Demonstration of a Chemical Recycling Concept for Polybutylene Succinate containing Waste Substrates via Coupled Enzymatic/Electrochemical Processes.

IF 7.5 2区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
ChemSusChem Pub Date : 2025-01-31 DOI:10.1002/cssc.202402515
Richard Buchinger, Sabrina Bischof, Ole Nickel, Vanessa Grassi, Jasmin Antony, Markus Ostermann, Soniya Gahlawat, Markus Valtiner, Robert Meißner, Georg Gübitz, Christian M Pichler
{"title":"Demonstration of a Chemical Recycling Concept for Polybutylene Succinate containing Waste Substrates via Coupled Enzymatic/Electrochemical Processes.","authors":"Richard Buchinger, Sabrina Bischof, Ole Nickel, Vanessa Grassi, Jasmin Antony, Markus Ostermann, Soniya Gahlawat, Markus Valtiner, Robert Meißner, Georg Gübitz, Christian M Pichler","doi":"10.1002/cssc.202402515","DOIUrl":null,"url":null,"abstract":"<p><p>Chemical recycling of polymer waste is a promising strategy to reduce the dependency of chemical industry on fossil resources and reduce the increasing quantities of plastic waste. A common challenge in chemical recycling processes is the costly downstream separation of reaction products. For polybutylene succinate (PBS) no effective recycling concept has been implemented so far. In this work we demonstrate a promising recycling concept for PBS, avoiding costly purification steps. We developed a sequential process, coupling enzymatic hydrolysis of PBS with an electrochemical reaction step. The enzymatic step efficiently hydrolyses PBS in its monomers, succinic acid and 1,4-butandiol. The electrochemical step converts succinic acid into ethene as final product. Ethene is easily separated from the reaction solution as gaseous product, together with hydrogen as secondary product, while 1,4-butandiol remains in the aqueous solution. Both reaction steps operate in aqueous solvent and benign reaction conditions. Furthermore, the influence of electrolyte components on the electrochemical step was unraveled by applying molecular dynamic simulations. The final coupled process achieves a total ethene productivity of 91 µmol/cm2 over a duration of 8 hours, with 1110 µmol/cm2 hydrogen and 77% regained 1,4-butandiol as valuable secondary products.</p>","PeriodicalId":149,"journal":{"name":"ChemSusChem","volume":" ","pages":"e202402515"},"PeriodicalIF":7.5000,"publicationDate":"2025-01-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ChemSusChem","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1002/cssc.202402515","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

Chemical recycling of polymer waste is a promising strategy to reduce the dependency of chemical industry on fossil resources and reduce the increasing quantities of plastic waste. A common challenge in chemical recycling processes is the costly downstream separation of reaction products. For polybutylene succinate (PBS) no effective recycling concept has been implemented so far. In this work we demonstrate a promising recycling concept for PBS, avoiding costly purification steps. We developed a sequential process, coupling enzymatic hydrolysis of PBS with an electrochemical reaction step. The enzymatic step efficiently hydrolyses PBS in its monomers, succinic acid and 1,4-butandiol. The electrochemical step converts succinic acid into ethene as final product. Ethene is easily separated from the reaction solution as gaseous product, together with hydrogen as secondary product, while 1,4-butandiol remains in the aqueous solution. Both reaction steps operate in aqueous solvent and benign reaction conditions. Furthermore, the influence of electrolyte components on the electrochemical step was unraveled by applying molecular dynamic simulations. The final coupled process achieves a total ethene productivity of 91 µmol/cm2 over a duration of 8 hours, with 1110 µmol/cm2 hydrogen and 77% regained 1,4-butandiol as valuable secondary products.

求助全文
约1分钟内获得全文 求助全文
来源期刊
ChemSusChem
ChemSusChem 化学-化学综合
CiteScore
15.80
自引率
4.80%
发文量
555
审稿时长
1.8 months
期刊介绍: ChemSusChem Impact Factor (2016): 7.226 Scope: Interdisciplinary journal Focuses on research at the interface of chemistry and sustainability Features the best research on sustainability and energy Areas Covered: Chemistry Materials Science Chemical Engineering Biotechnology
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信