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## Journal of the Brazilian Society of Mechanical Sciences and Engineering

##
*Print version* ISSN 1678-5878

### J. Braz. Soc. Mech. Sci. & Eng. vol.34 no.2 Rio de Janeiro Apr./June 2012

#### http://dx.doi.org/10.1590/S1678-58782012000200002

**TECHNICAL PAPERS THERMAL SCIENCES**

**Comparison of spectral models in the computation of radiative heat transfer in participating media composed of gases and soot **

**Anderson Mossi ^{I}; Marcelo M. Galarça^{II}; Rogério Brittes^{III}; Horácio A. Vielmo^{IV}; Francis H. R. França^{V}**

^{I}Federal University of Fronteira Sul. 99700-000 Erechim, RS, Brazil

^{II}marcelo.galarca@riogrande.ifrs.edu.br. Federal Institute of Education Science and Technology of Rio Grande do Sul. 96201-460 Rio Grande, RS, Brazil

^{III}rogeriobrittes@mecanica.ufrgs.br. Federal University of Rio Grande do Sul. Department of Mechanical Engineering. 90050-170 Porto Alegre, RS, Brazil

^{IV}vielmoh@mecanica.ufrgs.br. Federal University of Rio Grande do Sul. Department of Mechanical Engineering. 90050-170 Porto Alegre, RS, Brazil

^{V}frfranca@mecanica.ufrgs.br. Federal University of Rio Grande do Sul. Department of Mechanical Engineering. 90050-170 Porto Alegre, RS, Brazil

**ABSTRACT**

Accurate combustion models are necessary to predict, among other effects, the production of pollutant gases and the heat transfer. As an important part of the combustion modeling, thermal radiation is often the dominant heat transfer mechanism, involving absorption and emission from soot and participating gases, such as water vapor and carbon dioxides. If the radiative heat transfer is not accurately predicted, the solution can lead to poor prediction of the temperature field and of the formation and distribution of the gases and soot. The modeling of the absorption coefficient of the gases is a very complex task due to its highly irregular dependence on the wavenumber. On the other hand, the absorption coefficient of the soot is known to behave linearly with the wavenumber, allowing for a simpler approach. Depending on the amount of soot, the more sophisticated and expensive gas models can be replaced by simpler ones, without considerable loss of accuracy. In this study, the radiative heat transfer for a medium composed of water vapor, carbon dioxide and soot is computed with the gray gas (GG), the weighted-sum-of-gray-gases model (WSGG), and the cumulative wavenumber (CW) models. The results are compared to benchmark line-by-line (LBL) calculations.

**Keywords: **radiative heat transfer, spectral gas models, soot radiation

**Introduction **

The energy necessary to sustain the energy demand from industry and society is provided mostly by the combustion of hydrocarbons. However, environmental concerns with the pollution of gases emitted during the process require that new techniques are developed to control and reduce the levels of pollution. As such, accurate modeling of the soot formed in the process is important, because it strongly affects the temperature field and, in turn, the concentration of emitted gases, which is highly dependent on the temperature. In radiative heat transfer, emission from soot can be dominant, so the absorption and the emission from the participating gases, such as water vapor and carbon dioxide, may not play an important role when soot is present in a sufficient amount.

