Remediation of Soil Contaminated with Microplastics: Strategies and Practical Implications
Abstract
1. Introduction
2. Review Methodology
3. Remediation Strategies
3.1. Physical Remediation
3.2. Chemical Remediation
| Method/Reference | Key Reagents/System | Mechanism | Remediation Targets | Performance | Additional Effects |
|---|---|---|---|---|---|
| DBD plasma (soil treatment) [49] | Dielectric barrier discharge plasma (air/N2, 17.5–24.1 kV)/ex situ; laboratory-scale plasma reactor system | ROS oxidize microplastics, causing chain scission and mineralization (CO2, H2O) | Microplastics (PE, PP, PS, and PVC) | Up to 96.5% microplastic removal in 30 min; energy efficiency ~19.03 mg kJ−1 | Efficiency depends on voltage, airflow, and ROS residence time |
| DBD plasma (PS-specific degradation) [50] | Plasma reactor (up to ~20 kV, controlled airflow)/ex situ; laboratory-scale plasma reactor | Two-stage oxidation: polymer fragmentation and ROS mineralization | PS microplastics | Up to 98.7% degradation in 60 min; ~90.6% converted to COx | Efficiency decreases at high microplastic loading; airflow optimization critical |
| Fast pyrolysis [51] | High temperature (400–500 °C)/ex situ; laboratory-scale thermal remediation system | Thermal decomposition of microplastics and co-contaminants; breakdown of polymers and dissolved organic matter interactions | Microplastics + petroleum hydrocarbons | 100% microplastic removal (≥400 °C); ~99% total petroleum hydrocarbon removal (500 °C, 15 min) | Restores soil properties; reduces microbial diversity but enriches functional taxa |
| Electrochemical coagulation (ECC) [53] | Fe electrodes (Fe3+ species)/ex situ; laboratory-scale electrochemical reactor treating runoff | Electrocoagulation: Fe hydroxides adsorb and flocculate microplastics, leading to removal via precipitation/flotation | Microplastics in runoff/soil leachate | ~98% microplastic removal in <45 min | Produces sludge containing microplastics; effective for fine particles |
| Kaolinite amendment [55] | Kaolinite (1–2%)/in situ; greenhouse pot experiment | Increases soil pH and cation exchange capacity, reduces metal bioavailability; modifies soil chemistry to limit microplastic-induced mobilization of Cd | Microplastics + Cd co-contamination | Reduces bioavailable Cd by 23.70–35.74%; reduces plant Cd by 9.65–30.86%; increases crop biomass by 8.40–40.59% | Restores pH (to ~7.79–8.03) and cation exchange capacity; mitigates microplastic-induced acidification |
| Fucoxanthin amendment [56] | Natural pigment (0.5–3%)/in situ; pot experiment | Microbial degradation releases organic acids, leading to pH buffering and nutrient mobilization | Microplastics (PS) | Increases organic matter to ~7.35%; increases N, P, K by up to 8.7%, 14.2%, 3.2% | Indirect remediation; enhances plant growth and soil fertility rather than degrading microplastics |
| Soil washing + electrocoagulation [58] | EDTA, FeCl3, oxalic acid, Aloe vera gel + electrocoagulation/ex situ; pilot-scale system | Chemical extraction of microplastics/heavy metals, followed by electrocoagulation to remove residuals | Microplastics + heavy metals | Up to 700 microplastics kg−1 removed (Aloe vera); high heavy metal removal (EDTA, FeCl3) | Integrated chemical system; cost-effective (~0.779 USD m−3) |
3.3. Biological Remediation
3.4. Hybrid Remediation
4. Practical Implications
4.1. Effectiveness
4.2. Scalability
4.3. Limitations and Future Directions
5. Conclusions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Acknowledgments
Conflicts of Interest
References
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| Method/Reference | Biological Agent/System | Mechanism | Remediation Targets | Performance | Additional Effects |
|---|---|---|---|---|---|
| Earthworm-mediated remediation [60,61] | Lumbricus terrestris, Metaphire guillelmi/in situ; mesocosm | Ingestion, gut fragmentation, depolymerization, bioturbation, microbial stimulation | LDPE, PLA, polybutylene adipate terephthalate (PBAT), PE, PVC | PLA depolymerization (weight-average molar mass decreases by 17.7%); increased small microplastics (e.g., LDPE from 8.4% to 18.8%); improved nutrients (0.2–36.1%) and enzyme activity (2.9–34.3%) | Enhances soil structure, fertility, microbial diversity, and plant growth |
| Vermicomposting [62] | Earthworms (e.g., Eisenia fetida) + microbes/ex situ; composting | Gut fragmentation + cast-associated microbial degradation; enrichment of polymer-degrading microbes | Biodegradable plastics in organic waste systems | Faster and more efficient than conventional composting (conceptual and qualitative) | Enriched with degraders (e.g., Streptomyces, Trichoderma) and enzymes |
| Earthworm gut bacteria bioaugmentation [63] | Microbacterium, Rhodococcus, Mycobacterium, Streptomyces, Bacillus/in situ; laboratory-scale soil microcosm experiment | Enzymatic biodegradation and metabolic breakdown (volatile organic compound production) | LDPE microplastics (~150 µm) | ~60% degradation in 21 days; particle size reduced to ~23.6–35.4 µm | Produces degradation metabolites (e.g., alkanes); confirms active polymer metabolism |
| Microbial consortia (bacteria + fungi) [64] | Bacillus cereus, Lysinibacillus fusiformis, Aspergillus sp./in situ; laboratory-scale soil inoculation | Oxidative degradation, polymer chain modification, surface erosion | PE microplastics + tetracycline | Fourier-transform infrared (FTIR)/X-ray diffraction (XRD) confirms oxidation; scanning electron microscopy (SEM) shows cracks and erosion | Co-contaminants (e.g., antibiotics) may inhibit degradation and alter soil cation exchange capacity |
| Composite microbial agent (CMA) [65] | Mixed bacteria & fungi (Bacillus, Trichoderma, etc.)/in situ; field-scale agricultural trials | Enzymatic depolymerization, additive degradation, microbial community restructuring | PE microplastics (field soils) | Reduces microplastic abundance by up to 8032 particles/kg | Enhances soil function, nutrient cycling, and plant growth |
| Enzyme–microbe synergistic system [66] | Immobilized laccase + Pseudomonas putida/in situ; greenhouse pot experiment | Enzymatic oxidation + microbial degradation | PE microplastics | ~21.38% degradation in 60 days | Increases microbial biomass, enzyme activity, plant growth, and photosynthesis |
| Reductive soil disinfection (RSD) [67] | Indigenous anaerobic microbes (stimulated)/In situ; pot experiment under controlled anaerobic incubation | Anaerobic decomposition, microbial restructuring, enzyme stimulation | PBAT, polybutylene succinate (PBS) microplastics | Improves Soil Quality Index; enhances enzyme activities | Shifts microbial community (Firmicutes increase); partial recovery after aeration |
| Microbial signaling (indole amendment) [68] | Indole-stimulated microbial communities/in situ; laboratory-scale experiment | Modulates quorum sensing, enhances diversity and stability | PE, PS microplastics | Increases diversity (Shannon ~7.07); mitigates microplastic-induced dysbiosis | Dose-dependent effects; enriches degraders (e.g., Pseudomonas) |
| Phytoremediation (rhizodegradation) [69] | Medicago sativa (alfalfa) + rhizosphere microbes/in situ; greenhouse pot experiment transitioning to semi-field conditions | Root exudates stimulate microbial degradation of microplastics | PET, PP microplastics | Low degradation (0.29–0.44%) over 12 months | Enhances microbial activity and soil enzymes |
| Plant–microbe bioaugmented phytoremediation [70] | Cymbopogon flexuosus + Micrococcus luteus/in situ; pot-scale greenhouse experiment | Rhizosphere co-metabolism; enhanced oxidation of microplastics | LDPE microplastics + petroleum hydrocarbons | Enhanced oxidation (FTIR evidence); total petroleum hydrocarbon removal up to 79.16% | Root exudates promote degradation hotspots |
| Plant growth-promoting bacteria-assisted remediation [71] | Bacillus sp., Enterobacter sp./in situ; pot-scale experiment | Plant growth promotion, stress alleviation, microbial community restructuring, Cd immobilization | PE microplastics + Cd | Reduces bioavailable Cd up to 45.8%; increases biomass up to ~46% | Improves nutrient availability and microbial stability |
| Method/Reference | Component/System | Mechanism | Remediation Targets | Performance | Additional Effects |
|---|---|---|---|---|---|
| Biochar–microbial stimulation [73] | Solidago canadensis-derived biochar—modified (SBM) and unmodified (SBU)/in situ; laboratory-scale experiment | Enhances nutrient cycling, microbial biomass, enzyme activity; restores soil biochemical functions | PE, PLA-contaminated soil | Increases NH4+ by 33.98%; increases NO3− by 66.02%; increases microbial biomass up to 57.67% | Improves C, N, P cycling and microbial metabolic efficiency (CUE) |
| Biochar–rhizosphere interaction [75] | Straw biochar (2%) + plant system/in situ; field scale agricultural experiment | Stimulates microbial functional genes and enzyme activity; enhances nutrient cycling and plant uptake | LDPE microplastics (low vs high levels) | Increases phoD abundance by 127.75%; increases alkaline phosphatase activity by 22.57%; increases root biomass by 52.80% | More effective at low microplastic levels; reshapes protist communities and ecological networks |
| Biochar–microbial community restoration [74] | Biochar + indigenous microbes/in situ; laboratory scale | Restores microbial structure, functional genes, and nutrient cycling | Microplastic-contaminated soil | Increases NH4+ & NO3− by 0.46–2.1×; increases dissolved organic carbon by 35.8–43.7%; increases functional microbes by up to 958.7% | Reverses microplastic-induced disruption of microbial networks and functions |
| Biochar–pollutant co-contamination control [77] | Biochar + microplastics + antibiotic (oxytetracycline)/in situ; controlled pot experiment | Adsorption of antibiotics and microplastics; reduces bioavailability and ARGs; mitigates toxicity | PE/PLA + oxytetracycline systems | Reduces oxytetracycline in soil (to ~16.05–19.76 mg/kg); reduces plant accumulation (~2.79–3.65 mg/kg) | PE competes for sorption sites; PLA enhances co-adsorption |
| Biochar–metal–plant system [78] | Biochar + microplastics + Cd + plants (Suaeda salsa)/in situ; controlled pot and wetland simulation experiment | Adsorption, ion exchange, microbial reshaping, phytostimulation | PE/PLA + Cd | Reduces bioavailable Cd by 14–15%; increases soil organic matter up to 130%; increases urease up to 183% | Improves soil fertility, enzyme activity, and plant growth |
| Biochar-based microbial inoculant (SynCom) [79] | Biochar + plant growth-promoting rhizobacteria (Pantoea, Pseudomonas, Bacillus)/in situ; pot-scale controlled greenhouse | Adsorption + microbial colonization + nutrient cycling + stress alleviation | Rubber microplastics | Increases yield by 81.41%; increases urease by 19.65%; increases dehydrogenase by 115.74% | Enhances plant growth, reduces oxidative stress, and restores soil fertility |
| Nano-material–phytoremediation [81] | C-nZVI + ryegrass (Lolium perenne)/in situ; controlled sediment pot experiment | Metal stabilization + enhanced plant uptake + enzyme activation + microbial stimulation | Microplastics + Cd co-contamination | Increases biomass up to 58.94%; increases Cd uptake up to 69.49%; increases residual Cd by 22.12–148.67% | Improves plant tolerance, nutrient status, and soil enzymatic activity |
| Remediation Strategy | Degradation/Removal Capacity | Scalability | Energy Requirement | Field Applicability | Risk of Secondary Pollution | Long-Term Sustainability |
|---|---|---|---|---|---|---|
| Adsorption using biochar | Moderate–high adsorption (>86% removal), but mainly immobilization rather than degradation | High; compatible with agricultural practices | Low | High; readily deployable in situ | Possible remobilization/desorption over time; incomplete mineralization | High if combined with biological degradation; reusable and low-cost |
| Nano-enabled remediation (S-nZVI, SA/nZVI-rGO barriers) | Moderate–high immobilization/removal (up to 81.55%; >98% for co-contaminants) | Moderate; constrained by material cost and dosing control | Moderate | Suitable for targeted in situ remediation and subsurface zones | Potential nanoparticle ecotoxicity and aggregation issues | Moderate; stabilization effective but long-term nanoparticle fate uncertain |
| DBD plasma treatment | Very high; near-complete degradation/mineralization (96.5–98.7%) | Low–moderate; mainly centralized or ex situ systems | Very high (high voltage plasma generation) | Limited for open-field soils; more suitable for engineered facilities | Low residual microplastics after mineralization, but potential disturbance to soil biota and high energy footprint | Moderate; effective removal but constrained by energy demand and infrastructure |
| Fast pyrolysis | Very high; near-complete degradation/removal | Low; requires centralized thermal reactors | Very high (≥400 °C heating) | Primarily ex situ | Potential alteration of soil microbial communities and emissions if poorly managed | Moderate; efficient destruction but limited by energy intensity |
| ECC/soil washing–coagulation | Very high (~98% removal) | Moderate; feasible in engineered treatment systems | Moderate–high | Mostly ex situ; difficult for large agricultural fields | Generates microplastic-containing sludge and chemical residues (e.g., EDTA and FeCl3) | Moderate; effective removal, but waste management is required |
| Earthworm-mediated remediation | Low–moderate; promotes fragmentation and partial depolymerization | High; self-sustaining biological process | Very low | High in agricultural soils | High risk of fragmentation into nanoplastics and vertical redistribution/leaching | Moderate; environmentally compatible but may increase contaminant mobility |
| Microbial biodegradation/bioaugmentation | Moderate; up to ~60% degradation under optimized conditions | High; microorganisms proliferate in situ | Low | High but dependent on environmental conditions | Possible formation of smaller plastic fragments during incomplete degradation | High if stable microbial activity is maintained |
| Enzyme–microbe synergistic systems | Moderate (~21.4% degradation over 60 days) | Moderate | Low–moderate | Potentially suitable in situ, though still experimental | Incomplete mineralization may generate nanoplastics | High potential if enzyme engineering improves degradation efficiency |
| Phytoremediation/plant–rhizosphere systems | Low direct removal; mainly indirect degradation stimulation | High | Low | Very high for agricultural soils | Limited direct pollution risk, though fragmented plastics may persist | High; improves soil ecological functions and supports long-term restoration |
| Biochar–microbe hybrid systems (e.g., SynCom) | Low direct removal; mainly stress mitigation and indirect degradation enhancement | Very high | Low | Very high; easily integrated into farming practices | Lower risk than purely physicochemical methods, though microplastics may remain adsorbed to biochar | Very high; enhances microbial activity, nutrient cycling, and soil resilience |
| Biochar–plant hybrid systems | Low direct removal; promotes rhizosphere-assisted transformation | Very high | Low | Very high; compatible with field-scale agriculture | Limited secondary pollution risk, though microplastics are not fully mineralized | Very high; supports ecological restoration and sustained soil functioning |
| Integrated hybrid systems (biochar + nanomaterials + microbes/plants) | Moderate–high combined removal, immobilization, and degradation potential | High potential but still emerging | Moderate | Promising for field-scale applications if optimized | Risk depends on nanomaterial use and incomplete degradation products | Very high potential due to combined rapid stabilization and long-term biodegradation |
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Tang, K.H.D. Remediation of Soil Contaminated with Microplastics: Strategies and Practical Implications. Environ. Remediat. 2026, 1, 5. https://doi.org/10.3390/environremediat1010005
Tang KHD. Remediation of Soil Contaminated with Microplastics: Strategies and Practical Implications. Environmental Remediation. 2026; 1(1):5. https://doi.org/10.3390/environremediat1010005
Chicago/Turabian StyleTang, Kuok Ho Daniel. 2026. "Remediation of Soil Contaminated with Microplastics: Strategies and Practical Implications" Environmental Remediation 1, no. 1: 5. https://doi.org/10.3390/environremediat1010005
APA StyleTang, K. H. D. (2026). Remediation of Soil Contaminated with Microplastics: Strategies and Practical Implications. Environmental Remediation, 1(1), 5. https://doi.org/10.3390/environremediat1010005

