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Such errors in the coordination numbers will result in large errors in the calculated particle sizes.
One seeks to minimize bounds for the errors in the calculated results obtained from a given set of input data, exploiting analytical relations.
Band broadening in size exclusion chromatography (SEC) causes errors in the calculated molar mass distribution even when molar-mass-sensitive detectors are used.
This indicates that the large errors in the calculated ΔG hyd values of IHB molecules stem from the overestimation of attractive solute-water interactions.
Blue lines represent ± 0.4 × 10-4 s-1 and red lines represent ± 0.8 × 10-4 s-1 errors in the calculated rate constant.
A simplified model, presented in Fig. 8 was used to reduce errors in the calculated polarization resistance where RE is the resistance of the electrolyte measured at the high frequency intercept, the charge transfer resistance RCT measured at the low frequency intercept, and the capacitance of the ALD film C [28, 30].
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A systematic approach is presented for selection of appropriate domain size and element density for the finite-element simulations and for estimation of the error in the calculated ohmic resistance.
The use of a lower number of gray levels results in a higher error in the calculated contrast.
Note that differences in the spectra when attached to ParM may lead to a small error in the calculated concentrations.
The residual errors in the estimate were also calculated and confirmed to be small enough (∼50 µm) at each developmental stage.
Finally, the average error of the calculated torque in comparison to the study of Chertkiattipol and Niyamapa (2010), was 5%.
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