Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphoric Acid | HCID 1004 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Zirconium(IV) sulfate | HCID 26793 | — |
| Reactant | Phosphorus | HCID 5462309 | — |
| Solvent | Water | HCID 962 | — |
| Product | Zirconium phosphate | HCID 160986 | — |
Reaction Steps
Amorphous zirconium phosphate was prepared in all the examples. In this example the material was prepared according to the following procedure. In the first stage, a slurry containing 440 g of basic zirconium sulfate (40% ZrO2) (MEI, HCP PP142A), with a predetermined particle size distribution ranging from 50 to 60 microns, in a phosphorus-containing solution was made. The phosphorus-containing solution had the following composition: 3.3 kg of water, 402 g of 75 wt % H3PO4, 380 g of 30 wt % NaOH and 45 g of Na4SiO4. The slurry was transferred into an autoclave, sealed and heated at 160° C. for 3 hours under constant stirring. The resulting product of conversion was filtered, washed with 0.5 kg of water and re-slurried in 2 L of 1 M H2SO4. The zirconium phosphate slurry in sulfuric acid was heated to the boiling point and kept at this temperature for 1 hour. After cooling down, the zirconium phosphate was filtered, washed with 0.5 kg of water and re-slurried in 1 L of water. To the ZrP suspension a 30 wt % NaOH solution was added gradually for 30 to 40 minutes to raise the pH to 7.0. Then, the zirconium phosphate was filtered, washed with 1 kg of water and dried at 150° C. for 12 hours in air.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06936175B2 |
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| Source dataset | uspto-grants-2005_08 |
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| ORD ID | ord-af0dffba1f8943f9a75bf4c5009644c5 |
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| Source note | uspto-grants-2005_08 |
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