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Microplastic removal from wastewater through biopolymer and nanocellulose-based green technologies

Sayam Sayam a, Tarikul Islam *bc, Tasnim Hanan Tusti d and Joyjit Ghosh c
aDepartment of Fabric Engineering, Barishal Textile Engineering College, Barishal 8200, Bangladesh
bDepartment of Textile Engineering, Jashore University of Science and Technology, Jashore 7408, Bangladesh
cDepartment of Textiles, Merchandising, and Interiors, University of Georgia, Athens, Georgia 30602, USA. E-mail: tarikul@uga.edu
dDepartment of Civil Engineering, Khulna University of Engineering & Technology, Khulna 9203, Bangladesh

Received 30th July 2025 , Accepted 27th October 2025

First published on 28th October 2025


Abstract

Microplastics (MPs) in wastewater are a growing environmental issue that needs effective solutions. This review examines the use of nanocellulose and biopolymers as sustainable options for removing these pollutants from water. Nanocellulose (NC) is efficient due to its large surface area and biodegradable nature, achieving up to 98% removal of microplastics through various processes, including adsorption and filtration. Similarly, biopolymers like polysaccharides, lignin, and pectin can remove up to 99% of particles by clumping and settling them out. However, some microplastics are not easily removed by these materials on their own. Combining different materials, such as cellulose and chitosan, can enhance removal efficiency to about 75%. Integrating these solutions into existing wastewater treatment plants could help reduce microplastics and save costs; however, it is essential to ensure compatibility with current systems and establish appropriate regulations. The review also highlights the need for future research to support the widespread use of these methods in water treatment.



Sustainability spotlight

This review addresses the sustainability challenges associated with microplastic contamination in wastewater and highlights green technologies for their removal. It focuses on nanocellulose and biopolymer-based materials derived from renewable resources, emphasizing their biodegradability, low toxicity, and potential to replace synthetic treatment agents. The paper evaluates the environmental benefits of adsorption, coagulation, and filtration mechanisms compared to conventional chemical methods, outlining strategies to reduce secondary pollution and energy demand. By exploring scalable integration into existing wastewater treatment systems, this review offers a pathway toward sustainable water management practices aligned with circular economy principles.

1. Introduction

Plastic materials first appeared in the late 19th century, with commercial use beginning in 1870.1 Due to their light weight, durability, and corrosion resistance, plastics have rapidly gained popularity across various industries. As a result, plastic production increased nearly 180 times between 1950 and 2018, reaching over 400.3 million tons globally by 2022.2 These synthetic macromolecular polymers, such as polyethylene terephthalate, polyethylene, polypropylene, polyvinyl chloride, polyamides, polystyrene, and polyurethanes, have become indispensable in daily life,3–5 especially in sectors like textiles, construction, motor vehicles, consumer goods, medical, and food packaging.6,7 A detailed overview of plastic evolution and its key historical milestones is presented in Fig. 1.8
image file: d5su00634a-f1.tif
Fig. 1 Historical timeline depicting the development and use of plastics (created with MS PowerPoint).

Among these sectors, the textile industry is a leading consumer of synthetic polymers. Since 1995, synthetic fibers have surpassed cotton as the most widely used textile material, accounting for approximately 65% of global fiber production by 2020.9 China and India dominate this sector, accounting for 66% and 8% of global output, respectively, followed by Taiwan and the United States, each at approximately 4%.10,11 However, the widespread use of synthetic fibers has led to increasing environmental concerns, particularly regarding MP pollution. Synthetic fibers shed MPs during washing and wear, contributing significantly to the presence of MPs in water bodies. These particles often end up in wastewater treatment systems, where they persist due to their resistance to degradation.

The rising accumulation of plastic waste, primarily from single-use products such as shopping bags, bottles, and lids, has exacerbated global pollution issues.7,12 While some plastics, such as bottles, are recyclable, most single-use items still accumulate in landfills or are incinerated, adding to environmental degradation.13,14 Plastic pollution has now been reported in a variety of ecosystems, including coastlines,15 oceans,16 deep-sea areas,17 and even remote islands.18 Plastics degrade into MPs, which are categorized into primary and secondary types.19–21 Primary MPs are intentionally produced in small sizes (2 to 5 mm), often found in products such as microbeads in cosmetics,21–23 whereas secondary MPs result from the fragmentation of larger plastics through physical abrasion or UV radiation.22–24 These degradation processes can produce particles as small as 1.6 µm, which have been detected in marine environments.25,26 Interestingly, the concentration of MPs in surface ocean waters is lower than expected due to their tendency to aggregate with marine particles and settle into sediments, often facilitated by biofilm formation.27

Wastewater treatment plants (WWTPs) are significant entry points for MPs into the environment. According to Sun et al.,5 MP concentrations in WWTP effluents can reach up to 447 particles per liter, with polystyrene (PS) being among the most detected polymers. Even with tertiary treatment processes (TTPs), effluents may still contain up to 51 particles per liter, and only 24% of WWTPs globally currently implement TTPs. Consequently, daily median MP discharges can reach approximately 2 million particles.

Traditional methods of removing MPs, such as filtration, coagulation, and sedimentation, face limitations in terms of efficiency and sustainability, especially for nanoscale particles.28,29 Filtration becomes energy-intensive when extremely fine pores are required and often suffers from clogging.29,30 Similarly, Zhang et al.31 demonstrated that coagulation and sedimentation techniques are usually insufficient for the complete removal of both micro- and nanoplastics. Moreover, many conventional filtration materials are non-renewable, non-biodegradable, and relatively expensive, raising concerns over their long-term environmental impact.28,32 As a result, biopolymers and NC have emerged as promising, eco-friendly alternatives due to their renewability, biodegradability, high surface area, and ease of functionalization.33–35 These materials, sourced from plant cellulose and crustacean chitosan, can be tailored for effective MP adsorption while minimizing their ecological footprint.33,34,36–40 Furthermore, the biodegradability of NC is critical for its application in removing MPs, as it ensures that the material itself will not persist in the environment or generate secondary pollution after use. This attribute strengthens its role as a genuinely sustainable, high-performing option for long-term water purification technologies.

Given the urgent need for clean water and a sustainable environment, there is increasing research interest in developing renewable membrane materials for pollutant removal. However, despite numerous studies on MP removal, comprehensive evaluations explicitly linking NC and biopolymer-based adsorbents to practical wastewater treatment performance remain limited. Existing reviews often focus narrowly on material synthesis or laboratory-scale performance without addressing integration challenges, cost-effectiveness, or regulatory considerations. Moreover, recent trends—including the push for sustainable textile processing, tightening environmental regulations, and advances in bio-based nanomaterials—underscore the urgent need for a critical synthesis of current knowledge. This review consolidates and critically evaluates recent advances in NC- and biopolymer-based systems for MP removal from wastewater, focusing on adsorption, filtration, and flocculation mechanisms. It links material performance to practical considerations for integrating wastewater treatment and achieving cost-effectiveness. It situates these findings within emerging regulatory and policy contexts to provide insights that guide future research and sustainable implementation strategies.

1.1 Source of the MPs

According to Babaei et al.,41 MPs in water come from numerous sources, which can be classified into primary and secondary categories. Understanading these sources is essential for formulating effective mitigation strategies. To visualize these origins, the primary and secondary MP pathways are depicted in Fig. 2.42 This study also illustrated that various sources voluntarily produce primary MPs, which typically measure less than 5 mm in size. Familiar primary sources include microbeads found in personal care products such as toothpaste, exfoliating scrubs, and several cosmetics. During use, these microbeads are rinsed down the drain and eventually end up in the water. Plastic pellets, commonly referred to as nurdles, serve as essential raw materials in plastics manufacturing. However, nurdles unintentionally leave the environment during handling processes or transportation.43–45 Another major contributor is the use of synthetic fibers and textiles, as their production, usage, and disposal result in considerable microfiber emissions into the environment.46 Microfibers are notably released from garments during washing due to wear and tear, as shown in a study by Parbhakaran et al.,47 which tested polyester and nylon fabrics using brush-washing methods. In contrast, secondary MPs are formed when larger plastic materials degrade into smaller pieces due to environmental factors, including weathering, UV radiation, and physical abrasion.41,47 The degradation of plastic waste, such as bottles, bags, and packaging materials, occurs through exposure to wind, sunlight, and wave action.48,49
image file: d5su00634a-f2.tif
Fig. 2 Sources and pathways of MP formation. Primary MPs come directly from products like personal care items, textiles, tires, paints, laundry, and plastic manufacturing. Secondary MPs result from fragmentation of larger plastics such as bottles, bags, fishing nets, and shipping waste. Published under the CC-BY License.42 Copyright 2023, The authors. Published by Springer-Verlag GmbH Germany.

