Nickel → Nickel

HRID 1611565

反応式

HRID 1611565 の反応式
[Ni:1].[Zn:2].[O-:3][P:4]([O:7][P:8]([O-:11])([O-:10])=[O:9])(=[O:6])[O-:5].[Zn+2].[Zn+2].S([O-])([O-])(=O)=O.[Ni+2].[O-]P(OP([O-])([O-])=O)(=O)[O-].[K+].[K+].[K+].[K+]>[Zn].[Ni].[Cu]>[O-:5][P:4]([O:7][P:8]([O-:11])([O-:10])=[O:9])(=[O:3])[O-:6].[Ni:1].[Zn:2]

参加物

10

反応物 5

HCID 935Nickel3 回HCID 23740Potassium pyrophosphate2 回HCID 23994Zinc3 回HCID 24586Nickel SulfateHCID 62641Zinc pyrophosphate

生成物 3

HCID 935NickelHCID 23994ZincHCID 644102Pyrophosphate

試薬・触媒・溶媒 2

HCID 23978Copper触媒HCID 14877100Nickel--zinc (1/1)溶媒2 回

実験手順

However, the composition of nickel and zinc in the nickel-zinc alloy layer 5 was purposely deviated from the range according to the present invention in which the content of nickel is 70 to 88 wt % and the content of zinc is the balance. Thus, for this nickel-zinc alloy layer 5, a pyrophosphate based solution was prepared using zinc pyrophosphate (ZnP2O7·3H2O), nickel sulfate (NiSO4·7H2O) and potassium pyrophosphate (K2P4O7) so that the solution had a composition with 1.0 g/l of zinc, 1.5 g/l of nickel and 100 g/l of potassium pyrophosphate, and in the solution at a liquid temperature of 30° C., the copper foil itself was made to undergo cathode polaraization with the use of a stainless plate for the counter electrode under conditions of current density of 1 A/dm2 and electrolysis time of 300 seconds, thereby providing an alloy composition with 1.14 g/m2 (59.1 wt %) of nickel and 0.79 g/cm2 (40.9 wt %) of zinc. The weight thickness of the nickel-zinc alloy layer 5 was 1.93 g/m2. In concurrence with this formation of the nickel-zinc alloy layer 5 on the nodular treatment side 4, 0.10 g/m2 of nickel-zinc layer was formed on the shiny side 6 of the untreated copper foil 2 as a corrosion prevention layer.

後処理

  1. customat a liquid temperature of 30° C.
  2. customelectrolysis time of 300 seconds

出典と根拠

ORDレコード
ord-b6b1fdadb9b047bb8cc73465742715bc
出典データセット
uspto-grants-2006_01
特許番号
US06989199B2

関連ノート

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