Institutional Repository of Institute of Process Engineering, CAS (IPE-IR)
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CFD-DEM simulations of wet particles fluidization with a new evolution model for liquid bridge
A new model for liquid-bridge evolution with consideration of particle dynamics, is proposed to improve Computational Fluid Dynamics-Discrete Element Method (CFD-DEM) simulations of wet particles fluidization under high liquid loading and viscosity. A liquid bridge is allowed to form and remains stable only when the normal relative velocity of two particles is lower than a critical value v(nc). A large v(nc) leads to an increase of liquid-bridge or cohesive force. The model can be reduced to the conventional liquid-bridge model in literature when v(nc) = 0 or infinity. With the new model, the prediction of bubble properties including bubble center, aspect ratio, and volume agrees well with the experimental data in literature. In particular, under high liquid loading, bubble disintegration due to particle agglomerating is reasonably captured. The simulations demonstrate the advantage of the new model that can extend the liquid-bridge models and CFD-DEM for high liquid loading and viscosity
High recycling Fe3O4-CdTe nanocomposites for the detection of organophosphorothioate pesticide chlorpyrifos
To alleviate the secondary contamination of our environment when using quantum dots (QDs) to detect the organophosphorothioate pesticides (OPPs), we herein report a strategy to assemble magnetic Fe3O4 nanoparticles and luminescent CdTe quantum dots (QDs) into a composite nanosystem, which possesses both the magnetic property of Fe3O4 nanoparticles and the luminescent character of CdTe QDs, for the detection of chlorpyrifos, one of the typical OPPs. This strategy involves the isolated synthesis of magnetic Fe3O4 nanoparticles with positive charges and luminescent CdTe QDs with negative charges, and their subsequent assembly by electrostatic interaction. The as-prepared Fe3O4-CdTe nanocomposites have a detection limit as low as 10 ppb for chlorpyrifos, and are also selective for the OPPs with a phosphorothioate moiety (P = S bond). In specific, the Fe3O4-CdTe nanocomposites can be conveniently harvested by a normal magnet, and the recycling rate for both Cd and Fe determined by inductively coupled plasma atomic emission spectroscopy (ICP-AES) is higher than 96%, showing great potential in alleviating the Cd pollution on the environment. (C) 2020 Institute of Process Engineering, Chinese Academy of Sciences. Publishing services by Elsevier B.V. on behalf of KeAi Communications Co., Ltd
Science and Technology Innovation Committee of Shenzhen Municipality[JSGG20191129144225464]
Interfacial engineering of transition-metal sulfides heterostructures with built-in electric-field effects for enhanced oxygen evolution reaction
Developing highly efficient, durable, and non-noble electrocatalysts for the sluggish anodic oxygen evolution reaction (OER) is the pivotal for meeting the practical demand in water splitting. However, the current transition-metal electrocatalysts still suffer from low activity and durability on account of poor interfacial reaction kinetics. In this work, a facile solid-state synthesis strategy is developed to construct transition-metal sulfides heterostructures (denoted as MS2/NiS2, M = Mo or W) for boosting OER electrocatalysis. As a result, MoS2/NiS2 and WS2/NiS2 show lower overpotentials of 300 mV and 320 mV to achieve the current density of 10 mA.cm(-2), and smaller Tafel slopes of 60 mV.dec(-1) and 83 mV-dec(-1) in 1 mol.L-1 KOH, respectively, in comparison with the single MoS2, WS2, NiS2, as well as even the benchmark RuO2. The experiments reveal that the designed heterostructures have strong electronic interactions and spontaneously develop a built-in electric field at the heterointerface with uneven charge distribution based on the difference of band structures, which promote interfacial charge transfer, improve absorptivity of OH , and modulate the energy level more comparable to the OER. Thus, the designed transition-metal sulfides heterostructures exhibit a remarkably high electrocatalytic activity for OER. This study provides a simple strategy to manipulate the heterostructure interface via an energy level engineering method for OER and can be extended to fabricate other heterostructures for various energy-related applications. (C) 2021 The Chemical Industry and Engineering Society of China, and Chemical Industry Press Co., Ltd. All rights reserved
A novel strontium carbonate/strontium sulfate/strontium titanate composite with core shell structure for photocatalytic degradation of dyes
A core-shell structure SrSO4-SrCO3 (SSO-SCO) composite was synthesized with strontium titanate and ammonium carbonate. The SrTiO3-SrSO4-SrCO3 (TSC) composite with core-shell structure was obtained by adding strontium titanate into the mixture through hydrothermal method. The morphology, elemental composition and crystallinity of the catalyst were characterized by SEM, EDS, TEM and XRD analyses. The TSC composite exhibited excellent photocatalytic performance for the degradation of methylene blue dyes compared to the SrTiO3. The high catalytic efficiency was due to synergistic effect of the increased light harvesting and efficient transport of photogenerated electron and hole pairs in composites based on the results of UV-vis and PL and transient photocurrent response tests. Furthermore, ESR spectra showed that center dot OH radicals and hole radicals were the main active species contributing to the excellent performance. Based on the photocatalytic results and ESR spectra, a photocatalytic mechanism for MB degradation was proposed
Research Project of Shanxi Provincial Department of Science and Technology[202003D311001]
Transferring Liquid Metal to form a Hybrid Solid Electrolyte via a Wettability-Tuning Technology for Lithium-Metal Anodes
Integrating solid-state electrolyte (SSE) into Li-metal anodes has demonstrated great promise to unleash the high energy density of rechargeable Li-metal batteries. However, fabricating a highly cyclable SSE/Li-metal anode remains a major challenge because the densification of the SSE is usually incompatible with the reactive Li metal. Here, a liquid-metal-derived hybrid solid electrolyte (HSE) is proposed, and a facile transfer technology to construct an artificial HSE on the Li metal is reported. By tuning the wettability of the transfer substrates, electron- and ion-conductive liquid metal is sandwiched between electron-insulating and ion-conductive LiF and oxides to form the HSE. The transfer technology renders the HSE continuous, dense, and uniform. The HSE, having high ion transport, electron shut-off, and mechanical strength, makes the composite anode deliver excellent cyclability for over 4000 h at 0.5 mA cm(-2) and 1 mAh cm(-2) in a symmetrical cell. When pairing with LiFePO4 and sulfur cathodes, the HSE-coated Li metal dramatically enhances the performance of full cells. Therefore, this work demonstrates that tuning the interfacial wetting properties provides an alternate approach to build a robust solid electrolyte, which enables highly efficient Li-metal anodes