Next Article in Journal
One-Dimensional Compressibility and Creep Characteristics of Unsaturated Compacted Loess Based on Incremental Loading and Constant Rate of Strain Methods
Previous Article in Journal
Water-Richness Zoning Technology of Karst Aquifers at in the Roofs of Deep Phosphate Mines Based on Random Forest Model
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

The Influence of Pyrolysis Time and Temperature on the Composition and Properties of Bio-Oil Prepared from Tanjong Leaves (Mimusops elengi)

1
Postgraduate School of Engineering Studies, Universitas Syiah Kuala, Banda Aceh 23111, Indonesia
2
Department of Chemical Engineering, Faculty of Engineering, Universitas Malikussaleh, Lhokseumawe 24355, Indonesia
3
Department of Chemical Engineering, Faculty of Engineering, Universitas Syiah Kuala, Banda Aceh 23111, Indonesia
4
Reaction Engineering and Catalysis Laboratory, Department of Chemical Engineering, Faculty of Engineering, Universitas Syiah Kuala, Banda Aceh 23111, Indonesia
5
Department of Physics Education, Faculty of Teacher Training and Education, Universitas Syiah Kuala, Banda Aceh 23111, Indonesia
*
Author to whom correspondence should be addressed.
Sustainability 2023, 15(18), 13851; https://doi.org/10.3390/su151813851
Submission received: 18 August 2023 / Revised: 9 September 2023 / Accepted: 12 September 2023 / Published: 18 September 2023

Abstract

:
This research aims to evaluate the influence of pyrolysis time and temperature on the composition and properties of bio-oil derived from Mimusops elengi. Experiments were conducted by varying the pyrolysis temperature and time from 400 to 600 °C and 30 to 120 min, respectively. Both pyrolysis temperature and time were found to significantly influence the bio-oil composition. At enhanced pyrolysis temperatures, the bio-oil yield increased while the ash and gas yields decreased. In addition, extended pyrolysis time produced a greater bio-oil yield, indicating that higher temperatures and longer durations promote additional decomposition of biomass. Functional groupings, including alcohols, phenols, ketones, esters, and aromatic compounds in the bio-oil, were identified via FT-IR analysis, indicating that the bio-oil’s diversified chemical properties make it a potential alternative feedstock. GC-MS analysis identified 26 chemical compounds in the bio-oil, of which phenol was the most abundant. However, a high phenol content can diminish bio-oil quality by enhancing acidity, decreasing heating value, and encouraging engine corrosion. Temperature and pyrolysis time are crucial factors in producing bio-oil with the desired chemical composition and physical properties. The maximum yield, 34.13%, was attained after 90 min of operation at 500 °C. The characteristics of the Mimusops elengi bio-oil produced, namely density, viscosity, pH, and HHV were 1.15 g/cm3, 1.60 cSt, 4.41, and 19.91 MJ/kg, respectively, in accordance with ASTM D7544. Using Mimusops elengi as a pyrolysis feedstock demonstrates its potential as an environmentally friendly energy source for a variety of industrial and environmental applications. The yield of bio-oil produced is not optimal due to the formation of tar, which results in the blockage of the output flow during the pyrolysis process.

1. Introduction

In a period of globalization, along with rapid growth in population and developing technology, energy demands and the number of energy sources are increasing daily. Actual statistics and severe forecasts on the future demand for fossil resources (even though their usage has led to environmental concerns) testify to the need for more sustainable energy, industrial, and agricultural policies, prompting researchers to seek cleaner energy sources [1,2,3]. The primary objective of the renewable energy program is to increase environmentally favorable energy production by applying innovative technology [4,5,6]. As the demand for renewable energy increases, biomass has emerged as a crucial renewable energy source with a good reputation due to its availability and carbon neutrality. Among the numerous varieties of biomass, agricultural waste (crop residue) is gaining increasing prominence as a potential source of bioenergy in an agro-economy, as it consists predominantly of leaves and stems, constitutes a lignocellulosic biomass, and is a suitable feedstock for biorefineries to generate value-added biomaterials and bioenergy (sustainability fuels) [7].
Several valuable plants grow naturally in Southeast Asian nations; most dwell in suburbs, cities, and agricultural areas [8]. Mimusops elengi is one of the sources of agricultural residue biomass in Banda Aceh (Aceh, Indonesia). These plants are native trees from India, Myanmar, and Sri Lanka that have been in the archipelago for centuries [9,10,11]. Banda Aceh (Indonesia) currently has around 6500 Mimusops elengi plants across an area of 28.2 ha [12]. According to the literature, these types of plants have been used widely for various purposes, with encouraging outcomes. All parts of the Mimusops elengi plant have been studied for medical purposes, including the roots, skin, foliage, flowers, and leaves, and it may even be used as biodiesel (bioenergy) [13,14,15,16]. The Mimusops elengi biomass residues, particularly the leaves, can be utilized as an alternative energy source if handled appropriately. This residual biomass (leaves) could be used for energy or converted into liquid via a pyrolysis process due to it containing carbon (38.50%), hydrogen (5.23%), cellulose (33.17%), and lignin (10.24%) [17]. It is also noted in the literature that biomass with high cellulose content has the potential to be used as raw material in bioenergy production [18,19,20,21]. To the best of our knowledge, there is a limited number of reports on utilizing and converting Mimusops elengi leaves (waste) via thermal pyrolysis into value-added compounds (bio-oils). However, it is crucial to emphasize that the potential of agricultural residues (waste) for bioenergy must be observed locally, depending on the environmental factors in a particular location.
Pyrolysis is a thermochemical process (300–700 °C) that makes it possible to convert biomass to bio-oil, biochar, and non-condensable gases [22,23]. Generally, bio-oil is a dark brown liquid fuel with a smoke-like stench that comes from condensing lignin-rich pyrolysis vapor, cellulose, and other carbon compounds [24]. Bio-oil contains alcohol, phenols, organic acids, and carbonyls as its principal organic compounds. It has a slightly lower fuel value than diesel and other light fuel oils but a slightly higher fuel value than other oxygen-based fuels (such as methanol). Even though the pyrolysis of biomasses has been investigated with numerous categories of biomass, such as wood [25,26], agricultural waste [19,27,28,29,30,31], and domestic and industrial waste [32], until now, no prior research has been conducted on the pyrolysis of Mimusops elengi for producing bio-oil. Therefore, in this research, the Mimusops elengi biomass (leaves) is investigated as a raw material for producing bio-oil as a renewable energy source.
In most previous investigations, different parameters (reaction times and temperatures) were altered to identify the optimal range of bio-oil results. The most suitable temperature for each experiment was 400–600 °C, with reaction durations ranging from 20 min to 3 h [23,33,34]. Even now, few studies have defined the phenomena and issues most commonly associated with the product distribution behavior (functional groups and chemical composition) of bio-oil products at various temperatures and reaction times in the pyrolysis process, particularly regarding Mimusops elengi residues (leaves). The objectives of this study were to gain a deeper comprehension of the product distribution behavior in bio-oils derived from Mimusops elengi leaves (waste) during the thermal-pyrolysis process (temperature = 300–500 °C; time = 30–120 min) through gas chromatography–mass spectroscopy (GC-MS) and Fourier-transform infrared spectroscopy (FT-IR) analyses. For the purpose of obtaining an understanding of the Mimusops elengi biomass’s (leaves’) characteristics, the material’s properties, such as volatile matter, moisture, fixed carbon, and ash, as well as the amounts of carbon (C), hydrogen (H), nitrogen (N), and oxygen (O), are examined via proximate and ultimate analyses. Along with this issue being discussed, the bio-oil’s properties, such as pH, density, viscosity, and calorific value (HHV), were extensively examined.

2. Materials and Methods

2.1. Material and Sample Preparation

The biomass used was Mimusops elengi, which was obtained from around Darussalam and Banda Aceh (5.565547 N and 95.367807 E). Mimusops elengi was first cleaned under running water and dried in the sun for about three days. The dried Mimusops elengi was cut into small pieces. It was then put in the oven at 105 °C for 24 h with the aim of removing the water content from the Mimusops elengi. The Mimusops elengi that had been dried in the oven was ground and sieved to a mesh size of 40. The proximate analysis consisted of the determination of ash, moisture, and fixed carbon content in accordance with ASTM standards (D1102-84, D2016-74, D3178-89, and D3175-07 for ash, moisture, fixed carbon, and volatile matter [35,36,37,38], respectively). Employing an elemental analyzer using Unicube Organic Matter Analyzer, United States, the C, N, H, and S of Mimusops elengi biomass samples were calculated. Using Equation (1), the oxygen content of the biomass samples was determined, and the results are presented in Table 1.
O (%) = 100 − (ash + sulfur + nitrogen + hydrogen + carbon)
The heating value was obtained using the elemental analysis results. High calorific value (HHV) and low calorific value (LHV) are the two primary calorific value categories. The difference between HHV and LHV is equal to the water vaporization heat produced by fuel combustion. Mott and Spooner’s modification of the Dulong-type formula was used to derive the high heating value of bio-oil [39,40,41]. Generally, the HHV and LHV formulations are employed when the oxygen concentration exceeds 15%, which is shown in Equations (2) and (3).
HHV (MJ/kg) = 0.3417 C + 0.1232 S + 1.3221 H − 0.1198 (O + N) − 0.0153 A
LHV (MJ/kg) = HHV − (0.218 × H)
where C, H, O, N, S, and A are the mass percents of carbon, hydrogen, oxygen, nitrogen, sulfur, and ash in the material, respectively.

2.2. Pyrolysis Process

The pyrolysis apparatus consists of a fluidized bed reactor, a condenser, and a furnace with a temperature controller. The reactor is made of stainless steel and has a biomass raw material capacity of 40 g. The biomass-filled reactor is placed in the furnace, the furnace is sealed, and inert gas is injected into the reactor for approximately 10 min before being turned off [42]. Nitrogen is utilized as an inert gas. Nitrogen’s function is to eliminate confined air in the reactor, leaving the reactor devoid of air.
Experiments were conducted with varying temperatures of 300, 350, 400, 450, and 500 °C and pyrolysis durations of 30, 60, 90, and 120 min. The yields of bio-oil, biochar, and gas can be calculated using the formulas % bio-oil yield (% dry weight), % biochar yield (% dry weight), and % gas yield (% dry weight) [43,44,45]. The pyrolysis employed in this experiment is depicted in Figure 1.

2.3. Bio-Oil Characteristics

Biomass from Mimusops elengi is pyrolyzed to produce bio-oil, a liquid with a reddish-black hue. As shown in Table 2, the bio-oil’s characteristics were analyzed in accordance with ASTM 7544-12 to ascertain its physical properties [38]. According to ASTM D240, the heating value measurement was conducted using a bomb calorimeter [46]. The GC-MS Shimadzu QP 2010 Plus (Kyoto, Japan) was used to determine the chemical composition of Mimusops elengi bio-oil, and the FT-IR Shimadzu IRPrestige-21 (Kyoto, Japan) was used to identify the bio-oil’s functional groups. Meanwhile, the decomposition of Mimusops elengi caused by heat was investigated using thermogravimetric analysis and differential thermogravimetric analysis (TGA-DTG Perkin Elmer STA 6000) (Waltham, MA, USA).

3. Results

3.1. Characterization of Mimusops elengi

3.1.1. Proximate and Ultimate Analyses

The proximate and ultimate analyses of Mimusops elengi provide a deeper understanding of the characteristics of this biomass and how these characteristics affect the pyrolysis process and the quality of the bio-oil produced. The proximate analysis revealed that the Mimusops elengi biomass had a moisture content of 12%, a volatile matter content of 62.35%, a fixed carbon content of 21.16%, and an ash content of 5.49%. High water content can affect the quality of the bio-oil produced because high water content in bio-oil can cause a low heating value [47,48]. However, excess moisture content can also help reduce the viscosity of bio-oil and reduce NOx emissions [49].
Furthermore, volatile components of the Mimusops elengi biomass have a major effect on the bio-oil yield produced via pyrolysis. The greater the proportion of volatile components in biomass, the greater the bio-oil yield. This volatile component can be broken down by heat into vapor, which is then condensed into bio-oil [43,50,51]. In addition, the fixed carbon and ash content of the Mimusops elengi biomass additionally affect bio-oil production. High fixed carbon can increase char production, whereas high ash content can decrease bio-oil yield [51]. Therefore, the Mimusops elengi biomass, which has low fixed carbon and ash content, is suitable for bio-oil production via the pyrolysis process.
The ultimate analysis of the Mimusops elengi biomass revealed carbon, nitrogen, hydrogen, sulfur, and oxygen content of 45.91%, 1.64%, 6.42%, 0.26%, and 40.28%, respectively. The high carbon and hydrogen content indicates the potential for high calorific value in the bio-oil produced [52]. During the pyrolysis process, oxygen binds to hydrocarbon molecules and forms oxygenated compounds that can degrade the quality of the bio-oil. Therefore, a Mimusops elengi biomass with low oxygen content produces bio-oil with better quality. In addition, the low nitrogen and sulfur content in the Mimusops elengi biomass indicates that the bio-oil produced has a low potential for the formation of NOx and SOx, which are harmful to the environment.
By comparing the results of the proximate and ultimate analyses of the Mimusops elengi biomass, it can be deduced that this biomass has excellent prospects for bio-oil production via pyrolysis. The biomass of Mimusops elengi has a moderate water content, a high volatile material content, and a low fixed carbon and ash content, suggesting that it can produce bio-oil yields of a high quality and quantity. Moreover, the hydrogen content and high carbon content of the Mimusops elengi biomass imply that it could be harnessed to produce bio-oil with a high calorific value. By reducing the oxygen, nitrogen, and sulfur content of the biomass, it is possible to ensure that the bio-oil produced is of higher quality and less damaging to the environment.

3.1.2. Thermogravimetric Analysis

Figure 2 depicts the mass change and mass change rate of Mimusops elengi as a function of temperature with TGA and DTG graphs. At the beginning of the test, the mass of the Mimusops elengi leaves decreased gradually over a low temperature range (28–222 °C) and a short time (0–270 s). This decrease is due to the evaporation of the moisture content and light volatile matter present in the biomass. Then, in the intermediate temperature range (192–497 °C) with a longer time (271–658 s), lignocellulose decomposition occurred in the Mimusops elengi. It was seen that there was a significant increase in the rate of mass change at a given temperature, which indicated a more intense decomposition reaction. Furthermore, at temperatures within 250 and 350 °C, hemicellulose decomposition occurred, followed by cellulose decomposition at 350 to 450 °C. At this temperature range, levoglucosan was formed as the main pyrolysis product. It was seen that the rate of mass change reached its peak at a specific temperature, indicating a peak in decomposition activity. At higher temperatures (300–900 °C) [29,30], lignin decomposition occurred in the Mimusops elengi. The graph shows that the rate of mass change decreases significantly at these high temperatures, signaling slower decomposition of lignin.
From Figure 2, it can be seen that the decomposition of Mimusops elengi reaches its peak at a temperature of about 470 °C and a time of 359.11 s, where the most significant mass change occurs. This temperature can be regarded as the optimum temperature for the decomposition of the Mimusops elengi biomass in the pyrolysis process. The TGA and DTG analyses provide a deeper understanding of the Mimusops elengi biomass’s decomposition patterns. This information can be used to optimize pyrolysis parameters, such as temperature and time, to achieve efficient biomass decomposition and produce bio-oil of the desired quality.

