Facile integration of a novel Sm-doped CoFe2O4@ g-CN heterostructure to expedite PMS and H2O2 assisted degradation of pharmaceutical pollutants

纳米复合材料 氧化剂 光催化 催化作用 降级(电信) 化学工程 材料科学 异质结 化学 核化学 纳米技术 有机化学 计算机科学 光电子学 电信 工程类
作者
Sneha Singh,Paramdeep Kaur,Abhivyakti,Vinod Kumar,Kulbhushan Tikoo,Sonal Singhal
出处
期刊:Applied Surface Science [Elsevier BV]
卷期号:580: 152254-152254 被引量:24
标识
DOI:10.1016/j.apsusc.2021.152254
摘要

The persistence of pharmaceutical compounds in the aquatic system has cascading effects on environment and the living world. In order to address the grave concerns regarding pharmaceutical pollution, samarium (Sm) doped cobalt nanoferrite (CS) was merged with a π conjugated carbonaceous material i.e. graphitic carbon nitride (g-CN) to form a series of heterojunction nanocomposites, ([email protected]%g-CN) via ultrasonic assisted method. The structure, morphology, magnetic and optical properties of the fabricated nanocomposites were systematically characterized. The synthesized nanocomposites were highly efficient to activate peroxymonosulfate (PMS) and hydrogen peroxide (H2O2) as oxidizing agents for degradation of model pharmaceutical pollutants i.e. levofloxacin, tetracycline, ciprofloxacin and doxorubicin. As compared to H2O2, PMS as oxidant exhibits astonishing results for removal of pollutants. The degradation of tetracycline by employing [email protected] %g-CN (0.25 g/L) nanocomposite as catalyst and PMS (2.2 mM) as oxidant was observed in less than 3 min. Among all, [email protected] %g-CN nanocomposite exhibits highest catalytic activity ascribed to synergistic effect of tunable band structure, high surface area and improved separation of charge carriers across the heterojunction. The newly designed nanocomposites can be recycled up to four catalytic cycles and thus offers a promising strategy in meeting future environmental claims for the removal of refractory compounds from wastewater.

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