Transformation of Graphitic Carbon Nitride by Reactive Chlorine Species: “Weak” Oxidants Are the Main Players

石墨氮化碳 化学 纳米材料 共价键 氮化物 氮化碳 电泳剂 环境化学 无机化学 纳米技术 催化作用 材料科学 有机化学 光催化 图层(电子)
作者
Mengqiao Li,David P. Durkin,Gordon H. Waller,Yaochun Yu,Yujie Men,Tao Ye,Hanning Chen,Danmeng Shuai
出处
期刊:Environmental Science & Technology [American Chemical Society]
卷期号:57 (7): 2749-2757 被引量:6
标识
DOI:10.1021/acs.est.2c06381
摘要

Graphitic carbon nitride (g-C3N4) nanomaterials hold great promise in diverse applications; however, their stability in engineering systems and transformation in nature are largely underexplored. We evaluated the stability, aging, and environmental impact of g-C3N4 nanosheets under the attack of free chlorine and reactive chlorine species (RCS), a widely used oxidant/disinfectant and a class of ubiquitous radical species, respectively. g-C3N4 nanosheets were slowly oxidized by free chlorine even at a high concentration of 200–1200 mg L–1, but they decomposed rapidly when ClO· and/or Cl2•– were the key oxidants. Though Cl2•– and ClO· are considered weaker oxidants in previous studies due to their lower reduction potentials and slower reaction kinetics than ·OH and Cl·, our study highlighted that their electrophilic attack efficacy on g-C3N4 nanosheets was on par with ·OH and much higher than Cl·. A trace level of covalently bonded Cl (0.28–0.55 at%) was introduced to g-C3N4 nanosheets after free chlorine and RCS oxidation. Our study elucidates the environmental fate and transformation of g-C3N4 nanosheets, particularly under the oxidation of chlorine-containing species, and it also provides guidelines for designing reactive, robust, and safe nanomaterials for engineering applications.
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