Design of On-Line Monitoring System for UHVDC Earth Electrode

At present the detecting of ultra high voltage direct current (UHVDC) earth electrode frequently uses manual inspection. This method can't get the real-time operational data of the earth electrodes, and meanwhile, the labor cost is very high. In order to satisfy the security needs of UHVDC, this paper designs an on-line monitoring system for UHVDC earth electrode. By 3G wireless communication-technologies, the system can monitor remotely many kinds of data such as the value of the grounding current, water level of the observation well, soil temperature and humidity near the earth electrode, the micro-climate around the earth electrode site, video data, etc. Through analyzing the datum, the system has broad prospect on fault detection and life evaluation of the UHVDC earth electrode.

Electro-catalytic degradation properties of Ti/SnO_2–Sb electrodes doped with different rare earths

Ti/SnO2–Sb electrode has a good effect on the removal of organic pollutants. But its short service life limits its large-scale application in industry. Electro-catalytic degradation performances and service life of the electrode can be significantly improved by doping rare earth（RE） ions into the oxide coating of Ti/SnO2–Sb electrode. Ti/SnO2–Sb electrodes doped with different RE elements（Ce, Dy, La, and Eu） were prepared by the thermal decomposition method at 550 ℃. Electro-catalytic degradation performances of electrodes doped with different RE elements were evaluated by linear sweep voltammetry（LSV） and Tafel curves. During the electrolysis,the conversion of p-nitrophenol was performed with these electrodes as anodes under galvanostatic control. The structures and morphologies of the surface coating of the electrodes were characterized by scanning electron microscope（SEM）. The results demonstrate that the electro-catalytic degradation performances of Ti/SnO2–Sb electrodes are improved to different levels by doping different RE ions. Improved Ti/SnO2–Sb electrodes by the introduction of different RE have higher oxygen evolution potential, better electro-catalysis ability, better coverage,and longer electrode life.

Preparation of Ce-TiO_2/carbon aerogel electrode and its performance in degradation of 4-chlorophenol

Ce-TiO2/CA（carbon aerogel） electrode was prepared by sol impregnation approach. The XRD（X-ray diffraction） and Raman spectra reveal that the TiO2 is anatase. The UV-vis diffuse reflectance spectra show that the optical absorption edge for Ce-TiO_2/CA is red-shifted to 535 nm compared with TiO_2/CA. Under visible light irradiation, the photocurrent density increment on Ce-TiO_2/CA is 75 times that on Ce-TiO_2/FTO（fluorine-doped tin oxide）. The electrochemical impedance spectroscopy reveals that the conductivity of CeTiO_2/CA is much better than the Ce-TiO_2/FTO. Furthermore, the Ce-TiO_2/CA can be used to the highest electrosorptive photodegradation for 4-chlorophenol wastewater degradation, which is ascribed predominantly to the efficient reduction of electron-hole pair recombination in the photocatalysts.

Cathodic reduction process of Al-Cu-Y alloy in fluoride-oxide eutectic system via molten salt electrolysis

Al-Cu-Y alloys were prepared by molten salt electrolysis in fluoride-oxide system composed of electrolyte（Na3 AlF6-AlF3-LiF-MgF2） and oxide（Al2 O3-CuO-Y2 O3）. Cathodic reduction process of Al2 O3,CuO and Y2 O3 were analyzed by cyclic voltammetry and chronoamperometry. Components and phase composition of alloy samples prepared by potentiostatic electrolysis were characterized by scanning electron microscopy and energy dispersive spectroscopy. The results show that the Al-Cu-Y alloy can be prepared in the AIF3-NaF-5 wt%LiF-5 wt%MgF2（NaF/AlF3 = 2.2, molecular ratio） eutectic system with mixed oxide（Al2 O3-CuO-Y2 O3） through 2 h at the conditions of a temperature of 1208 K, cell voltage3.0 V, cathode current density 0.7 A/cm^2. Al（Ⅲ） and Cu（Ⅱ） ions can be reduced to zero valence Al（0） and Cu（0） directly on carbonaceous electrode surface by instantaneous nucleation, respectively, the reduction process is controlled by diffusion. The reduction potential of Y（Ⅲ） ions is close to the active ions of fluoride melts, but strengthened phase AI3 Y can be formed through electrochemical reduction and alloyed process with active Al（Ⅲ） and Cu（Ⅱ） ions, meanwhile, the Al2 Cu and Al3 Y phases are distributed at the grain boundary of Al matrix.