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Thermal and rheological behaviours of some random aromatic amino-ended polyethersulfone/polyetherethersulfone copolymers
The thermal and rheological characterizations of seven random, low molecular weight ( M n ≅ 9500 g mol −1), H 2N-ended polyethersulfone/polyetherethersulfone (PES/PEES) copolymers, at various PES/PEES ratios, were performed. The glass transition temperatures ( T g) were determined by DSC. Degradatio...
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Published in: | Polymer degradation and stability 2006-12, Vol.91 (12), p.3230-3236 |
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creator | Abate, Lorenzo Blanco, Ignazio Cicala, Gianluca Recca, Antonino Restuccia, Carmelo Luca |
description | The thermal and rheological characterizations of seven random, low molecular weight (
M
n
≅
9500
g
mol
−1), H
2N-ended polyethersulfone/polyetherethersulfone (PES/PEES) copolymers, at various PES/PEES ratios, were performed. The glass transition temperatures (
T
g) were determined by DSC. Degradations were carried out in a thermobalance, under flowing nitrogen, in dynamic heating conditions from 35
°C to 650
°C. The initial decomposition temperatures (
T
i) and the half decomposition temperatures (
T
1/2) were directly determined by TG curves, while the apparent activation energies of degradation (
E
a) were obtained by the Kissinger method. In addition, the complex viscosities (
η
∗) of the molten polymers were determined in experimental conditions of linear viscoelasticity.
T
g,
E
a and
η
∗ values increased linearly with PES% content, while
T
i and
T
1/2 values showed opposite behaviour. In every case both PES and PEES homopolymers felt outside linearity. The results obtained are discussed and interpreted, and compared with those of corresponding Cl-ended copolymers previously studied. |
doi_str_mv | 10.1016/j.polymdegradstab.2006.07.012 |
format | article |
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M
n
≅
9500
g
mol
−1), H
2N-ended polyethersulfone/polyetherethersulfone (PES/PEES) copolymers, at various PES/PEES ratios, were performed. The glass transition temperatures (
T
g) were determined by DSC. Degradations were carried out in a thermobalance, under flowing nitrogen, in dynamic heating conditions from 35
°C to 650
°C. The initial decomposition temperatures (
T
i) and the half decomposition temperatures (
T
1/2) were directly determined by TG curves, while the apparent activation energies of degradation (
E
a) were obtained by the Kissinger method. In addition, the complex viscosities (
η
∗) of the molten polymers were determined in experimental conditions of linear viscoelasticity.
T
g,
E
a and
η
∗ values increased linearly with PES% content, while
T
i and
T
1/2 values showed opposite behaviour. In every case both PES and PEES homopolymers felt outside linearity. The results obtained are discussed and interpreted, and compared with those of corresponding Cl-ended copolymers previously studied.</description><identifier>ISSN: 0141-3910</identifier><identifier>EISSN: 1873-2321</identifier><identifier>DOI: 10.1016/j.polymdegradstab.2006.07.012</identifier><identifier>CODEN: PDSTDW</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Applied sciences ; Chemical reactions and properties ; Copolymers ; Exact sciences and technology ; Gelation ; Kinetics of degradation ; Organic polymers ; Physicochemistry of polymers ; Properties and characterization ; Rheological behaviour ; Rheology and viscoelasticity ; Thermal stability</subject><ispartof>Polymer degradation and stability, 2006-12, Vol.91 (12), p.3230-3236</ispartof><rights>2006 Elsevier Ltd</rights><rights>2007 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c394t-22100fe2209ae4dbbcb4a3b4d40cf3df13f520488600dda6f8a773f2c25388303</citedby><cites>FETCH-LOGICAL-c394t-22100fe2209ae4dbbcb4a3b4d40cf3df13f520488600dda6f8a773f2c25388303</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=18336255$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Abate, Lorenzo</creatorcontrib><creatorcontrib>Blanco, Ignazio</creatorcontrib><creatorcontrib>Cicala, Gianluca</creatorcontrib><creatorcontrib>Recca, Antonino</creatorcontrib><creatorcontrib>Restuccia, Carmelo Luca</creatorcontrib><title>Thermal and rheological behaviours of some random aromatic amino-ended polyethersulfone/polyetherethersulfone copolymers</title><title>Polymer degradation and stability</title><description>The thermal and rheological characterizations of seven random, low molecular weight (
M
n
≅
9500
g
mol
−1), H
2N-ended polyethersulfone/polyetherethersulfone (PES/PEES) copolymers, at various PES/PEES ratios, were performed. The glass transition temperatures (
T
g) were determined by DSC. Degradations were carried out in a thermobalance, under flowing nitrogen, in dynamic heating conditions from 35
°C to 650
°C. The initial decomposition temperatures (
T
i) and the half decomposition temperatures (
T
1/2) were directly determined by TG curves, while the apparent activation energies of degradation (
E
a) were obtained by the Kissinger method. In addition, the complex viscosities (
η
∗) of the molten polymers were determined in experimental conditions of linear viscoelasticity.
