Method for determining nitrate and nitrite ions in cigarette tipping paper
A technology of nitrite ion, cigarette tipping paper, applied in the direction of measuring device, material separation, instrument, etc., to achieve the effect of simple operation, prolonged service life and good repeatability
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Embodiment 1
[0031] Such as figure 1 The flow shown is to determine the content of nitrate and nitrite ions in cigarette tipping paper.
[0032] (1) Preparation of standard working solution: Standard solutions of nitrate and nitrite ions were purchased from the National Material Center, the concentrations were: 1000 μg / mL, specific preparation of standard working solutions of nitrate and nitrite ions with concentration gradients The method is: pipette 1 mL of 1000 μg / mL NO 3 - and NO 2 - Standard solution, dilute to 100mL volumetric flask with deionized water to obtain NO concentration of 10μg / mL 3 - and NO 2 - For the primary standard solution, take 0.1mL, 0.2mL, 0.5mL, 1.0mL, 2.0mL, and 5.0mL primary standard solution respectively, and dilute it to a 10mL volumetric flask with deionized water to obtain a standard solution with the following concentration: 0.1mg / L, 0.2mg / L, 0.5mg / L, 1.0mg / L, 2.0mg / L, 5.0mg / L. The obtained standard working solution should be prepared and used imm...
Embodiment 2
[0051] The method of present embodiment measuring nitrate and nitrite ion content in cigarette tipping paper is as follows:
[0052] 1. Preparation of sample solution: Accurately cut a sample of cigarette tipping paper (should include a single side) with a length of 200mm and a width of 40mm. Place the cut sample on a balance and weigh it to an accuracy of 0.1mg, and use scissors to cut the sample into fragments no larger than 0.5cm×0.5cm, place the fragments in a 100mL Erlenmeyer flask with a stopper, and accurately add 40mL of deionized water, placed in a water bath at 60°C for 40 minutes, cooled to room temperature, and the supernatant was passed through a 0.22 μm water-based syringe filter and a C18 column (discard the first 3 mL) to obtain a sample solution, which was analyzed by IC.
[0053] 2, adopt the chromatographic condition analysis sample solution of embodiment 1;
[0054] 3, the chromatographic peak area that records nitrate and nitrite ion is brought into the s...
Embodiment 3
[0059] The present embodiment is specifically implemented as follows to the repeatability of the inventive method and the recovery rate of standard addition:
[0060] Select different samples according to the pretreatment method, measure the background value, add a certain concentration of mixed standard solution, and perform IC analysis after treatment according to the pretreatment method. Determination of the chromatographic analysis conditions is the same as in Example 1. According to the analysis results, the recovery of nitrate and nitrite ions in the tipping paper for cigarettes of this method and the relative standard deviation (n=5) of the measured value after the addition of the standard are calculated. The results As shown in Table 4:
[0061] Table 4 The results of standard addition recovery and relative standard deviation (n=5)
[0062]
[0063] It can be seen from Table 4 that NO 3 - The average recovery rate of 97.6%, NO 2 - The average recovery rate of 1...
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