Effect of initial nickel particle size on stability of nickel catalysts for aqueous phase reforming

The deactivation behavior by crystallite growth of nickel nanoparticles on various supports (carbon nanofibers, zirconia, SiC, α-Al2O3 and γ-Al2O3) was investigated in the aqueous phase reforming of ethylene glycol. Supported Ni catalysts of ∼10wt% were prepared by impregnation of carbon nanofibers...

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Veröffentlicht in:Journal of energy chemistry 2016-03, Vol.25 (2), p.289-296
Hauptverfasser: van Haasterecht, Tomas, Swart, Marten, de Jong, Krijn P., Bitter, Johannes Hendrik
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container_end_page 296
container_issue 2
container_start_page 289
container_title Journal of energy chemistry
container_volume 25
creator van Haasterecht, Tomas
Swart, Marten
de Jong, Krijn P.
Bitter, Johannes Hendrik
description The deactivation behavior by crystallite growth of nickel nanoparticles on various supports (carbon nanofibers, zirconia, SiC, α-Al2O3 and γ-Al2O3) was investigated in the aqueous phase reforming of ethylene glycol. Supported Ni catalysts of ∼10wt% were prepared by impregnation of carbon nanofibers (CNF), ZrO2, SiC, γ-Al2O3 and α-Al2O3. The extent of the Ni nanoparticle growth on various support materials follows the order CNF∼ZrO2>SiC>γ-Al2O3>>α-Al2O3 which sequence, however, was determined by the initial Ni particle size. Based on the observed nickel leaching and the specific growth characteristics; the particle size distribution and the effect of loading on the growth rate, Ostwald ripening is suggested to be the main mechanism contributing to nickel particle growth. Remarkably, initially smaller Ni particles (∼12nm) supported on α-Al2O3 were found to outgrow Ni particles with initially larger size (∼20nm). It is put forward that the higher susceptibility with respect to oxidation of the smaller Ni nanoparticles and differences in initial particle size distribution are responsible for this behavior. The extent of nickel particle growth was found to be related to the initial nickel particle size and small nickel particles supported on α-Al2O3 can outgrow nickel particles with a larger particle size. [Display omitted]
doi_str_mv 10.1016/j.jechem.2016.01.006
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Supported Ni catalysts of ∼10wt% were prepared by impregnation of carbon nanofibers (CNF), ZrO2, SiC, γ-Al2O3 and α-Al2O3. The extent of the Ni nanoparticle growth on various support materials follows the order CNF∼ZrO2&gt;SiC&gt;γ-Al2O3&gt;&gt;α-Al2O3 which sequence, however, was determined by the initial Ni particle size. Based on the observed nickel leaching and the specific growth characteristics; the particle size distribution and the effect of loading on the growth rate, Ostwald ripening is suggested to be the main mechanism contributing to nickel particle growth. Remarkably, initially smaller Ni particles (∼12nm) supported on α-Al2O3 were found to outgrow Ni particles with initially larger size (∼20nm). It is put forward that the higher susceptibility with respect to oxidation of the smaller Ni nanoparticles and differences in initial particle size distribution are responsible for this behavior. 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The extent of nickel particle growth was found to be related to the initial nickel particle size and small nickel particles supported on α-Al2O3 can outgrow nickel particles with a larger particle size. 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The extent of nickel particle growth was found to be related to the initial nickel particle size and small nickel particles supported on α-Al2O3 can outgrow nickel particles with a larger particle size. [Display omitted]</abstract><pub>Elsevier B.V</pub><doi>10.1016/j.jechem.2016.01.006</doi><tpages>8</tpages></addata></record>
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subjects Aqueous phase reforming
Carbon fibers
Catalysis
Catalyst stability
Catalysts
Leaching
Nanoparticles
Nickel
Nickel catalysts
Ostwald ripening
Particle growth
Particle size distribution
Particle size effect
Silicon carbide
Support effect
Zirconium dioxide
title Effect of initial nickel particle size on stability of nickel catalysts for aqueous phase reforming
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