Boric acid

Definition and stakes

1911 Encyclopædia Britannica (1911)

“ BORIC ACID, or Boracic Acid, H3BO3, an acid obtained by dissolving boron trioxide in water. It was first prepared by Wilhelm Homberg (1652–1715) from borax, by the action of mineral acids, and was given the name sal sedativum Hombergi. The presence of boric acid or its salts has been noted in sea-water, whilst it is also said to exist in plants and especially in almost all fruits (A. H. Allen, Analyst, 1904, 301) . The free acid is found native in certain volcanic districts such as Tuscany, the Lipari Islands and Nevada, issuing mixed with steam from fissures in the ground ”
Source: Wikisource

C. Beringer,  A Text-book of Assaying: For the Use of Those Connected with Mines

“ Boric acid is also a [Pg 430] constituent of certain silicates, such as tourmaline, axinite, and datholite.
The natural borates are used in the preparation of borax, which is largely employed as a preservative agent, for fluxing, and for other purposes.
There is only one series of boron compounds which have any importance. These are the borates in which the trioxide (B2O3) acts the part of a weak acid. The addition of any acid liberates boric acid, which separates out in cold solutions as a crystalline precipitate.
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Source: Gutenberg

1911 Encyclopædia Britannica (1911)

“ After fusion the mass solidifies to a transparent vitreous solid which dissolves readily in water to form boric acid (q.v.) ; it is exceedingly hygroscopic and even on standing in moist air becomes opaque through absorption of water and formation of boric acid. Its specific gravity is 1.83 (J. Dumas) . It is not volatile below a white heat, and consequently, if heated with salts of more volatile acids, it expels the acid forming oxide from such salts; for example, if potassium sulphate be heated with boron trioxide, sulphur trioxide is liberated and potassium borate formed. ”
Source: Wikisource

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