Unsteady flow of viscoelastic fluid between two cylinders using fractional Maxwell model

The unsteady flow of an incompressible fractional Maxwell fluid between two infinite coaxial cylinders is studied by means of integral transforms.The motion of the fluid is due to the inner cylinder that applies a time dependent torsional shear to the fluid.The exact solutions for velocity and shear stress are presented in series form in terms of some generalized functions.They can easily be particularized to give similar solutions for Maxwell and Newtonian fluids.Finally,the influence of pertinent parameters on the fluid motion,as well as a comparison between models,is highlighted by graphical illustrations.     

The Rayleigh–Stokes problem for an edge in a generalized Oldroyd-B fluid

The velocity field corresponding to the Rayleigh–Stokes problem for an edge, in an incompressible generalized Oldroyd-B fluid has been established by means of the double Fourier sine and Laplace transforms. The fractional calculus approach is used in the constitutive relationship of the fluid model. The obtained solution, written in terms of the generalized G-functions, is presented as a sum of the Newtonian solution and the corresponding non-Newtonian contribution. The solution for generalized Maxwell fluids, as well as those for ordinary Maxwell and Oldroyd-B fluids, performing the same motion, is obtained as a limiting case of the present solution. This solution can be also specialized to give the similar solution for generalized second grade fluids. However, for simplicity, a new and simpler exact solution is established for these fluids. For β → 1, this last solution reduces to a previous solution obtained by a different technique.      

Decay of a potential vortex and propagation of a heat wave in a second grade fluid

The propagation of a heat wave in an incompressible second grade fluid within the context of a potential vortex is studied. The solutions for the Newtonian fluid can be obtained from those for fluids of second grade as a limiting case.     

Li17Ag3Sn6: a polar intermetallic pi-system with carbonate-like [AgSn3]11- anions and trefoil aromatic [Ag2Sn3]6- layers

A new lithium silver stannide, Li17Ag3Sn6, was synthesized from high-temperature reactions of the pure elements in tantalum containers. Its crystal structure, in the space group, P31m, with a = 8.063(3) A, c = 8.509(4) A, Z = 1, features two distinct AgSn-based anionic layers. Defect graphitic layers of Ag2Sn3, with ordered vacancies at one-third of the Ag sites, are alternately stacked with Kagome-like nets of isolated trigonal planar AgSn3 units. Double layers of Li ions are sandwiched between the stacked AgSn-based layers. Theoretical calculations show unusual pi-interactions within both anionic layers, with the trigonal planar [AgSn3]11- units being isoelectronic with CO(3)2-. In addition, the chemical bonding of the layered [Ag2Sn3]6- pi-network features incompletely filled lone-pair Sn states involved in in-plane trefoil aromatic interactions. Transport and magnetic susceptibility measurements on Li17Ag3Sn6 indicate excellent metallic behavior and temperature-independent paramagnetism consistent with results from band structure calculations. The "trefoil" aromaticity, previously postulated for aromatic molecular systems, is finally observed, albeit in a polar intermetallic solid-state structure that lies at the border between metals and nonmetals.     

Quality and Human Health Risk Assessment of Metals and Nitrogen Compounds in Drinking Water from an Urban Area Near a Former Non-Ferrous Ore Smelter

The quality and potential health risk of drinking waters in Medias, a town near a former non-ferrous ore smelter in Romania, was assessed using the drinking water quality index (DWQI), hazard quotient (HQ) and total hazard quotient (THQ). A total of 29 water samples collected from 26 wells and 3 springs used as drinking water sources, located in near proximity to agricultural, industrial or household contamination sources, were characterized. The obtained results indicated high NO₂^?, NO₃^?, Cd and Mn levels that exceeded the corresponding maximum allowable concentrations. According to the DWQI values, only 10% of water sources have acceptable quality, while 21% are threatened, and 69% have poor- quality. The health risk assessment suggested a high risk for NO₃^? for more than 72% of the drinking waters HQ_NO3^??>?1.0 but no risk for metals and NO₂^? (HQ_metals< 1.0; HQ_NO2^?< 1.0).     

Accurate Determination of Trace Amounts of Oxygen in CrAlN Hard Coatings by a Combination of WDS–EPMA and SIMS

Low amounts of oxygen in AlCrN hard coatings have been quantitatively analysed by means of WDS–EPMA. By combination with SIMS depth profiling, applying a calibration sample produced by ion implantation, the accuracy of the EPMA results was proven. Values as low as 0.07 at% were measured and the calculated detection limit is in the range of 0.01 at%.     

Chemistry of cobalt acetate. 7. Electrochemical oxidation of mu3-oxo-centered cobalt(III) acetate trimers

Electrochemical and spectroelectrochemical properties of five cobalt(III) acetate complexes [CoIII3(mu3-O)(CH3CO2)5(OR)(py)3][PF6] are described, where py=pyridine and R=OCCH3 (A), H (B), CH3 (C), CH2CH=CH2 (D), and CH2C6H5 (E). Each is reduced irreversibly as observed by cyclic voltammetry at room temperature and at -40 degrees C in acetonitrile at scan rates up to 20 V s(-1), but oxidized reversibly to a mixed-valence Co(III)2Co(IV) species at approximately 1.23 V vs the ferrocenium/ferrocene couple. Controlled potential coulometry confirmed a one-electron-oxidation process. Spectroelectrochemical oxidation of A at 5 degrees C showed isosbestic points in the electronic absorption spectrum that showed the oxidized complex to be stable in solution for at least 1 h.     

X-ray and neutron diffraction studies on "Li4.4Sn"

A chemical analysis and detailed structural characterization, using X-ray single crystal and neutron powder diffraction, of the binary lithium-tin compound "Li(4.4)Sn" is presented. Phase analyses and subsequent structural refinements result in the reformulation of "Li(4.4)Sn" as Li(17)Sn(4). The lithium-rich binary phase crystallizes with a complex cubic structure in the space group Ffourmacr;3m, with a = 19.6907(11) A, Z = 20. The improved crystal structure determination indicates well-defined lithium atom positions, some of which differ from those previously reported. The nearly Zintl phase Li(17)Sn(4) exhibits poor metallic behavior similar to that of heavily doped semiconductors. Comparisons of the refined crystal structure with previously reported X-ray crystal structures associated with "Li(4.4)Sn" are discussed.     

On the copolymerization model and microstructure of methyl acrylate - styrene radical copolymer. Influence of ZnCl2

Bulk radical copolymerization of methyl acrylate (MeA, M₁) with styrene (St, M₂) in presence and absence of ZnCl₂ as complexing agent was studied. ¹H-NMR spectra were used to establish copolymer composition and sequence distribution. The methoxy group signal was observed to be split due to pentads, but the analysis of sequence distribution is possible only at triad level. Both composition and sequence distribution data confirmed that bulk radical copolymerization respects quite well the terminal addition model; the values of r₁ = 0.14 ± 0.02 (from composition data) and r₁ = 0.25 ± 0.03 (from sequence distribution data) and r₂ = 0.83 ± 0.10 (from composition data) were found. The presence of ZnCl₂ increases the probability of alternating addition, e.g., for [ZnCl₂]/[MeA] = 0.2, r₁ = 0.03 ± 0.02 and r₂ = 0.17 ± 0.03. The radical copolymer obtained in bulk in the absence of ZnCl₂ presents a coisotactic configuration with σ = 0.75 ± 0.03, but the presence of the complexing agent reduces the probability of coisotactic addition, e.g., for [ZnCl₂]/[MeA] = 0.2, σ = 0.52 ± 0.03.     

Exact solutions for the flow of an Oldroyd-B fluid due to an infinite flat plate

The unsteady flow of an Oldroyd-B fluid due to an infinite flat plate, subject to a translation motion of linear time-dependent velocity in its plane, is studied by means of the Laplace transform. The velocity field and the associated tangential stress corresponding to the flow induced by the constantly accelerating plate as well as those produced by the impulsive motion of the plate are obtained as special cases. The solutions that have been determined, in all accordance with the solutions established using the Fourier transform, reduce to those for a Newtonian fluid as a limiting case. The similar solutions for a Maxwell fluid are also obtained.