• 专利标题:   Method for detecting microcystin-LR in water, involves preparing graphene modified titanium dioxide nanotube arrays, followed by dropping microcystin-LR nucleic acid aptamer solution in nanotube arrays, and determining microcystin-LR.
  • 专利号:   CN106468681-A, CN106468681-B
  • 发明人:   LIU M, YU J, ZHAO G
  • 专利权人:   UNIV TONGJI, UNIV TONGJI
  • 国际专利分类:   G01N027/30
  • 专利详细信息:   CN106468681-A 01 Mar 2017 G01N-027/30 201727 Pages: 10 Chinese
  • 申请详细信息:   CN106468681-A CN10514844 20 Aug 2015
  • 优先权号:   CN10514844

▎ 摘  要

NOVELTY - A microcystin-LR detecting method involves preparing graphene modified titanium dioxide nanotube arrays. The graphene modified titanium dioxide nanotube arrays is dropped with prepared microcystin-LR nucleic acid aptamer aqueous solution to obtain microcystin-LR photoelectrochemical fitness sensor, followed by preparing different concentrations of microcystin-LR standard solution, applying bias, measuring photocurrent, drawing standard working curve, adding the sample containing microcystin-LR, and determining microcystin-LR concentration of the sample by combining the standard working curve. USE - Method for detecting microcystin-LR in water. ADVANTAGE - The method enables detecting microcystin-LR with high detecting sensitivity and high selectivity, in simple manner. DETAILED DESCRIPTION - A microcystin-LR detecting method involves ultrasonically dispersing copper(II) sulfate pentahydrate in ascorbic acid in tetrahydrofuran solution A, placing titanium dioxide nanotube arrays in dispersed tetrahydrofuran solution A, reacting under the protection of nitrogen, washing and drying to obtain graphene modified titanium dioxide nanotube arrays electrode. The graphene modified titanium dioxide nanotube arrays is dropped with prepared microcystin-LR nucleic acid aptamer aqueous solution, allowed to stand at room temperature to obtain microcystin-LR photoelectrochemical fitness sensor, followed by preparing different concentrations of microcystin-LR standard solution by adding microcystin-LR photoelectrochemical fitness sensor as working electrode of the three-electrode system, applying bias at room temperature, measuring photocurrent in the visible light excitation using the I-t curve method, drawing standard working curve by the logarithm of the change of the photocurrent density and the microcystin-LR standard solution concentration, adding the sample containing microcystin-LR to the three-electrode system to measure the photocurrent density, and determining microcystin-LR concentration of the sample to be tested by combining the standard working curve.