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llms.txt · MCP-AnleitungDatenschutz · Nutzungsbedingungen · Supportv1.8.0
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Hydroquinone → Nitric Acid

HRID 377129
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 377129
[N+:1]([O-:4])([OH:3])=[O:2].C1(C=CC(O)=CC=1)O>>[N+:1]([O-:4])([O-:3])=[O:2].[OH:2][NH3+:1].[N+:1]([O-:4])([OH:3])=[O:2].[N+:1]([O-:4])([O-:3])=[O:2].[NH4+:1]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 2

HCID 785HydroquinoneHCID 944Nitric Acid4×

Produkt 3

HCID 944Nitric AcidHCID 22985Ammonium nitrateHCID 26045Hydroxylamine, nitrate

Versuchsvorschrift

The general procedure of Example 8 is repeated except that a solution of 1 M nitric acid and 100 ppm hydroquinone is charged to the catholyte compartment. A solution of 4 M nitric acid is charged to the anolyte compartment. Concentrated nitric acid is added to the catholyte compartment to maintain the nitric acid concentration between 0.5 M and 1 M under application of an electrical current. While maintaining the temperature between 5° C. and 10° C., a current of 20 amps (5 ASI) and a cell voltage of about 6.5 volts is applied. A solution of 1.3 M hydroxylammonium nitrate and 0.8 M nitric acid with no detectable ammonium nitrate is obtained from the catholyte compartment. An overall current efficiency of 60% for formation of hydroxylammonium nitrate is achieved.

Aufarbeitung

  1. additionis charged to the catholyte compartment
  2. temperatureWhile maintaining the temperature between 5° C. and 10° C.

Quellen und Nachweise

ORD-Eintrag
ord-6a08f2aff9c044dba040dd6bbd130ad6
Quelldatensatz
uspto-grants-2000_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06024855

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