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Changes in entropy are associated with phase transitions and chemical reactions. Chemical equations make use of the standard molar entropy of reactants and products to find the standard entropy of reaction: [3] = The standard entropy of reaction helps determine whether the reaction will take place spontaneously.
Absolute entropy of strontium. The solid line refers to the entropy of strontium in its normal standard state at 1 atm pressure. The dashed line refers to the entropy of strontium vapor in a non-physical state. The standard entropy change for the formation of a compound from the elements, or for any standard reaction is designated ΔS° form or ...
The standard state of a material (pure substance, mixture or solution) is a reference point used to calculate its properties under different conditions.A degree sign (°) or a superscript Plimsoll symbol (⦵) is used to designate a thermodynamic quantity in the standard state, such as change in enthalpy (ΔH°), change in entropy (ΔS°), or change in Gibbs free energy (ΔG°).
The Sackur–Tetrode equation is an expression for the entropy of a monatomic ideal gas. [ 1 ] It is named for Hugo Martin Tetrode [ 2 ] (1895–1931) and Otto Sackur [ 3 ] (1880–1914), who developed it independently as a solution of Boltzmann's gas statistics and entropy equations, at about the same time in 1912.
Standard molar entropy, S o solid? J/(mol K) Heat capacity, c p: 0.212 J/(mol K) at −200°C Liquid properties Std enthalpy change of formation, Δ f H o liquid: −318.2 kJ/mol Standard molar entropy, S o liquid: 180 J/(mol K) Heat capacity, c p: 2.68 J/(gK) at 20°C-25°C Gas properties Std enthalpy change of formation, Δ f H o gas: −261. ...
Uses Antoine's equation: = + from Lange's Handbook of Chemistry 10th ed. Here is a similar formula from the 67th edition of the CRC handbook. Note that the form of this formula as given is a fit to the Clausius–Clapeyron equation, which is a good theoretical starting point for calculating saturation vapor pressures:
Flory–Huggins solution theory is a lattice model of the thermodynamics of polymer solutions which takes account of the great dissimilarity in molecular sizes in adapting the usual expression for the entropy of mixing. The result is an equation for the Gibbs free energy change for mixing a polymer with a solvent. Although it makes simplifying ...
The pure component's molar volume and molar enthalpy are equal to the corresponding partial molar quantities because there is no volume or internal energy change on mixing for an ideal solution. The molar volume of a mixture can be found from the sum of the excess volumes of the components of a mixture: