Isoprene Epoxydiols as Precursors to Secondary Organic Aerosol Formation: Acid-Catalyzed Reactive Uptake Studies with Authentic Standards

Lin, YH; Zhang, Z; Docherty, KS; Zhang, H; Budisulistiorini, SH; Rubitschun, CL; Shaw, S; Knipping, E; Edgerton, ES; Kleindienst, TE; Gold, A; Surratt, JD

HERO ID

863786

Reference Type

Journal Article

Year

2012

Language

English

PMID

22103348

HERO ID 863786
In Press No
Year 2012
Title Isoprene Epoxydiols as Precursors to Secondary Organic Aerosol Formation: Acid-Catalyzed Reactive Uptake Studies with Authentic Standards
Authors Lin, YH; Zhang, Z; Docherty, KS; Zhang, H; Budisulistiorini, SH; Rubitschun, CL; Shaw, S; Knipping, E; Edgerton, ES; Kleindienst, TE; Gold, A; Surratt, JD
Journal Environmental Science & Technology
Volume 46
Issue 1
Page Numbers 250-258
Abstract Isoprene epoxydiols (IEPOX), formed from the photooxidation of isoprene under low-NOx conditions, have recently been proposed as precursors of secondary organic aerosol (SOA) on the basis of mass spectrometric evidence. In the present study, IEPOX isomers were synthesized in high purity (> 99%) to investigate their potential to form SOA via reactive uptake in a series of controlled dark chamber studies followed by reaction product analyses. IEPOX-derived SOA was substantially observed only in the presence of acidic aerosols, with conservative lower-bound yields of 4.7-6.4% for β-IEPOX and 3.4-5.5% for δ-IEPOX, providing direct evidence for IEPOX isomers as precursors to isoprene SOA. These chamber studies demonstrate that IEPOX uptake explains the formation of known isoprene SOA tracers found in ambient aerosols, including 2-methyltetrols, C5-alkene triols, dimers, and IEPOX-derived organosulfates. Additionally, we show reactive uptake on the acidified sulfate aerosols supports a previously unreported acid-catalyzed intramolecular rearrangement of IEPOX to cis- and trans-3-methyltetrahydrofuran-3,4-diols (3-MeTHF-3,4-diols) in the particle phase. Analysis of these novel tracer compounds by aerosol mass spectrometry (AMS) suggests that they contribute to a unique factor resolved from positive matrix factorization (PMF) of AMS organic aerosol spectra collected from low-NOx, isoprene-dominated regions influenced by the presence of acidic aerosols.
Doi 10.1021/es202554c
Pmid 22103348
Wosid WOS:000298762900035
Is Certified Translation No
Dupe Override No
Comments Source: Web of Science WOS:000298762900035
Is Public Yes
Language Text English
Is Qa No