Dielectric and pyroelectric properties of P(VDF-TrFE) and PCLT–P(VDF-TrFE) 0–3 nanocomposite films

Nanocrystalline calcium and lanthanum modified lead titanate (PCLT) powder prepared by a sol–gel process was incorporated into a polyvinylidene fluoride-trifluoroethylene [P(VDF-TrFE)] copolymer matrix to form PCLT–P(VDF-TrFE) nanocomposite thin films with 0.11 volume fraction of ceramic. The relative permittivity and pyroelectric coefficient of the P(VDF-TrFE) copolymer and nanocomposite films were measured as functions of the poling electric field. After poling under the same conditions, the nanocomposite film was found to have a higher pyroelectric coefficient (by ∼35%) and figures of merit than those of the P(VDF-TrFE) film of a similar thickness.     

Preparation and characterization of pyrolytically deposited (Co–V–O and Cr–V–O) thin films

The metal acetylacetonates of vanadium, cobalt and chromium were prepared from commercial reagents. The corresponding metal acetylacetonates were mixed in desired ratio and deposited on soda lime glass substrate by metal organic chemical vapor deposition technique. Mixed oxides thin films with atomic composition Co_0.31V_1.37O₅ and Cr_0.5V₂O₅ were obtained. A combination of Rutherford backscattering spectroscopy and energy-dispersive X-ray fluorescence was used for the transition element identification and atomic compositional study of the thin films. The thickness of the Co–V–O and Cr–V–O thin films was 166 and 127 nm, respectively. The optical spectra of the films were obtained using a Pye Unicam SP8-400 spectrophotometer in the ultraviolet/visible region. The result of the spectral analyses gave the optical bandgap energy of the materials. The temperature dependence of the electrical resistivity measured using the Van der Pauw method indicated that the materials are semiconducting. Their activation energy was obtained from plots of the natural logarithm of conductivity vs. the reciprocal of temperature. The sign of the thermopower shows that both materials are p-type semiconductors.     

Electrical and humidity sensing properties of lead(II) tungstate–tungsten(VI) oxide and zinc(II) tungstate–tungsten(VI) oxide composites

Lead(II) tungstate and zinc(II) tungstate were prepared by a solution route and sintered at 973 K in the form of cylindrical discs. Experimental results on PbWO₄ (PW) and WO₃ (WO) composites for humidity sensing are described. Sintered polycrystalline discs of PbWO₄ (PWWO-10), WO₃ (PWWO-01), ZnWO₄ (ZWWO-10) and composites of PW or ZW and WO in the mole ratios 8:2, 6:4, 4:6, 2:8 designated as PWWO and ZWWO-82, 64, 46 and 28, respectively and doped with 2 mol% of Li⁺ were studied. The composites were subjected to dc conductance measurements over the temperature range 373–673 K in air atmosphere from which activation energies were determined. The activation energy values for dc conductance were found to be in the range of 1.09–1.30 eV. The composites were identified by powder XRD data. The scanning electron microscopy (SEM) studies were carried out to study the surface and pores structure of the sensor materials. The composites were subjected to dc resistance measurements as a function of relative humidity in the range of 5–98% RH, achieved by different water vapor buffers thermostated at room temperature. The sensitivity factor (S_f=R_5%/R_98%) measured at 298 K revealed that PWWO-28 and ZWWO-46 composites have the highest humidity sensitivity factor of 17 615±3000 and 2666±550, respectively. The response and recovery time for these humidity sensing composites were good.     

Investigation of effects of Argenine–Glycine–Aspartate (RGD) and nano-scale titanium coatings on cell spreading and adhesion

This paper examines the effects of physical and chemical surface modifications on the biocompatibility of silicon surfaces that are relevant to implantable silicon Bio-micro-electro-mechanical systems (BioMEMS). Two types of surface modifications were explored. The first involved the deposition of nano-scale biocompatible layers of pure titanium on silicon, while the second explored the covalent attachment of the binding peptide Argenine–Glycine–Aspartic acid (RGD) for improved cell adhesion. Improvements in biocompatibility were assessed through examination of cell areas after culture, as well as the measurements of adhesion strengths, as determined by shear assay techniques. The titanium nanolayers and the RGD coating resulted in improvements in biocompatibility. Increased cell spreading areas and improved adhesion strength were obtained from short and long-term studies of Human Osteosarcoma (HOS) cells cultured on the coated surfaces. RGD functionalization resulted in the greatest improvement in cell spreading area and adhesion strength for short culture times. The effects of the titanium, while less than those of RGD for short culture times, appeared to be greater after 48 h of culture.     

