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Water iron content

The stabilised nitrate may then be bleached with sodium hypochlorite, centrifuged to remove much of the water in which the polymer has been slurried and dehydrated by displacement with alcohol while under pressure in a press. It is interesting to note that in these processes approximately 35 000 gallons (160000 litres) of water are used for every ton of cellulose nitrate produced. Control of purity of the water is important in particular the iron content should be as low as 0.03 parts per million since iron can adversely affect both the colour and heat stability of the polymer. [Pg.617]

Apart from the oxygen corrosion that results in HW and LP steam heating systems where water losses occur as a result of leaking pump mechanical seals, excess BD, faulty steam traps, and other sources, a subsequent effect is the development of fouling. This effect stems from the production of corrosion debris and (high iron content) sludge that eventually settle out in the boiler. This corrosion debris, sludge, and other foulants must be periodically removed from the boiler by BD, which merely adds to the water loss, and the cycle perpetuates. [Pg.181]

The various sizes and types utilize single-bar, multifield, multipole magnets singly or in factory assembled bar-bundles. They are further designed for easy disassembly and cleaning in systems with existing corrosion build-up or iron content in the water. ... [Pg.338]

The Rieske protein II (SoxF) from Sulfolobus acidocaldarius, which is part, not of a bci or b f complex, but of the SoxM oxidase complex 18), could be expressed in E. coli, both in a full-length form containing the membrane anchor and in truncated water-soluble forms 111). In contrast to the results reported for the Rieske protein from Rhodobacter sphaeroides, the Rieske cluster was more efficiently inserted into the truncated soluble forms of the protein. Incorporation of the cluster was increased threefold when the E. coli cells were subject to a heat shock (42°C for 30 min) before induction of the expression of the Rieske protein, indicating that chaperonins facilitate the correct folding of the soluble form of SoxF. The iron content of the purified soluble SoxF variant was calculated as 1.5 mol Fe/mol protein the cluster showed g values very close to those observed in the SoxM complex and a redox potential of E° = +375 mV 111). [Pg.146]

We have developed an efficient and practical method for clean oxidation of starch (21-23) resulting in the oxidation of primary alcohol function in Ce position and the cleavage of vicinal diols in C2 and C3 position (Figure 30.2). We used small amounts of cheap iron tetrasulfophthalocyanine catalyst, pure water as reaction medium and H2O2 as clean oxidant to achieve a one-pot conversion of starch resulting in the introduction of aldehyde and carboxyl functions in polymer chains. The iron content... [Pg.266]

Fig. 6.3. Saturation indices of Amazon River water with respect to various minerals (left) calculated directly from a chemical analysis, and (right) computed assuming that equilibrium with kaolinite and hematite controls the fluid s aluminum and iron content. Fig. 6.3. Saturation indices of Amazon River water with respect to various minerals (left) calculated directly from a chemical analysis, and (right) computed assuming that equilibrium with kaolinite and hematite controls the fluid s aluminum and iron content.
When the post-coagulation sludge is added to hydrolyzate production, then the iron hydroxide is converted into ferric sulfate, which is well soluble in water. Too high content of soluble iron compounds, which are easily absorbable, should be avoided, as the excessive amount of the iron in the diet is harmful [13]. It leads to some disease like hemochromatosis or siderosis. Thus, the aim of our research was to find a method of decreasing the absorbable iron content of fish silage. [Pg.218]

A water sample was tested for iron content, but was diluted prior to obtaining the instrument reading. This dilution involved taking 10.00 mL of the sample and diluting it to 100.00 mL. If the instrument reading gave a concentration of 0.891 ppm for this diluted sample, what is the concentration in the undiluted sample ... [Pg.164]

After analysis for iron content, a water sample was found to have a concentration of 4.62 ppm iron. How many milligrams of iron are contained in 100.0 mL of the water ... [Pg.177]

Prepare calibration standards of 1.0,2.0,3.0, and 4.0 ppm iron from the 100 ppm stock in 50-mL volumetric flasks, but do not dilute to the mark until step 6. Also prepare a flask for the blank (no iron). If real water samples are being analyzed and you expect the iron content to be low, prepare two additional standards that are 0.1 and 0.5 ppm. [Pg.197]

A similar flow sheet has been suggested for the treatment of mine waters. However, the similarity is only apparent. The iron content in these... [Pg.620]

The physical and chemical parameters which influence iron oxide formation vary with time and space, e. g. through changing water/air content. Microenvironments exist in pores of different sizes and with different degrees of filling. For example, hematite was identified in coatings at the (dry) surface of a basalt boulder, whereas goethite occurred in a nearby (moister) crack (Bender-Koch et al., 1995 a). In another case, goethite was the dominant oxide next to the root surface, whereas lepidocrocite predominated a few mm away from it (Schwertmann Fitzpatrick, 1977). Often, however, the exact conditions under which Fe oxides form are difficult to determine. [Pg.434]

Figure 5.50 compares the real time constant voltage anodization behavior of the Ti-Fe films, with the samples identified by their iron content, anodized at 30 V in EG -h 0.3 wt % NH4F -1- 2.0 % de-ionized water a systematic variation in anodization behavior is seen with decreasing Fe content. The sharp drop in the anodization current in the first 100 s is due to the formation of an initial electrically insulating... [Pg.341]

Elemental composition Fe 27.93%, S 24.06%, O 48.01%. The water of crystallization in the hydrate salt may be determined by gravimetry. Iron content of the salt may be determined by common instrumental techniques (See Iron). Sulfate can be analyzed in an aqueous solution of the salt by gravimetry or colorimetry after addition of barium chloride solution. [Pg.439]

Figure 1. Data from the literature indicate that S concentrations in surface lake sediments are poorly correlated with A, lake-water sulfate concentrations (104 lakes) B, sediment carbon content (78 lakes) or C, sediment iron content (22 lakes). Sulfur concentrations in lake sediments typically are lower than concentrations in marine sediments of comparable carbon content (upper line in B). The lower line in B represents the average C S ratio (55) reported in seston (59, 72, 27, 56, 78). Most of the lake sediments reported in the literature have more iron than sulfur. (Data are from references 24-30, 34, 48—51, 55-57, 59-61, 71, 104, 112, 199, 205, 222, and 223.)... Figure 1. Data from the literature indicate that S concentrations in surface lake sediments are poorly correlated with A, lake-water sulfate concentrations (104 lakes) B, sediment carbon content (78 lakes) or C, sediment iron content (22 lakes). Sulfur concentrations in lake sediments typically are lower than concentrations in marine sediments of comparable carbon content (upper line in B). The lower line in B represents the average C S ratio (55) reported in seston (59, 72, 27, 56, 78). Most of the lake sediments reported in the literature have more iron than sulfur. (Data are from references 24-30, 34, 48—51, 55-57, 59-61, 71, 104, 112, 199, 205, 222, and 223.)...

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See also in sourсe #XX -- [ Pg.300 ]

See also in sourсe #XX -- [ Pg.300 ]




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