Oxidation flow reactors (OFRs) efficiently produce OH radicals using low-pressure Hg-lamp emissions at λ = 254 nm (OFR254) or both λ = 185 and 254 nm (OFR185). OFRs under most conditions are limited to studying low-NO chemistry (where RO 2 + HO 2 dominates RO 2 fate), even though substantial amounts of initial NO may be injected. This is due to very fast NO oxidation by high concentrations of OH, HO 2, and O 3 . In this study, we model new techniques for maintaining high-NO conditions in OFRs, that is, continuous NO addition along the length of the reactor in OFR185 (OFR185-cNO), recently proposed injection of N 2 O at the entrance of the reactor in OFR254 (OFR254-iN 2 O), and an extension of that idea to OFR185 (OFR185-iN 2 O). For these techniques, we evaluate (1) fraction of conditions dominated by RO 2 + NO while avoiding significant nontropospheric photolysis and (2) fraction of conditions where reactions of precursors with OH dominate over unwanted reactions with NO 3 . OFR185-iN 2 O is the most practical for general high-NO experiments because it represents the best compromise between experimental complexity and performance upon proper usage. Short lamp distances are recommended for OFR185-iN 2 O to ensure a relatively uniform radiation field. OFR185-iN 2 O with low O 2 or using Hg lamps with higher 185 nm-to-254 nm ratio can improve performance. OFR185-iN 2 O experiments should generally be conducted at higher relative humidity, higher UV, lower concentration of non-NO y external OH reactants, and percent-level N 2 O. OFR185-cNO and OFR185-iN 2 O at optimal NO precursor injection rate (∼2 ppb/s) or concentration (∼3%) would have satisfactory performance in typical field studies where ambient air is oxidized. Exposure estimation equations are provided to aid experimental planning. This work enables improved high-NO OFR experimental design and interpretation.
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Peng et al. (2017) studied this question.