Journal
ANALYTICAL CHEMISTRY
Volume 78, Issue 6, Pages 1883-1889Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ac0518957
Keywords
-
Categories
Ask authors/readers for more resources
A method, based on inductively coupled plasma sector field mass spectrometry coupled with a microflow nebulizer and a desolvation system, has been developed for the direct determination of rare earth elements (REE) (La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu) down to the subpicogram per gram level (1 pg/g = 10(-12) gg(-1)) in similar to 1 mL of molten Antarctic ice. Contamination problems were carefully taken into account by adopting ultra-clean procedures during the sample pretreatment phases. The use of a desolvation system for sample introduction during the analysis greatly reduced spectral interferences from oxide formation; the residual interfering contributions were calculated and subtracted whenever necessary. A matched calibration curve method was used for the quantification of the analytes. Instrumental detection limits ranged from 0.001 pg/g for Ho, Tm, and Lu to 0.03 pg/g for Gd. The precision, in terms of relative standard deviation on 10 replicates, ranged from 2% for La, Ce, Pr, and Lu, up to 10% for Er, Tm, and Yb. This methodology allowed the direct determination of REE in a 1-mL sample of ancient Antarctic ice with concentration ranges between 0.006 and 0.4 pg/g for Tm and 0.9-60 pg/g for Ce.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available