Crystal structure and electrochemical property of one‐dimensional complex: [K(cis‐syn‐cis‐ dicyclohexyl‐18‐crown‐6)]2[Cu(mnt)2]

One metalorganic complex [K(cis‐syn‐cis‐ dicyclohexyl‐18‐crown‐6)]₂[Cu(mnt)₂] (mnt = maleonitriledithiolate) has been obtained by the reaction of dicyclohexyl‐18‐crown‐6 with K₂mnt and CuCl₂·2H₂O. The title complex has been characterized by elementary analysis, FT‐IR, UV‐Vis spectroscopy and x‐ray single crystal diffraction. The title complex crystallizes in the triclinic space group P1 with crystallographic data: a = 10.870(6) Å, b = 11.536(6) Å, c = 12.904(7) Å, α = 101.541(10)°, β = 110.573(9)°, γ = 99.441(9)°, V = 1435.2(13) ų, Z = 1, D_calcd = 1.350 g/cm³, F(000) = 615, R₁ = 0.0641, wR₂ = 0.1475. It displays one‐dimensional chain‐like structure formed by [K(cis‐syn‐cis‐ dicyclohexyl‐18‐crown‐6)]⁺ complex cations and [Cu(mnt)₂]^2‐ complex anions through N‐K‐N interactions. Its electrochemical behavior has also been studied by the cyclic voltammetry. (© 2008 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Dendritic grain growth simulation in weld molten pool based on CA‐FD model

The finite difference model is coupled with a cellular automaton (CA) model to simulate dendrite growth in TIG (tungsten inert‐gas) weld molten pool of nickel‐based alloys. Based on the macro finite difference computation of the thermal field of the whole weldment, the micro CA model is used to simulate grain formation process in 2‐dimension area within weld molten pool. The results illustrate that the complicated thermal field and solute field can lead to complex grain morphologies in weld molten pool. The primary dendrite spacing changes during welding solidification process and the final primary dendrite spacing is decided by the thermal field, solute field and other parameters. And it is indicated that the grain boundary segregation has important relationship with welding speed. The grain boundary segregations become more severe as the welding speed increases when the other parameters are kept unchanged. (© 2007 WILEY ‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Kinetic studies on the influence of temperature and growth rate history on crystal growth

Crystallization experiments of sucrose were performed in a batch crystallizer to study the effect of temperature and growth rate history on the crystal growth kinetics. In one of the growth methods adopted, the isothermal volumetric growth rate (R_V) is determined as a function of supersaturation (S) at 35, 40 and 45 ºC. In the other, crystals are allowed to grow at constant supersaturation by automatically controlling the solution temperature as the solute concentration decreased. Using the latter method R_V is calculated as the solution is cooled. The obtained results are interpreted using empirical, engineering and fundamental perspectives of crystal growth. Firstly, the overall activation energy (E_A) is determined from the empirical growth constants obtained in the isothermal method. The concept of falsified kinetics, widely used in chemical reaction engineering, is then extended to the crystal growth of sucrose in order to estimate the true activation energy (E_T) from the diffusion‐affected constant, E_A. The differences found in the isothermal and constant supersaturation methods are explained from the viewpoint of the spiral nucleation mechanism, taking into account different crystal surface properties caused by the growth rate history in each method. Finally, the crystal growth curve obtained in the batch crystallizer at 40 ºC is compared with the one obtained in a fluidized bed crystallizer at the same temperature. Apparently divergent results are explained by the effects of crystal size, hydrodynamic conditions and growth rate history on the crystallization kinetics of sucrose. (© 2008 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Synthesis,crystal growth and properties of the charge transfer complex adduct of 2‐nitro aniline with picric acid – An organic non‐linear optical material

The organic NLO material 2‐nitro aniline and picric acid (2NAP) was synthesized, needle shaped single crystals of dimension 10 × 1 × 0.8 mm^‐3 were grown by slow evaporation solution growth technique from the saturated solution of the title compound in chloroform at ambient temperature. The material was characterized through elemental analysis, powder XRD, ¹H NMR, ¹³C NMR and FTIR techniques. The various planes of reflection have been identified from the XRD powder pattern. The formation of the charge transfer complex was confirmed by UV‐VIS spectroscopy. The thermal stability of the crystals was investigated using TG/DTA analyses techniques. The second harmonic generation (SHG) efficiency of the material was estimated using Nd: YAG laser as source. (© 2008 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Study of crystalline perfection and thermal analysis of zinc cadmium thiocyanate single crystals grown in silica gel

Zinc cadmium thiocyanate ZnCd(SCN)₄ abbreviated as ZCTC is a bimetallic thiocyanate complex that exhibits excellent nonlinear optical property. Single crystals of ZCTC have been grown in silica gel by the process of diffusion. Colorless transparent crystals of size 12 mm x 2 mm x 1.3 mm have been obtained. High resolution X‐ray diffraction study was carried out to investigate the crystalline perfection of the grown crystal and the quality of the crystal was found to be quite good. Thermal stability of the grown crystal was investigated by thermogravimetric and differential thermal analyses. Fourier Transform Infrared spectrum was recorded to confirm the functional groups. Microhardness of the crystal is also studied. Being a nonlinear optical material, a comparative study of its second harmonic generation efficiency with urea has been made. (© 2007 WILEY ‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Effect of surface tension‐driven flow on BaB2O4 crystal growth from high temperature melt‐solution

