Synthesis of Nonclassical Heteroaryl C-Glycosides via Decarboxylative C-H Glycosylation.

A photoredox-promoted decarboxylative C-H glycosylation for the synthesis of nonclassical heteroaryl C-glycosides is reported. This methodology is characterized by an exceedingly simple reaction system, high diastereoselectivity, and good functional group tolerance. Moreover, the operational procedure is simple, and the gram-scale reaction highlights the practical applicability of this protocol.

Optimizing sludge dewatering with a combined conditioner of Fenton's reagent and cationic surfactant.

Enhancing sludge dewatering is of importance in reducing environmental burden and disposal costs. In this work, a cationic surfactant, cetyl trimethyl ammonium bromide (CTAB), was combined with Fenton's reagent for sludge dewatering. Results show that the Fenton-CTAB conditioning significantly promotes the sludge dewatering. Using combined techniques of response surface methodology and uniform design, dosages of Fe2+, H2O2, and CTAB for water content response were optimized to be 89, 276, and 233 mg/g dry solids (DS), respectively. The water content of sludge decreased from 79.0% to 66.8% under the optimal conditions. Compared with cationic polyacrylamide, the Fenton-CTAB system exhibited superior sludge dewatering performance. To gain insights into the mechanisms involved in sludge dewatering, the effects of Fenton-CTAB conditioning on the composition of extracellular polymeric substances (EPS) and the morphology of the sludge flocs were investigated. The decomposition of EPS into some dissolved organics and the release of proteins in tightly bound EPS facilitated the conversion of bound water to free water and further reduced the water content of sludge cake. After conditioning, morphology of sludge showed aggregation. Overall, the enhanced sludge dewatering by Fenton-CTAB treatment provides an efficient way for management of sewage sludge.

Iron-doped swine bone char as hydrogen peroxide activator for efficient removal of acetaminophen in water.

Bone char is a functional material obtained by calcining animal bones and is widely used for environmental remediation. In this work, iron was inserted into porcine bone-derived bone char via ion exchange to synthesize iron-doped bone char (Fe-BC) for efficient catalysis of hydrogen peroxide. This is the first time that Fe-BC has been used as a catalyst for the activation of H2O2. The effectiveness of the Fe-BC catalyst was influenced by the annealing temperature and the amount of iron doping. The results showed that the activation of H2O2 by the Fe-BC catalyst with the best catalytic performance could achieve 97.6% of APAP degradation within 30 min. Insights from electron paramagnetic resonance (EPR), free radical scavenging experiments and linear sweep voltammetry (LSV) proposed a reaction mechanism based on free radicals dominated degradation pathways (OH and O2-). Iron served as the primary active site in Fe-BC, with defect sites and oxygen-containing groups in the catalyst also contributing to the removal of pollutants. The Fe-BC/H2O2 system demonstrated resilience to interference from common anions (Cl-, NO3-, SO42- and HCO3-) in water, but was less effective against humic acid (HA). Based on the detection of intermediates produced during APAP degradation, possible degradation pathways of APAP were proposed and the toxicity of intermediates was evaluated. This work provides fresh insights into the use of heterogeneous Fenton catalysts for the removal of organic pollutants from water.

Probing the molecular interaction between photoaged polystyrene microplastics and fulvic acid.

As emerging contaminants, microplastics (MPs) are becoming a matter of global concern, and they have complex interactions with dissolved organic matter (DOM) widely present in aqueous environments. Here, we investigate the molecular interactions between aged polystyrene microplastics (PS-MPs) and fulvic acid (FA) under neutral conditions using a series of analytical techniques. The structural changes of FA and the binding interactions of PS-MPs with FA at a molecular level were explored by fluorescence and FT-IR combined with two-dimensional correlation spectroscopy (2D-COS). Results showed that photoaging of PS-MPs changed the sequence of structural variations with FA. Atomic force microscopy-infrared spectroscopy (AFM-IR) strongly demonstrated that the surface roughness of both pristine and aged PS-MPs greatly increased after FA addition. Meanwhile, AFM-IR and Raman spectroscopy revealed a stronger interaction between aged PS-MPs and FA. The content of oxygen-containing functional groups in PS-MPs increased after aging and after binding with FA, and surface distribution of these functional groups also changed. XPS analyses indicated that the oxygen content in PS-MPs increased after the interaction with FA and the increase in oxygen content was even greater in aged PS-MPs. Overall, these research findings are useful to understand the environmental impacts of DOM-MPs interactions and to address the uncertainty of MPs aging effect on their environmental behavior in aquatic ecosystems.

