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Surface Film Effects

Ermakov SA, Zujkova AM, Panchenko AR, Salashin SG, Talipova TG, Titov VI (1986) Surface film effect on short wind waves. Dyn Atmos Oceans 10 31-50 Ermakov SA, Zujkova AM, Salashin SG (1987) Transformation of short wind wave spectra in film slicks. Izv Acad Sci USSR, FAO 23 707-715 (in Russian)... [Pg.312]

SURFACE FILM EFFECTS ON DEFORMATION BEHAVIOR OF IRON SINGLE CRYSTALS AT CRYOGENIC TEMPERATURES ... [Pg.144]

Surface Film Effects on Deformation Behavior of Iron Single Crystals... [Pg.145]

The goal of lubrication is elimination of this wear and minimizing friction otherwise encountered in dry sliding. This is accompHshed ideally with complete separation of the mbbing surfaces with a full film of lubricant. When complete hill-film separation is impossible, surface chemical effects of a lubricating oil and its additives, or solid-film lubricants such as graphite and molybdenum sulfide, can assist. [Pg.234]

In neutral and alkaline environments, the magnesium hydroxide product can form a surface film which offers considerable protection to the pure metal or its common alloys. Electron diffraction studies of the film formed ia humid air iadicate that it is amorphous, with the oxidation rate reported to be less than 0.01 /rni/yr. If the humidity level is sufficiently high, so that condensation occurs on the surface of the sample, the amorphous film is found to contain at least some crystalline magnesium hydroxide (bmcite). The crystalline magnesium hydroxide is also protective ia deionized water at room temperature. The aeration of the water has Httie or no measurable effect on the corrosion resistance. However, as the water temperature is iacreased to 100°C, the protective capacity of the film begias to erode, particularly ia the presence of certain cathodic contaminants ia either the metal or the water (121,122). [Pg.332]

The relinking (14) and self-healing film (3) theories require chemical interaction between the antiozonant and ozonized mbber. The evidence for these interactions is meager (35,36). Overall, there seems to be no clear evidence in the Hterature for PDA derivatives becoming attached to mbber chains as a result of ozone attack. Much fundamental work in this area remains to be done, however. It seems clear at this point that any antiozonant—mbber interaction must be much less important than the scavenging effect of the antiozonant. In summary, the scavenger model is beheved to be the principal mechanism of antiozonant action. Ozone—antiozonant reaction products form a surface film that provides additional protection (37). [Pg.238]

Electrolytic corrosion occurs in regions I and IV with the formation of soluble iron ions. Solid corrosion products which can have a protective effect are formed in region II. This is the region of surface film passivity. Certain corrosive sub-... [Pg.39]

The effects of alternating currents are much less of a corrosion danger than those of direct currents. Experiments on steel have shown that during the positive half wave [34-37] only about 1 % contributes to the dissolution of iron according to Eq. (2-21). The remaining 99% is involved in the discharge of capacitances, of redox systems (e.g., Fe /Fe in surface films) or in the evolution of Oj by... [Pg.150]

In contrast to external protection, the anodes in internal protection are usually more heavily covered with corrosion products and oil residues because the electrolyte is stagnant and contaminated. The impression can be given that the anodes are no longer functional. Usually the surface films are porous and spongy and can be removed easily. This is achieved by spraying during tank cleaning. In their unaltered state they have in practice little effect on the current output in ballast seawater. In water low in salt, the anodes can passivate and are then inactive. [Pg.412]

It should be clearly pointed out that with anodic interference according to the data in Fig. 2-6 in Section 2.2.4.1, the corrosivity of the electrolyte for the particular material has no influence on the current exit corrosion. On the other hand, the conductivity of the electrolyte has an effect according to Eqs. (24-102) and (20-4). Chemical parameters have a further influence that determines the formation of surface films and the polarization resistance. [Pg.445]

