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Abstract: Residential energy consumptions of both electricity and fuels are associated with emissions of many air pollutants. Temporally and spatially resolved energy consumption data are scarce in China, which are critical for a better understanding of their environmental impacts. In this study, a space-for-time substitution method was proposed and two models for predicting fuel and electricity consumptions in residential sector of China were developed using provincial data. It was found that fuel consumption was not directly proportional to heating degree day and was also affected by heating day, defined as the number of days when heating is required in a year. The models were validated against a set of historical annual data and two sets of survey data on seasonal variations. The models were applied to predict spatial and temporal variations of residential energy consumptions and emissions of various pollutants and to predict net effects of climate warming on energy consumptions and pollutant emissions. The emissions of black carbon (BC), carbon monoxide (CO), and polycyclic aromatic carbons (PAHs) in winter were significantly higher than those in other seasons. For the emissions of carbon dioxide (CO2), sulfur dioxide (SO2), and nitrogen oxides (NO x ), there were two peaks in winter and summer, with the latter increasing gradually over years. It was predicted that per-capita residential energy consumptions would reach 0.43, 0.33, and 0.26toe/cap in 2050 for IPCC scenarios of A1B, B1, and A2, respectively. Climate warming in the future would lead to less residential fuel but more electricity consumptions. Consequently, emissions of BC, CO, and PAHs would decrease mainly in cold climate zones, while emissions of CO2, SO2, and NOx would increase largely in southeast China. [Copyright &y& Elsevier]

Published emission factors (EFs) often vary significantly, leading to high uncertainties in emission estimations. There are few reliable EFs from field measurements of residential wood combustion in China. In this study, 17 wood fuels and one bamboo were combusted in a typical residential stove in rural China to measure realistic EFs of particulate matter (PM), organic carbon (OC), and elemental carbon (EC), as well as to investigate the influence of fuel properties and combustion conditions on the EFs. Measured EFs of PM, OC, and SC (EFPM, EFOC and EFEC respectively) were in the range of 0.38-6.4, 0.024-3.0, and 0.039-3.9 gJkg (dry basis), with means and standard derivation of 2.2 ± 1.2, 0.62 ± 0.64, and 0.83 ± 0.69 g/kg respectively. Shrubby biomass combustion produced higher EFs than tree woods, and both species had lower EFs than those of indoor crop residue burning (p <005). Significant correlations between EFPM, EFOC, and EFEC were expected. By using a nine-stage cascade impactor, it was shown that size distributions of PM emitted from tree biomass combustions were unimodal with peaks at a diameter less than 0.4 μm (PM0,4), much finer than the PM from indoor crop residue burning. Approximately 79.4% of the total PM from tree wood combustion was PM with a diameter less than 2.1 μm (PM2.1). PM size distributions for shrubby biomasses were slightly different from those for tree fuels. On the basis of the measured EFs, total emissions of PM, OC, and EC from residential wood combustion in rural China in 2007 were estimated at about 303, 75.7, and 92.0 Gg. [ABSTRACT FROM AUTHOR]

Abstract: Forty passive air samplers were deployed to study the occurrence of gas and particulate phase PAHs in remote, rural village and urban areas of Beijing–Tianjin region, North China for four seasons (spring, summer, fall and winter) from 2007 to 2008. The influence of emissions on the spatial distribution pattern of air PAH concentrations was addressed. In addition, the air–soil gas exchange of PAHs was studied using fugacity calculations. The median gaseous and particulate phase PAH concentrations were 222ng/m3 and 114ng/m3, respectively, with a median total PAH concentration of 349ng/m3. Higher PAH concentrations were measured in winter than in other seasons. Air PAH concentrations measured at the rural villages and urban sites in the northern mountain region were significantly lower than those measured at sites in the southern plain during all seasons. However, there was no significant difference in PAH concentrations between the rural villages and urban sites in the northern and southern areas. This urban–rural PAH distribution pattern was related to the location of PAH emission sources and the population distribution. The location of PAH emission sources explained 56%–77% of the spatial variation in ambient air PAH concentrations. The annual median air–soil gas exchange flux of PAHs was 42.2ng/m2/day from soil to air. Among the 15 PAHs measured, acenaphthylene (ACY) and acenaphthene (ACE) contributed to more than half of the total exchange flux. Furthermore, the air–soil gas exchange fluxes of PAHs at the urban sites were higher than those at the remote and rural sites. In summer, more gaseous PAHs volatilized from soil to air because of higher temperatures and increased rainfall. However, in winter, more gaseous PAHs deposited from air to soil due to higher PAH emissions and lower temperatures. The soil TOC concentration had no significant influence on the air–soil gas exchange of PAHs. [Copyright &y& Elsevier]

Abstract: Coal consumption is one important contributor to energy production, and is regarded as one of the most important sources of air pollutants that have considerable impacts on human health and climate change. Emissions of polycyclic aromatic hydrocarbons (PAHs) from coal combustion were studied in a typical stove. Emission factors (EFs) of 16 EPA priority PAHs from tested coals ranged from 6.25 ± 1.16 mg kg−1 (anthracite) to 253 ± 170 mg kg−1 (bituminous), with NAP and PHE dominated in gaseous and particulate phases, respectively. Size distributions of particulate phase PAHs from tested coals showed that they were mostly associated with particulate matter (PM) with size either between 0.7 and 2.1 μm or less than 0.4 μm (PM0.4). In the latter category, not only were more PAHs present in PM0.4, but also contained higher fractions of high molecular weight PAHs. Generally, there were more than 89% of total particulate phase PAHs associated with PM2.5. Gas-particle partitioning of freshly emitted PAHs from residential coal combustions were thought to be mainly controlled by absorption rather than adsorption, which is similar to those from other sources. Besides, the influence of fuel properties and combustion conditions was further investigated by using stepwise regression analysis, which indicated that almost 57 ± 10% of total variations in PAH EFs can be accounted for by moisture and volatile matter content of coal in residential combustion. [ABSTRACT FROM AUTHOR]