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Raman Spectra of Hydrogen Peroxide in Condensed Phases. I. The Spectra of the Pure Liquid and Its Aqueous Solutions

dc.contributor.authorTaylor, Robert Cooperen_US
dc.contributor.authorCross, Paul C.en_US
dc.date.accessioned2010-05-06T22:34:01Z
dc.date.available2010-05-06T22:34:01Z
dc.date.issued1956-01en_US
dc.identifier.citationTaylor, Robert C.; Cross, Paul C. (1956). "Raman Spectra of Hydrogen Peroxide in Condensed Phases. I. The Spectra of the Pure Liquid and Its Aqueous Solutions." The Journal of Chemical Physics 24(1): 41-44. <http://hdl.handle.net/2027.42/70695>en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/70695
dc.description.abstractThe Raman spectrum of liquid 99.5% H2O2 has been obtained at 30° and −40°C and compared with the spectrum of 90% D2O2 at −40°C. Three bands not previously reported were observed and their assignment, together with that of the remaining bands, is discussed.Raman spectra were also obtained for aqueous solutions at 30° and −40°C over the complete concentration range. The interpretation is qualitatively in agreement with the results of other work which indicate that the addition of hydrogen peroxide to water results in more extensive hydrogen bonding and an increased degree of order in the solutions.en_US
dc.format.extent3102 bytes
dc.format.extent297761 bytes
dc.format.mimetypetext/plain
dc.format.mimetypeapplication/pdf
dc.publisherThe American Institute of Physicsen_US
dc.rights© The American Institute of Physicsen_US
dc.titleRaman Spectra of Hydrogen Peroxide in Condensed Phases. I. The Spectra of the Pure Liquid and Its Aqueous Solutionsen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelPhysicsen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Chemistry, University of Michigan, Ann Arbor, Michiganen_US
dc.contributor.affiliationotherDepartment of Chemistry, University of Washington, Seattle, Washingtonen_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/70695/2/JCPSA6-24-1-41-1.pdf
dc.identifier.doi10.1063/1.1700850en_US
dc.identifier.sourceThe Journal of Chemical Physicsen_US
dc.identifier.citedreferenceP. A. Giguere, J. Chem. Phys. 18, 88 (1950).en_US
dc.identifier.citedreferenceR. C. Taylor, J. Chem. Phys. 18, 898 (1950).en_US
dc.identifier.citedreferenceO. Bain and P. A. Giguere, Can. J. Chem. 33, 527 (1955).en_US
dc.identifier.citedreferenceA. Simon and F. Feher, Z. Elektrochem. 41, 290 (1935).en_US
dc.identifier.citedreferenceF. Feher, Ber. Deut. Chem. Ges. 72B, 1778 (1939).en_US
dc.identifier.citedreferenceJ. H. Hibben, J. Chem. Phys. 5, 166 (1937).en_US
dc.identifier.citedreferenceCross, Burnham, and Leighton, J. Am. Chem. Soc. 59, 1134 (1937).en_US
dc.identifier.citedreferenceP. M. Gross, Jr. and R. C. Taylor, J. Am. Chem. Soc. 72, 2075 (1950).en_US
dc.identifier.citedreferenceF. Feher, Ber. Deut. Chem. Ges. 72, 1789 (1939).en_US
dc.identifier.citedreferenceR. C. Taylor (unpublished work).en_US
dc.identifier.citedreferenceSee, for example, reference 6 and also: J. Burnham and P. A. Leighton, J. Am. Chem. Soc. 59, 424 (1937); J. Chien, J. Am. Chem. Soc. 69, 20 (1947), and others.en_US
dc.identifier.citedreferenceW. T. Foley and P. A. Giguere, Can. J. Chem. 29, 123 (1951).en_US
dc.identifier.citedreferenceA. G. Mitchell and W. F. K. Wynne‐Jones, Discussions Faraday Soc. No. 15, 161 (1953).en_US
dc.owningcollnamePhysics, Department of


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