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. 2025 Sep 22:ETLS20240004. doi: 10.1042/ETLS20240004

Microalgae-based biodiesel: integrating AI, CRISPR and nanotechnology for sustainable biofuel development

Fariha Kanwal 1,, Ambreen Aslam 2, Angel A J Torriero 3,
PMCID: PMC12599237  PMID: 40982615

Abstract

Microalgae are a promising feedstock for biodiesel due to their rapid growth, high lipid content and ability to use non-arable land and wastewater. This review synthesises recent advances in artificial intelligence (AI)-driven strain optimisation, engineering, nanotechnology-assisted processing, and life cycle and technoeconomic insights to evaluate pathways for industrialisation. Over the past decade (2015–2024), genetic engineering and, more recently, AI-guided strain selection have improved lipid productivity by up to 40%. Cultivation advances, including hybrid photobioreactor–open pond systems and precision pH/CO2 control, have enhanced biomass yields while reducing costs. Innovation in lipid extraction, such as supercritical CO2 and microwave-assisted methods, now achieves >90% yields with lower toxicity, while magnetic nanoparticle-assisted harvesting and electroflocculation have reduced energy inputs by 20–30%. Life cycle analyses (net energy ratio ~2.5) and integration of high-value co-products (e.g. pigments and proteins) underscore the need to align biological innovations with techno-economic feasibility. This review uniquely integrates advances in AI, CRISPR and nanotechnology with life cycle and techno-economic perspectives, providing a comprehensive framework that links laboratory-scale innovation to industrial feasibility and positions microalgal biodiesel as a viable contributor to global decarbonisation strategies.

Keywords: biodiesel, harvesting, microalgae, sustainability, transesterification

Introduction

Over the past two decades, global energy strategies have increasingly shifted toward renewable technologies to mitigate climate change, improve energy security and stabilise economies [1]. The extensive use of fossil fuels has caused severe environmental consequences, including carbon dioxide emissions, biodiversity loss and pollution [2–4].

Recent advances in renewable energy technologies – such as solar photovoltaics, wind and biofuels – have reduced renewable energy costs by 50–80% since 2010, enabling decentralised power systems that expand energy access in marginalised regions [5–8]. This transition has reshaped geopolitical influence, with nations leading in renewables gaining strategic leverage over fossil fuel-exporting economies.

Within this context, biodiesel has emerged as a prominent renewable transport fuel, contributing over 50% of global biofuel output and serving as a carbon-neutral alternative to conventional diesel [9,10]. Produced through transesterification of long-chain fatty acid methyl esters (FAMEs), biodiesel aligns with existing engine infrastructure and offers immediate decarbonisation potential.

Feedstock development has progressed through four generations (Figure 1): first-generation edible crops, second-generation non-edible crops, third-generation microalgae, and now fourth-generation genetically engineered microalgae using tools such as CRISPR-Cas9 [11]. First-generation biodiesel faced ethical challenges due to food competition, while second-generation non-edible feedstocks were constrained by high collection costs and limited caloric efficiency. Third-generation microalgae offer lipid productivities exceeding 40% of dry weight, rapid doubling times and the ability to grow on wastewater or saline resources [10]. Fourth-generation systems build upon these traits by incorporating genetic engineering and synthetic biology to enhance stress tolerance and compatibility with integrated biorefineries, creating scalable and resource-efficient pathways.

Figure 1. Evolution of biodiesel feedstocks across four generations, illustrating the transition from edible crops to genetically engineered microalgae (GEM) and the corresponding improvements in efficiency. Created by the authors.

Figure 1

This review synthesises recent technological breakthroughs – including artificial intelligence (AI)-guided strain optimisation, CRISPR-based engineering, hybrid photobioreactor (PBR)–open pond cultivation, magnetic nanoparticle-assisted harvesting, supercritical CO₂ extraction and nanocatalyst-assisted transesterification – and evaluates their implications for scalability, sustainability and integration into circular bioeconomy models. Unlike recent reviews in Fuel, Algal Research and Renewable Energy, which have emphasised mainly cultivation and conventional processing, this article integrates these advances with life cycle (net energy ratio [NER]) metrics and techno-economic feasibility, providing a forward-looking perspective that links laboratory innovation to industrial application.

Biodiesel production from microalgae offers a sustainable approach by reusing and integrating carbon resources from the environment, contributing to the global goal of reducing petroleum use and environmental pollution [9,12–15]. Microalgae, more efficient than macroalgae due to their higher lipid productivity and easier cultivation, are rich in compounds like lipids, proteins and carbohydrates. In addition to environmental benefits, economic sustainability remains critical for biofuel viability. Profitability and favourable investment conditions influence technology adoption and scale-up, as highlighted by analyses of investment decision-making in emerging industries [16,17]. These factors reinforce the importance of techno-economic feasibility, life cycle metrics (NER ~2.5), and co-product valorisation in aligning microalgal biodiesel development with industrial and investor expectations.

Microalgae as a feedstock for biodiesel production

Microalgae are photosynthetic organisms thriving in aquatic environments, including marine and freshwater habitats. These organisms, which can be unicellular or multicellular, exhibit remarkable adaptability, thriving under diverse conditions and displaying various metabolic modes such as autotrophy, heterotrophy, mixotrophy and photoheterotrophy [18,19]. Importantly, their cultivation does not compete with food production as they can grow in freshwater, saltwater, saline water and even wastewater.

Microalgae are primarily composed of lipids, carbohydrates and biomass, with their lipid content making them highly suitable for biodiesel production. Lipids, which are biological molecules dissolvable in organic solvents, are categorised into polar and non-polar lipids, with fatty acids serving as their key components. Fatty acids vary in chain length, saturation and structure, forming either neutral lipids (e.g. triacylglycerols) or polar lipids (e.g. phospholipids) [20–24]. The lipid synthesis process in microalgae occurs primarily in the chloroplast, where glucose undergoes glycolysis to generate acetyl-CoA, a precursor for lipid production, as depicted in Figure 2 [10, 11 and 21].

Figure 2. Schematic overview of lipid synthesis in microalgae: glucose undergoes glycolysis to form acetyl-CoA, which is converted into fatty acids in the chloroplast and subsequently assembled into triacylglycerols (TAGs) in the endoplasmic reticulum. These pathways underpin microalgal biodiesel production. Created by the authors.

Figure 2

Certain microalgae species, such as Chlamydomonas reinhardtii (21% lipid content), Spirulina platensis (8% lipid content) and Chlorella species (19% lipid content), have garnered significant research attention due to their potential as biodiesel feedstocks [25,26]. Oleaginous microalgae, characterised by their high oil yields, represent particularly promising candidates. Detailed lipid content and fatty acid profiles for various algal species are presented in Table 1, which underscores the variability in lipid productivity across species [25,26].

Table 1. Lipid content and fatty acid profiles of selected microalgal species.

