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Aeration elements

Using a simple test arrangement, it can show that different metal surface aeration in oxygen corrosion results in the formation of local aeration elements. [Pg.548]

Far more critical is plug-type dezinciflcation, which mainly arises in heat exchanger tubes upon deposition of sand grains, oil residues, rust, mussels, and algae with formation of aeration elements. Even thick tubes can be perforated in this way. Dezinciflcation can be impeded by adding small amount of arsenic or phosphorus. [Pg.563]

The different levels of oxygen access in the different water zones may, in extensive structures, for example sheet pilings or mooring posts, lead to the formation of aeration elements. Measurements have shown that the cathodic areas are usually on or just above the waterline [53]. The result is then increased corrosion in the tidal zone, which may be much larger than would be expected based on the different rusting rates in samples exposed separately in the tidal and immersion zones. [Pg.201]

Much more complex and difficult than the usually relatively small samples with approx. 0.02 nf surface are long samples with exposure extending from the splash zone (SZ) through the tidal zone (TZ) and into the immersion zone (IZ) or even into the silt zone/sea floor. Since the large-area aeration elements may form on such samples as described above, it can be expected that the results of corrosion tests in such long samples will differ clearly from those obtained with small individual samples. [Pg.201]

The principal elements of the system include an aeration tank in which the wastewater is thoroughly mixed with continuously activated sludge and oxygen. From this part of the process, it passes into a clarifier tank, where the settled sludge is removed from the purified water to be recycled by the return activated sludge pumps. [Pg.167]

In 1976, Hodes et al. [85] reported the stabilization of polycrystalline CdSe photoelectrodes (prepared by electrodeposition and subsequent heat treatment) in de-aerated alkaline aqueous or organic (not specified) solution of S , in which some elemental sulfur was dissolved. It was claimed that besides CdSe, other semiconductors such as CdS, CdTe (n- and p-types), ZnSe, or Bi2S3 are also stable as photoelectrodes in a polycrystalline form in the sulfide solution, and that such cells under AMI sunlight are stable over periods of months, a rather exaggerated claim. It was described in addition how a part or all of the converted energy could be stored in a controlled way in the system by the introduction of an electrode of porous silver. [Pg.229]

Possible causes of sludge bulking include (a) absence of certain necessary trace elements in wastewater (b) wide fluctuations in wastewater pH (c) limited DO in the aeration tank (d) inadequate FIM ratio (e) inadequate mean cell residence time Tc (f) inadequate return sludge pumping rate (g) internal plant overloading and (h) poor sedimentation clarifier operation. [Pg.1183]

Whatever its previous history before disposal and deposition at a site, the alteration of bone buried or exposed to the elements is determined, mainly, by the combined effect of the physical, chemical, and biological conditions at the site where it is deposited these include the seasonal characteristics, average temperature, relative humidity, amount and flow motion of water, pH value, extent of aeration, and the nature of the microorganism population (Millard 2001 White and Hannus 1983). [Pg.410]

The Simple Forms in Which Main Group Biological Elements Occur in Aerated Soil, Water, Rivers, Lakes and Sea (or in Blood Plasma)... [Pg.45]

This gum was the first microbial gum to be used in the food industry. It is produced by the aerobic fermentation of Xanthomonas campestris. A specially selected culture is grown on a carbohydrate-containing nutrient medium with a nitrogen source and other essential elements. The pH, temperature and aeration are controlled carefully. The product is then sterilised and the gum is precipitated with propan-2-ol. Next, the precipitate is washed, then pressed to remove residual alcohol, followed by drying and grinding to the required size. [Pg.130]

In well-aerated soil, it is expected that all species will be in their highest oxidation states. However, this does not happen for reasons elucidated in previous chapters. In well-aerated soil, both ferrous and ferric iron can exist along with elemental iron.3 Zinc, copper, and especially manganese can apparently exist in a mixture of oxidation states simultaneously in soil. Add to this a multitude of organic species that are also capable of oxidation-reduction reactions and the result is truly a complex voltammetric system [12,13],... [Pg.204]

Figure 3. Layout of the design elements (cells), with the aeration cascade on the right-hand-side. Figure 3. Layout of the design elements (cells), with the aeration cascade on the right-hand-side.
Alternatively, raw anode slimes are aerated with hot dilute sulfuric acid to remove copper. Slimes are then mixed thoroughly with sodium carbonate and roasted in the presence of sufficient air. Sodium selenate formed is leached with water. Hydrochloric acid is added to this selenate solution. Treatment with sulfur dioxide precipitates elemental selenium. Alternatively, the selenate solution is evaporated to dryness. Sodium selenate is reduced to sodium selenide by heating with carbon at high temperatures. Sodium selenide is leached with water. Air is blown over the solution. Selenide is oxidized to elemental selenium which precipitates. [Pg.813]

C. The element Co is a hard lustrous bluish-white metal which acquires a somewhat inert coat of C03O4 in air or aerated HOH. It is not further reactive with HOH, air, or bases, but dissolves slowly in non-oxidizing acids and rapidly in dilute oxidizing acids to give pink Co+. When finely powdered, Co heated in air gives black C03O4. [Pg.360]

Hydrogen sulfide enters natural waters from decay of organic matter (e.g., in swamps), bacterial reduction of sulfate ion, or underground sour natural gas deposits. It can be removed by aeration, anion exchange (Eq. 14.14), or oxidation by chlorine to elemental sulfur ... [Pg.279]


See other pages where Aeration elements is mentioned: [Pg.409]    [Pg.548]    [Pg.556]    [Pg.334]    [Pg.165]    [Pg.210]    [Pg.211]    [Pg.568]    [Pg.409]    [Pg.742]    [Pg.409]    [Pg.548]    [Pg.556]    [Pg.334]    [Pg.165]    [Pg.210]    [Pg.211]    [Pg.568]    [Pg.409]    [Pg.742]    [Pg.78]    [Pg.166]    [Pg.195]    [Pg.993]    [Pg.1018]    [Pg.62]    [Pg.163]    [Pg.168]    [Pg.145]    [Pg.276]    [Pg.81]    [Pg.132]    [Pg.397]    [Pg.183]    [Pg.617]    [Pg.285]    [Pg.479]    [Pg.199]    [Pg.298]    [Pg.215]    [Pg.81]    [Pg.132]    [Pg.685]    [Pg.559]   
See also in sourсe #XX -- [ Pg.201 ]




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