stimulated current curves of CdS crystals; determination of the effect of irradiation with 150 keV (maximum) X-rays on the spectral distribution of photoconductivity and thermally-stimulated current of CdS crystals; and studies of the effect of growth conditions on the photoconductive properties of CdS crystals.

  4. Solar cell power scanner

    NASA Technical Reports Server (NTRS)

    Evans, J. C., Jr.

    1971-01-01

    System locates high- and low-output regions in cadmium sulfide thin film photovoltaic cells. High resolution photograph shows conversion efficiency of each scanned area. X-Y recorder fed by amplified signal from solar cell also produces power contour map. Photo and map reveal high- and low-conversion-efficiency regions.

  5. Direct Synthesis of Novel and Reactive Sulfide-modified Nano Iron through Nanoparticle Seeding for Improved Cadmium-Contaminated Water Treatment

    NASA Astrophysics Data System (ADS)

    Su, Yiming; Adeleye, Adeyemi S.; Huang, Yuxiong; Zhou, Xuefei; Keller, Arturo A.; Zhang, Yalei

    2016-04-01

    Magnetic sulfide-modified nanoscale zerovalent iron (S-nZVI) is of great technical and scientific interest because of its promising application in groundwater remediation, although its synthesis is still a challenge. We develop a new nanoparticle seeding method to obtain a novel and reactive nanohybrid, which contains an Fe(0) core covered by a highly sulfidized layer under high extent of sulfidation. Syntheses monitoring experiments show that seeding accelerates the reduction rate from Fe2+ to Fe0 by 19%. X-ray adsorption near edge structure (XANES) spectroscopy and extended X-ray absorption fine structure analyses demonstrate the hexahedral Fe-Fe bond (2.45 and 2.83 Å) formation through breaking down of the 1.99 Å Fe-O bond both in crystalline and amorphous iron oxide. The XANES analysis also shows 24.2% (wt%) of FeS with bond length of 2.4 Å in final nanohybrid. Both X-ray diffraction and Mössbauer analyses further confirm that increased nanoparticle seeding results in formation of more Fe0 crystals. Nano-SiO2 seeding brings down the size of single Fe0 grain from 32.4 nm to 18.7 nm, enhances final Fe0 content from 5.9% to 55.6%, and increases magnetization from 4.7 to 65.5 emu/g. The synthesized nanohybrid has high cadmium removal capacity and holds promising prospects for treatment of metal-contaminated water.

  6. Direct Synthesis of Novel and Reactive Sulfide-modified Nano Iron through Nanoparticle Seeding for Improved Cadmium-Contaminated Water Treatment

    PubMed Central

    Su, Yiming; Adeleye, Adeyemi S.; Huang, Yuxiong; Zhou, Xuefei; Keller, Arturo A.; Zhang, Yalei

    2016-01-01

    Magnetic sulfide-modified nanoscale zerovalent iron (S-nZVI) is of great technical and scientific interest because of its promising application in groundwater remediation, although its synthesis is still a challenge. We develop a new nanoparticle seeding method to obtain a novel and reactive nanohybrid, which contains an Fe(0) core covered by a highly sulfidized layer under high extent of sulfidation. Syntheses monitoring experiments show that seeding accelerates the reduction rate from Fe2+ to Fe0 by 19%. X-ray adsorption near edge structure (XANES) spectroscopy and extended X-ray absorption fine structure analyses demonstrate the hexahedral Fe-Fe bond (2.45 and 2.83 Å) formation through breaking down of the 1.99 Å Fe-O bond both in crystalline and amorphous iron oxide. The XANES analysis also shows 24.2% (wt%) of FeS with bond length of 2.4 Å in final nanohybrid. Both X-ray diffraction and Mössbauer analyses further confirm that increased nanoparticle seeding results in formation of more Fe0 crystals. Nano-SiO2 seeding brings down the size of single Fe0 grain from 32.4 nm to 18.7 nm, enhances final Fe0 content from 5.9% to 55.6%, and increases magnetization from 4.7 to 65.5 emu/g. The synthesized nanohybrid has high cadmium removal capacity and holds promising prospects for treatment of metal-contaminated water. PMID:27095387

  7. Direct Synthesis of Novel and Reactive Sulfide-modified Nano Iron through Nanoparticle Seeding for Improved Cadmium-Contaminated Water Treatment.

    PubMed

    Su, Yiming; Adeleye, Adeyemi S; Huang, Yuxiong; Zhou, Xuefei; Keller, Arturo A; Zhang, Yalei

    2016-01-01

    Magnetic sulfide-modified nanoscale zerovalent iron (S-nZVI) is of great technical and scientific interest because of its promising application in groundwater remediation, although its synthesis is still a challenge. We develop a new nanoparticle seeding method to obtain a novel and reactive nanohybrid, which contains an Fe(0) core covered by a highly sulfidized layer under high extent of sulfidation. Syntheses monitoring experiments show that seeding accelerates the reduction rate from Fe(2+) to Fe(0) by 19%. X-ray adsorption near edge structure (XANES) spectroscopy and extended X-ray absorption fine structure analyses demonstrate the hexahedral Fe-Fe bond (2.45 and 2.83 Å) formation through breaking down of the 1.99 Å Fe-O bond both in crystalline and amorphous iron oxide. The XANES analysis also shows 24.2% (wt%) of FeS with bond length of 2.4 Å in final nanohybrid. Both X-ray diffraction and Mössbauer analyses further confirm that increased nanoparticle seeding results in formation of more Fe(0) crystals. Nano-SiO2 seeding brings down the size of single Fe(0) grain from 32.4 nm to 18.7 nm, enhances final Fe(0) content from 5.9% to 55.6%, and increases magnetization from 4.7 to 65.5 emu/g. The synthesized nanohybrid has high cadmium removal capacity and holds promising prospects for treatment of metal-contaminated water. PMID:27095387

  8. Thin film cadmium telluride solar cells. Final technical report for period July 1, 1979-August 31, 1980

    SciTech Connect

    Chu, T.L.

    1980-08-01

    The objectives of this contract are to investigate thin films of cadmium telluride on low cost substrates and to determine the feasibility of using these films for high efficiency solar cells. Efforts during this program have been directed to the construction of apparatus for the chemical vapor deposition of cadmium telluride films, the selection and preparation of substrates, the deposition and characterization of cadmium telluride films, and the fabrication and characterization of solar cells. Cadmium telluride films have been deposited on a number of substrates by the direct combination of cadmium and tellurium on the substrate surface at 500/sup 0/C or higher at rates of up to 0.6 ..mu..m/min. The structural, crystallographic, and electrical properties of cadmium telluride films deposited over a wide range of conditions have been evaluated. A series of doping experiments have been carried out using iodine and indium as the n-type dopant, and phosphorus, arsenic, and antimony as the p-type dopant. Low resistivity films have not been produced thus far. In/W/graphite substrates have been used for the deposition of n-type films with an ohmic interface. However, no suitable substrates have been found to form an ohmic interface with p-type films. Solar cells prepared from these films exhibit relatively good short-circuit current density, up to 15 mA/cm/sup 2/, but their conversion efficiencies are severely limited by the high series resistance of the devices.

  9. Atomic layer deposition of titanium sulfide and its application in extremely thin absorber solar cells

    SciTech Connect

    Mahuli, Neha; Sarkar, Shaibal K.

    2015-01-15

    Atomic layer deposition (ALD) of TiS{sub 2} is investigated with titanium tetrachloride and hydrogen sulfide precursors. In-situ quartz crystal microbalance and ex-situ x-ray reflectivity measurements are carried out to study self-limiting deposition chemistry and material growth characteristics. The saturated growth rate is found to be ca. 0.5 Å/cycle within the ALD temperature window of 125–200 °C. As grown material is found poorly crystalline. ALD grown TiS{sub 2} is applied as a photon harvesting material for solid state sensitized solar cells with TiO{sub 2} as electron transport medium. Initial results with Spiro-OMeTAD as hole conducting layer show ca. 0.6% energy conversion efficiency under 1 sun illumination.

  10. Workshop proceedings: Photovoltaic conversion of solar energy for terrestrial applications. Volume 2: Invited papers

    NASA Technical Reports Server (NTRS)

    1973-01-01

    A photovoltaic device development plan is reported that considers technological as well as economical aspects of single crystal silicon, polycrystal silicon, cadmium sulfide/copper sulfide thin films, as well as other materials and devices for solar cell energy conversion systems.

  11. Synthesis of Copper-Antimony-Sulfide Nanocrystals for Solution-Processed Solar Cells.

    PubMed

    Suehiro, Satoshi; Horita, Keisuke; Yuasa, Masayoshi; Tanaka, Tooru; Fujita, Katsuhiko; Ishiwata, Yoichi; Shimanoe, Kengo; Kida, Tetsuya

    2015-08-17

    The p-type nanocrystals (NCs) of copper-based chalcogenides, such as CuInSe2 and Cu2ZnSnS4, have attracted increasing attention in photovoltaic applications due to their potential to produce cheap solution-processed solar cells. Herein, we report the synthesis of copper-antimony-sulfide (CAS) NCs with different crystal phases including CuSbS2, Cu3SbS4, and Cu12Sb4S13. In addition, their morphology, crystal phase, and optical properties were characterized using transmission electron microscopy, X-ray diffractometry, UV-vis-near-IR spectroscopy, and photoemission yield spectroscopy. The morphology, crystal phase, and electronic structure were significantly dependent on the chemical composition in the CAS system. Devices were fabricated using particulate films consisting of CAS NCs prepared by spin coating without a high-temperature treatment. The CAS NC-based devices exhibited a diode-like current-voltage characteristic when coupled with an n-type CdS layer. In particular, the CuSbS2 NC devices exhibited photovoltaic responses under simulated sunlight, demonstrating its applicability for use in solution-processed solar cells.

  12. Photon correlation spectroscopic and spectrophotometric studies of the formation of cadmium sulfide nanoparticles in ammonia-thiourea solutions

    NASA Astrophysics Data System (ADS)

    Bulavchenko, A. I.; Kolodin, A. N.; Podlipskaya, T. Yu.; Demidova, M. G.; Maksimovskii, E. A.; Beizel', N. F.; Larionov, S. V.; Okotrub, A. V.

    2016-05-01

    Nucleation of CdS in an aqueous ammonia solution of thiourea and cadmium chloride was studied by photon correlation spectroscopy (PCS), static light scattering, and spectrophotometry. The hydrodynamic diameter of nanoparticles, light scattering intensity, and optical density of the solutions increased with temperature and synthesis time. The processes of formation, growth, and coagulation of nanoparticles can be transferred from solution to the filter surface by continuously filtering the reaction mixture through a 200-nm filter.

  13. Energy level alignment in TiO2/metal sulfide/polymer interfaces for solar cell applications.

    PubMed

    Lindblad, Rebecka; Cappel, Ute B; O'Mahony, Flannan T F; Siegbahn, Hans; Johansson, Erik M J; Haque, Saif A; Rensmo, Håkan

    2014-08-28

    Semiconductor sensitized solar cell interfaces have been studied with photoelectron spectroscopy to understand the interfacial electronic structures. In particular, the experimental energy level alignment has been determined for complete TiO2/metal sulfide/polymer interfaces. For the metal sulfides CdS, Sb2S3 and Bi2S3 deposited from single source metal xanthate precursors, it was shown that both driving forces for electron injection into TiO2 and hole transfer to the polymer decrease for narrower bandgaps. The energy level alignment results were used in the discussion of the function of solar cells with the same metal sulfides as light absorbers. For example Sb2S3 showed the most favourable energy level alignment with 0.3 eV driving force for electron injection and 0.4 eV driving force for hole transfer and also the most efficient solar cells due to high photocurrent generation. The energy level alignment of the TiO2/Bi2S3 interface on the other hand showed no driving force for electron injection to TiO2, and the performance of the corresponding solar cell was very low.

  14. Cadmium Telluride Solar Cells on Ultrathin Glass for Space Applications

    NASA Astrophysics Data System (ADS)

    Irvine, S. J. C.; Lamb, D. A.; Clayton, A. J.; Kartopu, G.; Barrioz, V.

    2014-08-01

    This paper details the preliminary findings of a study to achieve a durable thin-film CdTe photovoltaic (PV) device structure on ultrathin space-qualified cover glass. An aluminum-doped zinc oxide (AZO) transparent conducting oxide was deposited directly onto the cover glass using metalorganic chemical vapor deposition (MOCVD). The AZO demonstrated low sheet resistance of 10 Ω/□ and high optical transparency of 85% as well as excellent adherence and environmental stability. Preliminary deposition of PV layers onto the AZO on cover glass, by MOCVD, showed the possibility of such a structure, yielding a device conversion efficiency of 7.2%. High series resistance (10 Ω cm2) and low V oc (586 mV) were identified as the limiting factors when compared with the authors' platform process on indium tin oxide-coated aluminosilicate. The coverage of the Cd1- x Zn x S window layer along with the front contacting of the device were shown to be the major causes of the low efficiency. Further deposition of AZO/CdTe employing an oxygen plasma cleaning step to the cover glass and evaporated gold front contacts significantly improved the device performance. With a highest conversion efficiency of 10.2%, series resistance improved to 4.4 Ω cm2, open-circuit voltage ( V oc) up to 667 mV, and good adhesion, this represents the first demonstration of direct deposition of CdTe solar cells onto 100- μm-thick space-qualified cover glass.

  15. Annealed single-crystal cadmium selenide electrodes in liquid junction solar cells

    NASA Astrophysics Data System (ADS)

    Wessel, S.; Mackintosh, A.; Colbow, K.

    1984-12-01

    I-V characteristics, voltage dependence of the quantum efficiency, and spectral response were compared for annealed single-crystal CdSe photoanodes. Annealing in cadmium atmosphere improved the overall solar response considerably, while annealing under vacuum revealed a poor response for photon energies larger than 1.8 eV and a high quantum efficiency for near-bandgap energies. This behavior may be attributed to electron-hole pair generation from interbandgap states and a large density of minority carrier recombination centers near the crystal surface, owing to a high nonstoichiometry and a selenium layer at the surface. Annealing in selenium atmosphere resulted in very poor solar response caused by compensation. Simultaneous illumination of the electrodes with a He-Ne laser strongly enhanced the quantum efficiency for vacuum-annealed crystals for near-bandgap photons. We attribute this to electron trapping in the selenium-rich surface, with a resulting increase in depletion-layer width in the cadmium selenide.

  16. Performance optimization of solar cells based on colloidal lead sulfide nanocrystals

    SciTech Connect

    Ulfa, Maria

    2014-02-24

    Colloidal semiconducting quantum dot nanocrystals (NCs) have attracted extensive interest as active building-block for low-cost solution-processed photovoltaic due to their size tunable absorption from the visible to near IR. Among various nanocrystal composition, lead sulfide (PbS), having a bulk bandgap of 0.41 eV, are particularly attractive for photovoltaic applications due to their excellent photosensitivity in the near IR. Starting from colloidal synthesis, in this project functional solar cells are fabricated and characterized based on the nearly monodispersed colloidal PbS nanocrystals that we synthesized. These NC-solar cells are fabricated under a “depleted heterojunction” device architecture containing a planar “tipe II” heretojunction formed by a layer of electron-transporting TiO{sub 2} and a layer of PbS NCs. Relevant structural, optical, and electrical characterizations are performed on NCs and their devices. To understand the operational mechanism of these NC-based solar cells, various material and device aspects are investigated in this work aiming for optimized photovoltaic performance. These aspects include the effect of: (1) NC dimensions (and thus their band gaps); (2) passivation of surface traps through post-synthesis treatments; (3) NC surface ligand-exchange; and (4) interfacial modifications at the heterojunction. The most optimized photovoltaic performance is found after combining the surface trap passivation strategy by halides, ligand-exchange by 3-mercaptopropionic acids, and interfacial TiCl4 treatment, leading to a peak open-circuit voltage of 0.53 V, a short-circuit current density of 14.03 mAcm{sup −2}, and a power conversion efficiency of 3.25%.

  17. Synthesis and structural characterization of magnetic cadmium sulfide-cobalt ferrite nanocomposite, and study of its activity for dyes degradation under ultrasound

    NASA Astrophysics Data System (ADS)

    Farhadi, Saeed; Siadatnasab, Firouzeh

    2016-11-01

    Cadmium sulfide-cobalt ferrite (CdS/CFO) nanocomposite was easily synthesized by one-step hydrothermal decomposition of cadmium diethyldithiocarbamate complex on the CoFe2O4 nanoparticles at 200 °C. Spectroscopic techniques of powder X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FT-IR), UV-visible spectroscopy, field emission scanning electron microscopy (FESEM), energy-dispersive X-ray spectroscopy (EDX), Brunauer-Emmett-Teller (BET), and magnetic measurements were applied for characterizing the structure and morphology of the product. The results of FT-IR, XRD and EDX indicated that the CdS/CFO was highly pure. SEM and TEM results revealed that the CdS/CFO nanocomposite was formed from nearly uniform and sphere-like nanoparticles with the size of approximately 20 nm. The UV-vis absorption spectrum of the CdS/CFO nanocomposite showed the band gap of 2.21 eV, which made it suitable for sono-/photo catalytic purposes. By using the obtained CdS/CFO nanocomposite, an ultrasound-assisted advanced oxidation process (AOP) has been developed for catalytic degradation of methylene blue (MB), Rhodamine B (RhB), and methyl orange (MO)) in the presence of H2O2 as a green oxidant. CdS/CFO nanocomposite exhibited excellent sonocatalytic activity, so that, dyes were completely degraded in less than 10 min. The influences of crucial factors such as the H2O2 amount and catalyst dosage on the degradation efficiency were evaluated. The as-prepared CdS/CFO nanocomposite exhibited higher catalytic activity than pure CdS nanoparticles. Moreover, the magnetic property of CoFe2O4 made the nanocomposite recyclable.

  18. The risk to the United Kingdom population of zinc cadmium sulfide dispersion by the Ministry of Defence during the "cold war"

    PubMed Central

    Elliott, P; Phillips, C; Clayton, B; Lachmann, P

    2002-01-01

    Objectives: To estimate exposures to cadmium (Cd) received by the United Kingdom population as a result of the dispersion of zinc Cd sulfide (ZnCdS) by the Ministry of Defence between 1953 and 1964, as a simulator of biological warfare agents. Methods: A retrospective risk assessment study was carried out on the United Kingdom population during the period 1953–64. This determined land and air dispersion of ZnCdS over most of the United Kingdom, inhalation exposure of the United Kingdom population, soil contamination, and risks to personnel operating equipment that dispersed ZnCdS. Results: About 4600 kg ZnCdS were dispersed from aircraft and ships, at times when the prevailing winds would allow large areas of the country to be covered. Cadmium released from 44 long range trials for which data are available, and extrapolated to a total of 76 trials to allow for trials with incomplete information, is about 1.2% of the estimated total release of Cd into the atmosphere over the same period. "Worst case" estimates are 10 µg Cd inhaled over 8 years, equivalent to Cd inhaled in an urban environment in 12–100 days, or from smoking 100 cigarettes. A further 250 kg ZnCdS was dispersed from the land based sites, but significant soil contamination occurred only in limited areas, which were and have remained uninhabited. Of the four personnel involved in the dispersion procedures (who were probably exposed to much higher concentrations of Cd than people on the ground), none are suspected of having related illnesses. Conclusion: Exposure to Cd from dissemination of ZnCdS during the "cold war" should not have resulted in adverse health effects in the United Kingdom population. PMID:11836463

  19. Flower-like nickel cobalt sulfide microspheres modified with nickel sulfide as Pt-free counter electrode for dye-sensitized solar cells

    NASA Astrophysics Data System (ADS)

    Huo, Jinghao; Wu, Jihuai; Zheng, Min; Tu, Yongguang; Lan, Zhang

    2016-02-01

    The nickel cobalt sulfide/nickel sulfide (NiCo2S4/NiS) microspheres which exhibit flower-like morphologies are synthesized by a two-step hydrothermal method. Then the NiCo2S4/NiS microspheres are deposited on a fluorine doped SnO2 substrate by spin-casting the isopropyl alcohol solution of as-prepared microspheres. The cyclic voltammetry, electrochemical impedance spectroscopy and Tafel tests are employed to measure the electrochemical performance of NiCo2S4/NiS counter electrode. The NiCo2S4 and NiS all are used to improve the conductivity and electrocatalytic ability of the films, and the NiS can also increase the specific surface area of microspheres. The dye-sensitized solar cells (DSSCs) with the NiCo2S4/NiS counter electrode exhibite a power conversion efficiency of 8.8%, which is higher than that of DSSC with Pt counter electrode (8.1%) under the light intensity of 100 mW cm-2 (AM 1.5 G).

  20. Photocatalytic Conversion of Nitrobenzene to Aniline through Sequential Proton-Coupled One-Electron Transfers from a Cadmium Sulfide Quantum Dot.

    PubMed

    Jensen, Stephen C; Homan, Stephanie Bettis; Weiss, Emily A

    2016-02-10

    This paper describes the use of cadmium sulfide quantum dots (CdS QDs) as visible-light photocatalysts for the reduction of nitrobenzene to aniline through six sequential photoinduced, proton-coupled electron transfers. At pH 3.6-4.3, the internal quantum yield of photons-to-reducing electrons is 37.1% over 54 h of illumination, with no apparent decrease in catalyst activity. Monitoring of the QD exciton by transient absorption reveals that, for each step in the catalytic cycle, the sacrificial reductant, 3-mercaptopropionic acid, scavenges the excitonic hole in ∼5 ps to form QD(•-); electron transfer to nitrobenzene or the intermediates nitrosobenzene and phenylhydroxylamine then occurs on the nanosecond time scale. The rate constants for the single-electron transfer reactions are correlated with the driving forces for the corresponding proton-coupled electron transfers. This result suggests, but does not prove, that electron transfer, not proton transfer, is rate-limiting for these reactions. Nuclear magnetic resonance analysis of the QD-molecule systems shows that the photoproduct aniline, left unprotonated, serves as a poison for the QD catalyst by adsorbing to its surface. Performing the reaction at an acidic pH not only encourages aniline to desorb but also increases the probability of protonated intermediates; the latter effect probably ensures that recruitment of protons is not rate-limiting.

  1. A selective fluorescence probe for mercury ion based on the fluorescence quenching of terbium(III)-doped cadmium sulfide composite nanoparticles

    NASA Astrophysics Data System (ADS)

    Fu, Jie; Wang, Lun; Chen, Hongqi; Bo, Ling; Zhou, Cailing; Chen, Jingguo

    2010-10-01

    A fluorescent probe for mercury(II) ions, based on the quenching of fluorescence of terbium(III) ions doped in CdS nanoparticles, has been developed. The terbium(III)-doped cadmium sulfide composite nanoparticles were successfully synthesized through a straightforward one-pot process, with the biomolecule glutathione (GSH) as a capping ligand. In addition, the terbium(III) ions were observed an enhancement of emission intensity, owing to fluorescence energy transfer from the excited CdS particles to the emitting terbium(III). Because of a specific interaction, the fluorescence intensity of terbium(III)-doped CdS particles is obviously reduced in the presence of mercury(II) ions. The fluorescence quenching phenomenon of terbium(III) can be attributed to the fact that the energy transfer system was destroyed by combining with mercury(II). Under the optimal conditions, the fluorescent intensity of terbium(III) ions at 491 nm decreased linearly with the concentration of mercury(II) ions ranging from 4.5 nmol L -1 to 550 nmol L -1. The limit of detection for mercury(II) was 0.1 nmol L -1. This method is simple, practical, relatively free of interference from coexisting substances and can be successfully applied to the determination of mercury(II) ions in real water samples. In addition, the probable mechanism of reaction between terbium(III)-doped CdS composite nanoparticles and mercury(II) was also discussed.

  2. Thermo-optical characterization of cadmium selenide/zinc sulfide (CdSe/ZnS) quantum dots embedded in biocompatible materials.

    PubMed

    Pilla, Viviane; Alves, Leandro P; Iwazaki, Adalberto N; Andrade, Acácio A; Antunes, Andrea; Munin, Egberto

    2013-09-01

    Cadmium selenide/zinc sulfide (CdSe/ZnS) core-shell quantum dots (QDs) embedded in biocompatible materials were thermally and optically characterized with a thermal lens (TL) technique. Transient TL measurements were performed with a mode-mismatched, dual-beam (excitation and probe) configuration. A thermo-optical study of the CdSe/ZnS QDs was performed for different core diameters (3.5, 4.0, 5.2, and 6.6 nm) in aqueous solution and synthetic saliva, and three different core diameters (2.4, 2.9, and 4.1 nm) embedded in restorative dental resin (0.025% by mass). The thermal diffusivity results are characteristic of the biocompatible matrices. The radiative quantum efficiencies for aqueous solution and biofluid materials are dependent on the core size of the CdSe/ZnS core-shell QDs. The results obtained from the fluorescence spectral measurements for the biocompatible materials support the TL results.

  3. Different behavior of Staphylococcus epidermidis in intracellular biosynthesis of silver and cadmium sulfide nanoparticles: more stability and lower toxicity of extracted nanoparticles.

    PubMed

    Rezvani Amin, Zohreh; Khashyarmanesh, Zahra; Fazly Bazzaz, Bibi Sedigheh

    2016-09-01

    Chemical reagents that are used for synthesis of nanoparticles are often toxic, while biological reagents are safer and cost-effective. Here, the behavior of Staphylococcus epidermidis (ATCC 12228) was evaluated for biosynthesis of silver nanoparticles (Ag-NPs) and cadmium sulfide nanoparticles (CdS-NPs) using TEM images intra- and extracellularly. The bacteria only biosynthesized the nanoparticles intracellularly and distributed Ag-NPs throughout the cytoplasm and on outside surface of cell walls, while CdS-NPs only formed in cytoplasm near the cell wall. A new method for purification of the nanoparticles was used. TEM images of pure CdS-NPs confirmed biosynthesis of agglomerated nanoparticles. Biosynthetic Ag-NPs were more stable against bright light and aggregation reaction than synthetic Ag-NPs (prepared chemically) also biosynthetic Ag-NPs displayed lower toxicity in in vitro assays. CdS-NPs indicated no toxicity in in vitro assays. Biosynthetic nanoparticles as product of the detoxification pathway may be safer and more stable for biosensors. PMID:27430507

  4. Zelda and company - Petrogenesis of sulfide-rich Fremdlinge and constraints on solar nebula processes

    NASA Technical Reports Server (NTRS)

    Armstrong, John T.; Hutcheon, Ian D.; Wasserburg, G. J.

    1987-01-01

    A detailed petrographic and chemical study of Zelda (a gigantic sulfide-rich Fremdling from the Allende Ca-rich inclusion, CAI, Egg 6) and its contact with the host was conducted using analytical SEM and electron-microprobe techniques, and the results were compared with those obtained on other sulfide-rich and oxide-rich Fremdlinge. Strong evidence is presented that Zelda, a type-example of sulfide-rich Fremdlinge, has been formed from a preexisting Ur-Fremdling, similar by composition to Willy, by closed-system sulfidization of magnetite and metal. At least two different sulfidization mechanisms appear to have occurred in altering Fremdlinge: one producing compositionally homogeneous equigranular objects such as Zelda, the other producing compositionally and texturally heterogeneous objects.

  5. Lead Sulfide Cathode for Quantum Dot Solar Cells: Electrosynthesis and Characterization

    NASA Astrophysics Data System (ADS)

    Van Le, Nghiem; Nguyen, Hoang Thai; Le, Hai Viet; Nguyen, Thoa Thi Phuong

    2016-08-01

    Deposition of lead sulfide (PbS) nanocrystalline thin films onto conducting fluorine-doped tin oxide (FTO) glass has been performed by cyclic voltammetry (CV) in 1.5 mM solution of lead nitrate and sodium thiosulfate at 100 mV s-1 scan rate in the potential range of -1.0 V to 0.0 V versus saturated calomel electrode. X-ray diffraction analysis and scanning electron microscopy revealed formation of cubic PbS crystals with size of 100 nm to 150 nm after 50 cycles. High electrocatalytic activity of the synthesized PbS film for the S2-/S{/n 2-} redox couple, used as a mediator for quantum dot solar cells (QDSCs), was demonstrated by electrochemical impedance spectroscopy and CV measurements. The prepared PbS/FTO was used as a counterelectrode to fabricate PbS-QDSCs with a photoanode consisting of CdS/CdSe quantum dots adsorbed on mesoporous TiO2 film and a polysulfide solution electrolyte. The performance of the PbS-QDSC was compared with a QDSC with a platinum counterelectrode (Pt-QDSC). It was found that, using the same fabrication conditions, the performance of the PbS-QDSC was better than that of the Pt-QDSC. At 1 sun (100 mW cm-2) simulated light, average energy conversion efficiency of 2.14%, short-circuit current of 9.22 mA cm-2, open-circuit potential of 0.50 V, and fill factor of 0.47 were achieved by the fabricated PbS-QDSC.

  6. Cadmium sulfide/graphitic carbon nitride heterostructure nanowire loading with a nickel hydroxide cocatalyst for highly efficient photocatalytic hydrogen production in water under visible light

    NASA Astrophysics Data System (ADS)

    Yan, Zhiping; Sun, Zijun; Liu, Xiang; Jia, Hongxing; Du, Pingwu

    2016-02-01

    Photocatalytic hydrogen production from water in a noble-metal-free system has attracted much attention in recent years. Herein we report on the use of core/shell cadmium sulfide/graphitic carbon nitride (CdS/g-C3N4) heterojunction nanorods modified by nickel hydroxide (Ni(OH)2) as a highly efficient photocatalyst for visible light-driven hydrogen production from water. Due to efficient separation of the photoexcited charge carriers in the CdS/g-C3N4 core/shell nanorods and the synergistic effect of Ni(OH)2, the optimal hydrogen evolution rate over Ni(OH)2-CdS/g-C3N4 is 115.18 μmol h-1 mg-1 under visible light irradiation (λ > 420 nm), which is ~26 times higher than the CdS/g-C3N4 nanorod composite without Ni(OH)2 and ~7 times better than the 0.5 wt% Pt-CdS/g-C3N4 nanorod composite. The apparent quantum efficiency is ~16.7% at an excitation of 450 nm. During photocatalysis, no degradation of Ni(OH)2 was observed based on the XPS data, indicating that it is a robust cocatalyst. Moreover, the present photocatalyst showed excellent photocatalytic stability for hydrogen production and the turnover number (TON) reached ~24 600 over 90 hours.Photocatalytic hydrogen production from water in a noble-metal-free system has attracted much attention in recent years. Herein we report on the use of core/shell cadmium sulfide/graphitic carbon nitride (CdS/g-C3N4) heterojunction nanorods modified by nickel hydroxide (Ni(OH)2) as a highly efficient photocatalyst for visible light-driven hydrogen production from water. Due to efficient separation of the photoexcited charge carriers in the CdS/g-C3N4 core/shell nanorods and the synergistic effect of Ni(OH)2, the optimal hydrogen evolution rate over Ni(OH)2-CdS/g-C3N4 is 115.18 μmol h-1 mg-1 under visible light irradiation (λ > 420 nm), which is ~26 times higher than the CdS/g-C3N4 nanorod composite without Ni(OH)2 and ~7 times better than the 0.5 wt% Pt-CdS/g-C3N4 nanorod composite. The apparent quantum efficiency is ~16.7% at an

  7. Thin film cadmium telluride, zinc telluride, and mercury zinc telluride solar cells

    SciTech Connect

    Chu, T.L. )

    1992-04-01

    This report describes research to demonstrate (1) thin film cadmium telluride solar cells with a quantum efficiency of 75% or higher at 0. 44 {mu}m and a photovoltaic efficiency of 11.5% or greater, and (2) thin film zinc telluride and mercury zinc telluride solar cells with a transparency to sub-band-gap radiation of 65% and a photovoltaic conversion efficiency of 5% and 8%, respectively. Work was directed at (1) depositing transparent conducting semiconductor films by solution growth and metal-organic chemical vapor deposition (MOCVD) technique, (2) depositing CdTe films by close-spaced sublimation (CSS) and MOCVD techniques, (3) preparing and evaluating thin film CdTe solar cells, and (4) preparing and characterizing thin film ZnTe, CD{sub 1-x}Zn{sub 1-x}Te, and Hg{sub 1-x}Zn{sub x}Te solar cells. The deposition of CdS films from aqueous solutions was investigated in detail, and their crystallographic, optical, and electrical properties were characterized. CdTe films were deposited from DMCd and DIPTe at 400{degrees}C using TEGa and AsH{sub 3} as dopants. CdTe films deposited by CSS had significantly better microstructures than those deposited by MOCVD. Deep energy states in CdTe films deposited by CSS and MOCVD were investigated. Thin films of ZnTe, Cd{sub 1- x}Zn{sub x}Te, and Hg{sub 1-x}Zn{sub x}Te were deposited by MOCVD, and their crystallographic, optical, and electrical properties were characterized. 67 refs.

  8. Effect of the Concentration on the X-ray Luminescence Efficiency of a Cadmium Selenide/Zinc Sulfide (CdSe/ZnS) Quantum Dot Nanoparticle Solution

    NASA Astrophysics Data System (ADS)

    Valais, I.; Michail, C.; Nikolopoulos, D.; Fountzoula, C.; Bakas, A.; Yannakopoulos, P.; Fountos, G.; Panayiotakis, G.; Kandarakis, I.

    2015-09-01

    In the current study preliminary results on the luminescence efficiency (LE) of toluene dissolved Cadmium Selenide/Zinc Sulfide (CdSe/ZnS, Sigma-Aldrich, Lumidot 694622) quantum dot samples (QDs) after exposure to X-rays of variable radiation flux are shown. The distinctive influence of the weight over volume (w/v) concentration of the samples in LE was investigated. The light emission of the QDs was additionally measured after UV irradiation. The distribution of the emitted light was symmetrical with a maximum at 590 nm. The w/v concentration of the QDs varied between 7.1×10-5 mg/mL to 28.4×10-5 mg/mL. The samples were handled in a cubic 12.5×12.5×45mm3 quartz cuvette. Each sample was excited under X-ray irradiation, in the energy range from 50 to 130 kVp using a BMI General Medical Merate tube with rotating Tungsten anode and inherent filtration equivalent to 2 mm Al. The X-ray LE, induced by the 28.4×10-5 mg/mL QDs found higher, however, the distinction was vague in the highly concentrated samples. The maximum efficiency was obtained at the 90 kVp for QDs with 21.3×10-5 mg/mL w/v concentration. In the high energy range (120-130 kVp) all concentration levels exhibited comparable X-ray induced LE. The luminescence properties of the investigated QDs appear promising for X-ray detection applications.

  9. Utilization of reduced graphene oxide/cadmium sulfide-modified carbon cloth for visible-light-prompt photoelectrochemical sensor for copper (II) ions.

    PubMed

    Foo, C Y; Lim, H N; Pandikumar, A; Huang, N M; Ng, Y H

    2016-03-01

    A newly developed CdS/rGO/CC electrode was prepared based on a flexible carbon cloth (CC) substrate with cadmium sulfide (CdS) nanoparticles and reduced graphene oxide (rGO). The CdS was synthesized using an aerosol-assisted chemical vapor deposition (AACVD) method, and the graphene oxide was thermally reduced on the modified electrode surface. The existence of rGO in the CdS-modified electrode increased the photocurrent intensity of the CdS/rGO/CC-modified electrode by three orders of magnitude, compared to that of the CdS/ITO electrode and two orders of magnitude higher than the CdS/CC electrode. A new visible-light-prompt photoelectrochemical sensor was developed based on the competitive binding reaction of Cu(2+) and CdS on the electrode surface. The results showed that the effect of the Cu(2+) on the photocurrent response was concentration-dependent over the linear ranges of 0.1-1.0 μM and 1.0-40.0 μM with a detection limit of 0.05 μM. The results of a selectivity test showed that this modified electrode has a high response toward Cu(2+) compared to other heavy metal ions. The proposed CdS/rGO/CC electrode provided a significantly high potential current compared to other reported values, and could be a practical tool for the fast, sensitive, and selective determination of Cu(2+). PMID:26595899

  10. Biochemical and behavioural responses of the marine polychaete Hediste diversicolor to cadmium sulfide quantum dots (CdS QDs): waterborne and dietary exposure.

    PubMed

    Buffet, Pierre-Emmanuel; Poirier, Laurence; Zalouk-Vergnoux, Aurore; Lopes, Christelle; Amiard, Jean-Claude; Gaudin, Pierre; Risso-de Faverney, Christine; Guibbolini, Marielle; Gilliland, Douglas; Perrein-Ettajani, Hanane; Valsami-Jones, Eugenia; Mouneyrac, Catherine

    2014-04-01

    Cadmium sulfide (CdS) quantum dots are widely used in medical imaging. The aim of this study was to examine toxicity effects of CdS engineered nanoparticles (CdS NPs) compared to soluble Cd, on marine ragworms (Hediste diversicolor) exposed for 14 d to these contaminants (10 μg Cd L(-1)) in seawater or via their food (contaminated worm tissue). In our experimental media, Dynamic Light Scattering studies showed that the majority of CdS remained in the nanoscale (1-10 nm) with the exception of few aggregates (100-300 nm). Labile Cd fractions released from CdS NPs were estimated by diffusive gradient in thin films, showing that about 50% of CdS NPs remained in nanoparticulate form. Ragworms accumulated Cd in both soluble Cd and CdS NPs in waterborne exposures only. Greater significant changes of biochemical responses were observed in worms exposed to CdS NPs in seawater compared to contaminated food. Catalase and glutathione-S-transferase activities were the most sensitive biochemical biomarkers responding to both Cd treatments for waterborne exposure. Inductions of CAT were higher in diet-exposed worms to Cd as NPs vs soluble form suggesting a specific "nano" effect. Caspase activities increased in worms exposed to soluble Cd and Cd NPs for the two routes of exposure compared to controls. Defences, may be insufficient to prevent reactive oxygen species generation and the associated apoptosis. Behaviour of invertebrates inside sediment showed impairments of body movements in worms exposed to CdS NPs. This study points out oxidative processes as the main consequences of exposure to Cd based NPs in worms.

  11. Biochemical and behavioural responses of the marine polychaete Hediste diversicolor to cadmium sulfide quantum dots (CdS QDs): waterborne and dietary exposure.

    PubMed

    Buffet, Pierre-Emmanuel; Poirier, Laurence; Zalouk-Vergnoux, Aurore; Lopes, Christelle; Amiard, Jean-Claude; Gaudin, Pierre; Risso-de Faverney, Christine; Guibbolini, Marielle; Gilliland, Douglas; Perrein-Ettajani, Hanane; Valsami-Jones, Eugenia; Mouneyrac, Catherine

    2014-04-01

    Cadmium sulfide (CdS) quantum dots are widely used in medical imaging. The aim of this study was to examine toxicity effects of CdS engineered nanoparticles (CdS NPs) compared to soluble Cd, on marine ragworms (Hediste diversicolor) exposed for 14 d to these contaminants (10 μg Cd L(-1)) in seawater or via their food (contaminated worm tissue). In our experimental media, Dynamic Light Scattering studies showed that the majority of CdS remained in the nanoscale (1-10 nm) with the exception of few aggregates (100-300 nm). Labile Cd fractions released from CdS NPs were estimated by diffusive gradient in thin films, showing that about 50% of CdS NPs remained in nanoparticulate form. Ragworms accumulated Cd in both soluble Cd and CdS NPs in waterborne exposures only. Greater significant changes of biochemical responses were observed in worms exposed to CdS NPs in seawater compared to contaminated food. Catalase and glutathione-S-transferase activities were the most sensitive biochemical biomarkers responding to both Cd treatments for waterborne exposure. Inductions of CAT were higher in diet-exposed worms to Cd as NPs vs soluble form suggesting a specific "nano" effect. Caspase activities increased in worms exposed to soluble Cd and Cd NPs for the two routes of exposure compared to controls. Defences, may be insufficient to prevent reactive oxygen species generation and the associated apoptosis. Behaviour of invertebrates inside sediment showed impairments of body movements in worms exposed to CdS NPs. This study points out oxidative processes as the main consequences of exposure to Cd based NPs in worms. PMID:24480429

  12. Preparation, theory, and biological applications of highly luminescent cadmium selenide/zinc sulfide quantum dots in optical and electron microscopy

    NASA Astrophysics Data System (ADS)

    Bouwer, James Christopher

    This dissertation describes the preparation, theory, and applications of ZnS overcoated CdSe (core) quantum dots for applications as fluorescent probes in optical microscopy and as electron energy loss spectroscopy (EELS) probes in electron microscopy, with applications to the biological sciences. The dissertation begins with a brief overview of quantum dots and their history. Next, a brief overview of the necessary semiconductor theory is discussed including the origin of the band gap, the origin of holes, the concepts of phonons, and trap states. Then, the role of the confinement potential in the quantum dot fluorescent spectrum is discussed in the context of the 3-dimensional spherical well. Included in this discussion is the role of excitonic electron-hole bound states. To provide a complete document useful to anyone who wishes to continue work along these lines, included is a methods section which describes the complete process of synthesis of the CdSe cores, overcoating the cores with ZnS, size selection of nanocrystals, water solubilization, and protein conjugation. The methods used in live cell labeling are included as well. In the section that follows, a discussion of the mathematical methods of image correlation spectroscopy (ICS) for extracting dynamic constants such as flow rates and diffusion constants from time lapse optical image data is discussed in the context of quantum dot fluorescent probes. Dynamic constants were obtained using live NIH3T3 mouse fibroblast cells labeled with IgG-anti-EGF conjugated quantum dots. These same cells were then fixed, imbedded in resin, sectioned to 100nm thick sections and imaged under the electron microscope. The electron dense cadmium selinide provides the contrast necessary to perform direct imaging of EGF receptor sites. In order to improve the data and move toward multi-channel imaging in the electron microscope, EELS spectroscopy and elemental mapping of quantum dots was performed. The theory along with a

  13. Process for removing cadmium from scrap metal

    DOEpatents

    Kronberg, J.W.

    1995-04-11

    A process is described for the recovery of a metal, in particular, cadmium contained in scrap, in a stable form. The process comprises the steps of mixing the cadmium-containing scrap with an ammonium carbonate solution, preferably at least a stoichiometric amount of ammonium carbonate, and/or free ammonia, and an oxidizing agent to form a first mixture so that the cadmium will react with the ammonium carbonate to form a water-soluble ammine complex; evaporating the first mixture so that ammine complex dissociates from the first mixture leaving carbonate ions to react with the cadmium and form a second mixture that includes cadmium carbonate; optionally adding water to the second mixture to form a third mixture; adjusting the pH of the third mixture to the acid range whereby the cadmium carbonate will dissolve; and adding at least a stoichiometric amount of sulfide, preferably in the form of hydrogen sulfide or an aqueous ammonium sulfide solution, to the third mixture to precipitate cadmium sulfide. This mixture of sulfide is then preferably digested by heating to facilitate precipitation of large particles of cadmium sulfide. The scrap may be divided by shredding or breaking up to expose additional surface area. Finally, the precipitated cadmium sulfide can be mixed with glass formers and vitrified for permanent disposal. 2 figures.

  14. Process for removing cadmium from scrap metal

    DOEpatents

    Kronberg, James W.

    1995-01-01

    A process for the recovery of a metal, in particular, cadmium contained in scrap, in a stable form. The process comprises the steps of mixing the cadmium-containing scrap with an ammonium carbonate solution, preferably at least a stoichiometric amount of ammonium carbonate, and/or free ammonia, and an oxidizing agent to form a first mixture so that the cadmium will react with the ammonium carbonate to form a water-soluble ammine complex; evaporating the first mixture so that ammine complex dissociates from the first mixture leaving carbonate ions to react with the cadmium and form a second mixture that includes cadmium carbonate; optionally adding water to the second mixture to form a third mixture; adjusting the pH of the third mixture to the acid range whereby the cadmium carbonate will dissolve; and adding at least a stoichiometric amount of sulfide, preferably in the form of hydrogen sulfide or an aqueous ammonium sulfide solution, to the third mixture to precipitate cadmium sulfide. This mixture of sulfide is then preferably digested by heating to facilitate precipitation of large particles of cadmium sulfide. The scrap may be divided by shredding or breaking up to expose additional surface area. Finally, the precipitated cadmium sulfide can be mixed with glass formers and vitrified for permanent disposal.

  15. Process for removing cadmium from scrap metal

    DOEpatents

    Kronberg, J.W.

    1994-01-01

    A process for the recovery of a metal, in particular, cadmium contained in scrap, in a stable form. The process comprises the steps of mixing the cadmium-containing scrap with an ammonium carbonate solution, preferably at least a stoichiometric amount of ammonium carbonate, and/or free ammonia, and an oxidizing agent to form a first mixture so that the cadmium will react with the ammonium carbonate to form a water-soluble ammine complex; evaporating the first mixture so that ammine complex dissociates from the first mixture leaving carbonate ions to react with the cadmium and form a second mixture that includes cadmium carbonate; optionally adding water to the second mixture to form a third mixture; adjusting the pH of the third mixture to the acid range whereby the cadmium carbonate will dissolve; and adding at least a stoichiometric amount of sulfide, preferably in the form of hydrogen sulfide or an aqueous ammonium sulfide solution, to the third mixture to precipitate cadmium sulfide. This mixture of sulfide is then preferably digested by heating to facilitate precipitation of large particles of cadmium sulfide. The scrap may be divided by shredding or breaking up to exposure additional surface area. Finally, the precipitated cadmium sulfide can be mixed with glass formers and vitrified for permanent disposal.

  16. Thin film cadmium telluride solar cells. Technical progress report No. 2, October 1-December 31, 1979

    SciTech Connect

    Chu, T.L.

    1980-01-01

    The objectives of this contract are to investigate thin films of cadmium telluride on low cost substrates and to demonstrate the feasibility of producing thin film cells with a conversion efficiency of 10% or higher. The chemical vapor deposition of cadmium telluride films on foreign substrates by the direct combination of the elements has been further investigated. Inert substrates such as graphite and tungsten/graphite are not suitable for the deposition of device quality cadmium telluride films because of the rectifying interface and pinhole problems. Indium coated W/graphite forms an ohmic contact with n-type cadmium telluride, and the deposited films are essentially free of pinholes. The properties of Ag/n-CdTe/In/W/graphite structures, such as the current-voltage characteristics as a function of temperature, the barrier height, the photovoltaic properties, and the intragrain diffusion length in cadmium telluride, have been investigated. Preliminary work has also been carried out on the deposition of p-type cadmium telluride films on Sb/W/graphite substrates. The reaction between cadmium iodide and tellurium in a hydrogen atmosphere has been concluded to be unsuitable for the deposition of cadmium telluride films.

  17. Polycrystalline thin film cadmium telluride solar cells fabricated by electrodeposition. Annual subcontract report, 20 March 1993--19 March 1994

    SciTech Connect

    Trefny, J.U.; Furtak, T.E.; Williamson, D.L.; Kim, D.

    1994-07-01

    This report describes the principal results of work performed during the second year of a 3-year program at the Colorado School of Mines (CSM). The work on transparent conducting oxides was carried out primarily by CSM students at NREL and is described in three publications listed in Appendix C. The high-quality ZnO produced from the work was incorporated into a copper indium diselenide cell that exhibited a world-record efficiency of 16.4%. Much of the time was devoted to the improvement of cadmium sulfide films deposited by chemical bath deposition methods and annealed with or without a cadmium chloride treatment. Progress was also made in the electrochemical deposition of cadmium telluride. High-quality films yielding CdS/CdTe/Au cells of greater than 10% efficiency are now being produced on a regular basis. We explored the use of zinc telluride back contacts to form an n-i-p cell structure as previously used by Ametek. We began small-angle x-ray scattering (SAXS) studies to characterize crystal structures, residual stresses, and microstructures of both CdTe and CdS. Large SAXS signals were observed in CdS, most likely because of scattering from gain boundaries. The signals observed to date from CdTe are much weaker, indicating a more homogeneous microstructure. We began to use the ADEPT modeling program, developed at Purdue University, to guide our understanding of the CdS/CdTe cell physics and the improvements that will most likely lead to significantly enhanced efficiencies.

  18. Radiation resistance of thin-film solar cells for space photovoltaic power

    NASA Technical Reports Server (NTRS)

    Woodyard, James R.; Landis, Geoffrey A.

    1991-01-01

    Copper indium diselenide, cadmium telluride, and amorphous silicon alloy solar cells have achieved noteworthy performance and are currently being studied for space power applications. Cadmium sulfide cells had been the subject of much effort but are no longer considered for space applications. A review is presented of what is known about the radiation degradation of thin film solar cells in space. Experimental cadmium telluride and amorphous silicon alloy cells are reviewed. Damage mechanisms and radiation induced defect generation and passivation in the amorphous silicon alloy cell are discussed in detail due to the greater amount of experimental data available.

  19. A metal sulfide photocatalyst composed of ubiquitous elements for solar hydrogen production.

    PubMed

    Shiga, Y; Umezawa, N; Srinivasan, N; Koyasu, S; Sakai, E; Miyauchi, M

    2016-06-14

    A visible-light-sensitive tin sulfide photocatalyst was designed based on a ubiquitous element strategy and density functional theory (DFT) calculations. Computational analysis suggested that tin monosulfide (SnS) would be more efficient than SnS2 as a photocathode for hydrogen production because of the low ionization potential and weak ionic character of SnS. To test this experimentally, nanoparticles of SnS were loaded onto a mesoporous electrode using a wet chemical method, and the bandgap of the synthesized SnS quantum dots was found to be tunable by adjusting the number of successive ionic layer adsorption and reaction (SILAR) cycles, which controls the magnitude of the quantum confinement effect. Efficient hydrogen production was achieved when the bandgap of SnS was wider than that of the bulk form.

  20. Tungsten sulfide enhancing solar-driven hydrogen production from silicon nanowires.

    PubMed

    Huang, Zhipeng; Wang, Chifang; Chen, Zhibo; Meng, Hua; Lv, Cuncai; Chen, Zhongzhong; Han, Ruqu; Zhang, Chi

    2014-07-01

    Tungsten sulfides, including WS2 (crystalline) and WS3 (amorphous), were introduced to silicon nanowires, and both can promote the photoelectrochemical hydrogen production of silicon nanowires. In addition, more enhancement of energy conversion efficiency can be achieved by the loading of WS3, in comparison with loading of WS2. Polarization curves of WS3 and WS2 suggest that WS3 has higher catalytic activity in the hydrogen evolution reaction than WS2, affording higher energy conversion efficiency in silicon nanowires decorated with WS3. The higher electrocatalytic activity of WS3 correlates with the amorphous structure of WS3 and larger surface area of WS3, which result in more active sites in comparison with crystalline WS2.

  1. Solution-grown cadium sulfide films for photovoltaic devices

    SciTech Connect

    Chu, T.L.; Chu, S.S. ); Schultz, N.; Wang, C.; Wu, C.Q. . Dept. of Electrical Engineering)

    1992-09-01

    This paper reports on thin films of cadmium sulfide (CdS) which have major applications in optoelectronic devices. Several techniques have been developed for the deposition of CdS films. Among these, growth of CdS films from an aqueous solution is the low-cost technique suitable for many applications. In this work, the deposition of device quality CdS films on glass and SnO[sub 2]:F/glass substrates from an aqueous solution containing cadmium acetate, ammonia, ammonium acetate, and thiourea has been investigated. The structural and electrical properties of CdS films have been characterized. The doping of CdS films with boron and the properties of boron-doped CdS films have also been studied. High efficiency thin film CdS/CdTe solar cells have been prepared from solution-grown CdS films.

  2. Space-based solar power conversion and delivery systems study. Volume 4: Energy conversion systems studies

    NASA Technical Reports Server (NTRS)

    1977-01-01

    Solar cells and optical configurations for the SSPS were examined. In this task, three specific solar cell materials were examined: single crystal silicon, single crystal gallium arsenide, and polycrystalline cadmium sulfide. The comparison of the three different cells on the basis of a subsystem parametric cost per kW of SSPS-generated power at the terrestrial utility interface showed that gallium arsenide was the most promising solar cell material at high concentration ratios. The most promising solar cell material with no concentration, was dependent upon the particular combination of parameters representing cost, mass and performance that were chosen to represent each cell in this deterministic comparative analysis. The potential for mass production, based on the projections of the present state-of-the-art would tend to favor cadmium sulfide in lieu of single crystal silicon or gallium arsenide solar cells.

  3. Highly effective nickel sulfide counter electrode catalyst prepared by optimal hydrothermal treatment for quantum dot-sensitized solar cells

    NASA Astrophysics Data System (ADS)

    Gopi, Chandu V. V. M.; Srinivasa Rao, S.; Kim, Soo-Kyoung; Punnoose, Dinah; Kim, Hee-Je

    2015-02-01

    Nickel sulfide (NiS) thin film has been deposited on a fluorine-doped tin oxide substrate by a hydrothermal method using 3-mercaptopropionic acid and used as an efficient counter electrode (CE) for polysulfide redox reactions in quantum dot-sensitized solar cells (QDSSCs). NiS has low toxicity and environmental compatibility. In the present study, the size of the NiS nanoparticle increases with the hydrothermal deposition time. The performance of the QDSSCs is examined in detail using polysulfide electrolyte with the NiS CE. A TiO2/CdS/CdSe/ZnS-based QDSSC using the NiS CE shows enhanced photovoltaic performance with a power conversion efficiency (PCE) of 3.03%, which is superior to that of a cell with Pt CE (PCE 2.20%) under one sun illumination (AM 1.5, 100 mW cm-2). The improved photovoltaic performance of the NiS-based QDSSC may be attributed to a low charge transfer resistance (5.08 Ω) for the reduction of polysulfide on the CE, indicating greater electrocatalytic activity of the NiS. Electrochemical impedance spectroscopy, cyclic voltammetry, and Tafel-polarization measurements were used to investigate the electrocatalytic activity of the NiS and Pt CEs.

  4. Batch slurry photocatalytic reactors for the generation of hydrogen from sulfide and sulfite waste streams under solar irradiation

    SciTech Connect

    Priya, R.; Kanmani, S.

    2009-10-15

    In this study, two solar slurry photocatalytic reactors i.e., batch reactor (BR) and batch recycle reactor with continuous supply of inert gas (BRRwCG) were developed for comparing their performance. The performance of the photocatalytic reactors were evaluated based on the generation of hydrogen (H{sub 2}) from water containing sodium sulfide (Na{sub 2}S) and sodium sulfite (Na{sub 2}SO{sub 3}) ions. The photoreactor of capacity 300 mL was developed with UV-vis transparent walls. The catalytic powders ((CdS/ZnS)/Ag{sub 2}S + (RuO{sub 2}/TiO{sub 2})) were kept suspended by means of magnetic stirrer in the BR and gas bubbling and recycling of the suspension in the BRRwCG. The rate constant was found to be 120.86 (einstein{sup -1}) for the BRRwCG whereas, for the BR it was found to be only 10.92 (einstein{sup -1}). The higher rate constant was due to the fast desorption of products and suppression of e{sup -}/h{sup +} recombination. (author)

  5. Titanium dioxide/zinc indium sulfide hetero-junction: An efficient photoanode for the dye-sensitized solar cell

    NASA Astrophysics Data System (ADS)

    Hou, Wenjing; Xiao, Yaoming; Han, Gaoyi; Zhang, Ying; Chang, Yunzhen

    2016-10-01

    A facile strategy is developed for the fabrication of titanium dioxide/zinc indium sulfide (TiO2/ZnIn2S4) hetero-junction photoanode with an adjustable ZnIn2S4 doping content and application in the dye-sensitized solar cell (DSSC). Comparing to the pure TiO2, TiO2/ZnIn2S4 hetero-junction materials demonstrate an enhanced light utilizing efficiency, a reduced recombination rate of electron-hole pairs, and an accelerated migration process of photoinduced electrons. Due to above merits, DSSC based on TiO2/ZnIn2S4 hetero-junction photoanode achieves a greatly enhanced short-circuit current density, leading to an improved photoelectric conversion efficiency of 8.09% under full sunlight illumination (100 mW cm-2, AM 1.5 G), which is almost 14.43% higher than that of the pure TiO2-based DSSC (7.07%).

  6. Efficient Nickel Sulfide and Graphene Counter Electrodes Decorated with Silver Nanoparticles and Application in Dye-Sensitized Solar Cells.

    PubMed

    Yue, Gentian; Li, Fumin; Yang, Guang; Zhang, Weifeng

    2016-12-01

    We reported a facile two-step electrochemical-chemical approach for in situ growth of nickel sulfide and graphene counter electrode (CE) decorated with silver nanoparticles (signed NiS/Gr-Ag) and served in dye-sensitized solar cells (DSSCs). Under optimum conditions, the DSSC achieved a remarkable power conversion efficiency of 8.36 % assembled with the NiS/Gr-Ag CE, much higher than that based on the Pt CE (7.76 %). The surface morphology of NiS/Gr-Ag CE exhibited a smooth surface with cross-growth of NiS, graphene, and Ag nanoparticles, which was beneficial to the fast mass transport of electrolytes; increased the contact area of electrolytes and active materials; and enabled to speed up the reduction of triiodide to iodide. The research on the electrochemical properties also showed that the NiS/Gr-Ag CE possessed lower charge transfer resistance and more excellent electrocatalytic activity in iodide/triiodide electrolyte compared to the Pt electrode.

  7. Efficient Nickel Sulfide and Graphene Counter Electrodes Decorated with Silver Nanoparticles and Application in Dye-Sensitized Solar Cells

    NASA Astrophysics Data System (ADS)

    Yue, Gentian; Li, Fumin; Yang, Guang; Zhang, Weifeng

    2016-05-01

    We reported a facile two-step electrochemical-chemical approach for in situ growth of nickel sulfide and graphene counter electrode (CE) decorated with silver nanoparticles (signed NiS/Gr-Ag) and served in dye-sensitized solar cells (DSSCs). Under optimum conditions, the DSSC achieved a remarkable power conversion efficiency of 8.36 % assembled with the NiS/Gr-Ag CE, much higher than that based on the Pt CE (7.76 %). The surface morphology of NiS/Gr-Ag CE exhibited a smooth surface with cross-growth of NiS, graphene, and Ag nanoparticles, which was beneficial to the fast mass transport of electrolytes; increased the contact area of electrolytes and active materials; and enabled to speed up the reduction of triiodide to iodide. The research on the electrochemical properties also showed that the NiS/Gr-Ag CE possessed lower charge transfer resistance and more excellent electrocatalytic activity in iodide/triiodide electrolyte compared to the Pt electrode.

  8. Green synthesis of wurtzite copper zinc tin sulfide nanocones for improved solar photovoltaic utilization

    NASA Astrophysics Data System (ADS)

    Arora, Leena; Gupta, Poonam; Chhikara, Nitu; Singh, Om Pal; Muhunthan, N.; Singh, V. N.; Singh, B. P.; Jain, Kiran; Chand, S.

    2015-02-01

    Cu2ZnSnS4 (CZTS) is considered to be one of the most promising light absorbing materials for low-cost and high-efficiency thin-film solar cells. It is composed of earth abundant, non-toxic elements. In the present study, wurtzite CZTS nanocone has been synthesized by a green chemistry route. The nanocones have been characterized for its optical, structural and microstructural properties using UV-Vis spectrophotometer, X-ray diffraction, Raman spectroscopy and high-resolution transmission electron microscopy. Optical absorption result shows a band gap of 1.42 eV. XRD and Raman results show wurtzite structure and TEM studies reveal the nanocone structure of the grown material. Growing vertically aligned nanocone structure having smaller diameter shall help in enhancing the light absorption in broader range which shall enhance the efficiency of solar cell. This study is a step in this direction.

  9. The 100 kW space station. [regenerative fuel cells and nickel hydrogen and nickel cadmium batteries for solar arrays

    NASA Technical Reports Server (NTRS)

    Mckhann, G.

    1977-01-01

    Solar array power systems for the space construction base are discussed. Nickel cadmium and nickel hydrogen batteries are equally attractive relative to regenerative fuel cell systems at 5 years life. Further evaluation of energy storage system life (low orbit conditions) is required. Shuttle and solid polymer electrolyte fuel cell technology appears adequate; large units (approximately four times shuttle) are most appropriate and should be studied for a 100 KWe SCB system. A conservative NiH2 battery DOD (18.6%) was elected due to lack of test data and offers considerable improvement potential. Multiorbit load averaging and reserve capacity requirements limit nominal DOD to 30% to 50% maximum, independent of life considerations.

  10. Indium phosphide/cadmium sulfide thin-film solar cells. Final report, May 1979 through July 1980

    SciTech Connect

    Zanio, K.

    1980-09-01

    Thin-film InP/RXCdS/ITO/GLASS devices were prepared by depositing ITO on low-cost glass substrate, depositing CdS on the ITO by thermal evaporation, increasing the CdS lateral grain size by recrystallization, and depositing p-type InP by planar reactive deposition (PRD) on the recrystallized CdS (RXCdS). Yields of the RXCdS/ITO/GLASS substrates were increased to 90% with lateral dimensions of the RXCdS grains as large as 0.3 mm. P-type InP layers were obtained with Be doping. S-doping via vapor transport from the CdS was eliminated by capping the entire RXCdS substrate with InP. For InP deposited on RXCdS at 380/sup 0/C, devices showed blocking action with a barrier height of about 0.5 V but no light response, possibly due to an intermediate approx. 3-..mu..m-thick n-InP layer from diffusion of S from the RXCdS. These results were achieved despite poor InP epitaxy due to an approx. 0.5-..mu..m-thick In-Cd-S transition layer between the InP and the RXCdS. InP films were subsequently deposited on RXCdS at the reduced substrate temperature of 280/sup 0/C to reduce S-diffusion and improve the quality of the epitaxy. Complete InP epitaxy on RXCdS was achieved with the lateral dimensions of the InP (approx. = 40 ..mu..m) replicating that of the RXCdS. Given the increase in the concentration of n-type native defects as substrate temperature is decreased, the present lower limit for obtaining p-type InP by vacuum technologies appears to be about 300/sup 0/C. A 300 to 350/sup 0/C range of substrate temperature appears to befeasible for preparing large-grained p-type InP for both frontwall and backwall cell. However, if the thickness of the n-type layer due to S diffusion cannot be kept to less than a few thousand Angstroms, then development must be restricted to the frontwall cells.

  11. Indium phosphide/cadmium sulfide thin-film solar cells. Quarterly technical progress report No. 3, December 1979-April 1980

    SciTech Connect

    Zanio, K.

    1980-06-01

    Thin films (approx. 1 ..mu..m thick) and large grains (approx. 40 x 40 ..mu..m) of InP were epitaxially deposited on low-cost recrystallized CdS (RXCdS) substrates at 280/sup 0/C by planar reactive deposition. At 380/sup 0/C, a 0.4- to 1.0-..mu..m-thick In-Cd-S transition layer between the InP and the RXCdS degrades the quality of the InP epitaxy. However, p-type InP films were prepared at this temperature by Be-doping and capping the entire RXCdS substrate with InP. Large grains of CdTe (approx. 40 ..mu..m) were also deposited on RXCdS substrates at 460/sup 0/C by physical vapor deposition. The grain size of the RXCdS is typically 40 ..mu..m. However, during this period we prepared RXCdS with grains having dimensions up to 300 ..mu..m.

  12. Graphene assistance enhanced dye-sensitized solar cell performance of tin sulfide microspheres

    NASA Astrophysics Data System (ADS)

    Yang, Bo; Chen, Peng; Zuo, Xueqin; Zhou, Lei; Yang, Xiao; Li, Guang; Wu, Mingzai; Ma, Yongqing; Jin, Shaowei; Zhu, Kerong

    2015-10-01

    In this work, the nanosheet-assembled SnS2 microspheres were synthesized through a solvothermal method, and the catalytic activities of the microspheres were investigated by J-V and power conversion efficiency tests as counter electrodes in dye-sensitized solar cells. The cell showed an energy conversion efficiency up to 6.4%. To further improve the power conversion efficiency of the counter electrode of the microspheres, different amounts of reduced graphene were added into the microspheres by simply physical mixing. With the addition of 6 wt% reduced graphene, the short-circuit current density, open-circuit voltage and fill factor were 15.18 mA cm-2, 775 mV, and 63.4%, respectively. More important, the conversion efficiency reached 7.46%, which is approximately 17% higher than that of the cell with pure SnS2 microspheres as counter electrode. Compared to conventional materials used in dye-sensitized solar cells, SnS2 microspheres have the advantages of facile synthesis, low-cost and high efficiency with graphene assistance.

  13. Lead sulfide nanocrystal quantum dot solar cells with trenched ZnO fabricated via nanoimprinting.

    PubMed

    Kim, Sarah; Kim, Jun Kwan; Gao, Jianbo; Song, Jung Hoon; An, Hey Jin; You, Tae-Soo; Lee, Tae-Soo; Jeong, Jong-Ryul; Lee, Eung-Sug; Jeong, Jun-Ho; Beard, Matthew C; Jeong, Sohee

    2013-05-01

    The improvement of power conversion efficiency, especially current density (Jsc), for nanocrystal quantum dot based heterojunction solar cells was realized by employing a trenched ZnO film fabricated using nanoimprint techniques. For an optimization of ZnO patterns, various patterned ZnO films were investigated using electrical and optical analysis methods by varying the line width, interpattern distance, pattern height, and residual layer. Analyzing the features of patterned ZnO films allowed us to simultaneously optimize both the pronounced electrical effects as well as optical properties. Consequently, we achieved an enhancement in Jsc from 7.82 to 12.5 mA cm(-2) by adopting the patterned ZnO with optimized trenched shape.

  14. Study of copper sulfide counter electrode on the performances of CdS/CdSe/ZnS-sensitized hierarchical TiO2 spheres quantum dots solar cells

    NASA Astrophysics Data System (ADS)

    Buatong, Nattha; Tang, I.-Ming; Pon-On, Weeraphat

    2015-07-01

    The effects of using copper sulfide (CuS) counter electrodes on the performances of solar cells made with CdS/CdSe/ZnS quantum dots co-sensitized onto hierarchical TiO2 spheres (HTS) used as photoelectrode is reported. The HTS in the QDSSCs is composed of an assembly of numerous TiO2 spheres made by the solvolthermal method. The photoelectrical performance of HTS/CdS/CdSe/ZnS coupled to CuS counter electrode was compared to those coupled to Pt CE. The HTS/CdS/CdSe/ZnS coupled to the CuS CE showed the highest power conversion efficiency η (of 1.310 %.) which is significantly higher than those using a standard Pt CE (η = 0.374%) (3.50 fold). This higher efficiency is the results of the higher electrocatalytic activities when the copper sulfide CEs is used.

  15. PVD of copper sulfide (Cu2S) for PIN-structured solar cells

    NASA Astrophysics Data System (ADS)

    Siol, Sebastian; Sträter, Hendrik; Brüggemann, Rudolf; Brötz, Joachim; Bauer, Gottfried H.; Klein, Andreas; Jaegermann, Wolfram

    2013-12-01

    Thin layers of chalcocite (Cu2S) have been deposited via physical vapour deposition using various pre- and post-treatment parameters. The electrical and morphological properties have been investigated by in situ XPS, SEM and XRD measurements. Calibrated photoluminescence experiments were performed to investigate the material's suitability as an absorber layer in thin-film solar cells. Measurements of annealed Cu2S layers on glass without any surface passivation showed an optical band gap of 1.25 eV as well as a splitting of the quasi-Fermi levels of 710 meV. This value exceeds the highest reported open-circuit voltage for Cu2S-based devices so far, which leads to the assumption that Cu2S has not been brought to its full potential yet. The band alignments for ZnO/Cu2S as well as Cu2S/Cu2O interfaces have been determined using in situ XPS interface experiments to suggest a novel device structure according to the favourable PIN-layout. First devices have been built, but show no efficiency due to shunting caused by the inferior morphology of the absorber layers.

  16. Concentrations of carbonyl sulfide and hydrogen cyanide in the free upper troposphere and lower stratosphere deduced from ATMOS/Spacelab 3 infrared solar occultation spectra

    NASA Technical Reports Server (NTRS)

    Zander, R.; Rinsland, C. P.; Russell, J. M., III; Farmer, C. B.; Norton, R. H.

    1988-01-01

    This paper presents the results on the volume mixing ratio profiles of carbonyl sulfide and hydrogen cyanide, deduced from the spectroscopic analysis of IR solar absorption spectra obtained in the occultation mode with the Atmospheric Trace Molecule Spectroscopy (ATMOS) instrument during its mission aboard Spacelab 3. A comparison of the ATMOS measurements for both northern and southern latitudes with previous field investigations at low midlatitudes shows a relatively good agreement. Southern Hemisphere volume mixing ratio profiles for both molecules were obtained for the first time, as were the profiles for the Northern Hemisphere covering the upper troposphere and the lower stratosphere simultaneously.

  17. The role of acid-volatile sulfide and interstitial water metal concentrations in determining bioavailability of cadmium and nickel from contaminated sediments to the marine polychaete Neanthes arenaceodentata

    SciTech Connect

    Pesch, C.E.; Hansen, D.J.; Boothman, W.S. . Environmental Research Lab.); Berry, W.J. ); Mahony, J.D. . Chemistry Dept.)

    1995-01-01

    This study investigated the influence of acid-volatile sulfide (AVS) and interstitial water (IW) metal concentrations on bioavailability and toxicity of Cd and Ni to an infaunal sediment-ingesting marine worm, Neanthes Arenaceodentata. Ten-d exposures were conducted with sediments, contaminated primarily with Cd and Ni, from Foundry Cove (Hudson River, NY), and with uncontaminated sediments spiked with Cd or Ni. Molar ratios of simultaneously extracted metal (SEM)/AVS ranged from < 0.02 to 44 for Cd-spiked, 0.02 to 241 for Ni-spiked, and <0.06 to 125 for Foundry Cove sediments. In all experiments, significant mortality was not observed when SEM/AVS ratios were <1.0 and interstitial water toxic units (IWTU) were <1.0. In the Cd and Ni-spiked experiments, when SEM/AVS ratios or IWTUs were >1.0, sediments were either lethal or worms did not burrow. Mortality of worms in Foundry Cove sediments was [le] 20%, and worms burrowed in all these sediments. However, IW contained <1.0 TU (Ni + Cd) in all Foundry Cove sediments except one (IWTU = 1.69). Metal concentrations in worms generally increased with increases in sediment metal concentration, SEM/AVS molar ratio, and IW metal concentration. The presence of metal in worms from sediments from SEM/AVS ratios <1.0 may be evidence of release of Cd or Ni from oxidized metal sulfide (a result of burrowing), uptake of metal from ingested sediment, or adsorption to body surfaces. These results support the hypothesis that when the concentration of AVS in sediments exceeds that of divalent metals sediments will not be acutely toxic. However, a greater number of sediments was correctly predicted to be nontoxic when interstitial water metal concentration of <1.0 TU was used.

  18. Solar electric and thermal conversion system in close proximity to the consumer. [solar panels on house roofs

    NASA Technical Reports Server (NTRS)

    Boeer, K. W.

    1975-01-01

    Solar cells may be used to convert sunlight directly into electrical energy and into lowgrade heat to be used for large-scale terrestrial solar-energy conversion. Both forms of energy can be utilized if such cells are deployed in close proximity to the consumer (rooftop). Cadmium-sulfide/copper-sulfide (CdS/Cu2S) solar cells are an example of cells which may be produced inexpensively enough to become economically attractive. Cell parameters relevant for combined solar conversion are presented. Critical issues, such as production yield, life expectancy, and stability of performance, are discussed. Systems-design parameters related to operating temperatures are analyzed. First results obtained on Solar One, the experimental house of the University of Delaware, are given. Economic aspects are discussed. Different modes of operation are discussed in respect to the power utility and consumer incentives.

  19. Determination of Hydrogen Sulfide in Fermentation Broths Containing SO21

    PubMed Central

    Acree, T. E.; Sonoff, Elisabeth P.; Splittstoesser, D. F.

    1971-01-01

    A procedure for the determination of hydrogen sulfide in fermentation broths containing up to 100 μg of SO2 per ml is described. The method involves the sparging of H2S from the broth into a cadmium hydroxide absorption solution, the formation of methylene blue from the absorbed sulfide, and the measuring of this color spectrophotometrically. The use of cadmium hydroxide instead of zinc acetate, the common absorbent, substantially reduced the interference of SO2 with the analysis. PMID:5111300

  20. Platinum-Free Counter Electrode Comprised of Metal-Organic-Framework (MOF)-Derived Cobalt Sulfide Nanoparticles for Efficient Dye-Sensitized Solar Cells (DSSCs)

    PubMed Central

    Hsu, Shao-Hui; Li, Chun-Ting; Chien, Heng-Ta; Salunkhe, Rahul R.; Suzuki, Norihiro; Yamauchi, Yusuke; Ho, Kuo-Chuan; Wu, Kevin C.-W.

    2014-01-01

    We fabricated a highly efficient (with a solar-to-electricity conversion efficiency (η) of 8.1%) Pt-free dye-sensitized solar cell (DSSC). The counter electrode was made of cobalt sulfide (CoS) nanoparticles synthesized via surfactant-assisted preparation of a metal organic framework, ZIF-67, with controllable particle sizes (50 to 320 nm) and subsequent oxidation and sulfide conversion. In contrast to conventional Pt counter electrodes, the synthesized CoS nanoparticles exhibited higher external surface areas and roughness factors, as evidenced by X-ray diffraction (XRD), scanning electron microscopy (SEM) element mapping, and electrochemical analysis. Incident photon-to-current conversion efficiency (IPCE) results showed an increase in the open circuit voltage (VOC) and a decrease in the short-circuit photocurrent density (Jsc) for CoS-based DSSCs compared to Pt-based DSSCs, resulting in a similar power conversion efficiency. The CoS-based DSSC fabricated in the study show great potential for economically friendly production of Pt-free DSSCs. PMID:25382139

  1. High efficiency cadmium and zinc telluride-based thin film solar cells

    SciTech Connect

    Rohatgi, A.; Summers, C.J.; Erbil, A.; Sudharsanan, R.; Ringel, S. . School of Electrical Engineering)

    1990-10-01

    Polycrystalline Cd{sub 1-x}Zn{sub x}Te and Cd{sub 1-x}Mn{sub x}Te films with a band gap of 1.7 eV were successfully grown on glass/SnO{sub 2}/CdS substrates by molecular beam epitaxy (MBE) and metal-organic chemical vapor deposition (MOCVD), respectively. Polycrystalline Cd{sub 1-x}Zn{sub x}Te films grown by MBE resulted in uniform composition and sharp interfaces. However, polycrystalline Cd{sub 1-x}Mn{sub x}Te films grown by MOCVD showed nonuniform compositions and evidence of manganese accumulation at the Cd{sub 1-x}Mn{sub x}Te/CdS interface. We found that manganese interdiffuses and replaces cadmium in the CdS film. By improving the CdTe/CdS interface and, thus, reducing the collection function effects, the efficiency of the MOCVD CdTe cell can be improved to about 13.5%. MBE-grown CdTe cells also produced 8%--9% efficiencies. The standard CdTe process was not optimum for ternary films and resulted in a decrease in the band gap. Recent results indicate that CdCl{sub 2} + ZnCl{sub 2} chemical treatment may prevent the band-gap reduction, and that chromate etch (rather than bromine etch) may provide the solution to contact resistance in the ternary cells.

  2. Selenium Sulfide

    MedlinePlus

    Selenium sulfide comes in a lotion and is usually applied as a shampoo. As a shampoo, selenium sulfide usually is used twice a week for the first ... it is irritating. Rinse off all of the lotion.Do not use this medication on children younger ...

  3. Electron-reflector strategy for cadmium telluride thin-film solar cells

    NASA Astrophysics Data System (ADS)

    Hsiao, Kuo-Jui

    The CdTe thin-film solar cell has a large absorption coefficient and high theoretical efficiency. Moreover, large-area photovoltaic panels can be economically fabricated. These features potentially make the CdTe thin-film solar cell the leading alternative energy source. However, the record CdTe efficiency (16.5%) is much less than its theoretical maximum efficiency (29%), primarily because the open-circuit voltage (0.845 V) is well below what is expected for its band gap (1.5 eV). The incorporation of an electron reflector is a strategy to improve the open-circuit voltage of solar cells, and thus a strong possibility to improve the efficiency of CdTe thin-film solar cells. An electron reflector is a conduction-band energy barrier at the back surface of the solar cell, which can reduce the recombination due to the electron flow to the back surface. Different methods to create an electron reflector are explained in the thesis: (1) expanded band gap, either an expanded-band-gap layer or a bulk-band-gap reduction, and (2) alteration to the band bending through a reversed back barrier or a heavily-doped back surface. Investigation shows that the expanded-band-gap layer is the most efficient and practical mechanism for an electron reflector, and the combination of any two mechanisms does not yield additional improvement. To have the optimal effect from the electron-reflector strategy, reasonable CdTe lifetime (1 ns or above) and full depletion of the CdTe layer are required to ensure high carrier collection. Furthermore, a good-quality reflector interface between the p-type CdTe layer and the electron-reflector layer is essential. Preliminary experimental evidence has shown that CdTe cells with a ZnTe back layer do have a slightly higher open-circuit voltage. An electron reflector should be particularly beneficial for thin (less than 2 microm) CdTe cells which have a fully-depleted CdTe absorber layer. Thin CdTe cells can also benefit from the optical reflection at the

  4. Non-Uniformities in Thin-Film Cadmium Telluride Solar Cells Using Electroluminescence and Photoluminescence: Preprint

    SciTech Connect

    Zaunbrecher, K.; Johnston, S.; Yan, F.; Sites, J.

    2011-07-01

    It is the purpose of this research to develop specific imaging techniques that have the potential to be fast, in-line tools for quality control in thin-film CdTe solar cells. Electroluminescence (EL) and photoluminescence (PL) are two techniques that are currently under investigation on CdTe small area devices made at Colorado State University. It is our hope to significantly advance the understanding of EL and PL measurements as applied to CdTe. Qualitative analysis of defects and non-uniformities is underway on CdTe using EL, PL, and other imaging techniques.

  5. CuxS counter electrodes in-situ prepared via the sulfidation of magnetron sputtering Cu film for quantum dot sensitized solar cells

    NASA Astrophysics Data System (ADS)

    Wang, Yuanqiang; Zhang, Qinghong; Li, Yaogang; Wang, Hongzhi

    2016-06-01

    The nanosheet-structured CuxS thin films used as counter electrodes (CEs) for CdS/CdSe quantum dot sensitized solar cells (QDSSCs) have been in situ prepared via the sulfidation of Cu nanoparticles deposited on F-doped SnO2 glass (FTO glass) substrate by magnetron sputtering method. The thickness of the deposited Cu film affects the morphology and thickness of the obtained CuxS films. The CuxS nanosheet films have good adhesion with FTO glass and the surface exhibits uniform morphology. The characteristics of QDSSCs are studied in more detail by photocurrent-voltage performance measurements, incident photon-to-current conversion efficiency (IPCE) and electrochemical impedance spectroscopy (EIS). The CuxS on FTO glass (CuxS/FTO) CEs show much higher power conversion efficiency (PCE) and IPCE than those of the Pt on FTO (Pt/FTO) CE because of their superior carrier mobility and electro-catalytic ability for the polysulfide redox reactions. Based on an optimal CuxS film thickness of 2.7 μm obtained by the sulfidation of the Cu film thickness of 300 nm on FTO, the best photovoltaic performance with PCE of 3.67% (Jsc = 16.47 mA cm-2, Voc = 0.481 V, FF = 0.46) under full one-sun illumination is achieved.

  6. Study of copper-free back contacts to thin film cadmium telluride solar cells

    NASA Astrophysics Data System (ADS)

    Viswanathan, Vijay

    The goals of this project are to study Cu free back contact alternatives for CdS/CdTe thin film solar cells, and to research dry etching for CdTe surface preparation before contact application. In addition, an attempt has been made to evaluate the stability of some of the contacts researched. The contacts studied in this work include ZnTe/Cu2Te, Sb2Te 3, and Ni-P alloys. The ZnTe/Cu2Te contact system is studied as basically an extension of the earlier work done on Cu2Te at USF. RF sputtering from a compound target of ZnTe and Cu2Te respectively deposits these layers on etched CdTe surface. The effect of Cu2Te thickness and deposition temperature on contact and cell performance will be studied with the ZnTe depositions conditions kept constant. C-V measurements to study the effect of contact deposition conditions on CdTe doping will also be performed. These contacts will then be stressed to high temperatures (70--100°C) and their stability with stress time is analyzed. Sb2Te3 will be deposited on glass using RF sputtering, to study film properties with deposition temperature. The Sb2Te 3 contact performance will also be studied as a function of the Sb 2Te3 deposition temperature and thickness. The suitability of Ni-P alloys for back contacts to CdTe solar cells was studied by forming a colloidal mixture of Ni2P in graphite paste. The Ni-P contacts, painted on Br-methanol etched CdTe surface, will be studied as a function of Ni-P concentration (in the graphite paste), annealing temperature and time. Some of these cells will undergo temperature stress testing to determine contact behavior with time. Dry etching of CdTe will be studied as an alternative for wet etching processes currently used for CdTe solar cells. The CdTe surface is isotropically etched in a barrel reactor in N2, Ar or Ar:O 2 ambient. The effect of etching ambient, pressure, plasma power and etch time on contact performance will be studied.

  7. Cadmium Sulfide and Nickel Synergetic Co-catalysts Supported on Graphitic Carbon Nitride for Visible-Light-Driven Photocatalytic Hydrogen Evolution

    PubMed Central

    Yue, Xinzheng; Yi, Shasha; Wang, Runwei; Zhang, Zongtao; Qiu, Shilun

    2016-01-01

    Design and preparation of noble-metal-free photocatalysts is of great importance for photocatalytic water splitting harvesting solar energy. Here, we report the high visible-light-driven hydrogen evolution upon the hybrid photocatalyst system consisting of CdS nanocrystals and Ni@NiO nanoparticles grown on the surface of g-C3N4. The hybrid system shows a high H2-production rate of 1258.7 μmol h−1 g−1 in the presence of triethanolamine as a sacrificial electron donor under visible light irradiation. The synergetic catalytic mechanism has been studied and the results of photovoltaic and photoluminescence properties show that efficient electron transfer could be achieved from g-C3N4 to CdS nanocrystals and subsequently to Ni@NiO hybrid. PMID:26923439

  8. Cadmium Sulfide and Nickel Synergetic Co-catalysts Supported on Graphitic Carbon Nitride for Visible-Light-Driven Photocatalytic Hydrogen Evolution.

    PubMed

    Yue, Xinzheng; Yi, Shasha; Wang, Runwei; Zhang, Zongtao; Qiu, Shilun

    2016-01-01

    Design and preparation of noble-metal-free photocatalysts is of great importance for photocatalytic water splitting harvesting solar energy. Here, we report the high visible-light-driven hydrogen evolution upon the hybrid photocatalyst system consisting of CdS nanocrystals and Ni@NiO nanoparticles grown on the surface of g-C3N4. The hybrid system shows a high H2-production rate of 1258.7 μmol h(-1) g(-1) in the presence of triethanolamine as a sacrificial electron donor under visible light irradiation. The synergetic catalytic mechanism has been studied and the results of photovoltaic and photoluminescence properties show that efficient electron transfer could be achieved from g-C3N4 to CdS nanocrystals and subsequently to Ni@NiO hybrid. PMID:26923439

  9. Analysis of advanced vapor source for cadmium telluride solar cell manufacturing

    NASA Astrophysics Data System (ADS)

    Khetani, Tejas Harshadkumar

    A thin film CdS/CdTe solar cell manufacturing line has been developed in the Materials Engineering Laboratory at Colorado State University. The original design incorporated infrared lamps for heating the vapor source. This system has been redesigned to improve the energy efficiency of the system, allow co-sublimation and allow longer run time before the sources have to be replenished. The advanced vapor source incorporates conduction heating with heating elements embedded in graphite. The advanced vapor source was modeled by computational fluid dynamics (CFD). From these models, the required maximum operating temperature of the element was determined to be 720 C for the processing of CdS/CdTe solar cells. Nichrome and Kanthal A1 were primarily selected for this application at temperature of 720 °C in vacuum with oxygen partial pressure. Research on oxidation effects and life due to oxidation as well as creep deformation was done, and Nichrome was found more suitable for this application. A study of the life of the Nichrome heating elements in this application was conducted and the estimate of life is approximately 1900 years for repeated on-off application. This is many orders of magnitude higher than the life of infrared heat lamps. Ceramic cement based on aluminum oxide (Resbond 920) is used for bonding the elements to the graphite. Thermodynamic calculations showed that this cement is inert to the heating element. An earlier design of the advanced source encountered failure of the element. The failed element was studies by scanning electron microscopy and the failure was attributed to loss of adhesion between the graphite and the ceramic element. The design has been modified and the advanced vapor source is currently in operation.

  10. Polycrystalline thin-film cadmium telluride solar cells fabricated by electrodeposition. Annual technical report

    SciTech Connect

    Trefny, J.U.; Mao, D.

    1998-01-01

    During the past year, Colorado School of Mines (CSM) researchers performed systematic studies of the growth and properties of electrodeposition CdS and back-contact formation using Cu-doped ZnTe, with an emphasis on low Cu concentrations. CSM also started to explore the stability of its ZnTe-Cu contacted CdTe solar cells. Researchers investigated the electrodeposition of CdS and its application in fabricating CdTe/CdS solar cells. The experimental conditions they explored in this study were pH from 2.0 to 3.0; temperatures of 80 and 90 C; CdCl{sub 2} concentration of 0.2 M; deposition potential from {minus}550 to {minus}600 mV vs. Ag/AgCl electrode; [Na{sub 2}S{sub 2}O{sub 4}] concentration between 0.005 and 0.05 M. The deposition rate increases with increase of the thiosulfate concentration and decrease of solution pH. Researchers also extended their previous research of ZnTe:Cu films by investigating films doped with low Cu concentrations (< 5 at. %). The low Cu concentration enabled them to increase the ZnTe:Cu post-annealing temperature without causing excessive Cu diffusion into CdTe or formation of secondary phases. The effects of Cu doping concentration and post-deposition annealing temperature on the structural, compositional, and electrical properties of ZnTe were studied systematically using X-ray diffraction, atomic force microscopy, electron microprobe, Hall effect, and conductivity measurements.

  11. Radio-frequency magnetron triode sputtering of cadmium telluride and zinc telluride films and solar cells

    NASA Astrophysics Data System (ADS)

    Sanford, Adam Lee

    The n-CdS/p-CdTe solar cell has been researched for many years now. Research groups use a variety of processes to fabricate thin-film CdS/CdTe cells, including physical vapor deposition, chemical vapor deposition, and RF diode sputtering. One of the central areas of investigation concerning CdS/CdTe cells is the problem of a Schottky barrier at the back contact. Even cells fabricated with ohmic back contacts degrade into Schottky barriers as the devices are used. This severely degrades power generation. One possible solution is to use p+-ZnTe as an interlayer between CdTe and the back contact. ZnTe is easily doped with Cu to be p-type. However, even contacts with this ZnTe interlayer degrade over time, because Cu is highly mobile and diffuses away from the contact towards the CdS/CdTe junction. Another possibility is to dope ZnTe with N. It has been demonstrated using molecular beam epitaxy and RF diode sputtering. In this study, CdTe films are fabricated using a variation of RF diode sputtering called triode sputtering. This technique allows for control of ion bombardment to the substrate during deposition. Also, a higher plasma density near the target is achieved allowing depositions at lower pressures. These films are characterized structurally to show the effects of the various deposition parameters. N-doped ZnTe films are also fabricated using this technique. These films are characterized electrically to show the effects of the various deposition parameters. Also, the effects of post-deposition annealing are observed. It is found that annealing at the right temperature can increase the conductivity of the films by a factor of 3 or more. However, annealing at higher temperatures decreases the conductivity to as low as 12% of the initial conductivity. Finally, RF triode sputtered N-doped ZnTe films are used as an interlayer at the back contact of a CdS/CdTe solar cell. The effects of annealing the device before and after contact deposition are observed

  12. Thin film cadmium telluride solar cells. Progress report, 1 October 1983-30 September 1984

    SciTech Connect

    Chu, T.L.

    1985-04-01

    During this reporting period, the deposition of CdTe films by the direct combination of the Cd and Te vapor on foreign substrates has been continued with emphasis on the resistivity control of p-type films and the reduction of p-CdTe/substrate interface resistance. CdTe films deposited on graphite substrates were all p-type, irrespective of the substrate temperature and the reactant composition. This result indicates that carbon is incorporated into CdTe presumably thru its reaction with Te and that carbon is electrically active in CdTe. Using W/graphite as substrates, the change in conductivity type of nearly stoichiometric films has been found to take place over a very narrow range of the reactant composition. In addition to using a Cd-deficient reactant mixture, the resistivity of p-type CdTe films may also be controlled by adding a dopant to the reactant mixture. The effect of reactant composition and substrate temperature on the resistivity of the reactant mixture was studied in detail. The effect of adding oxygen to the reactant was also investigated. Using CdTe films deposited on Corning 7059 glass substrates, the optical band gap of CdTe films was found to be 1.50 eV at room temperature. The preparation and characterization of thin film cadium telluride heterojunction solar cells have been continued. The open-circuit voltage (up to 0.75V) and short-circuit current density (up to 20mA/cm/sup 2/) are reasonably reproducible; however, the high p-CdTe/substrate interface resistance remains to be a problem in the fabrication of thin film CdTe solar cells. Because of the uncontrolled series resistance, the best CdS/CdTe cells have an AM1 efficiency of about 6.5% and the best ITO/CdTe cell has an AM1 efficiency of about 8%. Further work will be directed to the use of inverted structures.

  13. Self-photosensitization of nonphotosynthetic bacteria for solar-to-chemical production.

    PubMed

    Sakimoto, Kelsey K; Wong, Andrew Barnabas; Yang, Peidong

    2016-01-01

    Improving natural photosynthesis can enable the sustainable production of chemicals. However, neither purely artificial nor purely biological approaches seem poised to realize the potential of solar-to-chemical synthesis. We developed a hybrid approach, whereby we combined the highly efficient light harvesting of inorganic semiconductors with the high specificity, low cost, and self-replication and -repair of biocatalysts. We induced the self-photosensitization of a nonphotosynthetic bacterium, Moorella thermoacetica, with cadmium sulfide nanoparticles, enabling the photosynthesis of acetic acid from carbon dioxide. Biologically precipitated cadmium sulfide nanoparticles served as the light harvester to sustain cellular metabolism. This self-augmented biological system selectively produced acetic acid continuously over several days of light-dark cycles at relatively high quantum yields, demonstrating a self-replicating route toward solar-to-chemical carbon dioxide reduction. PMID:26721997

  14. Self-photosensitization of nonphotosynthetic bacteria for solar-to-chemical production.

    PubMed

    Sakimoto, Kelsey K; Wong, Andrew Barnabas; Yang, Peidong

    2016-01-01

    Improving natural photosynthesis can enable the sustainable production of chemicals. However, neither purely artificial nor purely biological approaches seem poised to realize the potential of solar-to-chemical synthesis. We developed a hybrid approach, whereby we combined the highly efficient light harvesting of inorganic semiconductors with the high specificity, low cost, and self-replication and -repair of biocatalysts. We induced the self-photosensitization of a nonphotosynthetic bacterium, Moorella thermoacetica, with cadmium sulfide nanoparticles, enabling the photosynthesis of acetic acid from carbon dioxide. Biologically precipitated cadmium sulfide nanoparticles served as the light harvester to sustain cellular metabolism. This self-augmented biological system selectively produced acetic acid continuously over several days of light-dark cycles at relatively high quantum yields, demonstrating a self-replicating route toward solar-to-chemical carbon dioxide reduction.

  15. Role of the copper-oxygen defect in cadmium telluride solar cells

    NASA Astrophysics Data System (ADS)

    Corwine, Caroline R.

    Thin-film CdTe is one of the leading materials used in photovoltaic (PV) solar cells. One way to improve device performance and stability is through understanding how various device processing steps alter defect states in the CdTe layer. Photoluminescence (PL) studies can be used to examine radiative defects in materials. This study uses low-temperature PL to probe the defects present in thin-film CdTe deposited for solar cells. One key defect seen in the thin-film CdTe was reproduced in single-crystal (sX) CdTe by systematic incorporation of known impurities in the thin-film growth process, hence demonstrating that both copper and oxygen were necessary for its formation. Polycrystalline (pX) thin-film glass/SnO2:F/CdS/CdTe structures were examined. The CdTe layer was grown via close-spaced sublimation (CSS), vapor transport deposition (VTD), and physical vapor deposition (PVD). After CdTe deposition, followed by a standard CdC12 treatment and a ZnTe:Cu back contact, a PL peak was seen at ˜1.46 eV from the free back surface of all samples (1.456 eV for CSS and PVD, 1.460-1.463 eV for VTD). However, before the Cu-containing contact was added, this peak was not seen from the front of the CdTe (the CdS/CdTe junction region) in any device with CdTe thickness greater than 4 mum. The CdCl2 treatment commonly used to increase CdTe grain size did not enhance or reduce the peak at ˜1.46 eV relative to the rest of the PL spectrum. When the Cu-containing contact was applied, the PL spectra from both the front and back of the CdTe exhibited the peak at 1.456 eV. The PL peak at ˜1.46 eV was present in thin-film CdTe after deposition, when the dominant impurities are expected to be both Cu from the CdTe source material and O introduced in the chamber during growth to assist in CdTe film density. Since Cu and/or O appeared to be involved in this defect, PL studies were done with sX CdTe to distinguish between the separate effects of Cu or O and the combined effect of Cu and O

  16. High-efficiency cadmium and zinc-telluride-based thin-film solar cells

    SciTech Connect

    Rohatgi, A.; Sudharsanan, R.; Ringel, S. )

    1992-02-01

    This report describes research into polycrystalline CdTe solar cells grown by metal-organic chemical vapor deposition. Efficiencies of {approximately}10% were achieved using both p-i-n and p-n structures. A pre-heat treatment of CdS/SnO{sub 2}/glass substrates at 450{degrees}C in hydrogen atmosphere prior to the CdTe growth was found to be essential for high performance because this heat treatment reduces oxygen-related defects from the CdS surface. However, this treatment also resulted in a Cd-deficient CdS surface, which may in part limit the CdTe cell efficiency to 10% due to Cd vacancy-related interface defects. Preliminary model calculations suggest that removing these states can increase the cell efficiency from 10% to 13.5%. Photon absorption in the CdS film also limits the cell performance, and eliminating this loss mechanism can result in CdTe efficiencies in excess of 18%. Polycrystalline, 1.7-e, CdZnTe films were also grown for tandem-cell applications. CdZnTe/CdS cells processed using the standard CdTe cell fabrication procedure resulted in 4.4% efficiency, high series resistance, and a band-gap shift to 1.55 eV. The formation of Zn-O at and near the CdZnTe surface is the source of high contact resistance. A saturated dichromate each prior to contact deposition was found to solve the contact resistance problem. The CdCl{sub 2} treatment was identified as the cause of the observed band-gap shift due to the preferred formation of ZnCl{sub 2}. 59 refs.

  17. a Study of Deep Levels in COPPER-INDIUM-SELENIUM(2) by Current-Voltage Capacitance-Voltage and Capacitance Transient Measurements on Cadmium-Sulfide -SELENIUM(2)

    NASA Astrophysics Data System (ADS)

    Christoforou, Nicholas

    A study was made of the deep levels in CuInSe _ 2 thin films by Current-Voltage, Capacitance-Voltage, Capacitance-Temperature, and Capacitance Transient measurements on CdS/CuInSe_ 2 solar cells. To accomplish this study, a semi -automated system for Current-Voltage (I-V), Capacitance -Voltage (C-V), and Deep Level Transient Spectroscopy (DLTS) has been developed for the study of semiconductor devices. I -V, C-V, and DLTS measurements can be taken over a wide temperature range, from 100 K up to 450 K. Software for processing the data obtained has also been developed. This thesis presents the first reported successful measurements of deep levels in CuInSe_ 2 by DLTS measurements. The results indicate the presence in the p-type CuInSe_ 2 films of a majority-carrier (hole) trap located 0.70 eV above the valence band edge and a minority-carrier (electron) trap located 0.35 eV below the conduction band edge. Simulation studies show that the width and shape of the DLTS spectra for the hole trap can be explained only by assuming that the traps are distributed in energy around 0.70 eV. Our results are consistent with traps distributed from 0.65 to 0.75 eV, but it is not possible to determine uniquely the exact distribution. The electron trap at 0.35 eV does is not distributed in energy. There is strong evidence from the C-V, C-T, and I-V measurements, and indirectly from the DLTS measurements, that there is a large hole trap concentration in the CuInSe _ 2 layer close to the interface with the CdS. These interface states have a concentration of approximately 5 times 10 ^{15} cm^{ -3}, compared to a doping density in the CuInSe _ 2 layer of 1 times 10^{15} cm ^{-3}, a hole trap concentration of 5 times 10^{14 } cm^{-3}, and an electron trap concentration of 0.5 times 10^{14} cm ^{-3}. The I-V measurements are consistent with charge transport via an interface recombination/tunneling mechanism, where the tunneling is assisted by the interface states.

