p-Xylylenediamine and Its New Polyimides
DOI:
https://doi.org/10.18321/ectj333Abstract
p-Xylylenediamine was synthesized with high yield through a hydrogenization of dinitrile of terephthalic acid. The effect of catalyst and solvent on the yield of the product was studied. The hydrogenization was carried out on skeletal catalysts based on alloy of Reney nickel Ni:Al (1:1) in aliphatic alcohols (C1-C4) at 4.0 MPa and 60 °C. New alkanearomatic polyimides were synthesized by one-step polycondensation of p-xylylenediamine and dianhydride of tricyclodecentetracarboxylic acid in the presence of isonicotinic acid as a catalyst in nonpolar amide solvents at 110-120 °C. The films based on the synthesized polyalkanimides are stable with 70-80 MPa breaking strength and 30-40% elongation. The glass transition temperature of the polymers is within 265-280 °C temperature range, the temperature of decomposition is above 340 °C. The tangent of dielectic loss of the films at 1 kHz and 25 °C is 0.002-0.004, the dielectric permitivity is about 3.22-3.35.
References
(2). Kalugina E.V., Blumenfeld A.B., Novotortsev V.M., Savina M.E. Plastmassy. 3:4 (1996).
(3). Chernova A.G., Savina M.E., Pinaeva N.K. et al. Patent of Russia 93009681/04, 1996.
(4). Zhubanov B.A., Almabekov O.A., Boiko G.I. et al. Vysokomol. Soed. 31A(12):2652 (1989).
(5). Zhubanov B.A., Arkhipova I.A., Almabekov O. A. New thermostable heterocycle polymers. Alma-Ata, Nauka, 1979, p. 252.
(6). Kalinina L.S., Motorina M.A., Nikitina N.I., Khachapuridze N.A. Analysis of condense polymers. Moscow, Chem., 1984, p. 296.
(7). Bradulina L.G., Gavrilova N.D., Vygodskiy Y.S., Matieva A.M. Vysokomol. Soed. 41B(5):901 (1999).
(8). Bizhanova N.B., Abildin T.S., Zhubanov K.A. et al. Izvestia ANKazSSR, Ser. Chem. 4:68 (1981).
(9). Chegolya A.S. Thesis of Ph.D., Moscow, 1968.
(10). Zhubanov B.A. Polymer Yearbook, v.4, 1987, p. 149.
(11). Zhubanov B.A., Kravtsova V.D. Izvestia NAN RK, Ser. Chem. 6:64 (1999).
(12). Nikolskiy B.P. (ed.) Spravochnik Chimica, V.2, Leningrad, Chimia, 1971, p. 1168.
(13). Golodets G.I., Pavlenko N.V., Prokhorenko E.V. Kinetika i kataliz. V. 3, 1987, p. 625.
(14). Freidlin L.K., Sladkova T.A. Uspekhi chimia. 33(6):664 (1964).
(15). Sokolskiy D.V. Hydrogenization in solutions Alma-ata, ANKazSSR. 1962, p. 485.
(16). UK Patent 814631, 1957.
(17). Sheglov N.I., Sokolskiy D.V., Andreeva A.A. et al. Sb. Trudov ICS AN KazSSR, V. 14, 1966, p. 167.
(18). Abildin T.S., Batmanova K.B., Zhubanov K.A. Proc. 5-th Int. Symp.Sciences Turkic Languages Countries on Polymers and Polymer Composites. Almaty, Sept. 6-9, 1999, p. 217.
(19). Bizhanova F.B. Thesis of D.Sc., Alma-Ata, 1976.
(20). Kravtsova V.D., Zhubanov B.A. Proc. KIEEMESummer Annual Confer. Korea, Myongji Univ. Yongin, June 12-16, 2000, V. 1, p. 255.
(21). Zhubanov B.A., Kravtsova V.D. Sb. Mater. Intern. Sci-pract. Confer. ''Chimia: science, education, industry'', Pavlodar, Nov. 15-16, 2001, p. 143.
(22). Voishev V.S., Mikhantiev B.I., Sajin B.I. et al. Vysokomol. Soed. 14B(5):361 (1973).
Downloads
Published
How to Cite
Issue
Section
License
You are free to: Share — copy and redistribute the material in any medium or format. Adapt — remix, transform, and build upon the material for any purpose, even commercially.
Eurasian Chemico-Technological Journal applies a Creative Commons Attribution 4.0 International License to articles and other works we publish.
Subject to the acceptance of the Article for publication in the Eurasian Chemico-Technological Journal, the Author(s) agrees to grant Eurasian Chemico-Technological Journal permission to publish the unpublished and original Article and all associated supplemental material under the Creative Commons Attribution 4.0 International license (CC BY 4.0).
Further distribution of this work must maintain attribution to the author(s) and the published article’s title, journal citation, and DOI.