(Pr0.9La0.1)2(Ni0.74Cu0.21Ga0.05)O4+δ-Ce0.9Gd0.1O2-δ复合阴极的制备及电化学性质

采用EDTA-柠檬酸盐法制备了(Pr0.9La0.1)2(Ni0.74Cu0.21Ga0.05)O4+δ(PLNCG),并与Ce0.9Gd0.1O2-δ(CGO)形成复合阴极PLNCG-CGO。XRD和SEM分析结果表明PLNCG与CGO在1 000℃具有较好的化学相容性。电化学阻抗测试结果表明PLNCG-30%CGO复合阴极在700℃的极化电阻为0.092Ω·cm2;过电位为39.3 m V时,电流密度达到113.3 m A·cm-2。氧分压分析表明电极反应的速率控制步骤为电荷转移过程。阳极支撑单电池(Ni-CGO/CGO/PLNCG-30%CGO)在700℃的最大输出功率密度达到569 m W·cm-2,开路电压(OCV)为0.76 V。     

Mn-Al和Cu-Mn-Al复合氧化物催化苯甲醇选择氧化反应

用溶胶-凝胶法制备了不同组成的Mn-Al和Cu-Mn-Al复合氧化物两组催化剂,用于苯甲醇选择氧化反应.用X射线衍射(XRD)、N2物理吸附(BET)、扫描电镜(SEM)、H_2程序升温还原(H_2-TPR)、O_2程序升温脱附(O_2-TPD)和X射线光电子能谱(XPS)技术对催化剂进行了结构表征,考察了催化剂组成对催化活性的影响.结果表明:以甲苯为溶剂,O_2为氧化剂,353 K反应5 h,Mn_2Al和Cu_(0.3)Mn_(0.7)Al_2催化剂上的苯甲醇转化率分别为36.6%和40.9%,苯甲醛选择性均为100%.进一步研究表明:催化剂活性与其H2还原性和O_2吸附性有关,高活性的催化剂吸附氧多,生成的活性氧易参与反应.     

High strength cellulose composite films reinforced with clay for applications as antibacterial materials

High strength cellulose composite films with antibacterial activities were prepared by dispersing montmorillonites (MMT) into cellulose solution in LiOH/urea aqueous solvent followed by regeneration in ethanol coagulation bath, and then by soaking in 5 wt% hexadecylpyridine bromide ethanol solutions to induce the antibacterial action. The cellulose/MMT composite films were characterized by field emission scanning electron microscopy, transmission electron microscopy, thermogravimetric analysis, FTIR, UV-spectra, wide angle X-ray diffraction and mechanical test. The results revealed that MMT was dispersed well in the cellulose matrix to form layer structure with a thickness of approximately 3 nm. The mechanical properties of the cellulose/MMT composite films were significantly improved to achieve 132 MP for tensile strength as a result of the MMT delamination. The hexadecylpyridine bromide was fixed well in the cellulose/MMT matrix through cation exchange, leading to the excellent antibacterial activities against Staphylococcus aureus and Escherichia coli, which is important in their practical applications.     

Electrochemical sensors for the simultaneous determination of zinc,cadmium and lead using a Nafion/ionic liquid/graphene composite modified screen-printed carbon electrode

A simple, low cost, and highly sensitive electrochemical sensor, based on a Nafion/ionic liquid/graphene composite modified screen-printed carbon electrode (N/IL/G/SPCE) was developed to determine zinc (Zn(II)), cadmium (Cd(II)), and lead (Pb(II)) simultaneously. This disposable electrode shows excellent conductivity and fast electron transfer kinetics. By in situ plating with a bismuth film (BiF), the developed electrode exhibited well-defined and separate peaks for Zn(II), Cd(II), and Pb(II) by square wave anodic stripping voltammetry (SWASV). Analytical characteristics of the BiF/N/IL/G/SPCE were explored with calibration curves which were found to be linear for Zn(II), Cd(II), and Pb(II) concentrations over the range from 0.1 to 100.0 ng L⁻¹. With an accumulation period of 120 s detection limits of 0.09 ng mL⁻¹, 0.06 ng L⁻¹ and 0.08 ng L⁻¹ were obtained for Zn(II), Cd(II) and Pb(II), respectively using the BiF/N/IL/G/SPCE sensor, calculated as 3σ value of the blank. In addition, the developed electrode displayed a good repeatability and reproducibility. The interference from other common ions associated with Zn(II), Cd(II) and Pb(II) detection could be effectively avoided. Finally, the proposed analytical procedure was applied to detect the trace metal ions in drinking water samples with satisfactory results which demonstrates the suitability of the BiF/N/IL/G/SPCE to detect heavy metals in water samples and the results agreed well with those obtained by inductively coupled plasma mass spectrometry.     

还原氧化石墨烯/Au复合微电极阵列的制备及光电特性

利用双光束干涉-无掩模光刻技术制备了周期性氧化石墨烯微结构阵列,利用肼蒸气对氧化石墨烯脱氧还原,然后蒸镀超薄Au薄膜制备了还原氧化石墨烯/Au复合微电极阵列(R-GO/Au).对复合电极在可见光波段的透过率和表面电阻进行了表征,结果表明,R-GO/Au复合微电极阵列具有良好的光电特性.将R-GO/Au复合微电极阵列引入到有机太阳电池中作为半透明阳极,器件的光电转化效率可达3.43%.     