  18. Photoluminescence spectral study of single cadmium selenide/zinc sulfide colloidal nanocrystals in poly(methyl methacrylate) and quantum dots molecules

    NASA Astrophysics Data System (ADS)

    Shen, Yaoming

    Quantum dots (QDs)and Nano-crystals (NCs) have been studies for decades. Because of the nanoscale quantum confinement, delta shape like energy density states and narrowband emitters properties, they hold great promise for numerous optoelectronics and photonics applications. They could be used for tunable lasers, white LED, Nano-OLED, non-volatile memory and solar cells. They are also the most promising candidates for the quantum computing. The benefits for NCs over QDs is that NCs can be incorporated into a variety of polymers as well as thin films of bulk semiconductors. These exceptional flexibility and structural control distinguish NCs from the more traditional QD structures fabricated using epitaxial growth techniques. In my research of work, I studied the photoluminescence (PL) and absorption character of ensemble NCs incorporated in Polymethyl methacrylate (PMMA). To understand the behavior of the NCs in PMMA, it is important to measure a singe NC to avoid the inhomogenous broading of many NCs. So I particularly studied the behavior of a single NC in PMMA matrix. A microphotoluminescence setup to optically isolate a single nanocrystal is used. Random spectral shift and blinking behavior (on and off) are found. Addition to that, two color spectral shifting, is a major phenomena found in the system. Other interesting results such as PL intensity changes (decreasing or increasing with time) and quenching effect are observed and explained too. From the correlation function, we can distinguish the phonon replicas. The energy of these phonons can be calculated very accurately from the experiment result. The Huang-Rhys factors can be estimated too. Self-assembled semiconductor quantum dots (QDs), from highly strained-layer heteroepitaxy in the Stranski-Krastanow (S-K) growth mode, have been intensively studied because of the delta-function-like density of states, which is significant for optoelectronic applications. Spontaneous formation of semiconductor quantum

  19. Oxidation Studies of Copper-Indium and Stability Studies on Cadmium Copper-Indium Solar Cells.

    NASA Astrophysics Data System (ADS)

    Jamjoum, Osama Mohamed

    The subsequent aims of this thesis have been:. 1. To investigate the initial, thermal and anodic oxidation of p-type single-crystal CuInSe(,2) using complementary Auger electron spectroscopy (AES), secondary ion mass spectroscopy (SIMS) x-ray photoelectron spectroscopy (XPS), low energy loss spectroscopy (LELS) and ellipsometry. The air-grown and Br-Methanol etched CuInSe(,2) oxide is thin (20 - 40 (ANGSTROM)). Thermal oxides of CuInSe(,2) grow rapidly above 180(DEGREES)C. The oxides are predominately In(,2)O(,3) with less than 10% SeO(,2). No Cu or Cu-oxides were detected either by initial oxidation (LELS data) or thermal oxidation (XPS). The interface between the oxides was examined using AES depth-compositional profiling and XPS, and Cu(,x)Se is found to form at the interface during oxide growth. Oxide layer thicknesses and Se-3d electron escape depths were estimated from a consideration of XPS peak intensities. Unlike the thermal oxide, the anodic oxide was found to contain free Se and Cu-oxides (CuO and Cu(,2)O). However from this work it was not possible to confirm the formation of the Cu(,x)Se layer at the anodic oxide-semiconductor interface. 2. To investigate and correlate the compositional and chemical properties of the CdS/CuInSe(,2) solar cells with photovoltaic performance under various heat-treatments and prolonged illumination. These investigations show that: (1) The initial growth of CdS/CuInSe(,2) produces a mixed Cu(,2)S/Cu(,2)Se transition layer at the CdS/CuInSe(,2) interface. (2) The CdS/CuInSe(,2) is electrically and compositionally stable up to 170(DEGREES)C. However, at temperatures greater or equal to 240(DEGREES)C, diffusion of Cd into the Cu-ternary interface takes place. Such diffusion might be one of the reasons for cell degradation. (3) Cell performance has improved as a result of oxygen anneal. Two mechanisms have been suggested through this work that might account for such an improvement. (i) Formation of a thin layer of CdSO(,4

  20. One-step fabrication of copper sulfide nanoparticles decorated on graphene sheets as highly stable and efficient counter electrode for CdS-sensitized solar cells

    NASA Astrophysics Data System (ADS)

    Hessein, Amr; Wang, Feiju; Masai, Hirokazu; Matsuda, Kazunari; Abd El-Moneim, Ahmed

    2016-11-01

    Quantum-dot-sensitized solar cells (QDSSCs) are thin-film photovoltaics and highly promising as next-generation solar cells owing to their high theoretical efficiency, easy fabrication process, and low production cost. However, the practical photoconversion efficiencies (PCEs) of QDSSCs are still far below the theoretically estimated value owing to the lack of an applicable design of the materials and electrodes. In this work, we developed a highly stable and efficient counter electrode (CE) from copper sulfide nanocrystals and reduced graphene oxide (Cu x S@RGO) for QDSSC applications. The Cu x S@RGO electrocatalyst was successfully prepared by a facile one-pot hydrothermal method, then directly applied to a fluorine-doped tin oxide (FTO)-coated glass substrate by the simple drop-casting technique. Owing to the synergistic effect between Cu x S nanocrystals and conductive RGO sheets, the Cu x S@RGO CE showed high electrocatalytic activity for polysulfide electrolyte reduction. A CdS QDSSC based on the Cu x S@RGO CE yielded a high and reproducible PCE of 2.36%, exceeding those of 1.57 and 1.33% obtained with the commonly used Cu2S/brass and Pt CEs, respectively. Moreover, the QDSSC with the Cu x S@RGO CE showed excellent photostability in a light-soaking test without any obvious decay in the photocurrent, whereas the cell based on the Cu2S/brass CE was severely degraded.

  1. Spectral analysis of the effects of 1.7 MeV electron irradiation on the current transfer characteristic of cadmium telluride solar cells.

    PubMed

    Tian, Jin-Xiu; Zeng, Guang-Gen; He, Xu-Lin; Zhang, Jing-Quan; Wu, Li-Li; Li, Wei; Li, Bing; Wang, Wen-Wu; Feng, Liang-Huan

    2014-04-01

    The effects of device performance of 1.7 MeV electron irradiation on cadmium telluride polycrystalline thin film solar cells with the structure of anti-radiation glass/ITO/ZnO/CdS/CdTe/ZnTe/ZnTe : Cu/Ni have been studied. Light and dark I-V characteristics, dark C-V characteristics, quantum efficiency (QE), admittance spectrum (AS) and other testing methods were used to analyze cells performance such as the open-circuit voltage (Voc), short-circuit current (Isc), fill factor (FF) and conversion efficiency (eta). It was explored to find out the effects of irradiation on the current transfer characteristic of solar cells combined with the dark current density (Jo), diode ideal factor (A), quantum efficiency, carrier concentration and the depletion layer width. The decline in short-circuit current was very large and the efficiency of solar cells decreased obviously after irradiation. Reverse saturation current density increased, which indicates that p-n junction characteristics of solar cells were damaged, and diode ideal factor was almost the same, so current transport mechanism of solar cells has not changed. Quantum efficiency curves proved that the damage of solar cells' p-n junction influenced the collection of photo-generated carriers. Irradiation made carrier concentration reduce to 40.6%. The analyses have shown that. A new defect was induced by electron irradiation, whose position is close to 0.58 eV above the valence band in the forbidden band, and capture cross section is 1.78 x 10(-16) cm2. These results indicate that irradiation influences the generation of photo-generated carriers, increases the risk of the carrier recombination and the reverse dark current, and eventually makes the short-circuit current of solar cells decay.

  2. Errors in short circuit measurements due to spectral mismatch between sunlight and solar simulators

    NASA Technical Reports Server (NTRS)

    Curtis, H. B.

    1976-01-01

    Errors in short circuit current measurement were calculated for a variety of spectral mismatch conditions. The differences in spectral irradiance between terrestrial sunlight and three types of solar simulator were studied, as well as the differences in spectral response between three types of reference solar cells and various test cells. The simulators considered were a short arc xenon lamp AMO sunlight simulator, an ordinary quartz halogen lamp, and an ELH-type quartz halogen lamp. Three types of solar cells studied were a silicon cell, a cadmium sulfide cell and a gallium arsenide cell.

  3. Lead antimony sulfide (Pb5Sb8S17) solid-state quantum dot-sensitized solar cells with an efficiency of over 4%

    NASA Astrophysics Data System (ADS)

    Chang, Yi-Cheng; Suriyawong, Nipapon; Aragaw, Belete Asefa; Shi, Jen-Bin; Chen, Peter; Lee, Ming-Way

    2016-04-01

    Lead antimony sulfides are rare in nature and relatively unexplored ternary semiconductors. This work investigates the photovoltaic performance of Pb-Sb-S quantum dot-sensitized solar cells (QDSCs). Pb5Sb8S17 nanoparticles are grown on mesoporous TiO2 electrodes using the successive ionic layer adsorption reaction process. The synthesized Pb5Sb8S17 nanoparticles exhibit two attractive features for a good solar absorber material: a high optical absorption coefficient and a near optimal energy gap. Solid-state QDSCs are fabricated from the synthesized Pb5Sb8S17 nanoparticles using Spiro-OMeTAD as the hole-transporting material. The best cell yields a short-circuit current density Jsc of 11.92 mA cm-2, an open-circuit voltage Voc of 0.48 V, a fill factor FF of 30.7% and a power conversion efficiency (PCE) of 1.76% under 1sun. The external quantum efficiency (EQE) spectrum covers a spectral range of 350-800 nm with a maximal EQE = 65% at λ = 450 nm. At the reduced light intensity of 10% sun, the PCE increases to 4.14% with Jsc = 2.0 mA cm-2 (which could be normalized to 20 mA cm-2 under 1 sun). This PCE is 65% higher than the best previous result. The respectable PCE and Jsc indicate that Pb5Sb8S17 could be a potential candidate for a solar absorber material.

  4. Optimized approach to retrieve information on the tropospheric and stratospheric carbonyl sulfide (OCS) vertical distributions above Jungfraujoch from high-resolution FTIR solar spectra.

    NASA Astrophysics Data System (ADS)

    Lejeune, Bernard; Mahieu, Emmanuel; Servais, Christian; Duchatelet, Pierre; Demoulin, Philippe

    2010-05-01

    Carbonyl sulfide (OCS), which is produced in the troposphere from both biogenic and anthropogenic sources, is the most abundant gaseous sulfur species in the unpolluted atmosphere. Due to its low chemical reactivity and water solubility, a significant fraction of OCS is able to reach the stratosphere where it is converted to SO2 and ultimately to H2SO4 aerosols (Junge layer). These aerosols have the potential to amplify stratospheric ozone destruction on a global scale and may influence Earth's radiation budget and climate through increasing solar scattering. The transport of OCS from troposphere to stratosphere is thought to be the primary mechanism by which the Junge layer is sustained during nonvolcanic periods. Because of this, long-term trends in atmospheric OCS concentration, not only in the troposphere but also in the stratosphere, are of great interest. A new approach has been developed and optimized to retrieve atmospheric abundance of OCS from high-resolution ground-based infrared solar spectra by using the SFIT-2 (v3.91) algorithm, including a new model for solar lines simulation (solar lines often produce significant interferences in the OCS microwindows). The strongest lines of the ν3 fundamental band of OCS at 2062 cm-1 have been systematically evaluated with objective criteria to select a new set of microwindows, assuming the HITRAN 2004 spectroscopic parameters with an increase in the OCS line intensities of the ν3band main isotopologue 16O12C32S by 15.79% as compared to HITRAN 2000 (Rothman et al., 2008, and references therein). Two regularization schemes have further been compared (deducted from ATMOS and ACE-FTS measurements or based on a Tikhonov approach), in order to select the one which optimizes the information content while minimizing the error budget. The selected approach has allowed us to determine updated OCS long-term trend from 1988 to 2009 in both the troposphere and the stratosphere, using spectra recorded on a regular basis with

  5. Carbonyl sulfide

    Integrated Risk Information System (IRIS)

    Carbonyl sulfide ; CASRN 463 - 58 - 1 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Noncarcinogenic

  6. Hydrogen sulfide

    Integrated Risk Information System (IRIS)

    Hydrogen sulfide ; 7783 - 06 - 4 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Noncarcinogenic Effec

  7. Selenium sulfide

    Integrated Risk Information System (IRIS)

    Selenium sulfide ; CASRN 7446 - 34 - 6 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for Noncarcinogenic

  8. Cadmium zinc sulfide by solution growth

    SciTech Connect

    Chen, W.S.

    1992-05-12

    This patent describes a photoelectric cell. It comprises a thin film of CdZnS that forms a continuous coating free of pin holes and has a thickness that is sufficiently thin to provide at least 70% transmission of radiation having a wavelength 400 nm.

  9. Sulfidation of Cadmium at the Nanoscale

    SciTech Connect

    Cabot, Andreu; Smith, Rachel; Yin, Yadong; Zheng, Haimei; Reinhard, Bjorn; Liu, Haitao; Alivisatos, A. Paul

    2008-05-22

    We investigate the evolution of structures that result when spherical Cd nanoparticles of a few hundred nanometers in diameter react with dissolved molecular sulfur species in solution to form hollow CdS. Over a wide range of temperatures and concentrations, we find that rapid Cd diffusion through the growing CdS shell localizes the reaction front at the outermost CdS/S interface, leading to hollow particles when all the Cd is consumed. When we examine partially reacted particles, we find that this system differs significantly from others in which the nanoscale Kirkendall effect has been used to create hollow particles. In previously reported systems, partial reaction creates a hollow particle with a spherically symmetric metal core connected to the outer shell by filaments. In contrast, here we obtain a lower symmetry structure, in which the unreacted metal core and the coalesced vacancies separate into two distinct spherical caps, minimizing the metal/void interface. This pattern of void coalescence is likely to occur in situations where the metal/vacancy self-diffusivities in the core are greater than the diffusivity of the cations through the shell.

  10. Investigation of photoresponse in cadmium sulfide nanoparticles

    SciTech Connect

    Mishra, Sheo K. E-mail: dr.sheokmishra@gmail.com; Tripathi, Akhilesh; Shukla, R. K.; Srivastava, Rajneesh K.; Dubey, K. C.

    2015-06-24

    In this work, we report on the photo-response of CdS nanoparticles prepared by simple solid state reaction method. The X-ray diffraction (XRD) study has confirmed the formation of cubical zinc blende (c) phase. In the photo-response study, voltage dependence of photocurrent and darkcurrent as well as temporal rise and decay of photocurrent of CdS nanoparticles have been investigated. The photo-response of prepared sample has been measured under visible illumination using thick film of powder with out any binder. The photocurrent (I{sub pc}) and darkcurrent (I{sub dc}) follow power law with applied voltage i.e. I α V{sup r}. The rise and decay of photocurrent show negative photoconductivity.

  11. Mineral of the month: cadmium

    USGS Publications Warehouse

    Klimasauskas, Edward

    2005-01-01

    Cadmium, which was once used almost exclusively for pigments, now has many diverse applications. Cadmium’s low melting point, excellent electrical conductivity and resistance to corrosion make it valuable for many products including batteries, electroplated coatings, stabilizers for plastics, solar cells and nonferrous alloys. Today’s cadmium is primarily used in rechargeable batteries, accounting for about 78 percent of consumption in 2004. In 2000, an estimated 3.5 billion consumer batteries were sold in the United States, of which almost 10 percent were nickel-cadmium batteries.

  12. Wurtzite copper-zinc-tin sulfide as a superior counter electrode material for dye-sensitized solar cells

    PubMed Central

    2013-01-01

    Wurtzite and kesterite Cu2ZnSnS4 (CZTS) nanocrystals were employed as counter electrode (CE) materials for dye-sensitized solar cells (DSSCs). Compared to kesterite CZTS, the wurtzite CZTS exhibited higher electrocatalytic activity for catalyzing reduction of iodide electrolyte and better conductivity. Accordingly, the DSSC with wurtzite CZTS CE generated higher power conversion efficiency (6.89%) than that of Pt (6.23%) and kesterite CZTS (4.89%) CEs. PMID:24191954

  13. Wurtzite copper-zinc-tin sulfide as a superior counter electrode material for dye-sensitized solar cells

    NASA Astrophysics Data System (ADS)

    Kong, Jun; Zhou, Zheng-Ji; Li, Mei; Zhou, Wen-Hui; Yuan, Sheng-Jie; Yao, Rong-Yue; Zhao, Yang; Wu, Si-Xin

    2013-11-01

    Wurtzite and kesterite Cu2ZnSnS4 (CZTS) nanocrystals were employed as counter electrode (CE) materials for dye-sensitized solar cells (DSSCs). Compared to kesterite CZTS, the wurtzite CZTS exhibited higher electrocatalytic activity for catalyzing reduction of iodide electrolyte and better conductivity. Accordingly, the DSSC with wurtzite CZTS CE generated higher power conversion efficiency (6.89%) than that of Pt (6.23%) and kesterite CZTS (4.89%) CEs.

  14. Inorganic phosphate accumulation and cadmium detoxification in Klebsiella aerogenes NCTC 418 growing in continuous culture

    SciTech Connect

    Aiking, H.; Stijnman, A.; van Garderen, C.; van Heerikhuizen, H.; van Riet, J.

    1984-02-01

    Klebsiella aerogenes NCTC-418, growing in the presence of cadmium under glucose-, sulfate-, or phosphate-limited conditions in continuous culture, exhibits two different cadmium detoxifying mechanisms. In addition to sulfide formation, increased accumulation of P/sub i/ is demonstrated as a novel mechanism. Intracellular cadmium is always quantitatively counterbalanced by a concerted increase in both inorganic sulfide and P/sub i/ contents of the cells. This led to the conclusion that production of sulfide and accumulation of P/sub i/ are detoxification mechanisms present in K. aerogenes but that their relative importance is crucially dependent on the strain and the growth conditions employed.

  15. Methods for improving solar cell open circuit voltage

    DOEpatents

    Jordan, John F.; Singh, Vijay P.

    1979-01-01

    A method for producing a solar cell having an increased open circuit voltage. A layer of cadmium sulfide (CdS) produced by a chemical spray technique and having residual chlorides is exposed to a flow of hydrogen sulfide (H.sub.2 S) heated to a temperature of 400.degree.-600.degree. C. The residual chlorides are reduced and any remaining CdCl.sub.2 is converted to CdS. A heterojunction is formed over the CdS and electrodes are formed. Application of chromium as the positive electrode results in a further increase in the open circuit voltage available from the H.sub.2 S-treated solar cell.

  16. Thin film cadmium telluride, zinc telluride, and mercury zinc telluride solar cells. Final subcontract report, 1 July 1988--31 December 1991

    SciTech Connect

    Chu, T.L.

    1992-04-01

    This report describes research to demonstrate (1) thin film cadmium telluride solar cells with a quantum efficiency of 75% or higher at 0. 44 {mu}m and a photovoltaic efficiency of 11.5% or greater, and (2) thin film zinc telluride and mercury zinc telluride solar cells with a transparency to sub-band-gap radiation of 65% and a photovoltaic conversion efficiency of 5% and 8%, respectively. Work was directed at (1) depositing transparent conducting semiconductor films by solution growth and metal-organic chemical vapor deposition (MOCVD) technique, (2) depositing CdTe films by close-spaced sublimation (CSS) and MOCVD techniques, (3) preparing and evaluating thin film CdTe solar cells, and (4) preparing and characterizing thin film ZnTe, CD{sub 1-x}Zn{sub 1-x}Te, and Hg{sub 1-x}Zn{sub x}Te solar cells. The deposition of CdS films from aqueous solutions was investigated in detail, and their crystallographic, optical, and electrical properties were characterized. CdTe films were deposited from DMCd and DIPTe at 400{degrees}C using TEGa and AsH{sub 3} as dopants. CdTe films deposited by CSS had significantly better microstructures than those deposited by MOCVD. Deep energy states in CdTe films deposited by CSS and MOCVD were investigated. Thin films of ZnTe, Cd{sub 1- x}Zn{sub x}Te, and Hg{sub 1-x}Zn{sub x}Te were deposited by MOCVD, and their crystallographic, optical, and electrical properties were characterized. 67 refs.

  17. Nanocomposite of tin sulfide nanoparticles with reduced graphene oxide in high-efficiency dye-sensitized solar cells.

    PubMed

    Yang, Bo; Zuo, Xueqin; Chen, Peng; Zhou, Lei; Yang, Xiao; Zhang, Haijun; Li, Guang; Wu, Mingzai; Ma, Yongqing; Jin, Shaowei; Chen, Xiaoshuang

    2015-01-14

    A nanocomposite of SnS2 nanoparticles with reduced graphene oxide (SnS2@RGO) had been successfully synthesized as a substitute conventional Pt counter electrode (CE) in a dye-sensitized solar cell (DSSC) system. The SnS2 nanoparticles were uniformly dispersed onto graphene sheets, which formed a nanosized composite system. The effectiveness of this nanocomposite exhibited remarkable electrocatalytic properties upon reducing the triiodide, owning to synergistic effects of SnS2 nanoparticles dispersed on graphene sheet and improved conductivity. Consequently, the DSSC equipped with SnS2@RGO nanocomposite CE achieved power conversion efficiency (PCE) of 7.12%, which was higher than those of SnS2 nanoparticles (5.58%) or graphene sheet alone (3.73%) as CEs and also comparable to the value (6.79%) obtained with pure Pt CE as a reference.

  18. Synthesis of Bi2S3 quantum dots for sensitized solar cells by reverse SILAR

    NASA Astrophysics Data System (ADS)

    Singh, Navjot; Sharma, J.; Tripathi, S. K.

    2016-05-01

    Quantum Dot Sensitized Solar cells (QDSSC) have great potential to replace silicon-based solar cells. Quantum dots of various materials and sizes could be used to convert most of the visible light into the electrical current. This paper put emphasis on the synthesis of Bismuth Sulphide quantum dots and selectivity of the anionic precursor by Successive Ionic Layer Adsorption Reaction (SILAR). Bismuth Sulfide (Bi2S3) (group V - Vi semiconductor) is strong contestant for cadmium free solar cells due to its optimum band gap for light harvesting. Optical, structural and electrical measurements are reported and discussed. Problem regarding the choice of precursor for anion extraction is discussed. Band gap of the synthesized quantum dots is 1.2 eV which does not match with the required energy band gap of bismuth sulfide that is 1.7eV.

  19. The Determination of Hydrogen Sulfide in Stack Gases, Iodometric Titration After Sulfite Removal.

    ERIC Educational Resources Information Center

    Robles, E. G.

    The determination of hydrogen sulfide in effluents from coal-fired furnaces and incinerators is complicated by the presence of sulfur oxides (which form acids). Organic compounds also may interfere with or prevent the formation of the cadmium sulfide precipitate or give false positive results because of reaction with iodine. The report presents a…

  20. In-situ growth of antimony sulfide in carbon nanoparticle matrix: Enhanced electrocatalytic activity as counter electrode in dye-sensitized solar cells

    NASA Astrophysics Data System (ADS)

    Sun, Panpan; Zhang, Ming; Ai, Changzhi; Wu, Zhixin; Lu, Shuang; Zhang, Xintong; Huang, Niu; Sun, Yihua; Sun, Xiaohua

    2016-07-01

    Considering the undesirable electrocatalytic activity toward I-/I3- redox system of prinstine antimony sulfide (Sb2S3) fabricated with the existing conditions, a mesoporous carbon nanoparticle film (CNP) is introduced here for in-situ growth of Sb2S3 to construct a Sb2S3@CNP hybrid catalyst. Based on a Sb-thiourea precursor solution, in-situ growth of Sb2S3 can be achieved via solution deposition (denoted as Sb2S3@CNP-S) as well as atmospheric pressure thermal evaporation (denoted as Sb2S3@CNP-T) in CNP matrix. Structural characterizations indicate that Sb2S3 particles have well dispersed in the pores of CNP matrix. Because of the introduction of porous and conductive CNP matrix to support Sb2S3, the hybrid catalyst exhibits lower charge transfer resistance at the catalyst/electrolyte interface and higher electrocatalytic activity. When used as counter electrode (CE) for dye-sensitized solar cells (DSSCs), devices using Sb2S3@CNP hybrid catalyst as CE produce fill factor of 67.6% and 66.3%, which is significantly higher than that using pristine Sb2S3 fabricated in our previous work (52.8%). Finally, the corresponding power conversion efficiencies reach 6.69% (Sb2S3@CNP-S) and 6.24% (Sb2S3@CNP-T), respectively, which are comparable to that using Pt CE measured under the same conditions (6.74%).

  1. Labile sulfide and sulfite in phytochelatin complexes

    SciTech Connect

    Eannetta, N.T.; Steffens, J.C. )

    1989-04-01

    Heavy metals such as cadmium induce tomato cell cultures to synthesize the metal binding polypeptides ({gamma}-Glu-Cys){sub 3} and ({gamma}-Glu-Cys){sub 4}-Gly (phytochelatins). Tomato cells selected for growth on normally lethal concentrations of CdCl{sub 2} synthesize higher quantities of these polypeptides. Cd{sup r} cells are not cross-resistant to other heavy metals, and recent work suggests that metal detoxification by these peptides may be Cd-specific. The occurrence of labile sulfur as a component of the metal complex raises questions concerning possible functions of phytochelatins besides that of Cd binding. The presence of acid-labile sulfide ion in phytochelatin complexes has been reported by several groups. We report the additional finding that labile sulfite is also present in these complexes and in higher amounts than sulfide. Sulfide and sulfite are both released from the metal binding complex by acidification or by treatment with EDTA.

  2. Sulfide chemiluminescence detection

    DOEpatents

    Spurlin, Stanford R.; Yeung, Edward S.

    1985-01-01

    A method of chemiluminescently determining a sulfide which is either hydrogen sulfide or methyl mercaptan by reacting the sulfide with chlorine dioxide at low pressure and under conditions which allow a longer reaction time in emission of a single photon for every two sulfide containing species, and thereafter, chemiluminescently detecting and determining the sulfide. The invention also relates not only to the detection method, but the novel chemical reaction and a specifically designed chemiluminescence detection cell for the reaction.

  3. Sulfide chemiluminescence detection

    DOEpatents

    Spurlin, S.R.; Yeung, E.S.

    1985-11-26

    A method is described for chemiluminescently determining a sulfide which is either hydrogen sulfide or methyl mercaptan by reacting the sulfide with chlorine dioxide at low pressure and under conditions which allow a longer reaction time in emission of a single photon for every two sulfide containing species, and thereafter, chemiluminescently detecting and determining the sulfide. The invention also relates not only to the detection method, but the novel chemical reaction and a specifically designed chemiluminescence detection cell for the reaction. 4 figs.

  4. BIOLOGICAL RESPONSE TO VARIATION OF ACID-VOLATILE SULFIDES AND METALS IN FIELD-EXPOSED SPIKED SEDIMENTS

    EPA Science Inventory

    Vertical and temporal variations of acid-volatile sulfides (AVS) and simultaneously extracted metals (SEM) in sediment can control biological impacts of metals. To assess the significance of these variations in field sediments, sediments spiked with cadmium, copper, lead, nickel ...

  5. Metabolic Engineering of an Aerobic Sulfate Reduction Pathway and Its Application to Precipitation of Cadmium on the Cell Surface

    PubMed Central

    Wang, Clifford L.; Maratukulam, Priya D.; Lum, Amy M.; Clark, Douglas S.; Keasling, J. D.

    2000-01-01

    The conversion of sulfate to an excess of free sulfide requires stringent reductive conditions. Dissimilatory sulfate reduction is used in nature by sulfate-reducing bacteria for respiration and results in the conversion of sulfate to sulfide. However, this dissimilatory sulfate reduction pathway is inhibited by oxygen and is thus limited to anaerobic environments. As an alternative, we have metabolically engineered a novel aerobic sulfate reduction pathway for the secretion of sulfides. The assimilatory sulfate reduction pathway was redirected to overproduce cysteine, and excess cysteine was converted to sulfide by cysteine desulfhydrase. As a potential application for this pathway, a bacterium was engineered with this pathway and was used to aerobically precipitate cadmium as cadmium sulfide, which was deposited on the cell surface. To maximize sulfide production and cadmium precipitation, the production of cysteine desulfhydrase was modulated to achieve an optimal balance between the production and degradation of cysteine. PMID:11010904

  6. Cadmium-free junction fabrication process for CuInSe{sub 2} thin film solar cells

    SciTech Connect

    Ramanathan, K.V.; Contreras, M.A.; Bhattacharya, R.N.; Keane, J.; Noufi, R.

    1999-09-07

    The present invention provides an economical, simple, dry and controllable semiconductor layer junction forming process to make cadmium free high efficiency photovoltaic cells having a first layer comprised primarily of copper indium diselenide having a thin doped copper indium diselenide n-type region, generated by thermal diffusion with a group II(b) element such as zinc, and a halide, such as chlorine, and a second layer comprised of a conventional zinc oxide bilayer. A photovoltaic device according the present invention includes a first thin film layer of semiconductor material formed primarily from copper indium diselenide. Doping of the copper indium diselenide with zinc chloride is accomplished using either a zinc chloride solution or a solid zinc chloride material. Thermal diffusion of zinc chloride into the copper indium diselenide upper region creates the thin n-type copper indium diselenide surface. A second thin film layer of semiconductor material comprising zinc oxide is then applied in two layers. The first layer comprises a thin layer of high resistivity zinc oxide. The second relatively thick layer of zinc oxide is doped to exhibit low resistivity.

  7. Cadmium-free junction fabrication process for CuInSe.sub.2 thin film solar cells

    DOEpatents

    Ramanathan, Kannan V.; Contreras, Miguel A.; Bhattacharya, Raghu N.; Keane, James; Noufi, Rommel

    1999-01-01

    The present invention provides an economical, simple, dry and controllable semiconductor layer junction forming process to make cadmium free high efficiency photovoltaic cells having a first layer comprised primarily of copper indium diselenide having a thin doped copper indium diselenide n-type region, generated by thermal diffusion with a group II(b) element such as zinc, and a halide, such as chlorine, and a second layer comprised of a conventional zinc oxide bilayer. A photovoltaic device according the present invention includes a first thin film layer of semiconductor material formed primarily from copper indium diselenide. Doping of the copper indium diselenide with zinc chloride is accomplished using either a zinc chloride solution or a solid zinc chloride material. Thermal diffusion of zinc chloride into the copper indium diselenide upper region creates the thin n-type copper indium diselenide surface. A second thin film layer of semiconductor material comprising zinc oxide is then applied in two layers. The first layer comprises a thin layer of high resistivity zinc oxide. The second relatively thick layer of zinc oxide is doped to exhibit low resistivity.

  8. I-III-VI.sub.2 based solar cell utilizing the structure CuInGaSe.sub.2 CdZnS/ZnO

    DOEpatents

    Chen, Wen S.; Stewart, John M.

    1992-01-07

    A thin film I-III-VI.sub.2 based solar cell having a first layer of copper indium gallium selenide, a second layer of cadmium zinc sulfide, a double layer of zinc oxide, and a metallization structure comprised of a layer of nickel covered by a layer of aluminum. An optional antireflective coating may be placed on said metallization structure. The cadmium zinc sulfide layer is deposited by means of an aqueous solution growth deposition process and may actually consist of two layers: a low zinc content layer and a high zinc content layer. Photovoltaic efficiencies of 12.5% at Air Mass 1.5 illumination conditions and 10.4% under AMO illumination can be achieved.

  9. Effect of chlorine activation treatment on electron beam induced current signal distribution of cadmium telluride thin film solar cells

    NASA Astrophysics Data System (ADS)

    Zywitzki, Olaf; Modes, Thomas; Morgner, Henry; Metzner, Christoph; Siepchen, Bastian; Späth, Bettina; Drost, Christian; Krishnakumar, Velappan; Frauenstein, Sven

    2013-10-01

    We have investigated CdTe thin film solar cells without activation treatment and with CdCl2 activation treatment at temperatures between 370 and 430 °C using a constant activation time of 25 min. For this purpose, CdS/CdTe layers were deposited by closed-space-sublimation on FTO coated float glass. The solar cells were characterized by measurements of the JV characteristics and quantum efficiencies. In addition, ion polished cross sections of the solar cells were prepared for high-resolution FE-SEM imaging of the microstructure and the simultaneous registration of electron beam induced current (EBIC) signal distribution. By measurement of the EBIC signal distribution, it can be shown that without activation treatment the CdTe grain boundaries itself and grain boundary near regions exhibit no EBIC signal, whereas centres of some singular grains already show a distinct EBIC signal. In contrast, after the chlorine activation treatment, the grain boundary near regions exhibit a significant higher EBIC signal than the centre of the grains. The results can be discussed as a direct evidence for defect passivation of grain boundary near regions by the chlorine activation treatment. At activation temperature of 430 °C, additionally, a significant grain growth and agglomeration of the CdS layer can be recognized, which is linked with the formation of voids within the CdS layer and a deterioration of pn junction properties.

  10. SULFIDE MINERALS IN SEDIMENTS

    EPA Science Inventory

    The formation processes of metal sulfides in sediments, especially iron sulfides, have been the subjects of intense scientific research because of linkages to the global biogeochemical cycles of iron, sulfur, carbon, and oxygen. Transition metal sulfides (e.g., NiS, CuS, ZnS, Cd...

  11. Iron monosulfide as a scavenger for dissolved hexavalent chromium and cadmium.

    PubMed

    Jo, S; Lee, J Y; Kong, S H; Choi, J; Park, J W

    2008-09-01

    Iron sulfide minerals are common components of soil/sedimentary environments. Reactions near the surfaces of iron sulfides play important roles in metal retention, mobility, and bioavailability. A series of batch experiments was conducted to study the removal of aqueous chromium and cadmium by iron monosulfide. Hexavalent chromium was reduced to Cr(III) by iron monosulfide with simultaneous precipitation of chromium and iron oxyhydroxide. In contrast to chromium, the primary retention mechanism of cadmium by iron monosulfide was lattice exchange. Surface adsorption to iron monosulfide and precipitation with sulfide on the iron monosulfide surface also contributed to the removal of aqueous cadmium. New phases of both chromium and cadmium were confirmed with transmission electron microscopy. The solution pH was an important factor in this research; it can change particle surface charge and metal species, hence affecting the removal of chromium, but not cadmium. Ferrous ions without FeS exhibited less Cr(VI) removal than with FeS, which might be owing to sulfides from FeS and the existence of the solid phase. Iron monosulfide exhibited higher removal efficiency for chromium and cadmium than zero valent iron and other iron oxide minerals, and the synergistic effect of ferrous iron and sulfide appeared to cause this result.

  12. The Search for Interstellar Sulfide Grains

    NASA Technical Reports Server (NTRS)

    Keller, Lindsay P.; Messenger, Scott

    2010-01-01

    The lifecycle of sulfur in the galaxy is poorly understood. Fe-sulfide grains are abundant in early solar system materials (e.g. meteorites and comets) and S is highly depleted from the gas phase in cold, dense molecular cloud environments. In stark contrast, sulfur is essentially undepleted from the gas phase in the diffuse interstellar medium, indicating that little sulfur is incorporated into solid grains in this environment. It is widely believed that sulfur is not a component of interstellar dust grains. This is a rather puzzling observation unless Fe-sulfides are not produced in significant quantities in stellar outflows, or their lifetime in the ISM is very short due to rapid destruction. Fe sulfide grains are ubiquitous in cometary samples where they are the dominant host of sulfur. The Fe-sulfides (primarily pyrrhotite; Fe(1-x)S) are common, both as discrete 0.5-10 micron-sized grains and as fine (5-10 nm) nanophase inclusions within amorphous silicate grains. Cometary dust particles contain high abundances of well-preserved presolar silicates and organic matter and we have suggested that they should contain presolar sulfides as well. This hypothesis is supported by the observation of abundant Fe-sulfides grains in dust around pre- and post-main sequence stars inferred from astronomical spectra showing a broad 23 micron IR feature due to FeS. Fe-sulfide grains also occur as inclusions in bona fide circumstellar amorphous silicate grains and as inclusions within deuterium-rich organic matter in cometary dust samples. Our irradiation experiments show that FeS is far more resistant to radiation damage than silicates. Consequently, we expect that Fe sulfide stardust should be as abundant as silicate stardust in solar system materials.

  13. Polycrystalline thin film cadmium telluride solar cells fabricated by electrodeposition. Annual technical report, 20 March 1995--19 March 1996

    SciTech Connect

    Trefny, J U; Mao, D

    1997-04-01

    The objective of this project is to develop improved processes for fabricating CdTe/CdS polycrystalline thin-film solar cells. Researchers used electrodeposition to form CdTe; electrodeposition is a non-vacuum, low-cost technique that is attractive for economic, large-scale production. During the past year, research and development efforts focused on several steps that are most critical to the fabricating high-efficiency CdTe solar cells. These include the optimization of the CdTe electrodeposition process, the effect of pretreatment of CdS substrates, the post-deposition annealing of CdTe, and back-contact formation using Cu-doped ZnTe. Systematic investigations of these processing steps have led to a better understanding and improved performance of the CdTe-based cells. Researchers studied the structural properties of chemical-bath-deposited CdS thin films and their growth mechanisms by investigating CdS samples prepared at different deposition times; investigated the effect of CdCl{sub 2} treatment of CdS films on the photovoltaic performance of CdTe solar cells; studied Cu-doped ZnTe as a promising material for forming stable, low-resistance contacts to the p-type CdTe; and investigated the effect of CdTe and CdS thickness on the photovoltaic performance of the resulting cells. As a result of their systematic investigation and optimization of the processing conditions, researchers improved the efficiency of CdTe/CdS cells using ZnTe back-contact and electrodeposited CdTe. The best CdTe/CdS cell exhibited a V{sub oc} of 0.778 V, a J{sub sc} of 22.4 mA/cm{sup 2}, a FF of 74%, and an efficiency of 12.9% (verified at NREL). In terms of individual parameters, researchers obtained a V{sub oc} over 0.8 V and a FF of 76% on other cells.

  14. Surface passivation of lead sulfide nanocrystals with low electron affinity metals: photoluminescence and photovoltaic performance.

    PubMed

    Tavakoli, Mohammad Mahdi; Mirfasih, Mohammad Hassan; Hasanzadeh, Soheil; Aashuri, Hossein; Simchi, Abdolreza

    2016-04-28

    During the last decade, solution-processed colloidal quantum dots (CQDs) have attracted significant attention for low-cost fabrication of optoelectronic devices. In this study, lead sulfide (PbS) CQDs were synthesized via the hot injection method and the effect of doping elements with low electron affinity, including cadmium, calcium and zinc, on the passivation of trap states was investigated. A red-shift in the luminescence emission was observed by doping through passivation of lead dangling bonds. Time-resolved photoluminescence measurements showed that the lifetime of charged carriers was significantly enhanced by cadmium doping (∼80%) which is quite noticeable compared with calcium- and zinc-doped nanocrystals. External quantum efficiency measurements on thin solid films (∼300 nm) prepared by spin coating supported improved lifetime of carriers through passivation of mid-gap trap states. In order to show the potential application of the doping process, bulk heterojunction CQD solar cells were fabricated. It was found that the power conversion efficiency (PCE) was improved up to ∼40%; the highest improvement was observed with the Cd treatment. Finally, density functional theory (DFT) and electrochemical impedance spectroscopy (EIS) were employed to study the effect of doping on the density of states. The results showed that doping with low electron affinity metals effectively reduced the deep trap states of PbS QDs.

  15. CdS and CdS/CdSe sensitized ZnO nanorod array solar cells prepared by a solution ions exchange process

    SciTech Connect

    Chen, Ling; Gong, Haibo; Zheng, Xiaopeng; Zhu, Min; Zhang, Jun; Yang, Shikuan; Cao, Bingqiang

    2013-10-15

    Graphical abstract: - Highlights: • CdS and CdS/CdSe quantum dots are assembled on ZnO nanorods by ion exchange process. • The CdS/CdSe sensitization of ZnO effectively extends the absorption spectrum. • The performance of ZnO/CdS/CdSe cell is improved by extending absorption spectrum. - Abstract: In this paper, cadmium sulfide (CdS) and cadmium sulfide/cadmium selenide (CdS/CdSe) quantum dots (QDs) are assembled onto ZnO nanorod arrays by a solution ion exchange process for QD-sensitized solar cell application. The morphology, composition and absorption properties of different photoanodes were characterized with scanning electron microscope, transmission electron microscope, energy-dispersive X-ray spectrum and Raman spectrum in detail. It is shown that conformal and uniform CdS and CdS/CdSe shells can grow on ZnO nanorod cores. Quantum dot sensitized solar cells based on ZnO/CdS and ZnO/CdS/CdSe nanocable arrays were assembled with gold counter electrode and polysulfide electrolyte solution. The CdS/CdSe sensitization of ZnO can effectively extend the absorption spectrum up to 650 nm, which has a remarkable impact on the performance of a photovoltaic device by extending the absorption spectrum. Preliminary results show one fourth improvement in solar cell efficiency.

  16. Alternative quaternary chalcopyrite sulfides (Cu2FeSnS4 and Cu2CoSnS4) as electrocatalyst materials for counter electrodes in dye-sensitized solar cells

    NASA Astrophysics Data System (ADS)

    Mokurala, Krishnaiah; Mallick, Sudhanshu; Bhargava, Parag

    2016-02-01

    Quaternary chalcopyrite sulfides are attracting considerable interest as electrocatalysts for triiodide reduction in dye-sensitized solar cells (DSSCs). Conventionally, the much expensive platinum (Pt) is being used as an electrocatalyst material for counter electrodes (CEs) in DSSCs. The present study reports the synthesis of quaternary chalcopyrite sulfides (Cu2FeSnS4 (CFTS) and Cu2CoSnS4 (CCTS) nanoparticles for their application as alternative CE materials in DSSCs. For the first time, CCTS is being explored as a CE material for DSSCs. Physical properties such as crystal structure, elemental composition and morphological characteristics of the as synthesized nanoparticles and the sulfurized films are studied. Cyclic voltammetry, electrochemical impedance spectroscopy (EIS) and Tafel polarization measurements demonstrated that the CCTS CE is more effective for tri-iodide reduction as compared to CFTS CE. The photo conversion efficiencies (PCEs) of DSSCs fabricated using CCTS and CFTS as CEs are found to be 7.4% and 7.1% respectively, while DSSC fabricated with Pt as the CE showed an efficiency of 8.2%. This indicates that they both can potentially be used as alternative CE materials in DSSCs in place of the more expensive Pt.

  17. Experimental and theoretical investigations of cadmium diffusion in vacancy-rich Cu(In, Ga)Se2 material

    NASA Astrophysics Data System (ADS)

    Biderman, Norbert J.

    Copper indium gallium selenide (Cu(In,Ga)Se2 or CIGS) has become a significant topic of research and development for photovoltaic application. CIGS photovoltaic devices have demonstrated record conversion efficiencies however are still below the maximum solar conversion efficiency. Losses in performance have been attributed structural defects including vacancies, doping, grain boundaries, and compositional non-uniformity that are poorly understood and controlled. The cadmium sulfide (CdS) buffer layer plays a critical role in high-performance CIGS photovoltaic devices, serving as the n-type component of the p-n junction formed with the p-type CIGS absorber layer. Cadmium diffusion into the CIGS surface during CdS deposition creates a buried p-n homojunction in addition to the CIGS/CdS p-n heterojunction. CdS is believed to assist in reducing carrier recombination at the CIGS/CdS interface, an important attribute of high-efficiency solar cells. In the present work, cadmium diffusion mechanisms in CIGS are experimentally investigated via secondary ion mass spectroscopy (SIMS) and Auger electron spectroscopy (AES). Two cadmium diffusion profiles with distinct Arrhenius diffusion kinetics within a single depth profile of the CIGS thin film are observed with SIMS and AES: an intense first-stage diffusion profile directly below the CIGS/CdS interface and a long-range, second-stage diffusion profile that extends deep into the thin film. Cadmium grain boundary diffusion is also detected in fine-grain CIGS samples. These multiple diffusion processes are quantified in the present work, and the two-stage cadmium diffusion profiles suggest distinctive lattice diffusion mechanisms. Calculations and modeling of general impurity diffusion via interstitial sites in CIGS are also conducted via numerical including cadmium, iron, and zinc. In the numerical simulations, the standard diffusion-reaction kinetics theory is extended to vacancy-rich materials like CIGS that contain 1 at

  18. Direct examination of cadmium bonding in rat tissues dosed with mine wastes and cadmium-containing solutions

    SciTech Connect

    Diacomanolis, V.; Ng, J. C.; Sadler, R.; Harris, H. H.; Nomura, M.; Noller, B. N.

    2010-06-23

    Direct examination by XANES and EXAFS of metal bonding in tissue can be demonstrated by examining cadmium uptake and bonding in animal tissue maintained at cryogenic temperatures. XANES at the K-edge of cadmium were collected at the Photon Factory Advanced Ring (PF-AR), NW10A beam line at KEK-Tsukuba-Japan. Rats fed with 1g mine waste containing 8-400 mg/kg cadmium per 200g body weight (b.w.) or dosed by oral gavage with either cadmium chloride solution alone (at 6 mg/kg b.w.) or in combination with other salts (As, Cu or Zn), 5 days/week for 6 weeks, had 0.1-7.5 and 8-86 mg/kg cadmium in the liver or kidney, respectively. Rats given intraperitoneally (ip) or intravenously (iv) 1-4 times with 1 mg/kg b.w. cadmium solution had 30-120 mg/kg cadmium in the liver or kidney. Tissues from rats were kept and transferred at cryogenic temperature and XANES were recorded at 20 K. The spectra for rat liver samples suggested conjugation of cadmium with glutathione or association with the sulfide bond (Cd-S) of proteins and peptides. EXAFS of rat liver fed by Cd and Zn solutions showed that Cd was clearly bound to S ligands with an inter-atomic distance of 2.54 A ring for Cd-S that was similar to cadmium sulfide with an inter-atomic distance of 2.52 A ring for Cd-S. Liver or kidney of rats fed with mine wastes did not give an edge in the XANES spectra indicating little uptake of cadmium by the animals. Longer and higher dosing regimen may be required in order to observe the same Cd-S bond in the rat tissue from mine wastes, including confirmation by EXAFS.

  19. Low cost preparation of Cu2ZnSnS4 and Cu2ZnSn(SxSe1-x)4 from binary sulfide nanoparticles for solar cell application

    NASA Astrophysics Data System (ADS)

    Chen, Guilin; Yuan, Chenchen; Liu, Jiwan; Deng, Yitao; Jiang, Guoshun; Liu, Weifeng; Zhu, Changfei

    2014-09-01

    A low-cost non-vacuum process for fabrication of Cu2ZnSnS4 (CZTS) and Cu2ZnSn(SxSe1-x)4 (CZTSSe) films by solvent-free mechanochemical method and doctor blade process is described. First, CuS, ZnS and SnS nanoparticles are synthesized via a facile, solvent-free route, which is low cost and easy to scale-up. Second, the sulfides nanoparticulates precursors are deposited in a thin layer by doctor blade technique. Finally, the dry layers are sintered into CZTS/CZTSSe thin films. Different annealing processes are used, and the influences of incorporation of sulfur/selenium on the CZTS/CZTSSe films have been investigated. These structure, morphology and optical properties of CZTS/CZTSSe films are suitable for thin film solar cell fabrication.

  20. Controlled cadmium telluride thin films for solar cell applications (emerging materials systems for solar cell applications). Quarterly progress report No. 3, October 9, 1979-January 8, 1980

    SciTech Connect

    Vedam, K; Das, M B; Krishnaswamy, S V

    1980-02-01

    The main emphasis during the third quarter of the program was on the improvement of the quality of sputtered films, their characterization and use in the fabrication of Schottky barrier type diodes and solar cell structures. Films prepared under different conditions and on different substrates were examined by SEM showing nodular growths under certain conditions. I-V, C-V and photovoltaic characteristics were measured on numerous samples based on n- and p-type films on Ni substrates having top metallization of either evaporated Au and Al. The n-type samples showed up to 200mV V/sub oc/ and small short-circuit currents. The characteristics observed are indicative of the presence of interfacial layer and surface states. Surface state's capacitance were measured on p-type samples metallized with Au.

  1. Charge-Transfer Complexation at Carminic Acid-CdS Interface and Its Impact on the Efficiency of Dye-Sensitized Solar Cells

    NASA Astrophysics Data System (ADS)

    Shahzad, Naila; Shah, Syed Mujtaba; Munir, Shamsa; Hana, Amina; Jabeen, Uzma; Nosheen, Erum; Habib, Banafsha; Khan, Arif Ullah; Hassan, Zubair; Siddiq, Muhammad; Hussain, Hazrat

    2015-04-01

    We report for the first time charge-transfer complex formation at the interface of carminic acid and cadmium sulfide (CdS) nanoparticles. The complex formation was confirmed by ultraviolet-visible (UV-vis) and fluorescence emission spectroscopy. Cadmium sulfide nanoparticles were synthesized by the wet chemical method and characterized by UV-vis spectroscopy, x-ray diffraction and transmission electron microscopy. Carminic acid, in different concentrations, was chemisorbed on the surface of CdS nanoparticles. Grafting of carminic acid on CdS was confirmed by Fourier transform infrared spectroscopy. Energy levels of the highest occupied molecular orbitals and lowest unoccupied molecular orbitals (LUMO) of both carminic acid and CdS nanoparticles matched well for the injection of electron from LUMO of carminic acid to the conduction band of cadmium sulfide. The photoactive nanohybrid material was used in dye-sensitized solar cells. The efficiency of carminic acid functionalized CdS nanoparticles was found to be double the value obtained for the reference device and remained constant over a certain concentration range owing to the complex formation at the interface. However, raising the concentration of carminic acid beyond 2.5 × 10-5 M resulted in a decrease in efficiency. This was ascribed to charge recombination due to the presence of ungrafted carminic acid molecules.

  2. Insights into cadmium diffusion mechanisms in two-stage diffusion profiles in solar-grade Cu(In,Ga)Se{sub 2} thin films

    SciTech Connect

    Biderman, N. J.; Sundaramoorthy, R.; Haldar, Pradeep; Novak, Steven W.; Lloyd, J. R.

    2015-12-07

    Cadmium diffusion experiments were performed on polished copper indium gallium diselenide (Cu(In,Ga)Se{sub 2} or CIGS) samples with resulting cadmium diffusion profiles measured by time-of-flight secondary ion mass spectroscopy. Experiments done in the annealing temperature range between 275 °C and 425 °C reveal two-stage cadmium diffusion profiles which may be indicative of multiple diffusion mechanisms. Each stage can be described by the standard solutions of Fick's second law. The slower cadmium diffusion in the first stage can be described by the Arrhenius equation D{sub 1} = 3 × 10{sup −4} exp (− 1.53 eV/k{sub B}T) cm{sup 2} s{sup −1}, possibly representing vacancy-meditated diffusion. The faster second-stage diffusion coefficients determined in these experiments match the previously reported cadmium diffusion Arrhenius equation of D{sub 2} = 4.8 × 10{sup −4} exp (−1.04 eV/k{sub B}T) cm{sup 2} s{sup −1}, suggesting an interstitial-based mechanism.

  3. Insights into cadmium diffusion mechanisms in two-stage diffusion profiles in solar-grade Cu(In,Ga)Se2 thin films

    NASA Astrophysics Data System (ADS)

    Biderman, N. J.; Novak, Steven W.; Sundaramoorthy, R.; Haldar, Pradeep; Lloyd, J. R.

    2015-12-01

    Cadmium diffusion experiments were performed on polished copper indium gallium diselenide (Cu(In,Ga)Se2 or CIGS) samples with resulting cadmium diffusion profiles measured by time-of-flight secondary ion mass spectroscopy. Experiments done in the annealing temperature range between 275 °C and 425 °C reveal two-stage cadmium diffusion profiles which may be indicative of multiple diffusion mechanisms. Each stage can be described by the standard solutions of Fick's second law. The slower cadmium diffusion in the first stage can be described by the Arrhenius equation D1 = 3 × 10-4 exp (- 1.53 eV/kBT) cm2 s-1, possibly representing vacancy-meditated diffusion. The faster second-stage diffusion coefficients determined in these experiments match the previously reported cadmium diffusion Arrhenius equation of D2 = 4.8 × 10-4 exp (-1.04 eV/kBT) cm2 s-1, suggesting an interstitial-based mechanism.

