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Glycerol-modified poly(ε-caprolactone): an biocatalytic approach to improve the hydrophilicity of poly(ε-caprolactone)
Novel poly(ε-caprolactone) (PCL)–glycerol polyester was synthesized in one step in the presence of Novozym 435 under mild reaction conditions. The objective of the study was to investigate the feasibility of enhancing the hydrophilicity of PCL by condensing it with glycerol through biocatalytic appr...
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Published in: | Polymer bulletin (Berlin, Germany) Germany), 2019-04, Vol.76 (4), p.1915-1928 |
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container_end_page | 1928 |
container_issue | 4 |
container_start_page | 1915 |
container_title | Polymer bulletin (Berlin, Germany) |
container_volume | 76 |
creator | Chakraborty, Soma Pagaduan, James Nicolas M. Melgar, Zara Kryzel A. Seitz, Steffen Kan, Kai Ajiro, Hiroharu |
description | Novel poly(ε-caprolactone) (PCL)–glycerol polyester was synthesized in one step in the presence of Novozym 435 under mild reaction conditions. The objective of the study was to investigate the feasibility of enhancing the hydrophilicity of PCL by condensing it with glycerol through biocatalytic approach. Effect of reaction time, glycerol-to-CL ratio and CL-to-toluene ratio was studied. The
1
H NMR and GPC results established that self-condensation of CL units and condensation of CL with glycerol units take place simultaneously. When the glycerol content was 10 and 20 mol% with regard to CL, condensation continued for 6 h; further extension of reaction time resulted in the cleavage of ester linkages. When the glycerol content was increased to 40 mol%, the condensation of CL–glycerol units was accomplished in 4 h; however, the reaction had to get extended beyond 6 h for complete condensation of CL–CL units. The study revealed that the crystallinity and the melting temperature (
T
m
) of the products altered with an increase in the glycerol content. Furthermore, TGA and contact angle values of water on PCL and its glycerol derivative films revealed that the water uptake capacity of PCL too increased significantly with the increase in glycerol content, rendering PCL more hydrophilic. |
doi_str_mv | 10.1007/s00289-018-2443-6 |
format | article |
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1
H NMR and GPC results established that self-condensation of CL units and condensation of CL with glycerol units take place simultaneously. When the glycerol content was 10 and 20 mol% with regard to CL, condensation continued for 6 h; further extension of reaction time resulted in the cleavage of ester linkages. When the glycerol content was increased to 40 mol%, the condensation of CL–glycerol units was accomplished in 4 h; however, the reaction had to get extended beyond 6 h for complete condensation of CL–CL units. The study revealed that the crystallinity and the melting temperature (
T
m
) of the products altered with an increase in the glycerol content. Furthermore, TGA and contact angle values of water on PCL and its glycerol derivative films revealed that the water uptake capacity of PCL too increased significantly with the increase in glycerol content, rendering PCL more hydrophilic.</description><identifier>ISSN: 0170-0839</identifier><identifier>EISSN: 1436-2449</identifier><identifier>DOI: 10.1007/s00289-018-2443-6</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Characterization and Evaluation of Materials ; Chemistry ; Chemistry and Materials Science ; Complex Fluids and Microfluidics ; Condensates ; Contact angle ; Glycerol ; Hydrophilicity ; Melt temperature ; Molecular weight ; NMR ; Nuclear magnetic resonance ; Organic Chemistry ; Original Paper ; Physical Chemistry ; Polycaprolactone ; Polymer Sciences ; Polymerization ; Polymers ; Reaction time ; Soft and Granular Matter ; Software ; Tissue engineering ; Toluene</subject><ispartof>Polymer bulletin (Berlin, Germany), 2019-04, Vol.76 (4), p.1915-1928</ispartof><rights>Springer-Verlag GmbH Germany, part of Springer Nature 2018</rights><rights>Springer-Verlag GmbH Germany, part of Springer Nature 2018.