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For pH = 12, the well-fitting kinetic equation for the data of NC was the pseudo-second-order equation.
The calibration graph was constructed by relating the peak amplitudes at 324.0 nm to the corresponding concentrations of MLT and the regression equation for the data was computed.
This value gives a measure of the error in estimates for individual values calculated by the regression equation for the data set.
No common equation for the data at ϕ= 1.0 could be found analogous to that for ϕ= 0.3 because the ignition delay times show no Arrhenius-like behavior.
We compared inside-bark volume estimates obtained from the selected taper equation with estimates obtained from a simple logarithmic volume equation for the data obtained in this study and the equations used by the Forest Inventory and Analysis program in the Pacific Northwest (FIA-PNW) in the state of California and western half of the states of Oregon and Washington.
The coefficient of determination (r) of the model was calculated, in order to choose the best-fit equation for the data set.
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The regression equations for the data were computed.
The principle of the V-cell was discussed, giving equations for the data interpretation.
The CFC was calculated with the equation: For these data, similar to the case for within-frequency phase synchronization analyses, we compared the PSI between the manipulation and the ITI periods.
Evaluating Equation (1) for the data represented in Figure 6 results in a KSV value of 4.7 ±0.7)×10 L mol−1.
Evaluating Equation (1) for the data represented in Figure 3 results in a KSV value of 9.7 ±1.5)×10 gDonor g−1Quencher.
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