<?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>2026-09-18T19:36:27Z</responseDate><request verb="GetRecord" identifier="oai:dspace.mit.edu:1721.1/154356" metadataPrefix="dim">https://dspace.mit.edu/server/oai/request</request><GetRecord><record><header><identifier>oai:dspace.mit.edu:1721.1/154356</identifier><datestamp>2026-06-05T15:56:26Z</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">Issenberg, Phillip</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="author" lang="en_US">Essigmann, John.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="other" lang="en_US">Massachusetts Institute of Technology. Department of Nutrition and Food Science.</dim:field>
   <dim:field mdschema="dc" element="contributor" qualifier="department" lang="en_US">Massachusetts Institute of Technology. Department of Nutrition and Food Science</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="accessioned">2024-04-30T23:57:59Z</dim:field>
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   <dim:field mdschema="dc" element="date" qualifier="issued" lang="en_US">1972</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="uri">https://hdl.handle.net/1721.1/154356</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="oclc" lang="en_US">1393032846</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Thesis: S.M., Massachusetts Institute of Technology, Department of Nutrition and Food Science, 1972</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Cataloged from the official PDF version of thesis.</dim:field>
   <dim:field mdschema="dc" element="description" lang="en_US">Includes bibliographical references (pages 171-180).</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract" lang="en_US">Methods were investigated for determination of volatile nitrosamines which have been reported to occur  in foods and other environmental samples. Nitrosamines were removed from foods using a Likens-Nickerson extractor; 81% of added dimethylnitrosamine and 110% of added diethylnitrosamine were recovered from 10 ng/g spiked aqueous solutions. The factors affecting recovery of these nitrosamines were investigated. The usefulness of Freon-11 as an extracting solvent for nitrosamines was investigated using both batch serial and continuous liquid-liquid extraction. Potential gas chromatographic  (GC) interferences were removed from food extracts by an acid extraction step and, when needed, by liquid column chromatography on alumina and silica gel. Dilute solu­tions containing nitrosamines were analyzed directly  using a GC solvent stripping technique. Nitrosamines  were detected with the Coulson electrolytic conductivity detector operated in the pyrolytic mode and with a flame ionization detector. The sensitivities of these detectors were compared for selected alkyl and heterocyclic nitros­amines. The specificity of the Coulson detector was demonstrated for analysis of extracts of meat and fish samples. Additional clean-up of food extracts is re­quired to insure identification of nitrosamines by combined GC-mass spectrometry. A method employing chromatographic equilibration (frontal analysis) was investigated for determination of dimethylnitrosamine in the air.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="statementofresponsibility" lang="en_US">by John Martin Essigmann.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="degree" lang="en_US">S.M.</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="collection" lang="en_US">S.M. Massachusetts Institute of Technology, Department of Nutrition and Food Science</dim:field>
   <dim:field mdschema="dc" element="format" qualifier="extent" lang="en_US">185 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">MIT theses may be protected by copyright. Please reuse MIT thesis content according to the MIT Libraries Permissions Policy, which is available through the URL provided.</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">Nutrition and Food Science.</dim:field>
   <dim:field mdschema="dc" element="title" lang="en_US">Determination of volatile nitrosamines in foods and other environmental samples</dim:field>
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   	&lt;Title>Determination of volatile nitrosamines in foods and other environmental samples&lt;/Title>
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   	&lt;PublicationDate>1972&lt;/PublicationDate>
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    &lt;Keyword>Nutrition and Food Science.&lt;/Keyword>
   	&lt;Abstract>Methods were investigated for determination of volatile nitrosamines which have been reported to occur  in foods and other environmental samples. Nitrosamines were removed from foods using a Likens-Nickerson extractor; 81% of added dimethylnitrosamine and 110% of added diethylnitrosamine were recovered from 10 ng/g spiked aqueous solutions. The factors affecting recovery of these nitrosamines were investigated. The usefulness of Freon-11 as an extracting solvent for nitrosamines was investigated using both batch serial and continuous liquid-liquid extraction. Potential gas chromatographic  (GC) interferences were removed from food extracts by an acid extraction step and, when needed, by liquid column chromatography on alumina and silica gel. Dilute solu­tions containing nitrosamines were analyzed directly  using a GC solvent stripping technique. Nitrosamines  were detected with the Coulson electrolytic conductivity detector operated in the pyrolytic mode and with a flame ionization detector. The sensitivities of these detectors were compared for selected alkyl and heterocyclic nitros­amines. The specificity of the Coulson detector was demonstrated for analysis of extracts of meat and fish samples. Additional clean-up of food extracts is re­quired to insure identification of nitrosamines by combined GC-mass spectrometry. A method employing chromatographic equilibration (frontal analysis) was investigated for determination of dimethylnitrosamine in the air.&lt;/Abstract>
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