Aplicación del método level set para modelar el proceso de combustión premezclada en un motor Otto de dos tiempos

In this paper, the numerical method level set has been used to model the combustion process in an Otto two-stroke engine. The level set has been implemented in a CFD (Computational Fluid Dynamics) software based in finite volumes. The pressure and temperature fields have been obtained, such as the propagation of the flame front. In order to validate this model, the numerically obtained results have been compared with experimental data, verifying a satisfactory concordance between both of them. Besides, the level set method has been compared with other numerical procedure, showing the difference between both results.     

Development of a method based on sorbent trapping followed by solid-phase microextraction for the determination of synthetic musks in indoor air

Synthetic musks are extensively used as fragrance components in a wide range of consumer and personal care products such as detergents, shampoos, perfumes and other cosmetic products. Amongst them, galaxolide and tonalide have become ubiquitous pollutants due to their continuous releasing into the environment. Because of their nature as artificial fragrances, inhalation should be considered as an important exposure pathway, especially in indoor environments. However, up to now very few studies have been carried out to determine these emergent pollutants indoors. In this work, a simple and highly sensitive methodology for the analysis of synthetic musk fragrances in indoor air samples is presented. The proposed methodology combines solid-phase extraction (SPE) and solid-phase microextraction (SPME), followed by gas chromatography-mass spectrometry (GC/MS). To the best of our knowledge, this is the first method based on SPME for the analysis of musks in air. By active sampling, musks present in air were adsorbed onto 25mg Tenax and then transferred to a SPME fiber in the headspace mode (HS). An experimental design strategy was used to optimize main factors potentially affecting the microextraction process such as fiber coating, temperature and the addition of a microvolume of organic solvent to the solid sorbent prior to SPME. Breakthrough of the SPE sorbent was studied from 1 to 10m(3) without significant losses. Recovery studies were performed at two concentration levels (2 and 20ngm(-3)), obtaining quantitative recoveries (>/=85%) by external calibration. A comprehensive study was performed in order to estimate the limits of detection taking into account the contamination risks and laboratory blanks. Values at the sub ngm(-3) level were achieved for all the target compounds sampling 5m(3) air. External calibration, not requiring the complete sampling process, demonstrated to be suitable for the quantification of all musk compounds. Finally, several indoor environments were analyzed using the proposed method.     

Determination of dimethyl fumarate in desiccant and mouldproof agents using ultrasound-assisted extraction gas chromatography with electron-capture detection

A fast, simple, low cost, and high throughput method has been developed for the determination of dimethyl fumarate (DMF) in desiccant and anti-mould agents employed for protecting clothes, footwear and accessories from humidity and mould. The procedure is based on ultrasound-assisted extraction followed by GC-μECD analysis. The method was conveniently optimized, and the analyte was efficiently extracted from the samples in only 5 min using such a low volume of solvent (ethyl acetate) as 1 mL. Simultaneous extractions could be carried out in also 5 min without loosing efficiency. The method has been validated showing good linearity and selectivity. Precision was satisfactory with RSD of 4–5%. Recovery was evaluated in two real samples at different DMF concentration levels and was >90% in all cases. Limit of detection and quantification were at the ng g⁻¹ level. The proposed procedure was applied to the determination of DMF in several desiccant and anti-mould samples. Although most of them were labelled as “silica gel” all the samples tested with the exception of three presented important amounts of DMF, many of them at the high μg g⁻¹ level. The presence and the high concentrations of this allergenic fungicide in desiccant and anti-mould sachets employed in many consumer products, such as clothes and footwear, should be a matter of concern.     

Optimisation of laser removal of biological crusts in granites

Laser cleaning of stones is a well established technique in the field of cultural heritage; however, there are few studies concerning its application to granites, though these rocks have been used from the past as structural and ornamental material in public works and buildings. In humid climates granite is almost permanently damp which causes biological colonisation and blackening of exterior surfaces. This work was focussed on the removal of biological black crust in granite by means of a Nd:YVO4 laser at the wavelength of 355 nm. Analysis of the conditions for efficient removal, and evaluation of the morphological/textural changes on the stone surface allowed us to establish safe conditions of irradiation. A number of surface analytical techniques such as optical microscopy (OM), optical profilometry, scanning electron microscopy/energy dispersive X-ray spectrometry (SEM/EDX) and X-ray photoelectron spectroscopy (XPS) were used to asses the effects of the laser treatment.     

