High-pressure studies on Tc and crystal structure of iron chalcogenide superconductors

The superconducting transition temperature, T_c, in iron-based solids can be enhanced by applied pressure: T_c increases from 8 to 37 K for the 11-type FeSe when the pressure is raised from 0 to 4 GPa. High-pressure studies can elucidate the mechanism of superconductivity in such novel materials. In this paper, we present a high-pressure study of Fe(Se_1−xTe_x) and Fe(Se_1−xS_x). In the case of Fe(Se_1−xTe_x), the maximum T_c under high pressure did not exceed the T_c of FeSe, which can be attributed to the structural transition to the monoclinic phase. For Fe(Se_1−xS_x) (0 < x < 0.3), T_c exhibited a significant increase with pressure; however, the maximum T_c under high pressure did not exceed the T_c of FeSe. This may be due to the disorder induced by substituting S for Se, which is similar to the pressure effect on T_c for the 1111-type superconductor Ca(Fe_1−xCo_x)AsF. The T_c of Fe(Se_1−xS_x) showed a complex behavior below 1 GPa, first decreasing and then increasing with increasing pressure. From high-pressure x-ray diffraction measurements, the T_c (P) curve was correlated with the local structural parameter.     

Catalytic decomposition of HCFC22 (CHClF2)

The catalytic decomposition of CHClF₂ was studied over various acidic metal oxides in a fixed-bed reactor. The Cr₂O₃ZrO₂ exhibited the highest activity. The presence of water vapor in the reaction system suppresses the transformation of oxides to fluorides, progresses the formation of CO₂, and it improves the catalysts life.     

Synthesis of 4‐Aryl‐2‐Quinolones via Copper‐Catalyzed Hydroarylation of (o‐Aminophenyl)propiolates with Arylboronates

4‐Aryl‐2(1H)‐quinolones were efficiently synthesized via copper‐catalyzed hydroarylation of (o‐aminophenyl)propiolates with arylboronic acid neopentyl glycol esters. The substrate propiolates were prepared from the corresponding silylalkynes with carbon dioxide by Kondo’s carboxylation method using N,N‐dimethylformamide as a solvent. Hydroarylation was performed in the presence of 3 mol% copper(II) acetate in methanol at 28 °C for 12 h and subsequent deprotection using trifluoromethanesulfonic acid (3.0 equiv.) at 65 °C for 2 h in the same pot to afford the desired 4‐aryl‐2(1H)‐quinolones in 39–89% yields.

     

The mathematical model for the formaldehyde emission from wood-based board in room

A mathematical model which describes the influence of various parameters on formaldehyde concentration in the atmosphere of a room containing wood-based boards was developed. The physical meanings and measuring methods of the parameters of the model are also discussed. Based on this model, two indices for commenting the formaldehyde emission process of wood-based boards are proposed, and inequality estimation for the formaldehyde content of wood-based boards at any moment and a time estimation which shows when the room satisfies the environment quality standard are also given.     

Influence of Particle Size on the Distributions of Liposomes to Atherosclerotic Lesions in Mice

ABSTRACT

In order to confirm the efficacy of liposomes as a drug carrier for atherosclerotic therapy, the influence of particle size on the distribution of liposomes to atherosclerotic lesions in mice was investigated. In brief, liposomes of three different particle sizes (500, 200, and 70 nm) were prepared, and the uptake of liposomes by the macrophages and foam cells in vitro and the biodistributions of liposomes administered intravenously to atherogenic mice in vivo were examined. The uptake by the macrophages and foam cells increased with the increase in particle size. Although the elimination rate from the blood circulation and the hepatic and splenic distribution increased with the increase in particle size in atherogenic mice, the aortic distribution was independent of the particle size. The aortic distribution of 200 nm liposomes was the highest in comparison with the other sizes. Surprisingly, the aortic distribution of liposomes in vivo did not correspond with the uptake by macrophages and foam cells in vitro. These results suggest that there is an optimal size for the distribution of liposomes to atherosclerotic lesions.     

Nondestructive Quantitative Evaluation of Porosity Volume Distribution in Aluminum Alloy Die Castings by Fractal Analysis

The nondestructive and three-dimensional quantitative evaluation of porosity in aluminum alloy die castings is proposed to identify whether the predominant cause of pore formation is shrinkage or entrapped gas. The validity of this method of evaluation was shown by comparing two different regions with different ratios of pores formed by shrinkage and gas. It was shown that the proposed evaluation can be used as a quantitative indication of porosity.     

Overall Adsorption Isotherm of Natural Organic Matter

Adsorption equilibrium data in lumped water quality indices obtained for diluted solutions of a peat water and effluents from a wastewater treatment were analyzed using the ideal adsorbed solution theory with the Freundlich equation. The use of the same value for Freundlich exponent 1∕n in the ideal adsorbed solution theory resulted in a straightforward and less computationally demanding expression to describe an overall batch adsorption isotherm. A fictive component approach, assuming a logarithmic normal distribution of Freundlich K and a nonadsorbable fraction, adequately described and predicted the overall isotherms for different initial concentrations of diluted solutions presented as a lumped water quality index. The parameters in the distributed fictive component approach were independently sensitive to each portion of an isotherm curvature. Preferential adsorption of the smaller molecular weight (MW) components was observed by a size-exclusion high-performance liquid chromatography. Two-dimensional distribution analysis of organics in terms of Freundlich K and MW revealed a weak tendency of the adsorptive strength to decrease with the increase of the MW.     

The separation of fission-product rare elements toward bridging the nuclear and soft energy systems

Based on the present state of the art of the separation technology, recycling of fission-product rare elements (FRE) in the FBR spent fuel is discussed. The rad.-waste fractionation is in accordance with the present society's trend toward zero-emission, and the mean of salt-free method utilizing electrochemistry agrees with the principles of the newly established green chemistry. A catalytic electrolytic extraction method is proposed to separate the target, radioactive but potentially strategic elements, Pd, Ru, Rh, Re (Tc), Te and Se dissolved in the HLLW. It avoids secondary waste arising. This method is particularly feasible for the separation of Pd where cyclic reaction of metal cations such as Pd(II) or Fe(II), acting as promoters or mediators and already contained in HLLW, accelerates the electrochemical deposition of Ru, Rh and Re. Elemental separation not only offers alternative material resources to meet expanding demands for catalysts in Fuel Cell/Soft Energy system but is also the first step for transmutation or other selective strategies for waste management of long-lived fission products (LLFP).