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Abstract
Ship engines in the open ocean and Arctic typically combust heavy fuel oil (HFO), resulting in light-absorbing particulate matter (PM) emissions that have been attributed to black carbon (BC) and conventional, soluble brown carbon (brC). We show here that neither BC nor soluble brC is the major light-absorbing carbon (LAC) species in HFO-combustion PM. Instead, “tar brC” dominates. This tar brC, previously identified only in open-biomass-burning emissions, shares key defining properties with BC: it is insoluble, refractory, and substantially absorbs visible and near-infrared light. Relative to BC, tar brC has a higher Angstrom absorption exponent (AAE) (2.5–6, depending on the considered wavelengths), a moderately-high mass absorption efficiency (up to 50% of that of BC), and a lower ratio of sp2- to sp3-bonded carbon. Based on our results, we present a refined classification of atmospheric LAC into two sub-types of BC and two sub-types of brC. We apply this refined classification to demonstrate that common analytical techniques for BC must be interpreted with care when applied to tar-containing aerosols. The global significance of our results is indicated by field observations which suggest that tar brC already contributes to Arctic snow darkening, an effect which may be magnified over upcoming decades as Arctic shipping continues to intensify.
Atmospheric Science: Shipping Emissions
Ship emissions are dominated by a different type of particle than once thought. Ships typically use heavy fuel oil for combustion, releasing small light-absorbing particles such as black and brown carbon (brC). However, the properties and composition of such ship-related carbonaceous emissions is not well-known, complicating the quantification of their climatic impacts. Using various analytical techniques, Joel Corbin from the Paul Scherrer Institute, Switzerland and National Research Council Canada, and colleagues, demonstrate that light-absorbing particulates from heavy fuel oil are dominated by tar brC, an insoluble particulate with strong absorbance in the near infrared, previously associated only with biomass burning. This newly recognized source of tar brC motivates the identification and quantification of tar particulates in other environments affected by ship emissions, and necessitates a refined classification of light-absorbing particulates to avoid misinterpreting their source.
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1 Paul Scherrer Institute, Laboratory of Atmospheric Chemistry, Villigen, Switzerland (GRID:grid.5991.4) (ISNI:0000 0001 1090 7501); National Research Council Canada, Metrology Research Centre, Ottawa, Canada (GRID:grid.24433.32) (ISNI:0000 0004 0449 7958)
2 University of Rostock, Joint Mass Spectrometry Centre, Chair of Analytical Chemistry, Institute of Chemistry, Rostock, Germany (GRID:grid.10493.3f) (ISNI:0000000121858338); University of Eastern Finland, Kuopio, Finland (GRID:grid.9668.1) (ISNI:0000 0001 0726 2490)
3 University of Genoa, Department of Physics, Genoa, Italy (GRID:grid.5606.5) (ISNI:0000 0001 2151 3065); Sezione di Genova, INFN, Genoa, Italy (GRID:grid.470205.4)
4 University of Genoa, Department of Physics, Genoa, Italy (GRID:grid.5606.5) (ISNI:0000 0001 2151 3065)
5 HICE—Helmholtz Virtual Institute for Complex Molecular Systems in Environmental Health, Rostock, Germany (GRID:grid.5606.5); Helmholtz-Zentrum München, Joint Mass Spectrometry Centre, Cooperation Group Comprehensive Molecular Analytics (CMA), Neuherberg, Germany (GRID:grid.4567.0) (ISNI:0000 0004 0483 2525)
6 National Research Council Canada, Metrology Research Centre, Ottawa, Canada (GRID:grid.24433.32) (ISNI:0000 0004 0449 7958)
7 ETH Zurich, Institute for Atmospheric and Climate Science, Zurich, Switzerland (GRID:grid.5801.c) (ISNI:0000 0001 2156 2780)
8 University of Rostock, Joint Mass Spectrometry Centre, Chair of Analytical Chemistry, Institute of Chemistry, Rostock, Germany (GRID:grid.10493.3f) (ISNI:0000000121858338); Helmholtz-Zentrum München, Joint Mass Spectrometry Centre, Cooperation Group Comprehensive Molecular Analytics (CMA), Neuherberg, Germany (GRID:grid.4567.0) (ISNI:0000 0004 0483 2525)
9 Paul Scherrer Institute, Laboratory of Atmospheric Chemistry, Villigen, Switzerland (GRID:grid.5991.4) (ISNI:0000 0001 1090 7501); Laboratory for Air Pollution and Environmental Technology (Empa), Duebendorf, Switzerland (GRID:grid.5991.4)
10 Paul Scherrer Institute, Laboratory of Atmospheric Chemistry, Villigen, Switzerland (GRID:grid.5991.4) (ISNI:0000 0001 1090 7501)
11 HICE—Helmholtz Virtual Institute for Complex Molecular Systems in Environmental Health, Rostock, Germany (GRID:grid.5991.4); Department of Piston Machines and Internal Combustion Engines, Rostock, Germany (GRID:grid.5991.4)
12 Paul Scherrer Institute, Laboratory of Atmospheric Chemistry, Villigen, Switzerland (GRID:grid.5991.4) (ISNI:0000 0001 1090 7501); Alfred Wegener Institute, Bremerhaven, Germany (GRID:grid.10894.34) (ISNI:0000 0001 1033 7684)
13 University of Rostock, Joint Mass Spectrometry Centre, Chair of Analytical Chemistry, Institute of Chemistry, Rostock, Germany (GRID:grid.10493.3f) (ISNI:0000000121858338); HICE—Helmholtz Virtual Institute for Complex Molecular Systems in Environmental Health, Rostock, Germany (GRID:grid.10493.3f); ETH Zurich, Institute for Atmospheric and Climate Science, Zurich, Switzerland (GRID:grid.5801.c) (ISNI:0000 0001 2156 2780)