  4. Cadmium carcinogenesis in review.

    PubMed

    Waalkes, M P

    2000-04-01

    Cadmium is an inorganic toxicant of great environmental and occupational concern which was classified as a human carcinogen in 1993. Occupational cadmium exposure is associated with lung cancer in humans. Cadmium exposure has also, on occasion, been linked to human prostate cancer. The epidemiological data linking cadmium and pulmonary cancer are much stronger than for prostatic cancer. Other target sites for cadmium carcinogenesis in humans (liver, kidney, stomach) are considered equivocal. In rodents, cadmium causes tumors at several sites and by various routes. Cadmium inhalation in rats results in pulmonary adenocarcinomas, supporting a role in human lung cancer. Prostate tumors and preneoplastic proliferative lesions can be induced in rats after cadmium ingestion or injection. Prostatic carcinogenesis in rats occurs only at cadmium doses below those that induce chronic degeneration and dysfunction of the testes, a well-known effect of cadmium, confirming the androgen dependency of prostate tumors. Other targets of cadmium in rodents include the testes, adrenals, injection sites, and hematopoietic system. Various treatments can modify cadmium carcinogenesis including supplemental zinc, which prevents cadmium-induced injection site and testicular tumors while facilitating prostatic tumors. Cadmium is poorly mutagenic and probably acts through indirect mechanisms, although the precise mechanisms remain unknown. PMID:10830873

  5. Cadmium carcinogenesis in review.

    PubMed

    Waalkes, M P

    2000-04-01

    Cadmium is an inorganic toxicant of great environmental and occupational concern which was classified as a human carcinogen in 1993. Occupational cadmium exposure is associated with lung cancer in humans. Cadmium exposure has also, on occasion, been linked to human prostate cancer. The epidemiological data linking cadmium and pulmonary cancer are much stronger than for prostatic cancer. Other target sites for cadmium carcinogenesis in humans (liver, kidney, stomach) are considered equivocal. In rodents, cadmium causes tumors at several sites and by various routes. Cadmium inhalation in rats results in pulmonary adenocarcinomas, supporting a role in human lung cancer. Prostate tumors and preneoplastic proliferative lesions can be induced in rats after cadmium ingestion or injection. Prostatic carcinogenesis in rats occurs only at cadmium doses below those that induce chronic degeneration and dysfunction of the testes, a well-known effect of cadmium, confirming the androgen dependency of prostate tumors. Other targets of cadmium in rodents include the testes, adrenals, injection sites, and hematopoietic system. Various treatments can modify cadmium carcinogenesis including supplemental zinc, which prevents cadmium-induced injection site and testicular tumors while facilitating prostatic tumors. Cadmium is poorly mutagenic and probably acts through indirect mechanisms, although the precise mechanisms remain unknown.

  6. Metal Sulfides as Sensing Materials for Chemoresistive Gas Sensors

    PubMed Central

    Gaiardo, Andrea; Fabbri, Barbara; Guidi, Vincenzo; Bellutti, Pierluigi; Giberti, Alessio; Gherardi, Sandro; Vanzetti, Lia; Malagù, Cesare; Zonta, Giulia

    2016-01-01

    This work aims at a broad overview of the results obtained with metal-sulfide materials in the field of chemoresistive gas sensing. Indeed, despite the well-known electrical, optical, structural and morphological features previously described in the literature, metal sulfides present lack of investigation for gas sensing applications, a field in which the metal oxides still maintain a leading role owing to their high sensitivity, low cost, small dimensions and simple integration, in spite of the wide assortment of sensing materials. However, despite their great advantages, metal oxides have shown significant drawbacks, which have led to the search for new materials for gas sensing devices. In this work, Cadmium Sulfide and Tin (IV) Sulfide were investigated as functional materials for thick-film chemoresistive gas-sensors fabrication and they were tested both in thermo- and in photo-activation modes. Furthermore, electrical characterization was carried out in order to verify their gas sensing properties and material stability, by comparing the results obtained with metal sulfides to those obtained by using their metal-oxides counterparts. The results highlighted the possibility to use metal sulfides as a novel class of sensing materials, owing to their selectivity to specific compounds, stability, and the possibility to operate at room temperature. PMID:26927120

  7. Metal Sulfides as Sensing Materials for Chemoresistive Gas Sensors.

    PubMed

    Gaiardo, Andrea; Fabbri, Barbara; Guidi, Vincenzo; Bellutti, Pierluigi; Giberti, Alessio; Gherardi, Sandro; Vanzetti, Lia; Malagù, Cesare; Zonta, Giulia

    2016-01-01

    This work aims at a broad overview of the results obtained with metal-sulfide materials in the field of chemoresistive gas sensing. Indeed, despite the well-known electrical, optical, structural and morphological features previously described in the literature, metal sulfides present lack of investigation for gas sensing applications, a field in which the metal oxides still maintain a leading role owing to their high sensitivity, low cost, small dimensions and simple integration, in spite of the wide assortment of sensing materials. However, despite their great advantages, metal oxides have shown significant drawbacks, which have led to the search for new materials for gas sensing devices. In this work, Cadmium Sulfide and Tin (IV) Sulfide were investigated as functional materials for thick-film chemoresistive gas-sensors fabrication and they were tested both in thermo- and in photo-activation modes. Furthermore, electrical characterization was carried out in order to verify their gas sensing properties and material stability, by comparing the results obtained with metal sulfides to those obtained by using their metal-oxides counterparts. The results highlighted the possibility to use metal sulfides as a novel class of sensing materials, owing to their selectivity to specific compounds, stability, and the possibility to operate at room temperature. PMID:26927120

  8. Metal Sulfides as Sensing Materials for Chemoresistive Gas Sensors.

    PubMed

    Gaiardo, Andrea; Fabbri, Barbara; Guidi, Vincenzo; Bellutti, Pierluigi; Giberti, Alessio; Gherardi, Sandro; Vanzetti, Lia; Malagù, Cesare; Zonta, Giulia

    2016-02-26

    This work aims at a broad overview of the results obtained with metal-sulfide materials in the field of chemoresistive gas sensing. Indeed, despite the well-known electrical, optical, structural and morphological features previously described in the literature, metal sulfides present lack of investigation for gas sensing applications, a field in which the metal oxides still maintain a leading role owing to their high sensitivity, low cost, small dimensions and simple integration, in spite of the wide assortment of sensing materials. However, despite their great advantages, metal oxides have shown significant drawbacks, which have led to the search for new materials for gas sensing devices. In this work, Cadmium Sulfide and Tin (IV) Sulfide were investigated as functional materials for thick-film chemoresistive gas-sensors fabrication and they were tested both in thermo- and in photo-activation modes. Furthermore, electrical characterization was carried out in order to verify their gas sensing properties and material stability, by comparing the results obtained with metal sulfides to those obtained by using their metal-oxides counterparts. The results highlighted the possibility to use metal sulfides as a novel class of sensing materials, owing to their selectivity to specific compounds, stability, and the possibility to operate at room temperature.

  9. Sulfide Mineralogy and Geochemistry

    NASA Astrophysics Data System (ADS)

    Dilles, John

    2007-02-01

    Reviews in Mineralogy and Geochemistry Series, Volume 61 David J. Vaughan, Editor Geochemical Society and Mineralogical Society of America; ISBN 0-939950-73-1 xiii + 714 pp.; 2006; $40. Sulfide minerals as a class represent important minor rock-forming minerals, but they are generally known as the chief sources of many economic metallic ores. In the past two decades, sulfide research has been extended to include important roles in environmental geology of sulfide weathering and resultant acid mine drainage, as well as in geomicrobiology in which bacteria make use of sulfides for metabolic energy sources. In the latter respect, sulfides played an important role in early evolution of life on Earth and in geochemical cycling of elements in the Earth's crust and hydrosphere.

  10. CdS: Characterization and recent advances in CdTe solar cell performance

    SciTech Connect

    Ferekides, C.; Marinskiy, D.; Morel, D.L.

    1997-12-31

    Cadmium sulfide (CdS) films deposited by chemical bath deposition (CBD) have been used for the fabrication of high efficiency CdTe and CuIn{sub 1{minus}x}Ga{sub x}Se{sub 2} thin film solar cells. An attractive alternative deposition technology with manufacturing advantages over the CBD is the close spaced sublimation (CSS). In this work CdTe/CdS solar cells prepared entirely by the CSS process exhibited 15.0% efficiencies under global AM1.5 conditions as verified at the National Renewable Energy Laboratory. This paper reports on studies carried out on as deposited and heat treated CSS CdS films and all CSS CdTe/CdS solar cells using photoluminescence, x-ray diffraction, and I-V-T measurements.

  11. Bioremediation of cadmium by growing Rhodobacter sphaeroides: kinetic characteristic and mechanism studies.

    PubMed

    Bai, Hong-Juan; Zhang, Zhao-Ming; Yang, Guan-E; Li, Bao-Zhen

    2008-11-01

    The removal kinetic characteristic and mechanism of cadmium by growing Rhodobacter sphaeroides were investigated. The removal data were fitted to the second-order equation, with a correlation coefficient, R2=0.9790-0.9916. Furthermore, it was found that the removal mechanism of cadmium was predominantly governed by bioprecipitation as cadmium sulfide with biosorption contributing to a minor extent. Also, the results revealed that the activities of cysteine desulfhydrase in strains grown in the presence of 10 and 20 mg/l of cadmium were higher than in the control, while the activities in the presence of 30 and 40 mg/l of cadmium were lower than in the control. Content analysis of subcellular fractionation showed that cadmium was mostly removed and transformed by precipitation on the cell wall.

  12. Process for fabricating polycrystalline semiconductor thin-film solar cells, and cells produced thereby

    DOEpatents

    Wu, Xuanzhi; Sheldon, Peter

    2000-01-01

    A novel, simplified method for fabricating a thin-film semiconductor heterojunction photovoltaic device includes initial steps of depositing a layer of cadmium stannate and a layer of zinc stannate on a transparent substrate, both by radio frequency sputtering at ambient temperature, followed by the depositing of dissimilar layers of semiconductors such as cadmium sulfide and cadmium telluride, and heat treatment to convert the cadmium stannate to a substantially single-phase material of a spinel crystal structure. Preferably, the cadmium sulfide layer is also deposited by radio frequency sputtering at ambient temperature, and the cadmium telluride layer is deposited by close space sublimation at an elevated temperature effective to convert the amorphous cadmium stannate to the polycrystalline cadmium stannate with single-phase spinel structure.

  13. Mechanisms of Cadmium Carcinogenesis

    EPA Science Inventory

    Cadmium is a transition metal and an ubiquitous environmental and industrial pollutant. Laboratory animal studies and epidemiological studies have shown that exposure to cadmium is associated with various organ toxicities and carcinogenic effects. Several national and internation...

  14. Process for removing and detoxifying cadmium from scrap metal including mixed waste

    SciTech Connect

    Kronberg, J.W.

    1994-07-01

    Cadmium-bearing scrap from nuclear applications, such as neutron shielding and reactor control and safety rods, must usually be handled as mixed waste since it is radioactive and the cadmium in it is both leachable and highly toxic. Removing the cadmium from this scrap, and converting it to a nonleachable and minimally radioactive form, would greatly simplify disposal or recycling. A process now under development will do this by shredding the scrap; leaching it with reagents which selectively dissolve out the cadmium; reprecipitating the cadmium as its highly insoluble sulfide; then fusing the sulfide into a glassy matrix to bring its leachability below EPA limits before disposal. Alternatively, the cadmium may be recovered for reuse. A particular advantage of the process is that all reagents (except the glass frit) can easily be recovered and reused in a nearly closed cycle, minimizing the risk of radioactive release. The process does not harm common metals such as aluminum, iron and stainless steel, and is also applicable to non-nuclear cadmium-bearing scrap such as nickel-cadmium batteries.

  15. Facile room-temperature synthesis of carboxylated graphene oxide-copper sulfide nanocomposite with high photodegradation and disinfection activities under solar light irradiation

    NASA Astrophysics Data System (ADS)

    Yu, Shuyan; Liu, Jincheng; Zhu, Wenyu; Hu, Zhong-Ting; Lim, Teik-Thye; Yan, Xiaoli

    2015-11-01

    Carboxylic acid functionalized graphene oxide-copper (II) sulfide nanoparticle composite (GO-COOH-CuS) was prepared from carboxylated graphene oxide and copper precursor in dimethyl sulfoxide (DMSO) by a facile synthesis process at room temperature. The high-effective combination, the interaction between GO-COOH sheets and CuS nanoparticles, and the enhanced visible light absorption were confirmed by transmission electron microscopy (TEM), field emission scanning electron microscopy (FESEM), X-ray powder diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), thermo gravimetric analysis (TGA), X-ray photoelectron spectroscopy (XPS), UV-vis diffuse reflectance spectra (DRS) and Photoluminescence (PL) spectra. The as-synthesized GO-COOH-CuS nanocomposite exhibited excellent photocatalytic degradation performance of phenol and rhodamine B, high antibacterial activity toward E. coli and B. subtilis, and good recovery and reusability. The influence of CuS content, the synergistic reaction between CuS and GO-COOH, and the charge-transfer mechanism were systematically investigated. The facile and low-energy synthesis process combined with the excellent degradation and antibacterial performance signify that the GO-COOH-CuS has a great potential for water treatment application.

  16. A Two-Step Absorber Deposition Approach To Overcome Shunt Losses in Thin-Film Solar Cells: Using Tin Sulfide as a Proof-of-Concept Material System.

    PubMed

    Steinmann, Vera; Chakraborty, Rupak; Rekemeyer, Paul H; Hartman, Katy; Brandt, Riley E; Polizzotti, Alex; Yang, Chuanxi; Moriarty, Tom; Gradečak, Silvija; Gordon, Roy G; Buonassisi, Tonio

    2016-08-31

    As novel absorber materials are developed and screened for their photovoltaic (PV) properties, the challenge remains to reproducibly test promising candidates for high-performing PV devices. Many early-stage devices are prone to device shunting due to pinholes in the absorber layer, producing "false-negative" results. Here, we demonstrate a device engineering solution toward a robust device architecture, using a two-step absorber deposition approach. We use tin sulfide (SnS) as a test absorber material. The SnS bulk is processed at high temperature (400 °C) to stimulate grain growth, followed by a much thinner, low-temperature (200 °C) absorber deposition. At a lower process temperature, the thin absorber overlayer contains significantly smaller, densely packed grains, which are likely to provide a continuous coating and fill pinholes in the underlying absorber bulk. We compare this two-step approach to the more standard approach of using a semi-insulating buffer layer directly on top of the annealed absorber bulk, and we demonstrate a more than 3.5× superior shunt resistance Rsh with smaller standard error σRsh. Electron-beam-induced current (EBIC) measurements indicate a lower density of pinholes in the SnS absorber bulk when using the two-step absorber deposition approach. We correlate those findings to improvements in the device performance and device performance reproducibility.

  17. Facile room-temperature synthesis of carboxylated graphene oxide-copper sulfide nanocomposite with high photodegradation and disinfection activities under solar light irradiation

    PubMed Central

    Yu, Shuyan; Liu, Jincheng; Zhu, Wenyu; Hu, Zhong-Ting; Lim, Teik-Thye; Yan, Xiaoli

    2015-01-01

    Carboxylic acid functionalized graphene oxide-copper (II) sulfide nanoparticle composite (GO-COOH-CuS) was prepared from carboxylated graphene oxide and copper precursor in dimethyl sulfoxide (DMSO) by a facile synthesis process at room temperature. The high-effective combination, the interaction between GO-COOH sheets and CuS nanoparticles, and the enhanced visible light absorption were confirmed by transmission electron microscopy (TEM), field emission scanning electron microscopy (FESEM), X-ray powder diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), thermo gravimetric analysis (TGA), X-ray photoelectron spectroscopy (XPS), UV-vis diffuse reflectance spectra (DRS) and Photoluminescence (PL) spectra. The as-synthesized GO-COOH-CuS nanocomposite exhibited excellent photocatalytic degradation performance of phenol and rhodamine B, high antibacterial activity toward E. coli and B. subtilis, and good recovery and reusability. The influence of CuS content, the synergistic reaction between CuS and GO-COOH, and the charge-transfer mechanism were systematically investigated. The facile and low-energy synthesis process combined with the excellent degradation and antibacterial performance signify that the GO-COOH-CuS has a great potential for water treatment application. PMID:26553709

  18. A Two-Step Absorber Deposition Approach To Overcome Shunt Losses in Thin-Film Solar Cells: Using Tin Sulfide as a Proof-of-Concept Material System.

    PubMed

    Steinmann, Vera; Chakraborty, Rupak; Rekemeyer, Paul H; Hartman, Katy; Brandt, Riley E; Polizzotti, Alex; Yang, Chuanxi; Moriarty, Tom; Gradečak, Silvija; Gordon, Roy G; Buonassisi, Tonio

    2016-08-31

    As novel absorber materials are developed and screened for their photovoltaic (PV) properties, the challenge remains to reproducibly test promising candidates for high-performing PV devices. Many early-stage devices are prone to device shunting due to pinholes in the absorber layer, producing "false-negative" results. Here, we demonstrate a device engineering solution toward a robust device architecture, using a two-step absorber deposition approach. We use tin sulfide (SnS) as a test absorber material. The SnS bulk is processed at high temperature (400 °C) to stimulate grain growth, followed by a much thinner, low-temperature (200 °C) absorber deposition. At a lower process temperature, the thin absorber overlayer contains significantly smaller, densely packed grains, which are likely to provide a continuous coating and fill pinholes in the underlying absorber bulk. We compare this two-step approach to the more standard approach of using a semi-insulating buffer layer directly on top of the annealed absorber bulk, and we demonstrate a more than 3.5× superior shunt resistance Rsh with smaller standard error σRsh. Electron-beam-induced current (EBIC) measurements indicate a lower density of pinholes in the SnS absorber bulk when using the two-step absorber deposition approach. We correlate those findings to improvements in the device performance and device performance reproducibility. PMID:27494110

  19. Design of pilot-scale solar photocatalytic reactor for the generation of hydrogen from alkaline sulfide wastewater of sewage treatment plant.

    PubMed

    Priya, R; Kanmani, S

    2013-01-01

    Experiments were conducted for photocatalytic generation of renewable fuel hydrogen from sulphide wastewater from the sewage treatment plant. In this study, pilot-scale solar photocatalytic reactor was designed for treating 1 m3 of sulphide wastewater and also for the simultaneous generation of hydrogen. Bench-scale studies were conducted both in the batch recycle and continuous modes under solar irradiation at similar experimental conditions. The maximum of 89.7% conversion was achieved in the continuous mode. The length of the pilot-scale solar photocatalytic reactor was arrived using the design parameters such as volumetric flow rate (Q) (11 x 10(-2) m3/s), inlet concentration of sulphide ion (C(in)) (28 mol/m3), conversion (89.7%) and average mass flow destruction rate (3.488 x 10(-6) mol/m2 s). The treatment cost of the process was estimated to be 6 US$/m3. This process would be suitable for India like sub-tropical country where sunlight is abundantly available throughout the year.

  20. Cadmium and renal cancer

    SciTech Connect

    Il'yasova, Dora; Schwartz, Gary G. . E-mail: gschwart@wfubmc.edu

    2005-09-01

    Background: Rates of renal cancer have increased steadily during the past two decades, and these increases are not explicable solely by advances in imaging modalities. Cadmium, a widespread environmental pollutant, is a carcinogen that accumulates in the kidney cortex and is a cause of end-stage renal disease. Several observations suggest that cadmium may be a cause of renal cancer. Methods: We performed a systematic review of the literature on cadmium and renal cancer using MEDLINE for the years 1966-2003. We reviewed seven epidemiological and eleven clinical studies. Results: Despite different methodologies, three large epidemiologic studies indicate that occupational exposure to cadmium is associated with increased risk renal cancer, with odds ratios varying from 1.2 to 5.0. Six of seven studies that compared the cadmium content of kidneys from patients with kidney cancer to that of patients without kidney cancer found lower concentrations of cadmium in renal cancer tissues. Conclusions: Exposure to cadmium appears to be associated with renal cancer, although this conclusion is tempered by the inability of studies to assess cumulative cadmium exposure from all sources including smoking and diet. The paradoxical findings of lower cadmium content in kidney tissues from patients with renal cancer may be caused by dilution of cadmium in rapidly dividing cells. This and other methodological problems limit the interpretation of studies of cadmium in clinical samples. Whether cadmium is a cause of renal cancer may be answered more definitively by future studies that employ biomarkers of cadmium exposure, such as cadmium levels in blood and urine.

  1. Evaluation of the potential carcinogenicity of cadmium, cadium acetate, cadmium bromide, cadmium chloride. Final report

    SciTech Connect

    Not Available

    1988-06-01

    Cadmium is a probable human carcinogen, classified as weight-of-evidence Group B1 under the EPA Guidelines for Carcinogen Risk Assessment (U.S. EPA, 1986a). Evidence on potential carcinogenicity from animal studies is Sufficient, and the evidence from human studies is Limited. The potency factor (F) for cadmium is estimated to be 57.9/(mg/kg/day) (based on epidemiology data for cadmium workers), placing it in potency group 2 according to the CAG's methodology for evaluating potential carcinogens (U.S. EPA, 1986b). Cadmium weight of evidence and potency are based on epidemiology data for cadmium workers exposed to cadmium oxide and/or cadmium fume. Although human data for cadmium salts are lacking, due to the responsiveness of animals to soluble cadmium compounds, especially cadmium chloride, the weight of evidence and potency for cadmium acetate, cadmium bromide and cadmium chloride are considered to be the same as those cadmium compounds to which workers are exposed. Thus, cadmium acetate, cadmium bromide, and cadmium chloride are all classified as weight-of-evidence Group and the potency group, cadmium, cadmium acetate, cadmium bromide, and cadmium chloride are assigned MEDIUM hazard rankings for the purposes of RQ adjustment. Combining the weight-of-evidence group and the potency group, carbon tetrachloride is assigned a MEDIUM hazard ranking for the purposes of RQ adjustment.

  2. Framework to predict optimal buffer layer pairing for thin film solar cell absorbers: A case study for tin sulfide/zinc oxysulfide

    SciTech Connect

    Mangan, Niall M.; Brandt, Riley E.; Steinmann, Vera; Jaramillo, R.; Poindexter, Jeremy R.; Chakraborty, Rupak; Buonassisi, Tonio; Yang, Chuanxi; Park, Helen Hejin; Zhao, Xizhu; Gordon, Roy G.

    2015-09-21

    An outstanding challenge in the development of novel functional materials for optoelectronic devices is identifying suitable charge-carrier contact layers. Herein, we simulate the photovoltaic device performance of various n-type contact material pairings with tin(II) sulfide (SnS), a p-type absorber. The performance of the contacting material, and resulting device efficiency, depend most strongly on two variables: conduction band offset between absorber and contact layer, and doping concentration within the contact layer. By generating a 2D contour plot of device efficiency as a function of these two variables, we create a performance-space plot for contacting layers on a given absorber material. For a simulated high-lifetime SnS absorber, this 2D performance-space illustrates two maxima, one local and one global. The local maximum occurs over a wide range of contact-layer doping concentrations (below 10{sup 16 }cm{sup −3}), but only a narrow range of conduction band offsets (0 to −0.1 eV), and is highly sensitive to interface recombination. This first maximum is ideal for early-stage absorber research because it is more robust to low bulk-minority-carrier lifetime and pinholes (shunts), enabling device efficiencies approaching half the Shockley-Queisser limit, greater than 16%. The global maximum is achieved with contact-layer doping concentrations greater than 10{sup 18 }cm{sup −3}, but for a wider range of band offsets (−0.1 to 0.2 eV), and is insensitive to interface recombination. This second maximum is ideal for high-quality films because it is more robust to interface recombination, enabling device efficiencies approaching the Shockley-Queisser limit, greater than 20%. Band offset measurements using X-ray photoelectron spectroscopy and carrier concentration approximated from resistivity measurements are used to characterize the zinc oxysulfide contacting layers in recent record-efficiency SnS devices. Simulations representative of these

  3. Retrospective mortality study of cadmium workers: An update

    SciTech Connect

    Thun, M.J.; Schnorr, T.M.; Halperin, W.E.

    1986-02-06

    A retrospective cohort mortality study was conducted among a group of workers exposed to cadmium (7440439), to determine specific causes of death among these workers. The report reviewed the findings of the study and presented additional findings concerning exposures to other hazards at the facility. The study examined the causes of death for 292 cadmium workers who worked at least 2 years at a small facility that recovered cadmium from bag house dust. Exposures included dusts of cadmium-oxide (1306190) and cadmium-sulfide (1306236) and to fumes of cadmium itself. Over a two fold excess of deaths from respiratory cancer was noted among these workers when compared with the general population and over a three fold excess of deaths from prostatic cancer among the men. A follow up of the study cohort revealed that all cause mortality was slightly below that of the United States male population. The Standardized Mortality Ratio for circulatory disease was 65. Deaths due to respiratory cancer were 65% above the number expected. All of the 20 deaths from respiratory cancer were due to cancer of the lung, trachea and bronchus. Deaths due to genitourinary cancer were 35% above expected levels.

  4. Thioarsenates in sulfidic waters.

    PubMed

    Stauder, S; Raue, B; Sacher, F

    2005-08-15

    It has long been recognized that the formation of soluble arsenic sulfur complexes plays a key role for the mobility and toxicity of arsenic in sulfate-reducing environments. Knowledge of the exact arsenic species is essential to understand the behavior of arsenic in sulfidic aquifers and to develop remediation strategies. In the past, monomeric and trimeric thioarsenites were assumed to be the existing species in sulfidic systems. In this study, thioarsenates were identified by IC-ICP/MS in arsenite- and sulfide-containing solutions as well as in a reduced groundwater from a contaminated site. The unexpected finding of an oxidation of As(lll) to As(V) in thioarsenates in strongly reducing systems can be explained by the high affinity between As(Ill) and sulfur. In sulfide-containing solutions without oxidant, As(lll) therefore undergoes disproportionation to thioarsenates (As(V)) and elemental arsenic. It has previously been supposed that mobility as well as toxicity of arsenic increases if the redox state decreases. For sulfidic waters, the opposite is probably the case. Thus, the formation of thioarsenates could be used in connection with remediation strategies. Thioarsenates are highly sensitive to oxygen and pH. This is important for analytical procedures. A loss of soluble arsenic as well as a conversion to arsenite and arsenate may occur if water samples containing thioarsenates are analyzed with conventional methods.

  5. Enhancement of Photo-Current Conversion Efficiency in a CdS/CdSe Quantum-Dot-Sensitized Solar Cell Incorporated with Single-Walled Carbon Nanotubes.

    PubMed

    Park, Hyunjune; Lee, Jongtaek; Park, Taehee; Lee, Sanghun; Yi, Whikun

    2015-02-01

    Cadmium sulfide (CdS) and cadmium selenide (CdSe) are sequentially assembled onto a nanocrystalline TiO2 film to create a quantum-dot (QD)-sensitized solar cell application by a successive ionic layer adsorption and reaction (SILAR) method. The results show that CdS and CdSe QDs have a complementary effect in the performance of light harvest of solar cell. Single-walled carbon nanotubes (SWNTs) are incorporated with a CdS/CdSe QDs solar cell by mixing them with TiC2 film to enhance electron transfer. SWNTs are also sprayed onto CdSe QDs (SWNTs onto CdSe) to apply p+ type properties of SWNTs. Absorbance is increased in a wide wavelength range. In particular, cells having the sprayed SWNTs onto the QDs show a clear increase in absorbance at a low wavelength region. The fill factor of CdS/CdSe QDs solar cell with SWNTs is higher than that without SWNTs, indicating the decrease in loss of electron from TiO2 to QDs. Short-circuit current in a QD-sensitized solar cell having SWNTs on CdSe shows maximum value. Photo-current conversion efficiency of cells is increased in both cell types containing SWNTs at 10~17% compared with pristine cells. We expect that solar cells using SWNTs will affect future energy technology and devices.

  6. Preparation of SnS/CdS Co-sensitized TiO2 Photoelectrodes for Quantum Dots Sensitized Solar Cells

    NASA Astrophysics Data System (ADS)

    Xie, Yu-Long; Song, Ping; Zhao, Su-Qing

    2016-10-01

    TiO2 porous films have been prepared by electrophoresis deposition method, while tin sulfide (SnS) and cadmium sulfide quantum dots (QDs) have been deposited by a simple and inexpensive successive ionic layer adsorption and reaction method. The CdS and SnS QDs modifications expanded the photoresponse range of TiO2 nanoparticles from the ultraviolet region to visible range. Such prepared SnS/CdS/TiO2 films were used as photo-anodes to assemble QDs sensitized solar cells with I-/I3 - liquid electrolyte and Pt-coated fluorine-doped tin oxide glass counter electrode. The best resulting cells had an open circuit voltage of 520 mV, a short circuit current density of 2.972 mA cm-2, a fill factor of 0.61, and with a conversion efficiency of 0.936%.

  7. Sulfidation of silver nanoparticles

    NASA Astrophysics Data System (ADS)

    Levard, C.; Michel, F. M.; Brown, G. E.

    2010-12-01

    Rapid development of nanotechnologies that exploit the properties of silver nanoparticles (Ag-NPs) raises questions concerning the impact of Ag on the environment. Ag-NPs are currently among the most widely used in the nanotechnology industry and the amount released into the environment is expected to increase along with production (1). When present in geochemical systems, Ag-NPs may undergo a variety of changes due to varying redox, pH, and chemical conditions. Expected changes range from surface modification (e.g., oxidation, sulfidation, chloridation etc.) to complete dissolution and re-precipitation. In this context, the focus of our work is on understanding the behavior of synthetic Ag-NPs with different particle sizes under varying conditions relevant to the environment. Sulfidation of Ag-NPs is of particular interest since it among the processes most likely to occur in aqueous systems, in particular under reducing conditions. Three sizes of Ag-NPs coated with polyvinyl pyrrolidone were produced using the polyol process (2) (7 ±1; 20 ±4, and 40 ±9 nm). Batch solutions containing the different Ag-NPs were subsequently reacted with Na2S solutions of different concentrations. The sulfidation process was followed step-wise for 24 hours and the corrosion products formed were characterized by electron microscopy (TEM/SEM), diffraction (XRD), and photo-electron spectroscopy (XPS). Surface charge (pHPZC) of the products formed during this process was also measured, as were changes in solubility and reactivity. Based on experimental observations we infer that the sulfidation process is the result of dissolution-precipitation and find that: (i) acanthite (Ag2S) is formed as a corrosion product; (ii) Ag-NPs aggregation increased with sulfidation rate; (iii) pHPZC increases with the rate of sulfidation; and (iv) the solubility of the corrosion products formed from sulfidation appears lower than that of non-sulfidated Ag-NPs. We observe size-dependent differences in

  8. Electron Microscopy Study of Exotic Nanostructures of Cadmium Sulfide

    NASA Astrophysics Data System (ADS)

    Dong, Lifeng; Jiao, Jun

    2005-04-01

    In this article, two simple methods, evaporation-condensation and catalytic thermal evaporation, were used to investigate the synthesis of CdS nanostructures for nanoscale optoelectronic applications. To understand their growth mechanisms, various electron microscopy and microanalysis techniques were utilized in characterizing their morphologies, internal structures, growth directions and elemental compositions. The electron microscopy study reveals that when using the evaporation-condensation method, branched CdS nanorods and self-assembled arrays of CdS nanorods were synthesized at 800°C and 1000°C, respectively. Instead of morphological differences, both types of CdS nanorods grew along the [0001] direction. However, when using the catalytic thermal evaporation method (Au as the catalyst), patterned CdS nanowires and nanobelts were formed at the temperature region of 500 600°C and 600 750°C, respectively. Their growth direction was along the direction [1010] instead of [0001]. Based on the microscopy and microanalysis results, we propose some growth mechanisms in relation to the growth processes of those exotic CdS nanostructures.

  9. SULFIDE METHOD PLUTONIUM SEPARATION

    DOEpatents

    Duffield, R.B.

    1958-08-12

    A process is described for the recovery of plutonium from neutron irradiated uranium solutions. Such a solution is first treated with a soluble sullide, causing precipitation of the plutoniunn and uraniunn values present, along with those impurities which form insoluble sulfides. The precipitate is then treated with a solution of carbonate ions, which will dissolve the uranium and plutonium present while the fission product sulfides remain unaffected. After separation from the residue, this solution may then be treated by any of the usual methods, such as formation of a lanthanum fluoride precipitate, to effect separation of plutoniunn from uranium.

  10. Cadmium - a metallohormone?

    PubMed Central

    Byrne, Celia; Divekar, Shailaja D.; Storchan, Geoffrey B.; Parodi, Daniela A.; Martin, Mary Beth

    2009-01-01

    Cadmium is a heavy metal that is often referred to as the metal of the 20th Century. It is widely used in industry principally in galvanizing and electroplating, in batteries, in electrical conductors, in the manufacture of alloys, pigments, and plastics, and in the stabilization of phosphate fertilizers. As a byproduct of smelters, cadmium is a prevalent environmental contaminant. In the general population, exposure to cadmium occurs primarily through dietary sources, cigarette smoking, and, to a lesser degree, drinking water. Although the metal has no known physiological function, there is evidence to suggest that the cadmium is a potent metallohormone. This review summarizes the increasing evidence that cadmium mimics the function of steroid hormones, addresses our current understanding of the mechanism by which cadmium functions as a hormone, and discusses its potential role in development of the hormone dependent cancers. PMID:19362102

  11. Cadmium in tobacco

    SciTech Connect

    Yue, L. )

    1992-03-01

    The present study was conducted to determine the cadmium level in tobacco planted in five main tobacco-producing areas, a cadmium polluted area, and in cigarettes produced domestically (54 brands). The results indicate that average cadmium content in tobacco was 1.48 (0.10-4.95 mg/kg), which was similar to that of Indian tobacco (1.24 mg/kg), but the cadmium of tobacco produced in the cadmium polluted area was quite high (8.60 mg/kg). The average cigarette cadmium was 1.05 micrograms/g (with filter tip) and 1.61 micrograms/g (regular cigarette). Therefore special attention should be paid to the soil used in planting tobacco.

  12. Cadmium - A metallohormone?

    SciTech Connect

    Byrne, Celia; Divekar, Shailaja D.; Storchan, Geoffrey B.; Parodi, Daniela A.; Martin, Mary Beth

    2009-08-01

    Cadmium is a heavy metal that is often referred to as the metal of the 20th century. It is widely used in industry principally in galvanizing and electroplating, in batteries, in electrical conductors, in the manufacture of alloys, pigments, and plastics, and in the stabilization of phosphate fertilizers. As a byproduct of smelters, cadmium is a prevalent environmental contaminant. In the general population, exposure to cadmium occurs primarily through dietary sources, cigarette smoking, and, to a lesser degree, drinking water. Although the metal has no known physiological function, there is evidence to suggest that the cadmium is a potent metallohormone. This review summarizes the increasing evidence that cadmium mimics the function of steroid hormones, addresses our current understanding of the mechanism by which cadmium functions as a hormone, and discusses its potential role in development of the hormone dependent cancers.

  13. Cadmium toxicity and treatment.

    PubMed

    Bernhoft, Robin A

    2013-01-01

    Cadmium is a heavy metal of considerable toxicity with destructive impact on most organ systems. It is widely distributed in humans, the chief sources of contamination being cigarette smoke, welding, and contaminated food and beverages. Toxic impacts are discussed and appear to be proportional to body burden of cadmium. Detoxification of cadmium with EDTA and other chelators is possible and has been shown to be therapeutically beneficial in humans and animals when done using established protocols.

  14. Cadmium Toxicity and Treatment

    PubMed Central

    Bernhoft, Robin A.

    2013-01-01

    Cadmium is a heavy metal of considerable toxicity with destructive impact on most organ systems. It is widely distributed in humans, the chief sources of contamination being cigarette smoke, welding, and contaminated food and beverages. Toxic impacts are discussed and appear to be proportional to body burden of cadmium. Detoxification of cadmium with EDTA and other chelators is possible and has been shown to be therapeutically beneficial in humans and animals when done using established protocols. PMID:23844395

  15. Zinc sulfide liquefaction catalyst

    DOEpatents

    Garg, Diwakar

    1984-01-01

    A process for the liquefaction of carbonaceous material, such as coal, is set forth wherein coal is liquefied in a catalytic solvent refining reaction wherein an activated zinc sulfide catalyst is utilized which is activated by hydrogenation in a coal derived process solvent in the absence of coal.

  16. Dip coated nanocrystalline CdZnS thin films for solar cell application

    SciTech Connect

    Dongre, J. K. Chaturvedi, Mahim; Patil, Yuvraj; Sharma, Sandhya; Jain, U. K.

    2015-07-31

    Nanocrystalline cadmium sulfide (CdS) and zinc cadmium sulfide (ZnCdS) thin films have been grown via simple and low cost dip coating technique. The prepared films are characterized by X-ray diffraction (XRD), atomic force microscopic (AFM) and UV-VIS spectrophotometer techniques to reveal their structural, morphological and optical properties. XRD shows that both samples grown have zinc blende structure. The grain size is calculated as 6.2 and 8 nm using Scherrer’s formula. The band gap value of CdS and CdZnS film is estimated to be 2.58 and 2.69 eV respectively by UV-vis spectroscopy. Photoelectrochemical (PEC) investigations are carried out using cell configuration as n-CdZnS/(1M NaOH + 1M Na2S + 1M S)/C. The photovoltaic output characteristic is used to calculate fill-factor (FF) and solar conversion efficiency (η)

  17. Wet oxidation of oil-bearing sulfide wastes

    SciTech Connect

    Miller, R.L.; Hotz, N.J.

    1991-01-01

    Oil-bearing metal sulfide sludges produced in treatment of an industrial wastewater, which includes plating wastes, have yielded to treatment by electrooxidation and hydrogen peroxide processes. The oxidation can be controlled to be mild enough to avoid decomposition of the organic phase while oxidizing the sulfides to sulfates. The pH is controlled to near neutral conditions where iron, aluminum and chromium(III) precipitate as hydrous oxides. Other metals, such as lead and barium, may be present as sulfate precipitates with limited solubility, while metals such as nickel and cadmium would be present as complexed ions in a sulfate solution. The oxidations were found to proceed smoothly, without vigorous reaction; heat liberation was minimal. 2 refs., 12 figs.

  18. Synthesis and photovoltaic application of coper (I) sulfide nanocrystals

    SciTech Connect

    Wu, Yue; Wadia, Cyrus; Ma, Wanli; Sadtler, Bryce; Alivisatos, A.Paul

    2008-06-24

    We present the rational synthesis of colloidal copper(I) sulfide nanocrystals and demonstrate their application as an active light absorbing component in combination with CdS nanorods to make a solution-processed solar cell with 1.6percent power conversion efficiency on both conventional glass substrates and flexible plastic substrates with stability over a 4 month testing period.

  19. Polycrystalline thin-film, cadmium-telluride solar cells fabricated by electrodeposition cells. Final subcontract report, March 20, 1992--April 27, 1995

    SciTech Connect

    Trefny, J.U.; Mao, D.; Kim, D.

    1995-10-01

    The objective of this project was to develop improved processes for the fabrication of CdTe/CdS polycrystalline thin film solar cells. The technique we used for the formation of CdTe, electrodeposition, was a non-vacuum, low-cost technique that is attractive for economic, large-scale production. Annealing effects and electrical properties are discussed.

  20. Cadmium in zinc deposits: Economic geology of a polluting element

    SciTech Connect

    Schwartz, M.O.

    2000-05-01

    The chief host of cadmium in zinc deposits is sphalerite, the cadmium content of which depends on the type of deposit. Sphalerite from Mississippi Valley-type (MVT) deposits has high cadmium concentrations whereas sphalerite from exhalative deposits has low cadmium concentrations. The Cd content of sphalerite depends on the Cd/Zn ratio, ligand activities, and temperature of the ore-forming fluids. The combined effect of variation of temperature, pH, total activity of reduced sulfur, and activity of Cl{sup {minus}} cannot by itself account for either Cd depletion (exhalative deposits) or Cd enrichment (MVT deposits). Variations in the Cd/Zn ratio of the fluid have a significant effect in determining that of sphalerite. Basinal brines, which can be considered to be the recent equivalents of MVT fluids, have high Cd/Zn ratios, and active exhalative systems are characterized by low Cd/Zn ratios. Probably the differences in sphalerite composition between the different deposit types are less a function of temperature and ligand activities than Cd/Zn ratio of the ore-forming fluids. In the hydrothermal environment, the Cd/Zn ratio is generally not high enough to allow crystallization of cadmium sulfides (greenockite or hawleyite). The abundance of greenockite in the supergene alteration zone of hydrothermal zinc deposits can be explained on the basis of Zn scavenging by crystallizing smithsonite.

  1. Electrochemical behavior of silver sulfide

    SciTech Connect

    Drouven, B.U.E.

    1982-01-01

    The electrochemical behavior of silver sulfide in sulfuric acid as well as in nitric acid was studied using electrodes made from synthetic silver sulfide. The primary techniques used were potentiostatic, potentiodynamic, galvanostatic and corrosion cell experiments. The cathodic reaction of silver sulfide produces silver and hydrogen sulfide. This reaction mechanism is a sequential two step charge transfer involving a single electron in each step. Silver ions are produced from silver sulfide upon applying an anodic potential. The dissolution rate of silver sulfide can be so high that the formation of silver sulfate occurs which partially covers the silver sulfide surface and inhibits a further rate increase. The sulfur from the silver sulfide will be oxidized at low overpotentials to elemental sulfur; at high overpotentials, the oxidation to sulfate or bisulfate is observed. The results suggest that the catalysis of chalcopyrite by the addition of silver ions is caused by the formation and subsequent dissolution of silver sulfide leaving a porous layer behind. The understanding of the reaction mechanism of silver sulfide dissolution and its optimization will significantly improve the economic evaluation of industrial processes using the catalyzed leaching of chalcopyrite. The present knowledge of the catalysis indicates that other ions may be substituted for silver ions which would increase the feasibility of hydrometallurgical processes.

  2. Sulfide detoxification in plant mitochondria.

    PubMed

    Birke, Hannah; Hildebrandt, Tatjana M; Wirtz, Markus; Hell, Rüdiger

    2015-01-01

    In contrast to animals, which release the signal molecule sulfide in small amounts from cysteine and its derivates, phototrophic eukaryotes generate sulfide as an essential intermediate of the sulfur assimilation pathway. Additionally, iron-sulfur cluster turnover and cyanide detoxification might contribute to the release of sulfide in mitochondria. However, sulfide is a potent inhibitor of cytochrome c oxidase in mitochondria. Thus, efficient sulfide detoxification mechanisms are required in mitochondria to ensure adequate energy production and consequently survival of the plant cell. Two enzymes have been recently described to catalyze sulfide detoxification in mitochondria of Arabidopsis thaliana, O-acetylserine(thiol)lyase C (OAS-TL C), and the sulfur dioxygenase (SDO) ethylmalonic encephalopathy protein 1 (ETHE1). Biochemical characterization of sulfide producing and consuming enzymes in mitochondria of plants is fundamental to understand the regulatory network that enables mitochondrial sulfide homeostasis under nonstressed and stressed conditions. In this chapter, we provide established protocols to determine the activity of the sulfide releasing enzyme β-cyanoalanine synthase as well as sulfide-consuming enzymes OAS-TL and SDO. Additionally, we describe a reliable and efficient method to purify OAS-TL proteins from plant material.

  3. Cadmium sulfide-copper sulfide heterojunction cell research. Quarterly report, September 1-November 30, 1980

    SciTech Connect

    1981-02-01

    Cell yield data for both Cu/sub 2/S/CdS and Cu/sub 2/S/(CdZn)S are reported. The presence of cracking in the n-type films is reported and the influence of composition and substrate material described. Design efforts for an analytical device that is basically a CdS cell on a transparent substrate, and a low cost gridding procedure are reported. A laser scanning system has been developed to detect incipient shorts and shunting in ungridded cells.

  4. Geothermal hydrogen sulfide removal

    SciTech Connect

    Urban, P.

    1981-04-01

    UOP Sulfox technology successfully removed 500 ppM hydrogen sulfide from simulated mixed phase geothermal waters. The Sulfox process involves air oxidation of hydrogen sulfide using a fixed catalyst bed. The catalyst activity remained stable throughout the life of the program. The product stream composition was selected by controlling pH; low pH favored elemental sulfur, while high pH favored water soluble sulfate and thiosulfate. Operation with liquid water present assured full catalytic activity. Dissolved salts reduced catalyst activity somewhat. Application of Sulfox technology to geothermal waters resulted in a straightforward process. There were no requirements for auxiliary processes such as a chemical plant. Application of the process to various types of geothermal waters is discussed and plans for a field test pilot plant and a schedule for commercialization are outlined.

  5. Hydrogen sulfide intoxication.

    PubMed

    Guidotti, Tee L

    2015-01-01

    Hydrogen sulfide (H2S) is a hazard primarily in the oil and gas industry, agriculture, sewage and animal waste handling, construction (asphalt operations and disturbing marshy terrain), and other settings where organic material decomposes under reducing conditions, and in geothermal operations. It is an insoluble gas, heavier than air, with a very low odor threshold and high toxicity, driven by concentration more than duration of exposure. Toxicity presents in a unique, reliable, and characteristic toxidrome consisting, in ascending order of exposure, of mucosal irritation, especially of the eye ("gas eye"), olfactory paralysis (not to be confused with olfactory fatigue), sudden but reversible loss of consciousness ("knockdown"), pulmonary edema (with an unusually favorable prognosis), and death (probably with apnea contributing). The risk of chronic neurcognitive changes is controversial, with the best evidence at high exposure levels and after knockdowns, which are frequently accompanied by head injury or oxygen deprivation. Treatment cannot be initiated promptly in the prehospital phase, and currently rests primarily on supportive care, hyperbaric oxygen, and nitrite administration. The mechanism of action for sublethal neurotoxicity and knockdown is clearly not inhibition of cytochrome oxidase c, as generally assumed, although this may play a role in overwhelming exposures. High levels of endogenous sulfide are found in the brain, presumably relating to the function of hydrogen sulfide as a gaseous neurotransmitter and immunomodulator. Prevention requires control of exposure and rigorous training to stop doomed rescue attempts attempted without self-contained breathing apparatus, especially in confined spaces, and in sudden release in the oil and gas sector, which result in multiple avoidable deaths. PMID:26563786

  6. Mineral commodity profiles: Cadmium

    USGS Publications Warehouse

    Butterman, W.C.; Plachy, Jozef

    2004-01-01

    Overview -- Cadmium is a soft, low-melting-point metal that has many uses. It is similar in abundance to antimony and bismuth and is the 63d element in order of crustal abundance. Cadmium is associated in nature with zinc (and, less closely, with lead and copper) and is extracted mainly as a byproduct of the mining and processing of zinc. In 2000, it was refined in 27 countries, of which the 8 largest accounted for two-thirds of world production. The United States was the third largest refiner after Japan and China. World production in 2000 was 19,700 metric tons (t) and U.S. production was 1,890 t. In the United States, one company in Illinois and another in Tennessee refined primary cadmium. A Pennsylvania company recovered cadmium from scrap, mainly spent nickel-cadmium (NiCd) batteries. The supply of cadmium in the world and in the United States appears to be adequate to meet future industrial needs; the United States has about 23 percent of the world reserve base.

  7. Field method for sulfide determination

    SciTech Connect

    Wilson, B L; Schwarser, R R; Chukwuenye, C O

    1982-01-01

    A simple and rapid method was developed for determining the total sulfide concentration in water in the field. Direct measurements were made using a silver/sulfide ion selective electrode in conjunction with a double junction reference electrode connected to an Orion Model 407A/F Specific Ion Meter. The method also made use of a sulfide anti-oxidant buffer (SAOB II) which consists of ascorbic acid, sodium hydroxide, and disodium EDTA. Preweighed sodium sulfide crystals were sealed in air tight plastic volumetric flasks which were used in standardization process in the field. Field standards were prepared by adding SAOB II to the flask containing the sulfide crystals and diluting it to the mark with deionized deaerated water. Serial dilutions of the standards were used to prepare standards of lower concentrations. Concentrations as low as 6 ppB were obtained on lake samples with a reproducibility better than +- 10%.

  8. Effect of bioturbation on metal-sulfide oxidation in surficial freshwater sediments

    SciTech Connect

    Peterson, G.S.; Ankley, G.T.; Leonard, E.N.

    1996-12-01

    Recent studies have demonstrated the role of acid-volatile sulfide (AVS) in controlling the bioavailability of several cationic metals in anoxic sediments. However, metal-sulfide complexes can be relatively labile with respect to oxidation associated with factors such as seasonal changes in rates of oxidation/production of AVS. Another potentially important mechanism of AVS oxidation in surficial sediments is bioturbation. The authors used different densities of the burrowing oligochaete Lumbriculus variegatus in a series of laboratory experiments to evaluate the effect of bioturbation on oxidation of AVS and subsequent bioavailability of cadmium and zinc spiked into freshwater sediments. Metal bioavailability was determined directly by bioaccumulation in the test organisms and indirectly through analysis of interstitial (pore) water metal concentrations. In the studies, horizon-specific sediment analyses were conducted to assess spatial differences in AVS and pore-water metal concentrations specifically related to organism activity. Burrowing activity of the oligochaete significantly reduced AVS concentrations in surficial sediments in a density-dependent manner and resulted in elevated interstitial water concentrations of cadmium but not zinc. Concentrations of cadmium in pore water from deeper horizons were consistently lower than those in the surficial sediments. The bioaccumulation of cadmium, but not zinc, but the oligochaetes. Overall, the results indicate that bioturbation can enhance the bioavailability of some cationic metals in surficial sediments, via oxidation of AVS, and demonstrate the importance of analyzing surficial sediments when assessing bioavailability of metals in sediments.

  9. Cadmium transporters in the kidney and cadmium-induced nephrotoxicity.

    PubMed

    Yang, Hong; Shu, Yan

    2015-01-09

    Among the organs in which the environmental pollutant cadmium causes toxicity, the kidney has gained the most attention in recent years. Numerous studies have sought to unravel the exact pathways by which cadmium enters the renal epithelial cells and the mechanisms by which it causes toxicity in the kidney. The purpose of this review is to present the progress made on the mechanisms of cadmium transport in the kidney and the role of transporter proteins in cadmium-induced nephrotoxicity.

  10. Cadmium migration in aerospace nickel cadmium cells

    NASA Technical Reports Server (NTRS)

    Mcdermott, P. P.

