Growth of octacalcium phosphate and dicalcium phosphate dihydrate crystals in silica gels

The crystallization of octacalcium phosphate (OCP) and dicalcium phosphate dihydrate (DCPD) have been studied at ambient temperature in silica gel using double diffusion system. The first stage of evolution of the OCP spherulites as well as their growth have been observed by optical microscopy. The growth rate of the OCP spherulites under stable external conditions was constant. The formation of DCPD crystals has been observed in the last stages of experiments.     

Growth of crystals of calcium sulphate in silica gel in presence of additive and their characterisation

Procedure for the growth of calcium sulphate dihydrate crystals in silica gel, in the presence of barium chloride as additive, is described. Optimum conditions for the growth of good quality crystals are worked out. The crystals are characterised by laser Raman spectroscopy, infrared spectroscopy, thermogravimetric analysis and Atomic absorption spectroscopy. It is shown that crystals in the presence of the additive have a greater degree of perfection than those without additive. Amount of water in the crystals is estimated as 20.97%. Presence of calcium and absence of barium in the crystals are indicated.     

Investigation of growth kinetics and morphology of sodium fluorosilicate ice‐analogue crystals in solutions and gels

The effect of growth method (solution or gel growth) and growth conditions on the morphology of ice analogue crystals (sodium fluorosilicate) has been studied. Many habits typical for atmospheric ice crystals (hexagonal columns, plates, different types of stars or dendrites) were obtained during experiments. The dependence of growth rate of basal and prism faces of columnar crystals on supersaturation was measured for crystals growing by evaporation of solvent. The experiments establish evaporation rate and growth rate ranges at which appearance of certain types of crystals is most probable. The experiments have also shown that good quality sodium fluorosilicate crystals can be obtained in TMS gel. These crystals were significantly bigger than those obtained in solution. (© 2007 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Growth,Structural and Microtopographical Studies of Calcium Iodate,Monohydrate Crystals Grown in Silica Gel

Single crystals of calcium iodate, monohydrate [Ca(IO₃)₂, H₂O] have been grown by gel technique. Prismatic, prismatic pyramidal, needle shaped and hopper crystals were obtained. These crystals were also grown by doping impurities such as copper and iron. Kinetics of growth parameters was investigated. Structural analysis was carried out by using X‐ray powder diffraction method. Microtopographical study of the habit faces, such as prismatic and pyramidal, of as grown crystals was carried out. Some surface structures are reported. These crystals were etched by various etchants and appropriate etchant is reported.     

Optimization of the mineral content in polymeric gels: The effect of calcium to phosphate molar ratio

The influence of calcium to phosphate (Ca/P) molar ratio on the extent of mineralization in a model (poly)acrylamide gel was investigated under simulated physiological conditions. We hypothesized that the optimal growth of hydroxyapatite crystals will take place at the stoichiometric Ca/P molar ratio of 1.67. Phosphate ions were incorporated during the polymerization of the gel and mineralization was initiated by submersion of the gel in calcium acetate solution. Ca/P molar ratios were varied in the range of 0.5–5.0. The mineralized gel was characterized by Raman spectroscopy, scanning electron microscopy (SEM) and mineral weight fraction analysis via ashing. Raman spectra captured across the bulk of the gels indicated the presence of mineral at the core section. The phosphate symmetric stretching peak was observed in the range of 955–960 cm⁻¹ which is characteristic of hydroxyapatite. SEM images showed that crystals formed at Ca/P=2.0 were denser and larger in size than at other molar ratios. In agreement with SEM images, the dry weight fraction of mineral reached the maximum at the molar ratio of 2.0 and the extent of mineralization rapidly declined as the molar ratio diverged from 2.0. Also, the crystallinity of the mineral was optimum at the molar ratio of 2.0. Thus it appears that for effective mineralization, the molar ratio of the two ions needs to be in excess of the stoichiometric requirement, suggesting that ions are expended in processes other than the formation and growth of hydroxyapatite crystals. Therefore, the optimal level of mineralization in biomimetic-based growth of calcium phosphate crystals in sol–gel environment requires consideration of a range of molar ratios as opposed to using the molar ratios corresponding to that of the crystal species intended to grow.     

