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Review

Production of Biofuels from Glycerol from the Biodiesel Production Process—A Brief Review

by
Eugênia Leandro Almeida
,
José Eduardo Olivo
and
Cid Marcos Gonçalves Andrade
*
Department of Chemical Engineering, State University of Maringá, Av. Colombo 5790, Maringá 87020-900, Brazil
*
Author to whom correspondence should be addressed.
Fermentation 2023, 9(10), 869; https://doi.org/10.3390/fermentation9100869
Submission received: 2 August 2023 / Revised: 18 September 2023 / Accepted: 20 September 2023 / Published: 27 September 2023

Abstract

:
Biodiesel is seen as a successor to diesel of petrochemical origin, as it can be used in cycle and stationary engines and be obtained from renewable raw materials. Currently, the biodiesel production process on an industrial scale is mostly carried out through the transesterification reaction, also forming glycerol as a product. Pure glycerol is used in the pharmaceutical, cosmetic, cleaning, food, and other industries. Even presenting numerous applications, studies indicate that there is a saturation of glycerol in the market, which is directly related to the production of biodiesel. This increase causes a commercial devaluation of pure glycerol, making separation and purification processes unfeasible from an economic point of view. Despite the economic unfeasibility of the aforementioned processes, they continue to be carried out due to environmental issues. Faced with the problem presented, this work provides a bibliographical review of works that aimed to use glycerol as a raw material for the production of biofuels, with these processes being carried out mostly via fermentation.

1. Introduction

Currently, biodiesel stands out as a successor to diesel of petrochemical origin since there is worldwide concern about the depletion of fossil fuels as well as the emission of gases produced from their burning, gases that contribute to the aggravation of the greenhouse effect [1,2]. Biodiesel, like diesel, can be used in cycle and stationary engines [3]. The use of biodiesel has some advantages, such as being obtained from renewable sources and a lower rate of emission of gases that contribute to the worsening of the greenhouse effect [4,5].
Biodiesel on an industrial scale is mostly produced through the methyl transesterification reaction using basic homogeneous catalysts, such as sodium and potassium hydroxides [6,7,8], and can be obtained from different raw materials, e.g., vegetable oils and animal fats [9,10].
During the biodiesel production process via transesterification, there is also the formation of glycerol [4,11]. It is estimated that for every 10 kg of biodiesel produced, approximately 1 kg of crude glycerol is formed [12,13]. For the commercialization of glycerol produced from the biodiesel production process, crude glycerol is subjected to separation and purification processes, thus obtaining pure glycerol [14].
Pure glycerol is used in the food industry as a stabilizer, antioxidant, humectant, and emulsifier; in the pharmaceutical industry in cosmetics and medicines; and in the chemical industry in the composition of resins and polymers, among other uses [15,16]. Despite being used in several industrial sectors, the market is saturated with this product, as the demand for glycerol is less than the quantity produced, causing the commercial devaluation of glycerol [17]. According to Zhang et al. (2016), the energy expenditure during the separation and purification processes is unfeasible due to the low economic value attributed to purified glycerol, which is associated with the growing amount of glycerol in the market due to the production of biodiesel [18].
It is important to point out that although the separation and purification processes are impracticable, they are necessary since crude glycerol without treatment cannot be discarded in the environment and its use as fuel is unfeasible because its direct burning produces toxic gases [14].
As already mentioned, biodiesel is a potential successor to diesel, which is a reality in many countries. The biodiesel production process via the transesterification reaction is the most used, and during this process there is the production of glycerol, currently considered a by-product [19,20]. The considerable increase in the amount of glycerol in the market, according to studies, is directly associated with the production of biodiesel [21,22]. This increase in the amount of glycerol in the market has caused a devaluation of its commercial value, making separation and purification processes energetically and economically unfeasible [18]. Therefore, proposing the use of glycerol as a renewable raw material for the production of other biofuels is interesting from an economic, energy, and technological development point of view. It is an attempt to value this by-product that has saturated the market. In this way, considering the current scenario, including seeking the development of new forms of biofuel and the whole problem presented in relation to the biodiesel production process and glycerol, this review aims to present works that had the production of other biofuels as their objective, including methane, hydrogen, and ethanol, via fermentation processes using glycerol from biodiesel production as the raw material. It is important to highlight that this work aimed to carry out a review with a focus on fermentation because it is a more economically viable route, since it makes it possible to use crude glycerol as a source of raw material. We did not find a review in the consulted literature that performed this task, and it is thus our main contribution.

2. Glycerol

The official name of glycerol, according to IUPAC (International Union of Pure and Applied Chemistry), is propane-1,2,3-triol. The molecular formula of glycerol is C3H5(OH)3. Glycerol is a colorless liquid, has an oily appearance, is viscous, has a relatively high density, is soluble in water and alcohols, and is practically insoluble in hydrocarbons [23,24]. Table 1 presents the physicochemical properties of glycerol.
As shown in Table 1, the decomposition point of glycerol is 290 °C. According to Gupta et al. (2012), it is at this temperature that the decomposition of glycerol into acrolein, a toxic and carcinogenic compound, occurs [14].
Glycerol can be obtained from sources considered renewable, including vegetable oils and animal fats, and also from sources considered non-renewable, such as petroleum. Glycerol can be obtained from fermentation processes, chemical processes such as the hydrogenation of carbohydrates of petrochemical origin, the saponification process, and the biodiesel production process. The physicochemical properties of glycerol may vary depending on the raw material used. The work carried out by Quispe et al. (2013) showed that when using different vegetable oils as the raw materials, the formed glycerol had different viscosities [25].
Glycerol from the biodiesel production process is mostly obtained through the transesterification reaction [26,27]. The transesterification reaction is represented in Figure 1.
The transesterification reaction is a reversible reaction, so it is necessary to add one of the reagents in excess; in this case, it is common to add alcohol in excess [28,29]. The alcohols frequently used are methanol and ethanol, with methanol being the most used since the use of ethanol in the production process requires a greater excess of product, presenting a greater propensity to form soaps and forming an emulsion that makes the processes of separation and purification difficult, in addition to the relatively higher commercial price when compared to methanol [30,31]. The catalysts frequently used on an industrial scale are homogeneous alkaline catalysts, especially sodium and potassium hydroxides [32]. The use of these catalysts has some advantages, such as lower economic cost, shorter reaction time, higher conversion rates, etc. However, these same catalysts have disadvantages, such as the need for a raw material with a low fatty acid content, since these catalysts in the presence of fatty acids and alcohol favor the formation of soaps [6,8,33,34,35,36]. It is important to highlight that there are works available in the literature that proposed the use of other catalysts, such as heterogeneous acid catalysts [20,37]. According to Alcañiz-Monge et al. (2013), heterogeneous acid catalysts have the advantage of obtaining biodiesel both through the esterification of fatty acids and transesterification of triglycerides, forming purer products and allowing possible reuse in a new process [38,39]. However, when compared to conventional catalysis, both heterogeneous and homogeneous acid catalysis have some disadvantages, such as requiring longer reaction time and higher operating costs [40,41].
After the transesterification reaction, the reaction product goes through the separation and purification processes, where the catalyst is neutralized, the alcohol added in excess is recovered, and the purified products are obtained for commercialization [42,43,44]. Figure 2 presents a diagram of the biodiesel and glycerol production process.
The purification process begins with the separation of the light phase, mostly made up of biodiesel, from the heavy phase, mostly made up of glycerol. The heavy phase, as mentioned, comprises mostly glycerol, alcohol, water, catalyst, impurities, soaps, and non-glycerol organic matter. The glycerol purification process begins with the process of neutralizing the catalyst present in the solution, followed by the process of separating the salts formed in the neutralization process, catalyst residues, soaps, and organic material. The resulting solution has a concentration of 40–70% glycerol, which undergoes a vacuum evaporation process in which almost all water and alcohol is removed, and the resulting solution has a concentration greater than or equal to 80% glycerol. The solution, in turn, undergoes a refining process until it reaches the purity level required for commercialization [46,47]. Vacuum distillation is the process often used to obtain purified glycerol [24,46]. Figure 3 presents a simplified diagram of the glycerol separation and purification processes.
Biodiesel and glycerol production is a complex process that demands a high energy expenditure from the preparation of the raw material to obtaining the final products. This reinforces the need to make glycerol an energetically and economically attractive product, consequently increasing the viability of the biodiesel production process on an industrial scale [25].

3. Biofuel Production Processes Using Glycerol as Biomass

The use of glycerol as a carbon source for the production of biofuels has been gaining prominence due to its wide availability [18,48]. Another reason that corroborates the development of research in this area is the physicochemical characteristics of glycerol, such as high autoignition temperature and low heating value, causing glycerol to decompose into acrolein at 290 °C [49]. The following topics present works that aimed to use glycerol as a renewable raw material for the production of fuels.

