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Vacuum UV radiation

The correlation is not perfect, but the limitations do not seriously detract from the usefulness of the method. The technique is not limited to vacuum UV radiation. Higher energy radiation can also be used. [Pg.26]

Ito, T. Saito, M. Degradation of oligonucleotides by vacuum-UV radiation in solid roles of the phosphate group and bases, ([published erratum appears in Photochem. Photobiol. 1989 Jun 49(6) 845]) Photochem. Photobiol. 1988, 48 (5), 567-572. [Pg.486]

Takakura, K. Ishikawa, M. Hieda, K. Kobayashi, K. Ito, A. Ito, T. Single-strand breaks in supercoiled DNA induced by vacuum-UV radiation in aqueous solution. Photochem. Photobiol. 1986, 44 (3), 397-400. [Pg.487]

When X-rays are used rather than vacuum UV radiation, electrons are emitted from inner orbitals, and the spectrum obtained reflects this. These spectra also give much scope as an analytical technique. [Pg.16]

Vinogradov, I.P. and Vilesov, F.I. (1976). Luminescence of the OH(j42E+) radical during photolysis of water vapor by vacuum uv radiation, Opt. Spectrosc. 40, 32-34. [Pg.409]

Fozza A, Roch J, Klemberg-Sapieha JE, Kruse A, Hollander A, and Wertheimer MR. Oxidation and ablation of polymers by vacuum-UV radiation from low pressure plasmas. Polym. Prepr. 1997 38 1097. [Pg.59]

Proceedings of the Conference on Vacuum UV Radiation Physics, (Tokyo), Nakai, Y., ed.. Physics Society of Japan, Tokyo. 116 Schafer, T. P. See Siska, P. E. [Pg.297]

Breysse, M., B. Claudel, L. Faure and M. Guenin, 1978, Chemiluminescence induced by Catalysis, in The Rare Earths in Modem Science and Technology, eds. GJ. McCarthy and J.J. Rhyne (Plenum, New York) p. 99. Brousseau, B., F. Frandon, C. Colliex, P. Trebbia and M. Gasgnier, 1974, Energy Loss Spectra and Optical Constants of Rare Earth Metals, Hydrides and Oxides between 5 and 200 eV, in Vacuum UV Radiation Physics, eds. E. Koch, R. Haensel and C. Kunz (Per-gamon-Vieweg, Braunschweig) p. 622. Brundle, C.R. and A.D. Baker eds., 1978, Electron Spectroscopy Theory, Techniques and Applications, Vol. 2 (Academic Press, London). [Pg.315]

The cation is more reactive than the free radical, thereby dominating the initiation reaction. Radical cations can also he formed by high energy electrons, vacuum UV radiation, high intensity electric fields, or anodic oxidation of the monomer. Nuclear chemical initiation involves the use of tritium this method produced very high molecular weight polyisobutylenes and polystyrenes (65). [Pg.934]

Brousseau-Lahaye, B., F. Frandon, C. Colliex, P. Trebbia and M. Casgnier, 1974, Energy loss spectra and optical constants of rare earth metals, hydrides and oxides between 5 and 200 eV, in Vacuum UV Radiation Physics, eds E. [Pg.595]

P, Rabe, K, Radler and H. W. Wolff, in Vacuum UV Radiation Physics, edited by E, Koch et, al, (Vieweg Pergamon, Berlin, 1974),... [Pg.354]


See other pages where Vacuum UV radiation is mentioned: [Pg.225]    [Pg.486]    [Pg.11]    [Pg.461]    [Pg.163]    [Pg.1974]    [Pg.12]    [Pg.685]    [Pg.279]    [Pg.317]    [Pg.489]    [Pg.55]    [Pg.237]    [Pg.682]    [Pg.118]    [Pg.357]    [Pg.113]    [Pg.191]    [Pg.692]    [Pg.162]    [Pg.1090]   


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