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RESEARCH POSTER PRESENTATION DESIGN © 2012
www.PosterPresentations.com
The qualitative notion that ignition processes have similar behavior, even
over an extensive range of starting conditions, is quantitatively
demonstrated through the production of a single ’generic’ ignition curve.
The key to the production of the generic curve is the recognition that the
basic shapes of the species and temperature profiles occurring in the
ignition process differ only in their ’timing’. By ’morphing’ the time scale,
the profile shapes can be made to align. From the aligned profile shapes a
generic or ’average’ profile can be derived. Synchronizing chemical events
modifies the ignition progress times. In addition to fixing the ignition time
to have the progress value of one, intermediate ignition events (such as
selected profile maxima or inflection points) that occur before ignition are
also aligned to have specific ’normalized’ times.
Abstract	
  
Synchroniza@on	
  
Time	
  Devia@ons	
  from	
  Linear	
  
Mul@ple	
  Synchroniza@ons	
  
Generic	
  Curves	
  
The inherent assumption is that a given progress value, regardless of its
origin, should represent a given stage of the ignition process. In terms of
species profiles, for example, this means that a given species reaches a
maxima at the same progress value regardless of starting conditions. The
one assumption is that relatively the same mechanistic steps are involved.
Different mechanistic steps would imply another generic curve.
Edward	
  S.	
  Blurock,	
  REACTION,	
  Sweden	
  
Characterizing	
  Igni@on	
  behavior	
  through	
  morphing	
  to	
  
generic	
  curves	
  
	
  
This work exploits
the similarities of an ignition process
to produce generic ignition curves,
uniting ignition curves,
each with different starting conditions,
into one common behavior
using one single progress variable.
0 0.0005 0.001 0.0015
Ignition Process Time (s)
1000
1500
2000
2500
3000
Temperature(Kelvin)
0 0.0005 0.001
Ignition Process Time (s)
0
0.001
0.002
0.003
0.004
0.005
0.006
0.007
MassFractionofSpecies
CH2O
H2O2
HO2
CHO
0 1 2
Normalized Time (Ignition at 1.0)
1000
1500
2000
2500
3000
Temperature(Kelvin)
0.50
0.75
1.00
0 0.5 1
Normalized Time (Ignition at 1.0)
0
0.001
0.002
0.003
0.004
0.005
0.006
0.007
SpeciesMassFractions
CH2O
H2O2
HO2
CHO
0 0.2 0.4 0.6 0.8 1
Normalized Time (both with T and H2O2 max)
0
0.0005
0.001
0.0015
0.002
MassFractions
O.50
0.75
1.00
Equivalence Ratio
H2O2 Max Time Norm
0 0.2 0.4 0.6 0.8 1
Normalized Time (with both T and H2O2 Max)
0
0.2
0.4
0.6
0.8
1
NormalizedMassFraction
0.50
0.75
1.00
Equivalence Ratio
All	
  figures	
  show	
  a	
  range	
  of	
  condi/ons,	
  with	
  3	
  star/ng	
  temperatures	
  (1200,	
  1250,	
  1300	
  Kelvin),	
  two	
  
star/ng	
  pressures	
  (1,11	
  atm)	
  and	
  three	
  different	
  equivalence	
  ra/os	
  (0.50,	
  0.75,	
  1.00.	
  The	
  first	
  is	
  a	
  plot	
  of	
  
the	
  H2O2	
  with	
  a	
  /me	
  normaliza/on	
  at	
  both	
  the	
  maximum	
  of	
  the	
  H2O2	
  mole	
  frac/on	
  (derived	
  from	
  the	
  
average	
  of	
  the	
  set,	
  0.745)	
  and	
  at	
  the	
  igni/on	
  /me	
  (1.0).The	
  second	
  is	
  with	
  the	
  H2O2	
  maximum	
  
normalized	
  to	
  1.0.	
  
A	
  set	
  of	
  igni/on	
  curves	
  where	
  the	
  /me	
  is	
  normalized	
  to	
  be	
  at	
  the	
  point	
  of	
  igni/on.	
  The	
  first	
  curve	
  is	
  /me	
  
versus	
  temperature	
  with	
  5	
  different	
  star/ng	
  temperatures	
  from	
  1200	
  to	
  1300	
  and	
  three	
  different	
  
equivalence	
  ra/os	
  (see	
  legend).	
  The	
  second	
  curve	
  shows	
  the	
  evolu/on	
  of	
  intermediate	
  species	
  at	
  ten	
  
star/ng	
  temperatures	
  between	
  1200	
  and	
  1300	
  Kelvin.	
  Only	
  values	
  several	
  (20	
  /mes	
  10{-­‐5)	
  past	
  igni/on	
  were	
  
calculated.	
  For	
  some	
  star/ng	
  condi/ons,	
  the	
  equilibrium	
  was	
  not	
  reached.	
  
