Preparation method of carbon nanocage fluorescent probe and application thereof in Fe<3+> detection
The technology of fluorescent probe and carbon nano-cages is applied in the field of preparation and application of fluorescent probe, which can solve the problems of difficult operation and complicated preparation method, and achieve the effects of low cost, simple and convenient operation, and simple and controllable preparation process.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0045] Embodiment 1: Preparation of carbon nanocage fluorescent probe
[0046]The conger eel baked at 180°C for 30 minutes was soaked in absolute ethanol with 1ml of ethanol per gram of fish for 15 hours to roughly extract the carbon nanocages; until the ethanol was completely removed by rotary evaporation, three Chloromethane was redissolved, extracted three times, and degreased until the aqueous phase solution was clear and transparent. The crude aqueous phase solution was subjected to G25 dextran gel column chromatography, and the collected fluorescence intensity was higher than 80 (excitation wavelength = 330nm, emission wavelength = 390nm ) part, freeze-dried to obtain a powdery substance.
[0047] It can be detected by a transmission electron microscope that it has a hollow carbon nanocage structure with multiple ring-shaped shell layers and a diameter of less than 100 nm.
[0048] The carbon nanocage fluorescence yield is measured by a known formula, the formula is: Φ ...
Embodiment 2
[0051] Embodiment 2: Preparation of carbon nanocage fluorescent probe
[0052] The conger eel that had been baked at 280°C for 15 minutes was soaked in absolute ethanol with 1ml of ethanol per gram of fish for 12 hours to roughly extract the carbon nanocages; until the ethanol was completely removed by rotary evaporation, three Chloromethane was redissolved, extracted three times, and degreased until the aqueous phase solution was clear and transparent. The crude aqueous phase solution was subjected to G25 dextran gel column chromatography, and the collected fluorescence intensity was higher than 80 (excitation wavelength = 330nm, emission wavelength = 390nm ) part, freeze-dried to obtain a powdery substance.
[0053] It can be detected by a transmission electron microscope that it has a hollow carbon nanocage structure with multiple ring-shaped shell layers and a diameter of less than 100 nm.
[0054] The carbon nanocage fluorescence yield is measured by a known formula, the...
Embodiment 3
[0057] Embodiment 3: Preparation of carbon nanocage fluorescent probe
[0058] Soak the whole turbot roasted at 230°C for 30 minutes in absolute ethanol, leaching with 1ml of ethanol per gram of fish for 12 hours, and extract the carbon nanocages roughly; until the ethanol is completely removed, use Trichloromethane redissolution, extraction three times, degreasing, until the aqueous phase solution is clear and transparent, the crude aqueous phase solution is subjected to G25 dextran gel column chromatography, and the collected fluorescence intensity is higher than 80 (excitation wavelength=330nm, emission wavelength= 390nm) part was lyophilized to obtain a powdery substance.
[0059] It can be detected by a transmission electron microscope that it has a hollow carbon nanocage structure with multiple ring-shaped shell layers and a diameter of less than 100 nm.
[0060] The carbon nanocage fluorescence yield is measured by a known formula, the formula is: Φ 1 = Φ 2 I 1 A 2...
PUM
| Property | Measurement | Unit |
|---|---|---|
| concentration | aaaaa | aaaaa |
| wavelength | aaaaa | aaaaa |
| diameter | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
Login to View More 


