Big Chemical Encyclopedia

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

Articles Figures Tables About

Temperature-time data calibration

The results of the calibration and reaction experiments are shown in table 8.1 [142]. In this table, t is the time during which a current of intensity /flows through the calibration resistance, V the measured potential drop across the resistance, and m the mass of sample. The values of ATad for the calibration and reaction experiments were determined from the corresponding temperature-time data, using the Regnault-Pfaundler method with 7], Tf, k, and Tc0 calculated from equations 7.12-7.15 (section 7.1). [Pg.133]

Salinity-Temperature-Pressure (Depth). Conductivity, temperature and pressure data were collected using a Plessey Systems CTD with model 8400 data logger. These sensors were interrogated five times per second for values of temperature, conductivity (salinity), and pressure (depth). Data were recorded during the down-cast using a lowering rate of 30 m min". Niskin bottle samples were taken on every other cast to provide temperature and salinity calibration. Nominal precision of the salinity, temperature and depth measurments was 0.02 g kg", 0.02 °C and 0.2 m, respectively. [Pg.274]

If measurements need to be made at a variety of heating rates during the day, recalibration each time can be a significant inconvenience. One approach to overcome this is to calibrate at 0°C/min. At first this may seem odd, but it does have some advantages. First, it means that experiments can be made at any heating rate, and then a correction may be applied to the data to take into account the heating rate used. This calibration methodology also benefits isothermal experiments (for example, in kinetic studies) as the isothermal temperatures are exactly calibrated as well. [Pg.28]

Composition The law of mass aclion is expressed as a rate in terms of chemical compositions of the participants, so ultimately the variation of composition with time must be found. The composition is determined in terms of a property that is measured by some instrument and cahbrated in terms of composition. Among the measures that have been used are titration, pressure, refractive index, density, chromatography, spectrometry, polarimetry, conduclimetry, absorbance, and magnetic resonance. In some cases the composition may vary linearly with the observed property, but in every case a calibration is needed. Before kinetic analysis is undertaken, the data are converted to composition as a function of time (C, t), or to composition and temperature as functions of time (C, T, t). In a steady CSTR the rate is observed as a function of residence time. [Pg.707]

The extrapolated values together with results of the second calibration method are shown in Table V. With the exception of cabbage, agreement to better than 0.2% was found in the results of the two methods for the various foods. The proper refluxing time, for a rapid determination, was then selected from the data for the high temperature extraction shown in the last four columns in Table V. The required times varied from 5 minutes for onions and carrots to 30 minutes for celery. The shortness of these times as compared with other methods illustrates the potential usefulness of the Fischer method as a rapid control method, even though its accuracy is uncertain. [Pg.50]

The development of a calibration model is a time consuming process. Not only have the samples to be prepared and measured, but the modelling itself, including data pre-processing, outlier detection, estimation and validation, is not an automated procedure. Once the model is there, changes may occur in the instrumentation or other conditions (temperature, humidity) that require recalibration. Another situation is where a model has been set up for one instrument in a central location and one would like to distribute this model to other instruments within the organization without having to repeat the entire calibration process for all these individual instruments. One wonders whether it is possible to translate the model from one instrument (old or parent or master. A) to the others (new or children or slaves, B). [Pg.376]

For longer boreholes the data may need to be synchronized by comparing the return temperature not with the current time step but with the time step— n, where n is the travel time. The error minimized is the sum square error of the difference between the calculated and measured borehole heat exchanger return temperature. We have set up the analyses procedure in such a way that it is easy to select discrete data-windows for the calibration. [Pg.186]

There are several improvements that can be made to the present calibration procedure. First of all the numerical grid in the DST model can be adjusted to yield more accurate results for short time step data. Secondly the accuracy of the calibration can be increased. At present error for any time step of the calibrated temperatures is A0.2-0.4 K, this should probably be decreased to about 0.1-0.2 K. [Pg.191]

Infrared data in the 1575-400 cm region (1218 points/spec-trum) from LTAs from 50 coals (large data set) were used as input data to both PLS and PCR routines. This is the same spe- tral region used in the classical least-squares analysis of the small data set. Calibrations were developed for the eight ASTM ash fusion temperatures and the four major ash elements as oxides (determined by ICP-AES). The program uses PLSl models, in which only one variable at a time is modeled. Cross-validation was used to select the optimum number of factors in the model. In this technique, a subset of the data (in this case five spectra) is omitted from the calibration, but predictions are made for it. The sum-of-squares residuals are computed from those samples left out. A new subset is then omitted, the first set is included in the new calibration, and additional residual errors are tallied. This process is repeated until predictions have been made and the errors summed for all 50 samples (in this case, 10 calibrations are made). This entire set of... [Pg.55]

Figure 2-9 Some kinetic data on Reaction 2-79. For two samples (C and D at 773 K), equilibrium is reached monotonically. In the third sample (H), the species concentrations do not evolve monotonically with time OH content first decreases away from equilibrium and then increases toward equilibrium. The reaction rate for sample H is significantly slower because of both low H20t and low temperature (equilibrium would require about 1000 minutes). Data are from Zhang et al. (1995) but recalculated using the calibrations of Zhang et al. (1997a). Figure 2-9 Some kinetic data on Reaction 2-79. For two samples (C and D at 773 K), equilibrium is reached monotonically. In the third sample (H), the species concentrations do not evolve monotonically with time OH content first decreases away from equilibrium and then increases toward equilibrium. The reaction rate for sample H is significantly slower because of both low H20t and low temperature (equilibrium would require about 1000 minutes). Data are from Zhang et al. (1995) but recalculated using the calibrations of Zhang et al. (1997a).
A C.P.D. method was adopted by Bosworth and Rideal (95, 119) to investigate the evaporation of Na from a W filament. Desorption was accompanied by a negative drift in the S.P. when the coated filament was held at a temperature in the range 610° to 795° K., and the resulting S.P.-time curves were converted into coverage-time curves by the use of calibration data previously obtained. The results represent the mutual effect of adsorption and desorption processes on the W filament. Hence, the heat of evaporation E wav iiaay be calculated from the temperature coefficient of... [Pg.112]


See other pages where Temperature-time data calibration is mentioned: [Pg.278]    [Pg.566]    [Pg.398]    [Pg.91]    [Pg.441]    [Pg.131]    [Pg.11]    [Pg.6]    [Pg.198]    [Pg.359]    [Pg.83]    [Pg.428]    [Pg.47]    [Pg.37]    [Pg.276]    [Pg.349]    [Pg.1136]    [Pg.2547]    [Pg.57]    [Pg.340]    [Pg.319]    [Pg.54]    [Pg.77]    [Pg.185]    [Pg.35]    [Pg.237]    [Pg.238]    [Pg.293]    [Pg.139]    [Pg.158]    [Pg.85]    [Pg.538]    [Pg.145]    [Pg.287]    [Pg.28]    [Pg.268]    [Pg.56]    [Pg.255]    [Pg.152]    [Pg.192]   
See also in sourсe #XX -- [ Pg.128 , Pg.130 ]




SEARCH



Temperature calibration

Temperature data

Time calibration

Time-temperature

© 2024 chempedia.info