TY - JOUR
T1 - NOx formation and flame velocity profiles of iso-and n-isomers of butane and butanol
AU - Chung, Gregory A.
AU - Akih-Kumgeh, Benjamin
AU - Watson, Graeme M.G.
AU - Bergthorson, Jeffrey M.
N1 - Funding Information:
The authors gratefully acknowledge support from the AUTO21 NCE and a jointly-funded initiative by NSERC, MITACS, CRIAQ and Rolls-Royce Canada.
PY - 2013
Y1 - 2013
N2 - NO formation and flame propagation are studied in premixed flames of iso- and n-isomers of butane and butanol through experimental measurements and direct simulation of experimental profiles. The stabilized flame is realized through the impingement of a premixed combustible jet from a contraction nozzle against a temperature-controlled plate. The velocity field is obtained by means of Particle Image Velocimetry (PIV) and nitric oxide concentration profiles are measured using Planar Laser Induced Fluorescence (PLIF), calibrated using known NO seeding levels. It is found that NO formation in n- and iso-isomers is comparable under the conditions considered, except for rich butanol mixtures, whereby NO formation is higher for iso-butanol. Generally, less NO is formed in butanol flames than in the butane flames. The experiment is simulated by a 1D chemically reacting stagnation flow model, using literature models of C1-C4 hydrocarbons [Wang et al., 2010] and butanol combustion chemistry [Sarathy et al., 2009, 2012]. NO prediction is tested using two of these mechanisms with a previously-published NOx submechanism added into the butane and butanol models. While a good level of agreement is observed in the velocity field prediction under lean and stoichiometric conditions, discrepancies exist under rich conditions. Greater discrepancies are observed in NO prediction, except for the C1-C4 mechanism which shows good agreement with the experiment under lean and stoichiometric conditions. The current study provides data for further development of mechanisms with NOx prediction capabilities for the fuels considered here.
AB - NO formation and flame propagation are studied in premixed flames of iso- and n-isomers of butane and butanol through experimental measurements and direct simulation of experimental profiles. The stabilized flame is realized through the impingement of a premixed combustible jet from a contraction nozzle against a temperature-controlled plate. The velocity field is obtained by means of Particle Image Velocimetry (PIV) and nitric oxide concentration profiles are measured using Planar Laser Induced Fluorescence (PLIF), calibrated using known NO seeding levels. It is found that NO formation in n- and iso-isomers is comparable under the conditions considered, except for rich butanol mixtures, whereby NO formation is higher for iso-butanol. Generally, less NO is formed in butanol flames than in the butane flames. The experiment is simulated by a 1D chemically reacting stagnation flow model, using literature models of C1-C4 hydrocarbons [Wang et al., 2010] and butanol combustion chemistry [Sarathy et al., 2009, 2012]. NO prediction is tested using two of these mechanisms with a previously-published NOx submechanism added into the butane and butanol models. While a good level of agreement is observed in the velocity field prediction under lean and stoichiometric conditions, discrepancies exist under rich conditions. Greater discrepancies are observed in NO prediction, except for the C1-C4 mechanism which shows good agreement with the experiment under lean and stoichiometric conditions. The current study provides data for further development of mechanisms with NOx prediction capabilities for the fuels considered here.
KW - Biobutanol
KW - Butane
KW - Stagnation flames
KW - Structure-reactivity
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U2 - 10.1016/j.proci.2012.06.114
DO - 10.1016/j.proci.2012.06.114
M3 - Article
AN - SCOPUS:84873356232
SN - 1540-7489
VL - 34
SP - 831
EP - 838
JO - Proceedings of the Combustion Institute
JF - Proceedings of the Combustion Institute
IS - 1
ER -