We constructed a new chemical ionization time-of-flight mass spectrometer (CI-TOFMS) that measures atmospheric trace gases in real time with high sensitivity. We apply the technique to the measurement of formic acid via negative-ion proton transfer, using acetate as the reagent ion. A novel high pressure interface, incorporating two RF-only quadrupoles is used to efficiently focus ions through four stages of differential pumping before analysis with a compact TOFMS. The high ion-duty cycle (>20 %) of the TOFMS combined with the efficient production and transmission of ions in the high pressure interface results in a highly sensitive (>300 ions s<sup>−1</sup> pptv<sup>−1</sup> formic acid) instrument capable of measuring and saving complete mass spectra at rates faster than 10 Hz. We demonstrate the efficient transfer and detection of both bare ions and ion-molecule clusters, and characterize the instrument during field measurements aboard the <i>R/V Atlantis</i> as part of the CalNex campaign during the spring of 2010. The in-field short-term precision is better than 5 % at 1 pptv (pL/L), for 1-s averages. The detection limit (3 σ, 1-s averages) of the current version of the CI-TOFMS, as applied to the in situ detection of formic acid, is limited by the magnitude and variability in the background determination and was determined to be 4 pptv. Application of the CI-TOFMS to the detection of other inorganic and organic acids, as well as the use of different reagent ion molecules (e.g. I<sup>−</sup>, CF<sub>3</sub>O<sup>−</sup>, CO<sub>3</sub><sup>−</sup>) is promising, as we have demonstrated efficient transmission and detection of both bare ions and their associated ion-molecule clusters
Abstract.We studied the OH oxidation of submicron aerosol particles consisting of pure palmitic acid (PA) or thin (near monolayer) coatings of PA on aqueous and effloresced inorganic salt particles. Experiments were performed as a function of particle size and OH exposure using a continuousflow photochemical reaction chamber coupled to a chemical ionization mass spectrometer (CIMS) system, for detection of gas and particle-bound organics, and a DMA/CPC for monitoring particle size distributions. The loss rate of PA observed for pure PA aerosols and PA on crystalline NaCl aerosols indicates that the OH oxidation of PA at the gas-aerosol interface is efficient. The pure PA oxidation data are well represented by a model consisting of four main processes: 1) surface-only reactions between OH and palmitic acid, 2) secondary reactions between palmitic acid and OH oxidation products, 3) volatilization of condensedphase mass, and 4) a surface renewal process. Using this model we infer a value of γ OH between 0.8 and 1. The oxidation of palmitic acid in thin film coatings of salt particles is also efficient, though the inferred γ OH is lower, ranging from ∼0.3 (+0.1/−0.05) for coatings on solid NaCl and ∼0.05 (±0.01) on aqueous NaCl particles. These results, together with simultaneous data on particle size change and volatilized oxidation products, provide support for the ideas that oxidative aging of aliphatic organic aerosol is a source of small oxidized volatile organic compounds (OVOCs), and that OH oxidation may initiate secondary condensed-phase reactions.
We present results from a high-resolution chemical ionization time-of-flight mass spectrometer (HRToF-CIMS), operated with two different thermal desorption inlets, designed to characterize the gas and aerosol composition. Data from two field campaigns at forested sites are shown. Particle volatility distributions are estimated using three different methods: thermograms, elemental formulas, and measured partitioning. Thermogram-based results are consistent with those from an aerosol mass spectrometer (AMS) with a thermal denuder, implying that thermal desorption is reproducible across very different experimental setups. Estimated volatilities from the detected elemental formulas are much higher than from thermograms since many of the detected species are thermal decomposition products rather than actual SOA molecules. We show that up to 65% of citric acid decomposes substantially in the FIGAERO-CIMS, with ∼20% of its mass detected as gas-phase CO, CO, and HO. Once thermal decomposition effects on the detected formulas are taken into account, formula-derived volatilities can be reconciled with the thermogram method. The volatility distribution estimated from partitioning measurements is very narrow, likely due to signal-to-noise limits in the measurements. Our findings indicate that many commonly used thermal desorption methods might lead to inaccurate results when estimating volatilities from observed ion formulas found in SOA. The volatility distributions from the thermogram method are likely the closest to the real distributions.
