Because (∂H/∂P)T =−CPμJ−T, the change in enthalpy of a gas expanded at constant temperature can be calculated. To do so, the functional dependence of μJ−T on P must be known.
Part A Treating Ar as a van der Waals gas, calculate ΔH when 1 mole of Ar is expanded from 329 bar to 1.68 bar at 375 K. Assume that μJ−T is independent of pressure and is given by μJ−T=[(2a/RT)−b]/CP,m, and CP,m=5/2R for Ar. The van der Waals parameters a and b for Ar are 1.355 bar⋅dm6⋅mol−2 and 0.0320 dm3⋅mol−1, respectively.
Part B What value would ΔH have if the gas exhibited ideal gas behavior?
Because (∂H/∂P)T =−CPμJ−T, the change in enthalpy of a gas expanded at constant temperature can be...
l Lie vai der Waals constants. 5. Compare th e pressures given by the perfect gas equation and the van der Waals equation for propane at 400 K and p 10.62 mol dm-3. The van der Waals constants for propane are for a- 9.3919 dm6 bar mol-2 and b0.090494 dm3 mol-1 Given that the vibrational frequency p = 4401 cm' for Ha, calculate the vibrational energe fo 6.
One mole of a gas is expanded from 0.1 bar to 0.01 bar at a constant temperature of 350 K. The gas obeys the equation of state p(Vm - b) = RT where b is a constant equal to 0.01 dm3 mol-1. Find ΔH in mJ for this process.
Van der Waals Constants Gas CH4 CO2 Cl2 NH3 H20 Xe CCIA 02 N2 Kr a b (bar.L2/mol2) (atm-L2/mol)(L/mol) 2.303 2.273 0.0431 3.658 3.610 0.0429 6.343 6.260 0.0542 4.225 4.170 0.0371 5.537 5.465 0.0305 4.192 4.137 0.0516 20.01 19.75 0.1281 1.382 1.363 1.370 1.351 5.121 5.193 1.355 0.0319 0.0387 0.0106 0.0320 0.0395 Ar 1.336 CO 1.472 1.452 4.544 4.481 0.0434 1.370 1.351 0.0387 3.852 3.799 0.0444 5.36 5.29 0.0443 H2S NO N20 NO2 SO2 HF HCI HBr 6.865 6.770 0.0568...
For a Van der Waals gas, the following equations hold. P = nRT/(V−nb) − a(n/V)2 dU = CV dT + a(n/V)2 dV For chlorine gas, CV,m = 25.6 J K−1 mol−1, a = 6.343 bar L2 mol−2, and b = 0.0542 L mol−1. Calculate q, w, ΔU, and ΔH, in joules, when one mole of chlorine gas is expanded isothermally and reversibly at 449 K from 7.0 L to 15.0 L.
Initially, at a temperature T, and a molar volume vi, a van der Waals gas undergoes a change of state to the final temperature T2 and the molar volume V2. The van der Waals gas is characterized by the two parameters a and b (cf. Eq. (3.3)). a. Show that the change in molar entropy is As = c, In 72 + R In º2 = (3.62) 01 - 6 b. A volume of 1 dm is partitioned by a...
Atomic gas which obeys Van der Waals equation of state RT= (P+ a/ V2) (V-b) has internal energy (per mole) of u = 3/2 RT - a/V where 'V' is volume of mole in temperature T. In the beginning, the gas temperature is T1 and volume V1. The gas is let to expand adiabatically so that its final volume is V2. What is the final temperature of the gas?
The van der Waals equation gives a relationship between the pressure p (atm), volume V(L), and temperature T(K) for a real gas: .2 where n is the number of moles, R 0.08206(L atm)(mol K) is the gas con- stant, and a (L- atm/mol-) and b (L/mol) are material constants. Determine the volume of 1.5 mol of nitrogen (a .39 L2 atm/mol2. b = 0.03913 L/mol) at temperature of 350 K and pressure of 70 atm. The van der Waals equation...
< Question 4 of 30 Attempt 2 Use the van der Waals equation of state to calculate the pressure P of 3.50 mol of CH, at 489 K in a 5.20 L vessel. Use this list of van der Waals constants. P= 26.8 atm Use the ideal gas equation to calculate the pressure P under the same conditions. 10:19 PM 7/30/2020 < IUL ub e . 3 Question 4 of 30 > Attempt 2 P= 26.8 atm Use the ideal...
4. The enthalpy H may be written as a function of temperature T and pressure P. If we have a system whose composition remains constant and using Maxwell's equations and the total differential, we can write dH as avdP where Cp is the heat capacity at constant pressure and the subscript of P on the partial derivative represents the partial of volume with respect to temperature holding pressure connstant. Find the change in enthalpy (A) for an ideal gas undergoing...