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作 者:Lingjuan YANG Shuiying GU Meng GE
机构地区:[1]School of Life Science and Chemistry,Tianshui Normal University
出 处:《Agricultural Biotechnology》2012年第3期59-61,共3页农业生物技术(英文版)
基 金:Supported by the National Natural Science Foundation of China(20275023)
摘 要:[ Objective] This study aimed to establish an electrochemiluminescence method for determining the trace molybdenum in plant seeds. [ Method ] The equipment used in this study consisted of an electrogenerated reagent system and a flow-injection chemiluminescence detection system. The optimal electric poten- tial, reagent acidity, flow rate of sample solution, as well as the concentration and alkalinity of luminal were screened to measure the trace molybdenum in plant seeds. [ Result I The unstable molybdenum (III) was on-line electrogenerated from molybdenum (VI) via controlled potential electrolysis technique using a home- made flow-through carbon electrolytic cell at the potential of -0.60 V (vs Ag/AgC1). The method allowed the determination of 5.0 × 10-10 _ 5.0 ×10-7 g/ml mo- lybdenum with a detection limit of 5 × 10 u g/ml molybdenum (VI). The relative standard deviation was 2.6% for the 1.0 × 10 -9 g/ml molybdenum solution in 11 measurements. [ Conclusion] Compared with the previous methods, this electrochemilum^nescence method not only improved the selectivity of the determina- tion, but also avoided the use of toxic reagent mercury.[ Objective] This study aimed to establish an electrochemiluminescence method for determining the trace molybdenum in plant seeds. [ Method ] The equipment used in this study consisted of an electrogenerated reagent system and a flow-injection chemiluminescence detection system. The optimal electric poten- tial, reagent acidity, flow rate of sample solution, as well as the concentration and alkalinity of luminal were screened to measure the trace molybdenum in plant seeds. [ Result I The unstable molybdenum (III) was on-line electrogenerated from molybdenum (VI) via controlled potential electrolysis technique using a home- made flow-through carbon electrolytic cell at the potential of -0.60 V (vs Ag/AgC1). The method allowed the determination of 5.0 × 10-10 _ 5.0 ×10-7 g/ml mo- lybdenum with a detection limit of 5 × 10 u g/ml molybdenum (VI). The relative standard deviation was 2.6% for the 1.0 × 10 -9 g/ml molybdenum solution in 11 measurements. [ Conclusion] Compared with the previous methods, this electrochemilum^nescence method not only improved the selectivity of the determina- tion, but also avoided the use of toxic reagent mercury.
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