Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Natural passivation

Aluminium anodes comprise essentially three generic types Al-Zn-In, Al-Zn-Hg and Al-Zn-Sn. Since Al-Zn-Sn alloys have largely been superseded, they will not be discussed further. Indium and mercury are added to aluminium to act as activators, i.e. to overcome the natural passivation of aluminium. Despite this, aluminium anodes are not suitable for low chloride environments which would lead to passivation. These anodes are therefore not used for land-based applications (although examples of use in environments such as swamps do exist). Similarly their use in low chloride aqueous environments such as estuaries must be viewed with caution. [Pg.150]

Since the natural passivity of aluminium is due to the thin film of oxide formed by the action of the atmosphere, it is not unexpected that the thicker films formed by anodic oxidation afford considerable protection against corrosive influences, provided the oxide layer is continuous, and free from macropores. The protective action of the film is considerably enhanced by effective sealing, which plugs the mouths of the micropores formed in the normal course of anodising with hydrated oxide, and still further improvement may be afforded by the incorporation of corrosion inhibitors, such as dichromates, in the sealing solution. Chromic acid films, in spite of their thinness, show good corrosion resistance. [Pg.697]

The Natural Passivation and Corrosion of Metals and Alloys XPS studies of the air-formed natural passive layer on aluminium surfaces have identified a number of hydroxides as well as alumina (Barr, 1977). The oxidation of pure iron and of stainless steels and other iron alloys have also been extensively... [Pg.31]

Natural (passive) cooling of PV receiver for low ratio concentration 3.5-5 or active cooling with combined electric generation—hot water production for concentration 5-30 is used. [Pg.88]

Passive immunity occurs when the patient receives antibodies from another source rather than generating his or her own antibodies. Newborns have natural passive immunity to protect them from pathogens. The newborn receives natural passive immunity from antibodies that cross the placenta. Antibodies may... [Pg.345]

Calcium chloride has the ability to break down the natural passivity provided by Portland cement concrete and thereby encourage the corrosion of reinforcement or other embedded metal. [Pg.9]

Upper Surface. All ESCA spectra for the upper surface of the brown leaves show that they are covered by a layer dominated by the hydrocarbon parts of the cuticle material, which is incapable of preventing significant amounts of air-induced oxidation. Although reduced in comparison to the other leaf surfaces, the limited amount of oxygen found by grazing incidence is predominantly on the outermost surface. The waxy esterified parts of the cuticle appear to be dissipated and thus, as previously mentioned, all surfaces exposed to air, even the most non-reactive, are subject to at least some O2- and H20-induced oxidation. Thus, what we call natural passivation is indicative of extensive oxidation, which prevents further corrosive oxidation [33, 202]. Hence, in the case of the brown leaf we observe the botanical equivalent of metal corrosion. [Pg.182]

All of the analyses put together suggest that our brown leaf has a surface first dominated by naturally passivated hydrocarbon deposits, with more passivation on the bottom of the leaf than on its top. All this is of course interesting, but it is a very limited study. From this limited study we cannot be certain as to what is tran-... [Pg.182]

Several metals, such as chromium, are naturally passive when exposed to the atmosphere, and they remain bright and tamish-free for years, in contrast to iron and copper, which corrode or tarnish in short time. It is found that the passive property of chromium is conferred on alloys of Cr-Fe, provided that >12wt.% Cr is present. Iron-base alloys containing a minimum of 12wt.% Cr are known as the stainless steels. [Pg.100]

Figure 15.3 shows fhe currenf response over time for individual solid particle impacts on the naturally passivating system of stainless steel. Some impacts will only result in partial passive layer removal or cracking which will influence repassivation kinetics and possibly the composition and thickness of the regrown layer. [Pg.284]

Passivity is an electrochemical reduction mechanism that occurs on a metal-electrolyte interface. The resultant reduction product is a solid film of a metal oxide compound having a stoichiometric reaction (a reaction that goes to completion) based on the corroding metal. Thus, passivity occurs on metals that are active-passive by natural passivation without the influence of external potentials or artificial passivation due an applied external anodic potential. [Pg.178]

The potential range where only a low current is observed is the passive region. Natural passivation therefore occurs if, in the solution, there is a species (e,g. oxygen or a redox reagent) capable of taking the surface potential into the passive region (the surface potential is calculated from the Nemst equation for the redox reagent couple). [Pg.507]

Underfloor natural (passive) venting wherever possible (or car park). Where passive ventilation is not feasible or cost effective use active venting or positive pressurisation... [Pg.154]

Barriers can be designed to be passive or active in nature. Passive safety barriers provide a natural fixed roadblock, such as a tank pit or a firewall. Active barriers provide a response to certain states or conditions they involve a sequence of detection, diagnosis, and action (also referred to as detect-diagnose-deliect). Both physical and nonphysical barriers are utilized and apphed in hazard control and risk mitigation. Anything used to control. [Pg.36]

Mioced-metal anodes also utilize titanium, niobium, and tantalum as substrate materials. A film of oxides is formed on these substrates, with protective properties similar to the passive film forming on the substrate materials. The important difference is that whereas the natural passive film is an effective electrical insulator, the mixed metal oxide surface film passes anodic current. The product forms are similar to those of the platinized anodes. These anodes are typically used with carbonaceous backfill. Electrode consumption is usually not the critical factor in determining anode life rather the formation of nonconductive oxides between the substrate and the conductive surface film limits effective functioning. Excessive current densities accelerate the buildup of these insulating oxides to unacceptable levels. [Pg.883]

Polarisation curves for aluminium do not have the same shape as for steel (Figure B. 1.13). There is no domain of passivity, because aluminium is naturally passive. [Pg.101]

Aluminium is naturally passive and, therefore, does not need to be passivated, unlike certain metals such as steel. A metal that can be passivated has undergone a chemical... [Pg.101]

When protective films are easily formed on the metal surface by exposure to air, the metal is naturally in the passive state and corrosion resistant. Many metals, however, have to be protected by alloying with one of the naturally passive metals, e.g. chromium or aluminium. In other words, the naturally passive metals have very low passivation current they form their protective coating rather quickly when current is applied to them. When they are alloyed with corroding metals, they lower the passivation current of the latter and help to form a pore free inhibitive oxide layer. [Pg.189]

Electropohshing, as well as acid treatments, charge the steel surface with hydrogen, and for UHV applications the stainless steel should be vacuum baked at 1000°C for several hours to outgas hydrogen taken up by the surface. The surface of staiidess steel will form a natural passive oxide layer 10-20 A thick when dried and exposed to the ambient. [Pg.123]


See other pages where Natural passivation is mentioned: [Pg.19]    [Pg.230]    [Pg.111]    [Pg.306]    [Pg.225]    [Pg.230]    [Pg.253]    [Pg.254]    [Pg.77]    [Pg.690]    [Pg.7]    [Pg.267]    [Pg.129]    [Pg.729]    [Pg.730]    [Pg.8]   
See also in sourсe #XX -- [ Pg.178 ]




SEARCH



© 2024 chempedia.info