TY - JOUR
T1 - In situ replacement of Cu-DEN
T2 - An approach for preparing a more noble metal nanocatalyst for catalytic use
AU - Onisuru, Oluwatayo Racheal
AU - Oseghale, Charles O.
AU - Meijboom, Reinout
N1 - Publisher Copyright:
© The Royal Society of Chemistry and the Centre National de la Recherche Scientifique.
PY - 2020/12/14
Y1 - 2020/12/14
N2 - The advantage of dendritic monodisperse macromolecules' dual templating ability was useful in the formation of silica-supported copper nanoparticles Cun@SiO2NPs. This was acquired by the initial synthesis of a silica framework (G4-PAMAM-NH2-SiO2) as a mesoporous support using amine-terminated generation 4 PAMAM dendrimers (G4-PAMAM-NH2). The encapsulated Cun@SiO2 NPs, calcined at 500 C, were made to undergo a displacement reaction with Au3+ generated from the equivalent molar addition of HAuCl4. This resulted in the formation of Aun@SiO2NPs upon in situ replacement at a regulated pH. The synthesized nanoparticles were characterized and examined. The catalysts were shown to be catalytically active in the hydrogenation of 4-nitrophenol, and oxidation of rhodamine B as model reactions, before oxidation of styrene using TBHP. Also, the stability of the catalyst was evaluated, and the catalytic activity was retained after three consecutive cycles.
AB - The advantage of dendritic monodisperse macromolecules' dual templating ability was useful in the formation of silica-supported copper nanoparticles Cun@SiO2NPs. This was acquired by the initial synthesis of a silica framework (G4-PAMAM-NH2-SiO2) as a mesoporous support using amine-terminated generation 4 PAMAM dendrimers (G4-PAMAM-NH2). The encapsulated Cun@SiO2 NPs, calcined at 500 C, were made to undergo a displacement reaction with Au3+ generated from the equivalent molar addition of HAuCl4. This resulted in the formation of Aun@SiO2NPs upon in situ replacement at a regulated pH. The synthesized nanoparticles were characterized and examined. The catalysts were shown to be catalytically active in the hydrogenation of 4-nitrophenol, and oxidation of rhodamine B as model reactions, before oxidation of styrene using TBHP. Also, the stability of the catalyst was evaluated, and the catalytic activity was retained after three consecutive cycles.
UR - http://www.scopus.com/inward/record.url?scp=85097756993&partnerID=8YFLogxK
U2 - 10.1039/d0nj04381h
DO - 10.1039/d0nj04381h
M3 - Article
AN - SCOPUS:85097756993
SN - 1144-0546
VL - 44
SP - 20322
EP - 20333
JO - New Journal of Chemistry
JF - New Journal of Chemistry
IS - 46
ER -