Mechanistic studies of transformations over zeolite catalysts probed by novel solid state NMR methods /

Since their introduction as cracking catalysts in the

Bibliographic Details
Main Author: Goguen, Patrick William
Format: Thesis Book
Language:English
Published: [Place of publication not identified] : [publisher not identified] ; 1997.
Subjects:
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Description
Summary:Since their introduction as cracking catalysts in the
sixties, zeolites have played a critical role in the American
chemical industry. A primary consideration for the design of
improved processes utilizing zeolites is the elucidation of
the reaction mechanisms by which transformations occur over
these materials. In situ solid state NMR has proven to be a
most useful methodology for the study of zeolite chemistry
which is largely responsible for our current understanding of
zeolites as nonsuperacidic, shape selective, solid acid
catalysts. While in situ methods are mature technologies,
current state of the art in situ experimentation suffers from
an overdependence on sealed microreactors where the chemistry
is studied at long contact times. This does not well
represent the conditions of industrial flow reactors, where
short contact times and kinetic effects are commonplace.
While some flow NMR probes have been developed, their static
nature renders them unable to take advantage of magic angle
spinning, an important line narrowing technique. The purpose
of this research was to develop solid state NMR technologies
allowing the study of heterogeneous chemical transformations
under flowing conditions and at much shorter time scales then
previously reported. The first novel technology presented is
a solid state NMR probe which allows for the in situ
activation and loading of a zeolite sample under flowing
conditions while still allowing MAS. This probe was used to
study the adsorption / desorption behavior of organics on
HZSM-5. The second novel protocol is a pulse quench reactor:
a microreactor which prepares samples for study under flowing
conditions and makes provision for the rapid (hundreds of
milliseconds) cooling of the sample from reaction temperature
in order to probe short reaction time scales. Studies of the
transformation of methanol to gasoline showed this process
not to proceed consecutively from the initial olefins as
commonly proposed, but rather through a hydrocarbon pool
mechanism. Acetone condensation was also studied and shown
to be a bimolecular process. Cyclopentenyl cations are shown
to form in both systems, species which were never observed in
the many previous in situ studies carried out in batch mode.
Item Description:Vita.
"Major Subject: Chemistry".
Physical Description:xiv, 206 leaves : illustrations ; 28 cm.
Issued also on microfiche from University Microfilms Inc.
Bibliography:Includes bibliographical references: pages 160-169.