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1.
Science ; 385(6711): 854-860, 2024 Aug 23.
Artigo em Inglês | MEDLINE | ID: mdl-39172828

RESUMO

Wind energy is helping to decarbonize the electrical grid, but wind blades are not recyclable, and current end-of-life management strategies are not sustainable. To address the material recyclability challenges in sustainable energy infrastructure, we introduce scalable biomass-derivable polyester covalent adaptable networks and corresponding fiber-reinforced composites for recyclable wind blade fabrication. Through experimental and computational studies, including vacuum-assisted resin-transfer molding of a 9-meter wind blade prototype, we demonstrate drop-in technological readiness of this material with existing manufacture techniques, superior properties relative to incumbent materials, and practical end-of-life chemical recyclability. Most notable is the counterintuitive creep suppression, outperforming industry state-of-the-art thermosets despite the dynamic cross-link topology. Overall, this report details the many facets of wind blade manufacture, encompassing chemistry, engineering, safety, mechanical analyses, weathering, and chemical recyclability, enabling a realistic path toward biomass-derivable, recyclable wind blades.

2.
JACS Au ; 1(9): 1342-1347, 2021 Sep 27.
Artigo em Inglês | MEDLINE | ID: mdl-34604843

RESUMO

Synthetic aromatic polymers are ubiquitous and indispensable to modern life, industry, and the global economy. The direct functionalization of these materials remains a considerable challenge on account of their unreactive aromatic C-H bonds and robust physical properties. Here, we demonstrate that homogeneous gold catalysis offers a mild, chemoselective, and practical approach to functionalize high-volume commodity aromatic polymers. Utilizing a gold-catalyzed intermolecular hydroarylation between a methyl ester functionalized alkyne, methyl propiolate, and nucleophilic arenes within polystyrene (PS) results in direct functionalization of phenyl rings with 1,2-substituted methyl acrylate functional groups. The reactivity and functionalization depend on the steric and electronic environment of the catalyst, counterion pairing, and method of activation. The reactivity is broad in scope, enabling the functionalization of arenes within commercial polysulfone (PSU) and waste polyethylene terephthalate (PET). These reactions open new opportunities to chemically transform aromatic polymers and modify their physical properties.

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