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| Funder | Swedish Research Council |
|---|---|
| Recipient Organization | University of Gothenburg |
| Country | Sweden |
| Start Date | Jan 01, 2024 |
| End Date | Dec 31, 2027 |
| Duration | 1,460 days |
| Number of Grantees | 2 |
| Roles | Principal Investigator; Co-Investigator |
| Data Source | Swedish Research Council |
| Grant ID | 2023-04520_VR |
The aim is to understand the role of temperature for atmospheric radical chemistry and partitioning of subsequent products under specified chemical regimes.Secondary organic aerosol (SOA) represents a significant portion of the tropospheric aerosol and is crucial for any assessment on air quality or climate change.
Still, there is no adequate mechanistic understanding of SOA formation on a molecular level, and insights have enlightened the need to use a new concept, i.e. chemical regimes, to enhance relevance to ambient atmospheric chemistry. Here the temperature dependence is a key factor for progress in our understanding.
We will utilise our recently develop methods to isolate the chemical regimes in the oxidation of selected VOCs for a range of different temperatures (down to – 30 ℃).
Our new low-temperature flow reactor combined with mass spectrometry will provide the needed capacity to manage these highly advanced experiments. The project will be done within our multi-chamber collaborative frame-work with international partners.
The coordinated experimental and modelling efforts will help us take full benefit of the wealth of complex information in understanding radical chemistry and gas-to-particle transformation forming SOA.The project will provide knowledge from a molecular perspective to promote needed air quality and climate model revisions of relevant atmospheric processes, such as atmospheric chemistry of vapour mixtures and the gas-to-particle transformation
University of Gothenburg
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