Effect of copper sulphate supplementation on performance of broiler chickens, cholesterol content and fatty acid profile of meat

Czech Academy of Sciences Publication Activity Database

Skřivan, M.; Ševčíková, S.; Tůmová, E.; Skřivanová, V.; Marounek, Milan

2002-01-01

Roč. 47, č. 7 (2002), s. 275-280 ISSN 1212-1819 R&D Projects: GA AV ČR KSK5020115 Grant - others:GA NATO(XX) MO2-99-04 Keywords : broiler * copper sulphate * quality of meat Subject RIV: GH - Livestock Nutrition Impact factor: 0.187, year: 2002

Copper Powder and Chemicals: edited proceedings of a seminar

Energy Technology Data Exchange (ETDEWEB)

1980-12-01

Various papers are presented covering the following topics: Status of Copper Chemical Industry in India, Copper Powder from Industrial Wastes, Manufacture of Copper Hydroxide and High Grade Cement Copper from Low Grade Copper Ore, Manufacture of Copper Sulphate as a By-Product, Hydrometallurgical Treatments of Copper Converter and Smelter Slage for Recovering Copper and other Non-Ferrous Metals, Recovery of Copper from Dilute Solutions, Use of Copper Compounds as Fungicides in India, Copper in Animal Husbandry, and Use of Copper Powder and Chemicals for Marine Applications. The keynote paper given at the Seminar was on Conservation of Copper for Better Use.

Hepatocyte nuclear structure and subcellular distribution of copper in zebrafish Brachydanio rerio and roach Rutilus rutilus (Teleostei, Cyprinidae) exposed to copper sulphate

Energy Technology Data Exchange (ETDEWEB)

Paris-Palacios, Severine [Universite de Reims Champagne-Ardenne (URCA), UFR Sciences Exactes et Naturelles, Laboratoire d' Eco-Toxicologie, Institut International de Recherche sur les Ions Metalliques, B.P. 1039-51687 Reims cedex 2 (France)]. E-mail: severine.paris@univ-reims.fr; Biagianti-Risbourg, Sylvie [Universite de Reims Champagne-Ardenne (URCA), UFR Sciences Exactes et Naturelles, Laboratoire d' Eco-Toxicologie, Institut International de Recherche sur les Ions Metalliques, B.P. 1039-51687 Reims cedex 2 (France)]. E-mail: sylvie.biagianti@univ-reims.fr

2006-05-10

Copper is a trace element essential to life, but also a heavy metal with toxic effect clearly demonstrated. Cu induced perturbations in fish liver are well documented but the variability of the reported results is large. In this study two cyprinids, zebrafish and roach, were exposed to copper. Reported histocytological changes are either adaptative or degenerative depending on fish species, concentration of metal, and duration of exposure. Hepatic subcellular distribution of copper was determined by X-ray microanalysis in control and Cu-exposed roach and zebrafish. Sublethal copper sulphate contamination induced the development of a particular nucleolar alteration forming a network or honeycomb like structure in liver. This perturbation is observable in almost all the hepatocytes of zebrafish and roach exposed to copper for a minimum of 4 days of exposure. It seemed to concern more precisely the pars fibrosa. X-ray microanalysis showed that the appearance of network nucleolus was in relation to a Cu accumulation. Cu deposit was well located in the network as pars granulosa and nucloplasm showed very lower metal concentrations. The origin and consequence of network structure in nucleolus was discussed.

Hepatocyte nuclear structure and subcellular distribution of copper in zebrafish Brachydanio rerio and roach Rutilus rutilus (Teleostei, Cyprinidae) exposed to copper sulphate

International Nuclear Information System (INIS)

Paris-Palacios, Severine; Biagianti-Risbourg, Sylvie

2006-01-01

Copper is a trace element essential to life, but also a heavy metal with toxic effect clearly demonstrated. Cu induced perturbations in fish liver are well documented but the variability of the reported results is large. In this study two cyprinids, zebrafish and roach, were exposed to copper. Reported histocytological changes are either adaptative or degenerative depending on fish species, concentration of metal, and duration of exposure. Hepatic subcellular distribution of copper was determined by X-ray microanalysis in control and Cu-exposed roach and zebrafish. Sublethal copper sulphate contamination induced the development of a particular nucleolar alteration forming a network or honeycomb like structure in liver. This perturbation is observable in almost all the hepatocytes of zebrafish and roach exposed to copper for a minimum of 4 days of exposure. It seemed to concern more precisely the pars fibrosa. X-ray microanalysis showed that the appearance of network nucleolus was in relation to a Cu accumulation. Cu deposit was well located in the network as pars granulosa and nucloplasm showed very lower metal concentrations. The origin and consequence of network structure in nucleolus was discussed

Copper sulphate use in South African traditional medicine.

Science.gov (United States)

Street, Renée A; Kabera, Gaëtan M; Connolly, Catherine

2017-06-01

Copper (Cu) is an essential element to humans; however, exposure to elevated concentrations through occupational hazard and/or environmental means may be detrimental. This paper provides results of a cross-sectional study aimed to determine the prevalence of copper sulphate (CuSO 4 ) use in South African traditional medicine by traditional health practitioners (THPs) and details the use thereof. A total of 201 THPs were enrolled from two main municipal areas of KwaZulu-Natal (South Africa). Information on demographic characteristics of THPs, reasons for using or not using CuSO 4 as well as administration methods and age groups of recipients were collected. Of the 201 THPs interviewed, 145 (72 %) use CuSO 4 for healing purposes. The use of CuSO 4 was strongly associated with gender (p = 0.009) where the proportion of CuSO 4 users was higher for female than male THPs. CuSO 4 was reportedly administered to individuals of all ages, including infants and children. The main routes of administration were enema (n = 110; 76 %), oral (n = 40; 28 %) and use in bath (n = 40; 28 %). The reasons cited for use are diverse and included skin rashes (n = 43; 30 %), aches, pains and swelling (n = 38; 28 %) as well as sexually transmitted diseases (n = 28; 19 %). This study identified a high prevalence of THPs using CuSO 4 for healing purposes. These findings support the need to regulate South African traditional medicine to safeguard the user.

[Leaching of nonferrous metals from copper-smelting slag with acidophilic microorganisms].

Science.gov (United States)

Murav'ev, M I; Fomchenko, N V

2013-01-01

The leaching process of copper and zinc from copper converter slag with sulphuric solutions of trivalent iron sulphate obtained using the association of acidophilic chemolithotrophic microorganisms was investigated. The best parameters of chemical leaching (temperature 70 degrees C, an initial concentration of trivalent iron in the leaching solution of 10.1 g/L, and a solid-phase content in the suspension of 10%) were selected. Carrying out the process under these parameters resulted in the recovery of 89.4% of copper and 39.3% of zinc in the solution. The possibility of the bioregeneration of trivalent iron in the solution obtained after the chemical leaching of slag by iron-oxidizingacidophilic chemolithotrophic microorganisms without inhibiting their activity was demonstrated.

Alternative method of portable irradiation of manganese sulphate solution by an plutonium-beryllium source for manganese sulphate bath efficiency measurements

International Nuclear Information System (INIS)

Silva, Fellipe Souza da; Martins, Marcelo Marques; Pereira, Walsan Wagner

2016-01-01

This study intends to create an alternative irradiation system from a Plutonium-Beryllium source for manganese sulphate solution using the Monte Carlo code. Thus seeking to eliminate the issue of institutes that do not have reactors or particle accelerators in its infrastructure, in order to optimize and provide independence for them to carry out efficiency measurements of MnSO_4 solution in their own locality. The Monte Carlo simulations defined the technical features of this new system so that the solution reaches the maximum neutron capture by manganese in solution. (author)

Structure transitions between copper-sulphate and copper-chloride ...

Indian Academy of Sciences (India)

Administrator

strate that co-adsorbed sulphate ions in the (√3 × √3)R30° UPD adlayer are replaced by chloride ions and, ..... phase 1 by the (5 × 5)-like chlo- ride phase 2 was mentioned in. 45,46,48,56 but not stud- ied in detail. These authors suggested that the replacement of SO. 2. 4. – .... A nonlinear regression fit of (1) to the experi-.

The effect of surfactants on the electropolishing behavior of copper in orthophosphoric acid

Energy Technology Data Exchange (ETDEWEB)

Taha, A.A., E-mail: asia_taha@yahoo.com; Ahmed, A.M.; Rahman, H.H. Abdel; Abouzeid, F.M.

2013-07-15

The electropolishing behavior of copper was studied in orthophosphoric acid with Triton X-100, sodium dodecyl sulphate and cetyl pyridinium chloride as additives for improving the finish obtained on copper surface. This was investigated by measuring and comparing anode potential-limiting current relationships in solutions of gradually increasing concentration of surfactants. The addition of surfactants to the electropolishing solution results in a lower limiting current. This confirms the mass transport of dissolved species from the anode surface to the bulk of solution as the rate-determining step in the presence of three surfactants in all concentrations investigated. Scanning electron microscope (SEM), atomic force microscope (AFM) and measured brightness values were used to investigate the copper surface after electropolishing and the results were compared to polishing done in absence of surfactants. According to SEM images and brightness values, addition of Triton X-100 was effective to enhance levelling and brightening more than sodium dodecyl sulphate and cetyl pyridinium chloride. AFM analysis showed that the roughness values (R{sub a}) for an electropolished copper surface, in presence of surfactants, is significantly lower than in absence of surfactants. Different reaction conditions and the physical properties of solutions are studied to obtain dimensionless correlation among all these parameters.

[Biohydrometallurgical technology of a complex copper concentrate process].

Science.gov (United States)

Murav'ev, M I; Fomchenko, N V; Kondrat'eva, T F

2011-01-01

Leaching of sulfide-oxidized copper concentrate of the Udokan deposit ore with a copper content of 37.4% was studied. In the course of treatment in a sulfuric acid solution with pH 1.2, a copper leaching rate was 6.9 g/kg h for 22 h, which allowed extraction of 40.6% of copper. As a result of subsequent chemical leaching at 80 degrees C during 7 h with a solution of sulphate ferric iron obtained after bio-oxidation by an association of microorganisms, the rate of copper recovery was 52.7 g/kg h. The total copper recovery was 94.5% (over 29 h). Regeneration of the Fe3+ ions was carried out by an association of moderately thermophilic microorganisms, including bacteria of genus Sulfobacillus and archaea of genus Ferroplasma acidiphilum, at 1.0 g/l h at 40 degrees C in the presence of 3% solids obtained by chemical leaching of copper concentrate. A technological scheme of a complex copper concentrate process with the use of bacterial-chemical leaching is proposed.

Solution-processed copper-nickel nanowire anodes for organic solar cells

Science.gov (United States)

Stewart, Ian E.; Rathmell, Aaron R.; Yan, Liang; Ye, Shengrong; Flowers, Patrick F.; You, Wei; Wiley, Benjamin J.

2014-05-01

This work describes a process to make anodes for organic solar cells from copper-nickel nanowires with solution-phase processing. Copper nanowire films were coated from solution onto glass and made conductive by dipping them in acetic acid. Acetic acid removes the passivating oxide from the surface of copper nanowires, thereby reducing the contact resistance between nanowires to nearly the same extent as hydrogen annealing. Films of copper nanowires were made as oxidation resistant as silver nanowires under dry and humid conditions by dipping them in an electroless nickel plating solution. Organic solar cells utilizing these completely solution-processed copper-nickel nanowire films exhibited efficiencies of 4.9%.This work describes a process to make anodes for organic solar cells from copper-nickel nanowires with solution-phase processing. Copper nanowire films were coated from solution onto glass and made conductive by dipping them in acetic acid. Acetic acid removes the passivating oxide from the surface of copper nanowires, thereby reducing the contact resistance between nanowires to nearly the same extent as hydrogen annealing. Films of copper nanowires were made as oxidation resistant as silver nanowires under dry and humid conditions by dipping them in an electroless nickel plating solution. Organic solar cells utilizing these completely solution-processed copper-nickel nanowire films exhibited efficiencies of 4.9%. Electronic supplementary information (ESI) available. See DOI: 10.1039/c4nr01024h

Thermodynamic analysis of dust sulphation reactions

Energy Technology Data Exchange (ETDEWEB)

Yang Yongxiang; Jokilaakso, A.

1997-12-31

Sulphation reactions of metal oxides with SO{sub 2} and O. or SO{sub 3} play significant roles in sulphation roasting of sulphide and oxide minerals as well as in desulphurisation process of combustion gases. In metallurgical waste-heat boilers for sulphide smelting, the sulphation of the oxidic flue dust in the atmosphere containing sulphur oxides is an unavoidable process, and the sulphation reactions have to be guided in a controlled way in the proper parts of the gas handling equipment. In this report, some thermodynamic analyses were conducted for the oxide sulphation reactions in relation to sulphide smelting processes. The phase stability of Me-S-O systems especially for oxides - sulphates equilibrium was studied under different thermodynamic conditions of gas compositions and temperatures. The sulphate stability was analysed for an example of gas compositions in the copper flash smelter of Outokumpu Harjavalta Metals Oy, in relation to temperature. In the report, most of the information was from literature. Moreover, a number of thermodynamic computations were carried out with the HSC program, and the constructed phase stability diagrams were compared with those from the literature whenever possible. The maximum temperatures for stable sulphates under normal operating conditions of the waste-heat boilers in sulphide smelting processes were obtained. This report will serve as the basis for the kinetic studies of the sulphation reactions and the sulphation reaction modelling in pyrometallurgical processes. (orig.) SULA 2 Programme. 36 refs.

Sodium diethyldithiocarbamate as accelerator of the rate of copper cementation

Directory of Open Access Journals (Sweden)

Abeer A. El-Saharty

2015-12-01

Full Text Available The effects of Cu2+ ion concentration and temperature on the cementation rate of copper from copper sulphate on zinc and the effect of additives of the organic compound “sodium diethyldithiocarbamate” (NaDDC were studied. It was noticed that the cementation increases significantly by increasing the concentrations of NaDDC. The rate of cementation increased by 58.58−100.31%. Our data showed that sodium diethyldithiocarbamate reacts with the Cu2+ solution giving a complex of copper diethyldithiocarbamate, which enhances the rate of cementation.

Uranium and sulphate values from carbonate leach process

International Nuclear Information System (INIS)

Berger, B.

1983-01-01

The process concerns the recovery of uraniferous and sulphur values from liquor resulting from the attack of sulphur containing uraniferous ores by an alkaline solution of sodium carbonate and/or bicarbonate. Ammonia is introduced into the liquor to convert any HCO 3 - to CO 3 2- . The neutralised liquor from this step is then contacted with an anion exchange resin to fix the uranium and sulphate ions, leaving a liquor containing ammonia, sodium carbonate and/or bicarbonate in solution. Uranium and sulphate ions are eluted with an ammonia carbonate and/or bicarbonate solution to yield a solution of ammonium uranyl carbonate complex and ammonium sulphate. The solution is subjected to thermal treatment until a suspension of precipitated ammonium uranate and/or diuranate is obtained in a solution of the ammonium sulphate. Carbon dioxide, ammonia and water vapor are driven off. The precipitated ammonium uranate and/or diuranate is then separated from the solution of ammonium sulphate and the precipitate is calcined to yield uranium trioxide and ammonia

Microstructural characterization and electrochemical corrosion behavior of Incoloy 800 in sulphate and chloride solutions

International Nuclear Information System (INIS)

Mansur, Fabio Abud; Schvartzman, Monica Maria de Abreu Mendonca; Campos, Wagner Reis da Costa; Aguiar, Antonio Eugenio de; Chaim, Marcos Souza

2011-01-01

Corrosion has been the major cause of tube failures in steam generators (SG) tubes in nuclear power plants. Problems have resulted from impurities in the secondary water systems which are originated from leaks of cooling water. It is important to understand the compatibility of steam generator tube materials with the environment. This study presents the microstructural characterization and electrochemical behavior of the Incoloy 800 in sodium chloride and sodium sulphate aqueous solutions at 80 degree C. Potentiodynamic anodic polarization, cyclic polarization and open circuit potential (OCP) measurements were the electrochemical techniques applied in this work. The pitting resistance of Incoloy 800 in chloride plus sulphate mixtures were also examined. Experiments performed in solutions with different concentrations of Cl- and SO 4 2- ions in solution (200 ppb, 500 ppb, 1ppm, 5 ppm, 50 ppm and 100 ppm) showed that this concentrations range had no substantial effect on the anodic behavior of the alloy. After polarization no localized corrosion was found on the samples. (author)

Determination of semi-empirical relationship between the manganese and hydrogen atoms ratio, physical density and concentration in an aqueous solution of manganese sulphate

Energy Technology Data Exchange (ETDEWEB)

Rodrigues Bittencourt, Guilherme, E-mail: bittencourt@ird.gov.b [Instituto de Radioprotecao e Dosimetria LNMRI/IRD/CNEN, Av. Salvador Allende, s/n Recreio dos Bandeirantes, CEP 22780-160, Rio de Janeiro, RJ (Brazil); Souza Patrao, Karla Cristina de, E-mail: karla@ird.gov.b [Instituto de Radioprotecao e Dosimetria LNMRI/IRD/CNEN, Av. Salvador Allende, s/n Recreio dos Bandeirantes, CEP 22780-160, Rio de Janeiro, RJ (Brazil); Passos Leite, Sandro, E-mail: sandro@ird.gov.b [Programa de Engenharia Nuclear/COPPE, Universidade Federal do Rio de Janeiro, Ilha do Fundao, Caixa Postal 68509, 21945-970, Rio de Janeiro, RJ (Brazil); Wagner Pereira, Walsan, E-mail: walsan@ird.gov.b [Instituto de Radioprotecao e Dosimetria LNMRI/IRD/CNEN, Av. Salvador Allende, s/n Recreio dos Bandeirantes, CEP 22780-160, Rio de Janeiro, RJ (Brazil); Simoes da Fonseca, Evaldo, E-mail: evaldo@ird.gov.b [Instituto de Radioprotecao e Dosimetria LNMRI/IRD/CNEN, Av. Salvador Allende, s/n Recreio dos Bandeirantes, CEP 22780-160, Rio de Janeiro, RJ (Brazil)

2010-12-15

The Manganese sulphate solution has been used for neutron metrology through the method of Manganese Bath. This method uses physical parameters of manganese sulphate solution to obtain its corrections. This work established a functional relationship, using the gravimetric method, between those physical parameters: density, concentration and hydrogen to manganese ratio. Comparisons were done between manganese sulphate solution concentration from the Manganese Bath system of Laboratory of Metrology of Ionising Radiation and estimated values from the functional relationship obtained, showing percentage difference of less than 0.1%. This result demonstrates the usefulness in the correlation of the physical values of the solution to the MB.

Coprecipitation of cadmium with copper 8-hydroxyquinolate from homogeneous solution

International Nuclear Information System (INIS)

Takiyama, Kazuyoshi; Kozen, Terumi; Ueki, Yasuyo; Ishida, Hiromi

1976-01-01

The coprecipitation of copper and cadmium 8-hydroxyquinolates from homogeneous solution was conducted from the viewpoint of crystal and analytical chemistry. To the mixed solution containing copper and cadmium ions an 8-acetoxyquinoline solution was added by keeping the pH of the solution at 9 and the resulted solution was stirred at 25 0 C. The precipitate formed at each stage of the reaction was analyzed. The precipitates in an initial stage were composed of needle crystals which characterizes copper 8-hydroxyquinolate, and were associated with a slight amount of cadmium. The first half of the coprecipitation curve for the needle crystal formation resembles the logarithmic distribution curve of lambda equal to about 0.01. The precipitation of most of the copper ions was followed by the precipitation of cadmium 8-hydroxyquinolate crystal in the plate form. The needle crystals of copper 8-hydroxyquinolate started to dissolve and transformed to plate crystals. In the second half of the coprecipitation, both crystals, owing to the identical crystal structure, precipitated simultaneously and form a solid solution. When cadmium 8-hydroxyquinolate was precipitated by the PFHS method (precipitation from homogeneous solution) in the presence of the needle crystals of copper 8-hydroxyquinolate, the above mentioned phenomenon was observed. The precipitation of cadmium 8-hydroxyquinolate in the plate form is due to the seeding effect of the plate crystals of copper 8-hydroxyquinolate, which were scantily transformed from the needle crystals. The plate crystals of cadmium compound acts as a seed to transform the needle crystals of copper compound to plate crystals. (auth.)

21 CFR 864.9320 - Copper sulfate solution for specific gravity determinations.

Science.gov (United States)

2010-04-01

... 21 Food and Drugs 8 2010-04-01 2010-04-01 false Copper sulfate solution for specific gravity... Establishments That Manufacture Blood and Blood Products § 864.9320 Copper sulfate solution for specific gravity determinations. (a) Identification. A copper sulfate solution for specific gravity determinations is a device...

Adsorption of some heavy metals on sulphate and phosphate modified kaolinite clay

International Nuclear Information System (INIS)

Adebowale, K.O.; Unuabonah, I.E.; Olu-Owolabi, B.I.

2003-12-01

Kaolinite clay, in bright white lumps collected from from Ubulu-Ukwu, Delta State, Nigeria, was modified with 200μ.ml -1 of phosphate and sulphate anion and thereafter used to adsorb some heavy metals viz. lead (Pb), Cadmium (Cd), Zinc (Zn) and Copper (Cu) from aqueous solution of the metals. The metal ions showed the greatest affinity for the P-modified (P-mod) sorbents. The order of adsorption of P-mod follows the order: P-mod Pb > P-mod Cu > P-mod Zn > P-mod Cd . Desorption studies showed that the P-modified sorbents exhibited a very strong ability to specifically adsorb lead, copper and zinc and are therefore poorly desorbed. All the metals were easily desorbed from the unmodified sorbent. The potential of the modified sorbents are enumerated. (author)

Removal of Pb (II from Aqueous Solutions Using Mixtures of Bamboo Biochar and Calcium Sulphate, and Hydroxyapatite and Calcium Sulphate

Directory of Open Access Journals (Sweden)

Ahmed Hassan

2016-01-01

Full Text Available Sorption characteristics of Pb(II from aqueous solutions through a low-cost adsorbent mixture comprising of Bamboo biochar (BB and Calcium Sulphate (CS, and a more expensive mixture of Hydroxyapatite (HAP and Calcium Sulphate (CS, were investigated. The effects of equilibrium contact time, and adsorbate concentration conducted in batch experiments were studied. Adsorption equilibrium was established in 40 (min. The adsorption mechanism of Pb(II from these two adsorbent mixtures was carried out through a kinetic rate order. A pseudo second-order kinetic model was applied for the adsorption processes. The model yielded good correlation (R2 >0.999 of the experimental data. Adsorption of Pb(II using (BB&CS and (HAP&CS correlated well (R2 >0.99 with both the Langmuir and Freundlich isotherm equations under the concentration range studied. Hence, the effectiveness of an inexpensive natural material (BB&CS mixture in Pb(II removal is established, and is promising for use in other heavy metal adsorptions.

Copper electrodeposition from an acidic plating bath containing accelerating and inhibiting organic additives

International Nuclear Information System (INIS)

Pasquale, M.A.; Gassa, L.M.; Arvia, A.J.

2008-01-01

Copper electrodeposition on copper from still plating solutions of different compositions was investigated utilising electrochemical impedance spectroscopy (EIS), cyclic voltammetry, and scanning electron microscopy (SEM). An acid copper sulphate plating base solution was employed either with or without sodium chloride in the presence of a single additive, either polyethylene glycol (PEG) or 3-mercapto-2-propanesulphonic acid (MPSA), and their mixture. Thallium underpotential deposition/anodic stripping was employed to determine the adsorption capability of additives on copper. In the absence of chloride ions, MPSA shows a moderate adsorption on copper, whereas PEG is slightly adsorbed. At low cathodic overpotentials, the simultaneous presence of MPSA and chloride ions accelerates copper electrodeposition through the formation of an MPSA-chloride ion complex in the solution, particularly for about 220 μM sodium chloride. The reverse effect occurs in PEG-sodium chloride plating solutions. In this case, from EIS data the formation of a film that interferes with copper electrodeposition can be inferred. At higher cathodic overpotentials, when copper electrodeposition is under mass transport control, the cathode coverage by a PEG-copper chloride-mediated film becomes either partially or completely detached as the concentration of chloride ions at the negatively charged copper surface diminishes. The copper cathode grain topography at the μm scale depends on the cathodic overpotential, plating solution composition and average current density. Available data about the solution constituents and their adsorption on copper make it possible to propose a likely complex mechanism to understand copper electrodeposition from these media, including the accelerating effect of MPSA and the dynamics of PEG-copper chloride complex adsorbate interfering with the surface mobility of depositing copper ad-ions/ad-atoms

Growth of single crystals from solutions using semi-permeable membranes

Science.gov (United States)

Varkey, A. J.; Okeke, C. E.

1983-05-01

A technique suitable for growth of single crystals from solutions using semi-preamble membranes is described. Using this technique single crystals of copper sulphate, potassium bromide and ammonium dihydrogen phosphate have been successfully grown. Advantages of this technique over other methods are discussed.

Searching for the Optimal Sampling Solution: Variation in Invertebrate Communities, Sample Condition and DNA Quality.

Directory of Open Access Journals (Sweden)

Martin M Gossner

Full Text Available There is a great demand for standardising biodiversity assessments in order to allow optimal comparison across research groups. For invertebrates, pitfall or flight-interception traps are commonly used, but sampling solution differs widely between studies, which could influence the communities collected and affect sample processing (morphological or genetic. We assessed arthropod communities with flight-interception traps using three commonly used sampling solutions across two forest types and two vertical strata. We first considered the effect of sampling solution and its interaction with forest type, vertical stratum, and position of sampling jar at the trap on sample condition and community composition. We found that samples collected in copper sulphate were more mouldy and fragmented relative to other solutions which might impair morphological identification, but condition depended on forest type, trap type and the position of the jar. Community composition, based on order-level identification, did not differ across sampling solutions and only varied with forest type and vertical stratum. Species richness and species-level community composition, however, differed greatly among sampling solutions. Renner solution was highly attractant for beetles and repellent for true bugs. Secondly, we tested whether sampling solution affects subsequent molecular analyses and found that DNA barcoding success was species-specific. Samples from copper sulphate produced the fewest successful DNA sequences for genetic identification, and since DNA yield or quality was not particularly reduced in these samples additional interactions between the solution and DNA must also be occurring. Our results show that the choice of sampling solution should be an important consideration in biodiversity studies. Due to the potential bias towards or against certain species by Ethanol-containing sampling solution we suggest ethylene glycol as a suitable sampling solution when

A Study on the Copper Effect on gold leaching in copper-ethanediamine-thiosulphate solutions

Science.gov (United States)

Liu, Qiong; Xiang, Pengzhi; Huang, Yao

2018-01-01

A simple, fast and sensitive square-wave voltammetry (SWV), cyclic voltammetry(CV) and tafel method for the determination of various factors of gold in thiosulphate solution in this paper. We present our study on the effect of copper(II) on the leaching of gold in thiosulphate solutions. The current study aims to establish the interaction of copper in the leaching process by electrochemical method.

Quenching characteristics of bathocuproinedisulfonic acid, disodium salt in aqueous solution and copper sulfate plating solution

Science.gov (United States)

Koga, Toshiaki; Hirakawa, Chieko; Takeshita, Michinori; Terasaki, Nao

2018-04-01

Bathocuproinedisulfonic acid, disodium salt (BCS) is generally used to detect Cu(I) through a color reaction. We newly found BCS fluorescence in the visible blue region in an aqueous solution. However, the fluorescence mechanism of BCS is not well known, so we should investigate its fundamental information. We confirmed that the characteristics of fluorescence are highly dependent on the molecular concentration and solvent properties. In particular, owing to the presence of the copper compound, the fluorescence intensity extremely decreases. By fluorescence quenching, we observed that a copper compound concentration of 10-6 mol/L or less could easily be measured in an aqueous solution. We also observed BCS fluorescence in copper sulfate plating solution and the possibility of detecting monovalent copper by fluorescence reabsorption.

solution growth and characterization of copper oxide thin films ...

African Journals Online (AJOL)

Thin films of copper oxide (CuO) were grown on glass slides by using the solution growth technique. Copper cloride (CuCl ) and potassium telluride (K T O ) were used. Buffer 2 2e 3 solution was used as complexing agent. The solid state properties and optical properties were obtained from characterization done using PYE ...

Physicochemical and in vitro deposition properties of salbutamol sulphate/ipratropium bromide and salbutamol sulphate/excipient spray dried mixtures for use in dry powder inhalers.

Science.gov (United States)

Corrigan, Deirdre O; Corrigan, Owen I; Healy, Anne Marie

2006-09-28

The physicochemical and aerodynamic properties of spray dried powders of the drug/drug mixture salbutamol sulphate/ipratropium bromide were investigated. The in vitro deposition properties of spray dried salbutamol sulphate and the spray dried drug/excipient mixtures salbutamol sulphate/lactose and salbutamol sulphate/PEG were also determined. Spray drying ipratropium bromide monohydrate resulted in a crystalline material from both aqueous and ethanolic solution. The product spray dried from aqueous solution consisted mainly of ipratropium bromide anhydrous. There was evidence of the presence of another polymorphic form of ipratropium bromide. When spray dried from ethanolic solution the physicochemical characterisation suggested the presence of an ipratropium bromide solvate with some anhydrous ipratropium bromide. Co-spray drying salbutamol sulphate with ipratropium bromide resulted in amorphous composites, regardless of solvent used. Particles were spherical and of a size suitable for inhalation. Twin impinger studies showed an increase in the fine particle fraction (FPF) of spray dried salbutamol sulphate compared to micronised salbutamol sulphate. Co-spray dried salbutamol sulphate:ipratropium bromide 10:1 and 5:1 systems also showed an increase in FPF compared to micronised salbutamol sulphate. Most co-spray dried salbutamol sulphate/excipient systems investigated demonstrated FPFs greater than that of micronised drug alone. The exceptions to this were systems containing PEG 4000 20% or PEG 20,000 40% both of which had FPFs not significantly different from micronised salbutamol sulphate. These two systems were crystalline unlike most of the other spray dried composites examined which were amorphous in nature.

Adsorption of 2-mercaptobenzothiazole on copper surface from phosphate solutions

International Nuclear Information System (INIS)

Kazansky, L.P.; Selyaninov, I.A.; Kuznetsov, Yu.I.

2012-01-01

Analysis of the electrochemical and XPS results has shown that adsorption of 2-mercaptobenzothiazole (MBT) on copper electrodes in neutral phosphate solutions proceeds through the formation of the chemical bonds by copper (I) cations with exo-sulfur and nitrogen atoms. A protection layer formed of Cu(I)MBT complex prevents precipitation of copper (II) phosphate on a copper surface. The thickness of the surface film consisting of a complex [Cu(I)MBT] n (having probably polymeric nature), where MBT acts as at least three-dentate ligand, increases depending on the exposure time, reaching 8-9 nm after immersing for 12 h in test solution. Even in a case of the preliminary formation of copper (II) phosphate on the copper electrode at the anodic potential addition of small amounts of MBT results in complete removal of copper (II) phosphate from the surface.

Study of fatigue crack nucleation in 12% chromium stainless steel in sulphate and phosphate solutions

International Nuclear Information System (INIS)

Shalaby, H.M.; Begley, J.A.; Macdonald, D.D.

1989-01-01

The morphology of fatigue crack nucleation has been studied in 12%Cr stainless steel at a single stress level of 448 MN m -2 in deaerated H 2 SO 4 -Na 2 SO 4 -NaOH ([SO 4 2- ] = 0.01M and 1M) and in H 3 PO 4 -NaOH ([PO 4 3- ] = 0.01M and 1M) solutions at pH 2, 7 and 10 at 100 0 C. In sulphate solutions at pH 2, the specimen suffered overall surface attack without the initiation of microcracks. The surface attack intensified at the prior austenite grain boundaries, martensite platelet boundaries, and non-metallic inclusions. In contrast, cracks initiated transgranularly in sulphate solutions at pH 7 and 10 with the development of selective attack at crack sites at later stages in the fatigue life. This attack was ascribed to local acidification as a result of hydrolysis of corrosion products extruded from inside the cracks. Long cracks with crack branching and debonded zones were observed in all phosphate solutions, except in 0.01M phosphate solution at pH 7. In this latter environment, short intrusion-extrusion microcracks were observed. This difference in behaviour was attributed to changes in the characteristics of the passive film as influenced by the local environmental conditions, mechanical rupture by plastic deformation, and electrochemical differences at the metal surface. (author)

A novel compound cleaning solution for benzotriazole removal after copper CMP

International Nuclear Information System (INIS)

Gu Zhangbing; Liu Yuling; Gao Baohong; Wang Chenwei; Deng Haiwen

2015-01-01

After the chemical mechanical planarization (CMP) process, the copper surface is contaminated by a mass of particles (e.g. silica) and organic residues (e.g. benzotriazole), which could do great harm to the integrated circuit, so post-CMP cleaning is essential. In particular, benzotriazole (BTA) forms a layer of Cu-BTA film with copper on the surface, which leads to a hydrophobic surface of copper. So an effective cleaning solution is needed to remove BTA from the copper surface. In this work, a new compound cleaning solution is designed to solve two major problems caused by BTA: one is removing BTA and the other is copper surface corrosion that is caused by the cleaning solution. The cleaning solution is formed of alkaline chelating agent (FA/O II type), which is used to remove BTA, and a surfactant (FA/O I type), which is used as a corrosion inhibitor. BTA removal is characterized by contact angle measurements and electrochemical techniques. The inhibiting corrosion ability of the surfactant is also characterized by electrochemical techniques. The proposed compound cleaning solution shows advantages in removing BTA without corroding the copper surface. (paper)

Polypyrrole electrodeposited on copper from an aqueous phosphate solution: Corrosion protection properties

OpenAIRE

Redondo, Clara; Breslin, Carmel B.

2007-01-01

Highly adherent and homogenous polypyrrole films were electrodeposited at copper from a dihydrogen phosphate solution. The polypyrrole films were electrosynthesized in the overoxidized state by cycling the copper electrode from –0.4 to 1.8 V (SCE) in a pyrrole-containing phosphate solution. The growth of the polypyrrole films was facilitated by the initial oxidation of the copper electrode in the phosphate solution to generate a mixed copper–phosphate, copper oxide or hydroxide layer. This la...

Preparation and characterization of composites of ultrasonic gel and copper sulphate for using as magnetic resonance body simulator; Preparação e caracterização de compósitos de gel de ultrassom e sulfato de cobre para uso como simulador de corpo em exames de resonância magnética

Energy Technology Data Exchange (ETDEWEB)

Cardoso, Gabriela P.; Soares, Sidney S.; Gontijo, Rodrigo M.G.; Batista, Adriana S.M., E-mail: sidneyss70soares@gmail.com, E-mail: gabrielapontesc@gmail.com, E-mail: rodrigogadelhagontijo1@hotmail.com, E-mail: driananuclear@yahoo.com.br [Universidade Federal de Minas Gerais (UFMG), Belo Horizonte, MG (Brazil). Departamento de Anatomia e Imagem; Pereira, Esther Lorrayne M., E-mail: esther_machado@outlook.com.br [Universidade Federal de Minas Gerais (UFMG), Belo Horizonte, MG (Brazil). Departamento de Engenharia Nuclear

2017-07-01

The use of magnetic resonance (MRI) body simulators has application in both equipment control and didactics, providing training to new professionals, regarding the manipulation of parameters related to image weights. For this, it is necessary to simulate longitudinal (T1) and transverse (T2) relaxation times in order to control the extrinsic echo time (TE) and repetition time (TR) parameters in obtaining images with different contrasts. For this purpose, composites with different proportions of ultrasonic gel and copper sulphate were prepared for submission to MRI for the characterization of the times T1 and T2. The selection of copper sulphate, paramagnetic material, was conducted considering relaxation times similar to the different body tissues in order to reproduce images of suitable contrasts. Copper sulphate powder was characterized by the X-Ray Diffraction (XRD) technique which showed characteristic peaks of copper and sulfate group. The composite was evaluated using Fourier Transform Infrared Spectrometry (FTIR) and Visible Ultraviolet Spectrometry (UV-Vis) techniques, demonstrating composite stability for future imaging tests. In the UV-Vis analyzes the peak centered at 725 nm was monitored by the overlap of the peaks at wavelengths between 200 - 450 nm, gel and copper. FTIR of the copper sulphate powder was used for comparison with composite spectrum.

Determining the Amount of Copper(II) Ions in a Solution Using a Smartphone

Science.gov (United States)

Montangero, Marc

2015-01-01

When dissolving copper in nitric acid, copper(II) ions produce a blue-colored solution. It is possible to determine the concentration of copper(II) ions, focusing on the hue of the color, using a smartphone camera. A free app can be used to measure the hue of the solution, and with the help of standard copper(II) solutions, one can graph a…

Growth of micro-crystals in solution by in-situ heating via continuous wave infrared laser light and an absorber

Science.gov (United States)

Pathak, Shashank; Dharmadhikari, Jayashree A.; Thamizhavel, A.; Mathur, Deepak; Dharmadhikari, Aditya K.

2016-01-01

We report on growth of micro-crystals such as sodium chloride (NaCl), copper sulphate (CuSO4), potassium di-hydrogen phosphate (KDP) and glycine (NH2CH2COOH) in solution by in-situ heating using continuous wave Nd:YVO4 laser light. Crystals are grown by adding single walled carbon nanotubes (SWNT). The SWNTs absorb 1064 nm light and act as an in-situ heat source that vaporizes the solvent producing microcrystals. The temporal dynamics of micro-crystal growth is investigated by varying experimental parameters such as SWNT bundle size and incident laser power. We also report crystal growth without SWNT in an absorbing medium: copper sulphate in water. Even though the growth dynamics with SWNT and copper sulphate are significantly different, our results indicate that bubble formation is necessary for nucleation. Our simple method may open up new vistas for rapid growth of seed crystals especially for examining the crystallizability of inorganic and organic materials.

Sulphate analysis in uranium leach iron(III) chloride solutions by inductively coupled argon plasma spectrometry

International Nuclear Information System (INIS)

Nirdosh, I.; Lakhani, S.; Yunus, M.Z.M.

1993-01-01

Inductively coupled Argon Plasma Spectrometry is used for the indirect determination of sulphate in iron(III) chloride leach solution of Elliot Lake uranium ores via addition of a known amount of barium ions and analyzing for excess of barium. The ore contains ∼ 7 wt% pyrite, FeS 2 , as the major mineral which oxidizes to generate sulphate during leaching with Fe(III). The effects of pH, the concentrations of Fe(III) and chloride ions and for presence of ethanol in the test samples on the accuracy of analysis are studied. It is found that unlike the Rhodizonate method, removal of iron(III) from or addition of ethanol to the test sample prior to analysis are not required. Linear calibration curves are obtained. (author)

In-situ x-ray absorption study of copper films in ground water solutions

International Nuclear Information System (INIS)

Kvashnina, K.O.; Butorin, S.M.; Modin, A.; Soroka, I.; Marcellini, M.; Nordgren, J.; Guo, J.-H.; Werme, L.

2007-01-01

This study illustrates how the damage from copper corrosion can be reduced by modifying the chemistry of the copper surface environment. The surface modification of oxidized copper films induced by chemical reaction with Cl - and HCO 3 - in aqueous solutions was monitored by in situ X-ray absorption spectroscopy. The results show that corrosion of copper can be significantly reduced by adding even a small amount of sodium bicarbonate. The studied copper films corroded quickly in chloride solutions, whereas the same solution containing 1.1 mM HCO 3 - prevented or slowed down the corrosion processes

Sulphate removal from sodium sulphate-rich brine and recovery of barium as a barium salt mixture.

Science.gov (United States)

Vadapalli, Viswanath R K; Zvimba, John N; Mulopo, Jean; Motaung, Solly

2013-01-01

Sulphate removal from sodium sulphate-rich brine using barium hydroxide and recovery of the barium salts has been investigated. The sodium sulphate-rich brine treated with different dosages of barium hydroxide to precipitate barium sulphate showed sulphate removal from 13.5 g/L to less than 400 mg/L over 60 min using a barium to sulphate molar ratio of 1.1. The thermal conversion of precipitated barium sulphate to barium sulphide achieved a conversion yield of 85% using coal as both a reducing agent and an energy source. The recovery of a pure mixture of barium salts from barium sulphide, which involved dissolution of barium sulphide and reaction with ammonium hydroxide resulted in recovery of a mixture of barium carbonate (62%) and barium hydroxide (38%), which is a critical input raw material for barium salts based acid mine drainage (AMD) desalination technologies. Under alkaline conditions of this barium salt mixture recovery process, ammonia gas is given off, while hydrogen sulfide is retained in solution as bisulfide species, and this provides basis for ammonium hydroxide separation and recovery for reuse, with hydrogen sulfide also recoverable for further industrial applications such as sulfur production by subsequent stripping.

Copper-Sulfate Pentahydrate as a Product of the Waste Sulfuric Acid Solution Treatment

OpenAIRE

Marković, Radmila; Stevanović, Jasmina; Avramović, Ljiljana; Nedeljković, Dragutin; Jugović, Branimir; Stajić Trošić, Jasna; Gvozdenović, Milica M.

2012-01-01

The aim of this study is synthesis of copper-sulfate pentahydrate from the waste sulfuric acid solution-mother liquor generated during the regeneration process of copper bleed solution. Copper is removed from the mother liquor solution in the process of the electrolytic treatment using the insoluble lead anodes alloyed with 6 mass pct of antimony on the industrial-scale equipment. As the result of the decopperization process, copper is removed in the form of the cathode sludge and is precipit...

Influence of solutes on heavy ion induced void-swelling in binary copper alloys

International Nuclear Information System (INIS)

Leister, K.H.

1983-05-01

As radiation induced swelling of metals depends on their constitution, swelling of copper and copper alloys with low solute concentration is studied. Diffusion coefficients and solubility of solute in copper were used as criteria of selection of the alloys. The samples were irradiated by 200keV copper ions. Swelling and void densities were measured by transmission electron microscopy. The measurements show low dependence of swelling upon the diffusibility of the solute in the solvent and a strong dependence on their concentration. Alloys of 0.1at% solute show more swelling than pure copper, and alloys of 1at% show less swelling under the irradiation conditions. The different swelling behavior in Cu-Ni alloys is due to the different void densities. (orig.) [de

Copper-Sulfate Pentahydrate as a Product of the Waste Sulfuric Acid Solution Treatment

Science.gov (United States)

Marković, Radmila; Stevanović, Jasmina; Avramović, Ljiljana; Nedeljković, Dragutin; Jugović, Branimir; Stajić-Trošić, Jasna; Gvozdenović, Milica

2012-12-01

The aim of this study is synthesis of copper-sulfate pentahydrate from the waste sulfuric acid solution-mother liquor generated during the regeneration process of copper bleed solution. Copper is removed from the mother liquor solution in the process of the electrolytic treatment using the insoluble lead anodes alloyed with 6 mass pct of antimony on the industrial-scale equipment. As the result of the decopperization process, copper is removed in the form of the cathode sludge and is precipitated at the bottom of the electrolytic cell. By this procedure, the content of copper could be reduced to the 20 mass pct of the initial value. Chemical characterization of the sludge has shown that it contains about 90 mass pct of copper. During the decopperization process, the very strong poison, arsine, can be formed, and the process is in that case terminated. The copper leaching degree of 82 mass pct is obtained using H2SO4 aqueous solution with the oxygen addition during the cathode sludge chemical treatment at 80 °C ± 5 °C. Obtained copper salt satisfies the requirements of the Serbian Standard for Pesticide, SRPS H.P1. 058. Therefore, the treatment of waste sulfuric acid solutions is of great economic and environmental interest.

A study of adsorption equilibrium on quaternary ammonium resin in uranyl sulphate solution

International Nuclear Information System (INIS)

Xu Genfu; Xu Jiazhong; Zhu Jinghua

1986-01-01

Adsorption equilibrium on quaternary ammonium resin in uranyl sulphate solution, which is similar to composition used in uranium hydrometallurgy, was studied by chemical equivalent method. In the given range, the ratio of HSO 4 - to SO 4 2- on the resin is dependent on concentration of H + and ionic strength (μ) of solution, but it is independent of other anions sorbed on the resin. When the solution has μ of 0.1 to 0.5, pH of 1.5 to 1.9 and 0.5 x 10 -3 to 2.0 x 10 -3 M of uranium, the value of n in complex UO 2 (SO 4 ) n 2-2n is 2.5 to 2.7. The uranium occupies about 30% to 50% of total resin capacity

Bronchography in dogs. Comparative study with two barium sulphate solutions

International Nuclear Information System (INIS)

Thibaut, J.; Gallardo, P.; Vargas, L.; Deppe, R.; Born, R.

1998-01-01

Two solutions of barium sulphate, 60 and 30% w/v, were compared with the ''overflow'' Bronchographic method. Two groups of eight healthy adult does of both sexes, weighing 7 to 18 kg were used for the study. The dogs were anaesthetised with thiopentone sodium 2% (20 mg/kg iv). After intubation, each dog received contrast medium by a catheter connected to a syringe, in a 9 mi dose. Two series of two x-rays plates were taken in left lateral recumbent, 3 and 6 min after administering the contrast medium and in ventrodorsal projection, 30 sec. later. The x-ray plates obtained were analysed and compared intra and inter group considering the advance speed of the contrast medium, the radiographic density and outlines. Adverse reactions were controlled

Interaction between copper and radiocesium in Indian mustard and sunflower grown in the hydroponic solution

International Nuclear Information System (INIS)

Shirong Tang; Xiaochang Wang

2002-01-01

Both Indian mustard and sunflower were grown in a hydroponic solution treated with different concentration activities of 134 Cs or with different amounts of copper or with both in order to investigate the interaction between copper and radiocesium. It was found that 134 Cs activity concentration applied in the nutrient solution exerted more influence on the uptake and translocation of copper by Indian mustard than by sunflower. Indian mustard grown in hydroponic solution containing certain levels of copper and being treated with higher 134 Cs activity concentration showed higher uptake of copper than sunflower. However, in the case of root copper concentrations, sunflower showed significantly higher copper immobilization by roots than Indian mustard. It was also found that the presence of copper the the hydroponic solution did modify radiocesium uptake by both species. The application of 1 mg/l in the growth medium could greatly increase the uptake of 134 Cs by both species. With 3 mg/l concentration of copper amended to the solution, the accumulation of 134 Cs by both species was decreased compared to the 1 mg/l copper treatment. These lines of evidence show that there is stronger interaction between copper and radiocesium in Indian mustard than in sunflower during the root uptake through nutrient solution. (author)

Sulphate content of the Muntimpa dam water and its impact on water quality

International Nuclear Information System (INIS)

Tembo, F; Shitumbanuma, V; Simukanga, S; Mudenda, G; Chileshe, P; Mulenga, S; Phiri, Y

2004-01-01

This article presents results of a study of the quality of water from Muntimpa Dam, a reservior of waste mine water released from the processing of copper and cobalt ores by Konkola Copper Mines(KCM) Plc in Chingola. The mine water is discharged into the local Muntimpa stream, a possible source of drinking and domestic water for the local population. The purpose of the study was to determine levels of sulphate in the dam and stream water and recommend possible methods of partial sulphate removal to levels below the recommended statutory limits and secondly, to assess the impact of high sulphate levels on water quality. Study methods included the sampling of water from the Muntimpa dam and catchment area. Stream water samples were collected about 5m from the stream banks while water samples from the dam were randomly collected from the near the centre of the dam at a depth of 50cm. Laboratory methods involved the determination of physical and chemical properties of the water using standard analytical techniques. Results of the study indicate that both total (2470mg/l) and available (1965mg/l) sulphate concentrations are higher than the recommended statutory limit for the discharge of sulphates into natural streams of 1500mg/l. From the study it is concluded that water in Muntimpa dam and stream is not suitable for drinking and other domestic use due to the high sulphate levels. From theorectical considerations, it was established that sulphate reduction could be achieved by addition of lime, which however had the consquence of increasing the pH of the water in excess of the recommended Zambian statutory value of nine, and would thus require an additional process to reduce the pH. (author)

Sulphate removal from uraniferous liquors

International Nuclear Information System (INIS)

Berger, B.

1983-01-01

A process for the recovery of uranium from liquor resulting from the attack of sulphur containing uraniferous ores by an alkaline solution of sodium carbonate and/or sodium bicarbonate is claimed. An ion exchange resin is used to separate the uranium from the solution of sodium carbonate and/or bicarbonate and sodium sulphate. The ion exchange resin is then eluted with a solution of ammonium carbonate and/or bicarbonate to provide an eluate containing ammonium uranyl tricarbonate, ammonium carbonate and/or bicarbonate and ammonium sulphate. The eluate is heated to boiling to convert the ammonium uranyl tricarbonate to ammonium uranate and/or diuranate. Ammonia, carbon dioxide and water vapor are released. The precipitated ammonium uranate and/or diuranate is separated from the remaining liquor and calcined to give uranium trioxide

Pourbaix Diagrams for Copper in 5 m Chloride Solution

International Nuclear Information System (INIS)

Beverskog, Bjoern; Pettersson, Sven-Olof

2002-12-01

Pourbaix diagrams for the copper in 5 molal chlorine at 5-100 deg C have been calculated. Predominance diagrams for dissolved copper containing species have also been calculated. Two different total concentrations of dissolved copper, 10 -4 and 10 -6 molal, have been used in the calculations. ChIoride is the predominating chlorine species in aqueous solutions. Therefore Pourbaix diagrams for chlorine can be used to discuss the effect of chloride solutions on the corrosion behavior of a metal. Presence of chloride increases the corrosion regions of copper at the expense of the immunity and passivity regions in the Pourbaix diagrams. Copper corrodes in 5 molal chloride by formation Of CuCl 3 2- in acid and alkaline solutions. At higher potentials in acid solutions CuCl 3 2- is oxidized to CuCl 2 (aq), which at increasing potentials can form CuCI + , Cu 2+ or CuClO 3 + . Copper passivates by formation of Cu 2 O(cr), CuO(cr), or CUO 2 3 Cu(OH) 2 (s). Cu 2 O(cr) does not form at [Cu(aq)] tot = 10 -6 molal in 5 m C1-, which results in a corrosion area between the immunity and passivity areas. Copper at the anticipated repository potentials and pH corrodes at 100 deg C at [Cu(aq)] tot = 10 -4 molal and at 80-100 deg C at [Cu(aq)] tot = 10 -6 molal. Copper at the anticipated repository potentials and pH can corrode at 80 deg C at [Cu(aq)] tot = 10 -4 molal and at 50 deg C at [Cu(aq)] tot = 10 -6 molal. The bentonite clay and copper canisters in the deep repository can be considered as a 'closed' system from macroscopic point of view. The clay barrier limits both inward diffusion of oxygen and aggressive anions as well as outward diffusion of corrosion products from the canisters. Both diffusion phenomena will drive the corrosion potential into the immunity area of the Pourbaix diagram for copper. The corrosion will thereby stop by an automatic mechanism. However, this is only valid if no macro cracks occur in the clay. The auto-stop is valid for the initial, main and

Incorporation of layered double nanomaterials in thin film nanocomposite nanofiltration membrane for magnesium sulphate removal

Science.gov (United States)

Hanis Tajuddin, Muhammad; Yusof, Norhaniza; Salleh, Wan Norharyati Wan; Fauzi Ismail, Ahmad; Hanis Hayati Hairom, Nur; Misdan, Nurasyikin

2018-03-01

Thin film nanocomposite (TFN) membrane with copper-aluminium layered double hydroxides (LDH) incorporated into polyamide (PA) selective layer has been prepared for magnesium sulphate salt removal. 0, 0.05, 0.1, 0.15, 0.2 wt% of LDH were dispersed in the trimesoyl chloride (TMC) in n-hexane as organic solution and embedded into PA layer during interfacial polymerization with piperazine. The fabricated membranes were further characterized to evaluate its morphological structure and membrane surface hydrophilicity. The TFN membranes performance were evaluated with divalent salt magnesium sulphate (MgSO4) removal and compared with thin film composite (TFC). The morphological structures of TFN membranes were altered and the surface hydrophilicity were enhanced with addition of LDH. Incorporation of LDH has improved the permeate water flux by 82.5% compared to that of TFC membrane with satisfactory rejection of MgSO4. This study has experimentally validated the potential of LDH to improve the divalent salt separation performance for TFN membranes.

Incorporation of layered double nanomaterials in thin film nanocomposite nanofiltration membrane for magnesium sulphate removal

Directory of Open Access Journals (Sweden)

Tajuddin Muhammad Hanis

2018-01-01

Full Text Available Thin film nanocomposite (TFN membrane with copper-aluminium layered double hydroxides (LDH incorporated into polyamide (PA selective layer has been prepared for magnesium sulphate salt removal. 0, 0.05, 0.1, 0.15, 0.2 wt% of LDH were dispersed in the trimesoyl chloride (TMC in n-hexane as organic solution and embedded into PA layer during interfacial polymerization with piperazine. The fabricated membranes were further characterized to evaluate its morphological structure and membrane surface hydrophilicity. The TFN membranes performance were evaluated with divalent salt magnesium sulphate (MgSO4 removal and compared with thin film composite (TFC. The morphological structures of TFN membranes were altered and the surface hydrophilicity were enhanced with addition of LDH. Incorporation of LDH has improved the permeate water flux by 82.5% compared to that of TFC membrane with satisfactory rejection of MgSO4. This study has experimentally validated the potential of LDH to improve the divalent salt separation performance for TFN membranes.

Extraction of indium from sulphate solutions with D2EHPA solutions using static mixers

International Nuclear Information System (INIS)

Nacevski, N.; Poposka, F.; Nikov, B.

1995-01-01

The possible use of static mixers as a reactor for the extraction of indium from sulphate solutions was investigated. The experimental work was focused on ''Kenics'' type static mixers, since these were found simplest and cheapest among a variety of models, and yet yielded acceptable preliminary results with low pressure drop along the reactor. A series of experiments was carried out in a stirred continuous flow reactor to compare the results. It was found that under certain (different) conditions both reactors perform satisfactorily. The energy consumption of a static mixer is of the same order of magnitude as that of a stirred vessel. The most significant achievement of the experimental work is establishing that the residence time in a static mixer is about two orders of magnitude less than that in a stirred reactor. (orig.)

Pourbaix Diagrams for Copper in 5 m Chloride Solution

Energy Technology Data Exchange (ETDEWEB)

Beverskog, Bjoern [OECD Halden Reactor Project (Norway); Pettersson, Sven-Olof [ChemIT, Nykoeping (Sweden)

2002-12-01

Pourbaix diagrams for the copper in 5 molal chlorine at 5-100 deg C have been calculated. Predominance diagrams for dissolved copper containing species have also been calculated. Two different total concentrations of dissolved copper, 10{sup -4} and 10{sup -6} molal, have been used in the calculations. ChIoride is the predominating chlorine species in aqueous solutions. Therefore Pourbaix diagrams for chlorine can be used to discuss the effect of chloride solutions on the corrosion behavior of a metal. Presence of chloride increases the corrosion regions of copper at the expense of the immunity and passivity regions in the Pourbaix diagrams. Copper corrodes in 5 molal chloride by formation Of CuCl{sub 3}{sup 2-} in acid and alkaline solutions. At higher potentials in acid solutions CuCl{sub 3}{sup 2-} is oxidized to CuCl{sub 2}(aq), which at increasing potentials can form CuCI{sup +}, Cu{sup 2+} or CuClO{sub 3}{sup +}. Copper passivates by formation of Cu{sub 2}O(cr), CuO(cr), or CUO{sub 2} 3 Cu(OH){sub 2}(s). Cu{sub 2}O(cr) does not form at [Cu(aq)]{sub tot} = 10{sup -6} molal in 5 m C1-, which results in a corrosion area between the immunity and passivity areas. Copper at the anticipated repository potentials and pH corrodes at 100 deg C at [Cu(aq)]{sub tot} = 10{sup -4} molal and at 80-100 deg C at [Cu(aq)]{sub tot} = 10{sup -6} molal. Copper at the anticipated repository potentials and pH can corrode at 80 deg C at [Cu(aq)]{sub tot} = 10{sup -4} molal and at 50 deg C at [Cu(aq)]{sub tot} = 10{sup -6} molal. The bentonite clay and copper canisters in the deep repository can be considered as a 'closed' system from macroscopic point of view. The clay barrier limits both inward diffusion of oxygen and aggressive anions as well as outward diffusion of corrosion products from the canisters. Both diffusion phenomena will drive the corrosion potential into the immunity area of the Pourbaix diagram for copper. The corrosion will thereby stop by an automatic

Electrochemical impedance study of copper in phosphate buffered solution

International Nuclear Information System (INIS)

Salimon, J.; Mohamad, M.; Yamin, B.M.; Kalaji, M.

2003-01-01

The processes occurring on the copper electrode surface in phosphate buffered solution were investigated using the Electrochemical Impedance Spectroscopy. The electrochemical behaviors of copper through their charge transfer resistance and double-layer capacitance at the onset of the hydrogen evolution region and the anodic passivation layer formation and diffusion of copper species at anodic potential regions are discussed. The specific adsorption of anions (hydroxide and/or H/sub 2/PO/sub 4/) occurred at potential less negative than -0.9V. Adsorbed hydrogen appeared at hydrogen evolution region at potential range of -1.5 to -1.0 V. The deposition of insoluble copper species occurred at anodic potential regions. (author)

Copper complexes as 'radiation recovery' agents

International Nuclear Information System (INIS)

Sorenson, J.R.J.

1989-01-01

Copper and its compounds have been used for their remedial effects since the beginning of recorded history. As early as 3000 BC the Egyptians used copper as an antiseptic for healing wounds and to sterilise drinking water; and later, ca 1550 BC, the Ebers Papyrus reports the use of copper acetate, copper sulphate and pulverised metallic copper for the treatment of eye infections. These historical uses of copper and its compounds are particularly interesting in the light of modern evidence concerning the use of certain copper complexes for the treatment of radiation sickness and more recently as an adjunct to radiotherapy for cancer patients. (author)

Kinetics and mechanism of protection of thymine from sulphate ...

Indian Academy of Sciences (India)

Unknown

The rate constant of sulphate radical anion with caffeic acid has been ... transfer of radical sites from base moiety to sugar moiety. Strand ... titrated with a standard ceric ammonium sulphate solution as reported by Kapoor et al.7. At room ...

Sulphate solubility and sulphate diffusion in oxide glasses: implications for the containment of sulphate-bearing nuclear wastes

International Nuclear Information System (INIS)

Lenoir, M.

2009-09-01

The thesis deals with sulphate solubility and sulphate diffusion in oxide glasses, in order to control sulphate incorporation and sulphate volatilization in nuclear waste glasses. It was conducted on simplified compositions, in the SiO 2 -B 2 O 3 -R 2 O (R = Li, Na, K, Cs), SiO 2 -B 2 O 3 -BaO and V 2 O 5 -B 2 O 3 -BaO systems. These compositions allowed us to study the influence of the nature of network-modifying ions (Li + , Na + , K + , Cs + or Ba 2+ ) and also of former elements (Si, B, V), on structure and properties of glasses. Sulphate volatility is studied in sodium borosilicate melts using an innovative technique of sulphate quantitation with Raman spectroscopy. This technique is useful to obtain kinetic curves of sulphate volatilization. The establishment of a model to fit these curves leads to the determination of diffusion coefficients of sulphate. These diffusion coefficients can thus be compared to diffusion coefficients of other species, determined by other techniques and presented in the literature. They are also linked to diffusion coefficients in relation with the viscosity of the melts. Concerning sulphate solubility in glasses, it depends on glass composition and on the nature of sulphate incorporated. Sulphate incorporation in alkali borosilicate glasses leads to the formation of a sulphate layer floating on top of the melt. Sulphate incorporation in barium borosilicate and boro-vanadate glasses leads to the crystallization of sulphate species inside the vitreous matrix. Moreover, sulphate solubility is higher in these glasses than in alkali borosilicates. Finally, exchanges between cations present in glasses and cations present in the sulphate phase are also studied. (author)

Thermometric titration of sulphate.

Science.gov (United States)

Williams, M B; Janata, J

1970-06-01

Direct thermometric titration of sulphate with a solution of barium perchlorate is proposed. The stoichiometry of the titration is shown to be critically dependent on the concentration of ethanol in the titration medium. The titration is rapid and suffers from only a few interferences.

Extraction of sulphates by long chain amines

International Nuclear Information System (INIS)

Boirie, Ch.

1959-05-01

The extraction of sulphuric acid by long chain amines in organic solution has been studied with a view to determining the value of the stability constants of the amine sulphates and bi-sulphates formed. We have concentrated chiefly on uranium sulphate and thorium sulphate. The formulae of the complexes extractable with amines have been established, as well as the corresponding dissociation constants. We have observed that for uranium sulphate the formula of the complex depends only on the nature of the amine, whereas for thorium this formula varies with the amine structure. From the formulae determined and the value of the constants calculated, we have been able to establish the best conditions for uranium and thorium extraction and also for a separation of these two elements. Finally we propose an application of this study to the determination of uranium in ores, where the separation of uranium by this method is particularly easy and complete. (author) [fr

Bacterial Reduction Of Barium Sulphate By Sulphate-Reducing Bacteria

Directory of Open Access Journals (Sweden)

Luptáková Alena

2015-12-01

Full Text Available Acid mine drainage (AMD is a worldwide problem leading to contamination of water sources. AMD are characterized by low pH and high content of heavy metals and sulphates. The barium salts application presents one of the methods for the sulphates removing from AMD. Barium chloride, barium hydroxide and barium sulphide are used for the sulphates precipitation in the form of barium sulphate. Because of high investment costs of barium salts, barium sulphide is recycled from barium sulphate precipitates. It can be recycled by thermic or bacterial reduction of barium sulphate. The aim of our study was to verify experimentally the possibility of the bacterial transformation of BaSO4 to BaS by sulphate-reducing bacteria. Applied BaSO4 came from experiments of sulphates removal from Smolnik AMD using BaCl2.

Removal of sulphates from waste waters by sulphate-reducing bacteria

Directory of Open Access Journals (Sweden)

Luptáková Alena

2002-03-01

Full Text Available are present in almost all types of water, usually as a simple anion SO42-. The sulphates together with hydrogencarbonates and chlorides are principal anions in natural waters. In typical underground and surface waters, the concentration of sulphates is in the range from ten to hundreds milligrams per litre.Nowadays, the importance of the control of sulphate concentration in waste waters increases. According to the Slovak legislation the limit concentration of sulphates in surface and drinking waters is 250 mg.l-1 . In rivers the contents of sulphates increases mainly by the discharge of waste waters, which are coming mainly from chemical, textile, metallurgical, pharmaceutical, paper and mining industry. The concentration of sulphates in these waters is in the order of grams per litre.Many technologies for the sulphates removal from waste waters exist, including biologico-chemical processes. The principle of one of these methods is the reduction of sulphates by sulphate-reducing bacteria to hydrogen-sulphide.The objective of this work was to study the effect of initial sulphates concentration on the activity of anaerobic sulphate reducers as well as the kinetics of the anaerobic sulphate reduction. The batch reactor was used at temperature of 30°C and pH 7,5. Lactate was used as the carbon source.

Antimicrobial activity of copper against organisms in aqueous solution: a case for copper-based water pipelines in hospitals?

Science.gov (United States)

Cervantes, Hilda I; Alvarez, Jose A; Muñoz, Juan M; Arreguín, Virginia; Mosqueda, Juan L; Macías, Alejandro E

2013-12-01

An association exists between water of poor quality and health care-associated infections. Copper shows microbiocidal action on dry surfaces; it is necessary to evaluate its antimicrobial effect against organisms in aqueous solution. The objective was to determine the in vitro antimicrobial activity of copper against common nosocomial pathogens in aqueous solution. Copper and polyvinyl chloride containers were used. Glass was used as control material. Fourteen organisms isolated from hospital-acquired infections, and 3 control strains were tested. Inocula were prepared by direct suspension of colonies in saline solution and water in each container tested. Bacterial counts in colony-forming units (CFU)/mL were determined at the beginning of the experiment; at 30 minutes; and at 1, 2, 24, and 48 hours. Organisms in glass and polyvinyl chloride remained viable until the end of the experiment. Organisms in copper showed a reduction from more than 100,000 CFU/mL to 0 CFU/mL within the first 2 hours of contact (F > 4.29, P water for human use, particularly in hospitals. Copyright © 2013 Association for Professionals in Infection Control and Epidemiology, Inc. Published by Mosby, Inc. All rights reserved.

Removal of copper ions from aqueous solutions by means of micellar-enhanced ultrafiltration

Directory of Open Access Journals (Sweden)

Kowalska Izabela

2017-01-01

Full Text Available The aim of the study was to assess the usefulness of micellar–enhanced ultrafiltration (MEUF for removal of copper ions from water solutions in comparison with classic ultrafiltration process. The tests were conducted in a semi–pilot membrane installation with the use of ultrafiltration module KOCH/ROMICON® at a transmembrane pressure of 0.05 MPa. The effect of concentration of copper ions on ultrafiltration process efficiency was investigated. The second part of the tests concerned the removal of copper ions by MEUF under wide range of anionic surfactant concentration (0.25, 1, and 5 CMC (critical micelle concentration. Concentration of copper ions in model solutions was equal to 5, 20, and 50 mg Cu/L. Furthermore, the effect of surfactant leakage to the permeate side during filtration was evaluated. Conducted experiments confirmed effectiveness of MEUF in copper ions removal. For the highest copper concentration in the feed (i.e. 50 mg/L, the average concentration of copper ions in the permeate ranged from 1.2–4.7 mg Cu/L depending on surfactant concentration. During filtration experiments, UF module exhibited stable transport properties for model solutions containing copper. For the highest concentration of metal, the decrease of permeate flux did not exceed 11% after 60 minutes of filtration. In the presence of the surfactant, a slight deterioration of transport properties was observed.

Studies on the sorption behaviours of Th(IV) and U(VI) from aqueous sulphate solutions using impregnated resin

International Nuclear Information System (INIS)

Khatab, A.F.; Sheta, M.E.; Mahfouz, M.G.; Tolba, A.A.

2007-01-01

The sorption behaviours of thorium (IV) and uranium (VI) from aqueous sulphate solutions have been studied using n-dodecylamine and tri-n-octylamine (TOA) dissolved in benzene and impregnated onto amberlite XAD-4 (styrene-divinyl benzene copolymer). The sorption behaviours were evaluated as a function of free acidity, salting out effect, ph value, equilibrium time, V/m ratio, initial metal ion concentration, loaded amine concentration and sorption temperature. The equilibrium time for Th(IV) and U(VI) sorption from aqueous sulphate solution was found to be 90 and 60 minutes, respectively. The sorption of Th(IV) was quantitatively at ph range 3.7-4.3 and at 4.3-5.2 for U(VI). The sorption capacity of the impregnated resin was determined by batch method and it was found to be 0.031 and 0.033 mmol/g for Th(IV) and U(VI), respectively. Elution of Th(IV) from thorium-loaded impregnated resin was quantitatively achieved by using 2 mol/l HNO 3 and by using 0.1 mol/l HCl for U(VI)

Substituted benzotriazoles as inhibitors of copper corrosion in borate buffer solutions

Science.gov (United States)

Agafonkina, M. O.; Andreeva, N. P.; Kuznetsov, Yu. I.; Timashev, S. F.

2017-08-01

The adsorption of substituted 1,2,3-benzotriazoles (R-BTAs) onto copper is measured via ellipsometry in a pure borate buffer (pH 7.4) and satisfactorily described by Temkin's isotherm. The adsorption free energy (-Δ G a 0 ) values of these azoles are determined. The (-Δ G a 0 ) values are found to rise as their hydrophobicity, characterized by the logarithm of the partition coefficient of a substituted BTA in a model octanol-water system (log P), grows. The minimum concentration sufficient for the spontaneous passivation of copper ( C min) and a shift in the potential of local copper depassivation with chlorides ( E pt) after an azole is added to the solution (i.e., Δ E = E pt in - E pt backgr characterizing the ability of its adsorption to stabilize passivation) are determined in the same solution containing a corrosion additive (0.01M NaCl) for each azole under study. Both criteria of the passivating properties of azoles (log C min and Δ E) are shown to correlate linearly with log P, testifying to the role played by surface activity of this family of organic inhibitors in protecting copper in an aqueous solution.

The effect of an induced copper deficiency on the total plasma ...

African Journals Online (AJOL)

The effect of a copper deficiency on certain aspects of reproduction in ewes was ... induced by using the copper antagonists cadmium, calcium and sulphate. .... sodium (Na), magnesium (MG), potassium (K), blood urea nitrogen (BUN) and ...

Copper recovery from slag by indirect bio leaching

International Nuclear Information System (INIS)

Mazuelos, A.; Iglesias, N.; Romero, R.; Forcat, O.; Carranza, F.

2009-01-01

The main source of copper loss from a smelter is copper in discard slag. Slag can contain Cu in concentrations very much higher than those of many ores. Cu is present in slag entrained in very small drops of matte, white metal and blister copper occluded in fayalitic phase. In this work, the technical viability of the BRISA process, that is based on the indirect bio leaching, for this residue has been proved. A sample of slag, containing 2 % of copper, has been chemical, granulometric and metallographic characterized and it has been leached with ferric sulphate solutions in agitated reactors. The influence of several variables have been investigated. Once the best operating conditions had been selecting and an economic estimation had been done (with very really attractive results), the leaching stage has been designed for a plant of 30 tonnes per hour capacity. Cu extractions higher than 70% can be achieved with a residence time of only five hours. Despite of Cu(II) concentration in fed is as high as 30 g/l, bio oxidation stage can supply Fe(III) demanded by ferric leaching stage. (Author) 17 refs

Reaction and nucleation mechanisms of copper electrodeposition on disposable pencil graphite electrode

Energy Technology Data Exchange (ETDEWEB)

Majidi, M.R. [Department of Analytical Chemistry, Faculty of Chemistry, University of Tabriz, 29th Bahman Bolvard, Tabriz 51664 (Iran, Islamic Republic of)], E-mail: sr.majidi@gmail.com; Asadpour-Zeynali, K.; Hafezi, B. [Department of Analytical Chemistry, Faculty of Chemistry, University of Tabriz, 29th Bahman Bolvard, Tabriz 51664 (Iran, Islamic Republic of)

2009-01-01

The reaction and nucleation mechanism of copper electrodeposition on disposable pencil graphite electrode (PGE) in acidic sulphate solution were investigated using cyclic voltammetry (CV) and chronoamperometry (CA) techniques, respectively. Electrochemical experiments were followed by morphological studies with scanning electron microscopy (SEM). The effect of some experimental parameters, namely copper concentration, pH, scan rate, background electrolyte, deposition potential, and conditioning surface of the electrode were described. At the surface of PGE, Cu{sup 2+} ions were reduced at -250 mV vs. SCE. It was found that electrodeposition of copper is affected by rough surface of PGE. The nucleation mechanisms were examined by fitting the experimental CA data into Scharifker-Hills nucleation models. The nuclei population densities were also determined by means of two common fitting models developed for three-dimensional nucleation and growth (Scharifker-Mostany and Mirkin-Nilov-Herrman-Tarallo). It was found that deposition potential and background electrolyte affect the distribution of the deposited copper. The morphology of the deposited copper is affected by background electrolyte.

Removal of copper and nickel contaminants from Si surface by use of cyanide solutions

International Nuclear Information System (INIS)

Fujiwara, N.; Liu, Y.-L.; Nakamura, T.; Maida, O.; Takahashi, M.; Kobayashi, H.

2004-01-01

The cleaning method using cyanide solutions has been developed to remove heavy metals such as copper (Cu) and nickel (Ni) from Si surfaces. Immersion of Si wafers with both Cu and Ni contaminants in potassium cyanide (KCN) solutions of methanol at room temperature decreases these surface concentrations below the detection limit of total reflection X-ray fluorescence spectroscopy of ∼3x10 9 atoms/cm 2 . UV spectra of the KCN solutions after cleaning of the Cu-contaminated Si surface show that stable copper-cyanide complexes are formed in the solution, leading to the prevention of the re-adsorption of copper in the solutions. From the complex stability constants, it is concluded that the Cu(CN) 4 3- is the most dominant species in the KCN solutions

Sulphate in Pregnancy

Directory of Open Access Journals (Sweden)

Paul A. Dawson

2015-03-01

Full Text Available Sulphate is an obligate nutrient for healthy growth and development. Sulphate conjugation (sulphonation of proteoglycans maintains the structure and function of tissues. Sulphonation also regulates the bioactivity of steroids, thyroid hormone, bile acids, catecholamines and cholecystokinin, and detoxifies certain xenobiotics and pharmacological drugs. In adults and children, sulphate is obtained from the diet and from the intracellular metabolism of sulphur-containing amino acids. Dietary sulphate intake can vary greatly and is dependent on the type of food consumed and source of drinking water. Once ingested, sulphate is absorbed into circulation where its level is maintained at approximately 300 μmol/L, making sulphate the fourth most abundant anion in plasma. In pregnant women, circulating sulphate concentrations increase by twofold with levels peaking in late gestation. This increased sulphataemia, which is mediated by up-regulation of sulphate reabsorption in the maternal kidneys, provides a reservoir of sulphate to meet the gestational needs of the developing foetus. The foetus has negligible capacity to generate sulphate and thereby, is completely reliant on sulphate supply from the maternal circulation. Maternal hyposulphataemia leads to foetal sulphate deficiency and late gestational foetal death in mice. In humans, reduced sulphonation capacity has been linked to skeletal dysplasias, ranging from the mildest form, multiple epiphyseal dysplasia, to achondrogenesis Type IB, which results in severe skeletal underdevelopment and death in utero or shortly after birth. Despite being essential for numerous cellular and metabolic functions, the nutrient sulphate is largely unappreciated in clinical settings. This article will review the physiological roles and regulation of sulphate during pregnancy, with a particular focus on animal models of disturbed sulphate homeostasis and links to human pathophysiology.

Isotopic methods of investigations of hydrodynamics in installations for hydrometallurgic processing of copper concentrates

International Nuclear Information System (INIS)

Stsheletski, M.; Urban'ski, T.S.

1979-01-01

Isotope methods have been presented of investigations of hydrodynamics of liquid and solid phases in pilot-scale installations for hydrometallurgic processing of copper concentrates: in the column installation for leaching; in the tubular reactor for copper reduction by hydrogen and in the installation for crystallization of magnesium sulphate under pressure conditions. The column leaching installation has been tested by pulse injection of two radioisotope indicators simultaneously. The copper concentrate was labelled by sorbed colloidal gold-198 and the liquid phase was labelled by solution of sodium chloride containing sodium-24. Measurements of the radiation intensities were registered by scintillation counters, working with a single-channel amplitude analyzer, integrators and counting rate monitors. According to the distribution of time of stay, by the moments method, number of powers of ideal intermixings in the cell model of flow of the both phases. In the tubular reactor process of copper reduction by hydrogen is going on in three phases: gas-liquid-solig phase. Hydrodynamic investigations in this instalation was done in the presence of air, water and copper powder. Water was labelled by sodium-24 and copper powder by copper-64. Changes of intensity of radiation were measured by scintillation counters, located along the installation and were registered by multichannel amplitude analyzer. Peckle number and longitudal dispersion factor were determined. In investigations of the solid phase hydrodynamics during crystallization of magnesium sulphate under elevated temperature and high pressure, as an indicator, isotope gold-198 has been used, by which crystalls of the solid phase were labelled, and isotope sodium-24 was added to a liquid. Simultaneousely were measured and registered by a single-channel analyzer intensity of radiation of both indicators. Mean time of stay and parameters of a mathematical model of the phases flow in this installation were

Anodic polarization behavior of pure copper in carbonate solutions

International Nuclear Information System (INIS)

Kawasaki, Manabu; Taniguchi, Naoki; Naitou, Morimasa

2008-03-01

Copper is one of the candidate materials for overpacks. The redox condition at the early stage of the post closure will be oxidizing. In order to understand the influence of environmental factors on the corrosion behavior of copper in such oxidizing environment, anodic polarization tests were performed in carbonate aqueous solution with varying the concentration of representative chemical species in groundwater. As the results of potentiodynamic and potentiostatic tests, anodic polarization behavior of pure copper was summarized as follows; Carbonate ion and bicarbonate ion promoted the passivation of pure copper, and suppressed the initiation of film breakdown. Chloride ion promoted both the active dissolution and initiation of film breakdown of pure copper. The influence of sulfate ion and pH was small, but the action of sulfate ion to the pure copper was similar to that of chloride ion, and the increase of pH was likely to promote the passivation and suppress the initiation of film breakdown. The film breakdown potential, Eb, was represented as a function of the ratio of aggressive ion and inhibiting ion such as [Cl - ]/[HCO 3 - ], [SO 4 2- ]/[HCO 3 - ]. When the ratio exceeds a certain value, the anodic polarization curve becomes active dissolution type so that no macroscopic film breakdown can not be occurred. The lower limit of Eb in passive type region was estimated to be about -200 mV vs. SCE. As the results of potentio static tests, the corrosion form near the Eb was uniform dissolution over the surface, but pitting corrosion and non-uniform corrosion occurred according to the condition of the test solution. Neither pitting corrosion nor non-uniform corrosion occurred at the potential below Eb in every test cases. (author)

Possible mechanisms for interaction of poly electrolytes with ions in aqueous solution

International Nuclear Information System (INIS)

Siyam, T.

1995-01-01

The interaction between the active groups of water soluble poly electrolytes such as polyacrylamide 'neutral polymers PAM', poly sodium acrylate 'anionic polymer PAANA', polyacrylamide-diallyamine-hydrochloride 'cationic polymer PAM-DAA-HCl and polyacrylamide-diallylethylamine-hydrochloride 'cationic polymer PAM-DAEA-HCl' with copper sulphate has been carried out under different experimental conditions. Spectroscopic studies show that the mechanism of the flock formation due to interaction between the polymer and copper sulphate is a bond formation between the active group of polymeric chains and copper sulphate. This bond formation depends on the nature of polymer chain. It was also found that the amide groups form complexes with hydrated cations, while both carboxylate-and ammonium groups interact by ion-exchange mechanism. The same studies were applied on polyacrylamideacrylic acid resin 'PAM-AA' resin and copper sulphate. The obtained results show that the resin interacts by the same mechanism, where the amide groups form a complex with hydrated cations, while the carboxylic group interacts by ion-exchange mechanism. 1 fig., 1 tab

2-Mercaptobenzothiazole doped chitosan/11-alkanethiolate acid composite coating: Dual function for copper protection

International Nuclear Information System (INIS)

Bao Qi; Zhang Dun; Wan Yi

2011-01-01

Chitosan (CS) hydrogel loaded with the well-known corrosion inhibitor 2-mercaptobenzothiazole (MBT) has been introduced into a composite coating to improve copper protection. This composite coating, which has both anticorrosion and antibacterial properties, was fabricated onto the surface of copper by combining a simple self-assembled monolayer technique with a sol-gel method. The anti-corrosion ability of the coating in 3.5 wt.% NaCl solution was investigated by electrochemical methods including potentiodynamic polarization and electrochemical impedance spectroscopy. The protection efficiency of the coating is 97.70%, calculated on the basis of the corrosion current density. The stability and integrity of the composite coating were evaluated by field emission scanning electron microscopy (FESEM) and energy dispersive spectrometry (EDS). The FESEM and EDS results suggest that the composite coating endows the copper substrate with antibacterial properties, as untreated bare copper underwent microbiologically influenced corrosion in the presence of sulphate reducing bacteria (SRB). This antibacterial feature was further confirmed by the SRB culture method. In a 3.5% NaCl solution and highly corrosive SRB culture media, the as-prepared CS based composite coating gave corrosion protection by exhibiting better barrier effects against the attack of aggressive environments.

Effect of Sulfide Concentration on Copper Corrosion in Anoxic Chloride-Containing Solutions

Science.gov (United States)

Kong, Decheng; Dong, Chaofang; Xu, Aoni; Man, Cheng; He, Chang; Li, Xiaogang

2017-04-01

The structure and property of passive film on copper are strongly dependent on the sulfide concentration; based on this, a series of electrochemical methods were applied to investigate the effect of sulfide concentration on copper corrosion in anaerobic chloride-containing solutions. The cyclic voltammetry and x-ray photoelectron spectroscopy analysis demonstrated that the corrosion products formed on copper in anaerobic sulfide solutions comprise Cu2S and CuS. And the corrosion resistance of copper decreased with increasing sulfide concentration and faster sulfide addition, owing to the various structures of the passive films observed by the atomic force microscope and scanning electron microscope. A p-type semiconductor character was obtained under all experimental conditions, and the defect concentration, which had a magnitude of 1022-1023 cm-3, increased with increasing sulfide concentration, resulting in a higher rate of both film growth and dissolution.

Coupled Transport/Reaction Modelling of Copper Canister Corrosion Aided by Microbial Processes

Energy Technology Data Exchange (ETDEWEB)

Liu, Jinsong [Royal Institute of Technology, Stockholm (Sweden). Dept. of Chemical Engineering and Technology

2006-04-15

Copper canister corrosion is an important issue in the concept of a nuclear fuel repository. Previous studies indicate that the oxygen-free copper canister could hold its integrity for more than 100,000 years in the repository environment. Microbial processes may reduce sulphate to sulphide and considerably increase the amount of sulphides available for corrosion. In this paper, a coupled transport/reaction model is developed to account for the transport of chemical species produced by microbial processes. The corroding agents like sulphide would come not only from the groundwater flowing in a fracture that intersects the canister, but also from the reduction of sulphate near the canister. The reaction of sulphate-reducing bacteria and the transport of sulphide in the bentonite buffer are included in the model. The depth of copper canister corrosion is calculated by the model. With representative 'central values' of the concentrations of sulphate and methane at repository depth at different sites in Fennoscandian Shield the corrosion depth predicted by the model is a few millimetres during 10{sup 5} years. As the concentrations of sulphate and methane are extremely site-specific and future climate changes may significantly influence the groundwater compositions at potential repository sites, sensitivity analyses have been conducted. With a broad perspective of the measured concentrations at different sites in Sweden and in Finland, and some possible mechanisms (like the glacial meltwater intrusion and interglacial seawater intrusion) that may introduce more sulphate into the groundwater at intermediate depths during future climate changes, higher concentrations of either/both sulphate and methane than what is used as the representative 'central' values would be possible. In worst cases. locally, half of the canister thickness could possibly be corroded within 10{sup 5} years.

Coupled Transport/Reaction Modelling of Copper Canister Corrosion Aided by Microbial Processes

International Nuclear Information System (INIS)

Jinsong Liu

2006-04-01

Copper canister corrosion is an important issue in the concept of a nuclear fuel repository. Previous studies indicate that the oxygen-free copper canister could hold its integrity for more than 100,000 years in the repository environment. Microbial processes may reduce sulphate to sulphide and considerably increase the amount of sulphides available for corrosion. In this paper, a coupled transport/reaction model is developed to account for the transport of chemical species produced by microbial processes. The corroding agents like sulphide would come not only from the groundwater flowing in a fracture that intersects the canister, but also from the reduction of sulphate near the canister. The reaction of sulphate-reducing bacteria and the transport of sulphide in the bentonite buffer are included in the model. The depth of copper canister corrosion is calculated by the model. With representative 'central values' of the concentrations of sulphate and methane at repository depth at different sites in Fennoscandian Shield the corrosion depth predicted by the model is a few millimetres during 10 5 years. As the concentrations of sulphate and methane are extremely site-specific and future climate changes may significantly influence the groundwater compositions at potential repository sites, sensitivity analyses have been conducted. With a broad perspective of the measured concentrations at different sites in Sweden and in Finland, and some possible mechanisms (like the glacial meltwater intrusion and interglacial seawater intrusion) that may introduce more sulphate into the groundwater at intermediate depths during future climate changes, higher concentrations of either/both sulphate and methane than what is used as the representative 'central' values would be possible. In worst cases. locally, half of the canister thickness could possibly be corroded within 10 5 years

Coupled Transport/Reaction Modelling of Copper Canister Corrosion Aided by Microbial Processes

Energy Technology Data Exchange (ETDEWEB)

Jinsong Liu [Royal Institute of Technology, Stockholm (Sweden). Dept. of Chemical Engineering and Technology

2006-04-15

Copper canister corrosion is an important issue in the concept of a nuclear fuel repository. Previous studies indicate that the oxygen-free copper canister could hold its integrity for more than 100,000 years in the repository environment. Microbial processes may reduce sulphate to sulphide and considerably increase the amount of sulphides available for corrosion. In this paper, a coupled transport/reaction model is developed to account for the transport of chemical species produced by microbial processes. The corroding agents like sulphide would come not only from the groundwater flowing in a fracture that intersects the canister, but also from the reduction of sulphate near the canister. The reaction of sulphate-reducing bacteria and the transport of sulphide in the bentonite buffer are included in the model. The depth of copper canister corrosion is calculated by the model. With representative 'central values' of the concentrations of sulphate and methane at repository depth at different sites in Fennoscandian Shield the corrosion depth predicted by the model is a few millimetres during 10{sup 5} years. As the concentrations of sulphate and methane are extremely site-specific and future climate changes may significantly influence the groundwater compositions at potential repository sites, sensitivity analyses have been conducted. With a broad perspective of the measured concentrations at different sites in Sweden and in Finland, and some possible mechanisms (like the glacial meltwater intrusion and interglacial seawater intrusion) that may introduce more sulphate into the groundwater at intermediate depths during future climate changes, higher concentrations of either/both sulphate and methane than what is used as the representative 'central' values would be possible. In worst cases. locally, half of the canister thickness could possibly be corroded within 10{sup 5} years.

Effect of dietary organic and inorganic copper supplement on ...

African Journals Online (AJOL)

The effect of dietary copper source and dosage on growth, apparent nutrient digestibility, trace mineral retention, ileal morphology and blood parameters of cockerel chicks were investigated using two hundred and forty (240) day-old chicks arranged in a 2 × 3 factorial arrangements involving 2 Cu sources (copper sulphate ...

Study of micellar solutions of the 'sodium lauryl sulphate-heavy water' system by using pulsed NMR

International Nuclear Information System (INIS)

Fouchet, C.

1972-01-01

This research thesis reports the study of the nuclear magnetic resonance of protons contained by micellar solutions of sodium lauryl sulphate and heavy water. Relaxation times have been measured with respect to various parameters: concentration, temperature, frequency. The author presents the main properties of micellar solutions and indicate the various possible movements. Then, he addresses the implemented technique, and shows that NMR is sensitive to short range interactions, and allows micellar movements to be studied over an extended rate range. Experimental results are then presented and interpreted [fr

Behavior of copper in acidic sulfate solution: Comparison with acidic chloride

Energy Technology Data Exchange (ETDEWEB)

Tromans, D.; Silva, J.C. [Univ. of British Columbia, Vancouver, British Columbia (Canada). Dept. of Metals and Materials Engineering

1997-03-01

The anodic polarization behavior of copper in a 0.1 M sulfuric acid (H{sub 2}SO{sub 4}) + 1 M sodium sulfate (Na{sub 2}SO{sub 4}) solution (pH = 2.0) was studied at room temperature under quiescent and stirred conditions. The behavior was compared with aqueous equilibria via construction of a potential-vs-pH (E-pH) diagram for the copper-sulfate-water (Cu-SO{sub 4}{sup 2}-H{sub 2}O) system. Interpretation of the behavior was aided by comparison with aqueous equilibria and polarization studies of copper in a 0.2 M hydrochloric acid (HCl) + 1 M sodium chloride (NaCl) solution(pH = 0.8). The initial anodic dissolution region in the acidic sulfate solution exhibited Tafel behavior with a slope consistent with formation of cupric ions (Cu{sup 2+}) whose rate of formation was charge-transfer controlled. At higher potentials, limiting current density (i{sub L}) behavior was observed under E-pH conditions that were consistent with formation of a film of copper sulfate pentahydrate (CuSO{sub 4} {degree} 5H{sub 2}O). Comparison of experimental i{sub L} values with those predicted by mass transport-controlled processes, using estimates of the diffusion layer thickness obtained from the mass transfer-influenced region of apparent Tafel behavior in the acidic chloride solution, were in sufficient agreement to indicate i{sub L} was controlled by the rate of dissolution of the CuSO{sub 4} {degree} 5H{sub 2}O film via transport of Cu{sup 2+} from the film-electrolyte interface into the bulk solution.

High emittance black nickel coating on copper substrate for space applications

Energy Technology Data Exchange (ETDEWEB)

Somasundaram, Soniya, E-mail: jrf0013@isac.gov.in; Pillai, Anju M., E-mail: anjum@isac.gov.in; Rajendra, A., E-mail: rajendra@isac.gov.in; Sharma, A.K., E-mail: aks@isac.gov.in

2015-09-15

Highlights: • High emittance black nickel coating is obtained on copper substrate. • The effect of various process parameters on IR emittance is studied systematically. • Process parameters are optimized to develop a high emittance black nickel coating. • Coating obtained using the finalized parameters exhibited an emittance of 0.83. • SEM and EDAX are used for coating characterization. - Abstract: Black nickel, an alloy coating of zinc and nickel, is obtained on copper substrate by pulse electrodeposition from a modified Fishlock bath containing nickel sulphate, nickel ammonium sulphate, zinc sulphate and ammonium thiocyanate. A nickel undercoat of 4–5 μm thickness is obtained using Watts bath to increase the corrosion resistance and adhesion of the black nickel coating. The effect of bath composition, temperature, solution pH, current density and plating time on the coating appearance and corresponding infra-red emittance of the coating is investigated systematically. Process parameters are optimized to develop a high emittance space worthy black nickel coating to improve the heat radiation characteristics. The effect of the chemistry of the plating bath on the coating composition was studied using energy dispersive X-ray analysis (EDAX) of the coatings. The 5–6 μm thick uniform jet black zinc–nickel alloy coating obtained with optimized process exhibited an emittance of 0.83 and an absorbance of 0.92. The zinc to nickel ratio of black nickel coatings showing high emittance and appealing appearance was found to be in the range 2.3–2.4.

Effect of grain size on corrosion of nanocrystalline copper in NaOH solution

International Nuclear Information System (INIS)

Luo Wei; Xu Yimin; Wang Qiming; Shi Peizhen; Yan Mi

2010-01-01

Research highlights: → Coppers display an active-passive-transpassive behaviour with duplex passive film. → Grain size variation has little effect on the overall corrosion behaviour of Cu. → Little effect on corrosion may be due to duplex passivation in NaOH solution. → Bulk nanocrystalline Cu show bamboo-like flake corrosion structure. - Abstract: Effect of grain size on corrosion of bulk nanocrystalline copper was investigated using potentiodynamic polarization measurements in 0.1 M NaOH solution. Bulk nanocrystalline copper was prepared by inert gas condensation and in situ warm compress (IGCWC) method. The grain sizes of all bulk nanocrystalline samples were determined to be 48, 68 and 92 nm using X-ray diffraction (XRD). Results showed that bulk coppers displayed an active-passive-transpassive behaviour with duplex passive films. From polycrystalline to nanocrystalline, grain size variation showed little effect on the overall corrosion resistance of copper samples.

The vapour pressures over saturated aqueous solutions of cadmium chloride, cadmium bromide, cadmium iodide, cadmium nitrate, and cadmium sulphate

International Nuclear Information System (INIS)

Apelblat, Alexander; Korin, Eli

2007-01-01

Vapour pressures of water over saturated solutions of cadmium salts (chloride, bromide, iodide, nitrate, and sulphate) were determined over the temperature range 280 K to 322 K and compared with the literature data. The vapour pressures determined were used to obtain the water activities, osmotic coefficients and the molar enthalpies of vaporization in the (cadmium salt + water) systems

The vapour pressures over saturated aqueous solutions of cadmium chloride, cadmium bromide, cadmium iodide, cadmium nitrate, and cadmium sulphate

Energy Technology Data Exchange (ETDEWEB)

Apelblat, Alexander [Department of Chemical Engineering, Ben Gurion University of the Negev, P.O. Box 653, Beer Sheva 84105 (Israel)]. E-mail: apelblat@bgu.ac.il; Korin, Eli [Department of Chemical Engineering, Ben Gurion University of the Negev, P.O. Box 653, Beer Sheva 84105 (Israel)

2007-07-15

Vapour pressures of water over saturated solutions of cadmium salts (chloride, bromide, iodide, nitrate, and sulphate) were determined over the temperature range 280 K to 322 K and compared with the literature data. The vapour pressures determined were used to obtain the water activities, osmotic coefficients and the molar enthalpies of vaporization in the (cadmium salt + water) systems.

A contribution to the study of CuSO4.5H2O solubility in aqueous media

International Nuclear Information System (INIS)

Juan, D. de; Meseguer, V. F.; Lozano, L. J.

1999-01-01

Pentahydrate copper sulphate (Blue vitriol) is a copper salt used in mineralogy as activator reagent in concentration methods by flotation for sulphide ores: In this work, crystallization conditions of copper sulphate solutions have been determined as a function of both temperature and sulphuric acidity. The results obtained showed that Cu 2+ concentration in the solution is mainly a direct function of the logarithm of temperature and the sulfuric acid concentration. The influence of Zn 2+ presence in copper sulphate solubility has been also studied at ambient temperature. Results obtained led to a multiple linear regression between Cu 2+ concentration in the solution and sulphuric acid and Zn 2+ concentrations in the medium. Finally, a comparison between the results obtained and data available in the literature is made. (Author) 5 refs

Sodium Sulphate Effect on Cement Produced with Building Stone Waste

Directory of Open Access Journals (Sweden)

Emre Sancak

2015-01-01

Full Text Available In this study, the blended cements produced by using the building stone waste were exposed to sulphate solution and the cement properties were examined. Prepared mortar specimens were cured under water for 28 days and then they were exposed to three different proportions of sodium sulphate solution for 125 days. Performances of cements were determined by means of compressive strength and tensile strength tests. The broken parts of some mortar bars were examined with scanning electron microscope (SEM. Besides, they were left under moist atmosphere and their length change was measured and continuously monitored for period of 125 days. In blended cements, solely cements obtained by replacing 10–20% of diatomites gave similar strength values with ordinary Portland cement (CEM I 42.5R at the ages of 7, 28, and 56 days. In all mortar specimens that included either waste andesite (AP or marble powder (MP showed best performance against very severe effective sodium sulphate solutions (13500 mg/L.

Cephradine as corrosion inhibitor for copper in 0.9% NaCl solution

Science.gov (United States)

Tasić, Žaklina Z.; Petrović Mihajlović, Marija B.; Radovanović, Milan B.; Simonović, Ana T.; Antonijević, Milan M.

2018-05-01

The effect of (6R,7R)-7-[[(2R)-2-amino-2-cyclohexa-1,4-dien-1-ylacetyl]amino]-3-methyl-8-oxo-5-thia-1-azobicyclo[4.2.0]oct-2-ene-2-carboxylic acid (cephradine) on corrosion behavior of copper in 0.9% NaCl solution was investigated. The electrochemical methods including the open circuit potential measurements, potentiodynamic polarization and electrochemical impedance spectroscopy measurements, scanning electron microscopy with energy dispersive X-ray spectroscopy and quantum chemical calculations were used for this investigation. According to the results obtained by potentiodynamic polarization, cephradine acts as mixed type inhibitor. Also, the results obtained by electrochemical impedance spectroscopy indicate that cephradine provides good copper protection in 0.9% NaCl solution. The inhibition efficiency of cephradine increases with increasing its concentration. The scanning electron microscopy with energy dispersive X-ray spectroscopy confirms that a protective layer is formed on the copper surface due to the adsorption of cephradine on the active sites on the copper surface. Adsorption of cephradine in 0.9% NaCl solution follows the Langmuir adsorption isotherm. Quantum chemical calculations are in agreement with results obtained by electrochemical measurements.

Yield of castor bean fertilized with sewage sludge and potassium and magnesium sulphate

Directory of Open Access Journals (Sweden)

Thâmara F. M. Cavalcanti

2015-08-01

Full Text Available ABSTRACTThe aim of this study was to evaluate the yield and nutrition of castor bean in response to fertilization with sewage sludge and potassium (K and magnesium (Mg sulphate. The experiment was carried out from January to July 2011. The treatments, in a randomized block design with three replicates, in a Nitosol, corresponded to a factorial scheme (2 x 4 +1: two doses of K and Mg sulphate combined with four doses of sewage sludge (0, 2.60, 5.20 and 10.40 t ha-1, dry basis, applied based on its nitrogen (N content and the N requirement for the crop and an additional treatment with NPK. The castor bean grain yield fertilized with sewage sludge did not differ from conventional fertilization, with the maximum value achieved at a dose of 7.5 t ha-1 of sewage sludge. The fertilization with sewage sludge increased zinc and copper levels in the soil to values close to or higher than those in conventional fertilization, without any influence on the concentrations in the leaf. Fertilization with K and Mg sulphate increased the levels of these cations in the soil without affecting the concentrations in the leaves. The fertilization with sewage sludge increased the contents of organic matter, sulfur, zinc, iron, copper and boron in the soil, and manganese and boron in castor bean leaves.

Selective Recovery Of Copper From Solutions After Bioleaching Electronic Waste

Directory of Open Access Journals (Sweden)

Willner Joanna

2015-06-01

Full Text Available Research on selective extraction of copper from solution after bioleaching grounded printed circuit boards (PCBs using LIX 860N-IC were conducted. The effect of LIX 860N-IC concentration, phase ratio and influence of initial pH value of aqueous phase on the extraction of copper and iron was examined. It was found that the extraction rate of copper increases with the LIX 860N-IC concentration. Best results of Cu extraction (98 % were achieved with extractant concentration of 5 % and pH 1.9. Higher pH value of aqueous phase (pH=2.4 is conducive to the simultaneous effect of Fe co-extraction.

Electrochemical study in the molten sodium acid sulphate - potassium acid sulphate eutectic

International Nuclear Information System (INIS)

Le Ber, F.

1964-01-01

The general properties of the NaHSO 4 - KHSO 4 molten eutectic resemble those of neutral sulphates and those of concentrated H 2 SO 4 . We have been able to show the existence in solution of the ions HSO - 4 SO 2- 4 , and H 3 O + , these last being formed by the action of the HSO - 4 ions on dissolved H 2 O. The electro-active zone with a polished platinum electrode is limited in oxidation by the ions H 3 O + and SO 2- 4 , and in reduction by the protons of HSO - 4 . We have compared the electro-active zones obtained with different electrodes (Ag-Au-graphite-mercury). We have considered the dissolution of a few metallic oxides and halides. This work shows the role as O 2- ion acceptors of HSO - 4 ions. We have undertaken an electro-chemical study of a few oxido-reduction Systems: H + / H 2 , Ag↓ / Ag (1), the vanadium and uranium Systems, those of mercury Hg↓ / Hg 2- 2 and of gold Au/Au 3+ , then of the attack by the solvent of a few common metals such as aluminium, iron, copper and nickel. The study of silver Systems has made it possible to obtain the solubility products of AgCl and AgBr and to consider the possibility of coulometric titration Cl - ions with Ag + ions. We have shown the existence of various chemical species of vanadium which may exist in the molten eutectic. (author) [fr

Ontario Hydro studies on copper corrosion under waste disposal conditions

International Nuclear Information System (INIS)

Lam, K.W.

1990-01-01

The corrosion rate of copper is generally greater in aerated solutions containing sulphide; also, in the presence of sulphide there is the fear that pitting may occur. Experiments have been carried out to study the corrosion of copper in deaerated groundwater/bentonite slurries with and without added sulphide for exposure periods from two months to one year. The groundwater contains 6500 ppm of chloride and 1000 ppm of sulphate. Tests were also performed in the presence of a 150 rad/h radiation field. In deaerated slurries at 75C the corrosion rate is less than 2 μm/a. With one addition of 10 mg/l sulphide, the rate increases by a factor of ten. With daily sulphide additions to deaerated solutions the corrosion rate initially falls but then rises and stabilizes after 15 days. In aerated solutions the corrosion increases over the first 25 days and then stabilizes. The corrosion rate of copper reached a steady value in 15 to 30 days. Rates are higher in aerated solutions, but the effect of adding sulphide is not so marked in aerated solutions as in unaerated solutions. The highest corrosion rate, less than 150 μm/a, was observed in aerated slurries saturated with sulphide. For deaerated solutions in the absence of sulphide the corrosion rate increases with temperature, but in aerated solutions the rate decreases. For solutions containing added sulphide the influence of temperature is negligible. The effect of a radiation field may be beneficial; in the presence of a radiation field the corrosion rate is less than 20 μm/a. After descaling the coupons showed a high density of irregularly shaped pits both in the presence and absence of sulphide, resulting from intergranular attack. The pitting factor for the highest corrosion rate is around 15

Recovery of copper and cyanide from waste cyanide solutions using emulsion liquid membrane with LIX 7950 as the carrier.

Science.gov (United States)

Xie, Feng; Wang, Wei

2017-08-01

The feasibility of using emulsion liquid membranes (ELMs) with the guanidine extractant LIX 7950 as the mobile carrier for detoxifying copper-containing waste cyanide solutions has been determined. Relatively stable ELMs can be maintained under suitable stirring speed during mixing ELMs and the external solution. Effective extraction of copper cyanides by ELMs only occurs at pH below 11. High copper concentration in the external phase and high volume ratio of the external phase to ELMs result in high transport rates of copper and cyanide. High molar ratio of cyanide to copper tends to suppress copper extraction. The presence of thiocyanate ion significantly depresses the transport of copper and cyanide through the membrane while the thiosulfate ion produces less impact on copper removal by ELMs. Zinc and nickel cyanides can also be effectively extracted by ELMs. More than 90% copper and cyanide can be effectively removed from alkaline cyanide solutions by ELMs under suitable experimental conditions, indicating the effectiveness of using the designed ELM for recovering copper and cyanide from waste cyanide solutions.

Effects of in vitro copper sulphate supplementation on the ejaculated sperm characteristics in water buff aloes ( Bubalus bubalis

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Mehdi Tabassomi

2013-03-01

Full Text Available This study was carried out to investigate effects of copper sulphate (CuSO4 additive tosemen extenders on sperm parameters:progressive motility, viability, membrane integrityand DNA damage, after semen dilution and cryopreservation. Semen samples of 5 buffalobulls of 3-5 years old were collected at 5 different occasions during the autumn 2011. A totalnumber of 25 samples were used in each examination. Sperm progressive motility andviability were measured at 0 (T0, 60 (T1 and 120 (T2 min after diluting semen in tris-citricacid extender containing 0 (control, 0.004, 0.008, 0.016, 0.032 and 0.064 mg L-1CuSO4. Later,semen was diluted in a tris-citric acid-egg yolk-glycerol extender containing the sameamounts ofCuSO4, cooled to 4̊C and kept refrigerated for 4 hr to equilibrate, spermprogressive motility, viability, membrane integrity and DNA damage were estimated. Then,semen was packed in 0.5 mL French straws and frozen in liquid nitrogen. Later, the frozensemen was thawed in 37 ̊C water bath for 30 sec, and the same parameters as well as totalantioxidant capacity (TAC of the frozen-thawed semen were estimated. The results showedthat copper additive at the rate of 0.032 mg L-1gives a better protection of sperms throughthe process of dilution, equilibration and freeze-thawing than that in control and other Cuconcentrations, while 0.064 mg L-1CuSO4had deleterious effect on the sperm.

Copper complexation by tannic acid in aqueous solution

NARCIS (Netherlands)

Kraal, P.; Jansen, B.; Nierop, K.G.J.; Verstraten, J.M.

2006-01-01

The speciation of titrated copper in a dissolved tannic acid (TA) solution with an initial concentration of 4 mmol organic carbon ((OC)/l was investigated in a nine-step titration experiment (Cu/oC molar ratio = 0.0030-0.0567). We differentiated between soluble and insoluble Cu species by 0.45 mu m

Isotopic evolution of aqueous sulphate in northern Chile water

International Nuclear Information System (INIS)

Aravena, R.; Suzuki, O.; Fritz, P.; Pena, H.; Rauert, W.

1987-01-01

deposits in the Salares provides strong indication that groundwater sulphate was their precursor. The enriched values of the springs' sulphate suggest that oxidation of sulphide minerals is not the main source of the sulphate in the recharge area. The isotope content of the aqueous sulphate in these water could be generated by an input of marine sulphate of Permian age. However, the rocks in this area are mainly igneous and volcanic. A more likely sulphur source are sulphate minerals associated with sulphide minerals in these terrains. For example the sulphate in porphyry copper deposits, which ate abundant in the Chilean Andes, shows an isotope content between +6.8 per mille and +8.5 per mille for 18 O and +8.6 per mille and + 15.5 per mille for 34 S. In conclusion, the sulphate in the Pampa and Llamara water is probably of hydrothermal-magmatic and/or volcanic origin. It has been proposed that the 18 O isotope exchange between water and sulphate could be used as an age indicator. However, comparison of radiocarbon data in groundwater with the parameter 18 O sulphate - 18 O water does not show any correlation and, therefore, no age information can be deducted based on the 18 O evolution of the sulphate. (author)

Assessment of strains of Pseudomonas syringae pv. tomato from Tanzania for resistance to copper and streptomycin

DEFF Research Database (Denmark)

Shenge, K.C.; Wydra, K.; Mabagala, M.B.

2008-01-01

Fifty-six strains of Pseudomonas syringae pv. tomato (P.s. pv. tomato) were collected from tomato-producing areas in Tanzania and assessed for resistance to copper and antibiotics. The collection was done from three tomato-producing regions (Morogoro, Arusha and Iringa), representing three...... different ecological conditions in the country. After isolation and identification, the P. s. pv. tomato strains were grown on King's medium B (KB) amended with 20% copper sulphate (w/v). The strains were also assessed for resistance to antibiotics. Results indicated that there was widespread resistance...... strains of the pathogen were moderately resistant to copper sulphate, such that 54.0% of them were able to grow on the KB medium amended with 20% (w/v) of the copper compound....

Adsorption of uranium(VI) from sulphate solutions using Amberlite IRA-402 resin: Equilibrium, kinetics and thermodynamics study

International Nuclear Information System (INIS)

Solgy, Mostafa; Taghizadeh, Majid; Ghoddocynejad, Davood

2015-01-01

Highlights: • Adsorption of uranium from sulphate solutions by an anion exchange resin. • The effects of pH, contact time and adsorbent dosage were investigated. • The adsorption equilibrium is well described by the Freundlich isotherm model. • The adsorption kinetics can be predicted by the pseudo second-order model. • The adsorption is a physical, spontaneous and endothermic process. - Abstract: In the present study, adsorption of uranium from sulphate solutions was evaluated using Amberlite IRA-402 resin. The variation of adsorption process was investigated in batch sorption mode. The parameters studied were pH, contact time and adsorbent dosage. Langmuir and Freundlich isotherm models were used in order to present a mathematical description of the equilibrium data at three different temperatures (25 °C, 35 °C and 45 °C). The final results confirmed that the equilibrium data tend to follow Freundlich isotherm model. The maximum adsorption capacity of Amberlite IRA-402 for uranium(VI) was evaluated to be 213 mg/g for the Langmuir model at 25 °C. The adsorption of uranium on the mentioned anion exchange resin was found to follow the pseudo-second order kinetic model, indicating that chemical adsorption was the rate limiting-step. The values of thermodynamic parameters proved that adsorption process of uranium onto Amberlite IRA-402 resin could be considered endothermic (ΔH > 0) and spontaneous (ΔG < 0)

The Effect of Copper

African Journals Online (AJOL)

environment, where fishes are found, stuns them ... of earthen ponds are springing up near cocoa ... farm, which posses toxicological risk to farmed ... Veg. oil. 1.0. 1.0. 1.0. 1.0. 1.0. Copper sulphate 0. 1.0. 2.5. 5.0. 7.5. Total ..... Cellulase Production by Wild Strains of Aspergillus Niger, ... Mangrove Area of Lagos, Nigeria.

Colloidal copper in aqueous solutions: radiation-chemical reduction, mechanism of formation and properties

International Nuclear Information System (INIS)

Ershov, B.G.

1994-01-01

Colloidal copper was obtained upon γ-irradiation of aqueous solutions of divalent copper perchlorate in the presence of alcohol and polyethyleneimine (PEI). The sols were in the form of spherical particles 4 nm in diameter, which were promptly oxidized by oxygen or other oxidants. The copper ions were reduced on the surface of silver sols. The optical parameters of the obtained bimetallic particles were studied. The copper ions led to the broadening and shift of the absorption bands of the silver sols to the UV region

Recovery of uranium from uranium mine waters and copper ore leaching solutions

Energy Technology Data Exchange (ETDEWEB)

George, D R; Ross, J R [Salt Lake City Metallurgy Research Center, Salt Lake City, UT (United States)

1967-06-15

Waters pumped from uranium mines in New Mexico are processed by ion exchange to recover uranium. Production is approximately 200 lb U{sub 3}O{sub 8}/d from waters containing 5 to 15 ppm U{sub 3}O{sub 8}. Recoveries range from 80 to 90%. Processing plants are described. Uranium has been found in the solutions resulting from the leaching of copper-bearing waste rock at most of the major copper mines in western United States. These solutions, which are processed on a very large scale for recovery of copper, contain 2 to 12 ppm U{sub 3}O{sub 8}. Currently, uranium is not being recovered, but a potential production of up to 6000 lb U{sub 3}O{sub 8}/d is indicated. Ion exchange and solvent extraction research studies are described. (author)

Electrochemical behaviour of copper in N,N-dimethylformamide + 0.5 M potassium perchlorate solution

Directory of Open Access Journals (Sweden)

S. MENTUS

2000-09-01

Full Text Available The electrochemical deposition and dissolution of copper in 0.0025 M CuSO4 + N,N-dimethylformamide + 0.5 M KClO4 solution was examined by the rotating disc and potentiodynamic methods. Both platinum and copper were used as working electrodes. A wide polarization range –1 to +2 V vs. SCE, and several temperatures between 25 and 55°C were encompased. The Cu/electrolyte interface was found to be permanently out of equilibrium, as a consequence of the development of a passivating layer. In accordance with the classic theory of a copper electrode in acidified aqueous solutions, the cathodic and anodic Tafel lines of metallic copper define a unique value of the exchange current density, however, their slopes do not correspond to the classic theory.

Hydrometallurgical treatment of copper smelter dusts. Desarsenification of leaching solutions

International Nuclear Information System (INIS)

Alguacil, F.J.; Magne, L.; Navarro, P.; Simpson, J.

1996-01-01

Copper smelter dusts contain along with this metal, which is amenable for its recovery, a number of other metals (especially arsenic) which are considered as toxic. Different alternatives have been proposed for the treatment of such metallurgical residues and among them Hydrometallurgy shows good perspectives for its application in this field. In the present work different hydrometallurgical processes proposed for the treatment of copper smelter dusts are described and evaluated together with different alternatives given for the Desarsenification of the leaching solutions. (Author) 36 refs

Lead and copper removal from aqueous solutions by porous glass derived calcium hydroxyapatite

International Nuclear Information System (INIS)

Liang Wen; Zhan Lei; Piao Longhua; Ruessel, Christian

2011-01-01

Graphical abstract: . Adsorption of Pb 2+ increases with the increase in NaCl volume percentage (1:0%, 2:30%, 3:40%, 4:40%) of the Glass Derived Hydroxyapatite and reaches equilibrium after 24 h. Highlights: → Novel porous glass derived hydroxyapatite matrix is prepared. → Glass derived hydroxyapatite matrix adsorbs lead and copper ions in solutions effectively. → Two adsorption mechanisms including ion exchange theory and the dissolution and precipitation theory are involved in removal of the heavy metal ions from the solutions. - Abstract: A porous glass was prepared by sintering Na 2 O-CaO-B 2 O 3 glass powder with powdered sodium chloride. Subsequently, the sodium chloride was dissolved in water resulting in a highly porous material. A sample was prepared consisting of 60 vol% glass and 40 vol% salt which both had particle sizes 2 HPO 4 solutions at room temperature for 1 day. The porous glass derived hydroxyapatite matrix was then processed for removing lead and copper ions from aqueous solutions. The results showed that the glass derived calcium hydroxyapatite matrix effectively immobilizes lead and copper ions in solution. The adsorption mechanism was investigated by the X-ray Diffraction (XRD) and Scanning Electron Microscopy including Energy Dispersive X-Ray Spectrometry (SEM-EDX).

Effect of acetic acid on wet patterning of copper/molybdenum thin films in phosphoric acid solution

International Nuclear Information System (INIS)

Seo, Bo.-Hyun; Lee, Sang-Hyuk; Park, In-Sun; Seo, Jong Hyun; Choe, HeeHwan; Jeon, Jae-Hong; Hong, Munpyo; Lee, Yong Uk; Winkler, Joerg

2011-01-01

Copper metallization is a key issue for high performance thin film transistor (TFT) technology. A phosphoric acid based copper etchant is a potentially attractive alternative to the conventional hydrogen peroxide based etchant due to its longer-life expectancy time and higher stability in use. In this paper, it is shown that amount of the acetic acid in the phosphoric based copper etchant plays an important role in controlling the galvanic reaction between the copper and the molybdenum. As the concentration of acetic acid in the phosphoric mixture solution increased from 0 M to 0.4 M, the measured galvanic current density dropped from 32 mA/cm 2 to 26 mA/cm 2 , indicating that the acetic acid induces the lower galvanic reaction between the copper and the molybdenum in the solution. From the XPS analysis, with the addition of the acetic acid, the thickness of the protective MoO 2 passive film covering the molybdenum surface grew and the dissolution rate of the molybdenum thin film decreased. However, the dissolution rate of the copper thin film increased as the concentration of acetic acid in the mixture solution increased.

Effect of acetic acid on wet patterning of copper/molybdenum thin films in phosphoric acid solution

Energy Technology Data Exchange (ETDEWEB)

Seo, Bo.-Hyun; Lee, Sang-Hyuk; Park, In-Sun [Department of Materials Engineering, Korea Aerospace University, Hwajeon, Goyang, Gyonggi-do 412-791 (Korea, Republic of); Seo, Jong Hyun, E-mail: jhseo@kau.ac.kr [Department of Materials Engineering, Korea Aerospace University, Hwajeon, Goyang, Gyonggi-do 412-791 (Korea, Republic of); Choe, HeeHwan; Jeon, Jae-Hong [School of Electronics, Telecommunications and Computer Engineering, Korea Aerospace University, Hwajeon, Goyang, Gyonggi-do 412-791 (Korea, Republic of); Hong, Munpyo [Display and Semiconductor Physics, Korea University (Korea, Republic of); Lee, Yong Uk [PETEC (The Printable Electronics Technology Centre) (United Kingdom); Winkler, Joerg [PLANSEE Metal GmbH, Metallwerk-Plansee-Str. 71A-6600, Reutte (Austria)

2011-08-01

Copper metallization is a key issue for high performance thin film transistor (TFT) technology. A phosphoric acid based copper etchant is a potentially attractive alternative to the conventional hydrogen peroxide based etchant due to its longer-life expectancy time and higher stability in use. In this paper, it is shown that amount of the acetic acid in the phosphoric based copper etchant plays an important role in controlling the galvanic reaction between the copper and the molybdenum. As the concentration of acetic acid in the phosphoric mixture solution increased from 0 M to 0.4 M, the measured galvanic current density dropped from 32 mA/cm{sup 2} to 26 mA/cm{sup 2}, indicating that the acetic acid induces the lower galvanic reaction between the copper and the molybdenum in the solution. From the XPS analysis, with the addition of the acetic acid, the thickness of the protective MoO{sub 2} passive film covering the molybdenum surface grew and the dissolution rate of the molybdenum thin film decreased. However, the dissolution rate of the copper thin film increased as the concentration of acetic acid in the mixture solution increased.

