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Numerous studies have shown that graphene oxide (GO) respiratory exposure led to severe lung injury, but whether pulmonary fibrosis caused by GO respiratory exposure is related to the activation of the caspase-1/p38MAPK/TGF-β1 remains unclear. In this study, rats were administrated GO by intratracheal instillation and fed for three months, and the molecular mechanisms of GO on the pulmonary fibrosis and other organ damage caused by GO respiratory exposure were examined. The results showed that the expression of caspase-1/p38MAPK/TGF-β1 pathway-related factors were significantly elevated with the increase of exposure concentrations of GO. Those data proved that the caspase-1/p38MAPK/TGF-β1 signaling pathway was involved in the pulmonary fibrosis caused by GO respiratory exposure. The trends of related factors also proved that the caspase-1/p38MAPK/TGF-β1 pathway was likely to play a dominant role in the sub-acute and sub-chronic stages. The other organ damage examination found that the liver and spleen were damaged initially by the GO respiratory exposure. Meanwhile for the testicle, although the acute injury was severe, signs of recovery were found during the three-month trial period.

In this paper, two level III fugacity models are developed and applied using an environmental system containing six compartments, including air, aerosols, soil, water, suspended particulate matters (SPMs), and sediments, as a “unit world”. The first model, assumes equilibrium between air and aerosols and between water and SPMs. These assumptions lead to a four-fugacity model. The second model removes these two assumptions leading to a six-fugacity model. The two models, compared using four PBDE congeners, BDE-28, -99, −153, and −209, with a steady flux of gaseous congeners entering the air, lead to the following conclusions. 1. When the octanol-air partition coefficient (KOA) is less than 1011.4, the two models produce similar results; when KOA > 1011.4, and especially when KOA > 1012.5, the model results diverge significantly. 2. Chemicals are in an imposed equilibrium in the four-fugacity model, but in a steady state and not necessary an equilibrium in the six-fugacity model, between air and aerosols. 3. The results from the six-fugacity model indicate an internally consistent system with chemicals in steady state in all six compartments, whereas the four-fugacity model presents an internally inconsistent system where chemicals are in equilibrium but not a steady state between air and aerosols. 4. Chemicals are mass balanced in air and aerosols predicted by the six-fugacity model but not by the four-fugacity model. If the mass balance in air and aerosols is achieved in the four-fugacity model, the condition of equilibrium between air and aerosols will be no longer valid.

Gas/particle (G/P) partitioning is an important behavior for the atmospheric transport of polycyclic aromatic hydrocarbons (PAHs). In this study, paired daytime and nighttime air samples were collected for one year in order to study the diurnal and nocturnal variations of concentration and G/P partitioning of PAHs. Higher PAHs concentrations in total phase were observed in nighttime. The geomean (GM) concentrations of Σ

Human exposure to formaldehyde, toluene, xylene (FTX) and other volatile organic compounds (VOCs) are associated with negative health impact. To characterize the exposure and health effects of FTX and TVOC from indoor environments, we conducted an extensive monitoring campaign involving 1278 measurements of 472 indoor locations in Harbin, a megacity in China from May 2013 to March 2018. The results showed that household had the highest mean formaldehyde concentration (0.171 ± 0.084 mg m-3) among all types of indoor environments. Meanwhile, there was no significant differences in formaldehyde concentration of the living room, master bedroom, secondary bedroom and study room (p > 0.05), as well as toluene and xylene. The highest mean concentration of toluene, xylene and TVOC was measured in public bath center. Great difference was found between formaldehyde concentrations in 2013 and other years, except 2015. There were great positive nonlinear correlations between the indoor temperature and concentration of formaldehyde (p

In this study we investigated the distribution patterns, infiltration and health risk assessment of PM2.5-bound PAHs in indoor and outdoor air done in Harbin city, northeastern China. Simultaneous indoor and outdoor sampling was done to collect 264 PM2.5 samples from four sites during winter, summer, and spring. Infiltration of PAHs into indoors was estimated using Retene, Benzo [ghi]perylene and Chrysene as reference compounds, where the latter compound was suggested to be a good estimator and subsequently used for further calculation of infiltration factors (IFs). Modeling with positive matrix factorization (PMF5) and estimation of diagnostic isomeric ratios were applied for identifying sources, where coal combustion, crop residues burning and traffic being the major contributors, particularly during winter. Linear discriminant analysis (LDA) has been utilized to show the distribution patterns of individual PAH congeners. LDA showed that, the greatest seasonal variability was attributed to high molecular weight compounds (HMW PAHs). Potential health risk of PAHs exposure was assessed through relative potency factor approach (RPF). The levels of the sum of 16 US EPA priority PAHs during colder months were very high, with average values of 377 ± 228 ng m(-)(3) and 102 ± 75.8 ng m(-)(3), for the outdoors and indoors, respectively. The outdoor levels reported to be 19 times higher than the outdoor concentrations during warmer months (summer + spring), while the indoor concentrations were suggested to be 9 times and 10 times higher than that for indoor summer (average 11.73 ± 4 ng m(-3)) and indoor spring (9.5 ± 3.3 ng m(-3)). During nighttime, outdoor PAHs revealed wider range of values compared to datytime which was likely due to outdoor temperature, a weather parameter with the strongest negative influence on ∑16PAHs compared to low impact of relative humidity and wind speed.

