MODELING CHAR OXIDATION AS A FUNCTION OF PRESSURE ...

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8. Summary and Conclusions The objective of this project was to develop a model that can be used to explain and unify char oxidation rates over wide ranges of experimental conditions, including temperature, total pressure, oxygen mole fraction and particle size. A secondary objective of this work was to explore how the apparent reaction order of char oxidation changes with experimental conditions. The theoretical challenge in carbonaceous solid combustion, known as the rough sphere combustion phenomenon, was also explored. The accomplishments are summarized and conclusions are drawn below. Analytical Solutions of the Effectiveness Factors Bischoff (1965) proposed a so-called “general asymptotic solution” for predicting the effectiveness factor for an arbitrary rate form. Based on the work of Bischoff, a general modulus (Eq. 2.30) was obtained in this study for the Langmuir rate equation. This is the first time that the general modulus for the Langmuir rate equation has been applied to char oxidation. The asymptotic solutions of the effectiveness factors for both the Langmuir rate equation and the m-th order rate equation were examined by comparison with numerical solutions. It was found that the general asymptotic solutions lead to errors as high as 17% in the intermediate range of the Thiele modulus. A correction function was developed to improve the accuracy of the general asymptotic solutions. The corrected 121
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MODELING CHAR OXIDATION AS A FUNCTI
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BRIGHAM YOUNG UNIVERSITY As chair o
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CBK model uses: 1) an intrinsic Lan
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Table of Contents List of Figures..
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Appendices.........................
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Figure A.2. Mass releases of the Ko
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Table 7.6. Parameters Used in Model
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Ed activation energy of desorption,
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vc the volume of combustible materi
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Background 1. Introduction The rate
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the CBK model developed at Brown Un
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Zone III rate ∝ C og E obs → 0
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coal-general kinetic rate constants
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Boundary Layer Diffusion The molar
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= q obs q max The factor can be use
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where k 1 and K are two kinetic par
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particle can therefore be convenien
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This is the first time that the gen
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Data of Mathias Mathias (1996) perf
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urn with shrinking diameters, and t
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3. Objectives and Approach The obje
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Introduction 4. Analytical Solution
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Task and Methodology Task One of th
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2 [ (i +1) − (i − 1)] i b = −
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Table 4.1. The Relative Error * (%)
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The resulting observations regardin
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correction. The values of functions
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Table 4.6. The Relative Error* (%)
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Table 4.8. The Relative Error* (%)
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general asymptotic solution. An arc
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5. Theoretical Developments The int
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order of a reaction is usually dete
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nobs = 1 (KCs ) 2 2 1 [KCs − ln(1
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The observed reaction order in Zone
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Bulk Diffusion vs. Knudsen Diffusio
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where D K is in cm 2 /sec, r p is t
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where T p is in K, P is in atm. The
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Both of these assumptions are argua
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2 r obs ′ − [kD Pog + k d + kD
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oxygen partial pressure (Suuberg et
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Farrauto and Batholomew (1997) prop
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assumes a homogeneous, non-interact
Page 90 and 91: Single-Film Char Oxidation Submodel
Page 92 and 93: where and An energy balance is used
Page 94 and 95: where is the empirical burning mode
Page 96 and 97: calculation uses a 7 × 7 × 7 matr
Page 98 and 99: HP-CBK Model Development The HP-CBK
Page 100 and 101: Effective Diffusivity The major obs
Page 102 and 103: where r p1 and r p2 are the average
Page 104 and 105: where r p1 is the macro-pore radius
Page 107 and 108: 7. Model Evaluation and Discussion
Page 109 and 110: experiments are non-porous, the rat
Page 111 and 112: and 2850 K). For consistency with t
Page 113 and 114: The value of the roughness factor w
Page 115 and 116: = S int S ext D e r p a 2 2M C M O2
Page 117 and 118: Reactor Head Flow Straightener Reac
Page 119 and 120: the large size of the particle, and
Page 121 and 122: taking into account convection, rad
Page 123 and 124: 2.5x10 -4 2 /sec) 2.0 1.5 Rate (g/c
Page 125 and 126: Table 7.5. The Experimental Conditi
Page 127 and 128: The burnout and particle velocity d
Page 129 and 130: The HP-CBK was used to predict the
Page 131 and 132: TGA and FFB Data-This Study The rea
Page 133 and 134: This equation can be derived as fol
Page 135 and 136: q = A 1p e − E 1 p / RT P os 1 +
Page 137 and 138: m obs = 0 at high temperatures) and
Page 139: Currently the correlations between
Page 143 and 144: 0.5 due to the contribution from th
Page 145 and 146: Langmuir rate equation, the reactio
Page 147 and 148: II, in agreement with many observat
Page 149 and 150: 9. Recommendations The predictive c
Page 151 and 152: References Ahmed, S., M. H. Back an
Page 153 and 154: Essenhigh, R. H., D. Fortsch and H.
Page 155 and 156: Mehta, B. N. and R. Aris , “Commu
Page 157 and 158: Szekely, J. and M. Propster, "A Str
Page 159 and 160: Appendices 139
Page 161 and 162: Introduction Appendix A: Experiment
Page 163 and 164: detaching the flame from the burner
Page 165 and 166: To study the effects of steam, CO w
Page 167 and 168: times at heights of 1, 2, 4, and 6
Page 169 and 170: analysis. The char reactivities (in
Page 171 and 172: Table A.5. Moisture, Ash and ICP Ma
Page 173 and 174: Table A.9. Elemental Analyses of Fo
Page 175 and 176: temperature profile of the post-fla
Page 177 and 178: Apparent densities 1.00 0.75 0.50 0
Page 179 and 180: This observation is somewhat surpri
Page 181 and 182: It is interesting to compare Figure
Page 183 and 184: The N 2 BET surfacea areas and H/C
Page 185 and 186: collected in the #4 reactor conditi
Page 187 and 188: Rate (gC /g C remaining /sec) 1.6x1
Page 189 and 190: close to zero, the accumulated erro
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Appendix B: Errors and Standard Dev
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