TY - GEN
T1 - Synthesis and characterization of bimetallic Ru-Re catalysts supported on oxide carriers
AU - Smykała, Szymon
AU - Adamska, Katarzyna
AU - Pawlyta, Mirosława
N1 - Publisher Copyright:
© 2020, Avestia Publishing. All rights reserved.
PY - 2020
Y1 - 2020
N2 - To be effective, synthesis of catalytic systems, consisting of metallic nanoparticles supported on oxide carriers has to be repeatable, efficient and at the same time, needs to produce samples of regular dispersion of active phase and precise elemental composition. With this, we present a relatively simple technique of synthesising bimetallic nanoparticles deposited on oxide carriers using microwave-assisted polyol approach. Morphology, microstructure and elemental composition of obtained catalysts were explored by transmission electron microscopy. Bimetallic Ru-Re system already proven to be effective in catalytic oxidation of short-chain hydrocarbons and are currently being tested in a soot combustion reaction. Introducing rhenium into ruthenium lattice increases catalysts dispersion and increases it’s stability [1]. Catalysts preparation started with dissolving appropriate amounts of precursors (RuCl3 and NH4ReO4) in ethylene glycol, then stirring overnight. After the dissolution of precursors, oxide powder was added to the solution. Oxide carriers we have chose included γ-Al2O3 and TiO2 in rutile and anatase phase. After further stirring, the mixture was poured into a Teflon tube which was placed inside a microwave reactor. Inside the reactor, in the presence of ethylene glycol and thanks to elevated temperature and pressure, reduction of ruthenium and rhenium ions occured. During this process, metallic nanoparticles are formed and, under the influence of microwaves, pushed inside the pores of the support. The obtained slurry was decanted and repeatedly washed with NaNO3 solution. Before the examination, all samples were treated with hydrogen for 3 hours under 400 °C. To examine catalysts structure evolution under an oxidizing atmosphere, we tested one sample after heating to 500 °C for 1 hour in the atmospheric air. Theoretical elemental compositions of catalysts were 2%Ru-0,8%Re and 5%Ru-2%Re. Catalysts characterisation was carried out using S/TEM TITAN 80-300 microscope equipped with EDAX EDS spectrometer. STEM images were collected with a 24.5-mrad probe semi-angle and recorded by HAADF detector at 47–200 mrad range. EDS analysis confirmed that synthesised catalysts compositions were in accordance with calculated values. In the case of the sample heated in air, no rhenium could be detected, which supports the concept of Re redispersion in elevated temperatures [2]. Z-contrast imaging allowed for unveiling catalysts morphology. We were able to tell how nanoparticles microstructure depends on which oxide support was chosen. Particles deposited on γ-Al2O3 could be characterised with spherical shapes without any tendency for agglomeration. On the other hand, such trends could be observed in catalysts supported on rutile, where nanoparticles formed arrays consisting of several smaller crystallites. This phenomenon was less apparent for anatase-supported samples, although increasing metal loading seems to promote this kind of behaviour. Sample heated in the atmospheric air had dramatically different morphology than reduced ones. It consisted of large (~50 nm) crystallites, which suggest, that the catalyst undergoes sintering in elevated temperatures under oxidising atmosphere.
AB - To be effective, synthesis of catalytic systems, consisting of metallic nanoparticles supported on oxide carriers has to be repeatable, efficient and at the same time, needs to produce samples of regular dispersion of active phase and precise elemental composition. With this, we present a relatively simple technique of synthesising bimetallic nanoparticles deposited on oxide carriers using microwave-assisted polyol approach. Morphology, microstructure and elemental composition of obtained catalysts were explored by transmission electron microscopy. Bimetallic Ru-Re system already proven to be effective in catalytic oxidation of short-chain hydrocarbons and are currently being tested in a soot combustion reaction. Introducing rhenium into ruthenium lattice increases catalysts dispersion and increases it’s stability [1]. Catalysts preparation started with dissolving appropriate amounts of precursors (RuCl3 and NH4ReO4) in ethylene glycol, then stirring overnight. After the dissolution of precursors, oxide powder was added to the solution. Oxide carriers we have chose included γ-Al2O3 and TiO2 in rutile and anatase phase. After further stirring, the mixture was poured into a Teflon tube which was placed inside a microwave reactor. Inside the reactor, in the presence of ethylene glycol and thanks to elevated temperature and pressure, reduction of ruthenium and rhenium ions occured. During this process, metallic nanoparticles are formed and, under the influence of microwaves, pushed inside the pores of the support. The obtained slurry was decanted and repeatedly washed with NaNO3 solution. Before the examination, all samples were treated with hydrogen for 3 hours under 400 °C. To examine catalysts structure evolution under an oxidizing atmosphere, we tested one sample after heating to 500 °C for 1 hour in the atmospheric air. Theoretical elemental compositions of catalysts were 2%Ru-0,8%Re and 5%Ru-2%Re. Catalysts characterisation was carried out using S/TEM TITAN 80-300 microscope equipped with EDAX EDS spectrometer. STEM images were collected with a 24.5-mrad probe semi-angle and recorded by HAADF detector at 47–200 mrad range. EDS analysis confirmed that synthesised catalysts compositions were in accordance with calculated values. In the case of the sample heated in air, no rhenium could be detected, which supports the concept of Re redispersion in elevated temperatures [2]. Z-contrast imaging allowed for unveiling catalysts morphology. We were able to tell how nanoparticles microstructure depends on which oxide support was chosen. Particles deposited on γ-Al2O3 could be characterised with spherical shapes without any tendency for agglomeration. On the other hand, such trends could be observed in catalysts supported on rutile, where nanoparticles formed arrays consisting of several smaller crystallites. This phenomenon was less apparent for anatase-supported samples, although increasing metal loading seems to promote this kind of behaviour. Sample heated in the atmospheric air had dramatically different morphology than reduced ones. It consisted of large (~50 nm) crystallites, which suggest, that the catalyst undergoes sintering in elevated temperatures under oxidising atmosphere.
UR - https://www.scopus.com/pages/publications/85097214304
U2 - 10.11159/icnnfc20.138
DO - 10.11159/icnnfc20.138
M3 - Conference contribution
AN - SCOPUS:85097214304
SN - 9781927877739
T3 - World Congress on Recent Advances in Nanotechnology
SP - 138
EP - 131
BT - Proceedings of the 5th World Congress on Recent Advances in Nanotechnology, RAN 2020
A2 - Ensinger, Wolfgang
PB - Avestia Publishing
T2 - 5th World Congress on Recent Advances in Nanotechnology, RAN 2020
Y2 - 11 October 2020 through 13 October 2020
ER -