Catalysis Today 76 (2002) 3–10
Mechanical and chemical breaking of multiwalled
carbon nanotubes
Krisztián Niesz
a
, Andrea Siska
b
, István Vesselényi
b
, Klara Hernadi
b,∗
, Dóra Méhn
b
,
Gábor Galbács
c
, Zoltán Kónya
b
, Imre Kiricsi
b
a
Laboratoire de R.M.N., Facultés Universitaires Notre-Dame de la Paix, 61 rue de Bruxelles, B-5000 Namur, Belgium
b
Department of Applied and Environmental Chemistry, University of Szeged, Rerrich Béla tér 1, H-6720 Szeged, Hungary
c
Department of Inorganic and Analytical Chemistry, University of Szeged, Dóm tér 7, H-6720 Szeged, Hungary
Abstract
Catalytically prepared multiwall carbon nanotubes (MWNTs) were cut and functionalised by mechanical and/or chemical
methods. Products were characterised by transmission electron microscopy, infrared spectroscopy and BET method. It can
be concluded that physical and chemical breaking procedures complete each other very well. With certain MWNT samples
containing surface oxides preliminary investigations were done for testing them as catalyst support.
© 2002 Elsevier Science B.V. All rights reserved.
Keywords: Carbon nanotubes; Mechanical and chemical breaking; Surface functional groups; Pt/carbon catalyst
1. Introduction
In heterogeneous catalytic processes special effort
was made to prevent coke formation in the reaction
of hydrocarbons [1,2]. As concerns the morphology
of these deposits, many interesting results have been
published [3,4]. From the 1970s, carbon fibers have
careened to various applications and were investi-
gated expansively [5,6]. The discovery of carbon
tubules of nanometer size induced wide-ranging re-
search activity on their synthesis, characterisation
and possible applications [7–9]. Increasing effort
is also being spent on their modification. The first
modification of nanotubes occurs right after their
production during their purification. When oxidative
treatment is applied for the removal of amorphous
carbon several structural vacancies may form [10].
∗
Corresponding author. Fax: +36-62-544-619.
E-mail address: hernadi@chem.u-szeged.hu (K. Hernadi).
Decapping the tubes makes the interior accessible
for various molecules. This time partial destruction
of the nanotube structure takes place at the end of
the tubes [11]. In both cases mentioned, the struc-
tural imperfections are closed by functional groups
such as COOH, OH or C=O. However, their con-
centration, which is hardly measurable even by spec-
troscopic methods, is not sufficient for immediate
practical utilisations, e.g., using them as polymer
fillers [12]. In order to increase the number of active
sites (open ends) one has to cut the tubes into pieces.
This can be achieved both by chemical and physical
methods. Single-wall fullerene nanotube ropes were
cut into 100–300 nm lengths which formed a stable
colloidal suspension in water with the help of sur-
factants [13]. Also single-walled carbon nanotubes
(SWNTs) were dissolved in organic solutions by
derivatisation with thionychloride and octadecylamine
and were characterised by near-infrared spectroscopy
[14].
0920-5861/02/$ – see front matter © 2002 Elsevier Science B.V. All rights reserved.
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