Development of a simple process to obtain luminescent YVO4:Eu3+ nanoparticles for Fiber Optic Dosimetry

YVO4:Eu3+ is a red emitter phosphor commercially available as micrometric powder due to its high luminescence efficiency under electron-beam excitation. Although some published results have demonstrated the potential of using this micrometer material in Fiber Optic Dosimetry systems, there is no information regarding its use on a nanometric scale. In order to obtain a nanometric material with high luminescent efficiency, a simple synthetic combustion method was developed and the results were compared with both, those of a commercial material and those obtained by a typical coprecipitation synthesis. A single crystalline phase was obtained when the combustion route was employed for the preparation meanwhile two crystalline phases were obtained via coprecipitation synthesis. The particle size of YVO4:Eu3+ obtained by combustion route ranges from 55 up to 200 nm. Fourier Transform Infrared Spectroscopy and Thermogravimetric Analysis indicated that annealing at 600 °C promote the degradation of the impurities that remained adsorbed onto nanoparticles surface after the synthesis. However, to improve the Radioluminescence intensity, an annealing process at 1000 °C was required. The method allows obtaining a nanometric material with a scintillation intensity almost twice higher than that of the commercial powder.Fil: Mentasti, Luciana. Universidad Nacional del Centro de la Provincia de Buenos Aires. Centro de Investigaciones en Física e Ingeniería del Centro de la Provincia de Buenos Aires. - Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tandil. Centro de Investigaciones en Física e Ingeniería del Centro de la Provincia de Buenos Aires. - Provincia de Buenos Aires. Gobernación. Comisión de Investigaciones Científicas. Centro de Investigaciones en Física e Ingeniería del Centro de la Provincia de Buenos Aires; ArgentinaFil: Martínez Clemente, Nahuel Facundo. Universidad Nacional del Centro de la Provincia de Buenos Aires. Centro de Investigaciones en Física e Ingeniería del Centro de la Provincia de Buenos Aires. - Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tandil. Centro de Investigaciones en Física e Ingeniería del Centro de la Provincia de Buenos Aires. - Provincia de Buenos Aires. Gobernación. Comisión de Investigaciones Científicas. Centro de Investigaciones en Física e Ingeniería del Centro de la Provincia de Buenos Aires; ArgentinaFil: Zucchi, Ileana Alicia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; ArgentinaFil: Santiago, Martin Alejo. Universidad Nacional del Centro de la Provincia de Buenos Aires. Centro de Investigaciones en Física e Ingeniería del Centro de la Provincia de Buenos Aires. - Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tandil. Centro de Investigaciones en Física e Ingeniería del Centro de la Provincia de Buenos Aires. - Provincia de Buenos Aires. Gobernación. Comisión de Investigaciones Científicas. Centro de Investigaciones en Física e Ingeniería del Centro de la Provincia de Buenos Aires; ArgentinaFil: Barreto, Gastón Pablo. Universidad Nacional del Centro de la Provincia de Buenos Aires. Centro de Investigaciones en Física e Ingeniería del Centro de la Provincia de Buenos Aires. - Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tandil. Centro de Investigaciones en Física e Ingeniería del Centro de la Provincia de Buenos Aires. - Provincia de Buenos Aires. Gobernación. Comisión de Investigaciones Científicas. Centro de Investigaciones en Física e Ingeniería del Centro de la Provincia de Buenos Aires; Argentin

Block copolymer micelles generated by crystallization-driven self-assembly in polymer matrices

In this review we show how Crystallization-Driven Self-Assembly (CDSA), a method originally employed for the self-assembly of block copolymers in solution, was extended to the synthesis of elongated micellar nanostructures in polymer matrices. By highlighting some of the works published by our group in this area, the conditions to synthesize nanostructured polymers by CDSA are discussed. The knowledge of these conditions will allow developing a new generation of nanomaterials with tailored architecture according to a required application.Fil: Gutiérrez González, Jessica. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; ArgentinaFil: Schmarsow, Ruth Noemí. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; ArgentinaFil: Montoya Rojo, Ursula Maria. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Tecnología en Polímeros y Nanotecnología. Universidad de Buenos Aires. Facultad de Ingeniería. Instituto de Tecnología en Polímeros y Nanotecnología; ArgentinaFil: Puig, Julieta. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; ArgentinaFil: Schroeder, Walter Fabian. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; ArgentinaFil: Zucchi, Ileana Alicia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; Argentin

Remote activation by green-light irradiation of shape memory epoxies containing gold nanoparticles