Limited studies focus on the occurrence, removal rate and seasonal variation of substituted diphenylamine antioxidants (SDPAs) in surface water and wastewater in China. In this paper, the detection method of SDPAs was established by the ultra-performance liquid chromatography-tandem mass spectrometry. Daily variations suggested that significant variations were found for the concentrations of some SDPAs in the influent. It was found that the SDPAs could be detected in all the effluent samples and C8/C8-DPA was the predominant compound in two WWTPs. The levels of most SDPAs in the effluent were much lower than that of influent, with the removal efficiencies of total SDPAs ranged from 57.9% to 84.2%. There were significant differences with the SDPA concentrations in the influent between different seasons. Higher concentrations of SDPAs were found at downstream than those of upstream. The results of this study provide more environmental occurrence data and new insights into the research on the environmental fate of these compounds.

Arsenic levels and speciation in the total suspended particles (TSPs) were quantitatively determined by high performance liquid chromatography on-line coupled with hydride generation atomic fluorescence spectrometry in Beijing, China from February 2009 to March 2011. The high TSP levels fluctuated between 0.07 and 0.79 mg m(-3), with a mean level of 0.32 +/- 0.17 mg m(-3). The total arsenic concentrations ranged from 0.03 to 0.31 mu g m(-3) (mean: 0.13 +/- 0.06 mu g m(-3)) in Beijing's air. The concentrations of As(III) and As(V) ranged from 0.73 to 20 ng m(-3) (mean: 4.7 +/- 3.6 ng m(-3)) and from 14 to 2.5 x 10(2) ng m(-3) (mean: 67 35 ng m-3), respectively. As levels and speciation demonstrated relative higher levels in spring and autumn and lower values in summer and winter. As(V) accounted for 81-99% of the extractable species in the TSP samples which showed that As(V) was the major fraction of the extractable As. Organoarsenic species, monomethylarsonate (MMA) and dimethylarsinate (DMA) were not found in all samples. Higher values of enrichment factors demonstrated that arsenic in TSP mainly come from anthropogenic sources. High As and its species levels in air and respiratory exposure (0.30-0.84 mu g d(-1)) attributed to higher excess cancer risk ((4.2 +/- 2.0) x 10(-4)) for people in Beijing. (C) 2012 Elsevier Ltd. All rights reserved.

Understanding the seasonal variations of sources of polycyclic aromatic hydrocarbons (PAHs) in air in urban region is important to the effective control of air pollution in the region. Based on a year round dataset (from August 2008 to July 2009), the sources of atmospheric PAHs in Harbin, a typical Chinese northeastern urban city, were analyzed by principal component analysis (PCA) and positive matrix factorization (PMF). The average total (gas plus particulate) PAH concentration varied from 6.3 ng m −3 to 340 ng m −3 with a mean of 100 ± 94 ng m −3 , with higher concentrations in heating season than those in non-heating season. PCA and PMF identified similar source factors to atmospheric PAHs with obvious seasonal variation. The results obtained by PMF method indicated that the main sources were coal-fired boiler (39%), diesel engine (34%) and coal average (22%) in heating season and traffic emissions (59%), ground evaporation (18%) and coal average (17%) in non-heating season. Excellent correlation coefficients between predicted and measured concentrations of PAHs indicated that PMF was a useful model for source apportionment of PAHs in atmosphere.

Levels of dechlorane plus (DP) and "DP-like" compounds were measured in indoor dust samples collected across China. The concentrations of ΣDP and "DP-like" compounds ranged from 0.35 to 1,000 ng g(-1) and0.21 to 2.4 ng g(-1), respectively. The total DP concentration in urban sites were significantly higher than those of rural sites, while no significant difference was found for "DP-like" compounds, suggesting different sources of these compounds. Significant positive correlations were found between fsyn and latitude, and between fsyn and longitude. The deleterious risk associated with DP exposure via indoor dust for the general population in China was low and safer than expectation. For estimating human exposure via indoor dust, sensitivity analysis showed that more attention should be given to the influential variables such as the level of pollutants, body weight, and the amount of ingestion and adsorption.