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American Institute of Physics

Fig. IV-13. Example of a p-polarized reflection spectrum from Ref. [154] for a stearyl alcohol monolayer on water. The dashed line is the baseline to be subtracted from the spectra. [Reprinted with permission from Joseph T. Buontempo and Stuart A. Rice, J. Chem. Phys. 98(7), 5835-5846 (April 1, 1993). Copyright 1993, American Institute of Physics.]... Fig. IV-13. Example of a p-polarized reflection spectrum from Ref. [154] for a stearyl alcohol monolayer on water. The dashed line is the baseline to be subtracted from the spectra. [Reprinted with permission from Joseph T. Buontempo and Stuart A. Rice, J. Chem. Phys. 98(7), 5835-5846 (April 1, 1993). Copyright 1993, American Institute of Physics.]...
Fig. XVn-16. Infrared absorption spectra of H2 physisorbed on NaCl(lOO) at 30 K. See text for explanations. (From Ref. 96. Reprinted with permission from American Institute of Physics, copyright 1993.)... Fig. XVn-16. Infrared absorption spectra of H2 physisorbed on NaCl(lOO) at 30 K. See text for explanations. (From Ref. 96. Reprinted with permission from American Institute of Physics, copyright 1993.)...
Pratt L R and Hummer G (eds) 1999 Simulation and theory of electrostatic interactions in solution computational chemistry, biophysics and aqueous solutions AlP Conf. Proc. (Sante Fe, NM, 1999) vol 492 (New York American Institute of Physics)... [Pg.558]

Figure A2.5.23. Reduced temperature = T/T versus reduced density p. = p/p for Ne, Ar, Kr, Xe, N2, O2, CO, and CH. The frill curve is the cubic equation (A2.5.26). Reproduced from [10], p 257 by pennission of the American Institute of Physics. Figure A2.5.23. Reduced temperature = T/T versus reduced density p. = p/p for Ne, Ar, Kr, Xe, N2, O2, CO, and CH. The frill curve is the cubic equation (A2.5.26). Reproduced from [10], p 257 by pennission of the American Institute of Physics.
Figure A2.5.31. Calculated TIT, 0 2 phase diagram in the vicmity of the tricritical point for binary mixtures of ethane n = 2) witii a higher hydrocarbon of contmuous n. The system is in a sealed tube at fixed tricritical density and composition. The tricritical point is at the confluence of the four lines. Because of the fixing of the density and the composition, the system does not pass tiirough critical end points if the critical end-point lines were shown, the three-phase region would be larger. An experiment increasing the temperature in a closed tube would be represented by a vertical line on this diagram. Reproduced from [40], figure 8, by pennission of the American Institute of Physics. Figure A2.5.31. Calculated TIT, 0 2 phase diagram in the vicmity of the tricritical point for binary mixtures of ethane n = 2) witii a higher hydrocarbon of contmuous n. The system is in a sealed tube at fixed tricritical density and composition. The tricritical point is at the confluence of the four lines. Because of the fixing of the density and the composition, the system does not pass tiirough critical end points if the critical end-point lines were shown, the three-phase region would be larger. An experiment increasing the temperature in a closed tube would be represented by a vertical line on this diagram. Reproduced from [40], figure 8, by pennission of the American Institute of Physics.
Kestin J (ed) 1973 Transport Phenomena, AlP Conference Proceedings No. 11 (New York American institute of Physics)... [Pg.691]

Figure A3.14.il. Spiral waves imaged by photoelectron electron microscopy for the oxidation of CO by O2 on a Pt(l 10) single crystal under UHV conditions. (Reprinted with pennission from [35], The American Institute of Physics.)... Figure A3.14.il. Spiral waves imaged by photoelectron electron microscopy for the oxidation of CO by O2 on a Pt(l 10) single crystal under UHV conditions. (Reprinted with pennission from [35], The American Institute of Physics.)...
Figure Bl.7.13. A schematic diagram of an ion-guide mass spectrometer. (Ervin K M and Annentrout P B 1985 Translational energy dependence of Ar + XY —> ArX + Y from thennal to 30 eV c.m. J. Chem. Phys. 83 166-89. Copyright American Institute of Physics Publishing. Reproduced with pemiission.)... Figure Bl.7.13. A schematic diagram of an ion-guide mass spectrometer. (Ervin K M and Annentrout P B 1985 Translational energy dependence of Ar + XY —> ArX + Y from thennal to 30 eV c.m. J. Chem. Phys. 83 166-89. Copyright American Institute of Physics Publishing. Reproduced with pemiission.)...
Bertini I, Martini G and Luchinat C 1994 Relaxation, background, and t neory Handbook of Electron Spin Resonance (ed C Poole and H Farach (New York American Institute of Physics) oh 3, pp 51-77... [Pg.1588]

Burke P G 1996 Atomic, Molecular and Optical Physics Handbook ed G W Drake (New York American Institute of Physics Press) oh 45... [Pg.2058]

Dynamics and Pattern Formation in Biological and Complex Systems ed S Kim, K J Lee and W Sung (Melville, NY American Institute of Physics) pp 95-111... [Pg.2665]

Bruno G, Capezuttuto P and Losurdo M 1995 On the use of the piasma in iii-V semiconductor processing Phenomena In Ionized Gases (ICPIG Hoboken, NJ, 1995 (AiP Conference Proceedings voi 22) ed K FI Becker, W E Carr and E E Kunhardt (Woodbury, NY American Institute of Physics) pp 146-55... [Pg.2812]

