Thermal decomposition of ammonium uranates

The thermal decomposition of ammonium uranates precipitated from uranyl nitrate solution on the addition of aqueous ammonium hydroxide and hexamine under various conditions has been studied by means of thermogravimetry, differential thermal analysis, infrared spectroscopy and X-ray diffraction. Although all precipitates show the composition corresponding to UO₃ · NH₃ · H₂O, the precipitates with hexamine give X-ray diffraction patterns designed as types I and II, in which type I is similar to the precipitates with ammonia. As a result, it is concluded that ammonium uranates thermally decompose to amorphous UO₃ at about 400°, and transform to U₃O₈ via-UO₃ and/or-UO₃, latter being formed in the case of type II only.

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Zusammenfassung Die thermische Zersetzung von unter verschiedenen Bedingungen durch wässrige Lösungen von Ammoniumhydroxid und Hexamin aus Uranylnitrat-Lösung gefällten Ammoniumuranaten wurde mittels TG, DTA, IR-Spektroskopie und Röntgendiffraktometrie untersucht. Obwohl die Zusammensetzung aller Niederschläge der Formel UO₃ · NH₃ · H₂O entspricht, geben die mit Hexamin gefällten Niederschläge die als Typ I und II bezeichneten Röntgendiffraktogramme, von denen das des Typs I ähnlich dem der mit Ammoniak gefällten Niederschlage ist. Es wird festgestellt, daß Ammoniumuranate bei 400° thermisch zu amorphen UO₃ zersetzt werden und sich über-UO₃ und/oder-UO₃—wobei beim Typ II nur das letztere gebildet wird — in U₃O₈ umwandeln.

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, , - - , . @2 UO₃ · NH₃ · H₂O, , - I II. . , 400° UO₃ U₃O₈ -UO₃ -UO₃. II.

     

Photosensitive organosilicon polymers for microlithographic application

Two new families of photosensitive organo-silicon polymers are described. One is based on the Si-Si σ-bond photochemistry and another is based on the combinations of new alkaline-soluble organosilicon polymers with diazoquinone photosensitizers. Both of these photoactive materials not only give positive photoresist formulations but can act as oxygen reactive ion etch masks in the double-layer resist scheme to finally offer steep submicrometer organic patterns with high aspect ratio.     

Direct imaging of spatially modulated superfluid phases in atomic fermion systems

It is proposed that the spatially modulated superfluid phase, or the Fulde-Ferrell-Larkin-Ovchinnikov state could be observed in resonant fermion atomic condensates which are realized recently. We examine optimal experimental setups to achieve it by solving the Bogoliubov-de Gennes equation for both idealized one-dimensional and realistic three-dimensional cases. The spontaneous modulation of this superfluid is shown to be directly imaged as the density profiles either by optical absorption or by Stern-Gerlach experiments.     

A phenomenological analysis on γp → π+n, πOp below 1.2 GeV

A phenomenological partial-wave analysis on γp → π⁺n and π^Op reactions has been performed in the energy range 0.25–1.2 GeV with available data, laying special emphasis on the polarization and asymmetry data. A good fit has been obtained.     

Chromatographic preconcentration of copper in environmental and biological samples using 2,4,6-tri(2-pyridyl)-1,3,5-triazine-tetraphenylborate-naphthalene adsorbent

A method was established for the determination of trace amounts of copper using chromatographic preconcentration of copper(I) with 2,4,6-tri(2-pyridyl)-1,3,5-triazine and tetraphenylborate. Copper is quantitatively adsorbed on this adsorbent in the pH range 1.8–10.5 and at flow-rates of 0.2–10 ml/min. The solid mass consisting of copper complex along with naphthalene is dissolved from the column with 5 ml of dimethylformamide. A calibration curve is obeyed over the concentration range 0.2–10.0 g of copper in 5 ml of dimethylformamide. Eight replicate determinations of 3 g of copper gave a mean absorbance of 0.185 with a relative standard deviation of 1.4%. The characteristic concentration for 1% absorption is 0.0143 g/ml (0.103 gmg/ml for direct AAS in aqueous medium). The interference of various ion and salts has been studied and the proposed method has been employed to the determination of copper in biological and water samples.     

Redox-based spin diversity in a 6-oxophenalenoxyl system: generation,ESR/ENDOR/TRIPLE,and theoretical studies of 2,5,8-tri-tert-butylphenalenyl- 1,6-bis(olate) salts

[reaction: see text] Novel open-shell molecular salts, 2,5,8-tri-tert-butylphenalenyl-1,6-bis(olate) salts, were designed on the basis of the 6-oxophenalenoxyl system and generated by the chemical reduction of 6-hydroxyphenalenone derivatives. ESR/ENDOR/TRIPLE measurements and DFT calculations provide unequivocal determination of the structure and spin density distribution, which demonstrate redox-based spin diversity of the 6-oxophenalenoxyl system.     

