2013
DOI: 10.1002/app.39312
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Crosslinking behavior of polyarylene ether nitrile terminated with phthalonitrile (PEN‐t‐Ph)/1,3,5‐Tri‐(3,4‐dicyanophenoxy) benzene (TPh) system and its enhanced thermal stability

Abstract: A novel polyarylene ether nitrile terminated with phthalonitrile (PEN-t-Ph) was synthesized by a simple solution polycondensation of biphenyl and hydroquinone with 2,6-dichlorobenzonitrile, followed by termination with 4-nitrophthalonitrile. The PENt-Ph/1,3,5-Tri-(3,4-dicyanophenoxy) benzene (TPh) system was prepared by cure treatment. The phthalonitrile on PEN-t-Ph were thermally crosslinked with TPh in the presence of diamino diphenyl sulfone through cure treatment up to 280-340 C, which led to the transform… Show more

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Cited by 34 publications
(33 citation statements)
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“…The polyarylene ether nitrile terminated with phthalonitrile (PEN-Ph) is firstly synthesized in our laboratory according to our previous work35. Through simply curing with high temperature, the phthalonitriles capped at the ends of PEN self-crosslink and form the phthalocyanines as the crosslinking points in the system3637. As the crosslinking points are at the ends of linear PEN, the obtained network is a PEN elastomer.…”
Section: Resultsmentioning
confidence: 99%
“…The polyarylene ether nitrile terminated with phthalonitrile (PEN-Ph) is firstly synthesized in our laboratory according to our previous work35. Through simply curing with high temperature, the phthalonitriles capped at the ends of PEN self-crosslink and form the phthalocyanines as the crosslinking points in the system3637. As the crosslinking points are at the ends of linear PEN, the obtained network is a PEN elastomer.…”
Section: Resultsmentioning
confidence: 99%
“…It is well known that phthalonitrile shows excellent reactivity and crosslinkable property [19,20]. Therefore, by introducing the phthalonitrile in the end of the PEN main chain, the PEN-Ph integrated the excellent performances of PEN [21][22][23][24][25] (high thermal stability, superior mechanical properties as well as good workability) and the crosslinkable property of the phthalonitrile, resulting in more excellent thermal properties and mechanical properties [26,27]. Besides, the PEN-Ph also possesses partially crystalline owing to the regular structure of the part of the molecular chain.…”
Section: Introductionmentioning
confidence: 99%
“…Compared with the phthalonitrile resins reported, stronger endothermic peaks below 300 °C were observed after blending the resins with the mixed curing agent, as seen in Figure , suggesting obvious curing reactions were occurring as a result of the enhanced moveability of the chain segments. The curing peak temperature was reduced after BP‐Ph was added, implying higher curing reactivity was obtained.…”
Section: Resultsmentioning
confidence: 86%