In-Situ Characterization of Borate Glass Dissolution Kinetics by µ-Raman Spectroscopy
Abstract
The dissolution behavior of binary and ternary Na-Ca-borate glasses in phosphate-containing aqueous solutions was studied by micro-Raman spectroscopy. Raman spectra collected from the solutions provided information about the types and concentrations of borate anions released from the glass as a function of time. Boric acid molecules (H3BO3) and tetrahydroxyl borate anions (B(OH)4-) can be detected in solution and their relative concentrations depend on the solution pH. By monitoring the areas under peaks associated with these two species, the overall borate release rates and variations in solution pH were determined. Binary Na-borate glasses exhibit linear dissolution kinetics and the dissolution rates decrease with Na2O-contents up to 30 mol%. The ternary Na-Ca-borate glasses exhibit parabolic dissolution kinetics because of the formation of a surface Ca-phosphate phase, and these reaction rates also decrease with increasing [Na2O + CaO] content.
Recommended Citation
J. L. George and R. K. Brow, "In-Situ Characterization of Borate Glass Dissolution Kinetics by µ-Raman Spectroscopy," Journal of Non-Crystalline Solids, vol. 426, pp. 116 - 124, Elsevier B.V., Oct 2015.
The definitive version is available at https://doi.org/10.1016/j.jnoncrysol.2015.07.003
Department(s)
Materials Science and Engineering
Keywords and Phrases
Bins; Boric Acid; Calcium; Dissolution; Kinetics; Raman Spectroscopy; Reaction Kinetics; Reaction Rates; Sodium; Solutions, Borate Glass; Dissolution Behavior; Dissolution Kinetics; Dissolution Rates; In-Situ Characterization; Micro Raman Spectroscopy; Raman; Relative Concentration, Glass
International Standard Serial Number (ISSN)
0022-3093
Document Type
Article - Journal
Document Version
Citation
File Type
text
Language(s)
English
Rights
© 2015 Elsevier B.V., All rights reserved.
Publication Date
01 Oct 2015
Comments
The authors gratefully acknowledge the Center for Biomedical Science and Engineering at Missouri S&T for financial support of this research.