Chlorobenzene hydrodechlorination on bimetallic catalysts prepared by laser electrodispersion of NiPd alloyстатья

Статья опубликована в высокорейтинговом журнале

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Статья опубликована в журнале из списка Web of Science и/или Scopus
Дата последнего поиска статьи во внешних источниках: 20 августа 2018 г.

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1. Полный текст Pure_and_Applied_Chemistry_2018.pdf 5,6 МБ 20 августа 2018 [Dayra2268]

[1] Chlorobenzene hydrodechlorination on bimetallic catalysts prepared by laser electrodispersion of nipd alloy / E. V. Golubina, T. N. Rostovshchikova, E. S. Lokteva et al. // Pure and Applied Chemistry. — 2018. — Vol. 90, no. 11. — P. 1685–1701. NiPd bimetallic systems were for the first time synthesized by laser electrodispersion (LED) of the Ni77Pd23 alloy target followed by the deposition of produced bimetallic particles on a TEM copper grid and alumina granules. Selective area energy-dispersive analysis confirms the bimetallic nature of NiPd particles deposited on a TEM copper grid. Their mean size is 1.0 nm according to TEM. XPS data demonstrate that under deposition on alumina granules (total metal content of 0.005  wt.%), nickel in bimetallic particles nearly completely oxidizes to Ni2+ species predominantly in the form of aluminate. At the same time major part of palladium (84 %) exists in Pd0 but oxidizes to Pd2+ (80 %) during 6 months storage in air. Both metals are deposited on the external surface of alumina granules and localized in the same areas. In situ reduction of both metals by H2 in the catalytic cell of XPS spectrometer is hindered. Nickel is not reduced even at 450 oC, confirming the formation of NiAlOx , whereas palladium is reduced at higher temperatures compared to a similar monometallic catalyst. Nevertheless, NiPd/Al2O3 catalyst is more efficient in gas-phase chlorobenzene hydrodechlorination at 150–350 oC than Ni/Al2O3 and even Pd/Al2O3 , and much more stable. The difference may be caused by the formation of new active sites due to the contact between Pd0 and NiAlOx-modified support, and the protective action of spinel reacting with HCl by-product. [ DOI ]

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