by Keyword: conversion
Arnau, M, Turon, P, Aleman, C, Sans, J, (2023). Hydroxyapatite-based catalysts for CO2 fixation with controlled selectivity towards C2 products. Phenomenal support or active catalyst? Journal Of Materials Chemistry a 11, 1324-1334
Permanently polarized hydroxyapatite (p-HAp) has been reported as a feasible green alternative to conventional catalysts for the selective conversion of CO2 into highly valuable chemical products. However, structural control and enhanced electrical properties achieved on p-HAp clearly contrast with other reported catalytic systems, where hydroxyapatite mainly acts as a support receiving much less attention. In this work we take advantage of the knowledge obtained on p-HAp to develop an HAp-based catalytic system composed of TiO2 nanoparticles deposited on p-HAp. It is important to stress that p-HAp is not only considered as a mechanical support but has been put in the spotlight for catalyst preparation and as an active catalytic part. Therefore, the use of p-HAp in this system has unveiled exceptional synergies with TiO2 attributed to the enhanced electrical properties of p-HAp, capable of attracting the photo-electrons generated in TiO2 nanoparticles avoiding electron-hole recombination. CO2 fixation reactions carried out under mild conditions (120 degrees C, 6 bar and under UV exposure) result in complete selectivity control of the C2 products, shifting from ethanol (201 mu mol g(catalyst)(-1)) for p-HAp alone to acetic acid (381 mu mol g(catalyst)(-1)) when TiO2 nanoparticles are loaded in the system. Considering the challenging CO2 activation energy and the high control of the selectivity achieved, we do believe that this novel approach can be considered as a starting point to explore other systems and reactions where control of the crystal structure and the enhanced electrical properties of HAp can play a crucial role in the final products, reaction conditions, yields and selectivities.
JTD Keywords: Behavior, Cobalt, Conversion, Methane, Ni, Oxidation, Performance, Reduction, Syngas production, Tio2
Sans J, Arnau M, Sanz V, Turon P, Alemán C, (2022). Hydroxyapatite-based biphasic catalysts with plasticity properties and its potential in carbon dioxide fixation Chemical Engineering Journal 433, 133512
The design of catalysts with controlled selectivity at will, also known as catalytic plasticity, is a very attractive approach for the recycling of carbon dioxide (CO2). In this work, we study how catalytically active hydroxyapatite (HAp) and brushite (Bru) interact synergistically, allowing the production of formic acid or acetic acid depending on the HAp/Bru ratio in the catalyst. Raman, wide angle X-ray scattering, X-ray photoelectron spectroscopy, scanning electron microscopy and electrochemical impedance spectroscopy studies, combined with an exhaustive revision of the crystalline structure of the catalyst at the atomic level, allowed to discern how the Bru phase can be generated and stabilized at high temperatures. Results clearly indicate that the presence of OH– groups to maintain the crystalline structural integrity in conjunction with Ca2+ ions less bonded to the lattice fixate carbon into C1, C2 and C3 molecules from CO2 and allow the evolution from formic to acetic acid and acetone. In this way, the plasticity of the HAp-Bru system is demonstrated, representing a promising green alternative to the conventional metal-based electrocatalysts used for CO2 fixation. Thus, the fact that no electric voltage is necessary for the CO2 reduction has a very favorable impact in the final energetic net balance of the carbon fixation reaction. © 2021 ethanol production & nbsp
ethanol production & nbsp, brushite, co2 reduction, conversion, electrocatalytic reduction, electrode, formate, heterogeneous catalysis & nbsp, hydrogen evolution, insights, monetite, polarized hydroxyapatite,
Sans, Jordi, Sanz, Vanesa, Turon, Pau, Alemán, Carlos, (2021). Enhanced CO2 Conversion into Ethanol by Permanently Polarized Hydroxyapatite through C-C Coupling Chemcatchem 13, 5025-5033
JTD Keywords: added value chemicals, amino-acids, catalytic-hydrogenation, climate, design, electrochemical reduction, electroreduction, green co2 conversion to ethanol, nitrogen, photocatalytic reduction, polarized hydroxyapatite, recycling co2, sea-level, Acetone, Added value chemicals, Added-value chemicals, C-c coupling, Calcium apatites, Carbon dioxide, Carbon-dioxide, Co 2 reduction, Co2 reduction, Ethanol, Green co2 conversion to ethanol, Hard tissues, Hydroxyapatite, Mixtures, Morphology, Morphology and composition, Naturally occurring, Organic carbon, Phosphate minerals, Polarized hydroxyapatite, Recycling co2
Moreira VB, Puiggalí-Jou A, Jiménez-Piqué E, Alemán C, Meneguzzi A, Armelin E, (2021). Green nanocoatings based on the deposition of zirconium oxide: The role of the substrate Materials (Basel) 14,
© 2021 by the authors. Licensee MDPI, Basel, Switzerland. Herein, the influence of the substrate in the formation of zirconium oxide monolayer, from an aqueous hexafluorozirconic acid solution, by chemical conversion and by electro-assisted deposi-tion, has been approached. The nanoscale dimensions of the ZrO2 film is affected by the substrate nature and roughness. This study evidenced that the mechanism of Zr-EAD is dependent on the potential applied and on the substrate composition, whereas conversion coating is uniquely dependent on the adsorption reaction time. The zirconium oxide based nanofilms were more homogenous in AA2024 substrates if compared to pure Al grade (AA1100). It was justified by the high content of Cu alloying element present in the grain boundaries of the latter. Such intermetallic active sites favor the obtaining of ZrO2 films, as demonstrated by XPS and AFM results. From a mechanistic point of view, the electrochemical reactions take place simultaneously with the conventional chemical conversion process driven by ions diffusion. Such findings will bring new perspectives for the generation of controlled oxide coatings in modified electrodes used, as for example, in the construction of battery cells; in automotive and in aerospace industries, to replace micrometric layers of zinc phosphate by light-weight zirconium oxide nanometric ones. This study is particularly addressed for the reduction of industrial waste by applying green bath solutions without the need of auxiliary compounds and using lightweight ceramic materials.
JTD Keywords: aluminum alloys, conversion coating, electro-assisted deposition, metal-oxide interface, nanocoating, zirconium oxide, Aluminum alloys, Conversion coating, Electro-assisted deposition, Metal-oxide interface, Nanocoating, Zirconium oxide