Mobility of antimony in samples from diverse environmental compartments of Sb mines in Spain: leaching experiments in oxidizing and reducing conditions

Author(s):  
Fabienne Battaglia-Brunet ◽  
Hugues Thouin ◽  
José Maria Esbri Victor ◽  
Eva Maria Garcia Noguero ◽  
Saturnino Lorenzo ◽  
...  

<p>Antimony (Sb) is a valuable element, exploited for diverse applications including flame retardants, munitions, batteries, glasses, and industry for diodes. However Sb is also a toxic metalloid, often associated with other harmful elements (arsenic, lead, mercury…) in mining sites. The biogeochemical behavior of Sb remains poorly documented, and data must be acquired in order to elaborate solid environmental studies related with Sb mining. Here, the mobility of Sb from solid phases present in former mining sites was assessed through leaching experiments performed in oxidizing or reducing conditions. Five Sb mines located in South-Central Spain were considered: La Nazarena, Accesos, Balanzona, Pilar, and Susana mines. Rock samples were analysed by X-ray diffraction, confirming that the main Sb carrier was stibnite (Sb<sub>2</sub>S<sub>3</sub>), present in all mines. Surface soils and mine wastes were sampled, together with sediments when ponds or galleries were present. The total Sb concentrations of 18 samples varied from 28 to 221 000 mg kg<sup>-1</sup>. However, stibnite was only detected in a soil sample from Balanzona mine and tetrahedrite ((Cu,Fe)<sub>12</sub>Sb<sub>4</sub>S<sub>13</sub>)<sub></sub>in a sediment from the Balanzona mine. The most common Sb secondary minerals were bindheimite (Pb<sub>2</sub>Sb<sub>2</sub>O<sub>6</sub>O), senarmontite (Sb<sub>2</sub>O<sub>3</sub>), valentinite (Sb<sub>2</sub>O<sub>3</sub>) and stenhuggarite (CaFeSb(AsO<sub>3</sub>)<sub>2</sub>O). These materials were incubated in slurries at 10 % solids, at 25°C under agitation, either in presence of air or under N<sub>2</sub>/H<sub>2</sub> atmosphere. Sb was generally more mobile in oxidizing conditions; however, for 2 samples, mobility was higher in reducing conditions. The highest Sb concentrations in water were in the range 20 to 30 mg L<sup>-1</sup>. The final percentage of solubilized Sb exceeded 1 % (between 1 and 12 %) for 10 samples. For one sediment sampled in Balanzola mine, final Sb concentrations were close to 20 mg L<sup>-1</sup> in oxidizing conditions and 10 mg L<sup>-1</sup> in reducing conditions. Acidification was observed with several samples; however, Sb release was not systematically related with the evolution of pH. The mobility of Sb during leaching might be driven by diverse mechanisms: release of sorbed Sb, abiotic or biotic dissolution of Sb-bearing minerals, including oxidation of Sb sulfides in aerobic conditions, or reductive dissolution of Sb-bearing iron or manganese oxides, and finally release of soluble thio-Sb complexes in anaerobic conditions. Supporting the occurrence of these last mechanisms, final analyses indicated solubilization of Fe and Mn and traces of dissolved sulfide in reducing conditions. Our results, that showed a higher mobility of Sb in oxidizing conditions, are globally consistent with previous works indicating a higher occurrence of the oxidized form of Sb, i.e. Sb<sup>V</sup>, in water streams impacted by mining sites. However, we also observed that non negligible release of Sb can be linked to mechanisms occurring in reducing conditions. Perspectives of this work include the elucidation of the biological processes, directly or indirectly involved in Sb release or immobilisation, in order to better predict the evolution of environmental quality on mining sites and propose remediation strategies.</p><p>This work was funded by the ANR (ANR-19-MIN2-0002-01), the AEI (MICIU/AEI/REF.: PCI2019-103779) and author’s institutions in the framework of the ERA-MIN2 AUREOLE project.</p>

2011 ◽  
Vol 189-193 ◽  
pp. 1208-1211 ◽  
Author(s):  
Yan Shen ◽  
Shao Guo Wen ◽  
Ji Hu Wang ◽  
Hong Bo Liu ◽  
Hai Liang Qi ◽  
...  