Sr. no Mode Species Lipid content %
(dry cell weight)
FA profile Ref.
1 Autotrophic Nannochloropsis sp. 12–53 C16:0;C16:1;C18:1;C18:2;C20:4;C20:5 [27]
2 Autotrophic Dunaliella sp. 17.5–67 C16:0;C16:1;C18:0;C18:1;C18:2;C18:3 [28]
3 Autotrophic Phaeodactylum tricornutum 20–40 C16:0;C16:1;C18:0;C18:1;C18:2;C20:5 [29]
4 Heterotrophic Crypthecodinium cohnii 51 C16:0;C18:1;C18:2;C18:3;C22:6 [30]
5 Mixotrophic Dunaliella tertiolecta 17.5–67 C16:0;C18:1;C18:2;C18:3 [30]
6 Autotrophic Chlamydomonas sp. 20 C16:0;C18:0;C18:1;C18:2;C18:3 [29]
7 Autotrophic Chlorella sp. 40 C16:0;C18:0;C18:1;C18:2 [31]
8 Autotrophic Desmodesmus sp. EJ8-10. 19.4–28 C16:0;C18:1;C18:2;C18:3 [9]
9 Autotrophic Scenedesmus abundans 17.3–32.8 C16:0;C18:0;C18:1;C18:2 [32]
10 Mixotrophic Euglena gracilis 24.81 C14:0;C16:0;C18:0;C18:1;C18:2 [33]
11 Autotrophic Botryococcus braunii 35.9–62.7 C16:0;C18:1;C18:2 [34]
12 Autotrophic Nannochloropsis oceanica 49.0–53.2 C16:0;C18:1;C20:5;C22:6 [35]
13 Autotrophic Boekelovia hooglandii 59 C16:0;C18:0;C18:1;C18:2;C18:3 [36]
14 Heterotrophic Schizochytrium limacinum 40–45 C16:0;C18:1;C20:5;C22:6 [20]
15 Autotrophic Isochrysis galbana 30–35 C16:0;C18:1;C20:5;C22:6 [37]
16 Autotrophic Coelastrella sp. 44–46 C16:0;C18:0;C18:1;C18:2 [38]
17 Autotrophic Verrucodesmus verrucosus 43–44 C16:0;C18:0;C18:1;C18:2;C18:3 [38]

Efficient cultivation is critical for maximising lipid production and biomass yield. Three primary systems dominate microalgae cultivation: open raceway ponds, closed PBRs and hybrid systems. Open systems, while economical, are vulnerable to contamination, whereas PBRs offer controlled conditions for high-quality biomass. Hybrid systems leverage the strengths of both, initially cultivating microalgae in PBRs under optimal conditions, followed by nutrient-depleted open systems to enhance lipid accumulation [25,34,39]. Environmental factors significantly influence lipid synthesis, including light intensity, temperature and nutrient availability. Additionally, salinity stress and pH optimisation have been shown to further enhance lipid accumulation [18,40–42].

Harvesting and dewatering microalgae biomass involves thickening to increase solid concentration and dewatering for separation. Techniques include physical methods like flotation, filtration and centrifugation and chemical, biological, magnetic and electrochemical methods. Emerging approaches, such as magnetic harvesting using nanoparticles and electroflocculation, show the capacity to reduce energy costs and environmental impact [43–45].

Lipid extraction is a pivotal step in biodiesel production, employing hexane, chloroform and methanol solvents. Advanced techniques, including supercritical CO₂ extraction, provide high yields with minimal toxicity but remain cost-prohibitive due to the high pressures involved [46–49]. These processes, alongside ongoing innovations in cultivation and harvesting, position microalgae as a viable and sustainable feedstock for biodiesel production.

Biodiesel production processes

Microalgae oil is a promising feedstock for biodiesel due to its sustainability and high lipid content. While transesterification remains the predominant conversion route for biodiesel, alternative methods such as hydroprocessing and pyrolysis are also under investigation. However, these pathways are less mature and not yet widely applied to microalgal feedstocks [50]. Nonetheless, microalgae oil’s high viscosity and low volatility present challenges for engine performance. These issues are addressed through transesterification, a chemical process that converts triglycerides into biodiesel, specifically FAMEs, and glycerol using alcohol (typically methanol) and a catalyst [51]. The lipid extraction techniques preceding this process are illustrated in Figure 3.

Figure 3. Lipid extraction techniques from harvested algal biomass, comparing conventional methods (e.g. Folch, Bligh and Dyer and Soxhlet) with eco-friendly innovations like supercritical fluids, ionic liquids, ultrasound, microwaves and enzyme-assisted processes.

Figure 3

Transesterification methods

Two primary approaches to transesterification are non-catalytic and catalytic methods, each offering distinct advantages and challenges. Non-catalytic transesterification, or supercritical transesterification, operates under extreme temperature and pressure conditions and offers rapid reaction times, high yields and simplified purification. This method tolerates diverse feedstocks but is energy-intensive and requires a higher oil-to-alcohol molar ratio [25,34,52].

The microalgae species Chlorella vulgaris has been extensively studied for its high lipid productivity and adaptability to diverse cultivation environments. The effectiveness of in-situ transesterification under subcritical conditions was demonstrated, achieving a 74.6% FAME yield at 220°C using biomass with 80 wt% moisture content [53]. This process optimised methanol usage to 8 mL per gram of biomass and consumed 0.47 kWh of power, showcasing its energy efficiency relative to traditional methods. Integrating lipid extraction with transesterification eliminated intermediate drying steps, significantly reducing overall processing costs. Such advancements underscore the importance of process optimisation to achieve scalable and sustainable biodiesel production from Chlorella vulgaris. These findings also highlight the potential of combining extraction and conversion steps into a single streamlined process, minimising energy consumption and material waste (Figure 4) [54].

Figure 4. Conversion of lipids to biodiesel via transesterification processes, including non-catalytic methods and catalytic techniques (homogeneous, heterogeneous, biocatalytic and nanocatalytic).

Figure 4

Catalytic transesterification processes, classified into homogeneous, heterogeneous, biocatalytic and nanocatalytic methods, use catalysts to improve reaction rates and biodiesel yields [52,55]. Homogeneous catalysts include alkali catalysts like sodium hydroxide and acid catalysts like sulphuric acid. While alkali catalysts provide high conversion rates under mild conditions, acid catalysts are more effective for feedstocks with high free fatty acid content [50,56–61]. Heterogeneous catalysts are solid catalysts such as calcium oxide (CaO) and magnesium oxide (MgO) that offer reusability and tolerance to free fatty acids. However, they may experience leaching and reduced stability over time. These catalysts are particularly effective in continuous production systems [62–64].

Enzymes are protein-based biocatalysts derived from tissues, plants and microorganisms such as yeast, microbes and fungi. They are highly selective, efficient and eco-friendly, and they find applications across industries, including biofuel production, dairy, cooking, detergents, leather, paper and textiles [34,55].

Advances in enzyme immobilisation have addressed many challenges associated with enzymatic instability, particularly in industrial-scale applications. Techniques such as immobilising enzymes on nanoparticles significantly enhance their stability by increasing surface area and improving enzyme–substrate interactions. For instance, lipases immobilised on magnetite nanoparticles have demonstrated higher catalytic efficiency, thermal stability and reusability than free enzymes [12,65,66]. Cross-linked enzyme aggregates and microwave-assisted immobilisation methods enhance enzyme activity by stabilising their structure and preventing denaturation under extreme conditions.

Additionally, using ionic liquids (ILs) as co-catalysts with immobilised enzymes improves mass transfer efficiency while reducing the toxicity associated with organic solvents. ILs have been shown to increase biodiesel yields by facilitating substrate–solvent interactions, with hydrophobic ILs yielding superior performance [67]. For example, Candida antarctica lipase B immobilised with 1-hexadecyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide IL exhibited a catalytic activity of 245.13 U/g, significantly surpassing conventional solvent systems [68]. These advancements make enzymatic biodiesel production a promising eco-friendly alternative to traditional methods, with ongoing research to further reduce material costs and improve large-scale applicability.

Nanotechnology improves reaction efficiency through materials with high surface areas and reactivity [69,70]. Nanocatalysts mitigate saponification, providing a scalable alternative to conventional catalysts [71]. Their use in biodiesel production has demonstrated enhanced yields and reduced energy consumption [70–72].

The effectiveness of different transesterification methods, including their associated biodiesel yields, is summarised in Table 2.

Table 2. Biodiesel yields from different transesterification processes of microalgal oils (laboratory and pilot-scale data).

Process Algal species Catalyst Solvent Biodiesel yield
(%)
Ref.
Non-catalytic Chlorella protothecoides - Supercritical methanol 95.5 [73]
Schizochytrium limacinum - Supercritical dimethyl carbonate 50 [74]
Nannochloris sp - Supercritical methanol 21.8 [75]
Spirulina sp. - Supercritical methanol 72 [76]
Chlorella protothecoides - Supercritical ethanol 88 [77]
Homogeneous catalytic Neochloris oleoabundans NaOH Methanol 83.8 [78]
Chlorella sp. BDUG 91771 H2SO4 Methanol 60 [79]
Chlorella vulgaris KOH Methanol 90.4 [80]
Nannochloropsis gaditana HCl in methanol/chloroform Methanol >90 [81]
Heterogeneous catalytic Chlorella vulgaris KOH/Al2O3 Methanol 89.5 [82]
Chlorella protothecoides CaO/dolomite Methanol >90 [83]
Scenedesmus quadricauda Cobalt-doped CaO Methanol 98 [84]
Scenedesmus obliquus WO3/ZrO2 Methanol 94.6 [15]
Nannochloropsis oculata CaMgO/Al2O3 Methanol 85.3 [85]
Scenedesmus obliquus Cr-Al mixed oxide Methanol 98.3 [86]
Biocatalytic Chlorella protothecoides Immobilised lipase Candida sp. 99-125 Methanol/water 98.2 [87]
Neochloris oleoabundans Plant-based ferric oxide - 86 [88]
Chlorella pyrenoidosa [BMIM][PF6]/Penicillium expansum lipase CAL - 90.7 [89]
Chlorella vulgaris [C16mim][NTf2] and [Bmim][Cl]/CAL B - 100 [90]
Nitzschia punctata Cladosporium tenuissimum lipase - 87.2 [91]
Nanocatalytic C. vulgaris ESP-31 Burkholderia sp. C20, immobilised on nanocomposite Fe3O4–SiO2 Methanol/hexane 95.1 [92]
Tetraselmis indica Nano-Ca(OCH3)2 - 99 [71]
Tetraselmis indica Nanocatalyst LIICO (lithium-ion–impregnated CaO) - 93 [71]
Chlorella vulgaris Immobilised Rhizopus oryzae lipase (ROL) on superparamagnetic iron NP - 68.8 [93]
Chlorella vulgaris Nano-CaO Methanol - [94]
Neochloris oleoabundans Nano-Fe2O3 Methanol 86 [70]
Spirulina sp. Nano-Ca(OCH3)2 Methanol 99 [95]
Ulva lactuca Si/ZnO Methanol 97.3 [96]

Emerging challenges and opportunities

While these methods have advanced biodiesel production, challenges such as high energy consumption, catalyst deactivation and process scalability remain [97]. Future research should prioritise integrating these technologies into cost-effective and environmentally sustainable systems to address these constraints.

Challenges and future prospects

The global reliance on fossil fuels underscores the urgency of transitioning to sustainable energy sources that align with existing infrastructure. Biodiesel, as a renewable transport biofuel, offers compatibility with current systems and a significantly reduced carbon footprint, making it a promising alternative to conventional diesel [97]. However, large-scale adoption of microalgal biodiesel faces critical challenges that require innovative solutions [98,99].

Life cycle assessment and sustainability metrics

Life cycle analysis plays a pivotal role in assessing the environmental impact of algal biofuels [100]. Key parameters include the NER, greenhouse gas emissions, water usage and waste generation. Microalgal biodiesel currently achieves an NER of approximately 2.5, which is lower than the NER of 5 for fossil diesel. This gap highlights the importance of energy-efficient cultivation, harvesting and processing techniques to improve sustainability and economic feasibility [101].

The role of nanotechnology

Nanotechnology offers innovative solutions to overcome technical and economic barriers in microalgae-based biodiesel production. Nanocatalysts, such as nano-CaO derived from low-cost materials, exhibit high reusability, enhanced reaction rates and biodiesel yields exceeding 99%. By improving these processes, nanotechnology supports sustainability targets identified in life cycle assessment studies and cost reduction goals, positioning it as a critical enabler for commercialisation [100].

Strategies for commercialisation

Future strategies must focus on integrating microalgae biorefineries with other industries to achieve commercial viability. Co-extraction of high-value bioproducts, such as proteins, pigments and bioplastics, can enhance profitability while supporting a circular bioeconomy. Additional measures include leveraging rural areas for low-cost cultivation, integrating aquaculture to create synergies, and using wastewater as a nutrient source to lower operational costs and reduce environmental impact [102]. For example, integrated aquaculture–algae systems in Asia (e.g. shrimp farms in Thailand) have successfully applied nutrient-rich effluent to algal growth, demonstrating how nutrient recycling can lower feed costs and improve water quality [103,104].

Despite significant laboratory progress, large-scale deployment of microalgal biodiesel remains constrained by cost and scalability barriers. Techno-economic assessments estimate current production costs at approximately US$4–6 per litre, driven by energy demands for cultivation, harvesting and lipid extraction [105]. Recent pilot-scale studies integrating wastewater-based cultivation, nutrient recycling and automated PBR controls have demonstrated potential cost reductions in 20–30% [106]. These insights directly connect technological innovation to industrial feasibility, underscoring the need for aligned research and policy frameworks.

Carbon trading and economic incentives

The ability of microalgae to sequester carbon dioxide and produce secondary products positions them as an attractive option for carbon trading. High-value bioproducts, including fatty acids, vitamins and pigments, offer economic incentives for energy companies, potentially accelerating investments in algae-based biofuels [107–110]. For instance, Algenol biofuels (Florida, U.S.A.) demonstrated CO₂ utilisation by recycling industrial emissions into algal cultivation, illustrating how such systems could integrate with carbon credit frameworks to incentivise large-scale adoption [111]. In addition, the US EPA recognised Algenol’s platform for integrating CO₂ utilisation with co-production of valuable pigments and biofuels, providing a model for scalable biorefineries [104].

Research priorities

Future research must prioritise innovative farming techniques, such as automated and precision-based cultivation, to optimise productivity and scalability. Developing genetically modified strains tailored for industrial-scale production and metabolic pathway optimisation can further boost lipid yields and resource efficiency. Moreover, emphasis on reducing energy inputs across all stages, from cultivation to conversion, remains essential to align with life cycle targets and ensure economic feasibility [112].

Recent AI and machine learning advances are accelerating microalgal strain development and process optimisation. Machine learning models have achieved predictive accuracies exceeding 90% for lipid productivity by integrating cultivation parameters such as nutrient levels, light intensity and pH [113]. A random forest approach has demonstrated 95.2% accuracy in optimising lipid productivity in Chlorella sp. by balancing biomass productivity and lipid content, identifying iron and phosphorus availability as key drivers over traditional nitrogen starvation strategies [114]. Similarly, deep learning and hybrid algorithms have been applied to optimise PBR conditions, enabling in silico fine-tuning of CO₂ flux, illumination and mixing regimes before experimental validation, improving lipid yields while reducing operational costs [115]. AI-driven metabolic modelling has also highlighted gene targets for CRISPR-based enhancement, reducing iterative experimentation. By integrating AI with omics data and automated high-throughput screening, these approaches offer a scalable framework to shorten development timelines, improve resource efficiency and bridge the gap between laboratory innovation and industrial implementation [113,115].

In summary, addressing these challenges through interdisciplinary research, technological innovation and policy support will be crucial for realising the economic and environmental benefits of microalgae-based biodiesel. With continued progress, microalgae biorefineries have the potential to play a transformative role in the global energy transition.

Summary.

  • Microalgae as a sustainable biodiesel feedstock: microalgae offer high lipid productivity, rapid growth and the ability to grow in non-arable land and wastewater, positioning them as a cornerstone of third- and fourth-generation biofuels.

  • Advances in technology: recent developments in genetic engineering, nanotechnology, AI-driven strain optimisation and hybrid cultivation systems have significantly improved biodiesel yields and process efficiency.

  • Integration into biorefineries: co-production of high-value bioproducts (pigments, proteins and nutraceuticals) enhances economic viability and supports circular bioeconomy models.

