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The role of metal–support interaction in catalytic activity of nanodiamond-supported nickel in selective phenylacetylene hydrogenationстатья
Статья опубликована в высокорейтинговом журнале
Информация о цитировании статьи получена из
Web of Science,
Scopus
Статья опубликована в журнале из списка Web of Science и/или Scopus
Дата последнего поиска статьи во внешних источниках: 8 февраля 2017 г.
- Авторы: Golubina E.V., Lokteva E.S., Erokhin A.V., Veligzhanin A.A., Zubavichus Ya V., Likholobov V.A., Lunin V.V.
- Журнал: Journal of Catalysis
- Том: 344
- Год издания: 2016
- Издательство: Academic Press
- Местоположение издательства: United States
- Первая страница: 90
- Последняя страница: 99
- DOI: 10.1016/j.jcat.2016.08.017
- Аннотация: Metal precursor coordination and its reduction mechanism in Ni catalysts supported on detonation nanodiamonds (ND) have been studied. TPR demonstrated multistage reduction of NiO supported on ND, which was explained by the presence of two types of Ni species on the ND surface. Weakly bonded Ni species are held on the ND surface by van der Waals forces, whereas strongly bonded ones are chemically bonded to the functional groups on the ND surface. Both Nisingle bondNi and Nisingle bondOsingle bondC scattering paths were found in Ni/ND catalysts using Morlet wavelet analysis of EXAFS data. The ratio of weakly and strongly bonded Ni species in the catalyst was tailored either by removal of functional groups by annealing of ND support in Ar at 900 °C or by calcination of NiO/ND precursor in air at 300 °C. The former resulted primarily in weakly bonded Ni species in the catalyst, while the latter led to strongly bonded ones. These two catalysts demonstrated drastic differences in selective styrene formation upon phenylacetylene hydrogenation: weakly bonded Ni species gave rise mainly to ethylbenzene, while Ni species strongly bonded to the surface through the Nisingle bondOsingle bondC bond afforded mainly styrene.
- Добавил в систему: Локтева Екатерина Сергеевна
Прикрепленные файлы
| № | Имя | Описание | Имя файла | Размер | Добавлен |
|---|---|---|---|---|---|
| 1. | Полный текст | 2016_JCat.pdf | 2,8 МБ | 18 ноября 2016 [Lokteva] |