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The removal of carbon monoxide by iron oxide nanoparticles

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TLDR
In this article, superfine Fe 2 O 3 nanoparticles were evaluated both as a catalyst and as an oxidant for carbon monoxide oxidation, and it was found that the nanoparticles are much more effective as carbon dioxide catalysts than the non-nano oxide powder.
Abstract
NANOCAT ® Superfine Fe 2 O 3 nanoparticles were evaluated both as a catalyst and as an oxidant for carbon monoxide oxidation. It was found that the nanoparticles are much more effective as carbon monoxide catalysts than the non-nano oxide powder. For the Fe 2 O 3 nanoparticles, the reaction order is first-order with respect to the partial pressure of carbon monoxide, and zero-order with respect to the partial pressure of oxygen. The apparent activation energy was 14.5 kcal mol −1 and the normalized reaction rate was 19 s −1  m −2 at 300 °C. In the absence of oxygen, Fe 2 O 3 nanoparticles oxidize carbon monoxide directly as an oxidant. The resulting reduced forms of Fe 2 O 3 also catalyze a disproportionation reaction for a considerable amount of carbon monoxide. The significant amount of carbon monoxide it can remove through the catalytic oxidation, direct oxidation, and the disproportionation reaction make it a very promising material in certain special applications, such as removing the carbon monoxide from a burning cigarette, where the potential toxicity of other, more conventional catalysts would be undesirable. The higher activity of Fe 2 O 3 nanoparticles over non-nano Fe 2 O 3 powders was attributed to a small particle size (3 nm), the presence of an hydroxylated phase of iron oxide (FeOOH), as revealed by both high resolution transmission electron microscopy (HRTEM) and a comparable study of FeOOH (goethite) powder.

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Citations
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Self‐Assembled 3D Flowerlike Iron Oxide Nanostructures and Their Application in Water Treatment

TL;DR: In this paper, the synthesis of novel 3D flower-like iron oxide nanostructures by an ethylene glycol (EG)-mediated self-assembly process is reported, which can be used to further understand the mechanism of self-organization and expand the applications of IR nanomaterials.
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Synthesis and catalytic properties of metal nanoparticles: Size, shape, support, composition, and oxidation state effects

TL;DR: In this paper, the authors examine the role played by the particle structure and morphology (size and shape), its chemical composition and oxidation state, and the effect of the cluster support.
Journal ArticleDOI

Catalytic Oxidation of Carbon Monoxide over Transition Metal Oxides

TL;DR: In this article, the kinetics and mechanism of CO oxidation on single and mixed oxides are examined, alongside the catalyst structures, in a review of the literature on carbon monoxide over oxide catalysts.
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Magnetic nanoparticles: Synthesis, stabilization, functionalization, characterization, and applications

TL;DR: A review focusing on the synthesis, protection, functionalization, characterization and applications of magnetic nanoparticles is presented in this article, with a focus on particle formation mechanism and recent modifications made on the synthesized monodisperse samples of relatively large quantities.
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Quasi-one-dimensional metal oxide materials—Synthesis, properties and applications

TL;DR: A comprehensive review of the state-of-the-art research activities that focus on the Q1D metal oxide systems and their physical property characterizations is provided in this paper, where a range of remarkable characteristics are organized into sections covering a number of metal oxides, such as ZnO, In2O3, SnO2,G a 2O3 and TiO2, etc., describing their electrical, optical, magnetic, mechanical and chemical sensing properties.
References
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Journal ArticleDOI

Intrinsic proton affinity of reactive surface groups of metal(hydr)oxides: application to iron(hydr)oxides.

TL;DR: In this paper, an improved method for the calculation of proton affinities of individual surface groups of metal (hydr)oxides has been developed for a refinement of the multi site complexation (MUSIC) model.
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Characterization of iron oxides by x-ray absorption at the oxygen K edgeusing a full multiple-scattering approach

TL;DR: In this paper, x-ray-absorption near-edge structure spectroscopy at the oxygen K edge was used to link the features present in the spectra of each iron oxide to its specific atomic arrangement and electronic structure.
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Numerical Modeling of a Deep, Fixed Bed Combustor

TL;DR: In this article, a computational model to evaluate the performance characteristics of a deep, fixed-bed combustor/gasifier utilizing whole trees as the source of fuel is presented, which is the heat source for a proposed steam-driven electric power plant.
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Structure of a Nanophase Iron Oxide Catalyst

TL;DR: In this article, the bulk and surface structures of a nanophase iron oxide catalyst with average particle size of 30 A were determined using X-ray absorption near-edge structure (XANES) spectra.
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Carbon deposition and activity changes over FeRu alloys during Fischer-Tropsch synthesis

TL;DR: In this article, the interaction of 3H/sub 2/CO at 1 atm and 573 to 673/sup 0/K with unsupported Ru, Fe, and RuFe alloy powders was investigated using x-ray photoelectron spectroscopy (XPS), secondary ion mass spectrometry (SIMS), and differential chemical kinetics.
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