Next Article in Journal
Collaborative Green Innovation of Livestock Product Three-Level Supply Chain Traceability System: A Value Co-Creation Perspective
Previous Article in Journal
Sustainable Medical Waste Management Using an Intuitionistic Fuzzy-Based Decision Support System
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Bio-Nanoparticles Mediated Transesterification of Algal Biomass for Biodiesel Production

by
Madan L. Verma
1,*,
B. S. Dhanya
2,
Bo Wang
3,
Meenu Thakur
4,
Varsha Rani
5 and
Rekha Kushwaha
6
1
Department of Biotechnology, School of Basic Sciences, Indian Institute of Information Technology Una, Una 177209, Himachal Pradesh, India
2
Department of Biotechnology, Udaya School of Engineering, Udaya Nagar, Kanyakumari 629204, Tamil Nadu, India
3
Faculty of Nutrition and Food Science, School of Behavioural and Health Sciences, Australian Catholic University, Sydney, NSW 2060, Australia
4
Department of Biotechnology, Shoolini Institute of Life Sciences and Business Management, Solan 173212, Himachal Pradesh, India
5
Department of Biotechnology, Shoolini University, Solan 173229, Himachal Pradesh, India
6
Division of Biological Sciences, University of Missouri, Columbia, MO 65211, USA
*
Author to whom correspondence should be addressed.
Sustainability 2024, 16(1), 295; https://doi.org/10.3390/su16010295
Submission received: 21 November 2023 / Revised: 20 December 2023 / Accepted: 27 December 2023 / Published: 28 December 2023

Abstract

:
Immense use of fossil fuels leads to various environmental issues, including greenhouse gas emissions, reduced oil reserves, increased energy costs, global climate changes, etc. These challenges can be tackled by using alternative renewable fuels such as biodiesel. Many studies reported that biodiesel production from microalgae biomass is an environment-friendly and energy-efficient approach, with significantly improved fuel quality in terms of density, calorific value and viscosity. Biodiesel is produced using the transesterification process and the most sustainable method is utilizing enzymes for transesterification. Lipase is an enzyme with excellent catalytic activity, specificity, enantio-selectivity, compatibility and stability and hence it is applied in microalgae biodiesel production. But, difficulty in enzymatic recovery, high enzyme cost and minimal reaction rate are some of its drawbacks that have to be addressed. In this aspect, the nanotechnological approach of lipase immobilization in producing microalgae biodiesel is a promising way to increase production yield and it is due to the adsorption efficiency, economic benefit, recyclability, crystallinity, durability, stability, environmental friendliness and catalytic performance of the bio-nanoparticles used. Through increasing post-harvest biomass yield, absorption of CO2 and photosynthesis in the photobioreactor, the use of nanoparticle immobilized lipase during the generation of biodiesel from microalgae has the potential to also remove feedstock availability constraints. This review article discusses the production of microalgae biodiesel, and effect of nanoparticles and immobilized lipase nanoparticles on biodiesel production. The advantages of using lipase nanoparticles and the challenges in introducing the immobilized lipase on nanoparticles in large-scale microalgae biodiesel production are also discussed. Reducing the water and land use, energy and nutrient footprints of integrated algae-based operations must be the main goal of larger-scale experiments as well as ongoing research and development in order to expedite the adoption of microalgae-based biodiesel production. Also, the cost-effectiveness and large-scale availability of nanoparticles and the impact of lipase nanoparticles on engine performance should be analyzed for commercialization of microalgae biodiesel.

1. Introduction

Biodiesel generated from microalgae is a potential source of energy [1] and it shows an increased cetane count, a flash point, high lubricant, combustion efficiency, reduced exhaust generation, biodegradability, nitrogen oxides, positive energy balance, prevention of a sulfur shortage, renewable energy infrastructure and domestic origin [2,3]. Using microalgae for biodiesel production is advantageous due to its ease of culturing in waste-piled areas, rivers, ponds, seas, humid wastelands and municipal and industrial waste drainage [4]. Its growth does not overlap or interrupt the animal and human food chains to cause potential food sustainability or safety issues [5,6]. It has the capability of fixing and sequestering carbon content derived from carbon dioxide present in air and exhausted emission [7,8]. Moreover, many species of microalgae have significant oil content; under ideal conditions, some species can have oil content as high as 75% of their dry mass. One of the potential algae genera with significant lipid content is the Scenedesmus genus. It also possesses a significant capacity to remove nutrients during wastewater treatment and a resistance to contamination. These qualities make it a desirable input for the production of biodiesel [1].
The most popular and affordable method for producing biodiesel using an alkali, an acid, or an enzyme as a catalyst is transesterification, where the triglycerides and primary alcohol are combined in the presence of a catalyst [9]. Because of high activity under reaction conditions, catalysts like KOH/NaOH are widely utilized for producing biodiesel. However, separating a catalyst can be challenging, and a significant quantity of wastewater is produced [10]. Using enzymes is one of the sustainable techniques and it is due to their biocompatibility, specificity, biodegradability and environmental acceptability. The enzymatic transesterification process is more advantageous with a lower energy requirement and minimal environmental adverse effects [11].
One of the enzymes, lipase, shows enhanced stability, specificity, enantio-selectivity, catalytic effect and region selectivity and hence it is more suitable for the enzymatic transesterification process in biodiesel production [12]. Additional benefits of using lipase include decreased consumption of energy during the reaction due to mild reaction conditions and low temperatures, absence of soap development in the process, minimal or no side reactions, reduced sensitivity to moisture and fatty acid (FA), ease of recovering the fuel produced, compatibility with the environment and reduced alcohol consumption during the esterification reaction [11].
Even while the enzymatic transesterification process and lipase provide numerous advantages for the production of biodiesel, the disadvantages should also be taken into consideration. It should be noted that carrying out enzymatic transesterification is challenging, mostly because of issues in recovery of the enzyme, sustained instability of its functioning, cost and alcohol-induced inactivation of the enzyme. Furthermore, lipases may exhibit improper enzymatic activity. Additionally, the structure and activity of lipase are altered in the aqueous phase. Also, the interfacial area, which is governed by the substrate’s moisture content, is what determines lipase’s catalytic activity [13]. Enzyme immobilization is developed as a solution to the drawbacks of enzymatic transesterification. It also aimed to increase reaction control, prevent contamination of the product by the enzyme, enhance catalytic stability and allow for the use of different reactor topologies. It can also be used to modify enzyme activity, selectivity and specificity, reduce enzyme inhibitions or couple with purification of enzymes [14]. Also, in comparison with the chemical catalysts, lipase-immobilized nanoparticles are versatile and economical in terms of cost-effectiveness and reusable nature [15].
The IEA World Energy Outlook 2020 reported that biodiesel production volume in 2018 reached 154 billion liters and is predicted to increase by 25% in 2024 [16]. A bar chart representing the production of biodiesel from 2019 to 2025 is shown in Figure 1 [17]. However, despite the increased biofuel production volume, they are still not enough to meet the global energy need, and also developing sustainable low-energy biofuel production technology is a need globally [8,18]. Hence, researchers have utilized nanotechnology to produce microalgae biodiesel using the enzymatic transesterification process with improved yield and quality at a reduced cost.
The nano-immobilized lipase enzyme as a novel biocatalyst is a promising alternative [19]. To date, various studies have reported the increased yield of microalgae biodiesel via nanotechnology. This technology involves the immobilization of the lipase enzyme in the nanoparticles with dimensions of 1–100 nm. The bio-nanoparticles are then used in the fermentation media to promote microalgae growth to maximize the oil accumulation to produce biofuels [1]. The essential features of nanoparticles include their huge surface area relative to their volume, strong adsorption capacity and surface activity, which make them potential candidates to be essential players in the immobilization of lipase enzymes [20] for biodiesel production. This review article presents and overviews the transesterification of microalgae biomass using lipase as an enzyme source and nanoparticles as an immobilization agent for biodiesel production. It also aims to provide insights to future researchers about the challenges in microalgae biodiesel production with the incorporation of nanotechnology, thereby enhancing the large-scale biodiesel production and its commercialization.

2. Microalgae Biodiesel Production

The production of biodiesel from microalgae biomass involves several processes: microalgae strain selection, microalgae cultivation, harvesting, oil extraction and transesterification [21]. Microalgae strains may be marine- or fresh-water-based and marine strains are preferred more due to their wide occurrence. Microalgae such as Chlorella vulgaris [22], Chlorella emersonii [23], Chlorella sorokiniana [24], Schizochytrium acidic limacinum [25], C. protothecoides [26], Chlorella vulgaris ESP-31 [24], Spirulina, Thalassiosira, Nannochloropsis, Cyclotella, Scenedesmus [27], etc., are employed for generating biodiesel and they are noted in Table 1. A few characteristics determine the selection of microalgae strains: greater capacity for producing lipids; resilience to stress in photobioreactors and open raceway ponds; competent with the wild type of strains in the event that an open pond system is employed; increased absorption of carbon dioxide; robustness; ability to tolerate limited nutrient supply; tolerance to seasonal variations in temperature; capacity to generate co-products; increased productivity; increased photosynthetic effect; and the distinctive self-flocculation feature. Among the investigated strains, Schizochytrium sp., Nannochloropsis sp. and Spirulina sp. are commonly used to generate biomass to produce biofuels, with Chlorella vulgaris as the most suitable strain and it is due to the presence of high lipid content [28].
Microalgae can be cultivated in open systems such as ponds, tanks and raceway ponds, closed systems and hybrid systems that utilize characteristics of both systems. All these systems have their advantages and disadvantages that can be compared based on various parameters. Open ponds have minimal capital and operating costs with low or minimum energy requirements for culture mixing. Open systems have various disadvantages, such as high contamination risk, difficulty in scaling up, more susceptibility to adverse weather conditions, lack of agitation in these systems and low biomass production yield, whereas closed cultivation systems such as photobioreactors are more efficient in terms of quality due to highly controlled conditions during operation [38]. However, bio-fouling and overheating along with high build-up of dissolved oxygen result in growth limitation [39]. In order to overcome the challenges faced in a photobioreactor, a hybrid cultivation method is developed. This method involves two cultivation stages, aiming to combine the advantages of open ponds and photobioreactor systems [40]. In a study, the hybrid cultivation system is developed by combining a baffled reactor with a photobioreactor to cultivate Chlorella vulgaris, Scenedesmus simris and Chlorella sorokiniana in the wastewater system and it produced a biomass with lipid content varying from 44.1 to 87.9% [41].
In one of the comparative studies using marine microalga Tetraselmis sp. M8, cultivation is carried out in a photobioreactor, open raceway pond and two-stage hybrid system. The two-stage hybrid system has resulted in exponential biomass in the first tank and separate synchronized lipid stimulation in nutrient-limiting conditions. The comparative account is carried out based on growth, harvesting cycles and maximum lipid accumulation. Three harvesting cycles with 2 × 10−6 cells/mL on the 28th and 29th day are possible in the photobioreactor and open raceway pond whereas six harvesting cycles with 3 × 10−6 cells/mL are achieved with two-stage hybrid systems. The growth rate (µ) is the maximum in the case of the hybrid system (0.17) as compared to the raceway pond (0.10) and photobioreactor (0.11). Thus, maximum biomass productivity and lipid accumulation have been achieved in a hybrid system (14 g/m−2/D−1) and maximum lipid accumulation [32].
Product value, density and size are among the parameters taken into account when choosing the harvesting technique. The harvesting procedure accounts for 20–30% of the total production costs [42]. The physical harvesting method includes gravity sedimentation, centrifugation, membrane filtration and flotation approaches. However, it also has disadvantages such as a higher energy consumption and higher cost of facility implantation [43]. For the flotation process to work, algae cells must be trapped. Although centrifugal sedimentation is a quick method for harvesting algal biomass, it has the drawback of requiring maintenance [44]. Microalgae such as Spirulina and Coelastrum are ideal for filtration [45]. In the harvesting process, liquids are pumped out, homogenized and dewatered as well. Harvested biomass must be dried or dehydrated since it perishes quickly. Algal biomass can be dried using a variety of techniques, including drum drying, sun drying, fluidized bed drying, spray drying and freeze drying (lyophilization). Sun drying is the least expensive drying technique; however, it has drawbacks, such as a lengthy drying period. According to [46], freeze drying is the most costly drying process when used on a wide scale. Flocculation and coagulation are typical chemical harvesting methods. Chemicals like FeCl3, Fe2(SO4)3 or Al2(SO4)3 must be added for flocculation. The disadvantages of chemical harvesting methods are sludge formation, biomass toxicity and low lipid content [47]. Autoflocculation and bioflocculation are good examples of biological methods of harvesting microalgae [48,49]. Compared with the above chemical and physical harvesting methods, this approach is cost-efficient and environmentally viable to generate pure harvested biomass [50], but the biological approach requires a high energy input [51].
After harvesting the algal biomass, various chemical and mechanical procedures are employed to extract oil. The methods of extraction include solvent extraction, enzymatic extraction, hot oil extraction, mechanical extraction, ultrasonic aided extraction and supercritical fluid extraction [52]. Although it is useful to use enzymes in the oil extraction process to obtain fractional chemicals in the downstream phase, cost is a disadvantage. The solvent extraction approach is not nearly as effective as the supercritical fluid extraction method. The supercritical fluid extraction technique that involves liquefying CO2 under pressure yields an extract that is highly pure. The extraction of algae oil employs the stripper column approach [53]. About 60–70% of the oil can be extracted using the solvent extraction method, which uses cyclohexane, acetone, benzene, hexane and chloroform as the solvents. The solvent used to extract oil is very expensive. According to [52], the ultrasonic approach depends on the process of cavitation, which requires very little duration and extracts 76–77% of the oil. These techniques are associated with high energy consumption, significant environmental toxicity and low extraction efficiency [54].
Transesterification is an important process where the microalgae biomass’s glycerol-based ester is converted to fatty acid methyl ester. Triglycerides are an ester with a higher lipid content that produces a large amount of biodiesel. If there are any ketones, polar lipids or pigments in the algae oil, the transesterification process may be affected. In addition to using methanol as the alcohol, the transesterification process also makes use of a catalyst (KOH/NaOH). Biodiesel yielded from freshwater algal cultivation is around 400 kg kg−1 [55]. The three variables that impact the transesterification process are inhibitors, humidity and triglycerides. According to [56], a two-step transesterification procedure is advised to prevent saponification reactions. Methanol and sulfuric acid must be used in the pretreatment procedure if the amount of FFA in the algal oil is more than 2% [57]. Transesterification using enzymes is more viable and specifically immobilized enzymes increase the sustainability of biodiesel productivity [33].

3. Effect of Nanoparticles on Microalgae Biodiesel Production

A microalgae culture system is enhanced with nanomaterials that boost microalgal growth and cause lipid accumulation [58,59]. Furthermore, the use of the nanoparticle during biodiesel production from microalgae has the capacity to eliminate the restrictions associated with the availability of feedstock by improving the post-harvest biomass yield and CO2 absorption and enhancing photosynthesis in the photobioreactor [60]. The technological scheme for the production of biodiesel using bio-nanoparticles [20,45] is depicted in Figure 2 and the different types of nanoparticles used for microalgae biodiesel production [61,62,63,64] are depicted in Figure 3. In the sections that follow, the usefulness of nanotechnology in lipid accumulation, transesterification, algal culture and extraction has been evaluated.

3.1. Nanoparticles in Microalgae Cultivation and Lipid Production

The nanotechnological approach of microalgae biofuel production involves the use of different nanoparticles at different stages of biofuel production. The durability, adsorption efficiency, stability, economic advantage, environment-friendly nature, recyclability, catalytic performance, crystallinity and high storage stability are the main factors that make this method a promising approach to improve production yield and biodiesel quality [65]. For culturing algae, one of the requirements is illumination. Low levels of sunshine exposure can lead to improper development in high-density microalgae farms. Thus, employing localized surface plasmon resonance (LSPR) technology in metal nanoparticles has allowed for the resolution of the soft light lighting problem [66]. The basis of LSPR is linked oscillations of electrons (free) at a metal dielectric contact. A specific wavelength of light is specifically absorbed and scattered to cause resonant interactions between surface plasmons and photons. In an experiment with Cyanothece 51142 and Chlamydomonas reinhardtii in a photobioreactor, strong blue-colored light backscattering from a Ag nanoparticle solution is utilized to measure a 30% improvement in cell growth [67]. In another investigation, adding silver and gold nanorods to Chlorella vulgaris significantly increased the amount of carotenoids and chlorophyll. As a result, the algae’s ability to absorb light improved [68]. The primary benefit of this technique is its ability to utilize nanoparticle solutions for the development and growth of particular microalgal species. Additionally, by adjusting the size and concentration of the nanoparticles, one can prevent photoinhibition [69]. In one study, the green microalgae Chlorella vulgaris is supplemented with MgSO4 nanoparticles and an organic carbon source [50]. Both a significant decrease in the amount of glycerol used and an increase in photosynthetic efficiency are observed [70].
Microalgae produce polyunsaturated fatty acids (14–20 carbons) [71] and are able to accumulate oils up to 20–50%. This oil content can be further increased to up to 80% by manipulating growth conditions and using nanotechnology [65]. Nanoparticles are employed for photosynthetic microalgae in a medium to induce lipid buildup. The usual growing media for microalgae are reported to contain certain nutrients, but not enough for the best possible level of production. The lack of vital nutrients can be compensated by metallic nanoparticles present in some types of wastewater. Since these nanoparticles may boost microbial activity, it is feasible to put them in the medium for enhancing lipid production [72]. The functionalized groups of the hybrid nanoparticles can quicken the CO2 in the culture medium’s uptake and absorption. They supply enough CO2 for the photosynthetic system of the microalgae. It is observed that nano-Fe2O3 promoted cell growth, and via increased concentrations of the CNT, nano-Fe2O3 and nano-MgO, it enhanced lipid synthesis and total lipid content. The MgSO4 nanoparticles have the potential to promote flocculation in microalgae, which would limit their access to light and force them to produce more chlorophyll to maintain their photosynthetic activity [73]. This is probably a reaction from a defense mechanism. Green microalgae Chlorella vulgaris had grown more quickly when grown in the presence of nano-silica (size range of 38–190 nm) [74].

3.2. Nanoparticles in Harvesting of Microalgae

Microalgae biomass harvesting using the nanotechnology approach involves the use of nanoparticles to reduce the harvesting cost via decreasing energy consumption, enhancing enzyme recyclability and minimizing environmental toxicity. Nowadays, functionalized magnetic nanoparticles are applied in microalgae harvesting and it provides the separation of microalgae from the growth medium and separation of magnetic nanoparticles from microalgae [61]. Different types of nanoparticles used to harvest microalgae and their efficiency are listed in Table 2.
Due to the superiority in surface area, magnetism and biocompatibility, magnetic (Fe3O4) nanoparticles are the most widely used nanoparticles in the harvesting process. The ability of magnetic nanoparticles to readily attract and adhere to the surface of algae cells, generating a blanket that can be rapidly harvested in the presence of a magnetic force, makes them highly promising for the harvesting of microalgae. For harvesting 85% Chlorella minutissima (1 g L−1) in 60 s at pH 5 and 90% Chlorella pyrenoidosa (1 g L−1) in 60 s at pH 3, 600 and 500 mg of iron oxide nanoparticles are used, respectively [64]. It indicates the reduced time and energy required in the total cost of production, and the entire scheme of harvesting microalgae using nanoparticles is shown in Figure 4. Various agents like cationic polyacrylamide, polyethyleneimine, poly [diallyldimethylammonium chloride], [3-aminopropyl] triethoxysilane, cetrimonium bromide, polypyrrole, etc., have been applied to magnetic nanoparticles to improve harvesting efficiency [72,85].
Aside from flocculation, another difficulty that persists in the way of efficient harvesting technology is the collection of smaller algal cells, which fall into the 2–4 µm size range [86]. Magnetic flocculation has proven to be one of the most successful techniques for collecting microalgae in recent times. Harvesting magnetic nanoparticles is energy-efficient and is impacted by an external magnetic field. The microalgal biomass separates from the magnetic nanoflocculant so that it can be recycled. Magnetic iron oxide nanoparticles are being used to clear algae from fishponds and freshwater bodies. Iron oxide and 0.1 mg/mL of cationic polyacrylamide are combined to make the magnetic flocculant with the greatest flocculation capacity, which is used in the algal harvesting process. To assess the efficiency of the harvesting process, Chlorella sp. was cultured with Fe3O4 nanoparticles covered with CTAB; as a result, 96.6% of the microalgae are collected at a dose of 0.46 g particle/g cell [87].

3.3. Nanoparticles in Oil Extraction

Using nanoparticles can eliminate the costly and time-consuming solvent–lipid separation step from the conventional extraction process [88]. Nanoparticles are used to enhance the oil extraction efficiency from microalgae [54,57]. For example, cetrimonium bromide octyl triethoxysilane-coated magnetic nanoparticles, cellulose nanofibrils, carbon nanotubes and Fe2O3, MgO and ZrO2 nanoparticles have been used to extract the oils from microalgae biomass with high extraction and energy efficiency [89,90]. However, this approach is still at its early stage and its commercial hike is hindered due to an unavailability and increased cost of nanoparticles.

3.4. Nanoparticles in Transesterification Process

The specific surface area of the catalyst influences the biodiesel generation. A catalyst that has an enhanced surface/volume ratio coupled with nanoparticles works better since its surfaces contain greater active regions where reactions can take place. The transesterification is facilitated by an increased surface area of nanoparticles. The esterification process mediated by nanocatalysts has a number of special benefits, such as faster and simpler separation, longer reaction periods and a higher rate of mixing with reactants. By modifying the catalysts’ physical and chemical characteristics, the fundamental intrinsic catalytic activity and selectivity can be readily controlled [91].
Amino functionalized magnetic nanoparticles [20] are used in transesterification of microalgae biodiesel production. Nano-calcium methoxide is used for generating biodiesel from Nannochloropsis sp. It should be noted that calcium-derived catalysts continue to be the most promising since they are abundant and reasonably priced, exhibit low methanol solubility and are harmless. They are highly catalytically active and affordable, as well as environmentally beneficial. The catalyst’s significant activity was attributed to the methoxide species, which made it possible for more methanol to come into contact with the triglyceride’s carbonyl group. The substantial pore size and elevated specific surface area facilitate catalyst–substrate interaction, hence increasing transesterification efficiency. Additionally, 99.0% is the greatest conversion attained at 80 °C, and 3 percent by weight of the catalyst. This outcome suggests that nanotechnology has offered a viable and very advantageous method for producing biodiesel in an environmentally friendly manner [92].

