Growth of single crystals of barium iodate and strontium iodate in silica gels

Single crystals of iodates of barium and strontium grown by gel method are reported. Optimum conditions for good quality single crystals are worked out. Different habits of these crystals are reported. A brief report for characterization of these crystals by different methods is given.     

Growth of calcium oxalate crystals induced by complex films containing biomolecules

Nucleation and growth of calcium oxalate (CaC₂O₄) crystals induced by films composed of phosphatidylcholine (PC), cholesterol (CS) and human serum albumin (HSA), and of PC, CS and dextran have been carried out. The products obtained were characterized by Fourier transform infrared spectroscopy, scanning electron microscopy and ultraviolet‐visible spectroscopy. The results indicate that hexagonal calcium oxalate monohydrate (COM) and club‐shaped calcium oxalate trihydrate (COT) crystals are obtained on the PC/CH/HSA film, and the microstructure and properties of the PC/CH/HSA film depend on the weight ratio of PC to CS. With an increase in the PC‐to‐CS ratio, the number of COM crystals decreases gradually, and finally disappear, suggesting that PC inhibits the growth of COM crystals. On the PC/CS/dextran film, irregular COM and COT crystals are formed. The possible formation mechanisms of CaC₂O₄ on the two complex films are discussed. (© 2007 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Growth of calcium phosphate crystals in Silica gel

The results of a study of the crystal growth of calcium phosphates in silica gel employing double diffusion system with CaCl₂ and KH₂PO₄ aqueous solutions are reported. Liesegang rings, spherical crystalline agglomerates and brushite dendrites are formed near the CaCl₂ solution. It was found that the agglomerates consist of octacalcium phosphate and hydroxyapatite crystals with the predominance the former.     

Growth of hierarchical calcium carbonate crystals templated by biomolecules of lotus root

In this paper, crystal growth of calcium carbonate (CaCO₃) in the presence of biomolecules of lotus root was investigated. Scanning electron microscopy, Fourier transform infrared spectroscopy and X‐ray powder diffractometry were used to characterize the products. The results indicate that calcite spherical particles were constructed from small rhombohedral subunits. Similar CaCO₃ crystals were also gained when crystal growth of CaCO₃ in aqueous solution containing extracts of lotus root was performed, suggesting that the soluble biomolecules of lotus root play a crucial role in directing the formation of hierarchical calcite spherical particles. The possible formation mechanism of the CaCO₃ crystals by using lotus root is also discussed, which can be interpreted by particle‐aggregation based non‐classical crystallization laws. The biomolecules of lotus root might induce and control the nucleation and growth of calcium carbonate crystals. (© 2009 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Growth of LGSO: Ce crystals by the Czochralski method

Single crystals of Lu_2x Gd_{2 ? 2x} SiO₅: Ce (0 < x < 1) compounds with different atomic ratios Lu/(Lu + Gd) have been grown by the Czochralski method. It has been shown that a change in the spatial symmetry from P2₁/c to C2/c in the course of substitution of lutetium for gadolinium occurs at the ratio Lu/(Lu + Gd) = 0.1. The lattice thus formed with symmetry C2/c in the structure of Lu_2x Gd_{2 ? 2x} SiO₅: Ce crystals favors the maximum possible incorporation of Ce³⁺ ions into the sevenfold-coordinated position with respect to oxygen. This explains the substantial improvement of the scintillation characteristics of the grown crystals.     

