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Thermal degradation kinetics of in situ prepared PET nanocomposites with acid-treated multi-walled carbon nanotubes
A series of PET/acid-treated multi-walled carbon nanotubes (MWCNTs) nanocomposites of varying nanoparticles’ concentration were prepared, using the in situ polymerization technique. TEM micrographs verified that the dispersion of the MWCNTs into the PET matrix was homogeneous, while some relatively...
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Published in: | Journal of thermal analysis and calorimetry 2010-06, Vol.100 (3), p.1063-1071 |
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description | A series of PET/acid-treated multi-walled carbon nanotubes (MWCNTs) nanocomposites of varying nanoparticles’ concentration were prepared, using the in situ polymerization technique. TEM micrographs verified that the dispersion of the MWCNTs into the PET matrix was homogeneous, while some relatively small aggregates co-existed at higher filler contents. Intrinsic viscosity of the prepared nanocomposites was increased at low MWCNTs contents (up to 0.25 wt%), while at higher contents a gradual reduction was observed. The surface carboxylic groups of acid-treated MWCNTs probably reacted with the hydroxyl end groups of PET, acting as chain extenders at smaller concentrations, while at higher concentrations, on the other hand, led to the formation of branched and cross-linked macromolecules, with reduced apparent molecular weights. From the thermogravimetric curves, it was concluded that the prepared samples exhibited good thermostability, since no remarkable mass loss occurred up to 320 °C ( |
doi_str_mv | 10.1007/s10973-009-0426-4 |
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E
) of degradation of the studied materials was estimated using the Ozawa, Flynn, and Wall (OFW), Friedman and Kissinger’s methods. Pure PET had an
E
= 223.5 kJ/mol, while in the PET/MWCNTs nanocomposites containing up to 1 wt% the
E
gradually increased, indicating that MWCNTs had a stabilizing effect upon the decomposition of the matrix. Only the sample containing 2 wt% of MWCNTs exhibited a lower
E
due to the existence of the aforementioned cross-linked macromolecules. The form of the conversion function for all the studied samples obtained by fitting was the mechanism of
n
th-order auto-catalysis.</description><identifier>ISSN: 1388-6150</identifier><identifier>EISSN: 1588-2926</identifier><identifier>EISSN: 1572-8943</identifier><identifier>DOI: 10.1007/s10973-009-0426-4</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Analytical Chemistry ; Applied sciences ; Calorimetry ; Chemistry ; Chemistry and Materials Science ; Composites ; Crosslinking ; Exact sciences and technology ; Fittings ; Forms of application and semi-finished materials ; Hydroxides ; Inorganic Chemistry ; Macromolecules ; Measurement Science and Instrumentation ; Multi wall carbon nanotubes ; Nanocomposites ; Nanotubes ; Physical Chemistry ; Polyethylene terephthalate ; Polyethylene terephthalates ; Polymer industry, paints, wood ; Polymer Sciences ; Polymerization ; Technology of polymers</subject><ispartof>Journal of thermal analysis and calorimetry, 2010-06, Vol.100 (3), p.1063-1071</ispartof><rights>Akadémiai Kiadó, Budapest, Hungary 2009</rights><rights>2015 INIST-CNRS</rights><rights>COPYRIGHT 2010 Springer</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c423t-d326fad7dc19a4ba5e386de1d14781a6998c9cb75a7cfba46ce07dd778c068a3</citedby><cites>FETCH-LOGICAL-c423t-d326fad7dc19a4ba5e386de1d14781a6998c9cb75a7cfba46ce07dd778c068a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=22828960$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Vassiliou, A. A.</creatorcontrib><creatorcontrib>Chrissafis, K.</creatorcontrib><creatorcontrib>Bikiaris, D. N.