scholarly journals Exceptional Tl-bearing manganese oxides from Zalas, Krakow area, southern Poland

Mineralogia ◽  
2015 ◽  
Vol 46 (1-2) ◽  
pp. 3-17 ◽  
Author(s):  
Bożena Gołębiowska ◽  
Grzegorz Rzepa ◽  
Adam Pieczka

AbstractIn the Permian rhyodacite quarry at Zalas near Krakow, southern Poland, thallium-bearing Mn oxides occur in a small fault zone cutting Middle Jurassic sandy limestone poorly encrusted by an oxidized polymetallic mineralization. The encrustation comprises sulphides (pyrite, chalcopyrite, chalcocite, covellite, galena, marcasite), native bismuth, hematite, goethite, cuprite, mottramite, iodargyrite, unrecognized Cu sulphates and Bi oxychlorides as supergene minerals, barite and rare tiny grains of gold. It is most likely connected with rejuvenation of Early-Paleozoic faults during the Alpine orogeny on the Oligocene–Miocene boundary. Rare Tlbearing Mn oxides occur in an outside zone of the encrustations, filling small fractures and voids in limestone forming the fault breccia. Tl contents, reaching 20.82wt% as Tl2O, exceed by more than two orders of magnitude those reported in similar minerals before, making the oxides unique on a world scale. The Tl-bearing Mn oxides from Zalas reflect intensive weathering of an older Tl-bearing sulphide mineralization in an arid climate, involving saline fluids delivered to the groundwater system as the nappe structure of the Carpathians was developing during the Sava tectonic phase Oligocene/Miocene boundary.

2014 ◽  
Vol 16 (9) ◽  
pp. 2127-2136 ◽  
Author(s):  
Yuanzhi Tang ◽  
Samuel M. Webb ◽  
Emily R. Estes ◽  
Colleen M. Hansel

Manganese (Mn) oxides, which are generally considered biogenic in origin within natural systems, are the only oxidants of Cr(iii) under typical environmental conditions.


2016 ◽  
Vol 42 (1) ◽  
pp. 120
Author(s):  
Marta Polak ◽  
Bożena Gołębiowska ◽  
Grzegorz Rzepa

2019 ◽  
Vol 7 (25) ◽  
pp. 15215-15224 ◽  
Author(s):  
Juliette Billaud ◽  
Denis Sheptyakov ◽  
Sébastien Sallard ◽  
Daniela Leanza ◽  
Michael Talianker ◽  
...  

The addition of Fe in Li-rich nickel cobalt manganese oxides allows for higher specific charge, potential drop mitigation and enhanced rate capability.


2018 ◽  
Vol 8 (24) ◽  
pp. 6493-6502 ◽  
Author(s):  
Homer C. Genuino ◽  
Diego Valencia ◽  
Steven L. Suib

Experimental and computational studies on the properties of Mo-substituted octahedral molecular sieve Mn oxides provide insights into their excellent catalytic activities and stability for CO oxidation.


2011 ◽  
Vol 295-297 ◽  
pp. 1669-1674
Author(s):  
Zhao Jun Deng ◽  
Jing Liu ◽  
Zhi Hong Lu ◽  
Hui Wang ◽  
Cheng Jiang Lin

The morphology of inhibition layer and adhesion of Zn coating about a 600MPa grade high Al dual phase steel were studied by grow discharge spectrometry (GDS), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The results show that the inhibition layer is mainly composed of Fe2Al5-xZnx particles with a size of 0.5~1μm, and the adhesion is directly related to the density of the inhibition layer, the denser the inhibition layer, the better the adhesion. It is found: for the samples with good adhesion that besides the Fe2Al5-xZnx particles, there are also some small spherical Al-Mn oxides particles in sizes from 30 to 100nm uniformly distributed in the inhibition layer; for the samples with bad adhesion, the steel substrate is not fully covered by Fe2Al5-xZnx particles and large amount manganese oxides are detected at the non-covered positions.


2019 ◽  
Vol 6 (5) ◽  
pp. 190122 ◽  
Author(s):  
Toru Hayashi ◽  
Nadège Bonnet-Mercier ◽  
Akira Yamaguchi ◽  
Kazumasa Suetsugu ◽  
Ryuhei Nakamura

The performance of four polymorphs of manganese (Mn) dioxides as the catalyst for the oxygen evolution reaction (OER) in proton exchange membrane (PEM) electrolysers was examined. The comparison of the activity between Mn oxides/carbon (Mn/C), iridium oxide/carbon (Ir/C) and platinum/carbon (Pt/C) under the same condition in PEM electrolysers showed that the γ-MnO 2 /C exhibited a voltage efficiency for water electrolysis comparable to the case with Pt/C, while lower than the case with the benchmark Ir/C OER catalyst. The rapid decrease in the voltage efficiency was observed for a PEM electrolyser with the Mn/C, as indicated by the voltage shift from 1.7 to 1.9 V under the galvanostatic condition. The rapid deactivation was also observed when Pt/C was used, indicating that the instability of PEM electrolysis with Mn/C is probably due to the oxidative decomposition of carbon supports. The OER activity of the four types of Mn oxides was also evaluated at acidic pH in a three-electrode system. It was found that the OER activity trends of the Mn oxides evaluated in an acidic aqueous electrolyte were distinct from those in PEM electrolysers, demonstrating the importance of the evaluation of OER catalysts in a real device condition for future development of noble-metal-free PEM electrolysers.


