A previously reported method of analyzing solution residues by glow di
scharge mass spectrometry (GDMS) has been extended to the analysis of
petroleum. Results showed that cathode formation could not be achieved
simply by drying and pressing with a conductive host matrix (as in th
e case of the aqueous solutions), and an additional low-temperature as
hing step was incorporated to reduce the organic material to a dried r
esidue. The residue was pressed with a conducting host into a pin, whi
ch was subjected to conventional GDMS analysis. The results from two N
IST aqueous reference solutions were compared to those from two SPEX s
tandard reference oils; only small differences in relative ion yields
(less than 10% average) were observed between the two types of sample.
This is well within experimental error. By applying relative sensitiv
ity factors, good accuracy was obtained (better than 5% average error)
; this indicates minimal matrix effects. Good agreement was also obser
ved between results obtained by using the GDMS methodology and those o
btained using EPA-approved inductively coupled plasma optical emission
spectroscopy calibration curve procedures. One limitation noted in th
e GDMS analysis was the increased number and type of polyatomic interf
erences, presumably caused by the residual organic constituents of the
oil.