Properties and microstructure of WC–TiC–Co and WC–TiC–MO2C–Co(Ni) cemented carbides

Abstract

The present study is an attempt to observe the changes in microstructure and properties of modified WC–10Co cemented carbides from the viewpoint of the distinctive role played by modified binder phase. Introduction of TiC into WC–10Co cemented carbide results in microstructural non-uniformity, i.e. a wide range of grain size distribution, which in turn gives rise to a drastic drop in values of transverse rupture strength and toughness. The modification of binder and carbide phases by incorporating, respectively, nickel and M02C improves the microstructural uniformity, which ensures better mechanical properties. The present findings have been interpreted in terms of various quantitative microstructural parameters, with particular attention being given to the wettability factor.

MST/1363     

Synthesis and phases evolution of Si–C–Ti from polycarbosilane (PCS) and metal Ti

Si–C–Ti ceramics were synthesized by reactive pyrolysis of polycarbosilane (PCS) precursor filled with metal Ti powder. Pyrolysis of mixture with atomic ratio of Ti:Si through 3:1–3:2 was carried out in argon atmosphere at given temperature up to 1500 °C. The metal–precursor reactions, and phase evolution were studied using X-ray diffraction and scanning electron microscopy with EDX. The Ti₃SiC₂ phase was obtained firstly from reaction of PCS and Ti. Ti₃SiC₂ formation starts at 1300 °C and its amount increases significantly in a narrow temperature range between 1400 °C and 1500 °C. In addition, addition of CaF₂ can promote the formation of Ti₃SiC₂ phase.     

Preparation and characterization of hydroxyl (–OH) functionalized multi-walled carbon nanotube (MWCNT)–Dowtherm A nanofluids

In the present work, the thermal conductivity and viscosity of hydroxyl (–OH) functionalized multi-walled carbon nanotubes (MWCNTs)–Dowtherm A (eutectic mixture of biphenyl (C₁₂H₁₀) and diphenyl oxide (C₁₂H₁₀O)) nanofluids are discussed. As-received hydroxyl (–OH) functionalized MWCNTs are characterized using x-ray diffraction (XRD), FT-Raman spectroscopy, Fourier transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), and thermogravimetry, differential thermogravimetry, and differential scanning calorimetry (TGA-DTG/DSC) analysis. Hydroxyl (–OH) functionalized MWCNT–Dowtherm A nanofluids are prepared in different concentrations (0.001–0.005?g) of MWCNT and characterized at various temperatures (303–323?K). The thermal conductivity of hydroxyl (–OH) functionalized MWCNT–Dowtherm A nanofluids increases with the concentration of carbon nanotubes as well as with temperature. The possible mechanism for the enhancement observed may be ascribed to the percolation of heat through the nanotubes to form a tri-dimensional network. Also, as the temperature increases, the viscosity of the nanofluid decreases, which results in an increase in Brownian motion of nanoparticles, this sets convection-like effects resulting in enhanced thermal conductivity.     

Influence of cerium oxide (CeO2) nanoparticles on the microstructure and hardness of tin–silver–copper (Sn–Ag–Cu) solders on silver (Ag) surface-finished copper (Cu) substrates

