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EPPWT Handout
EPPWT Handout
Water Impurities Water impurities include dissolved and suspended solids. Calcium bicarbonate is a soluble salt. A solution of calcium bicarbonate is clear, because the calcium and bicarbonate are present as atomic sized ions which are not large enough to reflect light. Some soluble minerals impart a color to the solution. Soluble iron salts produce pale yellow or green solutions; some copper salts form intensely blue solutions. Although colored, these solutions are clear. Suspended solids are substances that are not completely soluble in water and are present as particles. These particles usually impart a visible turbidity to the water. Dissolved and suspended solids are present in most surface waters. Seawater is very high in soluble sodium chloride; suspended sand and silt make it slightly cloudy. An extensive list of soluble and suspended impurities found in water is given in Table 1-1. Table 1-1. Common impurities found in fresh water. Constituent Chemical Formula Difficulties Caused
imparts unsightly appearance to water; deposits in water lines, process equipment, etc.; interferes with most process uses chief source of scale in heat exchange equipment, boilers, pipe lines, etc.; forms curds with soap, interferes with dyeing, etc. foam and carryover of solids with steam; embrittlement of boiler steel; bicarbonate and carbonate produce CO2 in steam, a source of corrosion in condensate lines corrosion corrosion in water lines, particularly steam and condensate lines ion pH varies according to acidic or alkaline solids in water; most natural waters have a pH of 6.0-8.0
Means of Treatment
Turbidity
in
settling,
Hardness
Alkalinity
lime and lime-soda softening; acid treatment; hydrogen zeolite softening; demineralization dealkalization by anion exchange neutralization alkalies with
CO2
aeration, deaeration, neutralization with alkalies pH can be increased by alkalies and decreased by acids
pH
Sulfate
SO42-
Chloride
Cl
Nitrate
NO3
Fluoride
F-
Sodium
Na
Silica
SiO2
Iron
Manganese
Mn2+
Aluminum
AI3+
Oxygen
O2
Hydrogen Sulfide
H2 S
aeration; chlorination; highly basic anion exchange cation exchange with hydrogen zeolite; chlorination; deaeration
Ammonia
NH3
Dissolved Solids
none
lime softening and cation exchange by hydrogen zeolite; demineralization, reverse osmosis, electrodialysis, evaporation
Suspended Solids
none
Total Solids
none
Surface Water The ultimate course of rain or melting snow depends on the nature of the terrain over which it flows. In areas consisting of hard packed clay, very little water penetrates the ground. In these cases, the water generates "runoff". The runoff collects in streams and rivers. The rivers empty into bays and estuaries, and the water ultimately returns to the sea, completing one major phase of the hydrologic cycle of the nature. As water runs off along the surface, it stirs up and suspends particles of sand and soil, creating silt in the surface water. In addition, the streaming action erodes rocky surfaces, producing more sand. As the surface water cascades over rocks, it is aerated. The combination of oxygen, inorganic nutrients leached from the terrain, and sunlight supports a wide variety of life forms in the water, including algae, fungi, bacteria, small crustaceans, and fish. Often, river beds are lined with trees, and drainage areas feeding the rivers are forested. Leaves and pine needles constitute a large percentage of the biological content of the water. After it dissolves in the water, this material becomes a major cause of fouling of ion exchange resin used in water treatment.
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In contrast to surface supplies, ground waters are relatively free from suspended contaminants, because they are filtered as they move through the strata. The filtration also removes most of the biological contamination. Some ground waters with a high iron content contain sulfate reducing bacteria. These are a source of fouling and corrosion in industrial water systems. Groundwater chemistry tends to be very stable over time. A groundwater may contain an undesirable level of scale forming solids, but due to its fairly consistent chemistry it may be treated effectively. Mineral Reactions: As groundwater encounters different minerals, it dissolves them according to their solubility characteristics. In some cases chemical reactions occur, enhancing mineral solubility. A good example is the reaction of groundwater with limestone. Water percolating from the surface contains atmospheric gases. One of these gases is carbon dioxide, which forms carbonic acid when dissolved in water. The decomposition of organic matter beneath the surface is another source of carbon dioxide. Limestone is a mixture of calcium and magnesium carbonate. The mineral, which is basic, is only slightly soluble in neutral water. The slightly acidic groundwater reacts with basic limestone in a neutralization reaction that forms a salt and a water of neutralization. The salt formed by the reaction is a mixture of calcium and magnesium bicarbonate. Both bicarbonates are quite soluble. This reaction is the source of the most common deposition and corrosion problems faced by industrial users. The calcium and
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scale that crystallized directly onto tube surfaces sludge deposits that precipitated elsewhere and were transported to the metal surface by the flowing water