Tooth enamel proteins enamelin and amelogenin cooperate to regulate the growth morphology of octacalcium phosphate crystals

To examine the hypothetical cooperative role of enamelin and amelogenin in controlling the growth morphology of enamel crystals in the post-secretory stage, we applied a cation selective membrane system for the growth of octacalcium phosphate (OCP) in the truncated recombinant porcine amelogenin (rP148) with and without the 32kDa enamelin fragment. Enamelin alone inhibited the growth in the c-axis direction more than rP148, yielding OCP crystals with the smallest aspect ratio of all conditions tested. When enamelin was added to the amelogenin "gel-like matrix", the inhibitory action of the protein mixture on the growth of OCP in the c-axis direction was diminished, while that in the b-axis direction was increased. As a result, the length to width ratio (aspect ratio) of OCP crystal was markedly increased. Addition of enamelin to amelogenin enhanced the potential of amelogenin to stabilize the amorphous calcium phosphate (ACP) transient phase. The ratio of enamelin and amelogenin was crucial for stabilization of ACP and the growth of OCP crystals with larger aspect ratio. The cooperative regulatory action of enamelin and amelogenin was attained, presumably, through co-assembling of enamelin and amelogenin. These results have important implications in understanding the growth mechanism of enamel crystals with large aspect ratio.     

FTIR spectroscopic,thermal and growth morphological studies of calcium hydrogen phosphate dihydrate crystals

Calcium hydrogen phosphate dihydrate (CHPD or DCPD) is found quite frequently in urinary calculi (stones). The CHPD crystals were grown by the single diffusion gel growth technique in sodium metasilicate gel. The crystals were found to be having platelet and broad needle type morphologies. The crystals were analyzed by FTIR spectroscopy. The thermal properties were studied by employing the thermogravimetric analysis. Various kinetic and thermodynamic parameters for dehydration were estimated. The selected platelet was studied by SEM for the growth morphologies indicating that the crystals grew in the form of leaflets having prominent (010) faces. This was in agreement with earlier reported studies. (© 2003 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Growth and characterization of pure and doped lead hydrogen phosphate single crystals in silica gel

Following the chemical reaction method pure and doped lead hydrogen phosphate single crystals were grown in silica gel using different gel density, various concentrations of phosphoric acid, and lead nitrate solutions. As the gel pH plays an important role in the formation of different H₃PO₄ species in the phosphoric acid system, the pH range in which HPO ions dominate, was considered which in turn in necessary for the growth of lead hydrogen phosphate crystals. Characteristics of these crystals were carried out by infrared spectral analysis and microhardness study.     

Numerical and experimental studies on crack formation in LiNbO3 single crystal

A global analysis of heat transfer was carried out in an inductively heated Czochralski (CZ) furnace which was actually used to grow LiNbO₃ single crystals, and then the temperature profiles obtained were used to calculate the three-dimensional thermal stress field in the crystal. By comparing the numerical results with the experimental ones, it was found that controlling the thermal environment in the CZ furnace so that the thermal stresses at the crystal surface might not exceed a certain value is important to realize the cracking free growth operation. In this study, this was accomplished through some modifications in the furnace design such as insertion of an after-heater into the furnace. These findings were verified by additional numerical simulations and crystal growth experiments for some growth conditions.     

Gel growth of α and γ glycine and their characterization

The microbial free single crystals of α and γ glycine were grown from gel at room temperature in a new chemical route. These crystals showed a superior quality than the solution grown crystals. The metastable α-form and the stable γ-form of glycine were crystallized in silica gel by solubility reduction method. The form of crystallization is confirmed by single crystal and powder X-ray diffraction analyses. The crystals of α and γ glycine were found to crystallize in monoclinic and hexagonal crystal systems, respectively. For analyzing the functional group and thermal stability of α and γ glycine crystals, spectroscopic and thermal analyses have been carried out. The dielectric studies were performed to find the dielectric constant of the grown crystals and the results are discussed. Second harmonic generation efficiency of the crystal was measured by Kurtz’s powder method using Nd:YAG laser and it was found to be 2.68 times that of potassium dihydrogen phosphate crystals.     

Spectroscopic, thermal and structural studies on manganous malate crystals

Prismatic crystals of manganous malate have been prepared by controlled ionic diffusion in hydrosilica gel. The structure was elucidated using single crystal X-ray diffraction. The crystals are orthorhombic with space group Pbca. Vibrations of the functional groups were identified by the FTIR spectrum. Thermogravimetric and differential thermal analyses (TG-DTA) were carried out to explore the thermal decomposition pattern of the material. Structural information derived from FTIR and TG-DTA studies is in conformity with the single crystal XRD data.     

Growth and microstructural studies of some indium chalcopyrite semiconductors

Single crystals of ternary chalcopyrite semiconductors such as CuInS₂, CuInSe₂, CuInTe₂, and CuInSSe, a pseudo-ternary semiconductor, have been grown by Chemical Vapour Transport (CVT) technique using iodine as the transporting agent. Microstructural analysis was carried out with the help of Scanning Electron Microscope (SEM) and optical microscope for the grown single crystals.     

