Chemical potential and collegiative properties Flashcards
chemical potential at equilibrium
mu1 = mu2
relationship between mu and G
mu is a molar form of Gibbs energy
General change in pressure with temperature for a phase change
dp/dT = dHtrans/dTtrans
Fusion pressure and temperature changes
p2 - p1 = dH/dV(ln(T2/T1))
Evaporation temperature and pressure changes
ln(p2/p1) = -dH/R(1/T2 - 1/T1)
sublimation temperature and pressure changes
ln(p2/p1) = -dH/R(1/T2 - 1/T1)
What is Gibbs energy of a system the sum of
The sum of the partial molar chemical potentials of each species in the system
How does Gibbs vary with pressure, temperature and composition
dG = Vdp - SdT + sum(mun)
mun = partial molar chemical potential
what is Xr or Xb etc
molar fraction of a species
entropy of mixing
dS = -nR[XrlnXr + XblnXb]
Gibbs of mixing
dG = nRT[XrlnXr + XblnXb]
Chemical potential and its relationship with vapour pressure
The phase change between liquid and gas is in equilibrium and so, the chemical potential of the gas and liquid are equal
Chemical potential of a mixture
mu = mu* + RTln(pa/pa )
mu = mu of the pure species
pa* = pressure of the pure species
Raoult’s law, conditions and assumptions
pa = Xapa*
for concentrated solutions or dilute solutions with similar solvent and solute properties as the solute is assume to behave ideally when surrounded by other solute molecules
* means pure solution
Raoult’s law and chemical potential
Xa = pa/pa* therefore
mu = mu* + RTln(Xa)
Henry’s law, conditions and assumptions
pa = khXa
for dilute solution as the solute is assumed to act ideally when surrounded by solvent molecules
osmotic pressure
the pressure required to prevent osmosis
osmotic pressure equation
O = njRT/Vm
nj = number of moles of solute
Vm = partial molar volume
osmotic pressure of an ideal solution
Vm = molar volume
therefore
O = cRT
c = molar conc of solute in molm-3
osmometer calculation
p = rgh
r = density
g = acceleration due to gravity
h = height in m
Change in the melting or boiling point temperature of a mixture
dT = (RT^2/dH)Xb
T = temperature of pure fusion or vapourisation
dH = enthalpy change of pure fusion or vaporisation
Xb = molar fraction of the original
Units for the change in boiling or freezing temperatures of a mixture
dH is in Jmol-1
T is in kelvin
What makes ice slippery?
A mode predicts that the upper layers of ice are not true solids, but instead partial liquids. This is maintained even at temperatures well below freezing point which allows for ice to be slippery both at these temperatures, and when very little pressure is applied
enthalpy change of mixing
0 kJmol-1
What does it mean practically if mixing is endo or exothermic
If exothermic, the reaction with be spontaneous and energetic. If endothermic, the driving force becomes entropy and if it is not large enough, the species are immiscible
Deviations from Raoult’s law
Positive: if A-B interactions are weak and species prefer to be separated
Negative: is A-B interactions are strong and species prefer to be mixed