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Synthesis and Properties of SEPS-g-PEO Copolymers with Varying Branch Lengths
Poly(ethylene oxide) (PEO) was controllably grafted from styrene- b -(ethylene- co -propylene)- b -styrene (SEPS) backbones by combining lithiation of styrenic units and living monomer-activated anionic ring-opening polymerization of ethylene oxide (EO) monomers with the aid of co-initiators triisob...
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Published in: | Chinese journal of polymer science 2018-08, Vol.36 (8), p.934-942 |
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container_title | Chinese journal of polymer science |
container_volume | 36 |
creator | Zhao, Zhong-Fu Liu, Pei-Ying Zhang, Chun-Qing Liu, Wei Wang, Yan-Hui Tang, Tao Ding, Yi-Fu Zhang, Yan-Dong Meng, Fan-Zhi |
description | Poly(ethylene oxide) (PEO) was controllably grafted from styrene-
b
-(ethylene-
co
-propylene)-
b
-styrene (SEPS) backbones by combining lithiation of styrenic units and living monomer-activated anionic ring-opening polymerization of ethylene oxide (EO) monomers with the aid of co-initiators triisobutyl aluminum. The as-synthesized SEPS-
g
-PEO copolymers were characterized by SEC,
1
H-NMR, FTIR, SAXS, AFM and DSC. When the branch length is relatively small, increase of PEO fraction leads to the increase of the correlation length between neighboring hard domains, but the degree of correlation reduces. When the branch length is relatively large, the phase-separated structures become random both in terms of size and spatial correlation, and macro-phase separated structures appear. The crystallization behavior of the PEO branches can be effectively inhibited in SEPS-
g
-PEO, so no significant crystallization takes place until the fraction of PEO branches is 20.1 wt%, which greatly promotes the rapid delivery of hydrophilic drugs in the hot-melting pressuresensitive adhesives (HMPSAs) based on SEPS-
g
-PEO. Their cumulative release amount of a model drug could achieve 80%, more than twice the value in the HMPSAs based on linear PEO-containing styrenic block copolymers. |
doi_str_mv | 10.1007/s10118-018-2104-0 |
format | article |
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b
-(ethylene-
co
-propylene)-
b
-styrene (SEPS) backbones by combining lithiation of styrenic units and living monomer-activated anionic ring-opening polymerization of ethylene oxide (EO) monomers with the aid of co-initiators triisobutyl aluminum. The as-synthesized SEPS-
g
-PEO copolymers were characterized by SEC,
1
H-NMR, FTIR, SAXS, AFM and DSC. When the branch length is relatively small, increase of PEO fraction leads to the increase of the correlation length between neighboring hard domains, but the degree of correlation reduces. When the branch length is relatively large, the phase-separated structures become random both in terms of size and spatial correlation, and macro-phase separated structures appear. The crystallization behavior of the PEO branches can be effectively inhibited in SEPS-
g
-PEO, so no significant crystallization takes place until the fraction of PEO branches is 20.1 wt%, which greatly promotes the rapid delivery of hydrophilic drugs in the hot-melting pressuresensitive adhesives (HMPSAs) based on SEPS-
g
-PEO. Their cumulative release amount of a model drug could achieve 80%, more than twice the value in the HMPSAs based on linear PEO-containing styrenic block copolymers.</description><identifier>ISSN: 0256-7679</identifier><identifier>EISSN: 1439-6203</identifier><identifier>DOI: 10.1007/s10118-018-2104-0</identifier><language>eng</language><publisher>Beijing: Chinese Chemical Society and Institute of Chemistry, CAS</publisher><subject>Aluminum ; Block copolymers ; Characterization and Evaluation of Materials ; Chemical industry ; Chemical synthesis ; Chemistry ; Chemistry and Materials Science ; Condensed Matter Physics ; Correlation ; Crystallization ; Drug delivery systems ; Ethylene oxide ; Industrial Chemistry/Chemical Engineering ; Initiators ; Monomers ; NMR ; Nuclear magnetic resonance ; Polymer Sciences ; Propylene ; Ring opening polymerization ; Styrenes</subject><ispartof>Chinese journal of polymer science, 2018-08, Vol.36 (8), p.934-942</ispartof><rights>Chinese Chemical Society, Institute of Chemistry, Chinese Academy of Sciences and Springer-Verlag GmbH Germany, part of Springer Nature 2018</rights><rights>Copyright Springer Science & Business Media 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c316t-ed9185a7867bd8137e44f7ef96fea37cf5a681d0afd23ef46ef86b9be6e99e063</citedby><cites>FETCH-LOGICAL-c316t-ed9185a7867bd8137e44f7ef96fea37cf5a681d0afd23ef46ef86b9be6e99e063</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></links><search><creatorcontrib>Zhao, Zhong-Fu</creatorcontrib><creatorcontrib>Liu, Pei-Ying</creatorcontrib><creatorcontrib>Zhang, Chun-Qing</creatorcontrib><creatorcontrib>Liu, Wei</creatorcontrib><creatorcontrib>Wang, Yan-Hui</creatorcontrib><creatorcontrib>Tang, Tao</creatorcontrib><creatorcontrib>Ding, Yi-Fu</creatorcontrib><creatorcontrib>Zhang, Yan-Dong</creatorcontrib><creatorcontrib>Meng, Fan-Zhi</creatorcontrib><title>Synthesis and Properties of SEPS-g-PEO Copolymers with Varying Branch Lengths</title><title>Chinese journal of polymer science</title><addtitle>Chin J Polym Sci</addtitle><description>Poly(ethylene oxide) (PEO) was controllably grafted from styrene-
b
-(ethylene-
co
-propylene)-
b
-styrene (SEPS) backbones by combining lithiation of styrenic units and living monomer-activated anionic ring-opening polymerization of ethylene oxide (EO) monomers with the aid of co-initiators triisobutyl aluminum. The as-synthesized SEPS-
g
-PEO copolymers were characterized by SEC,
1
H-NMR, FTIR, SAXS, AFM and DSC. When the branch length is relatively small, increase of PEO fraction leads to the increase of the correlation length between neighboring hard domains, but the degree of correlation reduces. When the branch length is relatively large, the phase-separated structures become random both in terms of size and spatial correlation, and macro-phase separated structures appear. The crystallization behavior of the PEO branches can be effectively inhibited in SEPS-
g
-PEO, so no significant crystallization takes place until the fraction of PEO branches is 20.1 wt%, which greatly promotes the rapid delivery of hydrophilic drugs in the hot-melting pressuresensitive adhesives (HMPSAs) based on SEPS-
g
-PEO. Their cumulative release amount of a model drug could achieve 80%, more than twice the value in the HMPSAs based on linear PEO-containing styrenic block copolymers.</description><subject>Aluminum</subject><subject>Block copolymers</subject><subject>Characterization and Evaluation of Materials</subject><subject>Chemical industry</subject><subject>Chemical synthesis</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Condensed Matter Physics</subject><subject>Correlation</subject><subject>Crystallization</subject><subject>Drug delivery systems</subject><subject>Ethylene oxide</subject><subject>Industrial Chemistry/Chemical Engineering</subject><subject>Initiators</subject><subject>Monomers</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Polymer Sciences</subject><subject>Propylene</subject><subject>Ring opening polymerization</subject><subject>Styrenes</subject><issn>0256-7679</issn><issn>1439-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp1kF1LwzAUhoMoOKc_wLuA19GTJk2aSx3zAyYbTL0NWXvSdmxtTSqyf29HBa-8OJyb93nP4SHkmsMtB9B3kQPnGYNhEg6SwQmZcCkMUwmIUzKBJFVMK23OyUWMWwAldaon5HV9aPoKYx2pawq6Cm2Hoa8x0tbT9Xy1ZiVbzZd01nbt7rDHEOl33Vf0w4VD3ZT0Ibgmr-gCm7Kv4iU5824X8ep3T8n74_xt9swWy6eX2f2C5YKrnmFheJY6nSm9KTIuNErpNXqjPDqhc586lfECnC8SgV4q9JnamA0qNAZBiSm5GXu70H5-Yezttv0KzXDSJqDASA4ZDCk-pvLQxhjQ2y7U--Fxy8EerdnRmh2s2aM1e2SSkYlDtikx_DX_D_0A1ZVvBQ</recordid><startdate>20180801</startdate><enddate>20180801</enddate><creator>Zhao, Zhong-Fu</creator><creator>Liu, Pei-Ying</creator><creator>Zhang, Chun-Qing</creator><creator>Liu, Wei</creator><creator>Wang, Yan-Hui</creator><creator>Tang, Tao</creator><creator>Ding, Yi-Fu</creator><creator>Zhang, Yan-Dong</creator><creator>Meng, Fan-Zhi</creator><general>Chinese Chemical Society and Institute of Chemistry, CAS</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20180801</creationdate><title>Synthesis and Properties of SEPS-g-PEO Copolymers with Varying Branch Lengths</title><author>Zhao, Zhong-Fu ; Liu, Pei-Ying ; Zhang, Chun-Qing ; Liu, Wei ; Wang, Yan-Hui ; Tang, Tao ; Ding, Yi-Fu ; Zhang, Yan-Dong ; Meng, Fan-Zhi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c316t-ed9185a7867bd8137e44f7ef96fea37cf5a681d0afd23ef46ef86b9be6e99e063</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Aluminum</topic><topic>Block copolymers</topic><topic>Characterization and Evaluation of Materials</topic><topic>Chemical industry</topic><topic>Chemical synthesis</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Condensed Matter Physics</topic><topic>Correlation</topic><topic>Crystallization</topic><topic>Drug delivery systems</topic><topic>Ethylene oxide</topic><topic>Industrial Chemistry/Chemical Engineering</topic><topic>Initiators</topic><topic>Monomers</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><topic>Polymer Sciences</topic><topic>Propylene</topic><topic>Ring opening polymerization</topic><topic>Styrenes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhao, Zhong-Fu</creatorcontrib><creatorcontrib>Liu, Pei-Ying</creatorcontrib><creatorcontrib>Zhang, Chun-Qing</creatorcontrib><creatorcontrib>Liu, Wei</creatorcontrib><creatorcontrib>Wang, Yan-Hui</creatorcontrib><creatorcontrib>Tang, Tao</creatorcontrib><creatorcontrib>Ding, Yi-Fu</creatorcontrib><creatorcontrib>Zhang, Yan-Dong</creatorcontrib><creatorcontrib>Meng, Fan-Zhi</creatorcontrib><collection>CrossRef</collection><jtitle>Chinese journal of polymer science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhao, Zhong-Fu</au><au>Liu, Pei-Ying</au><au>Zhang, Chun-Qing</au><au>Liu, Wei</au><au>Wang, Yan-Hui</au><au>Tang, Tao</au><au>Ding, Yi-Fu</au><au>Zhang, Yan-Dong</au><au>Meng, Fan-Zhi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis and Properties of SEPS-g-PEO Copolymers with Varying Branch Lengths</atitle><jtitle>Chinese journal of polymer science</jtitle><stitle>Chin J Polym Sci</stitle><date>2018-08-01</date><risdate>2018</risdate><volume>36</volume><issue>8</issue><spage>934</spage><epage>942</epage><pages>934-942</pages><issn>0256-7679</issn><eissn>1439-6203</eissn><abstract>Poly(ethylene oxide) (PEO) was controllably grafted from styrene-
b
-(ethylene-
co
-propylene)-
b
-styrene (SEPS) backbones by combining lithiation of styrenic units and living monomer-activated anionic ring-opening polymerization of ethylene oxide (EO) monomers with the aid of co-initiators triisobutyl aluminum. The as-synthesized SEPS-
g
-PEO copolymers were characterized by SEC,
1
H-NMR, FTIR, SAXS, AFM and DSC. When the branch length is relatively small, increase of PEO fraction leads to the increase of the correlation length between neighboring hard domains, but the degree of correlation reduces. When the branch length is relatively large, the phase-separated structures become random both in terms of size and spatial correlation, and macro-phase separated structures appear. The crystallization behavior of the PEO branches can be effectively inhibited in SEPS-
g
-PEO, so no significant crystallization takes place until the fraction of PEO branches is 20.1 wt%, which greatly promotes the rapid delivery of hydrophilic drugs in the hot-melting pressuresensitive adhesives (HMPSAs) based on SEPS-
g
-PEO. Their cumulative release amount of a model drug could achieve 80%, more than twice the value in the HMPSAs based on linear PEO-containing styrenic block copolymers.</abstract><cop>Beijing</cop><pub>Chinese Chemical Society and Institute of Chemistry, CAS</pub><doi>10.1007/s10118-018-2104-0</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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language | eng |
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source | Springer Nature |
subjects | Aluminum Block copolymers Characterization and Evaluation of Materials Chemical industry Chemical synthesis Chemistry Chemistry and Materials Science Condensed Matter Physics Correlation Crystallization Drug delivery systems Ethylene oxide Industrial Chemistry/Chemical Engineering Initiators Monomers NMR Nuclear magnetic resonance Polymer Sciences Propylene Ring opening polymerization Styrenes |
title | Synthesis and Properties of SEPS-g-PEO Copolymers with Varying Branch Lengths |
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