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通过酶促聚合制备的高度支化生物基不饱和聚酯

Highly Branched Bio-Based Unsaturated Polyesters by Enzymatic Polymerization.

作者信息

Nguyen Hiep Dinh, Löf David, Hvilsted Søren, Daugaard Anders Egede

机构信息

Danish Polymer Centre, Department of Chemical and Biochemical Engineering, Technical University of Denmark, DK-2800 Kgs. Lyngby, Denmark.

Hempel A/S, Lundtoftegårdsvej 91, DK-2800 Kgs. Lyngby, Denmark.

出版信息

Polymers (Basel). 2016 Oct 14;8(10):363. doi: 10.3390/polym8100363.

Abstract

A one-pot, enzyme-catalyzed bulk polymerization method for direct production of highly branched polyesters has been developed as an alternative to currently used industrial procedures. Bio-based feed components in the form of glycerol, pentaerythritol, azelaic acid, and tall oil fatty acid (TOFA) were polymerized using an immobilized lipase B (CALB) and the potential for an enzymatic synthesis of alkyds was investigated. The developed method enables the use of both glycerol and also pentaerythritol (for the first time) as the alcohol source and was found to be very robust. This allows simple variations in the molar mass and structure of the polyester without premature gelation, thus enabling easy tailoring of the branched polyester structure. The postpolymerization crosslinking of the polyesters illustrates their potential as binders in alkyds. The formed films had good UV stability, very high water contact angles of up to 141° and a glass transition temperature that could be controlled through the feed composition.

摘要

一种用于直接生产高度支化聚酯的一锅法酶催化本体聚合方法已被开发出来,作为目前工业生产方法的替代方案。以甘油、季戊四醇、壬二酸和妥尔油脂肪酸(TOFA)形式存在的生物基进料组分,使用固定化脂肪酶B(CALB)进行聚合,并研究了醇酸树脂酶促合成的可能性。所开发的方法能够同时使用甘油和季戊四醇(首次)作为醇源,并且发现该方法非常稳定。这使得聚酯的摩尔质量和结构能够简单变化而不会过早凝胶化,从而能够轻松定制支化聚酯结构。聚酯的后聚合交联说明了它们作为醇酸树脂中粘合剂的潜力。形成的薄膜具有良好的紫外线稳定性、高达141°的非常高的水接触角以及可通过进料组成控制的玻璃化转变温度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d15b/6432132/89c00e6e5849/polymers-08-00363-sch001.jpg

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