化学
钴
钼
无机化学
催化作用
锶
程序升温还原
钙钛矿(结构)
核化学
结晶学
有机化学
作者
Meloth Bhavisha,S. Aswani,A. Sreenavya,P. P. Neethu,I. Gopinathan Archana,S. Balamurugan,V. Ganesh,Ayyamperumal Sakthivel
标识
DOI:10.1002/ejic.202200590
摘要
Abstract SrBO 3−δ (B=Fe & Co) type perovskite oxides and their 25 % molybdenum doped counterparts, SrFe 0.75 Mo 0.25 O 3−δ (SFMO) and SrCo 0.75 Mo 0.25 O 3−δ (SFCO) are synthesized by the conventional solid‐state method and systematically characterized using Fourier transfer infrared spectroscopy, powder X‐ray diffraction, thermo‐gravimetric analysis, nitrogen sorption, and temperature‐programmed reduction. The powder X‐ray diffraction patterns and FTIR spectral analysis evident the formation of the pure cubic phase and the doping of molybdenum into the perovskite crystal lattice. The variable oxidation states of iron and cobalt and the formation of oxygen vacancies are apparent from the TPR‐H 2 and TGA curves, respectively. All of the samples have a lower surface area than porous materials, which is typical of the bulk oxide character. The iron‐based perovskite demonstrated superior activity to the cobalt‐based one for the oxidation of iso‐eugenol to 4‐hydroxy‐3‐methoxybenzaldehyde (vanillin) when employing aqueous H 2 O 2 as the oxidant. The maximum conversion of 73 % with 63 % selectivity for vanillin was obtained within 1.5 h at 60 °C over the SFMO catalyst. The catalytic conversion was almost similar upon re‐use of the catalyst.
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