Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Maleic Anhydride | HCID 7923 | — |
| Edukt | Ammonium Hydroxide | HCID 14923 | — |
| Edukt | 2-Hydroxy-1,2,3-propanetricarboxylic acid hydrate (1:1) | HCID 22230 | — |
| Edukt | Hexanediamine | HCID 134940 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | Citric Acid | HCID 311 | — |
| Produkt | Hexanediamine | HCID 134940 | — |
Reaktionsschritte
A solution of 2.1 g (0.01 moles) of citric acid monohydrate (Formula weight 210) and 0.32 g (0.0028 moles) hexanediamine was added to 19.6 g (0.2 mole) maleic anhydride which had been dissolved in 40 ml water at 80°-90° C., and finally 30 g of 30% aqueous solution of ammonium hydroxide (0.22 mol NH3) was added. This solution was evaporated to dryness over a period of 30 minutes. The solid was then heated at 195°-220° C. for 10 minutes, removed from the heat, allowed to cool and broken up with a spatula. The solid was then heated at 230°-245° C. for 10 minutes, removed from the heat, allowed to cool and broken up with a spatula. Finally, the solid was heated at 230°-245° C. for 10-15 minutes, removed from the heat and allowed to cool to room temperature. The resulting water insoluble polymer was slurried in 40.0 ml of water and a solution of 8.0 g of sodium hydroxide in 12 ml of water was added over 5 minutes. The solution was stirred for 10-20 minutes to give a clear red-brown solution, pH 10-11.0 of a copolymer of polyaspartic acid, citric acid and hexanediamine. The tests for CaSO4, Example 3, and CaCO3 (below) were run and the result are recorded in Table 2.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05488088 |
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| Quelldatensatz | uspto-grants-1996_01 |
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| ORD ID | ord-7bf05d39afc146caa26d61eb27722980 |
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| Quellennotiz | uspto-grants-1996_01 |
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