Characterization of VOC emissions and health risk assessment in the plastic manufacturing industry.

Volatile organic compounds (VOCs) significantly contribute to ozone pollution formation, and many VOCs are known to be harmful to human health. Plastic has become an indispensable material in various industries and daily use scenarios, yet the VOC emissions and associated health risks in the plastic manufacturing industry have received limited attention. In this study, we conducted sampling in three typical plastic manufacturing factories to analyze the emission characteristics of VOCs, ozone formation potential (OFP), and health risks for workers. Isopropanol was detected at relatively high concentrations in all three factories, with concentrations in organized emissions reaching 322.3 µg/m3, 344.8 µg/m3, and 22.6 µg/m3, respectively. Alkanes are the most emitted category of VOCs in plastic factories. However, alkenes and oxygenated volatile organic compounds (OVOCs) exhibit higher OFP. In organized emissions of different types of VOCs in the three factories, alkenes and OVOCs contributed 22.8%, 67%, and 37.8% to the OFP, respectively, highlighting the necessity of controlling them. The hazard index (HI) for all three factories was less than 1, indicating a low non-carcinogenic toxic risk; however, there is still a possibility of non-cancerous health risks in two of the factories, and a potential lifetime cancer risk in all of the three factories. For workers with job tenures exceeding 5 years, there may be potential health risks, hence wearing masks with protective capabilities is necessary. This study provides evidence for reducing VOC emissions and improving management measures to ensure the health protection of workers in the plastic manufacturing industry.

Nitrous acid in the polluted coastal atmosphere of the South China Sea: Ship emissions, budgets, and impacts.

Nitrous acid (HONO) can significantly contribute to hydroxyl radicals (OH) and thus regulate atmospheric oxidation chemistry; however, ambient HONO sources are not well quantified and vary in different environments. In this study, we conducted comprehensive field observations at a coastal site in the South China Sea and performed chemical box modelling to demonstrate contrasting budgets and impacts of diurnal atmospheric HONO derived from the sea, coastline and continent. The ship emission ratio of HONO/nitrogen oxides (NOx) (1.21 ± 0.99%) was calculated from hundreds of night-time fresh plume measurements. Offshore marine air was frequently influenced by ship exhausts, and the sea acted as an HONO sink. Heterogeneous conversions of nitrogen dioxide (NO2) on underlying surfaces and photolysis of adsorbed nitric acid (HNO3(ads)) were the major HONO sources in coastal air, when heterogeneous NO2 conversions on the ground surface and the homogeneous NO + OH reaction dominated HONO formation in continental air. HONO photolysis was a significant source of reactive radicals (ROx = OH + HO2 + RO2) in these air masses. Atmospheric box model including only homogeneous HONO source of the NO + OH reactions significantly underpredicted the OH concentration and atmospheric oxidising capacity in coastal and continental air. This study provides new insights into the complex sources and significant impacts of HONO in the polluted coastal boundary layer.

Acetaminophen degradation by hydroxyl and organic radicals in the peracetic acid-based advanced oxidation processes: Theoretical calculation and toxicity assessment.

The research on the mechanisms and kinetics of radical oxidation in peracetic acid-based advanced oxidation processes was relatively limited. In this work, HO• and organic radicals mediated reactions of acetaminophen (ACT) were investigated, and the reactivities of important organic radicals (CH3COO• and CH3COOO•) were calculated. The results showed that initiated reaction rate constants of ACT are in the order: CH3COO• (5.44 × 1010 M-1 s-1) > HO• (7.07 × 109 M-1 s-1) > CH3O• (1.57 × 107 M-1 s-1) > CH3COOO• (3.65 × 105 M-1 s-1) >> •CH3 (5.17 × 102 M-1 s-1) > CH3C•O (1.17 × 102 M-1 s-1) > CH3OO• (11.80 M-1 s-1). HO•, CH3COO• and CH3COOO• play important roles in ACT degradation. CH3COO• is another important radical in the hydroxylation of aromatic compounds in addition to HO•. Reaction rate constants of CH3COO• and aromatic compounds are 1.40 × 106 - 6.25 × 1010 M-1 s-1 with addition as the dominant pathway. CH3COOO• has high reactivity to phenolate and aniline only among the studied aromatic compounds, and it was more selective than CH3COO•. CH3COO•-mediated hydroxylation of aromatic compounds could produce their hydroxylated products with higher toxicity.

