4.7 Article

Nanofabricated chitosan/graphene oxide electrodes for enhancing electrosorptive removal of U(VI) from aqueous solution

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ELSEVIER
DOI: 10.1016/j.seppur.2022.120827

关键词

Chitosan; Graphene oxide; Uranium; Electrosorption

资金

  1. Natural Science Foundation of China [22176032, 21866002, 22068002]
  2. Key Project of Natural Science Foundation of Jiangxi [20212BAB203023]
  3. Training Plan Project of Academic and Technical Leaders of Major Disciplines in Jiangxi [20212BCJ23001]

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In this study, chitosan/graphene oxide (CS/GO) nano-electrodes were fabricated for the efficient electrosorption of U(VI) from uranium-containing effluents. The CS/GO-4 electrode showed the best electrosorption performance for U(VI) due to its well-balanced meso-/micro-porous structure and superior conductivity. The isotherms and kinetics were fitted by Langmuir model. The maximum removal capacity for U(VI) reached 271.2 mg/g at 0.9 V, which was almost double compared to 0.0 V. The electrosorption-desorption cycles further demonstrated the potential application of CS/GO electrode materials for the removal of U(VI) from radioactive wastewater.
The radioactive pollution caused by uranium-containing effluents brings serious detriments to environmental safety and human health. Herein the chitosan/graphene oxide (CS/GO) electrodes were nano-fabricated for the effective electrosorption of U(VI) from aqueous solution. The cyclic voltammetry measurements were conducted to determine the specific capacitance of the CS/GO materials. The U(VI) electrosorption was performed on capacitive deionization (CDI) system. The results showed that CS/GO-4 presented best electrosorption performance for U(VI) among various CS/GO materials, which is associated with a well-balanced meso-/micro-porous structure for promoting ion transfer and superior conductivity for ion trapping through electrical double-layer (EDL) interaction. The isotherms could be described by Langmuir model, whereas the kinetics could be fitted by Langmuir model. The maximum removal capacity for U(VI) electrosorption by CS/GO-4 reached 271.2 mg/g at 0.9 V, which was almost double that achieved at 0.0 V. The electrosorption mechanism may involve in the formation of electrical double-layer (EDL) and the coordination of U(VI) by the amine and carboxyl groups of CS/ GO materials. The electrosorption-desorption cycles further demonstrated that the potential application of CS/ GO electrode materials for the electrosorptive removal of U(VI) from radioactive wastewater.

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