In the field of agriculture, plastic mulches degrade over time, releasing MPs into the soil, and animals may ingest these particles when they graze on crop residues mixed with plastic mulch remnants.48,50 WWTPs can eliminate a considerable amount of MPs, but they remain a significant source of discharge. MPs originating from sources like domestic laundry and industrial wastewater can both enter and exit these facilities, ultimately reaching receiving waters.46,51,52 Urban runoff, via stormwater, transports MPs from polluted soil into aquatic environments,53 while atmospheric deposition also contaminates urban water systems.54 Moreover, abrasion of road markings and tire wear generate plastic particles, making them contributors to MP pollution.46,55

Table 1 summarizes the composition, physical form, and size ranges of MPs from various domestic, industrial, and environmental sources, providing context to their diversity and scale. Particular examples and geographical factors further emphasize the matter: in the Han River, China, the presence of MPs varied from 2315 ± 603 to 8406 ± 2055 n m−3, indicating a rising trend throughout the river.56 Research conducted in textile industrial regions has revealed elevated levels of MPs, predominantly consisting of polyester as the primary polymer type.57 Tsang et al.58 illustrated that in Hong Kong, the levels of particles found in marine waters ranged from 51 to 27[thin space (1/6-em)]909 particles per m3, while in sediments, they varied from 49 to 46[thin space (1/6-em)]143 particles per kg. A recent investigation conducted in Indiana rivers has highlighted notable MP contamination, emphasizing the extent of this problem in the Midwest's flowing waters.59

Table 1 Comprehensive overview of MP sources, their polymer compositions, physical morphologies, and size distributions
Source Composition Physical form Size range Ref.
Facial cleaners Polyethylene Spherical Higher than 0.5 mm 60
Beverage products Polyamide, acrylonitrile–butadiene–styrene, poly(ester-amide), poly(ethylene terephthalate) Fibres, fragments 0.1–3 mm 61
Textile factory Polyester Fibres 0.1–1 mm 62
Plastic mulch Polyester, polypropylene Fibres, fragments, foam, films Higher than 500 µm 63
Mariculture activities Polyester, polypropylene, polyethylene, polyamide (nylon), polystyrene, polyetherurethane, polybutylene terephthalate Fragments, flakes, fibres, foam Less than 0.25 mm 64
Anthropogenic activity Polystyrene, polyethylene, polypropylene Fibres, styrofoam, fragments, films, pellets Less than 0.5 mm 65
Urban sewage Polyethylene, polystyrene, polypropylene Fragments, lines, foam, films 1–4.75 mm 66
Construction, fishery activities, and human domestic sewage Polyvinylchloride, polyethylene, polyamide Fibres, pellets, films, fragments Less than 0.5 mm 67
Industrial area Polyethylene, polypropylene, nylon Fibres, fragments 0.1–5 mm 68
Tertiary industry Polyethylene, polypropylene, polyacrylonitrile, polyethylene terephthalate Fragments, fibers, films 500 µm to 5 mm 69
Artificial ecosystems Polyethylene, rayon, polypropylene Fibres, flakes, films, granules Less than 1 mm 70
Plastic industries Polypropylene, polyester, nylon, polystyrene Fibres, lines, spherules, fragments/granules, films Less than 0.5 mm 71
Shower gels Polyethylene Irregular shapes 422 ± 185 µm 72
Car tires Polypropylene, acrylic, nylon, rubber Fragments, fibres Higher than 500 µm 73
Facial scrubs Polyethylene, polyvinyl chloride Spherical, irregular, granular 85 to 186 µm 74
Cosmetic products Polyethylene Irregular, granular, spherical 54–115 µm 75
Industrial sources Polyethylene, nylon, polypropylene Films, fragments, lines, granules, sheets, lines 0.5–1.0 mm 76
Fishing and shipping activities Ionomer surlyn, acrylic (acryl fibre), polyetherimide, polyphenylene sulphide, ethylene vinyl alcohol, acrylonitrile, nylon, polyisoprene, polyvinyl chloride, ethylene–vinyl acetate, polyurethane Fibres, pellets, fragments 1489 ± 1017 µm 77
Personal care products, facial cleansers, sewage sludge Polystyrene, polyester, amino thermoset plastic, polyallyl diglycol carbonate Fragments, pellets, foam, films, lines 0.355–0.999 mm 78
Urbanization Polyethylene, polypropylene Pellets, fragments, films, lines, foam 0.3–4.75 mm 79
Sludge and WWTPs Polyamide, polyethylene, polypropylene Fragments, fibres, films, granules 0.003–0.05 mm 80
Local inputs, ocean transport Polypropylene, polyester, polyester, polyethylene Fibres, flakes, films, granules 2.0–2.5 mm 81
Domestic, agriculture effluent, industry, upstream inflow, and airborne settlement Polyethylene terephthalate, polyethylene, polypropylene, polystyrene, polycarbonate, polyvinyl chloride, cellulose propionate, polyamide, ethylene–vinyl acetate copolymer Pellets, fragments 0.05–5 mm 82
Commercial fish species Polyethylene terephthalate, polyethylene, polypropylene, polyamide, phthalocyanine Fibres, fragments Higher than 215 µm 83


1.2 Impact of MPs on the ecosystem

The ecological impacts of MP pollution are varied and influence organisms at various trophic levels. A wide range of aquatic organisms, extending from plankton to fish, can ingest MPs, resulting in both chemical and physical toxicity.84Fig. 3 shows the transfer of MPs through different trophic levels.85 In addition to the absorption of harmful substances that build up on the surface of MPs, ingestion of MPs may end in physical injury, such as blockages in the digestive tract.86 It can also disrupt food chains by accumulating within organisms, which leads to higher levels that can affect how ecosystems work and are structured.87,88 A study by Moto et al.89 illustrated that MPs have the potential to change habitats, disturb ecological equilibrium, and pollute water and soil. Sing et al.90 indicate that MPs have negative impacts on plant development, soil pollution, and the contamination of subsurface aquifers. The ability of MPs to absorb and interact with organic pollutants can change their toxic effects and complicate treatment efforts.91 The appearance of MPs may facilitate the movement and colonization of particular microbes, resulting in disruptions within the affected ecosystems.92
image file: d5su00634a-f3.tif
Fig. 3 MP transfer across trophic levels in the aquatic food chain (created with MS PowerPoint).

1.3 MPs in drinking water

MPs have been found in both tap and bottled water, emphasizing widespread contamination.93,94 The source of MPs in drinking water can vary, including unfiltered water sources, packaging materials, treatment processes, and distribution systems, as depicted in Fig. 4.94,95 A study by Semmouri et al.96 found the presence of MPs in surface water, ground water, and treated sewage water that serve as sources of drinking water. Another study conducted by Zhou et al.97 indicated that the amount of MPs released from plastic cups was around 556.80 ± 31.39 particles/L. In village areas, MPs can contaminate drinking water systems from purification plants and reservoirs. According to Meshram and Mhatre,98 these particles can pass through the intestinal membrane and aggregate in tissues. They have the potential to promote inflammatory responses and oxidative stress within the body.99,100 Sharma et al.100 discovered that MPs can interfere with typical composition and functioning of the intestinal microbiota, which plays a crucial role in immune and digestion response.
image file: d5su00634a-f4.tif
Fig. 4 Schematic representation of human MP exposure through the use of disposable plastic drinking cups. Published under the CC-BY License.95 Copyright 2024, The authors. Published by MDPI.

To further illustrate these impacts, Table 2 summarizes recent findings on MP sizes, affected organisms, and their observed toxicological effects. Also, they can be found in sources of drinking water, presenting a significant risk to aquatic ecosystems.84 Aquatic organisms have the ability to consume MPs, which can result in stunted growth, reduced feeding efficiency, and reproductive toxicity.101,102 MPs may also function as carriers for harmful chemicals, leading to biomagnification and bioaccumulation within the food chain 101. This trophic transfer and its cascading ecological consequences are illustrated in Fig. 5, which outlines the movement of MPs through various food web levels.103

Table 2 Summary of MP particle size, affected organisms, and reported biological effects
Origin MP exposure/size Effects Ref.
Emys orbicularis 500–1000 mg kg−1 Induced pathological changes in liver and kidney tissues 104
Ascidian ciona intestinalis 1 µm Impaired food uptake efficiency and reduced growth rate 105
Nematode 1 µm Triggered oxidative stress and induced intestinal injury 106
Crepidula onyx 2 µm Growth reduction 107
Sardinellagibbose 1 µm Decreased body weight and altered feeding behavior 108
Dania rerio 70 µm Disrupted normal gut structure 109



image file: d5su00634a-f5.tif
Fig. 5 Transfer routes of MPs from water, soil, and biota to the human body. Published under the CC-BY License.110 Copyright 2024, The authors. Published by Springer Nature Switzerland AG.

In addition, nanoplastics, due to their small size (<1 µm), show unique toxicological characteristics and pose risks distinct from those of MPs. They can translocate across biological barriers and accumulate in vital organs, potentially leading to inflammatory responses, oxidative stress, and genotoxicity.111 Moreover, they can interact with cells at the molecular level, affecting gene expression, signaling pathways, and cellular functions.112 A research conducted by Christopher et al.113 found that nanoplastics have been detected in human placentas, indicating maternal exposure and negative effects on early-life development. Exposure routes include inhalation, dermal contact, and ingestion.114 They can also accumulate biota, leading to histological damage, neurotoxicity, and metabolic disruption in fish. Additionally, they can impact soil function and food-chain transfer.115

