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Cu modified VOx/Silicalite-1 catalysts for propane dehydrogenation in CO2 atmosphere
被引:8
|作者:
Chen, Yan
[1
]
Wang, Yuan
[1
]
Ma, Qingxiang
[1
]
Gao, Xinhua
[1
]
Zhao, Tian-Sheng
[1
]
机构:
[1] Ningxia Univ, Coll Chem & Chem Engn, State Key Lab High Efficiency Utilizat Coal & Gree, Yinchuan 750021, Peoples R China
来源:
关键词:
Cu modification;
Propane dehydrogenation;
High conversion;
CO2;
VOx/Silicalite-1;
OXIDATIVE DEHYDROGENATION;
CARBON-DIOXIDE;
ZEOLITE;
D O I:
10.1016/j.fuel.2023.130819
中图分类号:
TE [石油、天然气工业];
TK [能源与动力工程];
学科分类号:
0807 ;
0820 ;
摘要:
Propane dehydrogenation in CO2 atmosphere (PDH-CO2) is of interest with a potential to raise propane conversion. Here the catalytic performance of Cu modified 10VOx/Silicalite-1(S-1) for PDH-CO2 is presented for the first time. The initial propane conversion of 68.8% on 0.5Cu-10VOx/S-1 was reached from 59.3% on 10VOx/S-1, along with the CO2 conversion of 44.5% from 32.4%. The role of S-1 support and Cu modification were elucidated by means of X-ray diffraction (XRD), ultraviolet-visible diffuse reflection (UV-Vis), NH3/CO2 temperatureprogrammed desorption (NH3/CO2-TPD), H2 temperature-programmed reduction (H2-TPR) and X-ray photoelectron spectroscopy (XPS) characterization. While dispersing VOx, non-acidic S-1 minimized the side reactions usually occurring on the strong acidic sites. Cu modification promoted the dispersion of VOx and enabled 10VOx/ S-1 exposing more weak acidic sites and basic sites, boosting respectively the adsorption of propane and CO2, for concurrently accelerating the reverse water gas shift (RWGS). Moreover, the highly dispersed V5+ was formed on the surface whereas the percentage of inactive V3+ decreased.
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页数:8
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