A Sulfur–Limonene‐Based Electrode for Lithium–Sulfur Batteries: High‐Performance by Self‐Protection

The lithium–sulfur battery is considered as one of the most promising energy storage systems and has received enormous attentions due to its high energy density and low cost. However, polysulfide dissolution and the resulting shuttle effects hinder its practical application unless very costly solutions are considered. Herein, a sulfur‐rich polymer termed sulfur–limonene polysulfide is proposed as powerful electroactive material that uniquely combines decisive advantages and leads out of this dilemma. It is amenable to a large‐scale synthesis by the abundant, inexpensive, and environmentally benign raw materials sulfur and limonene (from orange and lemon peels). Moreover, owing to self‐protection and confinement of lithium sulfide and sulfur, detrimental dissolution and shuttle effects are successfully avoided. The sulfur–limonene‐based electrodes (without elaborate synthesis or surface modification) exhibit excellent electrochemical performances characterized by high discharge capacities (≈1000 mA h g^?1 at C/2) and remarkable cycle stability (average fading rate as low as 0.008% per cycle during 300 cycles).     

Human experience and product usability: principles to assist the design of user-product interactions

This paper introduces research that investigates how human experience influences people's understandings of product usability. It describes an experiment that employs visual representation of concepts to elicit participants' ideas of a product's use. Results from the experiment lead to the identification of relationships between human experience, knowledge, and context-of-use - relationships that influence designers' and users' concepts of product usability. These relationships are translated into design principles that inform the design activity with respect to the aspects of experience that trigger people's understanding of a product's use. A design tool (ECEDT) is devised to aid designers in the application of these principles. This tool is then trialled in the context of a design task in order to verify applicability of the findings.     

An integral method for measuring the <Emphasis Type="Italic">P</Emphasis>-odd asymmetry on a reactor at neutron polarization switching frequencies higher than the frequencies of the main spectrum of the neutron noise power

P-odd asymmetry is measured when frequencies of switching neutron polarization exceed the frequencies of the reactor power fluctuations that govern the spectral density of noise power. A principle for recording the current signals in these measurements is described. This method was used for the first time at the Konstantinov Institute of Nuclear Physics in Gatchina (Russia). The results suggest that the accuracy of measurements at an increased equipment-switching frequency is even higher than the accuracy obtained using compensation for reactor power fluctuations; hence, this compensation becomes superfluous. Following this method, it is possible to take measurements with a single detector and to dispense with a monitor, thereby rendering the equipment and the measuring technique less complex. A strategy of measurements was developed. An experimental model of the facility was produced and tested with a small-amplitude calibration signal in the presence of reactor power fluctuations caused by rays from reaction ¹⁰B(n )⁷ Li* ⁷Li + . The results from the test measurements of the P-odd effect in reaction ³⁵Cl(n, )³⁶Cl are presented.Translated from Pribory i Tekhnika Eksperimenta, No. 1, 2005, pp. 62–71.Original Russian Text Copyright ¢ 2004 by Vesna, Shulgina.     

Second order derivative spectrophotometric method for determination of vitamin C content in fruits,vegetables and fruit juices

A second-order derivative UV spectrophotometric method for determination of vitamin C [ascorbic acid (AA)] content in a variety of natural samples is described. The method is based on the measurement of a peak–baseline amplitude in the second derivative of the AA spectrum at 267.5 nm. The following corresponding regression equation was obtained within the concentration range 2×10^-5 to 1×10^-4 M AA (3.5–17.6 g/cm³ AA) in 1.0 M HCl solution: ²D_267.5=2.420×10⁴ c+0.025; the correlation coefficient was 0.9993 and the detection limit 4.2×10^-6 M. The results obtained by analysing 21 different species of fruits, vegetables and juices indicated a possibility for a more extensive application of the proposed method. This method is rapid, simple and requires no pretreatment of the analysed material, which makes it suitable for routine analyses. The reliability of the method was confirmed by comparative determinations with the generally accepted 2,6-dichloroindophenol method.     

Kinetics of struvite to newberyite transformation in the precipitation system MgCl2-NH4H2PO4NaOH-H2O

The influence of the initial reactant concentrations on the composition of the solid phases formed in the precipitation system MgCl(2)-NH(4)H(2)PO(4)-NaOH-H(2)O was investigated. The precipitation diagram constructed shows the approximate concentration regions within which struvite, newberyite, and their mixtures exist at 25 degrees C and an aging time of 60 min. It was found that immediately after mixing the reactant solutions, struvite (MgNH(4)PO(4).6H(2)O) precipitated in nearly the whole concentration area, while newberyite (MgHPO(4).3H(2)O) appeared mostly within the region of the excess of magnesium concentration. It was also found that after aging time of 60 min the precipitation domain of struvite alone is much broader than that of newberyite or the domain of their coexistence, and shows that struvite is more abundant in the systems in which the initial concentration of ammonium phosphate is higher than that of magnesium. The kinetics of struvite to newberyite transformation (conversion) was systematically studied under the conditions of different initial reactant concentrations and different initial pH in the systems in which a mixture of both phases precipitated spontaneously. The struvite to newberyite conversion period was found to be strongly related to the ratio of initial supersaturations, S(N)/S(S), rather than to the any particular physical quantity that can describe and predict the behavior of the precipitation system. Experimental data suggest a solution-mediated process as a most possible transformation mechanism. Along with a continuous monitoring of the changes in the liquid phase, the content of struvite in the solid phase was estimated by means of a Fourier transform infrared (FT-IR) method, developed for this particular precipitation system.