2012
DOI: 10.4028/www.scientific.net/amr.554-556.13
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Study on the Structure and Properties of Polyvinyl Pyrrolidone/ Polyamide 6 Blends

Abstract: 3-10%(wt) Polyvinyl pyrrolidone (PVP) was mixed with PA6 through the twin-screw extruder, a new type of high hygroscopic nylon resins can be obtained. With the increasing addition of PVP the crystalline state of PA6 changes from γ to α phase. The intermolecular hydrogen bond exists between PVP and PA6. The FTIR and WAXD analysis can approve the existence of the intermolecular hydrogen bond and the change of the PA6 crystalline state.

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Cited by 3 publications
(3 citation statements)
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“…Features of interfacial phenomena in polymer blends are determined primarily by the nature of the initial ingredients. 18,19 However, most polymer pairs do not have thermodynamic compatibility. In such blends, the formation of a common crystal lattice is impossible, but we can assume the presence of compatibility between the components based on the formation of common supramolecular structures in the absence of a clear boundary of the transition layers.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…Features of interfacial phenomena in polymer blends are determined primarily by the nature of the initial ingredients. 18,19 However, most polymer pairs do not have thermodynamic compatibility. In such blends, the formation of a common crystal lattice is impossible, but we can assume the presence of compatibility between the components based on the formation of common supramolecular structures in the absence of a clear boundary of the transition layers.…”
Section: Resultsmentioning
confidence: 99%
“…Thermal annealing has a different effect: for polystyrene-based samples an accelerated relaxation and reduction of internal stresses are observed; for polyamide recrystallization and an increase in the crystallinity degree are obvious. 18 Along with the physicomechanical properties of thermoplastic -PVP blends, we studied the effect of PVP content on their thermophysical parameters, in particular the Vicat softening point (Fig. 10).…”
Section: Resultsmentioning
confidence: 99%
“…For stretching vibration, the formation of hydrogen bonds generally increases the bond length and decreases the bond energy, leading to a stronger absorption intensity and lower wavenumber. [49][50][51] Hence, the downshifted wavenumber revealed that intermolecular hydrogen bonds were formed between the C = O bond in PVP and C─OH bond in SWCNTs. Actually, there are lone pair electrons in oxygen and nitrogen atoms of the amide bonds in PVP molecular, both of which can form hydrogen bonds.…”
Section: Illustration Of Mechanismmentioning
confidence: 97%