0 0.2 0.4 0.6 0.8 1
Normalized Time
-0.02
-0.01
0
0.01
0.02
0.03
Deviation
0.5
0.6
0.7
0.8
0.9
1.0
0 0.2 0.4 0.6 0.8 1
Normalized Time
-0.05
0
0.05
Deviation
1200K
1210K
1220K
1230K
1240K
1250K
1260K
1270K
1280K
1290K
1300K
The	
  devia/on	
  from	
  linear	
  progression	
  based	
  only	
  on	
  igni/on	
  /me.	
  Four	
  events	
  (see	
  text)	
  were	
  chosen	
  as	
  /me	
  
normaliza/on	
  points.	
  The	
  graphs	
  show	
  the	
  devia/ons	
  along	
  the	
  normalized	
  /me	
  for	
  a	
  (le]	
  graph)	
  a	
  range	
  of	
  
temperatures,	
  1200K	
  to	
  1300K	
  (1	
  atmosphere	
  pressure	
  and	
  equivalence	
  ra/o	
  of	
  1.0),	
  and	
  (right	
  graph)	
  a	
  range	
  of	
  
equivalence	
  ra/os,	
  0.5	
  to	
  1.0	
  (Temperature	
  130	
  and	
  pressure	
  1	
  atmosphere).}	
  
0 0.2 0.4 0.6 0.8 1
Temperature Normalized Progress
0
0.2
0.4
0.6
0.8
1
CH2
ONormalizedtoMaximum
0.50
0.75
1.00
0 0.2 0.4 0.6 0.8 1
Time Normalized (T, H2O2 Max)
0
0.2
0.4
0.6
0.8
1
NormalizedtoMaximum
0.50
0.75
1.00
0 0.2 0.4 0.6 0.8 1
Time Normalized (T, H2O2 Max, CH2O Max)
0
0.2
0.4
0.6
0.8
1
NormalizedtoMaximum
0.50
0.75
1.00
1 atm
11 atm
The	
  effect	
  of	
  progression	
  of	
  /me	
  normaliza/on	
  on	
  the	
  maximum	
  normalized	
  mass	
  frac/on	
  curves	
  of	
  CH2O	
  are	
  
shown.	
  	
  With	
  each	
  addi/onal	
  normaliza/on,	
  the	
  spread	
  of	
  curves	
  diminishes.	
  From	
  just	
  igni/on	
  /me	
  (le]),	
  adding	
  
H2O2	
  maximum	
  (center),	
  to	
  adding	
  both	
  H2O2	
  and	
  HO2	
  maximum	
  (right).	
  	
  All	
  figures	
  show	
  a	
  range	
  of	
  condi/ons,	
  
with	
  3	
  star/ng	
  temperatures	
  (1200,	
  1250,	
  1300	
  Kelvin),	
  two	
  star/ng	
  pressures	
  (1,11	
  atm)	
  and	
  three	
  different	
  
equivalence	
  ra/os	
  (0.50,	
  0.75,	
  1.00).	
  
0 0.2 0.4 0.6 0.8 1
Normalized Time
0
0.2
0.4
0.6
0.8
1
NormalizedH2
O2
0 0.2 0.4 0.6 0.8 1
Normalized Time
0
0.2
0.4
0.6
0.8
1
NormalizedHO2
Range	
  of	
  Validity	
  and	
  the	
  Choice	
  of	
  Events	
  
A	
  single	
  generic	
  curve	
  is	
  produced	
  by	
  morphing	
  the	
  individual	
  curves	
  to	
  coincide	
  at	
  specified	
  sequen/al	
  chemical	
  
events.	
  This	
  is	
  a	
  mathema/cal	
  descrip/on	
  of	
  the	
  statement	
  that	
  the	
  set	
  of	
  igni/on	
  curves	
  have	
  the	
  same	
  
mechanis/c	
  chemistry.	
  A	
  combus/on	
  process	
  undergoing	
  a	
  different	
  set	
  of	
  mechanis/c	
  events	
  should	
  be	
  
