The standard normal solution of hydrochloric acid is made by diluting 100 c.c. of the strong acid to one litre with water. This will be approximately normal. In order to determine its exact strength, weigh up 3 grams of recently ignited pure sodium carbonate or of the ignited bicarbonate. Transfer to a flask and dissolve in 200 c.c. of water; when dissolved, cool, tint faintly yellow with a few drops of a solution of methyl orange, and run in the standard "acid " from a burette till the yellow changes to a pink. Read off the number of c.c. used, and calculate to how much sodium carbonate 100 c.c. of the "acid" are equivalent. If the "acid" is strictly normal, this will be 5.3 grams. It will probably be equivalent to more than this. Now calculate how much strictly normal "acid" would be equivalent to the standard found. For example: suppose the standard found is 5.5 gram of sodium carbonate, then—

5.3 : 5.5 :: 100 : x
(where x is the quantity of normal "acid" required).
x = 103.8 c.c.

To get the "acid" of normal strength, we should then add 3.8 c.c. of water to each 100 c.c. of the standard solution remaining. Suppose there were left 930 c.c. of the approximate "acid," 35.3 c.c. of water must be added and mixed. It should then be checked by another titration with pure sodium carbonate.

The standard solution of semi-normal "alkali." The best alkali for general purposes is ammonia, but, since it is volatile (especially in strong solutions), it is best to make it of half the usual strength, or semi-normal. One litre of this will contain 8.5 grams of ammonia (NH3), and 100 c.c. of it will just neutralise 50 c.c. of the normal "acid." Take 100 c.c. of dilute ammonia and dilute with water to one litre. Run into a flask 50 c.c. of the standard "acid," tint with methyl orange, and run in from a burette the solution of ammonia till neutralised. Less than 100 c.c. will probably be used. Suppose 95 c.c. were required, there should have been 100, hence there is a deficiency of five. Then, for each 95 c.c. of standard "ammonia" left, add 5 c.c. of water, and mix well. 100 c.c. will now be equivalent to 50 c.c. of the "acid."

As an example of the application of this method, we may take the determination of lime in limestone, marble, and similar substances.

Determination of Lime in Limestone.—Weigh up 1 gram of the dried sample, and dissolve in 25 c.c. of normal acid, cool, dilute to 100 c.c., and titrate with the semi-normal solution of alkali (using methyl-orange as an indicator). Divide the c.c. of alkali used by 2, subtract from 25, and multiply by 0.028 to find the weight of lime. This method is not applicable in the presence of other carbonates or oxides, unless the weight of these substances be afterwards determined and due correction be made.

STRONTIA.

Strontia, the oxide of strontium (SrO), occurs in nature as sulphate, in the mineral celestine (SrSO4), and as carbonate in strontianite (SrCO3). It is found in small quantities in limestones, chalk, &c.

Strontia is used in sugar-refining, and for the preparation of coloured lights.

Detection.—It is detected by the crimson colour which its compounds (when moistened with hydrochloric acid) impart to the flame. The spectrum shows a large number of lines, of which a red, an orange, and a blue are most characteristic.