Ammonium Hydroxide → Antimony oxalate

HRID 1987531

Reaktionsgleichung

Reaktionsgleichung von HRID 1987531
[C:1]([O-:4])(=[O:3])[CH3:2].[Sb+3:5].[C:6]([O-:9])(=[O:8])[CH3:7].[C:10]([O-:13])(=[O:12])[CH3:11].[OH-:14].[NH4+].[Sb]>O.C(O)(=O)C(O)=O>[C:1]([O-:4])(=[O:3])[C:2]([O-:8])=[O:14].[Sb+3:5].[C:6]([O-:9])(=[O:8])[C:7]([O-:12])=[O:14].[C:10]([O-:13])(=[O:12])[C:11]([O-:3])=[O:14].[Sb+3:5]

Komponenten

6

Reaktionsbedingungen

Temperatur
60 °C

Versuchsvorschrift

Antimony oxalate solution was prepared by mixing antimony (III) acetate as obtained from Aldrich with a 1 M solution of oxalic acid in deionized water and heating the mixture to 60° C. A concentrated solution of ammonium hydroxide in deionized water was added dropwise to the antimony containing mixture until the solution became homogeneous. At this point, the solution was diluted as-required with oxalic acid solution or deionized water to desired metal concentration. The prepared antimony oxalate solution (3.3% antimony, 290.9 μL) was mixed with deionized water (1149.1 μL) and the resultant diluted solution (120 μL) was added to the supported rhodium-indium product of the first impregnation step and agitated by vibration for 30 minutes at room temperature. The obtained trimetallic material was dried at 120° C. for 2 hours and then calcined in air at 450° C. for 4 hours.

Aufarbeitung

  1. concentrationto desired metal concentration
  2. additionThe prepared antimony oxalate solution (3.3% antimony, 290.9 μL) was mixed with deionized water (1149.1 μL)
  3. additionthe resultant diluted solution (120 μL) was added to the supported rhodium-indium product of the first impregnation step
  4. customThe obtained trimetallic material was dried at 120° C. for 2 hours
  5. waitcalcined in air at 450° C. for 4 hours

Quellen und Nachweise

ORD-Eintrag
ord-60750c09de864974ba4571e2fc4f3a33
Quelldatensatz
uspto-grants-2009_06
Patentnummer
US07550637B2

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