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Direct solid atomic emission spectrometric analysis of metal samples by an argon microwave plasma torch coupled to spark ablation
Institution:1. Department of Physics, University of Azad, Jammu & Kashmir, Muzaffarabad, Pakistan;2. University of Pelita Harapan, 1100 M.H. Thamrin Boulevard, Lippo Village, Tangerang 15811, Indonesia;3. Department of Computer Engineering, Bina Nusantara University, 9 K.H. Syahdan, Jakarta 14810, Indonesia;4. Faculty of Mathematics and Natural Sciences, Syiah Kuala University, Darussalam, Banda Aceh 23111, Indonesia;5. Faculty of Mathematics and Natural Sciences, Diponegoro University, Tembalang, Semarang 50275, Indonesia;6. Faculty of Mathematics and Natural Sciences, Jakarta State University, 10 Rawamangun, Jakarta, Indonesia;7. Krida Wacana Christian University, Jakarta 11470, Indonesia;8. Faculty of Mathematics and Natural Sciences, Udayana University, Kampus Bukit Jimbaran, Denpasar 80361, Bali, Indonesia;9. Research Center of Maju Makmur Mandiri Foundation, 40/80 Srengseng Raya, Jakarta 11630, Indonesia;10. Fukui Science Education Academy, Takagi Chuou 2 choume, Fukui 910-0804, Japan;11. Physics of Magnetism and Photonics Group, Faculty of Mathematics and Natural Sciences, Bandung Institute of Technology, 10 Ganesha, Bandung 40132, Indonesia
Abstract:Spark ablation has been combined to microwave plasma torch atomic emission spectrometry for the direct analysis of compact metallic samples. The material is ablated by a medium voltage spark (450 V, 370 Hz) in a point-to-plane configuration and swept into a 100-W, 2.45-GHz argon microwave discharge. The microwave plasma is observed end-on and the radiation analysed with a polychromator. The detection limits for Fe, Ni, Pb and Sn in brass, Cr, Cu, Ni, Mn, Mo, Si and V in steel and Cu, Fe, Mg, Mn, Si and Zn in aluminium with the microwave plasma torch in the case of measurements with a polychromator are in the μg/g range and by a factor of up to 20 higher than those obtained with spark ablation coupled to inductively coupled plasma atomic emission spectrometry using a high resolution sequential spectrometer. The stability of the emission signal depends on the element studied and relative standard deviations usually are between 0.5 and 3.5%. In the case of low-alloy steels, the linearity and the precision of the calibration could be improved by internal standardisation. Several elements (Cr, Cu, Ni, Si and V) could be determined in a steel sample (BAS SS 410/1) with high accuracy and precision.
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