2. MP detection

The identification of MPs in wastewater involves a series of steps that include sampling, pre-treatment, and separation, followed by identification and quantification. Many methods, such as Fourier-transform infrared spectroscopy (FTIR), pyrolysis-gas chromatography/mass spectroscopy (Py-GC/MS), and Raman spectroscopy, are used to find and measure MPs in the environment.116–118 A comprehensive overview of these MP detection techniques, including their analytical capabilities, advantages and limitations, as well as the types of polymers identified in biotic and aquatic environments, is presented in Table 3.
Table 3 Comparative evaluation of MP detection techniques, highlighting their analytical strengths and limitations, sample origins and types, measurable size ranges, and polymers identified in environmental and biological matricesa
Detection methods Advantages Limitations Source and sample type Size ranges Identified polymers Ref.
a Abbreviations: ABS: acrylonitrile butadiene styrene; ALK: alkyd resin; CPH: cellphone; EPM: ethylene–propylene rubber; EP: epoxy resin; EVOH: ethylene vinyl alcohol copolymer; LLDP/Oct: linear low-density polyethylene–octene copolymer; NY: nylon; PA: polyamide; PAN: polyacrylonitrile; PAS: polyacrylate-stryrene; PCL: polycaprolactone; PE: polyethylene; PEA: polyethylacrylate; PET: polyethylene terephthalate; PEVA: polyethylene-vinyl acetate; PMMA: polymethyl methacrylate; PP: polypropylene; PR: phenoxy resin; PS: polystyrene; PES: polyester; PTFE: polytetrafluoroethylene; PU: polyurethane; PVC: polyvinyl chloride; PVA: polyvinyl alcohol; PVAC: polyvinyl acetate; PVS: polyvinyl sulfate; RY: rayon; SAN: styrene–acrylonitrile; SBR: styrene–butadiene rubber; SR: synthetic rubber.
Optical microscopy (MO) and Fourier transform infrared spectroscopy (FTIR) • Optical microscopy assists in preliminary sorting and size classification, while FTIR provides chemical identification119,120 • Still labor-intensive and time-consuming due to manual sorting and FTIR analysis steps120 Indian white shrimps 0.157–2.785 mm PA, PES, PE, PP 121
• Combining methods reduces error rates compared to optical microscopy alone119 • FTIR spatial resolution limits detection of smaller particles, and visual sorting may miss small or transparent MPs119 Deep-sea fish <1 mm CPH, PA, PET 122
• Requires expertise and is prone to subjective bias during visual pre-sorting120 Bivalve (oyster, mussel, manila clam and scallop) 0.1–0.2 mm PE, PP, PS, PES, PEVA, PET, PU 123
Different fish species 0.2–5 mm PE, PP 124
Thamnaconus septentrional 0.04–5 mm CPH, PET, PES 125
Mussels (Mytilus edulis) 0.033–4.7 mm CPH, PET, PES 126
Benthic organisms 0.05–5 mm PP, PE, PS, PET, NY 127
Deep benthic invertebrates 0.023–6.25 mm ALK, PES 128
Different fish species 0.656 mm PS, PE, PP 129
Benthic and pelagic fish 0.217–4.81 mm PP, PE, ALK, RY, PES, NY 130
Pelagic and demersal fish 0.13–14.3 mm PA, cellulose, RY 131
Whales 0.3–7 mm RY, PES, acrylic, PP, PE 132
Atlantic herring, sprat, common dab, and whiting 0.300–0.400 mm PMMA 133
Plastic bottled water 6.5–>100 µm PET, PP 80
Glass bottled water >100 µm PA, PE, PP 80
Cardboard bottled water >100 µm Cellulose, PE, PP 80
Fourier transform infrared spectroscopy (FTIR) • Widely used and well-established technique with extensive reference databases134 • Cannot identify MPs smaller than about 20 µm (ref. 119) Ground drinking water 50–150 µm PE, PA, PES, PVC 135
• Difficult to analyze opaque and black MPs134 Tap water 100–5000 µm 136
Plastic bottled water 6.5–>100 µm PP 138
Glass bottled water 6.5–>100 µm 138
Optical microscopy (MO) and Raman microspectroscopy (RMS) • MO provides rapid visual identification and preliminary sorting based on size, shape, and color; RMS offers detailed chemical characterization and polymer identification • Both methods can be affected by MP heterogeneity and environmental aging European anchovies 0.124–0.438 mm PE 139
Bivalves (Mytilus edulis and Crassostrea gigas) >0.005 mm 140
Mussels (Mytilus edulis) and lugworms (Arenicola marina) 0.015–1 mm 141
Glass bottled water <5 µm PE, SBR 142
Plastic bottled water <5 µm PE 142
Optical microscopy (MO) • Convenient and economical method • Accuracy is relatively low; error rates of 20–70% for transparent MPs Dogfish, hake, red mullet 0.38–3.1 mm 143
• Simple operation and low cost • Time consuming and laborious Semi-pelagic fish 0.5 mm 144
• Can identify MPs with particle sizes of hundreds of microns and above119 • Cannot provide chemical composition information119
Pyrolysis-gas chromatography-mass spectrometry (pyrolysis-GC-MS) • Capable of analyzing non-volatile macromolecules by breaking them into volatile fragments for identification • Sample is decomposed during analysis Ground drinking water PE 145
• Provides detailed chemical characterization of polymers and additives in MPs • Requires specialized instrumentation and expertise
• Useful for complex samples where other methods may fail146 • Does not provide physical information such as particle size, shape, or morphology directly146
Fourier transform infrared spectroscopy (FTIR) & micro-Raman imaging microscopy • FTIR for larger particles and Raman for smaller particles and detailed chemical imaging.134 • High cost and complexity due to combining two sophisticated instruments134 Treated water from water treatment plants 1–10 µm PET, PP, PE 147
• Enhances detection accuracy and chemical identification of MPs across a wide size range119,134
• Automated or semi-automated systems can reduce analysis time and human bias148


The initial phase involves sampling, an essential procedure focused on gathering samples from WWTPs. The accuracy of this phase depends on the type of water, including freshwater, seawater, or wastewater, since timing is crucial to account for temporal and spatial fluctuations in MP levels.149 Sampling techniques can be customized according to the type of water-be it freshwater, seawater, or wastewater-because of the variations in particulate load and composition.150

After sampling, separation and pretreatment steps are carried out to separate the sample from the wastewater matrices. Filtration stands out as the most prevalent method for separation, generally utilizing filters with stainless steel basket filters that employ smaller and smaller mesh sizes (such as 10 µm, 50 µm, and 100 µm), which are effective at capturing different particle sizes.151 The process becomes better through density separation, which requires the differences in density between MPs and other particulate matter. Researchers used high-density salt solutions to enable the plastics to float, while the heavier materials settle.152 Digestion steps eliminate organic matter that could obstruct spectroscopic identification. Agents for chemical digestion, such as HCl, H2O2, and various enzymes, are applied to break down organic components while preserving the structural integrity of plastic particles.149,152 The identification of MPs is primarily carried out using spectroscopic and thermal analytical techniques. FTIR spectroscopy determines the chemical composition of MPs through the analysis of infrared absorption patterns. Using micro-FTIR along with imaging allows for a close-up and detailed study of individual particles.116,150,153 Raman spectroscopy, a widely used technique, provides information at the molecular level by analyzing rotational and vibrational modes. More advanced methods, such as Surface Enhanced Raman Spectroscopy (SERS), drastically improve detection sensitivity.153–155 Pyrolysis-GC/MS, functioning as a thermoanalytical method, thermally breaks down MPs into smaller molecular fragments for subsequent identification and separation, which is particularly useful for complex or mixed samples where direct spectroscopic identification is difficult.109,155.

Methods of quantification involve both chemical and visual tactics. Optical microscopy is often employed for quantifying microplastic particles, whereas scanning electron microscopy offers a thorough morphological understanding.149,152,153 Research into the topic of spectroscopic quantification continues, utilizing FTIR and Raman spectral data to determine the mass of MPs, although this area is still under development.156 Pyrolysis-GC/MS provides a more detailed characterization of specific polymers by determining the prevalence of their distinct degradation products.157 Innovative detection methods are consistently improving the precision and effectiveness of MP detection. Micro-flow imaging (MFI) assists in the real-time determination of MPs in situ.158 Hyperspectral imaging uses near-infrared technology and FTIR to provide very detailed images, and when combined with chemometric modeling, it helps quickly and accurately identify different types of plastics.152,159 Xue et al.154 demonstrated that new methods, such as the extreme learning machine paired with differential Raman spectroscopy, combine advanced computer learning with light detection, leading to enhanced sensitivity for biological samples. Furthermore, nanoparticle tracking analysis has been used to measure the number of nanoplastics present and their size, in response to growing concerns about plastic particles that are smaller than one micron.119 A study by Reineccius et al.120 illustrated the MP detection workflow shown in Fig. 6, highlighting key steps such as sampling using multi-corers or plankton nets, freeze-drying and digestion with hydrogen peroxide and acetic acid, separation through syringe cascades and detergent desorption, followed by detailed analysis via Raman spectroscopy.


image file: d5su00634a-f6.tif
Fig. 6 Workflow for MP detection: (1) sampling via multi-corers or plankton nets; (2) freeze-drying and digestion with H2O2 and acetic acid; (3) separation using syringe cascade and detergent desorption; (4) analysis by Raman spectroscopy. Published under the CC-BY License.120 Copyright 2021, The authors. Published by Elsevier B.V.