Influence mechanism of anions on iron doping into swine bone char: Promoting non-radical oxidation of acetaminophen in a Fenton-like system.

The application of iron-doped biochar in peroxymonosulfate (PMS) activation systems has gained increasing attention due to their effectiveness and environmental friendliness in addressing environmental issues. However, the behavioral mechanism of iron doping and the detailed 1O2 generation mechanism in PMS activation systems remain ambiguous. Here, we investigated the effects of three anions (Cl-, NO3-and SO42-) on the process of iron doping into bone char, leading to the synthesis of three iron-doped bone char (Fe-ClBC, Fe-NBC and Fe -SBC). These iron-doped bone char were used to catalyze PMS to degrade acetaminophen (APAP) and exhibited the following activity order: Fe-ClBC > Fe-NBC > Fe-SBC. Characterization results indicated that iron doping primarily occurred through the substitution of calcium in hydroxyapatite within BC. In the course of the impregnation, the binding of SO42- and Ca2+ hindered the exchange of iron ions, resulting in lower catalytic activity of Fe-SBC. The primary reactive oxygen species in the Fe-ClBC/PMS and Fe-NBC/PMS systems were both 1O2. 1O2 is produced through O2•- conversion and PMS self-dissociation, which involves the generation of metastable iron intermediates and electron transfer within iron species. The presence of oxygen vacancies and more carbon defects in the Fe-ClBC catalyst facilitates 1O2 generation, thereby enhancing APAP degradation within the Fe-ClBC/PMS system. This study is dedicated to in-depth exploration of the mechanisms underlying iron doping and defect materials in promoting 1O2 generation.

Visible-light-induced synthesis of heteroaryl C-glycosides via decarboxylative C-H glycosylation.

A photoredox promoted decarboxylative C-H glycosylation has been developed for the synthesis of heteroaryl C-glycosides. This methodology is characterized by its exceedingly simple reaction system, high diastereoselectivity and good functional group tolerance. Moreover, this innovative approach circumvents the need for high temperatures, transition metals, and photocatalysts, providing an environmentally friendly, straightforward, and efficient protocol.

Insight into iron oxychloride composite bone char for peroxymonosulfate activation: Mechanism of singlet oxygen evolution for selective degradation of organic pollutants.

The activity of iron-based catalysts in advanced oxidation processes (AOPs) is limited by the redox cycle of Fe(III) and Fe(II). In this work, iron oxychloride (FeOCl) with a unique layered structure was loaded on the bone char (BC) to enhance the activation of peroxymonosulfate (PMS). Characterization of the FeOCl-BC catalyst reveals that the loading of FeOCl changed the composition and structure of BC and BC reduced the bond gap of FeOCl. Acetaminophen (APAP) as a target pollutant could be almost completely degraded at neutral pH, and the removal rate reached 0.6597 min-1. APAP could also be selectively oxidized by FeOCl-BC/PMS system in the presence of some inorganic anions (SO42-, NO3-, and Cl-) and humic acid. Quenching experiments, electron paramagnetic resonance (EPR), chemical probes, and linear sweep voltammetry (LSV) confirm that the primary oxidation mechanism of the FeOCl-BC/PMS system was dominated by 1O2. The 1O2 was generated from the conversion of O2•- and the self-dissociation of PMS, involving the formation of metastable iron intermediates and the redox cycle of Fe(III) and Fe(II). The unique structure of FeOCl, the transport of lattice oxygen and the enrichment of electrons by carbon defects play an essential role in generating reactive species. In this work, the limitation of the redox cycle of Fe(III) and Fe(II) was broken by loading FeOCl on the surface of BC, and a new catalytic mechanism was proposed. This work provides a new perspective for the construction of efficient iron-based catalysts and the practical application of PMS-based AOPs.

Tungsten disulfide (WS2) is a highly active co-catalyst in Fe(III)/H2O2 Fenton-like reactions for efficient acetaminophen degradation.

