Hi, I went through lots of literature and I could not find my answer. in the chromatogram we have lots of peaks and If I want to calculate the number of the theoretical plate to get the average peak capacity, what should I do? Which peak should I take?
Just in case the answer is still of interest, maybe for someone else: it doesn't matter. The number of theoretical plate is substance-independent, meaning it can be calculated off of every peak.
thanks for your perfect explanation🙏🏻 I have a question, at 10:50 you draw a chart for RB, what is this?
And why at 9:00 min, we have to change the baseline of the peaks?
Nice presentation.. Thankyou
Can you show how to export data containing the metadata (about selecting the baseline manually).
It looks like GC data not HPLC, if I am not wrong!
Thank you ! 😍
Hi, I went through lots of literature and I could not find my answer. in the chromatogram we have lots of peaks and If I want to calculate the number of the theoretical plate to get the average peak capacity, what should I do? Which peak should I take?
Just in case the answer is still of interest, maybe for someone else: it doesn't matter. The number of theoretical plate is substance-independent, meaning it can be calculated off of every peak.
Dear sir, please load the HPLC operation and calibration video.