Bourguignon Maxime, Grignard Bruno, Detrembleur Christophe
Center for Education and Research on Macromolecules (CERM), CESAM Research Unit, University of Liege, Sart-Tilman B6a, Liege 4000, Belgium.
FRITCO2T Platform, University of Liege, Sart-Tilman B6a, Liege 4000, Belgium.
J Am Chem Soc. 2024 Jan 10;146(1):988-1000. doi: 10.1021/jacs.3c11637. Epub 2023 Dec 29.
For decades, self-blown polyurethane foams─found in an impressive range of materials─are produced by the toxic isocyanate chemistry and are difficult to recycle. Producing them in existing production plants by a rapid isocyanate-free self-blowing process from room temperature (RT) formulations is a long-lasting challenge. The recent water-induced self-blowing of nonisocyanate polyurethane (NIPU) formulations composed of a CO-based tricyclic carbonate, diamine, water, and a catalyst successfully addressed the isocyanate issue, however failed to provide foams at RT. Herein, we elaborate a practical solution to empower the NIPU foam formation in record timeframes from RT formulations. We generate cascade exotherms by the addition of a highly reactive triamine and an epoxide to the formulation of the water-induced self-foaming process. These exotherms, combined to a fast cross-linking imparted by the triamine and epoxide, rapidly raise the temperature to the foaming threshold and deliver hybrid NIPU foams in 5 min with KOH as a catalyst. Careful selection of the monomers enables producing foams with a wide range of properties, as well as with an unprecedented high biobased content up to 90 wt %. Moreover, foams can be upcycled into polymer films by hot pressing, offering them a facile reuse scenario. This robust cheap process opens huge perspectives for greener foams of high biobased contents, expectedly responding to the sustainability demands of the foam sector. It is potentially compatible to the retrofitting of industrial foaming infrastructures, which is of paramount importance to accommodate existing foam production plants and address the huge foam market demands.
几十年来,自发泡聚氨酯泡沫材料存在于一系列令人印象深刻的材料中,由有毒的异氰酸酯化学工艺生产,且难以回收利用。在现有生产工厂中,通过快速无异氰酸酯自发泡工艺,从室温配方生产这些材料一直是一项长期挑战。最近,由基于CO的三环碳酸酯、二胺、水和催化剂组成的非异氰酸酯聚氨酯(NIPU)配方通过水引发自发泡成功解决了异氰酸酯问题,但未能在室温下提供泡沫材料。在此,我们阐述了一种切实可行的解决方案,能够在创纪录的时间内从室温配方实现NIPU泡沫材料的形成。我们通过向水引发自发泡工艺的配方中添加高活性三胺和环氧化物来产生级联放热反应。这些放热反应与三胺和环氧化物赋予的快速交联相结合,迅速将温度升高至发泡阈值,并在以KOH为催化剂的情况下5分钟内制成混合NIPU泡沫材料。仔细选择单体能够生产具有广泛性能的泡沫材料,以及具有高达90 wt%的前所未有的高生物基含量的泡沫材料。此外,泡沫材料可以通过热压升级为聚合物薄膜,为它们提供了一种简便的再利用方案。这种强大且廉价的工艺为具有高生物基含量的更环保泡沫材料开辟了广阔前景,有望满足泡沫材料行业的可持续发展需求。它有可能与工业发泡基础设施的改造兼容,这对于适应现有的泡沫材料生产工厂和满足巨大的泡沫材料市场需求至关重要。