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Washed steel

Figure 2 Typical ISS apectral data obtained from routine depth profile of cleaned washed steel. Left spectrum represents surface. Right spectrum represents about 50-A depth. Expansiona ahown top left. Relative atomic compositions plotted top right. Figure 2 Typical ISS apectral data obtained from routine depth profile of cleaned washed steel. Left spectrum represents surface. Right spectrum represents about 50-A depth. Expansiona ahown top left. Relative atomic compositions plotted top right.
A flask filled with acid-washed steel wool is fitted with a long, thin glass tube in a rubber stopper. When the flask is inverted so the tube opening is in a beaker of colored water, the water slowly begins to rise in the tube. Write a summary of this experiment, as if you had performed it. Explain what makes the water rise. Predict what portion of the flask wiU be fiUed with water at the end of the experiment. [Pg.581]

The corrosion rate of steel in carbonic acid is faster than in hydrochloric acid Correlations are available to predict the rate of steel corrosion for different partial pressures of CO2 and different temperatures. At high temperatures the iron carbonate forms a film of protective scale on the steel s surface, but this is easily washed away at lower temperatures (again a corrosion nomogram is available to predict the impact of the scale on the corrosion rate at various CO2 partial pressures and temperatures). [Pg.94]

To prepare the hydrochloride, dissolve about 1 g. of the compound (which need not be perfectly dry) in about 8 ml. of alcohol. Add this solution to boiling dilute hydrochloric acid (10 ml. of the concentrated acid and 80 ml. of water). Boil for 5 minutes, filter the hot solution if necessary, and allow to cool. p-Amino-azobenzene hydrochloride separates in steel-blue crystals. Filter, wash with a little dilute hydrochloric acid, and dry. [Pg.627]

Pentaerythritol may be nitrated by a batch process at 15.25°C using concentrated nitric acid in a stainless steel vessel equipped with an agitator and cooling coils to keep the reaction temperature at 15—25°C. The PETN is precipitated in a jacketed diluter by adding sufficient water to the solution to reduce the acid concentration to about 30%. The crystals are vacuum filtered and washed with water followed by washes with water containing a small amount of sodium carbonate and then cold water. The water-wet PETN is dissolved in acetone containing a small amount of sodium carbonate at 50°C and reprecipitated with water the yield is about 95%. Impurities include pentaerythritol trinitrate, dipentaerythritol hexanitrate, and tripentaerythritol acetonitrate. Pentaerythritol tetranitrate is shipped wet in water—alcohol in packing similar to that used for primary explosives. [Pg.15]

Most manufacturing equipment should be made of stainless steel. The liming tanks, however, can be either concrete or wood (qv). Properly lined iron tanks are often used for the washing and acidification, ie, souring, operations. Most gelatin plants achieve efficient processes by operating around the clock. The product is tested in batches and again as blends to confirm conformance to customer specifications. [Pg.207]

For the production of tartar emetic (antimony potassium tartrate [28300-74-5]), potassium bitartrate [868-14 ] and antimony oxide, Sb202, are added simultaneously to water in a stainless-steel reactor. The reaction mixture is diluted, filtered, and collected in jacketed granulators where crystallization takes place after cooling. Centrihiging, washing, and drying complete the process. [Pg.526]

Mercury spills should be cleaned up immediately by use of a special vacuum cleaner. The area should then be washed with a dilute calcium sulfide solution. Small quantities of mercury can be picked up by mixing with copper metal granules or powder, or with zinc granules or powder. To avoid or minimize spills, some plants use steel trays as pallets so that a spih, whether of mercury or a mercury compound, is contained on the steel tray. [Pg.116]

A 95% yield of pure anthraquinone was obtained. This is an almost quantitative yield based on the 100% content of the anthracene used. The cmde anthraquinone was then purified. To a jacketed steel kettie, provided with an agitator, was added cmde anthraquinone and nitrobenzene. Under agitation, the charge was heated at 130—140°C until a complete solution resulted. Under slow agitation, the solution was cooled to 30 °C and the resulting slurry of anthraquinone was filtered on a pressure filter. The cake was washed twice with nitrobenzene, then was reslurried on the filter with nitrobenzene, sucked dry, and transferred to a vacuum dryer where the nitrobenzene was distilled. The dried anthraquinone was discharged to suitable containers. A 99% yield of pure anthraquinone was obtained equal to a recovery of approximately 90% based on the cmde anthraquinone. [Pg.421]

