Photoreactive functionalization of poly(ethylene terephthalate) track-etched pore surfaces with \"smart\" polymer systems.
In: Macromolecular Chemistry and Physics, Jg. 206 (2005) ; Nr. 2, S. 268-281
Zeitschriftenaufsatz / Fach: Chemie
Poly(ethylene terephthalate) (PET) track-etched membranes with a pore diam. of ca. 700 nm, optionally surface-functionalized to create a \"carboxyl\" or \"amino\" surface, were used for heterogeneous graft copolymns. Grafted poly(acrylic acid) acted as a pH responsive, \"smart\" polymer. To evaluate the surface-specific initiation of graft copolymns. unmodified and primary functionalized membranes were systematically combined with three differently charged benzophenone derivs. as photoinitiators, which were adsorbed on the PET surface prior to the reaction. The functionalized membranes thus obtained were characterized for chem. structure and permeability as a function of pH. The pore structure with a narrow size distribution and the resulting high sensitivity of the membrane permeability to the grafting functionalizations made the track-etched PET membranes a very useful tool for analyzing structure and function of responsive grafted polymer layers. The primary functionalization of the base polymer with a mol. layer of a multifunctional alkylamine (\"amino\" surface) enhanced the efficiency of the subsequent graft copolymn. via photoinitiated hydrogen abstraction considerably because a high d. of well accessible reactive groups had been introduced. The preadsorption of the photoinitiator on the base polymer surface was significantly improved by ionic interactions between the resp. functional groups of the surface and the photoinitiator. Such a photoinitiator preadsorption, esp. when combined with a reactive layer from the primary functionalization, enabled a very efficient and surface selective functionalization because a better control of grafting d. and a redn. of photoinitiated side reactions along with a more efficient use of the photoinitiator were possible.
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