کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5353662 1503580 2016 8 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Fabrication of highly active Melem/Zn0.25Cd0.75S composites for the degradation of bisphenol A and methyl orange under visible light irradiation
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی تئوریک و عملی
پیش نمایش صفحه اول مقاله
Fabrication of highly active Melem/Zn0.25Cd0.75S composites for the degradation of bisphenol A and methyl orange under visible light irradiation
چکیده انگلیسی
Metal-free polymeric catalyst hold great promise owing to their abundant sources, low-cost fabrication and easy processibility. Melem, an important intermediate during condensation of melamine rings to graphitic carbon nitride (g-C3N4), was synthesized by simple solid phase polymerization process. A novel Melem/Zn0.25Cd0.75S composite was fabricated through a facile one-step hydrothermal method. The as-products were characterized by X-ray diffraction (XRD), UV-vis DRS spectroscopy, fourier transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), high resolution transmission electron microscopy (HRTEM). The TEM and HRTEM results reveal that Zn0.25Cd0.75S nanoparticles and Melem closely contact with each other to form an intimate interface. The as-prepared composites exhibit significantly enhanced visible light photocatalytic performance for the degradation of Methyl orange (MO) and Bisphenol A (BPA), which could be attributed to the effective photo-induced charges transfer and separation in Melem/Zn0.25Cd0.75S composites. On the basis of radical scavenger experiments, superoxide radicals and holes are suggested to play a critical role in MO degradation over Melem/Zn0.25Cd0.75S heterojunctions. A possible mechanism for charge separation and transfer in the Melem/Zn0.25Cd0.75S composites was proposed to explain the enhanced photocatalytic performance.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Applied Surface Science - Volume 387, 30 November 2016, Pages 513-520
نویسندگان
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