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The practical application of aqueous zinc-ion batteries (ZIBs) indeed faces challenges primarily attributed to the inherent side reactions and dendrite growth associated with the Zn anode. In the present work, N-Methylmethanesulfonamide (NMS) is introduced to optimize the transfer, desolvation, and reduction of Zn 2+ , achieving highly stable and reversible Zn plating/stripping. The NMS molecule can substitute one H 2 O molecule in the solvation structure of hydrated Zn 2+ and be preferentially chemisorbed on the Zn surface to protect Zn anode against corrosion and hydrogen evolution reaction (HER), thereby suppressing byproducts formation. Additionally, a robust N-rich organic and inorganic (ZnS and ZnCO 3 ) hybrid solid electrolyte interphase is in situ generated on Zn anode due to the decomposition of NMS, resulting in enhanced Zn 2+ transport kinetics and uniform Zn 2+ deposition. Consequently, aqueous cells with the NMS achieve a long lifespan of 2300 h at 1 mA cm -2 and 1 mAh cm -2 , high cumulative plated capacity of 3.25 Ah cm -2 , and excellent reversibility with an average coulombic efficiency (CE) of 99.7 % over 800 cycles., (© 2024 Wiley-VCH GmbH.)

The adsorption layer system has shown great potential as a cost-effective and practical strategy for the recycling and management of excavated rocks containing potentially toxic elements (PTEs). Although this system has been employed in various civil engineering projects throughout Japan, its long-term performance to immobilize PTEs has rarely been investigated. This study aims to evaluate the effectiveness of the adsorption layer system applied in an actual road embankment approximately 11 years after construction. The embankment system is comprised of a layer of excavated arsenic (As)-bearing mudstone built on top of a bottom adsorption layer mixed with an iron (Fe)-based adsorbent. Collection of undisturbed sample was carried out by implementing borehole drilling surveys on the embankment. Batch leaching experiments using deionized water and hydrochloric acid were conducted to evaluate the water-soluble and acid-leachable concentrations of As, Fe, and other coexisting ions. The leaching of As from the mudstone layer was likely induced by As desorption from Fe-oxides/oxyhydroxides naturally present under alkaline conditions, including the oxidation of framboidal pyrite, which was identified as a potential source of As. This was supported by electron probe microanalyzer (EPMA) observations showing the presence of trace amounts of As in framboidal pyrite crystals. Arsenic leached from the mudstone layer was then immobilized by Fe oxyhydroxides found in the adsorption layer. Based on geochemical modeling and X-ray photoelectron spectroscopy (XPS) results, leached As predominantly existed as the negatively charged HAsO 4 oxyanion, which is readily sequestered by Fe oxyhydroxides. Moreover, the effectiveness of the adsorption layer was assessed and its lifetime was estimated, and the results revealed it still possessed enough capacity to adsorb As released from mudstone in the foreseeable future. This prediction utilized the maximum potential amount of As that could leach from the excavated rock layer with time.2- oxyanion, which is readily sequestered by Fe oxyhydroxides. Moreover, the effectiveness of the adsorption layer was assessed and its lifetime was estimated, and the results revealed it still possessed enough capacity to adsorb As released from mudstone in the foreseeable future. This prediction utilized the maximum potential amount of As that could leach from the excavated rock layer with time., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Ltd. All rights reserved.)

Context: Industrial production and humans cannot exist without energy, but the low efficiency of the heat transfer in the excessive use of energy is the most significant aspect of energy saving and emission reduction. Molecular dynamics simulation methods are devoted to simulate the heat transfer efficiency of a nanofluid system with different particle sizes, and the heat transfer enhancement mechanism of the nanofluid is simulated and studied from a microscopic perspective. The analysis showed that as nanoparticle size increases, the thermal conductivity of the Al-Ar nanofluid tends to decrease, but all of them are still higher than the thermal conductivity of the liquid argon system. According to the findings of the density and radial distribution function analyses, it can be seen that the microstructure of the system changes after putting solid nanoparticles to the original fluid. This alteration in the system's microstructure is the primary component responsible for the increased heat transfer efficiency of nanofluids., Methods: In this paper, based on the theory of molecular dynamics, the simulation calculations were mainly performed using LAMMPS software, which is a commonly used open source computational program in the field of MD simulation research. VMD is used for visualization and analysis. The Lennard-Jones potential function was used in the simulation to accurately describe the forces acting between the atoms., (© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

In this review, we highlight and discuss the effects of interfacial properties on the major mechanisms governing the aging of emulsions: flocculation, coalescence and Ostwald ripening. The process of emulsification is also addressed, as it is well recognized that the adsorption properties of emulsifiers play an important role on it. The consolidated background on these phenomena is briefly summarised based on selected literature, reporting relevant findings and results, and discussing some criticalities. The typical experimental approaches adopted to investigate the above effects are also summarised, underlining in particular the role of adsorption at the droplet interface. Attention is paid to different types of surface-active species involved with emulsion production, including solid particles. The latter being of increasing interest in a wide variety of emulsions-related products and technologies in various fields. The possibility to stop the long term aging caused by Ostwald ripening in emulsions is also discussed, quantifying under which conditions it may occur in practice., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper. The authors declare the following financial interests/personal relationships which may be considered as potential competing interests:, (Copyright © 2020. Published by Elsevier B.V.)

Enhancement in dispersion of polycarboxylate superplasticizer (PCE) could be obtained by incorporating retarders in normal concrete. The generally believed reason was that the consumption of free water and polymer at the beginning was reduced by retarding cement hydration. This theory could not convincingly explain why sodium hexametaphosphate (SHMP) was able to promote the dispersion capacity of PCE, while trisodium phosphate (TSP) could not, despite that both TSP and SHMP could obviously retard the cement hydration. The adsorption behavior of PCE and phosphate was investigated and the mechanism was analyzed in order to gain deeper understanding. The results showed that TSP and SHMP delayed the cement hydration, impeded adsorption process of PCE, and increased thickness of adsorption layer. It was interesting that TSP reduced the dispersion, but SHMP enhanced. The reason for this contradiction was due to the difference in composition of adsorption layer. In the PCE-TSP system, this layer was composed of the precipitates (formed by TSP and Ca 2+ ) and the invalided PCE (caused by these precipitates in the immediate vicinity of the cement grains); the invalided PCE was due to the decrease of PCE dispersion. In the PCE-SHMP system, "Inner-phosphate (multi-layers) + Outer-PCE (single layer)" structure was formed to make the PCE work more effective, hence enhancing the dispersion. These results were expected to be useful for the design of highly efficient dispersants.

The adsorption behavior of γ -aminopropyl trimethoxysilane ( γ -APS) on copper foil is investigated by using X-ray photoelectron spectroscopy (XPS). Copper foil is immersed in a diluted aqueous solution of γ -APS and dried in air. It is found that γ -APS is adsorbed onto the surface almost without hydrolysis. Further, the depth profile by XPS analysis shows that γ-APS is not hydrolyzed even in the inside layer. In order to obtain hydrolyzed γ-APS on the copper foil surface, the foil is freeze-dried as immersed in a diluted aqueous solution of γ -APS. A hydrolyzed form of γ -APS is found on the top surface. Further, the presence of a powder is confirmed in the bottom of the flask at the end of the freeze-dry experiment. XPS analysis shows the powder is a linear polymer and produced from the silane coupling agent., (© The Author(s) 2009.)