described	
  by	
  a	
  different	
  generic	
  curve.	
  In	
  this	
  formula/on	
  a	
  different	
  set	
  of	
  mechanis/c	
  events	
  is	
  defined	
  as	
  being	
  
a	
  set	
  of	
  curves	
  in	
  which	
  the	
  set	
  of	
  chemical	
  events	
  occur	
  and	
  occur	
  in	
  the	
  same	
  order.	
  This	
  can	
  be	
  used	
  as	
  a	
  
criteria	
  for	
  differen/a/ng	
  combus/on	
  events	
  with	
  different	
  mechanis/c	
  steps.	
  A	
  complete	
  descrip/on	
  of	
  a	
  
combus/on	
  process	
  over	
  the	
  complete	
  set	
  of	
  ranges	
  would	
  be	
  described	
  by	
  a	
  set	
  of	
  generic	
  curves.	
  
0 0.2 0.4 0.6 0.8 1
Normalized Time
-0.2
-0.1
0
0.1
0.2
DifferenceFromAverage
0 0.2 0.4 0.6 0.8 1
Normalized Time
-0.02
-0.01
0
0.01
0.02
0.03
DifferenceFromPiecewisePolynomial
The	
  le]	
  plot	
  shows	
  the	
  difference	
  between	
  the	
  average	
  generic	
  curve	
  and	
  the	
  actual	
  curves	
  of	
  the	
  individual	
  
star/ng	
  condi/ons.	
  The	
  le]	
  plot	
  shows	
  differences	
  between	
  the	
  piecewise	
  second	
  degree	
  polynomial	
  
approxima/on	
  of	
  the	
  curve	
  differences.	
  The	
  solid	
  lines	
  denote	
  minimum	
  and	
  maximum	
  values	
  and	
  the	
  doaed	
  
lines	
  between	
  are	
  the	
  difference	
  values.	
  
Towards	
  Parameteriza@on	
  
Average,	
  maximum	
  and	
  minimum	
  value	
  plots	
  of	
  HO2	
  (le])	
  and	
  H2O2	
  (right)	
  under	
  a	
  wider	
  range	
  of	
  pressures	
  
(1,11,21,31	
  atms),	
  temperatures	
  (1200-­‐1300K	
  at	
  10K	
  intervals)	
  and	
  equivalence	
  ra/os	
  (0.5,0.75	
  and	
  1.00)	
  are	
  
shown.	
  The	
  solid	
  lines	
  are	
  /me	
  normalized	
  with	
  four	
  fixed	
  points,	
  including	
  igni/on	
  /me	
  and	
  the	
  doaed	
  lines	
  is	
  
normalized	
  /me	
  with	
  respect	
  to	
  just	
  igni/on	
  /me.	
  
0.5 0.6 0.7 0.8 0.9 1
Equivalence Ratio
-0.02
-0.01
0
0.01
0.02
0.03
Deviation
0.77
0.21
0.86
0.94
1200 1220 1240 1260 1280 1300
Starting Temperature
-0.05
0
0.05
Deviation
0.23
0.78
0.88
0.93
The	
  devia/on	
  from	
  linear	
  progression	
  based	
  only	
  on	
  igni/on	
  /me.	
  Four	
  events	
  (see	
  text)	
  were	
  chosen	
  as	
  /me	
  
normaliza/on	
  points.	
  The	
  graphs	
  show	
  the	
  devia/ons	
  along	
  the	
  normalized	
  /me	
  for	
  a	
  (le]	
  graph)	
  a	
  range	
  of	
  
temperatures,	
  1200K	
  to	
  1300K	
  (1	
  atmosphere	
  pressure	
  and	
  equivalence	
  ra/o	
  of	
  1.0),	
  and	
  (right	
  graph)	
  a	
  range	
  of	
  
equivalence	
  ra/os,	
  0.5	
  to	
  1.0	
  (Temperature	
  1300	
  and	
  pressure	
  1	
  atmosphere).	
  

