降级(电信)
原位
化学
卡马西平
化学工程
材料科学
有机化学
癫痫
计算机科学
电信
生物
工程类
神经科学
作者
Jiali Zhang,Jian Wei,Zhuang Guo,Qingyue Luo,Junfeng Dou,Yonghui Song
标识
DOI:10.1016/j.jclepro.2024.141546
摘要
Abundant exposed ligand-unsaturated sites of Co have been found to enhance the catalytic oxidation property of ZIF-67 material for peroxymonosulfate (PMS) catalysis. Nevertheless, serious stacking of ZIF-67 still poses a challenge to its application. Herein, we employed a specific in situ growth strategy to establish an LDHNS@ZIF-67 composite based on morphology modulation and performance optimization for carbamazepine (CBZ) degradation. ZIF-67 crystals were successfully grown in situ via nucleating on the CoAl-LDH nanosheets (LDHNSs) substrate surface, which facilitated the crystals' dispersion. LDHNS@ZIF-67 (0.1 M) was optimized to display outstanding PMS catalytic activity for CBZ degradation, with almost 100% degradation in 5 min (PMS dose, 0.2 mM, catalyst dose, 25 mg/L, and CBZ concentration, 5 ppm). Quenching and electron paramagnetic resonance (EPR) tests confirmed that both radical substances (SO4•-) and nonradical substances (1O2) dominated the reaction system. As the active site, Co(II) ions on the LDHNS@ZIF-67 (0.1 M) surface effectively promoted active substance formation. The intermediate degradation products and pathways for CBZ were investigated. Toxicity assessment for CBZ and its intermediates was conducted. This work will broaden the application of ZIF-67 materials in advanced oxidation process design based on persulfate.
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