Purified CaO supported Pt nanoparticles for the selective hydrogenation of styrene oxide with enhanced selectivity of 1-phenylethanol

被引:0
|
作者
Zhao, Chenqi [1 ,2 ]
You, Rixin [2 ]
Jin, Meihua [2 ]
Jin, Xing [2 ]
Wu, Pingfan [1 ]
He, Meng [2 ]
Liang, Minghui [2 ]
机构
[1] Hubei Univ Technol, Inst POM based Mat, Sch Mat & Chem Engn, New Mat & Green Mfg Talent Intro & Innovat Demonst, Wuhan 430068, Hubei, Peoples R China
[2] Chinese Acad Sci, Natl Ctr Nanosci & Technol, Key Lab Nanosyst & Hierarch Fabricat, Ctr Excellence Nanosci, 11 Beiyitiao Zhongguancun, Beijing 100190, Peoples R China
关键词
ANTI-MARKOVNIKOV ALCOHOLS; EPOXIDE HYDROGENOLYSIS; CATALYST; RUTHENIUM; OXIDATION; PLATINUM;
D O I
10.1039/d4nj00957f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The CaO-supported Pt nanoparticle catalysts, herein referred to as the Pt/CaO-P catalysts, were synthesized for the first time to catalyze the selective hydrogenation of styrene oxide. All previously reported Pt- and Pd-based catalysts were prepared and evaluated under identical conditions, with 2-phenylethanol (2-PEA) being identified as the primary product in the selective hydrogenation of styrene oxide. The comparative analysis of the catalytic performance of Pt/CaO-P, Pt/CaO (unpurified), Pt/Ca(OH)2, and Pt/CaCO3 revealed that the purity of CaO is crucial for enhancing the selectivity towards 1-phenylethanol (1-PEA). Notably, the highest selectivity of 1-PEA over Pt/CaO-P reached up to 39%. Our SO-TPD, CO2-TPD and ex situ FT-IR results further indicated that strong basic sites can modify the adsorption site of SO over Pt nanoparticles, leading to the higher selectivity of 1-PEA. A proposed reaction mechanism for the ring opening of styrene oxide suggests that the breakage of conjugation between the benzene ring and the adjacent carbon cation by strong basic sites plays an important role. The purified CaO supported Pt nanoparticles exhibit the best selectivity toward 1-phenylethanol in the selective hydrogenation of styrene oxide.
引用
收藏
页码:10253 / 10261
页数:9
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