Phosphate electrode

Awad, S. A. and Kamel, K. M. Behaviour of Tin as Metal-metal Phosphate Electrode and Mechanism of Promotion and Inhibition of its Corrosion by Phosphate Ions , Journal of Electroanalytical Chemistry, 24, 217-25 (1969)... 

Liteanu and Hopirtean described a polyvinylchloride-tricresyl phosphate electrode as being responsive to Ag, H, ngj" ", Na", and Although the electrodes composed of polymeric films directly on metals are attractive from the viewpoint of simplicity, the mechanism of their function remains to be elucidated, and the scope of their applications remains to be studied. 

Srinivasan V, Newman J (2004) Discharge model Jot the lithium iron-phosphate electrode. J Electrochem Soc 15LA1517-A1529... 

Active immobilized enzyme used in the production of a phosphate electrode Comparison of methods for the hydrophobic immobilization of enzymes with retention of activity... 

Wang, G. X. et ai. Physical and electrochemical properties of doped lithium iron phosphate electrodes. Eiectrochim.Acta 50,443 (2004). 

Srinivasan, V. Newman, J. Discharge model for the lithium iron-phosphate electrode./. Electrochem. Soc., 151, A1517-A1529 [2004). 

Kim DH, Kang JW, Jung lO, Lim IS, Kim EJ, Song SJ, Lee JS, Kim J (2008) Microwave assisted synthesis of nanocrystalline Fe-phosphates electrode materials and their electrochemical propperties. J Nanosci Nanotechnol 8 5376-5379... 

One example of a liquid-based ion-selective electrode is that for Ca +, which uses a porous plastic membrane saturated with di-(n-decyl) phosphate (Figure 11.13). As shown in Figure 11.14, the membrane is placed at the end of a nonconducting cylindrical tube and is in contact with two reservoirs. The outer reservoir contains di-(n-decyl) phosphate in di- -octylphenylphosphonate, which soaks into the porous membrane. The inner reservoir contains a standard aqueous solution of Ca + and a Ag/AgCl reference electrode. Calcium ion-selective electrodes are also available in which the di-(n-decyl) phosphate is immobilized in a polyvinyl chloride... 

Operation and Control. Control of a chromium phosphate conversion coating bath requires monitoring chromium and aluminum concentrations, active fluoride level, and temperature. Coating weight is very sensitive to active, ie, uncomplexed, fluoride. An innovative electrochemical method using a siHcon electrode (25) is employed for measuring active fluoride. A special precaution in chromium phosphate bath operation is the... 

Combination silver—silver salt electrodes have been used in electrochemistry. The potential of the common Ag/AgCl (saturated)—KCl (saturated) reference electrode is +0.199 V. Silver phosphate is suitable for the preparation of a reference electrode for the measurement of aqueous phosphate solutions (54). The silver—silver sulfate—sodium sulfate reference electrode has also been described (55). 

Sodium and chloride may be measured using ion-selective electrodes (see Electro analytical techniques). On-line monitors exist for these ions. Sihca and phosphate may be monitored colorimetricaHy. Iron is usually monitored by analysis of filters that have had a measured amount of water flow through them. Chloride, sulfate, phosphate, and other anions may be monitored by ion chromatography using chemical suppression. On-line ion chromatography is used at many nuclear power plants. 

Hardness can also be calculated by summation of the individually deterrnined alkaline earths by means of atomic absorption analysis. Basic samples must be acidified, and lanthanum chloride must be added to minimise interferences from phosphate, sulfate, and aluminum. An ion-selective electrode that utilizes ahquid ion exchanger is also available for hardness measurement however, this electrode is susceptible to interferences from other dissolved metal ions. 

A typical modem phosphorus fumace (12 m diameter) can produce some 4 toniKs per hour and is rated at 60-70 MW (i.e. 140000A at SOOV). Three electrodes, each weighing 60 tonnes, lead in the current. The amounts of raw material required to make 1 tonne of white phosphorus depend on their purity but are typically 8 tonnes of phosphate rock. 2 tonnes of silica, 1.5 tonnes of coke, and 0.4 tonnes of electrode carbon. The phos rfKmis vapour is driven off from the top of the fumace together with the CO and some H2 it is passed through a hot electrostatic precipitator to remove dust and then condensed by water sprays at about 70 (P4 melts at 44.T). The byproduct CO is used for supplementary heating. 

Modification of the top electrode may also be achieved. This was done by adding a small amount of surfactant, such as an ether phosphate or an ether sulfate, to the spin-coal solution of the luminescent polymer [89[. The lipophobic ether chains segregate at the surface of the (predominantly) hydrocarbon polymer, becoming available for complexation with the aluminum cathode which is deposited on top. Thus, the dipole in the surfactant points away from the electrode and lowers its work function to improve the injection of electrons. 

When the electrode is placed in an aqueous solution of glucose which has been suitably diluted with a phosphate buffer solution (pH 7.3), solution passes through the outer membrane into the enzyme where hydroxen peroxide is produced. Hydrogen peroxide can diffuse through the inner membrane which, however, is impermeable to other components of the solution. The electrode vessel contains phosphate buffer, a platinum wire and a silver wire which act as electrodes. A potential of 0.7 volts is applied to the electrodes (the apparatus shown in Fig. 16.17 is suitable) with the platinum wire as anode. At this electrode the reaction H202->02 + 2H+ +2e takes place, and the oxygen produced is reduced at the silver cathode ... 

Instead of immobilizing the antibody onto the transducer, it is possible to use a bare (amperometric or potentiometric) electrode for probing enzyme immunoassay reactions (42). In this case, the content of the immunoassay reaction vessel is injected to an appropriate flow system containing an electrochemical detector, or the electrode can be inserted into the reaction vessel. Remarkably low (femtomolar) detection limits have been reported in connection with the use of the alkaline phosphatase label (43,44). This enzyme catalyzes the hydrolysis of phosphate esters to liberate easily oxidizable phenolic products. 

Figure 5 shows the relationship between the passive film thickness of an iron electrode and the electrode potential in an anodic phosphate solution and a neutral borate solution.6,9 A passive film on an iron electrode in acidic solution is made up of an oxide barrier layer that increases its thickness approximately linearly with increasing electrode potential, whereas in a neutral solution, there is a precipitated hydroxide layer with a constant thickness outside the oxide barrier layer. 

FIG. 26 Cyclic voltammograms of 40 monolayers of Langmuir-Schaefer films of cytochrome P450SCC on indium-tin oxide glass plate (ITO) in 10 mM phosphate buffer at a scan rate of 20 mV/s between 0.4 and —0.4 V vs. Ag/AgCl. LS films on ITO worked as the working electrode, platinum as the counter, and Ag/AgCl as the reference electrode. Cholesterol dissolved in X-triton 100 was added 50 p.1 at a time (1) with cholesterol, (2) 50 p.1 of cholesterol, (3) 100 p.1 cholesterol, and (4) 150 p.1 of cholesterol. 

---