Zhang Guoliang, Qin Lei, Wu Yujiao, Xu Zehai, Guo Xinwen
Institute of Oceanic and Environmental Chemical Engineering, College of Chemical Engineering and Material Science, Zhejiang University of Technology, Hangzhou 310014, China.
Nanoscale. 2015 Jan 21;7(3):1102-9. doi: 10.1039/c4nr05884d.
A novel SiO2 nanosphere was synthesized by the post-synthetic grafting of sulfonic acid groups on to anionic-surfactant-templated mesoporous NH2-silica (AMAS). This one-pot post-functionalization strategy allowed more metal ions to be homogeneously anchored into the channel of the meso-SiO2 nanosphere. After hydrothermal and calcination treatment, the in situ growth of α-Fe2O3 on sulfonic acid-functionalized mesoporous NH2-SiO2 (SA-AMAS) exhibited much higher activity in the visible-light assisted Fenton reaction at neutral pH than that for AMAS or meso-SiO2 nanospheres. By analysis, the grafted sulfonic acid group can not only enhance the acid strength of the catalyst, but can also bring more orbital-overlapping between the active sites (Fe(II) and Fe(III)) and the surface peroxide species, to facilitate the decomposition of H2O2 to hydroxyl radical. The present results provide opportunities for developing heterogeneous catalysts with high-performance in the field of green chemistry and environmental remediation.
通过将磺酸基团后合成接枝到阴离子表面活性剂模板化的介孔NH2 - 二氧化硅(AMAS)上,合成了一种新型SiO2纳米球。这种一锅法后功能化策略使更多金属离子能够均匀地锚定在介孔SiO2纳米球的通道中。经过水热和煅烧处理后,磺酸功能化介孔NH2 - 二氧化硅(SA - AMAS)上原位生长的α - Fe2O3在中性pH值的可见光辅助芬顿反应中表现出比AMAS或介孔SiO2纳米球更高的活性。通过分析,接枝的磺酸基团不仅可以增强催化剂的酸强度,还可以使活性位点(Fe(II)和Fe(III))与表面过氧化物物种之间产生更多的轨道重叠,以促进H2O2分解为羟基自由基。目前的结果为在绿色化学和环境修复领域开发高性能的多相催化剂提供了机会。