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    Development of Active and Stable Low Nickel Content Catalysts for Dry Reforming of Methane
    (Basel : MDPI, 2017-5-16) Ha, Quan Luu Manh; Armbruster, Udo; Atia, Hanan; Schneider, Matthias; Lund, Henrik; Agostini, Giovanni; Radnik, Jörg; Vuong, Huyen Thanh; Martin, Andreas
    Methane dry reforming (DRM) was investigated over highly active Ni catalysts with low metal content (2.5 wt %) supported on Mg-Al mixed oxide. The aim was to minimize carbon deposition and metal sites agglomeration on the working catalyst which are known to cause catalyst deactivation. The solids were characterized using N2 adsorption, X-ray diffraction, temperature-programmed reduction, X-ray photoelectron spectroscopy, and UV-Vis diffuse reflectance spectroscopy. The results showed that MgO-Al2O3 solid solution phases are obtained when calcining Mg-Al hydrotalcite precursor in the temperature range of 550–800 °C. Such phases contribute to the high activity of catalysts with low Ni content even at low temperature (500 °C). Modifying the catalyst preparation with citric acid significantly slows the coking rate and reduces the size of large octahedrally coordinated NiO-like domains, which may easily agglomerate on the surface during DRM. The most effective Ni catalyst shows a stable DRM course over 60 h at high weight hourly space velocity with very low coke deposition. This is a promising result for considering such catalyst systems for further development of an industrial DRM technology.
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    Tracing Active Sites in Supported Ni Catalysts during Butene Oligomerization by Operando Spectroscopy under Pressure
    (Washington, DC : ACS, 2016) Rabeah, Jabor; Radnik, Jörg; Briois, Valérie; Maschmeyer, Dietrich; Stochniol, Guido; Peitz, Stephan; Reeker, Helene; La Fontaine, Camille; Brückner, Angelika
    Supported Ni catalysts have been studied during the dimerization of butenes by operando electron paramagnetic resonance (EPR) and in situ X-ray absorption spectroscopy (XAS) at 353 K and up to 16 bar. Single NiI/NiII shuttles were identified as active sites, whereby the conversion of initial NiI to NiII by oxidative addition of butene is obviously faster than the re-reduction of NiII to NiI by reductive elimination of the C8 product, rendering the equilibrium percentage of NiI small. At p ≤ 2 bar, NiI single sites form inactive Ni0 aggregates, while this is suppressed at higher pressure (∼12 bar). A reaction mechanism is proposed.
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    Chemical in-depth analysis of (Ca/Sr)F2 core–shell like nanoparticles by X-ray photoelectron spectroscopy with tunable excitation energy
    (Chichester [u.a.] : Wiley, 2021) Müller, Anja; Krahl, Thoralf; Radnik, Jörg; Wagner, Andreas; Kreyenschulte, Carsten; Werner, Wolfgang S.M.; Ritter, Benjamin; Kemnitz, Erhard; Unger, Wolfgang E.S.
    The fluorolytic sol–gel synthesis is applied with the intention to obtain two different types of core–shell nanoparticles, namely, SrF2–CaF2 and CaF2–SrF2. In two separate fluorination steps for core and shell formation, the corresponding metal lactates are reacted with anhydrous HF in ethylene glycol. Scanning transmission electron microscopy (STEM) and dynamic light scattering (DLS) confirm the formation of particles with mean dimensions between 6.4 and 11.5 nm. The overall chemical composition of the particles during the different reaction steps is monitored by quantitative Al Kα excitation X-ray photoelectron spectroscopy (XPS). Here, the formation of stoichiometric metal fluorides (MF2) is confirmed, both for the core and the final core–shell particles. Furthermore, an in-depth analysis by synchrotron radiation XPS (SR-XPS) with tunable excitation energy is performed to confirm the core–shell character of the nanoparticles. Additionally, Ca2p/Sr3d XPS intensity ratio in-depth profiles are simulated using the software Simulation of Electron Spectra for Surface Analysis (SESSA). In principle, core–shell like particle morphologies are formed but without a sharp interface between calcium and strontium containing phases. Surprisingly, the in-depth chemical distribution of the two types of nanoparticles is equal within the error of the experiment. Both comprise a SrF2-rich core domain and CaF2-rich shell domain with an intermixing zone between them. Consequently, the internal morphology of the final nanoparticles seems to be independent from the synthesis chronology.