China, the world’s largest consumer of coal, emits approximately 30 million tons of sulfur dioxide (SO2) per year. SO2 is subsequently oxidized to sulfate in the atmosphere. However, large gaps exist between model-predicted and measured sulfate levels in China. Long-term ?eld observations and numerical simulations were integrated to investigate the effect of mineral aerosols on sulfate formation. We found that mineral aerosols contributed a nationwide average of approximately 22% to sulfate production in 2006. The increased sulfate concentration was approximately 2 µgm À3 in the entire China. In East China and the Sichuan Basin, the increments reached 6.3 µgm À3 and 7.3 µgm À3, respectively. Mineral aerosols led to faster SO2 oxidation through three pathways. First, more SO2 was dissolved as cloud water alkalinity increased due to water-soluble mineral cations. Sulfate produc tion was then enhanced through the aqueous-phase oxidation of S(IV) (dissolved sulfur in oxidation state +4). The contribution to the national sulfate productio n was 5%. Second, sulfate was enhanced through S(IV) cataly zed oxi dation by transition metals. The contribution to the annual sulfate produc tion was 8%, with 19% during the winter that decreased to 2% during the summer. Third, SO2 reacts on the sur face of mineral aerosols to produce sulfate. The contribution to the national average sulfate concentration was 9% with 16% during the winter and a negligible effect d uring the summer. Th e i nclusion of mineral aer os ols does reso lve model discrepancies with sulfate observations in China, especially during the winter. These three pathways, which are not fully c on sidered in most current chemistry-climate models, will signi?cantly impact asses sments regarding the effects o f aerosol on climate change in China.
Revised: June 24, 2015 |
Published: December 27, 2014
Citation
Huang X., Y. Song, C. Zhao, M. Li, T. Zhu, Q. Zhang, and X. Zhang. 2014.Pathways of sulfate enhancement by natural and anthropogenic mineral aerosols in China.Journal of Geophysical Research: Atmospheres 119, no. 24:14,165–14,179.PNNL-SA-108380.doi:10.1002/2014JD022301