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Corrosiveness, salt selection

Studies have been conducted on the effects of corrosive salt-spray environment on bondlines of different bonded systems. The system variations included clad and bare alloys, surface treatments, adhesive primers, and adhesives. Five specimens were fabricated for each of the bonded systems. The specimens were then placed in a salt-spray environment of 5% NaCl at 35 °C. The change in wedge-test crack length of each specimen was recorded periodically. At the end of 1 month, one specimen was randomly selected from each bonded system and opened for visual inspection of the bondline condition, both in the stressed zone (crack-tip zone) and in the unstressed zone. The same procedure was carried out after 2, 3, 6, and 12 months, when the last specimen was removed from test. The conclusions were as follows... [Pg.252]

While the ambient-temperature operation of membrane processes reduces scaling, membranes are much more susceptible not only to minute amounts of scaling or even dirt, but also to the presence of certain salts and other compounds that reduce their ability to separate salt from water. To reduce corrosion, scaling, and other problems, the water to be desalted is pretreated. The pretreatment consists of filtration, and may include removal of air (deaeration), removal of CO2 (decarbonation), and selective removal of scale-forming salts (softening). It also includes the addition of chemicals that allow operation without scale deposition, or which retard scale deposition or cause the precipitation of scale which does not adhere to soHd surfaces, and that prevent foam formation during the desalination process. [Pg.242]

Table 4.9 Selected inorganic salts highly corrosive to carbon steel (Corrosion rate >50 mpy)... Table 4.9 Selected inorganic salts highly corrosive to carbon steel (Corrosion rate >50 mpy)...
Mobile-phase selection for cationic polymers is similar to that for the other polymers in that ionic strength and pH can change the shape of the solute from linear to globular (9). Mobile phases are often low pH e.g., 0.1% trifluo-roacetic acid, including 0.2 M sodium chloride, has been used successfully for polyvinylpyridines. Sodium nitrate can be substituted for the chloride to avoid corrosive effects. Some salt must be included so that ion exclusion does not occur (3). [Pg.316]

It is not worth while, therefore, to give a digest of experimentally determined corrosion rates , but Table 2.21 indicates some sources of such data and their nature. (Some references to data on compatibility of fused salts with non-metallic materials have been included for the sake of completeness.) It should be remembered, that in the case of alloys, failure usually arises from selective attack which causes porosity of the container, even though the wall may appear on casual inspection to be quite sound... [Pg.441]

The stability of tin over the middle pH range (approximately 3-5-9), its solubility in acids or alkalis (modified by the high hydrogen overpotential), and the formation of complex ions are the basis of its general corrosion behaviour. Other properties which have influenced the selection of tin for particular purposes are the non-toxicity of tin salts and the absence of catalytic promotion of oxidation processes that may cause changes in oils or other neutral media affecting their quality or producing corrosive acids. [Pg.803]

For environments in which tin is less readily corroded than lead, corrosion resistance of the alloy decreases as the lead content increases the decrease may, in some circumstances, be sharp at a particular composition. In the more corrosive media, such as nitrite solution, a sharp increase of corrosion rate is observed as the lead content increases beyond 30waters with low contents of dissolved salts, the corrosion rate increases slowly with lead content up to about 70% and then rises more steeply, but in the general run of supply waters the ability of lead to form protective insoluble anodic products is helpful to the durability of solder. Selective dissolution of tin has been... [Pg.807]

Selection of Corrosion-Resistant Materials The concentrated sofutions of acids, alkalies, or salts, salt melts, and the like used as electrolytes in reactors as a rule are highly corrosive, particularly so at elevated temperatures. Hence, the design materials, both metallic and nonmetallic, should have a sufficiently high corrosion and chemical resistance. Low-alloy steels are a universal structural material for reactors with alkaline solutions, whereas for reactors with acidic solutions, high-alloy steels and other expensive materials must be used. Polymers, including highly stable fluoropolymers such as PTFE, become more and more common as structural materials for reactors. Corrosion problems are of particular importance, of course, when materials for nonconsumable electrodes (and especially anodes) are selected, which must be sufficiently stable and at the same time catalytically active. [Pg.329]

Copper is attacked by mineral acids, except cold, dilute, unaerated sulphuric acid. It is resistant to caustic alkalies, except ammonia, and to many organic acids and salts. The brasses and bronzes have a similar corrosion resistance to the pure metal. Their main use in the chemical industry is for valves and other small fittings, and for heat-exchanger tubes and tube sheets. If brass is used, a grade must be selected that is resistant to dezincification. [Pg.299]

Post-combustion capture using chemical absorption by aqueous alkaline amine solutions has been used for C02 and H2S removal from gas-treating plants for decades [6]. Amines react rapidly, selectively and reversibly with C02 and can be applied at low C02 partial pressure conditions. Amines are volatile, cheap and safe in handling. They show several disadvantages as they are also corrosive and require the use of resistant materials. Furthermore, amines form stable salts in the presence of O2, SOx and other impurities such as particles, HC1, HF and organic and inorganic Fig trace compounds that extremely constrain the content of those compounds in the treated gas. [Pg.84]

These incorporate membranes fabricated from insoluble crystalline materials. They can be in the form of a single crystal, a compressed disc of micro-crystalline material or an agglomerate of micro-crystals embedded in a silicone rubber or paraffin matrix which is moulded in the form of a thin disc. The materials used are highly insoluble salts such as lanthanum fluoride, barium sulphate, silver halides and metal sulphides. These types of membrane show a selective and Nemstian response to solutions containing either the cation or the anion of the salt used. Factors to be considered in the fabrication of a suitable membrane include solubility, mechanical strength, conductivity and resistance to abrasion or corrosion. [Pg.238]

Ionic liquids are, quite simply, liquids that are composed entirely of ions. Thus, molten sodium chloride is an ionic liquid a solution of sodium chloride in water (a molecular solvent) is an ionic solution. The term ionic liquids was selected with care, as it is our belief that the more commonly used phrase molten salts (or simply melts) is referential, and invokes a flawed image of these solvents as being high-temperature, corrosive, viscous media (cf. molten cryolite). The reality is that room-temperature ionic liquids can be liquid at temperatures as low as — 96°C, and are typically colorless, fluid, and easily handled. To use the term molten salts to describe these novel systems is as archaic as describing a car as a horseless carriage. Moreover, in the patent and recent academic literature, ionic... [Pg.111]


See other pages where Corrosiveness, salt selection is mentioned: [Pg.434]    [Pg.613]    [Pg.580]    [Pg.178]    [Pg.184]    [Pg.334]    [Pg.328]    [Pg.211]    [Pg.250]    [Pg.365]    [Pg.124]    [Pg.1137]    [Pg.24]    [Pg.128]    [Pg.1259]    [Pg.476]    [Pg.902]    [Pg.4]    [Pg.63]    [Pg.400]    [Pg.440]    [Pg.1122]    [Pg.54]    [Pg.157]    [Pg.331]    [Pg.22]    [Pg.141]    [Pg.262]    [Pg.259]    [Pg.195]    [Pg.72]    [Pg.274]    [Pg.258]    [Pg.328]   
See also in sourсe #XX -- [ Pg.613 ]




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Salt corrosion

Selective corrosion

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