RESUMO
Dual pH- and thermo-responsive polysulfone (PSf) membranes with three-dimensionally interconnected networks are fabricated by introducing poly(acrylic acid-co-N-isopropylacrylamide) (P(AA-NIPAm)) into the membrane surfaces and pore walls during membrane formation via a vapor-liquid induced phase separation (V-LIPS) process. After introducing the copolymers of P(AA-NIPAm), the fabricated membranes exhibit impressive open network pores on the surfaces, meanwhile their cross-sectional structure turns from classical asymmetric finger-like structure into bi-continuous nanopores throughout the whole thickness of membrane, due to high solution viscosity and low mass transfer rate of VIPS process. Furthermore, pure water permeation tests show that the pure water permeation (Lp) and the molecular weight cutoff (MWCO) of the fabricated PSf/P(AA-NIPAm) membranes increases sharply as the solution pH decreases from 12.5 to 1.5 and the feed temperature increases from 25 to 50⯰C, attributing to the increasing pore size. With the decreasing mass ratio of AA to NIPAm, the pH-responsive coefficient decreases, while the temperature- responsive coefficient increases. In particular, for the fabricated membrane with the mass ratio of AA to NIPAm of 3 to 2, Lp changes from â¼16.0 to â¼821.4â¯Lâ¯m-2â¯h-1â¯bar-1 and MWCO increases from â¼223.1 to â¼1493.2â¯kDa, as the filtration experiments are operated with feed pH and temperature of 12.5/25⯰C and 1.5/50⯰C respectively. The results proposed in this study provide a novel mode for design and development dual responsive porous membranes in situ, which will enable good separation of various materials and expand the scope of membrane applications.
RESUMO
In situ pegylated (PEGylated) microporous membranes have been extensively reported using poly(ethylene glycol) (PEG)-based polymers as blending additives. Alternatively, free standing PEGylated polysulfone (PSf) membranes with excellent hydrophilicity and antifouling ability were directly fabricated from polysulfone/poly(ethylene glycol) methyl ether methacrylate (PSf/PEGMA) solutions after in situ cross-linking polymerization without any treatment via vapor induced phase separation (VIPS) process for the first time. The microstructures and performances of the resulting membranes shifted regularly by adjusting exposure time of the liquid film in humid air. With increasing exposure time, plenty of worm-like networks formed and distributed on membrane surfaces, meanwhile cross-sectional morphology changed from asymmetric finger-like microporous structure to symmetric cellular-like structure, resulting in better mechanical stability. As the exposure time raised from 0 to 5â¯min, the surface coverage of carboxyl groups increased from â¼1.1 to 4.0â¯mol%, leading to the decrease in water contact angle from â¼63 to 27° and the increase in water flux from â¼110 to 512â¯Lâ¯m-2â¯h-1. In addition, at prolonged exposure time, increasing hydrophilic PEG chains migrated to membrane surfaced and repelled the adsorption and deposition of protein, resulting in better antifouling ability. The findings of this study offer a facile and high efficient strategy for flexible design and fabrication of the in situ PEGylated membranes with desirable structures and performances in large scale.
RESUMO
This article reported the electrochemical behaviors of a novel hollow carbon microspheres/manganese dioxide nanosheets (micro-HC/nano-MnO2) composite prepared by an in situ self-limiting deposition method under hydrothermal condition. The results of scanning electron microscopy reveal that MnO2 nanosheets homogeneously grow onto the surface of micro-HC to form a loose-packed microstructure. The quantity of MnO2 required in the electrode layer has thereby been reduced significantly, and higher specific capacitances have been achieved. The micro-HC/nano-MnO2 electrode presents a high capacitance of 239.0 F g-1 at a current density of 5 mA cm-2, which is a strong promise for high-rate electrochemical capacitive energy storage applications.