4. Enzyme Immobilization and Nanotechnology-Driven Microalgae Biodiesel Production

The process of encapsulating enzymes in supportive materials to maintain their stabilities and reusing capacities is known as enzyme immobilization [93]. This method helps with downstream processing and offers a complete separation of the enzymes from the reaction mixture [94]. Different nanomaterials have attracted a lot of attention as vehicles for enzyme immobilization [95]. One of the many advantages that nanoparticles offer as immobilization carriers is their significantly higher surface areas when compared to conventional materials for enzyme immobilization. The activity, stability and reusability of enzymes can be increased by using nanoimmobilized enzyme systems, which could result in a significant decrease in the expenses related to their use [96]. Nanoparticles are efficient in minimizing the potential steric hindrances and protein structure distortion, while increasing the contact surface area to maximize the enzyme loading capacity and mass transfer rate [97]. In microalgae biodiesel production using enzyme immobilization in nanoparticles, the nanoparticles overcome the challenges in biodiesel production in the absence of nanoparticles and they are shown in Figure 5.
Lipases, which are the triacylglycerol acylhydrolases, function as biocatalysts that exhibit high stability and reactivity when exposed to organic solvents. They can react with a variety of substrates including esters of FAs, synthetic oils, triacylglycerides, lipids, natural oils, etc. Aspergillus, Fusarium, Mucor, Pseudomonas, Rhodotorula, Candida, Geotrichum, Penicillium and Rhizopus are among the species that are frequently listed as good producers and constitute 50% of the commercial volume of lipases [11,98,99]. Different sources of lipases used in microalgae biodiesel production are listed in Table 3. The hydrophobicity of the nanoparticle is a characteristic that helps with both the immobilization of lipase and the synthesis of biodiesel [100]. Because lipases naturally bind to hydrophobic surfaces, their immobilization on nanoparticles is distinct from that of enzymes that adsorb hydrophobically. Moreover, hydrophobic triacylglycerols and fatty acid esters have a strong attraction for hydrophobic supports. It has little affinity for glycerol, which promotes the interaction of lipases with the nanoparticles and greatly inhibits glycerol adsorption [101,102].

5. Effect of Nanoparticle-Immobilized Lipase Enzyme on Biodiesel Production

Compared with lipases in the original form, the immobilized lipases showed enhanced pH tolerance, functional stability, substrate specificity and thermal stability. This ultimately increases biofuel production yield [59,108]. To date, a wide range of nanoparticles have been investigated for this purpose, including nanosilicones, nano-metal particles, carbon nanotubes, metal–organic frameworks, magnetic nanoparticles, nanoflowers and nanofibers [109]. The nano-immobilized lipases showed the superiority of an increased surface area, enhanced stability and eased separation, compared with the lipase immobilized using conventional supporting materials [88]. Furthermore, a high reactant diffusion rate can be provided to the lipase enzyme’s active areas because of the nanomaterials’ tiny pore sizes. The factors that render nanoparticles suitable for lipase immobilization in microalgae biofuel production are shown in Figure 6.
Magnetic nanoparticles can offer a great substitute that is practical and affordable due to their enhanced thermostability and ease of recovery from reaction mixtures [110]. T. lanuginosus lipase covalently attached to aminofunctionalized magnetic nanoparticles produced 90% biodiesel conversion efficiency in one study [111]. A 100% success rate in turning oil into biodiesel using P. cepacia lipase immobilized on Fe3O4 magnetic nanoparticles is reported [112]. Lipases immobilized by magnetic nanoparticles are able to be detached from the reaction medium and are reusable, further reducing the biofuel production cost [113]. The conversion efficiency is increased by four times compared to the free lipase [114]. The magnetite-Fe3O4 and maghemite-Fe2O3 are widely employed for immobilization [115]. The magnetic support modifications are required to enhance the interaction between these nanoparticles and target lipase. In a study, amino silanes are added to the Fe3O4 nanoparticle to improve the lipase loading capacity [116]. The lipase can even be cross-linked with the incorporated amino acids in the nanoparticle using glutaraldehyde to maximize binding [117]. The silica-based nanoparticles are preferred more by the industry due to their biocompatible and non-toxic nature [118]. The silanol group can be attached on silica gel to facilitate further modifications such as the addition of functional groups such as 3–Glycidyloxypropyl trimethoxysilane to improve the immobilization efficiency [119]. In another study, lipase is immobilized on mesostructured onion-like silica via crosslinking using glutaraldehyde to produce biodiesel. This immobilization increased the reusability of the enzyme by 23 times [120]. Additionally, lipase is immobilized on silica aerogels and attained a 93% conversion rate [121]. Metal–organic-framework nanoparticles like zeolitic imidazolate framework-8 significantly improved the stability and reusability of lipase [122,123]. Carbon nanotubes are well-suited for the immobilization of lipase because of their higher mechanical properties [124]. Hybrid nanoflowers are developed to immobilize lipase for biodiesel production. The high production yield results suggested that it had economic feasibility [125]. Organic polymers are a good choice of supporting material for enzyme immobilization since the carboxyl, epoxy, hydroxyl or amino groups facilitate covalent attachment and modification. For example, the polyacrylamide-nanogel-encapsulated lipase has shown remarkable effectiveness in the synthesis of biodiesel. This allowed the lipase that has been rendered immobile to be placed at the oil–water interaction by the amphiphilic polymer shell of the nanogel. In addition, the polymer outer shell’s presence increased the lipase stability at high temperatures and methanol concentrations [126]. Different types of lipase-immobilized nanoparticles utilized in microalgae biodiesel production are tabulated in Table 4 and are discussed below:

5.1. Lipase-Fe3O4-SiO2 Hybrid Nanoparticle

Burkholderia sp. C20 [134] produced lipase and it was immobilized on Fe3O4–SiO2 that had long-chain alkyl groups acting as supports. Two methods are used to convert Chlorella vulgaris ESP-31’s microalgae oil into biodiesel. Using ultrasonic waves to break the cell walls, the M-I method recovered the microalgae oil using the solvent–chloroform and methanol. After extraction, the oil is used for transesterification. On the other hand, technique M-II employed the ESP-31 strain’s cell-wall damaged biomass directly for transesterification. Furthermore, moist microalgae biomass is used in the M-II technique for enzymatic transesterification. It is observed that the lipase could be used for up to six cycles, with at least 65% activity in the last two cycles. It is proved that biodiesel may be effectively produced through transesterification of microalgae biomass. In the M-II technique, the immobilized lipase works with an increased quantity of water and higher methanol–oil ratio and 97.25% transesterification efficiency. Thus, there is a significant chance that the suggested biocatalyst and conversion process (M-II) will be used in the industrial manufacture of microalgae biodiesel [133].

5.2. Lipase–Magnetic (Fe3O4) Nanoparticle

Magnetic nanoparticles such as Fe3O4 are promising materials to immobilize lipase to produce biofuel. The immobilized lipases can be detached from the system using a strong magnetic force to facilitate their reuse [135,136]. The lipase has been extracted from Aspergillus niger (KP001169) and it is immobilized on magnetic ferric and ferrous nanoparticles via the co-precipitation method [128,132]. These immobilized lipases are then used to produce biodiesel via the transesterification of Chlorella pyrenoidosa oils. The result suggested that the immobilization significantly increased the biodiesel production yield and the lipase retained its activity even after five production cycles. In another study, Fe3O4 superparamagnetic nanoparticles are prepared using the chemical co-precipitation method to immobilize lipase for biodiesel production via transesterification of Chlorella vulgaris oils. Similarly, the authors reported that lipase remained efficient after five production cycles [130].

5.3. Lipase–Magnetic Biosilica Nanoparticle

Numerous researchers have employed silica-based materials as a solid basis for the immobilization of enzymes [137]. Among these, diatom-derived biosilica is an inexpensive material with intriguing qualities for its use in a broad range of industrial applications [138]. Diatoms, the large unicellular algae, form unique frustrules and they are the source of the biosilicates. Diatom biosilica is a suitable raw material for its use in the biotechnological field because these biosilicates have nanoporous features with an increased surface area that is easily modifiable, an increased mechanical strength, higher stability, and better biocompatibility properties. Diatomic biosilica particles are superior to other biosilicates in several ways, including being a natural source, non-toxic and inexpensive, and having a large surface area.
The engineering of an immobilized lipase on diatomic biosilica that is magnetically recyclable is the innovative aspect of this study. It is a high-quality, stable, non-toxic particle with strong mechanical and chemical properties. Because paramagnetic nanoparticles are present in the pores of the biosilica, the magnetic biosilica does not aggregate in an aqueous solution. These characteristics enable it to be used in the transesterification procedure for the manufacture of biodiesel and make it an appropriate lipase carrier for enzymatic reactions. Large-scale applications benefit economically from the magnetic characteristic, which makes it easy to retrieve immobilized lipase from a reaction medium using a magnet. This makes biodiesel synthesis a more viable option. A hot spring water algal known as “Kamptonema formosum” is grown at three distinct temperatures, and methanol and chloroform are used to extract the algae oil. At 25 °C, the highest amount of algal biomass (1.86 g/L) is collected, and 48.7% oil is extracted. Using a thermal co-precipitation process, diatomic earth (biosilica) can be magnetized and attached with polydopamine (PDA). Schiff’s base reaction is applied for the covalent immobilization of lipase with the magnetic biosilica (MBioSi) nanoparticles. After optimizing the immobilization conditions, the immobilization medium’s initial lipase concentration was determined to be 3.0 mg/mL, which was found to be the most beneficial. The immobilization yield and the quantity of lipase on the MBioSi@PDA are determined as 67.9% and 81.9 mg/g, respectively, at this lipase concentration. This novel lipase nanoparticle is used as a biocatalyst for biodiesel generation from Kamptonema formosum with 91.2% conversion yield [127].

5.4. Lipase–Superparamagnetic Graphene Oxide (GO) Nanoparticle

Using a transesterification reaction and lipase immobilization on superparamagnetic few-layer GO, nano-biocatalysts are used to produce biodiesel. A few-layer graphene oxide (MGO) hybrid is synthesized and 3-aminopropyl triethoxysilane (MGO–AP) and a combination of glutaraldehyde and AP (MGO–AP–GA) are used to functionalize the MGO. Electrostatic interactions and covalent bonding are used to immobilize the lipase of Rhizopus oryzae (ROL) on MGO-AP, MGO and MGO-AP-GA. Kinetic characteristics, loading capability, relative action, time-course temperature stability and stability in storage are all evaluated during the nano-biocatalyst assay. The results suggested that the catalytic performance of the enzyme is significantly increased based on this immobilization. Additionally, after five cycles of the transesterification reaction, this nano-biocatalyst maintained 58.77% of its catalytic efficiency, making it the top catalyst in terms of reusability. The maximum biodiesel conversion of 71.19% is attained when ROL/MGO-AP-GA is present. The manufactured nano-biocatalyst based on functionalized and bare magnetic graphene oxide is used to convert microalgae bio-oil to biodiesel. It is compared to bare lipase immobilized on magnetic nanoparticles. The functionalization of MGO enhanced the loading capacity, thermal stability, kinetic characteristics and storage stability, according to the results. In general, the biocatalysts that are made by immobilizing enzymes through covalent bonding exhibited superior qualities [129].

