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Title: Brown carbon formation from ketoaldehydes of biogenic monoterpenes

Journal Article · · Faraday Discussions, 165:473-494
DOI:https://doi.org/10.1039/c3fd00036b· OSTI ID:1117068

Sources and chemical composition of the brown carbon are poorly understood, and even less is known about the mechanisms of its atmospheric transformations. This work presents molecular level investigation of the reactive compound ketolimononaldehyde (KLA, C9H14O3), a second generation ozonolysis product of limonene (C10H16), as a potent brown carbon precursor in secondary organic aerosol (SOA) through its reactions with reduced nitrogen compounds such as ammonium ion (NH4+), ammonia, and amino acids. The reactions of synthesized and purified KLA with NH4+ and glycine resulted in the formation of chromophores nearly identical in spectral properties and formation rates to those found in similarly-aged limonene/O3 SOA. Similar chemical reaction processes of limononaldehyde (LA, C10H16O2) and pinonaldehyde (PA, C10H16O2), the first-generation ozonolysis products in the oxidation of limonene and α-pinene, respectively, were also studied, but the resulting products did not exhibit light absorption properties of brown carbon, suggesting that the unique molecular structure of KLA produces visible-light-absorbing compounds. The KLA/NH4+ and KLA/GLY reactions produce water-soluble, hydrolysis-resilient chromophores with high mass absorption coefficients (MAC = 2000-4000 cm2 g-1) at λ ~ 500 nm, precisely at the maximum of the solar emission spectrum. Liquid chromatography was used to isolate the light-absorbing fraction, and UV-Vis, FTIR, NMR and high-resolution mass spectrometry (HR-MS) techniques were used to investigate the structures and chemical properties of the light-absorbing compounds. The KLA browning reaction generates a diverse mixture of light-absorbing compounds, with the majority of the observable products containing 1-4 units of KLA and 0-2 nitrogen atoms. Based on the HR-MS product distribution, conjugated aldol condensates, secondary imines (Schiff bases), and N-heterocycles like pyrroles may contribute in varying degree to the light-absorbing properties of the KLA brown carbon. Results of this study demonstrate the high degree of selectivity and the effect a specific organic compound on the light-absorbing properties of SOA.

Research Organization:
Pacific Northwest National Lab. (PNNL), Richland, WA (United States). Environmental Molecular Sciences Lab. (EMSL)
Sponsoring Organization:
USDOE
DOE Contract Number:
AC05-76RL01830
OSTI ID:
1117068
Report Number(s):
PNNL-SA-94365; 44638; 39957; KP1704020; KC0302020
Journal Information:
Faraday Discussions, 165:473-494, Journal Name: Faraday Discussions, 165:473-494
Country of Publication:
United States
Language:
English

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