Asif Muhammad Bilal, Kang Hongyu, Zhang Zhenghua
Institute of Environmental Engineering & Nano-Technology, Tsinghua-Shenzhen International Graduate School, Tsinghua University, Shenzhen 518055, Guangdong, China; Guangdong Provincial Engineering Research Center for Urban Water Recycling and Environmental Safety, Tsinghua-Shenzhen International Graduate School, Tsinghua University, Shenzhen 518055, Guangdong, China; School of Environment, Tsinghua University, Beijing 100084, China.
Institute of Environmental Engineering & Nano-Technology, Tsinghua-Shenzhen International Graduate School, Tsinghua University, Shenzhen 518055, Guangdong, China; Guangdong Provincial Engineering Research Center for Urban Water Recycling and Environmental Safety, Tsinghua-Shenzhen International Graduate School, Tsinghua University, Shenzhen 518055, Guangdong, China; School of Environment, Tsinghua University, Beijing 100084, China.
J Hazard Mater. 2022 Mar 5;425:127988. doi: 10.1016/j.jhazmat.2021.127988. Epub 2021 Dec 3.
For the first time in this study, CoAl-layered double hydroxide nanosheet membrane (LDH) with abundant active sites was fabricated for peroxymonosulfate (PMS) activation with the mindset to catalytically degrade micropollutants. Depending on the catalyst loading, the developed LDH can be driven under gravity at a permeate flux of approximately 80 L/m h and 210 L/m h at LDH loading of 0.80 mg/cm and 0.08 mg/cm, respectively. Notably, the LDH (0.63 mg) exhibited excellent PMS activation efficiency as indicated by 87.8% removal of the probe chemical (ranitidine) at 0.2 mM PMS, which was higher than that (37-44%) achieved by conventional LDH (5-20 mg)/PMS (0.2 mM) system. In addition to efficient degradation of several micropollutants, LDH/PMS performance was not inhibited by variation in solution pH (4-8) as well as during long-term (29 h) continuous-flow operation. SO and O were identified as the primary reactive species in the LDH/PMS system, while both Co and Al participated in PMS activation. This study offers a simple strategy for efficient removal of several micropollutants with significantly reduced catalyst leaching, which could be applied sustainably in water treatment.
在本研究中,首次制备了具有丰富活性位点的钴铝层状双氢氧化物纳米片膜(LDH),用于活化过一硫酸盐(PMS)以催化降解微污染物。根据催化剂负载量,所制备的LDH在重力驱动下,当LDH负载量分别为0.80 mg/cm²和0.08 mg/cm²时,渗透通量约为80 L/m²·h和210 L/m²·h。值得注意的是,LDH(0.63 mg)表现出优异的PMS活化效率,在0.2 mM PMS条件下,探针化学品(雷尼替丁)的去除率达到87.8%,高于传统LDH(5 - 20 mg)/PMS(0.2 mM)体系所达到的去除率(37 - 44%)。除了能有效降解多种微污染物外,LDH/PMS体系的性能不受溶液pH值变化(4 - 8)以及长期(29 h)连续流运行的影响。SO和O被确定为LDH/PMS体系中的主要活性物种,而Co和Al均参与了PMS的活化。本研究提供了一种简单的策略,可有效去除多种微污染物,同时显著减少催化剂浸出,有望在水处理中可持续应用。