Role of internal coke for deactivation of ZSM-5 catalysts after low temperature removal of coke with NO2

被引:38
作者
Barbera, Katia [1 ,2 ]
Sorensen, Soren [3 ,4 ]
Bordiga, Silvia [1 ,2 ]
Skibsted, Jorgen [3 ,4 ]
Fordsmand, Henrik [5 ]
Beato, Pablo [5 ]
Janssens, Ton V. W. [5 ]
机构
[1] Univ Turin, Dept Inorgan Phys & Mat Chem, INSTM Ctr Riferimento, I-10125 Turin, Italy
[2] Univ Turin, NIS Ctr Excellence, I-10125 Turin, Italy
[3] Aarhus Univ, Dept Chem, Instrument Ctr Solid State NMR Spect, DK-8000 Aarhus C, Denmark
[4] Aarhus Univ, Interdisciplinary Nanosci Ctr iNANO, DK-8000 Aarhus C, Denmark
[5] Haldor Topsoe Res Labs, DK-2800 Lyngby, Denmark
关键词
METHANOL-TO-HYDROCARBONS; ZEOLITE H-BETA; ANGLE-SPINNING NMR; SOLID-STATE NMR; REACTION-MECHANISM; MAS NMR; REACTIVATION KINETICS; PERCOLATION APPROACH; LIGHT OLEFINS; MTO REACTION;
D O I
10.1039/c2cy00529h
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
By treating a deactivated ZSM-5 catalyst for the conversion of methanol to hydrocarbons with NO2, coke deposits can be removed at around 350 degrees C, which potentially enables catalyst regeneration at 350-400 degrees C, which is about 200 degrees C lower compared to a conventional regeneration in oxygen. To evaluate the regeneration with NO2 at 350 degrees C, the activity of a used ZSM-5 catalyst was measured after treatment with 1% NO2/He and 0.7% NO2/7% O-2/He at 350 degrees C, and 2% O-2/He at 550 degrees C. After the treatments with NO2 at 350 degrees C, some activity was restored, but the catalysts showed a fast deactivation. Temperature programmed desorption of ammonia and Al-27 MAS NMR measurements indicate that the amount of framework aluminium in the regenerated catalysts is about 60% of that in the fresh catalysts, and some redistribution of the aluminium takes place. Gravimetric temperature programmed oxidation showed that the catalysts still contain 0.3-0.6 wt% coke. GC-MS analysis of the retained species and very highspeed H-1 MAS NMR revealed that the remaining coke species are methyl benzenes, which are located inside the micropores of the ZSM-5 zeolite. It is concluded that the deactivation not only depends on the amount of coke, but also on the location of the coke in the catalyst.
引用
收藏
页码:1196 / 1206
页数:11
相关论文
共 69 条
[1]   Coke combustion and reactivation kinetics of a ZSM-5 zeolite based catalyst used for the transformation of methanol into hydrocarbons [J].
Aguayo, AT ;
Gayubo, AG ;
Olazar, M ;
Ortega, JM ;
Moran, AL ;
Bilbao, J .
CHEMICAL ENGINEERING COMMUNICATIONS, 1999, 176 :43-63
[2]   Z filtering in MQMAS NMR [J].
Amoureux, JP ;
Fernandez, C ;
Steuernagel, S .
JOURNAL OF MAGNETIC RESONANCE SERIES A, 1996, 123 (01) :116-118
[3]   Methanol-to-hydrocarbons reaction over SAPO-34. Molecules confined in the catalyst cavities at short time on stream [J].
Arstad, B ;
Kolboe, S .
CATALYSIS LETTERS, 2001, 71 (3-4) :209-212
[4]   Structure-deactivation relationship for ZSM-5 catalysts governed by framework defects [J].
Barbera, Katia ;
Bonino, Francesca ;
Bordiga, Silvia ;
Janssens, Ton V. W. ;
Beato, Pablo .
JOURNAL OF CATALYSIS, 2011, 280 (02) :196-205
[5]   COKE DEPOSITS ON H-ZSM-5 ZEOLITE [J].
BEHRSING, T ;
JAEGER, H ;
SANDERS, JV .
APPLIED CATALYSIS, 1989, 54 (03) :289-302
[6]   A PERCOLATION APPROACH FOR THE MODELING OF DEACTIVATION OF ZEOLITE CATALYSTS BY COKE FORMATION [J].
BEYNE, AOE ;
FROMENT, GF .
CHEMICAL ENGINEERING SCIENCE, 1990, 45 (08) :2089-2096
[7]   A PERCOLATION APPROACH FOR THE MODELING OF DEACTIVATION OF ZEOLITE CATALYSTS BY COKE FORMATION - DIFFUSIONAL LIMITATIONS AND FINITE RATE OF COKE GROWTH [J].
BEYNE, AOE ;
FROMENT, GF .
CHEMICAL ENGINEERING SCIENCE, 1993, 48 (03) :503-511
[8]   Conversion of methanol to hydrocarbons: the reactions of the heptamethylbenzenium cation over zeolite H-beta [J].
Bjorgen, M ;
Olsbye, U ;
Svelle, S ;
Kolboe, S .
CATALYSIS LETTERS, 2004, 93 (1-2) :37-40
[9]   The methanol-to-hydrocarbons reaction:: insight into the reaction mechanism from [12C]benzene and [13C]methanol coreactions over zeolite H-beta [J].
Bjorgen, M ;
Olsbye, U ;
Petersen, D ;
Kolboe, S .
JOURNAL OF CATALYSIS, 2004, 221 (01) :1-10
[10]   Conversion of methanol to hydrocarbons over zeolite H-ZSM-5: On the origin of the olefinic species [J].
Bjorgen, Morten ;
Svelle, Stian ;
Joensen, Finn ;
Nerlov, Jesper ;
Kolboe, Stein ;
Bonino, Francesca ;
Palumbo, Luisa ;
Bordiga, Silvia ;
Olsbye, Unni .
JOURNAL OF CATALYSIS, 2007, 249 (02) :195-207