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Scrap Tyre Rubber Depolymerization with Nitrous Oxide. Reaction Products and Mechanism Научная публикация

Журнал Iranian Polymer Journal
ISSN: 1026-1265 , E-ISSN: 1735-5265
Вых. Данные Год: 2014, Том: 23, Номер: 11, Страницы: 881-890 Страниц : 10 DOI: 10.1007/s13726-014-0284-1
Ключевые слова Nitrous oxide, Reclaimed rubber, Recycling, Scrap tyres
Авторы Dubkov Konstantin A. 1 , Semikolenov Sergey V. 1 , Ivanov Dmitriy P. 1 , Babushkin Dmitriy E. 1 , Voronchikhin Vasiliy D. 2
Организации
1 Boreskov Institute of Catalysis, Siberian Branch of the Russian Academy of Sciences, Pr. Akad. Lavrentieva 5, Novosibirsk 630090, Russia
2 Siberian State Technological University, Pr. Mira 82, Krasnoyarsk 660049, Russia

Информация о финансировании (2)

1 Российский фонд фундаментальных исследований 08-03-12071
2 Совет по грантам Президента Российской Федерации МК-5473.2013.3

Реферат: The development of effective methods for reclaiming scrap tyre rubbers attracts a great deal of attention. Earlier, we have proposed an alternative way for reclaiming waste rubber, which consists in its treatment with nitrous oxide (N2O) at 180–230 °C and pressure of 2–5 MPa. In the present study, the reclaimed products obtained by this method from tyre crumb rubber were characterized for the first time by TGA, FTIR, NMR, and ultimate analysis techniques. The results showed that the sol fraction isolated from the reclaimed rubber consists mainly of diene oligomers with the carbonyl, predominantly ketone, groups. The remaining gel fraction includes some of the rubber polymer components and all the carbon black filler present in the initial vulcanizate. Based on the experimental results, a mechanism of vulcanized rubber interaction with nitrous oxide was suggested. The mechanism involves a selective 1,3-dipolar cycloaddition of N2O molecules to C=C bonds of isoprene and butadiene units in vulcanized elastomers. The main reaction route proceeds without cleavage of initial C=C bonds leading to the formation of ketone groups randomly distributed along the polymer backbone. The cleavage of a certain amount of reacting C=C bonds leads to controllable scission of macromolecular chains and accordingly to depolymerization of the initial vulcanized rubber, thus yielding a plastic reclaim product. The sulfur cross-links do not appear to be broken in the course of waste rubber treatment.
Библиографическая ссылка: Dubkov K.A. , Semikolenov S.V. , Ivanov D.P. , Babushkin D.E. , Voronchikhin V.D.
Scrap Tyre Rubber Depolymerization with Nitrous Oxide. Reaction Products and Mechanism
Iranian Polymer Journal. 2014. V.23. N11. P.881-890. DOI: 10.1007/s13726-014-0284-1 WOS Scopus РИНЦ CAPlus OpenAlex
Даты:
Поступила в редакцию: 8 апр. 2014 г.
Принята к публикации: 23 сент. 2014 г.
Опубликована online: 10 окт. 2014 г.
Опубликована в печати: 1 нояб. 2014 г.
Идентификаторы БД:
Web of science: WOS:000344576900006
Scopus: 2-s2.0-84919907101
РИНЦ: 24022845
Chemical Abstracts: 2014:1743058
OpenAlex: W2022324835
Цитирование в БД:
БД Цитирований
Web of science 15
Scopus 18
РИНЦ 17
OpenAlex 20
Альметрики: