Chongguo Tian

Occurrence and spatial distribution of organophosphate ester flame retardants and plasticizers in 40 rivers draining into the Bohai Sea, north China.

Organophosphate esters (OPEs) are alternatives to polybrominated diphenyl ethers, often used as flame-retardants and plasticizers. There are few reports of OPEs in river water. This study focused on the occurrence and spatial distribution of 11 OPE congeners and one synthetic intermediate triphenylphosphine oxide (TPPO) in 40 major rivers entering into the Bohai Sea. Total OPEs ranged from 9.6 to 1549 ng L(-1), with an average of 300 ng L(-1). Tris(1-chloro-2-propyl) phosphate (TCPP) (4.6-921 ng L(-1), mean: 186 ng L(-1)) and tris(2-choroethyl) phosphate (TCEP) (1.3-268 ng L(-1), mean: 80.2 ng L(-1)) were the most abundant OPEs and their distribution patterns are similar, indicating the same source (r = 0.61, P < 0.05) and the influence of large production and consumption of chlorinated OPEs in the region. Priority should be given to TCPP, PCEP and TPPO due to their high concentrations in the rivers and potential threat to aquatic organisms.

The Use of Levoglucosan and Radiocarbon for Source Apportionment of PM2.5 Carbonaceous Aerosols at a Background Site in East China

Samples of fine particulate matter (PM2.5) were collected during July 2009 to March 2010 at a regional background site in East China. The mass concentrations of organic carbon (OC) and elemental carbon (EC) were characterized by the highest levels in winter (December to February) and the lowest abundances in summer (June to August). Conversely, the concentrations of levoglucosan were higher in summer than in winter. The observations were associated to the anthropogenic air pollutions (predominantly fossil-fuel combustions) transport from the center and north China with the northwest winds in winter and large contribution of the open biomass burning activities in South China and East China in summer, which was evident by air-mass trajectories and MODIS satellite fire counts. To assign fossil and nonfossil contributions of carbonaceous matters, the radiocarbon contents in water-insoluble OC (WINSOC) and EC in 4 combined samples representing four seasons were analyzed using the isolation system established in China. The results indicated that biomass burning and biogenic sources (59%) were the major contribution to the WINSOC, whereas fossil fuel (78%) was the dominant contributor to the refractory EC at this site. The source variation obtained by radiocarbon was consistent with other indicators, such as the OC/EC ratios and the levoglucosan concentration. Biomass burning and biogenic emissions were found to predominate in the summer and autumn, whereas fossil fuel emissions predominate in winter and spring.

Identification and quantification of shipping emissions in Bohai Rim, China

Rapid development of port and shipbuilding industry in China has badly affected the ambient air quality of coastal zone due to shipping emissions. A total of 60 ambient air samples were collected from background site of Tuoji Island in Bohai Sea strait. The air samples were analyzed for PM2.5, organic carbon (OC), element carbon (EC), inorganic elements, and water-soluble ions. The maximum concentration of PM2.5 was observed during spring (73.6 μg·m(-3)) compared to winter (39.0 μg·m(-3)) with mean of 54.6 μg·m(-3). Back trajectory air mass analysis together with temporal distribution of vanadium (V) showed that V could be the typical tracer of shipping emissions at Tuoji Island. Furthermore, the ratios of vanadium to nickel (V/Ni), vanadium to lead (V/Pb) and vanadium to zinc (V/Zn) also suggest shipping emissions at Tuoji Island. The annual average primary PM2.5 estimate of shipping emissions was 0.65 μg·m(-3) at Tuoji Island, accounting for 2.94% of the total primary PM2.5, with a maximum of 3.16% in summer and a minimum of 2.39% in autumn.

Screening of Atmospheric Short- and Medium-Chain Chlorinated Paraffins in India and Pakistan using Polyurethane Foam Based Passive Air Sampler

Production and use of chlorinated paraffins (CPs) have been increasing in India. Distribution of CPs in the area and vicinity have become a great concern due to their persistency and toxicity. Polyurethane foam based passive air samplers (PUF-PAS) was deployed in order to screen the presence of short- and medium- chain chlorinated paraffins (SCCPs and MCCPs) in the outdoor atmosphere at many sites in India (in winter 2006) and Pakistan (in winter 2011). Concentrations of SCCPs and MCCPs ranged from not detected (ND) to 47.4 and 0 to 38.2 ng m(-3) with means of 8.11 and 4.83 ng m(-3), respectively. Indian concentrations showed higher average levels of both SCCPs and MCCPs India (10.2 ng m(-3) and 3.62 ng m(-3)than the samples from Pakistan (5.13 ng m(-3) and 4.21 ng m(-3)). Relative abundance patterns of carbon number are C10 > C11 > C12 ∼ C13 for SCCPs and C14 > C15 > C16 C17 for MCCP with similarity to the profiles of samples from China, the biggest CPs producer in the world. Principal Component Analysis suggested that detected SCCPs and MCCPs in this study originated from the same emission source.

