scholarly journals Role of Ag+ in the Bioleaching of Arsenopyrite by Acidithiobacillus ferrooxidans

Metals ◽  
2020 ◽  
Vol 10 (3) ◽  
pp. 403
Author(s):  
Yan Zhang ◽  
Qian Li ◽  
Xiaoliang Liu
Keyword(s):  
Photoelectron Spectroscopy ◽  
Acidithiobacillus Ferrooxidans ◽  
Large Scale ◽  
Low Cost ◽  
Xrd Analysis ◽  
Green Technology ◽  
Environmental Friendliness ◽  
X Ray ◽  
Pre Treatment

Arsenopyrite (FeAsS) is often associated with gold, but pre-treatment is necessary prior to gold leaching, mainly due to the gold encapsulation in the matrix of FeAsS. Bio-oxidation is attractive and promising, largely due to its simplicity, low cost and environmental friendliness. A critical problem that still impedes the large-scale applications of this green technology is its slow leaching kinetics. Some metal ions such as Ag+ have previously been found to expedite the bioleaching process. In this paper, the role of Ag+ in the arsenopyrite bioleaching by Acidithiobacillus ferrooxidans was investigated in detail by bioleaching experiments and a series of analyses including thermodynamics, X-ray diffraction (XRD), scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS). Experimental results suggested that addition of 5 mg/L Ag+ to the leaching system could significantly improve the final As leaching efficiency from 30.4% to 47.8% and shorten the bioleaching period from 19 days to 15 days. Thermodynamic analysis indicates that Ag+ destabilises As2S2, As2S3 and S0 via forming Ag2S, which is confirmed by the XRD analysis on the phase transformation during bioleaching. SEM and XPS analyses further showed that Ag+ removed the passivating film consisting mainly of As2S2, As2S3 and S0 because Ag2S formed on the arsenopyrite surface from the start bioleaching of 36 h. In the presence of Fe3+, Ag2S could easily be dissolved to Ag+ again, likely leading to the establishment of the Ag+/Ag2S cycle. The bacteria utilised the two synergistic cycles of Fe3+/Fe2+ and Ag+/Ag2S to catalyse the bioleaching of arsenopyrite.

scholarly journals Formation Process of the Passivating Products from Arsenopyrite Bioleaching by Acidithiobacillus ferrooxidans in 9K Culture Medium

Metals ◽  
2019 ◽  
Vol 9 (12) ◽  
pp. 1320 ◽  
Author(s):  
Xiaoliang Liu ◽  
Qian Li ◽  
Yan Zhang ◽  
Yongbin Yang ◽  
Bin Xu ◽  
...  
Keyword(s):  
Formation Process ◽  
Acidithiobacillus Ferrooxidans ◽  
Large Scale ◽  
Culture Medium ◽  
Low Cost ◽  
Sulphide Mineral ◽  
Environmental Friendliness ◽  
Passivating Film ◽  
Pre Treatment ◽  
Significant Attention

Arsenopyrite is a common sulphide mineral occurring in deposits of gold ore that makes the extraction of gold difficult and, thus, pre-treatment is necessary prior to gold leaching. Bioleaching pre-treatment of arsenopyrite has drawn significant attention owing to its environmental friendliness, low cost and simple operation. A critical impedance of bioleaching to its large-scale industrial application is the slow leaching kinetics. Various passivating products on the surface of arsenopyrite have been found to limit the bioleaching process. This paper reports results from an in-depth investigation into the formation process of passivating products from arsenopyrite bioleaching by Acidithiobacillus ferrooxidans in 9K culture medium including bioleaching experiments and physicochemical analyses of the materials as well as thermodynamic analyses of the leaching system. The results of phase transformation and morphological change of the solid products suggest that the passivation occurring in the bioleaching of arsenopyrite is largely attributed to an initially formed passivating film consisting mainly of realgar (As2S2), orpiment (As2S3) and elemental sulphur (S0) on the arsenopyrite surface. Based on the results, the paper also proposes possible passivation mechanisms to allow for a better understanding on the passivation behaviour of the bioleaching of arsenopyrite.