  • Remaining challenges: high energy costs, scalability constraints and limited industrial deployment remain barriers; life cycle assessments (net energy ratio ~2.5) highlight areas for improvement.

  • Future directions: to transition microalgal biodiesel from laboratory to commercial reality, it is essential to focus on techno-economic optimisation, pilot-scale demonstrations and supportive policy frameworks.

Conclusion

Microalgae hold immense promise as a sustainable feedstock for biodiesel production, addressing both environmental and energy challenges. Their ability to thrive in diverse environments, including non-arable land and wastewater, with high lipid productivity and rapid growth, positions them as a leading candidate for third- and fourth-generation biodiesel, reducing dependence on fossil fuels and mitigating climate change impacts.

Future work should prioritise pilot-scale demonstrations that validate laboratory innovations under industrial conditions, including automated PBR controls and wastewater-integrated cultivation systems to reduce costs. Research into strain engineering via CRISPR-Cas9 and AI-driven process optimisation should be coupled with techno-economic modelling to guide scale-up. By integrating AI, CRISPR and nanotechnology with sustainability insights, microalgal biodiesel can advance beyond laboratory constraints toward commercial viability.

Policy measures, such as carbon credit incentives for CO₂ biofixation, feed-in tariffs for algae-derived fuels and nutrient recycling regulations, alongside collaboration between academia, industry and government, will be critical to aligning research breakthroughs with infrastructure and market development. The co-production of high-value bioproducts also strengthens the feasibility of microalgae biorefineries within a circular bioeconomy.

Despite decades of research, algal biodiesel remains commercially unrealised. Production costs (US$4–6/l) exceed fossil diesel pricing, NERs remain suboptimal (NER ~2.5 vs. ~5 for fossil diesel), and large-scale cultivation faces contamination and infrastructure challenges. Highly variable life cycle assessments further limit definitive sustainability claims. As a result, most efforts have shifted toward high-value co-products rather than bulk fuel. Demonstrating cost competitiveness and sustainability will require integrated techno-economic optimisation, validated pilot-scale data and targeted policy support to close the gap between laboratory advances and industrial feasibility.

Abbreviations

AI

artificial intelligence

CaO

calcium oxide

FAMEs

fatty acid methyl esters

GEM

genetically engineered microalgae

ILs

ionic liquids

NER

net energy ratio

PBR

photobioreactor

Contributor Information

Fariha Kanwal, Email: farihakanwal2021@gmail.com.

Ambreen Aslam, Email: ambreenaslam86@hotmail.com.

Dr Angel A. J. Torriero, Email: angel.torriero@deakin.edu.au.

Competing Interests

The authors declare that there are no competing interests associated with the manuscript.

