Trouble with Gibbs free energy equation

In summary, the Gibbs formula dG= VdP-SdT can be applied to any closed system with only reversible processes. In solid and liquid systems, the variation of pressure is equal to the pressure in the gas phase. In a system of liquid and vapor at equilibrium, the pressure within the gas is the same as the pressure within the liquid. However, in a perfect vacuum, the solid will not be at equilibrium and will have a very low equilibrium vapor pressure.
  • #1
Eureka99
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Hi everybody! Lately I tried to overcome some problems with understanding thermodynamics laws, and unfortunately I couldn't find anything about my question:nb) and I really hope someone can help me here...
My question is:
This version of Gibbs formula dG= VdP-SdT, can be applied to any close system, in which occur only reversible processes, if I understood well, and so I was wondering, with solid or liquid systems, what is the variation of Pressure, if there is any? I mean, with gases it might be the variation of the internal pressure of the gas, but with solids and liquids, I saw my book in a example about chemical potentials of vapor and liquid in equilibrium, that as dP of the liquid, it takes the variation of the total pressure ON the liquid. But that seems to me not legit, and only confuses me more.
I apologize for eventual inaccuracies, but I would appreciate it so much, if someone helps me making this clear!
Thank you in advance
 
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  • #2
Eureka99 said:
Hi everybody! Lately I tried to overcome some problems with understanding thermodynamics laws, and unfortunately I couldn't find anything about my question:nb) and I really hope someone can help me here...
My question is:
This version of Gibbs formula dG= VdP-SdT, can be applied to any close system, in which occur only reversible processes, if I understood well, and so I was wondering, with solid or liquid systems, what is the variation of Pressure, if there is any? I mean, with gases it might be the variation of the internal pressure of the gas, but with solids and liquids, I saw my book in a example about chemical potentials of vapor and liquid in equilibrium, that as dP of the liquid, it takes the variation of the total pressure ON the liquid.
How many pressures do you think there are?

Chet
 
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  • #3
Your question actually made me realize how silly my question was, and now I really seem and feel like a stupid...the fact that confused me is that, when I think about the pressure as a definition of any force applied on a surface, I was thinking of a system composed only for example by a liquid in a container, and so I was wondering if the pressure can be considered as the pressure that the liquid applies on the internal surfaces of the container, and so the hydrostatic pressure. Now that I see, it is actually granted that the pressure is referred to a gas (that can be the atmosphere or else), but when I thought about it for a moment, and about the motion of the particles of the system (like vibrating motion in solids and liquids) that can apply a resultant force on the surroundings, I came to a doubt, but clearly I've been confusing many different things that are not related in this case.
So, I thank you for your response.
 
  • #4
Eureka99 said:
Your question actually made me realize how silly my question was, and now I really seem and feel like a stupid...the fact that confused me is that, when I think about the pressure as a definition of any force applied on a surface, I was thinking of a system composed only for example by a liquid in a container, and so I was wondering if the pressure can be considered as the pressure that the liquid applies on the internal surfaces of the container, and so the hydrostatic pressure. Now that I see, it is actually granted that the pressure is referred to a gas (that can be the atmosphere or else), but when I thought about it for a moment, and about the motion of the particles of the system (like vibrating motion in solids and liquids) that can apply a resultant force on the surroundings, I came to a doubt, but clearly I've been confusing many different things that are not related in this case.
So, I thank you for your response.
Pressure is not just something that exists at surfaces. It exists throughout the gas and throughout the liquid. Plus, in the present thermodynamic context, it is assumed that hydrostatic effects are negligible.
In a system of liquid and vapor at equilibrium, the pressure within the gas is the same as the pressure within the liquid.
 
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  • #5
Chestermiller said:
Pressure is not just something that exists at surfaces. It exists throughout the gas and throughout the liquid. Plus, in the present thermodynamic context, it is assumed that hydrostatic effects are negligible.
In a system of liquid and vapor at equilibrium, the pressure within the gas is the same as the pressure within the liquid.

Oh, now I see... but what about solids? I'm sorry for bothering you with trivial questions, but if for example we have a system with a solid in a vacuum, is the solid going to have a pressure, or is it going to be 0 (if there is the possibility that the solid remains in its state) ?
 
  • #6
Eureka99 said:
Oh, now I see... but what about solids? I'm sorry for bothering you with trivial questions, but if for example we have a system with a solid in a vacuum, is the solid going to have a pressure, or is it going to be 0 (if there is the possibility that the solid remains in its state) ?
If the solid is in a perfect vacuum, it is not at equilibrium. At equilibrium, there will be molecules of the solid material in the gas phase. That is, like liquids, solids have vapor pressure also. At equilibrium, the pressure in the solid is equal to the pressure in the vapor phase. The equilibrium vapor pressure is usually very low, however.
 
