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Review

Beyond Bioremediation: The Untapped Potential of Microalgae in Wastewater Treatment

1
Centre of Marine Sciences, University of Algarve, Campus de Gambelas, 8005-139 Faro, Portugal
2
Green Colab—Associação Oceano Verde, University of Algarve, Campus de Gambelas, 8005-139 Faro, Portugal
*
Author to whom correspondence should be addressed.
Water 2024, 16(19), 2710; https://doi.org/10.3390/w16192710
Submission received: 31 July 2024 / Revised: 17 September 2024 / Accepted: 20 September 2024 / Published: 24 September 2024
(This article belongs to the Special Issue Persistent and Emerging Organic Contaminants in Natural Environments)

Abstract

:
Microalgae-based wastewater bioremediation has emerged as a promising and sustainable solution for water purification by harnessing the natural ability of microalgae to absorb and transform pollutants. In the literature, it is possible to find diverse microalgae applications in wastewater treatment, highlighting their efficiency in nutrient removal, heavy metal sequestration, and overall water quality enhancement. Although microalgae demonstrate remarkable potential for wastewater treatment, there is a critical gap in research concerning the utilization of biomass produced during the treatment process, including large-scale biomass harvesting methods, economic viability assessments, and the exploration of innovative downstream applications. By shedding light on these deficiencies, the aim of this review is to encourage further research and development to maximize the potential of microalgae in removing wastewater pollution and the application of biomass derived from the treatment. In conclusion, this review not only underscores the overall efficiency of microalgae in wastewater bioremediation but also emphasizes the necessity of a more comprehensive approach that considers the full lifecycle of microalgae, from wastewater treatment to innovative applications of biomass, addressing both environmental and economic concerns.

1. Introduction

Chemical water pollution has emerged as a significant concern and priority for society, public authorities, and especially the industrial sector. The sources of this pollution vary and include mining activities, industrial waste, urban wastewater (WW), sewage, pesticides and chemical fertilizers, energy usage, radioactive waste, and urban development [1]. Activities across the domestic, agricultural, and industrial sectors generate effluents containing harmful contaminants that expose human health and the environment to risks. Since these effluents are typically released into water bodies, it is crucial to continually protect water resources. Regulations governing the discharge of liquid industrial effluents are becoming increasingly stringent, particularly in developed countries, mandating that all wastewater should be treated before being discharged in nature [2]. The European Union Urban Wastewater Treatment Directive has been in effect for over 30 years, and since its adoption in 1991, there have been considerable improvements in the quality of European water bodies. European Union (EU) member states have established collection systems and wastewater treatment (WWT) facilities with the support of EU funding (https://environment.ec.europa.eu/topics/water/urban-wastewater_en; accessed on 15 July 2024). Currently, WW undergoes two main steps of treatment, namely primary and secondary treatment. The first is employed to remove large-size residues that could be present; the second one is mainly composed of aeration and settling tanks, where activated sludges are responsible for the removal of most of the pollutants. However, there are still issues with pollutants that are not covered by the current regulations. To address the latter, the Commission has proposed an update to the Directive [3]. Despite the progress made, traditional wastewater treatment methods are insufficient to completely remove many modern pollutants. Moreover, existing rules have not addressed pollution from smaller cities resulting from stormwater overflow. Paying attention to these challenges will be essential in order to achieve a pollution-free environment by 2050. More specifically, even though emerging pollutants (EPs) are frequently found in water bodies and are known to have dangerous effects on the environment, current legislation and treatment systems have not been able to deal with their proper removal from wastewater. Consequently, additional legislation and treatments to eliminate emerging contaminants before they enter the environment are urgently needed [4]. Microalgae are recognized as pollutant scavengers that are able to bioremediate a wide panel of chemicals released by several sectors, such as industrial, agricultural, and domestic. In addition to the common inorganic and organic compounds found in WW, such as heavy metals, xenobiotics, nitrates, phosphates, and carbon compounds, microalgal cells have the ability to uptake and decompose more persistent pollutants, such as antibiotics, polychlorinated biphenyls (PCBs), and hydrocarbons, which can be highly toxic to humans [5]. For instance, Zhou et al. [6] demonstrated that C. pyrenoidosa was capable of removing not only nitrogen and phosphorus from domestic WW, but also various heavy metals, such as mercury and silver (above 50%), as well as pharmaceuticals such as clarithromycin (around 80%). In addition, a microalgae-cyanobacteria consortium, namely Chlorella vulgaris, Scenedesmus quadricauda, and Arthrospira platensis, tested by Abdel-Razek et al. [7], was able to successfully remove malathion (up to 99%), a toxic pesticide, from urban WW. There are several papers in the literature demonstrating the efficiency of microalgae in removing excess of nutrients from water matrices; however, little is known about their ability to bioremediate emerging pollutants, either in pilot-scale systems or in real case scenarios [8]. In the context of a circular economy, this review aims to provide an updated overview of the release of major emergent pollutants, their already established treatments, which is the role of microalgae in these processes, and finally, to discuss what is missing to further implement microalgae-based treatment technologies.

2. Wastewater Composition and Conventional Treatment

The production of waste resulting from human activities is an inevitable fact of life, and a significant part of this waste consists of WW. The amount and quality of WW differs depending on several factors. In the case of households, the properties of their WW are influenced by residents’ lifestyle, customs, socioeconomic status, and the societal environment in which they live [9]. By contrast, the WW composition of industries is affected by the processes used. WW is a multifaceted blend of various substances, and its composition can vary depending on its origin, treatment methods, and regional characteristics. A general list of the common types of WWs and the main pollutants present in each of them is reported (Table 1).
As can be seen from the diversity of compounds and the wide range of concentrations listed in Table 1, WW is a significant contributor to water pollution when it is not appropriately collected or treated in compliance with EU regulations. It contains elements like organic matter, nitrogen, and phosphorous compounds, which, when effectively treated, are removed to prevent eutrophication. Additionally, WW can become contaminated with harmful chemicals, bacteria, and viruses. If left untreated and released into the environment, these contaminants can negatively impact our health and harm our rivers, lakes, and coastal waters. Moreover, emerging pollutants in WW are a diverse group of contaminants that are gaining increasing attention due to their potential harm to both human health and aquatic ecosystems. These pollutants are characterized by their recent identification, increased detection in environmental media, and growing understanding of their potential impact. EPs often include substances that have not been widely recognized or studied in the past (see Chapter 3 for a more complete description). Advances in analytical techniques and increased awareness have led to the identification of new compounds in the environment. Additionally, they exhibit persistence in the environment, resisting degradation over time, showing the potential to bioaccumulate in living organisms, and posing risks to higher trophic levels in ecosystems.

Wastewater Treatment

Primary and secondary WWT are two essential stages in the process of cleaning and purifying domestic and industrial WW. Primary treatment is the first step, involving physical processes, such as sand filters and screening, to remove large debris, solids, and some organic matter. It effectively reduces the volume of pollutants in water but does not completely eliminate them, and it is important to note that primary treatment alone may not be sufficient to meet stringent water quality standards, especially in terms of removing dissolved pollutants, nutrients, and pathogens. Briefly, WW first enters the treatment facility and passes through screens or bars that catch large objects such as sticks, rags, plastics, and other debris [75]. The WW then enters a primary clarifier, namely a sedimentation tank or settling tank. Here, the flow velocity of the water is reduced significantly, allowing suspended solids and organic matter to settle to the bottom of the tank due to gravity. This forms a layer of sludge, while relatively clear water rises to the surface [76]. Any floating material, grease, or oil that accumulates at the surface of the sedimentation tank is skimmed off using mechanical skimmers or scrapers for further treatment or disposal. After that, the settled sludge at the bottom of the sedimentation tank is pumped out and sent to a sludge treatment process for further processing, such as dewatering and digestion. After primary treatment, WW undergoes secondary treatment processes in which biological and chemical methods are employed to further remove dissolved and suspended organic matter, as well as nutrients like nitrogen and phosphorus [77]. This may include the activated sludge process, which is a widely used method in which the primary treated WW is aerated and mixed with activated sludge, which is a suspension of microorganisms (bacteria, protozoa, and sometimes fungi) able to consume and break down organic pollutants in the WW [78]. Depending on the quality of the effluent required and the specific regulations governing discharge, after the primary and secondary treatment, WW might undergo tertiary treatment, such as filtration, disinfection (using chlorine, ultraviolet light, or ozone), or advanced oxidation to remove remaining contaminants and pathogens [79]. Certain organic contaminants may not respond well to chemical or conventional activated sludge methods of treatment. For instance, traditional activated sludge treatment effectiveness, studied in the French AMPERES research, showed an efficiency below 30% for 24 chemicals out of 97 [80]. As a result, water companies are adopting specialized treatment procedures to lower the concentration of emerging pollutants in wastewater treatment plant (WWTP) effluent water. The development of either additional or substitute advanced treatment processes, such as bioremediation through microalgae, could be a solution to further improve water quality, thus helping protect ecosystems and public health. Moreover, WWT is one of the biggest consumers of energy in the public sector; thus, the development of new and more sustainable techniques is mandatory.

3. Emergent Pollutants

“Emerging pollutants” is a broad term used to describe substances and groups of substances that have become the focus of scientific or political concern at specific times due to their environmental relevance. The definition by Farré et al. in 2008 from water analytics is as follows: “emerging pollutants are defined as compounds that are not currently covered by existing water quality regulations, have not been studied before, and are thought to be potential threats to environmental ecosystems and human health and safety’ [81].
EPs are gaining attention due to their enduring nature, ability to accumulate in organisms, and resistance to typical WWT techniques. Even in small amounts, these contaminants can interfere with the organism’s endocrine systems, damage aquatic life, and potentially infiltrate the food chain. The cumulative harmful effects on aquatic organisms and the environment are not yet fully comprehended, underscoring the importance of monitoring and addressing their existence and removal. In recent years, the presence of EPs like pharmaceuticals, endocrine disruptors, insecticides, and personal care products, has been detected in surface water, WW, and groundwater sources globally [82,83]. To mitigate these detrimental effects, various methods of EPs degradation and/or removal have been investigated. Numerous past and ongoing studies have concentrated on eliminating these contaminants using a range of treatment techniques, encompassing physical, chemical, and biological approaches. Innovative treatment approaches, including advanced oxidation processes and the utilization of natural biofilters like microalgae, are being investigated to diminish the presence of these contaminants in WW. The current European legislation relevant to emerging pollutants primarily falls under the framework of the European Union’s water and chemical regulations. Key directives and regulations that address these pollutants include
  • Water Framework Directive (1997/0067(COD); WFD): a cornerstone of EU water policy aimed at protecting and restoring water bodies by preventing and reducing pollution. Emerging pollutants are a concern under the WFD as they can contaminate water bodies and affect aquatic ecosystems [84,85].
  • Priority Substances Directive (2000/60/EC PSD): identifies an index of priority compounds that need to be surveilled and controlled in European waters. Some emerging pollutants, like pharmaceuticals and personal care products, may be included in this list [86]. However, as our understanding of environmental risks evolves, new substances of concern are identified and added to the list if they meet certain criteria regarding their persistence, bioaccumulation, toxicity, and potential for widespread environmental exposure. Once included in the list, these substances are subjected to monitoring, assessment, and control measures to mitigate their impacts on water quality and safeguard ecosystems and public health.
  • Pharmaceuticals in the Environment (EMEA/CHMP/SWP/4447/00): The European Medicines Agency (EMA) has issued guidelines on the environmental risk assessment of pharmaceuticals, ensuring that pharmaceutical companies consider the environmental impact of their products [87].
  • Registration, Evaluation, Authorization, and Restriction of Chemicals (REACH Regulation; 1999/45/EC) addresses the registration, evaluation, and authorization of chemicals. It plays a role in managing and controlling industrial chemicals, some of which may be considered EPs [88].
  • Biocidal Products Regulation (528/2012/EU; BPR): regulates the use of biocidal products, which include chemicals used for disinfection and pest control. Some of these products may be considered EPs when they find their way into the environment [89].
  • Wastewater Treatment and Discharge Regulations (91/271/EEC): European nations have specific regulations for WWT and discharge. These regulations often include standards for the removal of EPs, particularly in urban areas [3].
  • European Pharmacopoeia: This reference work contains quality standards for medicines in Europe and includes guidelines on the environmental risk assessment of pharmaceuticals [90].
Although these existing regulations provide a framework for addressing EPs, there are still some challenges that need to be addressed. On the one hand, monitoring and risk assessment are the most valuable ways to set up new technologies and fill regulatory gaps. Nevertheless, policymakers must continually update and expand regulations to keep pace with the evolving scientific knowledge.
It is important to point out that the presence and impact of these EPs can vary widely depending on their specific chemical properties and how they are used and disposed. Additionally, the list of EPs continues to evolve as new compounds are identified and studied, making ongoing research and regulatory efforts essential to effectively address this environmental and public health challenge. The main categories of EPs are reported in Table S1 (Supplementary Material); however, the list is expanding daily, posing a multifaceted challenge for European regulators and researchers. Current European legislation provides a foundation for addressing these contaminants; however, ongoing efforts are required to enhance monitoring, risk assessment, and regulation to ensure the protection of the environment and human health in the face of a continuously evolving array of emerging pollutants [91,92].

4. Microalgae as a Promising Solution

Reducing climate change, using natural resources sustainably, and lowering environmental pollution are today’s major global challenges. Global food, water, and energy demands are predicted to increase by 60%, 80%, and 50%, respectively, between 2000 and 2050 [93,94]. One logical approach to reducing water consumption and demand could be to integrate WWT with algal cultivation, as both industries operate on comparable scales and utilize similar production facilities; thus, the application of microalgae for WWT could be a valuable solution among the others [95,96]. WWT systems utilizing microalgae offer inherent disinfection capabilities and surpass traditional WWT approaches in mitigating nutrient pollution. Unlike conventional methods with drawbacks like elevated operational expenses and inevitable secondary pollution from chemical procedures, microalgae stand out as highly effective decontaminating agents [97]. Their notable surface-to-volume ratios result in impressive biosorption capacities, allowing them to eliminate harmful substances. Additionally, many microalgae species exhibit versatility by transitioning between photoautotrophic, mixotrophic, and heterotrophic growth modes [98]. Compared to exclusively heterotrophic microorganisms, the main benefit of utilizing microalgae is that their growth is not restricted by decreasing pollution concentrations. The growth rate of microalgae may vary depending on different factors, such as species, nitrogen and phosphorus concentrations, and light intensity [99]; however, their adaptability represents an additional resource for this application.

