Different carbon paste electrodes (CPEs) were investigated for their a
bility to act directly as supports for mercury films formed ''in situ'
' by electrodeposition. A CPE, containing tricresyl phosphate as a pas
ting liquid, was found to be especially suitable for this purpose. The
mercury film on this support exhibited a more negative potential limi
t than mercury films deposited onto common carbon pastes or glassy car
bon. Thus, the mercury film electrode (MFE) with the tricresyl phospha
te-based carbon paste support proved to be advantageous for differenti
al pulse anodic stripping voltammetry (DPASV) of Zn(II). The effects o
f various supporting electrolytes and nf the concentration of Hg(II) i
ons on the response of zinc, were studied in detail together with an o
ptimization of voltammetric parameters. Interferences from metal ions
such as Ni(II), Co(II), Mn(II), and Cu(II), were also investigated. Fo
r quantitative evaluations, Zn(II) was accumulated from a 0.1 M ammoni
a buffer containing 2 x 10(-5) M Hg(II), a with an accumulation potent
ial of -1.5 V (vs. Ag/AgCl). The current response of Zn(II) was linear
for a concentration range from 2 x 10(-) to 2 x 10(-5) mol/L with a d
etection limit of 1 x 10(-) mol/L (accumulation time 180 seconds). The
method was applied to the determination of Zn(II) in drinking water a
nd deionized water.