2011
DOI: 10.1002/app.34534
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Investigation of melting behaviors and crystallinity of linear polyamide with high‐aliphatic content

Abstract: ABSTRACT:The melting behaviors and crystal structures of a long alkyl chain polyamide and nylon 18 18, were investigated under annealing and isothermal crystallization conditions. Nylon 18 18 showed multiple melting peaks in differential scanning calorimetry (DSC) thermograms depending on thermal history of the samples. The origin of the multiple melting peaks may be a result of a melting and recrystallization mechanism during DSC scans. Wide-angle X-ray diffraction patterns showed two new diffraction peaks, w… Show more

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Cited by 15 publications
(15 citation statements)
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“…[54] Stoichiometric amountso ft he diamine and the diacid were reactedi nt he initial presence of excesswater as ar eaction medium (Table 2). [54] Stoichiometric amountso ft he diamine and the diacid were reactedi nt he initial presence of excesswater as ar eaction medium (Table 2).…”
Section: Polycondensationmentioning
confidence: 99%
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“…[54] Stoichiometric amountso ft he diamine and the diacid were reactedi nt he initial presence of excesswater as ar eaction medium (Table 2). [54] Stoichiometric amountso ft he diamine and the diacid were reactedi nt he initial presence of excesswater as ar eaction medium (Table 2).…”
Section: Polycondensationmentioning
confidence: 99%
“…Melt-polycondensations were carriedo ut under elevated pressure in a2 5mLs tainless steel reactor. [54] Stoichiometric amountso ft he diamine and the diacid were reactedi nt he initial presence of excesswater as ar eaction medium (Table 2).…”
Section: Polycondensationmentioning
confidence: 99%
See 1 more Smart Citation
“…The results show that the untreated sample, which is the same as a semi crystalline polymer structure, presented some large and wide reflections due to its internal structure, and can be assigned according to the literature [17][18][19], with one significant peak appearing Figure 2, when the heat-setting condition surpassed C1, two peaks appeared that were (002) and (100). As the temperature increased, (002) peaks shifted from 19.58°t o 22.58°, then the (100) diffraction peaks enhance.…”
Section: Crystallinity Studymentioning
confidence: 67%
“…Peaks were assigned according to lit. 42,43 Considering the low sensitivity of 13 C-NMR, terminal carboxylic acid group with higher concentration was chosen to be a reference to determine the concentration of phenyl groups deduced from benzoic acid. Terephthalic end groups (Tx) appeared at 133.27, 130.68, and 127.38 ppm, and benzoic end groups (Bx) appeared at 135.…”
Section: Articlementioning
confidence: 99%