2019
DOI: 10.1039/c8ra09386e
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Amino-functionalized magnetic chitosan beads to enhance immobilization of potassium copper hexacyanoferrate for selective Cs+ removal and facile recovery

Abstract: The magnetic chitosan beads were amino-functionalized by grafting and showed an outstanding removal performance for radioactive Cs+.

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Cited by 27 publications
(6 citation statements)
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“…Hexacyanoferrates (HCFs) of various transition metals have once again begun to attract attention as sorbents in the selective extraction of Cs + ions. 1,2,3,4,5,6,7,8,9,10 This is due to their high sorption capacity for caesium over a wide pH range, in high salinity, and their high stability. 11,12,13,14,15 In case of K-Hexacyanoferrates of transition metals, and especially Cu-HCF, the Cs + sorption mechanism occurs via an ionic exchange between K + from the solid structure and Cs + from the solution.…”
Section: Introductionmentioning
confidence: 99%
“…Hexacyanoferrates (HCFs) of various transition metals have once again begun to attract attention as sorbents in the selective extraction of Cs + ions. 1,2,3,4,5,6,7,8,9,10 This is due to their high sorption capacity for caesium over a wide pH range, in high salinity, and their high stability. 11,12,13,14,15 In case of K-Hexacyanoferrates of transition metals, and especially Cu-HCF, the Cs + sorption mechanism occurs via an ionic exchange between K + from the solid structure and Cs + from the solution.…”
Section: Introductionmentioning
confidence: 99%
“… 42 . The XRD pattern of chitosan appeared as one broad peak at 19.87° 43 confirm the amorphous structure of chitosan as the occurrence of broad peak at 20.1°. In the MchiBs spectrum, all-characteristic peaks of pure magnetite and chitosan appeared in Fig.…”
Section: Characterizationmentioning
confidence: 53%
“…FT-IR spectrum of CMC ( Figure 4 b) exhibited broad bands at 3300–3500 cm −1 , 1422 and 1607, and 1000 and 1200 cm −1 , which were assigned to the stretching of -OH groups, symmetrical and asymmetrical stretching vibrations of the COO– groups and –C–O stretching on the polysaccharide skeleton, respectively [ 4 , 39 ]. All the bands were present in CMC/CuO-Co 2 O 3 ( Figure 4 c), while for chitosan coating beads Cs@CMC/CuO-Co 2 O 3 ( Figure 4 d) new bands at 1155 and 1654 cm −1 appeared, which were attributed to the saccharide and (–NH 2 ) amine group in chitosan polymer [ 40 ]. All the peaks that appeared in the Ni/Cs@ CMC/CuO-Co 2 O 3 beads are clearly seen in Figure 4 e.…”
Section: Resultsmentioning
confidence: 99%