In this paper, flame retardant Polyamide 6 (PA6) composites were prepared by nano-magnesium hydroxide (NMH) or its composites with melamine cyanurate(MCA) and ammonium polyphosphate(APP). Scanning electron microscopy (SEM) and X-ray diffraction (XRD) were used to analyze the structure of nano-magnesium hydroxide. The properties including tensile properties, molten index (MFI), rockwell hardness and density of flame retardant PA6 were analyzed. Orthogonal experiments were used to study flame retardancy of PA6 with NMH, MCA and APP. The results showed NMH had hexagonal orthorhombic crystal structure with size of 300×200×100nm. Density of polyamide 6 showed an upward trend when the content of NMH was increasing, the mechanical properties and hardness changed little while processing performance serious declined. The flame retardance of nitrogen-phosphorus -inorganic flame retardants was not desirable.


2017 ◽  
Vol 52 (10) ◽  
pp. 1295-1303 ◽  
Author(s):  
Yijiao Xue ◽  
Mingxia Shen ◽  
Fengling Lu ◽  
Yongqin Han ◽  
Shaohua Zeng ◽  
...  

To improve the flame resistance of polystyrene, three kinds of organophilic heterionic montmorillonites (Na-montmorillonite, Ca-montmorillonite, and Fe-montmorillonite) reinforced polystyrene nanocomposites were prepared by melt dispersion method. The structure and composition of the organo montmorillonites were characterized by using X-ray diffraction and Fourier-transform infrared analysis. The adhesion between organo montmorillonites and polystyrene was investigated by scanning electron microscopy. The flame resistance and thermal stability of the polystyrene/organo montmorillonites were evaluated by cone calorimeter test and thermogravimetric analysis. The interlayer space of organo montmorillonites increased with the increase of the oxidation state of the cations. With the addition of organo montmorillonites, the peak values of all the flame resistance indexes of the polystyrene/organo montmorillonites nanocomposites decreased, among which the PHRR values have decreased the most, compared with those of polystyrene. Their corresponding test times have all been delayed following almost precisely the same trend. Therefore, their flame retardant ability come from their lamellated structures, their charring forming abilities, and the reducing power of Fe3+ in polystyrene/Fe-montmorillonite. Organo montmorillonites mainly act as a kind of intumescent flame retardants. The flame resistance of polystyrene/Na-montmorillonite nanocomposite was the best, and the polystyrene/Ca-montmorillonite came second, which is slightly better than that of polystyrene/Fe-montmorillonite.


2017 ◽  
Vol 31 (02) ◽  
pp. 1750006 ◽  
Author(s):  
Mohammad Hossein Ghorbani ◽  
Abdol Mahmood Davarpanah

Manganese oxides are of more interest to researchers because of their ability as catalysts and lithium batteries. In this research, MnO2nanowires with diameter about 45 nm were synthesized by sol–gel method at room temperature (RT). Effect of increasing the annealing temperature from 400[Formula: see text]C to 600[Formula: see text]C on crystalline structure of nanostructure were studied and average crystallite size was estimated about 22 nm. X-ray Diffraction (XRD) method, Energy-Dispersive X-ray Diffraction (EDXD), Scanning Electron Microscopy (SEM) and Vibrating Sample Magnetometer (VSM) were used to characterize the nanowires of MnO2.


2021 ◽  
Vol 13 (4) ◽  
pp. 569-573
Author(s):  
Xian-Feng Li ◽  
Gui-Qiang Diao ◽  
Fang Xie ◽  
Wen-Hua Liao ◽  
Luigi Agostini ◽  
...  

Manganese oxides have been widely studied as anode materials for lithium-ion batteries because they have many advantages such as high theoretical capacity, abundant resources, low price and low environmental tox-icity. In this paper, various manganese oxide materials, i.e., MnO2, Mn3O4, MnO, (FeO)0.331(MnO)0.669 were prepared by facile methods. The above compounds were then characterized through X-ray diffraction spec-troscopy (XRD). The oxidation states of Mn in these compounds were found to be: +4, +3/+2, +2 and +2 each of them corresponding to a different crystal system, respectively: hexagonal, tetragonal cubic, cubic. The electrochemical properties of these four different manganese oxides, used as anode materials, were investigated to find the possible relationship between their valence states, crystal systems and their electrochemical properties. The results show that their electrochemical properties are influenced by their crystal system and cell parameters, while incorporating FeO into MnO has an activation effect on the reversible lithium ion in the batteries.


