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@ARTICLE{Berns:45074,
author = {Berns, A. and Vinken, R. and Bertmer, M. and Breitschwerdt,
A. and Schäffer, A.},
title = {{U}se of 15{N}-depleted artificial compost in bound residue
studies},
journal = {Chemosphere},
volume = {59},
issn = {0045-6535},
address = {Amsterdam [u.a.]},
publisher = {Elsevier Science},
reportid = {PreJuSER-45074},
pages = {649 - 658},
year = {2005},
note = {Record converted from VDB: 12.11.2012},
abstract = {Association of bound residues to soil humic matter may be
accomplished by different binding mechanisms such as
sequestration in hydrophobic interiors of the organic
material or covalent linkage to the organic matter. The
structures and chemical environments of compounds can be
observed by NMR spectroscopy. We applied 15N-NMR
spectroscopy to study the soil-bound residues of 15N-labeled
simazine. As the 15N-isotope has a low sensitivity and
natural abundance 15N-NMR experiments require long
measurement times and often result in low signal-to-noise
(S/N) ratios. Therefore, in addition to the use of
15N-labeled simazine, 15N-depleted compost was used to
reduce the amount of background signal and enhance the
sensitivity. The compost was produced from maize and wheat
plants grown on sand with 15N-depleted NH4NO3 as sole
nitrogen source. The plants were freeze-dried, ground and
mixed with sand for composting. After a composting period of
224 days analysis of the compost revealed a 15N-content of
267 ppm as opposed to a natural abundance of 3650 ppm.
Characterization of this artificial compost produced
parameter values similar to those of a natural compost. The
13C-NMR-spectra of the humic and fulvic acids during
different stages of maturity showed that there was a shift
from single-bond functional groups to more complex
double-bond and aromatic structures. Experiments with this
compost showed an increased signal intensity. The improved
sensitivity made it possible to obtain interpretable NMR
signals in contrast to experiments with 15N-simazine on
native soil where no signals were detectable. The data
indicated that the bound residues of simazine are composed
of metabolites resulting from N-dealkylation and triazine
ring destruction. Silylation of the bound residues showed a
very strong binding of the residues to the matrix as only a
small fraction could be solubilized.},
keywords = {Chromatography, Gel / Humic Substances: analysis / Magnetic
Resonance Spectroscopy: methods / Nitrogen Isotopes /
Pesticide Residues: chemistry / Simazine: chemistry / Soil:
analysis / Trimethylsilyl Compounds / Humic Substances (NLM
Chemicals) / Nitrogen Isotopes (NLM Chemicals) / Pesticide
Residues (NLM Chemicals) / Soil (NLM Chemicals) /
Trimethylsilyl Compounds (NLM Chemicals) / Simazine (NLM
Chemicals) / trimethylchlorosilane (NLM Chemicals) / J
(WoSType)},
cin = {ICG-IV},
ddc = {333.7},
cid = {I:(DE-Juel1)VDB50},
pnm = {Chemie und Dynamik der Geo-Biosphäre},
pid = {G:(DE-Juel1)FUEK257},
shelfmark = {Environmental Sciences},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:15792662},
UT = {WOS:000228890400007},
doi = {10.1016/j.chemosphere.2004.10.027},
url = {https://juser.fz-juelich.de/record/45074},
}