2003
DOI: 10.1016/s0167-2738(03)00229-7
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Cation mobility and ion exchange in acid tin phosphate

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Cited by 16 publications
(13 citation statements)
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“…They have attributed this behaviour to the strong H-bonds in acid tin phosphate resulting in a higher energy requirements for proton jumps from one site to another. 21 Similar explanation can also be extended in case of SnP in the present study.…”
supporting
confidence: 84%
See 1 more Smart Citation
“…They have attributed this behaviour to the strong H-bonds in acid tin phosphate resulting in a higher energy requirements for proton jumps from one site to another. 21 Similar explanation can also be extended in case of SnP in the present study.…”
supporting
confidence: 84%
“…Stenina and coworkers have reported the conduction behaviour of tin phosphate. 21 Literature survey reveals that most of the proton transport properties carried out in case of zirconium phosphate and titanium phosphate have been on crystalline phases and not many reports exist in the case of tin phosphate. We therefore considered it worth while to study the proton transport properties of amorphous M(IV) phosphates, where M(IV) = Zr, Sn and Ti abbreviated as ZrP, SnP and TiP respectively, and compare their proton conduction behaviour.…”
Section: Introductionmentioning
confidence: 99%
“…5a, b, c. In the present study, E a values in kcal mol -1 , follow the order ZrHEDP (13.20) > ZTHEDP (11.13) > TiHEDP (2.87), however, the specific conductance values follow the order ZTHEDP > ZrHEDP > TiHEDP. High E a and high conductance values have also been observed previously by us and other researchers [16,20]. Lower E a values indicate ease of conduction and suggest the mechanism to be Grotthuss type, where E a entirely depends on reorientation of water molecules on the surface which has been explained earlier in the text.…”
Section: Impedance Measurementssupporting
confidence: 83%
“…E a values depend on several factors such as high density of mobile ions, the availability of vacant sites, good connectivity among the sites, complexity in structure/steric effect, acidity (charge to size ratio) of the metal ion and hydrogen bonding resulting in a higher energy requirement for proton jump from one site to another [19,20]. The observed E a is a result of the contribution of the above-mentioned factors.…”
Section: Impedance Measurementsmentioning
confidence: 99%
“…It is also reported that the conductivity varies linearly with the number of surface phosphate groups [19]. The mechanism of diffusion and proton transport in crystalline zirconium phosphate (ZP), titanium phosphate (TP), tin phosphate, tantalum phosphate, uranyl phosphate have been studied in detail by various workers [19][20][21][22][23][24][25][26][27][28][29]. From our laboratory, we have reported proton transport properties of M(IV) tungstates and phosphates, where M(IV) = Zr, Sn, Ti [30,31].…”
Section: Introductionmentioning
confidence: 99%