4.1. How Do Microalgae Work?

The removal of contaminants by microalgae can occur in different ways, such as bioconversion, bioadsorption, and bioaccumulation [100].

4.1.1. Bioconversion

One highly effective method for removing pollutants from wastewater is bioconversion, wherein composite compounds are broken down into simple, harmless chemical building blocks that can be used as carbon sources. Unlike biosorption and bioaccumulation, in which microorganisms act as biological filters to separate and concentrate pollutants from water, biodegradation involves the decomposition of target pollutants. This can occur through biotransformation, which is a sequence of enzymatic events that result in different metabolic intermediates, or through full mineralization of the parent molecules into CO2 and H2O [101,102]. The fundamental mechanisms of biodegradation fall into two groups: (i) metabolic degradation, in which pollutants act as electron donors/acceptors and carbon sources for microalgae and (ii) cometabolism, where pollutants serve as both electron donors and carbon sources [103]. Biodegradation mediated by microalgae can occur in the extracellular or intracellular environment or through both. Enzymes present in microalgae, or released into the medium by them, such as peroxidases, azo-reductase, and laccases reported by several authors [101,102,104,105], are able to break down these complex molecules into simpler molecules to be used as metabolites by different mechanisms. Extracellular degradation involves the excretion of enzymes by microalgae, which break down pollutants outside the cell walls, enabling the mineralization of dissolved pollutants and functioning like an external digestive system. Additionally, this process may lead to an increase in the bioavailability of pollutants in the environment, hence facilitating microalgae following bioaccumulation. Three stages of intricate enzymatic reactions are involved in the microalgae-based biodegradation of organic contaminants. Stage I employs cytochrome P450 enzymes, including hydroxylase, carboxylase, decarboxylase, and monooxygenase, which enhance the hydrophilicity of the pollutant by adding or revealing a hydroxyl group through oxidation-reduction reactions or hydrolysis [101,106]. In stage II, enzymes such as glutathione-S-transferases and glucosyltransferases facilitate the conjugation of glutathione with various compounds possessing electrophilic centers to protect the cell from oxidative damage [107]. The third stage of detoxification involves a range of enzymes, including oxidoreductases, such as glutamyl-tRNA reductase, carboxylases, mono(di)oxygenases, laccases, transferases, hydrolases, pyrophosphatases, and dehydratases, which convert compounds into intermediates that are either less harmful or non-toxic [104]. In contrast, cometabolism involves the use of pollutants as both electron donors and carbon sources. These organic substrates act as electron donors, aiding in the co-metabolization of EPs and biomass [108]. To enhance microalgae-mediated biodegradation of persistent pollutants, some studies have suggested adding nutrient substances or organic substrates to create a co-metabolic system [109]. Vo et al. [109] demonstrated that adding glucose to Chlorella sp. cultures increased the removal efficiency of all EPs tested, namely, tetracycline, sulfamethoxazole, and bisphenol A, above 80%. Although research indicates that the highest concentrations of detoxifying enzymes and the best removal effectiveness come from employing sugar-carbon sources, adopting some of them may decrease the removal efficiency of EPs, most likely as a result of catabolite suppression [108]. Therefore, it is essential to evaluate different carbon sources to identify the most suitable ones for effective pollutant biodegradation in wastewater.

4.1.2. Bioadsorption

Bioadsorption involves the adsorption of compounds (sorbates) by microalgae onto the cell membrane (solid-phase sorbent) [110]. While bioconversion can only be carried out by living cells, bioadsorption can be carried out by either living or dead cells [111]. Biosorption involves physical, chemical, and metabolic-independent processes facilitated by mechanisms such as precipitation, ion exchange, surface complexation, and electrostatic interactions [112]. Microalgae contain functional groups on their membranes that make them negatively charged, attracting metal ions (usually dissolved in the form of cations) via electrostatic forces. The large surface area of small-sized cells in large quantities in water aids the removal process [113,114]. Furthermore, microalgae contribute to the organic matter suspended in water, which is capable of adsorbing other organic compounds, such as dyes or other organic pollutants. The high affinity of the biosorbent for the target sorbate drives the attraction of the sorbate molecules [110,111]. The process continues until equilibrium is reached between the sorbate adsorbed by the biosorbent and its remaining concentration in the liquid. Moreover, the porosity and roughness of the microalgae surface affect heavy metal adsorption [115]. Trace elements like manganese, molybdenum, cobalt, copper, zinc, iron, and boron are essential for enzymatic processes and cell metabolism but can be toxic at high concentrations. In contrast, heavy metals such as chromium, cadmium, mercury, lead, and arsenic are generally toxic to microalgae [116]. Flocculation can be promoted by active binding sites on the cell surface, forming complexes with specific pollutants and reducing total dissolved and suspended solids [4]. Mota et al. [117] discovered that polymeric material released by Cyanothece sp. can sequester heavy metals from contaminated water due to carboxyl and hydroxyl functional groups rather than ion exchange.

4.1.3. Bioaccumulation

Microalgae can accumulate various pollutants along with nutrients and microelements [118]. Differently from biosorption, bioaccumulation requires energy since it is an active metabolic process, resulting in a relatively slow system [119]. This process is crucial for removing inorganic and organic pollutants (such as sulfates, nitrates, phosphates, heavy metals, and pesticides) as these substances are transferred into the cells [110]. Additionally, changes in cell membrane permeability due to pollutants or environmental stress can result in passive diffusion mediated by membrane depolarization or hyperpolarization [120]. Although bioaccumulation and biosorption are fundamentally different, quantifying the pollutants processed by each mechanism is challenging because the two mechanisms are dynamically interrelated. Previous studies have reported the bioaccumulation of sulfamethoxazole, trimethoprim, florfenicol, and carbamazepine, where these pollutants enter microalgal cells through passive diffusion [121]. For instance, the cyanobacterium Anabaena CPB4337 showed altered sensitivity to herbicides when exposed to perfluorinated alkyl acid compounds like perfluorooctane sulfonate and perfluorooctanoic acid, with some herbicides becoming more toxic and others less toxic [122]. Moreover, Xiong et al. [102] demonstrated that the bioaccumulation of levofloxacin by Chlorella vulgaris significantly increased from 34 to 101 μg/g with the addition of 1% (w/v) NaCl.
In addition, microalgae can help reduce greenhouse gas (GHG) emissions by aiding in the sequestration of carbon dioxide (CO2) from the atmosphere or from industrial flue gases. Moreover, wastewater’s aquatic environment provides an ideal environment for microalgae to grow. The synergistic relationship between microalgae and bacteria provides additional opportunities and benefits in WWT [123], enhancing the overall efficiency and effectiveness of the WWT processes. Microalgae have the ability to assimilate nitrogen and phosphorus compounds from WW through photosynthesis [124]. Bacteria can further transform nitrogen compounds, such as ammonia and nitrate, into nitrogen gas through biological processes like nitrification and denitrification [125]. This combined action of microalgae and bacteria promotes the efficient removal of nutrients from WW, reducing the risk of eutrophication in receiving water bodies. Microalgae produce oxygen as a byproduct of photosynthesis, which increases the dissolved oxygen levels in WW. This oxygenation is beneficial for aerobic bacteria, which require oxygen to effectively metabolize and degrade organic pollutants [126,127]. Oxygen aeration represents more than 50% of the energetic needs of a WWTP; thus, from an economical point of view, the synergistic use of microalgae and bacteria can reduce the overall cost of the process [128]. The efficiency of the algal-bioremediation processes discussed earlier is influenced by a range of physicochemical factors, including pH, redox potential, temperature, duration and strength of light exposure, hydraulic retention time, size of adsorbents, and concentration of environmental pollutants [129].

4.1.4. Temperature, pH, and Hydraulic Retention Time

Industrially generated WW effluents often exhibit elevated temperatures, posing the risk of thermal pollution in aquatic ecosystems [130]. Although different microalgae species have specific temperature requirements, they can generally thrive within a broad temperature range. The optimal temperature for commonly cultivated microalgae typically falls between 15 and 28 °C [131]. Once this optimal temperature is surpassed, there is a noticeable decline in biomass productivity. Temperature fluctuations pose a significant challenge in the cultivation of microalgae. Hence, microalgae species capable of thriving in high-temperature WW environments (around 30–40 °C) are crucial for effectively utilizing these organisms in the bioremediation of emerging pollutants [132].
pH serves as a critical factor influencing the effectiveness of algal-bioremediation mechanisms, playing a role in altering the ionization states of various functional groups present on the surface of microalgae [133]. Any deviation from the optimal pH level for a biological process can reduce the reaction rate. This occurs because the charge of the cell membrane of microalgae is positive owing to lower pH levels, leading to decreased molecule adsorption. Conversely, when the pH surpasses the isoelectric point, the algal surface acquires a negative charge, resulting in enhanced absorption [134]. Specifically, pH levels exceeding 9 have a detrimental effect on algal growth, as they significantly reduce the capacity for carbon dioxide absorption and hinder the activity of RuBisCO, decreasing photosynthetic activity [135].
The hydraulic retention time (HRT) can influence certain mechanisms by which microalgae uptake pollutants. In certain instances, a shorter hydraulic retention time may result in partial or ineffective elimination of pollutants. The efficacy of pollutant removal depends on both the biomass of microalgae present and the hydraulic retention time since a very short HRT could lead to washout of the culture [136]. Removal rates tend to increase with higher concentrations of microalgae and longer hydraulic retention times up to a certain limit [137].

4.1.5. Particle Size and Adsorbent Dose

The permeability for absorption into the cell wall improves as the pollutant particle size decreases, and this interaction is affected by the pollutant’s toxicity. This effect is due to the increased surface area, which provides more binding sites. The functional groups engaged in the interaction, electrostatic capacity, and surface area are some of the factors that affect algal bioremediation by adsorption. Moreover, longer hydraulic retention durations between the contaminants and the adsorbent have been shown to boost absorption [138,139].

4.1.6. Light Exposure and Redox Potential

Photolysis and hydrolysis help reduce the persistence and toxicity of pollutants in the environment and are two key processes that break down pollutants in the environment. The first is the breakdown of pollutants due to exposure to sunlight, particularly to ultraviolet (UV) radiation. The latter causes the chemical bonds within the pollutant molecules to break, leading to their degradation into smaller molecules. The second mechanism consists of the chemical breakdown of pollutants by water. Water molecules react with the pollutant, leading to the cleavage of chemical bonds, resulting in the formation of new, often less toxic, compounds [140,141].
The efficiency of microalgae in bioremediation is influenced by a range of biological, nutrient, and environmental factors in addition to the abovementioned factors [142]. Biological factors include the specific algal species used, as different species have varying capacities for pollutant uptake and degradation [143]. The growth phase of the algae also impacts its bioremediation potential, with different stages of growth showing different levels of activity. Furthermore, interactions with other microorganisms such as bacteria and fungi can either enhance or inhibit algal performance [144]. Nutrient availability is another crucial factor; the composition and availability of essential nutrients like nitrogen, phosphorus, and micronutrients are vital for optimal algal growth and pollutant removal. Conversely, nutrient limitation can significantly hinder these processes [101]. Environmental factors such as salinity levels and the presence of inhibitors like toxic substances, can also affect algal growth and bioremediation efficiency, as high salinity or toxic inhibitors can suppress algal activity and pollutant uptake [145]. While axenic (pure) microalgae cultures can offer more controlled conditions and higher efficiency in pollutant removal, they present significant economic drawbacks. Maintaining axenic cultures is costly and labor-intensive, requiring sterile conditions and specialized equipment to prevent contamination [146]. This increases the overall cost of the bioremediation process, making it less economically viable for large-scale applications. Additionally, the need for continuous monitoring and the risk of culture collapse further adds to operational expenses, limiting the practicality of using axenic microalgae cultures in real-world scenarios. Understanding these factors is essential for optimizing microalgae-based bioremediation systems while balancing their efficiency and economic feasibility.

4.2. Microalgae-Based Wastewater Treatment

In recent times, there has been a growing concern regarding the presence of PAHs, PCBs, pesticides, pharmaceuticals, and heavy metals, among other pollutants in water. In Europe, the Water Framework Directive (Directive 2000/60/EC) does not mandate that WWTPs address these micropollutants. However, it does specify a list of substances that member states need to monitor. Additionally, the REACH regulation (2006) bolstered EU regulations by requiring a risk assessment of 30,000 chemical substances. The European Union IPPC (Directive 2008/1/CE) and subsequently the Industrial Emission Related Directive (Directive 2010/75/UE) have replaced the Water Framework Directive. These directives call for the application of the best available techniques (BAT), considering both technical and economic preventive measures, pollution control technologies, and efficient resource consumption. Given the bioremediation potential of microalgae, there is a specific opportunity to innovate and implement new technologies for WW bioremediation based on microalgae. Currently, several research groups are studying the use, mechanisms, and efficiencies of a wide variety of microalgae strains and consortia for WWT (Table 2).
As shown in Table 2, microalgae can effectively remove nutrients from wastewater. Di Cicco et al. demonstrated that Galdieria phlegrea, an extremophilic microalga, removed about 70% and 22% of ammonium and phosphates, respectively, from urban WW [147]. Daneshvar’s research team also studied the removal of nutrients from municipal wastewater using Tetraselmis suecica and Scenedesmus quadricauda. The results showed that S. quadricauda outperformed T. suecica, achieving removal efficiencies of 95.3% for nitrates and 89.8% for phosphates [150]. As nutrient removal with microalgae is an already established reality, some researchers have shifted their attention to the clean-up of EPs from WW. For instance, Zhou et al. [6] reported that some microalgae species, including C. reinhardtii and C. pyrenoidosa, were able to remove a wide variety of heavy metals, such as silver and mercury, and pharmaceuticals, such as clarithromycin, with removal efficiencies above 50% and above 80%, respectively, from domestic WW. Ajayan et al. also reported high removal rates of heavy metals, including lead, by Scenedesmus sp., cultivated in tannery WW. After 12 days of growth, Scenedesmus sp. removed between 75% and 98% of lead [149]. Similar removal efficacies for this metal were also reported by Abdel-Razek et al. for both urban and agricultural WW samples using a consortium of Chlorella vulgaris, Scenedesmus quadricauda, and Arthrospira platensis [7]. Moreover, this designed consortium of microalgae and cyanobacteria was able to successfully remove malathion (up to 99%), a toxic pesticide, from the same WW samples [7]. A similar consortium of Chlorella vulgaris and Arthrospira platensis was reported to be able to remove polyphenols from winery WW with removal yields above 50% [148]. Moreover, two species of the genus Chlorella, C. vulgaris and C. pyrenoidosa, have been documented by Premaratne et al. to have high decolorizing power for various types of dye: “Indigo” (89.3%), “Direct blue” (79%), “Remazol brilliant orange” (75.3%) and “Crystal violet” (72.5%). During this process, the COD of the WW was diminished by 70% [100,159]. Moreover, Saavedra et al. investigated the influence of organic matter or CO2 on heavy metal removal from synthetic WW using Chlorella vulgaris and Scenedesmus almeriensis [123]. Noteworthy is the fact that most of the results reported in Table 2 were obtained at a laboratory scale, indoors, with the use of artificial light (ranging from 45 to 100 μmol/m·s) and, most importantly, of low working volumes, with 10 L being the highest tested volume. In addition, given the small-scale experiments, no information on the hydraulic retention time, one of the most major parameters, is provided. In Table 2, only two research works are reported that have been carried out with larger volumes; Sayara et al. evaluated the role of the natural consortium of microalgae and cyanobacteria in scavenging ammonium and phosphorus (55% and 91%, respectively) from domestic WW [154], while, Serrà et al. demonstrated the ability of Arthrospira platensis to remove heavy metals from industrial WW. However, only the latter applied the concept of a more circular approach, as the results suggested that biomass could be used in the production of bioethanol [157]. For this reason, industrially relevant studies with larger volumes under real atmospheric conditions and with real WW are required before considering the large-scale application of microalgae in the treatment of WW. On top of that, most of the papers mentioned in Table 2 describe the rates of pollutant removal by the microalgae-based treatment; however, none of them focus on the contamination level of the biomass itself. It is important to keep in mind that using WWs as a culture medium may lead to differences in microalgae biomass, such as higher lipid or protein content. Moreover, it is worth evaluating the degree of contamination of the biomass and quantifying the pollutants that have been taken up/sequestered by the biomass from the medium.

