Structure of Laminar Coflow Methane–Air Diffusion Flames

1986 ◽  
Vol 108 (3) ◽  
pp. 640-648 ◽  
Author(s):  
K. Saito ◽  
F. A. Williams ◽  
A. S. Gordon

Measured temperature and composition profiles are reported for a number of flames. Implications concerning flame structure are deduced, with emphasis on soot formation and on correlations involving conserved scalars.

Energies ◽  
2021 ◽  
Vol 14 (12) ◽  
pp. 3671
Author(s):  
Subrat Garnayak ◽  
Subhankar Mohapatra ◽  
Sukanta K. Dash ◽  
Bok Jik Lee ◽  
V. Mahendra Reddy

This article presents the results of computations on pilot-based turbulent methane/air co-flow diffusion flames under the influence of the preheated oxidizer temperature ranging from 293 to 723 K at two operating pressures of 1 and 3 atm. The focus is on investigating the soot formation and flame structure under the influence of both the preheated air and combustor pressure. The computations were conducted in a 2D axisymmetric computational domain by solving the Favre averaged governing equation using the finite volume-based CFD code Ansys Fluent 19.2. A steady laminar flamelet model in combination with GRI Mech 3.0 was considered for combustion modeling. A semi-empirical acetylene-based soot model proposed by Brookes and Moss was adopted to predict soot. A careful validation was initially carried out with the measurements by Brookes and Moss at 1 and 3 atm with the temperature of both fuel and air at 290 K before carrying out further simulation using preheated air. The results by the present computation demonstrated that the flame peak temperature increased with air temperature for both 1 and 3 atm, while it reduced with pressure elevation. The OH mole fraction, signifying reaction rate, increased with a rise in the oxidizer temperature at the two operating pressures of 1 and 3 atm. However, a reduced value of OH mole fraction was observed at 3 atm when compared with 1 atm. The soot volume fraction increased with air temperature as well as pressure. The reaction rate by soot surface growth, soot mass-nucleation, and soot-oxidation rate increased with an increase in both air temperature and pressure. Finally, the fuel consumption rate showed a decreasing trend with air temperature and an increasing trend with pressure elevation.


Fuel ◽  
2022 ◽  
Vol 309 ◽  
pp. 122244
Author(s):  
Andisheh Khanehzar ◽  
Francisco Cepeda ◽  
Seth B. Dworkin

2021 ◽  
Author(s):  
Armin Veshkini ◽  
Seth B. Dworkin

A numerical study is conducted of methane-air coflow diffusion flames at microgravity (μg) and normal gravity (lg), and comparisons are made with experimental data in the literature. The model employed uses a detailed gas phase chemical kinetic mechanism that includes PAH formation and growth, and is coupled to a sectional soot particle dynamics model. The model is able to accurately predict the trends observed experimentally with reduction of gravity without any tuning of the model for different flames. The microgravity sooting flames were found to have lower temperatures and higher volume fraction than their normal gravity counterparts. In the absence of gravity, the flame radii increase due to elimination of buoyance forces and reduction of flow velocity, which is consistent with experimental observations. Soot formation along the wings is seen to be surface growth dominated, while PAH condensation plays a more major role on centerline soot formation. Surface growth and PAH growth increase in microgravity primarily due to increases in the residence time inside the flame. The rate of increase of surface growth is more significant compared to PAH growth, which causes soot distribution to shift from the centerline of the flame to the wings in microgravity. Keywords: laminar diffusion flame,methane-air,microgravity, soot formation, numerical modelling


2020 ◽  
Vol 194 ◽  
pp. 04054
Author(s):  
Bencheng Zhu ◽  
Yuhan Zhu ◽  
Jiajia Wu ◽  
Kun Lu ◽  
Yang Wang ◽  
...  

This article employs the CoFlame Code to investigate the effects of hydrogen addition to fuel on soot formation characteristics in laminar coflow methane/air diffusion flames at atmospheric pressure. Numerical calculations were carried out using a detailed C1-C2 gas phase reaction mechanism and a soot model consisting of two pyrene molecules colliding into a dimer as soot nucleation, hydrogen abstraction acetylene addition (HACA) and pyrene condensation as surface growth, and soot oxidation by O2, O and OH radicals. Calculations were conducted for five levels of hydrogen addition on volume basis. To quantify the chemical effect of hydrogen, additional calculations are performed for addition of inert pseudo-hydrogen (FH2). The addition of H2 or FH2 does not have a strong influence on flame temperature. The results confirm that hydrogen addition can inhibit soot formation in the methane/air diffusion flame by reducing both the nucleation and surface growth steps of soot formation process. The effect of FH2 addition on soot formation suppression is more remarkable than H2, indicating that the chemical effect of hydrogen added to methane prompts soot formation. The dilution effect of hydrogen addition on soot formation suppression is stronger than its chemical effect on soot formation enhancement the present findings are consistent with those of previous numerical studies.


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