    1976-01-01

    The effects of temperature, the nature of separator material, charge and discharge, carbonate contamination, and the mode of storage are studied with respect to the migration of active material from the negative toward the positive plate. A theoretical model is proposed which takes into account the solubility of cadmium in various concentrations of hydroxide and carbonate at different temperatures, the generation of the cadmiate ion, Cd(OH)3(-), during discharge, the migration of the cadmiate ion and particulate Cd(OH)2 due to electrophoretic effects and the movement of electrolyte in and out of the negative plate and, finally, the recrystallization of cadmiate ion in the separator as Cd(OH)2. Application of the theoretical model to observations of cadmium migration in cycled cells is also discussed.

  11. Mechanical Activation-Assisted Reductive Leaching of Cadmium from Zinc Neutral Leaching Residue Using Sulfur Dioxide

    NASA Astrophysics Data System (ADS)

    Zhang, Chun; Min, Xiaobo; Chai, Liyuan; Zhang, Jianqiang; Wang, Mi

    2015-12-01

    In this work, zinc neutral leaching residue was mechanically activated by ball-milling. The subsequent leaching behavior and kinetics of cadmium extraction in a mixed SO2-H2SO4 system were studied. Changes in the crystalline phase, lattice distortion, particle size and morphology, which were induced by mechanical activation, were also investigated. The activated samples showed different physicochemical characteristics, and cadmium extraction was found to be easier than for the un-activated samples. Under the same conditions, mechanical activation contributed to higher cadmium leaching. The cadmium extraction kinetics at 75-95°C was found to fit the shrinking core model. The raw neutral leaching residue, and the samples activated for 60 min and 120 min had a calculated activation energy of 65.02 kJ/mol, 59.45 kJ/mol and 53.46 kJ/mol, respectively. The leaching residue was characterized by ICP, XRD and SEM analysis. According to XRD analysis, the main phases in the residue were lead sulfate (PbSO4), zinc sulfide (ZnS) and cadmium sulfide (CdS).

  12. The social costs of solar energy: A study of photovoltaic energy systems

    NASA Astrophysics Data System (ADS)

    Neff, T. L.

    An extensive analysis of the social costs of photovoltaic energy systems shows that there are potentially significant hazards associated with the manufacture and use of such technologies as large-crystal silicon, cadmium sulfide, and gallium arsenide solar cell arrays. The categories of applications considered were (1) decentralized residential installations, (2) decentralized neighborhood, commercial or industrial installations, and (3) central station plants. Summary and conclusion statements are presented for occupational health, public health, environmental impacts, labor, materials and energy impacts, and implications for technological development. It is thought in overview that there are reasons for optimism about the ability of photovoltaics to improve the balance of social costs and benefits in the energy sector.

  13. Plausible Mechanisms of Cadmium Carcinogenesis

    EPA Science Inventory

    Cadmium is a transition metal and an ubiquitous environmental and industrial pollutant. Laboratory animal studies and epidemiological studies have shown that exposure to cadmium is associated with various organ toxicities and carcinogenic effects. Several national and internation...

  14. Solution processing of next-generation nanocrystal solar cells

    NASA Astrophysics Data System (ADS)

    van Embden, J.; Chesman, A. S. R.; Duffy, N. W.; Della Gaspera, E.; Jasieniak, J. J.

    2013-12-01

    Next-generation solar cells will be fabricated from low-cost and earth abundant elements, using processes that are amenable to printing on a variety of light-weight substrates. The utilization of compositionally and structurally controlled colloidal nanocrystals as building blocks for such devices fulfills these criteria. Our recent efforts in developing kesterite Cu2ZnSnS4 (CZTS) nanocrystals, one of the most promising materials to emerge in this area, enable the deposition of CZTS thin-films directly from a variety of solution-processed methods. Nanocrystalline thin films possess poor electronic properties, which precludes their use in solar cell devices. In order to overcome this, thermal treatment steps under an atmosphere of vaporous selenium are applied to induce large scale crystallite growth and the production of selenized CZTSSe films. This process results in a highly photoactive p-type layer. The n-type cadmium sulfide layer is also deposited from solution using chemical bath deposition. We will discuss each of these accomplishments in detail, highlighting the significant challenges that need to be overcome in order to fabricate working CZTSSe thin film solar cells.

  15. Polycrystalline thin-film cadmium telluride solar cells fabricated by electrodeposition. Annual subcontract report, 20 March 1992--19 March 1993

    SciTech Connect

    Trefny, J.U.; Furtak, T.E.; Wada, N.; Williamson, D.L.; Kim, D.

    1993-08-01

    This report describes progress during the first year of a 3-year program at Colorado School of Mines, based upon earlier studies performed by Ametek Corporation, to develop specific layers of the Ametek n-i-p structure as well as additional studies of several transparent conducting oxides. Thin films of ZnO and ZnO:Al were deposited under various conditions. For the n-layer of the Ametek structure, a dip-coating method was developed for the deposition of CdS films. The authors also present data on the characterization of these films by X-ray diffraction, Raman spectroscopy, scanning tunneling microscopy, small-angle X-ray scattering, and other techniques. They made progress in the electrodeposition of the CdTe i-layer of the Ametek structure. They developed appropriate electrochemical baths and are beginning to understand the role of the many experimental parameters that must be controlled to obtain high-quality films of this material. They explored the possibility of using an electrochemical process for fabricating the ZnTe p-layer. Some preliminary success was achieved, and this step will be pursued in the next phase. Finally, they fabricated a number of ``dot`` solar cells with the structure glass/SnO{sub 2}/CdS/CdTe/Au. Several cells with efficiencies in the range of 5%-6% were obtained, and they are confident, given recent progress, that cells with efficiencies in excess of 10% will be achieved in the near future.

  16. Volcanogenic Massive Sulfide Deposit Density

    USGS Publications Warehouse

    Mosier, Dan L.; Singer, Donald A.; Berger, Vladimir I.

    2007-01-01

    A mineral-deposit density model for volcanogenic massive sulfide deposits was constructed from 38 well-explored control areas from around the world. Control areas contain at least one exposed volcanogenic massive sulfide deposit. The control areas used in this study contain 150 kuroko, 14 Urals, and 25 Cyprus massive sulfide subtypes of volcanogenic massive sulfide deposits. For each control area, extent of permissive rock, number of exposed volcanogenic massive sulfide deposits, map scale, deposit age, and deposit density were determined. The frequency distribution of deposit densities in these 38 control areas provides probabilistic estimates of the number of deposits for tracts that are permissive for volcanogenic massive sulfide deposits-90 percent of the control areas have densities of 100 or more deposits per 100,000 square kilometers, 50 percent of the control areas have densities of 700 or more deposits per 100,000 square kilometers, and 10 percent of the control areas have densities of 3,700 or more deposits per 100,000 square kilometers. Both map scale and the size of the control area are shown to be predictors of deposit density. Probabilistic estimates of the number of volcanogenic massive sulfide deposits can be made by conditioning the estimates on sizes of permissive area. The model constructed for this study provides a powerful tool for estimating the number of undiscovered volcanogenic massive sulfide deposits when conducting resource assessments. The value of these deposit densities is due to the consistency of these models with the grade and tonnage and the descriptive models. Mineral-deposit density models combined with grade and tonnage models allow reasonable estimates of the number, size, and grades of volcanogenic massive sulfide deposits to be made.

  17. A novel method for improving cerussite sulfidization

    NASA Astrophysics Data System (ADS)

    Feng, Qi-cheng; Wen, Shu-ming; Zhao, Wen-juan; Cao, Qin-bo; Lü, Chao

    2016-06-01

    Evaluation of flotation behavior, solution measurements, and surface analyses were performed to investigate the effects of chloride ion addition on the sulfidization of cerussite in this study. Micro-flotation tests indicate that the addition of chloride ions prior to sulfidization can significantly increase the flotation recovery of cerussite, which is attributed to the formation of more lead sulfide species on the mineral surface. Solution measurement results suggest that the addition of chloride ions prior to sulfidization induces the transformation of more sulfide ions from pulp solution onto the mineral surface by the formation of more lead sulfide species. X-ray diffraction and energy-dispersive spectroscopy indicate that more lead sulfide species form on the mineral surface when chloride ions are added prior to sulfidization. These results demonstrate that the addition of chloride ions prior to sulfidization can significantly improve the sulfidization of cerussite, thereby enhancing the flotation performance.

  18. Prevention of sulfide oxidation in sulfide-rich waste rock

    NASA Astrophysics Data System (ADS)

    Nyström, Elsa; Alakangas, Lena

    2015-04-01

    The ability to reduce sulfide oxidation in waste rock after mine closure is a widely researched area, but to reduce and/or inhibit the oxidation during operation is less common. Sulfide-rich (ca 30 % sulfur) waste rock, partially oxidized, was leached during unsaturated laboratory condition. Trace elements such as As and Sb were relatively high in the waste rock while other sulfide-associated elements such as Cu, Pb and Zn were low compared to common sulfide-rich waste rock. Leaching of unsaturated waste rock lowered the pH, from around six down to two, resulting in continuously increasing element concentrations during the leaching period of 272 days. The concentrations of As (65 mg/L), Cu (6.9 mg/L), Sb (1.2 mg/L), Zn (149 mg/L) and S (43 g/L) were strongly elevated at the end of the leaching period. Different alkaline industrial residues such as slag, lime kiln dust and cement kiln dust were added as solid or as liquid to the waste rock in an attempt to inhibit sulfide oxidation through neo-formed phases on sulfide surfaces in order to decrease the mobility of metals and metalloids over longer time scale. This will result in a lower cost and efforts of measures after mine closure. Results from the experiments will be presented.

  19. A statistical approach for optimizing parameters for electrodeposition of indium (III) sulfide (In2S3) films, potential low-hazard buffer layers for photovoltaic applications

    NASA Astrophysics Data System (ADS)

    Mughal, Maqsood Ali

    Clean and environmentally friendly technologies are centralizing industry focus towards obtaining long term solutions to many large-scale problems such as energy demand, pollution, and environmental safety. Thin film solar cell (TFSC) technology has emerged as an impressive photovoltaic (PV) technology to create clean energy from fast production lines with capabilities to reduce material usage and energy required to manufacture large area panels, hence, lowering the costs. Today, cost ($/kWh) and toxicity are the primary challenges for all PV technologies. In that respect, electrodeposited indium sulfide (In2S3) films are proposed as an alternate to hazardous cadmium sulfide (CdS) films, commonly used as buffer layers in solar cells. This dissertation focuses upon the optimization of electrodeposition parameters to synthesize In2S3 films of PV quality. The work describe herein has the potential to reduce the hazardous impact of cadmium (Cd) upon the environment, while reducing the manufacturing cost of TFSCs through efficient utilization of materials. Optimization was performed through use of a statistical approach to study the effect of varying electrodeposition parameters upon the properties of the films. A robust design method referred-to as the "Taguchi Method" helped in engineering the properties of the films, and improved the PV characteristics including optical bandgap, absorption coefficient, stoichiometry, morphology, crystalline structure, thickness, etc. Current density (also a function of deposition voltage) had the most significant impact upon the stoichiometry and morphology of In2S3 films, whereas, deposition temperature and composition of the solution had the least significant impact. The dissertation discusses the film growth mechanism and provides understanding of the regions of low quality (for example, cracks) in films. In2S3 films were systematically and quantitatively investigated by varying electrodeposition parameters including bath

  20. Reduced hydrogen cadmium plating

    SciTech Connect

    Hoeller, T.; Ross, L. ); Varma, R. ); Agarwala, V.S. )

    1991-01-01

    This paper demonstrates the advantages of using a periodic reverse pulse plating method, incorporating a fast cathodic pulse which is separated from the subsequent anodic/cathodic pulses by a long rest period in producing silvery cadmium coatings on steel from aqueous fluoroborate electrolyte. Also, the deposition obtained by combination of pulse currents and turbulent electrolyte flow system (forced convection of electrolyte, Re {approximately} 20-25,000) result in a near hydrogen-free electrodeposition of fine- grained cadmium. This is confirmed by the determination of diffusible hydrogen by the electrochemical (Barnach Electrode) method.

  1. Apparatus for use in sulfide chemiluminescence detection

    DOEpatents

    Spurlin, S.R.; Yeung, E.S.

    1987-01-06

    A method is described for chemiluminescently determining a sulfide which is either hydrogen sulfide or methyl mercaptan by reacting the sulfide with chlorine dioxide at low pressure and under conditions which allow a longer reaction time in emission of a single photon for every two sulfide containing species, and thereafter, chemiluminescently detecting and determining the sulfide. The invention also relates not only to the detection method, but the novel chemical reaction and a specifically designed chemiluminescence detection cell for the reaction. 4 figs.

  2. Apparatus for use in sulfide chemiluminescence detection

    DOEpatents

    Spurlin, Stanford R.; Yeung, Edward S.

    1987-01-01

    A method of chemiluminescently determining a sulfide which is either hydrogen sulfide or methyl mercaptan by reacting the sulfide with chlorine dioxide at low pressure and under conditions which allow a longer reaction time in emission of a single photon for every two sulfide containing species, and thereafter, chemiluminescently detecting and determining the sulfide. The invention also relates not only to the detection method, but the novel chemical reaction and a specifically designed chemiluminescence detection cell for the reaction.

  3. Fabrication and applications of copper sulfide (CuS) nanostructures

    NASA Astrophysics Data System (ADS)

    Shamraiz, Umair; Hussain, Raja Azadar; Badshah, Amin

    2016-06-01

    This review article presents different fabrication procedures (under the headlines of solvothermal routes, aerosol methods, solution methods and thermolysis), and applications (photocatalytic degradation, ablation of cancer cells, electrode material in lithium ion batteries and in gas sensing, organic solar cells, field emission properties, super capacitor applications, photoelectrochemical performance of QDSCs, photocatalytic reduction of organic pollutants, electrochemical bio sensing, enhanced PEC characteristics of pre-annealed CuS film electrodes) of copper sulfide (Covellite).

  4. [Acute and chronic cadmium poisoning].

    PubMed

    Andujar, P; Bensefa-Colas, L; Descatha, A

    2010-02-01

    Cadmium is a metallic impurity in various minerals. The two main cadmium exposure sources in general population are food and tobacco smoking. Its industrial exploitation has grown in the early twentieth century. Cadmium is used in accumulators or alkaline batteries (80%) and in pigments for paints or plastics (10%), in electrolytic process by deposit or by cadmium plating on metals or to reduce melting points (welding rods...). Cadmium is a cumulative toxic substance whose half-time for elimination is about 20 to 40 years and it is mainly stored in the liver and kidneys. Inhalation of cadmium oxide fumes may cause inhalation fevers or chemical pneumonitis. Cadmium chronic poisoning causes mainly renal tubulopathy and could be the cause of osteomalacia and diffuse osteoporosis. Cadmium is classified as certain carcinogen agent for humans by International Agency for Research on Cancer (IARC). The most relevant biological index exposure is the urinary cadmium. According to literature, no chelating agent can be still used in human cadmium poisonings. In France, some diseases caused by occupational exposure to cadmium may be compensated.

  5. Platinum metals magmatic sulfide ores.

    PubMed

    Naldrett, A J; Duke, J M

    1980-06-27

    Platinum-group elements (PGE) are mined predominantly from deposits that have formed by the segregation of molten iron-nickel-copper sulfides from silicate magmas. The absolute concentrations of PGE in sulfides from different deposits vary over a range of five orders of magnitude, whereas those of other chalcophile elements vary by factors of only 2 to 100. However, the relative proportions of the different PGE in a given deposit are systematically related to the nature of the parent magma. The absolute and relative concentrations of PGE in magmatic sulfides are explained in terms of the degree of partial melting of mantle peridotite required to produce the parent magma and the processes of batch equilibration and fractional segregation of sulfides. The Republic of South Africa and the U.S.S.R. together possess more than 97 percent of the world PGE reserves, but significant undeveloped resources occur in North America. The Stillwater complex in Montana is perhaps the most important example.

  6. Sulfide-mediated dehydrative glycosylation.

    PubMed

    Nguyen, H M; Chen, Y; Duron, S G; Gin, D Y

    2001-09-12

    The development of a new method for glycosylation with 1-hydroxy glycosyl donors employing dialkyl sulfonium reagents is described. The process employs the reagent combination of a dialkyl sulfide and triflic anhydride to effect anomeric bond constructions. This controlled dehydrative coupling of various C(1)-hemiacetal glycosyl donors and nucleophilic acceptors proceeds by way of a sulfide-to-sulfoxide oxidation process in which triflic anhydride serves as the oxidant.

  7. Chemical Bonding in Sulfide Minerals

    SciTech Connect

    Vaughan, David J.; Rosso, Kevin M.

    2006-08-01

    An understanding of chemical bonding and electronic structure in sulfide minerals is central to any attempt at understanding their crystal structures, stabilities and physical properties. It is also an essential precursor to understanding reactivity through modeling surface structure at the molecular scale. In recent decades, there have been remarkable advances in first principles (ab initio) methods for the quantitative calculation of electronic structure. These advances have been made possible by the very rapid development of high performance computers. Several review volumes that chart the applications of these developments in mineralogy and geochemistry are available (Tossell and Vaughan, 1992; Cygan and Kubicki, 2001). An important feature of the sulfide minerals is the diversity of their electronic structures, as evidenced by their electrical and magnetic properties (see Pearce et al. 2006, this volume). Thus, sulfide minerals range from insulators through semiconductors to metals, and exhibit every type of magnetic behavior. This has presented problems for those attempting to develop bonding models for sulfides, and also led to certain misconceptions regarding the kinds of models that may be appropriate. In this chapter, chemical bonding and electronic structure models for sulfides are reviewed with emphasis on more recent developments. Although the fully ab initio quantitative methods are now capable of a remarkable degree of sophistication in terms of agreement with experiment and potential to interpret and predict behavior with varying conditions, both qualitative and more simplistic quantitative approaches will also be briefly discussed. This is because we believe that the insights which they provide are still helpful to those studying sulfide minerals. In addition to the application of electronic structure models and calculations to solid sulfides, work on sulfide mineral surfaces (Rosso and Vaughan 2006a,b) and solution complexes and clusters (Rickard

  8. Hydrogen Sulfide Oxidation by Myoglobin.

    PubMed

    Bostelaar, Trever; Vitvitsky, Victor; Kumutima, Jacques; Lewis, Brianne E; Yadav, Pramod K; Brunold, Thomas C; Filipovic, Milos; Lehnert, Nicolai; Stemmler, Timothy L; Banerjee, Ruma

    2016-07-13

    Enzymes in the sulfur network generate the signaling molecule, hydrogen sulfide (H2S), from the amino acids cysteine and homocysteine. Since it is toxic at elevated concentrations, cells are equipped to clear H2S. A canonical sulfide oxidation pathway operates in mitochondria, converting H2S to thiosulfate and sulfate. We have recently discovered the ability of ferric hemoglobin to oxidize sulfide to thiosulfate and iron-bound hydropolysulfides. In this study, we report that myoglobin exhibits a similar capacity for sulfide oxidation. We have trapped and characterized iron-bound sulfur intermediates using cryo-mass spectrometry and X-ray absorption spectroscopy. Further support for the postulated intermediates in the chemically challenging conversion of H2S to thiosulfate and iron-bound catenated sulfur products is provided by EPR and resonance Raman spectroscopy in addition to density functional theory computational results. We speculate that the unusual sensitivity of skeletal muscle cytochrome c oxidase to sulfide poisoning in ethylmalonic encephalopathy, resulting from the deficiency in a mitochondrial sulfide oxidation enzyme, might be due to the concentration of H2S by myoglobin in this tissue. PMID:27310035

  9. Cadmium plating replacements

    NASA Technical Reports Server (NTRS)

    Nelson, Mary J.; Groshart, Earl C.

    1995-01-01

    The Boeing Company has been searching for replacements to cadmium plate. Two alloy plating systems seem close to meeting the needs of a cadmium replacement. The two alloys, zinc-nickel and tin-zinc are from alloy plating baths; both baths are neutral pH. The alloys meet the requirements for salt fog corrosion resistance, and both alloys excel as a paint base. Currently, tests are being performed on standard fasteners to compare zinc-nickel and tin-zinc on threaded hardware where cadmium is heavily used. The Hydrogen embrittlement propensity of the zinc-nickel bath has been tested, and just beginning for the tin-zinc bath. Another area of interest is the electrical properties on aluminum for tin-zinc and will be discussed. The zinc-nickel alloy plating bath is in production in Boeing Commercial Airplane Group for non-critical low strength steels. The outlook is promising that these two coatings will help The Boeing Company significantly reduce its dependence on cadmium plating.

  10. Cadmium-induced osteomalacia.

    PubMed Central

    Blainey, J D; Adams, R G; Brewer, D B; Harvey, T C

    1980-01-01

    The detailed study of a battery plate maker, who had worked with cadmium for 36 years, showed that proteinuria, typical of renal tubular dysfunction, had been observed for 25 years and during the last 12 years of his life the patient had suffered increasing disability from gross bone disease. Several bone biopsies and detailed metabolic studies showed typical severe osteomalacia, which responded well initially to calcium and vitamin D treatment. Examination of the liver both in life and after death showed a gross excess of cadmium. This was also found in the kidneys after death. Previously unreported changes were present in the bones, especially the lumbar vertebrae which were probably more the result of gross bone deformity than cadmium deposition. The mechanism of development of the severe acquired Fanconi syndrome was thought to be a combination of dietary calcium and vitamin D deficiency and impaired calcium absorption from abnormal vitamin D synthesis, related to the cadmium deposition in the renal tubules, which also caused the defect in renal tubular reabsorption. Images PMID:7426480

  11. CADMIUM PHOSPHATE GLASS

    DOEpatents

    Carpenter, H.W.; Johnson, P.D.

    1963-04-01

    A method of preparing a cadmium phosphate glass that comprises providing a mixture of solid inorganic compounds of cadmuim and phosphate having vaporizable components and heating the resulting composition to a temperature of at least 850 un. Concent 85% C is presented. (AEC)

  12. A novel single-precursor nanoparticle growth technique for luminescent metal sulfides (cadmium sulfide, lead sulfide, zinc sulfide) with hydrophilic surface modification

    NASA Astrophysics Data System (ADS)

    Rama, Jason Eric

    In recent years luminescent semiconductor nanoparticles (quantum dots) have attracted considerable attention, mostly due to their size-dependent tunable spectroscopic properties. Currently, fluorescing particles are put to use as biological labels alongside, or even replacing, fluorescing molecular probes. They are characterized by very narrow and tunable (excitonic) emission bands and long-range stability even under illumination. In particular, the colloidal chemistry approach to luminescent nanoparticle fabrication has been favored due to its relative ease, and high size tunability. However, the development of highly monodisperse, size tunable, and highly stable aqueous colloidal suspension fabrication methodologies has to date been very limited. In this work, the synthesis of luminescent MS (M = Cd, Pb, Zn) nanoparticles was achieved through the development and implementation of three characteristically different reaction methodologies: a spontaneous precipitation reaction (the metal chloride method), a controlled precipitation reaction (the metal oxide method), and a novel controlled aqueous decomposition reaction (the metal ethyl xanthate method) in an alkylamine solvent of 4-dimethylaminopyridine (DMAP). Varying degrees of monodispersity were achieved for the various methods, as evidenced by the photoluminescence full-width at half-maximum (FWHM). Spectral widths range from 150 nm for spontaneous precipitation methods, to as small as 20 nm for each of the temperature-controlled nucleation and ripening methods. For each of the methods, attempts at size tunability through variation of precursor concentration, growth temperature and growth time were performed. This resulted in the demonstration of an ability to fabricate size-specified semiconducting nanoparticles in the sub-10 nm size range. A demonstration of aqueous-organic-aqueous phase transfer versatility of the metal ethyl xanthate-DMAP fabrication method advances the potential of this particular method for many applications, including biological, microelectronic, and optoelectronic use.

  13. Assessment of cadmium in aquatic sediment using dialysis samplers with ion-exchange-resin collection

    SciTech Connect

    Shi, B.; Allen, H.E.; Desnoyers, C.

    1998-05-01

    Simultaneously extracted metals (SEM) and acid volatile sulfide (AVS) show the potential for toxicity on the basis of their ratio. Accordingly, the authors spiked cadmium in a range for which Cd/AVS ratios were from 0.2 to 10 in the sediment with its weight about 8 kg in each batch. Dialysis samplers with a cation ion-exchange resin (Dowex 50W-X4) collection were used in a laboratory for the determination of free cadmium concentrations in pore water of the collected sediment. When equilibrium was reached among cadmium in pore water, sediment, and ion-exchange resin, cadmium exchanged onto resin phase was regenerated with 1 N hydrochloric acid (OPTIMA grade) and determined using an atomic absorption spectrophotometer (Zeeman 5000) with a graphite furnace accessory. Cadmium determined using the dialysis sampler is considered as free cadmium which is related to the metal bioavailability toward aquatic biota. The developed methodology provides a new technique for assessment of free metal in aquatic sediment systems.

  14. Fabrication and investigation of the optoelectrical properties of MoS2/CdS heterojunction solar cells

    NASA Astrophysics Data System (ADS)

    Gu, Weixia; Yang, Fan; Wu, Chen; Zhang, Yi; Shi, Miaoyuan; Ma, Xiying

    2014-12-01

    Molybdenum disulfide (MoS2)/cadmium sulfide (CdS) heterojunction solar cells were successfully synthesized via chemical bath deposition (CBD) and chemical vapor deposition (CVD). The as-grown CdS film on a fluorine tin oxide (FTO) substrate deposited by CBD is continuous and compact. The MoS2 film deposited by CVD is homogeneous and continuous, with a uniform color and a thickness of approximately 10 nm. The optical absorption range of the MoS2/CdS heterojunction covers the visible and near-infrared spectral regions of 350 to 800 nm, which is beneficial for the improvement of solar cell efficiency. Moreover, the MoS2/CdS solar cell exhibits good current-voltage ( I- V) characteristics and pronounced photovoltaic behavior, with an open-circuit voltage of 0.66 V and a short-circuit current density of 0.227 × 10-6 A/cm2, comparable to the results obtained from other MoS2-based solar cells. This research is critical to investigate more efficient and stable solar cells based on graphene-like materials in the future.

  15. Fabrication and investigation of the optoelectrical properties of MoS2/CdS heterojunction solar cells

    PubMed Central

    2014-01-01

    Molybdenum disulfide (MoS2)/cadmium sulfide (CdS) heterojunction solar cells were successfully synthesized via chemical bath deposition (CBD) and chemical vapor deposition (CVD). The as-grown CdS film on a fluorine tin oxide (FTO) substrate deposited by CBD is continuous and compact. The MoS2 film deposited by CVD is homogeneous and continuous, with a uniform color and a thickness of approximately 10 nm. The optical absorption range of the MoS2/CdS heterojunction covers the visible and near-infrared spectral regions of 350 to 800 nm, which is beneficial for the improvement of solar cell efficiency. Moreover, the MoS2/CdS solar cell exhibits good current-voltage (I-V) characteristics and pronounced photovoltaic behavior, with an open-circuit voltage of 0.66 V and a short-circuit current density of 0.227 × 10-6 A/cm2, comparable to the results obtained from other MoS2-based solar cells. This research is critical to investigate more efficient and stable solar cells based on graphene-like materials in the future. PMID:25593552

  16. Fabrication and investigation of the optoelectrical properties of MoS2/CdS heterojunction solar cells.

    PubMed

    Gu, Weixia; Yang, Fan; Wu, Chen; Zhang, Yi; Shi, Miaoyuan; Ma, Xiying

    2014-01-01

    Molybdenum disulfide (MoS2)/cadmium sulfide (CdS) heterojunction solar cells were successfully synthesized via chemical bath deposition (CBD) and chemical vapor deposition (CVD). The as-grown CdS film on a fluorine tin oxide (FTO) substrate deposited by CBD is continuous and compact. The MoS2 film deposited by CVD is homogeneous and continuous, with a uniform color and a thickness of approximately 10 nm. The optical absorption range of the MoS2/CdS heterojunction covers the visible and near-infrared spectral regions of 350 to 800 nm, which is beneficial for the improvement of solar cell efficiency. Moreover, the MoS2/CdS solar cell exhibits good current-voltage (I-V) characteristics and pronounced photovoltaic behavior, with an open-circuit voltage of 0.66 V and a short-circuit current density of 0.227 × 10(-6) A/cm(2), comparable to the results obtained from other MoS2-based solar cells. This research is critical to investigate more efficient and stable solar cells based on graphene-like materials in the future.

  17. Chelating agents and cadmium intoxication

    SciTech Connect

    Shinobu, L.A.

    1985-01-01

    A wide range of conventional chelating agents have been screened for (a) antidotal activity in acute cadmium poisoning and (b) ability to reduce aged liver and kidney deposits of cadmium. Chelating agents belonging to the dithiocarbamate class have been synthesized and tested in both the acute and chronic modes of cadmium intoxication. Several dithiocarbamates, not only provide antidotal rescue, but also substantially decrease the intracellular deposits of cadmium associated with chronic cadmium intoxication. Fractionating the cytosol from the livers and kidneys of control and treated animals by Sephadex G-25 gel filtration clearly demonstrates that the dithiocarbamates are reducing the level of metallothionein-bound cadmium. However, the results of cell culture (Ehrlich ascites) studies designed to investigate the removal of cadmium from metallothionein and subsequent transport of the resultant cadmium complex across the cell membrane were inconclusive. In other in vitro investigations, the interaction between isolated native Cd, Zn-metallothionein and several chelating agents was explored. Ultracentrifugation, equilibrium dialysis, and Sephadex G-25 gel filtration studies have been carried out in an attempt to determine the rate of removal of cadmium from metallothionein by these small molecules. Chemical shifts for the relevant cadmium-dithiocarbamate complexes have been determined using natural abundance Cd-NMR.

  18. Reactivity of Sulfide Mineral Surfaces

    SciTech Connect

    Rosso, Kevin M.; Vaughan, David J.

    2006-08-01

    In the preceding chapter, the fundamental nature of sulfide mineral surfaces has been discussed, and the understanding we have of the ways in which the surface differs from a simple truncation of the bulk crystal structure reviewed. This naturally leads on to considering our understanding of sulfide surface chemistry, in the sense of how sulfide surfaces interact and react, particularly with gases and liquids. As noted elsewhere in this volume, research on sulfide mineral surfaces and surface reactivity is a relatively recent concern of mineralogists and geochemists, partly prompted by the availability of new imaging and spectroscopic methods, powerful computers and new computer algorithms. There has been a significantly longer history of sulfide mineral surface research associated with technologists working with, or within, the mining industry. Here, electrochemical methods, sometimes combined with analytical and spectroscopic techniques, have been used to probe surface chemistry. The motivation for this work has been to gain a better understanding of the controls of leaching reactions used to dissolve out metals from ores, or to understand the chemistry of the froth flotation systems used in concentrating the valuable (usually sulfide) minerals prior to metal extraction. The need for improved metal extraction technologies is still a major motivation for research on sulfide surfaces, but in the last couple of decades, new concerns have become important drivers for such work. In particular, much greater awareness of the negative environmental impact of acid and toxic metal-bearing waters derived from breakdown of sulfide minerals at former mining operations has prompted research on oxidation reactions, and on sorption of metals at sulfide surfaces. At the interface between fundamental geochemistry and industrial chemistry, the role of sulfide substrates in catalysis, and in the self-assembly and functionalization of organic molecules, has become an area of

  19. Sulfur and sulfides in chondrules

    NASA Astrophysics Data System (ADS)

    Marrocchi, Yves; Libourel, Guy

    2013-10-01

    The nature and distribution of sulfides within type I PO, POP and PP chondrules of the carbonaceous chondrite Vigarano (CV3) have been studied by secondary electron microscopy and electron microprobe. They occur predominantly as spheroidal blebs composed entirely of low-Ni iron sulfide (troilite, FeS) or troilite + magnetite but in less abundance in association with metallic Fe-Ni beads in opaque assemblages. Troilites are mainly located within the low-Ca pyroxene outer zone and their amounts increase with the abundance of low-Ca pyroxene within chondrules, suggesting co-crystallization of troilite and low-Ca pyroxene during high-temperature events. We show that sulfur concentration and sulfide occurrence in chondrules obey high temperature sulfur solubility and saturation laws. Depending on the fS2 and fO2 of the surrounding gas and on the melt composition, mainly the FeO content, sulfur dissolved in chondrule melts may eventually reach a concentration limit, the sulfur content at sulfide saturation (SCSS), at which an immiscible iron sulfide liquid separates from the silicate melt. The occurrence of both a silicate melt and an immiscible iron sulfide liquid is further supported by the non-wetting behavior of sulfides on silicate phases in chondrules due to the high interfacial tension between their precursor iron-sulfide liquid droplets and the surrounding silicate melt during the high temperature chondrule-forming event. The evolution of chondrule melts from PO to PP towards more silicic compositions, very likely due to high PSiO(g) of the surrounding nebular gas, induces saturation of FeS at much lower S content in PP than in PO chondrules, leading to the co-crystallization of iron sulfides and low-Ca pyroxenes. Conditions of co-saturation of low-Ca pyroxene and FeS are only achieved in non canonical environments characterized by high partial pressures of sulfur and SiO and redox conditions more oxidizing than IW-3. Fe and S mass balance calculations also

  20. Non-hydrolytic Sol-gel Synthesis of Tin Sulfides

    NASA Astrophysics Data System (ADS)

    Kaur, Rajvinder

    The non-hydrolytic sol-gel (NHSG) process is an effective low temperature route well known for preparing homogeneous metal oxides. Thermodynamically as well as kinetically favored products, which cannot be prepared with the traditional solid-state routes, can be produced using NHSG. This project is focused on the exploration of NHSG synthesis of binary tin sulfides. In the past few years, metal sulfides have been the subject of significant interest. Much effort has been devoted to understand these materials because of their potential applications in electronic, optical, and superconductor devices.4 Among these materials, tin sulfides are materials of technological importance, which are being explored as semiconductors, anode materials for Li ion batteries, photoconductors, photocatalysts and absorber layer materials in photovoltaic solar cell devices. All of these applications depend upon features like homogeneity, oxidation state, high surface area and purity of the materials. These properties can be difficult to achieve by employing traditional synthetic routes, which require high temperatures due to slow diffusion, limiting the products to thermodynamically stable phases and prohibiting control over properties like particle size and surface area. A variety of low temperature methods are being explored due to the increased demand for such advanced materials. This project is focused on exploring the NHSG approach to synthesize binary tin sulfides, with the main goal of establishing conditions for the targeted synthesis of different tin sulfide polymorphs with controlled particle size. Being non-oxide materials, tin sulfides can be air sensitive, which requires special attention in handling. All reactions were carried out in absence of oxygen. This project explores the reaction of tin halides with thioethers in a dry solvent medium, leading to the formation of tin sulfides. There are a number of synthetic parameters that can be varied for the NHSG approach. A

  1. Chemically Deposited Thin-Film Solar Cell Materials

    NASA Technical Reports Server (NTRS)

    Raffaelle, R.; Junek, W.; Gorse, J.; Thompson, T.; Harris, J.; Hehemann, D.; Hepp, A.; Rybicki, G.

    2005-01-01

    We have been working on the development of thin film photovoltaic solar cell materials that can be produced entirely by wet chemical methods on low-cost flexible substrates. P-type copper indium diselenide (CIS) absorber layers have been deposited via electrochemical deposition. Similar techniques have also allowed us to incorporate both Ga and S into the CIS structure, in order to increase its optical bandgap. The ability to deposit similar absorber layers with a variety of bandgaps is essential to our efforts to develop a multi-junction thin-film solar cell. Chemical bath deposition methods were used to deposit a cadmium sulfide (CdS) buffer layers on our CIS-based absorber layers. Window contacts were made to these CdS/CIS junctions by the electrodeposition of zinc oxide (ZnO). Structural and elemental determinations of the individual ZnO, CdS and CIS-based films via transmission spectroscopy, x-ray diffraction, x-ray photoelectron spectroscopy and energy dispersive spectroscopy will be presented. The electrical characterization of the resulting devices will be discussed.

  2. Cadmium biosorption by Saccharomyces cerevisiae

    SciTech Connect

    Volesky, B.; May, H.; Holan, Z.R. )

    1993-04-01

    Cadmium uptake by nonliving and resting cells of Saccharomyces cerevisiae obtained from aerobic or anaerobic cultures from pure cadmium-bearing solutions was examined. The highest cadmium uptake exceeding 70 mg Cd/g was observed with aerobic baker's yeast biomass from the exponential growth phase. Nearly linear sorption isotherms featured by higher sorbing resting cells together with metal deposits localized exclusively in vacuoles indicate the possibility of a different metal-sequestering mechanism when compared to dry nonliving yeasts which did not usually accumulate more than 20 mg Cd/g. The uptake of cadmium was relatively fast, 75% of the sorption completed in less than 5 min.

  3. Sulfide Stability of Planetary Basalts

    NASA Technical Reports Server (NTRS)

    Caiazza, C. M.; Righter, K.; Gibson, E. K., Jr.; Chesley, J. T.; Ruiz, J.

    2004-01-01

    The isotopic system, 187Re 187Os, can be used to determine the role of crust and mantle in magma genesis. In order to apply the system to natural samples, we must understand variations in Re/Os concentrations. It is thought that low [Os] and [Re] in basalts can be attributed to sulfide (FeS) saturation, as Re behaves incompatibly to high degrees of evolution until sulfide saturation occurs [1]. Previous work has shown that lunar basalts are sulfide under-saturated, and mid-ocean ridge, ocean-island and Martian (shergottites) basalts are saturated [2,3]. However, little is known about arc basalts. In this study, basaltic rocks were analyzed across the Trans-Mexican Volcanic Belt.

  4. A Reaction Involving Oxygen and Metal Sulfides.

    ERIC Educational Resources Information Center

    Hill, William D. Jr.

    1986-01-01

    Describes a procedure for oxygen generation by thermal decomposition of potassium chlorate in presence of manganese dioxide, reacted with various sulfides. Provides a table of sample product yields for various sulfides. (JM)

  5. Nickel sulfide hollow whisker formation

    SciTech Connect

    Holcomb, G.R.; Cramer, S.D.

    1997-02-01

    Hollow, high-aspect-ratio nickel sulfide whiskers were formed during aqueous corrosion experiments at 250 C by the US Department of Energy. The whiskers grew radially from Teflon thread at the waterline in acidic sodium sulfate solutions containing chloride additions. The hollow morphology is consistent with that reported for the mineral millerite found in nature in hematite cavities. The data suggest that iron and chloride impurities are necessary for the observed whisker structure. Hollow nickel sulfide whiskers were observed only in high-temperature corrosion experiments conducted on stainless steels; they were not observed in similar experiments on nickel-base alloys.

  6. 30 CFR 250.604 - Hydrogen sulfide.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 30 Mineral Resources 2 2010-07-01 2010-07-01 false Hydrogen sulfide. 250.604 Section 250.604... OPERATIONS IN THE OUTER CONTINENTAL SHELF Oil and Gas Well-Workover Operations § 250.604 Hydrogen sulfide. When a well-workover operation is conducted in zones known to contain hydrogen sulfide (H2S) or...

  7. 30 CFR 250.504 - Hydrogen sulfide.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 30 Mineral Resources 2 2010-07-01 2010-07-01 false Hydrogen sulfide. 250.504 Section 250.504... OPERATIONS IN THE OUTER CONTINENTAL SHELF Oil and Gas Well-Completion Operations § 250.504 Hydrogen sulfide. When a well-completion operation is conducted in zones known to contain hydrogen sulfide (H2S) or...

  8. 30 CFR 250.808 - Hydrogen sulfide.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 30 Mineral Resources 2 2010-07-01 2010-07-01 false Hydrogen sulfide. 250.808 Section 250.808... OPERATIONS IN THE OUTER CONTINENTAL SHELF Oil and Gas Production Safety Systems § 250.808 Hydrogen sulfide. Production operations in zones known to contain hydrogen sulfide (H2S) or in zones where the presence of...

  9. Nanostructured metal sulfides for energy storage.

    PubMed

    Rui, Xianhong; Tan, Huiteng; Yan, Qingyu

    2014-09-01

    Advanced electrodes with a high energy density at high power are urgently needed for high-performance energy storage devices, including lithium-ion batteries (LIBs) and supercapacitors (SCs), to fulfil the requirements of future electrochemical power sources for applications such as in hybrid electric/plug-in-hybrid (HEV/PHEV) vehicles. Metal sulfides with unique physical and chemical properties, as well as high specific capacity/capacitance, which are typically multiple times higher than that of the carbon/graphite-based materials, are currently studied as promising electrode materials. However, the implementation of these sulfide electrodes in practical applications is hindered by their inferior rate performance and cycling stability. Nanostructures offering the advantages of high surface-to-volume ratios, favourable transport properties, and high freedom for the volume change upon ion insertion/extraction and other reactions, present an opportunity to build next-generation LIBs and SCs. Thus, the development of novel concepts in material research to achieve new nanostructures paves the way for improved electrochemical performance. Herein, we summarize recent advances in nanostructured metal sulfides, such as iron sulfides, copper sulfides, cobalt sulfides, nickel sulfides, manganese sulfides, molybdenum sulfides, tin sulfides, with zero-, one-, two-, and three-dimensional morphologies for LIB and SC applications. In addition, the recently emerged concept of incorporating conductive matrices, especially graphene, with metal sulfide nanomaterials will also be highlighted. Finally, some remarks are made on the challenges and perspectives for the future development of metal sulfide-based LIB and SC devices. PMID:25073046

  10. Nanostructured metal sulfides for energy storage.

    PubMed

    Rui, Xianhong; Tan, Huiteng; Yan, Qingyu

    2014-09-01

    Advanced electrodes with a high energy density at high power are urgently needed for high-performance energy storage devices, including lithium-ion batteries (LIBs) and supercapacitors (SCs), to fulfil the requirements of future electrochemical power sources for applications such as in hybrid electric/plug-in-hybrid (HEV/PHEV) vehicles. Metal sulfides with unique physical and chemical properties, as well as high specific capacity/capacitance, which are typically multiple times higher than that of the carbon/graphite-based materials, are currently studied as promising electrode materials. However, the implementation of these sulfide electrodes in practical applications is hindered by their inferior rate performance and cycling stability. Nanostructures offering the advantages of high surface-to-volume ratios, favourable transport properties, and high freedom for the volume change upon ion insertion/extraction and other reactions, present an opportunity to build next-generation LIBs and SCs. Thus, the development of novel concepts in material research to achieve new nanostructures paves the way for improved electrochemical performance. Herein, we summarize recent advances in nanostructured metal sulfides, such as iron sulfides, copper sulfides, cobalt sulfides, nickel sulfides, manganese sulfides, molybdenum sulfides, tin sulfides, with zero-, one-, two-, and three-dimensional morphologies for LIB and SC applications. In addition, the recently emerged concept of incorporating conductive matrices, especially graphene, with metal sulfide nanomaterials will also be highlighted. Finally, some remarks are made on the challenges and perspectives for the future development of metal sulfide-based LIB and SC devices.

  11. 30 CFR 250.808 - Hydrogen sulfide.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 30 Mineral Resources 2 2012-07-01 2012-07-01 false Hydrogen sulfide. 250.808 Section 250.808 Mineral Resources BUREAU OF SAFETY AND ENVIRONMENTAL ENFORCEMENT, DEPARTMENT OF THE INTERIOR OFFSHORE OIL... § 250.808 Hydrogen sulfide. Production operations in zones known to contain hydrogen sulfide (H2S) or...

  12. 30 CFR 250.604 - Hydrogen sulfide.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 30 Mineral Resources 2 2011-07-01 2011-07-01 false Hydrogen sulfide. 250.604 Section 250.604...-Workover Operations § 250.604 Hydrogen sulfide. When a well-workover operation is conducted in zones known to contain hydrogen sulfide (H2S) or in zones where the presence of H2S is unknown (as defined...

  13. 30 CFR 250.504 - Hydrogen sulfide.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 30 Mineral Resources 2 2011-07-01 2011-07-01 false Hydrogen sulfide. 250.504 Section 250.504...-Completion Operations § 250.504 Hydrogen sulfide. When a well-completion operation is conducted in zones known to contain hydrogen sulfide (H2S) or in zones where the presence of H2S is unknown (as defined...

  14. 30 CFR 250.808 - Hydrogen sulfide.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 30 Mineral Resources 2 2014-07-01 2014-07-01 false Hydrogen sulfide. 250.808 Section 250.808 Mineral Resources BUREAU OF SAFETY AND ENVIRONMENTAL ENFORCEMENT, DEPARTMENT OF THE INTERIOR OFFSHORE OIL... § 250.808 Hydrogen sulfide. Production operations in zones known to contain hydrogen sulfide (H2S) or...

  15. 30 CFR 250.808 - Hydrogen sulfide.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 30 Mineral Resources 2 2013-07-01 2013-07-01 false Hydrogen sulfide. 250.808 Section 250.808 Mineral Resources BUREAU OF SAFETY AND ENVIRONMENTAL ENFORCEMENT, DEPARTMENT OF THE INTERIOR OFFSHORE OIL... § 250.808 Hydrogen sulfide. Production operations in zones known to contain hydrogen sulfide (H2S) or...

  16. Nanostructured metal sulfides for energy storage

    NASA Astrophysics Data System (ADS)

    Rui, Xianhong; Tan, Huiteng; Yan, Qingyu

    2014-08-01

    Advanced electrodes with a high energy density at high power are urgently needed for high-performance energy storage devices, including lithium-ion batteries (LIBs) and supercapacitors (SCs), to fulfil the requirements of future electrochemical power sources for applications such as in hybrid electric/plug-in-hybrid (HEV/PHEV) vehicles. Metal sulfides with unique physical and chemical properties, as well as high specific capacity/capacitance, which are typically multiple times higher than that of the carbon/graphite-based materials, are currently studied as promising electrode materials. However, the implementation of these sulfide electrodes in practical applications is hindered by their inferior rate performance and cycling stability. Nanostructures offering the advantages of high surface-to-volume ratios, favourable transport properties, and high freedom for the volume change upon ion insertion/extraction and other reactions, present an opportunity to build next-generation LIBs and SCs. Thus, the development of novel concepts in material research to achieve new nanostructures paves the way for improved electrochemical performance. Herein, we summarize recent advances in nanostructured metal sulfides, such as iron sulfides, copper sulfides, cobalt sulfides, nickel sulfides, manganese sulfides, molybdenum sulfides, tin sulfides, with zero-, one-, two-, and three-dimensional morphologies for LIB and SC applications. In addition, the recently emerged concept of incorporating conductive matrices, especially graphene, with metal sulfide nanomaterials will also be highlighted. Finally, some remarks are made on the challenges and perspectives for the future development of metal sulfide-based LIB and SC devices.

  17. Photovoltaic effect in individual asymmetrically contacted lead sulfide nanosheets.

    PubMed

    Dogan, Sedat; Bielewicz, Thomas; Lebedeva, Vera; Klinke, Christian

    2015-03-21

    Solution-processable, two-dimensional semiconductors are promising optoelectronic materials which could find application in low-cost solar cells. Lead sulfide nanocrystals raised attention since the effective band gap can be adapted over a wide range by electronic confinement and observed multi-exciton generation promises higher efficiencies. We report on the influence of the contact metal work function on the properties of transistors based on individual two-dimensional lead sulfide nanosheets. Using palladium we observed mobilities of up to 31 cm(2) V(-1) s(-1). Furthermore, we demonstrate that asymmetrically contacted nanosheets show photovoltaic effect and that the nanosheets' height has a decisive impact on the device performance. Nanosheets with a thickness of 5.4 nm contacted with platinum and titanium show a power conversion efficiency of up to 0.94% (EQE 75.70%). The results underline the high hopes put on such materials.

  18. Improved performance of CdS/CdSe quantum dots sensitized solar cell by incorporation of ZnO nanoparticles/reduced graphene oxide nanocomposite as photoelectrode

    NASA Astrophysics Data System (ADS)

    Ghoreishi, F. S.; Ahmadi, V.; Samadpour, M.

    2014-12-01

    Here we present novel quantum dot sensitized solar cells (QDSSC) based on ZnO nanoparticles (NPs)/reduced graphene oxide (RGO) nanocomposite photoanodes for better light harvesting and energy conversion. Photoelectrodes are prepared by doctor blading ZnO NPs/GO nanocomposite paste on a fluorine doped tin oxide substrate which are then sintered at 450 °C to obtain ZnO NPs/RGO nanocomposites. The partial reduction of GO after thermal reduction, is studied by Fourier transform infrared and Raman spectroscopies. Cadmium sulfide (CdS) and cadmium selenide (CdSe) quantum dots are deposited on the films through successive ionic layer adsorption and reaction and chemical bath deposition methods, respectively. The unique properties of ZnO NPs/RGO photoanodes, lead to a significant enhancement in the photovoltaic properties of solar cells in comparison with bare ZnO photoanodes. Current-voltage characteristics of cells are studied and the best results are obtained from ZnO NPs-RGO/CdS/CdSe with photoelectric conversion efficiency of 2.20% which is almost two times higher than cells which are made by pure ZnO NPs as photoanode (1.28%). Electrochemical impedance measurements show that the enhancement can be attributed to the increase of electron transfer rate in the ZnO NPs/RGO nanocomposite photoanode which arises from the ultrahigh electron mobility in graphene (RGO) sheets.

  19. Performance and Loss Analyses of High-Efficiency Chemical Bath Deposition (CBD)-ZnS/Cu(In1-xGax)Se2 Thin-Film Solar Cells

    NASA Astrophysics Data System (ADS)

    Pudov, Alexei; Sites, James; Nakada, Tokio

    2002-06-01

    Chemically deposited ZnS has been investigated as a buffer layer alternative to cadmium sulfide (CdS) in polycrystalline thin-film Cu(In1-xGax)Se2 (CIGS) solar cells. Cells with efficiency of up to 18.1% based on chemical bath deposition (CBD)-ZnS{\\slash}CIGS heterostructures have been fabricated. This paper presents the performance and loss analyses of these cells based on the current-voltage (J-V) and spectral response curves, as well as comparisons with high efficiency CBD-CdS/CIGS and crystalline silicon counterparts. The CBD-ZnS/CIGS devices have effectively reached the efficiency of the current record CBD-CdS/CIGS cell. The effects of the superior current of the CBD-ZnS/CIGS cell and the superior junction quality of the CBD-CdS/CIGS cell on overall performance nearly cancel each other.

