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Carbene ligand-doped fe2 o3 composite for rapid removal of multiple dyes under sunlight

journal contribution
posted on 2024-11-02, 18:55 authored by Siwei Yang, Yichao Zhuang, Yuanfang Shen, Weihang Han, Liangchen Chen, Qiang SunQiang Sun, Di Wu, Hui Zheng
Contaminated water due to industrial organic dyes presents a significant challenge to sustainability. As a material of green energy, photocatalysts offer an effective and environmentally friendly way to deal with organic dyes for water treatment. A series of simple and highly efficient iron photocatalysts with carbene ligands were developed, which, under the illumination of sunlight, can rapidly degrade multiple organic dyes in water at room temperature, including rhodamine B (RhB), indigo carmine (IC), methyl blue (MB), and congo red (CR). The field-only surface integral method was carried out to determine the absorption spectrum of photocatalyst particles. Under the optimized experimental conditions which were selected by the orthogonal experiments for four dyes, 0.5a@Fe2 O3 and 2c@Fe2 O3 demonstrated good stability and photocatalytic activity. These two composite materials not only have the ability to remove 98.0% of the degradation in 10 s, but also maintain high reactivity after a few cycles of repeated use.

Funding

ARC Centre of Excellence for Nanoscale BioPhotonics

Australian Research Council

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Robust methods for solving integral equations in science and engineering

Australian Research Council

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History

Related Materials

  1. 1.
    DOI - Is published in 10.3390/su132212669
  2. 2.
    ISSN - Is published in 20711050

Journal

Sustainability

Volume

13

Number

12669

Issue

22

Start page

1

End page

14

Total pages

14

Publisher

MDPIAG

Place published

Switzerland

Language

English

Copyright

Copyright: © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https:// creativecommons.org/licenses/by/ 4.0/).

Former Identifier

2006112668

Esploro creation date

2022-03-24