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Effects of magnesium content on the physical, chemical and degradation properties in a MgO−CaO−Na2O−P2O5 glass system
This paper presents the structural characterisation and degradation behavior of the glass system 20Na2O–(30−X)CaO–XMgO–50P2O5 (X=0, 5, 10, 15, 20, 25 and 30mol%) wherein magnesium oxide is introduced as a partial calcium oxide substitute. This system is of interest from the viewpoint of investigatin...
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Published in: | Journal of non-crystalline solids 2013-03, Vol.363, p.57-63 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | This paper presents the structural characterisation and degradation behavior of the glass system 20Na2O–(30−X)CaO–XMgO–50P2O5 (X=0, 5, 10, 15, 20, 25 and 30mol%) wherein magnesium oxide is introduced as a partial calcium oxide substitute. This system is of interest from the viewpoint of investigating the subtle effects on structure and degradation that arise from the substitution of divalent ions (Mg2+ for Ca2+) in these glass systems. Studies such as differential thermal analysis (DTA), Fourier transform infrared (FTIR) spectroscopy and 31P nuclear magnetic resonance (NMR) reveal little change in the glass structure. However, degradation and ion release measurements for glass discs immersed in deionised water at 37°C over a 21day period highlight an inverse exponential effect between glass degradation rate and MgO content. Thus, the investigated glass systems provide interesting insights into the effects of parameters such as ionic radius, atomic weight and bond length on the glass properties. From an applications perspective, these glasses offer a selective range of degradation rates from highly degradable to relatively stable systems and can potentially serve as vehicles for the delivery of magnesium ions in the clinical realm.
► Substitution of CaO with MgO allows control of the degradation and pH changes. ► The change in degradation and pH is more strongly influenced by ionic size than by ionic charge. ► No change in surface energy properties may be seen. |
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ISSN: | 0022-3093 1873-4812 |
DOI: | 10.1016/j.jnoncrysol.2012.11.036 |