Abstract. During the Biosphere Effects on AeRosols and Photochemistry EXperiment 2007 (BEARPEX-2007), we observed eddy covariance (EC) fluxes of speciated acyl peroxy nitrates (APNs), including peroxyacetyl nitrate (PAN), peroxypropionyl nitrate (PPN) and peroxymethacryloyl nitrate (MPAN), above a Ponderosa pine forest in the western Sierra Nevada. All APN fluxes are net downward during the day, with a median midday PAN exchange velocity of −0.3 cm s −1 ; nighttime storage-corrected APN EC fluxes are smaller than daytime fluxes but still downward. Analysis with a standard resistance model shows that loss of PAN to the canopy is not controlled by turbulent or molecular diffusion. Stomatal uptake can account for 25 to 50% of the observed downward PAN flux. Vertical gradients in the PAN thermal decomposition (TD) rate explain a similar fraction of the flux, suggesting that a significant portion of the PAN flux into the forest results from chemical processes in the canopy. The remaining "unidentified" portion of the net PAN flux (∼15%) is ascribed to deposition or reactive uptake on nonstomatal surfaces (e.g. leaf cuticles or soil). Shifts in temperature, moisture and ecosystem activity during the summerfall transition alter the relative contribution of stomatal uptake, non-stomatal uptake and thermochemical gradients to the net PAN flux. Daytime PAN and MPAN exchange velocities are a factor of 3 smaller than those of PPN during the first two weeks of the measurement period, consistent with strong intra-canopy chemical production of PAN and MPAN Correspondence to: J. A. Thornton (thornton@atmos.washington.edu) during this period. Depositional loss of APNs can be 3-21% of the gross gas-phase TD loss depending on temperature. As a source of nitrogen to the biosphere, PAN deposition represents approximately 4-19% of that due to dry deposition of nitric acid at this site.
15 16 17 18 19 20 21 Keywords 22 Chemical ionization; high-resolution time-of-flight mass spectrometry; atmospheric measurements; 23 analysis of mass spectra; 24 © 2015. This manuscript version is made available under the Elsevier user license
The surface air warming over the Arctic has been almost twice as much as the global average in recent decades. In this region, unprecedented amounts of smoldering peat fires have been identified as a major emission source of climate-warming agents. While much is known about greenhouse gas emissions from these fires, there is a knowledge gap on the nature of particulate emissions and their potential role in atmospheric warming. Here, we show that aerosols emitted from burning of Alaskan and Siberian peatlands are predominantly brown carbon (BrC) -a class of visible lightabsorbing organic carbon (OC) -with a negligible amount of black carbon content. The mean fuel-based emission factors for OC aerosols ranged from 3.8 to 16.6 g kg −1 . Their mass absorption efficiencies were in the range of 0.2-0.8 m 2 g −1 at 405 nm (violet) and dropped sharply to 0.03-0.07 m 2 g −1 at 532 nm (green), characterized by a mean Ångström exponent of ≈ 9. Electron microscopy images of the particles revealed their morphologies to be either single sphere or agglomerated "tar balls". The shortwave top-of-atmosphere aerosol radiative forcing per unit optical depth under clear-sky conditions was estimated as a function of surface albedo. Only over bright surfaces with albedo greater than 0.6, such as snow cover and low-level clouds, the emitted aerosols could result in a net warming (positive forcing) of the atmosphere.Published by Copernicus Publications on behalf of the European Geosciences Union.
Abstract. Hundreds of gas- and particle-phase organic acids were measured in a rural ponderosa pine forest in Colorado, USA, during BEACHON-RoMBAS (Bio-hydro-atmosphere interactions of Energy, Aerosols, Carbon, H2O, Organics & Nitrogen – Rocky Mountain Biogenic Aerosol Study). A recently developed micro-orifice volatilization impactor high-resolution time-of-flight chemical ionization mass spectrometer (MOVI-HRToF-CIMS) using acetate (CH3C(O)O−) as the reagent ion was used to selectively ionize and detect acids semicontinuously from 20 to 30 August 2011, with a measurement time resolution of ~1.5 h. At this site 98% of the organic acid mass is estimated to be in the gas phase, with only ~2% in the particle phase. We investigated gas–particle partitioning, quantified as the fraction in the particle phase (Fp), of C1–C18 alkanoic acids, six known terpenoic acids, and bulk organic acids vs. carbon number. Data were compared to the absorptive partitioning model and suggest that bulk organic acids at this site follow absorptive partitioning to the organic aerosol mass. The rapid response (<1–2 h) of partitioning to temperature changes for bulk acids suggests that kinetic limitations to equilibrium are minor, which is in contrast to conclusions of some recent laboratory and field studies, possibly due to lack of very low ambient relative humidities at this site. Time trends for partitioning of individual and groups of acids were mostly captured by the model, with varying degrees of absolute agreement. Species with predicted substantial fractions in both the gas and particle phases show better absolute agreement, while species with very low predicted fractions in one phase often show poor agreement, potentially due to thermal decomposition, inlet adsorption, or other issues. Partitioning to the aqueous phase is predicted to be smaller than to the organic phase for alkanoic and bulk acids, and has different trends with time and carbon number than observed experimentally. This is due to the limited additional functionalization observed for the bulk acids. Partitioning to water appears to only play a role for the most oxidized acids during periods of high aerosol liquid water. Based on measurement–model comparison we conclude that species carbon number and oxygen content, together with ambient temperature, control the volatility of organic acids and are good predictors for partitioning at this site. Partitioning of bulk acids is more consistent with model predictions for hydroxy acids, hydroperoxyacids, or polyacids, and less so for keto acids.
We describe a new instrument, chemical ionization (CI) highresolution time-of-flight mass spectrometer (ToFMS) coupled to a micro-orifice volatilization impactor (MOVI-HRToF-CIMS).The MOVI-HRToF-CIMS instrument is unique in that, within a compact field-deployable package, it provides (1) quantifiable molecular-level information for both gas and particle-phase organic species on timescales ranging from ≤1 s for gases to 10-60 min for particle-phase compounds that can be used to efficiently probe oxidation and secondary organic aerosol (SOA) formation mechanisms, and (2) relative volatility information of the detected compounds simultaneously estimated using the programmed thermal desorption information obtained from the MOVI. We demonstrate the capabilities of a prototype instrument using known test compounds and complex mixtures generated from the oxidation of biogenic and anthropogenic hydrocarbons. We present spectra obtained using both negative and positive ion CI with acetate (CH 3 C(O)O − ) and protonated water clusters (H 3 O + · (H 2 O) n ), respectively, as reagent ions. The instrument has high mass resolving power (R = 5000 above m/Q 250 Th) and mass accuracy (±20 ppm) enabling estimation of compound elemental composition. Instrument sensitivity in negative ion mode was tested using formic acid as a representative gas-phase compound, and that for particle-phase compounds was tested using palmitic, azelaic, and tricarballylic acids. With a heated MOVI inlet, an ion count rate of ∼15 Hz is achieved when sampling 1 pptv (= 1 pmol/mol) of formic acid (or other monocarboxylic acids) under typical operating conditions. This sensitivity translates to detection limits less than 1 ng/m 3 for carboxylic acids in the particle-phase. We also discuss the remaining challenges with this instrument to broadly characterizing gaseous and particulate oxygenated organic compounds in situ.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.