Eleanor M. Waxman

Modeling the weekly cycle of NOx and CO emissions and their impacts on O3 in the Los Angeles‐South Coast Air Basin during the CalNex 2010 field campaign

We developed a new nitrogen oxide (NOx) and carbon monoxide (CO) emission inventory for the Los Angeles-South Coast Air Basin (SoCAB) expanding the Fuel-based Inventory for motor-Vehicle Emissions and applied it in regional chemical transport modeling focused on the California Nexus of Air Quality and Climate Change (CalNex) 2010 field campaign. The weekday NOx emission over the SoCAB in 2010 is 620 t d−1, while the weekend emission is 410 t d−1. The NOx emission decrease on weekends is caused by reduced diesel truck activities. Weekday and weekend CO emissions over this region are similar: 2340 and 2180 t d−1, respectively. Previous studies reported large discrepancies between the airborne observations of NOx and CO mixing ratios and the model simulations for CalNex based on the available bottom-up emission inventories. Utilizing the newly developed emission inventory in this study, the simulated NOx and CO mixing ratios agree with the observations from the airborne and the ground-based in situ and remote sensing instruments during the field study. The simulations also reproduce the weekly cycles of these chemical species. Both the observations and the model simulations indicate that decreased NOx on weekends leads to enhanced photochemistry and increase of O3 and Ox (=O3 + NO2) in the basin. The emission inventory developed in this study can be extended to different years and other urban regions in the U.S. to study the long-term trends in O3 and its precursors with regional chemical transport models.

Measurements of hydroxyl and hydroperoxy radicals during CalNex‐LA: Model comparisons and radical budgets

Measurements of hydroxyl (OH) and hydroperoxy (HO2*) radical concentrations were made at the Pasadena ground site during the CalNex-LA 2010 campaign using the laser-induced fluorescence-fluorescence assay by gas expansion technique. The measured concentrations of OH and HO2* exhibited a distinct weekend effect, with higher radical concentrations observed on the weekends corresponding to lower levels of nitrogen oxides (NOx). The radical measurements were compared to results from a zero-dimensional model using the Regional Atmospheric Chemical Mechanism-2 constrained by NOx and other measured trace gases. The chemical model overpredicted measured OH concentrations during the weekends by a factor of approximately 1.4 ± 0.3 (1σ), but the agreement was better during the weekdays (ratio of 1.0 ± 0.2). Model predicted HO2* concentrations underpredicted by a factor of 1.3 ± 0.2 on the weekends, while measured weekday concentrations were underpredicted by a factor of 3.0 ± 0.5. However, increasing the modeled OH reactivity to match the measured total OH reactivity improved the overall agreement for both OH and HO2* on all days. A radical budget analysis suggests that photolysis of carbonyls and formaldehyde together accounted for approximately 40% of radical initiation with photolysis of nitrous acid accounting for 30% at the measurement height and ozone photolysis contributing less than 20%. An analysis of the ozone production sensitivity reveals that during the week, ozone production was limited by volatile organic compounds throughout the day during the campaign but NOx limited during the afternoon on the weekends.

Gas-phase broadband spectroscopy using active sources: progress, status, and applications [Invited]

Broadband spectroscopy is an invaluable tool for measuring multiple gas-phase species simultaneously. In this work we review basic techniques, implementations, and current applications for broadband spectroscopy. We discuss components of broad-band spectroscopy including light sources, absorption cells, and detection methods and then discuss specific combinations of these components in commonly-used techniques. We finish this review by discussing potential future advances in techniques and applications of broad-band spectroscopy.

Computational study of the effect of glyoxal-sulfate clustering on the Henry's law coefficient of glyoxal.

We have used quantum chemical methods to investigate the molecular mechanism behind the recently reported ( Kampf , C. J. ; Environ. Sci. Technol . 2013 , 47 , 4236 - 4244 ) strong dependence of the Henrys law coefficient of glyoxal (C2O2H2) on the sulfate concentration of the aqueous phase. Although the glyoxal molecule interacts only weakly with sulfate, its hydrated forms (C2O3H4 and C2O4H6) form strong complexes with sulfate, displacing water molecules from the solvation shell and increasing the uptake of glyoxal into sulfate-containing aqueous solutions, including sulfate-containing aerosol particles. This promotes the participation of glyoxal in reactions leading to secondary organic aerosol formation, especially in regions with high sulfate concentrations. We used our computed equilibrium constants for the complexation reactions to assess the magnitude of the Henrys law coefficient enhancement and found it to be in reasonable agreement with experimental results. This indicates that the complexation of glyoxal hydrates with sulfate can explain the observed uptake enhancement.

Open-path dual-comb spectroscopy to an airborne retroreflector

We demonstrate a new technique for spatial mapping of multiple atmospheric gas species. This system is based on high-precision dual-comb spectroscopy to a retroreflector mounted on a flying multi-copter. We measure the atmospheric absorption over long open-air paths to the multi-copter with comb-tooth resolution over 1.57 to 1.66 pm, covering absorption bands of CO2, Cm, H2O and isotopologues. When combined with GPS-based path length measurements, a fit of the absorption spectra retrieves the dry mixing ratios versus position. Under well-mixed atmospheric conditions, retrievals from both horizontal and vertical paths show stable mixing ratios as expected. This approach can support future boundary layer studies as well as plume detection and source location.

Simulation of semi-explicit mechanisms of SOA formation from glyoxal in a 3-D model

Christoph Knote1), Alma Hodzic1), Jose L. Jimenez2,3), Rainer Volkamer2,3), Sunil Baidar2,3), Jerome Brioude3,5), Jerome Fast4), Jessica B. Gilman3,5), Allen Goldstein9), Joost de Gouw3,5), Patrick Hayes2,3), B. Tom Jobson6), W. Berk Knighton7), William C. Kuster3,5), Hilke Oetjen8), John Orlando1), Chen Song4), Harald Stark3,5), Philip S. Stevens10), Ryan Thalman2,3), Geoff Tyndall1), Carsten Warneke3,5), Rebecca Washenfelder3,5), Eleanor Waxman2,3), Qi Zhang11)

Regional sensing with an open-path dual comb spectroscopy and a UAS (Conference Presentation)

The output of a laser frequency comb is composed of 100,000+ perfectly spaced, discrete wavelength elements or comb teeth, that act as a massively parallel set of single frequency (CW) lasers with highly stable, well-known frequencies. In dual-comb spectroscopy, two such frequency combs are interfered on a single detector yielding absorption information for each individual comb tooth. This approach combines the strengths of both cw laser spectroscopy and broadband spectroscopy providing high spectral resolution and broad optical bandwidths, all with a single-mode, high-brightness laser beam and a simple, single photodetector, detection scheme. Here we show that this novel spectroscopy source can be employed for regional (~kilometer squared) monitoring using an array of stationed retros or in conjunction with an unmanned aerial systems (UAS). Both fixed and UAS systems combine the high-precision, multi-species detection capabilities of open-path DCS with the spatial scanning capabilities to enable spatial mapping of atmospheric gas concentrations. The DCS systems measure the atmospheric absorption over long, 100m to 1 km, open air paths with 0.007cm-1 resolution over 1.57 to 1.66 um, covering absorption bands of CO2, CH4, H2O and isotopologues.

Estimating vehicle carbon dioxide emissions from Boulder, Colorado using horizontal path-integrated column measurements

We performed 7.5 weeks of path-integrated concentration measurements of CO2, CH4, H2O, and HDO over the city of Boulder, Colorado. An open-path dual-comb spectrometer simultaneously measured time-resolved data across a reference path, located near the mountains to the west of the city, and across an over-city path that intersected two-thirds of the city, including two major commuter arteries. By comparing the measured concentrations over the two paths when the wind is primarily out of the west, we observe daytime CO2 enhancements over the city. Given the warm weather and the measurement footprint, the dominant contribution to the CO2 enhancement is from city vehicle traffic. We use a Gaussian plume model combined with reported city traffic patterns to estimate city emissions of on-road CO2 as (6.2 ± 2.2) × 105 metric tons (t) CO2 yr−1 after correcting for non-traffic sources. Within the uncertainty, this value agrees with the city’s bottom-up greenhouse gas inventory for the on-road vehicle sector of 4.5 × 105 t CO2 yr−1. Finally, we discuss experimental modifications that could lead to improved estimates from our path-integrated measurements.

Can COSMOTherm Predict a Salting in Effect

We have used COSMO-RS, a method combining quantum chemistry with statistical thermodynamics, to compute Setschenow constants (KS) for a large array of organic solutes and salts. These comprise both atmospherically relevant solute-salt combinations, as well as systems for which experimental data are available. In agreement with previous studies on single salts, the Setschenow constants predicted by COSMO-RS (as implemented in the COSMOTherm program) are generally too large compared to experiments. COSMOTherm overpredicts salting out (positive KS), and/or underpredicts salting in (negative KS). For ammonium and sodium salts, KS values are larger for oxalates and sulfates, and smaller for chlorides and bromides. For chloride and bromide salts, KS values usually increase with decreasing size of the cation, along the series Pr4N+ < Et4N+ < Me4N+ ≤ Na+ ≈ NH4+. Of the atmospherically relevant systems studied, salting in is predicted only for oxalic acid in sodium and ammonium oxalate, and sodium sulfate, solutions. COSMOTherm was thus unable to replicate the experimentally observed salting in of glyoxal in sulfate solutions, likely due to the overestimation of salting out effects. By contrast, COSMOTherm does qualitatively predict the experimentally observed salting in of multiple organic solutes in solutions of alkylaminium salts.

Dual-Comb spectroscopy for GHG quantification

Near-infrared frequency-comb spectroscopy is a powerful tool with which to measure concentrations of gasses relevant to combustion and atmospheric monitoring (CO2, CH4, H2O, HDO) over meter and kilometer scale paths.