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Covalently bonded polymer films can be formed by graft polymerizing a suitable monomer onto substrate surfaces via the use of free-radical initiators, cationic/anionic initiators, or by using a combination of a catalyst and initiators for controlled graft polymerization. Yet each of these techniques relies on the presence of initiator sites which must be first covalently grafted to the surface by techniques such as silylation, self assembly, or functionalized molecules that act as anchoring sites for monomer grafting. It is noted that in the case of inorganic oxide surfaces, the surface density of initiation sites is limited by the intrinsic availability of native surface hydroxyl groups which typically serve for attaching the active anchoring species to the substrate. Alternative methods of graft polymerization that are based on surface activation via low pressure plasma surface activation have also been developed. However, such approaches are expensive, impractical for large-scale applications and are also difficult to control.
INNOVATION: UCLA researchers have developed a novel process for surface modification of a broad range of inorganic surfaces via atmospheric plasma-induced graft polymerization. The process utilizes atmospheric gas plasma for surface activation with subsequent graft polymerization of the desired vinyl monomers. The presence of the grafted polymer chains on the substrate was confirmed by infrared spectroscopy. Additionally, surface topology and surface feature uniformity was evaluated by Atomic Force Microscopy (AFM).
POTENTIAL APPLICATIONS
ADVANTAGES
Reference: UCLA Case No. 2006-661
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