Shape memory epoxies (SMEs) that can be remotely activated by the use of green light, are described. An epoxy matrix based on on diglycidylether of bisphenol A (DGEBA cured with a mixture of n-dodecylamine (DA) and m-xylylenediamine (MXDA), exhibits excellent shape memory properties as described in a previous paper (Leonardi et al., 2011). Au NPs with an average diameter close to 5 nm could be uniformly dispersed in this matrix using poly(ethylene oxide) (PEO) chains as stabilizer. These NPs showed a significant photothermal effect even at very low concentrations (0.01 wt% as metallic gold), when irradiated with a 532 nm laser at a power close to 2 W/cm2. Under these conditions, a bended bar (1.4-mm thickness) recovered its initial shape in a few seconds. This formulation may be used to build up devices with the necessary mechanical strength and with the possibility to produce shape recovery by remote activation using green light. A second example was analyzed employing an amphiphilic epoxy matrix to produce a uniform dispersion of Au NPs stabilized with dodecyl chains (average diameter close to 3 nm). A bar (1.4-mm thickness) of the SME with 0.04 wt% Au NPs (as metallic gold) showed a fast recovery of its initial shape by irradiation with a 532 nm laser at a power close to 2 W/cm2. This example shows the feasibility of adapting the epoxy chemistry to disperse Au NPs stabilized with different ligands and obtained through robust synthetic methods.Fil: Leonardi, Agustina Belen. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; ArgentinaFil: Puig, Julieta. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; ArgentinaFil: Antonacci, Julian. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Departamento de Física; ArgentinaFil: Arenas, Gustavo Francisco. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Departamento de Física; ArgentinaFil: Zucchi, Ileana Alicia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; ArgentinaFil: Hoppe, Cristina Elena. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; ArgentinaFil: Reven, Linda. McGill University; CanadáFil: Zhu, Liu. Peking University Shenzhen Graduate School; ChinaFil: Toader, Violeta. McGill University; CanadáFil: Williams, Roberto Juan Jose. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; Argentin

Nanoribbons with semicrystalline core dispersed in a visible-light photopolymerized epoxy network

It has been well documented that self-assembly of block copolymers (BCP) in selective solvents, where the core-forming block is a crystallizable polymer, results in micelle structures with exceptional aggregation morphologies determined mainly by the crystallization energy from the core. In this contribution, we apply this concept to create ribbon-like nanostructures dispersed in an epoxy network. The selected system was a polyethylene-b-poly(ethylene oxide) (PE-b-PEO) diblock copolymer in an epoxy monomer based on diglycidyl ether of bisphenol A (DGEBA). This system was selected on the bases that PEO is an epoxy-philic block which is completely miscible with DGEBA before and after curing reaction whereas PE is a crystallizable epoxy-phobic block. Under these conditions, we access to self-assembled nanostructures with semicrystalline core before curing reaction. With the aim of preserving the structural features of these micelles, the epoxy monomers were cured at room temperature (i.e., below the melting transition of the core-forming PE block) by photoinitiated cationic ring-opening polymerization. Long nanoribbons dispersed in the cured epoxy matrix were obtained, as characterized by SAXS patterns and TEM images. These ribbon-like micelles present a tendency to aggregate resulting in the formation of face-to-face stacking of parallel micelles. We demonstrated that while the stacking number decreases with decreasing BCP concentration, the arrangement of the nanoribbons within one stack becomes less organized.Fil: Zucchi, Ileana Alicia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; ArgentinaFil: Schroeder, Walter Fabian. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; Argentin

Microdomain orientation dependence on thickness in thin films of cylinder-forming PS-b-PMMA

The self-assembly of block-copolymer thin films in periodic nanostructures has received considerable attention during the last decade due to their potential applications in nanofabrication and nanolithography. We followed the morphologies developed in thin films of a cylinder-forming diblock copolymer polystyrene-b-poly(methylmethacrylate) ((PS-b-PMMA), PS 46.1 kg mol−1, PMMA 21.0 kg mol−1, lattice spacing L0 = 36 nm), as a function of the film thickness (t), analyzing the effect of thickness commensurability on domain orientation in respect to the substrate. The study was circumscribed to the unexplored range of thickness below L0. Two thickness windows with perpendicular orientation of the PMMA domains were identified: a well-known window at t ~ L0 and a new window at t ~L0/2. A half-parallel cylinder morphology was observed for t ~ ¾ L0 with a progressive change in morphology C┴ → C|| → C┴ when thickness increases from L0/2 to L0. This experimental evidence provides new insights on the mechanism of block copolymers self-organization and indicates the possibility to tune the thickness of the nanostructured polymeric film below L0, allowing the fabrication of ultrathin soft masks for advanced lithographic processes.Fil: Zucchi, Ileana Alicia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; Argentina. Istituto Nazionale per la Fisica della Materia; ItaliaFil: Poliani, Emanuele. Istituto Nazionale per la Fisica della Materia; ItaliaFil: Perego, Michele. Istituto Nazionale per la Fisica della Materia; Itali

