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The relative standard deviations of the method were found below 8% for the three elements.
The relative standard deviations of the method for intraday and interday were obtained 4 and 11%, respectively.
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gstandard deviation from Monte-Carlo sampling using validated standard deviations of the methods as boundaries.
The maximum relative standard deviation of the method was 1.43% (n = 5).
The mean time and the standard deviation of the method in the generation of all these single paths were about 0.2 and 0.07 s, respectively.
The detection limit (S/N=3) and the relative standard deviation of the method were 2 μmol L−1 H2O2 and <5% (n=10, 10 μmol L−1 H2O2), respectively.
The root mean square deviation of the method for prediction of eccentric compressive strength of both types of prisms differed by only 2.2 KN, thereby demonstrating the potential for this probabilistic approach.
The 3σ limit of detection at a preconcentration time of 30 min, and the relative standard deviation of the method were 4.5 × 10−9 M U VI) and >12% (n = 5, 5 × 10−8 M U VI)), respectively.
The relative standard deviation of the method that was used for monosaccharide and ethanol analysis was estimated to ≤10%% ag EtOH/g consumed glucose bBalanced ethanol yield; g EtOH/g glucose prior to fermentation cVolumetric ethanol productivity; g EtOH × l−1 × h−1.
For the determination of PCDD/Fs in blood, the standard deviation of the method was < 10% for most congeners and up to 25% near the LOD.
In contrast, some of the details including the lower limit of quantification, the linear range of quantification, the accuracy, and the relative standard deviation of the method used in the 2012 study are not available.
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