双酚A
催化作用
X射线光电子能谱
介孔材料
吸附
扫描电子显微镜
多孔性
降级(电信)
化学工程
化学
分解
臭氧
透射电子显微镜
比表面积
材料科学
核化学
有机化学
环氧树脂
复合材料
计算机科学
工程类
电信
作者
Xiuqin Tan,Yifeng Wan,Yajing Huang,Chun He,Zaili Zhang,Zhuoyan He,Lingling Hu,Jiawei Zeng,Dong Shu
标识
DOI:10.1016/j.jhazmat.2016.09.013
摘要
Three-dimensional (3D) MnO2 porous hollow microspheres (δ- and α- MnO2 PHMSs), with high adsorption and catalytic ozonation performance, were synthesized by a self-template (MnCO3 microspheres) process at room temperature. The synthesized MnO2 PHMSs were characterized by X-ray diffraction (XRD), scanning electronic microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS) and Brunauer-Emmett-Teller (BET) surface area. The results showed that PHMSs exhibit the excellent adsorption ability and catalytic activity owning to their hollow spherical structure, mesoporous shell and well-defined interior voids, leading to the strong adsorption for bisphenol A (BPA) and the retention of O3 molecules on catalyst. Moreover, the catalytic performance of α-MnO2 PHMSs was better than that of δ-MnO2 PHMSs which was attributed to the richer lattice oxygen of α-MnO2 PHMSs to accelerate O3 decomposition by producing more reactive oxidative species. The degradation efficiency of BPA using 3D α-MnO2 PHMSs was more than 90% in the presence of ozone within 30min reaction time. The probe tests for reactive oxidative species (ROSs) displayed that BPA degradation by catalytic ozonation is dominated by O2- and OH in our present study. Furthermore, the organic compounds as intermediates of the degradation process were identified by LC/MS.
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