The improved low?field electro?actuation of dielectric elastomer composites regulated by entirely?inorganic BaTiO3@TiO2 core?shell construction

Multi?ionic block copolymers with sulfonated amines and counter?ion substitution selectively allow the permeation of water, while inhibiting the transport of chemicals.AbstractThis study discusses the synthesis of sulfonated amine block copolymers and the effect of multiple ionic domains and counter?ion substitution on polymeric membranes' morphology and transport properties for chemical protective clothing (CPC) applications. The monomers 2?(tert?butylamino) ethyl methacrylate, 2?ethoxy ethyl methacrylate, and styrene were used to prepare the block copolymers by atom transfer radical polymerization (ATRP). The copolymers were then sulfonated by chemical grafting with pendants sulfobutyl groups onto the polymer structure. Properties of the resulting membranes were evaluated as a function of block composition, incorporation of sulfonic groups, and counter?ion substitution. Blended membranes with sulfonated poly(styrene?isobutylene?styrene) (SIBS) were also studied. A series of materials characterization techniques (e.g., Fourier?transform infrared spectroscopy [FT?IR], thermogravimetric analysis [TGA], atomic force microscopy [AFM], Small?angle X?ray scattering [SAXS]/wide?angle X?ray scattering [WAXS]) were performed to describe the changes to the membranes. The results indicate that synthesized copolymers lack phase segregation mainly because of a low sulfonation on the central amine block, leading the material to have a low Water/DMMP selectivity. As the sulfonated copolymers were blended with SIBS 75, the breathability of the membranes were enhanced 1.5 times, and almost all candidates achieved the water vapor transport rate limit of 1500?g?m?2 day?1. Finally, the better?found candidates for DMMP CPC were Mg2+ membranes, achieving selectivity between 20 and 90 range.

» Publication Date: 04/01/2023

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This project has received funding from the European Union's Horizon 2020 research and innovation programme under grant agreement Nº 768737


                   




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