Please use this identifier to cite or link to this item: https://dspace.ctu.edu.vn/jspui/handle/123456789/61276
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dc.contributor.authorCo, Thanh Thien-
dc.contributor.authorNguyen, Nhut Minh-
dc.contributor.authorVo, Ly Dinh Khang-
dc.date.accessioned2021-08-13T01:19:53Z-
dc.date.available2021-08-13T01:19:53Z-
dc.date.issued2021-
dc.identifier.issn2525-2321-
dc.identifier.urihttps://dspace.ctu.edu.vn/jspui/handle/123456789/61276-
dc.description.abstractIn this work, metal nanoparticles were successfully synthesized through the reduction of metal salts using reducing agents such as: ethylene glycol (EG) and sodium borohydride (NaBH₄). These metal nanoparticles were impregnated into the supports M-X (M = Ni, Pd; X = Bent, C, Zeolite, and AI₂O₃) in high yield. The physio-chemical properties of these catalysts were characterized by various techniques such as UV-Vis spectroscopy, powder X-ray diffraction (PXRD), Transmission electron microscopy (TEM) and the specific surface area of M-X was evaluated by N₂ adsorption isotherm analysis at 77 K. All results corroborated the loading process. Literally, TEM images indicated that the palladium and nickel nanoparticles size are 6 and 13 nm. respectively. The efficiency of these catalysts was performed on the transfer hydrogenation of various carbonyl substrates in the presence of potassium hydroxide at atmosphere pressure. The results showed that both nickel and palladium supported X catalysts exhibited high activities over 99 % within 60 min in the presence of potassium hydroxide.vi_VN
dc.language.isovivi_VN
dc.relation.ispartofseriesVietnam Journay of Chemistry;No.59(2) .- P.192-197-
dc.subjectNickelvi_VN
dc.subjectPalladium nanoparticlesvi_VN
dc.subjectNanocatalystsvi_VN
dc.subjectHydrogenationvi_VN
dc.subjectSupported catalystsvi_VN
dc.titleHighly efficient transfer hydrogenation of carbonyl compounds over supported nickel and palladium nanoparticlesvi_VN
dc.typeArticlevi_VN
Appears in Collections:Vietnam Journal of Chemistry

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