3.1.3. Influence of Pyrolysis Temperature

The influence of pyrolysis temperature on the biomass of Mimusops elengi was investigated, and the results are depicted in Figure 3. The graph depicts the variations in the percentages of bio-oil, char, and gas products at various pyrolysis temperatures (300, 350, 400, 450, and 500 °C). At 300 °C, the lowest pyrolysis temperature, the decomposition process is slow and char is the primary by-product. The bio-oil yield at 300 °C was 18.32%, while the char yield was high at 46%. However, as the temperature rose from 300 °C to 500 °C, the yield of condensable bio-oil increased until a maximum of 34.14% was attained. Higher pyrolysis temperatures enhance the heating rate and lignin degradation, thereby increasing bio-oil production. In addition, with the increase in the temperature, the biochar produced decreased from 46% down to 25%. However, the yield of bio-oil decreases when the temperature exceeds the optimal range. This decrease is due to the decomposition of volatile substances into gases and tar into gases and char. The bio-oil yield increased from 18.32% at 300 °C to 34.13% at 500 °C. This can be attributed to the decomposition of lignin at 250–500 °C, which is the main contribution of bio-oil in the pyrolysis process [23,33].
In contrast, as the temperature rises, the yield of char decreases. Rises in temperature lead to a reduction in char yield due to the increased degradation of Mimusops elengi and char residues. Conversely, gas yield increases as the temperature increases. The spike in gas production is expected to be caused primarily by the secondary breakdown of pyrolysis vapor at elevated temperatures.
In addition to the percentages of bio-oil, char, and gas products, it is also necessary to pay attention to the quality of the products produced, which is affected by the pyrolysis temperature. At lower pyrolysis temperatures, bio-oil tends to have a higher moisture content and a lower viscosity. Conversely, at higher temperatures, bio-oil has a lower moisture content and a higher viscosity. In addition, pyrolysis temperature can also affect the chemical composition of the bio-oil produced. At lower temperatures, bio-oils tend to have higher levels of fatty acids and aldehydes. However, at higher temperatures, aromatic components such as phenol and catechol tend to increase.

3.1.4. Influence of Pyrolysis Time

In addition to the influence of temperature, the pyrolysis time also has a significant impact on the pyrolysis yield of Mimusops elengi. At a pyrolysis process time of 30 min, the yields of bio-oil, char, and gas products were 23.23%, 28.83%, and 47.94%, respectively. It can be seen that at this relatively short pyrolysis time, the biomass decomposition process is not entirely complete. However, when the pyrolysis process time was extended to 90 min, the yields of bio-oil, char, and gas increased to 34.13%, 21.04%, and 44.83%, respectively. This also happened in the previous study, which used palm shell biomass. At 20 min, the yields of bio-oil, char, and gas products were 61%, 30%, and 7% wt., respectively, while at 30 min, the yields of bio-oil, char, and gas products increased. This increase in yield can be explained by the length of the secondary reaction time, which allows the decomposition of lignin into hydrocarbons to be maximized [53].
The increase in bio-oil yield along with the increase in pyrolysis time show that a longer pyrolysis time provides an opportunity for the chemical reaction to last longer, resulting in better conversion of biomass into bio-oil. The longer pyrolysis process also allows for more efficient decomposition of lignin into hydrocarbon compounds. In addition, it should be noted that the effect of time on gas yield does not show significant changes. Although there are slight fluctuations in gas yield, the difference is not very noticeable between 30 and 120 min. This suggests that reaction time appears to have little effect on gas yield in a given time frame. In the context of longer pyrolysis times, it is also necessary to pay attention to the possibility of excessive thermal degradation, which may reduce the quality of bio-oil products and lead to the formation of unwanted by-products. Therefore, optimization of the pyrolysis time becomes an important factor in achieving maximum bio-oil yield with the desired quality.

3.2. Characterization of Bio-Oil from Mimusops elengi

The bio-oil produced by the pyrolysis of Tanjung leaves has a distinctive reddish-black hue and an acrid odor, as shown in Figure 4. It possesses the characteristics enumerated in Table 3. Viscosity is a measurement of a fluid’s resistance to flow, and is affected by variables such as temperature, pressure, and impurities. The viscosity of a substance increases with increasing temperature and reaction time, which indicates that the substance becomes more resistant to flow as it is subjected to reactions at a higher temperature and for a longer time. This can be attributed to the fact that increasing temperature and reaction time can cause the molecules of a substance to become closer together and have more difficulty moving past one another, resulting in a higher viscosity [44]. Viscosity is an important property of fluids that can affect their behavior in various applications, such as lubrication, mixing, and pumping. For example, fluids with high viscosity may require more energy to pump or mix, while fluids with low viscosity may not provide sufficient lubrication or protection in certain applications. Therefore, understanding the viscosity of a substance under different conditions can be important for optimizing its use in various applications. Mimusops elengi bio-oil has a viscosity between 1.31 and 1.60 cSt at 40 °C. As a consequence of the bio-oil’s high water content, its viscosity is reduced. The water content of the bio-oil is affected by the lignin content of the Tanjung biomass. The rise and fall in viscosity may be due to component degradation. During pyrolysis, the components of bio-oil may undergo thermal degradation. This is also caused by the uneven water content in the biomass. Bio-oil’s energy content depends on its density. The density of bio-oil at 15 °C ranges between 1.1 and 1.3 kg/m3. At 15 °C, the density of Mimusops elengi bio-oil ranges from 1.12 to 1.15 kg/m3. Bio-oil’s density depends on its composition [45]. The pH value of Mimusops elengi bio-oil at room temperature ranges from 4.0 to 4.4. The pH of the bio-oil obtained is similar to the pH of the bio-oil from previous studies [53,54]. Bio-oil’s low pH is a result of the acidity of its composition. Bio-oil is acidic because of its breakdown of hemicellulose and cellulose from the biomass, resulting in a high oxygen content. In terms of direct use or application, the high acidity of bio-oil is detrimental to the product, as it can cause the crushing of constituents during crushing and application [55]. This must be considered in the storage process and production system for the materials used [27].
Calorific value is a crucial consideration in determining a bio-oil’s application. The chemical composition of the material itself also influences the HHV value. A composition with a higher concentration of high-energy or combustible organic compounds will have a greater HHV. The HHV of Mimusops elengi-derived bio-oil ranges between 6.76 and 19.91 MJ/kg. The HHV of biomass samples complies with the findings of the proximate and ultimate tests based on these results. In addition, previous research has demonstrated that biomass with high levels of cellulose and lignin has an averagely higher HHV value [56]. According to [47,56], lignin has a higher HHV than either cellulose or starch. During pyrolysis, the calorific value of biomass does not always alter the calorific value of bio-oil. This is due to the fact that different forms of biomass with the same calorific value contain different quantities of lignocellulose, volatile matter, and fixed carbon. As a result, under different pyrolysis and biomass conditions, the lignocellulose turns into condensed vapor (bio-oil) [57,58,59].

