Fabrication and excellent electroresponsive properties of ideal PMMA@BaTiO3 composite particles.

A series of core-shell-structured poly(methylmethacrylate)@BaTiO3 (PMMA@BT) composite particles were constructed via the self-assembly of BT nanoparticles on the surfaces of PMMA cores through the covalent bonding of siloxane groups at room temperature. The PMMA@BT composite particles were characterized by scanning electron microscopy, transmission electron microscopy, infrared spectroscopy, X-ray diffraction, video-based optical contact angle measurement, thermogravimetric analysis, and impedance analysis. The electroresponses of the obtained PMMA@BT composite particles were all stronger than that of pure BT, and the electroresponse depended on the weight percentage of the BT shell. The PMMA@BT particles with the optimal core-shell structure contained 58.14 wt% of BT shell. The surface hydrophilicity of the optimal particles was close to that of pure BT, and the dielectric constant was the greatest among the series of synthesized PMMA@BT particles. Thus, the optimized PMMA@BT particles demonstrated the strongest electroresponsive behavior in gelatin hydrogel elastomer, as demonstrated by polarized microscopy and dynamic mechanical analysis. The excellent electroresponsive property of the optimal PMMA@BT particles is reflected by the large sensitivity of the increase in storage modulus for the gelatin hydrogel elastomer containing the composite particles (21% at E = 0.8 kV mm-1 and a particle loading of 1.0 wt%), far greater than that of pure BT particles (4.7%). Based on the sensitive electroresponsive properties, the PMMA@BT particles have potential applications as electroresponsive materials.

Self-assembled membrane composed of amyloid-like proteins for efficient size-selective molecular separation and dialysis.

The design and scalable construction of robust ultrathin protein membranes with tunable separation properties remain a key challenge in chemistry and materials science. Here, we report a macroscopic ultrathin protein membrane with the potential for scaled-up fabrication and excellent separation efficiency. This membrane, which is formed by fast amyloid-like lysozyme aggregation at air/water interface, has a controllable thickness that can be tuned to 30-250 nm and pores with a mean size that can be tailored from 1.8 to 3.2 nm by the protein concentration. This membrane can retain > 3 nm molecules and particles while permitting the transport of small molecules at a rate that is 1~4 orders of magnitude faster than the rate of existing materials. This membrane further exhibits excellent hemodialysis performance, especially for the removal of middle-molecular-weight uremic toxins, which is 5~6 times higher in the clearance per unit area than the typical literature values reported to date.

Electro-response characteristic of starch hydrogel crosslinked with Glutaraldehyde.

The facile synthesis of the starch hydrogel with anisotropic microstructure and dynamic behaviors was developed in the presence (A-gel) and absence of DC electric field (B-gel). The microstructures of hydrogels were characterized by environmental scanning electron microscope. Their electro-responsive property of hydrogels was investigated with their storage modulus (G'). The result demonstrates that the G' of A-gel is greater than that of B-gel, and the modulus of A-gel increases along with the external field, which signifies positive electroresponse. In addition, the G' of A-gel and B-gel ((G'(A) and G'(B)) also continuously increases with increasing starch concentration, whereas both the maximum of modulus increment (ΔG' = G'(A)−G'(B) ) and that of modulus increment sensitivity (ΔG'/G'(B)) occur with the starch weight fraction at around 36.5%. To enhance the electro-responsive effects of the hydrogels, dielectric particles were dispersed in the hydrogel. It is found that BaTiO3/chitosan core-shell composite particles significantly enhance the electroresponse of the hydrogel. The mechanism of the electro-response mode is proposed.