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Effect of Pd- Precursor and Support Acid Properties on the Pd Electronic State and the Hydrodesulfurization Activity of Pd-Zeolite Catalysts Научная публикация

Журнал Catalysis Today
ISSN: 0920-5861 , E-ISSN: 1873-4308
Вых. Данные Год: 2019, Том: 323, Страницы: 257-270 Страниц : 14 DOI: 10.1016/j.cattod.2018.07.058
Ключевые слова Deep hydrodesulfurization of diesel fractions; H-ZSM-5Pd-zeolite catalyst; Thiophene; Dibenzothiophene
Авторы Yashnik Svetlana A. 1 , Urzhuntsev Gleb A. 1 , Stadnichenko Andrei I. 1 , Svintsitskiy Dmitry A. 1 , Ishchenko Arcady V. 1 , Boronin Andrei I. 1 , Ismagilov Zinfer R. 1,2
Организации
1 Boreskov Institute of Catalysis SB RAS, Novosibirsk, 630090, Russia
2 Institute of Coal Chemistry and Materials Science, Kemerovo, Russia

Информация о финансировании (1)

1 Федеральное агентство научных организаций России 0303-2016-0014

Реферат: We studied on the function of Pd species located in mesopores and inside zeolite channels (micropores) of the montmorillonite-modified zeolite catalyst for the hydrodesulfurization of diesel fraction with 350 ppm of sulfur as DBT, 4-MDBT, and 4,6-DMDBT. It was shown that the ex-dihydrogentetrachloropalladate impregnated catalyst as well as the ex-tetraamminepalladium(II) chloride ion-exchanged catalyst have high efficiency of sulfur removal from the diesel fuel in temperature range 280–300 оC. The sulfur tolerance of catalyst depended on the method of Pd adding. The catalyst prepared by ion-exchange with tetraamminepalladium chloride solution exhibited the highest sulfur tolerance. According to FTIR of adsorbed CO, this catalyst contains a small Pd metal atoms or cluster in electron-deficient state inside zeolite channels. They probably ensure sulfur tolerance due to hydrogen spillover. The montmorillonite addivite significantly modifies performance of the Pd-Zeolite catalyst in hydrotreating of diesel fraction. It leads to a decrease of cracking function, while those of hydrogenolysis of sulfurorganic molecules and hydrogenation of aromatic molecules are strengthened in comparison with the unmodified catalyst. This effect is explained by the change of acidic properties of the catalyst, limitations of diffusion of various molecules into the zeolite channels, and diffusion of Pd from the zeolite channels.
Библиографическая ссылка: Yashnik S.A. , Urzhuntsev G.A. , Stadnichenko A.I. , Svintsitskiy D.A. , Ishchenko A.V. , Boronin A.I. , Ismagilov Z.R.
Effect of Pd- Precursor and Support Acid Properties on the Pd Electronic State and the Hydrodesulfurization Activity of Pd-Zeolite Catalysts
Catalysis Today. 2019. V.323. P.257-270. DOI: 10.1016/j.cattod.2018.07.058 WOS Scopus РИНЦ CAPlusCA OpenAlex
Даты:
Поступила в редакцию: 23 февр. 2018 г.
Принята к публикации: 31 июл. 2018 г.
Опубликована online: 2 авг. 2018 г.
Опубликована в печати: 15 февр. 2019 г.
Идентификаторы БД:
Web of science: WOS:000453555200028
Scopus: 2-s2.0-85051132075
РИНЦ: 35714868
Chemical Abstracts: 2018:1490887
Chemical Abstracts (print): 170:66522
OpenAlex: W2887781728
Цитирование в БД:
БД Цитирований
Scopus 23
РИНЦ 24
Web of science 22
OpenAlex 25
Альметрики: