Effect of Treatment of Synthetic Zeolite-Polymer Membranes on Their Electrochemical-Potential Response Characteristics
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Evmiridis, N. P.
Demertzis, M. A.
Vlessidis, A. G.
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Springer Verlag (Germany)
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peer reviewed
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Fresenius Journal of Analytical Chemistry
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The performance of synthetic-polymer membrane-electrodes for cation sensing is investigated by obtaining E versus pM graphs and E versus time curves of the same membrane type under different treatments or of membranes constructed by modified procedures. The slopes of E versus pM curves for the salts of monovalent cations show different values for the same membrane type as well as for the different membrane types and are found within the range of 43 to 57 mV per pM. The response time of the membrane is found to be slower when the membranes are plastic phase deficient. Generally, the detection limit is only slightly dependent on the composition of the membrane and the best value is obtained with the polished membranes which is close to the value of pM = 5 while for the other membranes the values are within the range of pM 4 to 5. The range of linearity is also slightly dependent on the method of membrane construction and in general is shorter when the membranes are plastic phase deficient. The selectivity coefficients are found to depend significantly on the method of construction of the membrane but in general the selectivity of all the membranes studied in this report is poor. The asymmetry potential is found to be related to an ion exchange process and is developed slowly in 5A-type membranes. However, when the value of asymmetry potential is high, a longer time is needed to reach the final value of e.m.f. in measurements among different concentrations of the same metal ion and much longer is needed where there is switching of measurement from a monovalent cation to a divalent cation.
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electrode
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<Go to ISI>://A1991FQ22000003
http://download.springer.com/static/pdf/998/art%253A10.1007%252FBF00324470.pdf?auth66=1381994501_363a6b0d2920ce8a56a24f1514221a5d&ext=.pdf
http://download.springer.com/static/pdf/998/art%253A10.1007%252FBF00324470.pdf?auth66=1381994501_363a6b0d2920ce8a56a24f1514221a5d&ext=.pdf
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en
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Πανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείας