Barbecuing or charcoal-grilling has become part of popular outdoor recreational activities nowadays; however, potential human health hazards through outdoor exposure to barbecue fumes have yet to be adequately quantified. To fill this knowledge gap, atmospheric size-fractioned particle and gaseous samples were collected near an outdoor barbecuing vendor stall (along with charcoal-grilled food items) in Xinjiang of Northwest China with a 10-stage micro-orifice uniform deposit impactor and a polyurethane foam (PUP) sampler and were analyzed for particulate matter and polycyclic aromatic hydrocarbons (PAHs). Exposure to PAHs through inhalation and dermal contact by adult consumers who spent 1 h per day near a charcoal-grilling vendor for a normal meal (lunch or dinner) amounted to a BaP equivalent (BaPeq) dosage of 3.0-77 ng day(-1) (inhalation: 2.8-27 ng day(-1) of BaPeq; dermal contact: 0.2-50 ng day(-1) of BaPeq), comparable to those (22-220 ng day(-1) of BaPeq) from consumer exposure through the consumption of charcoal-grilled meat, assumed to be at the upper limit of 50-150 g. In addition, the potential health risk was in the range of 3.1 X 10(-10) to 1.4 X 10(-4) for people of different age groups with inhalation and dermal contact exposure to PAHs once a day, with a 95% confidence interval (7.2 X 10(-9) to 1.2 X 10(-6)) comparable to the lower limit of the potential cancer risk range (1 X 10(-6) to 1 X 10(-4)). Sensitivity analyses indicated that the area of dermal contact with gaseous contaminants is a critical parameter for risk assessment. These results indicated that outdoor exposure to barbecue fumes (particularly dermal contact) may have become a significant but largely neglected source of health hazards to the general population and should be well-recognized.
The stress and the debonding of the interface in coating layers structure due to thermal loading are investigated by using boundary element methods(BEM). The nearly-singular integrals that arise in the boundary integral equation(BIE) for such thin layered structures cannot be accurately evaluated us...
PCN bacteria capable of heterotrophic-aerobic nitrogen removal was successfully applied for bioaugmented treatment of municipal wastewater in a pilot-scale SBR. At an appropriate COD/N ratio of 8, the bioaugmentation system exhibited stable and excellent carbon and nutrients removal, the averaged effluent concentrations of COD, NH4+-N, TN and TP were 20.6, 0.69, 14.1 and 0.40 mg/L, respectively, which could meet the first class requirement of the National Municipal Wastewater Discharge Standards of China (COD < 50 mg/L, TN < 15 mg/L, TP < 0.5 mg/L). Clone library and real-time PCR analysis revealed that the introduced bacteria greatly improved the structure of original microbial community and facilitated their aerobic nutrients removal capacities. The proposed emerging technology was shown to be an alternative technology to establish new wastewater treatment systems and upgrade or retrofit conventional systems from secondary-level to tertiary-level. (C) 2015 Elsevier Ltd. All rights reserved.
Broadband continuous frequency tuning (CFT) in a terahertz gyrotron is promising for advanced terahertz applications. However, it is challenging to realize broadband CFT in a conventional open cavity, because a long cavity is helpful to expand the bandwidth but is generally difficult to suppress the high Q -factor gyromonotron competition. In this paper, a tapered cavity with a long effective interaction length is proposed to expand the CFT bandwidth. The tapered circuit can reduce the Q-factor of the first-order axial mode and accordingly suppress the gyromonotron competition. By selecting a reasonable Q-factor cavity, a gyrotron could generate effective radiation sequentially under gyromonotron and gyrobackward-wave oscillator (BWO) states during the magnetic field tuning. In gyromonotron range, the bandwidth is expanded because of the cutoff frequency shifting. On the other hand, in gyro-BWO range, the bandwidth is expanded because of the axial mode transition. The CFT bandwidth of 4 GHz is realized in a tapered 330-GHz TE12,4 mode low-voltage gyrotron. The principle is important for developing broadband CFT terahertz gyrotrons.
