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Copper(II) nitrate trihydrate → Cupric nitrate

HRID 1154520
ノート
印刷プレビュー

反応式

HRID 1154520 の反応式
O.O.O.[N+:4]([O-:7])([O-:6])=[O:5].[Cu+2:8].[N+:9]([O-:12])([O-:11])=[O:10]>O>[N+:4]([O-:7])([O-:6])=[O:5].[Cu+2:8].[N+:9]([O-:12])([O-:11])=[O:10]
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 1

HCID 9837674Copper(II) nitrate trihydrate

生成物 1

HCID 18616Cupric nitrate

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

Five Hundred and seventy grams of Cu(NO3)2.2.5H2O (typically designated as copper (II) nitrate trihydrate) was dissolved in water and diluted to 2.0 liters to give 1.25 molar copper nitrate solution. An 18% sodium hydroxide solution was prepared by dissolving 2.5 grams sodium hydroxide in water and diluting to 1.0 liter. The caustic solution was allowed to cool to room temperature before using in the reaction that follows. Sodium bicarbonate, 8.4 grams, 0.1 mole, was added to a three liter reactor and was dissolved in 0.25 liter of water to allow for agitation. The pH of the bicarbonate solution was raised to 11.5 with sodium hydroxide. (This prevents carbon dioxide formation on addition of the relatively acidic cupric nitrate solution due to lowering the pH below about 6). The aqueous carbonate medium is agitated and an aliquot of the copper nitrate solution (80.1 ml, 0.1 moles) is added. The resulting intermediate which forms immediately is then converted to the hydroxide by the addition of approximately 37 ml of the above caustic solution. After sixteen cupric nitrate-sodium hydroxide cycles the temperature of the slurry had reached 32° C. with a pH of 10.1 The solution was then filtered under vacuum conditions and washed with water. The copper assay was 56.59% after drying for five hours at 65° C. The copper was recovered quantitatively.

後処理

  1. additiondiluted to 2.0 liters

出典と根拠

ORDレコード
ord-7c86b7dbe0cf4b15ae259cd03743f7cf
出典データセット
uspto-grants-1984_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04490337

反応ノート

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