Influence of drop volume on surface tension evaluated using the pendant drop method

The pendant drop technique is one of the most accurate methods to measure surface tension of liquids. Recently, it has been found that the value of the surface/interfacial tension found using the pendant drop method might be drop-volume dependent. In this work, the surface tension of glycerol at a 25 °C and the surface tension of polypropylene at 240 °C were measured using the pendant drop method for different drop volumes. It was shown that the values of the surface tension depend on the drop size if no calibration to take into account the anisotropy in the optical enlargement is performed. However, when a calibration procedure for optical anisotropy correction is performed, the values of the surface tension obtained do not depend on the volume drop size and they corroborate the values in the literature.     

Role of urea in the preparation of highly porous nanocomposite aerogels

The preparation of highly porous CoFe2O4-SiO2 nanocomposite aerogels was successfully achieved by a novel sol-gel procedure involving urea-assisted co-gelation of the precursor phases. This method allows fast gelation, giving rise to an aerogel with 97% porosity. The formation of CoFe2O4 nanocrystals homogeneously distributed within the matrix occurs after calcination at 750 degrees C and is complete at 900 degrees C. Despite the high temperature required for the formation of the CoFe2O4 nanocrystals, the high porosity typical of aerogels is still retained.     

Nonlinear optical properties of tetrapyrazinoporphyrazinato indium chloride complexes due to excited-state absorption processes

The multiphoton absorption properties of the axially substituted tetrapyrazinotetraazaporphyrinato complex Pyz(4)TAPInCl (1) are reported and interpreted. In particular, the nonlinear optical transmission of the complex and the excited states involved in the nonlinear absorption have been determined at the frequency of the second harmonic generation of a Nd:YAG laser in the nanosecond time regime. Pyz(4)TAPInCl has an excited-state absorption cross section larger than its ground state in the 460-540 nm spectral region, and it shows an optical limiting (OL) behavior at 532 nm, which derives from a sequential two-photon absorption with a larger absorption cross section of the excited triplet state with respect to the ground state. It results that the absorption cross section of 1 in the excited triplet state is 7.8 x 10(-18) cm(2) vs 0.9 x 10(-18) cm(2) of the ground state at the wavelength of OL analysis.     

Zirconium phosphate/phosphonate multilayered films based on push-pull stilbazolium salt: synthesis, characterization and second harmonic generation

The preparation of materials featuring enhanced second harmonic generation (SHG) values by self-assembly of molecules characterized by high second-order non-linear optic (NLO) activity is nowadays an important and challenging field of research. In order to show SHG the material must have an acentric structure with the dipoles of the molecular components oriented in the same direction and this is synthetically fairly difficult to achieve. This study describes the synthesis of the push-pull stilbazolium salt and its assembly in multilayered acentric thin films, on quartz glass surface, by using the zirconium phosphate/phosphonate (Zr-PO(x)) technique. A particular care has been paid to the optimization of the surface preparation and of the deposition conditions. This allows to obtain highly homogeneous lamellar inorganic-organic materials showing satisfactory second harmonic generation (SHG) values together with high chemical, thermal and mechanical stabilities which are necessary for their integration in optoelectronic devices.     

TiO2 Synthesis by the Pechini’s Method and Application for Diclofenac Photodegradation†

In this work, the effect of the calcination temperature on the TiO₂ synthesis using Pechini’s method was reported. The adopted calcination temperatures were 500, 600, and 700°C. XRD measurements indicated the composition of crystalline phases, and from there, the conversion of the anatase phase to rutile. TiO₂ Evonik^® was used as a reference standard and sodium diclofenac as a standard for photodegradation assessment. The average crystalline size increased. In both cases, this trend accompanied the increase in calcination temperature. The optical properties were performed using diffuse UV‐Vis reflectance. Results obtained indicated maximum absorption wavelength values more intense and displaced to the visible region. Also, the estimated band gap energy values decreased. The photocatalytic performance of TiO₂ samples was superior to the reference catalyst (TiO₂ Evonik^®). Especially in the first 10 minutes, the comparative photodegradation was up to approximately 58% higher. The photodegradation kinetic constants were also higher, and by comparison, up to approximately 73% higher. Toxicity measurements, using Artemias salina, also indicated similar decay behavior in the first 10 minutes, with a performance of up to approximately 60%.     

Molecular dynamics simulation study of solvent effects on conformation and dynamics of polyethylene oxide and polypropylene oxide chains in water and in common organic solvents

In this paper, the conformation and dynamics properties of polyethylene oxide (PEO) and polypropylene oxide (PPO) polymer chains at 298 K have been studied in the melt and at infinite dilution condition in water, methanol, chloroform, carbon tetrachloride, and n-heptane using molecular dynamics simulations. The calculated density of PEO melt with chain lengths of n = 2, 3, 4, 5 and, for PPO, n = 7 are in good agreement with the available experimental data. The conformational properties of PEO and PPO show an increasing gauche preference for the O-C-C-O dihedral in the following order water>methanol>chloroform>carbon tetrachloride = n-heptane. On the contrary, the preference for trans conformation has a maximum in carbon tetrachloride and n-heptane followed in the order by chloroform, methanol, and water. The PEO conformational preferences are in qualitative agreement with results of NMR studies. PEO chains formed different types of hydrogen bonds with polar solvent molecules. In particular, the occurrence of bifurcated hydrogen bonding in chloroform was also observed. Radii of gyration of PEO chains of length larger than n = 9 monomers showed a good agreement with light scattering data in water and in methanol. For the shorter chains the observed deviations are probably due to the enhanced hydrophobic effects caused by the terminal methyl groups. For PEO the fitting of end-to-end distance distributions with the semi-flexible chain model at 298 K provided persistence lengths of 0.375 and 0.387 nm in water and methanol, respectively. Finally, the radius of gyration of Pluronic P85 turned out to be 2.25 ± 0.4 nm at 293 K in water in agreement with experimental data.     

Ab initio calculation of magnetic shielding and susceptibility. Finite perturbation calculation of susceptibility with GIAO's

The magnetic susceptibility of hydrogen fluoride is calculated with four different basis sets of gauge invariant atomic orbitals (GIAO's). The Roothaan equations are solved for various values of the magnetic field strength and the susceptibility is deduced by a numerical differentiation of the energy.     

Foliations by curves on threefolds

We study the conormal sheaves and singular schemes of one-dimensional foliations on smooth projective varieties X of dimension 3 and Picard rank 1. We prove that if the singular scheme has dimension 0, then the conormal sheaf is μ-stable whenever the tangent bundle $TX$ is stable, and apply this fact to the characterization of certain irreducible components of the moduli space of rank 2 reflexive sheaves on ${\mathbb{P}}^3$ and on a smooth quadric hypersurface $Q_3\subset {\mathbb{P}}^4$. Finally, we give a classification of local complete intersection foliations, that is, foliations with locally free conormal sheaves, of degree 0 and 1 on Q₃.