Method of detecting hexavalent chromium by nitrogen-phosphorus doped carbon quantum dot probe
A carbon quantum dot and probe detection technology, applied in the field of hexavalent chromium detection, can solve problems such as inaccurate detection results, and achieve the effects of strong anti-interference ability, high sensitivity and strong electrical polarity
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Embodiment 1
[0037] A method for detecting hexavalent chromium using nitrogen and phosphorus doped carbon quantum dot probes, comprising the following steps:
[0038] Step 1, using a PBS buffer solution with a pH of 7.4 to prepare a nitrogen-phosphorus-doped carbon quantum dot solution with a concentration of 0.5 mg / mL, and using a PBS buffer solution with a pH of 7.4 to prepare a plurality of hexavalent chromium standard solutions with different concentrations, the hexavalent chromium The concentrations of the chromium standard solution are: 0, 1×10 -6 mol / L, 3×10 -6 mol / L, 5×10 -6 mol / L, 7×10 -6 mol / L, 9×10 -6 mol / L, 1.2×10 -5 mol / L, 1.5×10 -5 mol / L, 1.8×10 -5 mol / L, 2.1×10 -5 mol / L, 2.4×10 -5 mol / L, 2.7×10 -5 mol / L, 3.0×10 -5 mol / L, 3.3×10 -5 mol / L, 3.6×10 -5 mol / L, 3.9×10 -5 mol / L, 4.2×10 - 5 mol / L, 4.5×10 -5 mol / L, and 4.8×10 -5 mol / L, measure 19 parts of nitrogen-phosphorus-doped carbon quantum dot solution with a volume of 3ml, add a part of hexavalent chromium stan...
Embodiment 2
[0041] The determination procedure is the same as in Example 1, wherein the difference is the preparation method of nitrogen and phosphorus doped carbon quantum dots in step one, the preparation method of nitrogen and phosphorus doped carbon quantum dots solution, the preparation method of hexavalent chromium standard solution, and the preparation method containing hexavalent chromium The pretreatment of the solution to be tested of valence chromium is different, specifically as follows:
[0042] The preparation method of nitrogen and phosphorus doped carbon quantum dots is specifically as follows:
[0043] S1. Crush the hydrotalcite through a 120-mesh sieve, place it in tartaric acid, and heat it in a water bath at 30°C, 60°C, 90°C, and 30°C. The water bath time is 10min, 20min, 30min, and 10min, respectively. Wash the first precipitate with deionized water for 3 times, put it in the carbon tetrachloride solution of soybean lecithin and ultrasonically treat it for 20-30 minut...
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