Pu Mengjie, Guan Zeyu, Ma Yongwen, Wan Jinquan, Wang Yan, Brusseau Mark L, Chi Haiyuan
College of Environment and Energy, South China University of Technology, Guangzhou 510006, China.
Department of Soil, Water and Environmental Science, School of Earth and Environmental Sciences, University of Arizona, Tucson, AZ, 85721, USA.
Appl Catal A Gen. 2018 Jan 5;549:82-92. doi: 10.1016/j.apcata.2017.09.021. Epub 2017 Sep 20.
A series of MIL-53(Fe) materials were synthesized using a solvothermal method under different temperature and time conditions and were used as catalysts to activate persulfate and degrade Orange G (OG). Influences of the above conditions on the crystal structure and catalytic behavior were investigated. Degradation of OG under different conditions was evaluated, and the possible activation mechanism was speculated. The results indicate that high synthesis temperature (larger than 170 °C) leads to poor crystallinity and low catalytic activity, while MIL-53(Fe) cannot fully develop at low temperature (100 or 120 °C). The extension of synthesis time from 5 h to 3 d can increase the crystallinity of the samples, but weakened the catalytic activity, which was caused by the reduction of BET surface area and the amount of Fe (II)-coordinative unsaturated sites. Among all the samples, MIL-53(Fe)-A possesses the best crystal structure and catalytic activity. In optimal conditions, OG can be totally decolorized after degradation for 90 min, and a removal rate of 74% for COD was attained after 120 min. The initial solution pH had great influence on OG degradation, with the greatest removal in acidic pH environment. ESR spectra showed that sulfate radical (SO ·), hydroxyl radical (OH·), persulfate radical (SO ·), and superoxide radical (O·) exist in this system under acidic conditions. Furthermore, with the increase of pH, the relative amount of O· increases while that of OH· and SO · decreases, resulting in a reduced oxidizing capacity of the system.
采用溶剂热法在不同温度和时间条件下合成了一系列MIL-53(Fe)材料,并将其用作催化剂来活化过硫酸盐并降解橙黄G(OG)。研究了上述条件对晶体结构和催化行为的影响。评估了不同条件下OG的降解情况,并推测了可能的活化机制。结果表明,较高的合成温度(大于170℃)导致结晶度差和催化活性低,而MIL-53(Fe)在低温(100或120℃)下不能充分生长。合成时间从5小时延长至3天可提高样品的结晶度,但催化活性减弱,这是由BET表面积和Fe(II)配位不饱和位点数量的减少所致。在所有样品中,MIL-53(Fe)-A具有最佳的晶体结构和催化活性。在最佳条件下,OG降解90分钟后可完全脱色,120分钟后COD去除率达到74%。初始溶液pH对OG降解有很大影响,在酸性pH环境中去除效果最佳。电子顺磁共振光谱表明,在酸性条件下该体系中存在硫酸根自由基(SO·)、羟基自由基(OH·)、过硫酸根自由基(SO·)和超氧自由基(O·)。此外,随着pH的升高,O·的相对量增加,而OH·和SO·的相对量减少,导致体系氧化能力降低。