Home > Seminars > Reilly Lectureship, Lecture 1: Structure, Dynamics and Properties of Block Polymer Dispersions

Reilly Lectureship, Lecture 1: Structure, Dynamics and Properties of Block Polymer Dispersions

Start:

3/25/2014 at 3:30PM

End:

3/25/2014 at 4:30PM

Location:

Eck Center Auditorium

Host:

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Edward Maginn

Edward Maginn

VIEW FULL PROFILE Email: ed@nd.edu
Phone: 574-631-5687
Website: http://www.nd.edu/~ed/
Office: 182A Fitzpatrick Hall

Affiliations

Department of Chemical and Biomolecular Engineering Dorini Family Professor of Energy Studies and Department Chair
College of Engineering Dorini Family Professor of Energy Studies and Chair of the Department of Chemical and Biomolecular Engineering
The research in our group focuses on developing a fundamental understanding of the link between the physical properties of materials and their chemical constitution. Much of our work is devoted to applications related to energy and the environment. The main tool we use is molecular simulation. In ...
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Block copolymers belong to a broad class of amphiphilic compounds that includes soaps, lipids and nonionic surfactants. These macromolecules assemble into micelles with molecular dimensions on the order of 5 to 50 nm in size when mixed with excess solvent that preferentially solvates one block type. This presentation will explore two different aspects of block copolymer micelle formation. The fundamental thermodynamic and kinetic factors that control micelle shape and dynamics will be discussed based on small-angle x-ray and neutron scattering (SAXS and SANS) experiments and cryogenic transmission and scanning electron microscopy results. Although the structural features displayed by amphiphilic block copolymers resemble those associated with the self-assembly of lipids and simple surfactants (e.g., spherical and cylindrical micelles and vesicles) a macromolecular architecture leads to remarkably different dynamic properties, linked to a vanishingly small critical micelle concentration. As a consequence, molecular exchange is rapidly extinguished with increasing molecular weight resulting in non-ergotic behavior. These concepts have been exploited in developing a recently commercialized technology that provides immense improvements in the fracture toughness of thermosetting epoxy plastics, which also will be described.

Seminar Speaker:

Frank S. Bates

Frank S. Bates

University of Minnesota

Frank S. Bates is a Regents Professor and Head of Chemical Engineering and Materials Science at the University of Minnesota. He received a B.S. in Mathematics from SUNY Albany in 1976, and M.S. and Sc.D. degrees in Chemical Engineering from MIT in 1979 and 1982. Between 1982 and 1989 Bates was a member of the technical staff at AT&T Bell Laboratories then joined the University of Minnesota as an Associate Professor. He was promoted to Professor in 1991, named a Distinguished McKnight University Professor in 1996, appointed Department Head in 1999, and became a Regents Professor in 2007. Professor Bates conducts research on a range of topics related to polymers, with a particular focus on the thermodynamics and dynamics of block polymers and blends. In 1988 Bates was named a Distinguished Member of the Technical Staff at Bell Labs. In 1989 he received the John H. Dillon Medal and in 1997 the Polymer Physics Prize, both from the American Physical Society where he is a Fellow. He received the 2004 David Turnbull Lectureship Award from the Materials Research Society, shared the ACS Cooperative Research Award in 2008, was awarded the 2008 Sustained Research Prize by the Neutron Scattering Society of America and he was the 2012 Institute Lecturer of the American Institute of Chemical Engineers. Bates was elected to the US National Academy of Engineering in 2002. In 2005 he was named a fellow of the American Association for the Advancement of Science and in 2010 was elected to the American Academy of Arts and Science.
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