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Selective hydrogenation of detrimental 4-nitrophenol to desired 4-aminophenol over potent PtCo intermetallic nanoparticles entrapped within the pores of Cr-BDC MOFs.

Authors :
Zahid, Muhammad
Jassim, Ghufran Sh.
Jawad, Hassan Ali M.
Khan, Muhammad Farooq
Ismail, Ahmed
Source :
Inorganic Chemistry Communications. Apr2023, Vol. 150, pN.PAG-N.PAG. 1p.
Publication Year :
2023

Abstract

[Display omitted] • PtCo IMNs were uniformly encaged within the mesopores of Cr-BDC MOFs for selective hydrogenation of 4-nitrophenole. • The PtCo/Cr-BDC catalyst exhibit superior selective hydrogenation performances than that of Pt/Cr-BDC and Co/Cr-BDC catalysts. • The exceptional activity was ascribed to mesoporous structure and synergistic interaction between Co and Pt in PtCo/Cr-BDC catalyst. • The mesoporous PtCo/Cr-BDC catalyst revealed remarkable durability. Engineering of economical and stabilized precious metal based catalysts are crucial in recent ages to achieve the desirable catalytic performance as they tend to destabilize easily. Herein, Cr-BDC MOF was prepared that provides high surface area and pore volumes to evenly distribute, host, and stabilize the Pt and Co intermetallic nanoparticles (IMNs). Among these, the PtCo/Cr-BDC catalyst showed superior selective hydrogenation activity for 4-Nitrophenol (4-NP) to 4-Aminophenol (4-AP) as an exemplary reaction. A number of characterization techniques were carried out to study the influence of the Cr-BDC support and Co metal on the surface and bulk structural properties of active Pt metal species. The Cr-BDC support imparts uniform distributions while the Co metal species influenced the catalytic activity. The maximum conversion (99.3 %) of 4-NP to 4-AP was observed with PtCo/Cr-BDC in 2 min at a reaction rate constant (k) of 1.27 min−1 at room temperature, which is superior than Pt/Cr-BDC (0.64 min−1) and Co/Cr-BDC (0.14 min−1). The superior hydrogenation activity was credited to the addition of electropositive Co species to Pt/Cr-BDC catalyst that synergistically interacts with active Pt species within the pores of Cr-BDC MOFs and making PtCo IMNs system. As a result of this synergistic interaction, new additional interfacial electrophilic and nucleophilic metallic sites are generated within the pores of MOFs, which enormously encourage the selective hydrogenation of lethal 4-NP to valued 4-AP. Besides, the PtCo/Cr-BDC catalysts revealed remarkable durability up to several repeated rounds, validating its real-world applicability. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
13877003
Volume :
150
Database :
Academic Search Index
Journal :
Inorganic Chemistry Communications
Publication Type :
Academic Journal
Accession number :
162362115
Full Text :
https://doi.org/10.1016/j.inoche.2023.110549