Inhibition of terminal C-C bonds cleavage drives high selectivity of n-alkane hydroisomerization
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作者
Tan, Yangchun; Zhao, Yumeng; Li, Hanglin; Song, Xuechao; Chen, Bingbing; Du, Yanyan; Li, Jiusheng
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刊物名称
JOURNAL OF CATALYSIS
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年、卷、文献号
2023, 428, 1090-2694
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关键词
Tan, Yangchun; Zhao, Yumeng; Li, Hanglin; Song, Xuechao; Chen, Bingbing; Du, Yanyan; Li, Jiusheng
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摘要
Herein we develop a solvent-free one-pot synthesis strategy to simultaneously modify the size effect of metal sites and structural acidity on bifunctional catalysts to in-situ grow platinum nanoparticles (Pt-NPs - 1 nm and - 20 nm) of disparate sizes in the molecular sieve framework without relying on any ligand assistance, causing skeletal defects while exhibiting excellent catalytic performance in n-alkane hydroisomerization. It maintains almost 100 % isomerization selectivity at conversions below 90 %, with performance far superior to that of the conventional catalysts (Pt-NPs - 1 nm). The reason for high selectivity and high liquid yields was revealed by structural characterizations and density functional theory calculations, i.e., the inhibition of terminal C-C bond cleavage over n-dodecane chains adsorbed on the defect-containing catalysts and the higher energy barrier of transition state for producing gaseous small molecules, while the size of Pt-NPs may not be the main factor in determining the performance of n-alkane hydroisomerization.