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从具有三环氢化菲骨架的脱氢枞酸到生物基超分子水凝胶的简便构建及稳定的凝胶乳液。

Facile Construction of Bio-Based Supramolecular Hydrogels from Dehydroabietic Acid with a Tricyclic Hydrophenanthrene Skeleton and Stabilized Gel Emulsions.

机构信息

College of Chemical Engineering, Huaqiao University, Xiamen 361021, China.

出版信息

Molecules. 2021 Oct 28;26(21):6526. doi: 10.3390/molecules26216526.

DOI:10.3390/molecules26216526
PMID:34770933
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8586928/
Abstract

Supramolecular hydrogels have attracted great attention due to their special properties. In this research, bio-based supramolecular hydrogels were conveniently constructed by heating and ultrasounding two components of dehydroabietic acid with a rigid tricyclic hydrophenanthrene skeleton and morpholine. The microstructures and properties of hydrogels were investigated by DSC, rheology, SAXS, CD spectroscopy, and cryo-TEM, respectively. The critical gel concentration (CGC) of the hydrogel was 0.3 mol·L and the gel temperature was 115 °C. In addition, the hydrogel showed good stability and mechanical properties according to rheology results. Cryo-TEM images reveal that the microstructure of hydrogel is fibrous meshes; its corresponding mechanism has been studied using FT-IR spectra. Additionally, oil-in-water gel emulsions were prepared by the hydrogel at a concentration above its CGC, and the oil mass fraction of the oil-in-water gel emulsions could be freely adjusted between 5% and 70%. This work provides a convenient way to prepare bio-based supramolecular hydrogels and provides a new method for the application of rosin.

摘要

由于具有特殊性质,超分子水凝胶引起了广泛关注。在这项研究中,通过加热和超声两种成分(具有刚性三环氢化菲骨架和吗啉的脱氢枞酸),方便地构建了基于生物的超分子水凝胶。通过 DSC、流变学、小角 X 射线散射、圆二色光谱和冷冻透射电镜分别研究了水凝胶的微观结构和性能。水凝胶的临界凝胶浓度(CGC)为 0.3 mol·L,凝胶温度为 115°C。此外,根据流变学结果,水凝胶显示出良好的稳定性和机械性能。冷冻透射电镜图像显示水凝胶的微观结构为纤维状网格;使用傅里叶变换红外光谱研究了其相应的形成机制。此外,在水凝胶浓度高于其 CGC 时可以制备油包水乳状液,油包水乳状液的油质量分数可以在 5%至 70%之间自由调节。这项工作为制备基于生物的超分子水凝胶提供了一种简便的方法,并为松香的应用提供了一种新方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9aa/8586928/ac72d77b193c/molecules-26-06526-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9aa/8586928/e569ad9000e8/molecules-26-06526-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9aa/8586928/585281a50ff0/molecules-26-06526-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9aa/8586928/aac930a94aa6/molecules-26-06526-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9aa/8586928/e7aa17b1f777/molecules-26-06526-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9aa/8586928/b8b2ce3d8a1e/molecules-26-06526-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9aa/8586928/85ff88db6357/molecules-26-06526-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9aa/8586928/ef02144401de/molecules-26-06526-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9aa/8586928/640f23d34542/molecules-26-06526-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9aa/8586928/ac72d77b193c/molecules-26-06526-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9aa/8586928/e569ad9000e8/molecules-26-06526-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9aa/8586928/585281a50ff0/molecules-26-06526-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9aa/8586928/aac930a94aa6/molecules-26-06526-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9aa/8586928/e7aa17b1f777/molecules-26-06526-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9aa/8586928/b8b2ce3d8a1e/molecules-26-06526-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9aa/8586928/85ff88db6357/molecules-26-06526-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9aa/8586928/ef02144401de/molecules-26-06526-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9aa/8586928/640f23d34542/molecules-26-06526-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9aa/8586928/ac72d77b193c/molecules-26-06526-sch001.jpg

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