2011
DOI: 10.1002/app.34416
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Synthesis and thermal decomposition of poly(dodecamethylene terephthalamide)

Abstract: A kind of semiaromatic polyamide, poly(dodecamethylene terephthalamide) (PA12T) was synthesized via a polycondensation reaction of terephthalic acid and 1,12-dodecanediamine. The structure of prepared PA12T was characterized by Fourier transform infrared spectroscopy, proton nuclear magnetic resonance ( 1 H-NMR), and elemental analysis. The mechanical properties of PA12T were also studied. The thermal behavior of PA12T was determined by differential scanning calorimetry, thermogravimetric analysis, and dynamic… Show more

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Cited by 32 publications
(21 citation statements)
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“…FTIR spectra of PA10T/1012 samples with different 1012 contents are shown in Figure . The characteristic peaks of amide groups are found: the peaks at 3309 cm −1 are due to the NH stretching vibration, the sharp peaks at 1622 cm −1 are attributed to the CO stretching vibration (amide I), another sharp peaks at 1537 cm −1 are assigned to the CN stretching and CONH bending vibration (amide II), the peaks at 1290 cm −1 are assigned to the CN stretching and CH bending vibration (amide III), the peaks at 637 cm −1 are assigned to the NH in‐plane bending vibration (amide V), and the weak peaks at 3074 cm −1 are attributed to the overtone of the NH bending vibration. Because the chemical structure of PA10T/1012 is similar to PA10T homopolymer, they have same characteristic vibration bands in FTIR spectra.…”
Section: Resultsmentioning
confidence: 99%
“…FTIR spectra of PA10T/1012 samples with different 1012 contents are shown in Figure . The characteristic peaks of amide groups are found: the peaks at 3309 cm −1 are due to the NH stretching vibration, the sharp peaks at 1622 cm −1 are attributed to the CO stretching vibration (amide I), another sharp peaks at 1537 cm −1 are assigned to the CN stretching and CONH bending vibration (amide II), the peaks at 1290 cm −1 are assigned to the CN stretching and CH bending vibration (amide III), the peaks at 637 cm −1 are assigned to the NH in‐plane bending vibration (amide V), and the weak peaks at 3074 cm −1 are attributed to the overtone of the NH bending vibration. Because the chemical structure of PA10T/1012 is similar to PA10T homopolymer, they have same characteristic vibration bands in FTIR spectra.…”
Section: Resultsmentioning
confidence: 99%
“…The band at 3308 cm −1 is assigned to hydrogen bond and ν N–H in polyamide. The bands at 1622, 1537, 1495, 1288 and 637 cm −1 are assigned to amide Ⅰ ( ν C=O ), amide Ⅱ ( ν C–N and δ N–H ), amide Ⅲ ( ν C–N and δ C–H ), amide Ⅳ ( ν C–CO ) and amide Ⅴ ( δ N–H ), respectively [ 34 ]. And the intensity of these bands decrease with the content of 1014 units increasing, which attributed to the longer molecular chain of 1,12-dodecanedicarboxylic acid compared with terephthalic acid so that the amide bonds density of PA10T/1014 is lower than PA10T.…”
Section: Resultsmentioning
confidence: 99%
“…The coupled absorption band at 2857 (symmetric) and 2952 cm −1 (asymmetric) are attributed to the stretching vibration of V C–H . The signals at 1630, 1536, 1460, 1255, and 686 cm −1 are attributed to amide-I (V C=O ), amide-II (V C –N stretch and V N –H band), amide-III (V C–N and δ C–H ), amide-IV (V C–C=O ), and amide-V (V N–H , out-of-plane bonding vibration), respectively [37]. Nonetheless, for the copolyamides with an increasing weight ratio of BABT/SA, these amide absorption bands appeared weaker, which denotes a reduction in the crystallinity order.…”
Section: Resultsmentioning
confidence: 99%