TY - JOUR
T1 - Hydrous protonated forms derived from n=3 Dion-Jacobson-type layered perovskite titanotantalate RbLa2Ti2TaO10
T2 - Interlayer reactivity with n-alkylamine
AU - Matsuda, Motohide
AU - Hioki, Toshifumi
AU - Okada, Keisuke
AU - Nishimoto, Shunsuke
AU - Miyake, Michihiro
PY - 2006/5
Y1 - 2006/5
N2 - Hydrous protonated forms of layered perovskite titanotantalate were derived from the n=3 Dion-Jacobson-type RbLa2Ti2TaO10 by ion-exchange of the interlayer Rb+ ions in aqueous HNO3, and their interlayer reactivity with n-alkylamine was investigated. Although all of the protonated forms thus derived were indexed as the same tetragonal cell with P4/mmm as the host, the interlayer reactivity with n-alkylamine was degraded with an increase in the ion-exchange treatment time. A significant difference was observed in dehydration behavior below 200 °C. The protonated forms synthesized with short ion-exchange time showed a large endothermic peak with weight loss around 60 °C, while those with prolonged treatment time did not. The intercalation of n-alkylamine was confirmed for the former, but not for the latter. From these results, it was considered that hydronium ions and/or H2O molecules responsible for the dehydration around 60 °C play an important role in the intercalation of n-alkylamine into the protonated forms.
AB - Hydrous protonated forms of layered perovskite titanotantalate were derived from the n=3 Dion-Jacobson-type RbLa2Ti2TaO10 by ion-exchange of the interlayer Rb+ ions in aqueous HNO3, and their interlayer reactivity with n-alkylamine was investigated. Although all of the protonated forms thus derived were indexed as the same tetragonal cell with P4/mmm as the host, the interlayer reactivity with n-alkylamine was degraded with an increase in the ion-exchange treatment time. A significant difference was observed in dehydration behavior below 200 °C. The protonated forms synthesized with short ion-exchange time showed a large endothermic peak with weight loss around 60 °C, while those with prolonged treatment time did not. The intercalation of n-alkylamine was confirmed for the former, but not for the latter. From these results, it was considered that hydronium ions and/or H2O molecules responsible for the dehydration around 60 °C play an important role in the intercalation of n-alkylamine into the protonated forms.
KW - A. Ceramics
KW - B. Chemical synthesis
KW - C. Thermogravimetric analysis (TGA)
KW - D. Crystal structure
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U2 - 10.1016/j.jpcs.2006.01.065
DO - 10.1016/j.jpcs.2006.01.065
M3 - Article
AN - SCOPUS:33744908857
SN - 0022-3697
VL - 67
SP - 1325
EP - 1329
JO - Journal of Physics and Chemistry of Solids
JF - Journal of Physics and Chemistry of Solids
IS - 5-6
ER -