scholarly journals Highly Dispersed Sn-beta Zeolites as Active Catalysts for Baeyer–Villiger Oxidation: The Role of Mobile, In Situ Sn(II)O Species in Solid-State Stannation

ACS Catalysis ◽  
2021 ◽  
pp. 5984-5998
Author(s):  
Elise Peeters ◽  
Guillaume Pomalaza ◽  
Ibrahim Khalil ◽  
Arnaud Detaille ◽  
Damien P. Debecker ◽  
...  
2010 ◽  
Vol 72 ◽  
pp. 164-169 ◽  
Author(s):  
Daphiny Pottmaier ◽  
Sebastiano Garroni ◽  
Maria Dolors Barò ◽  
Marcello Baricco

Hydrogen storage in the solid state has shown increasing research and development, and recently an approach in mixing two hydride systems together by ball milling (reactive hydride composites) has been investigated in more detail, e.g. NaBH4 plus MgH2. Thermodynamic destabilization may occur by new compounds formation during dehydrogenation, e.g. MgB2. A study of the the role of O2/H2O contamination for the reaction 2NaBH4 + MgH2 ↔ 2NaH + MgB2 + 4H2 was conducted using in-situ X-ray powder diffraction. Desorption reaction is observed to begin by a competition of MgH2 and NaBH4 decomposition due to higher reactivity promoted by ball milling processing summed to O2/H2O contamination. Oxidation of NaBH4 into NaBO2 is observed to happen in higher degree than MgH2/Mg into MgO for the Na-Mg-B-H system.


Nanoscale ◽  
2017 ◽  
Vol 9 (34) ◽  
pp. 12573-12589 ◽  
Author(s):  
Mariano D. Susman ◽  
Yishai Feldman ◽  
Tatyana A. Bendikov ◽  
Alexander Vaskevich ◽  
Israel Rubinstein

In situ LSPR measurements establish the role of the nano Kirkendall effect in Cu nanoparticle oxidation.


2018 ◽  
Vol 307 ◽  
pp. 293-300 ◽  
Author(s):  
Keita Taniya ◽  
Ryota Mori ◽  
Atsushi Okemoto ◽  
Takafumi Horie ◽  
Yuichi Ichihashi ◽  
...  

2016 ◽  
Vol 267 ◽  
pp. 56-64 ◽  
Author(s):  
Charles A. Roberts ◽  
Louisa Savereide ◽  
David J. Childers ◽  
Torin C. Peck ◽  
Justin M. Notestein

2019 ◽  
Author(s):  
Przemyslaw Rzepka ◽  
Zoltán Bacsik ◽  
Andrew J. Pell ◽  
Niklas Hedin ◽  
Aleksander Jaworski

Formation of CO<sub>3</sub><sup>2-</sup> and HCO<sub>3</sub><sup>-</sup> species without participation of the framework oxygen atoms upon chemisorption of CO<sub>2</sub> in zeolite |Na<sub>12</sub>|-A is revealed. The transfer of O and H atoms is very likely to have proceeded via the involvement of residual H<sub>2</sub>O or acid groups. A combined study by solid-state <sup>13</sup>C MAS NMR, quantum chemical calculations, and <i>in situ</i> IR spectroscopy showed that the chemisorption mainly occurred by the formation of HCO<sub>3</sub><sup>-</sup>. However, at a low surface coverage of physisorbed and acidic CO<sub>2</sub>, a significant fraction of the HCO<sub>3</sub><sup>-</sup> was deprotonated and transformed into CO<sub>3</sub><sup>2-</sup>. We expect that similar chemisorption of CO<sub>2</sub> would occur for low-silica zeolites and other basic silicates of interest for the capture of CO<sub>2</sub> from gas mixtures.


2020 ◽  
Author(s):  
Nicolò Maria della Ventura ◽  
Szilvia Kalácska ◽  
Daniele Casari ◽  
Thomas Edward James Edwards ◽  
Johann Michler ◽  
...  

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