Q-switch of a continuously pumped CO2 laser with a scanning coupled-cavity Michelson mirror

We report on the possibility of Q-switching a continuously pumped CO₂ laser using a scanning Michelson interferometer as an end mirror, instead of the habitual well-known strategies. This method, in addition to its simplicity, produces free tail relaxation pulses having duration of about 1.3 μs, which is comparable to what can be obtained when using a saturable absorber. A pulse repetition frequency as high as 90 kHz is obtained.     

Analytic Representations Based on SU(1,1) Lie Algebra Coherent States for Squeezed Displaced Fock States

The coherent states (CSs) of the SU(1,1) group can be divided into two broad categories: (a) the Barut-Girardello coherent states (BGCSs) and (b) the Perelomov coherent states (PCSs). Some definitions for the squeezed displaced Fock states (SDFSs) are given. The hyperbolic analytic representation in the complex plane is considered. An analytic representation of the SU(1,1) Lie group is given and the representation in the unit disk based on the SU(1,1) PCSs for SDFSs is considered.      

Synthesis of several new lanthanide Glimepiride complexes for evaluation of microbial activity

The complexation between lanthanide metal ions like Nd(III), Tb(III), and Er(III) with Glimepiride produces 1: 1 molar ratio (metal: Glimepiride) monodentate complexes of general formula: [M(GMP)(H₂O)₄]Cl₃·xH₂O, where: M = Nd, Tb, and Er, x = 1, 10, respectively. The structures of obtained compounds were assigned by IR, ¹H NMR and UV/Vis spectra. Themogravimetric analysis and kinetic thermodynamic parameters have proved the thermal stability of Glimepiride complexes. Obtained lanthanide complexes showed significant effect against some bacteria and fungi.     

Palladium-Mediated Cyclization on Carbohydrate Templates. 3. Extension of The Cyclization to the Threo Series.

ABSTRACT

The palladium(0)-catalyzed Heck-type cyclization-β-alkoxy elimination reaction leading to enantiopure bicyclic compounds in the case of erythro 2,3-unsaturated glycosides has been successfully extended to the threo stereoisomer by only changing the aglycon moiety from an ethoxy group to an aryloxy moiety.     

Extraction of Effective Cement Paste Diffusivities from X-ray Microtomography Scans

The problem of extracting effective diffusivities of cement pastes on the basis of X-ray microtomography images is considered. A general computational homogenization framework is developed and applied to a variety of cement pastes whose microstructure has been digitized to a resolution of 1 μm. At this resolution, important submicron features are not resolved. Consequently, we propose a methodology whereby the pore space is ascribed a diffusivity less than the free diffusivity. For this purpose, a simple rule that incorporates microtomography data is proposed and shown to yield satisfactory results.     

Site-dependent activity of atomic Ti catalysts in Al-based hydrogen storage materials

Doping catalytically inactive materials with dispersed atoms of an active species is a promising route toward realizing ultradilute binary catalyst systems. Beyond catalysis, strategically placed metal atoms can accelerate a wide range of solid-state reactions, particularly in hydrogen storage processes. Here we analyze the role of atomic Ti catalysts in the hydrogenation of Al-based hydrogen storage materials. We show that Ti atoms near the Al surface activate gas-phase H(2), a key step toward hydrogenation. By controlling the placement of Ti, we have found that the overall reaction, comprising H(2) dissociation and H spillover onto the Al surface, is governed by a pronounced trade-off between lowering of the H(2) dissociation barrier and trapping of the products near the active site, with a sharp maximum in the overall activity for Ti in the subsurface layer. Our findings demonstrate the importance of controlling the placement of the active species in optimizing the activity of dilute binary systems.     

Aggregation behavior and intermicellar interactions of cationic Gemini surfactants: Effects of alkyl chain,spacer lengths and temperature

The aggregation behavior of the cationic Gemini surfactants C_mH_2m+1N(CH₃)₂(CH₂)_S (CH₃)₂ N C_mH_2m+1,2Br^? with m = 12, 14 and s = 2, 4 were studied by performing surface tension, electrical conductivity, pulsed field gradient nuclear magnetic resonance (PFG-NMR), and cyclic voltammetry (CV) measurements over the temperature range 298 K to 323 K. The critical micelle concentration (CMC), surface excess (Г_max), mean molecular surface area (A_min), degree of counter ion dissociation (α), and the thermodynamic parameters of micellization were determined from the surface tension and conductance data. An enthalpy–entropy compensation effect was observed and all the plots of enthalpy–entropy compensation exhibit excellent linearity. The micellar self-diffusion coefficients (D_m) and intermicellar interaction parameters (k_d) were obtained from the PFG-NMR and CV measurements. These results are discussed in terms of the intermicellar interactions, the effects of the chain and spacer lengths on the micellar surface charge density, and the phase transition between spherical and rod geometries. The intermicellar interaction parameters were found to decrease slightly with increasing temperature for 14–4–14, which suggests that the micellar surface charge density decreases with increasing temperature. The mean values of the hydrodynamic radius, R_h, and the aggregation number, N_agg, of the Gemini surfactants’ m–4–m micelles were calculated from the micellar self-diffusion coefficient. Moreover, the N_agg values were calculated theoretically. The experimental values of N_agg increase with increases in the chain length and are in good agreement with both previous results and our theoretical results.     

Effect of some nitrogen-heterocyclic compounds on corrosion of tin, indium, and their alloys in HClO4

Abstract  

The effect of adenine, adenosine, and 2,4,6-tris(2-pyridyl)-1,3,5-triazine (TPTZ) on the electrochemical and corrosion behavior of tin, indium, and tin-indium alloys in 0.5 M HClO₄ solution at different temperatures was studied. The inhibition efficiency increases with an increase in the concentration of adenine and adenosine in the case of tin and indium. However, the effect of two mentioned compounds on the corrosion rate of the studied alloys gives an opposite effect. In the presence of TPTZ, the inhibition efficiency increases as the concentration of the inhibitor is increased in the case of tin. In the case of both indium and its investigated alloys, the maximum inhibition efficiency is obtained at the lowest concentration of TPTZ (10⁻⁶ M). The adsorption of the studied compounds is found to obey the Frumkin adsorption isotherm. The standard enthalpy \Updelta H_ads^° , \Updelta H_{\rm ads}^{^\circ } , entropy \Updelta S_ads^° , \Updelta S_{\rm ads}^{^\circ } , and free energy changes of adsorption \Updelta G_ads^° \Updelta G_{\rm ads}^{^\circ } are calculated and discussed.