Hyper-crosslinked porous ionic polymers (HCPIPs) have garnered significant attention due to their unique ionic properties and high specific surface areas. However, the limited variety of monomers, low ionic density, and difficulty in functionalization restrict their development. Herein, a series of functionalized non-cationic HCPIPs with high ionic density are designed and directly synthesized an innovative and straightforward approach - anion (and cation) hyper-crosslinking of tetraphenylborate-based ionic liquids (ILs). These HCPIPs offer controllable hydroxyl group content (0-2.40 mmol g), high IL content (1.20-1.78 mmol g), and large specific surface area (636-729 m g) with hierarchically ordered porous structures. These HCPIPs demonstrate exceptional CO adsorption capacities and CO/N adsorption selectivities, reaching up to 2.68-3.01 mmol g and 166-237, respectively, at 273 K and 1 bar. Furthermore, these ionic porous materials serve as highly efficient heterogeneous catalysts for CO cycloaddition to epoxides under mild conditions (1 bar CO, 60-80 °C, 12-24 h). Notably, the CO adsorption performances and catalytic activities of these HCPIPs are regulated by the hydroxyl groups within their structures, with enhancements observed as the number of hydroxyl groups increases. This work presents a facile and widely applicable method for constructing high-performance and task-specific HCPIPs.
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http://dx.doi.org/10.1039/d4sc03708a | DOI Listing |
Sci Rep
December 2024
Laboratorio de Fluidodinámica, Facultad de Ingeniería, Universidad de Buenos Aires/CONICET, Paseo Colón 850 CABA, Buenos Aires, Argentina.
The oil and gas industry faces two significant challenges, including rising global temperatures and depletion of reserves. Enhanced recovery techniques such as polymer flooding have positioned themselves as an alternative that attracts international attention thanks to increased recovery factors with low emissions. However, existing physical models need further refinement to improve predictive accuracy and prevent design failures in polymer flooding projects.
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December 2024
Department of Chemistry G. Ciamician, University of Bologna, Bologna, 40126, Italy.
Gold nanoparticles (AuNPs) and their biocompatible conjugates find wide use as transducers in (bio)sensors and as Nano-pharmaceutics. The study of the interaction between AuNPs and proteins in representative application media helps to better understand their intrinsic behaviors. A multi-environment, multi-parameter screening strategy is proposed based on asymmetric flow field flow fractionation (AF4)-multidetector.
View Article and Find Full Text PDFNat Commun
December 2024
Key Laboratory of Advanced Technologies of Materials (Ministry of Education), School of Materials Science and Engineering, Southwest Jiaotong University, Chengdu, 610031, China.
Piezoelectric electronics possess great potential in flexible sensing and energy harvesting applications. However, they suffer from low electromechanical performance in all-organic piezoelectric systems due to the disordered and weakly-polarized interfaces. Here, we demonstrated an all-polymer piezo-ionic-electric electronics with PVDF/Nafion/PVDF (polyvinylidene difluoride) sandwich structure and regularized ion-electron interfaces.
View Article and Find Full Text PDFJ Phys Chem B
December 2024
Department of Chemistry, The Pennsylvania State University, University Park, Pennsylvania 16802, United States.
The cloud point temperatures of aqueous poly(-isopropylacrylamide) (PNIPAM) and poly(ethylene) oxide (PEO) solutions were measured from pH 1.0 to pH 13.0 at a constant ionic strength of 100 mM.
View Article and Find Full Text PDFACS Appl Energy Mater
December 2024
Department of Chemical and Environmental Process Engineering, Faculty of Chemical Technology and Biotechnology, Budapest University of Technology and Economics, Műegyetem rkp. 3, Budapest H-1111, Hungary.
Amphiphilic copolymers of comb-like poly(poly(ethylene glycol) methacrylate) (PPEGMA) with methyl methacrylate (MMA) synthesized by one-pot atom transfer radical polymerization were mixed with lithium bis (trifluoromethanesulfonyl) imide salt to formulate dry solid polymer electrolytes (DSPE) for semisolid-state Li-ion battery applications. The PEO-type side chain length (EO monomer's number) in the PEGMA macromonomer units was varied, and its influence on the mechanical and electrochemical characteristics was investigated. It was found that the copolymers, due to the presence of PMMA segments, possess viscoelastic behavior and less change in mechanical properties than a PEO homopolymer with 100 kDa molecular weight in the investigated temperature range.
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