Growth of CdSiP2 single crystals by self-seeding vertical Bridgman method

Using a high purity CdSiP₂ polycrystalline charge synthesized in a single-temperature zone furnace, a CdSiP₂ single crystal with dimensions of 8 mm in diameter and 40 mm in length was successfully grown by the vertical Bridgman method. The quality of the crystal was characterized by high resolution X-ray diffraction and the full width at half maximum (FWHM) of the rocking curve for the (200) face is 33″. Thermal property measurements show that: the mean specific heat of CdSiP₂ between 300 and 773 K is 0.476 J g^?1 K^?1; the thermal conductivity of the crystal along the a- and c-axes is 13.6 W m^?1 K^?1 and 13.7 W m^?1 K^?1 at 295 K, respectively; and the thermal expansion coefficient measured along the a- and c-axes is 8.4×10^?6 K^?1 and ?2.4×10^?6 K^?1, respectively. The optical transparency range of the crystal is 578–10,000 nm, and there is no absorption loss in the spectrum from 0.7 to 2.5 μm, as often exists with ZnGeP₂ crystals grown from the melt.     

Growth of p-type InP single crystals by the temperature gradient method

P-type InP single crystals doped with zinc or cadmium have been prepared from a solution using indium as a solvent in which a temperature gradient was maintained for the transport of the InP solute. The average growth rate was between 1.1 and 3.0 mm/week. The room temperature hole concentration of the crystals obtained was in a range of 10¹⁷ to 10¹⁸ cm^-3. The distribution coefficients of zinc and cadmium were 0.8 and 0.004, respectively. The temperature gradient method makes it possible to dope the crystals with volatile impurities in a controlled manner.     

Growth of cobalt single crystals by the Electron beam floating-zone method

Co single crystals of striation-free were grown easily by the electron-beam floating-zone melting. For these crystals, observations on dislocations were carried out. Slight preferred direction of grown crystals were discussed on the basis of the local step structure on the crystal surface.     

Growth and characterization of gel grown calcium pyrophosphate tetrahydrate crystals

Formation of calcium pyrophosphate dihydrate (CPPD) crystals in soft tissues such as cartilage, meniscus and synovial tissues lead afflictions. The appearance of these crystals in the synovial fluid give rise to acute arthritis attack, which is known as pseudo‐gout. The growth of calcium pyrophosphate crystals in gel medium can mimic the growth in a body. In the present study, calcium pyrophosphate tetrahydrate (CPPT) crystals are grown by a single diffusion gel growth technique and characterized by powder XRD, FT‐IR spectroscopy, TGA, kinetic and thermodynamic studies of dehydration and dielectric studies. Monoclinic crystals structure, presence of P‐O bonds and four water molecules are confirmed from powder XRD, FT‐IR and TGA studies, respectively. The dielectric investigation suggests the reduction in dielectric constant with increase in frequency. (© 2007 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Growth of high-purity ZnTe single crystals by the sublimation travelling heater method

A travelling heater method (THM) was developed to grow high-purity ZnTe from the vapor phase. This crystal growth method is called the “sublimation THM”. The temperature of the sublimation interface was set at 815°C and the temperature of the growth interface was varied from 785 to 800°C. The growth rate was 3 mm/day. Under these conditions, it was found that the growth process was mainly due to surface nucleation. Characteristics of the crystals were compared with those of solution-THM and vapor phase epitaxially grown crystals. The free-exciton line at 2.381 eV strongly appears and a doublet structure in neutral- acceptor bound exciton at 2.375 eV is clearly resolved with splitting energy of about 0.7 meV. We thus conclude that the THM from the vapor phase is suitable for preparing ZnTe single crystals which have excellent luminescent properties.     

Growth and characterization of CdSe single crystals by modified vertical vapor phase method

Good quality, large single crystals of CdSe were grown by the modified growth method (i.e., vertical unseeded vapor phase growth with multi-step purification of the starting material in the same quartz ampoule without any manual transfer between the steps). Lower temperature gradients (8–9°C/cm) at the growth interface were used for the crystal growth. As-grown CdSe crystals was characterized by X-ray diffraction, scanning electron microscopy, energy dispersive analyzer of X-rays, high-resistance instrument measurement, and etch-pit observation. It is found that there are two cleavage faces of (1 0 0) and (1 1 0) orientations on the crystal, the resistivity is about 10⁸ Ω cm, and the density of etch pits is about 10^3–4/cm². The crystal was cut into wafers and was fabricated into detectors. The detectors were tested using an ²⁴¹Am radiation source. γ-ray spectra at 59.5 keV were obtained. The results demonstrated that the quality of the as-grown crystals was good. The crystals were useful for fabrication of room-temperature-operating nuclear radiation detectors. Therefore, the modified growth technique is a promising, convenient, new method for the growth of high-quality CdSe single crystals.     

