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Chromatographic analysis, requirements

A key to elemental analysis is dynamic flash combustion, which creates a short burst of gaseous products, instead of slowly bleeding products out over several minutes. This feature is important because chromatographic analysis requires that the whole sample be injected at once. Otherwise, the injection zone is so broad that the products cannot be separated. [Pg.638]

Gas chromatographic analysis requires that a compound exhibit at least a few mm of vapor pressure at the highest temperature at which it is stable. In many cases, organic compounds that cannot be passed through a chromatographic column directly can be converted to derivatives that are amenable to gas chromatographic analysis. It is seldom possible to analyze organic compounds in water by direct... [Pg.789]

This type of analysis requires several chromatographic columns and detectors. Hydrocarbons are measured with the aid of a flame ionization detector FID, while the other gases are analyzed using a katharometer. A large number of combinations of columns is possible considering the commutations between columns and, potentially, backflushing of the carrier gas. As an example, the hydrocarbons can be separated by a column packed with silicone or alumina while O2, N2 and CO will require a molecular sieve column. H2S is a special case because this gas is fixed irreversibly on a number of chromatographic supports. Its separation can be achieved on certain kinds of supports such as Porapak which are styrene-divinylbenzene copolymers. This type of phase is also used to analyze CO2 and water. [Pg.71]

Polyacrylates are an industrially important class of polymers. The name polyacrylate is variously used to refer to polymers of acrylate esters [e.g., poly(methyl methacrylate)] as well as polymers of acrylic acids [e.g., poly(meth-acrylic acid)]. Because the former is organic soluble while the latter is not, chromatographic analysis of these two requires quite different conditions. This chapter discusses both types of polymers, separating their consideration when necessary. We will refer to both types of polymers as polyacrylates, letting the context indicate whether we are referring to an ester or to an acid polymer. [Pg.539]

A reliable chromatographic method has been developed for the quantitative aneilysis of hydrophobic impurities in water-soluble polymeric dyes. The method utilizes both the molecular sieve effect of normal gel permeation chromatography and solute-column packing interaction, modified by solvent composition. This method eliminates the need to extract the impurities from the polymeric dye with 100 extraction efficiency, as would be required for an ordinary liquid chromatographic analysis. [Pg.301]

Trace analysis of soil samples often requires post-extraction cleanup to remove coextracted matrix interferences. There are several difficulties that may arise during chromatographic analysis due to interferences present in sample extracts. To avoid these and other issues, one or more of the following cleanup techniques are often used. [Pg.876]

HS-GC methods have equally been used for chromatographic analysis of residual volatile substances in PS [219]. In particular, various methods have been described for the determination of styrene monomer in PS by solution headspace analysis [204,220]. Residual styrene monomer in PS granules can be determined in about 100 min in DMF solution using n-butylbenzene as an internal standard for this monomer solid headspace sampling is considerably less suitable as over 20 h are required to reach equilibrium [204]. Shanks [221] has determined residual styrene and butadiene in polymers with an analytical sensitivity of 0.05 to 5 ppm by SHS analysis of polymer solutions. The method development for determination of residual styrene monomer in PS samples and of residual solvent (toluene) in a printed laminated plastic film by HS-GC was illustrated [207], Less volatile monomers such as styrene (b.p. 145 °C) and 2-ethylhexyl acrylate (b.p. 214 °C) may not be determined using headspace techniques with the same sensitivities realised for more volatile monomers. Steichen [216] has reported a 600-fold increase in headspace sensitivity for the analysis of residual 2-ethylhexyl acrylate by adding water to the solution in dimethylacetamide. [Pg.205]

Another method to detect energy transfer directly is to measure the concentration or amount of acceptor that has undergone an excited state reaction by means other than detecting its fluorescence. For instance, by chemical analysis or chromatographic analysis of the product of a reaction involving excited A [117, 118]. An early application of this determined the photolyzed A molecules by absorption spectroscopic analysis. [119-121], This can be a powerful method, because it does not depend on expensive instrumentation however, it lacks real-time observation, and requires subsequent manipulation. For this reason, fluorescence is the usual method of detection of the sensitized excitation of the acceptor. If it is possible to excite the donor without exciting the acceptor, then the rate of photolysis of the acceptor (which is an excited state reaction) can be used to calculate the FRET efficiency [122],... [Pg.58]

