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Nickel Catalysts on Carbon-Mineral Sapropel-Based Supports for Liquid-Phase Hydrogenation of Nitrobenzene Научная публикация

Журнал Catalysts
, E-ISSN: 2073-4344
Вых. Данные Год: 2023, Том: 13, Номер: 1, Номер статьи : 82, Страниц : 14 DOI: 10.3390/catal13010082
Ключевые слова sapropel; supported nickel catalyst; liquid-phase nitrobenzene hydrogenation
Авторы Terekhova Elena N. 1 , Belskaya Olga B. 1 , Izmaylov Rinat R. 1 , Trenikhin Mikhail V. 1 , Likholobov Vladimir A. 2
Организации
1 Center of New Chemical Technologies, Boreskov Institute of Catalysis, 54 Neftezavodskaya Street, 644040 Omsk, Russia
2 Boreskov Institute of Catalysis, Siberian Branch, Russian Academy of Sciences, 5 Acad. Lavrentieva Ave., 630090 Novosibirsk, Russia

Информация о финансировании (1)

1 Министерство науки и высшего образования Российской Федерации 0239-2021-0004

Реферат: Nickel catalysts with carbon-mineral supports derived from sapropel were synthesized; the effect exerted by the nature of the support (type of the initial sapropel) and active component precursor on the activity of the catalysts in the model reaction of liquid-phase nitrobenzene hydrogenation was studied. The catalysts, synthesized using the support with a smaller fraction of carbon, were more active irrespective of the precursor nature. The highest activity was observed for the catalysts synthesized from nickel nitrate and formate; nitrobenzene conversion was 65% and 51%, respectively, after 1 h of reaction. The catalysts retained high activity after six reaction cycles at 100% aniline selectivity. The presence of sulfur in the nickel precursor deteriorated the catalytic activity (convection less than 3%) due to formation of the sulfide phase.
Библиографическая ссылка: Terekhova E.N. , Belskaya O.B. , Izmaylov R.R. , Trenikhin M.V. , Likholobov V.A.
Nickel Catalysts on Carbon-Mineral Sapropel-Based Supports for Liquid-Phase Hydrogenation of Nitrobenzene
Catalysts. 2023. V.13. N1. 82 :1-14. DOI: 10.3390/catal13010082 WOS Scopus РИНЦ OpenAlex
Даты:
Поступила в редакцию: 2 дек. 2022 г.
Принята к публикации: 27 дек. 2022 г.
Опубликована online: 31 дек. 2022 г.
Опубликована в печати: 1 янв. 2023 г.
Идентификаторы БД:
Web of science: WOS:000917107200001
Scopus: 2-s2.0-85146630683
РИНЦ: 50506148
OpenAlex: W4313397864
Цитирование в БД:
БД Цитирований
OpenAlex 1
Scopus 1
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