Loading…

Molecular dynamics of fully biobased poly(butylene 2,5-furanoate) as revealed by broadband dielectric spectroscopy

This work presents the molecular dynamics of both fully amorphous and semicrystalline poly(butylene 2,5-furanoate) (PBF). Broadband dielectric spectroscopy experiments were combined with temperature modulated differential scanning calorimetry measurements. The results showed that the subglass molecu...

Full description

Saved in:
Bibliographic Details
Published in:Polymer (Guilford) 2017-10, Vol.128, p.24-30
Main Authors: Soccio, Michelina, Martínez-Tong, Daniel E., Alegría, Angel, Munari, Andrea, Lotti, Nadia
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c384t-1ab6acdc255e922cbec12b25825613b12d3e0f2ee92bd1fce7683e4f13dbad0d3
cites cdi_FETCH-LOGICAL-c384t-1ab6acdc255e922cbec12b25825613b12d3e0f2ee92bd1fce7683e4f13dbad0d3
container_end_page 30
container_issue
container_start_page 24
container_title Polymer (Guilford)
container_volume 128
creator Soccio, Michelina
Martínez-Tong, Daniel E.
Alegría, Angel
Munari, Andrea
Lotti, Nadia
description This work presents the molecular dynamics of both fully amorphous and semicrystalline poly(butylene 2,5-furanoate) (PBF). Broadband dielectric spectroscopy experiments were combined with temperature modulated differential scanning calorimetry measurements. The results showed that the subglass molecular dynamics is characterized by the existence of two dielectric relaxation processes, being the faster one associated to the glycolic subunit, whereas the slower relaxation was assigned to the link in between the ester group and the furan ring. Crystallization affected differently the contribution of these two components. Additionally, crystallization had a stronger effect on the α relaxation process, related to the segmental dynamics of the amorphous phase. In the semicrystalline state, the PBF amorphous phase was described as being composed by different fractions, including a completely rigid one, with distinctly slower mobilities and reduced contributions to the dielectric relaxation, compared to the fully amorphous polymer. [Display omitted] •Local and segmental dynamics of poly(butylene 2,5-furanoate) (PBF) were studied.•Local dynamics showed a broad relaxation, described by two processes respectively related to the more mobile subunit and to the stiffer moiety.•Amorphous phase mobility depended on the glycol subunit length, while the fragility was mainly correlated to the acid moiety.•Cold crystallization led to a slowdown of the segmental dynamics and concomitant reduced dielectric relaxation strength.•The amorphous phase of semicrystalline PBF was described using different fractions, including a completely rigid fraction.
doi_str_mv 10.1016/j.polymer.2017.09.007
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_1967364195</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0032386117308698</els_id><sourcerecordid>1967364195</sourcerecordid><originalsourceid>FETCH-LOGICAL-c384t-1ab6acdc255e922cbec12b25825613b12d3e0f2ee92bd1fce7683e4f13dbad0d3</originalsourceid><addsrcrecordid>eNqFUMlKBDEQDaLgOPoJQsCLgt1m6fUkMrjBiBc9hywVSNPTaZNuof_eDDN3T1VQb6n3ELqmJKeEVg9dPvp-2UHIGaF1TtqckPoErWhT84yxlp6iFSGcZbyp6Dm6iLEjhLCSFSsUPnwPeu5lwGYZ5M7piL3Fdu77BSvnlYxg8F7_Vs3T0sMAmN2XmZ2DHLyc4A7LiAP8guwTUCVS8NIoORhsHCTtKTiN47hffNR-XC7RmZV9hKvjXKPvl-evzVu2_Xx93zxtM82bYsqoVJXURrOyhJYxrUBTpljZsLKiXFFmOBDLIB2VoVZDXTUcCkt5cjfE8DW6OeiOwf_MECfR-TkMyVLQtqp5VdC2TKjygNLpvRjAijG4nQyLoETs6xWdONYr9vUK0opUb-I9HniQIvy6dI3awaDBuJCyCuPdPwp_i1CJCg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1967364195</pqid></control><display><type>article</type><title>Molecular dynamics of fully biobased poly(butylene 2,5-furanoate) as revealed by broadband dielectric spectroscopy</title><source>ScienceDirect Journals</source><creator>Soccio, Michelina ; Martínez-Tong, Daniel E. ; Alegría, Angel ; Munari, Andrea ; Lotti, Nadia</creator><creatorcontrib>Soccio, Michelina ; Martínez-Tong, Daniel E. ; Alegría, Angel ; Munari, Andrea ; Lotti, Nadia</creatorcontrib><description>This work presents the molecular dynamics of both fully amorphous and semicrystalline poly(butylene 