3. NC

NC, the most abundant biopolymer on the planet, is an excellent substrate for the massive production of affordable, ecologically sound water treatment media.121 Based on the origin of raw materials, the synthesis method, and the morphological structure, there are multiple kinds of NC materials. A variety of names have been given to these NC materials, such as nanocrystalline cellulose (NCC), cellulose nanocrystals (CNCs), cellulose nanofibrils (CNFs), cellulose microfibers (CMFs), cellulose nanofibers, nanofibrillated cellulose (NFC), microfibrillated cellulose, and various combinations of the aforementioned types.122 Each type possesses an identical chemical composition, but due to disparities in sources and extraction techniques, they differ in structure, particle size, crystallinity, and other characteristics.123Table 4 provides a comparative overview of these NC types, highlighting their synthesis methods, surface modifications, mechanical properties, recyclability, and MP removal efficiencies.
Table 4 Overview of various cellulose-based nanomaterials used for MP removal, detailing their source, size, surface characteristics, synthesis methods, mechanical properties, removal efficiency, recyclability, and application performance
Type Source Size (nm) Surface area (m2 kg−1) Synthesis method Surface chemistry/modification Mechanical properties Removal efficiency (%) Recyclability/stability Application Ref.
NCC Wood pulp, cotton, BC Width: 2–5; length: 100–300 150–250 Acid hydrolysis (typically H2SO4), enzymatic pretreatment Sulfate groups from acid hydrolysis, PEI coating, carboxylation Rigid rod-like crystals >98% removal of MPs within 20 min of adsorption Used in membranes, composites for rapid adsorption 144 and 146
CNCs Wood pulp, cotton, BC Width: 3–10; length: 100–300 Up to 150 Acid hydrolysis (typically H2SO4), mechanical pretreatment Sulfated groups, PEI, or polymer coatings Rigid crystalline rods >98% removal of MPs; rapid adsorption kinetics Incorporated in filtration membranes, aerogels 144 and 146
CNFs Wood, cotton, BC, Agave americana Diameter: 10–30 High Mechanical fibrillation (homogenization), enzymatic/chemical pretreatment (carboxymethylation) Sulfonation (–SO3H), carboxylation (–COOH), PEI coating Flexible, forms entangled 3D porous aerogels 88.8% removal of PS-NH2 MPs; adsorption capacity 586.95 mg g−1 >78% efficiency after 10 cycles Used in aerogels, filters 29, 144 and 145
NFC Wood pulp, agricultural residues Diameter: 10–30 High Mechanical fibrillation, chemical pretreatment (TEMPO oxidation) TEMPO-oxidized carboxyl groups Flexible, entangled fibrils Comparable to CNFs; good adsorption Good recyclability Used in filtration membranes, aerogels 144 and 145
Micro fibrillated cellulose (MFC) Bleached wood pulp Width: 5–30 Moderate to high Enzymatic or chemical pretreatment + high-pressure homogenization Moderate mechanical strength Up to 59% removal efficiency Low recyclability Used in preliminary MP removal filtration 144 and 148
CMF Various cellulose sources Diameter: 200–300 Moderate Microwave-assisted acid hydrolysis + g_C3N4 synergy (10 min) 99% removal with an attapulgite (APT) composite Moderate Composite filters for MP removal 148
Bacterial NC BC (Acetobacter xylinum) Diameter: 20–100 High Bacterial biosynthesis Typically unmodified, high purity Uniform size 144 and 148
Cellulose benzoate (modified CNCs) Cellulose esterified in an ionic liquid (AmimCl) Esterification in an ionic liquid + CNT/MCNT incorporation Modified with carbon nanotubes (CNTs), magnetic carbon nanotubes (MCNTs) >97% removal of MPS with CNT/MCNT modification Enhanced π–π interactions and zeta potential for adsorption 147
CNF-coated delignified wood (CNF-CDW) Balsa wood CNF diameter up to 10 to 20; wood pores micron scale Delignification (NaClO2, Na2SO3/NaOH, DES) + CNF coating + CaCl2 crosslinking CNF-film coating on wood; cross-linked Flux 1146 L m−2 h−1 95.97% removal of MPs Sustainable, reusable filter Combined mechanical filtration and adsorption 28


NCC—also referred to as CNCs, nanocrystals of cellulose, or cellulose nanowhiskers—is an exceptionally robust form of NC usually retrieved from cellulose fibrils by acid hydrolysis.123 The extended, malleable, and interwoven NC that can be mechanically separated from cellulose fibrils is called NFC, often referred to as cellulose nanofibrils (CNFs) or nanofibrillar cellulose.124,125 Another sort of NC is bacterial NC, which is primarily manufactured by G. xylinus and can be recovered from the ingestion of tiny molecular carbohydrates by bacteria.126 Hydrolysis with extremely potent acids yields the nanocrystalline particles by breaking local crystalline bonds between nanofibrils and rupturing amorphous domains.127 Cellulose fibers undergo mechanical breakdown into CNFs most frequently by refining, high-pressure homogenization, and grinding.125 Bacterial cellulose (BC) can be produced by Acetobacter aceti, and it can be optimized by the fermentation process.128Fig. 7 shows different types of NC materials.129–137


image file: d5su00634a-f7.tif
Fig. 7 Microscopy image of (a) CMFs. Reproduced with permission from ref. 129. Copyright 2021, Springer Nature; (b) cellulose fibers (CFs). Published under the CC-BY License.130 Copyright 2017, The authors. Hindawi; (c) cellulose nanoparticles (CNPs). Reproduced with permission from ref. 131. Copyright 2007, Elsevier Ltd.; (d) CNCs. Published under the CC-BY License.132 Copyright 2018, The authors. Published by MDPI; (e) cellulose nanofibers. Reproduced with permission from ref. 133. Copyright 2009, Royal Society of Chemistry; (f) BC and (g) cellulose nanofibers assembled into a material stronger than spider silk. Published under the CC-BY License.134 Copyright 2018, The authors. Published by American Chemical Society; (h) electrospun cellulose nanofibers. Reproduced with permission from ref. 135. Copyright 2012, Elsevier Ltd.; (i) cellulose aerogels. Published under the CC-BY License.136 Copyright 2018, The authors. Published by MDPI.

However, the synthesis of various NC materials faces several challenges primarily related to processing conditions and material properties. Traditional methods for NC preparation, such as mechanical, biological, and chemical treatments, have limitations including long treatment times, high energy consumption, and environmental concerns.138 For instance, the production of CNCs often involves acid hydrolysis, which requires careful control to avoid degrading the cellulose while removing amorphous regions.139,140 CNFs, produced via mechanical methods, can suffer from high energy consumption during fibrillation.141 BNC, although pure, requires specific culture conditions and can be costly to produce at scale.142 Modified CNCs, like cellulose benzoate, and composites like CNF-CDW require additional chemical modification steps that can introduce complexities in maintaining structural integrity and desired properties.143

3.1 NC characteristics relevant to MP removal

3.1.1 High surface area and porosity. The high specific surface area of NC is one of its outstanding characteristics, and it contributes to wastewater treatment. The adsorption capacity of materials based on NC for capturing pollutants and the size exclusion capability of eliminating undesired elements may be improved by increasing the specific surface area of NC and its interactions with the surrounding matrix.144 The adsorption of MPs is greatly dependent on the high specific surface area of the NC and the microporous structure of the NC aerogel.160 Among many other qualities, excellent mechanical properties of NC, ease of processing into porous 2D or 3D structures, and exceptionally reactive surface with high surface area (resulting in high density) make it a great building block for designing functional nanomaterials by mineralization.161 Pickering foam constructed from CNCs has a low density, which makes it possible to dry it to create porous materials with numerous pore structures and a large specific surface area. Reducing inner density is an achievable approach to improve the specific surface area of objects with known shapes and volumes.162
3.1.2 Biodegradability. NC is one of the most intriguing plant-based biodegradable biopolymers.163 Nanomaterials derived from biological sources have particular characteristics of nanomaterials along with the further benefits of sustainability, abundance, and biodegradability.33 This biodegradability arises from its composition of glucose units linked by β-1,4-glycosidic bonds, which are susceptible to enzymatic breakdown by cellulose enzymes produced by different microorganisms.164 However, the biodegradation of NC can be affected by several factors, including its source, surface modification, production process, and environmental conditions to which it is exposed.165 Environmental factors such as pH, temperature, moisture levels, and the presence of certain organisms play an important role in influencing the degradation of NC.166 When conditions are ideal, the performance of cellulose enzymes is enhanced, leading to a higher decomposition rate of NC into basic substances. Hossain et al.164 found that the degree of crosslinking in NC-based superabsorbent polymers can influence their biodegradability. Higher crosslinking density may impede enzyme accessibility, thereby delaying the degradation process. Another study conducted by Frank et al.165 demonstrated that dispersibility within polymer matrices can also impact its biodegradation. For example, research has illustrated that hydrophobic modifications via silanization can reduce the biodegradability of NC.

3.2 Mechanisms of MP removal using NC

The application of NC in MP remediation operates through several key mechanisms. Fig. 8 provides a schematic overview of four mechanisms such as adsorption, filtration, aggregation, and surface modification, each of which is elaborated below.
image file: d5su00634a-f8.tif
Fig. 8 Schematic representation of four NC-based mechanisms for MP removal (created with MS PowerPoint).
3.2.1 Adsorption. TEMPO-mediated oxidation has been identified as an exceptionally effective technique for generating cellulose nanofibers due to its selectivity and low energy consumption.167 Due to the high attraction between surfaces with opposite charges, the positively charged MPs (polystyrene) instantly bind to the anionic TEMPO-CNF surface during adsorption. Additionally, anionic MPs can more readily enter the NC network in the anionic system because the attraction energy between negatively charged surfaces is half that of surfaces with opposite charges. To boost the effectiveness of removing anionic and nonionic contaminants from NC, the hydroxyl groups can also be chemically modified.144 These adsorption studies emphasize that surface chemistry and functionalization strongly influence MP capture, providing a conceptual bridge to the membrane selectivity principles discussed in the following filtration section.
3.2.2 Filtration. NC can be used to create membrane filters that physically trap MPs.40,168 These membranes are designed with pore sizes smaller than the MPs, ensuring their retention while allowing water to pass through.168 NC-based membranes offer advantages such as low energy consumption, high separation efficiency, and eco-friendliness.40 The effectiveness of these membranes can be improved by modifying the NC to improve its stability and mechanical strength.169 For instance, the addition of sulfonated or cationic CNCs (S-CNCs and C-CNCs) to water-based drilling fluids reduces filtration volume at different temperatures, illustrating their capability in filtration applications. Fig. 9 demonstrates the filtration volume against the square root of time at various temperatures with varying concentrations of C-CNC and S-CNC.170 These findings suggest that coupling adsorption pretreatments with filtration could mitigate fouling and enhance overall MP removal, underscoring the value of integrated treatment designs.
image file: d5su00634a-f9.tif
Fig. 9 Filtration volume (V) versus square root of time (T1/2) for base mud and CNC-modified muds (C-CNC and S-CNC) at 25 °C, 150 °C, and 180 °C, demonstrating the influence of CNC concentration and temperature on fluid loss behavior. Published under the CC-BY License.170 Copyright 2024, The authors. Published by Springer Nature B.V.
3.2.3 Aggregation. NC can induce the aggregation of MPs, leading to the formation of larger particles that are easier to remove.171,172 This process can be improved through the addition of coagulants, such as aluminum and ferrous sulfate, which destabilize the MPs and promote their clumping together. For example, coagulation with aluminum and ferrous sulfates has proven effective in removing polystyrene and polyvinyl chloride MPs from natural surface water. The efficiency of MP removal can be further enhanced by optimizing the dosage of coagulants and by using NC to create a matrix that entraps the aggregated MPs.173
3.2.4 Surface modification. Pristine NC contains numerous hydroxyl groups that can be chemically modified to introduce functional groups with a high affinity for MPs.174,175 Several methods can be employed, such as chemical modification, graft copolymerization, adsorption and bioconjugation. In chemical modification, oxidation, esterification, and etherification can alter the surface properties of NC, making more effective for adsorption.176 A study by Kopač et al.177 introduced cationic groups that can increase the electrostatic attraction between NC and negatively charged MPs. Fig. 10 shows SEM micrographs of different types of cellulose-based nanofibers, including cationic CNFs, cationic microfibrillated cellulose, freeze dried cellulose nanofibers, and quaternized CNFs, illustrating their individual morphologies.177 Another technique, graft copolymerization, involves grafting polymers onto the NC surface to fine-tune its properties. By grafting specific polymers, NC can be engineered to selectively bind to different types of MPs.178 Furthermore, modifying the surface of NC through adsorption and bioconjugation can improve its functionality and biocompatibility. This can lead to better cell adhesion and controlled degradation, making it suitable for various biomedical applications.179
image file: d5su00634a-f10.tif
Fig. 10 Micrographs of different types of cellulose-based nanofibers. Published under the CC-BY License.177 Copyright 2022, The authors. Springer Nature B.V.

