2015
DOI: 10.3144/expresspolymlett.2015.21
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Effect of the solvent type and polymerization conditions on the curing kinetics, thermal and viscoelastic performance of poly(amide-imide) resins

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Cited by 10 publications
(8 citation statements)
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“…The peaks of the phenyl protons of the ISBA, PMDA, and BPDA units appear in the upfield region of 7.7–8.4 ppm, and the peaks of CH and CH 2 of the alicyclic ring in the ISBA and CBDA units appear in the downfield region of 3.6–5.4 ppm. The characteristic signals of the C–H group in CBDA are observed for shifting in signal of peak 7, attributed to the two forms of isomers with different steric structures . The minor peaks at 6.6 and 7.8–7.9 ppm would be assigned to the aromatic protons of the end groups of polymers, such as the p -aminophenyl groups.…”
Section: Resultsmentioning
confidence: 99%
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“…The peaks of the phenyl protons of the ISBA, PMDA, and BPDA units appear in the upfield region of 7.7–8.4 ppm, and the peaks of CH and CH 2 of the alicyclic ring in the ISBA and CBDA units appear in the downfield region of 3.6–5.4 ppm. The characteristic signals of the C–H group in CBDA are observed for shifting in signal of peak 7, attributed to the two forms of isomers with different steric structures . The minor peaks at 6.6 and 7.8–7.9 ppm would be assigned to the aromatic protons of the end groups of polymers, such as the p -aminophenyl groups.…”
Section: Resultsmentioning
confidence: 99%
“…The characteristic signals of the C−H group in CBDA are observed for shifting in signal of peak 7, attributed to the two forms of isomers with different steric structures. 38 The minor peaks at 6.6 and 7.8−7.9 ppm would be assigned to the aromatic protons of the end groups of polymers, such as the paminophenyl groups. Note that the alicyclic rings of ISBA and CBDA were derived from biosources ISB and maleic acid, respectively.…”
Section: Synthesis Of Co-pi Pi(isba-cmbn)mentioning
confidence: 99%
“…In addition, the absorptions at 2210 cm −1 , attributed to the carbon-carbon stretching vibrations in phenylethynyl groups (-C≡C-), were not disappeared even after being thermally treated at 260 °C, implying that no obvious thermal curing reaction occurred [ 39 ]. The characteristic peaks of isoimide around 1800 cm −1 and 905 cm −1 were not detected, implying that the imidization process didn’t produce the corresponding isoimide groups [ 40 ]. Figure 3 b compares the FT-IR spectra of the thermally cured blend resin (TMR–50/RDm–a–5) with the thermosetting matrix resin (TMR–50) and the reactive diluent (RDm–a) after cured at 380 °C/2 h. Obviously, the thermally cured TMR–50/RDm–a–5 exhibited the expected chemical structures.…”
Section: Resultsmentioning
confidence: 99%
“…Figure 1 d plots the DSC–TGA curves of the precursor. As seen, the endothermic peaks at around 202 and 87 °C are, respectively, attributed to the evaporation of NMP and water from Cu(NO 3 ) 2 ·3H 2 O [ 25 , 26 ], while the exothermic peak at around 212 °C is related to the decomposition of Cu(NO 3 ) 2 [ 26 ]. Importantly, the peaks at around 180 °C (with a range from 140 to 200 °C) is identified in the DSC curve, which agrees to the decomposition temperature of EG [ 27 , 28 ].…”
Section: Resultsmentioning
confidence: 99%