Effect of absorbed pump power on the quality of output beam from monolithic microchip lasers

The dependence of the beam propagation factor (M ² parameter) with the absorbed pump power in the case of monolithic microchip laser under face-cooled configuration is extensively studied. Our investigations show that the M ₂ parameter is related to the absorbed pump power through two parameters (α and β) whose values depend on the laser material properties and laser configuration. We have shown that one parameter arises due to the oscillation of higher order modes in the microchip cavity and the other parameter accounts for the spherical aberration associated with the thermal lens induced by the pump beam. Such dependency of M ² parameter with the absorbed pump power is experimentally verified for a face-cooled monolithic microchip laser based on Nd³⁺ -doped GdVO₄ crystal and the values of α and β parameters were estimated from the experimentally measured data points.     

Investigating laser rapid manufacturing for Inconel-625 components

This paper presents an investigation of laser rapid manufacturing (LRM) for Inconel-625 components. LRM is an upcoming rapid manufacturing technology, it is similar to laser cladding at process level with different end applications. In general, laser-cladding technique is used to deposit materials on the substrate either to improve the surface properties or to refurbish the worn out parts, while LRM is capable of near-net shaping the components by layer-by-layer deposition of the material directly from CAD model. In the present study, a high-power continuous wave (CW) CO₂ laser system, integrated with a co-axial powder-feeding system and a three-axis workstation were used. The effect of processing parameters during LRM of Inconel-625 was studied and the optimum set of parameters for the maximum deposition rate was established employing Orthogonal L9 array of Taguchi technique. Results indicated that the powder feed rate and the scan speed contributed about 56% and 26%, respectively to the deposition rate, while the influence of laser power was limited to 10% only. Fabricated components were subjected to non-destructive testing (like—ultrasonic testing, dye-penetrant testing), tensile testing, impact testing, metallographic examinations and micro-hardness measurement. The test results revealed defect-free material deposition with improved mechanical strength without sacrificing the ductility.     

Modification of magnetic anisotropy in metallic glasses using high-energy ion beam irradiation

Heavy ion irradiation in the electronic stopping power region induces macroscopic dimensional change in metallic glasses and introduces magnetic anisotropy in some magnetic materials. The present work is on the irradiation study of ferromagnetic metallic glasses, where both dimensional change and modification of magnetic anisotropy are expected. Magnetic anisotropy was measured using Mössbauer spectroscopy of virgin and irradiated Fe₄₀Ni₄₀B₂₀ and Fe₄₀Ni₃₈Mo₄B₁₈ metallic glass ribbons. 90 MeV ¹²⁷I beam was used for the irradiations. Irradiation doses were 5×10¹³ and 7.5×10¹³ ions/cm². The relative intensity ratios D ₂₃ of the second and third lines of the Mössbauer spectra were measured to determine the magnetic anisotropy. The virgin samples of both the materials display in-plane magnetic anisotropy, i.e., the spins are oriented parallel to the ribbon plane. Irradiation is found to cause reduction in magnetic anisotropy. Near-complete randomization of magnetic moments is observed at high irradiation doses. Correlation is found between the residual stresses introduced by ion irradiation and the change in magnetic anisotropy.     

Thermal analysis of lanthanide polyphosphates

Summary A study of thermal analysis of some lanthanide polyphosphates has been reported. The DTA curves of Ce, Pr and Sm polyphosphates were of similar nature. They exhibited a sharp exothermic peak indicating crystallization temperature (T _c) around 520 °C. However, no peak indicatingT _m was observed upto 800 °C. TG curves of Ce, La, Pr, Sm, Y polyphosphates indicated weight loss occurring in three stages. The integral procedural decomposition thermal analysis (ipdt) indicated that these materials had refractory nature.With 4 figures and 2 tables     

Floating spherical Gaussian orbital model study of average electric polarisabilities and magnetic susceptibilities: Some aliphatic hydrocarbons

Floating spherical Gaussian orbital model is used to discuss the average electric polarisabilities and magnetic susceptibilities of a series of hydrocarbons. It has been noticed that the core contributions are negligibly small and these quantities (average electric polarisabilities and magnetic susceptibilities) can be well estimated from contributions localised on bond Gaussians.     

1-Phenyl-6,7-disubstituted-aminopropyl)-1,2,3,4-tetrahydroisoquinolines as possible antituberculer agents

The Condensation of 3,4-disubstituted phenylethylamine and benzaldehyde furnished l-phenyl-6,7-disubstituted-1,2,3,4-tetrahydroisoquinolines l. which on reaction with 1,3-dibromopropane gave l-phenyl-6,7-disubstituted-2-(3-bromoprophyl)-1,2,3,4-tetrahydroisoquinolines 2. The reaction of 2 with different secondary amines resulted in the synthesis of 3. The compounds 3 were screened for their in vitro antituberculer activity against Mycobacterium smegmatis, and some of them have been found to be total inhibitors of M. Smegmatis     

Rapid determination of molybdenum in ferromolybdenum and molybdenum additives, with oxine

A rapid method is presented for the gravimetric determination of molybdenum (as the oxinate) in ferromolybdenum and molybdenum additives. The sample is fused with a mixed flux of sodium peroxide and sodium carbonate in a zirconium crucible for complete decomposition. Leaching the cooled fusion cake with water provides instantaneous separation of molybdenum as sodium molybdate from iron(III) and other hydrous oxides. After filtration, the molybdenum is precipitated with oxine after addition of EDTA and oxalate to obviate interference from other metal oxinates, and determined gravimetrically. The precision and accuracy are comparable to those of referee methods.     

Self-assembled,wormlike-cylinder network of polystyrene-block-poly(ethylene oxide) micelles in solution

We report the formation of a highly entangled and interconnected, self-assembled, wormlike-cylinder network of polystyrene-block-poly(ethylene oxide) in N, N-dimethylformamide/water. In this system, N,N-dimethylformamide was a common solvent and water was a selective solvent for the poly(ethylene oxide) blocks. The degrees of polymerization of the polystyrene and poly(ethylene oxide) blocks were 962 and 227, respectively. The network was formed at copolymer concentrations higher than 0.4 wt % and consisted of self-assembled, wormlike cylinders that were interconnected by Y-shaped, T-shaped, and multiple junctions. The network morphology was visualized with transmission electron microscopy. Capillary viscometry measurements revealed an order-of-magnitude increase in the inherent viscosity of the colloidal system upon the formation of the network. A similar effort to obtain a wormlike-cylinder network in an N,N-dimethylformamide/acetonitrile system, in which acetonitrile was a selective solvent for the poly(ethylene oxide) blocks, was unsuccessful even at high copolymer concentrations; instead, the wormlike cylinders showed a tendency to align. The viscosity measurements also did not show a substantial increase in the inherent viscosity. Thus, the solvent played a critical role in determining the formation of the self-assembled, wormlike-cylinder network. This formation of the network resulted from an interplay between the end-capping energy, bending energy (curvature), and configurational entropy of the self-assembled, wormlike-cylinder micelles that minimized the free energy. © 2006 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 44: 3605–3611, 2006     

Rapid spectrophotonietric determination of copper in steel with zinc dibenzyldithiocarbamate

A rapid spectrophotometric method employing zinc dibenzyldithiocarbamate is described for determining copper in a wide variety of steels. The acidity is not critical (0.5-2N) and the colour of the complex is stable for > 1 hr. The range of the method is 0.005-5% copper and 6 samples can be analysed in about an hour.