Boric Acid → Boric acid (HBO2), zinc salt (2:1)

HRID 1837195

Reaction equation

HRID 1837195 reaction equation
[B:1]([OH:4])([OH:3])[OH:2].[Zn:5]>O>[B:1]([O-:4])([O-:3])[O-:2].[Zn+2:5].[B:1]([O-:4])([O-:3])[O-:2].[Zn+2:5].[Zn+2:5]

Participants

4

Procedure

An aqueous solution was prepared by dissolving 72.5 g of boric acid (B2O3 content of 56.3%) in 1000 ml of pure water. To the aqueous solution were added 95.7 g of a zinc flower (ZnO content of 99.4%) and 217.5 g of boric acid (B2O3 content of 56.3%), and were stirred and mixed together such that the molar ratio of B2O3/ZnO was 2.0. Next, the solution was stirred and reacted at 35° C. for 120 minutes. The solution was further stirred and reacted at 90° C. for 4 hours. The obtained product was filtered, washed with water and was, then, dried at 105° C. to obtain a zinc borate (sample H-1). Table 3 shows the chemical composition and properties of the thus obtained zinc borate (sample H-1), FIG. 18 shows an X-ray diffraction image thereof, and FIG. 19 shows an electron microphotograph thereof. From FIG. 18, the obtained zinc borate (sample H-1) was the one of the 2.3 type, but was in the form of mixed crystals of a heptahydrate (2ZnO.3B2O3.7H2O) and a 3.5 type zinc borate (3ZnO.5B2O3.14H2O), exhibiting a peak due to unreacted zinc oxide. The 2.3 type zinc borate was not obtained in a pure form.

Workup

  1. customAn aqueous solution was prepared
  2. additionmixed together such that the molar ratio of B2O3/ZnO
  3. stirringNext, the solution was stirred
  4. customreacted at 35° C. for 120 minutes
  5. stirringThe solution was further stirred
  6. customreacted at 90° C. for 4 hours
  7. filtrationThe obtained product was filtered
  8. washwashed with water
  9. customdried at 105° C.

Sources & evidence

ORD record
ord-b7ec7731f33b4eebb81b9bf38547bb26
Source dataset
uspto-grants-2004_08
Patent number
US06780913B2

Linked notes

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