Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Electrode stainless steel

CV of solutions of lithium bis[ salicy-lato(2-)]borate in PC shows mainly the same oxidation behavior as with lithium bis[2,2 biphenyldiolato(2-)-0,0 ] borate, i.e., electrode (stainless steel or Au) passivation. The anodic oxidation limit is the highest of all borates investigated by us so far, namely 4.5 V versus Li. However, in contrast to lithium bis[2,2 -biphenyl-diolato(2-)-0,0 Jborate based solutions, lithium deposition and dissolution without previous protective film formation by oxidation of the anion is not possible, as the anion itself is probably reduced at potentials of 620-670 mV versus Li, where a... [Pg.478]

To date very little is known about tool wear. The two major causes of tool wear are chemical etching and anodic dissolution. The discharge activity at the tool-electrode may also cause some tool wear, but to date this has never been quantified. Based on the author s personal experience, tool wear is not a serious problem, and even after machining with the same tool-electrode (stainless steel) for several hours, no significant tool-wear could be measured. [Pg.158]

Figure 6.6.5 Application of cyclic voltammetry to in vivo analysis in brain tissue, (a) Carbon paste working electrode, stainless steel auxiliary electrode (18-gauge cannula), Ag/AgCl reference electrode, and other apparatus for voltammetric measurements, (b) Cyclic voltammogram for ascorbic acid oxidation at C-paste electrode positioned in the caudate nucleus of an anesthetized rat. [From P. T. Kissinger, J. B. Hart, and R. N. Adams, Brain Res., 55, 20 (1973), with permission.]... Figure 6.6.5 Application of cyclic voltammetry to in vivo analysis in brain tissue, (a) Carbon paste working electrode, stainless steel auxiliary electrode (18-gauge cannula), Ag/AgCl reference electrode, and other apparatus for voltammetric measurements, (b) Cyclic voltammogram for ascorbic acid oxidation at C-paste electrode positioned in the caudate nucleus of an anesthetized rat. [From P. T. Kissinger, J. B. Hart, and R. N. Adams, Brain Res., 55, 20 (1973), with permission.]...
Detector UV 280 E, Laboratorni Pristroje ADLC 2 detector, carbon fiber working electrode, stainless steel counter electrode, 1.1 V vs Ag/AgCl reference electrode, 0.6% Na2HPO4.12H20 added to mobile phase which was adjusted to pH 6.0-6.05 with acetic acid... [Pg.573]

Noble mebds such as platinum-iridium are also utilized in pacemaker electrodes. In addition to the noble metals, stainless steel and tantalum can also be used in sensing (nonpacing) electrodes. Stainless steel has also been used as wire braids and reinforcements in catheters, particularly in high-pressure catheters, such as those used for radiopaque dye injection. [Pg.331]

Semi-dry transfer For the semi-dry transfer, the gel-membrane sandwich is placed between carbon plate electrodes. Semi-dry or horizontal blotting uses two plate electrodes (stainless steel or graphite/ carbon) for a uniform electrical field over a short distance, and sandwiches between these of up to six gel/membrane/filter paper assemblies, all well soaked in transfer buffer. The assembly is clamped or otherwise secured on its side and electrophoretic transfer effected in this position, using as transfer buffer only the liquid contained in the gel and filter papers or other pads in the assembly. [Pg.1015]

Column 125x5 (i.d.) mm Spherisorb SSW silica Eluent Methanolic ammonium perchlorate (10 mmol L, apparent pH 6.7 - see Chapter 4, Section 1) Flowrate 2.0 mL min Working electrode V25 Grade glassy carbon Reference electrode Ag/AgCl Auxiliary electrode stainless steel Maximum useable applied potential for biological extracts +1.2 V... [Pg.65]

Flow system for total cyanide analysis by ASTM Method D 7511-09e2. Detector silver working electrode, Ag/AgCI reference electrode, stainless steel counter electrode IV Injection valve RC reaction coll. [Pg.192]

Additional measurements (Ferris and Mellman, 1967) were carried out using 0.1m KCl and the following electrodes stainless steel, bright platinum, sandblasted platinum, platinized platinum two-parallel-disc electrodes, and disc-and-opposing-point electrodes. The impedance bridge used was limited in the amount of current which it could supply to the electrolytic cell. By using one point electrode, it was possible to increase the current density by several orders of magnitude. The results were consistent with Schwan and Maczuk s prior work. [Pg.21]

Concentric with the annulus are compartments formed in the rotor and stator which contain the electrodes (stainless steel) and their electrolytes. These are isolated from the carrier solution by dialysis membranes of regenerated cellulose which are supported on inert porous tubes. An electric field is applied across the electrodes, typically 30 V at 60 A. [Pg.378]

Counter electrode Stainless steel Stainless steel Stainless steel... [Pg.698]

A concentration of 6 Xg/mL of dye in water was used in all cases. This concentration was chosen because it was found to show best results without overloading the sensitivity of the detector. Absorbance was measured continuously using a submersible fiber optic cell, supplied witb tbe PC600 colorimeter. Current between tbe two electrodes (stainless steel and platinum) was measured continuously, using a picoammeter. Typically, 5 - 15,000 Volts were used which resulted in a current of Ca. 10 to 50 xA. Current fluctuations of Ca. 10% were often present. [Pg.26]

Fig. 9.5 (a) Structures of the ionic liquids, (b) Photograph of gel polymer electrolyte with a diameter of 13 mm and a thickness of 200 pm. (c) Conductivity Arrhenius plots of four gel polymer membranes. The data are obtained from impedance spectroscopy at 10-50 °C. (d) Composition, conductivity data, and ECW of gel polymer electrolytes with varied ionic liquids, mp melting point, EON electrochemical window electrodes, stainless steel/stainless steel first cycle v = 25 mV/s T=50 °C potential range, E vs Stainless Steel= 4 V [57]... [Pg.295]

In tenns of an electrochemical treatment, passivation of a surface represents a significant deviation from ideal electrode behaviour. As mentioned above, for a metal immersed in an electrolyte, the conditions can be such as predicted by the Pourbaix diagram that fonnation of a second-phase film—usually an insoluble surface oxide film—is favoured compared with dissolution (solvation) of the oxidized anion. Depending on the quality of the oxide film, the fonnation of a surface layer can retard further dissolution and virtually stop it after some time. Such surface layers are called passive films. This type of film provides the comparably high chemical stability of many important constmction materials such as aluminium or stainless steels. [Pg.2722]

Electromagnetic flow meters ate avadable with various liner and electrode materials. Liner and electrode selection is governed by the corrosion characteristics of the Hquid. Eor corrosive chemicals, fluoropolymer or ceramic liners and noble metal electrodes are commonly used polyurethane or mbber and stainless steel electrodes are often used for abrasive slurries. Some fluids tend to form an insulating coating on the electrodes introducing errors or loss of signal. To overcome this problem, specially shaped electrodes are avadable that extend into the flow stream and tend to self-clean. In another approach, the electrodes are periodically vibrated at ultrasonic frequencies. [Pg.65]

Corrective action should be initiated when value is > — 0.23 V against the standard hydrogen electrode (SHE). Plant-specific values should be estabUshed for protection of stainless steels and nickel-based critical components. [Pg.195]

The vertical tube (water-cooled) generator consists of two concentric tubes the outer of which is cooled with water and acts as the ground electrode. Feed gas is introduced into the top of the inner stainless steel tube (which serves as the high voltage electrode), exits at the bottom of the outer tube, flows upward through the aimular space (which contains the electric discharge), and emerges at the top of the outer tube into a product gas manifold. [Pg.500]

Greater deviations which are occasionally observed between two reference electrodes in a medium are mostly due to stray electric fields or colloid chemical dielectric polarization effects of solid constituents of the medium (e.g., sand [3]) (see Section 3.3.1). Major changes in composition (e.g., in soils) do not lead to noticeable differences of diffusion potentials with reference electrodes in concentrated salt solutions. On the other hand, with simple metal electrodes which are sometimes used as probes for potential controlled rectifiers, certain changes are to be expected through the medium. In these cases the concern is not with reference electrodes, in principle, but metals that have a rest potential which is as constant as possible in the medium concerned. This is usually more constant the more active the metal is, which is the case, for example, for zinc but not stainless steel. [Pg.87]

The polarization cell is an electrochemical component in which nickel or stainless steel electrodes are immersed in 50% KOH solution [9]. With ac, the... [Pg.340]

Electrochemical cells are assembled in the glove-box. The cell is a 2320-type coin cell (23 mm OD and 2.0 mm thickness) as schematically shown in Fig. 5. The cell includes the electrolyte, the cell cap and can which are stainless steel, a polypropylene gasket used to seal the cell, the two electrodes, the separator between the electrodes, as well as a stainless spacer and a mild steel disc spring which are used to increase the pressure on the electrodes. Once the cell is assembled in the right order, the cell is sealed by a pressure crimper inside the glove-box. [Pg.352]

Spiral-plate exchangers are fabricated from any material that can be cold worked and welded. Materials commonly used include carbo steel, stainless steel, nickel and nickel alloys, titanium, Hastelloys, and copper alloys. Baked phenolic-resin coatings are sometimes applied. Electrodes can also be wound into the assembly to anodically protect surfaces against corrosion. [Pg.36]


See other pages where Electrode stainless steel is mentioned: [Pg.655]    [Pg.308]    [Pg.655]    [Pg.308]    [Pg.891]    [Pg.190]    [Pg.191]    [Pg.311]    [Pg.375]    [Pg.429]    [Pg.176]    [Pg.239]    [Pg.499]    [Pg.376]    [Pg.504]    [Pg.281]    [Pg.1811]    [Pg.2009]    [Pg.301]    [Pg.65]    [Pg.67]    [Pg.117]    [Pg.261]    [Pg.74]    [Pg.220]    [Pg.351]    [Pg.176]    [Pg.1025]   
See also in sourсe #XX -- [ Pg.254 , Pg.255 ]




SEARCH



Charging electrode, stainless steel

Electrochemical impedance spectroscopy stainless steel electrode

Electrochemical sensors stainless steel electrode

© 2019 chempedia.info