Elimination of some spectral interferences and matrix effects in inductively coupled plasma-mass spectrometry using direct sample insertion techniques

Two key problem areas in inductively coupled plasma-mass spectrometry (ICP-MS) are spectral interferences from analyte and matrix based molecular ions, particularly oxide species; and non-spectroscopic matrix effects where an excess of an element, particularly heavier elements, suppresses the signal of lighter elements. It is shown that direct sample insertion (DSI) techniques can be used to eliminate some of these problems. With the absence of water in a DSI system, oxide species are reduced to a very low level ( .1%). Examples are shown for BaO⁺, CeO⁺ and ClO⁺. In addition, by relying on differential thermal volatilization, the suppressive matrix effect of U on Zn can be eliminated. Chemical modification with NaF is a key operational factor in achieving these benefits.     

Direct sample insertion for inductively coupled plasma spectrometry

Direct sample insertion (DSI) is an alternative sample introduction technique for inductively coupled plasma spectrometry whereby the sample, either liquid or solid, is placed onto or into a sample carrying probe which is inserted directly into the plasma. This review provides an overview of the DSI technique including instrumentation, operating parameters, system response, analytical figures of merit and applications.     

Background spectral characteristics in direct sample insertion-inductively coupled plasma-mass spectrometry

An extensive set of background spectra are presented for a direct sample insertion-inductively coupled plasma-mass spectrometer (DSI-ICP-MS) system. These include spectra of a dry plasma (i.e. one in which no sample or solvent is introduced) and background spectra for DSI sample probes such as graphite, Mo and Ta cups as well as a W wire loop. Compared to the background spectra measured when aqueous solutions are nebulized into the plasma the DSI background spectra are considerably simpler. Primarily due to the elimination of water in DSI systems there is a significant reduction and even elimination of numerous background species, particularly those containing oxygen and hydrogen. In addition, the DSI sample probes themselves do not add any complex species to the spectral background.     

An automated direct sample insertion system for the inductively coupled plasma

A new sample introduction system for inductively coupled plasma emission spectrometry is described. With this system, sample carrying cups can be sequentially and automatically inserted into an ICP discharge using a pneumatically activated transport system. The system carousel holds up to 24 cups (graphite or metal) and is located below a modified plasma torch that accommodates pneumatic injection of the entire sample carrying cup. The torch-insertion subassembly allows height programming of the final insertion and hence steps such as drying and ashing can be performed in situ. The system is applicable to the analysis of small volumes of liquids (10 μl) and small amounts (10 mg) of powders. The analytical characteristics will be presented including signal temporal behavior, detection limits and precision. Preliminary results indicate that the direct quantitative analysis of powdered botanicals and coal is feasible.     

Selenium speciation analysis using inductively coupled plasma-mass spectrometry

Selenium exists in several oxidation states and a variety of inorganic and organic compounds, and the chemistry of selenium is complex in both the environment and living systems. Selenium is an essential element at trace levels and toxic at greater levels. Interest in speciation analysis for selenium has grown rapidly in this last decade, especially in the use of chromatographic separation coupled with inductively coupled plasma-mass spectrometry (ICP-MS). Complete characterization of selenium compounds is necessary to understand selenium's significance in metabolic processes, clinical chemistry, biology, toxicology, nutrition and the environment. This review describes some of the essential background of selenium, and more importantly, some of the currently used separation methodologies, both chromatographic and electrophoretic, with emphasis on applications of selenium speciation analysis using ICP-MS detection.     

A new interface for combining capillary electrophoresis with inductively coupled plasma-mass spectrometry

This paper describes the development and design of a new, efficient, simple and robust interface for coupling capillary electrophoresis (CE) with inductively coupled plasma-mass spectrometry. The interface is based on a modified microconcentric nebulizer which permits a low flow rate of about 6 μL/min in the free aspiration mode. This interface construction provides an electrical connection for stable electrophoretic separations and adapts the flow rate of the electro-osmotic flow inside the CE capillary to the flow rate of the nebulizer for efficient transport of the analytes into the plasma. By optimization of the fluid mechanical properties the interface prevents the nebulizer from causing any laminar flow in the CE capillary and thus the high resolution power of CE can be preserved. Furthermore, this new device permits independent optimization of the nebulization from the CE whereby exact positioning of the CE capillary is not necessary, thus enabling fast exchange. A low dead volume spraychamber has been constructed which circumvents any band broadening of the sharp CE signals. Peak widths down to 3.5 s comparable to CE with UV detection are possible. Received: 5 February 1999 / Revised: 21 April 1999 / Accepted: 23 April 1999     

A new interface for combining capillary electrophoresis with inductively coupled plasma-mass spectrometry

