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@ARTICLE{Krachler:13329,
author = {Krachler, M. and Mohl, C. and Emons, H. and Shotyk, W.},
title = {{A}nalytical procedures for the determination of selected
trace elements in peat and plant samples by inductively
coupled plasma mass spectrometry},
journal = {Spectrochimica acta / B},
volume = {57},
issn = {0584-8547},
address = {Amsterdam [u.a.]},
reportid = {PreJuSER-13329},
pages = {1277 - 1289},
year = {2002},
note = {Record converted from VDB: 12.11.2012},
abstract = {A simple, robust and reliable analytical procedure for the
determination of 15 elements, namely Ca, V, Cr, Mn, Co, Ni,
Cu, Zn, Rb, Ag, Cd, Ba, Tl, Th and U in peat and plant
materials by inductively coupled plasma-quadrupole mass
spectrometry (ICP-QMS) was developed. Powdered sample
aliquots of approximately 220 mg were dissolved with various
acid mixtures in a microwave heated high-pressure autoclave
capable to digest 40 samples simultaneously. The selection
of appropriate amounts of digestion acids (nitric acid,
hydrofluoric acid or tetrafluoroboric acid) was crucial to
obtain accurate results. The optimized acid mixture for
digestion of plant and peat samples consisted of 3 ml HNO3
and 0.1 ml HBF4. An ultrasonic nebulizer with an additional
membrane desolvation unit was found beneficial for the
determination of Co, Ni, Ag, Tl, Th and U, allowing to
aspirate a dry sample aerosol into the ICP-QMS. A pneumatic
cross flow nebulizer served as sample introduction device
for the other elements. Internal standardization was
achieved with 103 Rh for all elements, except for Th whose
ICP-QMS signals were corrected by Rh-103 and Re-185. Quality
control was ascertained by analysis of the certified plant
reference material GBW 07602 Bush Branches and Leaves. In
almost all cases HNO3 alone could not fully liberate the
analytes of interest from the peat or plant matrix, probably
because of the silicates present. After adding small amounts
(0.05-0.1 ml) of either HF or HBF4 to the digestion mixture,
concentrations quantified by ICP-QMS generally increased
significantly, in the case of Rb up to $80\%.$ Further
increasing the volumes of HF or HBF4 in turn, resulted in a
loss of recoveries of almost all elements, some of which
amounted to approximately $60\%.$ The successful analytical
procedures were applied to the determination of two bulk
peat materials. In general, good agreement between the found
concentrations and results from an inter-laboratory trial or
from instrumental neutron activation data were obtained,
underpinning the suitability of the developed analytical
approach. (C) 2002 Elsevier Science B.V. All rights
reserved.},
keywords = {J (WoSType)},
cin = {ICG-III},
ddc = {540},
cid = {I:(DE-Juel1)VDB49},
pnm = {Chemie und Dynamik der Geo-Biosphäre},
pid = {G:(DE-Juel1)FUEK257},
shelfmark = {Spectroscopy},
typ = {PUB:(DE-HGF)16},
UT = {WOS:000178492500003},
doi = {10.1016/S0584-8547(02)00068-X},
url = {https://juser.fz-juelich.de/record/13329},
}