Novel poly(amide imide)s having inherent viscosities in the range 0.89-1.56 dL/g were prepared by the method of low temperature polycondensation in solution of N,N-dimethylacetamide (DMA) from aromatic diamines and a new monomer: N-[4"-(chloroformylphenyl) -4'-iminobenzoyl] trimellitimide chloride.
Synthesis and characterization of novel benzhydrol-containing poly(amide-imide)s
✍ Scribed by Liaw, Der-Jang; Liaw, Been-Yang; Sillion, Bernard; Mercier, Régis; Thiria, Remi; Sekiguchi, Hikaru
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 96 KB
- Volume
- 48
- Category
- Article
- ISSN
- 0959-8103
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✦ Synopsis
A series of novel benzhydrol-containing poly(amide-imide)s (PAIs) have been prepared from a new diimide-dicarboxylic acid, N,N'-bis(4-hydroxycarbonyl)-benzhydrol-3,3',4,4'-tetracarboxydiimide (BHTDA-DIA), with various diamines by direct polycondensation using triphenyl phosphite and pyridine as condensing agents. The polymers obtained had inherent viscosities of 0.35± 0.96 dl g À1 . All these PAIs, except polymer PAI-2, were soluble in N-methyl-2-pyrrolidinone and N,Ndimethylacetamide containing LiCl (1 wt%). Tough and ¯exible PAI ®lms could be obtained by casting PAIs from their DMAc or NMP solutions, except for polymer PAI-2. The polymer ®lms had a tensile strength of 93±111 MPa, an elongation at break range of 4±6%, and an initial modulus range of 2.7± 3.8 GPa. The glass transition temperatures of most polymers were found to be above 255 °C. These polymers were fairly stable up to a temperature around or above 400 °C, and lost 10% weight in the range 426±507 °C in nitrogen and 423±515 °C in air.
📜 SIMILAR VOLUMES
A series of novel soluble poly(amide-imide)s were prepared from the diimide-dicarboxylic acid, 2,2-bis[N-(4-carboxyphenyl)-phthalimidyl]hexafluoropropane, with various diamines by the direct polycondensation in N-methyl-2-pyrrolidinone containing CaCl 2 using triphenyl phosphite and pyridine as cond
4,4'-(Hexa¯uoroisopropylidene)-bis-(phthalic anhydride) (1) was reacted with L-leucine (2) in toluene solution at re¯uxing temperature in the presence of triethylamine and the resulting imideacid (4) was obtained in quantitative yield. The compound (4) was converted to the diacid chloride (5) by rea