Structural insights into ion conduction of layered double hydroxides with various proportions of trivalent cations

2013 ◽  
Vol 1 (46) ◽  
pp. 14569 ◽  
Author(s):  
Kohei Miyazaki ◽  
Yuya Asada ◽  
Tomokazu Fukutsuka ◽  
Takeshi Abe ◽  
Leonid A. Bendersky
2011 ◽  
Vol 184 (5) ◽  
pp. 1016-1024 ◽  
Author(s):  
Mohamed Mustapha Bouhent ◽  
Zoubir Derriche ◽  
Renaud Denoyel ◽  
Vanessa Prevot ◽  
Claude Forano

ChemSusChem ◽  
2010 ◽  
Vol 3 (8) ◽  
pp. 965-973 ◽  
Author(s):  
Qiang Wang ◽  
Hui Huang Tay ◽  
Desmond Jia Wei Ng ◽  
Luwei Chen ◽  
Yan Liu ◽  
...  

1994 ◽  
Vol 52 (1) ◽  
pp. 93-97 ◽  
Author(s):  
L. Indira ◽  
Mridula Dixit ◽  
P.Vishnu Kamath

2015 ◽  
Vol 76 (3) ◽  
Author(s):  
Siti Hasnawati Jamal ◽  
Wan Md Zin Wan Yunus ◽  
Noor Azilah Mohd Kasim ◽  
Ong Keat Khim ◽  
Mansor Ahmad

Layered double hydroxides (LDHs) has attracted much attention of many industrialists as well as academicians as these materials can be used as catalysts, adsorbents, anion exchangers, stabilizers and fillers for polymers. The materials which consist of divalent and trivalent cations, and anions are nontoxic and easy to prepare. In addition, the exchangeability of their anions makes them easy to be modified to increase their hydrophobicity property through anion exchange process using long chain surfactant anions. In this study, sodium lauryl ether sulphate (SLES) modified LDHs was prepared by co precipitation of LDHs and followed SLES ions modification via ion exchange process.  Intercalations of the anions into the LDHs layers were confirmed by X-ray diffraction analysis.  The presence of functional groups before and after modification was studied by FTIR spectrometry. Thermalgravitmeric analysis also was carried out to determine the amount of surfactant intercalated into LDHs.


2018 ◽  
Author(s):  
Diana Ainembabazi ◽  
Nan An ◽  
Jinesh Manayil ◽  
Kare Wilson ◽  
Adam Lee ◽  
...  

<div> <p>The synthesis, characterization, and activity of Pd-doped layered double hydroxides (Pd-LDHs) for for acceptorless amine dehydrogenation is reported. These multifunctional catalysts comprise Brønsted basic and Lewis acidic surface sites that stabilize Pd species in 0, 2+, and 4+ oxidation states. Pd speciation and corresponding cataytic performance is a strong function of metal loading. Excellent activity is observed for the oxidative transamination of primary amines and acceptorless dehydrogenation of secondary amines to secondary imines using a low Pd loading (0.5 mol%), without the need for oxidants. N-heterocycles, such as indoline, 1,2,3,4-tetrahydroquinoline, and piperidine, are dehydrogenated to the corresponding aromatics with high yields. The relative yields of secondary imines are proportional to the calculated free energy of reaction, while yields for oxidative amination correlate with the electrophilicity of primary imine intermediates. Reversible amine dehydrogenation and imine hydrogenation determine the relative imine:amine selectivity. Poisoning tests evidence that Pd-LDHs operate heterogeneously, with negligible metal leaching; catalysts can be regenerated by acid dissolution and re-precipitation.</p> </div> <br>


Sign in / Sign up

Export Citation Format

Share Document