Inhibition of copper corrosion in sodium chloride solution by the self-assembled monolayer of sodium diethyldithiocarbamate

Energy Technology Data Exchange (ETDEWEB)

Liao, Q.Q., E-mail: liaoqq1971@yahoo.com.c [Key Lab of Shanghai Colleges and Universities for Electric Power Corrosion Control and Applied Electrochemistry, Shanghai Engineering Research Center of Energy - Saving in Heat Exchange Systems, Shanghai University of Electric Power, Shanghai 200090 (China); Yue, Z.W.; Yang, D. [Key Lab of Shanghai Colleges and Universities for Electric Power Corrosion Control and Applied Electrochemistry, Shanghai Engineering Research Center of Energy - Saving in Heat Exchange Systems, Shanghai University of Electric Power, Shanghai 200090 (China); Wang, Z.H. [Department of Chemistry, Tongji University, Shanghai 200092 (China); Li, Z.H. [Department of Chemistry, Fudan University, Shanghai 200433 (China); Ge, H.H. [Key Lab of Shanghai Colleges and Universities for Electric Power Corrosion Control and Applied Electrochemistry, Shanghai Engineering Research Center of Energy - Saving in Heat Exchange Systems, Shanghai University of Electric Power, Shanghai 200090 (China); Li, Y.J. [Department of Chemistry, Tongji University, Shanghai 200092 (China)

2011-05-15

Research highlights: DDTC is of low toxicity. DDTC SAM had good corrosion inhibition effects on copper in 3% NaCl solution. DDTC SAM was chemisorbed on copper surface by its S atoms. - Abstract: Sodium diethyldithiocarbamate (DDTC) self-assembled monolayer (SAM) on copper surface has been investigated by SERS and EDS and the results show that DDTC SAM is chemisorbed on copper surface by its S atoms with tilted orientation. Corrosion inhibition ability of DDTC SAM was measured in 3% NaCl solution using electrochemical methods. The impedance results indicate that the maximum inhibition efficiency of DDTC SAM can reach 99%. Quantum chemical calculations show that DDTC has relatively small {Delta}E between HOMO and LUMO and large negative charge in its two sulfur atoms, which facilitates the formation of a DDTC SAM on copper surface.

Investigation of copper(I sulphide leaching in oxidative hydrochloric acid solution

Directory of Open Access Journals (Sweden)

Branislav Marković

2015-12-01

Full Text Available Present work is focused on the copper (I sulphide leaching with sodium chloride in hydrochloric acid solution and with introduction of gaseous oxygen. Chemical reactions of leaching and their thermodynamic probabilities are predicted based on the literature data and products which were formed during the process and the overall leaching reaction was defined. The influence of temperature and time on the leaching degree of copper was experimentally determined. The quantity of dissolved copper increases with the increase of both investigated parameters. Elemental sulphur was formed as the main leaching product, precipitated at the particle surfaces and chloride ions have a role to disrupt the creation of this passive layer.

Removal of Copper(II) Ions in Aqueous Solutions Using Tannin-Rich Plants as Natural Bio-Adsorbents

Science.gov (United States)

Paksamut, J.; Boonsong, P.

2018-03-01

In this study, the purpose of our interest is to investigatethe adsorption behavior of copper (II) ions in aqueous solution using some tannin-rich plants as natural bio-adsorbents such as mangosteen peels (Garciniamangostana L.), cassava leaves (Manihotesculenta Crantz) and Thai copper pod leaves (Sennasiamea (Lam.)) as powder form in different dosage of adsorbent plant materials.The adsorption capacities at different pH of solution and contact time were performed.All the experiments in this studywere chosen at room temperature by batch technique. From the experimental results showed that cassava leaves gave better adsorbent properties than mangosteen peels and Thai copper pod leaves. The increasing dosage of all adsorbents and contact time have been found to increase adsorption capacities. In this respect, the adsorption capacities depend crucially on the adsorbents and contact time. The optimum pH of copper (II) ions adsorption was pH4. According to this work, it was observed that bioadsorbent materials from tannin-rich plants could be used to remove copper (II) ions from aqueous solutions.

Pitting corrosion of Al and Al-Cu alloys by ClO4- ions in neutral sulphate solutions

International Nuclear Information System (INIS)

Amin, Mohammed A.; Abd El Rehim, Sayed S.; Moussa, S.O.; Ellithy, Abdallah S.

2008-01-01

The influence of various concentrations of NaClO 4 , as a pitting corrosion agent, on the corrosion behaviour of pure Al, and two Al-Cu alloys, namely (Al + 2.5 wt% Cu) and (Al + 7 wt% Cu) alloys in 1.0 M Na 2 SO 4 solution was investigated by potentiodynamic polarization and potentiostatic techniques at 25 deg. C. Measurements were conducted under the influence of various experimental conditions, complemented by ex situ energy dispersive X-ray (EDX) and scanning electron microscopy (SEM) examinations of the electrode surface. In free perchlorate sulphate solutions, for the three Al samples, the anodic polarization exhibits an active/passive transition. The active dissolution region involves an anodic peak (peak A) which is assigned to the formation of Al 2 O 3 passive film on the electrode surface. The passive region extends up to 1500 mV with almost constant current density (j pass ) without exhibiting a critical breakdown potential or showing any evidence of pitting attack. For the three Al samples, addition of ClO 4 - ions to the sulphate solution stimulates their active anodic dissolution and tends to induce pitting corrosion within the oxide passive region. Pitting corrosion was confirmed by SEM examination of the electrode surface. The pitting potential decreases with increasing ClO 4 - ion concentration indicating a decrease in pitting corrosion resistance. The susceptibility of the three Al samples towards pitting corrosion decreases in the order: Al > (Al + 2.5 wt% Cu) alloy > (Al + 7 wt% Cu) alloy. Potentiostatic measurements showed that the rate of pitting initiation increases with increasing ClO 4 - ion concentration and applied step anodic potential, while it decreases with increasing %Cu in the Al samples. The inhibitive effect of SO 4 2- ions was also discussed

A novel polymeric leveller for the electrodeposition of copper from acidic sulphate bath: A spectroelectrochemical investigation

International Nuclear Information System (INIS)

Bozzini, Benedetto; D'Urzo, Lucia; Mele, Claudio

2007-01-01

The electrodeposition of copper has recently become a 'hot topic' due to its extensive application to the fabrication of interconnects in the integrated circuits (IC) manufacturing process. However, the proper composition of the electrochemical deposition (ECD) bath, and in particular the selection of the levelling agent, represents one of the crucial factors for an effective transition of Cu ECD towards the most advanced technology nodes. In this paper we report on the electrodeposition of Cu from acidic sulphate baths containing a potential innovative polymeric leveller: a benzyl-phenyl modified polyethyleneimine (BPPEI). This investigation was carried out by: (i) cyclic voltammetry (CV) at a rotating-disk electrode, (ii) in situ surface-enhanced Raman spectroscopy (SERS) during electrodeposition and (iii) scanning electron microscopy (SEM). CV results show that BPPEI acts as an inhibitor of the electrodeposition process, since it reduces the exchange current density and increases the cathodic Tafel slope. Mass transport limitations to the Cu(II) reduction process are essentially unaffected by the presence of BPPEI. SERS spectra show that BPPEI is adsorbed at the growing Cu cathode at all potentials of interest for electroplating. SEM micrographs prove that BPPEI acts as an efficient grain-refiner and suppressor of unstable 3D growth. Cathodic reactivity of BPPEI was proved by the analysis of CV features and potential-dependent SERS spectral changes

Flotation of copper-bearing shale in solutions of inorganic salts and organic reagents

Directory of Open Access Journals (Sweden)

Ratajczak Tomasz

2017-01-01

Full Text Available Flotation data on copper-bearing shale in aqueous solutions of inorganic electrolytes (NaCl, Na2SO4, KPF6, NH4Cl and organic reagents (ethylamine, propylamine as frothers were presented and discussed. The relationships between shale flotation, surface tension of aqueous solution and foam height during bubbling with air in the flotation system were presented. It has been found that flotation of shale in the presence of inorganic salts the yield was directly proportional to the surface tension of the aqueous solution of salt and inversely proportional to the height of the foam. On the other hand, for organic reagents solutions (short chain amines, a reverse effect has been observed in relation to the inorganic compounds studied, that is the yield of copper-bearing shale flotation and the foam height were inversely proportional to the surface tension of the amine solution.

Measurement and control in solution mining of copper and uranium

International Nuclear Information System (INIS)

Davidson, D.H.; Huff, R.V.; Sonstelie, W.E.

1978-01-01

The solution mining of deep-lying mineral deposits requires an integration of oilfield and extractive mineral technology. Although instrumentation is available to measure parameters relating to the oilfield components such as permeability, porosity and flow-logging, only limited services exist for monitoring leaching performance. This paper discusses the history of copper leaching, the need for solution mining development, and solution mining process descriptions. It discusses measurement requirements for deposit evaluation and the injection and production wellfields. It is concluded with a listing of desirable but unavailable instrumentation for further development of this technology

Electrical conductivity of solutions of copper(II) nitrate crystalohydrate in dimethyl sulfoxide

Science.gov (United States)

Mamyrbekova, Aigul K.; Mamitova, A. D.; Mamyrbekova, Aizhan K.

2016-06-01

Conductometry is used to investigate the electric conductivity of Cu(NO3)2 ṡ 3H2O solutions in dimethyl sulfoxide in the 0.01-2.82 M range of concentrations and at temperatures of 288-318 K. The limiting molar conductivity of the electrolyte and the mobility of Cu2+ and NO 3 - ions, the effective coefficients of diffusion of copper(II) ions and nitrate ions, and the degree and constant of electrolytic dissociation are calculated for different temperatures from the experimental results. It is established that solutions containing 0.1-0.6 M copper nitrate trihydrate in DMSO having low viscosity and high electrical conductivity can be used in electrochemical deposition.

Comparison of inorganic inhibitors of copper, nickel and copper-nickels in aqueous lithium bromide solution

International Nuclear Information System (INIS)

Munoz, A. Igual; Anton, J. Garcia; Guin-tilde on, J.L.; Herranz, V. Perez

2004-01-01

The electrochemical behavior of copper, nickel and two copper-nickel (Cu90/Ni10 and Cu70/Ni30) alloys in 850 g/L LiBr solution in the absence and presence of three different inorganic inhibitors (chromate CrO 4 2- , molybdate MoO 4 2- , and tetraborate B 4 O 7 2- ) has been studied. Differences in inhibition efficiency are discussed in terms of potentiodynamic and cyclic measurements. The best protection is obtained by adding chromate to the 850 g/L LiBr solution while the inhibition efficiencies of molybdate and tetraborate ions were not markedly high. Very aggressive anions, such as bromides, in the present experimental conditions, notably reduce the action of the less efficient molecules (molybdate and tetraborate), but not that of the most efficient ones (chromate). The results of the investigation show that the inhibiting properties depend on the nickel content in the alloy; this element improves the general corrosion resistance of the material in the sense that it shifts free corrosion potential towards more noble values and density corrosion currents towards lower levels. The nickel content in the alloy also enlarges the passivating region of the materials in chromate and molybdate-containing solution; furthermore it decreases the current passivating values to lower values. Nickel addition improves the localized corrosion resistance in the bromide media

X-ray diffraction phase analysis of crystalline copper corrosion products after treatment in different chloride solutions

International Nuclear Information System (INIS)

Chmielova, M.; Seidlerova, J.; Weiss, Z.

2003-01-01

The corrosion products Cu 2 (OH) 3 Cl, Cu 2 O, and CuCl 2 were identified on the surface of copper plates after their four days treating in three different sodium chloride, sodium/magnesium, and sodium/calcium chloride solutions using X-ray diffraction powder analysis. However, the quantitative proportions of individual corrosion products differ and depend on the type of chloride solution used. Treating of copper plates only in the sodium chloride solution produced the mixture of corrosion products where Cu 2 O is prevailing over the Cu 2 (OH) 3 Cl and CuCl 2 was not identified. The sample developed after treating of the cooper surface in the sodium/magnesium chloride solution contains Cu 2 (OH) 3 Cl and CuCl 2 prevailing over the Cu 2 O, while the sample developed after treatment of copper in sodium/calcium chloride solution contains Cu 2 (OH) 3 Cl prevailing over CuCl 2 and Cu 2 O was not identified

The Reclamation of Industrial Wastes Inclusive Sulphates by Sulphate-Reducing Bacteria

Directory of Open Access Journals (Sweden)

Mária Kušnierová

2004-12-01

Full Text Available The objective of our study was to verify experimentally the possibility of using coal mine drainage and gypsum from the „stabilizate“ (the final product from the combustion desulphurisation as the source of sulphate for the cultivation of SRB with the prospect of: purging of mine waste waters inclusive sulphates, recycling of desulphurisation agent (limestone and production of elemental sulphur from hydrogen sulphide. The results confirmed the theoretical assumptions on the use of gypsum, which forms the substantial component of „stabilizate“, as the source of sulphate for sulphate-reducing bacteria, which produce hydrogen sulphide in the process of bacterial reduction of sulphates. They also showed the possibility of recycling the desulphurisation agent – limestone, as well as the realistic alternative of using „stabilizate“ in the production of elemental sulphur which still represents an important raw material needed in chemical, paper or other industries.

Green chemical incorporation of sulphate into polyoxoanions of ...

Indian Academy of Sciences (India)

Green chemical incorporation of sulphate into polyoxoanions of molybdenum to nano level ... Keywords. Polyoxometalate; green synthesis; nanostructures; surfactant. ... The effects of reaction parameters such as concentration of surfactant, temperature and pH of solution on the synthesis of nanospheres were investigated.

Long-term corrosion of copper in a dilute anaerobic sulfide solution

Energy Technology Data Exchange (ETDEWEB)

Chen, J.; Qin, Z. [Department of Chemistry, University of Western Ontario, London, Ontario, N6A 5B7 (Canada); Shoesmith, D.W., E-mail: dwshoesm@uwo.ca [Department of Chemistry, University of Western Ontario, London, Ontario, N6A 5B7 (Canada)

2011-09-30

The mechanism of corrosion of oxygen-free copper has been studied in stagnant aqueous sulfide solutions using corrosion potential and electrochemical impedance spectroscopy (EIS) measurements. Film structure and composition were examined on surfaces and on cross-sections prepared by focused ion beam (FIB) milling using scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDS). Experiments were conducted in anaerobic 5 x 10{sup -5} mol dm{sup -3} Na{sub 2}S + 0.1 mol dm{sup -3} NaCl solutions for exposure periods up to 4000 h ({approx}167 days) to mimic (at least partially) the conditions that could develop on a copper nuclear fuel waste container in a deep geologic repository. The corrosion film formed was a single cellular Cu{sub 2}S layer with a non-uniform thickness. The film thickness increased approximately linearly with immersion time, which implied that the sulfide film formed on the Cu surface is non-protective under these conditions up to this exposure time. The film growth process was controlled by HS{sup -} diffusion partially in the aqueous solution in the pores in the cellular sulfide film and partially in the bulk of the aqueous solution.

Copper oxide thin films anchored on glass substrate by sol gel spin coating technique

Science.gov (United States)

Krishnaprabha, M.; Venu, M. Parvathy; Pattabi, Manjunatha

2018-05-01

Owing to the excellent optical, thermal, electrical and photocatalytic properties, copper oxide nanoparticles/films have found applications in optoelectronic devices like solar/photovoltaic cells, lithium ion batteries, gas sensors, catalysts, magnetic storage media etc. Copper oxide is a p-type semiconductor material having a band gap energy varying from 1.2 eV-2.1 eV. Syzygium Samarangense fruit extract was used as reducing agent to synthesize copper oxide nanostructures at room temperature from 10 mM copper sulphate pentahydrate solution. The synthesized nanostructures are deposited onto glass substrate by spin coating followed by annealing the film at 200 °C. Both the copper oxide colloid and films are characterized using UV-Vis spectroscopy, field emission scanning electron microscopy (FESEM) and energy dispersive spectroscopy (EDS) techniques. Presence of 2 peaks at 500 nm and a broad peak centered around 800 nm in the UV-Vis absorbance spectra of copper oxide colloid/films is indicative of the formation of anisotropic copper oxide nanostructures is confirmed by the FESEM images which showed the presence of triangular shaped and rod shaped particles. The rod shaped particles inside island like structures were found in unannealed films whereas the annealed films contained different shaped particles with reduced sizes. The elemental analysis using EDS spectra of copper oxide nanoparticles/films showed the presence of both copper and oxygen. Electrical properties of copper oxide nanoparticles are affected due to quantum size effect. The electrical studies carried out on both unannealed and annealed copper oxide films revealed an increase in resistivity with annealing of the films.

Patterned electrochemical deposition of copper using an electron beam

Directory of Open Access Journals (Sweden)

Mark den Heijer

2014-02-01

Full Text Available We describe a technique for patterning clusters of metal using electrochemical deposition. By operating an electrochemical cell in the transmission electron microscope, we deposit Cu on Au under potentiostatic conditions. For acidified copper sulphate electrolytes, nucleation occurs uniformly over the electrode. However, when chloride ions are added there is a range of applied potentials over which nucleation occurs only in areas irradiated by the electron beam. By scanning the beam we control nucleation to form patterns of deposited copper. We discuss the mechanism for this effect in terms of electron beam-induced reactions with copper chloride, and consider possible applications.

ADSORPTION OF COPPER FROM AQUEOUS SOLUTION BY ELAIS GUINEENSIS KERNEL ACTIVATED CARBON

Directory of Open Access Journals (Sweden)

NAJUA DELAILA TUMIN

2008-08-01

Full Text Available In this study, a series of batch laboratory experiments were conducted in order to investigate the feasibility of Elais Guineensis kernel or known as palm kernel shell (PKS-based activated carbon for the removal of copper from aqueous solution by the adsorption process. Investigation was carried out by studying the influence of initial solution pH, adsorbent dosage and initial concentration of copper. The particle size of PKS used was categorized as PKS–M. All batch experiments were carried out at a constant temperature of 30°C (±2°C using mechanical shaker that operated at 100 rpm. The single component equilibrium data was analyzed using Langmuir, Freundlich, Redlich-Peterson, Temkin and Toth adsorption isotherms.

Retenção de soluções de sulfatos por hidrogel de policrilamida = Retention of sulfhate solution by polierilamida hydrogel

Directory of Open Access Journals (Sweden)

Tedson Luis de Freitas Azevedo

2006-04-01

Full Text Available A utilização de hidrogel na agricultura brasileira, principalmente na silvicultura e fruticultura, está cada dia mais consolidado pela capacidade que ele possui de armazenar e disponibilizar água para as plantas. Este trabalho teve por objetivo estudar a capacidade deretenção de solução nutritiva pelo hidrogel quando submetido em diferentes soluções nutritivas de diferentes fertilizantes. Este estudo foi realizado no laboratório do Centro Técnico de Irrigação da Universidade Estadual de Maringá, Maringá, Estado do Paraná. Oexperimento constou de 26 tratamentos e 4 repetições, disposto em um esquema fatorial (5 x 5 mais um tratamento testemunha comum a todos os tratamentos, em um delineamento inteiramente casualizado. Os resultados mostraram que tanto as condutividades elétricas quanto as diferentes soluções de sulfatos interferiram na capacidade de retenção de solução nutritiva do hidrogel.The hydrogel use in the brazilian agriculture, mainly in the forestation, fruits field, and growth media, is being consolidated by its capacity of holding and release water (nutrient solution to plants. This work aimed to study the holding capacity of nutrient solutions by hydrogel when submitted into differents solutions from sulphates. This study was conducted out the Irrigation Technical Center of Universidade Estadual de Maringá, Maringá, Paraná State. Itwas conducted in a 5 x 5 factorial way (with 26 treatments and 04 replications and the randomized design. It was used as treatments 05 fertilizers sulphates base (ferrous sulphate, ammonium sulphate, zinc sulphate, copper sulphate, and magnesium sulphate and 05 doses (0.4; 0.8; 1.2; 1.6, and 2.0 g to each 500 g of distilled water. The distilled water treatment and hydrogel were used as control treatment. The hydrogel was hydrated for 24 hours for a later measure of holding capacity of nutrient solution. We noticed that besidesthe electric conductivity of nutrient solution the

Concentration of copper in muscles, liver, hair and feaces of growing rabbits fed diet supplemented with copper sulphate

Czech Academy of Sciences Publication Activity Database

Marounek, Milan; Skřivanová, V.; Volek, Z.; Březina, P.

2002-01-01

Roč. 10, č. 4 (2002), s. 167-170 ISSN 1257-5011 R&D Projects: GA AV ČR KSK5020115 Grant - others:GA NATO(XX) MO2-99-04 Keywords : copper retention * mineral metabolism * copper supplementation Subject RIV: FB - Endocrinology, Diabetology, Metabolism, Nutrition

Physicochemical analysis of cryocrystallization processes of aqueous solutions of yttrium, barium, copper nitrates and their mixtures

International Nuclear Information System (INIS)

Kulakov, A.B.; Mozhaev, A.P.; Tesker, A.M.; Churagulov, B.R.

1992-01-01

Products of fast hardening of aqueous solutions of different concentration of yttrium, barium copper nitrates and their mixtures including mixture of three nitrates with molar ratio equal to 1:2:3 used for synthesis of YBa 2 Cu 3 O 7-x HTSC by cryochemical technique, in liquid nitrogen, are studied using low-temperature, differential thermal and X-ray phase analyses. Aqueous solutions of barium, copper, yttrium nitrates are shown to belong to three different classes which differ in behaviour at fast cooling and subsequent slow heating. Cryogranulate at YBa 2 Cu 2 O 7-x synthesis using cryochemical technique represents mixture of X-ray amorphous Ba(NO 3 ) 2 , crystalline Cu(NO 3 ) 2 ·6H 2 O and ice, as well as, supercooled aqueous solution of yttrium and copper nitrates

Formation of salbutamol sulphate microparticles using solution enhanced dispersion by supercritical carbon dioxide

Directory of Open Access Journals (Sweden)

Abdolhossein Rouholamini Najafabadi

2005-01-01

Full Text Available Salbutamol sulphate (SS was precipitated by supercritical carbon dioxide (SC-CO2 using a homemade system at two different pressures. This process is characterized by spraying a methanolic solution of the drug into the supercritical fluid (SCF, extraction of the solvent by SC-CO2 and formation of drug particles. The morphology and size distribution of precipitated SS particles were characterized using scanning electron microscope and laser diffraction particle size analyzer respectively. FTIR spectra were used before and after processing to asses crystal modifications. Depending on the processing conditions, needle-like and flake-like particles with different size distributions were observed. The average size of the flake like particles was less than needle-like particles and the span parameter showed a narrower size distribution of the processed in comparison with the unprocessed materials. Analysis by FTIR showed that there was no significant effect on the structure of the drug under these processing conditions.

Electrochemical methods to study hydrogen production during interaction of copper with deoxygenated aqueous solution

International Nuclear Information System (INIS)

Lilja, Christina; Betova, Iva; Bojinov, Martin

2016-01-01

In some countries, spent nuclear fuel is planned to be encapsulated in canisters with a copper shell for corrosion protection, for further disposal in geologic repositories. The possibilities for corrosion after oxygen depletion must be evaluated, even if copper is considered to be immune in oxygen-free water. To follow the interaction of copper with deoxygenated aqueous solution, open-circuit potentiometric and electrochemical impedance measurements have been coupled to in-situ detection of cupric ion, dissolved molecular hydrogen and oxygen concentrations using electrochemical sensors. A kinetic model that considers the production of hydrogen as a catalytic process, the rate of which is proportional to the surface coverage of an intermediate species formed during interaction between copper and the solution is used to interpret the results. Kinetic parameters are estimated by a simultaneous fit of the experimental impedance spectra, the open circuit potential and cupric ion concentration as depending on temperature (22–70 °C) and exposure time (up to 720 h) to the model equations. Using the obtained values and a balance equation of hydrogen production on copper and its diffusion out of the cell through its walls, the kinetic parameters of this process are estimated by fitting dissolved molecular hydrogen concentration vs. time data at the three temperatures.

Synthesis of Copper Nanoparticles in Ethylene Glycol by Chemical Reduction with Vanadium (+2 Salts

Directory of Open Access Journals (Sweden)

Andrea Pietro Reverberi

2016-09-01

Full Text Available Copper nanoparticles have been synthesized in ethylene glycol (EG using copper sulphate as a precursor and vanadium sulfate as an atypical reductant being active at room temperature. We have described a technique for a relatively simple preparation of such a reagent, which has been electrolytically produced without using standard procedures requiring an inert atmosphere and a mercury cathode. Several stabilizing agents have been tested and cationic capping agents have been discarded owing to the formation of complex compounds with copper ions leading to insoluble phases contaminating the metallic nanoparticles. The elemental copper nanoparticles, stabilized with polyvinylpyrrolidone (PVP and sodium dodecyl sulphate (SDS, have been characterized for composition by energy dispersive X-ray spectroscopy (EDS, and for size by dynamic light scattering (DLS, and transmission electron microscopy (TEM, giving a size distribution in the range of 40–50 nm for both stabilizing agents. From a methodological point of view, the process described here may represent an alternative to other wet-chemical techniques for metal nanoparticle synthesis in non-aqueous media based on conventional organic or inorganic reductants.

Extraction of copper zinc and iron from hydrochloric acid solutions by means of different extractants

Energy Technology Data Exchange (ETDEWEB)

Zhivkova, Svetlana [Institute of Chemical Engineering - Bulgarian Academy of Sciences, Sofia (Bulgaria)

2011-07-01

The extraction of copper, zinc and iron from hydrochloric acid solutions has been studied. The experiments have been carried out using various solvents, involving different extraction mechanisms – solvating, anion-exchange, cation-exchange, bifunctional . Mixtures of these extractants have been also used. The extraction properties of these extractant mixtures toward copper, zinc and iron, the effect of used modifiers and diluents have been also investigated. Key words: Copper, Zinc, Iron, Extraction, Extractant, Modifier, Diluent.

Study of interaction of bismuth, strontium, calcium copper, lead nitrates solutions with sodium oxalate solution with the aim of HTSC synthesis

International Nuclear Information System (INIS)

Danilov, V.P.; Krasnobaeva, O.N.; Nosova, T.A.

1993-01-01

With the aim of developing a new technique for HTSC oxides synthesis on the base of combined sedimentation of hydroxy salts and their heat treatment is studied interaction of bismuth, strontium, calcium, copper and lead nitrates with alkali solution of sodium oxalate. Conditions for total sedimentation of all five metals from the solution are found. The phase composition of interaction products is determined. It is established that they are high-dispersed homogeneous mixture of three phases of variable composition: twin hydroxalate of copper-bismuth, lead hydroxalate and twin oxalate of strontium-calcium. After heat treatment of the phases are obtained the HTSC oxides

The impact of sulphate and magnesium on chloride binding in Portland cement paste

Energy Technology Data Exchange (ETDEWEB)

De Weerdt, K., E-mail: klaartje.d.weerdt@ntnu.no [Department of Structural Engineering, Norwegian University of science and Technology, Trondheim (Norway); SINTEF Building and Infrastructure, Trondheim (Norway); Orsáková, D. [Department of Civil Engineering, Technical University of Brno, Brno (Czech Republic); Geiker, M.R. [Department of Structural Engineering, Norwegian University of science and Technology, Trondheim (Norway)

2014-11-15

The effect of magnesium and sulphate present in sea water on chloride binding in Portland cement paste was investigated. Ground well hydrated cement paste was exposed to MgCl{sub 2}, NaCl, NaCl + MgCl{sub 2}, MgSO{sub 4} + MgCl{sub 2} and artificial sea water solutions with a range of concentrations at 20 °C. Chloride binding isotherms are determined and pH of the solutions were measured. A selection of samples was examined by SEM-EDS to identify phase changes upon exposure. The experimental data were compared with calculations of a thermodynamic model. Chloride binding from sea water was similar to chloride binding for NaCl solutions. The magnesium content in the sea water lead to a slight decrease in pH, but this did not result in a notable increase in chloride binding. The sulphate present in sea water reduces both chloride binding in C–S–H and AFm phases, as the C–S–H incorporates more sulphates instead of chlorides, and part of the AFm phases converts to ettringite.

Development and validation of a behavioural assay to measure the tolerance of Hediste diversicolor to copper

International Nuclear Information System (INIS)

Burlinson, Frazer C.; Lawrence, Andrew J.

2007-01-01

The behaviour of Hediste diversicolor from the Humber was investigated under different concentrations of copper sulphate. A range of behaviours were indicative of metal-stress. These included consistent attempts at burrowing, eversion of the proboscis and abnormal crawling. The bioassay itself consisted of exposing worms to increasing concentrations of copper sulphate and recording the concentration at which a stress response was elicited. The behavioural end-points were shown to be a good predictor of time of death of Fal estuary worms under acutely toxic conditions. The bioassay would therefore allow the separation of tolerance phenotypes without mortality to the worm. Worms were not affected by consecutive bioassays and it was proposed that tolerance to more than one metal could be determined for individual worms. - A non-destructive behavioural bioassay is developed to determine the copper tolerance of ragworms

Corrosion of copper alloys in sulphide containing district heting systems

DEFF Research Database (Denmark)

Thorarinsdottir, R.I.; Maahn, Ernst Emanuel

1999-01-01

Copper and some copper alloys are prone to corrosion in sulphide containing geothermal water analogous to corrosion observed in district heating systems containing sulphide due to sulphate reducing bacteria. In order to study the corrosion of copper alloys under practical conditions a test...... was carried out at four sites in the Reykjavik District Heating System. The geothermal water chemistry is different at each site. The corrosion rate and the amount and chemical composition of deposits on weight loss coupons of six different copper alloys are described after exposure of 12 and 18 months......, respectively. Some major differences in scaling composition and the degree of corrosion attack are observed between alloys and water types....

Sulphate partitioning into calcite: Experimental verification of pH control and application to seasonality in speleothems

Science.gov (United States)

Wynn, Peter M.; Fairchild, Ian J.; Borsato, Andrea; Spötl, Christoph; Hartland, Adam; Baker, Andy; Frisia, Silvia; Baldini, James U. L.

2018-04-01

Carbonate-associated sulphate (CAS) is a useful carrier of palaeoenvironmental information throughout the geologic record, particularly through its stable isotope composition. However, a paucity of experimental data restricts quantitative understanding of sulphate incorporation into carbonates, and consequently CAS concentrations and their diagenetic modifications are rarely interpreted. However, in the case of calcite speleothems, the remarkably high-resolution CAS records which are obtainable via modern microanalytical techniques represent a potentially invaluable source of palaeoenvironmental information. Here, we describe the results of controlled experiments of sulphate co-precipitation with calcite in freshwater solutions where pH, saturation state, and sulphate concentration were varied independently of each other. Solution pH is confirmed as the principal control on sulphate incorporation into calcite. The relative efficiency of incorporation was calculated as a partition coefficient DSO4 = (mSO4/mCO3)solid/(mSO4/mCO3)solution. High crystal growth rates (driven by either pH or saturation state) encouraged higher values of DSO4 because of an increasing concentration of defect sites on crystal surfaces. At low growth rates, DSO4 was reduced due to an inferred competition between sulphate and bicarbonate at the calcite surface. These experimental results are applied to understand the incorporation of sulphate into speleothem calcite. The experimentally determined pH-dependence suggests that strong seasonal variations in cave air PCO2 could account for annual cycles in sulphate concentration observed in stalagmites. Our new experimentally determined values of DSO4 were compared with DSO4 values calculated from speleothem-drip water monitoring from two caves within the Austrian and Italian Alps. At Obir cave, Austria, DSO4 (×105) varies between 11.1 (winter) and 9.0 (summer) and the corresponding figures for Ernesto cave, Italy, are 15.4 (winter) and 14

Leaching Characteristics of Uranium And Copper from Their Mineralization in the Carbonate Rich latosol of Abu-Thor Locality, South Western Sinai, Egypt

International Nuclear Information System (INIS)

El-Sheikh, E.M.; Ghazala, R.A.; Abdelwarith, A.; Salem, F.; Ali, S.

2015-01-01

The chemical processing of the poly-mineralized carbonate rich latosol ore occurring at Abu-Thor locality of south western Sinai area has been studied for the recovery of uranium and copper metal values. A technological sample assaying 700 ppm U and 9.7% Cu was collected. In the present study, two successive percolation leaching procedures were performed after determination of optimum leaching factors by agitation leaching process. The first was carried out for uranium recovery by using urea as organic leaching agent which was possible to achieve leaching efficiency exceeding 90.3%. This procedure was followed by a second one for copper recovery using ammonium hydroxide solution and ammonium carbonate. The obtained dissolution efficiency was about 93%. The leached metal values namely U and Cu from the studied ore were then extracted as marketable products in the form of ammonium diuranate and copper sulphate, respectively.

Selective and Efficient Solvent Extraction of Copper(II Ions from Chloride Solutions by Oxime Extractants

Directory of Open Access Journals (Sweden)

Zahra Kaboli Tanha

2016-06-01

Full Text Available Oxime extractants 3-tert-butyl-2-hydroxy-5-methyl benzaldehyde oxime (HL1 and 3-tert-butyl-2-hydroxy-5-methoxy benzaldehyde oxime (HL2 were synthesized and characterized by conventional spectroscopic methods. Suitable lipophilic nature of the prepared extractants allowed examining the ability of these molecules for extraction-separation of copper from its mixture with normally associated metal ions by performing competitive extraction experiments of Cu(II, Co(II, Ni(II, Zn(II, Cd(II and Pb(II ions from chloride solutions. Both ligands transfer selectively the copper ions into dichloromethane by a cation exchange mechanism. Conventional log-log analysis and isotherm curves showed that Cu(II ions are extracted as the complexes with 1:2 metal to ligand ratio by both extractants. Verification of the effect of the organic diluent used in the extraction of copper ions by HL1 and HL2 demonstrated that the extraction efficiency varies as: dichloromethane ~ dichloroethane > toluene > xylene > ethylacetate. Time dependency investigation of the extraction processes revealed that the kinetics of the extraction of copper by HL2 is more rapid than that of HL1. The application of the ligands for extraction-separation of copper ions from leach solutions of cobalt and nickel-cadmium filter-cakes of a zinc production plants was evaluated.

Effects of prior cold work on corrosion and corrosive wear of copper in HNO3 and NaCl solutions

International Nuclear Information System (INIS)

Yin Songbo; Li, D.Y.

2005-01-01

Effects of prior cold work on corrosion and corrosive wear behavior of copper in 0.1 M HNO 3 and 3.5% NaCl solutions, respectively, were investigated using electrochemical tests, electron work function measurements, and sliding corrosive wear tests with and without cathodic protection. Optical microscope and SEM were employed to examine the microstructure and worn surfaces. It was shown that, in general, the prior cold work raised the corrosion rate, but the effect differed in different corrosive media. In both the solutions, pure mechanical wear decreased with an increase in cold work. The prior cold work had a significant influence on the corrosive wear of copper, depending on the corrosive solution and the applied load. In the 0.1 M HNO 3 solution, the ratio of the wear loss caused by corrosion-wear synergism to the total wear loss increased with the cold work and became saturated when the cold work reached a certain level. In the 3.5% NaCl solution, however, this ratio decreased initially and then became relatively stable with respect to the cold work. It was observed that wear of copper in the 3.5% NaCl solution was larger than that in 0.1 M HNO 3 solution, although copper showed lower corrosion rate in the former solution. The experimental observations and the possible mechanisms involved are discussed

Evaluating portland cement concrete degradation by sulphate exposure through artificial neural networks modeling

International Nuclear Information System (INIS)

Oliveira, Douglas Nunes de; Bourguignon, Lucas Gabriel Garcia; Tolentino, Evandro; Costa, Rodrigo Moyses; Tello, Cledola Cassia Oliveira de

2015-01-01

A concrete is durable if it has accomplished the desired service life in the environment in which it is exposed. The durability of concrete materials can be limited as a result of adverse performance of its cement-paste matrix or aggregate constituents under either chemical or physical attack. Among other aggressive chemical exposures, the sulphate attack is an important concern. Water, soils and gases, which contain sulphate, represent a potential threat to the durability of concrete structures. Sulphate attack in concrete leads to the conversion of the hydration products of cement to ettringite, gypsum, and other phases, and also it leads to the destabilization of the primary strength generating calcium silicate hydrate (C-S-H) gel. The formation of ettringite and gypsum is common in cementitious systems exposed to most types of sulphate solutions. The present work presents the application of the neural networks for estimating deterioration of various concrete mixtures due to exposure to sulphate solutions. A neural networks model was constructed, trained and tested using the available database. In general, artificial neural networks could be successfully used in function approximation problems in order to approach the data generation function. Once data generation function is known, artificial neural network structure is tested using data not presented to the network during training. This paper is intent to provide the technical requirements related to the production of a durable concrete to be used in the structures of the Brazilian near-surface repository of radioactive wastes. (author)

Evaluating portland cement concrete degradation by sulphate exposure through artificial neural networks modeling

Energy Technology Data Exchange (ETDEWEB)

Oliveira, Douglas Nunes de; Bourguignon, Lucas Gabriel Garcia; Tolentino, Evandro, E-mail: tolentino@timoteo.cefetmg.br [Centro Federal de Educacao Tecnologica de Minas Gerais (CEFET-MG), Timoteo, MG (Brazil); Costa, Rodrigo Moyses, E-mail: rodrigo@moyses.com.br [Universidade de Itauna, Itauna, MG (Brazil); Tello, Cledola Cassia Oliveira de, E-mail: tellocc@cdtn.br [Centro de Desenvolvimento da Tecnologia Nucelar (CDTN/CNEN-MG), Belo Horizonte, MG (Brazil)

2015-07-01

A concrete is durable if it has accomplished the desired service life in the environment in which it is exposed. The durability of concrete materials can be limited as a result of adverse performance of its cement-paste matrix or aggregate constituents under either chemical or physical attack. Among other aggressive chemical exposures, the sulphate attack is an important concern. Water, soils and gases, which contain sulphate, represent a potential threat to the durability of concrete structures. Sulphate attack in concrete leads to the conversion of the hydration products of cement to ettringite, gypsum, and other phases, and also it leads to the destabilization of the primary strength generating calcium silicate hydrate (C-S-H) gel. The formation of ettringite and gypsum is common in cementitious systems exposed to most types of sulphate solutions. The present work presents the application of the neural networks for estimating deterioration of various concrete mixtures due to exposure to sulphate solutions. A neural networks model was constructed, trained and tested using the available database. In general, artificial neural networks could be successfully used in function approximation problems in order to approach the data generation function. Once data generation function is known, artificial neural network structure is tested using data not presented to the network during training. This paper is intent to provide the technical requirements related to the production of a durable concrete to be used in the structures of the Brazilian near-surface repository of radioactive wastes. (author)

Copper removal from aqueous solution using Aspergillus niger mycelia in free and polyurethane-bound form

Energy Technology Data Exchange (ETDEWEB)

Tsekova, K.; Ilieva, S. [Inst. of Microbiology, Bulgarian Academy of Sciences, Sofia (Bulgaria)

2001-07-01

This study assesses the ability of mycelia of Aspergillus niger B-77 (both free and immobilized on polyurethane foam) to remove copper from single-ion solution. All experiments were conducted using 0.5 mM solutions of CuSO{sub 4}.5H{sub 2} O. Mycelia immobilized on polyurethane foam cells showed a three-fold increase in uptake, compared with that of free cells. The efficiency of copper removal (mg Cu{sup 2+} removed/mg Cu{sup 2+} added) in a column system reached more than 99% before the break-through point was attained. (orig.)

Synthesis and thermal behavior of double copper and potassium pyrophosphate

International Nuclear Information System (INIS)

Ciopec, Mihaela; Muntean, Cornelia; Negrea, Adina; Lupa, Lavinia; Negrea, Petru; Barvinschi, Paul

2009-01-01

This paper presents the synthesis and thermal behavior of double copper and potassium pyrophosphate, which can be used as a PK fertilizer containing copper as micronutrient. In order to find the conditions for the synthesis of this compound from copper sulphate and potassium pyrophosphate, various Cu 2+ :P 2 O 7 4- molar ratios (0:1-2:1), various molar concentrations of the solutions (0.075; 0.1; 0.15 and 0.2 mol L -1 ) and various temperatures (25, 50, 75 and 100 o C) have been used. The solid product synthesized in optimum conditions for the separation of micronutrient copper from the reaction mass (Cu 2+ :P 2 O 7 4- molar ratio 1:1, concentration 0.1 mol L -1 ) was subjected to a complex study: chemical analysis, thermal analysis, energy dispersive X-ray spectroscopy, scanning electron microscopy and X-ray diffractometry. During heating up to 1000 o C, K 2 Cu 3 (P 2 O 7 ) 2 .3H 2 O loses the crystallization water; several transformations of the phosphates also take place: the decomposition of pyrophosphates to ortho-phosphates; the transformation of ortho-phosphates; the polymerization of a fraction of ortho-phosphates to amorphous phosphates with longer chains; the reorganization of ortho-phosphates and poly-phosphates to pyrophosphates and their crystallization. The decomposition mechanism was confirmed when using the X-ray diffraction patterns of the compound, thermally treated at several temperatures.

Sulphonated metal phthalocyanine complexes as redox indicators in micro titrations with cerium(IV) sulphate

Energy Technology Data Exchange (ETDEWEB)

Gowda, H S; Achar, B N [Mysore Univ. (India). Dept. of Chemistry

1980-01-01

Tetrasodium salts of copper(II) 4,4', 4'', 4'''-tetrasulphophthalocyanine 2-hydrate, nickel(II) 4,4', 4'', 4'''-tetrasulphophthalocyanine, nickel(II) 3,3', 3'', 3'''-tetrasulphophthalocyanine and cobalt(II) 4,4', 4'', 4'''-tetrasulphophthalocyanine 2-hydrate, and copper phthalocyanine trisulphonic acid are prepared in pure state. The molar absorptivity and formal redox potentials of the complexes are determined. The complexes are proposed as sensitive redox indicators in the micro determination of iron(II), arsenic(III), molybdenum(V), uranium(IV) and hydroquinone with 0.001-0.0005N cerium(IV) sulphate in sulphuric, hydrochloric and acetic acid media. They give sharp colour change from light turquoise blue to pale purple colour at the equivalence point. They have advantages over a few existing redox indicators.

Quantitation and identification of methanogens and sulphate reducers in Olkiluoto groundwater

International Nuclear Information System (INIS)

Bomberg, M.; Nyyssoenen, M.; Itaevaara, M.

2010-08-01

The GEOFUNC Project focuses on the microbiology connected to safety and risk assessment of the final disposal of high radioactive nuclear waste. Methanogenic archaea and sulphate reducing bacteria are significant groups of microorganisms in anaerobic environments, and are of crucial concern for the safe long term storage of nuclear waste in deep bedrock. The sulphate reducing bacteria are able to produce sulphide which may cause corrosion of the copper in the radioactive waste storage capsules. Methanogens, on the other hand, may produce quantities of methane from various organic carbon compounds, CO 2 and H 2 . Methane may both serve as carbon source for methanotrophic microbial groups, and may also cause mobilization of radionuclides, as a result of gas discharge through fractures in the bedrock. The transition zones between the sulphate rich and methane rich waters are locations for microbial processes where the methane may serve as carbon source for sulphate reducing bacteria, which in turn would produce corrosive sulphides. It has been estimated that only 1-10 % of all the microorganisms present in the environment can be isolated and cultivated. Uncultured microorganisms can be identified and their numbers in the environment quantified by identification of specific marker genes that are essential for their functions by use of molecular methods. Methanogens, for example, can be identified by their genes for methyl coenzyme M reductase (mcrA), which is an essential enzyme involved in the production of methane. The mcrA is specifically present only in methanogenic archaea. Sulphate reducers are identified by their dissimilatory sulphite reductase genes (dsrB), which are present in and essential for all microorganisms performing dissimilatory sulphate reducing. In the GEOFUNC project, a quantitative PCR method (qPCR) was developed for the detection of methanogens and sulphate reducers. This method is based on specific quantitative detection of marker genes

Alternative method of portable irradiation of manganese sulphate solution by an plutonium-beryllium source for manganese sulphate bath efficiency measurements; Metodo alternativo de irradiacao portatil da solucao de sulfato de manganes por uma fonte de plutonio-berilio para medicoes de eficiencia do banho de sulfato de manganes

Energy Technology Data Exchange (ETDEWEB)

Silva, Fellipe Souza da; Martins, Marcelo Marques; Pereira, Walsan Wagner, E-mail: fellipess@ird.gov.br [Instituto de Radioprotecao e Dosimetria (IRD/CNEN-RJ), Rio de Janeiro, RJ (Brazil)

2016-07-01

This study intends to create an alternative irradiation system from a Plutonium-Beryllium source for manganese sulphate solution using the Monte Carlo code. Thus seeking to eliminate the issue of institutes that do not have reactors or particle accelerators in its infrastructure, in order to optimize and provide independence for them to carry out efficiency measurements of MnSO{sub 4} solution in their own locality. The Monte Carlo simulations defined the technical features of this new system so that the solution reaches the maximum neutron capture by manganese in solution. (author)

Optimisation of the zinc sulphate turbidity test for the determination of immune status.

Science.gov (United States)

Hogan, I; Doherty, M; Fagan, J; Kennedy, E; Conneely, M; Crowe, B; Lorenz, I

2016-02-13

Failure of passive transfer of maternal immunity occurs in calves that fail to absorb sufficient immunoglobulins from ingested colostrum. The zinc sulphate turbidity test has been developed to test bovine neonates for this failure. The specificity of this test has been shown to be less than ideal. The objective was to examine how parameters of the zinc sulphate turbidity test may be manipulated in order to improve its diagnostic accuracy. One hundred and five blood samples were taken from calves of dairy cows receiving various rates of colostrum feeding. The zinc sulphate turbidity test was carried out multiple times on each sample, varying the solution strength, time of reaction and wavelength of light used and the results compared with those of a radial immunodiffusion test, which is the reference method for measuring immunoglobulin concentration in serum. Reducing the time over which the reaction occurs, or increasing the wavelength of light used to read the turbidity, resulted in decreased specificity without improving sensitivity. Increasing the concentration of the zinc sulphate solution used in the test was shown to improve the specificity without decreasing sensitivity. Examination of the cut-off points suggested that a lower cut-off point would improve the performance. British Veterinary Association.

THE ROLE OF PIPE AGEING IN COPPER CORROSION BY-PRODUCT RELEASE

Science.gov (United States)

The presence of sulphate, bicarbonate and orthophosphate can change the type of solid present in systems containing cupric ion or cupric hydroxide solids. In some cases, a short-term reduction in copper solubility is realized, but over longer periods of time formation of basic c...

Electrochemical Behavior of Pure Copper in Phosphate Buffer Solutions: A Comparison Between Micro- and Nano-Grained Copper

Science.gov (United States)

Imantalab, O.; Fattah-alhosseini, A.; Keshavarz, M. K.; Mazaheri, Y.

2016-02-01

In this work, electrochemical behavior of annealed (micro-) and nano-grained pure copper (fabricated by accumulative roll bonding process) in phosphate buffer solutions of various pH values ranging from 10.69 to 12.59 has been studied. Before any electrochemical measurements, evaluation of microstructure was obtained by optical microscope and transmission electron microscopy. To investigate the electrochemical behavior of the samples, the potentiodynamic polarization, Mott-Schottky analysis, and electrochemical impedance spectroscopy (EIS) were carried out. Potentiodynamic polarization plots and EIS measurements revealed that as a result of grain refinement, the passive behavior of the nano-grained sample was improved compared to that of annealed pure copper. Also, Mott-Schottky analysis indicated that the passive films behaved as p-type semiconductors and grain refinement did not change the semiconductor type of passive films.

Inhibition Effect of 1-Butyl-4-Methylpyridinium Tetrafluoroborate on the Corrosion of Copper in Phosphate Solutions

Directory of Open Access Journals (Sweden)

M. Scendo

2011-01-01

Full Text Available The influence of the concentration of 1-Butyl-4-methylpyridinium tetrafluoroborate (4MBPBF4 as ionic liquid (IL on the corrosion of copper in 0.5 M PO43− solutions of pH 2 and 4 was studied. The research involved electrochemical polarization method, and scanning electron microscopy (SEM technique. The results obtained showed that the inhibition efficiency of corrosion of copper increases with an increase in the concentration of 4MBPBF4 but decreases with increasing temperature. The thermodynamic functions of corrosion analysis and adsorptive behavior of 4MBPBF4 were carried out. During the test, the adsorption of the inhibitor on the copper surface in the phosphate solutions was found to obey the Langmuir adsorption isotherm and had a physical mechanism.

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

Science.gov (United States)

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.

Characterization of copper toxicity in letttuce seedlings

Energy Technology Data Exchange (ETDEWEB)

Mukherji, S; Gupta, B D

1972-01-01

Information on the effects of toxic concentration of cupric sulphate on the growth of lettuce (Lactuca sativa) seedlings is provided. Root growth is completely inhibited at 5 x 10/sup -2/ M and germination stops altogether at 10/sup -1/ M. The relative inhibition of root growth is stronger than that of hypocotyl growth. Various metabolites and hormones are partially capable of relieving copper inhibition. Catalase, peroxidase and IAA-oxidase activity shows increments directly proportional to the concentration of copper. It is obvious that growth is inversely proportional to enzyme activity. The increased level of these enzymes is probably due to an accelerated protein synthesis.

Sulphate, more than a nutrient, protects the microalga Chlamydomonas moewusii from cadmium toxicity

Energy Technology Data Exchange (ETDEWEB)

Mera, Roi; Torres, Enrique, E-mail: torres@udc.es; Abalde, Julio

2014-03-01

Highlights: • Sulphate effect on cadmium toxicity in the microalga Chlamydomonas moewusii Gerloff. • Cadmium increases the sulphur requirements in Chlamydomonas moewusii. • Kinetic coefficients for sulphate utilization and cadmium effect on them. • Sulphate and cadmium influence on the biosynthesis of low-molecular mass thiols. • Cadmium toxicity reduction by sulphate due to higher biosynthesis of thiols. - Abstract: Sulphur is an essential macroelement that plays important roles in living organisms. The thiol rich sulphur compounds, such as cysteine, γ-Glu–Cys, glutathione and phytochelatins participate in the tolerance mechanisms against cadmium toxicity. Plants, algae, yeasts and most prokaryotes cover their demand for reduced sulphur by reduction of inorganic sulphate. The aim of this study was to investigate, using a bifactorial experimental design, the effect of different sulphate concentrations in the nutrient solution on cadmium toxicity in the freshwater microalga Chlamydomonas moewusii. Cell growth, kinetic parameters of sulphate utilization and intracellular concentrations of low-molecular mass thiol compounds were determined. A mathematical model to describe the growth of this microalga based on the effects of sulphate and cadmium was obtained. An ANOVA revealed an interaction between them, 16% of the effect sizes was explained by this interaction. A higher amount of sulphate in the culture medium allowed a higher cadmium tolerance due to an increase in the thiol compound biosynthesis. The amount of low-molecular mass thiol compounds, mainly phytochelatins, synthesized by this microalga was significantly dependent on the sulphate and cadmium concentrations; the higher phytochelatin content was obtained in cultures with 4 mg Cd/L and 1 mM sulphate. The maximum EC{sub 50} value (based on nominal cadmium concentration) reached for this microalga was 4.46 ± 0.42 mg Cd/L when the sulphate concentration added to the culture medium was also 1 m

Preliminary Data on the In Vitro Effect of Copper-Based Compounds on Aerobic Bacterial Microflora Isolated from Sheep Footrot

Directory of Open Access Journals (Sweden)

Flore CHIRILĂ

2018-05-01

The results demonstrated that 7 of the samples (58.33 % are sensitive to the product I, 6 samples (50% to the product III, 4 samples (33.33 % to the product 2 and the 0.5% Copper sulphate solution only has a bacteriostatic effect. In comparison to the two antibiotics, 9 samples (75 % are sensitive to enrofloxacin and only 5 samples (41.66 % to oxytetracycline. Regarding the associations of microorganisms in the samples with resistance, we have found that these are represented by the most common germs of genus Bacillus, Corynebacterium and Gram negative bacteria, and rarer associations with Micrococcus and Staphylococcus.

Optimizing the recovery of copper from electroplating rinse bath solution by hollow fiber membrane.

Science.gov (United States)

Oskay, Kürşad Oğuz; Kul, Mehmet

2015-01-01

This study aimed to recover and remove copper from industrial model wastewater solution by non-dispersive solvent extraction (NDSX). Two mathematical models were developed to simulate the performance of an integrated extraction-stripping process, based on the use of hollow fiber contactors using the response surface method. The models allow one to predict the time dependent efficiencies of the two phases involved in individual extraction or stripping processes. The optimal recovery efficiency parameters were determined as 227 g/L of H2SO4 concentration, 1.22 feed/strip ratio, 450 mL/min flow rate (115.9 cm/min. flow velocity) and 15 volume % LIX 84-I concentration in 270 min by central composite design (CCD). At these optimum conditions, the experimental value of recovery efficiency was 95.88%, which was in close agreement with the 97.75% efficiency value predicted by the model. At the end of the process, almost all the copper in the model wastewater solution was removed and recovered as CuSO4.5H2O salt, which can be reused in the copper electroplating industry.

Production of ferric sulphate from pyrite by thiobacillus ferrooxidans. Application to uranium ore leaching

International Nuclear Information System (INIS)

Rouas, C.

1988-12-01

A process for uranium extraction by oxidizing solutions of ferric sulphate produced by T. ferrooxidans from pyrite is developed. A new counting method specific of T. ferrooxidans is designed. An uranium resistant wild strain, with oxidizing properties as high as the strain ATCC 19859, is isolated. Optimal conditions for ferric sulphate production from pyrite are defined (pH 1.8, density of the medium 1.2%, pyrite granulometry [fr

Corrosion control of copper in 3.5 wt.% NaCl Solution by Domperidone: Experimental and Theoretical Study

International Nuclear Information System (INIS)

Wang, Dan; Xiang, Bin; Liang, Yuanpeng; Song, Shan; Liu, Chao

2014-01-01

Highlights: • Domperidone has good inhibition effect for copper in 3.5 wt.% NaCl solution. • Domperidone acts as an anodic type inhibitor. • The SEM and AFM analyses support the weight loss, polarization, and EIS data. • Molecular dynamics (MD) method simulates the adsorption model of domperidone on Cu surface. • The adsorption of domperidone on copper surface obeys Langmuir adsorption isotherm. - Abstract: Inhibition of copper corrosion in 3.5 wt.% NaCl solution by domperidone was investigated by weight loss, potentiodynamic polarization and electrochemical impedance spectroscopy (EIS). The experimental results revealed that domperidone was an anodic inhibitor with a maximum achievable inhibition efficiency of 94.2%. The results of SEM and AFM studies further confirmed the inhibition action of domperidone. Quantum chemical calculation and the molecular dynamics (MD) simulation showed that the domperidone molecule could be adsorbed on copper surface through the imidazolidinone ring, benzene ring and N atom of hexaheterocyclic. Adsorption of domperidone was found to follow the Langmuir adsorption isotherm

Crystallisation of mixtures of ammonium nitrate, ammonium sulphate and soot

NARCIS (Netherlands)

Dougle, P.G.; Veefkind, J.P.; Brink, H.M. ten

1998-01-01

Crystallisation of laboratory aerosols of ammonium nitrate and of internal mixtures of this salt with ammonium sulphate were investigated using humidity controlled nephelometry. The aerosol was produced via nebulizing of solutions and then dried to 25% RH, which is a realistic minimum value for

Flotation of traces of silver and copper(II) ions with a methyl cellosolve solution of dithizone.

Science.gov (United States)

Hiraide, M; Mizuike, A

1975-06-01

Microgram quantities of silver and copper(II) ions in aqueous solutions are collected on dithizone precipitates, which are then floated with the aid of small nitrogen bubbles. This separation technique has been successfully applied to the atomic-absorption spectrophotometric determination of down to a tenth ppm of silver and copper in high-purity lead and zinc metals.

Corrosion behaviour of Alloy 800 in high temperature aqueous solutions: Electrochemical studies

International Nuclear Information System (INIS)

Olmedo, A.M.; Villegas, M.; Alvarez, M.G.

1996-01-01

The anodic behaviour and passivity breakdown of Alloy 800 in aqueous solutions of sodium chloride, sodium sulphate and sodium bicarbonate were studied by electrochemical techniques in the temperature range from 60 C to 280 C. The pitting resistance and pitting morphology of the alloy in chloride plus sulphate and chloride plus bicarbonate mixtures, at 60 C and 280 C, were also examined. Increasing bicarbonate or sulphate additions to chloride solutions shift the characteristic pitting potential of Alloy 800 to higher values, both at low and high temperatures. Changes in pitting morphology were observed in sulphate containing solutions while the morphology of the attack found in bicarbonate containing solutions was similar to that in pure chloride solutions. Finally, no localized or substantial generalized corrosion was detected in pure sulphate or bicarbonate solutions at any temperature. (orig.)

Grape berry bacterial inhibition by different copper fungicides

Directory of Open Access Journals (Sweden)

Martins Guilherme

2016-01-01

Full Text Available Copper fungicides are widely used in viticulture. Due to its large spectrum of action, copper provides an efficient control over a great number of vine pathogens. Previous studies showed that, high levels of cupric residues can impact grape-berry microbiota, in terms of the size and population structure, reducing the diversity and the abundance. Due to the importance of grape-berry bacterial in crop health, and the potential impact of copper fungicides over the microbiota, we determined Minimum Inhibitory Concentration (MIC of different copper formulations for bacterial species isolated from grape berries. We study the Minimum Inhibitory Concentration (MIC of different copper formulations (copper sulphate (CuSO4 pure, Bordeaux mixture (CuSO4 + Ca(OH2, copper oxide (Cu2O, copper hydroxide (Cu(OH2 over 92 bacterial strains isolated from grape berries in different stages of the ripening process. The results of MIC measurements revealed that the different copper formulations have a variable inhibitory effect and among the different isolates, some species are the most resistant to all copper formulations than others. This study confirm that usage of cupric phytosanitary products should be reasonable independently of the farming system; they also provide evidence of the importance of the choice of which copper formulations are to be used regarding their impact on the grape berry bacterial microbiota.

Effects of pulsing solution, packaging material and passive ...

African Journals Online (AJOL)

The experiment consisted of four pulsing solutions (silver thiosulfate + Chrysal clear solution (RVB), silver thiosulfate + 8-hydroxyquinoline sulphate, silver thiosulfate + Chrysal clear solution + hydroxyquinoline sulphate and H2O), two packaging types (cardboard box and box with polyethylene bag) and four storage period ...

Effects of copper-based compounds, antibiotics and a plant activator on population sizes and spread of Clavibacter michiganensis subsp. michiganensis in greenhouse tomato seedlings

OpenAIRE

Milijašević Svetlana; Todorović Biljana; Potočnik Ivana; Rekanović Emil; Stepanović Miloš

2009-01-01

Three copper-based compounds (copper hydroxide, copper oxychloride, copper sulphate), two antibiotics (streptomycin and kasugamycin) and a plant activator (ASM) significantly reduced population sizes and spread of C. michiganensis subsp. michiganensis among tomato seedlings in the greenhouse. Streptomycin had the best effect in reducing pathogen population size in all sampling regions. Moreover, this antibiotic completely stopped the spread of C. michiganensis subsp. michiganensis in the regi...

