Abstract

Abstract. Particle size distribution down to 1.4 nm was measured in the urban atmosphere of Nanjing, China, in spring, summer, and winter during 2014–2015. Sub-3 nm particle event, which is equivalent to nucleation event, occurred on 42 out of total 90 observation days, but new particles could grow to cloud condensation nuclei (CCN)-active sizes on only 9 days. In summer, infrequent nucleation was limited by both unfavorable meteorological conditions (high temperature and relative humidity – RH) and reduced anthropogenic precursor availability due to strict emission control measures during the 2014 Youth Olympic Games in Nanjing. The limiting factors for nucleation in winter and spring were meteorological conditions (radiation, temperature, and RH) and condensation sink, but for the further growth of sub-3 nm particles to CCN-active sizes, anthropogenic precursors again became limiting factors. Nucleation events were strong in the polluted urban atmosphere. Initial J1.4 at the onset and peak J1.4 at the noontime could be up to 2.1 × 102 and 2.5 × 103 cm−3 s−1, respectively, during the eight nucleation events selected from different seasons. Time-dependent J1.4 usually showed good linear correlations with a sulfuric acid proxy for every single event (R2 = 0.56–0.86, excluding a day with significant nocturnal nucleation), but the correlation among all eight events deteriorated (R2 = 0.17) due to temperature or season change. We observed that new particle growth rate (GR) did not increase monotonically with particle size, but had a local maximum up to 25 nm h−1 between 1 and 3 nm. The existence of local maxima GR in sub-3 nm size range, though sensitive to measurement uncertainties, gives new insight into cluster dynamics in polluted environments. In this study such growth rate behavior was interpreted as the solvation effect of organic activating vapor in newly formed inorganic nuclei.

Highlights

  • New particle formation (NPF) is an important source of secondary aerosols in the atmosphere (Kulmala et al, 2004a)

  • With our instrument capability in this work, we could not deduce any valuable information on the nocturnal nucleation mechanism, except that we found that the air mass on 4 March was relatively clean, and temperature and relative humidity (RH) were favorable for nucleation

  • NPF can contribute to cloud condensation nuclei (CCN) only after going through nucleation, initial growth steps, and subsequent growth to CCNactive sizes

Read more

Summary

Introduction

New particle formation (NPF) is an important source of secondary aerosols in the atmosphere (Kulmala et al, 2004a). NPF is a two-stage process consisting of the formation of clusters and subsequent growth to detectable sizes (Kulmala et al, 2000). Chamber experiments have made substantial progress in revealing the fundamental processes involved in particle nucleation and growth (Kirkby et al, 2011; Almeida et al, 2013; Schobesberger et al, 2013; Riccobono et al, 2014; Ehn et al, 2014; Kürten et al, 2014). The identity and physico-chemical properties of assisting vapors other than sulfuric acid (H2SO4) are uncertain so far. It is uncertain what mechanisms allow for the assisting vapors to over-

Objectives
Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call