In the last few years, there has been a growing effort to predict the soot formation in combustion process. The main mechanisms of soot life are the nucleation, surface growth, agglomeration, and oxidation. Moss et al. (1988) proposed a model based on the premise that the soot reaction rates could be specified in terms of the mixture fraction. Experiments demonstrated that the acetylene is responsible for the surface growth and that the polycyclic aromatic hydrocarbons (PAH) initiate the soot nucleation. The oxidation is performed mainly by the OH particles, but O_{2} molecules are important in this process and have to be considered. Fairweather et al. (1992) subsequently proposed a simplified two-equation model for soot, where their model contains rate process for the nucleation, surface growth, agglomeration and oxidation. Experiments made by Sunderland et al. (1995) showed that the parameters used by Fairweather et al. (1992) are overestimated, which could result in a serious mistake in the amount of smoke produced by the flame. Wang et al. (2005) applied two radiation models to an oxygen-enriched, propane-fueled, turbulent, non-premixed jet flame. The results showed that soot and spectrally radiating gas-phase species were distributed separately in the flame, and this segregation of radiating media strongly affected the radiative heat flux, flame structure and flame temperature. A numerical study of combustion in a liquid rocket engine was performed by Byun and Baek (2007). The simulation considered spray combustion at all speeds in the rocket engine with a non-gray finite-volume radiation model to investigate the radiation effect in turbulent combustion conditions, adding the soot formation and its effect on the radiation and flow field. Liu et al. (2004) studied the effects of radiation and the individual influence of gas and soot radiation on soot formation in counterflow C2H4SF diffusion flames by comparing the numerical results against available experimental data in the literature. On the other hand, gas models have been developed since the 1960's, although the problem to compute radiation in gases can hardly be described as well as understood due to the highly complex dependence of the absorption coefficient of gases with the wavenumber spectrum. A discussion of the state of the art of gas modeling can be found in Galarça et al. (2011).

Soot emits a considerable amount of radiation in comparison to water vapor and carbon dioxide, and changes the temperature distribution, the concentration and formation of all chemical species involved in the process. This justifies the importance of an accurate modeling of radiation in media composed of soot and participating gases. In this work, it is analyzed the use of different gas models to compute the radiative heat transfer in a medium composed of water vapor, carbon dioxide and soot. Three gas models are considered: gray gas (GG), weighted-sum-of-gray-gas (WSGG) and cumulative wavenumber (CW). The main goal is to evaluate how the radiation models behave with a mixture of gases and soot, considering different amounts of soot in the medium. The results are compared with the line-by-line spectral integration of the absorption coefficient, which can be considered the benchmark solution. The spectral data for water vapor, carbon dioxide and soot is obtained either from commonly employed engineering correlations or from detailed spectral database.

**Nomenclature **

*a _{j} = j-th gray gas corresponding blackbody weight, *

*dimensionless*

*b _{j} = polynomial coefficients of the WSGG model, units can vary *

*C = absorption cross-section, m*^{2}*/molecule *

*D _{ij} = fractional gray gas, cm*

^{-1 }

*E _{b} = blackbody total emissive power, W/m*

^{2 }

*E _{b}*

_{η}

*=blackbodyspectral emissive power, W/(m*

^{2}µ

*m)*

*f _{v} = soot volumetric fraction, dimensionless *

*H = Heaviside step-function, dimensionless *

*H _{j} = wavenumber interval, cm*

^{-1 }

*I = total radiative intensity, W/m*^{2 }

*I*_{η} *= spectral radiative intensity, W/(m*^{2 }*cm ^{-1})*

*J _{ij} = fractional gray gas intensity, W/m*

^{2}

**n ***= vector normal to the surface element, dimensionless *

*N = molecular density, molecule/m*^{3 }

*P = pressure, N/m*^{2 }

*q _{R} = radiative heat flux, W/m*

^{2}

_{R }*= radiative heat source, W/m*^{3 }

max(_{R}) = *maximum radiative heat source, W/m ^{3}*

*r = number of species, dimensionless*

* s = distance traveled by the radiation intensity, m*

**s ***= vector in the direction of the radiation intensity, dimensionless*

* S _{i} = integrated intensity of line i, in (molecule cm*

^{-2}

*)*

^{-1}

*T = temperature, K*

* u _{ij} = function of the cumulative wavenumber method, dimensionless*

* v _{ij} = function of the cumulative wavenumber method, dimensionless*

* w = cumulative wavenumber function, dimensionless*

* x = position, m*

* Y = molar fraction, dimensionless *

**Greek Symbols **

γ *= half-width, cm*^{-1}*/atm*

Δ *= error, %*

Δ_{i} = wavenumber interval, cm^{-1}

ε *= surface emissivity, dimensionless*

η *= wavenumber, cm*^{-1}

κ *= absorption coefficient, m*^{-1}

κ' *= absorption coefficient per unit of partial pressure, m*^{-1 }*atm*^{-1}

τ *= optical thickness, dimensionless*

Ω *= solid angle, sr *

**Subscripts **

air *= relative to air*

avg *= relative to the average value*

* b = relative to blackbody*

* g = relative to any gas*

* i = relative to a spectral line i*

* j = relative to j-th partial gray gas*

max *= relative to the maximum value*

ref *= relative to the reference temperature*

*s = relative to soot*

self *= relative to self-broadening*

*w = relative to wall surface *

**The Absorption Coefficient of Participating Gases and Soot**

The absorption coefficient of participating gases is known by its strongly irregular variation with the wavenumber. According to Siegel and Howell (2002), for engineering applications, the absorption coefficient of the gases, κ_{η}, can be obtained with the Lorentz collision profile, given by:

where η is the wavenumber, *N *is the molar density of the absorbing species, *C*_{η} is the absorption cross-section, *S _{i} *is the integrated intensity of line

*i*, η

*is the line location, and γ*

_{i}*is the half-width given by:*

_{i}where *Y *is the molar fraction of the absorbing species, *T *is the temperature, γ_{self} is the self-broadening, γ_{air} is the air broadening half-width.

The parameters required to obtain the spectral absorption crosssection can be obtained from databases such as HITRAN and HITEMP. For water vapor and carbon dioxide at high temperatures, the most appropriate database is the HITEMP, which is obtained for temperatures of 1000 and 1500 K. This means that extrapolation of the temperature for higher values will be more accurate when compared to extrapolation with data from HITRAN, which is obtained for a temperature of 296 K. Figure 1 shows the absorption coefficient for 10% H_{2}O at 2000 K, depicting its characteristically complex dependence on the wavenumber. It should be observed that the figure presents only a narrow interval of wavenumber, 4000 cm^{-1 }__<__ η __<__ 4020 cm^{-1 }. The entire wavenumber spectrum is formed by thousands of spectral lines, so that the spectral integration of the radiative transfer requires models to obtain solutions with a reasonable computational effort.

On the other hand, experiments have demonstrated that the variation of the absorption coefficient of soot with the wavenumber can be approximated by a linear relation. One well known relation was proposed in Hottel and Sarofim (1967):

Equation (3) conveys that the dependence of the absorption coefficient with soot volumetric fraction, *f*_{ν}, is much less complex than the behavior depicted in Fig. 1. Moreover, even in small quantities, soot radiation can be dominant over the radiation from gases, so one question that arises is: how accurate does the modeling of the participating gases need to be when the total radiation involves also the contribution of soot? Answering this question is the main goal of this paper.

**Radiation Heat Transfer Modeling**

The radiative transfer equation (RTE) for non-scattering media is given by:

where *I*_{η} is the spectral radiation intensity, *s *is the distance traveled by the radiation and *I _{b}*

_{η}is the spectral intensity of radiation from a blackbody. In the right-hand side of the above equation, the first and second terms correspond, respectively, to the increase and decrease of the spectral radiation intensity due to absorption and emission in the medium. It should be noticed that the above equation neglects scattering of thermal radiation, since scattering from soot is negligible in comparison to its absorption and emission. Participating gases such as water vapor and carbon dioxide do not scatter. Equation (4) is subjected to the boundary conditions at the walls:

where ε* _{w} *is the emissivity of a diffuse gray surface, Ω is the solid angle,

**n**is the vector normal to the surface (outward) and

**n**·

**s**is the cosine of the angle between any incoming direction

**s**and the surface normal. In the right-hand side of Eq. (5), the first and second terms correspond, respectively, to emission and reflection of radiation from the surface element.

The solution of Eq. (4) to determine the radiation heat transfer requires integration in the space and the spectrum. In this study, the spatial integration will be carried out by the discrete ordinates method. The spectral integration will be performed with the gray gas (GG), the weighted-sum-of-gray-gases (WSGG), and the cumulative wavenumber (CW) models. These three models will be compared to the line-by-line (LBL) integration, in which Eq. (4) is integrated in every spectral line. Since the LBL integration involves no approximation in the spectral integration, it can be considered the benchmark for comparison.

**Gray Gas Model **

Several modern studies, especially in three-dimensional or combined mode problems, still consider the gas to be gray, for which the absorption coefficient is independent of the wavenumber. The integration of the RTE with the gray gas model yields:

In solving the above equation, the absorption coefficient of the mixture is computed by the sum of the absorption coefficients of the gas and the soot phases:

In this study, the gray gas absorption coefficients for H_{2}O and CO_{2} are correlated by Barlow et al. (2001), while the gray absorption coefficient for the soot is calculated as suggested by Atreya and Agrawal (1998). The correlations are listed in Table 1. For H_{2}O and CO_{2}, the absorption coefficients are computed by κ* _{g} *= κ'

*, where κ'*

_{g}P_{g}*is given in Table 1,*

_{g}*P*is the partial pressure of the gas, and the index

_{g}*g*represents either H

_{2}O or CO

_{2}.

**The Weighted-Sum-of-Gray-Gases (WSGG) Model**

The integration of the RTE, Eq. (4), with the WSGG model leads to:

in which κ* _{j} *and

*a*corresponds, respectively, to the absorption coefficient and the weighting factor for the

_{j}*j*-th gray gas. Equation (8) is subjected to the following boundary condition:

where the weighting factor for the *j*-th gray gas is given by:

In the above equation, *E _{b}*

_{η}and

*E*are, respectively, the spectral and the total blackbody emissive power, computed at the medium temperature. Finally, the total intensity for

_{b}*N*gray gases can be found by summing the intensities associated with each gray gas:

The WSGG model is frequently used with the correlations proposed by Smith et al. (1982, 1987) for the mixture of gases and soot. Although these correlations have been proved to be outdated, as discussed in Galarça et al. (2008), they continue to be extensively employed in engineering analysis, and were chosen to be used in this work to illustrate how they compare to solutions with modern gas data. The correlations are listed in Table 2 for a gas mixture with a molar ratio of 2:1 between water vapor and carbon dioxide. The local absorption coefficient of the *j*-th gray gas is obtained by the product between the modeled coefficient κ'* _{g} *and the total partial pressure of water vapor and carbon dioxide,

*P*

_{CO2}+

*P*

_{H2O}. The temperature dependent weights are approximated by a cubic polynomial function, given by:

in which *b _{g,ji} *is the polynomial coefficient obtained in Table 2, where

*m*and

*n*are labels for gray gas and soot, respectively.

For a mixture with soot, one more gray gas with null absorption coefficient is added (κ_{g,0} = 0), corresponding to the transparent windows of water vapor and carbon dioxide. Its correspondent temperature dependent weight is given by:

In the case of pure gas mixtures, the transparent windows do not contribute to the process, but in a mixture of gases with soot one should consider the emission and absorption of soot in the corresponding spectral regions.

For soot, the corresponding absorption coefficient is obtained by the product of the model coefficient and the soot volumetric fraction, and its weighting is given in an analogous way to Eq. (12). Thus, the absorption coefficient used in Eq. (7) for the mixture of the gases and soot is obtained by all possible combinations of the gas and soot absorption coefficients given in Table 2, defined as:

The temperature dependent weights for the mixture are defined as:

where the dimension of *j *is *m×n*.

**The Cumulative Wavenumber Model**

In this model, the entire spectral range of the absorption crosssection is divided into several gray gases and a non-decreasing function, called the cumulative wavenumber function, *w*, which is defined as:

where *H*(*C*-*C*_{η}) is the Heaviside step-function, *C *is the absorption cross-section of the gray gas, and *C*_{η} is the absorption cross-section. Differentiation of Eq. (16) with respect to η yields:

Thus, the integration of the wavenumber only in the regions where the gray gas coefficient *C *is larger than the true absorption cross-section is equivalent to integrating the derivative of the cumulative wavenumber function in the entire spectrum, according to:

The cumulative wavenumber method, proposed by Solovjov and Webb (2002), can be thought as a discretization in the fractional gray gas wavenumbers (*D _{ij}*) space. This interval

*D*is defined as an intersection of two wavenumber intervals,

_{ij}*H*and Δ

_{j}*. The interval*

_{i}*H*is the wavenumber region where the absorption cross-section is between two adjacent gray gases, that is:

_{j}And the interval Δ* _{i} *is the wavenumber region divided in subintervals:

