Study of the reactione + e −→K + K − in the energy range1350 \leqq \sqrt s \leqq 2400 MeV

Thee ⁺ e ^?→K ⁺ K ^? cross section has been measured from about 750 events in the energy interval \(1350 \leqq \sqrt s \leqq 2400 MeV\) with the DM2 detector at DCI. TheK ^± form factor |F _F ^±| cannot be explained by the ρ, ω, ? and ρ′(1600). An additional resonant amplitude at 1650 MeV has to be added as suggested by a previous experiment.     

Aqueous Solutions of Colloidal Ruthenium: the Radiation–Chemical Preparation and Optical Absorption

The radiation-chemical reduction of Ru(III) is studied in aqueous RuCl₃ solutions containing isopropyl alcohol. In the presence of sodium polyacrylate, the stable sols of metal are formed with spherical particles 4–8 nm in diameter. The optical spectrum of nanoparticles is characterized by an increasing absorption in the UV spectral region with no maximum (₂₀₀ = 7.2 × 1030 l mol^–1 cm^–1). The colloids of ruthenium in an aqueous solution are stable in the open air.     

Electrochemical,Structural, and Thermogravimetric Studies of Activated Supercapacitor Electrodes Based on Carbonized Cellulose Cloth

Russian Journal of Physical Chemistry A - The high–temperature reagentless activation of carbonized cellulose cloth is used to manufacture supercapacitor (SC) electrodes with different fast...     

Sorption of Cu2+ ions by chitin and chitosan from aqueous solutions. Molecular structure of complexes formed

The sorption of Cu²⁺ ions by chitin and chitosan from aqueous solutions has been investigated, as well as the molecular structure of the complexes formed. The static exchange capacities have been determined, equal to 3.5 and 0.25 mmole/g for chitosan and chitin, respectively, and the partition coefficients (5000 and 70 g/ml). It has been shown that in complex formation a bond with the amino group is formed as the result of the substitution of a proton in the latter. The EPR spectra of these complexes have been obtained and their radiospectroscopic parameters determined (g = 2.334,g = 2.054,A = 0.0156 cm^–1, andB = 0.0028 cm^–1 for chitin, andg = 2.231,g = 2.048,A = 0.0192 cm^–1, andB = 0.0025 cm^–1 for chitosan). For chitosan the ligands are two nitrogen atoms of the amino groups and two oxygen atoms of the hydroxyl groups in the position C³ of adjacent glucosamine rings; for chitin, the oxygen atoms of the acetyl groups take part in addition in the complex formation. The analysis of the radiospectroscopic parameters and their comparison with published data lead to the conclusion that the Cu²⁺ complex with chitosan has a tetragonal symmetry, while the complex with chitin most probably has an octahedral structure.Institute of Physical Chemistry, Russian Academy of Sciences, 117915 Moscow. Translated from Izvestiya Akademii Nauk, Seriya Khimicheskaya, No. 10, pp. 2305–2311, October, 1992.     

Sonolysis of metal beta-diketonates in alkanes

The kinetics of metal beta-diketonates sonolysis was studied in hexadecane solutions using a UV/VIS spectrophotometric technique. The following complexes were prepared and studied: Cu(HFAA)(2), Cu(DPM)(2), Fe(ACAC)(3), Ni(DPM)(2), Er(DPM)(3), Nd(DPM)(3), Th(DPM)(4), UO(2)(BTFA)(2).TOPO, and Np(HFAA)(4), where HHFAA is hexafluoroacetylacetone, HDPM is dipivaloylmethane, HACAC is acetylacetone, HBTFA is benzoyltrifluoroacetone, and TOPO is trioctylphosphine oxide. Sonolysis was performed under the following conditions: ultrasonic frequency 22 kHz, intensity of ultrasound 3-5 Wcm(-2), temperature 70-92 degrees C, Ar atmosphere. The kinetic behavior of the studied complexes are interpreted using a two-site model of the sonochemical processes. In the case of metal beta-diketonates with high vapor pressure the sonochemical reactions tend to occur in the gaseous phase of the cavitating bubbles. The sonolysis of less volatile complexes first occur in the liquid reaction zone surrounding the bubbles. Sonication of the studied complexes results in the formation of X-ray amorphous products consisted of a mixture of metal beta-diketonates partial degradation products. Heating of as-prepared sonication products in air yields nanocrystalline oxides of corresponding metals.     

Radiative decay ofJ/ψ into γ π+ π−

The radiative decayJ/ψ → γ π⁺ π^? has been studied using the 8.6 millionJ/ψ produced in the DM2 experiment at the DCIe ⁺e^? storage rings at Orsay. The π⁺ π^? mass spectrum shows a cleanf ₂ (1270) signal, and the possible presence of two other states at thef ₂ (1720) andf ₄ (2030) masses. For thef ₂ (1270), the branching ratio BR(J/ψ →γf)xBR(f→π⁺ π^?) is measured to be (7.50±0.30±1.12)×10^?4, and the spin analysis prefers theJ=2 assignment, with helicity parametersx=0.83±0.06 andy=0.01±0.06. The existence of higher mass states is discussed.     

Isomers of astrophysical interest in neutron-deficient nuclei at masses A = 81, 85 and 86

Decay properties of neutron-deficient exotic nuclei close to A=80 have been investigated at the IGISOL facility. The studied nuclei, ⁸¹Y, ⁸¹Sr, ^81mKr, ⁸⁵Nb, ⁸⁵Zr, ⁸⁶Mo and ⁸⁶Nb, were produced by a ³²S beam from the Jyv?skyl? isochronous cyclotron on ⁵⁴Fe and ^natNi targets. The internal conversion coefficient for a 190.5 keV isomeric transition in ^81mKr has been measured and the internal transition rate has been determined. The internal transition rate has been used to estimate a neutrino capture rate on ⁸¹Br, which yields a log ft of 5.13±0.09 for the reaction ⁸¹Br( ν, e ^-)^81mKr. A new isomer with a half-life of 3.3±0.9 s has been observed in ⁸⁵Nb. The existence of an earlier reported isomer with a half-life of 56 s in ⁸⁶Nb has not been confirmed.