2,5-furanoate) (PBF). Broadband dielectric spectroscopy experiments were combined with temperature modulated differential scanning calorimetry measurements. The results showed that the subglass molecular dynamics is characterized by the existence of two dielectric relaxation processes, being the faster one associated to the glycolic subunit, whereas the slower relaxation was assigned to the link in between the ester group and the furan ring. Crystallization affected differently the contribution of these two components. Additionally, crystallization had a stronger effect on the α relaxation process, related to the segmental dynamics of the amorphous phase. In the semicrystalline state, the PBF amorphous phase was described as being composed by different fractions, including a completely rigid one, with distinctly slower mobilities and reduced contributions to the dielectric relaxation, compared to the fully amorphous polymer. [Display omitted] •Local and segmental dynamics of poly(butylene 2,5-furanoate) (PBF) were studied.•Local dynamics showed a broad relaxation, described by two processes respectively related to the more mobile subunit and to the stiffer moiety.•Amorphous phase mobility depended on the glycol subunit length, while the fragility was mainly correlated to the acid moiety.•Cold crystallization led to a slowdown of the segmental dynamics and concomitant reduced dielectric relaxation strength.•The amorphous phase of semicrystalline PBF was described using different fractions, including a completely rigid fraction.</description><identifier>ISSN: 0032-3861</identifier><identifier>EISSN: 1873-2291</identifier><identifier>DOI: 10.1016/j.polymer.2017.09.007</identifier><language>eng</language><publisher>Kidlington: Elsevier Ltd</publisher><subject>Broadband ; Broadband dielectric spectroscopy ; Calorimetry ; Crystallization ; Dielectric relaxation ; Differential scanning calorimetry ; Molecular dynamics ; Poly(butylene 2,5-furanoate) ; Rigid amorphous fraction ; Semicrystalline polymers ; Spectroscopy ; Thermal analysis</subject><ispartof>Polymer (Guilford), 2017-10, Vol.128, p.24-30</ispartof><rights>2017 Elsevier Ltd</rights><rights>Copyright Elsevier BV Oct 16, 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c384t-1ab6acdc255e922cbec12b25825613b12d3e0f2ee92bd1fce7683e4f13dbad0d3</citedby><cites>FETCH-LOGICAL-c384t-1ab6acdc255e922cbec12b25825613b12d3e0f2ee92bd1fce7683e4f13dbad0d3</cites><orcidid>0000-0002-6437-1658 ; 0000-0002-3115-6222</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Soccio, Michelina</creatorcontrib><creatorcontrib>Martínez-Tong, Daniel E.</creatorcontrib><creatorcontrib>Alegría, Angel</creatorcontrib><creatorcontrib>Munari, Andrea</creatorcontrib><creatorcontrib>Lotti, Nadia</creatorcontrib><title>Molecular dynamics of fully biobased poly(butylene 2,5-furanoate) as revealed by broadband dielectric spectroscopy</title><title>Polymer (Guilford)</title><description>This work presents the molecular dynamics of both fully amorphous and semicrystalline poly(butylene 2,5-furanoate) (PBF). Broadband dielectric spectroscopy experiments were combined with temperature modulated differential scanning calorimetry measurements. The results showed that the subglass molecular dynamics is characterized by the existence of two dielectric relaxation processes, being the faster one associated to the glycolic subunit, whereas the slower relaxation was assigned to the link in between the ester group and the furan ring. Crystallization affected differently the contribution of these two components. Additionally, crystallization had a stronger effect on the α relaxation process, related to the segmental dynamics of the amorphous phase. In the semicrystalline state, the PBF amorphous phase was described as being composed by different fractions, including a completely rigid one, with distinctly slower mobilities and reduced contributions to the dielectric relaxation, compared to the fully amorphous polymer. [Display omitted] •Local and segmental dynamics of poly(butylene 2,5-furanoate) (PBF) were studied.