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Elastic modulus plays a key role in the application of porous metallic materials. However, to the best of our knowledge, few attempts have been made to model the simultaneous dependence of elastic modulus on temperature and porosity for metallic materials. The present article contributes to a rational temperature-porosity-dependent elastic modulus model for metallic materials with all parameters having definite physical significance. The model can well predict the elastic moduli of porous metallic materials, from extremely low temperature to ultrahigh temperature, and from dense material to about 0.9 porosity, with reference to an easy-to-access elastic modulus. In a special case, when intrinsic elastic modulus [M] = 2 and critical porosity P C = 1, a phenomenological parameter-free predictive model can be obtained. The model can be applied when the matrix Poisson ratio is 0.1 < v < 0.4 for Young’s modulus and 0.17 < v < 0.27 for shear modulus, which covers most metallic porous materials.

Amongst various Fenton-like single-atom catalysts (SACs), the zinc (Zn)-related SACs have been barely reported due to the fully occupied 3d 10 configuration of Zn 2+ being inactive for the Fenton-like reaction. Herein, the inert element Zn is turned into an active single-atom catalyst (SA-Zn-NC) for Fenton-like chemistry by forming an atomic Zn-N 4 coordination structure. The SA-Zn-NC shows admirable Fenton-like activity in organic pollutant remediation, including self-oxidation and catalytic degradation by superoxide radical (O 2 ⋅ - ) and singlet oxygen ( 1 O 2 ). Experimental and theoretical results unveiled that the single-atomic Zn-N 4 site with electron acquisition can transfer electrons donated by electron-rich pollutants and low-concentration PMS toward dissolved oxygen (DO) to actuate DO reduction into O 2 ⋅ - and successive conversion into 1 O 2 . This work inspires an exploration of efficient and stable Fenton-like SACs for sustainable and resource-saving environmental applications., (© 2023 Wiley-VCH GmbH.)

Achieving satisfactory organic pollutant oxidation with a low concentration of peroxymonosulfate (PMS) is vital for persulfate-involved advanced oxidation processes to reduce resource consumption and avoid excessive sulfate anion (SO 4 2- ) production. Herein, efficient conversion of dissolved oxygen (DO) over single-atomic Fe-N 3 O 1 sites anchored on carbon nitride for efficient contaminant degradation is fulfilled, triggered by a low concentration of PMS (0.2 mm). Experimental and theoretical results reveal that the preferentially adsorbed PMS onto atomic Fe-N 3 O 1 center can deliver electrons toward the single Fe atom to increase its electron density to trigger DO reduction into superoxide radical (O 2 • - ) and successive transformation into singlet oxygen ( 1 O 2 ), which is quite different from the conventional PMS activation process mostly depending on PMS itself function for reactive oxygen species generation. On the other hand, PMS with high concentration could occupy active Fe-N 3 O 1 sites to hamper DO conversion and further produce massive SO 4 2- . A couple of -Fe-CN 0.05 -and slight PMS is effective for actual kitchen wastewater remediation and long-term bisphenol A degradation. This work elucidates the triggering role of low-concentration PMS in DO conversion over a single-atom Fe catalyst, which can inspire the development of resource-saving, cost-effective, and environmentally-friendly catalytic oxidation systems for environmental restoration., (© 2022 Wiley-VCH GmbH.)

The effects of biological activated carbon treatment using Fe 2 O 3 modified coconut shell-based activated carbon (Fe/CAC) were investigated on the occurrence of opportunistic pathogens (OPs) and formation of disinfection by-products (DBPs) in simulated drinking water distribution systems (DWDSs) with unmodified CAC as a reference. In the effluent of annular reactor (AR) with Fe/CAC, the OPs growth and DBPs formation were inhibited greatly. Based on the differential pulse voltammetry and dehydrogenase activity tests, it was verified that extracellular electron transfer was enhanced in the attached biofilms of Fe/CAC, hence improving the microbial metabolic activity and biological removal of organic matter especially DBPs precursors. Meanwhile, the extracellular polymeric substances (EPS) on the surface of Fe/CAC exhibited stronger viscosity, higher flocculating efficiency and better mechanical stability, avoiding bacteria or small-scale biofilms falling off into the water. Consequently, the microbial biomass and EPS substances amount decreased markedly in the effluent of Fe/CAC filter. More importantly, Fe/CAC did significantly enhance the shaping role on microbial community of downstream DWDSs, continuously excluding OPs advantage and inhibiting EPS production. The weakening of EPS in DWDSs resulted in decrease of microbial chlorine-resistance ability and EPS-derived DBPs precursors supply. Therefore, the deterioration of water quality in DWDSs was inhibited greatly, sustainably maintaining the safety of tap water. Our findings indicated that optimizing biological activated carbon treatment by interface modification is a promising method for improving water quality in DWDSs., 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 © 2020 Elsevier Ltd. All rights reserved.)

The development of highly efficient and stable visible-light-responsive photoanode materials is essential for practical photoelectrocatalytic (PEC) applications. In this work, a novel method was proposed to enhance the PEC efficiency and stability of WO3 photoanodes by the facile in situ growth of TiO2 branch overlayers on WO3 nanoplates (TWNP) based on the lattice match between monoclinic WO3 and anatase TiO2. The WO3 nanoplates (WNP) with a fluted body and a thickness of 160 nm were first prepared on tungsten foil by a hydrothermal method. Then, numerous 001-oriented anatase TiO2 branches were directly grown in situ on the WNP with an average thickness of 50 nm and a length of 35 ± 5 nm. TWNP exhibited a photocurrent of ∼2.37 mA cm-2, which is 157% of that of WNP, and showed no obvious decay over 100 h continuous testing, compared to only 11.8% that remained for WNP. During the PEC degradation of phenol, the rate constant was 0.322 h-1 for TWNP while it was only 0.131 h-1 for WNP, and the activity of TWNP remained at 97.2% after 10 repeat tests compared to only 67.4% for WNP. According to the transient photovoltage and transient photocurrent measurements, these improvements can be attributed to the TiO2 branches which enhanced the charge separation efficiency and surface reaction kinetics, and hindered the inactivation of TWNP by providing an atomic-level protective cover. Overall, the in situ wet chemical growth of the TiO2 branches is a meaningful way to overcome WO3's drawbacks, i.e., sluggish surface reaction kinetics, rapid charge recombination and gradual loss of photoactivity, to improve the PEC activity and stability of WO3 photoanodes.