Solvent extraction of Cu, Mo, V, and U from leach solutions of copper ore and flotation tailings

International Nuclear Information System (INIS)

Smolinski, Tomasz; Wawszczak, Danuta; Deptula, Andrzej; Lada, Wieslawa; Olczak, Tadeusz; Rogowski, Marcin; Pyszynska, Marta; Chmielewski, Andrzej Grzegorz

2017-01-01

Flotation tailings from copper production are deposits of copper and other valuable metals, such as Mo, V and U. New hydrometallurgical technologies are more economical and open up new possibilities for metal recovery. This work presents results of the study on the extraction of copper by mixed extractant consisting p-toluidine dissolved in toluene. The possibility of simultaneous liquid-liquid extraction of molybdenum and vanadium was examined. D2EHPA solutions was used as extractant, and recovery of individual elements compared for the representative samples of ore and copper flotation tailings. Radiometric methods were applied for process optimization. (author)

Solvent extraction of Cu, Mo, V, and U from leach solutions of copper ore and flotation tailings.

Science.gov (United States)

Smolinski, Tomasz; Wawszczak, Danuta; Deptula, Andrzej; Lada, Wieslawa; Olczak, Tadeusz; Rogowski, Marcin; Pyszynska, Marta; Chmielewski, Andrzej Grzegorz

2017-01-01

Flotation tailings from copper production are deposits of copper and other valuable metals, such as Mo, V and U. New hydrometallurgical technologies are more economical and open up new possibilities for metal recovery. This work presents results of the study on the extraction of copper by mixed extractant consisting p -toluidine dissolved in toluene. The possibility of simultaneous liquid-liquid extraction of molybdenum and vanadium was examined. D2EHPA solutions was used as extractant, and recovery of individual elements compared for the representative samples of ore and copper flotation tailings. Radiometric methods were applied for process optimization.

Asymptotically exact solution of a local copper-oxide model

International Nuclear Information System (INIS)

Zhang Guangming; Yu Lu.

1994-03-01

We present an asymptotically exact solution of a local copper-oxide model abstracted from the multi-band models. The phase diagram is obtained through the renormalization-group analysis of the partition function. In the strong coupling regime, we find an exactly solved line, which crosses the quantum critical point of the mixed valence regime separating two different Fermi-liquid (FL) phases. At this critical point, a many-particle resonance is formed near the chemical potential, and a marginal-FL spectrum can be derived for the spin and charge susceptibilities. (author). 15 refs, 1 fig

Dependency of the band gap of electrodeposited Copper oxide thin films on the concentration of copper sulfate (CuSO4.5H2O) and pH in bath solution for photovoltaic applications

KAUST Repository

Islam, Md. Anisul

2016-03-10

In this study, Copper oxide thin films were deposited on copper plate by electrodeposition process in an electrolytic bath containing CuSO4.5H2O, 3M lactic acid and NaOH. Copper oxide films were electrodeposited at different pH and different concentration of CuSO4.5H2O and the optical band gap was determined from their absorption spectrum which was obtained from UV-Vis absorption spectroscopy. It was found that copper oxide films which were deposited at low concentration of CuSO4.5H2O have higher band gap than those deposited at higher bath concentration. The band gap of copper oxide films also significantly changes with pH of the bath solution. It was also observed that with the increase of the pH of bath solution band gap of copper oxide film decreased. © 2015 IEEE.

Sulphate reduction in the Aespoe HRL tunnel

International Nuclear Information System (INIS)

Gustafson, G.; Pedersen, K.; Tullborg, E.L.; Wallin, B.; Wikberg, P.

1995-12-01

Evidence and indications of sulphate reduction based on geological, hydrogeological, groundwater, isotope and microbial data gathered in and around the Aespoe Hard Rock Laboratory tunnel have been evaluated. This integrated investigation showed that sulphate reduction had taken place in the past but is most likely also an ongoing process. Anaerobic sulphate-reducing bacteria can live in marine sediments, in the tunnel sections under the sea and in deep groundwaters, since there is no access to oxygen. The sulphate-reducing bacteria seem to thrive when the Cl - concentration of the groundwater is 4000-6000 mg/l. Sulphate reduction is an in situ process but the resulting hydrogen-sulphide rich water can be transported to other locations. A more vigorous sulphate reduction takes place when the organic content in the groundwater is high (>10 mg/l DOC) which is the case in the sediments and in the groundwaters under the sea. Some bacteria use hydrogen as an electron donor instead of organic carbon and can therefore live in deep environments where access to organic material is limited. The sulphate-reducing bacteria seem to adapt to changing flow situations caused by the tunnel construction relatively fast. Sulphate reduction seems to have occurred and will probably occur where conditions are favourable for the sulphate-reducing bacteria such as anaerobic brackish groundwater with dissolved sulphate and organic carbon or hydrogen. 59 refs, 37 figs, 6 tabs

Yttrium 3-(4-nitrophenyl)-2-propenoate used as inhibitor against copper alloy corrosion in 0.1 M NaCl solution

International Nuclear Information System (INIS)

Nam, Nguyen Dang; Thang, Vo Quoc; Hoai, Nguyen To; Hien, Pham Van

2016-01-01

Highlights: • Yttrium 3-(4-nitrophenyl)-2-propenoate has been studied as an effective corrosion inhibitor for copper. • A high inhibition performance is attributed to the forming protective inhibiting deposits. • Yttrium 3-(4-nitrophenyl)-2-propenoate mitigates corrosion by promoting random distribution of minor anodes. - Abstract: Yttrium 3-(4-nitrophenyl)-2-propenoate has been studied as an effective corrosion inhibitor for copper alloy in 0.1 M chloride solution. The results show that the surface of copper alloy coupons exposed to solutions containing 0.45 mM yttrium 3-(4-nitrophenyl)-2-propenoate had no signs of corrosion attack due to protective film formation, whereas the surface of copper alloy coupons exposed to non-inhibitor and lower concentrations of yttrium 3-(4-nitrophenyl)-2-propenoate containing solutions were severely corroded. A high inhibition performance is attributed to the forming protective inhibiting deposits that slow down the electrochemical corrosion reactions and mitigate corrosion by promoting random distribution of minor anodes.

Investigation of the immobilisation/mobilisation of nickel, copper ...

African Journals Online (AJOL)

DRINIE

nitrate, manganese hydroxides, iron hydroxides, sulphate and carbon dioxide). ... standard solution contained (g·l-1 dH2O): ferrous ammonium sulphate, 39.21; ferric ... (AAS) with a nitrous oxide-acetylene flame, to minimise chemical interferences, was ... The synthetic refuse used facilitated the production of volatile fatty ...

Structure of sodium alkyl sulphate micelles

International Nuclear Information System (INIS)

Vass, Sz.

1990-05-01

Micellar aggregation numbers of aggregated sodium octyl, decyl, dodecyl and tetradecyl sulphate molecules obtained from small-angle neutron scattering (SANS) measurements are reported. The surfactant concentration and solution temperature were varied systematically. A survey of the physical models and evaluation algorithms applied for SANS are presented. By utilizing a new least square fitting algorithm, the formation and annihilation parameters of orthopositronium in the micellar pseudophase and in the aqueous solvent is deduced by evaluating positron lifetime spectra measured by conventional technqiues. (R.P.) 157 refs.; 10 figs

Kinetic and Thermodynamic Studies on Adsorption of Sulphate from ...

African Journals Online (AJOL)

DELL USER

22, No. 1, 2017. 39. Kinetic and Thermodynamic Studies on Adsorption of Sulphate from Aqueous Solution by. Magnetite ... poison catalysts, and affect the .... C for 1 h in a stainless steel reactor placed in a furnace ... N2 gas for 30 min. 50 ml of ...... adsorption for designing and evaluating the ... is the equilibrium liquid-phase.

Acute Toxicity and the Effects of Copper Sulphate (CuSO4.5H2O on the Behavior of the Black Fish (Capoeta Fusca

Directory of Open Access Journals (Sweden)

Iman Zarei

2013-02-01

Full Text Available Background: The development of toxicity tests regarding toxic responses of different fish species could be more effectively used in predictive toxicology and risk assessment. In this study lethal concentrations (LC50-96 h values of copper sulphate; an important toxic industrial pollutant, on Capoeta fusca were determined. Behavioral changes at different concentrations of CuSO4 were determined for the C.fusca. Methods: The sample fishes were collected from Qanat in Birjand and were transported to the laboratory in polythene bags. The exposure time of fish to CuSO4 was 96 hours. Mortalities were recorded at 24, 48, 72, and 96 hours of exposure, and the dead fish were removed regularly from the test aquariums. Physicochemical parameters, such as dissolved oxygen, pH and Total hardness of aquaria were monitored daily. Results: The LC50 values for CuSO4 at 24, 48, 72, and 96 h of exposure, were 43.62, 12.6, 7.66, and 6.85 mg/L, respectively. The median LC50 value of CuSO4 for C.fusca was found to be 6.928 mg/L by EPA method and estimated to be 6.787 mg/L with SPSS statistical software. Conclusion: The mortality decreased with time, and most of the deaths occurred during the first 24 h. In addition, behavioural changes increased with increased concentration. This metal is an important constituent in industrial effluents discharged into freshwaters. The results obtained in this study clearly revealed the fact that it is necessary to control the use of a heavy metal such as copper.

Complex crystals formed in the aqueous solution of copper(I) iodide and sodium iodide

International Nuclear Information System (INIS)

Sugasaka, Kazuhiko; Fujii, Ayako

1977-01-01

Crystals of different crystal habits were separated from the copper(I) iodide and sodium iodide solution and the thermal changes of the composition of copper(I) iodide and sodium iodide complexes were studied by chemical analysis, thermal analysis and X-ray diffractometry. Granular and columnar crystals were determined to be copper(I) iodide and sodium iodide dihydrate by X-ray diffraction analysis, respectively. Needle crystal (A) which was separated from the solution at 25 0 C was assumed to be Na 2 CuI 3 .6H 2 O. (A) was stable in its appearance in the air, but the X-ray diffraction pattern of (A) changed. Needle crystal (B) which was recrystallized at 10 0 C from mother liquor after the separation of crystal (A) was assumed to be NaCuI 2 .4H 2 O. (B) was hygroscopic and decomposed to precipitate copper(I) iodide with moisture in the air. (A) and (B) were found to change by heating and or drying, respectively, as follows: Na 2 CuI 3 .6H 2 O → (-2H 2 O, 80 0 C) → 2NaI.2H 2 O + CuI → (-4H 2 O, 160 0 C) → 2NaI + CuI → (+1/2O 2 , 450 0 C) → 2NaI + CuO + 1/2I 2 , NaCuI 2 .4H 2 O → (-4H 2 O, Dried) → NaI + CuI. (auth.)

Chemically modified Moringa oleifera seed husks as low cost adsorbent for removal of copper from aqueous solution

Science.gov (United States)

Ghafar, Faridah; Mohtar, Aminullah; Sapawe, Norzahir; Hadi, Norulakmal Nor; Salleh, Marmy Roshaidah Mohd

2017-12-01

Moringa oleifera husks (MOH) are an agricultural byproduct that may have potential as adsorbent for removal of heavy metal ions in wastewater such as copper (Cu2+). The release of Cu2+ to the environment by the mining and electroplating industries cause a major problem because it is toxic and can cause liver and kidney problems. Hence, it is important to remove copper before the wastewater can be discharged to the environment. In order to increase the adsorption capacity, the MOH was chemically modified using citric acid. The raw and modified MOH were analyzed using Fourier Transform Infra-Red (FTIR) for identification of functional groups present at the adsorbent surface. The adsorption study was carried out using the batch technique in water bath shaker investigating different parameters; adsorbent dosage (30 - 70 g/L), initial concentration of copper (30 - 150 mg/L), contact time (2 - 90 min), temperature (27 - 60 °C) at constant agitation of 100 rpm. The concentrations of copper in aqueous solution before and after the adsorption process was analyzed using Atomic Absorption Spectrum (AAS). The highest percentage removal of copper was found at 10g/L of adsorbent dosage with 30 mg/L of initial concentration and temperature 30 °C. It was also observed that the adsorption of copper by MOH was approaching to equilibrium at 60 min of reaction time. From the FTIR analysis, it was found that the MOH contains hydroxyl, carboxyl and amine groups. The high adsorption capacity of modified MOH to remove copper from aqueous solution makes it preferable and attractive alternative to commercial adsorbent.

Separation of copper-64 from copper phthalocyanine

International Nuclear Information System (INIS)

Battaglin, R.I.M.

1979-01-01

The separation of copper-64 from irradiated copper phthalocyanine by Szilard-Chalmers effect is studied. Two methods of separation are used: one of them is based on the dissolution of the irradiated dry compound in concentrated sulfuric acid following its precipitation in water. In the other one the compound is irradiated with water in paste form following treatment with water and hydrochloric acid. The influence of the crystal form of the copper phthalocyanine on the separation yield of copper-64 is shown. Preliminary tests using the ionic exchange technique for purification and changing of copper-64 sulfate to chloride form are carried out. The specific activity using the spectrophotometric technique, after the determination of the copper concentration in solution of copper-64, is calculated. (Author) [pt

Risk minimisation of FGD gypsum leachates by incorporation of aluminium sulphate

Energy Technology Data Exchange (ETDEWEB)

Alvarez-Ayuso, E. [Department of Environmental Geology, Institute of Earth Sciences ' Jaume Almera' (CSIC), C/ Lluis Sole i Sabaris, s/n, 08028 Barcelona (Spain); Department of Environmental Geochemistry, IRNASA, CSIC, Apto. 257, 37071 Salamanca (Spain)], E-mail: ealvarez@ija.csic.es; Querol, X. [Department of Environmental Geology, Institute of Earth Sciences ' Jaume Almera' (CSIC), C/ Lluis Sole i Sabaris, s/n, 08028 Barcelona (Spain); Ballesteros, J.C.; Gimenez, A. [Endesa Generacion, S.A., C/ Ribera de Loira, 60, 28042 Madrid (Spain)

2008-11-15

The incorporation of aluminium sulphate to (flue gas desulphurisation) FGD gypsum before its disposal was investigated as a way to minimise the risk supposed by the high fluoride content of its leachates. Using a bath method the kinetic and equilibrium processes of fluoride removal by aluminium sulphate were studied at fluoride/aluminium molar concentration (F/Al) ratios in the range 1.75 10{sup -2}-1.75 under the pH conditions (about 6.5) of FGD gypsum leachates. It was found that fluoride removal was a very fast process at any of the (F/Al) ratios subject of study, with equilibrium attained within the first 15 min of interaction. High decreases in solution fluoride concentrations (50-80%) were found at the equilibrium state. The use of aluminium sulphate in the stabilization of FGD gypsum proved to greatly decrease its fluoride leachable content (in the range 20-90% for aluminium sulphate doses of 0.1-5%, as determined by the European standard EN 12457-4). Such fluoride leaching minimisation assures the characterization of this by-product as a waste acceptable at landfills for non-hazardous wastes according to the Council Decision 2003/33/EC on waste disposal. Furthermore, as derived from column leaching studies, the proposed stabilization system showed to be highly effective in simulated conditions of disposal, displaying fluoride leaching reduction values about 55 and 80% for aluminium sulphate added amounts of 1 and 2%, respectively.

Measured Copper Toxicity to Cnesterodon decemmaculatus (Pisces: Poeciliidae and Predicted by Biotic Ligand Model in Pilcomayo River Water: A Step for a Cross-Fish-Species Extrapolation

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María Victoria Casares

2012-01-01

Full Text Available In order to determine copper toxicity (LC50 to a local species (Cnesterodon decemmaculatus in the South American Pilcomayo River water and evaluate a cross-fish-species extrapolation of Biotic Ligand Model, a 96 h acute copper toxicity test was performed. The dissolved copper concentrations tested were 0.05, 0.19, 0.39, 0.61, 0.73, 1.01, and 1.42 mg Cu L-1. The 96 h Cu LC50 calculated was 0.655 mg L-1 (0.823-0.488. 96-h Cu LC50 predicted by BLM for Pimephales promelas was 0.722 mg L-1. Analysis of the inter-seasonal variation of the main water quality parameters indicates that a higher protective effect of calcium, magnesium, sodium, sulphate, and chloride is expected during the dry season. The very high load of total suspended solids in this river might be a key factor in determining copper distribution between solid and solution phases. A cross-fish-species extrapolation of copper BLM is valid within the water quality parameters and experimental conditions of this toxicity test.

Removal of Copper ions from aqueous solutions using polymer derivations of poly (styrene-alt-maleic anhydride

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Naser Samadi

2017-06-01

Full Text Available In this study chelating resins have been considered to be suitable materials for the recovery of Copper (II ions in water treatments. Furthermore, these modified resins were reacted with 1,2-diaminoethane in the presence of ultrasonic irradiation for the preparation of a tridimensional chelating resin on the Nano scale for the recovery of Copper (II ions from aqueous solutions. This method which is used for removing and determining Copper (II ions using copolymers derived resins of poly (styrene-alternative-maleic anhydride (SMA and atomic absorption spectroscopy. The method is simple, sensitive, inexpensive and fast. The various parameters such as pH, contact time, concentrations of metal ions, mass of resin, and agitation speed were investigated on adsorption effect. The adsorption behavior of Copper (II ions were investigated by the synthesis of chelating resins at various pHs. The prepared resins showed a good tendency for removing the selected metal ions from aqueous solution, even at an acidic pH. Also, the prepared resins were examined for the removal of Copper (II ions from real samples such as industrial wastewater and were shown to be very efficient at adsorption in the cases of Copper (II ions. The pseudo-first-order, pseudo-second-order, and intra-particle diffusion kinetics equations were used for modeling of adsorption data and it was shown that pseudo-second-order kinetic equation could best describe the adsorption kinetics. The intra-particle diffusion study revealed that external diffusion might be involved in this case. The resins were characterized by Fourier transform infrared spectroscopy, scanning electron microscopy, and X-ray diffraction analysis.

Flotation of copper-bearing shale in solutions of inorganic salts and organic reagents

OpenAIRE

Ratajczak Tomasz

2017-01-01

Flotation data on copper-bearing shale in aqueous solutions of inorganic electrolytes (NaCl, Na2SO4, KPF6, NH4Cl) and organic reagents (ethylamine, propylamine) as frothers were presented and discussed. The relationships between shale flotation, surface tension of aqueous solution and foam height during bubbling with air in the flotation system were presented. It has been found that flotation of shale in the presence of inorganic salts the yield was directly proportional to the surface tensio...

Control strategies for bovine dermatophilosis with particular ...

African Journals Online (AJOL)

The various control strategies for Dermatophilosis are discussed in this paper. Recommendations for control of Dermatophilosis in Nigeria on short term include ecto-parasite control by regular use of insecticide/acaricide in dips with added 0.03% copper sulphate or 1% solution of alum (potassium aluminium sulphate) ...

Mineralogical Study of a Biologically-Based Treatment System That Removes Arsenic, Zinc and Copper from Landfill Leachate

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Maryam Khoshnoodi

2013-12-01

Full Text Available Mineralogical characterization by X-ray diffraction (XRD and a high throughput automated quantitative evaluation of minerals by scanning electron microscopy (QEMSCAN was conducted on samples from a sulphate-reducing biochemical reactor (BCR treating high concentrations of metals (As, Zn, Cu in smelter waste landfill seepage. The samples were also subjected to energy dispersive X-ray (EDX analysis of specific particles. The bulk analysis results revealed that the samples consisted mainly of silicate and carbonate minerals. More detailed phase analysis indicated four different classes: zinc-arsenic sulphosalts/sulphates, zinc-arsenic oxides, zinc phosphates and zinc-lead sulphosalts/sulphates. This suggests that sulphates and sulphides are the predominant types of Zn and As minerals formed in the BCR. Sphalerite (ZnS was a common mineral observed in many of the samples. In addition, X-ray point analysis showed evidence of As and Zn coating around feldspar and amphibole particles. The presence of arsenic-zinc-iron, with or without cadmium particles, indicated arsenopyrite minerals. Copper-iron-sulphide particles suggested chalcopyrite (CuFeS2 and tennantite (Cu,Fe12As4S13. Microbial communities found in each sample were correlated with metal content to describe taxonomic groups associated with high-metal samples. The research results highlight mineral grains that were present or formed at the site that might be the predominant forms of immobilized arsenic, zinc and copper.

Radioprotective effects of dextran sulphate in mice

International Nuclear Information System (INIS)

Vacek, A.; Bartonickova, A.; Rotkovska, D.; Palyga, G.F.; Zhukova, N.A.

1981-01-01

Influence of a single i.p. injection of dextran sulphate on radiosensitivity of mice was investigated. The administration of dextran sulphate 24, 48 and 72 hours prior to irradiation increased formation of endogenous colonies of the hemopoietic tissue on the surface of the spleen. DRF calculated from an equieffective exposure for 5 colonies was 1.96 when dextran sulphate was administered 24 hours before irradiation, and 2.25 when dextran sulphate was administered 72 hours before irradiation. The radioprotective effects of dextran sulphate were manifested also in the survival of animals exposed to lethal doses of short-termed as well as long-termed gamma radiation. (orig.) [de

Preparation methods of copper-ferrocyanide functionalized magnetic nanoparticles for selective removal of cesium in aqueous solution

Energy Technology Data Exchange (ETDEWEB)

Hee-Man Yang; Kune Woo Lee; Bum-Kyoung Seo; Jei Kwon Moon [KAERI, Daejeon (Korea, Republic of)

2013-07-01

Copper ferrocyanide functionalized magnetite nanoparticles (Cu-FC-MNPs) were successfully synthesized by the immobilization of copper and ferrocyanide on the surface of [1-(2 amino-ethyl)-3-aminopropyl] trimethoxysilane modified magnetite nanoparticles. A radioactive cesium (Cs) adsorption test was carried out to investigate the effectiveness of Cu-FC-MNPS for the removal of radioactive Cs. Furthermore, the Cu-FC-MNPs showed excellent separation ability by an external magnet in an aqueous solution. (authors)

Reuse of Partially Sulphated CFBC Ash as an SO2 Sorbent

Energy Technology Data Exchange (ETDEWEB)

Wu, Yinghai; Jia, Lufei; Anthony, E.J. [CanmetENERGY, 1 Haanel Drive, Ottawa, Ontario, K1A1M1 (Canada); Nobili, M.; Telesca, A. [Department of Environmental Engineering and Physics, University of Basilicata, Viale dell' Ateneo, Lucano 10, 85100 Potenza (Italy); Montagnaro, F. [Department of Chemistry, University of Naples ' Federico II' , Monte Sant' Angelo, 80126 Naples (Italy)

2010-06-15

Ashes produced from fluidized bed combustors (FBC) burning high-sulphur fuels often contain 20-30 % unreacted CaO because of the limestone added to remove SO2 in situ. This paper presents the results from experiments into reactivating partially sulphated FBC ash (both bed ash and fly ash) with liquid water, steam and sodium carbonate. The water- or steam-hydrated ashes were subsequently re-sulphated in a thermogravimetric analyzer (TGA) with simulated flue gas. The TGA results show that, while liquid water and steam successfully hydrate and reactivate the unreacted CaO in the bed ash, the treated ashes sulphated to widely different extents. Attempts to reactivate fly ash with hydration failed, although fly ash by itself is extremely reactive. A pilot-scale mini-circulating FBC (CFBC) was also used to evaluate the results of reactivation on the bed ash by hydrating with liquid water and admixtures of inorganic salt (Na2CO3) in the form of either powder or solution. When the treated ash was re-injected into the combustor with the fuel, the effect on SO2 removal efficiency was negligible if Na2CO3 was added as powder. Doping with aqueous solution resulted in enhanced SO2 removal; however, the extent was lower than the level achieved if only water hydration was employed. Increasing the amount of water (from 10% to 30%) to reactivate the ash did not improve the sulphur capture capacity in the mini-CFBC. Overall, this study suggests that the most practical way for re-use of the partially sulphated bed ash as a sulphur sorbent is reactivation by water. A proposal for utilization of the fly ash in an economically reasonable way is also discussed.

Electrochemical removal of copper ions from dilute solutions using packed bed electrode. Part І

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I.A. Khattab

2013-06-01

Full Text Available Removal of some hazardous waste like copper from effluent streams has an industrial importance. In this field, this paper is directed towards electrochemical removal of copper ions from sulfate solution using packed bed electrode. The cathode packing is in static mode, consisted of graphite particles, with mean particle size equal to 0.125 cm. The high surface area of this cell is expected to give high current efficiency and removal percent. The effect of current density and liquid flow rate were tested. Experimental results obtained indicate that the efficiencies are in direct proportional with current density while inversely proportional with liquid flow rate. It was observed that, using this cell was effective in reducing copper concentration to less than 4 mg/l with R.E of 96.2% during 30 min electrolysis time.

Study of the sulphate expansion phenomenon in concrete: behaviour of the cemented radioactive wastes containing sulphate

International Nuclear Information System (INIS)

Li, Guanshu

1994-01-01

Sulphate attack is one of the major degradation processes of concrete. It is especially important in storing cemented radioactive wastes containing sulphate. In this thesis, we have thoroughly investigated the degradation mechanisms of cemented radioactive wastes by sulphate. The CaO-Al 2 O 3 -SO 3 -H 2 O systems with and without alkalis are studied. For the system without alkalis, experimental results show that it is the formation of a secondary ettringite under external water supply by steric effect that causes the expansion. For the system with alkalis, the ettringite does not appear while a new mineral called 'U', a sodium-substituted AFm phase is detected. This phase is shown to be responsible for the expansion and destruction of the specimens. The conditions for the formation, the product of solubility and many means of its synthesis are discussed, and a complete list of the inter-reticular distances file is given. The behaviour of the different types of cemented wastes containing sulphate are then studied with a special focus on the U phase on entity which was heretofore very little understood. The following three hypothetical mechanisms of sulphate expansion are proposed: the formation of the secondary U phase, the transformation of the U phase to the ettringite and the topochemical hydration of thenardite into mirabilite. Experiments on a simplified system have demonstrated clearly that the formation of the secondary U phase can induce enormous expansion by steric effect, this justifying the first assumption. Simulation by the mass and volume balances is carried out thereafter and enables us to estimate the expansion induced by the formation of the secondary U phase in the cemented wastes. The second assumption is also well verified by a series of leaching tests in different solutions on mixtures containing the U phase. On the basis of the analysis of the specimens under leaching, it has been assumed that the expansion is associated with the

Reuse of partially sulphated CFBC ash as an SO{sub 2} sorbent

Energy Technology Data Exchange (ETDEWEB)

Wu, Y.; Jia, L.; Anthony, E.J. [Natural Resources Canada, Ottawa, ON (Canada). CANMET Energy; Nobili, M.; Telesca, A. [Basilicata Univ., Potenza (Italy). Dept. of Environmental Engineering and Physics; Montagnaro, F. [Naples Univ., Naples (Italy). Dept. of Chemistry

2010-06-15

Ash produced from circulating fluidized bed combustion (CFBC) boilers typically contains large amounts of unreacted calcium oxide (CaO) when limestone is added into the combustor for in situ removal of sulphur dioxide (SO{sub 2}). This paper reported on a study that evaluated the reactivation of partially sulphated ash obtained from an industrial circulating fluidized bed combustion (CFBC) boiler by hydration with liquid water and steam. A pilot-scale mini-CFBC was used to evaluate the results of reactivation on the bed ash by hydrating with liquid water and admixtures of sodium carbonate (Na{sub 2}CO{sub 3}) in solution or as powder. Re-sulphation tests on the hydrated samples were performed in a Cahn 1000 thermogravimetric analyzer (TGA) at 850 degrees C for 90 minutes in a simulated flue gas environment with sulphur dioxide (SO{sub 2}) concentration at 5000 ppm. Re-sulphation was carried out on unhydrated ash at the same conditions used in the baseline test. The TGA results showed that although liquid water and steam successfully hydrate and reactivate the unreacted CaO in the bed ash, the treated ashes sulphated to widely different extents. Attempts to reactivate fly ash with hydration failed, but the fly ash by itself was extremely reactive. When the treated ash was re-injected into the combustor with the fuel, the effect on SO{sub 2} removal efficiency was negligible if Na{sub 2}CO{sub 3} was added as powder. Doping with aqueous solution improved SO{sub 2} removal, but to a lesser extent than if only water hydration was used. Increasing the amount of water to reactivate the ash did not improve the sulphur capture capacity in the mini-CFBC. It was concluded that reactivation by water is the most practical way to reuse the partially sulphated bed ash as a sulphur sorbent. 21 refs., 7 tabs., 3 figs.

Electrodeposition of white copper-tin alloys from alkaline cyanide solutions

International Nuclear Information System (INIS)

Purwadaria, H.S.; Zainal Arifin Ahmad

2007-01-01

Electrodeposition of white copper-tin alloys (including with mir alloys) has been done onto planar mild steel substrates from alkaline cyanide solutions at 65 degree C. The chemical composition of the coating is influenced by plating bath composition and current density. White mir alloy can be produced from the test solution containing 10 g/l CuCN 2 ,45 g/l Na 2 SnO 3 , 25 g/l NaCN, and 12 g/l NaOH at current density about 5 mA/cm?2. The local compositions of the coating cross section were analyzed using EDX installed in a FESEM operated at an accelerating voltage of 20 kV. The phases formed during co-deposition process were identified using XRD at 25 mA current and 35 kV voltage. (Author)

Effect of fly ash content towards Sulphate resistance of oil palm shell lightweight aggregate concrete

Science.gov (United States)

Muthusamy, K.; Fadzil, M. Y.; Nazrin Akmal, A. Z. Muhammad; Ahmad, S. Wan; Nur Azzimah, Z.; Hanafi, H. Mohd; Mohamad Hafizuddin, R.

2018-04-01

Both oil palm shell (OPS) and fly ash are by-product generated from the industries. Disposal of these by-product as wastes cause negative impact to the environment. The use of both oil palm shell and fly ash in concrete is seen as an economical solution for making green and denser concrete. The primary aim of this research is to determine the effects of FA utilization as sand replacement in oil palm shell lightweight aggregate concrete (OPS LWAC) towards sulphate resistance. Five concrete mixes containing fly ash as sand replacement namely 0%, 10%, 20%, 30% and 40% were prepared in these experimental work. All mixes were cast in form of cubes before subjected to sulphate solution for the period of 5 months. It was found that addition of 10% fly ash as sand replacement content resulted in better sulphate resistance of OPS LWAC. The occurrence of pozzolanic reaction due to the presence of FA in concrete has consumed the vulnerable Calcium hydroxide to be secondary C-S-H gel making the concrete denser and more durable.

Sulphate solubility and sulphate diffusion in oxide glasses: implications for the containment of sulphate-bearing nuclear wastes; Solubilite et cinetiques de diffusion des sulfates dans differents verres d'oxydes: application au conditionnement des dechets nucleaires sulfates

Energy Technology Data Exchange (ETDEWEB)

Lenoir, M.

2009-09-15

The thesis deals with sulphate solubility and sulphate diffusion in oxide glasses, in order to control sulphate incorporation and sulphate volatilization in nuclear waste glasses. It was conducted on simplified compositions, in the SiO{sub 2}-B{sub 2}O{sub 3}-R{sub 2}O (R = Li, Na, K, Cs), SiO{sub 2}-B{sub 2}O{sub 3}-BaO and V{sub 2}O{sub 5}-B{sub 2}O{sub 3}-BaO systems. These compositions allowed us to study the influence of the nature of network-modifying ions (Li{sup +}, Na{sup +}, K{sup +}, Cs{sup +} or Ba{sup 2+}) and also of former elements (Si, B, V), on structure and properties of glasses. Sulphate volatility is studied in sodium borosilicate melts using an innovative technique of sulphate quantitation with Raman spectroscopy. This technique is useful to obtain kinetic curves of sulphate volatilization. The establishment of a model to fit these curves leads to the determination of diffusion coefficients of sulphate. These diffusion coefficients can thus be compared to diffusion coefficients of other species, determined by other techniques and presented in the literature. They are also linked to diffusion coefficients in relation with the viscosity of the melts. Concerning sulphate solubility in glasses, it depends on glass composition and on the nature of sulphate incorporated. Sulphate incorporation in alkali borosilicate glasses leads to the formation of a sulphate layer floating on top of the melt. Sulphate incorporation in barium borosilicate and boro-vanadate glasses leads to the crystallization of sulphate species inside the vitreous matrix. Moreover, sulphate solubility is higher in these glasses than in alkali borosilicates. Finally, exchanges between cations present in glasses and cations present in the sulphate phase are also studied. (author)

Performance of Periwinkle Shell Ash Blended Cement Concrete Exposed to Magnesium Sulphate

Directory of Open Access Journals (Sweden)

Umoh A.A.

2013-01-01

Full Text Available The study examined the compressive strength of periwinkle shell ash (PSA blended cement concrete in magnesium sulphate medium. Specimens were prepared from designed characteristics strength of 25 MPa. The cement replacement with PSA ranged between 0 and 40% by volume. A total of 180 cube specimens were cast and cured in water. At 28 days curing, 45 specimens each were transferred into magnesium sulphate of 1%, 3%, and 5% solution, while others were continuously cured in water and tested at 62, 92, and 152 days. The results revealed a higher loss in compressive strength with the control mix, and that it increases with increased in MgSO4 concentration and exposure period, whereas, the attack on the PSA blended cement concrete was less and the least value recorded by 10% PSA content. Therefore, the study concluded that the optimum percentage replacement of cement with 10% PSA could mitigate magnesium sulphate attack.

Biotreatment of Cr(VI) contaminated waters by sulphate reducing bacteria fed with ethanol

International Nuclear Information System (INIS)

Pagnanelli, F.; Cruz Viggi, C.; Cibati, A.; Uccelletti, D.; Toro, L.; Palleschi, C.

2012-01-01

Highlights: ► Use of ethanol as electron donor for sulphate-reducing bacteria for the treatment of Cr(VI). ► Isolation of contribution in Cr removal (adsorption vs. bioprecipitation). ► Bioassessment of the process effectiveness by ecotoxicological in vivo tests using C. elegans. - Abstract: Biological treatment of Cr(VI) contaminated waters was performed in fixed bed reactors inoculated with SRB (sulphate-reducing bacteria) growing on ethanol. Treatment efficiency was evaluated by checking chemical abatement of Cr(VI) and by ecotoxicological tests using the nematode Caenorhabditis elegans. A preliminary comparison between ethanol and lactate was performed, denoting that using ethanol, the same values of final sulphate abatement were obtained. In addition ethanol showed to be a substrate more competitive than lactate in kinetic terms. Fixed bed column reactors were continuously fed with a solution containing sulphates (3 g L −1 ), ethanol (1.5 g L −1 ) and Cr(VI) (50 mg L −1 ). At steady state the column inoculated with SRB removed 65 ± 5% of sulphate and 95 ± 5% of chromium. Bioactive removal mechanisms predominated over biosorption. Diminution of Cr(VI) toxicity was assessed by using the nematode C. elegans as a test organism showing that the survival of nematodes was 20% in the presence of the untreated influent and raised up to 53% when the nematodes were exposed to the treated effluent.

Protection of copper surface with phytic acid against corrosion in chloride solution.

Science.gov (United States)

Peca, Dunja; Pihlar, Boris; Ingrid, Milošev

2014-01-01

Phytic acid (inositol hexaphosphate) was tested as a corrosion inhibitor for copper in 3% sodium chloride. Phytic acid is a natural compound derived from plants, it is not toxic and can be considered as a green inhibitor. Electrochemical methods of linear polarization and potentiodynamic polarization were used to study the electrochemical behaviour and evaluate the inhibition effectiveness. To obtain the optimal corrosion protection the following experimental conditions were investigated: effect of surface pre-treatment (abrasion and three procedures of surface roughening), pre-formation of the layer of phytic acid, time of immersion and concentration of phytic acid. To evaluate the surface pre-treatment procedures the surface roughness and contact angle were measured. Optimal conditions for formation of phytic layer were selected resulting in the inhibition effectiveness of nearly 80%. Morphology and composition of the layer were further studied by scanning electron microscopy, energy dispersive X-ray spectroscopy and X-ray photoelectron spectroscopy. The layer of phytic acid with thickness in the nanometer range homogeneously covers the copper surface. The obtained results show that this natural compound can be used as a mildly effective corrosion inhibitor for copper in chloride solution.

Copper and brass aged at open circuit potential in slightly alkaline solutions

International Nuclear Information System (INIS)

Procaccini, R.; Vazquez, M.; Cere, S.

2009-01-01

Surface oxide films were grown on 99.99% copper and brass (copper-zinc alloy, Cu77Zn21Al2) in 0.1 mol L -1 borax solution at open circuit potential and were characterized using various experimental techniques. The composition of the passive films formed in situ on the different materials was studied using differential reflectance spectroscopy. The thickness of the oxide layers on copper and brass was compared by chronopotentiometric curves and potentiodynamic reductions. The electrical properties of each oxide were analyzed by means of electrochemical impedance spectroscopy. Their influence on the oxygen reduction reaction was also investigated using voltammetry hydrodynamic tools such as the rotating disk electrode. The results show that the incorporation of Zn to Cu in brass changes the composition and the thickness of the surface film. The films grown on brass tend to be thicker but less resistive and Zn compounds incorporate to the film. This is supported by results from reflectance and impedance spectroscopy. The kinetics of oxygen reduction is strongly inhibited on oxidized electrodes, particularly in the case of brass. The global number of exchanged electrons remains close to four and seems to be independent of the presence of surface oxides.

Lead, zinc and copper fine powder with controlled size and shape

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Mahmoud A Rabah

2017-12-01

Full Text Available This study describes the preparation of lead, zinc and copper powders by hydrometallurgy from secondary resources. Chloride, sulphate and acetate salts of zinc, copper and lead were prepared. The powders were prepared by reducing the ionic species of these metals by hydrazine hydrate or ascorbic acid. The effect of addition of some water soluble polar organic solvents to the aqueous salt solutions on the morphology and particle size of the prepared powder was studied. Findings were explained on the basis of the transition state theory and according to the Hughes and Ingold’s rule. Aqueous solutions alone produce metal powder having different size and irregular shape. The presence of polar organic solvents with high molecular weight and polarity produce powders having controlled size and regular morphology. The reason was because solvent polarity enhances the rate of red-ox reactions between metal ions and the reducing agent. The mean particle size of the powder was 60 um with zinc, 80 um with copper, and 90 um with lead. The extent of productivity was ≥98%. Results highlighted that the chemical reduction of the ionic species took place in a sequence steps. The first is a diffusion of the reactants across a boundary layer established at the polar site of the organic solvent molecules. The next step is the direct contact of the reactants. The third step involved reduction to yield powder. The last is the backward diffusion of the powder outside the boundary layer. Results showed that addition of water-miscible solvents having high dielectric constant increased the polarity of the medium. This energizes and enhances the one or more t step of the model to be more rapid to yield particles with small size and symmetrical shape.

Precipitation of calcium sulphate on hot walls - influence of impurities, thermal and hydraulic effects

International Nuclear Information System (INIS)

Guillermin, Roger

1973-01-01

After some generalities on desalination by distillation processes and on problems due to scaling, this research thesis aims at a better understanding of the formation of deposits and their effects in the case of precipitation of calcium sulphate hemihydrate which precipitates above 100 C in pure solution and between 100 and 300 C in brine. Deposit growth, influence of impurities, and influence of the deposit on heat exchange and loss of load are the main issues of this research. The author addresses general principles of salt crystallization and the thermodynamic and kinetic aspects of calcium sulphate precipitation, studies the growth kinetics of the calcium sulphate hemihydrate in a transient concentration regime, reports the study of thermal and hydraulic effects of the formation of a hemihydrate deposit, notably by discussing the different phases involved in the covering of a metallic surface

Biosorption characteristics of copper (II), chromium (III), nickel (II), and lead (II) from aqueous solutions by Chara sp. and Cladophora sp.

Science.gov (United States)

Elmaci, Ayşe; Yonar, Taner; Ozengin, Nihan

2007-09-01

The aim of this research was to expose individual removals of copper, chromium, nickel, and lead from aqueous solutions via biosorption using nonliving algae species, Chara sp. and Cladophora sp. Optimum pH values for biosorption of copper (II), chromium (III), nickel (II), and lead (II) from aqueous solutions were determined to be 6, 7, 7, and 3 for Cladophora sp. and 5, 3, 5, and 4 for Chara sp. respectively. Maximum adsorption capacities of Chara sp. [10.54 for chromium (III) and 61.72 for lead (II)] and Cladophora sp. [6.59 for chromium (III) and 16.75 and 23.25 for lead (II)] for chromium (III) and lead (II) are similar. On the other hand, copper (II) and nickel (II) biosorption capacity of Cladophora sp. [14.28 for copper (II) and 16.75 for nickel (II)] is greater than Chara sp. [6.506 for copper (II) and 11.76 for nickel (II)]. Significantly high correlation coefficients indicated for the Langmuir adsorption isotherm models can be used to describe the equilibrium behavior of copper, chromium, nickel, and lead adsorption onto Cladophora sp. and Chara sp.

Synthesis and characterization of copper nanofluid by a novel one-step method

International Nuclear Information System (INIS)

Kumar, S. Ananda; Meenakshi, K. Shree; Narashimhan, B.R.V.; Srikanth, S.; Arthanareeswaran, G.

2009-01-01

This paper presents a novel one-step method for the preparation of stable, non-agglomerated copper nanofluids by reducing copper sulphate pentahydrate with sodium hypophosphite as reducing agent in ethylene glycol as base fluid by means of conventional heating. This is an in situ, one-step method which gives high yield of product with less time consumption. The characterization of the nanofluid is done by particle size analyzer, X-ray diffraction topography, UV-vis analysis and Fourier transform infrared spectroscopy (FT-IR) followed by the study of thermal conductivity of nanofluid by the transient hot wire method

Electro-oxidation of methanol on copper in alkaline solution

International Nuclear Information System (INIS)

Heli, H.; Jafarian, M.; Mahjani, M.G.; Gobal, F.

2004-01-01

The electro-oxidation of methanol on copper in alkaline solutions has been studied by the methods of cyclic voltammetry, quasi-steady state polarization and chronoamperometry. It has been found that in the course of an anodic potential sweep the electro-oxidation of methanol follows the formation of Cu III and is catalysed by this species through a mediated electron transfer mechanism. The reaction also continues in the early stages of the reversed cycle until it is stopped by the prohibitively negative potentials. The process is diffusion controlled and the current-time responses follow Cottrellian behavior. The rate constants, turnover frequency, anodic transfer coefficient and the apparent activation energy of the electro-oxidation reaction are reported

Inhibition Effect of 1-Butyl-4-Methylpyridinium Tetrafluoroborate on the Corrosion of Copper in Phosphate Solutions

OpenAIRE

Scendo, M.; Uznanska, J.

2011-01-01

The influence of the concentration of 1-Butyl-4-methylpyridinium tetrafluoroborate (4MBPBF4) as ionic liquid (IL) on the corrosion of copper in 0.5 M P O 4 3 − solutions of pH 2 and 4 was studied. The research involved electrochemical polarization method, and scanning electron microscopy (SEM) technique. The results obtained showed that the inhibition efficiency of corrosion of copper increases with an increase in the concentration of 4MBPBF4 but decreases with increasing temperature. The the...

Removal of Sulphate and Manganese on Synthetic Wastewater in Sulphate Reducing Bioreactor Using Indonesian Natural Zeolite

Directory of Open Access Journals (Sweden)

Endah Retnaningrum

2017-07-01

Full Text Available The present research was conducted to investigate sulphate and manganese removal from synthetic wastewater. The continuous laboratory scale of down-flow fluidized-bed reactor (DFBR using sulphate reducing bacteria (SRB consortium and Indonesian natural zeolite as a bacterial support material was designed. At 9 days operation, maximum sulphate and manganese removal was observed to be 23% and 15.4%, respectively. The pH values were also changed to neutral. The population of SRB increased which effect on the raising of their activity for removing sulphate and manganese. Using the scanning electronic microscopy (SEM, it was observed that natural zeolite possesses excellent physical characteristics as a bacterial support material in DFBR. The imaging SEM result of SRB consortium on zeolite surface clearly showed the developed SRB biofilm on that particle. Analysis result of EDX confirmed that manganese was precipitated as manganese–sulfides.

Demonstration of immunogenic keratan sulphate in commercial chondroitin 6-sulphate from shark cartilage. Implications for ELISA assays

DEFF Research Database (Denmark)

Møller, H J; Møller-Pedersen, T; Damsgaard, T E

1995-01-01

The prototype monoclonal keratan sulphate (KS) antibody 5D4 that is widely used for detection of KS in tissues and biological fluids reacts strongly with commercial low grade shark cartilage chondroitin 6-sulphate. Characterization of the immunogenic material by chondroitinase ABC digestion, ELISA...... cartilage chondroitin 6-sulphate is an easy accessible source of immunogenic KS that can be used as a reference standard and as coating antigen in KS-ELISAs. The concentration of immunogenic KS in synovial fluid measured with an ELISA based solely on reagents of shark cartilage chondroitin 6-sulphate...... correlated well (r = 0.90) with the concentrations obtained with a traditional KS-ELISA that uses purified aggrecan as standard and coating antigen, and KS in both serum and synovial fluid could be measured with sufficient linearity....

Effectivness of dexametasone vs. Magnesium sulphate in postoperative analgesia: Dexametasone vs. Magnesium sulphate

Directory of Open Access Journals (Sweden)

Dautaj Brikena

2016-01-01

Full Text Available Introduction: Preoperative use of additive substances may be very helpful in perioperative acute pain management. Intravenous administration of dexametasone in preoperative period prevents postoperative nausea and vomiting but also provides better pain relief. It is also well known that magnesium sulphate (the NMDA receptor's antagonist by its central mechanism of action may be effective in postoperative pain control. Aim: The purpose of this study was to evaluate the effect of dexametasone and magnesium sulphate on postoperative pain management in patients undergoing abdominal surgery (open cholecystectomy. Methods: Seventy eight patients scheduled for elective surgery (open cholecystectomy were included in this study. This was the prospective cohort randomized placebo- controlled study. A total of 78 patients were randomized into three groups. Each group had twenty six patients. The group D, received dexametasone 0.1 mg/ kg iv 30 minutes before surgery. The group M received magnesium sulphate 3 mg/kg iv 30 minutes before surgery. The third group S was placebo group and patients in this group received saline in the same volume for each patient. For pain control after surgery all patients received tramadol 0.9-1.2 mg/kg and diklophenac 1.76 mg/kg. When necessary (VAS ≥ 7, morphine sulphate in dose 0.15 mg/kg was administred subcutaneously For treatment of emetic episodes metoclopramid 10 mg iv. was used. The patients were observed for intensity of pain measured VAS 0-10, pain relief and satisfaction with therapy, sedation, adverse events, emetic episodes and hemodynamic parameters. Results: There was no difference between groups regarding demographic data (age, gender, body weight, ASA score, comorbidity, duration of surgery and anesthesia and amount of fentanyl received during surgery. In group D 11.54% of patients received additional analgesia (morphine sulphate 0.15 mg/kg sc in the first 4 hours and 27% of patients in the first 24 hours

Influence of copper and formalin on the mycorrhiza of pine (Pinus kesiya Royle ex Gordon

Directory of Open Access Journals (Sweden)

G. D. Sharma

2014-08-01

Full Text Available Various concentrations of copper sulphate and formalin were tested for their effect on the efficiency of mycorrhizal functioning in pine seedlings. Low and higher doses of copper applied to the container grown seedling exhibited a less stimulatory effect than nedium doses. When applied in higher concentrations, the formalin caused mortality in young pine seedlings. The seedling yield and phosphate uptake was found maximum in 100 ppm applied concentration of copper. while słów growth and lower phosphate concentration was observed in the seedlings not given any copper treatment. Formalin at 50 ppm concentration slightly improved the seedling growth and phosphate uptake in mycorrhizal seedling as compared with untreated ones. Variation in the development and spread of ectomycorrhiza on the surface of roots of pine seedlings was also recorded in responses to copper and formalin treatments.

Biotreatment of Cr(VI) contaminated waters by sulphate reducing bacteria fed with ethanol

Energy Technology Data Exchange (ETDEWEB)

Pagnanelli, F., E-mail: francesca.pagnanelli@uniroma1.it [Department of Chemistry, Sapienza University of Rome, P.le Aldo Moro 5, 00185 Rome (Italy); Cruz Viggi, C., E-mail: carolina.cruzviggi@uniroma1.it [Department of Chemistry, Sapienza University of Rome, P.le Aldo Moro 5, 00185 Rome (Italy); Cibati, A., E-mail: alessio.cibati@uniroma1.it [Department of Chemistry, Sapienza University of Rome, P.le Aldo Moro 5, 00185 Rome (Italy); Uccelletti, D., E-mail: daniela.uccelletti@uniroma1.it [Department of Biology and Biotechnology, Sapienza University of Rome, P.le A. Moro 5, 00185 Rome (Italy); Toro, L., E-mail: luigi.toro@uniroma1.it [Department of Chemistry, Sapienza University of Rome, P.le Aldo Moro 5, 00185 Rome (Italy); Palleschi, C., E-mail: claudio.palleschi@uniroma1.it [Department of Biology and Biotechnology, Sapienza University of Rome, P.le A. Moro 5, 00185 Rome (Italy)

2012-01-15

Highlights: Black-Right-Pointing-Pointer Use of ethanol as electron donor for sulphate-reducing bacteria for the treatment of Cr(VI). Black-Right-Pointing-Pointer Isolation of contribution in Cr removal (adsorption vs. bioprecipitation). Black-Right-Pointing-Pointer Bioassessment of the process effectiveness by ecotoxicological in vivo tests using C. elegans. - Abstract: Biological treatment of Cr(VI) contaminated waters was performed in fixed bed reactors inoculated with SRB (sulphate-reducing bacteria) growing on ethanol. Treatment efficiency was evaluated by checking chemical abatement of Cr(VI) and by ecotoxicological tests using the nematode Caenorhabditis elegans. A preliminary comparison between ethanol and lactate was performed, denoting that using ethanol, the same values of final sulphate abatement were obtained. In addition ethanol showed to be a substrate more competitive than lactate in kinetic terms. Fixed bed column reactors were continuously fed with a solution containing sulphates (3 g L{sup -1}), ethanol (1.5 g L{sup -1}) and Cr(VI) (50 mg L{sup -1}). At steady state the column inoculated with SRB removed 65 {+-} 5% of sulphate and 95 {+-} 5% of chromium. Bioactive removal mechanisms predominated over biosorption. Diminution of Cr(VI) toxicity was assessed by using the nematode C. elegans as a test organism showing that the survival of nematodes was 20% in the presence of the untreated influent and raised up to 53% when the nematodes were exposed to the treated effluent.

Copper vertical micro dendrite fin arrays and their superior boiling heat transfer capability

Science.gov (United States)

Wang, Ya-Qiao; Lyu, Shu-Shen; Luo, Jia-Li; Luo, Zhi-Yong; Fu, Yuan-Xiang; Heng, Yi; Zhang, Jian-Hui; Mo, Dong-Chuan

2017-11-01

Micro pin fin arrays have been widely used in electronic cooling, micro reactors, catalyst support, and wettability modification and so on, and a facile way to produce better micro pin fin arrays is demanded. Herein, a simple electrochemical method has been developed to fabricate copper vertical micro dendrite fin arrays (Cu-VMDFA) with controllable shapes, number density and height. High copper sulphate concentration is one key point to make the dendrite stand vertically. Besides, the applied current should rise at an appropriate rate to ensure the copper dendrite can grow vertically on its own. The Cu-VMDFA can significantly enhance the heat transfer coefficient by approximately twice compared to the plain copper surface. The Cu-VMDFA may be widely used in boiling heat transfer areas such as nuclear power plants, electronic cooling, heat exchangers, and so on.

Leach-SX-EW copper revalorization from overburden of abandoned copper mine Cerovo, Eastern Serbia

Directory of Open Access Journals (Sweden)

Stevanović Z.

2009-01-01

Full Text Available Hydrometallurgical processes for copper revalorization from overburden of abandoned mine Cerovo in Eastern Serbia were studied. Paper contain results of percolation leaching tests, performed with acidic mine waters accumulated in the bottom of the former open pit, followed by solvent extraction (SX and electrowinning (EW processes on achieved copper pregnant leach solutions. Usage of accumulated waste waters was objected to minimizing the environmental hazard due to uncontrolled leaking of these waters in nearby creeks and rivers. Chemical composition of acidic mine waters used for leaching tests was: (g/dm3: Cu - 0.201; Fe - 0.095; Mn - 0.041; Zn - 0.026; Ni - 0.0004; pH value - 3.3. Copper content in overburden sample used for leaching tests was 0.21% from which 64% were oxide copper minerals. In scope of leaching tests were examined influence of leaching solution pH values and iron (III concentration on copper recovery. It was established that for 120 hours of leaching on pH=1.5 without oxidant agents, copper concentration in pregnant leach solutions enriched up to 1.08g/dm3 which was enough for copper extraction from solution with SX-EW treatment. As extraction reagent in SX circuit was used LIX-984N in a kerosene diluent. Cathode current density in electrowinning cell was 220Am-2 while electrolyte temperature was kept on 50±2oC. Produced cathode copper at the end of SX-EW process has purity of 99.95% Cu.

Electrodeposited porous and amorphous copper oxide film for application in supercapacitor

Energy Technology Data Exchange (ETDEWEB)

Patake, V.D. [Thin Film Physics Laboratory, Department of Physics, Shivaji University, Kolhapur 416004, (M.S.) (India); Joshi, S.S. [Clean Energy Research Center, Korea Institute of Science and Technology, Cheongryang, Seoul 130-650 (Korea, Republic of); Lokhande, C.D. [Thin Film Physics Laboratory, Department of Physics, Shivaji University, Kolhapur 416004, (M.S.) (India); Clean Energy Research Center, Korea Institute of Science and Technology, Cheongryang, Seoul 130-650 (Korea, Republic of)], E-mail: l_chandrakant@yahoo.com; Joo, Oh-Shim [Clean Energy Research Center, Korea Institute of Science and Technology, Cheongryang, Seoul 130-650 (Korea, Republic of)], E-mail: joocat@kist.rre.kr

2009-03-15

In present study, the porous amorphous copper oxide thin films have been deposited from alkaline sulphate bath. The cathodic electrodeposition method was employed to deposit copper oxide film at room temperature on stainless steel substrate. Their structural and surface morphological properties were investigated by means of X-ray diffraction (XRD) and scanning electron micrograph (SEM), respectively. To propose this as a new material for possible application in the supercapacitor, its electrochemical properties have been studied in aqueous 1 M Na{sub 2}SO{sub 4} electrolyte using cyclic voltammetry. The structural analysis from XRD pattern showed the formation of amorphous copper oxide film on the substrate. The surface morphological studies from scanning electron micrographs revealed the formation of porous cauliflower-like copper oxide film. The cyclic voltammetric curves showed symmetric nature and increase in capacitance with increase in film thickness. The maximum specific capacitance of 36 F g{sup -1} was exhibited for the 0.6959 mg cm{sup -2} film thickness. This shows that low-cost copper oxide electrode will be a potential application in supercapacitor.

The solvent extraction of cerium from sulphate solution - mini plant trials

International Nuclear Information System (INIS)

Soldenhoff, K.; Wilkins, D.; Ring, R.

1998-01-01

Full text: The Mt. Weld deposit in Western Australia has a complex rare earth mineralisation. The rare earth phosphate minerals, which include monazite, are amenable to conventional caustic cracking followed by hydrochloric acid dissolution of the trivalent rare earths. The presence of the mineral cerianite in the ore, which is unaffected by the alkali attack, results in rejection of a considerable proportion of the cerium to the acid leach residue. The recovery of cerium from a sulphate solution, resulting from the processing of such a residue, is the subject of the current paper. The liquor treated by solvent extraction contained 63 g L -1 rare earths and the cerium to total rare earth ratio was 75%. Other impurities, including Fe and Th, totalled 2000 ppm. A solvent mixture of commercially available extractants in a low aromatic content diluent was used to extract Ce 4+ selectively over the trivalent rare earths. Partial co-extraction of Fe and Th occurred but it was found that these elements were not easily stripped and therefore selective back extraction of cerium was possible. The cerium was stripped from the organic phase by hydrochloric acid and hydrogen peroxide. In continuous counter-current trials two extraction stages and three strip stages were used. In order to produce two grades of strip liquor, stripping was divided into two circuits. The first strip circuit consisting of a single stage, contained proportionally more of the trivalent rare earths. The second strip circuit, consisting of two stages, removed the remaining cerium with proportionally less of the rare earths. A bleed solvent stream was treated for removal of impurities to prevent build-up in the solvent. In the continuous counter current trials, 95% Ce 4+ extraction was achieved and the Ce to total rare earth ratio was upgraded to > 99%

Demonstration of immunogenic keratan sulphate in commercial chondroitin 6-sulphate from shark cartilage. Implications for ELISA assays

DEFF Research Database (Denmark)

Møller, H J; Møller-Pedersen, T; Damsgaard, T E

1995-01-01

The prototype monoclonal keratan sulphate (KS) antibody 5D4 that is widely used for detection of KS in tissues and biological fluids reacts strongly with commercial low grade shark cartilage chondroitin 6-sulphate. Characterization of the immunogenic material by chondroitinase ABC digestion, ELISA...... inhibition studies, immunoblotting and HPLC analyses confirmed the presence of substantial amounts of KS, probably as a large proteoglycan (> 120 kDa). Commercial and heterogenic glycosaminoglycan preparations therefore must be used with great caution in immunological analyses. On the other hand the shark...... cartilage chondroitin 6-sulphate is an easy accessible source of immunogenic KS that can be used as a reference standard and as coating antigen in KS-ELISAs. The concentration of immunogenic KS in synovial fluid measured with an ELISA based solely on reagents of shark cartilage chondroitin 6-sulphate...

