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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. [22] 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.
The concept of thermodynamic entropy arises from the second law of thermodynamics.This law of entropy increase quantifies the reduction in the capacity of an isolated compound thermodynamic system to do thermodynamic work on its surroundings, or indicates whether a thermodynamic process may occur.
Figure 1. A thermodynamic model system. Differences in pressure, density, and temperature of a thermodynamic system tend to equalize over time. For example, in a room containing a glass of melting ice, the difference in temperature between the warm room and the cold glass of ice and water is equalized by energy flowing as heat from the room to the cooler ice and water mixture.
The relationship between entropy, order, and disorder in the Boltzmann equation is so clear among physicists that according to the views of thermodynamic ecologists Sven Jorgensen and Yuri Svirezhev, "it is obvious that entropy is a measure of order or, most likely, disorder in the system."
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.
The Van 't Hoff equation has been widely utilized to explore the changes in state functions in a thermodynamic system. The Van 't Hoff plot, which is derived from this equation, is especially effective in estimating the change in enthalpy and entropy of a chemical reaction.
Boltzmann's equation—carved on his gravestone. [1]In statistical mechanics, Boltzmann's equation (also known as the Boltzmann–Planck equation) is a probability equation relating the entropy, also written as , of an ideal gas to the multiplicity (commonly denoted as or ), the number of real microstates corresponding to the gas's macrostate:
Here S is the entropy of the system; T k is the temperature at which the heat enters the system at heat flow rate ˙; ˙ = ˙ = ˙ represents the entropy flow into the system at position k, due to matter flowing into the system (˙, ˙ are the molar flow rate and mass flow rate and S mk and s k are the molar entropy (i.e. entropy per unit ...