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.
Nice presentation.. Thankyou
Thank you ! 😍
Can you show how to export data containing the metadata (about selecting the baseline manually).
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?
It looks like GC data not HPLC, if I am not wrong!
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.