Abstract
Gasification has been one of the most attractive and common biomass conversion processes for recent years. The existence of an accurate and dynamic model frees us from carrying out time-consuming and expensive tests. In this study, to eliminate the complexity of dynamic models, a hybrid model is used for modeling the process of wood-fixed bed gasification. Firstly, an equilibrium model is developed to obtain the mole fractions of product flow and the equilibrium temperature of the flaming pyrolysis zone. The equilibrium model is applied as the initial condition of the unsteady one-dimensional kinetic model for the reduction zone. The couple of heat and mass equations in the gas phase are solved by considering the kinetic of main reactions in the reduction zone using MATLAB software. Oxygen is considered gasifying agent instead of air. The results indicate a good agreement with previous relevant researches. In the equivalence ratio of 0.35, the maximum mole fraction of hydrogen as the most valuable syngas has obtained. In this optimum ER, the equilibrium temperature of flaming pyrolysis zone has been calculated to be 1012 K, and the gasifier outlet temperature at gas-phase velocity within 0.1–1 m/s is 890–952 K. The final mole fractions of CO and H2 as the main products of the process are 0.46 and 0.36, respectively. The heating value of produced syngas equals 10.8 MJ/m3 that is 120% higher than the average heating value when the air is utilized as the gasifier agent.
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Abbreviations
- A :
-
Pre-exponential factor
- a :
-
Number of moles of oxygen per mole of biomass
- Ash:
-
Ash content of dry biomass
- C :
-
Molar concentration (mol/m3)
- C p :
-
Molar-specific heats (J/mol K)
- D i :
-
Diffusion coefficient (m2)
- d p :
-
Particle diameter (m)
- E :
-
Activation energy (kJ)
- ER:
-
Equivalence ratio
- FC:
-
Activation energy
- MC:
-
Moisture content in the fuel in mass percentage
- g ° :
-
Gibbs function (J/mol)
- \( {{\overline{h}}_{\mathrm{f}}}^0 \) :
-
Enthalpy of formation (kJ/mol)
- HHV:
-
Higher heating value (MJ/kg)
- k :
-
Equilibrium constant
- k m :
-
Mass transfer coefficient (m/s)
- k ∗ m :
-
Maximum value of the mass transfer coefficient (m/s)
- M:
-
Molecular weight (g/mol)
- P :
-
Gas pressure (kPa)
- Q loss :
-
Heat loss (kJ)
- r :
-
Specific reaction rate (mol/(m3 s))
- R :
-
Universal gas constant (J/(mol K)
- Re :
-
Particle Reynolds number
- Sc:
-
Particle Schmidt number
- T :
-
Temperature (K)
- t :
-
Time (s)
- U g :
-
Gas-phase velocity (m/s)
- w :
-
Number of moles of moisture for per mole of biomass
- x :
-
Number of moles
- Y :
-
Mole fraction
- z :
-
Distance (m)
- ε :
-
Porosity
- ν p :
-
Particle density number (1/m)
- ρ g :
-
Gas-phase density (kg/m3)
- λ g :
-
Gas-phase thermal conductivity (J/(mol K))
- ΔH :
-
Reaction enthalpy (kJ/mol)
- α :
-
Stoichiometric coefficient
- 0:
-
Initial or ambient condition
- a :
-
Air
- in:
-
Inlet
- i :
-
Species
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Fani, M., Haddadzadeh Niri, M. & Joda, F. A Simplified Dynamic Thermokinetic-Based Model of Wood Gasification Process. Process Integr Optim Sustain 2, 269–279 (2018). https://doi.org/10.1007/s41660-018-0042-5
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DOI: https://doi.org/10.1007/s41660-018-0042-5