Scale is formed by salts that have limited solubility but are not totally insoluble in boiler water. These salts reach the deposit site in a soluble form and precipitate when concentrated by evaporation. The precipitates formed usually have a fairly homogeneous composition and crystal structure. High heat transfer rates cause high evaporation rates, which concentrate the remaining water in the area of evaporation. A number of different scale-forming compounds can precipitate from the concentrated water. The nature of the scale formed depends on the chemical composition of the concentrated water. Normal deposit constituents are calcium, magnesium, silica, aluminum, iron, and (in some cases) sodium. The exact combinations in which they exist vary from boiler to boiler, and from location to location within a boiler (Table 1- 3). Scale may form as calcium silicate in one boiler and as sodium iron silicate in another. Compared to some other precipitation reactions, such as the formation of calcium phosphate, the crystallization of scale is a slow process. As a result, the crystals formed are well defined, and a hard, dense, and highly insulating material is formed on the tube metal. Some forms of scale are so tenacious that they resist any type of removal-mechanical or chemical. Sludge is the accumulation of solids that precipitate in the bulk boiler water or enter the boiler as suspended solids. Sludge deposits can be hard, dense, and tenacious. When exposed to high heat levels (e.g., when a boiler is drained hot), sludge deposits are often baked in place. Sludge deposits hardened in this way can be as troublesome as scale. Once deposition starts, particles present in the circulating water can become bound to the deposit. Intraparticle binding does not need to occur between every particle in a deposit mass. Some nonbound particles can be captured in a network of bound particles.
Table 1- 3. Crystalline scale constituents identified by X-ray diffraction. Name Acmite Analcite Anhydrite Aragonite Brucite Calcite Cancrinite Hematite Hydroxyapatite Magnetite Pectolite Quartz Serpentine Thenardite Wallastonite Xonotlite Formula Na2OFe2O34SiO2 Na2OAl2O34SiO22H2O CaSO4 CaCO3 Mg(OH)2 CaCO3 4Na2OCaO4Al2O32CO29SiO23H2O Fe2O3 Ca10(OH)2(PO4)6 Fe3O4 Na2O4CaO6SiO2H2O SiO2 3MgO2SiO22H2O Na2SO4 CaSiO3 5CaO5SiO2H2O
Binding is often a function of surface charge and loss of water of hydration. Iron oxide, which exists in many hydrated and oxide forms, is particularly prone to bonding. Some silicates will do the same, and many oil contaminants are notorious deposit binders, due to polymerization and degradation reactions. Since these scale components have the small thermal conductivities as shown in Table below, the scale adhesion on the heating surface remarkably reduces the thermal efficiency of boiler. Substance Silica scale Calcium carbonate scale Calcium sulfate scale Calcium phosphate scale Iron oxide (hematite) scale Iron oxide (magnetite) scale Carbon steel Copper Thermal conductivity (kcal/mhC) 0.20.4 0.40.6 0.52.0 0.50.7 35 1 4060 320360
Figure in the right shows the relationship between the temperature and the allowable tensile stresses of carbon steels using as boiler tubes. When the temperature exceeds 350 C, the allowable stress starts to decrease and reaches the 50 to 60% of the original value at 450 C. Therefore, the tube wall temperature should be kept below 450C for the safe boiler operation and the scale thickness on the tube has to be controlled thinner STB 410 is equivalent of ASTM grade SA210 GR A1 than 1 to 2 mm as shown in JIS JIS STB 340 is equivalent of ASTM grade SA 192 previous Figure. In addition to causing material damage by insulating the heat transfer path from the boiler flame to the water 9
They roughen the tube surface and increase the drag coefficient in the boiler circuit. Reduced circulation in a generating tube contributes to accelerated deposition, overheating, and premature steam-water separation.
BOILER CIRCULATION Figures below illustrate the process of boiler circulation and how scaling may affect it. The left legs of the U-tubes represent downcomers and are filled with relatively cool water. The right legs represent generating tubes and are heated. The heat generates steam bubbles, and convection currents create circulation. As more heat is applied, more steam is generated and the circulation rate increases. If deposits form (Figure right), the roughened surface and partially restricted opening resist flow, reducing circulation. At a constant heat input the same amount of steam is generated, so the steamwater ratio in the generating tube is increased. The water in the tube becomes more concentrated, increasing the potential for deposition of boiler water salts. In extreme cases, deposition becomes heavy enough to reduce circulation to a point at which premature steam-water separation occurs. When this happens in a furnace tube, failure due to overheating is rapid. When deposits are light they may not cause tube failures, but they reduce any safety margin in the boiler design. Up to the point of premature steam-water separation, the circulation rate of a boiler is increased with increased heat input. When the circuit is dirty, the inflection point of the circulation-to-heat input curve moves to the left, and the overall water circulation is reduced. This is represented by the lower broken line. Circulation and deposition are closely related. If the surface charge on a particle is relatively neutral in its tendency to cause the particle either to adhere to the tube wall or to remain suspended, an adequate water sweep will keep it off the tube. If the circulation through a circuit is not adequate to provide sufficient water sweep, the neutral particle may adhere to the tube. In cases of extremely low circulation, total evaporation can occur and normally soluble sodium salts deposit.
