2000
DOI: 10.1002/1099-1581(200007)11:7<359::aid-pat980>3.0.co;2-k
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Shrinkability of ethylene vinyl acetate/polyurethane blends and their characterization

Abstract: Heat shrinkability of the polymer, which depends on the elastic memory, is being utilized in various applications, mainly in the field of encapsulation. The elastic memory is introduced into the system in the form of an elastomeric phase. Here the blends of ethylene vinyl acetate and polyurethane were studied with reference to their shrinkability, introducing crosslinking in both the phases. It is found that with increase in elastomer content the shrinkage increased to a certain level and then decreased. With … Show more

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Cited by 12 publications
(9 citation statements)
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“…10 For pure LDPE and LE73 blends in presence and absence of clay, peak positions of polymer crystals and half width remained unchanged, which led to the conclusion that crystal type and crystallite sizes were unchanged. 16,17 Total amount of crystallinity was also almost same. After irradiation at 100 kGy doses there was no change of crystallinity and crystal type.…”
Section: Resultsmentioning
confidence: 60%
“…10 For pure LDPE and LE73 blends in presence and absence of clay, peak positions of polymer crystals and half width remained unchanged, which led to the conclusion that crystal type and crystallite sizes were unchanged. 16,17 Total amount of crystallinity was also almost same. After irradiation at 100 kGy doses there was no change of crystallinity and crystal type.…”
Section: Resultsmentioning
confidence: 60%
“…The d ‐space, crystallite size ( P ), and interchain distance ( r ) of neat, unirradiated, and irradiated blends and composites are calculated as follows d=λ2 normalsnormalinormalnθ P=K λB normalcnormalonormalsθ R=5 λ8 normalsnormalinormalnθ where K is considered here as 0.90 and λ is 1.54 Å wavelength of Cu X‐ray source.…”
Section: Methodsmentioning
confidence: 99%
“…X-ray diffraction was performed with a PW 1840 X-ray Diffractometer with a copper target (Cu-K a ) at a scanning rate of 0.05 2h=sec., chart speed 10 mm=2h, range 5000 c=s, and a slit of 0.2 mm, applying 40 kV, 20 mA, to assess the change in crystallinity of the blends as a function of blend ratio [14,15] . Differential scanning calorimetry (DSC) was carried out using a Perkin-Elmer PYRIS Diamond DSC instrument in presence of nitrogen, in the temperature range 50-600 C. Thermo gravimetric analysis (TGA) was carried out using Universal TGA-2950 TA instrument in the temperature range 20-700 C. Dynamic fracture mechanism of the blends were studied by scanning electron microscope (SEM) (JSM-5800 of JEOL Co.), after auto sputter coating of the fractured surface with gold at 0 felt angle.…”
Section: Methodsmentioning
confidence: 99%