Glow-type chemiluminescent sensor based on hydrogel and its preparation method and application
A chemiluminescence and hydrogel technology, applied in chemiluminescence/bioluminescence, analysis by chemical reaction of materials, etc., can solve problems such as limited application, complex electrode modification process equipment and equipment, etc., to enhance chemiluminescence intensity , The effect of long chemiluminescence time and high sensitivity
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Embodiment 1
[0049] Example 1 ABEI / Co 2+ Synthesis of / CS hydrogel
[0050] In 15mL alkaline solution (mass ratio is LiOH: KOH: urea: H 2 (O=4.5:7:8:80.5) stirring and dispersing 0.4g chitosan powder, adding 0.6mL CoCl 2 (1mM) solution, stirred for 5 minutes, and refrigerated at -20°C until completely frozen. After thawing at room temperature, 1.5 mL of ABEI (10 mM) solution was added and stirred for 5 hours to uniformly disperse in the system to obtain ABEI / Co 2+ / CS hydrogel and store at 4 °C.
[0051] figure 2 A shows the synthetic ABEI / Co 2+ / CS SEM image of the hydrogel; the characteristic absorption peak of ABEI is located at the red line at 291nm, and the ultraviolet-visible absorption spectrum proves that ABEI is successfully wrapped in the hydrogel.
Embodiment 2
[0052] Example 2 ABEI / Co 2+ Synthesis of / CS hydrogel
[0053] In 15mL alkaline solution (mass ratio is LiOH: KOH: urea: H 2 (O=4.5:7:8:80.5) stirring and dispersing 0.4g chitosan powder, adding 0.6mL CoCl 2 (0.1 mM) solution, stirred for 5 minutes, and refrigerated at -20°C until completely frozen. After thawing at room temperature, add 1.5mL ABEI (4mM) solution and stir for 5 hours to be uniformly dispersed in the system to obtain ABEI / Co 2+ / CS hydrogel and store at 4 °C.
Embodiment 3
[0054] Example 3 Synthesis of MOF-Pt
[0055] First, weigh 0.2g of TCPP, 0.12g of AlCl 3 ·3H 2 The CTAB of O and 0.144g was dissolved in 20mL water, stirred for 10 minutes and placed in a 20mL reactor, then reacted at 180°C for 16 hours, after centrifuging at 3000rpm, the supernatant was centrifuged at 13000rpm to obtain a precipitate. The precipitate was washed twice with DMF, water and acetone, respectively, and then dried overnight in vacuum. Then, purple and black precipitates were obtained by vacuum drying at 150°C for 7 hours for further reaction. Then weigh 0.038g of precipitate and 0.064g of Cu(Ac) 2 It was dissolved in 8ml of DMF organic solvent, stirred for 10 minutes, then poured into a 20mL reaction kettle, and reacted at 100°C for 24 hours to obtain a red-black blocky precipitate. After centrifugation at 13000rpm, the precipitate was washed twice with DMF, water and acetone, and then dried in vacuo overnight to obtain product 1.
[0056] Finally, 0.5ml of H ...
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