Next Article in Journal
Assessing the Chlorophyll-a Retrieval Capabilities of Sentinel 3A OLCI Images for the Monitoring of Coastal Waters in Algoa and Francis Bays, South Africa
Next Article in Special Issue
Pesticides, Heavy Metals and Plasticizers: Contamination and Risk Assessment of Drinking-Water Quality
Previous Article in Journal
Policy Chain of Energy Transition from Economic and Innovative Perspectives: Conceptual Framework and Consistency Analysis
Previous Article in Special Issue
Exposure Concentrations and Inhalation Risk of Submicron Particles in a Gasoline Station—A Pilot Study
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Systematic Review of Degradation Processes for Microplastics: Progress and Prospects

Key Laboratory of Coarse Cereal Processing, Ministry of Agriculture and Rural Affairs, Sichuan Engineering & Technology Research Center of Coarse Cereal Industrialization, School of Food and Biological Engineering, Chengdu University, Chengdu 610106, China
*
Author to whom correspondence should be addressed.
Sustainability 2023, 15(17), 12698; https://doi.org/10.3390/su151712698
Submission received: 24 June 2023 / Revised: 11 August 2023 / Accepted: 20 August 2023 / Published: 22 August 2023
(This article belongs to the Special Issue Urban Environment and Human Health)

Abstract

:
Microplastics (MPs) have been shown to be more hazardous than large plastics. In recent years, many studies have confirmed the hazards of MPs to organisms and summarized various MP degradation techniques, but there is a lack of discussion on the prospects of the application of these degradation techniques and their degradation efficiency. Therefore, this paper reviewed the degradation techniques of MPs, such as adsorption, direct photodegradation, photocatalytic oxidation, electrochemical oxidation, and biological methods, and their application prospects. By focusing on the biodegradation mechanism and degradation efficiency, the potential for efficient and sustainable development of biodegradation processes and the prospect of large-scale application are highlighted, enabling readers to better understand the current status of research on MP biodegradation. This review provides direction for research on MP degradation, suggestions for governmental environmental governance and policy development, and references for the sustainability and large-scale application of MP biodegradation.

Graphical Abstract

1. Introduction

Due to their low price, extreme durability, light weight, and good ductility, plastics are now widely used in the construction, healthcare, electronic components, automotive, agriculture, and food packaging industries [1,2,3,4]. And because of the durability of plastics, they also pose a huge environmental hazard. Studies have shown that global plastic waste is expected to reach 270 million tons by 2060 [5]. Waste plastics undergo physical, chemical, biological, and other forms of wear, consumption, and decomposition, resulting in particles less than 5 mm in diameter being defined as microplastics (MPs) and particles less than 100 nm being defined as nanoparticles (NPs) [6,7,8,9]. Figure 1 shows the source of microplastics. Plastic particles, cosmetics, laundry wastewater, sewage sludge, and atmospheric deposition generated during the friction between motor tires and road surfaces are also important sources of MPs [10,11,12].
MPs can be absorbed by aquatic plants and animals and adversely affect their growth, development, and reproduction [13,14,15,16,17,18,19,20]. On the other hand, MPs can absorb various pollutants in the ocean, such as antibiotics [21,22], polycyclic aromatic hydrocarbons [23,24], heavy metals [25,26,27], organic compounds [28,29], and pathogenic microorganisms [30,31,32], and are capable of serving as carriers of pollutants that are fed on by aquatic organisms and thus entering the organisms. In addition, MPs can directly enter agricultural soils through sewage sludge, irrigation water, domestic water, and atmospheric deposition, or indirectly enter agricultural soils through the degradation of plastic residues (such as mulch films) in agricultural activities. Figure 2 shows the pathway of MPs into plants. When absorbed by terrestrial plants, MPs will inhibit the growth and development of the plants and remain in the plant bodies. The accumulation of MPs in the plant body will eventually reach the human body along with the enrichment of the food chain, causing harm to the human body.
At present, most of the waste plastics in the world are disposed of in landfills [33], which require a large amount of land. Due to the strong stability of plastic, it is not easy to decompose in the soil, which seriously affects the sustainable use of the soil. Moreover, a large number of microorganisms breed in the soil, producing harmful gases that adversely affect the surrounding air and environment [34]. Not only that, but the leachate from plastic waste will also enter the river through groundwater, causing harm to the environment and ecology. With the deepening of research, there are an increasing number of treatment methods for waste plastics. The MPs contained in the sewage treated by the sewage treatment plant are reduced, but there are still many small particles that are difficult to remove. Adsorption, advanced oxidation processes (AOPs), and biodegradation can accelerate the degradation of MPs through a series of physical and chemical reactions, thus increasing their degradation rate [35,36]. Among them, AOPs include direct photodegradation, photocatalytic oxidation, and electrochemical oxidation. However, there are shortcomings to these methods. The process of photodegradation is uncontrollable. Even under laboratory conditions, the degree of photoaging and the types of intermediates in the photochemical system cannot be completely determined. In addition, photodegradation consumes more energy. Prolonged exposure to sunlight may also cause light pollution [37]. For photocatalytic oxidation, although it uses free solar energy, most plastics can only be partially degraded under ultraviolet radiation, and the degree of degradation is not up to the requirements. The catalyst added in the reaction is also difficult to recover and can easily result in secondary pollution [35]. Electrochemical oxidation has broad application prospects in the treatment of degradable plastics due to its strong controllability, simple operation, and low secondary pollution. However, for these processes, the intermediate products obtained by their degradation are uncertain as to whether they are harmful or not, and it is difficult to control the reaction process. Therefore, much research is being conducted on the biodegradation process. MPs can serve as substrates for microbial biofilm growth and provide energy for microbial growth and reproduction. And the selection of biodegradation conditions is a key factor in improving the efficiency of degradation. pH is a critical factor for the survival of microorganisms, as it has a key influence on their life activities and substance metabolism [38]. An increase or decrease in pH during biodegradation may be due to the production and accumulation of alkaline aromatic compounds or other metabolites during degradation. As the biofilm grows, the plastic structure breaks, and during the assimilation process, it is taken up by the microorganisms (bacteria, fungi) in the biofilm and finally decomposed into smaller molecules (CO, N2, H2, H2O, H2S) [39]. These molecules are further used by microorganisms as a usable energy source and eventually returned to the atmosphere, completing the conversion from small molecules to usable products [35]. Not only is it better than other processes in terms of energy savings, environmental pollution, and degradation efficiency, but the biodegradation of its intermediate products and final products will not cause secondary pollution, which is a more efficient and ideal degradation process. Therefore, bioremediation is also considered to be the most ideal method for removing MP contamination.
In general, a problem that human beings must face is that MPs will only be produced by humans, and after a series of migrations, they will eventually return to humans. With the passage of time and the accumulation of MPs, it is time to think about and solve these problems. As of May 2022, a total of 113 articles on microplastic degradation were found through a literature analysis performed using the Stork software (https://www.storkapp.me, accessed on 23 June 2023) and screening of article titles and abstracts. By analyzing the above articles, this study reviews various degradation techniques for MPs and discusses for the first time the efficiency, sustainability, and prospects for large-scale application of biodegradation methods. This review provides direction for research on the degradation of MPs, suggestions for governmental environmental governance and policy development, and references for the sustainability and large-scale application of MP biodegradation.

2. Physical and Chemical Processes

MPs are considered more serious persistent pollutants than plastics [40]. In the past ten years, China and European countries have taken corresponding measures to limit the use of plastics by issuing laws and regulations to reduce the pollution of MPs from the source [35]. However, the situation of plastic pollution around the world is still serious. In recent years, many studies have reported the degradation processes of MPs. These include physical and chemical methods.

2.1. Physical Law

Physical methods mainly include sol–gel, coagulation filtration, and adsorption. Structural composite silica gel is obtained by the sol–gel process to polymerize and interact with MPs [41,42], and then separation technology is used to eliminate these agglomerates to eliminate the MPs. Coagulation filtration causes MPs to form larger agglomerates through coagulation to achieve the separation effect. The sol–gel process exhibits a pH-induced reaction and is more suitable for application in liquids [43]. Excessive use of coagulants will cause secondary pollution and harm organisms. Leppänen et al. [44] captured microplastics in the water column using a hygroscopic nanocellulose network. In addition, for a long time, biochar has been regarded as the most promising adsorbent due to its porous structure and easy fabrication, and the adsorption of pollutants has been widely studied [45,46]. MPs can be adsorbed by different adsorbent materials through mechanisms including electrostatic interactions, hydrogen bonding interactions, and π-π interactions. Wang et al. [47] studied a highly efficient Mg/Zn-modified magnetic biochar adsorbent for the removal of MPs from aqueous solutions with a maximum efficiency of 99.46%. Tiwari et al. [48] studied the interaction between a Zn–Al layered double hydroxide (LDH) and MPs, indicating that the Zn–Al–LDH can adsorb MPs in water and that its efficiency can reach 164.49 mg/g. Sun et al. [49] found that a sponge made of chitin and graphene oxide (ChGO) as raw materials can effectively adsorb different types of MPs. Even after multiple adsorption cycles, its efficiency can still reach 89.8%. Both magnetic and composite adsorbents have ideal removal efficiencies, but their material synthesis is complex and the cost is high; additionally, more research is needed to explore the adsorption mechanism of MPs; therefore, the development of MPs adsorbents will still be the focus of attention [50].

2.2. Advanced Oxidation Processes (AOPs) Degradation

Some recent studies have shown that AOPs are an efficient chemical elimination technology that can lead to the formation of various reactive oxygen species (ROS), chemical chain scission, or cross-linking and exhibit excellent performance in degrading MPs [51,52]. AOPs include three main methods: Direct photodegradation, photocatalytic oxidation, and electrochemical oxidation. The oxidation process, degradation mechanism, advantages and disadvantages, and future application prospects of the three processes will be discussed in detail below.

