Fabrication of nanostructured NiO/WO3 with graphitic carbon nitride for visible light driven photocatalytic hydroxylation of benzene and metronidazole degradation

被引:31
作者
Devi, Meghaii [1 ]
Das, Bishal [1 ]
Barbhuiya, Monjur Hassan [1 ]
Bhuyan, Bishal [1 ]
Dhar, Siddhartha Sankar [1 ]
Vadivel, Sethumathavan [2 ]
机构
[1] Natl Inst Technol, Dept Chem, Cachar 788010, Assam, India
[2] PSG Coll Technol, Dept Chem, Coimbatore 641004, Tamil Nadu, India
关键词
IN-SITU SYNTHESIS; CATALYTIC HYDROXYLATION; SELECTIVE HYDROXYLATION; HYDROGEN-PEROXIDE; FACILE SYNTHESIS; H-2; GENERATION; PHENOL; OXIDATION; OXIDE; TIO2;
D O I
10.1039/c9nj02904d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In the present study, we report a novel nanocatalyst prepared by the modification of g-C3N4 nanosheets with a NiO/WO3 nanohybrid via a simple ultra-sonication method. A novel method was employed for the synthesis of the NiO/WO3 nanohybrid. The photocatalytic efficiency of the catalysts was explored in C-H activation and degradation of a product commonly found in pharmaceutical waste, namely metronidazole. The photocatalyst recorded a rapid and highly selective conversion of benzene to phenol under irradiation using a LED bulb. Degradation of metronidazole was carried out both in the presence of sunlight and LED light and monitored using UV-vis spectroscopy. It was observed that the degradation process was more efficient under solar light irradiation, where complete degradation was recorded in 90 minutes with a rate constant of 0.0165 min(-1). The modified photocatalyst showed much higher efficiency when compared to the individual components of g-C3N4 and nanostructured NiO/WO3. The structural features of the photocatalyst were thoroughly investigated using powder XRD, SEM, TEM, XPS, UV-DRS, PL and BET analysis. This enhanced efficiency is attributed to a larger surface area, lower band gap and delayed recombination of photogenerated charge carriers at the heterojunction. The critical involvement of photoactive radicals in the degradation process was thoroughly investigated by trapping experiments using photoluminescence spectroscopy.
引用
收藏
页码:14616 / 14624
页数:9
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