AME 514 Applications of
Combustion - Fall 2008
Assignment #1
Due Monday 9/22/08, 4:30 pm, at my office (OHE
430J). If youÕre off campus, you
can fax it to 213-740-8071. DEN
students should submit through the usual channels.
Read any one of the
research papers (not review papers, not textbooks) listed in the reference
section of lectures 1 – 3.
Some suggested papers and a few others are listed below (along with the
reason I think they're important papers).
Most of these papers are available on-line or in the Science and
Engineering Library. If you
have another paper relevant to the subjects of lectures 1 – 3 that you'd
really like to read instead of one of my references because it relates to your
research or work, I'll consider it, but you'll have to get my approval in
advance. Notice that most of these papers are
somewhat older, but this is partly intentional since these papers have Òstood
the test of timeÓ at least in my opinion.
Papers written by me are off limits, because you need to be free to
criticize the paper, which you might not feel comfortable doing to my papers
(at least, if you know whatÕs good for youÉ)
Prepare a critical review of the article, not to
exceed 2 pages, structured as follows:
1.
Motivation: Why
the author(s) conducted the work
2.
Summary of the
methods and results
3.
Summary of the
conclusions
4.
Merits:
Your opinion of the merits of the work
5.
Weaknesses:
Your opinion of the shortcomings of the work
Suggestions:
á
DonÕt repeat text
that is in the paper. Summarize in
your own words – it shows me that you really do understand the paper.
á
DonÕt use buzz words
from the paper without defining them.
If you donÕt understand them and donÕt feel inclined to learn what they
are (which is ok, I donÕt expect you to understand every detail of the paper) then
leave the buzz words out! In other
words: Òeverything you say can and
will be used against youÉÓ (Sounds
harsh, but thatÕs the way real science is – anything you write in a paper
is subject to evaluation and criticism).
á
Points 1 and 5 are
the most important. Say more than
1 line about item 5, in particular.
This really shows what you learned from the paper. It also helps you to generate your own
ideas for research.
HereÕs an example of what I considered to be
a really good report from a previous year, though I would prefer the 1 - 5
format as listed above.
Report on
"Formation of Nitric Oxide in Premixed Hydrocarbon Flames" by C. P.
Fenimore, Proceedings of the
Combustion Institute, Vol. 13, p. 373, 1971.
At
the time this paper was written, the formation of nitric oxide in premixed
hydrocarbon flames had not been completely characterized. Concentrations of NO resulting from
simple N2-O2-NO combinations could be calculated but it was still uncertain how
fuel-rich flames could produce such high levels of nitric oxide. Fenimore set out to test the known laws
of NO formation in relation to hydrocarbon flames in an attempt to find a more
accurate explanation for how and where nitric oxide forms.
Experiments
were conducted on both nonadiabatic and adiabatic flames. For the nonadiabatic case, flames were
generated at atmospheric pressure by using porous plate burners which allowed
for variable reactant mixtures.
Product gasses were sampled downstream of the flame and analyzed for NO
and NO2 concentrations, which were then plotted as a total nitric oxide
concentration versus time. As the
reaction time increased, the total nitric oxide concentration increased in a
linear fashion. Since sampling at
the primary reaction zone was not possible due to the proximity of the burner
surface, Fenimore extrapolated the NO vs. time plots back to time equal to zero
in order to find qualitative observations at the reaction zone. The extrapolated intersections occurred
at NO concentrations greater than zero.
No nitric oxide was present at time zero which indicated rapid
production of NO very close to the flame after which the concentration followed
the constant linearly increasing trend obtained by the experiments.
The
adiabatic ethylene-air flames were created by using a Meker-type burner which allowed
Fenimore to vary the pressure as well as the mixture strength. As with the nonadiabatic flames, data
relating NO concentration to time were plotted and extrapolated back to time
zero. The nitric oxide
concentrations at time zero (inferred by extrapolation) show a slight increase
with pressure for fuel-rich mixtures and an even greater increase for fuel-lean
mixtures. With the newly acquired
NO concentration intercepts at time zero, a plot of the intercept versus the
mixture strength was also created.