Strained set of lattice parameters and calculating the stress from the peak shifts, taking into account the angle of the detected sets of planes relative to the surface (see discussion above). If the assumed unstrained lattice parameters are incorrect not all peaks will give the same values. It should be borne in mind that, because of stoichiometry or impurity effects, modified surface films often have unstrained lattice parameters that are different from the same materials in the bulk form. In addition, thin film mechanical properties (Young s modulus and Poisson ratio) can differ from those of bulk materials. Where pronounced texture and stress are present simultaneously analysis can be particularly difficult. [Pg.217]

Surface roughness effects in inorganic primer films... [Pg.446]

This treatment is known as sizing. As mentioned earlier, the joint between the matrix and the fibre is critical if the reinforcement is to be effective and so the surface film on the glass ensures that the adhesion will be good. [Pg.169]

As shown in Chap. 7, shock compression introduces large numbers of defects which in turn cause substantial increases in solid state reactivity. Such shock activation is obviously critical to the process. One of the most direct effects of the mechanical deformation is the removal of oxides or other surface films from the surfaces of the powders. It is well recognized that such surface films can greatly inhibit chemical reaction. The very large mechanical deformation would be expected to substantially damage, if not completely remove, such films. Other manifestations of shock activation are shown in the next chapter. Effects have been shown that represent many orders of magnitude of change in solid state reactivity. [Pg.146]

The elements of Group 5 are in many ways similar to their predecessors in Group 4. They react with most non-metals, giving products which are frequently interstitial and nonstoichiometric, but they require high temperatures to do so. Their general resistance to corrosion is largely due to the formation of surface films of oxides which are particularly effective in the case of tantalum. Unless heated, tantalum is appreciably attacked only by oleum, hydrofluoric acid or, more particularly, a hydrofluoric/nitric acid mixture. Fused alkalis will also attack it. In addition to these reagents, vanadium and niobium are attacked by other hot concentrated mineral acids but are resistant to fused alkali. [Pg.979]

Medwell, J. O. and A. A. Nicol, Surface Roughness Effects on Condensate Films, ASME-AlChE Heat Trans. Conference and Exhibit, Los Angeles, California, Aug. (1965), Paper No. 65-HT-43. [Pg.287]

Macroscopic heterogeneities, e.g. crevices, discontinuities in surface films, bimetallic contacts etc. will have a pronounced effect on the location and the kinetics of the corrosion reaction and are considered in various sections throughout this work. Practical environments are shown schematically in Fig. 1.3, which also serves to emphasise the relationship between the detailed structure of the metal, the environment, and external factors such as stress, fatigue, velocity, impingement, etc. [Pg.11]

Firstly, they might be expected to have an effect when corrosion occurs under conditions of active (film-free) anodic dissolution and is not limited by the diffusion of oxygen or some other species in the environment. However, if the rate of active dissolution is controlled by the rate of oxygen diffusion, or if, in general terms, the rate-controlling process does not take place at the metal surface, the effect of crystal defects might be expected to be minimal. [Pg.36]

If oxidising salts are present in neutral solutions they may reduce corrosion of the iron by the establishment of thin protective films on the metal surface. Their effectiveness is considerably diminished if much chloride ion is also present in solution. [Pg.595]

The irons are most useful in environments containing a plentiful supply of oxygen or oxidising agents anaerobic or reducing conditions may lead to rapid corrosion. Physical effects such as abrasion or sudden dimensional changes induced by temperature fluctuations may rupture the film and allow corrosion to take place. The iron will also be subject to corrosion by solutions containing anions, such as those of the halides, which can penetrate surface films relatively readily. [Pg.614]


See other pages where Surface Film Effects is mentioned: [Pg.21]    [Pg.428]    [Pg.666]    [Pg.229]    [Pg.22]    [Pg.21]    [Pg.428]    [Pg.666]    [Pg.229]    [Pg.22]    [Pg.113]    [Pg.723]    [Pg.266]    [Pg.244]    [Pg.1202]    [Pg.2369]    [Pg.2435]    [Pg.40]    [Pg.59]    [Pg.257]    [Pg.195]    [Pg.108]    [Pg.273]    [Pg.280]    [Pg.148]    [Pg.695]    [Pg.208]   


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