Development of Methods for the Synthesis of Bis-(N-Maleimide)aryl and Bis-Diallyl Bisphenol Monomers for Thermosetting Polymers
- Autores: Kudryashova E.S.1, Otvagin V.F.1, Romanov K.A.1, Afanasyeva E.S.2, Morozov O.S.2, Babkin A.V.2, Kepman A.V.2, Fedorov A.Y.1
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Afiliações:
- Lobachevsky Nizhny Novgorod State University
- Lomonosov Moscow State University
- Edição: Volume 61, Nº 1 (2025)
- Páginas: 45-54
- Seção: ЭКСПЕРИМЕНТАЛЬНЫЕ СТАТЬИ
- URL: https://aspvestnik.ru/0514-7492/article/view/682053
- DOI: https://doi.org/10.31857/S0514749225010025
- EDN: https://elibrary.ru/AGETEI
- ID: 682053
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Resumo
The method of obtaining bismaleimide monomers from aromatic diamines is optimized; the synthesis was tested on gram quantities with the possibility of further adaptation to kilogram quantities. Also, in order to obtain copolymers of bismaleimides with bisphenols, the conditions for obtaining diallyl bisphenol A were optimized.
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Sobre autores
E. Kudryashova
Lobachevsky Nizhny Novgorod State University
Email: afedorovNN@yandex.ru
Rússia, 23, Gagarin Ave., Nizhny Novgorod, 603950
V. Otvagin
Lobachevsky Nizhny Novgorod State University
Email: afedorovNN@yandex.ru
Rússia, 23, Gagarin Ave., Nizhny Novgorod, 603950
K. Romanov
Lobachevsky Nizhny Novgorod State University
Email: afedorovNN@yandex.ru
Rússia, 23, Gagarin Ave., Nizhny Novgorod, 603950
E. Afanasyeva
Lomonosov Moscow State University
Email: afedorovNN@yandex.ru
Rússia, 1, Leninskie Gory, Moscow, 119991
O. Morozov
Lomonosov Moscow State University
Email: afedorovNN@yandex.ru
Rússia, 1, Leninskie Gory, Moscow, 119991
A. Babkin
Lomonosov Moscow State University
Email: afedorovNN@yandex.ru
Rússia, 1, Leninskie Gory, Moscow, 119991
A. Kepman
Lomonosov Moscow State University
Email: afedorovNN@yandex.ru
Rússia, 1, Leninskie Gory, Moscow, 119991
A. Fedorov
Lobachevsky Nizhny Novgorod State University
Autor responsável pela correspondência
Email: afedorovNN@yandex.ru
Rússia, 23, Gagarin Ave., Nizhny Novgorod, 603950
Bibliografia
- D’Alelio G., Пат US3929713A (1975). США.
- Kablov E.N., Erofeev V.T., Rimshin V.I., Zotkina M.M., Dergunova A.V., Moiseev V.V. J. Phys.: Conf. Ser, 2020. 1687, 12031. doi: 10.1088/1742-6596/1687/1/012031
- Evsyukov S., Pohlmann T., ter Wiel M. Rev. Curr. Trends Polym. Sci. 2020. 20.
- Валуева М.И., Зеленина И.В., Жаринов М.А., Ахмадиева К.Р., Труды ВИАМ, 2019, 12, 67–79. D oi 10.18577/2307-6046-2019-0- 12-67-79
- Stenzenberger H. Struct. Adhes. Dev. resins Prim. Elsevier Applied Science Publishers, London; New York, 1986.
- Iredale R.J., Ward C., Hamerton I. Prog. Polym. Sci. Elsevier, 2017, 69. 1–21. doi: 10.1016/j.progpolymsci.2016.12.002
- Мухаметов Р.Р., Петрова А.П. Авиационные материалы и технологии. 2019, 3, 48–58. doi: 10.18577/2071-9140-2019-0-3-48-58
- Mangalgiri P.D. Def. Sci. J. Defence Scientific Information & Documentation Centre, 2005, 55, 175. doi: 10.14429/DSJ.55.1980
- Zahir A.-C., Renner A. Пат. US4100140A (1978). США.
- Crivello J. V. J. Polym. Sci. Polym. Chem. Ed., 1973, 11, 1185–1200. doi: 10.1002/pol.1973.170110607
- Bargain M., Combet A., Grosjean P. Пат. FR1555565 (1969). Франция.
- Михайлин Ю.А. Термоустойчивые полимеры и полимерные материалы. СПб.: Профессия, 2006.
- Tung C.M., Lung C.L., Liar T.T., Polym. Mat. Sci. Eng., 1985, 52, 139–143.
- Zahir S.A.-C., Renner A. Пат. US 4100140 (1978), США.
- Stenzenberger H.D. Bismaleimide Resins, ASM handbook, 2001.
- Бабкин А.В., Эрдни-Горяев Э.М., Солопченко А.В., Кепман А.В., Известия высших учебных заведений. Химия и химическая технология, 2015, 58, 54–57.
- Xiong X., Chen P., Zhang J., Yu Q., Wang B., Thermochim. Acta., 2011, 514, 44–50. doi: 10.1016/j.tca.2010.12.001
- Orphanides G.G. Пат. US4154737A (1979), США.
- Petride H., Beiu S., Florea C., Rosu I., Dragus C., Mihis I., Пат. RO116193B1 (1994), Румыния.
- Li K., Yuan Ch., Zheng S., Fang Q., Tetrahedron Lett., 2012, 53, 4245–4247. doi: 10.1016/j.tetlet.2012.06.025
- Groth T., Piejko K.-E., Joentgen W., Kasbauer J., Alig B., Striiver W. Пат. US5773630 A (1998), США.
- Liao D.C., Hsieh K.H. Journal of Polymer Science Part A: Polymer Chemistry, 1994, 32, 1665–1672. doi: 10.1002/pola.1994.080320908
- Hsieh K., Han J.L., Yu C.T., Fu S.C., Polymer, 2001, 42, 2491–2500. doi: 10.1016/S0032-3861(00)00641-8
- Armarego W.L.F., Chai C.L.L. Purification of organic chemicals, Butterworth‐Heinemann Oxford, 2012.
- Шошева А.Л., Труды ВИАМ, 2022, 10, 23–41. doi: 10.18577/2307-6046-2022-0-10-23-41
- Wang W., Gu J., Hua W., Jia X., Xi K., Chem. Commun., 2014, 50, 8889–8891. doi: 10.1039/C4CC03306J
- Choi H.Y., Chi D.Y. J. Am. Chem. Soc., 2001, 123, 9202–9203. doi: 10.1021/ja0164374
- Donovan B.R., Ballenas J.E., Patton D.L. Macromolecules, 2016, 49, 7667–7675. doi: 10.1021/acs.macromol.6b01822
- Maji S., Asrey R., Kumar S., Saxena C., Kumar N., Vyas K.D., Banerjee S., J. Appl. Polym. Sci., 2010. 116, 3708–3717. doi: 10.1002/app.31942
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