Nano-sized, non-reacting, non-coarsening CeO₂ particles with a density close to that of solder alloy were incorporated into Sn–3.0 wt%Ag–0.5 wt%Cu solder paste. The interfacial microstructure and hardness of Ag surface-finished Cu substrates were investigated, as a function of reaction time, at various temperatures. After the initial reaction, an island-shaped Cu₆Sn₅ intermetallic compound (IMC) layer was clearly observed at the interfaces of the Sn–Ag–Cu based solders/immersion Ag plated Cu substrates. However, after a prolonged reaction, a very thin, firmly adhering Cu₃Sn IMC layer was observed between the Cu₆Sn₅ IMC layer and the substrates. Rod-like Ag₃Sn IMC particles were also clearly observed at the interfaces. At the interfaces of the Sn–Ag–Cu based solder-Ag/Ni metallized Cu substrates, a (Cu, Ni)–Sn IMC layer was found. Rod-like Ag₃Sn and needle-shaped Cu₆Sn₅ IMC particles were also observed on the top surface of the (Cu, Ni)–Sn IMC layer. As the temperature and reaction time increased, so did the thickness of the IMC layers. In the solder ball region of both systems, a fine microstructure of Ag₃Sn, Cu₆Sn₅ IMC particles appeared in the β-Sn matrix. However, the growth behavior of the IMC layers of composite solder doped with CeO₂ nanoparticles was inhibited, due to an accumulation of surface-active CeO₂ nanoparticles at the grain boundary or in the IMC layers. In addition, the composite solder joint doped with CeO₂ nanoparticles had a higher hardness value than the plain Sn–Ag–Cu solder joints, due to a well-controlled fine microstructure and uniformly distributed CeO₂ nanoparticles. After 5 min of reaction on immersion Ag-plated Cu substrates at 250 °C, the micro-hardness values of the plain Sn–Ag–Cu solder joint and the composite solder joints containing 1 wt% of CeO₂ nanoparticles were approximately 16.6 and 18.6 Hv, respectively. However after 30 min of reaction, the hardness values were approximately 14.4 and 16.6 Hv, while the micro-hardness values of the plain Sn–Ag–Cu solder joints and the composite solder joints on Ag/Ni metallized Cu substrates after 5 min of reaction at 250 °C were approximately 15.9 and 17.4 Hv, respectively. After 30 min of reaction, values of approximately 14.4 and 15.5 Hv were recorded.     

Structure and Properties of Nanostructured Vacuum-Deposited Foils of Invar Fe–(35–38 wt%)Ni Alloys

The process of electron beam vacuum deposition of the Fe–(35–38 wt%)Ni alloys at substrate temperatures Ts from 300 to700 °C were used to produce vacuum-deposited foils with the FCC structure, differing by the size of characteristic microstructural elements(grains and subgrains). It was shown that refinement of foil microstructural elements to nanoscale is accompanied by their microhardness increase up to 4–5 GPa. The change of the thermal expansion coefficient(TEC) of the nanostructured(NS) foil of the Fe–35.1Ni alloy within the temperature range from-50 to 150 °C has some deviation from that observed for cast Invar alloy of the same composition. It has been found that the main factors affecting the peculiarities of thermal expansion of the NS foil can be related to the presence of small fraction of BCCphase in them, high level of crystalline lattice microstrains and inhomogeneous magnetic order in FCCphase. It was shown that as a result of additional thermal treatment of NS foils their invar properties become similar to that observed for cast Invar alloy but mechanical properties remain on the same level.     

Interfacial microstructure and hardness of nickel (Ni) nanoparticle-doped tin–silver–copper (Sn–Ag–Cu) solders on immersion silver (Ag)-plated copper (Cu) substrates

Sn–Ag–Cu composite solder has been prepared by adding Ni nanoparticles. Interfacial reactions, the morphology of the intermetallic compounds (IMC) that were formed, the hardness between the solder joints and the plain Cu/immersion Ag-plated Cu pads depending on the number of the reflow cycles and the aging time have all been investigated. A scallop-shaped Cu₆Sn₅ IMC layer that adhered to the substrate surface was formed at the interfaces of the plain Sn–Ag–Cu solder joints during the early reflow cycles. A very thin Cu₃Sn IMC layer was found between the Cu₆Sn₅ IMC layer and the substrates after a lengthy reflow cycle and solid-state aging process. However, after adding Ni nanoparticles, a scallop-shaped (Cu, Ni)–Sn IMC layer was clearly observed at both of the substrate surfaces, without any Cu₃Sn IMC layer formation. Needle-shaped Ag₃Sn and sphere-shaped Cu₆Sn₅ IMC particles were clearly observed in the β-Sn matrix in the solder-ball region of the plain Sn–Ag–Cu solder joints. Additional fine (Cu, Ni)-Sn IMC particles were found to be homogeneously distributed in the β-Sn matrix of the solder joints containing the Ni nanoparticles. The Sn–Ag–Cu–0.5Ni composite solder joints consistently displayed higher hardness values than the plain Sn–Ag–Cu solder joints for any specific number of reflow cycles–on both substrates–due to their well-controlled, fine network-type microstructures and the homogeneous distribution of fine (Cu, Ni)–Sn IMC particles, which acted as second-phase strengthening mechanisms. The hardness values of Sn–Ag–Cu and Sn–Ag–Cu–0.5Ni on the Cu substrates after one reflow cycle were about 15.1 and 16.6 Hv, respectively–and about 12.2 and 14.4 Hv after sixteen reflow cycles, respectively. However, the hardness values of the plain Sn–Ag–Cu solder joint and solder joint containing 0.5 wt% Ni nanoparticles after one reflow cycle on the immersion Ag plated Cu substrates were about 17.7 and 18.7 Hv, respectively, and about 13.2 and 15.3 Hv after sixteen reflow cycles, respectively.     

Strength and mechanical behavior of soil–cement–lime–rice husk ash (soil–CLR) mixture

This study presents results of geotechnical investigations on treated silty sand soil with cement, lime and rice husk ash (CLR) and cement-lime (CL) admixture. Consolidated undrained triaxial test and unconfined compressive test were performed to estimate the potential of CLR and CL. The study investigates the influence of the amount of CLR%, main effective stress and curing days on soil strength, deformation, post peak behavior and brittleness. The percentages of the additives of CLR and CL varied from 2.5 to 12.5 % by dry weight of the soil with dry densities of 14.5 kN/m³ and the curing times of 3, 7, 28 and 60 days were examined. From the results, the stress–strain response is strongly influenced by the CLR contents and effective confining pressure. Strength and post peak strength of the CLR–soil are greatly improved by an increase in binder content. An increase of the effective cohesion c′ (kPa) and effective friction Φ′ (degree) is observed with increasing the CLR content, consistently. Brittle behavior observed at lower confining pressures and high CLR content. For both CLR and CL additives, linear trend was observed for variation of the q _u (kPa) with respect to the additives percentages. RHA was also found to be effective in increasing the shear strength of CLR–soil mixture.     

Evolution of crystallization and its effects on properties during pyrolysis of Si–Al–C–(O) precursor fibers

The high-temperature resistant Si–Al–C–(O) fibers were prepared through polymer-derived method using continuous polyaluminocarbosilane (PACS) fibers. Evolutions of the crystallization during the pyrolysis of the Si–Al–C–(O) precursor fibers were investigated by a series analysis. The structure of the fibers transforms from organic state to inorganic state and the crystalline phases appear during the pyrolysis. The β-SiC crystallite size increases when the temperature is higher than 1,300 °C. At the same time, the α-SiC appears. At 1,600 and 1,800 °C, the grain size of β-SiC of the fibers is 15.4 and 22.1 nm, respectively. The growth of β-SiC and the appearing of α-SiC have a great influence on the properties of the fibers. The change of the tensile strength of the pyrolysis products is divided into three stages with the growth of the crystal. The tensile strength of the Si-Al-C fibers is higher than 1.9 GPa.     

Tissue engineering scaffolds of mesoporous magnesium silicate and poly(ε-caprolactone)–poly(ethylene glycol)–poly(ε-caprolactone) composite

Mesoporous magnesium silicate (m-MS) and poly(ε-caprolactone)–poly(ethylene glycol)–poly(ε-caprolactone) (PCL–PEG–PCL) composite scaffolds were fabricated by solvent-casting and particulate leaching method. The results suggested that the incorporation of m-MS into PCL–PEG–PCL could significantly improve the water adsorption of the m-MS/PCL–PEG–PCL composite (m-MPC) scaffolds. The in vitro degradation behavior of m-MPC scaffolds were determined by testing weight loss of the scaffolds after soaking into phosphate buffered saline (PBS), and the result showed that the degradation of m-MPC scaffolds was obviously enhanced by addition of m-MS into PCL–PEG–PCL after soaking for 10 weeks. Proliferation of MG63 cells on m-MPC was significantly higher than MPC scaffolds at 4 and 7 days. ALP activity on the m-MPC was obviously higher than MPC scaffolds at 7 days, revealing that m-MPC could promote cell differentiation. Histological evaluation showed that the introduction of m-MS into PCL–PEG–PCL enhanced the efficiency of new bone formation when the m-MPC scaffolds implanted into bone defect of rabbits. The results suggested that the inorganic/organic composite of m-MS and PCL–PEG–PCL scaffolds exhibited good biocompatibility, degradability and osteogenesis.     

