Anatase TiO2with exposed{001}facets has been deepgoingly studied for optimizing its photocatalytic activity.In this study,we synthesized N-doped TiO2 nanocrystals with exposed{001}facets by sol–gel method and solvothermal method,respectively.The physical and chemical properties of as-synthesized samples,such as morphology,crystal phase,surface elements composition,porous structure,specific surface area,and optical response,were characterized in detail.The photocatalytic performances of all samples were evaluated by photocatalytic decoloration of methylene blue under visible-light irradiation(k[420 nm).The results showed that the as-prepared samples present high visible-light photocatalytic performances,which can be ascribed to the excellent crystallization,the enhancement of absorbance in the visible-light region,and the strong adsorption performance,and calcination treatment is helpful to further improve the visible-light photocatalytic performance of N-doped TiO2 nanocrystals with exposed{001}facets.
Biogenic manganese oxides(BioMnOx) were synthesized by the oxidation of Mn(II) with Mnoxidizing bacteria Pseudomonas sp. G7 under different initial pH values and Mn(II) dosages, and were characterized by X-ray diffraction, X-ray photoelectron spectroscopy, and UV-Vis absorption spectroscopy. The crystal structure and Mn oxidation states of BioMnOx depended on the initial pH and Mn(II) dosages of the medium. The superoxide radical(O.-2) was observed in Mn-containing(III/IV) BioMnOxsuspensions by electron spin resonance measurements. BioMnOx(0.4)-7, with mixed valence of Mn(II/III/IV) and the strongest O.-2signals, was prepared in the initial pH 7 and Mn(II) dosage of 0.4 mmol/L condition, and exhibited the highest activity for ciprofloxacin degradation and no Mn(II) release. During the degradation of ciprofloxacin, the oxidation of the Mn(II) formed came from biotic and abiotic reactions in BioMnOx suspensions on the basis of the Mn(II) release and O.-2formation from different BioMnOx. The degradation process of ciprofloxacin was shown to involve the cleavage of the hexatomic ring having a secondary amine and carbon-carbon double bond connected to a carboxyl group, producing several compounds containing amine groups as well as small organic acids.