Several techniques are available for surface modification, each offering unique advantages depending on the application. For instance, TEMPO (2,2,6,6-tetramethylpiperidine-1-oxyl) is a stable nitroxyl radical widely used in surface modification.180 It is frequently employed to modify CNFs by introducing carboxy groups.181,182 These carboxy groups can then be further functionalized; for instance, primary-amine-terminated polyalkylene glycol (PAG) can react with carboxy groups in TEMPO-CNFs to form amide bonds, improving thermal and dimensional stability.181 Another surface modification technique is amine functionalization, which involves introducing amine groups (–NH2) onto the surface of a material.183 A common method for amine functionalization is silanization using 3-aminopropyltriethoxysilane (APTES).184,185 The ethoxy groups in APTES react with hydroxyl groups on the surface, forming stable siloxane (Si–O–Si) covalent bonds.184 Other surface modification techniques such as cationic surface functionalization using cetrimonium bromide can improve interfacial interactions between CNCs and polymeric matrices in nanocomposites.186

4. Biopolymers for MP removal

Biopolymers are gaining increasing attention as sustainable materials for several applications, including MP removal from wastewater. These polymers offer eco-friendly alternatives to traditional synthetic polymers due to their renewability and biodegradability. Various types of biopolymers have shown promise in MP removal, as shown in Fig. 11 and detailed in Table 5.
image file: d5su00634a-f11.tif
Fig. 11 Different types of biopolymers for MP removal (created with MS PowerPoint).
Table 5 Comparative evaluation of biopolymers based on source, functional groups, MP removal efficiency, and underlying mechanisms
Biopolymer Source Functional groups MP removal efficiency Mechanism Ref.
Chitosan Derived from chitin in crustaceans (shrimp, crab), fungi, insects –NH2, –OH (primary hydroxyl groups at the C-6 position and secondary hydroxyl groups at the C-3 position) >90% (depends on pH, dosage, type of MP) Electrostatic attraction (between cationic amino groups and anionic MPs), H-bonding, van der Waals; enhanced by grafting/cross-linking 187–189
Alginate Brown seaweed (phaeophyceae), bacteria –COOH, –OH 62–99.79% Flocculation, electrostatic interaction, hetero-aggregation, physical encapsulation in a Ca-alginate matrix 190–193
Starch Corn, potato, wheat, cassava –OH, N+(CH3)3 (cationic modified) Up to 90% with additives Charge neutralization, bridging, flocculation, physical entrapment; performance influenced by particle density & age 194–197
Polysaccharides Plants, algae, animals (e.g., laminarin, starch, alginate, chitosan) –COOH, –OH, –NH2 93–99% (e.g., laminarin gels) H-bonding, sweeping/entrapment, bridging, van der Waals, electrostatic interactions 195, 197 and 198
Lignin Wood, pine bark, Miscanthus, paper industry byproduct –OH (phenolic/aliphatic), –COOH, OCH3 Raw: up to 26%; modified: up to 99% π–π stacking, hydrophobic interaction, H-bonding, electrostatic, flocculation (hydrogels, Fe-biochar), magnetic separation 199–202
Pectin Citrus fruits, apples –COOH, –OH 93–99% (gel systems with coagulants) H-bonding, sweeping/entrapment, bridging, van der Waals, coagulation & flocculation 198 and 203
Xanthan gum Fermentation by Xanthomonas campestris –OH, –COOH, acetyl groups >90% (coagulant blends) H-bonding, electrostatic interactions, bridging, gel floc entrapment; can be enhanced via chemical modification 204, 205 and 197
Carrageenan Red algae (e.g., Kappaphycus, Gigartina) –OSO3 (sulfate), –OH, –OCH3 >90% (gels and hydrogels) Physical entrapment in the gel matrix, electrostatic attraction (sulfated groups), H-bonding 206 and 207
Cyclodextrins Enzymatic conversion of starch (corn, potato) –OH (primary and secondary), hydrophobic cavity >80–90% (for organics) Host–guest inclusion, H-bonding, van der Waals; enhanced when in composites for aggregation/flocculation 208 and 209


4.1 Chitin and chitosan

Chitosan, a naturally derived biopolymer, is a modified form of chitin.210 It is the most abundant natural polysaccharide found in the exoskeletons of crustaceans (crab, shrimp, and lobster), insects, and fungal cell walls.211,212 The deacetylation of chitin yields chitosan.211,213,214 The structure of chitosan features amino and hydroxyl groups, as depicted in Fig. 12, which play an important role in its ability to interact with pollutants.214,215 The amino groups on the structure of chitosan become positively charged under acidic conditions, facilitating electrostatic interactions with negatively charged MPs.213 This leads to flocculation and coagulation, where small MPs aggregate into larger flocs that can be easily separated from the water.216 The porous structure and reactive functional groups of chitosan enable it to adsorb MPs, effectively trapping them within its matrix.217 Its effectiveness in MP removal stems from its ability to act as an adsorbent and bioflocculant.34,216 As a bioflocculant, chitosan promotes the aggregation of MPs, leading to their sedimentation or easier removal through filtration.216,218 Additionally, shaping chitosan into beds increases its surface area and makes it easier to handle and regenerate.212 Nano-sized chitosan exhibits a high surface area and improved adsorption capacity, and higher MP removal efficiency.219
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Fig. 12 Derivation of chitosan via chitin deacetylation (created with MS PowerPoint).

4.2 Alginate

Alginate, a naturally occurring biopolymer extracted from brown algae,220 is a developing sustainable and efficient solution for MP removal from wastewater.220,221 Its biocompatible, cost-effective, and nontoxic features make it suitable for various applications.222 It is a linear polysaccharide composed of two uronic acid monomers, guluronic acid and mannuronic acid.223 The ability of alginate to form gels in the presence of divalent cations, such as calcium ions, is a key property utilized in MP removal.224 Zhang et al.221 showed that calcium alginate hydrogel can be used as a flocculant to remove MPs from water, with a removal efficiency of up to 99.5% for certain MPs. Although the effectiveness of this method can vary depending on the composition and size of the MPs. For more effective removal, Wang et al.222 demonstrated that alginate can be combined with other materials to form composites with enhanced adsorption capabilities. Additionally, alginate can be used to entrap other materials, such as nano-zerovalent iron, to degrade organic pollutants through advanced oxidation processes.225 The functional groups present in alginate can also interact with the surface of MPs, enhancing their removal.152 It can be processed into various useable forms, such as beads or membranes, making it versatile for water treatment technologies.226Fig. 13 illustrates the molecular structure of alginate.227
image file: d5su00634a-f13.tif
Fig. 13 Structural composition of alginate (created with MS PowerPoint).

4.3 Starch

Starch is an emerging biopolymer for MP removal from wastewater due to its availability, biodegradability, and low cost.228,229 Modified and unmodified forms of starch are being explored for their ability to capture and remove MPs through various mechanisms, offering an environmentally friendly alternative to traditional methods.194 Gao et al.194 illustrated that cationic-modified starch (CS) is efficient as a bio-coagulant for removing MPs of different sizes, types, and aging conditions under different water conditions. Additionally, starch can destabilize MP suspensions, causing them to aggregate and form larger flocs that can be easily removed.194,230 Another research conducted by Amin et al.231 combined clay and cationic starch to enhance biodegradability and cost-effectiveness. Furthermore, ultralight porous sponges made from crosslinking corn starch and gelatin have been developed for capturing micro- and nano-scale plastics, with the added benefit of being enzymatically decomposable to glucose.232Fig. 14 demonstrated that the primary chemical framework of starch-based polymer.233
image file: d5su00634a-f14.tif
Fig. 14 Fundamental molecular structure of starch polymer (created with MS PowerPoint).

