Carbon nanotube surface molecularly imprinted polymer as well as preparation method and application thereof
A technology of surface molecular imprinting and carbon nanotubes, which is applied in the direction of material electrochemical variables, can solve problems such as unfavorable enterprise and social development, a large amount of pollutants, and environmental hazards, so as to improve conductivity and current response speed, take a long time, highly sensitive effect
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Embodiment 1
[0085] Example 1 Preparation of Molecularly Imprinted Polymer on Carbon Nanotube Surface
[0086] 1. Preparation of molecularly imprinted polymers on the surface of carbon nanotubes
[0087] The preparation process of molecularly imprinted polymers on the surface of carbon nanotubes is as follows: figure 1 As shown, it specifically includes the following steps:
[0088] (1) Purification of carboxylated multi-walled carbon nanotubes
[0089] In order to remove a small amount of amorphous carbon and metal impurities in carboxylated multi-walled carbon nanotubes (CNTs), the CNTs-COOH is purified. The purification method is:
[0090] In a 100 mL round bottom flask, 40.0 mL H 2 O, 9.28mL HNO 3 Mix well, then add 2.0g CNTs-COOH, and reflux at 85°C for 48h. After filtering, the CNTs-COOH was washed with deionized water to neutrality, and dried in vacuum at 60°C for 12 hours, and set aside.
[0091] (2) Synthesis of silica-coated multi-walled carbon nanotubes
[0092] Weigh 250...
Embodiment 2
[0112] The preparation of embodiment 2 electrochemical sensor
[0113] 1. Preparation of electrochemical sensors
[0114] (1) The naked glassy carbon electrode (GCE, diameter 3mm) is sequentially coated with 0.3μm, 0.05μm Al 2 o 3 Powder suspension polishing treatment, and then with absolute ethanol, ddH 2 O ultrasonic (53KHz) cleaning, each 10min, finally place room temperature to dry, stand-by;
[0115] (2) Take 20.0mg γ-MAPS / CNTsSiO 2 -MIPs were added to 1mL of 0.5% chitosan solution, 53KHz ultrasonic 60min, so that the two were evenly mixed to obtain a mixed solution; then take 5.0 μL of the mixed solution and apply it on the surface of the bare glassy carbon electrode treated in step (1), Dry at room temperature for 6 hours to obtain the imprinted electrode (γ-MAPS / CNTsSiO 2 -MIPs / GCE);
[0116](3) Use the imprinted electrode of step (2) as the working electrode, the saturated calomel electrode as the reference electrode, the platinum electrode as the counter electr...
Embodiment 3
[0147] Embodiment 3 The detection of the actual sample by the electrochemical sensor
[0148] In order to investigate the detection feasibility of the electrochemical sensor of the present invention, the actual sample rutin tablets were tested.
[0149]First, use a mortar to grind the commercially available rutin tablets, and then use ethanol to ultrasonically dissolve it completely to obtain a rutin tablet solution; take an appropriate amount of the upper layer of the rutin tablet solution with PBS buffer solution (pH4.5) Dilute to 5 mL. Then, the imprinted electrode was immersed in the above diluent, stirred and adsorbed for 7 minutes, and DPV detection was performed. Each sample was tested 5 times in parallel, and the average value was taken. The detection results are shown in Table 2.
[0150] Table 2
[0151]
[0152] It can be seen from Table 2 that the detection value of the imprinted electrode is basically consistent with the marked value, the recovery rate is 99....
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