Synthesis and characterization of monetite and hydroxyapatite whiskers obtained by a hydrothermal method

High temperature hydrothermal syntheses, using calcium nitrate tetrahydrate, sodium dihydrogen phosphate and urea as precursors, and characterization of hydroxyapatite (HAp) whiskers are reported herein. The morphology and chemical composition of the crystals from a monetite to a hydroxyapatite phase were controlled by varying the starting concentrations of the precursors and the solution pH through the amount of urea that is decomposed during heating. X-ray diffraction (XRD) analysis, infrared spectroscopy (IR), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), transmission electron microscopy (TEM) and high-resolution TEM (HRTEM) were used to investigate the products of the syntheses in order to find the optimum reaction conditions for obtaining the desired morphology and phase composition. Different morphologies ranging from single crystals of monetite through rods and plates of hydroxyapatite with different size distribution to whisker-like single hydroxyapatite crystal were achieved by simply varying the starting concentration of urea. Structural refinement of the hydroxyapatite whiskers confirmed a strong preferential orientation along the c-axis direction of the hexagonal crystal structure, which was significantly different from the usually observed random crystal orientation. TEM and SEM analysis of the apatite whiskers confirmed single crystal structure with the a c-axis orientation parallel to the long axis of the whiskers, with sizes up to 150 μm in length, 10 μm in width and with a thickness of about 300 nm, that grew from the same centre of nucleation, forming flaky-like particles.     

Derivation and validation of a binary multi-fluid Eulerian model for fluidized beds

The paper presents a multi-fluid Eulerian model derived from binary kinetic theory of granular flows, free path theory and an empirical friction theory. The effects of the inter- and inner-particle collisions, particle translational motions and particle–particle friction are included. As the effects due to fluiddynamic particle velocity differences and particle–particle friction are considered, some unconventional terms are produced compared with the previous models. Model validation using the data from Mathiesen et al. (2000) shows that the coupling terms give a stronger and more realistic particle–particle coupling because the effects due to the fluiddynamic velocity differences are considered. The model gives reasonable predictions of the particle volume fraction, particle velocities and velocity fluctuations. The model analysis reveals that the basic particle velocity fluctuations constitute 2 terms: the velocity fluctuations of the discrete particles, and the velocity fluctuations of the continuous fluid flow. Furthermore, the simulation results show that the velocity fluctuations of the continuous fluid flow are dominant in a binary riser flow.     

Effect of propylation on the characteristics of corn starch and variation of properties with different degrees of substitution

Corn starch was modified by propylation with different degree of substitution (DS). DS of four starch modifications were 0.61, 1.56, 2.27, and 2.51. Samples were characterized by FTIR, XRD, TG‐DTA, swelling power, solubility, water binding capacity, and light transmittance. Results of the systematic physico‐chemical characterization of the starch modification in comparison with the native starch have been documented in the article. Results showed that during propylation, the crystalline structure of starch got destroyed and surface of the starch was eroded. Propylated starch (DS 2.51) showed 85% weight loss at temperatures from 300 to 400°C, whereas the native starch underwent similar weight loss (83%) from 250 to 300°C. Swelling power and water binding capacity of native starch (DS 0.0) were 3.09 g/g and 89.8%, respectively. However, in propylated starch at low DS (DS 0.61), swelling power and water binding capacity increased to 10.55 g/g and 136.8% under same conditions. At high DS (DS 2.51), swelling power was similar to native starch at 65°C, whereas solubility and water binding capacity decreased to below that of native starch. Light transmittance of propylated starch with high DS (DS 2.51) increased dramatically compared with native starch. Propylation improved the hydrophobic transformation and thermal stability of starch at high DS. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

An Experimental Workflow for Studying Barrier Integrity,Permeability, and Tight Junction Composition and Localization in a Single Endothelial Cell Monolayer: Proof of Concept

Endothelial and epithelial barrier function is crucial for the maintenance of physiological processes. The barrier paracellular permeability depends on the composition and spatial distribution of the cell-to-cell tight junctions (TJ). Here, we provide an experimental workflow that yields several layers of physiological data in the setting of a single endothelial cell monolayer. Human umbilical vein endothelial cells were grown on Transwell filters. Transendothelial electrical resistance (TER) and 10 kDa FITC dextran flux were measured using Alanyl-Glutamine (AlaGln) as a paracellular barrier modulator. Single monolayers were immunolabelled for Zonula Occludens-1 (ZO-1) and Claudin-5 (CLDN5) and used for automated immunofluorescence imaging. Finally, the same monolayers were used for single molecule localization microscopy (SMLM) of ZO-1 and CLDN5 at the nanoscale for spatial clustering analysis. The TER increased and the paracellular dextran flux decreased after the application of AlaGln and these functional changes of the monolayer were mediated by an increase in the ZO-1 and CLDN5 abundance in the cell–cell interface. At the nanoscale level, the functional and protein abundance data were accompanied by non-random increased clustering of CLDN5. Our experimental workflow provides multiple data from a single monolayer and has wide applicability in the setting of paracellular studies in endothelia and epithelia.     

