Am. Zapata et A. Robbat, Performance enhanced "tunable" capillary microwave-induced plasma mass spectrometer for gas chromatography detection, ANALYT CHEM, 72(14), 2000, pp. 3102-3108
Improvements in the stability and performance of a capillary microwave-indu
ced plasma-mass spectrometer (MIP-MS) were achieved by optimizing power tra
nsfer to the cavity using a tunable coaxial MIP. The MIP, operating at atmo
spheric pressure, was sustained with 30 mL/min He and 60 W of power, Measur
ement precision and sensitivity for the standard waveguide and coaxial syst
ems were determined using 16 organochlorine pesticide solutions separated b
y gas chromatography (GC), The linear dynamic range obtained with the tunab
le MIP-MS extended over 3 orders of magnitude, a 10 time improvement with r
espect to the standard MIP. Detection limits were between 3 and 19 pg of Cl
mol(-1) s(-1) 7 times lower than the detection limits obtained with the no
ntunable MIP-MS, Analysis of pesticides containing sulfur atoms was also po
ssible, further demonstrating multielement MIP-MS detection. Excellent accu
racy (10% recovery) and precision (5% RSD) were found for the detection of
the pesticides in a petroleum-contaminated reference soil. By placing the G
C column at the plasma expansion stage, molecular fragmentation of a mixtur
e of volatile organic compounds was also demonstrated. With the MS operated
in the selected ion monitoring mode, measurement sensitivity was similar t
o 500 pg/s per compound.