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This study conducts low-vacuum sulfidation to form a sulfidation layer on the serpentinite-derived magnesium iron silicate, thereby enhancing its electrochemical properties. Results show (Mg,Fe)2SiO4 calcined at 900 °C has the best crystallinity, and the cubic FeS2 is synthesized on the surface of the orthorhombic magnesium iron silicate (MFS). Two distinct charge plateaus can be distinguished during the first charge process, and the discharge capacities increased significantly. This study confirms that the surface FeS2 layer provides extra ion pathways, allowing more lithium/magnesium ions to be extracted and inserted in the serpentinite-derived magnesium iron silicate. Accordingly, the serpentinite electrode boasts straightforward exploitation with low-cost advantages and potential. [ABSTRACT FROM AUTHOR]

Utilizing iron silicate copper slag as supplementary cementitious material (SCM) is a means to improve resource efficiency and lower the carbon dioxide emissions from cement production. Despite multiple studies on the performance of these slags in SCM applications, the variations in cooling procedure, grinding, and methods for evaluating reactivity limit the ability to assess the influence of chemical composition on reactivity from the literature data. In this study, a methodology was developed to synthesize iron silicate slags, which were then evaluated for their inherent reactivity using the R3 calorimeter-based experiments. The results demonstrated that laboratory-scale granulation produced the same reactivity as industrially granulated slag. Furthermore, a synthesized triplicate sample showed high repeatability. Based on these two aspects, this method can be used to systematically study the influence of chemical composition on the inherent reactivity of iron silicate slags while producing results that are directly translatable to industrial slags. [ABSTRACT FROM AUTHOR]

Iron–manganese silicate (IMS) was synthesized by chemical coprecipitation and used as a catalyst for ozonating acrylic acid (AA) in semicontinuous flow mode. The Fe-O-Mn bond, Fe-Si, and Mn-Si binary oxide were formed in IMS on the basis of the results of XRD, FTIR, and XPS analysis. The removal efficiency of AA was highest in the IMS catalytic ozonation processes (98.9% in 15 min) compared with ozonation alone (62.7%), iron silicate (IS) catalytic ozonation (95.6%), and manganese silicate catalytic ozonation (94.8%). Meanwhile, the removal efficiencies of total organic carbon (TOC) were also improved in the IMS catalytic ozonation processes. The IMS showed high stability and ozone utilization. Additionally, H2O2 was formed in the process of IMS catalytic ozonation. Electron paramagnetic resonance (EPR) analysis and radical scavenger experiments confirmed that hydroxyl radicals (•OH) were the dominant oxidants. Cl−, HCO3−, PO43−, Ca2+, and Mg2+ in aqueous solution could adversely affect AA degradation. In the IMS catalytic ozonation of AA, the surface hydroxyl groups and Lewis acid sites played an important role. [ABSTRACT FROM AUTHOR]

The zinc in the fayalite slag of copper smelters, in which Zn-containing raw materials are used, is mainly found to be in oxidic phases, such as glassy iron silicate. During the slag water granulation process, the molten slag is heated, whereby the granulated slag achieves varying granulation temperatures. Therefore, in this study, we aimed to characterize and assess the leaching behavior of a synthesized Fe-saturated (FeX,Zn(1−X))2SiO4 system to understand the dependance of the zinc leaching behavior on the parameters of the ZnO content (1–10 wt.%) and granulation temperature (1300 or 1400 °C). It was found that the Zn leaching increased with the increasing Zn content and granulation temperature, using both batch and static pH leaching methods. Zn leaching was further increased at pH 5 using diluted nitric acid under oxidation conditions. Among the oxides in the samples—fayalite, spinel, and glass—glass was found to contribute to Zn leaching, owing to its weathering during pH-titration. [ABSTRACT FROM AUTHOR]

The application of fluxed pellets in iron making industry has attracted considerable attention because of the better metallurgical properties than acid pellets and environmental friendliness compared to sinters. However, fluxed pellets with different binary basicity (CaO/SiO2) exhibited significant differences in phase composition, microstructure and consolidation mechanism. These differences mainly stemmed from the influence of calcium-containing substances in fluxed pellets. Herein, the theoretical investigation discovered the calcium-containing substances from fluxed pellets, including calcium iron silicate, calcium silicate and complex calcium ferrite (SFCA), which determined the properties of fluxed pellets. Microstructure analysis revealed that the calcium-containing substances filled between hematite particles were used as a binding phase to assist in pellets' consolidation. Furthermore, the calcium-containing binding phase formed in the low-basicity (0.4–1.0) pellets was mainly composed of the calcium iron silicate glassy phase, while the binding phase of the high-basicity (1.0–1.2) pellets was dominated by SFCA belonging to SiO2-Fe2O3-CaO-Al2O3 multivariate system. In comparison, SFCA exhibited better crystallinity and reducibility than calcium iron silicate. Within the roasting temperature range of 1200–1250 °C, the increase of basicity contributed to the fluxed pellets obtaining better strength. To sum up, fluxed pellets with SFCA as the main calcium-containing binding phase can be obtained by increasing the basicity above 1.0–1.2, which was imperative for further improving the physical and metallurgical properties of fluxed pellets. [ABSTRACT FROM AUTHOR]

