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Subject seawater reaction

Pitting corrosion always remains a worthy subject for study, particularly with reference to mechanism, and the problem conveniently divides into aspects of initiation and growth. For 6061 alloy in synthetic seawater, given sufficient time, pit initiation and growth will occur at potentials at or slightly above the repassivition potential . In an electrochemical study, it was found that chloride ions attack the passive layer as a chemical reaction partner so that the initiation process becomes one of cooperative chemical and electrochemical effects . [Pg.676]

A significant amount of seawater is trapped in the open spaces that exist between the particles in marine sediments. This fluid is termed pore water or interstitial water. Marine sediments are the site of many chemical reactions, such as sulfate reduction, as well as mineral precipitation and dissolution. These sedimentary reactions can alter the major ion ratios. As a result, the chemical composition of pore water is usually quite different from that of seawater. The chemistry of marine sediments is the subject of Part 111. [Pg.64]

The pattern in Figure 34 has considerable implications for our understanding of past climate, but is still subject to debate. The models of Muehlenbachs (1998) and Gregory (1991) claimed that due to a balance of high and low temperature reactions during interaction of the water cycle with the lithosphere, the of the oceans should have been buffered near its present-day value. If seawater always had of 0%o... [Pg.3856]

The total mass of oxygen consumed by the reactions listed, added to that contained in the atmosphere, sums to about 3.1 x 1019 kg. The result provides a reasonable balance between production and losses only because we have made an effort to maximize the oxygen consumption. On the whole, the budget is subject to much uncertainty and is as yet unsatisfactory. But the data show that the major reservoirs of oxygen are sulfate in seawater and in evaporites, and Fe203 in sedimentary rocks. Only 4% of total oxygen resides in the atmosphere. One must appreciate the peculiarity of this distribution. Since oxidative weathering causes a steady drain on 02, we can understand its presence in the atmosphere only if it is continuously... [Pg.617]

Most of the inorganic anions of seawater are not subject to primary photochemical processes, because their electronic excitation energies lie well above the maximum photon energy available in sea surface sunlight. Nitrate and nitrite do, however, exhibit weak transitions with meixima at 303 nm (e ax 7 mole cm ) and 355 nm (e ax = 22.5 mole" cm" ), respectively. The primary photoreactions of both of these oxyanions produce free radical products in seawater (Zafiriou and True, 1979a, b). The overall reactions are ... [Pg.317]

Manganese oxides are also subject to reductive dissolution by light in surface seawaters. This process produces Mn(II), which is kinetically stable to oxidation in the absence of bacteria that are subject to photoinhibition. These two effects lead to the formation of a surface maximum in soluble Mn(II), in contrast to most metals which are depleted in surface waters due to biological removal processes. Other examples of the impact of photochemical reactions on trace metal chemistry are provided in Further Reading. [Pg.95]

The preparation of LDHs has been the subject of over 50 patents. The claims are specific variants of the general methods previously described, including coprecipitation (148), anion exchange (149), preparation from oxides and hydroxides (150-152), reaction of metal oxides or hydroxides with a salt (152-154), and precipitation via aluminate (115-118,120,155). The principal material described is Mg/Al LDH carbonate however, other anions, such as those composed of heavy metal complexes (120,149), alcoholates (156), anionic surfactants (148), phosphates (148,157), and halides (115,158a), have also been claimed. LDH can also be produced by controlled addition of Ca(OH)2 and AICI3 to seawater (158b). [Pg.392]

Sulfate attack. Concrete in contact with ground water in clays may be subjected to attack by the sulfate salts of calcium, magnesium and sodium. Sulfate salts are also present in seawater and brackish water. Following are the major reactions ... [Pg.615]


See other pages where Subject seawater reaction is mentioned: [Pg.539]    [Pg.65]    [Pg.352]    [Pg.445]    [Pg.119]    [Pg.136]    [Pg.141]    [Pg.496]    [Pg.539]    [Pg.322]    [Pg.349]    [Pg.204]    [Pg.3054]    [Pg.327]    [Pg.621]    [Pg.99]    [Pg.94]    [Pg.132]    [Pg.327]    [Pg.91]    [Pg.463]    [Pg.588]    [Pg.761]   
See also in sourсe #XX -- [ Pg.183 ]




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