Acrylic-urethane/modified Rhodamine-B eco-friendly UV-curable anticounterfeiting ink

Counterfeiting is an ever-growing global problem challenging companies, governments, and customers. In recent decades, as a potential remedy, anticounterfeiting technology and information security have gained a great deal of attention from academia and industry. In this work and for the first time, Rhodamine B (RhB), an efficient and enticing fluorescent material, was modified and used as a reactive stimuli-responsive component in the formulation of an eco-friendly ink. Additionally, a UV-curable polyurethane dispersion (UCPUD) with zero volatile organic compound was synthesized and employed as the matrix for the fluorescent ink. The modified RhB and UCPUD were thoroughly characterized using Fourier-transform infrared and proton nuclear magnetic resonance analyses. Exploiting the fluorescent monomer in the ink formulations could enhance the absorption intensity (λ_max = 552 nm) of the prepared ink up to 7 with respect to its solution (λ_max = 519 nm). The printed pattern was immediately illuminated with brilliant red-pink fluorescence emission upon UV irradiation. It has been shown that the prepared fluorescent ink has potential applications in the encryption, security marking, and optical authentication of confidential cellulose substrates.     

Temperature-induced dispersive solid-phase extraction as a new approach for preconcentration of Sudan dyes in water and food samples prior to the determination by high-performance liquid chromatography

This study introduced a new microextraction method named temperature-induced dispersive solid-phase extraction. The performance of the method was demonstrated with the determination of Sudan dyes in food and natural water samples. In this method, a low quantity of sorbent was added to the aqueous solution and the mixture was shaken manually for about one minute. Then, the solution was heated in an ultrasonic water bath, and the sorbent was dissolved. Subsequently, the solution was cooled down with ice water, and consequently, the solubility of the sorbent was reduced in the sample solution and became cloudy. The phase separation was accelerated by centrifugation. The upper liquid phase was picked up using a syringe, and the remainder was solved in methanol and introduced into the HPLC for analysis. Various parameters affecting the extraction yield were evaluated. Analytical parameters, including limits of detection (0.011–0.016 μg/L) and quantification (0.038–0.055 μg/L), relative standard deviations (2.3%–3.1%), and preconcentration factor (40) proved the high efficiency of the developed method for the analysis of Sudan dyes. The proposed method was used to measure Sudan dyes in water and food samples and showed good extraction recoveries (95.0%–103.5%).     

Electron-transfer reduction of dinuclear copper peroxo and bis-μ-oxo complexes leading to the catalytic four-electron reduction of dioxygen to water

The four-electron reduction of dioxygen by decamethylferrocene (Fc*) to water is efficiently catalyzed by a binuclear copper(II) complex (1) and a mononuclear copper(II) complex (2) in the presence of trifluoroacetic acid in acetone at 298 K. Fast electron transfer from Fc* to 1 and 2 affords the corresponding Cu(I) complexes, which react at low temperature (193 K) with dioxygen to afford the η(2):η(2)-peroxo dicopper(II) (3) and bis-μ-oxo dicopper(III) (4) intermediates, respectively. The rate constants for electron transfer from Fc* and octamethylferrocene (Me(8)Fc) to 1 as well as electron transfer from Fc* and Me(8)Fc to 3 were determined at various temperatures, leading to activation enthalpies and entropies. The activation entropies of electron transfer from Fc* and Me(8)Fc to 1 were determined to be close to zero, as expected for outer-sphere electron-transfer reactions without formation of any intermediates. For electron transfer from Fc* and Me(8)Fc to 3, the activation entropies were also found to be close to zero. Such agreement indicates that the η(2):η(2)-peroxo complex (3) is directly reduced by Fc* rather than via the conversion to the corresponding bis-μ-oxo complex, followed by the electron-transfer reduction by Fc* leading to the four-electron reduction of dioxygen to water. The bis-μ-oxo species (4) is reduced by Fc* with a much faster rate than the η(2):η(2)-peroxo complex (3), but this also leads to the four-electron reduction of dioxygen to water.     

