TY - JOUR
T1 - Immobilization of cesium in fly ash-silica fume based geopolymers with different Si/Al molar ratios
AU - Tian, Quanzhi
AU - Nakama, Shingo
AU - Sasaki, Keiko
N1 - Funding Information:
This research was supported to KS by the JSPS (Japan Society for the Promotion of Science) Kaken Kiban A project (No. JP16H02435 ) and to TQ by the China Scholarship Council (No. 201706420068 ).
Publisher Copyright:
© 2019 Elsevier B.V.
PY - 2019/10/15
Y1 - 2019/10/15
N2 - Geopolymers are considered as promising matrixes for waste solidification. However, the effects of the Si/Al molar ratio of geopolymer on the immobilization efficiencies for metal ions have not been fully studied and understood. In the present study, geopolymers with different Si/Al ratios were synthesized from coal fly ash and silica fume. Adsorption tests were conducted to evaluate their immobilization efficiencies for Cs+. The results indicated that geopolymer with low Si/Al ratio could have a better immobilization performance for Cs+ than that with high Si/Al ratio. High Si/Al ratio could contribute to a more compact structure of geopolymer. Each sorption process fitted better with the pseudo-second-order model, and all of them were governed by film diffusion. However, the diffusion mode was gradually closed to particle diffusion with the increase in the Si/Al ratio. Both Langmuir and Freundlich models could well fit the sorption data, and the free energy of each sorption process decreased with the increase in the Si/Al ratio according to D-R equation. The distribution of AlO4 tetrahedron in the geopolymer structure plays a significant role in the immobilization of Cs+. Low Si/Al ratio could result in that more AlO4 tetrahedrons distribute in the small rings (+. However, high Si/Al ratio leads to the distribution of AlO4 tetrahedrons mainly in larger rings (≥eight-member), and this could contribute to the high leaching amount of Cs+. In addition, high-temperature treatment could contribute to the formation of nepheline or pollucite in geopolymer matrix. These minerals locked Cs+ in their structures, and the leaching amount of Cs+ was reduced correspondingly from high levels (26.36%, 27.26%, and 66.92%) to very low levels (0.67%, 0.53%, and 0.95%).
AB - Geopolymers are considered as promising matrixes for waste solidification. However, the effects of the Si/Al molar ratio of geopolymer on the immobilization efficiencies for metal ions have not been fully studied and understood. In the present study, geopolymers with different Si/Al ratios were synthesized from coal fly ash and silica fume. Adsorption tests were conducted to evaluate their immobilization efficiencies for Cs+. The results indicated that geopolymer with low Si/Al ratio could have a better immobilization performance for Cs+ than that with high Si/Al ratio. High Si/Al ratio could contribute to a more compact structure of geopolymer. Each sorption process fitted better with the pseudo-second-order model, and all of them were governed by film diffusion. However, the diffusion mode was gradually closed to particle diffusion with the increase in the Si/Al ratio. Both Langmuir and Freundlich models could well fit the sorption data, and the free energy of each sorption process decreased with the increase in the Si/Al ratio according to D-R equation. The distribution of AlO4 tetrahedron in the geopolymer structure plays a significant role in the immobilization of Cs+. Low Si/Al ratio could result in that more AlO4 tetrahedrons distribute in the small rings (+. However, high Si/Al ratio leads to the distribution of AlO4 tetrahedrons mainly in larger rings (≥eight-member), and this could contribute to the high leaching amount of Cs+. In addition, high-temperature treatment could contribute to the formation of nepheline or pollucite in geopolymer matrix. These minerals locked Cs+ in their structures, and the leaching amount of Cs+ was reduced correspondingly from high levels (26.36%, 27.26%, and 66.92%) to very low levels (0.67%, 0.53%, and 0.95%).
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U2 - 10.1016/j.scitotenv.2019.06.095
DO - 10.1016/j.scitotenv.2019.06.095
M3 - Article
C2 - 31412449
AN - SCOPUS:85067421427
SN - 0048-9697
VL - 687
SP - 1127
EP - 1137
JO - Science of the Total Environment
JF - Science of the Total Environment
ER -