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maintenance of proper pH and alkalinity levels control of oxygen and boiler feedwater contamination reduction of mechanical stresses operation pressure within design specifications, especially for temperature and
proper precautions during start-up and shutdown effective monitoring and control
Corrosion Tendencies of Boiler System Components Most industrial boiler and feedwater systems are constructed of carbon steel. Many have copper alloy and/or stainless steel feedwater heaters and condensers. Some have stainless steel superheater elements. Proper treatment of boiler feedwater effectively protects against corrosion of feedwater heaters, economizers, and deaerators. The ASME Consensus for Industrial Boilers specifies maximum levels of contaminants for corrosion and deposition control in boiler systems. The consensus is that feedwater oxygen, iron, and copper content should be very low (e.g., less than 7 ppb oxygen, 20 ppb iron, and 15 ppb copper for a 900 psig boiler) and that pH should be maintained between 8.5 and 9.5 for system corrosion protection. In order to minimize boiler system corrosion, an understanding of the operational requirements for all critical system components is necessary. Deaerators Deaerators are used to heat feedwater and reduce oxygen and other dissolved gases to acceptable levels. Corrosion fatigue at or near welds is a major problem in deaerators. Most corrosion fatigue cracking has been reported to be the result of mechanical factors, such as manufacturing procedures, poor welds, and lack of stress-relieved welds. Operational problems such as water/steam hammer can also be a factor.
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regular monitoring of operation minimization of stresses during start-up maintenance of stable temperature and pressure levels control of dissolved oxygen and pH in the feedwater regular out-of-service inspection using established nondestructive techniques
Other forms of corrosive attack in deaerators include stress corrosion cracking of the stainless steel tray chamber, inlet spray valve spring cracking, corrosion of vent condensers due to oxygen pitting, and erosion of the impingement baffles near the steam inlet connection. Economizers Economizer corrosion control involves procedures similar to those employed for protecting feedwater heaters. Economizers help to improve boiler efficiency by extracting heat from flue gases discharged from the fireside of a boiler. Economizers can be classified as nonsteaming or steaming. In a steaming economizer, 5-20% of the incoming feedwater becomes steam. Steaming economizers are particularly sensitive to deposition from feedwater contaminants and resultant under-deposit corrosion. Erosion at tube bends is also a problem in steaming economizers. Oxygen pitting, caused by the presence of oxygen and temperature increase, is a major problem in economizers; therefore, it is necessary to maintain essentially oxygen-free water in these units. The inlet is subject to severe pitting, because it is often the first area after the deaerator to be exposed to increased heat. Whenever possible, tubes in this area should be inspected closely for evidence of corrosion. Economizer heat transfer surfaces are subject to corrosion product buildup and deposition of incoming metal oxides. These deposits can slough off during operational load and chemical changes. Corrosion can also occur on the gas side of the economizer due to contaminants in the flue gas, forming low-pH compounds. Generally, economizers are arranged for downward flow of gas and upward flow of water. Tubes that form the heating surface may be smooth or provided with extended surfaces. Superheaters Superheater corrosion problems are caused by a number of mechanical and chemical conditions. One major problem is the oxidation of superheater metal due to high gas temperatures, usually occurring during transition periods, such as start-up and shutdown. Deposits due to carryover can contribute to the problem. Resulting failures usually occur in the bottom loops-the hottest areas of the superheater tubes. Oxygen pitting, particularly in the pendant loop area, is another major corrosion problem in superheaters. It is caused when water is exposed to oxygen during downtime. Close temperature control helps to minimize this problem. In addition, a nitrogen blanket and chemical oxygen scavenger can be used to maintain oxygenfree conditions during downtime. Low-Pressure Steam and Hot Water Heating Systems Hot water boilers heat and circulate water at approximately 200F. Steam heating boilers are used to generate steam at low pressures, such as 15 psig. Generally,
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scratches in a metal surface differential stresses in a metal differences in temperature conductive deposits
Pitting of boiler tube banks has been encountered due to metallic copper deposits. Such deposits may form during acid cleaning procedures if the procedures do not completely compensate for the amount of copper oxides in the deposits or if a copper removal step is not included. Dissolved copper may be plated out on freshly cleaned surfaces, establishing anodic corrosion areas and forming pits, which are very similar to oxygen pits in form and appearance. This process is illustrated by the following reactions involving hydrochloric acid as the cleaning solvent. Magnetite is dissolved and yields an acid solution containing both ferrous (Fe+) and ferric (Fe+) chlorides (ferric chlorides are very corrosive to steel and copper) Fe3O4 + 8HCl FeCl2 + 2FeCl3 + 4H2O
