Solid phase microextraction (SPME) applied to honey quality control

The assessment of the botanical origin of unifloral honeys is an important application in food control. The current official methods mainly use pollen analysis. The aim of this paper is to present an SPME analytical approach to the study of honey volatiles. Honey samples (40) obtained from hive sites in different regions of Italy were analysed. The samples had six different botanical origins: citrus (five), chestnut (10), eucalyptus (eight), lime tree (11), thyme (two) and dandelion (four). Melissopalynological analysis was also performed. Identification of volatile compounds was carried out by SPME/GC/MS analysis, and quantitative evaluation was done by SPME/GC/FID analysis for compounds with well‐resolved peaks. Using the SPME method, all samples with the same botanical origin gave remarkably similar GC profiles. Some volatile compounds were found only in specific floral source honey samples and thus could be interesting for use as markers. Copyright © 2003 Society of Chemical Industry     

Impact of synthesis conditions on the structure and performance of Li2FeSiO4

Three different synthesis techniques (hydrothermal synthesis, modified Pechini synthesis and Pechini synthesis) were successfully used for preparation of Li₂FeSiO₄ samples. The obtained samples possess some differences in the morphology and in the particle size, as well as in the presence of in situ formed carbon. The best electrochemical performance has been obtained with the smallest particles embedded into carbon matrix. Such a Li₂FeSiO₄/C composite contains the highest amounts of impurities (Fe₂O₃, SiO₂ and Li₂SiO₃) and only 68.8 at.% of iron is in the form of Fe^II as detected by Mössbauer spectroscopy, respectively. Despite the highest amount of impurities, the sample shows the highest reversible capacity (approximately 100 mAh g⁻¹ based on whole silicate-derived material). With the proper structuring of Li₂FeSiO₄/C composites, utilisation of large part of capacity is also possible at current densities corresponding to C/5 and C/2 cycling rate. A lower amount of impurities was found in the samples that do not contain any in situ carbon after synthesis. Among them, the highest purity is possessed by the sample prepared at 900 °C, as determined using Mössbauer spectroscopy. The results obtained by Mössbauer spectroscopy and XRD analysis indicate on the differences in the crystal structure between the thermally treated samples and the sample prepared by hydrothermal synthesis.     

Embedded Multicore Processors and Systems

Unlike desktop PC or server applications, multicore devices used in embedded systems are many and diverse. There are many potential approaches to solving the numerous multicore-related issues. The articles in this issue on embedded multicore processors and systems represent a small sampling of these issues.     

Image restoration in chirp-pulse microwave CT (CP-MCT)

Chirp-pulse microwave computed tomography (CP-MCT) is a technique for imaging the distribution of temperature variations inside biological tissues. Even if resolution and contrast are adequate to this purpose, a further improvement of image quality is desirable. In this paper, we discuss the blur of CP-MCT images and we propose a method for estimating the corresponding point spread function (PSF). To this purpose we use both a measured and a computed projection of a cylindrical phantom. We find a good agreement between the two cases. Finally the estimated PSF is used for deconvolving data corresponding to various kinds of cylindrical phantoms. We use an iterative nonlinear deconvolution method which assures nonnegative solutions and we demonstrate the improvement of image quality which can be obtained in such a way.     

A solid-phase microextraction device for the analysis of electrochemical reaction products by gas chromatography/mass spectrometry

Presented is a solid-phase microextraction syringe-electrode assembly that may be used to identify electrode reaction products. After an electrochemical experiment, the electrode within this syringe-electrode assembly can be introduced into the injection port of a gas chromatograph. Electrochemical reaction products can be analyzed, provided they adhere to the electrode surface and are amenable to gas chromatographic/mass spectrometric analysis. We highlight the potential usefulness of this device using well-known electrochemical reaction of quinones.