4.6 Article

Mild Oxidation of Toluene to Benzaldehyde by Air

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INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
卷 62, 期 3, 页码 1688-1694

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AMER CHEMICAL SOC
DOI: 10.1021/acs.iecr.2c03967

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We report a green oxidation method for the conversion of toluene to benzaldehyde using air under mild conditions with over 99% selectivity at 35% conversion and 180 degrees C. Previous studies have made little progress in this important reaction, with low selectivity or conversion. In this work, a modified catalytic system using 1 MPa of air as an oxidant and optimized catalytic center is developed, which shows realistic feasibility for high-performance and atom economy benzaldehyde production.
We report here the green oxidation of toluene to benzaldehyde by air under mild conditions in >99% selectivity at 35% conversion at 180 degrees C. This is an important reaction in both theoretical and practical research studies, but little progress has been made in the past five decades. Either the selectivity or the conversion is very low, and the sum of selectivity and conversion is hardly more than one hundred. In previous investigation, we have constructed a highly efficient system of catalysis, i.e., Pickering-like emulsion of toluene in water stabilized by amphiphilic catalysts HDPA-FeOx/Al2O3, hexadecyl phosphonic acid-modulated iron oxides, which work in an enzyme-like mechanism for oxidation of toluene to benzaldehyde. However, the oxygen pressures more than 3 MPa needed for high conversion impede their practical uses. In this work, we modify the catalytic system for the green oxidation of toluene to benzaldehyde using 1 MPa of air as an oxidant. First, the catalytic center of HDPA-FeOx/Al2O3 is optimized as PPA-CuFeOx/Al2O3 with promoted activity of crystal oxygen toward toluene oxidation. Readily available phenylphosphonic acid (PPA), in place of HDPA, shows good performance in the new catalytic system. Second, 5 vol % acetone/water is used as a mixed solvent of the reaction, which markedly modifies the oxygen dissolving and transferring, the access of the toluene molecule to the catalyst, and the recovery rate of catalytic center. The acetone molecule itself, however, is proved not converted and can be recycled in the catalytic process. Comprehensively, the catalytic system including multifactor synergism and good intrinsic safety developed in the current work has realistic feasibility for benzaldehyde production from toluene green oxidation in high-performance and atomic economy.

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