Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Open-phase analysis

It is not always possible or desirable to used closed-phase analysis. Sometimes other constraints in an application mean that a fixed frame spacing is required, and sometimes it is simply not possible to find the instant of glottal closure with any degree of accuracy. What then happens if the LP analysis is performed over an arbitrary section of speech The main npshot of this is that the LP analysis will attempt to model the effect of the zeros in the glottal transfer function, and in doing so include the effect of the zeros in its poles. [Pg.377]


Weckhuysen and coworkers (Nijhuis et al., 2003) described equipment suitable for parallel Raman and UV-vis spectroscopic measurements. Openings on the opposite sides of a furnace allowed acquisition of Raman and UV-vis spectra through optical grade windows in a tubular quartz reactor. UV-vis spectra were recorded at 823 K. Gas-phase analysis was achieved with mass spectrometry and gas chromatography. A more advanced version of the design (Nijhuis et al., 2004) accommodates four optical fiber probes, placed at 10-mm vertical spacing along the tubular reactor. The temperature that the fibers can withstand is 973 K the reported spectra characterize samples at 823 K. [Pg.165]

T. Blanco, N. Maniasso, M.F. Gine, A.O. Jacintho, Liquid-liquid extraction in flow injection analysis using an open-phase separator for the spectrophotometric determination of copper in plant digests, Analyst 123 (1998) 191. [Pg.442]

Because of the general difficulty encountered in generating reliable potentials energy surfaces and estimating reasonable friction kernels, it still remains an open question whether by analysis of experimental rate constants one can decide whether non-Markovian bath effects or other influences cause a particular solvent or pressure dependence of reaction rate coefficients in condensed phase. From that point of view, a purely... [Pg.852]

The Nichols chart shown in Figure 6.26 is a rectangular plot of open-loop phase on the x-axis against open-loop modulus (dB) on the jr-axis. M and N contours are superimposed so that open-loop and closed-loop frequency response characteristics can be evaluated simultaneously. Like the Bode diagram, the effect of increasing the open-loop gain constant K is to move the open-loop frequency response locus in the y-direction. The Nichols chart is one of the most useful tools in frequency domain analysis. [Pg.175]

The efficiency obtained from an open tubular column can be increased by reducing the column radius, which, in turn will allow the column length to be decreased and, thus, a shorter analysis time can be realized. However, the smaller diameter column will require more pressure to achieve the optimum velocity and thus the reduction of column diameter can only be continued until the maximum available inlet pressure is needed to achieve the optimum mobile phase velocity. [Pg.388]

Steven Carr (SmithKline Beecham) has used microbore columns to desalt proteins prior to ES-MS (32). The pore diameter of PolyHEA used (usually 200 A) was selected so that all proteins of interest would elute at Vo with 50 mM formic acid. Only the Vo peak was allowed to flow into the ES-MS nebularizer the rest of the SEC effluent (including the salts) was diverted to waste by opening a microdumper valve between the column and the nebularizer. The properties of the mobile phase were quite compatible with ES-MS analysis. [Pg.265]

Hence, aside from a phase factor e, which the present analysis leaves open and which can be chosen at will, we conclude ... [Pg.401]

High performance liquid chromatography (HPLC) has been by far the most important method for separating chlorophylls. Open column chromatography and thin layer chromatography are still used for clean-up procedures to isolate and separate carotenoids and other lipids from chlorophylls and for preparative applications, but both are losing importance for analytical purposes due to their low resolution and have been replaced by more effective techniques like solid phase, supercritical fluid extraction and counter current chromatography. The whole analysis should be as brief as possible, since each additional step is a potential source of epimers and allomers. [Pg.432]

Figure 12.10 Analysis of SFG spectra from atop CO on Pt(lll) using a CO-saturated 0.1 M H2SO4 electrolyte and a scan rate of 5 mV/s. The (2 x 2) —3CO (- /l9 x - /l9)R23.4°— 13CO phase transition resulted in a jump in atop amplitude (a). Stark tuning (b) and peak width versus electrode potential data (c) are also shown. (Filled circles denote hnear Stark tuning behavior while open circles correspond to deviations from linear behavior during oxidation.)... Figure 12.10 Analysis of SFG spectra from atop CO on Pt(lll) using a CO-saturated 0.1 M H2SO4 electrolyte and a scan rate of 5 mV/s. The (2 x 2) —3CO (- /l9 x - /l9)R23.4°— 13CO phase transition resulted in a jump in atop amplitude (a). Stark tuning (b) and peak width versus electrode potential data (c) are also shown. (Filled circles denote hnear Stark tuning behavior while open circles correspond to deviations from linear behavior during oxidation.)...
Consequently, the major experimental options for the analyst are packed or capillary SFC, mobile phase with/without modifier and off-line or on-line mode, namely direct deposition (DD-SFC-FUR) vs. flowcell. Both small-bore packed columns and narrow-bore open-tubular columns have been used for SFC-FTIR analysis using a pressure-stable, thermostated, flow-cell or solvent elimination interfaces. [Pg.476]

For nonequilibrium statistical mechanics, the present development of a phase space probability distribution that properly accounts for exchange with a reservoir, thermal or otherwise, is a significant advance. In the linear limit the probability distribution yielded the Green-Kubo theory. From the computational point of view, the nonequilibrium phase space probability distribution provided the basis for the first nonequilibrium Monte Carlo algorithm, and this proved to be not just feasible but actually efficient. Monte Carlo procedures are inherently more mathematically flexible than molecular dynamics, and the development of such a nonequilibrium algorithm opens up many, previously intractable, systems for study. The transition probabilities that form part of the theory likewise include the influence of the reservoir, and they should provide a fecund basis for future theoretical research. The application of the theory to molecular-level problems answers one of the two questions posed in the first paragraph of this conclusion the nonequilibrium Second Law does indeed provide a quantitative basis for the detailed analysis of nonequilibrium problems. [Pg.83]

We began our analysis in Section II and ended it in Section VC2 by making the connection of the time- and energy-domain approaches to both coherence spectroscopy and coherent control. It is appropriate to remark in closing that new experimental approaches that combine time- and energy-domain techniques are currently being developed to provide new insights into the channel phase problem. We expect that these will open further avenues for future research. [Pg.186]

Gross phase changes are detectable by eye upon close inspection of products. The package of course gets in the way of such analysis, but if a product is truly suspect, it should be closely examined by opening and inspecting the full contents of the container. Ajar can be opened and its contents probed with a spatula without ruining the container. Close inspection of the... [Pg.236]


See other pages where Open-phase analysis is mentioned: [Pg.386]    [Pg.377]    [Pg.386]    [Pg.377]    [Pg.266]    [Pg.208]    [Pg.387]    [Pg.377]    [Pg.57]    [Pg.61]    [Pg.108]    [Pg.109]    [Pg.62]    [Pg.121]    [Pg.366]    [Pg.394]    [Pg.289]    [Pg.5]    [Pg.37]    [Pg.136]    [Pg.207]    [Pg.499]    [Pg.146]    [Pg.130]    [Pg.692]    [Pg.83]    [Pg.420]    [Pg.822]    [Pg.834]    [Pg.1009]    [Pg.207]    [Pg.550]    [Pg.147]    [Pg.245]   


SEARCH



Phase analysis

© 2024 chempedia.info