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Heat of Vaporization Lab, Lab Reports of Chemistry

You will be able to know about how to determine the heat of vaporization of methanol

Typology: Lab Reports

2020/2021

Uploaded on 05/12/2021

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Expt HV 1
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 dµA = dµB 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)
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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

– V

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

= RT (4)

and Eq. (2) becomes

dp/dT = ∆H vap

/ ( T V

m

Eq. (4) may be rewritten as

V

m

= RT / p (6)

and substituting Eq. (6) into Eq. (5) gives

dp/dT = ∆H vap

/ ( R T

2

/ p ). (7)

Rearranging Eq. (7) gives

dp/dT = p (∆H vap

/ R T

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

  1. Prepare the Temperature Probe and Pressure Sensor for data collection.

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.

  1. Prepare for data collection for data collection on electronic device. The vertical axis may

have pressure scaled from 90 to 135 kPa. The horizontal axis will need to have temperature

scaled to fit the data range you collect.

  1. The temperature and pressure readings should be displayed in the Meter Window. Record

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.

  1. Set up the apparatus shown in Figure 2. Place about 10mL of methanol into the 125mL

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.

  1. Sometimes data may be lost. To err on the side of caution, as data is collected, you should

also record values by hand in your lab notebook.

  1. Open the side valve of the Pressure Sensor so the Erlenmeyer flask is open to the atmosphere.

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.

  1. When you are finished, use "Shut Down" to turn off the computer, and clean up your work

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.

  1. Celsius temperatures must be converted to Kelvin (K) prior to analysis.
  2. The Clausius-Clapeyron equation describes the relationship between vapor pressure and

temperature:

ln P = – ΔH vap

/ RT + B

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

/ R ) •

T

+ B

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.

  1. Create new columns to generate ln P and 1/T values.
  1. Plot ln P versus 1/T using EXCEL and perform a linear regression least squares fit. Leave

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.

  1. Report slope, intercept, and r

2

values and determine units for the slope, m , of the regression

line.

  1. Use the slope value to calculate the heat of vaporization for methanol

m = - ΔH vap

/ R.

  1. You report will include a data table and plot of ln(P) versus 1/T from which you will

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.