通过在榴莲皮生物炭中共同掺入 N 和 S,将过一硫酸盐活化转化为单线态氧主导的氧氟沙星降解途径

IF 13.3 1区 工程技术 Q1 ENGINEERING, CHEMICAL Chemical Engineering Journal Pub Date : 2024-02-03 DOI:10.1016/j.cej.2024.149099
Nguyen Trung Dung , Vu Dinh Thao , Nguyen Phuong Thao , Cao Thi Minh Thuy , Nguyen Hong Nam , Le Viet Ngan , Kun-Yi Andrew Lin , Ta Cong Khiem , Nguyen Nhat Huy
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引用次数: 0

摘要

生物炭是一种环境友好型材料,在水处理方面有多种潜在应用。本文以农业废弃物榴莲皮为原料,通过热处理与硫脲偶联,制备了氮硫共掺杂生物炭(N,S-BCD-X),以激活过一硫酸盐(PMS)来降解水中的氧氟沙星(OFX)。经 N,S-BCD-800 活化的 PMS 在反应 120 分钟后对 OFX 的去除率超过 85%,是纯 BCD 去除率的 17.78 倍。在 3 到 9 的广泛 pH 值范围内,OFX 降解均未受到抑制。通过自由基淬灭试验、电子顺磁共振和 DFT 计算,N,S-BCD-800/PMS 体系中的关键反应物是 1O2,因为 PMS 的 O-O 键拉长会促进 -OH 和 SO4 的生成,但其贡献微乎其微,而 1O2 则是通过与 -OH、SO4 和 PMS 相关的各种反应生成的。N,S-BCD-800 催化活性的提高主要来自于 N 和 S 共掺杂的协同效应,这是因为功函数的降低增强了电子负载能力。此外,静电势的增加以及电子密度和原子电荷的差异也可能是 PMS 在 N,S-BCD-800 上吸附和活化更强的原因,从而产生更多的 1O2,而 N,S-BCD-800/PMS 复合物则是通过电子传递降解 OFX 的次要物种。最后,N,S-BCD/PMS 在各种水基质中以及经过 5 个循环后实现了对 OFX 的高效降解,这证明 N,S-BCD 具有很高的稳定性和适用性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Turning peroxymonosulfate activation into singlet oxygen-dominated pathway for ofloxacin degradation by co-doping N and S into durian peel-derived biochar

Biochar is an environmentally friendly material with various potential applications in water treatment. Herein, nitrogen and sulfur co-doped biochars (N,S-BCD-X) were fabricated from durian peel as an agricultural waste by coupling with thiourea via thermal treatment to activate peroxymonosulfate (PMS) for degradation of ofloxacin (OFX) in water. The OFX removal using PMS activated by N,S-BCD-800 was over 85 % after 120 min of reaction, which was 17.78 times higher than that by pure BCD. The OFX degradation was not inhibited over a wide pH range of 3 to 9. Through radical quenching tests, electron paramagnetic resonance, and DFT calculations, 1O2 was revealed as the key reactive species in the N,S-BCD-800/PMS system because of PMS’s elongated O-O bond-induced promoted generation of OH and SO4- with an insignificant contribution and the generation of 1O2 via various reactions associated with OH, SO4-, and PMS. The boosted catalytic activity of N,S-BCD-800 mainly came from synergetic effect of N and S co-doping due to the enhanced electron-donating capability caused by decrease in the work function. Furthermore, the increase in electrostatic potential and the difference in electron density and atomic charge could also account for stronger adsorption and activation of PMS on N,S-BCD-800 to generate more 1O2 besides the N,S-BCD-800/PMS complex as a minor species responsible for the degradation of OFX via electron transfer. Finally, the attainment of high efficiency of N,S-BCD/PMS for OFX degradation in various water matrices as well as after 5 cycles proved that N,S-BCD had high stability and applicability.

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来源期刊
Chemical Engineering Journal
Chemical Engineering Journal 工程技术-工程:化工
CiteScore
21.70
自引率
9.30%
发文量
6781
审稿时长
2.4 months
期刊介绍: The Chemical Engineering Journal is an international research journal that invites contributions of original and novel fundamental research. It aims to provide an international platform for presenting original fundamental research, interpretative reviews, and discussions on new developments in chemical engineering. The journal welcomes papers that describe novel theory and its practical application, as well as those that demonstrate the transfer of techniques from other disciplines. It also welcomes reports on carefully conducted experimental work that is soundly interpreted. The main focus of the journal is on original and rigorous research results that have broad significance. The Catalysis section within the Chemical Engineering Journal focuses specifically on Experimental and Theoretical studies in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. These studies have industrial impact on various sectors such as chemicals, energy, materials, foods, healthcare, and environmental protection.
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