For this tip, let’s use the Manually Identify Peaks tool.
Let’s start by bringing channels into review, in this case one standard and one sample. I modified the chromatogram plot so that we see a stack plot of the standard as compared to the sample.
Open the processing method and integrate/calibrate the standard.
Then integrate/quantitate the sample.
We see that the third peak in the sample chromatogram is not identified and the Peak Type in the Peaks table is Unknown. Furthermore, there is no calculated amount for the component.
Let’s assume the peak at 8.033 minutes is peak 3. An easy way of identifying the peak and quantitating the component is to click the Manually Identify Peaks tool.
A marker with the peak name appears to right of the peak at the expected retention time.
Using the mouse, move the marker close to the apex of the peak. The peak is identified and the calculated amount is displayed.
You can save this result by going to the File menu and selecting Save, Result. This will be flagged as a manually saved result.
It’s that easy!
This procedure can be followed using the QuickStart or Pro interface.
需要協助嗎?聯絡Waters專家。