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  2. Boric acid - Wikipedia

    en.wikipedia.org/wiki/Boric_acid

    Boric acid is a weak acid, with pK a (the pH at which buffering is strongest because the free acid and borate ion are in equal concentrations) of 9.24 in pure water at 25 °C. But apparent p K a is substantially lower in swimming pool or ocean waters because of interactions with various other molecules in solution.

  3. Boron trioxide - Wikipedia

    en.wikipedia.org/wiki/Boron_trioxide

    Another method is heating boric acid above ~300 °C. Boric acid will initially decompose into steam, (H 2 O (g)) and metaboric acid (HBO 2) at around 170 °C, and further heating above 300 °C will produce more steam and diboron trioxide. The reactions are: H 3 BO 3 → HBO 2 + H 2 O 2 HBO 2 → B 2 O 3 + H 2 O. Boric acid goes to anhydrous ...

  4. Boric acid (data page) - Wikipedia

    en.wikipedia.org/wiki/Boric_acid_(data_page)

    This page provides supplementary chemical data on boric acid. Thermodynamic properties. Phase behavior ... Heat capacity, c p? J/(mol K) Liquid properties

  5. Borax - Wikipedia

    en.wikipedia.org/wiki/Borax

    Borax is also easily converted to boric acid and other borates, which have many applications. Its reaction with hydrochloric acid to form boric acid is: Na 2 B 4 O 7 ·10H 2 O + 2 HCl → 4 H 3 BO 3 + 2 NaCl + 5 H 2 O. Borax is sufficiently stable to find use as a primary standard for acid-base titrimetry. [17]: p.316

  6. Boron trifluoride - Wikipedia

    en.wikipedia.org/wiki/Boron_trifluoride

    Boron trifluoride reacts with water to give boric acid and fluoroboric acid. The reaction commences with the formation of the aquo adduct, H 2 O−BF 3, which then loses HF that gives fluoroboric acid with boron trifluoride. [22] 4 BF 3 + 3 H 2 O → 3 H[BF 4] + B(OH) 3. The heavier trihalides do not undergo analogous reactions, possibly due to ...

  7. Borate esters - Wikipedia

    en.wikipedia.org/wiki/Borate_esters

    In organic chemistry, borate esters are organoboron compounds which are conveniently prepared by the stoichiometric condensation reaction of boric acid with alcohols. There are two main classes of borate esters: orthoborates, B(OR) 3 and metaborates, B 3 O 3 (OR) 3. Metaborates contain 6-membered boroxine rings.

  8. Thermometric titration - Wikipedia

    en.wikipedia.org/wiki/Thermometric_titration

    Acidic solutions of fluoride (including hydrofluoric acid) can be determined by a simple thermometric titration with boric acid. B(OH) 3 + 3F − + 3H + ↔ BF 3 + 3H 2 O The titration plot illustrated in Figure 19 shows that the endpoint is quite rounded, suggesting that the reaction might not proceed to stoichiometric equilibrium.

  9. Tetrafluoroborate - Wikipedia

    en.wikipedia.org/wiki/Tetrafluoroborate

    Potassium fluoroborate is obtained by treating potassium carbonate with boric acid and hydrofluoric acid. B(OH) 3 + 4 HF → HBF 4 + 3 H 2 O 2 HBF 4 + K 2 CO 3 → 2 KBF 4 + H 2 CO 3. Fluoroborates of alkali metals and ammonium ions crystallize as water-soluble hydrates with the exception of potassium, rubidium, and cesium.