Liquid Metal Nanoparticles Physically Hybridized with Cellulose Nanocrystals Initiate and Toughen Hydrogels with Piezoionic Properties

Liquid metal (LM) particles can serve as initiators, functional fillers, and cross-linkers for hydrogels. Herein, we show that cellulose nanocrystals (CNCs) stabilize LM particles in aqueous solutions, such as those used to produce hydrogels. The CNC-coated LM particles initiate free-radical polymerization to form poly­(acrylic acid) (PAA) hydrogel with exceptional propertiesstretchability ∼2000%, excellent toughness ∼1.8 MJ/m3, mechanical resilience, and efficient self-healingrelative to cross-linked PAA networks polymerized using conventional molecular initiators. FTIR spectroscopy, rheology, and mechanical measurements suggest that physical bonds between PAA and both Ga3+ and LM-CNC particles contribute to the excellent mechanical properties. The gels are used to sense a wide range of strains, such as those associated with human motion, via changes in resistance through the gel. The sensitivity at low strains enables monitoring subtle physiological signals, such as pulse. Without significantly compromising the toughness, soaking the gels in salt solution brings about high ionic conductivity (3.8 S/m), enabling them to detect touch via piezoionic principles; the anions in the gel have higher mobility than cations, resulting in significant charge separation (current ∼30 μA, ∼10 μA/cm2) through the gel in response to touch. These attractive properties are promising for wearable sensors, energy harvesters, and self-powered ionic touch panels

Solubility, Diffusivity, and Permeability of HFC-32 and HFC-125 in Amorphous Copolymers of Perfluoro(butenyl vinyl ether) and Perfluoro(2,2-dimethyl-1,3-dioxole)

R-410A, an azeotropic mixture composed of 50 wt % difluoromethane (HFC-32, CH2F2) and 50 wt % pentafluoroethane (HFC-125, CHF2CF3) used in residential and commercial air-conditioning applications, will be phased down due to the high global warming potential (GWP) of HFC-125. The HFC-32 can be reused in low-GWP blends containing hydrofluoroolefins (HFOs); however, incumbent separation technology, fractional distillation, cannot separate azeotropic mixtures. Membrane technology provides the opportunity to achieve a selective separation of azeotropic HFC refrigerant mixtures with lower energy consumption and capital requirements. This study explores the use of amorphous perfluoropolymers for the separation of R-410A. The permeability, solubility, and diffusivity of HFC-32 and HFC-125 were measured in copolymers of perfluoro(butenyl vinyl ether) (PBVE) and perfluoro(2,2-dimethyl-1,3-dioxole) (PDD). Pure gas permeability of HFC-32 and HFC-125 were measured using a static membrane apparatus and the pressure-rise method. Solubility measurements were obtained using a gravimetric microbalance, and diffusivity was calculated using a Fickian model. The results indicate that a high permeability and selectivity of HFC-32/HFC-125 can be obtained with a 50 wt % PBVE and 50 wt % PDD copolymer and that the separation is diffusion-driven over the entire range of compositions tested