The higher the pressure cases had intercepts corresponding to higher NO
concentrations at the primary reaction zone. The same data set was also plotted as the logarithm of the
NO concentration extrapolated intercept divided by the equilibrium NO concentration
versus the mixture strength.
Quickly formed NO (that at time zero) increased proportionally to
pressure raised to the 0.5 power.
As the mixtures reached 1.4 to 1.5 times that of a stoichiometric
mixture, the NO at the reaction zone sometimes exceeds the equilibrium
concentration.
This
work on NO formation in flames accomplished two main tasks. First, it verified the already known
mechanisms that describe nitric oxide growth in combustion product gas. The most significant aspect of the
research was showing the existence of prompt NO formation in the primary
reaction zone. Although it was not
possible to sample the gas at the primary reaction zone, Fenimore was able to
show that some amount of NO must be forming at the flame front. Without the prompt NO formation, the
nitric oxide concentration in the post-flame gas would have to be lower. Since the concentrations of NO vs. time
plots are linear, extrapolation to time zero would result in a concentration of
zero if no prompt NO formation occurred.
This was a major discovery.
At
the same time, however, Fenimore does very little to postulate by what
mechanisms prompt NO forms. Two
reactions are given that could be linked to the formation of nitric oxide in
the primary reaction zone, but no experiments are conducted in order to verify
or disprove the possibility. It
would have been beneficial to attempt to explain the formation of prompt NO
rather than just stating that it exists.
Problem #1. Flammability limits
For each of the following extinction limit
mechanisms
¥
Conduction heat losses to a tube wall
¥
Buoyancy-induced limit for upward propagation in a tube
¥
Buoyancy-induced limit for downward propagation in a tube
¥
Radiation heat loss
answer the following two questions: (1) Which would extinguish at higher SL
– CO2 or N2-diluted stoichiometric CH4-O2 mixtures?
(2) Which would extinguish at higher adiabatic flame temperature?
Problem #2. Flammability limits
a)
Explain the following experimental data taken for downward propagating flames in CH4-air mixtures
in a 5 cm diameter tube at earth gravity. At approximately what
pressure and what SL,lim would the ÒkneeÓ of this curve occur?

b)
Explain the following experimental data taken for downward propagating
flames in CH4-air mixtures in a 5 cm diameter tube at
zero-gravity. At approximately what pressure and what
SL,lim would the ÒkneeÓ of this curve occur?

Possibly useful information: g = 980 cm/sec2; Tad
Å 1500K; To Å 300K; a (air, 1 atm) = 0.2 cm2/sec; a ~ P-1; k(air, 1 atm) = 0.026 W/mK; k ~
P0; b Å 14 = constant; L of CH4-air combustion products, 1 atm)
= 106 W/m3; L ~ P1.
Problem #3. Ignition
For H2-air
mixtures with initial temperature 300K and pressure 1 atm, heating value QR
= 1.2 x 108 J/kg for hydrogen (note on the rich side that not all of
the hydrogen is consumed!!), with mixture CP = 8 cal/mole K,
a)
Calculate and plot the adiabatic flame temperature as a function of
equivalence ratio (f), assuming constant
CP and no dissociation, according to the relation QRYF
= CP(Tad – T°), where Yf is
the fuel mass fraction (which in turn is a function of the equivalence ratio f).
b)
Using the simple relation SL ~ (aW)1/2 with W ~ exp(-E/RTad), determine the
proportionality constant needed to obtain SL = 200 cm/sec at f = 1.
Assume a Å 1 cm2/sec
and E = 27 kcal/mole.
c)
From this information, calculate and plot SL and d = a/SL as a function of f.
d)
Assuming LeH2 = 0.3, LeO2 = 1.1, and using a
weighted-average Le given by
Le
= [1/(1+f)] LeH2 + [f/(1+f)] LeO2
calculate and plot the equilibrium radius of the
stationary spherical flame as a function of f.
e)
From this
information calculate and plot the minimum ignition energy as a function of f.
f)
Compare this to the
experimental results of Lewis and von Elbe. To what do you attribute the differences?
Problem #4. NO formation
a) For a stoichiometric premixed laminar methane-air
flame, plot the log of NO concentration as a function of distance from the
flame front. (Make it a big plot
since you will be drawing several other curves on the same plot.) Explain the shape of this plot briefly.
b) On the same plot, draw the NO concentration as a
function of distance from the flame front for a very lean methane-air
flame. Explain the shape of this
plot briefly.
c) Repeat b) for a stoichiometric methane-air flame
with just enough exhaust gas recirculation to have the same adiabatic flame
temperature as the flame of part b)
d) Repeat b) for a very rich methane-air flame.
e) Repeat b) for a very rich CO-air flame.
(Consider both thermal
and prompt NO formation, and the relative magnitudes of both types of NO for
each of these flames).
f) In terms of maximum NO concentration, how would a nonpremixed methane-air flame with
no fuel or air dilution compare to the premixed flames in a) – e), i.e.
which premixed flames would have a higher maximum NO, and which would have a
lower maximum NO?
Problem #5. Soot formation.
Rank each member of the following groups (rank the
members of each group separately, don't try to rank across groups) in terms of
their propensity to form soot, and explain why. For example group 1:
d, a, c, b; group 2: a, d, c, b.
Group 1:
a.
Stoichiometric
premixed methane-air flame
b.
Non-premixed
methane-air flame with no fuel or air dilution
c.
Non-premixed
methane-air flame with synthetic air having 30% O2 rather than the
usual 21%
d.
Non-premixed
ethane-air flame with no fuel or air dilution
Group 2 (all with N2 dilution
adjusted to obtain same peak temperature):
a.
Slightly rich
premixed propane-air flame (propane: H3C-CH2-CH3)
b.
Slightly rich
premixed butane-air flame (butane: H3C-CH2-CH2-CH3)
c.
Slightly rich
premixed propylene-air flame (propylene: H3C=CH-CH3)
d.
Non-premixed
propane-air flame
Group 3
a.
Slightly rich
premixed propane-air flame with no heat losses
b.
Same flame as 3a but
with substantial heat losses in burned gas
c.
Non-premixed
propane-air flame with same peak temperature as in 3a and no heat losses
d.
Same flame as in 3c
but with substantial heat losses
Problem #6. Miscellaneous
Ronney
Oil and Gas Co. claims to have invented a new fuel additive, called PDR¨,
which increases the fuel heating value (QR) by 10% but has no effect on any other chemical,
thermodynamic or transport property. Estimate by what percent each of the
following combustion properties would increase or decrease by adding PDR¨
to propane (C3H8) in each of the following cases (i.e. is
there less than 10% change, exactly 10% change, or more than 10% change). In some cases there may be no change at
all. (Again, 3 points per part,
1 part free, but do all parts in this case.)
a)
Flame-front
temperature of a non-premixed C3H8-air flame under
diffusion-controlled burning conditions
b)
Extinction stretch
rate of a premixed C3H8-air flame
c)
The burning velocity
at the downward flammability limit
(SL,lim) of a lean premixed C3H8-air flame in
a large diameter tube.
d)
The burning velocity
at the radiation-induced flammability limit (SL,lim) of a lean premixed C3H8-air
flame with negligible buoyancy effects
e)
The adiabatic flame
ball radius in a stoichiometric premixed C3H8-air mixture
f)
The amount of soot
production in a rich premixed C3H8-air flame at
equivalence ratio 1.4
g)
The amount of soot
production in a nonpremixed laminar C3H8 jet flame
h)
Amount of prompt NO
in the products of a rich premixed C3H8-air flame at
equivalence ratio 1.4, far downstream of the flame where chemical equilibrium
is reached, with N2 added to obtain the same adiabatic flame
temperature as a C3H8-air mixture without PDR¨
additive