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Q 1 . Ventilation gases from underground coal mines contain methane. In the development stages of a mine, methane concentration in ventilation gases can be

Q1. Ventilation gases from underground coal mines contain methane. In the development
stages of a mine, methane concentration in ventilation gases can be high and this is a major
risk with explosions possible. Unfortunately, there are many mine disasters where this has
occurred. During the operational stage of a mine, the ventilation should be sufficient to keep
the vv% of methane below explosive limits (5-15vv%) and the mine workers safe from
the risk of methane gas explosions. Even though the vv% of methane in ventilation streams is
low (typically 1vv% or less), it is a major contributor to methane emissions and greenhouse
emissions more broadly. One way to reduce greenhouse gas emissions is catalytic oxidation of
methane (remember greenhouse potential of methane is much greater than carbon dioxide).
CH4(g)+2O2(g)CO2(g)+2H2O(g)
Why catalytic oxidation and not simply burning the methane? Because methane is below the
flammability limit of 5vv% so will not burn (same reason it is safe from explosions). This
reaction is irreversible and, when the concentration of methane is very low, behaves like a
first order reaction with respect to methane on the catalyst surface.
A catalyst is being tested for catalytic oxidation of methane. The catalyst particle is porous
with a diameter of 6mm, a solid density of 2.2gcm3, a surface area of 200m2g, and a
porosity of 0.4. This catalyst is packed into a bed and has a bed voidage of 0.35. The bed is fed
with 0.5vv% of methane with the rest being air.
a) If the conversion of methane is 98.9% with a residence time of 2 seconds, what is the
effective rate constant for this reaction on a bed volume basis, in ?-1)?
b) What is the effective rate constant on a mass of catalyst basis, ke'(in L/kg.s), and on a
catalyst surface area basis, ke''(in Lm2.s)?
c) When the flowrate is increased by a factor of 10, conversion drops to 40%. If external
mass transfer resistance is negligible at this flowrate, and other assumptions from part
(a) still hold, what is the surface rate constant, ks''(in Lm2.s)?
d) What is the mass transfer coefficient at the conditions in part(a),km(in ms)? You can
use the result from the lecture notes:
ke=ks''kmSgp(1-b)km+13ks''Sgprp
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