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Once cuprous chloride is in solution, it is immediately redeposited as metallic copper on the steel surface according to the following reaction: 2CuCl + Fe FeCl2 + 2Cu0
Thus, hydrochloric acid cleaning can cause galvanic corrosion unless the copper is prevented from plating on the steel surface. A complexing agent is added to prevent the copper from redepositing. The following chemical reaction results: FeCl3 + Cu + Complexing Agent FeCl2 + CuCl
This can take place as a separate step or during acid cleaning. Both iron and the copper are removed from the boiler, and the boiler surfaces can then be passivated. In most cases, the copper is localized in certain tube banks and causes random pitting. When deposits contain large quantities of copper oxide or metallic copper, special precautions are required to prevent the plating out of copper during cleaning operations. Caustic Corrosion Concentration of caustic (NaOH) can occur either as a result of steam blanketing (which allows salts to concentrate on boiler metal surfaces) or by localized boiling beneath porous deposits on tube surfaces. Caustic corrosion (gouging) occurs when caustic is concentrated and dissolves the protective magnetite (Fe3O4 ) layer. Iron, in contact with the boiler water, forms magnetite and the protective layer is continuously restored. However, as long as a high caustic concentration exists, the magnetite is constantly dissolved, causing a loss of base metal and eventual failure. Steam blanketing is a condition that occurs when a steam layer forms between the boiler water and the tube wall. Under this condition, insufficient water reaches the tube surface for efficient heat transfer. The water that does reach the overheated boiler wall is rapidly vaporized, leaving behind a concentrated caustic solution, which is corrosive. Porous metal oxide deposits also permit the development of high boiler water concentrations. Water flows into the deposit and heat applied to the tube causes the water to evaporate, leaving a very concentrated solution. Again, corrosion may occur. Caustic attack creates irregular patterns, often referred to as gouges. Deposition may or may not be found in the affected area. Boiler feedwater systems using demineralized or evaporated makeup or pure condensate may be protected from caustic attack through coordinated phosphate/pH control. Phosphate buffers the boiler water, reducing the chance of large pH changes due to the development of high caustic concentrations. Excess caustic combines with disodium phosphate and forms trisodium phosphate. Sufficient disodium phosphate must be available to combine with all of the free caustic in order to form trisodium phosphate.
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This results in the prevention of caustic buildup beneath deposits or within a crevice where leakage is occurring. Caustic corrosion and caustic embrittlement does not occur, because high caustic concentrations do not develop. Different forms of phosphate consume or add caustic as the phosphate shifts to the proper form. For example, addition of monosodium phosphate consumes caustic as it reacts with caustic to form disodium phosphate in the boiler water according to the following reaction: NaH2PO4 + NaOH Na2HPO4 + H2O
Conversely, addition of trisodium phosphate adds caustic, increasing boiler water pH: Na3PO4 + H2O Na2HPO4 + NaOH
Control is achieved through feed of the proper type of phosphate to either raise or lower the pH while maintaining the proper phosphate level. Increasing blowdown lowers both phosphate and pH. Therefore, various combinations and feed rates of phosphate, blowdown adjustment, and caustic addition are used to maintain proper phosphate/pH levels. Elevated temperatures at the boiler tube wall or deposits can result in some precipitation of phosphate. This effect, termed "phosphate hideout," usually occurs when loads increase. When the load is reduced, phosphate reappears. Clean boiler water surfaces reduce potential concentration sites for caustic. Deposit control treatment programs, such as those based on chelants and synthetic polymers, can help provide clean surfaces. Where steam blanketing is occurring, corrosion can take place even without the presence of caustic, due to the steam/magnetite reaction and the dissolution of magnetite. In such cases, operational changes or design modifications may be necessary to eliminate the cause of the problem. Acidic Corrosion Low makeup or feedwater pH can cause serious acid attack on metal surfaces in the preboiler and boiler system. Even if the original makeup or feedwater pH is not low, feedwater can become acidic from contamination of the system. Common causes include the following:
improper operation or control of demineralizer cation units process contamination of condensate (e.g., sugar contamination in food processing plants) cooling water contamination from condensers
Acid corrosion can also be caused by chemical cleaning operations. Overheating of the cleaning solution can cause breakdown of the inhibitor used, excessive exposure of metal to cleaning agent, and high cleaning agent concentration. Failure to neutralize acid solvents completely before start-up has also caused problems.
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