Publication:
Bimetallic (Pt-Ni) La-hexaaluminate catalysts obtained from aluminum saline slags for the dry reforming of methane

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Date

2021

Director

Publisher

Elsevier
Acceso abierto / Sarbide irekia
Artículo / Artikulua
Versión publicada / Argitaratu den bertsioa

Project identifier

AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PID2020-112656RB-C21/ES/recolecta

Abstract

This work describes the synthesis of platinum-nickel/lanthanum hexaaluminates (PtNi/LHA) and their performance in terms of stability and catalytic activity in the dry reforming of methane (DRM) at 973 K. An Al solution (9.40 g/L) obtained from an Al saline slag waste by acid extraction was used to synthesize the hexaaluminate by mixing with a stoichiometric amount of lanthanum nitrate and methanol/Peg400/PegMn400 under hydrothermal conditions at 493 K for 16 h. After calcination at 1473 K for 2 h, the presence of LHA was confirmed. Wet impregnation of the synthesized support was used to obtain an initial Ni/LHA catalyst (10 wt% NiO) and the modified PtNi/LHA catalysts (0.2–1 wt% Pt). The support and catalysts were characterized by X-ray diffraction (XRD), N2 adsorption at 77 K, temperature- programmed reduction (TPR), scanning electron microscopy (SEM) and transmission electron microscopy (HR- TEM). The analysis of the TPR patterns for the catalysts allowed the type of metal support interaction and NiO species to be determined, with a weak interaction with the support being observed in all cases. The presence of Pt promoted NiO reducibility. The PtNi/LHA catalysts synthesized were found to be active and very stable in the DRM reaction after reaction for 50 h. The catalytic behavior was evaluated from the CO2 and CH4 conversions, as well as the H2/CO selectivity, with values of between 89% and 92% in almost all the time range evaluated. The presence of Pt improved the stability and catalytic performance of Ni/LHA thus improving resistance to coke formation.

Keywords

PtNi/La-hexaaluminate, Carbon dioxide, Methane, Temperature-programmed reduction, Electron microscopy

Department

Zientziak / Institute for Advanced Materials and Mathematics - INAMAT2 / Ciencias

Faculty/School

Degree

Doctorate program

Editor version

Funding entities

The authors are grateful for financial support from the Spanish Ministry of Science and Innovation (MCIN/AEI/10.13039/ 501100011033) through project PID2020-112656RB-C21. JJTH thanks Universidad Pública de Navarra for a pre-doctoral grant. AG also thanks Santander Bank for funding via the Research Intensification Program.

© 2021 The Author(s). This is an open access article under the CC BY-NC-ND license

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