光催化
兴奋剂
煅烧
铀
热液循环
材料科学
氧化还原
X射线光电子能谱
食腐动物
甲醇
无机化学
核化学
化学工程
冶金
化学
光电子学
激进的
催化作用
生物化学
工程类
有机化学
作者
Mingyu Xie,Qi Liu,Jingyuan Liu,Jing Yu,Rongrong Chen,Jiahui Zhu,Rumin Li,Jun Wang
标识
DOI:10.1016/j.seppur.2024.127338
摘要
The Cu-doped SrTiO3 photocatalysts were prepared by hydrothermal and calcination methods for photocatalytic reduction of U(VI) in mine pit water. Specifically, Cu doping decreases the bandgap of the catalyst, broadening the light absorption spectrum and accelerating photo-induced charge carrier separation. Consequently, these modifications significantly enhance the performance of photocatalytic uranium reduction. With methanol as a hole scavenger, the removal rate of U(VI) in 100 mg/L simulated pit water was 89.4 %. When there is no hole scavenger, the photocatalyst still achieves a 71.3 % uranium removal rate in actual mine pit water (25 mg/L). In addition, the photocatalyst has a certain degradation effect on the natural organic matter (NOM) in the actual mine water. XPS analysis reveals that uranium reduction involves Ti(III)/Ti(IV) and Cu(I)/Cu(II) redox processes. The redox processes of these metals may enhance the reducing properties of photocatalysts. This study presents a new method for large-scale mine pit water treatment via Cu-doped SrTiO3 photocatalysts.
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