1990 ◽  
Vol 45 (6) ◽  
pp. 876-886 ◽  
Author(s):  
Wolfgang A. Herrmann ◽  
Josef K. Felixberger ◽  
Josef G. Kuchler ◽  
Eberhardt Herdtweck

The class of π-alkyne complexes of metals in medium and high oxidation states has been extended by the type CH3ReO2(RC≡CR′) (3a—i). Exchange of alkyne for oxo ligands under reducing conditions has been employed as a new general synthesis. Compounds 3 are thus obtained by reaction of methyltrioxorhenium(VII) (1) with the alkynes 2a—i in the presence of a ca. 1.1-fold molar amount of polymer-bound triphenylphosphane as reducing agent (desoxygenation). The structural characterization was carried out for the example of the tolan complex 3 e by virtue of a single-crystal X-ray diffraction study at —80 °C, according to which the description of compounds 3 as “rhenacyclopropenes” seems justified. Evidence from NMR investigations of 3 a and 3 c shows that no fast rotation of the respective alkyne ligand around the axis to the metal atom occurs on the NMR time scale up to at least 105 °C. A minimal rotation barrier of approximately 20 kcal/mol is thus to be estimated. Reaction of type 3 compounds (R = R′ = CH3, b; R = R′ = C2H5, c) with polymer-bound triphenylphosphane under more drastic conditions (boiling toluene) for two days effects further reduction, with the dinuclear, diamagnetic rhenium(IV) complexes 4b and 4c, resp., being formed. Sterically demanding alkynes (e.g., R = R′ = Si(CH3)3, C6H5) seem to prevent this type of reaction. According to an X-ray diffraction study, 4b has an equilateral Re2O-triangular core geometry, with the ligands O, CH3, and butyne(2) arranged in such a way that C2-symmetry results. The alkyne complexes reported here are the first ones of tetra- and pentavalent rhenium.


1998 ◽  
Vol 13 (11) ◽  
pp. 3181-3190 ◽  
Author(s):  
B. D. Begg ◽  
E. R. Vance ◽  
B. A. Hunter ◽  
J. V. Hanna

The structural behavior of zirconolite (CaZrTi2O7) under reducing conditions at high temperature has been studied, mainly by scanning electron microscopy (SEM) and x-ray diffraction (XRD), but also with x-ray absorption spectroscopy, thermogravimetry, and electron paramagnetic resonance. The partial reduction of Ti4+ to Ti3+, associated with a reducing atmosphere heat treatment, led to the initial formation of perovskite (CaTiO3) as a second phase. As the concentration of Ti3+ in the zirconolite increased, so did the amount of perovskite until the zirconolite was totally transformed into a fluorite structured phase. Analysis of the reduced zirconolites showed them to be consistently deficient in Ca and enriched in Zr, in proportion to the concentration of Ti3+. To determine how electroneutrality was preserved in these reduced zirconolites, a series of zirconolites were prepared in air using In3+ and Ga3+ as models for Ti3+. These samples were then investigated by neutron and x-ray diffraction, SEM, solid state nuclear magnetic resonance (NMR), and nuclear quadrupole resonance (NQR). 71Ga MAS NMR studies of the Ga substituted zirconolite exhibited a narrow resonance at ˜13 ppm which was attributed to six-coordinate Ga incorporated in a trace perovskite phase. Broadline 71Ga NMR and 69/71Ga NQR were required to characterize the Ga incorporated in the zirconolite. The resultant quadrupolar parameters of CQ = 30.0 ± 0.05 MHz and η = 1.0 ± 0.03 indicate that the Ga site is in a highly distorted environment which would suggest that it is located on the five-coordinate Ti site within the zirconolite lattice. These results were complemented by Rietveld refinement of the neutron diffraction data from the In-doped zirconolite sample, which was optimal when all the In was located on the five-coordinate Ti site with the excess Zr located on the Ca site. It would therefore appear that charge compensation for the presence of Ti3+ in zirconolite is effected via the substitution of an appropriate amount of Zr on the Ca site. The Ti3+-stabilized fluorite structure was readily oxidized back to a single phase zirconolite upon heating in air.


2003 ◽  
Vol 807 ◽  
Author(s):  
A. G. Ptashkin ◽  
S. V. Stefanovsky ◽  
S. V. Yudintsev ◽  
S. A. Perevalov

ABSTRACTPu-bearing zirconolite and pyrochlore based ceramics were prepared by melting under oxidizing and reducing conditions at 1550 °C. 239Pu content in the samples ranged between ∼10 and ∼50 wt.%. Phase composition of the ceramics and Pu partitioning were studied using X-ray diffraction (XRD) and scanning electron microscopy with energy dispersive system (SEM/EDS). Major phases in the samples were found to be the target zirconolite and pyrochlore as well as a cubic fluorite structure oxide. Normally the Pu content in the Pu host phases was 10–12 wt.%. This corresponds to the Pu content recommended for matrices for immobilization of excess weapons plutonium. At higher Pu content (up to 50 wt.%) additional phases, such as a PuO2-based cubic fluorite-structured solid solution, perovskite, and rutile were found.


2004 ◽  
Vol 824 ◽  
Author(s):  
A.S. Aloy ◽  
A.V. Trofimenko ◽  
O.A. Iskhakova ◽  
L.J. Jardine

AbstractThe results of the studies of uranium valent states in the borosilicate glasses incorporating the components of uranium-containing sludge of Mining and Chemical Combine (MCC, Zheleznogorsks.) is presented in this work. The glasses were made under oxidative and reducing conditions.The optical spectrophotometry, nuclear gamma-resonance (NGR) and X-ray diffraction (XRD) showed that glasses produced under oxidative conditions are characterized by the presence of only U(6+), while U(4+) in the reducing conditions is present along with U(6+). The ratio U(6+)/to U(4+) varies in depending on the synthesis conditions.The glass samples synthesized under oxidative conditions were researched at initial solid state. The others synthesized under reducing conditions was dissolved preliminary without distort of uranium valency.The effect of U(4+)/U(6+) ratio on the uranium leach rates from the glasses has been studied at 90° using MCC-1 test.


2009 ◽  
Vol 1193 ◽  
Author(s):  
Yulia I. Korneyko ◽  
Vladimir M. Garbuzov ◽  
Olga V. Schmidta ◽  
Boris E. Burakov

AbstractImmobilization of long-lived 99Tc requires development of chemically resistant inorganic matrices. Samples of ceramics based on crystalline Fe-Mn- and Zr-Mn-oxide compounds were synthesized at 1150°C in air, reducing or inert atmosphere from precursors doped with 5-12 wt.% Tc. All the samples obtained were studied using optical and scanning electron microscopy (SEM); powder X-ray diffraction (XRD) and microprobe analysis (EMPA). Content of Tc varied from 0.5-0.8 to 3-6 wt.% in oxide host phases and from 54 to 93 wt.% in metallic inclusions. It was demonstrated that synthesis of oxide host-phases under oxidizing or reducing conditions was not optimal due to partial Tc volatilization or metallic phase formation, respectively. The use of inert atmosphere for ceramic synthesis supports Tc incorporation into crystalline structure of stable host-phases. Development of optimal methods of precursor preparation and synthesis conditions of Tc-doped ceramic are being discussed.


1993 ◽  
Vol 333 ◽  
Author(s):  
S. Stroes-Gascoyne ◽  
J.C. Tait ◽  
R.J. Porth ◽  
J.L. McConnell ◽  
A.M. Duclos

ABSTRACTThe separate effects of alpha- and gamma-radiolysis on UO2dissolution can be studied with unirradiated UO2, whereas studies vith used nuclear fuel necessarily always include both alpha- and gamma-radiolysis effects. This paper attempts to separate these effects by comparing the leaching behaviour in saline solution of a number of UO2samples (each vith a particular radiation characteristic or chemical property inherent to used fuel) vith the leaching behaviour of used fuel. Data from leaching experiments vith lov- and high-burnup CANDU (CANada Deuterium Uranium) fuels are also compared. The results indicate that the presence of an alpha field at 100°C under reducing conditions does not increase UO2dissolution but suggest that the combined effects of the beta and gamma fields in used CANDU fuel may enhance UO2dissolution.


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