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Nitric Acid → Nitric Acid

HRID 377127
ノート
印刷プレビュー

反応式

HRID 377127 の反応式
[N+:1]([O-:4])([OH:3])=[O:2].C1(N)C=CC([NH2:11])=CC=1>>[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+:11]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 944Nitric Acid3 回HCID 7814P-Phenylenediamine

生成物 3

HCID 944Nitric AcidHCID 22985Ammonium nitrateHCID 26045Hydroxylamine, nitrate

実験手順

The general procedure of Example 1 is repeated except that a piece of graphite felt is attached to the graphite cathode to enhance the cathode surface area. A solution containing 0.5 M nitric acid and 50 mM 1,4-phenylenediamine is charged to the catholyte 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 5.5 volts is applied. The catholyte is stirred under application of the current. A solution of 1.67 M hydroxylammonium nitrate and 0.50 M nitric acid with no detectable ammonium nitrate is obtained from the catholyte compartment. An overall current efficiency of 85% for formation of hydroxylammonium nitrate is achieved.

後処理

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

出典と根拠

ORDレコード
ord-208046fef48542eb9c0e0ee068a40d99
出典データセット
uspto-grants-2000_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06024855

反応ノート

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