3.1. Biogas

Recent studies present glycerol as a promising source of organic matter for the production of biogas [50,51,52,53]. In the biogas production process, glycerol can be used as a substrate or co-substrate [54]. Different bacteria are capable of metabolizing glycerol, including those of the genera Klebsiella, Clostridium, and Enterobacter [15,55,56,57].
The work carried out by Astals et al. (2012) aimed to produce biogas from the anaerobic digestion of swine effluents using crude glycerol as a co-substrate. They added 4% w/w, on a wet basis, of crude glycerol to the bioreactor and obtained a 400% increase in biogas production with respect to monodigestion. The authors concluded that the results were satisfactory, and the increase in biogas production may have been due to the increase in organic load, the carbon–nitrogen balance, and the decrease in ammonia concentration [58].
The work carried out by Siles et al. (2010) aimed to use glycerol in the co-digestion of wastewater formed during the biodiesel production process, with the purpose of treating the effluent as well as the production of methane. Some of the main factors evaluated by the authors were: biodegradability of the mixture formed by wastewater and glycerol, methane yield coefficient, and methane production kinetics. The inoculum used was the active methanogenic granular biomass used to treat wastewater from breweries. According to the authors, this biomass was selected due to its high methanogenic activity. Before forming the mixture, which was subsequently treated, the authors carried out the acidification and centrifugation of the glycerol, with the purpose of removing the catalysts used in the transesterification reaction and electrocoagulation process in the wastewater. The authors concluded that the results presented were satisfactory, as the mixture showed a high level of biodegradability, the kinetics of methane production remained constant, and the production of 310 mL of CH4/g was removed at 1 atm and 25 °C [59].
The work carried out by Beschkov et al. (2012) aimed to develop a mathematical model to describe the production of biogas and other products from the anaerobic digestion of crude glycerol using Klebsiella sp. bacteria. Experiments were carried out in a multistage bioreactor, and the results obtained were used to develop the proposed model. The choice of a multistage reactor was directly related to the intermediates formed during the glycerol digestion process, as these intermediates were acidic in character, lowering the pH of the medium and inhibiting the methanogenesis reaction. Thus, the chosen reactor separated the inhibition zone from the methanogenesis zone. The authors concluded that, although simple, the proposed model allowed estimating the number of compartments necessary for the total conversion of glycerol into biogas [60].
The work carried out by Fountoulakis et al. (2009) aimed to verify the influence of adding glycerol in continuous bioreactors that treated small fractions of urban organic waste and wastewater. The authors observed that the methane production rate increased with the addition of crude glycerol. The reactor was inoculated with anaerobic sludge from the municipal sewage treatment plant in the city of Iraklio, Greece. The authors observed the production of 1400 mL CH4/d without adding glycerol and 2094 mL CH4/d after adding glycerol. They concluded that the results were satisfactory [54].
The work carried out by Oliveira (2015) aimed to evaluate the optimal conditions for methane production using macroalgae Sargassum sp. co-digested with glycerol and residual frying oil. The authors noted that without the addition of glycerol and residual oil, the biochemical potential of Sargassum sp. was 181 ± 1 L CH4/L of COD and the methane rate increased 56% with the addition of glycerol and 46% with the addition of residual oil. The authors concluded that the addition of glycerol or residual oil was a promising alternative for methane production [61].
The work carried out by Sittijunda and Reungsang (2018) aimed to verify the methane production from the co-digestion of algae biomass with crude glycerol. The authors showed that under optimal conditions the maximum methane production was 58.88 mL CH4/L. The bacteria detected that were responsible for the digestion of the biomass were Methanosarcina sp., Methanoregula sp., Methanospirillum sp., and Methanoculleus sp. [62].
The work carried out by Baba et al. (2013) aimed to carry out an energy balance in a process plant in which crude glycerol was digested. The results presented, according to the authors, were satisfactory in terms of methane production. According to the analyses carried out, the digested sludge contained fertilizer components (N: 0.11%, P2O5: 0.036%, K2O: 0.19%). Thus, the authors concluded that crude glycerol was an attractive biomass for methane production and the residual sludge could be used as liquid fertilizer [50].
The work carried out by Chou and Su (2019) aimed to evaluate the feasibility of biogas production by anaerobic co-digestion of wastewater from dairy cattle and crude glycerol. The authors concluded that the conversion of residual crude glycerol into biogas showed satisfactory results and could be applied in the near future on an industrial scale to treat waste from slaughterhouses [63].
The work carried out by Sawasdee et al. (2019) aimed to evaluate the production of biogas from the co-digestion of glucose and glycerol in laboratory-scale batch reactors. The experiments involved varying glycerol/glucose ratios with fixed initial chemical oxygen demand for all conditions. The inoculum was obtained from cassava starch sludge. The highest yield of biogas production was obtained using the 5:5 ratio of glycerol/glucose, with a maximum production rate of 8 mL/h [64].
The work carried out by Alves et al. (2020) aimed to evaluate the effect of adding crude glycerol on the anaerobic digestion of primary sewage sludge. Crude glycerol was added in two fractions, 1% and 3% v/v. The methane yields were 223.8 mL CH4/g VS for 1% concentration and 368.8 mL CH4/g VS for 3% concentration, which represented increases in methane yield of 61% and 167% compared to the control test performed only with primary sludge digestion (138.2 mL CH4/g VS). For each percentage increase in applied SV load, the percentage increases in methane yield were 4.7% and 5.7% with 1% and 3% glycerol, respectively [65].
The work carried out by Prasertsan et al. (2021) aimed to evaluate the production of biogas using fluent raw material from a palm oil factory and evaluate which co-substrate had the highest yield, crude glycerol or ethanol. Concentrations of both substrates ranged from 1% to 5% v/v. The optimal concentrations of crude glycerol and ethanol were 1% and 5% v/v, respectively. The results presented by the authors showed that the removal of volatile solids using crude glycerol as a co-substrate presented better performance when compared to ethanol. However, regarding the biogas production rate, the results were the opposite, with a production rate of 553.46 mLCH4/g VS for glycerol and 582.12 mL CH4/g VS for ethanol. The dominant microorganisms were Methanosarcina sp. and Methanospirillum sp. [66].
The work carried out by Takeda et al. (2022) aimed to produce biogas using landfill leachate and crude glycerol as the raw materials. The authors analyzed the following parameters: removal of organic matter, time, glycerol content, and substrate/inoculum ratio. From the optimization of the mentioned parameters it was possible to maximize the efficiency of organic matter removal (90.15%) and specific production of biogas (403.15 mL/g SSV) under the conditions of 33.2 days, glycerol content of 1.71%, and substrate/inoculum ratio of 0.37 g COD/g VSS. The authors concluded that the average specific production of biogas was 20.3 times higher than that obtained by monodigestion of landfill leachate [67].
The work carried out by Bułkowska et al. (2022) aimed to evaluate the effect of glycerol on the anaerobic digestion of bovine manure under mesophilic conditions. The process was carried out in stirred tank semi-continuous reactor at a constant organic rate and hydraulic retention time of 30 days. It was found that the addition of glycerol to cattle manure produced 3.1 times more biogas than that by cattle manure alone (237.5 L vs. 76.4 L) [68].
The work carried out by Alves et al. (2022) evaluated the co-digestion of primary sewage treatment sludge, food waste, and crude glycerol. Crude glycerol concentrations were 1% and 3% v/v. The results presented by the authors were biogas yields of 432.4 and 692.6 mL/g VS for 1% and 3% crude glycerol, respectively, while the methane yields corresponded to 343.3 and 525.7 mL CH4/g VS for 1% and 3% crude glycerol, respectively. The latter represented increases of 45.4% and 122.7% in relation to those achieved with primary sludge and food residues in mixtures [69].
Table 2 summarizes the production of biogas using glycerol as the raw material.