Growth of calcium oxalate monohydrate on uric acid crystals at sustained supersaturation

The effect of uric acid seeds on calcium oxalate formation was studied at pH 4.50 and 37 °C using a system providing constant supersaturation with respect to calcium oxalate and saturated in uric acid. In all cases the only solid‐phase forming was identified as calcium oxalate monohydrate (COM). Kinetic analysis of the initial rates showed that they were proportional with the relative supersaturation with respect to calcium oxalate monohydrate. The linear dependence of the rate of precipitation of COM on uric acid suggested that growth is mediated through a surface diffusion controlled mechanism. (© 2004 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Growth of 2-methyl-4-nitroaniline (MNA) crystals by the bridgman method

Organic single crystals of 2-methyl-4-nitroaniline (MNA) up to 3 mm in diameter and 20 mm in length have been successfully grown by the Bridgman method using the purified reagent by sublimation. The crystals are transparent and yellow in colour by controlling the growth conditions. In the spectra of yellow coloured crystals no absorption peak is observed until about 450 nm. Also, the crystals of MNA have the two cleavage planes (311 ) and (010).     

Growth of borax crystals by spiral mechanism

Borax crystals grown at low supersaturation values are described. A brief report about microtopographical studies of these crystals is presented. Growth spirals observed on almost all the habit faces except those in contact with the bottom of the nucleation cell are described and discussed. It is established that all these crystals have platelet form in the initial stages of crystallization and as growth proceeds they develop and grow by spiral mechanism. The conditions under which the screw dislocations play the role in the development and growth of the crystals have been worked out.     

Growth of single crystals of semiconductor solid solutions by double feeding of the melt method

Crystallography Reports - The problem of component distribution in solid solution crystals grown from a melt fed by rods made of the components of the system, with allowance for the dependence of...     

Growth of Potassium Sulphate Crystals by Silica Gel Technique

Single and transparent crystals of potassium sulphate up to 30 × 3 × 3 mm in size have been grown by silica gel technique, using various methods (two-layers three-layers and hybrid gel technique) which are described. The effects of the three differents alcohols (used as top solutions) upon the quality and nucleation of crystals are also reported. The “growth and equilibrium” morphologies and microstructures of the habit faces are discussed.     

Growth and characterization of calcium hydrogen phosphate dihydrate crystals from single diffusion gel technique

Calcium hydrogen phosphate dihydrate (CaHPO₄·2H₂O, CHPD) a dissolved mineral in urine is known to cause renal or bladder stones in both human and animals. Growth of CHPD or brushite using sodium metasilicate gel techniques followed by light and polarizing microscopic studies revealed its structural and morphological details. Crystal identity by powder x‐ray diffraction confirmed the FT‐IR and FT‐Raman spectroscopic techniques as alternate methods for fast analysis of brushite crystals which could form as one type of renal stones. P‐O‐P asymmetric stretchings in both FT‐IR (987.2, 874.1 and 792 cm^‐1) and FT‐Raman (986.3 cm^‐1, 1057.6 cm^‐1 and 875.2 cm^‐1) were found as characteristics of brushite crystals. Differential Scanning Calorimetry (DSC) analysis revealed brushite crystallization purity using gel method by studying their endothermic peaks. This study incorporated a multidisciplinary approach in characterizing CHPD crystals grown in vitro to help formulate prevention or dissolution strategy in controlling urinary stone growth. Initial studies with 0.2 M citric acid ions as controlling agent in the nucleation of brushite crystals further support the presented approach. (© 2010 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)