Dataset Information

Synthesis of Novel Kaolin-Supported g-C3N4/CeO2 Composites with Enhanced Photocatalytic Removal of Ciprofloxacin.

ABSTRACT: Herein, novel ternary kaolin/CeO2/g-C3N4 composite was prepared by sol-gel method followed by hydrothermal treatment. The self-assembled 3D "sandwich" structure consisting of kaolin, CeO2 and g-C3N4 nanosheets, was systematically characterized by appropriate techniques to assess its physicochemical properties. In the prerequisite of visible-light irradiation, the removal efficiency of ciprofloxacin (CIP) over the kaolin/CeO2/g-C3N4 composite was about 90% within 150 min, 2-folds higher than those of pristine CeO2 and g-C3N4. The enhanced photocatalytic activity was attributed to the improved photo-induced charge separation efficiency and the large specific surface area, which was determined by electrochemical measurements and N2 physisorption methods, respectively. The synergistic effect between the kaolin and CeO2/g-C3N4 heterostructure improved the photocatalytic performance of the final solid. The trapping and electron paramagnetic resonance (EPR) experiments demonstrated that the hole (h+) and superoxide radicals (•O2-) played an important role in the photocatalytic process. The photocatalytic mechanism for CIP degradation was also proposed based on experimental results. The obtained results revealed that the kaolin/CeO2/g-C3N4 composite is a promising solid catalyst for environmental remediation.

SUBMITTER: Huang Z

PROVIDER: S-EPMC7503662 | biostudies-literature |

REPOSITORIES: biostudies-literature

ACCESS DATA

Similar Datasets

Project description:A highly porous architecture of graphitic carbon nitride g-C3N4/Cu2O nanocomposite in the form of cubes with a side length of ≈ 1 μm, large pores of 1.5 nm, and a high surface area of 9.12 m2/g was realized by an optimized in situ synthesis protocol. The synthesis protocol involves dispersing a suitable "Cu" precursor into a highly exfoliated g-C3N4 suspension and initiating the reaction for the formation of Cu2O. Systematic optimization of the conditions and compositions resulted in a highly crystalline g-C3N4/Cu2O composite. In the absence of g-C3N4, the Cu2O particles assemble into cubes with a size of around 300 nm and are devoid of pores. Detailed structural and morphological evaluations by powder X-ray diffraction and field emission scanning electron microscopy revealed the presence of highly exfoliated g-C3N4, which is responsible for the formation of the porous architecture in the cube like assembly of the composite. The micrographs clearly reveal the porous structure of the composite that retains the cubic shape of Cu2O, and the energy-dispersive spectroscopy supports the presence of g-C3N4 within the cubic morphology. Among the different g-C3N4/Cu2O compositions, CN/Cu-5 with 10% of g-C3N4, which is also the optimum composition resulting in a porous cubic morphology, shows the best visible light photocatalytic performance. This has been supported by the ultraviolet diffuse reflectance spectroscopy (UV-DRS) studies of the composite which shows a band gap of around 2.05 eV. The improved photocatalytic performance of the composite could be attributed to the highly porous morphology along with the suitable optical band gap in the visible region of the solar spectrum. The optimized composite, CN/Cu-5, demonstrates a visible light degradation of 81% for Methylene Blue (MB) and 85.3% for Rhodamine-B (RhB) in 120 min. The decrease in the catalyst performance even after three repeated cycles is less than 5% for both MB and RhB dyes. The rate constant for MB and RhB degradation is six and eight times higher with CN/Cu-5 when compared with the pure Cu2O catalyst. To validate our claim that the dye degradation is not merely decolorization, liquid chromatography-mass spectroscopy studies were carried out, and the end products of the degraded dyes were identified.

Dataset Information

Synthesis of Novel Kaolin-Supported g-C3N4/CeO2 Composites with Enhanced Photocatalytic Removal of Ciprofloxacin.

Similar Datasets

OmicsDI is part of the ELIXIR infrastructure

Tweets