• Journal of Welding and Joining
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• v.9 no.1
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• pp.48-57
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• 1991

Welding of dissimilar materials is an area of growing importance in the automotive, aerospace, electronics medical and other domestic appliance industries. This study investigated the ultrasonic welding of dissimilar polymers. Two amorphous and two semicrystalline polymers were used, utilizing all possible welding combinations. For each combination of dissimilar materials, the weldabilitys of the joint was evaluated as a function of weld time, amplitude of vibration and pressure. The joint was also examined microscopically to analyze the melting and flow of the materials. It was generally around found that welding of amorphus polymers resulted in very poor joints. Welding of the amorphous polymers together and welding of the semicrystalline polymers together produced good joints.

• Macromolecular Research
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• v.9 no.4
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• pp.228-237
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• 2001

The evolution of conformational constraints in bisphenol-A polycarbonate (BAPC) upon quiescent bulk crystallization was quantitatively analyzed from calorimetric study employing a rigid amorphous fraction (RAF) as an indicator of the level of conformational constraints. From the correlation between corrected crystallinity (X$\sub$c/) and total rigid fraction (f$\sub$r/), it was found that, regardless of molar mass distribution and thermal treatment conditions, semicrystalline BAPC always exhibits greater f$\sub$r/ than X$\sub$c/ maintaining a quantitative relationship of f$\sub$r/〓2X$\sub$c/ in the range of 0.0 $\sub$c/< 0.4. This directly indicates the evolution of approximately the same amount of RAF as X$\sub$c/, (i.e., RAF〓X$\sub$c/) upon bulk crystallization of BAPC. It was also found that T$\sub$g/ per se and T$\sub$g/ broadening enhance as RAF increases, and there appears to be a critical level of RAF (>0.2) needed to initiate significant changes in both quantities.

• Journal of the Korean Society for Precision Engineering
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• v.9 no.1
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• pp.118-125
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• 1992

Joining of thermoplastics is an area of growing importance in the automotive, aerospace, electronics medical and other domestic appliance industries. While adhesive Bonding or mechanical fastening could be used to join thermoplastics, welding is very effective because of its speed and low cost. This study investgated the ultrasonic joining of thermoplastics. Four kinds of thermoplastics such as Acrylonitrile Butadiene Styrene, Polystyrene, Polyethylene and Polypropylene were used, ultilizing all possible joining combinations. In each combination of thermoplastics, the weldability of the joint was evaluated as a function of weld time, amplitude of vibration and pressure. It was generally found that joining of amorphous thermoplastics with semicrystalline thermopastics resulted in poor joints due to its different crystalline structure. Joining of the amorphous thermoplastics together and joining of the semicrystalline thermoplastics together produced the best joints owing to its same crystalline structure.

• Proceedings of the Korean Fiber Society Conference
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• 1987.06a
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• pp.14-14
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• 1987

• Proceedings of the Korean Fiber Society Conference
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• 1998.04a
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• pp.54-57
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• 1998

Recently, Manley's group published several papers on the blend of PVDF and poly(1, 4-butylene adipate) (PBA) chosen as a model system of somicrystallineisemicrystalline polymer blend.[1-4]. This blend system has several advantages over the other PVDF/semicrystalline polymer blends.(omitted)

• Proceedings of the Korean Fiber Society Conference
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• 1998.10a
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• pp.199-202
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• 1998

Random copolymers are widely used as materials since they afford a convenient possibility of adjusting properties through the compositions of the copolymers. In the case of semicrystalline polymers, the degree of crystallinity generally decreases as the content of the minor component increases, leading often to fully amorphous materials even at low concentrations of the comonomer. (omitted)

• Proceedings of the Korean Fiber Society Conference
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• 2003.10b
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• pp.52-54
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• 2003

Poly(vinyl alcohol) (PVA) obtained by the saponification of poly(vinyl ester) is a linear semicrystalline polymer; these polymers have been widely used as fibers for clothes and industries, binders, films, membranes, medicines for drug delivery system, and cancer cell-killing embolic materials. PVA fibers have high tensile and compressive strength, tensile modulus, and abrasion resistance because of the highest crystalline lattice modulus. (omitted)

• Proceedings of the Korean Fiber Society Conference
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• 2003.10b
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• pp.181-182
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• 2003

Poly(vinyl alcohol) (PVA) is a semicrystalline polymer whose hydroxyl groups produce inter-and intramolecular hydrogen bonding. The extent of hydrogen bonding is greatly affected by stereoregularity of hydroxyl groups, so-called tacticity, of PVA[1-3]. Hydrogen bonding has a profound effect on the rheological and mechanical properties of the polymer, which is largely determined by the density and spatial arrangement of hydroxyl groups. (omitted)

• Proceedings of the Korean Fiber Society Conference
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• 2001.10a
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• pp.432-435
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• 2001

Polymer/clay nanocomposites have received much attention in recent years, because they often exhibit physical properties that are dramatically different from those observed in their micro- and rnacrocornposite counterparts. The presence of clay may affect the crystallization behavior of semicrystalline polymer. (omitted)

• Elastomers and Composites
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• v.42 no.4
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• pp.217-223
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• 2007

Thermomechanical and shape memory properties of dicumyl peroxide(DCP) cured semicrystalline EPDM($Nordel^{(R)}$ IP) were investigated. From gel content analysis, it can be seen that Nordel can be crosslinked by small amount of DCP and the degree of crosslinking increased with the increase of DCP content. DSC analysis revealed that the melting temperature and degree of crystallinity of the crosslinked rubber decreased with the increase of DCP. Tensile test showed that tensile modulus increased and elongation at break of the rubber decreased with an increase in the degree of cross linking. The chemically crosslinked semi-crystalline EPDM exhibited excellent shape memory behavior, i.e. the sample was easily deformed to have an arbitrary secondary shape above its melting temperature and was fixed well in its deformed state when it is cooled, and then the fixed shape was recovered to its original shape very fast upon heating above its melting temperature.