催化作用
零价铁
反应性(心理学)
化学工程
雷尼替丁
材料科学
纳米尺度
降级(电信)
集聚经济
激进的
纳米技术
无机化学
化学
有机化学
吸附
病理
工程类
胃肠病学
替代医学
电信
医学
计算机科学
作者
Yiyang Ma,Xiaofan Lv,Dongbin Xiong,Xuesong Zhao,Zhenghua Zhang
标识
DOI:10.1016/j.apcatb.2020.119720
摘要
Magnetic nanoscale zero-valent iron (nZVI)@Ti3C2-based MXene nanosheets were synthesized via an in-situ reductive deposition method, and were characterized as a novel Fenton-like catalyst for ranitidine degradation. The vast majority of ranitidine was found to be mineralized after 30 min of reaction time with 91.1 % of removal efficiency and the removal of 63.3 % of total organic carbon (TOC). Results showed that the [email protected]3C2-based MXene nanosheets had a synergistic effect enhancing the catalyst chemical reactivity and stability. In particular, Ti3C2-based MXene was found to restrain the agglomeration of nZVI particles (nZVIPs) and promote electron transfer between magnetic particles with a diameter of approximately 10−40 nm. Ranitidine molecules were decomposed mainly by hydroxyl radicals (∙OH) attack especially the surface-bound ∙OHads. This study provided a completely new insight into the mode of surface inactivation of nZVIPs under different solution pH conditions, establishing that this novel catalyst was suitable for use under a wide pH range.
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