Phosphoric Acid → Zirconium phosphate

HRID 400319

Reaktionsgleichung

Reaktionsgleichung von HRID 400319
[OH-].[Zr+4:2].[OH-].[OH-].[OH-].[Zr].[P:7](=[O:11])([OH:10])([OH:9])[OH:8].[P]>O>[P:7]([O-:11])([O-:10])([O-:9])=[O:8].[Zr+4:2].[P:7]([O-:11])([O-:10])([O-:9])=[O:8].[P:7]([O-:11])([O-:10])([O-:9])=[O:8].[P:7]([O-:11])([O-:10])([O-:9])=[O:8].[Zr+4:2].[Zr+4:2]

Komponenten

6

Reaktionsbedingungen

Temperatur
80 °C

Versuchsvorschrift

Catalyst preparation. A zirconium phosphate based catalyst was prepared by a co-precipitation method. A solution of zirconium hydroxide (Zr(OH)4) as a zirconium precursor was dissolved in deionized water. To this solution, a stoichiometric amount of phosphoric acid as a phosphorus precursor was added. The resulting mixture was heated at 80° C. for 2 hours to remove water, and a paste was obtained. The resulting paste was then dried in an oven at 100° C. overnight (about 12-18 hours) to remove the bulk of any remaining water, and to provide a powder. The powder was then calcined at 350° C. for 2 hours to obtain powdered zirconium phosphate.

Aufarbeitung

  1. customCatalyst preparation
  2. customA zirconium phosphate based catalyst was prepared by a co-precipitation method
  3. customto remove water
  4. customa paste was obtained
  5. customThe resulting paste was then dried in an oven at 100° C. overnight (about 12-18 hours)
  6. customto remove the bulk of any remaining water
  7. customto provide a powder

Quellen und Nachweise

ORD-Eintrag
ord-5158bc0245e144c6ba10bfddbe185877
Quelldatensatz
uspto-grants-2014_06
Patentnummer
US08741258B2

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