Nitric Acid → Calcium nitrate
Reaction equation
[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[F-].[Ca+2:17].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[N+:22]([O-:25])([OH:24])=[O:23].O=P12OP3(OP(OP(O3)(O1)=O)(=O)O2)=O>>[N+:22]([O-:25])([O-:24])=[O:23].[Ca+2:17].[N+:22]([O-:25])([O-:24])=[O:23]Participants
Conditions
- Temperature
- 20 °C
Procedure
303.9 g of phosphonitrate solution obtained by attacking 100 g of Morocco phosphate rock with 228 g of 58% nitric acid, having a content of CaO of 16.62% and of P2O5 of 11.83%, were introduced into a crystallizing vessel. The solution was cooled at a rate of cooling of 12° C/hour, and when the temperature of the solution reached 20° C, a temperature rise from 20° to 24° C was recorded. The solution was then further cooled at the same rate of 12° C/hour until it again reached 20° C. At this instant, into the solution were introduced under stirring 95 g of mother solution with washing acid, coming from the second step of another sample subjected to crystallization, which had a content of P2O5 of 14.94%, and CaO 4.28%, cooling being continued at a rate of 30° C/hour until reaching the temperature of -5° C. The crystal suspension was filtered and centrifuged, obtaining thus 210 g of calcium nitrate crystals having a content of CaO of 20% and of P2O5 of 0.51%, a largest size of 350 microns, minimum size of 110 microns and an average size of 200 microns. In this case the liquid: solid ratio had been of about 1:1.1. By centrifuging, an amount of 110 g of mother solution was also obtained, having a content of CaO of 2.61% and of P2O5 17.45%, the rest of the solution being included in the filtered crystals.
Workup
- temperatureThe solution was cooled at a rate
- temperatureof cooling of 12° C/hour, and when the temperature of the solution
- customreached 20° C
- customfrom 20° to 24° C
- additionAt this instant, into the solution were introduced
- washwith washing acid
- customsubjected to crystallization, which
- temperature28%, cooling
- customthe temperature of -5° C
- filtrationThe crystal suspension was filtered
Sources & evidence
- ORD record
- ord-06d07b69ccd949309e294067226d4ed9
- Source dataset
- uspto-grants-1977_02
- Patent number
- US04008309
Reaction notes
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