Ethanol conversion into olefins and aromatics over HZSM-5 zeolite: Influence of reaction conditions and surface reaction studies

2016 ◽  
Vol 422 ◽  
pp. 266-274 ◽  
Author(s):  
Zilacleide S.B. Sousa ◽  
Cláudia O. Veloso ◽  
Cristiane A. Henriques ◽  
Victor Teixeira da Silva
2019 ◽  
Vol 193 ◽  
pp. 263-272 ◽  
Author(s):  
G.M. Cabello González ◽  
P. Concepción ◽  
A.L. Villanueva Perales ◽  
A. Martínez ◽  
M. Campoy ◽  
...  

1992 ◽  
Vol 57 (2) ◽  
pp. 248-254
Author(s):  
Jaroslav Burda ◽  
Michal Bureš ◽  
Čestmír Černý

The CNDO/2 method was applied to the investigation of the surface reaction occurring during the epitaxial growth of silicon single crystals. The aim of the work was to find silicon species from which the crystal growth is possible under the reaction conditions chosen to comply with the application of the CVD technological method. Calculations suggest that the SiH2, SiHCl and SiH3 species are feasible for the further growth.


2002 ◽  
Vol 56 (6) ◽  
pp. 238-255 ◽  
Author(s):  
Xenophon Verykios

Carbon dioxide reforming of methane to synthesis gas was studied over Ni-based catalysts. It is shown that, in contrast to other Ni-based catalysts which exhibit continuous deactivation with time-on-stream, the rate over the Ni/La2O3 catalyst increases during the initial 2-3 h of reaction and then tends to be essentially invariable, displaying very good stability. X-ray diffraction, hydrogen and CO uptake studies, as well as high resolution TEM indicate that, under reaction conditions, the Ni particles are partially covered by La2O2CO3 species which are formed by interaction of La2O2 with CO2. Catalytic activity occurs at the Ni- La2O2CO3 interface, while the oxycarbonate species participate directly by reacting with deposited carbon, thus restoring the activity of the Ni sites at the interface. XPS and FTIR studies provide evidence in support of this mechanistic scheme. It was also found that methane cracking on Ni sites and surface reaction between deposited carbon and oxycarbonate species are the rate determining steps in the reaction sequence. A kinetic model is developed based on this mechanistic scheme, which is found to predict satisfactorily the kinetic measurements.


2019 ◽  
Vol 10 (1) ◽  
Author(s):  
Sune Levin ◽  
Joachim Fritzsche ◽  
Sara Nilsson ◽  
August Runemark ◽  
Bhausaheb Dhokale ◽  
...  

Abstract Studying single catalyst nanoparticles, during reaction, eliminates averaging effects that are an inherent limitation of ensemble experiments. It enables establishing structure–function correlations beyond averaged properties by including particle-specific descriptors such as defects, chemical heterogeneity and microstructure. Driven by these prospects, several single particle catalysis concepts have been implemented. However, they all have limitations such as low throughput, or that they require very low reactant concentrations and/or reaction rates. In response, we present a nanofluidic device for highly parallelized single nanoparticle catalysis in solution, based on fluorescence microscopy. Our device enables parallel scrutiny of tens of single nanoparticles, each isolated inside its own nanofluidic channel, and at tunable reaction conditions, ranging from the fully mass transport limited regime to the surface reaction limited regime. In a wider perspective, our concept provides a versatile platform for highly parallelized single particle catalysis in solution and constitutes a promising application area for nanofluidics.


2011 ◽  
Vol 65 (3) ◽  
Author(s):  
Ahmed Bshish ◽  
Zahira Yaakob ◽  
Binitha Narayanan ◽  
Resmi Ramakrishnan ◽  
Ali Ebshish

AbstractProduction of hydrogen by steam-reforming of ethanol has been performed using different catalytic systems. The present review focuses on various catalyst systems used for this purpose. The activity of catalysts depends on several factors such as the nature of the active metal catalyst and the catalyst support, the precursor used, the method adopted for catalyst preparation, and the presence of promoters as well as reaction conditions like the water-to-ethanol molar ratio, temperature, and space velocity. Among the active metals used to date for hydrogen production from ethanol, promoted-Ni is found to be a suitable choice in terms of the activity of the resulting catalyst. Cu is the most commonly used promoter with nickel-based catalysts to overcome the inactivity of nickel in the water-gas shift reaction. γ-Al2O3 support has been preferred by many researchers because of its ability to withstand reaction conditions. However, γ-Al2O3, being acidic, possesses the disadvantage of favouring ethanol dehydration to ethylene which is considered to be a source of carbon deposit found on the catalyst. To overcome this difficulty and to obtain the long-term catalyst stability, basic oxide supports such as CeO2, MgO, La2O3, etc. are mixed with alumina which neutralises the acidic sites. Most of the catalysts which can provide higher ethanol conversion and hydrogen selectivity were prepared by a combination of impregnation method and sol-gel method. High temperature and high water-to-ethanol molar ratio are two important factors in increasing the ethanol conversion and hydrogen selectivity, whereas an increase in pressure can adversely affect hydrogen production.


Author(s):  
James F. Hainfeld ◽  
Kyra M. Alford ◽  
Mathias Sprinzl ◽  
Valsan Mandiyan ◽  
Santa J. Tumminia ◽  
...  

The undecagold (Au11) cluster was used to covalently label tRNA molecules at two specific ribonucleotides, one at position 75, and one at position 32 near the anticodon loop. Two different Au11 derivatives were used, one with a monomaleimide and one with a monoiodacetamide to effect efficient reactions.The first tRNA labeled was yeast tRNAphe which had a 2-thiocytidine (s2C) enzymatically introduced at position 75. This was found to react with the iodoacetamide-Aun derivative (Fig. 1) but not the maleimide-Aun (Fig. 2). Reaction conditions were 37° for 16 hours. Addition of dimethylformamide (DMF) up to 70% made no improvement in the labeling yield. A high resolution scanning transmission electron micrograph (STEM) taken using the darkfield elastically scattered electrons is shown in Fig. 3.


2010 ◽  
Vol 1247 ◽  
Author(s):  
Rocío Calderón-Villajos ◽  
Carlos Zaldo ◽  
Concepción Cascales

AbstractControlled reaction conditions in simple, template-free hydrothermal processes yield Tm-Lu2O3 and Tm-GdVO4 nanocrystals with well-defined specific morphologies and sizes. In both oxide families, nanocrystals prepared at pH 7 reaction media exhibit photoluminescence in ∼1.95 μm similar to bulk single crystals. For the lowest Tm3+ concentration (0.2 % mol) in GdVO4 measured 3H4 and 3F4 fluorescence lifetimes τ are very near to τrad.


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