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71.
72.
R. J. C. Lima E. C. Santos-Junior A. J. D. Moreno P. F. Façanha-Filho P. T. C. Freire M. I. Yoshida 《Journal of Thermal Analysis and Calorimetry》2013,111(1):627-631
In this study l-alanine, l-threonine, and taurine crystals were characterized through dilatometric technique and thermogravimetric and differential thermal analysis. The dilatometric analysis shows that the thermal expansion of the crystals is correlated with the strengths of local hydrogen bonding in the amino acid structures at room temperature. Thermogravimetric analysis and differential thermal analysis of the l-alanine, taurine, and l-threonine crystals have been performed at high temperatures. No clear correlation between the hydrogen bonding strengths and endothermic peak positions was observed. 相似文献
73.
A. Bonesi M. Asteazaran M. S. Moreno G. Zampieri S. Bengio W. Triaca A. M. Castro Luna 《Journal of Solid State Electrochemistry》2013,17(7):1823-1829
Supported PtSnIr/C, PtSn/C, and IrSn/C catalysts with potential application in a direct alcohol fuel cell were prepared by chemical reduction employing Pechini methodology. The catalyst particles were characterized by high-resolution transmission electron microscopy, energy-dispersive X-ray spectroscopy, and X-ray photoelectron spectroscopy (XPS). Linear sweep voltammetry (LV), chronoamperometry, and electrochemical impedance spectroscopy (EIS) measurements were performed by using a glassy carbon working electrode covered with the catalyst in a 1 M ethanol?+?0.5 M H2SO4 solution at 60 °C. It was demonstrated through XPS that PtSnIr/C and IrSn/C contain both IrO2 and SnO2. LV and chronoamperometry show a better catalytic behavior for ethanol oxidation on PtSnIr/C in the low-potential region and the improvement is attributed to the presence of both Sn and Ir oxides. The EIS accurately established that PtSnIr/C improved ethanol oxidation at lower potentials than PtSn/C. 相似文献
74.
Alexandre Zagdoun Dr. Aaron J. Rossini Dr. Matthew P. Conley Wolfram R. Grüning Martin Schwarzwälder Dr. Moreno Lelli Dr. W. Trent Franks Prof. Dr. Hartmut Oschkinat Prof. Dr. Christophe Copéret Prof. Dr. Lyndon Emsley Dr. Anne Lesage 《Angewandte Chemie (International ed. in English)》2013,52(4):1222-1225
75.
B. M. da Fonseca I. E. D. Moreno M. Barroso S. Costa J. A. Queiroz E. Gallardo 《Analytical and bioanalytical chemistry》2013,405(12):3953-3963
A method using microextraction by packed sorbent (MEPS) and gas chromatography–tandem mass spectrometry (GC-MS/MS) is described for the determination of seven antipsychotic drugs in human plasma. The studied compounds were chlorpromazine (CPZ), haloperidol (HAL), cyamemazine, quetiapine, clozapine, olanzapine (OLZ), and levomepromazine; promazine, protriptyline, and deuterated CPZ were used as internal standards. The validation parameters included selectivity, linearity and limits of detection and quantitation, intra- and interday precision and trueness, recovery, and stability and were studied according to internationally accepted guidelines. The method was found to be linear between the lower limit of quantitation and 1000 ng/mL, except for OLZ and HAL (200 ng/mL), with determination coefficients higher than 0.99 for all analytes, and extraction efficiencies ranged from 62 to 92 %. Intra- and interday precision ranged from 0.24 to 10.67 %, while trueness was within a ±15 % interval from the nominal concentration for all analytes at all studied levels. MEPS has shown to be a rapid procedure for the determination of the selected antipsychotic drugs in human plasma, allowing reducing the handling time and the costs of analysis. Furthermore, GC-MS/MS has demonstrated to be a powerful tool for the simultaneous quantitation of the studied compounds, enabling obtaining adequate selectivity and sensitivity using a sample volume of as low as 0.25 mL. 相似文献
76.
Alain Chaintreau Wolfgang Fieber Horst Sommer Alexis Gilbert Keita Yamada Naohiro Yoshida Alain Pagelot Detlef Moskau Aitor Moreno Jürgen Schleucher Fabiano Reniero Margaret Holland Claude Guillou Virginie Silvestre Serge Akoka Gérald S. Remaud 《Analytica chimica acta》2013
Isotopic 13C NMR spectrometry, which is able to measure intra-molecular 13C composition, is of emerging demand because of the new information provided by the 13C site-specific content of a given molecule. A systematic evaluation of instrumental behaviour is of importance to envisage isotopic 13C NMR as a routine tool. This paper describes the first collaborative study of intra-molecular 13C composition by NMR. The main goals of the ring test were to establish intra- and inter-variability of the spectrometer response. Eight instruments with different configuration were retained for the exercise on the basis of a qualification test. Reproducibility at the natural abundance of isotopic 13C NMR was then assessed on vanillin from three different origins associated with specific δ13Ci profiles. The standard deviation was, on average, between 0.9 and 1.2‰ for intra-variability. The highest standard deviation for inter-variability was 2.1‰. This is significantly higher than the internal precision but could be considered good in respect of a first ring test on a new analytical method. The standard deviation of δ13Ci in vanillin was not homogeneous over the eight carbons, with no trend either for the carbon position or for the configuration of the spectrometer. However, since the repeatability for each instrument was satisfactory, correction factors for each carbon in vanillin could be calculated to harmonize the results. 相似文献
77.