For a position *s *and all η ∈ Δ* _{i}*, the difference between two adjacent gray gases can be viewed as a product of two functions:

where the function *v _{ij}*(η) is the difference in the wavenumber function evaluated at a reference thermodynamic state

*s**. Thus, function

*u*(

_{ij}*s*) can be defined as:

As shown in Solovjov and Webb (2002), the integration of the radiative spectral intensity *I*_{η} over the fractional gray gases *D _{ij} *intervals, using the cumulative wavenumber approach yields:

where *J _{ij} *and

*u*are viewed as a fractional gray gas intensity and a local correction to the fractional gray gas intensity, respectively. With this approach, Eq. (4) can be written as:

_{ij}where κ* _{j} *is the gray gas absorption coefficient, defined as:

and *J _{bij} *is the fractional blackbody radiative energy source:

The total intensity is obtained by the summation of the product between *u _{ij} *and

*J*over all fractional gray gases, that is:

_{ij}In the CW method, the spectrum is assumed to vary linearly with the concentration:

It is also assumed that the intersections of the gray gases *C *with the spectrum *C*_{η} + *C*^{* }(the sum of the absorption cross-section with the absorption coefficient of gray particles) produce the same wavenumber intervals as the intersections of the gray gas *C* - *C** with the spectrum *C*_{η}, that is:

For a mixture of gases and soot, Solovjov and Webb (2002) defined some approaches that can facilitate the use of this method: the superposition approach, the multiplication approach, and the hybrid approach. In this work, it is used the superposition approach, which assumes that the absorption cross-sections of the *r *species do not overlap and that the non-gray particles are piece-wise constant in the interval Δ* _{i}*. Thus,

where *C _{i}^{s} = *κ

_{η}for η ∈ Δ

*, and κ*

_{i}_{η}is given by Eq. (3).

**Results **

In this section, it is analyzed the influence of soot in the radiative heat transfer as well as in the results of the different gas models. It is considered a one-dimensional geometry formed by parallel black walls placed at a distance of *L *= 1.0 m from each other. The position in the medium is defined by *x*, with the walls located at positions *x *= 0 and *x *= *L*. The space between the two walls is filled with a mixture of gases composed of 10% CO_{2} and 20% H_{2}O. From the ideal gas mixture theory, the ratio between the partial pressure of each species to the total pressure is equivalent to its molar concentration, thus *Y*_{CO2} = 0.1 and *Y*_{H2O} = 0.2. The medium temperature varies according to the following equation:

where 0 __<__ *x *__<__ *L *= 1.0 m, *T _{s} *= 500 K, and

*T*

_{max}= 1000 K. With the above relation, the temperature in the medium ranges from 500 K, in the vicinity of the surfaces, to 1000 K at the half distance between the surfaces, which are assumed black (ε

*= 1). Four soot volumetric fractions are considered:*

_{w}*f*= 1×10

_{v}^{-8 }, 1×10

^{-7 }, 1×10

^{-6 }and 1×10

^{-5}. The last case, with

*f*= 1×10

_{v}^{-5}, is a higher than usual concentration in combustion of hydrocarbons, but it can represent situations where soot formation is intensified to supposedly increase the radiation effect.

Results are presented for the divergence of the radiative heat flux, in units of W/m^{3}, which is one of the main parameters in the computation of radiation in participating media. It corresponds to the net rate of energy that leaves each element of volume in the medium per unit of volume, and is equivalent to the radiative heat source, but with opposite sign: *dq*_{R}*/dx *=−_{R }. When the divergence of the radiative heat flux is positive, it means that the element loses energy due to radiation. The divergence of the radiative heat flux is expected to be positive in the higher temperature regions of the medium and negative in the lower temperature regions of the medium.

Figure 2 shows the radiative heat source _{R }=− *dq*_{R}*/dx *that was obtained with line-by-line integration. In all cases, the radiative heat source was positive in the medium regions close to the surfaces, indicating that the gain of radiation from the hot regions of the medium exceeded the loss of radiation to the surfaces. Moving from the surfaces, *x *= 0 and *x *= *L, *towards the center, *x *= *L*/2, the radiative heat source decreased until it reached negative values, meaning that the loss exceeded the gain of radiation energy. Comparing the solutions for different soot volumetric fractions in Fig. 2, one can see that there is no significant difference between the case where there was no soot and the case with a very low concentration (*f _{v} *= 1×10

^{-8}). When the soot volumetric concentration was increased to

*f*= 1×10

_{v}^{-7}, a considerable increase occurred in the absolute value of the radiative heat source in the higher temperature region of the medium, indicating an increase of radiation transferred to the colder regions of the domain. On the other hand, only a small variation occurred in the colder region, indicating that the increased gain of energy from the hot regions of the medium was compensated with an increased loss of energy to the surface. Figure 2 also shows that, when the soot concentration was incremented to

*f*= 1×10

_{v}^{-6 }, there was a strong increase in the radiation exchanged. In this case, the gas had only a minor contribution to the radiative heat transfer, which was soot dominated. Finally, for the situation where the soot concentration was as high as 1×10

^{-5 }, the absolute value of the radiative heat source decreased in the center of the medium. In this situation, the medium became so optically thick that caused a decrease in the amount of radiation exchanged in the system. This behavior will be further explored later in this section.

Results for the radiative heat source obtained with the GG, WSGG and CW models for the case with no soot, *f _{v} *= 0, are presented in Fig. 3. As can be observed, the GG model presents results with considerably large deviations from the LBL solution, leading to an overestimation of the radiation exchange in the system. The WSGG model presents results with a smaller but still noteworthy deviation from the LBL solution, which can be attributed to the fact that the correlations provided in Smith et al. (1982) were based on old gas data, which are known to be inaccurate. Finally, the CW model led to results that compared well with the LBL solution, with exception of the medium region close to the surfaces. It should be noted that the CW solution was built with the same spectral data of the LBL integration, and the model itself is based on a more sophisticated spectral analysis than the simpler approaches of the GG and the WSGG solutions. Additional comparison between the models can be made with the analysis of their relative errors, Δ, which was computed in this work as:

where max(_{R,LBL}) is the maximum value for the radiative heat source for each volumetric fraction of soot.

Results for the maximum and average values of the relative error, Δ_{max} and Δ_{avg}, are presented in Table 3 for all cases discussed in this study. The table indicates the high values of the relative errors for the GG and WSGG solutions, with maximum errors of 225.5% and 55.6%, respectively, for no soot. The CW model also led to a large maximum error, Δ_{max} = 29.5%, but the average error, Δ_{avg} = 7.6%, indicates that the model can be sufficiently accurate to compute the radiation exchange for engineering computations when soot is not present.

Figures 4 to 7 compares the solutions from the GG, WSGG and CW models with the LBL integration where the medium contains different amounts of soot. For small concentration of soot (*f _{v} *= 10

^{-8 }, seen in Fig. 4), the general trends of the solution remained the same of the case without soot, but in general the deviation of the solutions to the LBL integration decreased, as can be observed in Table 3. By increasing the volumetric fraction of soot to

*f*= 10

_{v}^{-7}, as shown in Fig. 5, the deviation of the GG and WSGG models to the LBL solution continued to decrease, especially for the GG model. As for the CW solution, although the maximum and average deviations did not change considerably from the previous cases (

*f*= 0 and

_{v}*f*= 10

_{v}^{-8}), the point of maximum deviation moved from the region close to the surface to the center of the domain. Results for the highest amounts of soot,

*f*= 10

_{v}^{-6 }and

*f*= 10

_{v}^{-5}, are presented in Figs. 6 and 7, with major modifications in previous trends. First, results with the GG model became considerably more accurate in comparison to the LBL solution, in special for

*f*= 10

_{v}^{-5}, where the maximum and average errors decreased to Δ

_{max}= 14.4% and Δ

_{avg}= 7.9%, respectively. On the other hand, the CW model led to considerably large deviations, Δ

_{max}= 297.7% and Δ

_{avg}= 151.7%. This change in the trend can be attributed to soot radiation being dominant for

*f*= 10

_{v}^{-5}. While the GG model allows a straightforward approach to include soot in the integration of the radiative transfer equation, the CW model, proposed to deal with the highly complex dependence of the radiative properties of participating gases, requires a more elaborate approach that can fail when radiation is dominated by soot. Though not as critical as with the CW model, the WSGG model led to large errors when the amount of soot was increased.

