Inclusive ϕ production inK − p interactions at 110 GeV/c and search for structure in φ π−

Results on inclusive ? production inK ^? p interactions at 110 GeV/c are presented. The production cross section is found to be larger than in πp andpp interactions at similar energies, suggesting OZI allowed \(s\bar s\) fusion to be the dominant mechanism in ? production. Thex distributions of ? and \(\bar K^{*0} \) are found to be similar to each other over the entirex range suggesting an overall strangeness suppression factor of 0.20±0.04 in the sea to be the dominant source of the difference in the cross section for ? and \(\bar K^{*0} \) . There is no evidence of a narrowφπ ^? state around 2.1 GeV/c² as suggested byK ⁺ experiments, but there is some excess of events in the region 1.94?1.98 GeV/c² consistent with theF-meson mass as observed ine ⁺ e ^? experiments.     

Determination of traces of palladium using radioactive zinc dithizonate as a reagent

A radioreagent method for the analysis of traces of palladium using radioactive zinc dithizonate as the reagent has been developed. The method is rapid, highly selective and palladium concentration down to 2 g present in 10 ml solution can be measured.     

Studies on the extraction behaviour of plutonium(IV) from mixed aqueous-organic media with sulphoxides

Extraction behaviour of plutonium (IV) from nitric acid media by two long-chain aliphatic sulphoxides, namely, di-n-hexylsulphoxide and di-n-octylsulphoxide has been investigated in the presence of several water-miscible organic solvents to study their possible synergistic effect on metal ion extraction. Methanol, ethanol, n-and iso-propanol, dioxane, acetone as well as as acetonitrile were used as the organic component of the mixed (polar) phase. These additives affected the extraction to varying degrees. Thus, extractability of Pu increases 2–3 fold with increasing concentration (upto 20%) of acetonitrile, acetone, methanol and ethanol while it decreases with increasing concentration of n-and isopropanol. At high concentration of the former, synergism changes into antagonism. Possible reasons for such behaviour are briefly discussed. Among these organic additives, maximum enhancement in the extraction of Pu(IV) was observed in the presence of acetonitrile. The relative increase in extraction was found to be more at lower sulphoxide concentrations.     

Substitutions of coordinated salicylaldehyde and its Schiff bases

Summary Several bis/tris-salicylaldehyde, salicylaldimine and salicyalethylenediimine chelates of cobalt(III), chromium(III), cobalt(II), nickel(II) and copper(II) readily react with various brominating agents and undergo α-bromo/cyano/succinimido substitution, with or without accompanying bromine substitution of the aryl ring. The selectivity of these reactions on the metal-coordinated salicylaldehyde derivatives allows the preparation in 50–80% yield of hitherto unreported specific α-bromo products. The substituted organic compounds could be isolated by demetallation of the chelate products.     

Purification of monoclonal antibodies from cell culture supernatants using a modified zirconia based cation-exchange support

A method suitable for the isolation of monoclonal antibodies (Mabs) is described. The protocol utilizes a zirconia based column modified with ethylenediamine-N,N'-tetra(methylenephosphonic) acid to create a novel cation-exchange chromatographic support. Initial experiments using a linear salt gradient demonstrate the ability of this support to efficiently separate Mab from transferrin and bovine serum albumin in a model matrix. Results of the purification of Mab from an actual cell culture supernatant over a range in protein concentrations are also shown. Analyses by enzyme-linked immunosorbent assay and gel electrophoresis demonstrate that Mabs can be recovered from a cell culture supernatant at high yield (92-98%) and high purity (> 95%) in a single chromatographic step.     

Determination of Se,Cd, and Hg in an aquatic environment of Bombay by substoichiometric neutron activation analysis

The toxicity of Se, Cd, and Hg as environmental pollutants and the impact of these elements on the aquatic ecosystem is undisputed. The present paper reports an investigation of the concentration of Cd, Se, and Hg in an aquatic environment of a large metropolitan city like Bombay. As the toxicity of these elements manifests itself at micro and submicro levels, the very sensitive technique of neutron activation analysis was employed. A sequential substoichiometric extraction technique for the separation of radiochemically pure²⁰³Hg,⁷⁵Se, and^115–115mCd from the neutron irradiated target has also been employed.     

Extraction behavior of uranium(VI), plutonium(IV), zirconium(IV), ruthenium(III) and europium(III) with γ-pre-irradiated solutions of N,N′-methylbutyl substituted amides in n-dodecane

The extraction of plutonium(IV), uranium(VI), zirconium(IV), europium(III) and ruthenium(III) with -pre-irradiated n-dodecane solutions of methylbutyl substituted hexanamide (MBHA), octanamide (MBOA) and decanamide (MBDA) from 3.5M HNO₃ has been studied as a function of absorbed dose up to 184×10⁴ Gray. The distribution ratios (K_d) of uranium(VI) decreased gradually up to a dose of 50×10⁴ Gray and became almost constant thereafter, while ruthenium(III) and europium(III) were not extracted in the entire dose range studied. The K_d values of Pu(IV) decreased gradually up to 10×10⁴ Gray, for MBOA, and 30×10⁴ Gray for MBHA and MBDA and then increased up to a dose of 72×10⁴ Gray, indicating the synergistic effect of radiolytic products at higher doses. The extraction of zirconium(IV) was found to increase gradually up to 72×10⁴ Gray. However, the steep fall in K_d values of plutonium(IV), zirconium(IV) beyond a dose of 72×10⁴ Gray was atrributed to third phase formation. The radiolytic degradation of amides was monitored by quantitative IR spectroscopy and was found to follow the order MBOA>MBDA>MBHA at 184×10⁴ Gray having the amines and carboxylic acids as the main radiolytic products.     

Computation of density of perfluoroalkyl methacrylates: a molecular modeling approach

Molecular dynamics simulations have been carried out on different perfluoroalkyl methacrylates to predict their densities. Density calculations on selected perfluoroalkyl methacrylates have been performed using molecular dynamics in the NPT ensemble by employing COMPASS force field. The calculated density values compared quite well with the experimental data reported in the literature.     

Reversible protein adsorption and bioadhesion on monolayers terminated with mixtures of oligo(ethylene glycol) and methyl groups

Surface-grafted, environmentally responsive polymers have shown great promise for controlling adsorption and desorption of macromolecules and cells on solid surfaces. In the paper, we demonstrate that certain mixed self-assembled monolayers (SAMs) of oligo(ethylene glycol) (OEG) and methyl-terminated alkanethiolates on gold form surfaces with switchable hydrophobicity and tendency for protein adsorption and cellular attachment. At temperatures above 32 degrees C, SAMs with a surface density of approximately 50% OEG adsorbed significant amounts of pyruvate kinase and lysozyme, whereas below this temperature, these same SAMs were resistant to the adsorption of these proteins. Furthermore, protein layers adsorbed to these SAMs above 32 degrees C were removed upon rinsing with water below this temperature. Similar results were seen for attachment and release of the marine bacterium, Cobetia marina. The change from nonresistance to adsorptive state of the SAMs was concomitant with a change in advancing water contact angle. Vibrational sum frequency generation spectroscopy suggests that the temperature-induced changes coincide with a disorder-to-partial order transition of the hydrated methylene chains of the OEG moieties within the SAMs. Mixed OEG-methyl SAMs represent both a convenient means of controlling macromolecular and cellular adsorption within the laboratory and a useful tool for relating adsorption properties to molecular structures within the SAMs.