Effect of silicon and heat-treatment temperature on the morphology and mechanical properties of silicon - substituted hydroxyapatite

The precipitation method was used to synthesize silicon-substituted hydroxyapatite with different Si contents of 0.4, 0.8 and 1.6 wt.% (0.4, 0.8 and 1.6Si-HA) using silicon acetate [Si(OCOCH₃)₄] as a Si source. As-synthesized hydroxyapatite (HA) and Si-HA powders/bulks were heat-treated at different temperatures of 1150, 1200 and 1250 °C for 1 h. Pure 0.4Si-HA and 1.6Si-HA were obtained after heat-treatment at all temperatures, whilst α-TCP phase was formed in the 0.8Si-HA sample after heat-treatment at 1250 °C. SEM observation clearly showed that the substitution of Si in HA inhibited the grain growth of Si-HA even at high heat-treatment temperatures (1200 or 1250 °C). The highest diametral tensile strength (DTS) of 15.93 MPa was obtained in the 1.6Si-HA sample after heat-treatment at 1250 °C.     

Synthesis and characterization of 5,7-dimethyl-8-hydroxyquinoline and 2-(2-pyridyl)benzimidazole complexes of zinc(II) for optoelectronic application

Bis(5,7-dimethyl-8-hydroxyquinolinato)zinc(II) (Me₂q)₂Zn and 5,7-dimethyl-8-hydroxyquinolinato(2-(2-pyridyl)benzimidazole) zinc(II) Me₂q(pbi)Zn have been synthesized and characterized by various techniques. These metal complexes have high thermal stability (>300 °C) and high glass transition temperatures (>150 °C). The vacuum deposited films of these materials show good film forming property and are suitable for opto-electronic applications. Multilayered organic electroluminescent (EL) devices have been fabricated having structure ITO/α-NPD/zinc complex/BCP/Alq₃/LiF/Al, which produce emission with chromaticity having Commission Internationale d’Eclairage (CIE) coordinates x = 0.506 and y = 0.484 for (Me₂q)₂Zn; x = 0.47 and y = 0.52 for (Me₂q)(pbi)Zn complex. The electroluminescence spectra show peak emission centered at 572 and 561 nm respectively for these materials.     

Effect of Stilling Basin Geometry on Clear Water Scour Morphology Downstream of a Block Ramp

The scour mechanism downstream of a block ramp in clear water conditions is quite a complex phenomenon that depends on several parameters. Majors role are played by ramp configuration, hydraulic conditions (downstream tailwater level and discharge), material granulometry, and stilling basin geometry. Previous studies analyzed both the scour phenomenon and the effects of all the parameters involved except the last one (i.e., the case in which the ramp has the same width as the downstream stilling basin) and the case of symmetrically expanding stilling basins. This last basin configuration represents an optimal equilibrium between the necessity to dissipate energy and to create a natural pool for the biological species, thus it has a prominent ecological value. The present paper aims to assess the effect of both the width and length of the downstream stilling basin on scour features and flow pattern in clear water conditions. Different scour morphology types are distinguished and classified according to hydraulic and geometric conditions. Simple novel relationships are proposed to evaluate the scour depth and length and the maximum water level in the stilling basin. The results are valid for unsubmerged block ramps.     

Regime Equations for Natural Meandering Cobble- and Gravel-Bed Rivers

Data obtained from 48 stable reaches of upland rivers in the UK were stratified by stream type to develop regime equations specifically for natural meandering cobble- and gravel-bed rivers: C3 and C4 stream types, according to the Rosgen classification. Multiple regression models were applied to derive equations for reach-averaged values of bankfull width, mean depth, slope, meander arc length and sinuosity in bankfull discharge and associated bed-material load, the caliber of the bed material, bank vegetation density, and valley slope. The equations show that their cross-sectional dimensions are primarily determined by the bankfull discharge, bank vegetation, and bed-material size, whereas their profile and plan form are very strongly influenced by the valley gradient. Although bankfull bed-material load only appears to have a minor influence on channel morphology, its effect is implicit in the value of bankfull discharge because this corresponds to the flow that transports most of the bed-material load. Explanations are given for these results on the basis of processes affecting channel geometry. Comparisons with the regime equations derived more than 20?years ago by Hey and Thorne from the same UK data set indicate that stratification by stream type generates equations that are more consistent; for example, bank vegetation affects all aspects of channel morphology rather than simply channel width, and provides significantly better explanations for channel slope and sinuosity because of the inclusion of valley slope as an independent variable. Their potential for designing river restoration schemes is evaluated against North American data. The equations prove to be comparable to the Hey and Thorne equations for predicting width and depth, but provide a significant improvement for the determination of slope and sinuosity. Although bed-material load was shown, statistically, to influence channel dimensions, numerically its influence is trivial. Removing it from the analysis generates equations that provide the best practical point estimates of channel morphology. Predictions with the simplified regime equations are shown to be comparable to the full equations.     

