Observation of curious spiral growth features in Tl doped Hg bearing high temperature superconducting tapes

Synthesis of Hg(Tl)Ba ₂ Ca ₂ Cu ₃ O _8+δ superconducting tapes have been accomplished by annealing the precursor tape, Ba ₂ Ca ₂ Cu ₃ O _y (fabricated by doctor blade tape casting technique) in an environment of Hg(Tl) vapour. Characterization of superconducting HTSC tape sample was carried out through XRD, TEM, SEM and R-T measurements. Surface morphological investigations of the as-synthesized Hg(Tl)Ba ₂ Ca ₂ Cu ₃ O _8+δ HTSC tapes by scanning electron microscope have shown the occurrence of curious growth characteristics resembling spiral like features. These growth spirals encompass nearly the whole grain suggesting that spiral growth led to the formation of small crystal like grains of superconducting material Hg(Tl)Ba ₂ Ca ₂ Cu ₂ O _8+δ .The likely mechanism for the generation of these screw dislocations has been elucidated in terms of incoherent coalescence of growth fronts formed from Hg(Tl):1223 and Hg(Tl):1234 nuclei.     

Synthesis and luminescence properties of Eu2+-activated Ca4Mg5(PO4)6 for blue-emitting phosphor

Ca ₄ Mg ₅ (PO ₄ ) ₆ :Eu²⁺^{\boldsymbol{2+}} blue-emitting phosphor was synthesized by the combustion-assisted synthesis method under reductive atmosphere. The products were characterized by powder X-ray diffraction (XRD), transmission electron microscopy (TEM) and photoluminescence (PL) spectrum. XRD analysis confirmed the formation of Ca ₄ Mg ₅ (PO ₄ ) ₆ pure phase. Photoluminescence results showed that the phosphor can be excited efficiently by UV light range from 230–400 nm, and then exhibited bright blue light with peak wavelength at 431 nm. It is a very promising candidate as a blue-emitting phosphor for potential applications in display devices.     

Preparation of Sm-Ru bimetallic alloy films on Ru(0001) surface by vapour-deposition and annealing

Sm-Ru intermetallic surface alloy films were prepared by vacuum deposition and annealing of rare earth Sm on single crystal Ru(0001) surface. The Ru 3 d and Sm 3 d core level spectra clearly show the formation of surface alloy layers. XPS measurements on surface alloy film revealed an induced peak in the Ru 3 d region at lower binding energy by 1 eV compared to the bulk Ru (elemental) suggesting an electronic effect of alloying and Sm-Ru bond formation. The Sm 3 d _5/2 photoemission peak of Sm film consists of strong features characteristic of Sm(II) with electron configuration 4 f ⁶ (5 d 6 s ) ² and Sm(III) with electron configuration 4 f ⁵ (5 d 6 s ) ³ .It is observed that the Sm(II) feature decreases in intensity upon alloy formation with surface Ru atoms. Oxidation of these films with carbon monoxide indicates alloy breakdown due to the oxidation of Sm atoms selectively. Alloy oxidation also shows a clear shift of Sm 3 d _5/2 feature.     

A new combustion route to γ-Fe2O3 synthesis

A new combustion route for the synthesis of γ-Fe ₂ O ₃ is reported by employing purified a-Fe ₂ O ₃ as a precursor in the present investigation. This synthesis which is similar to a self propagation combustion reaction, involves fewer steps, a shorter overall processing time, is a low energy reaction without the need of any explosives, and also the reaction is completed in a single step yielding magnetic iron oxide i.e. γ-Fe ₂ O ₃ .The as synthesized γ-Fe ₂ O ₃ is characterized employing thermal, XRD, SEM, magnetic hysteresis, and density measurements. The effect of ball-milling on magnetic properties is also presented.     

Homogenization of zinc distribution in vertical Bridgman grown Cd0.96Zn0.04Te crystals

One of the most pressing issues in the growth of high quality single crystal Cd _0.96 Zn _0.04 Te material, is to achieve homogenization of the high axial variation of Zn concentration, caused by the larger than unity segregation coefficient of Zn in CdTe. This is achieved in our crystals (i) by thermal annealing of the CdZnTe crystal, which redistributes the as grown Zn distribution by solid state diffusion of Zn (this solid state diffusion of Zn occurs at three stages (a) during the growth when the solidified crystal is near to the melting point temperature, (b) during the post growth annealing of the crystal at a high temperature and (c) during the cooldown to room temperature) and (ii) by the reduction of Zn segregation during the growth stage by enhanced convective mixing of the melt, through a proper choice of ampoule and furnace dimensions. By adopting suitable growth parameters and sufficient post growth annealing it has been possible to grow Cd _0.96 Zn _0.04 Te crystals, which have nearly 75% of their fraction within 1% Zn concentration variation.     

