Nanolayer Self-assembly on Ionic Fibers

dc.contributor.advisorOrlando Rojas , Committee Memberen_US
dc.contributor.advisorPeter Hauser, Committee Chairen_US
dc.contributor.advisorStephen Michielsen, Committee Memberen_US
dc.contributor.advisorXiangwu Zhang, Committee Memberen_US
dc.contributor.authorWang, Zhengjiaen_US
dc.date.accessioned2010-04-02T18:56:14Z
dc.date.available2010-04-02T18:56:14Z
dc.date.issued2009-06-19en_US
dc.degree.disciplineFiber and Polymer Scienceen_US
dc.degree.leveldissertationen_US
dc.degree.namePhDen_US
dc.description.abstractThe application of electrostatic self-assembly techniques in textiles has been explored. The layer-by-layer and atomic layer deposition have been used as new methods of textile modification. The use of layer-by-layer and atomic layer deposition offer the possibility of achieving fully conformal, uniform functionalization of textile fibers of any shape. The optimum processing conditions that allow the selective and controlled deposition of organic, inorganic, and metallic substances on textile substrates via self-assembled nanolayers and atomic layer deposition techniques have also been investigated. However, non-uniform surface and irregular shapes in yarns and fibers, especially the natural fibers increase the difficulties of these applications. Recent studies stated the feasibility of using electrostatic self-assembly on cationic cotton substrates. The goal of this research was to determine the charge density on ionic cotton fibers, which directly affect the electrostatic self-assembly. The ionic cotton fabric was produced after treatment of the substrate with a salt of chloroacetic acid or 3-chloro-2-hydroxypropyltrimethyl ammonium chloride. This research also provides a better understanding of layer-by-layer adsorption behaviors of positively or negatively charged polymer solutions on ionic cellulose films as measured by quartz microgravimetry. At neutral solution pH the adsorption of polyelectrolytes on ultrathin cellulose films was found to depend mainly on the charge density of the adsorbing macromolecule and that of the substrates. At the same adsorption condition, the thickness and surface excess (surface concentration) of the adsorbed species are controlled by the nature of the substrate and polyelectrolyte solution.en_US
dc.identifier.otheretd-05042009-162832en_US
dc.identifier.urihttp://www.lib.ncsu.edu/resolver/1840.16/4570
dc.rightsI hereby certify that, if appropriate, I have obtained and attached hereto a written permission statement from the owner(s) of each third party copyrighted matter to be included in my thesis, dis sertation, or project report, allowing distribution as specified below. I certify that the version I submitted is the same as that approved by my advisory committee. I hereby grant to NC State University or its agents the non-exclusive license to archive and make accessible, under the conditions specified below, my thesis, dissertation, or project report in whole or in part in all forms of media, now or hereafter known. I retain all other ownership rights to the copyright of the thesis, dissertation or project report. I also retain the right to use in future works (such as articles or books) all or part of this thesis, dissertation, or project report.en_US
dc.subjectcharge densityen_US
dc.subjectpolyelectrolyte adsorptionen_US
dc.subjectcationic cottonen_US
dc.subjectanionic cottonen_US
dc.subjectQCM-Den_US
dc.titleNanolayer Self-assembly on Ionic Fibersen_US

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