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Poster: Characterizing Ignition behavior through morphing to generic curves

  • 1. RESEARCH POSTER PRESENTATION DESIGN © 2012 www.PosterPresentations.com The qualitative notion that ignition processes have similar behavior, even over an extensive range of starting conditions, is quantitatively demonstrated through the production of a single ’generic’ ignition curve. The key to the production of the generic curve is the recognition that the basic shapes of the species and temperature profiles occurring in the ignition process differ only in their ’timing’. By ’morphing’ the time scale, the profile shapes can be made to align. From the aligned profile shapes a generic or ’average’ profile can be derived. Synchronizing chemical events modifies the ignition progress times. In addition to fixing the ignition time to have the progress value of one, intermediate ignition events (such as selected profile maxima or inflection points) that occur before ignition are also aligned to have specific ’normalized’ times. Abstract   Synchroniza@on   Time  Devia@ons  from  Linear   Mul@ple  Synchroniza@ons   Generic  Curves   The inherent assumption is that a given progress value, regardless of its origin, should represent a given stage of the ignition process. In terms of species profiles, for example, this means that a given species reaches a maxima at the same progress value regardless of starting conditions. The one assumption is that relatively the same mechanistic steps are involved. Different mechanistic steps would imply another generic curve. Edward  S.  Blurock,  REACTION,  Sweden   Characterizing  Igni@on  behavior  through  morphing  to   generic  curves     This work exploits the similarities of an ignition process to produce generic ignition curves, uniting ignition curves, each with different starting conditions, into one common behavior using one single progress variable. 0 0.0005 0.001 0.0015 Ignition Process Time (s) 1000 1500 2000 2500 3000 Temperature(Kelvin) 0 0.0005 0.001 Ignition Process Time (s) 0 0.001 0.002 0.003 0.004 0.005 0.006 0.007 MassFractionofSpecies CH2O H2O2 HO2 CHO 0 1 2 Normalized Time (Ignition at 1.0) 1000 1500 2000 2500 3000 Temperature(Kelvin) 0.50 0.75 1.00 0 0.5 1 Normalized Time (Ignition at 1.0) 0 0.001 0.002 0.003 0.004 0.005 0.006 0.007 SpeciesMassFractions CH2O H2O2 HO2 CHO 0 0.2 0.4 0.6 0.8 1 Normalized Time (both with T and H2O2 max) 0 0.0005 0.001 0.0015 0.002 MassFractions O.50 0.75 1.00 Equivalence Ratio H2O2 Max Time Norm 0 0.2 0.4 0.6 0.8 1 Normalized Time (with both T and H2O2 Max) 0 0.2 0.4 0.6 0.8 1 NormalizedMassFraction 0.50 0.75 1.00 Equivalence Ratio All  figures  show  a  range  of  condi/ons,  with  3  star/ng  temperatures  (1200,  1250,  1300  Kelvin),  two   star/ng  pressures  (1,11  atm)  and  three  different  equivalence  ra/os  (0.50,  0.75,  1.00.  The  first  is  a  plot  of   the  H2O2  with  a  /me  normaliza/on  at  both  the  maximum  of  the  H2O2  mole  frac/on  (derived  from  the   average  of  the  set,  0.745)  and  at  the  igni/on  /me  (1.0).The  second  is  with  the  H2O2  maximum   normalized  to  1.0.   A  set  of  igni/on  curves  where  the  /me  is  normalized  to  be  at  the  point  of  igni/on.  The  first  curve  is  /me   versus  temperature  with  5  different  star/ng  temperatures  from  1200  to  1300  and  three  different   equivalence  ra/os  (see  legend).  The  second  curve  shows  the  evolu/on  of  intermediate  species  at  ten   star/ng  temperatures  between  1200  and  1300  Kelvin.  Only  values  several  (20  /mes  10{-­‐5)  past  igni/on  were   calculated.  For  some  star/ng  condi/ons,  the  equilibrium  was  not  reached.   0 0.2 0.4 0.6 0.8 1 Normalized Time -0.02 -0.01 0 0.01 0.02 0.03 Deviation 0.5 0.6 0.7 0.8 0.9 1.0 0 0.2 0.4 0.6 0.8 1 Normalized Time -0.05 0 0.05 Deviation 1200K 1210K 1220K 1230K 1240K 1250K 1260K 1270K 1280K 1290K 1300K The  devia/on  from  linear  progression  based  only  on  igni/on  /me.  