Biopolyester prepared using unsaturated betulin (betulinol) extracted from outer birch bark and dicarboxylic acid dichlorides and its thermal-induced crosslinking
Preparation of aliphatic biopolyester using betulin (white birch bark) and acid chloride (Ricinus seed), and its thermally cross-linking. [Display omitted] •Betulin with two hydroxyl moieties and an isopropenyl moiety, extracted from outer birch bark, and aliphatic acid dichlorides were stoichometri...
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description | Preparation of aliphatic biopolyester using betulin (white birch bark) and acid chloride (Ricinus seed), and its thermally cross-linking.
[Display omitted]
•Betulin with two hydroxyl moieties and an isopropenyl moiety, extracted from outer birch bark, and aliphatic acid dichlorides were stoichometrically polycondensated to give the corresponding biopolyesters in high yields at a room temperature.•In the case of sebacoyl chloride, which was derived from sebacic acid involved in castor oil of Ricinus seed, the polymerization yield reached approximately 91%.•The isopropenyl moiety, attached to the betulin mother molecule in the polymer, worked as the cross-linker by heating under a nitrogen atmosphere.•This thermal treatment gave not only almost cross-linked insoluble polymer in organic solvents but also the heat-resistant polymer with Tg, 150 °C.
Betulin, also called betulinol, with two hydroxyl moieties extracted from white birch bark, and acid dichloride (ClCO(CH2)mCOCl) were successfully polycondensed to give the corresponding aliphatic biopolyester (ABIOS) in the presence of pyridine; in particular, in the case of sebacoyl dichloride (m = 8), derived from sebacic acid contained in castor oil of Ricinus seed, the ABIOS8 was obtained in a fairly high yield of 91%, with Mw = ∼23,800 and Mw/Mn = ∼2.1, even at room temperature. By contrast, the polymerization using other acid dichlorides with short methylene chains, i.e., m = 2, 4, 5, and 7, and long methylene chains, i.e., m = 10, resulted in relatively lower yields with a lower molecular weight, Mw. The ABIOS8 with (CH2)8 showed a high glass transition temperature (Tg ≈ 150 °C) superior to that of polylactic acid (PLA) known as a typical biopolyester. A colorless transparent film of ABIOS8 was easily fabricated by the solvent-casting method using THF or CHCl3 as solvent. Furthermore, the ABIOS8 gradually became insoluble in solvents such as THF when heated to 250 °C even under a nitrogen atmosphere. It was deduced that the CC bond in the isopropenyl moiety (H2CC(CH3)) as the third substituent within the betulin mother molecule in ABIOS8 acted as a thermally induced cross-linker. |
doi_str_mv | 10.1016/j.eurpolymj.2019.01.038 |
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[Display omitted]
•Betulin with two hydroxyl moieties and an isopropenyl moiety, extracted from outer birch bark, and aliphatic acid dichlorides were stoichometrically polycondensated to give the corresponding biopolyesters in high yields at a room temperature.•In the case of sebacoyl chloride, which was derived from sebacic acid involved in castor oil of Ricinus seed, the polymerization yield reached approximately 91%.•The isopropenyl moiety, attached to the betulin mother molecule in the polymer, worked as the cross-linker by heating under a nitrogen atmosphere.•This thermal treatment gave not only almost cross-linked insoluble polymer in organic solvents but also the heat-resistant polymer with Tg, 150 °C.