The relativistic electron cyclotron maser (ECM) has been successfully applied to generating high-power THz wave. In order to realize the additional advantages of broadband tuning and high efficiency interaction, this paper is devoted to exploring the THz pre-bunched ECM. Other than a conventional open-cavity tunable gyrotron consecutively switching between axial modes to realize frequency tuning, a pre-bunched ECM system operates on the backward traveling-wave resonance to achieve broadband smooth tuning. Especially, an interaction circuit of specified axial profile of beam-wave detuning frequency is built to achieve high efficiency. An optimized 0.1 THz pre-bunched ECM system using an electron beam of 30 kV voltage and 3 A current is predicted to generate broad bandwidth of 10 GHz and efficiency between 10% ~ 25%. The broadband tuning pre-bunched ECM is promising for a new generation of broadband and high-power THz source.
Fifteen different types of PM2.5 mass concentration samplers were used by seven different monitoring networks at 47 locations in the Pittsburgh, Pennsylvania, region from 1999 to 2008. The samplers included Federal Reference Method (FRM) samplers, speciation samplers, tapered element oscillating microbalance (TEOM) samplers, and others. The different measurement principles used in these designs tended to lead to systematic differences (biases) when measuring the same quantity, and to differences in the typical size of random errors (imprecision) introduced by each type of sampler. Bias can take different forms either as a constant bias or as a non-constant (scale) bias, which depends on the size of the quantity being measured. The objective of the work presented here was to simultaneously calibrate the measurements made by these different samplers to remove relative biases (both constant and non-constant) so that all of the available PM2.5 data could be used interchangeably to develop exposure estimates for a retrospective epidemiology study. In order to accomplish this, we used linked temperature-stratified structural equation models, nonlinear regression models, and nonlinear mixed effects models. Applying these methods we constructed a comprehensive measurement error model that included both systematic error and random error components, and derived calibration equations that can be applied to place all of the PM2.5 mass concentration measurements on the same scale. The FRM sampler was used as the reference scale although the parameter estimates are invariant to this choice. Results showed that: (1) 50 degrees C TEOM samplers tended to show a large downward bias relative to the FRM sampler at low temperatures, and the magnitude of this bias decreased according to a nonlinear (sigmoidal) pattern with increasing temperature, (2) speciation samplers and other integrated samplers generally showed smaller biases relative to the FRM sampler that were not temperature-dependent, and (3) FRM samplers tended to be more precise than non-FRM samplers. These results are consistent with our previous work focusing on just a single monitoring site. Results are also presented here for several types of samplers that were not part of our previous study, including 30 degrees C TEOM, FDMS TEOM, and beta attenuation monitors. (C) 2015 Elsevier Ltd. All rights reserved.
The full models are estimated by spatial econometric models using county-level data from 1513 Chinese counties. The results indicate the existence of spatial contagion effects among local governments with respect to spending on local education. Financial shortages in education tend to be contagious; they affect counties or regions in geographic proximity. Contagion occurs due to three different fundamental causes: Intergovernmental competition, political economy and neighborhood watch. The possibility of contagion depends strongly on education investment, financial and economic conditions, cultural diversity, urban/rural distribution, and population structure. Poor counties are much more likely to become “infected” by neighboring financial behavior in education. The empirical evidence suggests that the speed of contagion is faster in economically underdeveloped areas than in economically developed areas.
Chengdu is an inland megacity in the Sichuan Basin, where dust influence remained an open question. During a one-year haze campaign, two dust events were identified in March 2013, indicating that desert dust can be transported to Chengdu and impacted local air quality strongly. The suggested low SO2/PM10, NO2/PM10 and PM2.5/PM10 ratios of 0.15, 0.27 and 0.40 could be used as immediate indicators for dust days. On typical dust day of March 12, PM10 was as high as 359.1 μg m−3, and crustal matter contributed 80.5% to total PM2.5 mass (106.6 μg m−3). Enrichment factors of most elements have decreased due to the dilution effect except for Ca and Mg. The dust was mainly from western and northern dust regions in China, including the “Northerly Mongolia Path”, “Western Desert Path” and “Northwestern Desert Path”. Due to the obstruction of Qinghai-Tibet Plateau on the west, the dust air to Chengdu was mostly from the northeastward direction after passing over Qinling Mountain. Moreover, the air experienced obvious elevation from its source regions driven by the cold front synoptic pattern. The spatial distribution of high AOD (Aerosol Optical Depth) values over 1.2 but low Ångström exponent of 0.5–0.6 around Chengdu verified the coarse pollution patterns. However, the dust pollution was not serious in nearby Chongqing and Guizhou and exhibited weak regional feature, a result different from those in Beijing and Shanghai.
To better understand the chemical speciation of volatile organic compounds (VOCs) and their role in ground-level ozone formation in the Beijing-Tianjin-Hebei region, China, measurements of 56 non-methane hydrocarbons (NMHCs) and 12 carbonyls were conducted at three sites in summer. Alkanes were the largest group of NMHCs (>50%), followed by alkenes and aromatics. Acetone was the most abundant carbonyl species (>50%). The OH loss rates (LOH) of VOCs were calculated to estimate their chemical reactivities. Alkenes played a predominant role in VOC reactivity, among which ethene and propene were the largest contributors. Isoprene contributed 11.61–38.00% of the total reactivity of measured VOCs. Alkenes and aromatics were the largest contributors (47.65–61.53% totally) to the total Ozone Formation Potential (OFP) of measured VOCs based on the observed mixing ratio. Isoprene was the most reactive species, but originated mainly from biogenic emissions. Ethene, m/p-xylene, toluene, propene, o-xylene, and 1-butene were considered to play significant roles in ground-level ozone formation in this region. The OFPs of total measured NMHCs increased by 10.20–22.05% when they were calculated based on the initial mixing ratio. Photochemical losses of hydrocarbons and the secondary formation of carbonyls in this region were also determined. Vehicle exhaust emissions contributed substantially to ambient VOCs.
Substantial amounts of secondary organic aerosol (SOA) can be formed from isoprene epoxydiols (IEPOX), which are oxidation products of isoprene mainly under low-NO conditions. Total IEPOX-SOA, which may include SOA formed from other parallel isoprene oxidation pathways, was quantified by applying positive matrix factorization (PMF) to aerosol mass spectrometer (AMS) measurements. The IEPOX-SOA fractions of organic aerosol (OA) in multiple field studies across several continents are summarized here and show consistent patterns with the concentration of gas-phase IEPOX simulated by the GEOS-Chem chemical transport model. During the Southern Oxidant and Aerosol Study (SOAS), 78% of PMF-resolved IEPOX-SOA is accounted by the measured IEPOX-SOA molecular tracers (2-methyltetrols, C5-Triols, and IEPOX-derived organosulfate and its dimers), making it the highest level of molecular identification of an ambient SOA component to our knowledge. An enhanced signal at C5H6O+ (m/z 82) is found in PMF-resolved IEPOX-SOA spectra. To investigate the suitability of this ion as a tracer for IEPOX-SOA, we examine fC(5)H(6)O (fC(5)H(6)O = C5H6O+ / OA) across multiple field, chamber, and source data sets. A background of similar to 1.7 +/- 0.1 parts per thousand (parts per thousand = parts per thousand) is observed in studies strongly influenced by urban, biomass-burning, and other anthropogenic primary organic aerosol (POA). Higher background values of 3.1 +/- 0.6 parts per thousand are found in studies strongly influenced by monoterpene emissions. The average laboratory monoterpene SOA value (5.5 +/- 2.0 parts per thousand) is 4 times lower than the average for IEPOX-SOA (22 +/- 7 parts per thousand), which leaves some room to separate both contributions to OA. Locations strongly influenced by isoprene emissions under low-NO levels had higher fC(5)H(6)O (similar to 6.5 +/- 2.2 parts per thousand on average) than other sites, consistent with the expected IEPOX- SOA formation in those studies. fC(5)H(6)O in IEPOX- SOA is always elevated (12-40 parts per thousand) but varies substantially between locations, which is shown to reflect large variations in its detailed molecular composition. The low fC(5)H(6)O (< 3 parts per thousand) reported in non-IEPOX-derived isoprene-SOA from chamber studies indicates that this tracer ion is specifically enhanced from IEPOX- SOA, and is not a tracer for all SOA from isoprene. We introduce a graphical diagnostic to study the presence and aging of IEPOX- SOA as a triangle plot of f(CO2) vs. fC(5)H(6)O. Finally, we develop a simplified method to estimate ambient IEPOX- SOA mass concentrations, which is shown to perform well compared to the full PMF method. The uncertainty of the tracer method is up to a factor of similar to 2, if the fC(5)H(6)O of the local IEPOX- SOA is not available. When only unit mass-resolution data are available, as with the aerosol chemical speciation monitor (ACSM), all methods may perform less well because of increased interferences from other ions at m/z 82. This study clarifies the strengths and limitations of the different AMS methods for detection of IEPOX- SOA and will enable improved characterization of this OA component.