PM2.5-bound polycyclic aromatic hydrocarbons (PAHs) and nitrated-PAHs (NPAHs) emitted by gasoline vehicles: Characterization and health risk assessment.

Seventeen polycyclic aromatic hydrocarbons (PAHs) and eight nitrated PAHs (NPAHs) in PM2.5 and conventional gaseous pollutants exhausted from 54 in-use gasoline vehicles encompassing different emission standards (China 1 to China 5) were tested on the chassis and engine dynamometric test bench. With the increase of emission standards, a decrease in the emissions of PM2.5-bound PAHs and NPAHs was detected. The emission factors (EFs) of total PAHs and NPAHs in PM2.5 emitted by the vehicles with a mileage of >100,000 km were greater than that emitted by the vehicles with driving mileage of <100,000 km under all the five emission standards. The EFs of PM2.5-bound PAHs and NPAHs emitted from port fuel injection engines were larger than that from gasoline direct injection engines. The emissions of PM2.5-bound PAHs and NPAHs were less correlated with the exhaust of CO, while the hydrocarbon (HC) emissions were strongly correlated with the PM2.5-bound PAHs emissions. The emissions of NPAHs and NOx had an inverse correlation. The toxic (TEQs) of total PAHs and NPAHs in China 3, China 4 and China 5 were significantly reduced compared to China 1 and China 2, which may be related to exhaust technology improvements. Although the EFs of NPAHs were significantly lower than those of PAHs, the TEQs of NPAHs were higher, which indicates that the toxic effect of NPAHs emitted by gasoline vehicles were stronger than PAHs.

Source Contribution Analysis and Collaborative Assessment of Heavy Metals in Vegetable-Growing Soils.

Source quantification of heavy metals in farmland is essential for developing and implementing restoration strategies. We used various data analyses to identify and quantify sources of arsenic, cadmium, chromium, copper, mercury, nickel, lead, and zinc in vegetable-growing soils. A new method of collaborative assessment, combining soil environmental quality and agricultural product safety, showed that approximately 5.20% of cultivation systems were multi-contaminated by heavy metals. The nonlinear relationship between pollution sources and the comprehensive contamination situation was established, deriving from a fitted bivariate model. The model revealed that anthropogenic sources and natural origins accounted for 65.8-86.0 and 34.2-14.0% of the comprehensive pollution, respectively. These results suggested that both human activities and natural factors contributed to the decline of local soil quality and the influence of the former was more substantial than that of the latter.

Six sources mainly contributing to the haze episodes and health risk assessment of PM2.5 at Beijing suburb in 2016.

Aiming to a better understanding sources contributions and regional sources of fine particles, a total of 273 filter samples (159 of PM2.5 and 114 of PM1.0) were collected per 8 h during the winter 2016 at a southwest suburb of Beijing. Chemical compositions, including water soluble ions, organic carbon (OC), and elemental carbon (EC), as well as secondary organic carbon (SOC), were systematically analyzed and estimated. The total ions concentrations (TIC), OC, and SOC of PM2.5 were with the following order: 16:00-24:00 > 08:00-16:00 > 00:00-08:00. Since primary OC and EC were mainly attributed to the residential combustion in the night time, their valley values were observed in the daytime (08:00-16:00). However, the highest ratio value of SOC/OC was observed in the daytime. It is because that SOC is easily formed under sunshine and relatively high temperature in the daytime. Positive matrix factorization (PMF), clustering, and potential source contribution function (PSCF) were employed for apportioning sources contributions and speculating potential sources spatial distributions. The average concentrations of each species and the source contributions to each species were calculated based on the data of species concentrations with an 8 h period simulated by PMF model. Six likely sources, including secondary inorganic aerosols, coal combustion, industrial and traffic emissions, road dust, soil and construction dust, and biomass burning, were contributed to PM2.5 accounting for 29%, 21%, 17%, 16%, 9%, 8%, respectively. The results of cluster analysis indicated that most of air masses were transported from West and Northwest directions to the sampling location during the observation campaign. Several seriously polluted areas that might affect the air quality of Beijing by long-range transport were identified. Most of air masses were transported from Western and Northwestern China. According to the results of PSCF analysis, Western Shandong, Southern Hebei, Northern Henan, Western Inner Mongolia, Northern Shaanxi, and the whole Shanxi provinces should be the key areas of air pollution control in China. The exposure-response function was used to estimate the health impact associated with PM2.5 pollution. The population affected by PM2.5 during haze episodes reached 0.31 million, the premature death cases associated with PM2.5 reached 2032. These results provided important implication for making environmental policies to improve air quality in China.

Nitro and oxy-PAHs bounded in PM2.5 and PM1.0 under different weather conditions at Mount Tai in Eastern China: Sources, long-distance transport, and cancer risk assessment.

Fourteen nitro-PAHs and five oxy-PAHs associated with PM2.5 and PM1.0 were analyzed by GC-MS/MS at Mount Tai, China. 85% of the nitro-PAHs and 65% of oxy-PAHs were found in PM1.0. The combined concentration of nitro-PAHs in PM2.5 was highest in air masses associated with biomass burning (270.50pg/m3) compared with measurements from heavily polluted days (93.21pg/m3) and clean days (81.22pg/m3). A similar trend was also reflected in measurements of PM1.0. 9-FO, 9,10-ANQ, and 1-NALD were the most abundant oxy-PAHs in both PM2.5 and PM1.0 at Mount Tai. The concentration of 2+3N-FLA was markedly increased compared with other species on heavily polluted days and biomass burning days, and 9N-ANT was more concentrated in measurements from days with biomass burning emissions. Secondary generation of nitro-PAHs was also more active during periods with biomass burning. The main formation pathway of nitro-PAHs during the sampling campaign was through reactions with OH radicals, but NO3 radicals also played a significant role at night. The incremental lifetime cancer risk (ILCR) was highest during periods with biomass burning, indicating that biomass burning has a significant impact on human health. By analyzing the results of back trajectory clustering under different meteorological conditions, we determined that a large area of straw burning in the North China Plain (NCP) was the dominant source of nitro and oxy-PAHs at Mount Tai during the measurement campaign.

Trace elements in PM2.5 in Shandong Province: Source identification and health risk assessment.

The chemical compositions in PM2.5 in metropolitan areas have obtained lots of attentions, of which concerns of airborne trace elements are relatively lacking. Here, PM2.5 samples were collected simultaneously in one year at four urban sites (Zibo (ZB), Zaozhuang (ZZ), Qingdao (QD) and Jinan (JN (Shandong University)), and a rural site (JN (Miaopu)) in Shandong province. 25 elements (Al, Na, Cl, Mg, Si, S, K, Ca, Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, As, Se, Br, Sr, Cd, Ba and Pb) in PM2.5 were measured by wavelength dispersive X-ray fluorescence spectrometer (WDXRF). Most trace elements (Al, Na, Cl, Mg, Si, Ca, Ti, Mn, Fe, Co, Ni, As, Se, Br, Cd, Ba and Pb) exhibited the highest levels at ZB and the lowest at QD. Meanwhile, they presented obvious seasonal variations with the highest concentrations in winter or spring and the lowest in summer. S and K were the most abundant elements in the area. In the non-crustal trace metal elements, Zn, Pb and Mn presented the highest concentrations. Positive matrix factorization (PMF) modeling revealed that secondary formation, coal combustion and industry emissions were the main sources in the region. The health risk assessments suggested that at the five sites Cd (diet) for adults, Pb and Co for children, and Mn (diet) for both adults and children (at ZB and SDU sites) had non-carcinogenic risks. As and Pb for adults and children existed carcinogenic risks, especially Pb for children. The sources of these elements with health risks were further explored. Notably, Cd, As and Pb should be paid special attention in the area due to their high concentrations in aerosol water exceeding the acceptable health risks, especially Pb.

Heavy metal bioaccumulation and health hazard assessment for three fish species from Nansi Lake, China.

Metal accumulation in fish is a global public health concern, because the consumption of contaminated fish accounts for the primary exposure of humans to toxic metals. In this study, the concentrations of arsenic (As), cadmium (Cd), lead (Pb), and mercury (Hg) in Crucian carp (Carassius auratus),Yellow catfish (Pelteobagrus fulvidraco), and Bighead carp (Hypophthalmichthys nobilis) from Nansi Lake of China were evaluated, and compared with the corresponding historical values in 2001 when the government started to govern water environment effectively. Bioaccumulation of heavy metal was highest in P.fulvidraco, followed by C.auratus and H.nobilis. The concentrations of Pb, As, Cd were much lower than the historical values, but Hg concentration was higher, suggesting that heavy metal pollution problem in fish from Nansi Lake still exists. Health hazard assessment showed no health risk from exposure to Pb, As, Cd, and Hg by consuming fish from this lake.