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Catalyst Influence on Undesired Side Reactions in the Polycondensation of Fully Bio-Based Polyester Itaconates

机译:完全生物基聚酯衣康酸酯缩聚反应中催化剂对不希望有的副反应的影响

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摘要

Bio-based unsaturated polyester resins derived from itaconic acid can be an alternative to established resins of this type in the field of radical-curing resins. However, one of the challenges of these polyester itaconates is the somewhat more elaborate synthetic process, especially under polycondensation conditions used on an industrial scale. The α,β-unsaturated double bond of the itaconic acid is prone to side reactions that can lead to the gelation of the polyester resin under standard conditions. This is especially true when bio-based diols such as 1,3-propanediol or 1,4-butanediol are used to obtain resins that are 100% derived from renewable resources. It was observed in earlier studies that high amounts of these aliphatic diols in the polyester lead to low conversion and gelation of the resins. In this work, a catalytic study using different diols was performed in order to elucidate the reasons for this behavior. It was shown that the choice of catalyst has a crucial influence on the side reactions occurring during the polycondensation reactions. In addition, the side reactions taking place were identified and suppressed. These results will allow for the synthesis of polyester itaconates on a larger scale, setting the stage for their industrial application.
机译:在自由基固化树脂领域,衍生自衣康酸的生物基不饱和聚酯树脂可以替代这种类型的已建立树脂。然而,这些聚酯衣康酸酯的挑战之一是合成过程有些复杂,特别是在工业规模使用的缩聚条件下。衣康酸的α,β-不饱和双键易于发生副反应,在标准条件下会导致聚酯树脂胶凝。当使用生物基二醇(例如1,3-丙二醇或1,4-丁二醇)来获得100%源自可再生资源的树脂时,尤其如此。在较早的研究中观察到,聚酯中大量的这些脂肪族二醇导致树脂的低转化率和凝胶化。在这项工作中,进行了使用不同二醇的催化研究,以阐明这种行为的原因。结果表明,催化剂的选择对缩聚反应期间发生的副反应有至关重要的影响。另外,识别并抑制了发生的副反应。这些结果将允许大规模合成聚酯衣康酸酯,为其工业应用奠定基础。

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