5.5. Lipase–Graphene Oxide–Nickel Ferrite Nanoparticles

Candida rugosa lipase has been employed for the transesterification of algal lipids after being immobilized on graphene oxides magnetized with nickel ferrite nanoparticles. On hydrophobic supports, interfacial activation led to immobilization [93]. The ideal conditions are found to be 100 µg/mL enzyme concentrations for a 2 h incubation period, resulting in 78% immobilization efficiency. The findings showed that the immobilized enzyme is highly resistant to changes in pH and heat compared to the free enzyme; at 60 °C, it could maintain 70% of its initial activity and only 20% at pH 9. After six cycles of hydrolysis at 37 °C and pH 7, immobilized lipase maintained 47% of activity, showing its resilience and reusable property. The production efficiency of biodiesel is found to be 68% when immobilized lipase is utilized as biocatalysts [1].

6. Reuse and Recovery of Lipase Nanoparticles

The two biggest advantages of using lipase nanoparticles in the biodiesel generation are the recoverability and reusability [131,132]. The lipase nanoparticles are used in repeated cycles to generate biodiesel, and the recovery process is performed at each level. Chemical techniques are often applied for lipase nanoparticle recovery. Heterogeneous catalysts facilitate the rapid and effortless recovery of both primary and secondary products. In this mode of the catalyst, the washing step is not required. The esterification process using nanoparticles has been shown to have benefits such as rapid separation and faster reactant–catalyst mixing [135,136,137]. Easy enzyme recovery is made possible by an external magnetic field, and prior research has demonstrated that there is multiple-time recovery without significantly lowering the catalytic effect or biodiesel yield [20].

7. Challenges in Large-Scale Commercialization and the Proposed Strategies to Overcome

The challenges for commercialization include both environmental and technological barriers. Environmental barriers can be the usage of land and water, emission of greenhouse gas and loss of biodiversity [139]. Sufficient land and water are required for scaling up of microalgae biodiesel production. The effects of algal biomass production on water stress varied significantly amongst the possible sites because of regional variations in water stress. Proper planning is necessary to increase the water efficiency of large-scale algal biodiesel production. Water stress effects become quite severe when several sites are placed in highly stressed water zones, even though choosing locations according to the yield of biomass ranking could enhance economic feasibility. Water usage can be decreased by ranking sites according to Water Use Efficiency; however, the biomass production will be reduced (~25%). On the other side, the Available Water Remaining-US hotspot avoidance method could greatly lessen the effects of water stress without negatively impacting biomass yield. In contrast to the biomass yield ranking that ignores regional water stress, avoiding locations situated within elevated water stress zones could lower the water scarcity footprint for a long-term biodiesel production aim. AWARE-US might direct the geographical planning of energy system deployment and assess the effects of microalgal biofuel systems on water stress [140]. Future techno-economic assessment and life cycle assessment (LCA) studies should be carried out for envisioned commercial systems in order to confirm earlier findings based on lab- or pilot-scale experiments and to more effectively demonstrate and defend the choice of a specific production process as the best option for a given location.
Even if the use of nanoparticles in microalgae culturing, harvesting and transesterification improved efficiency, there are obstacles to overcome prior to the usage of nanoparticles in the commercial strategy. Particle size, shape, size distribution and clustering of the majority of the nanoparticles from experimental study are not well defined [141]. Thorough research on characterizing nanoparticles well is necessary prior to large-scale implementation. For maximum productivity, consideration should be given to the selection of appropriate nanoparticles, preparation techniques and time for the chosen application. Before being used, the impact of nanocatalyst implementation on engine performance, gas emission and the quality of microalgae-biofuel combustion should be thoroughly investigated and understood. Accordingly, even while nanoparticles are sufficiently available for laboratory use, their large-scale availability may provide a problem for mass use. Another barrier is the cost-effectiveness of nanocatalysts for industrial use, which could hurt business prospects because many of them are highly costly. Thus, as the economic problem is an important factor for large-scale plant installation, a complete techno-economic study is necessary to analyze whether the nanoparticles used on microalgae biodiesel are economically feasible or not. Additionally, these applications will benefit the environment in the near future by generating value-added co-products. Even if the use of nanoparticles has been shown to be environmentally beneficial, a thorough LCA is mandatory to demonstrate the benefits to the environment. Prior to commercialization, a thorough analysis of public safety, the effect on flora and fauna and the potential for biohazards is also required [20].
The impacts of microalgae are not limited to natural resources but also biodiversity. Microalgae cultivation poses a threat to biodiversity and the ecosystem. Large-scale microalgae deployment necessitates effective management and control of the cultivation process [142]. Therefore, dependence on native plant species instead of invading species that could jeopardize biodiversity for the generation of biofuel may be a wiser decision. However, large-scale microalgae farming may result in an overabundance of nutrients in the aquatic environment, endangering biodiversity [139].

8. Conclusions and Future Prospects

Driven by various environmental and economic challenges, there is an urgent demand to produce biodiesel as an alternative energy resource. Among different bioenergy microalgae feed stocks, Chlorella vulgaris shows superiority due to the high quality of microalgae-based biodiesel such as a higher calorific value, density, viscosity, etc. Even if this method is environmentally and energy-friendly, researchers are still searching for a breakthrough that will increase the yield of microalgae biofuel from the first stage to the finished product and change the entire process to a fuel that is more affordable. Nowadays, nanocatalysts are investigated to generate biodiesel from the microalgae biomass, with improved selectivity and increased production yield. In addition, the designed nanocatalysts are easily detached from the reaction system and are able to be reused to minimize the production cost. Lipase was used as an effective catalyst and it is immobilized with nanoparticles. The widely used lipase-immobilized nanoparticles are iron oxide nanoparticles, magnetic-biosilica nanoparticles, Fe3O4-SiO2 hybrid nanoparticles, superparamagnetic GO nanoparticles and GO-nickel ferrite nanoparticles.
Large-scale experiments are required to facilitate its commercial applications in the future. For large-scale microalgae biodiesel production, adequate resources of both land and water are needed, and moreover, environmentally friendly production is essential to the industry’s long-term sustainability. Careful planning is necessary to increase the water sustainability of large-scale algal biofuel production. Water stress effects are quite higher when several sites are placed in water stress zones, even though choosing sites based on biomass yield ranking would improve economic feasibility.
When several types of nanoparticles were applied at different stages of microalgae development to produce biofuel, the results were good and could lead to a revolutionary improvement in the production of large-scale microalgae biodiesel. The sustainability study of production of microalgae biofuel, however, nevertheless showed a stark requirement for additional study and innovative ideas. These ideas might help in identifying the best nanoparticles, economically speaking, for biodiesel production. Policy formulation and the application of nanoparticles will continue to be the most important factors for commercial production, particularly in poor nations, as nanoparticle application on microalgae is still a relatively new scientific topic. In order to draw in the government and non-government fuel industries, it is therefore necessary to stress management insights on appropriate policy, socioeconomic impact, advantages and constraints for the overall system. The primary obstacles to the manufacturing of biofuels are technological, financial and environmental. Cultivating algae in an enclosed setting can help to lessen environmental issues, but pretreatment processes’ resource and cost-breakeven points still need to be lowered. It is feasible to overcome these obstacles with further study and development, beginning with the generation of biofuel from microalgae and developing a commercially viable solution at a reasonable cost.

Author Contributions

Conceptualization and supervision: M.L.V. and B.W.; writing—original draft preparation: M.L.V., B.S.D., M.T., V.R. and R.K.; review and editing, artwork and schemes: B.S.D., M.T., V.R., R.K. and M.L.V. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Data are contained within the article.