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References

  • 1. Hassan Q., Viktor P., J. Al-Musawi T., Mahmood Ali B., Algburi S., Alzoubi H.M., et al. The renewable energy role in the global energy Transformations. Renewable Energy Focus. 2024;48:100545. doi: 10.1016/j.ref.2024.100545. [DOI] [Google Scholar]
  • 2. Zhang S., Zhang L., Xu G., Li F., Li X A review on biodiesel production from microalgae: Influencing parameters and recent advanced technologies. Front. Microbiol. 2022;13 doi: 10.3389/fmicb.2022.970028. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3. Benti N.E., Aneseyee A.B., Geffe C.A., Woldegiyorgis T.A., Gurmesa G.S., Bibiso M., et al. Biodiesel production in ethiopia: current status and future prospects. Scientific African. 2023;19:e01531. doi: 10.1016/j.sciaf.2022.e01531. [DOI] [Google Scholar]
  • 4. Nisar A., Hashum K., Bashir M., Mubeen N., Younus S., Mehmood S., H., et al. Advancing Sustainable Biofuel Production from Agricultural Residues: a Comprehensive Mini-Review. SCE. :116–129. doi: 10.37256/sce.5120243763. [DOI] [Google Scholar]
  • 5. Roser M2023) Ensure access to affordable, reliable, sustainable and modern energy for all https://ourworldindata.org/sdgs/affordable-clean-energy
  • 6. Zhang M., Liu J., Wang Y., Yu B., Wu X., Qiang Z., et al. Morphologically-different cells and colonies cause distinctive performance of coagulative colloidal ozone microbubbles in simultaneously removing bloom-forming cyanobacteria and microcystin-LR. J. Hazard. Mater. 2022;435:128986. doi: 10.1016/j.jhazmat.2022.128986. [DOI] [PubMed] [Google Scholar]
  • 7. Dey S., Reang N.M., Das P.K., Deb M A comprehensive study on prospects of economy, environment, and efficiency of palm oil biodiesel as a renewable fuel. J. Clean. Prod. 2021;286:124981. doi: 10.1016/j.jclepro.2020.124981. [DOI] [Google Scholar]
  • 8. Liu Y., Cruz-Morales P., Zargar A., Belcher M.S., Pang B., Englund E, et al. Biofuels for a sustainable future. Cell. 2021;184:1636–1647. doi: 10.1016/j.cell.2021.01.052. [DOI] [PubMed] [Google Scholar]
  • 9. Li G., Zhang J., Li H., Hu R., Yao X., Liu Y., et al. Towards high-quality biodiesel production from microalgae using original and anaerobically-digested livestock wastewater. Chemosphere. 2021;273:128578. doi: 10.1016/j.chemosphere.2020.128578. [DOI] [PubMed] [Google Scholar]
  • 10. Pandey S., Narayanan I., Selvaraj R., Varadavenkatesan T., Vinayagam R Biodiesel production from microalgae: a comprehensive review on influential factors, transesterification processes, and challenges. Fuel (Lond). 2024;367:131547. doi: 10.1016/j.fuel.2024.131547. [DOI] [Google Scholar]
  • 11. Khoo K.S., Ahmad I., Chew K.W., Iwamoto K., Bhatnagar A., Show P.L Enhanced microalgal lipid production for biofuel using different strategies including genetic modification of microalgae: A review. Prog. Energy Combust. Sci. 2023;96:101071. doi: 10.1016/j.pecs.2023.101071. [DOI] [Google Scholar]
  • 12. Mota G.F., Sousa I. G. , De Oliveira A.L.B., De Cavalcante A.L.G., Da Moreira K.S., Cavalcante F. T. T, et al. Biodiesel production from microalgae using lipase-based catalysts: current challenges and prospects. Algal Res. 2022;62:102616. doi: 10.1016/j.algal.2021.102616. [DOI] [Google Scholar]
  • 13. Faruque M.O., Razzak S.A., Hossain M.M Application of Heterogeneous Catalysts for Biodiesel Production from Microalgal Oil—A Review. Catalysts. 2020;10:1025. doi: 10.3390/catal10091025. [DOI] [Google Scholar]
  • 14. Brindhadevi K., Mathimani T., Rene E.R., Shanmugam S., Chi N.T.L., Pugazhendhi A Impact of cultivation conditions on the biomass and lipid in microalgae with an emphasis on biodiesel. Fuel (Lond). 2021;284:119058. doi: 10.1016/j.fuel.2020.119058. [DOI] [Google Scholar]
  • 15. Guldhe A., Singh P., Ansari F.A., Singh B., Bux F Biodiesel synthesis from microalgal lipids using tungstated zirconia as a heterogeneous acid catalyst and its comparison with homogeneous acid and enzyme catalysts. Fuel (Lond). 2017;187:180–188. doi: 10.1016/j.fuel.2016.09.053. [DOI] [Google Scholar]
  • 16. (2021. a) The dynamic effect of micro-structural shocks on private investment behavior AMS 1–17. 10.46544/AMS.v26i1.01 [DOI] [Google Scholar]
  • 17. (2021. b) The analysis of investment into industries based on portfolio managers AMS 161–170. 10.46544/AMS.v26i1.14 33425351 [DOI] [Google Scholar]
  • 18. Chhandama M.V.L., Satyan K.B., Changmai B., Vanlalveni C., Rokhum S.L Microalgae as a feedstock for the production of biodiesel: A review. Bioresource Technology Reports. 2021;15:100771. doi: 10.1016/j.biteb.2021.100771. [DOI] [Google Scholar]
  • 19. Hawrot-Paw M., Ratomski P., Koniuszy A., Golimowski W., Teleszko M., Grygier A Fatty acid profile of microalgal oils as a criterion for selection of the best feedstock for biodiesel production. Energies. 2021;14:7334. doi: 10.3390/en14217334. [DOI] [Google Scholar]
  • 20. Valério A., Vieitez I., Matos Â.P., Oliveira J.V2024Lipids and Fatty Acids from MicroalgaeInIn Microalgal Bioengineeringpp247–280.Springer; 10.1007/978-3-031-61253-4_11 [DOI] [Google Scholar]
  • 21. Ananthi V., Raja R., Carvalho I.S., Brindhadevi K., Pugazhendhi A., Arun A A realistic scenario on microalgae based biodiesel production: Third generation biofuel. Fuel (Lond). 2021;284:118965. doi: 10.1016/j.fuel.2020.118965. [DOI] [Google Scholar]
  • 22. Ori M.O., Ekpan F.-D.M., Samuel H.S., Egwuatu O.P Emerging Co-Cultivation Strategies for Microalgal Biomass and Biodiesel Production. Progress in Chemical and Biochemical Research. 2024;7:198–224. doi: 10.48309/pcbr.2024.425990.1317. [DOI] [Google Scholar]
  • 23. Tang D.Y.Y., Yew G.Y., Koyande A.K., Chew K.W., Vo D.-V.N., Show P.L Green technology for the industrial production of biofuels and bioproducts from microalgae: a review. Environ. Chem. Lett. 2020;18:1967–1985. doi: 10.1007/s10311-020-01052-3. [DOI] [Google Scholar]
  • 24. Lang I., Hodac L., Friedl T., Feussner I Fatty acid profiles and their distribution patterns in microalgae: a comprehensive analysis of more than 2000 strains from the SAG culture collection. BMC Plant Biol. 2011;11:124. doi: 10.1186/1471-2229-11-124. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25. Eldiehy K.S.H., Bardhan P., Borah D., Gohain M., Ahmad Rather M., Deka D., et al. A comprehensive review on microalgal biomass production and processing for biodiesel production. Fuel (Lond). 2022;324:124773. doi: 10.1016/j.fuel.2022.124773. [DOI] [Google Scholar]
  • 26. Abdullah M., Ali Z., Yasin M.T., Amanat K., Sarwar F., Khan J, et al. Advancements in sustainable production of biofuel by microalgae: recent insights and future directions. Environ. Res. 2024;262:119902. doi: 10.1016/j.envres.2024.119902. [DOI] [PubMed] [Google Scholar]
  • 27. Raut N., Al-Balushi T., Panwar S., Vaidya R., Shinde G Microalgal biofuel. Biofuels-Status and Perspective. 2015:101–140. doi: 10.5772/59821. [DOI] [Google Scholar]
  • 28. Show P.L., Tang M.S.Y., Nagarajan D., Ling T.C., Ooi C.-W., Chang J.-S A holistic approach to managing microalgae for biofuel applications. Int. J. Mol. Sci. 2017;18:215. doi: 10.3390/ijms18010215. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29. Deshmukh S., Kumar R., Bala K Microalgae biodiesel: A review on oil extraction, fatty acid composition, properties and effect on engine performance and emissions. Fuel Processing Technology. 2019;191:232–247. doi: 10.1016/j.fuproc.2019.03.013. [DOI] [Google Scholar]
  • 30. Xiao M., Shin H.-J., Dong Q Advances in cultivation and processing techniques for microalgal biodiesel: a review. Korean J. Chem. Eng. 2013;30:2119–2126. doi: 10.1007/s11814-013-0161-1. [DOI] [Google Scholar]
