Abstract
A series of polyamides and poly(amide-imide)s were prepared by the direct polycondensation of 4,4′-[sulfonylbis(1,4-phenyleneoxy)]dianiline or 4,4′-[sulfonylbis(2,6-dimethyl-1,4-phenyleneoxy)]dianiline with aromatic dicarboxylic acids and phthalimide unit-bearing dicarboxylic acids in a N-methyl-2-pyrrolidone (NMP) solution containing dissolved calcium chloride using triphenyl phosphite and pyridine as condensing agents. The inherent viscosities of the resulting polymers were above 0.45 dL/g and up to 1.70 dL/g. Except for the polyamides derived from terephthalic acid and 4,4′-biphenyldicarboxylic acid, all the other polyamides and all poly(amide-imide)s were readily soluble in polar organic solvents such as NMP, N, N-dimethylacetamide (DMAc), N,N-dimethylformamide (DMF), dimethyl sulfoxide (DMSO), and m-cresol, and afforded transparent and tough films by solution-casting. Most of the polymers showed distinct glass transition on their differential scanning calorimetry (DSC) traces and their glass transition temperatures (Tg) stayed between 140–264 °C. The methyl-substituted polymers showed higher Tgs than the corresponding unsubstituted counterparts. The results of the thermogravimetry analysis (TGA) revealed that all the methyl-substituted polymers showed lower initial decomposition temperatures than the unsubstituted ones.
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References
P. E. Cassidy, Thermally Stable Polymers, Dekker, New York, 1980.
H. H. Yang, Aromatic High-Strength Fibers, Wiley, New York, 1989.
S.-H. Hsiao and C.-P. Yang, J. Polym. Sci., Polym. Chem., 28, 2501 (1990).
H. Manami, M. Nakazawa, Y. Oishi, M. Kakimoto and Y. Imai, J. Polym. Sci., Polym. Chem., 28, 465 (1990).
C.-P. Yang and W.-T. Chen, Makromol. Chem., 193, 2323 (1991).
C.-P. Yang and J.-H. Lin, J. Polym. Sci., Polym. Chem., 31, 2153 (1993).
C. Chiriac and J. K. Stille, Macromolecules, 10, 712 (1977).
G. L. Brode, G. T. Kwiatkovski and A. W. Bedwin, J. Polym. Sci., Polym. Chem. Ed., 12, 575 (1974).
J. Adduci, L. L. Chapoy, G. Jonsson, J. Kops and B. M. Shinde, J. Appl. Polym. Sci., 28, 2069 (1983).
S. B. Idage, B. M. Shinde and S. P. Vernekar, J. Polym. Sci., Polym. Chem., 27, 583 (1989).
N. Avella, G. Maglio, R. Palumbo, F. Russo and M. C. Vignola, Makromol. Chem., Rapid Commun., 14, 545 (1993).
M. Bruma, F. Mercer, J. Fitch and P. Cassidy, J. Appl. Polym. Sci., 56, 527 (1995).
D. M. Stoakley, A. K. St. Clair and C. I. Crolla, J. Appl. Polym. Sci., 51, 1479 (1994).
Y. Delaviz, A. Gungor, J. E. McGrath and H. W. Gilson, Polymer, 34, 210 (1993).
F. Keitoku, M. Kakimoto and Y. Imai, J. Polym. Sci., Polym. Chem., 32, 317 (1994).
S.-H. Hsiao and P.-C. Huang, J. Polym. Sci., Polym. Chem., 35, 2421 (1997).
S.-H. Hsiao and P.-C. Huang, Macromol. Chem. Phys., 198, 4001 (1997).
J. S. McHattie, W. J. Koros and D. R. Paul, Polymer, 32, 840 (1991); (b) J. S. McHattie, W. J. Koros and D. R. Paul, Polymer, 33, 1701 (1992); (c) C. L. Aitkeu, W. J. Koros and D. R. Paul, Macromolecules, 25, 3651 (1992).
S.-H. Hsiao, C.-P. Yang and C.-K. Lin, J. Polym. Res., 2, 1 (1995).
S.-H. Hsiao and C.-P. Yang, J. Polym. Sci., Polym. Chem., 28, 1149 (1990).
S.-H. Hsiao, C.-P. Yang and F.-Y. Wu, J. Polym. Sci., Polym. Chem., 32, 1481 (1994).
S.-H. Hsiao and C.-P. Yang, Makromol. Chem., 191, 155 (1990).
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Hsiao, SH., Yang, CP. & Li, CT. Synthesis and characterization of polyamides and poly(amide-imide)s based on ether-sulfone-diamines. J Polym Res 5, 243–248 (1998). https://doi.org/10.1007/s10965-006-0063-6
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DOI: https://doi.org/10.1007/s10965-006-0063-6