Magnetoelectric nanocomposite films composed of magnetostrictive CoFe 2 O 4 nanoparticles with sizes between 35 and 55 nm embedded in P(VDF-TrFE) have been successfully prepared by a solvent casting method. The ferroelectric, piezoelectric, magnetic and magnetoelectric properties of the nanocomposite and their variation with the wt% of the ferrite filler, thickness of the composite and direction of the applied magnetic field have been investigated. Ferroelectric and piezoelectric properties are improved when small amount of ferrite nanoparticles were added to the polymeric matrix. Magnetic properties vary linearity with ferrite content. The highest magnetoelectric response of 41.3 mV/cmOe was found in the composite with 72wt% when a 2.5 kOe DC field was transversely applied to the sample surface. This value is among the highest reported in two phase particulate polymer nanocomposites. Thickness of the composite has no influence in the magnetoelectric response, allowing tailoring sensor thickness for specific applications. The good value of the magnetoelectric coefficient and the flexibility of the films make these composites suitable for applications in magnetoelectric smart devices.

Bacterial cellulose (BC) produced by some bacteria, among them Gluconacetobacter xylinum, which secrets an abundant 3D networks fibrils, represents an interesting emerging biocompatible nanomaterial. Since its discovery BC has shown tremendous potential in a wide range of biomedical applications, such as artificial skin, artificial blood vessels and microvessels, wound dressing, among others. BC can be easily manipulated to improve its properties and/or functionalities resulting in several BC based nanocomposites. As example BC/collagen, BC/gelatin, BC/Fibroin, BC/Chitosan, etc. Thus, the aim of this review is to discuss about the applicability in biomedicine by demonstrating a variety of forms of this biopolymer highlighting in detail some qualities of bacterial cellulose. Therefore, various biomedical applications ranging from implants and scaffolds, carriers for drug delivery, wound-dressing materials, etc. that were reported until date will be presented.

An enantiopure, conductive, and paramagnetic crystalline 3-D metal−organic framework (MOF), based on Dy(III) and the L-tartrate chiral ligand, is proved to behave as an almost ideal electron spin filtering material at room temperature, transmitting one spin component only, leading to a spin polarization (SP) power close to 100% in the ±2 V range, which is conserved over a long spatial range, larger than 1 μm in some cases. This impressive spin polarization capacity of this class of nanostructured materials is measured by means of magnetically polarized conductive atomic force microscopy and is attributed to the Chirality-Induced Spin Selectivity (CISS) effect of the material arising from a multidimensional helicity pattern, the inherited chirality of the organic motive, and the enhancing influence of Dy(III) ions on the CISS effect, with large spin−orbit coupling values. Our results represent the first example of a MOF-based and CISS-effect-mediated spin filtering material that shows a nearly perfect SP. These striking results obtained with our robust and easy-to-synthesize chiral MOFs constitute an important step forward in to improve the performance of spin filtering materials for spintronic device fabrication.

The poly(styrene)-b-poly(ethylene oxide) (SEO) amphiphilic block copolymer, with two different molecular weights, has been used as a structure directing agent for generating nanocomposites of TiO(2)/SEO via the sol-gel process. SEO amphiphilic block copolymers are designed with a hydrophilic PEO-block which can interact with inorganic molecules, as well as a hydrophobic PS-block which builds the matrix. The addition of different amounts of sol-gel provokes strong variations in the self-assembled morphology of TiO(2)/SEO nanocomposites with respect to the neat block copolymer. As confirmed by atomic force microscopy (AFM), TiO(2)/PEO-block micelles get closer, forming well-ordered spherical domains, in which TiO(2) nanoparticles constitute the core surrounded by a corona of PEO-blocks. Moreover, for 20 vol% sol-gel the generated morphology changes to a hexagonally ordered structure for both block copolymers. The cylindrical structure of these nanocomposites has been confirmed by the two-dimensional Fourier transform power spectrum of the corresponding AFM height images. Affinity between titanium dioxide precursor and PEO-block of SEO allows us to generate hybrid inorganic/organic nanocomposites, which retain the optical properties of TiO(2), as evaluated by UV-vis spectroscopy.

A strain isolated from Kombucha tea was isolated and used as an alternative bacterium for the biosynthesis of bacterial cellulose (BC). In this study, BC generated by this novel bacterium was compared to Gluconacetobacter xylinus biosynthesized BC. Kinetic studies reveal that Komagataeibacter rhaeticus was a viable bacterium to produce BC according to yield, thickness and water holding capacity data. Physicochemical properties of BC membranes were investigated by UV-vis and Fourier transform infrared spectroscopies (FTIR), thermogravimetrical analysis (TGA) and X-ray diffraction (XRD). Additionally, scanning electron microscopy (SEM) and atomic force microscopy (AFM) were also used for morphological characterization. Mechanical properties at nano and macroscale were studied employing PeakForce quantitative nanomechanical property mapping (QNM) and dynamic mechanical analyzer (DMA), respectively. Results confirmed that BC membrane biosynthesized by Komagataeibacter rhaeticus had similar physicochemical, morphological and mechanical properties than BC membrane produced by Gluconacetobacter xylinus and can be widely used for the same applications.

Combining modeling and experiment, we created multilayered gels where each layer was "stacked" on top of the other and covalently interconnected to form mechanically robust materials, which could integrate the properties of the individual layers. In this process, a solution of new initiator, monomer, and cross-linkers was introduced on top of the first gel, and these new components then underwent living (co)polymerization to form the subsequent layer. We simulated this process using dissipative particle dynamics (DPD) to isolate factors that affect the formation and binding of chemically identical gel as well as incompatible layers. Analysis indicates that the covalent bond formation between the different layers is primarily due to reactive chain-ends, rather than residual cross-linkers. In the complementary experiments, we synthesized multilayered gels using either free radical (FRP) or atom transfer radical polymerizations (ATRP) methods. Polymerization results demonstrated that chemically identical materials preserved their structural integrity independent of the polymerization method. For gels encompassing incompatible layers, the contribution of reactive chain-ends plays a particularly important role in the integrity of the material, as indicated by the more mechanically robust systems prepared by ATRP. These studies point to a new approach for combining chemically distinct components into one coherent, multifunctional material as well as an effective method for repairing severed gels. ■ INTRODUCTIONMultifunctional materials address a number of vital technological needs since they allow one material to provide a range of properties and behavior. A challenge in creating these desirable materials is devising an approach for integrating the different components into one cohesive system. Conceptually, one would like to stack the components with different functionalities on top of each other to form the desired product. This approach would have the distinct advantage that it permits new functionalities to be added at will to improve or tailor the utility of the material. To date, however, it remains a considerable challenge to create "stackable materials" that would form a mechanically robust structure. As a step in addressing this challenge, herein we use computational modeling and experimental studies to design multilayered, "stackable" gels, where one layer is effectively "stacked" on top of another. Each gel layer is covalently bound to the neighboring gels, and hence, the system displays considerable mechanical integrity.It is important to recall that researchers have devised means of "gluing" together separated pieces of polymer gels. 1 Recently, Leibler et al. used nanoparticles as a binding agent to successfully attach two severed gels 1b and in this way could heal broken samples. Rather than binding separated sections, our aim is to grow one gel layer on top of another and, thereby, unite chemically distinct gels into a coherent material. Through this approach, we can, for example, stack a hydrophobic ge...

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A B S T R A C TKomagataeibacter rhaeticus, a bacterium isolated from Kombucha tea, was used to produce bacterial cellulose (BC) through its cultivation in a static sugarcane molasses (SCM) supplemented-culture medium (totally or partially), as an alternative carbon source. BC membranes were characterized by different physicochemical analysis using Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), field emission gunscanning electron microscopy (FEG-SEM), thermogravimetry analysis (TGA) and PeakForce quantitative nanomechanics atomic force microscopy (PeakForce (QNM-AFM)). FTIR, XRD and TGA results suggest great similarity among all membranes produced by distinct culture media. Although the glucose (F1) and SCM (F6) media presented the lowest BC yield, all SCM-supplemented culture media (from F2 to F5) showed BC yield values similar to the HS culture medium (F0). FEG-SEM analysis showed that as higher SCM concentrations on culture media higher dense nanofibers network could be prepared. Quantitative nanomechanical results obtained by AFM technique corroborate FEG-SEM analysis besides show smoother and more flexible BC membranes as a function of the increasing of the SCM concentrations. The modification of the carbon source of the culture medium with an important by-product of Brazilian agroindustry appears as a viable alternative to reduce cost of BC production (of up to 20.06%) besides increase the possibilities of industrial scale BC preparation.