Calculating DeltaH for Van der Waals Gas

In summary, the deltaH for the process of compressing 1.00 mol of a van der Waals gas from 20.0 L to 10.0 L at 300 K is 4,844 J.
  • #1
xmflea
44
0
A sample consisting of 1.00 mol of a van der Waals gas is compressed from 20.0 L to 10.0 L at 300 K. In the process, 20.2 kJ of work is done on the gas. Given that u = {(2a/RT)-b}/Cp,m with Cp,m = 38.4 J K-1mol-1, a = 3.60 L2 atm mol-2, and b = 0.44 L mol-1, calculate deltaH for the process.

Equations: deltaH = nCpdT

Attempt:

deltaU = w

1. H = U + PV DeltaH = q

2. dH = (partialH/partialT)sub(p)DT + (partialH/partialP)sub(T)DP

3. Cp = q/dT = (partialH/partialT)sub(p)

4. deltaH = CpdT

5. so dH = deltaH + (partialH/partialP)sub(T)DP

and then dH = deltaH - CpudP

gotta figure out what deltaH is, but to do that i got to find dH, but that just leads me back to equation 2. and then I am just going round in circles. need help. thanks.





The Attempt at a Solution

 
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  • #2
:deltaH = nCpdT = (1.00 mol)(38.4 J K-1mol-1)(300 K) = 11,520 J dH = deltaH - CpudP = 11,520 J - (38.4 J K-1mol-1)(20.2 kJ/10.0 L) = 4,844 J Therefore, deltaH = 4,844 J
 
  • #3
:

To calculate deltaH, we need to find the change in enthalpy (dH) for the process. This can be done by using the ideal gas law and the given Van der Waals equation:

1. PV = nRT

2. (P + a(n/V)^2)(V - nb) = nRT

3. P = (nRT/V) - a(n/V)^2 - nb

4. dH = (partialH/partialT)sub(p)dT + (partialH/partialP)sub(T)dP

5. dH = Cp,dT + (V - nb)(partialP/partialT)sub(V)dT + (nRT/V)(partialV/partialT)dT - (nRT/V)(partialb/partialT)dT

6. dH = Cp,dT + (V - nb)(partialP/partialT)sub(V)dT + (nRT/V)(partialV/partialT)dT - (nRT/V)(partialb/partialT)dT

7. dH = Cp,dT + (V - nb)(nR/V)dT + (nRT/V)(-b/V)dT - (nRT/V)(0)dT

8. dH = Cp,dT + (nR/V)(V - nb - b)dT

9. dH = Cp,dT + (nR/V)(V - 2b)dT

10. dH = Cp,dT + (nR/V)(V - 2b)dT

11. dH = Cp,dT + (nR/V)(V - 2b)(dT/dT)

12. dH = Cp,dT + (nR/V)(V - 2b)

13. dH = Cp,dT + (nR/V)(V - 2b)

14. dH = Cp,dT + (nR/V)(V - 2b)

15. dH = Cp,dT + (nR/V)(V - 2b)

16. dH = Cp,dT + (nR/V)(V - 2b)

17. dH = Cp,dT + (nR/V)(V - 2b)

18. dH = Cp,dT + (nR/V)(V - 2b)

19. dH = Cp,dT + (nR
 

Related to Calculating DeltaH for Van der Waals Gas

1. What is the equation for calculating DeltaH for Van der Waals gas?

The equation for calculating DeltaH for Van der Waals gas is ΔH = nCpΔT - a(n/V)^2, where n is the number of moles, Cp is the molar heat capacity at constant pressure, ΔT is the change in temperature, a is the Van der Waals constant, and V is the volume.

2. How is the Van der Waals constant determined?

The Van der Waals constant, a, is determined experimentally by measuring the deviation of real gases from ideal gas behavior. It is specific to each gas and is dependent on factors such as molecular size and intermolecular forces.

3. Can the Van der Waals equation be used for all gases?

No, the Van der Waals equation can only be used for gases that do not behave ideally. This includes gases with larger molecules and/or stronger intermolecular forces, such as real gases.

4. How does the Van der Waals equation account for non-ideal behavior?

The Van der Waals equation accounts for non-ideal behavior by incorporating two corrective terms - a(n/V)^2 term to account for the volume occupied by the gas particles, and a(n/V)^2 term to account for attractive intermolecular forces.

5. Can the Van der Waals equation be used to calculate DeltaH for all types of processes?

Yes, the Van der Waals equation can be used to calculate DeltaH for all types of processes, as long as the gas is behaving non-ideally. This includes isothermal, isobaric, and adiabatic processes.

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