Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Louis J. Schoen"'
Publikováno v:
Journal of Applied Physics. 21:44-48
High velocity flames in half‐open tubes produced by placing a grid augmenter in the path of an advancing flame are described. High speed schlieren motion pictures and instantaneous pressure measurements are used to study flame structure and accompa
Publikováno v:
Journal of the American Chemical Society. 83:4131-4134
Autor:
Louis J. Schoen
Publikováno v:
The Journal of Chemical Physics. 45:2773-2776
Flash photolysis combined with matrix‐isolation spectroscopy has been employed to investigate the decomposition of a cyanogen azide—nitrogen solid at 20.4°K. Two primary processes have been observed leading to the formation of NCN radicals eithe
Publikováno v:
Symposium on Combustion and Flame, and Explosion Phenomena. 3:168-176
Publikováno v:
Journal of the American Chemical Society. 78:47-49
Publikováno v:
Journal of the American Chemical Society. 78:50-52
Publikováno v:
The Journal of Chemical Physics. 38:461-463
The infrared spectrum of gaseous difluoramine, NF2H, has been investigated over the range 250–4000 cm—1. Four bands of NF2D have also been observed. The fundamental frequencies (in cm—1) and their species are as follows: NF2H:ν1(a′):3193;ν2
Autor:
Louis J. Schoen, Ralph Klein
Publikováno v:
The Journal of Chemical Physics. 24:1094-1096
Observations on the photodecomposition of mixtures of normal and deuterated formaldehydes give reliable data for calculating the stability of the HCO radical. The relative occurrence of the intramolecular split and the H‐atom dissociation reaction
Publikováno v:
The Journal of Chemical Physics. 30:58-60
The activation energies and steric factors of the abstraction reactions D+D2CO→D2+DCO and D+CH4→HD+CH3 have been determined by the technique of competing reactions. Mixtures of formaldehyde‐d2 and H2 as well as formaldehyde‐d2 and methane wer
Publikováno v:
The Journal of Chemical Physics. 48:1534-1536
Infrared absorption in the region of 3450 cm−1 has been observed in water–rare‐gas matrices subjected to vacuum‐ultraviolet photolysis at 20.4° and 4.2°K. The splittings and isotope frequency ratios obtained from H216O–D216O, H216O–H218