Part 23

2.88 Al{2}O{3} + 1.83 Fe{2}O{3} + 1.36 FeO.

If this percentage of acid equivalent is less than that found by titration report the difference as percentage of free acid. If the percentage of acid equivalent is greater than that found by titration the difference divided by 2.88 is the percentage equivalent to the excess of aluminium oxide present. Divide this excess by the percentage of total aluminium oxide and report the quotient as the basicity ratio.

LIME.

Mix well the sample, which should contain no lumps. If foreign matter is present grind the sample to pass a 100–mesh sieve.

Place 20 grams of granulated cane sugar and 1 gram of the sample in a 250 cc. glass-stoppered bottle, tightly stopped, and mix the mass by rolling. Do not shake hard as much of the lime could thus be lost as dust. Then add 187.4 cc. of distilled water freshly boiled to expel carbon dioxide. This makes 200 cc. of sugar solution. The lime is mixed dry with the sugar and the water added later to keep the lime from lumping. After shaking the sugar solution one hour titrate 50 cc. of it with N/2 hydrochloric acid in presence of methyl orange indicator. The acid used is equivalent to the carbonate and hydroxide in 0.25 gram of the sample.

Filter the remainder of the sugar solution, discarding the first 25 cc. of filtrate. Titrate 50 cc. of the filtrate with N/2 hydrochloric acid in presence of methyl orange indicator. The acid used is equivalent to the hydroxide in 0.25 gram of the sample.

If a 1 gram sample is used the percentage of calcium oxide (CaO) is equal to 5.6 times the number of cubic centimeters of hydrochloric acid used in the second titration; and the percentage of calcium carbonate (CaCO_{3}) equivalent to the carbonate present is equal to 10 times the difference in cubic centimeters between the results of the two titrations.

SULFATE OF IRON.

INSOLUBLE MATTER.

Treat 10 grams of the sample with 100 cc. of freshly boiled distilled water cooled to 30° C. or less. When solution is complete filter through a weighed Gooch crucible, wash, dry, cool, and weigh. Report the weight of the residue, in percentage, as insoluble matter.

IRON AS FERROUS SULFATE.

Dissolve 1 gram of the sample and dilute to 200 cc. with freshly boiled distilled water cooled to 30° C. or less. Add 5 cc. of dilute sulfuric acid (1 to 3) to a 50 cc. portion of the solution and titrate with N/10 potassium permanganate. The percentage of ferrous sulfate (FeSO{4}.7H{2}O) is equal to 11.12 times the number of cubic centimeters of potassium permanganate used.

ACIDITY.

Shake 12.25 grams of the sample in a 150 cc. bottle with 75 cc. of 95 per cent alcohol for ten minutes. Run a blank. Filter rapidly both sample and blank and wash rapidly with alcohol sufficient to make 100 cc. of filtrate. Titrate with N/20 sodium hydroxide in presence of phenolphthalein and subtract the result of titrating the blank from that of titrating the solution of the sample. The percentage of acidity, expressed as sulfuric acid (H{2}SO{4}), is equal to 0.02 times the number of cubic centimeters of sodium hydroxide used.

SODA ASH.

INSOLUBLE MATTER.

Treat 5.305 grams of the sample with 200 cc. of freshly boiled and cooled distilled water. When solution is complete filter through an asbestos mat in a weighed Gooch crucible, dry, cool, and weigh. Report the weight of the residue, in percentage, as insoluble matter.

AVAILABLE ALKALI.

Dilute the filtrate from the determination of insoluble matter to 1,000 cc. and thoroughly mix. Titrate 25 cc. of this dilution with N/10 hydrochloric acid in presence of methyl orange indicator. The percentage of available alkali, expressed as sodium carbonate (Na{2}CO{3}), is equal to 4 times the number of cubic centimeters of hydrochloric acid used.

CHEMICAL BIBLIOGRAPHY.

The subjoined bibliography comprises the publications cited in the text of this report. The references are arranged alphabetically by authors’ names and under each author in order of dates of publication. When different pages of a single work are cited letters are used in connection with the number that refers to the work.

Bibliography 1:

ANDREWS, L. W. Sprengel’s method for colorimetric determination of nitrates: J. Am. Chem. Soc., Vol. 26, pp. 388–91, 1904.

Bibliography 1a:

a. ASSOC. OFF. AG. CHEMISTS. Determination of iodine and bromine: J. A. O. A. C., Vol. 1, No. 4, pt. 1, pp. 47–8, 1916.

Bibliography 1b:

b. BACHMANN, FRANK. A new seal for the prevention of aeration in deaerated liquids: J. Ind. Eng. Chem., Vol. 6, pp. 764–5, 1914.

Bibliography 2: