Evaluation, Control and Diagnosis of an ICP Through Simple Experiments

Similar documents
Analysis Repeatability of Trace and Major Elements in a Water Sample

Optimizing Analytical Performance in ICP-OES Applications

PRINCIPLE OF ICP- AES

Chapter 9. Atomic emission and Atomic Fluorescence Spectrometry Emission spectrophotometric Techniques

Fast Analysis of Water Samples Comparing Axially-and Radially- Viewed CCD Simultaneous ICP-OES

Atomic Emission Spectroscopy

DETERMINATIONS OF THE POLLUTION LEVEL OF THE ENVIRONMENT WITH HEAVY METALS

Ultra-fast determination of base metals in geochemical samples using the 5100 SVDV ICP-OES

a. An emission line as close as possible to the analyte resonance line

OES - Optical Emission Spectrometer 2000

Pulsed RF Glow Discharge Optical Emission Spectrometry. Ultra Fast Elemental Depth Profiling GD-OES

Analysis of domestic sludge using the Agilent 4200 MP-AES

Elemental analysis of river sediment using the Agilent 4200 MP-AES

ICP-3000 Inductively Coupled Plasma Optical Emission Spectrometer

Direct Analysis of Photoresist Using Inductively Coupled Plasma Mass Spectrometry (ICP-MS) Application

Rapid and precise calcium isotope ratio determinations using the Apex-ACM desolvating inlet system with sector-field ICP-MS in low resolution

U.S. EPA SW-846 Method 6010C using the Prodigy High Dispersion ICP

Direct Analysis of Trace Metal Impurities in High Purity Nitric Acid Using ICP-QQQ

Hydride Generation for the Determination of As, Sb, Se and Bi Using the Teledyne Leeman Lab s Prodigy 7 ICP-OES

ELEMENT2 High Resolution- ICP-MS INSTRUMENT OVERVIEW

INDUCTIVELY COUPLED PLASMA MASS SPECTROMETRY

Direct Measurement of Metallic Impurities in 20% Ammonium Hydroxide by 7700s/7900 ICP-MS

Atomic Absorption & Atomic Fluorescence Spectrometry

Quantitative analysis of high purity metals using laser ablation coupled to an Agilent 7900 ICP-MS

Atomic Spectroscopy AA/ICP/ICPMS:

Techniques for the Analysis of Organic Chemicals by Inductively Coupled Plasma Mass Spectrometry (ICP-MS)

- A spark is passed through the Argon in the presence of the RF field of the coil to initiate the plasma

Multi-Element Analysis of Petroleum Crude Oils using an Agilent 7900 ICP-MS

Pulsed RF Glow Discharge Optical Emission Spectrometry. Ultra Fast Elemental Depth Profiling GD-OES

Spectrometric Methods of Analysis. OCN 633 Fall 2013

Meeting the Challenges of Soil Analysis with the Avio 200 ICP-OES

Analysis of high matrix samples using argon gas dilution with the Thermo Scientific icap RQ ICP-MS

Determination of major, minor and trace elements in rice fl our using the 4200 Microwave Plasma- Atomic Emission Spectrometer (MP-AES) Authors

Performance Evaluation of an Axially Viewed Horizontal Inductively-Coupled Plasma for Optical-Emission Spectrometry

Environmental Series - Trace contaminant analysis in brine using a Thermo Scientific icap 6000 Series Duo ICP

9/13/10. Each spectral line is characteristic of an individual energy transition

Total Elemental Analysis of Food Samples for Routine and Research Laboratories, using the Thermo Scientific icap RQ ICP-MS

Determination of Total Bromine and Iodine Emission Spectrometric Method (ICP-OES) EuSalt/AS

Inductively Coupled Plasma Mass Spectrometry (ICP-MS) Debjani Banerjee Department of Chemical Engineering IIT Kanpur

Low level Os isotopic measurements using multiple ion counting

Use of ICP-MS in analysing radioisotopes. Per Roos Risø National Laboratory for Sustainable Energy, Technicial University of Denmark

Application. Determination of Trace Metal Impurities in Semiconductor-Grade Hydrofluoric Acid. Authors. Introduction. Abstract.

Determination of Impurities in Silica Wafers with the NexION 300S/350S ICP-MS

AN INTRODUCTION TO ATOMIC SPECTROSCOPY

10/2/2008. hc λ. νλ =c. proportional to frequency. Energy is inversely proportional to wavelength And is directly proportional to wavenumber

Unité d Agronomie, Centre de recherches INRA de Bordeaux, B.P. 81, Villenave d Ornon Cedex, France

Atomization. In Flame Emission

Emission spectrum of H

high temp ( K) Chapter 20: Atomic Spectroscopy

Low-field helicon discharges

ICP-OES Application Note Number 35

U.S. EPA SW-846 Method 6010C Using the Prodigy7 High- Dispersion ICP Introduction. Application Note - AN1305. Experimental

Lecture 7: Atomic Spectroscopy

CHAPTER 4: ANALYTICAL INSTRUMENTATION

Report of the Inter-laboratory Comparison Project 2004 on Wet Deposition

Determination of trace elements in ultrapure semiconductor grade sulfuric acid using the Agilent 8900 ICP-QQQ in MS/MS mode

Trace elemental analysis of distilled alcoholic beverages using the Agilent 7700x ICP-MS with octopole collision/ reaction cell

Determination of ultratrace elements in photoresist solvents using the Thermo Scientific icap TQs ICP-MS

Optical Atomic Spectroscopy

SmartNotes. What is meant by the term interference?

Estapor Microspheres n 11. A technical newsletter published by Merck Chimie SAS - France

USGS Troy WSC Laboratory Inductively Coupled Plasma- NH4Cl Soil Extracts SOP 425 Jordan Road Rev. No. 2.0 Troy, NY Date: 03/16/2012 Page 1 of 7

Ultra trace measurement of potassium and other elements in ultrapure water using the Agilent 8800 ICP-QQQ in cool plasma reaction cell mode

Enhancing the productivity of food sample analysis with the Agilent 7700x ICP-MS

Application note. Determination of exchangeable cations in soil extracts using the Agilent 4100 Microwave Plasma-Atomic Emission Spectrometer

Overcoming Interferences with the Thermo Scientific icap 7000 Plus Series ICP-OES

CHEM*3440. Photon Energy Units. Spectrum of Electromagnetic Radiation. Chemical Instrumentation. Spectroscopic Experimental Concept.

ENVG FALL ICP-MS (Inductively Coupled Plasma Mass Spectrometry) Analytical Techniques

Chemistry 524--Final Exam--Keiderling May 4, :30 -?? pm SES

Application note. Trace level analysis of sulfur, phosphorus, silicon and chlorine in NMP using the Agilent 8800 Triple Quadrupole ICP-MS

Observation of Self Absorption of Mercury I and Cadmium I Emission in an Atmospheric Microwave Sustained Plasma

All about sparks in EDM

Carbon, sulfur and phosphorus-based charge transfer reactions in inductively coupled plasma atomic emission spectrometry

Determination of the Halogen Elements in the Deep UV Region of the Spectrum by ICP - OES

2101 Atomic Spectroscopy

INTRODUCTION TO OPTICAL ATOMIC SPECTROSCOPY (Chapter 8)

The Evolution of Inductively Coupled Plasma - Optical Emission Spectroscopy (ICP-OES)

3 - Atomic Absorption Spectroscopy

Course Details. Analytical Techniques Based on Optical Spectroscopy. Course Details. Textbook. SCCH 211: Analytical Chemistry I

Because light behaves like a wave, we can describe it in one of two ways by its wavelength or by its frequency.

Supporting Information

atomic absorption spectroscopy general can be portable and used in-situ preserves sample simpler and less expensive

CHAPTER 8. SUMMARY AND OUTLOOK 90 Under the operational conditions used in the present work the translation temperatures can be obtained from the Dopp

Trace Analyses in Metal Matrices Using the ELAN DRC II

Simplified Analysis for Soil Samples with Compact Water Quality Meter <LAQUAtwin>

Ch. 8 Introduction to Optical Atomic Spectroscopy

NATIONAL ASSOCIATION OF TESTING AUTHORITIES (NATA) REQUIREMENTS FOR ACCREDITATION OF ICP-MS TECHNIQUES

DEPARTMENT OF CHEMISTRY UNIVERSITY OF SWAZILAND

Accurate Analysis of Trace Mercury in Cosmetics using the Agilent 8900 ICP-QQQ

Sources of Errors in Trace Element and Speciation Analysis

A Multi-beamlet Injector for Heavy Ion Fusion: Experiments and Modeling

Chemistry Department Faculty Publication Series

NATURE AN POLUUTION DEGREE OF WATER ASSETS STUDIED BY INDUCTIVELY COUPLED PLASMA-OPTICAL EMISSION SPECTROSCOPY

Following documents shall be used for reference on quantities, units, prefixes and other technical vocabulary in this document:

Cesium Dynamics and H - Density in the Extended Boundary Layer of Negative Hydrogen Ion Sources for Fusion

Two-dimensional Fluid Simulation of an RF Capacitively Coupled Ar/H 2 Discharge

Chapter 8: An Introduction to Optical Atomic Spectrometry

Liberty Series II. Liberty. Liberty Series II. Analytical Methods book. Publication No October (i) Publication date: 10/99

High-Speed Environmental Analysis Using the Agilent 7500cx with Integrated Sample Introduction System Discrete Sampling (ISIS DS)

Interface (backside) & Extraction Lens

Transcription:

ICP OPTICAL ATOMIC EMISSION SPECTROSCOPY Evaluation, Control and Diagnosis of an ICP Through Simple Experiments Odile Hirsch HORUIBA Scientific, Longjumeau, France Keywords: general 1 Introduction To undertake an analysis, one must go through a long chain of processes from sampling to reporting of the results. To obtain reliable results, the chemist must ensure that none of these steps introduces a systematic error. To do this, checks must be made on each process. In the case of ICP, it is necessary to check, by means of a set of tests, that the instrument provides the initial analytical performance used as a comparison basis. The set of tests provide: 1) Checks on the main components of the ICP, 2) Diagnosis of any malfunctions, 3) Checks on analytical performance. More particularly, the following parameters are checked: repeatability and reproducibility, accuracy, absence of drift (long term stability), selectivity (practical resolution of the dispersion system), absence of matrix effects or inter-element effects and detection limits. Highly sophisticated diagnostic tests have been developed and described in the literature for understanding the role of the plasma and the effects of the operating parameters. The understanding of ICPs have been considerably improved by these experiments, but it is difficult to implement them on commercially available ICP systems. It is therefore necessary to provide simple experiments that can be applied more widely. This motivated the development of a set of tests based on previous work on drift [1], on the measurement of the practical resolution [2], on diagnosis using the ratio of the intensity of an ionic to that of an atomic line [3], and on a scale of detection limits [4]. If you would like more information on this subject, you can read the publication Simple experiments for the control, the evaluation and the diagnosis of inductively coupled plasma sequential systems, E. Poussel, J.M. Mermet, O. Samuel-Hirsch, Spectrochimica Acta, 48B, 743-755 (1993) and also you can obtain document A0037/1/E from HORIBA Scientifc. 2 Effect of ICP components on analytical performance An ICP consists of the following main components: an RF generator, an inductor to generate the plasma, a torch to confine the discharge, a sample injection system (nebulizer, spray chamber and injector), a collimator, a dispersion system and a detector. Each component can have an effect on the analytical characteristics (Table 1). Table 1: Effect of component on analytical characteristics Generator Optics Nebulization Detection Repeatability * * * * Accuracy * Stability * * * Interferences * * Selectivity * Limits of detection * * * * Repeatability can be degraded by lack of stability of the RF generator matching unit; by fluctuations in the transport of the aerosol or the drain, insufficient integration time favoring shot noise, or by the photomultiplier tube noise caused by inadequate bandwidth of the dispersion system. Reproducibility can be affected by the replacement of one of the components, in particular replacement of the torch. A lack of long-term stability, indicated by drift, may be caused by a change in the applied power, or in the gas flow rates. Other causes include partial clogging of the nebulizer, a change in the temperature of the spray chamber and a deposit on the injector tube. The dispersion system may also contribute to drift by contamination of the collimation system (lens or mirror, possibly optical fibers) and a change in the focusing and wavelength positioning conditions.

