Competition among Refined Hollow Structures in Schiff Base Polymer Derived Carbon Microspheres.

Synthetic polymer-derived hollow carbon spheres have great utilitarian value in many fields for which the synthesis of proper polymer precursors is a key process. The exploration of new suitable polymer precursors and the construction of refined hollow structures in emerging polymers are both of great significance for synthetic methodology and novel carbon materials. Here, for the first time Schiff base polymer (SBP) colloid spheres with refined hollow structures were synthesized by tandem gradient growth and confined polymerization processes. The Hill equation was employed as a mathematical model to explain the gradient growth of SBP spheres. The size-dependent inner structure of SBP spheres can be adjusted from hollow to multichamber-surrounded hollow, and then to a multichamber structure. SBP-derived carbon spheres having similar surface area and chemical composition but different inner structures provide an effective way to investigate the relationship between inner structure and performance.

Outcome and predictive factors for perforation in orthodontic rubber band-assisted endoscopic submucosal dissection of fibrotic colorectal lesions.

Endoscopic submucosal dissection (ESD) of fibrotic colorectal lesions is difficult and has a high complication rate. There are only a few reports on the utility of orthodontic rubber band (ORB) traction in reducing the difficulty of this procedure. This study aimed to investigate the risk factors for perforation when applying ORB traction during ESD of fibrotic colorectal lesions. We continuously collected the clinical data of 119 patients with fibrotic colorectal lesions who underwent ESD with ORB and clip traction between January 2019 and January 2024. Possible risk factors for perforation were analyzed. The median ORB-ESD operative time was 40 (IQR 28-62) min, and the en bloc and R0 resection rates were 94.1% and 84.0%, respectively. Perforation occurred in 16 of 119 patients (13.4%). The lesion size, lesion at the right half of the colon or across an intestinal plica, the degree of fibrosis, operation time, and the surgeon's experience were associated with perforation during ORB-ESD (P < 0.05). Multivariate logistic regression analysis showed that lesions in the right colon (OR 9.027; 95% CI 1.807-45.098; P = 0.007) and those across an intestinal plica (OR 7.771; 95% CI 1.298-46.536; P = 0.025) were independent risk factors for perforation during ORB-ESD. ORB-ESD is an effective and feasible approach to treat fibrotic colorectal lesions. Adequate preoperative evaluation is required for lesions in the right colon and across intestinal plicas to mitigate the risk of perforation.

Formula optimization and in vivo study of poly(L-glutamic acid)-g-methoxy poly(ethylene glycol)/combretastatin A4/BLZ945 nanoparticles for cancer therapy.

Poly(L-glutamic acid)-g-methoxy poly(ethylene glycol)/Combretastatin A4 (CA4)/BLZ945 nanoparticles (CB-NPs) have shown great potential in synergistic cancer therapy. However, it is still unclear how the nanoparticles' formula, such as injection dose, active agent ratio, and drug loading content, affects the side effects and in vivo efficacy of CB-NPs. In this study, a series of CB-NPs with different BLZ945/CA4 (B/C) ratios and drug loading contents were synthesized and evaluated on a hepatoma (H22) tumor-bearing mice model. The injection dose and B/C ratio were found to have a significant influence on the in vivo anticancer efficacy. The CB-NPs 20 with B/C weight ratio of 0.45/1, and total drug loading content (B + C) of 20.7 wt%, showed the highest potential for clinical application. Systematic pharmacokinetics, biodistribution, and in vivo efficacy evaluation for CB-NPs 20 have been finished, which may provide significant instruction for medicine screening and clinical application.

Preparation of an Ultrahigh-DAR PDL1 monoclonal antibody-polymeric-SN38 conjugate for precise colon cancer therapy.

