TY - JOUR
T1 - Photoinduced enhancement of 137Cs removal by NiFe Prussian blue analogue-alginate hydrogel
AU - Eun, Semin
AU - Han, Young Soo
AU - Kim, Hyuncheol
AU - Kim, Minsun
AU - Ryu, Jungho
AU - Park, Ji Hyun
AU - Lim, Jong Myoung
AU - Kim, Soonhyun
N1 - Publisher Copyright:
© 2023 Elsevier B.V.
PY - 2023/5/1
Y1 - 2023/5/1
N2 - Prussian blue analogues are promising materials for 137Cs removal; however, their use is limited by the challenge of separating them from an aqueous solution after 137Cs adsorption. This study synthesized a NiFe embedded alginate hydrogel (NiFe-AH) via cross-linking with Ni2+. The prepared NiFe-AH exhibited an excellent performance for Cs+ adsorption. The adsorption capacity of NiFe-AH under UV (0.891 mmol/g) or visible light irradiation (0.885 mmol/g) increased approximately 1.5 times more than before light irradiation (0.591 mmol/g). Moreover, the volume and weight of NiFe-AH after Cs+ adsorption decreased substantially, showing advantage in radioactive nuclide disposal. NiFe-AH exhibited high Cs+ adsorption capacity in all pH ranges, even in the presence of competing ions such as Na+, K+, Ca2+, and Mg2+. Compared to commercialized Cs+ adsorbents (AMP-PAN and KNiFe-PAN), NiFe-AH proved to have a greater Cs+ adsorption capacity. Analyses using XPS and XANES indicated that the photoinduced enhancement mechanism of Cs+ adsorption on NiFe-AH was attributed to NiFe absorbing the light, resulting in the reduction of Fe(III) to Fe(II) within NiFe. Accordingly, Cs+ ions were additionally adsorbed on NiFe. The NiFe-AH showed exceptional 137Cs removal in seawater, suggesting that it has strong potential as a practical adsorbent.
AB - Prussian blue analogues are promising materials for 137Cs removal; however, their use is limited by the challenge of separating them from an aqueous solution after 137Cs adsorption. This study synthesized a NiFe embedded alginate hydrogel (NiFe-AH) via cross-linking with Ni2+. The prepared NiFe-AH exhibited an excellent performance for Cs+ adsorption. The adsorption capacity of NiFe-AH under UV (0.891 mmol/g) or visible light irradiation (0.885 mmol/g) increased approximately 1.5 times more than before light irradiation (0.591 mmol/g). Moreover, the volume and weight of NiFe-AH after Cs+ adsorption decreased substantially, showing advantage in radioactive nuclide disposal. NiFe-AH exhibited high Cs+ adsorption capacity in all pH ranges, even in the presence of competing ions such as Na+, K+, Ca2+, and Mg2+. Compared to commercialized Cs+ adsorbents (AMP-PAN and KNiFe-PAN), NiFe-AH proved to have a greater Cs+ adsorption capacity. Analyses using XPS and XANES indicated that the photoinduced enhancement mechanism of Cs+ adsorption on NiFe-AH was attributed to NiFe absorbing the light, resulting in the reduction of Fe(III) to Fe(II) within NiFe. Accordingly, Cs+ ions were additionally adsorbed on NiFe. The NiFe-AH showed exceptional 137Cs removal in seawater, suggesting that it has strong potential as a practical adsorbent.
KW - Alginate
KW - Cs removal
KW - NiFe
KW - Photoinduced charge transfer
KW - Prussian blue analogue
UR - http://www.scopus.com/inward/record.url?scp=85148111036&partnerID=8YFLogxK
U2 - 10.1016/j.seppur.2023.123376
DO - 10.1016/j.seppur.2023.123376
M3 - Article
AN - SCOPUS:85148111036
SN - 1383-5866
VL - 312
JO - Separation and Purification Technology
JF - Separation and Purification Technology
M1 - 123376
ER -