Comparison of morphologies and mechanical properties of crosslinked epoxies modified by polystyrene and poly(methyl methacrylate)) or by the corresponding block copolymer polystyrene-b-poly(methyl methacrylate)

Polystyrene (PS, Mn=28,400, PI=1.07), poly(methyl methacrylate) (PMMA, Mn=88,600, PI=1.03), and PS (50,000)-b-PMMA (54,000) (PI=1.04), were used as modifiers of an epoxy formulation based on diglycidyl ether of bisphenol A (DGEBA) and m-xylylene diamine (MXDA). Both PS and PMMA were initially miscible in the stoichiometric mixture of DGEBA and MXDA at 80°C, but were phase separated in the course of polymerization. Solutions containing 5 wt% of each one of both linear polymers exhibited a double phase separation. A PS-rich phase was segregated at a conversion close to 0.02 and a PMMA rich phase was phase separated at a conversion close to 0.2. Final morphologies, observed by scanning electron microscopy (SEM), consisted on a separate dispersion of PS and PMMA domains. A completely different morphology was observed when employing 10 wt% of PS-b-PMMA as modifier. PS blocks with Mn=50,000 were not soluble in the initial formulation. However, they were dispersed as micelles stabilized by the miscible PMMA blocks, leading to a transparent solution up to the conversion where PMMA blocks began to phase separate. A coalescence of the micellar structure into a continuous thermoplastic phase percolating the epoxy matrix was observed. The elastic modulus and yield stress of the cured blend modified by both PS and PMMA were 2.64 GPa and 97.2 MPa, respectively. For the blend modified by an equivalent amount of block copolymer these values were reduced to 2.14 GPa and 90.0 MPa. Therefore, using a block copolymer instead of the mixture of individual homopolymers and selecting an appropriate epoxy-amine formulation to provoke phase separation of the miscible block well before gelation, enables to transform a micellar structure into a bicontinuous thermoplastic/thermoset structure that exhibits the desired decrease in yield stress necessary for toughening purposes.Fil: Zucchi, Ileana Alicia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; ArgentinaFil: Galante, Maria Jose. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; ArgentinaFil: Williams, Roberto Juan Jose. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; Argentin

The change in the enviroment of the immscible block stabilizes an unexpected HPC phase in cured block copolymer/epoxy blend

A conventional SAXS study of ordered phases produced in cured block copolymer (BCP)/epoxy blends with different concentrations, led to the unexpected observation of an HPC (hexagonally-packed cylinders) phase for a blend containing a 55:45 volume ratio of both domains. The BCP was polystyrene (PS, Mn = 28 kDa)-b-poly(ethylene oxide) (PEO, Mn = 11 kDa), where PS is the “epoxy-phobic” block and PEO is the “epoxy-philic” block. The epoxy formulation was based on diglycidylether of bisphenol A (DGEBA) and 4,4′-methylenebis(2,6-diethylaniline) (MDEA). A fully cured blend containing 60 wt% BCP, equivalent to 45% volume fraction of PS in the blend, exhibited an unexpected HPC morphology as supported by TEM images and SAXS spectra. The same techniques showed that a lamellar (L) phase was generated at low conversions in the same blend. The L to HPC transition was explained by the diffusion of epoxy–amine species out of the PS-rich phase with the increase in conversion. Order-order transitions in BCP/epoxy blends previously reported were explained by the partial phase separation of the miscible block from the epoxy solvent. These transitions go always in the sense of decreasing the interface curvature (e.g., from HPC to L). The transition reported in this study goes in the opposite sense (from L to HPC) and was generated by the change in environment of the immiscible block during polymerization.Fil: Leonardi, Agustina Belen. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; ArgentinaFil: Zucchi, Ileana Alicia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; ArgentinaFil: Williams, Roberto Juan Jose. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; Argentin

Surface energies of linear and cross-linked polymers based on isobornyl methacrylate and methacryl-heptaisobutyl POSS

