The effects of time, temperature, and concentration on Sr2+ exchange in clinoptilolite in aqueous solutions
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Jennifer L. Palmer
Abstract
Four grams of a clinoptilolite-rich rock, crushed to -180 mesh, were exchanged in deionized water (DI), and in 0.1, 0.01, and 0.001 M solutions of SrCl2·6H2O at 5, 21, 50, and 90 °C for 0.5, 5, 24, and 240 h yielding 64 sample solutions, which were vacuum-filtered to remove solids. The solutions were analyzed by ICP-AES for the outgoing cations (i.e., Na+, K+, Ca2+, and Mg2+). The higher molarity solutions were expected to contain greater concentrations of the outgoing cations than the DI or lower molarity concentration solutions. This trend was exhibited by the monovalent and divalent cations in samples of all concentrations. Outgoing monovalent cations exchanged to greater extents with increasing time and temperature. Outgoing divalent cations of 0.01 and 0.001 M concentrations exchanged at low temperatures contained greater concentrations of outgoing divalent cations than solutions exchanged at high temperatures. The concentrations of the monovalent cations were slightly greater in the 0.001 M sample than in DI, whereas divalent cations had a similar concentration between the 0.001 M and DI treatments. Overall exchange of cations out of the clinoptilolite was favored at higher temperatures.
© 2015 by Walter de Gruyter Berlin/Boston
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- Thermodynamics of ion-exchanged and natural clinoptilolite
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- Fe3+/ΣFe vs. FeLα peak energy for minerals and glasses: Recent advances with the electron microprobe
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- The nature of radiohaloes in biotite: Experimental studies and modeling
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