</creatorcontrib><title>Thermal degradation kinetics of in situ prepared PET nanocomposites with acid-treated multi-walled carbon nanotubes</title><title>Journal of thermal analysis and calorimetry</title><addtitle>J Therm Anal Calorim</addtitle><description>A series of PET/acid-treated multi-walled carbon nanotubes (MWCNTs) nanocomposites of varying nanoparticles’ concentration were prepared, using the in situ polymerization technique. TEM micrographs verified that the dispersion of the MWCNTs into the PET matrix was homogeneous, while some relatively small aggregates co-existed at higher filler contents. Intrinsic viscosity of the prepared nanocomposites was increased at low MWCNTs contents (up to 0.25 wt%), while at higher contents a gradual reduction was observed. The surface carboxylic groups of acid-treated MWCNTs probably reacted with the hydroxyl end groups of PET, acting as chain extenders at smaller concentrations, while at higher concentrations, on the other hand, led to the formation of branched and cross-linked macromolecules, with reduced apparent molecular weights. From the thermogravimetric curves, it was concluded that the prepared samples exhibited good thermostability, since no remarkable mass loss occurred up to 320 °C (<0.5%). The activation energy (
E
) of degradation of the studied materials was estimated using the Ozawa, Flynn, and Wall (OFW), Friedman and Kissinger’s methods. Pure PET had an
E
= 223.5 kJ/mol, while in the PET/MWCNTs nanocomposites containing up to 1 wt% the
E
gradually increased, indicating that MWCNTs had a stabilizing effect upon the decomposition of the matrix. Only the sample containing 2 wt% of MWCNTs exhibited a lower
E
due to the existence of the aforementioned cross-linked macromolecules. The form of the conversion function for all the studied samples obtained by fitting was the mechanism of
n
th-order auto-catalysis.</description><subject>Analytical Chemistry</subject><subject>Applied sciences</subject><subject>Calorimetry</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Composites</subject><subject>Crosslinking</subject><subject>Exact sciences and technology</subject><subject>Fittings</subject><subject>Forms of application and semi-finished materials</subject><subject>Hydroxides</subject><subject>Inorganic Chemistry</subject><subject>Macromolecules</subject><subject>Measurement Science and Instrumentation</subject><subject>Multi wall carbon nanotubes</subject><subject>Nanocomposites</subject><subject>Nanotubes</subject><subject>Physical Chemistry</subject><subject>Polyethylene terephthalate</subject><subject>Polyethylene terephthalates</subject><subject>Polymer industry, paints, wood</subject><subject>Polymer Sciences</subject><subject>Polymerization</subject><subject>Technology of polymers</subject><issn>1388-6150</issn><issn>1588-2926</issn><issn>1572-8943</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNp9kU9rFTEUxQdRsNR-AHfZiLiYmmRm8mdZSq2FgqJvH-4kd16jM8mYZKh-e_OYInQjWeTm3t85hHua5i2jl4xS-TEzqmXXUqpb2nPR9i-aMzYo1XLNxctad7UWbKCvm4uc_Ug5o0IPSp81-fCAaYGZODwmcFB8DOSnD1i8zSROxAeSfdnImnCFhI58vTmQACHauKyxjjCTR18eCFjv2pIQSoWWbS6-fYR5rg8LaayuJ1HZRsxvmlcTzBkvnu7z5vDp5nD9ub3_cnt3fXXf2p53pXUdFxM46SzT0I8wYKeEQ-ZYLxUDobWy2o5yAGmnEXphkUrnpFSWCgXdefN-t11T_LVhLmbx2eI8Q8C4ZaNFp3o6MFbJy508wozGhymWBLYeh4u3MeDka_-qGzSTTHddFXx4JqhMwd_lCFvO5u77t-cs21mbYs4JJ7Mmv0D6Yxg1p_jMHp-p8ZlTfKavmndPX4dsYZ4SBOvzPyHniistaOX4zuU6CkdM5kfcUqhL_Y_5X-LYq3k</recordid><startdate>20100601</startdate><enddate>20100601</enddate><creator>Vassiliou, A. A.</creator><creator>Chrissafis, K.</creator><creator>Bikiaris, D. N.</creator><general>Springer Netherlands</general><general>Springer</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>ISR</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope></search><sort><creationdate>20100601</creationdate><title>Thermal degradation kinetics of in situ prepared PET nanocomposites with acid-treated multi-walled carbon nanotubes</title><author>Vassiliou, A. A. ; Chrissafis, K. ; Bikiaris, D. N.