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Co(OH)/CuO协同催化可见光照射下有机污染物的降解

Synergistic Catalysis of Co(OH)/CuO for the Degradation of Organic Pollutant Under Visible Light Irradiation.

作者信息

Akram Naeem, Guo Jia, Ma Wenlan, Guo Yuan, Hassan Afaq, Wang Jide

机构信息

Key Laboratory of Oil and Gas Fine Chemicals, Ministry of Education & Xinjiang Uygur Autonomous Region, College of Chemistry and Chemical Engineering, Xinjiang University, Urumqi, 830046, China.

出版信息

Sci Rep. 2020 Feb 6;10(1):1939. doi: 10.1038/s41598-020-59053-9.

Abstract

The exploration of advanced water treatment technologies e.g. heterogeneous photocatalysis is the most promising way to address organic pollution issues. Semiconductors based bimetallic photocatalysis with wide bandgap, have displayed splendid degradation performance in the UV light region, but their extension to the visible light/near infra-red region is still a matter of great concern. CuO, Co(OH), CoO and Co(OH)/CuO nanocomposites were synthesized via simple co-precipitation method and further practiced for Rhodamine B (RhB) decomposition by introducing per-sulfate (PS) as a sacrificial agent. Results revealed that Co(OH)/CuO catalyst had shown robust catalytic activity for RhB photodegradation (degradation time 8 min, k = 0.864 min) under light illumination, significantly less (12-60 times) than the other reported bimetallic catalysts. Catalyst also have verified excellent performance for a broader pH range (5-9) with excellent stability. Main reactive species responsible for the photocatalytic reaction were sulfate (SO) and superoxide (O) radicals, duly verified by ESR and by using radical scavengers. With outstanding recycling abilities, this is probably the fewer successful attempt for RhB decolorization and can be highly favorable for effluent treatment by using the synergic effect of absorption and photodegradation.

摘要

探索先进的水处理技术,如多相光催化,是解决有机污染问题最有前景的方法。基于宽带隙半导体的双金属光催化在紫外光区域表现出出色的降解性能,但其向可见光/近红外区域的扩展仍然是一个备受关注的问题。通过简单的共沉淀法合成了CuO、Co(OH)、CoO和Co(OH)/CuO纳米复合材料,并通过引入过硫酸盐(PS)作为牺牲剂进一步用于罗丹明B(RhB)的分解。结果表明,Co(OH)/CuO催化剂在光照下对RhB光降解表现出强大的催化活性(降解时间8分钟,k = 0.864分钟),明显少于其他报道的双金属催化剂(少12 - 60倍)。该催化剂在较宽的pH范围(5 - 9)内也表现出优异的性能和稳定性。通过电子顺磁共振(ESR)和使用自由基清除剂, duly验证了光催化反应的主要活性物种是硫酸根(SO)和超氧根(O)自由基。由于具有出色的循环能力,这可能是较少的成功实现RhB脱色的尝试之一,并且利用吸收和光降解的协同效应,对废水处理非常有利。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/394f/7005304/8029e4226907/41598_2020_59053_Fig1_HTML.jpg

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