Development of Methods for the Synthesis of Bis-( N -Maleimide)aryl and Bis-Diallyl Bisphenol Monomers for Thermosetting Polymers

E. S. Kudryashova; Кудряшова Е. С.; V. F. Otvagin; Отвагин В. Ф.; K. A. Romanov; Романов К. А.; E. S. Afanasyeva; Афанасьева Е. С.; O. S. Morozov; Морозов О. С.; A. V. Babkin; Бабкин А. В.; A. V. Kepman; Кепман А. В.; A. Yu. Fedorov; Федоров А. Ю.

doi:10.31857/S0514749225010025

Development of Methods for the Synthesis of Bis-(N-Maleimide)aryl and Bis-Diallyl Bisphenol Monomers for Thermosetting Polymers

作者: 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
隶属关系:
1. Lobachevsky Nizhny Novgorod State University
2. Lomonosov Moscow State University
期: 卷 61, 编号 1 (2025)
页面: 45-54
栏目: 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

如何引用文章

全文:

开放存取

##reader.subscriptionAccessGranted##
受限制的访问

订阅存取

详细
全文:
作者简介
参考
补充文件
统计

详细

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.

关键词

bismaleimide binders, monomers, 4,4’-bismaleimidodiphenylmethane, 2,4-bismaleimidotoluene, diallyl bisphenol A thermosetting polymers

全文:

作者简介

E. Kudryashova

Lobachevsky Nizhny Novgorod State University

Email: afedorovNN@yandex.ru
俄罗斯联邦, 23, Gagarin Ave., Nizhny Novgorod, 603950

V. Otvagin

Lobachevsky Nizhny Novgorod State University

Email: afedorovNN@yandex.ru
俄罗斯联邦, 23, Gagarin Ave., Nizhny Novgorod, 603950

K. Romanov

Lobachevsky Nizhny Novgorod State University

Email: afedorovNN@yandex.ru
俄罗斯联邦, 23, Gagarin Ave., Nizhny Novgorod, 603950

E. Afanasyeva

Lomonosov Moscow State University

Email: afedorovNN@yandex.ru
俄罗斯联邦, 1, Leninskie Gory, Moscow, 119991

O. Morozov

Lomonosov Moscow State University

Email: afedorovNN@yandex.ru
俄罗斯联邦, 1, Leninskie Gory, Moscow, 119991

A. Babkin

Lomonosov Moscow State University

Email: afedorovNN@yandex.ru
俄罗斯联邦, 1, Leninskie Gory, Moscow, 119991

A. Kepman

Lomonosov Moscow State University

Email: afedorovNN@yandex.ru
俄罗斯联邦, 1, Leninskie Gory, Moscow, 119991

A. Fedorov

Lobachevsky Nizhny Novgorod State University

编辑信件的主要联系方式.
Email: afedorovNN@yandex.ru
俄罗斯联邦, 23, Gagarin Ave., Nizhny Novgorod, 603950

参考

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