Core-Shell-Like Structured Co3O4@SiO2 Catalyst for Highly Efficient Catalytic Elimination of Ozone

Co3O4 is an environmental catalyst that can effectively decompose ozone, but is strongly affected by water vapor. In this study, Co3O4@SiO2 catalysts with a core-shell-like structure were synthesized following the hydrothermal method. At 60% relative humidity and a space velocity of 720,000 h−1, the prepared Co3O4@SiO2 obtained 95% ozone decomposition for 40 ppm ozone after 6 h, which far outperformed that of the 25wt% Co3O4/SiO2 catalysts. The superiority of Co3O4@SiO2 is ascribed to its core@shell structure, in which Co3O4 is wrapped inside the SiO2 shell structure to avoid air exposure. This research provides important guidance for the high humidity resistance of catalysts for ozone decomposition.

Utilization of Waste Clam Shell as Cost-Effective Catalyst for Heterogeneous Biodiesel Production

In this work, a cost-effective and environmental catalyst derived from waste clam shell was prepared and investigated in transesterification for biodiesel production. Waste clam shell was treated by acid soaking and then muffles calcinating. The reaction process was conduct in presence of rapeseed oil and methanol using clam shell as catalyst at 65 °C. Using control variable method to investigate the effects of reaction factors including calcination temperature, molar ration of methanol to rapeseed oil, catalyst amounts, reaction time. The result shows that the as-prepared CaO had great performance in the solid base catalytic production of biodiesel. The physical features of the as-prepared CaO derived from clam shell were characterized by using FT-IR, CO2-TPD, XRD, SEM and BET techniques.

Kinetic and Mechanistic Study on Catalytic Decomposition of Hydrogen Peroxide on Carbon-Nanodots/Graphitic Carbon Nitride Composite

The metal-free CDots/g-C3N4 composite, normally used as the photocatalyst in H2 generation and organic degradation, can also be applied as an environmental catalyst by in-situ production of strong oxidant hydroxyl radical (HO·) via catalytic decomposition of hydrogen peroxide (H2O2) without light irradiation. In this work, CDots/g-C3N4 composite was synthesized via an electrochemical method preparing CDots followed by the thermal polymerization of urea. Transmission electron microscopy (TEM), X-Ray diffraction (XRD), Fourier Transform Infrared (FTIR), N2 adsorption/desorption isotherm and pore width distribution were carried out for characterization. The intrinsic catalytic performance, including kinetics and thermodynamic, was studied in terms of catalytic decomposition of H2O2 without light irradiation. The second-order rate constant of the reaction was calculated to be (1.42 ± 0.07) × 10−9 m·s−1 and the activation energy was calculated to be (29.05 ± 0.80) kJ·mol−1. Tris(hydroxymethyl) aminomethane (Tris) was selected to probe the produced HO· during the decomposing of H2O2 as well as to buffer the pH of the solution. The composite was shown to be base-catalyzed and the optimal performance was achieved at pH 8.0. A detailed mechanism involving the adsorb-catalyze double reaction site was proposed. Overall, CDots/g-C3N4 composite can be further applied in advanced oxidation technology in the presence of H2O2 and the instinct dynamics and the mechanism can be referred to further applications in related fields.