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  2. Enthalpy of mixing - Wikipedia

    en.wikipedia.org/wiki/Enthalpy_of_mixing

    Enthalpy of mixing can often be ignored in calculations for mixtures where other heat terms exist, or in cases where the mixture is ideal. [2] The sign convention is the same as for enthalpy of reaction: when the enthalpy of mixing is positive, mixing is endothermic, while negative enthalpy of mixing signifies exothermic mixing. In ideal ...

  3. Standard enthalpy of reaction - Wikipedia

    en.wikipedia.org/wiki/Standard_enthalpy_of_reaction

    The standard enthalpy of reaction (denoted ) for a chemical reaction is the difference between total product and total reactant molar enthalpies, calculated for substances in their standard states. The value can be approximately interpreted in terms of the total of the chemical bond energies for bonds broken and bonds formed.

  4. Standard enthalpy of formation - Wikipedia

    en.wikipedia.org/wiki/Standard_enthalpy_of_formation

    For many substances, the formation reaction may be considered as the sum of a number of simpler reactions, either real or fictitious. The enthalpy of reaction can then be analyzed by applying Hess' law, which states that the sum of the enthalpy changes for a number of individual reaction steps equals the enthalpy change of the overall reaction.

  5. Thermodynamic databases for pure substances - Wikipedia

    en.wikipedia.org/wiki/Thermodynamic_databases...

    C p is therefore the slope of a plot of temperature vs. isobaric heat content (or the derivative of a temperature/heat content equation). The SI units for heat capacity are J/(mol·K). Molar heat content of four substances in their designated states above 298.15 K and at 1 atm pressure. CaO(c) and Rh(c) are in their normal standard state of ...

  6. Extent of reaction - Wikipedia

    en.wikipedia.org/wiki/Extent_of_reaction

    This formula leads to the Nernst equation when applied to the oxidation-reduction reaction which generates the voltage of a voltaic cell. Analogously, the relation between the change in reaction enthalpy and enthalpy can be defined. For example, [8]

  7. Heat of dilution - Wikipedia

    en.wikipedia.org/wiki/Heat_of_dilution

    The heat of dilution can be defined from two perspectives: the differential heat and the integral heat. The differential heat of dilution is viewed on a micro scale, which is associated with the process in which a small amount of solvent is added to a large quantity of solution. The molar differential heat of dilution is thus defined as the enthalpy

  8. Heat of combustion - Wikipedia

    en.wikipedia.org/wiki/Heat_of_combustion

    Since the heat of combustion of these elements is known, the heating value can be calculated using Dulong's Formula: HHV [kJ/g]= 33.87m C + 122.3(m H - m O ÷ 8) + 9.4m S where m C , m H , m O , m N , and m S are the contents of carbon, hydrogen, oxygen, nitrogen, and sulfur on any (wet, dry or ash free) basis, respectively.

  9. Gibbs free energy - Wikipedia

    en.wikipedia.org/wiki/Gibbs_free_energy

    The reaction C (s) diamond → C (s) graphite has a negative change in Gibbs free energy and is therefore thermodynamically favorable at 25 °C and 1 atm. However, the reaction is too slow to be observed, because of its very high activation energy. Whether a reaction is thermodynamically favorable does not determine its rate.