3.3. Chemical Composition Based on FT-IR Analysis

Figure 5 and Table 4 show the FT-IR spectra of the bio-oil obtained from the pyrolysis of Mimusops elengi at 500 °C and 90 min, which are the best pyrolysis parameters, with wavelengths between 4000 and 500 cm−1. Based on the results of the FT-IR analysis, several functional groups can be identified in the Mimusops elengi bio-oil. In the frequency range between 3584–3700 cm−1 and 3300–3400 cm−1, there is O-H stretching of the hydroxyl groups of alcohol, phenol, methanol, and ethanol, which are carboxyl groups that bind to aromatic rings in bio-oil. In addition, the occurrence of C-H stretching in the frequency ranges 2850–3000 cm−1 and 2815–2880 cm−1 indicates the presence of alkanes. The absorption band between 2815 and 2850 cm−1 is most likely due to the overlapping C-H bands of ethanol and methanol. The peaks detected between 2100 and 2140 cm−1 are indicative of C≡C stretching vibrations that form alkyne compounds, whereas the peaks between 1700 and 1790 cm−1 can be attributed to the strong C=O stretching of aldehydes and ketones. The peak between 1620 and 1680 cm−1 indicates the presence of variable C=C and moderate vibrational stretching in alkenes and aromatic compounds. Strong stretching vibrations between 1250 and 1310 cm−1 indicate the presence of ether (O=C–O–C). The peak at 1035–1085 cm−1 indicates the presence of primary and tertiary alcohols due to the elongation of the strong C-O bond. The alkenes’ C–H vibrations could elicit an absorbance peak between 610 and 700 cm−1. These functional groups are also present in bio-oils from other types of biomasses [60,61,62,63].
Based on the FT-IR spectra of the bio-oil, it can be seen that the Mimusops elengi bio-oil contains various functional groups that are typical in chemical compounds. The content of alcohols, phenols, alkanes, methyl, ketones, aldehydes, carboxylic acids, aromatic derivatives, and other compounds can be detected through this FT-IR analysis. By knowing the composition of the functional groups, information about the types of chemical compounds contained in the bio-oil can be obtained. These data are vital in evaluating the quality of bio-oil produced from the pyrolysis process of Mimusops elengi.

3.4. Chemical Composition Based on GC-MS Analysis

The bio-oil derived from the pyrolysis of Mimusops elengi is a complex mélange of phenols, ketones, alcohol, nitrogen-containing compounds, ethers, aromatic hydrocarbon acids, furans, and esters. Table 5 shows the composition of edible oil from the pyrolysis of Mimusops elengi, with the following chromatography conditions: oven temp: 31 °C, injection temp: 270 °C, injection mode: split, flow control mode: linear, and total flow: 71.2 mL/min. A total of 26 chemical compounds were identified in the bio-oil from Mimusops elengi. In Figure 6, the predominant compound identified in the bio-oil from the pyrolysis of Mimusops elengi is phenol, which is derived from the decomposition of lignin [64]. In all bio-oils from energy crops, phenol is the most abundant compound in bio-oils obtained from lignin decomposition [65]. Phenol compounds contain 42% methoxy, 35% benzenediol, and 21% alkyl phenols. The lignin content in Mimusops elengi is 10.24%. However, the lignin content in Mimusops elengi is lower than in rice husk at 33.7% [66,67]. Bio-oil derived from Mimusops elengi contains 64.2% phenol. As a fuel, the elevated phenol content has several negative effects. High levels of phenolic compounds can increase the acid number, decrease the heating value, lower the pH level, and increase the engine corrosion value.
The study of the chemical composition of bio-oil derived from the pyrolysis of Mimusops elengi is facilitated by the discovery of these compounds. Various properties and qualities of bio-oils, such as acid value, thermal stability, calorific value, and combustion properties, can be altered by these compounds. For the evaluation and development of the prospective use of bio-oil as an alternative energy source, a comprehensive understanding of the compounds contained in bio-oil is essential.

4. Conclusions

In this study, the pyrolysis of Mimusops elengi was carried out at a temperature of 300–500 °C and a time of 30–120 min, and the resulting bio-oil was characterized. The optimum conditions for the pyrolysis of Mimusops elengi were 500 °C for 90 min at 34.13%, which were relatively similar to bio-oil yield conditions from other agricultural residues. The bio-oil’s physical properties as a vegetable oil, such as density, viscosity, pH, and HHV—1.15 g/cm3, 1.60 cSt, 4.41, and 19.91 MJ/kg, respectively—conform to the bio-oil standard. The resulting bio-oil had a wide range of functional groups, including phenols, acids, carbonyls, and hydrocarbons, which were detected via FT-IR and GC-MS analysis. FT-IR and GC-MS additionally showed that phenolic compounds are the predominant component of bio-oil derived from the pyrolysis of Mimusops elengi, indicating that the Mimusops elengi biomass is suited to being used as a source of renewable energy. Further research to explore the potential of Mimusops elengi in the fields of energy and the environment can be performed by adding catalysts.

Author Contributions

Conceptualization, methodology, investigation, formal analysis, writing—original draft, L.M.; conceptualization, supervision, writing—review and editing, validation, H.H.; conceptualization, writing—review and editing, N.A. and C.M.R.; writing—review and editing, M.S. and N.; writing—review and editing, formal analysis, F.N. and A. All authors have read and agreed to the published version of the manuscript.

Funding

This work is supported by the Indonesian Ministry of Education, Culture, Research, and Technology Indonesia (Kemdikbudristekdikti) under the grant obtained through the Doctoral Dissertation Research (PDD) contract number 4/UN11.2.1/PT.01.03/DPRM/2022.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Acknowledgments

The authors are grateful to the Indonesian Ministry of Education, Culture, Research, and Technology Indonesia for financial support, and to the Chemical Engineering Department, Faculty of Engineering at Universitas Syiah Kuala for technical support.

Conflicts of Interest

The authors declare that they have no known competing financial interests or personal relationships that could be perceived as having influenced the work stated in this paper.

