Method to determine vented electrochemical cell quality

Cell mass is measured periodically or monitored continuously by balances and clocks to determine water loss and rate of mass loss during trickle charge period

Alkaline electrochemical cells and method of making

Equilibrated cellulose ether membranes of increased electrolytic conductivity for use as separators in concentrated alkaline electrochemical cells are investigated. The method of making such membranes by equilibration to the degree desired in an aqueous alkali solution mantained at a temperature below about 10 C is described

In situ scanning electrochemical probe microscopy for energy applications

High resolution electrochemical imaging methods provide opportunities to study localized phenomena on electrode surfaces. Here, we review recent advances in scanning electrochemical microscopy (SECM) to study materials involved in (electrocatalytic) energy-related applications. In particular, we discuss SECM as a powerful screening technique and also advances in novel techniques based on micro- and nanopipets, such as the scanning micropipet contact method and scanning electrochemical cell microscopy and their use in energy-related research

Silicate determination in sea water: toward a reagentless electrochemical method

ilicate has been determined in sea water by four different electrochemical methods based on the detection of the silicomolybdic complex formed in acidic media by the reaction between silicate and molybdenum salts. The first two methods are based on the addition of molybdate and protons in a seawater sample in an electrochemical cell. Cyclic voltammetry presents two reduction and two oxidation peaks giving four values of the concentration and therefore increasing the precision. Then chronoamperometry is performed on an electrode held at a constant potential. A semi-autonomous method has been developed based on the electrochemical anodic oxidation of molybdenum, the complexation of the oxidation product with silicate and the detection of the complex by cyclic voltammetry. This method is tested and compared with the classical colorimetric one during ANT XXIII/3 cruise across Drake Passage (January–February 2006). The detection limit is 1 μM and the deviation between both methods is less than 3% for concentrations higher than 10 μM. Finally a complete reagentless method with a precision of 2.6% is described based on the simultaneous formation of the molybdenum salt and protons in a divided electrochemical cell. This latter method should be very useful for developing a reagentless sensor suitable for long term in situ deployments on oceanic biogeochemical observatories

Resonant frequency measurements as an alternative to phase-selective A.C. polarography in tensammetry and pseudocapacitance determinations

A new method is proposed for the determination of the double-layer capacitance and pseudocapacitance of electrochemical cells. The method is based on the measurement of the resonant frequency of the circuit consisting of the electrochemical cell connected in series with a standard inductor. The performance of the method is demonstrated with double-layer capacitance measurements at the dropping mercury electrode in 1 M KCl and butanol-1/1 M KCl mixtures and with the determination of heterogeneous charge-transfer rate constants ranging from 10−2 to 10−5 m s−1

Electrochemical coulometer and method of forming same Patent

Alkaline-type coulometer cell for primary charge control in secondary battery recharge circuit

The temperature variation of hydrogen diffusion coefficients in metal alloys

Hydrogen diffusion coefficients were measured as a function of temperature for a few metal alloys using an electrochemical evolution technique. Results from these measurements are compared to those obtained by the time-lag method. In all cases, diffusion coefficients obtained by the electrochemical method are larger than those by the time-lag method by an order of magnitude or more. These differences are attributed mainly to hydrogen trapping