Search results
Results from the WOW.Com Content Network
A calibration curve plot showing limit of detection (LOD), limit of quantification (LOQ), dynamic range, and limit of linearity (LOL).. In analytical chemistry, a calibration curve, also known as a standard curve, is a general method for determining the concentration of a substance in an unknown sample by comparing the unknown to a set of standard samples of known concentration. [1]
An example of a secondary standard is sodium hydroxide, a hydroscopic compound that is highly reactive with its surroundings. The concentration of a standard solution made with sodium hydroxide may fluctuate overtime due to the instability of the compound, requiring for calibration using a primary standard before use. [3] [5]
The δ values and absolute isotope ratios of common reference materials are summarized in Table 1 and described in more detail below. Alternative values for the absolute isotopic ratios of reference materials, differing only modestly from those in Table 1, are presented in Table 2.5 of Sharp (2007) [1] (a text freely available online), as well as Table 1 of the 1993 IAEA report on isotopic ...
The calibration curve that does not use the internal standard method ignores the uncertainty between measurements. The coefficient of determination (R 2 ) for this plot is 0.9985. In the calibration curve that uses the internal standard, the y-axis is the ratio of the nickel signal to the yttrium signal.
For example, the ionic strength of the solution can have an effect on the activity coefficients of the analytes. [3] [4] The most common approach for accounting for matrix effects is to build a calibration curve using standard samples with known analyte concentration and which try to approximate the matrix of the sample as much as possible. [2]
A list of chemical analysis methods with acronyms. A. Atomic absorption spectroscopy (AAS) Atomic emission spectroscopy (AES) Atomic fluorescence spectroscopy (AFS) ...
Using the calibration curve method, the analyst can calibrate the spectrometer with a pure silver aqueous solutions, and use the calibration graph to determine the amount of silver present in the waste samples. This method, however, assumes the pure aqueous solution of silver and a photographic waste sample have the same matrix and therefore ...
Figure 2 gives an example; in this example, the two x-intercepts differ by about 0.2 mL but this is a small discrepancy, given the large equivalence volume (0.5% error). Similar equations can be written for the titration of a weak base by strong acid (Gran, 1952; Harris, 1998).