Measurement of surface‐transfer coefficient values for CO2 absorption in lime solutions in presence of surfactants

A modified manometric apparatus has been used for the experimental determination of surface‐transfer coefficient values, used for the design calculations of various mass‐transfer equipments, for the absorption of carbon‐dioxide gas in saturated lime solution in presence of different types of surfactants. An analytical expression has been derived for estimation of the volume of gas absorbed, using the manometric data, for different times of absorption. The rate of gas absorption was found to remain constant initially for about 1 min and thereafter decreased with the progress of absorption time. Surface‐transfer coefficient values for gas absorption have been calculated using the experimental data of the volume of gas absorbed, without and with the addition of different concentrations of surfactants to the lime solutions. For a particular surfactant, surface‐transfer coefficient values were found to decrease with an increase in the concentration of surfactant in solution. The calculated values of the surface‐transfer coefficients for different surfactants are in close agreement with those reported in the literature.     

Inference about long run canonical correlations

This article proposes methods for testing the null hypothesis that a number of so‐called long run canonical correlations (LRCCs) are zero. Two test statistics are proposed and their limiting distributions are derived under the null hypothesis. The finite sample properties of the tests are illustrated via a number of simulation studies that reveal the asymptotic theory provides a good guidance to behaviour in moderate or large sized samples. It is shown that the statistics provide a natural way for testing the asymptotic independence of two standardized sums. The usefulness of the tests is illustrated via the following examples: inference about cointegrating vector in a particular cointegration model; inference about break points in a cointegration model; moment estimation; parameter estimation in Generalized Method of Moments estimation.     

The effect of lignin on the structure and characteristics of composite coatings electrodeposited on titanium

Composite coatings based on lignin, obtained by electrophoretic deposition (EPD) on titanium, were investigated. The aim of this work was to produce hydroxyapatite/lignin (HAP/Lig) coatings on titanium and to investigate the effect of the lignin concentration on microstructure, morphology, phase composition, thermal behavior and cytotoxicity of the HAP/Lig coatings. An organosolv lignin was used for the production of the composite coatings studied in this research. The properties of HAP/Lig coatings were characterized using X-ray diffraction (XRD) analysis, scanning electron microscopy (SEM), thermogravimetric analysis (TGA), attenuated total reflection Fourier transform infrared spectroscopy (ATR-FT-IR) and X-ray photoelectron spectroscopy (XPS), as well as the MTT test of cytotoxicity. The results showed that higher lignin concentrations protected the HAP lattice during sintering, thereby improving the stability of the HAP/Lig coatings. The cell survival of peripheral blood mononuclear cells (PBMC) after proliferation indicates that the HAP/Lig coating with 1 wt% Lig electrodeposited on titanium was non-toxic with significant promise as a potential bone-repair material.     

3D Coordination Network of Ag(I) Ions with μ 3 -Bridging Melamine Ligands

Abstract  

A new 3D silver complex [Ag(mela)(H₂O)(NO₃)]_n (1) (mela = melamine or 2,4,6-triaminotriazine) is synthesized and characterized by single crystal X-ray diffraction, IR, and elemental analysis. The structural characterization shows that the compound crystallizes in space group C c, a = 8.181(2), b = 10.269(3) c = 11.347(3) ?, β = 105.88(2)°, Z = 4. Out of several structurally characterized transition metal compounds comprising melamine, the titled complex represents a rare example of μ ₃ -melamine coordination mode realized through the heterocycle nitrogen donors. The fluorescent property of complex 1 was investigated and the mechanism was validated by means of a density functional theory (DFT) calculation.     

Solubility parameter estimation and phase inversion modeling of bentonite-doped polymeric membrane systems

Effects of bentonite concentration on morphology and permeation characteristics of bentonite-doped polysulfone membranes were investigated. Solubility sphere for bentonite was constructed to estimate its solubility parameter. Thermodynamic modeling of phase inversion of this system was carried out using Flory–Huggins theory. The trade-off between thermodynamic and kinetic parameters was used to predict the membrane morphology for bentonite concentration varying from 0 to 5 wt %. The porosity of bentonite-doped membranes decreased up to 3 wt % that increased thereafter. Morphological analysis showed dense cross section with finger-like macrovoids at 3 wt % beyond which it changed to honeycomb structure with large circular voids. Permeability of 3 wt % membrane was the lowest (5.6 × 10⁻¹² m/Pa s) with 95% bovine serum albumin rejection. Contact angle of the membranes decreased from 83 to 66° with bentonite addition making the membrane more hydrophilic. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48450.