Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Zinc | HCID 23994 | — |
| Reactant | Zinc nitrate hexahydrate | HCID 15865313 | — |
| Reactant | Zn phosphate | HCID 131721340 | — |
| Reactant | HCID 178435160 | HCID 178435160 | — |
| Product | Zinc Phosphate | HCID 24519 | — |
Reaction Steps
An aqueous solution of 8.51 g 50 wt % H3PO2 in 8.00 g distilled water was prepared as described in Example 1. To this solution was added 28.78 g zinc nitrate hexahydrate salt, Zn(NO3)2.6H2O (ACS reagent, Aldrich Chemical Co., Inc. #22,873-7, CAS # 10196-18-6), equivalent to 21.97 wt % Zn. The molar ratio of Zn/phosphate in this mixture was 3/2 and the equivalent solids level [as Zn3(PO4)2] was 27.5 wt %. Endothermic dissolution of the zinc nitrate hexahydrate proceeded giving a homogeneous solution once the sample warmed to room temperature. Further warming of this solution to >25° C. on a hotplate initiated a reaction in which the solution vigorously evolved red-brown acrid fumes of NOx(g). The reaction continued for approximately 10 minutes while the sample remained a clear, colorless solution, abated somewhat for a period of five minutes, then vigorously resumed finally resulting in the formation of a mass of moist white solid, some of which was very adherent to the walls of the Pyrex beaker used as a reaction vessel. The hot solid was allowed to cool to room temperature and was stored in a polyethylene vial.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08734822B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-c5a58f28663b4de48b5320c103fe2728 |
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| Source note | uspto-grants-2014_05 |
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