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Ionic Liquids
and Methine Conversion
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| Molecular design of
new classes of ionic liquids and
modeling of ionic liquid properties
for novel applications are a significant
effort for PEER.
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1.
One of major effort in this
field at PEER is to develop
specific ionic liquids (IL)
for low temperature methane
conversion process. In an
environment with a powerful
catalyst such as Periana's
catalyst1 which can react
with methane readily a very
reaction inert ionic liquid
is needed as the reaction
media. We are working to
develop ionic liquids which
are chemical reaction-resistant,
acid- and thermo- stable2.
Also the ionic liquids should
enhance the methane conversion
selectively, such as conversion
to methanol.
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2.
Second interest in this field
is to design and synthesize
ionic liquids which have specific
catalytic functions. By study
and understanding of chemical
reaction mechanism in ionic
liquids we try to incorporate
or mobilize homogeneous transition-metal
complexes or Lewis acids to
specifically designed ionic
liquids for catalysis reactions
such as alkylation of aromatics.
These studies involve new
IL and transition metal complex
synthesis as well as monitoring
of reaction kinetics. New
compounds are prepared using
specialized vacuum line, Schlenk,
and glove box techniques,
and are usually characterized
by multinuclear NMR, UV-Vis,
and FT-IR, LC-MS, GC spectrometry
and by single crystal X-ray
diffraction methods.
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Other directions include developing
functionalized ionic liquids
for gas or liquid separation,
purification, new materials
and for heat transfer media.
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| Homogeneous Catalysis
in Ionic Liquids
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Homogeneous
catalysis usually takes
place in common organic
solvents. However, the majority
of solvents which are utilized
for homogeneous industrial
catalysis are volatile organic
compounds (VOCs) such as
halohydrocarbons, hydrocarbons
or ethers. It has been estimated
that global expenditures
on VOCs approach approximately
30 billion pounds which
means the unavoidable escape
of vapor from such a large
volume of solvents has a
tremendous effect on our
earth environment. Reaction
in ionic liquids will reduce
significantly the release
of VOCs. Also charged IL
solvent properties will
play chemistry differently
than common organic solvents.
At PEER using IL as media
for homogeneous catalysis
is a main direction in this
field.
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| Catalysis for Low
Temperature Natural Gas to Hydrogen
Conversion
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Hydrogen-fueled fuel cells
promise clean, efficient,
and sustainable energy that
will help world meet its
energy needs in the coming
century and beyond. The
U.S. consumed 7.9 million
barrels of gasoline per
day in January 2003, and
worldwide production of
hydrogen is about 100 million
kilograms per day. Most
of hydrogen is produced
from natural gas by steam
methane reforming process
at very high temperature
(900° C). PEER is now
engaged in development of
low cost and low temperature
process for production of
hydrogen. Methane is a particularly
attractive substrate for
such conversions since it
is cheap and readily available.
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We try to develop unique
catalysts and specific reaction
media for the process. An
organometallic compound
Os(amine)43+(2)
,which was previously developed
by Li and Taube 2,
seems close this goal. When
2 is reduced to Os2+, it
is endorsed a tremendous
ability to quickly grab
two hydrogen at room temperature
from same carbon center
in a hydrocarbon molecular.
This could be developed
to a catalyst with a specially
designed Ionic Liquid reaction
media for the methane transformation
at low temperature (room
temperature or below 200°
C) :
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| Develop New Catalysts
for Other Important Organic Reactions.
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PEER also is in process
of development of many other
synthetically important
homogeneous organic catalysis
reactions such as Grubbs'
catalyst or Sharpless' catalyst
for reaction in ionic liquids.
Work involves the mobilization,
stabilization of the catalysts
and elucidations of the
catalysis mechanism.
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Project: Using
Ionic Liquids in Selective Hydrocarbon
Conversion Processes
Sponsor: U. S. Department
of Energy(DOE)
Co-sponsors: ChevronTexaco
and Sachem
Project Dates: Start: 07/01/2004;
End: 06/30/2008
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References
1. Roy.A. Periana, et al., Science,
1998, 280, 340
2. Zai-Wei Li and Henry Taube, J.
Am. Chem. Soc. 1994, 116,
p11584-11585.
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