通过碎片再激活实现热固性材料的多代回收。

IF 15.6 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Journal of the American Chemical Society Pub Date : 2025-04-16 Epub Date: 2025-04-03 DOI:10.1021/jacs.4c17395
Kwangwook Ko, Edgar B Mejia, Hayden E Fowler, Suong T Nguyen, Yasmeen AlFaraj, Yuyan Wang, Samuel C Leguizamon, Nancy R Sottos, Jeremiah A Johnson
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引用次数: 0

摘要

热固性塑料因其出色的稳定性和机械性能而被广泛应用于工业领域;然而,其共价交联结构却限制了化学循环性。可裂解共聚单体(CC)提供了一种切实可行的策略,在不改变关键性能、成本或生产工作流程的情况下,为热固性塑料带来新的报废机会,例如可解构性或可重塑性。然而,迄今为止,CC 支持的热固性塑料回收仅限于一次循环,回收率为 25%。在这里,我们引入了一种 "片段再活化 "策略,即用功能基团活化从 CC 热固性塑料解构过程中获得的低聚物片段,从而提高片段的溶解性和反应性,以便进行后续循环。通过使用含有低含量硅氧烷基 CC 的工业烃类热固性材料聚双环戊二烯(pDCPD),我们首先展示了两轮化学循环,将上一代解构得到的 40 wt % 降冰片烯硅醚活化片段加入其中。然后,我们展示了解构和再活化这两个步骤可以统一为一个步骤,即 "解构再活化"。利用这种方法,我们展示了三轮化学回收,每轮回收 40-45 wt % 的碎片,同时保持关键材料的特性和可解构性。这三代再循环有效地延长了可解构 pDCPD 热固性材料的寿命 2.6 倍。结合 CCs,碎片再活化技术为提高热固性塑料的化学回收效率提供了一种前景广阔且具有潜在推广价值的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Multi-Generation Recycling of Thermosets Enabled by Fragment Reactivation.

Multi-Generation Recycling of Thermosets Enabled by Fragment Reactivation.

Thermosets are used in numerous industrial applications due to their excellent stabilities and mechanical properties; however, their covalently cross-linked structures limit chemical circularity. Cleavable comonomers (CCs) offer a practical strategy to impart new end-of-life opportunities, such as deconstructability or remoldability, to thermosets without altering critical properties, cost, or manufacturing workflows. Nevertheless, CC-enabled recycling of thermosets has so far been limited to one cycle with a 25% recycled content. Here, we introduce a "fragment reactivation" strategy, wherein the oligomeric fragments obtained from CC-enabled thermoset deconstruction are activated with functional groups that improve fragment solubility and reactivity for subsequent rounds of recycling. Using polydicyclopentadiene (pDCPD), an industrial hydrocarbon thermoset material, containing low loadings of a siloxane-based CC, we first demonstrate two rounds of chemical recycling by incorporating 40 wt % norbornene silyl ether-reactivated fragments derived from the prior generation's deconstruction. Then, we show that the two-step sequence of deconstruction and reactivation can be unified into a single-step process, referred to as "deconstructive reactivation." Using this approach, we demonstrate three rounds of chemical recycling with 40-45 wt % fragments incorporated per cycle while maintaining key material properties and deconstructability. These three generations of recycling effectively extend the lifespan of deconstructable pDCPD thermosets by ∼2.6 times. Combined with CCs, fragment reactivation presents a promising and potentially generalizable strategy to improve the chemical recycling efficiency of thermosets.

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来源期刊
CiteScore
24.40
自引率
6.00%
发文量
2398
审稿时长
1.6 months
期刊介绍: The flagship journal of the American Chemical Society, known as the Journal of the American Chemical Society (JACS), has been a prestigious publication since its establishment in 1879. It holds a preeminent position in the field of chemistry and related interdisciplinary sciences. JACS is committed to disseminating cutting-edge research papers, covering a wide range of topics, and encompasses approximately 19,000 pages of Articles, Communications, and Perspectives annually. With a weekly publication frequency, JACS plays a vital role in advancing the field of chemistry by providing essential research.
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