Interactions of monolayer molybdenum disulfide sheets with metalloid antimony in aquatic environment: Adsorption, transformation, and joint toxicity.

The tremendous application potentiality of transitional metal dichalcogenides (TMDs), such as molybdenum disulfide (MoS2) nanosheets, will unavoidably lead to increasing release into the environment, which could influence the fate and toxicity of co-existed contaminants. The present study discovered that 59.8 % of trivalent antimony [Sb(III)] was transformed by MoS2 to pentavalent Sb [Sb(V)] in aqueous solutions under light illumination, which was due to hole oxidation on the nanosheet surfaces. A synergistic toxicity between MoS2 and Sb(III, V) to algae (Chlorella vulgaris) was observed, as demonstrated by the lower median-effect concentrations of MoS2 + Sb(III)/Sb(V) (13.1 and 20.9 mg/L, respectively) than Sb(III)/Sb(V) (38.8 and 92.5 mg/L, respectively) alone. Particularly, MoS2 at noncytotoxic doses notably increased the bioaccumulation of Sb(III, V) in algae, causing aggravated oxidative damage, photosynthetic inhibition, and structural alterations. Metabolomics indicated that oxidative stress and membrane permeabilization were primarily associated with down-regulated amino acids involved in glutathione biosynthesis and unsaturated fatty acids. MoS2 co-exposure remarkably decreased the levels of thiol antidotes (glutathione and phytochelatins) and aggravated the inhibition on energy metabolism and ATP synthesis, compromising the Sb(III, V) detoxification and efflux. Additionally, extracellular P was captured by the nanosheets, also contributing to the uptake of Sb(V). Our findings emphasized the nonignorability of TMDs even at environmental levels in affecting the ecological hazard of metalloids, providing insight into comprehensive safety assessment of TMDs.

Potential source and health risks of black carbon based on MERRA-2 reanalysis data in a typical industrial city of North China Plain.

Black carbon (BC) significantly affects climate, environmental quality, and human health. This study utilised Modern-Era Retrospective Analysis for Research and Applications, version 2 (MERRA-2), which can compensate for the shortcomings of ground BC monitoring in spatial-temporal distribution to study the pollution characteristics of BC and potential pollution sources in a typical industrial city (Xinxiang) with serious air pollution in northern China. The results showed that average daily ground observation and MERRA-2 concentration of BC of 7.33 µg m-3 and 9.52 µg m-3. The mean BC concentration derived from MERRA-2 reanalysis data was higher than ground measurement due to resolution limitations and pollution from the northern regions. The reliability of the MERRA-2 data was confirmed through correlation analysis. Consideration of the spatial distribution of BC from MERRA-2 and incorporating the potential source contribution function (PSCF), concentration-weighted trajectory (CWT), and emission inventory, other possible source areas and primary sources of BC in Xinxiang were investigated. The results indicated that implementing transportation and residential emission control measures in Henan Province and its surrounding provinces, such as Hebei Province, will effectively decrease the BC level in Xinxiang City. A passively smoked cigarettes model was used to evaluate the risk of BC exposure. The percentage of lung function decrement (PLFD) was the highest in school-age children, while the impact on lung cancer (LC) health risk was comparatively lower. Notably, the BC health risk in Xinxiang was lower than in most cities across Asia.

Quantitative characterization of resident' exposure to typical semi-volatile organic compounds (SVOCs) around a non-ferrous metal smelting plant.

To comprehensively characterize residents' exposure to major semi-volatile organic compounds (SVOCs), samples of indoor floor wipes, size-segregated airborne particles, gaseous air, food, and paired skin wipes were simultaneously collected from residential areas around a large non-ferrous metal smelting plant as compared with the control areas, and three typical SVOCs (including polychlorinated biphenyls (PCBs), polycyclic aromatic hydrocarbons (PAHs), and halogenated PAHs (HPAHs)) were determined. Comparison and correlation analysis among matrices indicated PAHs were the major contaminants emitted from metal smelting activities compared to HPAHs and PCBs, with naphthalene verified as the most important characteristic compound, and their accumulation on skin may be a comprehensive consequence of contact with floor dust and air. While patterns of human exposure pathways for the SVOCs were found to be clearly correlated to their vapor pressure, dermal absorption was the major contributor (51.1-76.3%) to total carcinogenic risk (TCR) of PAHs and HPAHs for surrounding residents, especially for low molecular weight PAHs, but dietary ingestion (98.6%) was the dominant exposure pathway to PCBs. The TCR of PAHs exceeded the acceptable level (1 × 10-4), implying smelting activities obviously elevated the health risk. This study will serve developing pertinent exposure and health risk prevention measures.

