Combined and ideal gas laws
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Transcript Combined and ideal gas laws
Combined and
ideal gas laws
Gas Properties
Gases have mass
Gases diffuse
Gases expand to fill containers
Gases exert pressure
Gases are compressible
Pressure & temperature are
dependent
Gas Variables
Volume
(V)
• Units of volume (L)
Amount (n)
• Units of amount (moles)
Temperature (T)
• Units of temperature (K)
Pressure (P)
• Units of pressure (mmHg)
• Units of pressure (KPa)
• Units of pressure (atm)
A Little Review
Boyle’s
law
• pressure & volume
• as P then V
P 1V 1 =
• at constant T, n
Charles’ law:
• Temperature & volume
• As T then V
T
V
=
1
2
• At constant P, n
P 2V 2
T2V 1
A Little Review
Gay-Lussac’s
law:
• Temperature & pressure
• As P then T
P
T
=
1
2
• At constant V, n
P 2T1
Combined gas law
If
we combine all of the relationships
from the 3 laws covered thus far
(Boyle’s, Charles’s, and GayLussac’s) we can develop a
mathematical equation that can
solve for a situation where 3
variables change :
PV=k1 V/T=k2
P/T=k3
Combined gas law
Amount
is held constant
Is used when you have a change in
volume, pressure, or temperature
P 1V 1
T1
=K=
P2V2
T2
Combined gas law
Amount
is held constant
Is used when you have a change in
volume, pressure, or temperature
P 1V 1
T1
=
P2V2
T2
P 1 V 1 T2 = P2 V 2 T1
Example problem
A gas with a volume of 4.0L at STP.
What is its volume at 2.0atm
and at 30°C?
- P1 1atm
- V1 4.0 L
- T1 273K
- P2 2.0 atm
- V2 ?
- T2 30°C + 273
= 303K
Example problem
P 1V 1
T1
=
P2V2
T2
2.22L = V2
Avogadro’s Law
So
far we’ve compared all the
variables except the amount of a
gas (n).
There is a lesser known law called
Avogadro’s Law which relates V & n.
It turns out that they are directly
related to each other.
As # of moles increases then V
increases.
V/n = k
Ideal Gas Law
Which
leads us to the ideal gas law –
So far we have always held at least
1 of the variables constant.
We can set up a much more powerful
eqn, which can be derived by
combining the proportions expressed
by the previous laws.
Ideal Gas Law
If
we combine all of the laws
together including Avogadro’s Law
mentioned earlier we get:
PV
nT
=R
Normally
written as
Where R is the
universal gas
constant
PV = nRT
Ideal Gas Constant (R)
R is a constant that connects the
4 variables
R is dependent on the units of the
variables for P, V, & T
• Temp is always in Kelvin
• Volume is in liters
• Pressure is in either atm or mmHg
or kPa
Ideal Gas Constant
Because of the different pressure
units there are 3 possibilities for
our ideal gas constant
• If pressure is
given in atm
• If pressure is
given in mmHg
R=.0821 L•atm
mol•K
L•mmHg
R=62.4
mol•K
• If pressure is R=8.314 L•kPa
given in kPa
mol•K
Using the Ideal Gas Law
What volume does 9.45g
of C2H2 occupy at STP?
P 1atm
V
n
?
9.45g
26g
L•atm
R .0821
mol•K
T 273K
= .3635 mol
PV = nRT
(1.0atm)(V) =
L•atm
(.3635mol) (.0821 mol•K
)(273K)
(1.0atm)(V)= (8.147L•atm)
V = 8.15L
A camping stove propane tank holds
3000g of C3H8. How large a
container would be needed to hold
the same amount of propane as a gas
at 25°C and a pressure of 303 kpa?
L•kPa
8.31
P 303kPa R
V
n
?
3000g
44g
mol•K
T 298K
= 68.2 mol
PV = nRT
(303kPa)(V)=
(68.2 mol) (8.31
L•kPa
)
mol•K
(298K)
(303kPa) (V) = (168,970.4 L•kPa)
V = 557.7L
Ideal Gas Law & Stoichiometry
What volume of hydrogen gas must
be burned to form 1.00 L of
water vapor at 1.00 atm pressure
and 300°C?
PV = nRT
(1.00 atm)(1.00 L)
nH2O=
(.0821L atm/mol K)(573K)
nH2O= .021257 mols
Ideal Gas Law & Stoichiometry
2H2 + O2 2H2O
.021257 mol
2 mol H2
22.4 L H2
2 mol H2O
1mol H2
.476 L H2
=
Loose Ends of Gases
• There are a couple more laws that
we need to address dealing with
gases.
– Dalton’s Law of Partial Pressures
– Graham’s Law of Diffusion and
Effusion.