•Local dynamics showed a broad relaxation, described by two processes respectively related to the more mobile subunit and to the stiffer moiety.•Amorphous phase mobility depended on the glycol subunit length, while the fragility was mainly correlated to the acid moiety.•Cold crystallization led to a slowdown of the segmental dynamics and concomitant reduced dielectric relaxation strength.•The amorphous phase of semicrystalline PBF was described using different fractions, including a completely rigid fraction.</description><subject>Broadband</subject><subject>Broadband dielectric spectroscopy</subject><subject>Calorimetry</subject><subject>Crystallization</subject><subject>Dielectric relaxation</subject><subject>Differential scanning calorimetry</subject><subject>Molecular dynamics</subject><subject>Poly(butylene 2,5-furanoate)</subject><subject>Rigid amorphous fraction</subject><subject>Semicrystalline polymers</subject><subject>Spectroscopy</subject><subject>Thermal analysis</subject><issn>0032-3861</issn><issn>1873-2291</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNqFUMlKBDEQDaLgOPoJQsCLgt1m6fUkMrjBiBc9hywVSNPTaZNuof_eDDN3T1VQb6n3ELqmJKeEVg9dPvp-2UHIGaF1TtqckPoErWhT84yxlp6iFSGcZbyp6Dm6iLEjhLCSFSsUPnwPeu5lwGYZ5M7piL3Fdu77BSvnlYxg8F7_Vs3T0sMAmN2XmZ2DHLyc4A7LiAP8guwTUCVS8NIoORhsHCTtKTiN47hffNR-XC7RmZV9hKvjXKPvl-evzVu2_Xx93zxtM82bYsqoVJXURrOyhJYxrUBTpljZsLKiXFFmOBDLIB2VoVZDXTUcCkt5cjfE8DW6OeiOwf_MECfR-TkMyVLQtqp5VdC2TKjygNLpvRjAijG4nQyLoETs6xWdONYr9vUK0opUb-I9HniQIvy6dI3awaDBuJCyCuPdPwp_i1CJCg</recordid><startdate>20171016</startdate><enddate>20171016</enddate><creator>Soccio, Michelina</creator><creator>Martínez-Tong, Daniel E.</creator><creator>Alegría, Angel</creator><creator>Munari, Andrea</creator><creator>Lotti, Nadia</creator><general>Elsevier Ltd</general><general>Elsevier BV</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7QF</scope><scope>7QO</scope><scope>7QQ</scope><scope>7SC</scope><scope>7SE</scope><scope>7SP</scope><scope>7SR</scope><scope>7T7</scope><scope>7TA</scope><scope>7TB</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>H8G</scope><scope>JG9</scope><scope>JQ2</scope><scope>KR7</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope><scope>P64</scope><orcidid>https://orcid.org/0000-0002-6437-1658</orcidid><orcidid>https://orcid.org/0000-0002-3115-6222</orcidid></search><sort><creationdate>20171016</creationdate><title>Molecular dynamics of fully biobased poly(butylene 2,5-furanoate) as revealed by broadband dielectric spectroscopy</title><author>Soccio, Michelina ; Martínez-Tong, Daniel E. ; Alegría, Angel ; Munari, Andrea ; Lotti, Nadia</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c384t-1ab6acdc255e922cbec12b25825613b12d3e0f2ee92bd1fce7683e4f13dbad0d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Broadband</topic><topic>Broadband dielectric spectroscopy</topic><topic>Calorimetry</topic><topic>Crystallization</topic><topic>Dielectric relaxation</topic><topic>Differential scanning calorimetry</topic><topic>Molecular dynamics</topic><topic>Poly(butylene 2,5-furanoate)</topic><topic>Rigid amorphous fraction</topic><topic>Semicrystalline polymers</topic><topic>Spectroscopy</topic><topic>Thermal analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Soccio, Michelina</creatorcontrib><creatorcontrib>Martínez-Tong, Daniel E.</creatorcontrib><creatorcontrib>Alegría, Angel</creatorcontrib><creatorcontrib>Munari, Andrea</creatorcontrib><creatorcontrib>Lotti, Nadia</creatorcontrib><collection>CrossRef</collection><collection>Aluminium Industry Abstracts</collection><collection>Biotechnology Research Abstracts</collection><collection>Ceramic Abstracts</collection><collection>Computer and Information Systems Abstracts</collection><collection>Corrosion Abstracts</collection><collection>Electronics &amp; Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Materials Business File</collection><collection>Mechanical &amp; Transportation Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ANTE: Abstracts in New Technology &amp; Engineering</collection><collection>Engineering Research Database</collection><collection>Aerospace Database</collection><collection>Copper Technical Reference Library</collection><collection>Materials Research Database</collection><collection>ProQuest Computer Science Collection</collection><collection>Civil Engineering Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Computer and Information Systems Abstracts – Academic</collection><collection>Computer and Information Systems Abstracts Professional</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Polymer (Guilford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Soccio, Michelina</au><au>Martínez-Tong, Daniel E.