Kinetic studies of the deactivation of O 2 ( 1 Σ g + ) and O( 1 D)
dc.contributor.author | Shi, Jichun | en_US |
dc.contributor.author | Barker, John R. | en_US |
dc.date.accessioned | 2006-04-28T16:58:23Z | |
dc.date.available | 2006-04-28T16:58:23Z | |
dc.date.issued | 1990-12 | en_US |
dc.identifier.citation | Shi, Jichun; Barker, John R. (1990)."Kinetic studies of the deactivation of O 2 ( 1 Σ g + ) and O( 1 D)." International Journal of Chemical Kinetics 22(12): 1283-1301. <http://hdl.handle.net/2027.42/38441> | en_US |
dc.identifier.issn | 0538-8066 | en_US |
dc.identifier.issn | 1097-4601 | en_US |
dc.identifier.uri | https://hdl.handle.net/2027.42/38441 | |
dc.description.abstract | The kinetics of the deactivation of O 2 ( 1 Σ g + ) is studied in real time. O 2 ( 1 Σ g + ) is generated in this system by the O( 1 D) + O 2 reaction following O 3 laser flash photolysis in the presence of excess O 2 , and it is monitored by its characteristic emission band at 762 nm. Quenching rate constants were obtained for O 2 , O 3 , N 2 , CO 2 , H 2 O, CF 4 and the rare gases. Since O( 1 D) is the precursor for the formation of O 2 ( 1 Σ g + ), the addition of an O( 1 D) quencher effectively lowers the initial concentration of O 2 ( 1 Σ g + ). By measuring the initial intensity of the 762 nm fluorescence signal, the relative quenching efficiencies were determined for O( 1 D) quenching by N 2 , CO 2 , Xe, and Kr with respect to O 2 ; the results are in good agreement with literature values. | en_US |
dc.format.extent | 864659 bytes | |
dc.format.extent | 3118 bytes | |
dc.format.mimetype | application/pdf | |
dc.format.mimetype | text/plain | |
dc.language.iso | en_US | |
dc.publisher | John Wiley & Sons, Inc. | en_US |
dc.subject.other | Chemistry | en_US |
dc.subject.other | Physical Chemistry | en_US |
dc.title | Kinetic studies of the deactivation of O 2 ( 1 Σ g + ) and O( 1 D) | en_US |
dc.type | Article | en_US |
dc.rights.robots | IndexNoFollow | en_US |
dc.subject.hlbsecondlevel | Biological Chemistry | en_US |
dc.subject.hlbsecondlevel | Chemical Engineering | en_US |
dc.subject.hlbsecondlevel | Chemistry | en_US |
dc.subject.hlbsecondlevel | Materials Science and Engineering | en_US |
dc.subject.hlbtoplevel | Health Sciences | en_US |
dc.subject.hlbtoplevel | Science | en_US |
dc.subject.hlbtoplevel | Engineering | en_US |
dc.description.peerreviewed | Peer Reviewed | en_US |
dc.contributor.affiliationum | Department of Atmospheric, Oceanic and Space Sciences, Space Physics Research Laboratory, The University of Michigan, Ann Arbor, Michigan 48109-2143 | en_US |
dc.contributor.affiliationum | Department of Atmospheric, Oceanic and Space Sciences, Space Physics Research Laboratory, The University of Michigan, Ann Arbor, Michigan 48109-2143 | en_US |
dc.description.bitstreamurl | http://deepblue.lib.umich.edu/bitstream/2027.42/38441/1/550221207_ftp.pdf | en_US |
dc.identifier.doi | http://dx.doi.org/10.1002/kin.550221207 | en_US |
dc.identifier.source | International Journal of Chemical Kinetics | en_US |
dc.owningcollname | Interdisciplinary and Peer-Reviewed |
Files in this item
Remediation of Harmful Language
The University of Michigan Library aims to describe library materials in a way that respects the people and communities who create, use, and are represented in our collections. Report harmful or offensive language in catalog records, finding aids, or elsewhere in our collections anonymously through our metadata feedback form. More information at Remediation of Harmful Language.
Accessibility
If you are unable to use this file in its current format, please select the Contact Us link and we can modify it to make it more accessible to you.