Superhydrophobic copper surfaces fabricated by fatty acid soaps in aqueous solution for excellent corrosion resistance

Energy Technology Data Exchange (ETDEWEB)

Xu, Wenlong; Hu, Yuanyuan; Bao, Wenda; Xie, Xiaoyu; Liu, Yiran; Song, Aixin, E-mail: songaixin@sdu.edu.cn; Hao, Jingcheng

2017-03-31

Highlights: • The superhydrophobic property can be realized in a much quicker process (7.5 min) in aqueous solution than in ethanol. • The fabrication process of superhydrophobic metal surfaces greatly increases the safety in industrial manufacture in commercial scale. • The superhydrophobic copper surfaces show excellent corrosion resistance. - Abstract: A simple and safe one-step immersion method was developed to obtain the stable superhydrophobic copper surfaces with excellent corrosion resistance ability using fatty acids in water-medium instead of ethanol. An organic alkali, N,N-dimethylcyclohexylamine (DMCHA), was chosen to solve the poor solubility of fatty acids in water and the high Krafft point of carboxylate salts with inorganic counterions. The superhydrophobic property can be realized in a much quicker process (7.5 min) in aqueous solution than in ethanol (more than 2 d), which is universally feasible for the fabrication of superhydrophobic metal surfaces in industry scale, thereby greatly increasing the safety in industrial manufacture.

Sulphate deposition by precipitation into Lake Ontario

Energy Technology Data Exchange (ETDEWEB)

Shaw, R W; Whelpdale, D M

1973-01-01

Measurements of sulphate concentration in precipitation from individual snow storms of several hours duration in the western Lake Ontario region indicate that approximately 9-66 mg/M/sub 2/ of SO/sub 4//sup 2 -/ is being deposited into the lake per storm. This amount is up to several times more than daily average values over long periods found by other workers. Using a mean sulphate concentration of 4 mg/l and an annual accumulation of precipitation of 760 mm, the yearly sulphate deposition by precipitation is about 0.1% of the total mass of sulphate in the lake; however, more significantly, it is of the same order of magnitude as that discharged directly into the lake by industry.

Recovery of uranium from copper leaching solutions from the South Chuquicamata mine

International Nuclear Information System (INIS)

Andalaft, N.; Soto, R.

1980-01-01

The paper deals with the recovery of uranium from copper leaching solutions containing between 10 and 18 ppm U 3 O 8 . The study, which covers a laboratory stage and a pilot plant stage, has shown the technical feasibility of producing yellow cake with U 3 O 8 contents of between 13 and 20% by direct precipitation of eluates which, when purified in the laboratory, have contained up to some 85% U 3 O 8 . (author)

Mortar and concrete based on calcium sulphate binders

NARCIS (Netherlands)

Bakker, J.J.F.; Brouwers, H.J.H.; Fischer, H.B

2006-01-01

In this study both hemi-hydrate and anhydrite are tested as calcium sulphate binders for structural mortar and concrete. The advantage of using calcium sulphates instead of cement as a binder is the fact that the production of calcium sulphate is more environmental friendly than that of cement. For

Topical therapy of acne vulgaris using 2% tea lotion in comparison with5% Zinc sulphate lotion

International Nuclear Information System (INIS)

Sharquie, Khalifa E.; Noaimi, Adil A.; Al-Salih, Mazin M.

2008-01-01

Objective was to evaluate effectiveness of 2% tea lotion in comparisonwith 5% zinc sulphate solution in the treatment of acne vulgaris. This is asingle-blind randomly comparative therapeutic clinical trial carried out inthe Department of Dermatology, Baghdad Teaching Hospital, Iraq from June 2006to December 2007. Full history and clinical examination were studied for eachpatient regarding all relevant points of the disease, to evaluate theseverity of acne. Forty-seven patients with acne vulgaris were dividedrandomly into 2 groups and were instructed to use the following solutionstwice daily for 2 months; group A used 2% tea lotion, group B used 5% zincsulphate lotion. Patients with papulopustular lesions were included in thestudy, while patients with severe acne were excluded. The clinicalimprovement was scored by counting the number of inflammatory lesions beforeand after treatment. Forty patients completed the study, their ages rangedfrom 13-27 years with a mean+-standard deviation of 19.5+-3.5 years with 20patients in each group. Two percent tea lotion was statistically significantin decreasing the number of the inflammatory lesions in acne vulgaris, while5% zinc sulphate solution was beneficial, but did not reach statisticallysignificant level as tea lotion. Two percent of tea lotion was a goodalternative remedy to be used in the treatment of acne vulgaris and was muchsuperior than topical 5% zinc sulphate solution. (author)

Spectrophotometric determination of copper in alkaline solutions and evaluation of some hydroxy-substituted 1,10-phenanthrolines as chromogenic reagents.

Science.gov (United States)

Dunbar, W E; Schilt, A A

1972-09-01

Seven new hydroxy-substituted 1,10-phenanthroline derivatives have been evaluated as chromogenic reagents for the determination of copper in strongly alkaline solution. The most sensitive of these, 2,9-dimethyl-4,7-dihydroxy-1,10-phenanthroline, has proven to be highly effective in a simple, rapid procedure for determining trace amounts of copper in sodium hydroxide, potassium carbonate, sodium phosphate or ammonium hydroxide.

Sulphate reduction and vertical distribution of sulphate-reducing bacteria quantified by rRNA slot-blot hybridization in a coastal marine sediment

DEFF Research Database (Denmark)

Sahm, K.; MacGregor, BJ; Jørgensen, BB

1999-01-01

In the past, enumeration of sulphate-reducing bacteria (SRB) by cultivation-based methods generally contradicted measurements of sulphate reduction, suggesting unrealistically high respiration rates per cell. Here, we report evidence that quantification of SRB rRNA by slot-blot hybridization......, directly above the sulphate reduction maximum. Cell numbers calculated by converting the relative contribution of SRB rRNA to the percentage of DAPI-stained cells indicated a population size for SRB of 2.4-6.1 x 10(8) cells cm(-3) wet sediment. Cellular sulphate reduction rates calculated on the basis...

Thermodynamic evaluation of Cu-H-O-S-P system - Phase stabilities and solubilities for OFP-copper

International Nuclear Information System (INIS)

Magnusson, Hans; Frisk, Karin

2013-04-01

A thermodynamic evaluation for Cu-H-O-S-P has been made, with special focus on the phase stabilities and solubilities for OFP-copper. All binary systems including copper have been reviewed. Gaseous species and stoichiometric crystalline phases have been included for higher systems. Sulphur in OFP-copper will be found in sulphides. The sulphide can take different morphologies but constant stoichiometry Cu 2 S. The solubility of sulphur in FCC-copper reaches ppm levels already at 550 deg C and decreases with lower temperature. No phosphorus-sulphide will be stable, although the copper sulphide can be replaced by copper sulphates at high partial pressure oxygen like in the oxide scale. Phosphorus has a high affinity to oxygen, and phosphorus oxide P 4 O 10 and copper phosphates (Cu 2 P 2 O 7 and Cu 3 (PO 4 ) 2 ) are all more stable than copper oxide Cu 2 O. With hydrogen present at atmospheric pressure, copper phosphates Cu 2 P 2 O 7 and Cu 3 (P 2 O 6 OH) 2 are both more stable than water vapour or aqueous water at temperatures below 400 deg C. At high pressure conditions, the copper phosphates can be reduced giving water. However, the phosphates are still more stable than water vapour. The solubility limit of phosphorus in FCC-copper at 25 deg C is 510 ppm, in equilibrium with copper phosphide Cu 3 P. The major part of phosphorus in OFP-copper will be in solid solution. Oxygen in FCC-copper has a very low solubility. In the presence of a strong oxide forming element such as phosphorus in OFP-copper, the solubility decreases even more. Copper oxides will become stable first when all phosphorus has been consumed, which takes place at twice the phosphorus content, calculated in weight. Hydrogen has a low solubility in copper, calculated as 0.1 ppm at 675 deg C. No crystalline hydrogen phase has been found stable at atmospheric pressures and above 400 deg C. At lower temperatures the hydrogen containing phosphate Cu 3 (P 2 O 6 OH) 2 can become stable. Measured hydrogen

The effect of the cooling rate during quenching, electron bombardment and plastic deformation on the kinetics of a solid solution disintegration in iron-copper alloys

International Nuclear Information System (INIS)

Fedorov, G.B.; Zhukov, V.P.; Braun, A.G.; Smirnov, E.A.

1974-01-01

From the electroresistivity variation at 77 0 K, the influence of nonequilibrium point defect density and of complexes and dislocations on the decay process of the iron-copper solid solution is determined. Owing to high quenching rate of thin foils, isochrones of their electroconductivity curves appear shifted by about 200 0 C to lower temperatures. For quenched and irradiated specimens at 200-250 0 C a sharp retardation of electroconductivity decline is observed due to a zone stage. The plastic deformation (15%) leads to a partial suppression of that stage. Both irradiation and deformation initiate the process of copper separation from the solid solution, the latter being the stronger, the more copper is in the solid solution

Pitting corrosion of copper. An equilibrium - mass transport study

International Nuclear Information System (INIS)

Taxen, C.

2002-08-01

A mathematical model for the propagation of corrosion pits is described and used to calculate the potentials below which copper is immune to pitting. The model uses equilibrium data and diffusion coefficients and calculates the stationary concentration profiles of 26 aqueous species from the bulk water outside a corrosion pit to the site of the metal dissolution. Precipitation of oxides and salts of copper is considered. Studied conditions include water compositions from tap waters to seawater at the temperatures 25 deg C and 75 deg C. Carbonate and sulphate are aggressive towards copper because of complex formation with divalent copper. Carbonate is less aggressive in a corrosion pit than outside at the pH of the bulk. Carbonate carries acidity out from the pit, favours oxide formation and may prevent the initiation of acidic corrosion pits. The concentration profiles are used to estimate the maximum propagation rates for a corrosion pit. A high potential is found to be the most important factor for the rate of propagation. The levels of potential copper can sustain, as corrosion potentials are discussed in terms of the stability of cuprous oxide as a cathode material for oxygen reduction relative to non-conducting cupric phases

Pitting corrosion of copper. An equilibrium - mass transport study

Energy Technology Data Exchange (ETDEWEB)

Taxen, C. [Swedish Corrosion Inst., Stockholm (Sweden)

2002-08-01

A mathematical model for the propagation of corrosion pits is described and used to calculate the potentials below which copper is immune to pitting. The model uses equilibrium data and diffusion coefficients and calculates the stationary concentration profiles of 26 aqueous species from the bulk water outside a corrosion pit to the site of the metal dissolution. Precipitation of oxides and salts of copper is considered. Studied conditions include water compositions from tap waters to seawater at the temperatures 25 deg C and 75 deg C. Carbonate and sulphate are aggressive towards copper because of complex formation with divalent copper. Carbonate is less aggressive in a corrosion pit than outside at the pH of the bulk. Carbonate carries acidity out from the pit, favours oxide formation and may prevent the initiation of acidic corrosion pits. The concentration profiles are used to estimate the maximum propagation rates for a corrosion pit. A high potential is found to be the most important factor for the rate of propagation. The levels of potential copper can sustain, as corrosion potentials are discussed in terms of the stability of cuprous oxide as a cathode material for oxygen reduction relative to non-conducting cupric phases.

Biomass reduction of Salvinia molesta exposed to copper sulfate pentahydrate (CuSO4.5H2O)

OpenAIRE

Barros,João Pedro Alves de Azevedo; Henares,Matheus Nicolino Peixoto

2015-01-01

Copper in the aquatic ecosystem may remain adsorbed or be incorporated into the biomass and undergo biomagnification causing unwanted effects to aquatic macrophyte communities. This study evaluated the biomass reduction of Salvinia molesta (Mitchell) exposed to copper sulphate pentahydrate (CuSO4.5H2O) under laboratory conditions. Approximately 20.5 g of fresh mass (FM) of S. molesta (0.74 g dry matter, DM) were placed in glass tanks with different concentrations (n = 3) of CuSO4.5H2O as foll...

Sulphate reduction and vertical distribution of sulphate-reducing bacteria quantified by rRNA slot-blot hybridization in a coastal marine sediment

DEFF Research Database (Denmark)

Sahm, K.; MacGregor, BJ; Jørgensen, BB

1999-01-01

In the past, enumeration of sulphate-reducing bacteria (SRB) by cultivation-based methods generally contradicted measurements of sulphate reduction, suggesting unrealistically high respiration rates per cell. Here, we report evidence that quantification of SRB rRNA by slot-blot hybridization...... between 18% and 25% to the prokaryotic rRNA pool. The dominant SRB were related to complete oxidizing genera (Desulphococcus, Desulphosarcina and Desulphobacterium), while Desulpho-bacter could not be detected. The vertical profile and quantity of rRNA from SRB was compared with sulphate reduction rates......, directly above the sulphate reduction maximum. Cell numbers calculated by converting the relative contribution of SRB rRNA to the percentage of DAPI-stained cells indicated a population size for SRB of 2.4-6.1 x 10(8) cells cm(-3) wet sediment. Cellular sulphate reduction rates calculated on the basis...

EPR studies on binuclear copper(II) complexes with N,N',N'',N'''-tetrakis(2-pyridylmethyl)-1,4,8,11-tetraaza-cyclotetradecane in solutions

International Nuclear Information System (INIS)

Jezierska, J.; Ozarowski, A.; Vuckovic, G.

1997-01-01

Binuclear copper(II) complexes of macrocyclic ligand TMPC (tetraazamacrocycle with four pendant 2-pirydylmethyl groups attached to the ring nitrogen atoms) with various anions forming bridge between copper ions, or coordinating to copper(II) ions at the apex, were prepared and their frozen solutions in DMF and NMF were investigated by EPR. The spectroscopic results have been interpreted in terms of molecular structure of investigated complexes

Copper Leaching from Copper-ethanolamine Treated Wood: Comparison of Field Test Studies and Laboratory Standard Procedures

OpenAIRE

Nejc Thaler; Miha Humar

2014-01-01

Copper-based compounds are some of the most important biocides for the protection of wood in heavy duty applications. In the past, copper was combined with chromium compounds to reduce copper leaching, but a recent generation of copper-based preservatives uses ethanolamine as a fixative. To elucidate the leaching of copper biocides from wood, Norway spruce (Picea abies) wood was treated with a commercial copper-ethanolamine solution with two different copper concentrations (cCu = 0.125% and 0...

Sulphate rocks as an arena for karst development

Directory of Open Access Journals (Sweden)

Andrejchuk V.

1996-01-01

Full Text Available The rocks in which karst systems develop are most commonly composed of carbonate sulphate and chloride minerals. The sulphate minerals are quite numerous, but only gypsum and anhydrite form extensive masses in sedimentary sequences. Other minerals, which represent sulphates of K, Mg and Na, normally occur as minor beds (0.1-5.0 m, or as inclusions associated with chloride rocks. However some minerals precipitated in salt-generating basins, such as mirabilite and glauberite (typically formed in the Kara-Bogaz-Gol Gulf, salt lakes of Siberia and in China, form sequences up to 5-10 m thick where karst may develop. Due to the very high solubility of Na -sulphates, karst processes and features occurring in these rocks resemble salt karst. Thus, the term sulphate karst, although not strictly correct, is used mainly to indicate karst developed in gypsum and anhydrite.

Occurrence of sulphate reducing bacteria (SRB) associated with biocorrosion on metallic surfaces in a hydroelectric power station in Ibirama (SC) - Brazil

OpenAIRE

Paulo Roberto Dantas Marangoni; Diogo Robl; Marcos Antonio Coelho Berton; Carlos Mario Garcia; Angela Bozza; Mariana Vieira Porsani; Patricia do Rocio Dalzoto; Vânia Aparecida Vicente; Ida Chapaval Pimentel

2013-01-01

The aim of this study was evaluate, two methods for the detection and identification of sulphate reducing bacteria (SRB): ML medium and PCR with specific primers for SRB groups. SRB were detected through the selective medium only on carbon steel, which showed corrosion. Employing specific PCR primer, SBR were detected from all the metallic components assayed, even those that did not present visible corrosion spots, such stainless steel and copper alloys. Despite the presence or absence of cor...

Abiotic nitrate and sulphate reduction by hydrogen: a comparative experimental study

International Nuclear Information System (INIS)

Truche, L.; Berger, G.; Albrecht, A.; Giffaut, E.

2010-01-01

Document available in extended abstract form only. The bituminous waste which is part of the intermediate level, long-lived waste (MAVL) is characterised, amongst others, by the coexistence of nitrates, sulphates, organic matter, native metals and hydrogen gas in the waste mixture and package. It can be considered as the most complex example that will be used to discuss redox reactions occurring in such waste mixtures. The evaluation of the redox conditions requires quantification of the amount of electron acceptors and donors and definition of the kinetics of redox reaction. The objectives of an experimental study to unravel some of these reaction complexities are: - to investigate nature and rate of sulphate and nitrate reduction by hydrogen in the presence of different catalysts (stainless steel, hastelloy, magnetite and argillite); - to compare sulphate and nitrate as electron acceptors; - to provide a mechanistic model of these reactions. It is well known that reduction of sulphate and nitrate requires high activation energies, usually supplied either by thermal processes or via bacterial and surface catalysis, of which the latter has been investigated in this study. Preliminary experiments performed at 150 deg. C and under H 2 pressure show that sulphate reduction is enhanced in the presence of magnetite, but essentially under the restricted condition of low sulphate concentration and at a pH below the Point of Zero Charge of magnetite. This suggests that sorption of sulphate contributes to the catalysed reaction (at low pH) but provided that the magnetite surface sites are not saturated with respect to aqueous sulphate (low concentration). On the contrary, nitrate reduction is observed whatever the pH and the nitrate concentration in the presence of both magnetite and hastelloy C276 (Ni, Cr, Mo, W, Fe alloy). The effect of temperature on the rate of nitrate reduction (500 ppm KNO 3 solution) is shown by comparing three different experiments conducted in

[Photometric determination of butyl "aeroflot" flotation agent (sodium dibutyl dithiophosphate) in the air of work zone and skin washings].

Science.gov (United States)

Dorogova, V B; Kucheriavykh, E I; Sokolova, T V

1989-01-01

Photometric procedure of butyl "aeroflot" identification in the work zone air and in wash-out from workers' integument was developed, The procedure was based on the formation of yellow- and orange-dyed copper dibutyl dithiophosphate under butyl "aeroflot" interaction with copper sulphate with the subsequent photometry of dyed solutions for the wavelength of 420 nm in the 10-mm cell. Buffer solution with pH-9.2 was used as an absorbing solution for the workplace air sampling and integument wash-out.

Process of converting actinide ions present in the solid residues of a sulphating process for radioactive solid waste containing actinides into a useful state

International Nuclear Information System (INIS)

Wieczorek, H.; Oser, B.

1985-01-01

Stages of the process: a) The residue is dissolved in water or 1 to 2 mole nitric acid, where the greater part is dissolved. b) The solution formed is separated from the insoluble part of the residue and is heated to a temperature below its boiling point. c) The hot solution has an aquaeous barium nitrate solution added to it with a quantity which slightly exceeds that required for the stochiometric complete precipitation of the sulphate ions. The solution is kept at the selected temperature for a period of 0.5 to 2 hours. d) After subsequent cooling to room temperature, the precipitated barium sulphate is separated and e) the actinide-nitrate solution is fed into an extractive reprocessing process. (orig./PW) [de

Intramolecular synergistic effect of glutamic acid, cysteine and glycine against copper corrosion in hydrochloric acid solution

International Nuclear Information System (INIS)

Zhang Daquan; Xie Bin; Gao Lixin; Cai Qirui; Joo, Hyung Goun; Lee, Kang Yong

2011-01-01

The corrosion protection of copper by glutamic acid, cysteine, glycine and their derivative (glutathione) in 0.5 M hydrochloric acid solution has been studied by the electrochemical impedance spectroscopy and cyclic voltammetry. The inhibition efficiency of the organic inhibitors on copper corrosion increases in the order: glutathione > cysteine > cysteine + glutamic acid + glycine > glutamic acid > glycine. Maximum inhibition efficiency for cysteine reaches about 92.9% at 15 mM concentration level. The glutathione can give 96.4% inhibition efficiency at a concentration of 10 mM. The molecular structure parameters were obtained by PM3 (Parametric Method 3) semi-empirical calculation. The intramolecular synergistic effect of glutamic acid, cysteine and glycine moieties in glutathione is attributed to the lower energy of the lowest unoccupied molecular orbital (E LUMO ) level and to the excess hetero-atom adsorption centers and the bigger coverage on the copper surface.

Effect of Ammonium Chloride on the Efficiency with Which Copper Sulfate Activates Marmatite: Change in Solution Composition and Regulation of Surface Composition

Directory of Open Access Journals (Sweden)

Shengdong Zhang

2018-06-01

Full Text Available Zinc sulfide minerals are the primary choice for zinc extraction and marmatite is one of the two most common zinc sulphide minerals (sphalerite and marmatite, therefore it is of great significance to study and optimize the flotation of marmatite. To improve the activation of copper sulfate on marmatite, a method involving the addition of ammonium chloride is devised. The method has been proven to be an effective way of improving the activation efficiency of copper sulfate towards marmatite under alkaline conditions. The strengthening mechanism was studied using micro-flotation, adsorption test, X-ray photoelectron spectroscopy, and by analyzing changes in solution composition. Flotation test results show that the activation effect of the copper sulfate towards marmatite is enhanced with the addition of ammonium chloride. According to the results of the adsorption measurements and X-ray photoelectron spectroscopy analysis, when the marmatite surface is activated using copper sulfate with added ammonia chloride, it adsorbs more copper sulfide and less copper hydroxide and zinc hydroxide. These changes in surface composition are believed to occur via the following process: NH3(aq promotes the dissolution of zinc hydroxide and then facilitates the conversion of surface copper hydroxide to copper sulfide. In addition, the occurrence of Cu(NH3n2+ can promote the adsorption of copper ions (Cu2+ can be stored as Cu(NH3n2+ via complexation, and then, when the concentration of copper ions decreases, Cu2+ can be released through the decompositionof Cu(NH3n2+. Hence, the copper ion concentration can be maintained and this can facilitate the adsorption of Cu2+ on marmatite. Based on a comprehensive analysis of all our results, we propose that adding ammonium chloride to the copper sulfate changes the solution components (i.e., the presence of NH3(aq and Cu(NH3n2+ and then regulates the surface composition of marmatite. The change in surface composition

Sulphate reduction experiment: SURE-1

International Nuclear Information System (INIS)

Pedersen, K.; Arlinger, J.; Bengtsson, A.; Edlund, J.; Eriksson, L.; Hallbeck, L.; Johansson, J.; Paeaejaervi, A.; Rabe, L.

2013-11-01

It was previously concluded that opposing gradients of sulphate and methane, observations of 16S rDNA sequences displaying great similarity to those of anaerobic methane-oxidizing Archaea, and a peak in sulphide concentration in groundwater from a depth of 250-350 m in Olkiluoto, Finland, indicated proper conditions for methane oxidation with sulphate. In the present research (SURE-1), pressure-resistant, gas-tight circulating systems were constructed to enable the investigation of attached and unattached anaerobic microbial populations from a depth of 327 m in Olkiluoto under in situ pressure (2.4 MPa), diversity, dissolved gas, and hydrochemical conditions of groundwater station ONKPVA6. Three parallel flow cell cabinets were configured to allow observation of the influence on microbial metabolic activity of 11 mM methane, 11 mM methane plus 10 mM H 2 , or 2.1 mM O 2 plus 7.9 mM N 2 (i.e., air). The concentrations of these gases and of organic acids and carbon, sulphur chemistry, pH and E h , ATP, numbers of cultivable microorganisms, and total numbers of cells and bacteriophages were subsequently recorded under batch conditions for 105 d. The system containing H 2 and methane displayed microbial reduction of 0.7 mM sulphate to sulphide, while the system containing only methane produced 0.2 mM reduced sulphate. The system containing added air became inhibited and displayed no signs of microbial activity. Added H 2 and methane induced increasing numbers of lysogenic bacteriophages per cell. It appears possible that a microbial anaerobic methane-oxidizing process coupled to acetate formation and sulphate reduction may be ongoing in aquifers at a depth of 250-350 m in Olkiluoto, but clear evidence of such an AOM process was not obtained. (orig.)

Sulphate reduction experiment: SURE-1

Energy Technology Data Exchange (ETDEWEB)

Pedersen, K.; Arlinger, J.; Bengtsson, A.; Edlund, J.; Eriksson, L.; Hallbeck, L.; Johansson, J.; Paeaejaervi, A.; Rabe, L. [Microbial Analytics Sweden AB, Moelnlycke (Sweden)

2013-11-15

It was previously concluded that opposing gradients of sulphate and methane, observations of 16S rDNA sequences displaying great similarity to those of anaerobic methane-oxidizing Archaea, and a peak in sulphide concentration in groundwater from a depth of 250-350 m in Olkiluoto, Finland, indicated proper conditions for methane oxidation with sulphate. In the present research (SURE-1), pressure-resistant, gas-tight circulating systems were constructed to enable the investigation of attached and unattached anaerobic microbial populations from a depth of 327 m in Olkiluoto under in situ pressure (2.4 MPa), diversity, dissolved gas, and hydrochemical conditions of groundwater station ONKPVA6. Three parallel flow cell cabinets were configured to allow observation of the influence on microbial metabolic activity of 11 mM methane, 11 mM methane plus 10 mM H{sub 2}, or 2.1 mM O{sub 2} plus 7.9 mM N{sub 2} (i.e., air). The concentrations of these gases and of organic acids and carbon, sulphur chemistry, pH and E{sub h}, ATP, numbers of cultivable microorganisms, and total numbers of cells and bacteriophages were subsequently recorded under batch conditions for 105 d. The system containing H{sub 2} and methane displayed microbial reduction of 0.7 mM sulphate to sulphide, while the system containing only methane produced 0.2 mM reduced sulphate. The system containing added air became inhibited and displayed no signs of microbial activity. Added H{sub 2} and methane induced increasing numbers of lysogenic bacteriophages per cell. It appears possible that a microbial anaerobic methane-oxidizing process coupled to acetate formation and sulphate reduction may be ongoing in aquifers at a depth of 250-350 m in Olkiluoto, but clear evidence of such an AOM process was not obtained. (orig.)

Removal of Copper (II Ions in Aqueous Solutions by Sorption onto Alkali Activated Fly Ash

Directory of Open Access Journals (Sweden)

Darmayanti Lita

2018-01-01

Full Text Available Fly ash is a particulate material produced from coal combustion power plants with major components are silica, alumina, iron oxide, calcium oxide, magnesium oxide, and carbon which are ideal for metal adsorbents. The potential use of fly ash in the wastewater treatment process is obvious because it can be obtained cheaply in large quatities and it can be used as an adsorbent. However, fly ash still shows lower adsorption capacity unless it is activated. In this study, fly ash activated by NaOH 14 M and KOH 14 M solutions. The batch experiments were carried out to study the sorption of copper ions from aqueous on alkali activated fly ash. The influence of initial concentration and contact time were examined at constant pH and dose of adsorbent. The sorption capacity of copper ions increased with the initial concentration and contact time. The sorption capacities followed the order Na1>Ka1>FA. The adsorption isotherm model exhibited that the Langmuir model is very suitable with copper ions adsorption onto fly ash and alkali activated fly ash. Kinetic study shows that adsorption of copper ions onto FA, Na1, and Ka1 follows the pseudo second-order kinetics.

Copper naphthenate: a proven solution for new wood preservative problems

Energy Technology Data Exchange (ETDEWEB)

McNair, W.S. [Merichem Chemicals and Refinery Services LLC, Houston, TX (United States); Loecner, P. [Pacific Gas and Electric, Davis, CA (United States)

2002-08-01

Today's engineers have the responsibility of considering cost, availability and climbability, as well as the environmental alternatives available to the traditional wood preservatives used in the production of utility poles: creosote, pentachlorophenol (PCP) and chromated copper arsenate (CCA). The leading alternative now emerging for utilities in this field is copper naphthenate. The authors present a case study that clearly demonstrates copper naphthenate as one of the most environmentally sensitive and effective wood preservative. When first introduced, copper naphthenate seemed to frequently result in early failure of the poles treated with this preservative. It was discovered that it was a phenomenon that had been largely exaggerated, and the failure rate was less than one per cent. A recent review has concluded that premature failures have basically disappeared. Several reasons can explain premature failures, such as pretreatment decay, improper sterilization/conditioning/drying, inadequate copper penetration and retention, and others. The long term effectiveness and performance of copper naphthenate has been documented in a number of field trials. The ultimate disposal of the product must be considered by the specifying engineer, and it is possible to dispose of copper naphthenate poles in a sanitary landfill. Due in part to recent manufacturing economies, the cost of copper naphthenate is similar to other oil-borne treatments. The case study of Pacific Gas and Electric was discussed. 7 refs., 2 figs.

Sulphate Removal from Water by Carbon Residue from Biomass Gasification: Effect of Chemical Modification Methods on Sulphate Removal Efficiency

Directory of Open Access Journals (Sweden)

Hanna Runtti

2016-02-01

Full Text Available Sulphate removal from mine water is a problem because traditional chemical precipitation does not remove all sulphates. In addition, it creates lime sediment as a secondary waste. Therefore, an inexpensive and environmental-friendly sulphate removal method is needed in addition to precipitation. In this study, carbon residues from a wood gasification process were repurposed as precursors to a suitable sorbent for SO42- ion removal. The raw material was modified using ZnCl2, BaCl2, CaCl2, FeCl3, or FeCl2. Carbon residues modified with FeCl3 were selected for further consideration because the removal efficiency toward sulphate was the highest. Batch sorption experiments were performed to evaluate the effects of the initial pH, initial SO42- ion concentration, and contact time on sulphate removal. The removal of SO42- ions using Fe-modified carbon residue was notably higher compared with unmodified carbon residue and commercially available activated carbon. The sorption data exhibited pseudo-second-order kinetics. The isotherm analysis indicated that the sorption data of Fe-modified carbon residues can be represented by the bi-Langmuir isotherm model.

Chemical sulphate removal for treatment of construction and demolition debris leachate.

Science.gov (United States)

Kijjanapanich, Pimluck; Annachhatre, Ajit P; Esposito, Giovanni; Lens, Piet N L

2014-08-01

Construction and demolition debris (CDD) is a product of construction, renovation or demolition activities. It has a high gypsum content (52.4% of total gypsum), concentrated in the CDD sand (CDDS) fraction. To comply with the posed limit of the maximum amount of sulphate present in building sand, excess sulphate needs to be removed. In order to enable reuse of CDDS, a novel treatment process is developed based on washing of the CDDS to remove most of the gypsum, and subsequent sulphate removal from the sulphate-rich CDDS leachate. This study aims to assess chemical techniques, i.e. precipitation and adsorption, for sulphate removal from the CDDS leachate. Good sulphate removal efficiencies (up to 99.9%) from the CDDS leachate can be achieved by precipitation with barium chloride (BaCl2) and lead(II) nitrate (Pb(NO3)2). Precipitation with calcium chloride (CaCl2), calcium carbonate (CaCO3) and calcium oxide (CaO) gave less efficient sulphate removal. Adsorption of sulphate to aluminium oxide (Al2O3) yielded a 50% sulphate removal efficiency, whereas iron oxide-coated sand as adsorbent gave only poor (10%) sulphate removal efficiencies.

Corrosion behaviour of a stream generator tube material in simulated steam generator feedwater containing chlorides and sulphates

Energy Technology Data Exchange (ETDEWEB)

Bojinov, M.; Kinnunen, P.; Laitinen, T.; Maekelae, K.; Saario, T.; Sirkiae, P.; Yliniemi, K. [VTT Manufacturing Technology, Espoo (Finland); Buddas, T.; Halin, M.; Tompuri, K. [Fortum Power and Heat Oy, Loviisa Power Plant (Finland)

2002-07-01

The goal of the present work has been to assess the effect of relatively high concentrations of anionic impurities (Cl{sup -}, SO{sub 4}{sup 2-}) on the corrosion behaviour of Ti-stabilised stainless steel SG tubes in simulated steam generator feed-water. The main observations of this work can be summarised as follows: Sulphate ions seem to be more aggressive than chloride ions towards the primary passive film on 08X18H10T stainless steel. The results may indicate that it is more important to have a low concentration of sulphate ions than of chloride ions in secondary side water when the effects of chemical conditions on tube degradation are considered. The presence of chloride ions seems to weaken the detrimental effect of sulphate ions on the stability of oxide films growing on 08X18H10T stainless steel. No localised corrosion features of 08X18H10T stainless steel were detected in the voltammetric and impedance measurements in solutions containing up to 5000 ppb sulphates, chlorides or both of the anions. (authors)

Corrosion behaviour of a stream generator tube material in simulated steam generator feedwater containing chlorides and sulphates

International Nuclear Information System (INIS)

Bojinov, M.; Kinnunen, P.; Laitinen, T.; Maekelae, K.; Saario, T.; Sirkiae, P.; Yliniemi, K.; Buddas, T.; Halin, M.; Tompuri, K.

2002-01-01

The goal of the present work has been to assess the effect of relatively high concentrations of anionic impurities (Cl - , SO 4 2- ) on the corrosion behaviour of Ti-stabilised stainless steel SG tubes in simulated steam generator feed-water. The main observations of this work can be summarised as follows: Sulphate ions seem to be more aggressive than chloride ions towards the primary passive film on 08X18H10T stainless steel. The results may indicate that it is more important to have a low concentration of sulphate ions than of chloride ions in secondary side water when the effects of chemical conditions on tube degradation are considered. The presence of chloride ions seems to weaken the detrimental effect of sulphate ions on the stability of oxide films growing on 08X18H10T stainless steel. No localised corrosion features of 08X18H10T stainless steel were detected in the voltammetric and impedance measurements in solutions containing up to 5000 ppb sulphates, chlorides or both of the anions. (authors)

Effect of chloride ions on the corrosion behavior of low-alloy steel containing copper and antimony in sulfuric acid solution

Science.gov (United States)

Park, Sun-Ah; Kim, Seon-Hong; Yoo, Yun-Ha; Kim, Jung-Gu

2015-05-01

The influence of the addition of HCl on the corrosion behavior of low-alloy steel containing copper and antimony was investigated using electrochemical (potentiodynamic and potentiostatic polarization tests, and electrochemical impedance spectroscopy) and weight loss tests in a 1.6M H2SO4 solution with different concentrations of hydrochloric acid (0.00, 0.08, 0.15 and 0.20 M HCl) at 60 °C. The result showed that the corrosion rate decreased with increasing HCl by the formation of protective layers. SEM, EDS and XPS examinations of the corroded surfaces after the immersion test indicated that the corrosion production layer formed in the solution containing HCl was highly comprised of metallic Cu, Cu chloride and metallic (Fe, Cu, Sb) compounds. The corrosion resistance was improved by the Cu-enriched layer, in which chloride ions are an accelerator for cupric ion reduction during copper deposition. Furthermore, cuprous and antimonious chloride species are complex salts for cuprous ions adsorbed on the surface during copper deposition.

[Concordance between the zinc sulphate flotation and centrifugal sedimentation methods for the diagnosis of intestinal parasites].

Science.gov (United States)

Inês, Elizabete De Jesus; Pacheco, Flavia Thamiris Figueiredo; Pinto, Milena Carneiro; Mendes, Patrícia Silva de Almeida; Da Costa-Ribeiro, Hugo; Soares, Neci Matos; Teixeira, Márcia Cristina Aquino

2016-12-01

The diagnosis of intestinal parasitic infections depends on the parasite load, the specific gravity density of the parasite eggs, oocysts or cysts, and the density and viscosity of flotation or sedimentation medium where faeces are processed. To evaluate the concordance between zinc sulphate flotation and centrifugal sedimentation in the recovery of parasites in faecal samples of children. Faecal samples of 330 children from day care centers were evaluated by zinc sulphate flotation and centrifugal sedimentation techniques. The frequencies of detection of parasites by each method were determined and the agreement between the diagnostic techniques was evaluated using the kappa index, with 95% confidence intervals. The faecal flotation in zinc sulphate diagnosed significantly more cases of Trichuris trichiura infection when compared to centrifugal sedimentation (39/330; 11.8% vs. 13/330; 3.9%, p<0.001), with low diagnostic concordance between methods (kappa=0.264; 95% CI: 0.102-0.427). Moreover, all positive samples for Enterobius vermicularis eggs (n=5) and Strongyloides stercoralis larvae (n=3) were diagnosed only by zinc sulphate. No statistical differences were observed between methods for protozoa identification. The results showed that centrifugal flotation in zinc sulphate solution was significantly more likely to detect light helminths eggs such as those of T. trichiura and E. vermicularis in faeces than the centrifugal sedimentation process.

Studies on Cementation of Tin on Copper and Tin Stripping from Copper Substrate

Directory of Open Access Journals (Sweden)

Rudnik E.

2016-06-01

Full Text Available Cementation of tin on copper in acid chloride-thiourea solutions leads to the formation of porous layers with a thickness dependent on the immersion time. The process occurs via Sn(II-Cu(I mechanism. Chemical stripping of tin was carried out in alkaline and acid solutions in the presence of oxidizing agents. It resulted in the dissolution of metallic tin, but refractory Cu3Sn phase remained on the copper surface. Electrochemical tin stripping allows complete tin removal from the copper substrate, but porosity and complex phase composition of the tin coating do not allow monitoring the process in unambiguous way.

Mesophilic leaching of copper sulphide sludge

Directory of Open Access Journals (Sweden)

VLADIMIR B. CVETKOVSKI

2009-02-01

Full Text Available Copper was precipitated using a sodium sulphide solution as the precipitation agent from an acid solution containing 17 g/l copper and 350 g/l sulphuric acid. The particle size of nearly 1 µm in the sulphide sludge sample was detected by optical microscopy. Based on chemical and X-ray diffraction analyses, covellite was detected as the major sulphide mineral. The batch bioleach amenability test was performed at 32 °C on the Tk31 mine mesophilic mixed culture using a residence time of 28 days. The dissolution of copper sulphide by direct catalytic leaching of the sulphides with bacteria attached to the particles was found to be worthy, although a small quantity of ferrous ions had to be added to raise the activity of the bacteria and the redox potential of the culture medium. Throughout the 22-day period of the bioleach test, copper recovery based on residue analysis indicated a copper extraction of 95 %, with copper concentration in the bioleach solution of 15 g/l. The slope of the straight line tangential to the exponential part of the extraction curve gave a copper solubilisation rate of 1.1 g/l per day. This suggests that a copper extraction of 95 % for the period of bioleach test of 13.6 days may be attained in a three-stage bioreactor system.

Standard specification for leak detector solutions intended for use on brasses and other copper alloys

CERN Document Server

American Society for Testing and Materials. Philadelphia

2005-01-01

1.1 This specification covers the requirements for leak detector solutions suitable for use in checking the leakage of valves, pipes, fittings, joints, and so forth of a pressurized gas system fabricated from brasses and other copper alloys. 1.2 This specification deals with the stress corrosion cracking aspect of leak detector solutions. The effectiveness, chemical, physical and mechanical properties of leak detector solutions are not within the scope of this specification. This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and to determine the applicability of regulatory limitations prior to use.

Copper(II) oxide solubility behavior in aqueous sodium phosphate solutions at elevated temperatures

International Nuclear Information System (INIS)

Ziemniak, S.E.; Jones, M.E.; Combs, K.E.S.

1990-02-01

A platinum-lined, flowing autoclave facility is used to investigate the solubility behavior of copper(II) oxide (CuO) in aqueous sodium phosphate solutions at temperatures between 292 and 535 K. Copper solubilities are observed to increase continuously with temperature and phosphate concentration. The measured solubility is examined via a Cu(II) ion hydrolysis/complexing model and thermodynamic functions for the hydrolysis/complexing reactions are obtained from a least- squares analysis of the data. Altogether, thermochemical properties are established for five anionic complexes: Cu(OH) 3 - , Cu(OH) 4 = , Cu(OH) 2 (HPO 4 ) = , Cu(OH) 3 (H 2 PO 4 ) = , and Cu(OH) 2 (PO 4 ) ≡ . Precise thermochemical parameters are also derived for the Cu(OH) + hydroxocomplex based on CuO solubility behavior previously observed in pure water (*) at elevated temperatures. The relative ease of Cu(II) ion hydrolysis is such that Cu(OH) 3 - species become the preferred hydroxocomplex for pH ≥ 9.4. 20 refs., 8 figs., 6 tabs

Incoloy 800 anodic behavior in sulfate and chloride solutions at high temperature

International Nuclear Information System (INIS)

Lafont, C.; Alvarez, M.G.

1992-01-01

The anodic behavior and pitting corrosion resistance of Incoloy 800 in concentrated aqueous chloride and sulphate solutions has been studied by means of electrochemical techniques. The effect of different environmental variables, such as temperature (in the 100 0 C to 280 0 C range) and sulphate ion concentration (0.02 M to 2 M), was evaluated. In another set of experiments, the influence of sulphate ions additions on the pitting resistance and pitting morphology of Incoloy 800 in chloride solutions at high temperature was also examined. (author)

Synthesis of Commercial Products from Copper Wire-Drawing Waste

Science.gov (United States)

Ayala, J.; Fernández, B.

2014-06-01

Copper powder and copper sulfate pentahydrate were obtained from copper wire-drawing scale. The hydrometallurgical recycling process proposed in this article yields a high-purity copper powder and analytical grade copper sulfate pentahydrate. In the first stage of this process, the copper is dissolved in sulfuric acid media via dismutation of the scale. In the second stage, copper sulfate pentahydrate is precipitated using ethanol. Effects such as pH, reaction times, stirring speed, initial copper concentration, and ethanol/solution volume ratio were studied during the precipitation from solution reaction. The proposed method is technically straightforward and provides efficient recovery of Cu from wire-drawing scale.

Removal of copper from aqueous solution by electrodeposition in cathode chamber of microbial fuel cell.

Science.gov (United States)

Tao, Hu-Chun; Liang, Min; Li, Wei; Zhang, Li-Juan; Ni, Jin-Ren; Wu, Wei-Min

2011-05-15

Based on energetic analysis, a novel approach for copper electrodeposition via cathodic reduction in microbial fuel cells (MFCs) was proposed for the removal of copper and recovery of copper solids as metal copper and/or Cu(2)O in a cathode with simultaneous electricity generation with organic matter. This was examined by using dual-chamber MFCs (chamber volume, 1L) with different concentrations of CuSO(4) solution (50.3 ± 5.8, 183.3 ± 0.4, 482.4 ± 9.6, 1007.9 ± 52.0 and 6412.5 ± 26.7 mg Cu(2+)/L) as catholyte at pH 4.7, and different resistors (0, 15, 390 and 1000 Ω) as external load. With glucose as a substrate and anaerobic sludge as an inoculum, the maximum power density generated was 339 mW/m(3) at an initial 6412.5 ± 26.7 mg Cu(2+)/L concentration. High Cu(2+) removal efficiency (>99%) and final Cu(2+) concentration below the USA EPA maximum contaminant level (MCL) for drinking water (1.3mg/L) was observed at an initial 196.2 ± 0.4 mg Cu(2+)/L concentration with an external resistor of 15 Ω, or without an external resistor. X-ray diffraction analysis confirmed that Cu(2+) was reduced to cuprous oxide (Cu(2)O) and metal copper (Cu) on the cathodes. Non-reduced brochantite precipitates were observed as major copper precipitates in the MFC with a high initial Cu(2+) concentration (0.1M) but not in the others. The sustainability of high Cu(2+) removal (>96%) by MFC was further examined by fed-batch mode for eight cycles. Copyright © 2011 Elsevier B.V. All rights reserved.

Calibration of brachytherapy sources using ferrous sulphate-benzoic acid-xylenol orange dosimeter

International Nuclear Information System (INIS)

Madhvanath, U.; Kini, U.R.; Gupta, B.L.

1976-01-01

A solution containing 0.20 mM of ferrous ammonium sulphate, 5.0 mM benzoic acid and 0.20 mM xylenol orange in 0.05 N sulphuric acid was used for the calibration of 252 Cf, 137 Cs, 226 Ra and 60 Co needle sources. A known volume of this solution contained in a pyrex glass tube was irradiated with the source kept in a glass capillary at the centre of the solution. A few hours of irradiation were required for each needle and the absorbance of the solution was measured at 540 nm against the unirradiated solution. The accuracy of this method was found to be within a few percent and is particularly useful for 252 Cf sources as the neutron component of the source contributes significantly to the absorbance produced. (author)

Sulphate Incorporation in Borosilicate Glasses and Melts: a Kinetic Approach

Energy Technology Data Exchange (ETDEWEB)

Lenoir, M. [CEA, DEN, Laboratoire d' etude et de Developpement de Matrices de Conditionnement, Centre de Marcoule, 30207 Bagnols-sur-Ceze (France); Physique des Mineraux et Magmas, UMR 7047, CNRS- Institut de Physique du Globe de Paris, 7 place Jussieu, 75252 Paris 05 (France); Grandjean, A. [Institut de Chimie Separative de Marcoule, UMR 5257, Laboratoire des Nanomateriaux Autoreparants, Marcoule, 30207 Bagnols-sur-Ceze (France); Dussossoy, J.L. [CEA, DEN, Laboratoire d' etude et de Developpement de Matrices de Conditionnement, Centre de Marcoule, 30207 Bagnols-sur-Ceze (France); Neuville, D.R. [Physique des Mineraux et Magmas, UMR 7047, CNRS- Institut de Physique du Globe de Paris, 7 place Jussieu, 75252 Paris 05 (France)

2008-07-01

The kinetics of sulphate departure in a sodium borosilicate melt were studied using in situ Raman spectroscopy. This technique allows the quantification of the amount of sulphate dissolved in a borosilicate glass as a function of heating time by comparison with measurements obtained by microprobe wavelength dispersive spectrometry. To quantify the sulphate content obtained with Raman spectroscopy, the integrated intensity of the sulphate band at 990 cm{sup -1} was scaled to the sum of the integrated bands between 800 and 1200 cm{sup -1}, bands that are assigned to Qn silica units on the basis of previous literature. Calibration curves were then determined for two different samples. An evaluation of the kinetics of departure of sulphate could thus be made as a function of the viscosity of the borosilicate glass, showing that the kinetics were controlled by the diffusion of sulphate and its volatilization from the melt. This experimental method allows in situ measurements of sulphate content at high temperature which cannot be obtained by any other simple technique. (authors)

Thermodynamic evaluation of Cu-H-O-S-P system - Phase stabilities and solubilities for OFP-copper

Energy Technology Data Exchange (ETDEWEB)

Magnusson, Hans; Frisk, Karin [Swerea KIMAB, Kista (Sweden)

2013-04-15

A thermodynamic evaluation for Cu-H-O-S-P has been made, with special focus on the phase stabilities and solubilities for OFP-copper. All binary systems including copper have been reviewed. Gaseous species and stoichiometric crystalline phases have been included for higher systems. Sulphur in OFP-copper will be found in sulphides. The sulphide can take different morphologies but constant stoichiometry Cu{sub 2}S. The solubility of sulphur in FCC-copper reaches ppm levels already at 550 deg C and decreases with lower temperature. No phosphorus-sulphide will be stable, although the copper sulphide can be replaced by copper sulphates at high partial pressure oxygen like in the oxide scale. Phosphorus has a high affinity to oxygen, and phosphorus oxide P{sub 4}O{sub 10} and copper phosphates (Cu{sub 2}P{sub 2}O{sub 7} and Cu{sub 3}(PO{sub 4}){sub 2}) are all more stable than copper oxide Cu{sub 2}O. With hydrogen present at atmospheric pressure, copper phosphates Cu{sub 2}P{sub 2}O{sub 7} and Cu{sub 3}(P{sub 2}O{sub 6}OH){sub 2} are both more stable than water vapour or aqueous water at temperatures below 400 deg C. At high pressure conditions, the copper phosphates can be reduced giving water. However, the phosphates are still more stable than water vapour. The solubility limit of phosphorus in FCC-copper at 25 deg C is 510 ppm, in equilibrium with copper phosphide Cu{sub 3}P. The major part of phosphorus in OFP-copper will be in solid solution. Oxygen in FCC-copper has a very low solubility. In the presence of a strong oxide forming element such as phosphorus in OFP-copper, the solubility decreases even more. Copper oxides will become stable first when all phosphorus has been consumed, which takes place at twice the phosphorus content, calculated in weight. Hydrogen has a low solubility in copper, calculated as 0.1 ppm at 675 deg C. No crystalline hydrogen phase has been found stable at atmospheric pressures and above 400 deg C. At lower temperatures the hydrogen

Extraction of sulphates by long chain amines; Extraction des sulfates par les amines a longues chaines

Energy Technology Data Exchange (ETDEWEB)

Boirie, Ch [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

1959-05-15

The extraction of sulphuric acid by long chain amines in organic solution has been studied with a view to determining the value of the stability constants of the amine sulphates and bi-sulphates formed. We have concentrated chiefly on uranium sulphate and thorium sulphate. The formulae of the complexes extractable with amines have been established, as well as the corresponding dissociation constants. We have observed that for uranium sulphate the formula of the complex depends only on the nature of the amine, whereas for thorium this formula varies with the amine structure. From the formulae determined and the value of the constants calculated, we have been able to establish the best conditions for uranium and thorium extraction and also for a separation of these two elements. Finally we propose an application of this study to the determination of uranium in ores, where the separation of uranium by this method is particularly easy and complete. (author) [French] L'extraction de l'acide sulfurique par des amines a longues chaines en solution organique a ete etudiee en vue de la determination de la valeur des constantes de stabilite des sulfates et bisulfates d'amines formes. Parmi les sulfates, nous nous sommes particulierement interesses au sulfate d'uranium et au sulfate de thorium. Nous avons determine les formules des complexes extractibles avec les amines, ainsi que les constantes de dissociation correspondantes. Nous avons remarque que pour le sulfate d'uranium, la formule du complexe ne depend que de la nature de l'amine, alors que pour le thorium cette formule varie avec la structure de l'amine. Les formules determinees et la valeur des constantes calculees, nous ont permis de decrire les meilleures conditions d'extraction de l'uranium et du thorium ainsi que celles d'une separation de ces deux elements. Nous proposons enfin une application de cette etude au dosage de l'uranium dans les minerais, ou la separation de l'uranium par cette methode est

Fabrication of Chitosan-complexed Electrode and Evaluation of Its Efficiency in Removal of Copper Ion from Aqueous Solution

Directory of Open Access Journals (Sweden)

Yoon Young-Chan

2016-01-01

Full Text Available In this study, we fabricated chitosan/PVA/activated carbon complexed electrode to remove copper ion from aqueous solution. The prepared composite electrode was analyzed by BET and SEM to investigate its physicochemical properties. Electrochemical properties of prepared composite electrodes were analyzed via cyclic voltammetry. Adsorption performance of copper ion on chitosan composite complexed electrodes was evaluated. Almost similar pore size distribution results were observed in the series of ACP not included electrodes while observed differences in pore size distribution for the ACP included one. Cyclic voltammetry results exhibited that oxidation-reduction reaction does not occur in a potential range of -1.0 ~ 1.0 V. The amount of copper ion during adsroption reaction is increase according to increase of adsorption potential to 1.0 V.

Gastrointestinal tract wall visualization and distention during abdominal and pelvic multidetector CT with a neutral barium sulphate suspension: comparison with positive barium sulphate suspension and with water.

Science.gov (United States)

Oliva, M R; Erturk, S M; Ichikawa, T; Rocha, T; Ros, P R; Silverman, S G; Mortele, K J

2012-01-01

When examining patients with contrast-enhanced multidetector-row CT, we determined if the stomach and small bowel were visualized and distended better with a neutral barium sulphate suspension than with positive barium sulphate suspension or water. After obtaining approval from our institutional review board, 156 patients (women: 84; mean age: 54 yrs) with no history of gastrointestinal tract disease were randomized prospectively to receive orally either 900 ml of neutral (0.1% w/v) barium sulphate suspension (n = 53), 900 ml of positive (2.1% w/v) barium sulphate suspension (n = 53), or 900 ml of water (n = 50), prior to undergoing contrast-enhanced abdominal and pelvic multidetector-row CT. Two independent radiologists evaluated the stomach, and small bowel, for luminal distension and wall visualization, using a five point scale. Results were compared using Kruskal-Wallis and Mann-Whitney U tests. The walls of the stomach, and small bowel were visualized better in patients who were administered neutral barium sulphate suspension than those who were administered either positive barium sulphate suspension (p barium sulphate suspension, the stomach and small bowel were distended better compared to patients administered water (p barium sulphate suspension (p contrast-enhanced abdominal and pelvic multidetector-row CT, orally administered neutral barium sulphate suspension allows the gastrointestinal tract to be visualized and distended better than either positive barium sulphate suspension, or water.

Effects of agmatine sulphate on facial nerve injuries.

Science.gov (United States)

Surmelioglu, O; Sencar, L; Ozdemir, S; Tarkan, O; Dagkiran, M; Surmelioglu, N; Tuncer, U; Polat, S

2017-03-01

To evaluate the effect of agmatine sulphate on facial nerve regeneration after facial nerve injury using electron and light microscopy. The study was performed on 30 male Wistar albino rats split into: a control group, a sham-treated group, a study control group, an anastomosis group, and an anastomosis plus agmatine sulphate treatment group. The mandibular branch of the facial nerve was dissected, and a piece was removed for histological and electron microscopic examination. Regeneration was better in the anastomosis group than in the study control group. However, the best regeneration findings were seen in the agmatine sulphate treatment group. There was a significant difference between the agmatine group and the others in terms of median axon numbers (p Agmatine sulphate treatment with anastomosis in traumatic facial paralysis may enhance nerve regeneration.

Influence of Valsartan on the thermodynamics of micellization of anionic surfactant Sodium Dodecyl Sulphate

Directory of Open Access Journals (Sweden)

Stopková L.

2016-12-01

Full Text Available In this manuscript was investigated behaviour of drug valsartan by micellar media of anionic surfactant sodium dodecyl sulphate. As the method was used electrical conductivity for the determination of critical micelle concentration at different temperatures (T = 293.15 - 313.15 K, as well as calculated thermodynamic parameters like standard Gibbs free energy, enthalpy and entropy of micellization. According to contribution of Gibbs free energy is the process of micellization primarily controlled by entropy. Solubilization of valsartan was studied in surfactant system at 298.15 K and physiological conditions pH 7.4 using UV-spectrophotometry at different concentration range (0.001 - 0.07 mol/l of sodium dodecyl sulphate. The solubilization of drug was observed with increasing concentration of surfactant in aqueous solution.

Anthropogenic influence on the distribution of tropospheric sulphate aerosol

Energy Technology Data Exchange (ETDEWEB)

Langner, J; Rodhe, H; Crutzen, P J; Zimmermann, P [Swedish Meteorological and Hydrological Institute, Norrkoeping (Sweden)

1992-10-22

Human activities have increased global emissions of sulphur gases by about a factor of three during the past century, leading to increased sulphate aerosol concentrations, mainly in the Northern Hemisphere. Sulphate aerosols can affect the climate directly, by increasing the backscattering of solar radiation in cloud-free air, and indirectly, by providing additional cloud condensation nuclei. Here a global transport-chemistry model is used to estimate the changes in the distribution of tropospheric sulphate aerosol and deposition of non-seasalt sulphur that have occurred since pre-industrial times. The increase in sulphate aerosol concentration is small over the Southern Hemisphere oceans, but reaches a factor of 100 over northern Europe in winter. Calculations indicate, however, that at most 6% of the anthropogenic sulphur emissions is available for the formation of new aerosol particles. This is because about one-half of the sulphur dioxide is deposited on the Earth's surface, and most of the remainder is oxidized in cloud droplets so that the sulphate becomes associated with pre-existing particles. Even so, the rate of formation of new sulphate particles may have doubled since pre-industrial times. 18 refs., 3 figs.

A novel aggregation induced emission active cyclometalated Ir(III) complex as a luminescent probe for detection of copper(II) ion in aqueous solution

Energy Technology Data Exchange (ETDEWEB)

Shen, Wei; Yan, Liqiang; Tian, Wenwen; Cui, Xia; Qi, Zhengjian, E-mail: qizhengjian@seu.edu.cn; Sun, Yueming, E-mail: sun@seu.edu.cn

2016-09-15

We report the synthesis and characterization of a novel aggregation induced emission (AIE) active cyclometalated Ir(III) complex, namely [Ir(dfppy){sub 2}(phen-DPA)]PF{sub 6}, where dfppy and phen-DPA represent 2-(2,4-difluorophenyl)pyridine and 2-(bis(pyridin-2-ylmethyl)amino)-N-(1,10-phenanthrolin-5-yl)acetamide, respectively. The complex showed remarkable selectivity for copper(II) in aqueous solution over other competitive ions. Furthermore, this sensor showed a rapid and reversible response to copper(II) in aqueous solution with a detection limit of 65 nM.

Response of solute and precipitation-strengthened copper alloys at high neutron exposure

International Nuclear Information System (INIS)

Garner, F.A.; Hamilton, M.L.; Shikama, T.; Edwards, D.J.; Newkirk, J.W.

1991-11-01

A variety of solute and precipitation strengthened copper base alloys have been irradiated to neutron-induced displacement levels of 34 to 150 dpa at 415 degrees C and 32 dpa at 529 degrees C in the Fast Flux Test Facility to assess their potential for high heat flux applications in fusion reactors. Several MZC-type alloys appear to offer the most promise for further study. For low fluence applications CuBeNi and spinodally strengthened CuNiTi alloys may also be suitable. Although Cu-2Be resists swelling, it is not recommended for fusion reactor applications because of its low conductivity

Response of solute and precipitation-strengthened copper alloys at high neutron exposure

Energy Technology Data Exchange (ETDEWEB)

Garner, F.A.; Hamilton, M.L. [Pacific Northwest Lab., Richland, WA (United States); Shikama, T. [Tohoku Univ., Oarai Branch (Japan); Edwards, D.J.; Newkirk, J.W. [Missouri Univ., Rolla, MO (United States)

1991-11-01

A variety of solute and precipitation strengthened copper base alloys have been irradiated to neutron-induced displacement levels of 34 to 150 dpa at 415{degrees}C and 32 dpa at 529{degrees}C in the Fast Flux Test Facility to assess their potential for high heat flux applications in fusion reactors. Several MZC-type alloys appear to offer the most promise for further study. For low fluence applications CuBeNi and spinodally strengthened CuNiTi alloys may also be suitable. Although Cu-2Be resists swelling, it is not recommended for fusion reactor applications because of its low conductivity.