T
g,
E
a and
η
∗ values increased linearly with PES% content, while
T
i and
T
1/2 values showed opposite behaviour. In every case both PES and PEES homopolymers felt outside linearity. The results obtained are discussed and interpreted, and compared with those of corresponding Cl-ended copolymers previously studied.</description><subject>Applied sciences</subject><subject>Chemical reactions and properties</subject><subject>Copolymers</subject><subject>Exact sciences and technology</subject><subject>Gelation</subject><subject>Kinetics of degradation</subject><subject>Organic polymers</subject><subject>Physicochemistry of polymers</subject><subject>Properties and characterization</subject><subject>Rheological behaviour</subject><subject>Rheology and viscoelasticity</subject><subject>Thermal stability</subject><issn>0141-3910</issn><issn>1873-2321</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNqNkD9v2zAQxYkiBeo4_Q5c0k3K8Y8keugQBK1bIECWZCYo8hjTkESXlI3425eOg7boFC4HPrx7d_cj5JpBzYC1N9t6F4fj6PA5GZdn09ccoK2hq4HxD2TBVCcqLji7IAtgklVixeATucx5C-XJhi3Iy-MG02gGaiZH0wbjEJ-DLf8eN-YQ4j5lGj3NcUSaiieO1KQ4mjlYasYwxQonh46eNsG5ZOX94OOEN3-Ef1Vq4-vKRbgiH70ZMn5-q0vy9P3b492P6v5h_fPu9r6yYiXninMG4JFzWBmUru9tL43opZNgvXCeCd9wkEq1AM6Z1ivTdcJzyxuhlACxJF_OubsUf-0xz3oM2eIwmAnjPmu-kqpTjSjGr2ejTTHnhF7vUhhNOmoG-sRbb_V_vPWJt4ZOF96l__ptkMkFoC-0bMh_Q5QQLW-a4luffViuPgRMOtuAk0UXEtpZuxjeOfE3q6ekOw</recordid><startdate>20061201</startdate><enddate>20061201</enddate><creator>Abate, Lorenzo</creator><creator>Blanco, Ignazio</creator><creator>Cicala, Gianluca</creator><creator>Recca, Antonino</creator><creator>Restuccia, Carmelo Luca</creator><general>Elsevier Ltd</general><general>Elsevier Science</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>20061201</creationdate><title>Thermal and rheological behaviours of some random aromatic amino-ended polyethersulfone/polyetherethersulfone copolymers</title><author>Abate, Lorenzo ; Blanco, Ignazio ; Cicala, Gianluca ; Recca, Antonino ; Restuccia, Carmelo Luca</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c394t-22100fe2209ae4dbbcb4a3b4d40cf3df13f520488600dda6f8a773f2c25388303</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Applied sciences</topic><topic>Chemical reactions and properties</topic><topic>Copolymers</topic><topic>Exact sciences and technology</topic><topic>Gelation</topic><topic>Kinetics of degradation</topic><topic>Organic polymers</topic><topic>Physicochemistry of polymers</topic><topic>Properties and characterization</topic><topic>Rheological behaviour</topic><topic>Rheology and viscoelasticity</topic><topic>Thermal stability</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Abate, Lorenzo</creatorcontrib><creatorcontrib>Blanco, Ignazio</creatorcontrib><creatorcontrib>Cicala, Gianluca</creatorcontrib><creatorcontrib>Recca, Antonino</creatorcontrib><creatorcontrib>Restuccia, Carmelo Luca</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Polymer degradation and stability</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Abate, Lorenzo</au><au>Blanco, Ignazio</au><au>Cicala, Gianluca</au><au>Recca, Antonino</au><au>Restuccia, Carmelo Luca</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Thermal and rheological behaviours of some random aromatic amino-ended polyethersulfone/polyetherethersulfone copolymers</atitle><jtitle>Polymer degradation and stability</jtitle><date>2006-12-01</date><risdate>2006</risdate><volume>91</volume><issue>12</issue><spage>3230</spage><epage>3236</epage><pages>3230-3236</pages><issn>0141-3910</issn><eissn>1873-2321</eissn><coden>PDSTDW</coden><abstract>The thermal and rheological characterizations of seven random, low molecular weight (
M
n
≅
9500
g
mol
−1), H
2N-ended polyethersulfone/polyetherethersulfone (PES/PEES) copolymers, at various PES/PEES ratios, were performed. The glass transition temperatures (
T
g) were determined by DSC. Degradations were carried out in a thermobalance, under flowing nitrogen, in dynamic heating conditions from 35
°C to 650
°C. The initial decomposition temperatures (
T
i) and the half decomposition temperatures (
T
1/2) were directly determined by TG curves, while the apparent activation energies of degradation (
E
a) were obtained by the Kissinger method. In addition, the complex viscosities (
η
∗) of the molten polymers were determined in experimental conditions of linear viscoelasticity.
T
g,
E
a and
η
∗ values increased linearly with PES% content, while
T
i and
T
1/2 values showed opposite behaviour. In every case both PES and PEES homopolymers felt outside linearity. The results obtained are discussed and interpreted, and compared with those of corresponding Cl-ended copolymers previously studied.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><doi>10.1016/j.polymdegradstab.2006.07.012</doi><tpages>7</tpages></addata></record> |
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language | eng |
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source | Elsevier |
subjects | Applied sciences Chemical reactions and properties Copolymers Exact sciences and technology Gelation Kinetics of degradation Organic polymers Physicochemistry of polymers Properties and characterization Rheological behaviour Rheology and viscoelasticity Thermal stability |
title | Thermal and rheological behaviours of some random aromatic amino-ended polyethersulfone/polyetherethersulfone copolymers |
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