Errors in an analytical method are often not recognized as such or are underrated. Therefore, it is useful to compile and publish them. Error tracking down can even be an exciting field of research. Two different errors which can occur in chromatography are presented: The area of poorly resolved peaks cannot be integrated accurately by the usual integrators or data systems due to geometrical reasons. Second, injected air can give rise to a retained peak in HPLC. Air injection can happen during a malfunction of the autosampler but the extra peak is unwanted because it can overlap with the analyte peaks
This spreadsheet demonstrates errors of partial integration of Gaussian peak using different rules. ...
These data are from a calibration of Acetic acid on a GC/FID instrument with a headspace autosampler...
There is a fundamental difference between data collected in comprehensive two-dimensional gas chroma...
Three graphs that indicate the relative error in peak area when two incompletely resolved peaks are ...
Chromatograms with overlapping peaks and a baseline rise or upset constitute a great challenge for a...
Various aspects of chromatographic peak quantitation and shape characterization are investigated in ...
In the recent years, the growing competition in the biopharmaceutical industry due to biosimilars co...
A peak-tracking algorithm for chromatograms recorded using liquid chromatography and mass spectromet...
A peak-tracking algorithm for chromatograms recorded using liquid chromatography and mass spectromet...
Due to the character of the original source materials and the nature of batch digitization, quality ...
A comprehensive study of the sources of systematic errors in the measurements of retention times has...
These data are from a calibration of Acetic acid on a GC/FID instrument with a headspace autosampler...
For pharmaceutical industry, HPLC is more than 40 years old. Even after instrumental advancements in...
Knowledge in organic chemistryThis program simulates the measurement error when dealing with peaks o...
in the pursuit of accuracy, especially in the exposure and reduction of the "big " errors ...
This spreadsheet demonstrates errors of partial integration of Gaussian peak using different rules. ...
These data are from a calibration of Acetic acid on a GC/FID instrument with a headspace autosampler...
There is a fundamental difference between data collected in comprehensive two-dimensional gas chroma...
Three graphs that indicate the relative error in peak area when two incompletely resolved peaks are ...
Chromatograms with overlapping peaks and a baseline rise or upset constitute a great challenge for a...
Various aspects of chromatographic peak quantitation and shape characterization are investigated in ...
In the recent years, the growing competition in the biopharmaceutical industry due to biosimilars co...
A peak-tracking algorithm for chromatograms recorded using liquid chromatography and mass spectromet...
A peak-tracking algorithm for chromatograms recorded using liquid chromatography and mass spectromet...
Due to the character of the original source materials and the nature of batch digitization, quality ...
A comprehensive study of the sources of systematic errors in the measurements of retention times has...
These data are from a calibration of Acetic acid on a GC/FID instrument with a headspace autosampler...
For pharmaceutical industry, HPLC is more than 40 years old. Even after instrumental advancements in...
Knowledge in organic chemistryThis program simulates the measurement error when dealing with peaks o...
in the pursuit of accuracy, especially in the exposure and reduction of the "big " errors ...
This spreadsheet demonstrates errors of partial integration of Gaussian peak using different rules. ...
These data are from a calibration of Acetic acid on a GC/FID instrument with a headspace autosampler...
There is a fundamental difference between data collected in comprehensive two-dimensional gas chroma...