Fine structure at the diffusion welded interface of Fe3Al/Q235 dissimilar materials

The interface of Fe ₃ Al/Q235 dissimilar materials joint, which was made by vacuum diffusion welding, combines excellently. There are Fe ₃ Al, FeAl phases and α-Fe (Al) solid solution at the interface of Fe ₃ Al/Q235. Aluminum content decreases from 28% to 1.5% and corresponding phase changes from Fe ₃ Al with DO ₃ type body centred cubic bcc structure to α-Fe (Al) solid solution with B2 type bcc structure. All phases are present in sub-grain structure level and there is no obvious brittle phases or micro-defects such as pores and cracks at the interface of Fe ₃ Al/Q235 diffusion joint.     

Effect of zirconium addition on the recrystallization behaviour of a commercial Al-Cu-Mg alloy

It is well known that the second phase particles have an effect on recrystallization and grain growth behaviour of an alloy. Particularly the bimodal distribution of second phase particles has an effect which is opposite in sense where coarse second phase particles (> 1 μm) stimulate nucleation while fine particles exhibit Zener drag. In the literature, the effect of zirconium addition to aluminium alloys has been well documented in order to produce superplasticity by giving ultra fine grain size to the alloy. Addition of zirconium produces Al ₃ Zr particles which pin the grain boundaries during recrystallization and grain growth. In the present work, zirconium was added to a commercial Al-Cu-Mg alloy and by heat treatment Al ₃ Zr particles were precipitated and after forging, the grain size was an order of magnitude lower than the alloy without zirconium. Transmission electron microscopy was employed to characterize the second phase particles, i.e. Al ₃ Zr particles and found to be rod shaped and identified to be cubic ordered L 1 ₂ phase with a lattice parameter of 0.408 nm. Further, it was observed that fine (100 nm) Al ₃ Zr particles promote only continuous recrystallization which is polygonization of subgrains and subgrain growth. It was found that the fine dispersion of Al ₃ Zr particles inhibits both recrystallization and grain growth in the commercial Al-Cu-Mg alloy.     

Structural and electrical properties of Ta<Subscript><Emphasis Type="Bold">2</Emphasis></Subscript>O<Subscript><Emphasis Type="Bold">5</Emphasis></Subscript> thin films prepared by photo-induced CVD

Tantalum oxide (Ta ₂ O ₅ ) films and Al/Ta ₂ O ₅ /Si MOS capacitors were prepared at various powers by ultraviolet photo-inducing hot filament chemical vapour deposition (HFCVD). Effects of ultraviolet light powers on the structure and electrical properties of Ta ₂ O ₅ thin films were studied using X-ray diffraction (XRD) and atomic force microscopy (AFM). The dielectric constant, leakage current density and breakdown electric field of the samples were studied by the capacitance–voltage (C–V) and current–voltage (I–V) measurements of the Al/Ta ₂ O ₅ /Si MOS capacitors. Results show that the Ta ₂ O ₅ thin films grown without inducement of UV light belong to amorphous phase, whereas the samples grown with inducement of UV-light belong to δ-Ta ₂ O ₅ phase. The dielectric constant and leakage current density of the Ta ₂ O ₅ thin films increase with increasing powers of the UV- lamps. Effects of UV- lamp powers on the structural and electrical properties were discussed.     

Aqueous slip casting of MgAl2O4 spinel powder

A stoichiometric MgAl ₂ O ₄ spinel (MAS) powder was synthesized by calcining a compacted mixture of a\boldsymbol{\alpha} -Al ₂ O ₃ and calcined caustic MgO at 1400°C for 1 h and was surface treated against hydrolysis using an ethanol solution of H ₃ PO ₄ and Al(H ₂ PO ₄ ) ₃ after fine grinding. Aqueous suspensions with 41–45 vol.% treated powder were prepared using tetra methyl ammonium hydroxide (TMAH) and an ammonium salt of polyacrylic acid (Duramax D-3005) as dispersing agents. These stable suspensions were consolidated in plaster moulds by slip casting (SC) route for the first time. For comparison purposes, the treated powder was also compacted by die-pressing technique after converting into freeze-dried granules and sintered along with slip cast samples at 1550–1650°C for 1–2 h. The MAS ceramics fabricated by slip casting and die-pressing exhibited comparable properties.     

