Novel UWB Transceiver for WBAN Networks: A Study on AWGN Channels

A novel ultra‐wideband (UWB) transceiver structure is presented to be used in wireless body area networks (WBANs). In the proposed structure, a data channel and a control channel are combined into a single transmission signal. In the signal, a modulation method mixing pulse position modulation and pulse amplitude modulation is proposed. A mathematical framework calculating the power spectrum density of the proposed pulse‐based signal evaluates its coexistence with conventional radio systems. The transceiver structure is discussed, and the receiving performance is investigated in the additive white Gaussian noise channel. It is demonstrated that the proposed scheme is easier to match to the UWB emission mask than conventional UWB systems. The proposed scheme achieves the data rate requirement of WBAN; the logical control channel achieves better receiving performance than the logical data channel, which is useful for controlling and maintaining networks. The proposed scheme is also easy to implement.     

A Low‐Complexity 128‐Point Mixed‐Radix FFT Processor for MB‐OFDM UWB Systems

In this paper, we present a fast Fourier transform (FFT) processor with four parallel data paths for multiband orthogonal frequency‐division multiplexing ultra‐wideband systems. The proposed 128‐point FFT processor employs both a modified radix‐2⁴ algorithm and a radix‐2³ algorithm to significantly reduce the numbers of complex constant multipliers and complex booth multipliers. It also employs substructure‐sharing multiplication units instead of constant multipliers to efficiently conduct multiplication operations with only addition and shift operations. The proposed FFT processor is implemented and tested using 0.18 µm CMOS technology with a supply voltage of 1.8 V. The hardware‐ efficient 128‐point FFT processor with four data streams can support a data processing rate of up to 1 Gsample/s while consuming 112 mW. The implementation results show that the proposed 128‐point mixed‐radix FFT architecture significantly reduces the hardware cost and power consumption in comparison to existing 128‐point FFT architectures.     

Direction finding receiver for UWB impulse radio signal in multipath environment

In this paper, we propose a direction finding (DF) receiver for ultra wideband impulse radio (UWB‐IR) signal in a realistic multipath environment. The receiver uses an array of antenna, where each antenna is connected to a proposed propagation‐delay estimation structure. The advantage of the proposed structure is that it outputs a trapezoidal signal whose amplitude reflects the propagation delay and thus relaxes the sampling rate requirement of the analog‐to‐digital‐converter (ADC). The angle‐of‐arrival (AOA) is estimated from the vector of propagation delays measured with respect to reference antenna. Because these estimated delays contain outliers, we propose a simple AOA estimation algorithm based on minimum fractional‐distance search. Experimental results based on simulation show that the proposed DF receiver achieves better performance compared with the minimum ?₁‐ and ?₂‐based (least‐squares based) distance search. Copyright © 2010 John Wiley & Sons, Ltd.     

Sulfonated polyether sulfone‐poly(vinylidene fluoride) blend membrane for DMFC applications

Direct methanol fuel cell (DMFC) proton exchange membranes were prepared by blending poly (vinylidene fluoride) (PVDF) with sulfonated poly(ether sulfone) (SPES). Using a diffusion cell and gas chromatographic technique, the effects of PVDF content on methanol permeability in the blended membranes were investigated. The thermal resistance and proton conductivity of the membranes were also determined by using a thermal gravimetric analysis (TGA) and an impedance analysis technique respectively. The presence of sulfonic acid groups in SPES was confirmed by Fourier transform infrared (FTIR). It was found that the methanol permeability in the blended membranes decreased with PVDF content at the expense of proton conductivity. Blended membranes show methanol permeability values much lower than that of Nafion 115, whereas the proton conductivities of the membranes are comparable with that of Nafion. The thermal stability of these blended membranes is above 250°C, which is sufficiently high for use in DMFC. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Crossflow filtration of iron(III), copper(II), and cadmium(II) aqueous solutions with alginic acid/cellulose composite membranes

The removal of Fe(III), Cu(II), and Cd(II) ions from aqueous solutions was investigated with a crossflow filtration technique. Alginic acid (AA)/cellulose composite membranes were used for retention. In the filtration of Fe(III) solutions, the effects of the crossflow velocity, applied pressure, AA content of the membranes, and pH on the retention percentage and the permeate flux were examined. The maximum retention percentage was found to be 89% for a 1 × 10^?4M Fe(III) solution at the flow velocity of 100 mL/min and the pressure of 60 kPa with 0.50% (w/v) AA/cellulose composite membranes at pH 3. Aqueous solutions of Cu(II) and Cd(II) were filtered at the flow velocity of 100 mL/min and pressure of 10 kPa. The effects of the AA content of the membranes and pH of the waste medium on the retention percentage and the permeate flux were determined. For 1 × 10^?4M Cu(II) and Cd(II) solutions, the maximum retention percentages were found to be 94 and 75%, respectively, at pH 7 with 0.50% (w/v) AA/cellulose composite membranes. When metal‐ion mixtures were used, the retention percentages of Fe(III), Cu(II), and Cd(II) were found to be 89, 48, and 10%, respectively, at pH 3 with 0.50% (w/v) AA/cellulose composite membranes. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Effect of the particle size and particle agglomeration on composite membrane performance

One of the most used methods for studying the rigidification of polymer matrices in composite membranes is differential scanning calorimetry. Glass‐transition temperatures give information about filler–polymer interaction and the rigidity of the polymer matrix. In this study, optical microscopy, mechanical property testing, and X‐ray diffraction, instead of differential scanning calorimetry, were used to study both poly(ether imide) (PEI) matrix rigidification and activated carbon–PEI interfacial adhesion. Then, the permselective properties of the mixed matrix membranes were interpreted. The change in rigidity in these composite membranes was in agreement with the decrease in the flexibility of the composite materials as the filler content increased. This fact was confirmed by the tension and elongation data and X‐ray diffraction (DRX) measurements. However, the Young's modulus value decreased as the carbon content increased. There was an increase in all of the gas permeability coefficients measured in the composites compared with that of PEI. As the particle size grew, a low particle surface area and a poor interfacial adhesion were observed. The carbon agglomerates acted as sites of stress concentration within the polymeric matrix. This decreased the intercatenary distances and limited the movement of polymer chains, which resulted in a more rigid matrix. The higher selectivity of the H₂/CH₄, H₂/CO₂ and O₂/N₂ systems observed in the composite membranes revealed that there were both a preferential sorption of certain gases in the carbon surface or carbon–polymer interface and a molecular size exclusion, which were responsible for that increment, despite the poor interfacial adhesion. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Structure and gas permeation properties of asymmetric polyimide membranes made by dry–wet phase inversion: Influence of the polyimide molecular weight

In this article, we report the influence of the polyimide molecular weight (1.2 × 10⁵, 2.6 × 10⁵, and 4.1 × 10⁵) on the structure and the gas permeation properties of asymmetric polyimide membranes made by the dry–wet phase‐inversion process. The apparent skin layer thickness of the asymmetric membrane increased with increasing molecular weight, and the thicknesses of the membranes prepared from the three polyimides with a casting polymer solution containing 8.0 wt % butanol were 132, 350, and 739 nm, respectively. That is, the gas permeance in the asymmetric membranes increased with decreasing molecular weight. In contrast, the gas selectivity of the asymmetric membranes did not depend on the skin layer thickness. The solvent evaporation in the dry phase‐inversion process and the nonsolvent diffusion in the dry process were important factors that determined the formation of the asymmetric membrane. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Asymmetric cellulose acetate dialysis membranes: Synthesis,characterization, and performance

Cellulose acetate (CA) is highly comparable to other synthetic polymer materials and is effective in the hemodialysis process. In this work, asymmetric CA membranes were synthesized with the phase‐inversion method. CA with a molecular weight of 52,000, poly(ethylene glycol) (PEG) with a molecular weight of 400, and 1‐methyl‐2‐pyrrolidone (NMP) were used as the polymer, additive, and solvent, respectively. The effects of the CA and PEG concentrations and coagulation bath temperature (CBT) on the morphology, pure water permeability (PWP), insulin/human serum albumin (HSA) transmission, and finally thermal and chemical stability of the prepared membranes were determined and investigated. In general, increasing the PEG concentration and CBT and reducing the CA concentration resulted in increased PWP and insulin/HSA transmission. Also, these variations facilitated the formation of macrovoids in the membrane sublayer. On the other hand, increasing the PEG and CA concentrations and reducing CBT resulted in increased thermal and chemical stability of the prepared membranes. Also, ratios of 15.5/10/74.5 and 17.5/10/72.5 (w/w) for the CA/PEG/NMP casting solutions and their immersion into coagulation baths with CBTs of 0 and 25°C, respectively, resulted in the preparation of membranes that had not only optimum sieving properties and higher PWP but also thermal and chemical stability better than that of conventional CA hemodialysis membranes. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Nitrophenoxy groups containing polybenzimidazoles as polymer electrolytes for fuel cells: Synthesis and characterization

Polybenzimidazoles containing different contents of pendant nitrophenoxy groups were prepared by condensation of 3,3′‐diamino‐benzidine with a mixture of 3,5‐dicarboxyl‐4′‐nitro diphenyl ether and isophthalic acid (IPA) in different ratios in polyphosphoric acid. The polymers are soluble in polar aprotic solvents, they have inherent viscosities in the range of 0.75–1.10 dL g^?1 and they form tough and transparent films on solution casting. They have good thermal stability with initial decomposition temperature ranging from 380 to 416°C in nitrogen, good tensile strength ranging from 56 to 65 MPa and reasonably good oxidative stability. Phosphoric acid uptake of these polymers is low compared with PBI and membranes doped with phosphoric acid exhibit good proton conductivity in the range of 6.6× 10^?3 to 1.9× 10^?2 S/cm at 25°C and 1.2× 10^?2 to 4.9× 10^?2 S/cm at 175°C, compared with 3.9× 10^?3 S/cm at 25°C and 3.2× 10^?2 S/cm at 175°C for PBI. These membranes are suitable for applications as polymer electrolyte for fuel cell and presumably for gas separation at high temperature. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

低温烧成高纯Al_2O_3多孔陶瓷膜支撑体的制备

为了降低高纯Al2O3(α-Al2O3质量含量≥99%)多孔陶瓷膜支撑体烧成温度,以粒径为30μm的α-Al2O3为原料,分别添加TiO2和TiO2/Cu(NO3)2为烧结助剂,通过干压成型和挤出成型制备片状和管式多孔支撑体。Al2O3-TiO2和Al2O3-TiO2-CuO体系分别在高温下出现的液相低共熔物促进了多孔支撑体的烧结。当氧化铝支撑体中添加0.5%(摩尔分数,下同)TiO2+0.5%Cu(NO3)2后,在1600℃的烧成即可获得机械性能高、渗透性能好和耐酸碱腐蚀性能优异的管式支撑体。在压力为0.1MPa时,支撑体的水渗透通量为12.1m3/(m2·h),弯曲强度为44.5MPa。经过80℃,含10%(质量分数,下同)HNO3的溶液腐蚀800h及80℃,含10%NaOH的溶液1200h后,支撑体的质量损失率分别为1%和0.35%。