Interaction of colloidal particles of NH(4)(+)-montmorillonite with activated carbon

The interaction between negative colloidal particles of NH(4)(+)-montmorillonite and particles of activated carbon was studied as a function of particle concentration, pH, and time of contact. The results show that carbon particles act as a support/bridge for clay particles, the type of resulting clay/carbon/clay associations depending on the pH and the clay/carbon ratio in the system. The relation between clay and carbon particles can be described by equations of the Langmuir type. For the same carbon particle concentration in the system, the relation varies from 6820 to 36,100 and is dependent on pH. The interaction coefficients at pH 6.5 correspond to reaction of pseudo-first (k(1)=4.14 x 10(-3) to 1.93 x 10(-3) s(-1)) and pseudo-second order (k(2)=9.36 x 10(-14) to 2.47 x 10(-14) cm(3)s(-1)) for different clay/carbon ratios. By using the Dubinin-Radushkevich equation, the interaction energy (+/-22.42, +/-685.0, and +/-14.63 J mol(-1)) was obtained for three different pH values (5, 6.7, and 7.6), demonstrating that the reaction is mainly physical.     

Study of nanocrystalline BiMnO3-PbTiO3: synthesis, structural elucidation, and magnetic characterization of the whole solid solution

In the last ten years, the study and the search for new multiferroic materials have been a major challenge due to their potential applications in electronic technology. In this way, bismuth-containing perovskites (BiMO(3)), and particularly those in which the metal?M position is occupied by a magnetically active cation, have been extensively investigated as possible multiferroic materials. From the point of view of synthesis, only a few of the possible bismuth-containing perovskites can be prepared by conventional methods but at high pressures. Herein, the preparation of one of these potential multiferroic systems, the solid solution xBiMnO(3)-(1-x)PbTiO(3) by mechanosynthesis is reported. Note that this synthetic method allows the oxides with high x values, and more particularly the BiMnO(3) phase, to be obtained as nanocrystalline phases, in a single step and at room temperature without the application of external pressure. These results confirm that, in the case of Bi perovskites, mechanosynthesis is a good alternative to high-pressure synthesis. These materials have been studied from the point of view of their structural characteristics by precession electron diffraction and magnetic property measurements.     

Development of headspace SPME method for analysis of volatile organic compounds present in human biological specimens

In recent years, interest has increased regarding the identification of volatile organic compounds (VOCs) for metabolic profiling, human scent identification of the living and deceased, and diagnostic potentials for certain diseases that are known for its association with distinct odor. In this study, a method has been developed that is capable of sampling, identifying, and differentiating the VOCs present in various biological specimens of forensic importance (blood, breath, buccal cells, and urine) taken from the same individuals. The developed method requires a pretreatment step to remove targeted VOCs from the sampling apparatus prior to sampling of the individual specimens. The VOCs collected from the biological specimens were characterized by solid-phase microextraction and gas chromatography/mass spectrometry with ratios of the most abundant and frequent VOCs compared using qualitative and semiquantitative methods. Blood, breath, and buccal cells required extraction procedures ranging from 18 to 21 h in order to optimize the limit of detection, which averaged 5–15 ng across these specimens. The optimal method for measuring urine VOCs was complete in less than an hour; however, the limit of detection was higher with a range of 10–40 ng quantifiable. The demonstrated sensitivity and reproducibility of the methods developed allow for population studies of human scent VOCs from various biological specimen collection kits used in the forensic and clinical fields.     

The water/graphitic-carbon interaction energy

The water/graphitic-carbon interaction energy was obtained for a sample having a water surface site adsorption density of 13.3 μmol m⁻². The interaction energy was determined from the spreading pressure of water, its surface tension and the water contact angle and using a formula obtained by the combination of the Young equation with a general equation of pair interaction. The values obtained for contact angles 42° and 86° are 7.63 and 7.18 kJ mol⁻¹ of water are similar to the water binding energies obtained from molecular dynamic simulations of water droplets on a graphite surface: 6.7-8.33 kJ mol⁻¹.     

Synthesis of biodegradable conjugated polymers with controlled backbone flexibility

A series of flexible, highly bright fluorescent poly(p‐phenyleneethynylene)s (PPEs) was prepared by employing a disulfide containing nonconjugated monomer at various ratios under Sonogashira reaction conditions. PPEs with flexible linkers exhibited fluorescence properties comparable to those of a fully conjugated PPE when less than 50% of flexible monomers were incorporated into the backbone. To evaluate the self‐assembly properties of PPEs, a series of conjugated polymer nanoparticles (CPNs) was fabricated by treating PPEs with organic acids followed by dialysis. CPNs containing linkers exhibited different complexation behavior with polysaccharides, warranting further investigation into how flexibility and biodegradability of CPNs influence their cellular interaction and entry. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2015 , 53, 1403–1412     

Conjugated polymer nanoparticles for small interfering RNA delivery

Loosely aggregated conjugated polymer nanoparticles (CPNs) were used as nontoxic and efficient small interfering RNA (siRNA) delivery vehicles with delivery visualization. A significant down regulation (94%) of a target gene was achieved by transfection of HeLa cells with the CPNs/siRNA complexes, supporting CPN as a promising siRNA delivery carrier.     

Transversality condition for singular infinite horizon calculus of variations

We consider an optimal infinite horizon calculus of variations problem linear with respect to the velocities. In this framework the Euler–Lagrange equation are known to be algebraic and thus no informative for the general optimal solutions. We prove that the value of the objective along the MRAPs, the curves that connect as quickly as possible the solutions of the Euler–Lagrange equation, is Lipschitz continuous and satisfies a Hamilton–Jacobi equation in some generalised sense. We derive then a sufficient condition for a MRAP to be optimal by using a transversality condition at infinity that we generalize to our non regular context.     

Controlled aggregation in conjugated polymer nanoparticles via organic acid treatments

Understanding and controlling aggregation structures of conjugated polymers (CPs) in aqueous solutions is critical to improving the physical and photophysical properties of CPs for biological applications. Here, we present spectroscopic evidence, including nuclear magnetic resonance (NMR) spectroscopic results, that different organic acid treatment induces different aggregation structures and photophysical properties of CPs in water. Conjugated polymer nanoparticles (CPNs) were fabricated by treating a non-aqueous soluble, primary amine-containing poly(phenylene ethynylene) (PPE-NH(2)) with organic acids followed by dialysis. CPNs formed by acetic acid (AA) treatment (CPN-AAs) exhibit characteristics of loose aggregation with minimal π-π stacking, while CPNs formed by tartaric acid (TA) treatment (CPN-TAs) exhibit a high degree of π-π stacking among PPE-NH(2) chains. The controlled aggregation for a specific application was demonstrated by comparing the fluorescence quenching abilities of the CPN-AAs and the CPN-TAs. A doubled Stern-Volmer constant was obtained from the densely packed CPN-TAs compared to that of the loosely aggregated CPN-AAs.