calomel
1.A TiO_2 thin film (made by hot oxidation method) works as the anode, high purity graphite works as the cathode, and a saturated calomel electrode (SCE) as reference electrode.
2.A three-electrode system composed of TiO_2 photoelectrode as the working electrode,Pt ring as the counter electrode and saturated calomel electrode (SCE) as the reference electrode was used for the photoelectrocatalytic degradation of phenol. The TiO_2 thin film photoelectrode was made by anodizing.
3.This paper reports the determenations of the mean activity coefficients of0. 000 mol· dm￣(-3)ZnSO_4 or CuSO_4,aqueous solutions in the temperature range from 10 to40℃ by emf method using a Zn─Hg or Cu electrode vs. Saturated calomel electrodes。
4.Cyclic voltammetry(CV)of Hb_montmorillonite films showed a pair of well defined and nearly reversible peaks at about-0.292V vs.saturated calomel electrode(SCE)at pH4.0,showing greatly facilitated direct electron transfer between Hb and PG electrodes in montmorillonite films.
5.The electrochemical capacitor with the high electrochemical activity sample as active material has the specific capacitance up to 177.5 F/g in the 0.5 mol/L Na 2SO 4 solution within 0～0.85 V SCE (saturated calomel electrode) potenitial.
6.A three-electrode system composed of TiO2/Ti prepared by sol-gel method as the working electrode,Pt wire as the counter electrode and saturated calomel electrode(SCE) as the reference electrode was used for the photoelectrocatalytic degradation of nitrobenzene.
7.In order to carry out this determination, a special pH glass elecctrode is made with SSAS 7312 sensitive glass invented by author. At same time, the general calomel electrode is replaced by plug form Ag/AgCl electrode characterized with high stability, and a new buffer solution used in "iso-point" calibration is also proposed.
8.Operated in a wall-jet configuration, a 300-μm diameter carbon-disk electrode was used as the working electrode, which exhibits a good response at +0.90 V (vs. saturated calomel electrode) for four analytes. Under the optimum conditions, the analytes were baseline separated within 20 min in a 50 mmol/1 borax buffer (pH 8.7).