Acknowledgments

Authors are grateful to the Director of Indian Institute of Information Technology Una, Himachal Pradesh, India, for providing the necessary facility to pursue the present work.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Aghabeigi, F.; Nikkhah, H.; Zilouei, H.; Bazarganipour, M. Immobilization of lipase on the graphene oxides magnetized with NiFe2O4 nanoparticles for biodiesel production from microalgae lipids. Process Biochem. 2023, 126, 171–185. [Google Scholar] [CrossRef]
  2. Mintz-Habib, N. Biofuels, Food Security, and Developing Economies; Routledge: London, UK, 2016. [Google Scholar]
  3. Liu, L.; Wu, Y.; Wang, Y.; Wu, J.; Fu, S. Exploration of environmentally friendly marine power technology-ammonia/diesel stratified injection. J. Clean. Prod. 2022, 380, 135014. [Google Scholar] [CrossRef]
  4. Collotta, M.; Champagne, P.; Mabee, W.; Tomasoni, G. Wastewater and waste CO2 for sustainable biofuels from microalgae. Algal Res. 2018, 29, 12–21. [Google Scholar] [CrossRef]
  5. Gumba, R.E.; Saallah, S.; Misson, M.; Ongkudon, C.M.; Anton, A. Green biodiesel production: A review on feedstock, catalyst, monolithic reactor, and supercritical fluid technology. Biofuel Res. J. 2016, 3, 431–447. [Google Scholar] [CrossRef]
  6. Schenk, P.M.; Thomas-Hall, S.R.; Stephens, E.; Marx, U.C.; Mussgnug, J.H.; Posten, C. Second generation biofuels: High-efficiency microalgae forbiodiesel production. Bioenergy Res. 2008, 1, 20–43. [Google Scholar] [CrossRef]
  7. Yadav, G.; Dubey, B.K.; Sen, R. A comparative life cycle assessment of microalgae production by CO2 sequestration from flue gas in outdoor raceway ponds under batch and semi-continuous regime. J. Clean. Prod. 2020, 258, 120703. [Google Scholar] [CrossRef]
  8. Liu, L.; Tang, Y.; Liu, D. Investigation of future low-carbon and zero-carbon fuels for marine engines from the view of thermal efficiency. Energy Rep. 2022, 8, 6150–6160. [Google Scholar] [CrossRef]
  9. Meher, L.C.; Sagar, D.V.; Naik, S.N. Technical aspects of biodiesel production by transesterification—A review. Renew. Sust. Energy Rev. 2006, 10, 248–268. [Google Scholar] [CrossRef]
  10. Baadhe, R.R.; Potumarthi, R.; Gupta, V.K. Lipase-Catalyzed Biodiesel Production: Technical Challenges. In Bioenergy Research: Advances and Applications; Elsevier: Amsterdam, The Netherlands, 2014; pp. 119–129. [Google Scholar] [CrossRef]
  11. Cavalcante, F.T.; Neto, F.S.; de Aguiar Falcão, I.R.; da Silva Souza, J.E.; de Moura Junior, L.S.; da Silva Sousa, P.; Rocha, T.G.; de Sousa, I.G.; de Lima Gomes, P.H.; de Souza, M.C.; et al. Opportunities for improving biodiesel production via lipase catalysis. Fuel 2021, 288, 119577. [Google Scholar] [CrossRef]
  12. Aybastıer, O.; Demir, C. Optimization of immobilization conditions of Thermomyces lanuginosus lipase on styrene–divinylbenzene copolymer using response surface methodology. J. Mol. Catal. B Enzym. 2010, 63, 170–178. [Google Scholar] [CrossRef]
  13. Borrelli, G.; Trono, D. Recombinant Lipases and Phospholipases and Their Use as Biocatalysts for Industrial Applications. Int. J. Mol. Sci. 2015, 16, 20774–20840. [Google Scholar] [CrossRef] [PubMed]
  14. Cipolatti, E.P.; Manoel, E.A.; Fernandez-Lafuente, R.; Freire, D.M.G. Support engineering: Relation between development of new supports for immobilization of lipases and their applications. Biotechnol. Res. Innov. 2017, 1, 26–34. [Google Scholar] [CrossRef]
  15. Da Fonseca, A.M.; Colares, R.P.; de Oliveira, M.M.; de Souza, M.C.; de Castro Monteiro, R.R.; dos Santos Araújo, R.; Amorim, A.V.; dos Santos, J.C.; Alcócer, J.C.; de Oliveira Pinto, O.R. Enzymatic biocatalyst using enzymes from Pineapple (Ananas comosus) peel immobilized in hydrogel beads. Rev. Eletrônica Gest. Edu Tecnol. Ambient. 2019, 23, 32. [Google Scholar] [CrossRef]
  16. Available online: https://www.iea.org/reports/world-energy-outlook-2020 (accessed on 11 November 2023).
  17. Voegele, E. IEA Expects Global Biofuels Production to Rebound in 2021. Available online: http://biodieselmagazine.com/articles/2517259/iea-expects-global-biofuelsproduction-to-rebound-in-2021 (accessed on 7 October 2023).
  18. Yang, X.; Liu, K.; Han, X.; Xu, J.; Bian, M.; Zheng, D.; Xie, H.; Zhang, Y.; Yang, X. Transformation of waste battery cathode material LiMn2O4 into efficient ultra-low temperature NH3-SCR catalyst: Proton exchange synergistic vanadium modification. J. Hazard. Mater. 2023, 459, 132209. [Google Scholar] [CrossRef] [PubMed]
  19. Chandel, H.; Kumar, P.; Chandel, A.; Verma, M.L. Biotechnological advances in biomass pretreatment for bio-renewable production through nanotechnological intervention. Biomass Convers. Biorefin. 2022, 4, 1–23. [Google Scholar] [CrossRef] [PubMed]
  20. Bin Rashid, A. Utilization of nanotechnology and nanomaterials in biodiesel production and property enhancement. J. Nanomater. 2023, 2023, 1–4. [Google Scholar] [CrossRef]
  21. Nwokoagbara, E.; Olaleye, A.K.; Wang, M. Biodiesel from microalgae: The use of multi-criteria decision analysis for strain selection. Fuel 2015, 159, 241–249. [Google Scholar] [CrossRef]
  22. Velasquez-Orta, S.; Lee, J.; Harvey, A. Alkaline in situ transesterification of Chlorella vulgaris. Fuel 2012, 94, 544–550. [Google Scholar] [CrossRef]
  23. Maceiras, R.; Rodrı, M.; Cancela, A.; Urrejola, S.; Sanchez, A. Macroalgae: Raw material for biodiesel production. Appl. Energy 2011, 88, 3318–3323. [Google Scholar] [CrossRef]
  24. Tran, D.T.; Yeh, K.L.; Chen, C.L.; Chang, J.S. Enzymatic transesterification of microalgal oil from Chlorella vulgaris ESP-31 for biodiesel synthesis using immobilized Burkholderia lipase. Bioresour. Technol. 2012, 108, 119–127. [Google Scholar] [CrossRef]
  25. Johnson, M.B.; Wen, Z. Development of an attached microalgal growth system for biofuel production. Appl. Microbiol. Biotechnol. 2010, 85, 525–534. [Google Scholar] [CrossRef] [PubMed]
  26. Xu, H.; Miao, X.; Wu, Q. High quality biodiesel production from a microalga Chlorella protothecoides by heterotrophic growth in fermenters. J. Biotechnol. 2006, 126, 499–507. [Google Scholar] [CrossRef] [PubMed]
  27. Ali, M.; Sultana, R.; Tahir, S.; Watson, I.A.; Saleem, M. Prospects of microalgal biodiesel production in Pakistan—A review. Renew. Sust. Energy Rev. 2017, 80, 1588–1596. [Google Scholar] [CrossRef]
  28. Kokkinos, K.; Karayannis, V.; Moustakas, K. Optimizing microalgal biomass feedstock selection for nanocatalytic conversion into biofuel clean energy, using fuzzy multi-criteria decision-making processes. Front. Energy Res. 2021, 8, 622210. [Google Scholar] [CrossRef]
  29. Barua, P.; Chowdhury, T.; Chowdhury, H.; Islam, R.; Hossain, N. Potential of power generation from chicken waste-based biodiesel, economic and environmental analysis: Bangladesh’s perspective. SN Appl. Sci. 2020, 2, 330. [Google Scholar] [CrossRef]
  30. Hossain, N.; Zaini, J.; Mahlia, T.M.I. Experimental investigation of energy properties for Stigonematales sp. microalgae as potential biofuel feedstock. Int. J. Sustain. Eng. 2019, 12, 123–130. [Google Scholar] [CrossRef]
  31. Khan, M.I.; Shin, J.H.; Kim, J.D. The promising future of microalgae: Current status, challenges, and optimization of a sustainable and renewable industry for biofuels, feed, and other products. Microb. Cell Fact. 2018, 17, 36. [Google Scholar] [CrossRef]
  32. Narala, R.; Garg, S.; Sharma, K.K.; Thomas-Hall, S.R.; Deme, M.; Li, Y.; Peer, M.S. Comparison of microalgae cultivation in Photobioreactor, open raceway pond, and a two-stage hybrid system. Front. Energy Res. 2016, 4, 29. [Google Scholar] [CrossRef]
  33. Yu, V.; Xu, V.; Xiao, R. Lipases from the genus Rhizopus: Characteristics, expression, protein engineering and application. Prog. Lipid Res. 2016, 64, 57–68. [Google Scholar] [CrossRef]
  34. Baldev, E.; Davoodbasha, A.; Arivalagan, P.; Nooruddin, T. Wastewater as an economical and ecofriendly green medium for microalgal biofuel production. Fuel 2021, 294, 120484. [Google Scholar] [CrossRef]
  35. Das, P.; Chandramohan, V.P.; Thangavel, M.; Arivalagan, P. A comprehensive review on the factors affecting thermochemical conversion efficiency of algal biomass to energy. Sci. Total Environ. 2020, 766, 144213. [Google Scholar] [CrossRef] [PubMed]
  36. Lal, A.; Banerjee, S.; Das, D. Aspergillus sp. assisted bioflocculation of Chlorella MJ 11/11 for the production of biofuel from the algal-fungal co-pellet. Sep. Purif. Technol. 2021, 272, 118320. [Google Scholar] [CrossRef]
  37. Derakhshandeh, M.; Atici, T.; Umran, T.U. Evaluation of wild type microalgae species biomass as carbon dioxide sink and renewable energy source. Waste Biomass Valori 2021, 12, 105–121. [Google Scholar] [CrossRef]
  38. Grima, E.; Belarbi, E.; Fernandez, F.A.; Medina, A.; Chisti, Y. Recovery of microalgal biomass and metabolites: Process options and economics. Biotechnol. Adv. 2003, 20, 491–515. [Google Scholar] [CrossRef] [PubMed]
  39. Chanquia, S.N.; Vernet, G.; Kara, S. Photobioreactors for cultivation and synthesis: Specifications, challenges, and perspectives. Eng. Life Sci. 2022, 22, 712–724. [Google Scholar] [CrossRef]
  40. Rodolfi, L.; Zittelli, G.C.; Bassi, N.; Padovani, G.; Biondi, N.; Bonini, G. Microalgae for oil: Strain selection, induction of lipid synthesis and outdoor mass cultivation in a low-cost photobioreactor. Biotechnol. Bioeng. 2008, 102, 100–112. [Google Scholar] [CrossRef] [PubMed]
  41. Khalekuzzaman, M.; Alamgir, M.; Islam, M.B.; Hasan, M. A simplistic approach of algal biofuels production from wastewater using a Hybrid Anaerobic Baffled Reactor and Photobioreactor (HABR-PBR) System. PLoS ONE 2019, 14, e0225458. [Google Scholar] [CrossRef] [PubMed]
  42. Benemann, J.R.; Oswald, W.J. Systems and economic analysis of microalgae ponds for conversion of CO2 to biomass. STIN 1994, 95, 19554. [Google Scholar]