Betulin, also called betulinol, with two hydroxyl moieties extracted from white birch bark, and acid dichloride (ClCO(CH2)mCOCl) were successfully polycondensed to give the corresponding aliphatic biopolyester (ABIOS) in the presence of pyridine; in particular, in the case of sebacoyl dichloride (m = 8), derived from sebacic acid contained in castor oil of Ricinus seed, the ABIOS8 was obtained in a fairly high yield of 91%, with Mw = ∼23,800 and Mw/Mn = ∼2.1, even at room temperature. By contrast, the polymerization using other acid dichlorides with short methylene chains, i.e., m = 2, 4, 5, and 7, and long methylene chains, i.e., m = 10, resulted in relatively lower yields with a lower molecular weight, Mw. The ABIOS8 with (CH2)8 showed a high glass transition temperature (Tg ≈ 150 °C) superior to that of polylactic acid (PLA) known as a typical biopolyester. A colorless transparent film of ABIOS8 was easily fabricated by the solvent-casting method using THF or CHCl3 as solvent. Furthermore, the ABIOS8 gradually became insoluble in solvents such as THF when heated to 250 °C even under a nitrogen atmosphere. It was deduced that the CC bond in the isopropenyl moiety (H2CC(CH3)) as the third substituent within the betulin mother molecule in ABIOS8 acted as a thermally induced cross-linker.</description><identifier>ISSN: 0014-3057</identifier><identifier>EISSN: 1873-1945</identifier><identifier>DOI: 10.1016/j.eurpolymj.2019.01.038</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Aliphatic compounds ; Bark ; Bayh, Birch ; Betulin ; Biopolyester ; Castor oil ; Chloroform ; Cross-linking ; Crosslinking ; Dichlorides ; Glass transition temperature ; Heat-resistant polymer ; Methylene ; Molecular weight ; Polylactic acid ; Polymerization ; Sebacic acid ; Solvents ; Temperature</subject><ispartof>European polymer journal, 2019-04, Vol.113, p.12-17</ispartof><rights>2019 Elsevier Ltd</rights><rights>Copyright Elsevier BV Apr 2019</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c380t-4bc38b145aeee38ccb5cc55005cb9e9ac6e7519f1374f72059039ce669d24ae63</citedby><cites>FETCH-LOGICAL-c380t-4bc38b145aeee38ccb5cc55005cb9e9ac6e7519f1374f72059039ce669d24ae63</cites><orcidid>0000-0003-3384-9847 ; 0000-0001-6575-045X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0014305718319773$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids></links><search><creatorcontrib>Okada, Masuhiro</creatorcontrib><creatorcontrib>Suzuki, Katsunori</creatorcontrib><creatorcontrib>Mawatari, Yasuteru</creatorcontrib><creatorcontrib>Tabata, Masayoshi</creatorcontrib><title>Biopolyester prepared using unsaturated betulin (betulinol) extracted from outer birch bark and dicarboxylic acid dichlorides and its thermal-induced crosslinking</title><title>European polymer journal</title><description>Preparation of aliphatic biopolyester using betulin (white birch bark) and acid chloride (Ricinus seed), and its thermally cross-linking.
[Display omitted]
•Betulin with two hydroxyl moieties and an isopropenyl moiety, extracted from outer birch bark, and aliphatic acid dichlorides were stoichometrically polycondensated to give the corresponding biopolyesters in high yields at a room temperature.•In the case of sebacoyl chloride, which was derived from sebacic acid involved in castor oil of Ricinus seed, the polymerization yield reached approximately 91%.•The isopropenyl moiety, attached to the betulin mother molecule in the polymer, worked as the cross-linker by heating under a nitrogen atmosphere.•This thermal treatment gave not only almost cross-linked insoluble polymer in organic solvents but also the heat-resistant polymer with Tg, 150 °C.
