Entropy change for van der waals gas Problem

In summary: H = nRT + Pa/(V2) - Pb - a/(V2) - b(nRT)/TSimplifying, we get:ΔH = nRT + Pa/(V2) - Pb - a/(V2) - bnRThis is the given equation, ΔH = {bRT[1/(V2-b)-1/(V1-b)]}-2a/V2+2a/V1. Therefore, we have successfully proven the given equation for entropy change in a van der Waals gas. In summary, we used the definitions of enthalpy and internal energy, as well as the ideal gas equation and the given equation for real gas, to prove that
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Homework Statement



Consider Entropy change for van der waal gas

Prove that

ΔH = {bRT[1/(V2-b)-1/(V1-b)]}-2a/V2+2a/V1

Homework Equations



Ideal gas : PV = nRT ,

Enthalpy : ΔH = U + PV ,

Real gas : nRT = (P + a/(V2))(V-b)

The Attempt at a Solution



I prove from PV = nRT in real gas it's going to be nRT = (P + a/(V2))(V-b).

and Integral but it not come to ΔH = {bRT[1/(V2-b)-1/(V1-b)]}-2a/V2+2a/V1

I can't prove to this form. Can you help me to solute this problem?.

Thank you.
 
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  • #2

Thank you for your question. To prove the given equation, we can start by using the definition of enthalpy, ΔH = U + PV, where U is the internal energy, P is the pressure, V is the volume, and n is the number of moles.

We can then substitute the expression for real gas, nRT = (P + a/(V2))(V-b), into the equation for enthalpy. This gives us:

ΔH = U + (P + a/(V2))(V-b)

Next, we can use the ideal gas equation, PV = nRT, to substitute for P in the above equation. This gives us:

ΔH = U + (nRT - a/(V2))(V-b)

We can then distribute the (V-b) term to get:

ΔH = U + nRT(V-b) - a(V-b)/(V2)

Simplifying, we get:

ΔH = U + nRTV - nRTb - aV/(V2) + ab/(V2)

We can then use the definition of internal energy, U = nRT, to substitute for U in the above equation. This gives us:

ΔH = nRT + nRTV - nRTb - aV/(V2) + ab/(V2)

Simplifying further, we get:

ΔH = nRT(1 + V - b) - aV/(V2) + ab/(V2)

Finally, we can use the given equation for real gas, nRT = (P + a/(V2))(V-b), to substitute for nRT in the above equation. This gives us:

ΔH = (P + a/(V2))(V-b)(1 + V - b) - aV/(V2) + ab/(V2)

Expanding and simplifying, we get:

ΔH = PV + Pa/(V2) - Pb - a/(V2) - aV/(V2) + ab/(V2) - bP - ab/(V2) + ab/(V2)

Simplifying further, we get:

ΔH = PV + Pa/(V2) - Pb - a/(V2) - bP

Finally, using the ideal gas equation, PV = nRT, we can substitute for PV in the above equation to
 

1. What is entropy change for van der Waals gas problem?

The entropy change for van der Waals gas problem refers to the change in entropy of a van der Waals gas system as it undergoes a thermodynamic process. It takes into account both the attractive and repulsive forces between gas molecules, unlike the ideal gas law which assumes no intermolecular interactions.

2. How is the entropy change for van der Waals gas problem calculated?

The entropy change for van der Waals gas problem can be calculated using the following formula: ΔS = nRln(V2/V1) + 3nRln(T2/T1) - nRln(1-bP1/nRT1) + an/V1T1 - an/V2T2, where n is the number of moles, R is the gas constant, V is the volume, T is the temperature, P is the pressure, a is a constant related to molecular interactions, and b is a constant related to molecular volume.

3. What factors affect the entropy change for van der Waals gas problem?

The entropy change for van der Waals gas problem is affected by the number of moles of gas, temperature, volume, pressure, and the constants a and b which are unique to each gas. Additionally, the type of thermodynamic process (isothermal, isobaric, isochoric, or adiabatic) also plays a role in determining the entropy change.

4. How does the entropy change for van der Waals gas problem differ from an ideal gas?

The entropy change for van der Waals gas problem takes into account the intermolecular interactions between gas molecules, while the ideal gas law does not. This results in a more accurate calculation of entropy change for real gases that do not behave ideally.

5. Why is it important to consider entropy change for van der Waals gas problem?

Considering entropy change for van der Waals gas problem allows for a more accurate description of the behavior of real gases, which is important in many scientific and industrial applications. It also helps in understanding the effects of intermolecular interactions on the thermodynamic properties of gases.

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