File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Comparison of the dehalogenation of dihalomethanes (CH 2XI, where X = Cl, Br, I) following ultraviolet photolysis in aqueous and NaCl saltwater environments

TitleComparison of the dehalogenation of dihalomethanes (CH 2XI, where X = Cl, Br, I) following ultraviolet photolysis in aqueous and NaCl saltwater environments
Authors
Issue Date2005
PublisherAmerican Chemical Society. The Journal's web site is located at http://pubs.acs.org/jpca
Citation
Journal Of Physical Chemistry A, 2005, v. 109 n. 26, p. 5872-5882 How to Cite?
AbstractThe ultraviolet photolysis of low concentrations of CH 2XI (X = Cl, Br, I) were investigated in water and saltwater solutions by photochemistry and picosecond time-resolved resonance Raman spectroscopy. Photolysis in both kinds of solutions formed mostly CH 2(OH) 2 and HI and HX products. However, photolysis of the CH 2XI molecules in saltwater resulted in production of some CH 2XCl products not observed in aqueous solutions without salt present. The appearance of these new products in saltwater solutions is accompanied by a decrease in the amount of CH 2(OH) 2, HI, and HX products compared to photolysis in aqueous solutions without salt present. The possible implications for photolysis of CH 2XI and other polyhalomethanes in seawater and other salt aqueous environments compared to nonsaltwater solvated environments is briefly discussed. © 2005 American Chemical Society.
Persistent Identifierhttp://hdl.handle.net/10722/167940
ISSN
2023 Impact Factor: 2.7
2023 SCImago Journal Rankings: 0.604
ISI Accession Number ID
References

 

DC FieldValueLanguage
dc.contributor.authorDu, Yen_US
dc.contributor.authorGuan, Xen_US
dc.contributor.authorKwok, WMen_US
dc.contributor.authorChu, LMen_US
dc.contributor.authorPhillips, DLen_US
dc.date.accessioned2012-10-08T03:13:10Z-
dc.date.available2012-10-08T03:13:10Z-
dc.date.issued2005en_US
dc.identifier.citationJournal Of Physical Chemistry A, 2005, v. 109 n. 26, p. 5872-5882en_US
dc.identifier.issn1089-5639en_US
dc.identifier.urihttp://hdl.handle.net/10722/167940-
dc.description.abstractThe ultraviolet photolysis of low concentrations of CH 2XI (X = Cl, Br, I) were investigated in water and saltwater solutions by photochemistry and picosecond time-resolved resonance Raman spectroscopy. Photolysis in both kinds of solutions formed mostly CH 2(OH) 2 and HI and HX products. However, photolysis of the CH 2XI molecules in saltwater resulted in production of some CH 2XCl products not observed in aqueous solutions without salt present. The appearance of these new products in saltwater solutions is accompanied by a decrease in the amount of CH 2(OH) 2, HI, and HX products compared to photolysis in aqueous solutions without salt present. The possible implications for photolysis of CH 2XI and other polyhalomethanes in seawater and other salt aqueous environments compared to nonsaltwater solvated environments is briefly discussed. © 2005 American Chemical Society.en_US
dc.languageengen_US
dc.publisherAmerican Chemical Society. The Journal's web site is located at http://pubs.acs.org/jpcaen_US
dc.relation.ispartofJournal of Physical Chemistry Aen_US
dc.titleComparison of the dehalogenation of dihalomethanes (CH 2XI, where X = Cl, Br, I) following ultraviolet photolysis in aqueous and NaCl saltwater environmentsen_US
dc.typeArticleen_US
dc.identifier.emailPhillips, DL:phillips@hku.hken_US
dc.identifier.authorityPhillips, DL=rp00770en_US
dc.description.naturelink_to_subscribed_fulltexten_US
dc.identifier.doi10.1021/jp0504928en_US
dc.identifier.pmid16833922-
dc.identifier.scopuseid_2-s2.0-22344448407en_US
dc.identifier.hkuros117000-
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-22344448407&selection=ref&src=s&origin=recordpageen_US
dc.identifier.volume109en_US
dc.identifier.issue26en_US
dc.identifier.spage5872en_US
dc.identifier.epage5882en_US
dc.identifier.isiWOS:000230225000013-
dc.publisher.placeUnited Statesen_US
dc.identifier.scopusauthoridDu, Y=35310175500en_US
dc.identifier.scopusauthoridGuan, X=8313149700en_US
dc.identifier.scopusauthoridKwok, WM=7103129332en_US
dc.identifier.scopusauthoridChu, LM=8595123000en_US
dc.identifier.scopusauthoridPhillips, DL=7404519365en_US
dc.identifier.issnl1089-5639-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats