Designed for Molecular Recycling: A Lignin-Derived Semi-aromatic Biobased Polymer
The development of chemically recyclable biopolymers offers opportunities within the pursuit of a circular economy. Chemically recyclable biopolymers make a positive effort to solve the issue of polymer materials in the disposal phase after the use phase. In this paper, the production of biobased se...
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creator | Molendijk, Dennis van Beurden, Koen van Schijndel, Jack |
description | The development of chemically recyclable biopolymers offers opportunities within the pursuit of a circular economy. Chemically recyclable biopolymers make a positive effort to solve the issue of polymer materials in the disposal phase after the use phase. In this paper, the production of biobased semi-aromatic polyesters, which can be extracted entirely from biomass such as lignin, is described and visualized. The polymer poly-S described in this paper has thermal properties similar to certain commonly used plastics, such as PET. We developed a Green Knoevenagel reaction, which can efficiently produce monomers from aromatic aldehydes and malonic acid. This reaction has been proven to be scalable and has a remarkably low calculated E-factor. These polyesters with ligno-phytochemicals as a starting point show an efficient molecular recycling with minimal losses. The polyester poly(dihydrosinapinic acid) (poly-S) is presented as an example of these semi-aromatic polyesters, and the polymerization, depolymerization, and re-polymerization are described. |
doi_str_mv | 10.3791/61975 |
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Chemically recyclable biopolymers make a positive effort to solve the issue of polymer materials in the disposal phase after the use phase. In this paper, the production of biobased semi-aromatic polyesters, which can be extracted entirely from biomass such as lignin, is described and visualized. The polymer poly-S described in this paper has thermal properties similar to certain commonly used plastics, such as PET. We developed a Green Knoevenagel reaction, which can efficiently produce monomers from aromatic aldehydes and malonic acid. This reaction has been proven to be scalable and has a remarkably low calculated E-factor. These polyesters with ligno-phytochemicals as a starting point show an efficient molecular recycling with minimal losses. 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Chemically recyclable biopolymers make a positive effort to solve the issue of polymer materials in the disposal phase after the use phase. In this paper, the production of biobased semi-aromatic polyesters, which can be extracted entirely from biomass such as lignin, is described and visualized. The polymer poly-S described in this paper has thermal properties similar to certain commonly used plastics, such as PET. We developed a Green Knoevenagel reaction, which can efficiently produce monomers from aromatic aldehydes and malonic acid. This reaction has been proven to be scalable and has a remarkably low calculated E-factor. These polyesters with ligno-phytochemicals as a starting point show an efficient molecular recycling with minimal losses. The polyester poly(dihydrosinapinic acid) (poly-S) is presented as an example of these semi-aromatic polyesters, and the polymerization, depolymerization, and re-polymerization are described.</description><subject>Acetylation</subject><subject>Alkalies - chemistry</subject><subject>Biomass</subject><subject>Calorimetry, Differential Scanning</subject><subject>Coumaric Acids - chemistry</subject><subject>Hydrogenation</subject><subject>Hydrolysis</subject><subject>Lignin - chemistry</subject><subject>Nickel - chemistry</subject><subject>Polymerization</subject><subject>Proton Magnetic Resonance Spectroscopy</subject><issn>1940-087X</issn><issn>1940-087X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpN0EtLw0AUBeBBFFtr_4JkI7iJzjMz4662vqDiG9yFyeSmjCSZOtMI_fdGW8XVPVw-zuIgNCb4lElNzjKipdhBQ6I5TrGSb7v_8gAdxPiOcUaxUPtowBgjhDM2RI8ziG7RQplUPiR3vgbb1SYkT2DXtnbt4jyZJPNeuDadQXCfvXyGxqUm-MasnE0unC9M7N8Pvl43EA7RXmXqCOPtHaHXq8uX6U06v7--nU7mqaU6W6WcUcEBC-CkULriulRSGSst5lxykglVYV1YagGILq1kuBLGCCI4oZoay0boZNO7DP6jg7jKGxct1LVpwXcxp1xiTBVnqqfHG2qDjzFAlS-Da0xY5wTn3-vlP-v17mhb2RUNlH_qdy72BQ19Z7w</recordid><startdate>20201130</startdate><enddate>20201130</enddate><creator>Molendijk, Dennis</creator><creator>van Beurden, Koen</creator><creator>van Schijndel, Jack</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20201130</creationdate><title>Designed for Molecular Recycling: A Lignin-Derived Semi-aromatic Biobased Polymer</title><author>Molendijk, Dennis ; van Beurden, Koen ; van Schijndel, Jack</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c296t-43254e05e41b89f49d878ac7c044741658f09bc2cee19dc730f5aa51541292ac3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Acetylation</topic><topic>Alkalies - chemistry</topic><topic>Biomass</topic><topic>Calorimetry, Differential Scanning</topic><topic>Coumaric Acids - chemistry</topic><topic>Hydrogenation</topic><topic>Hydrolysis</topic><topic>Lignin - chemistry</topic><topic>Nickel - chemistry</topic><topic>Polymerization</topic><topic>Proton Magnetic Resonance Spectroscopy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Molendijk, Dennis</creatorcontrib><creatorcontrib>van Beurden, Koen</creatorcontrib><creatorcontrib>van Schijndel, Jack</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of visualized experiments</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Molendijk, Dennis</au><au>van Beurden, Koen</au><au>van Schijndel, Jack</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Designed for Molecular Recycling: A Lignin-Derived Semi-aromatic Biobased Polymer</atitle><jtitle>Journal of visualized experiments</jtitle><addtitle>J Vis Exp</addtitle><date>2020-11-30</date><risdate>2020</risdate><issue>165</issue><issn>1940-087X</issn><eissn>1940-087X</eissn><abstract>The development of chemically recyclable biopolymers offers opportunities within the pursuit of a circular economy. Chemically recyclable biopolymers make a positive effort to solve the issue of polymer materials in the disposal phase after the use phase. In this paper, the production of biobased semi-aromatic polyesters, which can be extracted entirely from biomass such as lignin, is described and visualized. The polymer poly-S described in this paper has thermal properties similar to certain commonly used plastics, such as PET. We developed a Green Knoevenagel reaction, which can efficiently produce monomers from aromatic aldehydes and malonic acid. This reaction has been proven to be scalable and has a remarkably low calculated E-factor. These polyesters with ligno-phytochemicals as a starting point show an efficient molecular recycling with minimal losses. The polyester poly(dihydrosinapinic acid) (poly-S) is presented as an example of these semi-aromatic polyesters, and the polymerization, depolymerization, and re-polymerization are described.</abstract><cop>United States</cop><pmid>33311433</pmid><doi>10.3791/61975</doi></addata></record> |
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subjects | Acetylation Alkalies - chemistry Biomass Calorimetry, Differential Scanning Coumaric Acids - chemistry Hydrogenation Hydrolysis Lignin - chemistry Nickel - chemistry Polymerization Proton Magnetic Resonance Spectroscopy |
title | Designed for Molecular Recycling: A Lignin-Derived Semi-aromatic Biobased Polymer |
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