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Article

Energy Crops and Methane: Process Optimization of Ca(OH)2 Assisted Thermal Pretreatment and Modeling of Methane Production

1
Department of Agricultural Machinery and Technology Engineering, Faculty of Agriculture, Akdeniz University, Antalya 07058, Turkey
2
Department of Environmental Engineering, Engineering Faculty, Akdeniz University, Antalya 07058, Turkey
*
Author to whom correspondence should be addressed.
Molecules 2022, 27(20), 6891; https://doi.org/10.3390/molecules27206891
Submission received: 10 August 2022 / Revised: 30 September 2022 / Accepted: 10 October 2022 / Published: 14 October 2022
(This article belongs to the Special Issue Efficient Technology for the Pretreatment of Biomass III)

Abstract

:
Switchgrass earned its place globally as a significant energy crop by possessing essential properties such as being able to control erosion, low cost of production, biomass richness, and appeal for biofuel production. In this study, the impact of a Ca(OH)2-assisted thermal pretreatment process on the switchgrass variety Shawnee for methane fuel production was investigated. The Ca(OH)2-assisted thermal pretreatment process was optimized to enhance the methane production potential of switchgrass. Solid loading (3–7%), Ca(OH)2 concentration (0–2%), reaction temperature (50–100 °C), and reaction time (6–16 h) were selected as independent variables for the optimization. Methane production was obtained as 248.7 mL CH4 gVS−1 under the optimized pretreatment conditions. Specifically, a reaction temperature of 100 °C, a reaction time of 6 h, 0% Ca(OH)2, and 3% solid loading. Compared to raw switchgrass, methane production was enhanced by 14.5%. Additionally, the changes in surface properties and bond structure, along with the kinetic parameters from first order, cone, reaction curve, and modified Gompertz modeling revealed the importance of optimization.

Graphical Abstract

1. Introduction

Electrified transportation is expected to increase in the future; however, implementing its use will not happen everywhere, in every industry, and all at once [1]. Therefore, it is predicted that liquid biofuels will be extremely necessary for the ensuing decades. Sustainable and renewable fuel technologies have been focused on lignocellulosic energy crops as a promising substrate for producing biofuels. Due to enormously increased energy security demands coupled with climate change mitigation, the world’s biofuel production has also drastically expanded.
Energy crops, as a specific crop species, have been grown for advanced cellulosic biofuel production in recent decades. Switchgrass, one of these promising energy crops, belongs to the Poaceae family and is a native North American prairie grass species that can rapidly grow large amounts of carbohydrate-rich biomass. It is a species of C4-type plants (which utilize the Hatch–Slack cycle for carbon fixation), and as such, it can perform this process four times more productively than C3-type plants (which utilize the C3 pathway for carbon fixation). From an environmental point of view, switchgrass-based biofuels are carbon negative due to switchgrass’s high carbon sequestration ability owing to its deep and complex root system. Moreover, switchgrass has the ability to clean soils and waters by removing excess nutrients (N, P) originating from fertilization. This plant is also a great growth and living habitat for wildfowl and mammals, especially in ecotone zones between forest and agricultural fields [2,3]. From the agricultural perspective, switchgrass is very easy to establish and maintain due to its low nutrient and water requirements, high adaptability to many climates, and high resistance to naturally occurring pests and diseases [4]. Moreover, other advantages include expansion of the local market, new sources of income for the agricultural sector, diversification of feedstock sources, more effective resource utilization, innovation in industrial and agricultural technology, and economic growth [5]. The only drawback of switchgrass related to biofuel production bioprocessing is its lignocellulosic structure, which is highly resistant to hydrolysis [6].
Hydrolysis is the rate-limiting step for the anaerobic digestion (AD) process, even for less complex substrates than lignocellulosic biomass. Therefore, to utilize lignocellulosic biomass in AD efficiently, a pretreatment process needs to be applied. Pretreatment makes the crystalline, compact, and solid structures of lignocellulose suitable for chemical and biochemical conversion. A wide range of pretreatment processes, such as physical, chemical, thermal, and biological, and their combination has been investigated for lignocellulosic biomass in the literature for the last few years [7]. The objective of chemical pretreatment using chemicals is to break down the structure to open up cellulose and hemicellulose and remove lignin. Alkaline pretreatment efficiently removes the hemicellulose and lignin content by attacking the ether and ester bonds in lignocellulose [8]. The mechanism behind the alkaline pretreatment is explained to be the solvation and saponification of intermolecular ester bonds cross-linking xylan, lignin, and other hemicelluloses. The solvation and saponification eliminate these cross-links and enhance the porosity of the lignocellulosic materials [9]. The main advantage of alkaline pretreatment is the delignification [10]. Alkaline pretreatment depends on feedstock type, applied dose, and the pretreatment conditions [6]. CaO and Ca(OH)2 pretreatment is the most widely preferred among the various alkaline chemicals (sodium, potassium, calcium, and ammonium hydroxides) for enhancing the hydrolysis of various lignocellulosic biomasses [11,12,13,14] since it is less expensive and safer.
The AD of switchgrass, considering the methane yield for various harvesting seasons [15,16,17,18], co-digestion [19,20,21], AD kinetic modeling [22,23,24,25], and continuous AD with process performance [26,27,28,29], has been investigated in the literature. On the other hand, relatively limited research has been conducted on the pretreatment process to increase methane production from switchgrass [3,4,24,25,27,30,31,32]. Chemical-assisted thermal pretreatment application enhanced methane production in the range of 5–326% compared to raw switchgrass. Additionally, only three works in the literature [3,4,30] optimized the pretreatment of switchgrass and evaluated the process variables in detail to enhance methane production.
Since switchgrass is a complex substrate as lignocellulosic material, it needs pretreatment to break down the structure, open up cellulose and hemicellulose, and remove lignin to produce biogas. Therefore, this study aims to optimize the Ca(OH)2-assisted thermal pretreatment process to enhance methane production from the switchgrass variety, Shawnee. Central composite design (CCD) of response surface methodology (RSM) was selected for the optimization procedure. Solid loading as DM (3–7%), Ca(OH)2 concentration (0–2%), reaction temperature (50–100 °C), and reaction time (6–16 h) were chosen as independent variables. The effects of these independent variables on pH, sSugar, and methane production were investigated, and the Ca(OH)2-assisted thermal pretreatment process was modeled and optimized for maximum methane yield. The impact of the Ca(OH)2-assisted thermal pretreatment process on surface properties, molecular bond characterization of switchgrass, and anaerobic digestion kinetics were also evaluated.

2. Results and Discussion

2.1. Characterization Analysis Results

Characterization of biomass for biofuel production is the first step for evaluation. A field-dried, milled, and homogenized variety of Shawnee as an energy crop was used to characterize biomass. The general composition of switchgrass Shawnee is presented in Table 1, and detailed analysis results can be found in Başar et al. [30]. The variety of Shawnee contained 93.8% dry matter, indicating a moisture content of approximately 6.2%. Volatile solids (VS) were measured as 82.4%, mostly formed of lignocellulose. The lignocellulose composition of switchgrass is quantified as 34.8% hemicellulose, 33.1% cellulose, 26.5% neutral detergent solubles, and 5.6% lignin. Lemusa et al. [33] found 32.6% hemicellulose, 36.8% cellulose, and 6.30% lignin in the switchgrass sample. The results from this study are very close to Lemusa et al.’s [33] findings. Niu et al. [34] and Imam and Capareda [35] have also reported similar results. The elemental composition of the field-dried variety of Shawnee was quantified as 40.13% C, 5.75% H, and 0.87% N, representing switchgrass as a convenient energy crop for biofuel production. Elemental analysis results are in line with the values measured for the switchgrass variety of Shawnee in literature [35,36,37,38]. Furthermore, structural carbohydrate (polymeric carbohydrates, namely cellulose and hemicellulose. Glucose, mannose, galactose, xylose, and arabinose are the monosaccharide component of the cellulose and hemicellulose) analysis resulted that switchgrass variety of Shawnee has 29.41% glucose and 17.36% xylose. The results of the structural carbohydrate analysis were also consistent with the literature [39,40].

