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An isothermal process is a type of thermodynamic process in which the temperature T of a system remains constant: ΔT = 0. This typically occurs when a system is in contact with an outside thermal reservoir, and a change in the system occurs slowly enough to allow the system to be continuously adjusted to the temperature of the reservoir through heat exchange (see quasi-equilibrium).
The entropy of a given mass does not change during a process that is internally reversible and adiabatic. A process during which the entropy remains constant is called an isentropic process, written Δ s = 0 {\displaystyle \Delta s=0} or s 1 = s 2 {\displaystyle s_{1}=s_{2}} . [ 12 ]
This type of expansion is named after James Prescott Joule who used this expansion, in 1845, in his study for the mechanical equivalent of heat, but this expansion was known long before Joule e.g. by John Leslie, in the beginning of the 19th century, and studied by Joseph Louis Gay-Lussac in 1807 with similar results as obtained by Joule.
In addition, the total change of entropy in both thermal reservoirs over Carnot cycle is zero too, since the inversion of a heat transfer direction means a sign inversion for the heat transferred during isothermal stages: =, +, = Here we denote the entropy change for a thermal reservoir by , = /, where is either for a hot reservoir or for a ...
In thermodynamics, a temperature–entropy (T–s) diagram is a thermodynamic diagram used to visualize changes to temperature (T ) and specific entropy (s) during a thermodynamic process or cycle as the graph of a curve. It is a useful and common tool, particularly because it helps to visualize the heat transfer during a process.
Mathematically, the absolute entropy of any system at zero temperature is the natural log of the number of ground states times the Boltzmann constant k B = 1.38 × 10 −23 J K −1. The entropy of a perfect crystal lattice as defined by Nernst's theorem is zero provided that its ground state is unique, because ln(1) = 0.
Reversible isothermal expansion of the gas at the "hot" temperature, T H (isothermal heat addition or absorption). During this step (A to B) the gas is allowed to expand and it does work on the surroundings. The temperature of the gas (the system) does not change during the process, and thus the expansion is isothermic.
Since the total change in entropy must always be larger or equal to zero, we obtain the inequality W ≤ − Δ F . {\displaystyle W\leq -\Delta F.} We see that the total amount of work that can be extracted in an isothermal process is limited by the free-energy decrease, and that increasing the free energy in a reversible process requires work ...