源自萜类丙烯酸酯的聚(HIPE

IF 2.2 4区 化学 Q3 CHEMISTRY, PHYSICAL
Stanko Kramer, Nastja Slavič, Peter Krajnc
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引用次数: 0

摘要

利用非化石燃料来源生产聚合物的需求日益增长。在本研究中,使用丙烯酰氯通过酯化程序修饰了萜类化合物四氢大麻酚、香茅醇和壬泊酚,形成了萜类丙烯酸酯。合成的丙烯酸酯被用于通过高内相乳液(HIPE)模板生产分层多孔聚合物,乳液由体积分数为 85% 的有机相(单体)和水相组成。有机相中的丙烯酸酯萜类与三羟甲基丙烷三丙烯酸酯(TMPTA)交联形成聚 HIPE。为了研究聚 HIPE 生产的可行性,交联度分别为 5 摩尔%和 10 摩尔%。虽然两种交联度都能合成聚合物,但只有 10 mol% 的交联度才能产生典型的相互连接的多孔细胞拓扑结构。丙烯酸四氢geraniol酯和丙烯酸香茅酯的平均主孔直径分别为 15.6 微米和 16.5 微米,而丙烯酸nopol酯的平均主孔直径为 5.6 微米。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Poly(HIPEs) from terpenoid-derived acrylates

Poly(HIPEs) from terpenoid-derived acrylates

The need for utilization of non-fossil fuel derived sources for polymer production is growing. In this study the terpenoids tetrahydrogeraniol, citronellol and nopol were modified with an esterification procedure using acryloyl chloride, forming terpenoid acrylates. The synthesised acrylates were used for the production of hierarchically porous polymers via high internal phase emulsion (HIPE) templating with emulsions consisting of an organic (monomer) phase and an aqueous phase with a volume fraction of 85%. The acrylate terpenoids in the organic phase were crosslinked with trimethylolpropane triacrylate (TMPTA) to form the polyHIPEs. A crosslinking degree of 5 and 10 mol% was used to investigate the feasibility of polyHIPE production. While both crosslinking degrees enabled the synthesis of polymers, only the 10 mol% crosslinking yielded the typical interconnected porous cellular topology. The average primary pore diameter in the case of the tetrahydrogeraniol acrylate and citronellyl acrylate was 15.6 and 16.5 μm, respectively, while the average primary pore diameter in the case of nopol acrylate was 5.6 μm.

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来源期刊
Colloid and Polymer Science
Colloid and Polymer Science 化学-高分子科学
CiteScore
4.60
自引率
4.20%
发文量
111
审稿时长
2.2 months
期刊介绍: Colloid and Polymer Science - a leading international journal of longstanding tradition - is devoted to colloid and polymer science and its interdisciplinary interactions. As such, it responds to a demand which has lost none of its actuality as revealed in the trends of contemporary materials science.
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