Grafting of polyaniline onto the radiation crosslinked chitosan

In this paper we report the chemical grafting of polyaniline onto the radiation crosslinked chitosan. Chitosan is crosslinked using 8 MeV electron beam and Co⁶⁰ γ-ray in the presence of CCl₄ as sensitizer. The so-obtained crosslinked chitosan is grafted with polyaniline (PANI) chemically using ammonium peroxy disulphate (APS) as an initiator. Grafted polymer is characterized by dissolution, swelling, UV–vis–NIR spectroscopy, Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), scanning electron microscopy (SEM), thermogravimetric analysis, DC conductivity and nanoindentation studies. From the dissolution studies, grafting of PANI onto the crosslinked chitosan is confirmed. From the weight of films before and after grafting, grafting percentage is calculated. Grafting percentage increases as the monomer concentration increases and decreases with increase in crosslinking. This may be due to the decrease in the penetration of monomer onto the chitosan matrix with increase in crosslinking density. This is verified from SEM (cross-sectional view) of blend. UV–vis–NIR spectrum shows absorption peaks of PANI. Electrical property of grafted polymer is improved after doping with 1 M HCl. The change in volume conductivity is from 10⁻¹¹ to 10⁻⁵ S/cm and surface conductivity from 10⁻¹⁰ to 10⁻² S/cm. From TGA it is observed that grafted polymer and doped polymer are thermally stable.     

Carbon black–polybenzoxazine nanocomposites for high K dielectric applications

This work involves the development of surface functionalized carbon black (FCB) reinforced polybenzoxazine (PBZ) nanocomposites, using a benzoxazine monomer and varying weight percentages of functionalized carbon black (0.5, 1.0, and 1.5 wt%) through ring opening polymerization via thermal cure. Data from the morphological studies indicate that the nanosized FCB particles are homogeneously distributed in the polybenzoxazine matrix. The incorporation of FCB improves the dielectric constant, electrical conductivity, and reduction in resistivity of the resulting FCB–PBZ nanocomposites when compared to neat PBZ. A significant improvement observed in glass transition temperature and thermal stability of resulting FCB–PBZ nanocomposites, when compared to neat PBZ. POLYM. COMPOS., 35:2121–2128, 2014. © 2014 Society of Plastics Engineers     

The role of substrates on the structural,optical, and morphological properties of zno nanotubes prepared by spray pyrolysis

ZnO films were deposited onto glass, ITO coated glass, and sapphire substrate by spray pyrolysis, and subsequently annealed at the same temperature of 400°C for 3 h. The role of substrate on the properties of ZnO films was investigated. The structural and optical properties of the films were investigated by X‐ray diffractometer (XRD) and photoluminescence (PL) spectrophotometer, respectively. The surface morphology of the nanostructured ZnO film was investigated by scanning electron microscopy (SEM) and atomic force microscopy (AFM). Crystallographic properties revealed that the ZnO films deposited on sapphire and ITO substrates exhibit a strong c‐axis orientation of grains with hexagonal wurtzite structure. Extremely high UV emission intensity was determined in the film on ITO. The different luminescence behaviors was discussed, which would be caused by least value of strain in the film. Films grown on different substrates revealed differences in the morphology. ZnO films on ITO and sapphire substrates revealed better morphology than that of the film on glass. AFM images of the films prepared on ITO show uniform distribution of grains with large surface roughness, suitable for application in dye sensitized solar cells. Microsc. Res. Tech. 77:211–215, 2014. © 2013 Wiley Periodicals, Inc.     

Solar cells sensitised by push–pull azo dyes: dependence of photovoltaic performance on electronic structure,geometry and conformation of the sensitizer