ICP OPTICAL ATOMIC EMISSION SPECTROSCOPY It has been shown that matrix effects are minimized by using a high generator power (>1.2 kw) and a long sample dwell time. The latter is obtained by using aerosol gas flowrates below 1 L/min. It is therefore important to check the power and the gas flow rates. Good selectivity is essentially related to the practical resolution of the dispersion system, which can be degraded by a change in the position of an optical component (for example caused by vibrations). Good detection limits can be obtained only if each constituent part of the ICP system is operating under ideal conditions. The detection limit is known to depend on the relative standard deviation of the fluctuations in the background and on the signal-to-background ratio as well as the optics. The latter is related to the effectiveness of the nebulizer and to the bandwidth of the system. The relative standard deviation depends on the shot noise (minimized by longer integration time and smaller bandwidth) and on the flicker noise (RF generator and sample injection system). The detection limits must therefore be checked after ensuring that each part satisfies specified criteria. 3 Elements and tests In addition to naturally available argon, a limited number of elements are used in the set of tests: Ba (5 mg/l), Mg (5 mg/l) and Zn (5 mg/l). The lines used and the energies are given in Table 2 Table 2: Excitation Energy (E exc ), Ionization Energy (E ion ), and the sum of these two energies (E sum ) for different lines used in this diagnosis Elements E exc (ev) E ion (ev) E sum (ev) Ar I 404 nm 14.69 14.69 Ba II 455 nm 2.72 5.21 7.93 Ba II 233 nm 6.01 5.21 11.22 Mg I 285 nm 4.35 4.35 Mg II 280 nm 4.42 7.65 12.07 Zn II 206 nm 6.01 9.39 15.40 Although the number of lines in Table 2 is limited, a large amount of information can be obtained, by considering the line width, the absolute intensity, the ratio of the intensities of a pair of ionic and atomic lines, and the relative standard deviation of the intensity. The use made of the lines is summarized in Table 3. Table 3: Use of the test elements for the evaluation and the diagnosis of the ICP system Line and Test Measurement Component Ba II 233 nm: profile UV resolution Dispersive system Ba II 455 nm: profile Vis resolution Dispersive system Mg II 280/ Mg I 285 Energy transfer Generator Background 455/Background 233 nm Lens/mirror contamination Collimator Mg I 285 nm/ adjacent background Nebulizer effectiveness Nebulizer RSD Mg I 285 nm Nebulizer repeatability Nebulizer RSD Mg I 285 nm Reproducibility ICP system Ba II 233 nm Detection limit ICP system Zn II 206 nm Detection limit ICP system RSD Ar I 404 nm Drift ICP system RSD Zn II 206 nm Drift ICP system RSD Ba II 455 nm Drift ICP system 2

4 Flow chart of the procedure The experiment described in the previous section must be performed according to a given sequence (shown in Figure 1). The first step is to verify the practical resolution of the optical system, as this measurement is independent of the RF generator efficiency and the sample introduction system. The second step is to verify that the transfer of energy is adequate by using the line intensity ratio of Mg II to Mg I. If this ratio is good, one can compare the 455/233 signal intensity ratio, and if the value is higher, this could signify that there is absorption of light. The following step is to check the nebulizer by measuring the SBR of the Mg I 285 line. If the excitation conditions are constant as previously checked, the SBR of the Mg I line depends mainly on the efficiency of the nebulizer. Subsequently, the stability of the sample introduction system is assessed through the value of the RSD. Finally, the limits of detection of Ba II 455 nm and Zn II 206 nm are measured and compared to previous values. A drift test can be carried out by the use of the Ba II 455 nm and Zn II 206 nm lines. 3 Figure 1: Flow chart of the procedure used for the evaluation and the diagnosis of an ICP system

5 Example of long term diagnosis Results shown in Table 4 represent data from a JY 24/124 instrument. This instrument is used for a variety of matrices, including cement, bitumen, and wastewater. This leads to numerous changes of the sample introduction system. One can see that the RSD over 6 months are very good, except for the sample introduction system, because nebulizer clogging occurred causing the nebulizer to be changed twice. Table 4: Example 1 Duration Mean value Sigma RSD(%) Energy transfer 6 months 10.5 0.37 3.5 Optics transfer 6 months 9.3 0.4 4.3 Nebulizer efficiency 2.5 months 124 6.4 5.2 Repeatability 6 months 0.8 Reproducibility 2.5 months 2308 182 7.9 Zn Limit of detection 2.5 months 1.2 0.55 Table 5 represnt data from a JY38/138/238/ULTIMA instrument. The matrices analyzed on this instrument are various types of wastewater and oil. The results show very good performance over more than one year. Table 5: Example 2 Duration Mean value Sigma RSD(%) Energy transfer 13 months 9.3 0.68 7.3 Optics transfer 13 months 0.98 0.26 Nebulizer efficiency 4 months 487 11.7 2.4 Repeatability 13 months 0.5 % Reproducibility 4 months 1108 58 5.2 4