Sequential Determination of Total Arsenic and Cadmium in Concentrated Cadmium Sulphate Solutions by Flow-Through Stripping Chronopotentiometry after Online Cation Exchanger Separation

Directory of Open Access Journals (Sweden)

Frantisek Cacho

2012-01-01

Full Text Available Flow-through stripping chronopotentiometry with a gold wire electrode was used for the determination of total arsenic and cadmium in cadmium sulphate solutions for cadmium production. The analysis is based on the online separation of arsenic as arsenate anion from cadmium cations by means of a cation exchanger. On measuring arsenate in the effluent, the trapped cadmium is eluted by sodium chloride solution and determined in a small segment of the effluent by making use of the same electrode. The elaborated protocol enables a full automatic measurement of both species in the same sample solution. The accuracy of the results was confirmed by atomic absorption spectrometry. The LOD and LOQ for Arsenic were found to be 0.9 μg dm-3 and 2.7 μg dm-3, respectively. A linear response range was observed in the concentration range of 1 to 300 μg dm-3 for sample volumes of 4 mL. The repeatability and reproducibility were found to be 2.9% and 5.2%, respectively. The linear response range for cadmium was found to be 0.5 to 60 g/L. The method was tested on samples from a cadmium production plant.

Controlling Barium Sulphate Scale Deposition Problems in an unbleached Kraft Paper Mill

CSIR Research Space (South Africa)

Sithole, Bruce

2015-06-01

Full Text Available Troubleshooting of scale deposits and defects in paper samples showed that the problem was caused by barium sulphate and calcium sulphate scales. However, it was ascertained that barium sulphate was more of a concern than calcium sulphate...

Kinetics of barium sulphate reaction crystallization in crystallizers with internal circulation

Directory of Open Access Journals (Sweden)

J. Koralewska

2008-06-01

Full Text Available Kinetic calculation results describing the observed nucleation and growth rates of barium sulphate crystals precipitated in an integrated reaction-crystallization process in a barium sulphate-ammonium chloride-water system are presented and analyzed. The scope of experiments included two continuous model DTM-type crystallizers (Draft Tube Magma with internal circulation of the suspension forced by a liquid jet-pump device responsible for stable and intensive enough ascending/descending flow of BaSO4 crystal magma in a mixing chamber. For comparison purposes the experimental data corresponding to a continuous DT (Draft Tube crystallizer with propeller agitator are presented and discussed. The various types of laboratory crystallizers used were fed with concentrated water solution of barium chloride (of 10 or 24 mass % and - in a stoichiometric proportion - crystalline ammonium sulphate, assuming isothermal (348 K and hydrodynamic (average residence time of suspension in a crystallizer: 900 s process conditions. The observed nucleation and growth rates of barium sulphate crystals were estimated on the basis of crystal size distributions (CSDs using convenient calculation scheme derived for an MSMPR (Mixed Suspension Mixed Product Removal model approach. Considering the experimental population density distribution courses, a size-dependent growth (SDG phenomenon was taken into account in the kinetic calculations. Five SDG kinetic models recommended in the accessible literature were used for kinetic parameter values estimation. It was proved statistically, that Rojkowski’s two SDG models (hyperbolic and exponential best suit for our own experimental data description. The experimental data presented can be practically applied for improving the constructions of liquid jet-pump DTM crystallizers recommended for reaction crystallization of sparingly soluble inorganic salts (especially for high concentrations of reaction substrates in the modern

Treatment with magnesium sulphate in pre-term birth

DEFF Research Database (Denmark)

Wolf, Hans; Hegaard, H K; Greisen, G

2012-01-01

Premature birth increases a child's risk of cerebral palsy and death. The aim of this work is to investigate the association between treatment with magnesium sulphate during premature deliveries and infants' cerebral palsy and mortality through a meta-analysis of observational studies....... A comprehensive search of the Cochrane Library, EMBASE and the PubMed database from their inceptions to 1 October, 2010 using the keywords 'magnesium sulphate, children/infant/pre-term/premature and cerebral palsy/mortality/morbidity/adverse effects/outcome' identified 11 reports of observational studies. Two...... authors working independently extracted the data. A meta-analysis of the data found an association between magnesium sulphate treatment and a significantly reduced risk of mortality (RR 0.73; 95% CI 0.61-0.89) and cerebral palsy (OR 0.64; 95% CI 0.47-0.89). Antenatal treatment with magnesium sulphate...

Tetrachloroethylene Removal Rate from Aqueous Solutions by Pumice Doped with Copper: An Evaluation of the Effect of pH

Directory of Open Access Journals (Sweden)

Ali Almasi

2016-12-01

Full Text Available Tetrachloroethylene (TCE is a chlorinated aliphatic hydrocarbon, used in many industries. Effective and efficient treatment of industrial wastewater, containing TCE, is one of the environmental requirements. The purpose of this study was to determine the role of alkaline environments in TCE removal rate from aqueous solutions, using copper-doped pumice. This experimental study was performed, using granulated pumice stones with a mesh 4 (8.4 mm in alkaline conditions; the samples were coated with copper. Copper-doped pumice was prepared as a bed at doses of 1, 2, and 3 g/L; the study was performed at pH ranges of 3, 7, and 11. Based on the results, copper-doped pumice showed good efficacy in TCE removal; in addition, its performance increased in alkaline conditions. Therefore, use of this stone for the treatment of wastewater, containing TCE, is effective due to its availability and low cost. Besides, it can be considered a good option, given its high efficiency in the absorption process.

Al-Fe interactions and growth enhancement in Melastoma malabathricum and Miscanthus sinensis dominating acid sulphate soils.

Science.gov (United States)

Watanabe, Toshihiro; Jansen, Steven; Osaki, Mitsuru

2006-12-01

Plants growing in acid sulphate soils are subject to high levels of Al availability, which may have effects on the growth and distribution of these species. Although Fe availability is also high in acid sulphate soils, little is known about the effect of Fe on the growth of native plants in these soils. Two species dominating this soil type in Asia, viz. Melastoma malabathricum and Miscanthus sinensis were grown hydroponically in a nutrient solution with different concentrations of Al and Fe. Melastoma malabathricum is found to be sensitive to Fe (40 and 100 microm). Application of 500 microm Al, however, completely ameliorates Fe toxicity and is associated with a decrease of Fe concentration in shoots and roots. The primary reason for the Al-induced growth enhancement of M. malabathricum is considered to be the Al-induced reduction of toxic Fe accumulation in roots and shoots. Therefore, Al is nearly essential for M. malabathricum when growing in acid sulphate soils. In contrast, application of both Fe and Al does not reduce the growth of M. sinensis, and Al application does not result in lower shoot concentrations of Fe, suggesting that this grass species has developed different mechanisms for adaptation to acid sulphate soils.

Sulphate in Liquid Nuclear Waste: from Production to Containment

Energy Technology Data Exchange (ETDEWEB)

Lenoir, M.; Grandjean, A.; Ledieu, A.; Dussossoy, J.L.; Cau Dit Coumes, C.; Barre, Y.; Tronche, E. [CEA Marcoule, DEN/DTCD/SECM/LDMC, Batiment 208 BP17171, Bagnols sur Ceze, 30207 (France)

2009-06-15

Nuclear industry produces a wide range of low and intermediate level liquid radioactive wastes which can include different radionuclides such as {sup 90}Sr. In La Hague reprocessing plant and in the nuclear research centers of CEA (Commissariat a l'Energie Atomique), the coprecipitation of strontium with barium sulphate is the technique used to treat selectively these contaminated streams with the best efficiency. After the decontamination process, low and intermediate level activity wastes incorporating significant quantities of sulphate are obtained. The challenge is to find a matrix easy to form and with a good chemical durability which is able to confine this kind of nuclear waste. The current process used to contain sulphate-rich nuclear wastes is bituminization. However, in order to improve properties of containment matrices and simplify the process, CEA has chosen to supervise researches on other materials such as cements or glasses. Indeed, cements are widely used for the immobilization of a variety of wastes (low and intermediate level wastes) and they may be an alternative matrix to bitumen. Even if Portland cement, which is extensively used in the nuclear industry, presents some disadvantages for the containment of sulphate-rich nuclear wastes (risk of swelling and cracking due to delayed ettringite formation), other cement systems, such as calcium sulfo-aluminate binders, may be valuable candidates. Another matrix to confine sulphate-rich waste could be the glass. One of the advantages of this material is that it could also immobilize sulphate containing high level nuclear waste which is present in some countries. This waste comes from the use of ferrous sulfamate as a reducing agent for the conversion of Pu{sup 4+} to Pu{sup 3+} in the partitioning stage of the actinides during reprocessing. Sulphate solubility in borosilicate glasses has already been studied in CEA at laboratory and pilot scales. At a pilot scale, low level liquid waste has been

Uranium accompanying recovery from copper ores

International Nuclear Information System (INIS)

Golynko, Z.Sh.; Laskorin, B.N.

1981-01-01

In the search for new raw material sources for nuclear power engineering a review of the technique of uranium accompaning recovery from copper ores reprocessing products in some countries is presented. In the USA a sorption method of uranium extraction by means of strongly basic ion exchange resins from solutions upon copper case- hardening with subsequent extraction from eluates by solutions of tertiary amines is realized. Elution is realized with sulphuric acid. In South Africa an extraction reprocessing of gravitational concentrate extracted from copper sulphide flotation tailings is organized. In India the uranium extraction from copper ores flotation enrichment tailings is organized on a commerical scale. Presented are data on the scale of uranium recovery, various conditions of its recovery as well as block diagrams of the processes. It is shown that copper ores become an additional source of uranium recovery [ru

Post traumatic tetanus and role magnesium sulphate

International Nuclear Information System (INIS)

Sikendr, R.I.; Samad, B.U.; Memon, M.I.

2009-01-01

Tetanus is a life threatening disease. Reported mortality for tetanus is 15-39%. Conventional treatment includes heavy sedation and artificial ventilation. Complications resulting from long term heavy sedation and artificial ventilation contribute to 60% of the total mortality caused by tetanus. In this study magnesium sulphate was used to reduce the need for sedation and artificial ventilation. Objectives of this prospective study were to determine the role of magnesium sulphate in post traumatic tetanus. The study was carried out in surgical Intensive Care at Pakistan Institute of Medical Sciences (PIMS), Islamabad from Jan 2004 to Dec 2007. Forty-four patients presented during this period and 33 patients were included in the study. All patients had tracheostomy done within 48 hours. Every patient was started Magnesium Sulphate therapy for control of spasms after sending baseline investigations. Patients were given ventilatory support when needed. All data was entered in well structured proforma. SPSS-10 was used to analyse data. Thirty-three patients were included in the study and all patients were given magnesium sulphate. Out of these, 45.5% cases were grade 4 tetanus, 73.6% and 63.3% cases did not require artificial ventilation and additional sedation respectively, 51.1% patients remained free of complications of tetanus. Overall mortality was 30.3%. Use of Magnesium Sulphate is safe and reduces the need for sedation and artificial ventilation in high grade tetanus thus contributing to survival benefit in adult post-traumatic tetanus cases. (author)

Copper Deficiency Leads to Anemia, Duodenal Hypoxia, Upregulation of HIF-2α and Altered Expression of Iron Absorption Genes in Mice

Science.gov (United States)

Matak, Pavle; Zumerle, Sara; Mastrogiannaki, Maria; El Balkhi, Souleiman; Delga, Stephanie; Mathieu, Jacques R. R.; Canonne-Hergaux, François; Poupon, Joel; Sharp, Paul A.; Vaulont, Sophie; Peyssonnaux, Carole

2013-01-01

Iron and copper are essential trace metals, actively absorbed from the proximal gut in a regulated fashion. Depletion of either metal can lead to anemia. In the gut, copper deficiency can affect iron absorption through modulating the activity of hephaestin - a multi-copper oxidase required for optimal iron export from enterocytes. How systemic copper status regulates iron absorption is unknown. Mice were subjected to a nutritional copper deficiency-induced anemia regime from birth and injected with copper sulphate intraperitoneally to correct the anemia. Copper deficiency resulted in anemia, increased duodenal hypoxia and Hypoxia inducible factor 2α (HIF-2α) levels, a regulator of iron absorption. HIF-2α upregulation in copper deficiency appeared to be independent of duodenal iron or copper levels and correlated with the expression of iron transporters (Ferroportin - Fpn, Divalent Metal transporter – Dmt1) and ferric reductase – Dcytb. Alleviation of copper-dependent anemia with intraperitoneal copper injection resulted in down regulation of HIF-2α-regulated iron absorption genes in the gut. Our work identifies HIF-2α as an important regulator of iron transport machinery in copper deficiency. PMID:23555700

Treatment of model and galvanic waste solutions of copper(II) ions using a lignin/inorganic oxide hybrid as an effective sorbent.

Science.gov (United States)

Ciesielczyk, Filip; Bartczak, Przemysław; Klapiszewski, Łukasz; Jesionowski, Teofil

2017-04-15

A study was made concerning the removal of copper(II) ions from model and galvanic waste solutions using a new sorption material consisting of lignin in combination with an inorganic oxide system. Specific physicochemical properties of the material resulted from combining the activity of the functional groups present in the structure of lignin with the high surface area of the synthesized oxide system (585m 2 /g). Analysis of the porous structure parameters, particle size and morphology, elemental composition and characteristic functional groups confirmed the effective synthesis of the new type of sorbent. A key element of the study was a series of tests of adsorption of copper(II) ions from model solutions. It was determined how the efficiency of the adsorption process was affected by the process time, mass of sorbent, concentration of adsorbate, pH and temperature. Potential regeneration of adsorbent, which provides the possibility of its reusing and recovering the adsorbed copper, was also analyzed. The sorption capacity of the material was measured (83.98mg/g), and the entire process was described using appropriate kinetic models. The results were applied to the design of a further series of adsorption tests, carried out on solutions of real sewage from a galvanizing plant. Copyright © 2017 Elsevier B.V. All rights reserved.

Method for determining microamounts of uranium in solutions from copper ores, by liquid-liquid extraction and spectrophotometry with arsenazo III

International Nuclear Information System (INIS)

Rodriguez, B.

1972-01-01

A spectrophotometric method is described for determining small amounts of uranium in aqueous solutions from copper ores. Uranium is quantitatively separated in a single extraction by a solution of tri-n-octylphosphine oxide in benzene, using ethylendiaminetetracetic acid and sodium fluoride as complexing agents, for improving the selectivity of the procedure. An aliquot of the extract is diluted with a hydrocolloidal solution of arsenazo III. Optical density is measured at 650 nm. (Author) 3 refs

Potassium sorbate-A new aqueous copper corrosion inhibitor

International Nuclear Information System (INIS)

Abelev, Esta; Starosvetsky, David; Ein-Eli, Yair

2007-01-01

This work presents the novel nature of 2,4-hexadienoic acid potassium salt (potassium sorbate (KCH 3 CH=CHCH=CHCO 2 )) as an effective copper aqueous corrosion inhibitor. The influence of pH and potassium sorbate concentration on copper corrosion in aerated sulfate and chloride solutions is reported. Degree of copper protection was found to increase with an increase in potassium sorbate concentration; an optimum concentration of this inhibitor in sulfate solutions was found to be 10 g/L. Copper is highly resistant to corrosion attacks by chloride ions in the presence of potassium sorbate. X-ray photoelectron spectroscopy (XPS) studies suggest that copper protection is achieved via the formation of a mixed layer of cuprous oxide, cupric hydroxide and copper(II)-sorbate at the metal surface

Effects of Cuminum cyminum L. essential oil on some epididymal sperm parameters and histopathology of testes following experimentally induced copper poisoning in mice.

Science.gov (United States)

Sakhaee, E; Emadi, L; Azari, O; Kheirandish, R; Esmaili Nejad, M R; Shafiei Bafti, H

2016-06-01

Copper overload can cause sperm cell damage by inducing oxidative stress. On the other hand, cumin has a good antioxidant potential. Therefore, the aim of this study was to evaluate the effects of cumin on sperm quality and testicular tissue following experimentally induced copper poisoning in mice. Forty-eight mature male mice were divided into four equal groups as follows: group Cu which received 0.1 ml copper sulphate at dose of 100 mg kg(-1) , group Cc which received Cuminum cyminum at dose of 1 mg kg(-1) , treatment group which received copper sulphate (100 mg kg(-1) ) and treated with Cuminum cyminum (1 mg kg(-1) ), and control group which received the same volume of normal saline. Six mice in each group were sacrificed at week 4 and week 6. The results showed that sperm concentration, motility and viability in group Cu were significantly decreased at weeks 4 and 6, and severe degenerative changes were observed in testicular tissues in comparison with the control group. In treatment group, significant improvement in the sperm count, motility and viability, and normal architecture in most seminiferous tubules with organised epithelium was observed compared to the group Cu. The sperm quality parameters in the treatment group approached those of the control group. © 2015 Blackwell Verlag GmbH.

Interdependent action of nickel sulphate and X-rays on human lymphoblastoid leukeamic cells

International Nuclear Information System (INIS)

Bensimon, Jacques

1977-01-01

In a first experiment, cells were cultured in media supplemented by nickel sulphate, irradiated in same media and cultured in same media after irradiation. In a second experiment, cells were cultured during 18hrs. in media supplemented by nickel sulphate, and then cells were washed and cultured in normal media where they were irradiated. The nickel sulphate toxicity appears as a creasing function of the nickel sulphate concentration and the nickel sulphate action endurance. The nickel sulphate toxic effect is amplified by X-rays. This amplification is a time function that depends on the X-ray dose, nickel sulphate concentration and period of time from the outset of culture to the irradiation. The nickel sulphate toxic effect appears faster when nickel works after X-rays [fr

Critical parameters in the dump and heap leaching of gold, silver, copper and uranium: permeability, solution delivery and solution recovery

Energy Technology Data Exchange (ETDEWEB)

Lastra, M.K.; Chase, C.K.

1984-02-01

Critical to successful dump and heap leaching for gold, silver, copper and uranium are factors such as permeability, solution delivery to the ore, and solution recovery. This paper deals with possible techniques for successful accomplishment of these three factors. New developments as well as older techniques are discussed, together with rationals for use of some techniques in reference to others. The authors hope to present a checklist so that the ideal application to individual mine situations can be achieved. This involves a discussion of the merits of each different method and the situations for most logical application. It is hoped that such discussion will broaden the geographic areas where dump and heap leaching can be applied to include greater winter cold and tropical regions of large amounts of rainfall.

Critical parameters in the dump and heap leaching of gold, silver, copper and uranium: permeability, solution delivery and solution recovery

International Nuclear Information System (INIS)

Lastra, M.K.; Chase, C.K.

1984-01-01

Critical to successful dump and heap leaching for gold, silver, copper and uranium are factors such as permeability, solution delivery to the ore, and solution recovery. This paper deals with possible techniques for successful accomplishment of these three factors. New developments as well as older techniques are discussed, together with rationals for use of some techniques in reference to others. The authors hope to present a checklist so that the ideal application to individual mine situations can be achieved. This involves a discussion of the merits of each different method and the situations for most logical application. It is hoped that such discussion will broaden the geographic areas where dump and heap leaching can be applied to include greater winter cold and tropical regions of large amounts of rainfall

Detoxification of copper fungicide using EDTA-modified cellulosic ...

African Journals Online (AJOL)

STORAGESEVER

2009-02-04

Feb 4, 2009 ... Different countries or states have different laws, thus, ... fungi is due to the toxicity of copper ions in solution. A variety of copper .... initial concentration of Cu(II) ion solution, which ranged from 1400 to ..... exchange mechanism.

Leaching of copper concentrates using NaCl and soluble copper contributed by the own concentrate

International Nuclear Information System (INIS)

Herrero, O.; Bernal, N.; Quiroz, R.; Fuentes, G.; Vinals, J.

2005-01-01

Leaching of copper concentrates using cupric chloro complexes, generated in situ by the reaction between Cu(II), aported by the soluble copper content of the concentrate, and sodium chloride in acid media was studied. The concentrate samples were obtained from mineral processing plants from Antofagasta, Chile. Chemical and mineralogical characterization from original concentrates was made. Typical variable such as a chloride concentration, soluble copper concentration, leaching time, solid percentage and temperature were studied. DRX and EDS analyzed some of the residues. the experimental results indicated that it is possible to obtain solutions having high copper content (15 to 35 g/L) and 2 to 5 g/L free acid in order to submit this solution directly to a solvent extraction stage. The leaching tests use common reactive and low cost such as sodium chloride and sulfuric acid. (Author) 16 refs

Study of the process of multistage leaching of alum shale's sulphate d ashes

International Nuclear Information System (INIS)

Maremae, E.; Ruendal, L.; Ahelik, V.

1991-01-01

The scheme of the process was worked out on the basis of small (the weight of starting ashes 1 kg) and big (76.2 kg) laboratory tests with the result of getting aluminium potassium sulphate (alum) as a commercial product, and a technological solution with increased content of metals (Ti, Mo, V, U, etc.). Ashes received by means of Toolse deposit (Estonia) alum-shale fluidized-bed ashing at 800 o C, were used as basic material. The ashes were sulphate d in combustion tubes provided with electric heater using sulphate roasting process: the ashes were mixed with 75% H 2 SO 4 with the ratio S : L = 4 : 3 to get a homogeneous paste which was calcinated in the tube at 250-300 o C for 30 min. The calcinated paste (clinker) was treated with boiling water. The leaching experiments were carried out with various S : L ratios; in small test - in 2-litre bulbs, equipped with a stirring-rod, reflux condenser and thermometer, in the pulp at boiling temperature (101 o C). The hot leaching pulp was filtered under pressure using forcing filters. The final solutions were cooled and treated in order to receive alum. Under the conditions of a discontinuous process, the yield of raw alum (content of Fe 2 O 3 ∼1%) made up 240-270 kg/t of the starting ashes, both at the expense of the ashes' own potassium and at the expense of the potassium added from outside. The standard alum with regard to the content of iron admixture was obtained after repeated recrystallization of the raw alum. After the separation of alum, the solutions with the specific weight of 1.4-1.5 t/m 3 , and with the following average metal and sulphuric acid content in the solutions of the small and big tests were obtained: Ti 4.8 and 8.3; Mo 0.4 and 0.8; V 1.0 and 1.9; U 0.2 and 0.5; Fe 66 and 90; Al 18 and 20; K 1.9 and 3.4; H 2 SO 4 117 and 123 g/l, respectively. The extraction of metals into the solution in small and big tests was as follows: ti 71 and 64, Mo 73 and 66, V94 and 86, U 91 and 77, Fe 69 and 60, Al 45

Distribution of sulphur isotopes of sulphates in groundwaters from the principal artesian aquifer of Florida and the Edwards aquifer of Texas, United States of America

International Nuclear Information System (INIS)

Rightmire, C.T.; Pearson, F.J. Jr.; Back, W.; Rye, R.O.; Hanshaw, B.B.

1974-01-01

New information on the sources of sulphate dissolved in groundwater is obtainable from the measurement of the sulphur isotope composition of sulphates. Field studies in the Floridan aquifer, Florida, and the Edwards aquifer, Texas, show that the use of sulphur isotope data in conjunction with hydrologic and geochemical techniques permits refinements of interpretation. In the Floridan the interpretation of the chemical data, particularly the SO 4 2- concentration and the SO 4 2- /Cl - ratio, leads to the conclusion that recharging maritime rainfall, solution of intraformational gypsum, and mixing with ocean-like saline waters are the sources of sulphate in the groundwater. Sulphur isotope data substantiate this interpretation. The Edwards in the area studied can be separated into two hydrologie units on the basis of water chemistry and aquifer characteristics. The sulphide-free waters in the part of the aquifer upgradient from a distinct sulphide boundary are low in sulphate (less than 100 mg/1) and contain no sulphide. The waters downgradient from that boundary contain greater than 150 mg/1 sulphate and all contain measurable quantities of sulphide. Interpretation of the SO 4 2- concentration and SO 4 2- /Cl ratio on the basis of the Florida study leads to the erroneous conclusion that the solution of intraformational gypsum is again a major source of sulphate in the sulphide-free part of the aquifer. Isotope analyses, however, show that the gypsum is likely to be Permian in age and introduced into the aquifer by the recharge water. The absence of evidence for enrichment in 34 S in the sulphate in the sulphide-bearing portion of the aquifer leads to the possibility of H 2 S migration upgradient from downdip oil fields. (author)

Removal of copper (II) from aqueous solutions by adsorption onto granular activated carbon in the presence of competitor ions

International Nuclear Information System (INIS)

Almohammadi, S.; Mirzaei, M.

2016-01-01

In this work, the removal of copper from an aqueous solution by granular activated carbon (GAC) in the presence of competitor ions was studied. A batch adsorption was carried out and different parameters such as p H, contact time, initial copper concentration and competitor ions concentration were changed to determine the optimum conditions for adsorption. The optimum p H required for maximum adsorption was found to be 4.5 for copper. Equilibrium was evaluated at 144 h at room temperature. The removal efficiency of Cu(II) was 71.12% at this time. The kinetics of copper adsorption on activated carbon followed the pseudo second-order model. The experimental equilibrium sorption data were tested using the Langmuir, Freundlich, Temkin and Dubinin–Radushkevich (D-R) equations and the Langmuir model was found to be well fitted for copper adsorption onto GAC. The maximum adsorption capacity of the adsorbent for Cu(II) was calculated from the Langmuir isotherm and found to be 7.03 mg/g. Subsequently, the removal of copper by granular activated carbon in the presence of Ag 1 + and Mn 2 + as competitor ions was investigated. The removal efficiency of Cu(II) ions without the presence of the competitor ions was 46% at 6 h, while the removal efficiency of Cu(II) ions in the presence of competitor ions, Ag 1 + and Mn 2 + , was 34.76% and 31.73%, respectevely.

Mesophilic and thermophilic anaerobic digestion of sulphate-containing wastewaters.

Science.gov (United States)

Colleran, E; Pender, S

2002-01-01

The effect of sulphate at an influent chemical oxygen demand (COD):sulphate ratio of 4 on the operational performance of anaerobic hybrid reactors treating molasses wastewater was investigated under mesophilic and thermophilic conditions in a long-term laboratory-scale study over a 1,081 day period. The presence of sulphate reduced the COD removal efficiency under both mesophilic and thermophilic conditions. At 55 degrees C, effluent acetate levels were consistently greater than 4000 mg l(-1) indicating that thermophilic acetate-utilising methane-producing bacteria (MPB) or sulphate-reducing bacteria (SRB) had not developed in the reactor under the conditions applied. At 37 degrees C, acetate was exclusively utilised by acetoclastic methanogens, whereas H2-utilising SRB predominated over H2-utilising MPB in the competition for hydrogen. By contrast, hydrogenotrophic MPB were shown to outcompete H2-utilising SRB during long-term thermophilic operation. 16SrDNA analysis of the seed sludge and reactor biomass on conclusion of the 37 degrees C and 55 degrees C trials illustrated that the dominant methanogen present on conclusion of the thermophilic trial in the absence of influent sulphate was related to Methanocorpusculum parvuum, and was capable of growth on both acetate and hydrogen. By contrast, an organism closely related to Methanobacterium thermoautotrophicum was the dominant methanogen present in the sulphate-fed reactor on completion of the thermophilic trial.

The electrochemical atomic layer deposition of Pt and Pd nanoparticles on Ni foam for the electro oxidation of alcohols

CSIR Research Space (South Africa)

Modibedi, RM

2013-01-01

Full Text Available procedure The chemicals used in the preparation were Platinum solution (1mM H2PtCl6 pH = 1, SA Precious Metals), Pd solution (1mM PdCl2 pH = 1, SA Precious Metals), (copper sulphate solution (1mM CuSO4.5H2O pH = 1, Merck) were prepared in perchloric...

Toxicity of algal-derived aldehydes to two invertebrate species: Do heavy metal pollutants have a synergistic effect?

Energy Technology Data Exchange (ETDEWEB)

Taylor, Rebecca L. [School of Marine Science and Technology, University of Newcastle upon Tyne, Ridley Building, Claremont Road, Newcastle upon Tyne NE1 7RU (United Kingdom)]. E-mail: r.l.taylor@ncl.ac.uk; Caldwell, Gary S. [School of Marine Science and Technology, University of Newcastle upon Tyne, Ridley Building, Claremont Road, Newcastle upon Tyne NE1 7RU (United Kingdom); Bentley, Matthew G. [School of Marine Science and Technology, University of Newcastle upon Tyne, Ridley Building, Claremont Road, Newcastle upon Tyne NE1 7RU (United Kingdom)

2005-08-15

The recent discovery of the production of anti-proliferative aldehydes in a variety of microalgal species has lead to considerable investigation into the effects of these toxins on aquatic invertebrates. Studies have, however, rarely considered the impact pollutants may have on grazer responses to algal toxins. In this study, the acute toxicities of five aldehydes to the rotifer Brachionus plicatilis and nauplii of the brine shrimp Artemia salina are examined using immersion assays. In addition, the effect of a representative of these aldehydes in the presence of sub-lethal levels of heavy metals was examined. B. plicatilis generally showed greater sensitivity to the aldehydes than A. salina. The polyunsaturated 2-trans,4-trans-decadienal was the most toxic to both species having 24 h LD{sub 50} values of 7 and 20 {mu}M for B. plicatilis and A. salina, respectively. The remaining aldehydes had different orders of toxicity for the two species with a stronger relationship observed between mortality and aldehyde carbon-chain length for A. salina whereas B. plicatilis mortality showed a stronger dependence on the presence of carbon-carbon double bonds in the aldehydes. The presence of 1 {mu}M of copper sulphate in solutions of decadienal resulted in the reduction of the 24 h LD{sub 50} of decadienal by approximately a third for both species. 1 {mu}M of copper chloride in solutions of decadienal reduced the 24 h LD{sub 50} of decadienal to A. salina nauplii by approximately 11% and 1 {mu}M zinc sulphate caused a reduction of only 3%. Pre-exposure of the organisms to 1 {mu}M copper sulphate had no significant impact on their subsequent mortality in decadienal. The ecological implications and the possible mechanisms for the action of copper sulphate on the response of organisms to decadienal are discussed.

Toxicity of algal-derived aldehydes to two invertebrate species: Do heavy metal pollutants have a synergistic effect?

International Nuclear Information System (INIS)

Taylor, Rebecca L.; Caldwell, Gary S.; Bentley, Matthew G.

2005-01-01

The recent discovery of the production of anti-proliferative aldehydes in a variety of microalgal species has lead to considerable investigation into the effects of these toxins on aquatic invertebrates. Studies have, however, rarely considered the impact pollutants may have on grazer responses to algal toxins. In this study, the acute toxicities of five aldehydes to the rotifer Brachionus plicatilis and nauplii of the brine shrimp Artemia salina are examined using immersion assays. In addition, the effect of a representative of these aldehydes in the presence of sub-lethal levels of heavy metals was examined. B. plicatilis generally showed greater sensitivity to the aldehydes than A. salina. The polyunsaturated 2-trans,4-trans-decadienal was the most toxic to both species having 24 h LD 50 values of 7 and 20 μM for B. plicatilis and A. salina, respectively. The remaining aldehydes had different orders of toxicity for the two species with a stronger relationship observed between mortality and aldehyde carbon-chain length for A. salina whereas B. plicatilis mortality showed a stronger dependence on the presence of carbon-carbon double bonds in the aldehydes. The presence of 1 μM of copper sulphate in solutions of decadienal resulted in the reduction of the 24 h LD 50 of decadienal by approximately a third for both species. 1 μM of copper chloride in solutions of decadienal reduced the 24 h LD 50 of decadienal to A. salina nauplii by approximately 11% and 1 μM zinc sulphate caused a reduction of only 3%. Pre-exposure of the organisms to 1 μM copper sulphate had no significant impact on their subsequent mortality in decadienal. The ecological implications and the possible mechanisms for the action of copper sulphate on the response of organisms to decadienal are discussed

Are high rates of sulphate reduction associated with anaerobic oxidation of methane

Energy Technology Data Exchange (ETDEWEB)

Devol, A H; Ahmed, S I

1981-01-01

Classical models of sulphur diagenesis in marine sediments are based on the assumption that the rate of sulphate reduction is first order with respect to oxidizable particulate organic carbon (POC). This assumption requires that oxidizable POC, sulphate concentration and the sulphate reduction rate be highest at the top of the sulphate reduction zone and decrease exponentially with increasing sediment depth. However, to explain recent observations of concave upwards methane distributions, the anaerobic consumption of methane has been proposed. Furthermore, it has been proposed that this consumption takes place near the bottom of the sulphate reducing zone where sulphate concentrations are low. Thus, if sulphate reducing bacteria are associated with the anaerobic oxidation of methane, a peak in sulphate reduction rate might be expected in this deep consumption zone. The importance of the process in sedimentary sulphur diagenesis is indicated by calculations estimating that 30 to 75% of the downward sulphate flux at depth may be consumed by methane oxidation within this zone. We present here profiles of sulphate reduction rate in anoxic sediments that show distinct local maxima at the depth where the anaerobic oxidation of methane would be expected. Our measurements were made during July and August 1978 in Saanich Inlet, an anoxic fjord located on the south-east of Vancouver Island, British Columbia. The inlet has a shallow sill (approx 70 m) which restricts circulation of the deeper water (maximum depth 225 m) inside the basin to the extent that for about 8 months of the year the bottom waters contain hydrogen sulphide, the inlet is an ideal location for studying sedimentary sulphate reduction because reactions with oxygen and the effects of burrowing organisms can be neglected.

Bronchography in dogs. Comparative study with two barium sulphate solutions; Broncografía en perros. Estudio comparativo con dos concentraciones de sulfato de bario

Energy Technology Data Exchange (ETDEWEB)

Thibaut, J.; Gallardo, P.; Vargas, L.; Deppe, R.; Born, R. [Universidad Austral de Chile, Valdivia (Chile)

1998-07-01

Two solutions of barium sulphate, 60 and 30% w/v, were compared with the ''overflow'' Bronchographic method. Two groups of eight healthy adult does of both sexes, weighing 7 to 18 kg were used for the study. The dogs were anaesthetised with thiopentone sodium 2% (20 mg/kg iv). After intubation, each dog received contrast medium by a catheter connected to a syringe, in a 9 mi dose. Two series of two x-rays plates were taken in left lateral recumbent, 3 and 6 min after administering the contrast medium and in ventrodorsal projection, 30 sec. later. The x-ray plates obtained were analysed and compared intra and inter group considering the advance speed of the contrast medium, the radiographic density and outlines. Adverse reactions were controlled.

Reduction and aggregation of silver, copper and cadmium ions in aqueous solutions of gelatin and carboxymethyl cellulose

International Nuclear Information System (INIS)

Kapoor, S.; Gopinathan, C.

1998-01-01

Radiolytic reduction of silver, copper and cadmium ions and the subsequent formation of their clusters was studied in aqueous gelatin or carboxy methyl cellulose (CMC) solutions. Presence of gelatin or CMC in the solution affects the early processes. The rate of reduction by hydrated electron reduces due to complexation. However, when the ratio of silver ions to monomeric chains decreases over a certain limit the process of reduction inhibits completely. The effect of ionic strength or pH and the reducing radical on the rate of formation of colloidal Cu and Cd is also discussed

Microstructural aspects of manganese metal during its electrodeposition from sulphate solutions in the presence of quaternary amines

International Nuclear Information System (INIS)

Padhy, Subrat Kumar; Patnaik, P.; Tripathy, B.C.; Bhattacharya, I.N.

2015-01-01

Graphical abstract: - Highlights: • Quaternary amines produced smooth and bright manganese electrodeposits. • TEABr produced smooth and bright deposits with euhedral shaped crystals. • TBABr produced dendritic deposits with elongated poly-nodular crystals. • All the quaternary amines behaved as cathode polarisers. • TEABr was found to be the most efficient organic additive. - Abstract: In the present study investigation was made on the electrodeposition of manganese from sulphate solutions in the presence of quaternary amines TEABr, TPABr and TBABr. The concentrations of these additives were varied over a relatively broad range to evaluate their effect on the deposit morphology and preferred crystal orientations of the electrodeposited metal. TEABr resulted in bright and smooth manganese electrodeposits giving euhedral shape to the crystals with distinct triple junction points. TPABr also showed similar results at lower concentrations. However, TBABr resulted in the formation of dendritic growths with elongated poly-nodular crystals similar to that of Paragorgia corals having uniform multistep growths. The presence of these quaternary amines in the electrolyte causes polarisation of the cathode. TBABr being the strongest cathode polariser adsorbs strongly on the cathode resulting in poor deposit quality. TEABr was found to be the most efficient additive producing the desired quality manganese electrodeposit

Interaction of Celestine Concentrate and Reagent Grade SrSO4 with Oxalate Solutions

Directory of Open Access Journals (Sweden)

Abdullah Obut

2012-12-01

Full Text Available The interaction of reagent grade strontium sulphate and celestine concentrate with aqueous solutions of oxalic acid, sodiumoxalate and ammonium oxalate for the production of strontium carbonate were investigated for different oxalate compound:SrSO4 moleratios and reaction times using x-ray diffraction analysis and dissolution tests. Under the same experimental conditions, it was foundthat aqueous oxalic acid and sodium oxalate solutions had no or little effect on reagent grade strontium sulphate or celestineconcentrate, but aqueous ammonium oxalate solution converted them into strontium oxalate hydrate. Strontium carbonate was obtainedat conversion ratios of 74.7% for the celestine concentrate and 84.6 % for the reagent grade strontium sulphate by the decompositionof the obtained strontium oxalate hydrate at 600 °C under air atmosphere.

The investigation of deactivation the tailings from sulphate uranium technology

International Nuclear Information System (INIS)

Nikonov, V.I.; Knjazev, O.I.; Ruzin, L.I.; Smolnya, T.A.

2001-01-01

The purpose of investigation is to decrease contamination of the environment from wastes, produced on treatment of uranium ores by traditional sulphate uranium technology. In the result of treatment the sulphate uranium leaching cakes by 1-3 M chloride or nitrate of alkali-earth metals solutions, the content of radium decrease till (2.4 - 3.0) x 10 -8 Ci/kg. Produced deactivating solutions in which the content of radium-226 and other natural radionuclides exceeds of ten times the limit of tolerance safe concentrations for water (5.4 x 10 -11 Ci/l Ra-226) further may be treated by sorption or extraction. Due to the reason we pay our attention to the class of non-traditional ion-exchangers, which is the micellar wastes from production of antibiotics (MPW). The problems of it's utilization is very acute. MPW from antibiotics generates everyday is amount of tens tones (on dried mass), contents till 80% of moisture and include in solid phase 50 - 95 % organics in the work we used MPW from erythromycin in form of dried powder with size of particles to 0.05 - 0.16 mm. The possibility of radionuclides extraction by mixture of D2EHPA with TBP or TOPO for nitric deactivated solutions are investigated. It was received the complete extraction Th-230 into organic phase and next concentration with high content of isotope Th-230. Ra-D and Po are not recovered by the extractant. Using the extractant preliminary saturated with barium permit to extract completely Ra from solution. The method purification of technological solutions from activity with using solid extractants - TVEKS was developed. The TVEKS samples on styren-divinylbenzen copolymer base with size 1.0 - 1.5 mm were synthesized. The solid carrier was impregnated by D2EHPA or PN-1200 extractant solution in kerosene and used for extraction of radioactive elements (mainly Ra) from chloride acid solutions with summary activity 8.7 x 10 -10 Ci/l. TVEKS was activated by barium to capacity 1-3 mg/l for increasing purification

Computerised analysis of sulphate action on model concrete piles

Digital Repository Service at National Institute of Oceanography (India)

Deshmukh, A.M.; Balasubramanian, S.; Venugopal, C.

Sulphate action severely affects the durability of marine structures. It is imperative to study precisely the effects of magnesium sulphate on pile foundations in the marine environment. In the present paper an attempt is made to assess and analyse...

Ammonia leaching of copper smelter dust and precipitation as copper sulphide; Lixiviacion amoniacal de polvos de fundicion de cobre y precipitacion como sulfuro de cobre

Energy Technology Data Exchange (ETDEWEB)

Morales, A.; Hevia, J. F.; Cifuentes, G.

2009-07-01

The effect of ammonia on the leaching of copper smelter dust and copper precipitation from these solutions as sulphide using sulfur and sulfur dioxide was studied. The precipitation was done in ammoniacal media because this solution produced more satisfactory results at room temperature that a sulphuric media. A solid was precipitated containing 60 % of copper of the dust smelter. The other waste generated contained around 80 % of the arsenic of the original copper smelter dust. Based on the preliminary results obtained in this work it will propose a procedure for the recovery of copper as sulphide from copper smelter dust with parallel confinement of arsenic. (Author) 14 refs.

Ammonia, phosphate, phenol, and copper(II) removal from aqueous solution by subsurface and surface flow constructed wetland.

Science.gov (United States)

Mojiri, Amin; Ahmad, Zakiah; Tajuddin, Ramlah Mohd; Arshad, Mohd Fadzil; Gholami, Ali

2017-07-01

Water pollution is a global problem. During current study, ammonia, phosphate, phenol, and copper(II) were removed from aqueous solution by subsurface and surface flow constructed wetland. In current investigation, distilled water was polluted with four contaminants including ammonia, phosphate, copper (Cu), and phenol. Response surface methodology and central composite design were applied to optimize pollutant removal during treatment by subsurface flow constructed wetland (SSFCW). Contact time (12 to 80 h) and initial pollutant concentration (20 to 85 mg/L) were selected as independent factors; some upper and lower ranges were also monitored for accuracy. In SSFCW, water hyacinth transplanted in two substrate layers, namely zeolite and cockle shell. SSFCW removed 87.7, 81.4, 74.7, and 54.9% of ammonia, phosphate, Cu, and phenol, respectively, at optimum contact time (64.5 h) and initial pollutant concentration (69.2 mg/L). Aqueous solution was moved to a surface flow constructed wetland (SFCW) after treating via SSFCW at optimum conditions. In SFCW, Typha was transplanted to a fixed powdered substrate layer, including bentonite, zeolite, and cockle shell. SFCW could develop performance of this combined system and could improve elimination efficacy of the four contaminants to 99.99%. So this combined CW showed a good performance in removing pollutants. Graphical abstract Wetlands arrangement for treating aqueous solution in current study.

Bacterial sulphate reduction and the development of alkalinity. II. Laboratory experiments with soils

Energy Technology Data Exchange (ETDEWEB)

Abd-El-Malek, Y; Rizk, S G

1963-01-01

In waterlogged soils sulphate reduction was characterized by increases in counts of sulphate reducers, and increase in titratable alkalinity, insoluble carbonate, and soluble sulphides, and a decrease in soluble Ca/sup 2 +/ + Mg/sup 2 +/. Presence of organic matter greatly enhanced sulphate reduction. A linear relationship between the amount of sulphate reduced and increases in titratable alkalinity and insoluble carbonate were apparent. The potential effects of sulphate reduction on soil fertility through the development of alkalinity are discussed.

Safety and efficacy of Bolus administration of magnesium sulphate ...

African Journals Online (AJOL)

Safety and efficacy of Bolus administration of magnesium sulphate for preeclampsia. ... On-going research is addressing its administration in terms of dosage, duration and safety. Objective: We evaluated a ... Keywords: safety, efficacy, bolus magnesium sulphate, preeclampsia, University of Benin Teaching Hospital

Is Copper Immune to Corrosion When in Contact With Water and Aqueous Solutions?

International Nuclear Information System (INIS)

Macdonald, Digby D.; Sharifi-Asl, Samin

2011-03-01

Objectives The aim of this project has been to increase knowledge and to contribute to the research community in the area of copper corrosion in a repository environment. For SSM, the most important subject is to provide better conditions for a science based evaluation of a repository for spent nuclear fuel. In this respect, this project aimed at conducting a comprehensive theoretical study on corrosion of copper in repository environment based on an expected composition of dissolved species in the groundwater in the Forsmark area. In addition the thermodynamic immunity of copper in pure anoxic water has been especially addressed as this was one of the initial conditions made by SKB for selecting copper as canister material. Results The authors have shown, in so-called corrosion Domain Diagrams, that copper in a thermodynamic sense can be considered as immune in pure anoxic water (without dissolved oxygen) only under certain conditions. It is shown that copper will corrode in pure anoxic water with very low concentrations of [Cu + ] and very low partial pressures of hydrogen gas. At higher concentrations of [Cu + ] and partial pressures of hydrogen, copper is found to be thermodynamically immune and will not corrode. The rate of copper corrosion in the repository water environment will thus depend on the transport of corrosion products away from the copper surface or the transport of corroding species to the copper surface. The degree to which this affects the corrosion of copper canisters in the repository environment has not been further studied. Still, the result shows that copper cannot be considered as thermodynamically immune in the presence of pure anoxic water, this implicate that one of SKB:s initial conditions for selecting copper as a canister material can be questioned. To what degree this may influence the corrosion of copper canisters in the repository environment still needs to be investigated. Of other species present in the water at repository

Is Copper Immune to Corrosion When in Contact With Water and Aqueous Solutions?

Energy Technology Data Exchange (ETDEWEB)

Macdonald, Digby D.; Sharifi-Asl, Samin (Pennsylvania State Univ., PA (United States). Center for Electrochemical Science and Technology, Dept. of Materials Science and Engineering)

2011-03-15

Objectives The aim of this project has been to increase knowledge and to contribute to the research community in the area of copper corrosion in a repository environment. For SSM, the most important subject is to provide better conditions for a science based evaluation of a repository for spent nuclear fuel. In this respect, this project aimed at conducting a comprehensive theoretical study on corrosion of copper in repository environment based on an expected composition of dissolved species in the groundwater in the Forsmark area. In addition the thermodynamic immunity of copper in pure anoxic water has been especially addressed as this was one of the initial conditions made by SKB for selecting copper as canister material. Results The authors have shown, in so-called corrosion Domain Diagrams, that copper in a thermodynamic sense can be considered as immune in pure anoxic water (without dissolved oxygen) only under certain conditions. It is shown that copper will corrode in pure anoxic water with very low concentrations of [Cu+] and very low partial pressures of hydrogen gas. At higher concentrations of [Cu+] and partial pressures of hydrogen, copper is found to be thermodynamically immune and will not corrode. The rate of copper corrosion in the repository water environment will thus depend on the transport of corrosion products away from the copper surface or the transport of corroding species to the copper surface. The degree to which this affects the corrosion of copper canisters in the repository environment has not been further studied. Still, the result shows that copper cannot be considered as thermodynamically immune in the presence of pure anoxic water, this implicate that one of SKB:s initial conditions for selecting copper as a canister material can be questioned. To what degree this may influence the corrosion of copper canisters in the repository environment still needs to be investigated. Of other species present in the water at repository depth in

Removal of copper (II from aqueous solutions by adsorption onto granular activated carbon in the presence of competitor ions

Directory of Open Access Journals (Sweden)

Saeed Almohammadi

2016-04-01

Full Text Available In this work, the removal of copper from an aqueous solution by granular activated carbon (GAC in the presence of competitor ions was studied. A batch adsorption was carried out and different parameters such as pH, contact time, initial copper concentration and competitor ions concentration were changed to determine the optimum conditions for adsorption. The optimum pH required for maximum adsorption was found to be 4.5 for copper. Equilibrium was evaluated at 144 h at room temperature. The removal efficiency of Cu(II was 71.12% at this time. The kinetics of copper adsorption on activated carbon followed the pseudo second-order model. The experimental equilibrium sorption data were tested using the Langmuir, Freundlich, Temkin and Dubinin–Radushkevich (D-R equations and the Langmuir model was found to be well fitted for copper adsorption onto GAC. The maximum adsorption capacity of the adsorbent for Cu(II was calculated from the Langmuir isotherm and found to be 7.03 mg/g. Subsequently, the removal of copper by granular activated carbon in the presence of Ag1+ and Mn2+ as competitor ions was investigated. The removal efficiency of Cu(II ions without the presence of the competitor ions was 46% at 6 h, while the removal efficiency of Cu(II ions in the presence of competitor ions, Ag1+ and Mn2+ , was 34.76% and 31.73%, respectively.

Unintended consequences of atmospheric injection of sulphate aerosols.

Energy Technology Data Exchange (ETDEWEB)

Brady, Patrick Vane; Kobos, Peter Holmes; Goldstein, Barry

2010-10-01

Most climate scientists believe that climate geoengineering is best considered as a potential complement to the mitigation of CO{sub 2} emissions, rather than as an alternative to it. Strong mitigation could achieve the equivalent of up to -4Wm{sup -2} radiative forcing on the century timescale, relative to a worst case scenario for rising CO{sub 2}. However, to tackle the remaining 3Wm{sup -2}, which are likely even in a best case scenario of strongly mitigated CO{sub 2} releases, a number of geoengineering options show promise. Injecting stratospheric aerosols is one of the least expensive and, potentially, most effective approaches and for that reason an examination of the possible unintended consequences of the implementation of atmospheric injections of sulphate aerosols was made. Chief among these are: reductions in rainfall, slowing of atmospheric ozone rebound, and differential changes in weather patterns. At the same time, there will be an increase in plant productivity. Lastly, because atmospheric sulphate injection would not mitigate ocean acidification, another side effect of fossil fuel burning, it would provide only a partial solution. Future research should aim at ameliorating the possible negative unintended consequences of atmospheric injections of sulphate injection. This might include modeling the optimum rate and particle type and size of aerosol injection, as well as the latitudinal, longitudinal and altitude of injection sites, to balance radiative forcing to decrease negative regional impacts. Similarly, future research might include modeling the optimum rate of decrease and location of injection sites to be closed to reduce or slow rapid warming upon aerosol injection cessation. A fruitful area for future research might be system modeling to enhance the possible positive increases in agricultural productivity. All such modeling must be supported by data collection and laboratory and field testing to enable iterative modeling to increase the

Incorporation of copper ions into crystals of T2 copper-depleted laccase from Botrytis aclada

International Nuclear Information System (INIS)

Osipov, E. M.; Polyakov, K. M.; Tikhonova, T. V.; Kittl, R.; Dorovatovskii, P.V.; Shleev, S. V.; Popov, V. O.; Ludwig, R.

2015-01-01

The restoration of the native form of laccase from B. aclada from the type 2 copper-depleted form of the enzyme was investigated. Copper ions were found to be incorporated into the active site after soaking the depleted enzyme in a Cu + -containing solution. Laccases belong to the class of multicopper oxidases catalyzing the oxidation of phenols accompanied by the reduction of molecular oxygen to water without the formation of hydrogen peroxide. The activity of laccases depends on the number of Cu atoms per enzyme molecule. The structure of type 2 copper-depleted laccase from Botrytis aclada has been solved previously. With the aim of obtaining the structure of the native form of the enzyme, crystals of the depleted laccase were soaked in Cu + - and Cu 2+ -containing solutions. Copper ions were found to be incorporated into the active site only when Cu + was used. A comparative analysis of the native and depleted forms of the enzymes was performed

Bacterial sulphate reduction and the development of alkalinity. I. Experiments with synthetic media

Energy Technology Data Exchange (ETDEWEB)

Abd-El-Malek, Y; Rizk, S G

1963-01-01

In liquid cultures of desulphovibrio desulphuricans the effects of the following on sulphate reduction were determined: The type of cation (ca++ or na+) attached to the sulphate ion; the presence of calcium carbonate alone and with sodium chloride; the concentration of sodium sulphate, sodium lactate and sodium chloride; and the initial pH. The titratable alkalinity formed as a result of sulphate reduction was found to be quantitatively related to the sulphate reduced, and apparently unaffected by strain variation or energy source.

Sulphation reactions of oxidic dust particles in waste heat boiler environment. Literature review

Energy Technology Data Exchange (ETDEWEB)

Ranki, T.

1999-09-01

Sulphation of metal oxides has an important role in many industrial processes. In different applications sulphation reactions have different aims and characteristics. In the flash smelting process sulphation of oxidic flue dust is a spontaneous and inevitable phenomena, which takes place in the waste heat boiler (WHB) when cooling down hot dust laden off-gases from sulphide smelters. Oxidic dust particles (size 0 - 50 {mu}m) react with O{sub 2} and SO{sub 2} or SO{sub 3} in a certain temperature range (500 - 800 deg C). Sulphation reactions are highly exothermic releasing large amount of heat, which affects the gas cooling and thermal performance of the boiler. Thermodynamics and kinetics of the system have to be known to improve the process and WHB operation. The rate of sulphation is affected by the prevailing conditions (temperature, gas composition) and particle size and microstructure (porosity, surface area). Some metal oxides (CuO) can react readily with SO{sub 2} and O{sub 2} and act as self-catalysts, but others (NiO) require the presence of an external catalyst to enhance the SO{sub 3} formation and sulphation to proceed. Some oxides (NiO) sulphate directly, some (CuO) may form first intermediate phases (basic sulphates) depending on the reaction conditions. Thus, the reaction mechanisms are very complex. The aim of this report was to search information about the factors affecting the dust sulphation reactions and suggested reaction mechanisms and kinetics. Many investigators have studied sulphation thermodynamics and reaction kinetics and mechanisms of macroscopical metal oxide pieces, but only few articles have been published about sulphation of microscopical particles, like dust. All the found microscale studies dealt with sulphation reactions of calcium oxide, which is not present in the flash smelting process, but used as an SO{sub 2} absorbent in the combustion processes. However, also these investigations may give some hints about the sulphation

Interaction of aconitine with bovine serum albumin and effect of atropine sulphate and glycyrrhizic acid on the binding

International Nuclear Information System (INIS)

Huang Yun; Cui Lijian; Wang Jianming; Huo Kun; Chen Chen; Zhan Wenhong; Wang Yongli

2012-01-01

The interaction of aconitine with bovine serum albumin (BSA) and effect of atropine sulphate and glycyrrhizic acid on binding constant, binding sites, and conformation were studied in an aqueous buffer solution (pH 7.40) by ultraviolet absorption and fluorescence spectroscopy. The study results show that aconitine quenched the endogenous fluorescence of BSA via a dynamic quenching procedure. Predominant intermolecular forces between aconitine and BSA were hydrophobic interactions, which stabilized the complex of aconitine–BSA. The distance between the donor and acceptor was 2.62 nm. The conformation of BSA was investigated by synchronous fluorescence techniques, indicating that the microenvironment around tryptophan (Trp) residues was changed. Furthermore, with the addition of atropine sulphate or glycyrrhizic acid, binding constant and the number of binding sites of aconitine to BSA were decreased, and the conformation had no change, which provide an important theoretical support for aconitine detoxification by atropine sulphate and glycyrrhizic acid. - Highlights: ► Effect of atropine or glycyrrhizic acid on aconitine–BSA binding. ► UV–vis absorption and fluorescence spectroscopic techniques used. ► Aconitine quenched BSA fluorescence via dynamic quenching with r=2.62 nm. ► Atropine sulphate and glycyrrhizic acid decreased K A and n of aconitine–BSA. ► Support for aconitine detoxification by atropine and glycyrrhizic acid.

Thermal decomposition of uranyl sulphate hydrate

International Nuclear Information System (INIS)

Sato, T.; Ozawa, F.; Ikoma, S.

1980-01-01

The thermal decomposition of uranyl sulphate hydrate (UO 2 SO 4 .3H 2 O) has been investigated by thermogravimetry, differential thermal analysis, X-ray diffraction and infrared spectrophotometry. As a result, it is concluded that uranyl sulphate hydrate decomposes thermally: UO 2 SO 4 .3H 2 O → UO 2 SO 4 .xH 2 O(2.5 = 2 SO 4 . 2H 2 O → UO 2 SO 4 .H 2 O → UO 2 SO 4 → α-UO 2 SO 4 → β-UO 2 SO 4 → U 3 O 8 . (author)

Magnesium sulphate for fetal neuroprotection

DEFF Research Database (Denmark)

Bickford, Celeste D; Magee, Laura A; Mitton, Craig

2013-01-01

of cerebral palsy (CP) averted and quality-adjusted life years (QALYs). RESULTS: From a health system and a societal perspective, respectively, a savings of $2,242 and $112,602 is obtained for each QALY gained and a savings of $30,942 and $1,554,198 is obtained for each case of CP averted when magnesium......BACKGROUND: The aim of this study was to assess the cost-effectiveness of administering magnesium sulphate to patients in whom preterm birth at ... sensitivity analyses were used to compare the administration of magnesium sulphate with the alternative of no treatment. Two separate cost perspectives were utilized in this series of analyses: a health system and a societal perspective. In addition, two separate measures of effectiveness were utilized: cases...

Relationship between sulphate and sulphur dioxide in the air

Energy Technology Data Exchange (ETDEWEB)

Fugas, M; Gentilizza, M

1978-01-01

The relationship between the sulphate in suspended particulates and sulphur dioxide in the air was studied in various urban and industrial areas. The relationship is best described by the equation y = ax/sup b/, where y is the percentage of the sulphate S in the total S (sulphate and sulphur dioxide) and x is the concentration of the total S in the air. The regression coefficients a and b seem to be characteristics of the area. In urban areas studied so far a was between 316 and 378 and b between -0.74 and -0.83. In industrial areas polluted by dust which contains elevated concentrations of metals a was between 91 and 107 and b between -0.35 and -0.49. In the area polluted by cement dust there was practically no correlation between the sulphate S (%) and the total S, but a relatively high correlation between absolute amounts of the sulphate S and the total S. The relations indicate that the limitation of SO/sub 2/ conversion is influenced by aerosol composition. Aerosols containing certain metals may promote the conversion by a catalytic effect while alkaline substances by increasing the pH. Whether this can only happen in the plume or in the air as well remains to be clarified.

Adsorption of Copper Ion using Acrylic Acid-g-Polyaniline in Aqueous Solution

Science.gov (United States)

Kamarudin, Sabariah; Mohammad, Masita

2018-04-01

A conductive polymer, polyaniline (PANI) has unique electrical behaviour, stable in the environment, easy synthesis and have wide application in various fields. Modification of PANI in order to improve its adsorption capacity has been done. In this study, the polyaniline-grafted acrylic acid has been prepared and followed by adsorption of copper ion in aqueous solution. Acrylic acid, PANI and acrylic acid-g-polyaniline (Aag-PANI) were characterized by FTIR and SEM to determine its characteristic. The adsorption capacity was investigated to study the removal capacity of Cu ion from aqueous solution. Two parameters were selected which are pH (2, 4 and 6) and initial metal ion concentration (50 mg/L, 100 mg/L and 200 mg/L). The maximum adsorption capacity for PANI and Aag-PANI are 1.7 mg/g and 64.6 mg/g, respectively, at an initial concentration of 100 mg/L. The Langmuir adsorption isotherm model and Freundlich adsorption isotherm model have been used and showed that it is heterolayer adsorption by follows the Freundlich isotherm model.

