heterogeneous catalysts
Recently Published Documents


TOTAL DOCUMENTS

3339
(FIVE YEARS 959)

H-INDEX

122
(FIVE YEARS 21)

2022 ◽  
Vol 57 ◽  
pp. 101879
Author(s):  
Wander Y. Perez-Sena ◽  
Kari Eränen ◽  
Narendra Kumar ◽  
Lionel Estel ◽  
Sébastien Leveneur ◽  
...  

JACS Au ◽  
2022 ◽  
Author(s):  
Daisuke Takei ◽  
Takafumi Yatabe ◽  
Tomohiro Yabe ◽  
Ray Miyazaki ◽  
Jun-ya Hasegawa ◽  
...  

Catalysts ◽  
2022 ◽  
Vol 12 (1) ◽  
pp. 91
Author(s):  
Jan Drönner ◽  
Peter Hausoul ◽  
Regina Palkovits ◽  
Matthias Eisenacher

The oxidation of cumene and following cleavage of cumene hydroperoxide (CHP) with sulfuric acid (Hock rearrangement) is still, by far, the dominant synthetic route to produce phenol. In 2020, the global phenol market reached a value of 23.3 billion US$ with a projected compound annual growth rate of 3.4% for 2020–2025. From ecological and economical viewpoints, the key step of this process is the cleavage of CHP. One sought-after way to likewise reduce energy consumption and waste production of the process is to substitute sulfuric acid with heterogeneous catalysts. Different types of zeolites, silicon-based clays, heteropoly acids, and ion exchange resins have been investigated and tested in various studies. For every type of these solid acid catalysts, several materials were found that show high yield and selectivity to phenol. In this mini-review, first a brief introduction and overview on the Hock process is given. Next, the mechanism, kinetics, and safety aspects are summarized and discussed. Following, the different types of heterogeneous catalysts and their performance as catalyst in the Hock process are illustrated. Finally, the different approaches to substitute sulfuric acid in the synthetic route to produce phenol are briefly concluded and a short outlook is given.


Gels ◽  
2022 ◽  
Vol 8 (1) ◽  
pp. 54
Author(s):  
Laura Riva ◽  
Angelo Davide Lotito ◽  
Carlo Punta ◽  
Alessandro Sacchetti

Herein we report the synthesis of cellulose-based metal-loaded nano-sponges and their application as heterogeneous catalysts in organic synthesis. First, the combination in water solution of TEMPO-oxidized cellulose nanofibers (TOCNF) with branched polyethyleneimine (bPEI) and citric acid (CA), and the thermal treatment of the resulting hydrogel, leads to the synthesis of an eco-safe micro- and nano-porous cellulose nano-sponge (CNS). Subsequently, by exploiting the metal chelation characteristics of CNS, already extensively investigated in the field of environmental decontamination, this material is successfully loaded with Cu (II) or Zn (II) metal ions. Efficiency and homogeneity of metal-loading is confirmed by scanning electron microscopy (SEM) analysis with an energy dispersive X-ray spectroscopy (EDS) detector and by inductively coupled plasma-optical emission spectrometry (ICP-OES) analysis. The resulting materials perform superbly as heterogeneous catalysts for promoting the reaction between aromatic aldehydes and alcohols in the synthesis of aromatic acetals, which play a fundamental role as intermediates in organic synthesis. Optimized conditions allow one to obtain conversions higher than 90% and almost complete selectivity toward acetal products, minimizing, and in some cases eliminating, the formation of carboxylic acid by-products. ICP-OES analysis of the reaction medium allows one to exclude any possible metal-ion release, confirming that catalysis undergoes under heterogeneous conditions. The new metal-loaded CNS can be re-used and recycled five times without losing their catalytic activity.


Biofuels ◽  
2022 ◽  
pp. 1-11
Author(s):  
Diego Oliveira Cordeiro ◽  
Janduir Egito da Silva ◽  
Jonh Anderson Macêdo Santos ◽  
Lindemberg de Jesus Nogueira Duarte ◽  
Francisco Wendell Bezerra Lopes ◽  
...  

2022 ◽  
Author(s):  
Charles Creissen ◽  
José Guillermo Rivera de la Cruz ◽  
Dilan Karapinar ◽  
Dario Taverna ◽  
Moritz Schreiber ◽  
...  

Electrochemical CO2 reduction presents a sustainable route to the production of chemicals and fuels. Achieving a narrow product distribution with copper catalysts is challenging and conventional material modifications offer limited control over selectivity. Here, we show that the mild cathodic potentials required to reach high currents in an alkaline gas-fed flow cell permits retention of a surface-bound thiol (4-mercaptopyridine), enabling molecule-directed selective formate generation at high reaction rates. Combined experimental and computational results showed that formate production is favoured due to the inhibition of a CO producing pathway caused by destabilising interactions with the anchored molecule. The immobilisation of molecules to inhibit specific carbon-based products therefore offers a novel approach to rationally tune the selectivity of heterogeneous catalysts.


2022 ◽  
Vol 32 (1) ◽  
Author(s):  
Carla S. Fermanelli ◽  
Adrián Chiappori ◽  
Liliana B. Pierella ◽  
Clara Saux

AbstractThe purpose of this work was to transform a regional biowaste into value-added chemicals and products through a modest thermo-catalytic pyrolysis process. ZSM-11 (Zeolite Socony Mobile-11) zeolites modified by nickel (Ni) incorporation (1–8 wt%) were synthesized and characterized by means of X-Ray Diffraction, Inductively Coupled Plasma Atomic Emission Spectroscopy, Infrared Fourier Transform Spectroscopy, UV–Vis Diffuse Reflectance Spectra and Temperature Programmed Reduction. Results demonstrated that Ni was mainly incorporated as oxide. These porous materials were evaluated as heterogeneous catalysts to improve biooil composition. In this sense, higher hydrocarbon yields, and quality chemicals were obtained and oxygenates were diminished. The deactivation of the most active material was studied over six cycles of reaction. In order to achieve the circular bioeconomy postulates, the obtained biochar (usually considered a residue) was further transformed through a physicochemical activation. The obtained activated biochars were extensively characterized.


Fuels ◽  
2022 ◽  
Vol 3 (1) ◽  
pp. 31-43
Author(s):  
Thomas Ruh ◽  
Richard Buchinger ◽  
Lorenz Lindenthal ◽  
Florian Schrenk ◽  
Christoph Rameshan

Catalytic tests to assess the performance of mixed perovskite-type oxides (La0.9Ca0.1FeO3-δ, La0.6Ca0.4FeO3-δ, Nd0.9Ca0.1FeO3-δ, Nd0.6Ca0.4FeO3-δ, Nd0.6Ca0.4Fe0.9Co0.1O3-δ, Nd0.6Ca0.4Fe0.97Ni0.03O3-δ, and LSF) with respect to CO oxidation are presented as well as characterization of the materials by XRD and SEM. Perovskites are a highly versatile class of materials due to their flexible composition and their ability to incorporate dopants easily. CO oxidation is a widely used “probe reaction” for heterogeneous catalysts. In this study, it is demonstrated how tuning the composition of the catalyst material (choice of A-site cation, A-site and B-site doping) greatly influences the activity. Changing the A-site cation to Nd3+ or increasing the concentration of Ca2+ as A-site dopant improves the performance of the catalyst. Additional B-site doping (e.g., Co) affects the performance as well—in the case of Co-doping by shifting ignition temperature to lower temperatures. Thus, perovskites offer an interesting approach to intelligent catalyst design and tuning the specific properties towards desired applications.


Sign in / Sign up

Export Citation Format

Share Document