Coking-Produced Aromatic Compounds in Urine of Exposed and Nonexposed Populations: Exposure Levels, Source Identification, and Model-Based Health Implications.

Coking contamination in China is complex and poses potential health risks to humans. In this study, we collected urine samples from coking plant workers, nearby residents, and control individuals to analyze 25 coking-produced aromatic compounds (ACs), including metabolites of polycyclic aromatic hydrocarbons (PAHs) and their derivatives, chlorophenols, and nitrophenols. The median concentration of total ACs in urine of workers was 102 µg·g-1 creatinine, significantly higher than that in the other two groups. Hydroxy-PAHs and hydroxy hetero-PAHs were the dominant ACs. Workers directly exposed from coking industrial processes, i.e., coking, coal preparation, and chemical production processes, showed higher concentrations of hydroxy-PAHs and hydroxy hetero-PAHs (excluding 5-hydroxyisoquinoline), while those from indirect exposure workshops had higher levels of other ACs, indicating different sources in the coking plant. The AC mixture in workers demonstrated positive effects on DNA damage and lipid peroxidation with 5-hydroxyisoquinoline and 3-hydroxycarbazole playing a significant role using a quantile g-computation model. Monte Carlo simulation revealed that coking contamination elevated the carcinogenic risk for exposed workers by 5-fold compared to controls with pyrene, pentachlorophenol, and carbazole contributing the most, and workers from coking process are at the highest risk. This study enhances understanding of coking-produced AC levels and provides valuable insights into coking contamination control.

Nontarget Screening of Novel Urinary Biomarkers for Occupational Exposure to Toxic Chemicals from Coking Industry Using HPLC-QTOF-MS.

High-resolution mass spectrometry is an advanced technique for comprehensive screening of toxic chemicals. In this study, urine samples were collected from both an occupationally exposed population at a coking site and normal inhabitants to identify novel urinary biomarkers for occupational exposure to coking contaminants. A coking-site-appropriate analytical method was developed for unknown chemical screening. Through nontarget screening, 515 differential features were identified, and finally, 32 differential compounds were confirmed as candidates for the current study, including 13 polycyclic aromatic hydrocarbon (PAH) metabolites. Besides monohydroxy-PAHs (such as 1-&2-naphthol, 2-&9-hydroxyfluorene, 2-&4-phenanthrol, and 1-&2-hydroxypyrene), many other PAH metabolites including dihydroxy metabolites, PAH oxide, and sulfate conjugate were detected, suggesting that the quantification based solely on monohydroxy-PAHs significantly underestimated the human exposure to PAHs. Furthermore, several novel compounds were recognized that could be considered as biomarkers for the exposure to coking contaminants, including quinolin-2-ol (1.10 ± 0.44 ng/mL), naphthylmethanols (11.4 ± 5.47 ng/mL), N-hydroxy-1-aminonaphthalene (0.78 ± 0.43 ng/mL), hydroxydibenzofurans (17.4 ± 7.85 ng/mL), hydroxyanthraquinone (0.13 ± 0.053 ng/mL), and hydroxybiphenyl (2.70 ± 1.03 ng/mL). Despite their lower levels compared with hydroxy-PAHs (95.1 ± 30.8 ng/mL), their severe toxicities should not be overlooked. The study provides a nontarget screening approach to identify chemicals in human urine, which is crucial for accurately assessing the health risks of toxic chemicals in the coking industry.

Circ0005654 as a new biomarker of thyroid cancer interacting with SP1 to influence the prognosis: A case-control study.

