Abnormal activity of functional groups during uranyl ions sorption by polymethacrylic acid-poly-4-vinylpyridine intergel system

Uranyl ions sorption by intergel system consisting of polymethacrylic acid hydrogel (hPMAA) and poly-4-vinylpyridine hydrogel (hP4VP) has been studied. First, reciprocal activation of PMAA and P4VP polymeric hydrogels in water environment was examined in order to predict intergel system sorption activity. Based on the obtained results, it was found that area of maximum hydrogel activation was within the ratios of 100 % hPMAA and 67 % hPMAA:33 % hP4VP. The maximum rate of uranyl ions extraction was also observed within these ratios. The highest uranyl ions sorption by intergel system occurred at 83 %hPMAA:17 % hP4VP ratio. Maximum uranyl ions extraction rate after 56 hours of hydrogels remote interaction was 82.5 %, when polymeric chain binding rate was 9.94 % and effective dynamic exchange capacity was 1.12 mmol/g. Significant increase of intergel system sorption activity within the ratios of 100 % hPMAA and 67 % hPMAA:33 % hP4VP in comparison with initial inactivated hydrogels 100 % hPMAA and 100 % hP4VP was confirmed by combined calculation data of extraction rates of inactivated PMAA and P4VP polymeric hydrogels. The obtained results illustrated changes of initial polymeric hydrogels’ electrochemical sorption properties in intergel system leading to functional groups obtaining higher reactive ability, which made it possible to use them for further development of highly efficient uranyl ions extraction sorption technology

Novel Amphiphilic Polyfluorene-Graft-(Polymethacrylic Acid) Brushes: Synthesis, Conformation, and Self-Assembly

Novel polyfluorene polymer brushes with polymethacrylic acid side chains were obtained by atom transfer radical polymerization (ATRP) and activator generated by electron transfer (AGET) ATRP of tert-butyl methacrylate on polyfluorene multifunctional macroinitiator, followed by protonolysis of the tert-butyl groups of the side chains. Kinetics of polymerization and molecular weights were fully characterized. These polymer brushes luminesce in the blue region of the spectrum with high quantum yields (0.64–0.77). It was shown that the luminescence intensity of polymer brushes is higher than the luminescence intensity of the macroinitiator (0.61). Moreover, due to their amphiphilic nature, they can form unimolecular micelles when an alcohol solution of the polymer brush is injected into water. These properties can potentially be used in drug delivery and bioimaging.

FEATURES OF SORPTION OF URANYL IONS BY POLYMETHACRYLIC ACID-POLY-4-VINYLPYRIDINE INTERPOLYMER SYSTEM

The sorption extraction of uranyl ions by interpolymer system consisting of polymethacrylic acid hydrogel (hPMAA) and poly-4-vinylpyridine hydrogel (hP4VP) was studied. Sorption and kinetic characteristics of initial polymers and hPMAA-hP4VP intergel system were determined. Maximum uranyl ions extraction rate - 82,8% - is observed in interpolymer system within the ratios of 100% hPMAA and 67% hPMAA:33%hP4VP 56 hours later,when polymeric chain binding rate was 9,97% and effective dynamic exchange capacity was 1,15mmol/g. Obtained outcomes show changes of initial polymeric hydrogels sorption properties ininterpolymer system, which makes it possible to use them for further development of highly efficient uranyl ions extraction sorption technology.