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You will be able to know about how to determine the heat of vaporization of methanol
Typology: Lab Reports
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Heat of Vaporization (HV)
Objective
The purpose of this experiment is to determine the heat of vaporization of methanol.
Background
In this experiment, you will investigate the relationship between the vapor pressure of a
liquid and its temperature. When a liquid is added to an Erlenmeyer flask, it will evaporate into
the air above it in the flask. Eventually, equilibrium is reached between the rate of evaporation
and the rate of condensation. At this point, the vapor pressure of the liquid is equal to the partial
pressure of its vapor in the flask. Pressure and temperature data will be collected using a Pressure
Sensor and a Temperature Probe. Liquid will be placed in a flask and heated to boiling in a water
bath (water will not be boiling) to allow the vapor to fill the flask and displace any air. The flask
will be sealed and the temperature varied. As the water bath temperature is varied, the
temperature of the liquid is varied and the effect of temperature on vapor pressure is observed.
Pairs of temperature and pressure data are collected.
Caution
Methanol is flammable and poisonous.
Theory
As shown in your Physical Chemistry textbook, it is possible by setting the change in
chemical potential of two phases equal to each other dμ A
= dμ B
to derive the equation
dp/dT = ∆S/∆V (1)
where dp is the change in pressure and dT is the change in temperature along a phase diagram
line separating two phases (A and B). ∆S is the entropy difference and ∆V is the volume
difference between one mole of two phases. Eq. (1) can be modified since ∆S = ∆H/T to give
dp/dT = ∆H / ( T ∆V) (2)
where ∆H is the molar enthalpy change associated with a phase change between the two phases.
Either Eq. (1) or (2) above may be referred to as the Clapeyron Equation.
In the special case of liquid and vapor equilibrium, ∆H is ∆H vap the heat of vaporization and
T is the boiling point which depends on the external pressure. ∆V m , the change in volume per
one mole of gas, is given by V m
m,liq where V m is the volume of one mole of the gas (molar
volume) and V m,liq is the volume of one mole of the liquid. To a very good approximation ∆V m
may be given by V m
since the gas volume is so much greater than the volume of an equivalent
amount of liquid. Therefore, since for a mole a gas n = 1 then
p V = n R T (3)
becomes
p V m
and Eq. (2) becomes
dp/dT = ∆H vap
m
Eq. (4) may be rewritten as
m
= RT / p (6)
and substituting Eq. (6) into Eq. (5) gives
dp/dT = ∆H vap
2
/ p ). (7)
Rearranging Eq. (7) gives
dp/dT = p (∆H vap
2
or
in the above calculation if you used the R value 0.08206 (L atm/ mol K), the units would not
work and this would tell you that you had made a mistake in your choice of R.
We are ignoring some more detailed aspects of the theory and analysis by assuming that we
are dealing with an ideal gas and that ∆Hvap is constant over a range of temperature. For a real
gas
pV m = z R T (13)
where z is the compressibility. For extremely low pressures, z is close to 1 and you have ideal
gas behavior. For moderate pressures, z is slightly less than 1. As temperature is increased. both
z and ∆H vap
tend to decrease so the ratio of these tends to remain constant. To simplify your
calculations, we are assuming z =1 (methanol vapor is acting like an ideal gas) and ∆H vap
is
invariant with temperature. These assumptions are one source of error in your experiment.
Procedure
a. The Pressure Sensor should to Channel 1 of the interface device.
b. The Temperature Probe should be connected to Channel 2.
c. Locate the rubber-stopper assembly and the piece of heavy-wall plastic tubing connected
to one of its two valves. Attach the connector at the free end of the
plastic tubing to the open stem of the Pressure Sensor with a
clockwise turn. Leave its two-way valve on the rubber stopper
open (lined up with the valve stem as shown in Figure 1) until
later.
have pressure scaled from 90 to 135 kPa. The horizontal axis will need to have temperature
scaled to fit the data range you collect.
the value for atmospheric pressure in your lab notebook (round to the nearest 0.1 kPa).
Record the barometric pressure using the mercury manometer or pressure gauge on the wall
22
Figure 1
(ask your instructor for directions to use) and convert to kPa. Is your electronic reading
close? Record the room temperature on the wall thermometer and compare to your electronic
reading. Are the two temperatures close? Make sure the pressure and temperature are
reasonable values for the room before continuing.
Erlenmeyer flask. Add about 10 to 15 boiling chips to flask. Place the large liter beaker on
the heater/stirrer. Place stir bar in beaker and partially fill with water. Clamp flask as low as
it can go into beaker and place and clamp temperature probe into water next to flask. Fill
with water to top of beaker. The mouth of the flask will be above the water. Set stir on
maximum or close to maximum.
Heater/Stirrer
Methanol with boiling chips
Water
Temperature Sensor
Pressure Sensor
Figure 2
Stir bar
range. When the flask is sealed with stopper, you do not want to let the pressure go above
about 140kPa or below 55kPa. Since the flask is sealed, we do not want to go to a pressure
too high or too low that might cause the flask to break.
also record values by hand in your lab notebook.
Remove the stopper assembly from the flask and dispose of the methanol into PCHEM
hazardous waste bottle in the hood. Boiling chips should be discarded in paper towel in trash.
area.
Calculations
In your EXCEL spreadsheet create columns with p(kPa), T(
o
C), T(K), ln p, 1/T values and a plot
with linear regression.
temperature:
ln P = – ΔH vap
where ln P i s the natural logarithm of the vapor pressure, Δ H vap
is the heat of vaporization,
T is the absolute temperature, and B is a positive constant. If this equation is rearranged in
slope-intercept form (y = mx + b):
ln P = (– ΔH vap
the slope, m , should be equal to - ΔH vap
/ R. If a plot of ln P vs. 1/T is made, the heat of
vaporization can be determined from the slope of the curve.
out highest temperature value (first data point collected) so that the temperature range is not
too broad. The heat of vaporization is a function of temperature so it is best to not consider
too broad a temperature range.
2
values and determine units for the slope, m , of the regression
line.
m = - ΔH vap
calculate the heat of vaporization. Show calculation of heat of vaporization from slope. Note
that in your analysis you are assuming the solvent vapor follows ideal gas law behavior so
that z=1. Compare your ∆H vap
to that of the literature value of ∆H vap
of methanol at its
normal (1 atm) boiling point.