Secondary aerosol formation through photochemical reactions estimated by using air quality monitoring data in Taipei City from 1994 to 2003

Analyses of diurnal patterns of PM₁₀ in Taipei City have been performed in this study at different daily ozone maximum concentrations (O_3,max) from 1994 to 2003. In order to evaluate secondary aerosol formation at different ozone levels, CO was used as a tracer of primary aerosol, and O_3,max was used as an index of photochemical activity. Results show that when O_3,max exceeds 120 ppb, the highest photochemical formation of secondary aerosol can be found at 15:00 (local time). The produced secondary aerosol is estimated to contribute 30 μg m^-3 (43%) of PM₁₀ concentration, and about 77% of the estimated secondary PM₁₀ is composed of PM_2.5. The estimated maximum concentration of secondary aerosol occurs 2-3 h later than the maximum ozone concentration. As revealed in an O₃ episode, PM₁₀ and PM_2.5 vary consistently with O₃ at daytime, which suggests that they are mostly secondary aerosols produced from photochemical reactions. Data collected from Taipei aerosol supersite in 2002 indicates that for all O₃ levels, summertime PM_2.5 is composed of 23%, 20%, 9%, and 7% of organic carbon, sulfate, nitrate, and elemental carbon, respectively. Aerosol number and volume size spectra are dominated by submicron particles either from pollution transport or photochemical reactions. Secondary PM₁₀ concentrations show increasing tendencies for the time between 15:00 and 19:00 from 1994-1996 to 2001-2003. This reveals that the abatement of secondary PM₁₀ becomes more important after pronounced primary PM₁₀ reduction in a metropolis.