  • 31. Udayan A., Pandey A.K., Sirohi R., Sreekumar N., Sang B.-I., Sim S.J., et al. Production of microalgae with high lipid content and their potential as sources of nutraceuticals. Phytochem. Rev. 2023;22:833–860. doi: 10.1007/s11101-021-09784-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32. Mandotra S.K., Kumar P., Suseela M.R., Nayaka S., Ramteke P.W Evaluation of fatty acid profile and biodiesel properties of microalga Scenedesmus abundans under the influence of phosphorus, pH and light intensities. Bioresour. Technol. 2016;201:222–229. doi: 10.1016/j.biortech.2015.11.042. [DOI] [PubMed] [Google Scholar]
  • 33. Jung J.-M., Kim J.Y., Jung S., Choi Y.-E., Kwon E.E Quantitative study on lipid productivity of Euglena gracilis and its biodiesel production according to the cultivation conditions. J. Clean. Prod. 2021;291:125218. doi: 10.1016/j.jclepro.2020.125218. [DOI] [Google Scholar]
  • 34. Kim J.Y., Jung J.M., Jung S., Park Y.K., Tsang Y.F., Lin K.Y.A., et al. Biodiesel from microalgae: Recent progress and key challenges. Prog. Energy Combust. Sci. 2022;93:101020. doi: 10.1016/j.pecs.2022.101020. [DOI] [Google Scholar]
  • 35. Ma Y., Wang Z., Yu C., Yin Y., Zhou G Evaluation of the potential of 9 Nannochloropsis strains for biodiesel production. Bioresour. Technol. 2014;167:503–509. doi: 10.1016/j.biortech.2014.06.047. [DOI] [PubMed] [Google Scholar]
  • 36. Razzak S.A., Lucky R.A., Hossain M.M., deLasa H Valorization of microalgae biomass to biofuel production: a review. Energy Nexus. 2022;7:100139. doi: 10.1016/j.nexus.2022.100139. [DOI] [Google Scholar]
  • 37. Menegazzo M.L., Fonseca G.G Biomass recovery and lipid extraction processes for microalgae biofuels production: A review. Renewable and Sustainable Energy Reviews. 2019;107:87–107. doi: 10.1016/j.rser.2019.01.064. [DOI] [Google Scholar]
  • 38. Rodríguez-Palacio M.C., Cabrera-Cruz R.B.E., Rolón-Aguilar J.C., Tobías-Jaramillo R., Martínez-Hernández M., Lozano-Ramírez C The cultivation of five microalgae species and their potential for biodiesel production. Energy. Sustain. Soc. 2022;12:10. doi: 10.1186/s13705-022-00337-5. [DOI] [Google Scholar]
  • 39. Prado L. de O., Bolzani H.R., Souza H.H. de S., Ruas G., Da Silva G.H.R Microalgal cultivation in open and closed systems under a tropical climate: A life cycle comparison. J. Clean. Prod. 2023;422:138631. doi: 10.1016/j.jclepro.2023.138631. [DOI] [Google Scholar]
  • 40. Isiramen O.E., Bahri P.A., Moheimani N.R., Vadiveloo A., Shayesteh H., Parlevliet D.A Improving pH control and carbon dioxide utilisation efficiency in microalgae cultivation systems with the use of a Proportional-integral + dead-zone control strategy. Bioresource Technology Reports. 2022;17:100917. doi: 10.1016/j.biteb.2021.100917. [DOI] [Google Scholar]
  • 41. Veeramuthu A., Ngamcharussrivichai C2020Potential of microalgal biodiesel: challenges and applicationsInIn Renewable Energy-Technologies and Applications Taner T., Tiwari A., Ustun T.S., eds), , 10.5772/intechopen.91651 [DOI] [Google Scholar]
  • 42. Chowdury K.H., Nahar N., Deb U.K The growth factors involved in microalgae cultivation for biofuel production: a review. CWEEE. 2020;09:185–215. doi: 10.4236/cweee.2020.94012. [DOI] [Google Scholar]
  • 43. Fabris M., Abbriano R.M., Pernice M., Sutherland D.L., Commault A.S., Hall C.C., et al. Emerging technologies in algal biotechnology: toward the establishment of a sustainable, algae-based bioeconomy. Front. Plant Sci. 2020;11 doi: 10.3389/fpls.2020.00279. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 44. Ganesan R., Manigandan S., Samuel M.S., Shanmuganathan R., Brindhadevi K., Lan Chi N.T., et al. A review on prospective production of biofuel from microalgae. Biotechnol. Rep. (Amst). 2020;27:e00509. doi: 10.1016/j.btre.2020.e00509. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 45. Roy M., Mohanty K A comprehensive review on microalgal harvesting strategies: Current status and future prospects. Algal Res. 2019;44:101683. doi: 10.1016/j.algal.2019.101683. [DOI] [Google Scholar]
  • 46. Kumari N., Singh R.K Biofuel and co-products from algae solvent extraction. J. Environ. Manage. 2019;247:196–204. doi: 10.1016/j.jenvman.2019.06.042. [DOI] [PubMed] [Google Scholar]
  • 47. Gorgich M., Mata T.M., Martins A.A., Branco-Vieira M., Caetano N.S Comparison of different lipid extraction procedures applied to three microalgal species. Energy Reports. 2020;6:477–482. doi: 10.1016/j.egyr.2019.09.011. [DOI] [Google Scholar]
  • 48. Bhargavi G., Nageswara Rao P., Renganathan S Review on the extraction methods of crude oil from all generation biofuels in last few decades. IOP Conf. Ser.: Mater. Sci. Eng. 2018;330:012024. doi: 10.1088/1757-899X/330/1/012024. [DOI] [Google Scholar]
  • 49. Patel A., Matsakas L., Sartaj K., Chandra R2020Chapter 2 - Extraction of lipids from algae using supercritical carbon dioxideInIn Green Sustainable Process for Chemical and Environmental Engineering and Science (Inamuddin Asiri A.M., Isloor A.M.edspp17–39.Elsevier; [Google Scholar]
  • 50. Pikula K., Zakharenko A., Stratidakis A., Razgonova M., Nosyrev A., Mezhuev Y., et al. The advances and limitations in biodiesel production: feedstocks, oil extraction methods, production, and environmental life cycle assessment. Green Chemistry Letters and Reviews. 2020;13:275–294. doi: 10.1080/17518253.2020.1829099. [DOI] [Google Scholar]
  • 51. Batista F.R.M., Lucchesi K.W., Carareto N.D.D., Costa M.C.D., Meirelles A.J.A Properties of microalgae oil from the species chlorella protothecoides and its ethylic biodiesel. Braz. J. Chem. Eng. 2018;35:1383–1394. doi: 10.1590/0104-6632.20180354s20170191. [DOI] [Google Scholar]
  • 52. Neag E., Stupar Z., Maicaneanu S.A., Roman C Advances in biodiesel production from microalgae. Energies. 2023;16:1129. doi: 10.3390/en16031129. [DOI] [Google Scholar]
  • 53. Felix C., Ubando A., Madrazo C., Gue I.H., Sutanto S., Tran-Nguyen P.L., et al. Non-catalytic in-situ (trans) esterification of lipids in wet microalgae Chlorella vulgaris under subcritical conditions for the synthesis of fatty acid methyl esters. Appl. Energy. 2019;248:526–537. doi: 10.1016/j.apenergy.2019.04.149. [DOI] [Google Scholar]
  • 54. Zhang Y., Li Y., Zhang X., Tan T Biodiesel production by direct transesterification of microalgal biomass with co-solvent. Bioresour. Technol. 2015;196:712–715. doi: 10.1016/j.biortech.2015.07.052. [DOI] [PubMed] [Google Scholar]
  • 55. Vijayalakshmi S., Anand M., Ranjitha J2020Chapter 16 - Microalgae-Based Biofuel Production Using Low-Cost NanobiocatalystsInIn Microalgae Cultivation for Biofuels Production (Yousufpp251–263.Academic Press; [Google Scholar]
  • 56. Cheng J., Guo H., Yang X., Mao Y., Qian L., Zhu Y., et al. Phosphotungstic acid-modified zeolite imidazolate framework (ZIF-67) as an acid-base bifunctional heterogeneous catalyst for biodiesel production from microalgal lipids. Energy Convers. Manag. 2021;232:113872. doi: 10.1016/j.enconman.2021.113872. [DOI] [Google Scholar]
  • 57. Dong T., Wang J., Miao C., Zheng Y., Chen S Two-step in situ biodiesel production from microalgae with high free fatty acid content. Bioresour. Technol. 2013;136:8–15. doi: 10.1016/j.biortech.2013.02.105. [DOI] [PubMed] [Google Scholar]
  • 58. Martinez-Guerra E., Gude V.G., Mondala A., Holmes W., Hernandez R Extractive-transesterification of algal lipids under microwave irradiation with hexane as solvent. Bioresour. Technol. 2014;156:240–247. doi: 10.1016/j.biortech.2014.01.026. [DOI] [PubMed] [Google Scholar]
