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Immobilized Pd complexes over MCM-41 as supported catalysts for effective reformation of hydrocarbons
被引:9
|作者:
Mishra, Gopal S.
[1
]
Kumar, Anil
[2
]
机构:
[1] Univ Tecn Lisboa, Inst Super Tecn, Ctr Quim Estrut, P-1049001 Lisbon, Portugal
[2] Indian Inst Technol, Dept Chem Engn, Kanpur 208016, Uttar Pradesh, India
关键词:
MODIFIED SILICA-GEL;
N-HEXANE;
ISOMERIZATION;
HYDROISOMERIZATION;
MECHANISM;
HEPTANE;
D O I:
10.1039/c1cy00170a
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
The ethylthio alkane ligands i.e. di(ethylthio) ethane, I, and di(ethylthio) propane, II, have been used for the synthesis of Pd(II) complexes. These complexes were covalently anchored to the modified MCM-41 matrix as supported hybrid catalysts (MCM-41/I as Pd-I and MCM-41/II as Pd-II). Remarkable catalytic effects were observed when these supported catalysts act in n-hexane and n-heptane reformation reactions in the presence of H-2. Catalyst Pd-I provided the high TONs of 2325 with 91% selectivity for n-hexane and high TONs of 2145 with 88% selectivity for n-heptane under optimized and relatively mild conditions. A carbenium-based mechanism has been included to explain the product formation. TGA analysis indicates that these catalysts were thermally stable up to the reaction temperature and recyclable for further utilization.
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页码:1224 / 1231
页数:8
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