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Atmospheric Chemistry and Physics An interactive open-access journal of the European Geosciences Union
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Volume 17, issue 7 | Copyright
Atmos. Chem. Phys., 17, 4433-4450, 2017
© Author(s) 2017. This work is distributed under
the Creative Commons Attribution 3.0 License.

Technical note 03 Apr 2017

Technical note | 03 Apr 2017

Technical note: Relating functional group measurements to carbon types for improved model–measurement comparisons of organic aerosol composition

Satoshi Takahama and Giulia Ruggeri Satoshi Takahama and Giulia Ruggeri
  • ENAC/IIE, Swiss Federal Institute of Technology Lausanne (EPFL), Lausanne, Switzerland

Abstract. Functional group (FG) analysis provides a means by which functionalization in organic aerosol can be attributed to the abundances of its underlying molecular structures. However, performing this attribution requires additional, unobserved details about the molecular mixture to provide constraints in the estimation process. We present an approach for conceptualizing FG measurements of organic aerosol in terms of its functionalized carbon atoms. This reformulation facilitates estimation of mass recovery and biases in popular carbon-centric metrics that describe the extent of functionalization (such as oxygen to carbon ratio, organic mass to organic carbon mass ratio, and mean carbon oxidation state) for any given set of molecules and FGs analyzed. Furthermore, this approach allows development of parameterizations to more precisely estimate the organic carbon content from measured FG abundance. We use simulated photooxidation products of α-pinene secondary organic aerosol previously reported by Ruggeri et al. (2016) and FG measurements by Fourier transform infrared (FT-IR) spectroscopy in chamber experiments by Sax et al. (2005) to infer the relationships among molecular composition, FG composition, and metrics of organic aerosol functionalization. We find that for this simulated system, ∼ 80% of the carbon atoms should be detected by FGs for which calibration models are commonly developed, and ∼ 7% of the carbon atoms are undetectable by FT-IR analysis because they are not associated with vibrational modes in the infrared. Estimated biases due to undetected carbon fraction for these simulations are used to make adjustments in these carbon-centric metrics such that model–measurement differences are framed in terms of unmeasured heteroatoms (e.g., in hydroperoxide and nitrate groups for the case studied in this demonstration). The formality of this method provides framework for extending FG analysis to not only model–measurement but also instrument intercomparisons in other chemical systems.

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We formalize a method for classifying carbon atoms in organic aerosols according to their functionalization. This conceptual approach allows estimation of carbon mass from functional group measurements, which previously required a series of assumptions that were not well constrained. We describe how the proposed strategy can lead to better comparisons among functional group measurements, chemically explicit model simulations, and other measurements.
We formalize a method for classifying carbon atoms in organic aerosols according to their...