<?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>2026-09-19T14:02:32Z</responseDate><request verb="GetRecord" identifier="oai:dspace.mit.edu:1721.1/89980" metadataPrefix="dim">https://dspace.mit.edu/server/oai/request</request><GetRecord><record><header><identifier>oai:dspace.mit.edu:1721.1/89980</identifier><datestamp>2022-01-13T07:55:22Z</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">Sample, Caitlin (Caitlin Sarah)</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="other" lang="en_US">Massachusetts Institute of Technology. Department 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">2014-09-19T21:32:24Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="available">2014-09-19T21:32:24Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="copyright" lang="en_US">2014</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="issued" lang="en_US">2014</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="uri">http://hdl.handle.net/1721.1/89980</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="oclc" lang="en_US">890129979</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Thesis: S.B., Massachusetts Institute of Technology, Department of Materials Science and Engineering, 2014.</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Cataloged from PDF version of thesis.</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Includes bibliographical references (pages 28-30).</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract" lang="en_US">Hydrogen-bonded multilayer thin films containing tannic acid (TA) and poly(vinyl alcohol) (PVA) were assembled under different pH conditions, and film growth and dissolution behavior was assessed through profilometry. Optimal film growth was achieved at pH 4.0, which contrasted with uncontrollable assembly at lower pH and lack of growth at higher pH. Changes in growth behavior due to variations in the molecular weight and degree of hydrolysis of PVA, as well as the concentration of the two components, were also investigated. High molecular weight PVA resulted in thicker films than low molecular weight PVA in two cases: fully hydrolyzed PVA at a concentration of 1.0 mg/mL and partially hydrolyzed PVA at a concentration of 0.1 mg/mL. In addition, the dynamic adsorption and desorption behavior of these films was investigated using QCM-D. The QCM-D results showed that each polymer immersion step involves both the deposition and removal of mass to and from the system, with the degree of removal determining the extent to which film assembly is successful. The pH stability of the PVA/TA films was higher than other previously investigated PVA based multilayer systems, which is consistent with the high pKa value of TA of 8.5. This increased pH stability, combined with the antioxidant, antimicrobial, antimutagenic, antitumor, and antibacterial properties of TA and the biocompatibility of PVA, makes the PVA/TA system attractive for biomedical applications, including drug delivery and sensing.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="statementofresponsibility" lang="en_US">by Caitlin Sample.</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">30 pages</dim:field>
   <dim:field mdschema="dc" element="language" qualifier="iso" lang="en_US">eng</dim:field>
   <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 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.</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">Hydrogen-bonded layer-by-layer assembly of poly(vinyl alcohol) and tannic acid</dim:field>
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   	&lt;Title>Hydrogen-bonded layer-by-layer assembly of poly(vinyl alcohol) and tannic acid&lt;/Title>
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   	&lt;PublicationDate>2014&lt;/PublicationDate>
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    &lt;Keyword>Materials Science and Engineering.&lt;/Keyword>
   	&lt;Abstract>Hydrogen-bonded multilayer thin films containing tannic acid (TA) and poly(vinyl alcohol) (PVA) were assembled under different pH conditions, and film growth and dissolution behavior was assessed through profilometry. Optimal film growth was achieved at pH 4.0, which contrasted with uncontrollable assembly at lower pH and lack of growth at higher pH. Changes in growth behavior due to variations in the molecular weight and degree of hydrolysis of PVA, as well as the concentration of the two components, were also investigated. High molecular weight PVA resulted in thicker films than low molecular weight PVA in two cases: fully hydrolyzed PVA at a concentration of 1.0 mg/mL and partially hydrolyzed PVA at a concentration of 0.1 mg/mL. In addition, the dynamic adsorption and desorption behavior of these films was investigated using QCM-D. The QCM-D results showed that each polymer immersion step involves both the deposition and removal of mass to and from the system, with the degree of removal determining the extent to which film assembly is successful. The pH stability of the PVA/TA films was higher than other previously investigated PVA based multilayer systems, which is consistent with the high pKa value of TA of 8.5. This increased pH stability, combined with the antioxidant, antimicrobial, antimutagenic, antitumor, and antibacterial properties of TA and the biocompatibility of PVA, makes the PVA/TA system attractive for biomedical applications, including drug delivery and sensing.&lt;/Abstract>
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