  43. Mathimani, T.; Mallick, N. A comprehensive review on harvesting of microalgae for biodiesel–Key challenges and future directions. Renew. Sustain. Energy Rev. 2018, 91, 1103–1120. [Google Scholar] [CrossRef]
  44. Ljubic, A.; Safafar, H.; Jacobsen, C. Recovery of microalgal biomass and metabolites from homogenized, swirl flash-dried microalgae. J. Appl. Phycol. 2019, 31, 2355–2363. [Google Scholar] [CrossRef]
  45. Kumar, D.; Korstad, J.; Singh, B. Life cycle assessment of algal biofuels. In Algae and Environmental Sustainability; Springer: New Delhi, India, 2015; pp. 165–181. [Google Scholar] [CrossRef]
  46. Deborah, L.; Vidia, P.; Michael, J.; Michael, C.; Tal, M.; Charles, H.; Jefferson, W. Quantitative Uncertainty Analysis of Life Cycle Assessment for Algal Biofuel Production. Environ. Sci. Technol. 2013, 47, 687–694. [Google Scholar] [CrossRef]
  47. Ahmad, A.L.; Yasin, N.M.; Derek, C.J.C.; Lim, J.K. Comparison of harvesting methods for microalgae Chlorella sp. and its potential use as a biodiesel feedstock. Environ. Technol. 2014, 35, 2244–2253. [Google Scholar] [CrossRef] [PubMed]
  48. Şirin, S.; Trobajo, R.; Ibanez, C.; Salvadó, J. Harvesting the microalgae Phaeodactylum tricornutum with polyaluminum chloride, aluminium sulphate, chitosan and alkalinity-induced flocculation. J. Appl. Phycol. 2012, 24, 1067–1080. [Google Scholar] [CrossRef]
  49. Fuad, N.; Omar, R.; Kamarudin, S.; Harun, R.; Idris, A.; Azlina, W.W. Effective use of tannin based natural biopolymer, AFlok-BP1 to harvest marine microalgae Nannochloropsis. J. Environ. Chem. Eng. 2018, 6, 4318–4328. [Google Scholar] [CrossRef]
  50. Newkirk, G.M.; de Allende, P.; Jinkerson, R.E.; Giraldo, J.P. Nanotechnology approaches for chloroplast biotechnology advancements. Front. Plant Sci. 2021, 12, 691295. [Google Scholar] [CrossRef] [PubMed]
  51. Shurair, M.; Almomani, F.; Bhosale, R.; Khraisheh, M.; Qiblawey, H. Harvesting of intact microalgae in single and sequential conditioning steps by chemical and biological based–flocculants: Effect on harvesting efficiency, water recovery and algal cell morphology. Bioresour. Technol. 2019, 281, 250–259. [Google Scholar] [CrossRef] [PubMed]
  52. Xu, Y.; Milledge, J.J.; Abubakar, A.; Swamy, R.; Bailey, D.; Harvey, P. Effects of centrifugal stress on cell disruption and glycerol leakage from Dunaliella salina. Microalgae Biotechnol. 2015, 1, 20–27. [Google Scholar] [CrossRef]
  53. Stephenson, A.L.; Kazamia, E.; Dennis, J.S.; Howe, C.J.; Smith, S.A.; Scott, A.G. Life-cycle assessment of potential algal biodiesel production in the United Kingdom: A comparison of raceways and air-lift tubular bioreactors. Energy Fuels 2010, 24, 4062–4077. [Google Scholar] [CrossRef]
  54. Pattarkine, M.V.; Pattarkine, V.M. Nanotechnology for algal biofuels. In The Science of Algal Fuels. Cellular Origin, Life in Extreme Habitats and Astrobiology; Gordon, R., Seckbach, J., Eds.; Springer: Dordrecht, The Netherlands, 2012; Volume 25. [Google Scholar] [CrossRef]
  55. Yang, J.; Li, X.; Hu, H.; Zhang, X.; Yu, Y.; Chen, Y. Growth and lipid accumulation properties of a freshwater microalga, Chlorella ellipsoidea YJ1, in domestic secondary effluents. Appl. Energy 2011, 88, 3295–3299. [Google Scholar] [CrossRef]
  56. Chen, L.; Liu, T.; Zhang, W.; Chen, X.; Wang, J. Biodiesel production from algae oil high in free fatty acids by two-step catalytic conversion. Bioresour. Technol. 2012, 111, 208–214. [Google Scholar] [CrossRef]
  57. Zhang, Y.; Dubé, M.A.; McLean, D.D.; Kates, M. Biodiesel production from waste cooking oil: Process design and technological assessment. Bioresour. Technol. 2003, 89, 1–16. [Google Scholar] [CrossRef] [PubMed]
  58. Mota, G.F.; de Sousa, I.G.; de Oliveira, A.L.; Cavalcante, A.L.; da Silva Moreira, K.; Cavalcante, F.T.; da Silva Souza, J.E.; de Aguiar Falcão, Í.R.; Rocha, T.G.; Valério, R.B.; et al. Biodiesel production from microalgae using lipase-based catalysts: Current challenges and prospects. Algal Res. 2022, 62, 102616. [Google Scholar] [CrossRef]
  59. Chintagunta, A.D.; Ray, S.; Banerjee, R. An integrated bioprocess for bioethanol and biomanureproduction from pineapple leaf waste. J. Clean. Prod. 2017, 165, 1508–1516. [Google Scholar] [CrossRef]
  60. Kim, J.; Jia, H.; Wang, P. Challenges in biocatalysis for enzyme-based biofuel cells. Biotechnol. Adv. 2006, 24, 296–308. [Google Scholar] [CrossRef] [PubMed]
  61. Zhu, L.-D.; Hiltunen, E.; Li, Z. Using magnetic materials to harvest microalgal biomass: Evaluation of harvesting and detachment efficiency. Environ. Technol. 2019, 40, 1006–1012. [Google Scholar] [CrossRef]
  62. Li, X.; Liu, B.; Lao, Y.; Wan, P.; Mao, X.; Chen, F. Efficient magnetic harvesting of microalgae enabled by surface-initiated formation of iron nanoparticles. Chem. Eng. J. 2021, 408, 127252. [Google Scholar] [CrossRef]
  63. Almomani, F. Algal cells harvesting using cost-effective magnetic nanoparticles. Sci. Total Environ. 2020, 720, 137621. [Google Scholar] [CrossRef]
  64. Bharte, S.; Desai, K. Harvesting Chlorella species using magnetic iron oxide nanoparticles. Phycol. Res. 2019, 67, 128–133. [Google Scholar] [CrossRef]
  65. Hossain, N.; Mahlia, T.M.I.; Saidur, R. Latest development in microalgae-biofuel production with nano-additives. Biotechnol. Biofuels 2019, 12, 125. [Google Scholar] [CrossRef]
  66. Lee, Y.C.; Lee, K.; Oh, Y.K. Recent nanoparticle engineering advances in microalgal cultivation and harvesting processes of biodiesel production: A review. Bioresour. Technol. 2015, 184, 63–72. [Google Scholar] [CrossRef]
  67. Torkamani, S.; Wani, S.N.; Tang, Y.J.; Sureshkumar, R. Plasmon-enhanced microalgal growth in mini photobioreactors. Appl. Phy Lett. 2010, 97, 043703. [Google Scholar] [CrossRef]
  68. Kishi, M.; Tanaka, K.; Akizuki, S.; Toda, T. Development of a gas-permeable bag photobioreactor for energy-efficient oxygen removal from algal culture. Algal Res. 2021, 60, 102543. [Google Scholar] [CrossRef]
  69. Krishnan, S.G.; Arulraj, A.; Khalid, M.; Reddy, M.V.; Jose, R. Energy storage in metal cobaltite electrodes: Opportunities & challenges in magnesium cobalt oxide. Renew. Sustain. Energy Rev. 2021, 141, 110798. [Google Scholar] [CrossRef]
  70. Sun, Q.; Wu, Z.; Zhang, M.; Qin, Z.; Cao, S.; Zhong, F.; Li, S.; Duan, H.M.; Zhang, J. Improved gas-sensitive properties by a heterojunction of hollow porous carbon microtubes derived from sycamore fibers. ACS Sustain. Chem. Eng. 2021, 9, 14345–14352. [Google Scholar] [CrossRef]
  71. Asikainen, M.; Munter, T.; Linnekoski, J. Conversion of polar and non-polar algae oil lipids to fatty acid methyl esters with solid acid catalysts–A model compound study. Bioresour. Technol. 2015, 191, 300–305. [Google Scholar] [CrossRef] [PubMed]
  72. Nguyen, M.K.; Moon, J.Y.; Bui VK, H.; Oh, Y.K.; Lee, Y.C. Recent advanced applications of nanomaterials in microalgae biorefinery. Algal Res. 2019, 41, 101522. [Google Scholar] [CrossRef]
  73. He, M.; Yan, Y.; Pei, F.; Wu, M.; Gebreluel, T.; Zou, S.; Wang, C. Improvement on lipid production by Scenedesmus obliquus triggered by low dose exposure to nanoparticles. Sci. Rep. 2017, 7, 15526. [Google Scholar] [CrossRef]
  74. San, N.O.; Kurşungöz, C.; Tümtaş, Y.; Yaşa, Ö.; Ortac, B.; Tekinay, T. Novel one-step synthesis of silica nanoparticles from sugarbeet bagasse by laser ablation and their effects on the growth of freshwater algae culture. Particuology 2014, 17, 29–35. [Google Scholar] [CrossRef]
  75. Liu, P.; Wang, T.; Yang, Z.; Hong, Y.; Xie, X.; Hou, Y. Effects of Fe3O4 nanoparticle fabrication and surface modification on Chlorella sp. harvesting efficiency. Sci. Total Environ. 2020, 704, 135286. [Google Scholar] [CrossRef]
  76. Savvidou, M.G.; Dardavila, M.M.; Georgiopoulou, I.; Louli, V.; Stamatis, H.; Kekos, D.; Voutsas, E. Optimization of microalga Chlorella vulgaris magnetic harvesting. Nanomaterials 2021, 11, 1614. [Google Scholar] [CrossRef]
  77. Vashist, V.; Chauhan, D.; Bhattacharya, A.; Rai, M.P. Role of silica coated magnetic nanoparticle on cell flocculation, lipid extraction and linoleic acid production from Chlorella pyrenoidosa. Nat. Prod. Res. 2020, 34, 2852–2856. [Google Scholar] [CrossRef] [PubMed]
  78. Khanra, A.; Vasistha, S.; Prakash Rai, M. ZrO2 nanoparticles mediated flocculation and increased lipid extraction in chlorococcum sp. for biodiesel production: A cost effective approach. Mater. Today Proc. 2020, 28, 1847–1852. [Google Scholar] [CrossRef]
  79. Fraga-García, P.; Kubbutat, P.; Brammen, M.; Schwaminger, S.; Berensmeier, S. Bare iron oxide nanoparticles for magnetic harvesting of microalgae: From interaction behavior to process realization. Nanomaterials 2018, 8, 292. [Google Scholar] [CrossRef] [PubMed]
  80. Markeb, A.A.; Llimós-Turet, J.; Ferrer, I.; Blánquez, P.; Alonso, A.; Sánchez, A.; Moral-Vico, J.; Font, X. The use of magnetic iron oxide based nanoparticles to improve microalgae harvesting in real wastewater. Water Res. 2019, 159, 490–500. [Google Scholar] [CrossRef]
  81. Fu, Y.; Hu, F.; Li, H.; Cui, L.; Qian, G.; Zhang, D.; Xu, Y. Application and mechanisms of microalgae harvesting by magnetic nanoparticles (MNPs). Sep. Purif. Technol. 2021, 265, 118519. [Google Scholar] [CrossRef]
  82. Egesa, D.; Chuck, C.J.; Plucinski, P. Multifunctional role of magnetic nanoparticles in efficient microalgae separation and catalytic hydrothermal liquefaction. ACS Sustain. Chem. Eng. 2018, 6, 991–999. [Google Scholar] [CrossRef]
  83. Duman, F.; Sahin, U.; Atabani, A.E. Harvesting of blooming microalgae using green synthetized magnetic maghemite (γ-Fe2O3) nanoparticles for biofuel production. Fuel 2019, 256, 115935. [Google Scholar] [CrossRef]
  84. Yang, Y.; Hou, J.; Wang, P.; Wang, C.; Miao, L.; Ao, Y.; Xu, Y.; Wang, X.; Lv, B.; You, G.; et al. Interpretation of the disparity in harvesting efficiency of different types of Microcystis aeruginosa using polyethylenimine (PEI)-coated magnetic nanoparticles. Algal Res. 2018, 29, 257–265. [Google Scholar] [CrossRef]
