Abstract

Methane was irradiated with microwave operated helium (21.2 eV) and neon (16.7-16.8 eV) resonance lamps which were separated from the reaction vessel by an aluminum window. The quantum yields of the stable end products have been determined at methane pressures ranging from 1 to 20 torr. Over this pressure range the abundances of the primary ions, determined through various diagnostic experiments, are within experimental error the same at 21.2 eV as at 16.7-16.8 eV ( , ), and are in good agreement with the primary mass spectra obtained in a photoionization mass spectrometer under collision free conditions (P < 10-5 torr). The which is formed by the reaction: loses a proton by an undetermined mechanism to give C2H4 as a product. There is no evidence for the formation of neutral fragments such as H2, C, CH or CH2 at 16.7-16.8 eV. The fact that the ionization quantum is equal to unity in this energy range accounts for the absence of these intermediates. At 21.2 eV where (Φionization = 0.95) there is concrete evidence for the formation of carbon atoms (Φ(C) ⩾ 0.002). In an attempt to demonstrate the usefulness of enclosed neon and helium resonance light sources in the ion-molecule kinetic studies, the relative probabilities of transfer of H- over D- from various partially deuterium labeled hydrocarbons to (or ) has been determined. The results presented in this article resolve the existing disagreements between previous helium resonance photolysis studies on CH4.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.