3.2. Hydrogen

Currently, hydrogen is seen as a form of clean energy, since the only product of the combustion process is water [70]. Conventional forms of hydrogen production are catalytic reforming in petroleum processing and steam reforming of methane present in natural gas; however, these methods cannot be considered renewable since both use raw materials of fossil origin [71,72]. Another conventional method used for the production of hydrogen is the electrolysis of water; however, this method demands a high energy cost [70]. Due to the problems involved in conventional methods, the use of glycerol as biomass for the production of hydrogen is an interesting alternative method since it causes less environmental impact and requires less energy expenditure [73,74,75]. The process of producing hydrogen through the fermentation process is mainly carried out by anaerobic digestion, called dark fermentation [76,77]. According to Maru (2016), dark fermentation offers significant advantages when compared to other hydrogen production processes, as it requires less investment, the operating conditions are simpler, and it is environmentally more advantageous [78]. In this process, organic substrates, such as glycerol, are decomposed by hydrogen-producing microorganisms, and methanogenic microorganisms must be eliminated from the process so that they do not produce methane [79,80].
The work carried out by Maru et al. (2016) aimed to produce hydrogen through the fermentation process using pure and residual glycerol as the raw materials. The fermentation process was carried out and compared using three strains, Escherichia coli CECT432, Escherichia coli CECT434, and Enterobacter cloacae MCM2/1. Escherichia coli CECT432 was the strain that obtained the highest hydrogen production using pure glycerol, and a co-culture formed by Escherichia coli CECT432 and Enterobacter cloacae MCM2/1 showed the highest productivity. This same co-culture was used in the fermentation process using residual glycerol, and the results were satisfactory according to the authors. The authors concluded that the strains metabolized residual glycerol without any purification step, and the ability to produce H2 without prior purification of residual glycerol was attractive because it avoided extra costs in the process [78].
The work carried out by Sittijunda and Reungsang (2020) proposed the simultaneous production of hydrogen, ethanol, and 1,3-propanediol. The authors used pure and residual glycerol to convert to desirable products. The process was carried out via fermentation using a co-culture of Enterobacter sp., Klebsiella sp., and Klebsiella pneumoniae. The authors concluded that the use of crude glycerol as the raw material presented satisfactory results [81].
The work carried out by Prakash et al. (2018) aimed to use domestic wastewater and crude glycerol from the biodiesel production process to produce hydrogen via the fermentation process. The cultures used were Bacillus thuringiensis strain EGU4 and Bacillus amyloliquefaciens strain CD16. The results were satisfactory, but when comparing the performance of the two cultures, Bacillus amyloliquefaciens strain CD16 had the highest yield. The authors concluded that the results were satisfactory; however, they emphasized the need for biosafety when working with non-sterile sludge [82].
The work carried out by Chen et al. (2021) aimed to produce hydrogen via the fermentation process using raw glycerol as the raw material and compare the yield of fermentation with immobilized and suspended microorganisms. The inoculum used was collected at a wastewater treatment plant in Beijing, China, pre-treatment with ionizing radiation was performed in order to eliminate hydrogen-consuming bacteria, and the predominant bacterium in the culture was Clostridium sp. The results presented by the authors showed greater yield by fermentation using immobilized microorganisms as well as greater tolerance to the substrate [83].
The work carried out by Silva et al. (2020) aimed to use semi-continuous reactors for the production of hydrogen and volatile fatty acids via a fermentation process, using residual glycerol as a substrate. The microorganisms used were bacteria of the genera Enterobacter and Clostridium. The reactor that operated using bacteria of the genus Clostridium showed lower performance. The authors concluded that the yields found for the production of hydrogen using a semi-continuous reactor via a fermentation process with bacteria of the genus Enterobacter were satisfactory and consistent with the literature [84].
The work carried out by Mirzoyan et al. (2019) aimed to use a mixture of lactose and glycerol for the production of hydrogen via a fermentation process using the bacterium Escherichia coli at different pH values and concentrations. The authors concluded that the results were satisfactory and an alternative for the production of renewable hydrogen [85].
The work carried out by Toledo-Alarcon et al. (2020) aimed to produce hydrogen using glycerol as a substrate and verify the impact of sludge pre-treatment on the production process. Two types of inoculum were used, aerobic and anaerobic sludge, and two types of pre-treatment, aeration and thermal shock. Bacteria of the genus Clostridium were detected as dominant in all inocula. The best results were obtained using anaerobic sludge with thermal pre-treatment [86].
Table 3 summarizes the production of hydrogen using glycerol as the raw material.

