Measurement of kinetic temperature and terminal velocity for argon atom and calcium ionin inductively coupled plasma mass spectrometry
MA Hai-bin1, SUN Zi-jie2
1. College of Chemistry, Chemical & Environmental Engineering, Weifang University, Weifang 261061, China; 2. Institute for Environmental Reference Materials, Ministry of Environmental Protection, Beijing 100029, China
Abstract:In order to guarantee the optimal detection property of inductively coupled plasma mass spectrometry (ICP-MS), the different analytical ions should pass the sampling interface efficiently and continuously. Therefore, the understanding of non-ideal transfer behaviors of ions on the sampling interface was very important. The measurement equipment of kinetic temperature and terminal velocity of various particles after the sampling cone of ICP-MS was established based on the Doppler frequency shift and high resolution laser induced fluorescence technologies. It was defined that the maximum fluorescence response intersection of calcium ion between horizontal and vertical directions was the zero point of calibration. The changes of terminal velocity and kinetic temperature of argon atom and calcium ion were calculated and compared. The results showed that the terminal velocity of calcium ion on vertical and horizontal directions of plasma torch tube was higher than that of neutral argon atom, indicating the acceleration of charged particle after sampling cone. The ambipolar diffusion in electric field and the acceleration of charged particles resulted in the more deviation from center axis of plasma. Therefore, it was more difficult to reach the skimmer cone. The experimental results could provide data support for the calculation of transmission efficiency on sampling interface and the development of related simulation model.
马海斌, 孙自杰. 电感耦合等离子体质谱仪中氩原子和钙离子的动力学温度及终端移动速率测量[J]. 冶金分析, 2015, 35(8): 7-11.
MA Hai-bin, SUN Zi-jie. Measurement of kinetic temperature and terminal velocity for argon atom and calcium ionin inductively coupled plasma mass spectrometry. , 2015, 35(8): 7-11.
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