Antibody-drug conjugates (ADCs) are the most potent active tumor-targeting agents used clinically. However, the preparation of ADCs with high drug-to-antibody ratios (DARs) remains a major challenge. Herein, a Fab-nondestructive SN38-loaded antibody-polymeric-drug conjugate (APDC), aPDL1-NPLG-SN38, was prepared that had a DAR as high as 72 for the first time, by increased numbers of payload binding sites via the carboxyl groups of poly (l-glutamic acid) (PLG). The bonding of Fc-III-4C peptide with PLG-graft-mPEG/SN38 (Fc-NPLG-SN38) was achieved using a click reaction between azide and DBCO groups. The aPDL1-NPLG-SN38 conjugate was then synthesized by the high-affinity interaction between the Fc-III-4C peptide in Fc-NPLG-SN38 and the crystallizable fragment (Fc) of PDL1 monoclonal antibody (aPDL1). This approach avoided the potential deleterious effects on the Fab structure of the monoclonal antibody. The aqueous environment used in its preparation helped maintain monoclonal antibody recognition capability. Through the specific recognition by aPDL1 of PDL1 that is highly expressed on MC38 tumors, the accumulation of aPDL1-NPLG-SN38 in the tumors was 2.8-fold greater than achieved with IgG-NPLG-SN38 that had no active tumor-targeting capability. aPDL1-NPLG-SN38 exhibited excellent therapeutic properties in both medium-sized and large MC38 tumor animal models. The present study provides the details of a novel preparation strategy for SN38-loaded ADCs having a high DAR.

Polystyrene nanoplastics change the functional traits of biofilm communities in freshwater environment revealed by GeoChip 5.0.

There is an increasing concern regarding the potential effects of nanoplastics (NPs) on freshwater ecosystems. Considering the functional values of biofilms in freshwater, knowledge on whether and to what extent NPs can influence the ecosystem processes of biofilms were still limited. Herein, the freshwater biofilms cultured in lab were exposed to 100 nm polystyrene NPs (PS-NPs) of different dosages (1 and 10 mg/L) for 14 days. Confocal laser scanning microscope observation indicated that biofilms were dominated by filamentous, and spiral algae species and the intensity of extracellular polymeric substances increased under PS-NPs exposure. GeoChip 5.0 analysis revealed that PS-NPs exposure triggered a significant increase in functional genes α diversity (p < 0.05) and altered biofilms' functional structure. Furthermore, the abundance of genes involved in the total carbon and nitrogen cycling were increased under PS-NPs exposure. The abundance of nitrogen fixation genes experienced the most pronounced increase (24.4%) under 1 mg/L PS-NPs treatment, consistent with the increase of ammonium in overlying water. Whereas antibiotic resistance genes and those related to photosynthetic pigments production were suppressed. These results provided direct evidence for PS-NPs' effects on the biofilm functions in terms of biogeochemical cycling, improving our understanding of the potentials of NPs on freshwater ecosystems.

Effects of Biofilms on Trace Metal Adsorption on Plastics in Freshwater Systems.

The formation of plastisphere on plastics and their potential impact on freshwater ecosystems have drawn increasing attention. However, there is still limited information about the effects of plastisphere on the heavy metal adsorption capacity and the related mechanism of plastic debris in different freshwaters. Herein, the trace metal adsorption capacity, kinetics and adsorption mechanisms of virgin and biofilm-covered plastic debris were investigated. Polypropylene (PP) and polyethylene terephthalate (PET) plastic debris were placed in three freshwaters (Xuanwu Lake, Donghu Lake and the Qinhuai River) for 45 days to incubate biofilms. Batch adsorption experiments were performed to compare the adsorption processes of trace metal on virgin and biofilm-covered plastics. Results showed that biofilms increase the adsorption of metals on plastics, and the adsorption isotherms were well fitted by the Langmuir model. Furthermore, the adsorption capacities for lead (Pb(II)) were higher than that of cadmium (Cd(II)) and zinc (Zn(II)), with 256.21 and 277.38 µg/g (Pb(II)) adsorbed in biofilm-covered PP and PET, respectively, in Xuanwu Lake. The adsorption kinetics of metals on plastic debris were significantly affected by the biofilms, by switching the intraparticle diffusion for virgin plastic debris to film diffusion for the biofilm-covered plastic debris. Moreover, the complexation of functional groups within the biofilms might mainly contribute to the increases of metal adsorption, involving the participation of oxygen and nitrogen groups. Overall, these results suggested that biofilms reinforce the potential role of plastics as a carrier of trace metals in freshwaters.

[Aging Process and DOC Analysis of Four Different Types of Plastic Particles in Freshwater Systems].