2.2.1. Direct Photodegradation

Direct photodegradation is the main transformation pathway of atmospheric organic matter and is considered an important process in the decomposition of hydrocarbons and polymers [53,54]. At present, the degradation of MPs has also been studied. Different types of light are important factors influencing the photodegradation of MPs, with UV light having the greatest effect [55]. Under strong UV irradiation, MPs can cause UV absorption of unsaturated surface groups, formation of polymer radicals, oxidation, hydrogen extraction, and chain scission or crosslinking [56,57]. Ainali et al. [58] analyzed pyrolysis-gas chromatography–mass spectrometry (Py-GC/MS), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), differential scanning calorimetry (DSC), scanning electron microscopy (SEM), and other methods to observe and analyze the degradation process of MPs. FTIR revealed that MPs formed new functional groups during UV irradiation, including carbonyl, vinyl, and hydroxyl/hydroperoxides, and XRD and DSC measurements enhanced the apparent effect of UV irradiation on their crystalline and thermal properties [58]. SEM found significant morphological changes on the surface of MPs, demonstrating the degradation of plastic properties and their progressive fragility due to UV irradiation [58]. In addition, the plastic degradation mechanisms of different types of MPs before and after UV irradiation were investigated by Py-GC/MS, demonstrating that the respective quantitative ratios of low molecular weight compounds and relatively high molecular weight hydrocarbons varied with UV irradiation [58]. Zhu et al. [37] studied PS-MPs after simulating sunlight for 150 days and observed obvious signs of aging: the surface roughness increased, and the particle size decreased. Ding et al. [59] found that soils with different properties had different degradation rates during the same photodegradation process. The soil containing clay, iron oxides, and MnO2 enhanced the degradation rate, while the soil containing organic carbon inhibited the degradation rate. Electrostatic interactions may be the dominant factor influencing the rate of photodegradation of MPs in soils with different properties. Wang et al. [60] found that natural organic acids in the aqueous environment can promote the aging of PVC microplastics, which may be related to the hydroxyl radicals produced by the photolysis of these organic acids. Although modern technology can realize the degradation of MPs by artificial light sources, according to current research, its degradation efficiency cannot reach 100%. Coupled with its aging degree and the uncertainty of the type of intermediate products in this photochemical system, it may be harmful to the environment, causing secondary damage or even more harmful effects. It has been reported that the residues of photodegraded MPs can cause serious harm to organisms [61,62,63]. In recent years, some studies have shown that the photocatalytic reaction based on Mie resonance can lead to the coupling reaction of carbon–carbon (C–C) in an aromatic polymer that can achieve a degradation effect [64,65]. In addition, Kwon et al. [66] synthesized different Cu2−xS nanoparticles (CuS and Cu1.8S NPs) with localized surface plasmon resonance (LSPR) absorbance in the near-infrared (NIR) region and photodegradation properties leading to polydimethylsiloxane (PDMS) polymer. In addition, photodegradation causes a slight amount of pollution in the environment. The emergence of new technologies offers new ideas for the degradation of polymers. Therefore, future research should focus on the toxicological analysis of intermediates in the photodegradation process and the development and application of new technologies.

2.2.2. Photocatalytic Oxidation

Photocatalytic oxidative degradation is a redox process that uses solar energy as an energy source and utilizes the free radicals generated by semiconductors to react with MPs to break the polymer chain, thereby initiating the degradation process of the MPs in order to achieve the effect of removal [67]. At present, numerous studies have shown that nano-TiO2 can be used in the photocatalytic degradation of MPs. The process is accompanied by the generation of hydroxyl, carbonyl, and hydrocarbon groups, resulting in a harder surface [68,69]. Nabi et al. [68] showed in their 2020 paper that the TiO2 nanoparticle film had a high degradation efficiency of 98.40% for 400 nm PS within 12 h and the highest degradation efficiency for PE after 36 h. In addition, it was mentioned in a paper in 2021 that N–TiO2 materials synthesized by two routes showed a good degradation effect on MPs [70]. Not only on nano-TiO2, Tofa et al. [70] found in 2019 that zinc oxide (ZnO) nanorods (ZnO-Pt) also have a good effect on the degradation of MPs in water. The use of solar energy as an energy source is the greatest advantage of photocatalytic oxidation. Cao et al. [71] successfully prepared a series of MXene/ZnxCd1-xS photocatalysts in 2022, which can degrade MPs and utilize light energy to catalyze hydrogen evolution. The optimal photocatalytic hydrogen evolution rate can reach 14.17 mmol/g/h, which solves the pollution and energy problems of MPs in one fell swoop. Zhou et al. [72] concluded that Cu2O is an excellent visible-light photocatalyst. In 2021, Zhu et al. [73] successfully prepared a material (rGO@Fe3O4/Cu2O@ZnO) with strong hydrophobicity, high photocatalytic performance, and recyclability, and its photocatalytic degradation efficiency of acrylamide (AM) reached 97.3%. In addition to this, a large number of studies have reported the study of photocatalysts such as Cu2O [74,75], α-Fe2O3 [76,77], Au [78], Ag [79], and Cu [80] for polymer degradation. Photocatalytic oxidation can utilize solar energy and save energy. It is economically feasible to apply on a large scale, but the photocatalytic oxidation process may release volatile organic compounds (VOCs), which will inevitably have an impact on the environment. In addition, the catalyst is not easy to recycle, and the residue in the water will cause secondary pollution. Therefore, the future application of photocatalytic oxidative degradation technology needs further research.

2.2.3. Electrochemical Oxidation

At present, there are few studies on the effective degradation of MPs by electrochemical oxidation treatment. Miao et al. [81] proposed a similar electro-Fenton degradation method for MPs based on a TiO2/graphite (TiO2/C) cathode, which also generates free radicals through electrode redox to react with the MPs and achieve degradation. This method will not result in secondary pollution, but its electrolysis intermediates are uncontrollable. Therefore, future research should focus on controlling the environmental impact of intermediates and final decomposition products.

3. Biodegradation Processes

Biodegradation technology has the characteristics of high efficiency, being green, low cost, and sustainable development, and is considered to be the most likely technology to be applied to solve the pollution of MPs in the future. Although MPs can persist in the environment and have a certain resistance to degradation due to their chemical stability, studies have shown that some bacteria and fungi can participate in the degradation of MPs [82]. In addition, animals also have a certain degradation effect on MPs.

3.1. Animals

Animals can degrade MPs through phagocytosis or enzymes secreted by microorganisms in vivo. Figure 3 summarizes the process of MP removal in animals. Some studies have reported that yellow mealworms can survive by eating PS, which leads to a decrease in the quality of PS [83]. Baeza et al. [84] found that MPs were present in Lumbricus terrestris living in soil contaminated with MPs, and the number of particles in the hindgut was higher. Songet et al. [85] studied the invertebrate snail (Achatina fulica) in soil and found that it also had a certain ability to degrade PS. Only a few animals achieve degradation through ingestion, and most animals achieve degradation through enzymes secreted by their microbiota. Billen et al. [86] showed that both animal mealworms (Tenebrio molitor) and larvae of the greater wax moth (Galleria mellonella) accelerated the biodegradation efficiency of PE. To explore its specific degradation pathway, Zhang et al. [87] isolated a PE-degrading fungus from the gut of the wax moth Galleria mellonella and found that it had a significant effect on degrading PE-MPs. In addition, Luo et al. [88] found that larvae of Zophobas atratus (Coleoptera: Tenebrionidae) have certain degradation effects on three types of polystyrene (PS), PE, and polyurethane (PU), and their degradation is related to changes in the intestinal microbial community and digestive enzyme activity. Most of the degradation ability of animals is determined by the microorganisms in their bodies, so microbial degradation is worthy of our attention.