3.3. Ethanol

Ethanol is mostly produced from renewable raw materials, especially from sugarcane and corn [87,88,89]. But, according to the study carried out by Yazdani and González (2007), the cost of producing ethanol from glycerol is almost 40% lower than that of ethanol produced from corn, taking into account the demand for raw materials and operational costs [90]. Currently, the ethanol production process using glycerol as a raw material is not considered economically viable when compared to other conventional processes [91,92]. However, the use of glycerol from the biodiesel production process is interesting because of some factors, such as making glycerol a source of biomass and producing ethanol from it, which is one of the alcohols that can be used in the biodiesel production process. This would encourage the development of integrated biorefineries (industrial symbiosis) [93,94] as well as the development of new methods and technologies that may be technically and economically viable in the future [95,96].
The work carried out by Sunarno et al. (2019) aimed to produce ethanol from crude glycerol using Enterobacter aerogenes TISTR 1468 supplemented with a cheaply available nutrient substrate, in this case, tuna condensate. The authors aimed to find the optimal conditions for the concentration of crude glycerol, tuna condensate, inorganic salts, and pH. The optimal conditions for ethanol production were 20 g/L of crude glycerol with the pH maintained at 7, yielding 12.33 g/L [97].
The work carried out by Oh et al. (2011) aimed to produce ethanol using glycerol as a carbon source. A mutant strain was used in the process, Klebsiella pneumoniae GEM167, which was obtained by irradiation. According to the authors, when comparing production with the control strain, an increase in ethanol production was expressly noticeable when using the mutant strain. The maximum production level was 21.5 g/L, with a productivity of 0.93 g/L/h [98].
The work carried out by Stepanov and Efremenko (2017) aimed to develop and use a biocatalyst in the form of a cryogel immobilizing cells of the yeast Pachysolen tannophilus to convert glycerol into ethanol in both batch and continuous modes. According to the authors, the conversion of glycerol into ethanol using this biocatalyst resulted in a yield of 90% in relation to the theoretical limit [99].
The work carried out by Sunarno et al. (2020) aimed to produce ethanol from crude glycerol using Enterobacter aerogenes TISTR 1468. The authors evaluated the conversion of glycerol into ethanol under aerobic and anaerobic conditions. The evaluation was carried out in a reactor with aeration in continuous and batch processes, and the conversion process without aeration was also evaluated. The aeration rate was controlled using the redox potential (OPR). The results presented by the authors showed that in the fermentation process without aeration, the ethanol yield was 18.78 g/L; with aeration, it was 30.31 g/L in the continuous process and 12.33 g/L in the batch process [100].
The work carried out by Suzuki et al. (2015) aimed to produce ethanol using glycerol from the development of a highly ethanol-tolerant Klebsiella variicola mutant, as well as improving the mutant’s ethanol production by optimizing the culture conditions. The mutant obtained from Klebsiella variicola TB-83, called TB-83D, was modified by means of ribosome engineering, and it was more resistant to streptomycin and tolerant to ethanol. The results indicated that the mutant strain showed higher ethanol production [101].
The work carried out by Vikromvarasiri et al. (2016) used an anaerobic sludge blanket reactor for wastewater treatment to test the possibility of producing ethanol in the fermentation process using glycerol as a co-substrate at various glycerol concentrations. The ethanol concentration and yield were highly dependent on the initial glycerol concentration. The highest ethanol concentration was 11.1 g/L obtained after 72 h of fermentation at an initial concentration of 45 g/L of glycerol. The main ethanol producers were identified as Enterobacter and Klebsiella strains [102].
The work carried out by Lee et al. (2017) aimed to convert glycerol into ethanol with Enterobacter aerogenes ATCC 29007 immobilized using alginate. The fermentation process was carried out in a continuous stirred tank reactor (CSTR) designed for continuous production with immobilized cells. The experiments were performed using pure and crude glycerol. Under optimal conditions, the ethanol production and yield were approximately 5.38 g/L and 0.96 mol ethanol/mol glycerol with pure glycerol, respectively, while the ethanol production and yield were approximately 5.29 g/L and 0.91 mol ethanol/mol glycerol with crude glycerol, respectively [103].
Table 4 summarizes the ethanol production using glycerol as the raw material.

