Efficient esterification over hierarchical Zr-Beta zeolite synthesized via liquid-state ion-exchange strategy

Abstract

The eco-friendly zeolite-based solid acid catalysts constitute an important alternative to the liquid acid catalyst for the production of plasticizer tributyl citrate (TBC), due to their non-corrosive, high hydrothermal stability and easiness to recycle. Herein, a simple acid treatment to the H-Beta zeolite and subsequent incorporation of ZrIV ions into the vacated Al sites were conducted by liquid-state ion-exchange of ZrO(NO3)2 aqueous solution. The ZrIV ions were incorporated into the framework by the expand of the unit cell size, verified by XRD patterns, the emerging new band at ∼198 nm on UV–vis spectra, the enhanced binding energies of the Zr 3d5/2 and Zr 3d3/2 on XPS spectra, as well as the variations of isolated terminal silanol groups (Si-OH) by FTIR and the change of integrated intensity ratio of Q3/Q4 by 29Si MAS NMR. It was illustrated that the Lewis acid sites was the main active sites for esterification reaction and the produced abundant mesopores in the Zr-Beta-x catalysts would facilitate the transportation of TBC. The maximum conversion of citric acid as high as 80 % was obtained on Zr-Beta-128 (SiO2/ZrO2 molar ratio = 128) catalyst with the highest Lewis acid amount. Furthermore, the Zr-Beta-128 zeolite exhibited high stability without any detectable deactivation after 6 cycles with the 100 % selectivity to TBC. The efficient Zr-Beta catalyst could supply a novel possibility for the development of an environmentally-friendly solid acid catalyst with good performance for the TBC production.