Betulin, also called betulinol, with two hydroxyl moieties extracted from white birch bark, and acid dichloride (ClCO(CH2)mCOCl) were successfully polycondensed to give the corresponding aliphatic biopolyester (ABIOS) in the presence of pyridine; in particular, in the case of sebacoyl dichloride (m = 8), derived from sebacic acid contained in castor oil of Ricinus seed, the ABIOS8 was obtained in a fairly high yield of 91%, with Mw = ∼23,800 and Mw/Mn = ∼2.1, even at room temperature. By contrast, the polymerization using other acid dichlorides with short methylene chains, i.e., m = 2, 4, 5, and 7, and long methylene chains, i.e., m = 10, resulted in relatively lower yields with a lower molecular weight, Mw. The ABIOS8 with (CH2)8 showed a high glass transition temperature (Tg ≈ 150 °C) superior to that of polylactic acid (PLA) known as a typical biopolyester. A colorless transparent film of ABIOS8 was easily fabricated by the solvent-casting method using THF or CHCl3 as solvent. Furthermore, the ABIOS8 gradually became insoluble in solvents such as THF when heated to 250 °C even under a nitrogen atmosphere. It was deduced that the CC bond in the isopropenyl moiety (H2CC(CH3)) as the third substituent within the betulin mother molecule in ABIOS8 acted as a thermally induced cross-linker.</description><subject>Aliphatic compounds</subject><subject>Bark</subject><subject>Bayh, Birch</subject><subject>Betulin</subject><subject>Biopolyester</subject><subject>Castor oil</subject><subject>Chloroform</subject><subject>Cross-linking</subject><subject>Crosslinking</subject><subject>Dichlorides</subject><subject>Glass transition temperature</subject><subject>Heat-resistant polymer</subject><subject>Methylene</subject><subject>Molecular weight</subject><subject>Polylactic acid</subject><subject>Polymerization</subject><subject>Sebacic acid</subject><subject>Solvents</subject><subject>Temperature</subject><issn>0014-3057</issn><issn>1873-1945</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNqFUcuO1DAQjBBIDAvfgCUucEi2bcfJ5LiseEkrcYGz5TgdxtlMHNo22vkdvhRnZsV1T93qrqp-VFG85VBx4M31VGGi1c-n41QJ4F0FvAK5f1bs-L6VJe9q9bzYAfC6lKDal8WrECYAaGUjd8Xfj85vZAwRia2EqyEcWApu-cXSEkxMZGKu9BjT7Bb2_jHx8weGD5GM3boj-SPzadPoHdkD6w3dM7MMbHDWUO8fTrOzzFh3rhxmT27AcEa4GFg8IB3NXLplSDbrWfIh5Cn3eY3XxYvRzAHfPMar4ufnTz9uv5Z33798u725K63cQyzrPsee18ogotxb2ytrlQJQtu-wM7bBVvFu5LKtx1aA6kB2FpumG0RtsJFXxbuL7kr-d8oP0ZNPtOSRWgjBhagF31DtBXVekXDUK7mjoZPmoDdD9KT_G6I3QzRwnQ3JzJsLE_MRfxySDtbhks91hDbqwbsnNf4BMZyeEA</recordid><startdate>20190401</startdate><enddate>20190401</enddate><creator>Okada, Masuhiro</creator><creator>Suzuki, Katsunori</creator><creator>Mawatari, Yasuteru</creator><creator>Tabata, Masayoshi</creator><general>Elsevier Ltd</general><general>Elsevier BV</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8FD</scope><scope>JG9</scope><orcidid>https://orcid.org/0000-0003-3384-9847</orcidid><orcidid>https://orcid.org/0000-0001-6575-045X</orcidid></search><sort><creationdate>20190401</creationdate><title>Biopolyester prepared using unsaturated betulin (betulinol) extracted from outer birch bark and dicarboxylic acid dichlorides and its thermal-induced crosslinking</title><author>Okada, Masuhiro ; Suzuki, Katsunori ; Mawatari, Yasuteru ; Tabata, Masayoshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c380t-4bc38b145aeee38ccb5cc55005cb9e9ac6e7519f1374f72059039ce669d24ae63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Aliphatic compounds</topic><topic>Bark</topic><topic>Bayh, Birch</topic><topic>Betulin</topic><topic>Biopolyester</topic><topic>Castor oil</topic><topic>Chloroform</topic><topic>Cross-linking</topic><topic>Crosslinking</topic><topic>Dichlorides</topic><topic>Glass transition temperature</topic><topic>Heat-resistant polymer</topic><topic>Methylene</topic><topic>Molecular weight</topic><topic>Polylactic acid</topic><topic>Polymerization</topic><topic>Sebacic