Steam corrosion

The explicit aims of boiler and feed-water treatment are to minimise corrosion, deposit formation, and carryover of boiler water solutes in steam. Corrosion control is sought primarily by adjustment of the pH and dissolved oxygen concentrations. Thus, the cathodic half-cell reactions of the two common corrosion processes are hindered. The pH is brought to a compromise value, usually just above 9 (at 25°C), so that the tendency for metal dissolution is at a practical minimum for both steel and copper alloys. Similarly, by the removal of dissolved oxygen, by a combination of mechanical and chemical means, the scope for the reduction of oxygen to hydroxyl is severely constrained. 

Condensate contamination originates from several sources, including BW carryover into the generated steam, corrosion debris pickup... 

Problems with steam can occur in let-down valves as a result of erosion-corrosion. To prevent attack, hard facing (e.g., stellite) is commonly used when the pressure drop exceeds 150 to 200 psi (1,035 to 1,380 kPa). This limit can be raised to 500 psi (3,450 kPa) for clean, dry steam. Corrosion-erosion also occurs in wet steam. Carbon steel is unsatisfactory in wet steam when pvx, the product of the pressure (psia), velocity (ft/s), and wetness (% water) exceeds 1 x 105. Resistance to wet steam is enhanced by increasing both the metal hardness and chromium content. 

W.L. Williams, Chloride and caustic stress corrosion of austenitic stainless steel in hot water and steam. Corrosion 13 (1957) 539t—545t. 

Balanced pressure, thermostatic operating principle = vapor pressure of fluid inside bellows. Not for superheated steam, corrosive condensate or waterhammer. 

General service, blow-down service, hquids, gases, steam, corrosives, abrasive media, slurries... 

Figure 8.16 Type 321 stainless Steel expansion joint in 2.8 MPa (400 psi) steam service cracked from caustic carryover in the steam. Corrosion Basics An Introduction, 2nd edn., NACE International, by permission)...

Speidel M O, Denk J and Scarlin B 1991 Stress Corrosion Craoking and Corrosion Fatigue of Steam-Turbine Rotor and Blade Materials (Luxembourg Commission of the European Communities)... 

Benzylatnine. Warm an alcoholic suspension of 118-5 g. of finely-powdered benzyl phthalimide with 25 g. of 100 per cent, hydrazine hydrate (CAUTION corrosive liquid) a white, gelatinous precipitate is produced rapidly. Decompose the latter (when its formation appears complete) by heating with excess of hydrochloric acid on a steam bath. Collect the phthalyl hydrazide which separates by suction filtration, and wash it with a little water. Concentrate the filtrate by distillation to remove alcohol, cool, filter from the small amount of precipitated phthalyl hydrazide, render alkaline with excess of sodium hydroxide solution, and extract the liberated benzylamine with ether. Dry the ethereal solution with potassium hydroxide pellets, remove the solvent (compare Fig. //, 13, 4) on a water bath and finally distil the residue. Collect the benzylamine at 185-187° the 3ueld is 50 g. 

Recovery of Ammonia. The filter Hquor contains unreacted sodium chloride and substantially all the ammonia with which the brine was originally saturated. The ammonia may be fixed or free. Fixed ammonia (ammonium chloride [12125-02-97]) corresponds stoichiometrically to the precipitated sodium bicarbonate. Free ammonia includes salts such as ammonium hydroxide, bicarbonate, and carbonate, and the several possible carbon—ammonia compounds that decompose at moderate temperatures. A sulfide solution may be added to the filter Hquor for corrosion protection. The sulfide is distilled for eventual absorption by the brine in the absorber. As the filter Hquor enters the distiller, it is preheated by indirect contact with departing gases. The warmed Hquor enters the main coke, tile, or bubble cap-fiUed sections of the distiller where heat decomposes the free ammonium compounds and steam strips the ammonia and carbon dioxide from the solution. 

A.m blent Environment. The environment around the flow conduit must be considered in meter selection. Such factors as the ambient temperature and humidity, the pipe shock and vibration levels, the avadabiHty of electric power, and the corrosive and explosive characteristics of the environment may all influence flow meter selection. Special factors such as possible accidental flooding, the need for hosedown or steam cleaning, and the possibiHty of lightning or power transients may also need to be evaluated. 

In this pyrolysis, sub atmospheric partial pressures are achieved by employing a diluent such as steam. Because of the corrosive nature of the acids (HE and HCl) formed, the reactor design should include a platinum-lined tubular reactor made of nickel to allow atmospheric pressure reactions to be mn in the presence of a diluent. Because the pyrolysate contains numerous by-products that adversely affect polymerization, the TFE must be purified. Refinement of TFE is an extremely complex process, which contributes to the high cost of the monomer. Inhibitors are added to the purified monomer to avoid polymerization during storage terpenes such as t7-limonene and terpene B are effective (10). 

Chromium is the most effective addition to improve the resistance of steels to corrosion and oxidation at elevated temperatures, and the chromium—molybdenum steels are an important class of alloys for use in steam (qv) power plants, petroleum (qv) refineries, and chemical-process equipment. The chromium content in these steels varies from 0.5 to 10%. As a group, the low carbon chromium—molybdenum steels have similar creep—mpture strengths, regardless of the chromium content, but corrosion and oxidation resistance increase progressively with chromium content. 

Cobalt aHoys may find appHcation ia a fluidized-bed process for the direct combustion of coal (qv). CoCrAlY-coated Haynes 188 has proven to be one of the most resistant materials to a fireside corrosion process encountered ia tubes coimected the fluidized-bed combustor to a steam turbiae. 

Allowing DRI to become wet does not necessatily cause it to overheat. When large pdes of DRI are wetted with rain, the corrosion reactions are limited to the outer surface area of the pde and the resultant heat from the corrosion reactions is dissipated into the atmosphere. However, if water penetrates into the pde from the bottom, or if wet DRI is covered with dry DRI, the heat from corrosion reactions can budd up inside the pde to the point where rapid reoxidation begins. Corrosion occurs significantly faster with salt water than with fresh water. DRI saturated with water can cause steam explosions if it is batch charged into an electric arc furnace. 

Maleic Anhydride. The ACGIH threshold limit value in air for maleic anhydride is 0.25 ppm and the OSHA permissible exposure level (PEL) is also 0.25 ppm (181). Maleic anhydride is a corrosive irritant to eyes, skin, and mucous membranes. Pulmonary edema (collection of fluid in the lungs) can result from airborne exposure. Skin contact should be avoided by the use of mbber gloves. Dust respirators should be used when maleic anhydride dust is present. Maleic anhydride is combustible when exposed to heat or flame and can react vigorously on contact with oxidizers. The material reacts exothermically with water or steam. Violent decompositions of maleic anhydride can be catalyzed at high temperature by strong bases (sodium hydroxide, potassium hydroxide, calcium hydroxide, alkaU metals, and amines). Precaution should be taken during the manufacture and use of maleic anhydride to minimize the presence of basic materials. 

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