5 Figure 2: Resolution, energy transfer, light absorption, and efficiency curves

6 Example of a malfunction in the instrument This example illustrates the detection of a degradation in the energy transfer of the JY138 ICP system based on the use of the Mg II/Mg I line intensity ratio. The ratio is shown over a period of two months. During the first month of the experiment, a decrease in the ratio was observed which clearly indicated a change in either the power or the energy transfer. In fact, the system had a blockage in the recirculating water cooling system of the load coil. The system was cleaned with acidified water, then with deionized water. Unfortunately, some acidified water remained in the circuit causing the dissolution of copper from the coil. Because of the increase in the conductivity of water, some power was therefore dissipated into the water instead of being transferred into plasma. Once the origin of this problem was found, the circuit was carefully cleaned, resulting in a two-fold improvement in the intensity ratio. Then, over a period of more than one month, regular checks indicated no significant change in the ratio. Mg Ratio Corrosion of the coil Figure 3: Example of malfunction 6

ICP OPTICAL ATOMIC EMISSION SPECTROSCOPY 7 Conclusion Previously sophisticated diagnostics could only be carried out in research laboratories. Now, however, it is possible to perform some simple experiments in order to control and evaluate an ICP system and to identify problems. Among these tests, the one using the ratio of the Mg lines is the most critical, as many parameters can affect it. The experiments described are fast and easy to conduct and can be stored as a standard analytical method and can provide some explanation about the origin of a degradation of the analytical performance. To obtain a ratio that remains constant to within a few percent over a period of several weeks or months requires rigorous maintenance of the instrument (replacement of a component, adjustment of operating parameters) but this will provide high reproducibility of analytical performance. 8 References [1] M Carré, E. Poussel and J.M.Mermet, J.Anal.Atom.Spectrom. 7, 791 (1992) [2] J.M. Mermet, J.Anal.Atom.Spectrom. 2, 681 (1987) [3] J.M.Mermet, Anal.Chim.Acta 250, 85 (1991) [4] M.Marichy, M.Mermet, M.Murillo, E.Poussel and J.M.Mermet, J.Anal.Atom.Spectrom. 4, 209 (1989) These experiments can also be easily adapted to set up control charts, once the accepted values of the line intensities and ratios and their fluctuations have been determined. info-sci.fr@horiba.com www.horiba.com/scientific France: HORIBA Jobin Yvon S.A.S., 16-18 rue du Canal, 91165 Longjumeau Cedex - Tel: +33 (0)1 64 54 13 00 - Fax: +33 (0)1 69 09 07 21 - Email: info-sci.fr@horiba.com USA: HORIBA Jobin Yvon Inc., 3880 Park Avenue, Edison, NJ 08820-3012. Toll-free: +1-866-jobinyvon - Tel: +1-732-494-8660 - Fax: +1-732-549-5125 Email: info-sci.us@horiba.com Japan: HORIBA Ltd., Scientific Instruments Sales Dept., Alte-Building Higashi-Kanda, 1-7-8 Higashi-Kanda, Chiyoda-ku, 101-0031 Tokyo - Tel: +81 (0)3 3861 8231 Fax: +81 (0)3 3861 8259 - Email: info-sci.jp@horiba.com Germany: HORIBA Jobin Yvon GmbH, Hauptstrasse 1, 82008 Unterhaching - Tel: +49 (0)89 46 23 17-0 - Fax: +49 (0)89 46 23 17-99 - Email: info-sci.de@horiba.com Italy: HORIBA Jobin Yvon Srl, Via Cesare Pavese 35/AB, 20090 Opera (Milano) - Tel: +39 0 2 57 60 30 50 - Fax: +39 0 2 57 60 08 76 - Email: info-sci.it@horiba.com UK: HORIBA Jobin Yvon Ltd, 2 Dalston Gardens, Stanmore, Middlesex HA7 1BQ - Tel: +44 (0)20 8204 8142 - Fax: +44 (0)20 8204 6142 - Email: info-sci.uk@horiba.com China: HORIBA Jobin Yvon SAS, Room 1801, Capital Tower No.6, Jianguomenwai Av., Chaoyang District, Beijing 100022 - Tel: +86 (0)10 8567 9966 - Fax: +86 (0)10 8567 9066 Email: info-sci.cn@horiba.com Other Countries: Tel: +33 (0)1 64 54 13 00 - Email: info.sci@horiba.com 7