Partially coherent optical processor for enhancement of partial second order derivatives of an image: Analysis and implementation

We present an optical processor capable to perform partial second derivatives of an image working with partially coherent illumination. The proposed system utilizes a liquid crystal display, onto which images to be derived are displayed. The method is based on the capacity of these devices to generate simultaneously a contrast reverted replica of the image displayed on it. A positive replica of original image is obtained when the LCD is between crossed polarizers, while the negative one is obtained with the LCD is between parallel polarizers. Since the LCD is a diffraction element, both polarizer arrangements may be simultaneously implemented, for example, in a 4f optical processor using polarization filtering of the different diffraction orders. When three images (two replicas of original image displaced in opposite direction and the other one with contrast reverted and centered at the origin.) are imagined across a slightly defocused plane, one obtains an image with enhanced second derivatives in a given direction. No other incoherent (or partially coherent) optical system is presently known which can perform partial second-order derivatives of an image. Experimental results obtained are presented.     

Stability of benzoporphyrin photosensitizers in water/ethanol mixtures: pKa determination and self‐aggregation processes

Benzoporphyrin monoacid derivatives, here named B3A and B3B, are promising new drugs for photodynamic therapy. Although both isomers show interesting characteristics as photosensitizing compounds, they have some distinct physicochemical properties such as the tendency to self‐aggregate in water‐rich media. Because pH drives the presence of each species, the pK_a of these compounds assumes strategic importance. However, traditional micro‐titration methods and UV–Vis absorption techniques fail to give reliable pK_a values due to the characteristics of this highly complex system, such as the precipitation of hydrophobic species, close pK_a values, and high absorption band superposition. In the present work, chemometric tools are employed to evaluate pK_a, and the kinetic tendency of monomers to undergo self‐aggregation is investigated. In solvent mixtures at low water percentage in ethanol, both B3A and B3B are stabilized in a monomeric state. However, in mixtures with a high water content, self‐aggregation takes place, mainly under a mild pH acid condition (3 < pH < 6), in which the prevalent protolytic species of both isomers is the neutral charged form, compounds with carboxylic and porphyrin free‐base groups. It is demonstrated that both isomers can undergo aggregation following a self‐catalytic mechanism, which is 2000 times slower to B3A than B3B. For B3A, the aggregation is manifested by a decrease in the monomer band with the aggregation band probably superposed to that of the monomer. For B3B, together with the decrease in the monomer band, a new band related to self‐aggregates is observed. Copyright © 2010 John Wiley & Sons, Ltd.     

A gradient-enhanced continuum damage model for fibre-reinforced materials at finite strains

The assumption of purely local continuum damage formulations may imply a loss of well-posedness of the underlying boundary value problem. With regard to numerical methods such as the finite element method, this may lead to mesh-dependent solutions, a vanishing localised damage zone upon mesh refinement, and hence physically questionable results. In order to circumvent these deficiencies, i.e. to regularise the problem, we, in this contribution, apply a non-local gradient-based damage formulation within a geometrically non-linear setting allowing for large deformations. (© 2014 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim)     

Classical ionization for the aperiodic driven hydrogen atom

The classical ionization rate, for 1D hydrogen atom under intense field, was obtained for several almost-periodic (with different degrees of randomness) and random possibilities for the electric field amplitude; it was observed that the less effective is the ionization due to an amplitude sequence for weak intensity, the more effective it is for strong fields. Most numerical calculations were performed with simple adaptations of the Kepler map, which were supported by Hamiltonian calculations.     

Optimizing the Electrocatalytic Activity of Surface Confined Co Macrocyclics for the Electrooxidation of Thiocyanate at pH 4

We have studied the trends in catalytic activity of several Co macrocyclics confined on the surface graphite electrodes for the oxidation of thiocyanate. A plot of log i (at constant E) versus the formal potential of the catalyst gives a volcano correlation, indicating that the Co(II/I) redox potential needs to be tuned, in order to achieve maximum reactivity. Graphite electrodes modified with Co phthalocyanine at pH 4 exhibit linear amperometric response for thiocyanate concentration in the range 10^?7 and 10^?3 M. Theoretical calculations show that electrocatalytic activity (as log i at constant E) plotted versus the energy of the LUMO of the Co complex also gives a volcano correlation.     

Simple LC–MS Determination of Citric and Malic Acids in Fruits and Vegetables

A rapid, reliable and sensitive method has been developed to determine malic and citric acid in fruits and vegetables. The methodology is based on simple extraction with an aqueous solution of ethanol (80% v/v) and subsequent chromatographic analysis by liquid chromatography coupled to mass spectrometry. Electrospray ionization in negative mode was used. The best response for citric and malic acid was provided by molecular ions [M?H]^? at m/z 191 and 133 respectively. These ions were used for quantification, whereas other fragments were used as confirmation ions. Different variables involved in the separation and detection process, such as mobile phase, gradient profile and flow rate have been optimised. Linearity, repeatability, recovery and limits of quantification were evaluated. Good linearity was obtained up to 5,000 mg kg^?1. Recovery ranged from 90.0 to 104.6%, repeatability (expressed as RSD) was <8% for tested matrices, and limits of quantification were equal or lower than 65 mg kg^?1. Finally, the method was applied to the analysis of samples of orange, tomato and pepper.     

Radical of submodules and symmetric algebra

A prime ideal of the symmetric algebra of an R-module N is associated to every prime submodule M ?N and this assignment is then used to obtain a new characterization of the radical of a submodule. Several applications of these results are also included.