The quality of polymer composite materials depends on the distribution of the filler in the polymer matrix. Due to the presence of the oxygen functional groups, graphene oxide (GO) has a strong affinity to epoxy resins, providing potential opportunity for the uniform distribution of GO sheets in the matrix. Another advantage of GO over its nonoxidized counterpart is its ability to exfoliate to single-atomic-layer sheets in water and in some organic solvents. However, these advantages of GO have not yet been fully realized due to the lack of the methods efficiently introducing GO into the epoxy resin. Here we develop a novel homogeneous liquid phase transfer method that affords uniform distribution, and fully exfoliated condition of GO in the polymer matrix. The most pronounced alteration of properties of the cured composites is registered at the 0.10%-0.15% GO content. Addition of as little as 0.10% GO leads to the increase of the Young's modulus by 48%. Moreover, we demonstrate successful introduction of GO into the epoxy matrix containing an active diluent-modifier; this opens new venues for fabrication of improved GO-epoxy-modifier composites with a broad range of predesigned properties. The experiments done on reproducing the two literature methods, using alternative GO introduction techniques, lead to either decrease or insignificant increase of the Young's modulus of the resulting GO-epoxy composites.
Microcapsules, made of biodegradable polymers, containing magnetite nanoparticles with tunable contrast in both the T1 and T2 MRI modes, were successfully prepared using a layer-by-layer approach. The MRI contrast of the microcapsules was shown to depend on the distance between magnetite nanoparticles in the polymeric layers, which is controlled by their concentration in the microcapsule shell. A fivefold increase in the average distance between the nanoparticles in the microcapsule shell led to a change in the intensity of the MR signal of 100% for both the T1 and T2 modes. Enzyme treatment of biodegradable shells resulted in a change of the microcapsules' MRI contrast. In vivo degradation of nanocomposite microcapsules concentrated in the liver after intravenous injection was demonstrated by MRI. This method can be used for the creation of a new generation of drug delivery systems, including drug depot, with combined navigation, visualization and remote activated release of bioactive substances in vivo.
The sorption capacity of graphene oxide (GO) toward different metal cations has been the subject of several recent studies. However, the reported quantitative data are controversial, and the mechanism of chemical bonding between GO and metal cations is poorly understood. Clarifying these questions can eventually help to reveal the fine chemical structure of GO that remains ambiguous. In this work, we study the binding of Gd and Mn by GO in the presence of several competing metal cations by the H NMR relaxation method. As a general trend, the efficiency of the metal cations to bind to GO increases with ionic charge, and depends on their ability to form coordinate-covalent bonds with GO oxygen groups. The efficiency of the competing metal cations to "replace" Gd and Mn increases in the order Na < Cs < Ca < Sr < Ga < Lu. GO contains two different types of binding sites, bonding to which results in either high or low NMR relaxivity of the resulting Gd-GO and Mn-GO solutions. Gd and Mn, being replaced from the high-relaxivity sites by the large excess of competing cations, are not released into the bulk solution, but only migrate to the low-relaxivity sites, remaining covalently bonded to GO. The absolute majority of the existing carboxyl groups in GO are located at tiny few-carbon-atom-vacancy defects on the major planes. The density of these vacancy defects is estimated as one per every 200 carbon atoms.
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