Thermodynamical evaluation of usefulness of future hydrocarbon fuels for use in compression ignition engines

The paper discusses the issues of the influence of the fuel spray formation on the generation of self-ignition spots and the development of pre-flame processes in the cylinder of a model diesel engine. The investigations were carried out for a standard diesel fuel and two other types of fuel that were mixtures of ethanol, butanol, and diethylether in a variety of proportions. By applying optical methods of analysis, the authors determined the geometrical indexes of the injected fuel spray as well as fuel mass distribution in the longitudinal and transverse cross section of the fuel spray during the injection process. The location and number of the self-ignition spots in the combustion chamber were evaluated on the basis of a comparison under various conditions: in presence of the charge swirl and at the lack of it. Research conducted for the single-cylinder engine confirmed the possibility of the use of diesel-like fuels for compression ignition engines.

     

In Metric-measure Spaces Sobolev Embedding is Equivalent to a Lower Bound for the Measure

We study Sobolev inequalities on doubling metric measure spaces. We investigate the relation between Sobolev embeddings and lower bound for measure. In particular, we prove that if the Sobolev inequality holds, then the measure μ satisfies the lower bound, i.e. there exists b such that μ(B(x,r))≥b r ^α for r∈(0,1] and any point x from metric space.     

The Development and Validation of a Stability-Indicating UHPLC-DAD Method for Determination of Perindopril l-Arginine in Bulk Substance and Pharmaceutical Dosage Form

A stability-indicating ultra-high-performance liquid chromatography (UHPLC) method with a diode array detector was developed and validated for the determination of cis/trans isomers of perindopril l-arginine in bulk substance and pharmaceutical dosage form. The separation was achieved on a Poroshell 120 Hilic (4.6 × 150 mm, 2.7 µm) column using a mobile phase composed of acetonitrile–0.1 % formic acid (20:80 v/v) at a flow rate of 1 mL min^?1. The injection volume was 5.0 µL and the wavelength of detection was controlled at 230 nm. The selectivity of the UHPLC-DAD method was confirmed by determining perindopril l-arginine in the presence of degradation products formed during acid–base hydrolysis and oxidation as well as degradation in the solid state, at an increased relative air humidity and in dry air. The method’s linearity was investigated in the ranges 0.40–1.40 µg mL^?1 for isomer I and 0.40–2.40 µg mL^?1 for isomer II of perindopril l-arginine. The UHPLC-DAD method met the precision and accuracy criteria for the determination of the isomers of perindopril l-arginine. The limits of detection and quantitation were 0.1503 and 0.4555 µg mL^?1 for isomer I and 0.0356 and 0.1078 µg mL^?1 for isomer II, respectively.     

Nearest interval approximation of a fuzzy number

The problem of the interval approximation of fuzzy numbers is discussed. A new interval approximation operator, which is the best one with respect to a certain measure of distance between fuzzy numbers, is suggested.     

A New Route to Light Emitting Organic Materials Based on Triazine Derivatives

Novel light-emitting organic materials comprising conjugated oligomers chemically attached via a flexible spacer to an electron–or hole-conducting core were synthesized by Stille cross-coupling methodology and designed for tunable charge injection and optical properties. The hyperbranched structures have been characterized by ¹H NMR, ¹³C NMR, and UV-VIS spectroscopy. The obtained structures show good stability in common organic solvents such as CHCl₃, toluene, and CH₂Cl₂ and exhibit excellent thermal stability. A preliminary electroluminescence properties were also investigated. This class of materials will help to balance charge injection and transport and to spread out the charge recombination zone, thereby significantly improving the device efficiency and lifetime of unpolarized and polarized OLEDs.     

Mechanism of the Verwey transition in magnetite

By combining ab initio results for the electronic structure and phonon spectrum with the group theory, we establish the origin of the Verwey transition in Fe3O4. Two primary order parameters with X3 and Delta5 symmetries are identified. They induce the phase transformation from the high-temperature cubic to the low-temperature monoclinic structure. The on-site Coulomb interaction U between 3d electrons at Fe ions plays a crucial role in this transition--it amplifies the coupling of phonons to conduction electrons and thus opens a gap at the Fermi energy.     

Comment on “Entanglement of two interacting bosons in a two-dimensional isotropic harmonic trap” [Phys. Lett. A 373 (2009) 3833]

The correct form of the Schmidt decomposition of the stationary wave functions for a system of two interacting particles trapped in a two-dimensional harmonic potential is given.     

Preliminary thermal characterization of natural resins from different botanical sources and geological environments

The preliminary studies on thermal behavior of differently aged natural resins from Russia (Khatanga), Dominican Republic (El Valle), Colombia and Poland (Jantar) were performed. Thermal stability and behavior under elevated temperature were investigated by thermogravimetry (TG) and differential scanning calorimetry (DSC), while the differences in the structure and composition by FT-IR spectroscopy. Analyzed resins show different thermal effects during heating suggesting that possible post-reactions and structural changes occurred. TG results indicated that Dominican, Russian and Colombian resins present relatively high thermal stability under air conditions in the range of 228–300 °C, whereas the mass loss of 5mass% at about 217 °C was observed for Baltic amber. During DSC experiments, the analyzed resins expose thermal events which make impossible determination of glass transition temperature in a raw sample. The results indicate that both TG and DSC cannot be considered as methods for age dating of natural resins and more advanced techniques should be applied. Careful analysis of FT-IR data in the carbonyl region may provide additional information about the composition and history of the natural resin.

     

LIF excitation spectra for S0 → S1 transition of anthranilic acid: Detailed studies

Laser-induced fluorescence (LIF) excitation spectra of jet-cooled molecules of anthranilic acid were investigated. In order to distinguish bands belonging to the monomer from those belonging to the dimer species three different spectra were recorded under conditions which differed in the value of partial pressure of vapours of anthranilic acid. Narrow bandwidth of rotational profiles in the acquired spectra made it possible to resolve new interesting spectral features and to analyse the rather small anharmonicity in progressions of several low-frequency vibrations. Eleven fundamental bands up to ca. 1400 cm⁻¹ and five overtones of out-of-plane vibrations were assigned. Simulation based on approximate relations of the experimental band intensities of overtones and combination bands with respect to fundamental bands was carried out. This simulation was found a simple and practical tool in analysis of the spectra and an aid to verify the proposed assignment.Harmonic and anharmonic frequencies of vibrational modes were calculated using the HF/6-31G∗∗ and CIS/6-31G∗∗ methods for the S₀ and S₁ state, respectively. Modelling of band intensities using displacement parameters derived from the results of the ab initio calculations was performed. This modelling significantly underestimates the displacement parameters. The Dushinsky matrix derived from the results of the ab initio calculations was used to check the validity of the models and to find modes which undergo large frequency changes and mode mixing upon electronic excitation.