Synthesis and application of magnetic materials-barium ferrite nanomaterial as an effective microwave catalyst for degradation of brilliant green.

In this work, magnetic separably barium ferrite nanomaterial (BaFeO) was synthesized via citrate acid assisted sol-gel combustion method. Subsequently, X-ray diffraction (XRD), scanning electron microscopy-energy dispersion spectroscopy (SEM-EDS), transmission electron microscopy (TEM) and vibrating sample magnetometer (VSM) were applied for its structural, morphological, and electromagnetic characterization. In addition, microwave (MW) absorption and thermal conversion test results indicated the BaFeO had electrothermal rather than magnetothermal conversion capacity. Meanwhile, the synthesized BaFeO showed satisfactory performance in both eliminating and mineralization of a typical triphenylmethane dye, brilliant green (BG), in MW-induced catalytic oxidation (MICO) process without extra oxidant addition. Besides, changes in element valence and content of BaFeO before and after MICO process investigated with XRD, Fourier transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS) showed its relatively stable properties. Furthermore, transition oxygen species involved in MICO process was deduced as lattice oxygen species. Then, the possible degradation pathway of BG was proposed as demethylation, open-loop of triphenylmethane, releasing one ring, formation of the benzene ring and the ultimate mineralization based on the degradation intermediates tentatively identified by gas chromatography mass spectrometry (GC/MS) and liquid chromatography mass spectrometry (LC/MS), respectively. Finally, ecotoxicity analysis by ecological structure activity relationships (ECOSAR) showed that both the acute and chronic toxicity of these intermediates were lower than that of parent BG. These findings are important regarding the development of efficient catalysts in MICO process for degradation of BG analogues in wastewater.

Adsorption behavior and mechanism of 9-Nitroanthracene on typical microplastics in aqueous solutions.

Microplastics and Nitropolycyclic aromatic hydrocarbons (NPAHs) are two types of emerging pollutants that are strong potential threats to aquatic ecosystems and organisms. The adsorption of NPAHs on microplastics may explain the fate and effects of NPAHs in natural environments. In this study, the adsorption behavior of 9-Nitroanthrene (9-NAnt) on polyethylene (PE), polypropylene (PP) and polystyrene (PS) was investigated. Kinetic experiments revealed that 9-NAnt was inclined to be adsorbed onto microplastics, especially PE, which had a large adsorption amount of 734 µg g-1. A linear isothermal model better described the isothermal adsorption process for 9-NAnt, which indicated that a hydrophobic distribution may be the main adsorption mechanism in an aqueous solution. Water environment factors, such as the pH and ionic strength, had negligible effects on the adsorption for PE. In contrast, alkaline and high ionic strength conditions resulted in the inhibition of adsorption of PP and PS. In addition, the particle size of microplastics was negatively correlated with the log Kd of 9-NAnt, and the performance of transient aging treatments on microplastics reduced their affinity for 9-NAnt, due to the addition of oxygen-containing functional groups. Above all, hydrophobic and electrostatic processes were the main adsorption mechanisms between microplastics and 9-NAnt.