动物组织复电阻抗谱随离体时间的变化

建立基于四电极法的测量系统,测量了犬和兔部分离体组织的复阻抗谱,观察了部分动物组织复电阻抗谱随离体时间而发生的变化,结果发现,随着动物组织离体时间的延长,其复阻抗谱发生显著变化:1、低频段电阻显著增加;2、复阻抗谱的虚部增加(容性成份增加);3、特征频率降低。结合动物组织离体后发生的组织、细胞水平的变化,我们认为:动物组织复电阻抗谱随离体时间的变化应该与组织细胞内液、细胞外液的离子成份变化相关,同时应该与细胞膜活性相关。

Electrodeposition and corrosion behavior of nanostructured Ni-TiN composite films

The Ni-TiN nanocomposite film was successfully electrodeposited on brass copper substrates.The microstructures of the Ni-TiN nanocomposite film were investigated using scanning electron microscopy（SEM） and transmission electron microscopy（TEM）.Its average grain size was analyzed through X-ray diffraction（XRD）,and its anti-corrosion property was studied through potentiodynamic scanning curves and electrochemical impedance spectroscopy（EIS）.The results show that the morphology of Ni-TiN composite film is sensitively dependent on the electroplating current density,TiN nanoparticle concentration,solution stirring speed,bath temperature and pH value of solution.The average grain size of the optimized nanocomposite film is about 50 nm.Meanwhile,the Ni-TiN nanocomposite films are much more resistant to corrosion than pure Ni coatings.

Role of copper in tarnishing process of silver alloys in sulphide media

Silver and silver alloys usually tarnish,which causes some changes in their aesthetic appearance and electrical properties,due to their exposure to sulphide environments(H2S),and this is a problem in the field of corrosion and conservation of cultural heritage metallic artefacts.In this study,the role of copper content in the tarnishing process of 0.925,0.800 and 0.720 silver alloys in a 0.07 vol.%ammonium sulphide solution for different immersion periods was analyzed by electrochemical impedance spectroscopy(EIS)and scanning electron microscopy(SEM).The polarisation curves showed that the copper content and sulphide increased the corrosion current density and delayed the passivation of silver alloys.The impedance spectra collected at the open circuit potential(OCP)showed a single capacitive,incomplete and depressed loop,indicating that the charge transfer resistance decreased as the copper content increased in the alloys.In contrast,the double-layer capacitance increased as the copper content increased.The SEM-EDS analysis confirmed that the copper-rich phase in the silver alloys was selectively dissolved due to the preference of S to react with Cu,resulting in a localised attack,thus delaying the formation of a passive film.A marked localised attack was observed in alloys with lower copper content.The mechanism for the tarnishing of silver alloys in sulphide media was dependent on the nature of the alloy and the greater affinity of copper for sulphur.The dissolution of Ag and Cu to form corrosion products was proposed as the rate determining step.

Effect of friction stir processing on corrosion of Al-TiB2 based composite in 3.5 wt.% sodium chloride solution

The microstructure and corrosion behavior of as-cast and friction stir processed in-situ Al-TiB2 based composite in 3.5 wt.% sodium chloride solution were investigated. The microstructure was characterized using X-ray diffractometry, scanning electron microscopy and electron backscattered diffraction technique while corrosion behavior was evaluated using linear/cyclic potentiodynamic, electrochemical impedance spectroscopy and ASTM–G67 tests. The composite contains sub-micron TiB2 particles in an aluminum matrix with both blocky and fine clusters of Al3Ti agglomerated around TiB2 and displays a low uniform corrosion rate. It is also resistant to pitting as substantiated by the absence of a positive loop in cyclic potentiodynamic tests. This is due to the non-conductive nature of TiB2 particles and a controlled amount of blocky Al3Ti phase. However, both friction stir processed and as-cast composites are susceptible to inter-granular corrosion where Al3Ti and TiB2 at grain boundaries provide initiation sites for corrosion. Electrochemical impedance study attributes this to the adverse effect of Al3Ti and TiB2 on the protective oxide surface film, which increases with immersion time.

Electropolymerization of Ni(salen) on carbon nanotube carrier as a capacitive material by pulse potentiostatic method

The composites of poly[Ni（salen）] and multi-walled carbon nanotube （MWCNT） were synthesized by pulse potentiostatic method. The composites were characterized by field emission scanning electron microscopy, Fourier transform infrared spectra, and electrochemical impedance spectroscopy. The wrapping of carbon nanotubes with poly[Ni（salen）] varied significantly with anodic pulse duration. Variance of structure of poly[Ni（salen）] caused by anodic pulse duration affected the ability of absorption to solvent molecules or solvated ions, which was indicated by v （C≡N） intensity. The ability to store/release charge of poly[Ni（salen）] caused by redox switching was evaluated in the form of low-frequency capacitance. Correlations of chargetransfer resistance/ionic diffusion resistance with potential and anodic pulse duration were investigated.

Electrochemical properties of Co-S/x wt.% AB_5 composite materials

The Co-S/x wt.% AB5 （x=0, 10, 20, 30） composite materials were prepared by simply mixing Co-S material fabricated by hy- drothermal method and AB5 alloy. The structure and morphology of the composite materials were characterized by XRD and SEM, respectively. The electrochemical properties of the composite electrodes were studied by the galvanostatic charge, dis- charge test and electrochemical impedance spectroscopy. The results showed that the Co-S/20 wt.% AB5 composite electrode showed the highest discharge capacity and the best cycling stability. The existence of the AB5 alloy improved the electro- chemical activity of composite electrodes, reduced the electrochemical polarization resistances and promoted the electrochem- ical conversion reaction between Co and Co（OH）2. In order to improve the utilization rate of active materials, 0.0! mol/L Na2S203 was added into the electrolyte. The electrochemical properties of the composite electrode were significantly enhanced. After fifty cycles, the discharge capacity of the composite electrode increased from 407 to 481.7 mAh/g and the capacity reten- tion increased from 79.7% to 91.2%.