Although it is expected that some of the above results depend on the thermal conditions and concentrations of the chemical species, it is possible to draw some practical conclusions regarding the use of the different models to compute radiation heat transfer in media containing participating gas and soot. Firstly, some of the available correlations to use the GG and the WSGG models must be carefully used, since they may be obtained from old, inaccurate gas data. In addition, these models are based on assumptions that cannot represent a variety of physical conditions. However, these simple models allow a more straightforward inclusion of soot than modern gas models such as the CW model, and can lead to reasonably satisfactory results when soot radiation dominates the process. One challenge that follows from this is to compute heat transfer in systems in which the concentration of soot varies locally. In this case, one possible approach, still not attempted so far, would be the use of different gas models with dependence on the amount of soot.

One final discussion concerns the observation that the increase of soot from *f _{v} *= 0 to

*f*= 10

_{v}^{-6}led to an increase in the overall radiation heat transfer, but for an even higher concentration of soot,

*f*= 10

_{v}^{-5}, an opposite effect was observed, that is, the decrease in the radiation transferred from the medium to the surfaces. For a more complete understanding of the phenomenon, Fig. 8 presents the radiative heat source in the mid-point between the two surfaces (

*x*/

*L*= 0.5) for different values of the optical thickness, τ = κ

*L*. As seen, for τ &8594; 0, the radiative heat source tends to zero, as expected for the limit of non-participating media. For τ &8594; &8734;, in the limit of very thick media, the radiative heat source also tends to zero, since the media is so thick that radiation hardly escapes the point of emission. Figure 8 shows that the maximum absolute value of the radiative heat source occurs for τ ≅ 3.0. Considering the radiation properties determined from the gray gas model, the optical thicknesses based on the average absorption coefficient were τ ≅ 5.5 and τ ≅ 15.4 for the cases with

*f*= 0 and

_{v}*f*= 10

_{v}^{-5}, respectively, explaining the decrease in the radiation exchange between the first and later cases. Thus, intensifying the formation of soot to increase radiation heat transfer can be beneficial only up to a certain point.

**Conclusions **

This study considered the solution of the radiation heat transfer in a medium composed of soot and participating gases (water vapor and carbon dioxide). The radiative heat transfer equation was integrated with the use of three gas models, the gray gas (GG), the weightedsum-of-gray-gas (WSGG) and the cumulative wavenumber (CW) models. The results of the three models were compared with the lineby-line (LBL) integration, which can be considered a benchmark solution. The GG and WSGG models were based on correlations that are widely employed in engineering analysis of radiation heat transfer, and led to results that shown considerable deviation from the LBL solution when the medium was composed solely of water vapor and soot. The inclusion of soot led to an improvement of the solutions provided by these two models, especially when radiation was dominated by soot. The CW model was built with the same spectral data of the LBL, leading to a satisfactory comparison for the medium composed solely of water vapor and soot, but led to large deviations when radiation was dominated by soot. The results presented show, therefore, that the choice of the gas model should take into account the amount of soot. More importantly, they reveal the need to develop new models or approaches to attempt a general treatment of the radiation heat transfer in media composed of constituents that present different spectral behavior, such as participating gases and soot.

**Acknowledgements **

The authors thank CAPES (Brazil) for the support under the Program CAPES/UT-AUSTIN, No. 28/2008. FHRF and HAV also thank CNPq for research grants 304535/2007-9 and 302503/2009-9, respectively, and for CNPq Universal Project 475237/2009-9.

The four last authors of this paper express their utmost gratitude for the opportunity to work with Anderson Mossi, who passed away a few weeks prior to his doctorate defense, in April of 2011. Anderson Mossi was a highly talented young researcher, who gained several friends in Brazil and USA with his great sense of humor and very positive attitude towards life. He is very much missed by all of us.

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Paper received 31 October 2011.

Paper accepted 10 January 2012

**Technical Editor: Fernando Rochinha**