Materials Map

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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Centre de Coopération Internationale en Recherche Agronomique pour le Développement

in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (8/8 displayed)

  • 2023Synthesis of potassium polyferrite KxFeyOz heterogeneous catalyst for sunflower oil ethanolic transesterification1citations
  • 2015Improving the kinetics of the CO2 gasification of char through the catalyst/biomass integration concept17citations
  • 2015The catalyst/biomass integration concept for the direct thermo-catalytic conversion of biomass into either syngas or added-value moleculescitations
  • 2014Optimization of pyrolysis conditions for production of reductant charcoalcitations
  • 2014Optimization of quality of charcoal for steelmaking using statistical analysis approachcitations
  • 2012Improvement of charcoal yield by two-step pyrolysis on eucalyptus wood : A thermogravimetric study69citations
  • 2005Nanoscaled Sn and Pb particles aligned in Al2O3 tubes obtained from molecular precursors18citations
  • 2003The metastable, glasslike solid-state phase of HAlO and its transformation to Al/Al2O3 using a CO2 laser24citations

Places of action

Chart of shared publication
Ouédraogo, Igor W. K.
1 / 1 shared
Happi Tchuessa, Emma Brice
1 / 1 shared
Sawadogo, Balkissa
1 / 1 shared
Mouras, Sylvie
1 / 1 shared
Tchini Tanoh, Séverin
1 / 1 shared
Julbe, Anne
2 / 18 shared
Richardson, Yohan
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Tanoh, Séverin
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Eibner, Simon
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Broust, François
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Noumi, Eric Serge
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De Cassia Oliveira Carneiro, Angelica
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Rousset, Patrick
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Noumi, Eric Serges
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Ngollo Mateke, Jean-Aimé
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Collard, François-Xavier
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Elyounssi, Khalid
1 / 1 shared
Schütt, Olivier
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Frères, Jacqueline
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König, Peter
1 / 2 shared
Veith, Michael
2 / 12 shared
Huch, Volker
1 / 5 shared
Faber, Stefan
1 / 1 shared
Köppe, Ralf
1 / 1 shared
Hüfner, Stefan
1 / 1 shared
De Masi, Remo
1 / 1 shared
Schnöckel, Hansgeorg
1 / 1 shared
Andres, Kathrin
1 / 1 shared
Wolf, Yan
1 / 1 shared
Zimmer, Michael
1 / 2 shared
Chart of publication period
2023
2015
2014
2012
2005
2003

Co-Authors (by relevance)

  • Ouédraogo, Igor W. K.
  • Happi Tchuessa, Emma Brice
  • Sawadogo, Balkissa
  • Mouras, Sylvie
  • Tchini Tanoh, Séverin
  • Julbe, Anne
  • Richardson, Yohan
  • Tanoh, Séverin
  • Eibner, Simon
  • Broust, François
  • Noumi, Eric Serge
  • De Cassia Oliveira Carneiro, Angelica
  • Rousset, Patrick
  • Noumi, Eric Serges
  • Ngollo Mateke, Jean-Aimé
  • Collard, François-Xavier
  • Elyounssi, Khalid
  • Schütt, Olivier
  • Frères, Jacqueline
  • König, Peter
  • Veith, Michael
  • Huch, Volker
  • Faber, Stefan
  • Köppe, Ralf
  • Hüfner, Stefan
  • De Masi, Remo
  • Schnöckel, Hansgeorg
  • Andres, Kathrin
  • Wolf, Yan
  • Zimmer, Michael
OrganizationsLocationPeople

article

Nanoscaled Sn and Pb particles aligned in Al2O3 tubes obtained from molecular precursors

  • Blin, Joël
  • Schütt, Olivier
  • Frères, Jacqueline
  • König, Peter
  • Veith, Michael
  • Huch, Volker
Abstract

Tin and lead nanoparticles and metal sponges were prepared by reducing Me2Si(NtBu)2Sn (7) and Me2Si(NtBu)2Pb (9) with [H2AlOtBu] (3), [HAl(OtBu)2] (13), [H2AlOSiMe2tBu] (8), and [(Me2tBuSiO)2AlH] (15). Together with dihydrogen and the metals in their elemental state the monomeric compounds [Me2Si(NtBu)2Al(OSiMe2tBu)(THF)] (10) and [Me2-Si(NtBu)2Al(OtBu)(THF)] (11) can be obtained, to mention only two examples. Each monomer is stabilized by a THF molecule coordinated to aluminum, which on sublimation loses its donor molecule and dimerizes through Lewis acid-base interactions to the spiro compounds [Me2Si(NtBu)2AlO-SiMe2tBu]2 (12) and [Me2Si(NtBu)2AlOtBu]2 (4), respectively. The molecular structures of 10, 11, and 12 were determined by single-crystal X-ray diffraction techniques. The reduction of 7 at -115 °C is gradually indicated by a color change of the reaction mixtures from red to dark brown with increasing temperature and depending on the reducing agent used. The tin powders that were obtained were identified as ?-tin using X-ray powder diffraction techniques and their average crystallite size depends on the polarity of the solvent and hydride used. Under certain conditions metal sponges are formed. Pycnometric measurements were carried out on the tin and lead sponges. These showed almost the known densities for the metals when helium was used whereas significantly smaller ones were measured in water. Porous alumina membranes of different pore diameters were filled with tin and lead particles. Metal nanoparticles were prepared within the tubes of the membranes by reduction of the metal amides in the pores. The infiltration process can be repeated up to ten times increasing the amount of particles within the tubes monitored by SEM. The obtained brown or black membranes were characterized by SEM, EDX, and UV/Vis analysis. The filled membranes show sharp impervious ranges in the UV/ Vis spectrum between 270 and 525 nm and could therefore be used as wavelength filters. (Résumé d'auteur)

Topics
  • nanoparticle
  • porous
  • impedance spectroscopy
  • pore
  • compound
  • scanning electron microscopy
  • x-ray diffraction
  • aluminium
  • Energy-dispersive X-ray spectroscopy
  • tin
  • molecular structure
  • aligned