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Citation: Xue-Qin GUO, Xiao-Chuan DENG, Chao-Liang ZHU, Xin FU, Rui-Rui WANG, Wan-Xia MA, Jie FAN, Fang-Tao ZUO, Bin-Ju QING. Preparation and adsorption properties for Cs+ of modified diatomite-supported copper hexacyanoferrate composite[J]. Chinese Journal of Inorganic Chemistry, ;2023, 39(5): 815-829. doi: 10.11862/CJIC.2023.043 shu

Preparation and adsorption properties for Cs+ of modified diatomite-supported copper hexacyanoferrate composite

  • 1.

    Key Laboratory of Comprehensive and Highly Efficient Utilization of Salt Lake Resources, Qinghai Institute of Salt Lakes, Chinese Academy of Sciences, Xining 810008, China

  • 2.

    Qinghai Engineering and Technology Research Center of Comprehensive Utilization of Salt Lake Resources, Xining 810008, China

  • 3.

    University of Chinese Academy of Sciences, Beijing 100049, China

  • 4.

    Hangzhou Water Treatment Technology Development Center, Hangzhou 310012, China

  • Corresponding author: Bin-Ju QING, qbj@isl.ac.cn
  • Received Date: 18 October 2022
    Revised Date: 13 March 2023

Figures(18)

  • Herein, aluminum chloride was used as the aluminum source to modify diatomite (De) by hydrothermal method. Copper hexacyanoferrate (KCuHCF) nanoparticles were loaded onto the surface of modified De by the impregnation method, and two composite adsorbents, γ-AlOOH/De-KCuHCF and γ-Al2O3/De-KCuHCF, were prepared. The prepared materials were characterized and used for Cs+ adsorption. The results showed that the prepared adsorbents had better adsorption performance for Cs+. The maximum adsorption capacity can reach 75.44 and 84.02 mg·g-1, respectively. The desorption rate of γ-Al2O3/De-KCuHCF can reach 81.88% after three consecutive desorption with 3 mol·L-1 NH4NO3 as the desorption solution and the Cs+ adsorption rate of γ-Al2O3/De-KCuHCF in simulated brines was as high as 97.55%. After five adsorption-desorption cycles the adsorption capacity remained high. The adsorption kinetic process and adsorption isotherm model of the prepared adsorbent were also analyzed. The results showed that the adsorption process was in line with the quasi-second-order kinetic model, which was controlled by the intra-particle diffusion and liquid film diffusion, and was in line with the Langmuir adsorption isotherm model.
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