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Electrochemical galvanic series

Aluminum alloys 2117,2017,2024 Mild steel (AISI 1018), wrought iron Cast iron, low-alloy high-strength steel Chrome iron (active) [Pg.590]

Hastelloy C (active). Inconel 625 (active), titanium (active) [Pg.591]

Titanium (pass.), Hastelloy C276 (passive). Inconel 625(pass.) [Pg.591]

The word ceramics is derived from the Greek keramos, meaning solid materials obtained from the firing of clays. According to a broader modern definition, ceramics are either crystalline or amorphous solid materials involving only ionic, covalent, or iono-covalent chemical bonds between metallic and nonmetallic elements. Well-known examples are silica and silicates, alumina, magnesia, calcia, titania, and zirconia. Despite the fact that, historically, oxides and silicates have been of prominent importance among ceramic materials, modern ceramics also include borides, carbides, silicides, nitrides, phosphides, and sulfides. [Pg.593]

As a general rule ceramic materials can be grouped into three main groups traditional ceramics, refractories and castables, and advanced or engineered ceramics. [Pg.593]


If dissimilar metals are placed in contact, in an electrolyte, the corrosion rate of the anodic metal will be increased, as the metal lower in the electrochemical series will readily act as a cathode. The galvanic series in sea water for some of the more commonly used metals is shown in Table 7.4. Some metals under certain conditions form a natural protective film for example, stainless steel in oxidising environments. This state is denoted by passive in the series shown in Table 7.4 active indicates the absence of the protective film. Minor... [Pg.289]

The position of magnesium in the electrochemical or galvanic series indicates that it has a potential of reacting chemically with a great number of other metals when there is electrical connection. The conductive path could be caused by direct metal-to-metal contact, an aqueous solution in which there is an electrolyte (e.g., chloride ions in solution), or by other ways. The key in any assembly involving magnesium is to design and assemble the parts in such a manner that the conductive path is eliminated. [Pg.354]

Figure 49 Electrochemical time series of galvanically coupled AA2024-T3 (ST) in 1 M NaCl. No deaeration and 0.01 cm2 exposure area, (a) Current and (b) open circuit potential. The horizontal dashed lines represent the mean pitting (top) and transition (bottom) potentials of high purity A1 at this Cl- concentration. (Data courtesy of Sheldon T. Prude, University of Virginia.)... Figure 49 Electrochemical time series of galvanically coupled AA2024-T3 (ST) in 1 M NaCl. No deaeration and 0.01 cm2 exposure area, (a) Current and (b) open circuit potential. The horizontal dashed lines represent the mean pitting (top) and transition (bottom) potentials of high purity A1 at this Cl- concentration. (Data courtesy of Sheldon T. Prude, University of Virginia.)...
Galvanic compatibility is an important consideration for choosing materials for hydrogen systems. It is based on the relative position of metals in what is called the electrochemical series, galvanic series or electromotive series. [Pg.385]

The corrosion of metals and semi-conductors involves the flow of an electric current within the material. Most of the constituent materials in fibrous laminates are insulators and in consequence, electrochemical corrosion is negligible. But graphite acts as a noble metal, lying between platinum and titanium in the galvanic series [104]. Carbon fibres have a structure which is essentially similar to graphite, being described as turbostratic (the... [Pg.253]

One or more electrochemical cells connected in series constitute an electrical battery . Primary electrochemical (galvanic) cells are ready to produce current immediately and do not need to be charged in the way secondary cells (described below) do. In disposable cells, the chemical half reactions are not easily reversible, so the cells cannot be reliably recharged. Common disposable cells include the zinc-carbon cells and the alkaline cells. Secondary electrochemical cells contain the active materials in the disclWged state, so they must be charged before use. The oldest form of rechargeable cell is the lead-acid battery. [Pg.274]

Galvanic Corrosion that is electrochemical in nature. Galvanic corrosion is caused by placing two dissimilar metals in contact with each other, directly or ough a conductive fluid. The rate of this type of corrosion increases with the distance between the metals in the galvanic series (see Table 3-2). The further apart the metals, the more rapidly the anodic material will corrode. Variations of galvanic corrosion include... [Pg.93]

The galvanic series of aluminum alloys and other metals representative of their electrochemical behavior in seawater and in most natural waters and atmospheres is shown in Table 19.6. The effect of alloying elements in determining the position of aluminum alloys in the series is shown in Figure 19.4. These elements, primarily copper and zinc, affect electrode potential only when they are in solid solution. [Pg.511]

Galvanic series Table of electrochemical potentials (voltage) associated with the ionization of metal atoms. These are called Nernst potentials. [Pg.670]

Thermodynamic principles can help explain a corrosion situation in terms of the stability of chemical species and reactions associated with corrosion processes. However, thermodynamic calculations cannot be used to predict corrosion rates. When two metals are put in contact, they can produce a voltage, as in a battery or electrochemical cell (see Galvanic Corrosion in Sec. 5.2.1). The material lower in what has been called the galvanic series will tend to become the anode and corrode, while the material higher in the series will tend to support a cathodic reaction. Iron or aluminum, for example, will have a tendency to corrode when connected to graphite or platinum. What the series cannot predict is the rate at which these metals corrode. Electrode kinetic principles have to be used to estimate these rates. [Pg.32]

Nevertheless, the introduction of SKPFM measurements reveals the need to estabhsh galvanic series for microstructures or elements of galvanic couples involved in localized corrosion at the micrometer scale. But the introduction of SKPFM data on numerical simulation seems to be not possible as a large doubt always exists. It justifies the interest to focus on in-situ local microelectro-chemical studies for investigating the cmrent-potential relation in an aqueous solution, i.e., the electrochemical kinetic at the scale of the microstructure. [Pg.251]

Concept Check 17.7 Tin cans are made of a steel, the inside of which is coated with a thin layer of tin. The tin protects the steel from corrosion by food products in the same manner as zinc protects steel from atmospheric corrosion. Briefly explain how this cathodic protection of tin cans is possible, given that tin is electrochemically less active than steel in the galvanic series (Table 172). [Pg.709]


See other pages where Electrochemical galvanic series is mentioned: [Pg.590]    [Pg.591]    [Pg.590]    [Pg.591]    [Pg.217]    [Pg.510]    [Pg.192]    [Pg.485]    [Pg.404]    [Pg.1386]    [Pg.368]    [Pg.241]    [Pg.496]    [Pg.164]    [Pg.57]    [Pg.239]    [Pg.239]    [Pg.555]    [Pg.650]    [Pg.657]    [Pg.854]    [Pg.40]    [Pg.492]    [Pg.675]    [Pg.5]    [Pg.492]    [Pg.442]    [Pg.16]    [Pg.256]    [Pg.925]    [Pg.134]    [Pg.11]    [Pg.55]    [Pg.1076]   
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