1. Introduction
Biomass is characterized by its diversity, abundance, and renewability. It is accordingly considered one of the most important sources of renewable energy [
1]. It is an important renewable energy source as it helps with the increasing energy utilization in addition to satisfying the requirements of sustainable development with near zero CO
2 emissions [
2,
3]. Biomass gasification has gained worldwide attention thanks to its high energy conversion efficiency as well as its ability to operate with important ranges of biomass feedstocks. It is a thermo-chemical process that uses heat, involving pyrolysis, combustion, and reduction, to convert biomass into producer gas/synthesis gas (syngas) through a series of heterogeneous and homogeneous reactions. Synthesis gas usually contains H
2, CO, CH
4, N
2, and other undesirable components such as CO
2 and tar, and can be used for different purposes: generation of other valuable products for the chemical industry as well as power and heat [
4].
Several factors can affect the composition of product gas and the concentration of its impurities [
5], such as the reactor design, the gasifying agent and its velocity, the temperature of the reactor, etc. In fact, biomass gasification can occur in typical single stage reactors or in multistage ones. Depending on the gas velocity, gasification can take place in different regimes, for instance, fixed bed, bubbling bed, and circulating bed. Loha et al. [
6] stated that fluidized beds are preferred for the gasification of biomass as they promote the solid feedstock conversion by an excellent mixing and contact between gas and solid particles. In addition, integrating char in the fluidized bed can be used as an effective means for tar decomposition, as stated by Basu [
4]. There are many researchers [
7,
8,
9] who investigated the effect of multistage gasification systems and they affirmed that they upgraded the quality of the product gas by diminishing the tar concentration. Therefore, an exclusive gasification technology, a multistage fluidized bed gasifier, that aims at low tar production could be developed on the basis of the above-mentioned principles.
Several researchers have focused on modeling biomass gasification using the Aspen Plus simulator in order to study and determine the optimal composition of the produced gas. In addition, the development of gasification reactors generally needs different levels of material and human resources. Therefore, using computer simulations is the efficient way to solve this problem. The Aspen Plus simulator is a program process that can be used to compute mass and energy balances dealing with multiphase models. It is used in the simulation of a diversity of processes like fluidized-beds and gasification reactors [
10]. The performance analysis of fluidized beds for biomass gasification can be studied using thermodynamic equilibrium or kinetic modeling [
11]. Two different thermodynamic models employing Gibbs energy minimization have been used by different researchers [
11]. Thermodynamic equilibrium models do not consider the hydrodynamics of the process. They are independent of the gasifier type, unlike thermodynamic semi-equilibrium models which provide better prediction of producer gas composition. The kinetic models take into consideration both the hydrodynamic behavior and the reaction kinetics to make it the physically most realistic model. Mallick et al. [
11] stated that this approach is very important when it comes to designing, improving, and evaluating gasification systems. Most of the studies did not consider tar, or loaded it over other heavy hydrocarbons [
12]. Some others considered it as chemically inert, so it did not take part in the chemical reactions [
13]. Regarding pyrolysis, some researchers [
6] considered it as an instantaneous process. According to this assumption, the pyrolysis compositions can be used as inputs in gasification simulations.
Niu et al. [
14] focused on a comprehensive modeling using Aspen Plus to simulate the solid waste gasification inside a fluidized bed gasifier. They stated that the production of CO and H
2, and the gasification efficiency were improved as a result of the increase of gasification temperature. Doherty et al. [
15] used the Aspen Plus simulator to study a fluidized bed process. Their model was also based on Gibbs free energy minimization. They found that syngas composition and heating value were strongly influenced by both gasification temperature and steam to biomass ratio. In addition, it was stated that cold gas efficiency was affected by the biomass moisture. Likewise, on the basis of Gibbs free energy minimization, Sreejith et al. [
16] developed a steam gasification biomass model using the Aspen Plus simulator. Their study was based on an equilibrium model based on Gibbs free energy minimization and aimed to determine the optimum process conditions of gasification. Using the same model, Begum et al. [
3] developed an Aspen Plus model to study different biomass feedstocks’ gasification. It is about a fixed bed integrated gasifier that predicted the model’s steady state performances. The authors could provide the optimum performance for the feedstocks studied. Mitta et al. [
17] presented a model for a fluidized bed type gasification process. Their study focused on the effect of the flow rate, the temperature and composition of the feed material, and the operating pressure and temperature. The developed model was able to predict the composition of the produced gas and the effect of operating temperature on the gas composition.