Synthesis and characterization of chiral liquid crystal polymers containing donor–acceptor group

A series of new chiral side-chain liquid crystalline polymers with electron donor–acceptor action were prepared containing chiral monomer with donor group and nematic LC monomer with acceptor group. All polymers were synthesized by graft polymerization using polymethylhydrosiloxane as backbone. The mesomorphic properties were investigated by differential scanning calorimetry (DSC), polarizing optical microscopy (POM), thermogravimetric analyses (TGA), and X-ray diffraction measurements (XRD). The chemical structures of monomers and polymers were confirmed by Fourier transform infrared (FTIR), proton nuclear magnetic resonance spectra (¹H NMR and ¹³CNMR). M ₁ did not show liquid crystalline phase and M ₂ turned out nematic phase on heating and cooling cycle. Polymers P ₂ –P ₇ were cholesteric phase. Cholesteric phase and low glass temperature liquid crystalline polymers have been obtained, which offered the possibility of application. Experimental results demonstrated that the glass-transition temperatures rose and isotropization temperatures decreased and the ranges of the mesophase temperature reduced with increasing the content of chiral agent. All of the obtained polymers showed high thermal stability.     

Combustion synthesis and photoluminescence study of silicate biomaterials

Silicate based bioceramics are promising candidates as biomaterials for tissue engineering. The combustion synthesis method provides control on the morphology and particle size of the synthesised material. This paper discusses the combustion synthesis of akermanite (Ca ₂ MgSi ₂ O ₇ and Sr ₂ MgSi ₂ O ₇ ), which has been shown to have good in vitro and in vivo bioactivities by earlier studies. Both Ca ₂ MgSi ₂ O ₇ and Sr ₂ MgSi ₂ O ₇ have akermanite structure. Ca ₂ MgSi ₂ O ₇ and Sr ₂ MgSi ₂ O ₇ were prepared using urea and ammonium nitrate. The combustion synthesis using urea and ammonium nitrate was found to be cost effective and efficient method of synthesis. The photoluminescence study of Ca ₂ MgSi ₂ O ₇ : Eu²⁺^{\boldsymbol{2+}} and Sr ₂ MgSi ₂ O ₇ : Eu²⁺^{\boldsymbol{2+}} shows host specific intense emission of Eu²⁺^{\boldsymbol{2+}}.     

Potentiometric study of polyaniline film synthesized with various dopants and composite-dopant: A comparative study

The potentiometric study of polyaniline (PANI) film synthesized with dopants viz. polyvinyl sulfonic acid (PVS),p-toluene sulfonic acid (p TS), dodecyl benzene sulfonic acid (DBS) and composite-dopants viz. PVS-p TS and PVS-DBS, has been carried out. The synthesized PANI films were characterized by electrochemical technique, UV-visible spectroscopy, Fourier transform infrared spectroscopy (FTIR), scanning electron microscope (SEM) and conductivity measurement. It was found that the PANI doped with PVS gives good electrochemical properties, conductivity as well as surface morphology as compared to p TS and DBS, whereas in composite dopants the PANI doped with PVS-pTS gives good polymer matrix as compared to PVS-DBS.     

IR and Raman spectroscopic studies of sol–gel derived alkaline-earth silicate glasses

IR and Raman spectroscopies have been utilized to study the structure and vibrational modes of sol–gel-derived binary silicate glasses. The present study is motivated by the immense geological significance and focuses on the MO–SiO ₂ (M = Ca, Mg) binary systems in an effort to unveil the role of the CaO and MgO modifiers when incorporated to the 3D silica structure. Glasses in the composition range x =0, 0·1, 0·2, 0·3 and 0·4 prepared by the sol–gel method were compared with the corresponding glasses formed by appropriate mixing of SiO ₂ and MO powders through melting and fast cooling. The vibrational spectra of the sol–gel-derived glasses have revealed considerable changes in relative intensities as a function of the MO mole fraction. These changes signify structural modifications on the silica network. The population of the Q ³ species was found to increase for both modified silicate systems. The rate of increase is more pronounced in the CaO–SiO ₂ glasses. The extent of network depolymerization in the porous glass is higher at the same content of alkaline earth oxide compared to the bulk glass. The results are indicative of a more ‘defective’ nature of the sol–gel glasses compared to the corresponding melt-quenched ones.     

