Tunable schiff-based networks with different bonding sites for enhanced photocatalytic activity under visible-light irradiation: The effects of steric hindrance.

Organic polymers hold great potential in photocatalysis considering their low cost, structural tailorability, and well-controlled degree of conjugation for efficient electron transfer. Among the polymers, Schiff base networks (SNWs) with high nitrogen content have been noticed. Herein, a series of SNWs is synthesized based on the melamine units and dialdehydes with different bonding sites. The chemical and structural variation caused by steric hindrance as well as the related photoelectric properties of the SNW samples are investigated, along with the application exploration on photocatalytic degradation and energy production. The results demonstrate that only SNW-o based on o-phthalaldehyde responds to visible light, which extends to over 550 nm. SNW-o shows the highest tetracycline degradation rate of 0.02516 min-1, under 60-min visible light irradiation. Moreover, the H2O2 production of SNW-o is 2.14 times higher than that of g-C3N4. The enhanced photocatalytic activity could be ascribed to the enlarged visible light adsorption and intramolecular electron transfer. This study indicates the possibility to regulate the optical and electrical properties of organic photocatalysts on a molecular level, providing an effective strategy for rational supramolecular engineering to the applications of organic materials in photocatalysis.

Tween 80 surfactant-enhanced bioremediation: toward a solution to the soil contamination by hydrophobic organic compounds.

The occurrence of hydrophobic organic compounds (HOCs) in the soil has become a highly significant environmental issue. This problem has been exacerbated by the strong sorption of HOCs to the soils, which makes them unavailable for most remediation processes. More and more works show that surfactant-enhanced biological technologies offer a great potential to clear up HOCs-contaminated soils. This article is a critical review of HOCs removal from soils using Tween 80 (one of the mostly used nonionic surfactants) aided biological remediation technologies. The review begins with a discussion of the fundamentals of Tween 80-enhanced desorption of HOCs from contaminated soils, with special emphasis on the biotoxicity of Tween 80. Successful results obtained by Tween 80-enhanced microbial degradation and phytoremediation are documented and discussed in section 3 and section 4, respectively. Results show Tween 80-enhanced biotechnologies are promising for treating HOCs-contaminated soils. However, considering the fact that most of these scientific studies have only been conducted at the laboratory-scale, many improvements are required before these technologies can be scaled up to the full-scale level. Moreover, further research on mechanisms related to the interaction of Tween 80 with degrading microorganisms and the plants is in high demand.

Manganese-enhanced degradation of lignocellulosic waste by Phanerochaete chrysosporium: evidence of enzyme activity and gene transcription.

Lignolytic fungi initiate lignocellulose decay by producing extracellular oxidative enzymes. For better understanding the enzymatic degradation of lignocellulose by white-rot fungi, we investigated the effect of manganese on the organic matter loss, manganese peroxidase (MnP) activity, and manganese peroxidase gene (mnp) transcription levels during solid-state fermentation of rice straw with Phanerochaete chrysosporium. The results showed that the addition of manganese improved MnP activity and made it reach the peak earlier, promoted fungal growth at the early period (0-9 days), and enhanced the degradation of lignocellulosic waste. The total organic matter loss had a good correlation with fungal biomass during 30 days of cultivation, and manganese amendment promoted the ability of P. chrysosporium to degrade lignocellulose. Quantitative real-time RT-PCR revealed the differential expression of mnp1, mnp2, and mnp3: manganese amendment increased the transcription of mnp1 and mnp2 but not mnp3. The results indicated that manganese stimulated mnp transcription levels and played a post-transcriptional role in MnP production. These findings provide opportunity of development in enzymatic degradation of lignocellulosic waste by P. chrysosporium amended with manganese.

Microbial lipid production by oleaginous Rhodococci cultured in lignocellulosic autohydrolysates.

Metabolic synthesis of single cell oils (SCOs) for biodiesel application by heterotrophic oleaginous microorganisms is being hampered by the high cost of culture media. This study investigated the possibility of using loblolly pine and sweetgum autohydrolysates as economic feedstocks for microbial lipid production by oleaginous Rhodococcus opacus (R. opacus) PD630 and DSM 1069. Results revealed that when the substrates were detoxified by the removal of inhibitors (such as HMF-hydroxymethyl-furfural), the two strains exhibited viable growth patterns after a short adaptation/lag phase. R. opacus PD630 accumulated as much as 28.6 % of its cell dry weight (CDW) in lipids while growing on detoxified sweetgum autohydrolysate (DSAH) that translates to 0.25 g/l lipid yield. The accumulation of SCOs reached the level of oleagenicity in DSM 1069 cells (28.3 % of CDW) as well, while being cultured on detoxified pine autohydrolysate (DPAH), with the maximum lipid yield of 0.31 g/l. The composition of the obtained microbial oils varied depending on the substrates provided. These results indicate that lignocellulosic autohydrolysates can be used as low-cost fermentation substrates for microbial lipid production by wild-type R. opacus species. Consequently, the variety of applications for aqueous liquors from lignocellulosic pretreatment has been expanded, allowing for the further optimization of the integrated biorefinery.

Experimental investigation on NOx emission characteristics of a new solid fuel made from sewage sludge mixed with coal in combustion.

In this article, a new briquette fuel (SC), which was produced by the mixture of coal fines (25.9%), sewage sludge (60.6%), lignin (4.5%), tannic acid (4.5%) and elemental silicon (4.5%), was provided. Then, in a high temperature electric resistance tubular furnace, the total emissions of NO2 and NO, effects of combustion temperature, air flow rate and heating rate on NOx (NO, NO2) emissions of SC were studied during the combustion of SC; furthermore, effects of additives on hardness were also analysed, and the X-ray photoelectron spectroscopy was applied to investigate the reduced NOx emission mechanism. The research results showed that, compared with the characteristics of briquette fuel (SC0) produced only by the mixture of coal and sewage sludge (the ratio of coal to sewage sludge was the same as that of SC), the Meyer hardness of SC was 12.6% higher than that of SC0 and the emissions of NOx were 27.83% less than that of SC0 under the same combustion conditions. The NOx emissions of SC decreased with the adding of heating rate and increased with the rise of air flow rate. When the temperature was below 1000 °C, the emissions of NOx increased with the elevated temperature, however, further temperature extension will result in a decreasing in emissions of NOx. Furthermore, the X-ray photoelectron spectroscopy results proposed that the possible mechanism for the reduction of NOx emissions was nitrogen and silicon in SC to form the compounds of silicon and nitrogen at high temperatures.

Diversity of two-domain laccase-like multicopper oxidase genes in Streptomyces spp.: identification of genes potentially involved in extracellular activities and lignocellulose degradation during composting of agricultural waste.

Traditional three-domain fungal and bacterial laccases have been extensively studied for their significance in various biotechnological applications. Growing molecular evidence points to a wide occurrence of more recently recognized two-domain laccase-like multicopper oxidase (LMCO) genes in Streptomyces spp. However, the current knowledge about their ecological role and distribution in natural or artificial ecosystems is insufficient. The aim of this study was to investigate the diversity and composition of Streptomyces two-domain LMCO genes in agricultural waste composting, which will contribute to the understanding of the ecological function of Streptomyces two-domain LMCOs with potential extracellular activity and ligninolytic capacity. A new specific PCR primer pair was designed to target the two conserved copper binding regions of Streptomyces two-domain LMCO genes. The obtained sequences mainly clustered with Streptomyces coelicolor, Streptomyces violaceusniger, and Streptomyces griseus. Gene libraries retrieved from six composting samples revealed high diversity and a rapid succession of Streptomyces two-domain LMCO genes during composting. The obtained sequence types cluster in 8 distinct clades, most of which are homologous with Streptomyces two-domain LMCO genes, but the sequences of clades III and VIII do not match with any reference sequence of known streptomycetes. Both lignocellulose degradation rates and phenol oxidase activity at pH 8.0 in the composting process were found to be positively associated with the abundance of Streptomyces two-domain LMCO genes. These observations provide important clues that Streptomyces two-domain LMCOs are potentially involved in bacterial extracellular phenol oxidase activities and lignocellulose breakdown during agricultural waste composting.

Enhanced removal of ethylbenzene from gas streams in biotrickling filters by Tween-20 and Zn(II).

The effects of Tween-20 and Zn(II) on ethylbenzene removal were evaluated using two biotrickling filters (BTFs), BTF1 and BTF2. Only BTF1 was fed with Tween-20 and Zn(II). Results show that ethylbenzene removal decreased from 94% to 69% for BTF1 and from 74% to 54% for BTF2 with increased organic loading from 64.8 to 189.0 g ethylbenzene/(m³·hr) at EBRT of 40 sec. The effect of EBRT (60-15 sec) at a constant ethylbenzene inlet concentration was more significant than that of EBRT (30-10 sec) at a constant organic loading. Biomass accumulation rate within packing media was reduced significantly.

A tyrosinase biosensor based on ordered mesoporous carbon-Au/L-lysine/Au nanoparticles for simultaneous determination of hydroquinone and catechol.

A novel biosensor was developed based on tyrosinase immobilization with ordered mesoporous carbon-Au (OMC-Au), L-lysine membrane and Au nanoparticles on a glassy carbon electrode (GCE). It was applied for the simultaneous determination of dihydroxybenzene isomers using differential pulse voltammetry (DPV). The tyrosinase/OMC-Au/L-lysine/Au film was characterized by scanning electron microscopy (SEM) and impedance spectra. Under optimized conditions, the DPV study results for two isomers, hydroquinone (HQ, 1,4-dihydroxybenzene) and catechol (CC, 1,2-dihydroxybenzene) showed low peak potentials, and the peak-to-peak difference was about 135.85 mV, which ensured the anti-interference ability of the biosensor and made simultaneous detection of dihydroxybenzene isomers possible in real samples. DPV peak currents increased linearly with concentration over the range of 4.0 × 10(-7) to 8.0 × 10(-5) M, and the detection limits of hydroquinone and catechol were 5 × 10(-8) M and 2.5 × 10(-8) M (S/N = 3), respectively. The tyrosinase biosensor exhibited good repeatability and stability. In addition, the response mechanism of enzyme catalysed redox on the OMC-Au/L-lysine/Au film modified electrode based on electrochemical study was discussed. The proposed method could be extended for the development of other enzyme-based biosensors.

Microplastics influence the fate of antibiotics in freshwater environments: Biofilm formation and its effect on adsorption behavior.

Microplastics (MPs) are substrates available for biofilms colonization in natural water environments. The biofilms formation may enhance the ability of MPs to adsorb harmful contaminants. Herein, we investigated the biofilms formation of three different MPs (PVC, PA and HDPE) in simulated natural environment, and observed the chemical structure, charge property, hydrophobicity and other properties of MPs affect microbial biomass and community composition. More importantly, potential pathogens were found in all three MPs biofilms. Furthermore, the adsorption capacities of original MPs and biological aging MPs for norfloxacin (NOR) was compared. HDPE has the largest adsorption capacity for NOR, while PA has the smallest adsorption capacity for NOR. It was concluded that the formation of biofilms enhanced the adsorption of NOR by 50.60 %, 24.17 % and 46.02 % for PVC, PA and HDPE, respectively. In addition, hydrogen-bond interaction, electrostatic interaction and hydrophobic interaction were found to dominate the adsorption of NOR by MPs. Our study contributed to improve the understanding of the interactions between aging MPs and contaminants in the natural water environments, and provided essential information for ecological risk assessment of MPs.

Selective catalytic reduction (SCR) of NO by urea loaded on activated carbon fibre (ACF) and CeO2/ACF at 30 degrees C: the SCR mechanism.

Selective catalytic reduction (SCR) of NO by urea loaded on rayon-based activated carbon fibre (ACF) and CeO2/ACF (CA) was studied at ambient temperature (30 degrees C) to establish a basic scheme for its reduction. Nitric oxide was found to be reduced to N2 with urea deposited on the ACF and CA. When oxygen was present, the greater the amount of loaded urea (20-60%), the greater the NO(x) conversions, which were between 72.03% and 77.30%, whereas the NO(x) conversions were about 50% when oxygen was absent. Moreover, when the urea was loaded on CA, a catalyst containing 40% urea/ACF loaded with 10% CeO2 (UCA4) could yield a NO(x) conversion of about 80% for 24.5 h. Based on the experimental results, the catalytic mechanisms of SCR with and without oxygen are discussed. The enhancing effect of oxygen resulted from the oxidation of NO to NO2, and urea was the main reducing agent in the SCR of loaded catalysts. ACF-C was the catalytic centre in the SCR of NO of ACF, while CeO2 of urea-loaded CA was the catalytic centre.

Microplastics in landfill and leachate: Occurrence, environmental behavior and removal strategies.

Plastic wastes buried in landfill are gradually broken and decomposed into microplastics under physical, chemical and biological effects, bringing environmental risks to the exploitation of waste resources. Landfill leachate as a potential source of environmental microplastics has not good attention. Microplastics in leachate carry toxic and harmful pollutants and antibiotic resistance genes, and these vectors pose greater risks to human and environmental health without systematic treatment. Recently, the main technologies of landfill leachate treatment process include order batch activated sludge process, membrane biological reaction process, flocculation process, combined filtration process, and constructed wetland process. However, there is still little knowledge about microplastic removal of the existing leachate treatment facilities, and some technologies to alleviate the sources of such microplastics should be timely developed. This paper systematically summarizes the occurrence of plastics, microplastics and nanoplastics in leachate and their interactive pollution with other toxic pollutants. Meanwhile, the prospects of their environmental behaviors in landfill and leachate are put forward. The microplastic removal by existing leachate treatment equipment and the limitations and challenges to upgrading process of development and implementation are also discussed. The paper can provide a scientific basis for studying the fate of microplastics in landfill and leachate.

Advanced oxidation processes for the elimination of microplastics from aqueous systems: Assessment of efficiency, perspectives and limitations.

Microplastics act as a vector of heavy metals, organic pollutants, pathogens and resistance genes in the environment further aggravate the pollution of plastics. The conventional wastewater/water treatment processes can physically capture and remove most of microplastics, but the success rates varies. How to quickly remove a large amount of microplastics from aqueous system is a key research topic at present. Recently, advanced oxidation processes (AOPs) as a green elimination strategy has attracted attention because of its effective elimination, strong destruction and safety. The molecular chain of microplastics can be gradually degraded into small molecular organics until H2O and CO2 by strong oxidizing free radical produced by AOPs. Unfortunately, problematically, the elimination of microplastics in aqueous system by AOPs is recently carried out on a laboratory scale. The application and implementation of this strategy are restricted by long reaction time, low liquid phase degradation efficiency and the formation of nanoplastics. Generally, the technology is still in its infancy, and most studies are carried out under laboratory conditions. The degradation of microplastics in aqueous system also needs appropriate conditions, but it is not always feasible under field conditions in AOPs. Although AOPs can be used as a green degradation technology to eliminate microplastics in aqueous systems in theory, it still needs to be furtherly explored in practical application. Consequently, before AOPs as a green elimination strategy is successfully applied to the effective remove microplastics, more in-depth research is still required, such as the setting from single condition to complex environment, the transfer from laboratory scale to field scale, and systematic toxicity evaluation of corresponding products.

Recent advances in impacts of microplastics on nitrogen cycling in the environment: A review.

Nitrogen cycling plays a decisive role in biogeochemistry, and largely depends on microbial driven nitrogen transformation. The environmental problems caused by microplastics are becoming more serious, and the analysis and control of its pollution in the environment have become a research hotspot in the field. The nitrogen transformation and nitrogen cycling in the environment are mainly driven by microorganisms in the environment, and the existence of microplastics can affect the microbial population, abundance and type, thus affecting the transformation of nitrogen. The effect of microplastics on microorganisms involved in nitrogen transformation is briefly described. This paper mainly reviews the research progress on the impacts of microplastics on nitrogen transformation and nitrogen cycling in water, soil, sediment and sewage sludge. Microplastic type, size and concentration can cause obvious difference in the impacts of microplastics on nitrogen transformation. Then, response and mechanism of microplastics to microorganism mediated nitrogen transformation and nitrogen cycling are introduced. Processes of nitrogen transformation are affected by interfering with microorganism diversity and structure, enzyme activities and related coding genes and oxygen flux. Additionally, additives released from microplastics can also affect the microbial activity. However, mechanisms of microplastics on environmental nitrogen transformation and nitrogen cycling are not fully understood due to the lack of relevant research. There are effective strategies to evaluate complex environmental systems, prolong action time, strengthen multi factor and multi-level research, and assist molecular biology and stable isotope technology. This review article can provide valuable insights into the impact of microplastics on microorganisms mediated nitrogen transformation processes and evaluate the impact on ecological and environmental health.

The role of microplastics in altering arsenic fractionation and microbial community structures in arsenic-contaminated riverine sediments.

The ability of microplastics (MPs) to interact with environmental pollutants is of great concern. Riverine sediments, as sinks for multi-pollutants, have been rarely studied for MPs risk evaluation. Meanwhile, MPs generated from biodegradable plastics are questioning the safety of the promising materials. In this study, we investigated the effects of typical non-degradable polyethylene (PE) and biodegradable polylactic acid (PLA) MPs on sediment enzymes, arsenic (As) fractionation, and microbial community structures in As-contaminated riverine sediments. The results indicated that the presence of MPs (1% and 3%, w/w) led As transformed into more labile and bioavailable fractions in riverine sediments, especially under higher As and MPs levels. Analysis on microbial activities and community structures confirmed the strong potential of MPs in inhibiting microbial activities and shifting bacterial community succession patterns through enrichment of certain microbiota. Moreover, biodegradable PLA MPs presented stronger alterations in arsenic fractionation and microbial community structures than PE MPs did, which might be jointly attributed to adsorption behaviors, microbial alterations, and potential PLA degradation behaviors. The study indicated that MPs contamination increased As mobility and bioavailability, and shifted microbial communities in riverine sediments. Moreover, biodegradable MPs might lead to stronger microbial alterations and increases in As bioavailability, acting as a threat to ecological safety, which needed further exploration.

Biofilm on microplastics in aqueous environment: Physicochemical properties and environmental implications.

The excellent properties of plastics make them widely used all over the world. However, when plastics enter the environmental medium, microplastics will inevitably be produced due to physical, chemical and biological factors. Studies have shown that microplastics have been detected in terrestrial, aquatic and atmospheric environments. In addition, the presence of microplastics will provide a new artificial adhesion substrate for biofilms. It has been proved that the formation of biofilms could significantly change some properties of microplastics. Some studies have found that microplastics attached with biofilms have higher environmental risks and eco-toxicity. Therefore, considering the widespread existence of microplastics and the ecological risks of microplastic biofilms, the physical and chemical properties of biofilms on microplastics and their impact on microplastics in aqueous environment are worth reviewing. In this paper, we comprehensively reviewed representative studies in this area. Firstly, this study reviews that the existence of biofilms could change the transport and deposition of microplastics. Subsequently, the presence of biofilms would enhance the ability of microplastics to accumulate pollutant, such as persistent organic pollutants, heavy metals and antibiotics. Moreover, the effect of biofilms on microplastics enrichment of harmful microorganisms is summarized. Finally, some future research needs and strategies are proposed to better understand the problem of biofilms on microplastics.

Lignocellulosic biomass derived N-doped and CoO-loaded carbocatalyst used as highly efficient peroxymonosulfate activator for ciprofloxacin degradation.

Burning lignocellulosic biomass wastes in an outdoor atmosphere has placed heavy burden on ecological environment and increased risk on human health. Converting solid agricultural wastes into functional materials is a research hotspot. In this study, N-doped and CoO-loaded carbocatalyst (CoO-N/BC) was successfully synthesized from the cotton stalk biomass via a simple synthesis process of impregnation and carbonization. Compared with cotton stalk biomass derived pristine biochar, the CoO-N/BC possessed a higher specific surface area (466.631 m2 g-1vs 286.684 m2 g-1) as well as a better catalytic performance in the activation of peroxymonosulfate (PMS) for CIP degradation. The superior catalytic efficiency was ascribed to the directional flow of electrons on the well-organized carbon network of CoO-N/BC, which accelerated electron migration and improved electron conduction ability. Based on the results of radical quenching experiment and electron paramagnetic resonance (EPR), both radical and non-radical process conjointly led to the stepwise decomposition of CIP, and singlet oxygen (1O2) mediated non-radical pathway was discovered to play a dominant role. Besides, the carbon-bridge mediated non-radical pathway was proved to accelerate this degradation process through the experiments of prolong the time of adding CIP at different time intervals. Nitrogen doped sites and CoO active sites as well as defects formed in sp2-hybridized carbon network were supposed to be the active sites for PMS. Furthermore, EIS and LSV were employed to confirm the electron transfer mediated non-radical process of reaction system. This work provides a modified strategy for the disposition of lignocellulosic biomass wastes and illuminates the underlying mechanism of heterogeneous catalysis by CoO-N/BC.

Performance of biotrickling filters packed with structured or cubic polyurethane sponges for VOC removal.

Two identical bench-scale biotrickling filters (BTFs), BTF 1 and BTF 2, were evaluated for toluene removal at various gas empty bed contact times (EBCTs) and organic loadings. BTF 1 and BTF 2 were packed with structured and cubic synthetic polyurethane sponges, respectively. At a constant toluene loading of 16 g/(m3.hr), toluene removal efficiencies decreased from 98.8% to 64.3% for BTF 1 and from 98.4% to 74.1% for BTF 2 as gas EBCT decreased from 30 to 5 sec. When the toluene loading increased from 35 to 140 g/(m3.hr) at a gas EBCT of 30 sec, the removal efficiencies decreased from 99.1% to 77.4% for BTF 1 and from 99.0% to 81.5% for BTF 2. The pressure drop for both BTFs increased with increased air flow rate, and did not significantly vary while the toluene loading was increased under similar operation conditions. BTF 1 and BTF 2 could start up successfully within 19 and 27 days, respectively, when packed with fresh sponge media, and the performances could be restored in 3-7 days after biomass was removed and wasted from the media. BTF 2 displayed higher removal efficiency even under shorter EBCT or higher loading rate than BTF1 when other operation conditions were similar, while it showed lower pressure drop than BTF 1 during the whole period of operation. These results demonstrated that both BTFs could treat waste gas containing toluene effectively.

Effects of virgin microplastics on the transport of Cd (II) in Xiangjiang River sediment.

River sediments are considered as sinks of microplastics (MPs). Although numerous studies have been conducted on MPs pollution in river sediments, the impact of MPs on the environmental behavior of Cd (II) in river sediments is still unknown. In this work, the effects of six MPs (polyethylene, polypropylene, polystyrene, polyvinyl chloride, polymethyl methacrylate and polylactic acid) on the adsorption of Cd (II) by Xiangjiang River sediment and the transport of Cd (II) in sediment were studied. The results showed that the adsorption ability of sediment to Cd (II) decreased with the increase of the content of MPs in sediment. When the content of MPs in sediment increased to 10%, polypropylene had the greatest effect on the adsorption affinity of sediments to Cd (II). Moreover, the addition of MPs accelerated transport of Cd (II) in sediment, and the transport of Cd (II) in sediment increased with the increase of the content of MPs. The reason may be that after adding MPs, the adsorption capacity of sediment to Cd (II) decreases, and the mass transfer resistance of Cd (II) to sediment reduces, which leads to faster transport of Cd (II) in sediment. Especially, when the content of MPs in sediment increased to 10% (w/w), the saturation point of the breakthrough curve decreased by about 70 pore volumes. This work hopes to provide helpful views on the environmental behavior and risk assessment of Cd (II) in the presence of MPs.

Smoked cigarette butts: Unignorable source for environmental microplastic fibers.

The pollution of microplastics and their potential environmental hazards have attracted considerable attention of the public. Cigarette butts, composed of cellulose acetate, are one of the most common plastic pollutants in the environment. Of all the litter that is discarded at will, cigarette butts are the most acceptable. Cigarette butts are dangerous pieces of plastic, but are usually not handled properly and consist of more than 15,000 detachable strands of plastic fiber. Discarded cigarette butts may be carried into rivers and lakes, and finally into the ocean. The plastic fibers will continuously release microplastic fibers into the environment. About 300,000 tons of potential microplastic fibers may enter the aquatic environment from this source per annum. Additionally, toxic substances, such as nicotine, carcinogenic tar, and polycyclic aromatic hydrocarbons, have strong toxic effect, which will cause serious damage to aquatic organisms. However, the mechanism and rate of microplastic fibers release from smoked cigarette butts and the joint toxicity of microplastic fibers and toxic pollutants to aquatic organisms are still in the initial stage. Therefore, it is necessary to understand the mechanism of cigarette butts releasing microplastic fibers, the potential impact on the environment and possible measures to reduce the impacts of cigarette butt litter. The aim of this paper is to evaluate the potential sources of smoked cigarette butts as environmental fiber microplastics and the potential ecological effects of the released microplastic fibers on the ecosystem. In addition, some ways which could help to tackle problem of smoked cigarette butts pollution have also been proposed.

Presence of microplastics in drinking water from freshwater sources: the investigation in Changsha, China.

We investigated the abundance of microplastics in freshwater, treated water, and household tap water from the drinking water supply chain in Changsha, China. The abundance was 2173-3998 (mean = 2753), 338-400 (mean = 351.9), and 267-404 (mean = 343.5) particles L-1 in freshwater, treated water, and tap water, respectively. Fibrous and fragments made up the majority (> 70%) in all water samples, and most polymers were composed of polyethylene, polypropylene, and polyethylene terephthalate. Microplastics in tap water were related to materials of transportation pipelines in drinking-water supply chain. Although plastics are corrosion-resistant, the slight fragmentation and abrasion may occur during drinking water treatment transportation. This study provided a proof for the occurrence of microplastics in drinking water, which may offer a reference for microplastic removal during drinking water treatment, and the formulation of standards for microplastic content in drinking water.