Yang Bo, Zhou Li-qiong, Yin Jia-yuan
Department of Physics, Yuxi Teachers College, Yuxi 653100, China.
Guang Pu Xue Yu Guang Pu Fen Xi. 2004 Sep;24(9):1110-2.
Based on the color reaction of mercurywith 5-(2-hydroxy-4-sulfo-5-chlorophenol-1-azo)-thiorhodanine (HSTC) and the solid phase extraction of the colored complex with C18 cartridge, a new method for the determinations microg x L(-1) level of mercury was studied. In the presence of pH 3.6 HAc-NaAc buffer solution. HSTC reacted with mercury (II) to form a stable 2:1 complex. This complex was enriched by solid phase extraction with C18 cartridge and the retained complex from cartridge was eluted with DMF. An enrichment factor of 80 was achieved. In the measured solution, the molar absorptivity was 6.24 x 10(4) L x moL(-1) x cm(-1) at 545 nm. Beer's law was obeyed in the range of 0-1.5 microg x mL(-1). This method was applied to the determination of mercury in water. The relative standard devitions were 1.8%-2.2% and the recoveries were 93%-106%. The results are satisfactory.
基于汞与5-(2-羟基-4-磺基-5-氯苯酚-1-偶氮)-硫代罗丹宁(HSTC)的显色反应以及用C18小柱对有色配合物进行固相萃取,研究了一种测定微克每升水平汞的新方法。在pH 3.6的HAc-NaAc缓冲溶液存在下,HSTC与汞(II)反应形成稳定的2:1配合物。该配合物用C18小柱进行固相萃取富集,小柱上保留的配合物用N,N-二甲基甲酰胺洗脱。富集倍数达到80。在测定溶液中,545 nm处的摩尔吸光系数为6.24×10⁴ L·mol⁻¹·cm⁻¹。在0-1.5微克每毫升范围内符合比尔定律。该方法用于水中汞的测定。相对标准偏差为1.8%-2.2%,回收率为93%-106%。结果令人满意。