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One exception is phosphorus, for which the most stable form at 1 bar is black phosphorus, but white phosphorus is chosen as the standard reference state for zero enthalpy of formation. [2] For example, the standard enthalpy of formation of carbon dioxide is the enthalpy of the following reaction under the above conditions:
The isobaric change in enthalpy H above the common reference temperature of 298.15 K (25 °C) is called the high temperature heat content, the sensible heat, or the relative high-temperature enthalpy, and called henceforth the heat content.
The definition of the Gibbs function is = + where H is the enthalpy defined by: = +. Taking differentials of each definition to find dH and dG, then using the fundamental thermodynamic relation (always true for reversible or irreversible processes): = where S is the entropy, V is volume, (minus sign due to reversibility, in which dU = 0: work other than pressure-volume may be done and is equal ...
Standard enthalpy of formation is the enthalpy change when one mole of any compound is formed from its constituent elements in their standard states. The enthalpy of formation of one mole of ethane gas refers to the reaction 2 C (graphite) + 3 H 2 (g) → C 2 H 6 (g).
The standard Gibbs free energy of formation (G f °) of a compound is the change of Gibbs free energy that accompanies the formation of 1 mole of a substance in its standard state from its constituent elements in their standard states (the most stable form of the element at 1 bar of pressure and the specified temperature, usually 298.15 K or 25 °C).
The technique was developed by professor Sidney William Benson [1] of the University of Southern California. It is further described in Heat of formation group additivity. Heats of formations are intimately related to bond-dissociation energies and thus are important in understanding chemical structure and reactivity. [2]
Low heat values are calculated from high heat value test data. They may also be calculated as the difference between the heat of formation ΔH ⦵ f of the products and reactants (though this approach is somewhat artificial since most heats of formation are typically calculated from measured heats of combustion).. [1]
Std enthalpy change of formation, Δ f H o solid: −1093.99 kJ/mol Standard molar entropy, S o solid: 88.7 J/(mol K) Heat capacity, c p? J/(mol K) Liquid properties Std enthalpy change of formation, Δ f H o liquid? kJ/mol Standard molar entropy, S o liquid? J/(mol K) Heat capacity, c p? J/(mol K) Gas properties Std enthalpy change of ...