Related Experiment Video
Updated: Jan 9, 2026

Analyzing the Photo-oxidation of 2-propanol at Indoor Air Level Concentrations Using Field Asymmetric Ion Mobility Spectrometry
Published on: June 14, 2018
Photoabsorption and Photoionization of Acetaldehyde in the 10.8-21.4 eV Range
Milton M Fujimoto1, Bruno Credidio2, Manoel G P Homem3
1Departamento de Física, Universidade Federal do Paraná, 81531-980 Curitiba, Paraná, Brazil.
Abstract:
An experimental and theoretical investigation of acetaldehyde's photoabsorption and photoionization in the vacuum-ultraviolet energy range is presented. The absorption cross sections and the ionization efficiency were measured using a double-ion-chamber spectrometer in the 10.8-21.4 eV and 13.5-21.4 eV ranges, respectively. No previous reports of these quantities were found in the literature in this energy range. Photoionization and neutral-decay cross sections were derived from these results. Theoretical calculations were performed using the Padé approximant technique and the single-center partial-wave expansion method, which were applied to solve the Lippmann-Schwinger equation to obtain the asymmetry parameters and the photoionization cross sections for the seven outermost valence orbitals. The calculations were performed in the energy range from near-threshold to 35 eV at static-exchange and static-exchange-polarization levels of approximation. Our results are contextualized with recent studies on dissociative photoionization channels and high-resolution photoelectron spectra, enabling correlations with ionic fragmentation pathways. Our experimental and theoretical results were compared between each other and with previous results from the literature, exhibiting good agreement with the available data and providing a comprehensive data set essential for modeling photochemical processes in atmospheric and astrophysical environments.
More Related Videos
Related Concept Videos
IR and UV–Vis Spectroscopy of Aldehydes and Ketones
IR and UV–Vis Spectroscopy of Carboxylic Acids
However, the stretching absorptions for the C=O bond vary depending on the structure of carboxylic acids. The C=O bond of the free carboxylic acids shows a higher stretching frequency, 1760 cm−1, while H-bonded carboxylic acids (dimers) exhibit stretching absorptions at a lower frequency,...
Molecular Spectroscopy: Absorption and Emission
UV–Vis Spectroscopy: Molecular Electronic Transitions
NMR Spectroscopy and Mass Spectrometry of Aldehydes and Ketones
Mass Spectrometry: Aldehyde and Ketone Fragmentation

