cm1502 chapter 7thermodynamics part 1- ideal gas
TRANSCRIPT
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CM 1502 1
Properties of Gases and
Ideal Gas Law
1. States of Matter
2. Ideal Gas Law
3. Four Laws for Ideal Gases
4. Daltons Law of Partial Pressures and Mole Fraction
5. Real Gases
6. Virial (force) and Van der Waals Equations of State for
Real Gases
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CM 1502 2
Physical States of Matter
solid, liquid and gas.
http://www.grc.nasa.gov/WWW/K-12/airplane/state.html
Macroscopic description
Pressure
Volume
Temperature
Microscopic description
Shape of the molecule
Bond angle
Intermolecular forces
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3
The Ideal GasA dilute gas can be modeled as consisting
of point masses that do not interact withone another.
If the pressure of helium is measured as a
function of the volume for different
values of temperature, the set of nonintersecting hyperbolas are obtained.
These curves quantitatively fit the
functional form given below.
is determined to be proportional nR.
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Gas constant = R = 8.314 J K-1mol-1 = 0.0821 L atm mol-1 K-1
Volume (V) m3
1 L = 1 dm3= 0.001 m3= 1000 cm3 = 1000 mL
1 mL = 1 cm3= 10-6 m3
Amount (n) moles
n= no. of particles / no. of particles per mole (Avogradros no.)
[Avogradros no. = 6.022 x 1023mol-1]
n= m / Mr
Temperature (T) kelvin (K) 0 C = 273.15 K
Pressure = Force (N) / Area (m2) 1 Pa = 1 Nm-2
760 mm Hg = 760 Torr = 101325 Pa = 1 atm = 1.01325 bar = 14.7 psi(lb in-2)
PV = nRT
Equation of state
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CM 1502 5
A steel tank has a volume of 438 L and is filled with 0.885 kg of O2.
Calculate the pressure (in atm) of O2at 210C.
T = 21 C = (273.15 + 21) K = 294.15K
Equation
V
n
T
PV = nRT
438 L
n = m/Mr = 885 g/32 gmol-1= 27.7 mol
Answer
P =nRT
V=
27.7 mol 294.15 K0.0821 L atm K-1mol-1x
438 L= 1.5 atm
x
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CM 1502 6
4 variables P, V, n, T
In the ideal gas law PV = nRT, there are 4 variables P, V, n and T.
Vary one property, another will change, other two are constant.
1. Increase P, V decrease, constant n and T
Boyles Law (V 1/P)
2. Increase T, V increase, constant P and n
Charless Law (V T)
3. Increase T, P increase, constant V and nAmontomss Law(P T)
4. Increase n, V increase, constant P and T
Avogradros Law (V n)
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Molar volume.
Molar volume volume taken up per 1 mole. Vm= V/n
According to Avogradros principle, Vm should be the same for all ideal gases.
Figure 5.8 CM1401
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CM 1502 9
Video
http://www.mhhe.com/physsci/chemistry/animations/chang_7e_esp/gam2s2_6.swf
Fill in the table.
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Laws defining ideal gases Description
Boyles Law V 1/P
Charless Law V T
Amontomss Law P T
Avogradros Law V n
http://www.mhhe.com/physsci/chemistry/animations/chang_7e_esp/gam2s2_6.swfhttp://www.mhhe.com/physsci/chemistry/animations/chang_7e_esp/gam2s2_6.swfhttp://www.mhhe.com/physsci/chemistry/animations/chang_7e_esp/gam2s2_6.swfhttp://www.mhhe.com/physsci/chemistry/animations/chang_7e_esp/gam2s2_6.swf -
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CM 1502 10
In an industrial process, N2enters a constant volume vessel at 300 K
and exerts a pressure of 100 atm. If it is heated to 500 K, calculate the
pressure (in atm) it will exert.
According to Amontoms Law: Increase T, P increase, constant V and n
(P T). So increase T, expect an increase in P.
22
22
11
11
22
22
11
11
Tn
VP
Tn
VPSo,
RTn
VP
andRTn
VP
RnT
PVnRTPV
=
==
=
=
atm167P
500
P
300
100
T
P
T
Pconstant,arenandVSince
2
2
2
2
1
1
=
=
=
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CM 1502 11
Gases mix homogeneously in any proportions.
Each gas in a mixture behaves as if it were the only gas present.
The pressure exerted by each gas in a mixture is calledits partial pressure.
Daltons Law of partial pressures states that the total
pressure in a mixture is the sum of the partial pressures
of the component gases.
The partial pressure of a gas is proportional to its mole
fraction:
PA= XAx Ptotal
Daltons Law of Partial Pressures
XA=nA
ntotal
Gas A
PA= 5 kPa
Gas B
PB= 20 kPa
Gas A + B
PT= PA+ PB=25 kPa
+=
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CM 1502 12
Ideal vs. Real Gases Ideal gases are assumed to have no intermolecular
interactions. Real gases have attractions and repulsions
between molecules.
Real gases behave more and more like ideal gases as
the P is reduced, identical when P = 0 as gas molecules
are too far apart to interact.
In practice, at atmospheric P at sea level (P 100 kPa),
low enough for most real gases to behave ideally.
Ideal gases particles are assumed to occupy no space.
But the assumption is valid only if V is large or [gas] is
very low
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CM 1502 13
Real Gases:
Intermolecular Interactions
Distance between gas molecules:
None/small: repulsions, increase total E of
gas => positive potential E.HIGH PRESSURE
Intermediate: attractions, decrease total E of
gas => negative potential E.MODERATE PRESSURE
Large: no interactions, potential E = 0.
LOW PRESSURE
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CM 1502 14Far apart Very near
1nRT
PV=
For 1 mole of gas
The behavior of several
real gases with increasing
external pressure.
1nRT
PV
Boyles Law:
Increase P, V decrease
V 1/P
Attractive
forces
dominate
Repulsive
forces
dominate
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CM 1502 15
Equations of State for real gases
Variations to the ideal gas law has to be made to account for
intermolecular interactions in real gases.
- Van der Waals equations of state
- Others include Virial (force), Berthelot, Dieterici equations of state.
(P +n
2a
V2 )(V nb) = nRT
Van der Waals
equation for n
moles of a real gas
n2a/V2term account for intermolecular interactions and
nb account for volume of the gas particles
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CM 1502 16
0.034
0.211
1.35
2.32
4.19
0.2441.39
1.36
6.49
3.59
2.25
4.17
5.46
He
Ne
Ar
Kr
Xe
H2N2
O2
Cl2CO2
CH4
NH3
H2O
0.0237
0.0171
0.0322
0.0398
0.0511
0.02660.0391
0.0318
0.0562
0.0427
0.0428
0.0371
0.0305
Gas
aatm*L2
mol2
bL
mol
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Van der Waals Constants for Some Common Gases
VDW
considers
both
attractive and
repulsive
forces.
Large a value : Intermolecular forces are significant
Large b value : Volume of particles is significant