Passive attack

Two basic mechanisms cause biological corrosion. Biologically produced substances may actively or passively cause attack. Each mechanism either accelerates preexisting corrosion or establishes a new form of metal loss. Often the distinction between active and passive attack is vague. 

In passive attack, biological material acts as a chemically inert substance. Wastage is an indirect consequence of the biological mass or biological by-products. Biomass acts as any deposit accumulation would,... 

Passive attack involving underdeposit corrosion tends to involve large system surface areas and, hence, accounts for the greatest amount of metal loss, by weight, in cooling water systems. Active attack tends to produce intense localized corrosion and, as such, a greater incidence of perforations. 

Passive attack beneath slime is usually general, and rusting on steel may color surfaces brown and red (Fig. 6.14). If sulfate reducers are present, pitting may be superimposed on the generally corroded surface (see Fig. 6.2). 

Given the low concentration and means of dispersal, the Tokyo subway sarin attack can be referred to as a passive attack. The implication of such an assumption is therefore that mankind has not yet witnessed a full-scale sarin attack in any major city. While valuable information can certainly be gained from the Tokyo subway sarin attack, the experience obtained from the more aggressive Matsumoto sarin attack and the Iran-Iraq war should also be considered when developing initiatives directed at dealing with a potential full-scale attack in the future where the effects will be more serious. 

Known-message attack (or general passive attack) The attacker is given the public key and some signed messages. 

Restricted attacks. In the model with indirect access, one can model restricted attacks if one needs them. For instance, passive attacks are modeled by honest users that do not react on anything from the outside world, but choose their inputs, e.g., the messages they authenticate, according to some predefined probability distribution. This is unrealistic in most situations. A better example might be that honest users choose some initialization parameters carefully and without influence from outside, but may be influenced later. 

Security attack is defined as any action, intended or not, that compromises the security of the information and/or system. Attacks can generally be passive or active. Passive attacks can be the copying of information or a traffic analysis. Active attacks involve some modification of the original data or fabrication of new data, such as replay or interruption of data. Security mechanisms are designed to prevent, protect, and recover from security attacks. Since no technique is able to provide full protection, the designers and/or system administrators of a network are responsible for choosing and implementing different security mechanisms. 

This section provides the results of a preliminary experimental campaign conducted with respect to settings detailed in Table 2. In our experiments we compared the behavior of the network in safe conditions and under the attack, both in the case of an unmodified AODV stack and when the T R layer is deployed. It is worth noting that to make measurements comparable we implemented a passive sinkhole attack. In a passive attack, the attacker does not inject additional packets, rather it executes the attack by modifying legitimate traffic. 

Strong oxidising acids, for example hot concentrated sulphuric acid and nitric acid, attack finely divided boron to give boric acid H3CO3. The metallic elements behave much as expected, the metal being oxidised whilst the acid is reduced. Bulk aluminium, however, is rendered passive by both dilute and concentrated nitric acid and no action occurs the passivity is due to the formation of an impervious oxide layer. Finely divided aluminium does dissolve slowly when heated in concentrated nitric acid. 

The following mechanisms in corrosion behavior have been affected by implantation and have been reviewed (119) (/) expansion of the passive range of potential, (2) enhancement of resistance to localized breakdown of passive film, (J) formation of amorphous surface alloy to eliminate grain boundaries and stabilize an amorphous passive film, (4) shift open circuit (corrosion) potential into passive range of potential, (5) reduce/eliminate attack at second-phase particles, and (6) inhibit cathodic kinetics. 

Sometimes the formation of oxide films on the metal surface binders efficient ECM, and leads to poor surface finish. Eor example, the ECM of titanium is rendered difficult in chloride and nitrate electrolytes because the oxide film formed is so passive. Even when higher (eg, ca 50 V) voltage is apphed, to break the oxide film, its dismption is so nonuniform that deep grain boundary attack of the metal surface occurs. 

The anodes can be made of graphite which tolerates high current densities without passivation, but are subject to gradual corrosive attack causing a... 

Most mineral acids react vigorously with thorium metal. Aqueous HCl attacks thorium metal, but dissolution is not complete. From 12 to 25% of the metal typically remains undissolved. A small amount of fluoride or fluorosiUcate is often used to assist in complete dissolution. Nitric acid passivates the surface of thorium metal, but small amounts of fluoride or fluorosiUcate assists in complete dissolution. Dilute HF, HNO, or H2SO4, or concentrated HCIO4 and H PO, slowly dissolve thorium metal, accompanied by constant hydrogen gas evolution. Thorium metal does not dissolve in alkaline hydroxide solutions. 