3.2. Bacteria

Bacteria are efficient degrading microorganisms capable of degrading MPs [89]. The degradation of MPs is closely related to enzymes produced by microorganisms [90]. Bacteria decompose organic polymers into simple CO2, H2O, and inorganic substances by secreting enzymes; this is the product obtained by combining enzymes with polymers and catalyzing their hydrolysis [91]. In the process of degradation, MPs are regarded as one of the essential carbon sources necessary for bacterial survival. Bacteria attach to the surface of MPs and form a biofilm, which leads to the corrosion and cracking of the MPs. As the bacteria survive and reproduce on the biofilm, they continue to soften the MP structure and finally absorb it to achieve the purpose of removal (see Figure 4 for details). Diverse types of bacteria secrete different types of enzymes, which have different degradation effects and degradation products on various types of MPs. According to reports, bacteria may release toxic and harmful substances during the degradation process to inhibit their growth [36]. In addition, the enzymes secreted by bacteria may not work on different types of plastic substrates, and it is difficult to degrade MPs. Therefore, different kinds of efficient degrading bacteria have been found continuously, which improve the degradation efficiency of MPs [92]. The bacteria currently capable of degrading MPs are summarized in Table 1.
The microbial degradation of PE-MPs, PS-MPs, PP-MPs, PET-MPs, PVC-MPs, etc., has attracted extensive attention. The intestinal tract of animals is the main gathering place for microorganisms, and some studies have found that bacteria isolated from the intestines can effectively degrade MPs. Yin et al. [93] isolated Acinetobacter sp. strain NyZ450 and Bacillus sp. strain NyZ451 from Tenebrio molitor larvae. After the two were co-cultured for 30 days, the quality of the PE decreased by approximately 18%. Yang et al. [94] also isolated a PS-degrading strain, Exiguobacterium sp. Strain YT2, from the Tenebrio molitor larvae. It could form biofilms on PS membranes during a 28-day incubation period. Through experiments, it was found that the suspension culture of its strains could reduce the weight of PS by 7.4% within 60 days. Lwanga et al. [95] also isolated bacteria from the gut of earthworms that had a degradation effect on LDPE-MPs. Microorganisms can use MPs as a source of energy to survive. Therefore, Vimala et al. [96] used PE as the sole carbon source to study the degradation efficiency of Bacillus subtilis, and the results showed that its mass was reduced by 9.26% after 30 days.
The soil is rich in nutrients and is the main gathering place for bacteria; furthermore, it is the main area of pollution. Therefore, a large number of researchers have screened for an efficient MP-degrading bacterium in the soil. Park et al. [97] added a mixed flora to the sediments of the landfill site as the basic culture medium (without a carbon source) and screened the viable strains by adding PE MPs. Finally, the content of Bacillus and Bacteroides isolates was higher, which reduced the weight of PE MPs by 14.7%. Auta et al. [98] isolated Bacillus cereus and Bacillus gottheili from the sediments of mangroves in Malaysia. After 40 days of culture, Bacillus cereus caused a massive reduction in PE, PET, and PS to 1.6%. B. gottellii caused PE, PET, PP, and PS weight loss percentages of 6.6%, 7.4%, 3.6%, and 5.8%, respectively [98]. Auta et al. [99] isolated mixed colonies from mangroves in different environments, and after adding PS and PET for 90 days, the weight loss reached 18%. To screen for more efficient degrading bacteria of PP-MPs, Auta et al. [100] isolated Bacillus sp. strain 27 and Rhodococcus sp. strain 36 from the Matang Mangrove area in Perak and the Cherating Mangrove area in Pahang in Peninsular Malaysia. The study showed that both bacteria could use PP-MPs for growth and reproduction, and after 40 days of culture, their weight loss rates were 4.0% and 6.4%, respectively [100].
Different bacteria have suitable conditions for their growth, and the influence of temperature on them cannot be ignored [101,102]. With an increase or decrease in temperature, the performance of bacteria’s in vivo adaptation to the environment is distinct, so the degradation effect of MPs may be different. Sun et al. [103] studied the effect of microorganisms on the degradation of PE, PVC, and PHA-MPs before and after composting. The results showed that the abundance of PE, PVC, and PHA-MPs decreased after composting, and the MPs were oxidized, with their oxygen content increasing by 3–30%. The surface morphology was rougher than that of the initial MPs, and obvious cracks and grooves were observed in all of them. This shows that the composting technology can degrade MPs, resulting in a weight reduction of 13%, 3%, and 29%, respectively [104]. Chen et al. [104] used high-temperature composting (HTC) technology to accelerate the microbial degradation of MPs in sewage sludge. Thermus, Bacillus, and Geobacillus were the dominant strains for efficient degradation during HTC [105]. After 45 days of culture, the degradation efficiency reached 43.7%, and after co-culturing PS-MPs with bacteria at 70 °C for 56 days under laboratory conditions, the degradation rate was 7.3% [104]. Novel thermophilic bacteria have become the focus of research. Skariyachan et al. [106] screened eight strains of plastic-degrading bacteria after culturing 36 strains of plastic-degrading bacteria collected from sewage treatment plants, landfills, and other areas at 50 ℃ for 140 days. Then, a mixed bacterial colony was formed through various combinations. Finally, it was found that the degradation efficiency of four combinations, Aneurinibacillus aneurinilyticus btDSCE01, Brevibacillus agri btDSCE02, Brevibacillus sp. btDSCE03, and Brevibacillus brevis btDSCE04, was higher than that of the other groups and caused the weight losses of LDPE, HDPE, and PP to reach 58.21%, 46.6%, and 56.3%, respectively [106]. In contrast, Habib et al. [107] isolated two bacteria, Pseudomonas sp. ADL15 and Rhodococcus sp. ADL36, from the Antarctic soil. Infrared spectroscopy analysis showed that the functional groups of PP-MPs changed significantly after they were cultured with the Antarctic strain for 40 days, and the two bacteria reduced the weight of PP-MPs by 17.3% and 7.3%, respectively.
In addition to bacteria isolated from soil, a large number of microorganisms that can degrade MPs are also enriched in sewages, rivers, and oceans. Grgic et al. [108] isolated a mixed strain of Bacillus licheniformis, Lysinibacillus mas-siliensis, Delftia acidovorans, and Bacillus sp. from sludge and sediment in sewage treatment plants and studied their effect on LDPE-MPs and the PS degradation efficiency of MPs. After 22 days of culture, the results showed that mixed bacterial cultures degraded LDPE-MPs and PS-MPs better than pure bacterial cultures, and the biodegradation efficiency of LDPE-MPs was higher than that of PS-MPs [108]. Devi et al. [109] isolated four bacteria from the Vaigai River in Madurai, India, including Bacillus sp. (BS-1), Bacillus cereus (BC), Bacillus sp. (BS-2), and Bacillus paramycoides (BP). The results showed that a single colony had high degradation of PE and PP and that Bacillus paramycoides (BP) and Bacillus cereus (BC) reduced the weight of PP and PE by 78.99% and 63%, respectively [109]. Li et al. [110] isolated strain M. hydropicus ire-31 from a lignin-rich marine pulp mill. After culturing for 30 days, the changes in surface morphology and functional groups of PE-MPs were analyzed by SEM and FTIR, and cracks were observed on the surface. Using FTIR, it was found that additional hydroxyl and carbonyl functional groups were formed on the surface of the polymer, indicating that it had a degradation effect on PE-MPs through oxidation. Giacomucci et al. [111] studied the biodegradation of PVC by anaerobic microorganisms in the ocean. After 7 months of cultivation, a dense biofilm was displayed on the polymer surface with a weight loss of 11.7%, and the thermal stability and average molecular weight were significantly reduced, indicating the potential degradation effect of anaerobic microorganisms on PVC-MPs.
Harshvardhan et al. [112] isolated three marine bacteria from the Arabian Sea in India, named Kocuria palustris M16, Bacillus pumilus M27, and Bacillus subtilis H1584. After 30 days of growth in a medium containing PE as the sole carbon source, it was found by FTIR that the ketone carbonyl bond index, ester carbonyl bond index, and vinyl bond index on the surface of PE had increased, indicating the degradation effect of PE, which resulted in a weight loss of 1%, 1.5%, and 1.75%, respectively [112]. Raghul et al. [113] isolated V. parahaemolyticus (BTTV4 and BTTN18) and V. alginolyticus (BTTC10 and BTTC27) from marine sediments and studied their degradation efficiency of a polyvinyl alcohol-low linear density polyethylene (PVA-LLDPE) blend plastic film as a combination. After 15 weeks of incubation at 120 rpm and 37 °C in shake flasks, SEM showed that visible cracks and grooves appeared on the surface of the PVA-LLDPE blend film, indicating that the combination could lead to the degradation of the PVA-LLDPE plastic blend [113]. The study also pointed out that the percentage of tensile strength loss of PVA-LLDPE plastic films containing 25% and 30% PVA was greater, and the tensile strength decreased with increasing PVA content, indicating that the PVA component can be used as a carbon source to promote the degradation of PVA-LLDPE by bacteria [113]. Gao et al. [114] screened plastic debris-contaminated marine sediment samples collected from a bay in China and found a marine bacterial community, CAS6, that efficiently colonized and degraded PET and PE. Biofilms were found on the surface of PET and PE films by SEM, and significant changes in the surface morphology of PET and PE were observed, especially severe cracks and deep pores [114]. Soil and oceans are the main habitats of bacteria, which bring together a large number of MP-degrading bacteria. MPs are used by bacteria as the energy needed for growth to form biofilms on their surfaces. With the growth of biofilms, the surface of MPs will be cracked and damaged, and the changes in functional groups show the process of oxidation. Bacterial degradation has the advantages of being green, environmentally friendly, and sustainable, and numerous studies have proven the efficacy of efficient degradation of polysulfonic acid mucopolysaccharides by bacteria [115,116]. In future research, we should pay attention to the study of degradation efficiency and degradation mechanisms of bacterial degradation methods so that they have a better prospect for environmental governance and sustainable development.
Table 1. Research status of bacterial degradation of MPs.
Table 1. Research status of bacterial degradation of MPs.
The Bacteria TypesTypes
of MPs
Duration of
Degradation
Weight LossReferences
Acinetobacter sp. NyZ450/Bacillus sp. NyZ451PE30 d18%[93]
Exiguobacterium sp. YT2PS60 d7.4%[94]
Bacillus simplex, and Bacillus sp.LDPE21 d [95]
Bacillus subtilisPE30 d9.26%[96]
Bacillus sp. and Paenibacillus sp.PE60 d14.7%[97]
Bacillus cereusPE/PET/PS40 d1.6%/6.6%/7.4%[98]
Bacillus gottheiliiPE/PET/PP/PS40 d6.2%/3.0%/3.6%/5.8%[98]
B. cereus, S. globispora and B. flexus and B. gottheiliiPS and PET90 d18%[99]
Bacillus sp. 27PP40 d4.0%[100]
Rhodococcus sp. 36PP40 d6.4%[100]
Firmicutes, Bacteroidetes, Proteobacteria, Gemmatimonadetes, Deinococcus-ThermusPE/PVC/PHA60 d13%/3%/29%[103]
Thermus, Bacillus, and GeobacillusPS56 d7.3%[104]
Aneurinibacillus aneurinilyticus btDSCE01, Brevibacillus agri btDSCE02, Brevibacillus sp. btDSCE03, and Brevibacillus brevis btDSCE04LDPE/HDPE/PP140 d58.21%/46.6%/56.3%[106]
Pseudomonas sp. ADL15PP40 d17.3%[107]
Rhodococcus sp.PP40 d7.3%[107]
Bacillus licheniformis/Lysinibacillus mas-siliensis, Bacillus sp. and Delftia acidovaransLDPE and PS22 d [108]
Bacillus paramycoides (BP)PP21 d78.99%[109]
Bacillus cereus (BC)PE21 d63%[109]
Bacillus paramycoides (BP) and Bacillus cereus (BC)PP/PE21 d78.62%/72.50%[109]
M. hydrolyticus IRE-31LDPE30 d [110]
Anaerobic bacteriaPVC210 d11.7%[111]
Kocuria palustris M16PE30 d1%[112]
Bacillus pumilus M27PE30 d1.5%[112]
Bacillus subtilis H1584PE30 d1.75%[112]
V. parahaemolyticus (BTTV4 and BTTN18) and V.alginolyticus (BTTC10 and BTTC27)PVA-LLDPE105 d [113]
Exiguobacterium sp., Halomonas sp., and Ochrobactrum sp.PET/PE28 d2.7%/19.6%[114]

