Sampling device used for analyzing polyaromatic hydrocarbon samples at real time in on-line mass spectrum
A real-time analysis and sampling device technology, applied in the field of time-of-flight mass spectrometry, can solve the problems of low saturated vapor pressure, sample gas condensation, serious memory effect, etc., and achieve stable temperature control, accurate quantification, and broad application prospects
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Embodiment 1
[0037] For the examination of the quantitative performance of the sampling device of the present invention, a pyrene sample is used to configure sample gases with different concentrations for detection. When configuring the sample gas, first use n-hexane as a solvent to dissolve a certain amount of pyrene sample, and then use high-purity nitrogen as a carrier gas to prepare 10ppm, 5ppm, 2.5ppm, and 1.25ppm sample gases at a high temperature of 200°C. During sampling, the flow rate of the sample gas is 200ml / min, and the temperature of the sampling pipeline is kept at 200°C. The time-of-flight mass spectrometer adopts vacuum ultraviolet lamp ionization, and the mass spectrometry signal of the obtained pyrene samples at each concentration is between figure 2 given in. image 3 It is the relationship curve between the integrated intensity of the mass spectrum signal peak area and the sample concentration at different concentrations of the pyrene sample, and the R value after fi...
Embodiment 2
[0039] For the examination of the memory effect of the sampling device of the present invention, a trichlorobenzene sample is used to configure a relatively large concentration of sample gas for detection. When configuring the sample gas, put the weighed trichlorobenzene solid sample in a certain amount of high-purity nitrogen gas, and completely volatilize the trichlorobenzene solid sample at a high temperature of 200°C to make a 100ppm sample gas. During sampling, the flow rate of the sample gas is 200ml / min, and the temperature of the sampling pipeline is kept at 200°C. The time-response curve of the obtained trichlorobenzene sample is as follows: Figure 4 As shown, the signal peak area integral of the trichlorobenzene sample gas dropped to a stable background noise level within 50 seconds after the injection was stopped, basically eliminating the memory effect and showing good time response characteristics.
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