Key Laboratory for Environmental Pollution Prediction and Control, Gansu Province, College of Earth and Environmental Sciences, Lanzhou University, Lanzhou 730000, China.
College of Chemistry and Environmental Science, Xinjiang Laboratory of Phase Transitions and Microstructures of Condensed Matter Physics, Yili Normal University, Yining 835000, China.
J Environ Sci (China). 2024 Jul;141:235-248. doi: 10.1016/j.jes.2023.07.019. Epub 2023 Jul 28.
In this study, the cobalt-nickel layered double hydroxides (CoNi LDH) were synthesized with a variety of Co/Ni mass ratio, as CoNi LDHs. In comparison, CoNi LDH presented the best peroxymonosulfate (PMS) activation efficiency for 2,4-dichlorophenol removal. Meanwhile, CoNi LDH@Nickel foam (CoNi LDH@NF) composite membrane was constructed for enhancing the stability of catalytic performance. Herein, CoNi LDH@NF-PMS system exerted high degradation efficiency of 99.22% within 90 min for 2,4-DCP when [PMS] = 0.4 g/L, CoNi LDH@NF = 2 cm × 2 cm (0.2 g/L), reaction temperature = 298 K. For the surface morphology and structure of the catalyst, it was demonstrated that the CoNi LDH@NF composite membrane possessed abundant cavity structure, good specific surface area and sufficient active sites. Importantly, ·OH, SO· and O played the primary role in the CoNi LDH@NF-PMS system for 2,4-DCP decomposition, which revealed the PMS activation mechanism in CoNi LDH@NF-PMS system. Hence, this study eliminated the stability and adaptability of CoNi LDH@NF composite membrane, proposing a new theoretical basis of PMS heterogeneous catalysts selection.
在这项研究中,合成了一系列钴镍层状双氢氧化物(CoNi LDH),其钴镍摩尔比不同。相比之下,CoNi LDH 对 2,4-二氯苯酚的去除具有最佳的过一硫酸盐(PMS)活化效率。同时,构建了 CoNi LDH@泡沫镍(CoNi LDH@NF)复合膜以提高催化性能的稳定性。在此,当 [PMS] = 0.4 g/L、CoNi LDH@NF = 2 cm × 2 cm(0.2 g/L)、反应温度 = 298 K 时,CoNi LDH@NF-PMS 体系在 90 min 内对 2,4-DCP 的降解效率高达 99.22%。从催化剂的表面形貌和结构来看,CoNi LDH@NF 复合膜具有丰富的腔结构、良好的比表面积和充足的活性位点。重要的是,在 CoNi LDH@NF-PMS 体系中,·OH、SO·和 O·对 2,4-DCP 的分解起主要作用,揭示了 PMS 在 CoNi LDH@NF-PMS 体系中的活化机制。因此,本研究消除了 CoNi LDH@NF 复合膜的稳定性和适应性问题,为 PMS 非均相催化剂的选择提出了新的理论依据。