Drawbacks

From an industrial and commercial point of view, microalgae are typically grown in artificial nutrient solutions, which adds a significant expense to the product. Nonetheless, this cost fluctuates depending on the specific species employed, and it can be mitigated by using waste materials as a source of nutrients. Chisti et al. [160] assessed the expenses associated with establishing Arthrospira platensis biomass production facilities, while Fernández et al. [161] conducted an in-depth analysis on a case study involving a 5-hectare facility utilizing open reactors, raceway, and thin-layer cascade systems. The results confirm that the production costs of microalgae biomass for these applications are 4.5 and 2.3 €/kg when employing the raceway and thin-layer cascade, respectively. To achieve cost reduction, it is essential to utilize WWs as a nutrient source, leading to biomass production costs of 3.6 and 1.4 €/kg for the raceway and thin-layer cascade, respectively. Further cost reduction necessitates a significant decrease in the manpower required for the process operation. By reducing up to 0.1 person/ha, the biomass production cost can be lowered to 2.6 and 0.8 €/kg for raceway and thin-layer cascade production systems, respectively. When considering the process as a WWT method, the treatment cost can be minimized to 1.1 and 1.2 €/m3 for raceway and thin-layer cascade, respectively. These costs are still higher than those associated with conventional WWT systems, which stand at 0.2 €/m3. However, if the WWT cost is included as an input for biomass production, the final biomass production cost can be reduced to minimum values of 2.1 and 0.6 €/kg using the raceway and thin-layer cascade, respectively. Thus, replacing synthetic media with industrial effluents emerges as a crucial alternative for cost reduction in microalgae production, simultaneously serving as a means to treat effluents, rather than relying on conventional physical, chemical, and biological methods [162]. WWs exhibit nitrogen and phosphorus concentrations up to three times higher than those found in natural water bodies [163,164], and microalgae rely on these nutrients for energy exchange and growth, reducing the overall eutrophication potential of WWs [165]. Consequently, these microorganisms are able to grow sufficiently, offering a high number of cells that can contribute to effluent bioremediation by removing pollutants from the water or even breaking down contaminants into metabolites that are less harmful than the parent compounds [166]. To address the global challenges of water scarcity and the non-renewability of phosphorus [167], the rational use of nutrients and water is vital. Valorizing biomass after WWT is crucial from a circular economy perspective. In this sustainable approach, the by-products of WWT, which are rich in organic matter, are not treated as mere waste but as valuable resources. The biomass obtained from WW can be harnessed to produce biogas, biofuels, or even biobased chemicals. Indeed, the most important aspect for governments and policymakers is the quality of water at the end of the process. However, depending on the abovementioned factors, biomass can find different applications that generate revenue, help mitigate the costs of the overall processes, and increase the circularity of WWT. By integrating these biomass valorization techniques into the circular economy model, the loop of resource usage can be closed, promoting a regenerative system where waste becomes a feedstock for new products. This not only minimizes the environmental impact but also contributes to energy generation and the development of a biobased economy, fostering a more sustainable and resilient future.

5. Biomass Utilization

In addition to their capacity for carbon capture, microalgae are a rich source of diverse molecules, with potential applications spanning from biofuel production [168,169] to industries such as cosmeceuticals and nutraceuticals. Given the recognized long-term drawbacks associated with synthetic compounds, there is an urgent need to explore new natural substances possessing beneficial properties [170], making microalgae a promising alternative. For instance, dried biomass can be repurposed as animal feed [171] or fertilizer [172], and the carbohydrates present in microalgae can be utilized for lactic acid production [173,174] or for bioplastic production [173,175]. Depending on the predominant microalgae strain, the dried wastewater-grown biomass can also be used as a feedstock for valuable compounds. For example, phycocyanin can be obtained from cyanobacteria [176], whereas other microalgae may be a source of high-value molecules like omega-3 [177] or carotenoids [178], which are often used as natural colorants in the food sector because of their remarkable color, antioxidant, and preservative properties [179]; however, the applicability of wastewater-grown microalgal biomass may be limited due to specific optimization process requirements that affect the productivity of such compounds, and strict industry regulations that prevent the use of biomass produced in WW. Therefore, it is crucial for microalgae biomass intended for such applications to be free of persistent pollutants like heavy metals, which could adversely affect animals, soil, or groundwater. The transition from lab- to industrial-scale processes often involves several challenges, engineering, chemistry, economics, and regulatory compliance, which can result in loss of productivity. Addressing these challenges requires careful planning, experimentation, and continuous optimization to ensure a smooth transition and to maintain or improve productivity on a larger scale.
The most promising application of this biomass appears to be in the energy market, where drying can be avoided [180]. A considerable number of studies have highlighted the essential role of WW in advancing the microalgae biofuel production industry [181,182,183,184]. Presently, microalgae production is expensive, leading to costs as high as 100 €/kg of biomass. For instance, a 30 m3 tubular photobioreactor plant incurred a production cost of 69 €/kg of dry weight over two years of continuous operation [184]. Moreover, the differences between these costs and the aforementioned costs are mainly due to the production system adopted. Closed and open bioreactors primarily differ in operational complexity, environmental control, and resource requirements. For instance, Oostlander et al. [185] carried out techno-economic analyses on the operational costs of producing microalgae in tubular-shaped reactors and airlifts, both under artificial light, in the Netherlands, determining a cost of 290 €/kg and 587 €/kg, respectively. The reported costs in the literature may vary widely because of the location and system of the production of microalgae. In summary, open bioreactors have lower initial and operating costs but may be less productive and more prone to environmental disruptions, while closed bioreactors, though more expensive, offer higher yields and better control over production conditions. Only through techno-economic projections is it possible to estimate the costs for large-scale production, but outcomes vary based on assumptions and key parameter values like lipid productivity.
In Table 2, different applications of the biomass obtained with diverse WWs as culture medium are shown. Several authors have studied the efficiency of microalgae in WWT; nevertheless, only a few of them have focused on the further utilization of the biomass obtained through these cultivations. Papadopoulos et al. demonstrated the ability of a cyanobacteria consortium to remove heavy metals from electrochemically pretreated brewery WW and to obtain carbohydrate-enriched biomass for bioethanol production [153]. Lima and colleagues confirmed that the lipid content of biomass can vary depending on cultivation conditions. They evaluated the total nitrogen and total phosphorous removal from municipal WW with different indigenous strains from Sicily, resulting in biomass fitting for biofuel production [156].
Following biomass harvesting and water removal, the dry weight concentration typically ranges from 15% to 25% [186]. For example, it is possible to extract lipids by procedures applied to the wet biomass, converting it into energy [187], such as anaerobic digestion or hydrothermal liquefaction (HTL), and then converting them via transesterification [188]. Recent screenings have identified strains that grow on WW and accumulate lipids simultaneously (up to 23.7 mg/L/day) [189]. Anaerobic digestion efficiently converts microalgae biomass into biogas but currently lacks economic viability. Competing with the globally low price of natural gas poses a challenge for biogas obtained by anaerobic digestion. Furthermore, the expense associated with anaerobic digestion exhibits considerable variability across different feedstocks, primarily because of economies of scale [190]. HTL is a thermochemical process, and its main advantage is the direct use of wet biomass as feedstock, reducing the overall energy demand, eliminating the drying stage of the biomass [191], and transforming wet biomass into bio-crude, gas, residual solids, and an aqueous phase rich in nutrients. Although several papers have recently been published in the literature, there are still gaps in the process for a large-scale application, such as corrosion in reactor tubes, salt deposition, product stability, heat recovery, and emulsion [191].
In order to improve the sustainability of the process and decrease the overall production costs, recycling of cultivation media has been explored [192,193,194]. Despite these efforts, the petroleum diesel cost (0.6 €/L) still represents an unreachable point for microalgae-based biodiesel, mainly due to the estimated production cost (2.5 €/L) [195]. Microalgal biomass obtained from cultivation on WW may not always meet safety regulations due to its chemical and biological composition, fouling by pathogenic organisms, or toxic pollutants. In such cases, converting low-grade biomass into biochar through pyrolysis emerges as a valuable alternative. Depending on the biochar composition, it can be utilized as a soil amendment [196], minimizing the risk of leaching toxic materials like heavy metals, as the pyrolysis process captures these metals in the solid matrix [197].

6. Final Considerations

Microalgae biomass possesses numerous potential uses, with the most promising large-scale application being adopted as biofuels [198]. Additionally, they have already established roles in high-value markets such as human dietary supplements (nutraceuticals) and animal feed [199]. However, achieving economic, energetic, and, above all, environmental sustainability in microalgae production requires significant advancements [180]. One promising opportunity for microalgae is their utilization in WWT. Wastewaters are rich in nitrogen and phosphorus, which are essential nutrients for microalgal growth [163,200]. Thus, microalgae can help remediate effluents by converting contaminants into nutrients and less toxic substances [166]. This approach, known as a microalgae-based biorefinery coupled with biochemical effluent treatment, is gaining interest in the scientific community. Commercially, microalgae are typically grown in synthetic media, which can be expensive. However, the cost varies depending on the scale and the specific species used, and it can be reduced by using effluents from industrial processes. Several studies have demonstrated that the culture medium can account for a significant portion of the total production costs [160,201]. Moreover, the work from Feng et al. [202] demonstrated that growing Chlorella vulgaris in artificial effluent can reduce the cost of 1 ton of biomass by up to 3.5 times (from 750 € to 215 €). Substituting synthetic media with industrial effluents not only reduces costs, but also provides a means of treating these effluents, which is more environmentally friendly than traditional methods. This approach not only offers a cost-effective means of cultivation but also a new potential market segment. Microalgae are able to efficiently uptake a wide range of chemicals from water [203], regardless of their various nutritional modes (phototrophy, heterotrophy, and mixotrophy), conferring these microorganisms with high versatility and potential. Among the strategies for large-scale microalgal biomass production, combining WWT with algal farming makes sense owing to the similar scale and production facilities shared by both industries. An additional benefit of this approach is the improvement of local industries and the reduction in the environmental impact related to nutrient manufacturing, transportation, and changes in land use. It is crucial to conduct economic feasibility assessments for WWT systems based on microalgae and compare them to traditional methods, given the limited number of existing studies on pilot or industrial-scale production. Meanwhile, the absence of fundamental design and operational guidelines for microalgae-based WWT should serve as a driving force for researchers to intensify their efforts. Their aim should be to enhance the adaptability and robustness of microalgal strains in addressing diverse types of WW challenges to provide essential guidance and recommendations [165]. Moreover, improving the Technology Readiness Level (TRL) 3 to TRL 9 in a microalgae-based WWT is crucial for transitioning from laboratory research to full-scale commercial application. At TRL 3, the technology is still in the experimental proof-of-concept stage, where fundamental principles are being validated in controlled environments. Advancing through TRLs involves progressively refining the technology, optimizing processes, and scaling up systems to address real-world challenges, such as nutrient removal efficiency, cost-effectiveness, and environmental impact [204]. This progress is vital for meeting environmental regulations, reducing treatment costs, and contributing toward achieving circular economy objectives. The continuous development and discovery of new technologies in this field extimates the global microalgae market, reaching 1.143 USD billion by 2024, growing at a compound annual rate of 7.4% [205].

Supplementary Materials

The following supporting information can be downloaded at https://www.mdpi.com/article/10.3390/w16192710/s1, Table S1. Examples of EPs divided by major groups.

Author Contributions

Conceptualization, L.B. and D.L.; writing—original draft preparation, D.L., F.P. and B.S.; writing—review and editing, L.B. and J.V.; supervision, L.B.; project administration, L.B.; funding acquisition, L.B. and J.V. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the Portuguese Foundation for Science and Technology through projects UIDB/04326/2020 (DOI:10.54499/UIDB/04326/2020), UIDP/04326/2020 (DOI:10.54499/UIDP/04326/2020), LA/P/0101/2020, (DOI:10.54499/LA/P/0101/2020), and doctoral fellowship 2023.04611.BDANA. Additionally, funding was provided by the European Union through the RHE-MEDiation project (HORIZON-MISS-2022-OCEAN-01-03-101113045).

Acknowledgments

This work was developed within the scope of the Project “Blue Bioeconomy Innovation Pact”, co-financed by the Recovery and Resilience Plan (RRP) and NextGeneration EU through the Incentive System “Agendas for Business Innovation”. We would like to thank Biorender.com and Flaticon.com for providing the figures.

