Journal of The Adhesion Society of Japan
Online ISSN : 2187-4816
Print ISSN : 0916-4812
ISSN-L : 0916-4812
Volume 57, Issue 4
Displaying 1-4 of 4 articles from this issue
Review
Original Paper
  • Aoi OISHI, Takashi TANAKA
    2021Volume 57Issue 4 Pages 145-151
    Published: April 01, 2021
    Released on J-STAGE: October 23, 2024
    JOURNAL FREE ACCESS

    This study investigated a nondestructive imaging method for morphological characterization of adhesive

    bondlines in wood-based materials using X-ray micro-computed tomography( CT). Softwood and hardwood

    plywood were prepared using phenol-formaldehyde resin adhesive( PF); hardwood glulam was prepared using

    water-based polymer-isocyanate adhesive. These materials were scanned using six industrial X-ray CT apparatuses.

    Each resulting scan was reconstructed into three-dimensional grayscale voxel data and saved as a

    stack of grayscale slice images. In softwood plywood images with field of view( FOV) of approximately 30 mm

    diameter, tracheids and PF resin in tracheid lumen but were not clearly visualized. In contrast, in softwood

    plywood images with FOV of 3.6 mm diameter, tracheids and PF resin in tracheid lumen were clearly visualized.

    In hardwood plywood images with FOV of 3.6 mm diameter, PF resin in vessels and its crack were clearly

    visualized, probably owing to resin shrinkage during solidification in the vessels. In hardwood glulam images

    with FOV of 0.8 mm diameter, resin at the bondline and its internal heterogeneity were visualized. The developed

    method realizes morphological observations in wood-based materials with FOV of several mm diameter

    and can be applied to a wide variety of wood adhesion studies such as the investigation of the effects of morphological

    characteristics on material strengths.

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Original Paper
  • Takeshi KAKARA, Atsushi IZUMI, Tomoyuki KOGANEZAWA
    2021Volume 57Issue 4 Pages 139-144
    Published: April 01, 2021
    Released on J-STAGE: October 23, 2024
    JOURNAL FREE ACCESS

    In situ analysis of the residual stress in a glass fiber-reinforced resole-type phenolic resin and aluminum

    foil composite material during curing and thermal-cycle testing was performed via X-ray diffraction

    measurements of Al(422)-plane using the sin2 Ψ method. In the curing process, the residual stress at the

    resin and aluminum interface changed due to the difference in the magnitude of the thermal expansion and

    contraction between them, which arose by the difference in the coefficient of the thermal expansion( CTE),

    and a cure-shrinkage of the resin. Additionally, the behavior of the stress change was greatly influenced by the

    glass-transition of the resin which involved a large CTE change of the resin. The stress-free temperature was

    successfully determined by the stress-change during the thermal cycle, in which the resin-aluminum interface

    in the investigated composite was in a stress-free state at 160 ℃. The continuous stress change during curing

    showed that the residual stress in the cured composite was strongly affected by the stress state before curing,

    suggesting that the stress-free temperature could be controlled by the composite molding process.

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Comprehensive Paper
  • Kensuke NAKA
    2021Volume 57Issue 4 Pages 128-138
    Published: April 01, 2021
    Released on J-STAGE: October 23, 2024
    JOURNAL FREE ACCESS

    This report focuses on recent efforts to prepare single component element-block materials based on cage

    silsesquioxane frameworks. Polyhedral octasilsesquioxanes (POSSs), denoted as (RSiO1.5)8 or labeled T8 cages

    are used here as the cage silsesquioxane frameworks. Thermoplastic optically transparent silsesquioxane materials

    derived from a single cage compound can be achieved by dumbbell- and star-shaped cage structures,

    allowing precise design their structures for tuning properties. Incompletely condensed POSS exhibited lower

    crystallinity without loss of thermal stability in comparison with a completely condensed POSS. Di-functional

    POSS monomers, which were prepared by a selective corner-opening reaction and a subsequent corner-capping

    reaction, significantly reduce their crystallinity in comparison with those of mono-functionalized T8 cages.

    Several examples for polymerization of the di-functional POSS monomers are described.

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