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Isomer-Selective Generation and Spectroscopic Characterization of Biofuel Intermediates

Online combustion analysis relies heavily on spectral data to detect reactive intermediates isomer-selectively to establish e.g. kinetic flame models. Due to the difficulty to generate these species cleanly, spectral data are rather scarce. Here we report on the selective generation of three picolyl radical isomers (C5H4N-CH2*) by deamination of aminomethylpyridines. Picolyl radicals are relevant in biofuel combustion, and could now be characterized by threshold photoelectron spectroscopy using synchrotron radiation. Vibrationally resolved bands and distinct ionization energies allow for isomer-specific detection of these elusive species in complex environments and permit us to explore new avenues in soot- and NOx formation kinetics.

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Combustion reactions followed by PEPICO (CRF-PEPICO) ion rastering setup. The suppression of false coincidences opens up new analytical applications.

Breaking Through the False Coincidence Barrier in Electron–Ion Coincidence Experiments

The false coincidence background has so far limited the analytical application of PEPICO, photoelectron photoion coincidence. A new photoioin rastering technique has been developed to separate the wheat from the chaff and identify true coincidences based on the ion hit time and position. This expands the dynamic range of the experiment by at least two orders of magnitude, allowing for novel applications to look for reactive intermediates and short lived species in reaction environments.

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