The use of monofunctional polyhedral oligomeric silsesquioxanes (POSS) as polymer modifiers requires controlling the phase separation process producing POSS-rich and polymer-rich domains that occurs in most systems due to the thermodynamic incompatibility between both components. One significant result of this study is the finding that isobornyl methacrylate (IBoMA) is an excellent reactive solvent of a commercial methacryl-heptaisobutyl POSS (MA-POSS). Formulations containing up to 30 wt% MA-POSS in IBoMA or in IBoMA (95 parts by weight)-diethylene glycol dimethacrylate (DEGDMA, 5 parts by weight), were polymerized using benzoyl peroxide as initiator up to complete conversion of C{double bond, long}C bonds (determined by FTIR). Transparent POSS-modified materials were obtained without any evidence of a macroscopic phase separation. POSS addition produced a decrease of the glass transition temperature and the glassy and rubbery elastic modulus. A significant decrease in surface energy for both linear and cross-linked polymers was observed. This effect was particularly important for cross-linked polymers where the addition of 30 wt% POSS decreased the surface energy from about 29 mN m-1 to 16 mN m-1, a very low value for hydrocarbon materials. This study opens a way to obtain hydrophobic methacrylic coatings without the use of fluorinated monomers. © 2008 Elsevier Ltd. All rights reserved.Fil: Zucchi, Ileana Alicia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; ArgentinaFil: Galante, Maria Jose. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; ArgentinaFil: Williams, Roberto Juan Jose. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; Argentin

Thermally reversible light scattering films based on the melting/crystallization of organic crystals dispersed in an epoxy matrix

Films that can be reversibly switched from opaque to transparent states by varying temperature (TRLS films), have potential applications in thermal sensors, optical devices, recording media, etc. A dispersion of organic crystals in a thermoset may be used for these purposes provided that at temperatures higher than the melting point there is a matching of refractive indices of both phases. A model system consisting on a dispersion of diphenyl (DP) crystals in an epoxy matrix based on diglycidyl ether of bisphenol A and m-xylylenediamine, was analyzed as a possible TRLS film encapsulated between transparent covers to avoid sublimation of DP. To obtain a uniform dispersion of DP-rich domains in the epoxy matrix by polymerization-induced phase separation, it was necessary to add 5 wt% of polystyrene (PS) to the initial formulation. Phase separation induced by polymerization at 80 °C led to a dispersion of PS/DP domains in the epoxy matrix due to the low compatibility of PS with the epoxy and its high compatibility with DP. Crystallization and melting processes were confined to the interior of dispersed domains leading to an excellent reproducibility of the optical properties of TRLS films in the course of successive heating–cooling cycles.Fil: Zucchi, Ileana Alicia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; ArgentinaFil: Galante, Maria Jose. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; ArgentinaFil: Williams, Roberto Juan Jose. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; Argentin

Generation of large and locally aligned wormlike micelles in block copolymer/epoxy blends

A dispersion of wormlike micelles, empirically found in some block copolymer (BCP) / epoxy blends, has been reported to produce a significant toughening of epoxy networks. In this study, a rationale procedure to generate and trap large and locally aligned wormlike micelles in an epoxy matrix is reported. A BCP / epoxy / hardener blend was selected that was homogeneous at the polymerization temperature but became nanostructured in the course of polymerization leading to hexagonally packed cylinders (HPC) domains. When a similar BCP with a molar mass about three times larger than the first one and with the same ratio between blocks was used, the nanostructuration into HPC domains was frustrated by diffusional limitations of the large cylindrical micelles generated. A morphology consisting of a dispersion of large and locally aligned wormlike micelles was trapped in the cross-linked epoxy. The selected BCP was polystyrene (PS)-b-poly(ethylene oxide) (PEO), with molar masses M = 43 kDa or 136 kDa and a mass fraction of PEO close to 25 wt %. The network precursors were based on diglycidylether of bisphenol A (DGEBA) and 4,4´-methylenebis(2,6-diethylaniline) (MDEA). Low- and high-molar-mass BCP generated, respectively, HPC domains and wormlike micelles, as supported by TEM images and SAXS spectra.Fil: Leonardi, Agustina Belen. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Mar del Plata. Instituto de Investigación en Ciencia y Tecnología de Materiales (i); Argentina. Universidad Nacional de Mar del Plata. Facultad de Ingeniería; ArgentinaFil: Zucchi, Ileana Alicia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Mar del Plata. Instituto de Investigación en Ciencia y Tecnología de Materiales (i); Argentina. Universidad Nacional de Mar del Plata. Facultad de Ingeniería; ArgentinaFil: Williams, Roberto Juan Jose. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Mar del Plata. Instituto de Investigación En Ciencia y Tecnología de Materiales (i); Argentina. Universidad Nacional de Mar del Plata. Facultad de Ingeniería; Argentin