Understanding phenol adsorption mechanisms on activated carbons

The interactions between phenol molecules and activated carbons were investigated in order to understand the adsorption mechanism of this aromatic compound. A series of activated carbons with varied chemical composition but similar porous features were synthesized and submitted to phenol exposure from aqueous phase, followed by thermogravimetric analysis and identification of the desorbed species by temperature programmed desorption coupled with mass spectrometry. Based on these experiments, both physi- and chemisorption sites for phenol were identified on the activated carbons. Our results demonstrate that physisorption of phenol depends strictly on the porosity of the activated carbons, whereas chemisorption depends on the availability of the basal planes in the activated carbons. Thus, oxidation of the carbon can suppress the fraction of chemisorbed phenol since the surface functionalities incorporate to the edges of the basal planes; notwithstanding, hydrophilic carbons may present a small but not negligible contribution of chemisorbed phenol depending on the extent of the functionalization. Moreover, these adsorption sites (chemi-) are recovered by simply removal of the surface functionalities after thermal annealing.     

Mössbauer study of iron ore from El Hobo,Huila, Colombia

Iron ore from the El Hobo municipality located in the Huila department in Colombia (2^°35^′7^″N 75^°13^′27^″E) was studied by Mössbauer spectroscopy. The material was quite inhomogeneous, consisting of light brown and dark brown concretions of up to about a centimeter in size, and a sandy fraction. Mössbauer spectra at ambient temperature and at 4.2 K were taken of the two kinds of concretions and the sandy fraction. The concretions contain iron mainly as goethite with only a few percent of hematite. The sandy fraction contains goethite and hematite in roughly equal amounts and a minor fraction of divalent iron that splits magnetically at 4.2 K and may be an impure kind of siderite.     

Dissolving Hydroxyolite: A DNA Molecule into Its Hydroxyapatite Mold

In spite of the clinical importance of hydroxyapatite (HAp), the mechanism that controls its dissolution in acidic environments remains unclear. Knowledge of such a process is highly desirable to provide better understanding of different pathologies, as for example osteoporosis, and of the HAp potential as vehicle for gene delivery to replace damaged DNA. In this work, the mechanism of dissolution in acid conditions of HAp nanoparticles encapsulating double‐stranded DNA has been investigated at the atomistic level using computer simulations. For this purpose, four consecutive (multi‐step) molecular dynamics simulations, involving different temperatures and proton transfer processes, have been carried out. Results are consistent with a polynuclear decalcification mechanism in which proton transfer processes, from the surface to the internal regions of the particle, play a crucial role. In addition, the DNA remains protected by the mineral mold and transferred proton from both temperature and chemicals. These results, which indicate that biomineralization imparts very effective protection to DNA, also have important implications in other biomedical fields, as for example in the design of artificial bones or in the fight against osteoporosis by promoting the fixation of Ca²⁺ ions.     

Optimization of a holographic memory setup using an LCD and a PVA-based photopolymer

Holographic data pages were stored in a polyvinyl alcohol (PVA)/acrylamide (AA) photopolymer. This material is formed of AA photopolymers which are considered interesting materials for recording holographic memories. A liquid crystal device was used to modify the object beam and store the data pages in the material. During the storage process, some parameters like exposure time, beam ratio and reading beam intensity were controlled to obtain high image quality after the reconstruction process. The bit error rate (BER) was calculated fitting the histograms of the images to determine what parameters improve the quality of the images.     

SU(1,1) Coherent States for Position-Dependent Mass Singular Oscillators

The Schr?dinger equation for position-dependent mass singular oscillators is solved by means of the factorization method and point transformations. These systems share their spectrum with the conventional singular oscillator. Ladder operators are constructed to close the su(1,1) Lie algebra and the involved point transformations are shown to preserve the structure of the Barut-Girardello and Perelomov coherent states.     

Thermal diffusivity study of cheese fats by thermal lens detection

In this paper we used thermal lens spectrometry to determine the thermal diffusivity of cheese fats. We have used equal concentrations of cheese fats from oaxaca, chihuahua, gouda, manchego and mozzarella cheeses at 42°C temperature. The two lasers mismatched mode experimental configuration was used with a He-Ne laser, as a probe beam and an Ar⁺ laser as the excitation one. The characteristic time constant of the transient thermal lens was obtained by fitting the theoretical expression to the experimental data in order to obtain the thermal diffusivity of the cheese fat samples. This measured thermal property may contribute to a better understanding of the cheese fats quality, which is very important in food industry.     

First stability eigenvalue characterization of Clifford hypersurfaces

The stability operator of a compact oriented minimal hypersurface is given by , where is the norm of the second fundamental form. Let be the first eigenvalue of and define . In 1968 Simons proved that for any non-equatorial minimal hypersurface . In this paper we will show that only for Clifford hypersurfaces. For minimal surfaces in , let denote the area of and let denote the genus of . We will prove that . Moreover, if is embedded, then we will prove that . If in addition to the embeddeness condition we have that , then we will prove that .