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c316t-c2387cf2ded81b29e1f4e0412a90cf1f3a06983afc24f04156539269632f73613</citedby><cites>FETCH-LOGICAL-c316t-c2387cf2ded81b29e1f4e0412a90cf1f3a06983afc24f04156539269632f73613</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>Chakraborty, Soma</creatorcontrib><creatorcontrib>Pagaduan, James Nicolas M.</creatorcontrib><creatorcontrib>Melgar, Zara Kryzel A.</creatorcontrib><creatorcontrib>Seitz, Steffen</creatorcontrib><creatorcontrib>Kan, Kai</creatorcontrib><creatorcontrib>Ajiro, Hiroharu</creatorcontrib><title>Glycerol-modified poly(ε-caprolactone): an biocatalytic approach to improve the hydrophilicity of poly(ε-caprolactone)</title><title>Polymer bulletin (Berlin, Germany)</title><addtitle>Polym. Bull</addtitle><description>Novel poly(ε-caprolactone) (PCL)–glycerol polyester was synthesized in one step in the presence of Novozym 435 under mild reaction conditions. The objective of the study was to investigate the feasibility of enhancing the hydrophilicity of PCL by condensing it with glycerol through biocatalytic approach. Effect of reaction time, glycerol-to-CL ratio and CL-to-toluene ratio was studied. The
1
H NMR and GPC results established that self-condensation of CL units and condensation of CL with glycerol units take place simultaneously. When the glycerol content was 10 and 20 mol% with regard to CL, condensation continued for 6 h; further extension of reaction time resulted in the cleavage of ester linkages. When the glycerol content was increased to 40 mol%, the condensation of CL–glycerol units was accomplished in 4 h; however, the reaction had to get extended beyond 6 h for complete condensation of CL–CL units. The study revealed that the crystallinity and the melting temperature (
T
m
) of the products altered with an increase in the glycerol content. Furthermore, TGA and contact angle values of water on PCL and its glycerol derivative films revealed that the water uptake capacity of PCL too increased significantly with the increase in glycerol content, rendering PCL more hydrophilic.</description><subject>Characterization and Evaluation of Materials</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Complex Fluids and Microfluidics</subject><subject>Condensates</subject><subject>Contact angle</subject><subject>Glycerol</subject><subject>Hydrophilicity</subject><subject>Melt temperature</subject><subject>Molecular weight</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Organic Chemistry</subject><subject>Original Paper</subject><subject>Physical Chemistry</subject><subject>Polycaprolactone</subject><subject>Polymer Sciences</subject><subject>Polymerization</subject><subject>Polymers</subject><subject>Reaction time</subject><subject>Soft and Granular Matter</subject><subject>Software</subject><subject>Tissue engineering</subject><subject>Toluene</subject><issn>0170-0839</issn><issn>1436-2449</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp1UMtKAzEUDaJgrX6Au4AbXUTzmGYSd1K0CoIbXYc0kzgp02ZMUnE-zN_wm0wZwY2u7r3nngccAE4JviQY11cJYyokwkQgWlUM8T0wIRXju0vugwkmNUZYMHkIjlJa4XJzTibgY9ENxsbQoXVovPO2gX3ohvOvT2R0X3BtctjYi2uoN3Dpg9FZd0P2Buq-vLVpYQ7Qr8v-bmFuLWyHJoa-9Z03Pg8wuL8Nj8GB012yJz9zCl7ubp_n9-jxafEwv3lEhhGekaFM1MbRxjaCLKm0xFUWV4RqiY0jjmnMpWDaGVq5gs_4jEnKJWfU1YwTNgVno2_JftvalNUqbOOmRCoqSS1qVhNRWGRkmRhSitapPvq1joMiWO0KVmPBqhSsdgUrXjR01KTC3bza-Ov8v-gb_MuAfg</recordid><startdate>20190401</startdate><enddate>20190401</enddate><creator>Chakraborty, Soma</creator><creator>Pagaduan, James Nicolas M.</creator><creator>Melgar, Zara Kryzel A.</creator><creator>Seitz, Steffen</creator><creator>Kan, Kai</creator><creator>Ajiro, Hiroharu</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>8FE</scope><scope>8FG</scope><scope>ABJCF</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>HCIFZ</scope><scope>KB.