Although the pollution of freshwater systems by microplastics and the resulting ecological effects have attracted widespread attention from scholars at home and abroad, the fragmentation of different types of microplastics in the natural environment has not yet received enough attention. To analyze the fragmentation processes and products of different types of microplastics, a 40 d natural light fragmentation experiment was carried out using four microplastics commonly found in water:polystyrene (PS), low-density polyethylene (LDPE), polypropylene (PP), and polyhydroxybutyrate (PHB). The pH, ORP, EC, and DO of the four types of plastic-aging liquids changed significantly during the aging process. During the weathering process, cracks and pores formed on the surface of LDPE and were later identified through scanning electron microscopy. Fourier transform infrared spectrometry indicated that the carbonyl index of LDPE increased the most in the experiment (an increase of 31.48%), suggesting that PP experienced significant aging. Dissolved organic carbon (DOC), a product of microplastics fragmentation, increased as weathering time progressed, and the concentration of DOC increased significantly after weathering for about 40 d. Compared with the baseline value, the concentration of DOC from PHB, PP, and LDPE in the leaching solution increased significantly, by 61.29%, 69.49%, and 89.15%, respectively. These results suggest that evident aging of microplastics in natural aquatic environments releases significant amounts of dissolved organic matter, and the ecological effects of this should be the subject of future research.

Biofilm influenced metal accumulation onto plastic debris in different freshwaters.

Microbial biofilms can rapidly colonize plastic debris in aquatic environments and subsequently, accumulate chemical pollutants from the surrounding water. Here, we studied the microbial colonization of different plastics, including polyethylene terephthalate (PET), polypropylene (PP), polyvinyl chloride (PVC), and polyethylene (PE) exposed in three freshwater systems (the Qinhuai River, the Niushoushan River, and Donghu Lake) for 44 days. We also assessed the biofilm mass and associated metals attached to plastics. The plastics debris characteristics, such as contact angle and surface roughness, greatly affected the increased biofilm biomass. All types of metal accumulation onto the plastic substrate abundances significantly higher than the concentrations of heavy metal in the water column, such as Ba (267.75 µg/g vs. 42.12 µg/L, Donhu Lake), Zn (254 µg/g vs. 0.023 µg/L the Qinhuai River), and Cr (93.75 µg/g vs. 0.039 µg/L, the Niushoushan River). Compared with other metals, the heavy metal Ba, Cr and Zn accumulated easily on the plastic debris (PET, PP, PVC, and PE) at all incubation sites. Aquatic environmental factors (total nitrogen, total phosphorus, and suspended solids concentrations) largely shaped metal accumulation onto plastic debris compared with plastic debris properties.

Effects of biofilm colonization on the sinking of microplastics in three freshwater environments.

Microplastics (MPs) have frequently been detected in freshwater environments, and there is growing concern about their ecological effects, especially the influence of the "plastisphere" on the freshwater ecosystems. The colonization of microbes on MPs would significantly alter their transport behavior, i.e., buoyancy, in fresh water. In this research, we studied the effects of biofilm colonization on the sinking and floating of three MPs, i.e., polyethylene terephthalate (PET), polypropylene (PP), and polyvinyl chloride (PVC), after 44 days of incubation in three freshwater systems (the Niushoushan River, the Qinhuai River, and East Lake) in China. The results showed that the biofilms attached to the three MPs contained different biomass and chlorophyll-a levels were related to water environmental conditions and physicochemical properties of MPs, based on redundancy analysis. Generally, PET and PVC sinking, with density higher than water, tended to increase after biofilm formation. Thereafter, the settling velocity of biofouled PET and PVC squares became faster than that of the virgin ones. In summary, our study suggested that biofouling does affect the sinking of MPs in fresh water and consequently influences the transport behavior and the distribution characteristics of MPs in freshwater environments, and this issue deserves more scientific attention.

PEI-capped KMgF3:Eu2+ nanoparticles for fluorescence detection of nitroaromatics in municipal wastewater.

