Pressure induced transformations in condensed and molecular phases of C60

Solid C₆₀ is known to undergo dimerization under suitable conditions of temperature and pressure. We use a potential model (6-exponential potential) to study the changes leading to the formation of various dimers by hydrostatic pressure on C₆₀ solid at elevated temperatures. We have earlier shown, using Tersoff and Brenner potentials, that a system of two bucky-balls can form a dimer by bonding in different ways, when they start with different orientations at close distances. Based on this, we suggest the required preconditions (P-T curve) for the formation of different dimers from the pristine solid. Stability of the bucky-ball under internal or external pressure has also been studied using Tersoff and Brenner potentials. These two potentials have been compared for their applicability under high pressure conditions as well as for dimerization. We have also estimated the bulk modulus of the bucky-ball at several pressures (under which the molecule remains stable). The values of bulk modulus agree closely with those reported in earlier calculations around zero pressure. When the pressure inside the bucky-ball exceeds 116 GPa, it is seen to break open. This is in close agreement with the findings of molecular dynamics calculations.     

Selective solid-phase extraction of rare earth elements by the chemically modified Amberlite XAD-4 resin with azacrown ether

A selective solid-phase extraction procedure using chemically modified Amberlite XAD-4 with monoaza dibenzo 18-crown-6 ether was investigated for the preconcentration and separation of La(III), Nd(III) and Sm(III) in synthetic solution. Before loading samples on synthesized adsorbent adjust pH 4.5 by suitable buffer solution. The adsorbed rare earth elements were eluted by 2 M hydrochloric acid. Various parameters like preconcentration, breakthrough capacity, flow rate were investigated. The limits of detection (n = 5) and limits of quantification (n = 5) for La(III), Nd(III) and Sm(III) were founded 3.9, 4.2 and 7.4 μg L^?1 and 13, 15 and 26 μg L^?1, respectively. The eluted metal ions were determined by ICP-AES.     

Survival of Salmonella, Escherichia coli O157:H7, and Listeria monocytogenes on Inoculated Almonds and Pistachios Stored at -19, 4, and 24° C

The survival of Salmonella, Escherichia coli O157:H7, and Listeria monocytogenes was determined on almonds and pistachios held at typical storage temperatures. Almond kernels and inshell pistachios were inoculated with four- to six-strain cocktails of nalidixic acid-resistant Salmonella, E. coli O157:H7, or L. monocytogenes at 6 log CFU/g and then dried for 72 h. After drying, inoculated nuts were stored at -19, 4, or 24°C for up to 12 months. During the initial drying period after inoculation, levels of all pathogens declined by 1 to -log CFU/g on both almonds and pistachios. During storage, moisture content (4.8%) and water activity (0.4) of the almonds and pistachios were consistent at -19°C; increased slowly to 6% and 0.6, respectively, at 4°C; and fluctuated from 4 to 5% and 0.3 to 0.5 at 24°C, respectively. Every 1 or 2 months, levels of each pathogen were enumerated by plating; samples were enriched when levels fell below the limit of detection. No reduction in population level was observed at -19 or 4°C for either pathogen, with the exception of E. coli O157:H7-inoculated almonds stored at 4°C (decline of 0.09 log CFU/g/month). At 24°C, initial rates of decline were 0.20, 0.60, and 0.71 log CFU/g/month on almonds and 0.15, 0.35, and 0.86 log CFU/g/month on pistachios for Salmonella, E. coli O157:H7, and L. monocytogenes, respectively, but distinct tailing of the survival curves was noted for both E. coli O157:H7 and L. monocytogenes.     

