克罗米亚
催化作用
乳酸
化学
路易斯酸
无机化学
铬
布朗斯特德-洛瑞酸碱理论
氧化钛
核化学
有机化学
细菌
生物
遗传学
作者
Atsushi Takagaki,Hiroshi Gotô,Ryuji Kikuchi,S. Ted Oyama
标识
DOI:10.1016/j.apcata.2018.11.018
摘要
A variety of silica-supported metal oxide catalysts were prepared by the incipient wetness impregnation method and were used for the conversion of dihydroxyacetone to lactic acid. A titanium oxide catalyst with Brønsted acid sites was selective to an intermediate, pyruvaldehyde and a chromium oxide catalyst with Lewis acid sites was selective to lactic acid. The co-impregnation of chromium- and titanium oxides with different ratios accelerated the reaction rate and improved the lactic acid yield up to 80% at 130 °C. Pyridine-adsorbed Fourier-transform infrared spectroscopy indicated that the silica-supported mixed oxides had both Brønsted acid and Lewis acid sites and the trend of the Lewis/Brønsted ratio was close to that of selectivity to lactic acid. Diffuse reflectance UV–vis spectroscopy showed that the silica-supported chromia-titania catalyst composed of isolated Cr and Ti species in tetrahedral coordination. Kinetic analysis revealed that the two critical rate constants, pyruvaldehyde formation and lactic acid formation, for the chromia-titania catalyst were much higher than those of the titania and chromia catalysts.
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