do Nascimento P C, Bohrer D, de Carvalho L M
Department of Chemistry, Federal University of Santa Maria, Brazil.
Analyst. 1998 May;123(5):1151-4. doi: 10.1039/a708675j.
The report describes a method for the automated polarographic determination of cyanide as tetracyanonickelate (II) anion complex in a gas-diffusion flow system. The volatile cyanide, existing in whole blood, plasma and urine samples, was measured after gas-diffusion using 8 x 10-5 mol l-1 hexaaminenickel solution as acceptor. The linear range of calibration, for measurements at the hanging mercury-drop electrode (HMDE), was from 0.1 to 2.0 micrograms cyanide with r = 0.998. The RSD was, respectively, 3.4 and 1.2% (n = 5) for 0.4 microgram cyanide measured with and without the flow-system configuration. Detection limits of 7.4 microgram l-1 were calculated using the flow system and the method was compared with the classical method using Cavet flasks. Parameters that affect the cyanide determination in the proposed method, such as acceptor solution, pH, flow rate and temperature, were investigated.
该报告描述了一种在气体扩散流动系统中自动极谱法测定氰化物的方法,氰化物以四氰合镍(II)阴离子络合物形式存在。使用8×10⁻⁵ mol l⁻¹六氨合镍溶液作为受体,通过气体扩散后测定全血、血浆和尿液样品中存在的挥发性氰化物。在悬汞滴电极(HMDE)上进行测量时,校准的线性范围为0.1至2.0微克氰化物,r = 0.998。在有和没有流动系统配置的情况下,测定0.4微克氰化物时的相对标准偏差分别为3.4%和1.2%(n = 5)。使用流动系统计算出的检测限为7.4微克 l⁻¹,并将该方法与使用凯氏烧瓶的经典方法进行了比较。研究了影响所提出方法中氰化物测定的参数,如受体溶液、pH值、流速和温度。