Titanium is susceptible to pitting and crevice corrosion in aqueous chloride environments. The area of susceptibiUty for several alloys is shown in Figure 7 as a function of temperature and pH. The susceptibiUty depends on pH. The susceptibiUty temperature increases paraboHcaHy from 65°C as pH is increased from 2ero. After the incorporation of noble-metal additions such as in ASTM Grades 7 or 12, crevice corrosion attack is not observed above pH 2 until ca 270°C. Noble alloying elements shift the equiUbrium potential into the passive region where a protective film is formed and maintained. 

MetaUic cobalt dissolves readily in dilute H2SO4, HCl, or HNO to form cobaltous salts (see also Cobalt compounds). Like iron, cobalt is passivated by strong oxidizing agents, such as dichromates and HNO, and cobalt is slowly attacked by NH OH and NaOH. 

An especially insidious type of corrosion is localized corrosion (1—3,5) which occurs at distinct sites on the surface of a metal while the remainder of the metal is either not attacked or attacked much more slowly. Localized corrosion is usually seen on metals that are passivated, ie, protected from corrosion by oxide films, and occurs as a result of the breakdown of the oxide film. Generally the oxide film breakdown requires the presence of an aggressive anion, the most common of which is chloride. Localized corrosion can cause considerable damage to a metal stmcture without the metal exhibiting any appreciable loss in weight. Localized corrosion occurs on a number of technologically important materials such as stainless steels, nickel-base alloys, aluminum, titanium, and copper (see Aluminumand ALUMINUM ALLOYS Nickel AND nickel alloys Steel and Titaniumand titanium alloys). 

Electroforrning is the production or reproduction of articles by electro deposition upon a mandrel or mold that is subsequendy separated from the deposit. The separated electro deposit becomes the manufactured article. Of all the metals, copper and nickel are most widely used in electroforming. Mandrels are of two types permanent or expendable. Permanent mandrels are treated in a variety of ways to passivate the surface so that the deposit has very Httie or no adhesion to the mandrel, and separation is easily accompHshed without damaging the mandrel. Expendable mandrels are used where the shape of the electroform would prohibit removal of the mandrel without damage. Low melting alloys, metals that can be chemically dissolved without attack on the electroform, plastics that can be dissolved in solvents, ate typical examples. 

Short-time tests also can give misleading results on alloys that form passive films, such as stainless steels. With Borderline conditions, a prolonged test may be needed to permit breakdown of the passive film and subsequently more rapid attack. Consequently, tests run for long periods are considerably more reahstic than those conducted for short durations. This statement must be quahfied by stating that corrosion should not proceed to the point at which the original specimen size or the exposed area is drastic y reduced or the metal is perforated. 

The CBD diagram can provide various lands of information about the performance of an aUoy/medium system. The technique can be used for a direc t calculation of the corrosion rate as well as for indicating the conditions of passivity and tendency of the metal to suffer local pitting and crevice attack. 

There is often a period before corrosion starts in a crevice in passivating metals. This so-called incubation period corresponds to the time necessary to establish a crevice environment aggressive enough to dissolve the passive oxide layer. The incubation period is well known in stainless steels exposed to waters containing chloride. After a time period in which crevice corrosion is negligible, attack begins, and the rate of metal loss increases (Fig. 2.8). 

Pitting is also promoted by low pH. Thus, acidic deposits contribute to attack on stainless steels. Amphoteric alloys such as aluminum are harmed by both acidic and alkaline deposits (Fig. 4.4). Other passive metals (those that form protective corrosion product layers spontaneously) are similarly affected. 

Silt, sand, concrete chips, shells, and so on, foul many cooling water systems. These siliceous materials produce indirect attack by establishing oxygen concentration cells. Attack is usually general on steel, cast iron, and most copper alloys. Localized attack is almost always confined to strongly passivating metals such as stainless steels and aluminum alloys. 

Generally, pitting corrosion only occurs on passivated metals when the passive film is destroyed locally. In most cases chloride ions cause this local attack at potentials U > U q. Bromide ions also act in the same way [51], The critical potential for pitting corrosion UpQ is called the pitting potential. It has the same significance as in Eqs. (2-39) and (2-48). 

Pits occur as small areas of localized corrosion and vary in size, frequency of occurrence, and depth. Rapid penetration of the metal may occur, leading to metal perforation. Pits are often initiated because of inhomogeneity of the metal surface, deposits on the surface, or breaks in a passive film. The intensity of attack is related to the ratio of cathode area to anode ai ea (pit site), as well as the effect of the environment. Halide ions such as chlorides often stimulate pitting corrosion. Once a pit starts, a concentration-cell is developed since the base of the pit is less accessible to oxygen. 

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