Effect of different solvents on the key structural,optical and electronic properties of sol–gel dip coated AZO nanostructured thin films for optoelectronic applications

Transparent conducting aluminum (i.e. 2 at.%) doped zinc oxide (AZO) thin films were prepared on glass substrates by sol–gel dip coating technique using different solvents. This inexpensive dip coating method involves dipping of substrate consecutively in zinc solution and tube furnace for required cycles. Prepared films were investigated by XRD, SEM, PL, Raman spectroscopy optical and electrical studies. From the XRD studies, it confirmed the incorporation of aluminum in ZnO lattice. The prepared samples are polycrystalline nature, and these films reveal hexagonal wurtzite arrangement with (002) direction. The structural parameters such as crystallite size, dislocation density, micro strain, texture coefficient and lattice constant were investigated. SEM study showed well defined smooth and uniformed ganglia shaped grains are regularly distributed on to the entire glass substrate without any pinholes and cracks, and the average grain size is 75 nm. From the optical studies, the observed highest transmittance is 93% in the visible range and the band gap (E_g) is 3.26 eV. Room temperature PL spectra exhibited strong UV emission peak located at 386 nm for all the films. The electrical properties of the AZO thin films were studied by Hall-Effect measurements and found as n-type conductivity with high carrier concentrations (n), 2.76?×?10¹⁹ cm^??3 and low resistivity (ρ), 7.56?×?10^??3 Ω cm for the film deposed using methanol as solvent.     

Self-assembled nanocomposite of organic-inorganic hybrid: 2,4-dichlorophenoxyacetate in Zn-Al hydrotalcite-like layers

Hydrotalcite-like inorganic layers of Zn-Al, a host containing an organic moiety, 2,4-dichlorophenoxy-acetate, as a guest, was prepared by the spontaneous self-assembly method from an aqueous solution for the formation of a new layered organic-inorganic hybrid nanocomposite material. In this synthesis, the host- and guest-forming species were simultaneously included in the mother liquor, aged, and separated. Various Zn/Al ratios (R = 2, 3, and 4), concentrations of 2,4-dichlorophenoxyacetic acid (0.03-0.1 M), and pH (7 and 10) were studied to optimize the formation of the layered nancomposite. It was found that the optimum conditions for the formation of the nanocomposite were R = 4, pH 7, and concentration of 2,4-dichlorophenoxyacetic acid = 0.08 M. X-ray diffraction shows that this sample affords a nanolayered structure with a basal spacing of 24.6 A.     

Crystalline rice husk silica reinforced AA7075 aluminium chips by cold compaction method

Aluminium matrix composite is highly demanded in various industries due to its low density and good mechanical properties as most commonly studied for metal matrix composite. The properties of the composite be improved with the addition of reinforcement significantly such as silicon carbide, aluminium oxide, and boron carbide that can be mixed easily to metal matrix composite. The study of crystalline rice husk silica reinforced AA7075 aluminium chips on mechanical properties were investigated. The rice husk ash was burned at 1200 °C and it was characterized in the crystalline phase by conducting x-ray diffraction test. The mechanical properties of aluminium matrix composite were obtained by microhardness and compression tests. Results of mechanical properties for the addition of rice husk silica up to 7.5 wt.% composition of crystalline rice husk silica showed increase value of microhardness and compression strength which are the highest value of 75.94 HV 0.1 and 443 MPa, respectively compared to another aluminium matrix composite. Hence, based on investigation to crystalline rice husk silica reinforced aluminium, it has good potential to improve the mechanical properties of aluminium matrix composite which were dependent to the composition of crystalline rice husk silica reinforcement in aluminium matrix composite.     

Enhanced stability and permeation potential of nanoemulsion containing sefsol-218 oil for topical delivery of amphotericin B

Aim: To characterize the enhanced stability and permeation potential of amphotericin B nanoemulsion comprising sefsol-218 oil at varying pH and temperature of aqueous continuous phase.

Methodology: Several batches of amphotericin B loaded nanoemulsion were prepared and evaluated for their physical and chemical stability at different pH and temperature. Also, a comparative study of ex vivo drug permeation across the albino rat skin was investigated with commercial Fungisome® and drug solution at 37?°C for 24?h. The extent of drug penetrated through the rat skin was thereby evaluated using the confocal laser scanning microscopy (CLSM).

Results and conclusions: The optimized nanoemulsion demonstrated the highest flux rate 17.85?±?0.5?µg/cm²/h than drug solution (5.37?±?0.01?µg/cm²/h) and Fungisome® (7.97?±?0.01?µg/cm²/h). Ex vivo drug penetration mechanism from the developed formulations at pH 6.8 and pH 7.4 of aqueous phase pH using the CLSM revealed enhanced penetration. Ex vivo drug penetration studies of developed formulation comprising of CLSM revealed enhanced penetration in aqueous phase at pH 6.8 and 7.4. The aggregation behavior of nanoemulsion at both the pH was found to be minimum and non-nephrotoxic. The stability of amphotericin B was obtained in terms of pH, optical density, globular size, polydispersity index and zeta potential value at different temperature for 90 days. The slowest drug degradation was observed in aqueous phase at pH 7.4 with shelf life 20.03-folds higher when stored at 4?°C (3.8 years) and 5-fold higher at 25?°C (0.951 years) than at 40?°C. The combined results suggested that nanoemulsion may hold an alternative for enhanced and sustained topical delivery system for amphotericin B.     

