1994
DOI: 10.1002/pola.1994.080321111
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Synthesis and properties of poly(arylene ether phenyl‐s‐triazine)s

Abstract: A series of new poly(arylene ether phenyl‐s‐triazine)s was prepared by the nucleophilic aromatic substitution polymerization of the potassium salt of bisphenols with 2,4‐bis (halophenyl)‐6‐phenyl‐s‐triazine in N‐methyl‐2‐pyrrolidone at elevated temperature. The polymers with inherent viscosities exceeding 0.5 were obtained after polymerization for 1 h using 2,4‐bis(fluorophenyl)‐6‐phenyl‐s‐triazine as a monomer. The glass transition temperatures of the resulting polymers ranged from 200 to 260°C depending on t… Show more

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Cited by 23 publications
(16 citation statements)
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“…Despite these properties, it has been reported to be immiscible or partially miscible with most polymers, even with acrylic polymers. [2][3][4] For this reason, we wanted to find miscible polymer blends based on PVA and to illustrate the effect of high-energy radiation on the structure-property behavior of these blends. In this regard, PVA/carboxymethyl cellulose (CMC) water-soluble polymer blends were used as sorbents for dye wastes.…”
Section: Introductionmentioning
confidence: 99%
“…Despite these properties, it has been reported to be immiscible or partially miscible with most polymers, even with acrylic polymers. [2][3][4] For this reason, we wanted to find miscible polymer blends based on PVA and to illustrate the effect of high-energy radiation on the structure-property behavior of these blends. In this regard, PVA/carboxymethyl cellulose (CMC) water-soluble polymer blends were used as sorbents for dye wastes.…”
Section: Introductionmentioning
confidence: 99%
“…Depending on their chemical structure and thermal behavior, phenyl-s-triazine polymers may exist as a thermal plastic or as a thermosetting material [10,11]. As a class of new emerged thermal plastics, poly(aryl ether phenyl-s-triazine)s (PAEPs) are generally amorphous or semi-crystalline polymers with T g s exceeding 240°C as well as acceptable mechanical properties and good chemical resistance [12][13][14][15][16][17]. PAEPs are normally thought of as one of the most thermally stable polyethers.…”
Section: Introductionmentioning
confidence: 99%
“…[1][2][3][4][5][6][7] tion of flexibilizing groups and bulky units in the polymer backbone. [8][9][10][11][12][13][14][15][16][17][18][19][20][21] Solubility, glass transition Drawbacks of these polymers are their insolubility and intractability, which cause difficulties in temperature, and crystallinity can be adjusted by varying the nature of aromatic ring systems and the number of flexible linkages within the poly-2,2-bis(3,4-dicarboxyphenyl)hexafluoropropane dianhydride (6FDA; 4f, Chriskev) were used as received. Pyromellitic dianhydride (PMDA; 4a, Aldrich) and 3,3,4,4-benzophenonetetracarboxylic dianhydride (BTDA; 4d, Aldrich) were recrystallized from acetic anhydride prior to use.…”
Section: Introductionmentioning
confidence: 99%
“…The solution was continuously stirred at 6.47-6.78 ppm (aromatic protons). 13 b Measured at a concentration of 0.5 g/dL in DMAc-5% LiCl at 30ЊC using a Cannon-Fenske viscometer. c ''2.0 / 1.0'' means that an initial amount of 2 mL was used and additional amount of 1 mL was added when the reaction medium was too viscous to stir.…”
Section: Introductionmentioning
confidence: 99%