4.4 Polylactic acid

Polylactic acid (PLA) is an attractive alternative to conventional petroleum-based polymers because of its biocompatibility, biodegradability, and renewability.234–236 It can be processed using techniques like extrusion, injection molding, and electrospinning.237,238 This versatility allows for the creation of various membrane structures and forms suitable for different filtration and adsorption methods in MP removal from wastewater, as shown in Fig. 15.239 For instance, 3D printing methods can be used to create PLA membranes with controlled porosity and dimensional stability.234,240 Khalil et al.241 developed asymmetric ultrafiltration membranes based on PLA for the removal of MPs from wastewater. These membranes, characterized by techniques such as FTIR, XRD, SEM, and porosity analysis, have shown high removal efficiencies for organic matter. Furthermore, advanced PLA-based membranes embedded with functionalized nanomaterials, such as positively charged multi-walled carbon nanotubes/graphene oxide (f-MWCNTs/GO) nanohybrids, have been developed to enhance water flux and nutrient removal. For example, the addition of only 1.5% f-MWCNTs/GO nanohybrid into the PLA matrix increased water flux by 74% compared to unmodified membranes and achieved removal rates up to 90.1% for ammonium nitrogen and 71.3% for phosphate ions from raw wastewater.242
image file: d5su00634a-f15.tif
Fig. 15 Chemical structure of polylactic acid (PLA) (created with MS PowerPoint).

4.5 Polysaccharides

Polysaccharides can act as bioflocculants, aggregating MPs into larger, settleable flocs. For instance, an extracellular polymeric substance produced by a freshwater Cyanothece sp. strain demonstrated bioflocculant capacity when exposed to micro- and nano-plastics.243 Jagadeesh and Sundaram244 found that modified polysaccharides can absorb MPs onto their surface, facilitating their removal. Furthermore, organosilanes combined with polysaccharides can be used to agglomerate and fix MPs, enabling their removal from water.245 Biochar, which can be derived from polysaccharide-rich biomass, has shown potential for MP removal through mechanisms such as “Stuck,” “Trapped,” and “Entangled” interactions. However, hybrid biochar-sand filters have shown promise as low-cost systems.246 The chemical structure of polysaccharide chains is shown in Fig. 16. Furthermore, acrylamide (AM) cross-linked psyllium polysaccharide (PLP-AM) has been synthesized and used as a flocculant for removing PS, PVC, and PET MPs from water. Under optimal conditions, PLP-AM achieved removal percentages of 92.55% for PS, 93.85% for PET, and 94.31% for PVC.247 Polysaccharides can be extracted from spirulina platensis using hot water, followed by chitosan flocculation treatment to remove impurities.248,249
image file: d5su00634a-f16.tif
Fig. 16 Polymeric structure of polysaccharides (created with MS PowerPoint).

4.6 Lignin

The complex structure and abundant functional groups of lignin make it a viable option for adsorbing pollutants, including MPs, from wastewater.250,251 Studies have explored the direct application of lignin as an absorbent for MPs. For example, organosolv lignin derived from Miscanthus sp., pine bark, and solid anaerobic digestates has been evaluated as an adsorbent for various types of MPs.199 Additionally, lignin-based materials, especially when processed into activated carbons or porous structures, offer a high surface area and porosity.252,253 MPs can become entrapped within these pores through physical adsorption.253 Cationic lignin polymers can neutralize the negative surface charges commonly found on MPs in wastewater.254 This charge neutralization reduces repulsive forces between MP particles, allowing them to aggregate.255 Furthermore, lignin polymers can act as bridges between MP particles, linking them together to form larger flocs.254 These larger flocs are then easier to remove via sedimentation or filtration.256,257 Kaur et al.258 demonstrated that lignin can degrade MPs under light irradiation. Lignin can be chemically modified with [2-(methacryloyloxy)ethyl]trimethylammonium chloride (METAC) or acrylic acid to improve its charge density, water solubility, and molecular weight, improving its flocculation performance.254,255,259 For example, introducing cationic groups through METAC can enhance the ability of lignin to flocculate negatively charged MPs.255 The underlying polymeric structure of lignin is demonstrated in Fig. 17.
image file: d5su00634a-f17.tif
Fig. 17 Chemical structure of lignin (created with MS PowerPoint).

5. Coagulation and flocculation mechanisms

Coagulation and flocculation are crucial processes for removing MPs from wastewater.260 These processes involve destabilizing suspended particles, including MPs, and aggregating them into larger flocs that can be easily removed through sedimentation or filtration.261,262 Coagulation involves neutralizing the surface charge of the suspended particles, allowing them to aggregate.262,263 Common coagulants such as aluminum-based salts (such as alum) and iron-based salts (such as ferric chloride) destabilize the MPs by reducing the repulsive forces between them, promoting initial aggregation.264,265 Flocculation, on the other hand, involves the addition of polymers that bridge the destabilized particles, forming larger, more settleable flocs.262,266 These polymers, often polyacrylamides, improve the aggregation of MPs, leading to improved removal efficiency.267 A research by Awan et al.268 illustrated that high dosages of coagulants can lead to the formation of a precipitate that enmeshes MPs, facilitating their removal. This is often referred to as sweep flocculation. Fig. 18 presents the coagulation–flocculation strategy for MP elimination.269 Flocculation thus complements both adsorption and filtration methods, indicating that multi-stage or hybrid systems may provide the most scalable and sustainable solutions.
image file: d5su00634a-f18.tif
Fig. 18 Schematic overview of coagulation–flocculation in MP treatment. Reproduced with permission from ref. 269. Copyright 2024, Institution of Chemical Engineers. Published by Elsevier Ltd.

However, pH affects the surface charge of MPs and the speciation of the coagulants used in flocculation.270 A research conducted by Ummalyma et al.271 have shown that the surface charge of algal cells changes with pH, which affects flocculation efficiency. For instance, maximum flocculation efficiency (94%) was achieved by changing the medium pH from 8.5 to 12 through addition of NaOH. Similarly, in Yellow River water treatment, the pH influences the coagulation behavior and floc properties when using ferric-based coagulants. The pH also affects the structure of humic acid flocs, where flocs formed at pH 5 with low coagulant dosage exhibited a compact structure and high strength.272 Ionic strength also influences the electrostatic interactions between MPs and flocculants by affecting the electrical double layer surrounding the particles.273 Higher ionic strength can compress the double layer, reducing the repulsive forces between particles and promoting aggregation.274 However, excessive ionic strength can lead to destabilization of the suspension and hinder flocculation.275 Studies have shown that increasing ionic strength accelerates aggregation.274 In a similar way, the ionic strength affects floc formation and growth in polymer-clay flocculation.273,275 The effect of total hardness and ionic strength on coagulation performance has been investigated using titanium tetrachloride, showing that these parameters influence the removal of organic matter.276

The combined effect of pH and ionic strength determines the overall efficiency of flocculation. For instance, in aluminum sulfate-induced microalgae flocculation, changes in pH and ionic strength influence algal flocculation by altering the zeta potential of cells. This relationship is described by the classical DLVO theory, where cells with lower total DLVO interaction energy exhibit higher flocculation.270Table 6 provides a summary of coagulant and flocculant performance for MP removal, including dosage, target MP types, efficiency, and key limitations.

Table 6 Overview of treatment agents: removal efficiency and associated limitations
Coagulant/flocculant Dosage (mg L−1) MP type(s) Removal percentage Drawbacks Ref.
Alum (aluminum sulfate) 50–100 HDPE, general MPs HDPE: 86.6; PS: 67 High sludge, pH reduction 277 and 278
Ferric chloride 50–100 HDPE, PS PS: 48 Corrosive, heavy metal risk, sludge management 277 and 278
PAC 0.4 mmol L−1 PS, PP, PVC, PA, PE, PU PS: 97 Cost, residual Al, pH sensitivity 278
PAC + chitosan PET PET: up to 90; improved for others Cost, limited scale, stability issues 279
Chitosan 10–40 PET PET: up to 90 Higher cost, limited scale, pH sensitive 279
Moringa oleifera seed extract (MOCP) 100–150 HDPE, PE, pristine & weathered MPs PE, HDPE: 70–87 Variable quality, shelf life, less effective for some MPs 277, 278 and 280
Benincasa hispida extract 100 HDPE, general MPs HDPE: 83.7 277
Protein-coated sand (f-sand) PE (weathered) 60 Lower efficiency, charge reversal issues 278 and 280


6. Adsorption mechanism

Adsorption mechanisms are complex and depend on several factors, including the properties of the MPs, the adsorbent material, and surrounding environmental conditions.281–283 Different MP types have varying chemical compositions and surface properties, which can affect their affinity for pollutants like 4-nonylphenol.284 Additionally, the surface area,284 pore size,285 surface charge,286 and chemical functional groups of the adsorbent material determine its capacity to bind MPs. For example, the linear mycelium of Ganoderma lucidum shows high adsorption efficiency due to its morphology, achieving equilibrium adsorption capacities of 102.92 mg g−1 for polyethylene, 156.39 mg g−1 for polypropylene, and 311.76 mg g−1 for polystyrene.287 Narwal et al.282 showed that interactions between π electrons in aromatic rings can improve if both the MP and adsorbent have aromatic moieties. Another study by Yuan et al.288 showed that 3D RGO has adsorption capacity of polystyrene MPs, showing a distinct porous spatial structure beneficial for adsorption. As shown in Fig. 19, various physicochemical interactions contribute to the adsorption of contaminants by MPs.289
image file: d5su00634a-f19.tif
Fig. 19 Illustration of interactions involved in the adsorption of pollutants onto MP surfaces, including electrostatic forces, hydrogen bonding, hydrophobic interactions, π–π stacking, cation bridging, van der Waals forces, partitioning, and pore-filling. Published under the CC-BY License.289 Copyright 2022, The authors. Springer Nature Switzerland AG.