Photoelectrochemistry of copper(I) acetylide films electrodeposited onto copper electrodes

Energy Technology Data Exchange (ETDEWEB)

Zotti, G.; Cattarin, S.; Mengoli, G.; Fleischmann, M.; Peter, L.M.

1986-01-01

Films of copper acetylide (Cu/sub 2/C/sub 2/) were grown electrochemically on copper and characterized by transmittance and reflectance techniques. The photoelectrochemical properties of the filmed electrodes in alkaline solution indicate that Cu/sub 2/C/sub 2/ behaves as a p-type semiconducting material (1.5 eV band gap). The photocurrents depend on film thickness and aging and high resistivity or recombination losses limit the quantum yield to some 4% for thicknesses of practical importance (250 nm).

Copper accumulation by stickleback nests containing spiggin.

Science.gov (United States)

Pinho, G L L; Martins, C M G; Barber, I

2016-07-01

The three-spined stickleback is a ubiquitous fish of marine, brackish and freshwater ecosystems across the Northern hemisphere that presents intermediate sensitivity to copper. Male sticklebacks display a range of elaborate reproductive behaviours that include nest construction. To build the nests, each male binds nesting material together using an endogenous glycoprotein nesting glue, known as 'spiggin'. Spiggin is a cysteine-rich protein and, therefore, potentially binds heavy metals present in the environment. The aim of this study was to investigate the capacity of stickleback nests to accumulate copper from environmental sources. Newly built nests, constructed by male fish from polyester threads in laboratory aquaria, were immersed in copper solutions ranging in concentration from 21.1-626.6 μg Cu L(-1). Bundles of polyester threads from aquaria without male fish were also immersed in the same copper solutions. After immersion, nests presented higher amounts of copper than the thread bundles, indicating a higher capacity of nests to bind this metal. A significant, positive correlation between the concentration of copper in the exposure solution and in the exposed nests was identified, but there was no such relationship for thread bundles. Since both spiggin synthesis and male courtship behaviour are under the control of circulating androgens, we predicted that males with high courtship scores would produce and secrete high levels of the spiggin protein. In the present study, nests built by high courtship score males accumulated more copper than those built by low courtship score males. Considering the potential of spiggin to bind metals, the positive relationship between fish courtship and spiggin secretion seems to explain the higher amount of copper on the nests from the fish showing high behaviour scores. Further work is now needed to determine the consequences of the copper binding potential of spiggin in stickleback nests for the health and survival of

Core Sulphate-Reducing Microorganisms in Metal-Removing Semi-Passive Biochemical Reactors and the Co-Occurrence of Methanogens

Directory of Open Access Journals (Sweden)

Maryam Rezadehbashi

2018-02-01

Full Text Available Biochemical reactors (BCRs based on the stimulation of sulphate-reducing microorganisms (SRM are emerging semi-passive remediation technologies for treatment of mine-influenced water. Their successful removal of metals and sulphate has been proven at the pilot-scale, but little is known about the types of SRM that grow in these systems and whether they are diverse or restricted to particular phylogenetic or taxonomic groups. A phylogenetic study of four established pilot-scale BCRs on three different mine sites compared the diversity of SRM growing in them. The mine sites were geographically distant from each other, nevertheless the BCRs selected for similar SRM types. Clostridia SRM related to Desulfosporosinus spp. known to be tolerant to high concentrations of copper were members of the core microbial community. Members of the SRM family Desulfobacteraceae were dominant, particularly those related to Desulfatirhabdium butyrativorans. Methanogens were dominant archaea and possibly were present at higher relative abundances than SRM in some BCRs. Both hydrogenotrophic and acetoclastic types were present. There were no strong negative or positive co-occurrence correlations of methanogen and SRM taxa. Knowing which SRM inhabit successfully operating BCRs allows practitioners to target these phylogenetic groups when selecting inoculum for future operations.

Cyanide and Copper Recovery from Barren Solution of the Merrill Crowe Process

Science.gov (United States)

Parga, José R.; Valenzuela, Jesús L.; Díaz, J. A.

This paper is a brief overview of the role of inducing the nucleated precipitation of copper and cyanide in a flashtube serpentine reactor, using sodium sulfide as the precipitate and sulfuric acid as pH control. The results showed that pH had a great effect on copper cyanide removal efficiency and the optimum pH was about 3 to 3.5. At this pH value copper cyanide removal efficiency could be achieved above 97 and 99 %, when influent copper concentration ions were 650 and 900 ppm respectively. In this process the cyanide associated with the copper, zinc, iron cyanide complexes are released as HCN gas under strong acidic conditions, allowing it to be recycled back to the cyanidation process as free cyanide.

Feasibility of lead removal from industrial effluents by sulphate reducing bacteria

International Nuclear Information System (INIS)

Nunez, L. A.; Diez, M.; Rodriguez, F. J.

2009-01-01

Battery manufacturing wastewater contains high concentration of sulphate and lead at low pH values. Biogical treatment by anaerobic reduction of sulphate to sulphite, with organic matter as electron donor, increases alkalinity and allow precipitating lead as sulphide. the type of organic matter, COD/SO 4 ratio and lead concentration over sulphate reduction rate are investigated in this work. (Author)

Differential responses of freshwater wetland soils to sulphate pollution

NARCIS (Netherlands)

Lamers, L.P.M.; Dolle, ten G.E.; Berg, van den S.T.G.; Delft, van S.P.J.; Roelofs, J.G.M.

2001-01-01

Sulphate (SO42-) reduction rates are generally low in freshwater wetlands and are regulated by the scarce availability of the ion. Increased concentrations of this electron acceptor due to sulphur (S) pollution of groundwater and surface water may, however, lead to high sulphate reduction rates now

The effect of magnesium on partial sulphate removal from mine water as gypsum.

Science.gov (United States)

Tolonen, Emma-Tuulia; Rämö, Jaakko; Lassi, Ulla

2015-08-15

The aim of this research was to investigate the effect of magnesium on the removal efficiency of sulphate as gypsum from mine water. The precipitation conditions were simulated with MINEQL + software and the simulation results were compared with the results from laboratory jar test experiments. Both the simulation and the laboratory results showed that magnesium in the mine water was maintaining sulphate in a soluble form as magnesium sulphate (MgSO4) at pH 9.6. Thus magnesium was preventing the removal of sulphate as gypsum (CaSO4·2H2O). However, change in the lime precipitation pH from 9.6 to 12.5 resulted in magnesium hydroxide (Mg(OH)2) precipitation and improved sulphate removal. Additionally, magnesium hydroxide could act as seed crystals for gypsum precipitation or co-precipitate sulphate further enhancing the removal of sulphate from mine water. Copyright © 2015 Elsevier Ltd. All rights reserved.

Sulphated glycosaminoglycans and proteoglycans in the developing vertebral column of juvenile Atlantic salmon (Salmo salar)

OpenAIRE

Hannesson, Kirsten O.; Ytteborg, Elisabeth; Takle, Harald; Enersen, Grethe; B?verfjord, Grete; Pedersen, Mona E.

2015-01-01

In the present study, the distribution of sulphated glycosaminoglycans (GAGs) in the developing vertebral column of Atlantic salmon (Salmo salar) at 700, 900, 1100 and 1400?d? was examined by light microscopy. The mineralization pattern was outlined by Alizarin red S and soft structures by Alcian blue. The temporal and spatial distribution patterns of different types of GAGs: chondroitin-4-sulphate/dermatan sulphate, chondroitin-6-sulphate, chondroitin-0-sulphate and keratan sulphate were add...

Visual Observation of Dissolution of Copper Ions from a Copper Electrode

Science.gov (United States)

Ikemoto, Isao; Saitou, Kouichi

2013-01-01

During electrolysis, to visually observe the conversion of a metal to its cation, either the cation or its complex ion should have a distinct color while the electrolyte solution must be colorless and transparent. A demonstration is described in which copper is used as the electrodes and sodium polyacrylate (a superabsorbent polymer) solution is…

Study on Selective Removal of Impurity Iron from Leached Copper-Bearing Solution Using a Chelating Resin

Directory of Open Access Journals (Sweden)

Yubiao Li

2016-10-01

Full Text Available In order to selectively remove iron from copper laden solution after leaching but prior to electrowinning, equilibrium, kinetic, and thermodynamic studies have been conducted on an a chelating resin of Rexp-501 at pH 1.0 and at various temperatures. Both Langmuir and Freundlich models were investigated, with the Langmuir model proving to be more suitable for fitting iron removal performance, with little influence from copper concentration. Compared with the pseudo first order kinetic model, the pseudo second order kinetic model fitted the dynamic adsorption process better, indicating a chemisorption mechanism. Fourier transform infrared spectroscopy (FT-IR results indicated that C=O from carbonyl group played a key role in combining with iron and can be regenerated and reused. However, the C=O of the acylamino group combining with iron was not able to be released after oxalic acid was applied.

Microwave assisted synthesis of nano sized sulphate doped hydroxyapatite

International Nuclear Information System (INIS)

Alshemary, Ammar Z.; Goh, Yi-Fan; Akram, Muhammad; Razali, Ili Rabihah; Abdul Kadir, Mohammed Rafiq; Hussain, Rafaqat

2013-01-01

Highlights: ► Phase pure nano-sized sulphur doped hydroxyapatite has been synthesized. ► TEM analysis confirmed formation of needle shaped structure. ► Lattice parameters and cell volume increased with increase in sulphate doping. ► Crystallite size decreased as sulphate content inside the structure increased. ► Degree of crystallinity decreased with increase in sulphate substitution. - Abstract: Inorganic sulphate is required by all mammalian cells to function properly, it is the fourth most abundant anion in the human plasma. Sulphate ions are the major source of sulphur which is considered an important element for sustenance of life as it is present in the essential amino and is required by cells to function properly. In this study we have successfully substituted sulphate ions (SO 4 2− ) into hydroxyapatite (Ca 10 (PO 4 ) 6−x (SO 4 ) x (OH) 2−x ) lattice via ion exchange process with phosphate group. Concentration of SO 4 2− ions was varied between X = 0.05–0.5, using (Ca (NO 3 ) 2 ·4H 2 O), ((NH 4 ) 2 HPO 4 ) and (Na 2 SO 4 ) as starting materials. X-ray diffraction (XRD), Fourier transform IR spectroscopy (FTIR), showed that the substitution of SO 4 2− ions into the lattice resulted in peak broadening and reduced peak height due to the amorphous nature and reduced crystallinity of the resulting HA powder. Transmission electron microscopy (TEM) and field emission electron microscopy (FESEM) analysis confirmed the formation of needle shaped particles of 41 nm size with homogenous and uniform distribution of element within the HA structure

Electrochemical behaviour of alkaline copper complexes

Indian Academy of Sciences (India)

Abstract. A search for non-cyanide plating baths for copper resulted in the development of alkaline copper complex baths containing trisodium citrate [TSC] and triethanolamine [TEA]. Voltammetric studies were carried out on platinum to understand the electrochemical behaviour of these complexes. In TSC solutions, the.

Biosorption of copper (II) from aqueous solution by mycelial pellets ...

African Journals Online (AJOL)

The optimum diameter and pH for biosorption of copper (II) was found to be 1.0 to 1.2 mm and 4.0. Evaluation of the experimental data in terms of biosorption dynamics showed that the biosorption of copper (II) onto MPRO followed the pseudo-second-order kinetic model. The equilibrium data fitted very well to the Langmuir ...

Serum and urinary oestrone sulphate in pregnancy and delivery measured by a direct radioimmunoassay

International Nuclear Information System (INIS)

Honjo, Hideo; Kitawaki, Jo; Itoh, Masafumi; Yasuda, Jinsuke; Yamamoto, Takara; Yamamoto, Takao; Okada, Hiroji; Ohkubo, Tadashi; Nambara, Toshio

1986-01-01

Serum and urinary levels of oestrone sulphate in pregnancy and delivery were measured by a direct radioimmunoassay without hydrolysis. the serum and urinary oestrone sulphate increased as pregnancy progressed. the mean level of serum oestrone sulphate increased to the highest peak of 494 pmol/ml at the 35th gestational week and then decreased. The mean level of urinary oestrone sulphate increased to the highest peak of 1.28 μmol/l at the 34th gestational week and the decreased. At vaginal deliveries, the mean level of maternal peripheral serum oestrone sulphate increased hourly at as high a level as 979 pmol/ml. The mean serum level of oestrone sulphate was 204 pmol/ml in the umbilical artery and 145 pmol/ml in the umbilical vein. At Caesarean section, on the other hand, the maternal peripheral serum level of oestrone sulphate averaged 362 pmol/ml. The mean serum levels of oestrone sulphate wre 90.7 pmol/ml and 171 pmol/ml in the umbilical artery and umbilical vein, respectively. These results suggest a maternal origin of oestrone sulphate in pregnancy, with fluctuations in the levels being of interest in relation to labour pain. (author)

Analysis of the hygroscopic and volatile properties of ammonium sulphate seeded and unseeded SOA particles

Science.gov (United States)

Meyer, N. K.; Duplissy, J.; Gysel, M.; Metzger, A.; Dommen, J.; Weingartner, E.; Alfarra, M. R.; Prevot, A. S. H.; Fletcher, C.; Good, N.; McFiggans, G.; Jonsson, Â. M.; Hallquist, M.; Baltensperger, U.; Ristovski, Z. D.

2009-01-01

The volatile and hygroscopic properties of ammonium sulphate seeded and unseeded secondary organic aerosol (SOA) derived from the photo-oxidation of atmospherically relevant concentrations of α-pinene were studied. The seed particles were electrospray generated ammonium sulphate ((NH4)2SO4) having diameters of approximately 33 nm with a quasi-mono-disperse size distribution (geometric standard deviation σg=1.3). The volatile and hygroscopic properties of both seeded and unseeded SOA were simultaneously measured with a VH-TDMA (volatility - hygroscopicity tandem differential mobility analyzer). VH-TDMA measurements of unseeded SOA show a decrease in the hygroscopic growth (HGF) factor for increased volatilisation temperatures such that the more volatile compounds appear to be more hygroscopic. This is opposite to the expected preferential evaporation of more volatile but less hygroscopic material, but could also be due to enhanced oligomerisation occurring at the higher temperature in the thermodenuder. In addition, HGF measurements of seeded SOA were measured as a function of time at two relative humidities, below (RH 75%) and above (RH 85%) the deliquescence relative humidity (DRH) of the pure ammonium sulphate seeds. As these measurements were conducted during the onset phase of photo-oxidation, during particle growth, they enabled us to find the dependence of the HGF as a function of the volume fraction of the SOA coating. HGF's measured at RH of 85% showed a continuous decrease as the SOA coating thickness increased. The measured growth factors show good agreements with ZSR predictions indicating that, at these RH values, there are only minor solute-solute interactions. At 75% RH, as the SOA fraction increased, a rapid increase in the HGF was observed indicating that an increasing fraction of the (NH4)2SO4 is subject to a phase transition, going into solution, with an increasing volume fraction of SOA. To our knowledge this is the first time that SOA derived

Leaching for recovery of copper from municipal solid waste incineration fly ash: influence of ash properties and metal speciation.

Science.gov (United States)

Lassesson, Henric; Fedje, Karin Karlfeldt; Steenari, Britt-Marie

2014-08-01

Recovery of metals occurring in significant amounts in municipal solid waste incineration fly ash, such as copper, could offer several advantages: a decreased amount of potentially mobile metal compounds going to landfill, saving of natural resources and a monetary value. A combination of leaching and solvent extraction may constitute a feasible recovery path for metals from municipal solid waste incineration fly ash. However, it has been shown that the initial dissolution and leaching is a limiting step in such a recovery process. The work described in this article was focused on elucidating physical and chemical differences between two ash samples with the aim of explaining the differences in copper release from these samples in two leaching methods. The results showed that the chemical speciation is an important factor affecting the release of copper. The occurrence of copper as phosphate or silicate will hinder leaching, while sulphate and chloride will facilitate leaching. © The Author(s) 2014.

Influence of sulphate ions on the composition and structure of the oxide films on stainless steel and nickel alloys in simulated BWR crack conditions

International Nuclear Information System (INIS)

Bojinov, M.; Kinnunen, P.; Laitinen, E.; Maekelae, K.; Saario, T.; Sirkiae, P.; Toivonen, A.; Campbell, J.M.; Johansson, L.S.; Helin, M.; Muttilainen, E.; Reinvall, A.; Ollonqvist, T.; Vaeyrynen, J.

2002-01-01

The goal of the present work has been to clarify the influence of sulphate ions on the oxide films formed on stainless steel and Ni-based alloys in simulated crack chemistry conditions using different ex situ analytical techniques. The main observations of this work can be summarised as follows: The thickness of the films formed in simulated oxygen-free crack chemistry conditions during an exposure of circa 4 days varies roughly in the range 200..500 nm, which corresponds to observations reported in the literature [2]. The presence of 10000 ppb sulphate ions in simulated crack tip conditions seems to lead to a considerably lower thickness of the oxide films when compared to sulphate-free conditions. The presence of 10000 ppb sulphate ions leads also to considerable changes in the morphology of the oxide crystals on the material samples. In the absence of sulphate the outer oxide layer contains elongated round-edged crystals, while in the presence of sulphate ions the crystals are longish and needle-like. No visible difference can be observed in the outlook of the crystals formed on stainless steel and Inconel alloy surfaces. A small amount of sulphur in the form of sulphate can be found on the oxide surface on all the studied materials after exposure to the 10000 ppb solution. Sulphur seems to become incorporated inside the oxide film on AISI 316 L(NG). It is not clear at this stage, whether the observed influence of the sulphate ions can be ascribed to the lower pH, to a possible effect on solubility or to a direct influence of the anionic species. (authors)

The hypobranchial mucin of the whelk Buccinum undatum L. The polysaccharide sulphate component.

Science.gov (United States)

Hunt, S; Jevons, F R

1966-02-01

1. A polysaccharide sulphate has been isolated from the hypobranchial mucin of the whelk Buccinum undatum. 2. The molecular weight of this polysaccharide, which is a glucan carrying one ester sulphate group per monosaccharide residue, is 1.7x10(5). 3. Some investigations bearing on the location of the ester sulphate groups are reported. 4. The viscosity of the whole mucin has been shown to depend mainly on the glucan sulphate.

Microwave assisted synthesis of nano sized sulphate doped hydroxyapatite

Energy Technology Data Exchange (ETDEWEB)

Alshemary, Ammar Z.; Goh, Yi-Fan; Akram, Muhammad; Razali, Ili Rabihah [Department of Chemistry, Faculty of Science, Universiti Teknologi Malaysia, 81310 UTM Skudai, Johor Darul Ta’zim (Malaysia); Abdul Kadir, Mohammed Rafiq [Medical Implant Technology Group, Faculty of Biomedical Engineering and Health Science, Universiti Teknologi Malaysia,81310 UTM Skudai, Johor Darul Ta’zim (Malaysia); Hussain, Rafaqat, E-mail: rafaqat@kimia.fs.utm.my [Ibnu Sina Institute for Fundamental Science Studies, Universiti Teknologi Malaysia, 81310 UTM Skudai, Johor DarulTa’zim (Malaysia)

2013-06-01

Highlights: ► Phase pure nano-sized sulphur doped hydroxyapatite has been synthesized. ► TEM analysis confirmed formation of needle shaped structure. ► Lattice parameters and cell volume increased with increase in sulphate doping. ► Crystallite size decreased as sulphate content inside the structure increased. ► Degree of crystallinity decreased with increase in sulphate substitution. - Abstract: Inorganic sulphate is required by all mammalian cells to function properly, it is the fourth most abundant anion in the human plasma. Sulphate ions are the major source of sulphur which is considered an important element for sustenance of life as it is present in the essential amino and is required by cells to function properly. In this study we have successfully substituted sulphate ions (SO{sub 4}{sup 2−}) into hydroxyapatite (Ca{sub 10}(PO{sub 4}){sub 6−x}(SO{sub 4}){sub x}(OH){sub 2−x}) lattice via ion exchange process with phosphate group. Concentration of SO{sub 4}{sup 2−} ions was varied between X = 0.05–0.5, using (Ca (NO{sub 3}){sub 2}·4H{sub 2}O), ((NH{sub 4}){sub 2}HPO{sub 4}) and (Na{sub 2}SO{sub 4}) as starting materials. X-ray diffraction (XRD), Fourier transform IR spectroscopy (FTIR), showed that the substitution of SO{sub 4}{sup 2−} ions into the lattice resulted in peak broadening and reduced peak height due to the amorphous nature and reduced crystallinity of the resulting HA powder. Transmission electron microscopy (TEM) and field emission electron microscopy (FESEM) analysis confirmed the formation of needle shaped particles of 41 nm size with homogenous and uniform distribution of element within the HA structure.

Characteristics and antioxidant of Ulva intestinalis sulphated polysaccharides extracted with different solvents.

Science.gov (United States)

Peasura, Napassorn; Laohakunjit, Natta; Kerdchoechuen, Orapin; Wanlapa, Sorada

2015-11-01

Ulva intestinalis, a tubular green seaweed, is a rich source of nutrient, especially sulphated polysaccharides. Sulphated polysaccharides from U. intestinalis were extracted with distilled water, 0.1N HCl, and 0.1N NaOH at 80°C for 1, 3, 6, 12, and 24h to study the effect of the extraction solvent and time on their chemical composition and antioxidant activity. Different types of solvents and extraction time had a significant influence on the chemical characteristics and antioxidant activity (pMonosaccharide composition and FT-IR spectra analyses revealed that sulphated polysaccharides from all solvent extractions have a typical sugar backbone (glucose, rhamnose, and sulphate attached at C-2 or C-3 of rhamnose). Sulphated polysaccharides extracted with acid exhibited greater antioxidant activity than did those extracted with distilled water and alkali. The results indicated that solvent extraction could be an efficacious method for enhancing antioxidant activity by distinct molecular weight and chemical characteristic of sulphated polysaccharides. Copyright © 2015 Elsevier B.V. All rights reserved.

Tribological properties of copper-based composites with copper coated NbSe2 and CNT

International Nuclear Information System (INIS)

Chen, Beibei; Yang, Jin; Zhang, Qing; Huang, Hong; Li, Hongping; Tang, Hua; Li, Changsheng

2015-01-01

Graphical abstract: Morphology of copper coated NbSe 2 and CNT; friction coefficient and wear rate of copper-based composites. - Highlights: • NbSe 2 and CNT were coated with copper layers by the means of electroless plating. • The mechanical and tribological properties of copper composites were studied. • The enhancement mechanisms of copper coated NbSe 2 and CNT were proposed. • Copper–copper coated (12 wt.%NbSe 2 –3 wt.%CNT) composite had the best wear resistance. - Abstract: Copper-based composites with copper coated NbSe 2 and/or CNT were fabricated by the powder metallurgy technique. The morphology and phase composition of copper coated NbSe 2 and carbon nanotube (CNT) were observed using high solution transmission electronic microscope (HRTEM), scanning electronic microscope (SEM equipped with EDS) and X-ray diffraction (XRD). The density, hardness, and bending strength of as-prepared copper-based composites were measured, and their tribological properties were investigated using UMT-2 tester. Results indicated that all copper-based composites showed decreased density and bending strength, but increased hardness in comparison with copper matrix. Besides, the incorporation of copper coated NbSe 2 improved the friction-reducing and anti-wear properties of copper matrix. Addition of copper coated CNT greatly enhanced the mechanical and tribological properties. In particular, when the content of copper coated CNT was 3 wt.%, the corresponding composite exhibited the best tribological properties. This was because NbSe 2 was distributed chaotically in matrix, which greatly improved the friction-reducing property of copper, while CNT with superior mechanical strength enhanced the wear resistance by increasing the load-carrying capacity. More importantly, copper layers coated on NbSe 2 and CNT favored the good interfacial combination between fillers and copper matrix showing beneficial effect for the stresses transferring from matrix to fillers

A new route to copper nitrate hydroxide microcrystals

International Nuclear Information System (INIS)

Niu Haixia; Yang Qing; Tang Kaibin

2006-01-01

A solution evaporation route has been successfully developed for the growth of copper nitrate hydroxide microcrystals using copper nitrate solution as the starting material in the absence of any surfactants or templates. The products were characterized by X-ray diffraction (XRD), infrared (IR) spectrum, scanning electron microscopy (SEM) and thermogravimetric (TG) analysis measurements. Controlled experiments suggested that the reaction temperature and solution concentration played an important role on the formation of the products. A possible formation mechanism of the products was also proposed

Radiation-induced grafting of sweet sorghum stalk for copper(II) removal from aqueous solution

International Nuclear Information System (INIS)

Dong, Jing; Hu, Jun; Wang, Jianlong

2013-01-01

Highlights: • Radiation-induced grafting was used to modify the stalk. • Cellulose, hemicellulose and lignin participated in grafting reaction. • Both the structure and composition of stalk had influence on grafting. • The sorption capacity of the grafted stalk increased about five times. -- Abstract: The influence of main components (cellulose, hemicellulose and lignin) of the sweet sorghum stalk on radiation-induced grafting reaction and adsorption of copper from aqueous solution was investigated. Sweet sorghum stalk was grafted with acrylic acid induced by γ-irradiation. The results showed that the grafted stalk contained 1.6 mmol/g carboxyl groups, and its maximal adsorption capacity was 13.32 mg/g. The cellulose, hemicellulose and lignin of the raw materials were confirmed to involve in grafting reaction through comparing the grafting yield and the structure of the grafted materials. Both the structure and the composition of the sweet sorghum stalk had influence on the grafting reaction and adsorption capacity. The adsorption capacity of the grafted sweet sorghum stalk increased about five times, and the adsorption isotherm of the grafted materials conformed to the Langmuir model. The main mechanism for copper adsorption involved in ion exchange

Separation of copper flotation concentrates into density fractions by means of polytungstate aqueous solution

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Luszczkiewicz Andrzej

2016-01-01

Full Text Available Industrial and laboratory flotation copper concentrates were subjected to separation into density fractions by means of heavy liquids in the form of sodium polytungstate aqueous solutions. For two samples, three densities factions were created, however in different density ranges. The density fractions were analyzed to establish the content of copper, lead, silver and organic carbon. The size of particles in both samples was similar (90-95% −0.071 mm. It was found that the lightest density fractions −2.45 and −2.0 g/cm3 still contained sulfide minerals scattered in the organic carbon bearing particles. Removal of the lightest density fraction (−2.0 g/cm3 from the industrial concentrate samples led to considerable reduction of organic carbon (92% and increasing its quality from 13 to 28% Cu. The mineralogical analysis of the heavy liquid separation products showed that most sulfide minerals were evenly dissemination in the heaviest density fractions with the recovery of 95-98%. The lightest density fraction of −2.0 g/cm3, being the richest in organic carbon, contained approximately 3% of unliberated sulfide minerals.

Optical properties of stabilized copper nanoparticles

Energy Technology Data Exchange (ETDEWEB)

Mohindroo, Jeevan Jyoti, E-mail: jjmdav@gmail.com [Punjab Technical University, Kapurthala Punjab (India); Department of Chemistry, DAV College, Amritsar, Punjab India (India); Garg, Umesh Kumar, E-mail: Umeshkgarg@gmail.com [Punjab Technical University, Kapurthala Punjab (India); Guru Teg Bahadur Khalsa College of IT, Malout, Punjab (India); Sharma, Anshul Kumar [Department of Physics, Guru Nanak Dev University, Amritsar 143005 (India)

2016-05-06

Optical studies involving calculation of Band Gap of the synthesized copper nanoparticles were carried out in the wavelength range of 500 to 650 nm at room temperature, the particles showed high absorption at 550 nm indicating their good absorptive properties. In this method water is used as the medium for reduction of copper ions in to copper Nanoparticles the stabilization of copper Nanoparticles was studied with starch both as a reductant and stabilizer,. The reaction mixture was heated using a kitchen microwave for about 5 minutes to attain the required temp for the reaction. The pH of the solution was adjusted to alkaline using 5% solution of NaOH. Formation of Copper Nanoparticles was indicated by change in color of the solution from blue to yellowish black which is supported by the UV absorption at 570 nm.the synthesized particles were washed with water and alcohol. The optical properties depend upon absorption of radiations which in turn depends upon ratio of electrons and holes present in the material and also on the shape of the nanoparticles. In the present investigation it was observed that optical absorption increases with increase in particle size. The optical band gap for the Nanoparticles was obtained from plots between hv vs. (αhv){sup 2} and hv vs. (αhv){sup 1/2}. The value of Band gap came out to be around 1.98–2.02 eV which is in close agreement with the earlier reported values.

New Approach to Remove Metals from Chromated Copper Arsenate (CCA)-Treated Wood

Science.gov (United States)

Todd F. Shupe; Chung Y. Hse; Hui Pan

2012-01-01

Recovery of metals from chromated copper arsenate (CCA)-treated southern pine wood particles was investigated using binary acid solutions consisting of acetic, oxalic, and phosphoric acids in a microwave reactor. Formation of an insoluble copper oxalate complex in the binary solution containing oxalic acid was the major factor for low copper removal. Furthermore, the...

Electrodeposition of copper from a copper sulfate solution using a packed-bed continuous-recirculation flow reactor at high applied electric current

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Meshaal F. Alebrahim

2015-09-01

Full Text Available The purpose of this study is mainly to investigate the performance of a packed-bed continuous-recirculation flow reactor at high applied electric current in removing copper, Cu(II, from simulated electrolyte by electrodeposition. The effects of pHo, circulation rate of flow, initial copper concentration, intensity of the applied current and the method of application of electric current, as to have a constant value during all the time of electrolysis or to be decreased with time, on copper electrodeposition and current efficiency are revealed. The results showed that the increase in pH (provided not lead to the deposition of Cu(OH2, initial concentration of the copper and flow rate increased the electrodeposition of copper as well as improved current efficiency. However, increasing intensity of the applied electric current led to an increase in the electrodeposition of copper and decreased electrical efficiency. It was also observed that reducing the intensity of applied electric current with time during the electrolysis process while maintaining other operating variables constant led to a significant reduction in the consumption of electrical energy used in the process of copper removal by electrodeposition; a reduction of 41.6% could be achieved.

Activation determination of copper in food

International Nuclear Information System (INIS)

Jiranek, V.; Bludovsky, R.

1982-01-01

Neutron activation analysis was used for determining copper content in food. Analyzed were dried milk, flour, coffee, tea, husked rice, and liver. Bowen's kale powder with a guaranteed copper content of 3.6 to 6.5 ppm was used as a reference biological material. The instruments, chemicals and solutions used are reported. The method is described of copper separation with α-benzoinoxime and pyridine as is the procedure for the destructive activation analysis of samples. The copper concentrations in the foods under analysis were found to range within usual limits. The copper concentration determined in the reference material agreed with the measured value. The analysis confirms that the method yields reliable results. (J.B.)

Sulfidation treatment of copper-containing plating sludge towards copper resource recovery.

Science.gov (United States)

Kuchar, D; Fukuta, T; Onyango, M S; Matsuda, H

2006-11-02

The present study is concerned with the sulfidation treatment of copper-containing plating sludge towards copper resource recovery by flotation of copper sulfide from treated sludge. The sulfidation treatment was carried out by contacting simulated or real copper plating sludge with Na(2)S solution for a period of 5 min to 24 h. The initial molar ratio of S(2-) to Cu(2+) (S(2-) to Me(2+) in the case of real sludge) was adjusted to 1.00, 1.25 or 1.50, while the solid to liquid ratio was set at 1:50. As a result, it was found that copper compounds were converted to various copper sulfides within the first 5 min. In the case of simulated copper sludge, CuS was identified as the main sulfidation product at the molar ratio of S(2-) to Cu(2+) of 1.00, while Cu(7)S(4) (Roxbyite) was mainly found at the molar ratios of S(2-) to Cu(2+) of 1.50 and 1.25. Based on the measurements of oxidation-reduction potential, the formation of either CuS or Cu(7)S(4) at different S(2-) to Cu(2+) molar ratios was attributed to the changes in the oxidation-reduction potential. By contrast, in the case of sulfidation treatment of real copper sludge, CuS was predominantly formed, irrespective of S(2-) to Me(2+) molar ratio.

Magnesium sulphate and amiodarone prophylaxis for prevention of postoperative arrhythmia in coronary by-pass operations

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Huysal Kagan

2009-02-01

Full Text Available Abstract Background The aim of this study was to investigate the use of prophylactic magnesium sulphate and amiodarone in treating arrhythmias that may occur following coronary bypass grafting operations. Methods The study population consisted of 192 consecutive patients who were undergoing coronary artery bypass grafting (CABG. Sixty-four patients were given 3 g of magnesium sulphate (MgSO4 [20 ml = 24.32 mEq/L Mg+2] in 100 cc of isotonic 0.9% solution over 2 hours intravenously at the following times: 12 hours prior to the operation, immediately following the operation, and on postoperative days 1, 2, and 3 (Group 1. Another group of 64 patients was given a preoperative infusion of amiodarone (1200 mg on first post-operative day (Group 2. After the operation amiodarone was administered orally at a dose of 600 mg/day. Sixty-four patients in group 3 (control group had 100 cc. isotonic 0.9% as placebo, during the same time periods. Results In the postoperative period, the magnesium values were significantly higher in Group 1 than in Group 2 for all measurements. The use of amiodarone for total arrhythmia was significantly more effective than prophylactic treatment with magnesium sulphate (p = 0.015. There was no difference between the two drugs in preventing supraventricular arrhythmia, although amiodarone significantly delayed the revealing time of atrial fibrillation (p = 0.026. Ventricular arrhythmia, in the form of ventricular extra systole, was more common in the magnesium prophylaxis group. The two groups showed no significant differences in other operative or postoperative measurements. No side effects of the drugs were observed. Conclusion Prophylactic use of magnesium sulphate and amiodarone are both effective at preventing arrhythmia that may occur following coronary by-pass operations. Magnesium sulphate should be used in prophylactic treatment since it may decrease arrhythmia at low doses. If arrhythmia should occur despite this

Anodic behaviour of the stainless steel AISI 430 in aqueous solutions of chloride and sulphate ions

International Nuclear Information System (INIS)

Sebrao, M.Z.

1982-01-01

The kinetics of the dissolution of stainless steel AISI 430 in the presence of chloride and sulphate ions has been studied in terms of the ion concentration, the pH variation, and the velocity of the working electrode. The experimental method utilized was the potentiostatic anodic polarization, and the reactants used were NaCl and Na 2 SO 4 at room temperature. Atomic Absorption spectrophotometry and Auger Electrons spectroscopy (AES) analyses were made in order to support the interpretation of results obtained by means of the potentiostatic polarization method. (author)

A new method to measure effective soil solution concentration predicts copper availability to plants.

Science.gov (United States)

Zhang, H; Zhao, F J; Sun, B; Davison, W; McGrath, S P

2001-06-15

Risk assessments of metal contaminated soils need to address metal bioavailability. To predict the bioavailability of metals to plants, it is necessary to understand both solution and solid phase supply processes in soils. In striving to find surrogate chemical measurements, scientists have focused either on soil solution chemistry, including free ion activities, or operationally defined fractions of metals. Here we introduce the new concept of effective concentration, CE, which includes both the soil solution concentration and an additional term, expressed as a concentration, that represents metal supplied from the solid phase. CE was measured using the technique of diffusive gradients in thin films (DGT) which, like a plant, locally lowers soil solution concentrations, inducing metal supply from the solid phase, as shown by a dynamic model of the DGT-soil system. Measurements of Cu as CE, soil solution concentration, by EDTA extraction and as free Cu2+ activity in soil solution were made on 29 different soils covering a large range of copper concentrations. Theywere compared to Cu concentrations in the plant material of Lepidium heterophyllum grown on the same soils. Plant concentrations were linearly related and highly correlated with CE but were more scattered and nonlinear with respect to free Cu2+ activity, EDTA extraction, or soil solution concentrations. These results demonstrate that the dominant supply processes in these soils are diffusion and labile metal release, which the DGT-soil system mimics. The quantity CE is shown to have promise as a quantitative measure of the bioavailable metal in soils.

Dissolution of copper and iron from malachite ore and precipitation of copper sulfate pentahydrate by chemical process

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H. Kokes

2014-03-01

Full Text Available The present work describes an investigation of a chemical process for the recovery of copper and iron from malachite ore. For the dissolution of copper and iron, H2SO4 was employed as well as H2O2 as an oxidizing agent. The effects of reaction temperature and time, acid concentration, liquid-to-solid ratio and agitation rate on the copper and iron percentage were investigated. Following the steps of dissolving the copper and iron sulfate and filtering, iron (III hydroxide was precipitated by adjusting the pH level of the solution. Subsequently, copper sulfate pentahydrate was obtained by using various precipitants (i.e. ethanol, methanol and sulfuric acid.

SOLUBILITIES AND PHYSICAL PROPERTIES OF SATURATED SOLUTIONS IN THE COPPER SULFATE + SULFURIC ACID + SEAWATER SYSTEM AT DIFFERENT TEMPERATURES

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F. J. Justel

2015-09-01

Full Text Available AbstractIn Chile, the most important economic activity is mining, concentrated in the north of the country. This is a desert region with limited water resources; therefore, the mining sector requires research and identification of alternative sources of water. One alternative is seawater, which can be a substitute of the limited fresh water resources in the region. This work determines the influence of seawater on the solid-liquid equilibrium for acid solutions of copper sulfate at different temperatures (293.15 to 318.15 K, and its effect on physical properties (density, viscosity, and solubility. Knowledge of these properties and solubility data are useful in the leaching process and in the design of copper sulfate pentahydrate crystallization plants from the leaching process using seawater by means of the addition of sulfuric acid.

Determination of Cu(III) and Cu(II)+Cu(III) in superconducting copper ceramics

International Nuclear Information System (INIS)

Nedelcheva, T.; Kostadinova, L.; Stoyanova-Ivanova, A.; Ivanova, I.

1992-01-01

Copper(III) and total copper in superconducting Y-Ba-Cu oxide and related compounds can be determinated by two successive iodimetric titrations after the sample has been dissolved under Ar in HCl/KI medium. First, the iodine equivalent to copper(III) is titrated with Na 2 S 2 O 3 solution at pH 4.8, copper(II) being masked with EDTA. The total copper is then determined in the same solution by demasking with acid and iodide, followed by iodimetric titration. The method is both accurate and reproducible. The relative standard deviations for 1.074% copper(III) and 23.37% total copper are 0.8% and 0.3%, respectively. (orig.)

Photochemical synthesis of copper nanoparticles incorporated in poly(vinyl pyrrolidone)

International Nuclear Information System (INIS)

Giuffrida, Salvatore; Costanzo, Lucia L.; Ventimiglia, Giorgio; Bongiorno, Corrado

2008-01-01

The effect of the presence of poly(vinyl pyrrolidone) (PVP) on the copper nanoparticle formation, obtained by UV irradiation of ethanol solution of Cu(acac) 2 (acac = 2,4-pentanedionato), was investigated. At 254 nm, in conditions of light completely absorbed by complex, the PVP exhibited protective and stabilizing effects, as shown by the formation of a colloidal copper solution and by a block of the heterogeneous process, which leads to thin film formation on the quartz walls. The colloidal solution was tested for several months by plasmon position and it was found that it remained unaltered in inert atmosphere, but returned to the starting complex on contact with air. The PVP ability to control the particle size was investigated by carrying out photoreduction sensitized by Hacac at 254 and 300 nm, in the presence of PVP concentration varying from 0 to 0.2 M. In this range it was possible to obtain copper nanoparticles of dimensions decreasing from 30 to 4 nm. Besides this, the PVP (0.005-0.05 M) role as sensitizer was investigated by irradiating solutions of Cu(acac) 2 at 300 nm which is an inactive wavelength for copper reduction by direct light absorption. It was found that the PVP was an efficient sensitizer of the copper photoreduction. The nanoparticles were characterized by plasmon band, Trasmission Electron Microscope (TEM) as well as Dynamic Light Scattering (DSL) analysis. The overall results evidence the advantages of the PVP use in the nanoparticle copper formation through the photochemical technique such as the exclusive formation of colloidal copper, their size control, stable colloidal solution and complete return to the starting complex.

Evaluation of a single-dose of intravenous magnesium sulphate for prevention of postoperative pain after inguinal surgery

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Shashi Kiran

2011-01-01

Full Text Available This study was undertaken to study efficacy of single dose of intravenous magnesium sulphate to reduce post-operative pain in patients undergoing inguinal surgery. One hundred patients undergoing inguinal surgery were divided randomly in two groups of 50 each. The patients of magnesium sulphate group (Group-I received magnesium sulphate 50 mg/kg in 250 ml of isotonic sodium chloride solution IV whereas patients in control group (Group-II received same volume of isotonic sodium chloride over 30 minutes preoperatively. Anaesthesia was induced with propofol (2 mg/kg and pethidine (1 mg/kg. Atracurium besylate (0.5 mg/kg was given to facilitate insertion of LMA. Pain at emergence from anaesthesia and 2, 4, 6, 12 and 24 hours after surgery was evaluated. The timing and dosage of rescue analgesic during first 24 hrs after operation was noted. Pain in postop period was significantly lower in magnesium sulphate group in comparison to control group at emergence from anaesthesia and 2, 4, 6, 12 and 24 hrs postop [1.86 vs. 1.96 (P=0.138, 1.22 vs. 1.82 (P=0.001, 1.32 vs. 1.88 (P=0.000, 2.74 vs. 3.84 (P=0.000, 1.36 vs. 2.00 (P=0.000 and 0.78 vs 1.30 (P=0.000, respectively]. Patients in group-I were more sedated as compared to group-II [sedation score 1.86 vs. 1.40 (P=0.000]. Rescue analgesia requirement postoperatively in first 4, 8 and 16 hrs was significantly lower in patients of group-1 than in group- II [1.9 vs. 3.8 (P<0.05, 25.50 vs. 52.50 (P<0.05 and 0.000 vs. 7.5 (P<0.05]. Preoperative magnesium sulphate infusion decreases postop pain and requirement of rescue analgesia.

Dose-response testing with nickel sulphate using the TRUE test in nickel-sensitive individuals. Multiple nickel sulphate patch-test reactions do not cause an 'angry back'

DEFF Research Database (Denmark)

Andersen, Klaus Ejner; Lidén, C; Hansen, J

1993-01-01

The aim of this study was to employ the TRUE test assay to confirm the presence or absence of the 'angry back' phenomenon, i.e. that a strong positive patch-test reaction heightens adjacent patch-test response. In addition, we wished to establish the dose-response relationship for nickel sulphate...... back' phenomenon was not apparent in this study, as the spill-over effect was not statistically significant. Strong reactions to high concentrations of nickel sulphate did not enhance the response to adjacent lower concentrations of nickel sulphate....

Preparation of copper nanoparticles by radiation

International Nuclear Information System (INIS)

Liu Yajian; Guo Xiongbin; Li Zhaolong; Fu Junjie; Tan Yuanyuan; Zhou Xinyao; Xu Furong

2013-01-01

Copper nanoparticles were successfully synthesized by 60 Co-γ radiation with aqueous solution of cupric sulfate under inert nitrogen-purged conditions. Cu nanoparticles were characterized by using X-ray diffraction (XRD), transmission electron microscopy (TEM), laser particle size distribution analyzer (LSPSDA) and differential scanning calorimeter (DSC) techniques, respectively. The effects of solution system, pH, additive of surfactant and absorbed doses on the particle size and its distribution as well as stored stability of Cu naoparticles were investigated. High resolution TEM pictures showed the formation of homogeneous cubic-structured copper nanoparticles with different sizes depends on the synthetic conditions. This new kind of synthesis method shows the excellent stability, which may provide an efficient way to improve the fine tuning of the structure and size of copper nanoparticles. (authors)

Comparison of amiodarone vs magnesium sulphate in the prevention of atrial fibrillation after coronary artery bypass grafting surgery

International Nuclear Information System (INIS)

Bashir, I.; Abbas, S.

2013-01-01

Background: Atrial fibrillation (AF) is common in patients after coronary artery bypass grafting (CABG) and can result in increased morbidity and mortality, increased length of hospital stay, and increased cost. In this study we compared the efficacy of amiodarone versus magnesium sulphate in the prophylaxis of post-CABG atrial fibrillation. Objective: This study was carried out to assess the efficacy of amiodarone in comparison to magnesium sulphate in the prevention of atrial fibrillation after coronary artery bypass grafting. Study Design: Randomized controlled trials. Place and duration of study: The study was carried out at Armed Forces Institute of Cardiology and National Institute of Heart Diseases, Rawalpindi from July 2010 to December 2011 Patients and Methods: Total 240 patients were included in the study and randomly divided in two groups of 120 each using random number table. Patients in Group A (Amiodarone group) were given a loading dose of amiodarone 5 mg/Kg after induction of anesthesia which was then continued as infusion at 5 micro gm/Kg/minute on first postoperative day. This was followed by an oral dose of 600 mg/day postoperatively for 5 days. Those in Group B (Magnesium Sulphate group) received 2 g of magnesium sulphate in 100 ml of isotonic 0.9% solution intravenously over 1 hour at following times: preoperatively, immediately following the operation, and on postoperative days 1, 2, and 3. Results: Thirteen patients (10.8%) developed AF in Amiodarone group, compared to 31 patients (25.8%) in magnesium sulphate group. The results proved amiodarone to be more effective than magnesium sulphate in preventing post-CABG AF (p<0.001). Thirty one patients who developed AF postoperatively in the magnesium group were treated with amiodarone, and all patients recovered normal sinus rhythm. In the amiodarone prophylaxis group, 9 patients regained sinus rhythm in 6 - 8 hours, while for 4 remaining patients cardioversion was attempted out of which 2

Corrosion Performance of Inconel 625 in High Sulphate Content

Science.gov (United States)

Ismail, Azzura

2016-05-01

Inconel 625 (UNS N06625) is a type of nickel-chromium-molybdenum alloy with excellent corrosion resistance in a wide range of corrosive media, being especially resistant to pitting and crevice corrosion. However, in aggressive environment, Inconel 625 will suffer corrosion attack like other metals. This research compared the corrosion performance of Inconel 625 when exposed to higher sulphate content compared to real seawater. The results reveal that Inconel 625 is excellent in resist the corrosion attack in seawater. However, at increasing temperature, the corrosion resistance of this metal decrease. The performance is same in seawater with high sulphate content at increasing temperature. It can be concluded that sulphate promote perforation on Inconel 625 and become aggressive agents that accelerate the corrosion attack.

Effects of Copper-based Compounds, Antibiotics and a Plant Activator on Population Sizes and Spread of Clavibacter michiganensis subsp. michiganensis in Greenhouse Tomato Seedlings

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Svetlana Milijašević

2009-01-01

Full Text Available Three copper-based compounds (copper hydroxide, copper oxychloride, copper sulphate, two antibiotics (streptomycin and kasugamycin and a plant activator (ASM significantly reduced population sizes and spread of C. michiganensis subsp. michiganensis among tomatoseedlings in the greenhouse. Streptomycin had the best effect in reducing pathogen population size in all sampling regions. Moreover, this antibiotic completely stopped the spread of C. michiganensis subsp. michiganensis in the region most distant from the inoculumfocus. Copper hydroxide mixed with streptomycin significantly limited the pathogen population, compared with copper hydroxide alone, the other copper-based compounds, ASM and kasugamycin. However, combining streptomycin with copper hydroxide did notcontribute to its greater efficacy against the pathogen population. Copper-based compounds, in general, were less effective in limiting pathogen population sizes than the other treatments in all three sampling regions, primarily copper oxychloride and the combinationof copper hydroxide and mancozeb. Among copper compounds, copper hydroxide was the most prominent in reducing the bacterial population, especially in the region closest to the inoculum focus, while its combination with mancozeb did not improve the effects. Kasugamycin significantly limited pathogen population size, compared to copper bactericides, but it was less effective than the other antibiotic compound, i.e. streptomycin. The plant activator ASM significantly reduced population density, and it was more effectivewhen used three days prior to inoculation than six days before inoculation.

Analysis of the hygroscopic and volatile properties of ammonium sulphate seeded and un-seeded SOA particles

Science.gov (United States)

Meyer, N. K.; Duplissy, J.; Gysel, M.; Metzger, A.; Dommen, J.; Weingartner, E.; Alfarra, M. R.; Fletcher, C.; Good, N.; McFiggans, G.; Jonsson, Ã. M.; Hallquist, M.; Baltensperger, U.; Ristovski, Z. D.

2008-05-01

The volatile and hygroscopic properties of ammonium sulphate seeded and un-seeded secondary organic aerosol (SOA) derived from the photo-oxidation of atmospherically relevant concentrations of α-pinene were studied. The seed particles were electrospray generated ammonium sulphate ((NH4)2SO4) having diameters of approximately 33 nm with a quasi-mono-disperse size distribution (geometric standard deviation σg=1.3). The volatile and hygroscopic properties of both seeded and unseeded SOA were simultaneously measured with a VH-TDMA (volatility - hygroscopicity tandem differential mobility analyzer). VH-TDMA measurements of unseeded SOA show a decrease in the hygroscopic growth (HGF) factor for increased volatilisation temperatures such that the more volatile compounds appear to be more hygroscopic. This is opposite to the expected preferential evaporation of more volatile but less hygroscopic material, but could also be due to enhanced oligomerisation occurring at the higher temperature in the thermodenuder. In addition, HGF measurements of seeded SOA were measured as a function of time at two relative humidities, below (RH 75%) and above (RH 85%) the deliquescence relative humidity (DRH) of the pure ammonium sulphate seeds. As these measurements were conducted during the onset phase of photo-oxidation, during particle growth, they enabled us to find the dependence of the HGF as a function of the volume fraction of the SOA coating. HGF's measured at RH of 85% showed a continuous decrease as the SOA coating thickness increased. The measured growth factors show good agreements with ZSR predictions indicating that, at these RH values, there are only minor solute-solute interactions. At 75% RH, as the SOA fraction increased, a rapid increase in the HGF was observed indicating that an increasing fraction of the (NH4)2SO4 is subject to a phase transition, going into solution, with an increasing volume fraction of SOA. To our knowledge this is the first time that SOA derived

Development of poly(aspartic acid-co-malic acid) composites for calcium carbonate and sulphate scale inhibition.

Science.gov (United States)

Mithil Kumar, N; Gupta, Sanjay Kumar; Jagadeesh, Dani; Kanny, K; Bux, F

2015-01-01

Polyaspartic acid (PSI) is suitable for the inhibition of inorganic scale deposition. To enhance its scale inhibition efficiency, PSI was modified by reacting aspartic acid with malic acid (MA) using thermal polycondensation polymerization. This reaction resulted in poly(aspartic acid-co-malic acid) (PSI-co-MA) dual polymer. The structural, chemical and thermal properties of the dual polymers were analysed by using scanning electron microscopy, Fourier transform infrared spectroscopy, X-ray diffraction, differential scanning calorimetry and gel permeation chromatography. The effectiveness of six different molar ratios of PSI-co-MA dual polymer for calcium carbonate and calcium sulphate scale inhibition at laboratory scale batch experiments was evaluated with synthetic brine solution at selected doses of polymer at 65-70°C by the static scale test method. The performance of PSI-co-MA dual polymer for the inhibition of calcium carbonate and calcium sulphate precipitation was compared with that of a PSI single polymer. The PSI-co-MA exhibited excellent ability to control inorganic minerals, with approximately 85.36% calcium carbonate inhibition and 100% calcium sulphate inhibition at a level of 10 mg/L PSI-co-MA, respectively. Therefore, it may be reasonably concluded that PSI-co-MA is a highly effective scale inhibitor for cooling water treatment applications.

An electrochemical study of the effect of nitrate and sulphate on the corrosion behaviour of Magnox AL80 in pond environments

International Nuclear Information System (INIS)

Tyfield, S.P.; Martin, F.

1987-04-01

The open circuit rest potential and the cyclic potentiodynamic polarisation behaviour of abraded Magnox AL80 has been studied at 22 0 C in sodium hydroxide solutions (200 gm -3 , pH ∼ 11.6) dosed separately and with a combination of chloride and nitrate. The results are considered in terms of the effect of the presence of nitrate on the initiation of localised breakdown of the passive film on Magnox AL80. A similar study of the effect of the presence of sulphate in the sodium hydroxide medium (200 gm -3 ) is described and the aggressivity of sulphate is compared to that of chloride. (author)

The effect of water on the sulphation of limestone

Energy Technology Data Exchange (ETDEWEB)

Chunbo Wang; Lufei Jia; Yewen Tan; E.J. Anthony [North China Electric Power University, Baoding City (China). School of Energy and Power Engineering

2010-09-15

A series of tests was conducted in a thermogravimetric analyzer (TGA) to study the sulphation behaviour of limestone in the presence of water over the temperature range of 800-850{sup o}C. Four different Canadian limestones, all with a particle size range of 75-425 {mu}m, were sulphated using a synthetic flue gas with a composition of 15% CO{sub 2}, 3% O{sub 2}, 0% or 10% H{sub 2}O, 1750 ppm SO{sub 2} and the balance N{sub 2}. Water was shown to have a significant promotional effect on sulphation, especially in the diffusion-controlled stage. However, the effect of water during the kinetic-controlled stage appeared to be much less pronounced. Based on these results, it is proposed that the presence of water leads to the transient formation of Ca(OH){sub 2} as an intermediate, which in turn reacts with SO{sub 2} at a faster rate than CaO does. Alternatively stated, it appears that H{sub 2}O acts as catalyst for the sulphation reaction of CaO. 30 refs., 8 figs., 3 tabs.

The action of diazoxide and minoxidil sulphate on rat blood vessels: a comparison with cromakalim.

Science.gov (United States)

Newgreen, D. T.; Bray, K. M.; McHarg, A. D.; Weston, A. H.; Duty, S.; Brown, B. S.; Kay, P. B.; Edwards, G.; Longmore, J.; Southerton, J. S.

1990-01-01

1. The actions of diazoxide and minoxidil sulphate have been compared with those of cromakalim in rat aorta and portal vein. 2. Diazoxide and minoxidil sulphate hyperpolarized the rat portal vein in a similar manner to cromakalim. 3. Cromakalim, diazoxide and minoxidil sulphate increased 42K and 86Rb efflux from rat portal vein, although minoxidil sulphate had only a small effect on 86Rb efflux. 4. Cromakalim, diazoxide and minoxidil sulphate increased 42K efflux from rat aorta but only cromakalim and diazoxide increased 86Rb efflux from this tissue. 5. Glibenclamide inhibited the relaxant actions of cromakalim, diazoxide and minoxidil sulphate on rat aorta and the increase in 42K efflux produced by these agents in this tissue. 6. Diazoxide relaxed an 80 mM KCl-induced contraction of rat aorta, whilst cromakalim and minoxidil sulphate were without effect. 7. Cromakalim, diazoxide and minoxidil sulphate had no effect on cyclic AMP or cyclic GMP concentrations in rat aorta. 8. It is concluded that diazoxide and minoxidil sulphate like cromakalim exhibit K+ channel opening properties in vascular smooth muscle. Diazoxide exerts an additional inhibitory action not related to the production of cyclic AMP or cyclic GMP. The action of minoxidil sulphate may be primarily located at a K+ channel which is relatively impermeable to 86Rb. PMID:2167738

ENVIRONMENTAL RISK ASSESSMENT OF SOME COPPER BASED FUNGICIDES ACCORDING TO THE REQUIREMENTS OF GOOD LABORATORY PRACTICE

Directory of Open Access Journals (Sweden)

Marga GRĂDILĂ

2015-10-01

Full Text Available The paper presents data demonstrating the functionality of biological systems reconstituted with aquatic organisms developed under Good Laboratory Practice testing facility within Research - Development Institute for Plant Protection Bucharest for environmental risk assessment of four fungicides based on copper, according to Good Laboratory Practice requirements. For risk assessment, according to GLP were made the following steps: Good Laboratory Practice test facility was established, we have ensured adequate space for growth, acclimatization and testing for each test species, it was installed a complex water production instalation needed to perform tests, it was achieved control system for checking environmental conditions and have developed specific operating procedures that have been accredited according to Good Laboratory Practice.The results showed that biological systems model of the Good Laboratory Practice test facility in Research - Development Institute for Plant Protection meet the requirements of Organisation for Economic Co-operation and Development Guidelines regarding GLP, and after testing copper-based fungicides in terms of acute toxicity Cyprinus carpio and to Daphnia magna revealed that three of them (copper oxychloride, copper hydroxide and copper sulphate showed ecological efficiency, ie low toxicity. Metallic copper based fungicides showed a higher toxicity, resulting in fish toxicity symptoms: sleep, sudden immersion, faded, weakness, swimming in spiral, lack of balance, breathing slow and cumbersome, spasms and mortality.

Blood biochemical changes in common carp (Cyprinus carpio Linnaeus, 1758 fed different levels of copper sulphate and zeolite

Directory of Open Access Journals (Sweden)

Arzu Aydın Uncumusaoğlu

2018-02-01

Full Text Available In this study, copper toxicity, was investigated after the addition of zeolite to the diet of common carps (Cyprinus carpio. The experiment included four groups with three replicates each. The 4 group feeds were [CuSO4; CuSO4 + Zeolite; Zeolite, and the control without CuSO4 or Zeolite with three replicates each. Fishes were kept in 80 L glass aquariums with 10 fishes with a mean weight of 60.6 ± 0.2 g. At the end of each period, a necropsy was performed on fishes from each treatment, and gross clinical signs were recorded. We found significant changes in the blood parameters of the common carps with or without different levels of zeolite and copper. Changes in cholesterol (CHOL, triglyceride (TG, low density lipoprotein (LDL, alanine aminotransferase (ALT, aspartate aminotransferase (AST, alkaline phosphatase (ALP, calcium (Ca2+, phosphorus (P+, sodium (Na+, potassium (K+, chloride (Cl-, magnesium (Mg2+, and ferrous (Fe+2 were also significant. Our results suggest that zeolite can be used in fish feeds at a rate of 40 mg/l to mitigate the toxic effects of copper.

