China is one of the regions with highest PM concentration in the world. In this study, we review the spatio-temporal distribution of PM mass concentration and components in China and the effect of control measures on PM concentrations. Annual averaged PM concentrations in Central-Eastern China reached over 100μgm, in some regions even over 150μgm. In 2013, only 4.1% of the cities attained the annual average standard of 35μgm. Aitken mode particles tend to dominate the total particle number concentration. Depending on the location and time of the year, new particle formation (NPF) has been observed to take place between about 10 and 60% of the days. In most locations, NPF was less frequent at high PM mass loadings. The secondary inorganic particles (i.e., sulfate, nitrate and ammonium) ranked the highest fraction among the PM species, followed by organic matters (OM), crustal species and element carbon (EC), which accounted for 6-50%, 15-51%, 5-41% and 2-12% of PM, respectively. In response to serious particulate matter pollution, China has taken aggressive steps to improve air quality in the last decade. As a result, the national emissions of primary PM, sulfur dioxide (SO), and nitrogen oxides (NO) have been decreasing since 2005, 2006, and 2011, respectively. The emission control policies implemented in the last decade could result in noticeable reduction in PM concentrations, contributing to the decreasing PM trends observed in Beijing, Shanghai, and Guangzhou. However, the control policies issued before 2010 are insufficient to improve PM air quality notably in future. An optimal mix of energy-saving and end-of-pipe control measures should be implemented, more ambitious control policies for NMVOC and NH should be enforced, and special control measures in winter should be applied. 40-70% emissions should be cut off to attain PM standard.

The recycling of electrical and electronic waste (e-waste) in developing countries has attracted much attention as a significant source of brominated flame retardants (BFRs). Gaseous and particle-bound BFRs were measured in the atmosphere at e-waste and rural sites in southern China during 2007–2008. The annual average concentrations in the air were 3260 ± 3370 and 219 ± 192 pg/m3 for polybrominated diphenyl ethers (PBDEs) and were 546 ± 547 and 165 ± 144 pg/m3 for non-PBDE BFRs at the e-waste and rural sites, respectively. PBDEs had unusually high relative concentrations of di- and tribrominated congeners at the e-waste site. The Clausius–Clapeyron (CC) plots showed that the gaseous concentrations of less brominated BFRs (di- through hexa-BFRs) were strongly controlled by temperature-driven evaporation from contaminated surfaces (e.g., e-waste, soils, and recycled e-waste remains) except for winter. However, weak temperature dependence at the rural site suggests that regional or long-range atmospheric transport was largely responsible for the air concentrations. Gas-particle partitioning (K P) of PBDEs correlated well with the subcooled liquid vapor pressure (P L o) for most sampling events. The varied slopes of log K P versus log P L o plots for the e-waste site (−0.59 to −1.29) indicated an influence of ambient temperature and atmospheric particle properties on the partitioning behavior of BFRs. The flat slopes (−0.23 to −0.80) for the rural site implied an absorption-dominant partitioning. This paper suggests that e-waste recycling in Asian low-latitude regions is a significant source of less brominated BFRs and has important implications for their global transport from warm to colder climates.

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