  20. Ecofriendly and Nonvacuum Electrostatic Spray-Assisted Vapor Deposition of Cu(In,Ga)(S,Se)2 Thin Film Solar Cells.

    PubMed

    Hossain, Md Anower; Wang, Mingqing; Choy, Kwang-Leong

    2015-10-14

    Chalcopyrite Cu(In,Ga)(S,Se)2 (CIGSSe) thin films have been deposited by a novel, nonvacuum, and cost-effective electrostatic spray-assisted vapor deposition (ESAVD) method. The generation of a fine aerosol of precursor solution, and their controlled deposition onto a molybdenum substrate, results in adherent, dense, and uniform Cu(In,Ga)S2 (CIGS) films. This is an essential tool to keep the interfacial area of thin film solar cells to a minimum value for efficient charge separation as it helps to achieve the desired surface smoothness uniformity for subsequent cadmium sulfide and window layer deposition. This nonvacuum aerosol based approach for making the CIGSSe film uses environmentally benign precursor solution, and it is cheaper for producing solar cells than that of the vacuum-based thin film solar technology. An optimized CIGSSe thin film solar cell with a device configuration of molybdenum-coated soda-lime glass substrate/CIGSSe/CdS/i-ZnO/AZO shows the photovoltaic (j-V) characteristics of Voc=0.518 V, jsc=28.79 mA cm(-2), fill factor=64.02%, and a promising power conversion efficiency of η=9.55% under simulated AM 1.5 100 mW cm(-2) illuminations, without the use of an antireflection layer. This demonstrates the potential of ESAVD deposition as a promising alternative approach for making thin film CIGSSe solar cells at a lower cost.

  1. Platinum metals magmatic sulfide ores.

    PubMed

    Naldrett, A J; Duke, J M

    1980-06-27

    Platinum-group elements (PGE) are mined predominantly from deposits that have formed by the segregation of molten iron-nickel-copper sulfides from silicate magmas. The absolute concentrations of PGE in sulfides from different deposits vary over a range of five orders of magnitude, whereas those of other chalcophile elements vary by factors of only 2 to 100. However, the relative proportions of the different PGE in a given deposit are systematically related to the nature of the parent magma. The absolute and relative concentrations of PGE in magmatic sulfides are explained in terms of the degree of partial melting of mantle peridotite required to produce the parent magma and the processes of batch equilibration and fractional segregation of sulfides. The Republic of South Africa and the U.S.S.R. together possess more than 97 percent of the world PGE reserves, but significant undeveloped resources occur in North America. The Stillwater complex in Montana is perhaps the most important example. PMID:17796685

  2. p-Chlorophenyl methyl sulfide

    Integrated Risk Information System (IRIS)

    p - Chlorophenyl methyl sulfide ; CASRN 123 - 09 - 1 Human health assessment information on a chemical substance is included in the IRIS database only after a comprehensive review of toxicity data , as outlined in the IRIS assessment development process . Sections I ( Health Hazard Assessments for N

  3. Transition metal sulfide loaded catalyst

    DOEpatents

    Maroni, V.A.; Iton, L.E.; Pasterczyk, J.W.; Winterer, M.; Krause, T.R.

    1994-04-26

    A zeolite-based catalyst is described for activation and conversion of methane. A zeolite support includes a transition metal (Mo, Cr or W) sulfide disposed within the micropores of the zeolite. The catalyst allows activation and conversion of methane to C[sub 2]+ hydrocarbons in a reducing atmosphere, thereby avoiding formation of oxides of carbon.

  4. Transition metal sulfide loaded catalyst

    DOEpatents

    Maroni, Victor A.; Iton, Lennox E.; Pasterczyk, James W.; Winterer, Markus; Krause, Theodore R.

    1994-01-01

    A zeolite based catalyst for activation and conversion of methane. A zeolite support includes a transition metal (Mo, Cr or W) sulfide disposed within the micropores of the zeolite. The catalyst allows activation and conversion of methane to C.sub.2 + hydrocarbons in a reducing atmosphere, thereby avoiding formation of oxides of carbon.

  5. Amorphous molybdenum sulfides as hydrogen evolution catalysts.

    PubMed

    Morales-Guio, Carlos G; Hu, Xile

    2014-08-19

    Providing energy for a population projected to reach 9 billion people within the middle of this century is one of the most pressing societal issues. Burning fossil fuels at a rate and scale that satisfy our near-term demand will irreversibly damage the living environment. Among the various sources of alternative and CO2-emission-free energies, the sun is the only source that is capable of providing enough energy for the whole world. Sunlight energy, however, is intermittent and requires an efficient storage mechanism. Sunlight-driven water splitting to make hydrogen is widely considered as one of the most attractive methods for solar energy storage. Water splitting needs a hydrogen evolution catalyst to accelerate the rate of hydrogen production and to lower the energy loss in this process. Precious metals such as Pt are superior catalysts, but they are too expensive and scarce for large-scale applications. In this Account, we summarize our recent research on the preparation, characterization, and application of amorphous molybdenum sulfide catalysts for the hydrogen evolution reaction. The catalysts can be synthesized by electrochemical deposition under ambient conditions from readily available and inexpensive precursors. The catalytic activity is among the highest for nonprecious catalysts. For example, at a loading of 0.2 mg/cm(2), the optimal catalyst delivers a current density of 10 mA/cm(2) at an overpotential of 160 mV. The growth mechanism of the electrochemically deposited film catalysts was revealed by an electrochemical quartz microcrystal balance study. While different electrochemical deposition methods produce films with different initial compositions, the active catalysts are the same and are identified as a "MoS(2+x)" species. The activity of the film catalysts can be further promoted by divalent Fe, Co, and Ni ions, and the origins of the promotional effects have been probed. Highly active amorphous molybdenum sulfide particles can also be prepared

  6. A field investigation of the relationship between zinc and acid volatile sulfide concentrations in freshwater sediments

    USGS Publications Warehouse

    Ankley, Gerald T.; Liber, Karsten; Call, Daniel J.; Markee, Thomas P.; Canfield, Timothy J.; Ingersoll, Christopher G.

    1996-01-01

    Understanding relationships between cationic metals such as cadmium, copper, nickel, lead and zinc, and amorphous iron sulfides, measured as acid volatile sulfide (AVS), is key to predicting metal bioavailability and toxicity insediments. The objective of the present study was to assess seasonal and spatial variations of AVS in freshwater sediments contaminated with zinc. Sediments were sampled from three streams with varying levels of zinc contamination at two different times, March and June of 1995, representing cold- and warm-weather situations. Interstitial (pore) water concentrations of zinc, and solid phase concentrations of AVS and zinc were measured in surficial and deep sediment horizons. Toxicity tests (10-d) with the amphipodHyalella azteca were conducted using intact cores. Sediment zinc concentrations from six sites within the primary test stream differed by about five-fold, and also varied seasonally. Acid volatile sulfide concentrations were generally lower than those of zinc, and pore water zinc concentrations typically were elevated. There was a positive correlation between solid-phase AVS and zinc concentrations, suggesting that the system was dominated by zinc, as opposed to iron sulfides. In contrast to expectations arising from some studies of seasonal variations of AVS in iron-dominated systems, AVS concentrations were smaller in June than in March. However, this was likely due to a major storm event and associated sediment scouring before the June sampling, rather than to seasonal processes related to variations in temperature and dissolved oxygen. Based upon an indirect analysis of depth variations in AVS, there was some indication that zinc sulfide might be less prone to oxidation than iron sulfide. There was a strong correlation between toxicity of the sediment samples toH. azteca and interstitial water concentrations of zinc; however, the possible contribution of other contaminants to sediment toxicity cannot be dismissed.

  7. Dissolved sulfides in the oxic water column of San Francisco Bay, California

    USGS Publications Warehouse

    Kuwabara, J.S.; Luther, G.W.

    1993-01-01

    Trace contaminants enter major estuaries such as San Francisco Bay from a variety of point and nonpoint sources and may then be repartitioned between solid and aqueous phases or altered in chemical speciation. Chemical speciation affects the bioavailability of metals as well as organic ligands to planktonic and benthic organisms, and the partitioning of these solutes between phases. Our previous, work in south San Francisco Bay indicated that sulfide complexation with metals may be of particular importance because of the thermodynamic stability of these complexes. Although the water column of the bay is consistently well-oxygenated and typically unstratified with respect to dissolved oxygen, the kinetics of sulfide oxidation could exert at least transient controls on metal speciation. Our initial data on dissolved sulfides in the main channel of both the northern and southern components of the bay consistently indicate submicromolar concenrations (from <1 nM to 162 nM), as one would expect in an oxidizing environment. However, chemical speciation calculations over the range of observed sulfide concentrations indicate that these trace concentrations in the bay water column can markedly affect chemical speciation of ecologically significant trace metals such as cadmium, copper, and zinc.

  8. The photoluminescence and phase composition of lead sulphide–cadmium sulphide layers obtained by chemical bath deposition

    NASA Astrophysics Data System (ADS)

    Maraeva, E. V.; Shupta, A. A.; Bobkov, A. A.; Levitskii, V. S.; Maximov, A. I.; Moshnikov, V. A.

    2016-08-01

    The study concerns optical properties and phase composition studies of the layers based on cadmium sulfide–lead sulfide synthesized by the hydro-chemical deposition. The presence of two peaks in the photoluminescence spectra presumably correspond to two different CdS modifications, i.e. the cubic structure of zinc blende and hexagonal structure (wurtzite type). X-ray phase analysis (XRPA) confirmes the presence of both types of crystallites.

  9. Sulfur transformations at the hydrogen sulfide/oxygen interface in stratified waters and in cyanobacterial mats

    NASA Technical Reports Server (NTRS)

    Cohen, Y.

    1985-01-01

    Stratified water bodies allow the development of several microbial plates along the water column. The microbial plates develop in relation to nutrient availability, light penetration, and the distribution of oxygen and sulfide. Sulfide is initially produced in the sediment by sulfate-reducing bacteria. It diffuses along the water column creating a zone of hydrogen sulfide/oxygen interface. In the chemocline of Solar Lake oxygen and sulfide coexist in a 0 to 10 cm layer that moves up and down during a diurnal cycle. The microbial plate at the chemocline is exposed to oxygen and hydrogen sulfide, alternating on a diurnal basis. The cyanobacteria occupying the interface switch from anoxygenic photosynthesis in the morning to oxygenic photosynthesis during the rest of the day which results in a temporal build up of elemental sulfur during the day and disappears at night due to both oxidation to thiosulfate and sulfate by thiobacilli, and reduction to hydrogen sulfide by Desulfuromonas sp. and anaerobically respiring cyanobacteria. Sulfate reduction was enhanced in the light at the surface of the cyanobacterial mats. Microsulfate reduction measurements showed enhanced activity of sulfate reduction even under high oxygen concentrations of 300 to 800 micrometer. Apparent aerobic SO sub 4 reduction activity is explained by the co-occurrence of H sub 2. The physiology of this apparent sulfate reduction activity is studied.

  10. Marine diagenesis of hydrothermal sulfide

    SciTech Connect

    Moammar, M.O.

    1985-01-01

    An attempt is made to discuss the artificial and natural oxidation and hydrolysis of hydrothermal sulfide upon interaction with normal seawater. Synthetic and natural ferrosphalerite particles used in kinetic oxidation and hydrolysis studies in seawater develop dense, crystalline coatings consisting of ordered and ferrimagnetic delta-(Fe, Zn)OOH. Due to the formation of this reactive diffusion barrier, the release of Zn into solution decreases rapidly, and sulfide oxidation is reduced to a low rate determined by the diffusion of oxygen through the oxyhydroxide film. This also acts as an efficient solvent for ions such as Zn/sup 2 +/, Ca/sup 2 +/, and possibly Cd/sup 2 +/, which contribute to the stabilization of the delta-FeOOH structure. The oxidation of sulfide occurs in many seafloor spreading areas, such as 21/sup 0/N on the East Pacific Ridge. In these areas the old surface of the sulfide chimneys are found to be covered by an orange stain, and sediment near the base of nonactive vents is also found to consist of what has been referred to as amorphous iron oxide and hydroxide. This thesis also discusses the exceedingly low solubility of zinc in seawater, from delta-(Fe, Zn)OOH and the analogous phase (zinc-ferrihydroxide) and the zinc exchange minerals, 10-A manganate and montmorillonite. The concentrations of all four are of the same magnitude (16, 36.4, and 12 nM, respectively) as the zinc concentration in deep ocean water (approx. 10 nM), which suggests that manganates and montmorillonite with iron oxyhydroxides control zinc concentration in the deep ocean.

  11. Sulfide smelting using Ausmelt technology

    NASA Astrophysics Data System (ADS)

    Mounsey, Edward N.; Robilliard, Ken R.

    1994-08-01

    Over the past decade, Ausmelt has been developing the top submerged lancing process for the smelting of sulfidic ores to recover such metals as copper, lead, silver, tin, antimony, and nickel as well as for separation of minor elements such as arsenic, antimony, and bismuth. Development has taken place in Ausmelt's pilot plant in Dandenong, near Melbourne, Australia. A number of projects have proceeded to commercial-scale operation. This paper reviews developments at both the pilot and commercial scales.

  12. Metal sulfide for battery applications

    SciTech Connect

    Guidotti, R.A.

    1988-01-01

    A number of metal sulfides can be used in batteries as a cathode (reducible) material as part of an electrochemical couple to provide energy. There are a number of physical and chemical characteristics that can be evaluated for screening potential candidates for use in batteries. These include: cell potential vs. Li, thermal and chemical stability, electrical conductivity, allotropic form (phase), reaction kinetics during discharge, type of discharge mechanism, and material rechargeability. These are reviewed in general, with emphasis on sulfides of copper, iron, and molybdenum which are currently being used as cathodes in Li and Li-alloy batteries. The presence of impurities can adversely impact performance when naturally occurring sulfide minerals are used for battery applications. Sandia National Laboratories uses natural pyrite (FeS2) for its high-temperature, thermally activated Li(Si)/FeS2 batteries. The purification and processing procedures for the FeS2 involves both chemical and physical methods. Flotation was found to yield comparable results as HF leaching for removal of silica, but without the negative health and environmental concerns associated with this technique. 11 refs., 5 figs., 6 tabs.

  13. Chemical dissolution of sulfide minerals

    USGS Publications Warehouse

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

    1977-01-01

    Chemical dissolution treatments involving the use of aqua regia, 4 N HNO3, H2O2-ascorbic acid, oxalic acid, KClO3+HCl, and KClO3+HCl followed by 4 N HNO3 were applied to specimens of nine common sulfide minerals (galena, chalcopyrite, cinnabar, molybdenite, orpiment, pyrite, stibnite, sphalerite, and tetrahedrite) mixed individually with a clay loam soil. The resultant decrease in the total sulfur content of the mixture, as determined by using the Leco induction furnace, was used to evaluate the effectiveness of each chemical treatment. A combination of KClO3+HCl followed by 4 N HNO3 boiling gently for 20 min has been shown to be very effective in dissolving all the sulfide minerals. This treatment is recommended to dissolve metals residing in sulfide minerals admixed with secondary weathering products, as one step in a fractionation scheme whereby metals in soluble and adsorbed forms, and those associated with organic materials and secondary oxides, are first removed by other chemical extractants.

  14. Sulfide-Driven Microbial Electrosynthesis

    SciTech Connect

    Gong, YM; Ebrahim, A; Feist, AM; Embree, M; Zhang, T; Lovley, D; Zengler, K

    2013-01-01

    Microbial electrosynthesis, the conversion of carbon dioxide to organic molecules using electricity, has recently been demonstrated for acetogenic microorganisms, such as Sporomusa ovata. The energy for reduction of carbon dioxide originates from the hydrolysis of water on the anode, requiring a sufficiently low potential. Here we evaluate the use of sulfide as an electron source for microbial electrosynthesis. Abiotically oxidation of sulfide on the anode yields two electrons. The oxidation product, elemental sulfur, can be further oxidized to sulfate by Desulfobulbus propionicus, generating six additional electrons in the process. The eight electrons generated from the combined abiotic and biotic steps were used to reduce carbon dioxide to acetate on a graphite cathode by Sporomusa ovata at a rate of 24.8 mmol/day.m(2). Using a strain of Desulfuromonas as biocatalyst on the anode resulted in an acetate production rate of 49.9 mmol/day.m(2), with a Coulombic efficiency of over 90%. These results demonstrate that sulfide can serve effectively as an alternative electron donor for microbial electrosynthesis.

  15. Detoxification of mercury, cadmium, and lead in Klebsiella aerogenes NCTC 418 growing in continuous culture

    SciTech Connect

    Aiking, H.; Govers, H.; van 'T Riet, J.

    1985-11-01

    Klebsiella aerogenes NCTC 418 growing in the presence of cadmium under glucose-, sulfate-, or phosphate-limited conditions in continuous culture exhibited sulfide formation and P/sub i/ accumulation as the only demonstrable detoxification mechanisms. In the presence of mercury under similar conditions only HgS formation could be confirmed, by an increased sensitivity to mercury under sulfate-limited conditions, among others. The fact that the cells were most sensitive to cadmium under conditions of phosphate limitation and most sensitive to mercury under conditions of sulfate limitation led to the hypothesis that these inorganic detoxification mechanisms generally depended on a kind of facilitated precipitation. The process was coined thus because heavy metals were probably accumulated and precipitated near the cell perimeter due to the relatively high local concentrations of sulfide and phosphate there. Depending on the growth-limiting nutrient, mercury proved to be 25-fold (phosphate limitation), 75-fold (glycerol limitation), or 150-fold (sulfate limitation) more toxic than cadmium to this organism. In the presence of lead, PbS formation was suggested. since no other detoxification mechanisms were detected, for example, rendering heavy metal ions innocuous as metallo-organic compounds, it was concluded that formation of heavy metal precipitates is crucially important to this organism. In addition, it was observed that several components of a defined mineral medium were able to reduce mercuric ions to elemental mercury. This abiotic mercury volatilization was studied in detail, and its general and environmental implications are discussed.

  16. Cadmium effects on the thyroid gland.

    PubMed

    Jancic, Snezana A; Stosic, Bojan Z

    2014-01-01

    Cadmium has been listed as one of the 126 priority pollutants and a category I carcinogen. Carcinogenic effects of cadmium on the lungs, testicles, and prostate are widely recognized, but there has been insufficient research on the effect of cadmium on the thyroid gland. Cadmium has the affinity to accumulate not only in the liver, kidneys, and pancreas but also in the thyroid gland. It has been established that cadmium blood concentration correlates positively with its accumulation in the thyroid gland. Women of fertile age have higher cadmium blood and urine concentrations than men. In spite of its redox inertia, cadmium brings about oxidative stress and damage to the tissue by indirect mechanisms. Mitochondria are considered to be the main intracellular targets for cadmium. Colloid cystic goiter, adenomatoid follicular hyperplasia with low-grade dysplasia and thyroglobulin hypo- and asecretion, and parafollicular cell diffuse and nodular hyperplasia and hypertrophy are often found in chronic cadmium toxicity. PMID:24388198

  17. Cadmium effects on the thyroid gland.

    PubMed

    Jancic, Snezana A; Stosic, Bojan Z

    2014-01-01

    Cadmium has been listed as one of the 126 priority pollutants and a category I carcinogen. Carcinogenic effects of cadmium on the lungs, testicles, and prostate are widely recognized, but there has been insufficient research on the effect of cadmium on the thyroid gland. Cadmium has the affinity to accumulate not only in the liver, kidneys, and pancreas but also in the thyroid gland. It has been established that cadmium blood concentration correlates positively with its accumulation in the thyroid gland. Women of fertile age have higher cadmium blood and urine concentrations than men. In spite of its redox inertia, cadmium brings about oxidative stress and damage to the tissue by indirect mechanisms. Mitochondria are considered to be the main intracellular targets for cadmium. Colloid cystic goiter, adenomatoid follicular hyperplasia with low-grade dysplasia and thyroglobulin hypo- and asecretion, and parafollicular cell diffuse and nodular hyperplasia and hypertrophy are often found in chronic cadmium toxicity.

  18. Cadmium telluride (CdTe) and cadmium selenide (CdSe) leaching behavior and surface chemistry in response to pH and O2.

    PubMed

    Zeng, Chao; Ramos-Ruiz, Adriana; Field, Jim A; Sierra-Alvarez, Reyes

    2015-05-01

    Cadmium telluride (CdTe) and cadmium selenide (CdSe) are increasingly being applied in photovoltaic solar cells and electronic components. A major concern is the public health and ecological risks associated with the potential release of toxic cadmium, tellurium, and/or selenium species. In this study, different tests were applied to investigate the leaching behavior of CdTe and CdSe in solutions simulating landfill leachate. CdTe showed a comparatively high leaching potential. In the Toxicity Characteristic Leaching Procedure (TCLP) and Waste Extraction Test (WET), the concentrations of cadmium released from CdTe were about 1500 and 260 times higher than the regulatory limit (1 mg/L). In contrast, CdSe was relatively stable and dissolved selenium in both leaching tests was below the regulatory limit (1 mg/L). Nonetheless, the regulatory limit for cadmium was exceeded by 5- to 6- fold in both tests. Experiments performed under different pH and redox conditions confirmed a marked enhancement in CdTe and CdSe dissolution both at acidic pH and under aerobic conditions. These findings are in agreement with thermodynamic predictions. Taken as a whole, the results indicate that recycling of decommissioned CdTe-containing devices is desirable to prevent the potential environmental release of toxic cadmium and tellurium in municipal landfills.

  19. Iron-Nickel Sulfide Compositional Ranges in CM Chondrites: No Simple Plan

    NASA Technical Reports Server (NTRS)

    Zolensky, Michael; Le, Loan

    2003-01-01

    Iron-nickel sulfides are found in most or all solar system environments, and are probably the only minerals found in all extraterrestrial materials on hand. Despite this ubiquity, they have only just begun the attention they deserve. The most common Fe-Ni sulfides in chondrites are troilite (FeS), pyrrhotite (Fe(1-x)S) and pentlandite (Fe,Ni)9S8. Troilite is believed to have resulted from sulfidation of metal (Fe-Ni) grains in an H2S-containing environment. Pyrrhotite is produced when friable troilite grains, which are exfoliated from the metal nucleus, are submitted to continued sulfidation. Some asteroids are known to have experienced aqueous alteration, forming products including new generations of sulfides (pyrrhotite and pentlandite). Pentlandite in particular is known to form during such alteration. However, experimental work by Lauretta has indicated that pentlandite may also have been formed during the initial sulfidation process, due to the faster diffusion rate of nickel into the forming sulfide, as compared to iron. Finally, there is considerable evidence for a family of phases intermediate between pyrrhotite and pentlandite, following the trend of the high temperature monosulfide solid solution, something not encountered in terrestrial rocks. Each sulfide has its own particular stability conditions, which have been determined for most phases. The long-term objective of our research is to characterize sulfides in chondritic materials in order to better establish the conditions under which they formed, and the subsequent processes they experienced. Ultimately, it will be possible to infer whether the sulfides in the chondrites were formed in the solar nebula or on asteroids, and if formed on the asteroids, deduce how much alteration has occurred there. Here we explore the relationships between the finest grain size portions of carbonaceous chondrites, these being matrix and chondrule rims; fine-grained materials are the most sensitive to their environment

  20. Stimulation of Cadmium Uptake in Relation to the Cadmium Content of Plants 1

    PubMed Central

    Petit, Charles M.; Ringoet, Arthur; Myttenaere, Constant

    1978-01-01

    The time course of cadmium uptake by the roots of intact tomato plants (Lycopersicon esculentum Mill.) was measured in a nutrient solution with a micromolar cadmium concentration until all cadmium in the medium was exhausted. Exhaustion taking a few hours, cadmium was repeatedly added to the nutrient solution. The initial rate of cadmium uptake was computed for each cadmium addition. This rate sharply increased and ultimately leveled off, the maximum value being about three times higher than the value measured after the first cadmium addition. The stimulating effect of cadmium was associated with an inhibitory effect at higher levels of cadmium concentrations. An increase in the net cadmium influx with time could not be explained by the binding of heavy metal to a fixed number of organic compounds. Conceivably, the production of binding sites could be increased and cadmium might play a part in controlling the rate of sites production. PMID:16660557

  1. Mercury Telluride and Cadmium Telluride

    NASA Technical Reports Server (NTRS)

    2004-01-01

    A semiconductor's usefulness is determined by how atoms are ordered within the crystal's underlying three-dimensional structure. While this mercury telluride and cadmium telluride alloy sample mixes completely in Earth -based laboratories, convective flows prevent them from mixing uniformly.

  2. 30 CFR 250.604 - Hydrogen sulfide.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 30 Mineral Resources 2 2014-07-01 2014-07-01 false Hydrogen sulfide. 250.604 Section 250.604... § 250.604 Hydrogen sulfide. When a well-workover operation is conducted in zones known to contain hydrogen sulfide (H2S) or in zones where the presence of H2S is unknown (as defined in § 250.490 of...

  3. 30 CFR 250.504 - Hydrogen sulfide.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 30 Mineral Resources 2 2014-07-01 2014-07-01 false Hydrogen sulfide. 250.504 Section 250.504... § 250.504 Hydrogen sulfide. When a well-completion operation is conducted in zones known to contain hydrogen sulfide (H2S) or in zones where the presence of H2S is unknown (as defined in § 250.490 of...

  4. 30 CFR 250.604 - Hydrogen sulfide.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 30 Mineral Resources 2 2013-07-01 2013-07-01 false Hydrogen sulfide. 250.604 Section 250.604... § 250.604 Hydrogen sulfide. When a well-workover operation is conducted in zones known to contain hydrogen sulfide (H2S) or in zones where the presence of H2S is unknown (as defined in § 250.490 of...

  5. 30 CFR 250.504 - Hydrogen sulfide.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 30 Mineral Resources 2 2012-07-01 2012-07-01 false Hydrogen sulfide. 250.504 Section 250.504... § 250.504 Hydrogen sulfide. When a well-completion operation is conducted in zones known to contain hydrogen sulfide (H2S) or in zones where the presence of H2S is unknown (as defined in § 250.490 of...

  6. 30 CFR 250.604 - Hydrogen sulfide.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 30 Mineral Resources 2 2012-07-01 2012-07-01 false Hydrogen sulfide. 250.604 Section 250.604... § 250.604 Hydrogen sulfide. When a well-workover operation is conducted in zones known to contain hydrogen sulfide (H2S) or in zones where the presence of H2S is unknown (as defined in § 250.490 of...

  7. 30 CFR 250.504 - Hydrogen sulfide.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 30 Mineral Resources 2 2013-07-01 2013-07-01 false Hydrogen sulfide. 250.504 Section 250.504... § 250.504 Hydrogen sulfide. When a well-completion operation is conducted in zones known to contain hydrogen sulfide (H2S) or in zones where the presence of H2S is unknown (as defined in § 250.490 of...

  8. Aversiveness of cadmium in solution.

    PubMed

    Cory-Slechta, D A; Weiss, B

    1981-12-01

    Weanling rats were given cadmium chloride solutions as drinking water (0, 25, 50 or 150 ppm Cd). Immediate decrements in fluid consumption and retarded weight gain were observed at the highest concentration. In addition, two of the 150 ppm rats died within four days. The rapid onset of these effects suggested taste aversion and sharply reduced water intake, not physiological impairment, as the cause. To test this possibility, rats were given a choice between two drinking water solutions. One contained distilled water, the other cadmium. Concentrations as low as 1 ppm were rejected by some rats. Additional studies showed that chronic cadmium exposure modified the intake pattern of saccharin solutions typical of rats, and that the addition of saccharin to the 150 ppm cadmium solution did not reduce its aversive properties. These data indicated that the taste of cadmium, at least in solution, is aversive to rats. Since taste aversion can reduce fluid and food consumption, and consequently body weight, properly designed experiments must include adequate control procedures such as pair-feeding and pair-watering to differentiate unique effects of cadmium from those produced by undernutrition.

  9. Electrodeposition of ZnO-doped films as window layer for Cd-free CIGS-based solar cells

    NASA Astrophysics Data System (ADS)

    Tsin, Fabien; Vénérosy, Amélie; Hildebrandt, Thibaud; Hariskos, Dimitrios; Naghavi, Negar; Lincot, Daniel; Rousset, Jean

    2016-02-01

    The Cu(In,Ga)Se2 (CIGS) thin film solar cell technology has made a steady progress within the last decade reaching efficiency up to 22.3% on laboratory scale, thus overpassing the highest efficiency for polycrystalline silicon solar cells. High efficiency CIGS modules employ a so-called buffer layer of cadmium sulfide CdS deposited by Chemical Bath Deposition (CBD), which presence and Cd-containing waste present some environmental concerns. A second potential bottleneck for CIGS technology is its window layer made of i-ZnO/ZnO:Al, which is deposited by sputtering requiring expensive vacuum equipment. A non-vacuum deposition of transparent conductive oxide (TCO) relying on simpler equipment with lower investment costs will be more economically attractive, and could increase competitiveness of CIGS-based modules with the mainstream silicon-based technologies. In the frame of Novazolar project, we have developed a low-cost aqueous solution photo assisted electrodeposition process of the ZnO-based window layer for high efficiency CIGS-based solar cells. The window layer deposition have been first optimized on classical CdS buffer layer leading to cells with efficiencies similar to those measured with the sputtered references on the same absorber (15%). The the optimized ZnO doped layer has been adapted to cadmium free devices where the CdS is replaced by chemical bath deposited zinc oxysulfide Zn(S,O) buffer layer. The effect of different growth parameters has been studied on CBD-Zn(S,O)-plated co-evaporated Cu(In,Ga)Se2 substrates provided by the Zentrum für Sonnenenergie-und Wasserstoff-Forschung (ZSW). This optimization of the electrodeposition of ZnO:Cl on CIGS/Zn(S,O) stacks led to record efficiency of 14%, while the reference cell with a sputtered (Zn,Mg)O/ZnO:Al window layer has an efficiency of 15.2%.

  10. [Tobacco cadmium health risk assessment and reduction techniques: A review].

    PubMed

    Cao, Chen-liang; Ma, Yi-bing; Li, Ju-mei; Wei, Dong-pu; Shi, Yi

    2015-04-01

    Tobacco is one of the cadmium accumulation and tolerance plants. Decreasing cadmium content of tobacco contributes to environmental safety and human health. Three aspects on tobacco cadmium research were reviewed in this paper, i.e. uptake and distribution of cadmium in tobacco, and health risk assessment of cadmium in tobacco and reduction measures. The current situations and existing challenges in the research field were discussed. The cadmium tolerance mechanisms of tobacco were reviewed, the factors on cadmium uptake were analyzed, and the general distribution of cadmium in tobacco was summarized. From the point of health risk assessment, the lack of cadmium limits in tobacco was identified, the recommended formula to calculate cadmium limits of tobacco based on atmosphere cadmium limits and digestion cadmium limits was provided and the cadmium limits of tobacco were estimated using each formula, and suggestions on cadmium limits in tobacco were presented. At last, we put forward several effective reduction measures to lower cadmium level in tobacco leaves.

  11. Cadmium sulfide-copper sulfide heterojunction cell research. Quarterly progress report, December 1, 1979-February 29, 1980

    SciTech Connect

    1980-07-01

    Attempts have been continued to increase the short circuit current in cells of enhanced open circuit voltage. Both deposition of copper on the surface of the Cu/sub 2/S layer and hydrogen plasma treatments have been attempted. To date, no significant increase in ultimate current has been achieved. Various changes in cell production procedure have been made with significant improvements in reproducibility. Improvements in the structure of (CdZn)S layers and resulting cell properties have been achieved using modified substrates based on NiFe. Improvement have been made to the capacitance measuring systems with a consequent gain in resolution, accuracy and reproducibility. Structural studies of the electron beam deposited glass have revealed the presence of cracking and experiments have been carried out to determine the optimum deposition conditions for producing defect-free coatings.

  12. Requirements specification for nickel cadmium battery expert system

    NASA Technical Reports Server (NTRS)

    1986-01-01

    The requirements for performance, design, test, and qualification of a computer program identified as NICBES, Nickel Cadmium Battery Expert System, is established. The specific spacecraft power system configuration selected was the Hubble Space Telescope (HST) Electrical Power System (EPS) Testbed. Power for the HST comes from a system of 13 Solar Panel Arrays (SPAs) linked to 6 Nickel Cadmium Batteries which are connected to 3 Busses. An expert system, NICBES, will be developed at Martin Marietta Aerospace to recognize a testbed anomaly, identify the malfunctioning component and recommend a course of action. Besides fault diagnosis, NICBES will be able to evaluate battery status, give advice on battery status and provide decision support for the operator. These requirements are detailed.

  13. Lithium-cupric sulfide cell

    SciTech Connect

    Cuesta, A.J.; Bump, D.D.

    1980-01-01

    Lithium cells have become the primary power source for cardiac pacemakers due to their reliability and longevity at low current drain rates. A lithium-cupric sulfide cell was developed which makes maximum use of the shape of a pacemaker's battery compartment. The cell has a stable voltage throughout 90% of its lifetime. It then drops to a second stable voltage before depletion. The voltage drop creates a small decrease in pacemaker rate, which alerts the physician to replace the pacemaker. No loss of capacity due to self-discharge as been seen to date, and cells have proven to be safe under extreme conditions. 2 refs.

  14. Molybdenum sulfide/carbide catalysts

    DOEpatents

    Alonso, Gabriel; Chianelli, Russell R.; Fuentes, Sergio; Torres, Brenda

    2007-05-29

    The present invention provides methods of synthesizing molybdenum disulfide (MoS.sub.2) and carbon-containing molybdenum disulfide (MoS.sub.2-xC.sub.x) catalysts that exhibit improved catalytic activity for hydrotreating reactions involving hydrodesulfurization, hydrodenitrogenation, and hydrogenation. The present invention also concerns the resulting catalysts. Furthermore, the invention concerns the promotion of these catalysts with Co, Ni, Fe, and/or Ru sulfides to create catalysts with greater activity, for hydrotreating reactions, than conventional catalysts such as cobalt molybdate on alumina support.

  15. Preparation of amorphous sulfide sieves

    DOEpatents

    Siadati, Mohammad H.; Alonso, Gabriel; Chianelli, Russell R.

    2006-11-07

    The present invention involves methods and compositions for synthesizing catalysts/porous materials. In some embodiments, the resulting materials are amorphous sulfide sieves that can be mass-produced for a variety of uses. In some embodiments, methods of the invention concern any suitable precursor (such as thiomolybdate salt) that is exposed to a high pressure pre-compaction, if need be. For instance, in some cases the final bulk shape (but highly porous) may be same as the original bulk shape. The compacted/uncompacted precursor is then subjected to an open-flow hot isostatic pressing, which causes the precursor to decompose and convert to a highly porous material/catalyst.

  16. Synthesis and optical properties of sulfide nanoparticles prepared in dimethylsulfoxide.

    PubMed

    Li, Yuebin; Ma, Lun; Zhang, Xing; Joly, Alan G; Liu, Zuli; Chen, Wei

    2008-11-01

    Many methods have been reported for the formation of sulfide nanoparticles by the reaction of metallic salts with sulfide chemical sources in aqueous solutions or organic solvents. Here, we report the formation of sulfide nanoparticles in dimethylsulfoxide (DMSO) by boiling metallic salts without sulfide sources. The sulfide sources are generated from the boiling of DMSO and react with metallic salts to form sulfide nanoparticles. In this method DMSO functions as a solvent and a sulfide source as well as a stabilizer for the formation of the nanoparticles. The recipe is simple and economical making sulfide nanoparticles formed in this way readily available for many potential applications.

  17. 40 CFR 425.03 - Sulfide analytical methods and applicability.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... Provisions § 425.03 Sulfide analytical methods and applicability. (a) The potassium ferricyanide titration... the potassium ferricyanide titration method for the determination of sulfide in wastewaters...

  18. 40 CFR 425.03 - Sulfide analytical methods and applicability.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... Provisions § 425.03 Sulfide analytical methods and applicability. (a) The potassium ferricyanide titration... the potassium ferricyanide titration method for the determination of sulfide in wastewaters...

  19. 40 CFR 425.03 - Sulfide analytical methods and applicability.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... Provisions § 425.03 Sulfide analytical methods and applicability. (a) The potassium ferricyanide titration... the potassium ferricyanide titration method for the determination of sulfide in wastewaters...

  20. Synthesis and Optical Properties of Sulfide Nanoparticles Prepared in Dimethylsulfoxide

    SciTech Connect

    Li, Yuebin; Ma, Lun; Zhang, Xing; Joly, Alan G.; Liu, Zuli; Chen, Wei

    2008-11-01

    Many methods have been reported for the formation of sulfide nanoparticles by the reaction of metallic salts with sulfide chemical sources in aqueous solutions or organic solvents. Here, we report the formation of sulfide nanoparticles in dimethylsulfoxide (DMSO) by boiling metallic salts without sulfide sources. The sulfide sources are generated from the boiling of DMSO and react with metallic salts to form sulfide nanoparticles. In this method DMSO functions as a solvent and a sulfide source as well as a stabilizer for the formation of the nanoparticles. The recipe is simple and economical making sulfide nanoparticles formed in this way readily available for many potential applications.

  1. Mechanisms of Cadmium Carcinogenesis [Abstract 2015

    EPA Science Inventory

    Cadmium is a transition metal and an ubiquitous environmental and industrial pollutant. Laboratory animal studies and epidemiological studies have shown that exposure to cadmium is associated with various organ toxicities and carcinogenic effects. Several national and internation...

  2. Cadmium-zinc interactions in plants and extractable cadmium and zinc fractions in soil

    SciTech Connect

    Abdel-Sabour, M.F.; Mortvedt, J.J.; Kelsoe, J.J.

    1988-06-01

    This study related Cd-Zn concentrations in plants to levels of Cd and Zn in soil recovered by several extractants soon after application of Cd and Zn sources to soil. Cadmium nitrate and ZnSO/sub 4/ or Zn(C/sub 2/H/sub 3/O/sub 2/)/sub 2/ were mixed with a Zn-deficient Crowley silt loam soil, cropped with corn (Zea mays L.), and then cropped with Swiss chard (Beta vulgaris). Applied Cd significantly increased the Cd/Zn ratio in both crops, especially in Swiss chard, which accumulates heavy metals. A previously published sequential-extraction procedure was used to fractionate Cd and Zn in soil after the corn harvest. Results of statistical analyses showed the highest correlation between Cd uptake by each crop and the carbonate and sulfide fractions of Cd in soil. Including other Cd fractions resulted in only slightly higher R/sup 2/ values. Zinc uptake by each crop was best related to the organic fraction of Zn in soil, and including the other Zn fractions did not affect the relationship. These results show that Cd and Zn uptake by corn or Swiss chard was not related to similar chemical fractions of these elements in soil, and that the Cd/Zn ratio in plant tops was significantly affected by both Cd and Zn applications to soil.

  3. Variation in sulfide tolerance of photosystem II in phylogenetically diverse cyanobacteria from sulfidic habitats

    NASA Technical Reports Server (NTRS)

    Miller, Scott R.; Bebout, Brad M.

    2004-01-01

    Physiological and molecular phylogenetic approaches were used to investigate variation among 12 cyanobacterial strains in their tolerance of sulfide, an inhibitor of oxygenic photosynthesis. Cyanobacteria from sulfidic habitats were found to be phylogenetically diverse and exhibited an approximately 50-fold variation in photosystem II performance in the presence of sulfide. Whereas the degree of tolerance was positively correlated with sulfide levels in the environment, a strain's phenotype could not be predicted from the tolerance of its closest relatives. These observations suggest that sulfide tolerance is a dynamic trait primarily shaped by environmental variation. Despite differences in absolute tolerance, similarities among strains in the effects of sulfide on chlorophyll fluorescence induction indicated a common mode of toxicity. Based on similarities with treatments known to disrupt the oxygen-evolving complex, it was concluded that sulfide toxicity resulted from inhibition of the donor side of photosystem II.

  4. Ammonia and hydrogen sulfide removal using biochar

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Reducing ammonia and hydrogen sulfide emissions from livestock facilities is an important issue for many communities and livestock producers. Ammonia has been regarded as odorous, precursor for particulate matter (PM), and contributed to livestock mortality. Hydrogen sulfide is highly toxic at elev...

  5. Sulfide oxidation under chemolithoautotrophic denitrifying conditions.

    PubMed

    Cardoso, Ricardo Beristain; Sierra-Alvarez, Reyes; Rowlette, Pieter; Flores, Elias Razo; Gómez, Jorge; Field, Jim A

    2006-12-20

    Chemolithoautotrophic denitrifying microorganisms oxidize reduced inorganic sulfur compounds coupled to the reduction of nitrate as an electron acceptor. These denitrifiers can be applied to the removal of nitrogen and/or sulfur contamination from wastewater, groundwater, and gaseous streams. This study investigated the physiology and kinetics of chemolithotrophic denitrification by an enrichment culture utilizing hydrogen sulfide, elemental sulfur, or thiosulfate as electron donor. Complete oxidation of sulfide to sulfate was observed when nitrate was supplemented at concentrations equal or exceeding the stoichiometric requirement. In contrast, sulfide was only partially oxidized to elemental sulfur when nitrate concentrations were limiting. Sulfide was found to inhibit chemolithotrophic sulfoxidation, decreasing rates by approximately 21-fold when the sulfide concentration increased from 2.5 to 10.0 mM, respectively. Addition of low levels of acetate (0.5 mM) enhanced denitrification and sulfate formation, suggesting that acetate was utilized as a carbon source by chemolithotrophic denitrifiers. The results of this study indicate the potential of chemolithotrophic denitrification for the removal of hydrogen sulfide. The sulfide/nitrate ratio can be used to control the fate of sulfide oxidation to either elemental sulfur or sulfate.

  6. 30 CFR 250.808 - Hydrogen sulfide.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 30 Mineral Resources 2 2011-07-01 2011-07-01 false Hydrogen sulfide. 250.808 Section 250.808 Mineral Resources BUREAU OF OCEAN ENERGY MANAGEMENT, REGULATION, AND ENFORCEMENT, DEPARTMENT OF THE... Safety Systems § 250.808 Hydrogen sulfide. Production operations in zones known to contain...

  7. Weathering of sulfides on Mars

    NASA Technical Reports Server (NTRS)

    Burns, Roger G.; Fisher, Duncan S.

    1987-01-01

    Pyrrhotite-pentlandite assemblages in mafic and ultramafic igneous rocks may have contributed significantly to the chemical weathering reactions that produce degradation products in the Martian regolith. By analogy and terrestrial processes, a model is proposed whereby supergene alteration of these primary Fe-Ni sulfides on Mars has generated secondary sulfides (e.g., pyrite) below the water table and produced acidic groundwater containing high concentrations of dissolved Fe, Ni, and sulfate ions. The low pH solutions also initiated weathering reactions of igneous feldspars and ferromagnesian silicates to form clay silicate and ferric oxyhydroxide phases. Near-surface oxidation and hydrolysis of ferric sulfato-and hydroxo-complex ions and sols formed gossan above the water table consisting of poorly crystalline hydrated ferric sulfates (e.g., jarosite), oxides (ferrihydrite, goethite), and silica (opal). Underlying groundwater, now permafrost contains hydroxo sulfato complexes of Fe, Al, Mg, Ni, which may be stabilized in frozen acidic solutions beneath the surface of Mars. Sublimation of permafrost may replenish colloidal ferric oxides, sulfates, and phyllosilicates during dust storms on Mars.

  8. Percutaneous absorption of selenium sulfide

    SciTech Connect

    Farley, J.; Skelly, E.M.; Weber, C.B.

    1986-01-01

    The purpose of this study was to determine selenium levels in the urine of Tinea patients before and after overnight application of a 2.5% selenium sulfide lotion. Selenium was measured by atomic absorption spectroscopy (AAS). Hydride generation and carbon rod atomization were studied. It was concluded from this study that selenium is absorbed through intact skin. Selenium is then excreted, at least partially, in urine, for at least a week following treatment. The data show that absorption and excretion of selenium vary on an individual basis. Selenium levels in urine following a single application of selenium sulfide lotion do not indicate that toxic amounts of selenium are being absorbed. Repeated treatments with SeS/sub 2/ result in selenium concentrations in urine which are significantly higher than normal. Significant matrix effects are observed in the carbon rod atomization of urine samples for selenium determinations, even in the presence of a matrix modifier such as nickel. The method of standard additions is required to obtain accurate results in the direct determination of selenium in urine by carbon rod AAS.

  9. Hydrogen sulfide pollution in wastewater treatment facilities

    SciTech Connect

    AlDhowalia, K.H. )

    1987-01-01

    The hydrogen sulfide (H{sub 2}S) found in wastewater collection systems and wastewater treatment facilities results from the bacterial reduction of the sulfate ion (SO{sub 4}). Hydrogen sulfide is a gas that occurs both in the sewer atmosphere and as a dissolved gas in the wastewater. When raw wastewater first enters the wastewater treatment facility by gravity most of the hydrogen sulfide is in the gaseous phase and will escape into the atmosphere at the inlet structures. Also some of the dissolved hydrogen sulfide will be released at points of turbulance such as at drops in flow, flumes, or aeration chambers. Several factors can cause excessive hydrogen sulfide concentrations in a sewerage system. These include septic sewage, long flow times in the sewerage system, high temperatures, flat sewer grades, and poor ventilation. These factors are discussed in this paper.

  10. 29 CFR 1928.1027 - Cadmium.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 29 Labor 9 2014-07-01 2014-07-01 false Cadmium. 1928.1027 Section 1928.1027 Labor Regulations...) OCCUPATIONAL SAFETY AND HEALTH STANDARDS FOR AGRICULTURE Occupational Health § 1928.1027 Cadmium. See § 1910.1027, Cadmium....

  11. 29 CFR 1928.1027 - Cadmium.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 29 Labor 9 2010-07-01 2010-07-01 false Cadmium. 1928.1027 Section 1928.1027 Labor Regulations...) OCCUPATIONAL SAFETY AND HEALTH STANDARDS FOR AGRICULTURE Occupational Health § 1928.1027 Cadmium. See § 1910.1027, Cadmium....

  12. 29 CFR 1928.1027 - Cadmium.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 29 Labor 9 2012-07-01 2012-07-01 false Cadmium. 1928.1027 Section 1928.1027 Labor Regulations...) OCCUPATIONAL SAFETY AND HEALTH STANDARDS FOR AGRICULTURE Occupational Health § 1928.1027 Cadmium. See § 1910.1027, Cadmium....

  13. Mechanisms of cadmium carcinogenesis

    SciTech Connect

    Joseph, Pius

    2009-08-01

    Cadmium (Cd), a heavy metal of considerable occupational and environmental concern, has been classified as a human carcinogen by the International Agency for Research on Cancer (IARC). The carcinogenic potential of Cd as well as the mechanisms underlying carcinogenesis following exposure to Cd has been studied using in vitro cell culture and in vivo animal models. Exposure of cells to Cd results in their transformation. Administration of Cd in animals results in tumors of multiple organs/tissues. Also, a causal relationship has been noticed between exposure to Cd and the incidence of lung cancer in human. It has been demonstrated that Cd induces cancer by multiple mechanisms and the most important among them are aberrant gene expression, inhibition of DNA damage repair, induction of oxidative stress, and inhibition of apoptosis. The available evidence indicates that, perhaps, oxidative stress plays a central role in Cd carcinogenesis because of its involvement in Cd-induced aberrant gene expression, inhibition of DNA damage repair, and apoptosis.

  14. Effect of ethylenediaminetetraacetic acid on the photocatalytic activities and flat-band potentials of cadmium sulfide and cadmium selenide

    SciTech Connect

    Uchihara, Toshio ); Matsumura, Michio; Ono, Junichi; Tsubomura, Hiroshi )

    1990-01-11

    Photocatalyzed hydrogen evolution on Pt-loaded CdS powder from aqueous solutions of sodium sulfite is enhanced by addition of a small amount of ethylenediaminetetraacetic acid (EDTA) to the solution. EDTA is hardly consumed by the reaction. It has been concluded from the measurements of the flat-band potential of CdS electrodes that EDTA and other chelating agents, such as 1,2-cyclohexanediaminetetraacetic acid and nitrilotriacetic acid, are adsorbed strongly on the surface of CdS and shift the conduction band energy toward the negative. The enhancement of the photocatalytic hydrogen evolution by the addition of EDTA is explained as being caused by the upward shift of the conduction band energy of CdS due to the negative charge of the chelating agents. The change of the conduction band energy by the adsorption of EDTA is observed also for CdSe electrodes. Although Pt-loaded CdSe powder is inactive for the hydrogen evolution from aqueous solutions of sodium sulfite, it generates hydrogen when EDTA is added to the solution.

  15. Hexamitiasis in cadmium-exposed mice.

    PubMed

    Exon, J H; Patton, N M; Koller, L D

    1975-09-01

    Mortality was observed in 4- to 5-week-old Swiss Webster mice exposed to 300 or 3 ppm cadmium as cadmium chloride in the drinking water. Mice receiving 300 ppm cadium suffered 26% mortality as compared with 7% of those on the low cadmium dose. Death did not occur in control mice. Clinical signs and histopathology established Hexamita muris as the causative agent. Cadmium lesions were not observed. It is suggested that mortality due to hexamitiasis resulted from synergism between cadmium and H muris.

  16. The effect of cadmium on the environment

    SciTech Connect

    Cole, J.F.; Volpe, R.

    1983-02-01

    Information on the effect of cadmium in the environment reported during the past several years has raised considerable questions about the validity of past conclusions. For example, it appears that the critical concentration of cadmium in the renal cortex may be significantly higher than previously thought, and also, there is growing evidence that cadmium was not responsible for Itai-Itai disease in Japan. These findings concerning cadmium are encouraging and indicate that while cadmium is certainly toxic, the new information should be considered by governmental authorities before steps are taken to enact overly stringent regulations based on assumptions and regulations that may no longer be correct.

