Abstract

The effectiveness of a collision-reaction interface (CRI) as instrumental device and the addition of oxygen in the composition of auxiliary gas were evaluated to minimize polyatomic species generated in plasma gas caused by direct introduction of fuel ethanol samples through spray chambers in inductively coupled plasma quadrupole mass spectrometry (ICP-QMS). The oxygen flow-rate was optimized as a compromise among signal counts, signal to background ratio (SBR), and background equivalent concentration (BEC). For 12.5 mL min−1 O2, ethanol samples diluted 20 times were introduced into the plasma and deposits of carbon compounds on the sampler and/or skimmer cones were not observed. The performance of CRI using H2 and He inserted through the sampler or skimmer cones was evaluated. Hydrogen gas added through the skimmer cone was more efficient to reduce blank and BEC values. This strategy was necessary to eliminate spectral interferences caused by 40Ar12C+, 40Ar16O+, 12C16O+, at isotopes 52Cr+, 56Fe+, 28Si+ and 24Mg+, respectively. Using matrix-matching calibration and Y internal standard, the optimized method was applied to the determination of Al, Ba, Co, Cr, Cu, Fe, Mg, Mn, Mo, Na, Ni, Pb, Sb, Si, V, and Zn in fuel ethanol. Accuracy of developed method was checked after addition/recovery tests. Recoveries and RSD (n = 12) for all elements varied within the 78–114% and 0.4–2% ranges, respectively. Limits of detection for all elements obtained by combining CRI and ICP-QMS were always better than 0.80 µg L−1 except for Si at 14 µg L−1.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call