<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-09-19T22:33:23Z</responseDate><request verb="GetRecord" identifier="oai:dspace.mit.edu:1721.1/43801" metadataPrefix="dim">https://dspace.mit.edu/server/oai/request</request><GetRecord><record><header><identifier>oai:dspace.mit.edu:1721.1/43801</identifier><datestamp>2022-01-13T07:54:33Z</datestamp><setSpec>com_1721.1_7582</setSpec><setSpec>com_1721.1_7581</setSpec><setSpec>col_1721.1_131024</setSpec></header><metadata><dim:dim xmlns:dim="http://www.dspace.org/xmlns/dspace/dim" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.dspace.org/xmlns/dspace/dim http://www.dspace.org/schema/dim.xsd">
   <dim:field mdschema="dc" element="contributor" qualifier="advisor" lang="en_US">Michael F. Rubner.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="author" lang="en_US">Kunz, Allison (Allison L.)</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="other" lang="en_US">Massachusetts Institute of Technology. Dept. of Materials Science and Engineering.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="department">Massachusetts Institute of Technology. Department of Materials Science and Engineering</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="accessioned">2008-12-11T18:29:46Z</dim:field>
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   <dim:field mdschema="dc" element="date" qualifier="copyright" lang="en_US">2008</dim:field>
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   <dim:field mdschema="dc" element="identifier" qualifier="oclc" lang="en_US">261503975</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Thesis (S.B.)--Massachusetts Institute of Technology, Dept. of Materials Science and Engineering, 2008.</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Includes bibliographical references (leaf [15]).</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract" lang="en_US">This work presents an analysis of surface morphology changes in poly(acrylic acid)/polyacrylamide (PAA/PAAm) hydrogen-bonded multilayers. These changes were induced by immersion of the films in aqueous solutions of poly(allylamine hydrochloride), or PAH, at different levels of pH. Positive charges on PAH are attracted to negative charges on PAA, forming ionic bonds and locally decreasing the hydrophilicity of the multilayer. The degree of ionization for each polyelectrolyte, controlled by the pH of the treatment solution, determines the molecular conformations and the extent of electrostatic interactions. These factors, in turn, determine the resulting morphology of the film. Different surface morphologies appeared in four different pH regimes. Highly acidic solutions retained the film's original smooth surface, but wrinkled, honeycomb, or globular morphologies appeared as the pH increased. The three different surface morphologies correlate with the linear, pearl necklace, and globular conformations of PAH.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="statementofresponsibility" lang="en_US">by Allison Kunz.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="degree" lang="en_US">S.B.</dim:field>
   <dim:field mdschema="dc" element="format" qualifier="extent" lang="en_US">[23] leaves</dim:field>
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   <dim:field mdschema="dc" element="publisher" lang="en_US">Massachusetts Institute of Technology</dim:field>
   <dim:field mdschema="dc" element="rights" lang="en_US">M.I.T. theses are protected by &#xd;
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permission. See provided URL for inquiries about permission.</dim:field>
   <dim:field mdschema="dc" element="rights" qualifier="uri" lang="en_US">http://dspace.mit.edu/handle/1721.1/7582</dim:field>
   <dim:field mdschema="dc" element="subject" lang="en_US">Materials Science and Engineering.</dim:field>
   <dim:field mdschema="dc" element="title" lang="en_US">Characterization of new surface morphologies in a hydrogen-bonded multilayer system</dim:field>
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   	&lt;Title>Characterization of new surface morphologies in a hydrogen-bonded multilayer system&lt;/Title>
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   	&lt;PublicationDate>2008&lt;/PublicationDate>
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        	&lt;DisplayName>Kunz, Allison (Allison L.)&lt;/DisplayName>
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    &lt;Keyword>Materials Science and Engineering.&lt;/Keyword>
   	&lt;Abstract>This work presents an analysis of surface morphology changes in poly(acrylic acid)/polyacrylamide (PAA/PAAm) hydrogen-bonded multilayers. These changes were induced by immersion of the films in aqueous solutions of poly(allylamine hydrochloride), or PAH, at different levels of pH. Positive charges on PAH are attracted to negative charges on PAA, forming ionic bonds and locally decreasing the hydrophilicity of the multilayer. The degree of ionization for each polyelectrolyte, controlled by the pH of the treatment solution, determines the molecular conformations and the extent of electrostatic interactions. These factors, in turn, determine the resulting morphology of the film. Different surface morphologies appeared in four different pH regimes. Highly acidic solutions retained the film&amp;apos;s original smooth surface, but wrinkled, honeycomb, or globular morphologies appeared as the pH increased. The three different surface morphologies correlate with the linear, pearl necklace, and globular conformations of PAH.&lt;/Abstract>
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