Enhanced Antibacterial Activity against Escherichia coli Based on Cationic Carbon Dots Assembling with 5-Aminolevulinic Acid.

Carbon dots (CDs) with positive surface charges are considered one of the encouraging nanomedications for antibacterial applications. However, due to the distinctive membrane structure of Gram-negative bacteria, cationic CDs with relatively high concentrations are usually required for effective treatment, which might bring out serious safety issues at high doses. Therefore, it is of substantial significance to improve the killing efficiency of cationic CDs on Gram-negative bacteria at appropriately low concentrations. In this work, optimized cationic CDs (bPEI25 000-CDs) were prepared via a hydrothermal method with citric acid and branched PEI25000, which offered a positive surface potential, elimination abilities against Escherichia coli, and relatively high biosafety. The optimized bPEI25 000-CDs can further assemble with the clinical photodynamic therapy (PDT) drug 5-aminolevulinic acid (5-ALA) through electrostatic interaction. Moreover, compared with bPEI25 000-CDs and 5-ALA, the bacterial survival rate was significantly reduced by the ALA-bPEI25 000-CD-induced PDT effect. Even when the dose of bPEI25 000-CD carrier was halved, the bacterial survival could be reduced by 44.4% after light exposure compared to those incubated in the dark. The investigation of the bacterial morphology, membrane potential, and intracellular ROS production suggested that the enhanced antibacterial activity may be due to the membrane dysfunction and cell damage resulting from the high interaction between positively charged ALA-bPEI25 000-CDs and the bacterial cell membrane. Meanwhile, the cationic ALA-bPEI25 000-CDs may facilitate the cellular uptake of 5-ALA, resulting in a more efficient PDT effect. In summary, the antibacterial strategy proposed in this study will provide a novel approach for expanding the application of CD-based nanomedications.

Study on the therapeutic effect of glucocorticoids on acute kidney injury in rats exposed to diquat.