Structure and dielectric properties of a new series of pyrochlores in the Ca–Sm–Ti–M–O (M = Nb and Ta) system

The present work investigates the dielectric properties of pyrochlore type oxides, Ca–Sm–Ti–M–O (M = Nb and Ta) in the low frequency region (100 Hz–1 MHz) over the temperature range 30–100 °C. The 1 MHz dielectric constants (K) of these oxides are in the range 23–108 and show low variation with frequency (1 kHz–1 MHz). The temperature coefficient of dielectric constant (TCK) over the temperature range varies from positive to negative values in the range 48 to −107 ppm/°C. Rietveld analysis of the X-ray diffraction data establishes a cubic pyrochlore-type phase in the space group Fd3 m (no. 227).The grain morphology observation by scanning electron microscope shows well sintered grains.     

Structural and optical properties of inorganic–organic hybrid material of acetanilide tetrachloromercurate(II)

The crystal growth of acetanilide tetrachloromercurate(II), an inorganic–organic hybrid derivative has been achieved by solution growth through slow cooling method. The X-ray diffraction structural analysis of the hybrid material results that the compound exist in orthorhombic space group P2₁2₁2₁ with lattice parameters; a?=?13.111(2) ?, b?=?11.311(2) ?, c?=?8.355(6) ?, α?=?β?=?γ?=?90° and unit cell volume?=?1436.24 ?³. The fourier transform infrared spectroscopy profile shows that the C–C and C–N stretching modes of acetanilide ring and the observed spectra falls in mid-infrared range υ(526–2850) cm^?1. The field emission scanning electron microscope image confirms that the hybrid material has a prismatic shape with an average granular size of ~25 nm. The energy dispersive X-ray spectroscopy analyzes the elemental proportions of the hybrid materials. Transmission electron microscopy image shows the narrow distribution of nano-spatial agglomeration of secondary interactions in inorganic–organic particles. The optical band gap (Eg?=?3.75 eV) as calculated by linear fit profile of Tauc plot for allowed transition predicts that the hybrid material has potential applications in solar cells, electronic and opto-electronic devices.     

Effects of minor Zr and Sr on as-cast microstructure and mechanical properties of Mg–3Ce–1.2Mn–1Zn (wt%) magnesium alloy

The effects of minor Zr and Sr on the as-cast microstructure and mechanical properties of the Mg–3Ce–1.2Mn–1Zn (wt%) alloy were investigated. The results indicate that adding minor Zr and/or Sr to the Mg–3Ce–1.2Mn–1Zn alloy does not cause an obvious change in the morphology and distribution of the Mg₁₂Ce phase. However, the grains of the Zr- and/or Sr-containing alloys are effectively refined. Among the Zr- and/or Sr-containing alloys, the grains of the alloy with the addition of 0.5 wt%Zr + 0.1 wt%Sr are the finest. Furthermore, adding minor Zr and/or Sr to the Mg–3Ce–1.2Mn–1Zn alloy can improve the tensile properties. Among the Zr- and/or Sr-containing alloys, the alloy with the addition of 0.5 wt%Zr + 0.1 wt%Sr obtains the optimum tensile properties. In addition, adding minor Zr and/or Sr to the Mg–3Ce–1.2Mn–1Zn alloy also can improve the creep properties, and the creep properties of the three alloys with the additions of 0.5 wt%Zr + 0.1 wt%Sr, 0.5 wt%Zr, and 0.1 wt%Sr are similar.     

