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Microplastic (MP) biofilms with heterogeneous bacterial compositions and structure have become a hotspot of antibiotic resistance genes (ARGs) in aquatic environments. The evolutionary features of ARGs and their related factors including class 1 integron (intI1), metal resistance genes (MRGs), and bacterial communities in MP biofilms under exogenous pressures and how they compared with natural substrates (NS) are unclear. The individual and combined pressures of sulfamethoxazole, tetracycline, and zinc were used to drive the dynamic evolution of ARGs, intI1, MRGs, and bacterial communities in the MP and NS biofilms. The exogenous pressures from the combined selection of sulfamethoxazole, tetracycline, and zinc and their increasing concentrations both significantly enhanced the abundances of ARGs on the MP compared to the NS. Meanwhile, the selective pressures resulted in obvious dissimilarities between the MP and NS bacterial communities. The core bacterial taxa and the co-occurrence patterns of ARGs and bacterial genera in the biofilms of MP and NS were obviously different, and more potential ARG host bacteria selectively colonized the MP. Metal pressure also enhanced the enrichment of ARGs in the MP biofilms by promoting the spread of intI1 via the co-selection mechanism.Organic films were widely found on indoor impermeable surfaces exposed to gaseous organic compounds, but few studies have addressed the film growth details on different indoor substrates. In this study, we observed the topography evolution of phthalic acid ester (PAE) organic films on three impermeable substrates polished glass (G-P), mirror-polished stainless steel (SS-M) and drawn stainless steel (SS-D). PAE organic films were preferentially formed upon the flat surface with sparse inherent nano-peaks of substrate G-P and in valleys of substrate SS-M and SS-D. Surface uniformity of substrates and viscosity of PAE molecules were inferred as critical parameters determining the surface average adhesion forces. We obtained the partition coefficients of DEP, DnBP, BBP and DEHP on substrate G-P, SS-M and SS-D by fitting the initial monolayer adsorption process. Organic films continuously grew instead of reaching adsorption equilibrium after long-term PAE exposure, indicating that multilayer adsorption may occur. The organic film growth rates in saturated gas-phase PAE concentrations were quantified as about one-tenth of the results in previous studies where substrates were simultaneously exposed to multiple pollutants. To sum up, the results outline PAE adsorption details on impermeable materials and provide a reference for better estimation on PAE exposure assessment.Contaminants of emerging concern (CEC) are a focus in marine protection. Several CECs are released with wastewater effluents to coastal environments and their offshore occurrence has been recently documented. Routine monitoring is key for implementing marine protection acts, however infrastructural, financial, and technical limitations hinder this task along broad spatial transects. Here we show the efficacy of a new infrastructure enabling unmanned sampling of surface water from ships of opportunity in providing reliable and cost-effective routine monitoring of CECs along a Europe-Arctic transect. The distribution and long-range transport of several pharmaceuticals and personal care products, artificial food additives, and stimulants were assessed. Validation of operations through strict procedural and analytical quality criteria is presented. A framework to estimate a compound-specific spatial range (SR) index of marine long-range transport based on monitoring results and information on source spatial distribution, is introduced. Estimated SR values ranged 50-350 km depending on compound, yielding a ranking of long-range transport potential which reflected expectations based on degradation half-lives. SR values were used to calculate prior maps of detection probability that can be used to plan future routine monitoring in the region.Herein, novel 3D hollow-carved Co2C-doped CoAl2O4 fiber composites (3D-CA-FC) were successfully synthesized via a simple-green pyrolysis method and exhibited remarkably outstanding elimination performance for tetracycline (TC) by adsorption and degradation. The results indicated that the TC adsorption process of the samples could be accurately described by the pseudo-second-order and Langmuir isothermal model, and the maximum TC uptake reached up to 1889.63 mg/g under neutral conditions. Meanwhile, 3D-CA-FC showed good affinity for TC and its adsorption capacity was greatly promoted due to the presence of humic acid, CO32- ion and weakly alkaline environment. About complete degradation of TC could be completed within 60 min under suitable conditions. A significant improvement of catalyst rate was observed after the addition of CO32- ion, because of the selective degradation of CO3•- to TC. BET, XPS and FT-IR analysis indicated that the mechanisms of TC uptake can be ascribed to pore-filling, H-bonds and complexation. Radical trapping experiments showed that 1O2 should serve as predominant contributions, and SO4•- and •OH also played a role in the degradation process. This study provides some inspiration for the construction of 3D-CA-FC as a novel and promising bifunctional material for the elimination of contaminants in water treatment.A key matter in heavy metal removal technology is to develop the adsorbents with efficient adsorption sites. In this study, an oxygen-rich covalent organic framework (JUC-505) was functionalized by carboxyl (-COOH) groups to form synergetic effects aiming for the removal of Cd(II) and Pb(II) ions. JUC-505-COOH shows a high Cd(II) uptake of 504 mg⋅g-1 surpassing most of the reported porous adsorbents. Meanwhile, the kinetics study shows a rapid adsorption process at a high initial concentration (100 mg⋅L-1), and the equilibrium can be reached within 5 min. We investigated the adsorption mechanism in-depth by density functional theory calculations, proving the synergistic effects of surface complexation and hydrogen-bond, which are from the post-modified -COOH groups and the in-situ oxygen atoms of JUC-505, respectively. Moreover, under the interference of common ions in natural water, the removal efficiency of Cd(II) is almost insusceptible, which sheds lights on the potential for the application in the natural water purification. In addition, the Pb(II) uptake (559 mg⋅g-1) and the adsorption kinetics also surpass most of the reported porous adsorbents.Quantification of polychlorinated dibenzo-p-dioxins (PCDDs) and polychlorinated dibenzofurans (PCDFs) is a requirement of the Stockholm Convention on persistent organic pollutants (POPs), and essential to evaluate and understand their environmental fate and associated health risks. Unfortunately, works estimating the emission of PCDD/Fs in China are limited, especially in terms of historical trends and information on spatial distribution. In this study, provincial emissions of 17 toxic PCDD/Fs congeners from 79 sources were quantified from 1960 to 2014, and 0.1º × 0.1º gridded emissions for 2014 were obtained by applying a source-specific, annually varying emission factor (EF) dataset with similar time trends as measurements for China. Historical national PCDD/F emissions showed an increasing trend until around 1980, and then plateaued due to decreased emissions from cement production and waste burning. Decreased emissions from cement production and waste burning in northeast, east, and south China, and Taiwan province were the main causes for the stabilized national emissions after 1980. Spatially, highly positive correlations of emission densities with population and GDP densities were identified, but no clear temporal patterns were observed. Emission densities showed a decreasing trend in the order of cities, towns and rural areas, while the opposite was seen for per capita emissions.Since Stockholm Convention listed polybrominated diphenyl ethers (PBDEs) as persistent organic pollutants and banned their addition, alternative halogen flame retardants (AHFRs) have been substituted for PBDEs. This study systematically investigates the change trends of PBDEs and AHFRs from typical e-waste plastics and dust, as well as clarifying human exposure risks of PBDEs in formal and informal e-waste recycling enterprises, repair store and residential building. The results show that the PBDEs levels in five typical types of e-waste vary in the range of 1.08 × 10-3-30.8 μg/g, meeting the requirements of RoHS regulation. Compared with the residential buildings (1.49-1.68 μg/g), PBDEs in the dust from the formal and informal e-waste recycling enterprises are much higher, ranging from 4.70 to 536 μg/g. [https://www.selleckchem.com/JAK.html JAK cancer] BDE-209 is the main congener in most e-waste plastic and dust samples. Meanwhile, AHFRs have become the important composition (3.5-61.5%) in e-waste plastics, while its contribution is lower in dust, implying the higher enrichment efficiency of PBDEs. For PBDEs exposure, the dust intake risk of PBDEs is much higher than skin contact for the workers, and the highest hazard quotient (HQ) value (1.40 × 10-1) and cancer risk (CR) value (1.21 × 10-7) both imply safe exposure levels.Previous research has been demonstrated that the residual unextracted antibiotics in spiramycin fermentation residue (SFR) could be efficiently removed by thermally activated peroxodisulfate (TAP) pretreatment, indicating the improvement of biodegradability. This study aimed to investigate the effect of TAP pretreatment on the succession of bacterial community and fate of antibiotic resistance genes (ARGs) during SFR composting. Results indicated that TAP pretreatment increased the composting temperature and promoted the decomposition of organic matters. Furthermore, TAP pretreatment could increase bacterial alpha diversity and significantly reduce the relative abundance of ARGs (1.13-1.75 times) and mobile genetic elements (MGEs) (1.13-1.32 times) after composting. The compost of pretreated SFR by TAP could reduce the enrichment of ARGs and MGEs in the bacterial community, especially the rRNA methylase genes of ermB (4-142-folds). Redundancy analysis showed that Actinobacteria, Bacteroidetes, Proteobacteria and horizontal gene transfer mediated by MGEs (intI1) was positively related to the changes in ARGs (accounted for 97.4%). Network analysis showed that Firmicutes was the main bacterial hosts of ARGs and MGEs. These findings demonstrated that TAP pretreatment combined composting was a promising strategy for SFR safe treatment and disposal that could reduce the proliferation and transfer of ARGs.Uranium (U) immobilization from wastewater by zero valent iron (ZVI) was widely concerned through reduction and surface adsorption. Releasing of U due to re-oxidation of U(IV) into U(VI) limited the application of ZVI in U decontamination. In this work, a kind of biochar supported nano zero valent iron (Fe/BC(900)) was obtained by carbothermal reduction of starch mixed with ferric nitrate at 900 °C. U immobilization behavior by Fe/BC(900) in the presence of phosphate (P) was investigated. The U immobilization reaction was adjusted by controlling the sequence of U, Fe/BC(900) and P. U immobilization efficiency was enhanced to 99.9% in the presence of P. Reaction sequence of U, Fe/BC(900) and P influenced the U immobilization efficiency, which followed the order of (U-P)+Fe/BC(900)&gt;(U- Fe/BC(900))+P&gt;U+Fe/BC(900)&gt;(P-Fe/BC(900))+U. P and nZVI both contributed to enhancing U immobilization through precipitation of uranyl-P and reductive co-precipitate (U(IV)) in a wide pH range. The released Fe ions could precipitate with uranyl and phosphate.