Abstract

Abstract. Eleven particle samples collected in the polar stratosphere during SOLVE (SAGE III Ozone loss and validation experiment) from January until March 2000 were characterized in detail by high-resolution transmission and scanning electron microscopy (TEM/SEM) combined with energy-dispersive X-ray microanalysis. A total of 4202 particles (TEM = 3872; SEM = 330) were analyzed from these samples, which were collected mostly inside the polar vortex in the altitude range between 17.3 and 19.9 km. Particles that were volatile in the microscope beams contained ammonium sulfates and hydrogen sulfates and dominated the samples. Some particles with diameters ranging from 20 to 830 nm were refractory in the electron beams. Carbonaceous particles containing additional elements to C and O comprised from 72 to 100 % of the refractory particles. The rest were internal mixtures of these materials with sulfates. The median number mixing ratio of the refractory particles, expressed in units of particles per milligram of air, was 1.1 (mg air)−1 and varied between 0.65 and 2.3 (mg air)−1. Most of the refractory carbonaceous particles are completely amorphous, a few of the particles are partly ordered with a graphene sheet separation distance of 0.37 ± 0.06 nm (mean value ± standard deviation). Carbon and oxygen are the only detected major elements with an atomic O∕C ratio of 0.11 ± 0.07. Minor elements observed include Si, S, Fe, Cr and Ni with the following atomic ratios relative to C: Si∕C: 0.010 ± 0.011; S∕C: 0.0007 ± 0.0015; Fe∕C: 0.0052 ± 0.0074; Cr∕C: 0.0012 ± 0.0017; Ni∕C: 0.0006 ± 0.0011 (all mean values ± standard deviation).High-resolution element distribution images reveal that the minor elements are distributed within the carbonaceous matrix; i.e., heterogeneous inclusions are not observed. No difference in size, nanostructure and elemental composition was found between particles collected inside and outside the polar vortex. Based on chemistry and nanostructure, aircraft exhaust, volcanic emissions and biomass burning can certainly be excluded as sources. The same is true for the less probable but globally important sources: wood burning, coal burning, diesel engines and ship emissions. Recondensed organic matter and extraterrestrial particles, potentially originating from ablation and fragmentation, remain as possible sources of the refractory carbonaceous particles studied. However, additional work is required in order to identify the sources unequivocally.

Highlights

  • The chemistry of stratospheric aerosols has been studied for more than half a century (Junge et al, 1961; Junge, 1963), and it was discovered that sulfur is the main element in the particles. Junge and Manson (1961) supposed the particles to consist of ammonium sulfate, and Bigg et al (1970) suggested sulfuric acid with varying amounts of ammonia.Published by Copernicus Publications on behalf of the European Geosciences Union.K

  • Element distribution images were acquired with a JEOL JEM 2100F (JEOL, Tokyo, Japan) operated in scanning transmission electron microscopy (STEM) mode at an electron acceleration voltage of 200 kV

  • As TEM brightfield images show (Fig. 1), volatile particles cover a relatively larger area compared to refractory particles

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Summary

Introduction

The chemistry of stratospheric aerosols has been studied for more than half a century (Junge et al, 1961; Junge, 1963), and it was discovered that sulfur is the main element in the particles. Junge and Manson (1961) supposed the particles to consist of ammonium sulfate, and Bigg et al (1970) suggested sulfuric acid with varying amounts of ammonia.K. The chemistry of stratospheric aerosols has been studied for more than half a century (Junge et al, 1961; Junge, 1963), and it was discovered that sulfur is the main element in the particles. Junge and Manson (1961) supposed the particles to consist of ammonium sulfate, and Bigg et al (1970) suggested sulfuric acid with varying amounts of ammonia. Rosen (1971) strengthened the evidence for the material to be sulfuric acid as most of the material evaporated at the temperature expected for this substance. According to Bigg (1975), the majority of the particles is composed of sulfuric acid with varying amounts of ammonium sulfate. A comprehensive summary of stratospheric aerosol and sulfur chemistry is given by Kremser et al (2016)

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