2.2. Effect of Ca(OH)2 Assisted Thermal Pretreatment Process on Switchgrass

Thomas et al. [41] indicated that alkaline pretreatments have a variety of effects, such as (i) delignification, which results in the unmasking of cellulose, (ii) the breakdown of hemicellulose and cellulose, and (iii) a reduction in crystalline cellulose. pH, sSugar, and BMP analyses were carried out on raw and pretreated Shawnee switchgrass to observe the pretreatment effect. pH, sSugar, and BMP results of Ca(OH)2-assisted thermal pretreatment experiments are shown in Figure 1a–c, respectively.
Since the Ca(OH)2 is applied in the range of 0–2% in the pretreatment experiments, it is expected that changes in the pretreatment inlet and outlet pHs depend on the applied amount of Ca(OH)2. As can be seen in Figure 1a, the pH values of the variety of Shawnee switchgrass that were not pretreated with Ca(OH)2 at the reaction temperatures of 50, 75, and 100 °C were measured close to each other before and after the pretreatment experiments. While initial pH values were measured as 6.5–6.7, pH values varied between 5.2 and 6.7 depending on solid loading and reaction time after the pretreatment. In the pretreatment experiments assisted with 2% Ca(OH)2, the initial pH values ranged from 10.3 to 10.9. At the end of the reactions, at low temperatures (50 °C), pH values changed in the range of 7.7–8.2 depending on the pretreatment reaction time, while at high temperatures (100 °C), it changed between 6.5 and 6.9 regardless of the reaction time. When 1% Ca(OH)2 was applied in the pretreatments, the initial pH values were 9.5–9.8, while pH values were measured as 6.1–6.8 after the pretreatment. The pH values were observed to be lower at high temperatures.
sSugar analysis found that raw switchgrass has 50 mg sSugar VS−1. The amounts of sSugar were measured at 7% solid loading (SL), as DM is higher than 3% SL when 50 °C reaction temperature, 6 h and 16 h reaction times, and without Ca(OH)2 conditions are applied in the pretreatments. It is normal that sugar’s solubilization from high solid loading was higher than from low solid loading. On the other hand, under the pretreatment conditions of 50 °C reaction temperature, 6 h and 16 h reaction times, and 2% Ca(OH)2, the amount of sSugar at 7% solid loading was lower than 3% solid loading. Higher sSugar values were measured from the raw switchgrass samples at all conditions of 75 °C reaction temperature applied. Furthermore, at 100 °C reaction temperature conditions, the sSugar values measured at 7% SL were higher than those measured at 3% solid loading.
Raw Shawnee switchgrass produced 217.1 mL CH4 gVS−1. In the literature, the methane production potential of switchgrass was reported as 169–252 mL CH4 gVS−1 by Masse et al. [18] and 104.0–153.5 mL gVS−1 by Frigon et al. [16] depending on different harvesting seasons. Furthermore, the methane potential of raw Kanlow was reported as 197.39 mL CH4 gVS−1 by El-Mashad et al. [24], the raw Alamo variety was presented as 246 mL CH4 gVS−1 by Grigatti et al. [42], raw Kanlow was found 215.5 mL CH4 gVS−1 by Başar et al. [30], and raw Shawnee was quantified as 208.4 mL CH4 gVS−1 by Başar and Perendeci [3]. Considering the results in previous studies, obtained results from this study are in the range of reported methane yields.
The maximum methane generation was achieved as 231.4 mL CH4 gVS−1, specifically under the pretreatment conditions of 100 °C reaction temperature, 16 h of reaction time, 0% Ca(OH)2, and 3% solid loading. Methane generation was enhanced by 6.6% compared to raw switchgrass. In contrast, the lowest methane production was observed as 62.4 mL CH4 gVS−1 when the 75 °C reaction temperature, 11 h reaction time, 2% Ca(OH)2, and 5% solid loading pretreatment conditions.
As is seen in Figure 1c, an increase in solid loading from 3% to 7% led to a severe fall in BMP results under all conditions. Zheng et al. [21] observed a similar outcome that mono-digestion of a high dose (>4% TS) of switchgrass led to volatile fatty acid accumulation and process failure, suggesting that a high solid loading might introduce excessive quantities of easily digestible material into digesters.
When 50 °C reaction temperature, 6 h and 16 h reaction times, and 3% solid loading conditions are applied in the pretreatments, an increase in Ca(OH)2 from 0% to 2% resulted in high BMP values. A similar trend was observed at 100 °C reaction temperature, 6 h reaction time, and 3% solid loading conditions, but low BMP production was obtained when raising the reaction time from 6 h to 16 h. Furthermore, BMP values slightly rose or remained stable while the reaction temperature increased from 50 °C to 100 °C. When a reduction in methane production is observed, it should be kept in mind that process optimization is required for the amount of chemicals used in the pretreatment process, depending on the composition of lignocellulose. Gunerhan et al. [43] indicated that the ability to optimize the process within a significant design boundary and assess the positive and negative effects of independent variables and their ranges are compelling qualities in selecting a wide range of independent variables.

2.3. Modeling and Optimization of Ca(OH)2 Assisted Thermal Pretreatment Process

BMP results from the experiments of 51 Ca(OH)2-assisted thermal pretreatment, containing duplicates of 25 varied pretreatment conditions and triplicate of the center point, were loaded into Design Expert software. The model for BMP was developed by RSM. The accuracy of the BMP model was evaluated by the highest determination of coefficient (R2), adjusted-R2, and predicted-R2. In addition, modification (Backward) was applied to the quadratic BMP model to obtain high R2. Backward selection seeks to remove terms from a model that are detrimental to the criterion. p-value criterion was used in the backward selection. The BMP model equation was used to optimize the Ca(OH)2-assisted thermal pretreatment process for maximum methane production with an acceptable process cost. BMP Model equation, statistics, and information are presented in Table 2.
A BMP model with R2 of 0.8572, adjusted–R2 of 0.8121, and predicted–R2 of 0.7646 was developed. The coefficient of determination, expressed as R2, shows the model’s predictive power in percent. The developed model could only explain 85.72% of the relation between BMP and independent variables. The quadratic modified BMP model presented a low probability result (p-value < 0.0001), indicating the model is in the confidence range of 99%. p-values less than 0.05 indicate that model terms are significant. According to the BMP model statistics, solid loading (B) and Ca(OH)2 concentration (D) were found to be significant terms from the first-degree effect terms, whereas reaction time (C) and reaction temperature (A) were determined insignificant terms in the BMP model of Ca(OH)2-assisted thermal pretreatment process. Furthermore, solid loading * Ca(OH)2 concentration (BD), square terms of solid loading (B2), and reaction time (C2) are effective independent variables in the BMP model. Since the first-degree effect of the reaction temperature (A) does not change BMP directly and to obtain a hierarchical model, insignificant terms from the quadratic BMP model were excluded by the application of backward modification.
The individual effects of independent variables of Ca(OH)2 assisted thermal pretreatment process on BMP and desirability (0.977) are presented in Figure 2. The individual effect of each independent variable on the BMP model presents that 179–236 mL CH4 gVS−1 should be produced by the application of 3% solid loading, 6 h reaction time, and 0% Ca(OH)2 concentration conditions in the pretreatment process. As is seen in Figure 2, the BMP value is observed to be stable between the 50 and 100 °C reaction temperature. On the other hand, BMP values decrease from 231.4 to 81.6 mL CH4 gVS−1 by increasing solid loading from 3% to 7%. Furthermore, increasing solid loading, reaction time, and Ca(OH)2 concentration resulted in low desirability and BMP values.
3D response surface plots for the effects of independent variables on the BMP model are given in Figure 3a–d. In the interaction effect of solid loading and reaction temperature presented in Figure 3a, the maximum BMP value was reached only at the lowest solid loading of 3%. The graph also indicates that temperature change did not affect the BMP value where solid loading is kept constant, but the drops in solid loading value remarkably caused a rise in BMP values.
In Figure 3b, the maximum BMP value is also reached only at the lowest solid loading value of 3%. Furthermore, keeping the solid loading at a constant 7% and increasing the Ca(OH)2 concentration positively impacted BMP values. Where solid loading is kept at a constant minimum of 3%, increasing the Ca(OH)2 concentration did not show any significant impact on the methane yield. On the other hand, where Ca(OH)2 concentration was kept at its constant, increasing the solid loading adversely affected the BMP values; specifically, at the maximum solid loading and 0% Ca(OH)2 concentration, BMP resulted in the lowest value. Figure 3c revealed that, within this experimental design, the optimum reaction time is around 6 and/or 16 h to reach the highest methane yield. Between 6 and 16 h reaction time, methane production yield is observed to have a decreasing trend. Figure 3d shows that a change in reaction temperature and Ca(OH)2 concentration in any direction did not affect the BMP values significantly. Conclusively, solid loading * Ca(OH)2 concentration was the most effective interaction for the maximum methane yield.
Optimization of a Ca(OH)2-assisted thermal pretreatment process was implemented to generate the maximum specific methane yield using the BMP model. In the optimization solid loading (%) (+++++), reaction time (h) (+++++), Ca(OH)2 concentration (%) (+++++) were minimized, whereas reaction temperature (°C) (+++++) and BMP yield (mL CH4 g VS−1) (+++++) was maximized. Under these conditions, optimum Ca(OH)2-assisted thermal pretreatment process conditions were found as 3% solid loading, 100 °C reaction temperature, 0% Ca(OH)2 concentration, and 6 h reaction time with the 0.977 value of highest desirability. The BMP model predicted methane yield as 213.5 mL CH4 gVS−1 under optimized conditions. The Ca(OH)2-assisted thermal pretreatment trial was done under optimized conditions for the validation. Pretreated switchgrass was subjected to the BMP test, and methane yield was acquired as 248.7 mL CH4 gVS−1. Enhancement of methane yield was computed as 14.5%, compared to raw switchgrass under optimized validation conditions.
Most of the work in the literature focused on the production of methane from switchgrass without pretreatment. Pretreatment conditions for switchgrass and results available in the literature are presented in Table 3.
It can be concluded from Table 3 that there is limited work focused on the pretreatment of switchgrass for methane production in the literature. Pretreatment work can be classified into two groups. Chemical pretreatment works are supported by the application of heat. Basic (Ca(OH)2, NaOH, KOH), acidic (HCl, H2SO4), and oxidizing (H2O2) chemical agents were preferred in pretreatment. As seen in Table 3, with the pretreatment application, the methane production was 12.2–325.9% enhanced compared to untreated switchgrass [3,4,24,27,31]. Thermal pretreatment as microwave and steam explosion also enriched methane production by 5.2–9.1% [25,26,27,28,29,30,31,32]. Results show that combined chemical and thermal pretreatment application seems to be more effective. The enhancement result obtained in this study is in line with the literature. On the other hand, this work is the first to focus on optimizing Ca(OH)2-assisted thermal pretreatment, considering all the process variables for methane enhancement. However, this result revealed that Ca(OH)2-assisted thermal pretreatment for switchgrass does not significantly affect methane enhancement.

