Rapid atomic layer deposition of silica nanolaminates: synergistic catalysis of Lewis/Brønsted acid sites and interfacial interactions

Nanoscale ◽  
2013 ◽  
Vol 5 (23) ◽  
pp. 11856 ◽  
Author(s):  
Guoyong Fang ◽  
Jing Ma
Catalysts ◽  
2018 ◽  
Vol 8 (7) ◽  
pp. 292 ◽  
Author(s):  
Cong Wang ◽  
Xinyu Mao ◽  
Jennifer Lee ◽  
Tzia Onn ◽  
Yu-Hao Yeh ◽  
...  

A series of ZrO2-supported WOx catalysts were prepared using atomic layer deposition (ALD) with W(CO)6, and were then compared to a WOx/ZrO2 catalyst prepared via conventional impregnation. The types of sites present in these samples were characterized using temperature-programmed desorption/thermogravimetric analysis (TPD-TGA) measurements with 2-propanol and 2-propanamine. Weight changes showed that the WOx catalysts grew at a rate of 8.8 × 1017 W atoms/m2 per cycle. Scanning transmission electron microscopy/energy-dispersive spectroscopy (STEM-EDS) indicated that WOx was deposited uniformly, as did the 2-propanol TPD-TGA results, which showed that ZrO2 was completely covered after five ALD cycles. Furthermore, 2-propanamine TPD-TGA demonstrated the presence of three types of catalytic sites, the concentrations of which changed with the number of ALD cycles: dehydrogenation sites associated with ZrO2, Brønsted-acid sites associated with monolayer WOx clusters, and oxidation sites associated with higher WOx coverages. The Brønsted sites were not formed via ALD of WOx on SiO2. The reaction rates for 2-propanol dehydration were correlated with the concentration of Brønsted sites. While TPD-TGA of 2-propanamine did not differentiate the strength of Brønsted-acid sites, H–D exchange between D2O and either toluene or chlorobenzene indicated that the Brønsted sites in tungstated zirconia were much weaker than those in H-ZSM-5 zeolites.


Molecules ◽  
2021 ◽  
Vol 26 (7) ◽  
pp. 2015
Author(s):  
Łukasz Kuterasiński ◽  
Małgorzata Smoliło-Utrata ◽  
Joanna Kaim ◽  
Wojciech Rojek ◽  
Jerzy Podobiński ◽  
...  

The aim of the present paper is to study the speciation and the role of different active site types (copper species and Brønsted acid sites) in the direct synthesis of furan from furfural catalyzed by copper-exchanged FAU31 zeolite. Four series of samples were prepared by using different conditions of post-synthesis treatment, which exhibit none, one or two types of active sites. The catalysts were characterized by XRD, low-temperature sorption of nitrogen, SEM, H2-TPR, NMR and by means of IR spectroscopy with ammonia and CO sorption as probe molecules to assess the types of active sites. All catalyst underwent catalytic tests. The performed experiments allowed to propose the relation between the kind of active centers (Cu or Brønsted acid sites) and the type of detected products (2-metylfuran and furan) obtained in the studied reaction. It was found that the production of 2-methylfuran (in trace amounts) is determined by the presence of the redox-type centers, while the protonic acid sites are mainly responsible for the furan production and catalytic activity in the whole temperature range. All studied catalysts revealed very high susceptibility to coking due to polymerization of furfural.


2015 ◽  
Vol 119 (19) ◽  
pp. 10427-10438 ◽  
Author(s):  
Amber Janda ◽  
Bess Vlaisavljevich ◽  
Li-Chiang Lin ◽  
Shaama Mallikarjun Sharada ◽  
Berend Smit ◽  
...  

2003 ◽  
Vol 125 (46) ◽  
pp. 13964-13965 ◽  
Author(s):  
Weiguo Song ◽  
David M. Marcus ◽  
Saifudin M. Abubakar ◽  
Emma Jani ◽  
James F. Haw

2005 ◽  
Vol 7 (8) ◽  
pp. 1861-1869 ◽  
Author(s):  
Laetitia Oliviero ◽  
Alexandre Vimont ◽  
Jean-Claude Lavalley ◽  
Francisca Romero Sarria ◽  
Marina Gaillard ◽  
...  

2010 ◽  
Vol 114 (18) ◽  
pp. 8363-8374 ◽  
Author(s):  
Emiel J. M. Hensen ◽  
Dilip G. Poduval ◽  
D. A. J. Michel Ligthart ◽  
J. A. Rob van Veen ◽  
Marcello S. Rigutto

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