References

  1. Yong, J.Y.; Klemeš, J.J.; Varbanov, P.S.; Huisingh, D. Cleaner Energy for Cleaner Production: Modelling, Simulation, Optimisation and Waste Management. J. Clean. Prod. 2016, 111, 1–16. [Google Scholar] [CrossRef]
  2. Nasution, F.; Husin, H.; Mahidin; Abnisa, F.; Tirta Yani, F.; Maulinda, L.; Ahmadi. Conversion of Pyrolysis Vapors Derived from Non-Biodegradable Waste Plastics (PET) into Valuable Fuels Using Nickel-Impregnated HZSM5-70 Catalysts. Energy Convers. Manag. 2022, 273, 116440. [Google Scholar] [CrossRef]
  3. Guizani, C.; Valin, S.; Billaud, J.; Peyrot, M.; Salvador, S. Biomass Fast Pyrolysis in a Drop Tube Reactor for Bio Oil Production: Experiments and Modeling. Fuel 2017, 207, 71–84. [Google Scholar] [CrossRef]
  4. Nižetić, S.; Djilali, N.; Papadopoulos, A.; Rodrigues, J.J.P.C. Smart Technologies for Promotion of Energy Efficiency, Utilization of Sustainable Resources and Waste Management. J. Clean. Prod. 2019, 231, 565–591. [Google Scholar] [CrossRef]
  5. Rizal, T.A.; Khairil, T.A.; Mahidin, T.A.; Husin, H.; Ahmadi, H.; Nasution, F.; Umar, H. The Experimental Study of Pangium Edule Biodiesel in a High-Speed Diesel Generator for Biopower Electricity. Energies 2022, 15, 5405. [Google Scholar] [CrossRef]
  6. Husin, H.; Erdiwansyah, E.; Ahmadi, A.; Nasution, F.; Rinaldi, W.; Abnisa, F.; Mamat, R. Efficient Hydrogen Production by Microwave-Assisted Catalysis for Glycerol-Water Solutions via NiO/Zeolite-CaO Catalyst. S. Afr. J. Chem. Eng. 2022, 41, 43–50. [Google Scholar] [CrossRef]
  7. Balogun, A.O.; Lasode, O.A.; McDonald, A.G. Thermochemical and Pyrolytic Analyses of Musa Spp. Residues from the Rainforest Belt of Nigeria. Environ. Prog. Sustain. Energy 2018, 37, 1932–1941. [Google Scholar] [CrossRef]
  8. Mudryk, K.; Jewiarz, M.; Wróbel, M.; Niemiec, M.; Dyjakon, A. Evaluation of Urban Tree Leaf Biomass-Potential, Physico-Mechanical and Chemical Parameters of Raw Material and Solid Biofuel. Energies 2021, 14, 818. [Google Scholar] [CrossRef]
  9. Sayed, D.F.; Afifi, A.H.; Temraz, A.; Ahmed, A.H. Metabolic Profiling of Mimusops Elengi Linn. Leaves Extract and in Silico Anti-Inflammatory Assessment Targeting NLRP3 Inflammasome. Arab. J. Chem. 2023, 16, 104753. [Google Scholar] [CrossRef]
  10. Shahwar, D.; Raza, M.A. Antioxidant Potential of Phenolic Extracts of Mimusops Elengi. Asian Pac. J. Trop. Biomed. 2012, 2, 547–550. [Google Scholar] [CrossRef]
  11. Kar, B.; Kumar, R.B.S.; Karmakar, I.; Dola, N.; Bala, A.; Mazumder, U.K.; Hadar, P.K. Antioxidant and in Vitro Anti-Inflammatory Activities of Mimusops Elengi Leaves. Asian Pac. J. Trop. Biomed. 2012, 2, S976–S980. [Google Scholar] [CrossRef]
  12. Haris, M.; Dedy; Suryatmojo, H.D. Polda Aceh Tanam 6.500 Pohon Penghijauan Di Aceh Besar. Available online: https://aceh.antaranews.com/berita/116183/polda-aceh-tanam-6500-pohon-penghijauan-di-aceh-besar (accessed on 9 September 2023).
  13. Srinivasan, G.R.; Palani, S.; Munir, M.; Saeed, M.; Jambulingam, R. Biodiesel Production from Mimusops Elengi Seed Oil through Means of Co-Solvent-Based Transesterification Using an Ionic Liquid Catalyst. In Biofuel from Microbes and Plants; CRC Press: Boca Raton, FL, USA, 2021. [Google Scholar]
  14. GR, S.; Palani, S.; Ranjitha, J. Biodiesel Production from the Seeds of Mimusops Elengi Using Potassium Aluminium Silicate as Novel Catalyst. Innov. Energy Res. 2017, 6, 165. [Google Scholar] [CrossRef]
  15. Meriatna; Husin, H.; Riza, M.; Faisal, M.; Ahmadi; Sulastri. Biodiesel Production Using Waste Banana Peel as Renewable Base Catalyst. Mater. Today Proc. 2023, 87, 214–217. [Google Scholar] [CrossRef]
  16. Husin, H.; Abubakar, A.; Ramadhani, S.; Sijabat, C.F.B.; Hasfita, F. Coconut Husk Ash as Heterogenous Catalyst for Biodiesel Production from Cerbera Manghas Seed Oil. In MATEC Web of Conferences; EDP Sciences: Castanet-Tolosan, France, 2018. [Google Scholar]
  17. Kalita, D.; Saikia, C.N. Chemical Constituents and Energy Content of Some Latex Bearing Plants. Bioresour. Technol. 2004, 92, 219–227. [Google Scholar] [CrossRef] [PubMed]
  18. Biswas, B.; Pandey, N.; Bisht, Y.; Singh, R.; Kumar, J.; Bhaskar, T. Pyrolysis of Agricultural Biomass Residues: Comparative Study of Corn Cob, Wheat Straw, Rice Straw and Rice Husk. Bioresour. Technol. 2017, 237, 57–63. [Google Scholar] [CrossRef] [PubMed]
  19. Qiu, B.; Tao, X.; Wang, J.; Liu, Y.; Li, S.; Chu, H. Research Progress in the Preparation of High-Quality Liquid Fuels and Chemicals by Catalytic Pyrolysis of Biomass: A Review. Energy Convers. Manag. 2022, 261, 115647. [Google Scholar] [CrossRef]
  20. Yin, M.; Bi, D.; Zhao, W.; Liu, J.; Zhao, A.; Jiang, M. Production of Bio-Oil and Biochar by the Nitrogen-Rich Pyrolysis of Cellulose with Urea: Pathway of Nitrile in Bio-Oil and Evolution of Nitrogen in Biochar. J. Anal. Appl. Pyrolysis 2023, 174, 106137. [Google Scholar] [CrossRef]
  21. Zhong, D.; Zeng, K.; Li, J.; Qiu, Y.; Flamant, G.; Nzihou, A.; Vladimirovich, V.S.; Yang, H.; Chen, H. Characteristics and Evolution of Heavy Components in Bio-Oil from the Pyrolysis of Cellulose, Hemicellulose and Lignin. Renew. Sustain. Energy Rev. 2022, 157, 111989. [Google Scholar] [CrossRef]
  22. Wang, F.; Zheng, Y.; Huang, Y.; Yang, X.; Liu, C.; Kang, J.; Zheng, Z. Effect of Temperature on Characteristics of Bio-Oil and Bio-Char during Pyrolysis of Yunnan Pine. J. Biobased Mater. Bioenergy 2016, 10, 81–89. [Google Scholar] [CrossRef]
  23. Jamilatun, S.; Elisthatiana, Y.; Aini, S.N.; Mufandi, I.; Budiman, A. Effect of Temperature on Yield Product and Characteristics of Bio-Oil From Pyrolysis of Spirulina Platensis Residue. Elkawnie 2020, 6, 96–108. [Google Scholar] [CrossRef]
