Polydopamine-modified MOF-5-derived carbon as persulfate activator for aniline aerofloat degradation

化学 过硫酸盐 苯胺 过硫酸钠 降级(电信) 激进的 热解 碳纤维 化学工程 无机化学 核化学 有机化学 材料科学 催化作用 工程类 复合材料 复合数 电信 计算机科学
作者
Congcong Feng,Shaobo Liu,Xiaofei Tan,Mingchong Dai,Qiang Chen,Xinyi Huang
出处
期刊:Chemosphere [Elsevier]
卷期号:345: 140436-140436 被引量:1
标识
DOI:10.1016/j.chemosphere.2023.140436
摘要

Residual flotation chemicals in beneficiation wastewater seriously threaten local ecosystems, such as groundwater or soil, and must be treated effectively. Currently, the degradation of organic pollutants using nitrided MOFs-derived carbon to activate persulfate (PDS) has attracted considerable attention. Hence, we developed a new synthetic strategy to load dopamine hydrochloride (PDA) onto MOF-5-derived porous carbon (PC) to form NPC, and the degradation of a typical flotation Aniline aerofloat (AAF) at high salinity by a low dose of the NPC/PDS system was investigated. Several characterization analyses such as TEM, XRD, Raman, FT-IR and XPS demonstrated that the nitrogen-rich indolequinone unit in PDA provided nitrogen to PC during the pyrolysis process. This enabled the core-shell structure of NPC and the synergy among the multiple components to induce the AAF degradation by PDS over a wide pH scale in a short period of time. It was deduced that the degradation of AAF by the NPC-8/PDS system was a non-radical pathway dominated by 1O2, which relied mainly on the conversion of superoxide radicals (O2•−) and surface-bound radicals. Among them, the pyridine N in the sp2 hybrid carbon was considered as a possible active site. This non-radical pathway was resistant to pH changes and background substances in the water, and well overcame the inhibition of the reaction by natural organic substances and inorganic anions in natural water. In this study, A novel approach to the synthesis of homogeneous MOFs nuclear-derived porous carbon was proposed and the application of MOFs-derived porous carbon for AAF remediation of mineral processing wastewater was broadened.
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