TABLE 16

REAGENTS REQUIRED IN LIME AND SODA PROCESS

FOR TREATING 1000 U. S. GALLONS OF WATER

PER GRAIN PER GALLON OF CONTAINED IMPURITIES[16]

+-----------------------+-----------+-----------+

| | Lime[17] | Soda[18] |

| | Pounds | Pounds |

+-----------------------+-----------+-----------+

| Calcium Carbonate | 0.098 | ... |

| Calcium Sulphate | ... | 0.124 |

| Calcium Chloride | ... | 0.151 |

| Calcium Nitrate | ... | 0.104 |

| Magnesium Carbonate | 0.234 | ... |

| Magnesium Sulphate | 0.079 | 0.141 |

| Magnesium Chloride | 0.103 | 0.177 |

| Magnesium Nitrate | 0.067 | 0.115 |

| Ferrous Carbonate | 0.169 | ... |

| Ferrous Sulphate | 0.070 | 0.110 |

| Ferric Sulphate | 0.074 | 0.126 |

| Aluminum Sulphate | 0.087 | 0.147 |

| Free Sulphuric Acid | 0.100 | 0.171 |

| Sodium Carbonate | 0.093 | ... |

| Free Carbon Dioxide | 0.223 | ... |

| Hydrogen Sulphite | 0.288 | ... |

+-----------------------+-----------+-----------+

The chemicals used in the ordinary lime and soda process of feed water

treatment are common lime and soda. The efficiency of such apparatus

will depend wholly upon the amount and character of the impurities in

the water to be treated. Table 16 gives the amount of lime and soda

required per 1000 gallons for each grain per gallon of the various

impurities found in the water. This table is based on lime containing 90

per cent calcium oxide and soda containing 58 per cent sodium oxide,

which correspond to the commercial quality ordinarily purchasable. From

this table and the cost of the lime and soda, the cost of treating any

water per 1000 gallons may be readily computed.

Less Usual Reagents--Barium hydrate is sometimes used to reduce

permanent hardness or the calcium sulphate component. Until recently,

the high cost of barium hydrate has rendered its use prohibitive but at

the present it is obtained as a by-product in cement manufacture and it

may be purchased at a more reasonable figure than heretofore. It acts

directly on the soluble sulphates to form barium sulphate which is

insoluble and may be precipitated. Where this reagent is used, it is

desirable that the reaction be allowed to take place outside of the

boiler, though there are certain cases where its internal use is

permissible.

Barium carbonate is sometimes used in removing calcium sulphate, the

products of the reaction being barium sulphate and calcium carbonate,

both of which are insoluble and may be precipitated. As barium carbonate

in itself is insoluble, it cannot be added to water as a solution and

its use should, therefore, be confined to treatment outside of the

boiler.

Silicate of soda will precipitate calcium carbonate with the formation

of a gelatinous silicate of lime and carbonate of soda. If calcium

sulphate is also present, carbonate of soda is formed in the above

reaction, which in turn will break down the sulphate.

Oxalate of soda is an expensive but efficient reagent which forms a

precipitate of calcium oxalate of a particularly insoluble nature.

Alum and iron alum will act as efficient coagulents where organic matter

is present in the water. Iron alum has not only this property but also

that of reducing oil discharged from surface condensers to a condition

in which it may be readily removed by filtration.

Corrosion--Where there is a corrosive action because of the presence of

acid in the water or of oil containing fatty acids which will decompose

and cause pitting wherever the sludge can find a resting place, it may

be overcome by the neutralization of the water by carbonate of soda.

Such neutralization should be carried to the point where the water will

just turn red litmus paper blue. As a preventative of such action

arising from the presence of the oil, only the highest grades of

hydrocarbon oils should be used.

Acidity will occur where sea water is present in a boiler. There is the

possibility of such an occurrence in marine practice and in stationary

plants using sea water for condensing, due to leaky condenser tubes,

priming in the evaporators, etc. Such acidity is caused through the

dissociation of magnesium chloride into hydrochloride acid and magnesia

under high temperatures. The acid in contact with the metal forms an

iron salt which immediately upon its formation is neutralized by the

free magnesia in the water, thereby precipitating iron oxide and

reforming magnesium chloride. The preventive for corrosion arising from

such acidity is the keeping tight of the condenser. Where it is

unavoidable that some sea water should find its way into a boiler, the

acidity resulting should be neutralized by soda ash. This will convert

the magnesium chloride into magnesium carbonate and sodium chloride,

neither of which is corrosive but both of which are scale-forming.