Circular RNAs (CircRNAs) have been reported to play key roles in the progression of various cancers, including thyroid cancer (TC). Transcription factor 1 (SP1) promotes the development of thyroid cancer. This study aims at investigating the expression level of Circ0005654 in combination with Transcription factor1 (SP1) in patients with TC for diagnostic and therapeutic purposes. A total of 76 patients with thyroid cancer underwent radical surgery. Intraoperatively, thyroid cancer tissues and paired adjacent tissues and the corresponding clinicopathological data were collected. The expression of SP1 and ß-catenin in thyroid cancer and adjacent tissues was determined by immunohistochemistry (IHC) while the Circ0005654 expression level was measured by semiquantitative real-time polymerase chain reaction (sqRT-PCR). Then, we compared the variability of Circ0005654, SP1, and Wnt/ß-catenin expression in cancerous and adjacent tissues and determined the relationship between the correlation analysis and the clinicopathological features of the thyroid cancer patients. The diagnostic value of Circ0005654 in thyroid cancer tissues was analyzed with the help of the receiver operating characteristic (ROC) curve, counting the 3-year postoperative survival rate, and analyzing the effect of Circ0005654 and SP1 protein levels on the 3-year survival rate of the patients. sqRT-PCR showed that the expression level of Circ0005654 in thyroid cancer tissue was significantly higher than that of adjacent tissues. The area under the ROC of Circ0005654 was 0.9553, 95% confidence interval: (0.9211-0.9895) with a cutoff value of 0.7895, a sensitivity of 92.11%, and a specificity of 86.84%. The IHC results showed that the expression level of SP1, ß-catenin, and Wnt was higher in cancer tissues than in adjacent tissues; Circ0005654, SP1, Wnt/ß-catenin expression levels were associated with tumor diameter, lymph node metastasis, TNM stage, and envelope invasion (all P < .05). According to the Circ0005654 expression level in thyroid cancer tissue, the 3-year survival rate of the high expression group was 77.5% and 94.4% in the low expression group with a statistically significant difference; the 3-year survival rate of SP1 positive and negative patients was 78.6% and 100%, respectively, with the data being significantly different. Circ0005654 may serve as a potential biomarker for thyroid cancer diagnosis and may be involved in the development of thyroid cancer.

Distribution, sources and health risks of heavy metals in indoor dust across China.

The potential effects of heavy metals on human health have attracted increasing attention as most people spend up to 90% of their time indoors. Human exposure to heavy metals in indoor dust have only been characterised for limited regions in China, and full-scale data for different functional areas are not available. Therefore, this review analysed the concentrations, contamination characteristics, and potential health risks of seven heavy metals (including zinc (Zn), lead (Pb), copper (Cu), chromium (Cr), nickel (Ni), arsenic (As), and cadmium (Cd)) in indoor dust at 3392 sampling sites in 55 cities across 27 provincial regions of China based on literature data. Results revealed that the median heavy metal concentrations in indoor dust throughout China decreased in the following order: Zn > Pb > Cu > Cr > Ni > As > Cd. Traffic emissions and decorative materials are the primary sources of heavy metal pollution in indoor dust. No considerable non-carcinogenic risk was found for Zn, Cu, Cr, Ni, and Cd in indoor dust, while Pb and As exhibited potential non-carcinogenic risks to children, primarily distributed in cities across Southern China. Meanwhile, the carcinogenic risks posed by Cr and Ni were higher than those posed by As and Cd, especially in Southern China. Therefore, effective measures in Southern China should prioritised for controlling Pb, Cr, Ni and As pollution in indoor dust to reduce human health risk. This review is useful for policy decision-making and protecting human from exposure to heavy metals in indoor dust across China.

Amlodipine removal via peroxymonosulfate activated by carbon nanotubes/cobalt oxide (CNTs/Co3O4) in water.

Amlodipine (AML) is an effective drug that has been widely used for hypertension and angina. However, AML is frequently detected in aqueous environments, posing potential risks to human and ecological health. In this study, the degradation of AML via peroxymonosulfate (PMS) activated by CNTs/Co3O4 was investigated. CNTs/Co3O4 was prepared via a facile method, and multiple characterizations suggested that Co3O4 were uniformly dispersed on the surface of MWCNTs-COOH. Experimental results indicated that complete removal of 10 µM AML was achieved within 30 min by using 2 mg/L CNTs/Co3O4 and 4 µM PMS at 25 °C in PBS buffered solution (pH 7.0). The observed pseudo-first-order rate constant was calculated to be 0.1369 min-1. Interestingly, the presence of 100 mM Cl- resulted in a slight enhancement of AML removal rate from 0.0528 to 0.0642 min-1. The addition of 100 mM HCO3-, 5 mg/L Pony Lake fulvic acid (PLFA), or Suwannee River humic acid (SRHA) retarded AML degradation by 15.5, 0.7, and 1.6 times, respectively. As per the quenching experiments, SO4⦁- rather than ⦁OH were verified to be the dominant reactive oxygen species (ROS). Additionally, ten major intermediates were identified using TOF-LC-MS and three associated reaction pathways including ether bond broken, H-abstraction, and hydroxylation were proposed. We outlook these findings to advance the feasibility of organic contaminants removal via CNTs/Co3O4 + PMS systems that have extremely low-level PMS.