3.3. Fungi

In addition to bacteria, fungi have the potential to adhere to and utilize MPs [117]. Few studies have been reported on the degradation of MPs by fungi, which suggests there are some difficulties in screening fungal strains with MP-degrading properties [92]. However, in recent years, many researchers have screened out fungi that can degrade MPs from different places, mainly from soil and the ocean. The ability of fungi to degrade polymers is due to several extracellular enzymes secreted by their enzymatic systems, including a manganese peroxidase (MnP), a lignin peroxidase (LiP), a multifunctional peroxidase, and a laccase (Lac). The polymer is decomposed by these enzymes to produce monomeric substances, and these monomers are then absorbed by the fungus and assimilated or mineralized by its intracellular enzyme system to achieve degradation [118,119,120,121,122]. In addition, fungi can produce hydrophobins that adhere hyphae to plastic surfaces, and they can also penetrate the surface of the polymer material and move deep into it, which can degrade the matrix to the greatest extent possible [123]. Daly et al. [120] summarized the methods of fungal degradation of lignocellulose and proposed the feasibility of fungal degradation of plastics. This fungal degradation mechanism also exists in the degradation process of MPs. Table 2 summarizes the fungi currently capable of degrading MPs.
The animal body is also the habitat of fungi and a potential site for screening MP-degrading fungi. Zhang et al. [87] isolated the PE-degrading fungus Aspergillus flavus-PEDX3 from the intestinal contents of Galleria mellonella. After 28 days of mixed culture with HDPE, through Fourier transform infrared spectroscopy analysis, it was found that carbonyl and ether groups had appeared on the surface of HDPE, indicating that pedx3 could degrade MPs. In addition, two laccase-like multicopper oxidase (LMCO) genes, AFLA_006190 and AFLA_053930, were found to be upregulated during degradation by reverse transcription-polymerase chain reaction (RT-PCR). It was confirmed that fungi can degrade HDPE by secreting enzymes [87].
There are many types of microorganisms in the soil [124]. Landfills are the places where most waste plastics accumulate, resulting in many microorganisms that can degrade MPs, of which fungi are an important part. At present, many researchers have isolated fungi that can degrade MPs from landfills and have further studied their degradation effects on these MPs. Gajendiran et al. [125] studied the degradation of LDPE by Aspergillus clavatus-JASK1 isolated from a landfill soil, and after 90 days of culture, its weight loss reached 35%. Verma et al. [126] isolated two fungi, A. flavus and A. terreus, from the landfill in Agra, and after culturing them in soil and LDPE for 9 months, their weights decreased by 30.6% and 11.4%, respectively. After 4 months of mixed culture with LDPE in the liquid medium, their weights dropped by 14.3% and 13.1%, respectively. Balasubramanian et al. [127] isolated the fungus Aspergillus terreus MF12 from a plastic waste dump. Through weight loss and Fourier transform infrared spectroscopy analysis, it was found that the strain could effectively degrade HDPE, and after 30 days of culture, the HDPE lost 9.4% of its weight [127]. In addition, the effect of different environmental factors on the degradation process of HDPE was also studied in this experiment. Under optimal conditions, the degradation rate could reach up to 20.8% [127]. Kunlere et al. [128] reported that two fungi, Aspergillus flavus MCP5 and Aspergillus flavus MMP10, were able to grow using LDPE as carbon and nitrogen sources, and Fourier transform infrared spectroscopy showed changes in the functional groups of their samples. Compared with the control, the peak intensities of the other spectra were increased or decreased, indicating that the two fungi were able to participate in the degradation process of LDPE. Ameen et al. [129] isolated six fungi from the Saudi Arabian mangrove sediments. After co-cultivation with LDPE, examination under light and SEM revealed that a large number of fungi were attached to the surface, more lignin-decomposing enzymes were produced, and more CO2 was released. These observations suggest that the screened fungi can decompose and consume LDPE. In addition to screening landfills for MP-degrading fungi, fungal species capable of degrading MPs also exist in other soils. Russell et al. [130] isolated the fungus Pestalotiopsis microspora from Amazonian plant samples in Ecuador. Under aerobic and anaerobic conditions, the isolate was able to grow with a unique polyester polyurethane (PUR) as the sole carbon source, which could secrete serine hydrolases to degrade PUR.
Fungi that can utilize and decompose MPs also exist in the ocean. Paco et al. [131] studied the response of the marine fungus Zalerion maritimum to PE particles at different incubation times. The results showed that the fungus could utilize PE and reduce the size and quality of PE particles, and the removal rate of PE was as high as 43% on the 14th day of culture [131,132]. Devi et al. [133] isolated two fungal strains, Aspergillus tubingensis VRKPT1 and Aspergillus flavus VRKPT2, from PE waste near the coast, and the fungi could survive using native PE as a carbon source. After 30 days of culture, the weight of HDPE was reduced by 6.02% and 8.51%, respectively. Although there are few reports on the degradation of MPs by fungi, according to the analysis of the reported literature, fungi degrade MPs very efficiently, so it is imperative to screen more kinds of fungi in future research to reduce the impact of MPs on the environment.
Table 2. Research status of fungal degradation of MPs.
Table 2. Research status of fungal degradation of MPs.
Fungi TypeTypes
of MPs
Duration of
Degradation
Weight LossReferences
Aspergillus flavus PEDX3HDPE28 d3.9%[87]
Aspergillus clavatu JASK1LDPE90 d35%[125]
A. flavusLDPE120 d14.3%[126]
A. terreusLDPE120 d13.1%[126]
A. flavusLDPE270 d30.6%[126]
A. terreusLDPE270 d11.4%[126]
Aspergillus terreus MF12.HDPE30 d9.4%[127]
Aspergillus flavus MCP5LDPE14 d1.67%[128]
Alternaria alternata, Aspergillus caespitosus, Aspergillus terreus, Eupenicillium hirayamae, Paecilomyces variotii, and Phialophora albaLDPE28 d [129]
Pestalotiopsis microsporaPUR14 d [130]
Zalerion maritimumPE14 d43%[131]
Aspergillus tubingensis VRKPT1HDPE30 d6.02%[132]
Aspergillus flavus VRKPT2HDPE30 d8.51%[132]

3.4. Combined Degradation of MPs by Bacteria and Fungi

In terms of MP biodegradation, most previous research has focused on the isolation of a single class of microorganisms with degrading ability; however, studies have shown that the combination of bacteria and fungi has a more efficient degradation efficiency. Esmaeili et al. [134] isolated two strains with a significant ability to degrade LDPE from a landfill soil in Tehran: the bacterium Lysinibacillus xylanilyticus and the fungus Aspergillus niger F1. FTIR, XRD, and SEM analysis proved the degradation potential of the mixed bacteria using PE as a carbon source. After 126 days of treatment, the biodegradation of UV-irradiated and non-UV-irradiated films reached 29.5% and 15.8%, respectively [134].

4. Summary and Outlook

In the future, the production of plastic products will continue to exhibit an upward trend. Plastic pollution has become an ecological and environmental problem that cannot be ignored in the Earth’s biosphere. Plastics undergo physical, chemical, biological, and other forms of wear, consumption, and decomposition to produce MPs with smaller particle sizes, which have been proven to be ubiquitous in the environment. With the increasing seriousness of MP pollution, it is imperative to explore effective MP degradation methods. In this paper, for the first time, the current degradation technologies of MPs and their advantages and disadvantages are systematically reviewed. The degradation mechanism and efficiency of biodegradation processes are mainly introduced, and the high efficiency and sustainable development potential of biodegradation are emphasized, as are the prospects of large-scale biological applications in the future. This review described the degradation efficiency of MPs by different microorganisms, including 45 bacteria and 18 fungi. Some of these microorganisms used MPs as the only source of nutrient elements. Through this paper, it is found that the microbial removal process has the advantages of high efficiency, being environmentally friendly, low cost, and sustainability; it is the most effective, energy-saving, and applicable degradation method for future large-scale applications.
Based on the above summary, in order to reduce the harm of MPs and understand the feasibility of the biodegradation process, we provide several directions for future research. First, we can screen plants that can effectively absorb MPs in the soil to improve the soil environment. Second, screen for microorganisms, such as fungi and mixed flora, that can efficiently degrade MPs. Third, remediation of MPs-contaminated soil by inoculation with degrading bacteria. In conclusion, this paper provides a solution for the management of MPs, a reference for the sustainable development and large-scale application of microplastic degradation in the future, and a suggestion for environmental management and policymaking by governments around the world.

Author Contributions

Literature retrieval and information collection, P.X. and Q.L.; analyzed the data, T.Z. and Q.W.; wrote and reviewed the paper, Q.L. and P.X.; project management, Q.L. All authors have read and agreed to the published version of the manuscript.

Funding

This work is supported by Sichuan Natural Science Foundation Project (2023NSFSC1229) and Open Foundation of Hebei Key Laboratory of Wetland Ecology and Conservation (No. hklk202203).

Institutional Review Board Statement

This article does not contain any studies with human participants or animals performed by any of the authors.

Informed Consent Statement

Not applicable.

Data Availability Statement

All data analyzed during this study are included in this article.

Conflicts of Interest

The authors declare no competing interests.

Abbreviations

MPs: microplastics; NPs: nanoparticles; PS: polystyrene; PP: polypropylene; PE: polyethylene; PU: polyurethane; PC: polycarbonate; PHA: polyhydroxyalkanoates; PVC: polyvinyl chloride; PVA: polyvinyl alcohol; PET: polyethylene terephthalate; LDPE: low-density polyethylene; HDPE: high-density polyethylene; PVA-LLDPE: linear low-density polyethylene; AOPs: advanced oxidation process; HTC: high-temperature composting

