In situ synthesized Pd nanoparticles supported on B-MCM-41: an efficient catalyst for hydrogenation of nitroaromatics in supercritical carbon dioxide

被引:42
作者
Chatterjee, Maya [1 ]
Ishizaka, Takayuki [1 ]
Suzuki, Toshishige [1 ]
Suzuki, Akira [1 ]
Kawanami, Hajime [1 ]
机构
[1] AIST, Res Ctr Compact Chem Syst, Miyagino Ku, Sendai, Miyagi 9838551, Japan
关键词
MESOPOROUS MOLECULAR-SIEVES; NITROBENZENE HYDROGENATION; SELECTIVE HYDROGENATION; BORON; MCM-41; LIQUID; CYCLOHEXANONE; STATE; NMR; LIMONENE;
D O I
10.1039/c2gc36160d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In situ synthesis of Pd nanoparticles supported on boron (B)-substituted MCM-41 (B-MCM-41) with Si/B ratio varying from 100 to 5 was carried out by hydrothermal method using H3BO3 as B source. The textural properties as well as thermal stability of the resultant material were investigated by XRD, TEM, FTIR and TG-DTA. Highly ordered materials were obtained depending on the Si/B ratio, which also influenced the particle size of Pd as well as dispersion. Pd/B-MCM-41 was a promising catalyst for the hydrogenation of nitrobenzene in supercritical carbon dioxide with exceptionally faster reaction rate [turnover frequency (TOF) = 5.2 x 10(5) h(-1) (144 s(-1))] and high yield of aniline (100%). The observed reaction rate was strongly influenced by the Pd particle size related to Si/B ratio and physical properties of CO2 such as pressure-and temperature-dependent solvent power. A comparison of catalytic activity with the Pd supported only on silica material of similar particle size inferred that the presence of even a small amount of B significantly changes the reaction rate from 70 (only Si) to 105 s(-1) (Si/B = 100). In addition, TOF of Pd/B-MCM-41 was high when compared with other Pd catalysts supported on Al-MCM-41 and Ga-MCM-41 obtained by a similar method, and follows the order: B (144 s(-1)) > Ga (31.2 s(-1)) > Al (10.2 s(-1)). The remarkable advantage of the present catalytic system involves low metal content (similar to 1%), easy separation and it is successfully employed for the hydrogenation of substituted nitroaromatics, nitrile and phenol under mild reaction conditions. Furthermore, the catalyst was recyclable up to the 7th recycle without any loss of catalytic activity.
引用
收藏
页码:3415 / 3422
页数:8
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