The most important factor that restricts the decomposition of H2O2 in the Fe3+/H2O2 reaction is the slow cycling efficiency of reducing Fe3+ to Fe2+. In this study, the addition of tungsten disulfide (WS2) as a co-catalyst achieved a rapid cycling of the reaction rate-limiting step and a significant enhancement of H2O2 decomposition, which resulted in the effective degradation of acetaminophen (APAP). Results show that 99.6% of APAP (5 mg L-1) could be degraded by H2O2/Fe3+/WS2 system within 2.5 min. The conversion of Fe3+ to Fe2+ occurred mainly on the surface of WS2 due to the redox reaction of the exposed W4+ active sites with Fe3+ after the unsaturated S atoms were bound to protons. Electron paramagnetic resonance (EPR) and radical quenching experiments evaluated the contribution of hydroxyl radical (•OH) and superoxide radical (O2•-) in the degradation of pollutants. WS2 showed good recoverability after four cycles of the reaction. This study provides a new perspective to improve the efficiency of Fe3+/H2O2 and provides a reference for the involvement of transition metal sulfides in advanced oxidation processes (AOPs).

Interactions between microplastics and contaminants: A review focusing on the effect of aging process.

Microplastics (MPs) in the environment are a major global concern due to their persistent nature and wide distribution. The aging of MPs is influenced by several processes including photodegradation, thermal degradation, biodegradation and mechanical fragmentation, which affect their interaction with contaminants. This comprehensive review aims to summarize the aging process of MPs and the factors that impact their aging, and to discuss the effects of aging on the interaction of MPs with contaminants. A range of characterization methods that can effectively elucidate the mechanistic processes of these interactions are outlined. The rate and extent of MPs aging are influenced by their physicochemical properties and other environmental factors, which ultimately affect the adsorption and aggregation of aged MPs with environmental contaminants. Pollutants such as heavy metals, organic matter and microorganisms have a tendency to accumulate on MPs through adsorption and the interactions between them impact their environmental behavior. Aging enhances the specific surface area and oxygen-containing functional groups of MPs, thereby affecting the mechanism of interaction between MPs and contaminants. To obtain a more comprehensive understanding of how aging affects the interactions, this review also provides an overview of the mechanisms by which MPs interact with contaminants. In the future, there should be further in-depth studies of the potential hazards of aged MPs in different environments e.g., soil, sediment, aquatic environment, and effects of their interaction with environmental pollutants on human health and ecology.

Effects of photo-irradiation on mercury binding to dissolved organic matter: Insights from FT-IR and synchronous fluorescence two-dimensional correlation spectroscopy.

The binding interactions between Hg and dissolved organic matter (DOM) affect the fate and transport of Hg in the aquatic environment. Here, we investigate the effects of photo-irradiation on the binding characteristics of dissolved organic matter with Hg(II) using FT-IR and synchronous fluorescence two-dimensional correlation spectroscopy (2D-COS). Results showed that the binding of Hg(II) onto humic acid (HA) followed the order of humic-like fraction > fulvic-like fraction > protein-like fraction and photo-irradiation did not affect this order. The binding affinity of each site within the fluorescent fraction was affected by the photoreaction patterns. Pre-irradiation of HA before Hg(II) binding changed its structures and binding ability. UV irradiation showed a more obvious effect on Hg(II)-HA complexes than solar irradiation, and UV irradiation enhanced the reactivity of aromatic groups of HA. The amine or amide N-H of HA played a leading role in binding with Hg(II) in the dark, whereas the aromatic amine C-N became dominant after UV irradiation. In fulvic acid (FA), the aromatic hydrogen C-H played a leading role in Hg(II) binding in the dark, but solar irradiation promoted the binding ability of polysaccharide C-O and the carboxyl CO became dominant after UV irradiation. The response sensitivity of the fulvic-like fraction to Hg(II) was higher than that of the protein-like fraction in FA. Multiple types of sites binding to Hg(II) were verified in the fulvic-like fraction and protein-like fraction of FA. These findings provide new insight into photo-induced structural changes of DOM upon Hg binding.

Binding of methylmercury to humic acids (HA): Influence of solar radiation and sulfide addition reaction of HA.

