Simultaneous separation of mercury and lignosulfonate from aqueous solution using supported liquid membrane

This paper presents an experimental investigation on facilitated and simultaneous transport of mercury and lignosulfonate (LS) through a flat sheet supported liquid membrane (SLM) having Nylon 6,6 as support, trioctylamine (TOA) as carrier and dichloroethane as solvent. The experiments were performed at various operating conditions such as strip phase concentration, feed pH, carrier concentration and feed concentration to find the best set of parameters that would yield the maximum separation of pure mercury as well as its mixture with LS. The experiments were performed in co-transport mode using NaOH as the strip phase. It was observed that extraction of mercury as well as its mixture increases with increase in concentration of NaOH up to a certain limit 0.1 M NaOH in case of pure solution and 0.2 M NaOH in case of mixture). Feed phase pH significantly affects the mercury separation process. However, initial feed concentration does not affect the extraction process appreciably. Separation of mixture of mercury and LS behaves in a similar way as their pure solution; however the extraction is low in comparison to pure solution. The extraction of mercury from its pure solution is about 81% in 1 h. The extraction of mercury and LS from their mixture is about 52.6% and 50.2%, respectively at optimum condition and in a period of 2 h.     

Montmorillonite K-10 clay catalyzed solvent-free synthesis of bis-indolylindane-1,3-dione, 2-(1′,3′-dihydro-1H-[2,3′]biindolyl-2′-ylidene)-indan-1,3-dione and bisindolylindeno[1,2-b]quinoxaline under microwave irradiation

An environmentally benign protocol has been described for the synthesis of novel 2-(1′,3′-dihydro-1H-[2,3′]biindolyl-2′-ylidene)-indan-1,3-diones/bis-indolylindane-1,3-diones from ninhydrin and 3-substituted/unsubstituted indoles. It uses montmorillonite K-10 as catalyst in a solvent-free condition under microwave irradiation. The method was also used for the synthesis of novel bisindolylindeno[1,2-b]quinoxaline derivatives.     

Biosorbents for hexavalent chromium elimination from industrial and municipal effluents

The presence of hexavalent chromium in wastewater is a potential hazard to aquatic animals and humans. There are various mechanisms proposed, kinetic models used and adsorption isotherms employed for the efficient removal of hexavalent chromium from industrial and municipal wastewaters using biosorbents. Biosorption of heavy metals is a most promising technology involved in the removal of toxic metals from industrial waste streams and natural waters. Metal removal treatment systems using microorganisms are cheap because of the low cost of sorbent materials used and may represent a practical replacement to conventional processes. The present review discusses hexavalent chromium biosorption properties of algae, bacteria, fungi, and agricultural products, as well as adsorption properties of non-living substances. Cell walls are responsible for biosorption of dead biomaterial; compositions of cell walls are discussed. Chemical modification of biosorbents, optimization of biosorption parameters, mixtures of different biosorbents and the study of biosorption mechanisms are the main keys to transfer the biosorption process from lab to industry.     

Functionalized proline with double hydrogen bonding potential: highly enantioselective Michael addition of carbonyl compounds to β-nitrostyrenes in brine

Simple synthetic manipulation of S-proline allows access to prolinamides 5-7 as organocatalysts capable of double hydrogen bonding for enantioselective Michael addition reactions of carbonyl compounds to β-nitrostyrenes. It is shown that prolinamide catalyst 7 leads to addition products with a high diastereo- as well as enantioselectivity. The transition state structure involving the binding of electrophilic nitrostyrene via two H-bonds is believed to be further stabilized by π,π stacking interactions mediated by the tosyl ring.     

Distributed fault-tolerant topology control in wireless multi-hop networks

In wireless multi-hop and ad-hoc networks, minimizing power consumption and at the same time maintaining desired properties of the network topology is of prime importance. In this work, we present a distributed algorithm for assigning minimum possible power to all the nodes in a static wireless network such that the resultant network topology is k-connected. In this algorithm, a node collects the location and maximum power information from all nodes in its vicinity, and then adjusts the power of these nodes in such a way that it can reach all of them through k optimal vertex-disjoint paths. The algorithm ensures k-connectivity in the final topology provided the topology induced when all nodes transmit with their maximum power is k-connected. We extend our topology control algorithm from static networks to networks having mobile nodes. We present proof of correctness for our algorithm for both static and mobile scenarios, and through extensive simulation we present its behavior.     

