Electrochemical sensor for sensitively detecting dopamine (DA) and uric acid (UA) simultaneously and preparation method
An electrochemical and dopamine technology is applied in the field of preparation of microwave exfoliated porous carbon modified glassy carbon electrodes, which can solve the problems of inability to detect dopamine and uric acid, difficulty in realizing trace detection, and high detection limit, and achieve a wide detection linear range and good conductivity. the effect of low detection limit
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Embodiment 1
[0036] A preparation method of a modified glassy carbon electrode, comprising:
[0037] Preparation of porous carbon exfoliated by microwave
[0038] First, synthesize graphene oxide by the Hummers method, and then use a microwave oven to heat the graphene oxide for 1 minute under the condition of 100W to obtain exfoliated graphene oxide carbon. Add 400 mg of microwave-exfoliated graphite oxide to 20 mL of 7 mol / L potassium hydroxide solution. The microwave-exfoliated graphite oxide / potassium hydroxide mixed solution was stirred for 24 hours, then filtered and dried, then activated at a high temperature of 800°C for 1 hour under an argon atmosphere, and then the sample was washed with deionized water and dried at 65°C. Finally, the pyrolyzed sample was heat-treated at 800°C for 2 hours in a vacuum atmosphere to obtain the prepared microwave-exfoliated porous graphitic carbon. Microwave exfoliation of porous carbon is a kind of sheet-like structure ( image 3 a and b), with ...
Embodiment 2
[0042] Optimization of electrode dispensing volume
[0043] Repeat Example 1, use a pipette gun to pipette 2, 3, 4, 5, 6, 7, 8, 9 μL of the electrode modification solution obtained in Example 1, drop-coat it on the surface of the polished glassy carbon electrode, and apply the obtained modified electrode For the detection of 10μmol / L dopamine and uric acid. The oxidation peak currents of dopamine and uric acid both increased first and then decreased with the increase of the dripping amount, and the peak current reached the maximum when the dripping amount was 5 μL.
Embodiment 3
[0044] The simultaneous selective detection of embodiment 3 dopamine and uric acid:
[0045] One end of the glassy carbon electrode, reference electrode, and counter electrode prepared by microwave exfoliation of porous carbon materials prepared in Example 2 were immersed in 0.1 mol / L of uric acid containing 10 μmol / L, 10 μmol / L dopamine and 1000 μmol / L ascorbic acid respectively. In phosphate buffer solution (pH=7.0), the other ends of the three electrodes were connected to the electrochemical workstation. Cyclic voltammetry was selected on the electrochemical workstation, the scan rate was set to 100mV / s, and the scan range was set to -0.2V-0.8V.
[0046] Run the cyclic voltammetry technique on the electrochemical workstation, and record the current-voltage curve by the electrochemical workstation, such as Figure 4 As shown, the cyclic voltammetry curves of dopamine and uric acid are obtained, from Figure 4 It can be seen that compared with the bare glassy carbon electro...
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