Effect of electron beam irradiation on chemically synthesized nanoflake-like CdS electrodes for photoelectrochemical applications.

In this paper, we chemically synthesized interconnected nanoflake-like CdS thin films for photoelectrochemical solar cell applications and subsequently irradiated them with electron beam irradiation at various doses of irradiation. The as-synthesized and irradiated samples were characterized by means of X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), high-resolution transmission electron microscopy (HR-TEM), and electrochemical measurements. XRD and XPS results confirmed the formation of CdS with a hexagonal crystal structure. FE-SEM and HR-TEM studies confirmed the photoelectrochemical performance, which was dependent on the surface morphology. The calculated values for efficiency demonstrated an outstanding photoelectrochemical performance with a fill factor of 0.38 and efficiency of 3.06% at 30 kGy. The high photoelectrochemical performance may be due to the interconnected nanoflake-like nanostructure and higher active surface area of the CdS samples. These results show that the electron beam irradiation is capable as an electrode for photoelectrochemical solar cells.

Biogenic synthesis of multi-applicative silver nanoparticles by using Ziziphus Jujuba leaf extract.

Herein, we are reporting for the first time one step biogenic synthesis of silver nanoparticles (AgNPs) at room temperature by using Ziziphus Jujuba leaf extract as a reducing and stabilizing agent. The process of nanoparticles preparation is green, rapid, environmentally benign and cost effective. The synthesized AgNPs were characterized by means of UV-Vis., XRD, FT-IR, TEM, DLS and Zeta potential. The absorption band centered at λmax 434 nm in UV-Vis. reflects surface plasmon resonance (SPR) of AgNPs. XRD analysis revealed, that biosynthesized AgNPs are crystalline in nature with the face centered cubic structure. FT-IR analysis indicates that nanoparticles were capped with the leaf extract. TEM images shows the synthesized nanoparticles are having different shapes with 20-30 nm size. The data obtained from DLS that support the hydrodynamic size of 28 nm. Zeta potential of -26.4 mV indicates that the nanoparticles were highly stable in colloidal state. The effect of pH, quantity of leaf extract and concentrations of AgNO3 were also studied to attend control over the particle size and stability. The synthesized AgNPs shows highly efficient catalytic activity towards the reduction of anthropogenic pollutant 4-nitrophenol (4-NP) and Methylene Blue (MB) for environmental protection. Synthesized AgNPs also exhibited good antimicrobial activity against Escherichia coli.

Preparation of N doped TiO2 via microwave-assisted method and its photocatalytic activity for degradation of Malathion.

We report herein, nitrogen doped TiO2 nanostructure synthesized by simple microwave assisted method, where ammonia was used as hydrolyzing agent. The synthesized nanomaterials were characterized by means of X-ray diffraction (XRD) which demonstrated that N-doped TiO2 is in anatase phase with average crystallite size of 10nm. Doping of N into the lattice of TiO2 was supported by X-ray photoelectron spectroscopy (XPS), Fourier transform-infrared spectroscopy (FT-IR), CHNS analysis, energy dispersive spectroscopy (EDS). The diffuse reflectance spectroscopy (DRS) showed shifting of absorption edge toward the visible region. Thermogravimetric-differential thermal analysis (TGA-DTA) points out N-doped TiO2 nanoparticles are thermally stable. In order to achieve maximum degradation efficiency, the effect of catalyst loading, pH and light sources (UV and sunlight) were studied. A maximum 97% degradation efficiency was achieved under optimized conditions. A 80% reduction in the chemical oxygen demand (COD) was observed after 150min that indicated mineralization of Malathion. The cytotoxicological studies indicate that photocatalytically degraded products were less toxic as compared to Malathion.

Highly active lanthanum doped ZnO nanorods for photodegradation of metasystox.

La-doped ZnO nanorods with different La contents were synthesized by microwave assisted method and characterized by various sophisticated techniques such as XRD, UV-Vis., EDS, XPS, SEM and TEM. The XRD patterns of the La-doped ZnO indicate hexagonal crystal structure with an average crystallite size of 30nm. It was found that the crystallite size of La-doped ZnO is much smaller as compared to pure ZnO and decreases with increasing La content. The photocatalytic activity of 0.5mol% La-doped ZnO in the degradation of metasystox was studied. It was observed that degradation efficiency of metasystox over La-doped ZnO increases up to 0.5mol% doping then decreases for higher doping levels. Among the catalyst studied, the 0.5mol% La-doped ZnO was the most active, showing high photocatalytic activity for the degradation of metasystox. The maximum reduction of concentration of metasystox was observed under static condition at pH 8. Reduction in the Chemical Oxygen Demand (COD) of metasystox was observed after 150min. The cytotoxicological studies of meristematic root tip cells of Allium cepa were studied. The results obtained indicate that photocatalytically degraded products of metasystox were less toxic as compared to metasystox.

Petroleum hydrocarbon residues in the marine environment of Bassein-Mumbai.

The paper reports PHc contamination in water, sediment and biota of the coastal area of Bassein-Mumbai in relation to relatively less polluted sites (Dabhol and Ratnagiri) off the west coast of India. To facilitate inter-comparison three standards have been used though the results are reported in terms of SAM (Residue of Saudi Arabian Mix crude). The concentration of PHc in water off Bassein-Mumbai varies widely (2.9-39.2 microg l(-1)) as compared to the average baseline (2.8 microg l(-1)) with higher values generally confined to creeks and estuaries. The higher concentration of PHc in the bottom water of shallow areas is attributed to the contribution from the sediment-associated petroleum residue. High concentration of PHc in the surficial sediment of inshore area Ratnagiri (107.7 ppm, dry wt) is perhaps the remnants of an oil spill that occurred in the Bombay High region on May 17, 1993. The majority of values of PHc concentration in the surficial sediment of the Bassein-Mumbai region exceed 15 ppm (dry wt) against the expected background (<3 ppm, dry wt) and the trend is indicative of transfer of PHc loads from the inshore areas to the open-shore sediments. The PHc concentration of 0.8-2.6 ppm (dry wt) in sediment deposited prior to the first global commercial use of petroleum in core R5 represents the biogenic background. Based on the period of industrialisation and the horizon of PHc accumulation, a sedimentation rate of 0.2 and 1.0 cm y(-1) respectively is estimated for cores U11 and U12. Substantial increase in the concentration of PHc in sediment after 1950 in cores T8 and T10 correlates well with the establishment of refineries on the western shore of the Thane Creek in 1955-1960. A minor peak in most cores in the top 10 cm sediment probably results from biological transfer of PHc lower into the sediment by benthic organisms. Excess of PHc retained in the sediment of the Bassein-Mumbai region over the biogenic background is estimated at 40,000 t. The PHc residues (1.8-10.8 ppm, wet wt) in fish caught off Bassein-Mumbai do not suggest bioaccumulation.