The mechanism of biological mineralization

The control of supersaturation and the nucleation and growth of crystals in calcium phosphate systems are important in relation to the physiological deposition of bone and tooth. Other calcium salts such as the carbonate and oxalate hydrates are significant components of pathological mineral deposits. The use of a highly reproducible seeded growth technique has enabled kinetic studies to be made of the crystal growth of these minerals. Under conditions of relatively high supersaturation, secondary nucleation may be induced upon the surface of the seed crystals. In the case of the calcium phosphates, temperature, supersaturation, surface concentration, pH, ionic strength and presence of foreign ions are very important in determining the nature of the phase which grows upon the added seed crystals. Kinetic considerations are of overriding importance in determining the course of the reactions. It is not possible to predict the phase which forms purely on the basis of thermodynamic solubility data. Thus, in solutions appreciably supersaturated with respect to both dicalcium phosphate dihydrate (DCPD) and hydroxyapatite (HAP), the addition of low concentrations of HAP seed results in the exclusive formation of DCPD whereas this phase is absent when the seed concentration is increased. The kinetic results for calcium oxalate and phosphates are discussed in terms of the important problems relating to tooth mineralization and the origin and growth of renal calculi.     

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.     

XRD,thermal and FTIR studies on gel grown DL‐Phenylalanine crystals

Phenylalanine [C₉H₁₁NO₂] is one of the essential amino acids in humans. DL‐phenylalanine was crystallized in silica gel under suitable pH conditions by reduction of solubility method. The grown crystals were characterized by density measurement and X‐ray powder diffraction. Fourier transform infrared spectroscopy, and thermogravimetric analysis were also carried out. (© 2007 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

The Influence of the Hydrodynamic Environment on the Growth and the Formation of Liquid Inclusions in Large Potassium Dihydrogen Phosphate (KDP) Crystals

The influence of the hydrodynamic environment on the growth phenomena of large potassium dihydrogen phosphate (KDP) crystals has been investigated in a three vessel system. Special attention was paid to the onset of inclusion formation. Flow visualization experiments carried out in a wind tunnel showed that the flow formed at the rear (downstream) faces of the crystal (i.e. the wake) is a more or less closed circulation system. It appeared that veils of liquid inclusions are not a result of starvation in the laminar boundary layer, as suggested before, but of depletion in the closed wake at the rear.     

Effect of phosphonate additive on crystallization of gypsum in phosphoric and sulfuric acid medium

Understanding the mechanisms of growth and inhibition during crystallization of calcium sulfate is of primary importance for many industrial applications. For instance, inhibition of the crystallization process may be required to prevent scale formation in pipes, boilers, heat exchangers, reactors, reverse osmosis membrane surfaces, cooling water systems, secondary oil recovery utilizing water flooding techniques and desalination evaporators, etc. On the other hand, control growth and morphology of gypsum crystals is desired in achieving higher filtration rate and higher productivity of phosphoric acid from phosphate rocks. In this regard, this basic study is carried out to understand effect of Aminotris (methylenephosphonic acid (ATMP) on calcium sulfate dihydrate (gypsum) crystallization. The time elapsed between the achievement of supersaturation and the appearance of a solid phase (termed as induction time) is measured under different supersaturation ratios ranging from 1.018 to 1.979. The data are used to calculate the surface energy, critical nucleus size, and crystal growth rates of gypsum under different conditions. The results show that, the induction time decreases exponentially with increasing the supersaturation ratio. In addition, the surface energy decreases with ATMP compared to the baseline (without ATMP). Interestingly, with addition of the ATMP, the crystals mean and median diameters are found to decrease. The inhibition efficiency ranges from 16% to 59% depending on supersaturation ratio.     

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)     

A study of primary nucleation of calcium oxalate monohydrate: II. Effect of urinary species

Kidney stones consist of various organic and inorganic compounds. Calcium oxalate monohydrate (COM) is the main inorganic constituent of kidney stones. However, the mechanisms for the formation of calcium oxalate kidney stones are not well understood. In this regard, there are several hypotheses including nucleation, crystal growth and/or aggregation of formed COM crystals. The effect of some urinary species such as oxalate, calcium, citrate, and protein on nucleation and crystallization characteristics of COM is determined by measuring the weight of formed crystals and their size distributions under different chemical conditions, which simulate the urinary environment. Statistical experimental designs are used to determine the interaction effects among various factors. The data clearly show that oxalate and calcium promote nucleation and crystallization of COM. This is attributed to formation of a thermodynamically stable calcium oxalate monohydrate resulting from supersaturation. Citrate, however, inhibits nucleation and further crystal growth. These results are explained on the basis of the high affinity of citrate to combine with calcium to form soluble calcium citrate complexes. Thus, citrate competes with oxalate ion for binding to calcium cations. These conditions decrease the amount of free calcium ions available to form calcium oxalate crystals. In case of protein (mucin), however, the results suggest that no significant effect could be measured of mucin on nucleation and crystal growth. (© 2004 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

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)