Thermodynamics, Exact differentials

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SUMMARY

This discussion clarifies the distinction between exact differentials and inexact differentials in thermodynamics, specifically regarding pressure (P), volume (V), temperature (T), and internal energy (U). It establishes that work (W) and heat (Q) do not possess exact differentials because they represent processes rather than state functions. The discussion provides a mathematical framework for understanding these concepts, including the use of partial derivatives to determine the existence of a state function. The transformation of the inexact differential dW into an exact differential dU is illustrated through the inclusion of entropy (S) and chemical potential (μ) as additional terms.

PREREQUISITES
  • Understanding of thermodynamic concepts such as state functions and processes
  • Familiarity with partial derivatives and their properties
  • Knowledge of monoatomic gas behavior and relevant variables (V, T, N)
  • Basic grasp of differential calculus in the context of multi-variable functions
NEXT STEPS
  • Study the implications of exact and inexact differentials in thermodynamic processes
  • Learn about the mathematical formulation of state functions in thermodynamics
  • Explore the role of entropy (S) and chemical potential (μ) in thermodynamic systems
  • Investigate applications of partial derivatives in thermodynamic equations
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Students and professionals in physics and engineering, particularly those focusing on thermodynamics, as well as researchers interested in the mathematical foundations of energy transfer processes.

manimaran1605
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There exist exact differential for P (Pressure) ,V (volume) ,T (temperature), U (Internal Energy) but not for W(work), Q (heat) . Why?
 
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That refers to "differential" as in "total differential of multi-variable function". Work and heat are said to not have such total differential because neither work nor heat are usually considered to be such functions. That is because they do not describe one state of a physical system (like internal energy, which is multi-variable function - of volume and temperature, for example), but a whole process such system may undergo.
 
Here's a long-winded description of the difference between exact differentials and inexact differentials:

A generalized differential can be written in the form:

\sum_j Q_j dx_j

where the x_j are independent state variables, and Q_j = Q_j(x_1, x_2, ...) are functions of those state variables. In contrast, an exact differential is the special case where there is a single state function F(x_1, x_2, ...) and

Q_j = \dfrac{\partial F}{\partial x_j}

In that special case, \sum_j Q_j dx_j = dF, an exact differential.

How do you know whether there is such an F? Well, you can figure it out by using a special property of partial derivatives, which is that the order of differentiation doesn't matter:

\dfrac{\partial}{\partial x} \dfrac{\partial}{\partial y} F = \dfrac{\partial}{\partial y} \dfrac{\partial}{\partial x} F

In terms of the Q_j, this means that:

\dfrac{\partial Q_j}{\partial x_k} = \dfrac{\partial Q_k}{\partial x_j}

Now, relating all this back to the question about work:

dW = -P dV

A complete set of independent state variables for a monoatomic gas is volume, temperature and number of particles: V, T, N. So to make an exact differential out of -P dV, you would have to add other terms, to get something like:

d ? = -P dV + Q_1 dT + Q_2 dN

where the mixed derivatives work out:

  • \dfrac{\partial Q_1}{\partial V} = - \dfrac{\partial P}{\partial T}
  • \dfrac{\partial Q_2}{\partial V} = -\dfrac{\partial P}{\partial N}
  • \dfrac{\partial Q_1}{\partial N} = \dfrac{\partial Q_2}{\partial T}

One set of choices that work out are:

Q_1 = S (entropy)
Q_2 = \mu (chemical potential)

With these choices, our inexact differential dW is turned into the exact differential, dU = =Pdv + S dT + \mu dN
 

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