Although 600 m of water is used to make a metric ton of fertilizer, 150—240 m to make a tonne of steel, 480 m to make a tonne of gasoline, and 1000 m to make a tonne of acetate fiber, Htde if any is required chemically in any of these processes. Recycling can reduce industrial requirements by a factor of 10—50. Much of this water, particularly that for cooling, and often that for washing, can be saline. Some petroleum refiners have used salt water to remove heat (water s principal role in gasoline production), and some have actually produced table salt by evaporation in cooling towers. [Pg.238]

Microstrainers. Microstrainers are rotating steel screens with extremely fine stainless steel mesh (85—170 perforations per square centimeter (13—26/in. )). The flowing Hquid enters the open end of the dmm and passes through the mesh to the effluent end. The mesh traps soHd impurities and rotates with the dmm. A wash-water spray washes the trapped soHds into a hopper for final disposal. The mesh is washed with filtered effluent discharged from jets fitted into the dmm and then exposed to uv radiation to inhibit microbial growth. The mesh is washed with chlorine water at intervals of 7 to 28 days in order to control slime growth removal efficiencies are 30—55% of the appHed BOD and 40—60% of suspended soHds. [Pg.293]

At the end of the 72-h cycle, the cathodes are removed from the cells, washed in hot water, and the brittie deposit, 3—6 mm thick, is stripped by a series of air hammers. The metal is then cmshed by roUs to 50-mm size and again washed in hot water. The metal contains about 0.034% hydrogen and, after drying, is dehydrogenated by heating to at least 400°C in stainless steel cans. Composition limits for electrolytic chromium are shown in Table 4. [Pg.118]

Lime-Sulfuric. Recovery of citric acid by calcium salt precipitation is shown in Figure 3. Although the chemistry is straightforward, the engineering principles, separation techniques, and unit operations employed result in a complex commercial process. The fermentation broth, which has been separated from the insoluble biomass, is treated with a calcium hydroxide (lime) slurry to precipitate calcium citrate. After sufficient reaction time, the calcium citrate slurry is filtered and the filter cake washed free of soluble impurities. The clean calcium citrate cake is reslurried and acidified with sulfuric acid, converting the calcium citrate to soluble citric acid and insoluble calcium sulfate. Both the calcium citrate and calcium sulfate reactions are generally performed in agitated reaction vessels made of 316 stainless steel and filtered on commercially available filtration equipment. [Pg.183]

The wash primer is a special type of vinyl coating. This material contains a poly(vinyl butyral) resin, zinc chromate, and phosphoric acid in an alcohol-water solvent. The coating is so thin it is HteraUy washed onto a freshly blasted steel surface, where it passivates the metal surface by converting it to a thin iron phosphate-chromate coating. The alcohol solvent makes it possible to apply the coating over damp surfaces. The coating forms the first coat of... [Pg.365]

The tank house is divided into commercial and stripper sections. In the latter, one-day deposits are prepared by electrorefining anode copper onto oiled copper, stainless steel, or titanium blanks. These copper sheets are stripped from the blanks and fabricated into starter sheets for the commercial sections as starting cathodes. After 9—15 days, depending on the tank house, hill-term cathodes are pulled and washed and either sent to the casting department or sold direcdy. [Pg.202]


See other pages where Washed steel is mentioned: [Pg.387]    [Pg.455]    [Pg.387]    [Pg.455]    [Pg.275]    [Pg.850]    [Pg.507]    [Pg.185]    [Pg.873]    [Pg.891]    [Pg.385]    [Pg.67]    [Pg.10]    [Pg.92]    [Pg.348]    [Pg.390]    [Pg.398]    [Pg.173]    [Pg.153]    [Pg.268]    [Pg.289]    [Pg.361]    [Pg.101]    [Pg.432]    [Pg.131]    [Pg.249]    [Pg.421]    [Pg.291]    [Pg.413]    [Pg.499]    [Pg.13]    [Pg.154]    [Pg.462]    [Pg.417]    [Pg.366]    [Pg.353]    [Pg.367]   
See also in sourсe #XX -- [ Pg.387 ]




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Steel (continued washed

Wash table, stainless steel

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