References

  1. Sharuddin, S.; Abnisa, F.; Daud, W.; Aroua, M.K.J.E.C. A review on pyrolysis of plastic wastes. Energy Convers. Manag. 2016, 115, 308–326. [Google Scholar] [CrossRef]
  2. Boucher, J.; Friot, D. Primary Microplastics in the Oceans: A Global Evaluation of Sources; IUCN: Gland, Switzerland, 2017. [Google Scholar]
  3. Kawecki, D.; Scheeder, P.; Nowack, B. Probabilistic Material Flow Analysis of Seven Commodity Plastics in Europe. Environ. Sci. Technol. 2018, 52, 9874–9888. [Google Scholar] [CrossRef]
  4. Meng, Y.; Kelly, F.J.; Wright, S.L. Advances and challenges of microplastic pollution in freshwater ecosystems: A UK perspective. Environ. Pollut. 2020, 256, 113445. [Google Scholar] [CrossRef]
  5. Lebreton, L.; Andrady, A. Future scenarios of global plastic waste generation and disposal. Palgrave Commun. 2019, 5, 6. [Google Scholar] [CrossRef]
  6. Eerkes-Medrano, D.; Thompson, R.C.; Aldridge, D.C. Microplastics in freshwater systems: A review of the emerging threats, identification of knowledge gaps and prioritisation of research needs. Water Res. 2015, 75, 63–82. [Google Scholar] [CrossRef] [PubMed]
  7. Abel, D.; Kloas, W.; Zarfl, C.; Hempel, S.; Rillig, M.C. Microplastics as an emerging threat to terrestrial ecosystems. Glob. Chang. Biol. 2017, 24, 1405–1416. [Google Scholar]
  8. De-la-Torre, G.E.; Dioses-Salinas, D.C.; Pizarro-Ortega, C.I.; Santillan, L. New plastic formations in the Anthropocene. Sci. Total Environ. 2022, 754, 142216. [Google Scholar] [CrossRef]
  9. Xiang, P.; Zhang, Y.; Zhang, T.; Wu, Q.; Zhao, C.; Li, Q. A novel bacterial combination for efficient degradation of polystyrene microplastics. J. Hazard. Mater. 2023, 458, 131856. [Google Scholar] [CrossRef]
  10. Shen, M.C.; Song, B.; Zeng, G.M.; Zhang, Y.X.; Huang, W.; Wen, X.F.; Tang, W.W. Are biodegradable plastics a promising solution to solve the global plastic pollution? Environ. Pollut. 2020, 263, 114469. [Google Scholar] [CrossRef]
  11. Yurtsever, M. Glitters as a Source of Primary Microplastics: An Approach to Environmental Responsibility and Ethics. J. Agric. Environ. Ethics 2019, 32, 459–478. [Google Scholar] [CrossRef]
  12. Yurtsever, M. Tiny, shiny, and colorful microplastics: Are regular glitters a significant source of microplastics? Mar. Pollut. Bull. 2019, 146, 678–682. [Google Scholar] [CrossRef]
  13. Qu, H.; Ma, R.X.; Barrett, H.; Wang, B.; Han, J.J.; Wang, F.; Chen, P.; Wang, W.; Peng, G.L.; Yu, G. How microplastics affect chiral illicit drug methamphetamine in aquatic food chain? From green alga (Chlorella pyrenoidosa) to freshwater snail (Cipangopaludian cathayensis). Environ. Int. 2020, 136, 105480. [Google Scholar] [CrossRef] [PubMed]
  14. Ge, J.H.; Li, H.; Liu, P.; Zhang, Z.P.; Ouyang, Z.Z.; Guo, X.T. Review of the toxic effect of microplastics on terrestrial and aquatic plants. Sci. Total Environ. 2021, 791, 148333. [Google Scholar] [CrossRef] [PubMed]
  15. Mateos-Cardenas, A.; Scott, D.T.; Seitmaganbetova, G.; van Pelt, F.; O’Halloran, J.; Jansen, M.A.K. Polyethylene microplastics adhere to Lemna minor (L.), yet have no effects on plant growth or feeding by Gammarus duebeni (Lillj.). Sci. Total Environ. 2019, 689, 413–421. [Google Scholar] [CrossRef] [PubMed]
  16. Tanaka, K.; Watanuki, Y.; Takada, H.; Ishizuka, M.; Yamashita, R.; Kazama, M.; Hiki, N.; Kashiwada, F.; Mizukawa, K.; Mizukawa, H.; et al. In Vivo Accumulation of Plastic-Derived Chemicals into Seabird Tissues. Curr. Biol. 2020, 30, 723–728.e3. [Google Scholar] [CrossRef]
  17. Qiao, R.X.; Deng, Y.F.; Zhang, S.H.; Wolosker, M.B.; Zhu, Q.D.; Ren, H.Q.; Zhang, Y. Accumulation of different shapes of microplastics initiates intestinal injury and gut microbiota dysbiosis in the gut of zebrafish. Chemosphere 2019, 236, 124334. [Google Scholar] [CrossRef] [PubMed]
  18. Cho, Y.; Shim, W.J.; Jang, M.; Han, G.M.; Hong, S.H. Abundance and characteristics of microplastics in market bivalves from South Korea. Environ. Pollut. 2019, 245, 1107–1116. [Google Scholar] [CrossRef]
  19. Van Cauwenberghe, L.; Janssen, C.R. Microplastics in bivalves cultured for human consumption. Environ. Pollut. 2014, 193, 65–70. [Google Scholar] [CrossRef]
  20. Vroom, R.J.E.; Koelmans, A.A.; Besseling, E.; Halsband, C. Aging of microplastics promotes their ingestion by marine zooplankton. Environ. Pollut. 2017, 231, 987–996. [Google Scholar] [CrossRef]
  21. Sathicq, M.B.; Sabatino, R.; Corno, G.; Di Cesare, A. Are microplastic particles a hotspot for the spread and the persistence of antibiotic resistance in aquatic systems? Environ. Pollut. 2021, 279, 116896. [Google Scholar] [CrossRef]
  22. Naik, R.K.; Naik, M.M.; D’Costa, P.M.; Shaikh, F. Microplastics in ballast water as an emerging source and vector for harmful chemicals, antibiotics, metals, bacterial pathogens and HAB species: A potential risk to the marine environment and human health. Mar. Pollut. Bull. 2019, 149, 110525. [Google Scholar] [CrossRef]
  23. Sharma, M.D.; Elanjickal, A.I.; Mankar, J.S.; Krupadam, R.J. Assessment of cancer risk of microplastics enriched with polycyclic aromatic hydrocarbons. J. Hazard. Mater. 2020, 398, 122994. [Google Scholar] [CrossRef] [PubMed]
  24. Tien, C.J.; Wang, Z.X.; Chen, C.S. Microplastics in water, sediment and fish from the Fengshan River system: Relationship to aquatic factors and accumulation of polycyclic aromatic hydrocarbons by fish. Environ. Pollut. 2020, 265, 114962. [Google Scholar] [CrossRef] [PubMed]
  25. Xu, S.; Ma, J.; Ji, R.; Pan, K.; Miao, A.J. Microplastics in aquatic environments: Occurrence, accumulation, and biological effects. Sci. Total Environ. 2020, 703, 134699. [Google Scholar] [CrossRef] [PubMed]
  26. Tang, Y.Q.; Liu, Y.G.; Chen, Y.; Zhang, W.; Zhao, J.M.; He, S.Y.; Yang, C.P.; Zhang, T.; Tang, C.F.; Zhang, C.; et al. A review: Research progress on microplastic pollutants in aquatic environments. Sci. Total Environ. 2021, 766, 142572. [Google Scholar] [CrossRef] [PubMed]
  27. Huang, W.; Song, B.A.; Liang, J.; Niu, Q.Y.; Zeng, G.M.; Shen, M.C.; Deng, J.Q.; Luo, Y.A.; Wen, X.F.; Zhang, Y.F. Microplastics and associated contaminants in the aquatic environment: A review on their ecotoxicological effects, trophic transfer, and potential impacts to human health. J. Hazard. Mater. 2021, 405, 124187. [Google Scholar] [CrossRef] [PubMed]
  28. Rainieri, S.; Conlledo, N.; Larsen, B.K.; Granby, K.; Barranco, A. Combined effects of microplastics and chemical contaminants on the organ toxicity of zebrafish (Danio rerio). Environ. Res. 2018, 162, 135–143. [Google Scholar] [CrossRef]
  29. Rodrigues, J.P.; Duarte, A.C.; Santos-Echeandia, J.; Rocha-Santos, T. Significance of interactions between microplastics and POPs in the marine environment: A critical overview. Trac-Trends Anal. Chem. 2019, 111, 252–260. [Google Scholar] [CrossRef]
  30. Oberbeckmann, S.; Labrenz, M. Marine Microbial Assemblages on Microplastics: Diversity, Adaptation, and Role in Degradation. Annu. Rev. Mar. Sci. 2020, 12, 209–232. [Google Scholar] [CrossRef]
  31. Kesy, K.; Oberbeckmann, S.; Kreikemeyer, B.; Labrenz, M. Spatial Environmental Heterogeneity Determines Young Biofilm Assemblages on Microplastics in Baltic Sea Mesocosms. Front. Microbiol. 2019, 10, 1665. [Google Scholar] [CrossRef]
  32. Stabnikova, O.; Stabnikov, V.; Marinin, A.; Klavins, M.; Klavins, L.; Vaseashta, A. Microbial Life on the Surface of Microplastics in Natural Waters. Appl. Sci. 2021, 11, 11692. [Google Scholar] [CrossRef]
  33. Zhang, F.; Zhao, Y.T.; Wang, D.D.; Yan, M.Q.; Zhang, J.; Zhang, P.Y.; Ding, T.G.; Chen, L.; Chen, C. Current technologies for plastic waste treatment: A review. J. Clean. Prod. 2021, 282, 124523. [Google Scholar] [CrossRef]
  34. Bao, Z.; Feng, H.; Tu, W.; Li, L.; Li, Q. Method and mechanism of chromium removal from soil: A systematic review. Environ. Sci. Pollut. Res. Int. 2022, 29, 35501–35517. [Google Scholar] [CrossRef] [PubMed]
  35. Du, H.; Xie, Y.Q.; Wang, J. Microplastic degradation methods and corresponding degradation mechanism: Research status and future perspectives. J. Hazard. Mater. 2021, 418, 126377. [Google Scholar] [CrossRef]
  36. Li, L.; Xu, W.; Tan, Y.; Yang, Y.; Yang, J.; Tan, D. Fluid-induced vibration evolution mechanism of multiphase free sink vortex and the multi-source vibration sensing method. Mech. Syst. Signal Process. 2023, 189, 110058. [Google Scholar] [CrossRef]
  37. Zhu, K.C.; Jia, H.Z.; Sun, Y.J.; Dai, Y.C.; Zhang, C.; Guo, X.T.; Wang, T.C.; Zhu, L.Y. Long-term phototransformation of microplastics under simulated sunlight irradiation in aquatic environments: Roles of reactive oxygen species. Water Res. 2020, 173, 115564. [Google Scholar] [CrossRef]
  38. Xu, L.; Crawford, K.; Gorman, C.B. Effects of Temperature and pH on the Degradation of Poly(lactic acid) Brushes. Macromolecules 2011, 44, 4777–4782. [Google Scholar] [CrossRef]
