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Abstract: An inventory of mercury emissions originating from waste incineration in China, including municipal solid waste, rural household waste and agricultural waste, was calculated for the period of 2004–2010. During this period, mercury emissions from waste incineration increased at an average annual rate of 3.9%, and reached 16.6 t y−1 by the end of 2010. From 2004 to 2010, the mercury emissions from rural household waste incineration accounted for 46.6% of the total waste emissions, followed by agricultural waste (30.7%) and municipal solid waste (22.7%). However, the growth rate of mercury emissions was largest for municipal solid waste incineration, with an annual rate of 37.3%, while the emissions from rural household waste showed a negative growth rate (−5.8%). The mercury emissions from waste combustion is projected to be 18.6 t y−1 by 2015, with the contribution of municipal solid waste, rural household waste and agricultural waste being 46.4%, 27.1% and 26.5%, respectively. [Copyright &y& Elsevier]

Abstract: Carbon dioxide (CO2) and carbon monoxide (CO) impact climate change and human health. The uncertainties in emissions inventories of CO2 and CO are primarily due to the large variation in measured emissions factors (EFs), especially to the lack of EFs from developing countries. China''s goals of reducing CO2 emissions require a maximum utilization of biomass fuels. Pelletized biomass fuels are well suited for the residential biomass market, providing possibilities of more automated and optimized systems with higher modified combustion efficiency (MCE) and less products from incomplete combustion. However, EFs of CO2 and CO from pellet biomass fuels are seldom reported, and a comparison to conventional uncompressed biomass fuels has never been conducted. Therefore, the objectives of this study were to experimentally determine the CO2 and CO EFs from uncompressed biomass (i.e., firewood and crop residues) and biomass pellets (i.e., pine wood pellet and corn straw pellet) under real residential applications and to compare the influences of fuel properties and combustion conditions on CO2 and CO emissions from the two types of biomass fuels. For the uncompressed biomass examples, the CO2 and CO EFs were 1649.4 ± 35.2 g kg−1 and 47.8 ± 8.9 g kg−1, respectively, for firewood and 1503.2 ± 148.5 g kg−1 and 52.0 ± 14.2 g kg−1, respectively, for crop residues. For the pellet biomass fuel examples, the CO2 and CO EFs were 1708.0 ± 3.8 g kg−1 and 4.4 ± 2.4 g kg−1, respectively, for pellet pine and 1552.1 ± 16.3 g kg−1 and 17.9 ± 10.2 g kg−1, respectively, for pellet corn. In rural China areas during 2007, firewood and crop residue burning produced 721.7 and 23.4 million tons of CO2 and CO, respectively. [Copyright &y& Elsevier]

Abstract: Due to the high costs and deployment difficulties associated with automated sampling technologies, few investigations have been published on atmospheric mercury in typical urban and rural areas in developing countries. In this study, a novel passive sampler for gaseous elemental mercury was developed and applied to characterize trends in atmospheric mercury levels across an urban–rural transect. The sampling transect originated in the city of Beijing and extended ∼150km southward into a rural region. Field deployment was conducted during September–October (autumn) and November–December (winter) in 2010. The mercury concentrations in air obtained using the passive sampler were consistent with synchronous automated measurements performed during the field deployment. The results demonstrated that atmospheric mercury concentrations increased along the urban–rural gradient in the following order in both of the two periods: urban>suburban>rural (populated)>rural (farmland). [Copyright &y& Elsevier]

