1) Adding new ions into PIKA to account for

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Presentation transcript:

1) Adding new ions into PIKA to account for marine organic aerosol ion fragments 2) Precautions for deciding when N containing ions  peaks in fits are real or not 4th HR-AMS Clinic, Boulder,CO Paola Massoli Aerodyne Research

1) Adding new ions into PIKA to account for marine organic aerosol ion fragments

HR-ToF data collected (V mode) in marine environment NaCl (m/z 58) Diff ~ 90 Hz Broad shape due to surface vaporization

…..and its isotope (Na37Cl, 1/3 of intensity of parent ion)

Found several “unknown” peaks in the MS Likely halide clusters (Cl, Br) containing metals because they are on the left side of the m/z (also in closed, surface vaporization)

Like this at m/z 125 (MnCl2)

How do I make sure my guessed mass is right ? Use the isotope ratios of Cl, Br etc…. If MnCl2 is real, there should be 1) MnClj37Cl at mz 127 (UMR value) 2) Mnj37ClCl at mz 129 (UMR value)

MnClj37Cl

Need to modify the HR ion lists

Still some unknowns….

Use mmass.exe (public software)

…once you fitted all the peaks (and properly modified HR batch, family and frag tables)

2) Precautions for deciding when N containing ions  peaks in fits are real or not

Average todo wave w/ C3H2N

No C3H2N….there seems to be a residual signal to be fitted

One run….no clear sign that C3H2N should be fitted

Look at Ar (m/z 40)

Look at SO (m/z 48)

Bottom line N containing peaks are small, and they usually fall in the tail of big signals. The “peak broadening” can be an issue here Look at average todo wave vs single run Evaluate peak shape using Ar and SO Look at time series and their noise Loot at correlation plots between main peak and small ion (eg C4H4 and C3H2N of slide 16) to see if they co-vary: if yes, the small ion is not real Use W mode if you have it 