Publication-rate and size of two prolific research groups in departments of inorganic chemistry at Dacca University (1944–1965) and Zoology at Karachi University (1966–84)

There has been considerable interest in studying how the research output of a group of N researchers depends on the group-size, N. Several workers have studied this, but with conflicting conclusions, ranging from finding constant per-capita output to per-capita output varying linearly as N, and even exponentially with N. The present communication states afresh the author's earlier theory of productive interactions and gives analyses of the outputs of two prolific research groups: one from Dhaka University, Bangladesh, and one from Karachi University, Pakistan, each over nearly two decades. The data, obtained from published bibliographies, are sub-divided into small successive ranges of lab. group size, 1–2, 3–4, 5–6, etc., and analyzed by calculating the relevant publication-rate per person (R) for each range. Plots of the data from each group show evidence of an initial approx, linear rise of per-capita publication rate, R, up to about N=5, followed by a maximum at group-size of 6 to 8 persons. This group size would correspond to the optimum efficiency, as a balance between the benefits of increasing interaction ( N²) and Parkinsonian loss of efficiency. This is in agreement with the first peak in the author's earlier analysis (of recent U.K. and U.S.A. data) published five years ago inScientometrics, as well as his previous work published elsewhere. Possible reasons for the failure of statistical criteria to show up this phenomenon of increasing per-capita output are indicated and further indepth studies on two University research groups are planned.Dedicated to the memory of Michael J. Moravcsik     

Transformation behavior and shape memory characteristics of thermo-mechanically treated Ti–(45−x)Ni–5Cu–xV (at%) alloys

Transformation behavior, shape memory characteristics and superelasticity of thermo-mechanically treated Ti–(45?x)Ni–5Cu–xV (at%) (x = 0.5–2.0) alloys were investigated by means of differential scanning calorimetry, transmission electron microscopy, X-ray diffractions, thermal cycling tests under constant load and tensile tests. The B2–B19′ transformation occurred when V content was 0.5 at%, above which the B2–B19–B19′ transformation occurred. The B2–B19 transformation was not separated clearly from the B19–B19′ transformation. Thermo-mechanically treated Ti–(45?x)Ni–5Cu–xV alloys showed perfect shape memory effect and transformation hysteresis(ΔT) of Ti–43.5Ni–5.0Cu–1.5V and Ti–43.0Ni–5.0Cu–2.0V alloys was about 9 K which was much smaller than that of a Ti–44.5Ni–5.0Cu–0.5V alloy(23.3 K). More than 90% of superelastic recovery ratio was observed in all specimens and transformation hysteresis (Δσ) of a Ti–44.5Ni–5.0Cu–0.5V alloy was about 70 MPa, which was much larger than that of a Ti–43.0Ni–5.0Cu–2.0V alloy (35 MPa).     

Layer-by-layer assembly of poly(p-xylyleneviologen)–DNA multilayers and their electrochemical properties

Multilayers of poly(p-xylyleneviologen) (PXV) and calf thymus DNA were constructed on the gold surface by layer-by-layer (LBL) method. The assembly process was examined by quartz crystal microbalance (QCM) measurements. According to the frequency change, the average mass increase was estimated to be about 97 and 110 ng/cm² for each assembly of PXV and DNA layer, respectively. Cyclic voltammograms of the multilayer modified gold electrodes showed a couple of redox peaks, the potentials of which were closely dependent on the layer numbers and nature of the outmost layer. The alternatively assembled DNA layers could hinder formation of π-complex dimer of viologen groups due to the strong interlayer electrostatic interaction. The charge transfer process was discussed by the chronocoulometry method. The assembled PXV–DNA multilayers showed high long-term stability at ambient conditions and in electrolyte solution.     

Microstructure and texture assessment of Al–Mn–Fe–Si (3003) aluminum alloy produced by continuous and semicontinuous casting processes

Aluminum sheets are currently produced by the direct-chill process (DC). The need for low-cost aluminum sheets is a challenge for the development of new materials produced by the twin roll caster (TRC) process. It is expected that sheets produced from these different casting procedures will differ in their microstructure. These differences in microstructure and in the crystallographic texture have great impact on sheet mechanical properties and formability. The present study investigated microstructure and evaluated texture of two strips of Al–Mn-Fe–Si (3003) aluminum alloy produced by TRC and by hot-rolling processes. It was possible to notice that the microstructure, morphology, and grain size of the TRC sample were more homogenous than those found in hot-rolled samples. Both strips, obtained by the two processes, showed strong texture gradient across the thickness.