Study of structural and magnetic properties of (Co–Cu)Fe2O4/PANI composites

The nanocomposites of the polyaniline and Co_1−xCu_xFe₂O₄ (PANI/CoCuFe) were prepared by in-situ oxidative polymerization of aniline. Prepared nanocomposites samples were characterized by using various experimental techniques like X-ray diffraction (XRD), Fourier transformed infrared spectroscopy (FT-IR), field emission scanning electron microscope (FE-SEM), vibrating sample magnetometer (VSM), Mössbauer spectroscopy and ultraviolet–visible spectrophotometry (UV–VIS). The elemental analysis as obtained from the energy dispersive X-ray spectroscopy (EDAX) measurement is in close agreement with the expected composition from the stoichiometry of the reactant solutions. XRD result confirms that all the samples have the single phase cubic spinel structure. Unit cell parameter ‘a’ is found to decrease with the increase in copper ion substitution. The crystallite size was investigated by using the Debye–Scherer formula and it was found in the range of ∼28–37 nm. FE-SEM confirmed the homogeneous and well defined surface morphology of the synthesized samples. FT-IR study showed the main absorption bands corresponding to the spinel structure those arose due to the tetrahedral and octahedral stretching vibrations. Cation distribution was estimated using XRD data. Hysteresis measurements revealed that the saturation magnetization decreased with increase in Cu²⁺ substitution. Magnetic environment of ⁵⁷Fe in Cu-doped cobalt ferrite was investigated by using Mössbauer spectroscopy. Mössbauer study evidenced the ferrimagnetic behavior of the synthesized samples.     

Physico-chemical studies of amorphous carbon nanotubes synthesized at low temperature

This work provides better understanding on the nature of amorphous carbon nanotubes, which are synthesized via a simple chemical route. Amorphous carbon nanotubes (α-CNTs) are successfully synthesized by heating a mixture of ferrocene and ammonium chloride at temperature as low as 200 °C and are treated with hydrochloric acid. Transmission and field emission scanning electron microscopy techniques are performed to examine the morphology and dimension of the samples. X-ray diffraction tests confirm the amorphous structure of the nanotubes. The Fourier transform infrared spectroscopy and Raman studies indicate that the treated α-CNTs consist of many defective walls and are more amorphous compared with the untreated α-CNTs. Ultraviolet–visible absorption studies reveal that the untreated and treated α-CNTs exhibit plasmon absorbance with high bandgaps of 4 eV and 4.35 eV, respectively.     

Adsorptive capacity of spray-dried pH-treated bentonite and kaolin powders for ammonium removal

The effectiveness of ammonium (NH₄⁺) adsorption was investigated, using spray-dried, pH-treated bentonite, and kaolin as adsorbents. Each powder's adsorption capacity towards NH₄⁺ was examined after up to 120 min of sample exposure, and results were compared. The zeta potential values for bentonite samples were between ?1.1 and ?19.4 mV, while for kaolin samples, they were between ?35.7 and ?40.9 mV (pH range examined was 2–10). The adsorption isotherm for bentonite showed a fit with the Langmuir model. The pH 10-treated bentonite and as-received bentonite (dispersed as pH 10 in distilled water) showed the highest adsorption capacity towards NH₄⁺. Meanwhile, for kaolin, the adsorption capacity was low and observed only at low NH₄⁺ concentration (100 mg/L and 200 mg/L), with pH 10-treated kaolin showed the highest adsorption capacity.     

Properties of epoxidized palm oil plasticized polytlactic acid

In this study, epoxidized palm oil (EPO) was utilized as a plasticizer for polylactic acid (PLA) using chloroform as a solvent by solution casting process at six weight ratios of PLA/EPO, 95/05, 90/10, 80/20, 70/30, 60/40, and 50/50, respectively. Fourier-transform infrared (FTIR) spectroscopy was used to identify the functional groups of PLA, EPO, and PLA/EPO blends. Thermal stability, mechanical, and morphological properties of the blends were investigated by thermogravimetric analyzer (TGA), tensile properties measurements, and scanning electron microscope (SEM) technique, respectively. The FTIR spectra indicate that there are some molecular interactions by intramolecular hydrogen bond between PLA and EPO. All sets of PLA/EPO blends show high thermal stability and significant improvement of mechanical properties compare to pure PLA. The highest elongation at break (about 210%) was obtained when the ratio of PLA/EPO blend was 80/20. Morphological results of PLA/EPO blends show that ESO was good miscible with PLA.