Reaction Mechanism of In-situ Carbon in Hematite Ore Pellet during Induration

Author(s):  
Ammasi Ayyandurai ◽  
Jagannath Pal
2021 ◽  
Vol 13 (1) ◽  
Author(s):  
Shen Wang ◽  
Hongbo Xu ◽  
Tingting Hao ◽  
Peiyuan Wang ◽  
Xiang Zhang ◽  
...  

AbstractElectrochromic supercapacitors (ESCs) are appealing for smart electronic device applications due to their advantages of dual-function integration. Unfortunately, the synchronous dual-function evaluation and the essential reaction mechanism are ambiguous. Herein, we constructed a 3D WO3-x nanowire networks/fluorine-doped tin oxide (WO3-x NWNs/FTO) bifunctional electrode for ESCs by a solvothermal self-crystal seeding method. The synchronous correspondence relationship between the optical and electrochemical performances of the WO3-x NWNs/FTO electrode was explored using an operando spectra-electrochemical characterization method. It reveals an excellent areal capacity of 57.57 mF cm−2 with a high corresponding optical modulation (ΔT) of 85.05% and high optical-electrochemical cycling stability. Furthermore, the synergistic reaction mechanism between the Al3+ ion intercalation behavior and the surface pseudocapacitance reaction during electrochemical cycling is revealed utilizing in situ X-ray diffraction. Based on these results, an ESC device was constructed by pairing WO3-x/FTO as the cathode with V2O5 nanoflowers/FTO (V2O5 NFs/FTO) as the anode, which simultaneously deliver high capacity and large optical modulation. Moreover, the energy storage level of the ESC device could be visually monitored by rapid and reversible color transitions in real time. This work provides a promising pathway to developing multi-functional integrated smart supercapacitors.


2011 ◽  
Vol 257 (7) ◽  
pp. 2707-2711 ◽  
Author(s):  
S. Bruijn ◽  
R.W.E. van de Kruijs ◽  
A.E. Yakshin ◽  
F. Bijkerk

2016 ◽  
Vol 12 ◽  
pp. 1421-1427 ◽  
Author(s):  
Grzegorz Mlostoń ◽  
Róża Hamera-Fałdyga ◽  
Anthony Linden ◽  
Heinz Heimgartner
Keyword(s):  

Ferrocenyl hetaryl thioketones react smoothly with in situ generated thiocarbonyl S-methanides to give 1,3-dithiolanes. In the case of aromatic S-methanides, the sterically more crowded 4,4,5,5-tetrasubstituted 1,3-dithiolanes (2-CH2 isomers) were formed as sole products. The reactions with cycloaliphatic S-methanides led to mixtures of 2-CH2 and 5-CH2 isomers with the major component being the sterically more crowded 2-CH2 isomers. The preferred formation of the latter products is explained by the assumption that the formal [3 + 2]-cycloadducts were formed via a stepwise reaction mechanism with a stabilized 1,5-diradical as a key intermediate. The complete change of the reaction mechanism toward the concerted [3 + 2]-cycloaddition was observed in the reaction of a sterically crowded cycloaliphatic thiocarbonyl ylide with ferrocenyl methyl thioketone.


Fuel ◽  
2019 ◽  
Vol 239 ◽  
pp. 162-172 ◽  
Author(s):  
Guoliang Li ◽  
Shuxiao Wang ◽  
Qingru Wu ◽  
Junhua Li ◽  
Xiaoqing You ◽  
...  

2019 ◽  
Vol 297 ◽  
pp. 46-54 ◽  
Author(s):  
Libing Yao ◽  
Meng Nie ◽  
Chongyang Zhu ◽  
Ran Cai ◽  
Weiwei Xia ◽  
...  

2018 ◽  
Vol 763 ◽  
pp. 349-354 ◽  
Author(s):  
Xiaopeng Cheng ◽  
Yonghe Li ◽  
Huifeng Shi ◽  
Junxia Lu ◽  
Yuefei Zhang

2017 ◽  
Vol 7 (3) ◽  
pp. 658-667 ◽  
Author(s):  
Xin Geng ◽  
Wentao Li ◽  
Feng Xiao ◽  
Dongsheng Wang ◽  
Lian Yang

Scheme of the visible light-Fenton-like catalytic reaction mechanism.


Minerals ◽  
2019 ◽  
Vol 9 (4) ◽  
pp. 244 ◽  
Author(s):  
Keyser ◽  
Ciobanu ◽  
Cook ◽  
Feltus ◽  
Johnson ◽  
...  

Zirconium is an element of considerable petrogenetic significance but is rarely found in hematite at concentrations higher than a few parts-per-million (ppm). Coarse-grained hematite ore from the metamorphosed Peculiar Knob iron deposit, South Australia, contains anomalous concentrations of Zr and has been investigated using microanalytical techniques that can bridge the micron- to nanoscales to understand the distribution of Zr in the ore. Hematite displays textures attributable to annealing under conditions of high-grade metamorphism, deformation twins (r~85˚ to hematite elongation), relict magnetite and fields of sub-micron-wide inclusions of baddeleyite as conjugate needles with orientation at ~110˚/70˚. Skeletal and granoblastic zircon, containing only a few ppm U, are both present interstitial to hematite. Using laser-ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) spot analysis and mapping, the concentration of Zr in hematite is determined to be ~260 ppm on average (up to 680 ppm). The Zr content is, however, directly attributable to nm-scale inclusions of baddeleyite pervasively distributed throughout the hematite rather than Zr in solid solution. Distinction between nm-scale inclusions and lattice-bound trace element substitutions cannot be made from LA-ICP-MS data alone and requires nanoscale characterization. Scandium-rich (up to 0.18 wt. % Sc2O3) cores in zircon are documented by microprobe analysis and mapping. Using high-angle annular dark field scanning transmission electron microscopy imaging (HAADF-STEM) and energy-dispersive spectrometry STEM mapping of foils prepared in-situ by focused ion beam methods, we identify [011]baddeleyite epitaxially intergrown with [22.1]hematite. Lattice vectors at 84–86˚ underpinning the epitaxial intergrowth orientation correspond to directions of r-twins but not to the orientation of the needles, which display a ~15˚ misfit. This is attributable to directions of trellis exsolutions in a precursor titanomagnetite. U–Pb dating of zircon gives a 206Pb/238U weighted mean age of 1741 ± 49 Ma (sensitive high-resolution ion microprobe U–Pb method). Based on the findings presented here, detrital titanomagnetite from erosion of mafic rocks is considered the most likely source for Zr, Ti, Cr and Sc. Whether such detrital horizons accumulated in a basin with chemical precipitation of Fe-minerals (banded iron formation) is debatable, but such Fe-rich sediments clearly included detrital horizons. Martitization during the diagenesis-supergene enrichment cycle was followed by high-grade metamorphism during the ~1.73–1.69 Ga Kimban Orogeny during which martite recrystallized as granoblastic hematite. Later interaction with hydrothermal fluids associated with ~1.6 Ga Hiltaba-granitoids led to W, Sn and Sb enrichment in the hematite. By reconstructing the evolution of the massive orebody at Peculiar Knob, we show how application of complimentary advanced microanalytical techniques, in-situ and on the same material but at different scales, provides critical constraints on ore-forming processes.


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