AIMS: To preliminarily explore, whether glucocorticoids have a therapeutic effect on diquat-induced acute kidney injury in rats. METHOD: 150 Wistar rats were randomly divided into six groups: exposure model group (DQ group), dexamethasone control group (GC group), blank control group (Ctrl group), dexamethasone 2.1 mg/kg dose group (DQ+L-GC group), dexamethasone 4.2 mg/kg dose group (DQ+M-GC group), and dexamethasone 8.4 mg/kg dose group (DQ+H-GC group), with 25 rats in each group. Each group was further divided into five subgroups, 24 h, 3 d, 7 d, 14 d, and 21 d after exposure, according to the feeding time and the course of treatment, with five animals in each subgroup. The rats in DQ, DQ+L-GC, DQ+M-GC, and DQ+H-GC groups were administered 115.5 mg/kg diquat by gavage, respectively. Moreover, 30 min after gavage, rats in DQ+L-GC group, DQ+M-GC group, DQ+H-GC group and GC group were intragastric administered dexamethasone 2.1 mg/kg, 4.2 mg/kg, 8.4 mg/kg and 8.4 mg/kg, respectively. After 7 days, the intraperitoneal injection of dexamethasone was changed to 6.3 mg/kg prednisone by intragastric administration. Subsequently, 7 days later, it was changed to 3.15 mg/kg prednisone by intragastric administration until the end of the experiment on 21 days. After the start of the experiment, changes in the conditions of the rats in each group were observed at a fixed time every day, changes in the body weight of the rats were monitored at the same time, and the death of the rats was recorded at 24 h, 3 d, 7 d, 14 d, and 21 d after exposure. The rats were sacrificed by an intraperitoneal injection of 100 mg/kg sodium pentobarbital overdose. Blood was collected by puncture of the inferior vena cava, used to determine Cr and BUN. The upper segment of the left kidney was collected for histopathological examination. Elisa was used to detect neutrophil gelatinase-associated lipocalin (NGAL) and kidney injury molecule-1 (KIM-1) in the lower segment of left kidney. TLR4, Myd88, and NF-κB were detected in the right kidney. RESULTS: (1) After exposure, most rats in DQ group, DQ+L-GC group, DQ+M-GC group and DQ+H-GC group showed shortness of breath, oliguria, diarrhea, yellow hair and other symptoms. No symptoms and related signs were observed in Ctrl group and GC group. (2) The weight of rats in the Ctrl group and the GC group increased slowly during the test. the body weight of the rats in the DQ, DQ+L-GC, DQ+M-GC, and DQ+H-GC groups continued to decrease after self-infection. Body weight dropped to the lowest point at approximately 7 d, and gradually increased from 7 d to 21 d. (3) A small amount of capillary congestion in the medulla was observed after 7 days in the GC group. The DQ group showed tubular atrophy, edema of the epithelial cells, and over time, the tubules were seen dilated and became irregular in shape; large amount of capillary congestion was also observed in the renal cortex and medulla. The renal injury in the DQ+L-GC group was less than that in the DQ group. DQ+H-GC group had no obvious injury before 7 d, but more renal tubules were seen in the DQ+H-GC group from 7 d to 14 d. (4) Compared with the DQ group, there was no difference before 14 d, and at 14 d-21 d, DQ+L-GC group, DQ+M-GC group, DQ+H-GC group all had different degrees of decline. NGAL content: Compared with the DQ group, the content of NGAL and KIM-1 in kidney tissue of the DQ+L-GC, DQ+M-GC, and DQ+H-GC groups decreased compared with the DQ group at each time node. (5) Compared with the Ctrl group, the expression of TNF-α, TLR4, MyD88, NF-κB in the DQ, DQ+L-GC, DQ+M-GC, and DQ+H-GC groups at each time node increased in the renal tissue. The content of TNF-α, TLR4, MyD88, NF-κB in kidney tissue of the DQ+L-GC, DQ+M-GC, and DQ+H-GC groups at each time node was lower than that in the DQ group. CONCLUSION: (1) Diquat can cause kidney damage in rats, mainly manifested as renal tubular atrophy, epithelial cell edema, capillary congestion and dilation, and the renal function damage indicators have been improved to varying degrees. (2) Glucocorticoids have therapeutic effects on acute kidney injury in rats exposed to diquat. During the treatment, the efficacy of glucocorticoids did not increase with increasing doses after reaching a dose of 4.2 mg/kg. (3) TLR4 receptor-mediated TLR4/Myd88/NF-κB signaling pathway is involved in the inflammatory response of acute kidney injury in diquat poisoning rats. Glucocorticoids can inhibit the inflammatory response, thereby affecting the expression of TLR4/Myd88/NF-κB signaling pathway-related proteins.

Chlorinated paraffins in multimedia during residential interior finishing: Occurrences, behavior, and health risk.

Though with bioaccumulation and toxicity, chlorinated paraffins (CPs) are still high produced and widely utilized in various daily necessities for extender plasticization and flame retardation. CPs can be released during the reprocessing processes of finishing materials and distributed in multi-environmental media. Herein, concentrations and compositions of CPs in four representative media including interior finishing materials, PM10, total suspended particulate (TSP), and dust samples collected from eight interior finishing stages were studied. Unexpectedly, CP concentrations in ceramic tiles was found to be high with a mean value of 7.02 × 103 µg g-1, which could be attributed to the presence of CPs in the protective wax coated on ceramic tiles surfaces. Furthermore, the pollution characteristics of short-chain and medium-chain CPs (SCCPs and MCCPs) in those samples were inconsistent. According to the investigation regarding Kdust-TSP and [Formula: see text] , the occurrence and distribution of CPs in indoor atmospheric particles (PM10 and TSP) and dust were highly affected by reprocessing processes (cutting, hot melting, etc.) compared to that in the finishing materials. Moreover, dermal contact was the primary pathway of CP exposure for the occupational population (interior construction workers) for most interior finishing stages, and the interior finishing process is the prime CP exposure period for the occupational groups. As suggested by our assessment, though hardly posing an immediate health risk, CPs exposure still presents unneglected adverse health effects, which calls for adequate personal protections during interior finishing, especially in developing countries.

Case report: Methemoglobinemia caused by nitrobenzene poisoning.

