Over the past few years, pharmaceutical drugs have been considered as emerging pollutants due to their continuous input and persistence in the aquatic ecosystem even at low concentrations. They have been detected worldwide in environmental matrices, indicating their ineffective removal from water and wastewaters using conventional methods. In this study we present photocatalytic purification of water from Acetaminophen and Chloramphenicol by ZnO upon UV-light illumination. Commercial ZnO powders are activated thermally (annealed at different temperatures-100, 200, 300, 400 and 500 °C for 1 h) and mechanically (treated for 5, 15, 20, 30, 40 and 60 min). The mechonoactivation is performed varying the atmosphere in air, or in suspension of ethanol and methanol. The changes in the studied material (phase composition, structure and particle size of the samples) and morphology have been investigated by means of X-ray diffraction and Scanning electron microscopy. The ZnO powders annealed at 100 °C show highest photocatalytic efficiency and rate constant of dye degradation, which is due to the smaller size of nanocrystallites and their better developed surface. The degradation rate of Acetaminophen and Chloramphenicol increases with time of mechanical activation up to 30 min and then decreases. The optimal temperature and time of mechanoactivation are experimentally established.
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http://dx.doi.org/10.1007/s12272-016-0789-6 | DOI Listing |
Angew Chem Int Ed Engl
December 2024
University of Science and Technology of China, Hefei National Research Center for Physical Sciences at Microscale, jinzhai road, hefei, CHINA.
Herein, we first report a photocatalytic OCM using CO2 as a soft oxidant for C2H6 production under mild conditions, where an efficient photocatalyst with unique interface sites is constructed to facilitate CO2 adsorption and activation, while concurrently boosting CH4 dissociation. As a prototype, the Au quantum dots anchored on oxygen-deficient TiO2 nanosheets are fabricated, where the Au-Vo-Ti interface sites for CO2 adsorption and activation are collectively disclosed by in situ Kelvin probe force microscopy, quasi in situ X-ray photoelectron spectroscopy and theoretical calculations. Compared with single metal site, the Au-Vo-Ti interface sites exhibit the lower CO2 adsorption energy and decrease the energy barrier of the *CO2 hydrogenation step from 1.
View Article and Find Full Text PDFMacromol Rapid Commun
December 2024
Key Laboratory of Synthetic and Biological Colloids, Ministry of Education, School of Chemical and Material Engineering, Jiangnan University, Wuxi, 214122, China.
Diatomic catalysts enhance photocatalytic CO reduction through synergistic effects. However, precisely regulating the distance between two catalytic centers to achieve synergistic catalysis poses significant challenges. In this study, a series of one-dimensional (1D) covalent organic frameworks (COFs) are designed with adjustable micropores to facilitate efficient CO photoreduction.
View Article and Find Full Text PDFSci Rep
December 2024
School of Physics and Materials Science, Shoolini University, Solan, H.P., India.
The industrial sector faces a significant challenge in finding the highly effective and efficient treatments for harmful dye-based color effluents. In this study, pure and cobalt doped barium hexaferrite of chemical formula, BaCoFeO (x = 0-0.06) are made via sol-gel auto-combustion (SC) methodology.
View Article and Find Full Text PDFSci Rep
December 2024
Department of Physics, Faculty of Science, Islamic University of Madinah, Madinah 42351, Saudi Arabia.
Modifying ZnO nanorods with graphene oxide (GO) is crucial for enhancing photocatalytic degradation by boosting the concentration of reactive oxygen species (ROS) in the reaction medium. In this study, we present a straightforward chemical synthesis of ZnO nanorods embedded on GO, forming a novel nanocomposite, GOZ. This composite serves as an efficient photocatalyst for the sunlight-driven degradation of methylene blue (MB) and ciprofloxacin (CIP).
View Article and Find Full Text PDFJ Colloid Interface Sci
December 2024
Key Laboratory of Functional Inorganic Material Chemistry, Ministry of Education of the People's Republic of China, Heilongjiang University, Harbin 150080, PR China. Electronic address:
Photocatalytically reducing CO into high-value-added chemical materials has surfaced as a viable strategy for harnessing solar energy and mitigating the greenhouse effect. But the inadequate separation of the photogenerated electron-hole pair remains a major obstacle to CO photoreduction. Constructing heterostructure photocatalysts with efficient interface charge transfer is a promising approach to solving the above problems.
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