School of Chemistry and Chemical Engineering, Guangxi Key Laboratory of Petrochemical Resource Processing and Process Intensification Technology, Guangxi University, 100 Daxue Road, Nanning, 530004, P. R. China.
Chemphyschem. 2023 May 16;24(10):e202200703. doi: 10.1002/cphc.202200703. Epub 2023 Mar 6.
Ni-Ti intercalated bentonite catalysts (Ni-Ti-bentonite) and Ni-TiO supported bentonite catalysts (Ni-TiO /bentonite) were prepared, and the effects of Ni-Ti supported and intercalated bentonite on the selective hydrogenation of cinnamaldehyde were investigated. Ni-Ti intercalated bentonite enhanced the Brønsted acid sites strength, decreased the acid amount and Lewis's acid sites strength, which inhibited the activation of the C=O bond and contributed to selective hydrogenation of the C=C bond. When Ni-TiO was supported on bentonite, the acid amount and Lewis's acid strength of the catalyst increased, providing additional adsorption sites and increased the acetals byproducts. Due to the higher surface area, mesoporous volume, and suitable acidity, compared with Ni-TiO /bentonite in methanol solvent, 2 MPa, 120 °C for 1 h, Ni-Ti-bentonite exhibited a higher cinnamaldehyde (CAL) conversion of 98.8 %, as well as a higher hydrocinnamaldehyde (HCAL) selectivity of 95 %, and no acetals were found in the product.
镍钛插层膨润土催化剂(Ni-Ti-bentonite)和负载镍钛的二氧化钛膨润土催化剂(Ni-TiO /bentonite)被制备出来,并研究了镍钛负载和插层膨润土对肉桂醛选择性加氢的影响。镍钛插层膨润土增强了 Brønsted 酸位强度,降低了酸量和Lewis 酸位强度,抑制了 C=O 键的活化,有利于 C=C 键的选择性加氢。当 Ni-TiO 负载在膨润土上时,催化剂的酸量和 Lewis 酸强度增加,提供了更多的吸附位,并增加了缩醛副产物。与甲醇溶剂中 Ni-TiO /bentonite 相比,Ni-Ti-bentonite 在 2 MPa、120°C 下反应 1 h 时,具有更高的肉桂醛(CAL)转化率 98.8%,更高的氢化肉桂醛(HCAL)选择性 95%,产物中没有发现缩醛。