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Exposed environments

The relative susceptibility of metals to atmospheric corrosion varies widely with the type of contaminant, e.g. zinc and cadmium, two metals that are used for the protection of steel in exposed environments, are both rapidly attacked by organic acidson the other hand, aluminium alloys resist attack by organic acids but may be rapidly corroded by chlorides, especially at crevices or areas of contact. [Pg.955]

Velocity Most metals and alloys are protected from corrosion, not by nobility [a metal s inherent resistance to enter into an electrochemical reaction with that environment, e.g., the (intrinsic) inertness of gold to (almost) everything but aqua regia], but by the formation of a protective film on the surface. In the examples of film-forming protective cases, the film has similar, but more limiting, specific assignment of that exemplaiy-type resistance to the exposed environment (not nearly so broad-based as noted in the case of gold). Velocity-accelerated corrosion is the accelerated or increased rate of deterioration or attack on a metal surface because of relative movement between a corrosive fluid and the metal surface, i.e., the instability (velocity sensitivity) of that protective film. [Pg.9]

Multicomponent pollutants in an aqueous environment and/or leachate of SWMs, which are COMs, usually consist of more than one pollutant in the exposed environment [1, 66-70]. Multicomponent adsorption involves competition among pollutants to occupy the limited adsorbent surface available and the interactions between different adsorbates. A number of models have been developed to predict multicomponent adsorption equilibria using data from SCS adsorption isotherms. For simple systems considerable success has been achieved but there is still no established method with universal proven applicability, and this problem remains as one of the more challenging obstacles to the development of improved methods of process design [34,71 - 76]. [Pg.178]

In more exposed environments, copper roofs and pipes quickly become covered in verdigris. Verdigris is green in colour (Figure 10.26) and is composed of copper salts formed on copper. The composition of verdigris varies depending on the atmospheric conditions, but includes mixed copper(n) carbonate and copper(n) hydroxide (CuC03.Cu(0H)2). [Pg.175]

Figure 10.26 Verdigris soon covers copper roofs in exposed environments. Figure 10.26 Verdigris soon covers copper roofs in exposed environments.
A9.4.3.5.3 The suitability of the inoculum for degrading the test substance depends on the presence and amount of competent degraders. When the inoculum is obtained from an environment that has previously been exposed to the test substance, the inoculum may be adapted as evidenced by a degradation capacity, which is greater than that of an inoculum from a non-exposed environment. As far as possible the inoculum... [Pg.466]

The kinetics of oxidation for each Met residue was determined by RP-FIPLC. The peak integration of the various oxidized forms taken at different time points was plotted as a function of time (Figure 3). After 60 minutes, about 90% of Met 28 and Met 60 were oxidized, while about 35% of Met 160 and essentially none of the Met 67, Met 90, and Met 132 residues had been converted to sulfoxide derivatives. The results indicate that Met 28 and Met 60 oxidize at a very rapid rate, while Met 160 was oxidized at a slightly slower rate. This data also suggests that Met 28 and Met 60 are located in an exposed environment on the surface of the protein and Met 160 may reside in a partially solvent-accessible environment. Met 67, Met 90, and Met 132 oxidize at substantially slower rates, suggesting that they reside at a buried environment that is relatively inaccessible to the oxidizing agent. [Pg.305]

Layered chemical sediments may contain a variety of dissolution features produced by contact with undersaturated waters such as rounded or truncated crystal surfaces, rounded dissolution cavities, and vertically-oriented dissolution pipes (Fig. 3D and 3E). The frequency and nature of these syndepositional dissolution features may be used to distinguish perennial saline lake deposits from saline pan (ephemeral lake) sediments (Li et al., 1996 Schubel Lowenstein, 1997). In very shallow water (centimeters deep) to subaerially-exposed environments, layered halite crusts have little to no protection from incoming... [Pg.192]

Concrete pours and aftercare Can the concrete works be precast and standardised as much as possible to reduce the amount of work undertaken in the exposed environment (Consider impacts on craneage requirements and associated risks) the design be made as simple as possible to avoid complex details/reinforcement fixing in an exposed environment formwork be designed to withstand wave loading reinforcement be deleted to avoid reinforcement fixing requirements ... [Pg.144]

In this protocol, direct surface analyses using IT-SIMS will be described from the perspective of analyses that were conducted to measure chemical warfare agents and related compounds (precursors, degradation products, and surrogates) that were adsorbed on samples from exposed environments. During the course of the research that is described in this chapter, the basic instrumental design of the IT-SIMS was modified for the analysis of absorbed compounds, and so the utilization of the instrument for these purposes is also described. [Pg.491]

Considering the multi-route and multimedia exposure of pesticides, the exposure assessment can be considered from three aspects (i) external (or potential) dose, (ii) internal or absorbed dose and (iii) biologically active dose. The external dose measurements determine the potential exposure of individuals or population. It involves a proper monitoring of the exposed environment, including air, water, food consumptions and workplace environment, to achieve an accurate quantification of the potential exposure of individuals. This kind of monitoring does not give information about the absorption of pesticides into the body. [Pg.436]

Iron dithiocarbamate is an important additive for producing photodegrad-able polyolefins which have time-controlled decay of their mechanical properties [116,124,1917,1920]. Their potential uses range from very shortlived materials such as packaging which is required to degrade in the environment immediately it is discarded, through protective films for annual crops, where a lifetime of several months is required, to a protective mulch for young trees, which may be required to stand up to 3-4 years in exposed environments before embrittlement. [Pg.375]


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See also in sourсe #XX -- [ Pg.90 ]




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