Gas-particle partition and size-segregated distribution of flame retardants in indoor and outdoor air: Reevaluation on the role of fine particles in human exposure.

In this study, we investigated the distribution of brominated and organophosphate flame retardants (BFRs and OPFRs) in the paired gaseous and nine size-segregated particulate samples collected from 8 typical indoor compartments and monthly outdoor in Xinxiang, China, respectively. For the indoor environments, total concentrations of FRs (Σ19FRs) in bulk air ranged from 3.9 ng/m3 to 37.5 ng/m3, with that in children recreation center (37.5 ng/m3) and furniture store (28.7 ng/m3) showing highest levels. In the outdoor air, Σ19FRs ranged from 3.1 ng/m3 to 13.6 ng/m3 among the 12 months, with that from late spring and summer being the highest. OPFRs had higher concentration than BFRs, with the total concentration of OPFRs accounting for 77%-99% of ∑19FRs. TCIPP (tris(chloroiso-propyl) phosphate), TCEP (tris(2-chloroethyl) phosphate), TEP (triethyl phosphate) and DBDPE (decabromodiphenyl ethane), BDE-209 (decabromodiphenyl ether) were the predominant analogs. Specifically, BFRs tended to enrich in gas phase indoors and coarse particles (aerodynamic diameters >3.3 µm) outdoors, but OPFRs mainly distributed in coarse particles both indoors and outdoors. The size distribution patterns varied among FRs, with the higher volatile FRs (e.g., TCEP, TCIPP) distributed more uniformly across particulate size. Although the distribution patterns of FRs in air were driven by multiple factors, organic carbon and element carbon in particulate matter had an influence to a certain extent. Health risks from exposure to FRs were characterized via the hazard quotient approaches. The total noncarcinogenic risks of ∑16FRs from inhalation were higher than that from air to skin transport, and the risks resulted from coarse particle-bound ∑16FRs (>3.3 µm) and gas phase were both significantly higher than that from fine fraction (<3.3 µm) in all scenarios, implying that FRs in coarse particles should not be underestimated.

Identifying dust as the dominant source of exposure to heavy metals for residents around battery factories in the Battery Industrial Capital of China.

Heavy metals (HMs) are constantly released into the environment during the production and use of batteries. Battery manufacturing has been ongoing for over six decades in the "Battery Industrial Capital" (located in Xinxiang City) of China, but the potential exposure pathways of residents in this region to HMs remain unclear. To clarify the exposure pathways and health risk of human exposure to HMs, hand wipe samples (n=82) and fingernail samples (n=36) were collected from residents (including young children (0-6 years old), children (7-12 years old) and adults (30-60 years old)) living around battery factories. The total concentrations of the target HMs (Zn, Mn, Cu, Pb, Ni, Cr, Cd, Co) in hand wipes ranged from 133 to 8040 µg/m2, and those in fingernails ranged from 9.7-566 µg/g. HM levels in the hand wipe and fingernail samples both decreased with age, and higher HM levels were observed for males than females. The HM composition profiles in these two matrices represented a high degree of similarity, with Zn as the predominant element, and thus, oral ingestion and dermal exposure via dust were expected to be the most important HM exposure pathways for residents in this region. The non-carcinogenic risks (HQs) from dermal and oral ingestion exposure to Cd, Cr, and Pb were higher than those of the other five elements for all three populations, and the HQderm of Cd for young children was 2.1 (HQoral=0.6). Moreover, the hazard index (HI) values of ∑8HMs for young children (HItotal=5.2, HIoral=2.0, HIdermal=3.2) and children (HItotal=1.6, HIoral=1.3, HIdermal=0.3) exceeded the safe threshold (1.0). Therefore, young children and children should be prioritized for protection from HM pollution, and more attention should be paid to young children's dermal exposure to Cd in this region.

