Improvement in the DOA estimation of broadband signals usingpartially IIR beamformers

An ideal broadband beamformer requires an increased number of taps for each filter, which in turn increases the complexity of the design. It is shown that for angles near the broadside of the antenna the beamforming is more accurate compared to the angles near the endfire, and it is advantageous to use recursive filters combined with a computed number of zeros for angles near the endfire. The proposed method is used for estimating the arrival angle of the incoming signals and displays uniform accuracy for all angles     

A Novel UWB Pulse Shape Modulation System

In this paper novel modified Hermite polynomial functions for use in impulse radio (ultra-wideband) communications are proposed. With these functions pulse shapes which are orthogonal and have nearly constant pulse width regardless of the pulse order are generated. These properties hold under the effects of differentiation. An M-ary communication system is constructed using these pulse shapes. A Matlab model for generating the pulses is designed and the effect of timing jitter on the performance of the system is investigated by computer simulation.     

Facile synthesis of polyoxometalate-based composite with doped ternary NiCoFe cations as electrocatalyst for oxygen evolution reaction

The construction of efficient and low-cost electrocatalysts for oxygen evolution reactions (OER) to replace precious catalysts is a necessity to achieve economic production of hydrogen. Herein, we report an efficient tri-metallic electrocatalysts for the OER that is prepared by incorporate nickel, cobalt and iron cations on Triton X-100/phosphotungstic acid organic-inorganic composite without utilize any binders or energy consumer procedure. Considering to the synergy effect of simultaneous absorption of NiCoFe cations on composite substrate, the as-made tri-metallic catalyst exhibits excellent OER activity with a small overpotential of 210 and 330 mV at a current density of 10 and 100 mA cm^?2, respectively. Moreover, remarkable trends in electrocatalytic activity of mono-, bi- and tri-metallic electrocatalysts at low (10 mA) and high (100 mA) current density are observed. In addition, this new families of non-precious metal catalyst shows long-term durability in 1 M KOH.     

Room temperature oxidation of acetone by ozone over alumina-supported manganese and cobalt mixed oxides

Volatile organic compounds (VOCs) are among the major sources of air pollution. Catalytic ozonation is an efficient process for removing VOCs at lower reaction temperature compared to catalytic oxidation. In this study, a series of alumina supported single and mixed manganese and cobalt oxides catalysts were used for ozonation of acetone at room temperature. The influence of augmenting the single Mn and Co catalysts were investigated on the performance and structure of the catalyst. The manganese and cobalt single and mixed oxides catalysts of the formula Mn10%-CoX and Co10%-MnX (where X= 0, 2.5%, 5%, or 10%) were prepared. It was found that addition of Mn and Co at lower loading levels (2.5% or 5%) to single metal oxide catalysts enhanced the catalytic activity. The mixed oxides catalysts of (Mn10%-Co2.5%) and (Mn10%-Co5%) led to acetone conversion of about 84%. It is concluded that lower oxidation state of the secondary metal improves ozone decomposition and oxidation of acetone.     

Photocatalytic degradation of Direct Red 23 dye using UV/TiO2: Effect of operational parameters

In this study, the photocatalytic degradation of Direct Red 23 (Scarlet F-4BS) was investigated in UV/TiO2 system. The effect of catalyst loading and pH on the reaction rate was ascertained and optimum conditions for maximum degradation were determined. The results obtained showed that acidic pH is proper for the photocatalytic removal of Direct Red 23. In addition, the effects of several cations (Cu2+, Al3+, Cr3+, and Sn4+) and anions (BiO3(-), SO4(2-), and CN(-)) and C2H5OH were examined in this photocatalytic process. On the order hand, three types of catalysts (Fe2O3, SnO2, and ZnO) were compared with TiO2. After 90 min reaction, the relative decomposition order established was UV/TiO2>UV/SnO2>UV/Fe2O3>UV/ZnO.     

Effects of mercaptopropionic acid as a stabilizing agent and Cd:Te ion ratio on CdTe and CdHgTe quantum dots properties

In the present work, mercaptopropionic acid (MPA) capped CdTe and CdHgTe quantum dots (QDs) are synthesized using a method based on the bottom up approach in aqueous medium. The CdTe QDs were prepared with a two different ratios of Cd:Te (3:1 and 4:1). It was noticed that there was a minimum concentration of MPA for each Cd:Te ratio. The resulting QDs were characterized using optical absorption spectroscopy, energy dispersion X-ray (EDX) and high resolution transmission electron microscopy (HRTEM). It was found that the EDXs of CdTe and CdHgTe QDs showed that the stiochiometric ratios of CdTe obtained with Cd:Te ratio of 3:1 is 50:50 and for CdHgTe is 40:26:34 for 100?% of Hg. The band gap of CdHgTe QDs varies slightly with composition from 2.21?eV for a pure CdTe to 1.4?eV for a CdHgTe with 100?% of Hg. The HRTEM image showed a good dispersed nano-crystalline structure for the CdTe QDs with average size of 3–4?nm. The existence of the lattice planes on the HRTEM images of the QD indicated that the CdTe QDs are highly crystalline. In addition, the CdHgTe QDs size is 12?nm for 100?% of Hg.     

Poly(o-aminophenol) film prepared in the presence of sodium dodecyl sulfate: Application for nickel ion dispersion and the electrocatalytic oxidation of methanol and ethylene glycol

Poly(o-aminophenol) (POAP) was formed by successive cyclic voltammetry in monomer solution in the presence of sodium dodecyl sulfate (SDS) on the surface of a carbon paste electrode. The electrochemical behavior of the SDS-POAP carbon paste electrode has been investigated by cyclic voltammetry in 0.5 M HClO₄ and 5 mM K₄[Fe(CN)₆]/0.1 M KCl solutions as the supporting electrolyte and model system, respectively. Ni(II) ions were incorporated into the electrode by immersion of the polymeric modified electrode having amine groups in 0.1 M Ni(II) ion solution. Cyclic voltammetric and chronoamperometric experiments were used for the electrochemical study of this modified electrode. A good redox behavior of the Ni(III)/Ni(II) couple at the surface of electrode can be observed. The electrocatalytic oxidations of methanol and ethylene glycol (EG) at the surface of the Ni/SDS-POAP electrode were studied in a 0.1 M NaOH solution. Compared to bare carbon paste and POAP-modified carbon paste electrodes, the SDS-POAP electrode significantly enhanced the catalytic efficiency of Ni ions for methanol oxidation. Finally, using a chronoamperometric method, the catalytic rate constants (k) for methanol and ethylene glycol were found to be 2.04 × 10⁵ and 1.05 × 10⁷ cm³ mol⁻¹ s⁻¹, respectively.     

Comparison between wavelet-based and Fourier-based multicarrier UWB systems

The use of wavelet transform in multicarrier ultra wideband (UWB) systems is analysed and the results are compared with Fourier-based multicarrier UWB systems. It is well known that convolution in time domain is equivalent to multiplication in frequency domain; however, there is no closed-form expression in the literature for convolution's counterpart in the wavelet domain. A formula is derived to represent convolution's counterpart in the wavelet domain. Furthermore, the effects of choice and type of wavelet filters and different decomposition levels are investigated. Finally, a performance comparison of both techniques for IEEE 802.15.3a channel models using IEEE802.15.3a multiband-orthogonal frequency division multiplexing UWB specifications is provided.