Projeto interdisciplinar MEL-MAT

O Mel-Mat é um projeto interdisciplinar realizado pelo grupo de bolsistas do subprojeto de Matemática do Pibid, UNIPAMPA, Campus Bagé. Teve como objetivo apresentar a matemática através das abelhas e da apicultura, explorando conhecimentos de geometria plana, geometria espacial e matemática financeira. Além disso, explorou conhecimentos de Biologia, de Química e de Língua Portuguesa que se envolvem no mesmo tema, estimulando a pesquisa, o desenvolvimento crítico do cidadão, a escrita e a conscientização da sustentabilidade do meio ambiente. Para isso, contou com a tecnologia para a construção de planilhas eletrônicas, materiais e ferramentas para a apicultura e o estímulo à pesquisa. Espera-se que, ao final, todos os envolvidos compreendam o tema abordado e percebam a utilidade da Matemática

Globular Clusters around Galaxies in Groups

We have obtained deep photometry of NGC 1199 (in HCG 22) and NGC 6868 (in the Telescopium group). Both galaxies are the optically brightest galaxies of their groups. Our analysis of B and R images taken with the Keck II and the VLT/ESO telescopes, detected a population of globular clusters around both galaxies, with total specific frequencies S_N=1.7\pm0.6 for NGC 1199 and S_N = 1.3\pm0.6 for NGC 6868. The color distributions of the globular cluster systems shows bimodal peaks centered at (B-R)_0 = 1.13\pm0.10 and 1.42\pm0.10 (NGC 1199) and (B-R)_0=1.12\pm0.10 and 1.42\pm0.10 (NGC 6868).Comment: 3 pages, 1 figure. To appear in the proceedings of IAU Symp. 207, "Extragalactic Star Clusters", eds. E. Grebel, D. Geisler, D. Minnit

Effect of particle size and Debye length on order parameters of colloidal silica suspensions under confinement

Dieser Beitrag ist mit Zustimmung des Rechteinhabers aufgrund einer (DFG geförderten) Allianz- bzw. Nationallizenz frei zugänglich.This publication is with permission of the rights owner freely accessible due to an Alliance licence and a national licence (funded by the DFG, German Research Foundation) respectively.Using atomic force microscopy (AFM) and small angle X-ray scattering (SAXS), we show a full comparison between structuring of nanoparticles in confinement and in bulk in order to explain the effect of confinement on characteristic lengths and the scaling law of the characteristic lengths. Three different-sized particle suspensions are used to check the generalization and the correlation between the characteristic lengths and the system parameters, like particle diameter and Debye length. The two characteristic lengths obtained from AFM force curves, the oscillatory wavelength λ, which is related to the average particle distance, and the decay length ξ, which measures how far particle correlates to obtain periodic oscillations, are in good agreement with the mean particle distance 2π/qmax and the correlation length 2/Δq in bulk, respectively, obtained from the structure peaks of SAXS diagrams. Although confinement causes layering of nanoparticles parallel to the confining surfaces, the characteristic lengths in the direction perpendicular to the confining surfaces follow the bulk behavior. The wavelength scales as ρ−1/3 with the particle number density ρ irrespective of the particle size and the ionic strength and shows a pure volume effect. Upon comparing with literature results, the λ = ρ−1/3 scaling law can be applied more generally for charged particles, as long as the repulsive interaction is sufficiently long-ranged, than the previous expression of λ = 2(R + κ−1), which only approaches the value of average particle distance under specific conditions. The decay length ξ is controlled both by the particle size and the ionic strength of the suspensions, and ξ = R + κ−1 is proposed in the paper. In addition, the interaction strength, the force amplitude and maximum scattering intensity, increases linearly with particle concentration. On the other hand, the Monte Carlo (MC) simulations and approximate hypernetted chain (HNC) closure calculation based on Derjaguin-Landau-Verwey-Overbeek (DLVO) potential are employed to study the characteristic lengths from the theoretical point of view. The experimental wavelengths are in good agreement with the theoretical counterparts and the experimental decay lengths show the same qualitative behavior as theoretical ones on the particle size and ionic strength.DFG, SPP 1273, KolloidverfahrenstechnikDFG, GRK 1524, Self-Assembled Soft-Matter Nanostructures at Interface

Structure of PEP-PEO block copolymer micelles: Exploiting the complementarity of small-angle X-ray scattering and static light scattering

