Khiem Ta Cong, Mao Po-Hsin, Park Young-Kwon, Duan Xiaoguang, Thanh Bui Xuan, Hu Chechia, Ghotekar Suresh, Tsang Yiu Fai, Andrew Lin Kun-Yi
Department of Environmental Engineering & Innovation and Development Center of Sustainable Agriculture, National Chung Hsing University, 250 Kuo-Kuang Road, Taichung, Taiwan.
School of Environmental Engineering, University of Seoul, Seoul, 02504, Republic of Korea.
Chemosphere. 2023 Feb;313:137309. doi: 10.1016/j.chemosphere.2022.137309. Epub 2022 Nov 26.
While Azorubin S (AZRS) is extensively used as a reddish anionic azo dye for textiles and an alimentary colorant in food, AZRS is mutagenic/carcinogenic, and it shall be removed from dye-containing wastewaters. In view of advantages of SO-related chemical oxidation technology, oxone (KHSO) would an ideal source of SO for degrading AZRS, and heterogeneous CoO-based catalysts is required and shall be developed for activating oxone. Herein, a facile protocol is proposed for fabricating mesoporous silica (MS)-confined CoO by a templating agent-mediated dry-grinding procedure. As the templating agent retained inside the ordered pores of MS (before calcination) would facilitate insertion and dispersion of Co ions into pores, the resulting CoO nanoparticles (NPs) would be grown and confined within the pores of MS after calcination, affording Co@MS. On the contrary, another analogue, Co/MS, is also prepared using the similar protocol without the templating agent-mediated introduction of Co, but CoO NPs seriously aggregate as clusters on MS. Therefore, Co@MS outperforms Co/MS for activating oxone to eliminate AZRS. Co@MS shows a noticeably lower activation energy of AZRS elimination than the existing catalysts, revealing its advantage over the reported catalysts. Moreover, the mechanistic investigation of AZRS elimination by Co@MS-activated oxone has been also elucidated for identifying the presence of SO, OH, and O in AZRS degradation using scavengers, electron paramagnetic resonance spectroscopy, and semi-quantification. The AZRS decomposition pathway is also investigated and unveiled in details via the DFT calculation. These results validate that Co@MS appears as a superior catalyst of oxone activation for AZRS degradation.
虽然偶氮玉红S(AZRS)被广泛用作纺织品的红色阴离子偶氮染料和食品中的食用色素,但AZRS具有致突变性/致癌性,应从含染料废水中去除。鉴于与SO相关的化学氧化技术的优势,过一硫酸氢钾复合盐(KHSO)将是降解AZRS的理想SO来源,并且需要开发非均相CoO基催化剂来活化过一硫酸氢钾复合盐。在此,提出了一种简便的方法,通过模板剂介导的干磨程序制备介孔二氧化硅(MS)包裹的CoO。由于保留在MS有序孔内(煅烧前)的模板剂将促进Co离子插入孔中并分散在孔中,煅烧后生成的CoO纳米颗粒(NPs)将在MS的孔内生长并受限,得到Co@MS。相反,另一种类似物Co/MS也使用类似的方法制备,没有模板剂介导的Co引入,但CoO NPs在MS上严重聚集形成团簇。因此,在活化过一硫酸氢钾复合盐以消除AZRS方面,Co@MS优于Co/MS。Co@MS显示出比现有催化剂明显更低的消除AZRS的活化能,揭示了其相对于报道催化剂的优势。此外,还阐明了Co@MS活化过一硫酸氢钾复合盐消除AZRS的机理研究,以使用清除剂、电子顺磁共振光谱和半定量来确定AZRS降解中SO、OH和O的存在。还通过密度泛函理论计算详细研究并揭示了AZRS的分解途径。这些结果证实,Co@MS是一种用于AZRS降解的过一硫酸氢钾复合盐活化的优异催化剂。