</au><au>Alegría, Angel</au><au>Munari, Andrea</au><au>Lotti, Nadia</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Molecular dynamics of fully biobased poly(butylene 2,5-furanoate) as revealed by broadband dielectric spectroscopy</atitle><jtitle>Polymer (Guilford)</jtitle><date>2017-10-16</date><risdate>2017</risdate><volume>128</volume><spage>24</spage><epage>30</epage><pages>24-30</pages><issn>0032-3861</issn><eissn>1873-2291</eissn><abstract>This work presents the molecular dynamics of both fully amorphous and semicrystalline poly(butylene 2,5-furanoate) (PBF). Broadband dielectric spectroscopy experiments were combined with temperature modulated differential scanning calorimetry measurements. The results showed that the subglass molecular dynamics is characterized by the existence of two dielectric relaxation processes, being the faster one associated to the glycolic subunit, whereas the slower relaxation was assigned to the link in between the ester group and the furan ring. Crystallization affected differently the contribution of these two components. Additionally, crystallization had a stronger effect on the α relaxation process, related to the segmental dynamics of the amorphous phase. In the semicrystalline state, the PBF amorphous phase was described as being composed by different fractions, including a completely rigid one, with distinctly slower mobilities and reduced contributions to the dielectric relaxation, compared to the fully amorphous polymer. [Display omitted] •Local and segmental dynamics of poly(butylene 2,5-furanoate) (PBF) were studied.•Local dynamics showed a broad relaxation, described by two processes respectively related to the more mobile subunit and to the stiffer moiety.•Amorphous phase mobility depended on the glycol subunit length, while the fragility was mainly correlated to the acid moiety.•Cold crystallization led to a slowdown of the segmental dynamics and concomitant reduced dielectric relaxation strength.•The amorphous phase of semicrystalline PBF was described using different fractions, including a completely rigid fraction.</abstract><cop>Kidlington</cop><pub>Elsevier Ltd</pub><doi>10.1016/j.polymer.2017.09.007</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-6437-1658</orcidid><orcidid>https://orcid.org/0000-0002-3115-6222</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0032-3861
ispartof Polymer (Guilford), 2017-10, Vol.128, p.24-30
issn 0032-3861
1873-2291
language eng
recordid cdi_proquest_journals_1967364195
source ScienceDirect Journals
subjects Broadband
Broadband dielectric spectroscopy
Calorimetry
Crystallization
Dielectric relaxation
Differential scanning calorimetry
Molecular dynamics
Poly(butylene 2,5-furanoate)
Rigid amorphous fraction
Semicrystalline polymers
Spectroscopy
Thermal analysis
title Molecular dynamics of fully biobased poly(butylene 2,5-furanoate) as revealed by broadband dielectric spectroscopy
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-05T09%3A04%3A16IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Molecular%20dynamics%20of%20fully%20biobased%20poly(butylene%202,5-furanoate)%20as%20revealed%20by%20broadband%20dielectric%20spectroscopy&rft.jtitle=Polymer%20(Guilford)&rft.au=Soccio,%20Michelina&rft.date=2017-10-16&rft.volume=128&rft.spage=24&rft.epage=30&rft.pages=24-30&rft.issn=0032-3861&rft.eissn=1873-2291&rft_id=info:doi/10.1016/j.polymer.2017.09.007&rft_dat=%3Cproquest_cross%3E1967364195%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c384t-1ab6acdc255e922cbec12b25825613b12d3e0f2ee92bd1fce7683e4f13dbad0d3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1967364195&rft_id=info:pmid/&rfr_iscdi=true