Catalytic properties of BF3-treated aluminas III. Influence of precalcination temperature on the product selectivity in 1-butene isomerization and n-BuOH dehydration

1971 ◽  
Vol 23 (3) ◽  
pp. 395-397 ◽  
Author(s):  
K MATSUURA
RSC Advances ◽  
2018 ◽  
Vol 8 (33) ◽  
pp. 18663-18671 ◽  
Author(s):  
Guodong Liu ◽  
Jiaxu Liu ◽  
Ning He ◽  
Cuilan Miao ◽  
Jilei Wang ◽  
...  

Silicalite-1 zeolite was successfully acidified by zinc modification, the prepared Znx/S-1 catalysts exhibited excellent catalytic performances in both isobutane dehydrogenation and butene isomerization reactions.


Catalysts ◽  
2020 ◽  
Vol 10 (2) ◽  
pp. 265 ◽  
Author(s):  
Filipe Gaspar ◽  
Carla D. Nunes

Selective oxidation of benzyl alcohol to benzaldehyde was carried out with MoO2 nanoparticles (MoO2 NPs). MoO2 NPs were synthesized by two different approaches and characterized by several techniques. The synthesis was done by a hydrothermal procedure using ethylenediamine and either Fe2O3 or hydroquinone. In the latter case, an additional calcination step under N2 was performed to eliminate passivating agents at the surface of the nanoparticles. The synthesized nanocatalysts showed similar catalytic properties, being efficient catalysts in the oxidation of benzyl alcohol. High substrate conversion and product selectivity were achieved under all tested conditions. Studies were conducted using two different oxidants: tert-butyl hydroperoxide and hydrogen peroxide, in our continuous effort to obtain more efficient catalysts for more sustainable catalytic processes. When H2O2 was used as the oxidant, 94% yield was achieved with 100% selectivity for benzaldehyde, which was a very promising result to undergo other studies with this system. Moreover, to elucidate some aspects of the reaction mechanism, a study was conducted, and it was possible to conclude that the reaction undergoes, to some extent, through a radical mechanism with both oxidants.


Molecules ◽  
2019 ◽  
Vol 24 (10) ◽  
pp. 1878 ◽  
Author(s):  
Zi-Cheng Fu ◽  
Cheng Mi ◽  
Yan Sun ◽  
Zhi Yang ◽  
Quan-Qing Xu ◽  
...  

We present two as-synthesized Fe(II)-based molecular catalysts with 1,10-phenanthroline (phen) ligands; Fe(phen)3Cl2 (1) and [Fe(phen)2(CH3CH2OH)Cl]Cl (2), and their robust catalytic properties for the conversion of CO2 to CO in DMF/TEOA (DMF = N,N’-dimethylformamide; TEOA = triethanolamine) solution containing Ru(bpy)32+ and BIH (1,3-dimethyl-2-phenyl-2,3- dihydro-1H-benzo-[d]-imidazole). High turnover numbers (TONs) of 19,376 were achieved with turnover frequencies (TOFs) of 3.07 s−1 for complex 1 (1.5 × 10−7 M). A quantum efficiency of 0.38% was observed after 5 h irradiated by 450 nm monochromatic light. The generation rate of CO2 and H2 were tuned by optimizing the experimental conditions, resulting in a high CO selectivity of 90%. The remarkable contribution of the photosensitizer to the total TONCO was found being 19.2% (as shown by tests under similar conditions without catalysts) when BIH was employed as a sacrificial electron donor. The product selectivity in complex 2 reached 95%, and the corresponding TONCO and TOFCO were 33,167 and 4.61 s−1 in the same concentration with complex 1 used as catalyst; respectively. This work provides guidance for future designs of simple, highly efficient and selective molecular catalytic systems that facilitate carbon-neutral solar-to-fuel conversion processes


Author(s):  
L.D. Schmidt ◽  
K. R. Krause ◽  
J. M. Schwartz ◽  
X. Chu

The evolution of microstructures of 10- to 100-Å diameter particles of Rh and Pt on SiO2 and Al2O3 following treatment in reducing, oxidizing, and reacting conditions have been characterized by TEM. We are able to transfer particles repeatedly between microscope and a reactor furnace so that the structural evolution of single particles can be examined following treatments in gases at atmospheric pressure. We are especially interested in the role of Ce additives on noble metals such as Pt and Rh. These systems are crucial in the automotive catalytic converter, and rare earths can significantly modify catalytic properties in many reactions. In particular, we are concerned with the oxidation state of Ce and its role in formation of mixed oxides with metals or with the support. For this we employ EELS in TEM, a technique uniquely suited to detect chemical shifts with ∼30Å resolution.


1986 ◽  
Vol 83 ◽  
pp. 619-621 ◽  
Author(s):  
F. Vergand ◽  
B. Iraqi ◽  
C. Bonnelle ◽  
E. Ramaroson ◽  
M.F. Guilleux ◽  
...  

1978 ◽  
Vol 39 (01) ◽  
pp. 193-200 ◽  
Author(s):  
Erwin F Workman ◽  
Roger L Lundblad

SummaryAn improved method for the preparation of bovine α-thrombin is described. The procedure involves the activation of partially purified prothrombin with tissue thromboplastin followed by chromatography on Sulfopropyl-Sephadex C-50. The purified enzyme is homogeneous on polyacrylamide discontinuous gel electrophoresis and has a specific activity toward fibrinogen of 2,200–2,700 N.I.H. U/mg. Its stability on storage in liquid media is dependent on both ionic strenght and temperature. Increasing ionic strength and decreasing temperature result in optimal stability. The denaturation of α-thrombin by guanidine hydrochloride was found to be a partially reversible process with the renatured species possessing properties similar to “aged” thrombin. In addition, the catalytic properties of a-thrombin covalently attached to agarose gel beads were also examined. The activity of the immobilized enzyme toward fibrinogen was affected to a much greater extent than was the hydrolysis of low molecular weight, synthetic substrates.


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