Supercritical fluid extraction and gas chromatography or electroanalysis of metal chelates from different sample matrices

The supercritical fluid extraction of Pb(DDC)2 and MoO2(acac)2 complexes is performed. The previously formed complexes are used in order to simplify the extraction process. In the extraction cell, 9.0 mg of Pb(DDC)2 or 30.0 mg of MoO2(acac)2 is added. With these two complexes, a study of static and dynamic extraction as a function of pressure (1000-2500 psi), temperature (40-160 degrees C), and presence of modifier (methanol) is performed. Under the best conditions, 5.6 mg of Pb(DDC)2 (2.3 mg of Pb2+) is recovered. The parameters are 2500 psi of pressure, 160 degrees C of temperature, 0.5 mL methanol (placed in a 10-mL extraction cell), 60.0 min of static extraction, and 2.0 min of dynamic extraction. It is necessary to add 3.0 mL of methanol to enhance efficiency on the MoO2(acac)2 complex recovery. Quantitative extractions of MoO2(acac)2 (9.0 mg of MoVI) are obtained when the experiments are carried out under 1000-2500 psi of pressure, 140 degrees C, and times no longer than 10.0 min. Then, the study is carried out forming the in situ complexes. For this purpose, metallic ion and ligand are added. Under these conditions, the Pb2+ recovery decreases from 2.3 to 1.9 mg, and the MoVI recovery decreases from 9.0 to 1.0 mg. When 1.9 mg of Pb2+ and 1.0 mg of MoVI or less is placed in the extraction cell, the recoveries are always 100%. The Pb2+ extracts are directly accomplished using gas chromatography-flame ionization detection (GC-FID), and the MoVI extracts are analyzed using GC-FID and catalytic adsorption voltammetry. The quantitation of pure extracts is carried out by constructing calibration curves with complex solutions and sample solutions using the standard addition method. This method is applied by determination of Pb2+ in sodium alginate extracted from algae and blood, urine, and human milk from patients with diagnosed plumbunemy. MoVI is determined in irrigation water and pasture of animal intake.     

Meissner Anisotropy in Deuterated (TMTSF)2Clo4

Both the Meissner-signal (flux expulsion on cooling through T_c) and the shielding signal (obtained by turning on a field in the superconducting state) have been observed in deuterated single crystals for fields oriented both along and normal to the chain axis. A possible isotope effect on T_c is discussed. We find complete diamagnetism in normal fields and incomplete (～ 40 %) diamagnetism in parallel fields. A dramatic drop of the Meissner-effect in parallel fields well below H_c1 is observed and not yet well explained.     

Reductive Ring Opening of Ephedrine and Pseudo-Ephedrine-Derived Oxazolidinium Methiodides by Sodium Borohydride. A Direct Access to New Chiral Amine-Borane Adducts

Sodiun borohydride reacts with oxazolidinium methiodides derived from ephedrine and pseudoephedrine, in ethereal solvents, cleaving regioselectively the C-N bond of the ring and leading, in good yields, to chiral amine-borane adducts of know absolute configuration. The ¹HNMR data allow to predict the most stable conformation.     

Identification of markers of thermal processing (“roasting”) in aqueous extracts of Coffea arabica L. seeds through NMR fingerprinting and chemometrics

Roasting of Coffea arabica L. seeds gives rise to chemical reactions that produce more than 800 compounds, some being responsible for the desired organoleptic properties for which the beverage called “coffee” is known. In the industry, the “roasting profile,” that is, the times and temperatures applied, is key to influence the composition of roasted coffee beans and the flavour of the beverage made from them. The impact of roasting on the chemical composition of coffee has been the subject of numerous studies, including by nuclear magnetic resonance (NMR) spectroscopy. However, the roasting equipment and profiles applied in these studies are often far from real industrial conditions. In this work, the effects of two critical technological parameters of the roasting process, namely, the “development time” (the period of time after the “first crack,” a characteristic noise due to seed disruption) and the final roasting temperature on coffee extracts, were investigated. Seeds were roasted at pilot scale according to 13 industrial roasting profiles and extracted in D₂O. The extracts were analysed by ¹H NMR experiments. The NMR spectra were compared using (a) quantitative analysis of main signals by successive orders of magnitude and (b) chemometric tools (principal component analysis, partial least squares and sparse-orthogonal partial least squares analysis). This allowed to identify compounds, which may serve as markers of roasting and showed that changes in chemical composition can be detected even for slight change in final temperature (~1°C) or in total roasting time (~25 s).     

SULPHENE INTERMEDIATES IN THE SYNTHESIS OF POLY(P-BENZENE-SULPHONAMIDES) AND POLY(P-BENZENE SULPHONATES)

Abstract

Various sulfides are easily oxidized selectively to the corresponding sulfoxides in quantitative yields by iodosylarene (ArIO) catalyzed by metalloporphyrin (TPPM(III)Cl (M [dbnd] Fe, Mn)). The oxidation system is demonstrated to be a possible model for monooxygenase in the study of the stereochemistry of these sulfoxides. Metalloporphyrin-iodosylarene can initially equilibrate with the oxometalloporphyrin (TPPM(V)=O·Cl) formed in situ. The initial process may involve one-electron transfer from the sulfide to the intermediate oxometalloporphyrin followed by coupling of two resulting charged products, and/or nucleophilic attack of sulfide on oxometalloporphyrin oxygen. The overall reactions are depicted by paths with different electron demands from the results of Hammett plots.     

Encagement of Gold Nanoclusters in Crosslinked Resorcinarene Shells

Monolayers of resorcinarene tetraene 1 on gold nanoclusters could be crosslinked by olefin metathesis into a nondesorptive shell. Crosslinking conditions were optimized by monitoring olefin metathesis of 1 by 1 H NMR spectroscopy and obtaining empirical rate constants. Gel permeation chromatography (GPC) was found to be a useful tool for evaluating the enhanced stability of the encaged nanoparticles; resorcinarene-encapsulated nanoparticles which were not subjected to olefin metathesis did not survive GPC analysis, whereas nanoparticles in crosslinked shells were found to be stable.     

Influence of some lime-containing additives on the thermal behavior of urea

Urea is one of the main nitrogen fertilizers used in agriculture. But being well soluble in water, hardly 50% of its nitrogen is assimilated by plants. One possibility to eliminate this disadvantage is to use coating agents for modification of urea to obtain a controlled-realized fertilizer. The aim of this research was to study the influence of different lime-containing additives on the thermal behavior and decomposition kinetics of urea in oxidizing atmosphere. Commercial fertilizer-grade urea (46.4% N) and analytical-grade CaO, MgO, CaCO₃, MgCO₃ were used in the experiments. In addition, one Estonian limestone and one dolomite sample were used as additive or coating material. The experiments with a Setaram Setsys 1750 thermoanalyzer coupled to a Nicolet 380 FTIR Spectrometer by a heated transfer line were carried out under non-isothermal conditions up to 900 °C at the heating rate of 5 °C min^?1 and to calculate kinetic parameters, additionally, at 1, 2, and 10 °C min^?1 in the atmosphere containing 80% of Ar and 20% of O₂. The differential isoconversional method of Friedman was used to calculate the kinetic parameters. The results obtained indicate that thermooxidative decomposition of urea as well as the blends of urea with lime-containing materials and urea prills coated with limestone or dolomite powder follows a complex reaction mechanism.     

TG-FTIR/MS analysis of thermal and kinetic characteristics of some coal samples

Thermooxidative decomposition (TOD) of seven coal samples from different deposits (Bulgaria, Russia, Ukraine) was studied with the aim to determine characteristics of the process and the differences related to the origin of the coal samples studied. The experiments with a Setaram Setsys 1750 or Labsys Evo 1600 thermoanalyzers coupled to a Nicolet 380 FTIR spectrometer or Pfeiffer mass spectrometer, respectively, were carried out under non-isothermal heating conditions up to 1,000 °C at the heating rates of 1, 2, 5, 10, and 20 °C min^?1 in an oxidizing atmosphere. A model-free kinetic analysis approach based on the differential isoconversional method of Friedman was used to calculate the kinetic parameters. The combined TG-FTIR and TG-MS study of TOD of the coal samples made it possible to identify a number of gaseous species formed and evolved at that as well as to determine the differences in the thermal behavior of the coal samples and in the emission profiles of these species depending on their origin. The value of activation energy E along the reaction progress α varied more for the samples with higher content of organic matter and, especially, for the samples having at that also quite high content of mineral matter, indicating to the close association of mineral matter with organic matter and fixed carbon.