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Bifunctional conversion of n-decane over HPW heteropoly acid incorporated into SBA-15 during synthesis
被引:160
作者:
Gagea, B. C.
[1
]
Lorgouilloux, Y.
[1
]
Altintas, Y.
[1
]
Jacobs, P. A.
[1
]
Martens, J. A.
[1
]
机构:
[1] Katholieke Univ Leuven, Ctr Surface Chem & Catalysis, B-3001 Heverlee, Belgium
关键词:
n-Decane hydroisomerization;
Heteropoly acids;
SBA-15;
synthesis;
Tungsten phosphoric acid;
Bifunctional catalysis;
SOLID ACID;
MESOPOROUS SILICA;
12-TUNGSTOPHOSPHORIC ACID;
SKELETAL ISOMERIZATION;
CATALYTIC-ACTIVITY;
THERMAL-STABILITY;
SULFATED ZIRCONIA;
H3PW12O40;
IMMOBILIZATION;
HYDROISOMERIZATION;
D O I:
10.1016/j.jcat.2009.04.017
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:
SBA-15 ordered mesoporous silica materials containing up to 40 wt.% of HPW heteropoly acid were synthesized via an original method involving the introduction of HPW in an acidified solution of P123 triblock copolymer (EO20PO70O20), the SBA-15 mesostructuring agent (direct synthesis). Samples with similar HPW loadings were also prepared by impregnation of SBA-15. Characterization by XRD, P-31 MAS NMR, NH3-TPD, and N-2 adsorption showed that even after calcination HPW in the direct synthesis samples was better dispersed than that in the impregnated samples. SBA-15-supported HPW materials were converted into bifunctional catalysts. In the conversion of n-decane, direct synthesis samples were superior to impregnated samples. The criteria of ideal bifunctional catalysis were fulfilled, e.g. high yields of skeletal isomers (>70%), of multi-branched skeletal isomers, and of branched cracked products, and hydrocracking reactions limited to primary cracking. Compared to ultrastable Y zeolites, the HPW/SBA-15 samples showed a broader optimum reaction temperature window for isomerization and higher n-decane dibranching selectivity. (C) 2009 Elsevier Inc. All rights reserved.
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页码:99 / 108
页数:10
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