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Inductively coupled plasma emission spectrometer

Selecting an approach A nearby lab specializes in mass spectrometric analysis and can perform the EPA screening method for pesticides and other toxic chemicals. Your own lab just bought an inductively coupled plasma emission spectrometer and can analyze the water for heavy metals. [Pg.832]

The current generation of inductively coupled plasma emission spectrometers provide limits of detection in the range of 0.1-500pg L 1 in solution, a substantial degree of freedom from interferences and a capability for simultaneous multi-element determination facilitated by a directly proportional response between the signal and the concentration of the analyte over a range of about five orders of magnitude. [Pg.39]

These workers used an ARC 34000 inductively coupled plasma emission spectrometer with flow-injection hydride generation. The 189.04nm line (3nd order) was used for arsenic measurement. The flow-injection block and Buckler peristaltic pump, as described by Liversage et al. [125] were also used for the determination of arsenic by hydride generation. [Pg.352]

Detailed operating conditions for the inductively coupled plasma emission spectrometer have been described by Brzezinska et al. [126]. [Pg.352]

An inductively coupled plasma emission spectrometer does not require any lamps and can measure as many as —70 elements simultaneously. Color Plates 23 and 24 illustrate two designs for multielement analysis. In Plate 23, atomic emission enters the polychromator and... [Pg.463]

Procedure Set up an inductively coupled plasma emission spectrometer according to manufacturer s instmctions, using the lead emission line at 220.35 nm. Calibrate the instmment using the Standard Lead Blank Solution and the Diluted Standard Lead Solution. Then analyze the Sample Preparation and the Control Lead Solution. The sample passes the test if the lead concentration found in the Sample Preparation is equal to or less than that in the Control Lead Solution. [Pg.323]

Any type of detector with a flow-through cell can be used for FIA. Photometric detectors are most often used in FIA (15-18, 25). However, many other analyses using fluorimeters (28, 29), refractometers (24), atomic absorption (30, 31), and inductively coupled plasma emission spectrometers (32) have been described. Electrochemical detectors based on potentiometry with ion-selective electrodes (15, 33), anodic stripping voltammetry (15, 34), potentiometric stripping (35), and amperometry (36) have also been used. [Pg.14]

Direct-current and inductively coupled plasma emission spectrometers... [Pg.41]

Beryllium Acetyl-acetone in chioroform Inductively coupled plasma emission spectrometer lOpgper 30ml [765]... [Pg.400]

Much more sensitive and less time-consuming techniques such as mass spectrometry, atomic emission, and atomic absorption are needed for the analysis of pollutants. Detectors such as graphite furnace-atomic absorption spectrometer (GF-AAS), inductively coupled plasma-mass spectrometer (ICP-MS), or inductively coupled plasma-atomic emission spectrometer (ICP-AES) seem to be ideal candidates for the analysis of trace metals because of their very low detection limits. The high temperatures used avoid the need for tedious digestions in many samples. FFF-gas chromatography-mass spectrometry could perhaps be used in the analysis of particular organic molecules. [Pg.1210]

The increased reproducibility of spark emission is more conducive to quantitative analysis than is arc emission. Spark emission spectrometers often employ a more sophisticated detection system. Rather than impinging on a photographic plate, the dispersed radiation passes onto an array of photomultiplier tubes positioned at preset wavelengths. The photomultiplier is more accurate and faster to use in quantitative measurements than film (12). Such an instrument is called a direct reader and will be discussed further in relation to inductively coupled plasma emission spectroscopy. [Pg.422]

The gas chromatograph may be interfaced with atomic spectroscopic instruments for specific element detection. This powerful combination is useful for speci-ation of different forms of toxic elements in the environment. For example, a helium microwave induced plasma atomic emission detector (AED) has been used to detect volatile methyl and ethyl derivatives of mercury in fish, separated by GC. Also, gas chromatographs are interfaced to inductively coupled plasma-mass spectrometers (ICP-MS) in which atomic isotopic species from the plasma are introduced into a mass spectrometer (see Section 20.10 for a description of mass spectrometry), for very sensitive simultaneous detection of species of several elements. [Pg.587]

Generally the alkali metals (Li, Na, K, Rb, Cs), the alkali earth metals (Mg, Ca, Sr, Ba) and other metals (e.g. Fe, Mn, Si, Al, Cu, Zn, Cr, Co, Ni) are determined in the acid-preserved pore water samples. Analytical details depend on the special conditions provided by the applied analytical instruments ICP-AES (Inductively Coupled Plasma Atomic Emission S.pectrometer), ICP-MS (Inductively Coupled Plasma Mass Spectrometer), or AAS (Atomic Absorption Spectrometer) of the respective laboratory. A discussion of details is not appropriate in this chapter. In most cases dilutions of 1 10 or 1 100 will be measured depending on the salt content in marine environments, so that the required sample amounts are rather low. [Pg.104]

Part III provides several conventional, environmental evaluation processes for surface finishing. In chapter The Necessity and Meaning , we describe the necessity and meaning of enviromnental evaluation for surface finishing. Also we discuss evaluation processes that have already been used. In chapter Frequently Used Evaluations for Effluents , the Inductively Coupled Plasma Atomic Emission Spectrometer (ICP-AES) and the Inductively Coupled Plasma Mass Spectrometer (ICP-MS) are mainly described and discussed as conventional, but powerful analytical tools. In chapter Frequently Used Evaluations for Aerial and Solid Pollution , the conventional analyses for aerial and solid pollution are presented. These types of pollution have caused very serious problems. Therefore, various countermeasures have been devised for them. And even nowadays, new problems such as air pollutants called particulate matter are emerging. These air pollutants include solid particles and liquid droplets that come in various sizes. The small particles that are 2.5 pm or less are called PM2.5. In this chapter, we also focus oti gas chromatography/ion chromatography from the fundamental viewpoint. In chapter Dissolution Assay , the dissolution assay process is described. This type of analysis is used to measure the dissolution amounts and characteristics for many kinds of metal components of materials. [Pg.9]

A novel technique of atomisation, known as vapour generation via generation of the metal hydride, has been evolved, which has increased the sensitivity and specificity enormously for these elements [5-7]. In these methods the hydride generator is linked to an AAS (flame graphite furnace) or inductively coupled plasma-optical emission spectrometer (ICP-OES) or an inductively coupled plasma mass spectrometer (IPC-MS). Typical detection limits achievable by these techniques range from 3 pg/1 (arsenic) to 0.09 pg/1 (selenium). [Pg.345]

Prohaska,T., Pfeffer, M.,Tulipan, M., Stingeder, G., Mender, A., and Wenzel, WW. (1999). Speciation of arsenic of liquid and gaseous emissions from soil in a microcosmos experiment by liquid and gas chromatography with inductively coupled plasma mass spectrometer (ICP-MS) detection. Fresenius J.Anal. Chem. 364(5), 467. [Pg.257]

Concentrations of total arsenic in soil and water samples contaminated with old Arsenical Munitions are not very useful to characterize the potential risks. Knowledge of which arsenic compounds are present in such samples is absolutely necessary to define toxicity. The identification of arsenic compounds requires a separation step combined with a detection step. For separation, gas chromatography and high performance liquid chromatography are widely used. Atomic absorption spectrometers, inductively coupled plasma optical emission spectrometers, and inductively coupled plasma mass spectrometers may serve as arsenic-specific detectors. [Pg.151]


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See also in sourсe #XX -- [ Pg.36 , Pg.41 , Pg.42 ]




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