|
| ||
|
|
||
Cell Configuration (cell + configuration)
Selected AbstractsBroadband wireless access based on VSF-OFCDM and VSCRF-CDMA and its experimentsEUROPEAN TRANSACTIONS ON TELECOMMUNICATIONS, Issue 3 2004Hiroyuki Atarashi This paper presents broadband packet wireless access schemes based on variable spreading factor (VSF)-orthogonal frequency and code division multiplexing (OFCDM) in the downlink and variable spreading and chip repetition factors (VSCRF)-CDMA in the uplink for the systems beyond IMT-2000. In our design concept for wireless access in both links, radio parameters such as the spreading factor (SF) are optimally controlled so that the system capacity is maximized according to the cell configuration, channel load and radio channel conditions, based on the tradeoff between efficient suppression of other-cell interference and the capacity increase in the target cell by exploiting orthogonality in the time and frequency domains. We demonstrate that the peak throughput of greater than 100,Mbps and 20,Mbps is achieved by the implemented base station and mobile station transceivers using the 100-MHz and 40-MHz bandwidths in the downlink and uplink respectively. Moreover, the simulation results show the possibility of the peak throughput of approximately 1,Gbps for short-range area applications using the 100-MHz bandwidth OFCDM downlink by applying four-branch multiple input multiple output (MIMO) multiplexing with 16,QAM data modulation and punctured turbo coding. Copyright © 2004 AEI [source] Application of Electrochemical Impedance Spectroscopy for Fuel Cell Characterization: PEFC and Oxygen Reduction Reaction in Alkaline Solution,FUEL CELLS, Issue 3 2009N. Wagner Abstract The most common method used to characterise the electrochemical performance of fuel cells is the recording of current/voltage U(i) curves. Separation of electrochemical and ohmic contributions to the U(i) characteristics requires additional experimental techniques like electrochemical impedance spectroscopy (EIS). The application of EIS is an approach to determine parameters which have proved to be indispensable for the characterisation and development of all types of fuel cell electrodes and electrolyte electrode assemblies [1]. In addition to EIS semi-empirical approaches based on simplified mathematical models can be used to fit experimental U(i) curves [2]. By varying the operating conditions of the fuel cell and by the simulation of the measured EIS with an appropriate equivalent circuit, it is possible to split the cell impedance into electrode impedances and electrolyte resistance. Integration in the current density domain of the individual impedance elements enables the calculation of the individual overpotentials in the fuel cell (PEFC) and the assignment of voltage loss to the different processes. In case of using a three electrode cell configuration with a reference electrode, one can directly determine the corresponding overvoltage. For the evaluation of the measured impedance spectra the porous electrode model of Göhr [3] was used. This porous electrode model includes different impedance contributions like impedance of the interface porous layer/pore, interface porous layer/electrolyte, interface porous layer/bulk, impedance of the porous layer and impedance of the pores filled by electrolyte. [source] Limitations of amorphous content quantification by isothermal calorimetry using saturated salt solutions to control relative humidity: Alternative methodsJOURNAL OF PHARMACEUTICAL SCIENCES, Issue 4 2010Nawel Khalef Abstract Despite the high sensitivity of isothermal calorimetry (IC), reported measurements of amorphous content by this technique show significant variability even for the same compound. An investigation into the reasons behind such variability is presented using amorphous lactose and salbutamol sulfate as model compounds. An analysis was carried out on the heat evolved as a result of the exchange of water vapor between the solid sample during crystallization and the saline solution reservoir. The use of saturated salt solutions as means of control of the vapor pressure of water within sealed ampoules bears inherent limitations that lead in turn to the variability associated with the IC technique. We present an alternative IC method, based on an open cell configuration that effectively addresses the limitations encountered with the sealed ampoule system. The proposed approach yields an integral whose value is proportional to the amorphous content in the sample, thus enabling reliable and consistent quantifications. © 2009 Wiley-Liss, Inc. and the American Pharmacists Association J Pharm Sci 99: 2080,2089, 2010 [source] Regulation by FK506 and rapamycin of Ca2+ release from the sarcoplasmic reticulum in vascular smooth muscle: the role of FK506 binding proteins and mTORBRITISH JOURNAL OF PHARMACOLOGY, Issue 4 2009D MacMillan Background and purpose:, The sarcoplasmic reticulum (SR), regulates the cytoplasmic Ca2+ concentration ([Ca2+]cyto) in vascular smooth muscle. Release from the SR is controlled by two intracellular receptor/channel complexes, the ryanodine receptor (RyR) and the inositol 1,4,5-trisphosphate receptor (IP3R). These receptors may be regulated by the accessory FK506-binding protein (FKBP) either directly, by binding to the channel, or indirectly via FKBP modulation of two targets, the phosphatase, calcineurin or the kinase, mammalian target of rapamycin (mTOR). Experimental approach:, Single portal vein myocytes were voltage-clamped in whole cell configuration and [Ca2+]cyto measured using fluo-3. IP3Rs were activated by photolysis of caged IP3 and RyRs activated by hydrostatic application of caffeine. Key results:, FK506 which displaces FKBP from each receptor (to inhibit calcineurin) increased the [Ca2+]cyto rise evoked by activation of either RyR or IP3R. Rapamycin which displaces FKBP (to inhibit mTOR) also increased the amplitude of the caffeine-evoked, but reduced the IP3 -evoked [Ca2+]cyto rise. None of the phosphatase inhibitors, cypermethrin, okadaic acid or calcineurin inhibitory peptide, altered either caffeine- or IP3 -evoked [Ca2+]cyto release; calcineurin did not contribute to FK506-mediated potentiation of RyR- or IP3R-mediated Ca2+ release. The mTOR inhibitor LY294002, like rapamycin, decreased IP3 -evoked Ca2+ release. Conclusions and implications:, Ca2+ release in portal vein myocytes, via RyR, was modulated directly by FKBP binding to the channel; neither calcineurin nor mTOR contributed to this regulation. However, IP3R-mediated Ca2+ release, while also modulated directly by FKBP may be additionally regulated by mTOR. Rapamycin inhibition of IP3 -mediated Ca2+ release may be explained by mTOR inhibition. [source] Redox Cycling of Ni-Based Solid Oxide Fuel Cell Anodes: A ReviewFUEL CELLS, Issue 3 2007D. Sarantaridis Abstract The published literature relating to damage to SOFCs caused by redox cycling of Ni-based anodes is reviewed. The review covers the kinetics of Ni oxidation and NiO reduction (as single phases and as constituents of composites with yttria-stabilised zirconia, YSZ), the dimensional changes associated with redox cycling and the effect of this on the mechanical integrity and electrical performance of cells and stacks. A critical parameter is the expansion strain that is caused by oxidation. Several studies report that the first complete oxidation of a Ni/YSZ composite causes a linear expansion of the order of 1%, but the actual values vary substantially between different investigations. The oxidation strain is the result of microstructural irreversibility during the redox process and leads to strain accumulation over several redox cycles. This can cause mechanical disruption to an anode, anode support or other cell components attached to the anode. A simplified mechanical model of the stress and damage that are likely to be caused by anode expansion is proposed and applied to anode-supported, electrolyte-supported and inert substrate-supported cell configurations. This allows the maximum oxidation strain to avoid damage in each configuration to be estimated. [source] | ||||||||||