As an analyst you understand the meaning of the scientific data you produce. However, it must be remembered that laymen often do not and so the data need to be documented in a form that is easily understood. For example, the chromatographic analysis of hydrocarbon oil from an oil spill can produce a chromatogram with over 300 components. Explaining the significance of such data to a jury will be of little benefit. However, overlaying it with a standard trace can demonstrate pictorially whether there is a similarity or not. The customer requires information from the analyst to prove a point. If the data are not fully documented, then the point cannot be proven. A customer who has confidence in a laboratory will always return. [Pg.7]

The methyl-[14C]-dimethyltin chloride was used to compare the performance of packed and megabore capillary columns in a gas chromatographic analysis for separating mixtures of a carbon-14 labelled trimethyllead chloride, tetramethyltin, dimethyltin dichloride and methyltin trichloride. The megabore column was able to separate all four methyltin compounds quickly, i.e., before the tetramethyltin decomposed into trimethyltin chloride and dimethyltin dichloride (equation 47), a reaction which did occur on the packed columns. Thus, the megabore column enabled the determination of the precise distribution of the various methyltin compounds in an environmental sample. The packed columns, on the other hand, could not separate dimethyltin dichloride and the methyltin trichloride and allowed significant decomposition of the tetramethyltin during the 15 minutes the analysis required. [Pg.783]

One of the most powerful methods for determining enantiomer composition is gas or liquid chromatography, as it allows direct separation of the enantiomers of a chiral substance. Early chromatographic methods required the conversion of an enantiomeric mixture to a diastereomeric mixture, followed by analysis of the mixture by either GC or HPLC. A more convenient chromatographic approach for determining enantiomer compositions involves the application of a chiral environment without derivatization of the enantiomer mixture. Such a separation may be achieved using a chiral solvent as the mobile phase, but applications are limited because the method consumes large quantities of costly chiral solvents. The direct separation of enantiomers on a chiral stationary phase has been used extensively for the determination of enantiomer composition. Materials for the chiral stationary phase are commercially available for both GC and HPLC. [Pg.26]

Micellar electrokinetic capillary chromatography with photodiode array detection was used for the determination of polyaromatic hydrocarbons in soil [65]. A detection limit of lOpg and linear calibration over five orders were observed. Compared to a standard gas chromatographic analysis method, the miscellar electrokinetic chromatographic method is faster, has a higher mass sensitivity and requires smaller sample sizes. [Pg.134]

Gas Chromatographic Analysis. We used temperature programmed glass capillary gas chromatography to separate PCB residues. Use of an electron capture detector required an efficaceous sample cleanup for isomer quantitation (27). These combined techniques offered enhanced separations and enabled us to identify and quantitate individual PCB constituents (jL> 27). Schwartz (27) separated more than 100 constituents from a 1 1 1 1 mixture of Aroclors 1242, 1248, 1254, and 1260. [Pg.197]


See other pages where Chromatographic analysis, requirements is mentioned: [Pg.465]    [Pg.235]    [Pg.522]    [Pg.37]    [Pg.465]    [Pg.235]    [Pg.522]    [Pg.37]    [Pg.69]    [Pg.115]    [Pg.446]    [Pg.9]    [Pg.167]    [Pg.407]    [Pg.141]    [Pg.721]    [Pg.58]    [Pg.164]    [Pg.570]    [Pg.135]    [Pg.182]    [Pg.187]    [Pg.432]    [Pg.461]    [Pg.510]    [Pg.63]    [Pg.216]    [Pg.81]    [Pg.78]    [Pg.328]    [Pg.289]    [Pg.77]    [Pg.370]    [Pg.478]    [Pg.137]    [Pg.1]    [Pg.11]    [Pg.264]    [Pg.351]    [Pg.18]    [Pg.129]   
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Chromatographic analysis

Requirement analysis

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