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Thermodynamics is a branch of physics that deals with heat, work, and temperature, and their relation to energy, entropy, and the physical properties of matter and ...
Thermal physics, generally speaking, is the study of the statistical nature of physical systems from an energetic perspective. Starting with the basics of heat and temperature, thermal physics analyzes the first law of thermodynamics and second law of thermodynamics from the statistical perspective, in terms of the number of microstates corresponding to a given macrostate.
In thermodynamics, the Shimansky equation describes the temperature dependence of the heat of vaporization (also known as the enthalpy of vaporization or the heat of evaporation): [1] = where: L is the latent heat of vaporization at the temperature T,
The behavior of a thermodynamic system is summarized in the laws of Thermodynamics, which concisely are: . Zeroth law of thermodynamics; If A, B, C are thermodynamic systems such that A is in thermal equilibrium with B and B is in thermal equilibrium with C, then A is in thermal equilibrium with C.
For quasi-static and reversible processes, the first law of thermodynamics is: d U = δ Q − δ W {\displaystyle dU=\delta Q-\delta W} where δQ is the heat supplied to the system and δW is the work done by the system.
The history of thermodynamics is fundamentally interwoven with the history of physics and the history of chemistry, and ultimately dates back to theories of heat in antiquity. The laws of thermodynamics are the result of progress made in this field over the nineteenth and early twentieth centuries.
In physics and engineering contexts, especially in the context of diffusion through a medium, it is more common to fix a Cartesian coordinate system and then to consider the specific case of a function u(x, y, z, t) of three spatial variables (x, y, z) and time variable t. One then says that u is a solution of the heat equation if
Entropy is a state function and is defined in an absolute sense through the Third Law of Thermodynamics as S = ∫ 0 T d Q r e v T {\displaystyle S=\int _{0}^{T}{dQ_{rev} \over T}} where a reversible path is chosen from absolute zero to the final state, so that for an isothermal reversible process