Reacción #75331

ord-c54d522ea3d64a909f8f52bdf6327b68

Ecuación de reacción

CO
methanol
O=C(O)[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO
gluconic acid
ClOCl.[Hf]
hafnium oxychloride
→
O=C(O)[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO
gluconic acid
[Hf]
hafnium

Reactantes

CO
methanol
O=C(O)[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO
gluconic acid
ClOCl.[Hf]
hafnium oxychloride

Reactivos

Ninguno

Disolventes

—
aqueous solution

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroto precipitate the hafnium-gluconate
  2. 2
    Temperaturathe suspension was heated to 60°
  3. 3
    workup.ADDITIONThe pH of the preparation was then adjusted to 6.5 by addition of concentrated NH4OH
  4. 4
    FiltraciónThe hot solution was filtered
  5. 5
    Otroto remove NH4Cl and ammonium gluconate
  6. 6
    OtroThe precipitate was dried at 90° for 1 hour
  7. 7
    Otroresuspended in anhydrous methanol at 60°
  8. 8
    workup.STIRRINGwith stirring for 60 minutes
  9. 9
    Filtraciónthen filtered
  10. 10
    Otroto remove additional excess of NH4Cl and ammonium-gluconate
  11. 11
    ExtracciónThe precipitate was further extracted
  12. 12
    Otroto remove additional NH4Cl and ammonium-gluconate employing anhydrous methanol
  13. 13
    Extracciónin a Soxhlet apparatus, extraction
  14. 14
    OtroThe precipitate was then dried at 90° for approximately 2 hours

Procedimiento

Hydrated hafnium-ammonium-gluconate was prepared as follows: 125 grams of hafnium oxychloride.8H2O was dissolved in 600 ml of 50% aqueous solution gluconic acid. Four litters of anhydrous methanol were added to precipitate the hafnium-gluconate and the suspension was heated to 60° with stirring for 30 minutes. The pH of the preparation was then adjusted to 6.5 by addition of concentrated NH4OH. The hot solution was filtered to remove NH4Cl and ammonium gluconate. The precipitate was dried at 90° for 1 hour, resuspended in anhydrous methanol at 60° with stirring for 60 minutes then filtered to remove additional excess of NH4Cl and ammonium-gluconate. The precipitate was further extracted to remove additional NH4Cl and ammonium-gluconate employing anhydrous methanol in a Soxhlet apparatus, extraction was continued until the methanol surrounding the precipitate was clear. The precipitate was then dried at 90° for approximately 2 hours and ground to a fine powder. Elemental analysis was consistent with a formula of (HfO)2 (NH 4)2 gluconate3 (H2O)x. It was found that the same final product was obtained when the molar ratio of gluconic acid to hafnium was varied from 1:1 to 100:1. Moreover, the same product was obtained utilizing hafnium-tetrachloride instead of hafnium-oxychloride.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04176173uspto-grants-1979_11