Preparation of magnetic nanoparticles by the use of self-assembled fluorinated oligomeric aggregates—A new approach to the dispersion of magnetic particles on poly(methyl methacrylate) film surface

Fluoroalkyl end-capped acrylic acid oligomer-encapsulated magnetic nanoparticles were prepared by the coprecipitation of aqueous ferric and ferrous ions in the presence of the corresponding oligomers under alkaline conditions. The dynamic light scattering measurements showed that these fluorinated oligomer magnetic nanoparticles were encapsulated in the self-assemblies of fluoroalkyl end-capped oligomers. Fluoroalkyl end-capped oligomer-encapsulated magnetic nanoparticles thus obtained were applied to the dispersion of magnetic particles on the poly(methyl methacrylate) film surface to exhibit not only the surface active property imparted by fluorine but also magnetic behavior toward a permanent magnet.     

Sequential Voltammetric Determination of Uranium,Cadmium and Lead by Using the ex situ Bismuth Film Electrode: Application to Phosphate Fertilizers

A sequential voltammetric procedure for the determination of uranium, cadmium and lead was investigated at an ex situ bismuth film electrode (BiFE). First, the adsorptive stripping voltammetry was applied to assay the U(VI)‐cupferron complex in the differential pulse mode (detection limit of 1.0 µg L^?1, 200 s accumulation time). Through the manipulation of the same aliquot of the sample, efforts were made to quantify cadmium and lead by square wave anodic stripping voltammetry. Detection limits of 2.03 µg L^?1 for Cd (II) and 2.43 µg L^?1 for Pb (II) were calculated (100 s accumulation time). The methodology was successfully applied to phosphate fertilizer samples after open vessel wet decomposition (HNO₃/H₂O₂). The following value ranges were evaluated: U (VI) 37.2–150 mg kg^?1, Pb (II) 78.3–204 mg kg^?1 and Cd (II) 44.1–71.6 mg kg^?1. Validation was performed by using the standard reference materials SRM‐695 – phosphate fertilizer – and SRM‐1643e – water.     

Corrosion resistances of passive films on low‐Cr steel and carbon steel in simulated concrete pore solution

The passive ranges of carbon steel rebar and 3Cr steel rebar in saturated Ca(OH)₂‐simulated concrete pore solution with pH 12.6 were determined by means of cyclic voltammetry and potentiodynamic polarization curves. Chronopotentiometry was used to obtain steady‐state conditions for the formation of passive films on rebar samples at different anodic potentials. Electrochemical impedance spectroscopy, Mott–Schottky and X‐ray photoelectron spectrometer curves were employed to compare the formed passive films at different potentials. Additionally, cyclic polarization curves were used to compare the corrosion resistances of formed passive films on the two rebars in saturated Ca(OH)₂‐simulated concrete pore solution with different concentration of Cl^?. The results show that the passive ranges of the two rebars are all between ?0.15 and +0.6 V, and more stable passive films can be formed on both rebars at the anodic potential of +0.3 V. In the absence of Cl^?, the stability and corrosion resistance of the passive film formed on the 3Cr rebar are better than those of CS rebar. The passive film of 3Cr steel has the relatively better pitting corrosion resistance than carbon steel in saturated Ca(OH)₂‐simulated concrete pore solution that contains different concentration of Cl^?. Copyright © 2016 John Wiley & Sons, Ltd.     

Characterization of N-cyclohexylmethacrylamide LB thin films for room temperature vapor sensor application

This study reports the synthesis, characterization and gas sensing applications of N-cyclohexylmethacrylamide (NCMA) monomer material using FT-IR, ¹H and ¹³C NMR, UV-visible spectroscopy, Quartz Crystal Microbalance (QCM) and Langmuir-Blodgett (LB) thin film deposition techniques. The thin film deposition conditions of NCMA monomer material, which are prepared by LB film technique, are characterized by UV-visible spectroscopy and QCM system. The sensing behaviors of the LB film with respect to volatile organic compounds (VOCs) at room temperature are investigated. Surface pressure change as a function of surface area of NCMA molecule at the water surface shows a well-organized and stable monolayer at 18 mN m^?1 surface pressure value for LB film deposition. Transfer ratio values are found to be ≥ 0.94 for quartz glass and ≥ 0.93 for quartz crystal substrate. The typical frequency shift per layer is obtained 20.10 Hz/layer and the deposited mass onto a quartz crystal is calculated as 824.62 ng/layer. The sensing responses of the LB films against chloroform, dichloromethane, acetone, toluene, benzene and ethanol are measured by QCM system. The sensitivities of the NCMA LB film sensor are determined between 0.085 and 0.029 Hz ppm^?1. Sensitivities with detection limits are between 35.29 and 100.33 ppm against organic vapors. These results can be concluded that the monomer LB film sample is found to be significantly more sensitive to chloroform and dichloromethane vapors than others organic vapors used in this work. This material may find potential applications in the development of room temperature organic vapor sensing.     

Viscoelastic response and interlaminar delamination resistance of epoxy/glass fiber/functionalized graphene oxide multi-scale composites

Graphene oxide (GO) was functionalized using three different diamines, namely ethylenediamine (EDA), 4,4′-diaminodiphenyl sulfone (DDS) and p-phenylenediamine (PPD) to reinforce an epoxy/glass fiber (EP/GF) composite laminate, with the aim of improving the overall composite mechanical performance. Different mechanical characterization techniques were used to determine the mechanical performance, including: tensile stress strain, double cantilever beam (DCB) mode-I fracture toughness and dynamic mechanical thermal analysis (DMTA). Scanning electron microscopy (SEM) was used to support the results and conclusions. The results demonstrated remarkable enhancements in the mechanical performance of EP/GF composite laminates by incorporation of functionalized graphene oxide (FGO) nanofiller, whilst the mechanical performance of the GO reinforced composite only improved marginally. Finally, the mechanical performance of the EP/GF/FGO multi-scale composites was found to be dependent on the type of FGO functional groups; of which EDA exhibited the highest performance. These investigations confirmed that the EDA-FGO-reinforced EP/GF composites possess excellent potential to be used as multifunctional engineering materials in industrial applications.