  17. Nickel cadmium battery expert system

    NASA Technical Reports Server (NTRS)

    1986-01-01

    The applicability of artificial intelligence methodologies for the automation of energy storage management, in this case, nickel cadmium batteries, is demonstrated. With the Hubble Space Telescope Electrical Power System (HST/EPS) testbed as the application domain, an expert system was developed which incorporates the physical characterization of the EPS, in particular, the nickel cadmium batteries, as well as the human's operational knowledge. The expert system returns not only fault diagnostics but also status and advice along with justifications and explanations in the form of decision support.

  18. Arsenic-cadmium interaction in rats.

    PubMed

    Díaz-Barriga, F; Llamas, E; Mejía, J J; Carrizales, L; Santoyo, M E; Vega-Vega, L; Yáñez, L

    1990-11-01

    Simultaneous exposure to cadmium and arsenic is highly probable in the urban area of San Luis Potosi, Mexico due to common localization of copper and zinc smelters. Therefore, in this work, rats were intraperitoneally exposed either to cadmium or arsenic alone, or simultaneously to both metals. The effects of these treatments on three different toxicological parameters were studied. Cadmium modified the LD50 of arsenic and conversely arsenic modified the LD50 for cadmium. At the histopathological level, arsenic appeared to protect against the cadmium effects, especially on testes. This protective effect seemed to be related to the glutathione levels found in this tissue: rats exposed to both arsenic and cadmium, presented glutathione values intermediate to those observed after exposure to either metal alone; arsenic had the highest value and cadmium the lowest. In liver, rats exposed to arsenic, cadmium or arsenic and cadmium, presented glutathione values below those in the saline group, with the lowest value corresponding to the arsenic and cadmium treatment. The results appear to support the proposed interaction between arsenic and cadmium and coexposure to both metals seems to alter certain effects produced by either metal alone. PMID:2219140

  19. Determination of cadmium in biological samples.

    PubMed

    Klotz, Katrin; Weistenhöfer, Wobbeke; Drexler, Hans

    2013-01-01

    Analyses of cadmium concentrations in biological material are performed using inductively coupled plasma mass spectrometry (ICP-MS) and atomic absorption spectrometry (AAS), but also electrochemical methods, neutron activation analysis (NAA), and X-ray fluorescence spectrometry (XRF). The predominant sample matrices include blood, plasma, serum, and urine, as well as hair, saliva, and tissue of kidney cortex, lung, and liver. While cadmium in blood reveals rather the recent exposure situation, cadmium in urine reflects the body burden and is an indicator for the cumulative long term exposure.After chronic exposure, cadmium accumulates in the human body and causes kidney diseases, especially lesions of proximal tubular cells. A tubular proteinuria causes an increase in urinary excretion of microproteins. Excretions of retinol binding protein (RBP), β2-microglobulin (β2-M), and α1-microglobulin are validated biomarkers for analyzing cadmium effects. For this purpose, immunological procedures such as ELISA, and radio- and latex-immunoassays are used.However, proteinuria is not specific to cadmium, but can also occur after exposure to other nephrotoxic agents or due to various kidney diseases. In summary, cadmium in urine and blood are the most specific biomarkers of cadmium exposure. A combination of parameters of exposure (cadmium in blood, cadmium in urine) and parameters of effect (e.g., β2-M, RBP) is required to reveal cadmium-induced nephrological effects. PMID:23430771

  20. Sulfiding of hydrogel derived catalysts

    SciTech Connect

    Kemp, R.A.

    1991-11-05

    This patent describes a process for hydrotreating hydrocarbon feeds. It comprises contacting the feeds at a temperature in the range of from about 400{degrees} F. to about 850{degrees} F. and a pressure in the range of from about 400 psig to about 2500 psig with a catalyst having improved desulfurization activity prepared by incorporating an element selected from the group consisting of nickel, cobalt and mixtures thereof, and a heavy metal selected from the group consisting of molybdenum, tungsten and mixtures thereof, into an alumina hydrogel containing a phosphorous-containing compound, and sulfiding the catalyst with a gaseous sulfur compound at a temperature of at least about 900{degrees} F. for at least one hour.

  1. Pelletizing of sulfide molybdenite concentrates

    NASA Astrophysics Data System (ADS)

    Palant, A. A.

    2007-04-01

    The results of a pelletizing investigation using various binding components (water, syrup, sulfite-alcohol distillery grains, and bentonite) of the flotation sulfide molybdenite concentrate (˜84% MoS2) from the Mongolian deposit are discussed. The use of syrup provides rather high-strength pellets (>3 N/pellet or >300 g/pellet) of the required size (2 3 mm) for the consumption of 1 kg binder per 100 kg concentrate. The main advantage of the use of syrup instead of bentonite is that the molybdenum cinder produced by oxidizing roasting of raw ore materials is not impoverished due to complete burning out of the syrup. This fact exerts a positive effect on the subsequent hydrometallurgical process, decreasing molybdenum losses related to dump cakes.

  2. [Hydrogen sulfide and penile erection].

    PubMed

    Huang, Yi-Ming; Cheng, Yong; Jiang, Rui

    2012-09-01

    Hydrogen sulfide (H2S) is the third type of active endogenous gaseous signal molecule following nitric oxide (NO) and carbon monoxide (CO). In mammalians, H2S is mainly synthesized by two proteases, cystathionine-beta-synthase (CBS) and cystathionine-gamma-lyase (CSE). H2S plays an essential function of physiological regulation in vivo, and promotes penile erection by acting on the ATP-sensitive potassium channels to relax the vascular smooth muscle as well as by the synergistic effect with testosterone and NO to relax the corpus cavernosum smooth muscle (CCSM). At present, the selective phosphodiesterase type 5 (PDE5) inhibitor is mainly used for the treatment of erectile dysfunction (ED), but some ED patients fail to respond. Therefore, further studies on the mechanism of H2S regulating penile erection may provide a new way for the management of erectile dysfunction.

  3. Cadmium inhalation and male reproductive toxicity.

    PubMed

    Ragan, H A; Mast, T J

    1990-01-01

    Cadmium is a highly toxic element that is cumulative and has a long biological half-life in mammals. The severe toxicity of cadmium in man has been known for more than 100 years. Despite the knowledge that cadmium is toxic, only 20 human cases of poisoning via ingestion were recorded prior to 1941, whereas in the ensuing five-year period more than 680 cases of cadmium poisonings from accidental oral ingestion of this metal were documented. Some of the recorded effects of exposure to cadmium in laboratory animals include renal tubular damage, placental and testicular necrosis, structural and functional liver damage, osteomalacia, testicular tumors, teratogenic malformations, anemia, hypertension, pulmonary edema, chronic pulmonary emphysema, and induced deficiencies of iron, copper, and zinc. Some of these effects have also been observed in human after accidental exposures to cadmium oxide fumes and are characteristic of the syndrome described in Japan as Itai Itai disease in which ingestion of cadmium is the inciting chemical.

  4. Structural studies in limestone sulfidation

    SciTech Connect

    Fenouil, L.A.; Lynn, S.

    1993-05-01

    This study investigates the sulfidation of limestone at high temperatures (700--900{degree}C) as the first step in the design of a High-Temperature Coal-Gas Clean-Up system using millimeter-size limestone particles. Several workers have found that the rate of this reaction significantly decreases after an initial 10 to 15% conversion of CaCO{sub 3} to CaS. The present work attempts to explain this feature. It is first established that millimeter-size limestone particles do not sinter at temperatures up to the CaCO{sub 3} calcination point (899{degree}C at 1.03 bar CO{sub 2} partial pressure). It is then shown that CaS sinters rapidly at 750 to 900{degree}C if CO{sub 2} is present in the gas phase. Scanning Electron Microscope (SEM) photographs and Electron Dispersive Spectroscopy (EDS) data reveal that the CaS product layer sinters and forms a quasi-impermeable coating around the CaCO{sub 3} grains that greatly hinders more H{sub 2}S from reaching the still unreacted parts of the stone. Moreover, most of the pores initially present within the limestone structure begin to disappear or, at least, are significantly reduced in size. From then on, subsequent conversion is limited by diffusion of H{sub 2}S through the CaS layer, possibly by S{sup 2{minus}} ionic diffusion. The kinetics is then adequately described by a shrinking-core model, in which a sharp front of completely converted limestone is assumed to progress toward the center of the pellet. Finally, experimental evidence and computer simulations using simple sintering models suggest that the CaS sintering, responsible for the sharp decrease in the sulfidation rate, is surface-diffusion controlled.

  5. 21 CFR 73.2995 - Luminescent zinc sulfide.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 1 2014-04-01 2014-04-01 false Luminescent zinc sulfide. 73.2995 Section 73.2995... COLOR ADDITIVES EXEMPT FROM CERTIFICATION Cosmetics § 73.2995 Luminescent zinc sulfide. (a) Identity. The color additive luminescent zinc sulfide is zinc sulfide containing a copper activator....

  6. 21 CFR 73.2995 - Luminescent zinc sulfide.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 1 2012-04-01 2012-04-01 false Luminescent zinc sulfide. 73.2995 Section 73.2995... COLOR ADDITIVES EXEMPT FROM CERTIFICATION Cosmetics § 73.2995 Luminescent zinc sulfide. (a) Identity. The color additive luminescent zinc sulfide is zinc sulfide containing a copper activator....

  7. 21 CFR 73.2995 - Luminescent zinc sulfide.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 1 2013-04-01 2013-04-01 false Luminescent zinc sulfide. 73.2995 Section 73.2995... COLOR ADDITIVES EXEMPT FROM CERTIFICATION Cosmetics § 73.2995 Luminescent zinc sulfide. (a) Identity. The color additive luminescent zinc sulfide is zinc sulfide containing a copper activator....

  8. 21 CFR 73.2995 - Luminescent zinc sulfide.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 1 2010-04-01 2010-04-01 false Luminescent zinc sulfide. 73.2995 Section 73.2995... COLOR ADDITIVES EXEMPT FROM CERTIFICATION Cosmetics § 73.2995 Luminescent zinc sulfide. (a) Identity. The color additive luminescent zinc sulfide is zinc sulfide containing a copper activator....

  9. 21 CFR 177.2490 - Polyphenylene sulfide resins.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Polyphenylene sulfide resins. 177.2490 Section 177... Components of Articles Intended for Repeated Use § 177.2490 Polyphenylene sulfide resins. Polyphenylene sulfide resins (poly(1,4-phenylene sulfide) resins) may be safely used as coatings or components...

  10. Evaluation of metal/acid-volatile sulfide relationships in the prediction of metal bioaccumulation by benthic macroinvertebrates

    SciTech Connect

    Ankley, G.T.

    1996-12-01

    Recent studies have demonstrated that the toxicity of divalent cationic metals (cadmium, copper, lead, nickel, and zinc) in sediments can be controlled through binding to acid-volatile sulfide (AVS). When the molar concentration of AVS exceeds that of the metals (i.e., the metal/AVS ratio is less than unity), they exist predominantly as insoluble metal sulfides, which presumably are not biologically available. Thus, at metal/AVS ratios less than 1, toxicity of sediment-associated metals to benthic macro-invertebrates has not been observed. However, bioaccumulation may provide a more direct assessment of contaminant bioavailability than the presence or absence of toxicity. The purpose of this report is to comprehensively review available literature on metal bioaccumulation versus sediment metal/AVS relationships to further examine the tenet that AVS controls metal bioavailability. In all, 12 studies were evaluated; these ranged from short-term (10-d) laboratory experiments with metal-spiked or field-collected sediments containing cadmium, copper, lead, nickel, and/or zinc to long-term (> 1-year) field studies with sediments spiked with cadmium or zinc. Test organisms included mollusks, oligochaetes, polychaetes, amphipods, and midges. The preponderance of studies indicated reduced accumulation of metals at sediment metal/AVS ratios of less than 1. However, there were exceptions to this general observation, two of which occurred in short-term laboratory experiments with cadmium- or nickel-spiked sediments. In these studies there appeared to be a linear accumulation of metals with increasing sediment metal concentrations irrespective of the metal/AVS ratio. Although there is experimental evidence suggesting that significant bioaccumulation of metals does not occur when there is sufficient AVS available to bind them, the existence of data to the contrary indicates the need for further research into factors controlling the bioaccumulation of metals from sediments.

  11. Nanostructured lead sulfide: synthesis, structure and properties

    NASA Astrophysics Data System (ADS)

    Sadovnikov, S. I.; Gusev, A. I.; Rempel, A. A.

    2016-07-01

    The theoretical and experimental results of recent studies dealing with nanostructured lead sulfide are summarized and analyzed. The key methods for the synthesis of nanostructured lead sulfide are described. The crystal structure of PbS in nanopowders and nanofilms is discussed. The influence of the size of nanostructure elements on the optical and thermal properties of lead sulfide is considered. The dependence of the band gap of PbS on the nanoparticle (crystallite) size for powders and films is illustrated. The bibliography includes 222 references.

  12. Microbial control of hydrogen sulfide production

    SciTech Connect

    Montgomery, A.D.; Bhupathiraju, V.K.; Wofford, N.; McInerney, M.J.

    1995-12-31

    A sulfide-resistant strain of Thiobacillus denitrificans, strain F, prevented the accumulation of sulfide by Desulfovibrio desulfuricans when both organisms were grown in liquid medium. The wild-type strain of T. denitrificans did not prevent the accumulation of sulfide produced by D. desulfuricans. Strain F also prevented the accumulation of sulfide by a mixed population of sulfate-reducing bacteria enriched from an oil field brine. Fermentation balances showed that strain F stoichiometrically oxidized the sulfide produced by D. desulfuricans and the oil field brine enrichment to sulfate. The ability of a strain F to control sulfide production in an experimental system of cores and formation water from the Redfield, Iowa, natural gas storage facility was also investigated. A stable, sulfide-producing biofilm was established in two separate core systems, one of which was inoculated with strain F while the other core system (control) was treated in an identical manner, but was not inoculated with strain F. When formation water with 10 mM acetate and 5 mM nitrate was injected into both core systems, the effluent sulfide concentrations in the control core system ranged from 200 to 460 {mu}M. In the test core system inoculated with strain F, the effluent sulfide concentrations were lower, ranging from 70 to 110 {mu}M. In order to determine whether strain F could control sulfide production under optimal conditions for sulfate-reducing bacteria, the electron donor was changed to lactate and inorganic nutrients (nitrogen and phosphate sources) were added to the formation water. When nutrient-supplemented formation water with 3.1 mM lactate and 10 mM nitrate was used, the effluent sulfide concentrations of the control core system initially increased to about 3,800 {mu}M, and then decreased to about 1,100 {mu}M after 5 weeks. However, in the test core system inoculated with strain F, the effluent sulfide concentrations were much lower, 160 to 330 {mu}M.

  13. Silicate sulfidation and chemical differences between enstatite chondrites and Earth

    NASA Astrophysics Data System (ADS)

    Lehner, S. W.; Petaev, M. I.; Buseck, P. R.

    2013-12-01

    Isotopic similarity between the Earth-Moon system and enstatite chondrites (ECs) led to the idea that ECs were Earth's building blocks [1-3]. However, compared to Earth's mantle, ECs have low Fe0/Fe ratios, are enriched in volatile elements, and depleted in refractory lithophile elements and Mg [4]. Therefore, deriving Earth composition from ECs requires a loss of volatiles during or prior to accretion and sequestering a large fraction of Si in the deep Earth. Alternatively, the isotopic similarity between the Earth and ECs is explained by their formation from a common precursor that experienced different evolutionary paths resulting in the chemical difference [4]. The vestiges of such a precursor are still present in the unequilibrated ECs as FeO-rich silicates with O isotopic compositions identical to bulk ECs and Earth [5]. Conversion of such a precursor into the characteristic EC mineral assemblage requires high-temperature processing in an H-poor environment with high fS2 and fO2 close to that of the classic solar nebula [6], consistent with redox conditions inferred from Ti4+/Ti3+ ratios in EC pyroxene [7]. Under such conditions reaction of FeO-rich silicates with S-rich gas results in their replacement by the assemblage of FeO-poor silicates; Fe, Mg, Ca sulfides; free silica; and Si-bearing Fe,Ni metal alloy. The progressive sulfidation of ferromagnesian silicates in chondrules results in loss of Mg and addition of Fe, Mn, S, Na, K and, perhaps, other volatiles [6]. At the advanced stages of silicate sulfidation recorded in the metal-sulfide nodules [8], a portion of Si is reduced and dissolved in the Fe,Ni metal. This process is known to fractionate Si isotopes [9,10] and would explain the differences between the ECs and Earth's mantle [11]. The sulfidation of silicates also produces porous S-rich silica, a peculiar phase observed so far only in the ECs. It consists of a sinewy SiO2-rich framework enclosing numerous vesicles filled with beam

  14. Investigation on laboratory and pilot-scale airlift sulfide oxidation reactor under varying sulfide loading rate.

    PubMed

    Pokasoowan, Chanya; Kanitchaidecha, Wilawan; K C, Bal Krishna; Annachhatre, Ajit P

    2009-01-01

    Airlift bioreactor was established for recovering sulfur from synthetic sulfide wastewater under controlled dissolved oxygen condition. The maximum recovered sulfur was 14.49 g/day when sulfide loading rate, dissolved oxygen (DO) and pH values were 2.97 kgHS(-)/m(3)-day, 0.2-1.0 mg/L and 7.2-7.8, respectively. On the other hand, the increase in recovered sulfur reduced the contact surface of sulfide oxidizing bacteria which affects the recovery process. This effect caused to reduce the conversion of sulfide to sulfur. More recovered sulfur was produced at high sulfide loading rate due to the change of metabolic pathway of sulfide-oxidizing bacteria which prevented the toxicity of sulfide in the culture. The maximum activity in this system was recorded to be about 3.28 kgS/kgVSS-day. The recovered sulfur contained organic compounds which were confirmed by the results from XRD and CHN analyzer. Afterwards, by annealing the recovered sulfur at 120 degrees C for 24 hrs under ambient Argon, the percentage of carbon reduced from 4.44% to 0.30%. Furthermore, the percentage of nitrogen and hydrogen decreased from 0.79% and 0.48% to 0.00% and 0.14%, respectively. This result showed the success in increasing the purity of recovered sulfur by using the annealing technique. The pilot-scale biological sulfide oxidation process was carried out using real wastewater from Thai Rayon Industry in Thailand. The airlift reactor successfully removed sulfide more than 90% of the influent sulfide at DO concentration of less than 0.1 mg/L, whereas the elementary sulfur production was 2.37 kgS/m(3)-day at sulfide loading rate of 2.14 kgHS(-)/m(3)-day. The sulfur production was still increasing as the reactor had not yet reached its maximum sulfide loading rate. PMID:19085599

  15. Cadmium in Jamaican Bush Teas

    PubMed Central

    Hoo Fung, LA; Rattray, VR; Lalor, GC

    2014-01-01

    Samples of Jamaican plants used as bush teas were collected from households in high soil-cadmium (Cd) areas of central Jamaica and analysed by graphite furnace atomic absorption spectrophotometry for total cadmium and for cadmium extractable with a hot water brew as prepared for human consumption to determine their contribution to dietary cadmium exposure. The concentrations ranged from < 0.03 to 6.85 μg/g for total Cd, between 1 and 15% of which was extracted with a hot water brew. One cup (200 ml) of the teas examined was found to contain < 0.04–1.18 μg of Cd and would contribute 0.1 – 0.3 μg of Cd to a person's dietary intake. This is significantly below the provisional tolerable weekly intake (PTWI) of 7 μg Cd/kg body weight established by the World Health Organization (WHO). While this suggests that bush tea consumption does not contribute significantly to the PTWI, some of the teas examined exceed the WHO recommendation of less than 0.3 mg/kg Cd for medicinal plants. PMID:25303189

  16. Mercury Telluride and Cadmium Telluride

    NASA Technical Reports Server (NTRS)

    2004-01-01

    A semiconductor's usefulness is determined by how atoms are ordered within the crystal's underlying three-dimensional structure. While this mercury telluride and cadmium telluride alloy sample mixes completely in Earth -based laboratories, convective flows prevent them from mixing uniformly. In space, the ingredients mix more homogenously, resulting in a superior product.

  17. Sulfidation of iron at high temperatures and diffusion kinetics in ferrous sulfide

    SciTech Connect

    Danielewski, M.; Mrowec, S.; Stoklosa, A.

    1982-02-01

    The kinetics and mechanism of iron sulfidation have been studied as a function of temperature (950-1200 K) and sulfur pressure (10/sup -3/ 0.065 atm). It has been stated that a compact Fe/sub 1-y/ S scale on iron grows according to the parabolic rate law as a result of outward lattice diffusion of metal ions through cation vacancies. The activation energy of sulfidation increases with sulfur pressure and the 1/n exponent increases with temperature. This nontypical dependence of iron sulfidation kinetics on temperature and pressure results from the analogous effect of both these parameters on defect concentration in ferrous sulfide. The chemical diffusion coefficients, D/sub FeS/ , and diffusion coefficients of defects, D/sub d/ , in ferrous sulfide have been calculated on the basis of parabolic rate contacts of iron sulfidation and deviations from stoichiometry in ferrous sulfide. It has been shown that D/sub FeS/ is practically independent of cation vacancy concentration whereas the diffusion coefficient of defects depends strongly on that parameter. A comparison of self-diffusion coefficients of iron in Fe/sub 1-y/ S calculated from the kinetics of iron sulfidation to those obtained from radioisotopic studies indicates that within the range studied of temperatures and sulfur vapor pressures the outward diffusion of iron across the scale occurs preferentially along the c axis of columnar ferrous sulfide crystals.

  18. Chelation of cadmium.

    PubMed Central

    Andersen, O

    1984-01-01

    The toxicity of cadmium is determined by chelation reactions: in vivo, Cd2+ exists exclusively in coordination complexes with biological ligands, or with administered chelating agents. The Cd2+ ion has some soft character, but it is not a typical soft ion. It has a high degree of polarizability, and its complexes with soft ligands have predominantly covalent bond characteristics. Cd2+ forms the most stable complexes with soft donor atoms (S much greater than N greater than 0). The coordination stereochemistry of Cd2+ is unusually varied, including coordination numbers from 2 to 8. Even though the Cd2+ ion is a d10 ion, disturbed coordination geometries are often seen. Generally, the stability of complexes increases with the number of coordination groups contributed by the ligand; consequently, complexes of Cd2+ with polydentate ligands containing SH groups are very stable. Cd2+ in metallothionein (MT) is coordinated with 4 thiolate groups, and the log stability constant is estimated to 25.5. Complexes between Cd2+ and low molecular weight monodentate or bidentate ligands, e.g., free amino acids (LMW-Cd), seem to exist very briefly, and Cd2+ is rapidly bound to high molecular weight proteins, mainly serum albumin. These complexes (HMW-Cd) are rapidly scavenged from blood, mainly by the liver, and Cd2+ is redistributed to MT. After about 1 day the Cd-MT complex (MT-Cd) almost exclusively accounts for the total retained dose of Cd2+, independent of the route of exposure. MT-Cd is slowly transferred to and accumulated in kidney cortex. The acute toxicity and interorgan distribution of parenterally administered Cd2+ are strongly influenced by preceding MT induction, or decreased capacity for MT synthesis; however, the gastrointestinal (GI) uptake of Cd2+ seems unaffected by preceding MT induction resulting in considerable capacity for Cd2+ chelation in intestinal mucosa, and this finding indicates that endogenous MT is not involved in Cd2+ absorption. The toxicity of

  19. Ridding Groundwater of Hydrogen Sulfide. Part 1.

    ERIC Educational Resources Information Center

    Lochrane, Thomas G.

    1979-01-01

    This article is the first in a series reviewing the problems associated with hydrogen sulfide in drinking water sources. Discussion centers on identification of a cost-effective balance between aeration and chlorination treatment operations. (AS)

  20. Selenium sulfide: adjunctive therapy for tinea capitis.

    PubMed

    Allen, H B; Honig, P J; Leyden, J J; McGinley, K J

    1982-01-01

    Selenium sulfide lotion used as a shampoo has been shown to be an effective adjunctive agent to griseofulvin in the treatment of tinea capitis. Of 16 children with Trichophyton tonsurans infections 15 had negative fungal cultures at two weeks following a regimen of daily oral griseofulvin and selenium sulfide shampooing twice weekly. All patients treated with griseofulvin alone or in combination with either a bland shampoo or topical clotrimazole had positive cultures not only at the two-week interval but also as long as eight weeks later. In vitro analysis shows selenium sulfide to be sporicidal, correlating well with the in vivo observations. It is postulated that selenium sulfide usage may lessen the chances for spreading of infectious spores to other individuals.

  1. Modulation of cadmium bioaccumulation and enhancing cadmium tolerance in Pichia kudriavzevii by sodium chloride preincubation.

    PubMed

    Ma, Ning; Li, Chunsheng; Zhang, Dandan; Yu, Jinzhi; Xu, Ying

    2016-07-01

    Application of growing microorganisms for cadmium removal is limited by the sensitivity of living cells to cadmium. The effects of sodium chloride (NaCl) preincubation on the cadmium bioaccumulation and tolerance of Pichia kudriavzevii and Saccharomyces cerevisiae were investigated in this study. NaCl preincubation significantly reduced the intracellular and cell-surface cadmium bioaccumulation of P. kudriavzevii at both 6 and 20 mg L(-1) cadmium, while no obvious effect was observed in S. cerevisiae except that the intracellular cadmium bioaccumulation at 20 mg L(-1) cadmium was reduced obviously by 20-60 g L(-1)  NaCl. For both yeasts, the improved contents of protein and proline after NaCl preincubation contributed to the cadmium tolerance. The thiol contents in P. kudriavzevii under cadmium stress were alleviated by NaCl preincubation, which might be due to the decrease of intracellular cadmium bioaccumulation. NaCl preincubation enhanced the contents of glycerol and trehalose in P. kudriavzevii under cadmium stress, while no acceleration was observed in S. cerevisiae. The results suggested that NaCl preincubation could be applied in cadmium removal by growing P. kudriavzevii to increase the cadmium tolerance of the yeast. PMID:26753521

  2. Distribution of cadmium in the pearl oyster following exposure to cadmium in seawater

    SciTech Connect

    Francesconi, K.A. )

    1989-08-01

    Laboratory studies on the uptake of cadmium from seawater have shown that bivalve molluscs readily accumulated cadmium from this medium and that the relative concentrations of cadmium between viscera and muscle were always the same as those found in natural populations. These results suggested that in the natural environment seawater was a major source of cadmium for bivalve molluscs. Results of a recent study have indicated that seawater is not always the major contributor of cadmium to bivalve molluscs. These authors reported high levels of cadmium in the pearl oyster Pinctada albina albina, collected from Shark Bay in Western Australia, and noted that there was no correlation between cadmium concentrations in the oysters and cadmium concentrations in the surrounding seawater. Australia is one of several countries which have a maximum permissible level of cadmium in molluscs. The possibility that the pearl oyster, and perhaps other molluscs as well, may accumulate cadmium preferentially in different tissues depending upon the source of cadmium has important implications in the area of contaminants in marine foodstuffs. The present study reports the uptake and distribution of cadmium within P. albina albina when subjected to cadmium in seawater alone.

  3. Modulation of cadmium bioaccumulation and enhancing cadmium tolerance in Pichia kudriavzevii by sodium chloride preincubation.

    PubMed

    Ma, Ning; Li, Chunsheng; Zhang, Dandan; Yu, Jinzhi; Xu, Ying

    2016-07-01

    Application of growing microorganisms for cadmium removal is limited by the sensitivity of living cells to cadmium. The effects of sodium chloride (NaCl) preincubation on the cadmium bioaccumulation and tolerance of Pichia kudriavzevii and Saccharomyces cerevisiae were investigated in this study. NaCl preincubation significantly reduced the intracellular and cell-surface cadmium bioaccumulation of P. kudriavzevii at both 6 and 20 mg L(-1) cadmium, while no obvious effect was observed in S. cerevisiae except that the intracellular cadmium bioaccumulation at 20 mg L(-1) cadmium was reduced obviously by 20-60 g L(-1)  NaCl. For both yeasts, the improved contents of protein and proline after NaCl preincubation contributed to the cadmium tolerance. The thiol contents in P. kudriavzevii under cadmium stress were alleviated by NaCl preincubation, which might be due to the decrease of intracellular cadmium bioaccumulation. NaCl preincubation enhanced the contents of glycerol and trehalose in P. kudriavzevii under cadmium stress, while no acceleration was observed in S. cerevisiae. The results suggested that NaCl preincubation could be applied in cadmium removal by growing P. kudriavzevii to increase the cadmium tolerance of the yeast.

  4. Bioavailability and chronic toxicity of cadmium in sediment to the estuarine amphipod Leptocheirus plumulosus

    SciTech Connect

    DeWitt, T.H.; Swartz, R.C.; Hansen, D.J.; McGovern, D.; Berry, W.J.

    1996-12-01

    Numerous studies have demonstrated the efficacy of interstitial water metal concentrations and simultaneously extracted metals/acid-volatile sulfide (SEM/AVS) ratios in explaining the acute toxicity of sediment-associated metals to benthic organisms. However, no full life-cycle chronic marine or estuarine tests have been conducted for this purpose. In this study, cohorts of newborn amphipods, Leptocheirus plumulosus, were exposed to cadmium-spiked estuarine sediment for 28 d to determine effects on mortality, growth, and reproduction relative to interstitial water and SEM/AVS normalization. Seven treatments of cadmium were tested: 0 (control), 0.34, 0.74, 1.31, 1.55, 2.23, and 4.82 M SEM{sub Cd}/AVS ratios (measured concentrations). Interstitial water cadmium (IW{sub Cd}) and sediment concentrations of SEM{sub Cd} and AVS were monitored periodically and by depth during the exposure. When sediment SEM{sub Cd}/AVS ratios were {le} 1.55, mean IW{sub Cd} concentrations were less than the 96-h water-only cadmium LC50 for juvenile and subadult L. plumulosus, and mortality, growth, and reproduction were not affected. When SEM{sub Cd}/AVD ratios were {ge} 2.23, IW{sub Cd} concentrations were more than 100 times greater than the 96-h water-only cadmium LC50, and all amphipods died. These results are consistent with predictions of metal bioavailability from acute tests with metal-spiked sediments, i.e., that sediments with SEM{sub Cd}/AVS ratios < 1 are not toxic, while sediments with SEM{sub Cd}/AVS ratios > 1 may be toxic.

  5. Upper critical field of copper molybdenum sulfide

    NASA Technical Reports Server (NTRS)

    Alterovitz, S. A.; Woollam, J. A.

    1978-01-01

    The upper critical field of sintered and sputtered copper molybdenum sulfide Cu(x)Mo6S8 was measured and found to exceed the Werthamer, Helfand, and Hohenberg (1966) value for a type II superconductor characterized by dirty limit, weak isotropic electron phonon coupling, and no paramagnetic limiting. It is suggested that the enhancement results from anisotropy or clean limit or both. Other ternary molybdenum sulfides appear to show similar anomalies.

  6. Rapid Deposition Technology Holds the Key for the World's Largest Manufacturer of Thin-Film Solar Modules (Fact Sheet)

    SciTech Connect

    Not Available

    2013-08-01

    First Solar, Inc. has been collaborating with NREL since 1991, advancing its thin-film cadmium telluride solar technology to grow from a startup company to become one of the world's largest manufacturers of solar modules, and the world's largest manufacturer of thin-film solar modules.

  7. Cadmium content of plants as affected by soil cadmium concentration

    SciTech Connect

    Lehoczky, E.; Szabados, I.; Marth, P.

    1996-12-31

    Pot experiments were conducted in greenhouse conditions to study the effects of increasing cadmium (Cd) levels on biomass production and Cd contents in corn, (Zea mays L.), garlic (Allium sativum L.), and spinach (Spinacia oleracea L.). Plants were grown in two soil types: Eutric cambisol soil and A gleyic luvisol soil. Spinach proved to be the most sensitive to Cd treatments as its biomass considerably decreased with the increasing Cd levels. Cadmium contents of the three crops increased with increasing levels of Cd applications. Statistical differences were observed in the Cd contents of crops depending on soil type. With the same Cd rates, Cd tissue concentration of test plants grown in the strongly acidic Gleyic luvisol soil were many times higher than that of plants grown in a neutral Eutric cambisol soil. 14 refs., 4 tabs.

  8. Hydrogen sulfide and translational medicine

    PubMed Central

    Guo, Wei; Cheng, Ze-yu; Zhu, Yi-zhun

    2013-01-01

    Hydrogen sulfide (H2S) along with carbon monoxide and nitric oxide is an important signaling molecule that has undergone large numbers of fundamental investigations. H2S is involved in various physiological activities associated with the regulation of homeostasis, vascular contractility, pro- and anti-inflammatory activities, as well as pro- and anti-apoptotic activities etc. However, the actions of H2S are influenced by its concentration, reaction time, and cell/disease types. Therefore, H2S is a signaling molecule without definite effect. The use of existing H2S donors is limited because of the instant release and short lifetime of H2S. Thus, translational medicine involving the sustained and controlled release of H2S is of great value for both scientific and clinical uses. H2S donation can be manipulated by different ways, including where H2S is given, how H2S is donated, or the specific structures of H2S-releasing drugs and H2S donor molecules. This review briefly summarizes recent progress in research on the physiological and pathological functions of H2S and H2S-releasing drugs, and suggests hope for future investigations. PMID:24096643

  9. Hydrogen Sulfide as a Gasotransmitter

    PubMed Central

    Gadalla, Moataz M.; Snyder, Solomon H.

    2010-01-01

    Nitric oxide (NO) and carbon monoxide (CO) are well established as messenger molecules throughout the body, gasotransmitters, based on striking alterations in mice lacking the appropriate biosynthetic enzymes. Hydrogen sulfide (H2S) is even more chemically reactive, but till recently there was little definitive evidence for its physiologic formation. Cystathionine β-synthase (CBS, EC 4.2.1.22), and Cystathionine γ-lyase (CSE; EC 4.4.1.1), also known as cytathionase, can generate H2S from cyst(e)ine. Very recent studies with mice lacking these enzymes have established that CSE is responsible for H2S formation in the periphery, while in the brain CBS is the biosynthetic enzyme. Endothelial-derived relaxing factor (EDRF) activity is reduced 80% in the mesenteric artery of mice with deletion of CSE, establishing H2S as a major physiologic EDRF. H2S appears to signal predominantly by S-sulfhydrating cysteines in its target proteins, analogous to S-nitrosylation by NO. Whereas S-nitrosylation typically inhibits enzymes, S-sulfhydration activates them. S-nitrosylation basally affects 1–2% of its target proteins, while 10–25% of H2S target proteins are S-sulfhydrated. In summary, H2S appears to be a physiologic gasotransmitter of comparable importance to NO and CO. PMID:20067586

  10. Sea ducks and aquaculture: the cadmium connection.

    PubMed

    Bendell, L I

    2011-03-01

    Elevated concentrations of cadmium have been reported in the kidneys of sea ducks that forage along the Pacific Northwest, and cadmium has been postulated as a possible cause of population declines. The blue mussel (Mytilus spp.) which occurs in dense numbers on aquaculture structures and are a primary prey item for sea ducks also contain elevated cadmium concentrations. To determine if foraging on mussels associated with aquaculture structures could pose a toxicological risk to sea ducks, amounts of cadmium ingested per body weight per day by a representative sea duck species, the surf scoter (Melanitta perspicillata), were estimated and compared to the reported avian cadmium NOAEL (no observable adverse effect level) and LOAEL (lowest observable adverse effect level). Results indicate that in some locations within the Pacific Northwest, sea ducks could be exposed to toxicologically significant levels of cadmium associated with mussels foraged from aquaculture structures. This raises the possibility that such exposure could be contributing to observed population declines in these species.

  11. Cadmium resistance in Drosophila: a small cadmium binding substance

    SciTech Connect

    Jacobson, K.B.; Williams, M.W.; Richter, L.J.; Holt, S.E.; Hook, G.J.; Knoop, S.M.; Sloop, F.V.; Faust, J.B.

    1985-01-01

    A small cadmium-binding substance (CdBS) has been observed in adult Drosophila melanogaster that were raised for their entire growth cycle on a diet that contained 0.15 mM CdCl/sub 2/. Induction of CdBS was observed in strains that differed widely in their sensitivity of CdCl/sub 2/. This report describes the induction of CdBS and some of its characteristics. 17 refs., 4 figs., 1 tab.

  12. Tolerance to cadmium and cadmium-binding ligands in Great Salt Lake brine shrimp (Artemia salina)

    SciTech Connect

    Jayasekara, S.; Drown, D.B.; Sharma, R.P.

    1986-02-01

    Information on the accumulation of cadmium in cytosolic proteins of Great Lake brine shrimp (Artemia salina) was obtained from animals collected directly from the lake and also from animal hatched and maintained in three sublethal concentrations of cadmium (0.5, 2.0, 5.0 ppm) in saltwater aquaria. Brine shrimp growth under these conditions was monitored by measuring body lengths during a 7-day exposure period. Heat-stable, cadmium-binding ligands were isolated and identified by Sephadex G-75 chromatography and atomic absorption spectrophotometry. Cadmium was found to be equally distributed between high and low molecular weight proteins in animals collected from the lake and the 0.5 ppm cadmium group. There was also a slight growth stimulation noted in the 0.5-pm group. Higher cadmium incorporation was noted in low molecular weight fractions with increasing cadmium concentration in the exposure media. Low molecular weight fractions were also found to have high uv absorption characteristics at 250 nm and low absorption at 280 nm. Molecular weight of the cadmium-binding ligands was found to be 11,000 as estimated by the gel filtration method. De novo synthesis of this protein was increased as a function of cadmium concentration in the media. However, slow accumulation of cadmium in other protein fractions was also noticed in higher cadmium exposure groups, suggesting the existence of possible tolerance mechanisms in brine shrimp exposed to suspected acute cadmium concentrations.

  13. Cadmium in smoke particulates of regular and filter cigarettes containing low and high cadmium concentrations

    SciTech Connect

    Bache, C.A.; Reid, C.M.; Hoffman, D.; Adams, J.D.; Lisk, D.J.

    1986-03-01

    In the work reported, filter and nonfilter cigarettes were prepared from high-cadmium tobacco grown on a municipal sludge-amended soil or a low-cadmium tobacco grown on untreated soil alone. These were smoked by machine to determine the effectiveness of the cigarette filters in possibly reducing the quantities of cadmium in the mainstream smoke particulates.

  14. Metallothionein-like cadmium binding protein in rat testes administered with cadmium and selenium

    SciTech Connect

    Ohta, H.; Seki, Y.; Imamiya, S.

    1988-08-01

    It is well known that the testicular damage caused by acute cadmium toxicity are protected by simultaneous selenium administration with cadmium, and that the cadmium concentration in the testis increases remarkably as compared with that of only cadmium administration. The increased cadmium in the testis was found in the high molecular weight fraction containing selenium, and it has been thought that the shift of cadmium from the low molecular weight fraction to the high molecular weight fraction containing selenium is an important protection mechanism. However, the cadmium concentration in this high molecular weight fraction decreased with time, then re-shifted to the fraction of metallothionein, a low molecular weight protein having a protective effect against cadmium toxicity. While recently studying the cadmium binding protein, like metallothionein, in testes, it has been reported that the amino acid composition of cadmium binding protein in testis is not similar to that of the hepatic metallothionein. The present study was undertaken to clarify the properties of the increased cadmium binding protein in the testis protected by simultaneous selenium administration with cadmium.

  15. NEAR-CONTINUOUS MEASUREMENT OF HYDROGEN SULFIDE AND CARBONYL SULFIDE BY AN AUTOMATIC GAS CHROMATOGRAPH

    EPA Science Inventory

    An automatic gas chromatograph with a flame photometric detector that samples and analyzes hydrogen sulfide and carbonyl sulfide at 30-s intervals is described. Temperature programming was used to elute trace amounts of carbon disulfide present in each injection from a Supelpak-S...

  16. Cadmium content of umbilical cord blood

    SciTech Connect

    Rabinowitz, M.; Finch, H.

    1984-06-01

    Cadmium was measured in the umbilical cord blood at birth from 94 healthy babies. Samples were dried and ashed at low temperatures with an oxygen plasma prior to atomic absorption spectrometry. The concentration of cadmium ranged from 0.003 to 0.210 ..mu..g/dl, with a mean of 0.045 +/- 0.063 (SD). Blood lead, maternal smoking, and proximity of residence to automobile traffic were not statistically related to cadmium levels.

  17. Plasma cadmium and zinc in human hypertension.

    PubMed

    Thind, G S; Fischer, G M

    1976-11-01

    1. Plasma cadmium and zinc were determined by atomic absorption spectrophotometry in inferior venal caval or peripheral venous blood in thrity hypertensive patients and fifteen normal subjects. 2. The mean plasma cadium in hypertensive patients was significantly higher than in normal control subjects. 3. The plasma cadmium/zinc ratio was significantly greater in hypertensive patients. 4. There was a significant positive correlation between the plasma cadmium/zinc ratio and the mean arterial blood pressure.

  18. Microbial Responses to Environmentally Toxic Cadmium.

    PubMed

    Roane; Pepper

    1999-11-01

    We analyzed the soil microbial communities from one uncontaminated and two metal-impacted soils and found that while cadmium adversely affected the numbers of culturable bacteria in all soils, cadmium-resistant isolates were found from each of the soils. With exposure to 24 and 48 µg ml(-1) soluble cadmium, the metal-contaminated soil communities were more resistant than the uncontaminated soil community. In addition, in one metal-stressed soil, the resistant population became more resistant with increased cadmium levels. Ribosomal 16S DNA sequencing identified the isolates as Arthrobacter, Bacillus, or Pseudomonas spp. Further characterization demonstrated that two of the isolates were highly resistant to soluble cadmium with maximum resistance at 275 µg ml(-1) cadmium. These isolates were also resistant to a variety of antibiotics, namely ampicillin, gentamicin, penicillin, and streptomycin, but no overall correlation was found between enhanced antibiotic resistance and cadmium resistance. One Pseudomonas isolate H1 did become more resistant with increasing cadmium levels, suggesting a different resistance mechanism at high cadmium concentrations. PMID:10758182

  19. The Epigenetic Effects of Prenatal Cadmium Exposure.

    PubMed

    Vilahur, Nadia; Vahter, Marie; Broberg, Karin

    2015-06-01

    Prenatal exposure to the highly toxic and common pollutant cadmium has been associated with adverse effects on child health and development. However, the underlying biological mechanisms of cadmium toxicity remain partially unsolved. Epigenetic disruption due to early cadmium exposure has gained attention as a plausible mode of action, since epigenetic signatures respond to environmental stimuli and the fetus undergoes drastic epigenomic rearrangements during embryogenesis. In the current review, we provide a critical examination of the literature addressing prenatal cadmium exposure and epigenetic effects in human, animal, and in vitro studies. We conducted a PubMed search and obtained eight recent studies addressing this topic, focusing almost exclusively on DNA methylation. These studies provide evidence that cadmium alters epigenetic signatures in the DNA of the placenta and of the newborns, and some studies indicated marked sexual differences for cadmium-related DNA methylation changes. Associations between early cadmium exposure and DNA methylation might reflect interference with de novo DNA methyltransferases. More studies, especially those including environmentally relevant doses, are needed to confirm the toxicoepigenomic effects of prenatal cadmium exposure and how that relates to the observed health effects of cadmium in childhood and later life.

  20. Effects of dietary cadmium on mallard ducklings

    USGS Publications Warehouse

    Cain, B.W.; Sileo, L.; Franson, J.C.; Moore, J.

    1983-01-01

    Mallard (Anas platyrhynchos) ducklings were fed cadmium in the diet at 0, 5, 10, or 20 ppm from 1 day of age until 12 weeks of age. At 4-week intervals six males and six females from each dietary group were randomly selected, bled by jugular venipuncture, and necropsied. Significant decreases in packed cell volume (PCV) and hemoglobin (Hb) concentration and a significant increase in serum glutamic pyruvic transaminase (GPT) were found at 8 weeks of age in ducklings fed 20 ppm cadmium. Mild to severe kidney lesions were evident in ducklings fed 20 ppm cadmium for 12 weeks. No other blood chemistry measurement, hematological parameter, or tissue histopathological measurement indicated a reaction to cadmium ingestion. Body weight, liver weight, and the ratio of the femur weight to length were not affected by dietary cadmium. Femur cadmium concentration In all ducklings 12 weeks of age declined from the values detected at 4 and 8 weeks of age. Liver cadmium concentrations were significantly higher in relation to the increased dietary levels and in relation to the length of time the ducklings were fed the cadmium diets. At 12 weeks of age the cadmium concentration in liver tissue was twice that in the diet.

  1. Cadmium, metallothionein and renal tubular toxicity.

    PubMed

    Nordberg, M; Jin, T; Nordberg, G F

    1992-01-01

    Cadmium-induced nephrotoxicity develops at cadmium concentrations in the renal cortex of 10-300 micrograms/g wet weight. The actual concentration at which it develops depends on a number of factors, e.g., exposure route, chemical species of cadmium administered, rate of administration and simultaneous exposure to other metals. The role of these factors can be explained by a mechanism of cadmium nephrotoxicity in which both extracellular and intracellular metallothionein binding play an essential role. In reindeer used for human food, cadmium was shown to be bound to metallothionein-like proteins. If cadmium bound to such proteins enters the blood plasma via the gastrointestinal tract, this is of special toxicological significance. Metallothionein-bound cadmium in the plasma of experimental animals is efficiently transported to the kidney. Tubular dysfunction in the kidney following a normally tubulotoxic dose of cadmium bound to metallothionein was prevented by preinduction of metallothionein synthesis by small non-toxic doses of cadmium. PMID:1303954

  2. Cadmium telluride photovoltaic radiation detector

    DOEpatents

    Agouridis, D.C.; Fox, R.J.

    A dosimetry-type radiation detector is provided which employs a polycrystalline, chlorine-compensated cadmium telluride wafer fabricated to operate as a photovoltaic current generator used as the basic detecting element. A photovoltaic junction is formed in the wafer by painting one face of the cadmium telluride wafer with an n-type semi-conductive material. The opposite face of the wafer is painted with an electrically conductive material to serve as a current collector. The detector is mounted in a hermetically sealed vacuum containment. The detector is operated in a photovoltaic mode (zero bias) while DC coupled to a symmetrical differential current amplifier having a very low input impedance. The amplifier converts the current signal generated by radiation impinging upon the barrier surface face of the wafer to a voltage which is supplied to a voltmeter calibrated to read quantitatively the level of radiation incident upon the detecting wafer.

  3. Cadmium telluride photovoltaic radiation detector

    DOEpatents

    Agouridis, Dimitrios C.; Fox, Richard J.

    1981-01-01

    A dosimetry-type radiation detector is provided which employs a polycrystalline, chlorine-compensated cadmium telluride wafer fabricated to operate as a photovoltaic current generator used as the basic detecting element. A photovoltaic junction is formed in the wafer by painting one face of the cadmium telluride wafer with an n-type semiconductive material. The opposite face of the wafer is painted with an electrically conductive material to serve as a current collector. The detector is mounted in a hermetically sealed vacuum containment. The detector is operated in a photovoltaic mode (zero bias) while DC coupled to a symmetrical differential current amplifier having a very low input impedance. The amplifier converts the current signal generated by radiation impinging upon the barrier surface face of the wafer to a voltage which is supplied to a voltmeter calibrated to read quantitatively the level of radiation incident upon the detecting wafer.

  4. Continuous measurement of dissolved sulfide in sewer systems.

    PubMed

    Sutherland-Stacey, L; Corrie, S; Neethling, A; Johnson, I; Gutierrez, O; Dexter, R; Yuan, Z; Keller, J; Hamilton, G

    2008-01-01

    Sulfides are particularly problematic in the sewage industry. Hydrogen sulfide causes corrosion of concrete infrastructure, is dangerous at high concentrations and is foul smelling at low concentrations. Despite the importance of sulfide monitoring there is no commercially available system to quantify sulfide in waste water. In this article we report on our use of an in situ spectrometer to quantify bisulfide in waste water and additional analysis with a pH probe to calculate total dissolved sulfide. Our results show it is possible to use existing commercially available and field proven sensors to measure sulfide to mg/l levels continuously with little operator intervention and no sample preparation. PMID:18309215

  5. Animal adaptations for tolerance and exploitation of poisonous sulfide.

    PubMed

    Grieshaber, M K; Völkel, S

    1998-01-01

    Many aquatic animal species can survive sulfide exposure to some extent through oxidation of the sulfide, which results mainly in thiosulfate. In several species, sulfide oxidation is localized in the mitochondria and is accompanied by ATP synthesis. In addition, blood-based and intracellular compounds can augment sulfide oxidation. The formation of thiosulfate requires oxygen, which results in an increase in oxygen consumption of some species. If not all sulfide is detoxified, cytochrome C oxidase is inhibited. Under these conditions, a sulfide-dependent anaerobic energy metabolism commences. PMID:9558453

  6. Historical perspectives on cadmium toxicology

    SciTech Connect

    Nordberg, Gunnar F.

    2009-08-01

    The first health effects of cadmium (Cd) were reported already in 1858. Respiratory and gastrointestinal symptoms occurred among persons using Cd-containing polishing agent. The first experimental toxicological studies are from 1919. Bone effects and proteinuria in humans were reported in the 1940's. After World War II, a bone disease with fractures and severe pain, the itai-itai disease, a form of Cd-induced renal osteomalacia, was identified in Japan. Subsequently, the toxicokinetics and toxicodynamics of Cd were described including its binding to the protein metallothionein. International warnings of health risks from Cd-pollution were issued in the 1970's. Reproductive and carcinogenic effects were studied at an early stage, but a quantitative assessment of these effects in humans is still subject to considerable uncertainty. The World Health Organization in its International Program on Chemical Safety, WHO/IPCS (1992) (Cadmium. Environmental Health Criteria Document 134, IPCS. WHO, Geneva, 1-280.) identified renal dysfunction as the critical effect and a crude quantitative evaluation was presented. In the 1990's and 2000 several epidemiological studies have reported adverse health effects, sometimes at low environmental exposures to Cd, in population groups in Japan, China, Europe and USA (reviewed in other contributions to the present volume). The early identification of an important role of metallothionein in cadmium toxicology formed the basis for recent studies using biomarkers of susceptibility to development of Cd-related renal dysfunction such as gene expression of metallothionein in peripheral lymphocytes and autoantibodies against metallothionein in blood plasma. Findings in these studies indicate that very low exposure levels to cadmium may give rise to renal dysfunction among sensitive subgroups of human populations such as persons with diabetes.

