13 February 2019 2 8K Report

I have FTIR-ATR (GladiATR, 45°) absorption spectra of several PET foils that have been differently surface treated. The absorbance varies strongly from sample to sample and even between individual measurements of the same sample.

Now, I want to properly compare the individual spectra to one another. What is the proper procedure?

1. Rescale raw spectra so that one strong peak shows the same peak height / or peak area? How to properly do this in OPUS?

2. Background correct with what kind of function in OPUS?

Any suggestions?

Thanks!

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