4. Considerations

Biodiesel production is a complex process that demands high energy and economic expenditure [104,105]. Therefore, it is important for the industrial viability of biodiesel production to add economic value to glycerol, making glycerol a useful product and not an undesirable by-product [25,106,107].
The production of methane from glycerol is a sustainable alternative to methane extracted from natural gas [108]. Methane production is directly related to biogas production, and it is important to detect which other gases are present in this biogas in order to propose a treatment for its purification as well as the degree of purity of methane [108].
Hydrogen is a promising alternative to fossil fuels because it has a high energy yield (122 kJ/g) and its combustion product is water instead of gases that contribute to the worsening of the greenhouse effect [109]. Hydrogen produced through catalytic cracking of petroleum or through steam reforming of methane present in natural gas cannot be considered a renewable alternative since it is obtained from fossil fuels [110]. The production of hydrogen through water electrolysis demands a high energy cost, making the process unfeasible from an economic point of view. Thus, the fermentation pathway using glycerol as biomass can be attractive both from an environmental and economic point of view for the production of hydrogen [111,112,113].
Currently, ethanol is produced predominantly from sugarcane and corn [114,115,116,117]. However, producing ethanol from glycerol, which is currently seen as a by-product of the biodiesel production process, is a way of adding economic value to glycerol [35,118]. Another perspective is the use of ethanol produced from glycerol returns it to the biodiesel production process as one of the reagents [119].
Another alcohol that can be returned to the process is methanol, which in turn can be obtained from the biogas produced from glycerol, requiring biogas purification processes [120]. The work carried out by Magalhães et al. (2004) proposed the purification of biogas using a packing column and water as the solvent at pressures between 6 and 12 bar [121]. After purifying the biogas, methane underwent an oxidation process in order to obtain synthesis gas, and catalytic reform was employed to obtain methanol [122,123]. The proposal to use biogas to produce methanol is a way to obtain alcohol from a renewable source, since the methanol produced in the current context is predominantly from natural gas of fossil origin [124,125]. And, the methanol produced by this route can be returned to the biodiesel production process plant and for use as one of the reagents [62,126].
Finally, it is important to highlight that production is mostly carried out through biochemical processes; therefore, it is important that the residues from these processes receive adequate microbiological treatment for biosafety reasons [127]. The biofuels reported in these works can be applied in different industrial sectors, and according to the authors, they are attractive alternatives for the use of glycerol as a raw material.

5. Conclusions

The biodiesel production process is complex, demanding a high energy expenditure and consequently having a high economic cost, thereby reinforcing the need to make glycerol an attractive product energetically and economically. Thus, we can conclude that the works presented are alternatives to make the biodiesel production process viable since they sought to use glycerol as a raw material for the production of other biofuels.

Author Contributions

Conceptualization, E.L.A. and C.M.G.A.; formal analysis, E.L.A., J.E.O. and C.M.G.A.; writing—preparation of the original draft, E.L.A.; writing—review and editing, E.L.A. and C.M.G.A.; supervision, J.E.O. and C.M.G.A.; project administration, E.L.A., J.E.O. and C.M.G.A.; acquisition of financing, J.E.O. and C.M.G.A. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Data Availability Statement

Not applicable.

