In all cases the silk powders absorbed metal ions faster than their respective silk fibers. Intensive degumming of the fibers and powders significantly reduced the time to absorb respective metal ions and the time to reach equilibrium was reduced from hours to 5-15 min at pH 8. Once bound, 45-100% of the metal ions were released from the sorbents after exposure to pH 3 buffer for 30 min. The transition metal ion loading capacity for the silk sorbents was considerably higher than that found for commercial ion exchange resins (AG MP-50 and AG 50W-X2) under similar conditions. Interestingly, total Cu2+ bound was found to be higher than theoretically predicted values based on known
specific Cu2+ binding sites
www.selleckchem.com/products/salubrinal.html (AHGGYSGY), suggesting that additional (new) sites for transition metal ion binding sites are present in silk fibers. (C) 2010 Wiley Periodicals, Inc. J Appl Polym Sci 119: 3630-3639, 2011″
“Thanks to their large electrical field-induced strains, electroactive polymers can be used in various applications; as electroactive materials for artificial muscles or as active materials of membranes, due to their flexibility. One drawback concerning their use involves the saturation of the electrical field-induced strain which occurs at around 20% for a polymer film with a thickness of 80 mu m. Few studies CX-6258 manufacturer have been devoted to the understanding of this saturation. To this end, the present paper describes mechanical measurements of the extensive strain versus stress and the determination of the current selleck chemical flowing through an electroactive polymer driven by an electrical field. These experiments have clearly demonstrated that the observed saturation of the electrical induced strain was not due to a mechanical saturation
within the sample but to the saturation of the electrically induced polarization. By carrying out a suitable modeling of the polarization versus electrical field, it was possible to calculate the strain and current versus electrical field. These values were then compared to experimental data, and were found to show a very good agreement. (C) 2010 American Institute of Physics. [doi: 10.1063/1.3504601]“
“Nanofibers of poly(vinylidene fluoride-trifluoroethylene)/polyaniline-polystyrene sulfonic acid (PVDF-TrFE/PANi-PSSA) were fabricated in air at room temperature using electrospinning, with the thinnest fiber having a diameter of similar to 6 nm. This is a cheap, fast, and reliable process for generating PVDF-TrFE/PANi-PSSA composite nanofibers. The presence of conducting PANi-PSSA increased the charge density of the solution and assisted in the fabrication of PVDF-TrFE nanofibers at low polymer concentrations in dimethylformamide without the beading effect. Ultraviolet and visible spectroscopy showed that PANi-PSSA was well incorporated into the PVDF-TrFE solution with no polymer segregation or degradation.