Properties of Carbon Nanofibers Prepared from Polyacrylonitrile/Poly(methyl Methacrylate) Blend

2009 ◽  
Vol 79-82 ◽  
pp. 353-356
Author(s):  
Wei Pan ◽  
Yan Chen ◽  
Xiao Wei He
Keyword(s):  
Methyl Methacrylate ◽  
Carbon Nanofibers ◽  
Carbon Fibers ◽  
Nitrogen Atmosphere ◽  
Wet Spinning ◽  
X Ray Diffraction ◽  
X Ray ◽  
Poly Methyl Methacrylate ◽  
Graphite Crystallite ◽  
Raman Microspectrometry

The polyacrylonitrile(PAN)/poly (methyl methacrylate)(PMMA) blend fibers were prepared by wet-spinning technique and carbonized over the temperature range of 400-1000°C in nitrogen atmosphere. After carbonization of the blend fibers, the PMMA component removed and the PAN component left in the form of carbon nanofibers. Morphology of the carbon nanofibers were investigated via scanning electron microscopy (SEM), and the carbonization behavior of the fibers were examined via x-ray diffraction (XRD), Raman microspectrometry. The optimal condition made carbon fibers with great L/D ratio and diameter less than 200 nm. XRD and Raman spectra shows that the PAN/PMMA blend fibers treated at 600°C produced some graphite crystallite.

Study of the Surface Morphology and the Microstructure of PAN-Based Carbon Fibers

2011 ◽  
Vol 239-242 ◽  
pp. 1279-1282
Author(s):  
Xue Jun Zhang ◽  
Zan Han ◽  
Yan Hong Tian ◽  
Yan Feng Yang
Keyword(s):  
Electron Microscopy ◽  
Carbon Fibers ◽  
Interlayer Spacing ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Graphite Crystallite ◽  
Crystallite Sizes ◽  
Degree Of Graphitization ◽  
Better Than

The microstructure of two kinds of self-made PAN-based high-modulus carbon fibers (HMCF-1, HMCF-2) was studied by scanning electron microscopy (SEM), Raman spectroscopy, X-ray diffraction (XRD) and high resolution transmission electron microscopy (HRTEM), and was compared with that of T800 and M55J. The correlation of XRD and HRTEM in terms of graphite crystallite sizes and interlayer spacing of graphite layer was also investigated. The results show that the diameters of T800, HMCF-1 and HMCF-2 are almost the same (~5.20μm) and all of them are lager than that of M55J (~4.86μm). The crystal sizes and the degree of graphitization are in the order of HMCF-2>HMCF-1>M55J>T800, while the regularity of the lattice fringes of HMCF-2 is better than those of others.

scholarly journals Preparation and Characterization of Zinc Oxide (Zno)/Polymethyl Methacrylate (PMMA) Nanocomposites

2021 ◽  
Vol 04 (04) ◽  
Author(s):  
Jayashree Bagawade ◽  
Keyword(s):  
Zinc Oxide ◽  
Methyl Methacrylate ◽  
Zinc Oxide Nanoparticles ◽  
Nanocomposite Films ◽  
Oxide Nanoparticles ◽  
X Ray Diffraction ◽  
X Ray ◽  
Poly Methyl Methacrylate ◽  
Absorption Measurements

A series of novel zinc oxide / Poly (methyl methacrylate) nanocomposite films with different ZnO contents were prepared through inclusion of pre-synthesized zinc oxide nanoparticles. The physical composition and morphology of the as-prepared nanocomposites were studied by XRD and TEM. The TEM analyses revealed that the zinc oxide nanoparticles have a particle size of ~3–5 nm. X-ray diffraction proved the presence of the amorphous PMMA in the nanocomposites. The intermolecular interactions within the polymer nanocomposites were explored by FTIR and XRD. FTIR spectra confirmed the dispersion of the zinc oxide nanoparticles in the Poly (methyl methacrylate) i.e. PMMA matrices. The UV-Vis absorption measurements of the ZnO/PMMA nanocomposites proved their potential optical properties.

scholarly journals Microstructure evolution and properties of polyimide fibers containing trifluoromethyl units

