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基于杂化绿色 DNSA@壳聚糖@MnFeO 可见光激活的芬顿样纳米催化剂用于亚甲基蓝的光降解。

Fenton-like nanocatalyst for photodegradation of methylene blue under visible light activated by hybrid green DNSA@Chitosan@MnFeO.

机构信息

Institute of Nanoscience & Nanotechnology, Kafrelsheikh University, 33516 Kafrelsheikh, Egypt.

Faculty of Science, Kafrelsheikh University, 33516 Kafrelsheikh, Egypt.

出版信息

Carbohydr Polym. 2018 Oct 1;197:17-28. doi: 10.1016/j.carbpol.2018.05.076. Epub 2018 May 26.

DOI:10.1016/j.carbpol.2018.05.076
PMID:30007602
Abstract

High efficient 3,5-Dinitrosalicylic acid/Chitosan/MnFeO (DNSA@CS@MnFeO) nano photocatalyst was prepared to enrich both adsorption and photodecomposition under visible light. This paper focused on the importance of DNSA@CS as an excellent connector between methylene blue (MB) and MnFeO for accelerating photodegradation with the encouragement of photo-Fenton catalytic reagent hydrogen peroxide (HO). The optimum conditions were: contact time, 30 min, HO concentration, 0.16 M, pH factor 9 and dosage 0.06 g/l at R.T, allowing excellent catalytic achievements 98.9% degree of decolorization in 30 min. More interestingly, the hybrid DNSA@CS@MnFeO mechanism explained on the basis of coexistence of Mn/Mn and Fe/Fe redox couples during the reaction. The photocatalytic decolorization experimentally affirmed the suitability of DNSA@CS@MnFeO obeying Langmuir-Hinshelwood model. Also, the nano-catalytic system was stable even after five runs. The prepared nanostructured catalyst provides simple fabrication to promote deep understand criteria for the mechanistic role of MnFeO catalyst for degradation of MB molecules.

摘要

高效的 3,5-二硝基水杨酸/壳聚糖/ MnFeO(DNSA@CS@MnFeO)纳米光催化剂被制备出来,以在可见光下同时富集吸附和光分解。本文重点研究了 DNSA@CS 作为亚甲基蓝(MB)和 MnFeO 之间的优良连接体的重要性,在光芬顿催化试剂过氧化氢(HO)的促进下加速光降解。最佳条件为:接触时间 30min,HO 浓度 0.16M,pH 值 9,在 R.T 下用量 0.06g/l,可在 30min 内达到 98.9%的出色脱色率。更有趣的是,根据反应过程中 Mn/Mn 和 Fe/Fe 氧化还原对共存的原理,解释了混合 DNSA@CS@MnFeO 的机制。光催化脱色实验证实了 DNSA@CS@MnFeO 符合 Langmuir-Hinshelwood 模型。此外,即使经过五次运行,纳米催化系统也很稳定。所制备的纳米结构催化剂提供了简单的制造方法,促进了对 MnFeO 催化剂降解 MB 分子的机制作用标准的深入理解。

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