This paper describes the development and design of a new, efficient, simple and robust interface for coupling capillary electrophoresis (CE) with inductively coupled plasma-mass spectrometry. The interface is based on a modified microconcentric nebulizer which permits a low flow rate of about 6 μL/min in the free aspiration mode. This interface construction provides an electrical connection for stable electrophoretic separations and adapts the flow rate of the electro-osmotic flow inside the CE capillary to the flow rate of the nebulizer for efficient transport of the analytes into the plasma. By optimization of the fluid mechanical properties the interface prevents the nebulizer from causing any laminar flow in the CE capillary and thus the high resolution power of CE can be preserved. Furthermore, this new device permits independent optimization of the nebulization from the CE whereby exact positioning of the CE capillary is not necessary, thus enabling fast exchange. A low dead volume spraychamber has been constructed which circumvents any band broadening of the sharp CE signals. Peak widths down to 3.5 s comparable to CE with UV detection are possible. Received: 5 February 1999 / Revised: 21 April 1999 / Accepted: 23 April 1999     

Effects of sampler-skimmer separation in inductively coupled plasma-mass spectrometry

The effects of varying the sampler-skimmer spacing in an inductively coupled plasma-mass spectrometer are illustrated. The signals for a number of species were monitored including background ions (ArN⁺, ArO⁺, ArOH⁺, Ar₂⁺, Ar₂H⁺), background continuum, analyte ions (Cu⁺, Ce⁺, La⁺), analyte oxide ions (CeO⁺, LaO⁺), and matrix induced ions (ArNa⁺). As the sampler-skimmer spacing is increased over that normally used, the signal for some species decreases in intensity while the signal for others increases in intensity. There is a wide range of differential behavior and in some cases the signal changes are quite dramatic.

In addition to presenting results for an Ar plasma, measurements are also presented for a N₂-Ar mixed gas plasma. For some species, the signal changes observed when the sampler-skimmer spacing is increased are quite different with the N₂-Ar mixed gas plasma than with the Ar plasma and are, in some cases, opposite to signal changes observed with the Ar plasma. It appears that a larger sampler-skimmer spacing is more appropriate for a N₂ mixed gas plasma than the spacing normally used for a pure Ar plasma. Finally the effect of sampler-skimmer spacing on matrix effects is presented and it appears that matrix effects are not induced in the zone between the sampler and the skimmer.     

A comparison of argon and mixed gas plasmas for inductively coupled plasma-mass spectrometry

The effects of adding N₂ to the outer gas flow of an Ar plasma in inductively coupled plasma mass spectrometry (ICP-MS) are illustrated. With 5% N₂ added to the outer gas flow and provided the central (nebulizer) gas flow is increased, modest signal enhancements (up to a factor of 4) are observed. The degree of enhancement depends on the extent to which an element forms a strong metal oxide bond and also, to some extent, on ionization potential. An important feature of N₂ mixed gas plasmas for ICP-MS is that the signals for analyte oxide species (MO⁺) and certain background species (ArO⁺, ArOH⁺, Ar₂⁺, ClO⁺, and ArCl⁺) are significantly reduced (an order of magnitude) by the addition of N₂ to the outer gas flow. In addition to these observations, some results are also presented for O₂ and air (outer gas) mixed gas plasmas and N₂ (central gas) mixed gas plasmas.     

Using inductively coupled plasma-mass spectrometry for calibration transfer between environmental CRMs

Multielement analyses of environmental reference materials have been performed using existing certified reference materials (CRMs) as calibration standards for inductively coupled plasma-mass spectrometry. The analyses have been performed using a high-performance methodology that results in comparison measurement uncertainties that are significantly less than the uncertainties of the certified values of the calibration CRM. Consequently, the determined values have uncertainties that are very nearly equivalent to the uncertainties of the calibration CRM. Several uses of this calibration transfer are proposed, including, re-certification measurements of replacement CRMs, establishing traceability of one CRM to another, and demonstrating the equivalence of two CRMs. RM 8704, a river sediment, was analyzed using SRM 2704, Buffalo River Sediment, as the calibration standard. SRM 1632c, Trace Elements in Bituminous Coal, which is a replacement for SRM 1632b, was analyzed using SRM 1632b as the standard. SRM 1635, Trace Elements in Subbituminous Coal, was also analyzed using SRM 1632b as the standard.     

An improved interface for inductively coupled plasma-mass spectrometry (ICP-MS)

Adiabatic sampling of the plasma from an inductively coupled plasma (ICP) torch is a crucial first step for inductively coupled plasma-mass spectrometry (ICP-MS) to reach its full potential as a trace multi-element analysis system. Previous results in the literature are reviewed, and a series of experiments reported, which indicate that a discharge, previously called a “pinch” effect, can be present in which the plasma properties are strongly altered by a constricted current flowing between the plasma and the sampling orifices, i.e. a secondary discharge. Measurements and calculations indicate that this mechanism is consistent with previously reported deleterious effects—abnormal production of doubly ionized species, a wide kinetic energy distribution for the ions sampled into vacuum, formation of ions from metal eroded from the sampling orifices, and a decreased orifice life-time. The mechanism producing the effect was found to be an unwanted capacitive coupling between the voltage on the induction coil and the plasma. Results are included which show that by centre-grounding the coil, the “pinch” effect can be reduced to negligible proportions. The resulting improvements for ICP-MS operation are described.     

