Enhanced fluorescent carbon dot, preparation method and application in cadmium ion detection
A fluorescent carbon dot and enhanced technology, applied in fluorescence/phosphorescence, chemical instruments and methods, nano-carbon, etc., can solve the problems of high biological toxicity, poor selectivity, and low sensitivity, and achieve low cytotoxicity, simple method, and high selective effect
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Embodiment 1
[0049] Grind 0.5 g of salicylic acid and 0.025 g of 5-amino-1,10-phenanthroline to mix well, then transfer the powder to a 25 mL crucible, raise the tube furnace temperature to 200 °C, The heating rate was 5°C / min, and the temperature was kept for 2h. After cooling to room temperature, the product was dissolved in ultrapure water, filtered with a 0.22 μm microporous membrane, the filtrate was put into a 3500Da dialysis bag, dialyzed for 48h, and the outer liquid was freeze-dried to obtain red fluorescent carbon dot powder.
[0050] The obtained red fluorescent carbon dot powder was dissolved in ultrapure water, dropped on an ultrathin copper grid, and its morphology was observed. Transmission electron microscope (TEM) image of carbon dots figure 1 As shown, it can be seen that the prepared carbon dot particles are uniformly dispersed, and the average particle size is 2.46 nm.
[0051] The prepared red fluorescent carbon dots were tested by ultraviolet spectrum, and the resul...
Embodiment 2
[0059] Weigh 0.5g of salicylic acid and 0.015g of 5-amino-1,10-phenanthroline powder and place them in a quartz mortar for thorough grinding. Transfer the uniformly mixed powder to a 25mL quartz crucible for calcination. The furnace temperature was raised to 200 °C for 2 h, and the heating rate was 5 °C / min. After cooling to room temperature, the obtained product was dissolved in ultrapure water, filtered through a 0.45 μm microporous membrane, and the filtrate was collected and dialyzed at 1000 Da for 24 h. Finally, the red fluorescent carbon dot powder is obtained by freeze-drying.
[0060] Using the method of Example 1 to detect the red fluorescent carbon dot powder prepared in this example, it can be found that the prepared red fluorescent carbon dot particles are uniformly dispersed, the maximum excitation wavelength is 450 nm, and the emission peak is located at 605 nm. 2+ High selectivity, strong anti-interference ability, low cytotoxicity, Cd 2+ The concentration of ...
Embodiment 3
[0062] Weigh 0.5g of salicylic acid and 0.05g of 5-amino-1,10-phenanthroline powder and place them in a quartz mortar for sufficient grinding, transfer them to a 25mL quartz crucible for calcination, and raise the temperature of the tube furnace to The reaction was carried out at 220 °C for 4 h, and the heating rate was 5 °C / min. After cooling to room temperature, the obtained product was dissolved in ultrapure water, filtered with a 0.22 μm microporous membrane, and the filtrate was collected and dialyzed at 3500 Da for 36 h. Finally, the red fluorescent carbon dot powder is obtained by freeze-drying.
[0063] Using the method of Example 1 to detect the red fluorescent carbon dot powder prepared in this example, it can be found that the prepared red fluorescent carbon dot particles are uniformly dispersed, the maximum excitation wavelength is 450 nm, and the emission peak is located at 605 nm. 2+ High selectivity, strong anti-interference ability, low cytotoxicity, Cd 2+ Th...
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