<?xml version="1.0" encoding="UTF-8"?><rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcq="http://purl.org/dc/terms/"><records count="1" morepages="false" start="1" end="1"><record rownumber="1"><dc:product_type>Conference Paper</dc:product_type><dc:title>Isoprene Epoxydiol-Derived Sulfated and Non-Sulfated Oligomers Suppress Particulate Mass Loss during Oxidative Aging of Secondary Organic Aerosol</dc:title><dc:creator>ARMSTRONG, N. CAZIMIR; Chen, Yuzh; Cui, Tianqu; Zhang, Yue; Zhang, Zhenfa; Turpin, Barbara; Chan, Man Nin; Gold, Avram; Ault, Andrew; Surratt, Jason</dc:creator><dc:corporate_author/><dc:editor/><dc:description>Acid-driven multiphase chemistry of isoprene epoxydiols (IEPOX) with inorganic sulfate aerosols contributes substantially to formation of secondary organic aerosol (SOA), which constitutes a large mass fraction of atmospheric fine particulate matter (PM2.5). However, atmospheric chemical sinks of freshly generated IEPOX-SOA particles remain unclear. We examined the role of heterogeneous oxidation of freshly-generated IEPOX-SOA particles by gas-phase hydroxyl radical (•OH) under dark conditions as one potential atmospheric sink. After 4 h of gas-phase •OH exposure (~3x108 molecules cm-3), chemical changes in smog chamber-generated IEPOX-SOA particles were assessed by hydrophilic interaction liquid chromatography coupled with electrospray ionization high-resolution quadrupole time-of-flight mass spectrometry (HILIC/ESI-HR-QTOFMS). Comparison of molecular-level compositional changes in IEPOX-SOA particles during aging with or without •OH revealed that decomposition of oligomers by heterogeneous •OH oxidation acts as a sink for •OH and maintains a reservoir of low-volatility compounds including monomeric sulfate esters and oligomer fragments. We propose tentative structures and formation mechanisms for previously uncharacterized SOA constituents in PM2.5. Our results suggest that this •OH-driven renewal of low-volatility products may extend atmospheric lifetimes of IEPOX-SOA particles by slowing production of low-molecular weight, high-volatility organic fragments, and likely contributes to large quantities of 2-methyltetrols and methyltetrol sulfates reported in PM2.5.</dc:description><dc:publisher/><dc:date>2022-10-01</dc:date><dc:nsf_par_id>10392011</dc:nsf_par_id><dc:journal_name>AAAR 40th Annual Conference</dc:journal_name><dc:journal_volume/><dc:journal_issue/><dc:page_range_or_elocation/><dc:issn/><dc:isbn/><dc:doi>https://doi.org/</dc:doi><dcq:identifierAwardId>2001027</dcq:identifierAwardId><dc:subject/><dc:version_number/><dc:location/><dc:rights/><dc:institution/><dc:sponsoring_org>National Science Foundation</dc:sponsoring_org></record></records></rdf:RDF>