Synthesis of γ-(Al1-xFex)2O3 solid solutions from oxinate precursors and formation of carbon nanotubes from the solid solutions using methane or ethylene as carbon source

This work reports for the first time the synthesis of γ-(Al1-xFex)2O3 solid solutions with a high specific surface area (200-230 m2/g) by the decomposition of metal oxinate [(Al1-xFex)(C9H6ON)3] and investigated the potential of these materials as catalysts for the synthesis of carbon nanotubes by c...

Full description

Saved in:
Bibliographic Details
Published in:Journal of materials research Vol. 23; no. 11; pp. 3096 - 3111
Main Authors: de Resende, Valdirene G., Cordier, Anne, De Grave, Eddy, Weibel, Alicia, Peigney, Alain, da Costa, Geraldo M., Laurent, Christophe, Vandenberghe, Robert E.
Format: Journal Article
Language:English
Published: New York, USA Cambridge University Press 01-11-2008
Springer International Publishing
Springer
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:This work reports for the first time the synthesis of γ-(Al1-xFex)2O3 solid solutions with a high specific surface area (200-230 m2/g) by the decomposition of metal oxinate [(Al1-xFex)(C9H6ON)3] and investigated the potential of these materials as catalysts for the synthesis of carbon nanotubes by catalytic chemical vapor deposition using methane or ethylene as carbon the source. The nanocomposite powders prepared by reduction in H2-CH4 contain carbon nanotubes (CNTs), which are mostly double-walled but also contain a fair amount of undesirable carbon nanofibers, hollow carbon particles, and metal particles covered by carbon layers. Moreover, abundant metallic particles are observed to cover the surfaces of the matrix grains. By contrast, the nanocomposite powders prepared by reduction in N2-C2H4 are not fully reduced, and the CNTs are much more abundant and homogeneous. However, they are multiwalled CNTs with a significant proportion of defects. The powders were studied by several techniques including Mössbauer spectroscopy and electron microscopy.
Bibliography:ark:/67375/6GQ-GRKF3FFW-M
istex:4D5B0664307244158474C4995326BC164147EC5F
PII:S0884291400030594
ArticleID:03059
ISSN:0884-2914
2044-5326
DOI:10.1557/JMR.2008.0379