<?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>2026-09-23T16:57:38Z</responseDate><request verb="GetRecord" identifier="oai:dspace.mit.edu:1721.1/8792" metadataPrefix="dim">https://dspace.mit.edu/server/oai/request</request><GetRecord><record><header><identifier>oai:dspace.mit.edu:1721.1/8792</identifier><datestamp>2022-01-13T07:54:23Z</datestamp><setSpec>com_1721.1_7582</setSpec><setSpec>com_1721.1_7581</setSpec><setSpec>col_1721.1_131023</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">John T. Germaine.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="author" lang="en_US">Hwang, Grace Mei-Hua, 1972-</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="other" lang="en_US">Massachusetts Institute of Technology. Dept. of Civil and Environmental Engineering.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="department">Massachusetts Institute of Technology. Department of Civil and Environmental Engineering</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="accessioned">2005-08-23T15:22:18Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="available">2005-08-23T15:22:18Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="issued" lang="en_US">1998</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="uri">http://hdl.handle.net/1721.1/8792</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="oclc" lang="en_US">48198136</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Thesis (S.M.)--Massachusetts Institute of Technology, Dept. of Civil and Environmental Engineering, 1998.</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">"February 1998."</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Includes bibliographical references.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract" lang="en_US">This thesis presents a feasibility study that validates the pursuit of a field inorganic chemical analysis instrument. The instrument envisioned will have commercial marketability, and the study will enhance the understanding of fundamental science, and improve the practicable implementation of environmental policy and regulation. A novel, rapid, micro-Laser Induced Breakdown Spectroscopy ([mu]LIBS) technique for inorganic identification has been explored in metals, metal alloys, soil and paint pellets. This study employed a passively Q-switched infrared Microchip laser, in conjunction with a time-integrated miniature charged-couple device array spectrometer. During the period of this research, the Microchip laser was available only through MIT Lincoln Laboratory. The unique features of the Microchip Laser, (i.e., high peak power, short pulse width, miniaturization), make it a practical excitation source for chemical analysis. Its high pulse rate yields inherent spectra averaging. It's short pulse width and small focal size leads to a rapidly quenched µLIB plasma, which does not develop signal-dominating thermal radiation. Results from this study demonstrated a repeatable correlation between analyte signal strength at indicative emission wavelengths (i.e., lines) as a function of analyte concentration, for lead in metal alloys. A minimum detection limit of 0.07 % was observed for Lead in Leaded Copper. Quantitative detection limits of about 0.06 % for Lead was observed in Lead-Tin solders. All aforementioned detection limits were obtained without the use of any time-gating detectors. This technique was also used to demonstrate ionic lead and numerous other inorganic composition of soil and lead-in-paint. The work presented in this thesis demonstrates that [mu]LIBS is a practical means of detecting metal concentration in a variety of substrates. This thesis provides technical validation for the continued research to fully explore the applicability of the [mu]LIBS technique, as a multi-element inorganic detection tool for solid and aqueous environmental media.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="statementofresponsibility" lang="en_US">by Grace Mei-Hua Hwang.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="degree" lang="en_US">S.M.</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 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">http://dspace.mit.edu/handle/1721.1/7582</dim:field>
   <dim:field mdschema="dc" element="subject" lang="en_US">Civil and Environmental Engineering.</dim:field>
   <dim:field mdschema="dc" element="title" lang="en_US">Feasibility study of micro-laser induced breakdown spectroscopy applied to lead identification in metal alloys and environmental matrices</dim:field>
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   	&lt;Title>Feasibility study of micro-laser induced breakdown spectroscopy applied to lead identification in metal alloys and environmental matrices&lt;/Title>
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   	&lt;PublicationDate>1998&lt;/PublicationDate>
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        	&lt;DisplayName>Hwang, Grace Mei-Hua, 1972-&lt;/DisplayName>
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    &lt;Keyword>Civil and Environmental Engineering.&lt;/Keyword>
   	&lt;Abstract>This thesis presents a feasibility study that validates the pursuit of a field inorganic chemical analysis instrument. The instrument envisioned will have commercial marketability, and the study will enhance the understanding of fundamental science, and improve the practicable implementation of environmental policy and regulation. A novel, rapid, micro-Laser Induced Breakdown Spectroscopy ([mu]LIBS) technique for inorganic identification has been explored in metals, metal alloys, soil and paint pellets. This study employed a passively Q-switched infrared Microchip laser, in conjunction with a time-integrated miniature charged-couple device array spectrometer. During the period of this research, the Microchip laser was available only through MIT Lincoln Laboratory. The unique features of the Microchip Laser, (i.e., high peak power, short pulse width, miniaturization), make it a practical excitation source for chemical analysis. Its high pulse rate yields inherent spectra averaging. It&amp;apos;s short pulse width and small focal size leads to a rapidly quenched µLIB plasma, which does not develop signal-dominating thermal radiation. Results from this study demonstrated a repeatable correlation between analyte signal strength at indicative emission wavelengths (i.e., lines) as a function of analyte concentration, for lead in metal alloys. A minimum detection limit of 0.07 % was observed for Lead in Leaded Copper. Quantitative detection limits of about 0.06 % for Lead was observed in Lead-Tin solders. All aforementioned detection limits were obtained without the use of any time-gating detectors. This technique was also used to demonstrate ionic lead and numerous other inorganic composition of soil and lead-in-paint. The work presented in this thesis demonstrates that [mu]LIBS is a practical means of detecting metal concentration in a variety of substrates. This thesis provides technical validation for the continued research to fully explore the applicability of the [mu]LIBS technique, as a multi-element inorganic detection tool for solid and aqueous environmental media.&lt;/Abstract>
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