2.4. Effects of Ca(OH)2-Assisted Thermal Pretreatment Process on Switchgrass Surface Modification and Molecular Bond Changes

SEM images and the FTIR analysis of the raw and pretreated switchgrass samples were performed to appraise the alterations in surface properties and the structural-chemical modifications that emerged during the Ca(OH)2-assisted thermal pretreatment process. SEM images of raw switchgrass sample (a), pretreated switchgrass samples at 3% SL, 50 °C, 0% Ca(OH)2, 6 h, (b), 3% SL, 100 °C, 2% Ca(OH)2, 16 h (c), and 3% SL 100 °C, 0% Ca(OH)2, 6 h (d) are presented in Figure 4.
In the SEM image of the raw switchgrass, the sample surface is smooth, compact, and rigid (Figure 4a). Therefore, there is no deformation noticed naturally. On the other hand, the SEM image in Figure 4b reveals that the pretreatment achieves peeling off the outer crust as a function of reaction temperature and time. Additionally, sub-surface canals are observed to begin deterioration. The SEM image of the pretreated switchgrass sample at 3% SL, 2% Ca(OH)2, 16 h, and 100 °C conditions (Figure 4c) indicates how application caused the entire breakdown of the outer crust and sub-surface canals. As a result, the porosity of the material structure has increased, thus enhancing further hydrolysis. Notably, in these conditions, the fibril structure of the switchgrass was entirely altered, and structural unity was distorted. The SEM image of the switchgrass sample at the optimized pretreatment conditions (3% SL, 0% Ca(OH)2, 6 h, and 100 °C) (Figure 4d) shows that the outer crust broke down totally, and slight deterioration is observed on the sub-surface canals.
FTIR spectra of raw switchgrass sample (a), pretreated switchgrass samples at 3% SL, 50 °C, 0% Ca(OH)2, 6 h, (b), 3% SL, 100 °C, 2% Ca(OH)2, 16 h (c), and 3% SL 100 °C, 0% Ca(OH)2, 6 h (d) are presented in Figure 5. Bands in FTIR spectra available in the literature are also given in Table 4 for comparison.
Spectroscopic results obtained by FTIR analysis indicate that raw and pretreated switchgrass samples show similar binding properties at the wavelength between 400 and 1800 cm−1. It is observed that the switchgrass sample pretreated at 3% SL, 100 °C, 2% Ca(OH)2, and 16 h conditions show sectional similarities with the switchgrass sample pretreated at 3% SL, 100 °C, 0% Ca(OH)2, and 6 h conditions. Nevertheless, upon careful examination, differences in chemical bonds were observed in both samples. Between the 400–1800 cm−1 wavelength, 470 cm−1, 560 cm−1, 620 cm−1, 775 cm−1, 895 cm−1, 1050 cm−1, 1180 cm−1, 1245 cm−1, 1440 cm−1, 1465 cm−1, 1580 cm−1 and 1735 cm−1 wavelengths in particular show remarkable differences. FTIR spectrum of raw switchgrass sample shows differences in Si-O-Si and (PO4)3 bonds at 470 cm−1 wavelengths compared to pretreated switchgrass samples. Additionally, a notable resonance in Si-O-Si and (PO4)3 bonds is observed for the switchgrass samples pretreated at 3% SL, 100 °C, 2% Ca(OH)2, and 16 h conditions compared to raw switchgrass, indicating a concentration increase of fragments containing these groups. However, the resonance in C-O and C=O bonds at 620 cm−1 wavelengths remained identical when high temperatures were applied to the switchgrass samples. Thus, this shows how temperature application makes a difference in C-O and C=O bonds. 775 cm−1 wavelength corresponds to resonance in NH2 bonds. Switchgrass samples pretreated at 3% SL, 100 °C, 2% Ca(OH)2, and 16 h conditions have minimum absorbance value compared to raw switchgrass samples. This observation indicates how much deterioration occurred under the effects of Ca(OH)2-assisted temperature pretreatment. Moreover, 895 cm−1 wavelength states the resonance in β-glucosidic bonds directly related to cellulose. Switchgrass sample either pretreated at 3% SL, 50 °C, 0% Ca(OH)2, 6 h, or at 3% SL, 100 °C, 0% Ca(OH)2, 6 h conditions showed similar properties. However, the sample pretreated at 3% SL, 100 °C, 2% Ca(OH)2, and 16 h conditions had a low absorbance value. This is an indication of the deterioration of the β-glycosidic bonds. The 1050 cm−1 wavelength indicates C-O, C=C, C-OH, and C-O-C stretching vibrations in cellulose and hemicellulose compounds. FTIR spectrums of raw and pretreated switchgrass samples at 3% SL, 50 °C, 0% Ca(OH)2, 6 h, and 3% SL, 100 °C, 0% Ca(OH)2, 6 h conditions indicated similar absorbance values. However, a minimum absorbance value was obtained from the switchgrass sample pretreated at 3% SL, 100 °C, 2% Ca(OH)2, and 16 h conditions. This shows the tension in the C-O, C=C, C-OH, and C-O-C bonds of cellulose and hemicellulose. Alteration in the band position and intensity may represent a reduction in the content of the structural ingredients by the application of pretreatment [44]. The peaks at 1180 cm−1 and 1245 cm−1 wavelengths are related to the C-O-C asymmetrical bending vibration in cellulose and hemicellulose compounds and the C-O bonds of acetyl groups of hemicellulose, respectively. Switchgrass samples pretreated at 3% SL, 100 °C, 2% Ca(OH)2, and 16 h conditions resulted in lower absorbance values than others at these wavelengths. This is evidence of the disintegration of the acetyl groups of hemicellulose. In the fingerprint zone of the spectra, modifications in spectra, especially at 1440, 1465, and 1580 cm−1 wavelengths, can be observed from the pretreated switchgrass samples compared to raw switchgrass. Chemical bonds at 1140, 1465, and 1580 are related to lignin decomposition. Out of the fingerprint region, at 2900 and 3400 cm−1 wavelengths, modifications were monitored that indicate an alteration in C-H and O-H bonds.
Table 4. Bands in FTIR spectra available in the literature.
Table 4. Bands in FTIR spectra available in the literature.
Wavelength (cm−1)Affected Chemical Bond and ImpactReference
470Resonance in bonds of Si-O-Si and (PO4)3−[45,46]
620Resonance in C-O, C=O bonds[47]
775Resonance in NH2 bonds[48]
895Resonance in β-glucosidic bonds,
Indicator for crystalline and amorphous cellulose rate
[49,50,51]
1050C-O, C=C, C-OH, and C-O-C tensions in cellulose and hemicellulose[52,53]
1180Asymmetrical C-O-C tension in cellulose and hemicellulose[54]
1245C-O adsorption of acetyl groups in hemicellulose[52]
1280C-H warping in crystallized cellulose[55]
1440O-H bond in linear warping of hemicellulose and lignin[54]
1465C-H deformation in lignin[54]
1580Resonance of aromatic rings in lignin[51]
1735Resonance of bonds in ketone and ester carbonyl groups[55]
2900–3400Resonance and tension of C-H and O-H bonds in cellulose[51,53,56]