Photo-Oxidative Degradation Mitigated the Developmental Toxicity of Polyamide Microplastics to Zebrafish Larvae by Modulating Macrophage-Triggered Proinflammatory Responses and Apoptosis.

Microplastics (MPs) are ubiquitous in the environment and pose substantial threats to the water ecosystem. However, the impact of natural aging of MPs on their toxicity has rarely been considered. This study found that visible light irradiation with hydrogen peroxide at environmentally relevant concentration for 90 days significantly altered the physicochemical properties and mitigated the toxicity of polyamide (PA) fragments to infantile zebrafish. The size of PA particles was reduced from ∼8.13 to ∼6.37 µm, and nanoparticles were produced with a maximum yield of 5.03%. The end amino groups were volatilized, and abundant oxygen-containing groups (e.g., hydroxyl and carboxyl) and carbon-centered free radicals were generated, improving the hydrophilicity and colloidal stability of degraded MPs. Compared with pristine PA, the depuration of degraded MPs mediated by multixenobiotics resistance was much quicker, leading to markedly lower bioaccumulation in fish and weaker inhibition on musculoskeletal development. By integrating transcriptomics and transgenic zebrafish [Tg(lyz:EGFP)] tests, differences in macrophages-triggered proinflammatory effects, apoptosis via IL-17 signaling pathway, and antioxidant damages were identified as the underlying mechanisms for the attenuated toxicity of degraded MPs. This work highlights the importance of natural degradation on the toxicity of MPs, which has great implications for risk assessment of MPs.

New equation to predict size-resolved gas-particle partitioning quotients for polybrominated diphenyl ethers.

Gas/particle (G/P) partition quotients of semi-volatile organic compounds (SVOCs) for bulk air have been widely discussed in experimental and theoretical contexts, but research on size-resolved G/P partition quotients (KPi) are scarce and limited in scope. To investigate G/P partition behavior of polybrominated diphenyl ethers (PBDEs) for size-segregated particles in the atmosphere, 396 individual size-segregated particulate samples (36 batches × 11 size-ranges), and 108 pairs of concurrent gaseous and bulk particulate samples were collected in Harbin, China. A steady-state equation based on bulk particles is derived to determine G/P partition quotients of PBDEs for size-segregated particles, which depends on the organic matter contents of size-segregated particles (fOMi). This equation can well predict KPi with knowledge of bulk partition quotient (KPS), ambient temperature, and fOMi, the results of which match well with monitoring data in Harbin and other published data collected in Shanghai and Guangzhou of China and Thessaloniki of Greece, and remedies a defect of over-estimate KPi for high-brominated PBDEs by the previous equation. In particular, the new equation contributes to obtaining the PBDEs concentrations in all atmospheric phase from partial phase, then provides a credible path to evaluate healthy exposure dose from the airborne PBDEs, by co-utilization with exposure models.

Size-distribution-based assessment of human inhalation and dermal exposure to airborne parent, oxygenated and chlorinated PAHs during a regional heavy haze episode.

The adverse health effects of haze and particle-bound contaminants in China have recently caused increasing concern, and particle size plays a significant role in affecting human exposure to haze-correlated pollutants. To this background, size-segregated particulate samples (nine size fractions (<0.4, 0.4-0.7, 0.7-1.1, 1.1-2.1, 2.1-3.3, 3.3-4.7, 4.7-5.8, 5.8-9.0 and > 9.0 µm) were collected in three scale-gradient cities in northern China and analysed for a series of parent, oxygenated and chlorinated polycyclic aromatic hydrocarbons (PAHs, O-PAHs and Cl-PAHs). The total geometric mean concentrations of PAHs and O-PAHs for Beijing, Zhengzhou and Xinxiang were 98.1 and 27.2, 77.9 and 77.5, 41.0 and 30.7 ng m-3, respectively, which were 50-200 times higher than those for Cl-PAHs (0.5, 0.7 and 0.4 ng m-3). Though unimodal size-distribution patterns were found for all these contaminants for these three cities, PAHs represented distinctly higher concentration levels around the peak fraction (0.7-2.1 µm) than O-PAHs and Cl-PAHs. With 4-6 ring PAHs as dominant components in all samples, the percentage proportion of 2-3 ring PAHs (ranging from 1% to 26%) generally increased with particle size increasing, implying the sources of these compounds varied little among the 9 size fractions in all three cities. The International Commission on Radiological Protection (ICRP) model and permeability coefficient method were synchronously applied to the size-segregated data for inhalation and dermal exposure assessment to intensively estimate the human exposure doses to airborne PAHs. Further, the incremental lifetime cancer risk (ILCR) was calculated and it's found that ILCR from inhalation was higher than that from dermal uptake for children and adults in Beijing and Zhengzhou, while the ILCR for Xinxiang presented a contrary pattern, revealing dermal uptake to be an equally significant exposure pathway to airborne PAHs compared to inhalation.

Higher health risk resulted from dermal exposure to PCBs than HFRs and the influence of haze.

To investigate the influence of haze on human dermal exposure to a series of halogenated flame retardants (HFRs) and polychlorinated biphenyls (PCBs), paired forehead wipes were collected from 46 volunteers (23 males, 23 females) using gauze pads soaked in isopropyl alcohol under heavy and light haze pollution levels. The median levels of ∑27HFRs and ∑27PCBs in all 92 samples were 672 and 1300ng/m2, respectively. Decabromodiphenyl ether (BDE-209) (171ng/m2) and decabromodiphenylethane (DBDPE) (134ng/m2) were the dominant components of HFRs, indicating that dermal exposure may also be the significant pathway for non-volatile compounds. PCB-37 contributed the most to ∑27PCBs, with a median concentration of 194ng/m2, followed by PCB-60 (141ng/m2). Generally, PBDE, PCB and DD (dehalogenated derivatives of DPs) levels on the foreheads of female participants (291, 1340, 0.92ng/m2) were higher (p=0.037, 0.001, and 0.031, respectively) than those of male participants (226, 989, and 0.45ng/m2). A significant difference (p=0.001) in PCBs was found between light (1690ng/m2) and heavy (996ng/m2) haze pollution conditions. Nevertheless, HFR levels under heavy (median=595ng/m2, ranging from 295 to 1490ng/m2) and light haze pollution conditions (ranging from 205 to 1220ng/m2 with a median of 689ng/m2) did not show significant differences (p=0.269). The non-carcinogenic health risk resulting from dermal exposure to ∑8HFRs and ∑27PCBs was 8.72×10-5 and 1.63×10-2, respectively, raising more concern about populations' exposure to PCBs than HFRs.

Spatial, seasonal and particle size dependent variations of PAH contamination in indoor dust and the corresponding human health risk.

To investigate the particle size distribution, spatial variation, and corresponding health risks of polycyclic aromatic hydrocarbons (PAHs) in indoor environments, composite settled dust samples were collected from four types of microenvironments (offices, hotels, dormitories and kindergartens) in Beijing, and each pooled dust sample was homogenized and fractionated into 9 fractions (F1 (900-2000 µm), F2 (500-900 µm), F3 (400-500 µm), F4 (300-400 µm), F5 (200-300 µm), F6 (100-200 µm), F7 (74-100 µm), F8 (50-74 µm), and F9 (<50 µm)). The total concentrations of 15 PAHs varied from 388 ng g-1 (kindergarten dust, F1) to 8140 ng g-1 (hotel dust, F7) in the 31 size-segregated samples. Particle size distribution patterns of PAHs were found to vary for the different types of dust samples. The seasonality of PAH contamination in indoor dust was discussed within 36 samples collected weekly and biweekly from two offices of one building in Beijing. Generally, the seasonal trends of PAHs in dust from these two offices were consistent, showing that PAH levels in cold seasons were higher than those in warm seasons. Diagnostic ratios and principal component analysis (PCA) indicated the important contribution of fuel combustion to PAHs in the indoor dust samples. The estimated incremental lifetime cancer risk (ILCR) values ranged from 10-6 to 10-5 for all relevant populations corresponding to the four types of microenvironments.

The non-negligible environmental risk of recycling halogenated flame retardants associated with plastic regeneration in China.

To investigate halogenated flame retardant (HFR) contents in recycled plastic materials, 23 recycled plastic samples manufactured in five Chinese provinces were randomly purchased online, and the ∑12HFR concentrations of these samples (including 8 polybrominated diphenyl ethers (PBDEs, BDE 28, 47, 99, 100, 154, 153, 183 and 209), decabromodiphenylethane (DBDPE), 1,2-bis(2,4,6-tribromophenoxy)ethane (BTBPE), and 2 dechlorane plus isomers (DP, syn-DP and anti-DP)) varied from ND to 169,000 ng g-1 (mean ±â€¯SD, 46,900 ±â€¯44,700 ng g-1). BDE 209 and DBDPE were the dominant components and their concentration ranges were from ND to 106,000 ng g-1 and ND to 81,900 ng g-1, respectively. Generally, the HFR content and plastic variety closely correlate, and the ∑HFR concentrations in the polyvinyl chloride (PVC, N = 5), polypropylene (PP, N = 9), acrylonitrile butadiene styrene (ABS, N = 5), polystyrene (PS, N = 1) and polyethylene (PE, N = 3) samples were 65,300 ±â€¯42,400, 36,700 ±â€¯56,000, 30,000 ±â€¯25,200, 24,300 and 4330 ±â€¯7500 ng g-1, respectively. The HFR abundance in plastic from Guangdong (76,000 ±â€¯56,400 ng g-1, N = 7) and Hebei (37,500 ±â€¯11,500 ng g-1, N = 4) was much higher than that for other provinces/cities.

Amplification effect of haze on human exposure to halogenated flame retardants in atmospheric particulate matter and the corresponding mechanism.

The health impact of haze is of great concern; however, few air quality studies have investigated trace pollutant contamination in the air. Size-segregated atmospheric particles (nine size fractions derived from PM10) were collected in dwelling (indoor) and traffic (outdoor) environments in Xinxiang, China, during light pollution conditions (air quality index (AQI), 60-90) and heavy pollution conditions (AQI, 350-550), and they were analysed for halogenated flame retardants (HFRs), including polybrominated diphenyl ethers (PBDEs), novel brominated flame retardants (NBFRs) and Dechlorane Plus (DP) isomers. HFR occurrence levels generally decreased in the order of PBDEs > NBFRs > DPs. The total mean abundance ratios of heavy pollution/light pollution were 4.0, 2.9, 4.4 and 3.6 for PBDEs, NBFRs, DPs and HFRs, respectively. Meteorological conditions played distinctive roles in the HFR distribution in the air. Apparent differences were found for the particle size distribution of HFRs under light and heavy pollution conditions. In general, for adults, the estimated hazard quotient (HQ) and incremental lifetime cancer risk (ILCRBDE-209) values were approximately 1.7 × 10-2 and 9.3 × 10-9 in heavy pollution conditions, respectively, which were significantly higher than those in light pollution conditions (1.8 × 10-3 and 2.1 × 10-9, respectively).

[Particle Size Distribution and Human Health Risk Assessment of Heavy Metals in Atmospheric Particles from Beijing and Xinxiang During Summer].

Under a condition of good air quality (AQI:55-90, PM10:37-97 µg·m-3, PM2.5:17-76 µg·m-3), six groups of 54 samples were collected using an Andersen cascade impactor from both the indoor and outdoor stations in Beijing and Xinxiang from June to August in 2016. The samples were digested by microwave digestion, and nine heavy metal elements (Pb, Cr, Ni, Cu, Zn, As, Cd, Mn, and Co) in the atmospheric particles were determined with an inductively coupled plasma source mass spectrometer (ICP-MS). The results showed that the enrichment index (0-3) of most elements were low in both cities except for Cd[15.0 (Beijing) and 8.47 (Xinxiang)]. Cr, Co, Cu, and Mn in the atmospheric particles from Beijing park, Cd, Pb, and Mn in the atmospheric particles from the Beijing office, Cr, Co, Ni, and As in the atmospheric particles from Xinxiang park, and all nine heavy metal elements in the atmospheric particles from roads in both cities were found to be more concentrated in the coarse fractions; however, Pb, Zn, Cd, Ni, and As in the atmospheric particles from Beijing park, Co, Zn, Ni, Cr, As, and Cu in the atmospheric particles from the Beijing office, Pb, Zn, Cd, Cu, and Mn in the atmospheric particles from Xinxiang park, and all nine metal elements in the atmospheric particles from the Beijing office showed the opposite pattern. The result of a human health risk assessment indicated that the carcinogenic risk of the five carcinogenic elements were all less than 10-4, but a lower potential cancer risk would also occur under long term exposure. For the four non-carcinogenic elements (Pb, Zn, Mn, and Cu), the non-carcinogenic health risk values of Pb, Zn, Mn, and Cu in the atmospheric particulates in Beijing were all far less than 1, which means the corresponding non-carcinogenic risk was negligible; and, except for Mn, there was no obvious non-carcinogenic risk from Pb, Zn, and Cu in the atmospheric particles of Xinxiang.

Preliminary assessment on exposure of four typical populations to potentially toxic metals by means of skin wipes under the influence of haze pollution.

To investigate the exposure risk of human beings to nine potentially toxic metals (PTMs), namely, Cu, Cr, Zn, As, Cd, Pb, Ni, Mn, and Co, skin wipe samples were collected from four types of populations, namely, children, undergraduates, security guards, and professional drivers, under different haze pollution levels in Xinxiang, China by using Ghost wipes. The Ghost wipes were quantitatively analyzed by inductively coupled plasma mass spectrometry (ICP-MS) after microwave digestion. Generally, Zn (ND-1350µg/m2 for undergraduates, ND-2660µg/m2 for security guards, ND-2460µg/m2 for children, and ND-2530µg/m2 for professional drivers) showed the highest concentration among the four populations, followed by Cu (0.02-83.4µg/m2 for undergraduates, ND-70.2µg/m2 for security guards, 23.2-487µg/m2 for children, and ND-116µg/m2 for professional drivers). As (ND-5.7µg/m2 for undergraduates, ND-2.3µg/m2 for security guards, ND-21.1µg/m2 for children, and ND-11.0µg/m2 for professional drivers) and Co (ND-6.0µg/m2 for undergraduates, ND-7.9µg/m2 for security guards, ND-13.4µg/m2 for children, and ND-2.1µg/m2 for professional drivers) showed the lowest concentrations in all populations. Remarkable differences were found among the four populations and PTM levels decreased in the following order: children, professional drivers, security guards, and undergraduates. Gender variation was discovered for undergraduates and children. Generally, PTM contamination in skin wipes collected during a light haze pollution level was generally higher than that during a heavy haze pollution level, but PTM contamination was comparable between the two haze pollution levels for children. Non-carcinogenic exposure risks to As, Cd, and Pb for all populations were higher than those for the other six elements but all of them were within the acceptable safety threshold, indicating no apparent non-carcinogenic risk.

Vehicles as outdoor BFR sources: Evidence from an investigation of BFR occurrence in road dust.

The distribution of brominated flame retardants (BFRs) including ∑8PBDEs, DBDPE, BTBPE, EH-TBB, BEH-TEBP and PBEB in road dust (RD) collected in Xinxiang, China was characterized. Analysis of RD samples indicated that the BFR abundance declined as traffic density decreased, with total mean levels of 292, 184, 163, 104 and 70 ng g-1 dust at sites from traffic intersections, main roads, collector streets, bypasses and parks, respectively. A possible explanation for this phenomenon is that the majority of BFRs may be emitted from the interior of vehicles via their ventilation systems. Of the 13 analyzed substances, BDE-209 and BEH-TEBP were the most abundant components in RD from Xinxiang. Similar amounts of ∑BDEs excluding BDE-209 were found at different types of sampling sites, and thus, atmospheric deposition is also a probable source of BFRs in RD which can be subject to air transportation. The main PBDE sources were traced to commercial products including DE-71, Bromkal 79-8DE, Saytex 201E and Bromkal 82 DE mixtures. Our results confirm that the use of deca-BDE commercial mixture is a major source of PBDE contamination in RD. Risk assessment indicated the concentrations of BFRs in RD in this study do not constitute a non-cancer or cancer risk to humans through ingestion. Annual emission fluxes of the commonly detected BFRs via RD in China were estimated to be up to 4980 kg year-1.