Publications by authors named "Antonio Tavera-Vazquez"

The optical properties of liquid crystals serve as the basis for display, diagnostic, and sensing technologies. Such properties are generally controlled by relying on electric fields. In this work, we investigate the effects of microfluidic flows and acoustic fields on the molecular orientation and the corresponding optical response of nematic liquid crystals.

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Many crystallization processes, including biomineralization and ice-freezing, occur in small and curved volumes, where surface curvature can strain the crystal, leading to unusual configurations and defect formation. The role of curvature on crystallization, however, remains poorly understood. Here, we study the crystallization of blue phase (BP) liquid crystals under curved confinement, which provides insights into the mechanism by which BPs reconfigure their three-dimensional lattice structure to adapt to curvature.

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This review paper presents a procedure for measuring the mesoscopic scales in micellar solutions embedded with giant cylindrical micelles using the mean square displacement determined with a quasi-elastic multiple light scattering method (diffusing wave spectroscopy) and theory. The mesoscopic scales of interest are the micelles' total contour length, persistence and entanglement lengths, and the mesh size of the entangled micellar network. All of them depend on the physicochemical parameters of the solutions and determine the rheological behavior.

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Chromophores susceptible to light-induced trans-cis isomerization embedded in cylindrical micelles can modify micelles and their light-responsive performance. A small chromophore (4-(phenylazo)benzoate ion) is embedded in cylindrical micelles made of cetyltrimethylammonium bromide (CTAB) and sodium salicylate (NaSal) in water. The microstructure is examined by scanning electron microscopy (SEM) and nuclear magnetic resonance (NMR).

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A diblock copolymer made of poly(1,4-butadiene)-block-polyethylene oxide, with a degree of polymerization of the polybutadiene and polyethylene oxide blocks of 37 and 57, respectively, self-assembles in water as worm-like micelles determined by small angle neutron scattering with an average diameter of ∼12.7 nm, a core radius of ∼2.7 nm, a shell radius of ∼3 nm, and an estimated persistence length of >225 nm.

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We present the detailed rheological changes that occur when small quantities of single-wall carbon nanotubes are dispersed in a poly(acrylic acid) water solution, around the overlap polymer concentration, up to the gel point. Here, pH is used to tune the gel formation. Suspensions of nanotubes at pH ≤ 5 are exfoliated and dispersed by the polymer.

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