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通过木质素的同步热解原位限制磁性氧化铁的石墨生物炭作为一种有效的 HO 激活剂,用于快速降解有机污染物。

Graphitic biochar with in situ confined magnetic iron oxides via synchronous pyrolysis of lignin as an effective HO activator for fast degradation of organic pollutants.

机构信息

School of Chemistry and Chemical Engineering, Guangxi Key Laboratory of Petrochemical Resource Processing and Process Intensification Technology, Guangxi University, 100 Daxuedong Road, Nanning 530004, China.

School of Chemistry and Chemical Engineering, Guangxi Key Laboratory of Petrochemical Resource Processing and Process Intensification Technology, Guangxi University, 100 Daxuedong Road, Nanning 530004, China.

出版信息

Int J Biol Macromol. 2022 Apr 30;205:329-340. doi: 10.1016/j.ijbiomac.2022.02.076. Epub 2022 Feb 17.

DOI:10.1016/j.ijbiomac.2022.02.076
PMID:35183602
Abstract

Magnetic iron oxide confined in carbon capsules/biochar composite (FeOx@g-BC) was created using in-situ synchronous pyrolysis of alkali lignin as a low-cost carbon source. Characterization results indicated the FeOx was confined in carbon nanotubes and carbon capsules, inhibiting growing of nanoparticles and deactivation. The composite catalyst demonstrated significant activity in activating HO for the degradation of persistent organic pollutants in water over a wide pH range. Particularly, tetracycline (TC) could be completely degraded within 25 min, even at a high pH of 6.8, which performed much better than previously reported Fenton-like catalysts. Moreover, the excellent magnetism of FeOx@g-BC aided in its recovery and reuse. The stability of FeOx@g-BC recycling was also measured by continuous cycles of reactions. According to ESR analysis and free radical quenching studies, OH and O were discovered as the dominant active species governing the degradation of TC, and two pathways of TC degradation were proposed. This study developed a novel heterogeneous catalyst for catalytic degradation of persistent organic contaminants in water by the value-added usage of lignin.

摘要

采用原位同步热解碱木质素作为低成本碳源,制备了磁性氧化铁限域在碳胶囊/生物炭复合材料(FeOx@g-BC)。表征结果表明,FeOx 被限域在碳纳米管和碳胶囊中,抑制了纳米颗粒的生长和失活。该复合催化剂在很宽的 pH 范围内对 HO 的活化具有显著的活性,用于水中持久性有机污染物的降解。特别是,四环素(TC)在 25 分钟内可完全降解,即使在高 pH 值 6.8 下,其性能也优于先前报道的类芬顿催化剂。此外,FeOx@g-BC 的优异磁性有助于其回收和再利用。还通过连续的反应循环测量了 FeOx@g-BC 回收的稳定性。根据 ESR 分析和自由基猝灭研究,发现 OH 和 O 是降解 TC 的主要活性物质,并提出了 TC 降解的两种途径。该研究通过木质素的增值利用,开发了一种用于水相催化降解持久性有机污染物的新型多相催化剂。

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