Sonochemical synthesis of crystalline nanoporous zinc oxide spheres and their application in dye-sensitized solar cells

A composite material made of zinc oxide and polyvinyl alcohol was prepared by a sonochemical method. Annealing of the composite under air removed the polymer, leaving porous spheres of ZnO. This change was accompanied by a change of the surface area from 2 m²/g to 34 m²/g. The porous ZnO particles were used as the electrode material for dye-sensitized solar cells (DSSCs). It was tested by forming a film of the doped porous ZnO on a conductive glass support. The performance of the solar cell is reported.     

Immobilization of cholesterol oxidase and potassium ferricyanide on dodecylbenzene sulfonate ion‐doped polypyrrole film

Dodecylbenzene sulfonate (DBS)‐doped polypyrrole (PPY) conducting polymer films were electrochemically deposited onto the indium‐tin‐oxide (ITO)‐coated glass plates in aqueous medium. The enzyme cholesterol oxidase (ChOx) was immobilized on these DBS–PPY films by a physical adsorption technique. These ChOx‐immobilized DBS–PPY films were characterized by ultraviolet–visible and Fourier transform infrared spectroscopy. The enzyme activity studies indicate that ～40% of ChOx leaches out from the ChOx/DBS–PPY film. The ChOx activity in the ChOx/DBS–PPY film was assayed as a function of cholesterol concentration. The results of amperometric measurements conducted on ChOx/DBS–PPY/ITO film show linearity over the range 2–8 mM of cholesterol solution. The ChOx/DBS–PPY/ITO electrodes exhibit a response time of 30 s and are stable for ～3 months at 4 °C. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 82: 3486–3491, 2001     

Novel method for preparation of carboxylated nitrile rubber–natural rubber blends using bis(diisopropyl)thiophosphoryl polysulfides

Bis(diisopropyl)thiophosphoryl trisulfide (DIPTRI) and bis(diisopropyl)thiophosphoryl tetrasulfide (DIPTET) are successfully used as a novel coupling agent and accelerator, respectively, to covulcanize an elastomer blend comprising polar carboxylated nitrile rubber (XNBR) and nonpolar natural rubber (NR). These compounds are capable of forming a chemical link between these dissimilar rubbers to produce a technologically compatible blend as judged by a swelling experiment. The blend vulcanizates thus produced exhibit enhanced physical properties that can further be improved by adopting the two‐stage vulcanization technique and also by judicious selection of the NR:XNBR ratio. The blend morphology assessed by scanning electron microcroscopy micrographs accounts for significant improvement in the physical properties of the blend vulcanizates, particularly in two‐stage vulcanization. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 80: 1725–1736, 2001     

Preparation and characterization of siliconized epoxy/bismaleimide (N,N′‐bismaleimido‐4,4′‐diphenyl methane) intercrosslinked matrices for engineering applications

Novel hybrid intercrosslinked networks of hydroxyl‐terminated polydimethylsiloxane‐modified epoxy and bismaleimide matrix systems have been developed. Epoxy systems modified with 5, 10, and 15 wt % of hydroxyl‐terminated polydimethylsiloxane (HTPDMS) were developed by using epoxy resin and hydroxyl‐terminated polydimethylsiloxane with γ‐aminopropyltriethoxysilane (γ‐APS) as compatibilizer and dibutyltindilaurate as catalyst. The reaction between hydroxyl‐terminated polydimethylsiloxane and epoxy resin was confirmed by IR spectral studies. The siliconized epoxy systems were further modified with 5, 10, and 15 wt % of bismaleimide (BMI). The matrices, in the form of castings, were characterized for their mechanical properties. Differential scanning calorimetry and thermogravimetric analysis of the matrix samples were also performed to determine the glass‐transition temperature and thermal‐degradation temperature of the systems. Data obtained from mechanical studies and thermal characterization indicate that the introduction of siloxane into epoxy improves the toughness and thermal stability of epoxy resin with reduction in strength and modulus values. Similarly the incorporation of bismaleimde into epoxy resin improved both tensile strength and thermal behavior of epoxy resin. However, the introduction of siloxane and bismaleimide into epoxy enhances both the mechanical and thermal properties according to their percentage content. Among the siliconized epoxy/bismaleimide intercrosslinked matrices, the epoxy matrix having 5% siloxane and 15% bismaleimide exhibited better mechanical and thermal properties than did matrices having other combinations. The resulting siliconized (5%) epoxy bismaleimide (15%) matrix can be used in the place of unmodified epoxy for the fabrication of aerospace and engineering composite components for better performance. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 81: 38–46, 2001     

The effect of hexamethylene diisocyanate modified ALCELL lignin as a coupling agent on the flexural properties of oil palm empty fruit bunch – polypropylene composites

