A modified electrode and a method for electrochemically detecting sulpiride
An electrochemical, glassy carbon electrode technology, applied in the electrochemical detection of Sulpiride, α-MoO3 nanorod modified glassy carbon electrode field, can solve the problems of low efficiency of Sulpiride, long analysis time, high catalytic activity, etc., to achieve strong application value , The effect of high electrochemical activity and high sensitivity
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Embodiment 1
[0024] Preparation of α-MoO 3 Nanorod modified glassy carbon electrode:
[0025] (1) α-MoO 3 Preparation of powder: ultrasonically disperse anhydrous sodium molybdate and hydrochloric acid in deionized water at a molar ratio of 1:3, then transfer the dispersion to a polytetrafluoroethylene high-pressure reactor, and place the reactor in a heating device 1 h at 150°C, cooled naturally to room temperature, filtered, dried, and then placed in a tube furnace and calcined at 350°C for 1 h in an air atmosphere to obtain α-MoO 3 powder;
[0026] (2) Glassy carbon electrode pretreatment: the glassy carbon electrode was polished with 0.1 μm and 0.05 μm alumina powder for 2 minutes in turn, and polished to a mirror surface, and the polished glassy carbon electrode was ultrasonically cleaned with acetone and deionized water for 3 minutes, respectively, to obtain Pretreated glassy carbon electrodes;
[0027] (3)α-MoO 3 Nanorod-modified glassy carbon electrodes: using prepared α-MoO ...
Embodiment 2
[0029] Preparation of α-MoO 3 Nanorod modified glassy carbon electrode:
[0030] (1) α-MoO 3 Powder preparation: ultrasonically disperse anhydrous sodium molybdate and hydrochloric acid in deionized water at a molar ratio of 1:7, then transfer the dispersion to a polytetrafluoroethylene high-pressure reactor, and place the reactor in a heating device In 190°C, hydrothermal reaction was carried out for 4h, naturally cooled to room temperature, filtered, dried, then placed in a tube furnace, and calcined at 500°C for 4h in an air atmosphere to obtain α-MoO 3 powder;
[0031] (2) Glassy carbon electrode pretreatment: the glassy carbon electrode was polished with 0.1 μm and 0.05 μm alumina powder for 2 minutes in turn, and polished to a mirror surface, and the polished glassy carbon electrode was ultrasonically cleaned with acetone and deionized water for 3 minutes, respectively, to obtain Pretreated glassy carbon electrodes;
[0032] (3)α-MoO 3 Nanorod-modified glassy carbon...
Embodiment 3
[0034] α-MoO 3 Preparation of nanorod modified glassy carbon electrodes:
[0035] (1) α-MoO 3 Preparation of powder: ultrasonically disperse anhydrous sodium molybdate and hydrochloric acid in deionized water at a molar ratio of 1:5, then transfer the dispersion to a polytetrafluoroethylene high-pressure reactor, and place the reactor in a heating device in 170°C for 2h, cooled to room temperature naturally, filtered, dried, and then placed in a tube furnace, calcined at 400°C for 2h in an air atmosphere to obtain α-MoO 3 powder;
[0036] (2) Glassy carbon electrode pretreatment: the glassy carbon electrode was polished with 0.1 μm and 0.05 μm alumina powder for 2 minutes in turn, and polished to a mirror surface, and the polished glassy carbon electrode was ultrasonically cleaned with acetone and deionized water for 3 minutes, respectively, to obtain Pretreated glassy carbon electrodes;
[0037] (3)α-MoO 3 Nanorod-modified glassy carbon electrodes: using prepared α-MoO ...
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