An Innovative Microwave Process for Nanocatalyst Synthesis

Author(s):  
Claudia Antonetti ◽  
Anna Maria Raspolli Galletti ◽  
Iginio Longo

The development of greener chemical processes is becoming more and more important because this approach moves towards sustainable methods and products, minimizing pollution and risks for human health and environment. In these perspectives, microwaves seem to fulfil these requirements; in this context, we have tested a novel method both for the synthesis of nanocatalysts and for thermal activation of catalytic reactions. Until now, microwave chemistry has been generally performed inside a closed metal cavity, i.e. a microwave oven, but this approach presents relevant drawbacks, in particular for large scale application. Recently, we have proposed a new, cheap, sustainable process for large scale preparation of nanocatalysts, overcoming the disadvantages of the current synthesis methods. This novel method has been successfully adopted for the preparation in situ of ruthenium, palladium and silver nanoparticles as colloids or on different supports. Our procedure is safe and cheap, enabling to obtain the utmost efficiency and control also for industrial application. The obtained nanocatalysts present small average diameters, good morphology and very narrow sizes distribution with an absolute reproducibility. The ruthenium nanocatalysts were tested in the selective hydrogenation of phenol to cyclohexanone and palladium nanocatalysts were tested in the selective hydrogenation of cinnamaldehyde to hydrocinnamaldehyde, and we obtained good performances in both reactions.

2004 ◽  
Vol 25 ◽  
pp. S422
Author(s):  
Natalia Csokova ◽  
Rostislav Skrabana ◽  
Hans-Dieter Liebig ◽  
Anna Mederlyova ◽  
Peter Kontsek ◽  
...  

2021 ◽  
Author(s):  
Sudershan Reddy Gondi

<div>A unique and novel synthetic method was developed to generate substituted</div><div>anilines from its benzyl azides having ortho/para electron withdrawing group (EWG),</div><div>and when these groups are at meta position gives aldehyde, instead. This approach is</div><div>an inexpensive, simple, fast, efficient at room temperature. This protocol is easily</div><div>amenable to large scale preparation.</div>


RSC Advances ◽  
2017 ◽  
Vol 7 (88) ◽  
pp. 56081-56086 ◽  
Author(s):  
Xin Fan ◽  
Songdong Li ◽  
Yuehuan Wu ◽  
Lin Niu

One novel method of preparing macro-porous silica microspheres on a large scale is presented here, which utilized spray drying silica/polymer composite particles and calcination.


2020 ◽  
Author(s):  
Sudershan Reddy Gondi

<div>A unique and novel synthetic method was developed to generate substituted</div><div>anilines from its benzyl azides having ortho/para electron withdrawing group (EWG),</div><div>and when these groups are at meta position gives aldehyde, instead. This approach is</div><div>an inexpensive, simple, fast, efficient at room temperature. This protocol is easily</div><div>amenable to large scale preparation.</div>


Catalysts ◽  
2021 ◽  
Vol 11 (12) ◽  
pp. 1513
Author(s):  
Pavol Lopatka ◽  
Michal Gavenda ◽  
Martin Markovič ◽  
Peter Koóš ◽  
Tibor Gracza

This work describes the total synthesis of jaspine B involving the highly diastereoselective Pd(II)-catalysed carbonylative cyclisation in the preparation of crucial intermediates. New conditions for this transformation were developed and involved the pBQ/LiCl as a reoxidation system and Fe(CO)5 as an in situ source of stoichiometric amount of carbon monoxide (1.5 molar equivalent). In addition, we have demonstrated the use of a flow reactor adopting proposed conditions in the large-scale preparation of key lactones.


2021 ◽  
Author(s):  
Sudershan Reddy Gondi

<div>A unique and novel synthetic method was developed to generate substituted</div><div>anilines from its benzyl azides having ortho/para electron withdrawing group (EWG),</div><div>and when these groups are at meta position gives aldehyde, instead. This approach is</div><div>an inexpensive, simple, fast, efficient at room temperature. This protocol is easily</div><div>amenable to large scale preparation.</div>


1969 ◽  
Vol 22 (03) ◽  
pp. 577-583 ◽  
Author(s):  
M.M.P Paulssen ◽  
A.C.M.G.B Wouterlood ◽  
H.L.M.A Scheffers

SummaryFactor VIII can be isolated from plasma proteins, including fibrinogen by chromatography on agarose. The best results were obtained with Sepharose 6B. Large scale preparation is also possible when cryoprecipitate is separated by chromatography. In most fractions containing factor VIII a turbidity is observed which may be due to the presence of chylomicrons.The purified factor VIII was active in vivo as well as in vitro.


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