The presence of air in the feed water which is sucked in by the feed

pump is a well recognized cause of corrosion. Air bubbles form below the

water line and attack the metal of the boiler, the oxygen of the air

causing oxidization of the boiler metal and the formation of rust. The

particle of rust thus formed is swept away by the circulation or is

dislodged by expansion and the minute pit thus left forms an ideal

resting place for other air bubbles and the continuation of the

oxidization process. The prevention is, of course, the removing of the

air from the feed water. In marine practice, where there has been

experienced the most difficulty from this source, it has been found to

be advantageous to pump the water from the hot well to a filter tank

placed above the feed pump suction valves. In this way the air is

liberated from the surface of the tank and a head is assured for the

suction end of the pump. In this same class of work, the corrosive

action of air is reduced by introducing the feed through a spray nozzle

into the steam space above the water line.

Galvanic action, resulting in the eating away of the boiler metal

through electrolysis was formerly considered practically the sole cause

of corrosion. But little is known of such action aside from the fact

that it does take place in certain instances. The means adopted as a

remedy is usually the installation of zinc plates within the boiler,

which must have positive metallic contact with the boiler metal. In this

way, local electrolytic effects are overcome by a still greater

electrolytic action at the expense of the more positive zinc. The

positive contact necessary is difficult to maintain and it is

questionable just what efficacy such plates have except for a short

period after their installation when the contact is known to be

positive. Aside from protection from such electrolytic action, however,

the zinc plates have a distinct use where there is the liability of air

in the feed, as they offer a substance much more readily oxidized by

such air than the metal of the boiler.

Foaming--Where foaming is caused by organic matter in suspension, it may

be largely overcome by filtration or by the use of a coagulent in

connection with filtration, the latter combination having come recently

into considerable favor. Alum, or potash alum, and iron alum, which in

reality contains no alumina and should rather be called potassia-ferric,

are the coagulents generally used in connection with filtration. Such

matter as is not removed by filtration may, under certain conditions, be

handled by surface blowing. In some instances, settling tanks are used

for the removal of matter in suspension, but where large quantities of

water are required, filtration is ordinarily substituted on account of

the time element and the large area necessary in settling tanks.

Where foaming occurs as the result of overtreatment of the feed water,

the obvious remedy is a change in such treatment.

Priming--Where priming is caused by excessive concentration of salts

within a boiler, it may be overcome largely by frequent blowing down.

The degree of concentration allowable before priming will take place

varies widely with conditions of operation and may be definitely

determined only by experience with each individual set of conditions. It

is the presence of the salts that cause priming that may result in the

absolute unfitness of water for boiler feed purposes. Where these salts

exist in such quantities that the amount of blowing down necessary to

keep the degree of concentration below the priming point results in

excessive losses, the only remedy is the securing of another supply of

feed, and the results will warrant the change almost regardless of the

expense. In some few instances, the impurities may be taken care of by

some method of water treatment but such water should be submitted to an

authority on the subject before any treatment apparatus is installed.

[Illustration: 3000 Horse-power Installation of Cross Drum Babcock &

Wilcox Boilers and Superheaters Equipped with Babcock & Wilcox Chain

Grate Stokers at the Washington Terminal Co., Washington, D. C.]

Boiler Compounds--The method of treatment of feed water by far the most

generally used is by the use of some of the so-called boiler compounds.

There are many reliable concerns handling such compounds who

unquestionably secure the promised results, but there is a great

tendency toward looking on the compound as a "cure all" for any water

difficulties and care should be taken to deal only with reputable

concerns.

The composition of these compounds is almost invariably based on soda

with certain tannic substances and in some instances a gelatinous

substance which is presumed to encircle scale particles and prevent

their adhering to the boiler surfaces. The action of these compounds is

ordinarily to reduce the calcium sulphate in the water by means of

carbonate of soda and to precipitate it as a muddy form of calcium

carbonate which may be blown off. The tannic compounds are used in

connection with the soda with the idea of introducing organic matter

into any scale already formed. When it has penetrated to the boiler

metal, decomposition of the scale sets in, causing a disruptive effect

which breaks the scale from the metal sometimes in large slabs. It is

this effect of boiler compounds that is to be most carefully guarded

against or inevitable trouble will result from the presence of loose

scale with the consequent danger of tube losses through burning.

When proper care is taken to suit the compound to the water in use, the

results secured are fairly effective. In general, however, the use of

compounds may only be recommended for the prevention of scale rather

than with the view to removing scale which has already formed, that is,

the compounds should be introduced with the feed water only when the

boiler has been thoroughly cleaned.

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