<?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>2026-09-19T02:20:12Z</responseDate><request verb="GetRecord" identifier="oai:dspace.mit.edu:1721.1/70397" metadataPrefix="dim">https://dspace.mit.edu/server/oai/request</request><GetRecord><record><header><identifier>oai:dspace.mit.edu:1721.1/70397</identifier><datestamp>2022-01-13T07:54:19Z</datestamp><setSpec>com_1721.1_7582</setSpec><setSpec>com_1721.1_7581</setSpec><setSpec>col_1721.1_131022</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">Robert E. Cohen and Michael F. Rubner.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="author" lang="en_US">DeRocher, Jonathan P</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="other" lang="en_US">Massachusetts Institute of Technology. Dept. of Chemical Engineering.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="department">Massachusetts Institute of Technology. Department of Chemical Engineering</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="accessioned">2012-04-26T18:49:44Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="available">2012-04-26T18:49:44Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="copyright" lang="en_US">2011</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="issued" lang="en_US">2011</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="uri">http://hdl.handle.net/1721.1/70397</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="oclc" lang="en_US">783860895</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Chemical Engineering, 2011.</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 (p. 142-149).</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract" lang="en_US">The fundamental nature of layer-by-layer (LbL) assembly in confined geometries was investigated for a number of different chemical systems. The first part of this thesis concerns the modification of microfluidic and nanofluidic devices which hold great potential as a platform for manipulation and analysis of small sample volumes. The high throughput and high surface area possible with these devices suggests applications in biomolecule or chemical detection, selective separation, and heterogeneous catalysis. To realize some of this potential, the surfaces of these devices can be modified to impart functionality to the device. Polyelectrolyte multilayers can be used to impart a broad array of novel functionalities to a surface including stimuli-responsiveness, reversible switching of the gap thickness, manipulation of the sign and/or the density of the surface charge, chemical functionality and wettability of a surface. Polymer/polymer, polymer/nanoparticle, and nanoparticle/nanoparticle multilayers have all been deposited in confined channels. In all cases, conformal uniform multilayers were observed throughout the high aspect ratio channel. LbL assembly within submicron channels does, however, reveal a number of interesting departures from what is seen for LbL growth on infinite planar surfaces and we explain this effect by surface charge-induced depletion of the adsorbing species in the confined channel at each stage of the assembly process. At sufficiently low ionic strengths, this exclusion prevents further deposition on confined surfaces while adjacent unconfined surfaces continue to be coated. Nanoparticle/nanoparticle deposition results in systematic bridging of the nanochannels with a nanoporous multilayer. This fundamental knowledge was applied to the systematic narrowing of nanochannels embedded in a hybrid micro/nanofluidic device using LbL assembly of polyelectrolytes. The narrowing of these channels was monitored using conductance experiments and showed that the channel thickness could be controlled down to 11 nm. Understanding of exclusion was used to modify track etched polycarbonate membranes in an attempt to build composite membranes which exhibited high salt rejection and high water permeance. These membranes were compared with theoretical models and with commercially available reverse osmosis membranes.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="statementofresponsibility" lang="en_US">by Jonathan Paul DeRocher.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="degree" lang="en_US">Ph.D.</dim:field>
   <dim:field mdschema="dc" element="format" qualifier="extent" lang="en_US">164 p.</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">Chemical Engineering.</dim:field>
   <dim:field mdschema="dc" element="title" lang="en_US">Layer-by-layer assembly in confined geometries</dim:field>
   <dim:field mdschema="dc" element="title" qualifier="alternative" lang="en_US">LbL assembly in confined geometries</dim:field>
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   	&lt;Title>Layer-by-layer assembly in confined geometries&lt;/Title>
   	&lt;Subtitle>LbL assembly in confined geometries&lt;/Subtitle>
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   	&lt;PublicationDate>2011&lt;/PublicationDate>
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        	&lt;DisplayName>DeRocher, Jonathan P&lt;/DisplayName>
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    &lt;Keyword>Chemical Engineering.&lt;/Keyword>
   	&lt;Abstract>The fundamental nature of layer-by-layer (LbL) assembly in confined geometries was investigated for a number of different chemical systems. The first part of this thesis concerns the modification of microfluidic and nanofluidic devices which hold great potential as a platform for manipulation and analysis of small sample volumes. The high throughput and high surface area possible with these devices suggests applications in biomolecule or chemical detection, selective separation, and heterogeneous catalysis. To realize some of this potential, the surfaces of these devices can be modified to impart functionality to the device. Polyelectrolyte multilayers can be used to impart a broad array of novel functionalities to a surface including stimuli-responsiveness, reversible switching of the gap thickness, manipulation of the sign and/or the density of the surface charge, chemical functionality and wettability of a surface. Polymer/polymer, polymer/nanoparticle, and nanoparticle/nanoparticle multilayers have all been deposited in confined channels. In all cases, conformal uniform multilayers were observed throughout the high aspect ratio channel. LbL assembly within submicron channels does, however, reveal a number of interesting departures from what is seen for LbL growth on infinite planar surfaces and we explain this effect by surface charge-induced depletion of the adsorbing species in the confined channel at each stage of the assembly process. At sufficiently low ionic strengths, this exclusion prevents further deposition on confined surfaces while adjacent unconfined surfaces continue to be coated. Nanoparticle/nanoparticle deposition results in systematic bridging of the nanochannels with a nanoporous multilayer. This fundamental knowledge was applied to the systematic narrowing of nanochannels embedded in a hybrid micro/nanofluidic device using LbL assembly of polyelectrolytes. The narrowing of these channels was monitored using conductance experiments and showed that the channel thickness could be controlled down to 11 nm. Understanding of exclusion was used to modify track etched polycarbonate membranes in an attempt to build composite membranes which exhibited high salt rejection and high water permeance. These membranes were compared with theoretical models and with commercially available reverse osmosis membranes.&lt;/Abstract>
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