Analysis device and analysis method for quantitatively analyzing fluid inclusion water
A technique for quantitative analysis of fluid inclusions, applied in measuring devices, analyzing materials, and material analysis through electromagnetic means, can solve problems such as neglect, increase the uncertainty of interpretation, and uneven distribution of fluid inclusions
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Embodiment 1
[0055] The present invention adopts such as figure 1 and figure 2 The analysis device for the quantitative analysis of fluid inclusion water shown in the analysis, the analysis device for quantitative analysis of fluid inclusion water includes a heating furnace 10 and a quadrupole mass spectrometer 14, and the heating furnace 10 is used to analyze the fluid inclusions in the quartz glass tube 11 The sample is heated, and the quadrupole mass spectrometer 14 is used for quantitative analysis of the fluid inclusions in the quartz glass tube 11. A VLV needle valve 13 is arranged on the connecting pipeline at one end of the quadrupole mass spectrometer 14, and a VLV needle valve 13 Connect with SV1 gas control valve 7, SV2 gas control valve 5, SV3 gas control valve 12 respectively through communication pipeline, quantitative analysis component 1 is connected with SV3 gas control valve 12 through communication pipeline 9, quantitative analysis component 1 comprises collection tube ...
Embodiment 2
[0066] Step 1: Sample pretreatment: select a jadeite sample with a purity greater than 99%, a particle size of 60-80 mesh, and a sample size of more than 200 mg. The jadeite sample is jadeite quartzite collected from the ultra-high pressure metamorphic belt of the Dabie Mountains. Separate the jadeite single mineral that needs to be determined from the rock, and select the jadeite single mineral crystal without inclusions and no degeneration under the binocular lens; put the jadeite single mineral crystal into a 100ml beaker, add 50ml (1:1) HCl, heated on the electric heating plate, the heating temperature is 90 ° C, the heating time is 1 hour, overnight, pour out the acid the next day, wash the sample with pure water several times, ultrasonically shake for 10 minutes, and then rinse repeatedly with deionized water. The samples were dried in an oven at 80°C for later use.
[0067] Step 2: Draw a standard working curve: Accurately pipette 0, 0.5, 1, and 2 μL of high-purity wate...
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