Zhai Qing-Zhou, Zhang Xiao-Xia, Liu Qing-Zhou
Research Center for Nanotechnology, Changchun University of Science and Technology, Weixing Road, Changchun 130022, China.
Spectrochim Acta A Mol Biomol Spectrosc. 2006 Sep;65(1):1-4. doi: 10.1016/j.saa.2005.07.080. Epub 2005 Dec 13.
A new catalytic kinetic spectrophotometric method was proposed for determining trace oxalic acid based on the catalytic effect of oxalate on the oxidation of potassium dichromate with rhodamin B in 0.10 M of sulfuric acid. Good linearity is obtained over the concentration range 0.40-6.0 microg/mL of oxalic acid. After the reactions of the catalytic and non-catalytic systems were terminated by using 2.00 mL of 4 M sodium hydroxide solution, they can be stable for 3 h at room temperature. The apparent activation energy of the catalytic reaction is 12.44 kJ/mol. The effect of 50 coexisting substances was observed. The method was used to determine trace oxalic acid in tea, spinach and urine samples with satisfactory results.
基于在0.10 M硫酸介质中,草酸根对重铬酸钾氧化罗丹明B的催化作用,提出了一种测定痕量草酸的催化动力学分光光度法。草酸浓度在0.40 - 6.0 μg/mL范围内具有良好的线性关系。用2.00 mL 4 M氢氧化钠溶液终止催化和非催化体系的反应后,它们在室温下可稳定3 h。催化反应的表观活化能为12.44 kJ/mol。考察了50种共存物质的影响。该方法用于测定茶叶、菠菜和尿液样品中的痕量草酸,结果令人满意。