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Other
Areas of Research
Materials
Colloidal and Inertfacial Phenomena
Fluid Properties
Materials
In
keeping with the goal of the University of establishing centers
of excellence in specific research areas, another thrust of the
Department of Chemical Engineering is in materials. This research
includes both materials processing and materials characterization.
Fundamental processing studies include electrochemical reactions,
reactions in emulsions and microemulsions, sol-gel reactions, and
fractal interpretations. Both analytical modeling and laboratory
experimentation are involved.
Reactions in segregated media--micelles, microemulsions, vesicles,
etc.--aimed toward developing new applications are being studied.
Such media have several unique characteristics due to the dispersed
nature of the reactive regions. For example, not only is it possible
to handle extremely viscous, even solid materials while avoiding
heat transfer problems, but also localized control of the composition
of the reactive region can be achieved. These characteristics are
being evaluated as a means of producing bulk quantities of ultrafine
(<100nm) ceramics particles. By appropriate control of the process
variables, monodisperse suspensions can be produced which aid in
the production of low-defect final products. Of current interest
here is the production of precursor particles for the 1-2-3 superconductor.
In work related to magnetic data storage, we are electrodepositing
ultrathin layered alloy films and characterizing their morphology
and properties. Typical model systems consist of alternating layers
of ferromagnetic and nonmagnetic metal, for example, Ni/Cu/Ni trilayers
or Co/Cu/Co multilayers. When the thickness of the individual layers
is comparable to the mean free path of a conduction electron in
a metal i.e., several nanometers, the films have novel magnetic
properties that make them attractive candidates for new generation
data storage materials. The roughness of the interface between ferro-magnetic
and adjacent nonmagnetic regions can be controlled by choosing the
deposition conditions and appears to affect the film's magnetic
properties. Our work on electrodeposited ultrathin films is aimed
at elucidating the connections between the electro-deposition process
variables, the nanoscale film morphology, and the properties of
the films. We are using a combination of experiments and modeling
to study the processing, structure, and properties of these films.
Participating Faculty
KNona
Liddell, Professor
509 335-3710
Bill Thomson, Professor
509 335-8580
Richard Zollars,
Professor
509 335-4332
Recent Publications
R.F. Renner and K.C. Liddell, "Roughness Development
in Electrodeposited Ultrathin Cobalt and Nickel Layers." J. Mater.
Res., 15, 458 (2000).
Colloidal
and Interfacial Phenomena
Adsorption
into Hydrophobic Surfaces: The adsorption of nonionic surfactants
appears to be well behaved, with the surface area occupied per adsorbed
molecule increasing with increasing molecular weight of the surfactant,
and with increasing polarity of the adsorbing surface. The behavior
of anionic surfactants is quite different, however. Adsorption areas
appear to first increase, then decrease, with increasing molecular
weight for a series of sodium alkyl sulfates. Increasing the adsorbing
surface charge density initially decreases the adsorption area,
but ultimately results in a complete repulsion of the surfactant
from the surface. These differences in behavior appear to arise
from the interactions between the ionized groups chemically bound
to the adsorbing surface and those on the surfactant. This study
is examining the effect that these electrostatic interactions have
on the adsorption area per molecule for a series of anionic surfactants.
A newly developed theory for the adsorption of polymeric species
into hydrophobic surfaces has also been modified to include the
electrostatic forces necessary to model the adsorption of these
ionic surfactants.
Participating Faculty
Richard
Zollars, Professor
509 335-4332
Recent Publications
R. L. Zollars, "Ionic Absorbates on Hydrophobic
Surfaces", invited chapter in Surfaces of Nanoparticles and Porous
Surfaces, J. Schwarz and C. I. Contescu, Editors, Marcel Dekker,
Inc., New York, 1999.
P. Blau and R. L. Zollars, "Sedimentation Field Flow Fractionation
of Nonspherical Particles", Journal of Colloid and Interface
Science, 183, 476 (1996).
Fluid
Properties
A
magnetic-coupled microbalance system has been assembled to allow
extremely accurate measurements of densities of fluid mixtures,
including the region very near dew-point conditions. Investigations
are ongoing relative to development of improved equations of state,
with practical applications in the petroleum industry.
A microwave type measurement system has been constructed and is
being used to measure dielectric constants for aqueous solutions
containing dissolved solids and organic compounds. This property
is essential in modeling electrolyte solutions, with applications
in petroleum production, water purification, geochemistry, etc.
The microwave cell is also being used to investigate liquid-vapor
phase change phenomena in hydrocarbon mixtures.
Participating Faculty
Reid
Miller, Professor
509 335-4001
Recent Publications
G. S. Anderson, R. C. Miller and A. R. H. Goodwin,
"Static Dielectric Constants for Liquid Water from 300 K to 350
K at Pressures to 13 MPa Using a New Radio-Frequency Resonator",
J. Chem. Eng. Data, 45, 549 (2000).
E. F. May, R. C. Miller and Z. Shan, "Densities and Dew Points of
Vapor Mixtures of Methane + Propane and Methane + Propane + n-Hexane
Using a Dual-Sinker Densimeter", J. Chem. Eng. Data, (published
on web July 19) to ap-pear (2001).
E. F. May, T. J. Edwards, A. G. Mann, C. Edwards and R. C. Miller,
"Development of an Automated Phase Behavior Measurement System for
Lean Hydrocarbon Fluid Mixtures, using Re-Entrant RF/Microwave Resonant
Cavities", Fluid Phase Equilibria, 185, 339 (2001).
E. F. May, R. C. Miller and A. R. H. Goodwin, "Dielectric Constants
and Molar Polarizabilities for Vapor Mixtures of Methane + Propane
and Methane + Propane + Hexane Obtained with a Radio-Frequency Reentrant
Cavity", submitted to J. Chem. Eng. Data (2001).
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