Uranium colloid analysis by single particle inductively coupled plasma-mass spectrometry

Uranium single particle analysis has been performed by inductively coupled plasma-mass spectrometry (ICP-MS) and the performances are compared with that provided by scanning electron microsopy and single particle counting. The transient signal induced by the flash of ions due to the ionisation of an uranium colloidal particle in the plasma torch can be detected and measured for selected uranium ion masses (²³⁸U⁺, ²³⁵U⁺ or ²⁵⁴[²³⁸U¹⁶O]⁺) by the mass spectrometer. The signals recorded via time scanning are analysed as a function of particle size or fraction of the studied element or isotope in the colloid phase. The frequency of the flashes is directly proportional to the concentration of particles in the colloidal suspension. The feasibility tests were performed on uranium dioxide particles. The study also describes the experimental conditions and the choice of mass to detect uranium colloids in a single particle analysis mode.     

Automatic selection of internal standards in inductively coupled plasma-mass spectrometry

The automatic selection of internal standards in inductively coupled plasma-mass spectrometry was performed using a cluster analysis algorithm. The samples contained 25 analytes, spanning the atomic mass and ionization potential ranges, and a single interfering element. The interferents examined were Na, Mg, K, Zn, Ba, and Pb. The cluster analysis algorithm used kinetic energy, ionization potential, oxide bond strength, hydride bond strength, and electronegativity, to group the analytes. These variables were weighted differently in the various matrices. The performance of the clustering method and selection of internal standards was good for most analytes in the various matrices.     

On-line coupling of gel electrophoresis and inductively coupled plasma-mass spectrometry

The on-line coupling of gel electrophoresis with inductively coupled plasma-mass spectrometry (GE-ICP-MS) is a powerful tool for simultaneous separation, detection and quantification of bio-molecules, and has been applied to the determination of phosphorus in DNA, phosphoproteins, and phosphopeptides, gold in nano-particles, iron in metalloproteins, and iodine in aerosols, and cisplatin-oligonucleotide interactions. However, since the first report in 2005, relatively few papers have been published, perhaps reflecting the lack of familiarity with the benefits of this promising methodology. So, here for the first time, we critically review the applications of GE-ICP-MS, and explore the advantages and the limitations of the technique for various applications. Such scrutiny may be useful in not only the development of the technique but also highlighting its potential in proteomics, genomics and metallomics.     

Thorium colloid analysis by single particle inductively coupled plasma-mass spectrometry

Thorium colloid analysis in water has been carried out by a single particle mode using inductively coupled plasma mass spectrometry (ICP-MS). The flash of ions due to the ionisation of a thorium colloidal particle in the plasma torch can be detected and measured in a time scan for ²³²Th⁺ or ²⁴⁸[ThO]⁺ according to the sensitivity required by the mass spectrometer. The peaks of the recorded intensity of the MS signal can be analysed as a function of the particle size or fraction of the studied element in the colloid phase. The frequency of the flashes is directly proportional to the concentration of particles in the colloidal suspension. After discussing Th colloid detection, on the basis of the intensity of the ion flashes generated in the plasma torch, tests were performed on thorium dioxide colloidal particles. This feasibility study also describes the experimental conditions and the limitation of the plasma design to detect thorium colloids in a single particle analysis mode down to about 10 fg.     

电感耦合等离子体质谱法测定地球化学样品中镉

采用HF-HClO4-HNO3-H2SO4分解样品,王水提取,选用4个国家一级标准物质制备成标准系列校准,ICP-MS法直接测定地球化学样品中的Cd。选择103Rh为内标,确定了仪器的最佳分析条件,研究了Zr,Sn对Cd的干扰,选择114Cd作为测定同位素,采用数学公式校正了Sn对Cd的同质异位素干扰,方法检测限(3s)为6.3×10-3μg/g,RSD(n=12)为3.9%～6.6%。经国家一级标准物质验证,测定值与标准值吻合较好。该方法适用于地球化学样品中的微量Cd的测定。     

Employing multivariate calibration for the determination of radionuclides by inductively coupled plasma-mass spectrometry

A method for the simultaneous ICP-MS determination of α- and β-emitting radionuclides in acid digested samples of concrete without further sample pretreatment is presented. Spectral and non-spectral interferences are corrected for by combining systematic internal standardization with bilinear multivariate calibration. Consequently, especially for radionuclides with long half-lives, ICP-MS is an alternative to radiometric analytical methods. The optimal multivariate calibration approach is the PLS1-model with preselected variables.