Elemental Analyses by ICP-AES



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Elemental Analyses by ICP-AES Henry Gong, Senior Analytical Chemist September 10, 2008

ICP-AES inductively coupled plasma atomic emission spectrophotometry Electrons of an atom absorb energy and jump to higher energy levels When they return to normal states, they emit characteristic photons of energy By isolating these photon wavelengths, we can determine the types and concentrations of the elements present. Concepts, Instrumentation, and Techniques in Inductively Coupled Plasma Optical Emission Spectrometry, Boss and Freeden, Perkin Elmer

Sample Introduction Solution is drawn up by means of a peristaltic pump Solution is turned into a fine aerosol by a nebulizer Aerosol is introduced into a plasma which excites the atomic species in the aerosol

Plasma Torch Ionized argon stream carrying current is roughly the surface temperature of the sun. Only a small portion of the plasma is sampled

Optical Path in an ICP-AES Materials Characterization Lab Prisms and echelle grating separate out (disperse) the wavelengths of emitted radiation into distinct, measurable, emission lines.

Elements by ICP-AES core electrons Different elements have different emission intensities. Alkalis (Na, K, Rb, Cs) are weakly emitting. Alkaline Earths (Be, Mg, Ca, Sr, Ba ) are strongly emitting.

Radial vs. Axial Viewing Radial traditional side view, better for concentrated samples. Axial direct view into plasma, lower sensitivity, shifts detection range lower.

Radial AND Axial Viewing Materials Characterization Lab

Common Problems in ICP-AES Sampling and Sample Preparation Spectral Interference Matrix Effects Instrumental Drift

Sampling and Sample Preparation Are the samples representative of what you are trying to measure? What steps should MCL take to make your samples representative? Will any elements volatilize during sample preparation? How much contamination can the sample tolerate during preparation?

Spectral Interference Some elemental lines may interfere with others. Best solution is to find another spectral line. Samples should be scanned for possible problems Concepts, Instrumentation, and Techniques in Inductively Coupled Plasma Optical Emission Spectrometry, Boss and Freeden, Perkin Elmer

Matrix Effects Differing viscosities can affect amount of sample uptake Matrices can change nature of plasma Certain matrices (HF) can attack torch Matrices can contain interfering spectral components

Combined Effects Concepts, Instrumentation, and Techniques in Inductively Coupled Plasma Optical Emission Spectrometry, Boss and Freeden, Perkin Elmer

Instrumental Drift Instrument reading can drift over a period of time due to physical changes in the optical system, or the configuration of the plasma. Standards need to be run at the beginning and end of each run in order to estimate and correct for this drift. Internal standards are used to compensate for differing matrices from sample to sample.

Compensation Standards run with every sample run Drift Correction or internal standardization is taken with every sample run Matrix of standards should be closely matched with that of the samples Preliminary scans are taken to see if any spectral overlaps occur

Basic Analytical Scheme Concepts, Instrumentation, and Techniques in Inductively Coupled Plasma Optical Emission Spectrometry, Boss and Freeden, Perkin Elmer

Sample Dissolution for Solid Samples Salt Fusions typically lithium metaborate and sodium peroxide Acid Digestions nitric, hydrochloric, perchloric and hydrofluoric Microwave Digestion basically acid digestion in controlled temperature and pressure vessels. Samples are typically dried, ashed if necessary, and ground to <74 microns prior to dissolution procedures

Salt Fusion Sample is mixed with lithium metaborate in a 1:9 ratio Mix is melted at 900C and dissolved in a nitric acid solution Pros: Attacks geologicals and most ceramics Provides a high concentration salt environment which dampens any intersample matrix differences. Cons: Easily volatilized elements cannot be determined High metal contents may prove difficult

Graphite crucible with lithium metaborate in furnace Materials Characterization Lab

Acid Digestion Sample is allowed to dissolve in an acid mix. Sample is typically heated to speed dissolution. Pros: Most direct dissolution, minimizing possible introduction of contaminants Usually best for metals Cons: Ineffective against geologicals and ceramics, especially if Si is to be determined Can be time consuming

Acid digestion in a Pt dish

Microwave Digestion Sample is allowed under controlled temperature and pressure conditions in a pressure vessel. Pros: Effective for a wide range of materials, especially those containing organics Direct method of dissolution, minimizing introduction of contaminants Cons: Time consuming method development Labor intensive

MARS 5 Microwave Digestion System

Data Reduction Concepts, Instrumentation, and Techniques in Inductively Coupled Plasma Optical Emission Spectrometry, Boss and Freeden, Perkin Elmer

What do the data mean? Precision and accuracy Precision is how well the instrument replicates data over time Accuracy is how close to the true value the observed results will be Precision is generally on the order of 2 to 5 relative weight percent Precision will vary from sample type to sample type depending on a number of factors

Typical Analytical Data Sample 1st 2nd 3rd Mean Extrapolated 04-1141 2.788 2.728 2.739 2.743 2.76 04-1152.279.269.268.272.27 04-1160 1.112 1.112 1.118 1.114 1.12 blank -.0005 -.0004 -.0003 -.0004 -.01

Typical applications of ICP-AES/ICP-MS Natural Waters Saline Brines Geological Materials Ceramics and glasses Coals and Paper Products Leachates

Natural Waters Leaching from mine sites Geochemical prospecting Sediment analyses

More Sample Types Discarded candy wrappers Glass and geologicals

Strengths of ICP-AES Can detect most cations and some anions Detection Limits down to parts per trillion for some elements Rapid simultaneous determination of selected elements Selective determination of other elements in sequential mode Good linear range up to hundreds of ppms for alkalis Suitable for routine analyses of multiple samples Dependable work horse type of instrument

Weaknesses of ICP-AES Not effective for low levels of alkalis (less than 1-5 ppm) subject to matrix problems suitable standards required on every run Only elemental data is provided - no direct structural information Does not provide, in most cases, parts per billion or parts per trillion data Go to ICP-MS

MCL capabilities: Perkin-Elmer Optima 5300 ICP-AES Lithium Metaborate and Sodium Peroxide Fusion capabilities. Acid Digestion Facilities MARS Microwave Digestion Capabilities

Acceptable sample forms: Solutions, preferably aqueous based with minimal or no HF Minimal solution volume is 3-4 ml or more depending on analyses Solids, can usually be dissolved using various techniques

Characterization Techniques for Solutions Concentration Level (ppm or mg/l) Technique >1 ICP-AES.01-1 ICP-AES, ICP-MS <.01 ICP-MS For unknown solutions, characterize with ICP-AES THEN use ICP- MS to determine lower concentrations of interest.

ICP-AES vs. ICP-MS ICP-AES is an atomic emission technique the inductively coupled plasma (ICP) serves as a means of exciting atoms and ions so that they emit characteristic wavelengths of energy. ICP-MS is a mass spectrometric technique the ICP serves only as a means of generating ions for the mass spectrometer.

ICP-AES ICP-MS Robust and cheap Dependable Student Proof (sort of) Good for routine analyses Delicate and expensive Finicky Student phobic Capable of extraordinary performances

Henry Gong 312 Hosler Bldg 865-1981 hxg3@psu.edu