Big Chemical Encyclopedia

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

Articles Figures Tables About

Digital trace

We see that the digital traces are shown on a different graph than the analog traces, but they share the same time axis. These traces show results similar to the expected results. [Pg.490]

Notice the attribute PUL5E=Un. This attribute determines the pulse width rather than the time constant of R4 and Cl. The results are shown on the following screen capture. To plot traces on different plots, add the first trace, select Plot and then Add Plot to Window to add a new plot add the second trace, select Plot and then Add Plot to Window to add a new plot and then add the third trace. Digital traces are automatically plotted on a separate section of the screen. [Pg.493]

The observed rate constant is calculated from the half-reaction time on the digitized traces ... [Pg.525]

It is interesting to trace the development of instrument automation over the relatively brief period of the past ten to fifteen years. Early in this period, a truly automated instrument was a rare and expensive item built around a costly dedicated minicomputer. Automated data collection and analysis from any instrument which was not automated at the factory was usually accomplished by digitizing the data and storing it on a transportable media such as paper tape. These data were then delivered and fed to a timeshare system of some sort on which the data reduction program ran and which printed a report and sometimes a plot of the data. Often a considerable time delay occured between the generation and the analysis of the data. The scientist was at the mercy of the computer elite who could implement his data logger and provide the necessary computer resources to analyze his data. The process was expensive, both in time and in money. [Pg.3]

The most popular method of measuring peak area is by integration. Integration is a method in which the series of digital values acquired by the data system as the peak is being traced are summed. The sum is thus a number generated and presented by the data system and is taken to be the peak area. See Figure 11.20. We will discuss in Chapters 12 and 13 exactly how this area is converted to the quantity of analyte in GC and HPLC and the issues involved. See Workplace Scene 11.7. [Pg.324]

Most of the techniques employed can be traced back to polarography, which was already in use in 1925, to determine the concentrations of organic molecules [3]. Technical developments in instrumentation (potentiostats) [4], the use of nonaque-ous electrolytes [5], and the digital control of experiments [6] led to the spread of electroanalytical techniques. For example, cyclic voltammograms are frequently and routinely used today to define the redox... [Pg.3]

This point is illustrated by a second example. A vapor-phase spectrum of propionitrile was obtained and its digitization is shown in Table III. For the sake of example, assume the scientist entered the 2246 cm peak as average rather than sharp. The interpretation would result in likelihoods of 0.90 for isocyanate and 0.30 for nitrile. Performing the interpretation with the tracing function turned on would quickly show that the rules base the distinction between isocyanate and propionitrile very heavily on the width of the peak in the vicinity of 2260 cm . Reinterpreting this spectrum with the correct, sharp width entered for the 2246 cm peak results in a nitrile likelihood of 0.50 and isocyanate of 0.40. [Pg.319]

A. Hayden, E. Niple, and B. Boyce, Determination of trace-gas amounts in plumes by the use of orthogonal digital filtering of thermal emission spectra, Appl. Opt., 35(16), 2802-2809 (1996). [Pg.436]

One-dimensional spectra obtained in these experiments can be compared to ID traces of nD NMR spectra but offering much better digital resolution and shorter acquisition times. On the negative side each trace needs to be acquired separately and thus, if several sites are to be inspected, a series of ID experiments must be performed. In practice, this exercise is preceded by careful inspection of standard two-dimensional COSY, TOCSY, NOESY or ROESY spectra and only the ambiguous assignments are tackled by combined ID techniques. [Pg.54]

The pulse looks correct. Usually waveforms from a digital circuit have edges close together. If we plot both Vin and Vo on the same graph, the two traces may be hard to distinguish. To see both waveforms clearly, we will add a plot. Select Plot and then Add Plot to Window from the Probe menus. A second plot will appear on the same window. Add the trace V (VO) ... [Pg.387]

Fig. 18 Effects of digitization of the convolved spectrum z(jc) on deconvolution. Trace (a) is the original spectrum o(x), trace (b) the convolved spectrum i(x). Traces (c)-(f) are the deconvolved spectra after digitizing the convolved spectrum using 6, 8, 10, and 12 bits, respectively. Fig. 18 Effects of digitization of the convolved spectrum z(jc) on deconvolution. Trace (a) is the original spectrum o(x), trace (b) the convolved spectrum i(x). Traces (c)-(f) are the deconvolved spectra after digitizing the convolved spectrum using 6, 8, 10, and 12 bits, respectively.
The birth of the microcomputer can actually be traced back to the development of the transistor. With early electronic devices and computers the system of storing digital information was based on the use of vacuum tubes. These were cumbersome, expensive, and used a tremendous amount of power. They were much faster than relays, however, they were considerably slower than anything produced under today s standards. With the development of the transistor a revolution in the design of computer systems ushered in the time when systems would become smaller and more capable and less costly. The transistor was faster than its predecessor, the vacuum tube, required less power and was much cheaper to develop and produce than the vacuum tube technology. [Pg.3]


See other pages where Digital trace is mentioned: [Pg.91]    [Pg.92]    [Pg.91]    [Pg.92]    [Pg.872]    [Pg.900]    [Pg.1617]    [Pg.269]    [Pg.302]    [Pg.699]    [Pg.246]    [Pg.183]    [Pg.184]    [Pg.177]    [Pg.236]    [Pg.1]    [Pg.11]    [Pg.93]    [Pg.29]    [Pg.383]    [Pg.208]    [Pg.213]    [Pg.335]    [Pg.315]    [Pg.7]    [Pg.259]    [Pg.199]    [Pg.162]    [Pg.69]    [Pg.228]    [Pg.47]    [Pg.291]    [Pg.242]    [Pg.100]    [Pg.473]    [Pg.490]    [Pg.146]    [Pg.210]    [Pg.210]    [Pg.135]   


SEARCH



© 2024 chempedia.info