do Nascimento P C, Bohrer D, Tramontina J
Department of Chemistry, Federal University of Santa Maria, Brazil.
Analyst. 1997 Aug;122(8):835-8. doi: 10.1039/a700111h.
A method for the automated polarographic determination of sulfide in a gas-diffusion flow system was developed. The volatile sulfide, existing as a contaminant in parenteral amino acid solutions, was measured after gas diffusion using 0.1 mol l-1 NaOH solution as acceptor. The linear range of calibration, for measurements at a dropping-mercury electrode (DME), was from 5 to 100 micrograms of sulfide with r = 0.999 and RSD = 7.5% (n = 5) for 10 micrograms of sulfide. For measurements at the hanging mercury-drop electrode (HMDE), with a preconcentration time of 30 s, the linear range of calibration was from 0.9 to 20 micrograms of sulfide with r = 0.998 and RSD = 5.8% (n = 5) for 2 micrograms of sulfide. Detection limits of 59 and 11 micrograms l-1 at the DME and HMDE, respectively, were calculated and the recoveries of sulfide from spiked samples were 91.5-104.5%. Parameters that affect the sulfide determination using this method, such as the organic content of the matrix, pH, flow rate and sample size, were investigated.
开发了一种在气体扩散流动系统中自动极谱测定硫化物的方法。以0.1 mol l-1氢氧化钠溶液作为接受体,在气体扩散后测定存在于肠外氨基酸溶液中的挥发性污染物硫化物。在滴汞电极(DME)上进行测量时,校准的线性范围为5至100微克硫化物,对于10微克硫化物,r = 0.999,相对标准偏差(RSD)= 7.5%(n = 5)。在悬汞滴电极(HMDE)上进行测量时,预浓缩时间为30秒,校准的线性范围为0.9至20微克硫化物,对于2微克硫化物,r = 0.998,RSD = 5.8%(n = 5)。分别计算出在DME和HMDE上的检测限为59和11微克 l-1,加标样品中硫化物的回收率为91.5 - 104.5%。研究了影响使用该方法测定硫化物的参数,如基质的有机物含量、pH值、流速和样品量。