To understand the interaction between absorbers and absorbents, adsorption isotherm models are important. They provide a mathematical description of the adsorption process, essential for predicting the behavior of adsorption systems. The Langmuir isotherm is one of the models that assume monolayer adsorption onto a homogeneous surface with identical adsorption sites and no interaction between adsorbed molecules.290–292 The Langmuir model is expresses as:

image file: d5su00634a-t1.tif
where qe is the equilibrium adsorption capacity (mg g−1), qm is the maximum adsorption capacity (mg g−1), KL is the Langmuir adsorption constant (L mg−1), and Ce is the equilibrium concentration of the adsorbate in solution (mg L−1)

Several studies have utilized the Langmuir isotherm model for adsorption processes. For example, the adsorption of Cd and landfill leachate on wood-derived biochar was analyzed, and the Langmuir model was one of the isotherms applied.293 Similarly, the adsorption of nitrate onto solid olive mill residues was examined using the Langmuir isotherm, yielding the equation y = 0.007x + 0.4576 with R2 = 0.9787, indicating a good fit.294 In another study, the adsorption of benzene onto grass-derived biochar was modeled using the Langmuir isotherm, resulting in KL = 0.008, qm = 238.9, and R2 = 0.934.292 Another mathematical model is the Freundlich isotherm, which is an empirical model that describes adsorption on heterogeneous surfaces, where adsorption energy varies across different sites.290–292 The Freundlich model is expressed as:

qe = KFCe1/n
where qe is the equilibrium adsorption capacity (mg g−1), KF is the Freundlich adsorption constant, Ce is the equilibrium concentration of the adsorbate in solution (mg L−1), and n is the Freundlich exponent, reflecting the intensity of adsorption or surface heterogeneity.

Zand and Abyaneh293 found that the adsorption of Cd from landfill leachate and the adsorption of nitrate onto solid olive mill residues fit the experimental data with the equation y = 0.3888x + 2.5552 and R2 = 0.9816.294 The adsorption of benzene onto grass-derived biochar was also modeled using the Freundlich isotherm, resulting in parameters KF = 8.065, n = 1.778, and R2 = 0.963.292 While Langmuir and Freundlich isotherms are commonly used, other models such as the Temkin, Redlich–Peterson, Sips, Toth, Dubinin–Radushkevich, and Koble–Corrigan isotherms can also be employed to describe adsorption processes, especially when the assumptions of Langmuir and Freundlich models are not fully met.291,292,295–297

7. Synergistic application of NC and biopolymers

Biopolymers combined with NC form composite materials with enhanced properties for MP removal.298 For instance, the integration of NC and chitosan results in synergistic effects, increasing overall adsorption capacity and selectivity for MPs.299 Wu et al.300 developed a sustainable, environmentally adaptable adsorbent through the supramolecular self-assembly of chitin and cellulose. This biomass-based fibrous framework exhibited excellent adsorption performance across various MP types. Similarly, Mok et al.301 demonstrated that reusable polyvinyl alcohol/chitin/NC biopolymer composite films, crosslinked with maleic acid, effectively removed both MPs and methylene blue dye. Another renewable and abundant biopolymer, starch, when combined with NC, shows improved mechanical properties and enhanced MP capture and retention capabilities.302 Additionally, composite aerogels made from activated carbon and NC blended with cross-linked biopolymers such as hydroxypropyl methylcellulose and chitosan have been evaluated for their ethylene gas adsorption capacity, as illustrated in Fig. 20.303 Although this study focused on gas removal, the materials' high porosity and surface area suggest strong potential for MP adsorption applications as well.298 The synergistic application of NC and biopolymers is commonly used for those MPs that cannot be eliminated through the sole biopolymer or NC. Fig. 21 shows the removal efficiency of NC, biopolymer, and synergistic materials.304
image file: d5su00634a-f20.tif
Fig. 20 Aerogel structure comprises atom or nanoparticle clusters forming a solid network (green), with interstitial spaces representing its pores. Published under the CC-BY License.303 Copyright 2018, The authors. Published by MDPI.

image file: d5su00634a-f21.tif
Fig. 21 Removal efficiency comparison across NC, biopolymer, and synergistic materials (created with MS Excel).

Despite the advantages, NC and biopolymers face compatibility challenges. Many biopolymers are hydrophilic, while some NC modifications can introduce hydrophobic characteristics, leading to poor compatibility.179 Poor interfacial bonding can degrade the mechanical properties of the composite material, reducing its overall effectiveness in MP removal.305 Additionally, NC has a tendency to aggregate due to strong hydrogen bonding between individual fibers.306 Uniform dispersion on the NC matrix is important for achieving optimal functional properties.307 Incomplete dispersion can lead to stress concentration points and reduced performance of the composite material.308,309

8. Sustainability of NC and biopolymer-based treatment systems

The advancement of renewable, sustainable, biodegradable, environmentally sound, safe, and sustainable materials depends on the fabrication of NC-based products.124 NC can be created from bacteria, plants, or biomass using relatively straightforward, scalable, and effective isolation methods. The most common nanostructured component found in wood, cotton, hemp, flax, and other plant-based materials is cellulose, which is biodegradable and non-toxic. One can extract NC from renewable resources via mechanical, chemical, enzymatic, or a combination of these methods. Source, isolation method, and possible surface changes all affect the characteristics of NC.310 Ali et al.311 demonstrated that materials based on NC work well as adsorbents for pollutants in water. By enriching the surface of materials like NC, water contaminants can be eliminated. Water treatment methods, especially adsorption, are required to meet the growing demand for clean water and to mitigate pollution caused by bottled water waste. However, adopting the right adsorbent is an important issue for water treatment since it necessitates striking a careful balance between natural components, high removal effectiveness, ease of separation from treated water, environmental friendliness, and economic viability. As a result, there is a lot of interest in creating innovative adsorbent films, such as bacterial NC-clay film, for use in water treatment.312 NC is a prime contender to enable novel, sustainable, and affordable water purification technologies because of its special physicochemical characteristics, which include high surface area, several functions, nontoxic and biodegradable characteristics, and scaffolding stability and versatility.313 Academic research discussing the cutting-edge advantages of using NC-based membrane filtration processes has grown exponentially, reflecting the predicted success of NCs in the field of improving water quality through membrane filtration processes.314 This move to a bio-based solutions solve our worldwide plastic pollution problem and offers a chance for a circular economy, which would decrease reliance on fossil fuels and create a cleaner environment.315

In the case of biopolymers, the most prevalent kind of biobased polymer, polyhydroxyalkanoate (PHA), is made by a variety of microorganisms and acts as a carbon and energy storage medium.316 PHA is a viable substitute for non-biodegradable petro-based plastics due to its biodegradability and advantageous material properties.317 Prior research explored the ability of synthetic biomaterials to absorb or immobilize pollutants, as well as their adsorption capabilities for eliminating a variety of impurities and enhancing water quality.318

However, carbon footprint analysis plays a crucial role in assessing the overall environmental impact of NC and biopolymer production and application.319,320 This analysis involves quantifying greenhouse gas emissions throughout the entire life cycle, from raw material extraction to end-of-life disposal.321,322 In this context, particular attention should be given to electricity and chemical consumption, which are critical sub-aspects influencing carbon footprint growth.319 To enhance sustainability, the choice of disposal methods for NC and biopolymer-based products is also significant.323 Therefore, sustainable end-of-life management should align with circular economy principles, emphasizing the safe and economical recycling and reuse of composite plastics.324 Additionally, employing energy-efficient manufacturing processes, such as chemo- and bio-mechanical methods, can substantially reduce the energy requirements for NC production.325

Moreover, several Life Cycle Assessment (LCA) studies have compared synthetic polymers with biopolymer/NC-based materials to evaluate environmental trade-offs.148 For instance, the LCA of garbage bags made from polyethylene (PE), biomass polyethylene (Bio-PE), and poly(butylene adipate-co-terephthalate)–starch blends (PBAT/starch) illustrates the potential benefits of bioplastics in waste management scenarios.326 Supporting this, a review of LCA studies on NC-based adsorbents highlights their effectiveness in environmental remediation applications.327 Furthermore, an LCA conducted by Hervy et al.328 confirms that NC materials typically exhibit a lower environmental footprint, particularly concerning resource consumption.

