Diammonium succinate → Succinic Acid
Reaction equation
[C:1]([O-:8])(=[O:7])[CH2:2][CH2:3][C:4]([O-:6])=[O:5].[NH4+:9].[NH4+].S([O-])([O-])(=O)=O.[NH4+].[NH4+]>O>[C:1]([O-:8])(=[O:7])[CH2:2][CH2:3][C:4]([O-:6])=[O:5].[NH4+:9].[NH4+:9].[C:1]([OH:8])(=[O:7])[CH2:2][CH2:3][C:4]([OH:6])=[O:5]Participants
5
Reactant 2
Product 2
Reagents, catalysts & solvents 1
Procedure
Operations involving Streams 3, 4, 5, 11, 12, 13 and 15 in FIGS. 1 and 2 were simulated based on the data collected in Experiments I, II and III. From Experiment I, a pH value of 1.6 was chosen as the target pH for the crystallization of succinic acid. From Experiment II, 80% w/w methanol solution was chosen as the target methanol-water ratio for the crystallization of sulfates. Using the results of Experiment III, the initial concentration of ammonium succinate was chosen such that there would have been sufficient water to solubalize ammonium sulfate produced in the conversion of ammonium succinate into succinic acid. This precaution was taken to minimize contamination of succinic acid by sulfates.
Workup
- customcollected in Experiments I, II and III
- customFrom Experiment I, a pH value of 1.6 was chosen as the target pH for the crystallization of succinic acid
- customFrom Experiment II, 80% w/w methanol solution was chosen as the target methanol-water ratio for the crystallization of sulfates
- customresults of Experiment III
Sources & evidence
- ORD record
- ord-5ac7416bb3fc41a8ab1f820344dcf2ab
- Source dataset
- uspto-grants-1999_09
- Patent number
- US05958744
Reaction notes
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