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pro vyhledávání: '"Diane P. Hessler"'
Autor:
Diane P. Hessler, Fritz H. Frimmel
Publikováno v:
Aquatic and Surface Photochemistry ISBN: 9781351069847
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6dcb94dae91b640a4c1fc597aefcffe9
https://doi.org/10.1201/9781351069847-10
https://doi.org/10.1201/9781351069847-10
Publikováno v:
Journal of Photochemistry and Photobiology B: Biology. 36:55-60
The quenching of singlet oxygen (O21Δg) by humic substances (HSs) of different origins has been investigated by measurements of the singlet oxygen luminescence at 1270 nm. A Stern—Volmer analysis of the quenching of the emission by HSs shows a str
Publikováno v:
Journal of Photochemistry and Photobiology A: Chemistry. 86:171-176
A number of mixed crystals, prepared by resolidification of a melt containing benzophenones and various hydrogen donors (molar ratio, usually 1:1), were found, on the basis of powder X-ray diffractograms and phase diagrams, to be a mixture of the cry
Publikováno v:
Acta Hydrochimica et Hydrobiologica. 21:209-214
The degradation of two pesticides: atrazine and metazachlor was investigated in aqueous solution under UV-irradiation with and without H2O2. Rate constants of the photochemical degradation were determined applying a first order kinetics and quantum y
Autor:
André M. Braun, Diane P. Hessler, James R. Fehlner, Nicholas J. Turro, Warren Ruderman, Kevin M. Welsh, Dow Firnberg
Publikováno v:
The Journal of Organic Chemistry. 53:3731-3735
The photochlorination of n-alkanes adsorbed on pentasil zeolites proceeds with up to a 20-fold greater selectivity for the monochlorination of terminal methyl groups compared to the selectivity observed when the reaction is carried out in a homogeneo
Autor:
Nicholas J. Turro, James R. Fehlner, Warren Ruderman, Kevin M. Welsh, Dow Firnberg, Diane P. Hessler, André M. Braun
Publikováno v:
ChemInform. 20
The photochlorination of n-alkanes adsorbed on pentasil zeolites proceeds with up to a 20-fold greater selectivity for the monochlorination of terminal methyl groups compared to the selectivity observed when the reaction is carried out in a homogeneo