Yields of Carbonyl Products from Gas-Phase Reactions of Fragrance Compounds with OH Radical and Ozone
journal contributionposted on 15.05.2009, 00:00 by Crystal D. Forester, J. Raymond Wells
Chamber studies to quantify formation yields of oxygenated organic reaction products were performed for gas-phase reactions of the hydroxyl radical (OH·) and ozone (O3) with the common cleaning product terpene compounds limonene, α-terpineol, and geraniol. The reaction products observed were identified and quantified using derivatization by O-(2,3,4,5,6-pentafluorobenzyl)hydroxylamine (PFBHA) and gas chromatography/mass spectrometry. Limonene rate constants and product mechanisms have been examined previously. Several of these investigations have measured product yields from limonene reactions and those results are compared with the results presented here. Although rate constants and product mechanisms have previously been investigated for α-terpineol and geraniol, yields of oxygenated organic reaction products have not been measured. Reactions from the fragrance compounds in this study produced several dicarbonyl reaction products such as glyoxal, methylglyoxal, and 4-oxopentanal which were observed from all three terpenes. Total carbonyl yields ranged from 5.1% for the limonene + O3 reaction to 92% for the geraniol + O3 reaction.