This letter reports the synthesis and characterization of functionalized magnetic nanoparticles associated with chemical gels and their application to the conservation of cultural heritage. Magnetic nanoparticles, which are associated with acrylamide ethylene oxide polymers, produce a sponge that can be loaded with oil-in-water microemulsions, forming a magnetically responsive gel-like system and acting as a permanent hydrogel. The magnetic gel-like system can be used for specific applications in detergents or in the release of the loaded material. The system can be magnetically manipulated and cleaned from the loaded materials and then dried and reused for a different application. We report an important application of this new nanomagnetic responsive material in the field of cultural heritage conservation.
Nanocomposite materials consisting of CoFe2O4 magnetic nanoparticles and a polyethylene glycol-acrylamide gel matrix have been synthesized. The structure of such materials was studied by means of small-angle scattering of X-rays and polarized neutrons, showing that the CoFe2O4 nanoparticles were successfully and homogeneously embedded in the gel structure. Magnetic, viscoelastic, and water retention properties of the nanocomposite gel confirm that the properties of both nanoparticles and gel are combined in the resulting nanomagnetic gel. Scanning electron microscopy highlights the nanocomposite nature of the material, showing the presence of a gel structure with different pore size distributions (pores with micron and nano-size distributions) that can be used as active sponge-like nanomagnetic container for water-based formulations as oil-in-water microemulsions.
In hybrid organic solar cells a blocking layer between transparent electrode and nanocrystalline titania particles is essential to prevent short-circuiting and current loss through recombination at the electrode interface. Here we report the preparation of a thin, uniform and crack free hybrid blocking layer composed of conducting titania nanoparticles embedded in an insulating polymer derived ceramic. To do so we combine sol-gel chemistry with novel poly(dimethylsiloxane) containing amphiphilic block copolymer, poly(ethyleneglycol) methyl ether methacrylate-block-poly(dimethylsiloxane)-blockpoly(ethyleneglycol) methyl ether methacrylate as the templating agent. Conductive probe scanning force microscopy proved that the existing percolating titania networks are separated by an insulating ceramic matrix. The structural uniformity of the percolating structures was investigated by microbeam grazing incidence small angle X-ray scattering making the integrated blocking layer suitable for hybrid organic solar device applications. Preliminary tests with the integrated blocking layer showed reasonable comparison to conventional TiO 2 blocking layer containing devices mentioned in the literature.
Titania nanoparticles are prepared by sol–gel chemistry with a poly(ethylene oxide) methyl ether methacrylate-block-poly(dimethylsiloxane)-block-poly(ethylene oxide) methyl ether methacrylate triblock copolymer acting as the templating agent. The sol–gel components—hydrochloric acid, titanium tetraisopropoxide, and triblock copolymer—are varied to investigate their effect on the resulting titania morphology. An increased titania precursor or polymer content yields smaller primary titania structures. Microbeam grazing incidence small-angle X-ray scattering measurements, which are analyzed with a unified fit model, reveal information about the titania structure sizes. These small structures could not be observed via the used microscopy techniques. The interplay among the sol–gel components via our triblock copolymer results in different sized titania nanoparticles with higher packing densities. Smaller sized titania particles, (∼13–20 nm in diameter) in the range of exciton diffusion length, are formed by 2% by weight polymer and show good crystallinity with less surface defects and high oxygen vacancies.
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