In order to reduce the color quenching in the measurement of tritium in urine by liquid scintillation counting , UV irradiation
was applied to decompose the organic substances in the sample. Urine was decolorized under UV irradiation in the presence
of hydrogen peroxide. As a result, color quenching was considerably suppressed and higher counting efficiency of tritium was
obtained. This UV treatment made it possible to increase the urine content in the sample from 2 to 40% (v/v) without significant
decrease of counting efficiency. Either higher sensitivity or shorter analysis time was achieved in the tritium measurement
by the augmentation of urine content. When the measurement time was 30 min, the detection limit of tritium defined as 3s was 0.03 Bq/ml. At the expense of some sensitivity (set at a detection limit of 0.3 Bq/ml), the measurement time was shortened
to 0.5 min. These results will make a great improvement to routine tritium monitoring as well as to emergency monitoring in
mass tritium exposure.
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The regularized Newton method (RNM) is one of the efficient solution methods for the unconstrained convex optimization. It
is well-known that the RNM has good convergence properties as compared to the steepest descent method and the pure Newton’s
method. For example, Li, Fukushima, Qi and Yamashita showed that the RNM has a quadratic rate of convergence under the local
error bound condition. Recently, Polyak showed that the global complexity bound of the RNM, which is the first iteration k such that ‖∇f(xk)‖≤ε, is O(ε−4), where f is the objective function and ε is a given positive constant. In this paper, we consider a RNM extended to the unconstrained “nonconvex” optimization. We
show that the extended RNM (E-RNM) has the following properties. (a) The E-RNM has a global convergence property under appropriate
conditions. (b) The global complexity bound of the E-RNM is O(ε−2) if ∇2f is Lipschitz continuous on a certain compact set. (c) The E-RNM has a superlinear rate of convergence under the local error
bound condition. 相似文献
Tetraphenylporphine zinc(II) (ZnTPP) was found to be adsorbed from its CH2Cl2 solution into a Nafion (Nf) film. The characteristics of the adsorption of ZnTPP into the Nf film were studied using a visible absorption spectroscopic technique. The initial rate (v0, mol cm(-2) s(-1)) for uptake of ZnTPP was saturated with increasing ZnTPP concentration (c0, M) in the solution. This kinetic profile was analyzed in terms of a Michaelis-Menten model considering preequilibrium of ZnTPP adsorption between the solution and the outer layer of the Nf film, followed by diffusion to an inner bulk region, giving a maximum diffusion reflux of v(max) = (2.2 +/- 0.2) x 10(-13) mol cm(-2) s(-1). This is different from the kinetics for the Nf/phthalocyanine zinc(II) (ZnPc) film, which gives a linear plot of v(0) vs c(0). This can be explained by the relatively slow diffusion of ZnTPP in the film compared to that of ZnPc because of steric factors: ZnTPP contains bulky tetraphenyl moieties attached perpendicular to a porphyrin ring, whereas ZnPc has higher planarity. The isotherm for the adsorption of ZnTPP into the Nf film was analyzed using a Langmuir isotherm equation, yielding an equilibrium constant of (3.6 +/- 1.1) x 10(6) M(-1) and a saturated amount of adsorbed ZnTPP of (1.8 +/- 0.1) x 10(-9) mol cm(-2), suggesting monolayer adsorption of ZnTPP on the hydrophobic polymer network interfacial with hydrophilic transport channels without significant intermolecular overlap. This is in contrast to the multilayer adsorption mode suggested for the ZnPc adsorption. The tetraphenyl moieties could prevent the stacking of ZnTPP for multilayer adsorption. 相似文献
The polycondensation reaction of 3,4‐ethylenedioxythiophene with 2,7‐dibromo‐9,9‐dioctylfluorene via Pd‐catalyzed direct arylation gives poly[(3,4‐ethylenedioxythiophene‐2,5‐diyl)‐(9,9‐dioctylfluorene‐2,7‐diyl)]. The reaction conditions are optimized in terms of the Pd precatalysts, reaction time, and carboxylic acid additives. The combination of 1 mol% Pd(OAc)2 and 1‐adamantanecarboxylic acid as an additive is the optimized catalytic system, and it yields the corresponding polymer with a molecular weight of 39 400 in 89% yield. The polycondensation reaction, followed by an end‐capping reaction, effectively provides a linear polymer without Br terminals. 相似文献
Polycondensation of 1‐(2‐pyrimidinyl)pyrrole with 2,7‐dibromo‐9,9‐dioctylfluorene via Ru‐catalyzed direct arylation gives the corresponding conjugated polymer with a molecular weight of 19 800 in 86% yield. The introduction of directing group, 2‐pyrimidinyl substituent, into the pyrrole monomer induces ortho‐metalation and provides the site‐selective direct arylation polycondensation at the α‐position of pyrrole unit without the protection of β‐position. The removal of 2‐pyrimidinyl substituent on the pyrrole unit proceeds efficiently and results in the enhancement of coplanarity along the main chain of the polymer.
Abstract We study ground state phase diagrams for the MMX chains, using a one-dimensional dimerized 3/4-filled extended Hubbard-Peierls model with site diagonal and off-diagonal electron-lattice interactions. The ground states are obtained mainly in the Hartree-Fock approximation, and their accuracy is checked by the exact diagonalization of small clusters. We find a new phase in addition to frequently considered phases and compare our results with experimental results. 相似文献
Natural sterols often occur as a heterogeneous mixture of homologs, which had disturbed the progress of steroid research. Development and application of GC methodology overcame this difficulty and enabled us to obtain detailed sterol profiles. Together, fine synthesis of stereo-defined isomers and homologs of steroids having oxygenated side chains allowed us to compare them with natural samples as well as to investigate structure-activity relationship. Advance of HPLC technology also facilitated the determination of the stereochemical structure of naturally occurring steroidal compounds, which were obtained only in minute amounts. This review highlights three topics out of our steroid research that have been performed mainly at Tokyo Institute of Technology around 1970–1990. These are sterol metabolism in insects focusing on the mechanism of the conversion of plant sterols to cholesterol and ecdysone biosynthesis, the synthesis and biochemical research of active forms of vitamin D3 derivatives, and the synthesis and microanalysis of plant hormone brassinosteroids. 相似文献
Abstract We have determined the magnetic structure of a low-carrier Kondo-lattice system CeAs, and have observed a softening of the crystalline electric field excitations. Despite the prediction of a recent magnetic polaron model in which CeAs and CeP are expected to show a stacking order of T7 and T8 layers, CeAs does not show such a stacking structure under pressure. The ordering in the intermediate phase is a regular ferromagnetic order and that of the low-temperature phase is a canted type-I AF. 相似文献
The aim of this work was to study the effects of sound frequency, sound intensity and viscosity of slag on the slag foaming rate and the steady-state foam height. Experiments were carried out using two slags (BaO–B2O3) melted at a temperature of 1223 or 1273 K, as well as water–glycerin solutions at room temperature. Low frequency sound waves (<1.3 kHz) are found to be more effective in the slag foaming suppression than high frequency waves (1.3–12 kHz). The steady-state foam height decreases abruptly when the sound pressure reaches a threshold value that depends on sound frequency and liquid viscosity. The results can be explained in terms of enhancing the rates of liquid drainage and film rupture induced by sound. 相似文献