Process for producing low-toxicity fluorescent carbon point
A technology of fluorescent carbon dots and low toxicity, applied in the fields of chemistry and material science, can solve the problems of wide half-peak width of fluorescence spectrum, low fluorescence quantum yield, difficult separation of carbon dots, etc., and achieves low preparation cost, simple instrument and raw materials. Inexpensive effects from a wide range of sources
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Embodiment 1
[0015] (1) Cut multiple strands of carbon fiber into 4-5cm length, fix one end on the spectral pure graphite electrode with sealing glue, and rinse with ultrapure water.
[0016] (2) Put the cleaned carbon fiber electrode into a platinum beaker containing about 1 mol of sodium dihydrogen phosphate solution with a pH of 4.5, using the platinum beaker electrode as the auxiliary electrode, and the saturated calomel electrode (SCE) as the reference The electrode was electrolytically oxidized at a constant potential of 2V relative to the saturated calomel electrode for 120 minutes.
[0017] (3) Rinse the oxidized carbon fiber electrode with ultrapure water, usually until the rinsed aqueous solution is colorless, and collect the rinsed aqueous solution.
[0018] (4) Combine the sodium dihydrogen phosphate solution in (2) and the aqueous solution in (3), and centrifuge at RCF 28000g for 0.5-1 hour. Collect the supernatant and remove the precipitate.
[0019] (5) Ultrafiltration of the co...
Embodiment 2
[0021] (1) The spectral pure graphite electrode is ultrasonically cleaned in absolute ethanol and ultrapure water in sequence, and dried by nitrogen;
[0022] (2) Put the cleaned spectral pure graphite electrode into a platinum beaker containing a 0.1mol / L disodium hydrogen phosphate solution with a pH of 10.2, using the platinum beaker electrode as the auxiliary electrode, and the saturated calomel electrode (SCE ) Is the reference electrode, electrolytic oxidation is constant potential at a positive 9V potential relative to the saturated calomel electrode for 60 minutes.
[0023] (3) Rinse the oxidized spectral pure graphite electrode with ultrapure water, usually until the aqueous solution after the rinsing is colorless, and collect the aqueous solution after the rinsing.
[0024] (4) Combine the disodium hydrogen phosphate solution in (2) and the aqueous solution in (3), and centrifuge at RCF 28000g for 0.5-1 hour. Collect the supernatant and remove the precipitate.
[0025] (...
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