2.5. Kinetic Modeling

The BMP test was finalized at 56 days. Since the biogas production reached a plateau after the first 28 days, this period was considered in the kinetic modeling. Predicted methane production and kinetic parameters from the first order, cone, modified Gompertz, and reaction curve modeling, along with the statistical indicators as R2 and Adjusted-R2, are presented in Table 5. Simulated methane potential values were plotted against experimental data to visually compare, shown in Figure 6.
High compatibility (R2) was achieved for all models. All four models were successfully applied to determine the biogas potential of the switchgrass. The hydrolysis rate constant (k) is an important parameter showing the methane production efficiency in the anaerobic degradation process. The k values estimated with the first order kinetic model for the different pretreatments applied to the switchgrass varied in the range of 0.115–0.159 d−1. The k value varies between 0.136 and 0.210 d−1 from cone modeling. Parallel with the first order modeling, the minimum k value was estimated from the pretreated switchgrass at 3% SL, 50 °C, 0% Ca(OH)2, 6 h and was followed by the pretreated switchgrass at 3% SL, 100 °C, 0% Ca(OH)2, 6 h conditions and the raw sample. The estimated and experimental results show a variance between 2.55% and 6.41%. The high R2 values and minor differences between model results and experimental results for methane production indicate that the cone model can be used successfully.
Modified Gompertz modeling results indicate the maximum Rm value would be 17.44 mL CH4 gVS−1 d−1 for pretreated switchgrass at 3% SL, 100 °C, 2% Ca(OH)2, 16 h conditions, 15.97 mL CH4 gVS−1 d−1 for raw sample, 14.37 mL CH4 gVS−1 d−1 from pretreated switchgrass at 3% SL, 100 °C, 0% Ca(OH)2, 6 h, and 14.25 mL CH4 gVS−1 d−1 from pretreated switchgrass at 3% SL, 50 °C, 0% Ca(OH)2, 6 h. Low alpha values are consistent with experimental BMP results. BMP production started quickly in all four samples.
When examining the results of the reaction curve model, the Rm value was calculated as 26.33 mL CH4 gVS−1 d−1 for pretreated switchgrass at 3% SL, 100 °C, 2% Ca(OH)2, 16 h conditions, as in the modified Gompertz model, followed by 22.70 mL CH4 gVS−1 d−1 for raw, 20.33 mL CH4 gVS−1 d−1 from pretreated switchgrass at 3% SL, 100 °C, 0% Ca(OH)2, 6 h, and 20.19 mL CH4 gVS−1 d−1 from pretreated switchgrass at 3% SL, 50 °C, 0% Ca(OH)2, 6 h.
In conclusion, in evaluating the success of each four models in this study, every model achieves applicable results, while first order, cone, and reaction curve methods proved to have a better prediction capacity than modified Gompertz. For the comparison, the effects of pretreatments on methane production kinetic parameters available in the literature are presented in Table 6.
Elalami et al. [7] concluded that the olive pomace maximum methane production rate (Rm) and ultimate specific methane production were improved. At the same time, lag phase time (λ) decreased due to the application of NaOH pretreatment (%2–4–8, 25–50 °C, and 1–2 days), except the lag phase time (λ) for the condition of 8% NaOH, 50 °C and 1 day. Shen et al. [31] applied chemical pretreatments with KOH, NaOH, and Ca(OH)2 to the switchgrass. The λ and maximum methane production rate (μm) values were calculated as 0.8 d and 6.3 mL CH4 gVS−1 d−1, respectively, for 5% Ca(OH)2 pretreatment conditions.
Compared to the untreated raw switchgrass (λ: 3.1 d and μm: 1.9 mLSTP gVS−1 d−1), while λ decreased, the μm value increased by the pretreatment. In this study, parallel with the literature, the Rm value increased, and the λ value decreased obtained from the reaction curve and modified Gompertz models compared to raw by applying 3% SL, 100 °C, 2% Ca(OH)2, 16 h pretreatment condition.
Jackowiak et al. [25] calculated the k value as 0.095–0.134 d−1 for microwave-pretreated switchgrass at different temperatures (90–180 °C). Wu et al. [32] also found k values between 0.021–0.075 d−1 for the leaf and 0.021–0.070 d−1 for the stem part of the switchgrass. Obtained k values from this study are slightly higher than the literature values. However, it should be noted that k values were calculated for the first time for Ca(OH)2-assisted thermal pretreatment for switchgrass.
The cone model uses the kinetic parameters of the hydrolysis rate constant k and the shape factor n to predict methane production Unyay et al. [26] calculated the k and n values as 0.067–0.080 and 1.7–1.9, respectively, for the anaerobic digestion of raw switchgrass at different substrate–inoculum ratios. As a result of the Ca(OH)2-assisted thermal pretreatment in this study, k constants increased, and the n values decreased compared to the work of Unyay et al. [26].

3. Materials and Methods

3.1. Switchgrass

In this study, the switchgrass variety of Shawnee is utilized as biomass. Switchgrass was planted and dried on the field in Karapınar (Konya, Turkey). The size of the samples was reduced to 3 mm to achieve textural homogeneity and consistency [57,58,59,60]. Samples of Shawnee were kept in labware plastic bags at 20 °C temperature for further experimentation for one year.

3.2. Switchgrass Characterization

Total solids (TS), volatile solids (VS) [61], Van Soest detergent fiber [62], structural carbohydrate [63], and elemental analysis were performed to characterize the composition of switchgrass. Measurement of C, H, N, and S content of switchgrass was performed by LECO CHNS-932 Elemental Analyzer (LECO Corporation, St. Joseph, MI, USA). Structural carbohydrate analysis was performed with Thermo Scientific UltiMate® 3000 HPLC (Thermo Fisher Scientific, Waltham, MA, USA) with an Aminex HPX-87P column (Bio-Rad Laboratories Inc., Hercules, CA, USA) for characterization of switchgrass.

3.3. Experimental Design and Analysis

The experimental design of Ca(OH)2-assisted thermal pretreatment on switchgrass was applied by Central Composite Design (CCD) and Response Surface Method (RSM). CCD with 3 levels of 4 independent variables as switchgrass solids loading (3–7%) as DM, reaction temperature (50–100 °C), Ca(OH)2 concentration (0–2%), and reaction time (6–16 h) were designated for the process optimization. Biochemical methane potential (BMP) and sSugar results were selected as dependent variables. Design Expert 11 software (Stat-ease Inc., Minneapolis, MN, USA) was used for experimental design and statistical analysis.
Experimental results were modeled, and the obtained regression model was evaluated by the analysis of variance (ANOVA), regression coefficients, and the p- and F-Values. Model quality was determined by the coefficient of determination (R2) and an adjusted determination coefficient (adj-R2). Optimization of Ca(OH)2-assisted thermal pretreatment was done by using maximization and minimization criteria for independent and dependent variables [64,65] by using obtained model equation. The optimization module investigated the merging of independent variable values that meet the demands placed on each of the dependent variables. The optimizations were performed for maximum methane production potential.

3.4. Ca(OH)2-Assisted Thermal Pretreatment

Ca(OH)2-assisted thermal pretreatment experiments were conducted in 1 L laboratory-scale glass reactors equipped with a reflux condenser immersed in a 2 L oil heating bath. To provide the desired temperature and mixing conditions, magnetic stirrers with heaters (IKA C-Mag HS-7, IKAWerke GmbH, Staufen, Germany) and oil baths were used. Glass reactors were closed with condensers, which were kept at constant temperature by a circulating water bath (Lauda Alpha RA-8, Lauda Dr. R. Wobser GmbH, Lauda-K€onigshofen, Germany) to avoid evaporation.
In the Ca(OH)2-assisted thermal pretreatment experiments, reactors were heated to predetermined temperatures after the addition of a calculated amount of switchgrass, Ca(OH)2, and deionized water. The reaction time was started, and the temperature was kept at the determined temperature during the pretreatment experiments. The reactor contents were continuously mixed with magnetic stirrers at 150 rpm. All pretreatment experiments were performed in duplicates. At the end of reaction time, the temperature of the reactor content was rapidly cooled down to room temperature. pH values of reactor content were measured before and after the pretreatment experiments. Reactor contents were centrifuged two times at 4400 rpm for 5 min and 14,500 rpm for 15 min to obtain the liquid phase for soluble sugar (sSugar) analysis. Soluble sugar (sSugar) analysis was performed by the Dinitro Salicylic Acid (DNS) method [66] to observe the pretreatment efficiency. Mixed solid and liquid samples for BMP tests were kept at −20 °C.

3.5. Biochemical Methane Potential Test (BMP)

The standard BMP test was applied to define the biochemical methane potentials of raw and pretreated switchgrass by Ca(OH)2-assisted thermal. The BMP experiment works on the basis of incubating a specific amount of switchgrass samples mixed with anaerobic sludge at 35 °C and detecting the gas composition and volume produced. The BMP test was conducted according to Perendeci et al. [67]. BMP experiments were performed in 500 mL glass reactors with a 400 mL working volume. pH was set to neutral, and reactors were flushed with N2/CO2 (70%/30%) gas blend for the anaerobic condition after the addition of the switchgrass sample, seed sludge, required nutrients, buffer solution, and deionized water. The substrate-to-seed ratio was selected as 0.5 (gVS gVS−1 for solid samples). BMP reactors were incubated at 35 °C, and experiments were finalized at 56 days. The gas composition of N2, CH4, and CO2 in headspaces of the BMP reactors was quantified by Varian CP-4900 Micro-Gas Chromatography (Varian Inc., Palo Alto, CA, USA). Details of the measurements of biogas volume and the analysis of gas composition can be found in Basar et al. [30].

3.6. Scanning Electron Microscopy (SEM) and Fourier Transform Infrared Spectroscopy (FTIR)

The surface structure of raw and pretreated switchgrass samples was evaluated by SEM to determine the changes caused by Ca(OH)2-assisted thermal pretreatment. Samples firstly were lyophilized and coated with gold-palladium for 120 s under 18 mA current (Polaron SC7620 Sputter Coater, Quorum Technologies, Lewes, UK). After coating, the samples were monitored at different magnifications, and images were kept with SEM (Zeiss Leo 1430, Zeiss Group, Oberkochen, Germany) at 15 kV voltage.
To determine the effects of Ca(OH)2-assisted thermal pretreatment on the molecular bond characteristics of the lignocellulosic structure, Fourier transforms infrared spectroscopy (FTIR) analyzes were performed for both raw and pretreated samples. Samples were lyophilized, and measurements were performed by a Perkin Elmer, Spectrum Two in 400 cm−1 and 4000 cm−1 wavelength ranges.

3.7. Kinetic Modeling

To evaluate the effect of Ca(OH)2-assisted thermal pretreatment on the anaerobic digestion reaction kinetics, specific cumulative methane production was modeled by using modified Gompertz and reaction curve equations. Furthermore, first order and cone models were implemented for the determination of the hydrolysis rate. Detailed descriptions of the model equations can be found in the work of Yılmaz et al. [68]. All model simulations were done by AQUASIM 2.1 Trial version.

4. Conclusions

Energy crops have garnered considerable attention due to their significant potential as biofuel feedstock and agricultural benefits. Most switchgrass varieties are a powerful alternative to produce energy-efficient biofuel. In this study, Ca(OH)2-assisted thermal pretreatment was applied to energy crops to enhance biodegradability and biofuel yield and remove a significant handicap of lignocellulose by unmasking cellulose. Neat optimization revealed that solid loading as DM (3–7%) and Ca(OH)2 concentration (0–2%) were found to be significant independent variables compared to reaction temperature (50–100 °C) and time (6–16 h) within range desing boundary. Essentially, increasing solid loading, reaction time, and Ca(OH)2 concentration resulted in low desirability and methane production yield. A biochemical methane production model was built and validated specific methane yield with 14.5% increases compared to untreated switchgrass. Nevertheless, it is concluded that Ca(OH)2-assisted thermal pretreatment did not significantly affect methane enhancement compared to other pretreatment methods.