The surface tension driven‐flow in BaB₂O₄ (BBO) melt‐solution is visualized by differential interference microscope coupled with Schlieren technique, and the streamline of the steady thermocapillary convection is found to be in form of an axially symmetric pattern. Based on the observation of BBO crystal rotation caused by the convective vortex, the widths of interfacial concentration, heat and momentum boundary layer are calculated. The effect of thermocapillary convection on boundary layer thickness is also investigated. Results show that the width of boundary layer decreases linearly with the increasing of dimensionless Marangoni number. (© 2008 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Optical and mechanical properties of a new second order nonlinear optical crystal urea l‐threonine

A new second order non‐linear optical organic crystal Urea L‐threonine has been grown by aqueous solution slow cooling technique. The grown crystal is non hygroscopic and transparent in the visible region. The solubility of the grown crystal was found. The crystal structure and perfection were determined using powder XRD and High resolution XRD. The molecular structure was confirmed by ¹H‐NMR spectrum. Thermal properties of the crystal have been studied using thermogravimetric (TG) and differential thermal analysis (DTA). The dielectric response of the crystal with varying frequencies at different temperatures was studied. UV‐Visible spectrum was recorded to study the optical transparency of the grown crystals. The second order non linear optical property was examined by Kurtz powder technique and found that the second order susceptibilities is 1.2 KDP at wavelength 1064 nm. The mechanical behaviour was studied by Vickers Microhardness test. The results are discussed in detail. (© 2008 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Crystal growth,crystal structure and physical properties of polar orthorhombic tris(glycine) zinc chloride

Large single crystals of the polar (point group mm 2) compound tris(glycine) zinc chloride, (NH₃CH₂COO)₃ · ZnCl₂, were grown from aqueous solutions. The refractive indices were measured in the wavelength region from 365 nm to 1083 nm and an unpolarised absorption spectrum was recorded (transparency range from 260 to 1550nm). The phase matching conditions for second harmonic generation were analysed: both, type I (ss‐f) and type II (sf‐f) are possible in the red and near IR region. All five components of the piezoelectric tensor [d_ijk ] were determined; the maximum values of longitudinal and transverse piezoelectric effects are less than one half of d₁₁₁ of α‐quartz. In addition, a redetermination of the crystal structure (including location of H atoms) is presented. (© 2008 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Crystallization of vitamin C in a continuous DT MSMPR crystallizer – Size independent growth kinetic model approach

The experimental results concerning continuous mass crystallization process in L(+)‐ascorbic acid – water system are presented and discussed. Influence of L(+)‐ascorbic acid concentration in a feeding solution and mean residence time of suspension in laboratory DT MSMPR crystallizer on product crystal size distribution as well as nucleation and growth kinetics were determined. Kinetic parameter values were evaluated on the basis of size–independent growth (SIG) kinetic model (McCabe's ΔL law). It was observed, that within the examined range of crystallizer productivity (120–1600 kg LAA crystals m^–3h^–1) crystal product population of mean size L_m from 0.2 to 0.3 mm and CV from 66.6 to 49% is withdrawn. Linear growth rate values present decreasing trend (from ca. 7 · 10^–8 to ca. 6 · 10^–8 m s^–1) with the productivity increase (assuming constant mean residence time of suspension τ = 900 s). Occurrence of secondary nucleation within the circulated and mixed suspension, resulting from crystal attrition and breakage, was observed. The parameter values in design equation connecting linear growth rate and suspension density with nucleation rate were determined. (© 2008 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Growth and characterization of nano‐crystalline hydroxyapatite at physiological conditions

Pure, stable stoichimetric nano crystalline hydroxyapatite material was crystallized by double diffusion technique at physiological conditions, temperature at 37°C and pH at 7.4. The sample was sintered at 400°C, 750°C and 1200°C with equal interval of time. They were characterized by X‐ray diffraction studies, Fourier Transformation Infra‐Red analysis, Thermogravimetric analysis, Scanning Electron Microscopic studies and Atomic Force Microscopic studies. The X‐ray analysis confirmed that the grown crystals are to be the pure form of hydroxyapatite. Infra‐red studies confirmed CO free hydroxyapatite. Thermogravimetric studies showed the thermal stability of the hydroxyapatite crystals even at 1200°C. The presence of pores in the sintered sample was traced by scanning electron microscopy. Atomic force microscopy revealed the presence of nano crystalline HAP of size 0.958 nanometer in the samples grown using this technique. At higher temperature the deagglomeration of bulk phases and agglomeration of nano phases leads to the nano crystalline HAP were observed. (© 2008 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)