Ion Exchange Behaviour of Some Amine Intercalates of α-Tin(IV) Hydrogen Phosphate Monohydrate

Author(s):  
M. J. Hudson ◽  
E. Rodriguez-Castellon ◽  
P. Sylvester
1986 ◽  
Vol 64 (1) ◽  
pp. 35-39 ◽  
Author(s):  
Rafaela Pozas-Tormo ◽  
Laureano Moreno-Real ◽  
María Martínez-Lara ◽  
Enrique Rodríguez-Castellón

The ion exchange reactions of n-butylamine intercalates of tin(IV) hydrogen phosphate and hydrogen uranyl phosphate towards carbonatotetraamminecobalt(III), chloropentaamminecobalt(III), and hexaamminecobalt(III) have been investigated. Independent of the complex cation charges, the amounts of Co(III) complex exchanged by the n-butylamine intercalate of tin(IV) hydrogen phosphate are practically the same. With the n-butylamine intercalate of hydrogen uranyl phosphate, the ionic exchange was completed and the composition was fixed by the exchanged Co(III) complex. The layer charge densities of these phosphates justify the different ionic exchange behaviour observed towards the large complex cations. All the products were characterized by chemical analysis, X-ray diffractometry, infrared spectroscopy, diffuse reflectance spectroscopy, and thermal analysis.


1990 ◽  
Vol 24 (1) ◽  
pp. 77-88 ◽  
Author(s):  
M.J. Hudson ◽  
E. Rodriguez-Castellon ◽  
P. Sylvester ◽  
A. Jimenez-Lopez ◽  
P. Olivera-Pastor

1995 ◽  
Vol 13 (6) ◽  
pp. 1145-1158 ◽  
Author(s):  
H. Hayashi ◽  
T. Iwasaki ◽  
T. Nagase ◽  
Y. Onodera ◽  
K. Torii

1989 ◽  
Vol 120 (12) ◽  
pp. 1091-1094 ◽  
Author(s):  
Eshrat Fakhari ◽  
Thomas Sch�nfeld

1982 ◽  
Vol 35 (7) ◽  
pp. 1335 ◽  
Author(s):  
M Chatterjee ◽  
D Ganguli

The exchange behaviour of some divalent transition metal ions M2+ (Zn2+, Cu2+, Ni2+, Co2+, Mn2+) in a zeolite NaX (SiO2/Al2O3 2.75) was studied at intermediate stages before equilibrium. The equivalent counter ion supply in the solution, given by the equivalent ratio of the two counter ions 2M2+/Na+, was found to be critical in determining the saturation level of exchange. The series of relative abilities of exchange was very similar to the well known selectivity series at equilibrium. It is suggested that water exchange of the metal ions in solution could be one of the factors controlling the relative ease of ion exchange.


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