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Steam, Its Generation and Use · Babcock & Wilcox Company — chapter 30 of 70 · ~1,270 words · public domain

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The heat lost in the flue gases is L = 0.24 W (T - t) (15)

Where L = B. t. u. lost per pound of fuel, W = weight of flue gases in pounds per pound of dry coal, T = temperature of flue gases, t = temperature of atmosphere, 0.24 = specific heat of the flue gases.

The weight of flue gases, W, per pound of carbon can be computed directly from the flue gas analysis from the formula:

11 CO{2} + 8 O + 7 (CO + N) ---------------------------- (16) 3 (CO{2} + CO)

where CO_{2}, O, CO, and N are the percentages by volume as determined by the flue gas analysis of carbon dioxide, oxygen, carbon monoxide and nitrogen.

The weight of flue gas per pound of dry coal will be the weight determined by this formula multiplied by the percentage of carbon in the coal from an ultimate analysis.

Fig. 20. Loss Due to Heat Carried Away by Chimney Gases for Varying Percentages of Carbon Dioxide. Based on Boiler Room Temperature = 80 Degrees Fahrenheit. Nitrogen in Flue Gas = 80.5 Per Cent. Carbon Monoxide in Flue Gas = 0. Per Cent]

Fig. 20 represents graphically the loss due to heat carried away by dry chimney gases for varying percentages of CO_{2}, and different temperatures of exit gases.

The heat lost, due to the fact that the carbon in the fuel is not completely burned and carbon monoxide is present in the flue gases, in B. t. u. per pound of fuel burned is:

( CO ) L' = 10,150 × (-----------) (17) (CO + CO_{2})

where, as before, CO and CO_{2} are the percentages by volume in the flue gases and C is the proportion by weight of carbon which is burned and passes up the stack.

Fig. 21 represents graphically the loss due to such carbon in the fuel as is not completely burned but escapes up the stack in the form of carbon monoxide.

Fig. 21. Loss Due to Unconsumed Carbon Contained in the CO in the Flue Gases]

Apparatus for Flue Gas Analysis--The Orsat apparatus, illustrated in Fig. 22, is generally used for analyzing flue gases. The burette A is graduated in cubic centimeters up to 100, and is surrounded by a water jacket to prevent any change in temperature from affecting the density of the gas being analyzed.

For accurate work it is advisable to use four pipettes, B, C, D, E, the first containing a solution of caustic potash for the absorption of carbon dioxide, the second an alkaline solution of pyrogallol for the absorption of oxygen, and the remaining two an acid solution of cuprous chloride for absorbing the carbon monoxide. Each pipette contains a number of glass tubes, to which some of the solution clings, thus facilitating the absorption of the gas. In the pipettes D and E, copper wire is placed in these tubes to re-energize the solution as it becomes weakened. The rear half of each pipette is fitted with a rubber bag, one of which is shown at K, to protect the solution from the action of the air. The solution in each pipette should be drawn up to the mark on the capillary tube.

The gas is drawn into the burette through the U-tube H, which is filled with spun glass, or similar material, to clean the gas. To discharge any air or gas in the apparatus, the cock G is opened to the air and the bottle F is raised until the water in the burette reaches the 100 cubic centimeters mark. The cock G is then turned so as to close the air opening and allow gas to be drawn through H, the bottle F being lowered for this purpose. The gas is drawn into the burette to a point below the zero mark, the cock G then being opened to the air and the excess gas expelled until the level of the water in F and in A are at the zero mark. This operation is necessary in order to obtain the zero reading at atmospheric pressure.

The apparatus should be carefully tested for leakage as well as all connections leading thereto. Simple tests can be made; for example: If after the cock G is closed, the bottle F is placed on top of the frame for a short time and again brought to the zero mark, the level of the water in A is above the zero mark, a leak is indicated.

Before taking a final sample for analysis, the burette A should be filled with gas and emptied once or twice, to make sure that all the apparatus is filled with the new gas. The cock G is then closed and the cock I in the pipette B is opened and the gas driven over into B by raising the bottle F. The gas is drawn back into A by lowering F and when the solution in B has reached the mark in the capillary tube, the cock I is closed and a reading is taken on the burette, the level of the water in the bottle F being brought to the same level as the water in A. The operation is repeated until a constant reading is obtained, the number of cubic centimeters being the percentage of CO_{2} in the flue gases.

The gas is then driven over into the pipette C and a similar operation is carried out. The difference between the resulting reading and the first reading gives the percentage of oxygen in the flue gases.

The next operation is to drive the gas into the pipette D, the gas being given a final wash in E, and then passed into the pipette C to neutralize any hydrochloric acid fumes which may have been given off by the cuprous chloride solution, which, especially if it be old, may give off such fumes, thus increasing the volume of the gases and making the reading on the burette less than the true amount.

The process must be carried out in the order named, as the pyrogallol solution will also absorb carbon dioxide, while the cuprous chloride solution will also absorb oxygen.

As the pressure of the gases in the flue is less than the atmospheric pressure, they will not of themselves flow through the pipe connecting the flue to the apparatus. The gas may be drawn into the pipe in the way already described for filling the apparatus, but this is a tedious method. For rapid work a rubber bulb aspirator connected to the air outlet of the cock G will enable a new supply of gas to be drawn into the pipe, the apparatus then being filled as already described. Another form of aspirator draws the gas from the flue in a constant stream, thus insuring a fresh supply for each sample.

The analysis made by the Orsat apparatus is volumetric; if the analysis by weight is required, it can be found from the volumetric analysis as follows:

Multiply the percentages by volume by either the densities or the molecular weight of each gas, and divide the products by the sum of all the products; the quotients will be the percentages by weight. For most work sufficient accuracy is secured by using the even values of the molecular weights.

The even values of the molecular weights of the gases appearing in an analysis by an Orsat are:

Carbon Dioxide 44 Carbon Monoxide 28 Oxygen 32 Nitrogen 28

Table 33 indicates the method of converting a volumetric flue gas analysis into an analysis by weight.

TABLE 33

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