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由各种生物衍生平台分子合成不饱和聚酯树脂。

Synthesis of Unsaturated Polyester Resins from Various Bio-Derived Platform Molecules.

作者信息

Farmer Thomas J, Castle Rachael L, Clark James H, Macquarrie Duncan J

机构信息

Green Chemistry Centre of Excellence, Department of Chemistry, University of York, Heslington, York YO10 5DD, UK.

出版信息

Int J Mol Sci. 2015 Jul 2;16(7):14912-32. doi: 10.3390/ijms160714912.

Abstract

Utilisation of bio-derived platform molecules in polymer synthesis has advantages which are, broadly, twofold; to digress from crude oil dependence of the polymer industry and secondly to reduce the environmental impact of the polymer synthesis through the inherent functionality of the bio-derived platform molecules. Bulk polymerisation of bio-derived unsaturated di-acids has been employed to produce unsaturated polyester (UPEs) which have been analysed by GPC, TGA, DSC and NMR spectroscopy, advancing on the analysis previously reported. UPEs from the diesters of itaconic, succinic, and fumaric acids were successfully synthesised with various diols and polyols to afford resins of MN 480-477,000 and Tg of -30.1 to -16.6 °C with solubilities differing based on starting monomers. This range of properties allows for many applications and importantly due to the surviving Michael acceptor moieties, solubility and cross-linking can be specifically tailored, post polymerisation, to the desired function. An improved synthesis of itaconate and succinate co-polymers, via the initial formation of an itaconate bis-diol, is also demonstrated for the first time, resulting in significantly improved itaconate incorporation.

摘要

在聚合物合成中利用生物衍生的平台分子具有广泛的双重优势;一是摆脱聚合物行业对原油的依赖,二是通过生物衍生平台分子的固有功能降低聚合物合成对环境的影响。已采用生物衍生的不饱和二酸的本体聚合来生产不饱和聚酯(UPEs),并通过凝胶渗透色谱法(GPC)、热重分析法(TGA)、差示扫描量热法(DSC)和核磁共振光谱法(NMR)对其进行了分析,这是在先前报道的分析基础上的进一步发展。成功地用各种二醇和多元醇合成了衣康酸、琥珀酸和富马酸二酯的UPEs,得到了数均分子量(MN)为480 - 477,000且玻璃化转变温度(Tg)为-30.1至-16.6℃的树脂,其溶解度因起始单体而异。这种性能范围允许许多应用,重要的是由于残留的迈克尔受体部分,聚合后可以根据所需功能对溶解度和交联进行特定调整。首次还展示了通过最初形成衣康酸双二醇来改进衣康酸酯和琥珀酸酯共聚物的合成方法,从而显著提高了衣康酸酯的掺入量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a76b/4519879/3a78447da618/ijms-16-14912-g008.jpg

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