Wireless Power Transmission for Power Supply: State of Art

The wireless power supply is motivated by simple and comfortable use of many small electric appliances with low power input. This paper reviews the concepts which are suitable for wireless power transmission with respect to power supply of such appliances in small areas. The categorization of the concepts is made. The efficiency of the concepts is discussed on general base. The reference levels for exposure to electric and magnetic fields are mentioned, and maximal power delivered to an appliance by fulfillment of these levels is considered

Vapour reactive distillation process for hydrogen production by hi decomposition from hi-i2-h2o solutions

In this contribution, a sequential and hierarchical approach for the feasibility analysis and the preliminary design of reactive distillation columns is extended to systems involving vapour phase chemical reaction and is successfully applied to the HI vapour phase decomposition to produce H2. The complex phase and physico chemical behaviour of the quaternary HI-H2-I2-H2O system is represented by the Neumann’s thermodynamic model and instantaneous vapour phase chemical equilibrium is assumed. Then, from minimal information concerning the physicochemical properties of the system, three successive steps lead to the design of the unit and the specification of its operating conditions: the feasibility analysis, the synthesis and the design step. First, the analysis of reactive condensation curve map method (rCCM), assuming infinite internal liquid and vapour flow rate and infinite reflux ratio, is used to assess the feasibility of the process. It determines the column structure and estimates the attainable compositions. These results are used as inputs data for the synthesis step. Based on the boundary value design method (BVD), considering finite internal liquid and vapour flow rate and finite reflux ratio while neglecting all thermal effects and assuming a constant heat of vaporisation, the synthesis step provides more precise information about the process configuration (minimum reflux ratio, number of theoretical stages, localisation and number of reactive plates, position of the feed plate). Finally, the BVD method results are used to initialise rigorous simulations, based on an equilibrium stage model with energy balance, to estimate the reflux ratio taking into account thermal effect on the process. The resulting design configuration consists in a single feed and entirely reactive distillation column. The column operates under a pressure of 22 bars. The feed of the reactive distillation column, coming from the Bunsen reaction section [xHI=0.10; xI2=0.39 xH2O=0.51], is at its boiling temperature. The residue consists in pure iodine. Water and produced hydrogen are recovered at the distillate. The column operates at a reflux ratio of 5 and is composed of 11 theoretical plates including the reboiler and the partial condenser with the feed at the stage 10 (counted downwards). The obtained HI dissociation yield is 99.6%

Wireless power transmission: R&D activities within Europe

Wireless power transmission (WPT) is an emerging technology that is gaining increased visibility in recent years. Efficient WPT circuits, systems and strategies can address a large group of applications spanning from batteryless systems, battery-free sensors, passive RF identification, near-field communications, and many others. WPT is a fundamental enabling technology of the Internet of Things concept, as well as machine-to-machine communications, since it minimizes the use of batteries and eliminates wired power connections. WPT technology brings together RF and dc circuit and system designers with different backgrounds on circuit design, novel materials and applications, and regulatory issues, forming a cross disciplinary team in order to achieve an efficient transmission of power over the air interface. This paper aims to present WPT technology in an integrated way, addressing state-of-the-art and challenges, and to discuss future R&D perspectives summarizing recent activities in Europe.The work of N. Borges Carvalho and A. J. S. Soares Boaventura was supported by the Portuguese Foundation for Science and Technology (FCT) under Project CREATION EXCL/EEI-TEL/0067/2012 and Doctoral Scholarship SFRH/BD/80615/2011. The work of H. Rogier was supported by BELSPO through the IAP Phase VII BESTCOM project and the Fund for Scientific Research-Flanders (FWO-V). The work of A. Georgiadis and A. Collado was supported by the European Union (EU) under Marie Curie FP7-PEOPLE-2009-IAPP 251557 and the Spanish Ministry of Economy and Competitiveness Project TEC 2012-39143. The work of J. A. García and M. N. Ruíz was supported by the Spanish Ministries MICINN and MINECO under FEDER co-funded Project TEC2011-29126-C03-01 and Project CSD2008-00068. The work of J. Kracek and M. Mazanek was supported in part by the Czech Ministry of Education Youth and Sports under Project OC09075–Novel Emerging Wireless Systems

Deliquescence of NaCl–NaNO(3), KNO(3)–NaNO(3), and NaCl–KNO(3 )salt mixtures from 90 to 120°C

We conducted reversed deliquescence experiments in saturated NaCl–NaNO(3)–H(2)O, KNO(3)–NaNO(3)–H(2)O, and NaCl–KNO(3)–H(2)O systems from 90 to 120°C as a function of relative humidity and solution composition. NaCl, NaNO(3), and KNO(3 )represent members of dust salt assemblages that are likely to deliquesce and form concentrated brines on high-level radioactive waste package surfaces in a repository environment at Yucca Mountain, NV. Discrepancy between model prediction and experiment can be as high as 8% for relative humidity and 50% for dissolved ion concentration. The discrepancy is attributed primarily to the use of 25°C models for Cl–NO(3 )and K–NO(3 )ion interactions in the current Yucca Mountain Project high-temperature Pitzer model to describe the nonideal behavior of these highly concentrated solutions

Evaporative sodium salt crust development and its wind tunnel derived transport dynamics under variable climatic conditions

Playas (or ephemeral lakes) can be significant sources of dust, but they are typically covered by salt crusts of variable mineralogy and these introduce uncertainty into dust emission predictions. Despite the importance of crust mineralogy to emission potential, little is known about (i) the effect of short-term changes in temperature and relative humidity on the erodibility of these crusts, and (ii) the influence of crust degradation and mineralogy on wind speed threshold for dust emission. Our understanding of systems where emission is not driven by impacts from saltators is particularly poor. This paper describes a wind tunnel study in which dust emission in the absence of saltating particles was measured for a suite of climatic conditions and salt crust types commonly found on Sua Pan, Botswana. The crusts were found to be non-emissive under climate conditions characteristic of dawn and early morning, as compared to hot and dry daytime conditions when the wind speed threshold for dust emission appears to be highly variable, depending upon salt crust physicochemistry. Significantly, sodium sulphate rich crusts were found to be more emissive than crusts formed from sodium chloride, while degraded versions of both crusts had a lower emission threshold than fresh, continuous crusts. The results from this study are in agreement with in-situ field measurements and confirm that dust emission from salt crusted surfaces can occur without saltation, although the vertical fluxes are orders of magnitude lower (∼10 μg/m/s) than for aeolian systems where entrainment is driven by particle impact

Silver(I) sulfide: Ag2S Heat capacity from 5 to 1000 K, thermodynamic properties, and transitions

The heat capacity of Ag2S has been measured by adiabatic-shield calorimetry from 5 to 1000 K. The heat capacity increases regularly up to about 445 K where the pre-transitional contribution causes rapidly rising values. The [alpha]-to-[beta] transition of Ag2S occurs in the range 449.3 to 451.3 K, depending upon previous history of the sample. The enthalpy of transition [Delta]trsHm = (4058+/-26) J[middle dot]mol-1. A slightly decreasing heat capacity is observed for [beta]-Ag2S from 88.1 J[middle dot]K-1[middle dot]mol-1 at 460 K to 85.0 J[middle dot]K-1[middle dot]mol-1 at 850 K with a minimum of 84.6 J[middle dot]K-1[middle dot]mol-1 at 750 K. The transition of [beta]-Ag2S to [gamma]-Ag2S occurs at about 865 K with [Delta]trsHm = (784+/-5) J[middle dot]mol-1. Thermodynamic functions have been evaluated and the values of Cp,m, "Smo(T)-Smo(0)', and -"Gmo(T)-Hmo(0)'/T at 298.15 K are 75.31, 142.89, 85.43, and at 1000 K are 80.57, 253.28, 172.77 J[middle dot]K-1[middle dot]mol-1, respectively. No signs of further transitions were found, either in the stoichiometric compound, or in a sample with overall composition Ag2S1.0526. Thus, the present work does not support the hypothesis of Perrott and Fletcher concerning partial disordering of stoichiometric Ag2S around 600 K as opposed to complete disordering around 450 K in the presence of excess silver or sulfur. Subtraction of the estimated lattice heat capacity at constant pressure leaves a large transitional heat capacity for [beta]-Ag2S above 450 K. It is about 11 J[middle dot]K-1[middle dot]mol-1 at 500 K and decreases gradually to about 6 J[middle dot]K-1[middle dot]mol-1 at 850 K. Its origin is discussed.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/26409/1/0000496.pd