Beheshti et al. [
18] simulated the air–steam biomass gasification to produce hydrogen and syngas. They used an Aspen Plus model based on chemical reaction rates and hydrodynamic properties: a semi detailed kinetic model. Empirical correlations of pyrolysis yields were used. They studied and discussed the effects of some critical parameters like gasification temperature, biomass particle size, steam to biomass ratio, and equivalence ratio on the composition of the gas produced. Abdelouehed et al. [
19] studied biomass gasification in dual fluidized beds. They modeled the process by Aspen Plus using a semi detailed kinetic mechanism. In their work, pyrolysis products were calculated through correlations and were considered as feeds to other reactors. Their model predictions for methane and tar yields were in agreement with data of pilot plants. They stated that the semi detailed kinetic model can be used to optimize biomass gasifier performances.
The present work focuses on gasification modelling using a semi detailed kinetic model in the Aspen Plus Simulator. The innovation points of the multistage gasifier studied are the design and the usage of a fluidized bed in the reduction zone to produce a high-quality product gas. This reactor has been studied in CFD cold model. The novelty of this study is to develop a numerical tool that introduces species and chemical reactions in order to investigate the main product gas composition, lower heating value (LHV), and cold gas efficiency (CGE), depending on the variation of gasification temperature and bed material. The hydrodynamics of the bed were investigated as well.
3. Validation
Due to a lack of experimental data for
Prosopis juliflora gasification in fluidized bed, the feedstock used to validate the model is wood pellets (CH
1.4O
0.64)
33 which is used by Campoy et al. [
30]. A comparison with their experimental data from air–steam gasification of wood pellets in a bubbling fluidized bed reactor is analyzed. A comparison with numerical data of Beheshti et al.’s [
18] Aspen Plus model is made as well. Correlations are used for predicting devolatilization products.
Campoy et al. [
30] used wood pellets as fuel and ofite, which is a silicate subvolcanic rock with formula (Ca, Mg, Fe, Ti, Al)
2(SiAl)
2O that has a density of 2650 kg/m
3, as bed material. They considered air and air with steam as gasification agents. The stoichiometric ratio (SR) and steam to biomass ratio (SBR) ranged from 0.19 to 0.35 and from 0 to 0.45, respectively, by changing both the vapor flow rate (from 0 to 5.1 kg/h) and the biomass flow rate (from 12.2 to 20.5 kg/h) while retaining an approximately steady air flow rate (from 17 Nm
3/h). The operating temperature ranged between 730 °C and 815 °C.
Table 3 describes the pilot plant’s most critical parameters, under the terms of the research experiments. Details of the gasifier plant and different input parameters can be found in their work [
30].
Table 4 displays the LHV of the syngas in addition to its composition. It is shows that the model results are in good agreement with Campoy et al. [
30] and Beheshti et al.’s [
18] findings. More specifically, the present model presents syngas composition’s percentages close to the existed data. Percentages were closer to the experimental ones [
30] than those of Beheshti et al.’s [
18] values. The LHV calculated by the present model was found to be 6.699 MJ/Nm
3 and showed a good agreement with the experimental value as well, which was found to be 4.76 MJ/Nm
3.
4. Results and Discussions
The volume of the combustion reactor is set at V
comb = 0.3 m
3, while the diameter of gasification reactor changes from 0.35 m to 0.55 m. The maximum height of the gasifier is between 2 m and 4 m. The biomass
Prosipis juliflora mass flow is 10 kg/h. With respect to Chandrasekaran analysis [
21], this mass flow gives 6.64 kg/h (char + gas) which represents 66.4% of pyrolysis product of PJ. Char represents approximately 21% and gas represents 45.4% of fuel mass flow. Subsequently, 2.1 kg/h of solid char is assumed to enter the gasifier reactor. A 4.54 kg/h of pyrolytic gas is considered as an input of the combustor reactor considered isothermal at 1000 °C and maintained at 1 bar. The corresponding mass flow of the air varies between 2 and 5 kg/h at 25 °C and is mixed with pyrolytic gas at 600 °C.
