Loading…

Tough interpenetrating Pluronic F127/polyacrylic acid hydrogels

Tough interpenetrating polymer network (IPN) hydrogels with pH- and temperature sensitivity were prepared by crosslinking copolymerization of acrylic acid (AAc) and N,N′-methylenebis(acrylamide) in 20 w/v% aqueous solutions of F127 (PEO99-PPO65-PEO99). The presence of F127 within the gel network sli...

Full description

Saved in:
Bibliographic Details
Published in:Polymer (Guilford) 2013-05, Vol.54 (12), p.2979-2987
Main Authors: Baskan, Tuba, Tuncaboylu, Deniz C., Okay, Oguz
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-c396t-bfaed3a8af54f30487c67ef6f92bfefabbf3d6a994da6a3200b5f3c07ae7eb313
cites cdi_FETCH-LOGICAL-c396t-bfaed3a8af54f30487c67ef6f92bfefabbf3d6a994da6a3200b5f3c07ae7eb313
container_end_page 2987
container_issue 12
container_start_page 2979
container_title Polymer (Guilford)
container_volume 54
creator Baskan, Tuba
Tuncaboylu, Deniz C.
Okay, Oguz
description Tough interpenetrating polymer network (IPN) hydrogels with pH- and temperature sensitivity were prepared by crosslinking copolymerization of acrylic acid (AAc) and N,N′-methylenebis(acrylamide) in 20 w/v% aqueous solutions of F127 (PEO99-PPO65-PEO99). The presence of F127 within the gel network slightly decreases the elastic modulus while the loss factor significantly increases, revealing increasing energy dissipation in IPN hydrogels. Cyclic compression tests show large mechanical hysteresis in IPN hydrogels due to the reversible formation of ionic clusters and hydrophobic associations of F127 molecules. The dissipative mechanisms created by F127 lead to the improvement in the mechanical performance of IPN hydrogels when compared to the polyacrylic acid (PAAc) gel controls. PAAc hydrogel formed at 10% AAc fractures under a compression of 0.2 MPa at 78% strain, while the corresponding IPN hydrogel sustains up to 7 MPa compressions at 98% strain, leading to an increase of toughness from 31 to 335 kJ/m3. IPN hydrogels subjected to the heating–cooling cycles between below and above the micellization temperature of F127 show characteristic features of F127 solutions, i.e., increase of the dynamic moduli on raising the temperature, and thermal hysteresis behavior. [Display omitted]
doi_str_mv 10.1016/j.polymer.2013.03.066
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1677900854</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0032386113003005</els_id><sourcerecordid>1677900854</sourcerecordid><originalsourceid>FETCH-LOGICAL-c396t-bfaed3a8af54f30487c67ef6f92bfefabbf3d6a994da6a3200b5f3c07ae7eb313</originalsourceid><addsrcrecordid>eNqFkEFrGzEQhUVJIY7bnxDqS6GXtUfSrrR7CsU0TcCQQJOzmNWOHJn1ypXWAf_7arHpNTAwMHzvveExdsthyYGr1W55CP1pT3EpgMsl5FHqE5vxWstCiIZfsRmAFIWsFb9mNyntAEBUopyxu5dw3L4t_DBSPNBAY8TRD9vFc3-MYfB2cc-FXk3-aOOpzwe0vlu8nboYttSnL-yzwz7R18ues9f7Xy_rh2Lz9Ptx_XNTWNmosWgdUiexRleVTkJZa6s0OeUa0Tpy2LZOdgqbpuxQoRQAbeWkBY2kqZVcztmPs-8hhr9HSqPZ-2Sp73GgcEyGK60bgLoqM1qdURtDSpGcOUS_x3gyHMxUmNmZS2FmKsxAHqWy7vslApPF3kUcrE__xULLphZ64r6dOYfB4DZm5vVPNqoAOEBVTsTdmcgF0bvPOcl6Gix1PpIdTRf8B7_8A0xYjoE</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1677900854</pqid></control><display><type>article</type><title>Tough interpenetrating Pluronic F127/polyacrylic acid hydrogels</title><source>Elsevier:Jisc Collections:Elsevier Read and Publish Agreement 2022-2024:Freedom Collection (Reading list)</source><creator>Baskan, Tuba ; Tuncaboylu, Deniz C. ; Okay, Oguz</creator><creatorcontrib>Baskan, Tuba ; Tuncaboylu, Deniz C. ; Okay, Oguz</creatorcontrib><description>Tough interpenetrating polymer network (IPN) hydrogels with pH- and temperature sensitivity were prepared by crosslinking copolymerization of acrylic acid (AAc) and N,N′-methylenebis(acrylamide) in 20 w/v% aqueous solutions of F127 (PEO99-PPO65-PEO99). The presence of F127 within the gel network slightly decreases the elastic modulus while the loss factor significantly increases, revealing increasing energy dissipation in IPN hydrogels. Cyclic compression tests show large mechanical hysteresis in IPN hydrogels due to the reversible formation of ionic clusters and hydrophobic associations of F127 molecules. The dissipative mechanisms created by F127 lead to the improvement in the mechanical performance of IPN hydrogels when compared to the polyacrylic acid (PAAc) gel controls. PAAc hydrogel formed at 10% AAc fractures under a compression of 0.2 MPa at 78% strain, while the corresponding IPN hydrogel sustains up to 7 MPa compressions at 98% strain, leading to an increase of toughness from 31 to 335 kJ/m3. IPN hydrogels subjected to the heating–cooling cycles between below and above the micellization temperature of F127 show characteristic features of F127 solutions, i.e., increase of the dynamic moduli on raising the temperature, and thermal hysteresis behavior. [Display omitted]</description><identifier>ISSN: 0032-3861</identifier><identifier>EISSN: 1873-2291</identifier><identifier>DOI: 10.1016/j.polymer.2013.03.066</identifier><identifier>CODEN: POLMAG</identifier><language>eng</language><publisher>Kidlington: Elsevier Ltd</publisher><subject>acrylamides ; acrylic acid ; Applied sciences ; aqueous solutions ; Compressing ; Crosslinking ; Elastic modulus ; energy ; Exact sciences and technology ; gels ; hydrocolloids ; Hydrogels ; Hydrophobic associations ; hydrophobicity ; Hysteresis ; modulus of elasticity ; Networks ; Organic polymers ; Physicochemistry of polymers ; Pluronic F127 ; Polyacrylic acid ; Properties and characterization ; Solution and gel properties ; Strain ; temperature ; Toughness</subject><ispartof>Polymer (Guilford), 2013-05, Vol.54 (12), p.2979-2987</ispartof><rights>2013 Elsevier Ltd</rights><rights>2014 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c396t-bfaed3a8af54f30487c67ef6f92bfefabbf3d6a994da6a3200b5f3c07ae7eb313</citedby><cites>FETCH-LOGICAL-c396t-bfaed3a8af54f30487c67ef6f92bfefabbf3d6a994da6a3200b5f3c07ae7eb313</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=27398276$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Baskan, Tuba</creatorcontrib><creatorcontrib>Tuncaboylu, Deniz C.</creatorcontrib><creatorcontrib>Okay, Oguz</creatorcontrib><title>Tough interpenetrating Pluronic F127/polyacrylic acid hydrogels</title><title>Polymer (Guilford)</title><description>Tough interpenetrating polymer network (IPN) hydrogels with pH- and temperature sensitivity were prepared by crosslinking copolymerization of acrylic acid (AAc) and N,N′-methylenebis(acrylamide) in 20 w/v% aqueous solutions of F127 (PEO99-PPO65-PEO99). The presence of F127 within the gel network slightly decreases the elastic modulus while the loss factor significantly increases, revealing increasing energy dissipation in IPN hydrogels. Cyclic compression tests show large mechanical hysteresis in IPN hydrogels due to the reversible formation of ionic clusters and hydrophobic associations of F127 molecules. The dissipative mechanisms created by F127 lead to the improvement in the mechanical performance of IPN hydrogels when compared to the polyacrylic acid (PAAc) gel controls. PAAc hydrogel formed at 10% AAc fractures under a compression of 0.2 MPa