Preparation and characterization of Ag-added Bi1.84Pb0.4Sr2Ca2.2Cu3O10+x bulk tube conductors for cryogen free superconducting magnet

Bulk tube conductors of Bi _1.84 Pb _0.4 Sr ₂ Ca _2.2 Cu ₃ O _10+x with addition of silver varying from 0 to 25 wt% (not reported earlier) were systematically studied using X-ray diffraction (XRD), scanning electron microscopy (SEM), electrical transport and a.c. susceptibility techniques. The tube conductors formed by cold isostatic pressing (CIP) of the powders obtained from spray drying method have been made successfully. It was found that Ag addition has not only affected the formation of the desired Bi-2223 phase and the microstructure of these large bulk tube samples thereby influencing on the critical current ( I _c ),it also reduces the contact resistance to minimize the cryogen losses. These variations have been found to be Ag content dependent. An optimized value of 10 wt% Ag has been found to produce the best quality tubes showing reproducible I _c value > 120 Amp at 77 K which is in general a requirement to energies of the cryogen free conventional/HTSC superconducting magnets below 20 K.     

Thermodynamic Characteristics of Uranyl Benzenesulfonate and p-Toluenesulfonate

The enthalpies of solution of anhydrous and hydrated uranyl benzenesulfonate (I) and p-toluenesulfonate II) in 4 M HCl were determined. The standard enthalpies of formation of I and II and their crystal hydrates from uranium trioxide, sulfonic acids, and water and enthalpies of water addition to anhydrous salts and lower hydrates of II were calculated. The enthalpy of addition of water molecule to II·H₂O is about half that of addition to II·3H₂O. With regard to all approximations in calculations, the enthalpy of formation of II from amorphous uranium trioxide and aqueous solution of the corresponding acid is by approximately 20 kJ mol^{- 1} more negative as compared to I. It was concluded that the electron-donor power of the p-toluenesulfonate ion is noticeably greater than that of the benzenesulfonate ion, which determines the difference in the properties of II and I.     

Longitudinal and transverse waves in anisotropic elastic materials

Summary It is shown that a necessary and sufficient condition for a longitudinal wave to propagate in the direction n in an anisotropic elastic material is that the elastic stiffness C ₁₁ (n) is a stationary value (maximum, minimum or saddle point) at n. Explicit expressions of all n and the corresponding elastic stiffness C ₁₁ (n) for which a longitudinal wave can propagate are presented for orthotropic, tetragonal, trigonal, hexagonal and cubic materials. As to longitudinal waves in triclinic and monoclinic materials, only few explicit expressions are possible. We also present necessary and sufficient conditions for a transverse wave to propagate in the direction n. As an illustration, explicit expressions of all n, the polarization vector a and the wave speed c for which a transverse wave can propagate in cubic and hexagonal materials are given. The search for n in hexagonal materials confirms the known fact that a transverse wave can propagate in any direction. A longitudinal wave is necessarily accompanied by two transverse waves. However, a transverse wave can propagate without being accompanied by a longitudinal wave.     

Studying the effect of particle size on the antibacterial activity of some N-nicotinyl phosphoric triamides

Using ultrasonic top-to-down method, nanoparticles of two N-nicotinyl phosphoric triamides: C₅H₄NC(O)NHP(O)R, R?=?4-CH₃-NC₅H₁₀ (1), (CH₃)₃CNH₂ (2) were prepared for the first time and characterized by ³¹P, ¹³C, ¹H NMR, FTIR, scanning electron microscopy, energy dispersive X-ray. The average particle size of 1 and 2 were 60–70 and 40–50?nm, respectively, and the morphology was spherical for 1 and rod for 2. Solid state (powder) antibacterial effect of these compounds and two other similar reported ones, in their macro- and nanosizes, were evaluated with colony counting method on one Gram-positive (Staphylococcus aureus) and one Gram-negative (Escherichia coli) bacteria in Brain–Heart infusion culture medium. Results showed that all the macro- and nanosized compounds, except macrosized 1, were antibacterial and all nanoscaled ones had stronger antibacterial activity than their macroscaled analogues. The most effect of the particle size was observed for 1: by decreasing the particle sizes, the antibacterial activity state of 1 was changed from inactive (for macro) to potent (for nano).     

Diffusivity of Al and Fe near the diffusion bonding interface of Fe3Al with low carbon steel

The distribution of elements near the Fe₃Al/Q235 diffusion bonding interface was computed by the diffusion equation as well as measured by means of EPMA. The results indicated close agreement between the two for iron and aluminium. Diffusion coefficient in the interface transition zone is larger than that in the Fe₃Al and Q235 steel at the same temperature, which is favourable to elemental diffusion. The diffusion distance near the Fe₃Al/Q235 interface increased with increasing heating temperature,T , and the holding time, t. The relation between the width of the interface transition zone,x , and the holding time,t , conformed to parabolic growth law: x bd² = 4.8 × 10⁴ exp(-133/RT) bdt -t ₀bd. The width of the interface transition zone does not increase significantly for holding times beyond 60 min.