In the following, a parametric study of the effect of gasification temperature, air to biomass ratio, and gasifier dimensions (diameter and height) is presented. The composition of syngas and its LHV along with cold gas efficiency (CGE) are the principal studied output variables. In addition, flow regimes in the fluidized gasifier are identified for different bed inventories.
4.1. Effect of Gasifier Temperature
The considered parameters are: air/biomass ratio = 40%, gasifier diameter D = 0.5 m, and gasifier height H = 2.5 m.
4.1.1. Syngas Composition
According to
Figure 2a, the CO molar fraction is prevailing and clearly increases with T
gasif; however, CO
2 concentration decreases. As a consequence, the LHV of syngas also increases with T
gasif (
Figure 2b). This rising tendency is already mentioned in previous studies for biomass air gasification [
7], CO
2 gasification [
31], and steam gasification [
32] for low steam to biomass ratio.
Figure 2a reveals that the production of gases with lower molecular weights is favored by any rise in gasification temperature. Additionally it must be mentioned that the thermodynamic equilibrium model predicts much greater conversion for the Boudouard reaction, causing considerably higher carbon monoxide concentrations and consistently lower carbon dioxide values [
31].
No considerable increase in CO concentration is observed for T
gasif greater than 900 °C. The absence of steam in the gasifier may be noted. Supplementary simulations with injection of steam inside the gasifier (easily to introduce in “fluidbed” block) show that H
2 molar fraction increases with T
gasif; however, the concentration of CH
4 decreases. This behavior is well confirmed in the literature [
28]. Recently Lan et al. [
33] presented a comparison between fluidized bed biomass gasification with and without steam. With the addition of steam and as the bed temperature increased, gas reforming reactions rose, and the CO and CH4 content diminished; however, CO
2 and H
2 content went up.
4.1.2. LHV and CGE
The increasing tendency in
Figure 2b is directly related to producer gas composition for different gasifier temperatures (
Figure 2a).
Figure 2b shows that T
gasif = 900 °C gives a satisfactory LHV of syngas (11.43 MJ/Nm
3) and maximal cold gas efficiency CGE (63%) of the entire gasifier. This promising LHV value is relatively high for air biomass gasification even for low air/biomass ratio.
4.2. Effect of Air/Biomass Ratio
The considered parameters are: Tgazif = 900 °C, gasifier diameter D = 0.5 m, and gasifier height H = 2.5 m.
4.2.1. Syngas Composition
Figure 3a shows a remarkable N
2 rate increase for higher air/biomass ratios. As predicted a rise in CO
2 molar fraction and a reduction in CO fraction are observed.
4.2.2. LHV and CGE
Figure 3b shows a decreasing trend of LHV when air/biomass ratio increases. The principal reason for this behavior is the combustion reactions happening in the combustor for a greater air flow rate. This is confirmed in
Figure 4 showing gas composition at the output of the combustor. For air mass rate near 5kg/h, all CO is oxidized leading to an increase in CO
2 fraction. H
2O is also completely consumed due to the favored water gas shift direct reaction (R5) at high temperature.
According to
Figure 3b, the maximum of CGE (63.7%) is obtained for the equivalence ratio of 0.4 (i.e., air mass flow equal to 4 kg/h). The corresponding LHV value is 10.5 MJ/Nm
3. Indeed, despite the diminishing of LHV with rising air/biomass ratio, the CGE would first increase owing to the growing volume of carbon transformed into gaseous products and then decline due to the dominant effect of the N
2 dilution of the producer gas. With the increase of air/biomass ratio, the quantity of the oxygen brought to the combustion reactor increases. The gas components of pyrolytic gas burn inside the combustor in the situation of oxygen enrichment and the content of combustible gas is reduced. Accordingly, the temperature increases in the combustion reactor. Nevertheless, the rise in temperature is advantageous to the gasification reactions occurring inside the gasifier. Alternatively, the biomass gas concentration is diluted significantly. Consequently, the increase of air/biomass ratio has a mutual effect on the rise and decline of the combustible gas content in the producer gas. Nevertheless, this analysis is not totally adequate for isothermal combustion and gasification reactors.
To analyze and evaluate this rate of 4 kg/h of air mass flow, one can focus on the combustor reactor and calculate the corresponding equivalence ratio ER
comb. According to equations R1-R7, one mole of the pyrolytic gas (PYRGAS) consumes 0.6225 mole of O
2 in stochiometric combustion. Considering a rate of 21% of oxygen in the air, one gets 3.635 kg (air)/kg (pyrolytic-gas) as stochiometric ratio. Having 4/4.54 = 0.881 kg (air)/kg (pyrolytic-gas) as real ratio, one gets the equivalence ratio: ER
comb = 0.24 which is inside the literature suggested interval [
4]. It is to be noted that the global equivalence ratio corresponding to the combustion of 10 kg of
Proposis juliflora (CH
0.138O
0.978N
0.043 [
21]) with 4 kg/h of air mass flow is equal to 0.13. However, this ratio is not so significant because almost zero oxygen reaches the gasification reactor and so no oxidation of char is predicted.
4.3. Effect of Gasifier Diameter
The fixed parameters are: mass flow air/biomass ratio = 40%, gasifier temperature T
gazif = 900 °C, and gasifier height H = 2.5 m.
Figure 5a shows a promising effect of increasing gasifier diameter on gas composition. In fact, for a larger diameter, the height of bottom zone is lower and the freeboard height is bigger. In addition, the minimum fluidization velocity decreases. All these changes in flow regimes favor gasification reactions.
This is confirmed in
Figure 5b where the rise in the LHV of syngas is significant between 0.35 m and 0.45 m.
Figure 5b shows an analogous behavior of CGE. It may be noted that a maximum value of the cold gas efficiency is about 63.1% for D = 0.49 m. Consequently, the diameter of 0.5 m is proposed for this multistage gasifier.
4.4. Effect of Gasifier Height
The considered parameters are: Tgazif = 900 °C, gasifier diameter D = 0.5 m, and mass flow air to biomass ratio equals 40%.
From
Figure 6 the height of 2.5 m of the gasifier is adequate for the choice of a good quality of syngas and consequently for LHV and CGE. From 2.5 m to 4 m no considerable variation is observed. This behavior is linked to the flow regime in the gasifier as discussed in the following section. It may be noted that the performance area rate is still the same for all values of H.
4.5. Flow Regimes in the Gasifier—Effect of Bed Inventory
In order to recognize different flow regimes inside the gasifier, three initial bed masses of 50, 100, and 150 kg are considered.
Table 5 summarizes parameters and results for three different bed masses of char (carbon solid). For 100 kg and 150 kg inventory, the bottom bed has a bubbling fluidized nature and the freeboard is a supplementary dilute zone. In the case of a 50 kg bed mass, there is almost 0 m of bubbling bed height.
Figure 7a, showing distribution of solid volume fraction, confirms these results. In addition, the distributions of pressure and superficial velocity in the gasifier confirm these bubbling or totally fluidized bed behaviors (
Figure 7b,c). Regarding the superficial velocity displayed in
Figure 7c, there is no significant difference between the three beds’ inventories, due to the fact that the same air mass flow was introduced in all three cases. It can be observed that the superficial velocity increased with the increase of the gasifier height which is related to the formation of bubbles in the bed, causing solid particles detachment. It increases more in the freeboard zone. A slight difference can be observed in the freeboard region between the superficial velocities of the three beds’ inventories.
A close depiction of
Figure 8 shows an increase in CO molar fraction and a decrease in CO
2 molar fraction inside the gasifier. The same behavior is observed by Cheng et al. [
24]. A linear variation of gas component fraction in the bottom zone is observed. In the splash region a constant behavior is observed and particularly no variation on CO and CO
2 molar fractions in the height between 1.2 to 1.5 m. This is closely linked to the constant behavior of superficial velocity in this region (
Figure 8c).