Methylmercury (MeHg) is a neurotoxin that bioaccumulates in organisms and it forms strong complexes with reduced sulfur-containing ligands in dissolved organic matter (DOM). In the present study, the influences of solar radiation and sulfide addition reaction of humic acids (HA) on MeHg binding to HA were investigated using synchronous fluorescence and FT-IR two-dimensional correlation spectroscopic (2DCOS) analysis. Results showed that the complexation of fluorescent fractions of HA and sulfur-reacted HA (S-HA) with MeHg was not significantly affected by photoreaction treatments and the affinity of fluorescent fractions followed the order of protein-like fractions > humic-like fractions > fulvic-like fractions for both HA and S-HA. FT-IR 2DCOS analysis showed that the affinity of various binding sites in DOM for MeHg changed under different photoreaction treatments. Under dark treatment, small molecular compounds with low humification degree such as aromatic amino acids may be the site with the strongest binding ability to MeHg in HA, whereas aliphatic amino acids and sulfur-containing groups from sulfide addition reactions play a role in complexing of S-HA and MeHg. Under BS treatment (irradiation of DOM before MeHg binding), aliphatic compounds in HA preferentially bind to MeHg and aliphatic amino acids are the components with the strongest complexing ability; but for S-HA binding to MeHg, unsaturated functional groups and aromatic groups are more sensitive (alkenes > alkanes, phenols > alcohols). Under AS treatment (irradiation of DOM after MeHg binding), unsaturated bonds and aromatic compounds in HA preferentially bind to MeHg and aromatic amino acids show the strongest complexing ability; but for S-HA binding to MeHg, aliphatic groups show the strongest complexing ability (alkanes, alkenes > aromatics). These findings help us to better understand the complexation mechanisms between MeHg and DOM.

FT-IR and synchronous fluorescence two-dimensional correlation spectroscopic analysis on the binding properties of mercury onto humic acids as influenced by pH modification and sulfide addition.

Mercuric Hg2+ ion forms strong complexes with dissolved organic matter (DOM) in natural waters. The complexation of Hg2+ by sulfhydryl groups of DOM was regarded as the main mechanism for Hg2+-DOM interactions, particularly in anoxic sulfur and DOM-rich environments. In the present study, the influences of pH and sulfide addition on the molecular structure of Hg2+-DOM complexes and the characteristics of Hg2+ binding to DOM were investigated using FT-IR and synchronous fluorescence two-dimensional correlation spectroscopic analysis. Results showed that, during the Hg2+ binding process, the aromatic hydrogen CH in humic acids (HA) gave the fastest responses to pH perturbation and the S-reacted HA (S-HA) exhibited different reaction patterns from the unreacted HA. In S-HA, the esters/alcohols CO and carboxyl CO gave the fastest responses to Hg2+ binding. In the process of S-HA binding to Hg2+, the protein-like fractions including proteins, amino acids or monoaromatics played the leading role. Sulfide addition of HA enhanced the reactivity of small molecular weight compounds with low aromaticity and improved the binding ability of protein-like fractions to Hg2+. These findings provide a better understanding of the interaction mechanisms between Hg2+ and DOM at a molecular level and have important environmental implications in Hg2+ biogeochemical transformation, transport and cycling.

Environmental behaviors of microplastics in aquatic systems: A systematic review on degradation, adsorption, toxicity and biofilm under aging conditions.

Microplastics (MPs, < 5 mm) in the environment have attracted worldwide attention due to their wide distribution and difficulty in handling. Aging processes such as UV irradiation, biodegradation, physical abrasion and chemical oxidation can affect the environmental behavior of MPs. This review article summarizes different aging processes of MPs and subsequent effects on the adsorption of pollutants, the leaching of additives, and the toxicity of MPs. In addition, the formation process of biofilm on the surface of MPs and the interactions between biofilm and aged MPs are revealed. MPs can accumulate different environmental pollutants (organic pollutants, heavy metals, microorganisms, etc.) through surface adsorption, pore filling and distribution. Moreover, the aging of MPs affects their adsorption performance toward these pollutants due to a series of changes in their specific surface area and oxygen-containing functional groups. The release of some toxic additives such as phthalates after aging can enhance the toxic effects of MPs. Aging also changes the shape and size of MPs, which can affect the eating habits of the organisms and further increase the potential toxicity of MPs. This article conducts a systematical analysis and summary of the environmental behavior and physicochemical properties of MPs as well as the changes due to MPs aging, which helps to better understand the impact of aging on MPs in the environment. Future research on MPs aging should reduce the knowledge gap between laboratory simulation and actual conditions and increase the environmental relevance.

Interactions between polypropylene microplastics (PP-MPs) and humic acid influenced by aging of MPs.

