Catalytic Transfer Hydrogenation as a Hydrodesulfurization Method Using Isopropanol as a Hydrogen Donor | Sciact - CRIS-система Института катализа

Catalytic Transfer Hydrogenation as a Hydrodesulfurization Method Using Isopropanol as a Hydrogen Donor Научная публикация

Журнал

Fuel
ISSN: 0016-2361 , E-ISSN: 1873-7153

Вых. Данные

Год: 2026, Том: 406, Part B, Номер статьи : 136968, Страниц : 12 DOI: 10.1016/j.fuel.2025.136968

Авторы

Nesterov Nikolai ¹ , Philippov Alexey ¹ , Predein Alexander ¹ , Romanov Alexander ¹ , Pakharukova Vera ¹ , Prosvirin Igor ¹ , Salomatina Anna ¹ , Klimov Oleg ¹ , Martyanov Oleg ¹

Организации

1	Boreskov Institute of Catalysis SB RAS, Academician Lavrentiev ave. 5, Novosibirsk 630090, Russia

Информация о финансировании (1)

Российский научный фонд

24-13-00208

This study investigates novel catalytic transfer hydrogenation (CTH) strategies for the reductive removal of nitrogen (N)-, oxygen (O)-, and sulfur (S)-containing functional groups from model compounds representing heteroatomic constituents of heavy oil fractions. Isopropanol serves as the hydrogen donor, while heterogeneous catalysts based on molybdenum (Mo)-, nickel-molybdenum (Ni-Mo)-, and cobalt-molybdenum (Co-Mo)-containing sulfide systems, supported on aluminum oxide, are employed. Experiments were conducted in an autoclave reactor at temperatures ranging from 250 to 300 °C and pressures between 7.5 and 12.0 MPa. The results indicate that under these conditions, the N-containing indole does not undergo denitrogenation; instead, alkylation of the indole is the predominant reaction. Benzofuran, an O-containing model compound, undergoes reductive transformations characterized by the sequential hydrogenation of the aromatic ring containing the oxygen atom, followed by C-O bond cleavage. The most efficient heteroatom removal is observed for S-containing compounds such as benzothiophene and dibenzothiophene. For benzothiophene, a sequential desulfurization mechanism is evident, involving initial dearomatization of the sulfur-containing ring. In contrast, dibenzothiophene undergoes direct sulfur removal without the formation of intermediate hydrogenation products.

Nesterov N. , Philippov A. , Predein A. , Romanov A. , Pakharukova V. , Prosvirin I. , Salomatina A. , Klimov O. , Martyanov O.
Catalytic Transfer Hydrogenation as a Hydrodesulfurization Method Using Isopropanol as a Hydrogen Donor
Fuel. 2026. V.406, Part B. 136968 :1-12. DOI: 10.1016/j.fuel.2025.136968 WOS Scopus OpenAlex

Поступила в редакцию:	15 июл. 2025 г.
Принята к публикации:	25 сент. 2025 г.
Опубликована online:	30 сент. 2025 г.
Опубликована в печати:	15 февр. 2026 г.

Web of science:	WOS:001589849600012
Scopus:	2-s2.0-105017234079
OpenAlex:	W4414642627

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