Author Contributions

Conceptualization, N.A.P. and H.E.A.; Methodology, H.E.A.; Software, N.A.P. and H.E.A.; Formal Analysis, H.E.A.; Investigation, N.A.P. and H.E.A.; Writing—Original Draft Preparation, N.A.P. and H.E.A., C.E.; Writing—Review and Editing, N.A.P. and H.E.A.; Funding Owner: C.E. and O.Y. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the Project Management Unit of Akdeniz University from Turkey, Grant no: FDK-2017-2501.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Acknowledgments

The authors would like to thank Süleyman Soylu from Konya Selçuk University for help by providing the switchgrass that was used in the study.

Conflicts of Interest

The authors declare no conflict of interest.

Sample Availability

Not available.

References

  1. Debnath, D.; Khanna, M.; Rajagopal, D.; Zilberman, D. The future of biofuels in an electrifying global transportation sector: Imperative, prospects and challenges. Appl. Econ. Perspect. Policy 2019, 41, 563–582. [Google Scholar] [CrossRef]
  2. Brodowska, M.S.; Muszyński, P.; Haliniarz, M.; Brodowski, R.; Kowalczyk-Juśko, A.; Sekutowski, T.; Kurzyna-Szklarek, M. Agronomic aspects of switchgrass cultivation and use for energy purposes. Appl. Ecol. Environ. Res. 2018, 16, 5715–5743. [Google Scholar] [CrossRef]
  3. Başar, İ.A.; Perendeci, N.A. Optimization of zero-waste hydrogen peroxide-Acetic acid pretreatment for sequential ethanol and methane production. Energy 2021, 225, 120324. [Google Scholar] [CrossRef]
  4. Başar, İ.A.; Çoban, Ö.; Göksungur, M.Y.; Eskicioğlu, Ç.; Perendeci, N.A. Enhancement of lignocellulosic biomass anaerobic digestion by optimized mild alkaline hydrogen peroxide pretreatment for biorefinery applications. J. Environ. Manag. 2021, 298, 113539. [Google Scholar] [CrossRef] [PubMed]
  5. Larnaudie, V.; Ferrari, M.D.; Lareo, C. Switchgrass as an alternative biomass for ethanol production in a biorefinery: Perspectives on technology, economics and environmental sustainability. Renew. Sustain. Energy Rev. 2022, 158, 112115. [Google Scholar] [CrossRef]
  6. Alawad, I.; Ibrahim, H. Pretreatment of agricultural lignocellulosic biomass for fermentable sugar: Opportunities, challenges, and future trends. Biomass Convers. Biorefinery 2022, 1–29. [Google Scholar] [CrossRef]
  7. Elalami, D.; Carrere, H.; Abdelouahdi, K.; Garcia-Bernet, D.; Peydecastaing, J.; Vaca-Medina, G.; Oukarroum, A.; Zeroualf, Y.; Barakat, A. Mild microwaves, ultrasonic and alkaline pretreatments for improving methane production: Impact on biochemical and structural properties of olive pomace. Bioresour. Technol. 2020, 299, 122591. [Google Scholar] [CrossRef]
  8. Tian, C.; Yan, M.; Huang, X.; Zhong, Y.; Lu, H.; Zhou, X. Highly acetylated lignocellulose prepared by alkaline extrusion pretreatment assisted acetylation reaction. Cellulose 2022, 29, 1487–1500. [Google Scholar] [CrossRef]
  9. Singh, J.; Suhag, M.; Dhaka, A. Augmented digestion of lignocellulose by steam explosion, acid and alkaline pretreatment methods: A review. Carbohydr. Polym. 2015, 117, 624–631. [Google Scholar] [CrossRef]
  10. Hu, M.; Yua, H.; Lia, Y.; Li, A.; Cai, Q.; Liu, P.; Tu, Y.; Wang, Y.; Hud, R.; Hao, B.; et al. Distinct polymer extraction and cellulose DP reduction for complete cellulose hydrolysis under mild chemical pretreatments in sugarcane. Carbohydr. Polym. 2018, 202, 434–443. [Google Scholar] [CrossRef] [PubMed]
  11. Van Vlierberghe, C.; Escudi, R.; Bernet, N.; Santa-Catalina, G.; Frederic, S.; Carrere, H. Conditions for efficient alkaline storage of cover crops for biomethane production. Bioresour. Technol. 2022, 348, 126722. [Google Scholar] [CrossRef]
  12. Madadi, M.; Wang, Y.; Xu, C.; Liu, P.; Wang, Y.; Xia, T.; Tu, Y.; Lin, X.; Song, B.; Yang, X.; et al. Using Amaranthus green proteins as universal biosurfactant and biosorbent for effective enzymatic degradation of diverse lignocellulose residues and efficient multiple trace metals remediation of farming lands. J. Hazard. Mater. 2021, 406, 124727. [Google Scholar] [CrossRef]
  13. Wu, L.; Feng, S.; Deng, J.; Yu, B.; Wang, Y.; He, B.; Peng, H.; Li, Q.; Hu, R.; Peng, L. Altered carbon assimilation and cellulose accessibility to maximize bioethanol yield under low-cost biomass processing in corn brittle stalk. Green Chem. 2019, 21, 4388. [Google Scholar] [CrossRef]
  14. Thomas, H.; Arnoult, S.; Brancourt-Hulmel, M.; Carrère, H. Methane production variability according to miscanthus genotype and alkaline pretreatments at high solid content. BioEnergy Res. 2019, 12, 325–337. [Google Scholar] [CrossRef]
  15. Kupry´s-Caruk, M.; Podlaski, S.; Kotyrba, D. Influence of double-cut harvest system on biomass yield, quality and biogas production from C4 perennial grasses. Biomass Bioenergy 2019, 130, 105376. [Google Scholar] [CrossRef]
  16. Frigon, J.; Mehta, P.; Guiot, S.R. Impact of mechanical, chemical and enzymatic pre-treatments on the methane yield from the anaerobic digestion of switchgrass. Biomass Bioenergy 2012, 36, 1–11. [Google Scholar] [CrossRef] [Green Version]
  17. Labatut, R.A.; Angenent, L.T.; Scott, N.R. Biochemical methane potential and biodegradability of complex organic substrates. Bioresour. Technol. 2011, 102, 2255–2264. [Google Scholar] [CrossRef]
  18. Masse, D.; Gilbert, Y.; Savoie, P.; Belanger, G.; Parent, G.; Babineau, D. Methane yield from switchgrass and reed canary grass grown in Eastern Canada. Bioresour. Technol. 2011, 102, 10286–10292. [Google Scholar] [CrossRef]
  19. Uma, S.; Thalla, A.K.; Devatha, C.P. Co-digestion of food waste and switchgrass for biogas potential: Effects of process parameters. Waste Biomass Valorization 2020, 11, 827–839. [Google Scholar] [CrossRef]
  20. Zhong, Y.; Chen, R.; Rojas-Sossa, J.P.; Isaguirre, C.; Mashburn, A.; Marsh, T.; Liu, Y.; Liao, W. Anaerobic co-digestion of energy crop and agricultural wastes to prepare uniform-format cellulosic feedstock for biorefining. Renew. Energy 2020, 147, 1358–1370. [Google Scholar] [CrossRef]
  21. Zheng, Z.; Liu, J.; Yuan, X.; Wang, X.; Zhu, W.; Yang, F. Effect of dairy manure to switchgrass co-digestion ratio on methane production and the bacterial community in batch anaerobic digestion. Appl. Energy 2015, 151, 249–257. [Google Scholar] [CrossRef]
  22. Tao, X.; Zhang, P.; Zhang, G.; Nabi, M.; Wang, S.; Ye, J.; Bao, S.; Zhang, Q.; Chen, N. Carbide slag pretreatment enhances volatile fatty acid production in anaerobic fermentation of four grass biomasses. Energy Convers. Manag. 2019, 199, 112009. [Google Scholar] [CrossRef]
  23. Ciggin, A.S. Anaerobic co-digestion of sewage sludge with switchgrass: Experimental and kinetic evaluation. Energy Sources Part A Recovery Util. Environ. Eff. 2016, 38, 15–21. [Google Scholar] [CrossRef]
  24. El-Mashad, H.M. Biomethane and ethanol production potential of Spirulina platensis algae and enzymatically saccharified switchgrass. Biochem. Eng. J. 2015, 93, 119–127. [Google Scholar] [CrossRef]
  25. Jackowiak, D.; Frigon, J.C.; Ribeiro, T.; Pauss, A.; Guiot, S. Enhancing solubilisation and methane production kinetic of switchgrass by microwave pretreatment. Bioresour. Technol. 2011, 102, 3535–3540. [Google Scholar] [CrossRef] [Green Version]
  26. Ünyay, H.; Yılmaz, F.; Başar, İ.A.; Perendeci, N.A.; Çoban, I.; Sahinkaya, E. Effects of organic loading rate on methane production from switchgrass in batch and semi-continuous stirred tank reactor system. Biomass Bioenergy 2022, 156, 106306. [Google Scholar] [CrossRef]
  27. Jin, G.; Bierma, T.; Walker, P.M. Low-heat, mild alkaline pretreatment of switchgrass for anaerobic digestion. J. Environ. Sci. Health-Part A Toxic/Hazard. Subst. Environ. Eng. 2014, 49, 565–574. [Google Scholar] [CrossRef]
