Katano Hajime, Ueda Tadaharu
Faculty of Biotechnology, Fukui Prefectural University, Eiheiji, Fukui, Japan.
Anal Sci. 2011;27(10):1043-7. doi: 10.2116/analsci.27.1043.
New appropriate reaction system was found for spectrophotometric determination of phosphate anion. This spectrophotometric method is based on the color development due to the formation of yellow molybdophosphate anion in acidic ethylene glycol-water (EG-W) mixed solution containing Mo(VI) species. The solution containing e.g. 20 mM Na(2)MoO(4), 0.1 M HCl, and 40% (v/v) EG is colorless, and becomes immediately yellow by addition of phosphate anion. Thus the method is simple, rapid, and easy to carry out. Although Si(IV) species is well known to interfere with the determination of phosphate anion in many cases, the EG-W Mo(VI) solution remains colorless after addition of silicate anion at 1 mM level, indicating that no yellow molybdosilicate anion was formed in the EG-W solution. Under an optimized condition, the absorbance at e.g. 400 nm of the EG-W P(V)-Mo(VI) solution was proportional to the concentration of phosphate anion with good reproducibility, and the detection limit was 1 µM. Also the present method is less interfered by high concentrations of potassium and ammonium cations and oxidative nitrite anion as well as silicate anion.
发现了用于分光光度法测定磷酸根阴离子的新型合适反应体系。这种分光光度法基于在含有钼(VI)物种的酸性乙二醇 - 水(EG - W)混合溶液中形成黄色钼磷酸根阴离子而显色。例如,含有20 mM钼酸钠、0.1 M盐酸和40%(v/v)乙二醇的溶液是无色的,加入磷酸根阴离子后会立即变黄。因此该方法简单、快速且易于实施。虽然在许多情况下,硅(IV)物种众所周知会干扰磷酸根阴离子的测定,但在加入1 mM水平的硅酸根阴离子后,EG - W钼(VI)溶液仍保持无色,这表明在EG - W溶液中未形成黄色钼硅酸根阴离子。在优化条件下,例如EG - W磷(V) - 钼(VI)溶液在400 nm处的吸光度与磷酸根阴离子浓度成正比,具有良好的重现性,检测限为1 μM。此外,本方法受高浓度钾离子、铵离子、氧化性亚硝酸根阴离子以及硅酸根阴离子的干扰较小。