刚果红
亚甲蓝
X射线光电子能谱
光催化
复合数
咪唑酯
化学工程
光降解
打赌理论
漫反射红外傅里叶变换
傅里叶变换红外光谱
纳米颗粒
核化学
比表面积
金属有机骨架
化学
催化作用
材料科学
纳米技术
无机化学
吸附
有机化学
复合材料
工程类
作者
Ramesh Chandra,Mala Nath
标识
DOI:10.1016/j.jwpe.2020.101266
摘要
Abstract Photocatalytic degradation of organic dyes using novel metal based composite materials is one of the most intriguing and sustainable ways to reduce water pollution. Herein, facile synthesis of AgNPs@ZIF-8 via in situ generation of AgNPs and ZIF-8 (Zeolitic Imidazolate Framework) was demonstrated, and composites with different Ag contents (abbreviated as SZ, SZ1, SZ2 SZ3) were well characterized by powder X-ray diffraction (PXRD) pattern, X-ray photoelectron spectroscopy (XPS) and Fourier transform infra-red (FT-IR) spectroscopy. Encapsulation/decoration of AgNPs (particle size: 96 nm in SZ and 17.32 ± 2.35 nm in SZ1 to SZ3) in ZIF-8 matrix has been ensured by TEM and EDX analysis. Brunauer-Emmett-Teller (BET) adsorption-desorption studies indicate that the surface area of SZ (982 m2 g−1) is less than those of SZ1 to SZ3 (due to the encapsulation of large amount of Ag nanoparticles in SZ). The synthesized composites are thermally stable up to 400 °C in air and nitrogen atmosphere. AgNPs@ZIF-8 exhibited excellent photocatalytic efficiency to degrade organic dyes compared to ZIF-8 due to its large surface area, highly porous and unique synergistic properties. SZ2 degrades off 97.25 % methylene blue (MB) and 100 % congo red (CR) at pH ≥ 7. Further, degraded fragments were analysed by GC–MS and plausible degradation mechanism was discussed.
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