Guangdong Key Laboratory of Environmental Catalysis and Health Risk Control, Guangzhou Key Laboratory Environmental Catalysis and Pollution Control, Institute of Environmental Health and Pollution Control, School of Environmental Science and Engineering, Guangdong University of Technology, Guangzhou, 51006, People's Republic of China.
School of Chemical Engineering, University of Adelaide, Adelaide, SA, 5005, Australia.
Water Res. 2019 Dec 1;166:115043. doi: 10.1016/j.watres.2019.115043. Epub 2019 Sep 4.
Multi-walled carbon nanotubes (MWCNTs)/peroxydisulfate (PDS) is a green oxidative system for abatement of aqueous organic pollutants, while the powder form and poor cycling performance of the catalyst limit its practical application. To solve these problems, fabricating a MWCNT cathode (negative polarization) to coupling carbocatalysis-driven PDS activation with electrosorption of organic pollutant was previously demonstrated to be a possible solution to these problems. To further improve the activation efficiency of PDS, positive polarization of MWCNT electrode (anode) was adapted to activate PDS for removing acyclovir and phenol in this work. Under a working voltage of 1.2 V, the MWCNT anode was more efficient than the MWCNT cathode and the non-polarized MWCNT electrode for PDS activation and removal of organic pollutants, owing to the enhanced attraction between SO anions and anode. Although the positive/negative polarization of MWCNT electrode doesn't alter the nonradical mechanism involved in MWCNTs/PDS system, theoretical calculations suggest that different polarization affect the electron configuration and oxidative capacity of activated SO bounded to MWCNTs differently, and that the adsorbed SO with stretched S-O bond and much higher oxidative capacity than that in the case of non-polarized MWCNT electrode is responsible for the MWCNTs anode, while adsorbed SO with stretched O-O bond and slightly higher oxidative capacity is responsible for the MWCNTs cathode. Finally, implications of operation parameters including electrode potential, energy cost, pH, etc. on the elimination efficiency by MWCNT anode/PDS system were investigated and the results suggest that the MWCNT anode/PDS is an efficient and economical metal-free electrochemical oxidative system for organic contaminants remediation.
多壁碳纳米管 (MWCNTs)/过一硫酸盐 (PDS) 是一种用于去除水中有机污染物的绿色氧化体系,然而催化剂的粉末形式和较差的循环性能限制了其实际应用。为了解决这些问题,以前曾证明构建 MWCNT 阴极(负极)以偶联碳催化驱动的 PDS 活化与有机污染物的电吸附是解决这些问题的一种可能方法。为了进一步提高 PDS 的活化效率,本工作采用 MWCNT 电极(阳极)的正极化来活化 PDS 以去除阿昔洛韦和苯酚。在 1.2 V 的工作电压下,MWCNT 阳极比 MWCNT 阴极和非极化 MWCNT 电极更有效地活化 PDS 和去除有机污染物,这归因于 SO42-阴离子与阳极之间的增强吸引力。尽管 MWCNT 电极的正/负极化不会改变 MWCNTs/PDS 体系中涉及的非自由基机制,但理论计算表明,不同的极化会以不同的方式影响与 MWCNTs 结合的活化 SO 的电子构型和氧化能力,并且具有拉伸 S-O 键和比非极化 MWCNT 电极情况下更高氧化能力的吸附 SO 负责 MWCNTs 阳极,而具有拉伸 O-O 键和略高氧化能力的吸附 SO 负责 MWCNTs 阴极。最后,研究了包括电极电位、能源成本、pH 值等操作参数对 MWCNT 阳极/PDS 系统去除效率的影响,结果表明,MWCNT 阳极/PDS 是一种高效且经济的无金属电化学氧化体系,可用于修复有机污染物。