Four  events  (see  text)  were  chosen  as  /me   normaliza/on  points.  The  graphs  show  the  devia/ons  along  the  normalized  /me  for  a  (le]  graph)  a  range  of   temperatures,  1200K  to  1300K  (1  atmosphere  pressure  and  equivalence  ra/o  of  1.0),  and  (right  graph)  a  range  of   equivalence  ra/os,  0.5  to  1.0  (Temperature  130  and  pressure  1  atmosphere).}   0 0.2 0.4 0.6 0.8 1 Temperature Normalized Progress 0 0.2 0.4 0.6 0.8 1 CH2 ONormalizedtoMaximum 0.50 0.75 1.00 0 0.2 0.4 0.6 0.8 1 Time Normalized (T, H2O2 Max) 0 0.2 0.4 0.6 0.8 1 NormalizedtoMaximum 0.50 0.75 1.00 0 0.2 0.4 0.6 0.8 1 Time Normalized (T, H2O2 Max, CH2O Max) 0 0.2 0.4 0.6 0.8 1 NormalizedtoMaximum 0.50 0.75 1.00 1 atm 11 atm The  effect  of  progression  of  /me  normaliza/on  on  the  maximum  normalized  mass  frac/on  curves  of  CH2O  are   shown.    With  each  addi/onal  normaliza/on,  the  spread  of  curves  diminishes.  From  just  igni/on  /me  (le]),  adding   H2O2  maximum  (center),  to  adding  both  H2O2  and  HO2  maximum  (right).    All  figures  show  a  range  of  condi/ons,   with  3  star/ng  temperatures  (1200,  1250,  1300  Kelvin),  two  star/ng  pressures  (1,11  atm)  and  three  different   equivalence  ra/os  (0.50,  0.75,  1.00).   0 0.2 0.4 0.6 0.8 1 Normalized Time 0 0.2 0.4 0.6 0.8 1 NormalizedH2 O2 0 0.2 0.4 0.6 0.8 1 Normalized Time 0 0.2 0.4 0.6 0.8 1 NormalizedHO2 Range  of  Validity  and  the  Choice  of  Events   A  single  generic  curve  is  produced  by  morphing  the  individual  curves  to  coincide  at  specified  sequen/al  chemical   events.  This  is  a  mathema/cal  descrip/on  of  the  statement  that  the  set  of  igni/on  curves  have  the  same   mechanis/c  chemistry.  A  combus/on  process  undergoing  a  different  set  of  mechanis/c  events  should  be   described  by  a  different  generic  curve.  In  this  formula/on  a  different  set  of  mechanis/c  events  is  defined  as  being   a  set  of  curves  in  which  the  set  of  chemical  events  occur  and  occur  in  the  same  order.  This  can  be  used  as  a   criteria  for  differen/a/ng  combus/on  events  with  different  mechanis/c  steps.  A  complete  descrip/on  of  a   combus/on  process  over  the  complete  set  of  ranges  would  be  described  by  a  set  of  generic  curves.   0 0.2 0.4 0.6 0.8 1 Normalized Time -0.2 -0.1 0 0.1 0.2 DifferenceFromAverage 0 0.2 0.4 0.6 0.8 1 Normalized Time -0.02 -0.01 0 0.01 0.02 0.03 DifferenceFromPiecewisePolynomial The  le]  plot  shows  the  difference  between  the  average  generic  curve  and  the  actual  curves  of  the  individual   star/ng  condi/ons.  The  le]  plot  shows  differences  between  the  piecewise  second  degree  polynomial   approxima/on  of  the  curve  differences.  The  solid  lines  denote  minimum  and  maximum  values  and  the  doaed   lines  between  are  the  difference  values.   Towards  Parameteriza@on   Average,  maximum  and  minimum  value  plots  of  HO2  (le])  and  H2O2  (right)  under  a  wider  range  of  pressures   (1,11,21,31  atms),  temperatures  (1200-­‐1300K  at  10K  intervals)  and  equivalence  ra/os  (0.5,0.75  and  1.00)  are   shown.  The  solid  lines  are  /me  normalized  with  four  fixed  points,  including  igni/on  /me  and  the  doaed  lines  is   normalized  /me  with  respect  to  just  igni/on  /me.   0.5 0.6 0.7 0.8 0.9 1 Equivalence Ratio -0.02 -0.01 0 0.01 0.02 0.03 Deviation 0.77 0.21 0.86 0.94 1200 1220 1240 1260 1280 1300 Starting Temperature -0.05 0 0.05 Deviation 0.23 0.78 0.88 0.93 The  devia/on  from  linear  progression  based  only  on  igni/on  /me.  Four  events  (see  text)  were  chosen  as  /me   normaliza/on  points.  The  graphs  show  the  devia/ons  along  the  normalized  /me  for  a  (le]  graph)  a  range  of   temperatures,  1200K  to  1300K  (1  atmosphere  pressure  and  equivalence  ra/o  of  1.0),  and  (right  graph)  a  range  of   equivalence  ra/os,  0.5  to  1.0  (Temperature  1300  and  pressure  1  atmosphere).