Publications by authors named "Huanggen Yang"

The conveniently recoverable piezocatalyst with self-floating and stable performance has drawn wide attention. Herein, MoS was anchored on 1-cm-square eucalyptus wood blocks via a facile hydrothermal/solvothermal process to fabricate two floating piezocatalysts, i.e.

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A unique combination of cotton fabric (CF) with a mixture of EDTA and APTES FeO magnetic particles was developed and utilized for the first time as an adsorbent for removing pollutants from wastewater. Initially, FeO was synthesized using the co-precipitation method. Further, the surface of FeO was modified by introducing amino functional groups through a reaction with APTES, resulting in FeO-NH.

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The presence of pollutants in drinking water has become a significant concern recently. Various substances, including activated carbon, membranes, biochar, etc., are used to remove these pollutants.

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Persulfate non-radical oxidation have excellent catalytic capability for degrading specific contaminants in complicated water environments. Nevertheless, the preparation of high-performance activators and their application in actual water treatment in continuous flow mode are still scarce and unsatisfactory. In this work, copper-, manganese-, and copper/manganese-doped ceramsites (Cu-C, Mn-C and Cu/Mn-C), successfully fabricated through a facile impregnation-calcination approach, were characterized and evaluated for their performance to activate potassium peroxydisulfate (PDS) and degrade oxytetracycline (OTC) under different pH, ceramsite dosages, and PDS dosages.

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In this work, the synergistic inhibitions of tungstate (WO) and molybdate (MoO) anions, including role and mechanism, on the initiation of pitting corrosion (PC) for Q235 carbon steel in chloride (Cl) solution were investigated with electrochemical and surface techniques. The pitting potential (E) of the Q235 carbon steel in WO + MoO + Cl solution was more positive than that in WO + Cl or MoO + Cl solution; at each E, both peak potential and affected region of active pitting sites in WO + MoO + Cl solution were smaller than those in WO + Cl or MoO + Cl solution. WO and MoO showed a synergistic role to inhibit the PC initiation of the Q235 carbon steel in Cl solution, whose mechanism was mainly attributed to the influences of two anions on passive film.

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The exponentially increased use of gold nanoclusters in diagnosis and treatment has raised serious concern about their potential threat to living organisms. However, the mechanisms of toxicity of gold nanoclusters and remain poorly understood. In this work, comparative toxicity studies, including biodistribution and excretion, were carried out with mildly and chemically synthesized ultra-small L-histidine-protected and bovine serum albumin (BSA)-protected gold nanoclusters in an all-aqueous process.

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Commercial TiO supported 0.20 wt% Pt catalyst is obtained via the molten salt method, and both Pt nanoparticles and single atom Pt sites are observed. It exhibits high catalytic performance for toluene oxidation, with T and T being 173 and 183 °C, respectively.

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Using a mixture of NaNO3 and NaF as molten salt and MnSO4 and AgNO3 as metal precursors, 0.13 wt % Ag/Mn2O3 nanowires (0.13Ag/Mn2O3-ms) were fabricated after calcination at 420 °C for 2 h.

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Three-dimensionally ordered macroporous (3DOM) Mn2O3 and its supported gold (xAu/3DOM Mn2O3, x=1.9-7.5wt%) nanocatalysts were prepared using the polymethyl methacrylate-templating and polyvinyl alcohol-protected reduction methods, respectively.

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Porous cube-aggregated monodisperse Co3O4 microspheres and their supported gold (xAu/Co3O4 microsphere, x=1.6-7.4 wt %) nanoparticles (NPs) were fabricated using the glycerol-assisted solvothermal and polyvinyl alcohol-protected reduction methods.

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Three-dimensionally ordered macroporous Co3O4 (3DOM Co3O4) and its supported gold (xAu/3DOM Co3O4, x = 1.1-8.4 wt%) nanocatalysts were prepared using the polymethyl methacrylate-templating and bubble-assisted polyvinyl alcohol-protected reduction methods, respectively.

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Uniform hollow spherical rhombohedral LaMO3 and solid spherical cubic MOx (M = Mn and Co) NPs were fabricated using the PMMA-templating strategy. Hollow spherical LaMO3 and solid spherical MOx NPs possessed surface areas of 21-33 and 21-24 m(2)/g, respectively. There were larger amounts of surface-adsorbed oxygen species and better low-temperature reducibility on/of the hollow spherical LaMO3 samples than on/of the solid spherical MOx samples.

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