scholarly journals Power Dissipation of an Inductively Coupled Plasma Torch under E Mode Dominated Regime

Micromachines ◽  
2021 ◽  
Vol 12 (7) ◽  
pp. 834
Author(s):  
Nan Yu ◽  
Renaud Jourdain ◽  
Mustapha Gourma ◽  
Fangda Xu ◽  
Adam Bennett ◽  
...  

This paper focuses on the power dissipation of a plasma torch used for an optical surface fabrication process. The process utilizes an inductively coupled plasma (ICP) torch that is equipped with a De-Laval nozzle for the delivery of a highly collimated plasma jet. The plasma torch makes use of a self-igniting coil and an intermediate co-axial tube made of alumina. The torch has a distinctive thermal and electrical response compared to regular ICP torches. In this study, the results of the power dissipation investigation reveal the true efficiency of the torch and discern its electrical response. By systematically measuring the coolant parameters (temperature change and flow rate), the power dissipation is extrapolated. The radio frequency power supply is set to 800 W, E mode, throughout the research presented in this study. The analytical results of power dissipation, derived from the experiments, show that 15.4% and 33.3% are dissipated by the nozzle and coil coolant channels, respectively. The experiments also enable the determination of the thermal time constant of the plasma torch for the entire range of RF power.

1987 ◽  
Vol 70 (4) ◽  
pp. 760-761
Author(s):  
Danton D. Nygaard ◽  
John J. Sotera

Abstract A modification of an inductively coupled plasma (ICP) emission spectrometer is described that enables the simultaneous determination of nitrogen, phosphorus, and potassium in water-soluble fertilizers. A quartz extension tube is added to the ICP torch to exclude air from the plasma, thus allowing accurate nitrogen determination without adversely affecting sensitivity for other analytes. The modification also requires an 18 mg/L argon coolant flow to protect the tube from the heat of the plasma. Detection limits are 20 mg/L for nitrogen and 50 μg/L for phosphorus and potassium. Three NBS reference salts and 2 commercially available fertilizers were analyzed by the method, and results are in excellent agreement with known values.


1983 ◽  
Vol 37 (4) ◽  
pp. 389-395 ◽  
Author(s):  
Ramon M. Barnes ◽  
Lancelot Fernando ◽  
Lu Shang Jing ◽  
Himansu S. Mahanti

Inductively coupled plasma-atomic emission spectroscopy (ICP-AES) is applied in the determination of 21 elements in primary, refined, and alloy aluminum. Rapid and reliable sample preparation procedures are developed. Spectral lines are selected after examination of experimental wavelength scans at each analyte wavelength. The limits of detection, background equivalent concentration, and analytical figures of merit are determined. For high silicon-containing aluminum, HF solutions were analyzed by employing an inert nebulizer utilizing polytetrafluoroethylene (PTFE) capillary tubes, a PTFE spray chamber, and an ICP torch with a graphite injector tube.


1987 ◽  
Vol 41 (4) ◽  
pp. 654-657 ◽  
Author(s):  
Thomas R. Smith ◽  
M. Bonner Denton

An inductively coupled plasma (ICP) torch utilizing an extended coolant tube that tapers down to a small exit orifice designed to increase the pressure within the ICP torch is described. This torch design makes use of the advantages associated with higher torch operating pressures (including improved detection limits, increased sensitivity, and better plasma stability), without requiring major modifications to existing commercially available ICP torch box and matching networks. Detection limits obtained with the use of the new torch design are compared with those obtained from several commonly used torch designs using a commercially available torch box and spectrometer. A two- to sevenfold improvement in detection limits is observed through increasing torch operating pressure from 101.325 KPa (760 Torr, or atmospheric pressure) to 120 KPa (900 Torr).


1987 ◽  
Vol 70 (4) ◽  
pp. 760-761
Author(s):  
Danton D Nygaard ◽  
John J Sotera

Abstract A modification of an inductively coupled plasma (ICP) emission spectrometer is described that enables the simultaneous determination of nitrogen, phosphorus, and potassium in water-soluble fertilizers. A quartz extension tube is added to the ICP torch to exclude air from the plasma, thus allowing accurate nitrogen determination without adversely affecting sensitivity for other analytes. The modification also requires an 18 mg/L argon coolant flow to protect the tube from the heat of the plasma. Detection limits are 20 mg/L for nitrogen and 50 μg/L for phosphorus and potassium. Three NBS reference salts and 2 commercially available fertilizers were analyzed by the method, and results are in excellent agreement with known values.


2020 ◽  
Vol 86 (10) ◽  
pp. 5-9
Author(s):  
D. G. Filatova ◽  
A. A. Arkhipenko ◽  
M. A. Statkus ◽  
V. V. Es’kina ◽  
V. B. Baranovskaya ◽  
...  

An approach to sorptive separation of Se (IV) from solutions on a novel S,N-containing sorbent with subsequent determination of the analyte in the sorbent phase by micro-x-ray fluorescence method is presented. The sorbent copolymethylenesulfide-N-alkyl-methylenamine (CMA) was synthesized using «snake in the cage» procedure and proven to be stable in acid solutions. Conditions for quantitative extraction of Se (IV) were determined: sorption in 5 M HCl or 0.05 M HNO3 solutions when heated to 60°C, phase contact time being 1 h. The residual selenium content in the solution was determined by inductively coupled plasma mass spectrometry (ICP-MS) using 82Se isotope. The absence of selenium losses is proved and the mechanism of sorption interaction under specified conditions is proposed. The method of micro-x-ray fluorescence analysis (micro-RFA) with mapping revealed a uniform distribution of selenium on the sorbent surface. The possibility of determining selenium in the sorbent phase by micro-RFA is shown. When comparing the obtained results with the results of calculations by the method of fundamental parameters, it is shown the necessity of using standard samples of sorbates to obtain correct results of RFA determination of selenium in the sorbent phase.


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