Minerals ◽  
2019 ◽  
Vol 9 (4) ◽  
pp. 226 ◽  
Author(s):  
Sánchez-España ◽  
Yusta

Manganese oxides are widespread in soils and natural waters, and their capacity to adsorb different trace metals such as Co, Ni, or Zn is well known. In this study, we aimed to compare the extent of trace metal coprecipitation in different Mn oxides formed during Mn(II) oxidation in highly concentrated, metal-rich mine waters. For this purpose, mine water samples collected from the deepest part of several acidic pit lakes in Spain (pH 2.7–4.2), with very high concentration of manganese (358–892 mg/L Mn) and trace metals (e.g., 795–10,394 µg/L Ni, 678–11,081 µg/L Co, 259–624 mg/L Zn), were neutralized to pH 8.0 in the laboratory and later used for Mn(II) oxidation experiments. These waters were subsequently allowed to oxidize at room temperature and pH = 8.5–9.0 over several weeks until Mn(II) was totally oxidized and a dense layer of manganese precipitates had been formed. These solids were characterized by different techniques for investigating the mineral phases formed and the amount of coprecipitated trace metals. All Mn oxides were fine-grained and poorly crystalline. Evidence from X-Ray Diffraction (XRD) and Scanning Electron Microscopy coupled to Energy Dispersive X-Ray Spectroscopy (SEM–EDX) suggests the formation of different manganese oxides with varying oxidation state ranging from Mn(III) (e.g., manganite) and Mn(III/IV) (e.g., birnessite, todorokite) to Mn(IV) (e.g., asbolane). Whole-precipitate analyses by Inductively Coupled Plasma-Mass Spectrometry (ICP-MS), Inductively Coupled Plasma-Atomic Emission Spectrometry (ICP-AES), and/or Atomic Absorption Spectrometry (AAS), provided important concentrations of trace metals in birnessite (e.g., up to 1424 ppm Co, 814 ppm Ni, and 2713 ppm Zn), while Co and Ni concentrations at weight percent units were detected in asbolane by SEM-EDX. This trace metal retention capacity is lower than that observed in natural Mn oxides (e.g., birnessite) formed in the water column in a circum-neutral pit lake (pH 7.0–8.0), or in desautelsite obtained in previous neutralization experiments (pH 9.0–10.0). However, given the very high amount of Mn sorbent material formed in the solutions (2.8–4.6 g/L Mn oxide), the formation of these Mn(III/IV) oxides invariably led to the virtually total removal of Co, Ni, and Zn from the aqueous phase. We evaluate these data in the context of mine water pollution treatment and recovery of critical metals.


2014 ◽  
Vol 43 (34) ◽  
pp. 13122-13135 ◽  
Author(s):  
Mohammad Mahdi Najafpour ◽  
Małgorzata Hołyńska ◽  
Amir Nasser Shamkhali ◽  
Sayed Habib Kazemi ◽  
Warwick Hillier ◽  
...  

Mn oxides may be true catalysts in the water-oxidation reactions of Mn complexes and oxidants.


2017 ◽  
Vol 7 (16) ◽  
pp. 3499-3510 ◽  
Author(s):  
Mohammad Mahdi Najafpour ◽  
Navid Jameei Moghaddam ◽  
Seyedeh Maedeh Hosseini ◽  
Sepideh Madadkhani ◽  
Małgorzata Hołyńska ◽  
...  
Keyword(s):  

The electrochemistry of nanolayered Mn oxides in the presence of LiClO4 at pH = 6.3 under different conditions was studied.


2009 ◽  
Vol 71-73 ◽  
pp. 633-636 ◽  
Author(s):  
Keiko Sasaki ◽  
T. Kaseyama ◽  
Tsuyoshi Hirajima

Unique properties of biogenic Mn oxides were applied to a fundamental study of separation and recovery of rare earth elements. Selective sorption of Ce3+ over La3+ ions was achieved at neutral pH values using biogenic Mn oxides produced by Paraconiothyrium sp. WL-2 strain. The selective coefficient for Ce3+ (αCe) was much greater with biogenic and synthetic Mn oxides than those for La3+ (αLa). Ce3+ ions were oxidized to CeO2 by Mn(III, IV) in Mn oxides under anaerobic conditions resulting in the release of Mn2+ ions, while La3+ ions were sorbed without a redox reaction. With an increase in coexisting La3+ ions, sorption of Ce3+ on both Mn oxides was significantly suppressed, especially with synthetic Mn oxides. The edges of the structure are competitive sites because of fewer numbers of vacant sites in synthetic Mn oxide layers. The preferential sorption on the edge sites of Mn oxides is in the order of La3+ > Ce3+. These phenomena can be expanded to separation and recovery of other rare earth elements from natural and anthropogenic sources.


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