Zhuohao Xia, Baoli Huang, Jiaqi Shen, Yanqin Shi, Huiwen He, Yulu Zhu, Zhaobin Tang, Si Chen, Xu Wang
{"title":"高分子量全生物基半芳香族呋喃聚酰胺的合成及其聚合工艺研究","authors":"Zhuohao Xia, Baoli Huang, Jiaqi Shen, Yanqin Shi, Huiwen He, Yulu Zhu, Zhaobin Tang, Si Chen, Xu Wang","doi":"10.1021/acssuschemeng.4c06026","DOIUrl":null,"url":null,"abstract":"Biobased monomer furan-2,5-dicarboxylic acid (FDCA) can replace terephthalic acid to achieve the synthesis of biobased semiaromatic polyamides, but FDCA has the problem of difficulty in increasing polymer molecular weight due to decarboxylation, which affects material properties. Hence, this study employed a method of synthesizing high-molecular-weight semiaromatic polyamides using FDCA esterification products (DMFD) as raw materials. Although this method reduces the activity of monomers, it improves the stability of monomers and is currently a commonly used method. Therefore, amine-based catalysts that enhance the reaction activity through nucleophilic mechanisms are chosen. A poly(pentamethylene furan amide) (PA5F) series was synthesized by melt polymerization using 2-hydroxypyridine as a catalyst. The product structures at different polymerization stages were studied, and the reaction was inferred. The results showed that pyridine catalysts with a nucleophilic ability improved the polymerization activity of DMFD in the early polymerization stage while avoiding <i>N</i>-methylation of the terminal amino group of the oligomers. At the same time, it was revealed that in the process of ester amine polymerization under pyridine catalysts, the end ester groups of the polymer will react and transform into carboxyl groups. This causes a decarboxylation reaction in the later stage of high-temperature polymerization, resulting in an imbalanced end-group ratio, leading to end-group sealing and limiting the molecular weight increase. Finally, by optimizing the reaction process formula and adding an excess (15 mol %) of pentamethylene diamine (PMD) to the feed, a high-molecular-weight polyamide material with <i>M</i><sub>w</sub> of 150,000 g/mol can be polymerized. The results of this study indicate that pyridine catalysts represented by 2-hydroxypyridine have great potential in the preparation of high-molecular-weight semiaromatic polyamides.","PeriodicalId":25,"journal":{"name":"ACS Sustainable Chemistry & Engineering","volume":"44 1","pages":""},"PeriodicalIF":7.3000,"publicationDate":"2024-10-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synthesis of High-Molecular-Weight All-Biobased Semiaromatic Furan Polyamide and Study on Its Polymerization Process\",\"authors\":\"Zhuohao Xia, Baoli Huang, Jiaqi Shen, Yanqin Shi, Huiwen He, Yulu Zhu, Zhaobin Tang, Si Chen, Xu Wang\",\"doi\":\"10.1021/acssuschemeng.4c06026\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Biobased monomer furan-2,5-dicarboxylic acid (FDCA) can replace terephthalic acid to achieve the synthesis of biobased semiaromatic polyamides, but FDCA has the problem of difficulty in increasing polymer molecular weight due to decarboxylation, which affects material properties. Hence, this study employed a method of synthesizing high-molecular-weight semiaromatic polyamides using FDCA esterification products (DMFD) as raw materials. Although this method reduces the activity of monomers, it improves the stability of monomers and is currently a commonly used method. Therefore, amine-based catalysts that enhance the reaction activity through nucleophilic mechanisms are chosen. A poly(pentamethylene furan amide) (PA5F) series was synthesized by melt polymerization using 2-hydroxypyridine as a catalyst. The product structures at different polymerization stages were studied, and the reaction was inferred. The results showed that pyridine catalysts with a nucleophilic ability improved the polymerization activity of DMFD in the early polymerization stage while avoiding <i>N</i>-methylation of the terminal amino group of the oligomers. At the same time, it was revealed that in the process of ester amine polymerization under pyridine catalysts, the end ester groups of the polymer will react and transform into carboxyl groups. This causes a decarboxylation reaction in the later stage of high-temperature polymerization, resulting in an imbalanced end-group ratio, leading to end-group sealing and limiting the molecular weight increase. Finally, by optimizing the reaction process formula and adding an excess (15 mol %) of pentamethylene diamine (PMD) to the feed, a high-molecular-weight polyamide material with <i>M</i><sub>w</sub> of 150,000 g/mol can be polymerized. The results of this study indicate that pyridine catalysts represented by 2-hydroxypyridine have great potential in the preparation of high-molecular-weight semiaromatic polyamides.\",\"PeriodicalId\":25,\"journal\":{\"name\":\"ACS Sustainable Chemistry & Engineering\",\"volume\":\"44 1\",\"pages\":\"\"},\"PeriodicalIF\":7.3000,\"publicationDate\":\"2024-10-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Sustainable Chemistry & Engineering\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1021/acssuschemeng.4c06026\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Sustainable Chemistry & Engineering","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acssuschemeng.4c06026","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Synthesis of High-Molecular-Weight All-Biobased Semiaromatic Furan Polyamide and Study on Its Polymerization Process
Biobased monomer furan-2,5-dicarboxylic acid (FDCA) can replace terephthalic acid to achieve the synthesis of biobased semiaromatic polyamides, but FDCA has the problem of difficulty in increasing polymer molecular weight due to decarboxylation, which affects material properties. Hence, this study employed a method of synthesizing high-molecular-weight semiaromatic polyamides using FDCA esterification products (DMFD) as raw materials. Although this method reduces the activity of monomers, it improves the stability of monomers and is currently a commonly used method. Therefore, amine-based catalysts that enhance the reaction activity through nucleophilic mechanisms are chosen. A poly(pentamethylene furan amide) (PA5F) series was synthesized by melt polymerization using 2-hydroxypyridine as a catalyst. The product structures at different polymerization stages were studied, and the reaction was inferred. The results showed that pyridine catalysts with a nucleophilic ability improved the polymerization activity of DMFD in the early polymerization stage while avoiding N-methylation of the terminal amino group of the oligomers. At the same time, it was revealed that in the process of ester amine polymerization under pyridine catalysts, the end ester groups of the polymer will react and transform into carboxyl groups. This causes a decarboxylation reaction in the later stage of high-temperature polymerization, resulting in an imbalanced end-group ratio, leading to end-group sealing and limiting the molecular weight increase. Finally, by optimizing the reaction process formula and adding an excess (15 mol %) of pentamethylene diamine (PMD) to the feed, a high-molecular-weight polyamide material with Mw of 150,000 g/mol can be polymerized. The results of this study indicate that pyridine catalysts represented by 2-hydroxypyridine have great potential in the preparation of high-molecular-weight semiaromatic polyamides.
期刊介绍:
ACS Sustainable Chemistry & Engineering is a prestigious weekly peer-reviewed scientific journal published by the American Chemical Society. Dedicated to advancing the principles of green chemistry and green engineering, it covers a wide array of research topics including green chemistry, green engineering, biomass, alternative energy, and life cycle assessment.
The journal welcomes submissions in various formats, including Letters, Articles, Features, and Perspectives (Reviews), that address the challenges of sustainability in the chemical enterprise and contribute to the advancement of sustainable practices. Join us in shaping the future of sustainable chemistry and engineering.