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. Madhav, S.; Ahamad, A.; Singh, A.K.; Kushawaha, J.; Chauhan, J.S.; Sharma, S.; Singh, P. Water Pollutants: Sources and Impact on the Environment and Human Health. In Sensors in Water Pollutants Monitoring: Role of Material; Springer: Berlin/Heidelberg, Germany, 2020; pp. 43–62. [Google Scholar]
  2. Johnstone, D.W.M.; Ilg, S.S.N. Effluent Discharge Standards. In Handbook of Water and Wastewater Microbiology; Elsevier: Amsterdam, The Netherlands, 2003; Volume 299. [Google Scholar]
  3. Bird, P. The Urban Waste Water Treatment Directive. Inst. Water Off. J. 1992, 28, 14–15. [Google Scholar]
  4. Al-Tohamy, R.; Ali, S.S.; Li, F.; Okasha, K.M.; Mahmoud, Y.A.-G.; Elsamahy, T.; Jiao, H.; Fu, Y.; Sun, J. A Critical Review on the Treatment of Dye-Containing Wastewater: Ecotoxicological and Health Concerns of Textile Dyes and Possible Remediation Approaches for Environmental Safety. Ecotoxicol. Environ. Saf. 2022, 231, 113160. [Google Scholar] [CrossRef]
  5. Mondal, M.; Halder, G.; Oinam, G.; Indrama, T.; Tiwari, O.N. Bioremediation of Organic and Inorganic Pollutants Using Microalgae. In New and Future Developments in Microbial Biotechnology and Bioengineering; Elsevier: Amsterdam, The Netherlands, 2019; pp. 223–235. [Google Scholar]
  6. Zhou, G.-J.; Ying, G.-G.; Liu, S.; Zhou, L.-J.; Chen, Z.-F.; Peng, F.-Q. Simultaneous Removal of Inorganic and Organic Compounds in Wastewater by Freshwater Green Microalgae. Environ. Sci. Process. Impacts 2014, 16, 2018–2027. [Google Scholar] [CrossRef] [PubMed]
  7. Abdel-Razek, M.A.; Abozeid, A.M.; Eltholth, M.M.; Abouelenien, F.A.; El-Midany, S.A.; Moustafa, N.Y.; Mohamed, R.A. Bioremediation of a Pesticide and Selected Heavy Metals in Wastewater from Various Sources Using a Consortium of Microalgae and Cyanobacteria. Slov. Vet. Res. 2019, 56, 61–73. [Google Scholar] [CrossRef]
  8. Hena, S.; Gutierrez, L.; Croué, J.-P. Removal of Pharmaceutical and Personal Care Products (PPCPs) from Wastewater Using Microalgae: A Review. J. Hazard. Mater. 2021, 403, 124041. [Google Scholar] [CrossRef]
  9. Henze, M.; Comeau, Y. Wastewater Characterization. In Biological Wastewater Treatment: Principles, Modelling and Design; Iwa Pub: London, UK, 2008; pp. 33–52. [Google Scholar]
  10. Hussain, I.; Raschid, L.; Hanjra, M.A.; Marikar, F.; Van Der Hoek, W. Wastewater Use in Agriculture: Review of Impacts and Methodological Issues in Valuing Impacts; International Water Management Institute: Sri Lanka, Colombo, 2002. [Google Scholar]
  11. Gupta, P.L.; Lee, S.-M.; Choi, H.-J. Integration of Microalgal Cultivation System for Wastewater Remediation and Sustainable Biomass Production. World J. Microbiol. Biotechnol. 2016, 32, 139. [Google Scholar] [CrossRef] [PubMed]
  12. Berlin, M.; Kumar, G.S.; Nambi, I.M. Numerical Modelling on Transport of Nitrogen from Wastewater and Fertilizer Applied on Paddy Fields. Ecol. Modell. 2014, 278, 85–99. [Google Scholar] [CrossRef]
  13. Kantawanichkul, S.; Somprasert, S. Using a Compact Combined Constructed Wetland System to Treat Agricultural Wastewater with High Nitrogen. Water Sci. Technol. 2005, 51, 47–53. [Google Scholar] [CrossRef]
  14. Guo, Y.; Sanjaya, E.H.; Wang, T.; Rong, C.; Luo, Z.; Xue, Y.; Chen, H.; Li, Y.-Y. The Phosphorus Harvest from Low-Temperature Mainstream Wastewater through Iron Phosphate Crystallization in a Pilot-Scale Partial Nitritation/Anammox Reactor. Sci. Total Environ. 2023, 862, 160750. [Google Scholar] [CrossRef]
  15. Köck-Schulmeyer, M.; Villagrasa, M.; de Alda, M.L.; Céspedes-Sánchez, R.; Ventura, F.; Barceló, D. Occurrence and Behavior of Pesticides in Wastewater Treatment Plants and Their Environmental Impact. Sci. Total Environ. 2013, 458, 466–476. [Google Scholar] [CrossRef]
  16. Westlund, P.; Yargeau, V. Investigation of the Presence and Endocrine Activities of Pesticides Found in Wastewater Effluent Using Yeast-Based Bioassays. Sci. Total Environ. 2017, 607, 744–751. [Google Scholar] [CrossRef] [PubMed]
  17. de Souza, R.M.; Seibert, D.; Quesada, H.B.; de Jesus Bassetti, F.; Fagundes-Klen, M.R.; Bergamasco, R. Occurrence, Impacts and General Aspects of Pesticides in Surface Water: A Review. Process Saf. Environ. Prot. 2020, 135, 22–37. [Google Scholar] [CrossRef]
  18. Gavala, H.N.; Skiadas, I.V.; Bozinis, N.A.; Lyberatos, G. Anaerobic Codigestion of Agricultural Industries’ Wastewaters. Water Sci. Technol. 1996, 34, 67–75. [Google Scholar] [CrossRef]
  19. Wei, Y.-S.; Yu, D.-W.; Cao, L. Anaerobic Membrane Bioreactors for Treating Agricultural and Food Processing Wastewater at High Strength. Huan Jing ke Xue = Huanjing Kexue 2014, 35, 1613–1622. [Google Scholar] [PubMed]
  20. Iliopoulou, A.; Zkeri, E.; Panara, A.; Dasenaki, M.; Fountoulakis, M.S.; Thomaidis, N.S.; Stasinakis, A.S. Treatment of Different Dairy Wastewater with Chlorella Sorokiniana: Removal of Pollutants and Biomass Characterization. J. Chem. Technol. Biotechnol. 2022, 97, 3193–3201. [Google Scholar] [CrossRef]
  21. Stasinakis, A.S.; Charalambous, P.; Vyrides, I. Dairy Wastewater Management in EU: Produced Amounts, Existing Legislation, Applied Treatment Processes and Future Challenges. J. Environ. Manag. 2022, 303, 114152. [Google Scholar] [CrossRef]
  22. Queiroz, R. de C.S. de; Andrade, R.S.; Dantas, I.R.; Ribeiro, V. de S.; Neto, L.B.R.; Almeida Neto, J.A. de Use of Native Aquatic Macrophytes in the Reduction of Organic Matter from Dairy Effluents. Int. J. Phytoremed. 2017, 19, 781–788. [Google Scholar] [CrossRef]
  23. Guillen-Jimenez, E.; Alvarez-Mateos, P.; Romero-Guzman, F.; Pereda-Marin, J. Bio-Mineralization of Organic Matter in Dairy Wastewater, as Affected by PH. The Evolution of Ammonium and Phosphates. Water Res. 2000, 34, 1215–1224. [Google Scholar] [CrossRef]
  24. Ashekuzzaman, S.M.; Forrestal, P.; Richards, K.; Fenton, O. Dairy Industry Derived Wastewater Treatment Sludge: Generation, Type and Characterization of Nutrients and Metals for Agricultural Reuse. J. Clean. Prod. 2019, 230, 1266–1275. [Google Scholar] [CrossRef]
  25. Huang, M.; Li, Y.; Gu, G. Chemical Composition of Organic Matters in Domestic Wastewater. Desalination 2010, 262, 36–42. [Google Scholar] [CrossRef]
  26. Selvarajan, R.; Sibanda, T.; Pandian, J.; Mearns, K. Taxonomic and Functional Distribution of Bacterial Communities in Domestic and Hospital Wastewater System: Implications for Public and Environmental Health. Antibiotics 2021, 10, 1059. [Google Scholar] [CrossRef] [PubMed]
  27. Ulrich, H.; Klaus, D.; Irmgard, F.; Annette, H.; Juan, L.-P.; Regine, S. Microbiological Investigations for Sanitary Assessment of Wastewater Treated in Constructed Wetlands. Water Res. 2005, 39, 4849–4858. [Google Scholar] [CrossRef] [PubMed]
  28. Subedi, B.; Balakrishna, K.; Joshua, D.I.; Kannan, K. Mass Loading and Removal of Pharmaceuticals and Personal Care Products Including Psychoactives, Antihypertensives, and Antibiotics in Two Sewage Treatment Plants in Southern India. Chemosphere 2017, 167, 429–437. [Google Scholar] [CrossRef] [PubMed]
  29. Mahendra, B.G.; Patil, S. Anaerobic Digestion of Domestic Wastewater. Int. J. Res. Eng. Technol. 2013, 2, 283–287. [Google Scholar] [CrossRef]
  30. Aderibigbe, D.O.; Giwa, A.-R.A.; Bello, I.A. Characterization and Treatment of Wastewater from Food Processing Industry: A Review. Imam J. Appl. Sci. 2017, 2, 27–36. [Google Scholar]
  31. Germirli, F.; Orhon, D.; Artan, N. Assessment of the Initial Inert Soluble COD in Industrial Wastewaters. Water Sci. Technol. 1991, 23, 1077–1086. [Google Scholar] [CrossRef]
  32. Choi, Y.-B.; Kwon, J.-H.; Rim, J.-M. Effect of Salt Concentration on the Aerobic Biodegradability of Sea Food Wastewater. J. Korean Soc. Environ. Eng. 2010, 32, 256–263. [Google Scholar]
  33. Van Ginkel, S.W.; Oh, S.-E.; Logan, B.E. Biohydrogen Gas Production from Food Processing and Domestic Wastewaters. Int. J. Hydrogen Energy 2005, 30, 1535–1542. [Google Scholar] [CrossRef]
  34. Liu, V.L.; Nakhla, G.; Bassi, A. Treatability and Kinetics Studies of Mesophilic Aerobic Biodegradation of High Oil and Grease Pet Food Wastewater. J. Hazard. Mater. 2004, 112, 87–94. [Google Scholar] [CrossRef]
  35. Bartolomeu, M.; Neves, M.; Faustino, M.A.F.; Almeida, A. Wastewater Chemical Contaminants: Remediation by Advanced Oxidation Processes. Photochem. Photobiol. Sci. 2018, 17, 1573–1598. [Google Scholar] [CrossRef]
  36. Khan, A.A.; Gul, J.; Naqvi, S.R.; Ali, I.; Farooq, W.; Liaqat, R.; AlMohamadi, H.; Štěpanec, L.; Juchelková, D. Recent Progress in Microalgae-Derived Biochar for the Treatment of Textile Industry Wastewater. Chemosphere 2022, 36, 135565. [Google Scholar] [CrossRef] [PubMed]
  37. García, V.; Pongrácz, E.; Phillips, P.S.; Keiski, R.L. From Waste Treatment to Resource Efficiency in the Chemical Industry: Recovery of Organic Solvents from Waters Containing Electrolytes by Pervaporation. J. Clean. Prod. 2013, 39, 146–153. [Google Scholar] [CrossRef]
  38. Patil, P.B.; Bhandari, V.M.; Ranade, V. V Wastewater Treatment and Process Intensification for Degradation of Solvents Using Hydrodynamic Cavitation. Chem. Eng. Process. Intensif. 2021, 166, 108485. [Google Scholar] [CrossRef]
  39. Abadi, S.R.H.; Sebzari, M.R.; Hemati, M.; Rekabdar, F.; Mohammadi, T. Ceramic Membrane Performance in Microfiltration of Oily Wastewater. Desalination 2011, 265, 222–228. [Google Scholar] [CrossRef]
  40. Diez, V.; Ramos, C.; Cabezas, J.L. Treating Wastewater with High Oil and Grease Content Using an Anaerobic Membrane Bioreactor (AnMBR). Filtration and Cleaning Assays. Water Sci. Technol. 2012, 65, 1847–1853. [Google Scholar] [CrossRef]
  41. Wang, B.; Wan, Y.; Gao, Y.; Zheng, G.; Yang, M.; Wu, S.; Hu, J. Occurrences and Behaviors of Naphthenic Acids in a Petroleum Refinery Wastewater Treatment Plant. Environ. Sci. Technol. 2015, 49, 5796–5804. [Google Scholar] [CrossRef] [PubMed]
  42. Guerrero, L.; Omil, F.; Mendez, R.; Lema, J.M. Protein Recovery during the Overall Treatment of Wastewaters from Fish-Meal Factories. Bioresour. Technol. 1998, 63, 221–229. [Google Scholar] [CrossRef]
  43. Momeni, M.M.; Kahforoushan, D.; Abbasi, F.; Ghanbarian, S. Using Chitosan/CHPATC as Coagulant to Remove Color and Turbidity of Industrial Wastewater: Optimization through RSM Design. J. Environ. Manag. 2018, 211, 347–355. [Google Scholar] [CrossRef]
  44. Khan, M.T.; Shah, I.A.; Ihsanullah, I.; Naushad, M.; Ali, S.; Shah, S.H.A.; Mohammad, A.W. Hospital Wastewater as a Source of Environmental Contamination: An Overview of Management Practices, Environmental Risks, and Treatment Processes. J. Water Process Eng. 2021, 41, 101990. [Google Scholar] [CrossRef]
  45. Yao, S.; Ye, J.; Yang, Q.; Hu, Y.; Zhang, T.; Jiang, L.; Munezero, S.; Lin, K.; Cui, C. Occurrence and Removal of Antibiotics, Antibiotic Resistance Genes, and Bacterial Communities in Hospital Wastewater. Environ. Sci. Pollut. Res. 2021, 28, 57321–57333. [Google Scholar] [CrossRef]
  46. Wang, J.; Shen, J.; Ye, D.; Yan, X.; Zhang, Y.; Yang, W.; Li, X.; Wang, J.; Zhang, L.; Pan, L. Disinfection Technology of Hospital Wastes and Wastewater: Suggestions for Disinfection Strategy during Coronavirus Disease 2019 (COVID-19) Pandemic in China. Environ. Pollut. 2020, 262, 114665. [Google Scholar] [CrossRef] [PubMed]
  47. Reichert, J.F.; Souza, D.M.; Martins, A.F. Antipsychotic Drugs in Hospital Wastewater and a Preliminary Risk Assessment. Ecotoxicol. Environ. Saf. 2019, 170, 559–567. [Google Scholar] [CrossRef]
  48. Aydin, S.; Aydin, M.E.; Ulvi, A.; Kilic, H. Antibiotics in Hospital Effluents: Occurrence, Contribution to Urban Wastewater, Removal in a Wastewater Treatment Plant, and Environmental Risk Assessment. Environ. Sci. Pollut. Res. 2019, 26, 544–558. [Google Scholar] [CrossRef] [PubMed]
  49. Cherni, Y.; Botta, C.; Kasmi, M.; Franciosa, I.; Cocolin, L.; Chatti, A.; Trabelsi, I.; Elleuch, L. Mixed Culture of Lactococcus Lactis and Kluyveromyces Marxianus Isolated from Kefir Grains for Pollutants Load Removal from Jebel Chakir Leachate. Water Environ. Res. 2020, 92, 2041–2048. [Google Scholar] [CrossRef]
  50. Chen, P.H.; Oswald, W.J.; Marsolek, M.D.; Kendall, E.; Thompson, P.L.; Shuman, T.R.; Prajapati, S.K.; Kaushik, P.; Malik, A.; Vijay, V.K.; et al. Algae Biorefinery—Concepts Microalgae—Microscopic Small “Plants”. Bioresour. Technol. 2013, 44, 471–474. [Google Scholar]
  51. Yang, Z.; Zhou, S. The Biological Treatment of Landfill Leachate Using a Simultaneous Aerobic and Anaerobic (SAA) Bio-Reactor System. Chemosphere 2008, 72, 1751–1756. [Google Scholar] [CrossRef] [PubMed]
  52. Samaei, S.M.; Gato-Trinidad, S.; Altaee, A. Performance Evaluation of Reverse Osmosis Process in the Post-Treatment of Mining Wastewaters: Case Study of Costerfield Mining Operations, Victoria, Australia. J. Water Process Eng. 2020, 34, 101116. [Google Scholar] [CrossRef]
  53. González-Muñoz, M.J.; Rodríguez, M.A.; Luque, S.; Álvarez, J.R. Recovery of Heavy Metals from Metal Industry Waste Waters by Chemical Precipitation and Nanofiltration. Desalination 2006, 200, 742–744. [Google Scholar] [CrossRef]
  54. Acheampong, M.A.; Meulepas, R.J.W.; Lens, P.N.L. Removal of Heavy Metals and Cyanide from Gold Mine Wastewater. J. Chem. Technol. Biotechnol. 2010, 85, 590–613. [Google Scholar] [CrossRef]
  55. Agarwal, S.; Darbar, S.; Saha, S. Challenges in Management of Domestic Wastewater for Sustainable Development. In Current Directions in Water Scarcity Research; Elsevier: Amsterdam, The Netherlands, 2022; Volume 6, pp. 531–552. ISBN 2542-7946. [Google Scholar]
  56. Badar, S.; Farooqi, I.H. Pulp and Paper Industry—Manufacturing Process, Wastewater Generation and Treatment. In Environmental Protection Strategies for Sustainable Development; Springer: Berlin/Heidelberg, Germany, 2012; pp. 397–436. [Google Scholar]
  57. Sharma, P.; Purchase, D.; Chandra, R. Residual Pollutants in Treated Pulp Paper Mill Wastewater and Their Phytotoxicity and Cytotoxicity in Allium Cepa. Environ. Geochem. Health 2021, 43, 2143–2164. [Google Scholar] [CrossRef]
  58. Devi, N.L.; Yadav, I.C.; Shihua, Q.I.; Singh, S.; Belagali, S.L. Physicochemical Characteristics of Paper Industry Effluents—A Case Study of South India Paper Mill (SIPM). Environ. Monit. Assess. 2011, 177, 23–33. [Google Scholar] [CrossRef] [PubMed]
  59. Müller, A.; Österlund, H.; Marsalek, J.; Viklander, M. The Pollution Conveyed by Urban Runoff: A Review of Sources. Sci. Total Environ. 2020, 709, 136125. [Google Scholar] [CrossRef] [PubMed]
  60. Kornboonraksa, T. Preliminary Study of Rapid Enhanced Effective Micro-Organisms (REEM) in Oil and Grease Trap from Canteen Wastewater. In Trends in Asian Water Environmental Science and Technology; Springer: Berlin/Heidelberg, Germany, 2016; pp. 71–80. [Google Scholar]
  61. Brown, J.N.; Peake, B.M. Sources of Heavy Metals and Polycyclic Aromatic Hydrocarbons in Urban Stormwater Runoff. Sci. Total Environ. 2006, 359, 145–155. [Google Scholar] [CrossRef] [PubMed]
  62. Fairbairn, D.J.; Elliott, S.M.; Kiesling, R.L.; Schoenfuss, H.L.; Ferrey, M.L.; Westerhoff, B.M. Contaminants of Emerging Concern in Urban Stormwater: Spatiotemporal Patterns and Removal by Iron-Enhanced Sand Filters (IESFs). Water Res. 2018, 145, 332–345. [Google Scholar] [CrossRef]
  63. Zhao, C.; Chen, W. A Review for Tannery Wastewater Treatment: Some Thoughts under Stricter Discharge Requirements. Environ. Sci. Pollut. Res. 2019, 26, 26102–26111. [Google Scholar] [CrossRef]
  64. Haroun, M.; Idris, A.; Omar, S.R.S. A Study of Heavy Metals and Their Fate in the Composting of Tannery Sludge. Waste Manag. 2007, 27, 1541–1550. [Google Scholar] [CrossRef]
  65. Ali, Z.; Malik, R.N.; Qadir, A. Heavy Metals Distribution and Risk Assessment in Soils Affected by Tannery Effluents. Chem. Ecol. 2013, 29, 676–692. [Google Scholar] [CrossRef]
  66. Vo, T.-D.-H.; Bui, X.-T.; Dang, B.-T.; Nguyen, T.-T.; Nguyen, V.-T.; Tran, D.P.H.; Nguyen, P.-T.; Boller, M.; Lin, K.-Y.A.; Varjani, S.; et al. Influence of Organic Loading Rates on Treatment Performance of Membrane Bioreactor Treating Tannery Wastewater. Environ. Technol. Innov. 2021, 24, 101810. [Google Scholar] [CrossRef]
  67. Hasegawa, M.C.; Daniel, J.F.d.S.; Takashima, K.; Batista, G.A.; da Silva, S.M.C.P. COD Removal and Toxicity Decrease from Tannery Wastewater by Zinc Oxide-Assisted Photocatalysis: A Case Study. Environ. Technol. 2014, 35, 1589–1595. [Google Scholar] [CrossRef]
  68. Jahan, M.A.A.; Akhtar, N.; Khan, N.M.S.; Roy, C.K.; Islam, R.; Nurunnabi, M. Characterization of Tannery Wastewater and Its Treatment by Aquatic Macrophytes and Algae. Bangladesh J. Sci. Ind. Res. 2015, 49, 233–242. [Google Scholar] [CrossRef]
  69. Arti; Mehra, R. Analysis of heavy metals and toxicity level in the tannery effluent and the environs. Environ. Monit. Assess. 2023, 195, 554. [Google Scholar] [CrossRef] [PubMed]
  70. Chatzisymeon, E.; Xekoukoulotakis, N.P.; Coz, A.; Kalogerakis, N.; Mantzavinos, D. Electrochemical Treatment of Textile Dyes and Dyehouse Effluents. J. Hazard. Mater. 2006, 137, 998–1007. [Google Scholar] [CrossRef] [PubMed]
  71. Sarker, M.R.; Chowdhury, M.; Deb, A.K. Reduction of Color Intensity from Textile Dye Wastewater Using Microorganisms: A Review. Int. J. Curr. Microbiol. Appl. Sci 2019, 8, 3407–3415. [Google Scholar] [CrossRef]
  72. Sarker, B.C.; Baten, M.A.; Eqram, M.; Haque, U.; Das, A.K.; Hossain, A.; Hasan, M.Z. Heavy Metals Concentration in Textile and Garments Industries’ Wastewater of Bhaluka Industrial Area, Mymensingh, Bangladesh. Curr. World Environ. 2015, 10, 61–66. [Google Scholar] [CrossRef]
  73. Nicolaou, M.; Hadjivassilis, I. Treatment of Wastewater from the Textile Industry. Water Sci. Technol. 1992, 25, 31–35. [Google Scholar] [CrossRef]
  74. Roy, R.; Fakhruddin, A.N.M.; Khatun, R.; Islam, M.S.; Ahsan, M.A.; Neger, A. Characterization of Textile Industrial Effluents and Its Effects on Aquatic Macrophytes and Algae. Bangladesh J. Sci. Ind. Res. 2010, 45, 79–84. [Google Scholar] [CrossRef]
  75. Alvim, C.B.; Bes-Piá, M.A.; Mendoza-Roca, J.A. Separation and Identification of Microplastics from Primary and Secondary Effluents and Activated Sludge from Wastewater Treatment Plants. Chem. Eng. J. 2020, 402, 126293. [Google Scholar] [CrossRef]
  76. Brown, A.K.; Wong, C.S. Distribution and Fate of Pharmaceuticals and Their Metabolite Conjugates in a Municipal Wastewater Treatment Plant. Water Res. 2018, 144, 774–783. [Google Scholar] [CrossRef]
  77. Raju, S.; Carbery, M.; Kuttykattil, A.; Senthirajah, K.; Lundmark, A.; Rogers, Z.; Suresh, S.C.B.; Evans, G.; Palanisami, T. Improved Methodology to Determine the Fate and Transport of Microplastics in a Secondary Wastewater Treatment Plant. Water Res. 2020, 173, 115549. [Google Scholar] [CrossRef]
  78. Kumar, R.; Sarmah, A.K.; Padhye, L.P. Fate of Pharmaceuticals and Personal Care Products in a Wastewater Treatment Plant with Parallel Secondary Wastewater Treatment Train. J. Environ. Manag. 2019, 233, 649–659. [Google Scholar] [CrossRef]
  79. Azuma, T.; Hayashi, T. On-Site Chlorination Responsible for Effective Disinfection of Wastewater from Hospital. Sci. Total Environ. 2021, 776, 145951. [Google Scholar] [CrossRef]
  80. Martin Ruel, S.; Choubert, J.-M.; Budzinski, H.; Miege, C.; Esperanza, M.; Coquery, M. Occurrence and Fate of Relevant Substances in Wastewater Treatment Plants Regarding Water Framework Directive and Future Legislations. Water Sci. Technol. 2012, 65, 1179–1189. [Google Scholar] [CrossRef]
  81. Salthammer, T. Emerging Indoor Pollutants. Int. J. Hyg. Environ. Health 2020, 224, 113423. [Google Scholar] [CrossRef]
  82. Arman, N.Z.; Salmiati, S.; Aris, A.; Salim, M.R.; Nazifa, T.H.; Muhamad, M.S.; Marpongahtun, M. A Review on Emerging Pollutants in the Water Environment: Existences, Health Effects and Treatment Processes. Water 2021, 13, 3258. [Google Scholar] [CrossRef]
  83. Yadav, D.; Rangabhashiyam, S.; Verma, P.; Singh, P.; Devi, P.; Kumar, P.; Hussain, C.M.; Gaurav, G.K.; Kumar, K.S. Environmental and Health Impacts of Contaminants of Emerging Concerns: Recent Treatment Challenges and Approaches. Chemosphere 2021, 272, 129492. [Google Scholar] [CrossRef]
  84. Wiering, M.; Boezeman, D.; Crabbé, A. The Water Framework Directive and Agricultural Diffuse Pollution: Fighting a Running Battle? Water 2020, 12, 1447. [Google Scholar] [CrossRef]
  85. Basis, L. Procedure File. Reading 2010, 2160, 8–10. [Google Scholar]
  86. Council, O.F.T.H.E. Directive 2013/11/EU of the European Parliament and of the Council. Fundam. Texts Eur. Priv. Law 2020, 2013, 1–17. [Google Scholar] [CrossRef]
  87. Ågerstrand, M.; Berg, C.; Björlenius, B.; Breitholtz, M.; Brunström, B.; Fick, J.; Gunnarsson, L.; Larsson, D.G.J.; Sumpter, J.P.; Tysklind, M. Improving Environmental Risk Assessment of Human Pharmaceuticals. Environ. Sci. Technol. 2015, 49, 5336–5345. [Google Scholar] [CrossRef] [PubMed]
  88. Available online: https://eur-lex.europa.eu/legal-content/en/ALL/?uri=CELEX%3A32006R1907 (accessed on 15 June 2024).
  89. Council, O.F.T.H.E. Regulation (EU) No 524/2013 of the European Parliament and of the Council. In Fundamental Texts on European Private Law; Hart Publishing: London, UK, 2020; pp. 1–123. [Google Scholar] [CrossRef]
  90. EMA. Guideline on the Environmental Risk Assessment of Medicinal Products for Human Use. Eur. Med. Agency 2006, 44, 1–48. [Google Scholar]
  91. Lapworth, D.J.; Lopez, B.; Laabs, V.; Kozel, R.; Wolter, R.; Ward, R.; Vargas Amelin, E.; Besien, T.; Claessens, J.; Delloye, F. Developing a Groundwater Watch List for Substances of Emerging Concern: A European Perspective. Environ. Res. Lett. 2019, 14, 35004. [Google Scholar] [CrossRef]
  92. Khan, S.; Naushad, M.; Govarthanan, M.; Iqbal, J.; Alfadul, S.M. Emerging Contaminants of High Concern for the Environment: Current Trends and Future Research. Environ. Res. 2022, 207, 112609. [Google Scholar] [CrossRef]
  93. FAO. The Future of Food and Agriculture—Alternative Pathways to 2050; FAO: Rome, Italy, 2018; ISBN 9789251301586. [Google Scholar]
  94. Nizami, A.-S.; Rehan, M.; Waqas, M.; Naqvi, M.; Ouda, O.K.M.; Shahzad, K.; Miandad, R.; Khan, M.Z.; Syamsiro, M.; Ismail, I.M.I. Waste Biorefineries: Enabling Circular Economies in Developing Countries. Bioresour. Technol. 2017, 241, 1101–1117. [Google Scholar] [CrossRef]
  95. Chaudry, S. Integrating Microalgae Cultivation with Wastewater Treatment: A Peek into Economics. Appl. Biochem. Biotechnol. 2021, 193, 3395–3406. [Google Scholar] [CrossRef] [PubMed]
  96. Mehariya, S.; Goswami, R.K.; Verma, P.; Lavecchia, R.; Zuorro, A. Integrated Approach for Wastewater Treatment and Biofuel Production in Microalgae Biorefineries. Energies 2021, 14, 2282. [Google Scholar] [CrossRef]
  97. El-Sheekh, M.; Abdel-Daim, M.M.; Okba, M.; Gharib, S.; Soliman, A.; El-Kassas, H. Green Technology for Bioremediation of the Eutrophication Phenomenon in Aquatic Ecosystems: A Review. Afr. J. Aquat. Sci. 2021, 46, 274–292. [Google Scholar] [CrossRef]
  98. Laraib, N.; Hussain, A.; Javid, A.; Hafeez-ur-Rehman, M.; Bukhari, S.M.; Rashid, M.; Ali, W. Recent Advancements in Microalgal-Induced Remediation of Wastewaters. In Microorganisms for Sustainable Environment and Health; Elsevier: Amsterdam, The Netherlands, 2020; pp. 205–217. [Google Scholar]
  99. Yaakob, M.A.; Mohamed, R.M.S.R.; Al-Gheethi, A.; Aswathnarayana Gokare, R.; Ambati, R.R. Influence of Nitrogen and Phosphorus on Microalgal Growth, Biomass, Lipid, and Fatty Acid Production: An Overview. Cells 2021, 10, 393. [Google Scholar] [CrossRef]
  100. Fazal, T.; Mushtaq, A.; Rehman, F.; Khan, A.U.; Rashid, N.; Farooq, W.; Rehman, M.S.U.; Xu, J. Bioremediation of Textile Wastewater and Successive Biodiesel Production Using Microalgae. Renew. Sustain. Energy Rev. 2018, 82, 3107–3126. [Google Scholar] [CrossRef]
  101. Sutherland, D.L.; Ralph, P.J. Microalgal Bioremediation of Emerging Contaminants-Opportunities and Challenges. Water Res. 2019, 164, 114921. [Google Scholar] [CrossRef]
  102. Xiong, J.-Q.; Kurade, M.B.; Jeon, B.-H. Biodegradation of Levofloxacin by an Acclimated Freshwater Microalga, Chlorella Vulgaris. Chem. Eng. J. 2017, 313, 1251–1257. [Google Scholar] [CrossRef]
  103. Leng, L.; Wei, L.; Xiong, Q.; Xu, S.; Li, W.; Lv, S.; Lu, Q.; Wan, L.; Wen, Z.; Zhou, W. Use of Microalgae Based Technology for the Removal of Antibiotics from Wastewater: A Review. Chemosphere 2020, 238, 124680. [Google Scholar] [CrossRef] [PubMed]
  104. Ding, T.; Yang, M.; Zhang, J.; Yang, B.; Lin, K.; Li, J.; Gan, J. Toxicity, Degradation and Metabolic Fate of Ibuprofen on Freshwater Diatom Navicula Sp. J. Hazard. Mater. 2017, 330, 127–134. [Google Scholar] [CrossRef] [PubMed]
  105. Brasil, B.d.S.A.F.; de Siqueira, F.G.; Salum, T.F.C.; Zanette, C.M.; Spier, M.R. Microalgae and Cyanobacteria as Enzyme Biofactories. Algal Res. 2017, 25, 76–89. [Google Scholar] [CrossRef]
  106. Priyadharshini, S.D.; Babu, P.S.; Manikandan, S.; Subbaiya, R.; Govarthanan, M.; Karmegam, N. Phycoremediation of Wastewater for Pollutant Removal: A Green Approach to Environmental Protection and Long-Term Remediation. Environ. Pollut. 2021, 290, 117989. [Google Scholar] [CrossRef]
  107. Xiong, J.-Q.; Kim, S.-J.; Kurade, M.B.; Govindwar, S.; Abou-Shanab, R.A.I.; Kim, J.-R.; Roh, H.-S.; Khan, M.A.; Jeon, B.-H. Combined Effects of Sulfamethazine and Sulfamethoxazole on a Freshwater Microalga, Scenedesmus Obliquus: Toxicity, Biodegradation, and Metabolic Fate. J. Hazard. Mater. 2019, 370, 138–146. [Google Scholar] [CrossRef] [PubMed]
  108. Xiong, Q.; Liu, Y.-S.; Hu, L.-X.; Shi, Z.-Q.; Cai, W.-W.; He, L.-Y.; Ying, G.-G. Co-Metabolism of Sulfamethoxazole by a Freshwater Microalga Chlorella Pyrenoidosa. Water Res. 2020, 175, 115656. [Google Scholar] [CrossRef]
  109. Vo, H.N.P.; Ngo, H.H.; Guo, W.; Nguyen, K.H.; Chang, S.W.; Nguyen, D.D.; Liu, Y.; Liu, Y.; Ding, A.; Bui, X.T. Micropollutants Cometabolism of Microalgae for Wastewater Remediation: Effect of Carbon Sources to Cometabolism and Degradation Products. Water Res. 2020, 183, 115974. [Google Scholar] [CrossRef]
  110. Mustafa, S.; Bhatti, H.N.; Maqbool, M.; Iqbal, M. Microalgae Biosorption, Bioaccumulation and Biodegradation Efficiency for the Remediation of Wastewater and Carbon Dioxide Mitigation: Prospects, Challenges and Opportunities. J. Water Process Eng. 2021, 41, 102009. [Google Scholar] [CrossRef]
  111. El-Sheekh, M.M.; Metwally, M.A.; Allam, N.; Hemdan, H.E. Simulation Treatment of Industrial Wastewater Using Microbiological Cell Immobilization Technique. Iran. J. Sci. Technol. Trans. A Sci. 2020, 44, 595–604. [Google Scholar] [CrossRef]
  112. Chia, W.Y.; Tang, D.Y.Y.; Khoo, K.S.; Lup, A.N.K.; Chew, K.W. Nature’s Fight against Plastic Pollution: Algae for Plastic Biodegradation and Bioplastics Production. Environ. Sci. Ecotechnol. 2020, 4, 100065. [Google Scholar] [CrossRef]
  113. Shanab, S.; Essa, A.; Shalaby, E. Bioremoval Capacity of Three Heavy Metals by Some Microalgae Species (Egyptian Isolates). Plant Signal. Behav. 2012, 7, 392–399. [Google Scholar] [CrossRef] [PubMed]
  114. Gunasundari, E. Adsorption Isotherm, Kinetics and Thermodynamic Analysis of Cu (II) Ions onto the Dried Algal Biomass (Spirulina Platensis). J. Ind. Eng. Chem. 2017, 56, 129–144. [Google Scholar]
  115. Wang, J.; Chen, C. Biosorbents for Heavy Metals Removal and Their Future. Biotechnol. Adv. 2009, 27, 195–226. [Google Scholar] [CrossRef] [PubMed]
  116. Neff, J.M. Bioaccumulation in Marine Organisms: Effect of Contaminants from Oil Well Produced Water; Elsevier: Amsterdam, The Netherlands, 2002; ISBN 0080527841. [Google Scholar]
  117. Mota, R.; Rossi, F.; Andrenelli, L.; Pereira, S.B.; De Philippis, R.; Tamagnini, P. Released Polysaccharides (RPS) from Cyanothece Sp. CCY 0110 as Biosorbent for Heavy Metals Bioremediation: Interactions between Metals and RPS Binding Sites. Appl. Microbiol. Biotechnol. 2016, 100, 7765–7775. [Google Scholar] [CrossRef]
  118. Rempel, A.; Gutkoski, J.P.; Nazari, M.T.; Biolchi, G.N.; Cavanhi, V.A.F.; Treichel, H.; Colla, L.M. Current Advances in Microalgae-Based Bioremediation and Other Technologies for Emerging Contaminants Treatment. Sci. Total Environ. 2021, 772, 144918. [Google Scholar] [CrossRef]
  119. Premaratne, M.; Nishshanka, G.; Liyanaarachchi, V.C.; Nimarshana, P.H.V.; Ariyadasa, T.U. Bioremediation of Textile Dye Wastewater Using Microalgae: Current Trends and Future Perspectives. J. Chem. Technol. Biotechnol. 2021, 96, 3249–3258. [Google Scholar] [CrossRef]
  120. Tamma, G.; Valenti, G.; Grossini, E.; Donnini, S.; Marino, A.; Marinelli, R.A.; Calamita, G. Aquaporin Membrane Channels in Oxidative Stress, Cell Signaling, and Aging: Recent Advances and Research Trends. Oxid. Med. Cell. Longev. 2018, 2018, 1501847. [Google Scholar] [CrossRef]
  121. Song, C.; Wei, Y.; Qiu, Y.; Qi, Y.; Li, Y.; Kitamura, Y. Biodegradability and Mechanism of Florfenicol via Chlorella Sp. UTEX1602 and L38: Experimental Study. Bioresour. Technol. 2019, 272, 529–534. [Google Scholar] [CrossRef] [PubMed]
  122. Rodea-Palomares, I.; Makowski, M.; Gonzalo, S.; González-Pleiter, M.; Leganés, F.; Fernández-Piñas, F. Effect of PFOA/PFOS Pre-Exposure on the Toxicity of the Herbicides 2, 4-D, Atrazine, Diuron and Paraquat to a Model Aquatic Photosynthetic Microorganism. Chemosphere 2015, 139, 65–72. [Google Scholar] [CrossRef]
  123. Saavedra, R.; Muñoz, R.; Taboada, M.E.; Bolado, S. Influence of Organic Matter and CO2 Supply on Bioremediation of Heavy Metals by Chlorella Vulgaris and Scenedesmus Almeriensis in a Multimetallic Matrix. Ecotoxicol. Environ. Saf. 2019, 182, 109393. [Google Scholar] [CrossRef]
  124. Su, Y. Revisiting Carbon, Nitrogen, and Phosphorus Metabolisms in Microalgae for Wastewater Treatment. Sci. Total Environ. 2021, 762, 144590. [Google Scholar] [CrossRef] [PubMed]
  125. Holmes, D.E.; Dang, Y.; Smith, J.A. Nitrogen Cycling during Wastewater Treatment. Adv. Appl. Microbiol. 2019, 106, 113–192. [Google Scholar] [PubMed]
  126. Raychaudhuric, S.; Simsekb, H.; Kumar, S. Algae-and Bacteria-Driven Technologies for Pharmaceutical Remediation in Wastewater. In Removal of Toxic Pollutants Through Microbiological and Tertiary Treatment; New Perspect; Elsevier: Amsterdam, The Netherlands, 2020; Volume 373. [Google Scholar]
  127. Mujtaba, G.; Lee, K. Advanced Treatment of Wastewater Using Symbiotic Co-Culture of Microalgae and Bacteria. Appl. Chem. Eng. 2016, 27, 1–9. [Google Scholar] [CrossRef]
  128. USEPA. Wastewater Management Fact Sheet; USEPA: Washington, DC, USA, 2007; pp. 1–7. [Google Scholar]
  129. Shah, M.P. Development in Wastewater Treatment Research and Processes: Advances in Industrial Wastewater Treatment Technologies: Removal of Contaminants and Recovery of Resources; Elsevier: Amsterdam, The Netherlands, 2023; ISBN 0323956858. [Google Scholar]
  130. Chen, D.; Cheng, Y.; Zhou, N.; Chen, P.; Wang, Y.; Li, K.; Huo, S.; Cheng, P.; Peng, P.; Zhang, R. Photocatalytic Degradation of Organic Pollutants Using TiO2-Based Photocatalysts: A Review. J. Clean. Prod. 2020, 268, 121725. [Google Scholar] [CrossRef]
  131. Nwoba, E.G.; Parlevliet, D.A.; Laird, D.W.; Alameh, K.; Moheimani, N.R. Pilot-Scale Self-Cooling Microalgal Closed Photobioreactor for Biomass Production and Electricity Generation. Algal Res. 2020, 45, 101731. [Google Scholar] [CrossRef]
  132. Saeed, M.U.; Hussain, N.; Sumrin, A.; Shahbaz, A.; Noor, S.; Bilal, M.; Aleya, L.; Iqbal, H.M.N. Microbial Bioremediation Strategies with Wastewater Treatment Potentialities—A Review. Sci. Total Environ. 2022, 818, 151754. [Google Scholar] [CrossRef]
  133. Ummalyma, S.B.; Mathew, A.K.; Pandey, A.; Sukumaran, R.K. Harvesting of Microalgal Biomass: Efficient Method for Flocculation through PH Modulation. Bioresour. Technol. 2016, 213, 216–221. [Google Scholar] [CrossRef]
  134. Chakraborty, M.; Miao, C.; McDonald, A.; Chen, S. Concomitant Extraction of Bio-Oil and Value Added Polysaccharides from Chlorella Sorokiniana Using a Unique Sequential Hydrothermal Extraction Technology. Fuel 2012, 95, 63–70. [Google Scholar] [CrossRef]
  135. Sutherland, D.L.; Howard-Williams, C.; Turnbull, M.H.; Broady, P.A.; Craggs, R.J. The Effects of CO2 Addition along a PH Gradient on Wastewater Microalgal Photo-Physiology, Biomass Production and Nutrient Removal. Water Res. 2015, 70, 9–26. [Google Scholar] [CrossRef] [PubMed]
  136. De-Bashan, L.E.; Bashan, Y. Immobilized Microalgae for Removing Pollutants: Review of Practical Aspects. Bioresour. Technol. 2010, 101, 1611–1627. [Google Scholar] [CrossRef]
  137. Wang, Z.; Xiu, G.; Qiao, T.; Zhao, K.; Zhang, D. Coupling Ozone and Hollow Fibers Membrane Bioreactor for Enhanced Treatment of Gaseous Xylene Mixture. Bioresour. Technol. 2013, 130, 52–58. [Google Scholar] [CrossRef]
  138. Hlongwane, G.N.; Sekoai, P.T.; Meyyappan, M.; Moothi, K. Simultaneous Removal of Pollutants from Water Using Nanoparticles: A Shift from Single Pollutant Control to Multiple Pollutant Control. Sci. Total Environ. 2019, 656, 808–833. [Google Scholar] [CrossRef] [PubMed]
  139. Sarkar, P.; Dey, A. Phycoremediation–an Emerging Technique for Dye Abatement: An Overview. Process Saf. Environ. Prot. 2021, 147, 214–225. [Google Scholar] [CrossRef]