Ambient volatile organic compounds (VOCs) were measured using an online system, gas chromatography–mass spectrometry/flame ionization detector (GC-MS/FID), in Beijing, China, before, during, and after Asia-Pacific Economic Cooperation (APEC) China 2014, when stringent air quality control measures were implemented. Positive matrix factorization (PMF) was applied to identify the major VOC contributing sources and their temporal variations. The secondary organic aerosols potential (SOAP) approach was used to estimate variations of precursor source contributions to SOA formation. The average VOC mixing ratios during the three periods were 86.17, 48.28, and 72.97 ppbv, respectively. The mixing ratios of total VOC during the control period were reduced by 44 %, and the mixing ratios of acetonitrile, halocarbons, oxygenated VOCs (OVOCs), aromatics, acetylene, alkanes, and alkenes decreased by approximately 65, 62, 54, 53, 37, 36, and 23 %, respectively. The mixing ratios of all measured VOC species decreased during control, and the most affected species were chlorinated VOCs (chloroethane, 1,1-dichloroethylene, chlorobenzene). PMF analysis indicated eight major sources of ambient VOCs, and emissions from target control sources were clearly reduced during the control period. Compared with the values before control, contributions of vehicular exhaust were most reduced, followed by industrial manufacturing and solvent utilization. Reductions of these three sources were responsible for 50, 26, and 16 % of the reductions in ambient VOCs. Contributions of evaporated or liquid gasoline and industrial chemical feedstock were slightly reduced, and contributions of secondary and long-lived species were relatively stable. Due to central heating, emissions from fuel combustion kept on increasing during the whole campaign; because of weak control of liquid petroleum gas (LPG), the highest emissions of LPG occurred in the control period. Vehicle-related sources were the most important precursor sources likely responsible for the reduction in SOA formation during this campaign.
We present mass spectrometry measurements of black carbon-containing particles made on board the R/V Atlantis during the CalNex (California Research at the Nexus of Air Quality and Climate Change) 2010 study using an Aerodyne Research Inc. soot particle aerosol mass spectrometer (SP-AMS). The R/V Atlantis was deployed to characterize air masses moving offshore the California coast and to assess emissions from sources in urban ports. This work presents a first detailed analysis of the size-resolved chemical composition of refractory black carbon (rBC) and of the associated coating species (NR-PMBC). A colocated standard high-resolution aerosol mass spectrometer (HR-AMS) measured the total nonrefractory submicron aerosol (NR-PM1). Our results indicate that, on average, 35% of the measured NR-PM1 mass (87% of the primary and 28% of the secondary NR-PM1, as obtained from the mass-weighted average of the NR-PMBC species) was associated with rBC. The peak in the average size distribution of the rBC-containing particles measured by the SP-AMS in vacuum aerodynamic diameter (d(va)) varied from 100 nm to 450 nm d(va), with most of the rBC mass below 200 d(va). The NR-PMBC below 200 nm d(va) was primarily organic, whereas inorganics were generally found on larger rBC-containing particles. Positive matrix factorization analyses of both SP-AMS and HR-AMS data identified organic aerosol factors that were correlated in time but had different fragmentation patterns due to the different instruments vaporization techniques. Finally, we provide an overview of the volatility properties of NR-PMBC and report the presence of refractory oxygen species in some of the air masses encountered.