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  • #7
Chestermiller said:
If the solid is in a perfect vacuum, it is not at equilibrium. At equilibrium, there will be molecules of the solid material in the gas phase. That is, like liquids, solids have vapor pressure also. At equilibrium, the pressure in the solid is equal to the pressure in the vapor phase. The equilibrium vapor pressure is usually very low, however.

And so I can know the pressure within a liquid or a solid, only in case the total system is in equilibrium with the vapor phase ( plus eventually any other gas added to the system)? Last thing is, I need to visualize the concept of pressure because seeing it only as something applied on surfaces is clearly causing me troubles in understanding systems, and so I ask what generates exactly pressure? Is it the resultant force of particles's motion or is related to something else?
I really thank you for your time.
 
  • #8
Eureka99 said:
And so I can know the pressure within a liquid or a solid, only in case the total system is in equilibrium with the vapor phase ( plus eventually any other gas added to the system)?
That's all you could get from Thermodynamics. Thermodynamics focuses mainly on equilibrium states. To analyze what is happening during the transition between equilibrium states, you need to study Transport Phenomena.
Last thing is, I need to visualize the concept of pressure because seeing it only as something applied on surfaces is clearly causing me troubles in understanding systems, and so I ask what generates exactly pressure? Is it the resultant force of particles's motion or is related to something else?
I really thank you for your time.
If you think of a small imaginary cube within a gas (away from any solid surfaces), there are gas molecules carrying momentum through the walls of the cube from outside to inside, and there are gas molecules carrying momentum through the walls of the cube from inside to outside. This is equivalent to what happens at a solid surface where gas molecules bounce off the surface. And, if you replaced one of the walls of your imaginary cube with a thin planar solid surface, you would measure pressure on each side of the surface from the molecules bouncing off its two sides, but nothing else would be any different.

Chet
 
  • #9
Chestermiller said:
That's all you could get from Thermodynamics. Thermodynamics focuses mainly on equilibrium states. To analyze what is happening during the transition between equilibrium states, you need to study Transport Phenomena.

If you think of a small imaginary cube within a gas (away from any solid surfaces), there are gas molecules carrying momentum through the walls of the cube from outside to inside, and there are gas molecules carrying momentum through the walls of the cube from inside to outside. This is equivalent to what happens at a solid surface where gas molecules bounce off the surface. And, if you replaced one of the walls of your imaginary cube with a thin planar solid surface, you would measure pressure on each side of the surface from the molecules bouncing off its two sides, but nothing else would be any different.

Chet

Now, I think I got it... for now I don't think I have anymore questions related, I have to fix some concepts, and I thank you very much for your help it has really helped me. Even if those concepts are very basic, sometimes even if I study more complex things, I realize that I kind of missed them, because I've never stopped before thinking deeply on their meaning (like in this case of pressure). So, I really appreciate your help.
Thank you very much again!
 

Related to Trouble with Gibbs free energy equation

1. What is the Gibbs free energy equation?

The Gibbs free energy equation, also known as the Gibbs-Helmholtz equation, is a thermodynamic equation that relates the change in Gibbs free energy (∆G) of a system to its temperature (T), change in enthalpy (∆H), and change in entropy (∆S). It is commonly used to determine whether a chemical reaction is spontaneous or non-spontaneous.

2. How is the Gibbs free energy equation derived?

The Gibbs free energy equation is derived from the fundamental thermodynamic equations of internal energy, enthalpy, and entropy. It is based on the concept of thermodynamic potentials, where Gibbs free energy is the potential energy of a system that is available to do work at constant temperature and pressure.

3. Can the Gibbs free energy equation be applied to biological systems?

Yes, the Gibbs free energy equation can be applied to biological systems, as it is a fundamental equation of thermodynamics that applies to all types of systems. It is commonly used in biochemistry and biophysics to analyze and predict biochemical reactions and processes.

4. What is the significance of a negative Gibbs free energy value?

A negative value for Gibbs free energy (∆G < 0) indicates that a reaction or process is spontaneous, meaning it can occur without the input of external energy. This is because the system has a lower energy state after the reaction than before, and therefore the reaction will naturally occur.

5. How is the Gibbs free energy equation related to equilibrium?

The Gibbs free energy equation is related to equilibrium through the concept of Gibbs free energy change (∆G). At equilibrium, ∆G = 0, meaning that the system is in a state of minimum free energy and no further spontaneous change will occur. By calculating the ∆G value, we can determine the direction in which a reaction or process will proceed to reach equilibrium.

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