采用催化过氧化氢氧化Ni(Ⅱ)-铬蓝黑R络合物光度法测定汞,通过优化对比实验,确定最佳反应条件为在pH4.12的HAc-NaAc缓冲溶液中,以2.00mL4g/L聚乙烯醇(PVA)作表面活性剂,5.00mLH2O2(1+9)溶液可氧化1.00mL0.00lmol/LNi^2+溶液与1.00mL0.400g/L铬蓝黑R溶液反应生成的Ni(II)-铬蓝黑R络合物,75℃水浴加热,汞对该反应具有明显催化作用。在波长571nm处催化体系和非催化体系的吸光度差值最大。Hg(Ⅱ)在0.1~2.0μg/L范围内符合朗格-比尔定律,检出限为3.2×10^-9g/L。经实际水体样本论证,本法可用于自然水体中痕量汞的直接测定。
A new catalytic kinetic spectrophotometric determination of trace mercury( 11 ) based on its catalytic oxidizing discoloration reaction of nickel( II )-palatine chrome black complex by 5.00 mL of 3.0% hydrogen peroxide with 2.00 mL of 0.4% pelyvinyl alcohol (PVA) as an activating agent in the presence of acetic acid-sodium acetate buffer solution of pH 4.12. The maximum absorbance difference of catalytic system and non-catalytic system appears at 571 um. The beer's law is well obeyed in the range of 0.1 - 2 μg/L for mercury, and the detection limit is 3.2 × 10^-9 g/L. The method is free from interference of common ions after extraction separation, and it has been applied to the determination of trace amounts of mercury in water.