Preparation of cobalt ferrite from the thermolysis of cobalt tris(malonato)ferrate(III)trihydrate precursor

Thermal decomposition of cobalt tris(malonato)ferrate(III)trihydrate precursor, Co₃[Fe(CH₂C₂O₄)₃]·3H₂O has been investigated from ambient temperature to 600 °C in static air atmosphere using various physico-chemical techniques, i.e. TG–DTG–DSC, XRD, Mössbauer and IR spectroscopic techniques. The precursor undergoes dehydration and decomposition simultaneously to yield cobalt malonate and iron(II) malonate intermediates at 205 °C. At higher temperature (325 °C) these intermediate species undergo exothermic decomposition to yield CoO and α-Fe₂O₃, respectively. Finally cobalt ferrite, CoFe₂O₄, has been obtained as a result of solid–solid reaction between Fe₂O₃ and CoO at a temperature (380 °C) much lower than that of ceramic method. SEM analysis of the final thermolysis product reveals the formation of monodisperse cobalt ferrite nano-particles with an average particle size of 45 nm. Magnetic studies show that these particles have a saturation magnetization of 3095 G and Curie temperature of 504 °C. Lower magnitude of these parameters as compared to the bulk values is attributed to the smaller particle size.     

A study of austenitization of SG iron

Austenitization process of three SG irons with varying compositions and as cast matrix microstructure has been studied at three austenitization temperatures of 850, 900 and 950C for different time periods. Microstructure, hardness and X-ray diffraction have been used to reveal the nature of dependence of the process on austenitization temperature, time and as cast structure. The optimum austenitization time is maximum for ferritic and minimum for pearlitic matrix.     

Optical and electrical characterization of conducting polymer-single walled carbon nanotube composite films

The optical and electrical properties of the conducting polymer poly(3-hexylthiophene) and single walled carbon nanotube (SWCNT) composites have been investigated. The composites were prepared by dispersing carbon nanotubes in the polymer matrix already dissolved in 1,2-dichlorobenzene. The optical absorption, photoluminescence (PL) and electrical conductivity of the composite was studied as a function of SWCNT concentration in the solution. The absorption coefficient of the polymer was found to be unaffected upto a SWCNT concentration 5% w/w. However a minor decrease in the absorption in visible region was observed for higher SWCNT concentrations. The intensity of PL emission from the composite was measured and was found to decrease with the increase in SWCNT concentration. For a SWCNT concentration of 30% w/w, ∼90% of the PL was quenched, indicating an ultra fast transfer of photoinduced charges from donor polymer to acceptor SWCNT. Direct current conductivity of the composite film was found to increase rapidly with the increase in SWCNT concentration and an increase of ∼5 orders of magnitude was observed for a 30% w/w concentration. The enhancement in conductivity is explained in terms of percolation theory with an estimated percolation threshold of 2% w/w.     

An efficacious “naked-eye” selective sensing of cyanide from aqueous solutions using a triarylmethane leuconitrile

A triarylmethane dye 1 detects CN^? from water and shows remarkable selectivity over other anions and dramatic color changes, in solution as well as when dyed. The pH stability of 1 in the range of 1.2–10.7 offers additional advantage in the sensing process under physiological conditions.     

Development of pitch-based carbon–copper composites

Carbon–copper composites with varying copper to carbon ratio of 0.66–1.5 (by weight) were developed from coal-tar-pitch-derived green coke (as such or modified with natural graphite) as carbon source and electrolytic grade copper powder at different heat treatment temperatures (HTTs) of 1000–1400 °C. The physical, mechanical, and electrical properties differ depending upon the HTT and also on copper to carbon ratio (Cu/C). The composites prepared at HTT of 1100 °C having Cu/C ratio of 0.66 and 0.9 exhibited a high bending strength of 150 and 140 MPa, bulk density of 2.63 and 2.81 gm/cm³, electrical resistivity of 1.6 and 0.96 m Ω cm and shore hardness of 88 and 84, respectively, in spite of well-known inadequate wettability between copper and carbon. Increasing the temperature from 1100 °C for processing of the composites deteriorated the properties mainly due to the loss of copper through melting above 1100 °C as revealed by X-ray, scanning electron microscopy, thermal analysis and EDAX studies.