TY - JOUR
T1 - Structure of equilibrium reaction rate fields in turbulent jet diffusion flames
AU - Buch, Kenneth A.
AU - Dahm, Werner J.A.
AU - Dibble, Robert W.
AU - Barlow, Robert S.
N1 - Funding Information:
This work is supported in part by the Gas Research Institute (GRI) under Contract Nos. 5088-260-1443 and 5089-260-1692, and by the Air Force Office of Scientific Research (AFOSR) under Grant No. 89-0541. The conserved scalar imaging measurements were conducted with the aid of Dominique Fourguette at the Combustion Research Facility of Sandia National Laboratories (Livermore, CA), which is supported by the Department of Energy, Office of Basic Energy Sciences, Division of Chemical Science.
PY - 1992
Y1 - 1992
N2 - The structure of instantaneous chemical reaction rate field ωi(x,t) in turbulent jet diffusion flames is examined from nonreacting flow data in the limit of full chemical equilibrium. The equilibrium reaction rate fields are obtained from fully-resolved planar Rayleigh scattering imaging measurements of the instantaneous conserved scalar field ζ(x,t) in the self-similar far field of a turbulent jet flow. The resolution attained reaches below the finest local lengthscales λv and λD on which gradients in the vorticity and scalar gradient fields, respectively, can be sustained by the competing effects of strain and diffusion in the flow. Together with the signal quality achieved this allows accurate differentiation of the instantaneous scalar field data to determine the corresponding structure of the instaneous scalar energy dissipation rate fields (ReSc)-1∇ζ·∇ζ(x,t). The self-similar far-field scaling of this flow allows these data to be mapped to any downstream location, permitting a composite construction of the instantaneous equilibrium reaction rate fields throughout a turbulent jet diffusion flame. Results presented for hydrogen-air chemistry indicate that the individual species reaction rate fields are composed entirely of layer-like reaction structures. The strain-diffusion balance which sets the thickness of these structures precludes the presence of any turbulent motions within them. Moreover, whereas direct imaging measurements of OH concentration fields have suggested the presence of broad homogeneous reaction zones near the flame tip, the present OH reaction rate fields show that the reactions remain confined to these locally layer-like structures throughout the entire length of the flame.
AB - The structure of instantaneous chemical reaction rate field ωi(x,t) in turbulent jet diffusion flames is examined from nonreacting flow data in the limit of full chemical equilibrium. The equilibrium reaction rate fields are obtained from fully-resolved planar Rayleigh scattering imaging measurements of the instantaneous conserved scalar field ζ(x,t) in the self-similar far field of a turbulent jet flow. The resolution attained reaches below the finest local lengthscales λv and λD on which gradients in the vorticity and scalar gradient fields, respectively, can be sustained by the competing effects of strain and diffusion in the flow. Together with the signal quality achieved this allows accurate differentiation of the instantaneous scalar field data to determine the corresponding structure of the instaneous scalar energy dissipation rate fields (ReSc)-1∇ζ·∇ζ(x,t). The self-similar far-field scaling of this flow allows these data to be mapped to any downstream location, permitting a composite construction of the instantaneous equilibrium reaction rate fields throughout a turbulent jet diffusion flame. Results presented for hydrogen-air chemistry indicate that the individual species reaction rate fields are composed entirely of layer-like reaction structures. The strain-diffusion balance which sets the thickness of these structures precludes the presence of any turbulent motions within them. Moreover, whereas direct imaging measurements of OH concentration fields have suggested the presence of broad homogeneous reaction zones near the flame tip, the present OH reaction rate fields show that the reactions remain confined to these locally layer-like structures throughout the entire length of the flame.
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U2 - 10.1016/S0082-0784(06)80039-1
DO - 10.1016/S0082-0784(06)80039-1
M3 - Article
AN - SCOPUS:0027012248
SN - 0082-0784
VL - 24
SP - 295
EP - 301
JO - Symposium (International) on Combustion
JF - Symposium (International) on Combustion
IS - 1
ER -