Nitrobenzene poisoning is uncommon, with most cases occurring in the dye, paint, and other chemical industries. Nitrobenzene enters the body mainly through the skin, respiratory tract, and oral cavity. Nitrobenzene poisoning symptoms include hypermethemoglobinemia, hemolytic anemia, liver and kidney dysfunction, cardiogenic pulmonary edema, and toxic encephalopathy, which endanger people's lives. Therefore, we present a case of nitrobenzene poisoning caused by skin absorption, focusing on its clinical characteristics and treatment outcomes. A 58 years-old man presented to our department with confusion and cyanosis. He has a history of hypertension and cerebral infarction. The patient was diagnosed with moderate occupational acute benzene poisoning with nitro compounds. Symptomatic support, methylene blue, and other antioxidant treatments were commenced after diagnosis. After treatment, the patient's condition gradually improved, and he was discharged.

The neglected potential source of microplastics from daily necessities: A study on protective mobile phone cases.

Microplastics (MPs) pollution has become a serious global environment problem. It is therefore of practical significance to investigate the MP pollution caused by using plastic materials on a daily basis. In this study, different protective mobile phone cases (PMPCs) were selected as a representative plastic commodity that are in contact with the human body for long periods to explore the generation and transportation of MPs during 3 months of actual use. The average abundances were 1122 particles cm-2 on the PMPC and 314 particles cm-2 on the palm, respectively. There were four main kinds of MPs produced during the use of different PMPCs, which indicated that waste plastics may be recycled and used as raw materials, resulting in a complex PMPC composition. The median sizes of MPs on the surfaces of PMPCs and palms were 28 and 32 µm, respectively, which were smaller than the sizes reported in other studies. The combined effect of ultraviolet ageing and friction was the main reason for MP generation during daily PMPC use. Based on the results of a fitted regression equation and Monte Carlo simulation, the sharply generation of MPs may occur when PMPC was used for approximately 33 days.

The impact of three related emission industries on regional atmospheric chlorinated paraffins pollution.

Identifying the contributions of various chlorinated paraffins (CPs) sources in the environment plays an important practical role in the prevention and control of the CPs contamination. However, little is known about how main CP-related emission industries affect the regional atmospheric characteristics of CPs, including CP products industry, metal working industry, and polyvinyl chloride (PVC) industry. In this study, 60 passive air samples were collected from five typical cities in Henan Province, China, which had serious CP pollution and different structures of CP-related emission industry. Short chain CPs (SCCPs) and medium chain CPs (MCCPs) were detected in all samples in concentrations ranging of 2.6-7.7 × 102 and 2.1-4.3 × 102 ng m-3, respectively, which were higher than those in most reports. Moreover, Luoyang (LY) is different from other cities, showing a relatively severe MCCP contaminations. The CP pollution characteristics between different cities are obviously affected by the proportion of local CP-related industries. According to the results of cluster heatmaps, the local CP-related emission industrial structure had a greater impact on MCCPs pollution than SCCPs. Additionally, the contribution of metal working industry was beyond that of PVC production industry and CP products industry.

Perfluoroalkyl acids in dust on residential indoor/outdoor window glass in Chinese cities: occurrence, composition, and toddler exposure.

The dust on indoor and outdoor surfaces of the window glasses were collected using sterile cotton balls in 11 cities from China. Two sampling campaigns were conducted with the time interval of 7 days to investigate the accumulation especially during the Spring festival holidays. Twenty-nine perfluoroalkyl acids (PFAA) were quantified to investigate concentration, composition, and toddlers' exposure. The concentrations of ∑PFAA ranged from no detection (nd) to 43 ng/m2 (mean 8.9 ± 10 ng/m2). Perfluorobutanoic acid (PFBA) was detected in 78% samples and accounted for 55 ± 21% of ∑PFAA concentrations. 6:2 fluorotelomer sulfonic acid (6:2 FTSA) and hexafluoropropylene oxide dimer acid (HFPO-DA) were detected in more than 50% samples indicating the use of alternatives. Fluorotelomer carboxylic acid (FTCA) and fluorotelomer unsaturated acid (FTUCA) were found in the dust, implying the degradation of fluorotelomer alcohols (FTOH). The highest concentration of ∑PFAA (43 ng/m2) was found in outdoor dust from Xinzhou, Shanxi Province. Higher ∑PFAA concentrations were found in indoor dust than outdoor in 6 paired samples (3 from Feb. 14 and 3 from Feb. 21). In Tianjin and Handan, the concentrations of ∑PFAA from outdoor surfaces were higher in sampling campaign I (SC I, Feb. 21) than in sampling campaign II (SC II, Feb. 14), implying intensive outdoor release. The exposure of 2-year-old toddlers to PFAA via hand-to-mouth ingestion and dermal absorption was estimated; the mean values of intake were 2.1 and 1.5 pg/kg body weight, respectively, assuming an exposure time of 1 h.