  28. Jin, G.; Bierma, T. Low-heat alkaline pretreatment of biomass for dairy anaerobic codigestion. J. Environ. Sci. Health Part B Pestic. Food Contam. Agric. Waste 2014, 49, 786–796. [Google Scholar] [CrossRef]
  29. Jin, G.; Bierma, T.; Walker, P.M. Biogas production from switchgrass under experimental conditions simulating U.S. digester operations. J. Environ. Sci. Health-Part A Toxic/Hazard. Subst. Environ. Eng. 2012, 47, 470–478. [Google Scholar] [CrossRef]
  30. Başar, İ.A.; Kokdemir Ünsar, E.; Ünyay, H.; Perendeci, N.A. Ethanol, methane, or both? Enzyme dose impact on ethanol and methane production from untreated energy crop switchgrass varieties. Renew. Energy 2020, 149, 287–297. [Google Scholar] [CrossRef]
  31. Shen, J.; Zhang, J.; Wang, W.; Liu, G.; Chen, C. Assessment of pretreatment effects on anaerobic digestion of switchgrass: Economics-energy-environment (3E) analysis. Ind. Crops Prod. 2020, 145, 111957. [Google Scholar] [CrossRef]
  32. Wu, C.; Zhou, H.; Yang, F.; Zhang, Y.; Gao, F. Microwave pretreatments of switchgrass leaf and stem fractions to increase methane production. Bioresources 2015, 10, 3922–3933. [Google Scholar] [CrossRef] [Green Version]
  33. Lemusa, E.R.; Brummer, C.; Moore, K.J.; Molstad, N.E.; Burras, C.E.; Barker, M.F. Biomass yield and quality of 20 switchgrass populations in southern Iowa, USA. Biomass Bioenergy 2002, 23, 433–442. [Google Scholar] [CrossRef]
  34. Niu, H.; Kong, X.; Li, L.; Sun, Y.; Yuan, Z.; Zhou, X. Analysis of Biogas from Switchgrass by Anaerobic Digestion. Bioresources 2015, 10, 7178–7187. [Google Scholar] [CrossRef] [Green Version]
  35. Imam, T.; Capareda, S. Characterization of Bio-Oil, Syn-Gas and Bio-Char From Switchgrass Pyrolysis at Various Temperatures. J. Anal. Appl. Pyrolysis 2011, 93, 170–177. [Google Scholar] [CrossRef]
  36. Masnadi, M.S.; Habibi, R.; Kopyscinski, J.; Hill, J.M.; Bi, X.; Lim, C.J.; Ellis, N.; Grace, J.R. Fuel characterization and co-pyrolysis kinetics of biomass and fossil fuels. Fuel 2014, 117, 1204–1214. [Google Scholar] [CrossRef]
  37. Sadaka, S.; Sharara, M.A.; Ashworth, A.; Keyser, P.; Allen, F.; Wright, A. Characterization of Biochar from Switchgrass Carbonization. Energies 2014, 7, 548–567. [Google Scholar] [CrossRef]
  38. Vassilev, S.V.; Vassileva, C.G.; Baxer, D. Trace element concentrations and associations in some biomass ashes. Fuel 2014, 129, 292–313. [Google Scholar] [CrossRef]
  39. Papa, G.; Rodriguez, S.; George, A.; Schievano, A.; Orzi, V.; Sale, K.L.; Singh, S.; Adani, F.; Simmons, B.A. Comparison of different pretreatments for the production of bioethanol and biomethane from corn stover and switchgrass. Bioresour. Technol. 2015, 183, 101–110. [Google Scholar] [CrossRef]
  40. Athmanathan, A.; Emery, I.R.; Kuczek, T.; Mosier, N.S. Impact of temperature, moisture, and storage duration on the chemical composition of switchgrass, corn stover, and sweet sorghum bagasse. Bioenergy Res. 2015, 8, 843–856. [Google Scholar] [CrossRef]
  41. Thomas, H.L.; Nolasco, H.F.P.; Carrère, H.; Lartaud, M.; Cao, T.V.; Baptiste, C.; Verdei, J.L. Alkaline Pretreatments for Sorghum and Miscanthus Anaerobic Digestion: Impacts at Cell Wall and Tissue Scales. BioEnergy Res. 2022, 15, 792–809. [Google Scholar] [CrossRef]
  42. Grigatti, M.; Barbanti, L.; Pritoni, G.; Venturi, G. Comparison of switchgrass (Panicum virgatum L.) genotypes as potential energy crop. In Proceedings of the 2nd World Conference and Technology Exhibition on Biomass for Energy, Industry and Climate Protection, Rome, Italy, 10–14 May 2004; Available online: https://www.researchgate.net/publication/235781180_COMPARISON_OF_SWITCHGRASS_Panicum_virgatum_L_GENOTYPES_AS_POTENTIAL_ENERGY_CROP (accessed on 25 February 2022).
  43. Günerhan, Ü.; Us, E.; Dumlu, L.; Yılmaz, V.; Carrère, H.; Perendeci, A.N. Impacts of Chemical-Assisted Thermal Pretreatments on Methane Production from Fruit and Vegetable Harvesting Wastes: Process Optimization. Molecules 2020, 25, 500. [Google Scholar] [CrossRef] [Green Version]
  44. Dar, R.A.; Phutela, U.G. Enzymatic and hydrothermal pretreatment of newly isolated Spirulina subsalsa BGLR6 biomass for enhanced biogas production. Waste Biomass Valorization 2020, 11, 3639–3651. [Google Scholar] [CrossRef]
  45. Saikia, B.J.; Parthasarathy, G. Fourier Transform Infrared Spectroscopic Characterization of Kaolinite from Assam and Meghalaya, Northeastern India. J. Mod. Phys. 2010, 1, 206–210. [Google Scholar] [CrossRef] [Green Version]
  46. Uysal, I.; Severcan, F.; Evis, Z. Characterization by Fourier transform infrared spectroscopy of hydroxyapatite co-doped with zinc and fluoride. Ceram. Int. 2013, 39, 7727–7733. [Google Scholar] [CrossRef]
  47. Litescu, S.C.; Teodor, E.D.; Truica, G.I.; Tach, A.; Radu, G.L. Fourier Transform Infrared Spectroscopy–Useful Analytical Tool for Non-Destructive Analysis. Infrared Spectrosc.-Mater. Sci. Eng. Technol. 2012, 353–368. [Google Scholar]
  48. Sumayya, A.; Panicker, C.Y.; Varghese, H.T.; Harikumar, B. Vibrational spectroscopic studies and AB inition calculations of l-glutamic acid 5-amide. RJC Rasayan J. Chem. 2008, 1, 548–555. [Google Scholar]
  49. Chandrasekaran, S.R.; Hopke, P.K.; Rector, L.; Allen, G.; Lin, L. Chemical composition of wood chips and wood pellets. Energy Fuels 2012, 26, 4932–4937. [Google Scholar] [CrossRef]
  50. Sun, C.; Liu, R.; Cao, W.; Yin, R.; Mei, Y.; Zhang, L. Impacts of Alkaline Hydrogen Peroxide Pretreatment on Chemical Composition and Biochemical Methane Potential of Agricultural Crop Stalks. Energy Fuels 2015, 29, 4966–4975. [Google Scholar] [CrossRef]
  51. Fu, S.F.; Wang, F.; Yuan, X.Z.; Yang, Z.M.; Luo, S.J.; Wang, C.S.; Guo, R.B. The thermophilic (55 °C) microaerobic pretreatment of corn straw for anaerobic digestion. Bioresour. Technol. 2015, 175, 203–208. [Google Scholar] [CrossRef]
  52. Ang, T.N.; Ngoh, G.C.; Seak, A.; Chua, M.; Lee, M.G. Elucidation of the effect of ionic liquid pretreatment on rice husk via structural analyses Elucidation of the effect of ionic liquid pretreatment on rice husk via structural analyses. Biotechnol. Biofuels 2012, 5, 1–10. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  53. Xu, F.; Yu, J.; Tesso, T.; Dowell, F.; Wang, D. Qualitative and quantitative analysis of lignocellulosic biomass using infrared techniques: A mini-review. Appl. Energy 2013, 104, 801–809. [Google Scholar] [CrossRef]
  54. Xu, F.; Sun, J.; Sun, R.; Fowler, P.; Baird, M.S. Comparative study of organosolv lignins from wheat straw. Ind. Crops Prod. 2006, 23, 180–193. [Google Scholar] [CrossRef]
  55. Gokulakumar, B.; Narayanaswamy, R. Fourier Transform–Infrared Spectra (FT-IR) Analysis of Root Rot Disease in Sesame (Sesamum Indicum). Rom. J. Biophys. 2008, 18, 217–223. [Google Scholar]
  56. Hsu, T.C.; Guo, G.L.; Chen, W.H.; Hwang, W.S. Effect of dilute acid pretreatment of rice straw on structural properties and enzymatic hydrolysis. Bioresour. Technol. 2010, 101, 4907–4913. [Google Scholar] [CrossRef] [PubMed]
  57. Del Campo, I.; Alegria, I.; Zazpe, M.; Echeverria, M.; Echeverria, I. Diluted acid hydrolysis pretreatment of agri-food wastes for bioethanol production. Ind. Crops Prod. 2006, 24, 214–221. [Google Scholar] [CrossRef]
  58. Buffiere, P.; Loisel, D.; Bernet, N.; Delgenes, J.P. Towards new indicator for the prediction of solid waste anaerobic digestion properties. Water Sci. Technol. 2006, 53, 233–241. [Google Scholar] [CrossRef] [Green Version]
  59. Xu, Z.; Wang, Q.; Jiang, Z.; Yang, X.; Ji, Y. Enzymatic hydrolysis of pretreated soybean straw. Biomass Bioenergy 2007, 31, 162–167. [Google Scholar] [CrossRef]
  60. Cara, C.; Ruiz, E.; Oliva, J.M.; Saez, F.; Castro, E. Conversion of olive tree biomass into fermentable sugars by dilute acid pretreatment and enzymatic saccharification. Bioresour. Technol. 2008, 99, 1869–1876. [Google Scholar] [CrossRef] [PubMed]
