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Transforms frequency shift

It is also the same for Laplace transform. Frequency Shifting For any real frequency ujq,... [Pg.76]

Figure 12.12 Kinetics of the (2 x 2) —3CO - ( /l9 xvT9)R23.4° — 13CO phase transition on a Pt( 111) electrode in a CO-saturated 0.1M H2SO4 electrolyte, observed via SFG of atop CO. The frequency shift data in (b) and (e) indicate that a new potential is estabhshed on the electrode within 0.2 s. The forward transformation is much slower than the reverse. There are minimal differences between the first and second cycles, indicating minimal change in electrolyte composition during kinetic measurements. Figure 12.12 Kinetics of the (2 x 2) —3CO - ( /l9 xvT9)R23.4° — 13CO phase transition on a Pt( 111) electrode in a CO-saturated 0.1M H2SO4 electrolyte, observed via SFG of atop CO. The frequency shift data in (b) and (e) indicate that a new potential is estabhshed on the electrode within 0.2 s. The forward transformation is much slower than the reverse. There are minimal differences between the first and second cycles, indicating minimal change in electrolyte composition during kinetic measurements.
Larger frequency shifts lead to more sensitive structural discriminations. In the IR, the (i-shcct amide I is distinctively lower in frequency than other structural types, particularly for aggregates, a form often seen in unfolding experiments. However, owing to the high signal-to-noise ratio (S/N) of Fourier transform IR (FTIR), one can detect components having smaller frequency separations. This effective resolution... [Pg.136]

Subtractively normalized interfacial Fourier transform infrared spectroscopy (SNIFTIRS), has been used extensively to examine interactions of species at the electrode/electrolyte interface. In the present work, the method has been extended to probe interactions at the mercury solution interface. The diminished potential dependent frequency shifts of species adsorbed at mercury electrodes are compared with shifts observed for similar species adsorbed at d-band metals. [Pg.338]

The anharmonicities of the potential contribute by the terms involving the constants x, g, y,. .. as well as the energy shifts AEx = 0(h2),. .. and the frequency shifts Aw, = 0(h2),. These anharmonic constants can be calculated by the Van Vleck contact transformations [20] as well as by a semi-classical method based on an h expansion around the equilibrium point [14], which confirms that the Dunham expansion (2.8) is a series in powers of h. Systematic methods have been developed to carry out the Van Vleck contact transformations, as in the algebraic quantization technique by Ezra and Fried [21]. It should be noted that the constants x and g can also be obtained from the classical-mechanical Birkhoff normal forms [22], The energy shifts AEx,... [Pg.497]

The time-like part of the gauge transform gives the frequency shift [44] ... [Pg.83]

We describe the Zak-Gabor transform for a single stripe and a chosen fixed scale parameter D. Let M be a number of translations of g, and K be the number of frequency shifts where we always take M = P/K. The Gabor elementary functions (GEF), are defined as shifted and modulated versions of g, namely... [Pg.266]

Varian VXR 500 NMR spectrometer operating at a proton frequency of 500 MHz. The spectral width was 6000 Hz with the carrier frequency at the HDO resonance. The solvent resonance was suppressed by presaturation. Each FID was composed of 16 k data points with 80 transients. The delay between successive transients was 2.8 s. The time domain data were processed by zero-filling to 32 k points, exponential multiplication (0.5 Hz) and Fourier transformation. Chemical shifts were referenced to internal sodium 3-(trimethylsilyl)-propionate-2,2,3,3-d4. The Kj values were obtained by nonlinear least square fit of the data to the equation... [Pg.681]


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See also in sourсe #XX -- [ Pg.286 ]

See also in sourсe #XX -- [ Pg.286 ]




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Frequency shifts

Frequency transformation

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