2002
DOI: 10.1088/0963-0252/11/2/314
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Reactive molecular plasmas

Abstract: Publisher's Note This article was temporarily included in this electronic issue by mistake; it was due to be part of the International Conference on Phenomena in Ionized Gases (ICPIG) special issue which appeared in August 2002. The article was withdrawn from the print version of this issue.

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Cited by 23 publications
(25 citation statements)
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“…Several methods have appeared to measure the O-atom density in highly dissociated oxygen. The methods include optical spectroscopy [12], [13], mass spectrometry [14], [15], gas titration [16], [17], and catalytic probes [18]. The latter was found to have some advantages over other techniques, as catalytic probes enable real/time measurements and do not disturb the original concentration of O atoms.…”
Section: Introductionmentioning
confidence: 99%
“…Several methods have appeared to measure the O-atom density in highly dissociated oxygen. The methods include optical spectroscopy [12], [13], mass spectrometry [14], [15], gas titration [16], [17], and catalytic probes [18]. The latter was found to have some advantages over other techniques, as catalytic probes enable real/time measurements and do not disturb the original concentration of O atoms.…”
Section: Introductionmentioning
confidence: 99%
“…The second part of this statement is in a good agreement with the increase of γ p (Table ) and XPS data discussed further (Table ), while features of the surface etching were determined by the type of electrode (anode or cathode) and initial characteristics of chitosan sample. DC discharge treatment causes separation of the plasma active components (electrons and ions), resulting in different etching processes occurring at the cathode and anode . We assume that plasma modification of chitosan films on the anode led mainly to local destruction of “soft” amorphous regions by plasma electrons, while treatment on the cathode could cause more significant etching by ions.…”
Section: Resultsmentioning
confidence: 99%
“…This emission comes from the NO γ system between 200 and 300 nm and from the NO β system between 300 and 400 nm. The excited NO(B) states from which the UV radiation is produced (transition from NO(B) to NO(X)) are created in the late afterglow region by the long-lived atom species [6,8] :…”
Section: Experimental Setup and Methodsmentioning
confidence: 99%
“…where M again indicates a third body. In this context, the intensity of the NO β system becomes [8,9] :…”
Section: Experimental Setup and Methodsmentioning
confidence: 99%