Ulrich Aschauer Olga Burgos-Montes Rodrigo Moreno Paul Bowen 《Journal of Dispersion Science and Technology》2013,34(4):470-479
For modern processing of ceramics at the nanoscale, the influence of interparticle interactions in the suspended state becomes increasingly important. The Hamaker 2 program has been developed for the rapid prediction of these interactions, allowing us to gain important understanding of the often delicate balance of forces in ceramic powder suspensions. This article discusses the theoretical foundation of the implemented models and shows the benefit of this predictive approach applied to mullite production by colloidal methods. 相似文献
78.
M. Eugenia Pérez‐Ojeda Dr. Beatriz Trastoy Álvaro Rol Dr. María D. Chiara Prof. Dr. Inmaculada García‐Moreno Dr. Jose Luis Chiara 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(21):6630-6640
A general procedure for the assembly of hetero‐bifunctional cubic silsesquioxanes with diverse functionality and a perfectly controlled distribution of functional groups on the inorganic framework has been developed. The method is based on a two‐step sequence of mono‐ and hepta‐functionalization through the ligand‐accelerated copper(I)‐catalyzed azide–alkyne cycloaddition of a readily available octaazido cubic silsesquioxane. The stoichiometry of the reactants and the law of binomial distribution essentially determine the selectivity of the key monofunctionalization reaction when a copper catalyst with strong donor ligands is used. The methodology has been applied to the preparation of a set of bifunctional nano‐building‐blocks with orthogonal reactivity for the controlled assembly of precisely defined hybrid nanomaterials and a fluorescent multivalent probe for application in targeted cell‐imaging. The inorganic cage provides an improved photostability to the covalently attached dye as well as a convenient framework for the 3D multivalent display of the pendant epitopes. Thus, fluorescent bioprobes based on well‐defined cubic silsesquioxanes offer interesting advantages over more conventional fully organic analogues and ill‐defined hybrid nanoparticles and promise to become powerful tools for the study of cell biology and for biomedical applications. 相似文献
79.
Ionic liquids as stationary phases in gas chromatography: Determination of chlorobenzenes in soils
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Rosa María González Paredes Carmelo García Pinto José Luis Pérez Pavón Bernardo Moreno Cordero 《Journal of separation science》2014,37(12):1448-1455
The present research focuses on the evaluation of different ionic liquid (IL) stationary phases in gas chromatography. The different IL columns were evaluated in terms of peak resolution (Rs) and peak symmetry for the separation of the chlorobenzenes. The determination of chlorobenzenes in soil samples by means of the optimal IL stationary phase (SLB‐IL82) is proposed as an application. Soil pretreatment was based on a simplified quick, easy, cheap, effective, rugged, and safe extraction procedure and a large injection volume via a programed temperature vaporizer working in solvent vent mode. The retention time of the chlorobenzenes increased as the polarity of the IL column decreased. SLB‐IL82 is the stationary phase that provides the best values as regards Rs and asymmetry factor. Soil sample blanks were spiked with the analytes before subjecting the sample to the extraction process. The existence of a matrix effect was checked and the analytical characteristics of the method were determined in a fortified garden soil sample. The method provided good linearity, good repeatability and reproducibility values, and the LODs were in the 0.1–4.7 μg/kg range. Two fortified soil samples were applied to validate the proposed methodology. 相似文献
80.
Victoria Mánuel Juan J. Pinto Carolina Mendiguchía Carlos Moreno 《Central European Journal of Chemistry》2014,12(3):348-353
In this work, Cd(II) extraction in natural waters by organophosphorus extractants as organic phase, as well as its back-extraction in an acidic media, has been studied. Cadmium extraction behavior at natural waters’ pH conditions (values in the range 7–8) was studied with two different extractants and co-ions, obtaining the highest extraction efficiency when using 0.1M Cyanex 272 in kerosene as organic phase and 0.1 M NO3 ? as co-ion. Once they were selected, the effect on the extraction efficiency of sample pH, buffer concentration, extraction time, Cyanex 272 concentration as well as back-extractant concentration, was studied. The presence of the main inorganic and organic ligands in the sample was also studied, observing that extraction efficiency was affected most significantly when chlorides were present, with a decrease of about 14%, proving negligible for the others. Under the selected conditions, spiked real samples were successfully analyzed. 相似文献