Positron study of the martensitic transformation in Fe-29.5at.%Ni

Precision measurements of positron lifetime spectra in Fe-29.5at.%Ni alloy specimens were performed to clarify the nature of the martensitic transformation in this alloy. The forward transformation did not introduce any defects which behave as strong trapping sites for positrons. On the other hand, the reverse transformation accompanied the production of defects, to which the positron lifetime is sensitive, maybe dislocations. From the present results, the nature of the transformation was discussed.     

Horseradish peroxidase-catalyzed polymerization of<Emphasis Type="Italic"> p</Emphasis>-hydroxycinnamic acid for synthesis of reactive microspheres

In this article, we report the experimental synthesis of reactive polymer microspheres of poly(p-hydroxycinnamic acid). Enzyme-catalyzed polymerization of poly(p-hydroxycinnamic acid) using horseradish peroxidase as a catalyst and hydrogen peroxide as an oxidant took place in a mixture solution of methanol and phosphate buffer solution; it was found that the fraction of methanol in the mixture solution strongly affected the yield of powdery polymer materials. The chemical structure of the polymers was characterized by ¹H-NMR and FT-IR spectroscopies, and the molecular weight was measured by gel permeation chromatography. The ¹H-NMR chart of the obtained polymer was almost the same as that of the monomer; FT-IR spectra indicated the existence of carboxyl groups. The weight-average molecular weight of the soluble part in tetrahydrofuran was found to be 1,451. Dispersion polymerization of p-hydroxycinnamic acid was carried out in a mixture solution of methanol and phosphate buffer solution by adding a dispersion stabilizer. Of the several such polymers tested, poly(vinyl alcohol) was found to be the most effective in producing reactive poly(p-hydroxycinnamic acid) microspheres.     

An experimental trial for the determination of the critical coagulation concentration using the sedimentation method

A method for determining the critical coagulation concentration (C _c) from the change in the transmittance of the sol with stand time after adding a coagulating agent is discussed. Potassium nitrate was used as the coagulating agent because the specific adsorption of electrolyte ions on the particle and the hydrolysis of electrolyte ions are negligible. Apparent critical coagulation concentrations,C _c ^a, of iron (III) hydroxide and silver iodide sols were obtained from the transmittance vs. potassium nitrate concentration curves for various stand times. The values ofC _c ^a decreased with increasing stand time. TheC _c ^a value obtained for the shortest stand time was closer toC _c obtained from the initial turbidity change of the sol by applying Rayleigh's law. The Hamaker constant for the particle in water was calculated from theC _c ^a value obtained at the shortest time and the experimentally determined outer Helmholtz plane potential. The calculated Hamaker constants were comparable to the theoretical values for iron (III) hydroxide and silver iodide.     

Initial crystallization mechanism of isotactic polystyrene from different States

The isothermal crystallization processes of isotactic polystyrene at 160 degrees C from different initial states (quenched glassy state and melt state), i.e., cold- and melt-crystallization processes, have been investigated by infrared (IR) and generalized two-dimensional (2D) IR correlation spectroscopy. It has been found that not only the crystallization kinetics and crystallinity but also the sequential changes of the amorphous and crystalline sensitive bands are quite different for the cold- and melt-crystallization processes. This leads to the conclusion that the physical origins for spinodal decomposition prior to polymer crystallization may be different for different crystallization processes.     

Dietary,but not topical,alpha-linolenic acid suppresses UVB-induced skin injury in hairless mice when compared with linoleic acids

Peroxidizability of fatty acids in the air is roughly proportional to the number of double bonds, but in vivo peroxidation proceeds in a more complex manner. Here, we compared the effects of dietary and topically applied oils enriched with linoleic acid (LA, 18:2n-6) or alpha-linolenic acid (ALA, 18:3n-3) on UV-induced skin injury in a strain of hairless mice. The UVB-induced erythema score was significantly lower in mice with topically applied creams containing LA and ALA than in mice with the basal cream; no significant increase in the score was detected in the ALA group compared with the LA group. However, dietary ALA inhibited the increase in erythema score after UVB irradiation compared with LA. The peroxidizability index of the skin total lipids was significantly higher, but UVB-induced prostaglandin E2 (PGE2) production was significantly lower in the group fed an ALA-rich diet compared with the group fed an LA-rich diet. The levels of thiobarbituric acid-reactive substances, estimated in the presence of butylated hydroxytoluene in the assay mixture, were not affected by UVB treatment or by the dietary fatty acids, but the severity of the skin lesion was associated with PGE2 levels. These results indicate that the type of fatty acids, n-6 or n-3, is critical for the suppression of UVB-induced skin lesion when the skin fatty acids are modified by dietary manipulation. Anti-inflammatory activity of dietary flaxseed oil with relatively high ALA and low LA contents was demonstrated in UVB-irradiated hairless mice.     

A new method for the synthesis of novel 6-quinoxalinylpyrazolo[5,1-c][1,2,4]triazines

The reaction of the quinoxaline 1 with 4-ethoxycarbonyl-1H-pyrazole-5-diazonium chloride 7 at room temperature gave 3-[α-(4-ethoxycarbonyl-1H-pyrazol-5-ylhydrazono)methoxycarbonylmethyl]-2-oxo-1,2-dihydroquinoxaline 8. The pmr spectrum of 8 in deuteriodimethylsulfoxide supported the presence of two tautomers 8-I and 8-II. Refluxing of 8 in N,N-dimethylformamide or acetic acid resulted in cyclization to afford 8-ethoxycarbonyl-4-oxo-3-(3-oxo-3,4-dihydroquinoxalin-2-yl)-1,4-dihydropyrazolo[5,1-c][1,2,4]triazine 9. Compound 9 was also obtained directly by the reaction of 1 with 7 under reflux in better yield. The reaction of 9 with hydrazine hydrate provided the hydrazinium salt 10 , while the reactions of 9 with triethyl and trimethyl orthoformates in the presence of 1,8-diazabicyclo[5,4,0]-7-undecene produced 8-ethoxycarbonyl-4-ethoxyl-3-(3-oxo-3,4-dihydroquinoxalin-2-yl)pyrazolo[5,1-c][1,2,4]triazine 11a and 8-ethoxycarbonyl-4-methoxyl-3-(3-oxo-3,4-dihydroquinoxalin-2-yl)pyrazolo[5,1-c][1,2,4]triazine 11b , respectively. The chlorination of 11a with phosphoryl chloride gave 3-(3-chloroquinoxalin-2-yl)-8-ethoxycarbonyl-4-ethoxylpyrazolo[5,1-c]-[1,2,4]triazine 12 , whose reaction with morpholine afforded 8-ethoxycarbonyl-4-ethoxyl-3-[3-(morpholin-4-yl)-quinoxalin-2-yl]pyrazolo[5,1-c][1,2,4]triazine 13.     

Tong-type identity and the mean square of the error term for an extended Selberg class

In 1956, Tong established an asymptotic formula for the mean square of the error term of the summatory function of the Piltz divisor function d3(n). The aim of this paper is to generalize Tong's method to a class of Dirichlet series L(s) which satisfies a functional equation. Let a(n) be an arithmetical function related to a Dirichlet series L(s), and let E(x) be the error term of ′n xa(n). In this paper, after introducing a class of Diriclet series with a general functional equation(which contains the well-known Selberg class), we establish a Tong-type identity and a Tong-type truncated formula for the error term of the Riesz mean of the coefficients of this Dirichlet series L(s). This kind of Tong-type truncated formula could be used to study the mean square of E(x) under a certain assumption. In other words, we reduce the mean square of E(x) to the problem of finding a suitable constant σ*which is related to the mean square estimate of L(s). We shall represent some results of functions in the Selberg class of degrees 2–4.     

Calorimetric study on the electronic structure in UP-US system

The heat capacity of UP_1?xS_x (x = 0.0, 0.1, 0.2, 0.4, 0.6, 0.8, 1.0) has been measured from 80 to 670 K by laser-flash calorimetry. All samples exhibit an anomaly corresponding to the magnetic transition. The magnetic transition temperatures determined are in good agreement with literature values. UP_0.4S_0.6 shows an additional small peak at 86 K below T_c. It has been derived that the US-rich ferromagnetically ordered state should be divided into two phases in terms of the direction of the moments. Above 250 K, the heat capacities of all samples increase monotonically with temperature and are well represented in the form of C_p= 6R + AT ? BT^?2. The conduction band structure has been derived from the high-temperature linear term and has been compared with that in literature. It has been suggested that the magnetically ordering behavior such as the direction of the moments would be closely correlated with the band structure.     

Synthesis and characterization of p-phenylenediamine derivatives bearing an electron-acceptor unit

[reaction: see text] Two series of aniline oligomers bearing fused heterocycles as an electron-acceptor unit were synthesized. They consist of aniline or its derivatives as an electron donor and benzothiadiazole (BT) or quinoxaline (QX) as an electron-acceptor unit. Benzothiadiazoles 1-3 were synthesized by palladium-catalyzed amination. Quinoxalines 4-6 were prepared by palladium-catalyzed amination or transformation from the benzothiadiazoles. These compounds showed a HOMO-LUMO gap smaller than those of their analogues such as thiophene-substituted BT/QXs. Cyclic voltammetry revealed that the electrochemical behavior is dependent on the position of the acceptor heterocycle. Chemical oxidation with Ag2O afforded the corresponding 1,4-quinonediimine derivatives as an E,E-isomer, stereoselectively. As for the BT pentamer analogues 2 and 3, the first oxidation selectively occurred at the amino group adjacent to the benzothiadiazole unit, giving the regiospecific half-oxidized derivatives. Furthermore, the fully oxidized derivative 24 was isolated and characterized.