The probing and quantitative detection of nitroaromatics is key for public safety and the monitoring of wastewater. Currently, most techniques used for the detection of nitroaromatics require ideal conditions rather than real conditions, making practical applications challenging. As nitroaromatics have strong absorption in the range of 350-370 nm, we can design a kind of KMgF3:Eu2+ nanophosphor with a strong f-f transition emission located at 362 nm, and an energy resonance transfer system based on the overlap of the emission peak of nanophosphors and the absorption peak of nitroaromatics can be constructed to realize the quantitative detection of nitroaromatics in municipal wastewater. Based on this, in this paper, a fluorescence resonance energy transfer (FRET) sensor is designed by choosing polyethylenimine (PEI)-capped KMgF3:Eu2+ nanoparticles as an energy donor for the ultrasensitive detection of nitroaromatics, which can also work as an energy acceptor. The KMgF3:Eu2+ nanoparticle sensor shows great sensitivity and selectivity and good linear characteristics in both DI water and wastewater. The detection limits in municipal wastewater were 0.456, 0.598, 0.667, 0557 and 0.678 ng/mL for TNT, TNP, p-nitrotoluene, dinitrobenzene (DNB), and nitrobenzene (NB), respectively. The detection accuracy was identified by high-performance liquid chromatography (HPLC). The results showed that the sensor had superior sensitivity and great accuracy and could be used in practical applications.

Distinct microbial metabolic activities of biofilms colonizing microplastics in three freshwater ecosystems.

Concerns are growing about the increasing amounts of microplastics (MPs) and their ecological impacts, especially the influences of "plastisphere" in the freshwater ecosystems. Although the microbial structure and composition of biofilms are investigated, knowledge of their microbial functions remains limited. Herein, we investigated the functional diversity of carbon metabolism in biofilms colonizing one inert (glass) and two MPs as polyvinyl chloride (PVC) and polyethylene terephthalate (PET) substrates incubated for 44 days in situ in the Niushoushan River, the Qinhuai River, and Donghu Lake. 2D confocal laser scanning microscopy images visualized distinct micro-structures and biofilm compositions on three substrates. BIOLOG ECO microplates indicated variation on carbon utilization capacities of biofilms of inert and MPs in three freshwater ecosystems. Biofilms on PET showed lower capacities and carbon metabolism rates than those on glass and PVC, indicating the presence of substrate-specific functional diversity. The Shannon-Wiener diversity, Simpson diversity and Shannon evenness indices for the Niushoushan River and Donghu Lake were ordered as glass > PVC > PET. Besides to MPs-specific factors, environmental factors including nutrient (i.e., TN and TP) and turbidity largely shaped biofilm carbon metabolism. Overall findings demonstrated that as specific niches, MPs influenced microbial-mediated carbon cycling in the freshwater ecosystems and MPs-promoted microbial communities posed ecological significance.

Transport behavior of micro polyethylene particles in saturated quartz sand: Impacts of input concentration and physicochemical factors.

The long-term contamination of soil by microplastics may pose risks that are often still not well understood, and the ecological effects of microplastics are mainly dependent on their environmental behavior in environments. This study used saturated quartz sand as a solid porous medium to study the migration and influencing factors of 40-48 µm polyethylene (PE) particles in saturated porous media. The breakthrough curves at different injection concentrations (0.3, 0.4, 0.5 mg/L), flow rates (1.0, 1.5, 2.0, 2.5 ml/L), porous medium particle sizes (1-2, 2-4 mm), ionic strengths (0, 0.01, 0.05 mol/L) and concentrations of fulvic acid (FA) (0, 5, 10 mg/L) were compared and analyzed. The Derjaguin-Landau-Verwey-Overbeek (DLVO) theory was used to more accurately explain relevant transport behaviors. The results showed that the input concentration, flow rate, and particle size can affect the migration of PE particles individually or in combination. As ionic strength increased, the repulsion between microplastics and quartz sand gradually disappeared according to DLVO theory, and their attraction gradually strengthened. As a result, fewer microplastics could penetrate the sand column and reach the water body. With the continuous addition of FA, the repulsive energy between microplastics and quartz sand rose from DLVO theory, and the migration ability of microplastics initially increased before becoming stable because of the effect of straining. In all cases, the migration ability of PE was low (C/C0 < 0.35), and most PE particles remained in the porous media during the whole experimental periods. This study provides new insights of understanding the migration of microplastics in environment.

Microbial carbon metabolic functions of biofilms on plastic debris influenced by the substrate types and environmental factors.

As an artificial type of microbial carrier, plastic debris has been widely detected in freshwater habitats, and the potential impacts of the plastisphere (biofilms colonized on plastics) in aquatic ecosystems have drawn increasing attention. Distinct community compositions and structures of biofilms in plastic and natural substrates have been recorded in freshwater environments. However, the microbial metabolic functioning of the plastisphere was underestimated, especially in freshwater environments. In this study, the effects of substrate types on the carbon metabolic functions of biofilms were studied by in situ cultivation of biofilms on plastics (polyvinyl chloride, PVC and polyethylene, PE) and natural substrate (cobblestone) for 44 days in two rivers (the Niushoushan River and the Qinhuai River) and two lakes (Donghu Lake and Xuanwu Lake). Biofilms on plastics showed higher biomasses than those on natural substrates in all ecosystems. Variations in the micro-structure and compactness of biofilms developed under different substrates were observed from scanning electron microscope and confocal laser scanning microscope image analyses. The carbon metabolic activities of the biofilms evaluated by BIOLOG EcoPlate were different between plastics (PVC and PE) and natural substrate (cobblestone) in the four freshwater ecosystems. In the Niushoushan River, PE-associated biofilms had different capacity in using carbon sources from cobblestone-associated biofilms as illustrated by the Shannon-Wiener diversity index and Shannon evenness index. Additionally, the metabolic functional diversity profiles of biofilms on PVC were significantly different from those on cobblestone in the other three aquatic ecosystems. Moreover, results from variation partitioning analysis suggested that the impact of environmental factors (contribution: 21%) on microbial carbon metabolic functions was much greater than that of substrate types (contribution: 6%). These findings illustrated distinct microbial functions of biofilms inhabited on plastics, and environmental factors play a decisive role in the differentiation and specificity of carbon metabolism of the plastisphere. This study offers new insights that plastics serving as artificial microbial niches have the ability to affect the microbial-mediated carbon cycling process in aquatic ecosystems.

Distinct community structure and microbial functions of biofilms colonizing microplastics.

Microplastics are frequently detected in freshwater environments, serving as a new factitious substrate for colonization of biofilm-forming microorganisms. Distinct microbial assemblages between microplastics and surrounding waters have been well documented; however, there is insufficient knowledge regarding biofilm colonization of plastic and non-plastic substrates, despite the fact that microbial communities generally aggregate on natural solid surfaces. In this study, the effects of substrate type on microbial communities were evaluated by incubation of biofilms on microplastic substrates (polyethylene and polypropylene) and natural substrates (cobblestone and wood) for 21 days under controlled conditions. Results from high-throughput sequencing of 16S rRNA revealed that the alpha diversity (richness, evenness, and diversity) was lower in the microplastic-associated communities than in those on the natural substrates, indicating substrate-type-coupled species sorting. Distinct community structure and biofilm composition were observed between these two substrate types. Significantly higher abundances of Pirellulaceae, Phycisphaerales, Cyclobacteriaceae, and Roseococcus were observed on the microplastic substrates compared with the natural substrates. Simultaneously, the functional profiles (KEGG) predicted by Tax4Fun showed that the pathways of amino acid metabolism and metabolism of cofactors and vitamins were increased in biofilms on the microplastic substrates. The findings illustrate that microplastic acts as a distinct microbial habitat (compared with natural substrates) that could not only change the community structure but also affect microbial functions, potentially impacting the ecological functions of microbial communities in aquatic ecosystems.

An eximious and affordable GSH stimulus-responsive poly(α-lipoic acid) nanocarrier bonding combretastatin A4 for tumor therapy.

Due to poor penetration of cytotoxic-drug-loaded-nanomedicines, more and more attention has been paid to nanodrugs of vascular disrupting agents (VDAs). However, traditional VDA nanodrugs lack tumor-selectivity, so new nano-carriers for tumor-selective CA4 delivery are urgently needed. Here, a novel PEGylated poly(alpha-lipoic acid) graft combretastatin A4 (PALA-g-mPEG/CA4) nanoparticle with glutathione (GSH) stimulus responsive ability was prepared from alpha-lipoic acid in a simple approach, which can accumulate and release CA4 selectively in a tumor site. Furthermore, this simple system has potential application value for tumor-targeting delivery and GSH sensitive release of other drugs.

Effects of Nanoplastics on Freshwater Biofilm Microbial Metabolic Functions as Determined by BIOLOG ECO Microplates.

Nanoplastic (NP) contamination is becoming a pervasive issue as NPs, originating from microplastic particles, pose potentially harmful environmental impacts on aquatic ecosystems. The environmental hazards of NPs on microorganisms have been well documented in recent studies; however, little is known about their ecotoxicity effects on freshwater biofilms, which serve as important primary producers and decomposers and are highly connected with other ecosystem components. We investigated the effects of NPs on the microbial metabolic functions of freshwater biofilms in terms of carbon source utilization ability. Biofilm samples were collected, cultivated in a hydrodynamic flume for six weeks, and then exposed in polystyrene (PS) beads (100 nm in size) with different NP concentrations (1, 5, and 10 mg/L). BIOLOG ECO microplates were used to quantify carbon source utilization characteristics. The data were analyzed using average well-color development (AWCD), functional diversity indices, and principle component analysis (PCA). Results showed that the total carbon metabolic functions (represented by AWCD) remained constant (p > 0.05) with elevated NP concentrations, but some specific carbon sources (e.g., esters) changed in their utilization ability (p < 0.05). The microbial functional diversity (Shannon-Wiener diversity index, Simpson diversity index, and Shannon evenness index) was significantly reduced under 10 mg/L NPs (p < 0.05), indicating an inhibiting effect of NPs on biofilm metabolic diversity. This study examined NP ecotoxicity effects on microbial metabolic activities at the community level, but further studies are required to fully understand the mechanisms driving this change.

Acute effects of nanoplastics and microplastics on periphytic biofilms depending on particle size, concentration and surface modification.

Microplastics (MPs) can disintegrate into smaller sized microplastics and even nanoplastics (NPs). The toxicity of nanoplastics and microplastics on freshwater organisms have been well explored recently, however, very little is known about the potential impacts of NPs on freshwater biofilms, which are essential for primary production and nutrient cycling in aquatic ecosystems. In this study, we studied the acute effects (3 h of exposure) of polystyrene beads (PS, with diameter range from 100 nm to 9 µm) on five biological endpoints targeting community and ecosystem-level processes in biofilms: chlorophyll a, photosynthetic yield, and three extracellular enzyme activities. The results showed that the large size PS beads (500 nm, 1 µm, and 9 µm) exhibited negligible effects on the determined biological endpoints in biofilms within the range of concentrations (5-100 mg/L) in this study. However, high concentration of PS beads (100 nm, 100 mg/L) significantly decreased the content of chlorophyll a, and the functional enzyme activities of ß-glucosidase and leucine aminopeptidase, suggesting negative effects on the carbon and nitrogen cycling of freshwater biofilms. Moreover, the influences of PS NPs (100 nm) on biofilms strongly depended on the surface modification of PS particles, with the positively charged PS NPs (amide-modified) exhibiting the highest toxicity to biofilms. The excess generation of reactive oxygen species (ROS) in this study indicated oxidative stress induced by PS NPs, which might lead to the observed nano-toxic effects on biofilms. In response, the antioxidant activity of biofilm was enhanced as indicated by the increased total antioxidant capacity (T-AOC). Overall, our findings highlight nanoplastics have potential to disrupt the basic ecological functions of biofilms in aquatic environments.

Effects of CeO2, CuO, and ZnO nanoparticles on physiological features of Microcystis aeruginosa and the production and composition of extracellular polymeric substances.

Extracellular polymeric substances (EPS) are key components of the cyanobacterium Microcystis aeruginosa and play an important role in cyanobacteria blooms formation. Here, we analyzed the effects of 48-h exposure to nanosized CeO2 (n-CeO2), CuO (n-CuO), and ZnO (n-ZnO) on the production and composition of EPS of M. aeruginosa. Toxicity experiments revealed that soluble nanoparticles (NPs) (n-ZnO, n-CuO) demonstrated higher toxicity to cells and caused membrane damage. The production of LB-EPS increased by 34.48, 20.09, and 46.33 %, and TB-EPS increased by -5.78, 22.3, and -2.67 % in the presence of n-CeO2, n-CuO, and n-ZnO NPs, respectively, and polysaccharides are the main incremental portion compared with protein and humic acids. Three-dimensional excitation-emission fluorescence spectra revealed the enhancement of fulvic-humic-like and disappearance of tyrosine aromatic substances in TB-EPS compared with the slight changes observed in LB-EPS. Fourier-transform infrared spectroscopy illustrated the susceptibility of -NH2 and double-bonded carbon and oxygen in amides to three types of NPs. These results improve our understanding of the potential influence of NPs on the aggregation behaviors of cyanobacteria and formation process of cyanobacteria blooms. Graphical abstract ᅟ.

Transport and long-term release behavior of polymer-coated silver nanoparticles in saturated quartz sand: The impacts of input concentration, grain size and flow rate.

This study investigated the transport and long-term release of stabilized poly vinylpyrrolidone-coated silver nanoparticles (PVP-AgNPs) in a quartz sand column with various sand grain sizes (0.3-0.5 µm, 0.5-1.0 µm, 1.0-2.0 µm), input concentrations of PVP-AgNP solution (1, 5, 15, 25 mg/L), and flow rates corresponding to a filter velocities (1.0, 1.5, 2.0, 2.5 mL/min-0.14, 0.21, 0.28, 0.35 cm/min) by determining breakthrough curves, retention profiles, and long-term release curves. Breakthrough curves and retention profiles were simulated by a mathematical model based on the advection dispersion equation coupled with second-order kinetics. The increased transport of PVP-AgNPs in quartz sand occurred with increased grain sizes and reduced input concentrations, and the transport can be predicted by the colloid filtration theory and DLVO theory. The long-term (one week) release amounts of retained PVP-AgNPs were 42.78%, 31.45%, and 10.95% in the fine, medium, and coarse sand columns, respectively, and were 34.70%, 40.79%, 47.24%, and 57.32% at flow rates of 0.0363, 0.0436, 0.0545, and 0.0726 mL/min, respectively. The released quantity of retained PVP-AgNPs decreased as the sand grain size increased. This phenomenon is opposite with the trend of increased transport of PVP-AgNPs with increased grain size in the transport test, which most likely because colloidal filtration regulates the transport process and adsorption (and desorption) dominates the release process. Increasing the flow rate increased the shear force on the particles, which improved the release of PVP-AgNPs. The results of the release tests further verified our previous published studies showing that the long-term release of retained PVP-AgNPs in the quartz sand was mostly in the form of released nanoparticles rather than ions. The results of this study indicated that sand grain size, input concentration, and flow rate have a prominent influence on the transport and long-term release behavior of PVP-AgNPs in saturated quartz sand.

Transport, retention, and long-term release behavior of polymer-coated silver nanoparticles in saturated quartz sand: The impact of natural organic matters and electrolyte.

This study investigated the transport and long-term release of stabilized silver nanoparticles (AgNPs), including polyvinylpyrrolidone-coated AgNPs (PVP-AgNPs) and bare AgNPs (Bare-AgNPs), in the presence of natural organic matters (NOMs; both humic acids (HA) and alginate (Alg)) and an electrolyte (Ca2+) in a sand-packed column. Very low breakthrough rate (C/C0) of AgNPs (below 0.04) occurred in the absence of NOM and the electrolyte. Increasing the concentration of NOM and decreasing the influent NOM solution's ionic strength (IS) reduced the retention of AgNPs. The reduced NP retention at high NOM and low IS was mainly attributed to the increased energy barrier between the AgNPs and the sand grain surface. Notably, the retention of PVP-AgNPs was enhanced at high Alg concentration and low IS, which mainly resulted from the improved hydrophobicity that could increase the interaction between the PVP-AgNPs and the collector. The total release amount of PVP-AgNPs (10.03%, 9.50%, 28.42%, 6.37%) and Bare-AgNPs (3.28%, 2.58%, 10.36%, 1.54%) were gained when exposed to four kinds of NOM solutions, including deionized water, an electrolyte solution (1 mM Ca2+), HA with an electrolyte (1 mM Ca2+), and a Alg (40 mg/L) solution with an electrolyte (1 mM Ca2+). The long-term release of retained silver nanoparticles in the quartz sand was mostly through the form of released Ag NPs. The factors that increased the mobility of AgNPs in quartz sand could improve the release of the AgNPs. The release of AgNPs had no significant change in the presence Ca2+ but were increased in the presence of HA. The Alg slightly decreased the release of AgNPs by increasing the hydrophobicity of AgNPs. The results of the study indicated that all the tested NOM and Ca2+ have prominent influence on the transport and long-term release behavior of silver nanoparticles in saturated quartz sand.