Impact of agricultural waste burning in the Shandong Peninsula on carbonaceous aerosols in the Bohai Rim, China.

A total of 11 5PM2.5 samples were collected for analyzing organic carbon (OC) and elemental carbon (EC) at Tuoji Island (TI), China from November 2011 to December 2012. The results showed that annual arithmetical means of OC and EC concentrations were 3.8 ± 2.7 and 2.2 ± 2.2 μg m(-3), which contributed 8% and 4% of PM2.5 mass concentrations, respectively. High EC concentrations occurred in winter, contributed mainly by EC outflow from the northwest source region, while high OC concentrations were found during spring, attributed largely to biofuel burning in the Shandong Peninsula, and short distance and favorable transport from the peninsula to the TI. Agricultural waste open burning in the peninsula caused the largest variability of OC concentration in summer. Eliminating agricultural field burning in the peninsula can reduce at least one-third of concentration levels and half of northward transport fluxes of OC and EC in Bohai Rim in summer.

Chemical composition of PM2.5 from two tunnels with different vehicular fleet characteristics.

The chemical compositions of PM2.5 including OC, EC, water soluble ions, elements, and organic components such as polycyclic aromatic hydrocarbons (PAHs), hopanes, and steranes, emitted in Wuzushan (WZS) and Kuixinglou (KXL) tunnels were determined. WZS tunnel is a major route for diesel vehicles traveling, while KXL tunnel has limited to diesel vehicles. The results showed that the proportions of the different constituents of PM2.5 in the Wuzushan (WZS) tunnel were OC (27.7%), EC (32.1%), elements (13.9%), and water soluble ions (9.2%). Whereas the chemical profile of PM2.5 in the Kuixinglou (KXL) tunnel was OC (17.7%), EC (10.4%), elements (8.90%), and water soluble ions (8.87%). The emission factors (EFs) of PM2.5 and proportions of SO4(2-) and Pb were decreased by vehicle emission standards and fuel quality policy in China, and the higher molecular weight PAHs (4+5+6 rings) were more abundant than the lower molecular weight PAHs (2+3 rings) in the two tunnels. The proportions of 17A(H)-21B(H)-30-Norhopane and 17A(H)-21B(H)-Hopane in the hopane and sterane were not dependent on the vehicles types. In addition, specific composition profiles for PM2.5 from gasoline-fueled vehicles (GV) and diesel-fueled vehicles (DV) emissions were drafted, which indicated that OC (0.974mg·veh(-1)·km(-1)) was the most abundant component in PM2.5, followed by Fe, Cl(-), and Mg for GV. The relative proportions of the different constituents in the PM2.5 for DV were EC (35.9%), OC (27.2%), elements (12.8%), and water soluble ions (11.7%). Both the PM2.5 EFs and EC proportions in DV were higher than those in GV, and the HMW PAHs were the dominant PAHs for both GV and DV. The PM2.5 emissions from the vehicles in Yantai were 581±513tons to 1353±1197tons for GV, and 19,627±2477tons to 23,042±2887tons for DV, respectively.

Radiocarbon-based impact assessment of open biomass burning on regional carbonaceous aerosols in North China

Samples of total suspended particulates (TSPs) and fine particulate matter (PM2.5) were collected from 29th May to 1st July, 2013 at a regional background site in Bohai Rim, North China. Mass concentrations of particulate matter and carbonaceous species showed a total of 50% and 97% of the measured TSP and PM2.5 levels exceeded the first grade national standard of China, respectively. Daily concentrations of organic carbon (OC) and elemental carbon (EC) were detected 7.3 and 2.5 μg m(-3) in TSP and 5.2 and 2.0 μg m(-3) in PM2.5, which accounted 5.8% and 2.0% of TSP while 5.6% and 2.2% for PM2.5, respectively. The concentrations of OC, EC, TSP and PM2.5 were observed higher in the day time than those in the night time. The observations were associated with the emission variations from anthropogenic activities. Two merged samples representing from south and north source areas were selected for radiocarbon analysis. The radiocarbon measurements showed 74% of water-insoluble OC (WINSOC) and 59% of EC in PM2.5 derived from biomass burning and biogenic sources when the air masses were from south region, and 63% and 48% for the air masses from north, respectively. Combined with backward trajectories and daily burned area, open burning of agricultural wastes was found to be predominating, which was confirmed by the potential source contribution function (PSCF).

Flux and budget of BC in the continental shelf seas adjacent to Chinese high BC emission source regions

This study conducted the first comprehensive investigation of sedimentary black carbon (BC) concentration, flux, and budget in the continental shelves of Bohai Sea (BS) and Yellow Sea (YS), based on measurements of BC in 191 surface sediments, 36 riverine water, and 2 seawater samples, as well as the reported data set of the atmospheric samples from seven coastal cities in the Bohai Rim. BC concentrations in these matrices were measured using the method of thermal/optical reflectance. The spatial distribution of the BC concentration in surface sediments was largely influenced by the regional hydrodynamic conditions, with high values mainly occurring in the central mud areas where fine-grained particles (median diameters>6 (i.e., <0.0156mm)) were deposited. The BC burial flux in the BS and YS ranged from 4 to 1100 mu g/cm(2)yr, and averaged 166200 mu g/cm(2)yr, which was within the range of burial fluxes reported in other continental shelf regimes. The area-integrated sedimentary BC sink flux in the entire BS and YS was 325Gg/yr, and the BS alone contributed 50% (157Gg/yr). The BC budget calculated in the BS showed that atmospheric deposition, riverine discharge, and import from the Northern Yellow Sea (NYS) each contributed 51%, 47%, and 2%. Therefore, atmospheric deposition and riverine discharge dominated the total BC influx (98%). Sequestration to bottom sediments was the major BC output pattern, accounting for 88% of the input BC. Water exchange between the BS and the NYS was also an important BC transport route, with net BC transport from the BS to the NYS.

Increase in polycyclic aromatic hydrocarbon (PAH) emissions due to briquetting: A challenge to the coal briquetting policy

Both China and UNEP recommend replacing raw coal chunks with coal briquettes in household sector as clean coal technology (CCT), which has been confirmed by the decreased emissions of particulate matter and black carbon. However, the clean effect has never been systematically checked by other pollutants like polycyclic aromatic hydrocarbons (PAHs). In this study, 5 coals with different geological maturities were processed as both chunks and briquettes and burned in 3 typical coal stoves for the measurement of emission factors (EFs) of particle-bound PAHs. It was found that the EFs of 16 parent PAHs, 26 nitrated PAHs, 6 oxygenated PAHs, and 8 alkylated PAHs for coal briquettes were 6.90 ± 7.89, 0.04 ± 0.03, 0.65 ± 0.40, and 72.78 ± 18.23 mg/kg, respectively, which were approximately 3.1, 3.7, 1.9, and 171 times those for coal chunks, respectively. Such significant increases in PAH emissions increased human health risk and challenged the policy of CCT.

Atmospheric polychlorinated naphthalenes (PCNs) in India and Pakistan

Polychlorinated naphthalenes (PCNs) are now under review by the Stockholm Convention as candidates for persistent organic pollutants (POPs) due to their persistence, toxicity, bioaccumulation, and long-range atmospheric transport. Data on PCN levels are sparse in South Asia. Atmospheric PCNs in India and Pakistan were monitored during the winter by polyurethane foam disk passive air samplers (PUF-PAS). The average concentrations were 29 pg/m(3) and 7.7 pg/m(3) in the Indian and Pakistani samples, respectively. Those concentration levels were relatively lower than the previously reported values in other Asian countries, but still considerably higher than in other sites in the world. Tri-CNs and tetra-CNs were the dominant homologues in the air, especially in India. Spatially, the PCNs were ubiquitous in the target areas, and local distribution was generally impacted by the proximity to potential sources. Major sources of PCNs in this study were the re-emission of Halowax and industrial thermal processes. Biomass burning influenced some sites in Pakistan. However, the enrichment of tri-CNs in Indian cities cannot be ascribed to either the signature of a specific source or the preferential volatilization and/or photodegradation in tropical areas. Despite this unclear issue in South Asia, the present study indicates that the potential health impact was generally comparable to that in non-urban sites worldwide.