  140. Frascaroli, G.; Hunter, C.; Roberts, J.; Escudero, A. Antibiotic Removal by Three Promising Microalgae Strains: Biotic, Abiotic Routes, and Response Mechanisms. Water, Air, Soil Pollut. 2024, 235, 600. [Google Scholar] [CrossRef]
  141. Hom-Diaz, A.; Jaén-Gil, A.; Rodríguez-Mozaz, S.; Barceló, D.; Vicent, T.; Blánquez, P. Insights into Removal of Antibiotics by Selected Microalgae (Chlamydomonas Reinhardtii, Chlorella Sorokiniana, Dunaliella Tertiolecta and Pseudokirchneriella Subcapitata). Algal Res. 2022, 61, 102560. [Google Scholar] [CrossRef]
  142. Lu, W.; Alam, M.A.; Liu, S.; Xu, J.; Saldivar, R.P. Critical Processes and Variables in Microalgae Biomass Production Coupled with Bioremediation of Nutrients and CO2 from Livestock Farms: A Review. Sci. Total Environ. 2020, 716, 135247. [Google Scholar] [CrossRef]
  143. Touliabah, H.E.-S.; El-Sheekh, M.M.; Ismail, M.M.; El-Kassas, H. A Review of Microalgae-and Cyanobacteria-Based Biodegradation of Organic Pollutants. Molecules 2022, 27, 1141. [Google Scholar] [CrossRef]
  144. Chan, S.S.; Khoo, K.S.; Chew, K.W.; Ling, T.C.; Show, P.L. Recent Advances Biodegradation and Biosorption of Organic Compounds from Wastewater: Microalgae-Bacteria Consortium-A Review. Bioresour. Technol. 2022, 344, 126159. [Google Scholar] [CrossRef]
  145. Campanella, L.; Cubadda, F.; Sammartino, M.P.; Saoncella, A. An Algal Biosensor for the Monitoring of Water Toxicity in Estuarine Environments. Water Res. 2001, 35, 69–76. [Google Scholar] [CrossRef]
  146. Vu, C.H.T.; Lee, H.-G.; Chang, Y.K.; Oh, H.-M. Axenic Cultures for Microalgal Biotechnology: Establishment, Assessment, Maintenance, and Applications. Biotechnol. Adv. 2018, 36, 380–396. [Google Scholar] [CrossRef]
  147. di Cicco, M.R.; Palmieri, M.; Altieri, S.; Ciniglia, C.; Lubritto, C. Cultivation of the Acidophilic Microalgae Galdieria Phlegrea with Wastewater: Process Yields. Int. J. Environ. Res. Public Health 2021, 18, 2291. [Google Scholar] [CrossRef] [PubMed]
  148. Spennati, E.; Casazza, A.A.; Converti, A. Winery Wastewater Treatment by Microalgae to Produce Low-Cost Biomass for Energy Production Purposes. Energies 2020, 13, 2490. [Google Scholar] [CrossRef]
  149. Ajayan, K.V.; Selvaraju, M.; Unnikannan, P.; Sruthi, P. Phycoremediation of Tannery Wastewater Using Microalgae Scenedesmus Species. Int. J. Phytoremed. 2015, 17, 907–916. [Google Scholar] [CrossRef]
  150. Daneshvar, E.; Zarrinmehr, M.J.; Hashtjin, A.M.; Farhadian, O.; Bhatnagar, A. Versatile Applications of Freshwater and Marine Water Microalgae in Dairy Wastewater Treatment, Lipid Extraction and Tetracycline Biosorption. Bioresour. Technol. 2018, 268, 523–530. [Google Scholar] [CrossRef]
  151. Blanco-Vieites, M.; Suárez-Montes, D.; Hernández Battez, A.; Rodríguez, E. Enhancement of Arthrospira Sp. Culturing for Sulfate Removal and Mining Wastewater Bioremediation. Int. J. Phytoremed. 2023, 25, 1116–1126. [Google Scholar] [CrossRef]
  152. Salgado, E.M.; Gonçalves, A.L.; Sánchez-Soberón, F.; Ratola, N.; Pires, J.C.M. Microalgal Cultures for the Bioremediation of Urban Wastewaters in the Presence of Siloxanes. Int. J. Environ. Res. Public Health 2022, 19, 2634. [Google Scholar] [CrossRef]
  153. Papadopoulos, K.P.; Economou, C.N.; Tekerlekopoulou, A.G.; Vayenas, D. V Two-Step Treatment of Brewery Wastewater Using Electrocoagulation and Cyanobacteria-Based Cultivation. J. Environ. Manag. 2020, 265, 110543. [Google Scholar] [CrossRef] [PubMed]
  154. Sayara, T.; Khayat, S.; Saleh, J.; Van Der Steen, P. Bioremediation of Nutrients from Municipal Wastewater Using Algal-Bacterial Photobioreactor: Real Field Scale Demonstration for Improving Effluent Quality. J. Water Chem. Technol. 2021, 43, 261–268. [Google Scholar] [CrossRef]
  155. Mubashar, M.; Naveed, M.; Mustafa, A.; Ashraf, S.; Shehzad Baig, K.; Alamri, S.; Siddiqui, M.H.; Zabochnicka-Świątek, M.; Szota, M.; Kalaji, H.M. Experimental Investigation of Chlorella Vulgaris and Enterobacter Sp. MN17 for Decolorization and Removal of Heavy Metals from Textile Wastewater. Water 2020, 12, 3034. [Google Scholar] [CrossRef]
  156. Lima, S.; Villanova, V.; Grisafi, F.; Caputo, G.; Brucato, A.; Scargiali, F. Autochthonous Microalgae Grown in Municipal Wastewaters as a Tool for Effectively Removing Nitrogen and Phosphorous. J. Water Process Eng. 2020, 38, 101647. [Google Scholar] [CrossRef]
  157. Serrà, A.; Artal, R.; García-Amorós, J.; Gómez, E.; Philippe, L. Circular Zero-Residue Process Using Microalgae for Efficient Water Decontamination, Biofuel Production, and Carbon Dioxide Fixation. Chem. Eng. J. 2020, 388, 124278. [Google Scholar] [CrossRef]
  158. Encarnação, T.; Palito, C.; Pais, A.A.C.C.; Valente, A.J.M.; Burrows, H.D. Removal of Pharmaceuticals from Water by Free and Imobilised Microalgae. Molecules 2020, 25, 3639. [Google Scholar] [CrossRef]
  159. El-Kassas, H.Y.; Mohamed, L.A. Bioremediation of the Textile Waste Effluent by Chlorella Vulgaris. Egypt. J. Aquat. Res. 2014, 40, 301–308. [Google Scholar] [CrossRef]
  160. Chisti, Y. Raceways-Based Production of Algal Crude Oil. Green 2013, 3, 195–216. [Google Scholar] [CrossRef]
  161. Fernández, F.G.A.; Sevilla, J.M.F.; Grima, E.M. Costs Analysis of Microalgae Production. In Biofuels from Algae; Elsevier: Amsterdam, The Netherlands, 2019; pp. 551–566. [Google Scholar]
  162. Moreno-Garcia, L.; Adjallé, K.; Barnabé, S.; Raghavan, G.S. V Microalgae Biomass Production for a Biorefinery System: Recent Advances and the Way towards Sustainability. Renew. Sustain. Energy Rev. 2017, 76, 493–506. [Google Scholar] [CrossRef]
  163. Abdel-Raouf, N.; Al-Homaidan, A.A.; Ibraheem, I. Microalgae and Wastewater Treatment. Saudi J. Biol. Sci. 2012, 19, 257–275. [Google Scholar] [CrossRef]
  164. Borowitzka, M.A. High-Value Products from Microalgae-Their Development and Commercialisation. J. Appl. Phycol. 2013, 25, 743–756. [Google Scholar] [CrossRef]
  165. Abdelfattah, A.; Ali, S.S.; Ramadan, H.; El-Aswar, E.I.; Eltawab, R.; Ho, S.-H.; Elsamahy, T.; Li, S.; El-Sheekh, M.M.; Schagerl, M. Microalgae-Based Wastewater Treatment: Mechanisms, Challenges, Recent Advances, and Future Prospects. Environ. Sci. Ecotechnol. 2023, 13, 100205. [Google Scholar] [CrossRef]
  166. Kensa, V.M. Bioremediation-an Overview. J. Ind. Pollut. Control 2011, 27, 161–168. [Google Scholar]
  167. Withers, P.J.A.; Elser, J.J.; Hilton, J.; Ohtake, H.; Schipper, W.J.; Van Dijk, K.C. Greening the Global Phosphorus Cycle: How Green Chemistry Can Help Achieve Planetary P Sustainability. Green Chem. 2015, 17, 2087–2099. [Google Scholar] [CrossRef]
  168. Mata, T.M.; Martins, A.A.; Caetano, N.S. Microalgae for Biodiesel Production and Other Applications: A Review. Renew. Sustain. Energy Rev. 2010, 14, 217–232. [Google Scholar] [CrossRef]
  169. Ruiz, J.; Olivieri, G.; De Vree, J.; Bosma, R.; Willems, P.; Reith, J.H.; Eppink, M.H.M.; Kleinegris, D.M.M.; Wijffels, R.H.; Barbosa, M.J. Towards Industrial Products from Microalgae. Energy Environ. Sci. 2016, 9, 3036–3043. [Google Scholar] [CrossRef]
  170. Montégut, L.; de Cabo, R.; Zitvogel, L.; Kroemer, G. Science-Driven Nutritional Interventions for the Prevention and Treatment of Cancer. Cancer Discov. 2022, 12, 2258–2279. [Google Scholar] [CrossRef]
  171. Becker, E.W. Micro-Algae as a Source of Protein. Biotechnol. Adv. 2007, 25, 207–210. [Google Scholar] [CrossRef]
  172. Mulbry, W.; Westhead, E.K.; Pizarro, C.; Sikora, L. Recycling of Manure Nutrients: Use of Algal Biomass from Dairy Manure Treatment as a Slow Release Fertilizer. Bioresour. Technol. 2005, 96, 451–458. [Google Scholar] [CrossRef]
  173. Gondi, R.; Kavitha, S.; Yukesh Kannah, R.; Parthiba Karthikeyan, O.; Kumar, G.; Kumar Tyagi, V.; Rajesh Banu, J. Algal-Based System for Removal of Emerging Pollutants from Wastewater: A Review. Bioresour. Technol. 2022, 344, 126245. [Google Scholar] [CrossRef] [PubMed]
  174. Talukder, M.M.R.; Das, P.; Wu, J.C. Microalgae (Nannochloropsis Salina) Biomass to Lactic Acid and Lipid. Biochem. Eng. J. 2012, 68, 109–113. [Google Scholar] [CrossRef]
  175. Rocha, C.J.L.; Álvarez-Castillo, E.; Yáñez, M.R.E.; Bengoechea, C.; Guerrero, A.; Ledesma, M.T.O. Development of Bioplastics from a Microalgae Consortium from Wastewater. J. Environ. Manag. 2020, 263, 110353. [Google Scholar] [CrossRef] [PubMed]
  176. Eriksen, N.T. Production of Phycocyanin—A Pigment with Applications in Biology, Biotechnology, Foods and Medicine. Appl. Microbiol. Biotechnol. 2008, 80, 1–14. [Google Scholar] [CrossRef]
  177. Adarme-Vega, T.C.; Lim, D.K.Y.; Timmins, M.; Vernen, F.; Li, Y.; Schenk, P.M. Microalgal Biofactories: A Promising Approach towards Sustainable Omega-3 Fatty Acid Production. Microb. Cell Fact. 2012, 11, 96. [Google Scholar] [CrossRef]
  178. Del Campo, J.A.; García-González, M.; Guerrero, M.G. Outdoor Cultivation of Microalgae for Carotenoid Production: Current State and Perspectives. Appl. Microbiol. Biotechnol. 2007, 74, 1163–1174. [Google Scholar] [CrossRef] [PubMed]
  179. Nwoba, E.G.; Ogbonna, C.N.; Ishika, T.; Vadiveloo, A. Microalgal Pigments: A Source of Natural Food Colors. In Microalgae Biotechnology for Food, Health and High Value Products; Springer: Berlin/Heidelberg, Germany, 2020; pp. 81–123. [Google Scholar]
  180. Delrue, F.; Setier, P.-A.; Sahut, C.; Cournac, L.; Roubaud, A.; Peltier, G.; Froment, A.-K. An Economic, Sustainability, and Energetic Model of Biodiesel Production from Microalgae. Bioresour. Technol. 2012, 111, 191–200. [Google Scholar] [CrossRef] [PubMed]
  181. Chaput, G.; Charmanski, K.; Farag, I. Sustainable Production of Microalgae Oil Feedstock Using Municipal Wastewater and CO2 Fertilization. Int. J. Eng. Sci. Technol. 2012, 4, 3489–3499. [Google Scholar]
  182. Pittman, J.K.; Dean, A.P.; Osundeko, O. The Potential of Sustainable Algal Biofuel Production Using Wastewater Resources. Bioresour. Technol. 2011, 102, 17–25. [Google Scholar] [CrossRef] [PubMed]
  183. Park, J.B.K.; Craggs, R.J.; Shilton, A.N. Wastewater Treatment High Rate Algal Ponds for Biofuel Production. Bioresour. Technol. 2011, 102, 35–42. [Google Scholar] [CrossRef] [PubMed]
  184. Acién, F.G.; Fernández, J.M.; Magán, J.J.; Molina, E. Production Cost of a Real Microalgae Production Plant and Strategies to Reduce It. Biotechnol. Adv. 2012, 30, 1344–1353. [Google Scholar] [CrossRef]
  185. Oostlander, P.C.; van Houcke, J.; Wijffels, R.H.; Barbosa, M.J. Microalgae Production Cost in Aquaculture Hatcheries. Aquaculture 2020, 525, 735310. [Google Scholar] [CrossRef]
  186. Uduman, N.; Qi, Y.; Danquah, M.K.; Forde, G.M.; Hoadley, A. Dewatering of Microalgal Cultures: A Major Bottleneck to Algae-Based Fuels. J. Renew. Sustain. Energy 2010, 2, 012701. [Google Scholar] [CrossRef]
  187. Halim, R.; Danquah, M.K.; Webley, P.A. Extraction of Oil from Microalgae for Biodiesel Production: A Review. Biotechnol. Adv. 2012, 30, 709–732. [Google Scholar] [CrossRef]
  188. Brennan, L.; Owende, P. Biofuels from Microalgae-A Review of Technologies for Production, Processing, and Extractions of Biofuels and Co-Products. Renew. Sustain. Energy Rev. 2010, 14, 557–577. [Google Scholar] [CrossRef]
