Separation of isomeric and nonisomeric monoribonucleotides by isocratic ion pair high performance liquid chromatography

A simple, isocratic, high performance liquid chromatographic procedure is described for the first time for the separation of nine monoribonucleotides using the ion-pairing technique. An aqueous mobile phase containing 100 mM KH₂PO₄ and 12.5 mM tetramethylammonium hydroxide as the solvophobic ion, pH 3.9, was used with a reverse phase RP-18 column. The nine monoribonucleotides studied were separated and eluted in the following order: cytidine-5′ -phosphate, uridine-5′ -phosphate, cytidine-3′ -phosphate, guanosine-5′ -phosphate, uridine-3′ -phosphate, uridine-2′ -phosphate, adenosine-5′ -phosphate, guanosine-3′ -phosphate, and adenosine-3′ -phosphate. Generally the 5′ nucleotides eluted faster than the 3′ and the order of elution within each series was: cytidine, uridine, guanosine, and adenosine. The only nucleotide where three isomers were studied was uridine, and the 2′ eluted later than the 3′. Baseline separation was attained for a mixture containing four 3′ nucleotides and uridine-2′ -phosphate. When the four 5′ nucleotides were chromatographed, baseline separation was also obtained except between cytidine-5′ -phosphate and uridine-5′ -phosphate. The coefficient of variation of the retention characteristics, which reflected day-to-day variation, averaged 6.4%.     

Selective lateral metalation and electrophilic quenching of c-4 functionalized isoxazoles. IX. Direct formation of the C-N bond utilizing an electrophilic nitrogen source

C-5 Lithio-alkylisoxazoles were quenched with dialkyl azodicarboxylates to form the C-5 alkylhydrazine derivatives in synthetically useful yields.     

Experimental Study of Pore-Scale Mechanisms of Carbonated Water Injection

Carbon dioxide (CO₂) injection is a well-established method for increasing recovery from oil reservoirs. However, poor sweep efficiency has been reported in many CO₂ injection projects due to the high mobility contrast between CO₂ and oil and water. Various injection strategies including gravity stable, WAG and SWAG have been suggested and, to some extent, applied in the field to alleviate this problem. An alternative injection strategy is carbonated water injection (CWI). In CWI, CO₂ is delivered to a much larger part of the reservoir compared to direct CO₂ injection due to a much improved sweep efficiency. In CWI, CO₂ is used efficiently and much less CO₂ is required compared to conventional CO₂ flooding, and hence the process is particularly attractive for reservoirs with limited access to large quantities of CO₂ (offshore reservoirs or reservoirs far away from inexpensive natural CO₂ resources). This article describes the results of a pore-scale study of the process of CWI by performing high-pressure visualisation flow experiments. The experimental results show that CWI, compared to unadulterated (conventional) water injection, improves oil recovery as both a secondary (before water flooding) and a tertiary (after water flooding) recovery method. The mechanisms of oil recovery by CWI include oil swelling, coalescence of the isolated oil ganglia and flow diversion due to flow restriction in some of the pores as a result of oil swelling and the resultant fluid redistribution. In this article the potential benefit of a subsequent depressurisation period on oil recovery after the CWI period is also investigated.     

Numerical Study of Ignition Process in Turbulent Shear-less Methane-air Mixing Layer

In this work, ignition process in a turbulent shear-less methane-air mixing layer is numerically investigated. A compressible large eddy simulation method with Smagorinsky sub-grid scale model is used to solve the flow field. Also, a thickened flame combustion model and DRM-19 reduced mechanism are used to compute species distribution and the heat release. Non-reacting mean and RMS axial velocity profiles and mean mixture fraction are validated against experimental data. Instantaneous mixture fraction contours show that the large bursts penetrate from the fuel stream into that of the oxidizer and vice versa and a random behaviour in the cross-stream direction. Flame kernel initiation, growth and propagation are analysed and compared with the experimental data. The ignition results show that the flame is not stable and blow-off occurs, but a more detailed investigation shows that local and short time flame stabilization exist during blow-off. During these local stabilization, heat release increased at the upstream edge of the flame. Most_upstream flame edge scalar analysis shows that the methane mass fraction has a dominant role in the local flame stabilization. OH, HO₂, CH₂O and heat release contours demonstration reveal that HO₂ and CH₂O mass fraction as well as the heat release reach a maximum on the border of the flame, but the maximum OH concentration is located in the middle of flame kernel.     

