摘要
The micro-amount of nickel in MnO2, electrolytical and natural both, was determined by differential pulse polarography. NH4OH-NH4Cl was used as supporting electrolyte. It was found that the peak potential of Ni(II) reduction wave is -1.0V (vs. Ag-AgCl electrode). The presence of great amount of Mn(II) does not interfere in the trace nickel determination. the peak current relationship with the Ni2+ concentration presents a quite fine straight line. The differential pulse polarography is proved that it is a simple, reliable and acceptable method for determination of trace Ni in various species of MnO2.
The micro-amount of nickel in MnO2, electrolytical and natural both, was determined by differential pulse polarography. NH4OH-NH4Cl was used as supporting electrolyte. It was found that the peak potential of Ni(II) reduction wave is -1.0V (vs. Ag-AgCl electrode). The presence of great amount of Mn(II) does not interfere in the trace nickel determination. the peak current relationship with the Ni2+ concentration presents a quite fine straight line. The differential pulse polarography is proved that it is a simple, reliable and acceptable method for determination of trace Ni in various species of MnO2.