  39. Anand, U.; Dey, S.; Bontempi, E.; Ducoli, S.; Vethaak, A.D.; Dey, A.; Federici, S. Biotechnological methods to remove microplastics: A review. Environ. Chem. Lett. 2023, 21, 1787–1810. [Google Scholar] [CrossRef]
  40. Gaylarde, C.C.; Neto, J.A.B.; da Fonseca, E.M. Nanoplastics in aquatic systems—Are they more hazardous than microplastics? Environ. Pollut. 2021, 272, 115950. [Google Scholar] [CrossRef]
  41. Li, L.; Gu, Z.; Xu, W.; Tan, Y.; Fan, X.; Tan, D. Mixing mass transfer mechanism and dynamic control of gas-liquid-solid multiphase flow based on VOF-DEM coupling. Energy 2023, 272, 127015. [Google Scholar] [CrossRef]
  42. Lin, L.; Bin, L.; Wei-xin, X.; Ze-heng, G.; Yuan-shan, Y.; Da-peng, T. Multiphase coupling transport evolution mechanism of the free sink vortex. Acta Phys. Sin. 2023, 72, 034702. [Google Scholar] [CrossRef]
  43. Herbort, A.F.; Sturm, M.T.; Schuhen, K. A new approach for the agglomeration and subsequent removal of polyethylene, polypropylene, and mixtures of both from freshwater systems—A case study. Environ. Sci. Pollut. Res. 2018, 25, 15226–15234. [Google Scholar] [CrossRef]
  44. Leppänen, I.; Lappalainen, T.; Lohtander, T.; Jonkergouw, C.; Arola, S.; Tammelin, T. Capturing colloidal nano- and microplastics with plant-based nanocellulose networks. Nat. Commun. 2022, 13, 1814. [Google Scholar] [CrossRef]
  45. Choudhary, M.; Kumar, R.; Neogi, S. Activated biochar derived from Opuntia ficus-indica for the efficient adsorption of malachite green dye, Cu+2 and Ni+2 from water. J. Hazard. Mater. 2020, 392, 122441. [Google Scholar] [CrossRef]
  46. Regkouzas, P.; Diamadopoulos, E. Adsorption of selected organic micro-pollutants on sewage sludge biochar. Chemosphere 2019, 224, 840–851. [Google Scholar] [CrossRef]
  47. Wang, J.; Sun, C.; Huang, Q.X.; Chi, Y.; Yan, J.H. Adsorption and thermal degradation of microplastics from aqueous solutions by Mg/Zn modified magnetic biochars. J. Hazard. Mater. 2021, 419, 126486. [Google Scholar] [CrossRef]
  48. Tiwari, E.; Singh, N.; Khandelwal, N.; Monikh, F.A.; Darbha, G.K. Application of Zn/Al layered double hydroxides for the removal of nanoscale plastic debris from aqueous systems. J. Hazard. Mater. 2020, 397, 122769. [Google Scholar] [CrossRef]
  49. Sun, C.Z.; Wang, Z.G.; Chen, L.Y.; Li, F.M. Fabrication of robust and compressive chitin and graphene oxide sponges for removal of microplastics with different functional groups. Chem. Eng. J. 2020, 393, 124796. [Google Scholar] [CrossRef]
  50. Sharma, S.; Basu, S.; Shetti, N.P.; Nadagouda, M.N.; Aminabhavi, T.M. Microplastics in the environment: Occurrence, perils, and eradication. Chem. Eng. J. 2021, 408, 127317. [Google Scholar] [CrossRef]
  51. Chen, J.L.; Wu, J.; Sherrell, P.C.; Chen, J.; Wang, H.P.; Zhang, W.X.; Yang, J.P. How to Build a Microplastics-Free Environment: Strategies for Microplastics Degradation and Plastics Recycling. Adv. Sci. 2022, 9, 2103764. [Google Scholar] [CrossRef]
  52. Ricardo, I.A.; Alberto, E.A.; Silva, A.H.; Macuvele, D.; Padoin, N.; Soares, C.; Riella, H.G.; Starling, M.; Trovo, A.G. A critical review on microplastics, interaction with organic and inorganic pollutants, impacts and effectiveness of advanced oxidation processes applied for their removal from aqueous matrices. Chem. Eng. J. 2021, 424, 130282. [Google Scholar] [CrossRef]
  53. Hu, W.; Liu, D.D.; Su, S.H.; Ren, L.J.; Ren, H.; Wei, L.F.; Yue, S.Y.; Xie, Q.R.; Zhang, Z.M.; Wang, Z.H.; et al. Photochemical Degradation of Organic Matter in the Atmosphere. Adv. Sustain. Syst. 2021, 5, 2100027. [Google Scholar] [CrossRef]
  54. Liu, P.; Qian, L.; Wang, H.Y.; Zhan, X.; Lu, K.; Gu, C.; Gao, S.X. New Insights into the Aging Behavior of Microplastics Accelerated by Advanced Oxidation Processes. Environ. Sci. Technol. 2019, 53, 3579–3588. [Google Scholar] [CrossRef] [PubMed]
  55. Cai, L.Q.; Wang, J.D.; Peng, J.P.; Wu, Z.Q.; Tan, X.L. Observation of the degradation of three types of plastic pellets exposed to UV irradiation in three different environments. Sci. Total Environ. 2018, 628–629, 740–747. [Google Scholar] [CrossRef] [PubMed]
  56. Zhu, K.C.; Jia, H.Z.; Zhao, S.; Xia, T.J.; Guo, X.T.; Wang, T.C.; Zhu, L.Y. Formation of Environmentally Persistent Free Radicals on Microplastics under Light Irradiation. Environ. Sci. Technol. 2019, 53, 8177–8186. [Google Scholar] [CrossRef] [PubMed]
  57. Wu, N.N.; Cao, W.M.; Qu, R.J.; Zhou, D.M.; Sun, C.; Wang, Z.Y. Photochemical transformation of decachlorobiphenyl (PCB-209) on the surface of microplastics in aqueous solution. Chem. Eng. J. 2021, 420, 129813. [Google Scholar] [CrossRef]
  58. Ainali, N.M.; Bikiaris, D.N.; Lambropoulou, D.A. Aging effects on low- and high-density polyethylene, polypropylene and polystyrene under UV irradiation: An insight into decomposition mechanism by Py-GC/MS for microplastic analysis. J. Anal. Appl. Pyrolysis 2021, 158, 105207. [Google Scholar] [CrossRef]
  59. Ding, L.; Ouyang, Z.Z.; Liu, P.; Wang, T.C.; Jia, H.Z.; Guo, X.T. Photodegradation of microplastics mediated by different types of soil: The effect of soil components. Sci. Total Environ. 2022, 802, 149840. [Google Scholar] [CrossRef]
  60. Wang, C.; Xian, Z.; Jin, X.; Liang, S.; Chen, Z.; Pan, B.; Wu, B.; Ok, Y.S.; Gu, C. Photo-aging of polyvinyl chloride microplastic in the presence of natural organic acids. Water Res. 2020, 183, 116082. [Google Scholar] [CrossRef]
  61. Zhang, X.L.; Xia, M.L.; Su, X.J.; Yuan, P.; Li, X.K.; Zhou, C.Y.; Wan, Z.P.; Zou, W. Photolytic degradation elevated the toxicity of polylactic acid microplastics to developing zebrafish by triggering mitochondrial dysfunction and apoptosis. J. Hazard. Mater. 2021, 413, 125321. [Google Scholar] [CrossRef]
  62. Wang, X.; Zheng, H.; Zhao, J.; Luo, X.X.; Zhenyu, W.; Xing, B.S. Photodegradation Elevated the Toxicity of Polystyrene Microplastics to Grouper (Epinephelus moara) through Disrupting Hepatic Lipid Homeostasis. Environ. Sci. Technol. 2020, 54, 6202–6212. [Google Scholar] [CrossRef]
  63. Chen, H.B.; Yang, Y.; Wang, C.; Hua, X.; Li, H.; Xie, D.L.; Xiang, M.D.; Yu, Y.J. Reproductive toxicity of UV-photodegraded polystyrene microplastics induced by DNA damage-dependent cell apoptosis in Caenorhabditis elegans. Sci. Total Environ. 2022, 811, 152350. [Google Scholar] [CrossRef]
  64. Addanki Tirumala, R.T. Exploiting the Optical Properties of Earth Abundant Cuprous Oxide Nanocatalysts for Energy and Health Applications. Ph.D. Thesis, Oklahoma State University, Stillwater, OK, USA, 2022. [Google Scholar]
  65. Li, L.; Tan, Y.; Xu, W.; Ni, Y.; Yang, J.; Tan, D. Fluid-induced transport dynamics and vibration patterns of multiphase vortex in the critical transition states. Int. J. Mech. Sci. 2023, 252, 108376. [Google Scholar] [CrossRef]
  66. Kwon, Y.T.; Lim, G.D.; Kim, S.; Ryu, S.H.; Hwang, T.Y.; Park, K.R.; Choa, Y.H. Near-infrared absorbance properties of Cu2-xS/SiO2 nanoparticles and their PDMS-based composites. J. Mater. Chem. C 2018, 6, 754–760. [Google Scholar] [CrossRef]
  67. Tofa, T.S.; Kunjali, K.L.; Paul, S.; Dutta, J. Visible light photocatalytic degradation of microplastic residues with zinc oxide nanorods. Environ. Chem. Lett. 2019, 17, 1341–1346. [Google Scholar] [CrossRef]
  68. Nabi, I.; Bacha, A.U.R.; Li, K.J.; Cheng, H.Y.; Wang, T.; Liu, Y.Y.; Ajmal, S.; Yang, Y.; Feng, Y.Q.; Zhang, L.W. Complete Photocatalytic Mineralization of Microplastic on TiO2 Nanoparticle Film. Iscience 2020, 23, 101326. [Google Scholar] [CrossRef]
  69. Luo, H.W.; Xiang, Y.H.; Tian, T.; Pan, X.L. An AFM-IR study on surface properties of nano-TiO2 coated polyethylene (PE) thin film as influenced by photocatalytic aging process. Sci. Total Environ. 2021, 757, 143900. [Google Scholar] [CrossRef]
  70. Tofa, T.S.; Ye, F.; Kunjali, K.L.; Dutta, J. Enhanced Visible Light Photodegradation of Microplastic Fragments with Plasmonic Platinum/Zinc Oxide Nanorod Photocatalysts. Catalysts 2019, 9, 819. [Google Scholar] [CrossRef]
  71. Cao, B.Q.; Wan, S.P.; Wang, Y.A.; Guo, H.W.; Ou, M.; Zhong, Q. Highly-efficient visible-light-driven photocatalytic H2 evolution integrated with microplastic degradation over MXene/ZnxCd1-xS photocatalyst. J. Colloid. Interface Sci. 2022, 605, 311–319. [Google Scholar] [CrossRef]
  72. Zhou, X.S.; Jin, B.; Luo, J.; Gu, X.X.; Zhang, S.Q. Photoreduction preparation of Cu2O@polydopamine nanospheres with enhanced photocatalytic activity under visible light irradiation. J. Solid. State Chem. 2017, 254, 55–61. [Google Scholar] [CrossRef]
  73. Zhu, B.J.; Jiang, G.F.; Lv, Y.; Liu, F.; Sun, J. Photocatalytic degradation of polyacrylamide by rGO@Fe3O4/Cu2O@ZnO magnetic recyclable composites. Mater. Sci. Semicond. Process. 2021, 131, 105841. [Google Scholar] [CrossRef]
  74. Pary, F.F.; Addanki Tirumala, R.T.; Andiappan, M.; Nelson, T.L. Copper(i) oxide nanoparticle-mediated C-C couplings for synthesis of polyphenylenediethynylenes: Evidence for a homogeneous catalytic pathway. Catal. Sci. Technol. 2021, 11, 2414–2421. [Google Scholar] [CrossRef]
  75. Tirumala, R.T.A.; Gyawali, S.; Wheeler, A.; Ramakrishnan, S.B.; Sooriyagoda, R.; Mohammadparast, F.; Khatri, N.; Tan, S.; Kalkan, A.K.; Bristow, A.D.; et al. Structure–Property–Performance Relationships of Cuprous Oxide Nanostructures for Dielectric Mie Resonance-Enhanced Photocatalysis. ACS Catal. 2022, 12, 7975–7985. [Google Scholar] [CrossRef]
  76. Zhang, T.Y.; Liu, J.D.; Zhou, F.; Zhou, S.Y.; Wu, J.C.; Chen, D.Y.; Xu, Q.F.; Lu, J.M. Polymer-Coated Fe2O3 Nanoparticles for Photocatalytic Degradation of Organic Materials and Antibiotics in Water. Acs Appl. Nano Mater. 2020, 3, 9200–9208. [Google Scholar] [CrossRef]
  77. Zhang, X.Q.; Xia, L.; Liu, C.; Cheng, X.B.; Yang, Z. A direct Z-scheme heterojunction g-C3N4/alpha-Fe2O3 nanocomposite for enhanced polymer-containing oilfield sewage degradation under visible light. Environ. Sci.-Water Res. Technol. 2022, 8, 1965–1975. [Google Scholar] [CrossRef]
  78. Yin, X.N.; Wang, J.; Zhou, J.J.; Li, L. Mussel-inspired modification of Microporous polypropylene membranes for functional catalytic degradation. Chin. J. Polym. Sci. 2015, 33, 1721–1729. [Google Scholar] [CrossRef]
  79. Xu, X.X.; Cui, Z.P.; Qi, J.; Liu, X.X. Fabrication of Ag/CPs composite material, an effective strategy to improve the photocatalytic performance of coordination polymers under visible irradiation. Dalton Trans. 2013, 42, 13546–13553. [Google Scholar] [CrossRef]
  80. Xu, C.Y.; Chen, W.Q.; Wang, J.J.; Wu, Q.Y.; Wu, P.Y.; Tang, L. Two Cu(I\II) Coordination Polymers for Photocatalytic Degradation of Organic Dyes and Efficient Detection of Fe3+ Ions. J. Inorg. Organomet. Polym. Mater. 2023, 33, 885–894. [Google Scholar] [CrossRef]
  81. Miao, F.; Liu, Y.F.; Gao, M.M.; Yu, X.; Xiao, P.W.; Wang, M.; Wang, S.G.; Wang, X.H. Degradation of polyvinyl chloride microplastics via an electro-Fenton-like system with a TiO2/graphite cathode. J. Hazard. Mater. 2020, 399, 123023. [Google Scholar] [CrossRef]
  82. Krueger, M.C.; Harms, H.; Schlosser, D. Prospects for microbiological solutions to environmental pollution with plastics. Appl. Microbiol. Biotechnol. 2015, 99, 8857–8874. [Google Scholar] [CrossRef]
  83. Yang, S.S.; Wu, W.M.; Brandon, A.M.; Fan, H.Q.; Receveur, J.P.; Li, Y.R.; Wang, Z.Y.; Fan, R.; McClellan, R.L.; Gao, S.H.; et al. Ubiquity of polystyrene digestion and biodegradation within yellow mealworms, larvae of Tenebrio molitor Linnaeus (Coleoptera: Tenebrionidae). Chemosphere 2018, 212, 262–271. [Google Scholar] [CrossRef] [PubMed]
  84. Baeza, C.; Cifuentes, C.; Gonzalez, P.; Araneda, A.; Barra, R. Experimental Exposure of Lumbricus terrestristo Microplastics. Water Air Soil. Pollut. 2020, 231, 308. [Google Scholar] [CrossRef]
  85. Song, Y.; Qiu, R.; Hu, J.N.; Li, X.Y.; Zhang, X.T.; Chen, Y.X.; Wu, W.M.; He, D.F. Biodegradation and disintegration of expanded polystyrene by land snails Achatina fulica. Sci. Total Environ. 2020, 746, 141289. [Google Scholar] [CrossRef] [PubMed]
  86. Billen, P.; Khalifa, L.; Van Gerven, F.; Tavernier, S.; Spatari, S. Technological application potential of polyethylene and polystyrene biodegradation by macro -organisms such as mealworms and wax moth larvae. Sci. Total Environ. 2020, 735, 139521. [Google Scholar] [CrossRef]
  87. Zhang, J.Q.; Gao, D.L.; Li, Q.H.; Zhao, Y.X.; Li, L.; Lin, H.F.; Bi, Q.R.; Zhao, Y.C. Biodegradation of polyethylene microplastic particles by the fungus Aspergillus flavus from the guts of wax moth Galleria mellonella. Sci. Total Environ. 2020, 704, 135931. [Google Scholar] [CrossRef]
  88. Luo, L.P.; Wang, Y.M.; Guo, H.Q.; Yang, Y.H.; Qi, N.; Zhao, X.; Gao, S.H.; Zhou, A.F. Biodegradation of foam plastics by Zophobas atratus larvae (Coleoptera: Tenebrionidae) associated with changes of gut digestive enzymes activities and microbiome. Chemosphere 2021, 282, 131006. [Google Scholar] [CrossRef]
  89. Ali, S.S.; Elsamahy, T.; Koutra, E.; Kornaros, M.; El-Sheekh, M.; Abdelkarim, E.A.; Zhu, D.C.; Sun, J.Z. Degradation of conventional plastic wastes in the environment: A review on current status of knowledge and future perspectives of disposal. Sci. Total Environ. 2021, 771, 144719. [Google Scholar] [CrossRef]
  90. Othman, A.R.; Abu Hasan, H.; Muhamad, M.H.; Ismail, N.I.; Abdullah, S.R.S. Microbial degradation of microplastics by enzymatic processes: A review. Environ. Chem. Lett. 2021, 19, 3057–3073. [Google Scholar] [CrossRef]
  91. Ali, S.S.; Elsamahy, T.; Al-Tohamy, R.; Zhu, D.C.; Mahmoud, Y.A.G.; Koutra, E.; Metwally, M.A.; Kornaros, M.; Sun, J.Z. Plastic wastes biodegradation: Mechanisms, challenges and future prospects. Sci. Total Environ. 2021, 780, 146590. [Google Scholar] [CrossRef]
  92. Yuan, J.H.; Ma, J.; Sun, Y.R.; Zhou, T.; Zhao, Y.C.; Yu, F. Microbial degradation and other environmental aspects of microplastics/plastics. Sci. Total Environ. 2020, 715, 136968. [Google Scholar] [CrossRef]
  93. Yin, C.F.; Xu, Y.; Zhou, N.Y. Biodegradation of polyethylene mulching films by a co-culture of Acinetobacter sp. strain NyZ450 and Bacillus sp. strain NyZ451 isolated from Tenebrio molitor larvae. Int. Biodeterior. Biodegrad. 2020, 155, 105089. [Google Scholar] [CrossRef]
  94. Yang, Y.; Yang, J.; Wu, W.M.; Zhao, J.; Song, Y.L.; Gao, L.C.; Yang, R.F.; Jiang, L. Biodegradation and Mineralization of Polystyrene by Plastic-Eating Mealworms: Part 2. Role of Gut Microorganisms. Environ. Sci. Technol. 2015, 49, 12087–12093. [Google Scholar] [CrossRef] [PubMed]
  95. Lwanga, E.H.; Thapa, B.; Yang, X.M.; Gertsen, H.; Salanki, T.; Geissen, V.; Garbeva, P. Decay of low-density polyethylene by bacteria extracted from earthworm’s guts: A potential for soil restoration. Sci. Total Environ. 2018, 624, 753–757. [Google Scholar] [CrossRef]
  96. Vimala, P.P.; Mathew, L. Biodegradation of Polyethylene Using Bacillus Subtilis. Procedia Technol. 2016, 24, 232–239. [Google Scholar] [CrossRef]
  97. Park, S.Y.; Kim, C.G. Biodegradation of micro-polyethylene particles by bacterial colonization of a mixed microbial consortium isolated from a landfill site. Chemosphere 2019, 222, 527–533. [Google Scholar] [CrossRef] [PubMed]
  98. Auta, H.S.; Emenike, C.U.; Fauziah, S.H. Screening of Bacillus strains isolated from mangrove ecosystems in Peninsular Malaysia for microplastic degradation. Environ. Pollut. 2017, 231, 1552–1559. [Google Scholar] [CrossRef]
  99. Auta, H.S.; Abioye, O.P.; Aransiola, S.A.; Bala, J.D.; Chukwuemeka, V.I.; Hassan, A.; Aziz, A.; Fauziah, S.H. Enhanced microbial degradation of PET and PS microplastics under natural conditions in mangrove environment. J. Environ. Manag. 2022, 304, 114273. [Google Scholar] [CrossRef]
  100. Auta, H.S.; Emenike, C.U.; Jayanthi, B.; Fauziah, S.H. Growth kinetics and biodeterioration of polypropylene microplastics by Bacillus sp. and Rhodococcus sp. isolated from mangrove sediment. Mar. Pollut. Bull. 2018, 127, 15–21. [Google Scholar] [CrossRef]
  101. Tu, W.; Cao, X.; Cheng, J.; Li, L.; Zhang, T.; Wu, Q.; Xiang, P.; Shen, C.; Li, Q. Chinese Baijiu: The Perfect Works of Microorganisms. Front. Microbiol. 2022, 13, 919044. [Google Scholar] [CrossRef]
  102. Wu, Q.; Li, L.; Xiang, P.; Zhang, T.; Peng, L.; Zou, L.; Li, Q. Phages in Fermented Foods: Interactions and Applications. Fermentation 2023, 9, 201. [Google Scholar] [CrossRef]
  103. Sun, Y.; Ren, X.N.; Rene, E.R.; Wang, Z.; Zhou, L.N.; Zhang, Z.Q.; Wang, Q. The degradation performance of different microplastics and their effect on microbial community during composting process. Bioresour. Technol. 2021, 332, 125133. [Google Scholar] [CrossRef]
  104. Chen, Z.; Zhao, W.Q.; Xing, R.Z.; Xie, S.J.; Yang, X.G.; Cui, P.; Lu, J.; Liao, H.P.; Yu, Z.; Wang, S.H.; et al. Enhanced in situ biodegradation of microplastics in sewage sludge using hyperthermophilic composting technology. J. Hazard. Mater. 2020, 384, 121271. [Google Scholar] [CrossRef]
  105. Bao, Z.; Wang, X.; Wang, Q.; Zou, L.; Peng, L.; Li, L.; Tu, W.; Li, Q. A novel method of domestication combined with ARTP to improve the reduction ability of Bacillus velezensis to Cr(VI). J. Environ. Chem. Eng. 2023, 11, 109091. [Google Scholar] [CrossRef]
  106. Skariyachan, S.; Patil, A.A.; Shankar, A.; Manjunath, M.; Bachappanavar, N.; Kiran, S. Enhanced polymer degradation of polyethylene and polypropylene by novel thermophilic consortia of Brevibacillus sps. and Aneurinibacillus sp. screened from waste management landfills and sewage treatment plants. Polym. Degrad. Stab. 2018, 149, 52–68. [Google Scholar] [CrossRef]
  107. Habib, S.; Iruthayam, A.; Abd Shukor, M.Y.; Alias, S.A.; Smykla, J.; Yasid, N.A. Biodeterioration of Untreated Polypropylene Microplastic Particles by Antarctic Bacteria. Polymers 2020, 12, 2616. [Google Scholar] [CrossRef] [PubMed]
  108. Grgic, D.K.; Miloloza, M.; Lovrincic, E.; Kovacevic, A.; Cvetnic, M.; Bulatovic, V.O.; Prevaric, V.; Bule, K.; Ukic, S.; Markic, M.; et al. Bioremediation of MP-polluted Waters Using Bacteria Bacillus licheniformis, Lysinibacillus massiliensis, and Mixed Culture of Bacillus sp. and Delftia acidovorans. Chem. Biochem. Eng. Q. 2021, 35, 205–224. [Google Scholar] [CrossRef]
  109. Devi, K.N.; Raju, P.; Santhanam, P.; Kumar, S.D.; Krishnaveni, N.; Roopavathy, J.; Perumal, P. Biodegradation of low-density polyethylene and polypropylene by microbes isolated from Vaigai River, Madurai, India. Arch. Microbiol. 2021, 203, 6253–6265. [Google Scholar] [CrossRef]
  110. Li, Z.Y.; Wei, R.; Gao, M.X.; Ren, Y.R.; Yu, B.; Nie, K.L.; Xu, H.J.; Liu, L. Biodegradation of low-density polyethylene by Microbulbifer hydrolyticus IRE-31. J. Environ. Manag. 2020, 263, 110402. [Google Scholar] [CrossRef] [PubMed]
  111. Giacomucci, L.; Raddadi, N.; Soccio, M.; Lotti, N.; Fava, F. Biodegradation of polyvinyl chloride plastic films by enriched anaerobic marine consortia. Mar. Environ. Res. 2020, 158, 104949. [Google Scholar] [CrossRef]
  112. Harshvardhan, K.; Jha, B. Biodegradation of low-density polyethylene by marine bacteria from pelagic waters, Arabian Sea, India. Mar. Pollut. Bull. 2013, 77, 100–106. [Google Scholar] [CrossRef] [PubMed]
  113. Raghul, S.S.; Bhat, S.G.; Chandrasekaran, M.; Francis, V.; Thachil, E.T. Biodegradation of polyvinyl alcohol-low linear density polyethylene-blended plastic film by consortium of marine benthic vibrios. Int. J. Environ. Sci. Technol. 2014, 11, 1827–1834. [Google Scholar] [CrossRef]
  114. Gao, R.R.; Sun, C.M. A marine bacterial community capable of degrading poly(ethylene terephthalate) and polyethylene. J. Hazard. Mater. 2021, 416, 125928. [Google Scholar] [CrossRef] [PubMed]
  115. Li, Q.; Xiang, P.; Li, L.; Zhang, T.; Wu, Q.; Bao, Z.; Tu, W.; Zhao, C. Phosphorus mining activities alter endophytic bacterial communities and metabolic functions of surrounding vegetables and crops. Plant Soil. 2023. [Google Scholar] [CrossRef]
  116. Li, Q.; Xiang, P.; Zhang, T.; Wu, Q.; Bao, Z.; Tu, W.; Li, L.; Zhao, C. The effect of phosphate mining activities on rhizosphere bacterial communities of surrounding vegetables and crops. Sci. Total Environ. 2022, 821, 153479. [Google Scholar] [CrossRef]
  117. Mitik-Dineva, N.; Wang, J.; Truong, V.K.; Stoddart, P.; Malherbe, F.; Crawford, R.J.; Ivanova, E.P. Escherichia coli, Pseudomonas aeruginosa, and Staphylococcus aureus Attachment Patterns on Glass Surfaces with Nanoscale Roughness. Curr. Microbiol. 2009, 58, 268–273. [Google Scholar] [CrossRef]
  118. Skariyachan, S.; Prasanna, A.; Manjunath, S.P.; Karanth, S.S.; Nazre, A. Environmental assessment of the degradation potential of mushroom fruit bodies of Pleurotus ostreatus (Jacq.: Fr.) P. Kumm. towards synthetic azo dyes and contaminating effluents collected from textile industries in Karnataka, India. Environ. Monit. Assess. 2016, 188, 121. [Google Scholar] [CrossRef]
  119. Ali, S.S.; Al-Tohamy, R.; Koutra, E.; Kornaros, M.; Khalil, M.; Elsamahy, T.; El-Shetehy, M.; Sun, J.Z. Coupling azo dye degradation and biodiesel production by manganese-dependent peroxidase producing oleaginous yeasts isolated from wood-feeding termite gut symbionts. Biotechnol. Biofuels 2021, 14, 61. [Google Scholar] [CrossRef]
  120. Daly, P.; Cai, F.; Kubicek, C.P.; Jiang, S.Q.; Grujic, M.; Rahimi, M.J.; Sheteiwy, M.S.; Giles, R.; Riaz, A.; de Vries, R.P.; et al. From lignocellulose to plastics: Knowledge transfer on the degradation approaches by fungi. Biotechnol. Adv. 2021, 50, 107770. [Google Scholar] [CrossRef]
  121. Wei, R.; Zimmermann, W. Microbial enzymes for the recycling of recalcitrant petroleum-based plastics: How far are we? Microb. Biotechnol. 2017, 10, 1308–1322. [Google Scholar] [CrossRef]
  122. Ali, S.S.; Al-Tohamy, R.; Koutra, E.; El-Naggar, A.H.; Kornaros, M.; Sun, J.Z. Valorizing lignin-like dyes and textile dyeing wastewater by a newly constructed lipid-producing and lignin modifying oleaginous yeast consortium valued for biodiesel and bioremediation. J. Hazard. Mater. 2021, 403, 123575. [Google Scholar] [CrossRef]
  123. Sanchez, C. Fungal potential for the degradation of petroleum-based polymers: An overview of macro- and microplastics biodegradation. Biotechnol. Adv. 2020, 40, 107501. [Google Scholar] [CrossRef] [PubMed]
  124. Zhang, T.; Qi, M.; Wu, Q.; Xiang, P.; Tang, D.; Li, Q. Recent research progress on the synthesis and biological effects of selenium nanoparticles. Front. Nutr. 2023, 10, 1183487. [Google Scholar] [CrossRef] [PubMed]
  125. Gajendiran, A.; Krishnamoorthy, S.; Abraham, J. Microbial degradation of low-density polyethylene (LDPE) by Aspergillus clavatus strain JASK1 isolated from landfill soil. 3 Biotech. 2016, 6, 52. [Google Scholar] [CrossRef] [PubMed]
  126. Verma, N.; Gupta, S. Assessment of LDPE degrading potential Aspergillus species isolated from municipal landfill sites of Agra. SN Appl. Sci. 2019, 1, 701. [Google Scholar] [CrossRef]
  127. Balasubramanian, V.; Natarajan, K.; Rajeshkannan, V.; Perumal, P. Enhancement of in vitro high-density polyethylene (HDPE) degradation by physical, chemical, and biological treatments. Environ. Sci. Pollut. Res. 2014, 21, 12549–12562. [Google Scholar] [CrossRef]
  128. Kunlere, I.O.; Fagade, O.E.; Nwadike, B.I. Biodegradation of low density polyethylene (LDPE) by certain indigenous bacteria and fungi. Int. J. Environ. Stud. 2019, 76, 428–440. [Google Scholar] [CrossRef]
  129. Ameen, F.; Moslem, M.; Hadi, S.; Al-Sabri, A.E. Biodegradation of Low Density Polyethylene (LDPE) by Mangrove Fungi From the Red Sea Coast. Prog. Rubber Plast. Recycl. Technol. 2015, 31, 125–144. [Google Scholar] [CrossRef]
  130. Russell, J.R.; Huang, J.; Anand, P.; Kucera, K.; Sandoval, A.G.; Dantzler, K.W.; Hickman, D.; Jee, J.; Kimovec, F.M.; Koppstein, D.; et al. Biodegradation of Polyester Polyurethane by Endophytic Fungi. Appl. Environ. Microbiol. 2011, 77, 6076–6084. [Google Scholar] [CrossRef]
  131. Paco, A.; Duarte, K.; da Costa, J.P.; Santos, P.S.M.; Pereira, R.; Pereira, M.E.; Freitas, A.C.; Duarte, A.C.; Rocha-Santos, T.A.P. Biodegradation of polyethylene microplastics by the marine fungus Zalerion maritimum. Sci. Total Environ. 2017, 586, 10–15. [Google Scholar] [CrossRef]
  132. Li, Q.; Luo, Y.; Sha, A.; Xiao, W.; Xiong, Z.; Chen, X.; He, J.; Peng, L.; Zou, L. Analysis of synonymous codon usage patterns in mitochondrial genomes of nine Amanita species. Front. Microbiol. 2023, 8, 1134228. [Google Scholar] [CrossRef]
  133. Devi, R.S.; Kannan, V.R.; Nivas, D.; Kannan, K.; Chandru, S.; Antony, A.R. Biodegradation of HDPE by Aspergillus spp. from marine ecosystem of Gulf of Mannar, India. Mar. Pollut. Bull. 2015, 96, 32–40. [Google Scholar] [CrossRef] [PubMed]
  134. Esmaeili, A.; Pourbabaee, A.A.; Alikhani, H.A.; Shabani, F.; Esmaeili, E. Biodegradation of Low-Density Polyethylene (LDPE) by Mixed Culture of Lysinibacillus xylanilyticus and Aspergillus niger in Soil. PLoS ONE 2013, 8, e71720. [Google Scholar] [CrossRef] [PubMed]
Figure 1. Source and migration characteristics of soil microplastics (MPs).
Figure 1. Source and migration characteristics of soil microplastics (MPs).
Sustainability 15 12698 g001
Figure 2. Absorption and transport of microplastics (MPs) in terrestrial plants. Arrows indicate microplastics absorbed by plants.
Figure 2. Absorption and transport of microplastics (MPs) in terrestrial plants. Arrows indicate microplastics absorbed by plants.
Sustainability 15 12698 g002
Figure 3. Pathways for animal decomposition of microplastics (MPs).
Figure 3. Pathways for animal decomposition of microplastics (MPs).
Sustainability 15 12698 g003
Figure 4. Pathways of bacteria- and fungi-degrading microplastics (MPs).
Figure 4. Pathways of bacteria- and fungi-degrading microplastics (MPs).
Sustainability 15 12698 g004
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Xiang, P.; Zhang, T.; Wu, Q.; Li, Q. Systematic Review of Degradation Processes for Microplastics: Progress and Prospects. Sustainability 2023, 15, 12698. https://doi.org/10.3390/su151712698

AMA Style

Xiang P, Zhang T, Wu Q, Li Q. Systematic Review of Degradation Processes for Microplastics: Progress and Prospects. Sustainability. 2023; 15(17):12698. https://doi.org/10.3390/su151712698

Chicago/Turabian Style

Xiang, Peng, Ting Zhang, Qian Wu, and Qiang Li. 2023. "Systematic Review of Degradation Processes for Microplastics: Progress and Prospects" Sustainability 15, no. 17: 12698. https://doi.org/10.3390/su151712698

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop