

Education:
BS
(Chemistry): Furman
University, Greenville, SC;
1998; Research Advisor: John
F. Wheeler
Ph.D. (Chemistry): The University of Kansas,
Lawrence, KS; 2003; Dissertation Advisor: A. S. Borovik
Post-Doc: The
University of Michigan,
Ann Arbor, MI; 2003-2005; Advisor: Mark
E.
Meyerhoff
Fall 2007 Courses:
CH 123A: Chemistry I
CH 124 A & C: Chemistry I Laboratory
CH 506: Environmental Chemistry
CH 500C: Atomic Absorption Spectroscopy
Spring 2008 Courses:
CH 124 B: Chemistry I Laboratory
CH 376/377: Quantitative Analysis & Laboratory
CH 578: Water Analysis
CH 777: Instrumental Analysis & Laboratory
devices for the quantification of several ionic species. A
polymer membrane gives the electrode its selectivity and is mounted on
the end of the electrode body. In a traditional ion-exchange
membrane, the selectivity is governed by how well the ions partition
into the hydrophobic polymer (called the Hofmeister Series in
anions). Adding an ionophore to the membrane induces a change
in
the selectivity pattern. While
methods for determining cations are well established, several
challenges remain
in the analysis of anions. Our research in this area includes
the
design and synthesis of metal-ligand complexes that selectively bind
anions. Upon adding these complexes to the polymer membranes,
we
observe non-Hofmeister response patterns. Anions of
particular
interest include fluoride, nitrate, nitrite and bromide. The
ultimate goal of this work is to fabricate useful sensor devices for
simple environmental field analysis.
measurements can be cast
onto glass slides and their UV/Vis absorbance properties monitored
with a spectrophotometer. Transition metal complexes are
often
highly colored, and binding of a target analyte can modulate the
absorbance of this ionophore. However, it is also common to
see
little or no change in absorbance of the metal complex upon binding of
analyte. In these cases, a pH sensitive co-ionophore is
incorporated into the sensing film so that the binding event can be
measured. When an anion is selectively extracted from the
aqueous
sample solution into the polymer membrane, a positively charged proton
is co-extracted to maintain charge neutrality. The
co-ionophore's
absorbance properties are sensitive to its protonation state and thus,
upon binding the extracted proton, a color change is observed and this
change can be quantified. Initial experiments involve bathing
the
film within a cuvette and we
will then fabricate a flow-through system in order to quickly measure
environmental samples using this detection scheme.
cannot be used or stored under non-physiological temperature, pH or
solvent. These limitations have led researchers to develop
synthetic analogs of enzymes and antibodies. One approach in
this
area includes molecularly imprinted polymers (MIP).
As
described in the figure, the template is complexed by functional
monomers. This template complex is then copolymerized in the
prescence of excess crosslinker. Template removal yields an
imprinted site containing reactive groups with the capability to rebind
the template selectively in mixtures of structurally similar
molecules. This is a promising strategy, but one difficulty
in
using these materials as sensors is the measurement of a binding
event. The vast majority of MIP research has focused on
utilizing
the materials as selective stationary phases for chromatography and
less work has been done in MIP sensor technology. In this
work we
aim to create polymer membranes on the surface of electrodes by
electropolymerization techniques with a solution of monomers
containing functional monomers and template molecules. We
will
then
attempt to selectively measure the template using cyclic voltammetry as
a means of measurement. Analytes of interest in this study
include a variety of pesticides and herbicides.| ESU Chemistry Department | ESU Dept. of
Physical Science |
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