GAS LAWS
Gases exerts pressure
Pressure = Force per unit of area
P = Force (Newtons = kg m/sec2)
Area m2
Pascal (Pa) = N/m2
Barometer: measures atmospheric pressure
Manometer: measures pressure of confined gas T-78, 79
Standard press @ sea level:
1 atm = 760 mm Hg
= 29.9 in Hg
= 760 torr
= 101.325 kPa
= 14.7 psi
STP = Standard Temp and Press (273 K and 1 atm)
ALL TEMPS ARE IN KELVINS!!!!
Why? K = Co + 273
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Boyles |
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Gay-Lussac’s |
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Avogadro’s hypothesis: vol of gases @ same Temp and Press contain = # molec.
Avogadro’s Law: gas @ const temp and press, the vol of gas is α to # moles of gas
PV= nRT
R = dif. values, depending on other variables
R = 0.08206 L x atm
mol x K
R = 8.314 Joules
mol x K
Density ρ = mass
Vol
PV = nRT
Molar Mass = mass
Moles
Dalton’s Law of Partial Pressure:
Total pressure of mixture of gases is sum of its parts
P tot = P gas 1 + P gas 2 + P gas 3 + …
Corrections for gas pressure
Suppose you collect a gas over water…like diagram
P inside tube = P gas + P water vapor
If level of liquid inside is = outside liquid level
To compare atm press (in mmHg) to water pressure inside, must consider Hg is 13.6x heavier than water
Mole Fraction X
X a = moles a (certain gas)
Total moles in substance (gas)
Kinetic-Molecular Theory:
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5.
absolute temp of subst α avg. KE of particles
root-mean square (rms) u : speed of a molecule possessing the avg. KE (similar to avg speed)
ε = ˝ m u 2
ε = avg KE of the gas molecules
m = mass of the molecule
u = 3 RT R = 8.314 Joules
√ MM mol x K
Diffusion: the spreading of one substance through another (one gas through other gases)
Effusion: escape of a gas through a small hole
Which molecules will diffuse faster, He or Ar?
Can be calculated through Graham’s Law
Assume two gases @ same temp (KE are =)
˝ mHevHe2 = ˝ mArvAr2
↑ masses particles travel slower than ↓ massed molecules
Compare the rates of diffusion of oxygen to helium:
Mean Free Path: avg dist traveled by a molec. betw collisions
Diffusion of gases much slower than molecular speeds due to molec collisions
↑ density ↓ mean free path
Real vs. Ideal gases:
Ideal gases:
· assume molecules don’t take up space, no intermolecular forces between particles
· works @ low press and high temp (so molecules are far apart)
Real gases:
· @ ↑ press: molecules close together, intermolecular F attract particles AND sm vol of gas becomes signif.
o so real volume decreases
· @ ↓ temp: molecules moving slower, intermolecular F attract particles
o real volume decreases (gases liquefy)
Van der Waals Equation:
Corrections for finite volume of gas particles, attractive F betw particles
Attractive F ↑ # molec. per vol
a = magnitude of strength of attraction
L2 x atm
mol 2
Vol of gas ↓ : gas molec HAVE vol
b = amt vol particles have per mol
L
Mol
P + n2a (V - nb) = nRT
V
a and b dif for ea gas
↑ as MM ↑