I have analysed a plasma sample with BRUKER - alpha FTIR spectrometer by ATR method, using a ZnSe lens, which have provided a spectrum with obvious peaks bellow 1500 Cm-1. After repeating the analysis with BRUKER - VERTEX 70 FTIR spectrometer with a diamond lens, the peaks that I was counting on, bellow 1500, has disappeared. Both spectra have undergone normalization, background and baseline correction; However, even raw spectra shows the disappearance of the peaks. what could be the potential cause of this disappearance and how to correct it?

The spectra pictures are attached to the question

##Update: I have just noticed that the blood tube used earlier are coated with silicone, unlike those used in the latter samples; thanks to dr.O'Keefe who notified me about the presence of the silicon spectrum in the earlier analysis. 

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