  85. Ge, S.; Agbakpe, M.; Zhang, W.; Kuang, L. Heteroaggregation between PEI-coated magnetic nanoparticles and algae: Effect of particle size on algal harvesting efficiency. ACS Appl. Mater. Interfaces 2015, 7, 6102–6108. [Google Scholar] [CrossRef]
  86. Hu, Y.R.; Wang, F.; Wang, S.K.; Liu, C.Z.; Guo, C. Efficient harvesting of marine microalgae Nannochloropsis maritima using magnetic nanoparticles. Bioresour. Technol. 2013, 138, 387–390. [Google Scholar] [CrossRef]
  87. Wang, S.K.; Wang, F.; Hu, Y.R.; Stiles, A.R.; Guo, C.; Liu, C.Z. Magnetic flocculant for high-efficiency harvesting of microalgal cells. ACS Appl. Mater. Interfaces 2014, 6, 109–115. [Google Scholar] [CrossRef] [PubMed]
  88. Zhang, X.L.; Yan, S.; Tyagi, R.D.; Surampalli, R.Y. Biodiesel production from heterotrophic microalgae through transesterification and nanotechnology application in the production. Renew. Sustain. Energy Rev. 2013, 26, 216–223. [Google Scholar] [CrossRef]
  89. Seo, J.Y.; Praveenkumar, R.; Kim, B.; Seo, J.-C.; Park, J.-Y.; Na, J.-G.; Jeon, S.G.; Park, S.B.; Lee, K.; Oh, Y.-K. Downstream integration of microalgae harvesting and cell disruption by means of cationic surfactant-decorated Fe3O4 nanoparticles. Green. Chem. 2016, 18, 3981–3989. [Google Scholar] [CrossRef]
  90. Vasistha, S.; Khanra, A.; Clifford, M.; Rai, M.P. Current advances in microalgae harvesting and lipid extraction processes for improved biodiesel production: A review. Renew. Sustain. Energy Rev. 2021, 137, 110498. [Google Scholar] [CrossRef]
  91. Ingle, A.P.; Chandel, A.K.; Philippini, R.; Martiniano, S.E.; da Silva, S.S. Advances in nanocatalysts mediated biodiesel production: A critical appraisal. Symmetry 2020, 12, 256. [Google Scholar] [CrossRef]
  92. Teo, S.H.; Islam, A.; Taufiq-Yap, Y.H. Algae derived biodiesel using nanocatalytic transesterification process. Chem. Eng. Res. Des. 2016, 111, 362–370. [Google Scholar] [CrossRef]
  93. Verma, M.L.; Naebe, M.; Barrow, C.J.; Puri, M. Enzyme immobilisation on amino-functionalised multi-walled carbon nanotubes: Structural and biocatalytic characterisation. PLoS ONE 2013, 8, e73642. [Google Scholar] [CrossRef]
  94. Shamsudin, M.I.; Tan, L.S.; Tsuji, T. Enzyme immobilization technology in biofuel production: A review. IOP Conf. Ser. Mater. Sci. Eng. 2021, 1051, 012056. [Google Scholar] [CrossRef]
  95. Santos, S.; Puna, J.; Gomes, J. A review on bio-based catalysts (immobilized enzymes) used for biodiesel production. Energies 2020, 13, 3013. [Google Scholar] [CrossRef]
  96. Verma, M.L.; Puri, M.; Barrow, C.J. Recent trends in nanomaterials immobilized enzymes for biofuel production. Crit. Rev. Biotechnol. 2016, 36, 108–119. [Google Scholar] [CrossRef]
  97. Hwang, E.T.; Gu, M.B. Enzyme stabilization by nano/microsized hybrid materials. Eng. Life Sci. 2013, 13, 49–61. [Google Scholar] [CrossRef]
  98. Verma, M.L.; Azmi, W.; Kanwar, S.S. Microbial lipases: At the interface of aqueous and non-aqueous media. Acta Microbiol. Immunol. Hung. 2008, 55, 265–293. [Google Scholar] [CrossRef] [PubMed]
  99. Chandel, H.; Wang, B.; Verma, M.L. Microbial lipases and their applications in the food industry. In Value-Addition in Food Products and Processing Through Enzyme Technology; Elsevier: Amsterdam, The Netherlands, 2022; ISSN 978-0-323-89929-1. [Google Scholar] [CrossRef]
  100. Bartha-Vari, J.-H.; Moisa, M.E.; Bencze, L.C.; Irimie, F.-D.; Paizs, C.; Toșa, M.I. Efficient Biodiesel Production Catalyzed by Nanobioconjugate of Lipase from Pseudomonas fluorescens. Molecules 2020, 25, 651. [Google Scholar] [CrossRef] [PubMed]
  101. Zhong, L.; Feng, Y.; Wang, G.; Wang, Z.; Bilal, M.; Lv, H.; Jia, S.; Cui, J. Production and use of immobilized lipases in/on nanomaterials: A review from the waste to biodiesel production. Int. J. Biol. Macromol. 2020, 152, 207–222. [Google Scholar] [CrossRef] [PubMed]
  102. Verma, M.L. Biotechnological applications of lipases in flavour and fragrance ester production. In Microbial Technology for the Welfare of Society. Microorganisms for Sustainability; Arora, P., Ed.; Springer: Singapore, 2019; ISBN 978-981-13-8843-9. [Google Scholar] [CrossRef]
  103. Huang, J.; Xia, J.; Jiang, W.; Li, Y.; Li, J. Biodiesel production from microalgae oil catalyzed by a recombinant lipase. Bioresour. Technol. 2015, 180, 47–53. [Google Scholar] [CrossRef] [PubMed]
  104. López, B.C.; Cerdán, L.E.; Medina, A.R.; López, E.N.; Valverde, L.M.; Peña, E.H.; Moreno, P.A.G.; Grima, E.M. Production of biodiesel from vegetable oil and microalgae by fatty acid extraction and enzymatic esterification. J. Biosci. Bioeng. 2015, 119, 706–711. [Google Scholar] [CrossRef]
  105. Lee, J.H.; Lee, J.H.; Kim, D.S.; Yoo, H.Y.; Park, C.; Kim, S.W. Biodiesel production by lipases co-immobilized on the functionalized activated carbon. Bioresour. Technol. Rep. 2019, 7, 100248. [Google Scholar] [CrossRef]
  106. Guldhe, A.; Singh, B.; Rawat, I.; Permaul, K.; Bux, F. Biocatalytic conversion of lipids from microalgae Scenedesmus obliquus to biodiesel using Pseudomonas fluorescens lipase. Fuel 2015, 147, 117–124. [Google Scholar] [CrossRef]
  107. He, Y.; Wu, T.; Wang, X.; Chen, B.; Chen, F. Cost-effective biodiesel production from wet microalgal biomass by a novel two-step enzymatic process. Bioresour. Technol. 2018, 268, 583–591. [Google Scholar] [CrossRef]
  108. Singh, N.; Dhanya, B.S.; Verma, M.L. Nano-immobilized biocatalysts and their potential biotechnological applications in bioenergy sector. Mater. Sci. Energy Technol. 2020, 3, 808–824. [Google Scholar] [CrossRef]
  109. Verma, M.L.; Rao, N.M.; Barrow, C.J.; Puri, M. Suitability of recombinant lipase immobilised on functionalised magnetic nanoparticles for fish oil hydrolysis. Catalysts 2019, 9, 420. [Google Scholar] [CrossRef]
  110. Ngo, T.P.; Li, A.; Tiew, K.W.; Li, Z. Efficient transformation of grease to biodiesel using highly active and easily recyclable magnetic nanobiocatalyst aggregates. Bioresour. Technol. 2013, 145, 233–239. [Google Scholar] [CrossRef] [PubMed]
  111. Sakai, S.; Liu, Y.; Yamaguchi, T.; Watanabe, R.; Kawabe, M.; Kawakami, K. Production of butyl-biodiesel using lipase physically-adsorbed onto electrospun polyacrylonitrile fibers. Bioresour. Technol. 2010, 101, 7344–7349. [Google Scholar] [CrossRef]
  112. Huang, J.; Wang, J.; Huang, Z.; Liu, T.; Li, H. Photothermal technique-enabled ambient production of microalgae biodiesel: Mechanism and life cycle assessment. Bioresour. Technol. 2023, 369, 128390. [Google Scholar] [CrossRef] [PubMed]
  113. Amini, Z.; Ilham, Z.; Ong, H.C.; Mazaheri, H.; Chen, W.H. State of the art and prospective of Lipase- catalyzed transesterification reaction for biodiesel production. Energy Convers. Manag. 2017, 141, 339–353. [Google Scholar] [CrossRef]
  114. Netto, C.G.; Toma, H.E.; Andrade, L.H. Superparamagnetic nanoparticles as versatile carriersand supporting materials for enzymes. J. Mol. Catal. B Enzym. 2013, 85, 71–92. [Google Scholar] [CrossRef]
  115. Xie, W.; Zang, X. Covalent immobilization of Lipase onto aminopropyl-functionalizedhydroxyapatite-encapsulated-γ-Fe2O3 nanoparticles: A magnetic biocatalyst for interesterification of soybean oil. Food Chem. 2017, 227, 397–403. [Google Scholar] [CrossRef]
  116. Knothe, G. Analyzing biodiesel: Standards and other methods. J. Am. Oil Chem. Soc. 2006, 83, 823–833. [Google Scholar] [CrossRef]
  117. Shaw, S.Y.; Chen, Y.J.; Ou, J.J.; Ho, L. Preparation and characterization of Pseudomonas putida esterase immobilized on magnetic nanoparticles. Enzym. Microb. Technol. 2006, 39, 1089–1095. [Google Scholar] [CrossRef]
  118. Tang, L.; Cheng, J. Nonporous silica nanoparticles for nanomedicine application. Nano Today 2013, 8, 290–312. [Google Scholar] [CrossRef]
  119. Babaki, M.; Yousefi, M.; Habibi, Z.; Mohammadi, M.; Yousefi, P.; Mohammadi, J.; Brask, J. Enzymatic production of biodiesel using lipases immobilized on silica nanoparticles as highly reusable biocatalysts: Effect of water, t-butanol and blue silica gel contents. Renew. Energy 2016, 91, 196–206. [Google Scholar] [CrossRef]
  120. Jun, S.H.; Lee, J.; Kim, B.C.; Lee, J.E.; Joo, J.; Park, H.; Lee, J.H.; Lee, S.M.; Lee, D.; Kim, S. Highly efficient enzyme immobilization and stabilization within meso-structured onion-like silica for biodiesel production. Chem. Mater. 2012, 24, 924–929. [Google Scholar] [CrossRef]
  121. Arumugam, A.; Thulasidharan, D.; Jegadeesan, G.B. Process optimization of biodiesel production from Hevea brasiliensis oil using lipase immobilized on spherical silica aerogel. Renew. Energy 2018, 116, 755–761. [Google Scholar] [CrossRef]
  122. Bilal, M.; Adeel, M.; Rasheed, T.; Iqbal, H.M. Multifunctional metal–organic frameworks-based biocatalytic platforms: Recent developments and future prospects. J. Mater. Res. Technol. 2019, 8, 2359–2371. [Google Scholar] [CrossRef]
  123. Lyu, F.; Zhang, Y.; Zare, R.N.; Ge, J.; Liu, Z. One-pot synthesis of protein-embedded metal–organic frameworks with enhanced biological activities. Nano Lett. 2014, 14, 5761–5765. [Google Scholar] [CrossRef]
  124. Goyanes, S.; Rubiolo, G.; Salazar, A.; Jimeno, A.; Corcuera, M.; Mondragon, I. Carboxylation treatment of multiwalled carbon nanotubes monitored by infrared and ultraviolet spectroscopies and scanning probe microscopy. Diam. Relat. Mater. 2007, 16, 412–417. [Google Scholar] [CrossRef]
  125. Jiang, W.; Wang, X.; Yang, J.; Han, H.; Li, Q.; Tang, J. Lipase-inorganic hybrid nanoflower constructed through biomimetic mineralization: A new support for biodiesel synthesis. J. Colloid. Interface Sci. 2018, 514, 102–107. [Google Scholar] [CrossRef]
  126. Verma, M.L.; Barrow, C.J.; Puri, M. Nanobiotechnology as a novel paradigm for enzyme immobilization and stabilisation with potential applications in biofuel production. Appl. Microbiol. Biotechnol. 2013, 97, 23–39. [Google Scholar] [CrossRef]