9. Regulatory framework and policies

Mitigating MP contamination in emerging nations requires an understanding of the laws and policies governing plastic waste in the coastal environment.329 Many countries implemented laws and regulations to reduce plastic pollution or are in the process of engaging in stakeholder discussions, as demonstrated in Table 7. These laws and regulations differ in their approach (i.e., traditional viewpoint (top-down) methods, market-oriented approaches, and voluntary efforts) because African nations have different customs for the consumption, manufacture, and disposal of plastics.330 Aquatic systems were mostly exposed to MPs from WWTPs. However, a sustainable governance framework—such as the one proposed by the European Parliament in its review of the Urban Waste Water Treatment Directive (TA/2019/0071)—is useful to ensure the removal of MPs at WWTPs. This framework also calls for the adoption of multiple technologies along the value chain.331 To control the growth of oyster aquaculture, the Chinese Taipei Shallow Sea Oyster Aquaculture Management Autonomous Regulations have been implemented. Specific clauses of the regulation encourage oyster farmers to use non-styrofoam buoys by providing subsidies, even though its main purpose is to handle the oyster aquaculture zoning system. The government took this step to stop styrofoam buoys from shedding MPs.332 A regional action plan was set up by HELCOM in 2015 to address marine litter and secondary MPs by 2025. By enhancing stormwater management and increasing the number of WWTPs, assessing primary sources and legal mechanisms to address them, promoting MP-free formulae, putting certification programs (like EU Ecolabel and Blue Angel) into place, encouraging no littering policies, supplanting primary MPs in personal care products, and increasing public awareness, this plan suggests ways to combat primary MPs.333 To lessen the negative environmental effects of plastic waste, the European Union has established in place an extensive set of policies.334 The European Union has banned single-use plastics and set broadened manufacturer responsibility and recycling standards for its member states.335 In Vietnam, several measures accompanied by particular laws are used to reduce the diffusion of MPs into the aquatic environment, particularly the riverine environment.336
Table 7 National strategies and regulations aimed at mitigating MP pollution, including plastic categories, policy actions, implementing countries, and targeted environmental goals337
Plastic category Policy Country Goal
Aquatic MPs Microbead-free waters act 2015 USA • Ban the production and sale of wash-off cosmetic products
Plastics The break free from plastic pollution act 2023 • Shift the financial responsibility of plastic waste management to producers of plastics
• Ban single use of plastic products
• Prohibit the export of plastic waste
Aquatic MPs Circular economy law (waste prevention and management) 2018 France • Ban cosmetic products containing plastic particles
Microfibers, microbeads Draft law on combating plastic pollution (adopted 2022) • Regulate the loss and leakage of industrial granules, prohibit intentional usage of microbeads in detergent, and provide impact assessment of plastic fibers on the textile industry
Larger plastics Single-use plastics prohibition regulations (2022) Canada • Prohibit the manufacture, importation, and distribution of single-use plastic products
Aquatic MPs Microbeads in toiletries regulations (2017) • Reduce the amount of plastic microbeads entering Canadian freshwater and marine environments
Larger plastics Plastic bag control and management regulations (2018) Kenya • Reduce usage, manufacture, and importation of plastic bags
The wildlife conservation and management act 2020 • Ban single-use plastic products
Aquatic MPs The plastic reduction and circular economy act 2021 Australia • Ban the distribution of wash-off personal care products
Aquatic MPs Waste minimization act through waste minimization (microbeads) regulations 2017 New Zealand • Prohibit plastic beads as an ingredient in personal care products
Larger plastics, aquatic MPs Environmental permitting regulations 2018 UK • Ban cosmetics and cleaning products containing microbeads
• Charge levies on single-use carrier bags
• Ban single-use plastics
Aquatic MPs The environmental protection (microbeads) (Northern Ireland) regulations 2018 Northern Ireland • Prohibit the use of plastic beads
Aquatic MPs 2019 industrial catalogue China • Ban the production and sale of cosmetics containing microbeads
Aquatic MPs The single-use plastics directive 2019 EU • Target eradicating the 10 most common single-use plastics found on the beaches and seas in Europe
Aquatic plastics Clean up The ocean cleanup • Developing technologies to reduce plastics in the ocean by 90% by 2040
Aquatic MPs, larger plastics Thailand ministry of public health (2019) through roadmap on plastic waste management (2018–2030) Thailand • Ban the production, sale, and distribution of cosmetics with microbeads as an ingredient
• Ban single use of plastics
Plastics waste Environmental management act (the commodities act decree) The Netherlands • Control packaging and consumer products
• Regulate single-use plastics
Aquatic MPs The microbeads (prohibition) act 2019 Ireland • Ban the use of plastic beads in households and industrial cleaning products
Larger plastics Plastic waste management (amendment) 2022 India • Phase out single-use plastics
Larger plastics The Germane ordinance on single-use plastics 2021 Germany • Reduce the impact of plastic waste on the environment
• Ban some single-use plastic products
Larger plastics The national environmental management waste act 2008 (amended 2014) through national waste management strategy 2020 South Africa • Reduce production of single-use plastics destroying the marine environment
Larger plastics Tax/levies on single-use plastics Wales, Ireland, Scotland • Discourage the single use of plastic products to reduce waste
Larger plastics The single-use foodware and litter reduction ordinance (2022) Berkeley, California • Reduce plastic waste in the environment


In addition to legislative measures, voluntary ecolabeling schemes such as the EU Ecolabel and Blue Angel play a significant role in promoting environmentally responsible technologies. These certifications assess products based on their entire life cycle—from raw material sourcing to end-of-life disposal.338 NC and biopolymer-based MP removal systems align with the criteria of these ecolabels, as they are derived from renewable resources, are biodegradable, and pose minimal toxicity risks to ecosystems.339,340 Also, these materials ensure that they break down naturally in the environment, minimizing long-term pollution.339 NC and biopolymers are generally less toxic compared to synthetic materials.341 Their production can also be optimized to reduce energy use and waste generation,342 thereby supporting circular economy goals.343 Importantly, alignment with such ecolabels may unlock policy-driven incentives, including subsidies, grants, or preferential procurement in public and private sectors. For example, ecolabel-certified technologies can benefit from EU-level funding schemes (e.g., Horizon Europe, LIFE Programme) and national green procurement strategies, encouraging broader adoption of natural MP removal methods.344,345

10. Conclusion and future outlook

Microplastics (MPs) are commonly found in water, posing risks to the environment and human health, which makes it crucial to find practical and sustainable methods for their removal. This review highlights the key role that natural compounds (NCs) and biopolymers can play in water treatment due to their unique properties. NC has a large surface area that effectively captures MPs and is biodegradable, making it an eco-friendly choice compared to synthetic materials. It works by sticking to, filtering, and clumping together pollutants. Biopolymers also help gather and separate MPs. When NC and biopolymers are used together, they often enhance the effectiveness of each other, resulting in better removal of MPs than when used separately. Even with these improvements, there are still significant areas of research that need to be addressed before these materials can be effectively utilized in real-life situations. First, improving the production, surface treatment, and blending of nanocomposites and biopolymers is essential to ensure strong performance across different types of MPs, particularly those with varying shapes and chemical compositions. It is essential to modify the surface properties of these materials to enhance their interactions with specific substances. In addition, limited research has been conducted on their long-term environmental behavior and potential ecological effects after use. Comprehensive assessments of their entire life cycle and environmental impact are necessary to ensure safe and sustainable large-scale application.

There is a significant gap in research regarding the identification, quantification, and understanding of nanoplastics. These tiny plastic particles can enter into our bodies and may be harmful. Unlike larger MPs, nanoplastics are more challenging to study because they are small, contain a mixture of materials, and their signals can be weak and difficult to detect. Some methods, like Raman spectroscopy and nanoscale FTIR, can help, but they need to be improved and made more sensitive. Clear guidelines are needed to ensure that results can be replicated and compared across different studies. Additionally, developing improved tools for imaging and analyzing nanoplastics in complex environments is crucial for accurately tracking these particles. Many studies to date have focused on specific areas of the environment, such as oceans, rivers, land, or the air, without adequately considering how MPs and nanoplastics move between these areas. Future research should adopt a broader perspective to understand how these particles travel and transform throughout the environment. This means investigating how MPs move from wastewater systems to soil when sludge is applied, from surface waters to living organisms, and through the interactions between air, soil, and water under different environmental conditions. It is also important to conduct experiments that consider various factors, such as pH, salt levels, organic matter, and temperature, to understand how these factors influence the removal of MPs and their behavior. Studies in regions with poorly managed plastic waste are critical, as these areas are major spots for MP pollution. Conducting pilot and large-scale studies is essential to bridge the gap between laboratory findings and real-world applications. Such studies should involve collaboration among researchers, industry professionals, policymakers, and local communities to jointly identify problems, design treatment systems, and share knowledge. Working together in this way not only makes the technology more relevant but also helps the community accept it and ensures it aligns with policies. It is also essential to test these treatment systems on a larger scale with various types of wastewaters, including those from cities and industries, to determine if they are practical and cost-effective.

The use of nanocellulose and biopolymer technologies in wastewater treatment plants presents exciting possibilities; however, careful consideration is required regarding their integration with existing systems. There are challenges, including the risk of clogging, increased operational complexity, and managing or recycling materials. A modular approach, which may include additional filtration steps utilizing these new materials, could provide flexibility while ensuring the primary treatment processes run smoothly. Future research should focus on developing scalable production methods, enhancing material durability under real wastewater conditions, and implementing long-term performance monitoring. Additionally, emerging technologies such as machine learning could enhance traditional treatment processes, potentially optimizing the management of wastewater through the use of these advanced materials.

The implementation of new ideas in real-world settings requires addressing several challenges, including financial constraints, technological limitations, and regulatory hurdles. Some of these challenges involve the high costs of producing bioplastics, differences in the sources of materials such as biomass, energy-intensive processing steps, and the lack of clear safety standards for waste materials. Policy-driven plans and cross-sector collaboration are essential to address these issues. Increasing production by utilizing eco-friendly chemistry, leveraging agricultural waste as raw materials, and exploring methods to reduce energy consumption in production can help lower costs and make processes more sustainable. At the same time, regulatory agencies should create clear guidelines to assess the safety and effectiveness of bioplastics and related technologies in environmental applications. Nanocellulose and biopolymers hold great potential for removing microplastics; however, effective utilization requires focused attention on several key areas. This includes improving materials for enhanced performance, developing more effective tools for detecting tiny plastics, and conducting real-world pilot studies to assess their effectiveness. It is also necessary to implement innovative monitoring systems that provide quick feedback during use. On the policy front, reducing microplastics can be achieved by linking wastewater management with solid waste processes, ensuring high standards in recycling, regulating new sources of microplastics, and raising public awareness. Addressing these challenges will be essential for making these solutions practical and environmentally friendly in tackling microplastic pollution in our water systems.

Author contributions

Sayam conceived the study, developed the methodology, wrote the original draft, created visualizations, and performed proofreading; Tarikul Islam conceived the study, developed the methodology, contributed to writing, editing, and reviewing the manuscript; conducted the investigation; prepared visualizations; supervised the project; curated data; validated results; and provided resources; Tasnim Hanan Tusti contributed to writing the original draft, prepared visualizations, edited the manuscript, curated data, and conducted formal analysis; Joyjit Ghosh contributed to writing and editing the manuscript and assisted with the literature review.

Conflicts of interest

The authors declare that they have no conflict of interest.

Data availability

All data related to the research are included in the manuscript.

Acknowledgements

The authors declare that they did not receive any internal or external funding for the research.

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Footnotes

Py-GC/MS: a thermoanalytical method that thermally decomposes polymers into fragments for identification via gas chromatography and mass spectrometry.
MFI: an optical technique for real-time, in situ analysis of suspended microplastic particles in liquids.

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