Synthesis of Nickel Oxide Nanoparticles from Thermal Decomposition of a New Precursor

Nickel oxide nanoparticles (25 nm) have been synthesized via decomposition of a new precursor nickel octanoate Ni(octa)₂ in the presence of oleylamine (C₁₈H₃₇N) and triphenylphosphine (C₁₈H₁₅P), in mild conditions. To control the particle size and morphology, combination of C₁₈H₁₅P and C₁₈H₃₇N were applied as surfactants. In this process, oleylamine was used as both the medium and the stabilizing reagent. C₁₈H₃₇N and C₁₈H₁₅P play an important role in preventing aggregation of NiO nanoparticles. The products were characterized by XRD, SEM, TEM, FT–IR, and TGA.     

Copper Supported on the SiO2 Nanoparticle in Click Chemistry: An Alternative Catalytic System for Regioselective and One‐Pot Synthesis of 1,2,3‐Triazoles and β‐Hydroxytriazoles

In this work, readily prepared copper supported on the SiO₂ nanoparticles has been found to effectively catalyze the 1,3‐dipolar cycloaddition of a variety of azides, alkynes, epoxides and sodium azide, furnishing the corresponding 1,2,3‐triazoles and β‐hydroxytriazoles. Click reaction proceeds in short reaction times and under mild reaction conditions, and the resulting products are obtained in good yields at ambient temperature.     

A QXP-based multistep docking procedure for accurate prediction of protein-ligand complexes

The two great challenges of the docking process are the prediction of ligand poses in a protein binding site and the scoring of the docked poses. Ligands that are composed of extended chains in their molecular structure display the most difficulties, predominantly because of the torsional flexibility. On the basis of the molecular docking program QXP-Flo+0802, we have developed a procedure particularly for ligands with a high degree of rotational freedom that allows the accurate prediction of the orientation and conformation of ligands in protein binding sites. Starting from an initial full Monte Carlo docking experiment, this was achieved by performing a series of successive multistep docking runs using a local Monte Carlo search with a restricted rotational angle, by which the conformational search space is limited. The method was established by using a highly flexible acetylcholinesterase inhibitor and has been applied to a number of challenging protein-ligand complexes known from the literature.     

Dynamical thermal effects in InGaAsP microtubes at telecom wavelengths

We report on the observation of a dynamical thermal effect in InGaAsP microtubes at telecom wavelengths. The microtubes are fabricated by releasing a strained semiconductor bilayer and are picked up by abruptly tapered optical fibers for subsequent coupling with adiabatically tapered optical fibers. As a result of absorption by InAs quantum dots embedded in the tube structure, these microtubes show dynamical thermal effects at wavelengths around 1525 nm and 1578 nm, while they are passive at longer wavelengths near 1634 nm. The photon absorption induced thermal effect is visualized by generating a pair of microbottles. The dynamical thermal effect can be avoided or exploited for passive or active applications by utilizing appropriate resonance wavelengths.     

Numerical investigation of heat transport and fluid flow during the seeding process of oxide Czochralski crystal growth Part 2: rotating seed

In this paper, the role of seed rotation on the characteristics of the two‐dimensional temperature and flow field in the oxide Czochralski crystal growth system has been studied numerically for the seeding process. Based on the finite element method, a set of two‐dimensional quasi‐steady state numerical simulations were carried out to analyze the seed‐melt interface shape and heat transfer mechanism in a Czochralski furnace with different seed rotation rates: ω_seed = 5‐30 rpm. The results presented here demonstrate the important role played by the seed rotation for influencing the shape of the seed‐melt interface during the seeding process. The seed‐melt interface shape is quite sensitive to the convective heat transfer in the melt and gaseous domain. When the local flow close to the seed‐melt interface is formed mainly due to the natural convection and the Marangoni effect, the interface becomes convex towards the melt. When the local flow under the seed‐melt interface is of forced convection flow type (seed rotation), the interface becomes more concave towards the melt as the seed rotation rate (ω_seed) is increased. A linear variation of the interface deflection with respect to the seed rotation rate has been found, too. (© 2007 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Growth of KCl crystal by Czochralski method and influence of nanodiamond impurity on its hardness and optical properties

KCl alkali halide crystal with different nanodiamond impurity was grown by Czochralski method. X‐Ray diffraction of the outcome samples reveals that they are still single crystal. Also crystal hardness observation reveals that the hardness of KCl single crystal has been increased by adding different percentage of nanodiamond impurity. In addition, the study of FTIR spectrums of the pure and doped crystals represents that the KCl optical properties has not changed.