Abstract: Objection: To study the pollution of atmospheric particles at winter in Beijing and compare the lung toxicity which induced by particle samples from different sampling sites. Method: We collected samples from two sampling points during the winter for toxicity testing and chemical analysis. Wistar rats were administered with particles by intratracheal instillation. After exposure, biochemically index, esimmunity indexes, histopathology and DNA damage were detected in rat pulmonary cells. Result: The elements with enrichment factors (EF) larger than 10 were As, Cd, Cu, Zn, S and Pb in the four experiment groups. The priority control of the total concentration of polycyclic aromatic hydrocarbons (PAHs) in PM10 and PM2.5 of Near-traffic source was much higher than that of Far-traffic source, it demonstrated that near the traffic source of PAHs pollution was heavier than that of Far-traffic source, as it was close to main roads Beiyuan Road, motor vehicle emissions were much higher. The pathology of lung showed that the degree of inflammation was increased with the particle diameter minished, it was the same as the detection of biochemical parameters such as lactate dehydrogenase (LDH), Total antioxidant status(T-AOC) and total protein (TP) in BALF and inflammation cytokine(interleukin-1, interleukin-6 and tumor necrosis factor-alpha) in lung homogenate. The indexes of DNA damage including the content of DNA and Olive empennage of PM2.5 were significant higher than that of PM10 at the same surveillance point (P < 0.05), near-traffic particles were higher than the far-traffic particles at the same diameter, (P < 0.05). Conclusion: Near-traffic area particles had certain pollution at winter in Beijing. Meanwhile, atmospheric particulate matters on lung toxicity were related to the particles size and distance related sites which were exposed: smaller size, more toxicity; nearer from traffic, more toxicity. [Copyright &y& Elsevier]

Abstract: Much rain and strong winds caused by a cold front occurred in Beijing during the period of Sep. 27 to Oct. 4, 2004 and led to sharp drops in maximum and mean concentrations of HONO, HCHO, O3, and NO2, i.e., the maximum concentrations were reduced by 5.9, 21.3, 45.6, and 44.4 ppb, respectively, and the mean concentrations were decreased by 4.0, 5.5, 30.3, and 32.3 ppb, respectively. For daily HO x production rates HONO photolysis was the largest contributor and over 90% contributions were from photolysis of HONO and HCHO. Large number and area percentages of soot aggregate from PM10, and high correlations between concentrations of PM10 and chemical formation of HONO suggested that heterogeneous reactions of NO2 on surfaces of soot aggregate could be a key source of HONO in the heavy traffic areas of Beijing during the night and should be considered in air quality simulations for such areas. [Copyright &y& Elsevier]

Abstract: Incorporated into the WRF–Chem model are the three HONO sources, i.e., the reaction of photo-excited NO2 with water (NO2 * chemistry), heterogeneous reactions on aerosol surfaces, and HONO emissions. Four case simulations were performed in Beijing, Tianjin, and Hebei Province (BTH region) in August of 2007. Results indicate that the NO2 * chemistry yields 30–50 ppb enhancements in daily maximum 1-h surface O3 concentrations in major cities and 3–10 ppb increases in monthly mean daily maximum 8-h surface O3 concentrations in most areas of the BTH region. Heterogeneous reactions on aerosol surfaces lead to 5–20 ppb decreases in monthly mean NOy concentrations in major cities over the BTH region. Heterogeneous reactions and HONO emissions are the largest, and the second largest contributor, accounting for ∼59% and 26% of simulated HONO concentrations, respectively. The three HONO sources produce enhancements in monthly mean daytime (10:00–17:00) concentrations of NOy (total reactive N-containing compounds), NO2, HNO3, HONO, and HOx being −1 to −5 ppb, −1 to −3 ppb, −0.3 to 0.5 ppb, 20–50 ppt, and 1–3 ppt, respectively. Comparison with observations shows that inclusion of the three HONO sources into the WRF–Chem model can considerably improve HONO and O3 simulations in the BTH region. For HONO the mean, the normal mean bias, the root mean square error, and the correlation coefficient is greatly improved from 0.04 to 0.56 ppb, from −97% to −39%, from 1.10 ppb to 0.51 ppb, and from −0.56 to 0.86, respectively, by comparison with the gas chemical mechanism only considered in the WRF–Chem model. This suggests that the three important HONO sources be included in air quality models, particularly in the areas with high emissions of NOx and particulate matter. [Copyright &y& Elsevier]

Plasma-driven photocatalysis system was prepared and performed. To overcome the treatment difficulty of volatile organic compounds, non-thermal plasma was used as a light source of photocatalysis. The removal of low-concentration toluene was investigated and secondary products were analyzed by gas chromatograph–mass spectroscopy. The plasma-driven photocatalyst reactor using direct current as a light source and titanium dioxide catalyst loaded on activated carbon fiber (TiO2/ACF) as photocatalyst was studied. It was found that plasma-driven photocatalysis system could significantly increase the removal effect of toluene. The number of secondary products was largely decreased. It means that plasma-driven photocatalysis hybrid system was an effective method for the removal of volatile organic compounds. [Copyright &y& Elsevier]