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Structured MFI film catalysts and adsorbents

Öhrman, Olov (author)
Luleå : Luleå tekniska universitet, 2005
English 51 s.
Series: Doctoral thesis / Luleå University of Technology 1 jan 1997 → …, 1402-1544 ; 2005:07
  • Doctoral thesis (other academic/artistic)
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  • A method originally developed at the division of Chemical Technology, Luleå University of Technology was tailored for the preparation of well-defined ZSM-5 films and zoned MFI films on supports suitable for catalysis and adsorption applications. Films were grown on monoliths, ceramic foams, alumina beads, soda glass beads and quartz glass. The supports were seeded with silicalite-1 crystals and hydrothermally treated in a single or several steps. The materials were evaluated by scanning electron microscopy, x-ray diffraction, N2 and NO2 sorption, x-ray photoelectron spectroscopy, ICP-AES, p-xylene isomerization and cracking of 1,3,5-tri-isopropylbenzene. The thickness of the continuous films could be controlled from 110 nm to 9 µm. Zoned MFI films were prepared from precursor ZSM-5 films by overgrowth with silicalite-1. A multi-step synthesis protocol was used to prevent excessive bulk crystallization. Ultrasound treatment was beneficial for removal of loosely attached crystals on top of the zeolite films. Defects such as cracks and open grain boundaries were observed by SEM and in concert, mesopores were observed by N2 sorption. Model parameters were fitted to experimental data from catalytic test reactions and these parameters indicated that thicker films contained more defects, probably in the form of open grain boundaries and cracks (mesopores) as observed by SEM and N2 sorption. Films supported on quartz were more catalytically active than films on alumina and soda glass. This was attributed to partial poisoning of the acid sites in the films on the latter two substrates, probably due to solid-state ion exchange of impurities such as alkali metals from the alumina and soda glass support to the film. As expected, thicker films possessed higher diffusion resistance than thin films. Surprisingly, a higher external activity was observed after zoning. This was attributed to formation of mesopores, migration of aluminum from the precursor ZSM-5 film to the external surface, and increased surface roughness upon zoning. ZSM-5 films supported on monoliths were successfully tested for NO2 sorption. As expected, the adsorption capacity per g zeolite was independent of film thickness. Formation of NO was observed as a result of NO2 adsorption on strong sites. Thicker films resulted in higher diffusion resistance as expected. The present work has resulted in substantial and valuable new fundamental understanding of the performance of thin molecular sieve film catalysts and adsorbents. These findings may facilitate development of novel materials for industrial applications.

Subject headings

TEKNIK OCH TEKNOLOGIER  -- Kemiteknik -- Kemiska processer (hsv//swe)
ENGINEERING AND TECHNOLOGY  -- Chemical Engineering -- Chemical Process Engineering (hsv//eng)

Keyword

Chemical Technology
Kemisk teknologi

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dok (subject category)

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Öhrman, Olov
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ENGINEERING AND TECHNOLOGY
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Luleå University of Technology

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