Dust particulates play an essential role for the nucleation, hygroscopicity and also contribute to aerosol mass. We investigated the chemical composition, size distribution and mixing states of PM_2.5 using a single-particle aerosol mass spectrometer (SPAMS), Monitor for AeRosols and Gases (MARGA), and off-line membrane sampling from 2018.1.24 to 2018.2.20 at a coastal supersite in Ningbo, a port city in Yangtze River Delta, China. During the study campaign, the eastern part of China had experienced a wide range of cooling, sandstorm, and snowfall processes. The entire sampling campaign was categorized into five sub-periods based on the levels of PM_2.5 and the ratios of PM_2.5/PM10, namely clean (T1), heavy pollution (T2), light pollution (T3), dust (sandstorm) (T4) and cleaning pollution (T5) period. After comparing the average mass spectrum for each period, it shows that the primary ions, such as Ca²⁺and SiO^3-, rarely coexist with each other within a single particle, but secondary ions generally coexist with these primary ions. Furthermore, the coexistence of each two different ions within a particle does not show distinct variation for the whole study periods. All these suggest that the absorption and partitioning of gaseous contaminants into the surface of primary aerosol through heterogeneous reactions are the major pathways of aging and growth of aerosol; and the merging of particles through collisions usually is insignificant. Although the absolute concentrations of nitrate and sulfate all increased with the PM_2.5 concentrations, the relative equivalent concentrations of NO^3- and SO₄^2- displayed opposite trends; the relative contribution of sulfate decreased and that of nitrate increased as the increase of pollution. During the dust period, the relative equivalent concentrations of calcium and/or potassium ions in PM_2.5 are significantly higher. This study provided deep insights about the mixing states and characteristics of particulate after long-range transport and a visualization tool for aerosol study.

The sampling site