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Philip Koeck
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Does anybody know of a derivation of the van der Waals equation from the molecular kinetic theory of gases, but without using the tools of statistical physics (such as partition functions)?
The van der Waals equation is derived from kinetic theory by considering the behavior of gas particles at the microscopic level. It takes into account the volume of the gas particles and the attractive and repulsive forces between them, which are not accounted for in the ideal gas law.
The derivation of the van der Waals equation assumes that gas particles are point masses with no volume, and that they only interact through elastic collisions. It also assumes that the attractive and repulsive forces between particles are constant and do not change with temperature or pressure.
The van der Waals equation improves upon the ideal gas law by accounting for the volume of gas particles and the intermolecular forces between them. This allows for a more accurate prediction of gas behavior at high pressures and low temperatures, where the ideal gas law breaks down.
No, the van der Waals equation is most accurate for gases that have small molecules and weak intermolecular forces, such as noble gases. It is less accurate for gases with larger molecules and stronger intermolecular forces, such as water vapor or ammonia.
The van der Waals equation is used in various practical applications, such as predicting the behavior of real gases in industrial processes, designing gas storage tanks, and understanding the properties of gases at high pressures and low temperatures. It is also used in the study of phase transitions, such as the liquid-vapor transition.