High-capacity and high-voltage cathode materials are required to meet the increasing demand for energy density in Li ion batteries. Lithium iron silicate (Li2FeSiO4) is a cathode material with a high theoretical capacity of 331 mAh·g−1. However, its poor conductivity and low Li ion diffusion coefficient result in poor capability, hindering practical applications. Morphology has an important influence on the properties of materials, and nanomaterials with hollow structures are widely used in electrochemical devices. Herein, we report a novel hollow hemispherical Li2FeSiO4 synthesized by a template-free hydrothermal method with the addition of ascorbic acid. The hollow hemispherical Li2FeSiO4 consisted of finer particles with a shell thickness of about 80 nm. After carbon coating, the composite was applied as the cathode in Li ion batteries. As a result, the hollow hemispherical Li2FeSiO4/C exhibited a discharge capacity as high as 192 mAh·g−1 at 0.2 C, and the average capacities were 134.5, 115.5 and 93.4 mAh·g−1 at 0.5, 1 and 2 C, respectively. In addition, the capacity increased in the first few cycles and then decayed with further cycling, showing a warm-up like behavior, and after 160 cycles the capacities maintained 114.2, 101.6 and 79.3 mAh·g−1 at 0.5, 1 and 2 C, respectively. Such a method of adding ascorbic acid in the hydrothermal reaction can effectively synthesize hollow hemispherical Li2FeSiO4 with the enhanced electrochemical performance. [ABSTRACT FROM AUTHOR]

Bioleaching of olivine, a natural nickel-containing magnesium-iron-silicate, was conducted by applying chemoorganotrophic bacteria and fungi. The tested fungus, Aspergillus niger, leached substantially more nickel from olivine than the tested bacterium, Paenibacillus mucilaginosus. Aspergillus niger also outperformed two other fungal species: Humicola grisae and Penicillium chrysogenum. Contrary to traditional acid leaching, the microorganisms leached nickel preferentially over magnesium and iron. An average selectivity factor of 2.2 was achieved for nickel compared to iron. The impact of ultrasonic conditioning on bioleaching was also tested, and it was found to substantially increase nickel extraction by A. niger. This is credited to an enhancement in the fungal growth rate, to the promotion of particle degradation, and to the detachment of the stagnant biofilm around the particles. Furthermore, ultrasonic conditioning enhanced the selectivity of A. niger for nickel over iron to a value of 3.5. Pre-carbonating the olivine mineral, to enhance mineral liberation and change metal speciation, was also attempted, but did not result in improvement as a consequence of the mild pH of chemoorganotrophic bioleaching. [ABSTRACT FROM AUTHOR]

Copper in discarded slag decreases the profits and copper recovery during the pyrometallurgical extraction processes. The copper losses to slag can be reduced by using a settling furnace, in which mechanically entrained copper droplets separate from the slag under the action of gravity. The settling rate of entrained droplets can be increased by modifying the slag composition and, thus, the slag properties, which are known to influence the settling rate. The knowledge of industrial CaO slag modification in a reduced iron silicate slag with a Fe/SiO2 ratio close to unity is limited. An industrial trial was thus conducted in an electric settling furnace, where the slag had been pretreated in a fuming furnace, to investigate the effect of CaO slag modification on the final slag copper content. Slag samples were collected from the ingoing and outgoing slag and from within the furnace of batches modified with CaO up to about 16 wt %. The trial was evaluated by comparing the final slag copper content and the copper recovery in the settling furnace. The results indicate that the settling becomes more efficient with the CaO modification as the final slag copper content decreased with increasing CaO content. [ABSTRACT FROM AUTHOR]

During the pyrometallurgical extraction of copper, a significant fraction of this metal is lost with discard slag, which decreases profits and overall copper recovery. These copper losses can be reduced by using a settling furnace, in which suspended droplets containing copper separate from slag under the influence of gravity. An industrial trial was conducted in a settling furnace to increase the knowledge of the effect of temperature and settling time on the copper content of slag, and thus enhance the settling process to increase copper recovery. Slag samples were collected from four sample points: the ingoing and outgoing slag stream, within the furnace during settling, and the granulated slag. The chemical composition of the slag samples was analyzed and compared between batches with different temperatures and settling times. The appearance of copper and its associated phases were analyzed using a scanning electron microscope with an energy-dispersive X-ray spectroscopy detector (SEM-EDS). The results indicated that the outgoing slag copper content increased with an increase in temperature, and it was also concluded to be influenced by the attachment of copper to spinels and gas bubbles. The results indicate that regulating the settling furnace temperature to a lower interval could increase copper recovery. [ABSTRACT FROM AUTHOR]

This study is a multi-technique investigation of the Paris carbonaceous chondrite directly applied on two selected 500 × 500 µm² areas of a millimetric fragment, without any chemical extraction. By mapping the partial hydration of the amorphous silicate phase dominating the meteorite sample matrix, infrared spectroscopy gave an interesting glimpse into the way the fluid may have circulated into the sample and partially altered it. The TOF-SIMS in-situ analysis allowed the studying and mapping of the wide diversity of chemical moieties composing the meteorite organic content. The results of the combined techniques show that at the micron scale, the organic matter was always spatially associated with the fine-grained and partially-hydrated amorphous silicates and to the presence of iron in different chemical states. These systematic associations, illustrated in previous studies of other carbonaceous chondrites, were further supported by the identification by TOF-SIMS of cyanide and/or cyanate salts that could be direct remnants of precursor ices that accreted with dust during the parent body formation, and by the detection of different metal-containing large organic ions. Finally, the results obtained emphasized the importance of studying the specific interactions taking place between organic and mineral phases in the chondrite matrix, in order to investigate their role in the evolution story of primitive organic matter in meteorite parent bodies. [ABSTRACT FROM AUTHOR]