Novel Azo dyes possessing varying conjugation lengths and different extents of electron cloud delocalisation were synthesised and characterised and explored as sensitizers for dye-sensitised solar cells (DSSC). The envisaged azo dyes comprising of electron withdrawing and electron-donating moieties which are linked through conjugation bridges of varying lengths facilitated the prevalence of push–pull mechanism in the molecules. Optimisation of the geometry were performed for the synthesised compounds using B3LYP/ 6-31?+?G (d,p) level of density functional theory and their computed optical absorption and band gaps were validated with experimental results. The dyes exhibited molar extinction coefficients in the range of 3.2?×?10⁴ to 4.2?×?10⁴?mol^?1?Lcm^?1. The highest occupied molecular orbital (HOMO) was located between ?5.53 and ?5.03?eV for the various sensitizers synthesised and their lowest unoccupied molecular orbital (LUMO) was located between ?2.86 and ?3.08?eV. HOMO–LUMO gaps were in the range of 2.02–2.67?eV. Fill factor of the cells varied from 28% to 32% and the power conversion efficiencies ranged from 0.4% to 2.7%. This is the first time reporting of a systematic investigation, correlating the influence of nature and position of substituent, extending of conjugation and geometry of sensitizers on the photo physical properties of the sensitizers and the photovoltaic performance of corresponding DSSC.

Highlights

• The article focuses on push–pull azo dyes and were explored as promising candidate sensitizers for low cost dye-sensitised solar cells (DSSC).

• The effect of chemical structure, extend of conjugation and geometry of the sensitizer on the photo physical properties of the sensitizers and the photovoltaic performance of DSSC were analysed.

     

Influence of Coating Parameter and Sintering Atmosphere on the Corrosion Resistance Behavior of Electrophoretically Deposited Composite Coatings

The purpose of this study is to synthesize and characterize nanosized titania (TiO₂), zinc oxide (ZnO), and its composite coating on Ti–6Al–4V to enhance its corrosion protection behavior in Ringer's solution. Nanosized powders of TiO₂ and ZnO was characterized by Fourier transform infrared spectroscopy (FTIR), powder X-ray diffraction (XRD), and scanning electron microscopy - energy dispersive atomic spectroscopy (SEM-EDAX) analysis. As a result of antibacterial activity, both ZnO and TiO₂/ZnO have produce remarkable inhibition zone on Escherichia coli. The antibacterial activity of composites are due to the combined effect of ZnO on TiO₂. The adherence and surface uniformity of TiO₂/ZnO composite film on titanium implant was examined by optical microscopy and Vickers microhardness test. Corrosion resistant behavior of the coating on titanium implant was investigated by tafel polarization and impedance analysis. The composite coatings on Ti–6Al–4V have produced improved corrosion resistance with a pronounced shift in the anodic corrosion potential (E_corr) with a corresponding less corrosion current density (I_corr) compared to monophase coating. Similar results have been obtained for impedance analysis which indicated a reduction in double layer capacitance (C_dl) and with enhancement in charge transfer resistance (R_ct). These observations suggest improved corrosion resistance property of TiO₂/ZnO composite coating on Ti–6Al–4V.     

Biocompatibility assessment of SiO2 –TiO2 composite powder on MG63 osteoblast cell lines for orthopaedic applications

The objective of this study is to evaluate the biocompatibility of composite powder consisting of silica and titania (SiO₂ –TiO₂) for biomedical applications. The advancement of nanoscience and nanotechnology encourages researchers to actively participate in reinvention of existing materials with improved physical, chemical and biological properties. Hence, a composite/hybrid material has given birth of new materials with intriguing properties. In the present investigation, SiO₂ –TiO₂ composite powder was synthesised by sol‐gel method and the prepared nanocomposite was characterised for its phase purity, functional groups, surface topography by powder X‐ray diffraction (XRD), Fourier transform infrared spectroscopy (FT‐IR) and scanning electron microscopy. Furthermore, to understand the adverse effects of composite, biocompatibility test was analysed by cell culture method using MG63 osteoblast cell lines as a basic screening method. From the results, it was observed that typical Si–O–Ti peaks in FT‐IR confirms the formation of composite and the crystallinity of the composite powder was analysed by XRD analysis. Further in vitro biocompatibility and acridine orange results have indicated better biocompatibility at different concentrations on osteoblast cell lines. On the basis of these observations, we envision that the prepared silica–titania nanocomposite is an intriguing biomaterial for better biomedical applications.Inspec keywords: bioceramics, nanocomposites, silicon compounds, titanium compounds, nanofabrication, sol‐gel processing, surface topography, X‐ray diffraction, Fourier transform infrared spectra, scanning electron microscopy, X‐ray chemical analysis, cellular biophysics, nanomedicineOther keywords: MG63 osteoblast cell lines, orthopaedic applications, biomedical applications, nanoscience, nanotechnology, nanotoxicology, physical properties, chemical properties, biological properties, biological applications, biomaterial synthesis, composite‐hybrid materials, intriguing properties, sol‐gel method, surface properties, ceramic nanocomposite, phase purity, functional groups, surface topography, powder X‐ray diffraction, Fourier transform infrared spectroscopy, FT‐IR spectroscopy, scanning electron microscopy, energy dispersive X‐ray analysis, biocompatibility test, cell culture method, screening method, crystallinity, XRD, in vitro biocompatibility, acridine orange, silica‐titania nanocomposite powder, SiO₂ ‐TiO₂      

Electrical properties of ZnSe-CdS alloy films

Thin films of ZnSe _x CdS_1–x (t 0.6 m) over the entire range of x, were deposited on glass substrates at two temperatures, T _s (350 and 470 K) by vacuum evaporation. X-ray diffraction studies showed that all the films were polycrystalline in nature. Films prepared at 470 K were nearly stoichiometric. Grain size increased with substrate temperature, T _s. The electrical conductivity and Hall measurements were carried out by d.c. van der Pauw technique. Hall effect studies/hot probe test showed that all the films were of n-type conductivity. Hall mobility increased with T _s. In addition, mobilities increased with temperature in films of all compositions, indicating the dominance of grain-boundary scattering. Grain-boundary potentials were in range 0.03–0.06 eV.     

Texture evolution in an Al–Cu alloy during equal channel angular pressing: the effect of starting microstructure

In this article, the effect of initial microstructure on the texture evolution in 2014 Al alloy during equal channel angular pressing (ECAP) through route A has been reported. Three heat treatment conditions were chosen to generate the initial microstructures, namely (i) the recrystallization anneal (as-received), (ii) solution treatment at 768 K for 1 h, and (iii) solution treatment (768 K for 1 h) plus aging at 468 K for 5 h. Texture analyses were performed using orientation distribution function (ODF) method. The texture strength after ECAP processing was different for the three samples in the order, solutionised > solutionised plus aged condition > as-received. The prominent texture components were A _E /[`(A)]<sub>E</sub> \bar{A}_{E} and B <sub>E</sub> /[`(B)]_E \bar{B}_{E} in addition to several weaker components for the three materials. The strong texture evolution in solutionised condition has been attributed to higher strain hardening of the matrix due to higher amount of solute. In case of the as-received as well as solutionised plus aged alloy, the weaker texture could be due to the strain scattering from extensive precipitate fragmentation and dissolution during ECAP.     

A novel nanostructured iron oxide-gold bioelectrode for hydrogen peroxide sensing

Fe(3)O(4) nanoparticles covalently linked to a gold electrode have been used for immobilizing catalase (CAT) enzyme to sense the presence of various concentrations of H(2)O(2). These nanoparticles ranging from 20 to 30 nm were synthesized by thermal co-precipitation of ferric and ferrous chlorides. SEM and XRD have been used for morphological and structural characterization of Fe(3)O(4) nanoparticles. CAT enzyme was linked covalently to the surface of iron oxide using carbodiimide in phosphate buffer (pH 7.4) at 4?°C. The enzyme-iron oxide link was confirmed by FT-IR spectroscopy. Sensing studies carried out using cyclic voltammetry showed a linear response of the CAT/nano Fe(3)O(4)/Au bioelectrode towards H(2)O(2) between 1.5 and 13.5 μM with a very sharp response time of 2 s.     

Influence of Fe catalytic doping on the properties of TiO2 nanoparticles synthesized by microwave method

The present work focus on the development of an effective process for undoped and Fe doped TiO₂ powders production by microwave technique. The influence of Fe doping on the structure, phase, vibrational bands and optical properties of TiO₂ were discussed. The X-ray diffraction patterns of nanoparticles revealed a preferentially oriented (101) anatase phase for TiO₂ and transforms to rutile TiO₂ with Fe doping. Fourier transform infrared spectra analysis confirmed the phase transformation from anatase to rutile TiO₂ with Fe doping. The UV–visible spectra showed the increase in absorption band with Fe doping when compared with undoped TiO₂ nano particles, and optical band gap decreased slightly with Fe doping. SEM micrographs revealed spherical shaped grains of TiO₂ with high homogeneity, with a subsequent reduction in the agglomeration of particles with Fe doping suggesting its potential application for better photo catalytic activity.