Dalton’s Law of Partial Pressure
• States that the total pressure of a
mixture of gases is equal to the sum
of the partial pressures of the
component gases.
PT=P1+P2+P3+…
• What that means is that each gas
involved in a mixture exerts an
independent pressure on its
containers walls
Dalton’s Law of Partial Pressure
• Therefore, to find the pressure in
the system you must have the total
pressure of all of the gases
involved.
• This becomes very important for
people who work at high altitudes
like mountain climbers and pilots.
• For example, at an altitude of about
10,000m air pressure is about 1/3
of an atmosphere.
Dalton’s Law of Partial Pressure
• The partial pressure of oxygen at
this altitude is less than 50 mmHg.
• By comparison, the partial pressure
of oxygen in human alveolar blood
needs to be about 100 mmHg.
• Thus, respiration cannot occur
normally at this altitude, and an
outside source of oxygen is needed
in order to survive.
Simple Dalton’s Law Calculation
• Three of the primary components of
air are CO2, N2, and O2. In a
sample containing a mixture of
these gases at exactly 760 mmHg,
the partial pressures of CO2 and N2
are given as PCO2= 0.285mmHg
and PN2 = 593.525mmHg. What is
the partial pressure of O2?
Simple Dalton’s Law Calculation
PT = PCO2 + PN2 + PO2
760mmHg = .285mmHg +
593.525mmHg + PO2
PO2= 167mmHg
Dalton’s Law of Partial Pressure
• Partial Pressures are also
important when a gas is collected
through water.
— Any time a gas is collected
through water the gas is
“contaminated” with water vapor.
— You can determine the pressure of
the dry gas by subtracting out the
water vapor
Atmospheric
Pressure
Ptot = Patmospheric pressure = Pgas + PH2O
— The water’s vapor pressure can be
determined from a list and subtracted from the atmospheric pressure
WATER VAPOR PRESSURES
Temp (°C)
Vapor pressure (kPa)
1
5
10
15
20
25
30
35
40
45
50
0.65176
.87260
1.2281
1.7056
2.3388
3.1691
4.2455
5.6267
7.3814
9.5898
12.344
WATER VAPOR PRESSURES
Temp (°C)
Vapor pressure (kPa)
55
60
65
70
75
80
85
90
95
100
105
15.752
.19.932
25.022
31.176
38.563
47.373
57.815
70.117
84.529
101.32
120.79
Simple Dalton’s Law Calculation
• Determine the partial pressure of
oxygen collected by water displacement if the water temperature is
20.0°C and the total pressure of the
gases in the collection bottle is
730 mmHg.
PH2O at 20.0°C= 2.3388 kPa
We need to convert to mmHg.
Simple Dalton’s Law Calculation
2.3388 kPa
760 mmHg
101.3 kPa
PH2O = 17.5468 mmHg
PT = PH2O + PO2
730mmHg = 17.5468 + PO2
PO2= 712.5 mmHg
Graham’s Law
• Thomas Graham studied the
effusion and diffusion of gases.
– Diffusion is the mixing of gases
through each other.
– Effusion is the process whereby the
molecules of a gas escape from its
container through a tiny hole
Graham’s Law
• Graham’s Law states that the rates
of effusion and diffusion of gases at
the same temperature and pressure
is dependent on the size of the
molecule.
– The bigger the molecule the slower
it moves the slower it mixes and
escapes.
Graham’s Law
• Kinetic energy can be calculated
with the equation ½ mv2
— m is the mass of the object
— v is the velocity.
• If we work with two different at the
same temperature their energies
would be equal and the equation
can be rewritten as:
½ MAvA2 = ½ MBvB2
• “M” represents molar mass
• “v” represents molecular velocity
• “A” is one gas
• “B” is another gas
• If we want to compare both gases
velocities, to determine which gas
moves faster, we could write a ratio
of their velocities.
— Rearranging things and taking the
square root would give the eqn:
vA
vB
=
MB
MA
• This shows that the velocities of two
different gases are inversely proportional to the square roots of their
molar masses.
— This can be expanded to deal with
rates of diffusion or effusion
Rate of effusion of A
Rate of effusion of B
=
MB
MA
Graham’s Law
• The way you can interpret the
equation is that the number of times
faster A moves than B, is the
square root of the ratio of the molar
mass of B divided by the Molar
mass of A
— So if A is half the size of B than it
effuses or diffuses 1.4 times faster.
Graham’s Law Example Calc.
If equal amounts of helium and argon
are placed in a porous container and
allowed to escape, which gas will
escape faster and how much faster?
Rate of effusion of A
Rate of effusion of B
=
MB
MA
Graham’s Law Example Calc.
Rate of effusion of He
Rate of effusion of Ar
=
40 g
4g
Helium is 3.16 times faster than Argon.