Corrosion study on high power feeding of telecomunication copper cable in 5 wt.% CaSO4.2H2O solution

Science.gov (United States)

Shamsudin, Shaiful Rizam; Hashim, Nabihah; Ibrahim, Mohd Saiful Bahri; Rahman, Muhammad Sayuzi Abdul; Idrus, Muhammad Amin; Hassan, Mohd Rezadzudin; Abdullah, Wan Razli Wan

2016-07-01

The studies were carried out to find out the best powering scheme over the copper telephone line. It was expected that the application of the higher power feeding could increase the data transfer and capable of providing the customer's satisfaction. To realize the application of higher remote power feeding, the potential of corrosion problem on Cu cables was studied. The natural corrosion behaviour of copper cable in the 0.5% CaSO4.2H2O solution was studied in term of open circuit potential for 30 days. The corrosion behaviour of higher power feeding was studied by the immersion and the planned interval test to determine the corrosion rate as well as the effect of voltage magnitudes and the current scheme i.e. positive direct (DC+) and alternating current (AC) at about 0.40 ± 0.01 mA/ cm2 current density. In the immersion test, both DC+ and AC scheme showed the increasing of feeding voltage magnitude has increased the corrosion rate of Cu samples starting from 60 to 100 volts. It was then reduced at about 100 - 120 volts which may due to the passive and transpassive mechanism. The corrosion rate was slowly reduced further from 120 to 200 volts. Visually, the positively charged of Cu cable was seems susceptible to severe corrosion, while AC scheme exhibited a slight corrosion reaction on the surface. However, the planned interval test and XRD results showed the corrosion activity of the copper cable in the studied solution was a relatively slow process and considered not to be corroded as a partially protective scale of copper oxide formed on the surface.

Nucleation and growth of copper phthalocyanine aggregates deposited from solution on planar surfaces

Energy Technology Data Exchange (ETDEWEB)

Ghani, Fatemeh [Department of Theory & Bio-Systems, Max Planck Institute of Colloids and Interfaces, Am Mühlenberg 1 Golm, 14476 Potsdam (Germany); Gojzewski, Hubert, E-mail: hubert.gojzewski@put.poznan.pl [Department of Theory & Bio-Systems, Max Planck Institute of Colloids and Interfaces, Am Mühlenberg 1 Golm, 14476 Potsdam (Germany); Institute of Physics, Poznan University of Technology, Piotrowo 3, 60-965 Poznan (Poland); Riegler, Hans [Department of Theory & Bio-Systems, Max Planck Institute of Colloids and Interfaces, Am Mühlenberg 1 Golm, 14476 Potsdam (Germany)

2015-10-01

Graphical abstract: - Highlights: • Copper phthalocyanine deposited on planar surfaces by 3 solution process methods. • Aggregate morphology examined for coverage extending over 3 orders of magnitude. • Morphologies vary from small individual domains to mesh-like multilayers. • Nucleation and growth model explains the observed deposit morphologies. - Abstract: Copper phthalocyanine (CuPc) dissolved in trifluoroacetic acid (TFA) is deposited on solid SiO{sub 2} surfaces by solvent evaporation. The deposited CuPc aggregates are investigated by atomic force microscopy (AFM). The CuPc deposits were prepared by spin casting, dip coating, and spray deposition. Depending on the amount of deposited CuPc the aggregate morphology ranges from small individual domains to mesh-like multilayers. Each domain/layer consists of many parallel stacks of CuPc molecules with the square, plate-like molecules piled face-wise within each stack. The parallel stacks are attached sideways (i.e., edgewise attachment molecularly) to the substrate forming “nanoribbons” with uniform thickness of about 1 nm and varying width. The thickness reflects the length of a molecular edge, the width the number of stacks. A nucleation and growth model is presented that explains the observed aggregate and multilayer morphologies as result of the combination of nucleation, transport processes and a consequence of the anisotropic intermolecular interactions due to the shape of the CuPc molecule.

High-mobility solution-processed copper phthalocyanine-based organic field-effect transistors

Directory of Open Access Journals (Sweden)

Nandu B Chaure, Andrew N Cammidge, Isabelle Chambrier, Michael J Cook, Markys G Cain, Craig E Murphy, Chandana Pal and Asim K Ray

2011-01-01

Full Text Available Solution-processed films of 1,4,8,11,15,18,22,25-octakis(hexyl copper phthalocyanine (CuPc6 were utilized as an active semiconducting layer in the fabrication of organic field-effect transistors (OFETs in the bottom-gate configurations using chemical vapour deposited silicon dioxide (SiO2 as gate dielectrics. The surface treatment of the gate dielectric with a self-assembled monolayer of octadecyltrichlorosilane (OTS resulted in values of 4×10−2 cm2 V−1 s−1 and 106 for saturation mobility and on/off current ratio, respectively. This improvement was accompanied by a shift in the threshold voltage from 3 V for untreated devices to -2 V for OTS treated devices. The trap density at the interface between the gate dielectric and semiconductor decreased by about one order of magnitude after the surface treatment. The transistors with the OTS treated gate dielectrics were more stable over a 30-day period in air than untreated ones.

Extraction of uranium from coarse ore and acid-curing and ferric sulphate-trickle leaching process

International Nuclear Information System (INIS)

Jin Suoqing

1994-01-01

On the basis of analysis of the problems in the technology of the traditional uranium hydrometallurgy and the limitations of thin layer leaching process (TLL), a new leaching system-acid-curing and ferric sulphate-trickle leaching (AFL) process (NGJ in Chinese) has developed for extraction of uranium from the coarse ore. The ferric sulphate solution was used for trickling the acid-cured uranium ore and the residual leaching reaction incomplete in TLL process can be improved in this process. And the AFL process has a wide applicability to China's uranium ores, being in competition with the traditional agitation leaching process for treating coarse ores. The uranium ore processing technology based on the AFL process will become one of the new basic technologies of uranium hydrometallurgy. A series of difficulties will be basically overcome associated with fine grinding because of its elimination in the presented process. Moreover, the situation of the present uranium hydrometallurgy can be also changed owing to without technological effluent discharge

Enrichment of copper and recycling of cyanide from copper-cyanide waste by solvent extraction

Science.gov (United States)

Gao, Teng-yue; Liu, Kui-ren; Han, Qing; Xu, Bin-shi

2016-11-01

The enrichment of copper from copper-cyanide wastewater by solvent extraction was investigated using a quaternary ammonium salt as an extractant. The influences of important parameters, e.g., organic-phase components, aqueous pH values, temperature, inorganic anion impurities, CN/Cu molar ratio, and stripping reagents, were examined systematically, and the optimal conditions were determined. The results indicated that copper was effectively concentrated from low-concentration solutions using Aliquat 336 and that the extraction efficiency increased linearly with increasing temperature. The aqueous pH value and concentrations of inorganic anion impurities only weakly affected the extraction process when varied in appropriate ranges. The CN/Cu molar ratio affected the extraction efficiency by changing the distribution of copper-cyanide complexes. The difference in gold leaching efficiency between using raffinate and fresh water was negligible.

Synthesis, characterization and antimicrobial activity of dextran sulphate stabilized silver nanoparticles

Science.gov (United States)

Cakić, Milorad; Glišić, Slobodan; Nikolić, Goran; Nikolić, Goran M.; Cakić, Katarina; Cvetinov, Miroslav

2016-04-01

Dextran sulphate stabilized silver nanoparticles (AgNPs - DS) were synthesized from aqueous solution of silver nitrate (AgNO3) and dextran sulphate sodium salt (DS). The characterization of AgNPs - DS was performed by ultraviolet-visible spectroscopy (UV-VIS), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR) and antimicrobial activity. The formation of AgNPs - DS was monitored by colour changes of the reaction mixture from yellowish to brown and by measuring the surface plasmon resonance absorption peak in UV-VIS spectra at 420 nm. The SEM analysis was used for size and shape determination of AgNPs - DS. The presence of elemental silver and its crystalline structure in AgNPs - DS were confirmed by EDX and XRD analyses. The possible functional groups of DS responsible for the reduction and stabilization of AgNPs were determinated by FTIR spectroscopy. The AgNPs - DS showed strong antibacterial activity against Staphylococcus aureus ATCC 25923, Bacillus cereus ATCC 11778, Bacillus luteus in haus strain, Bacillus subtilis ATTC 6633, Listeria monocytogenes ATCC 15313, Escherichia coli ATTC 25922, Pseudomonas aeruginosa ATTC 27853, Klebsiella pneumoniae ATTC 700603, Proteus vulgaris ATTC 8427, and antifungal activity against Candida albicans ATTC 2091.

Development and characterization of mucoadhesive buccal patches of salbutamol sulphate.

Science.gov (United States)

Patel, Rajesh Singh; Poddar, S S

2009-01-01

Mucoadhesive patch releasing the drug in the oral cavity at predetermined rate may present distinct advantages over traditional dosage forms such as tablets, gels and solutions. The present study was concerned with the preparation and evaluation of mucoadhesive buccal patches for the controlled systemic delivery of Salbutamol sulphate to avoid first pass hepatic metabolism. The developed patches were evaluated for the physicochemical, mechanical and drug release characteristics. The patches showed desired mechanical and physicochemical properties to withstand environment of oral cavity. The in-vitro release study showed that patches could deliver drug to the oral mucosa for a period of 7 h. the patches exhibited adequate stability when tested under accelerated conditions.

Magnesium sulphate and other anticonvulsants for women with pre-eclampsia.

Science.gov (United States)

Duley, Lelia; Gülmezoglu, A Metin; Henderson-Smart, David J; Chou, Doris

2010-11-10

Eclampsia, the occurrence of a seizure (fit) in association with pre-eclampsia, is rare but potentially life-threatening. Magnesium sulphate is the drug of choice for treating eclampsia. This review assesses its use for preventing eclampsia. To assess the effects of magnesium sulphate, and other anticonvulsants, for prevention of eclampsia. We searched the Cochrane Pregnancy and Childbirth Group's Trials Register (4 June 2010), and the Cochrane Central Register of Controlled Trials Register (The Cochrane Library 2010, Issue 3). Randomised trials comparing anticonvulsants with placebo or no anticonvulsant, or comparisons of different drugs, for pre-eclampsia. Two authors assessed trial quality and extracted data independently. We included 15 trials. Six (11,444 women) compared magnesium sulphate with placebo or no anticonvulsant: magnesium sulphate more than a halved the risk of eclampsia (risk ratio (RR) 0.41, 95% confidence interval (CI) 0.29 to 0.58; number needed to treat for an additional beneficial outcome (NNTB) 100, 95% CI 50 to 100), with a non-significant reduction in maternal death (RR 0.54, 95% CI 0.26 to 1.10) but no clear difference in serious maternal morbidity (RR 1.08, 95% CI 0.89 to 1.32). It reduced the risk of placental abruption (RR 0.64, 95% CI 0.50 to 0.83; NNTB 100, 95% CI 50 to 1000), and increased caesarean section (RR 1.05, 95% CI 1.01 to 1.10). There was no clear difference in stillbirth or neonatal death (RR 1.04, 95% CI 0.93 to 1.15). Side effects, primarily flushing, were more common with magnesium sulphate (24% versus 5%; RR 5.26, 95% CI 4.59 to 6.03; number need to treat for an additional harmful outcome (NNTH) 6, 95% CI 5 to 6).Follow-up was reported by one trial comparing magnesium sulphate with placebo: for 3375 women there was no clear difference in death (RR 1.79, 95% CI 0.71 to 4.53) or morbidity potentially related to pre-eclampsia (RR 0.84, 95% CI 0.55 to 1.26) (median follow-up 26 months); for 3283 children exposed in utero

Method for aqueous gold thiosulfate extraction using copper-cyanide pretreated carbon adsorption

Science.gov (United States)

Young, Courtney; Melashvili, Mariam; Gow, Nicholas V

2013-08-06

A gold thiosulfate leaching process uses carbon to remove gold from the leach liquor. The activated carbon is pretreated with copper cyanide. A copper (on the carbon) to gold (in solution) ratio of at least 1.5 optimizes gold recovery from solution. To recover the gold from the carbon, conventional elution technology works but is dependent on the copper to gold ratio on the carbon.

Analysis of the hygroscopic and volatile properties of ammonium sulphate seeded and unseeded SOA particles

Directory of Open Access Journals (Sweden)

N. K. Meyer

2009-01-01

Full Text Available The volatile and hygroscopic properties of ammonium sulphate seeded and unseeded secondary organic aerosol (SOA derived from the photo-oxidation of atmospherically relevant concentrations of α-pinene were studied. The seed particles were electrospray generated ammonium sulphate ((NH4₂SO₄ having diameters of approximately 33 nm with a quasi-mono-disperse size distribution (geometric standard deviation σ_g=1.3. The volatile and hygroscopic properties of both seeded and unseeded SOA were simultaneously measured with a VH-TDMA (volatility – hygroscopicity tandem differential mobility analyzer. VH-TDMA measurements of unseeded SOA show a decrease in the hygroscopic growth (HGF factor for increased volatilisation temperatures such that the more volatile compounds appear to be more hygroscopic. This is opposite to the expected preferential evaporation of more volatile but less hygroscopic material, but could also be due to enhanced oligomerisation occurring at the higher temperature in the thermodenuder. In addition, HGF measurements of seeded SOA were measured as a function of time at two relative humidities, below (RH 75% and above (RH 85% the deliquescence relative humidity (DRH of the pure ammonium sulphate seeds. As these measurements were conducted during the onset phase of photo-oxidation, during particle growth, they enabled us to find the dependence of the HGF as a function of the volume fraction of the SOA coating. HGF's measured at RH of 85% showed a continuous decrease as the SOA coating thickness increased. The measured growth factors show good agreements with ZSR predictions indicating that, at these RH values, there are only minor solute-solute interactions. At 75% RH, as the SOA fraction increased, a rapid increase in the HGF was observed indicating that an increasing fraction of the (NH₄₂SO₄ is subject to a phase transition, going into solution, with an

Performance of cement solidification with barium for high activity liquid waste including sulphate

International Nuclear Information System (INIS)

Waki, Toshikazu; Yamada, Motoyuki; Horikawa, Yoshihiko; Kaneko, Masaaki; Saso, Michitaka; Haruguchi, Yoshiko; Yamashita, Yu; Sakai, Hitoshi

2009-01-01

The target liquid waste to be solidified is generated from PWR primary loop spent resin treatment with sulphate acid, so, its main constituent is sodium sulphate and the activity of this liquid is relatively high. Waste form of this liquid waste is considered to be a candidate for the subsurface disposal. The disposed waste including sulphate is anticipated to rise a concentration of sulphate ion in the ground water around the disposal facility and it may cause degradation of materials such as cement and bentonite layer and comprise the disposal facility. There could be two approaches to avoid this problem, the strong design of the disposal facility and the minimization of sulphaste ion migration from the solidified waste. In this study, the latter approach was examined. In order to keep the low concentration of sulphate ion in the ground water, it is effective to make barium sulphate by adding barium compound into the liquid waste in solidification. However, adding equivalent amount of barium compound with sulphate ion causes difficulty of mixing, because production of barium sulphate causes high viscosity. In this study, mixing condition after and before adding cement into the liquid waste was estimated. The mixing condition was set with consideration to keep anion concentration low in the ground water and of mixing easily enough in practical operation. Long term leaching behavior of the simulated solidified waste was also analyzed by PHREEQC. And the concentration of the constitution affected to the disposal facility was estimated be low enough in the ground water. (author)

Anti-corrosion film formed on HAl77-2 copper alloy surface by aliphatic polyamine in 3 wt.% NaCl solution

Energy Technology Data Exchange (ETDEWEB)

Yu, Yinzhe; Yang, Dong; Zhang, Daquan, E-mail: zhdq@sh163.net; Wang, Yizhen; Gao, Lixin

2017-01-15

Highlights: • Properties of ADDD meet environment-friendly requirements. • ADDD’s inhibition efficiency is better than BTA at the low concentration. • ADDD adsorbs on the copper alloy surface by via the N atom in its amino group using flat mode. - Abstract: The corrosion inhibition of a polyamine compound, N-(4-amino-2, 3-dimethylbutyl)-2, 3-dimethylbutane-1, 4-diamine (ADDD), was investigated for HAl77-2 copper alloy in 3 wt.% NaCl solution. Electrochemical measurements, scanning electron microscopy (SEM), atomic force microscope (AFM) and Fourier transform infrared spectroscopy (FT-IR) techniques were employed for this research. The results show that ADDD strongly suppresses the corrosion of HAl77-2 alloy. The inhibition efficiency of ADDD is 98.6% at 0.5 mM, which is better than benzotriazole (BTAH) at the same concentration. Polarization curves indicate that ADDD is an anodic type inhibitor. Surface analysis suggests that a protective film is formed via the interaction of ADDD and copper. FT-IR reveals that the inhibition mechanism of ADDD is dominated by chemisorption onto the copper alloy surface to form an inhibition film. Furthermore, quantum chemical calculation and molecular dynamics (MD) simulations methods show that ADDD adsorbs on HAl77-2 surface via amino group in its molecule.

Flexible substrate compatible solution processed P-N heterojunction diodes with indium-gallium-zinc oxide and copper oxide

Energy Technology Data Exchange (ETDEWEB)

Choudhary, Ishan; Deepak, E-mail: saboo@iitk.ac.in

2017-04-15

Highlights: • Both n and p-type semiconductors are solution processed. • Temperature compatibility with flexible substrates such as polyimide. • Compatibility of p-type film (CuO) on n-type film (IZO). • Diode with rectification ratio of 10{sup 4} and operating voltage <1.5 V. • Construction of band alignment using XPS. - Abstract: Printed electronics on flexible substrates requires low temperature and solution processed active inks. With n-type indium-gallium-zinc oxide (IGZO) based electronics maturing for thin film transistor (TFT), we here demonstrate its heterojunction diode with p-copper oxide, prepared by sol-gel method and processed at temperatures compatible with polyimide substrates. The phase obtained for copper oxide is CuO. When coated on n-type oxide, it is prone to develop morphological features, which are minimized by annealing treatment. Diodes of p-CuO films with IGZO are of poor quality due to its high resistivity while, conducting indium-zinc oxide (IZO) films yielded good diode with rectification ratio of 10{sup 4} and operating voltage <1.5 V. A detailed measurement at the interface by X-ray photoelectron spectroscopy and optical absorption ascertained the band alignment to be of staggered type. Consistently, the current in the diode is established to be due to electrons tunnelling from n-IZO to p-CuO.

Activity and deactivation of sulphated TiO2- and ZrO2-based V, Cu, and Fe oxide catalysts for NO abatement in alkali containing flue gases

DEFF Research Database (Denmark)

Kustov, Arkadii; Rasmussen, Søren Birk; Fehrmann, Rasmus

2007-01-01

Vanadia, copper and iron oxide catalysts supported on conventional TiO2, ZrO2, and sulphated-TiO2 and ZrO2 have been prepared. These catalysts were characterized by elemental analysis, N-2-BET, XRD, and NH3-TPD methods. The influence of potassium oxide additives on the acidity and activity...... of the catalysts with potassium leads to a considerable decrease of their catalytic activity. In the case of the traditional carriers (TiO2, ZrO2), the poisoning of the catalyst with small amounts of potassium oxide (K/metal ratio...

Seeding of silicon by copper ion implantation for selective electroless copper plating

Energy Technology Data Exchange (ETDEWEB)

Bhansali, S.; Sood, D.K.; Zmood, R.B. [Microelectronic and Materials Technology Centre, Royal Melbourne Institute of Technolgy, Melbourne, VIC (Australia)

1993-12-31

We report on the successful use of copper(self) ion implantation into silicon to seed the electroless plating of copper on silicon (100) surfaces. Copper ions have been implanted to doses of 5E14-6.4E16 ions/cm{sup 2} using a MEEVA ion implanter at extraction voltage of 40kV. Dose was varied in fine steps to determine the threshold dose of 2E15 Cu ions/cm{sup 2} for `seed` formation of copper films on silicon using a commercial electroless plating solution. Plated films were studied with Rutherford backscattering spectrometry, scanning electron microscopy, EDX and profilometry . The adhesion of films was measured by `scotch tape test`. The adhesion was found to improve with increasing dose. However thicker films exhibited rather poor adhesion and high internal stress. SEM results show that the films grow first as isolated islands which become larger and eventually impinge into a continuous film as the plating time is increased. (authors). 5 refs., 1 tab., 3 figs.

Seeding of silicon by copper ion implantation for selective electroless copper plating

Energy Technology Data Exchange (ETDEWEB)

Bhansali, S; Sood, D K; Zmood, R B [Microelectronic and Materials Technology Centre, Royal Melbourne Institute of Technolgy, Melbourne, VIC (Australia)

1994-12-31

We report on the successful use of copper(self) ion implantation into silicon to seed the electroless plating of copper on silicon (100) surfaces. Copper ions have been implanted to doses of 5E14-6.4E16 ions/cm{sup 2} using a MEEVA ion implanter at extraction voltage of 40kV. Dose was varied in fine steps to determine the threshold dose of 2E15 Cu ions/cm{sup 2} for `seed` formation of copper films on silicon using a commercial electroless plating solution. Plated films were studied with Rutherford backscattering spectrometry, scanning electron microscopy, EDX and profilometry . The adhesion of films was measured by `scotch tape test`. The adhesion was found to improve with increasing dose. However thicker films exhibited rather poor adhesion and high internal stress. SEM results show that the films grow first as isolated islands which become larger and eventually impinge into a continuous film as the plating time is increased. (authors). 5 refs., 1 tab., 3 figs.

Seeding of silicon by copper ion implantation for selective electroless copper plating

International Nuclear Information System (INIS)

Bhansali, S.; Sood, D.K.; Zmood, R.B.

1993-01-01

We report on the successful use of copper(self) ion implantation into silicon to seed the electroless plating of copper on silicon (100) surfaces. Copper ions have been implanted to doses of 5E14-6.4E16 ions/cm 2 using a MEEVA ion implanter at extraction voltage of 40kV. Dose was varied in fine steps to determine the threshold dose of 2E15 Cu ions/cm 2 for 'seed' formation of copper films on silicon using a commercial electroless plating solution. Plated films were studied with Rutherford backscattering spectrometry, scanning electron microscopy, EDX and profilometry . The adhesion of films was measured by 'scotch tape test'. The adhesion was found to improve with increasing dose. However thicker films exhibited rather poor adhesion and high internal stress. SEM results show that the films grow first as isolated islands which become larger and eventually impinge into a continuous film as the plating time is increased. (authors). 5 refs., 1 tab., 3 figs

Stress corrosion cracking of Inconel 600 in aqueous solutions at elevated temperature. Pt. II. Effects of chloride and sulphate ions on the electrochemical behaviour of Inconel 600

International Nuclear Information System (INIS)

Ashour, E.A.; Schneider, F.; Mummert, K.

1997-01-01

For pt.I see ibid., p.151-6, 1997. The influencing effects of temperature, potential and electrolyte composition on the electrochemical behaviour of Inconel 600 in aqueous solutions are presented. Considering these effects the connection between the data have been obtained from chemo-mechanical fracture investigation on CT-samples in Part I of this paper and pitting corrosion are discussed. The results have shown that chloride ions depassivate the surfaces of cracks locally and hinder the formation of a new protective oxide layer on the fracture surfaces. Furthermore, chloride promotes the dissolution of metal and initiates the cracking, respectively. The resulting crevice corrosion promotes an increase of hydrogen absorption by the metal. The increase of the hydrogen content of the metal influences the mechanical fracture behaviour. Contrary, sulphate ions inhibit the initiation of corrosion mainly due to a hinderance of chloride ions adsorption on active sites of the fracture surfaces. The initiation of localized corrosion in the crevice region may be stimulated by chromate ions formed by oxidation of chromium from the oxide layer or the base metal in oxygen containing solutions. (orig.)

Effect of temperature on sulphate reduction, growth rate and growth yield in five psychrophilic sulphate-reducing bacteria from Arctic sediments

DEFF Research Database (Denmark)

Knoblauch, C.; Jørgensen, BB

1999-01-01

Five psychrophilic sulphate-reducing bacteria (strains ASv26, LSv21, PSv29, LSv54 and LSv514) isolated from Arctic sediments were examined for their adaptation to permanently low temperatures, All strains grew at -1.8 degrees C, the freezing point of sea water, but their optimum temperature...... and T(opt). For strains LSv21 and LSv514, however, growth yields were highest at the lowest temperatures, around 0 degrees C. The results indicate that psychrophilic sulphate-reducing bacteria are specially adapted to permanently low temperatures by high relative growth rates and high growth yields...... at in site conditions....

Estimating global copper demand until 2100 with regression and stock dynamics

NARCIS (Netherlands)

Schipper, Branco W.; Lin, Hsiu Chuan; Meloni, Marco A.; Wansleeben, Kjell; Heijungs, Reinout; van der Voet, Ester

2018-01-01

Future global copper demand is expected to keep rising due to copper's indispensable role in modern technologies. Unfortunately, increasing copper extraction and decreasing ore grades intensify energy use and generate higher environmental impact. A potential solution would be reaching a circular

Complete sulphate removal from neutralised acidic mine drainage with barium carbonate

CSIR Research Space (South Africa)

Swanepoel, H

2012-03-01

Full Text Available -barium-calcium) Desalination process which uses barium salts to further reduce the sulphate concentration to acceptable levels with the added advantage that sulphate removal can be controlled due to the low solubility of BaSO4. This paper reports on the results...

Recovery of Copper from Copper Slag by Hydrometallurgy Method, from Iraqi Factories Waste

Directory of Open Access Journals (Sweden)

Bahaa Sami Mahdi

2018-05-01

Full Text Available   In this research, the recovery of copper from copper slag is investigated using hydrometallurgy method. Slag samples were taken from Al-Shaheed State Company. The results of the chemical analysis showed that the slag contained 11.4% of copper. The recovery process included two stages; the first stage is leaching using diluted sulfuric acid. The most important variables that effect on the leaching process was studied, such as acid concentration, hydrogen peroxide adding, particle size, liquid to solid, stirring speed and leaching time by changing the condition and the stabilizing of other factors at room temperature.               The second stage is precipitation of copper from leaching solution by zinc powder with different weights and times, at room temperature and 1.5 PH value. The results of the first stage manifested that about 99.7% of the copper have been dissolved at the following operational conditions: 50% acid concentration, 5 ml hydrogen peroxide adding, particle size (-75+53 micron, 1:10 liquid to solid, 500 rpm stirring speed and 25 min of leaching time. The highest percentage of copper precipitation in the second stage was 99.8% when added 3gm zinc powder at 20 min. The XRD result revealed that the predominant phase was pure copper. The results of EDS exhibited that a few percentage of oxygen appeared with copper powder. The final of copper recovery ratio was 99.3% with 99.2% purity.

On the stabilization of NbV-solutions by ZrIV and HfIV

International Nuclear Information System (INIS)

Soerensen, E.; Bjerre, A.B.

1987-11-01

Niobium cannot be separated from zirconium or hafnium when these elements occur together in solution with common anions such as Cl- and SO 4 --. This is ascribed to the copolymerisation of Nb v and the hydrolyzed ionic species of Zr IV v and Hf IV by which the colloidal particles are masked as Zr- and Hf-compounds. In HCl the particles are positively charged as opposed to when they are in sulphate solution where the Zr- and Hf- sulphate complexes confer a negative charge. The two cases are considered separately. (author)

Iontophoresis of minoxidil sulphate loaded microparticles, a strategy for follicular drug targeting?

Science.gov (United States)

Gelfuso, Guilherme M; Barros, M Angélica de Oliveira; Delgado-Charro, M Begoña; Guy, Richard H; Lopez, Renata F V

2015-10-01

The feasibility of targeting drugs to hair follicles by a combination of microencapsulation and iontophoresis has been evaluated. Minoxidil sulphate (MXS), which is used in the treatment of alopecia, was selected as a relevant drug with respect to follicular penetration. The skin permeation and disposition of MXS encapsulated in chitosan microparticles (MXS-MP) was evaluated in vitro after passive and iontophoretic delivery. Uptake of MXS was quantified at different exposure times in the stratum corneum (SC) and hair follicles. Microencapsulation resulted in increased (6-fold) drug accumulation in the hair follicles relative to delivery from a simple MXS solution. Application of iontophoresis enhanced follicular delivery for both the solution and the microparticle formulations. It appears, therefore, that microencapsulation and iontophoresis can act synergistically to enhance topical drug targeting to hair follicles. Copyright © 2015 Elsevier B.V. All rights reserved.

Method For Creating Corrosion Resistant Surface On An Aluminum Copper Alloy

Science.gov (United States)

Mansfeld, Florian B.; Wang, You; Lin, Simon H.

1997-06-03

A method for treating the surface of aluminum alloys hang a relatively high copper content is provided which includes the steps of removing substantially all of the copper from the surface, contacting the surface with a first solution containing cerium, electrically charging the surface while contacting the surface in an aqueous molybdate solution, and contacting the surface with a second solution containing cerium. The copper is substantially removed from the surface in the first step either by (i) contacting the surface with an acidic chromate solution or by (ii) contacting the surface with an acidic nitrate solution while subjecting the surface to an electric potential. The corrosion-resistant surface resulting from the invention is excellent, consistent and uniform throughout the surface. Surfaces treated by the invention may often be certified for use in salt-water services.

Stream plant chemistry as indicator of acid sulphate soils in Sweden

Directory of Open Access Journals (Sweden)

K. LAX

2008-12-01

Full Text Available Results from the biogeochemical mapping (roots of aquatic plants and Fontinalis antipyretica conducted by the Geological Survey of Sweden (SGU reflects the metal load of surface waters draining acid sulphate (AS soils in Sweden. In this study, results from the biogeochemical, soil geochemical and Quaternary mapping programmes at SGU were used to investigate the impact of fine-grained deposits hosting AS soils on stream water trace element chemistry in two separate areas. In the area around Lake Mälaren, postglacial sediments contain the highest levels of most trace elements studied. Owing to the low pH of AS soils and subsequent leaching, levels of nickel (Ni, cobalt (Co, copper (Cu, sulphur (S, yttrium (Y, uranium (U, tungsten (W, and molybdenum (Mo were significantly elevated in aquatic roots. Levels were lower in the Skellefteå area, which may be explained by lower concentrations in source deposits. Concentrations of arsenic (As and lead (Pb were normal or impoverished in biogeochemical samples from postglacial, finegrained sediment areas. Maps based on ratios (Ni:Pb or Y:Pb in biogeochemical samples can, together with results from Quaternary mapping, be used to predict areas with AS soils in Sweden.;

Development of melt compositions for sulphate bearing high level waste

International Nuclear Information System (INIS)

Jahagirdar, P.B.; Wattal, P.K.

1997-09-01

The report deals with the development and characterization of vitreous matrices for sulphate bearing high level waste. Studies were conducted in sodium borosilicate and lead borosilicate systems with the introduction of CaO, BaO, MgO etc. Lead borosilicate system was found to be compatible with sulphate bearing high level wastes. Detailed product evaluation carried on selected formulations is also described. (author)

Microbial leaching of low grade copper ores

International Nuclear Information System (INIS)

Rauf, A.; Ashfaq, M.

1991-01-01

Biotechnology is regarded as one of the most promising and revolutionary solution to various problems which are generally faced in the extraction of metals from their ores such as high energy, capital costs and environmental pollution. The paper deals with the study of low grade copper ores for their beneficiation and extraction of copper. The ores used were chalcopyrite and oxidized copper ores. Microorganisms play a vital role in the solubilization of valuable contents from ores such as copper and other metals. Studies have been conducted on the indigenous copper ores by using thiobacillus ferro oxidans and thiobacillus thio oxidans. For comparison purpose some experiments have also been conducted by chemical leaching. The results of bacterial leaching are encouraging. (author)

SOLUBILITIES AND PHYSICAL PROPERTIES OF SATURATED SOLUTIONS IN THE COPPER SULFATE + SULFURIC ACID + SEAWATER SYSTEM AT DIFFERENT TEMPERATURES

OpenAIRE

Justel, F. J.; Claros, M.; Taboada, M. E.

2015-01-01

Abstract In Chile, the most important economic activity is mining, concentrated in the north of the country. This is a desert region with limited water resources; therefore, the mining sector requires research and identification of alternative sources of water. One alternative is seawater, which can be a substitute of the limited fresh water resources in the region. This work determines the influence of seawater on the solid-liquid equilibrium for acid solutions of copper sulfate at different...

Inhibiting effects of imidazole on copper corrosion in 1 M HNO3 solution

International Nuclear Information System (INIS)

Lee, Woo-Jin

2003-01-01

The present work deals with the inhibiting effects of imidazole on the pure copper (Cu) corrosion in 1 M HNO 3 solution analysing potentiodynamic polarisation curves, potentiostatic anodic current transient, AC impedance spectra and X-ray photoelectron spectra (XPS). By adding imidazole to HNO 3 solution, the polarisation curves showed decrease in the corrosion current and the cathodic current, suggesting that imidazole acts as an effective cathodic inhibitor to Cu corrosion. From the measured anodic current transients, it is inferred that the protective Cu-imidazole complex film is simultaneously formed with the Cu oxide in the presence of imidazole during the early stage of the anodic polarisation. Analysis of the AC impedance spectra revealed that the values of the charge transfer resistance R ct obtained in imidazole-containing HNO 3 solution were greater than that value in imidazole-free one and at the same time steadily increased with immersion time to the constant value. Contrarily, the capacitance value was abruptly lowered from the double layer capacitance C dl to the complex film capacitance C cf in the progress of immersion time. Furthermore, the Warburg coefficient σ value for the ion diffusion through the complex film was observed to increase with immersion time. This means that the Cu(N-OH) complex film becomes thicker during immersion in the HNO 3 solution with imidazole through the inward growth of the N-rich outer layer to the O-rich inner layer, as well validated by XPS. Based upon the experimental results, it is suggested that the Cu corrosion in 1 M HNO 3 solution is efficiently inhibited with the addition of imidazole by retarding both the charge transfer on cathodic sites of the Cu surface in the early stage of immersion time and the subsequent ion diffusion through the steadily growing complex film

A Study on Carbon Fiber (Long Fiber) Reinforced Copper Matrix Composite

Science.gov (United States)

1990-03-30

complex may be coke phosphate, 7 EDTA, NTA, tartrate , citrate, etc. added by proper amount of op series activating agent. It has the following property...significantly improved. Discharge with large current is proper in order to reduce the time of electrodeposition, so acidity cupric sulphate solution is

Differential inhibition of polymorphonuclear leukocyte recruitment in vivo by dextran sulphate and fucoidan

Directory of Open Access Journals (Sweden)

N. Van Osselaer

1996-01-01

Full Text Available The selectin-mediated rolling of leukocytes along the endothelial cells is a prerequisite step followed by firm adhesion and extravasation into the inflamed tissue. This initial contact can be suppressed by sulphated polysaccharides. We have studied the effect of sulphated polysaccharides on the ultimate polymorphonuclear leukocyte (PMN recruitment and plasma leakage in rabbit skin in response to intradermal injection of various inflammatory mediators. PMN infiltration evoked by various PMN chemoattractants (FMLP, C5a desArg, LTB4 and IL-8 was significantly inhibited after intravenous injection of dextran sulphate (25 mg/kg, heparin (2 × 90 mg/kg or fucoidan (1 mg/kg. PMN-dependent plasma leakage was equally well reduced by the different sulphated polymers. Vascular permeability induced by histamine or thrombin acting via a PMN-independent mechanism was not reduced. Fucoidan was the only polysaccharide able to suppress IL-1-induced PMN infiltration for 60–70%. Local administration of dextran sulphate had no effect on PMN-dependent plasma leakage. Differential inhibition of PMN recruitment was determined after injection of dextran sulphate or fucoidan depending on the type of insult. Therefore, these results suggest that different adhesion pathways are utilized during PMN recruitment in vivo in response to chemoattractants and IL-1.

Absolute calibration system of neutron sources by the manganese sulphate bath

International Nuclear Information System (INIS)

Fonseca, E.S. da; Sachett, I.A.

1990-01-01

The calibration system consists of deep the neutron source, protected by plastic container, at the center of spherical polietilene tank, in a concentrated solution of manganese sulphate. The neutrons emitted by the source are moderated and when reach the termal energy are catched by manganese atoms activating the solution. After the saturation activity has been reached the source is removed and one scintilation detector (NaI(Tl) 3' x 3') is put in the same place to follow the decay activity. The gama couting rate (845 KeV 54 Mn photopeak), after the corrections is used to estimate the saturation activity, and calculate the neutron source emission rate. These calculations are executed by one computer program. The uncertainties in the final value of emission rate are about 2.5 - 3.0 % to AmBe sources in the 1.11 x 10 10 Bq (0,3 Ci) - 3.7 x 10 11 Bq (10 Ci) range. (author) [pt

Corrosivity Index Copper and Steel at Two Locations in Villahermosa, Tabasco

Directory of Open Access Journals (Sweden)

Tejero-Rivas María Candelaria

2015-03-01

Full Text Available This paper presents a study of the atmospheric corrosion of copper and carbon steel made ​​in two environments Villahermosa, Tabasco for six months. The test site of the industrial zone started Villahermosa Institute of Technology (ITVH and rural-urban site at the Technological University of Tabasco (UTTAB. Aluminum in combination with a screw carbon steel provided the index marine corrosivity (MA, the brass screw gives the index of industrial corrosivity (IA; wire method of screw according to ASTM G116-93 was used and the plastic screw nylon gives the rate of rural-urban corrosivity (RUA. The determination of air pollutants (sulfur dioxide and chlorides, was with the methods of wet candle and sulfation plates according to ISO 9225. Morphology studies were performed on the corrosion products formed on the specimens screw, using scanning electron microscopy coupled with energy dispersive. The corrosion products that formed on the surface of copper and carbon steel, having a bulb-shaped morphology characteristic of the addition of soluble salts, particularly sulphates and chlorides, were identified in the two stations.

Influence on ammonium-sulphate fertilizer on P-uptake by upland rice

International Nuclear Information System (INIS)

Abdullah, N; Mitrosuhardjo, M.M.

1988-01-01

A greenhouse experiment to study the influence of ammonium -sulphate fertilizer on P-uptake by Atomita I/1 rice variety on latosol soil of Pasar Jumat has been conducted. Factorial experiment consisting of eight treatments was arrange in a fully randomized design. Each treatment was replicated three times. The rate of ammonium sulphate fertilizer was equivalent to 0, 30, 60, and 90 kg N/ha, and TSP at the rate of 90 and 180 kg P/ha. Ammonium sulphate fertilizer with 2% atom 15-N and TSP with specific activity of 0.2 mCi/g P2O5 were used in the experiment. The plant was harvested 70 days after planting, It was turned out that ammonium sulphate fertilizer gave a highly significant difference (p=<0.01) of dry weight of plant. The rate of TSP did not effect significantly on plant dry weight. Ammonium sulphate fertilizer gave highly significant difference on P-uptake. Fertilizer use efficiency was in the range of 3.88 - 6.60% for 90 kg P and 2.51 - 4.46% for 180 kg P. Fertilizer-N uptake was significantly increased (p=<0.05) with the increase of N rate. Rate of fertilizer-N use efficiency was in the range of 47-60% of the applied fertilizer. (authors). 4 refs, 9 tabs

Influence of the Interaction between Sphalerite and Pyrite on the Copper Activation of Sphalerite

Directory of Open Access Journals (Sweden)

Bo Yang

2018-01-01

Full Text Available In this paper, the effect of pyrite on the activation of sphalerite was investigated by micro-flotation, copper adsorption experiments, X-ray photoelectron spectroscopy (XPS, and electrochemical measurement. The micro-flotation test results showed that the recovery and flotation rate of sphalerite with copper sulphate as activator and butyl xanthate as collector were significantly decreased with the increasing content of pyrite in pulp. Cu2+ adsorption results indicated that the adsorption of Cu2+ on the sphalerite surface were decreased when pyrite was present in the pulp. XPS surface analysis demonstrated that the proportion of Cu+ species increased in the activation products on the sphalerite surface, but the total atomic concentration of Cu atom was decreased. Linear voltammetry measurement suggested that the current density of Cu+ species oxidizing to Cu2+ species was increased when sphalerite was electrically contacted with pyrite, which confirmed the increased proportion of Cu+ species on Cu-activation sphalerite surface when contacting with pyrite. These results indicated that there is not only a competitive adsorption for cupric ions (Cu2+, but the galvanic interaction between sphalerite and pyrite also has a significant influence on the copper activation of sphalerite.

Tyrosine sulphation is not required for microvillar expression of intestinal aminopeptidase N

DEFF Research Database (Denmark)

Danielsen, E M

1988-01-01

incorporation of [35S]sulphate into aminopeptidase N and other major microvillar hydrolases by 70-85% compared with controls, indicating an inhibition of their post-translational tyrosine sulphation. In labelling experiments with [35S]methionine from 0.5 to 5 h, DCNP was tested for its possible influence...... on synthesis, processing and microvillar expression of aminopeptidase N, but no effect on any of these parameters could be detected. It can therefore be concluded that tyrosine sulphation is not required (for instance as a sorting signal) for the targeting of newly synthesized enzymes to the microvillar...

The influence of silicate and sulphate anions on the anodic corrosion and the transpassivity of iron and silicon-rich steel in concentrated KOH solution

International Nuclear Information System (INIS)

Čekerevac, Milan; Simičić, Miloš; Bujanović, Ljiljana Nikolić; Popović, Negica

2012-01-01

Highlights: ► Anodic behaviour of Fe and steel in 10 M KOH with sulphate and silicate is examined. ► X-ray diffraction confirmed the formation of Fe 3 (Si 1.32 Fe 0.68 )O 5 (OH) 4 in anodic layer. ► X-ray diffraction confirmed the formation of Ba(Fe, S)O 4 at anodic oxidation. - Abstract: The effect of sulphate and silicate addition in a 10 M KOH electrolyte on the anodic corrosion and transpassivity of iron and steel rich in silicon are explored by cyclic and linear sweep voltammetry. Formation of ferrate(VI) in the iron transpassivity region is noticed in all explored electrolytes. The electrochemical sulphato- and silico-ferrate(VI) formation is discussed as a possible result of Fe 3 III (Si 1.32 Fe 0.68 )O 5 (OH) 4 and [Fe(II) 4 Fe(III) 2 (OH) 12 ]SO 4 oxidation in the 10 M KOH electrolytes with silicate and sulphate, respectively. The presence of Fe 3 (Si 1.32 Fe 0.68 )O 5 (OH) 4 in the anodic layer of silicon steel and the crystal structure of electrochemically synthesised Ba(Fe, S)O 4 have been revealed by XRD.

ELECTROCHEMICAL BEHAVIOR OF POLYCRYSTALLINE COPPER DURING THE ADSORPTION OF CO ABSTRACT

Directory of Open Access Journals (Sweden)

J. Salimon

2017-12-01

Full Text Available The electrochemical properties of electrode copper in carbon monoxide-saturated phosphate buffered solution were investigated. The electrochemistry of copper surface was sufficiently changed after the supporting electrolyte solution was saturated with CO. The hydrogen evolution region was depressed and shifted cathodically due to the adsorption process of CO on the copper surface in a linear or terminally bonded manner, Cu-CO . The oxidation and the reduction peaks of copper were significantly changed with two couple of redox peaks. This is due to the subsequent formation and the corresponding reduction of copper(I and the copper carbon monoxides species. Further changed in electrochemical properties occurred when the electrode surface was polarized at high cathodic potential (-1.4 V for a period of time (15 min. The hydrogen evolution region was further depressed due to the adsorption of CO process in multiple bonding sites as adsorbed bridge bonded CO, Cu-CO B L that occurred predominantly.

Oxygen isotopic composition of sulphates from some mineral waters and mine waters in western Bohemia

International Nuclear Information System (INIS)

Smejkal, V.

1979-01-01

Two main genetic types of sulphate can be distinguished according to the delta 18 O(SO 4 2- ) measurements in sulphate-rich mineral and mine waters of western Bohemia - sulphates in descending mine waters and in weathered outcrops of graphitic pyrite slates from areas outside Tertiary basins, which originated in recent time by the oxidation of sulphides in the presence of atmospheric oxygen, have delta 18 O values from -2.1 to -6.1 per mille SMOW; and sulphates from springs of mineral waters of the renowned spas of Karlovy Vary, Frantiskovy Lazne and Marianske Lazne show distinctly heavier delta 18 O values - from +4.0 to +6.4 per mille, with maximum of values between +5.0 and +6.0 per mille. Similar delta 18 O values have been established in thenardites and in gypsum in Miocene claystones and in sulphates of some mine waters in the nearby Tertiary Cheb and Sokolov Basins. The presented results indicate that sulphates in mineral waters of the Karlovy Vary type originate mainly by leaching of Miocene sulphates and not by present-day oxidation of sulphidic sulphur. (author)

Possibilities of Sulphate Elimination from Mine Water

Directory of Open Access Journals (Sweden)

Heviánková Silvie

2004-12-01

Full Text Available The issue of „acid water“ (or AMD is well known in the world for some centuries. In the Eastern Slovakia, the most acid surface water occurs in the area of old mine Smolník, which is closed and submerged for 15 years. The submitted contribution deals with the sulphate-elimination from this locality. Recently, several methods of sulphate-elimination from the mine water are applied. The best-known methods are biological, physical-chemical and chemical precipitation. The method described in this contribution consists of chemical precipitation by sodium aluminate and calcium hydrate. Under application of this method very interesting results were obtained. The amount of SO42- anions decreased to almost zero-value, using optimal doses of the chemical reagents.

Grain boundary corrosion of copper canister weld material

International Nuclear Information System (INIS)

Gubner, Rolf; Andersson, Urban; Linder, Mats; Nazarov, Andrej; Taxen, Claes

2006-01-01

The proposed design for a final repository for spent fuel and other long-lived residues in Sweden is based on the multi-barrier principle. The waste will be encapsulated in sealed cylindrical canisters, which will then be placed in granite bedrock and surrounded by compacted bentonite clay. The canister design is based on a thick cast inner container fitted inside a corrosion-resistant copper canister. During fabrication of the outer copper canisters there will be some unavoidable grain growth in the welded areas. As grains grow, they will tend to concentrate impurities within the copper at the new grain boundaries. The work described in this report was undertaken to determine whether there is any possibility of enhanced corrosion at grain boundaries within the copper canister, based on the recommendations of the report SKB-TR--01-09 (INIS ref. 32025363). Grain boundary corrosion of copper is not expected to be a problem for the copper canisters in a repository. However, as one step in the experimental verification it is necessary to study grain boundary corrosion of copper in an environment where it may occur. A literature study aimed to find one or several solutions that are aggressive with respect to grain boundary corrosion of copper. Copper specimens cut from welds of real copper canisters where exposed to aerated ammonium hydroxide solution for a period of 14 days at 80 degrees C and 10 bar pressure. The samples were investigated prior to exposure using the scanning Kelvin probe technique to characterize anodic and cathodic areas on the samples. The degree of corrosion was determined by optical microscopy. No grain boundary corrosion could be observed in the autoclave experiments, however, a higher rate of corrosion was observed for the weld material compared to the base material. The work suggests that grain boundary corrosion of copper weld material is most unlikely to adversely affect SKB's copper canisters under the conditions in the repository

Grain boundary corrosion of copper canister weld material

Energy Technology Data Exchange (ETDEWEB)

Gubner, Rolf; Andersson, Urban; Linder, Mats; Nazarov, Andrej; Taxen, Claes [Corrosion and Metals Research Inst. (KIMAB), Stockholm (Sweden)

2006-01-15

The proposed design for a final repository for spent fuel and other long-lived residues in Sweden is based on the multi-barrier principle. The waste will be encapsulated in sealed cylindrical canisters, which will then be placed in granite bedrock and surrounded by compacted bentonite clay. The canister design is based on a thick cast inner container fitted inside a corrosion-resistant copper canister. During fabrication of the outer copper canisters there will be some unavoidable grain growth in the welded areas. As grains grow, they will tend to concentrate impurities within the copper at the new grain boundaries. The work described in this report was undertaken to determine whether there is any possibility of enhanced corrosion at grain boundaries within the copper canister, based on the recommendations of the report SKB-TR--01-09 (INIS ref. 32025363). Grain boundary corrosion of copper is not expected to be a problem for the copper canisters in a repository. However, as one step in the experimental verification it is necessary to study grain boundary corrosion of copper in an environment where it may occur. A literature study aimed to find one or several solutions that are aggressive with respect to grain boundary corrosion of copper. Copper specimens cut from welds of real copper canisters where exposed to aerated ammonium hydroxide solution for a period of 14 days at 80 degrees C and 10 bar pressure. The samples were investigated prior to exposure using the scanning Kelvin probe technique to characterize anodic and cathodic areas on the samples. The degree of corrosion was determined by optical microscopy. No grain boundary corrosion could be observed in the autoclave experiments, however, a higher rate of corrosion was observed for the weld material compared to the base material. The work suggests that grain boundary corrosion of copper weld material is most unlikely to adversely affect SKB's copper canisters under the conditions in the repository.

The Metal And Sulphate Removal From Mine Drainage Waters By Biological-Chemical Ways

Directory of Open Access Journals (Sweden)

Jenčárová Jana

2015-06-01

Full Text Available Mine drainage waters are often characterized by high concentrations of sulphates and metals as a consequence of the mining industry of sulphide minerals. The aims of this work are to prove some biological-chemical processes utilization for the mine drainage water treatment. The studied principles of contamination elimination from these waters include sulphate reduction and metal bioprecipitation by the application of sulphate-reducing bacteria (SRB. Other studied process was metal sorption by prepared biogenic sorbent. Mine drainage waters from Slovak localities Banská Štiavnica and Smolník were used to the pollution removal examination. In Banská Štiavnica water, sulphates decreased below the legislative limit. The elimination of zinc by sorption experiments achieved 84 % and 65 %, respectively.

Electric field-induced hole transport in copper(i) thiocyanate (CuSCN) thin-films processed from solution at room temperature

KAUST Repository

Pattanasattayavong, Pichaya; Ndjawa, Guy Olivier Ngongang; Zhao, Kui; Chou, Kang Wei; Yaacobi-Gross, Nir; O'Regan, Brian C.; Amassian, Aram; Anthopoulos, Thomas D.

2013-01-01

The optical, structural and charge transport properties of solution-processed films of copper(i) thiocyanate (CuSCN) are investigated in this work. As-processed CuSCN films of ∼20 nm in thickness are found to be nano-crystalline, highly transparent and exhibit intrinsic hole transporting characteristics with a maximum field-effect mobility in the range of 0.01-0.1 cm2 V-1 s-1. © 2013 The Royal Society of Chemistry.

Volcanic lake systems as terrestrial analogue for sulphate-rich terrains on Mars

NARCIS (Netherlands)

Rodríguez, A.

2016-01-01

Remote-sensing observations and rover missions have documented the abundant presence of sulphate-rich mineral associations on the surface of Mars. Together with widespread occurrences of silica and frequent enrichments of chlorine and bromine in soils and rocks, the sulphate associations are

Impact of chlorinated disinfection on copper corrosion in hot water systems

Energy Technology Data Exchange (ETDEWEB)

Montes, J. Castillo [Centre Scientifique et Technique du Bâtiment Nantes, 11 rue Henri Picherit, BP 82341, 44323 Nantes Cedex 03 (France); Laboratoire des Sciences de l’Ingénieur pour l’Environnement, UMR-CNRS 7356, Université de La Rochelle, Avenue Michel Crépeau, 17042 La Rochelle Cedex 1 (France); Hamdani, F. [Laboratoire des Sciences de l’Ingénieur pour l’Environnement, UMR-CNRS 7356, Université de La Rochelle, Avenue Michel Crépeau, 17042 La Rochelle Cedex 1 (France); Creus, J., E-mail: jcreus@univ-lr.fr [Laboratoire des Sciences de l’Ingénieur pour l’Environnement, UMR-CNRS 7356, Université de La Rochelle, Avenue Michel Crépeau, 17042 La Rochelle Cedex 1 (France); Touzain, S. [Laboratoire des Sciences de l’Ingénieur pour l’Environnement, UMR-CNRS 7356, Université de La Rochelle, Avenue Michel Crépeau, 17042 La Rochelle Cedex 1 (France); Correc, O. [Centre Scientifique et Technique du Bâtiment Nantes, 11 rue Henri Picherit, BP 82341, 44323 Nantes Cedex 03 (France)

2014-09-30

Highlights: • Impact of disinfectant treatment on the durability of copper pipes. • Synergy between disinfectant concentration and temperature. • Pitting corrosion of copper associated to the corrosion products formation on copper. - Abstract: In France, hot water quality control inside buildings is occasionally ensured by disinfection treatments using temperature increases or addition of sodium hypochlorite (between 0.5 ppm and 1 ppm residual free chlorine). This disinfectant is a strong oxidiser and it could interact with metallic pipes usually used in hot water systems. This work deals with the study of the impact of these treatments on the durability of copper pipes. The objective of this work was to investigate the influence of sodium hypochlorite concentration and temperature on the copper corrosion mechanism. Copper samples were tested under dynamic and static conditions of ageing with sodium hypochlorite solutions ranging from 0 to 100 ppm with temperature at 50 °C and 70 °C. The efficiency of a corrosion inhibitor was investigated in dynamic conditions. Visual observations and analytical analyses of the internal surface of samples was studied at different ageing duration. Corrosion products were characterised by X-ray diffraction and Raman spectroscopy. Temperature and disinfectant were found to considerably affect the copper corrosion mechanism. Surprisingly, the corrosiveness of the solution was higher at lower temperatures. The temperature influences the nature of corrosion products. The protection efficiency is then strongly depend on the nature of the corrosion products formed at the surface of copper samples exposed to the aggressive solutions containing different concentration of disinfectant.

X-ray CT Scanning Reveals Long-Term Copper Pollution Effects on Functional Soil Structure

DEFF Research Database (Denmark)

Naveed, Muhammad; Møldrup, Per; Homstrup, Martin

Soil structure plays the main role in the ability of the soil to fulfill essential soil functions such as the root growth, rate of water infiltration and retention, transport of gaseous and chemicals/pollutants through the soil. Soil structure is a dynamic soil property and affected by various...... factors such as soil type, land use, and soil contamination. In this study, we quantified the soil structure using X-ray CT scanning and revealed the effect of a long history of Copper (Cu) pollution on it. A fallow field at Hygum Denmark provides this opportunity as it had a long history of Copper...... sulphate contamination in a gradient with Cu content varies from 21 mg kg-1 to 3837 mg kg-1. Total 20 intact soil columns (diameter of 10 cm and height of 8 cm) were sampled at five locations along the Cu-gradient from a depth of 5 to 15 cm below surface level. The soil columns were scanned at a voxel...

Low-cost copper complexes as p-dopants in solution processable hole transport layers

Energy Technology Data Exchange (ETDEWEB)

Kellermann, Renate [Department for Materials Science and Engineering, Chair for Materials for Electronics and Energy Technology, Friedrich-Alexander-University Erlangen-Nuremberg, Erlangen 91058 (Germany); Siemens AG – Corporate Technology, Guenther-Scharowsky-Str. 1, Erlangen 91058 (Germany); Taroata, Dan; Maltenberger, Anna; Hartmann, David; Schmid, Guenter [Siemens AG – Corporate Technology, Guenther-Scharowsky-Str. 1, Erlangen 91058 (Germany); Brabec, Christoph J. [Department for Materials Science and Engineering, Chair for Materials for Electronics and Energy Technology, Friedrich-Alexander-University Erlangen-Nuremberg, Erlangen 91058 (Germany)

2015-09-07

We demonstrate the usage of the Lewis-acidic copper(II)hexafluoroacetylacetonate (Cu(hfac){sub 2}) and copper(II)trifluoroacetylacetonate (Cu(tfac){sub 2}) as low-cost p-dopants for conductivity enhancement of solution processable hole transport layers based on small molecules in organic light emitting diodes (OLEDs). The materials were clearly soluble in mixtures of environmentally friendly anisole and xylene and spin-coated under ambient atmosphere. Enhancements of two and four orders of magnitude, reaching 4.0 × 10{sup −11} S/cm with a dopant concentration of only 2 mol% Cu(hfac){sub 2} and 1.5 × 10{sup −9} S/cm with 5 mol% Cu(tfac){sub 2} in 2,2′,7,7′-tetra(N,N-ditolyl)amino-9,9-spiro-bifluorene (spiro-TTB), respectively, were achieved. Red light emitting diodes were fabricated with reduced driving voltages and enhanced current and power efficiencies (8.6 lm/W with Cu(hfac){sub 2} and 5.6 lm/W with Cu(tfac){sub 2}) compared to the OLED with undoped spiro-TTB (3.9 lm/W). The OLED with Cu(hfac){sub 2} doped spiro-TTB showed an over 8 times improved LT{sub 50} lifetime of 70 h at a starting luminance of 5000 cd/m{sup 2}. The LT{sub 50} lifetime of the reference OLED with PEDOT:PSS was only 8 h. Both non-optimized OLEDs were operated at similar driving voltage and power efficiency.

In situ recovery of copper from sulfide ore bodies following nuclear fracturing

Energy Technology Data Exchange (ETDEWEB)

Rosenbaum, Joe B; McKinney, W A [Salt Lake City Metallurgy Research Center, Bureau of Mines, US Department of the Interior, Salt Lake City, UT (United States)

1970-05-15

Leaching now yields about 12 percent of the Nation's annual new copper production. About 200,000 tons of copper a year is being won by heap and vat leaching of ore, dump leaching of waste, and in-place leaching of caved underground workings. Although in-place leaching was practiced as long ago as the 15th century, it is little used and contributes only a few percent of the total leach copper production. Current technology in this area is exemplified by practice at the Miami, Ariz., mine of the Miami Copper Co. Despite its limited use, the concept of extracting copper by in-place leaching without physically mining and transporting the ore continues to present intriguing cost saving possibilities. Project SLOOP has been proposed as an experiment to test the feasibility of nuclear fracturing and acid leaching the oxidized portion of a deep ore body near Safford, Ariz. However, the bulk of the copper in deep ore deposits occurs as sulfide minerals that are not easily soluble in acid solutions. This paper explores the concept of in-place leaching of nuclear fractured, deeply buried copper sulfide deposits. On the assumption that fracturing of rock and solution injection and collection would be feasible, an assessment is made of solution systems that might be employed for the different copper sulfide minerals in porphyry ore bodies. These include the conventional ferric sulfate-sulfuric acid systems and combinations of sulfide mineral oxidants and different acids. (author)

In situ recovery of copper from sulfide ore bodies following nuclear fracturing