Molecular interaction of organic dyes in bulk and confined media

Molecular interactions of five thiazine dyes with increasing alkyl substitution have been studied in aqueous and microemulsion media at 303 K within a concentration range of (1.35–7.00) × 10^?4 M. The dimerization constant (K_d) values for the five dyes are ranged between 1.761 and 6.258 × 10³ l mol^?1 in bulk water media, where as in microemulsion media, K_d's are ranged between 1.760 and 4.110 × 10³ l mol^?1. Thionine (with no methyl substitution) and azure A (with two methyl substitution) displayed slightly larger K_d values in microemulsion water pools compared to bulk water while other dyes recorded significant drop in K_d values. The influence of microemulsion media on the molecular interaction of dyes has been explained in terms of electrostatic and hydrophobic factors. The monomer and the dimer spectra are explained in terms of molecular exciton model and the optical absorption parameters of both the species are reported in bulk and confined media.     

Gamma irradiation route to synthesis of highly re-dispersible natural polymer capped silver nanoparticles

Aqueous dispersions of highly stable, redispersible silver nanoparticles (Ag NPs) were synthesized using gamma radiolysis with gum acacia as a protecting agent. The formation of nanosized silver was confirmed by its characteristic surface plasmon absorption peak at around 405 nm in UV–vis spectra. The size of the silver nanoparticles can be tuned by controlling the radiation dose, ratio of gum acacia to silver ions and also the ionic strength of the medium. Dynamic light scattering (DLS) measurement of the as-synthesized nanoparticles indicated the size less than 3 nm at higher dose of radiation and this also corroborated the size measurement from the width of the corresponding X-ray diffraction (XRD) peak. The face centered cubic (fcc) crystallinity of the nanoparticles was evident from XRD and high resolution transmission electron microscopic (HRTEM) measurements. Fourier transform infra-red (FTIR) spectroscopic data indicate a bonding of Ag NPs with COO^? group of acacia through bridging bidentate linkage.     

A simulation study on photoacoustic signals from red blood cells

A two dimensional simulation study was performed to investigate the photoacoustic signal properties of non-aggregated and aggregated erythrocytes. Spatial distributions of non-aggregated blood samples were generated by employing a Monte Carlo method and aggregated blood samples were simulated using a hexagonal packing scheme. For the non-aggregating case photoacoustic signals demonstrated a monotonic rise with hematocrit. For the aggregating case it was found that spectral (<20 MHz) intensity increased (11 dB at 15.6 MHz) when the aggregate size increased. This study strongly suggests that the assessment of erythrocyte aggregation level in human blood might be possible by using a photoacoustic spectroscopic method.     

A simple technique for evaluation of transmission coefficient at the splice with angular offset and transverse offset for first higher mode propagation in graded index fibers

We present simple and accurate analytical expressions for transmission coefficient at the splice with angular offset and transverse offset in case of first higher mode propagation in graded index fibers. We employ the simple series expression for first higher order modal field for graded index fiber. The evaluation of the concerned parameters based on our formalism requires very little computations. Here, we show that our estimations match excellently well with the exact results in case of step and parabolic index fibers. Further, splice being highly tolerant for longitudinal separation, our analysis is judiciously restricted to the case of transverse and angular mismatches only. The analysis should find application in dual mode graded index fiber in all optical technology.     

Electromagnetic field with induced massive term: Case with scalar field

We consider an interacting system of massless scalar and electromagnetic fields, with the Lagrangian explicitly depending on the electromagnetic potentials, i.e., interaction with broken gauge invariance. The Lagrangian for interaction is chosen in such a way that the electromagnetic field equation acquires an additional term, which in some cases is proportional to the vector potential of the electromagnetic field. This equation can be interpreted as the equation of motion of photon with induced nonzero rest-mass. This system of interacting fields is considered within the scope of Bianchi type-I (BI) cosmological model. It is shown that, as a result of interaction the isotropization process of the expansion takes place.