c) Show that dVm by working from the total differential of the state function entropy S(T,...
Please explain as much as possible Consider gases described by the following two equations of state: RT RT b) p a) Perfect: p m 2 Vm -b as ) Use Maxwell Equation to derive an expression for for each equation of state т ii) for an isothermal expansion, compare the change in entropy expected for a perfect gas and for a gas obeying the Van der Waals equation of state (Equations a and b) ii Which has the greatest change...
(a) One mole of a monoatomic van der Waals gas obeys the equation of state A3. ) (V-b)=RT (p+ and its internal energy is expressed as U CvT where Cv is the molar isochoric heat capacity of an ideal gas. The gas is initially at pressure p and volume V (i) Explain the physical meaning of the parameters a and b in the equation of state of the gas (ii) Write down the equation that defines entropy in thermodynamics. Define...
(a) Show that the entropy change of a Van der Waals gas for an isothermal change V1 to V2 is: ΔS = nR ln (V2 - nb / V1 - nb) (b) Calculate ΔS for expanding on mole of NH3 from 2 dm3 to 20 dm3. Compare this to the ideal gas result. b = 0.0371 dm3/mol
(30pts) Derive expressions for a gas that obeys the Van der Waals equation of state of (P+a⁄v²)(v-b)=RT where v is specific volume and a and b are constants. For an isothermal process derive expressions to calculate change in enthalpy (h), change in internal energy(u), change in entropy (s),
The equation of state for a van der Waals fluid is ? You will look at the work and energy it takes to compress such a fluid and compare it to an ideal gas. Show that the following identity is true using thermodynamic identity for U and Maxwell’s Relations. Using part (a), show that for a van der Waals fluid, the internal energy for a monatomic Take a van der Waals fluid at 101 kPa, 300 K, and an initial...
Parts iii) and iv) are the ones I need help with please :) (a) One mole of a monoatomic van der Waals gas obeys the equation of state and its internal energy is expressed as U where Cv is the molar apacity of an ideal gas. The gas is initially at pr isochoric heat c essure p and volume V Explain the physical meaning of the parameters a and b in the equation of state of the gas (ii) Write...
One mole of H20( is supercooled to-5.00°C at 1 bar pressure before freezing at that temperature. Calculate ASys, ASum, and ASeotal for this process. Is it spontaneous? CPm (H20, 1)- 75.3 J/mol.K CPm (H20, s)-37.7 J/mol.K AHfusion 6.008 kJ/mol Hint: remember that ASs is computed using q along a reversible path, while ASur is computed using the actual heat transfer during the freezing. For the following equilibrium reaction: Here is an ICE table, starting from no moles of pure 0z...
Use engineering methodology and show units calculations. Water vapor initially at 240 °C, 1.0 MPa expands in a piston-cylinder assembly isothermally and without internal irreversibilities to a final pressure of 0.1 MPa. Evaluate the (a)work done, in kJ/kg, (b) the change of entropy, in kJ/kg - K and (c) the change of internal energy, in kJ/kg. Assume the system can be treated as a Van der Waals model.. [Given: the specific volume of the water vapor can be determined from...
B3. (20%) (Show all your calculation steps.) Water vapor initially at 240 °C, 1.0 MPa expands in a piston-cylinder assembly isothermally and without internal irreversibilities to a final pressure of 0.1 MPa. Evaluate the (a)work done, in kl/kg, (b) the change of entropy,, in kl/kg-K and (c) the change of internal energy, in kl/kg. Assume the system can be treated as a Van der Waals model.. [Given: the specific volume of the water vapor can be determined from the superheated...
1. The Redlich-Kwong equation of state is given by P=_RT___ A _ _ V-RI2,, - 0.0866 - where 4-0.42748RT - B - P (The R-K constants can be calculated from the critical temperature and pressure of the gas.) This EOS was introduced in 1949 and is adequate for calculations of gas phase properties when P, </2 T, a) Derive an expression for the work associated with an isothermal reversible volume change of a R-K gas between two volumes V, and...