Acknowledgments

The authors wish to thank the Coordination for the Improvement of Higher Education Personnel (CAPES) and National Council for Scientific and Technological Development (CNPq).

Conflicts of Interest

The authors declare no conflict of interest.

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Figure 1. Representation of the transesterification reaction adapted from the work by Almeida et al. (2018) [20].
Figure 1. Representation of the transesterification reaction adapted from the work by Almeida et al. (2018) [20].
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Figure 2. Diagram of the biodiesel and glycerol production process adapted from Almeida et al. (2017) [45].
Figure 2. Diagram of the biodiesel and glycerol production process adapted from Almeida et al. (2017) [45].
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Figure 3. Simplified diagram of the separation and purification processes of glycerol adapted from Luo et al. (2016) [46].
Figure 3. Simplified diagram of the separation and purification processes of glycerol adapted from Luo et al. (2016) [46].
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Table 1. Physicochemical properties of glycerol.
Table 1. Physicochemical properties of glycerol.
PropertyValue
Molecular weight92.09 g/mol
Density at 20 °C1.261 g/cm3
Viscosity at 20 °C1499 cP
Specific heat at 26 °C2.42 J/g
Heat of formation159.6 Kcal/g mol
Heat of combustion1662 KJ/mol
Heat of fusion18.3 KJ/mol
Fusion point17.8 °C
Flash point177 °C
Point of combustion204 °C
Point of decomposition290 °C
Adapted from Gupta et al. (2012) and Mendes et al. (2011) [14,24].
Table 2. Production of biogas using glycerol as the raw material.
Table 2. Production of biogas using glycerol as the raw material.
AuthorsFeedstockMicroorganismTimeTemperaturepHResults
Fountoulakis et al. (2009) [54]Urban effluent and crude glycerolThe inoculum was obtained from anaerobic sludge from a municipal station46 days35 °C7.0–7.5The authors observed the production of 1400 mL CH4/d without adding glycerol and 2094 mL CH4/d after adding glycerol
Astals et al. (2012) [58]Swine effluent and crude glycerolPig manure was used as inoculum20 days6.5The best yield was obtained with 4% crude glycerol added to the bioreactor, obtaining a 400% increase in biogas production with respect to monodigestion
Siles et al. (2010) [59]Crude glycerol and wastewater from the biodiesel production processActive methanogenic granular biomass37 °C7.38Maximum production was 310 mL of CH4/g organic matter removed
Beschkov et al. (2012) [60]Crude glycerolKlebsiella sp.32 °C7.5The authors carried out modeling of a multistage biodigester. From this modeling, it was possible to estimate the number of stages necessary so that one stage does not inhibit another
Oliveira (2015) [61]Crude glycerol and residual frying oilSargassum sp.42 days37 °C7.0–7.4Without the addition of glycerol and residual oil, the biochemical potential of Sargassum sp. was 181 ± 1 L CH4/L of DOC. The methane rate increased 56% with the addition of glycerol and 46% with the addition of residual oil
Sawasdee et al. (2019) [64]Glucose and glycerolThe inoculum was obtained from cassava starch sludge37 °C6.63–7.04The highest yield of biogas production was for the 5:5 ratio of glycerol/glucose, with a maximum production rate of 8 mL/h
Alves et al. (2020) [65]Crude glycerol and primary sewage sludgeThe inoculum was obtained from primary sewage sludge20 days37 °C7.55–7.48The methane yields were 223.8 mL CH4/g VS for 1% glycerol concentration and 368.8 mL CH4/g VS for 3% glycerol concentration when crude glycerol was added
Prasertsan et al. (2021) [66]Palm oil factory effluent, crude glycerol and ethanol as co-substratesMethanosarcina sp. and Methanospirillum sp.45 days37 °C6.8–7.4The optimal concentrations for both substrates were 1% for glycerol and 5% for ethanol. The results showed a production rate of 553.46 mLCH4/g VS for glycerol and 582.12 mLCH4/g VS for ethanol
Takeda et al. (2022) [67]Landfill leachate and crude glycerolThe inoculum was obtained from municipal wastewater33 days37 °C7.0Under optimal conditions, biogas production was 403.15 mL/g VSS
Bułkowska et al. (2022) [68]Crude glycerolThe inoculum was obtained from bovine manure30 days39 °C7.47–7.49Adding 10% v/v of glycerol VS increased the methane production rate from 0.295 to 0.844 L/L day and the yield coefficient from 0.143 to 0.394 L/g VS