Size distribution and inhalation exposure of airborne particle-bound polybrominated diphenyl ethers, new brominated flame retardants, organophosphate esters, and chlorinated paraffins at urban open consumption place.

At present, the global urban population has exceeded half of the total population and is still on the rise. Urban air pollution has attracted much attention, but most of the research focuses on typical pollution sources and indoor environment. This study reports the occurrence characteristics of particle-bound polybrominated diphenyl ethers (PBDEs), new brominated flame retardants (NBFRs), organophosphate esters (OPEs), short-chain chlorinated paraffins (SCCPs), and medium-chain chlorinated paraffins (MCCPs) at urban open consumption place. Among those pollutants detected in this study, the level of CPs was generally higher than other urban outdoor environments, and even higher than few indoor environments, such as house in Guangzhou (China) and Stockholm (Sweden). The size distributions of PBDEs and NBFRs exhibited bimodal peaks and that of SCCPs presented a unimodal peak, whereas no obvious trend was observed for OPEs or MCCPs. Additionally, the results of calculating the deposition fluxes of target pollutants in various regions based on the size distribution confirmed that total deposition was dominated by deposition in the head airways and alveolar region, and inhalation exposure in the current environment poses no significant health risk. Both discrepancy of the spatial distribution and principal component analysis indicated that sources of these organic pollutants may be related to the type of stores. Various construction and decoration materials might have been responsible for the high concentrations of OPEs and CPs, and thus, these materials require further analysis.

Insights into Persistent Toxic Substances in Protective Cases of Mobile Phones: Occurrence, Health Risks, and Implications.

Despite the popularity of smartphones worldwide, persistent toxic substances (PTSs) in protective cases of mobile phones (PCMPs) and their health risks via direct skin contact have been ignored. This study investigated PTSs in PCMPs made in China with different materials and sales territory and their potential harm to human health. Polybrominated diphenyl ethers (PBDEs, 6.40 ng/g), new brominated flame retardants (NBFRs, 144 ng/g), organophosphate esters (OPEs, 10.1 µg/g), short-chain chlorinated paraffins (SCCPs, 3.58 µg/g), medium-chain chlorinated paraffins (MCCPs, 3.17 µg/g), and heavy metals (HMs, 72.3 µg/g) were detected. It was found that the different concentrations and compositions depend on the material, region, and use. Moreover, the raw materials used to fabricate PCMPs are of variable quality and may include recycled plastic waste. There are no standard quality specifications for PCMPs, and different materials have different properties, including specific surface area and adsorption ability. The risk assessment performed by Monte Carlo simulations indicated that the PTSs evaluated pose no health risks to the general population and may have adverse effects on individual high-exposure populations. According to the results of this work, it is suggested that more stringent global specifications for the selection of raw materials should be established, including the content and structural characteristics of PTSs, limitations on the use of additives in the production process, and the handling after use.

Regional characteristics of atmospheric δ34S-SO42- over three parts of Asia monitored by quartz wool-based passive samplers.

A new method is presented for measuring atmospheric contents and δ34S-SO42- in airborne particulate matter using quartz wool disk passive air samplers (Pas-QW). The ability of Pas-QW samplers to provide time-integrated measurements of atmospheric SO42- was confirmed in a field calibration study. The average sampling rate of SO42- measured was 2.3 ± 0.3 m3/day, and this was not greatly affected by changes in meteorological parameters. The results of simultaneous sampling campaign showed that the average SO42- contents in Pakistan and the Indochina Peninsula (ICP) were relatively lower than that of China. The spatial distribution of SO42- concentrations was largely attributed to the development of the regional economies. The range of δ34S values observed in Pakistan (4.3 ± 1.4‰) and the ICP (4.5 ± 1.2‰) were relatively small, while a large range of δ34S values was observed in China (3.9 ± 2.5‰). The regional distribution of sulfur isotope compositions was significantly affected by coal combustion. A source analysis based on a Bayesian mixing model showed that 80.4 ± 13.1% and 19.6 ± 13.1% of artificial sulfur dioxide (SO2) sources in China could be attributed to coal combustion and oil combustion, respectively. The two sources differed greatly between regions, and the contribution of oil combustion in cities was higher than previously reported data obtained from emission inventories. This study confirmed that the Pas-QW is a promising tool for simultaneously monitoring atmospheric δ34S-SO42- over large regions, and that the results of the isotope models can provide a reference for the compilation of SO2 emission inventories.

Occurrence and sources of PCBs, PCNs, and HCB in the atmosphere at a regional background site in east China: Implications for combustion sources.

Multiple types of persistent organic pollutants (POPs), such as polychlorinated biphenyls (PCBs), polychlorinated naphthalenes (PCNs), and hexachlorobenzene (HCB), can be unintentionally released from combustion or thermal industrial processes, which are speculated to be the main sources of these contaminants, as they were banned on production and use since several decades ago. In this study, concentrations and sources of 40 PCBs, 39 PCNs, and HCB were analyzed in air samples collected during the period 2012-2015 at a background site in east China. ΣPCBs, ΣPCNs, and HCB were in the range of 9-341 pg/m3, 6-143 pg/m3, and 14-522 pg/m3, respectively. Seasonal characteristics with high levels in winter and low levels in summer were observed for PCNs and HCB. PCBs also exhibited slightly higher levels in winter. Source apportionment was conducted, using polycyclic aromatic hydrocarbons (PAHs) as combustion sources indicator, combined with principal component analysis (PCA) and positive matrix factorization (PMF) model. The results indicated that the legacy of past produced and used commercial PCBs was the dominant contributor (∼56%) to the selected PCBs in the atmosphere in east China. PCNs were mainly emitted from combustion sources (∼64%), whereas HCB almost entirely originated from combustion process (>90%).

Emerging and legacy per- and polyfluoroalkyl substances in water, sediment, and air of the Bohai Sea and its surrounding rivers.

Per- and polyfluoroalkyl substances (PFASs) contamination in the Bohai Sea and its surrounding rivers has attracted considerable attention in recent years. However, few studies have been conducted regarding the distribution of PFASs in multiple environmental media and their distributions between the suspended particles and dissolved phases. In this study, surface water, surface sediment, and air samples were collected at the Bohai Sea to investigate the concentration and distribution of 39 targeted PFASs. Moreover, river water samples from 35 river estuaries were collected to estimate PFAS discharge fluxes to the Bohai Sea. The results showed that total ionic compound (Σi-PFASs) concentrations ranged from 19.3 to 967 ng/L (mean 125 ± 152 ng/L) in the water and 0.70-4.13 ng/g dw (1.78 ± 0.76 ng/g) in surface sediment of the Bohai Sea, respectively. In the estuaries, Σi-PFAS concentrations were ranged from 10.5 to 13500 ng/L (882 ± 2410 ng/L). In the air, ΣPFAS (Σi-PFASs + Σn-PFASs) concentrations ranged from 199 to 678 pg/m3 (462 ± 166 pg/m3). Perfluorooctanoic acid (PFOA) was the predominant compound in the seawater, sediment, and river water; in the air, 8:2 fluorotelomer alcohol was predominant. Xiaoqing River discharged the largest Σi-PFAS flux to the Bohai Sea, which was estimated as 12,100 kg/y. Some alternatives, i.e., 6:2 fluorotelomer sulfonate acid (6:2 FTSA), hexafluoropropylene oxide dimer acid (HFPO-DA), and chlorinated 6:2 polyfluorinated ether sulfonic acid (Cl-6:2 PFESA), showed higher levels than or comparable concentrations to those of the C8 legacy PFASs in some sampling sites. The particle-derived distribution coefficient in seawater was higher than that in the river water. Using high resolution mass spectrometry, 29 nontarget emerging PFASs were found in 3 river water and 3 seawater samples. Further studies should be conducted to clarify the sources and ecotoxicological effects of these emerging PFASs in the Bohai Sea area.

Spatiotemporal variations of chlorinated paraffins in PM2.5 from Chinese cities: Implication of the shifting and upgrading of its industries.

To highlight the levels and distributions and to assess the risk of human exposure of chlorinated paraffins (CPs) in PM2.5 in China, the concentrations and homologue patterns of short-chain chlorinated paraffins (SCCPs) and medium-chain chlorinated paraffins (MCCPs) in PM2.5 from 10 cities in China were studied in 2013 and 2014. The mean concentrations of ΣSCCPs and ΣMCCPs were 19.9 ± 41.1 ng m-3 and 15.6 ± 18.6 ng m-3, respectively. Unexpectedly, the highest pollution levels occurred in two central cities (Xinxiang and Taiyuan) rather than in well-known eastern megacities such as Beijing, Nanjing, Shanghai, and Guangzhou. By comparing with earlier research, it has indicated the trend of CPs industry shifting from large eastern cities to small and medium-sized cities in central China to some extent. In addition, the composition pattern of SCCPs demonstrated an obviously differences from previous studies, with C11 and Cl7 predominating and accounting for 45.1% and 24.9%, respectively. Meanwhile, the ratio of MCCPs/SCCPs in most cities was less than 1.00 except for Guangzhou (1.92), Shanghai (1.29), and Taiyuan (1.11). Combined with the results of correlation analysis and principal component analysis, the observed pollution characteristics of CPs in PM2.5 had similar sources, which were more influenced by the ratio of MCCPs/SCCPs than by organic carbon, elemental carbon, temperature, population, and gross domestic product. Overall, the composition of CPs reflected the characteristics of local industrial production and consumption, and also implied efforts of Chinese enterprises to reduce the content of short carbon groups of CPs production. The CPs mainly deposited in head airways during the process of entering the human respiratory system. However, at the present levels, there was no significant carcinogenic effect for human health.

Polycyclic aromatic hydrocarbons in the atmosphere and soils of Dalian, China: Source, urban-rural gradient, and air-soil exchange.

We investigated the concentrations, distributions, and sources of PAHs in the air and soils of Dalian, China, as well as their air-soil exchange trends. Total concentrations of PAHs in the air ranged from 6.37 to 124 ng/m3 with an average of 23.1 ± 26.6 ng/m3, while Σ15PAHs in the soils ranged from 42.8 to 28600 ng/g with an average of 2580 ± 5730 ng/g. Significant spatial distribution of PAHs was discovered in the soils with a clear urban-suburban-rural decreasing gradient, suggesting urban area is more contaminated by PAHs due to frequent and intensive human activities. However, high PAH concentrations were also discovered in the air from several rural sites, implying some PAH sources have shifted from urban to suburban or rural areas. Source apportionment indicated that major sources of PAHs in the urban and suburban soils were traffic emission/oil spill and coal combustion respectively, whereas major sources in the rural soils were diverse. Air-soil partitioning result suggested that 3-ring PAHs were mostly volatilized from soil, 6-ring PAHs were deposited into soil, while the trends of 4∼5-ring PAHs varied with sampling site. Fluoranthene, Pyrene, and Chrysene were mostly discovered to be volatilized in the urban and suburban areas, but equilibrium or deposited in the rural area, indicating a potential urban-to-rural transport of PAHs. The atmospheric transport and source shift of PAHs from urban to rural areas highlighted the importance of PAH source control on a regional scale.

[Effects of Vehicle Emissions on Heavy Metals and Polycyclic Aromatic Hydrocarbons Pollution in Road Dust in Xinxiang].

In this study, samples were taken of the surface dust of main roads in Xinxiang City, and the concentrations of five heavy metals (Cd, Pb, Cr, Cu and Zn) and fifteen polycyclic aromatic hydrocarbons (PAHs) were determined by inductively coupled plasma mass spectrometry (ICP-MS) and gas chromatography-mass spectrometry (GC-MS), respectively. Meanwhile, the effects of vehicle emissions on the pollution characteristics were investigated. The results showed that the concentrations of heavy metals and PAHs ranged from 2.58 to 1560 mg·kg-1 and ND to 1.30 mg·kg-1, respectively. Overall, the concentrations of heavy metals and PAHs increased with a decrease in dust particle size. In terms of composition, the heavy metals were dominated by Zn while the high-molecular-weight PAHs were mainly homologous. In spatial distribution, the concentrations of heavy metals and PAHs were different. The total concentrations of heavy metals in road dust near Renmin Road, Xiaodian Industrial Park, and Cement Plant were the highest, while the high concentrations of PAHs appeared in the dust of Renmin Road, Upper Expressway, and 107 National Highway. Pearson correlation analysis showed that there was no positive correlation between the five heavy metals and fifteen PAHs. Then cluster analysis and factor analysis indicated that the PAHs were greatly affected by vehicle emissions, while the heavy metals were basically unaffected.

Polyurethane heat preservation materials: The significant sources of organophosphorus flame retardants.

The concentrations and compositions of organophosphorus flame retardants (OPFRs) in various heat preservation materials from different brands and types in China were investigated, as well as their OPFR burdens and emission amounts. The average concentrations of ΣOPFRs were 41.4 ±â€¯10.2, (7.1 ±â€¯4.0) × 104, and 56.3 ±â€¯19.3 µg/g in phenolic foams (PF), polyurethane foams (PUR), and extruded polystyrene boards (XPS), respectively. OPFRs in the PUR materials were ∼3 orders of magnitude higher than those in the other two materials, suggesting that organophosphate esters were added as flame retardants (FRs) in the PUR materials. Obvious variations in the concentrations and compositions of OPFRs were discovered in those heat preservation materials due to their material types, brands, and fire-ratings, as well as contaminations. TCIPP was the most dominant OPFR with a range from 22.3 (in PF) to 6.73 × 104 (in PUR) µg/g, which emphasized that TCIPP was the most commonly used flame retardant additives in China. Based on the OPFR concentrations, OPFR emission rates, and application amounts of heat preservation materials, we calculated the total burdens of OPFRs in those materials and their emission amounts in China. The potential total burden of OPFRs in the completed new buildings of China in 2017 was estimated to be ∼(2.37 ±â€¯1.11) × 104 t, while the total emission of OPFRs from those new materials was ∼3.19 ±â€¯1.65 t/y. As significant sources of OPFRs, the heat preservation materials used in exterior or interior walls may pose potential health risks to humans.

[Distribution and Fluxes of Perfluoroalkyl and Polyfluoroalkyl Substances in the Middle Reaches of the Yellow River (Weinan-Zhengzhou Section)].

Surface water samples were collected in the middle reaches of the Yellow River (Weinan-Zhengzhou section) and all 28 perfluoroalkyl and polyfluoroalkyl substance (PFAS) levels were measured using high-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS). The results show that the levels of PFASs in the water and particle phase are 18.4-56.9 ng·L-1 and 26.8-164 ng·g-1, respectively. Perfluorohexanoic acid (PFHxA) in the water and particle phases is the main pollutant, accounting for 27% and 16% of the total concentrations, respectively, and 3H-perfluoro-3-[(3-methoxy-propoxy)-propanoate] acid (ADONA) and chlorinated polyfluorinated ethersulfonic acids (6:2 and 8:2 Cl-PFESA) were detected in the particle phase, indicating that the use of PFAS alternatives gradually increases. The lgKd of PFASs between the water and particle phase ranges from 2.95±0.553 (PFPeA) to 3.85±0.237 (8:2 FTUCA)and the adsorption of fluorotelomer carboxylic acids (FTCAs) and fluorotelomer unsaturated carboxylic acids (FTUCAs) on particulate matter increases with increasing of carbon chain length. Perfluoroalkane sulfonic acids (PFSAs) are more easily adsorbed by particulate matter than perfluoroalkyl carboxylic acids (PFCAs). The fluxes of PFASs in the Weinan-Zhengzhou section of the Yellow River show a decrease at first and then increase, indicating that this section receives pollution inputs from the upstream and tributaries. In addition, the results show that the fluxes of PFASs in the water phase are greater than those in the particle phase.

Temporal variations and potential sources of organophosphate esters in PM2.5 in Xinxiang, North China.

We monitored the concentrations of 10 organophosphate esters (OPEs) in 52 fine particulate matter (PM2.5) samples in Xinxiang, Henan Province, North China, in 2015. During the sampling period, the OPE concentrations in most samples (n = 47) differed minimally and were relatively stable (mean: 2.02 ±â€¯0.93 ng m-3), although several samples (n = 5) had high total OPE (Æ©10OPE) concentrations (mean: 9.99 ±â€¯5.69 ng m-3), which may have been influenced by high PM2.5 levels. Meanwhile, some samples had high PM2.5 concentrations but low Æ©10OPE concentrations (i.e. low OPE/PM2.5 ratios) or low PM2.5 concentrations but high Æ©10OPE concentrations, which might have been influenced by air mass sources. Therefore, we assessed air mass sources using the Hybrid Single Particle Lagrangian Integrated Trajectory (HYSPLIT) model and wind direction frequency data, and subsequently analysed PM2.5 and OPE sources using a potential source contribution function (PSCF) model. The results revealed that air mass sources couldn't represent the source of specific pollutants, including PM2.5 and OPEs. Generally, both PM2.5 and OPEs were from Henan and Shandong Provinces; however, the major source areas differed, which may have resulted from diverse pollution characteristics in various source areas. The principal component analysis and PSCF results revealed that the 10 OPEs could be segmented into three groups, which were associated with different source areas. These results suggested that pollution characteristics of contaminants in source areas should be considered in source apportionment.

Short- and medium-chain chlorinated paraffins in the Henan section of the Yellow River: Occurrences, fates, and fluxes.

Short- and medium-chain chlorinated paraffins (SCCPs and MCCPs) were measured in sediment and suspended particulate matter (SPM) from the middle and lower reaches of the Yellow River in the three seasons to elucidate their environmental behavior. The mean concentrations of ∑SCCPs and ∑MCCPs were 262 and 97.1 ng g-1 dw (dry weight) in sediment and 17,055 and 2573 ng g-1 dw in SPM, respectively, and higher SCCP levels did not clearly reflect a shift to more MCCPs in this section of the Yellow River. The predominant homologue groups were C10-CP and C11-CP for SCCPs and C14-CP for MCCPs. The CPs possibly mainly derived from the use of CP commercial mixtures, mainly included CP-42 and CP-52. The spatial distributions and principal component analysis indicated that industrial inputs, dams, and topography played important roles in influencing the environmental behavior of CPs in both sediment and SPM. In addition, decreasing fluxes of CPs were observed in SPM from Tongguan to Aishan stations, particularly in reservoirs, which implies that CPs may have accumulated in the Henan section of the Yellow River.

[Analysis of Sources, Pollution Characteristics, and Human Exposure to Atmospheric New Halogenated Flame Retardants in Selected Areas].

Atmospheric gaseous and particle samples were collected using high-volume active samplers in Guangzhou and Wuzhishan. Concentrations of all the eight selected new halogenated flame retardants (NHFRs), including syn-DP, anti-DP, TBPH, PBEB, HBB, TBE, TBB, and DBDPE, were measured. The mean ∑NHFR concentration was significantly higher in Guangzhou (335 pg·m-3) than in Wuzhishan (90.6 pg·m-3). DBDPE was the most abundant component in Guangzhou, accounting for 66.9% of the ∑NHFR concentration, while TBPH was the major component (65.8%) in Wuzhishan. This indicates different pollution characteristics in Guangzhou and Wuzhishan. In addition, ∑NHFR concentration presented distinct seasonal variations only in Guangzhou, which could result from the different sources of origin of NHFRs. Principle component analysis showed that the atmospheric NHFRs in Guangzhou and Wuzhishan could originate from different sources. In the light of the results of wind frequency and HYSPLIT model analysis, NHFRs seem to originate mainly from the emissions from surrounding areas, including from the inputs of e-waste recycling, industrial activities, and re-volatilization of consumer goods in Guangzhou, while NHFRs mainly seem to originate from the movement of air mass over the Pearl River Delta and the seas in Wuzhishan. Meanwhile, several NHFRs presented different loading patterns in Guangzhou and Wuzhishan, and the emissions from different sources and commercial products could be the impactors. With detection of high NHFR concentrations in the atmosphere of Guangzhou, the long-time exposure of the surrounding residents (especially infants) is suspected to cause potential health risk.