  • 59. Dianursanti R.P., Wijanarko A Utilization of n-Hexane as Co-solvent to Increase Biodiesel Yield on Direct Transesterification Reaction from Marine Microalgae. Procedia Environ. Sci. 2015;23:412–420. doi: 10.1016/j.proenv.2015.01.059. [DOI] [Google Scholar]
  • 60. Sivaramakrishnan R., Incharoensakdi A Production of methyl ester from two microalgae by two-step transesterification and direct transesterification. Environ. Sci. Pollut. Res. Int. 2017;24:4950–4963. doi: 10.1007/s11356-016-8217-5. [DOI] [PubMed] [Google Scholar]
  • 61. Mandari V., Devarai S.K Biodiesel Production Using Homogeneous, Heterogeneous, and Enzyme Catalysts via Transesterification and Esterification Reactions: a Critical Review. Bioenergy Res. 2022;15:935–961. doi: 10.1007/s12155-021-10333-w. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 62. Zuorro A., García-Martínez J.B., Barajas-Solano A.F The application of catalytic processes on the production of algae-based biofuels: a review. Catalysts. 2021;11:22. doi: 10.3390/catal11010022. [DOI] [Google Scholar]
  • 63. Jafari A., Esmaeilzadeh F., Mowla D., Sadatshojaei E., Heidari S., Wood D.A New insights to direct conversion of wet microalgae impregnated with ethanol to biodiesel exploiting extraction with supercritical carbon dioxide. Fuel (Lond). 2021;285:119199. doi: 10.1016/j.fuel.2020.119199. [DOI] [Google Scholar]
  • 64. Kazemifard S., Nayebzadeh H., Saghatoleslami N., Safakish E Application of magnetic alumina-ferric oxide nanocatalyst supported by KOH for in-situ transesterification of microalgae cultivated in wastewater medium. Biomass and Bioenergy. 2019;129:105338. doi: 10.1016/j.biombioe.2019.105338. [DOI] [Google Scholar]
  • 65. Bušić A., Kundas S., Morzak G., Belskaya H., Marđetko N., Ivančić Šantek M., et al. Recent trends in biodiesel and biogas production. Food Technol. Biotechnol. 2018;56:152–173. doi: 10.17113/ftb.56.02.18.5547. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 66. Piligaev A.V., Sorokina K.N., Samoylova Y.V., Parmon V.N Lipid production by microalga Micractinium sp. IC-76 in a flat panel photobioreactor and its transesterification with cross-linked enzyme aggregates of Burkholderia cepacia lipase. Energy Convers. Manag. 2018;156:1–9. doi: 10.1016/j.enconman.2017.10.086. [DOI] [Google Scholar]
  • 67. Ong H.C., Tiong Y.W., Goh B.H.H., Gan Y.Y., Mofijur M., Fattah I.M.R., et al. Recent advances in biodiesel production from agricultural products and microalgae using ionic liquids: Opportunities and challenges. Energy Convers. Manag. 2021;228:113647. doi: 10.1016/j.enconman.2020.113647. [DOI] [Google Scholar]
  • 68. De Diego T., Manjón A., Lozano P., Vaultier M., Iborra J.L An efficient activity ionic liquid-enzyme system for biodiesel production. Green Chem. 2011;13:444. doi: 10.1039/c0gc00230e. [DOI] [Google Scholar]
  • 69. Kazemi Shariat Panahi H., Hosseinzadeh-Bandbafha H., Dehhaghi M., Orooji Y., Mahian O., Shahbeik H., et al. Nanotechnology applications in biodiesel processing and production: A comprehensive review. Renewable and Sustainable Energy Reviews. 2024;192:114219. doi: 10.1016/j.rser.2023.114219. [DOI] [Google Scholar]
  • 70. Banerjee S., Rout S., Banerjee S., Atta A., Das D Fe2O3 nanocatalyst aided transesterification for biodiesel production from lipid-intact wet microalgal biomass: A biorefinery approach. Energy Convers. Manag. 2019;195:844–853. doi: 10.1016/j.enconman.2019.05.060. [DOI] [Google Scholar]
  • 71. Mittal V., Kumar Ghosh U Comparative analysis of two different nanocatalysts for producing biodiesel from microalgae. Mater. Today. 2022;63:515–519. doi: 10.1016/j.matpr.2022.03.652. [DOI] [Google Scholar]
  • 72. Akubude V.C., Nwaigwe K.N., Dintwa E Production of biodiesel from microalgae via nanocatalyzed transesterification process: A review. Materials Science for Energy Technologies. 2019;2:216–225. doi: 10.1016/j.mset.2018.12.006. [DOI] [Google Scholar]
  • 73. Liu J., Lin R., Nan Y., Tavlarides L.L Production of biodiesel from microalgae oil (Chlorella protothecoides) by non-catalytic transesterification: Evaluation of reaction kinetic models and phase behavior. J. Supercrit. Fluids. 2015;99:38–50. doi: 10.1016/j.supflu.2015.01.010. [DOI] [Google Scholar]
  • 74. Mani Rathnam V., Madras G Conversion of Shizochitrium limacinum microalgae to biodiesel by non-catalytic transesterification using various supercritical fluids. Bioresour. Technol. 2019;288:121538.:121538. doi: 10.1016/j.biortech.2019.121538. [DOI] [PubMed] [Google Scholar]
  • 75. Jazzar S., Quesada-Medina J., Olivares-Carrillo P., Marzouki M.N., Acién-Fernández F.G., Fernández-Sevilla J.M, et al. A whole biodiesel conversion process combining isolation, cultivation and in situ supercritical methanol transesterification of native microalgae. Bioresour. Technol. 2015;190:281–288. doi: 10.1016/j.biortech.2015.04.097. [DOI] [PubMed] [Google Scholar]
  • 76. Tobar M., Núñez G.A Supercritical transesterification of microalgae triglycerides for biodiesel production: Effect of alcohol type and co-solvent. J. Supercrit. Fluids. 2018;137:50–56. doi: 10.1016/j.supflu.2018.03.008. [DOI] [Google Scholar]
  • 77. Nan Y., Liu J., Lin R., Tavlarides L.L Production of biodiesel from microalgae oil (Chlorella protothecoides) by non-catalytic transesterification in supercritical methanol and ethanol: Process optimization. J. Supercrit. Fluids. 2015;97:174–182. doi: 10.1016/j.supflu.2014.08.025. [DOI] [Google Scholar]
  • 78. Karthikeyan S., Kalaimurugan K., Prathima A Quality analysis studies on biodiesel production of neochloris oleoabundans algae. Energy Sources, Part A: Recovery, Utilization, and Environmental Effects. 2018;40:439–445. doi: 10.1080/15567036.2017.1422059. [DOI] [Google Scholar]
  • 79. Mathimani T., Uma L., Prabaharan D Homogeneous acid catalysed transesterification of marine microalga Chlorella sp. BDUG 91771 lipid – An efficient biodiesel yield and its characterization. Renewable Energy. 2015;81:523–533. doi: 10.1016/j.renene.2015.03.059. [DOI] [Google Scholar]
  • 80. Nguyen T.T., Uemura Y., Lam M.K., Mansor N., Lim J.W Revealing the effect of reaction parameters towards alkyl group distribution in in-situ transesterification of Chlorella vulgaris. Energy Convers. Manag. 2019;185:223–231. doi: 10.1016/j.enconman.2019.01.113. [DOI] [Google Scholar]
  • 81. Kim B., Im H., Lee J.W In situ transesterification of highly wet microalgae using hydrochloric acid. Bioresour. Technol. 2015;185:421–425. doi: 10.1016/j.biortech.2015.02.092. [DOI] [PubMed] [Google Scholar]
  • 82. Ma G., Hu W., Pei H., Jiang L., Ji Y., Mu R Study of KOH/Al2O3 as heterogeneous catalyst for biodiesel production via in situ transesterification from microalgae. Environ. Technol. 2015;36:622–627. doi: 10.1080/09593330.2014.954629. [DOI] [PubMed] [Google Scholar]
  • 83. Çakırca E.E., N Tekin G., İlgen O., N Akın A Catalytic activity of CaO-based catalyst in transesterification of microalgae oil with methanol. Energy & Environment. 2019;30:176–187. doi: 10.1177/0958305X18787317. [DOI] [Google Scholar]
  • 84. Das V., Tripathi A.M., Borah M.J., Dunford N.T., Deka D Cobalt-doped CaO catalyst synthesized and applied for algal biodiesel production. Renewable Energy. 2020;161:1110–1119. doi: 10.1016/j.renene.2020.07.040. [DOI] [Google Scholar]
  • 85. Teo S.H., Taufiq-Yap Y.H., Ng F.L Alumina supported/unsupported mixed oxides of Ca and Mg as heterogeneous catalysts for transesterification of Nannochloropsis sp. microalga’s oil. Energy Convers. Manag. 2014;88:1193–1199. doi: 10.1016/j.enconman.2014.04.049. [DOI] [Google Scholar]
