Detection of a sulfur dioxide radio line ν∼131 GHz in the lower troposphere

We present the results of detection of the sulfur dioxide radio line ν∼131 GHz of anthropogenic origin in the lower troposphere emission. The methods and results of spectral radiometric studies of SO₂ content near its sources are described. Institute for Space Research, Moscow; Radiophysical Research Institute, Nizhny Novgorod, Russia. Translated from Izvestiya Vysshikh Uchebnykh Zavedenii, Radiofizika, Vol. 40, No. 6, pp. 704–712, June, 1997.     

AUTOMATED WIND TUNNEL MEASUREMENTS

It is common practice in power transmission to use bundled overhead electrical conductors because the lower rate of corona discharge, compared with single conductors, makes the bundle attractive for high voltages. However, secondary problems may arise from the vibrations induced by the aerodynamic forces which act on the leeward conductors as a result of their immersion in the wake of a windward conductor. Thus, in addition to possible aeolian and galloping oscillations observed for a single conductor, bundle conductors may also be subjected to wake-induced oscillations. ^1,2 Although extensive research has been done on the aeroelastic behavior of single and bundled conductors which are bare, little is known about the galloping or wake oscillation characteristics of given bundle conductors which, depending upon the environmental conditions during the formation of ice, may have five or so representative shaped cross-sections. One important task involves the aerodynamic quasi-static force and moment measurements in a wind tunnel using full scale conductor cross-sections each of which must be rotated through many angles at different spacings. Such measurements are repetitive as well as tediously time consuming and, hence, are beneficially automated. A reliable, accurate and inexpensive automated apparatus is described in this paper which permits the aerodynamic measurements to be performed efficiently and without intervention. Most importantly, it relieves the operator of the usual responsibility for manually controlling the separation and orientation of the sections as well as the need to manually compensate fluctuations in the free stream air speed. For simplicity, the apparatus is detailed in the context of a twin bundle conductor.     

Fiber formation via solution spinning of the cellulose/ammonia/ammonium thiocyanate system

Fiber formation via the cellulose/ammonia/ammonium thiocyanate system by wet spinning has been investigated. This report presents a characterization of the structure and tensile properties of fibers spun under various coagulation conditions. Microscopic observations showed that the molecular size of coagulant was the dominant factor governing the crosssectional shape of the fibers. Density, birefringence, and crystallinity data indicated that a higher cellulose concentration and lower coagulation temperature favored development of a fiber with a denser and more oriented structure. Under optimum conditions, a welldefined fibrillar structure was obtained. Fiber tensile property measurements suggested the existence of a linear relationship between the fiber breaking tenacity and the product of the square of the Hermans' orientation factor and the infrared crystallinity index.     

The binding of manganese(II) and zinc(II) to the synthetic oligonucleotide d(C-G-C-G-A-A-T-T-C-G-C-G)2. A 1H NMR study

The interaction of the synthetic oligonucleotide d(C-G-C-G-A-A-T-T-C-G-C-G)2 with two different transition-metal ions has been investigated in aqueous solution by means of 1H NMR spectroscopy. The effects on the DNA due to the presence of manganese(II) or zinc(II) have been monitored by observing the paramagnetic broadening and diamagnetic shifts of the non-exchangeable proton resonance lines, respectively. The 1H NMR spectra acquired during the course of the manganese(II) titration show very distinct broadening effects on certain DNA resonance lines. Primarily, the H8 resonance of G4 is affected, but also the H5 and H6 resonances of C3 are clearly affected by the metal. The results imply that the binding of manganese(II) to DNA is sequence specific. The 1H spectra obtained during the zinc(II) titration reveal diamagnetic shift effects which largely conform with the paramagnetic broadening effects due to the presence of manganese(II), although this picture is somewhat more complex. The H8 resonance of G4 displays a clearly visible high-field shift, while for the other guanosine H8 protons this effect is absent. The H1' and H2' protons of C3 show an effect of similar strength, although in the opposite direction, while H5 and H6 of C3 are only slightly affected. Local differences in the structure of the DNA and the basicities of potential binding sites on different base steps in the sequence might account for the observed sequence selectivity.     

Four unit linking groups IV. Liquid crystals of positive dielectric anisotropy

Three separate series of new materials of weak to strongly positive dielectric anisotropy have been prepared. Each series contains four sub-sets of materials each incorporating a different four unit linking group (i.e., C₄H₈, C₄H₆, C₃H₆O and C₃H₄O) and the same series of end groups (i.e. F, CN and OCF₃) in various substitution patterns. The synthesis and liquid crystal transition temperatures of these novel substances are described and compared with those of the corresponding materials incorporating standard central linkages (i.e.-, C₂H₄, CH₂O, COO). The effect of an additional trans carbon-carbon double bond in the terminal alkyl chain and in the central linking unit has also been studied.     

Identification of peroxyacetic acid uroporphyrin I in the urine of patients with congenital erythropoietic porphyria by liquid chromatography and mass spectrometry

A new porphyrin, peroxyacetic acid uroporphyrin I, has been isolated from the urine of patients with congenital erythropoietic porphyria by reversed phase high performance liquid chromatography. The porphyrin was characterized by high resolution mass spectrometry and by typical chemical reactions of a peroxyacid.     

The oxidation of 3,3′-dimethoxy benzidine with potassium bromate in acidic solutions

The kinetics and mechanism of the oxidation of 3,3′-dimethoxybenzidine (oda, o-dianisidine) by potassium bromate in aqueous acidic medium were studied by monitoring the formation rate of the reaction product, 3,3′-dimethoxy 4,4′-diphenoquinone at 447 nm. The reaction is, first order with respect to both the substrate and oxidant, and second order with respect to H⁺. The oda: bromate stoichiometric ratio is 1:1. Plausible mechanism and rate laws are proposed accounting the experimental findings. Computer simulations were done using the proposed mechanism.     

The contribution of the (t(τ)+N) component to the α-particle wave function from data on the reactions p(α,pp)t and p(α,pn)τ at incident α-particle momentum 5 GeV/c

The 2-meter liquid-hydrogen bubble chamber is exposed to a separated beam of α particles from the ITEP synchrotron. The momentum of the incident ⁴He nuclei, averaged over the fiducial volume of the chamber, is 5 GeV/c (the kinetic energy of initial protons in the nucleus rest frame is T _p =620 MeV). The spectral functions of decays α→tp and α→τn) are extracted in the 4π geometry (the latter is extracted for the first time) from the exclusive reactions αp→tpp and αp→τpn in the spectator momentum region 0<q<0.3 GeV/c. The pole dominance criteria are carefully checked. Extrapolation of the nuclear vertex function to the pole gives a lower bound on the nuclear vertex constant. Our experimental data are compared with the results of other studies and with theoretical calculations. Pis’ma Zh. éksp. Teor. Fiz. 66, No. 2, 69–74 (25 July 1997) Published in English in the original Russian journal. Edited by Steve Torstveit.     

Synthesis of dimethylditritiogermane Me<Subscript>2</Subscript>GeT<Subscript>2</Subscript>

A microsynthetic procedure for preparing tritium-labeled alkyl-substituted germanes is developed. The resulting dimethylditritiogermane can be used as a source of dimethylgermylium ions. The synthesis was performed by the reduction of dibromodimethylgermane with lithium tritide in presence of AlBr₃.