  7. Influence of the phenols on the biogeochemical behavior of cadmium in the mangrove sediment.

    PubMed

    Li, Jian; Liu, Jingchun; Lu, Haoliang; Jia, Hui; Yu, Junyi; Hong, Hualong; Yan, Chongling

    2016-02-01

    Phenols exert a great influence on the dynamic process of Cd in the soil-plant interface. We investigated the influence of phenols on the biogeochemical behavior of cadmium in the rhizosphere of Avicennia marina (Forsk) Vierh. All combinations of four levels of cadmium (0, 1, 2 and 4 mg/kg DW) and two levels of phenol (0 and 15 mg/kg DW) were included in the experimental design. We found that phenols facilitated increasing concentrations of exchangeable cadmium (Ex-Cd), acid volatile sulfide (AVS) and reactive solid-phase Fe (II) in sediments, and iron in plants, but inhibited Cd accumulation in iron plaque and roots. The concentrations of AVS and reactive solid-phase Fe (II) were significantly positively correlated with Cd treatment. As for the biogeochemical behavior of Cd in mangrove sediments, this research revealed that phenols facilitated activation and mobility of Cd. They disturbed the "source-sink" balance of Cd and turned it into a "source", whilst decreasing Cd absorption in A. marina. Additionally, phenols facilitated iron absorption in the plant and alleviated the Fe limit for mangrove plant growth.

  8. FIB-TEM Investigations of Fe-NI-Sulfides in the CI Chondrites Alais and Orgueil

    NASA Technical Reports Server (NTRS)

    Berger, Eve L.; Lauretta, D. S.; Zega, T. J.; Keller, L. P.

    2013-01-01

    The CI chondrites are primitive meteorites with bulk compositions matching the solar photosphere for all but the lightest elements. They have been extensively aqueously altered, and are composed primarily of fine-grained phyllosilicate matrix material which is host to carbonates, sulfates, sulfides, and minor amounts of olivine and pyroxene. The alteration, while extensive, is heterogeneous. For example, CI-chondrite cubanite and carbonate grains differ on mm to sub-mm scales, demonstrating multiple aqueous episodes. CI-chondrite variability is also evidenced by degree of brecciation, abundance and size of coarse-grained phyllosilicates, olivine and pyroxene abundance, as well as Ni-content and size of sulfide grains. Our previous work revealed Orgueil sulfide grains with variable Ni-contents, metal:S ratios, crystal structures and textures. We continue to explore the variability of CI-chondrite pyrrhotite (Po, (FeNi)1-xS) and pentlandite (Pn, (Fe,Ni)9S8) grains. We investigate the microstructure of sulfides within and among CI-chondrite meteorites in order to place constraints on the conditions under which they formed.

  9. Hydrogen Sulfide Inhibits Amyloid Formation

    PubMed Central

    2015-01-01

    Amyloid fibrils are large aggregates of misfolded proteins, which are often associated with various neurodegenerative diseases such as Alzheimer’s, Parkinson’s, Huntington’s, and vascular dementia. The amount of hydrogen sulfide (H2S) is known to be significantly reduced in the brain tissue of people diagnosed with Alzheimer’s disease relative to that of healthy individuals. These findings prompted us to investigate the effects of H2S on the formation of amyloids in vitro using a model fibrillogenic protein hen egg white lysozyme (HEWL). HEWL forms typical β-sheet rich fibrils during the course of 70 min at low pH and high temperatures. The addition of H2S completely inhibits the formation of β-sheet and amyloid fibrils, as revealed by deep UV resonance Raman (DUVRR) spectroscopy and ThT fluorescence. Nonresonance Raman spectroscopy shows that disulfide bonds undergo significant rearrangements in the presence of H2S. Raman bands corresponding to disulfide (RSSR) vibrational modes in the 550–500 cm–1 spectral range decrease in intensity and are accompanied by the appearance of a new 490 cm–1 band assigned to the trisulfide group (RSSSR) based on the comparison with model compounds. The formation of RSSSR was proven further using a reaction with TCEP reduction agent and LC-MS analysis of the products. Intrinsic tryptophan fluorescence study shows a strong denaturation of HEWL containing trisulfide bonds. The presented evidence indicates that H2S causes the formation of trisulfide bridges, which destabilizes HEWL structure, preventing protein fibrillation. As a result, small spherical aggregates of unordered protein form, which exhibit no cytotoxicity by contrast with HEWL fibrils. PMID:25545790

  10. Hydrogen Sulfide and Urogenital Tract.

    PubMed

    di Villa Bianca, Roberta d'Emmanuele; Cirino, Giuseppe; Sorrentino, Raffaella

    2015-01-01

    In this chapter the role played by H2S in the physiopathology of urogenital tract revising animal and human data available in the current relevant literature is discussed. H2S pathway has been demonstrated to be involved in the mechanism underlying penile erection in human and experimental animal. Both cystathionine-β synthase (CBS) and cystathionine-γ lyase (CSE) are expressed in the human corpus cavernosum and exogenous H2S relaxes isolated human corpus cavernosum strips in an endothelium-independent manner. Hydrogen sulfide pathway also accounts for the direct vasodilatory effect operated by testosterone on isolated vessels. Convincing evidence suggests that H2S can influence the cGMP pathway by inhibiting the phosphodiesterase 5 (PDE-5) activity. All these findings taken together suggest an important role for the H2S pathway in human corpus cavernosum homeostasis. However, H2S effect is not confined to human corpus cavernosum but also plays an important role in human bladder. Human bladder expresses mainly CBS and generates in vitro detectable amount of H2S. In addition the bladder relaxant effect of the PDE-5 inhibitor sildenafil involves H2S as mediator. In conclusion the H2S pathway is not only involved in penile erection but also plays a role in bladder homeostasis. In addition the finding that it involved in the mechanism of action of PDE-5 inhibitors strongly suggests that modulation of this pathway can represent a therapeutic target for the treatment of erectile dysfunction and bladder diseases. PMID:26162831

  11. Growth analysis of cadmium sulfide thin films by atomic force microscopy

    SciTech Connect

    Moutinho, H.R.; Dhere, R.G.; Ramanathan, K.

    1996-05-01

    CdS films have been deposited by solution growth on SnO{sub 2} and glass substrates. Nucleation on SnO{sub 2} occurs at early deposition times, and complete conformal coverage is observed at low thickness values. The average grain size of the CdS films is established at these early times. In films deposited on glass substrates, nucleation is slower and occurs through 3-dimensional islands that increase in size and number as deposition proceeds. Optical measurements show that the bandgap values of CdS films deposited on SnO{sub 2} depend mainly on substrate structure. Hydrogen heat treatment does not affect the surface morphology of the samples, but decreases bandgap values.

  12. Toxicity of cadmium sulfide (CdS) nanoparticles against Escherichia coli and HeLa cells.

    PubMed

    Hossain, Sk Tofajjen; Mukherjee, Samir Kumar

    2013-09-15

    The present study endeavours to assess the toxic effect of synthesized CdS nanoparticles (NPs) on Escherichia coli and HeLa cells. The CdS NPs were characterized by DLS, XRD, TEM and AFM studies and the average size of NPs was revealed as ∼3 nm. On CdS NPs exposure bacterial cells changed morphological features to filamentous form and damage of the cell surface was found by AFM study. The expression of two conserved cell division components namely ftsZ and ftsQ in E. coli was decreased both at transcriptional and translational levels upon CdS NPs exposure. CdS NPs inhibited proper cell septum formation without affecting the nucleoid segregation. Viability of HeLa cells declined with increasing concentration of CdS NPs and the IC₅₀ value was found to be 4 μg/mL. NPs treated HeLa cells showed changed morphology with condensed and fragmented nuclei. Increased level of reactive oxygen species (ROS) was found both in E. coli and HeLa cells on CdS NPs exposure. The inverse correlation between declined cell viabilities and elevated ROS level suggested that oxidative stress seems to be the key event by which NPs induce toxicity both in E. coli and HeLa cells.

  13. Cadmium Sulfide Quantum Dots as a Fluorescent Probe for Quantitative Determination of Cefixime

    NASA Astrophysics Data System (ADS)

    Shah, J.; Rasul Jan, M.; Tasmia; Yousaf, M.

    2016-05-01

    Water-soluble fluorescent CdS quantum dots (QDs) capped with thioglycolic acid (TGA) were prepared. The resulting QDs have characteristic emission maximum at 514 nm after excitation at 370 nm. Fluorescent QDs were used for the quantification of cefixime based on its quenching effect on the fluorescence intensity of the QDs. Maximum fluorescence quenching was observed when 0.3 mM of QDs were mixed with cefixime and allowed to stand for 5 min. At optimum experimental conditions, the Stern-Volmer calibration plot of Fo/F against concentration of cefixime was linear in the range of 2-40 μg/mL. The limit of detection (3.3SD/b) and limit of quantification (10SD/b) were found to be 1.3 and 3.9 μg/mL respectively with RSD ≤ 1.56%. The proposed method was successfully applied to commercial formulations with % recovery in the range of 97.17 ± 1.16-100.15 ± 0.61.The results were compared with reference methods and evaluated statistically using student t-test and variance ratio F-test.

  14. Electrical and optoelectrical modification of cadmium sulfide nanobelts by low-energy electron beam irradiation

    NASA Astrophysics Data System (ADS)

    Zhang, Lijie; Liu, Manman; Zhao, Mei; Dong, Youqing; Zou, Chao; Yang, Keqin; Yang, Yun; Huang, Shaoming; Zhu, Da-Ming

    2016-09-01

    In this report, we describe a method for modifying electrical and optoelectrical properties of CdS nanobelts using low-energy (lower than 10 keV) e-beam irradiation in a scanning electron microscope. The electrical conductivity of the nanobelts was dramatically improved via the irradiation of e-beams. The modified conductivity of the nanobelts depends on the energy of the e-beam; it exhibits a larger photocurrent and higher external quantum efficiency but slower time-response than that before the modification. A possible mechanism about the modification is the increase of electron accumulation (injected electrons) in the nanobelts due to e-beam irradiation. In addition, the optoelectrical modification could be caused by the trapped electrons in the nanobelts and the decrease of contact resistance between the nanobelts and metal electrodes induced by e-beam irradiation. The results of this work are significant for the in situ study of semiconductor nanostructures in the electron microscope. Besides, the method of electrical and optoelectrical modification presented here has potential application in electronics and optoelectronics.

  15. Highly Efficient Photocatalytic Hydrogen Production of Flower-like Cadmium Sulfide Decorated by Histidine.

    PubMed

    Wang, Qizhao; Lian, Juhong; Li, Jiajia; Wang, Rongfang; Huang, Haohao; Su, Bitao; Lei, Ziqiang

    2015-01-01

    Morphology-controlled synthesis of CdS can significantly enhance the efficiency of its photocatalytic hydrogen production. In this study, a novel three-dimensional (3D) flower-like CdS is synthesized via a facile template-free hydrothermal process using Cd(NO3)2•4H2O and thiourea as precursors and L-Histidine as a chelating agent. The morphology, crystal phase, and photoelectrochemical performance of the flower-like CdS and pure CdS nanocrystals are carefully investigated via various characterizations. Superior photocatalytic activity relative to that of pure CdS is observed on the flower-like CdS photocatalyst under visible light irradiation, which is nearly 13 times of pure CdS. On the basis of the results from SEM studies and our analysis, a growth mechanism of flower-like CdS is proposed by capturing the shape evolution. The imidazole ring of L-Histidine captures the Cd ions from the solution, and prevents the growth of the CdS nanoparticles. Furthermore, the photocatalytic contrast experiments illustrate that the as-synthesized flower-like CdS with L-Histidine is more stable than CdS without L-Histidine in the hydrogen generation. PMID:26337119

  16. Review of methods for preparatin of zinc and cadmium sulfide, selenide and telluride single cyrstals

    NASA Technical Reports Server (NTRS)

    Kucharczyk, M.; Zabludowska, K.

    1986-01-01

    The growth method of (Zn,Cd)S, (Zn,Cd)Se, (Zn,Cd)Te single crystals is reviewed. It is suggested that the method of sublimation-condensation is the most suitable to the conditions and facilities available, and should be employed in the Department of Physics of Bislystok Polytechnic.

  17. Preparation of manganese doped cadmium sulfide nanoparticles in zincblende phase and their magnetic properties.

    PubMed

    Nakaya, Masafumi; Tanaka, Itaru; Muramatsu, Atsushi

    2012-12-01

    In this study, the random dope of Mn into CdS nanoparticles in zincblende phase has been carried out under the mild reaction condition. The resulting nanoparticles were characterized by energy dispersive X-ray analysis (EDX), transmission electron microscopy (TEM), X-ray diffractometer (XRD), UV-Vis spectrometer, PL spectrometer, and SQUID. EDX showed that the compositions of Mn doped CdS nanoparticles were readily controlled. TEM showed the particle sizes were not significantly affected by the compositions, retaining to be ca. 3 nm with a narrow size distribution. UV-Vis and PL spectra of the resulting nanoparticles showed the intra-Mn level may be affected by the quantum size effect. SQUID measurement showed that the resulting nanoparticles showed diamagnetism, paramagnetism and superparamagnetism dependent on Mn content. PMID:23447951

  18. Highly Efficient Photocatalytic Hydrogen Production of Flower-like Cadmium Sulfide Decorated by Histidine

    PubMed Central

    Wang, Qizhao; Lian, Juhong; Li, Jiajia; Wang, Rongfang; Huang, Haohao; Su, Bitao; Lei, Ziqiang

    2015-01-01

    Morphology-controlled synthesis of CdS can significantly enhance the efficiency of its photocatalytic hydrogen production. In this study, a novel three-dimensional (3D) flower-like CdS is synthesized via a facile template-free hydrothermal process using Cd(NO3)2•4H2O and thiourea as precursors and L-Histidine as a chelating agent. The morphology, crystal phase, and photoelectrochemical performance of the flower-like CdS and pure CdS nanocrystals are carefully investigated via various characterizations. Superior photocatalytic activity relative to that of pure CdS is observed on the flower-like CdS photocatalyst under visible light irradiation, which is nearly 13 times of pure CdS. On the basis of the results from SEM studies and our analysis, a growth mechanism of flower-like CdS is proposed by capturing the shape evolution. The imidazole ring of L-Histidine captures the Cd ions from the solution, and prevents the growth of the CdS nanoparticles. Furthermore, the photocatalytic contrast experiments illustrate that the as-synthesized flower-like CdS with L-Histidine is more stable than CdS without L-Histidine in the hydrogen generation. PMID:26337119

  19. Electrical and optoelectrical modification of cadmium sulfide nanobelts by low-energy electron beam irradiation.

    PubMed

    Zhang, Lijie; Liu, Manman; Zhao, Mei; Dong, Youqing; Zou, Chao; Yang, Keqin; Yang, Yun; Huang, Shaoming; Zhu, Da-Ming

    2016-09-30

    In this report, we describe a method for modifying electrical and optoelectrical properties of CdS nanobelts using low-energy (lower than 10 keV) e-beam irradiation in a scanning electron microscope. The electrical conductivity of the nanobelts was dramatically improved via the irradiation of e-beams. The modified conductivity of the nanobelts depends on the energy of the e-beam; it exhibits a larger photocurrent and higher external quantum efficiency but slower time-response than that before the modification. A possible mechanism about the modification is the increase of electron accumulation (injected electrons) in the nanobelts due to e-beam irradiation. In addition, the optoelectrical modification could be caused by the trapped electrons in the nanobelts and the decrease of contact resistance between the nanobelts and metal electrodes induced by e-beam irradiation. The results of this work are significant for the in situ study of semiconductor nanostructures in the electron microscope. Besides, the method of electrical and optoelectrical modification presented here has potential application in electronics and optoelectronics. PMID:27561004

  20. Improvement of the luminescent properties of cadmium sulfide quantum dots by a post-synthesis modification

    NASA Astrophysics Data System (ADS)

    López, Israel; Gómez, Idalia

    2014-11-01

    Here the improvement of the luminescent properties of CdS quantum dots by a post-synthesis modification with aqueous solutions of NaOH at different concentrations is presented. The CdS quantum dots were synthesized by a microwave-assisted method using citrate ions as stabilizer. The addition of the hydroxide ions increased the intensity of the orange-red emission by about 80%. Besides, a violet-blue emission was achieved by means of this post-synthesis modification. The hydroxide ions control the precipitation equilibria of the CdS and Cd(OH)2, dissolving and precipitating the surface of the quantum dots. The NaOH treatment increases the number of traps, which produces less band-edge and more deep-trap emission, which explains the decrease and increase in the intensity of the violet-blue and orange-red emissions, respectively.

  1. Small angle X-ray and neutron scattering on cadmium sulfide nanoparticles in silicate glass

    NASA Astrophysics Data System (ADS)

    Kuznetsova, Yu. V.; Rempel, A. A.; Meyer, M.; Pipich, V.; Gerth, S.; Magerl, A.

    2016-08-01

    Small angle X-ray and neutron scattering on Cd and S doped glass annealed at 600 °C shows after the first 12 h nucleation and growth of spherical CdS nanoparticles with a radius of up to 34±4 Å. After the nucleation is completed after 24 h, further growth in this amorphous environment is governed by oriented particle attachment mechanism as found for a liquid medium. Towards 48 h the particle shape has changed into spheroidal with short and long axis of 40±2 Å and 120±2 Å, respectively.

  2. Evaluation of radiation interference in the Voyager Sun Sensor's cadmium sulfide detector

    NASA Technical Reports Server (NTRS)

    Clarke, T. C.; Divita, E. L.

    1978-01-01

    The simulation of radiation interference effects and the results of a radiation interference test on two Voyager Sun Sensor prototype detector assemblies are reported. The derivation of test levels and requirements are discussed and show that cobalt 60 gamma radiation is an effective and practical simulator of the ionization dose rate effects induced by high-energy electron flux incident on the spacecraft at a rate of 3.7 x 10 to the 8th e/sq cm-sec (10 rad(Si)/s) during closest approach to Jupiter. The test results provide information that is used to confirm an analytic correlation, and to predict satisfactory performance of a spacecraft sun sensing device having stringent angular resolution requirements. The measured detector response shows that at dose rates incident on the detector elements of 2 rad(Si)/sec, which is four times that expected during Jupiter encounter, the radiation-induced angle error is almost an order of magnitude less than that allowed by the acceptance criteria.

  3. Sulfide capacities of fayalite-base slags

    NASA Astrophysics Data System (ADS)

    Simeonov, S. R.; Sridhar, R.; Toguri, J. M.

    1995-04-01

    The sulfide capacities of fayalite-base slags were measured by a gas-slag equilibration technique under controlled oxygen and sulfur potentials similar to those encountered in the pyrometallurgical processing of nonferrous metals. The oxygen pressure range was from 10-9.5 to 10-11 MPa and the sulfur pressure range from 10-3 to 10-4.5 MPa, over a temperature range of 1473 to 1623 K. The slags studied were FeO-SiO2 at silica saturation and those with addition of CaO, MgO, and Al2O3 to determine their effect on sulfide capacities. For these slags, the sulfide capacities were found to vary from 10-3.3 to 10-5. The sulfide capacities increased with increasing temperature from 1473 to 1623 K. A comparison of the reported plant data on sulfur content of industrial slags shows good agreement with the present experimental results. The present data will be useful in estimating metal losses in slag due to metal sulfide entrainment in nonferrous smelters.

  4. Phase Engineering of 2D Tin Sulfides.

    PubMed

    Mutlu, Zafer; Wu, Ryan J; Wickramaratne, Darshana; Shahrezaei, Sina; Liu, Chueh; Temiz, Selcuk; Patalano, Andrew; Ozkan, Mihrimah; Lake, Roger K; Mkhoyan, K A; Ozkan, Cengiz S

    2016-06-01

    Tin sulfides can exist in a variety of phases and polytypes due to the different oxidation states of Sn. A subset of these phases and polytypes take the form of layered 2D structures that give rise to a wide host of electronic and optical properties. Hence, achieving control over the phase, polytype, and thickness of tin sulfides is necessary to utilize this wide range of properties exhibited by the compound. This study reports on phase-selective growth of both hexagonal tin (IV) sulfide SnS2 and orthorhombic tin (II) sulfide SnS crystals with diameters of over tens of microns on SiO2 substrates through atmospheric pressure vapor-phase method in a conventional horizontal quartz tube furnace with SnO2 and S powders as the source materials. Detailed characterization of each phase of tin sulfide crystals is performed using various microscopy and spectroscopy methods, and the results are corroborated by ab initio density functional theory calculations. PMID:27099950

  5. Phase Engineering of 2D Tin Sulfides.

    PubMed

    Mutlu, Zafer; Wu, Ryan J; Wickramaratne, Darshana; Shahrezaei, Sina; Liu, Chueh; Temiz, Selcuk; Patalano, Andrew; Ozkan, Mihrimah; Lake, Roger K; Mkhoyan, K A; Ozkan, Cengiz S

    2016-06-01

    Tin sulfides can exist in a variety of phases and polytypes due to the different oxidation states of Sn. A subset of these phases and polytypes take the form of layered 2D structures that give rise to a wide host of electronic and optical properties. Hence, achieving control over the phase, polytype, and thickness of tin sulfides is necessary to utilize this wide range of properties exhibited by the compound. This study reports on phase-selective growth of both hexagonal tin (IV) sulfide SnS2 and orthorhombic tin (II) sulfide SnS crystals with diameters of over tens of microns on SiO2 substrates through atmospheric pressure vapor-phase method in a conventional horizontal quartz tube furnace with SnO2 and S powders as the source materials. Detailed characterization of each phase of tin sulfide crystals is performed using various microscopy and spectroscopy methods, and the results are corroborated by ab initio density functional theory calculations.

  6. Nephropathy in cadmium workers: assessment of risk from airborne occupational exposure to cadmium.

    PubMed Central

    Thun, M J; Osorio, A M; Schober, S; Hannon, W H; Lewis, B; Halperin, W

    1989-01-01

    To assess the quantitative relation between exposure to airborne cadmium and various markers of renal tubular and glomerular function, 45 male workers employed at a plant that recovers cadmium from industrial waste and 32 male hospital workers of similar age and geographical location were examined. Cumulative external exposure to airborne cadmium (dose) was estimated from historical air sampling data, adjusted for respirator use. Increasing cadmium dose was associated with multiple renal tubular functional abnormalities, including reduced reabsorption of beta-2-microglobulin (beta-2), retinol binding protein (RBP), calcium, and phosphate. Serum creatinine concentration also increased with cadmium dose, suggesting impaired glomerular function. Mean systolic and diastolic blood pressures were higher in the cadmium workers than in the unexposed (134 v 120 mm Hg and 80 v 73 mm Hg respectively), but only systolic blood pressure was significantly associated with cadmium dose in multivariate analyses. Cadmium dose remained the most important predictor of serum creatinine concentration after controlling for age, blood pressure, body size, and other extraneous factors. Logistic regression to model the probability (prevalence) of various renal abnormalities with increasing dose of cadmium was used. The probability of multiple tubular abnormalities and raised serum creatinine concentration increased sharply at cumulative cadmium exposures exceeding 300 mg/m3 days, corresponding to working for 4.3 years at the current permissible United States exposure limit for cadmium dust. PMID:2818957

  7. Improvement of cadmium phytoremediation after soil inoculation with a cadmium-resistant Micrococcus sp.

    PubMed

    Sangthong, Chirawee; Setkit, Kunchaya; Prapagdee, Benjaphorn

    2016-01-01

    Cadmium-resistant Micrococcus sp. TISTR2221, a plant growth-promoting bacterium, has stimulatory effects on the root lengths of Zea mays L. seedlings under toxic cadmium conditions compared to uninoculated seedlings. The performance of Micrococcus sp. TISTR2221 on promoting growth and cadmium accumulation in Z. mays L. was investigated in a pot experiment. The results indicated that Micrococcus sp. TISTR2221significantly promoted the root length, shoot length, and dry biomass of Z. mays L. transplanted in both uncontaminated and cadmium-contaminated soils. Micrococcus sp. TISTR2221 significantly increased cadmium accumulation in the roots and shoots of Z. mays L. compared to uninoculated plants. At the beginning of the planting period, cadmium accumulated mainly in the shoots. With a prolonged duration of cultivation, cadmium content increased in the roots. As expected, little cadmium was found in maize grains. Soil cadmium was significantly reduced with time, and the highest percentage of cadmium removal was found in the bacterial-inoculated Z. mays L. after transplantation for 6 weeks. We conclude that Micrococcus sp. TISTR2221 is a potent bioaugmenting agent, facilitating cadmium phytoextraction in Z. mays L. PMID:26336850

  8. Improvement of cadmium phytoremediation after soil inoculation with a cadmium-resistant Micrococcus sp.

    PubMed

    Sangthong, Chirawee; Setkit, Kunchaya; Prapagdee, Benjaphorn

    2016-01-01

    Cadmium-resistant Micrococcus sp. TISTR2221, a plant growth-promoting bacterium, has stimulatory effects on the root lengths of Zea mays L. seedlings under toxic cadmium conditions compared to uninoculated seedlings. The performance of Micrococcus sp. TISTR2221 on promoting growth and cadmium accumulation in Z. mays L. was investigated in a pot experiment. The results indicated that Micrococcus sp. TISTR2221significantly promoted the root length, shoot length, and dry biomass of Z. mays L. transplanted in both uncontaminated and cadmium-contaminated soils. Micrococcus sp. TISTR2221 significantly increased cadmium accumulation in the roots and shoots of Z. mays L. compared to uninoculated plants. At the beginning of the planting period, cadmium accumulated mainly in the shoots. With a prolonged duration of cultivation, cadmium content increased in the roots. As expected, little cadmium was found in maize grains. Soil cadmium was significantly reduced with time, and the highest percentage of cadmium removal was found in the bacterial-inoculated Z. mays L. after transplantation for 6 weeks. We conclude that Micrococcus sp. TISTR2221 is a potent bioaugmenting agent, facilitating cadmium phytoextraction in Z. mays L.

  9. Rapid Deposition Technology Holds the Key for the World's Largest Solar Manufacturer (Fact Sheet)

    SciTech Connect

    Not Available

    2010-10-01

    Thanks in part to years of collaboration with the National Renewable Energy Laboratory (NREL), a manufacturer of thin-film solar modules has grown from a small garage-type operation to become the world's largest manufacturer of solar modules. First Solar, Inc. now manufactures cadmium telluride (CdTe) solar modules throughout the world, but it began in Ohio as a small company called Solar Cells, Inc.

  10. Cadmium sulfate application to sludge-amended soils: II. Extraction of Cd, Zn, and Ma from solid phases

    SciTech Connect

    Mahler, R.J. ); Ryan, J.A. )

    1988-01-01

    Cadmium, Zn and Mn in eleven paired soils (one which had a history of sludge application and a control from adjacent land where sludge had not been used) were partitioned into five fractions: exchangeable, adsorbed, organically bound, carbonate bound and sulfide, by the use of KNO{sub 3}, H{sub 2}O, NaHO, EDTA and HNO{sub 3}, respectively. The data indicate that the major portion of the total metals was found in the carbonate, sulfide and organic fractions. Addition of CaCO{sub 3} caused an increase in the exchangeable + soluble fractions of added Cd in the soils, but had little effect on native or sludge derived Cd.

  11. A Photoelectrochemical Solar Cell: An Undergraduate Experiment.

    ERIC Educational Resources Information Center

    Boudreau, Sharon M.; And Others

    1983-01-01

    Preparation and testing of a cadmium selenide photoelectrical solar cell was introduced into an environmental chemistry course to illustrate solid state semiconductor and electrochemical principles. Background information, procedures, and results are provided for the experiment which can be accomplished in a three- to four-hour laboratory session…

  12. 40 CFR 425.03 - Sulfide analytical methods and applicability.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... § 425.03 Sulfide analytical methods and applicability. (a) The potassium ferricyanide titration method... ferricyanide titration method for the determination of sulfide in wastewaters discharged by plants operating...

  13. 40 CFR 425.03 - Sulfide analytical methods and applicability.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... § 425.03 Sulfide analytical methods and applicability. (a) The potassium ferricyanide titration method... ferricyanide titration method for the determination of sulfide in wastewaters discharged by plants operating...

  14. Preparation of silver-activated zinc sulfide thin films

    NASA Technical Reports Server (NTRS)

    Feldman, C.; Swindells, F. E.

    1968-01-01

    Silver improves luminescence and reduces contamination of zinc sulfide phosphors. The silver is added after the zinc sulfide phosphors are deposited in thin films by vapor evaporation, but before calcining, by immersion in a solution of silver salt.

  15. Mechanisms of hydrogen sulfide removal with steel making slag.

    PubMed

    Kim, Kyunghoi; Asaoka, Satoshi; Yamamoto, Tamiji; Hayakawa, Shinjiro; Takeda, Kazuhiko; Katayama, Misaki; Onoue, Takasumi

    2012-09-18

    In the present study, we experimentally investigated the removal of hydrogen sulfide using steel-making slag (SMS) and clarified the mechanism of hydrogen sulfide removal with the SMS. The results proved that SMS is able to remove hydrogen sulfide dissolved in water, and the maximum removal amount of hydrogen sulfide per unit weight of the SMS for 8 days was estimated to be 37.5 mg S/g. The removal processes of hydrogen sulfide were not only adsorption onto the SMS, but oxidation and precipitation as sulfur. The chemical forms of sulfide adsorbed onto the SMS were estimated to be sulfur and manganese sulfide in the ratio of 81% and 19%, respectively. It is demonstrated here that the SMS is a promising material to remediate organically enriched coastal sediments in terms of removal of hydrogen sulfide. Furthermore, using SMS is expected to contribute to development of a recycling-oriented society.

  16. Sulfide and methane production in sewer sediments.

    PubMed

    Liu, Yiwen; Ni, Bing-Jie; Ganigué, Ramon; Werner, Ursula; Sharma, Keshab R; Yuan, Zhiguo

    2015-03-01

    Recent studies have demonstrated significant sulfide and methane production by sewer biofilms, particularly in rising mains. Sewer sediments in gravity sewers are also biologically active; however, their contribution to biological transformations in sewers is poorly understood at present. In this study, sediments collected from a gravity sewer were cultivated in a laboratory reactor fed with real wastewater for more than one year to obtain intact sediments. Batch test results show significant sulfide production with an average rate of 9.20 ± 0.39 g S/m(2)·d from the sediments, which is significantly higher than the areal rate of sewer biofilms. In contrast, the average methane production rate is 1.56 ± 0.14 g CH4/m(2)·d at 20 °C, which is comparable to the areal rate of sewer biofilms. These results clearly show that the contributions of sewer sediments to sulfide and methane production cannot be ignored when evaluating sewer emissions. Microsensor and pore water measurements of sulfide, sulfate and methane in the sediments, microbial profiling along the depth of the sediments and mathematical modelling reveal that sulfide production takes place near the sediment surface due to the limited penetration of sulfate. In comparison, methane production occurs in a much deeper zone below the surface likely due to the better penetration of soluble organic carbon. Modelling results illustrate the dependency of sulfide and methane productions on the bulk sulfate and soluble organic carbon concentrations can be well described with half-order kinetics.

  17. Electroneutral intrinsic point defects in cadmium chalcogenides

    SciTech Connect

    Kharif, Ya.L.; Kudryashov, N.I.; Strunilina, T.A.

    1987-12-01

    Low-mobility electrically neutral intrinsic point defects were observed in cadmium chalcogenides. It was shown that the concentration of these defects is proportional to the cadmium vapor pressure to the 1/3 power at a constant temperature, and a mechanism for the formation of these defects were proposed.

  18. 29 CFR 1928.1027 - Cadmium.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 29 Labor 9 2011-07-01 2011-07-01 false Cadmium. 1928.1027 Section 1928.1027 Labor Regulations Relating to Labor (Continued) OCCUPATIONAL SAFETY AND HEALTH ADMINISTRATION, DEPARTMENT OF LABOR (CONTINUED) OCCUPATIONAL SAFETY AND HEALTH STANDARDS FOR AGRICULTURE Occupational Health § 1928.1027 Cadmium. See §...

  19. 29 CFR 1928.1027 - Cadmium.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 29 Labor 9 2013-07-01 2013-07-01 false Cadmium. 1928.1027 Section 1928.1027 Labor Regulations Relating to Labor (Continued) OCCUPATIONAL SAFETY AND HEALTH ADMINISTRATION, DEPARTMENT OF LABOR (CONTINUED) OCCUPATIONAL SAFETY AND HEALTH STANDARDS FOR AGRICULTURE Occupational Health § 1928.1027 Cadmium. See §...

  20. Effects of dietary cadmium on Mallard ducklings

    SciTech Connect

    Cain, B.W.; Sileo, L.; Franson, J.C.; Moore, J.

    1983-12-01

    Mallard (Anan platyrhynchos) ducklings were fed cadmium in the diet at 0, 5, 10, or 20 ppm from 1 day of age until 12 weeks of age. At 4-week intervals six males and six females from each dietary group were randomly selected, bled by jugular venipuncture, and necropsied. Significant decreases in packed cell volume (PCV) and hemoglobin (Hb) concentration and a significant increase in serum glutamic pyruvic transaminase (GPT) were found at 8 weeks of age in ducklings fed 20 ppm cadmium for 12 weeks. No other blood chemistry measurement, hematological parameter, or tissue histopathological measurement indicated a reaction to cadmium ingestion. Body weight, liver weight, and the ratio of the femur weight to length were not affected by dietary cadmium. Femur cadmium concentration in all ducklings 12 weeks of age declined from the values detected at 4 and 8 weeks of age. Liver cadmium concentrations were significantly higher in relation to the increased dietary levels and in relation to the length of time the ducklings were fed the cadmium diets. At 12 weeks of age the cadmium concentration in liver tissue was twice that in the diet. 38 references.

  1. Cadmium concentrations in tobacco and tobacco smoke

    SciTech Connect

    Scherer, G.; Barkemeyer, H.

    1983-02-01

    The amount of cadmium in tobacco depends on the variety and origin of the plant as well as on the analytical method used to determine cadmium. In the literature, cadmium concentrations in tobacco of between 0.5 and 5 ppm are reported. Modern German cigarette tobacco contains about 0.5-1.5 micrograms cadmium/cigarette. Of importance for the smoker is the amount of the metal in the mainstream smoke. The cadmium level in the mainstream smoke of modern cigarettes is reduced by means of filters and other construction features. The average Cd value of German filter cigarettes is less than 0.1 microgram/cigarette in mainstream smoke. An average daily intake of about 1 microgram cadmium by smoking 20 cigarettes can be calculated on the basis of an experimentally proved pulmonary retention rate of 50%. Pulmonary resorption rates relevant to uptake rates of cadmium by smoking are discussed. It can be assumed that cadmium uptake by smoking modern cigarettes has been reduced because of modifications in tobacco processing and cigarette construction in the last few decades.

  2. Association of urinary cadmium and myocardial infarction

    SciTech Connect

    Everett, Charles J. Frithsen, Ivar L.

    2008-02-15

    We conducted a cross-sectional analysis of individuals 45-79 years old in the National Health and Nutrition Examination Survey III (1988-1994) (NHANES III). Myocardial infarction was determined by electrocardiogram (ECG). Our sample included 4912 participants, which when weighted represented 52,234,055 Americans. We performed adjusted logistic regressions with the Framingham risk score, pack-years of smoking, race-ethnicity, and family history of heart attack, and diabetes as covariates. Urinary cadmium {>=}0.88 {mu}g/g creatinine had an odds ratio of 1.86 (95% CI 1.26-2.75) compared to urinary cadmium <0.43 {mu}g/g creatinine. This result supports the hypothesis that cadmium is associated with coronary heart disease. When logistic regressions were done by gender, women, but not men, showed a significant association of urinary cadmium with myocardial infarction. Women with urinary cadmium {>=}0.88 {mu}g/g creatinine had an odds ratio of 1.80 (95% CI 1.06-3.04) compared to urinary cadmium <0.43 {mu}g/g creatinine. When the analysis was restricted to never smokers (N=2187) urinary cadmium {>=}0.88 {mu}g/g creatinine had an odds ratio of 1.85 (95% CI 1.10-3.14) compared to urinary cadmium <0.43 {mu}g/g creatinine.

  3. 29 CFR 1915.1027 - Cadmium.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 29 Labor 7 2012-07-01 2012-07-01 false Cadmium. 1915.1027 Section 1915.1027 Labor Regulations Relating to Labor (Continued) OCCUPATIONAL SAFETY AND HEALTH ADMINISTRATION, DEPARTMENT OF LABOR (CONTINUED... Cadmium. Note: The requirements applicable to shipyard employment under this section are identical...

  4. 29 CFR 1915.1027 - Cadmium.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 29 Labor 7 2011-07-01 2011-07-01 false Cadmium. 1915.1027 Section 1915.1027 Labor Regulations Relating to Labor (Continued) OCCUPATIONAL SAFETY AND HEALTH ADMINISTRATION, DEPARTMENT OF LABOR (CONTINUED... Cadmium. Note: The requirements applicable to shipyard employment under this section are identical...

  5. 29 CFR 1915.1027 - Cadmium.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 29 Labor 7 2013-07-01 2013-07-01 false Cadmium. 1915.1027 Section 1915.1027 Labor Regulations Relating to Labor (Continued) OCCUPATIONAL SAFETY AND HEALTH ADMINISTRATION, DEPARTMENT OF LABOR (CONTINUED... Cadmium. Note: The requirements applicable to shipyard employment under this section are identical...

  6. 29 CFR 1915.1027 - Cadmium.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 29 Labor 7 2010-07-01 2010-07-01 false Cadmium. 1915.1027 Section 1915.1027 Labor Regulations Relating to Labor (Continued) OCCUPATIONAL SAFETY AND HEALTH ADMINISTRATION, DEPARTMENT OF LABOR (CONTINUED... Cadmium. Note: The requirements applicable to shipyard employment under this section are identical...

  7. 29 CFR 1915.1027 - Cadmium.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 29 Labor 7 2014-07-01 2014-07-01 false Cadmium. 1915.1027 Section 1915.1027 Labor Regulations Relating to Labor (Continued) OCCUPATIONAL SAFETY AND HEALTH ADMINISTRATION, DEPARTMENT OF LABOR (CONTINUED... Cadmium. Note: The requirements applicable to shipyard employment under this section are identical...

  8. Classification of polytype structures of zinc sulfide

    SciTech Connect

    Laptev, V.I.

    1994-12-31

    It is suggested that the existing classification of polytype structures of zinc sulfide be supplemented with an additional criterion: the characteristic of regular point systems (Wyckoff positions) including their type, number, and multiplicity. The consideration of the Wyckoff positions allowed the establishment of construction principles of known polytype series of different symmetries and the systematization (for the first time) of the polytypes with the same number of differently packed layers. the classification suggested for polytype structures of zinc sulfide is compact and provides a basis for creating search systems. The classification table obtained can also be used for numerous silicon carbide polytypes. 8 refs., 4 tabs.

  9. Modeling of Sulfide Microenvironments on Mars

    NASA Technical Reports Server (NTRS)

    Schwenzer, S. P.; Bridges, J. C.; McAdam, A.; Steer, E. D.; Conrad, P. G.; Kelley, S. P.; Wiens, R. C.; Mangold, N.; Grotzinger, J.; Eigenbrode, J. L.; Franz, H. B.; Sutter, B.

    2016-01-01

    Yellowknife Bay (YKB; sol 124-198) is the second site that the Mars Science Laboratory Rover Curiosity investigated in detail on its mission in Gale Crater. YKB represents lake bed sediments from an overall neutral pH, low salinity environment, with a mineralogical composition which includes Ca-sulfates, Fe oxide/hydroxides, Fe-sulfides, amorphous material, and trioctahedral phyllosilicates. We investigate whether sulfide alteration could be associated with ancient habitable microenvironments in the Gale mudstones. Some textural evidence for such alteration may be pre-sent in the nodules present in the mudstone.

  10. Acute inhalation toxicity of carbonyl sulfide

    SciTech Connect

    Benson, J.M.; Hahn, F.F.; Barr, E.B.

    1995-12-01

    Carbonyl sulfide (COS), a colorless gas, is a side product of industrial procedures sure as coal hydrogenation and gasification. It is structurally related to and is a metabolite of carbon disulfide. COS is metabolized in the body by carbonic anhydrase to hydrogen sulfide (H{sub 2}S), which is thought to be responsible for COS toxicity. No threshold limit value for COS has been established. Results of these studies indicate COS (with an LC{sub 50} of 590 ppm) is slightly less acutely toxic than H{sub 2}S (LC{sub 50} of 440 ppm).

  11. Aromatic sulfide/sulfone polymer production

    SciTech Connect

    Scoggins, L.E.; Hoover, K.C.; Shang, W.W.

    1991-05-14

    This patent describes a process for the production of aromatic sulfide/sulfone polymer. It comprises: contacting at least one lactam, at least one alkali metal hydrosulfide, water, and at least one base selected from the group consisting of alkali metal hydroxides and mixtures of alkali metal hydroxides with alkali metal carbonates under reaction conditions of time and temperature sufficient to produce a mixture containing a complex which comprises the at least one alkali metal hydrosulfide and contacting the mixture produced with a least one dihaloaromatic sulfone under polymerization conditions for a period of time sufficient to form an aromatic sulfide/sulfone polymer.

  12. Evolution of sulfide mineralization on Mars

    NASA Technical Reports Server (NTRS)

    Burns, Roger G.; Fisher, Duncan S.

    1990-01-01

    It has been previously suggested, on the basis of compositional and petrographic similarities noted between komatites, SNC meteorites, and the silicate portion of the Martian regolith fines, that iron-sulfide ore deposites may exist on Mars. This paper examines the possible locations of Archean-type sulfide and related ore deposits on Mars, their evolution, and the emplacement mechanisms for the ore deposit. The clues to these questions are deduced by applying to Mars the temporal patterns of ore distribution on earth and the experimental observations on sulfur solubility in basaltic melts.

  13. Membrane for hydrogen recovery from streams containing hydrogen sulfide

    DOEpatents

    Agarwal, Pradeep K.

    2007-01-16

    A membrane for hydrogen recovery from streams containing hydrogen sulfide is provided. The membrane comprises a substrate, a hydrogen permeable first membrane layer deposited on the substrate, and a second membrane layer deposited on the first layer. The second layer contains sulfides of transition metals and positioned on the on a feed side of the hydrogen sulfide stream. The present invention also includes a method for the direct decomposition of hydrogen sulfide to hydrogen and sulfur.

  14. Method for inhibiting oxidation of metal sulfide-containing material

    DOEpatents

    Elsetinow, Alicia; Borda, Michael J.; Schoonen, Martin A.; Strongin, Daniel R.

    2006-12-26

    The present invention provides means for inhibiting the oxidation of a metal sulfide-containing material, such as ore mine waste rock or metal sulfide taiulings, by coating the metal sulfide-containing material with an oxidation-inhibiting two-tail lipid coating (12) thereon, thereby inhibiting oxidation of the metal sulfide-containing material in acid mine drainage conditions. The lipids may be selected from phospholipids, sphingolipids, glycolipids and combinations thereof.

  15. Magnetic sulfide-modified nanoscale zerovalent iron (S-nZVI) for dissolved metal ion removal.

    PubMed

    Su, Yiming; Adeleye, Adeyemi S; Keller, Arturo A; Huang, Yuxiong; Dai, Chaomeng; Zhou, Xuefei; Zhang, Yalei

    2015-05-01

    Sulfide-modified nanoscale zerovalent iron (S-nZVI) is attracting a lot of attention due to its ease of production and high reactivity with organic pollutants. However, its structure is still poorly understood and its potential application in heavy metal remediation has not been explored. Herein, the structure of S-nZVI and its cadmium (Cd) removal performance under different aqueous conditions were carefully investigated. Transmission electron microscopy (TEM) with an energy-dispersive X-ray spectroscopy (EDS) analysis suggested that sulfur was incorporated into the zerovalent iron core. Scanning electron microscopy (SEM) with EDS analysis demonstrated that sulfur was also homogeneously distributed within the nanoparticles. When the concentration of Na2S2O4 was increased during synthesis, a flake-like structure (FeSx) increased significantly. S-nZVI had an optimal Cd removal capacity of 85 mg/g, which was >100% higher than for pristine nZVI. Even at pH 5, over 95% removal efficiency was observed, indicating sulfide compounds played a crucial role in metal ion removal and particle chemical stability. Oxygen impaired the structure of S-nZVI but enhanced Cd removal capacity to about 120 mg/g. Particle aging had no negative effect on removal capacity of S-nZVI, and Cd-containing mixtures remained stable in a two months experiment. S-nZVI can efficiently sequester dissolved metal ions from different contaminated water matrices. PMID:25706223

  16. Phase-selective cation-exchange chemistry in sulfide nanowire systems.

    PubMed

    Zhang, Dandan; Wong, Andrew B; Yu, Yi; Brittman, Sarah; Sun, Jianwei; Fu, Anthony; Beberwyck, Brandon; Alivisatos, A Paul; Yang, Peidong

    2014-12-17

    As a cation-deficient, p-type semiconductor, copper sulfide (Cu(2-x)S) shows promise for applications such as photovoltaics, memristors, and plasmonics. However, these applications demand precise tuning of the crystal phase as well as the stoichiometry of Cu(2-x)S, an ongoing challenge in the synthesis of Cu(2-x)S materials for a specific application. Here, a detailed transformation diagram of cation-exchange (CE) chemistry from cadmium sulfide (CdS) into Cu(2-x)S nanowires (NWs) is reported. By varying the reaction time and the reactants' concentration ratio, the progression of the CE process was captured, and tunable crystal phases of the Cu(2-x)S were achieved. It is proposed that the evolution of Cu(2-x)S phases in a NW system is dependent on both kinetic and thermodynamic factors. The reported data demonstrate that CE can be used to precisely control the structure, composition, and crystal phases of NWs, and such control may be generalized to other material systems for a variety of practical applications.

  17. Solar Mesosphere Explorer

    NASA Technical Reports Server (NTRS)

    1981-01-01

    Five experiments and the instruments packages designed for use in studying reactions between sunlight, ozone, and other chemicals in the atmosphere as well as for determining how ozone concentrations are transported in the mesosphere are described. The spin-stabilized satellite carrying the experiments consists of an observatory module and a spacecraft bus. Powered by a solar array which charges the nickel-cadmium batteries, the satellite is to be inserted into a sun synchronous orbit by a two stage Delta 2310 launch vehicle. The mission objectives, spacecraft configurations, and various subsystems are described as well as the ground support and prelaunch operations.

  18. Assessment of Hybrid Organic-Inorganic Antimony Sulfides for Earth-Abundant Photovoltaic Applications.

    PubMed

    Yang, Ruo Xi; Butler, Keith T; Walsh, Aron

    2015-12-17

    Hybrid organic-inorganic solar absorbers are currently the subject of intense interest; however, the highest-performing materials contain Pb. Here we assess the potential of three Sb-based semiconductors: (i) Sb2S3, (ii) Cs2Sb8S13, and (iii) (CH3NH3)2Sb8S13. While the crystal structure of Sb2S3 is composed of 1D chains, 2D layers are formed in the ternary cesium and hybrid methylammonium antimony sulfide compounds. In each case, a stereochemically active Sb 5s(2) lone pair is found, resulting in a distorted coordination environment for the Sb cations. The bandgap of the binary sulfide is found to increase, while the ionization potential also changes, upon transition to the more complex compounds. Based on the predicted electronic structure, device configurations are suggested to be suitable for photovoltaic applications. PMID:26624204

  19. Synthesis of 4H/fcc-Au@Metal Sulfide Core-Shell Nanoribbons.

    PubMed

    Fan, Zhanxi; Zhang, Xiao; Yang, Jian; Wu, Xue-Jun; Liu, Zhengdong; Huang, Wei; Zhang, Hua

    2015-09-01

    Although great advances on the synthesis of Au-semiconductor heteronanostructures have been achieved, the crystal structure of Au components is limited to the common face-centered cubic (fcc) phase. Herein, we report the synthesis of 4H/fcc-Au@Ag2S core-shell nanoribbon (NRB) heterostructures from the 4H/fcc Au@Ag NRBs via the sulfurization of Ag. Remarkably, the obtained 4H/fcc-Au@Ag2S NRBs can be further converted to a novel class of 4H/fcc-Au@metal sulfide core-shell NRB heterostructures, referred to as 4H/fcc-Au@MS (M = Cd, Pb or Zn), through the cation exchange. We believe that these novel 4H/fcc-Au@metal sulfide NRB heteronanostructures may show some promising applications in catalysis, surface enhanced Raman scattering, solar cells, photothermal therapy, etc.

  20. Assessment of Hybrid Organic-Inorganic Antimony Sulfides for Earth-Abundant Photovoltaic Applications.

    PubMed

    Yang, Ruo Xi; Butler, Keith T; Walsh, Aron

    2015-12-17

    Hybrid organic-inorganic solar absorbers are currently the subject of intense interest; however, the highest-performing materials contain Pb. Here we assess the potential of three Sb-based semiconductors: (i) Sb2S3, (ii) Cs2Sb8S13, and (iii) (CH3NH3)2Sb8S13. While the crystal structure of Sb2S3 is composed of 1D chains, 2D layers are formed in the ternary cesium and hybrid methylammonium antimony sulfide compounds. In each case, a stereochemically active Sb 5s(2) lone pair is found, resulting in a distorted coordination environment for the Sb cations. The bandgap of the binary sulfide is found to increase, while the ionization potential also changes, upon transition to the more complex compounds. Based on the predicted electronic structure, device configurations are suggested to be suitable for photovoltaic applications.