Microwave-Assisted Solvothermal Synthesis of Fe3O4/CeO2 Nanocomposites and Their Catalytic Activity in the Imine Formation from Benzyl Alcohol and Aniline

Fe3O4/CeO2 nanocomposites were synthetized by coating magnetite seeds of different morphologies (hexagonal, spheroidal, quasi-spherical) with ceria, in ethylene glycol as solvothermal solvent. The synthesis was performed in the presence of microwave irradiation aiming to overcome the common disadvantages proper of the classic solvothermal/hydrothermal procedure. The obtained nanocomposites were calcined at the optimum temperature of 550 °C. The structure of the new nanomaterials was carefully investigated by IR, XRD, SEM, EDS and TEM analyses. The nanocomposites resulted to be constituted by CeO2 nanoparticles distributed onto Fe3O4 seeds, that kept their pristine morphology. The new materials were used as catalysts for imine synthesis from benzyl alcohol and aniline. The highest imine conversion rate was obtained with Fe3O4/CeO2, which was synthesized from Fe3O4 nanoparticles (hexagonal) obtained by microwave hydrothermal procedure in the absence of any organic additive (polyvinylpyrrolidone, trisodium citrate dihydrate or oleic acid). The catalyst could be easily removed from the reaction mixture with the help of an external magnet, and it was recycled for at least five runs with increasing catalytic activity.

Synthesis of ZnO Hollow Microspheres and Analysis of Their Gas Sensing Properties for n-Butanol

ZnO hollow microspheres with a diameter of approximately 1.4 μm were successfully synthesized by a facile one-step chemical precipitation method using trisodium citrate dihydrate as a morphology control agent. The ZnO hollow microspheres consisted of nanoplates and had good dispersibility. Control experiments revealed that trisodium citrate dihydrate played an important role in regulating the morphologies of ZnO products. The morphology of the ZnO product evolved from nanowires to hollow microspheres with the addition of trisodium citrate dihydrate. The sensor response of ZnO hollow microspheres toward 100 ppm n-butanol reached 86.6 at the optimum operating temperature of 340 °C, which was approximately three times higher than that of ZnO nanowires. In addition, the ZnO hollow microspheres also displayed good selectivity and long-term work stability toward n-butanol. The excellent gas sensing performance of ZnO hollow microspheres may be ascribed to the unique hollow sphere structure with high exposed polar crystal surface.

One-step preparation of carbon dot-grafted trisodium citrate dihydrate for tunable photoluminescence and white light-emitting diodes

Emitting-color of (B-CDs/SC and Y-CDs/SC)-based composites can be systematically tailored. Meanwhile, both of them can be successfully fabricated in WLEDs.

Rapid Determination of Nitroimidazole Residues in Honey by Liquid Chromatography/Tandem Mass Spectrometry

We developed a rapid and efficient means of determining residues of four nitroimidazoles—i.e., dimetridazole, ipronidazole, metronidazole, and ronidazole—and three hydrophilic metabolites—i.e., 2-hydroxymethyl-1-methyl-5-nitroimidazole, 1-methyl-2-(2′-hydroxyisopropyl)-5-nitroimidazole, and 1-(2-hydroxyethyl)-2-hydroxymethyl-nitroimidazole—in honey. We applied a QuEChERS (Quick, Easy, Cheap, Effective, Rugged, and Safe) procedure improved to suit a nitroimidazole analysis, which is fast (approximately 30 min) and uses less organic solvent. The procedure involves initial single-phase extraction of 5 g of honey with acetonitrile containing 1% acetic acid, followed by liquid–liquid partitioning involving the addition of 5 g sodium chloride, 1.5 g trisodium citrate dihydrate, and 4 g magnesium sulfate. Moreover, matrix from honey was reduced by an SPE method with an alumina-N cartridge. The samples were analyzed using LC/MS/MS. Chromatographic separation of these nitroimidazoles and metabolites was performed in the gradient mode on a pentafluorophenylpropyl-bonded silica column (150 × 2.0 mm, 3 μm particle size) at 40°C. The mobile phase consisted of a 0.01% acetic acid solution and acetonitrile, and the flow rate was 0.2 mL/min. The method was validated using honey spiked with these nitroimidazoles from 0.1 to 0.5 μg/kg. The overall recovery of the seven nitroimidazoles ranged from 76.1 to 98.5%; intra- and interassay CV values were <9.5 and <14.2%, respectively. The LOQ ranged from 0.1 to 0.5 μg/kg. LC/MS/MS coupled with the QuEChERS method showed good potential as a method for determining nitroimidazole residues in honey.