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基于废面粉衍生前驱体的生物基环氧基体的化学循环利用:回收聚合物表征

Chemical Recycling of Bio-Based Epoxy Matrices Based on Precursors Derived from Waste Flour: Recycled Polymers Characterization.

作者信息

Saitta Lorena, Dattilo Sandro, Rizzo Giuliana, Tosto Claudio, Blanco Ignazio, Ferrari Francesca, Carallo Gloria Anna, Cafaro Fabrizio, Greco Antonio, Cicala Gianluca

机构信息

Department of Civil Engineering and Architecture, University of Catania, Via Santa Sofia 64, 95125 Catania, Italy.

CNR-IPCB, Via Paolo Gaifami 18, 95126 Catania, Italy.

出版信息

Polymers (Basel). 2025 Jan 26;17(3):335. doi: 10.3390/polym17030335.

Abstract

This study aims to investigate the chemical recycling of two different fully recyclable bio-based epoxy matrices based on epoxidized precursors derived from waste flour. The key for their recyclability relies on the use of a cleavable hardener. In fact, the latter contains a ketal group in its chemical structure, which is cleavable in mild acetic conditions, so allowing for the breakage of the cured network. The recyclability was successfully assessed for both the two investigated formulations, with a recycling process yield ranging from 80 up to 85%. The recycled polymers presented a up to 69.0 ± 0.4 °C, determined by mean of DMA and DSC analysis. Next, the TGA revealed that the thermal decomposition of the specimens primarily occurred around 320 °C and attributed to the breaking of C-O and C-N bonds in cross-linked networks. In the end, the chemical characterizations were carried out by mean of Py-GC/MS, MALDI-TOF-MS and FT-IR ATR. In fact, these analyses allowed for investigating how the recycled polymer's structure changed, starting from the initial epoxy systems. These insights on their chemical structure could further allow for identifying re-use strategies in accordance with a circular economy approach.

摘要

本研究旨在探讨基于废面粉衍生的环氧化前体的两种不同的完全可回收生物基环氧基体的化学循环利用。它们可回收性的关键在于使用可裂解的固化剂。事实上,后者在其化学结构中含有一个缩酮基团,该基团在温和的醋酸条件下可裂解,从而使固化网络得以破坏。对所研究的两种配方的可回收性均进行了成功评估,回收过程的产率在80%至85%之间。通过动态热机械分析(DMA)和差示扫描量热法(DSC)分析测定,回收的聚合物呈现出高达69.0±0.4℃的[此处原文缺失相关内容]。接下来,热重分析(TGA)表明,样品的热分解主要发生在320℃左右,这归因于交联网络中C-O键和C-N键的断裂。最后,通过热解气相色谱/质谱联用(Py-GC/MS)、基质辅助激光解吸电离飞行时间质谱(MALDI-TOF-MS)和衰减全反射傅里叶变换红外光谱(FT-IR ATR)进行化学表征。事实上,这些分析能够从初始环氧体系出发,研究回收聚合物的结构是如何变化的。对其化学结构的这些见解可以进一步有助于根据循环经济方法确定再利用策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/32f3/11821098/95192e49070f/polymers-17-00335-g001.jpg

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