  61. AWWA; WEF; APHA. Standard methods: 2540. In Standard Methods for the Examination of Water and Wastewater, 23rd ed.; Water Environment Federation: Alexandria, VA, USA, 1997; pp. 55–61. [Google Scholar]
  62. Van Soest, P.J. Use of detergent in the analysis of fibrous feeds. A rapid method for the determination of fibre and lignin. J. Assoc. Anal. Chem. 1963, 46, 829e35. [Google Scholar]
  63. Sluiter, A.; Hames, B.; Ruiz, R.; Scarlata, C.; Sluiter, J.T.; Crocker, D. Determination of structural carbohydrates and lignin in biomass determination of structural carbohydrates and lignin in biomass. Lab. Anal. Proced. 2012, 17. [Google Scholar]
  64. Perendeci, N.A.; Gokgol, S.; Orhon, D. Impact of alkaline H2O2 pretreatment on methane generation potential of greenhouse crop waste under anaerobic conditions. Molecules 2018, 23, 1794. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  65. Perendeci, N.A.; Ciggin, A.S.; Kokdemir Ünşar, E.; Orhon, D. Optimization of alkaline hydrothermal pretreatment of biological sludge for enhanced methane generation under anaerobic conditions. Waste Manag. 2020, 107, 9–19. [Google Scholar] [CrossRef]
  66. Miller, G.L. Use of dinitrosalicylic reagent for determination of reducing sugar. Anal. Chem. 1959, 31, 426–428. [Google Scholar] [CrossRef]
  67. Perendeci, N.A.; Yilmaz, V.; Taştan, B.E.; Gökgö, S.; Fardinpoor, M.; Namlı, A.; Steyer, J.P. Correlations between biochemical composition and biogas production during anaerobic digestion of microalgae and cyanobacteria isolated from different sources of Turkey. Bioresour. Technol. 2019, 281, 209–216. [Google Scholar] [CrossRef]
  68. Yilmaz, F.; Kökdemir Ünşar, E.; Perendeci, N.A.; Sahinkaya, E. Energy generation from multifarious wastes of alcohol distillery raki production process: Kinetic modeling of methane production. J. Environ. Chem. Eng. 2021, 9, 104838. [Google Scholar] [CrossRef]
Figure 1. Ca(OH)2-assisted thermal pretreatment effects on pH (a), sSugar (b) and BMP (c).
Figure 1. Ca(OH)2-assisted thermal pretreatment effects on pH (a), sSugar (b) and BMP (c).
Molecules 27 06891 g001aMolecules 27 06891 g001b
Figure 2. Desirability and BMP prediction values related to independent process variables as reaction temperature (a), solid loading (b), reaction time (c), and Ca(OH)2 concentration (d).
Figure 2. Desirability and BMP prediction values related to independent process variables as reaction temperature (a), solid loading (b), reaction time (c), and Ca(OH)2 concentration (d).
Molecules 27 06891 g002
Figure 3. 3D response surface plots for the effects of independent variables on BMP. The response surface diagrams: (a) Solid loading-Reaction time, (b) Solid loading-Ca(OH)2 concentration, (c) Reaction time-Reaction temperature, (d) Ca(OH)2 concentration-Reaction Temperature.
Figure 3. 3D response surface plots for the effects of independent variables on BMP. The response surface diagrams: (a) Solid loading-Reaction time, (b) Solid loading-Ca(OH)2 concentration, (c) Reaction time-Reaction temperature, (d) Ca(OH)2 concentration-Reaction Temperature.
Molecules 27 06891 g003
Figure 4. SEM images of raw switchgrass sample (a), Pretreated switchgrass sample 3% SL, 50 °C, 0% Ca(OH)2, 6 h, (b) Pretreated switchgrass sample 3% SL, 100 °C, 2% Ca(OH)2, 16 h (c), and Pretreated switchgrass sample 3% SL, 100 °C, 0% Ca(OH)2, 6 h (d).
Figure 4. SEM images of raw switchgrass sample (a), Pretreated switchgrass sample 3% SL, 50 °C, 0% Ca(OH)2, 6 h, (b) Pretreated switchgrass sample 3% SL, 100 °C, 2% Ca(OH)2, 16 h (c), and Pretreated switchgrass sample 3% SL, 100 °C, 0% Ca(OH)2, 6 h (d).
Molecules 27 06891 g004
Figure 5. FTIR spectra of raw switchgrass sample, Pretreated switchgrass sample 3% SL, 50 °C, 0% Ca(OH)2, 6 h, Pretreated switchgrass sample 3% SL, 100 °C, 2% Ca(OH)2, 16 h, and Pretreated switchgrass sample 3% SL, 100 °C, 0% Ca(OH)2, 6 h.
Figure 5. FTIR spectra of raw switchgrass sample, Pretreated switchgrass sample 3% SL, 50 °C, 0% Ca(OH)2, 6 h, Pretreated switchgrass sample 3% SL, 100 °C, 2% Ca(OH)2, 16 h, and Pretreated switchgrass sample 3% SL, 100 °C, 0% Ca(OH)2, 6 h.
Molecules 27 06891 g005
Figure 6. Model predictions and experimental methane productions (a) pretreated switchgrass at 3% SL, 100 °C, 2% Ca(OH)2, 16 h; (b) pretreated switchgrass at 3% SL, 50 °C, 0% Ca(OH)2, 6 h; (c) pretreated switchgrass at 3% SL, 100 °C, 0% Ca(OH)2, 6 h and (d) raw switchgrass.
Figure 6. Model predictions and experimental methane productions (a) pretreated switchgrass at 3% SL, 100 °C, 2% Ca(OH)2, 16 h; (b) pretreated switchgrass at 3% SL, 50 °C, 0% Ca(OH)2, 6 h; (c) pretreated switchgrass at 3% SL, 100 °C, 0% Ca(OH)2, 6 h and (d) raw switchgrass.
Molecules 27 06891 g006
Table 1. Characterization analysis results of Shawnee.
Table 1. Characterization analysis results of Shawnee.
ComponentResultStd. Dev.
Solid
Total Solid, TS (g kg−1 Sample)938.120.54
Volatile Solid, VS (g kg−1 Sample)824.313.36
Van Soest Fractions
Neutral Detergent Solubles (%)26.540.48
Hemicellulose (%)34.760.36
Cellulose (%)33.130.44
Acid Detergent Lignin (%)5.570.39
Elemental Analysis
Carbon, C (%)40.13
Hydrogen, H (%)5.75
Nitrogen, N (%)0.87
Sulfur, S (%)-
Total Structural Carbohydrates (%)52.860.559
Cellobiose (%)0
Glucose (%)29.410.347
Xylose (%)17.360.167
Galactose (%)3.230.018
Arabinose (%)2.870.027
Mannose (%)0
Table 2. Model equation and statistics for biochemical methane potential (BMP).
Table 2. Model equation and statistics for biochemical methane potential (BMP).
Biochemical Methane Potential Model (Modified, Reduced Quadratic)
SourceSum of SquaresDegree of FreedomMean SquareF-Valuep-Value
Model83,292.64613,882.1119.01<0.0001
B-Solid loading (SL, wt.%) as DM43,543.01143,543.0159.63<0.0001
C-Reaction time (h)65.62165.620.08990.7676
D-Ca(OH)2 conc. (wt.%)3625.8013625.804.970.0381
BD4480.4714480.476.140.0228
B25584.9015584.907.650.0123
C25819.1115819.117.970.0109
Residual13,874.9119730.26
Lack of Fit13,260.1818736.681.200.6269
Pure Error614.731614.73
Cor Total97,167.5425
Fit Statistics
Standard Deviation (Std. Dev.)27.02R20.8572
Mean134.21Adjusted R20.8121
Coefficient of Variation (CV)20.13Predicted R20.7646
Adequate Precision10.7861
Model Equation in Terms of Coded Factors
(mL CH4gVS−1) = +76.47 − 49.18 × B − 1.91 × C + 14.19 × D + 16.73 × BD + 41.28 × B² + 42.13 × C²
Table 3. Pretreatment conditions for switchgrass and results available in the literature.
Table 3. Pretreatment conditions for switchgrass and results available in the literature.
Applied PretreatmentPretreatment ConditionsResultsReference
Ca(OH)2 Assisted ThermalChemicals: Ca(OH)2: 0–2%
Solid Loading: 3–7%
Reaction Temperature: 50–100 °C
Reaction Time: 6–16 h
BMP Raw Switchgrass (Shawnee): 217.1 mL CH4 gVS−1
CH4 Yield at Optimized Conditions: 248.7 mL CH4 gVS−1 at 3% solid loading as DM, 0% Ca(OH)2, 100 °C, 6 h.
Enhancement Compared to Raw Switchgrass: 14.5%
This Work
H2O2 and Acetic Acid (Hac) Assisted ThermalChemicals: H2O2: 0–2% and Hac: 0–2%
Reaction Temperature: 50–100 °C
Reaction Time: 6–24 h
BMP Raw Switchgrass (Shawnee): 195.5 mL CH4 gVS−1
CH4 Yield at Optimized Conditions: 342.63 mL CH4 gVS−1 at 1.87% Hac, 0% H2O2, 50 °C, 6 h.
Enhancement Compared to Raw Switchgrass: 75.2%
[3]
H2O2 Assisted ThermalChemicals: H2O2 1–3%
Solid loading: 3–7%
Reaction Temperature: 50–100 °C
Reaction Time: 6–24 h
BMP Raw Switchgrass: 208.4 mL CH4 gVS−1
CH4 Yield at Optimized Conditions: 291.34 mL CH4 gVS−1 at 6.43% solid loading, 1.83% H2O2, 50 °C, 6.78 h.
Enhancement Compared to Raw Switchgrass: 39.8%
[4]
Chemical Pretreatment
(NaOH, KOH, Ca(OH)2, H2O2, HCl, H2SO4)