As an emerging pollutant, microplastics (MPs) may interact with dissolved organic matter (DOM) which is prevalent in the aqueous environment. Meanwhile, the aging of MPs in the actual environment increases the uncertainty of their environmental fate. Here, the interaction mechanisms between pristine and aged polypropylene microplastics (PP-MPs) and humic acid (HA) at pH 7.0 were explored. Microstructural changes of HA were examined by fluorescence and Fourier transformation infrared (FT-IR) spectroscopy. Atomic force microscopy coupled with infrared (AFM-IR) and micro-Raman techniques were used to characterize and analyze the interacted PP-MPs. The addition of HA increased the surface roughness of both pristine and aged PP-MPs. Results of AFM-IR and Raman spectra showed that the interaction of PP-MPs with HA accelerated their surface oxidation and enhanced the characteristic signals. XPS spectra showed that the oxygen content ratio of pristine and aged PP-MPs increased by 0.95% and 1.48% after the addition of HA, respectively. PP-MPs after aging interacted more strongly with HA and there was a higher affinity between them. Two-dimensional correlation spectroscopy (2D-COS) combined with FT-IR spectra further elucidated the interaction mechanism at the molecular level. This work will help to evaluate the environmental impact of MPs in ecosystems and understand their interactions with DOM.

Effects of aging on environmental behavior of plastic additives: Migration, leaching, and ecotoxicity.

Microplastics (MPs), an emerging pollutant, are of global concern due to their wide distribution and large quantities. In addition to MPs themselves, various additives within MPs (such as plasticizers, flame retardants, antioxidants and heavy metals) may also have harmful effects on the environment. Most of these additives are physically bound to plastics and can therefore be leached from the plastic and released into the environment. Aging of MPs in the actual environment can affect the migration and release of additives, further increasing the ecotoxicological risk of additives to organisms. This work reviews the functions of several commonly used additives in MPs, and summarizes the representative characterization methods. Furthermore, the migration and leaching of additives in the human environment and marine environment are outlined. As aging promotes the internal chain breaking of MPs and the increase of specific surface area, it in turn stimulates the release of additives. The hazards of additive exposure have been elucidated, and various studies from the laboratory have shown that more toxic additives such as phthalates and brominated flame retardants can disrupt a variety of biological processes in organisms, including metabolism, skeletal development and so on. Increase of MPs ecological risk caused by the leaching of toxic additives is discussed, especially under the effect of aging. This study presents a systematic summary of various functional and environmental behaviors of additives in plastics, using weathering forces as the main factor, which helps to better assess the environmental impact and potential risks of MPs.

Activation of peroxymonosulfate by iron oxychloride with hydroxylamine for ciprofloxacin degradation and bacterial disinfection.

Iron oxychloride (FeOCl) is a known effective iron-based catalyst and has been used in advanced oxidation processes (AOPs). This study intends to achieve more facile free radicals generation from peroxymonosulfate (PMS) activation by exploring the Fe(III)/Fe(II) cycle of FeOCl in the presence of hydroxylamine (HA). With 0.2 g/L FeOCl, 1.5 mM PMS, and 1 mM HA, the PMS/FeOCl/HA system could effectively achieve 98.88% of the oxidative degradation of 5 mg/L ciprofloxacin (CIP) in 15 min and quickly inactivate 99.99% of E. coli (108 CFU/mL) in 5 min at near-neutral pH. HA played an important role in promoting the Fe(III)/Fe(II) cycle, thereby greatly improving the oxidation activity of the system. The reactive oxygen species (ROS) such as HO, SO4- and O2- were identified as the dominated free radicals produced in the system. The intermediate products of CIP detected by liquid chromatograph-mass spectrometer (LC-MS) and three possible degradation pathways of CIP were proposed. The presence of common anions in the PMS/FeOCl/HA system, including HCO3-, Cl-, SO42-, and NO3-, enhanced the degradation efficiency of CIP to varying degrees at the concentrations of 10 mM. Moreover, FeOCl maintained a high degradation capability for CIP after several recycles. This work offers a new promising means of catalyzing the PMS-based AOPs in the degradation of refractory organics.

Enhanced dewatering of activated sludge by acid assisted Heat-CaO2 treatment: Simultaneously removing heavy metals and mitigating antibiotic resistance genes.

High water content and accumulation of heavy metals and antibiotic resistance genes (ARGs) in sewage sludge limit its application. Fenton process has been widely used in sludge dewatering, but the use of hydrogen peroxide (H2O2) and generation of acid sludge are the main drawbacks. Here, a novel method of heat-CaO2 treatment was proposed to enhance sludge dewatering. Results showed that CaO2 (12.5 mg/g dry solids (DS)) combined with heat at 60 °C significantly improved the sludge dewaterability, e.g. the water content decreased from 79.9% to 69.2% and the specific resistance to filtration (SRF) decreased from 9.21 × 1013 to 1.51 × 1013 m/kg. At 62.5 mg CaO2/g DS, the final pH of filtrate was close to neutral and the good dewatering performance was still achieved. The improvement of sludge dewaterability was closely correlated with the decomposition of tightly-bound extracellular polymeric substances (EPS), lysis of the sludge cells, and increased particle size of the flocs. The distribution of bacterial community in the sludge has changed, leading to the decreases in the percentage of some ARGs. The concentrations of typical heavy metals wrapped in the sludge colloid network dramatically reduced. Economic analyses showed that the heat-CaO2 treatment was a promising method for sludge disposal.

Recent advances in municipal landfill leachate: A review focusing on its characteristics, treatment, and toxicity assessment.

Nowadays, sanitary landfilling is the most common approach to eliminate municipal solid waste, but a major drawback is the generation of heavily polluted leachates. These leachates must be appropriately treated before being discharged into the environment. Generally, the leachate characteristics such as COD, BOD/COD ratio, and landfill age are necessary determinants for selection of suitable treatment technologies. Rapid, sensitive and cost-effective bioassays are required to evaluate the toxicity of leachate before and after the treatment. This review summarizes extensive studies on leachate treatment methods and leachate toxicity assessment. It is found that individual biological or physical-chemical treatment is unable to meet strict effluent guidelines, whereas a combination of biological and physical-chemical treatments can achieve satisfactory removal efficiencies of both COD and ammonia nitrogen. In order to assess the toxic effects of leachate on different trophic organisms, we need to develop an appropriate matrix of bioassays based on their sensitivity to various toxicants and a multispecies approach using organisms representing different trophic levels. In this regard, a reduction in toxicity of the treated leachate will contribute to assessing the effectiveness of a specific remediation strategy.

Effects of accelerated aging on characteristics, leaching, and toxicity of commercial lead chromate pigmented microplastics.

It is of environmental significance to study the leaching performance of additives from microplastics (MPs) and further evaluate the toxicity of leachate to microalgae. Here, we investigated the effects of accelerated aging on characteristics, leaching, and toxicity of commercial lead chromate pigmented MPs. Results show that aging of MPs caused surface cracks and fragmentation, increased their surface area and carbonyl contents, and promoted the release of lead chromate pigment. Chromium (Cr) and lead (Pb) tend to leach under acidic condition, rather than neutral and alkali environment. Aging treatment facilitates the leaching performance and a high concentration of NaCl solution also favors the leaching process. Toxicology experiments demonstrate that only high concentration of leachate (>10 µg L-1) exerted significant inhibitory influence (p < 0.005) on cell photosynthesis of Microcystis aeruginosa. The growth inhibition of algal cells remarkably increased with increasing leachate concentrations. We observed more inhibiting effects on cell growth and photosynthesis using the leachates of aged MPs. Longer aging time leads to more release of Cr and Pb, rendering higher toxicity to microalgae. These novel findings will benefit us from assessing the leaching behavior of additives in MPs and their toxicological risks to aquatic organisms.

Aging of microplastics affects their surface properties, thermal decomposition, additives leaching and interactions in simulated fluids.

Most microplastics (MPs) have undergone extensive aging in the environment. Aged MPs exhibit different physical and chemical properties from unaged ones. Here, we studied the effects of accelerated aging on the characteristics and pyrolysis of commercial pigmented MPs, as well as pigments leaching and their interactions in simulated gastric and intestinal fluids of mammals. We report that the carbonyl index, surface area, and color change of MPs increased after aging treatment. Cracks and fragmentation of MPs facilitated the accessibility of light and oxygen to internal layer and therefore accelerated the aging process. TGA/GC-MS analysis showed that the high temperature resistance of MPs decreased after aging. Thermal decomposition of pigments and polyethylene occurred in temperature ranges of 340-406 °C and 406-550 °C, respectively. Mono (di)-alkenes and saturated alkanes were the thermal decomposition products of polyethylene. Aging of MPs also caused an increased release of pigments and prolonged aging time led to more release in simulated fluids. Pigments would result in fluorescence quenching of the enzymes through binding interactions once they were released from MPs into simulated fluids. Charge neutralization and polymer bridging accounted for the formation of pigment-enzyme complexes and flocs. These novel findings will allow us to better assess how aging process affects the characteristics, leaching, and toxicity of MPs.