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CARBON 55 (2013) 375– 378
Effect of high temperature treatment on the topological micro-
Tongji University, Shanghai Key Laboratory of Special Artificial Micro-
structure of micro-coil carbon fibers
structure Materials and Technology, Shanghai 20092, China
Fa-yu Wua, Yan-wen Zhoua, Jun-wei Zhanga, Jin-hong Dub, Feng Lib a
Carbon aerogels were synthesized at room temperature by a
School of Materials Science and Engineering, University of Science and
Technology Liao Ning, 185 Qianshan Road, Anshan 114051, China b
Shenyang National Laboratory for Materials Science, Institute of Metal
Research, Chinese Academy of Sciences, 72 Wenhua Road, Shenyang 110016, China The topological microstructure of micro-coiled carbon fibers (MCFs) before and after high temperature treatment (HTT) was explored and characterized. Results suggested that as-grown MCFs had an annular ring-like structure in the cross section and a herringbone-like structure in the longitudinal section, but the orientation range of graphitic domains was wide. After HTT, the coiled fibers consisted of stacked pyramidal prisms of ordered graphitic domains. The apparent morphology of the coiled fibers
sol–gel polymerization route using resorcinol and formaldehyde as precursors, acetonitrile as solvent and hydrochloric acid as catalyst, followed by CO2 supercritical drying and carbonization. FT-IR, SEM, XRD and nitrogen adsorption were used to characterize the microstructure of the aerogels. Results showed that the carbon aerogels are graphite-like amorphous materials with nano-skeleton networks formed by nanoparticles around 40– 70 nm in diameter, whose specific surface area is up to 1300 m2 g
1
and lowest density about 0.050 g/cm3. The heat of
condensation and the catalytic action of hydrochloric acid made it possible to form gels at room temperature. The high surface area and low density of the as-prepared carbon aerogels were ascribed to a strong interaction between acetonitrile and –OH groups by hydrogen bonding. [New Carbon Materials 2012, 27(6): 462–468]
is a uniform spiral prism. The evolvement of the microstructure of MCFs after HTT was also confirmed by X-ray diffraction and Raman spectroscopy. The topological microstructure provides a reliable reference for the prediction of properties and projected
Synthesis and characterization of condensed poly-nuclear aro-
applications of the MCFs.
matic resin using heavy distillate from ethylene tar
[New Carbon Materials 2012, 27(6): 448–454]
Ming-bo
Wua,
Yang-yang
Shia,
Shi-bin
Lia,
Ning
Guoa,
Yu-wei Wanga, Jing-tang Zhenga, Jie-shan Qiub a
State Key Laboratory of Heavy Oil Processing, China University of
Effects of carbon nanotubes grafted on a carbon fiber surface on
Petroleum, Qingdao 266555, China
their interfacial properties with the matrix in composites
b
Xiu-ying Liu, Ying Song, Cun-mei Li, Fu-ping Wang
Chemical Engineering, Dalian University of Technology, Dalian 116024,
School of Chemical Engineering and Technology, Harbin 150001, China
Carbon Research Laboratory, State Key Lab of Fine Chemicals, School of
China Heat-resistant condensed poly-nuclear aromatic resin (COPNAR) was prepared using heavy distillate (>250 °C, named DO)
Carbon fibers (CFs) were oxidized by concentrated HNO3 and
from distilled ethylene tar (ET). The basic properties of ET, DO
then reacted with polyamidoamine dendrimers (PAMAM) with
and COPNAR were investigated by FT-IR, 1H NMR, TGA and ele-
an average molecular weight of 157 to form CF–PAMAM. The CF–
mental analysis. The structural parameters of DO and ET were
PAMAM was further reacted with oxidized carbon nanotubes
obtained by the improved Brown–Ladner method and the forma-
(CNTs) to form CF–PAMAM–CNTs that were used as the reinforce-
tion mechanism of the COPNAR from DO was deduced. Results
ment for epoxy resin-based composites. The functional groups
show that a superior heat-resistant COPNAR can be obtained
and structure of the CF–PAMAM–CNTs were examined by XPS,
from DO. The distillation of ET increases the heat resistance of
SEM and AFM, and their wettability and the tensile strength were
the COPNAR, and the reaction mechanism is confirmed to be an
investigated by contact angle measurements and single strand
acid-catalyzed positive ion-type polymerization.
extension respectively. The interfacial shear strength of the com-
[New Carbon Materials 2012, 27(6): 469–475]
posites was measured by a micro-debonding method. Results showed that, compared with CFs, the surface roughness, surface energy and tensile strength of the CF–PAMAM–CNTs were increased by 180%, 300% and 22%, respectively when the CNT content was 15 mass%. The interfacial shear strength of the composite reinforced with CF–PAMAM–CNTs was increased by 178% for
Purification of natural graphite by microwave assisted acid leaching Yu-feng Lia,b, Shi-fu Zhua, Lei Wangb
the same CNT content, which showed that the grafted nanotubes
a
improved the interfacial properties of the filler with the matrix.
China
[New Carbon Materials 2012, 27(6): 455–461]
b
Department of Materials Science, Sichuan University, Chengdu 610064, Deep-processing Laboratory of Graphite, Panzhihua University,
Panzhihua 617000, China
Preparation of carbon aerogels at room temperature using ace-
Natural graphite was leached under microwave irradiation by
tonitrile as solvent
acid mixtures containing HCl (12 M) and HNO3 (16 M). It was
Pei-di Wu, Bin Zhou, Ai Du, Zhi-hua Zhang, Guang-ming Wu, Jun
found that the purification efficiency was affected by microwave
Shen
power, reaction pressure, reaction time and the acid ratio. The