Effect of mixed solvents on PCDTBT:PC70BM based solar cells

We investigated the effect of solvents on the morphology, charge transport and device performance of poly[N-9″-hepta-decanyl-2,7-carbazole-alt-5,5-(4′,7′-di-2-thienyl-2′,1′,3′-benzothiadiazole)] (PCDTBT) and [6,6]-phenyl C71-butyric acid methyl ester (PC₇₀BM) based solar cells. To carry out this investigation, chloroform and 1,2-dichlorobenzene were chosen as good solvents of the two compounds. Films prepared with chloroform exhibit larger domains than those prepared with 1,2-dichlorobenzene and their size increases with the amount of PC₇₀BM. Fine tuning of the domain size was realized by using a solvent of mixed chloroform and 1,2-dichlorobenzene. At a mixing ratio of 50%:50%, a power conversion efficiency of 6.1% was achieved on PCDTBT:PC₇₀BM (1:3) devices with an active area of 1 cm², under air mass 1.5 global (AM 1.5 G) irradiation at 100 mW/cm².     

Hydrophilic modification of P(VDF-co-CTFE) porous membranes

This paper describes fabrication of a poly(vinylidene difluoride-co-chlorotrifluoroethylene) (P(VDF-co-CTFE)) porous membrane via non-solvent induced phase inversion and subsequent hydrophilic modification using high efficient surface initiated atom transfer radical polymerization (ATRP). The effect of viscosities of casting solutions on microstructures of the P(VDF-co-CTFE) membrane was investigated. The surface chemistry, thermal stability, morphological structure, and hydrophilicity of the modified membranes were evaluated by Fourier Transform Infrared Attenuated Total Reflection (FTIR-ATR), Differential Scanning Calorimeter (DSC), Scanning Electron Microscope (SEM), and contact angle measurements, respectively. The degree of grafting and the degree of swelling were measured to analyze the effect of polymerization time on the wettability. The mechanical strength of the membranes after modification was also investigated. The permeability and fouling resistance were evaluated according to pure water flux and protein solution filtration measurements. The results demonstrate that the hydrophobic P(VDF-co-CTFE) membrane can be feasibly modified by immobilization of hydrophilic poly(ethylene glycol) methyl ether methacrylate (PEGMA) brushes via surface initiated ATRP.     

Correlations between water uptake and effective fixed charge concentration at high univalent electrolyte concentrations in sulfonated polymer cation-exchange membranes with different morphology

Water uptakes properties and effective fixed charge concentration have been determined in aqueous electrolyte solutions (LiCl, NaCl and KCl) for different commercial sulfonated polymer cation-exchange membranes with different morphology. Differences in the water uptake properties and in the membrane effective fixed charge concentration has been found, which have been analyzed on the basis of the different membrane structures. The experimental results show correlations between the water uptake and the loss of the membrane selectivity at high electrolyte concentrations which are dependent on the membrane morphology. Relationships are found which permit to estimate the membrane effective fixed charge concentration from equilibrium and morphological properties with the advantage of avoiding the need for membrane potential measurements.     

AFM investigation of solid product layers of MgSO4 generated on MgO surfaces for the reaction of MgO with SO2 and O2

The nucleation, growth and arrangement of MgSO₄ product layers during the reaction of single-crystal MgO with SO₂ and O₂ were investigated via atomic force microscopy (AFM). The morphology of the single-crystal MgO surface after reacting with SO₂ and O₂ consisted of three-dimensional cone-shaped MgSO₄ product islands. Most of the islands appeared at locations with terraces, steps and kinks. With increasing reaction time, small product islands grew to large islands, finally coalescing into continuous islands. The nucleation, growth and arrangement of the solid products on the reactant surface are controlled by thermodynamics and kinetics. The morphology of the MgSO₄ product islands is governed by the competition between the intrinsic chemical reaction rate and the product molecular diffusion rate, which are both significantly affected by the reaction temperature. As the reaction temperature increases, the mean size of the MgSO₄ islands increases while the island density decreases. The nucleation, growth and arrangement of the solid product layers and the product layer morphology on the solid reactant surface directly affect the mechanism of the gas–solid reaction.     

Advanced chemically induced phase separation in thermosets: Polybenzoxazines toughened with multifunctional thermoplastic main-chain benzoxazine prepolymers

Multifunctional thermoplastic main-chain benzoxazine prepolymers were synthesized and systematically varied in their structure in order to function as high-performance toughener additives. Their unique chemical composition allows multiple covalent crosslinking with many thermoset network systems including benzoxazines and epoxides in conjunction with a defined chemical induced phase separation (CIPS) upon curing. This was successfully shown using a benzoxazine-based thermoset resin matrix as an example. The corresponding morphologies were addressable in a predictable manner and brought into context with the obtained macroscopic mechanical and thermal properties. In this relationship the CIPS process was classified and compared with the literature in more general means for advanced morphology control by differentiating between covalently attached and so-called gradient domain structures. The prepolymers were characterized by ¹H NMR, FT-IR, DSC and TGA. The thermoset morphologies were investigated by TEM and AFM. The fracture toughness (K_Ic) and the elastic modulus (E) were measured by fracture and three point bending experiments. Thermal properties of the resulting films have been tested by DMA.