TANSO
Online ISSN : 1884-5495
Print ISSN : 0371-5345
ISSN-L : 0371-5345
Volume 1979, Issue 99
Displaying 1-2 of 2 articles from this issue
  • Tetsuo Murata, Yoshiharu Matsuda
    1979 Volume 1979 Issue 99 Pages 125-129
    Published: October 25, 1979
    Released on J-STAGE: June 28, 2010
    JOURNAL FREE ACCESS
    The ζ-potential of carbon black particles was studied in connection with their dispersion.The influences of the quinone group on the surface, the position of the slipping plane, which controlled the surface charge density, and the temperature of measurement on the ζ-potential of carbon black particles were investigated.A carbon black for rubber and their oxidized ones were used.The ζ-potential was determined by the measurement of electrophoretic migration of the carbon black particles in aqueous solutions of alkali-metal chlorides and by the calculation with Hiickel's equation.The ζ-potential with negative value was induced by the selective adsorption of Cl-anions and dissociation reaction of acidic groups on the surface of the carbon black particles.The absolute value of the ζ-potential was the higher for the carbon black particles with the more amount of acidic groups.In the sample with high concentration of quinone group, the reactivity of the quinone group was determined the value of ζ-potential.The influence of alkali-metal cations at the same concentration on the absolute value of the ζ-potential was the order of Li+<Na+<K+<Rb+.This order changed with the surface charge density and the position of the slipping plane.The absolute value of the ζ-potential increased by elevating temperature.
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  • M. Inagaki, M. Endo, A. Oberlin, S. Kimura, M. Nakamizo, Y. Hishiyama, ...
    1979 Volume 1979 Issue 99 Pages 130-137
    Published: October 25, 1979
    Released on J-STAGE: June 28, 2010
    JOURNAL FREE ACCESS
    The structure of one of mesophase pitch-based carbon fibers with random cross sectional texture was studied by various techniques;X-ray diffraction, magnetoresistance, laser Raman spectroscopy, high resolution electron microscopy, electron diffraction from periphery of the fiber, polarized light microscopy and scanning electron microscopy.
    The fibers used were prepared from the mesophase pitch by spinning at370°C, oxidizing at 325°C and then heating up to 900°C (Ref.2).Their diameter was about20 μm and the density was 1.74g/cm3. The fibers were heattreated at 3000°C for 30 min in the flow of argon.They were also heattreated at different temperatures, 1600°, 2000°, 2500°, for about 10 sec in order to know the process of structural change.
    The results of X-ray diffraction, magnetoresistance and laser Raman spectroscopy were summarized in Table1.The interlayer spacing d002 decreased with the increase in heat treatment temperature, but the growth of apparent thickness of crystallite Lc was restrained.The positive value of maximum transverse magnetoresistance (Δρ/ρ) max and small value of intensity ratio R of 1360cm-1 line to 1580cm-1 line indicated relatively high degree of graphitization of the fiber heat-treated at 3000°C.The value of anisotropy factor A close to 1 and small values of half-maximum width of the orientation function ψ1/2 which were determined both from X-ray diffraction and magnetoresistance measurement revealed the remarkable orientation of crystallites along the fiber axis.On the 3000°C-treated fiber, crystallite orientation in the cross section was observed (Fig.1c, T arrangement) and it seemed to be related to the deformation of the cross section of the fiber (Fig.6).The relations between d002 and Lc, and also between (Δρ/ρ) max and R did not coincide with those found on various cokes, that might be due to some constraint from the fibrous shape.
    Under electron microscope, well-developed graphite lamellae with wrinkles were found, their microtexture being clarified by dark-field image technique and electron diffraction (Fig .2).In the fibers heat-treated at low temperatures, the porous regions with small and randomly-oriented layers coexisted with the regions with well-developed layers (Figs .3 and 4), the former being hard-carbon-like and the latter soft-carbon-like in the microtexture and its change with heat treatment.
    The different values of R were obtained for the single fiber and for its powdered sample (Table 1).It means a heterogeneity in the graphitization degree.On the 2500°C-treated fiber, the value of single fiber was 0.18 and it increased to 0.30, close to the value for the powdered, after the oxidation in air at500°C for about5h (15% weight loss). These experimental results suggest that the periphery of the fiber has higher degree of graphitization than the interior.From polarized light microscopy, the units for optical anisotropy (mosaic units) were found to be smaller in the periphery than in the interior.
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