Performance enhanced "tunable" capillary microwave-induced plasma mass spectrometer for gas chromatography detection

Citation
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
Citations number
21
Categorie Soggetti
Chemistry & Analysis","Spectroscopy /Instrumentation/Analytical Sciences
Journal title
ANALYTICAL CHEMISTRY
ISSN journal
00032700 → ACNP
Volume
72
Issue
14
Year of publication
2000
Pages
3102 - 3108
Database
ISI
SICI code
0003-2700(20000715)72:14<3102:PE"CMP>2.0.ZU;2-D
Abstract
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.