  24. Dai, L.; Zeng, Z.; Tian, X.; Jiang, L.; Yu, Z.; Wu, Q.; Wang, Y.; Liu, Y.; Ruan, R. Microwave-Assisted Catalytic Pyrolysis of Torrefied Corn Cob for Phenol-Rich Bio-Oil Production over Fe Modified Bio-Char Catalyst. J. Anal. Appl. Pyrolysis 2019, 143, 104691. [Google Scholar] [CrossRef]
  25. Fahmy, T.Y.A.; Fahmy, Y.; Mobarak, F.; El-Sakhawy, M.; Abou-Zeid, R.E. Biomass Pyrolysis: Past, Present, and Future. Environ. Dev. Sustain. 2020, 22, 17–32. [Google Scholar] [CrossRef]
  26. Zhang, L.; Bao, Z.; Xia, S.; Lu, Q.; Walters, K.B. Catalytic Pyrolysis of Biomass and Polymer Wastes. Catalysts 2018, 8, 659. [Google Scholar] [CrossRef]
  27. Abnisa, F.; Wan Daud, W.M.A.; Sahu, J.N. Optimization and Characterization Studies on Bio-Oil Production from Palm Shell by Pyrolysis Using Response Surface Methodology. Biomass Bioenergy 2011, 35, 3604–3616. [Google Scholar] [CrossRef]
  28. Azzaharo, F.; Mardiyati, Y.; Steven; Rizkiansyah, R.R. Ekstraksi Serat Kulit Jagung Sebagai Bahan Baku Benang Tekstil. Maj. Polim. Indones. 2015, 18, 21–25. [Google Scholar]
  29. Balagurumurthy, B.; Srivastava, V.; Vinit; Kumar, J.; Biswas, B.; Singh, R.; Gupta, P.; Kumar, K.L.N.S.; Singh, R.; Bhaskar, T. Value Addition to Rice Straw through Pyrolysis in Hydrogen and Nitrogen Environments. Bioresour. Technol. 2015, 188, 273–279. [Google Scholar] [CrossRef] [PubMed]
  30. Cai, W.; Liu, R.; He, Y.; Chai, M.; Cai, J. Bio-Oil Production from Fast Pyrolysis of Rice Husk in a Commercial-Scale Plant with a Downdraft Circulating Fluidized Bed Reactor. Fuel Process. Technol. 2018, 171, 308–317. [Google Scholar] [CrossRef]
  31. Duman, G.; Okutucu, C.; Ucar, S.; Stahl, R.; Yanik, J. The Slow and Fast Pyrolysis of Cherry Seed. Bioresour. Technol. 2011, 102, 1869–1878. [Google Scholar] [CrossRef]
  32. Mohan, D.; Pittman, C.U.; Steele, P.H. Pyrolysis of Wood/Biomass for Bio-Oil: A Critical Review. Energy Fuels 2006, 20, 848–888. [Google Scholar] [CrossRef]
  33. Qureshi, K.M.; Lup, A.N.K.; Khan, S.; Abnisa, F.; Daud, W.M.A.W. Effect of Temperature and Feed Rate on Pyrolysis Oil Produced via Helical Screw Fluidized Bed Reactor. Korean J. Chem. Eng. 2021, 38, 1797–1809. [Google Scholar] [CrossRef]
  34. Suman, S.; Gautam, S. Effect of Pyrolysis Time and Temperature on the Characterization of Biochars Derived from Biomass. Energy Sources Part A Recovery Util. Environ. Eff. 2017, 39, 933–940. [Google Scholar] [CrossRef]
  35. American Standard Technical Material–ASTM D 1102-84; Standard Test Method for Ash in Wood by Celebrating 125 Years. ASTM International: West Conshohocken, PA, USA, 2021.
  36. American Standard Technical Material–ASTM D 2016-74; Methods of Test for Moisture Content of Wood by Celebrating 125 Years. ASTM International: West Conshohocken, PA, USA, 1983.
  37. American Standard Technical Material–ASTM D 3178-89; Methods of Test for Carbon and Hydrogen in the Analysis Sample of Coal and Coke by Celebrating 125 Years. ASTM International: West Conshohocken, PA, USA, 2002.
  38. American Standard Technical Material–ASTM D 3175-07; Standard Specification for Pyrolysis Liquid Biofuel by Celebrating 125 Years. ASTM International: West Conshohocken, PA, USA, 2017.
  39. Demirbas, A.; Ak, N.; Aslan, A.; Sen, N. Calculation of Higher Heating Values of Hydrocarbon Compounds and Fatty Acids. Pet. Sci. Technol. 2018, 36, 712–717. [Google Scholar] [CrossRef]
  40. Acar, S.; Ayanoglu, A. Determination of Higher Heating Values (HHVs) of Biomass Fuels. Energy Educ. Sci. Technol. Part A Energy Sci. Res. 2012, 28, 749–758. [Google Scholar]
  41. Noushabadi, A.S.; Dashti, A.; Ahmadijokani, F.; Hu, J.; Mohammadi, A.H. Estimation of Higher Heating Values (HHVs) of Biomass Fuels Based on Ultimate Analysis Using Machine Learning Techniques and Improved Equation. Renew. Energy 2021, 179, 550–562. [Google Scholar] [CrossRef]
  42. Sukumar, V.; Manieniyan, V.; Senthilkumar, R.; Sivaprakasam, S. Production of Bio Oil from Sweet Lime Empty Fruit Bunch by Pyrolysis. Renew. Energy 2020, 146, 309–315. [Google Scholar] [CrossRef]
  43. Rezaei, P.S.; Shafaghat, H.; Daud, W.M.A.W. Production of Green Aromatics and Olefins by Catalytic Cracking of Oxygenate Compounds Derived from Biomass Pyrolysis: A Review. Appl. Catal. A Gen. 2014, 469, 490–511. [Google Scholar] [CrossRef]
  44. Younis, M.R.; Farooq, M.; Imran, M.; Kazim, A.H.; Shabbir, A. Characterization of the Viscosity of Bio-Oil Produced by Fast Pyrolysis of the Wheat Straw. Energy Sources Part A Recovery Util. Environ. Eff. 2021, 43, 1853–1868. [Google Scholar] [CrossRef]
  45. Paenpong, C.; Pattiya, A. Effect of Pyrolysis and Moving-Bed Granular Filter Temperatures on the Yield and Properties of Bio-Oil from Fast Pyrolysis of Biomass. J. Anal. Appl. Pyrolysis 2016, 119, 40–51. [Google Scholar] [CrossRef]
  46. American Standard Technical Material–ASTM D 240-19; Standard Test Method for Heat of Combustion of Liquid Hydrocarbon Fuels by Bomb Calorimeter by Celebrating 125 Years. ASTM International: West Conshohocken, PA, USA, 2019.
  47. Sakulkit, P.; Palamanit, A.; Dejchanchaiwong, R.; Reubroycharoen, P. Characteristics of Pyrolysis Products from Pyrolysis and Co-Pyrolysis of Rubber Wood and Oil Palm Trunk Biomass for Biofuel and Value-Added Applications. J. Environ. Chem. Eng. 2020, 8, 104561. [Google Scholar] [CrossRef]
  48. Geng, A. Upgrading of Oil Palm Biomass to Value-Added Products. In Biomass and Bioenergy: Applications; Springer: Cham, Switerland, 2015. [Google Scholar]