  • 86. Guldhe A., Moura C.V.R., Singh P., Rawat I., Moura E.M., Sharma Y., et al. Conversion of microalgal lipids to biodiesel using chromium-aluminum mixed oxide as a heterogeneous solid acid catalyst. Renewable Energy. 2017;105:175–182. doi: 10.1016/j.renene.2016.12.053. [DOI] [Google Scholar]
  • 87. Xiong W., Li X., Xiang J., Wu Q High-density fermentation of microalga Chlorella protothecoides in bioreactor for microbio-diesel production. Appl. Microbiol. Biotechnol. 2008;78:29–36. doi: 10.1007/s00253-007-1285-1. [DOI] [PubMed] [Google Scholar]
  • 88. Choudhury P., Ray R.N., Bandyopadhyay T.K., Bhunia B Fed batch approach for stable generation of power from dairy wastewater using microbial fuel cell and its kinetic study. Fuel (Lond). 2020;266:117073. doi: 10.1016/j.fuel.2020.117073. [DOI] [Google Scholar]
  • 89. Lai J.-Q., Hu Z.-L., Wang P.-W., Yang Z2012Enzymatic production of microalgal biodiesel in ionic liquid [BMIm][PF6] [PF6]Fuel (Lond). 95329–333. 10.1016/j.fuel.2011.11.001 [DOI] [Google Scholar]
  • 90. Lozano P., Bernal J.M., Gómez C., Álvarez E., Markiv B., García-Verdugo E., et al. Green biocatalytic synthesis of biodiesel from microalgae in one-pot systems based on sponge-like ionic liquids. Catal. Today. 2020;346:87–92. doi: 10.1016/j.cattod.2019.01.073. [DOI] [Google Scholar]
  • 91. Saranya G., Ramachandra T.V Novel biocatalyst for optimal biodiesel production from diatoms. Renewable Energy. 2020;153:919–934. doi: 10.1016/j.renene.2020.02.053. [DOI] [Google Scholar]
  • 92. Tran D.-T., Chen C.-L., Chang J.-S Effect of solvents and oil content on direct transesterification of wet oil-bearing microalgal biomass of Chlorella vulgaris ESP-31 for biodiesel synthesis using immobilized lipase as the biocatalyst. Bioresour. Technol. 2013;135:213–221. doi: 10.1016/j.biortech.2012.09.101. [DOI] [PubMed] [Google Scholar]
  • 93. Nematian T., Salehi Z., Shakeri A Conversion of bio-oil extracted from Chlorella vulgaris micro algae to biodiesel via modified superparamagnetic nano-biocatalyst. Renewable Energy. 2020;146:1796–1804. doi: 10.1016/j.renene.2019.08.048. [DOI] [Google Scholar]
  • 94. Davoodbasha M., Pugazhendhi A., Kim J.-W., Lee S.-Y., Nooruddin T Biodiesel production through transesterification of chlorella vulgaris: synthesis and characterization of CaO nanocatalyst. Fuel (Lond). 2021;300:121018. doi: 10.1016/j.fuel.2021.121018. [DOI] [Google Scholar]
  • 95. Mittal V., Ghosh U.K Optimization of biodiesel production from Spirulina microalgae via nanocatalytic transesterification process. Bioresource Technology Reports. 2023;23:101504. doi: 10.1016/j.biteb.2023.101504. [DOI] [Google Scholar]
  • 96. Kalavathy G., Baskar G Synergism of clay with zinc oxide as nanocatalyst for production of biodiesel from marine Ulva lactuca. Bioresour. Technol. 2019;281:234–238. doi: 10.1016/j.biortech.2019.02.101. [DOI] [PubMed] [Google Scholar]
  • 97. Kumar Das P.Prava Das B.Dash P., and In Nanomaterials (Kumar, R. P. and Bharathiraja, B., eds.). pp . 2021) Chapter 16 - Application of Nanotechnology in the Production of Bioenergy from Algal Biomass: Opportunities and Challenges Academic Press; [Google Scholar]
  • 98. Sunil Kumar M., Buddolla V2019Chapter 12 - Future Prospects of Biodiesel Production by Microalgae: A Short ReviewInIn Recent Developments in Applied Microbiology and Biochemistry (Buddollapp161–166.Academic Press; [Google Scholar]
  • 99. Gendy T.S., El-Temtamy S.A Commercialization potential aspects of microalgae for biofuel production: An overview. Egyptian Journal of Petroleum. 2013;22:43–51. doi: 10.1016/j.ejpe.2012.07.001. [DOI] [Google Scholar]
  • 100. Esmaeili H A critical review on the economic aspects and life cycle assessment of biodiesel production using heterogeneous nanocatalysts. Fuel Processing Technology. 2022;230:107224. doi: 10.1016/j.fuproc.2022.107224. [DOI] [Google Scholar]
  • 101. Ali H.E.A., El-fayoumy E.A., Soliman R.M., Elkhatat A., Al-Meer S., Elsaid K., et al. Nanoparticle applications in Algal-biorefinery for biofuel production. Renewable and Sustainable Energy Reviews. 2024;192:114267. doi: 10.1016/j.rser.2023.114267. [DOI] [Google Scholar]
  • 102. Kim B., Heo H.Y., Son J., Yang J., Chang Y.-K., Lee J.H., et al. Simplifying biodiesel production from microalgae via wet in situ transesterification: A review in current research and future prospects. Algal Res. 2019;41:101557. doi: 10.1016/j.algal.2019.101557. [DOI] [Google Scholar]
  • 103. Sarwer A., Hamed S.M., Osman A.I., Jamil F., Al-Muhtaseb A.H., Alhajeri N.S., et al. Algal biomass valorization for biofuel production and carbon sequestration: a review. Environ. Chem. Lett. 2022;20:2797–2851. doi: 10.1007/s10311-022-01458-1. [DOI] [Google Scholar]
  • 104. US EPA Green Chemistry Award - Algenol Biofuels 2015) Presidential Green Chemistry Challenge: 2015 Algenol Biofuels Award https://www.epa.gov/greenchemistry/presidential-green-chemistry-challenge-2015-specific-environmental-benefit-climate
  • 105. Maroušek J., Maroušková A., Gavurová B., Tuček D., Strunecký O Competitive algae biodiesel depends on advances in mass algae cultivation. Bioresour. Technol. 2023;374:128802. doi: 10.1016/j.biortech.2023.128802. [DOI] [PubMed] [Google Scholar]
  • 106. Zewdie D.T., Ali A.Y Techno-economic analysis of microalgal biofuel production coupled with sugarcane processing factories. South African Journal of Chemical Engineering. 2022;40:70–79. doi: 10.1016/j.sajce.2022.01.006. [DOI] [Google Scholar]
  • 107. Cai W., Wang L., Li L., Xie J., Jia S., Zhang X., et al. A review on methods of energy performance improvement towards sustainable manufacturing from perspectives of energy monitoring, evaluation, optimization and benchmarking. Renewable and Sustainable Energy Reviews. 2022;159:112227. doi: 10.1016/j.rser.2022.112227. [DOI] [Google Scholar]
  • 108. Gourvenec S., Sturt F., Reid E., Trigos F Global assessment of historical, current and forecast ocean energy infrastructure: Implications for marine space planning, sustainable design and end-of-engineered-life management. Renewable and Sustainable Energy Reviews. 2022;154:111794. doi: 10.1016/j.rser.2021.111794. [DOI] [Google Scholar]
  • 109. Chen J., Tyagi R.D., Li J., Zhang X., Drogui P., Sun F Economic assessment of biodiesel production from wastewater sludge. Bioresour. Technol. 2018;253:41–48. doi: 10.1016/j.biortech.2018.01.016. [DOI] [PubMed] [Google Scholar]
  • 110. Chong J.W.R., Khoo K.S., Chew K.W., Ting H.Y., Show P.L Trends in digital image processing of isolated microalgae by incorporating classification algorithm. Biotechnol. Adv. 2023;63:108095. doi: 10.1016/j.biotechadv.2023.108095. [DOI] [PubMed] [Google Scholar]
  • 111. Algenol Biofuels 2024) Algenol Biofuels https://www.algenol.com
  • 112. Hossain N., Mahlia T.M.I Progress in physicochemical parameters of microalgae cultivation for biofuel production. Crit. Rev. Biotechnol. 2019;39:835–859. doi: 10.1080/07388551.2019.1624945. [DOI] [PubMed] [Google Scholar]
  • 113. Coşgun A., Günay M.E., Yıldırım R Machine learning for algal biofuels: a critical review and perspective for the future. Green Chem. 2023;25:3354–3373. doi: 10.1039/D3GC00389B. [DOI] [Google Scholar]
  • 114. Lopez A.M., Savage S., Zhou Z Novel machine learning unlocks high lipid productivity and resolves trade-offs in algal biofuel production. Renewable Energy. 2026;256:123901. doi: 10.1016/j.renene.2025.123901. [DOI] [Google Scholar]
  • 115. Imamoglu E Artificial intelligence and/or machine learning algorithms in microalgae bioprocesses. Bioengineering (Basel). 2024;11:1143. doi: 10.3390/bioengineering11111143. [DOI] [PMC free article] [PubMed] [Google Scholar]

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