at 78% strain, while the corresponding IPN hydrogel sustains up to 7 MPa compressions at 98% strain, leading to an increase of toughness from 31 to 335 kJ/m3. IPN hydrogels subjected to the heating–cooling cycles between below and above the micellization temperature of F127 show characteristic features of F127 solutions, i.e., increase of the dynamic moduli on raising the temperature, and thermal hysteresis behavior. [Display omitted]</description><subject>acrylamides</subject><subject>acrylic acid</subject><subject>Applied sciences</subject><subject>aqueous solutions</subject><subject>Compressing</subject><subject>Crosslinking</subject><subject>Elastic modulus</subject><subject>energy</subject><subject>Exact sciences and technology</subject><subject>gels</subject><subject>hydrocolloids</subject><subject>Hydrogels</subject><subject>Hydrophobic associations</subject><subject>hydrophobicity</subject><subject>Hysteresis</subject><subject>modulus of elasticity</subject><subject>Networks</subject><subject>Organic polymers</subject><subject>Physicochemistry of polymers</subject><subject>Pluronic F127</subject><subject>Polyacrylic acid</subject><subject>Properties and characterization</subject><subject>Solution and gel properties</subject><subject>Strain</subject><subject>temperature</subject><subject>Toughness</subject><issn>0032-3861</issn><issn>1873-2291</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNqFkEFrGzEQhUVJIY7bnxDqS6GXtUfSrrR7CsU0TcCQQJOzmNWOHJn1ypXWAf_7arHpNTAwMHzvveExdsthyYGr1W55CP1pT3EpgMsl5FHqE5vxWstCiIZfsRmAFIWsFb9mNyntAEBUopyxu5dw3L4t_DBSPNBAY8TRD9vFc3-MYfB2cc-FXk3-aOOpzwe0vlu8nboYttSnL-yzwz7R18ues9f7Xy_rh2Lz9Ptx_XNTWNmosWgdUiexRleVTkJZa6s0OeUa0Tpy2LZOdgqbpuxQoRQAbeWkBY2kqZVcztmPs-8hhr9HSqPZ-2Sp73GgcEyGK60bgLoqM1qdURtDSpGcOUS_x3gyHMxUmNmZS2FmKsxAHqWy7vslApPF3kUcrE__xULLphZ64r6dOYfB4DZm5vVPNqoAOEBVTsTdmcgF0bvPOcl6Gix1PpIdTRf8B7_8A0xYjoE</recordid><startdate>20130501</startdate><enddate>20130501</enddate><creator>Baskan, Tuba</creator><creator>Tuncaboylu, Deniz C.</creator><creator>Okay, Oguz</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>FBQ</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8FD</scope><scope>F28</scope><scope>FR3</scope><scope>JG9</scope><scope>L7M</scope></search><sort><creationdate>20130501</creationdate><title>Tough interpenetrating Pluronic F127/polyacrylic acid hydrogels</title><author>Baskan, Tuba ; Tuncaboylu, Deniz C. ; Okay, Oguz</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c396t-bfaed3a8af54f30487c67ef6f92bfefabbf3d6a994da6a3200b5f3c07ae7eb313</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>acrylamides</topic><topic>acrylic acid</topic><topic>Applied sciences</topic><topic>aqueous solutions</topic><topic>Compressing</topic><topic>Crosslinking</topic><topic>Elastic modulus</topic><topic>energy</topic><topic>Exact sciences and technology</topic><topic>gels</topic><topic>hydrocolloids</topic><topic>Hydrogels</topic><topic>Hydrophobic associations</topic><topic>hydrophobicity</topic><topic>Hysteresis</topic><topic>modulus of elasticity</topic><topic>Networks</topic><topic>Organic polymers</topic><topic>Physicochemistry of polymers</topic><topic>Pluronic F127</topic><topic>Polyacrylic acid</topic><topic>Properties and characterization</topic><topic>Solution and gel properties</topic><topic>Strain</topic><topic>temperature</topic><topic>Toughness</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Baskan, Tuba</creatorcontrib><creatorcontrib>Tuncaboylu, Deniz C.