Electric field controlled g-factor in parabolic well determined by transport measurements

The Shubnikov de Haas oscillations in parabolic well are studied in the tilted magnetic field. The electric field displaces the electron wave function along Z-axis and leads to the strong variation of the average bare g-factor in such system. From the measurements of the filling factor ν_c at which the spin gap collapse occurs, we deduce the total Zeeman energy, which consists of the bare Zeeman energy and exchange-correlation term. By investigating of the variation of ν_c in tilted field we reliably extract the bare g-factor as a function of the gate voltage.     

Solid-phase microextraction-gas chromatography-mass spectrometry for the analysis of selective serotonin reuptake inhibitors in environmental water

The continuous contamination of surface waters by pharmaceuticals is of most environmental concern. Selective serotonin reuptake inhibitors (SSRIs) are drugs currently prescribed for the treatment of depressions and other psychiatric disorders and then, they are among the pharmaceuticals that can occur in environmental waters. Solid-phase microextraction (SPME) coupled to gas chromatography-mass spectrometry has been applied to the extraction of five SSRIs--venlafaxine, fluvoxamine, fluoxetine, citalopram and sertraline--from water samples. Some of the analytes were not efficiently extracted as underivatized compounds and so, an in situ acetylation step was introduced in the sample preparation procedure. Different parameters affecting extraction efficiency such as extraction mode, fiber coating and temperature were studied. A mixed-level fractional factorial design was also performed to simultaneously study the influence of other five experimental factors. Finally, a method based on direct SPME at 100 degrees C using polydimethylsiloxane-divinylbenzene fibers is proposed. The performance of the method was evaluated, showing good linearity and precision. The detection limits were in the sub-ng/mL level. Practical applicability was demonstrated through the analysis of real samples. Recoveries obtained for river water and wastewater samples were satisfactory in all cases. An important aspect of the proposed method is that no matrix effects were observed. Two of the target compounds, venlafaxine and citalopram, were detected and quantified in a sewage water sample.     

Emerging Hubs in Plant Light and Temperature Signaling

Due to their nature as sessile organisms, plants must accurately sense their surroundings and then translate this information into efficient acclimation responses to maximize development. Light and temperature are two major stimuli that provide immediate cues regarding energy availability, daylength, proximity of other species and seasonal changes. Both cues are sensed by complex systems and the integration of these signals is of very high value to properly respond to environmental changes without being disguised by random changes. For instance a cold day has a different significance if it occurs during the illuminated phase of the day or during the night, or when days are shortening during the fall instead of a long‐day in spring. Here, we summarize recent advances in the nature of signaling components that operate as connectors of light and temperature signaling, with emphasis on the emerging hubs. Despite the nature of the thermosensors is still in its infancy compared to an important body of knowledge about plant sensory photoreceptors, the interaction of both types of signaling will not only bring clues of how plants integrate environmental information, but also will help in leading research in the nature of the thermosensors themselves.     

Matrix solid-phase dispersion and solid-phase microextraction applied to study the distribution of fenbutatin oxide in grapes and white wine

The fate of the acaricide fenbutatin oxide (FBTO) during the elaboration of white wine is evaluated. Matrix solid-phase dispersion (MSPD) and solid-phase microextraction (SPME) were used as sample preparation techniques applied to the semi-solid and the liquid matrices involved in this research, respectively. Selective determination of FBTO was achieved by gas chromatography with atomic emission detection (GC–AED). GC coupled to mass spectrometry was also used to establish the identity of FBTO by-products detected in must and wine samples. MSPD extractions were accomplished using C18 as dispersant and co-sorbent. Sugars and other polar interferences were first removed with water and water/acetone mixtures, then FBTO was recovered with 8 mL of acetone. When used in combination with GC–AED, the MSPD method provided limits of quantification (LOQs) in the low nanogram per gram range, recoveries around 90% and relative standard deviations below 13% for extractions performed in different days. Performance of SPME for must and wine was mainly controlled by the extraction temperature, time and fibre coating. Under final conditions, FBTO was extracted in the headspace mode for 45 min at 100 °C, using a 100 μm poly(dimethylsiloxane)-coated fibre. The achieved LOQs remained around or below 0.1 ng mL⁻¹, depending on the type of sample, and the inter-day precision ranged from 10% to 13%. FBTO residues in grapes stayed mostly on the skin of the fruit. Although FBTO was not removed during must and white wine elaboration, it remained associated with suspended particles existing in must and lees, settled after must fermentation, with a negligible risk of being transferred to commercialised wine. On the other hand, two by-products of FBTO (bis and mono (2-methyl-2-phenylpropyl) tin) were identified, for first time, in must and final white wines obtained from FBTO treated grapes. Found values for the first species ranged from 0.03 to 0.9 ng mL⁻¹.