木质纤维素基聚3-丙基二丁烯- co -呋喃酸酯的合成:取代己二酸酯。

IF 4.6 2区 化学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Molecules Pub Date : 2025-02-14 DOI:10.3390/molecules30040878
Ruijia Hu, Weihao Li, Xi Zhou, Shunmin Yi, Xingfu Zheng, Qiufeng Mo, Wanyu Liu
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引用次数: 0

摘要

以3-丙二酸(3PAA)、1,4-丁二醇(BDO)和2,5-呋喃二甲酸(FDCA)为原料,合成了新型木质纤维素基聚3-丙二酸丁二醇-呋喃二酸酯(PBApF)。通过1H NMR、GPC、DSC、TGA、XRD、DMA、旋转流变学、拉伸试验和酶降解试验对共聚酯进行了表征。它们是随机的共聚物,其组成得到了很好的控制,共聚酯的数平均序列长度在1.35-4.33之间。结合拉伸试验和DMA结果,PBApF45的断裂伸长率(1865%)远高于PBAF45的断裂伸长率(1250%),即加入线状聚合物的分支增加了熔体强度,赋予了拉伸硬化性能,这有助于提高聚合物的伸长率。此外,从失重角度研究了3PAA含量对酶解的影响;当3PAA含量为55 mol%时,共聚酯具有良好的生物降解性。因此,根据其组成,PBApFS可能最终应用于生物可降解弹性体或其他聚合物的冲击改性剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Synthesis of Lignocellulose-Based Poly(Butylene 3-Propyladipate-Co-Furanoate): Replacing Adipate.

A novel lignocellulose-based poly(butylene 3-propyladipate-co-furanoate) (PBApF) was synthesized from lignocellulose-derived 3-propyladipic acid (3PAA), 1,4-butanediol (BDO), and 2,5-furandicarboxylic acid (FDCA). The copolyesters were characterized by 1H NMR, GPC, DSC, TGA, XRD, DMA, rotational rheology, tensile tests, and enzymatic degradation tests. They were random copolymers whose composition was well controlled, and the number-average sequence lengths of the copolyesters were around 1.35-4.33. By combining the results of tensile tests and DMA, the elongation at break of PBApF45 (1865%) had a much greater value than that of PBAF45 (1250%), i.e., the branching incorporated into the linear polymer increased the melt strength and conferred tension-hardening properties, which helped to enhance the elongation of the polymer. In addition, the influences of 3PAA content on enzymatic degradation were studied in terms of weight loss; when the content of 3PAA was 55 mol%, the copolyesters exhibited good biodegradability. Thus, depending on their composition, PBApFS might find end applications as biodegradable elastomers or impact modifiers for other polymers.

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来源期刊
Molecules
Molecules 化学-有机化学
CiteScore
7.40
自引率
8.70%
发文量
7524
审稿时长
1.4 months
期刊介绍: Molecules (ISSN 1420-3049, CODEN: MOLEFW) is an open access journal of synthetic organic chemistry and natural product chemistry. All articles are peer-reviewed and published continously upon acceptance. Molecules is published by MDPI, Basel, Switzerland. Our aim is to encourage chemists to publish as much as possible their experimental detail, particularly synthetic procedures and characterization information. There is no restriction on the length of the experimental section. In addition, availability of compound samples is published and considered as important information. Authors are encouraged to register or deposit their chemical samples through the non-profit international organization Molecular Diversity Preservation International (MDPI). Molecules has been launched in 1996 to preserve and exploit molecular diversity of both, chemical information and chemical substances.
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