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f •: <br /> r3e <br /> 4.2.1 PRECISION <br /> Precision of the data is a measure of the spread of the data when more than one mea- <br /> surement is taken on the same sample.. For duplicate measurements, precision can be <br /> expressed as the relative percent difference (RPD). A quantitative definition of the <br /> ,z RPD is given below: <br /> RPD = x2-X1 x 100 <br /> (xl+x2)!2 <br /> ' where: xl = first duplicate point value <br /> w x2 = second duplicate point value <br /> The sampling frequency for precision measurements will be at a minimum of 1 in 20 or <br /> �. I per set. <br /> r- <br /> 4.2.2 ACCURACY <br /> .- Feer <br /> Accuracy is an assessment of the closeness of the measured value to the true value. <br /> i <br /> Accuracy of chemical test re:alts is assessed by spiking samples with known standards <br /> and establishing the average ,recovery. In general, for organics, two types of recoveries <br /> are measured: matrix spike'recoveries and surrogate spike recoveries. For a matrix <br /> ��. spike, known amounts of standard compounds identical to the compounds present in <br /> the sample of interest are added to the sample. For a surrogate spike, the standards <br /> are chemically similar but not identical to the compounds in the fraction being ana- <br /> lyzed. The purpose of the surrogate spike is to provide quality control on every sample <br /> by constantly monitoring for unusual matrix effects and gross sample processing errors. <br /> Fer inorganics, only matrix spikes are measured in general. A quantitative definitic.rn of <br /> average recovery is given below. <br /> For spiked samples, the recovery (R) can be defined as a measure of accuracy: <br /> R = (Ci - c)/(C, x vx x 10-3) <br /> i <br /> ti. where: <br /> co = measured concentration analyzed in the sample without the addition of a <br /> spike (mfg) <br /> cs = concentration of standard added to the sample (mg/kg) <br /> vs = amount of standard added to the sample (mg/kg) <br /> sF0316041wp1004-51 4-2 <br />