Supporting of Potassium Copper Hexacyanoferrate on Porous Activated Carbon Substrate for Cesium Separation

被引:34
|
作者
Wang, Li [1 ]
Feng, Miao [1 ]
Liu, Chunxia [1 ]
Zhao, Yongsheng [1 ]
Li, Shuqiong [1 ]
Wang, Hang [1 ]
Yan, Liang [1 ]
Tian, Gan [1 ]
Li, Shoujian [1 ]
机构
[1] Sichuan Univ, Coll Chem, Chengdu 610064, Peoples R China
基金
中国国家自然科学基金;
关键词
Activated carbon; cesium; hexacyanoferrate; inorganic ion exchanger; separation; ION-EXCHANGE; COBALT HEXACYANOFERRATE; SORPTION MECHANISMS; SELECTIVE SORPTION; CS ION; REMOVAL; ZEOLITES; WASTE; COMPOSITES; DIFFUSION;
D O I
10.1080/01496390903183253
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Activated carbon (AC) was chosen for carrying potassium copper hexacyanoferrate (KCuCF) to prepare a new Cs-selective material. The adsorbent was prepared by repetitious batch precipitation reaction of Cu2+ with [Fe(CN)6]4-. Characterization analyses identified the backbone formula of the activated carbon-supported KCuCF with K2Cu[Fe(CN)6], and shown the successful loading of KCuCF microcrystals on the porous carbon substrate with a loading percentage of 12.5wt%, and with BET specific surface area and a total pore volume of 527.8m2/g and 0.38cm3/g for AC and 160.8m2/g and 0.16cm3/g for KCuCF-loaded activated carbon (KCuCF-AC), respectively. The optimal Cs adsorption capacity of about 0.46mmol center dot g-1 was observed between the HNO3 concentration of 0.5-1.5M, and the capacity even reached to 0.38mmol center dot g-1 in the presence of a large amount of competing cations. The results indicate that activated carbon has no significant effect on the selectivity of the as-synthesized composite.
引用
收藏
页码:4023 / 4035
页数:13
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