The measurement of Polycyclic Aromatic Hydrocarbons (PAHs) in flames is essential for the understanding of soot formation. In comparison to conventional aromatics-sampling techniques, a new technique was proposed that involves fewer manual operations and no hazardous extraction solvents. Apparatus and experimental procedures of the newly proposed adsorptive-sampling and desorptive-extraction technique for aromatic-hydrocarbon measurements were established in this study. The capabilities and limitations of this new technique were assessed in terms of limits of detection, sampling locations and data repeatability. The accuracy of this technique was also evaluated. Aromatic-hydrocarbon species concentrations were measured in laminar co-flow diffusion flames of ethylene (C2H4) and synthetic paraffinic kerosene (SPK). The results obtained from the ethylene flame were compared to its numerical simulation, with the goal of achieving agreement within an order of magnitude. The differences between simulated values and experimental measurements, along with the limitations of the technique, were used as an indication of the accuracy of the technique.

The measurement of Polycyclic Aromatic Hydrocarbons (PAHs) in flames is essential for the understanding of soot formation. In comparison to conventional aromatics-sampling techniques, a new technique was proposed that involves fewer manual operations and no hazardous extraction solvents. Apparatus and experimental procedures of the newly proposed adsorptive-sampling and desorptive-extraction technique for aromatic-hydrocarbon measurements were established in this study. The capabilities and limitations of this new technique were assessed in terms of limits of detection, sampling locations and data repeatability. The accuracy of this technique was also evaluated. Aromatic-hydrocarbon species concentrations were measured in laminar co-flow diffusion flames of ethylene (C2H4) and synthetic paraffinic kerosene (SPK). The results obtained from the ethylene flame were compared to its numerical simulation, with the goal of achieving agreement within an order of magnitude. The differences between simulated values and experimental measurements, along with the limitations of the technique, were used as an indication of the accuracy of the technique.