Jasmine waste derived biochar as green sulfate catalysts dominate non-free radical paths efficiently degraded tetracycline

生物炭 催化作用 降级(电信) 化学 碳化 电子顺磁共振 激进的 核化学 吸附 化学工程 热解 有机化学 工程类 物理 电信 核磁共振 计算机科学
作者
Xiuchan Xiao,Yaqi Ren,Lei Yan,Xi Li,Hongyang Guo,Chunhong Zhang,Yi Jiao
出处
期刊:Chemosphere [Elsevier]
卷期号:339: 139610-139610 被引量:13
标识
DOI:10.1016/j.chemosphere.2023.139610
摘要

Because of the potential environmental harm caused by the extensive application of tetracycline (TC), this study used jasmine waste rich in organic matter as a precursor and one-step carbonization into metal-free carbon-based materials to efficiently activate peroxymonosulfate (PMS) toward degrading TC. The jasmine waste biochar (JWB) with a heating rate of 10 °C min-1 and a heating temperature of 700 °C was selected as the most suitable material based on its catalytic performance. The effects of catalyst dose, PMS dose, initial pH value, coexisting inorganic anions and TC concentration on the JWB/PMS/TC system were thoroughly optimized. The results showed that the degradation efficiency of TC by JWB/PMS system was 90%. Meanwhile, the combination of electron paramagnetic resonance, masking experiments and X-ray photoelectron spectrometry confirmed that JWB degraded TC mainly through the non-radical radical pathway of 1O2 oxidation and mediated the electron transfer to PMS. In addition, some degradation products were analyzed by LC-MS and possible degradation pathways of the system were proposed. Therefore, this paper proposes a novel method for recycling jasmine waste and providing a low-cost catalyst for the oxidation treatment of refractory organic matter.
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