Reaktionsgleichung
O.[OH:2][C@H:3]1[O:22][C@H:21]([CH2:23][OH:24])[C@@H:8]([O:9][C@@H:10]2[O:18][C@H:17]([CH2:19][OH:20])[C@H:15]([OH:16])[C@H:13]([OH:14])[C@H:11]2[OH:12])[C@H:6]([OH:7])[C@H:4]1[OH:5].O.C(=O)=O>CO>[OH:2][CH:3]1[O:22][C@H:21]([CH2:23][OH:24])[C@@H:8]([O:9][C@@H:10]2[O:18][C@H:17]([CH2:19][OH:20])[C@H:15]([OH:16])[C@H:13]([OH:14])[C@H:11]2[OH:12])[C@H:6]([OH:7])[C@H:4]1[OH:5]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
0.3 g of alpha-lactose monohydrate was dissolved in 2 ml deionized water, 98 ml of methanol was added to the aqueous solution and the mixture was introduced into the 32 ml particle formation vessel through the three-passage nozzle. The operating conditions were 270 bar and 70° C. inside the vessel, a solution flow rate (in the intermediate nozzle passage) of 0.5 ml/min and a supercritical CO2 flow rate (in the inner and outer passages) of 7.5 ml/min. The product (a fine white powder) was collected at the end of the experiment. An SEM micrograph and XRD pattern for the product are shown in FIGS. 5 and 6 respectively.
Aufarbeitung
- additionwas added to the aqueous solution
- additionthe mixture was introduced into the 32 ml particle formation vessel through the three-passage nozzle
- custom270 bar and 70° C.
- customThe product (a fine white powder) was collected at the end of the experiment
Quellen und Nachweise
- ORD-Eintrag
- ord-80bc64e753634d1589d0596b32a2d336
- Quelldatensatz
- uspto-grants-2000_05
- Patentnummer
- US06063138
Verknüpfte Notizen
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