References D. D. Wagman, et ah, The NBS Tables of Chemical Thermodynamic Properties, in J. Phys. Chem. Ref. Data, 11 2,1982 M. W. Chase, et ah, JANAF Thermochemical Tables, 3rd ed., American Chemical Society and the American Institute of Physics, 1986 (supplements to JANAF appear in J. Phys. Chem. Ref. Data) Thermodynamic Research Center, TRC Thermodynamic Tables, Texas A M University, College Station, Texas I. Barin and O. Knacke, Thermochemical Properties of Inorganic Substances, Springer-Verlag, Berlin, 1973 J. B. Pedley, R. D. Naylor, and S. P. Kirby, Thermochemical Data of Organic Compounds, 2nd ed.. Chapman and Hall, London, 1986 V. Majer and V. Svoboda, Enthalpies of Vaporization of Organic Compounds, International Union of Pure and Applied Chemistry, Chemical Data Series No. 32, Blackwell, Oxford, 1985. [Pg.533]

C. E. Poole, Jr. and H. A. Earach, eds.. Handbook of Electron Spin Resonance Datasources, Computer Technology, Relaxation and ENDOR, American Institute of Physics, New York, 1994. [Pg.410]

N. J. Eisch, ed.. Advances in Plasma Physics Proceedings of the Thomas H. Stix Symposium, American Institute of Physics, AIP Press, Woodbury, N. Y., 1994. [Pg.120]

JxTNxTF Thermochemical Tables, 3rd ed., American Chemical Society, Washington, D.C., and American Institute of Physics, New York, for the National Bureau of Standards, 1985. [Pg.149]

R. A. Matula,/. PIjs. Chem. Ref. Data 8, 4 (1979). American Institute of Physics resistivity tables. [Pg.87]

It should be noted that the values for 100 percent do not agree with some data avadahle elsewhere, e.g., American Institute of Physics Handbook, McGraw-HiU, New York, 1957. Also, see Atack, Handbook of Chemical Data, Reinhold, New York, 1957. [Pg.155]

Bauer, F. (1982), Behavior of Ferroelectric Ceramics and PVF2 Polymers Under Shock Loading, in Shock Waves in Condensed Matter—1981 (edited by W.J. Nellis, L. Seaman, and R.A. Graham) American Institute of Physics, New York, pp. 251-267. [Pg.70]

Brown, L.M., Pais, A. and Pippard, B. (1995) Twentieth Century Physics, 3 volumes (Institute of Physics Publishing and American Institute of Physics, Bristol. Philadelphia and New York). [Pg.148]

Mulvey, T. (1995) Electron-beam instruments, in 20th Century Physics, vol. 3, ed. Pais, A. et id. (Institute of Physics Publishing, and New York American Institute of Physics Press, Bristol and Philadelphia) p. 1565. [Pg.248]

Information about this splendid compilation came to me from a chemist, Robert Weast (1985), who was editor from 1952 until 1988... 37 years He also informed me that the creation (jointly by the American Chemical Society and the American Institute of Physics) of the Journal of Physical and Chemical Reference Data, which began publication in 1972, was encouraged by the results of a survey which indicated how widely the Rubber Bible was used. Weast describes this journal as a truly outstanding source of critically evaluated data . In saying this, he underlined the crucial role of editors and contributors critical judgment in selecting data for such compilations. David Tide, the editor of the journal, in 1989 succeeded Robert... [Pg.493]

Fig. 12.2. EPR spectra of small organic free radicals, (a) Spectrum of the benzene radical anion. [From J. R. Bolton, Mol. Phys. 6 219 (1963). Reproduced by permission of Taylor and Francis, Ltd.] (b) Spectrum of the ethyl radical. [From R. W. Fessenden and R. H. Schuler, J. Chem. Phys. 33 935 (1960) J. Chem. Phys. 39 2147 (1963). Reproduced by permission of the American Institute of Physics.]... Fig. 12.2. EPR spectra of small organic free radicals, (a) Spectrum of the benzene radical anion. [From J. R. Bolton, Mol. Phys. 6 219 (1963). Reproduced by permission of Taylor and Francis, Ltd.] (b) Spectrum of the ethyl radical. [From R. W. Fessenden and R. H. Schuler, J. Chem. Phys. 33 935 (1960) J. Chem. Phys. 39 2147 (1963). Reproduced by permission of the American Institute of Physics.]...
Fig. 13.11. A schematic drawing of the potential energy surfaces for the photochemical reactions of stilbene. Approximate branching ratios and quantum yields for the important processes are indicated. In this figure, the ground- and excited-state barrier heights are drawn to scale representing the best available values, as are the relative energies of the ground states of Z- and E -stilbene 4a,4b-dihydrophenanthrene (DHP). [Reproduced from R. J. Sension, S. T. Repinec, A. Z. Szarka, and R. M. Hochstrasser, J. Chem. Phys. 98 6291 (1993) by permission of the American Institute of Physics.]... Fig. 13.11. A schematic drawing of the potential energy surfaces for the photochemical reactions of stilbene. Approximate branching ratios and quantum yields for the important processes are indicated. In this figure, the ground- and excited-state barrier heights are drawn to scale representing the best available values, as are the relative energies of the ground states of Z- and E -stilbene 4a,4b-dihydrophenanthrene (DHP). [Reproduced from R. J. Sension, S. T. Repinec, A. Z. Szarka, and R. M. Hochstrasser, J. Chem. Phys. 98 6291 (1993) by permission of the American Institute of Physics.]...

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