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The peak-to-average power ratio (PAPR) is the peak amplitude squared (giving the peak power) divided by the RMS value squared (giving the average power). [1] It is the square of the crest factor. When expressed in decibels , crest factor and PAPR are equivalent, due to the way decibels are calculated for power ratios vs amplitude ratios .
Chromatographic peak resolution is given by = + where t R is the retention time and w b is the peak width at baseline. The bigger the time-difference and/or the smaller the bandwidths, the better the resolution of the compounds.
Peak-to-trough ratio in pharmacokinetics is the ratio of peak (C max) and trough (C min) levels of a drug over its dosing interval (τ) at steady state.. Peak-to-trough ratio (PTR), also known as peak-to-trough variation or peak-to-trough fluctuation, is a parameter in pharmacokinetics which is defined as the ratio of C max (peak) concentration and C min (trough) concentration over a dosing ...
Various properties of ripple voltage may be important depending on application: the equation of the ripple for Fourier analysis to determine the constituent harmonics; the peak (usually peak-to-peak) value of the voltage; the root mean square (RMS) value of the voltage which is a component of power transmitted; the ripple factor γ, the ratio ...
The response factor can be expressed on a molar, volume or mass [1] basis. Where the true amount of sample and standard are equal: = where A is the signal (e.g. peak area) and the subscript i indicates the sample and the subscript st indicates the standard. [2]
Peak values can be calculated from RMS values from the above formula, which implies V P = V RMS × √ 2, assuming the source is a pure sine wave. Thus the peak value of the mains voltage in the USA is about 120 × √ 2, or about 170 volts. The peak-to-peak voltage, being double this, is about 340 volts.
The peak is "well-sampled", so that less than 10% of the area or volume under the peak (area if a 1D Gaussian, volume if a 2D Gaussian) lies outside the measurement region. The width of the peak is much larger than the distance between sample locations (i.e. the detector pixels must be at least 5 times smaller than the Gaussian FWHM).
The fundamental resolution equation is used in chromatography to help relate adjustable chromatographic parameters to resolution, and is as follows: . R s = [N 1/2 /4][(α-1)/α][k 2 '/(1+k 2 ')], where