acid</topic><topic>Solvents</topic><topic>Temperature</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Okada, Masuhiro</creatorcontrib><creatorcontrib>Suzuki, Katsunori</creatorcontrib><creatorcontrib>Mawatari, Yasuteru</creatorcontrib><creatorcontrib>Tabata, Masayoshi</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>European polymer journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Okada, Masuhiro</au><au>Suzuki, Katsunori</au><au>Mawatari, Yasuteru</au><au>Tabata, Masayoshi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Biopolyester prepared using unsaturated betulin (betulinol) extracted from outer birch bark and dicarboxylic acid dichlorides and its thermal-induced crosslinking</atitle><jtitle>European polymer journal</jtitle><date>2019-04-01</date><risdate>2019</risdate><volume>113</volume><spage>12</spage><epage>17</epage><pages>12-17</pages><issn>0014-3057</issn><eissn>1873-1945</eissn><abstract>Preparation of aliphatic biopolyester using betulin (white birch bark) and acid chloride (Ricinus seed), and its thermally cross-linking.
[Display omitted]
•Betulin with two hydroxyl moieties and an isopropenyl moiety, extracted from outer birch bark, and aliphatic acid dichlorides were stoichometrically polycondensated to give the corresponding biopolyesters in high yields at a room temperature.•In the case of sebacoyl chloride, which was derived from sebacic acid involved in castor oil of Ricinus seed, the polymerization yield reached approximately 91%.•The isopropenyl moiety, attached to the betulin mother molecule in the polymer, worked as the cross-linker by heating under a nitrogen atmosphere.•This thermal treatment gave not only almost cross-linked insoluble polymer in organic solvents but also the heat-resistant polymer with Tg, 150 °C.
Betulin, also called betulinol, with two hydroxyl moieties extracted from white birch bark, and acid dichloride (ClCO(CH2)mCOCl) were successfully polycondensed to give the corresponding aliphatic biopolyester (ABIOS) in the presence of pyridine; in particular, in the case of sebacoyl dichloride (m = 8), derived from sebacic acid contained in castor oil of Ricinus seed, the ABIOS8 was obtained in a fairly high yield of 91%, with Mw = ∼23,800 and Mw/Mn = ∼2.1, even at room temperature. By contrast, the polymerization using other acid dichlorides with short methylene chains, i.e., m = 2, 4, 5, and 7, and long methylene chains, i.e., m = 10, resulted in relatively lower yields with a lower molecular weight, Mw. The ABIOS8 with (CH2)8 showed a high glass transition temperature (Tg ≈ 150 °C) superior to that of polylactic acid (PLA) known as a typical biopolyester. A colorless transparent film of ABIOS8 was easily fabricated by the solvent-casting method using THF or CHCl3 as solvent. Furthermore, the ABIOS8 gradually became insoluble in solvents such as THF when heated to 250 °C even under a nitrogen atmosphere. It was deduced that the CC bond in the isopropenyl moiety (H2CC(CH3)) as the third substituent within the betulin mother molecule in ABIOS8 acted as a thermally induced cross-linker.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><doi>10.1016/j.eurpolymj.2019.01.038</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0003-3384-9847</orcidid><orcidid>https://orcid.org/0000-0001-6575-045X</orcidid></addata></record> |
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subjects | Aliphatic compounds Bark Bayh, Birch Betulin Biopolyester Castor oil Chloroform Cross-linking Crosslinking Dichlorides Glass transition temperature Heat-resistant polymer Methylene Molecular weight Polylactic acid Polymerization Sebacic acid Solvents Temperature |
title | Biopolyester prepared using unsaturated betulin (betulinol) extracted from outer birch bark and dicarboxylic acid dichlorides and its thermal-induced crosslinking |
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