Role of Specific and Van Der Waals Interactions in Adhesion of Silica MFI Zeolites (010) with Polyimides

Thursday, November 12, 2009: 3:55 PM
Tennessee D (Gaylord Opryland Hotel)

Carson Meredith, School of Chemical and Biomolecular Engineering, Georgia Institute of Technology, Atlanta, GA
Jung-Hyun Lee, School of Chemical and Biomolecular Engineering, Georgia Institute of Technology, Atlanta, GA
Reginald B.J. Thio, School of Chemical and Biomolecular Engineering, Georgia Institute of Technology, Atlanta, GA
Tae-Hyun Bae, School of Chemical and Biomolecular Engineering, Georgia Institute of Technology, Atlanta, GA

Adhesion between zeolites and polymers is a central factor in achieving defect-free mixed-matrix membranes for energy-efficient gas separations. In this work, atomic force microscopy (AFM) was used to measure adhesion forces between a pure silica MFI (ZSM-5: Zeolite Socony Mobil-Five) (010) zeolite probe and a series of polyimide (MatrimidŽ 5218, 6FDA-DAM, 6FDA-6FpDA, and 6FDA-DAM:DABA (3:2)) and polyetherimide (UltemŽ 1000) polymers in air. Combined with measurements of surface energy of the polymer surfaces, the dependence of adhesion on polymer structure was determined. Adhesion force was strongly dependent on the Lewis basicity component of polymer surface energy, and was less dependent on VDW components, by a factor of about 6. Hydrogen bonding likely occurs between the acidic (electron acceptor) component of the zeolite surface (silanols or adsorbed water) and the basic (electron donor) component of the polymer surface. Adhesion force was strongly correlated with the mole fraction of carbonyls per monomer. We conclude that differences in adhesion as a function of polymer structure were primarily controlled by the polymers Lewis basicity, contributed primarily by carbonyl groups.
Extended Abstract: File Not Uploaded
See more of this Session: Polymer Thin Films and Interfaces III
See more of this Group/Topical: Materials Engineering and Sciences Division