Conversion of oxygenated and hydrocarbon molecules to particulate matter using stable isotopes as tracers

Abstract

Fuels are continuing to be derived from fossil sources, but as production technology improves, biofuels and synthetic fuels are expected to emerge as scalable long-term sources of liquid fuels. Efforts are being made to ensure that this next-generation of fuels is cleaner burning than the last. In order to inform the production and processing of cleaner burning fuels, more needs to be known about how molecular structure influences the formation of pollutant emissions. Reducing airborne quantities of particulate matter (PM) is of particular interest for human health and the environment. This publication presents a 13 C labelling technique, which has been developed and applied to identify the influence of local molecular structure on the formation of PM. The paper applied the technique based on the 13 C stable isotope to trace the conversion of individual carbon atoms to PM in the case of several oxygenated and hydrocarbon molecules. A laminar tube reactor facility has been used for generating and collecting samples of PM under pyrolysis conditions. A number of single-component oxygenated and hydrocarbons (ethanol, propanol, pentanol, cyclopentanol, ethyl acetate, and toluene) have been enriched with 13 C at specific carbon atom locations and the 13 C/ 12 C isotope ratios of PM were measured. The contribution to PM of particular carbon atoms within a molecule was evaluated, and the results shed new light of how individual carbon atoms in a molecule convert to PM. It was found that the conversion to PM of different atoms within a molecule varies widely, depending on the identity of their neighbouring moiety. Furthermore, it was shown that oxygen-containing functional groups have a significant influence on the formation of particulates, partly through a reduction in the conversion to PM of carbon atoms, which are adjacent to oxygen atoms.