First order phase transition/constancy of Gibbs

In summary, the conversation discusses the relationship between total entropy and the minimum value of G for a system in equilibrium with a fixed pressure and temperature reservoir. It also explains why at a certain temperature, the value of G is the same for two states with different volumes and discusses the positive nature of latent heat and its expected effect on the change in temperature with pressure. The Clausius-Clapyeron Equation is mentioned as a relevant formula.
  • #1
CAF123
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Homework Statement


a) Starting from the statement that total entropy (Ssystem+Ssurr) can only increase, show that G = U - TS +pV will attain its minimum value for a system in equilibrium with a fixed pressure and temperature reservoir.

b)At atmospheric pressure, a particular substance is found to undergo a discontinuous change between two states at temperature TC when heated. Its volume increases by ΔV and it absorbs latent heat L as its temperature is changed from just below TC to just above TC. Explain why at TC, the value of G is the same for the two states with different volumes.

c)Explain why L must be positive and comment on whether TC is expected to increase or decrease with pressure.

Homework Equations


Clausius-Clapyeron Equation

The Attempt at a Solution


a)Taking the differential of the given equation, I get dG = dU - TdS -SdT +pdV + Vdp. Eliminate two terms because the system is in thermal equilibrium at constant pressure/temperature. This gives dG = dU - TdS + pdV = 0 using the first law. Hence G is mimimum when the boundary conditions of the system permit a constant pressure/temperature environment. I did not really use the fact that the total S ≥ 0 though, so is there another derivation?

b)So is this process occurring at constant pressure and is TC the value of T on the boundary line between the two phases at that particular pressure? If the case, then at TC the two phases instantaneously have the same pressure/temperature. dG = Vdp - SdT = 0, so G is constant over the boundary line.

c) V increases upon heating at constant pressure. So I would imagine this would correspond to an increase in entropy of the system. So l = T(S2-S1) > 0. dP/dT is usually +ve for most substances. So dT/dP is decreasing, so in most cases expect TC to decrease with pressure. Did I do this right?

Many thanks.
 
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  • #2
Also, I thought a latent heat was associated with a change of phase transition at constant temperature. It says that the substance absorbs latent heat from just below Tc to just above Tc, so it is therefore changing temperature, albeit infinitesimally if that is what 'just above (below)' means.
 

Related to First order phase transition/constancy of Gibbs

1. What is a first order phase transition?

A first order phase transition is a type of phase transition in which there is a discontinuous change in the thermodynamic properties of a substance, such as its density, heat capacity, or magnetic susceptibility. This transition occurs at a specific temperature and pressure, known as the critical point.

2. How is a first order phase transition different from a second order phase transition?

In a first order phase transition, there is a discontinuous change in thermodynamic properties, while in a second order phase transition, these properties change continuously. Additionally, a first order phase transition involves a change in the structure of the substance, while a second order phase transition does not.

3. What is the constancy of Gibbs in relation to first order phase transitions?

The constancy of Gibbs refers to the fact that at the critical point of a first order phase transition, the Gibbs free energy, which is a measure of a system's ability to do work, remains constant. This means that at the critical point, the substance can exist in both phases simultaneously without any change in Gibbs free energy.

4. How is the constancy of Gibbs related to the coexistence of phases in a first order phase transition?

The constancy of Gibbs is related to the coexistence of phases in a first order phase transition because it allows for the coexistence of two different phases at equilibrium. This means that at the critical point, the substance can exist in both phases simultaneously without any change in Gibbs free energy, allowing for a smooth transition between the two phases.

5. What is the practical significance of studying first order phase transitions and the constancy of Gibbs?

Understanding first order phase transitions and the constancy of Gibbs is important in fields such as materials science, chemistry, and physics, as it allows for the prediction and control of phase transitions in various substances. This knowledge can also be applied in industries such as pharmaceuticals, where the stability of different phases of a drug can affect its efficacy and shelf-life.

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