Peter Kaden

Peter Kaden

orcid

Research Focus & Metrics

Academic Career Length

22Years (2005-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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23 March 2012 in Solvent Extraction and Ion Exchange
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Journal Article
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AGAndreas Geist
Andreas Geist
UMUdo Müllich
Udo Müllich
DMDaniel Magnusson
Daniel Magnusson
PKPeter Kaden
Peter Kaden
GMGiuseppe Modolo
Giuseppe Modolo
TZThomas Zevaco
Thomas Zevaco
i-SANEX is a process for separating actinides(III) from used nuclear fuels by solvent extraction: Actinides(III) and lanthanides(III) are co-extracted from a PUREX raffinate followed by selective back extraction of actinides(III) from the loaded organic phase. This step requires a complexing agent selective for actinides(III). A hydrophilic sulfonated bis triazinyl pyridine (SO3-Ph-BTP) was synthesized and tested for selective complexation of actinides(III) in nitric acid solution. When co-extracting Am(III) and Eu(III) from nitric acid into TODGA, adding SO3-Ph-BTP to the aqueous phase suppresses Am(III) extraction while Eu(III) is extracted. Separation factors in the range of 1000 are achieved. SO3-Ph-BTP remains active in nitric acid up to 2 mol/L. As a result of this performance, buffering or salting-out agents are not needed in the aqueous phase; nitric acid is used to keep the lanthanides(III) in the TODGA solvent. These properties make SO3-Ph-BTP a suitable candidate for i-SANEX process development.

2 March 2005 in Angewandte Chemie International Edition
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Journal Article
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PKPeter Kaden
Peter Kaden
EMElke Mayer‐Enthart
Elke Mayer‐Enthart
ATAnton Trifonov
Anton Trifonov
TFTorsten Fiebig
Torsten Fiebig
HWHans‐Achim Wagenknecht
Hans‐Achim Wagenknecht

10 June 2013 in Dalton Transactions
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Journal Article
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CAChristian Adam
Christian Adam
PKPeter Kaden
Peter Kaden
Björn Bertil BeeleBjörn Bertil Beele
Björn Bertil Beele
UMUdo Müllich
Udo Müllich
STSascha Trumm
Sascha Trumm
MDMelissa A. Denecke
Melissa A. Denecke
The molecular origin of the selectivity of N-donor ligands, such as alkylated bis-triazinyl pyridines (BTPs), for actinide complexation in the presence of lanthanides is still largely unclear. NMR investigations of an Am(nPrBTP)3 3+ complex with a 15N labelled ligand showed that it exhibits large differences in 15N chemical shift for coordinating N-atoms in comparison to both lanthanide(III) complexes and the free ligand. The temperature dependence of NMR chemical shifts observed for this complex indicates a weak paramagnetism. This fact and the observed large chemical shift for bound nitrogen atoms allow us to conclude that metal–ligand bonding in the reported Am(III) N-donor complex has a larger share of covalence than in lanthanide complexes. This may account for the observed selectivity.

1 May 2019 in Coordination Chemistry Reviews
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Journal Article
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LGLinda Götzke
Linda Götzke
GSGerrit Schaper
Gerrit Schaper
JMJuliane März
Juliane März
PKPeter Kaden
Peter Kaden
NHNina Huittinen
Nina Huittinen
JWJan J. Weigand
Jan J. Weigand

19 December 2014 in Chemical Science
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Journal Article
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CAChristian Adam
Christian Adam
Björn Bertil BeeleBjörn Bertil Beele
Björn Bertil Beele
AGAndreas Geist
Andreas Geist
UMUdo Müllich
Udo Müllich
PKPeter Kaden
Peter Kaden
PPPetra J. Panak
Petra J. Panak
NMR investigations of Am(C5-BPP)33+ show weak paramagnetism in Am(iii), indicating significant covalence in metal–ligand bonds with N-donor ligands. This may explain the observed extraction selectivity for actinides over lanthanides.

10 February 2022 in Journal of the American Chemical Society
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Journal Article
Closed access
KLKai Lv
Kai Lv
CUChristian Urbank
Christian Urbank
MPMichael Patzschke
Michael Patzschke
JMJuliane März
Juliane März
PKPeter Kaden
Peter Kaden
MSMoritz Schmidt
Moritz Schmidt