N. Dharmaraj

UV-visible spectroscopic estimation of photodegradation of rhodamine-B dye using tin(IV) oxide nanoparticles

Nanocrystalline, tin(IV) oxide (SnO(2)) particles has been prepared by thermal decomposition of tin oxalate precursor obtained from the reactions of tin(IV) chloride and sodium oxalate using eggshell membrane (ESM). The as-prepared SnO(2) nanoparticles were characterized by thermal studies, transmission electron microscopy (TEM), powder X-ray diffraction (XRD), Raman, FT-IR and UV-visible studies and used as a photocatalyst for the degradation of rhodamine-B (Rh-B) dye. The size of the prepared nanoparticles was in the range of 5-12nm as identified from the TEM images. Powder XRD data revealed the presence of a tetragonal, rutile crystalline phase of the tin(IV) oxide nanoparticles. Thermal analysis showed that the decomposition of tin oxalate precursor to yield the titled tin(IV) oxide nanoparticles was completed below 500°C. The extent of degradation of Rh-B in the presence of SnO(2) monitored by absorption spectral measurements demonstrated that 94.48% of the selected dye was degraded upon irradiation with UV light for 60 min.

Spectroscopic investigations on the photodegradation of toluidine blue dye using cadmium sulphide nanoparticles prepared by a novel method

A novel method to prepare cadmium sulphide nanoparticles (CdS NPs) possessing nearly uniform size was adopted using eggshell membrane (ESM), under different pH conditions. Significant yield of CdS NPs with smallest possible size was obtained by increasing the pH of the reaction medium from acidic to alkaline. The above prepared CdS NPs have been characterized by UV-vis absorption as well as emission spectra, powder X-ray diffraction, scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The efficiency of the above prepared CdS NPs as a catalyst for the photodegradation of toluidine blue (TB) dye, as a function of pH as well as the ratio between the catalyst and the substrate was studied after irradiation with UV light. The results showed that an efficient interaction took place between the catalyst and the substrate to cause degradation of the selected dye. A maximum degradation of toluidine blue dye (90%) was observed at pH 8 which is higher than that of the efficiencies at pH 4 and pH 6.

Effect of sintering temperature on structural and optical properties of indium(III) oxide nanoparticles prepared with Triton X-100 by hydrothermal method.

Indium(III) hydroxide (In(OH)3) powders prepared via Triton X-100 mediated hydrothermal method was sintered at different temperatures (400, 500 and 600°C) to yield indium(III) oxide nanoparticles (In2O3 NPs). Thermal studies of In(OH)3 confirmed complete conversion to In2O3 around 400°C. Powder X-ray diffraction (XRD) pattern of sintered In2O3 nanoparticles revealed the formation of phase pure cubic In2O3. The crystallite size of In2O3 NPs was increased from 12 to 26nm upon increasing the sintering temperature from 400°C to 600°C, while the percentage crystallinity was increased up to 90% after sintering at 600°C. A red shift in the band gap energy was observed with increasing sintering temperature due to the larger size of sintered In2O3 NPs. Room temperature photoluminescence spectra of the indium oxide nanoparticles showed both near band and excitonic emission of In2O3 due to oxygen vacancies.

Antimicrobial drug release scaffolds of natural and synthetic biodegradable polymers

A series of biodegradable polymeric scaffolds was prepared by using a combination of natural (collagen) and synthetic (poly(caprolactone)) (PCL) polymers in various compositions. These scaffolds were soft, spongy, porous and transparent in nature and were characterized by thermogravimetric analysis (TGA) and Fourier transform infrared (FT-IR) spectroscopy. The entrapment efficiency and drug release activity of the scaffolds were analyzed using penicillin and tetracycline as antimicrobial drugs. The drug release activity of the scaffolds with various combinations of collagen and PCL were studied by measuring the optical density in a spectrophotometer at the following time intervals: 1, 4, 24, 48 and 60 h. These scaffolds showed better and continuous drug release for up to 60 h. Even after such a long duration, a portion of the drug remained entrapped in the scaffolds, indicating that they can be utilized for wound healing applications.

Oxygen Sensing Properties of Platinum Doped Indium Oxide Nanoparticles Prepared by Hydrothermal Method

Indium oxide (In2O3) and platinum doped (in situ method) indium oxide (Pt-In2O3) nanoparticles were prepared by surfactant assisted hydrothermal route followed by calcination at 400°C. The X-ray diffraction data revealed that the average size of the nanoparticles was around 15 nm and the transmission electron microscopic investigation showed that the nanoparticles were formed as short nanorods. The oxygen sensing ability of the sensors fabricated using both undoped and Pt-doped In2O3 was found to be higher in the case of later and the maximum was observed at 270°C. Both the sensors showed a linear response to oxygen partial pressures in the measured range from 2.5% to 20%.