State transformations and ice nucleation in amorphous (semi-)solid organic aerosol
Amorphous (semi-)solid organic aerosol particles have the potential to serve as surfaces for heterogeneous ice nucleation in cirrus clouds. Raman spectroscopy and optical microscopy have been used in conjunction with a cold stage to examine water uptake and ice nucleation on individual amorphous (se...
| Main Authors: | , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Copernicus Publications
2013-06-01
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| Series: | Atmospheric Chemistry and Physics |
| Online Access: | http://www.atmos-chem-phys.net/13/5615/2013/acp-13-5615-2013.pdf |
| Summary: | Amorphous (semi-)solid organic aerosol particles have the potential to serve as surfaces for heterogeneous ice nucleation in cirrus clouds. Raman spectroscopy and optical microscopy have been used in conjunction with a cold stage to examine water uptake and ice nucleation on individual amorphous (semi-)solid particles at atmospherically relevant temperatures (200–273 K). Three organic compounds considered proxies for atmospheric secondary organic aerosol (SOA) were used in this investigation: sucrose, citric acid and glucose. Internally mixed particles consisting of each organic and ammonium sulfate were also investigated. <br><br> Results from water uptake experiments followed the shape of a humidity-induced glass transition (<i>T</i><sub>g</sub>(RH)) curve and were used to construct state diagrams for each organic and corresponding mixture. Experimentally derived <i>T</i><sub>g</sub>(RH) curves are in good agreement with theoretical predictions of <i>T</i><sub>g</sub>(RH) following the approach of Koop et al. (2011). A unique humidity-induced glass transition point on each state diagram, <i>T</i><sub>g</sub>'(RH), was used to quantify and compare results from this study to previous works. Values of <i>T</i><sub>g</sub>'(RH) determined for sucrose, glucose and citric acid glasses were 236, 230 and 220 K, respectively. Values of <i>T</i><sub>g</sub>'(RH) for internally mixed organic/sulfate particles were always significantly lower; 210, 207 and 215 K for sucrose/sulfate, glucose/sulfate and citric acid/sulfate, respectively. <br><br> All investigated SOA proxies were observed to act as heterogeneous ice nuclei at tropospheric temperatures. Heterogeneous ice nucleation on pure organic particles occurred at <i>S</i><sub>ice</sub> = 1.1–1.4 for temperatures below 235 K. Particles consisting of 1:1 organic-sulfate mixtures took up water over a greater range of conditions but were in some cases also observed to heterogeneously nucleate ice at temperatures below 202 K (<i>S</i><sub>ice</sub>= 1.25–1.38). <br><br> Polynomial curves were fitted to experimental water uptake data and then incorporated into the Community Aerosol Radiation Model for Atmospheres (CARMA) along with the predicted range of humidity-induced glass transition temperatures for atmospheric SOA from Koop et al. (2011). Model results suggest that organic and organic/sulfate aerosol could be glassy more than 60% of the time in the midlatitude upper troposphere and more than 40% of the time in the tropical tropopause region (TTL). At conditions favorable for ice formation (<i>S</i><sub>ice</sub> > 1), particles in the TTL are expected to be glassy more than 50% of the time for temperatures below 200 K. Results from this study suggests that amorphous (semi-)solid organic particles are often present in the upper troposphere and that heterogeneous ice formation on this type of particle may play an important role in cirrus cloud formation. |
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| ISSN: | 1680-7316 1680-7324 |