  189. Abdelaziz, A.E.M.; Leite, G.B.; Belhaj, M.A.; Hallenbeck, P.C. Screening Microalgae Native to Quebec for Wastewater Treatment and Biodiesel Production. Bioresour. Technol. 2014, 157, 140–148. [Google Scholar] [CrossRef] [PubMed]
  190. Bhatt, A.H.; Tao, L. Economic Perspectives of Biogas Production via Anaerobic Digestion. Bioengineering 2020, 7, 74. [Google Scholar] [CrossRef]
  191. Borazjani, Z.; Bayat Mastalinezhad, F.; Azin, R.; Osfouri, S. Global Perspective of Hydrothermal Liquefaction of Algae: A Review of the Process, Kinetics, and Economics Analysis. BioEnergy Res. 2023, 16, 1493–1511. [Google Scholar] [CrossRef]
  192. Biller, P.; Ross, A.B.; Skill, S.C.; Lea-Langton, A.; Balasundaram, B.; Hall, C.; Riley, R.; Llewellyn, C.A. Nutrient Recycling of Aqueous Phase for Microalgae Cultivation from the Hydrothermal Liquefaction Process. Algal Res. 2012, 1, 70–76. [Google Scholar] [CrossRef]
  193. Garcia Alba, L.; Torri, C.; Samorì, C.; Van Der Spek, J.; Fabbri, D.; Kersten, S.R.A.; Brilman, D.W.F. Hydrothermal Treatment (HTT) of Microalgae: Evaluation of the Process as Conversion Method in an Algae Biorefinery Concept. Energy Fuels 2012, 26, 642–657. [Google Scholar] [CrossRef]
  194. Hognon, C.; Delrue, F.; Texier, J.; Grateau, M.; Thiery, S.; Miller, H.; Roubaud, A. Comparison of Pyrolysis and Hydrothermal Liquefaction of Chlamydomonas Reinhardtii. Growth Studies on the Recovered Hydrothermal Aqueous Phase. Biomass Bioenergy 2015, 73, 23–31. [Google Scholar] [CrossRef]
  195. 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]
  196. Bird, M.I.; Wurster, C.M.; de Paula Silva, P.H.; Paul, N.A.; De Nys, R. Algal Biochar: Effects and Applications. Gcb Bioenergy 2012, 4, 61–69. [Google Scholar] [CrossRef]
  197. Agrafioti, E.; Bouras, G.; Kalderis, D.; Diamadopoulos, E. Biochar Production by Sewage Sludge Pyrolysis. J. Anal. Appl. Pyrolysis 2013, 101, 72–78. [Google Scholar] [CrossRef]
  198. Wijffels, R.H.; Kruse, O.; Hellingwerf, K.J. Potential of Industrial Biotechnology with Cyanobacteria and Eukaryotic Microalgae. Curr. Opin. Biotechnol. 2013, 24, 405–413. [Google Scholar] [CrossRef]
  199. Milledge, J.J. Commercial Application of Microalgae Other than as Biofuels: A Brief Review. Rev. Environ. Sci. Bio/Technol. 2011, 10, 31–41. [Google Scholar] [CrossRef]
  200. de la Noüe, J.; Laliberté, G.; Proulx, D. Algae and Waste Water. J. Appl. Phycol. 1992, 4, 247–254. [Google Scholar] [CrossRef]
  201. Costa, J.A.V.; Freitas, B.C.B.; Rosa, G.M.; Moraes, L.; Morais, M.G.; Mitchell, B.G. Operational and Economic Aspects of Spirulina-Based Biorefinery. Bioresour. Technol. 2019, 292, 121946. [Google Scholar] [CrossRef] [PubMed]
  202. Feng, Y.; Li, C.; Zhang, D. Lipid Production of Chlorella Vulgaris Cultured in Artificial Wastewater Medium. Bioresour. Technol. 2011, 102, 101–105. [Google Scholar] [CrossRef] [PubMed]
  203. Pavithra, K.G.; Kumar, P.S.; Jaikumar, V.; Vardhan, K.H.; SundarRajan, P. Microalgae for Biofuel Production and Removal of Heavy Metals: A Review. Environ. Chem. Lett. 2020, 18, 1905–1923. [Google Scholar] [CrossRef]
  204. Corominas, L.; Garrido-Baserba, M.; Villez, K.; Olsson, G.; Cortés, U.; Poch, M. Transforming Data into Knowledge for Improved Wastewater Treatment Operation: A Critical Review of Techniques. Environ. Model. Softw. 2018, 106, 89–103. [Google Scholar] [CrossRef]
  205. Yellapu, S.K.; Klai, N.; Kaur, R.; Tyagi, R.D.; Surampalli, R.Y. Oleaginous Yeast Biomass Flocculation Using Bioflocculant Produced in Wastewater Sludge and Transesterification Using Petroleum Diesel as a Co-Solvent. Renew. Energy 2019, 131, 217–228. [Google Scholar] [CrossRef]
Table 1. Types of WW and main present pollutants.
Table 1. Types of WW and main present pollutants.
WastewaterDescriptionMain PollutantsAmountRef.
AgriculturalWastewater resulting from agricultural activitiesNutrientsNitrogen≈18–448 mg/L[10,11,12,13,14,15,16,17,18,19]
Phosphorus≈5.4–7.1 mg/L
Pesticides and herbicidesFluconazole, diazinon, diuron, atrazine, simazine, and malathion, metalochlor, tebuconazole tebuconazole and carbendazim≈3 ng/L–27 μg/L
Organic matterChemical Oxygen Demand (COD)≈1–30 g/L
DairyWastewater generated from dairy farms and processing facilitiesOrganic matterCOD≈1–7.5 g/L[20,21,22,23,24]
NutrientsNitrogen≈19.5–57.2 g/kg
Phosphorous≈20–65.9 g/kg
Potassium≈2.9–7.3 g/kg
DomesticWastewater generated from households, including sewage and waterborne wastes from kitchens, bathrooms, and toiletsBiodegradable and non-biodegradable organic matterFibers≈20.6%[9,25,26,27,28,29]
Sugars≈10.7%
Proteins≈12.4%
Soap and detergentsAlkylbenzene sulfonate≈39 μg/L
Alcohol ethoxylate≈6.2 μg/L
Alcohol ethoxy sulfate≈6.5 μg/L
Alcohol sulfate≈5.7 μg/L
Soap≈174 μg/L
Pathogenic microorganismsClostridium, Klebsiella, Corynebacterium, Bordetella, Staphylococcus and Rhodococcus≈1.5–5 log units
Pharmaceuticals and personal care productsCaffeine≈61 μg/L
Ibuprofen≈1.2 μg/L
Atenolol≈2.9 μg/L
Triclocarban≈2.4 μg/L
Suspended solids≈120 mg/L
Food processingWastewater from food processing plantsOrganic matterCOD≈1–9 g/L[30,31,32,33,34]
Biological Oxygen Demand (BOD)≈9–20 g/L
IndustrialWastewater produced by industrial processes contains a variety of chemicals and contaminants specific to the industryOil and grease≈50–66 mg/L≈500 mg/kg[35,36,37,38,39,40,41,42,43]
Process and cooling water
Oils and grease≈4–6000 mg/L
Organic matterTotal organic compound≈100 and 3000 mg/L
Total naphthenic acids≈113–392 μg/L
COD≈22 g/L
BOD≈10 g/L
Suspend solids≈0.5–40 mg/L
Colorants and dyes>1000 mg/L
Solventsn-butanol dichloromethane, octanol, dimethyl formamide, and cyclohexanol≈50–200 mg/L
HospitalWastewater generated in healthcare facilitiesPathogenic microorganismsAcinetobacter
Klebsiella
Aeromonas
Pseudomonas.
[44,45,46,47,48]
Chemical disinfectantsPovidone-iodine≈0.4 ppm
Liquid chlorine
Sodium hypochlorite
Chlorine dioxide
PharmaceuticalsClozapine, chlorpromazine and risperidone≈0.310–1432 μg/L
AntibioticsAzithromycin, clarithromycin, and ciprofloxacin≈21.2–4886 ng/L
LeachateLiquid that percolates through a landfill site, picking up contaminants from decomposing waste materialsOrganic matterCOD≈3.8–28 g/L[49,50,51]
BOD≈1–11 g/L
Suspended solids ≈850–5840 mg/L
Toxic chemicalsVery different composition depending on which wastes are present in the landfill
Ammonia ≈1040–3560 mg/L
MiningWastewater produced by mining operationsHeavy metalsArsenic, Cadmium, Lead, Selenium, Iron and Zinc≈200 g/L[52,53,54]
Acidic pH <3.6
Suspended solids ≈22 mg/L
Dissolved solids ≈2900 mg/L
Municipal/UrbanMixture of domestic wastewater with industrial wastewater and/or runoff rainwaterSimilar components to domestic wastewater with potential industrial additives [55]
Paper and pulp millWastewater from paper and pulp manufacturing facilitiesNutrientsTotal phenol≈39 mg/L[56,57,58]
Nitrogen≈125–234 mg/L
Sulfate≈1926–2098 mg/L
Organic matterCOD≈17.9–19 g/L
Chlorinated compounds ≈3.12–5.43 mg/L
Suspend solids ≈80–90 mg/L
Dissolved solids ≈1 g/L
Solvents ≈0.4–3 g/L
StormwaterRainwater runoff from precipitation eventsOil and grease>4–800 mg/L[39,59,60,61,62]
Heavy metalsLead≈119–527 μg/g
Copper≈50–464 μg/g
Zinc≈241–1325 μg/g
Fertilizers and pesticides≈0.1–10 ng/L
TanneryWastewater produced by tanneriesHeavy metalsChromium, Cadmium, Cobalt and Lead≈500 mg/kg[63,64,65,66,67,68,69]
Organic matterCOD≈1.3–2.6 kg/d
Suspended solids ≈1.2–28 g/L
High salinity ≈13.8 mg/L
TextileWastewater from the textile and garment industryDyes and colorants≈10–361 mg/L[70,71,72,73,74]
Heavy metalsCopper≈0.0405 ppm
Lead≈0.0003 ppm
Organic matterCOD≈240 kg/d
BOD≈60 kg/d
Suspended solids≈100–336 mg/L
Dissolved solids≈1.8–4.4 g/L
Table 2. Studies of microalgae-based treatments for the removal of pollutants from WWs and subsequent application of the produced biomass.
Table 2. Studies of microalgae-based treatments for the removal of pollutants from WWs and subsequent application of the produced biomass.
StrainsType of WWVolume Treated (L)Exp Time (Day)PollutantsRemoval RateBiomass
Application
Ref.
Consortium of Chlorella vulgaris, Scenedesmus quadricauda and Arthrospira platensisUrban WW1028Malathion99%/[7]
Agricultural drainageCadmium88%
Combination of bothNickel95%
Lead89%
Galdieria phlegreaUrban WW19Ammonium≈70%/[147]
Phosphates≈22%
Co-culture of Chlorella vulgaris and Arthrospira platensisWinery WW0.215Polyphenols50%Biofuel[148]
Scenedesmus sp.Tannery WW0.2512Chromiumup to 96%/[149]
Copperup to 98%
Zincup to 98%
Leadup to 98%
Scenedesmus quadricauda and Tetraselmis suecicaDairy WW1012Nitrates≈95%Tetracycline bioadsorption ≈ 70%[150]
Phosphates≈89%
Sulfate100%
Chlorella pyrenoidosa, Chlamydomonas reinhardtii,
Scenedesmus obliquus and Chlorella vulgaris
Domestic WW17Mercury>50%/[6]
Lead>50%
Gold>50%
Silver>50%
Manganese>50%
Clarithromycin80%
Roxithromycin>50%
Triclocarban>50%
Chlorella pyrenoidosaTextile WW17Indigo dye89%/[119]
Direct blue dye79%
Remazol brilliant orange75%
Crystal violet dye72%
Arthrospira platensis and Arthrospira maximaMining WW0.512Sulfate73%/[151]
Nitrogenup to 86%
Phopshorousup to 80%
C. vulgarisUrban WW4.59Siloxane≈98%/[152]
Leptolyngbya sp. and ChroococcusBrewery WW115Nitrates67%Bioethanol production[153]
Ammonium98%
Total Phosphorous75%
Natural BloomDomestic WW6030Ammonium55%/[154]
Total Phosphorous91%
Chlorella vulgaris and Scenedesmus almeriensisSynthetic WW0.53Arsenicup to 35%/[123]
Copperup to 98%
Manganeseup to 78%
Zincup to 83%
Enterobacter sp. MN17 and Chlorella vulgarisTextile WW55Cadmium93%Bioenergy production[155]
Chromium79%
Copper72%
Lead79%
Nannochloropsis gaditana, Chlorella sorokiniana, Chlorella sp. and Dunaliella tertiolectaMunicipal WW0.115Total Nitrogen77%Biostimulants, biofuels, bioplastics, Syngas[156]
Total Phosphorous61%
Arthrospira platensisIndustrial WW308Copper68%Bioethanol[157]
Nickel75%
Zinc42%
Chromium24%
Nannochloropsis sp.Synthetic WW26Paracetamol≈50%Biobased feedstock[158]
Ibuprofen≈50%
Olanzapine≈50%
Simvastatin≈50%
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Liberti, D.; Pinheiro, F.; Simões, B.; Varela, J.; Barreira, L. Beyond Bioremediation: The Untapped Potential of Microalgae in Wastewater Treatment. Water 2024, 16, 2710. https://doi.org/10.3390/w16192710

AMA Style

Liberti D, Pinheiro F, Simões B, Varela J, Barreira L. Beyond Bioremediation: The Untapped Potential of Microalgae in Wastewater Treatment. Water. 2024; 16(19):2710. https://doi.org/10.3390/w16192710

Chicago/Turabian Style

Liberti, Davide, Filipa Pinheiro, Beatriz Simões, João Varela, and Luísa Barreira. 2024. "Beyond Bioremediation: The Untapped Potential of Microalgae in Wastewater Treatment" Water 16, no. 19: 2710. https://doi.org/10.3390/w16192710

APA Style

Liberti, D., Pinheiro, F., Simões, B., Varela, J., & Barreira, L. (2024). Beyond Bioremediation: The Untapped Potential of Microalgae in Wastewater Treatment. Water, 16(19), 2710. https://doi.org/10.3390/w16192710

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