Transient thermal stresses in two-dimensional functionally graded thick hollow cylinder with finite length

In this paper transient thermal stresses in a thick hollow cylinder with finite length made of two-dimensional functionally graded material (2D-FGM) based on classical theory of thermoelasticity are considered. The volume fraction distribution of materials, geometry and thermal load are assumed to be axisymmetric but not uniform along the axial direction. The finite element method with graded material properties within each element is used to model the structure. Temperature, displacements and stress distributions through the cylinder at different times are investigated. Also the effects of variation of material distribution in two radial and axial directions on the thermal stress distribution and time responses are studied. The achieved results show that using 2D-FGM leads to a more flexible design so that time responses of structure, maximum amplitude of stresses and uniformity of stress distributions can be modified to a required manner by selecting suitable material distribution profiles in two directions.     

Kinetic determination of thiocyanate on the basis of its catalytic effect on the oxidation of methylene blue with potassium bromate.

This study reports a sensitive kinetic spectrophotometric method for the determination of trace amounts of thiocyanate. In acidic solution, Methylene Blue (MB) is oxidized by bromate to form a colorless compound. The reaction is accelerated by trace amounts of thiocyanate and can be followed by measuring the absorbance at 664 nm. The absorbance of the reaction decreased with an increase in the reaction time. Under the optimum experimental conditions (0.56 M of sulfuric acid, 3.9 x 10(-5) M of MB, 3.0 x 10(-3) M of bromate, 180 s, 25 degrees C), thiocyanate can be determined in the range 5.0 - 180 ng/ml. The relative standard deviations (n = 8) are 2.81 and 1.43% for 10.0 and 150 ng/ml thiocyanate, respectively. The detection limit of this method is (3sigma) 3.8 ng/ml. This method was successfully applied to the determination of thiocyanate in real samples.     

Study of interface mixing induced by Ar<Superscript>+</Superscript> ion irradiation on Ag–Ge bilayer system

A 400 keV ⁴⁰Ar⁺ ion beam was utilized to induce mixing between two thin layers of Ag and Ge. Rutherford Backscattering Spectrometry and Electrical Resistivity Measurements were employed as probes to investigate the kinetics of ion mixing. The intermixed region was studied at several fluences up to 1.7×10¹⁷ ions/cm² at a constant flux of 0.25 μA/cm². The “RUMP” simulation computer code was used to assist in the evaluation of the experimental results from the spectra. The analysis of the Rutherford Backscattering Spectrometry spectra shows that increasing the Ar⁺ fluence enhances the Ag–Ge intermixing. To describe the mixing process, mixing rate parameters were calculated and compared with the theoretical models’ predictions. Børgesen’s local thermal spike model was found to accurately predict the diffusion in the Ag–Ge interface. An increase in the electrical resistivity of the film was detected during irradiation.     

Theoretical studies on tautomerism of tetrazole derivatives by polarisable continuum method (PCM)

Computational calculations at B3LYP/6-31++G(d,p) level were employed in the study of the predominant tautomeric forms of 1-H and 2-H tetrazole derivatives (5-NO₂, 5-CF₃, 5-F, 5-H, 5-NH₂, 5-OH, 5-CH₃) in the gas phase and solution using PCM model. For electron withdrawing derivatives in the gas phase and solution 2-H forms are more stable and dominant form. For electron releasing groups in the gas phase and solution with low dielectric constants the 2-H form is more stable but in solvents with high dielectric constants 1-H isomer is dominant form. In addition variation of dipole moments and charges on atoms in the solvents are studied.