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通过对可熔融流动的有机溶剂木质素进行甲基丙烯酸缩水甘油酯接枝,提高聚乳酸生物复合材料在高木质素负载量下的性能。

Improved Performance of Polylactic Acid Biocomposites at High Lignin Loadings through Glycidyl Methacrylate Grafting of Melt-Flowable Organosolv Lignin.

作者信息

Alshammari Shallal, Ameli Amir

机构信息

Department of Plastics Engineering, University of Massachusetts Lowell, 1 University Ave, Lowell, Massachusetts 01854, United States.

出版信息

ACS Omega. 2024 Aug 6;9(33):35937-35949. doi: 10.1021/acsomega.4c05212. eCollection 2024 Aug 20.

DOI:10.1021/acsomega.4c05212
PMID:39184474
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11339841/
Abstract

Glycidyl methacrylate (GMA) was grafted onto a melt-flowable organosolv lignin, called bioleum (BL), using a melt mixing process. Then, up to 40 wt % of BL--GMA was blended with polylactic acid (PLA) in the presence of dicumyl peroxide as a free radical initiator utilizing a melt extrusion method. Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis, differential scanning calorimetry, scanning electron microscopy, and tensile testing were performed to characterize the biocomposites' performance. The FTIR results revealed a successful grafting of GMA onto BL. Overall, BL and PLA compatibility increased significantly with the grafting and resulted in decreased domain size of BL--GMA and thus enhanced all the tensile properties (strength, modulus, and elongation at break) at BL loadings as high as 40 wt %. For instance, in the biocomposites containing 30 wt % BL, the GMA grafting increased the tensile strength by 23%. The presence of BL and BL--GMA hindered PLA's crystallization even when it was cooled at a rate of 1 °C/min. However, the composites with BL--GMA showed a crystallinity value comparable to that of PLA during isothermal crystallization, but with a slower crystallization rate. This work reveals a facile and scalable method that can be adopted to enhance the performance of lignin-based biocomposites.

摘要

采用熔融共混工艺将甲基丙烯酸缩水甘油酯(GMA)接枝到一种可熔融流动的有机溶剂木质素(称为生物油(BL))上。然后,在过氧化二异丙苯作为自由基引发剂的存在下,利用熔融挤出法将高达40 wt%的BL - GMA与聚乳酸(PLA)共混。通过傅里叶变换红外光谱(FTIR)、热重分析、差示扫描量热法、扫描电子显微镜和拉伸试验来表征生物复合材料的性能。FTIR结果表明GMA成功接枝到了BL上。总体而言,随着接枝的进行,BL与PLA的相容性显著提高,导致BL - GMA的相畴尺寸减小,从而在BL含量高达40 wt%时提高了所有拉伸性能(强度、模量和断裂伸长率)。例如,在含有30 wt% BL的生物复合材料中,GMA接枝使拉伸强度提高了23%。即使以1℃/min的速率冷却,BL和BL - GMA的存在也会阻碍PLA的结晶。然而,含有BL - GMA的复合材料在等温结晶过程中显示出与PLA相当的结晶度值,但结晶速率较慢。这项工作揭示了一种简便且可扩展的方法,可用于提高木质素基生物复合材料的性能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f674/11339841/5443326233c5/ao4c05212_0010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f674/11339841/8610d085084f/ao4c05212_0001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f674/11339841/ae81aa0dc43a/ao4c05212_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f674/11339841/80044e4f48e4/ao4c05212_0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f674/11339841/4cb52a7d9744/ao4c05212_0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f674/11339841/c9672ddaf615/ao4c05212_0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f674/11339841/5443326233c5/ao4c05212_0010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f674/11339841/8610d085084f/ao4c05212_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f674/11339841/2e630cd0e9a6/ao4c05212_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f674/11339841/51aed89df85e/ao4c05212_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f674/11339841/5d9b21f896e1/ao4c05212_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f674/11339841/3378324c8f7f/ao4c05212_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f674/11339841/ae81aa0dc43a/ao4c05212_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f674/11339841/80044e4f48e4/ao4c05212_0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f674/11339841/4cb52a7d9744/ao4c05212_0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f674/11339841/c9672ddaf615/ao4c05212_0009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f674/11339841/5443326233c5/ao4c05212_0010.jpg

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