Engineering the microfabrication of layer-by-layer polyelectrolyte assembly

Thesis (Ph.D.)--Massachusetts Institute of Technology, Dept. of Chemical Engineering, 1999. === Includes bibliographical references. === The feasibility of microstructuring polyelectrolyte multilayers has been established by using the layer-by-layer assembly technique in combination with patterned s...

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Main Author: Clark, Sarah L. (Sarah Louise), 1972-
Other Authors: Paula T. Hammond.
Format: Others
Language:English
Published: Massachusetts Institute of Technology 2005
Subjects:
Online Access:http://hdl.handle.net/1721.1/9509
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spelling ndltd-MIT-oai-dspace.mit.edu-1721.1-95092019-07-13T03:12:17Z Engineering the microfabrication of layer-by-layer polyelectrolyte assembly Clark, Sarah L. (Sarah Louise), 1972- Paula T. Hammond. Massachusetts Institute of Technology. Dept. of Chemical Engineering. Massachusetts Institute of Technology. Dept. of Chemical Engineering. Chemical Engineering. Thesis (Ph.D.)--Massachusetts Institute of Technology, Dept. of Chemical Engineering, 1999. Includes bibliographical references. The feasibility of microstructuring polyelectrolyte multilayers has been established by using the layer-by-layer assembly technique in combination with patterned self-assembled monolayers (SAMs). SAMs of a carboxylic acid surface (COOH) and a triethylene glycol surface (EG) were used to promote and resist polyelectrolyte adsorption. respectively. Processing conditions necessary for the selective deposition of both weak and strong polyelectrolytes were established as a function of polyelectrolyte molecular weight. ionic content, ion type. and pH. Low molecular weight polyelectrolytes adsorbed more selectively on patterned SAM surfaces than high molecular weight polyelectrolytes. Strong polyelectrolytes multilayers of sulfonated poly(styrene) (SPS) and polydiallyldimethyl ammonium chloride (PDAC) required the addition of 0.1 M NaCl to the polyelectrolyte dipping solutions to optimize selective deposition. Adding 1.0 M NaCl to each polyelectrolyte solution and including a periodic drying step in the multilayer fabrication process reversed the templating ability of the COOH and EG SAMs for the SPS/PDAC multilayers. Weak polyelectrolytes such as linear (polyethylenimine) (LPEI), branched (polyethylenimine) (BPEI), poly(allylamine hydrochloride (PAH), poly(acrylic acid) (PAA) and poly(methacrylic acid) (PMAA) were adsorbed at pH 2.5. 4.8, 7, and IO on patterned COOH and EG SAMs to determine optimal patterned deposition conditions. Each polyacid and polyamine had a secondary interaction that changed the affinity of the multi layers for the COOH and EG surfaces. The technique was also extended to include an optically active dye in the multilayers. Imaging the patterned dye multilaycrs under a fluorescence microscope produced light emission from the selectively adsorbed dye molecules. The different conditions and interactions that produced selective deposition of polyelectrolyte multilayers were combined to build complex multilayer structures. A cladding structure was produced by depositing a blanketing layer of strong polyelectrolytes on preformed patterned multilayers. A different complex structure of polyelectrolytes was fabricated by selectively adsorbing a second polyelectrolyte system within the patterned structure of strong polyelectrolyte multilayers. This assembly was accomplished by utilizing secondary interactions of weak polyelectrolyte multilayers with the EG surface. by Sarah L. Clark. Ph.D. 2005-08-22T18:54:54Z 2005-08-22T18:54:54Z 1999 1999 Thesis http://hdl.handle.net/1721.1/9509 43714622 eng M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission. http://dspace.mit.edu/handle/1721.1/7582 187 leaves 18930614 bytes 18930373 bytes application/pdf application/pdf application/pdf Massachusetts Institute of Technology
collection NDLTD
language English
format Others
sources NDLTD
topic Chemical Engineering.
spellingShingle Chemical Engineering.
Clark, Sarah L. (Sarah Louise), 1972-
Engineering the microfabrication of layer-by-layer polyelectrolyte assembly
description Thesis (Ph.D.)--Massachusetts Institute of Technology, Dept. of Chemical Engineering, 1999. === Includes bibliographical references. === The feasibility of microstructuring polyelectrolyte multilayers has been established by using the layer-by-layer assembly technique in combination with patterned self-assembled monolayers (SAMs). SAMs of a carboxylic acid surface (COOH) and a triethylene glycol surface (EG) were used to promote and resist polyelectrolyte adsorption. respectively. Processing conditions necessary for the selective deposition of both weak and strong polyelectrolytes were established as a function of polyelectrolyte molecular weight. ionic content, ion type. and pH. Low molecular weight polyelectrolytes adsorbed more selectively on patterned SAM surfaces than high molecular weight polyelectrolytes. Strong polyelectrolytes multilayers of sulfonated poly(styrene) (SPS) and polydiallyldimethyl ammonium chloride (PDAC) required the addition of 0.1 M NaCl to the polyelectrolyte dipping solutions to optimize selective deposition. Adding 1.0 M NaCl to each polyelectrolyte solution and including a periodic drying step in the multilayer fabrication process reversed the templating ability of the COOH and EG SAMs for the SPS/PDAC multilayers. Weak polyelectrolytes such as linear (polyethylenimine) (LPEI), branched (polyethylenimine) (BPEI), poly(allylamine hydrochloride (PAH), poly(acrylic acid) (PAA) and poly(methacrylic acid) (PMAA) were adsorbed at pH 2.5. 4.8, 7, and IO on patterned COOH and EG SAMs to determine optimal patterned deposition conditions. Each polyacid and polyamine had a secondary interaction that changed the affinity of the multi layers for the COOH and EG surfaces. The technique was also extended to include an optically active dye in the multilayers. Imaging the patterned dye multilaycrs under a fluorescence microscope produced light emission from the selectively adsorbed dye molecules. The different conditions and interactions that produced selective deposition of polyelectrolyte multilayers were combined to build complex multilayer structures. A cladding structure was produced by depositing a blanketing layer of strong polyelectrolytes on preformed patterned multilayers. A different complex structure of polyelectrolytes was fabricated by selectively adsorbing a second polyelectrolyte system within the patterned structure of strong polyelectrolyte multilayers. This assembly was accomplished by utilizing secondary interactions of weak polyelectrolyte multilayers with the EG surface. === by Sarah L. Clark. === Ph.D.
author2 Paula T. Hammond.
author_facet Paula T. Hammond.
Clark, Sarah L. (Sarah Louise), 1972-
author Clark, Sarah L. (Sarah Louise), 1972-
author_sort Clark, Sarah L. (Sarah Louise), 1972-
title Engineering the microfabrication of layer-by-layer polyelectrolyte assembly
title_short Engineering the microfabrication of layer-by-layer polyelectrolyte assembly
title_full Engineering the microfabrication of layer-by-layer polyelectrolyte assembly
title_fullStr Engineering the microfabrication of layer-by-layer polyelectrolyte assembly
title_full_unstemmed Engineering the microfabrication of layer-by-layer polyelectrolyte assembly
title_sort engineering the microfabrication of layer-by-layer polyelectrolyte assembly
publisher Massachusetts Institute of Technology
publishDate 2005
url http://hdl.handle.net/1721.1/9509
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