Applied Catalysis B: Environment and Energy ( IF 20.2 ) Pub Date : 2023-03-12 , DOI: 10.1016/j.apcatb.2023.122619 Minzi Liao , Shengxi Zhao , Kai Wei , Hongwei Sun , Lizhi Zhang
Cr(III)-organic complexes removal from wastewater is challenging to decompose the complexes without producing toxic Cr(VI). Herein we demonstrated that oxalated zero-valent iron (Ox-ZVI) could one-step decomplex 95.4% of Cr(III)-EDTA with 94.2% removal of total Cr and 60.5% removal of TOC without generating Cr(VI) at pH 6.0. Ox-ZVI with FeC2O4 shell preferred to adsorb and activate O2 to produce more reactive species than ZVI with iron oxide shell, while the generated 1O2 could selectively break the Cr-O and Cr-N bond to precisely decomplex Cr(III)-EDTA without producing Cr(VI). The released Cr(III) was in-situ precipitated on the surface of ZVI in Cr(OH)3 form. Interestingly, •OH preferred the effective degradation of the released EDTA ligand to the oxidation of the chelated Cr(III) at pH 6.0. This study offers a green and facile method for the Cr(III)-organic complexes treatment, and also sheds light on the importance of reactive species adjustment for the precise pollutant control.
中文翻译:
Cr(III)-EDTA 的精确解络和草酸零价铁原位 Cr(III) 去除
从废水中去除 Cr(III)-有机络合物对于分解络合物而不产生有毒的 Cr(VI) 具有挑战性。在本文中,我们证明了草酸零价铁 (Ox-ZVI) 可以在 pH 6.0 下一步解络 95.4% 的 Cr(III)-EDTA,同时去除 94.2% 的总 Cr 和 60.5% 的 TOC 而不会产生 Cr(VI) . 具有FeC 2 O 4壳的Ox-ZVI比具有氧化铁壳的ZVI更倾向于吸附和活化O 2以产生更多的活性物质,而生成的1 O 2可以选择性地破坏Cr-O和Cr-N键以精确解络Cr (III)-EDTA 不产生 Cr(VI)。释放的 Cr(III) 在 Cr(OH) 3中原位沉淀在 ZVI 表面形式。有趣的是,在 pH 6.0 下,•OH 更喜欢释放的 EDTA 配体的有效降解,而不是螯合的 Cr(III) 的氧化。本研究为 Cr(III)-有机络合物的处理提供了一种绿色简便的方法,同时也阐明了活性物种调节对于精确控制污染物的重要性。