A universal dependence for thermal conductivity of metals and dilute alloys

A universal curve relating the maximum of thermal conductivity and its respective temperature with the residual electrical resistivity has been proposed for metals and dilute alloys. Based on the equation of that curve, a comparative analysis of selected literature data of thermal conductivity of metals, which have residual electrical resistivity in the range 10^–11<₀<10^–5. cm, have been performed. Using the data for 33 metals, confirmation of the Wiedemann-Franz law for the impurity component/T of thermal conductivity was obtained, which means that _th/_el1, where _th and _el are the parameters of the electron-lattice defect interaction obtained from measurements of thermal and electrical conductivity, respectively. Examples of the failure of the Wiedemann-Franz law are also presented, exhibiting the values of _th/_el in the range 0.16 to 25. Measurements of thermal conductivity in the range 2 to 20 K and determination of the residual electrical resistivity for the samples of Cd doped with Zn and quenched were performed, resulting in values _th/_el1.     

Influence of Nb5+ ions on phase transitions and polar disorder above TC in PbZrO3 studied by Raman spectroscopy

Micro-Raman light scattering experiments on PbZrO₃ (PZO) single crystal doped with Nb⁵⁺ have been investigated. Special attention was paid to the paraelectric (PE) phase in which nominally forbidden first-order Raman spectra were detected at temperatures far above the phase transition T_C. Complex Raman spectra were observed in the vicinity of three structural phase transitions. These results mainly from the coexistence of phases with different symmetries in a wide temperature range below T_C. The Raman measurements have been compared with dielectric and optical observations and proved that polar nanoregions in a centrosymmetric lattice appear well above T_C. It was shown that doping ABO₃ perovskites with heterovalent ions like Nb⁵⁺ unbalances charge neutrality of the lattice and strongly extends the temperature range of polar regions. The investigations performed point out that in the PE matrix the interaction between electrons and lattice vibrations, as recently suggested for pure PZO, plays an important role.     

The influence of brewing method on bioactive compounds residues in spent coffee grounds of different roasting degree and geographical origin

The content of bioactive compounds in spent coffee grounds (SGC) was studied. SGC were obtained from Coffea arabica beans of different roasting degrees (light and dark) and different geographical origins (Nicaragua, Columbia and Mexico) processed using four brewing methods (mocha, filtered, drip and infusion). The highest caffeine and chlorogenic acid contents were determined in filtered spent coffee extracts. All extracts of light roasted spent coffee grounds showed lower browning index levels in comparison to that from dark roasted spent coffee grounds. Generally, the highest content of total polyphenolic compounds and highest antioxidant capacity were determined in extracts prepared in drip. In conclusion, the results obtained in this study indicate that the spent coffee grounds produced of domestic levels, especially those obtained from filter coffeemaker, could be considered as a good source of natural antioxidants.     

Iron(II) Sulfate(VI) from Titania Production as a Raw Material for Preparation of Hydrogen Sulfide Sorbents

A hybrid sorbent material for removal of hydrogen sulfide from air was developed. The material is based on activated carbon and iron compounds obtained from waste iron(II) sulfate(VI) heptahydrate. The iron salt is deposited on the carbonaceous support and subjected to oxidation (Fe²⁺ to Fe³⁺) using atmospheric oxygen under alkaline conditions. An effect of H₂O₂ addition to the process on the composition of the resultant material was also examined. X-ray diffraction (XRD) analyses confirmed easy conversion of waste FeSO₄·7H₂O to iron oxides Fe₃O₄ and FeOOH. The activated carbon supporting iron oxides revealed a higher efficiency in H₂S elimination from air compared to the commercial activated carbon, without any modification.     

Multiscale approach to the morphology,structure, and segmental dynamics of complex degradable aliphatic polyurethanes

A multiscale approach spanning from the segmental (subnanometer) up to micrometer level was applied for detailed study of the self‐assembly of aliphatic block polyurethane (PU) elastomers. To understand the principles of the self‐organization of hard and soft segments in the complex multi‐component systems, several two‐component model PU samples, that is, the products of 1,6‐diisocyanatohexane (HDI) with three diols differing in the length and constitution were also prepared, characterized, and investigated: (i) polycarbonate‐based macrodiol (MD), (ii) biodegradable oligomeric diol (DL‐L; product of butane‐1,4‐diol and D,L‐lactide), and (iii) butane‐1,4‐diol (BD). The study (particularly ¹³C‐¹H PILGRIM NMR spectra) reveals complex internal organization and interesting (application appealing) behavior of multi‐component PUs. Hard segments (HDI+BD products) feature self‐assembled and significantly folded chain conformations with interdomain spacing 15–22 nm (small‐angle X‐ray scattering analysis). The small domains are hierarchically assembled in various structural formations of µm size (spherulites) depending on PU composition, as detected by transmission electron microscopy and atomic force microscopy. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41590.     

Limitations of the potential step technique to impedance measurements using discrete time Fourier transform

Recently, a new method of measuring impedance of electrochemical systems was proposed in the literature by Yoo and Park (Yoo, J.-S.; Park, S.-M. Anal. Chem. 2000, 72, 2035). It is based on the analysis of system response to a potential step. Differentiation of the applied potential step and the current response in the time domain followed by applying Fourier transform to both signals allows for determination of the system's impedance. It has been proposed that the measurements carried out in a short time period permit the determination of the system's impedance in the whole frequency range. The aim of the present work was to verify the validity of the impedance spectra obtained using this method, as well as to establish the conditions for which the method may be used. This method was tested using simulated data for a simple ideally polarized electrode and a simple one-electron redox system in the solution. The results show that the reliable impedance spectra may be obtained only for frequencies between 1/(NDeltat) and 1/(2Deltat), where Deltat denotes the sampling time and N is the number of points acquired during the experiment. However, the artifacts are generated when the experimental data are extrapolated to lower frequencies.     

Enhancement of solid dissolution process under the influence of rotating magnetic field

The main objective of this work is to study the effect of rotating magnetic field (RMF) on the dissolution process of NaCl-cylindrical sample. The experimental investigations are provided for the explanation of the influence on the dissolution process of a solid body to surrounding its dilute solution in the experimental set-up with the RMF generator. The analysis indicated the strong influence of the localization NaCl-cylindrical sample on the enhancement of mass transfer process. The mass transfer process under the action of RMF is described by means of the dimensionless equation with the local magnetic Taylor number.     

Effect of metal purity and testing procedure on surface tension measurements of liquid tin

The surface tension of liquid tin of three different grades of purity (99.85, 99.96, and 99.999%) was measured by the classical sessile drop method over the temperature range 523–1023 K, in heating and cooling regimes. The results obtained show that the metal purity affects the values of surface tension and its temperature dependence. The highest values of surface tension and smooth linear temperature dependence were obtained in cooling regime for tin of the highest purity. With increasing content of impurities, both surface tension and its temperature coefficient decrease while the scatter of the data increases. The surface tension values measured on heating regime show higher scatter, compared to those obtained in cooling regime, and the temperature dependence of the surface tension is curvilinear rather than linear.