Electrospun nanofiber membranes from polysulfones with chiral selector aimed for optical resolution

Polysulfones with three types of alanyl residue, such as N-α-acetylalanine (Ac-Ala-OH), N-α-benzoylalanine (Bzo-Ala-OH), and N-α-benzyloxycarbonylalanine (Z-Ala-OH), as chiral selectors were prepared by polymer reaction. The resulting modified polysulfones showed chiroptical properties, indicating that the chiral selector residues were successfully introduced into the polysulfone. Nanofiber membranes prepared from the polymeric materials showed adsorption selectivity toward mixtures of racemic Glu, which were adopted as model racemates. Flux values for the nanofiber membranes were enhanced two to three orders of magnitude in comparison with the corresponding typical membranes, but without reduction in permselectivity. In the present study, it is shown that nanofiber is a suitable membrane form not only for molecularly imprinted membranes, but it exhibits enhanced throughput in comparison with typical dense membranes without concurrent reduction in permselectivity.     

Highly phosphonated poly(N‐phenylacrylamide) for proton exchange membranes

A novel highly phosphonated poly(N‐phenylacrylamide) ( PDPAA ) with an ion‐exchange capacity (IEC) of 6.72 mequiv/g was synthesized by the radical polymerization of N‐[2,4‐bis(diethoxyphosphinoyl)phenyl]acrylamide ( DEPAA ), followed by the hydrolysis with trimethylsilyl bromide. Then, the crosslinked PDPAA membrane was successfully prepared by the electrophilic substitution reaction between the aromatic rings of PDPAA and the carbocation formed from hexamethoxymethylmelamine (CYMEL) as a crosslinker in the presence of methanesulfonic acid. The crosslinked PDPAA membrane had high oxidative stability against Fenton's reagent at room temperature. The proton conductivity of the crosslinked PDPAA membrane was 8.8 × 10^?2 S/cm at 95% relative humidity (RH) and 80 °C, which was comparable to Nafion 112. Under low RH, the crosslinked PDPAA membrane showed the proton conductivity of 1.9 × 10^?3 and 4.7 × 10^?5 S/cm at 50 and 30% RH, respectively. The proton conductivity of the crosslinked PDPAA membrane lied in the highest class among the reported phosphonated polymers, and, consequently, the very high local concentration of the acids of PDPAA (IEC = 6.72 mequiv/g) achieved high and effective proton conduction under high RH. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2010     

Mechanism of mode selection in Rayleigh—Bénard convection with free—rigid boundaries

Higher harmonic resonances with wavenumber ratio of 1:2, 1:2:3 and so on are shown to take place in Rayleigh—Bénard convection under free—rigid boundary condition. Bifurcation diagrams for two-dimensional motion are obtained for the Prandtl number P = 7. The subharmonic instability is explained by a couple of amplitude equations obtained from weakly nonlinear stability theory. A straightforward extension of the coupled amplitude equations leads to a model which consists of n amplitude equations. The mechanism of mode selection is illustrated by numerical simulations of the model equations.     

The effect of atmospheric plasma treatments on plastic scintillator for beta-ray measurement

A plastic scintillator (PS) can be used for beta-ray measurements using a liquid scintillation counter (LSC) without the necessity for a liquid scintillator when liquid samples of beta-emitters are placed on the PS. However, the measurement efficiency with the PS in this study was not high, especially in the case of tritium. With a sample of tritiated water, a long measurement time was necessary with a conventional LSC. However, the measurement efficiency was improved drastically by modifying the PS surface with atmospheric-pressure glow-plasma processing (the plasma method). A 2 Bq, 20 μL sample of tritiated water placed between two PS sheets was successfully measured within 2 min by an LSC. The measurement efficiency was same as that of using liquid scintillator: 48 ± 2 % for tritiated water. The measurement efficiency was initially increasing over time, and after almost 6 h, it plateaued and remained at a constant value for several weeks. Additionally, the measurement efficiency of the plasma-modified PS was identical when it was used soon after the treatment and after being properly stored for 1 week The results show that plasma-modified PS can be used stably after storage in a freezer or a deep freezer. The plasma method is advantageous because it produces little radioactive waste fluid. This paper presents these results and the results of an investigation of the surface of the plasma-modified PS under observation with an atomic force microscope, and the mechanism behind the high measurement efficiency is discussed.