The development of chemically recyclable polymers with desirable properties is a long-standing but challenging goal in polymer science. Central to this challenge is the need for reversible chemical reactions that can equilibrate at rapid rates and provide efficient polymerization and depolymerization cycles. Based on the dynamic chemistry of nucleophilic aromatic substitution (SAr), we report a chemically recyclable polythioether system derived from readily accessible benzothiocane () monomers. This system represents the first example of a well-defined monomer platform capable of chain-growth ring-opening polymerization through an SAr manifold. The polymerizations reach completion in minutes, and the pendant functionalities are easily customized to tune material properties or render the polymers amenable to further functionalization. The resulting polythioether materials exhibit comparable performance to commercial thermoplastics and can be depolymerized to the original monomers in high yields.
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http://dx.doi.org/10.1021/jacs.3c03455 | DOI Listing |
Sci Rep
December 2024
Faculty of Mechanical Engineering, Department of Machining, Assembly and Engineering Metrology, VSB-Technical University of Ostrava, Ostrava-Poruba, 708 00, Czech Republic.
The aim of this work is to investigate the sound absorption properties of open-porous polyamide 12 (PA12) structures produced using Selective Laser Sintering (SLS) technology. The examined 3D-printed samples, fabricated with hexagonal prism lattice structures, featured varying thicknesses, cell sizes, and orientations. Additionally, some samples were produced with an outer shell to evaluate its impact on sound absorption.
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December 2024
Department of Organic Chemistry, Faculty of Chemistry, University of Mazandaran, Babolsar, Iran.
Polymer-based catalysts have garnered significant interest for their efficiency, reusability, and compatibility with various synthesis processes. In catalytic applications, polymers offer the advantage of structural versatility, enabling functional groups to be tailored for specific catalytic activities. In this study, we developed a novel magnetic copolymer of methyl methacrylate and maleic anhydride (PMMAn), synthesized via in situ chemical polymerization of methyl methacrylate onto maleic anhydride, using benzoyl peroxide as a free-radical initiator.
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December 2024
Department of Organic and Polymer Chemistry, Faculty of Chemistry, Kharazmi University, Tehran, 15719-14911, Iran.
This study investigates the repurposing of asphaltene, a petroleum waste product, as a catalyst for organic reactions. Sulfonated asphaltene was synthesized and evaluated for its efficacy in catalyzing the Mannich reaction, displaying notable diastereoselectivity and operating effectively under mild conditions. Characterization of the catalyst's chemical composition, structure, and thermal stability was conducted using FT-IR, TGA, XRD, CHN, BET-BJH, SEM, and EDS analyses.
View Article and Find Full Text PDFInt J Biol Macromol
December 2024
School of Chemical Engineering, Changchun University of Technology, Changchun 130012, China.
In this study, we developed a novel composite catalytic hydrogel, which integrates excellent mechanical properties, catalytic activity, and sensing performance. Discarded hydrogel sensors are reused as templates for in-situ generation of metal nanoparticles, and multifunctional hydrogels combining sensing and catalysis are realized. Polyacrylamide (PAM) provides a three-dimensional network structure, while octadecyl methacrylate (SMA) acts as a hydrophobic association center, enhancing the structural stability of the hydrogel.
View Article and Find Full Text PDFPLoS One
December 2024
Department of Biological Sciences, Michigan Technological University, Houghton, Michigan, United States of America.
Millions of tons of polyethylene terephthalate (PET) are produced each year, however only ~30% of PET is currently recycled in the United States. Improvement of PET recycling and upcycling practices is an area of ongoing research. One method for PET upcycling is chemical depolymerization (through hydrolysis or aminolysis) into aromatic monomers and subsequent biodegradation.
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