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Polyurethane ranks as one of the most significant plastics globally in terms of production volume and economic value, serving a crucial role in modern society. Due to complexities in the chemical recycling of polyurethane, replacement rates in recycled materials tend to be low, and the recovery of the isocyanate-derived aromatic compounds is often neglected. While many recycling efforts try to address these shortcomings, they primarily focus on TDI-based flexible foams, as recycling rigid PU foams is more challenging. In this work, ammonolysis is reported as an effective method for the recycling of rigid PU foams using ammonia to efficiently produce aromatic amines and polyols, while enabling easy recovery of the excess ammonia. A quantitative H NMR analysis method was developed for rigid PU materials, allowing for the identification and quantification of the polyol and isocyanate-derived products of rigid PU. For ammonolysis, volumetric productivities of up to 300 g·L·h were obtained, surpassing current rigid PU recycling processes and highlighting its industrial significance. Kinetic studies provided mechanistic insight into PU depolymerization, with urea linkages splitting fastest, followed by carbamates and finally isocyanurates. Furthermore, solid-state NMR analysis demonstrated ammonia's hydrogen bonds disrupting effect in PU hard segments, presenting ammonolysis as an optimal method for recycling rigid PU foams, where the high content of hard segments makes degradation more challenging. The ammonolysis mixture could be purified into pure polyol and aromatic amine product fractions using two different separation methods. Finally, to highlight its industrial potential, our ammonolysis approach was demonstrated on various PU materials, extending the scope to end-of-life rigid PU waste materials. A comprehensive recycling process was applied, surpassing current rigid PU recycling efforts by reaching high isolated yields for isocyanate derivatives and polyol.
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http://dx.doi.org/10.1021/jacsau.5c00496 | DOI Listing |
Adv Mater
September 2025
Department of Mechanical Engineering, University of Alberta, Edmonton, AB, T6G 1H9, Canada.
Polyesters, with their tunable chemical structures and environmental sustainability, have drawn growing attention as solid polymer electrolytes for next-generation solid-state lithium metal batteries (SSLMBs). Through a comprehensive experimental and theoretical study involving the systematic variation of carbon chain lengths in the flexible (diol) and coordinating (diacid) segments, along with selective fluorination at distinct positions along the polymer backbone, 18 types of polyester are fabricated and demonstrate that fluorination at the coordinating segment significantly enhances ionic conductivity by suppressing crystallinity. In contrast, fluorination at the flexible segment reduces ionic migration barriers by providing more homogeneous coordinating sites, thereby improving the lithium-ion transference number, despite increasing chain rigidity and a reduction in overall ionic conductivity.
View Article and Find Full Text PDFInt J Biol Macromol
September 2025
Key Lab of Rubber-Plastics, Ministry of Education/Shandong Provincial Key, Lab of Rubber-Plastics, School of Polymer Science and Engineering, Qingdao University of Science and Technology, Qingdao, 266042, China. Electronic address:
A dynamically crosslinked network VEC (vulcanized ESO and CA) was synthesized in situ via zinc acetate-catalyzed epoxy ring-opening between epoxidized soybean oil (ESO) and anhydrous citric acid (CA), then incorporated into polylactic acid (PLA)/polybutylene adipate terephthalate (PBAT) blends to enhance interfacial compatibility. The dynamic ester-exchange network acted as an intermediate phase, improving the integration of the flexible PBAT phase within the rigid PLA matrix. VEC content critically influenced mechanical properties, with in-situ crosslinking during dynamic vulcanization enhancing chain interactions and blend homogeneity.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2025
School of Chemistry and Chemical Engineering, Anhui University of Technology, Ma'anshan, 243000, China.
The photocatalytic efficiency of two-dimensional covalent organic frameworks (2D COFs) is governed by the spatial arrangement of donor-acceptor (D-A) moieties, which strongly influences exciton transport. However, precise control over D-A alignment, especially across intra- and interlayer dimensions, remains a key challenge for optimizing singlet oxygen (O) generation. Here, we present a linker geometry-directed approach to modulate D-A organization within perylene diimide (PDI)-based COFs.
View Article and Find Full Text PDFPolymers (Basel)
August 2025
Department of Mechanical and Manufacturing Engineering, University of Cyprus, 2109 Nicosia, Cyprus.
The increasing demand for sustainable construction materials has driven research into the reuse of plastic waste for renewable building applications. This study introduces a new lightweight insulating mortar for floor and roof systems, utilizing recycled rigid polyurethane (PU) foam as the primary aggregate. The binder mainly consists of Portland cement, with no added sand, and includes minor additives to enhance mechanical, physical, and thermal properties.
View Article and Find Full Text PDFMaterials (Basel)
August 2025
Key Laboratory of Bio-based Material Science & Technology, Northeast Forestry University, Ministry of Education, 26 Hexing Road, Harbin 150040, China.
In this study, alkali-treated wood flour/dynamic polyurethane composites were successfully prepared through a solvent-free one-pot method and in situ polymerization. The effects of the alkaline treatment process, changes in the flexible long-chain content in the dynamic polyurethane system, and the wood flour filling amount on the interface's bonding, mechanical, and reprocessing properties were investigated. Partial removal of lignin and hemicellulose from the alkali-treated wood flour enhanced rigidity and improved interface bonding and mechanical strength when combined with dynamic polyurethane.
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