  127. Acıkgoz-Erkaya, I.; Bayramoglu, G.; Akbulut, A.; Arica, M.Y. Immobilization of Candida rugosa lipase on magnetic biosilica particles: Hydrolysis and transesterification studies. Biotechnol. Bioproc E 2021, 26, 827–840. [Google Scholar] [CrossRef]
  128. Shalini, P.; Deepanraj, B.; Vijayalakshmi, S.; Ranjitha, J. Synthesis and characterization of Lipase immobilized magnetic nanoparticles and its role as a catalyst in biodiesel production. Mater. Today Proc. 2021, 80, 2725–2730. [Google Scholar] [CrossRef]
  129. Nematian, T.; Shakeri, A.; Salehi, Z. Lipase immobilized on functionalized superparamagnetic few-layer graphene oxide as an efficient nanobiocatalyst for biodiesel production from Chlorella vulgaris bio-oil. Biotechnol. Biofuels 2020, 13, 57. [Google Scholar] [CrossRef] [PubMed]
  130. Nematian, T.; Salehi, Z.; Shakeri, A. Conversion of bio-oil extracted from Chlorella vulgaris micro algae to biodiesel via modified superparamagnetic nano-biocatalyst. Renew. Energy 2020, 146, 1796–1804. Available online: https://ideas.repec.org/a/eee/renene/v146y2020icp1796-1804.html (accessed on 11 November 2023). [CrossRef]
  131. Pico, E.A.; Lopez, C.; Cruz-Izquierdo, Á.; Munarriz, M.; Iruretagoyena, F.J.; Serra, J.L.; Llama, M.J. Easy reuse of magnetic crosslinked enzyme aggregates of lipase B from Candida antarctica to obtain biodiesel from Chlorella vulgaris lipids. J. Biosci. Bioeng. 2018, 126, 451–457. [Google Scholar] [CrossRef] [PubMed]
  132. Duraiarasan, S.; Razack, S.A.; Manickam, A.; Munusamy, A.; Syed, M.B.; Ali, M.Y.; Ahmed, G.M.; Mohiuddin, M.S. Direct conversion of lipids from marine microalga C. salina to biodiesel with immobilized enzymes using magnetic nanoparticle. J. Environ. Chem. E 2016, 4, 1393–1398. [Google Scholar] [CrossRef]
  133. Fattah, I.M.R.; Noraini, M.Y.; Mofijur, M.; Silitonga, A.S.; Badruddin, I.A.; Khan, T.M.Y.; Ong, H.C.; Mahlia, T.M.I. Lipid Extraction Maximization and Enzymatic Synthesis of Biodiesel from Microalgae. Appl. Sci. 2020, 10, 6103. [Google Scholar] [CrossRef]
  134. Mehde, A.A.; Mehdi, W.A.; Severgun, O.; Cakar, S.; Ozacar, M. Lipase-based on starch material as a development matrix with magnetite crosslinked enzyme aggregates and its application. Int. J. Biol. Macromol. 2018, 120, 1533–1543. [Google Scholar] [CrossRef] [PubMed]
  135. He, S.; Feng, Y.; Ren, H.; Zhang, Y.; Gu, N.; Lin, X. The impact of iron oxide magnetic nanoparticles on the soil bacterial community. J. Soils Sediments 2011, 11, 1408–1417. [Google Scholar] [CrossRef]
  136. Toh, P.Y.; Yeap, S.P.; Kong, L.P.; Ng, B.W.; Chan, D.J.C.; Ahmad, A.L.; Lim, J. Magnetophoretic removal of microalgae from fishpond water: Feasibility of high gradient and low gradient magnetic separation. Chem. Eng. J. 2012, 211–212, 22–30. [Google Scholar] [CrossRef]
  137. Yan, X.H.; Xue, P. Tailoring magnetic mesoporous silica spheres-immobilized lipase for kinetic resolution of methyl 2-bromopropionate in a co-solvent system. Res. Chem. Intermed. 2018, 44, 4295–4306. [Google Scholar] [CrossRef]
  138. Bayramoglu, G.; Akbulut, A.; Ozalp, V.C.; Arica, M.Y. Immobilized lipase on micro-porous biosilica for enzymatic transesterification of algal oil. Chem. Eng. Res. Des. 2015, 95, 12–21. [Google Scholar] [CrossRef]
  139. Olabi, A.G.; Alami, A.H.; Alasad, S.; Aljaghoub, H.; Sayed, E.T.; Shehata, N.; Rezk, H.; Abdelkareem, M.A. Emerging technologies for enhancing microalgae biofuel production: Recent progress, barriers, and limitations. Fermentation 2022, 8, 649. [Google Scholar] [CrossRef]
  140. Xu, H.; Lee, U.; Coleman, A.M.; Wigmosta, M.S.; Wang, M. Assessment of algal biofuel resource potential in the United States with consideration of regional water stress. Algal Res. 2019, 37, 30–39. [Google Scholar] [CrossRef]
  141. Mirzajanzadeh, M.; Tabatabaei, M.; Ardjmand, M.; Rashidi, A.; Ghobadian, B.; Barkhi, M.; Pazouki, M. A novel soluble nano-catalysts in diesel–biodiesel fuel blends to improve diesel engines performance and reduce exhaust emissions. Fuel 2015, 139, 374–382. [Google Scholar] [CrossRef]
  142. Kamilli, K.; Ofner, J.; Zetzsch, C.; Held, A. Formation of halogen-induced secondary organic aerosol (XOA). In Proceedings of the EGU General Assembly 2013 (EGU2013-11969), Vienna, Austria, 7–12 April 2013; Available online: https://ui.adsabs.harvard.edu/abs/2013EGUGA..1511969K/abstract (accessed on 11 November 2023).
Figure 1. Production of biodiesel from the year 2019 to 2025, as reported by the international energy agency.
Figure 1. Production of biodiesel from the year 2019 to 2025, as reported by the international energy agency.
Sustainability 16 00295 g001
Figure 2. Technological scheme for the production of biodiesel using bio-nanoparticles.
Figure 2. Technological scheme for the production of biodiesel using bio-nanoparticles.
Sustainability 16 00295 g002
Figure 3. Different types of nanoparticles used for microalgae biodiesel production.
Figure 3. Different types of nanoparticles used for microalgae biodiesel production.
Sustainability 16 00295 g003
Figure 4. Effect of magnetic iron oxide nanoparticles on harvesting microalgae.
Figure 4. Effect of magnetic iron oxide nanoparticles on harvesting microalgae.
Sustainability 16 00295 g004
Figure 5. Importance of nanotechnology-driven enzyme-immobilized microalgae biodiesel.
Figure 5. Importance of nanotechnology-driven enzyme-immobilized microalgae biodiesel.
Sustainability 16 00295 g005
Figure 6. Factors rendering nanoparticles ideal for enzyme immobilization in microalgae biodiesel production.
Figure 6. Factors rendering nanoparticles ideal for enzyme immobilization in microalgae biodiesel production.
Sustainability 16 00295 g006
Table 1. Microalgae cells as renewable feedstock for production of biodiesel.
Table 1. Microalgae cells as renewable feedstock for production of biodiesel.
Sr. No.Name of MicroalgaeRemarksReferences
1.Spirulina platensisGood diesel index, high density[29]
2.Chlorella protothecoidesHigh cetane number[30]
3.Chlorella sp.High viscosity[30]
4.Botryococcus braunii80% lipid accumulation[31]
7.Tetraselmis sp. M8Lipase catalyzed transesterification[32]
8.Croto megalocarpusImmobilized lipase for better production[33]
9.Chlorella sorokiniana44.1–87.9% lipid accumulation[33]
10.Scenedesmus sp.Lipid accumulation in 20 days[34]
12.Chlorella sorokinianaLipid accumulation[35]
13.Chlorella vulgaris95% yield[35]
16.Chlorella sp. MJ 11/11Improved quality of bio-oil[36]
17.Scenedesmus quadricaudaHigh amount of oleic acid[37]
Table 2. Nanotechnology-mediated microalgae harvesting.
Table 2. Nanotechnology-mediated microalgae harvesting.
S. No.MicroalgaeNanoparticle UsedHarvesting Efficiency References
1.Chlorella zofingiensisIron nanoparticles98%[62]
2.Chlorella vulgarisMagnetic nanoparticles (MNPs; Fe-MNP-I and Fe-MNP-II)95%[63]
3.Chlorella sp.Fe3O4 nanoparticle95%[75]
4.Chlorella vulgarisNaked magnetite (Fe3O4)99%[76]
5.Chlorella pyrenoidosa and Chlorella minutissimaIron oxide nanoparticles90%[64]
6.Chlorella vulgarisYttrium iron oxide (Y3Fe5O12)90%[61]
7.Chlorella pyrenoidosaMagnetic (Fe3O4)–silica core–shell nanoparticlesIncreased[77]
8.Chlorococcum sp.Zirchonium di-oxide (ZrO2-Np)Increased[78]
9.Scenedesmus ovalternus and Chlorella vulgarisBare iron oxide95%[79]
10.Scenedesmus sp.Magnetite-based nanoparticles (Fe3O4 NPs)95%[80]
11.Nannochloropsis maritimeNaked magnetic nanoparticles99.0%[81]
12.Scenedesmus obliquusZn- and Mg-doped ferrite magnetic nanoparticles99%[82]
13.Microcystis aeruginosaMagnetic maghemite (γ-Fe2O3)82.4%[83]
14.Microcystis aeruginosaPolyethylenimine-coated magnetic nanoparticlesNA[84]
Table 3. Sources of lipase used in microalgae biodiesel production.
Table 3. Sources of lipase used in microalgae biodiesel production.
Sources of LipaseTime (h)Conversion (%)References
Rhizomucor miehei2490%[103]
Candida antarctica492.6%[104]
Candida rugosa493%[105]
Pseudomonas fluorescens1295%[106]
Thermomyces lanuginosus4881.64%[107]
Table 4. Lipase nanoparticles for microalgae biodiesel production.
Table 4. Lipase nanoparticles for microalgae biodiesel production.
Lipase NanoparticlesMicroalgaCatalytic CyclesReference
Lipase–Magnetic Biosilica NanoparticleKamptonema formosum-[127]
Lipase–Magnetic (Fe3O4) NanoparticleChlorella pyrenoidosa5 cycles[128]
Lipase–Superparamagnetic–Graphene Oxide NanoparticleChlorella vulgaris5 cycles[129]
Lipase-Fe3O4 Superparamagnetic NanoparticleChlorella vulgaris5 cycles[130]
Lipase-Aminated Magnetic NanoparticleChlorella vulgaris var L310 cycles[131]
Lipase–Magnetic (Fe3O4) NanoparticleChlorella salina10 cycles[132]
Lipase-Fe3O4-SiO2 Hybrid NanoparticlesChlorella vulgaris ESP-314 cycles[133]
Lipase–Graphene Oxide–Nickel Ferrite NanoparticlesScenedesmus obliquus6 cycles[1]
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

Verma, M.L.; Dhanya, B.S.; Wang, B.; Thakur, M.; Rani, V.; Kushwaha, R. Bio-Nanoparticles Mediated Transesterification of Algal Biomass for Biodiesel Production. Sustainability 2024, 16, 295. https://doi.org/10.3390/su16010295

AMA Style

Verma ML, Dhanya BS, Wang B, Thakur M, Rani V, Kushwaha R. Bio-Nanoparticles Mediated Transesterification of Algal Biomass for Biodiesel Production. Sustainability. 2024; 16(1):295. https://doi.org/10.3390/su16010295

Chicago/Turabian Style

Verma, Madan L., B. S. Dhanya, Bo Wang, Meenu Thakur, Varsha Rani, and Rekha Kushwaha. 2024. "Bio-Nanoparticles Mediated Transesterification of Algal Biomass for Biodiesel Production" Sustainability 16, no. 1: 295. https://doi.org/10.3390/su16010295

APA Style

Verma, M. L., Dhanya, B. S., Wang, B., Thakur, M., Rani, V., & Kushwaha, R. (2024). Bio-Nanoparticles Mediated Transesterification of Algal Biomass for Biodiesel Production. Sustainability, 16(1), 295. https://doi.org/10.3390/su16010295

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