Univ. Lille, CNRS, Centrale Lille, Univ. Artois, UMR 8181 - UCCS - Unité De Catalyse Et Chimie Du Solide, F-59000, Lille, France.
Roquette Frères, F-62080, Lestrem Cedex, France.
Carbohydr Polym. 2021 Feb 15;254:117399. doi: 10.1016/j.carbpol.2020.117399. Epub 2020 Nov 13.
Starch based materials are attractive bio-based alternative to fully synthetic polymers. Native starch has however limited thermoprocessability and properties and must be modified. In order to improve the properties of starch-graft-poly(butyl-acrylate-co-styrene) copolymers via a process as green as possible, we report herein a new method for the dual functionalization of the polysaccharide via a one pot one step reaction in aqueous medium combining free radical polymerizations and ring-opening chemistry. Poly(butyl acrylate) or poly(butyl acrylate-co-styrene) (ca. 60 000 g/mol) and oligo(ε-caprolactone) were grafted on starch with a grafting percentage up to 75 %. The copolymers show two glass transition temperatures: one around 55-60 °C related to starch and a second attributed to the grafted vinyl polymers, from -46 °C to 20 °C depending on butyl acrylate/styrene ratio. The resulting dual functionalized materials exhibit excellent mechanical properties, with elongation at break in the range 20-210 %, while single functionalized starch shows less than 5 %.
淀粉基材料是一种有吸引力的生物基全合成聚合物替代品。然而,天然淀粉的热加工性能和性能有限,必须进行改性。为了通过尽可能绿色的工艺来提高淀粉接枝-聚(丁基丙烯酸酯-共-苯乙烯)共聚物的性能,我们在此报告了一种通过一锅一步反应在水介质中对多糖进行双重官能化的新方法,该反应结合了自由基聚合和开环化学。聚(丁基丙烯酸酯)或聚(丁基丙烯酸酯-共-苯乙烯)(约 60000 g/mol)和低聚(ε-己内酯)接枝到淀粉上,接枝率高达 75%。共聚物显示出两个玻璃化转变温度:一个在 55-60°C 左右与淀粉有关,另一个归因于接枝的乙烯基聚合物,取决于丁基丙烯酸酯/苯乙烯的比例,从-46°C 到 20°C。所得的双重官能化材料表现出优异的机械性能,断裂伸长率在 20-210%范围内,而单一官能化的淀粉则小于 5%。