</creatorcontrib><creatorcontrib>Okay, Oguz</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>ANTE: Abstracts in New Technology &amp; Engineering</collection><collection>Engineering Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Polymer (Guilford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Baskan, Tuba</au><au>Tuncaboylu, Deniz C.</au><au>Okay, Oguz</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tough interpenetrating Pluronic F127/polyacrylic acid hydrogels</atitle><jtitle>Polymer (Guilford)</jtitle><date>2013-05-01</date><risdate>2013</risdate><volume>54</volume><issue>12</issue><spage>2979</spage><epage>2987</epage><pages>2979-2987</pages><issn>0032-3861</issn><eissn>1873-2291</eissn><coden>POLMAG</coden><abstract>Tough interpenetrating polymer network (IPN) hydrogels with pH- and temperature sensitivity were prepared by crosslinking copolymerization of acrylic acid (AAc) and N,N′-methylenebis(acrylamide) in 20 w/v% aqueous solutions of F127 (PEO99-PPO65-PEO99). The presence of F127 within the gel network slightly decreases the elastic modulus while the loss factor significantly increases, revealing increasing energy dissipation in IPN hydrogels. Cyclic compression tests show large mechanical hysteresis in IPN hydrogels due to the reversible formation of ionic clusters and hydrophobic associations of F127 molecules. The dissipative mechanisms created by F127 lead to the improvement in the mechanical performance of IPN hydrogels when compared to the polyacrylic acid (PAAc) gel controls. PAAc hydrogel formed at 10% AAc fractures under a compression of 0.2 MPa at 78% strain, while the corresponding IPN hydrogel sustains up to 7 MPa compressions at 98% strain, leading to an increase of toughness from 31 to 335 kJ/m3. IPN hydrogels subjected to the heating–cooling cycles between below and above the micellization temperature of F127 show characteristic features of F127 solutions, i.e., increase of the dynamic moduli on raising the temperature, and thermal hysteresis behavior. [Display omitted]</abstract><cop>Kidlington</cop><pub>Elsevier Ltd</pub><doi>10.1016/j.polymer.2013.03.066</doi><tpages>9</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0032-3861
ispartof Polymer (Guilford), 2013-05, Vol.54 (12), p.2979-2987
issn 0032-3861
1873-2291
language eng
recordid cdi_proquest_miscellaneous_1677900854
source Elsevier:Jisc Collections:Elsevier Read and Publish Agreement 2022-2024:Freedom Collection (Reading list)
subjects acrylamides
acrylic acid
Applied sciences
aqueous solutions
Compressing
Crosslinking
Elastic modulus
energy
Exact sciences and technology
gels
hydrocolloids
Hydrogels
Hydrophobic associations
hydrophobicity
Hysteresis
modulus of elasticity
Networks
Organic polymers
Physicochemistry of polymers
Pluronic F127
Polyacrylic acid
Properties and characterization
Solution and gel properties
Strain
temperature
Toughness
title Tough interpenetrating Pluronic F127/polyacrylic acid hydrogels
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-01T04%3A51%3A11IST&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=Tough%20interpenetrating%20Pluronic%20F127/polyacrylic%20acid%20hydrogels&rft.jtitle=Polymer%20(Guilford)&rft.au=Baskan,%20Tuba&rft.date=2013-05-01&rft.volume=54&rft.issue=12&rft.spage=2979&rft.epage=2987&rft.pages=2979-2987&rft.issn=0032-3861&rft.eissn=1873-2291&rft.coden=POLMAG&rft_id=info:doi/10.1016/j.polymer.2013.03.066&rft_dat=%3Cproquest_cross%3E1677900854%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c396t-bfaed3a8af54f30487c67ef6f92bfefabbf3d6a994da6a3200b5f3c07ae7eb313%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1677900854&rft_id=info:pmid/&rfr_iscdi=true