  49. Pimenidou, P.; Dupont, V. Characterisation of Palm Empty Fruit Bunch (PEFB) and Pinewood Bio-Oils and Kinetics of Their Thermal Degradation. Bioresour. Technol. 2012, 109, 198–205. [Google Scholar] [CrossRef]
  50. Dhyani, V.; Bhaskar, T. A Comprehensive Review on the Pyrolysis of Lignocellulosic Biomass. Renew. Energy 2018, 129, 695–716. [Google Scholar] [CrossRef]
  51. Khongphakdi, P.; Palamanit, A.; Phusunti, N.; Tirawanichakul, Y.; Shrivastava, P. Evaluation of Oil Palm Biomass Potential for Bio-Oil Production via Pyrolysis Processes. Int. J. Integr. Eng. 2020, 12, 226–233. [Google Scholar]
  52. Kumar, R.; Strezov, V. Thermochemical Production of Bio-Oil: A Review of Downstream Processing Technologies for Bio-Oil Upgrading, Production of Hydrogen and High Value-Added Products. Renew. Sustain. Energy Rev. 2021, 135, 110152. [Google Scholar] [CrossRef]
  53. Qureshi, K.M.; Kay Lup, A.N.; Khan, S.; Abnisa, F.; Wan Daud, W.M.A. Optimization of Palm Shell Pyrolysis Parameters in Helical Screw Fluidized Bed Reactor: Effect of Particle Size, Pyrolysis Time and Vapor Residence Time. Clean. Eng. Technol. 2021, 4, 100174. [Google Scholar] [CrossRef]
  54. Maulinda, L.; Husin, H.; Rahman, N.A.; Rosnelly, C.M.; Nasution, F.; Abidin, N.Z.; Faisal; Yani, F.T.; Ahmadi. Effects of Temperature and Times on the Product Distribution of Bio-Oils Derived from Typha Latifolia Pyrolysis as Renewable Energy. Results Eng. 2023, 18, 101163. [Google Scholar] [CrossRef]
  55. Chorazy, T.; Čáslavský, J.; Žvaková, V.; Raček, J.; Hlavínek, P. Characteristics of Pyrolysis Oil as Renewable Source of Chemical Materials and Alternative Fuel from the Sewage Sludge Treatment. Waste Biomass Valorization 2020, 11, 4491–4505. [Google Scholar] [CrossRef]
  56. Mansor, A.M.; Lim, J.S.; Ani, F.N.; Hashim, H.; Ho, W.S. Characteristics of Cellulose, Hemicellulose and Lignin of MD2 Pineapple Biomass. Chem. Eng. Trans. 2019, 72, 79–84. [Google Scholar] [CrossRef]
  57. Cai, W.; Dai, L.; Liu, R. Catalytic Fast Pyrolysis of Rice Husk for Bio-Oil Production. Energy 2018, 154, 477–487. [Google Scholar] [CrossRef]
  58. Kan, T.; Strezov, V.; Evans, T.J. Lignocellulosic Biomass Pyrolysis: A Review of Product Properties and Effects of Pyrolysis Parameters. Renew. Sustain. Energy Rev. 2016, 57, 1126–1140. [Google Scholar] [CrossRef]
  59. Palamanit, A.; Khongphakdi, P.; Tirawanichakul, Y.; Phusunti, N. Investigation of Yields and Qualities of Pyrolysis Products Obtained from Oil Palm Biomass Using an Agitated Bed Pyrolysis Reactor. Biofuel Res. J. 2019, 6, 1065–1079. [Google Scholar] [CrossRef]
  60. Chukwuneke, J.L.; Ewulonu, M.C.; Chukwujike, I.C.; Okolie, P.C. Physico-Chemical Analysis of Pyrolyzed Bio-Oil from Swietenia Macrophylla (Mahogany) Wood. Heliyon 2019, 5, e01790. [Google Scholar] [CrossRef] [PubMed]
  61. Nandiyanto, A.B.D.; Oktiani, R.; Ragadhita, R. How to Read and Interpret Ftir Spectroscope of Organic Material. Indones. J. Sci. Technol. 2019, 4, 97–118. [Google Scholar] [CrossRef]
  62. Pinto, O.; Romero, R.; Carrier, M.; Appelt, J.; Segura, C. Fast Pyrolysis of Tannins from Pine Bark as a Renewable Source of Catechols. J. Anal. Appl. Pyrolysis 2018, 136, 69–76. [Google Scholar] [CrossRef]
  63. Adegoke, I.A.; Ogunsanwo, O.Y.; Ige, A.R. Bio-Fuel Properties and Elemental Analysis of Bio-Oil Produced from Pyrolysis of Gmelina Arborea. Acta Chem. Malays. 2021, 5, 38–41. [Google Scholar] [CrossRef]
  64. Zhao, Z.; Jiang, Z.; Xu, H.; Yan, K. Selective Production of Phenol-Rich Bio-Oil From Corn Straw Waste by Direct Microwave Pyrolysis Without Extra Catalyst. Front. Chem. 2021, 9, 700887. [Google Scholar] [CrossRef] [PubMed]
  65. Mullen, C.A.; Boateng, A.A. Chemical Composition of Bio-Oils Produced by Fast Pyrolysis of Two Energy Crops. Energy Fuels 2008, 22, 2104–2109. [Google Scholar] [CrossRef]
  66. Alvarez, J.; Lopez, G.; Amutio, M.; Bilbao, J.; Olazar, M. Bio-Oil Production from Rice Husk Fast Pyrolysis in a Conical Spouted Bed Reactor. Fuel 2014, 128, 162–169. [Google Scholar] [CrossRef]
  67. Lazzari, E.; dos Santos Polidoro, A.; Onorevoli, B.; Schena, T.; Silva, A.N.; Scapin, E.; Jacques, R.A.; Caramão, E.B. Production of Rice Husk Bio-Oil and Comprehensive Characterization (Qualitative and Quantitative) by HPLC/PDA and GC × GC/QMS. Renew. Energy 2019, 135, 554–565. [Google Scholar] [CrossRef]
Figure 1. Schematic illustration of the pyrolysis of Mimusops elengi.
Figure 1. Schematic illustration of the pyrolysis of Mimusops elengi.
Sustainability 15 13851 g001
Figure 2. Thermogravimetric analysis of Mimusops elengi relative to (a) temperature and (b) time.
Figure 2. Thermogravimetric analysis of Mimusops elengi relative to (a) temperature and (b) time.
Sustainability 15 13851 g002
Figure 3. Pyrolysis yield of Mimusops elengi; (a) the influence of pyrolysis temperature; (b) the influence of pyrolysis time.
Figure 3. Pyrolysis yield of Mimusops elengi; (a) the influence of pyrolysis temperature; (b) the influence of pyrolysis time.
Sustainability 15 13851 g003
Figure 4. Bio-oil from pyrolysis of Mimusops elengi.
Figure 4. Bio-oil from pyrolysis of Mimusops elengi.
Sustainability 15 13851 g004
Figure 5. FT-IR spectra of the bio-oil from Mimusops elengi; (a) FT-IR spectra of bio-oil at different temperatures; (b) FT-IR spectra of bio-oil at different times.
Figure 5. FT-IR spectra of the bio-oil from Mimusops elengi; (a) FT-IR spectra of bio-oil at different temperatures; (b) FT-IR spectra of bio-oil at different times.
Sustainability 15 13851 g005
Figure 6. GC-MS spectra of bio-oils from Mimusops elengi at optimal temperature and time (T = 500 °C and t = 90 min).
Figure 6. GC-MS spectra of bio-oils from Mimusops elengi at optimal temperature and time (T = 500 °C and t = 90 min).
Sustainability 15 13851 g006
Table 1. The proximate and ultimate analyses of Mimusops elengi.
Table 1. The proximate and ultimate analyses of Mimusops elengi.
Characteristics Value
Proximate Analysis (wt%)
Moisture content 12.00
Volatile matter 62.35
Fixed carbon 21.16
Ash 5.49
HHV (MJ/kg)18.886
LHV (MJ/kg)16.41
Ultimate Analysis (wt%)
C45.91
H 6.42
O40.28
N1.64
S0.26
Component Analysis (wt%) [17]
Cellulose33.17
Hemicellulose-
Lignin10.2
Others-
Table 2. Characteristics of bio-oil (ASTM 7544-12) [38].
Table 2. Characteristics of bio-oil (ASTM 7544-12) [38].
PropertyTest MethodSpecificationUnits
Density at 20 °CD40521.1–1.3kg/m3
Kinematic viscosity at 40 °CD445125 maxcSt
pHE70-07report
Table 3. Physical properties of bio-oil from Mimusops elengi.
Table 3. Physical properties of bio-oil from Mimusops elengi.
Operating ConditionsDensity (kg/m3)
@20 °C
Viscosity (cSt)
@40 °C
pHHHV (MJ/Kg)
a Temperature (°C)
3001.12 ± 0.0261.31 ± 0.0364.00 ± 0.05316.80 ± 0.062
3501.13 ± 0.0261.32 ± 0.0264.11 ± 0.06117.44 ± 0.087
4001.13 ± 0.0261.40 ± 0.0364.12 ± 0.04317.59 ± 0.124
4501.13 ± 0.0431.42 ± 0.0364.22 ± 0.07818.14 ± 0.213
5001.15 ± 0.0431.60 ± 0.0624.41 ± 0.04619.91 ± 0.081
b Reaction time (min)
301.13 ± 0.0611.56 ± 0.0884.06 ± 0.11119.77 ± 0.121
601.13 ± 0.0701.37 ± 0.0924.00 ± 0.05516.76 ± 0.079
901.15 ± 0.0781.60 ± 0.0264.41 ± 0.05318.14 ± 0.141
1201.15 ± 0.0261.44 ± 0.0704.33 ± 0.06119.42 ± 0.026
a Mimusops elengi pyrolysis at 90 min. b Mimusops elengi pyrolysis at 500 °C.
Table 4. FT-IR results and functional group compositions of the bio-oil.
Table 4. FT-IR results and functional group compositions of the bio-oil.
Absorption
(cm−1)
Wavenumber (cm−1)Type of VibrationsClass of Compounds
a Reaction Time (min)b Temperature (°C)
306090120300350400450500
3584–3700--3699369936993699369936993699O-H stretchAlcohols
--3390-----3390
3300–34003379---3379----O-H stretchAlcohols
3377-3377-337733773377-
2850–30002900--------C-H stretchAlkanes
-2891-------
--2889288928892889288928892889
2815–2850-2835-------C-H stretchEsters
----2833283328332833-
----2382----
-------2380-
2300–2400-2376----2376--C≡NNitrile stretch
--2349-----2349
---234723472347---
2100–2140-2119-------C≡CAlkynes
2112----2112-2112-
---2100--2100--
1660–2000--1867-----1867Aromatic combination bandsAromatic
-------1865-
C=O stretchAldehydes
-1766-1766176617661766-- ketones
1700–1790-------1764-
1762--------
--1708-----1708C=C stretchAlkenes
-------1647-
1620–1680--16431643164316431643-1643
1641--------C-H blendAromatics
-1637-------
1450–1600-----1566-1566-
---15601560-1560--
15161516-15161516151615161516-
--1514-----1514
----14521452---C-HAlkenes
-------1450-
1410–1420---1413-14131413--O-H blendAlcohols
-------1411-
1310–14101409--------
-1404-------
-- -1402----O=C-O-CEsters
--1370-----1370 (aromatics)
1250–1310---12761276127612761276-
12741274-------C-O stretchAlcohols
--1271-----1271
1035–1085--1082-----1082
--1051-----1051
-1049-------
1047---1047-10471047-
990–10501016-10161016--101610161016P-O-C stretchPhosphorus
----10141014---
610–700680680680680680680680680680≡C-H stretchAlkynes
607607607607607607607607607
a Mimusops elengi pyrolysis at 500 °C. b Mimusops elengi pyrolysis at 90 min.
Table 5. Concentrations of some compounds in Mimusops elengi bio-oil from pyrolysis.
Table 5. Concentrations of some compounds in Mimusops elengi bio-oil from pyrolysis.
NoCompoundFormulaArea (%)Groups
1Phosphonic acidC6H7O4P4.89Acid
22-cyclopentene-1-one, 2-hydroxy-3-methylC6H8O20.97Ketone
3Oxiranecarboxamide, 2-ethyl-3-propylC8H15NO24.31Acid
4p-cresolC7H8O1.73Phenol
51,2,3-Propanetriol, 1-acetateC5H10O41.37Acid
63-pyridinolC5H5NO2.01Aromatic
7GlutarimideC5H7NO22.22Acid
8GuanosineC10H13N5O51.26Acid
91,4;3,6-Dianhydro-alpha-d-glucopyranoseC6H8O40.93Hydrocarbon
101,4;3,6-Dianhydro-alpha-d-glucopyranoseC6H8O47.02Hydrocarbon
113,4-Anhydro-d-galactosanC6H8O41.09Ester
12CatecholC6H6O236.63Phenol
135H-CyclopentapyrazineC9H12N22.47Pyrazine
142-Butanone, 4-hydroxy-3,3-dimethylC6H12O20.93Ester
151,2-Benzenediol, 3-methoxyC7H8O33.31Phenol
161,2-Benzenediol, 3-methylC7H8O23.85Phenol
171,4-BenzenediolC6H6O25.61Phenol
18Beta-d-Ribopyranoside, methyl, 3-acetateC8H14O61.29Ester
191,2-Benzenediol, 4-methylC7H8O26.46Phenol
20PhenolC8H10O32.35Phenol
214,6-Dimethyl (1H) pyrid-2-oneC14H13N3O32.99Ketone
221,4-Benzenediol, 2,6-dimethylC8H10O21.05Phenol
231,3-Benzenediol, 4-ethylC8H10O21.59Phenol
242,5-Dimethoxybenzyl alcoholC9H12O30.38Alcohol
25D-AlloseC6H12O61.65Hydrocarbon
264-Oxo-beta-isodamascolC13H20O21.66Phenol
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Maulinda, L.; Husin, H.; Arahman, N.; Rosnelly, C.M.; Syukri, M.; Nurhazanah; Nasution, F.; Ahmadi. The Influence of Pyrolysis Time and Temperature on the Composition and Properties of Bio-Oil Prepared from Tanjong Leaves (Mimusops elengi). Sustainability 2023, 15, 13851. https://doi.org/10.3390/su151813851

AMA Style

Maulinda L, Husin H, Arahman N, Rosnelly CM, Syukri M, Nurhazanah, Nasution F, Ahmadi. The Influence of Pyrolysis Time and Temperature on the Composition and Properties of Bio-Oil Prepared from Tanjong Leaves (Mimusops elengi). Sustainability. 2023; 15(18):13851. https://doi.org/10.3390/su151813851

Chicago/Turabian Style

Maulinda, Leni, Husni Husin, Nasrul Arahman, Cut Meurah Rosnelly, Muhammad Syukri, Nurhazanah, Fahrizal Nasution, and Ahmadi. 2023. "The Influence of Pyrolysis Time and Temperature on the Composition and Properties of Bio-Oil Prepared from Tanjong Leaves (Mimusops elengi)" Sustainability 15, no. 18: 13851. https://doi.org/10.3390/su151813851

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop