Thermodynamic Properties of Superionic Phase Ag<Subscript>4</Subscript>HgSe<Subscript>2</Subscript>I<Subscript>2</Subscript> Determined by the EMF Method

Triangulation of the Ag-Hg-Se-I system in the vicinity of quaternary phase Ag₄HgSe₂I₂ was performed by differential thermal analysis, X-ray diffraction and electromotive force (EMF) methods. The spatial position of the phase region Ag₄HgSe₂I₂-Se-HgI₂ regarding the figurative point of silver was used to write the chemical reaction of formation of Ag₄HgSe₂I₂. The EMF measurements were carried out by applying an electrochemical cell: (–) C|Ag|Ag₂GeS₃ glass|Ag₄HgSe₂I₂, HgI₂, Se|C (+), where C is graphite and Ag₂GeS₃ glass is the fast purely Ag⁺ ions conducting electrolyte. The linear dependence of the EMF of the electrochemical cell on temperature was used to determine the standard thermodynamic values of Ag₄HgSe₂I₂ for the first time.     

Lignite oxidative desulphurization: notice 3—process technological aspects and application of products

International Journal of Coal Science & Technology - The study reviews the process of oxidative desulphurization of high-sulphur Ukrainian lignite, which was performed by coal treatment using...     

Determination of diffusion coefficients in film systems on the basis of Fe/Cr and Cu/Cr

This paper presents the results of investigation of condensation stimulated (CSD) and thermal stimulated (TSD) diffusion in nanoscale film systems on the basis of Fe/Cr and Cu/Cr by Auger-electron spectroscopy method. The film systems were built in ultrahigh vacuum. Auger spectrum was traced during condensation after each increase in thickness of 0.5-1 nm or during film systems annealing from 300 to 683 K over 5 h. According to experimental data the concentration profiles were built and the effective coefficients of CSD and TSD were computed by several mathematical methods. The efficiency of these techniques in different cases was analyzed. The most accurate results were obtained with Weeple and Gauss error methods that take into account the thickness of the diffusant source.     

Hydrogen storage in Co-and Zn-based metal-organic frameworks at ambient temperature

Hydrogen adsorption properties of some Co-and Zn-based Metal-Organic Framework (MOF) materials were studied at near ambient temperatures. Maximal hydrogen storage capacity of 0.75 wt% was found for a Zn-based material at 175 Bar hydrogen pressure and T = −4 °C. Hydrogen adsorption correlated linearly with BET surface area and strongly depends on temperature. Relatively low structural stability of some MOF's results in framework collapse during degassing and hydrogen adsorption measurements.     

An eigenspace projection clustering method for inexact graph matching

In this paper, we show how inexact graph matching (that is, the correspondence between sets of vertices of pairs of graphs) can be solved using the renormalization of projections of the vertices (as defined in this case by their connectivities) into the joint eigenspace of a pair of graphs and a form of relational clustering. An important feature of this eigenspace renormalization projection clustering (EPC) method is its ability to match graphs with different number of vertices. Shock graph-based shape matching is used to illustrate the model and a more objective method for evaluating the approach using random graphs is explored with encouraging results.     

Gold nanowire array electrode for non-enzymatic voltammetric and amperometric glucose detection

The non-enzymatic voltammetric and amperometric detection of glucose using a gold nanowire array electrode is described. The voltammetric detection of glucose was performed by cyclic and differential-pulse voltammetry. The detection of glucose by partial and direct oxidation of glucose during the anodic and cathodic potential sweeps was shown in cyclic voltammetry. An unusual decrease in overpotential for partial oxidation of glucose on a Au NW array electrode was observed. A linear differential-pulse voltammetric response for partial oxidation of glucose was observed up to a glucose concentration of at least 20 mM with a sensitivity of 41.9 μA mM⁻¹ cm⁻² and detection limit below 30 μM (signal-to-noise ratio of 3) for glucose oxidation at low potentials, where the influence of possible intermediates can be avoided. The amperometric response was also linear up to a glucose concentration of 10 mM with a sensitivity of 309.0 μA mM⁻¹ cm⁻². The wide dynamic range and high sensitivity, selectivity and stability, as well as good biocompatibility of the Au NW electrode make it promising for the fabrication of non-enzymatic glucose sensors.     

A streamlined, cost-effective database approach to manage requirements traceability

Requirements traceability offers many benefits to software projects, and it has been identified as critical for successful development. However, numerous challenges exist in the implementation of traceability in the software engineering industry. Some of these challenges can be overcome through organizational policy and procedure changes, but the lack of cost-effective traceability models and tools remains an open problem. A novel, cost-effective solution for the traceability tool problem is proposed, prototyped, and tested in a case study using an actual software project. Metrics from the case study are presented to demonstrate the viability of the proposed solution for the traceability tool problem. The results show that the proposed method offers significant advantages over implementing traceability manually or using existing commercial traceability approaches.     

Copper electroless plating in weakly alkaline electrolytes using DMAB as a reducing agent for metallization on polymer films

Copper electroless plating at low pH (7–9) using dimethylamine borane complex as a reducing agent is studied electrochemically by linear sweep voltammetry, cyclic voltammetry and chronopotentiometry in full electrolytes. We find that the mixed potential theory is not applicable to the described system. We show that both the working potential and the rate-controlling mechanism are dependent on the pH of the solution. The effects of altering the mechanism on the resulting film conductivity, morphology and adhesion are studied on copper films deposited onto a polyimide (PI) substrate.     

Pulse-reverse electrodeposition for mesoporous metal films: combination of hydrogen evolution assisted deposition and electrochemical dealloying

Hydrogen evolution assisted electrodeposition is a new bottom-up technique allowing the fast and simple synthesis of nanometals. Electrochemical dealloying is a top-down approach with the same purpose. In this work, we show that a combination of these two methods in sequence by pulse-reverse electrodeposition can be used to prepare high-surface-area nanostructured metals. Highly porous adherent platinum is obtained by the deposition of CuPt alloy during the cathodic cycles and the selective dissolution of copper during the anodic cycles. The convection created by the movement of the hydrogen bubbles increases the deposition rate and removes the dissolved copper ions from the diffusion layer, which ensures the deposition of a film with the same stoichiometry throughout the whole process. Due to the relatively high ratio of copper atoms on the surface in the as-deposited layer, it is proposed that the dealloying kinetics is significantly higher than that usually observed during the dealloying process in a model system. The proposed approach has several advantages over other methods, such as a very high growth rate and needlessness of any post-treatment processes. A detailed analysis of the effect of pulse-reverse waveform parameters on the properties of the films is presented. Mesoporous platinum with pores and ligaments having characteristic sizes of less than 10 nm, an equivalent surface area of up to ca. 220 m(2) cm(-3), and a roughness factor of more than 1000 is fabricated.