The structure of large block copolymer micelles is traditionally determined by small-angle neutron scattering (SANS), covering a large range of scattering vectors and employing contrast variation to determine the overall micelle morphology as well as the internal structure on shorter length scales. The present work shows that the same information can be obtained by combining static light scattering (SLS) and small-angle X-ray scattering (SAXS), which provide information on, respectively, large and short length scales. Micelles of a series of block copolymers of poly(ethylene propylene)-b-poly(ethylene oxide) (PEP–PEO) in a 70% ethanol solution are investigated. The polymers have identical PEP blocks of 5.0 kDa and varying PEO blocks of 2.8–49 kDa. The SLS contrasts of PEP and PEO are similar, providing a homogeneous contrast, making SLS ideal for determining the overall micelle morphology. The SAXS contrasts of the two components are very different, allowing for resolution of the internal micelle structure. A core–shell model with a PEP core and PEO corona is fitted simultaneously to the SAXS and SLS data using the different contrasts of the two blocks for each technique. With increasing PEO molecular weight, a transition from cylindrical to spherical micelles is observed. This transition cannot be identified from the SAXS data alone, but only from the SLS data.</jats:p

Magnetic and elastic anisotropy in magnetorheological elastomers using nickel-based nanoparticles and nanochains

Nickel (Ni) based nanoparticles and nanochains were incorporated as fillers in polydimethylsiloxane (PDMS) elastomers and then these mixtures were thermally cured in the presence of a uniform magnetic field. In this way, macroscopically structured-anisotropic PDMS-Ni based magnetorheological composites were obtained with the formation of pseudo-chains-like structures (referred as needles) oriented in the direction of the applied magnetic field when curing. Nanoparticles were synthesized at room temperature, under air ambient atmosphere (open air, atmospheric pressure) and then calcined at 400 °C (in air atmosphere also). The size distribution was obtained by fitting SAXS experiments with a polydisperse hard spheres model and a Schulz-Zimm distribution, obtaining a size distribution centered at (10.0 - 0.6) nm with polydispersivity given by sigma= (8.0 ± 0.2) nm. The SAXS, XRD and TEM experiments are consistent with single crystal nanoparticles of spherical shape (average particle diameter obtained by TEM: (12 ± 1) nm). Nickel-based nanochains (average diameter: 360 nm; average length: 3 mm, obtained by SEM; aspect ratio=length/diameter ~10) were obtained at 85 ºC and ambient atmosphere (open air, atmospheric pressure). The magnetic properties of Ni-based nanoparticles and nanochains at room temperature are compared and discussed in terms of surface and size effects. Both Ni-based nanoparticles and nanochains were used as fillers for obtaining the PDMS structured magnetorheological composites, observing the presence of oriented needles. Magnetization curves, ferromagnetic resonance spectra (FMR) and strain-stress curves of low filler´s loading composites (2% w/w of fillers) were determined as functions of the relative orientation respect to the needles. The results indicate that even at low loadings it is possible to obtain magnetorheological composites with anisotropic properties, with larger anisotropy when using nanochains. For instance, the magnetic remanence, the FMR-resonance field and the elastic response to compression are higher when measured parallel to the needles (about 30% with nanochains as fillers). Analogously, the elastic response is also anisotropic, with larger anisotropy when using nanochains as fillers. Therefore, all experiments performed confirm the high potential of nickel nanochains to induce anisotropic effects in magnetorheological materials.Fil: Landa, Romina Ailín. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinacion Administrativa Ciudad Universitaria. Instituto de Química Física de los Materiales del Medioambiente y Energía; Argentina;Fil: P Soledad Antonel. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinacion Administrativa Ciudad Universitaria. Instituto de Química Física de los Materiales del Medioambiente y Energía; Argentina;Fil: Mariano M. Ruiz. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinacion Administrativa Ciudad Universitaria. Instituto de Química Física de los Materiales del Medioambiente y Energía; Argentina;Fil: Oscar E Pérez. Universidad de Buenos Aires. Facultad de Cs.exactas y Naturales. Departamento de Industrias;Fil: Alejandro Butera. Comisión Nacional de Energía Atómica;Fil: Guillermo Jorge. Universidad Nacional de General Sarmiento;Fil: Cristiano L. P. Oliveira. Instituto de Física, Universidade De São Paulo; Brasil;Fil: Martín Negri. Universidad de Buenos Aires. Facultad de Cs.exactas y Naturales. Departamento de Industrias

Divalent Cations and Redox Conditions Regulate the Molecular Structure and Function of Visinin-Like Protein-1

The NCS protein Visinin-like Protein 1 (VILIP-1) transduces calcium signals in the brain and serves as an effector of the non-retinal receptor guanylyl cyclases (GCs) GC-A and GC-B, and nicotinic acetyl choline receptors (nAchR). Analysis of the quaternary structure of VILIP-1 in solution reveals the existence of monomeric and dimeric species, the relative contents of which are affected but not exclusively regulated by divalent metal ions and Redox conditions. Using small-angle X-ray scattering, we have investigated the low resolution structure of the calcium-bound VILIP-1 dimer under reducing conditions. Scattering profiles for samples with high monomeric and dimeric contents have been obtained. The dimerization interface involves residues from EF-hand regions EF3 and EF4