</scope><scope>PDBOC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope></search><sort><creationdate>20190401</creationdate><title>Glycerol-modified poly(ε-caprolactone): an biocatalytic approach to improve the hydrophilicity of poly(ε-caprolactone)</title><author>Chakraborty, Soma ; Pagaduan, James Nicolas M. ; Melgar, Zara Kryzel A. ; Seitz, Steffen ; Kan, Kai ; Ajiro, Hiroharu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c316t-c2387cf2ded81b29e1f4e0412a90cf1f3a06983afc24f04156539269632f73613</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Characterization and Evaluation of Materials</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Complex Fluids and Microfluidics</topic><topic>Condensates</topic><topic>Contact angle</topic><topic>Glycerol</topic><topic>Hydrophilicity</topic><topic>Melt temperature</topic><topic>Molecular weight</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><topic>Organic Chemistry</topic><topic>Original Paper</topic><topic>Physical Chemistry</topic><topic>Polycaprolactone</topic><topic>Polymer Sciences</topic><topic>Polymerization</topic><topic>Polymers</topic><topic>Reaction time</topic><topic>Soft and Granular Matter</topic><topic>Software</topic><topic>Tissue engineering</topic><topic>Toluene</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chakraborty, Soma</creatorcontrib><creatorcontrib>Pagaduan, James Nicolas M.</creatorcontrib><creatorcontrib>Melgar, Zara Kryzel A.</creatorcontrib><creatorcontrib>Seitz, Steffen</creatorcontrib><creatorcontrib>Kan, Kai</creatorcontrib><creatorcontrib>Ajiro, Hiroharu</creatorcontrib><collection>CrossRef</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central</collection><collection>SciTech Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>Materials Science Database</collection><collection>Materials science collection</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><jtitle>Polymer bulletin (Berlin, Germany)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chakraborty, Soma</au><au>Pagaduan, James Nicolas M.</au><au>Melgar, Zara Kryzel A.</au><au>Seitz, Steffen</au><au>Kan, Kai</au><au>Ajiro, Hiroharu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Glycerol-modified poly(ε-caprolactone): an biocatalytic approach to improve the hydrophilicity of poly(ε-caprolactone)</atitle><jtitle>Polymer bulletin (Berlin, Germany)</jtitle><stitle>Polym. Bull</stitle><date>2019-04-01</date><risdate>2019</risdate><volume>76</volume><issue>4</issue><spage>1915</spage><epage>1928</epage><pages>1915-1928</pages><issn>0170-0839</issn><eissn>1436-2449</eissn><abstract>Novel poly(ε-caprolactone) (PCL)–glycerol polyester was synthesized in one step in the presence of Novozym 435 under mild reaction conditions. The objective of the study was to investigate the feasibility of enhancing the hydrophilicity of PCL by condensing it with glycerol through biocatalytic approach. Effect of reaction time, glycerol-to-CL ratio and CL-to-toluene ratio was studied. The
1
H NMR and GPC results established that self-condensation of CL units and condensation of CL with glycerol units take place simultaneously. When the glycerol content was 10 and 20 mol% with regard to CL, condensation continued for 6 h; further extension of reaction time resulted in the cleavage of ester linkages. When the glycerol content was increased to 40 mol%, the condensation of CL–glycerol units was accomplished in 4 h; however, the reaction had to get extended beyond 6 h for complete condensation of CL–CL units. The study revealed that the crystallinity and the melting temperature (
T
m
) of the products altered with an increase in the glycerol content. Furthermore, TGA and contact angle values of water on PCL and its glycerol derivative films revealed that the water uptake capacity of PCL too increased significantly with the increase in glycerol content, rendering PCL more hydrophilic.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><doi>10.1007/s00289-018-2443-6</doi><tpages>14</tpages></addata></record> |
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subjects | Characterization and Evaluation of Materials Chemistry Chemistry and Materials Science Complex Fluids and Microfluidics Condensates Contact angle Glycerol Hydrophilicity Melt temperature Molecular weight NMR Nuclear magnetic resonance Organic Chemistry Original Paper Physical Chemistry Polycaprolactone Polymer Sciences Polymerization Polymers Reaction time Soft and Granular Matter Software Tissue engineering Toluene |
title | Glycerol-modified poly(ε-caprolactone): an biocatalytic approach to improve the hydrophilicity of poly(ε-caprolactone) |
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