Steam Explosion
Chemical Pretreatment
Chemicals: NaOH, KOH, Ca(OH)2, H2O2, HCl, H2SO4
2, 3, 4, 5% w/v.
Reaction Temperature: 25 °C
Reaction Time: 12 h
Solid loading: 8% (200 g Switchgrass/2.5 L)
Steam Explosion
Pressure: 1.2, 1.5, 1.8 Mpa
Time: 20 Min.
BMP Raw Switchgrass: 46.3 mL CH4 gVS−1
CH4 Yield at Optimized Conditions: 197.2 mL CH4 gVS−1 at 4% NaOH, 25 °C, 12 h.
Enhancement Compared to Raw Switchgrass: 325.9%
CH4 Yield from Pretreated with 5% Ca(OH)2: 90.0 mL CH4 gVS−1
The effect of Ca(OH)2 pretreatment was not desirable compared to NaOH and KOH pretreatments.
[31]
Microwave Pretreatment Final Reaction Temperature: 100, 150, 180 °C
Reaction Time: 0–10–20 min.
Temperature Increase: 5, 7.5, 10 °C/min
BMP Raw Switchgrass (Alamo): -mL CH4 gVS−1
CH4 Yield of Switchgrass Leaf at Optimized Conditions: 134.81 mL CH4 gVS−1 at 100 °C, 10 min, and 7.5 °C/min.
Enhancement Compared to Raw Leaf Switchgrass: 9.1%
CH4 Yield of Switchgrass Stem at Optimized Conditions: 99.35 mL CH4 gVS−1 at 150 °C, 10 min, and 10 °C/min.
Enhancement Compared to Raw Stem Switchgrass: 5.2%
[32]
Chemical and Enzymatic Pretreatment Chemical Pretreatment
Chemicals: NaOH 1% (w/v)
Liquid: Solid Ratio:10:1
Reaction Temperature: 50 °C
Reaction Time: 12 h
Enzymatic Pretreatment
Reaction Time: 72 h
Reaction Temperature: 50 °C
Enzymes: Novozyme®188 (Cellobiase from Aspergillus niger) 35 FPU
Celluclast®1.5 L (Cellulase from Tricho-derma reesei ATCC 26921) 61.5 CBU
BMP Raw Switchgrass (Kanlow): 197.39 mL CH4 gVS−1
CH4 Yield of Chemically Pretreated Switchgrass: 255.35 mL CH4 gVS−1
Enhancement Compared to Raw Switchgrass: 29.4%
CH4 Yield of Chemically and Enzymatically Pretreated Switchgrass: 373.03 mL CH4 gVS−1
Enhancement Compared to Raw Switchgrass: 89%
[24]
Low Heat and Chemical PretreatmentChemicals: NaOH, Ca(OH)2, H2O2
0, 2.2, 5.5, 11, 22% NaOH, 6.6%H2O2
Reaction Temperature: Room Temp—100 °C
Reaction Time: 3, 6, 24 h
BMP of Fine Grind Raw Switchgrass (Cave-in-Rock): 296 mL CH4 gVS−1 CH4 Yield of Switchgrass at Optimized Condition: 332 mL CH4 gVS−1 at 5.5% NaOH, 100 °C, 6 h.
Enhancement Compared to Raw Switchgrass: 12.2%
[27]
Microwave Pretreatment Reaction Temperature: 90–180 °C
Reaction Time: 7.5–32.6 Min.
BMP of Fine Grind Raw Switchgrass (Kanlow): 296 mL CH4 gVS−1
CH4 Yield of Switchgrass at Optimized Condition: 320 mL CH4 gVS−1 at 150 °C
Enhancement Compared to Raw Switchgrass: 8.1%
Microwave pretreatment induced no significant effect on methane production.
[25]
Table 5. Predicted methane production and kinetic parameters from the models.
Table 5. Predicted methane production and kinetic parameters from the models.
ModelParameterSwitchgrass
Pretreated atPretreated atPretreated atRaw
3% SL, 100 °C, 2% Ca(OH)2, 16 h3% SL, 50 °C, 0% Ca(OH)2, 6 h3% SL 100 °C, 0% Ca(OH)2, 6 h
M (mL CH4 gVS−1added)176.9164.05178.26199.31
First Orderk (d−1)0.1590.1150.1220.145
Ppredicted (mL CH4 gVS−1added)173.92161.68170.88188.71
R20.9880.9940.9920.985
Adjusted R20.9860.9930.9910.984
Difference (%)1.681.454.145.31
Conek (d−1)0.210.1360.1650.183
n1.1091.3281.3031.341
Ppredicted (mL CH4 gVS−1added)169.5159.87166.82188.9
R20.9930.9970.9920.983
Adjusted R20.9920.9960.9910.982
Difference (%)4.182.556.415.22
Modified GompertzRm (mL CH4 gVS−1added d−1)17.4414.2514.3715.97
λ (day)0.0110.0640.030.023
Ppredicted (mL CH4 gVS−1added)171.34154.17169.89192.51
R20.9540.9840.9670.976
Adjusted R20.9490.9820.9630.973
Difference (%)3.146.024.693.41
Reaction CurveRm (mL CH4 gVS−1added d−1)26.3320.1920.3322.7
λ (day)0.0180.0590.040.038
Ppredicted (mL CH4 gVS−1added))178.3160.67174.4199.71
R20.990.9940.9920.986
Adjusted R20.9890.9940.9920.984
Difference (%)−0.792.062.16−0.2
Table 6. Effects of pretreatments on methane production kinetic parameters available in the literature.
Table 6. Effects of pretreatments on methane production kinetic parameters available in the literature.
SampleKinetic ParametersResultsReference
Switchgrass
s-CSTR
First Order (FO)
Cone (C)
Modified Gompertz (MG)
Reaction Curve (RC)
FO: k: −0.046–0.054 d−1
C: n: 1.7–1.9
MG: Rm: 7.1–9.3 mL CH4 gVS−1 d−1
RC: Rm: 9.45–12.6 mL CH4 gVS−1 d−1
[26]
The Olive Pomace
Alkaline Pretreatment (NaOH: 2%, 4% and 8% (w/w TS))
Microwave
NaOH + Microwave
Modified GompertzUntreated Raw:
Rm: 21.8 mL CH4 gVS−1 d−1
λ: 3.8 d
NaOH Pretreatment:
Rm: 22.4–50.9 mL CH4 gVS−1 d−1
λ: 0–5.6 d
[7]
Switchgrass
Chemical Pretreatment
(NaOH, Ca(OH)2)
Modified GompertzSampleμm (mL CH4 gVS−1 d−1)λ (d)[31]
Untreated SG1.93.1
4% NaOH17.92
5% Ca(OH)26.30.8
Switchgrass
Microwave Pretreatment
(90–180 °C)
First Orderk: 0.080–0.134
The increase in the pretreatment temperature caused an increase in the k coefficient, except for 105 °C. The SG biodegradability accelerated. The 105 °C pretreatments showed similar results to the raw sample.
[25]
Microwave Pretreatment
Leaf and Stem fraction
First OrderLeaf–k: 0.021–0.075 d−1
Stem–k: 0.021–0.070 d−1
The k values were increased by 44% and 68% at 150 °C and 180 °C, respectively, compared with the control.
[32]
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Akman, H.E.; Perendeci, N.A.; Ertekin, C.; Yaldiz, O. Energy Crops and Methane: Process Optimization of Ca(OH)2 Assisted Thermal Pretreatment and Modeling of Methane Production. Molecules 2022, 27, 6891. https://doi.org/10.3390/molecules27206891

AMA Style

Akman HE, Perendeci NA, Ertekin C, Yaldiz O. Energy Crops and Methane: Process Optimization of Ca(OH)2 Assisted Thermal Pretreatment and Modeling of Methane Production. Molecules. 2022; 27(20):6891. https://doi.org/10.3390/molecules27206891

Chicago/Turabian Style

Akman, Hasmet Emre, Nuriye Altınay Perendeci, Can Ertekin, and Osman Yaldiz. 2022. "Energy Crops and Methane: Process Optimization of Ca(OH)2 Assisted Thermal Pretreatment and Modeling of Methane Production" Molecules 27, no. 20: 6891. https://doi.org/10.3390/molecules27206891

APA Style

Akman, H. E., Perendeci, N. A., Ertekin, C., & Yaldiz, O. (2022). Energy Crops and Methane: Process Optimization of Ca(OH)2 Assisted Thermal Pretreatment and Modeling of Methane Production. Molecules, 27(20), 6891. https://doi.org/10.3390/molecules27206891

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