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分散在介孔KIT-6中的CoFeO/FeO的合成、表征及光催化活性

Synthesis, Characterization and Photocatalytic Activity of CoFeO/FeO Dispersed in Mesoporous KIT-6.

作者信息

Soares Johnatan de Oliveira, Cavalcanti Wesley Eulálio Cabral, Torres Marco Antonio Morales, Pergher Sibele Berenice Castella, De Oliveira Fernando José Volpi Eusébio, Braga Tiago Pinheiro

机构信息

Instituto de Química Laboratório de Peneiras Moleculares (LABPEMOL), Instituto de Química, Universidade Federal do Rio Grande do Norte, Natal 59078-970, RN, Brazil.

Departamento de Física Teórica e Experimental, Universidade Federal do Rio Grande do Norte, Natal 59078-970, RN, Brazil.

出版信息

Nanomaterials (Basel). 2022 Oct 12;12(20):3566. doi: 10.3390/nano12203566.

Abstract

The present work aimed to synthesize and characterize a solid based on CoFeO/FeO-KIT-6 and evaluate its performance in the photocatalytic degradation of the remazol red ultra RGB dye. By analyzing XRD, N physisorption, and Mössbauer results, it was possible to identify that the desired CoFeO/FeO phase was achieved, which maintained its structural properties. The FTIR-pyridine indicated the presence of Lewis acid sites, while TPD-CO showed a large amount of weak basic sites. The band-gap energy indicated that the compound can be applied in photocatalytic degradation under UV/visible light, with the possibility of magnetic separation at the end of the reaction. The photocatalysis results indicated that there was complete degradation of the remazol red ultra RGB dye within 1 h of reaction. Despite the absence of HO, the combination of the proposed photocatalyst with the anatase phase (TiO) showed significant improvements in the degradation process. The proposed mechanism for complete dye degradation indicated that a sequence of radical reactions is necessary, generating oxidant species such as •OH and the final products were CO and HO.

摘要

本工作旨在合成并表征一种基于CoFeO/FeO-KIT-6的固体材料,并评估其在光催化降解活性艳红超RGB染料方面的性能。通过分析XRD、N物理吸附和穆斯堡尔谱结果,可以确定获得了所需的CoFeO/FeO相,且该相保持了其结构性能。FTIR-吡啶表明存在路易斯酸位点,而TPD-CO显示有大量弱碱性位点。带隙能量表明该化合物可用于紫外/可见光下的光催化降解,并且在反应结束时有可能进行磁分离。光催化结果表明,在反应1小时内活性艳红超RGB染料完全降解。尽管不存在羟基自由基,但所提出的光催化剂与锐钛矿相(TiO₂)的组合在降解过程中显示出显著的改善。所提出的染料完全降解机制表明,一系列自由基反应是必要的,会产生诸如•OH等氧化剂物种,最终产物为CO₂和H₂O。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dc0/9611405/d80702bc51e1/nanomaterials-12-03566-g001.jpg

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