2019 ◽  
Vol 32 (1) ◽  
pp. 39-46
Author(s):  
Hongqing Niu ◽  
Mengying Zhang ◽  
Ang Li ◽  
Ziqi Wang ◽  
Xiaodong Wang ◽  
...  
Keyword(s):  
Molecular Design ◽  
Nitrogen Atmosphere ◽  
Wet Spinning ◽  
Fiber Direction ◽  
X Ray Diffraction ◽  
X Ray ◽  
Polyimide Fibers ◽  
Initial Modulus ◽  
Molecular Alignments ◽  
Biphenyltetracarboxylic Dianhydride

A series of copolyimide (co-PI) fibers containing trifluoromethyl units were successfully obtained on the molecular design of 3,3′,4,4′-biphenyltetracarboxylic dianhydride, p-phenylenediamine, and 2,2-bis[4-(4-aminophenoxy)phenyl]hexafluoropropane (HFBAPP) via a widely utilized two-step wet-spinning method. Significant variations on the microstructures and properties of the resulting co-PI fibers were observed after the incorporation of HFBAPP moieties. The tensile strength and initial modulus of the fibers decreased from 0.70 GPa to 0.38 GPa and from 69.63 GPa to 9.60 GPa, respectively. However, the dielectric permittivity decreased from 3.62 to 2.85 in the frequency of 10 MHz as a result of the incorporation of trifluoromethyl units. Two-dimensional wide-angle X-ray diffraction showed that the fibers exhibited highly oriented molecular alignments along the fiber direction and low lateral packing degree in the transverse direction. In addition, the co-PI fibers possessed excellent thermal–oxidative stabilities with the 5% weight loss temperature ranging from 532°C to 552°C under nitrogen atmosphere and the glass transition temperature ranging from 312°C to 330°C.

Preparation, morphology, and microstructure of diameter-controllable vapor-grown carbon nanofibers

1998 ◽  
Vol 13 (8) ◽  
pp. 2342-2346 ◽  
Author(s):  
Yue-Ying Fan ◽  
Feng Li ◽  
Hui-Ming Cheng ◽  
Ge Su ◽  
Ying-Da Yu ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Carbon Nanofibers ◽  
Carbon Fibers ◽  
Fiber Axis ◽  
Duplex Structure ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
High Resolution Tem

Pure vapor-grown carbon nanofibers (VGCNF's) with controllable diameters of 10–200 nm were prepared by an improved floating catalyst method. Through transmission electron microscopy (TEM) observation, it was found that VGCNF's have a duplex structure, a hollow and high-crystallinity graphite filament called primary carbon fiber surrounded by a pyrocarbon layer with low graphite crystallinity. It was observed using high-resolution TEM that VGCNF's have excellent graphitic crystallinity with graphite layers stacked neatly parallel to fiber axis. Moreover, x-ray diffraction results showed that the graphitic crystallinity of carbon fibers became higher with decreasing diameter of carbon fibers.

scholarly journals Hydrogen desorption kinetics of MgH2 synthesized from modified waste magnesium

2014 ◽  
Vol 32 (3) ◽  
pp. 385-390
Author(s):  
Aysel Kantürk Figen ◽  
Bilge Coşkuner ◽  
Sabriye Pişkin
Keyword(s):  
Hydrogen Desorption ◽  
Nitrogen Atmosphere ◽  
Desorption Kinetics ◽  
X Ray Diffraction ◽  
Heating Rates ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Xrf Scanning ◽  
Isothermal Kinetic ◽  
Kinetics Of

AbstractIn the present study, hydrogen desorption properties of magnesium hydride (MgH2) synthesized from modified waste magnesium chips (WMC) were investigated. MgH2 was synthesized by hydrogenation of modified waste magnesium at 320 °C for 90 min under a pressure of 6 × 106 Pa. The modified waste magnesium was prepared by mixing waste magnesium with tetrahydrofuran (THF) and NaCl additions, applying mechanical milling. Next, it was investigated by X-ray diffraction (XRD), X-ray fluorescence (XRF), scanning electron microscopy (SEM) and Brunauer-Emmett-Teller (BET) techniques in order to characterize its structural properties. Hydrogen desorption properties were determined by differential scanning calorimetry (DSC) under nitrogen atmosphere at different heating rates (5, 10, and 15 °C/min). Doyle and Kissenger non-isothermal kinetic models were applied to calculate energy (Ea) values, which were found equal to 254.68 kJ/mol and 255.88 kJ/mol, respectively.

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