Oligomeric ricinoleic acid synthesis with a recyclable catalyst and application to preparing non-isocyanate polyhydroxyurethane

[Display omitted] •A series of ricinoleic acid based non-isocyanate polyurethanes were fabricated.•Oligomeric ricinoleic acid (ORA) was designed as the key intermediate.•SnO was developed as an efficient and recyclable catalyst to access the ORA.•The polymerization degree of ORA can be regulated by...

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Veröffentlicht in:European polymer journal 2021-06, Vol.153, p.110501, Article 110501
Hauptverfasser: Ren, Fang-Yu, You, Fei, Gao, Song, Xie, Wei-Hang, He, Liang-Nian, Li, Hong-Ru
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container_start_page 110501
container_title European polymer journal
container_volume 153
creator Ren, Fang-Yu
You, Fei
Gao, Song
Xie, Wei-Hang
He, Liang-Nian
Li, Hong-Ru
description [Display omitted] •A series of ricinoleic acid based non-isocyanate polyurethanes were fabricated.•Oligomeric ricinoleic acid (ORA) was designed as the key intermediate.•SnO was developed as an efficient and recyclable catalyst to access the ORA.•The polymerization degree of ORA can be regulated by reaction time.•The properties of polyurethanes can be altered by the polymerization degree of ORA. As a consequence of the great demand and extended application of polyurethanes in various fields, the development of green processes for their production and functional polyurethane materials has received widespread attention. In this regard, the biomass-derived polyurethane via the non-isocyanate route could be promising. In this work, the castor-based polyurethanes were designed and synthesized through a non-isocyanate route by employing ricinoleic acid as the starting material, in which the oligomeric ricinoleic acid (ORA) with variable average polymerization degree was used as the key intermediate. To access the ORA with different average polymerization degree, the solid Lewis acid tin(II) oxide (SnO) was developed as the efficient and recyclable catalyst and the average polymerization degree of ORA was regulated by the reaction time at 210 °C. After sequential esterification, epoxidation, cycloaddition with CO2 and polyaddition with 1,6-hexamethylene diamine (HMDA) or isophorone diamine (IPDA), a series of polyhydroxyurethanes (PHUs) with different tensile strength and elongation at break as well as the thermal stability and the glass transition temperature were obtained depending on the type of diamine and the average polymerization degree of ORA, indicating the functional role of the polymerization degree of ORA in regulating the mechanical and thermal properties of the resulting materials. This protocol for the castor-based PHUs preparation in this work not only represents a green and sustainable way to produce bio-based material, but also provides a convenient way to change the average polymerization degree of ORA and then alter the properties of resulting polyurethanes.
doi_str_mv 10.1016/j.eurpolymj.2021.110501
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As a consequence of the great demand and extended application of polyurethanes in various fields, the development of green processes for their production and functional polyurethane materials has received widespread attention. In this regard, the biomass-derived polyurethane via the non-isocyanate route could be promising. In this work, the castor-based polyurethanes were designed and synthesized through a non-isocyanate route by employing ricinoleic acid as the starting material, in which the oligomeric ricinoleic acid (ORA) with variable average polymerization degree was used as the key intermediate. To access the ORA with different average polymerization degree, the solid Lewis acid tin(II) oxide (SnO) was developed as the efficient and recyclable catalyst and the average polymerization degree of ORA was regulated by the reaction time at 210 °C. After sequential esterification, epoxidation, cycloaddition with CO2 and polyaddition with 1,6-hexamethylene diamine (HMDA) or isophorone diamine (IPDA), a series of polyhydroxyurethanes (PHUs) with different tensile strength and elongation at break as well as the thermal stability and the glass transition temperature were obtained depending on the type of diamine and the average polymerization degree of ORA, indicating the functional role of the polymerization degree of ORA in regulating the mechanical and thermal properties of the resulting materials. 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After sequential esterification, epoxidation, cycloaddition with CO2 and polyaddition with 1,6-hexamethylene diamine (HMDA) or isophorone diamine (IPDA), a series of polyhydroxyurethanes (PHUs) with different tensile strength and elongation at break as well as the thermal stability and the glass transition temperature were obtained depending on the type of diamine and the average polymerization degree of ORA, indicating the functional role of the polymerization degree of ORA in regulating the mechanical and thermal properties of the resulting materials. 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You, Fei ; Gao, Song ; Xie, Wei-Hang ; He, Liang-Nian ; Li, Hong-Ru</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c343t-87672a3d8ba9ba5f3a5be37917613c7ed08228bf7fb99afff125c2d5a63d214a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Biological materials</topic><topic>Biomass conversion</topic><topic>Catalysts</topic><topic>Chemical synthesis</topic><topic>Cycloaddition</topic><topic>Diamines</topic><topic>Elongation</topic><topic>Epoxidation</topic><topic>Esterification</topic><topic>Glass transition temperature</topic><topic>Heterogeneous catalysis</topic><topic>Isocyanates</topic><topic>Lewis acid</topic><topic>Non-isocyanate route</topic><topic>Polyhydroxyurethanes</topic><topic>Polymerization</topic><topic>Polyurethane</topic><topic>Polyurethane resins</topic><topic>Reaction time</topic><topic>Ricinoleic acid</topic><topic>Sustainable development</topic><topic>Tensile strength</topic><topic>Thermal stability</topic><topic>Thermodynamic properties</topic><topic>Tin oxides</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ren, Fang-Yu</creatorcontrib><creatorcontrib>You, Fei</creatorcontrib><creatorcontrib>Gao, Song</creatorcontrib><creatorcontrib>Xie, Wei-Hang</creatorcontrib><creatorcontrib>He, Liang-Nian</creatorcontrib><creatorcontrib>Li, Hong-Ru</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>Ren, Fang-Yu</au><au>You, Fei</au><au>Gao, Song</au><au>Xie, Wei-Hang</au><au>He, Liang-Nian</au><au>Li, Hong-Ru</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Oligomeric ricinoleic acid synthesis with a recyclable catalyst and application to preparing non-isocyanate polyhydroxyurethane</atitle><jtitle>European polymer journal</jtitle><date>2021-06-15</date><risdate>2021</risdate><volume>153</volume><spage>110501</spage><pages>110501-</pages><artnum>110501</artnum><issn>0014-3057</issn><eissn>1873-1945</eissn><abstract>[Display omitted] •A series of ricinoleic acid based non-isocyanate polyurethanes were fabricated.•Oligomeric ricinoleic acid (ORA) was designed as the key intermediate.•SnO was developed as an efficient and recyclable catalyst to access the ORA.•The polymerization degree of ORA can be regulated by reaction time.•The properties of polyurethanes can be altered by the polymerization degree of ORA. 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After sequential esterification, epoxidation, cycloaddition with CO2 and polyaddition with 1,6-hexamethylene diamine (HMDA) or isophorone diamine (IPDA), a series of polyhydroxyurethanes (PHUs) with different tensile strength and elongation at break as well as the thermal stability and the glass transition temperature were obtained depending on the type of diamine and the average polymerization degree of ORA, indicating the functional role of the polymerization degree of ORA in regulating the mechanical and thermal properties of the resulting materials. 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ispartof European polymer journal, 2021-06, Vol.153, p.110501, Article 110501
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source Elsevier ScienceDirect Journals
subjects Biological materials
Biomass conversion
Catalysts
Chemical synthesis
Cycloaddition
Diamines
Elongation
Epoxidation
Esterification
Glass transition temperature
Heterogeneous catalysis
Isocyanates
Lewis acid
Non-isocyanate route
Polyhydroxyurethanes
Polymerization
Polyurethane
Polyurethane resins
Reaction time
Ricinoleic acid
Sustainable development
Tensile strength
Thermal stability
Thermodynamic properties
Tin oxides
title Oligomeric ricinoleic acid synthesis with a recyclable catalyst and application to preparing non-isocyanate polyhydroxyurethane
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