FeLaO3: enthalpy of formation
4 accepted literature formation-enthalpy value(s) (experimental 3, model 1); experimental median -270.818 kJ/mol-atom (n = 2).
Systems: Fe–La–O
Literature values
| Value | Phase as printed | T (K) | Class | Method | System | Source | Location | Quote |
|---|---|---|---|---|---|---|---|---|
| -1373.48 kJ/mol (basis unstated) ± 2.61 | LaFeO3 | 298.15 | experimental | drop solution calorimetry | Fe–La–O | [1] Povoden-Karadeniz 2009 cites Cheng 2005 doi | Table 1, p. 4, row 2 report | |
| -274.696 kJ/mol-atom ± 0.522 | LaFeO3 | 298.15 | experimental | drop solution calorimetry | Fe–La–O | [1] Povoden-Karadeniz 2009 cites Cheng 2005 doi | Table 1, p. 4, row 2 report | |
| -266.94 kJ/mol-atom | LaFeO3 | 298.15 | experimental | Calvet microcalorimetry | Fe–La–O | [1] Povoden-Karadeniz 2009 cites Parida 1998 doi | Table 1, p. 4, row 3 report | |
| -273.64 kJ/mol-atom | LaFeO3 | 298.15 | model | Fe–La–O | [1] Povoden-Karadeniz 2009 | Table 1, p. 4, row 1 report |
Uncertainty budget
Components kept separate, in the value's unit (literature SCHEMA.md, UNCERTAINTY_CALIBRATION.md): effective = max(sqrt(max(printed, reading, method)^2 + composition^2 + conversion^2), scatter). The method floor is the robust between-study scatter of the method class in ORCHID (calibrated) or a documented prior; printed values and printed uncertainties are unchanged.
| Value | Unit | Printed | Reading | Method (class, basis) | Composition | Scatter | Conversion | Effective |
|---|---|---|---|---|---|---|---|---|
| -1373.48 | kJ/mol (basis unstated) | 2.61 | 0.005 | 16 (solution_reaction_calorimetry, calibrated) | 16 | |||
| -274.696 | kJ/mol-atom | 0.522 | 0.001 | 3.2 (solution_reaction_calorimetry, calibrated) | 3.2 | |||
| -266.94 | kJ/mol-atom | 0.01 | 3.2 (solution_reaction_calorimetry, calibrated) | 3.2 | ||||
| -273.64 | kJ/mol-atom | 0.01 | 3.9 (model_calculated, calibrated) | 3.9 |
Sources
- E. Povoden-Karadeniz, A. N. Grundy, M. Chen, T. Ivas, L. J. Gauckler, Thermodynamic Assessment of the La-Fe-O System, J. Phase Equilib. Diffus. 30, 351-366 (2009). doi:10.1007/s11669-009-9501-6