Alves et al. (2022) [69]Crude glycerol, primary sewage sludge, and food wasteThe inoculum was obtained from primary sewage sludge20 days37 °C7.48–7.13Biogas yields of 432.4 and 692.6 mL/g VS for 1% and 3% crude glycerol, respectively. The methane yields corresponded to 343.3 and 525.7 mL CH4/g VS for 1% and 3% v/v crude glycerol, respectively.
Table 3. Production of hydrogen using glycerol as the raw material.
Table 3. Production of hydrogen using glycerol as the raw material.
AuthorsFeedstockMicroorganismResults
Maru et al. (2016) [78]Pure and crude glycerolEscherichia coli CECT432, Escherichia coli CECT434, and Enterobacter cloacae MCM2/1Co-culture of Escherichia coli CECT 432 and Enterobacter cloacae yielded 1.26 mol H2/mol residual glycerol
Sittijunda e Reungsang (2020) [81]Pure and crude glycerolEnterobacter sp., Klebsiella sp., and Klebsiella pneumoniaeThe yields of hydrogen were 2.90 mol H2/mol pure glycerol and 2.05 mol H2/mol residual glycerol
Prakash et al. (2018) [82]Domestic wastewater and waste glycerolBacillus thuringiensis EGU4, Bacillus amyloliquefaciens strain CD16The hydrogen yield with Bacillus thuringiensis EGU4 was 100 L H2/L of residual glycerol and with Bacillus amyloliquefaciens strain CD16 was 120 L H2/L
Chen et al. (2021) [83]GycerolClostridium sp.The yields of hydrogen were 0.52 mol H2/mol glycerol for immobilized microorganisms and 0.29 mol H2/mol glycerol for suspended microorganisms
Silva et al. (2020) [84]GycerolEnterobacter and ClostridiumThe hydrogen yields were 0.25 mol H2/mol glycerol for Enterobacter and 0.01 mol H2/mol glycerol for Clostridium
Mirzoyan et al. (2019) [85]Lactose and glycerolEscherichia coliHigh H2 yield was achieved during fermentation with 1 g/L lactose at pH 7.5, with a H2 production rate of 21.94 mL/L
Toledo-Alarcon et al. (2020) [86]GlycerolClostridium sp.The presented results allowed a better understanding of the production of H2 in continuous systems and provided informationfor future industrial applications
Table 4. Ethanol production using glycerol as the raw material.
Table 4. Ethanol production using glycerol as the raw material.
AuthorsFeedstockMicroorganismResults
Sunarno et al. (2019) [97]Crude glycerolEnterobacter aerogenesWith 20 g/L of crude glycerol and the pH maintained at 7, the ethanol production was 12.33 g/L
Oh et al. (2011) [98]Crude glycerolKlebsiella pneumoniae GEM167The maximum production level was 21.5 g/L, with a productivity of 0.93 g/L/h
Stepanov e Efremenko (2017) [99]GlycerolPachysolen tannophilusThe conversion of glycerol into ethanol using immobilized yeast resulted in a yield of 90% in relation to the theoretical limit
Sunarno et al. (2020) [100]Crude glycerolEnterobacter aerogenes TISTR1468In the fermentation process without aeration, the ethanol yield was 18.78 g/L; with aeration, it was 30.31 g/L in the continuous process and 12.33 g/L in the batch process
Suzuki et al. (2015) [101]GlycerolKlebsiella variicola TB-83 e TB-83DThe strain TB-83D was effective for the production of ethanol from glycerol, and this strain was a mutant of Klebsiella variicola TB-83
Vikromvarasiri et al. (2016) [102]Crude glycerol and waste waterEnterobacter and KlebsiellaThe highest concentration of ethanol was 11.1 g/L obtained after 72 h of fermentation at an initial concentration of 45 g/L of glycerol
Lee et al. (2017) [103]Pure glycerol and crude glycerolEnterobacter aerogenes ATCC 29007 immobilizedUnder optimal conditions, the ethanol production and yield were approximately 5.38 g/L and 0.96 mol ethanol/mol glycerol with pure glycerol, respectively, while the ethanol production and yield were approximately 5.29 g/L and 0.91 mol ethanol/mol glycerol with crude glycerol, respectively
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Almeida, E.L.; Olivo, J.E.; Andrade, C.M.G. Production of Biofuels from Glycerol from the Biodiesel Production Process—A Brief Review. Fermentation 2023, 9, 869. https://doi.org/10.3390/fermentation9100869

AMA Style

Almeida EL, Olivo JE, Andrade CMG. Production of Biofuels from Glycerol from the Biodiesel Production Process—A Brief Review. Fermentation. 2023; 9(10):869. https://doi.org/10.3390/fermentation9100869

Chicago/Turabian Style

Almeida, Eugênia Leandro, José Eduardo Olivo, and Cid Marcos Gonçalves Andrade. 2023. "Production of Biofuels from Glycerol from the Biodiesel Production Process—A Brief Review" Fermentation 9, no. 10: 869. https://doi.org/10.3390/fermentation9100869

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