Agilent Technologies 8453 Operator's Manual page 377

Uv-visible spectroscopy system
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• for valley-to-valley (VV) peaks, the area above the baseline, segmented with
• for tangent (T) peaks, the area above the reset baseline,
• for solvent (S) peaks, the area above the horizontal extension from the
• negative peaks that occur below the baseline have a positive area, as shown
Understanding Your Agilent ChemStation
vertical dropped lines from tick marks, as in
Figure 25
Area Measurement for Valley-to-Valley Peaks
last-found baseline point and below the reset baseline given to tangent (T)
peaks. A solvent peak may rise too slowly to be recognized, or there may be
a group of peaks well into the run which you feel should be treated as a
solvent with a set of riders. This usually involves a merged group of peaks
where the first one is far larger than the rest. The simple drop-line
treatment would exaggerate the later peaks because they are actually sitting
on the tail of the first one. By forcing the first peak to be recognized as a
solvent, the rest of the group is skimmed off the tail,
in
Figure 26
on page 104.
Integration
Peak Area Measurement
Figure 25
on page 103,
4
103

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