Acid–base sites synergistic catalysis over Mg–Zr–Al mixed metal oxide toward synthesis of diethyl carbonate. Issue 9 (26th January 2018)

• Record Type: Journal Article
• Authors: Yan, Tingting; Bing, Weihan; Xu, Ming; Li, Yinwen; Yang, Yusen; Cui, Guoqing; Yang, Lan; Wei, Min
• Is Part Of: RSC advances. Volume 8:Issue 9(2018)
• Page Start: 4695
• Page End: 4702
• Publication Date: 2018-01-26
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/c7ra13629c
• Languages: English
• ISSNs: 2046-2069

Abstract

Abstract : Mg/Zr/Al mixed metal oxides were prepared via a facile phase transformation process of hydrotalcite precursors, which showed acid–base sites synergistic catalytic performance toward the synthesis of diethyl carbonate from ethanol and urea. Abstract : In heterogeneous catalysis processes, development of high-performance acid–base sites synergistic catalysis has drawn increasing attention. In this work, we prepared Mg/Zr/Al mixed metal oxides (denoted as Mg2 Zr x Al1− x –MMO) derived from Mg–Zr–Al layered double hydroxides (LDHs) precursors. Their catalytic performance toward the synthesis of diethyl carbonate (DEC) from urea and ethanol was studied in detail, and the highest catalytic activity was obtained over the Mg2 Zr0.53 Al0.47 MMO catalyst (DEC yield: 37.6%). By establishing correlation between the catalytic performance and Lewis acid–base sites measured by NH3 -TPD and CO2 -TPD, it is found that both weak acid site and medium strength base site contribute to the overall yield of DEC, which demonstrates an acid–base synergistic catalysis in this reaction. In addition, in situ Fourier transform infrared spectroscopy ( in situ FTIR) measurements reveal that the Lewis base site activates ethanol to give ethoxide species; while Lewis acid site facilitates the activated adsorption of urea and the intermediate ethyl carbamate (EC). Therefore, this work provides an effective method for the preparation of tunable acid–base catalysts based on LDHs precursor approach, which can be potentially used in cooperative acid–base catalysis reaction.