ALCELL lignin has been employed as a coupling agent in oil palm empty fruit bunch (EFB)–polypropylene (PP) composites. The lignin has been chemically modified with hexamethylene diisocyanate (HMDI). Evidence for the reaction between HMDI and lignin has been observed by using Fourier transform infrared (FTIR) analysis. The effect of lignin as a coupling agent on the flexural properties has been studied. The results show that the HMDI‐modified lignin is able to impart greater compatibility between EFB and PP. This is reflected in the greater flexural strength shown by the composites with HMDI‐modified lignin than those with the unmodified lignin. Scanning electron microscopy studies show that HMDI‐modification of lignin results in a better blending and compatibility between lignin and PP matrix. The glass transition temperature of lignin increases as the level of HMDI modification is increased. © 2001 Society of Chemical Industry     

Ceria (La3+, Sr2+)/Carbonates Nanocomposite Electrolytes with High Electrical Conductivity for Low‐Temperature SOFCs

A series of ceria‐based nanocomposites consisting of lanthanum and strontium codoped ceria with composition Ce_0.89La_0.07Sr_0.04O_1.925 (CL7S4) and eutectic mixture of carbonates Li₂CO₃‐Na₂CO₃ (LNCO) have been prepared by mixing nanosize powders of CL7S4 and LNCO. Samples have been characterized using differential thermal analysis, X‐ray diffraction, scanning electron microscopy combined with energy‐dispersive spectroscopy, thermal expansion, and impedance spectroscopy. A sharp increase in ionic conductivity is observed in all the composite specimens corresponding to superionic transition. Sample containing 35 wt% of carbonate shows the maximum conductivity (2.56 × 10^?1 S/cm at 500°C) with activation energy of conduction, E_a 0.23 eV.     

Phase Evolution,Magnetic, Optical,and Dielectric Properties of Zr‐Substituted Bi0.9Gd0.1FeO3 Multiferroics

Polycrystalline BiFeO₃ (BFO) and Bi_0.90Gd_0.10Fe_1?xZr_xO₃ (x = 0.0–0.10; BGFZ_x) ceramics were synthesized by solid‐state reaction method. Rietveld analysis of X‐ray diffraction patterns showed that BFO and BGFZ_x = 0.0 samples are stabilized in rhombohedral structure (space group R3c), whereas a small fraction of orthorhombic phase (space group Pn2₁a) is observed for BGFZ_{x = 0.03–0.10} samples. Suppression and disappearance of some Raman modes indicated a structural phase transition with addition of Zr dopant at Fe site. Magnetic measurements exhibited weak ferromagnetic behavior of BGFZ_x samples with increasing Zr⁺⁴ concentrations. The insertion of Gd⁺³ ions at Bi⁺³ sites and nonmagnetic Zr⁺⁴ ions at Fe⁺³ sites in Fe–O–Fe network suppressed the spin cycloid structure of BFO which in turn enhanced the magnetization of these ceramics. Electron spin resonance spectra revealed the breaking of spin cycloid of BFO due to the development of free spins with addition of Zr⁺⁴ dopants at Fe sites. UV–Visible diffuse reflectance spectra showed one d–d crystal field transition and two charge‐transfer (C–T) transitions along with a sharp absorption of light in visible region for all samples. Almost frequency‐independent dielectric constant and dielectric loss along with very low values of dielectric loss indicated greatly improved dielectric properties for BGFZ_{x = 0.03–0.10} samples.     

Carbon Doping in Boron Suboxide: Structure,Energetics, and Elastic Properties

The structural, electronic, and elastic properties of pristine and carbon‐doped boron suboxide (B₆O) are calculated using density functional theory. The results indicate that it is energetically preferable for a single carbon atom to substitute into an oxygen site rather than a boron site. The lattice parameters and cell volume increase to relieve the residual stress created by the carbon substitution. The interstitial position is not favorable for a single atom substitution. However, if two carbon atoms substitute for two neighboring oxygen atoms, then it becomes energetically favorable to dope an interstitial oxygen, boron, or carbon atom along the C–C chain. If the interstitial dopant is either boron or carbon, a local B₄C‐like structure with either a C–B–C or C–C–C chain is created within the boron suboxide unit cell. The resulting structure shows improvements in the bulk modulus at the expense of the shear and Young's moduli. The moduli further improve if an additional carbon is substituted within a polar or equatorial site of the neighboring B₁₂ icosahedron. Based on these calculations, we conclude that carbon doping can either harden or soften B₆O depending on the manner in which the substitutions are populated. Furthermore, as B₆O samples are often oxygen deficient, C doping can occupy such sites and improve the elastic properties.