scholarly journals Surface Treatment of Industrial-Grade Magnetite Particles for Enhanced Thermal Stability and Mitigating Paint Contaminants

Nanomaterials ◽  
2021 ◽  
Vol 11 (9) ◽  
pp. 2299
Author(s):  
Mohua Sinhababu ◽  
Anurag Roy ◽  
Narendra Kumar ◽  
Monojit Dutta ◽  
Senthilarasu Sundaram ◽  
...  
Keyword(s):  
Thermal Stability ◽  
Surface Treatment ◽  
Photoelectron Spectroscopy ◽  
Large Scale ◽  
Low Cost ◽  
High Surface ◽  
Color Difference ◽  
X Ray ◽  
Industrial Grade ◽  
Paint Industry

Pigments can retain their color for many centuries and can withstand the effects of light and weather. The paint industry suffers from issues like aggressive moisture, corrosion, and further environmental contamination of the pigment materials. Low-cost, long-lasting, and large-scale pigments are highly desirable to protect against the challenges of contamination that exist in the paint industry. This exploratory study reinforces the color and thermal stability of industrial-grade (IG) magnetite (Fe3O4). IG Fe3O4 pigments were further considered for surface treatment with sodium hexametaphosphate (SHMP). This metaphosphate hexamer sequestrant provides good dispersion ability and a high surface energy giving thermal and dust protection to the pigment. Various physicochemical characterizations were employed to understand the effectiveness of this treatment across various temperatures (180–300 °C). The X-ray diffraction, Raman, and X-ray photoelectron spectroscopy techniques signify that the SHMP-treated Fe3O4 acquired magnetite phase stability up to 300 °C. In addition, the delta-E color difference method was also adopted to measure the effective pigment properties, where the delta-E value significantly decreased from 8.77 to 0.84 once treated with SHMP at 300 °C. The distinct color retention at 300 °C and the improved dispersion properties of surface-treated Fe3O4 positions this pigment as a robust candidate for high-temperature paint and coating applications. This study further encompasses an effort to design low-cost, large-scale, and thermally stable pigments that can protect against UV-rays, dust, corrosion, and other color contaminants that are endured by building paints.

Characterization of carbides in iron Fischer-Tropsch catalysts

1995 ◽  
Vol 53 ◽  
pp. 434-435
Author(s):  
Mehul D. Shroff ◽  
Dinesh S. Kalakkad ◽  
Nancy B. Jackson ◽  
Mark S. Harrington ◽  
Allen G. Sault ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Carbide Phase ◽  
Low Cost ◽  
High Water ◽  
X Ray Diffraction ◽  
Fischer Tropsch ◽  
X Ray ◽  
Water Gas

The Fischer - Tropsch synthesis (FTS) for the production of synthetic hydrocarbons from the indirect liquefaction of coal has tremendous potential as an alternative to petroleum - based fuels. The use of iron catalysts is desirable due to their low cost, easy availability, good FTS activity and high water - gas shift activity thus enabling use with low H2 / CO ratios. However, problems relating to attrition and deactivation need to be addressed. In addition, there has been a controversy in the literature regarding the role of the carbide phase and the identity of the active catalytic phase. The main reason for the existence of this debate has been the use of different characterization techniques. Our results with a commercial, precipitated and spray-dried, Fe2O3 - CuO - K2O Fischer-Tropsch catalyst point to the fact that conventional techniques like X - ray Diffraction (XRD), X - ray Photoelectron Spectroscopy (XPS) and Auger Electron Spectroscopy (AES) which have been traditionally used to characterize these catalysts (1,2) are not very successful in detecting the existence of the carbide phase, which generally forms as 20 - 30 nm crystallites on the surface of the micron - sized magnetite crystals.

scholarly journals Preparation of magnetic carbon/Fe3O4 supported zero-valent iron composites and their application in Pb(II) removal from aqueous solutions

2017 ◽  
Vol 76 (10) ◽  
pp. 2680-2689 ◽  
Author(s):  
Kaixuan Ma ◽  
Qiu Wang ◽  
Qianyun Rong ◽  
Dapeng Zhang ◽  
Shihai Cui ◽  
...  
Keyword(s):  
Removal Efficiency ◽  
Photoelectron Spectroscopy ◽  
Low Cost ◽  
Zero Valent Iron ◽  
Solution Ph ◽  
Environmental Friendliness ◽  
X Ray ◽  
Transmission Electron ◽  
Reduction Methods ◽  
Magnetic Carbon

Abstract Nanoscale zero-valent iron (NZVI) was first assembled on magnetic carbon/Fe3O4 (CM) with a combination of hydrothermal and liquid phase reduction methods. The novel NZVI@CM magnetic nanocomposites have the merits of large surface area, unique magnetic property, low cost and environmental friendliness. They can be used for Pb(II) removal in aqueous solution. The materials were characterized by using transmission electron microscopy (TEM), X-ray diffraction (XRD), Fourier transform-infrared spectroscopy (FT-IR), thermogravimetric analysis (TGA), vibrating sample magnetometry (VSM), X-ray photoelectron spectroscopy (XPS) and Brunauer–Emmett–Teller (BET) adsorption. The various parameters, such as reaction time, dosage of catalyst, solution pH and acid ions concentrations were studied. The removal efficiency of Pb(II) can be obviously increased by the combination of appropriate CM and NZVI. The removal efficiency of Pb(II) is 99.7% by using 60 mg of NZVI@CM at pH 7. The kinetics study indicates that the Pb(II) removal accords to pseudo-second-order kinetics model.

scholarly journals Performance Improvement of ZnSnO Thin-Film Transistors with Low-Temperature Self-Combustion Reaction

Electronics ◽  
2021 ◽  
Vol 10 (9) ◽  
pp. 1099
Author(s):  
Ye-Ji Han ◽  
Se Hyeong Lee ◽  
So-Young Bak ◽  
Tae-Hee Han ◽  
Sangwoo Kim ◽  
...  
Keyword(s):  
Thin Film ◽  
Photoelectron Spectroscopy ◽  
Large Scale ◽  
Low Cost ◽  
Thermal Analyses ◽  
Thin Film Transistor ◽  
Sol Gel ◽  
Annealing Temperatures ◽  
Zinc Tin Oxide ◽  
Thermal Limitation

Conventional sol-gel solutions have received significant attention in thin-film transistor (TFT) manufacturing because of their advantages such as simple processing, large-scale applicability, and low cost. However, conventional sol-gel processed zinc tin oxide (ZTO) TFTs have a thermal limitation in that they require high annealing temperatures of more than 500 °C, which are incompatible with most flexible plastic substrates. In this study, to overcome the thermal limitation of conventional sol-gel processed ZTO TFTs, we demonstrated a ZTO TFT that was fabricated at low annealing temperatures of 350 °C using self-combustion. The optimized device exhibited satisfactory performance, with μsat of 4.72 cm2/V∙s, Vth of −1.28 V, SS of 0.86 V/decade, and ION/OFF of 1.70 × 106 at a low annealing temperature of 350 °C for one hour. To compare a conventional sol-gel processed ZTO TFT with the optimized device, thermogravimetric and differential thermal analyses (TG-DTA) and X-ray photoelectron spectroscopy (XPS) were implemented.

scholarly journals Synthesis of Exosome-Based Fluorescent Gold Nanoclusters for Cellular Imaging Applications

2021 ◽  
Vol 22 (9) ◽  
pp. 4433
Author(s):  
Eun Sung Lee ◽  
Byung Seok Cha ◽  
Seokjoon Kim ◽  
Ki Soo Park
Keyword(s):  
Photoelectron Spectroscopy ◽  
Low Cost ◽  
Stokes Shift ◽  
Gold Nanoclusters ◽  
Human Colon ◽  
Cellular Imaging ◽  
Metal Nanoclusters ◽  
Human Colon Cancer ◽  
X Ray ◽  
High Concentrations

In recent years, fluorescent metal nanoclusters have been used to develop bioimaging and sensing technology. Notably, protein-templated fluorescent gold nanoclusters (AuNCs) are attracting interest due to their excellent fluorescence properties and biocompatibility. Herein, we used an exosome template to synthesize AuNCs in an eco-friendly manner that required neither harsh conditions nor toxic chemicals. Specifically, we used a neutral (pH 7) and alkaline (pH 11.5) pH to synthesize two different exosome-based AuNCs (exo-AuNCs) with independent blue and red emission. Using field-emission scanning electron microscopy, energy dispersive X-ray microanalysis, nanoparticle tracking analysis, and X-ray photoelectron spectroscopy, we demonstrated that AuNCs were successfully formed in the exosomes. Red-emitting exo-AuNCs were found to have a larger Stokes shift and a stronger fluorescence intensity than the blue-emitting exo-AuNCs. Both exo-AuNCs were compatible with MCF-7 (human breast cancer), HeLa (human cervical cancer), and HT29 (human colon cancer) cells, although blue-emitting exo-AuNCs were cytotoxic at high concentrations (≥5 mg/mL). Red-emitting exo-AuNCs successfully stained the nucleus and were compatible with membrane-staining dyes. This is the first study to use exosomes to synthesize fluorescent nanomaterials for cellular imaging applications. As exosomes are naturally produced via secretion from almost all types of cell, the proposed method could serve as a strategy for low-cost production of versatile nanomaterials.

scholarly journals Yttrium doped phosphate-based glasses: structural and degradation analyses

2020 ◽  
Vol 6 (1) ◽  
pp. 34-49
Author(s):  
Abul Arafat ◽  
Sabrin A. Samad ◽  
Jeremy J. Titman ◽  
Andrew L. Lewis ◽  
Emma R. Barney ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Structural Changes ◽  
Xrd Analysis ◽  
Calcium Pyrophosphate ◽  
Ion Release ◽  
Subsequent Increase ◽  
Structural Characterisation ◽  
Release Studies ◽  
Degradation Properties

AbstractThis study investigates the role of yttrium in phosphate-based glasses in the system 45(P2O5)–25(CaO)– (30-x)(Na2O)–x(Y2O3) (0≤x≤5) prepared via melt quenching and focuses on their structural characterisation and degradation properties. The structural analyses were performed using a combination of solid-state nuclear magnetic resonance (NMR), Fourier transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS). 31P NMR analysis showed that depolymerisation of the phosphate network occurred which increased with Y2O3 content as metaphosphate units (Q2) decreased with subsequent increase in pyrophosphate species (Q1). The NMR results correlated well with structural changes observed via FTIR and XPS analyses. XRD analysis of crystallised glass samples revealed the presence of calcium pyrophosphate (Ca2P2O7) and sodium metaphosphate (NaPO3) phases for all the glass formulations explored. Yttrium-containing phases were found for the formulations containing 3 and 5 mol% Y2O3. Degradation analyses performed in Phosphate buffer saline (PBS) and Milli-Q water revealed significantly reduced rates with addition of Y2O3 content. This decrease was attributed to the formation of Y-O-P bonds where the octahedral structure of yttrium (YO6) cross-linked phosphate chains, subsequently leading to an increase in chemical durability of the glasses. The ion release studies also showed good correlation with the degradation profiles.

scholarly journals An Insight into Chemistry and Structure of Colloidal 2D-WS2 Nanoflakes: Combined XPS and XRD Study

Nanomaterials ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 1969
Author(s):  
Riccardo Scarfiello ◽  
Elisabetta Mazzotta ◽  
Davide Altamura ◽  
Concetta Nobile ◽  
Rosanna Mastria ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Xrd Analysis ◽  
Crystal Habit ◽  
Phase Identification ◽  
X Ray Diffraction ◽  
X Ray ◽  
Morphological Evaluation ◽  
Rational Understanding ◽  
Structural Inspection

The surface and structural characterization techniques of three atom-thick bi-dimensional 2D-WS2 colloidal nanocrystals cross the limit of bulk investigation, offering the possibility of simultaneous phase identification, structural-to-morphological evaluation, and surface chemical description. In the present study, we report a rational understanding based on X-ray photoelectron spectroscopy (XPS) and structural inspection of two kinds of dimensionally controllable 2D-WS2 colloidal nanoflakes (NFLs) generated with a surfactant assisted non-hydrolytic route. The qualitative and quantitative determination of 1T’ and 2H phases based on W 4f XPS signal components, together with the presence of two kinds of sulfur ions, S22− and S2−, based on S 2p signal and related to the formation of WS2 and WOxSy in a mixed oxygen-sulfur environment, are carefully reported and discussed for both nanocrystals breeds. The XPS results are used as an input for detailed X-ray Diffraction (XRD) analysis allowing for a clear discrimination of NFLs crystal habit, and an estimation of the exact number of atomic monolayers composing the 2D-WS2 nanocrystalline samples.

Influence of High Current Pulsed Electron Beam Irradiation on Ni-P Electroless Plating

2011 ◽  
Vol 299-300 ◽  
pp. 77-81
Author(s):  
Yang Xu ◽  
Sheng Zhi Hao ◽  
Xiang Dong Zhang ◽  
Min Cai Li ◽  
Chuang Dong
Keyword(s):  
Electroless Plating ◽  
Electron Beam Irradiation ◽  
Xrd Analysis ◽  
High Current ◽  
X Ray Diffraction ◽  
X Ray ◽  
Pulsed Electron Beam ◽  
6063 Aluminum Alloy ◽  
Pre Treatment ◽  
Better Than

The surface irradiation of 6063 aluminum alloy by high current pulsed electron was conducted with the aim of replacing the complicated pre-treatment in the processes of electroless plating. To explore the microstructure changes, optical metallography, SEM (scanning electron microscope), XRD (X-ray diffraction) analyses were carried out, and the sliding tests were used for the detection of wear resistance. It was concluded that the HCPEB irradiation could replace the pre-treatment of aluminum substrate as required in conventional electroless plating with a decreased surface roughness of Ni-P alloy plating layer. The plates exhibited an amorphous microstructure as demonstrated by XRD analysis. The plates, produced with the routine of HCPEB irradiation, activation and electroless plating possess, also exhibited good quality, even better than that of conventional electroless plating technique.

Incorporation and Role of Nitrogen During Oxynitridation of Silicon Studied by Photoelectron Spectroscopy

1999 ◽  
Vol 567 ◽  
Author(s):  
Masayuki Suzuki ◽  
Yoji Saito
Keyword(s):  
Photoelectron Spectroscopy ◽  
High Vacuum ◽  
Oxide Films ◽  
Silicon Surfaces ◽  
Gaseous Mixtures ◽  
X Ray ◽  
Initial Stage ◽  
Thermal Stability Of

ABSTRACTWe tried direct oxynitridation of silicon surfaces by remote-plasma-exited nitrogen and oxygen gaseous mixtures at 700°C in a high vacuum. The oxynitrided surfaces were investigated with in-situ X-ray photoelectron spectroscopy. With increase of the oxynitridation time, the surface density of nitrogen gradually increases, but that of oxygen shows nearly saturation behavior after the rapid increase in the initial stage. We also annealed the grown oxynitride and oxide films to investigate the role of the contained nitrogen. The desorption rate of oxygen from the oxynitride films is much less than that from oxide films. We confirmed that nitrogen stabilizes the thermal stability of these oxynitride films.

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