PHYSIOLOGICAL AND MORPHOLOGICAL CHANGES IN IMMOBILIZED L. PLANTARUM NCIM 2084 CELLS DURING REPEATED BATCH FERMENTATION FOR PRODUCTION OF LACTIC ACID

L. Plantarum NCIM 2084 cells are homofermentative, essentially producing lactic acid as the main end product of glucose fermentation. Prolonged use through repeated batch fermentation with the cells of L. plantarum immobilized on chitosan treated polypropylene matrix showed a shift in the metabolic pathway from the homofermentative to heterofermentative, accompanied by morphological changes in immobilized cells from the normal rod shape to the coccoid shape. These changes appear to be related to a shift in the bacterial cell metabolism, resulting in a decrease in lactic acid yields.     

Removal of Pb(II) ions from aqueous solution by adsorption using bael leaves (Aegle marmelos)

Biosorption of Pb(II) on bael leaves (Aegle marmelos) was investigated for the removal of Pb(II) from aqueous solution using different doses of adsorbent, initial pH, and contact time. The maximum Pb loading capacity of the bael leaves was 104 mg g^?1 at 50 mg L^?1 initial Pb(II) concentration at pH 5.1. SEM and FT-IR studies indicated that the adsorption of Pb(II) occurs inside the wall of the hollow tubes present in the bael leaves and carboxylic acid, thioester and sulphonamide groups are involved in the process. The sorption process was best described by pseudo second order kinetics. Among Freundlich and Langmuir isotherms, the latter had a better fit with the experimental data. The activation energy E_a confirmed that the nature of adsorption was physisorption. Bael leaves can selectively remove Pb(II) in the presence of other metal ions. This was demonstrated by removing Pb from the effluent of exhausted batteries.     

Chemical bath deposition of different phases of copper selenide thin films by controlling bath parameters

In the preparation of copper selenide thin films using chemical bath deposition (CBD) technique, it is observed that the pH of the final reacting mixture is the major factor controlling the composition of the film. Thin films of cubic Cu_2−xSe and tetragonal Cu₃Se₂, of band gaps 2.20 and 2.83 eV, respectively, have been prepared using the CBD technique by adjusting the bath parameters like pH, temperature and the ratio between copper and selenium atoms in the reaction bath. X-ray diffraction analysis is used as the major tool for identification of these phases. The results have been confirmed using XPS, ICP and absorption studies.     

Activation of ethyl acetate over metal substituted MCM-41: application to alkylation and acylation

Al-MCM-41, Fe,Al-MCM-41 and Zn,Al-MCM-41 materials with different silicon to metal ratios were synthesized hydrothermally and characterized by XRD, BET, FT-IR, Acidity measurement by pyridine adsorbed FT-IR spectroscopy, ²⁹Si and ²⁷Al MAS NMR and ESR techniques. The orderly arrangement of mesoporous materials was clearly revealed from the XRD patterns. ²⁹Si and ²⁷Al MAS NMR established the co-ordination environment of silicon and aluminium. Electron paramagnetic resonance (EPR) study confirmed the co-ordination environment of Fe in Fe,Al-MCM-41 framework. The catalytic activity of these materials was evaluated in the vapour phase alkylation and acylation of ethylbenzene with ethyl acetate in the temperature range between 250 and 400 °C. The products were found to be 1,3-diethylbenzene (1,3-DEB), 1,4-diethylbenzene (1,4-DEB), 1,2-diethylbenzene (1,2-DEB), 4-ethylacetophenone (4-EAP) and acetophenone (AP). The reaction products revealed that activation of ethyl acetate is a convenient route for both alkylation and acylation reactions. The order of the catalysts activity for the reaction is found to be Fe,Al-MCM-41 (50) > Fe,Al-MCM-41 (100) > Zn,Al-MCM-41 (50) > Zn,Al-MCM-41 (100) > Al-MCM-41 (50) > Al-MCM-41 (100). In addition to the density of acid sites, the strength of acid sites is also important for this reaction. The effects of temperature, feed ratio, WHSV and time on stream were also examined and the results are discussed.     

Growth of iron diselenide nanorods on graphene oxide nanosheets as advanced electrocatalyst for hydrogen evolution reaction

Advanced electrocatalysts for the fabrication of sustainable hydrogen from water splitting are innermost to energy research. Herein, we report the growth of iron diselenide (FeSe₂) nanorods on graphene oxide (GO) sheets using two-step process viz., simple hydrothermal reduction and followed by wet chemical process. The orthorhombic phase of FeSe₂ incorporated GO nanosheet was developed as a low-cost and efficient electrocatalyst for hydrogen evolution reaction (HER) by water splitting. The phase purity, crystalline structure, surface morphology and elemental composition of the synthesized samples have been investigated by UV–visible absorption spectroscopy (UV–vis), fourier transform-infrared spectroscopy (FT-IR), X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM) and energy dispersive X-ray analysis (EDS). Voltammetry and Tafel polarization methods have been utilized to assess the performance of various weight ratio of GO nanosheet in FeSe₂ nanorods towards H₂ evolution. Detailed electrochemical investigations revealed that the 30% FeSe₂/GO composite showed a tremendous electrocatalytic HER activity in acidic medium with high cathodic current density of 9.68 mA/cm² at η = 250 mV overpotential and with a Tafel slope of 64 mV/dec. The 30% FeSe₂/GO composite offers a high synergistic effect towards HER activity, which is mainly due to high electrochemical active catalytic sites, low charge-transfer resistance and enhanced electrocatalytic performances of H₂ production. The present analysis revealed the possible application of FeSe₂/GO composite as a promising low-cost alternative to platinum based electrocatalysts for H₂ production.     

Energy Sensitive Cluster Level Security Selection Scheme for MANET

Wireless Personal Communications - Most of the current Mobile Ad hoc Network (MANET) nodes are battery powered devices with different processing and data handling capacities. The ratio of sensitive...     

Novel organomodified kaolin/silica hybrid fillers in natural rubber and its blend with polybutadiene rubber

Phosphorylated cashew nut shell liquid prepolymer (PCNSL) was used as an organomodifier for kaolin and the role of the PCNSL-modified kaolin as a reinforcing nanofiller in natural rubber (NR) and its blends with polybutadiene rubber (BR) was studied. The organomodified kaolin was characterized using thermogravimetric analysis, powder X-ray diffraction, Fourier transform infrared spectroscopy (FTIR), high-resolution transmission electron microscopy and scanning electron microscopy. It was found that PCNSL could act as a coupling agent and compatibilizer between kaolin and rubber. Improved physico-mechanical properties were observed at a dosage of 6 phr of the modified kaolin in NR. Blends of NR with BR containing precipitated silica/PCNSL-modified kaolin hybrid filler showed improved tensile properties, tear strength and flex fatigue resistance along with lower heat build-up which could be beneficial for applications such as automobile tire sidewall.