Apatite Thermochemistry: the Simple Salt Approximation
Drouet has recently comprehensively reviewed the thermochemistry of phosphate apatites, M10(PO4)6X2. On the basis of the data assembled, he has established an optimized additive set of data values based upon the component ions, M2+, P2O5, or PO43–, and halide or OH– ions, which yield phosphoapatite...
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| Format: | Journal Article |
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American Chemical Society
2019
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| Online Access: | http://hdl.handle.net/20.500.11937/76416 |
| _version_ | 1848763683855925248 |
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| author | Glasser, Leslie |
| author_facet | Glasser, Leslie |
| author_sort | Glasser, Leslie |
| building | Curtin Institutional Repository |
| collection | Online Access |
| description | Drouet has recently comprehensively reviewed the thermochemistry of phosphate apatites, M10(PO4)6X2. On the basis of the data assembled, he has established an optimized additive set of data values based upon the component ions, M2+, P2O5, or PO43–, and halide or OH– ions, which yield phosphoapatite enthalpy and Gibbs energy values generally within 1% of their experimental values. In this paper, we introduce and compare the Simple Salt Approximation (SSA) for generation of the same thermodynamic values by addition of values for the component salts of the apatite. SSA is widely applicable to ionic systems so that familiarity with this procedure is worthwhile. Drouet’s additive values focused on phosphoapatites yield better results (at 1%) than does the more general SSA (at ∼3%), but the SSA provides an alternative to data prediction when the Drouet additive factors are not available. In addition, we here use the SSA to generate approximate entropy values and estimate the Debye temperature of phosphoapatites under ambient conditions, yielding insight into the extent of activation of their vibrational modes. |
| first_indexed | 2025-11-14T11:07:22Z |
| format | Journal Article |
| id | curtin-20.500.11937-76416 |
| institution | Curtin University Malaysia |
| institution_category | Local University |
| last_indexed | 2025-11-14T11:07:22Z |
| publishDate | 2019 |
| publisher | American Chemical Society |
| recordtype | eprints |
| repository_type | Digital Repository |
| spelling | curtin-20.500.11937-764162019-10-03T07:48:48Z Apatite Thermochemistry: the Simple Salt Approximation Glasser, Leslie Drouet has recently comprehensively reviewed the thermochemistry of phosphate apatites, M10(PO4)6X2. On the basis of the data assembled, he has established an optimized additive set of data values based upon the component ions, M2+, P2O5, or PO43–, and halide or OH– ions, which yield phosphoapatite enthalpy and Gibbs energy values generally within 1% of their experimental values. In this paper, we introduce and compare the Simple Salt Approximation (SSA) for generation of the same thermodynamic values by addition of values for the component salts of the apatite. SSA is widely applicable to ionic systems so that familiarity with this procedure is worthwhile. Drouet’s additive values focused on phosphoapatites yield better results (at 1%) than does the more general SSA (at ∼3%), but the SSA provides an alternative to data prediction when the Drouet additive factors are not available. In addition, we here use the SSA to generate approximate entropy values and estimate the Debye temperature of phosphoapatites under ambient conditions, yielding insight into the extent of activation of their vibrational modes. 2019 Journal Article http://hdl.handle.net/20.500.11937/76416 10.1021/acs.inorgchem.9b02343 American Chemical Society restricted |
| spellingShingle | Glasser, Leslie Apatite Thermochemistry: the Simple Salt Approximation |
| title | Apatite Thermochemistry: the Simple Salt Approximation |
| title_full | Apatite Thermochemistry: the Simple Salt Approximation |
| title_fullStr | Apatite Thermochemistry: the Simple Salt Approximation |
| title_full_unstemmed | Apatite Thermochemistry: the Simple Salt Approximation |
| title_short | Apatite Thermochemistry: the Simple Salt Approximation |
| title_sort | apatite thermochemistry: the simple salt approximation |
| url | http://hdl.handle.net/20.500.11937/76416 |