Ruoxuan Miao, Yuhan Ding, Jie Liu, Jianyu Liu, Zhirong Xin* and Chunyang Bao*,
{"title":"机械坚固、化学可回收的聚(β-氨基酯)基热固性塑料","authors":"Ruoxuan Miao, Yuhan Ding, Jie Liu, Jianyu Liu, Zhirong Xin* and Chunyang Bao*, ","doi":"10.1021/acsapm.4c0294510.1021/acsapm.4c02945","DOIUrl":null,"url":null,"abstract":"<p >The development of chemically recyclable thermosetting plastics using dynamic covalent bonds is of great importance in the construction of a sustainable society. However, there remains a bottleneck barrier in fabricating dynamic covalent thermosetting plastics with simultaneously high mechanical strength, thermal and dimensional stability, and room-temperature chemical recyclability. Herein, a series of poly(β-amino esters) (PBAEs)-based thermosetting plastics with high mechanical strength, desirable dimensional stability, and room-temperature chemical recyclability were fabricated through the aza-Michael addition reaction of bisphenol A glycerolate diacrylate (BG), poly(propylene glycol) bis(2-aminopropyl ether) (PPG), and adipic acid dihydrazide (ADH). By increasing the molar ratios of ADH, the mechanical properties of PBAE-based thermosetting plastics can be scientifically enhanced via the increase of the cross-linking densities and hydrogen bond contents in the polymer networks. Typically, the tensile strength and Young’s modulus of PBAE<sub>5</sub> can be improved to 4.5 and 10.6 times of PBAE<sub>1</sub>, respectively. Meanwhile, based on the rigid polymer network structures, PBAE-based thermosetting plastics exhibited very small creep strain at evaluated temperatures. More importantly, PBAEs-based thermosetting plastics can be easily depolymerized into value-added monomers in an alkaline aqueous solution at room temperature through the hydrolysis of β-amino esters. Therefore, systematically tailoring the cross-linking density and hydrogen bond contents of the polymer network is an efficient and feasible strategy to construct mechanically strong and dimensional stable dynamic covalent thermosetting plastics with room-temperature chemical recyclability.</p>","PeriodicalId":7,"journal":{"name":"ACS Applied Polymer Materials","volume":"6 21","pages":"13439–13448 13439–13448"},"PeriodicalIF":4.7000,"publicationDate":"2024-10-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Mechanically Robust and Chemically Recyclable Poly(β-Amino Esters)-Based Thermosetting Plastics\",\"authors\":\"Ruoxuan Miao, Yuhan Ding, Jie Liu, Jianyu Liu, Zhirong Xin* and Chunyang Bao*, \",\"doi\":\"10.1021/acsapm.4c0294510.1021/acsapm.4c02945\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >The development of chemically recyclable thermosetting plastics using dynamic covalent bonds is of great importance in the construction of a sustainable society. However, there remains a bottleneck barrier in fabricating dynamic covalent thermosetting plastics with simultaneously high mechanical strength, thermal and dimensional stability, and room-temperature chemical recyclability. Herein, a series of poly(β-amino esters) (PBAEs)-based thermosetting plastics with high mechanical strength, desirable dimensional stability, and room-temperature chemical recyclability were fabricated through the aza-Michael addition reaction of bisphenol A glycerolate diacrylate (BG), poly(propylene glycol) bis(2-aminopropyl ether) (PPG), and adipic acid dihydrazide (ADH). By increasing the molar ratios of ADH, the mechanical properties of PBAE-based thermosetting plastics can be scientifically enhanced via the increase of the cross-linking densities and hydrogen bond contents in the polymer networks. Typically, the tensile strength and Young’s modulus of PBAE<sub>5</sub> can be improved to 4.5 and 10.6 times of PBAE<sub>1</sub>, respectively. Meanwhile, based on the rigid polymer network structures, PBAE-based thermosetting plastics exhibited very small creep strain at evaluated temperatures. More importantly, PBAEs-based thermosetting plastics can be easily depolymerized into value-added monomers in an alkaline aqueous solution at room temperature through the hydrolysis of β-amino esters. Therefore, systematically tailoring the cross-linking density and hydrogen bond contents of the polymer network is an efficient and feasible strategy to construct mechanically strong and dimensional stable dynamic covalent thermosetting plastics with room-temperature chemical recyclability.</p>\",\"PeriodicalId\":7,\"journal\":{\"name\":\"ACS Applied Polymer Materials\",\"volume\":\"6 21\",\"pages\":\"13439–13448 13439–13448\"},\"PeriodicalIF\":4.7000,\"publicationDate\":\"2024-10-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Applied Polymer Materials\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acsapm.4c02945\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MATERIALS SCIENCE, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Polymer Materials","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acsapm.4c02945","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
Mechanically Robust and Chemically Recyclable Poly(β-Amino Esters)-Based Thermosetting Plastics
The development of chemically recyclable thermosetting plastics using dynamic covalent bonds is of great importance in the construction of a sustainable society. However, there remains a bottleneck barrier in fabricating dynamic covalent thermosetting plastics with simultaneously high mechanical strength, thermal and dimensional stability, and room-temperature chemical recyclability. Herein, a series of poly(β-amino esters) (PBAEs)-based thermosetting plastics with high mechanical strength, desirable dimensional stability, and room-temperature chemical recyclability were fabricated through the aza-Michael addition reaction of bisphenol A glycerolate diacrylate (BG), poly(propylene glycol) bis(2-aminopropyl ether) (PPG), and adipic acid dihydrazide (ADH). By increasing the molar ratios of ADH, the mechanical properties of PBAE-based thermosetting plastics can be scientifically enhanced via the increase of the cross-linking densities and hydrogen bond contents in the polymer networks. Typically, the tensile strength and Young’s modulus of PBAE5 can be improved to 4.5 and 10.6 times of PBAE1, respectively. Meanwhile, based on the rigid polymer network structures, PBAE-based thermosetting plastics exhibited very small creep strain at evaluated temperatures. More importantly, PBAEs-based thermosetting plastics can be easily depolymerized into value-added monomers in an alkaline aqueous solution at room temperature through the hydrolysis of β-amino esters. Therefore, systematically tailoring the cross-linking density and hydrogen bond contents of the polymer network is an efficient and feasible strategy to construct mechanically strong and dimensional stable dynamic covalent thermosetting plastics with room-temperature chemical recyclability.
期刊介绍:
ACS Applied Polymer Materials is an interdisciplinary journal publishing original research covering all aspects of engineering, chemistry, physics, and biology relevant to applications of polymers.
The journal is devoted to reports of new and original experimental and theoretical research of an applied nature that integrates fundamental knowledge in the areas of materials, engineering, physics, bioscience, polymer science and chemistry into important polymer applications. The journal is specifically interested in work that addresses relationships among structure, processing, morphology, chemistry, properties, and function as well as work that provide insights into mechanisms critical to the performance of the polymer for applications.