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Signal homogeneity

The advantages of differential ion acceleration and detection in terms of rf power and signal homogeneity have been elucidated by Dunbar (4). In our cell design, rf voltages of up to 400 Volt (peak-to-peak) can be applied differentially, which allows for rapid acceleration and ejection. [Pg.85]

The liquid was applied and dried on cellulose filter (diameter 25 mm). In the present work as an analytical signal we took the relative intensity of analytical lines. This approach reduces non-homogeneity and inequality of a probe. Influence of filter type and sample mass on features of the procedure was studied. The dependence of analytical lines intensity from probe mass was linear for most of above listed elements except Ca presented in most types of filter paper. The relative intensities (reduced to one of the analysis element) was constant or dependent from mass was weak in determined limits. This fact allows to exclude mass control in sample pretreatment. For Ca this dependence was non-linear, therefore, it is necessary to correct analytical signal. Analysis of thin layer is characterized by minimal influence of elements hence, the relative intensity explicitly determines the relative concentration. As reference sample we used solid synthetic samples with unlimited lifetime. [Pg.370]

Spin-spin relaxation is the steady decay of transverse magnetisation (phase coherence of nuclear spins) produced by the NMR excitation where there is perfect homogeneity of the magnetic field. It is evident in the shape of the FID (/fee induction decay), as the exponential decay to zero of the transverse magnetisation produced in the pulsed NMR experiment. The Fourier transformation of the FID signal (time domain) gives the FT NMR spectrum (frequency domain, Fig. 1.7). [Pg.10]

The enzyme poised at well-defined redox potentials appears to be in rather homogenous IR states 65, 84). Curiously, in corresponding EPR-monitored experiments, the Ni signal generally corresponds to significantly less than one spin/mole, indicating that the sample is heterogeneous with respect to it (77). [Pg.296]

NMR spectrometers have improved significantly, particularly in the present decade, with the development of very stable superconducting magnets and of minicomputers that allow measurements over long time periods under homogeneous field conditions. Repetitive scanning and signal accumulation allow H-NMR spectra to be obtained with very small sample quantities. [Pg.9]


See other pages where Signal homogeneity is mentioned: [Pg.206]    [Pg.138]    [Pg.66]    [Pg.51]    [Pg.28]    [Pg.206]    [Pg.138]    [Pg.66]    [Pg.51]    [Pg.28]    [Pg.221]    [Pg.990]    [Pg.1441]    [Pg.1986]    [Pg.2482]    [Pg.2838]    [Pg.266]    [Pg.29]    [Pg.392]    [Pg.401]    [Pg.134]    [Pg.176]    [Pg.5]    [Pg.230]    [Pg.319]    [Pg.336]    [Pg.617]    [Pg.53]    [Pg.68]    [Pg.126]    [Pg.1017]    [Pg.446]    [Pg.1]    [Pg.73]    [Pg.295]    [Pg.104]    [Pg.54]    [Pg.556]    [Pg.825]    [Pg.982]    [Pg.92]    [Pg.84]    [Pg.90]    [Pg.416]    [Pg.671]    [Pg.13]    [Pg.16]    [Pg.77]    [Pg.382]    [Pg.249]   
See also in sourсe #XX -- [ Pg.28 ]




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