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Isotherms of an ideal gas for different temperatures. The curved lines are rectangular hyperbolae of the form y = a/x. They represent the relationship between pressure (on the vertical axis) and volume (on the horizontal axis) for an ideal gas at different temperatures: lines that are farther away from the origin (that is, lines that are nearer to the top right-hand corner of the diagram ...
Since an entropy is a state function, the entropy change of the system for an irreversible path is the same as for a reversible path between the same two states. [23] However, the heat transferred to or from the surroundings is different as well as its entropy change. We can calculate the change of entropy only by integrating the above formula.
In the case of an ideal gas, the heat capacity is constant and the ideal gas law PV = nRT gives that α V V = V/T = nR/p, with n the number of moles and R the molar ideal-gas constant. So, the molar entropy of an ideal gas is given by (,) = (,) + . In this expression C P now is the molar heat capacity. The entropy of inhomogeneous ...
The properties of molar internal energy and entropy —defined by the first and second laws of thermodynamics, hence all thermodynamic properties of a simple compressible substance—can be specified, up to a constant of integration, by two measurable functions: a mechanical equation of state = (,) , and a constant volume specific heat
The entropy of the surrounding room decreases less than the entropy of the ice and water increases: the room temperature of 298 K is larger than 273 K and therefore the ratio, (entropy change), of δQ / 298 K for the surroundings is smaller than the ratio (entropy change), of δQ / 273 K for the ice and water system. This is ...
The Van 't Hoff equation relates the change in the equilibrium constant, K eq, of a chemical reaction to the change in temperature, T, given the standard enthalpy change, Δ r H ⊖, for the process. The subscript r {\displaystyle r} means "reaction" and the superscript ⊖ {\displaystyle \ominus } means "standard".
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.
Ludwig Boltzmann defined entropy as a measure of the number of possible microscopic states (microstates) of a system in thermodynamic equilibrium, consistent with its macroscopic thermodynamic properties, which constitute the macrostate of the system. A useful illustration is the example of a sample of gas contained in a container.