Raman Spectra of Hydrogen Peroxide in Condensed Phases. I. The Spectra of the Pure Liquid and Its Aqueous Solutions
dc.contributor.author | Taylor, Robert Cooper | en_US |
dc.contributor.author | Cross, Paul C. | en_US |
dc.date.accessioned | 2010-05-06T22:34:01Z | |
dc.date.available | 2010-05-06T22:34:01Z | |
dc.date.issued | 1956-01 | en_US |
dc.identifier.citation | Taylor, 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.uri | https://hdl.handle.net/2027.42/70695 | |
dc.description.abstract | The 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.extent | 3102 bytes | |
dc.format.extent | 297761 bytes | |
dc.format.mimetype | text/plain | |
dc.format.mimetype | application/pdf | |
dc.publisher | The American Institute of Physics | en_US |
dc.rights | © The American Institute of Physics | en_US |
dc.title | Raman Spectra of Hydrogen Peroxide in Condensed Phases. I. The Spectra of the Pure Liquid and Its Aqueous Solutions | en_US |
dc.type | Article | en_US |
dc.subject.hlbsecondlevel | Physics | en_US |
dc.subject.hlbtoplevel | Science | en_US |
dc.description.peerreviewed | Peer Reviewed | en_US |
dc.contributor.affiliationum | Department of Chemistry, University of Michigan, Ann Arbor, Michigan | en_US |
dc.contributor.affiliationother | Department of Chemistry, University of Washington, Seattle, Washington | en_US |
dc.description.bitstreamurl | http://deepblue.lib.umich.edu/bitstream/2027.42/70695/2/JCPSA6-24-1-41-1.pdf | |
dc.identifier.doi | 10.1063/1.1700850 | en_US |
dc.identifier.source | The Journal of Chemical Physics | en_US |
dc.identifier.citedreference | P. A. Giguere, J. Chem. Phys. 18, 88 (1950). | en_US |
dc.identifier.citedreference | R. C. Taylor, J. Chem. Phys. 18, 898 (1950). | en_US |
dc.identifier.citedreference | O. Bain and P. A. Giguere, Can. J. Chem. 33, 527 (1955). | en_US |
dc.identifier.citedreference | A. Simon and F. Feher, Z. Elektrochem. 41, 290 (1935). | en_US |
dc.identifier.citedreference | F. Feher, Ber. Deut. Chem. Ges. 72B, 1778 (1939). | en_US |
dc.identifier.citedreference | J. H. Hibben, J. Chem. Phys. 5, 166 (1937). | en_US |
dc.identifier.citedreference | Cross, Burnham, and Leighton, J. Am. Chem. Soc. 59, 1134 (1937). | en_US |
dc.identifier.citedreference | P. M. Gross, Jr. and R. C. Taylor, J. Am. Chem. Soc. 72, 2075 (1950). | en_US |
dc.identifier.citedreference | F. Feher, Ber. Deut. Chem. Ges. 72, 1789 (1939). | en_US |
dc.identifier.citedreference | R. C. Taylor (unpublished work). | en_US |
dc.identifier.citedreference | See, 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.citedreference | W. T. Foley and P. A. Giguere, Can. J. Chem. 29, 123 (1951). | en_US |
dc.identifier.citedreference | A. G. Mitchell and W. F. K. Wynne‐Jones, Discussions Faraday Soc. No. 15, 161 (1953). | en_US |
dc.owningcollname | Physics, Department of |
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