Method for rapidly determining total nitrogen content in water by using resorcinol
A technology for rapid determination of resorcinol, which is applied in the preparation of test samples, measurement of color/spectral characteristics, analysis through chemical reactions of materials, etc., which can solve the problems of low test efficiency
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Embodiment 1
[0060] Use different concentrations of total nitrogen standard solutions to simulate water samples, and operate according to the above-mentioned method for rapidly determining total nitrogen content in water using resorcinol.
[0061] When the sample is digested, take 1ml sample in the colorimetric tube, first add 1ml digestion solution to the colorimetric tube, digest at 110°C for 10 minutes, then add 1ml digestion solution to the colorimetric tube, and digest at 110°C for 10 minutes min;
[0062]Then use a pipette to pipette 1.0ml of the digested solution into a 10ml non-color tube, add 1ml of 0.5% resorcinol and 3ml of concentrated sulfuric acid, shake and mix thoroughly; In a cuvette, measure the absorbance at a wavelength of 365 nm.
[0063] Two sets of tests were carried out, and the experimental data are as follows:
[0064]
Embodiment 2
[0066] The difference between the operation and Example 1 is that when the sample is digested, 2ml of digestion solution is added at one time, and it is digested at 110°C for 20 minutes; other operations are the same as in Example 1.
[0067] Two sets of tests were carried out, and the experimental data are as follows:
[0068]
[0069] By comparing the experimental data of Example 1 and Example 2, it can be seen that the digestion solution is added twice, and the sample is digested twice, and the curve is more linear. This is because the digestion solution is added twice, and the stability of the reaction is better.
Embodiment 3
[0071] The difference between the operation and Example 1 is that when the sample is digested, take 1ml of the sample in the colorimetric tube, first add 1ml of digestion solution to the colorimetric tube, digest it at 110°C for 10 min, and then add it to the colorimetric tube 1ml of digestion solution was digested at 110°C for 5min; then the absorbance of the sample was measured.
[0072] Two sets of experiments were carried out, and the experimental data were recorded as follows:
[0073]
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