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c423t-d326fad7dc19a4ba5e386de1d14781a6998c9cb75a7cfba46ce07dd778c068a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Analytical Chemistry</topic><topic>Applied sciences</topic><topic>Calorimetry</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Composites</topic><topic>Crosslinking</topic><topic>Exact sciences and technology</topic><topic>Fittings</topic><topic>Forms of application and semi-finished materials</topic><topic>Hydroxides</topic><topic>Inorganic Chemistry</topic><topic>Macromolecules</topic><topic>Measurement Science and Instrumentation</topic><topic>Multi wall carbon nanotubes</topic><topic>Nanocomposites</topic><topic>Nanotubes</topic><topic>Physical Chemistry</topic><topic>Polyethylene terephthalate</topic><topic>Polyethylene terephthalates</topic><topic>Polymer industry, paints, wood</topic><topic>Polymer Sciences</topic><topic>Polymerization</topic><topic>Technology of polymers</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vassiliou, A. A.</creatorcontrib><creatorcontrib>Chrissafis, K.</creatorcontrib><creatorcontrib>Bikiaris, D. N.</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Gale In Context: Science</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Journal of thermal analysis and calorimetry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Vassiliou, A. A.</au><au>Chrissafis, K.</au><au>Bikiaris, D. N.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Thermal degradation kinetics of in situ prepared PET nanocomposites with acid-treated multi-walled carbon nanotubes</atitle><jtitle>Journal of thermal analysis and calorimetry</jtitle><stitle>J Therm Anal Calorim</stitle><date>2010-06-01</date><risdate>2010</risdate><volume>100</volume><issue>3</issue><spage>1063</spage><epage>1071</epage><pages>1063-1071</pages><issn>1388-6150</issn><eissn>1588-2926</eissn><eissn>1572-8943</eissn><abstract>A series of PET/acid-treated multi-walled carbon nanotubes (MWCNTs) nanocomposites of varying nanoparticles’ concentration were prepared, using the in situ polymerization technique. TEM micrographs verified that the dispersion of the MWCNTs into the PET matrix was homogeneous, while some relatively small aggregates co-existed at higher filler contents. Intrinsic viscosity of the prepared nanocomposites was increased at low MWCNTs contents (up to 0.25 wt%), while at higher contents a gradual reduction was observed. The surface carboxylic groups of acid-treated MWCNTs probably reacted with the hydroxyl end groups of PET, acting as chain extenders at smaller concentrations, while at higher concentrations, on the other hand, led to the formation of branched and cross-linked macromolecules, with reduced apparent molecular weights. From the thermogravimetric curves, it was concluded that the prepared samples exhibited good thermostability, since no remarkable mass loss occurred up to 320 °C (<0.5%). The activation energy (
E
) of degradation of the studied materials was estimated using the Ozawa, Flynn, and Wall (OFW), Friedman and Kissinger’s methods. Pure PET had an
E
= 223.5 kJ/mol, while in the PET/MWCNTs nanocomposites containing up to 1 wt% the
E
gradually increased, indicating that MWCNTs had a stabilizing effect upon the decomposition of the matrix. Only the sample containing 2 wt% of MWCNTs exhibited a lower
E
due to the existence of the aforementioned cross-linked macromolecules. The form of the conversion function for all the studied samples obtained by fitting was the mechanism of
n
th-order auto-catalysis.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><doi>10.1007/s10973-009-0426-4</doi><tpages>9</tpages></addata></record> |
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subjects | Analytical Chemistry Applied sciences Calorimetry Chemistry Chemistry and Materials Science Composites Crosslinking Exact sciences and technology Fittings Forms of application and semi-finished materials Hydroxides Inorganic Chemistry Macromolecules Measurement Science and Instrumentation Multi wall carbon nanotubes Nanocomposites Nanotubes Physical Chemistry Polyethylene terephthalate Polyethylene terephthalates Polymer industry, paints, wood Polymer Sciences Polymerization Technology of polymers |
title | Thermal degradation kinetics of in situ prepared PET nanocomposites with acid-treated multi-walled carbon nanotubes |
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