Atomic Emission Spectroscopy.IntroductionAtomic Emission SpectroscopyAdvantages of AAFlame Emission and Atomic Absorption Spectroscopy (3 main types)AES experiment set-upThree types of high-temperature plasmasThe Direct Current Plasma TechniquePicture of an inductively-coupled plasma atomic emission spectrometerA typical inductively coupled plasma source called a torchSlide 11AES WITH ELECTRICAL DISCHARGESELECTRODES FOR AESWAVELENGTH SELECTION AND DETECTION FOR AESQUALITATIVE ANALYSIS WITH ARC AND SPARK AESQUANTITATIVE ANALYSIS WITH ARC AND SPARK AES.ReferencesReferences (Cont’d.)Atomic Emission Spectroscopy.Chem. 331Introduction•Atomic absorption is the absorption of light by free atoms. An atomic absorption spectrophotometer is an instrument that uses this principle to analyze the concentration of metals in solution. The substances in a solution are suctioned into an excited phase where they undergo vaporization, and are broken down into small fragmented atoms by discharge, flame or plasma.Atomic Emission Spectroscopy•By exposing these atoms to such temperatures they are able to “jump” to high energy levels and in return, emit light. The versatility of atomic absorption an analytical technique (Instrumental technique) has led to the development of commercial instruments. In all, a total of 68 metals can be analyzed.Advantages of AA•Determination of 68 metals•Ability to make ppb determinations on major components of a sample•Precision of measurements by flame are better than 1% rsd. There are few other instrumental methods that offer this precision so easily.•AA analysis is subject to little interference.•Most interference that occurs have been well studied and documented.•Sample preparation is simple (often involving only dissolution in an acid)•Instrument easy to tune and operateFlame Emission and Atomic Absorption Spectroscopy (3 main types)•Atomic Emission (with thermal excitation), AES•Atomic Absorption, (with optical photon unit) AAS•Atomic Florescence, AFSAES experiment set-upThree types of high-temperature plasmas •The inductively coupled plasma (ICP).• The direct current plasma (DCP).•The microwave induced plasma (MIP). •The most important of these plasmas is the inductively coupled plasma (ICP).The Direct Current Plasma Technique •The direct current plasma is created by the electronic release of the two electrodes. The samples are placed on an electrode. In the technique solid samples are placed near the discharge to encourage the emission of the sample by the converted gas atoms.Picture of an inductively-coupled plasma atomic emission spectrometerA typical inductively coupled plasma source called a torchAtomic Emission Spectroscopy•Qualitative analysis is done using AES in the same manner in which it is done using FES. The spectrum of the analyte is obtained and compared with the atomic and ionic spectra of possible elements in the analyte. Generally an element is considered to be in the analyte if at least three intense lines can b matched with those from the spectrum of a known element.•Quantitative analysis with a plasma can be done using either an atomic or an ionic line. Ionic lines are chosen for most analyses because they are usually more intense at the temperatures of plasmas than are the atomic lines.AES WITH ELECTRICAL DISCHARGES •An electrical discharge between two electrodes can be used to atomize or ionize a sample and to excite the resulting atoms or ions. The sample can be contained in or coated on one or both of the electrodes or the electrode(s) can be made from the analyte. The second electrode which does not contain the analyte is the counter electrode.•Electrical discharges can be used to assay nearly all metals and metalloids. Approximately 72 elements can be determined using electrical discharges. For analyses of solutions and gases the use of plasmas is generally preferred although electrical discharge can be used. Solid samples are usually assayed with the aid of electrical discharges. •Typically it is possible to assay about 30 elements in a single sample in less than half an hour using electrical discharges. To record the spectrum of a sample normally requires less than a minute.ELECTRODES FOR AES •The electrodes that are used for the various forms of AES are usually constructed from graphite. Graphite is a good choice for an electrode material because it is conductive and does not spectrally interfere with the assay of most metals and metalloids. In special cases metallic electrodes (often copper) or electrodes that are fabricated from the analyte are used. •Regardless of the type of electrodes that are used, a portion of each of the electrodes is consumed during the electrical discharge. The electrode material should be chosen so as not to spectrally interference during the analysis.WAVELENGTH SELECTION AND DETECTION FOR AES •Arc and spark instruments normally contain non scanning monochromators. Either a series of slits is cut in the focal plane of the monochromator and a photomultiplier tube is placed behind each slit that corresponds to the wavelength of a line that is to be measured, or one or more photographic plates or pieces of film are placed on the focal of the monochromator.QUALITATIVE ANALYSIS WITH ARC AND SPARK AES •Qualitative analysis is performed by comparing the wavelengths of the intense lines from the sample with those for known elements. It is generally agreed that at least three intense lines of a sample must be matched within a known element in order to conclude that the sample contains the elementQUANTITATIVE ANALYSIS WITH ARC AND SPARK AES.•Regardless of the type of detection used for the assay, the precision of the results can be improved by matrix-matching the standards with the sample. Use of the internal-standard method also improves precision. Usually a working curve is prepared by plotting the ratio or logarithm of the ratio of intensity of the standard's line to the internal standard's line as a function of the logarithm of the concentration of the standard. The corresponding ratio for the analyte is obtained and the concentration determined from the working curve.References